CN101557929B - Stretchable sheet and process for producing the stretchable sheet - Google Patents
Stretchable sheet and process for producing the stretchable sheet Download PDFInfo
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- CN101557929B CN101557929B CN200780045872.8A CN200780045872A CN101557929B CN 101557929 B CN101557929 B CN 101557929B CN 200780045872 A CN200780045872 A CN 200780045872A CN 101557929 B CN101557929 B CN 101557929B
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Abstract
Description
技术领域 technical field
本发明涉及将弹性长丝和无纺布复合化而成的伸缩片材及其制造方法。 The present invention relates to a stretch sheet made by compounding elastic filaments and non-woven fabric and its manufacturing method. the
背景技术 Background technique
作为将具有弹性的纤维与无纺布复合化而成的伸缩片材相关的现有技术,例如已知有专利文献1和2记载的技术。如这些文献的图1所示,这些文献中记载的伸缩片材由第1无纺布层122、第2无纺布层126和位于两无纺布层之间的弹性体层124构成。弹性体层124由平纹棉麻织物(scrim)、穿孔薄膜、弹性体织布、无纺布构成。在这些文献的图1中,记载了弹性体层124由弹性体平纹棉麻织物130构成,该弹性体平纹棉麻织物130由相互垂直的大量第1股线125和大量第2股线127构成。由于弹性体层124形成这样的结构,因此专利文献1和2记载的伸缩片材,当使其沿某一方向伸长时,会出现与伸长方向垂直方向的片材宽度变窄的现象,即出现宽度减缩的现象。因此,将该伸缩片材例如作为短裤型尿布的外包装材料使用时,材料沿腰身方向被拉伸,在尿布的长度方向上发生宽度减缩,因此尿布变得容易偏移掉落,或尿布上出现皱褶。另外,考虑到尿布的构成和使用者的动作,其在宽度方向上引起不均匀的伸长,因此宽度减缩变得更加明显。此外,股线125、127与无纺布层122、126是通过热及压力而接合在一起的,因此,股线125、127陷入无纺布层122、126内,从而有损无纺布层122、126的膨松感。股线125、127与无纺布层122、126是通过从无纺布122或126侧施加的热及压力而接合在一起的,因此粘接时,外侧的无纺布侧的温度容易升高,容易变成股线侧的温度比无纺布的温度低的状态。因此,如果想要获得充分的接合强度,则存在无纺布由于热及压力比股线先融化而薄膜化的问题。另外,由于需要将与股线相接触的内部纤维的树脂融化,因此要施加更高的温度或压力,从而存在使手感变差的问题。如果使用熔点高的无纺布,则无纺布纤维本身不会融化,但变得与弹性体平纹棉麻织物难以熔融粘合,因此作成片材时的 剥离强度下降。另外,高熔点的无纺布很难获得柔软的手感良好的片材。 As prior art related to a stretch sheet in which elastic fibers are combined with a nonwoven fabric, techniques described in Patent Documents 1 and 2 are known, for example. As shown in Fig. 1 of these documents, the stretch sheet described in these documents is composed of a first nonwoven fabric layer 122, a second nonwoven fabric layer 126, and an elastic body layer 124 positioned between the two nonwoven fabric layers. The elastomer layer 124 is made of scrim, perforated film, elastomer woven fabric, or nonwoven fabric. In Fig. 1 of these documents, it is described that the elastic body layer 124 is composed of an elastic body scrim 130, and the elastic body scrim 130 is composed of a large number of first strands 125 and a large number of second strands 127 perpendicular to each other. . Since the elastic body layer 124 forms such a structure, when the elastic sheet described in Patent Documents 1 and 2 is stretched in a certain direction, the width of the sheet in the direction perpendicular to the stretching direction becomes narrow. That is, the phenomenon of width reduction occurs. Therefore, when the stretchable sheet is used as an outer wrapping material for a pants-type diaper, the material is stretched in the waist direction, and the width decreases in the longitudinal direction of the diaper, so that the diaper becomes easy to fall off, or the diaper falls off easily. Creases appear. In addition, it causes uneven elongation in the width direction in consideration of the configuration of the diaper and the user's motion, so width reduction becomes more conspicuous. In addition, the strands 125, 127 and the non-woven fabric layers 122, 126 are bonded together by heat and pressure, so the strands 125, 127 are trapped in the non-woven fabric layers 122, 126, thereby damaging the non-woven fabric layers. 122, 126 bulkiness. The strands 125, 127 and the nonwoven fabric layers 122, 126 are bonded together by heat and pressure applied from the nonwoven fabric 122 or 126 side, so the temperature on the outer nonwoven fabric side tends to rise during bonding. , tends to be in a state where the temperature on the strand side is lower than the temperature of the nonwoven fabric. Therefore, if it is desired to obtain sufficient bonding strength, there is a problem that the nonwoven fabric melts before the strands due to heat and pressure and becomes thinner. In addition, since it is necessary to melt the resin of the inner fibers in contact with the strands, a higher temperature or pressure is applied, resulting in a problem that the texture is deteriorated. If a non-woven fabric with a high melting point is used, the non-woven fabric fiber itself will not melt, but it will become difficult to melt and bond with the elastic scrim, so the peel strength when it is made into a sheet will decrease. In addition, it is difficult to obtain a soft sheet with a good touch from a nonwoven fabric with a high melting point. the
作为伸缩片材的其它技术,还已知有专利文献3记载的技术。该文献中记载的伸缩片材如该文献的图1、图2和图7所示那样,通过具有齿轮形状的波形部件20、21,在片材12上形成大量的拱形部分13,在该拱形部分13的顶部(底部)上熔融粘合有弹性股线16。弹性股线16是从口模22以熔融状态被挤出,并以未拉伸的状态与片材12熔融粘合。因此,弹性股线16与片材12以点接触接合,由此,要提高接合强度并不容易。另外,该文献记载的伸缩片材的拱形部分13在变平以后再也不能伸长,有所谓的伸长极限。进而,形成拱形部分13并使片材12松弛的部分的片材12的使用量变多,并不经济,透气性也降低。另外,在该文献中记载了也可以将与弹性股线16接合前的片材12在以其坯料卷状态已经能伸长的状态下与该弹性股线接合。但是,将沿移动方向可伸长的无纺布在不使其伸长的状态下进行搬送是困难的。而且,在将专利文献3记载的伸缩片材卷绕成卷筒状时,会发生应力松弛,即由于以因卷绕时的张力而被拉伸的状态长时间保存时收缩力逐渐降低,由此在保存性方面存在问题。在另外不同的场所实施对该片材的后加工时,如果考虑到操作性和输送性,则必须将伸缩片材卷绕成卷筒状。
The technique described in patent document 3 is also known as another technique of a stretch sheet. As shown in Fig. 1, Fig. 2 and Fig. 7 of this document, the elastic sheet described in this document forms a large number of
专利文献3记载的弹性片材状复合材料是在由无纺布等构成的片材的一个表面上将弹性股线按照相互不交叉地沿一个方向延伸的方式排列而成的,所述弹性股线由冷却时具有弹性的熔融热塑性材料(例如弹性体系聚酯、聚氨酯、聚苯乙烯-聚异戊二烯-聚苯乙烯、聚苯乙烯-聚丁二烯-聚苯乙烯或者聚苯乙烯-聚(乙烯-丁烯)-聚苯乙烯)构成。这种大量长丝相互不交叉地沿一个方向延伸地排列而成的伸缩片材如下制造:从在与片材的搬送方向垂直的上隔开规定间隔排列的大量纺丝喷嘴中挤出熔融状态的长丝,并使其与所述片材熔融粘合。 The elastic sheet-like composite material described in Patent Document 3 is formed by arranging elastic strands on one surface of a sheet made of nonwoven fabric or the like so as to extend in one direction without intersecting each other. The thread is made of a molten thermoplastic material that is elastic when cooled (e.g. elastomeric polyester, polyurethane, polystyrene-polyisoprene-polystyrene, polystyrene-polybutadiene-polystyrene or polystyrene- Poly(ethylene-butylene)-polystyrene). Such a stretchable sheet in which a large number of filaments are arranged extending in one direction without intersecting each other is produced by extruding a molten state from a large number of spinning nozzles arranged at predetermined intervals perpendicular to the conveying direction of the sheet. The filaments are melt bonded to the sheet. the
但是,在上述伸缩片材的制造方法中,从纺丝喷嘴中以熔融状态挤出的长丝在与片材熔融粘合之前,有时由于风或静电等的影响而发生曲折。结果出现下述问题:本来应该在最终产品上沿一个方向直直地延伸的长丝以曲折的状态接合到片材上,从而无法制造大量的长丝等间隔地排列而成的伸缩片材。长丝的曲折可以通过将从纺丝喷嘴中挤出的长丝以规定以上的张力进行牵拉来防止,如果将对防止曲折有效的程度的张力施加到熔融状态的长丝上, 则有时该长丝会断裂(断丝),从而无法进行长丝的纺丝成形。特别是长丝的直径较细时,由于牵拉而发生断丝的情况很多,伸缩片材的生产率降低变得严重。另一方面,从提高伸缩片材的手感等观点出发,有期望长丝的直径比市售的尿布等吸收性物品所使用的弹性丝更细的倾向。 However, in the above-mentioned method for producing a stretchable sheet, filaments extruded in a molten state from a spinning nozzle may be bent by wind or static electricity before being fused with the sheet. As a result, there is a problem that filaments that should extend straight in one direction on the final product are joined to the sheet in a zigzag state, and a stretchable sheet in which a large number of filaments are arranged at equal intervals cannot be produced. The meandering of the filament can be prevented by pulling the filament extruded from the spinning nozzle at a tension greater than or equal to a specified value. If a tension effective for preventing meandering is applied to the molten filament, sometimes the The filaments are broken (broken), and spinning of the filaments cannot be performed. In particular, when the diameter of the filament is small, the filament breakage often occurs due to pulling, and the productivity of the stretchable sheet decreases seriously. On the other hand, from the viewpoint of improving the texture of the stretch sheet, the diameter of the filament tends to be thinner than that of the elastic yarn used in commercially available absorbent articles such as diapers. the
专利文献4中记载了下述方法:成形弹性股线后,使该弹性股线以经冷却固化的状态伸长,然后与无纺布接合,从而获得伸缩片材。通过弹性股线的伸长部分回复,无纺布松弛,从而在其长度范围内表现出伸缩性。由于弹性股线在与无纺布接合前被冷却固化,因此需要用粘接剂等进行与无纺布的贴合。因此,为了获得充分的粘接强度,需要较多量的粘接剂。如果较多地涂布粘接剂,则会填住无纺布纤维间的空隙,因此透气性下降。另外,由于用粘接剂将多根纤维束在一起,因此刚性提高。因而,难以获得柔软且透气性好的片材。另外,该文献中记载的伸缩片材与以使弹性丝伸长的状态贴合的通常的线状橡胶弹性体具有同样的结构,因此在伸缩片材上形成褶裥,肌肤触感差,不具有像布一样的外观。在形成了褶裥的状态下,无纺布要伸长到原来的状态,而弹性体是伸长了的状态,从而发生应力松弛,即由于以伸长的状态长时间保存而收缩力逐渐下降,因此长期保存时伸缩力降低。另外,在与无纺布等复合化的工序中,使用辊使弹性股线伸长或使其裹在辊上进行搬送时,存在着所述弹性股线粘在所述辊上、或发生断丝等问题。 Patent Document 4 describes a method of forming an elastic strand, elongating the elastic strand in a cooled and solidified state, and bonding the elastic strand to a nonwoven fabric to obtain a stretch sheet. By recovering the elongated portions of the elastic strands, the nonwoven relaxes, thereby exhibiting stretchability throughout its length. Since the elastic strand is cooled and solidified before bonding to the nonwoven fabric, it is necessary to bond the elastic strand to the nonwoven fabric with an adhesive or the like. Therefore, in order to obtain sufficient adhesive strength, a relatively large amount of adhesive is required. If a large amount of adhesive is applied, the gaps between the fibers of the nonwoven fabric will be filled, so the air permeability will decrease. In addition, since a plurality of fibers are bundled together with an adhesive, rigidity is improved. Therefore, it is difficult to obtain a soft and air-permeable sheet. In addition, the elastic sheet described in this document has the same structure as a normal linear rubber elastic body bonded in a stretched state of the elastic thread, so gathers are formed on the elastic sheet, which has poor skin feel and no Cloth-like appearance. In the state where the pleats are formed, the non-woven fabric is stretched to its original state, while the elastic body is stretched, and stress relaxation occurs, that is, the shrinkage force gradually decreases due to long-term storage in the stretched state. , so the stretching force decreases during long-term storage. In addition, in the process of compositing with non-woven fabrics, etc., when the elastic strand is stretched using a roll or wrapped on a roll for conveyance, the elastic strand may stick to the roll or break. silk and other issues. the
另外,由于该弹性体的股线都变得比较粗,因此具有坚硬的触感,手感并不好。 In addition, since the strands of the elastomer are relatively thick, it has a hard touch, which is not good in hand. the
与以上技术不同,还提出了下述弹性伸缩性复合片材:其是将由弹性伸缩性的薄膜或弹性伸缩性的连续纤维构成的弹性片材、和具有非弹性的伸长性的纤维集合体进行层叠而成的(参见专利文献5)。弹性片材和纤维集合体通过间断地配置的接合部而接合在一起。纤维集合体的构成纤维是在接合部之间连续的长纤维。该长纤维在接合部之间既不熔敷也不熔融粘合,而是纤维相互分开独立。另外,该长纤维在接合部之间呈现不规则的曲线状。 Different from the above techniques, an elastically stretchable composite sheet has also been proposed: an elastic sheet made of an elastically stretchable film or elastically stretchable continuous fibers, and an aggregate of non-elastically extensible fibers laminated (see Patent Document 5). The elastic sheet and the fiber aggregate are joined together by discontinuously arranged joints. The constituent fibers of the fiber aggregate are continuous long fibers between joints. The long fibers are neither welded nor melt-bonded between joints, but the fibers are separated and independent from each other. In addition, the long fibers have an irregular curved shape between joints. the
根据专利文献5,在该弹性伸缩性复合片材中,纤维集合体的长纤维在接合部之间呈现不规则的曲线状,因此,使该片材伸长时,其伸长不会被该纤维集合体妨碍。但是,由于纤维集合体的长纤维在接合部之间相互分开独立,因此该弹性伸缩性复合片材对牵拉的强度低。而且,纤维集合体和弹性片材 之间的剥离强度也低。另外,在接合部之间容易产生长纤维的浮起,由此片材呈起毛样的外观,外观的印象并不好。 According to Patent Document 5, in the elastically stretchable composite sheet, the long fibers of the fiber aggregates form irregular curves between joints, so that when the sheet is stretched, the elongation will not be affected by the stretch. Fibrous aggregates hinder. However, since the long fibers of the fiber aggregate are separated and independent from each other at the joints, this elastically stretchable composite sheet has low strength against pulling. Furthermore, the peel strength between the fiber assembly and the elastic sheet was also low. In addition, the floating of the long fibers tends to occur between the joints, and the sheet has a fluffy appearance, which is not a good impression of the appearance. the
专利文献1:WO00/20206A1 Patent Document 1: WO00/20206A1
专利文献2:WO00/20207A1 Patent Document 2: WO00/20207A1
专利文献3:WO95/34264A1 Patent Document 3: WO95/34264A1
专利文献4:WO01/87214A1 Patent Document 4: WO01/87214A1
专利文献5:US6730390B1 Patent Document 5: US6730390B1
发明内容 Contents of the invention
本发明提供一种伸缩片材,其中,按照相互不交叉地沿一个方向延伸的方式排列的大量弹性长丝在其整个长度上以实质上未伸长的状态与可伸长的无纺布接合。 The present invention provides a stretchable sheet in which a large number of elastic filaments arranged in such a manner as to extend in one direction without intersecting each other are bonded to an extensible nonwoven fabric in a substantially unstretched state over the entire length thereof . the
另外,本发明提供一种伸缩片材的制造方法,其中,将从纺丝喷嘴中纺出的熔融状态的大量的弹性长丝以规定速度牵拉并进行拉伸,并且在该弹性长丝固化之前,按照所述弹性长丝相互不交叉地沿一个方向排列的方式使该弹性长丝与无纺布熔融粘合,然后将熔融粘合有该弹性长丝的复合体沿着该弹性长丝的延伸方向进行拉伸,从而使该复合体具有伸缩性。 In addition, the present invention provides a method for producing a stretchable sheet, wherein a large number of elastic filaments in a molten state spun from a spinning nozzle are drawn and stretched at a predetermined speed, and the elastic filaments are solidified Before, the elastic filaments are melt-bonded with the non-woven fabric in such a way that the elastic filaments are arranged in one direction without intersecting each other, and then the composite body melt-bonded with the elastic filaments is bonded along the elastic filaments. Stretching in the direction of extension, so that the composite has stretchability. the
另外,本发明为一种伸缩片材的制造方法,其是将从纺丝喷嘴中纺出的熔融状态的大量的弹性长丝以规定速度牵拉并进行拉伸,并且在该弹性长丝固化之前,按照所述弹性长丝相互不交叉地沿一个方向排列的方式使弹性长丝与无纺布熔融粘合,然后将熔融粘合有该弹性长丝的复合体沿着该弹性长丝的延伸方向进行拉伸,从而使该复合体具有伸缩性,其中,在从所述纺丝喷嘴中纺出的所述弹性长丝与所述无纺布接触之前,该弹性长丝从该纺丝喷嘴的顶端起算的移动距离为600mm以下。 In addition, the present invention is a method for producing a stretch sheet, which comprises drawing and stretching a large number of elastic filaments in a molten state spun from a spinning nozzle at a predetermined speed, and solidifying the elastic filaments. Before, the elastic filaments are melt-bonded with the non-woven fabric in such a way that the elastic filaments are arranged in one direction without intersecting each other, and then the composite with the elastic filaments is melt-bonded along the direction of the elastic filaments. The stretching direction is stretched so that the composite has stretchability, wherein, before the elastic filaments spun from the spinning nozzle contact the nonwoven fabric, the elastic filaments are spun from the spinning The moving distance from the tip of the nozzle is 600 mm or less. the
附图说明 Description of drawings
图1为显示本发明伸缩片材的一个实施方式的局部剖视立体图。 Fig. 1 is a partially cutaway perspective view showing one embodiment of the stretch sheet of the present invention. the
图2(a)和(b)分别为图1所示伸缩片材中的弹性长丝沿着延伸方向的自然状态和伸长状态下的纵向截面图。 Fig. 2 (a) and (b) are longitudinal cross-sectional views of the elastic filaments in the stretch sheet shown in Fig. 1 in a natural state and in an elongated state, respectively, along the extension direction. the
图3为表示纤维的直径(截面积)以大致阶梯状变化的状态的非弹性纤 维的一个例子的SEM图像。 Fig. 3 is a SEM image of an example of an inelastic fiber showing a state in which the diameter (cross-sectional area) of the fiber changes approximately in a stepwise manner. the
图4为熔融张力的测定方法的说明图。 FIG. 4 is an explanatory diagram of a method of measuring melt tension. the
图5为表示图1所示的伸缩片材的制造中优选使用的装置的示意图。 Fig. 5 is a schematic view showing an apparatus preferably used for producing the stretch sheet shown in Fig. 1 . the
图6为示意地表示图5所示装置的主要部分的侧视图。 Fig. 6 is a side view schematically showing the main part of the device shown in Fig. 5 . the
图7为表示复合体被图5所示的装置拉伸的状态的示意图。 Fig. 7 is a schematic view showing a state in which the composite is stretched by the apparatus shown in Fig. 5 . the
图8为表示非弹性纤维被拉伸的状态的示意图。 Fig. 8 is a schematic diagram showing a state in which an inelastic fiber is stretched. the
图9为尿布偏移掉落性的评价方法的说明图。 Fig. 9 is an explanatory diagram of a method of evaluating the misplaced drop property of a diaper. the
具体实施方式 Detailed ways
以下基于本发明的优选实施方式,参照着附图对本发明进行说明。图1中示出了本发明的伸缩片材的一个实施方式的局部剖视立体图。 Hereinafter, the present invention will be described based on preferred embodiments of the present invention with reference to the drawings. FIG. 1 shows a partially cutaway perspective view of one embodiment of the stretch sheet of the present invention. the
本实施方式的伸缩片材10由第1无纺布11和第2无纺布12共计2张无纺布、以及夹持在两无纺布之间的大量弹性长丝13构成。具体而言,伸缩片材10如下构成:按照相互不交叉地沿一个方向延伸的方式排列的大量的弹性长丝13以实质上未伸长的状态与含有非弹性纤维而构成的可伸长的无纺布11、12接合。
The
伸缩片材10含有弹性树脂。弹性树脂使伸缩片材10具有伸缩性,是本发明的伸缩片材的必需成分。作为本发明的伸缩片材的构成部件的弹性长丝和可伸长的无纺布中,优选至少弹性长丝含有弹性树脂。可伸长的无纺布可以含有弹性树脂,也可以不含有弹性树脂。作为弹性树脂,可以使用例如后述的热塑性弹性体(SBS、SIS等)或橡胶等。
The
弹性长丝中弹性树脂的含量优选为40重量%以上、更优选为70~100重量%。由此,可以提高弹性树脂的改性(成形性提高、抗氧化、着色等)或提高弹性长丝与无纺布之间的接合强度。可伸长的无纺布中弹性树脂的含量优选为0~30重量%、更优选为0~10重量%。通过在无纺布中含有弹性树脂,不仅可以提高回复强度,而且也可以通过无纺布中含有的弹性树脂与弹性长丝树脂之间的相容性来提高接合强度。另外,从发硬感、肌肤触感、撕拉时的残丝、回复强度、弹性长丝与无纺布之间的接合强度等观点出发,本发明的伸缩片材中所含有的弹性树脂的单位面积重量优选为1~25g/m2,更优选为4~15g/m2。该单位面积重量通过后述的方法求得。 The content of the elastic resin in the elastic filaments is preferably 40% by weight or more, more preferably 70 to 100% by weight. Thereby, the modification of the elastic resin (improvement of formability, oxidation resistance, coloring, etc.) or the bonding strength between the elastic filament and the nonwoven fabric can be improved. The content of the elastic resin in the stretchable nonwoven fabric is preferably 0 to 30% by weight, more preferably 0 to 10% by weight. By containing the elastic resin in the nonwoven fabric, not only the recovery strength can be improved, but also the bonding strength can be improved by the compatibility between the elastic resin contained in the nonwoven fabric and the elastic filament resin. In addition, the unit of the elastic resin contained in the stretchable sheet of the present invention is from the viewpoints of stiffness, skin feel, residual yarn when pulled, recovery strength, and bonding strength between the elastic filament and the nonwoven fabric. The area weight is preferably 1 to 25 g/m 2 , more preferably 4 to 15 g/m 2 . This weight per unit area is obtained by the method mentioned later.
弹性长丝13与无纺布11之间的接合强度优选为10cN/25mm以上、更优选为20~200cN/25mm。弹性长丝13与无纺布12之间的接合强度也在上述范围内。通过使弹性长丝13与各无纺布11、12之间的接合强度在10cN/25mm以上,从而使伸缩片材10整体的一体感提高,在拉伸伸缩片材10或与其它片材接合时,可以有效地防止弹性长丝13从各无纺布11、12剥离等不良情况。另一方面,如果弹性长丝13与各无纺布11、12之间的接合强度超过200cN/25mm,则有可能使伸缩片材10的伸缩特性降低,因此优选将该接合强度的上限设为200cN/25mm。上述接合强度如下测定。
The bonding strength between the
<弹性长丝与无纺布之间的接合强度的测定方法> <Measurement method of joint strength between elastic filament and nonwoven fabric>
(1)无纺布为2张的情况 (1) When there are 2 non-woven fabrics
将伸缩片材按照在其伸缩方向上为150mm、在与该伸缩方向垂直的方向上为25mm的大小切得试验片。将该试验片在一个无纺布和另一个无纺布上沿该伸缩方向剥离约3cm。此时,弹性长丝与更牢固地接合的无纺布一起剥离。将如此剥离出一部分的试验片按其伸缩方向为拉伸方向的方式安装固定在牵拉试验机(岛津制作所制Autograph AG-1kNIS)的夹头之间(夹头间距为25mm)。将试验片以300mm/分钟的牵拉速度进行牵拉,直至夹头间距达到160mm,从而在一个无纺布和另一个无纺布上进行剥离,测量此时的剥离强度。剥离强度的测量区间是如下算出的:将夹头间距设定为35~150mm,并且当剥离强度在该测定区间中以显示极大极小点的方式摆动时,将从极大点(凸点)较大的5点的平均作为平均剥离强度。当不显示极大极小点时,算出平均剥离强度。另外,作为本发明的优选测定方法,使用岛津制作所制的Autograph AG-1KNIS作为牵拉试验机、并使用岛津制作所制的材料试验机用软件TRAPEZIUM2来进行测量,通过凸点最大5点平均,算出平均剥离强度。根据该方法,无论在显示极大极小和不显示极大极小的情况下都可以算出平均剥离强度。测量进行5次,将它们的平均值作为弹性长丝与无纺布之间的接合强度。 The stretchable sheet was cut into a test piece having a size of 150 mm in the stretching direction and 25 mm in the direction perpendicular to the stretching direction. This test piece was peeled off about 3 cm in the expansion-contraction direction on one nonwoven fabric and the other nonwoven fabric. At this point, the elastic filaments are peeled off together with the more firmly bonded nonwoven. A part of the test piece peeled off in this way was installed and fixed between the chucks of a tensile testing machine (Autograph AG-1kNIS manufactured by Shimadzu Corporation) in such a way that the expansion and contraction direction was the tensile direction (the distance between the chucks was 25 mm). The test piece was pulled at a pulling speed of 300 mm/min until the chuck distance reached 160 mm to peel one nonwoven fabric from the other nonwoven fabric, and the peel strength at this time was measured. The measurement interval of the peel strength is calculated as follows: set the distance between chucks at 35 to 150 mm, and when the peel strength fluctuates in the manner of showing a maximum and minimum point in the measurement interval, the maximum point (bump point ) The average of the larger 5 points was taken as the average peel strength. When no maximum and minimum points were displayed, the average peel strength was calculated. In addition, as a preferred measurement method of the present invention, Autograph AG-1KNIS manufactured by Shimadzu Corporation is used as a tensile testing machine, and the material testing machine software TRAPEZIUM2 manufactured by Shimadzu Corporation is used for measurement. The point average was used to calculate the average peel strength. According to this method, the average peel strength can be calculated irrespective of whether the maximum and minimum are exhibited or not. The measurement was performed 5 times, and the average value was used as the joint strength between the elastic filament and the nonwoven fabric. the
(2)无纺布为1张的情况 (2) When the non-woven fabric is 1 sheet
将试验片安装固定在牵拉试验机的夹头之间时,在一个夹头上安装固定弹性长丝,在另一个夹头上安装固定无纺布,除此以外,与上述(1)同样地进行。 When installing and fixing the test piece between the chucks of the tensile testing machine, install and fix the elastic filament on one chuck, and install and fix the non-woven fabric on the other chuck, in the same way as above (1). proceed. the
对于本实施方式的伸缩片材10,除了弹性长丝13与各无纺布11、12之间的接合强度在上述范围内以外,进一步使从伸缩片材10沿一个方向(弹性长丝13的延伸方向)伸长50%的状态向伸长方向的反方向收缩25%时的该伸缩片材10的强度(以下称为“25%回复强度”)优选相对于该伸缩片材10中含有的上述弹性树脂的每单位面积重量为1.0cN/{50mm·(g/m2)}以上、更优选为2.0~10cN/{50mm·(g/m2)}。通过使伸缩片材10的25%回复强度,相对于伸缩片材10中的弹性树脂的每单位面积重量,在上述范围内,特别是在用于一次性尿布的外包装材料等中时,在穿戴尿布时伸缩片材10以较小的外力即可容易地伸长,因此,尿布穿戴容易,且在正穿戴中的状态下由于表现出适度的回复强度,因此尿布的合身性变得良好。伸缩片材中所含有的弹性树脂的每单位面积重量的25%回复强度如下测定。
For the
<伸缩片材中所含有的弹性树脂的每单位面积重量的25%回复强度的测定方法> <Measuring method of 25% recovery strength per unit area weight of elastic resin contained in stretch sheet>
通过后述的方法求得伸缩片材的25%回复强度,然后除以另外求得的该伸缩片材中的弹性树脂的单位面积重量,由此求得伸缩片材中的弹性树脂的每单位面积重量的25%回复强度。伸缩片材中的弹性树脂的单位面积重量通过在制造该伸缩片材时的弹性树脂的加入量除以伸缩片材的面积来求得。在可以通过使用溶剂等而从伸缩片材中提取弹性树脂时,可以用下述方法求出伸缩片材的弹性树脂的单位面积重量。即,利用溶剂等从伸缩片材中提取弹性树脂,用NMR等分析求出该提取成分的成分比例。通过从该提取比例算出的弹性树脂的含量除以伸缩片材的面积,求得弹性树脂的单位面积重量。根据该方法,可以提取构成伸缩片材的弹性长丝中含有的弹性树脂,而且在构成伸缩片材的可伸长的无纺布中含有弹性树脂时,也可以提取所述无纺布中含有的所述弹性树脂,从而可以准确地测定伸缩片材中所含有的弹性树脂的单位面积重量。 The 25% recovery strength of the elastic sheet is obtained by the method described later, and then divided by the weight per unit area of the elastic resin in the elastic sheet obtained separately, thereby obtaining the weight per unit area of the elastic resin in the elastic sheet. 25% recovery strength by area weight. The weight per unit area of the elastic resin in the stretch sheet is obtained by dividing the amount of the elastic resin added in the production of the stretch sheet by the area of the stretch sheet. When the elastic resin can be extracted from the stretch sheet by using a solvent or the like, the weight per unit area of the elastic resin in the stretch sheet can be obtained by the following method. That is, the elastic resin is extracted from the stretchable sheet with a solvent or the like, and the component ratio of the extracted component is determined by analysis such as NMR. The weight per unit area of the elastic resin was obtained by dividing the content of the elastic resin calculated from the extraction ratio by the area of the stretch sheet. According to this method, the elastic resin contained in the elastic filaments constituting the stretch sheet can be extracted, and when the elastic resin is contained in the extensible non-woven fabric constituting the stretch sheet, the elastic resin contained in the non-woven fabric can also be extracted. The elastic resin, so that the weight per unit area of the elastic resin contained in the stretch sheet can be accurately measured. the
弹性长丝13与无纺布11、12之间的接合强度为10cN/25mm以上、且伸缩片材10中的弹性树脂的每单位面积重量的25%回复强度为1.0cN/{50mm·(g/m2)}以上的伸缩片材可以通过后述的制造方法来制造。在得到具有上述层间接合强度与伸缩特性之间的平衡性优异的伸缩片材方面特别重要的是,在其制造工序中,“在熔融状态的弹性长丝固化前使该弹性长丝与无纺布熔融粘合”。即,弹性长丝13与无纺布11、12通过熔融粘合而接合在一起,很大程度上有助于表现出上述接合强度和25%回复强度。弹性长丝与无纺布之间通过所述弹性长丝的熔融粘合以外的接合手段来接合的伸缩片材,例如在通过将固化后的弹性长丝与无纺布以二者重叠的状态进行加热加压而将它们一体化而成的伸缩片材中,无纺布的构成纤维在弹性长丝中的陷入不充分,因此难以兼顾上述的接合强度和25%回复强度。
The joint strength between the
为了使弹性长丝13与无纺布11、12之间的接合强度、以及伸缩片材10中的弹性树脂的每单位面积重量的25%回复强度分别在上述特定的范围内,作为具体的方法,可列举出例如下述的方法:在后述的制造方法中,1)对接合弹性长丝与无纺布时的夹持强度进行调整;2)对接合弹性长丝和无纺布时使用的一对辊间的间隙进行调整;3)对从将熔融状态的弹性长丝由纺丝喷嘴纺出时的该纺丝喷嘴的顶端到弹性长丝和无纺布之间的捏合部为止的距离进行调整等。通过进行上述1)~3)中的任一种,可以在将弹性长丝的形状保持在某种程度的状态下使弹性长丝与无纺布接合。一般来说,在像本发明这样将较细的长丝与无纺布进行接合时,与将远远宽于长丝的薄膜与无纺布进行接合的情况相比,由于长丝较细,因此接合时特别容易受到损伤。该损伤是指弹性长丝在伸缩片材的伸缩方向上的截面积减少。弹性长丝由于受到这样的损伤,因此发生伸缩片材的回复强度降低。但是,根据上述1)~3)的方法,不会产生上述的不良情况,可以使上述接合强度和25%回复强度分别处在上述特定的范围内。
In order to make the bonding strength between the
本实施方式的伸缩片材10除了弹性长丝13与各无纺布11、12之间的接合强度在上述范围内、以及伸缩片材10中的弹性树脂的每单位面积重量的25%回复强度在上述范围内之外,进一步优选弹性长丝和构成可伸长的无纺布11、12的纤维(无纺布构成纤维)之间的平均接合比例为10~60%、更优选为20~50%。该平均接合比例在上述范围内的伸缩片材具有充分的剥离强度,同时由弹性长丝与构成该无纺布的纤维之间的接合而产生的坚硬感不会变得明显,从而手感优异。另外,通过将该平均接合比例设定在上述范围内,可以使伸缩片材10的伸缩特性接近于弹性长丝13自身的伸缩特性。含有弹性树脂薄膜的通常的伸缩片材中的弹性树脂的单位面积重量为30~80g/m2(伸缩片材中的弹性树脂的每单位面积重量的25%回复强度为0.6cN/{50mm· (g/m2)}),与此相对,本发明的伸缩片材可以用更小单位面积重量的弹性树脂获得较高的25%回复强度和接合强度。
In the
为了使弹性长丝与上述无纺布构成纤维之间的平均接合比例在上述特的范围内,作为具体的方法,除了上述1)~3)的方法以外,还可列举出下述方法:4)使弹性树脂的熔融温度(成形温度)比无纺布构成纤维中熔点最低的低熔点成分的该熔点高125℃~180℃;5)使构成无纺布的纤维的纤维密度与通常的纤维密度相比较低,为0.05~0.12g/cm3等。通过像上述5)那样降低构成无纺布的纤维的纤维密度,可以在不阻碍弹性长丝与无纺布表面纤维的熔融粘合和伸缩的情况下得到回复强度高的片材。弹性长丝与构成无纺布的纤维之间的平均接合比例如下测定。 In order to make the average joining ratio between the elastic filament and the above-mentioned nonwoven fabric constituent fibers within the above-mentioned special range, as a specific method, in addition to the above-mentioned methods 1) to 3), the following methods can also be enumerated: 4 ) Make the melting temperature (forming temperature) of the elastic resin 125°C to 180°C higher than the melting point of the low-melting component with the lowest melting point in the fibers constituting the non-woven fabric; The density is relatively low, ranging from 0.05 to 0.12g/ cm3 . By reducing the fiber density of the fibers constituting the nonwoven fabric as in 5) above, a sheet with high recovery strength can be obtained without hindering the fusion bonding and stretching of the elastic filaments to the surface fibers of the nonwoven fabric. The average bonding ratio between the elastic filaments and the fibers constituting the nonwoven fabric was determined as follows.
<弹性长丝与构成无纺布的纤维之间的平均接合比例的测定方法> <Measurement method of the average bonding ratio between elastic filaments and fibers constituting nonwoven fabrics>
对于1根弹性长丝与无纺布的接合部分,在100~1000倍的倍率下对伸缩片材与伸缩方向垂直的方向的截面进行SEM观察,分别求得弹性长丝与无纺布构成纤维的接合部分沿所述弹性长丝的圆周方向的长度(所接合的周长)、以及弹性长丝与无纺布构成纤维的非接合部分沿所述弹性长丝的圆周方向的长度(未接合的周长),利用下式求出1根弹性长丝的接合比例。 For the joint part of one elastic filament and non-woven fabric, under the magnification of 100 to 1000 times, the cross-section of the stretch sheet in the direction perpendicular to the stretching direction is observed by SEM, and the fibers constituting the elastic filament and the non-woven fabric are obtained respectively. The length of the joined portion of the elastic filament along the circumferential direction of the elastic filament (joined circumference), and the length of the non-joined portion of the elastic filament and the non-woven fabric constituent fiber along the circumferential direction of the elastic filament (unjoined Circumferential length), the bonding ratio of one elastic filament was obtained by the following formula. the
1根弹性长丝的接合比例(%)={所接合的周长/(所接合的周长+未接合的周长)}×100 Bonding ratio of 1 elastic filament (%)={joined perimeter/(joined perimeter+unjoined perimeter)}×100
将各SEM观察中n=10的平均值作为弹性长丝与无纺布构成纤维的平均接合比例。 The average value of n=10 in each SEM observation was taken as the average joining ratio of elastic filaments and fibers constituting the nonwoven fabric. the
返回至图1,本实施方式的伸缩片材10由第1无纺布11和第2无纺布12共计2张无纺布、以及夹持在两无纺布之间的大量的弹性长丝13构成。各弹性长丝13与第1和第2无纺布11、12接合。第1无纺布11和第2无纺布12可以是同种无纺布,也可以是不同种无纺布。这里所说的同种无纺布是指无纺布的制造工艺、无纺布构成纤维的种类、构成纤维的纤维直径或长度、无纺布的厚度或单位面积重量等均相同的各无纺布。当上述中的至少一个不相同时即称为不同种无纺布。另外,本发明中的弹性是指下述性质:能够伸长,且从相对于原长度伸长100%的状态(长度为原长度的200%)释放力时,回复至原长度125%以下的长度。
Returning to FIG. 1 , the
各无纺布11、12均可伸长。各无纺布11、12可以在与弹性长丝13的延 伸方向相同的方向上伸长。所谓可伸长包括以下情况:(1)无纺布11、12的构成纤维自身伸长的情况;和(2)即使构成纤维自身不伸长,但在交点处结合的纤维彼此分开、或由于纤维彼此的结合等而使由多根纤维形成的立体结构发生结构性变化、或构成纤维被拉断、或纤维的松弛部分被拉伸,从而在无纺布整体上发生伸长的情况。
Each
各无纺布11、12也可以在与弹性长丝13接合前的坯料卷的状态下已经是可伸长的。或者可以是下述无纺布:虽然在与弹性长丝13接合前的坯料卷的状态下不是可伸长的,但按照在与弹性长丝13接合后变得可伸长的方式进行加工后,从而成为可伸长的无纺布。作为用于使无纺布变得可伸长的具体方法,可列举出热处理、辊间拉伸、利用齿槽或齿轮的啮入拉伸、利用拉幅机的牵拉拉伸等。鉴于后述的伸缩片材10的优选制造方法,从将使弹性长丝13与无纺布11、12熔融粘合时的所述无纺布11、12的搬送性变得良好的观点出发,优选无纺布11、12在坯料卷的状态下是不可伸长的。
The
各无纺布11、12可伸长,且含有实质上非弹性的纤维,从而实质上是非弹性的。
Each of the
各弹性长丝13在伸缩片材10的全长上是实质上连续的。弹性长丝13含有弹性树脂。各弹性长丝13按照相互不交叉地沿一个方向延伸的方式排列。但是,由于伸缩片材10的制造条件的不可避免的变动,弹性长丝13不经意地发生交叉的情况是允许的。各弹性长丝13只要相互不交叉,则可以以直线状延伸,也可以曲折地延伸。长丝相互不交叉是指几乎没有交点。如果有交点,则交点与交点之间有大量纤维,但通常在工业上,交点间存在的纤维的长度一致的情况是很少见的。如果在交点间存在的纤维的长度不同的状态下进行伸长,则只会对交点间所含的长度较短的纤维施加应力,即使配置很多纤维,也会产生很多未参与拉伸的纤维。相同重量的纤维进行比较时,纤维的交点较多的收缩力小。因此,浪费了成本。考虑到仅在纵向上伸缩的情况,在像网状那样在横向上存在纤维时,横向的纤维不仅变得没用,而且产生上述交点,同样地在纵向的纤维中也产生无用的部分。弹性长丝13的延伸方向可以与第1和第2无纺布11、12在制造时的移动方向一致,也可以与无纺布11、12在制造时的移动方向垂直。当按照后述的优选制造方法来制造伸缩片材10时,弹性长丝13的延伸方向与第1和第2无纺布11、12在制造时的移 动方向一致。
Each
弹性长丝13以实质上未伸长的状态与无纺布11、12接合。这些无纺布11、12可伸长。由于弹性长丝13以未伸长的状态与无纺布11、12接合,因此本实施方式的伸缩片材10具有不会产生由伸长导致的松弛(蠕变)、即伸缩性难以降低的优点。而且,例如在使弹性长丝13伸长到2倍后与无纺布11、12贴合时,假设回复到初始的1.3倍,则从该状态只能伸长到1.54倍,但在未伸长状态下贴合时,由于使伸缩片材伸长时的初始原点不同,因此具有可以伸长到无纺布11、12的可伸长长度或伸长到弹性长丝13的最大伸长率的优点。
The
弹性长丝13在未伸长的状态下与无纺布11、12接合还具有以下优点。本实施方式的伸缩片材10例如如下制造:将实质上未伸长状态的弹性长丝13与未伸长状态的无纺布11、12接合,并暂时卷取作为坯料卷,(此时,与弹性长丝13接合了的未伸长状态的无纺布11、12为非伸缩性的),将该坯料卷送出,在另外的工序中进行拉伸加工(例如齿槽拉伸),使未伸长状态的无纺布11、12成为可伸长的无纺布。在上述坯料卷的状态下,该坯料卷是未伸长且非伸缩性的,对弹性长丝13不产生外力。结果具有即使长时间保存上述坯料卷也不会发生由伸长引起的松弛的优点。
Joining of the
弹性长丝13可以是线状的合成橡胶丝或天然橡胶。或者可以是通过干式纺丝(熔融纺丝)或湿式纺丝获得的长丝。其中,鉴于后述的优选制造方法,弹性长丝13优选是不将其暂时卷取或保存而直接通过熔融纺丝获得的长丝。
The
弹性长丝13优选是将从喷嘴中喷出的熔融树脂在纺丝线上进行拉伸而获得的。通过拉伸,构成弹性长丝13的高分子沿该弹性长丝13的长度方向进行分子取向,因此,后述的50%伸长时的伸长/回复比提高,滞后损耗变小。另外,通过拉伸,可以获得细的弹性长丝。从该观点出发,弹性长丝13优选是拉伸至1.1~400倍、特别优选是拉伸至4~100倍的长丝。与此相对,在前面的专利文献3中,从口模以熔融状态挤出的弹性股线在未拉伸的状态下与片材接合,因此该弹性股线的滞后损耗不够小。另外,在专利文献4中,在进行拉伸时,由于粘附性的树脂直接接触辊,因此存在弹性股线发生缠辊的问题。
The
特别是,弹性长丝13优选是将弹性树脂在熔融或软化的状态下进行拉伸 而形成的。由此,可以得到充分细化的长丝,并由于后述的理由,手感变好。另外,通过将弹性树脂在熔融或软化的状态下进行拉伸,在贴合无纺布11、12后,达到常温的弹性长丝13不显示欲收缩的力,成为与将弹性长丝13在未伸长的状态下与无纺布11、12接合时同样的状态。作为本实施方式中拉伸的具体操作,可列举出下述操作:(1)将作为弹性长丝13原料的树脂进行熔融纺丝,先获得未拉伸丝,然后将该未拉伸丝的弹性长丝再次加热,在软化温度(硬链段部分(hard segment)的玻璃化转变温度Tg)以上的状态下进行拉伸的操作;(2)将作为弹性长丝13的原料的树脂进行熔融纺丝,将所得熔融状态的纤维直接进行拉伸的操作。如果按照后述的优选制造方法来制造伸缩片材10,则弹性长丝13可以通过将熔融纺丝后得到的熔融状态的纤维直接进行拉伸而获得。
In particular, the
通过纺丝后的拉伸获得的弹性长丝13优选其直径为10~200μm、特别优选为20~130μm。该范围是考虑伸缩片材10的手感和弹性长丝13的生产率而确定的。详细来说,如果弹性长丝13的直径过大,则接触伸缩片材10时容易感觉到由弹性长丝13带来的高度差。该高度差对伸缩片材10的手感起负作用。从该观点出发,弹性长丝13的直径越小,越容易仅感觉到各无纺布11、12的手感,因此优选。另外,通过使无纺布的透光性减少,可以具有所谓体液颜色的掩蔽功能,从该意义上来说,也优选弹性长丝13较细。另外,在后述利用齿槽辊进行的弹性表现处理中,通过使弹性长丝13的直径在齿槽辊间的齿与齿的间隙以下(作为优选的间隙,从提高齿的耐久性的观点和提高由啮入量决定的拉伸倍率的观点出发,间隙变小,为250μm以下,更优选为200μm以下),在拉伸时弹性长丝不易受到损伤(龟裂或断裂),因此优选较细。弹性长丝的直径与上述间隙之比优选为0.2~1、特别优选为0.2~0.5。尤其是,弹性长丝13的直径越细,其制造变得越容易。考虑到这些,弹性长丝13的直径优选在上述范围内。
The
从不产生上述的高度差的观点出发,弹性长丝13在伸缩片材的厚度方向上的直径相对于伸缩片材10的厚度的比例优选为1~30%、特别优选为5~12%。
The ratio of the diameter of the
弹性长丝13的截面可以是圆形,根据不同情况也可以是椭圆形或扁平形状的截面。例如按照后述的制造方法来制造伸缩片材10时,弹性长丝13的 截面有易于变为扁平形状的倾向。此时,在伸缩片材10中,弹性长丝13优选如下配置:扁平形状的长轴与伸缩片材10的平面方向大致为同方向,且短轴与伸缩片材10的厚度方向大致为同方向。
The cross section of the
弹性长丝13的截面为扁平形状时,从伸缩特性、弹性长丝13与无纺布11、12的构成纤维之间的接合强度、以及伸缩片材10的掩蔽功能增加的观点出发,长轴/短轴的比例(平均扁平率)优选为1.0~7.0、特别优选为1.1~3.0。截面为扁平形状的弹性长丝13按照其长轴方向与伸缩片材10的平面方向大致一致的方式配置。另外,弹性长丝13的截面为扁平形状时,弹性长丝13的直径是指长轴直径和短轴直径的平均。具有扁平形状的弹性长丝13中的长轴是指,通过显微镜观察选出的弹性长丝13的外周中最长正交线的长度。弹性长丝13中的短轴是指,描绘具有与如上确定的长轴平行的两边、且与上述外周外切的长方形时的短边的长度。对任意的5点弹性长丝测定上述值,将扁平率的平均值作为平均扁平率,将直径值的平均值作为弹性长丝的直径值。
When the cross section of the
弹性长丝13还优选着色为与第1和第2无纺布11、12的颜色不同的颜色。由此可以达到下述图案设计效果:弹性长丝13可以透过第1无纺布11和/或第2无纺布12看见,且伸缩片材10呈现条纹花样。这样的效果特别在各无纺布的厚度和单位面积重量在后述的范围内时变得更加显著。
The
从伸缩片材10表现出充分的伸缩性的观点、表现出像布一样的良好手感的观点、以及从根据需要表现出上述图案设计效果的观点出发,相邻的弹性长丝13的间距(相邻弹性长丝13之间的距离),以该弹性长丝13的直径在上述范围内为条件,优选为0.1~5mm、特别优选为0.4~1mm。
From the viewpoint that the
弹性长丝13在其整个长度上与各无纺布11、12接合。换言之,弹性长丝13与各无纺布11、12之间的接合部在该弹性长丝13的长度方向的全长上连续地形成。这里,“在其整个长度上接合”是指,与弹性长丝13接触的所有纤维(无纺布11、12的构成纤维)不需要与该弹性长丝13接合,而是以在弹性长丝13上不存在有意形成的非接合部的形态,将弹性长丝13与无纺布11、12的构成纤维接合。通过使弹性长丝13在其整个长度上与各无纺布11、12接合,可以充分提高弹性股线13与各无纺布11、12之间的接合力。结果,即使拉伸伸缩片材10,也难以将弹性长丝13从各无纺布11、12剥离。如果弹性长丝13从各无纺布11、12剥离,则在自然状态(松弛状态)下, 在弹性长丝13与各无纺布11、12之间产生浮起,容易在伸缩片材10上产生皱褶,从而缺少作为伸缩片材10整体的一体感。
The
作为弹性长丝13与第1和第2无纺布11、12的接合样式,可列举出例如熔融粘合等。如果按照后述的优选制造方法来制造伸缩片材10,则弹性长丝13通过熔融粘合与各无纺布11、12接合。所谓熔融粘合,包括弹性长丝与构成无纺布11、12的纤维相互熔融而粘接的状态,或者任意一方熔融、另一方陷入其中而粘接的状态这两种。根据该方法,可以在不对各无纺布11、12施加过度的热的情况下,在通过熔融纺丝获得的弹性长丝13的固化之前,使该弹性长丝13与无纺布熔融粘合,因此仅是在该弹性长丝13的周围存在的纤维与该弹性长丝13接合,而远离该位置的纤维维持着无纺布11、12的手感,因此具有伸缩片材10的手感得以良好保持的优点。此时,在各无纺布11、12与弹性长丝13接合前,作为辅助的接合手段,还可以涂布粘接剂。或者,在各无纺布11、12与弹性长丝13接合后,作为辅助的接合手段,还可以进行热处理(蒸汽喷射、热压花)或机械交织(针刺法、射流喷网法)等。但是这些辅助的接合手段有时会损害所得伸缩片材10的手感,或对弹性长丝13造成损伤。因此,优选将弹性长丝13通过其熔融热与无纺布11、12熔融粘合。但是,作为辅助接合手段,当使用由利用热风法的热风吹附形成的热处理时,可以在不损害所得伸缩片材10的手感的情况下仍获得无纺布11、12的接合强度高的片材,从该点出发是优选的。
As a joining form of the
伸缩片材10可以在与弹性长丝13的延伸方向相同的方向上伸缩。伸缩片材10的伸缩性由于弹性长丝13的弹性而表现出来。当将伸缩片材10在与弹性长丝13的延伸方向相同的方向上拉伸时,弹性长丝13以及第1和第2无纺布11、12伸长。然后释放伸缩片材10的拉伸时,弹性长丝13收缩,随着其收缩,第1和第2无纺布11、12回复到拉伸前的状态。
The
与前述专利文献1和2中记载的片材不同,在本实施方式的伸缩片材10中,以与弹性长丝13垂直的状态结合的其它弹性长丝并不存在。因此,即使将伸缩片材10在与弹性长丝13的延伸方向相同的方向上拉伸,该伸缩片材10也会在基本不发生宽度减缩的情况下伸长。即,伸缩片材10在其拉伸状态下,在其长度方向上宽度是大致一样的。结果,在将伸缩片材10以其伸长状态搬送并对其进行加工时,操作性变得良好。另外,在将伸缩片材10作为例 如短裤型尿布的外包装材料使用时,可以有效地防止尿布在戴用过程中发生偏移掉落或发生皱褶。另外,如果考虑到尿布的构成和使用者的动作,虽然在宽度方向上发生不均匀的伸长,但此时也基本不会发生宽度减缩,可以有效地防止尿布偏移或发生皱褶。从该观点出发,将伸缩片材10伸长到1.5倍时的宽度减缩比例优选为伸长前的宽度的1%~10%、特别优选为1%~5%。宽度减缩可以用(1-伸长后的宽度÷伸长前的宽度)×100来求出。伸长后的宽度如下测定。将样品按照其长度方向大致沿着移动方向的方式(角度差为15度以内)按宽度50mm裁切。长度超过150mm。在将样品的宽度保持在50mm的状态下,将样品的长度方向两端部以把持间隔为150mm进行把持。此时,注意要使样品在其长度方向上不松弛也不伸长。从该状态开始,将把持间隔拉伸到1.5倍,测定此时的样品的长度方向中央部的宽度,将该值作为伸长后的宽度。
Unlike the sheets described in the aforementioned Patent Documents 1 and 2, in the
图2(a)和(b)示出了本发明的一个实施方式的伸缩片材10中沿着弹性长丝13的延伸方向的纵向截面图。图2(a)和(b)中示出的实施方式是在伸缩片材10的制造工序中的弹性表现处理中,使用齿槽拉伸时显著表现出的形态。图2(a)是自然状态(松弛状态)下的伸缩片材10的纵向截面图,图2(b)是伸长状态下的伸缩片材10的纵向截面图。在自然状态下,伸缩片材10呈顶部14′和谷部14″交替排列的波浪形状。顶部14′和谷部14″通过棱线部15′相连。相对于顶部14′和谷部14″的厚度,棱线部15′的厚度稍小一些,因此比顶部14′和谷部14″更容易透光。俯视伸缩片材10时,顶部14′、棱线部15′以及谷部14″向着与伸缩片材10的伸长方向垂直的方向延伸。因此,在伸缩片材10中,在其自然状态下,由容易透光的棱线部15′和与比其难以透光的顶部14′和谷部14产生的横向条纹花样隐约出现。该横向条纹花样会由于伸缩片材10伸长和后述的弹性表现处理等条件而变得更加明显。
2( a ) and ( b ) show longitudinal cross-sectional views along the extending direction of the
即,如图2(b)所示,在伸长状态的伸缩片材10中,沿着弹性长丝13的延伸方向,高单位面积重量部分14和低单位面积重量部分15交替排列。各部分14、15在与弹性长丝13的延伸方向垂直的方向上分别以带状延伸。高单位面积重量部分14和低单位面积重量部分15以恒定的周期交替排列。对于高单位面积重量部分14,向片材10的上侧突出的部分和向片材10的下侧突出的部分交替配置。向片材10的上侧突出的高单位面积重量部分14来 自于图2(a)所示的自然状态的片材10中的顶部14′。而向片材10的下侧突出的高单位面积重量部分14来自于图2(a)所示的自然状态的片材10中的谷部14″。另外,低单位面积重量部分15来自于图2(a)所示的自然状态的片材10中的棱线部15′。在高单位面积重量部分14与低单位面积重量部分15中,由于它们的单位面积重量差而在透光程度上存在差异。结果,伸缩片材10呈现在与弹性长丝13的延伸方向垂直的方向上延伸的横向条纹花样,图案设计性高。特别是,如前所述,伸缩片材10也呈现由弹性长丝13产生的条纹花样,因此伸缩片材10还呈现该条纹花样与由高单位面积重量部分14和低单位面积重量部分15产生的条纹花样的组合而成的格子状的花样,图案设计性进一步提高。另外,如图2(a)和(b)所示,作为本发明的优选实施方式,片材10的上侧或下侧的突出的部分中填充着纤维。
That is, as shown in FIG. 2( b ), in the stretched
高单位面积重量部分14与低单位面积重量部分15相比,单位面积重量大且厚度也大。由此,高单位面积重量部分14和低单位面积重量部分15处的透光程度不同,由于该不同而呈现条纹花样。各高单位面积重量部分14彼此间实质上是等宽度的,同样地,各低单位面积重量部分15彼此间也实质上是等宽度的。 The high basis weight portion 14 has a larger basis weight and a larger thickness than the low basis weight portion 15 . Accordingly, the light transmission degree differs between the high basis weight portion 14 and the low basis weight portion 15 , and a striped pattern appears due to the difference. The high basis weight portions 14 are substantially equal in width to each other, and similarly, the respective low basis weight portions 15 are also substantially equal in width to each other. the
高单位面积重量部分14的厚度优选为0.3~10mm、特别优选为0.5~1mm。从伸缩特性和透气性的观点出发,低单位面积重量部分15的厚度优选为0.1~3mm、特别优选为0.2~0.6mm。厚度的测定是将伸缩片材10在20±2℃、65±5%RH的环境下无负荷地放置2天以上,然后用下述方法求出。首先,将伸缩片材10向伸长方向拉伸到1.5倍,在该状态下,以0.5cN/cm2的负荷夹在平板间。用显微镜在50~200倍的倍率下观察截面,分别求出各视野中的平均厚度,以三个视野的厚度的平均值的形式求得上述厚度。高单位面积重量部分14和低单位面积重量部分15在按照后述的制造方法来制造伸缩片材10时可以容易地形成。
The thickness of the high basis weight portion 14 is preferably 0.3 to 10 mm, particularly preferably 0.5 to 1 mm. The thickness of the low basis weight portion 15 is preferably 0.1 to 3 mm, particularly preferably 0.2 to 0.6 mm, from the viewpoint of stretchability and air permeability. The thickness is measured by leaving the
下面,对构成伸缩片材10的第1和第2无纺布11、12以及弹性长丝13的构成材料进行说明。作为构成各无纺布11、12的纤维,可以使用实质上非弹性的纤维。作为其例子,可列举出聚乙烯(PE)、聚丙烯(PP)、聚酯(PET或PBT)、聚酰胺等构成的纤维等。构成各无纺布11、12的纤维可以是短纤维也可以是长纤维,可以是亲水性的也可以是疏水性的。另外,还可以使用 芯鞘型或并列型的复合纤维、分割纤维、异形截面纤维、卷曲纤维、热收缩纤维等。这些纤维可以单独使用一种,也可以组合两种以上来使用。各无纺布11、12可以是连续长丝或短纤维的无纺布。特别是,从将伸缩片材10制成有厚度的膨松的片材的观点出发,各无纺布11、12优选为短纤维的无纺布。将伸缩片材10作为与肌肤接触的部件使用时,可以在肌肤接触侧使用手感好的短纤维无纺布,在其相反面使用高强度的连续长丝的无纺布。
Next, constituent materials of the first and second
各无纺布11、12优选其构成纤维由低熔点成分和高熔点成分两个成分以上组成。此时,通过至少低熔点成分的热熔融粘合,其构成纤维彼此在纤维交点处接合。作为由低熔点成分和高熔点成分两个成分以上构成的芯鞘型的复合纤维,优选芯为高熔点的PET、PP,鞘为低熔点的PET、PP、PE。特别在使用这些复合纤维时,与弹性长丝13的熔融粘合变强,难以引起两者间的剥离,因此优选。
Each of the
各无纺布11、12的厚度优选为0.05~5mm、更优选为0.1~1.0mm、进一步优选为0.15~0.5mm。厚度的测定可以如下进行:以0.5cN/cm2的负荷夹在平板间,用显微镜在50~200倍的倍率下观察伸缩片材10的截面,分别求出各视野中的平均厚度,以三个视野的厚度的平均值的形式求出上述厚度。片材整体的厚度可以通过测量平板间的距离来求得。从手感、厚度及图案设计性等观点出发,各无纺布11、12的单位面积重量优选分别为3~100g/m2、特别优选为10~30g/m2。
The thickness of each of the
从手感、粘性等观点出发,各无纺布11、12优选由实质上非弹性的纤维构成。作为无纺布中的非弹性纤维的比例,可以为70重量%以上、优选为90重量%以上、更优选为100重量%。另外,实质上非弹性的纤维也可以在非弹性树脂中含有弹性树脂,非弹性树脂的比例可以为70重量%以上、优选为90重量%以上、更优选为100重量%。特别地,作为非弹性的纤维,优选使用在长度方向上纤维的粗细度不一样的纤维(以下将该纤维称为不定径纤维)。即,不定径纤维在沿其长度方向看时,既有纤维截面积(直径)大的部分,也有纤维截面积(直径)小的部分。在不定径纤维中,其直径(截面积)可以从最小的部分到最大的部分连续地变化。或者,也可以像在未拉伸丝的拉伸工序中观察到的缩颈现象那样,纤维的直径(截面积)以大致阶梯状变化。图3中示出了具有纤维的直径(截面积)以大致阶梯状变化的状态的非弹性纤维 的一个例子。
It is preferable that each of the
非弹性纤维以具有恒定的纤维直径的高伸长率(例如纤维的最大伸长率为80~800%、特别为120~650%)的纤维作为原料,这从可以获得最大强度高的伸缩片材10的观点出发是优选的。纤维的伸长率根据JIS L-1015,以下述条件下的测定为基准:即测定环境温湿度为20±2℃、65±5%RH,牵拉试验机的夹具间隔为20mm,牵拉速度为20mm/min。另外,以从已制造的无纺布中采集纤维来测定伸长率为代表,夹具间隔不能设在20mm时,即所测定的纤维长度不足20mm时,将夹头间隔设在10mm或5mm来进行测定。
Non-elastic fibers are made of fibers with constant fiber diameter and high elongation (for example, the maximum elongation of the fiber is 80-800%, especially 120-650%), which can obtain a stretchable sheet with high maximum strength. It is preferable from the viewpoint of
上述高伸长率的纤维优选为低拉伸的非弹性纤维。以低拉伸的非弹性纤维为原料,按照后述的制造方法来制造本实施方式的伸缩片材10时,在弹性表现处理过程中通过将低拉伸的纤维进行拉伸,可以在纤维中产生较细的部分,从而形成上述不定径纤维。结果,在本实施方式的伸缩片材的弹性表现处理过程中,无纺布变为在结构上容易拉伸的形态,通过拉伸纤维,整个无纺布结构都变得容易拉伸,将对不定径纤维间的接合点、各无纺布11、12与弹性长丝13的接合点的破坏控制在最小限,能够在维持伸缩性能的同时提高伸缩片材10的强度。即可以得到兼具高伸长率和高强度的伸缩片材10。另外,在弹性表现处理过程中上述不定径纤维间的接合也难以被破坏,这还具有使各无纺布11、12难以起毛的效果。这从提高本实施方式的伸缩片材10的外观的观点出发是有利的。与此相对,对于背景技术部分中描述的专利文献5记载的弹性伸缩性复合片材,由于在拉伸工序中构成纤维难以延伸,因此纤维彼此的熔敷或机械性的络合不能实现。结果,片材的强度降低,不能兼具高伸长率和高强度。
The aforementioned high-elongation fibers are preferably low-stretch non-elastic fibers. When the
另外,通过以上述低拉伸的纤维为原料,与纤维拉伸前相比,细纤维的根数(长度)实质上增加。由此,本实施方式的伸缩片材10的不透光性提高。从提高难以透过正面片材看到被吸收体吸收的体液的掩蔽性能的观点出发,伸缩片材10的不透光性提高在例如将伸缩片材10作为生理用卫生巾或一次性尿布等吸收性物品的正面片材使用时是有利的。
In addition, by using the above-mentioned low-drawn fiber as a raw material, the number (length) of thin fibers substantially increases compared with that before fiber drawing. Thereby, the opacity of the
此外,如果不定径纤维的粗细度周期性地变化,则还具有下述附加效果:即各无纺布11、12的表面呈现微细的波状起伏的状态,其肌肤触感变得良好。此时,变化的周期、即较粗部分与和其相邻的较粗部分之间的距离优选为0.5~ 10mm、特别优选为2~5mm。该周期可以从各无纺布11、12的显微镜观察来测定。这里,不定径纤维的直径的测定可以按照以下的(1)~(5)的顺序来测定。
In addition, if the thickness of the non-diameter fibers is periodically changed, there is an additional effect that the surfaces of the
(1)从伸缩片材10的表面上的5mm×5mm以上的区域中采样无纺布11或无纺布12。此时的样品可以将无纺布11、12从弹性长丝13上切离来采集,也可以采集伸缩片材10整体。
(1) The
(2)将采集的样品固定在SEM的观察用试样台上。此时,为了容易观察样品,也可以在以不破坏样品的结构的程度拉伸样品的状态下(直到无纺布的松弛消失的程度),将样品用双面胶固定在试样台上。对于此时的拉伸量,例如在伸缩片材10的制造工序中利用弹性表现处理工序时,使其为拉伸工序中拉伸伸缩片材10的前体的拉伸倍率以下的程度。
(2) The collected sample is fixed on the sample stage for SEM observation. At this time, in order to facilitate observation of the sample, the sample may be fixed on the sample stand with double-sided tape while stretching the sample to such an extent that the structure of the sample is not broken (to the extent that the slack of the nonwoven fabric disappears). The amount of stretching at this time is set to be equal to or less than the stretching ratio at which the precursor of the
(3)SEM观察在200的倍率下进行。使1处的视野面积为0.4mm×0.4mm左右以上,观察5处。 (3) SEM observation was performed at a magnification of 200. The field of view area at one point was about 0.4 mm×0.4 mm or more, and five points were observed. the
(4)随机地抽出纤维,以0.1μm为单位在纤维轴向上每隔10μm地测定直径,共测定20处以上(纤维彼此的熔融粘合点或破坏的部分不包括在测定中)。纤维在各视野测定4根以上,对5个视野的共计20根进行测定。 (4) Randomly extract fibers, and measure the diameter at intervals of 10 μm in the fiber axial direction in units of 0.1 μm, and measure more than 20 places in total (fusion bonding points between fibers or broken parts are not included in the measurement). Four or more fibers were measured in each visual field, and a total of 20 fibers in five visual fields were measured. the
(5)从这些值中选出20根纤维的各自的最大直径和最小直径。 (5) From these values, the respective maximum diameters and minimum diameters of 20 fibers are selected. the
1根纤维的最大直径和最小直径之差为1μm以上、对纤维轴向的位置和直径的变化之间的关系作图时,极大位置或极小位置为2处以上的纤维称为不定径纤维。 The difference between the maximum diameter and the minimum diameter of one fiber is 1 μm or more, and when the relationship between the axial position of the fiber and the change in diameter is plotted, a fiber with two or more maximum positions or minimum positions is called indeterminate. fiber. the
从使以上的各效果更显著的观点出发,不定径纤维的粗细度在最细部分处优选为2~15μm、更优选为5~12μm、在最粗部分处优选为10~40μm、更优选为12~30μm。不定径纤维的最大直径和最小直径之差优选为3μm以上、特别优选为5μm以上、尤其优选为10μm以上。另外,以“最大纤维直径/最小纤维直径”所定义的纤维直径的比值优选为1~15、更优选为1.2~10、进一步优选为2~5。 From the viewpoint of making the above effects more remarkable, the thickness of the indeterminate fiber is preferably 2 to 15 μm at the thinnest portion, more preferably 5 to 12 μm, and preferably 10 to 40 μm at the thickest portion, more preferably 12~30μm. The difference between the maximum diameter and the minimum diameter of the indeterminate fiber is preferably 3 μm or more, particularly preferably 5 μm or more, particularly preferably 10 μm or more. In addition, the ratio of the fiber diameter defined by "maximum fiber diameter/minimum fiber diameter" is preferably 1-15, more preferably 1.2-10, even more preferably 2-5. the
不定径纤维优选其纤维间熔融粘合点强度高于该不定径纤维的100%伸长时的强度。由此,在制造伸缩片材10时的弹性表现处理工序中,在将拉伸前的伸缩片材10进行拉伸以实施弹性表现处理加工时,难以引起弹性表现处理前的伸缩片材10的纤维彼此的熔融粘合点的破坏,与弹性表现前的伸缩片材10的强度相比,经过上述弹性表现处理工序获得的伸缩片材10的强度不易降低,从该点出发是优选的。熔融粘合点强度可以按照本申请人的在先申请日本特开2004-218183号公报的[0040]段落的记载来进行测定。100%伸长时的强度可以使用牵拉试验机、在夹头间距离为20mm、牵拉速度为20mm/min的条件下来进行测定。
The non-sizing fibers preferably have an interfiber fusion bond strength higher than the 100% elongation strength of the non-sizing fibers. Therefore, in the elastic expressing treatment process when the
上述的低拉伸的非弹性纤维包括:纺丝后以低拉伸倍率被拉伸的纤维以及未拉伸的纤维、即未拉伸纤维这两者。作为低拉伸的纤维,优选使用其伸长率为如上所述的80~800%的纤维、特别优选使用伸长率为120~650%的纤维。通过使用具有该范围的伸长率的低拉伸的纤维,该纤维在后述的图5所示的拉伸装置22中可以顺利地被拉伸,可以容易地形成不定径纤维。低拉伸的纤维的纤维直径优选为10~35μm、特别优选为12~30μm。
The aforementioned low-stretch non-elastic fiber includes both: a fiber drawn at a low draw ratio after spinning and an undrawn fiber, ie, an undrawn fiber. As the low-stretch fiber, it is preferable to use a fiber having an elongation of 80 to 800% as described above, and it is particularly preferable to use a fiber having an elongation of 120 to 650%. By using a low-stretch fiber having an elongation in this range, the fiber can be smoothly stretched in a stretching
如前所述,不定径纤维优选以具有恒定的纤维直径的低拉伸的纤维为原料。此时,低拉伸的纤维可以是由单一的原料构成的纤维,也可以是使用了2种以上原料的复合纤维、例如芯鞘型复合纤维或并列型复合纤维。如果考虑到不定径纤维彼此接合的容易性、各无纺布11、12与弹性长丝13的接合容易性,优选使用复合纤维。在为芯鞘型的复合纤维的情况下,优选芯为聚酯(PET或PBT)、聚丙烯(PP)、鞘为低熔点的聚酯(PET或PBT)、聚丙烯(PP)、聚乙烯(PE)。特别地,在使用这些复合纤维时,在弹性长丝13含有聚烯烃系弹性体的情况下,弹性长丝13与各无纺布11、12的构成纤维之间的热熔融粘合增强,难以引起层剥离,从该点出发是优选的。
As previously stated, non-sizing fibers are preferably derived from low-stretch fibers having a constant fiber diameter. In this case, the low-stretch fiber may be a fiber composed of a single raw material, or may be a composite fiber using two or more raw materials, such as a core-sheath composite fiber or a side-by-side composite fiber. In consideration of the ease of bonding of non-diameter fibers to each other and the ease of bonding of the
不定径纤维可以是如人造短纤维那样的短纤维,也可以是如连续长丝那样的长纤维。鉴于后述的伸缩片材10的优选制造方法,优选使用短纤维。另外,不定径纤维可以是亲水性的或疏水性的。
The indeterminate fibers may be short fibers such as staple fibers or long fibers such as continuous filaments. In view of a preferable manufacturing method of the
各无纺布11、12可以仅由不定径纤维构成,也可以除了不定径纤维以外还含有其它的恒定直径的非弹性纤维。作为其它的非弹性纤维,可列举出前述的纤维。各无纺布11、12除了不定径纤维以外还含有其它的恒定直径的非弹性纤维时,其它的非弹性纤维的配合量优选为1~30重量%、特别优选为5~20重量%。
Each of the
不定径纤维特别优选在两张无纺布11、12这二者中都含有,但也可以仅含有在两张无纺布11、12中的一个中。
It is particularly preferable that the non-caliber fibers be contained in both of the two
弹性长丝13如前所述,例如以热塑性弹性体或橡胶等弹性树脂为原料。弹性长丝13为具有弹性的长纤维。特别地,当弹性树脂使用热塑性弹性体作为原料时,可以与通常的热塑性树脂同样地使用挤出机进行熔融纺丝,而且由此得到的长丝容易热熔融粘合,因此适于本实施方式的伸缩片材。作为热塑性弹性体,可列举出SBS(苯乙烯-丁二烯-苯乙烯)、SIS(苯乙烯-异戊二烯-苯乙烯)、SEBS(苯乙烯-乙烯-丁二烯-苯乙烯)、SEPS(苯乙烯-乙烯-丙烯-苯乙烯)等苯乙烯系弹性体、烯烃系弹性体(乙烯系的α-烯烃弹性体、乙烯/丁烯/辛烯等共聚而成的丙烯系弹性体)、聚酯系弹性体、聚氨酯系弹性体。它们可以单独使用一种,也可以组合两种以上来使用。另外,也可以使用由这些树脂构成的芯鞘型或并列型的复合纤维。特别地,从弹性长丝13的成形性、伸缩特性、成本方面考虑,优选使用苯乙烯系弹性体、烯烃系弹性体、或它们的组合。
The
弹性长丝13与构成无纺布11、12的纤维的优选组合是下述组合:弹性长丝13使用SEBS树脂或SEPS树脂,无纺布11、12的构成纤维使用PP/PE芯鞘型复合纤维或PET/PE芯鞘型复合纤维。通过采用该组合,可以可靠地进行熔融粘合。另外,由于芯的熔点高,因此纤维在熔融粘合时熔融不完全(残留芯),可以得到最大强度高的伸缩片材10。
The preferred combination of the
特别地,作为弹性长丝13,优选使用由含有A1-B-A2型三嵌段共聚物而构成的树脂组合物形成的弹性长丝,所述A1-B-A2型三嵌段共聚物由以乙烯基芳香族聚合物为主体的聚合物嵌段A1和A2、和以聚烯烃为主体的聚合物嵌段B形成。
In particular, as the
聚合物嵌段A1和A2各自的通过凝胶渗透色谱法(GPC)测定的重均分子量的总计为优选为14000~20000,更优选为14000~18000,且聚合物嵌段B通过GPC法测定的重均分子量优选为40000~80000、更优选为40000~70000。在本说明书中,通过GPC法测定的重均分子量是在下述测定条件下测定的:柱:TSKgel G-2000H;柱温度:40℃;流动相:四氢呋喃(THF);流量:1.0mL/min;试样浓度:10mg/5mL-THF;注入量:500μL;然后用聚苯乙烯换算后得到上述重均分子量的值。作为分析试样,使用进行了下述前处理操作得到的试样:将试样10mg在常温下在5mL的四氢呋喃中溶解10分钟,然后用孔径为0.45μm的烧结过滤器过滤。 The sum of the weight average molecular weights of the polymer blocks A1 and A2 as measured by gel permeation chromatography (GPC) is preferably 14000 to 20000, more preferably 14000 to 18000, and the polymer block B as measured by the GPC method The weight average molecular weight is preferably 40,000 to 80,000, more preferably 40,000 to 70,000. In this specification, the weight average molecular weight determined by GPC method is determined under the following measurement conditions: column: TSKgel G-2000H; column temperature: 40°C; mobile phase: tetrahydrofuran (THF); flow rate: 1.0mL/min; Sample concentration: 10mg/5mL-THF; injection volume: 500μL; and the value of the above-mentioned weight-average molecular weight was obtained by converting polystyrene. As an analysis sample, a sample obtained by the following pretreatment operation was used: 10 mg of the sample was dissolved in 5 mL of tetrahydrofuran at room temperature for 10 minutes, and then filtered through a sintered filter with a pore size of 0.45 μm. the
在树脂组合物含有2种以上的A1-B-A2型三嵌段共聚物时,例如将上述的“聚合物嵌段A1通过GPC法测定的重均分子量”作为2种以上的A1-B-A2型三嵌段共聚物各自的聚合物嵌段A1通过GPC法测定的重均分子量的重量平均值来求得。即,例如树脂组合物含有(A1’-B’-A2’)及(A1”-B’-A2”)两种A1-B-A2型三嵌段共聚物作为A1-B-A2型三嵌段共聚物、且(A1’-B’-A2’)的百分含量(A1’-B’-A2’在树脂组合物所含的两种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)为80重量%、(A1”-B”-A2”)的百分含量为20重量%时,上述“聚合物嵌段A1通过GPC法测定的重均分子量”通过下式求得。 When the resin composition contains two or more types of A1-B-A2 type triblock copolymers, for example, the above-mentioned "weight average molecular weight of the polymer block A1 measured by GPC" is used as two or more types of A1-B- The polymer block A1 of each type A2 triblock copolymer is obtained by the weight average of the weight average molecular weight measured by the GPC method. That is, for example, the resin composition contains (A1'-B'-A2') and (A1"-B'-A2") two A1-B-A2 type triblock copolymers as A1-B-A2 type triblock copolymers. Segment copolymer, and the percentage content of (A1'-B'-A2') (A1'-B'-A2' contains two or more A1-B-A2 type triblock copolymers contained in the resin composition When the percentage content in the total amount of (A1 "-B"-A2") is 80% by weight and the percentage content of (A1"-B"-A2") is 20% by weight, the weight average of the above "polymer block A1 measured by GPC method Molecular weight" is obtained by the following formula.
(聚合物嵌段A1’的通过GPC法测定的重均分子量)×0.8+(聚合物嵌段A1”的通过GPC法测定的重均分子量)×0.2 (The weight-average molecular weight measured by the GPC method of the polymer block A1')×0.8+(the weight-average molecular weight measured by the GPC method of the polymer block A1″)×0.2
在树脂组合物含有两种以上的A1-B-A2型三嵌段共聚物时,对于上述“聚合物嵌段A2通过GPC法测定的重均分子量”及“聚合物嵌段B通过GPC法测定的重均分子量”,也分别按照聚合物嵌段A1的上述例子来求得。 When the resin composition contains two or more A1-B-A2 type triblock copolymers, for the above "weight average molecular weight of polymer block A2 measured by GPC method" and "polymer block B measured by GPC method The weight-average molecular weight of ", also obtain respectively according to the above-mentioned example of polymer block A1. the
另外,在树脂组合物含有两种以上的A1-B-A2型三嵌段共聚物时,上述“聚合物嵌段A1及A2各自通过GPC法测定的重均分子量的总计”为如上求得的聚合物嵌段A1及A2各自的上述重均分子量的重量平均值的总计。 In addition, when the resin composition contains two or more types of A1-B-A2 type triblock copolymers, the above-mentioned "total weight average molecular weight of each of the polymer blocks A1 and A2 measured by the GPC method" is obtained as above The total of the weight averages of the above-mentioned weight average molecular weights of the respective polymer blocks A1 and A2. the
弹性长丝13通过由含有满足上述物性的A1-B-A2型三嵌段共聚物而构成的树脂组合物形成,纺丝成形性优异,即使在直径较细时,也不会引起断丝,且可以无曲折地从纺丝喷嘴中喷出成形。
The
聚合物嵌段A1以乙烯基芳香族聚合物为主体构成。作为构成该乙烯基芳香族聚合物的乙烯基芳香族,可列举出例如苯乙烯、对甲基苯乙烯、间甲基苯乙烯、对叔丁基苯乙烯、α-甲基苯乙烯、氯代甲基苯乙烯、对叔丁氧基苯乙烯、二甲基氨基甲基苯乙烯、二甲基氨基乙基苯乙烯、乙烯基甲苯、1-乙烯基萘、4-丙基苯乙烯、4-环己基苯乙烯、4-十二烷基苯乙烯、2-乙基-4-苄基苯乙烯、4-(苯基丁基)苯乙烯等。乙烯基芳香族聚合物可以由这些乙烯基芳香族中的1种构成,也可以由2种以上构成。在这些乙烯基芳香族中,从聚合的容易性和通用性的观点出发,优选苯乙烯。 The polymer block A1 is mainly composed of a vinyl aromatic polymer. Examples of the vinyl aromatic constituting the vinyl aromatic polymer include styrene, p-methylstyrene, m-methylstyrene, p-tert-butylstyrene, α-methylstyrene, chlorinated Methylstyrene, p-tert-butoxystyrene, dimethylaminomethylstyrene, dimethylaminoethylstyrene, vinyltoluene, 1-vinylnaphthalene, 4-propylstyrene, 4- Cyclohexylstyrene, 4-dodecylstyrene, 2-ethyl-4-benzylstyrene, 4-(phenylbutyl)styrene, and the like. The vinyl aromatic polymer may be composed of one type of these vinyl aromatics, or may be composed of two or more types. Among these vinyl aromatics, styrene is preferable from the viewpoint of ease of polymerization and versatility. the
聚合物嵌段A1中乙烯基芳香族聚合物的含量相对于聚合物嵌段A1的整个结构单元,优选为90~100重量%、更优选为95~100重量%。 The content of the vinyl aromatic polymer in the polymer block A1 is preferably 90 to 100% by weight, more preferably 95 to 100% by weight, based on the entire structural unit of the polymer block A1. the
聚合物嵌段A1除了乙烯基芳香族聚合物以外,还可以含有共轭二烯化合物聚合物而构成。作为构成该共轭二烯化合物聚合物的共轭二烯化合物,可列举出例如1,3-丁二烯、异戊二烯、1,3-戊二烯、2,3-二甲基-1,3-丁二烯、2-甲基-1,3-戊二烯、1,3-己二烯、苯基丁二烯、4,5-二乙基-1,3-辛二烯、3-丁基-1,3-辛二烯等。共轭二烯化合物聚合物可以由这些共轭二烯化合物中的1种构成,也可以由2种以上构成。 The polymer block A1 may contain a conjugated diene compound polymer in addition to the vinyl aromatic polymer. Examples of the conjugated diene compound constituting the conjugated diene compound polymer include 1,3-butadiene, isoprene, 1,3-pentadiene, 2,3-dimethyl- 1,3-butadiene, 2-methyl-1,3-pentadiene, 1,3-hexadiene, phenylbutadiene, 4,5-diethyl-1,3-octadiene , 3-butyl-1,3-octadiene, etc. The conjugated diene compound polymer may be composed of one type of these conjugated diene compounds, or may be composed of two or more types. the
聚合物嵌段A1中共轭二烯化合物聚合物的含量是,相对于聚合物嵌段A1的整个结构单元优选为0~10重量%、更优选为0~5重量%。 The content of the conjugated diene compound polymer in the polymer block A1 is preferably 0 to 10% by weight, more preferably 0 to 5% by weight, based on the entire structural unit of the polymer block A1. the
聚合物嵌段A1的通过GPC法测定的重均分子量优选为7000~10000,更优选为7000~9000。 The weight average molecular weight measured by the GPC method of polymer block A1 becomes like this. Preferably it is 7000-10000, More preferably, it is 7000-9000. the
作为聚合物嵌段A2,可以使用与上述聚合物嵌段A1相同的嵌段。对聚合物嵌段A2没有特别说明的方面可以适当适用对聚合物嵌段A1的说明。在A1-B-A2型三嵌段共聚物中,聚合物嵌段A1和聚合物嵌段A2的结构可以相同也可以不同。 As the polymer block A2, the same block as that of the above-mentioned polymer block A1 can be used. The description of the polymer block A1 can be appropriately applied to the points that are not particularly described for the polymer block A2. In the A1-B-A2 type tri-block copolymer, the structures of the polymer block A1 and the polymer block A2 may be the same or different. the
特别地,聚合物嵌段A1及A2优选均为苯乙烯。即,弹性长丝13优选下述构成:仅含有聚苯乙烯作为聚合物嵌段A1,且仅含有聚苯乙烯作为聚合物嵌段A2。
In particular, polymer blocks A1 and A2 are preferably both styrene. That is, the
A1-B-A2型三嵌段共聚物中聚合物嵌段A1及A2的总含量相对于A1-B-A2型三嵌段共聚物的整个结构单元,优选为15~40重量%、更优选为18~30重量%。 The total content of the polymer blocks A1 and A2 in the A1-B-A2 type triblock copolymer is preferably 15 to 40% by weight, more preferably, relative to the entire structural unit of the A1-B-A2 type triblock copolymer It is 18 to 30% by weight. the
另外,如上所述,当聚合物嵌段A1及A2均为聚苯乙烯时,A1-B-A2型三嵌段共聚物中聚合物嵌段A1和聚合物嵌段A2的比例以重量比计优选为(A1/A2)=0.8~1.2、更优选为(A1/A2)=0.9~1.1。 In addition, as mentioned above, when the polymer blocks A1 and A2 are both polystyrene, the ratio of the polymer block A1 and the polymer block A2 in the A1-B-A2 type triblock copolymer is calculated by weight ratio Preferably it is (A1/A2)=0.8-1.2, More preferably, it is (A1/A2)=0.9-1.1. the
聚合物嵌段B以聚烯烃为主体而构成。作为构成该聚烯烃的烯烃,可列举出例如异戊二烯、丁二烯、乙烯、丙烯、丁烯等。构成聚合物嵌段B的烯烃可以由这些烯烃中的1种构成,也可以由2种以上构成。在这些烯烃中,从耐候性、伸缩特性的观点出发,优选乙烯、丙烯。 The polymer block B is mainly composed of polyolefin. Examples of the olefin constituting the polyolefin include isoprene, butadiene, ethylene, propylene, butene and the like. The olefin constituting the polymer block B may consist of one type of these olefins, or may consist of two or more types. Among these olefins, ethylene and propylene are preferable from the viewpoint of weather resistance and stretchability. the
聚合物嵌段B中上述聚烯烃的含量相对于聚合物嵌段B的整个结构单元,优选为90~100重量%、更优选为95~100重量%。 The content of the polyolefin in the polymer block B is preferably 90 to 100% by weight, more preferably 95 to 100% by weight, based on the entire structural unit of the polymer block B. the
聚合物嵌段B除了上述聚烯烃以外,还可以含有由其它的聚合性单体衍 生的可以与聚烯烃聚合的其它聚合物而构成。作为该其它的聚合性单体,可列举出例如苯乙烯。构成聚合物嵌段B的上述可以与聚烯烃聚合的其它聚合物可以由这些其它的聚合性单体中的1种构成,也可以由2种以上构成。 The polymer block B may contain other polymers derived from other polymerizable monomers that can be polymerized with polyolefins in addition to the above-mentioned polyolefins. As this other polymerizable monomer, styrene is mentioned, for example. The above-mentioned other polymers that can be polymerized with polyolefins that constitute the polymer block B may be composed of one type of these other polymerizable monomers, or may be composed of two or more types. the
聚合物嵌段B中上述其它的聚合物的含量相对于聚合物嵌段B的整个结构单元,优选为0~10重量%、更优选为0~5重量%。 The content of the above-mentioned other polymers in the polymer block B is preferably 0 to 10% by weight, more preferably 0 to 5% by weight, based on the entire structural unit of the polymer block B. the
作为聚合物嵌段B的具体例子,可列举出聚异戊二烯、聚丁二烯、聚(乙烯-丙烯)、聚(乙烯-丁烯)等。其中,聚(乙烯-丙烯)由于耐候性、伸缩特性的缘故而优选。 Specific examples of the polymer block B include polyisoprene, polybutadiene, poly(ethylene-propylene), poly(ethylene-butylene), and the like. Among them, poly(ethylene-propylene) is preferable in terms of weather resistance and stretchability. the
A1-B-A2型三嵌段共聚物中聚合物嵌段B的含量相对于A1-B-A2型三嵌段共聚物的整个结构单元,优选为60~85重量%、更优选为70~82重量%。 The content of the polymer block B in the A1-B-A2 type triblock copolymer is preferably 60 to 85% by weight, more preferably 70 to 70% by weight relative to the entire structural unit of the A1-B-A2 type triblock copolymer. 82% by weight. the
作为优选的A1-B-A2型三嵌段共聚物的具体例子,可列举出苯乙烯-丁二烯-苯乙烯嵌段共聚物(SBS)、苯乙烯-异戊二烯-苯乙烯嵌段共聚物(SIS)、作为SBS的氢化物的苯乙烯-乙烯-丁烯-苯乙烯嵌段共聚物(SEBS)、作为SIS的氢化物的苯乙烯-乙烯-丙烯-苯乙烯嵌段共聚物(SEPS)、苯乙烯-乙烯-乙烯-丙烯-苯乙烯嵌段共聚物(SEEPS)等。其中,SEBS、SEPS、SEEPS由于可以获得热稳定性和耐候性优异的弹性长丝13而优选。
Specific examples of preferred A1-B-A2 type triblock copolymers include styrene-butadiene-styrene block copolymer (SBS), styrene-isoprene-styrene block Copolymer (SIS), Styrene-ethylene-butylene-styrene block copolymer (SEBS) as a hydrogenated product of SBS, Styrene-ethylene-propylene-styrene block copolymer ( SEPS), styrene-ethylene-ethylene-propylene-styrene block copolymer (SEEPS), etc. Among them, SEBS, SEPS, and SEEPS are preferable because
作为A1-B-A2型三嵌段共聚物,也可以使用市售品。作为在本发明中优选使用的A1-B-A2型三嵌段共聚物的市售品,可列举出例如Kraton Polymers公司的商品名“Kraton”、旭化成化学株式会社的商品名“Tuftec”及“TUFPRENE”、株式会社Kuraray的商品名“SEPTON”、“Hybrar”系列等。 Commercially available items can also be used as the A1-B-A2 type triblock copolymer. As a commercially available product of the A1-B-A2 type triblock copolymer preferably used in the present invention, for example, the trade name "Kraton" of Kraton Polymers, the trade name "Tuftec" and "Tuftec" of Asahi Kasei Chemical Co., Ltd. TUFPRENE", Kuraray's trade name "SEPTON", "Hybrar" series, etc. the
A1-B-A2型三嵌段共聚物可以通过例如下述工序来合成。首先,在环己烷等烃溶剂中添加乙烯基芳香族化合物,以有机锂化合物或金属钠等为引发剂进行阴离子聚合,得到聚合物嵌段A1。然后,添加烯烃单体进行聚合,得到聚合物嵌段A1-B。烯烃单体为共轭二烯时,对该共聚物的基于共轭二烯的双键加氢,得到目标聚合物嵌段A1-B。从耐热性、耐候性的观点出发,基于共轭二烯的双键的氢化率优选为共轭二烯的双键的80%以上、特别优选为90%以上。氢化反应可以使用铂、钯等贵金属系催化剂、有机镍化合物、有机钴化合物或这些化合物与其它有机金属化合物的复合催化剂来进行。氢化率可以利用碘值测定法算出。然后,添加乙烯基芳香族化合物进行聚合,从而得到聚合物嵌段A1-B-A2。 The A1-B-A2 type triblock copolymer can be synthesized by, for example, the following procedure. First, a vinyl aromatic compound is added to a hydrocarbon solvent such as cyclohexane, and anionic polymerization is performed using an organic lithium compound or metal sodium as an initiator to obtain a polymer block A1. Then, an olefin monomer was added and polymerized to obtain a polymer block A1-B. When the olefin monomer is a conjugated diene, the double bond based on the conjugated diene of the copolymer is hydrogenated to obtain the target polymer block A1-B. From the viewpoint of heat resistance and weather resistance, the hydrogenation rate based on the double bond of the conjugated diene is preferably 80% or more of the double bond of the conjugated diene, particularly preferably 90% or more. The hydrogenation reaction can be carried out using noble metal catalysts such as platinum and palladium, organic nickel compounds, organic cobalt compounds, or composite catalysts of these compounds and other organic metal compounds. The hydrogenation rate can be calculated by the iodine value measurement method. Then, a vinyl aromatic compound is added and polymerized to obtain polymer blocks A1-B-A2. the
构成弹性长丝13的上述树脂组合物可以仅含有上述A1-B-A2型三嵌段共聚物而构成,也可以根据需要,在不损害本发明目的的范围内,在除了A1-B-A2型三嵌段共聚物以外,还含有其它的1种或2种以上的树脂而构成。当上述树脂组合物含有A1-B-A2型三嵌段共聚物和其它树脂时,该树脂组合物中A1-B-A2型三嵌段共聚物的含量优选为90~100重量%、更优选为95~100重量%。但是,从纺丝成形性及伸缩性最大限度地提高的观点出发,上述树脂组合物优选仅含有A1-B-A2型三嵌段共聚物而构成。
The above-mentioned resin composition constituting the
另外,上述树脂组合物可以含有1种A1-B-A2型三嵌段共聚物而构成,也可以含有结构不同的2种以上的A1-B-A2型三嵌段共聚物而构成。 In addition, the aforementioned resin composition may contain one type of A1-B-A2 type triblock copolymer, or may contain two or more types of A1-B-A2 type triblock copolymers having different structures. the
当上述树脂组合物除了A1-B-A2型三嵌段共聚物以外还含有其它树脂时,作为所述的其它树脂,可以使用例如橡胶、或聚烯烃系弹性体、聚酯系弹性体、聚氨酯系弹性体等热塑性弹性体等。另外,可以使用热塑性弹性体以外的树脂、例如聚乙烯、聚丙烯等热塑性树脂等。它们也可以组合2种以上来使用。 When the above-mentioned resin composition contains other resins besides the A1-B-A2 type triblock copolymer, as the other resins, for example, rubber, or polyolefin-based elastomers, polyester-based elastomers, polyurethanes, etc., can be used. Thermoplastic elastomers such as elastomers, etc. In addition, resins other than thermoplastic elastomers, for example, thermoplastic resins such as polyethylene and polypropylene, and the like can be used. These can also be used in combination of 2 or more types. the
上述树脂组合物可以通过将A1-B-A2型三嵌段共聚物、或A1-B-A2型三嵌段共聚物及上述其它树脂用各种公知的方法进行熔融混合来获得。例如,将上述各成分同时地或依次地装入亨舍尔混合机、V型混合机、转鼓混合机、带式混合机等中进行混合后,用单螺杆挤出机、多螺杆挤出机、捏合机、密闭式混炼机等混炼装置进行熔融混炼,从而获得上述树脂组合物。 The above-mentioned resin composition can be obtained by melt-mixing the A1-B-A2 type triblock copolymer, or the A1-B-A2 type triblock copolymer and the above-mentioned other resins by various known methods. For example, the above-mentioned components are simultaneously or sequentially loaded into a Henschel mixer, a V-type mixer, a drum mixer, a ribbon mixer, etc. for mixing, and then extruded with a single-screw extruder or a multi-screw extruder. kneading machine, kneader, internal kneader and other kneading equipment to obtain the above-mentioned resin composition. the
上述树脂组合物中除了上述树脂成分(A1-B-A2型三嵌段共聚物、其它树脂)以外,还可以根据需要,在不损害本发明目的的范围内含有增塑剂(例如石蜡系油、石蜡系蜡、环烷烃系油、乙烯-α-烯烃寡聚物、低分子量聚乙烯等)、耐候稳定剂、耐热稳定剂、防静电剂、润滑剂、增滑剂、成核剂、阻燃剂、颜料、染料、无机或有机填充剂等。 In addition to the above-mentioned resin components (A1-B-A2 type triblock copolymer, other resins), the above-mentioned resin composition may also contain a plasticizer (such as a paraffinic oil , paraffin wax, naphthene oil, ethylene-α-olefin oligomer, low molecular weight polyethylene, etc.), weathering stabilizer, heat stabilizer, antistatic agent, lubricant, slip agent, nucleating agent, Flame retardants, pigments, dyes, inorganic or organic fillers, etc. the
上述树脂组合物在以245℃的温度加热熔融的状态下,从内径为0.45mm、长度为4.5mm的圆筒形状的喷嘴中以8.4m/分钟的喷出速度喷出时,熔融张力的最大值优选为0.06~0.20cN、更优选为0.07~0.15cN。图4中示出了熔融张力的测定方法。测定对图4所示的负荷传感器施加的向上的力,将该测定值作为熔融张力。通过使构成弹性长丝13的树脂组合物的熔融张力的最大值在上述范围内,可以使纺丝成形性变得更好。熔融张力的调整可以通过添加例 如增塑剂(石蜡等)、橡胶、热塑性树脂等来进行。如上所述构成的树脂组合物的熔融张力在上述范围内。
When the above-mentioned resin composition is heated and melted at a temperature of 245°C, when it is ejected from a cylindrical nozzle with an inner diameter of 0.45mm and a length of 4.5mm at a discharge speed of 8.4m/min, the maximum melt tension is The value is preferably 0.06 to 0.20 cN, more preferably 0.07 to 0.15 cN. Fig. 4 shows the method of measuring the melt tension. The upward force applied to the load cell shown in FIG. 4 was measured, and the measured value was regarded as the melt tension. When the maximum value of the melt tension of the resin composition constituting the
配置在2张无纺布11、12之间的、由大量弹性长丝13构成的弹性长丝的表观单位面积重量从伸缩特性、手感、厚度、成本的观点出发,优选为4~30g/m2、特别优选为6~15g/m2。
The apparent basis weight of the elastic filaments composed of a large number of
下面,参照着图5对本实施方式的伸缩片材10的优选制造方法进行说明。在本制造方法中,将从纺丝喷嘴16中纺出的熔融状态的大量弹性长丝13以规定速度牵拉并进行拉伸,并且在该弹性长丝13固化之前,按照该该弹性长丝13相互不交叉地沿一个方向排列的方式使该弹性长丝与无纺布11、12熔融粘合,然后将熔融粘合有该弹性长丝13的复合体19沿着该弹性长丝13的延伸方向进行弹性表现处理,从而使该无纺布复合体19具有伸缩性。
Next, a preferable manufacturing method of the
纺丝喷嘴16设置在纺丝头17上。纺丝头17与挤出机连接。也可以通过齿轮泵向纺丝头17供给树脂。利用该挤出机熔融混炼的弹性树脂被供给至纺丝头17。在纺丝头17上,大量的纺丝喷嘴16以直线状配置成一列。纺丝喷嘴16沿着第1及第2无纺布11、12的宽度方向配置。相邻的纺丝喷嘴16的间隔相当于目标伸缩片材10中弹性长丝13的间隔。纺丝喷嘴16通常为圆形,其直径(内径)会影响到弹性长丝13的直径及拉伸倍率。从该观点出发,纺丝喷嘴16的直径(内径)优选为0.1~2mm、特别优选为0.2~0.6mm。为了提高与无纺布11、12的接合强度、提高弹性长丝13的纺丝性、以及提高伸缩片材10的伸缩特性,也可以将弹性长丝13制成复合形态(并列型、芯鞘、海岛结构)。具体来说,优选PP系的弹性体树脂和苯乙烯系的弹性体树脂的组合。
The spinning
纺出的熔融状态的弹性长丝13分别与从坯料卷以彼此相同的速度纺出的第1无纺布11及第2无纺布12合流,然后夹持在两无纺布11、12之间并以规定速度进行牵拉。弹性长丝13的牵拉速度与两无纺布11、12的纺出速度一致。弹性长丝13的牵拉速度会影响到该弹性长丝13的直径及拉伸倍率。通过拉伸对弹性长丝13产生的张力会防止在将该弹性长丝13与无纺布11、12贴合时由风或静电引起的该弹性长丝13的飘散。由此,可以使各弹性长丝彼此不交叉地沿一个方向排列。从这些观点出发,弹性长丝13的牵拉速度优选调整为相对于纺丝喷嘴孔内的树脂喷出速度,其拉伸倍率为1.1~400倍、 特别为4~100倍、进一步为10~80倍。
The
弹性长丝13在其固化前、即在可熔融粘合的状态下与第1及第2无纺布11、12合流。结果,弹性长丝13以夹持在第1及第2无纺布11、12间的状态与上述无纺布11、12熔融粘合。即,在使固化前的弹性长丝与搬送的无纺布11、12熔融粘合的同时,将弹性长丝13牵拉并进行拉伸。在弹性长丝13熔融粘合时,对第1及第2无纺布11、12并不从外部施加热。即,仅通过可熔融粘合的弹性长丝13所产生的熔融热来将该弹性长丝13与两无纺布11、12熔融粘合。结果,仅两无纺布11、12的构成纤维中存在于弹性长丝13周围的纤维与该弹性长丝熔融粘合,而存在于远离该位置的纤维不发生熔融粘合。结果,将对两无纺布11、12施加的热控制在最小限,因此可以维持该无纺布自身本来具有的良好的手感。由此,所得伸缩片材10的手感变得良好。
The
从纺丝喷嘴16中纺出的熔融状态的弹性长丝13与无纺布11、12接触前,该弹性长丝13从该纺丝喷嘴16的顶端16a起算的移动距离L(纺丝喷嘴顶端16a和熔融状态的弹性长丝13与无纺布11、12在最初接触时其接触部11a、12a之间的最短距离,参见图6)优选为600mm以下、特别优选为100~500mm。通过使熔融状态的弹性长丝13的移动距离L为600mm以下,可以在熔融状态的弹性长丝固化前使该弹性长丝与无纺布可靠地熔融粘合,从而可以更可靠地得到层间接合强度与伸缩特性之间平衡性优异的伸缩片材,即伸缩片材中弹性长丝与无纺布之间的接合强度为10cN/25mm以上,且伸缩片材中的弹性树脂的每单位面积重量的25%回复强度为1.0cN/{50mm·(g/m2)}以上。另外,通过使熔融状态的弹性长丝13的移动距离L为100mm以上,通过将熔融了的弹性长丝13冷却而提高弹性树脂的粘度,从而使弹性长丝13在夹持辊18a、18b之间难以被压坏。由此,可以使弹性长丝13与构成可伸长的无纺布11、12的纤维之间的平均接合比例在前述优选的范围内。另一方面,通过使熔融状态的弹性长丝13的移动距离L为600mm以下,长丝不会因静电或风等而飘散,长丝之间的粘接、重叠或长丝断裂等的发生频率变低,因此优选将该移动距离L的上限设为600mm。
Before the
移动距离L的调整可以通过纺丝喷嘴和/或夹持辊的位置的调整来进行。在本实施方式中,弹性长丝13与无纺布11、12的熔融粘合如下进行:将从纺丝喷嘴16中纺出的熔融状态的所述弹性长丝13和搬送中的所述无纺布11、 12在一对夹持辊18a、18b之间合流并通过。在本实施方式的伸缩片材10中,如上所述,弹性长丝13在其整个长度上与无纺布11、12接合,在本制造方法中,为了实现这样的接合形态,作为一对的夹持辊18a、18b,分别使用在辊圆周面上没有凹凸的圆筒形状的辊。
The adjustment of the moving distance L can be performed by adjusting the position of the spinning nozzle and/or the nip roll. In this embodiment, the fusion bonding of the
在纺出的弹性长丝13与第1及第2无纺布11、12合流前的过程中,该弹性长丝13被拉伸,并且分子在拉伸方向上取向。而且直径变小。通过分子取向,可以得到50%伸长时强度的伸长/回复比小的弹性长丝13。从充分拉伸弹性长丝13的观点和防止弹性长丝13的断丝的观点出发,也可以对纺出的弹性长丝13吹附规定温度的风(热风、冷风)以调整该弹性长丝13的温度。
Before the spun
弹性长丝13的拉伸并不仅是原料树脂在熔融状态下的拉伸(熔融拉伸),也可以是在其冷却过程中的软化状态下的拉伸(软化拉伸)。熔融状态是指施加外力时树脂能够流动的状态。树脂的熔融温度通过粘弹性测定(例如对夹在圆形并行平板间的树脂施加旋转方向的振动形变来进行测定)、以Tanδ的峰温度的形式来测定。为了在弹性树脂拉伸时不发生断丝,较长地确保拉伸区间即可。从该观点出发,弹性树脂的熔融温度优选为130~300℃。另外,从弹性树脂的耐热性的观点出发,熔融温度优选为220℃以下。为了提高树脂的流动性以优化成形性,弹性长丝13的成形温度(塑模的温度)优选为原料树脂的熔融温度的+50℃以上,由于耐热性,上述成形温度优选为原料树脂的熔融温度的+110℃以下。软化温度以制成片材状的弹性树脂的测定试样的粘弹性特性中的Tg温度的形式来测定。从软化温度到熔融温度的范围称为软化状态。另外,将比软化温度低的温度的状态称为固化状态。从伸缩片材10的保存时弹性树脂的晶体成长、体温导致的伸缩片材10的伸缩特性降低的观点出发,软化温度优选为60℃以上、更优选为80℃~180℃。
The stretching of the
为了可靠地进行纤维熔融粘合,弹性长丝13与无纺布11、12接合时弹性长丝13的温度优选为100℃以上,更优选为120℃以上,进一步优选为140℃以上。另外,从保持弹性长丝13的形状以获得伸缩特性良好的伸缩片材10的观点出发,弹性长丝的温度优选为180℃以下。更优选为160℃以下的范围。其综合结果是:最合适的长丝温度为120~160℃、更优选为140~160℃的范围。接合时的温度使用由具有与构成弹性长丝的弹性树脂的熔点不同的熔点的改性聚乙烯或改性聚丙烯等构成的薄膜作为与弹性长丝13接合的层叠基 材,并观察其接合状态来进行测定。此时,如果弹性长丝与层叠基材发生熔融粘合,则接合温度为层叠基材的熔点以上。
The temperature of the
弹性长丝13与无纺布11、12接合时,弹性长丝13实质上为未伸长状态(除去外力时不收缩的状态)。在两者的接合状态下,构成无纺布11、12的纤维的至少一部分优选与弹性长丝熔融粘合,或者更优选与弹性长丝13和构成无纺布11、12的纤维的至少一部分这二者都发生熔融粘合。因为这样可以获得充分的接合强度。所得伸缩片材10的伸缩特性会受到弹性长丝13与无纺布11、12的接合点的密度的影响。另外,伸缩特性可以通过接合温度、接合压力、后述的无纺布11、12的弹性表现处理带来的接合点的错开来进行调整。通过使无纺布11、12的构成纤维与弹性长丝13熔融粘合,一个个接合点的接合强度提高。如果降低接合点的密度,则无纺布11、12带来的伸缩阻碍降低,且可以获得具有充分接合强度的伸缩片材10,因此是优选的。
When the
在使弹性长丝13与第1及第2无纺布11、12合流时,各弹性长丝13相互不交叉地沿一个方向排列。然后,在使弹性长丝13与第1及第2无纺布11、12合流并在两无纺布11、12间夹持该弹性长丝13的状态下,用一对夹持辊18、18对这三者进行夹压。夹压的条件会对所得伸缩片材10的手感产生影响。如果夹压力过大,则弹性长丝13容易陷入两无纺布11、12内,由此容易使所得伸缩片材10的手感降低。从该观点出发,夹持辊18、18产生的夹压力只要是使弹性长丝13与两无纺布11、12接触的程度就足够了,没有必要施加过高的夹压力。
When the
在使上述弹性长丝13与第1及第2无纺布11、12合流并在两无纺布11、12间夹持该弹性长丝13的状态下,用一对捏合辊18、18对这三者进行夹压的其它的优选方法有:弹性长丝13和无纺布11、12合流、在上述一对夹持辊18a、18b间设置间隔W的方法(参照图6)。与上述同样,从对弹性长丝不带来损伤且获得充分的接合强度的观点出发,在18a、18b间设置的间隔W优选为0.05~1mm、特别优选为0.05~0.5mm。
In the state where the
将接合前的无纺布11、12各自的厚度、及弹性长丝13即将接合(夹持)前的厚度(沿无纺布的厚度方向的厚度)的合计值设为T0时,上述一对夹持辊18a、18b间的间隔W与T0之比W/T0优选为0.05~0.8、特别优选为0.1~0.4。无纺布的厚度可以通过前述的方法求得。弹性长丝的厚度(mm)以 (G/ρvnπ)求得。其中,G为整个机械宽度上的每单位时间的挤出量(g/min)、n为整个机械宽度上的长丝根数、v为夹持辊速度(m/min)、ρ为长丝树脂的密度(g/cm3)。通过使W/T0在上述范围内,弹性长丝与无纺布构成纤维的接合点密度和无纺布构成纤维在弹性长丝中的陷入之间获得平衡,由此可以兼顾上述的弹性长丝与无纺布之间的接合强度和单位伸缩片材的构成树脂单位面积重量的25%回复强度。
When the total value of the thickness of each of the
作为利用夹持辊18进行的夹压的其它条件,可列举出夹持辊18的温度。本发明人等的研究结果是:与其在加热夹持辊18的状态下进行夹压,还不如不进行加热(即听其自然)、或边冷却边进行夹压,能够获得手感良好的伸缩片材10。在冷却夹持辊18时,优选使用冷却水等冷却介质,将夹持辊18的表面设定温度调节为10~50℃。
The temperature of the
如此获得在2张无纺布11、12间夹持有弹性长丝13的复合体19。在使用原本具有伸长性的无纺布作为无纺布11、12时,该复合体19为伸缩片材10本身。另一方面,在使用原本不具有伸长性的无纺布作为无纺布11、12时,将包含该无纺布11、12的复合体19沿着弹性长丝13的延伸方向进行弹性表现处理,从而进行使该复合体19具有伸缩性的操作。在本制造方法中,该操作如下进行:使用具备分别在圆周方向上交替形成有齿和齿沟的一对齿槽辊20、21的弹性表现处理装置22,将复合体19沿着其搬送方向、即沿着弹性长丝13的延伸方向进行弹性表现处理。
In this way, a composite 19 in which the
弹性表现处理装置22具有使一个或两个齿槽辊20、21的枢支部上下变位的公知的升降机构(未图示),因此齿槽辊20、21间的间隔能够调节。在本制造方法中,各齿槽辊20、21的组合方式是一个齿槽辊20的齿插在另一个齿槽辊21的齿间,而另一个齿槽辊21的齿插在一个齿槽辊20的齿间,将复合体19插入到该状态的两齿槽辊20、21间,然后对其进行弹性表现处理。
The elastic
在弹性表现处理装置22中,一对齿槽辊20、21二者可以通过驱动源来驱动(共转辊),也可以仅一方的齿槽辊20或21通过驱动源来驱动(随转辊),在本制造方法中,仅下侧的齿槽辊21通过驱动源驱动,上侧的齿槽辊20并没有与驱动源连接,而是随着齿槽辊21的旋转随动(随转)。随转辊的使用容易使弹性表现处理加工后的伸缩片材10上清楚地出现高单位面积重量部分14及低单位面积重量部分15的条纹花样,从提高伸缩片材10的图案设计性、 和使单位面积重量比低单位面积重量部15低以提高透气性的观点出发,随转辊的使用是优选的。作为齿槽辊20、21的齿形,优选使用一般的渐开齿形、摆线齿形,特别优选使用将这些齿的宽度变窄的齿形。
In the elastic
图7中示意地示出了复合体19弹性表现处理的状态。在复合体19通过齿槽辊20、21间时,复合体19在与齿槽辊20、21的齿23、24接触的区域(P3-P2间、P1-P4间)基本不被拉伸。与此相对,通过作为驱动辊的齿槽辊21的齿24的齿面,在向着作为随动辊的齿槽辊20的齿23的齿面被挤压的区域(P2-P1间),通过两齿20、21被大大地拉伸。另外,通过齿槽辊21的齿24的顶端部,在从齿槽辊20的齿23拉离的区域(P4-P3间),虽然达不到上述区域(P2-P1间)的程度,但也被大大地拉伸。
FIG. 7 schematically shows the state of the elastic expression treatment of the
另外,复合体19在与齿槽辊20、21的齿23、24的顶端部接触的区域(P3-P2间、P1-P4间),如上所述,基本不被拉伸,但通过齿23、24的顶端部,在其直径方向上、即在复合体19的厚度方向上被局部地挤压,因此在厚度方向上变薄。但是,由于区域(P3-P2间)和区域(P1-P4间)间被局部地挤压的方向朝向相反的方向,因此变薄的方向也朝向相反方向。
In addition, the
通过上述拉伸工艺,可以防止弹性长丝13与两无纺布11、12之间的剥离,而且可以有效地拉伸复合体19中的两无纺布11、12,从而可以使复合体19具有伸缩性。另外,大大被拉伸的区域(P2-P1间及P4-P3间)成为低单位面积重量部分15,基本不被拉伸的区域(P3-P2间、P1-P4间)成为高单位面积重量部分14。
Through the above stretching process, the
特别是,在无纺布11、12中含有低拉伸的纤维时,在上述(P2-P1)间及(P4-P3)间,该纤维被拉伸而变细,从而形成纤维粗细度发生周期性变化的不定径纤维。
In particular, when the
齿槽辊20、21产生的拉伸力主要作用于低拉伸纤维的拉伸,对无纺布11、12与弹性长丝13之间的接合部位不会施加过度的力。其结果,可以防止该接合部位的破坏,防止发生无纺布11、12与弹性长丝13剥离,而且可以有效地拉伸复合体19。另外,通过该拉伸,如图8所示,在不破坏纤维间的接合的情况下,无纺布11、12充分地伸长,由此,无纺布11、12阻碍弹性长丝13自由伸缩的程度大大降低。其结果,根据本制造方法,可以有效地制造高强度、高伸缩性、且破损和起毛少的外观良好的伸缩片材10。另外,在图8 中,为了方便,将通过拉伸产生的非弹性纤维的粗细度表示成一样的。
The stretching force generated by the
如上所述,在无纺布11、12中含有低拉伸的纤维时,由于可以将该纤维顺利地进行弹性表现处理,且这些纤维间的接合不会被拉伸所破坏,因此弹性表现处理带来的无纺布11、12的强度降低可以尽量地得到控制。具体来说,拉伸后得到的伸缩片材10的拉伸强度与弹性表现处理前的复合体19的拉伸强度之比为0.3~0.99、特别地为0.5~0.99、进一步为0.7~0.99这样的接近1的值。这里所说的拉伸强度可以按照下述的最大强度的测定方法来测定。
As mentioned above, when the
<最大强度的测定> <Determination of maximum strength>
将伸缩片材10按其伸缩方向上为200mm、与该伸缩方向垂直的方向上为50mm的大小切出矩形的试验片。将夹头间距离设定为150mm。使试验片向伸缩片材10的伸缩方向以300mm/分钟的速度伸长,测定此时的负荷。将此时的最大点的负荷作为最大强度。通过同样的方法,也对弹性表现处理前的复合体19测定最大强度。在测定环境温度为22℃、湿度为65%RH的条件下、优选使用岛津制作所制的牵拉试验机AG-1kNIS来测定上述最大强度。
The
复合体19通过一对齿槽辊20、21来进行弹性表现处理,由此获得目标伸缩片材10。所得伸缩片材10在通过齿槽辊20、21后,由于自身的收缩恢复力,在MD方向上的拉伸状态迅速被释放。其结果,伸缩片材10在搬送方向上的长度大致恢复。由此,在伸长了的状态下,高单位面积重量部分14及低单位面积重量部分15沿弹性长丝13的延伸方向交替地排列。另外,释放拉伸状态时,可以完全地释放拉伸状态,也可以在表现出伸缩性的限度内,在维持某种程度的拉伸状态的状态下释放拉伸状态。
The composite 19 is subjected to an elastic expressing process by a pair of
通过上述弹性表现处理加工,伸缩片材10的厚度相对于弹性表现处理加工前的复合体19的厚度,优选增加到1.1倍~4倍、特别优选增加到1.3倍~3倍。由此,通过两无纺布11、12的构成纤维发生塑性变性并伸长,从而纤维变细。与此同时,两无纺布11、12变得更加膨松,肌肤触感好,且弹性(缓冲性)变得良好。
The thickness of the
从表现出充分的伸缩特性的观点出发,如此得到的伸缩片材10沿弹性长丝13的延伸方向伸长100%、并从该状态回复至50%时的负荷A(以下也称为50%回复强度)、与沿弹性长丝13的延伸方向伸长50%时的负荷B(以下也称为50%伸长强度)之比(A/B)优选为50%以上、特别优选为65%以上。
From the viewpoint of exhibiting sufficient stretch properties, the load A (hereinafter also referred to as 50%) when the thus obtained
另外,虽然根据具体用途的不同而不同,但伸缩片材10的整体的单位面积重量优选为10~150g/m2、特别优选为25~60g/m2。关于伸缩片材10的厚度,优选为0.05~5mm、特别优选为0.5~2mm。伸缩片材10的厚度可以通过与前述的各无纺布11、12的厚度的测定同样的方法来进行测定。
In addition, although it varies depending on specific uses, the entire basis weight of the
本实施方式的伸缩片材10优选用作短裤型一次性尿布的外包装材料。此时,也可以将本实施方式的伸缩片材10作为置于外侧的片材,使用非伸缩性片材作为置于内侧的片材,将两片材贴合后作为上述外包装材料使用。另外,除了该用途以外,也可以利用其良好的手感、防起毛性、伸缩性、透气性等优点,用作医疗用一次性衣服、清扫片材、眼罩、面膜、绷带等各种的用途中。特别优选用作生理用卫生巾或一次性尿布等吸收性物品的构成材料。作为该构成材料,可列举出例如比吸収体更靠肌肤侧的液体透过性的片材(包括正面片材、亚层等)、构成一次性尿布的外表面的片材、用于使腰身部或腰部、腿周部等具有弹性伸缩性的片材等。另外,可以用作形成卫生巾的翼的片材等。另外,也可以用于虽然是这些以外的部位、但希望具有伸缩性的部位等中。伸缩片材10的单位面积重量或厚度可以根据其具体用途适当地调整。例如在作为吸收性物品的构成材料使用时,单位面积重量优选为20~60g/m2左右、厚度优选为0.5~1.5mm左右。
The
以上基于优选的实施方式对本发明进行了说明,但本发明并不限于上述实施方式。例如在上述实施方式的伸缩中是在2张无纺布11、12间夹持有大量的弹性长丝13的结构,但也可以取而代之,在1张无纺布表面上接合大量的弹性长丝来制成伸缩片材。此时,作为弹性长丝的构成材料,可以使用固化时粘附性低的树脂,这从在将伸缩片材10以卷成辊状的状态保存时防止阻滞的观点出发是优选的。
As mentioned above, although this invention was demonstrated based on preferable embodiment, this invention is not limited to the said embodiment. For example, in the expansion and contraction of the above-mentioned embodiment, a large number of
另外,上述实施方式中弹性长丝13都是相同的直径,并以等间距配置,因此对伸缩片材10的任何部分来说,伸长应力都是相同的。但是也可以取而代之,按照由在弹性长丝的伸长方向上伸长应力不同的2个以上的区域构成的方式来构成伸缩片材。2个以上的所述区域在所述伸长方向上大致并列地配置。此时,在伸长应力不同的各区域之间,相邻的弹性长丝的间距不同和/或弹性长丝的直径不同。由此,可以使各区域间的伸长应力不同。在制造伸缩片材时,也可以将2种以上不同的树脂导入任意的纺丝喷嘴中进行纺丝,从 而使各区域间的伸长应力不同。
In addition, in the above embodiment, the
也可以对伸缩片材10局部地进行压花加工,或者将弹性长丝13部分地切断或部分地热密封。这些操作是为了在伸缩片材10上形成不伸缩的部分、或局部地提高强度而进行的。或者,是为了与其它部件贴合、或使其具有设计性而进行的。
The
另外,关于将弹性长丝13与无纺布11、12接合后进行的弹性表现处理,拉伸方向不仅可以是无纺布11、12的移动方向,也可以例如是斜向的。而且,也可以组合2种以上的弹性表现处理方法,或者阶段性地提高拉伸倍率,或者部分地进行弹性表现处理。弹性表现处理方向不仅可以是一个方向,也可以是垂直的两个方向。也可以将沿一个方向伸缩的无纺布和沿与其垂直的方向伸缩的无纺布接合,从而使伸缩片材在全部方向上具有伸缩性。
In addition, the stretching direction may be not only the moving direction of the
另外,在上述实施方式的制造方法中,在复合体19的弹性表现处理加工中使用了具备一对齿槽辊20、21的弹性表现处理装置,但也可以取而代之,使用具备拉幅机的弹性表现处理装置来进行弹性表现处理加工。
In addition, in the manufacturing method of the above-mentioned embodiment, the elasticity expressing processing apparatus provided with a pair of tooth-groove rolls 20 and 21 is used for the elastic expressing processing of the
另外,在上述制造方法中,作为将弹性长丝13与无纺布11、12接合的其它方法,也可以在一个的无纺布上直接挤出弹性长丝13而不进行熔融拉伸。此时的拉伸倍率为1倍。另外,也可以在将弹性长丝13与无纺布11、12接合前,在无纺布或弹性长丝上辅助性地涂布粘接剂,然后在弹性长丝实质上未伸长的状态下贴合。此外,也可以不涂布粘接剂,而是在重叠弹性长丝13和无纺布11、12后进行辅助性的热处理(利用热风法的热风吹附、蒸汽喷射、热压花)、机械交织(针刺法、射流喷网法)等。此时,也可以在单面或两面上使用纤维网来代替无纺布。
In addition, in the above-mentioned production method, as another method of joining the
实施例 Example
以下,通过实施例进一步详细地说明本发明。但是,本发明的范围并不限于这些实施例。 Hereinafter, the present invention will be described in further detail through examples. However, the scope of the present invention is not limited to these Examples. the
[实施例1-1] [Example 1-1]
使用图5所示的装置制造了图1及图2所示结构的伸缩无纺布。作为第1及第2无纺布11、12,使用了单位面积重量为15g/m2的热风法无纺布。该无 纺布的构成纤维是直径为19μm、最大伸长率为180%、纤维长度为44mm的芯鞘型复合纤维(芯:PET;鞘:PE)。作为弹性长丝13的原料树脂,使用了由SEPS树脂(重均分子量为5万,MFR为60g/10分钟(230℃,2.16kg))(JIS K7210:1999)构成的弹性体。纺丝条件是:纺丝头17的温度为310℃,纺丝喷嘴16的直径为400μm、纺丝喷嘴16的间距为1mm。弹性长丝13的直径为120μm。长丝的表观单位面积重量(样品中的长丝重量/采样片材面积)为10g/m2、拉伸倍率为11倍。拉伸倍率用(喷嘴孔径/伸缩表现处理前纤维直径)2来定义。复合体19的弹性表现处理加工使用具备在轴长方向上交替形成有齿和齿沟的一对齿槽辊20、21的弹性表现处理装置22来进行。齿间及齿沟间的间距分别为2.0mm(啮合状态下的齿间的间距P为1.0mm)。调整上下齿槽辊的压入量,以拉伸倍率为3.0倍将复合体19在弹性长丝13的延伸方向上进行弹性表现处理。由此得到沿弹性长丝13的延伸方向伸缩的单位面积重量为40g/m2的伸缩片材10。所得伸缩片材10透过无纺布呈现弹性长丝13产生的条纹花样。另外还呈现高单位面积重量区域及低单位面积重量区域产生的条纹花样。通过这两种条纹花样,伸缩片材也呈现格子状的花样。另外,伸缩片材10中的弹性长丝13具有长轴在该片材10的平面方向的椭圆形的截面,且长轴/短轴之比为1.6。1.5倍伸长时的宽度为原宽度的96%,宽度减缩为4%。通过显微镜确认了伸缩片材10中无纺布11、12的构成纤维沿纤维的长度方向的粗细度不一样。该构成纤维的最大纤维直径为26.1μm、最小纤维直径为6.8μm、纤维直径比为3.8。另外,纤维直径的粗细度在该范围内周期性地变化。
Stretchable nonwoven fabrics having the structures shown in FIGS. 1 and 2 were manufactured using the apparatus shown in FIG. 5 . As the first and second
[实施例1-2] [Example 1-2]
将纺丝喷嘴16的间距设定为在纺丝头17的宽度方向上为1mm,从而形成第1喷嘴列。然后,从第1喷嘴列开始,在纺丝头17的移动方向上离开1mm的位置上以与第1喷嘴列相同的间距形成第2喷嘴列。第1喷嘴列和第2喷嘴列相互错开半个间距地配置。另外,将弹性长丝13的拉伸倍率改为25倍,使弹性长丝13的直径为80μm,除此以外,与实施例1-1同样操作,获得伸缩片材10。该伸缩片材10中,弹性长丝13的间距为0.5mm。
The pitch of the spinning
[实施例1-3] [Example 1-3]
形成第1区域,其中将纺丝喷嘴16的喷嘴直径设定为400μm,将弹性长丝13的拉伸倍率设定为11倍,将弹性长丝13的直径设定为120μm;和形成第2区域,其中将纺丝喷嘴16的喷嘴直径设定为300μm,将弹性长丝13的拉伸倍率设定为18倍,将弹性长丝13的直径设定为70μm。除此以外,与实施例1-1同样操作,获得伸缩片材10。第1区域及第2区域在伸缩片材10的宽度方向上并列。该伸缩片材中粗细度不同的2种弹性长丝的直径分别测定。
Forming the first region, wherein the nozzle diameter of the spinning
[实施例1-4] [Example 1-4]
在实施例1-1使用的苯乙烯系弹性体中干混1.5重量%的紫色的着色母料配混料(PE系树脂基质,颜料浓度为60重量%的产品),除了使用紫色的弹性长丝13以外,与实施例1-1同样操作,获得伸缩片材10。在该伸缩片材中,透过无纺布,弹性长丝13产生的条纹花样更加明显。
In the styrene-based elastomer used in Example 1-1, 1.5% by weight of purple coloring masterbatch compounding material (PE-based resin matrix, product with a pigment concentration of 60% by weight) was dry-blended, except that purple elastic long Except for the
[实施例1-5] [Example 1-5]
将实施例1-2中使用的复合体19在通过使用热风法的热风吹附进行了热处理后,在与实施例2同样的条件下进行拉伸加工,由此获得伸缩片材10。在该伸缩片材中,无纺布11、12各纤维彼此熔融粘合,接合强度进一步提高。
The composite 19 used in Example 1-2 was heat-treated by hot air blowing using the hot air method, and then stretched under the same conditions as in Example 2 to obtain a
[比较例1-1] [Comparative example 1-1]
按照专利文献1记载的方法制造伸缩片材。即,使用CONWED公司的伸缩纤维网(单位面积重量为73g/m2),作为第1及第2无纺布11、12,使用单位面积重量为20g/m2的热风法无纺布。该无纺布的构成纤维是直径为17μm、最大伸长率为30%、纤维长度为44mm的芯鞘型复合纤维(芯PET;鞘:PE)。相对于无纺布11、12的MD方向,伸缩纤维网的格子大致为正方形(MD方向、CD方向上均为3.2mm)。使用分别加热到约120℃和约60℃的金属压制机,对上述纤维网和无纺布以约10kg/cm2的压力进行10秒钟的热/压力结合。将所得片材使用具有在轴长方向上交替形成有大径部和小径部的一对凹凸辊(啮合状态下的齿间的间距P为1.0mm)的拉伸装置(弹性表现处理装置)进行弹性表现处理。由于无纺布的构成纤维不伸长,因此如果弹性表现处理的 拉伸倍率高,则会观察到无纺布上开孔的现象。因此,在使MD方向上的拉伸倍率为2.7倍的条件下进行处理。拉伸的程度通过调整上下的凹凸辊的压入量来进行控制。所得的伸缩片材由于难以伸长,因此宽度减缩变大。另外,感觉到弹性纤维网的硬梆梆的感觉,在手感方面较差。
A stretch sheet was produced according to the method described in Patent Document 1. That is, a stretchable fiber web (basis weight: 73 g/m 2 ) of CONWED was used, and as the first and second
[比较例1-2] [Comparative example 1-2]
与比较例1-1同样地使用CONWED公司的伸缩纤维网(单位面积重量为55g/m2)获得伸缩片材。相对于无纺布11、12的MD方向,伸缩纤维网的格子大致为菱形(MD方向、CD方向上均为9.5mm)。使用分别加热到约120℃和约60℃的金属压制机,对上述纤维网和无纺布以约10kg/cm2的压力进行10秒钟的热/压力结合。将所得片材使用具有在轴长方向上交替形成有大径部和小径部的一对凹凸辊(啮合状态下的齿间的间距P为1.0mm)的拉伸装置(弹性表现处理装置),在MD方向上进行3.0倍拉伸,进行弹性表现处理。在所得伸缩片材上,由于无纺布纤维不伸长,因此弹性表现处理时在无纺布上开了许多孔。因此,虽然片材整体有厚度,但弹性纤维网和无纺布的接合点较硬。结果在手感方面较差。
A stretchable sheet was obtained using a stretchable fiber web (weight per unit area: 55 g/m 2 ) of CONWED in the same manner as in Comparative Example 1-1. With respect to the MD direction of the
[评价] [evaluate]
对实施例及比较例中所得的伸缩片材,用以下的方法测定、评价50%回复强度/50%伸长强度、手感。另外,用上述方法测定伸缩片材和无纺布的厚度。将这些结果示于以下的表1中。 For the stretch sheets obtained in Examples and Comparative Examples, 50% recovery strength/50% elongation strength and hand feeling were measured and evaluated by the following methods. In addition, the thicknesses of the stretchable sheet and the nonwoven fabric were measured by the method described above. These results are shown in Table 1 below. the
[50%回复强度/50%伸长强度] [50% recovery strength/50% elongation strength]
将伸缩片材按照在其伸缩方向上为200mm、在与伸缩方向垂直的方向上为50mm的大小切出试验片。在岛津制作所制的牵拉试验机AG-1kNIS上按夹头间距离为150mm安装固定试验片。使试验片在其伸缩方向上以300mm/分钟的速度伸长。在伸长50%时记录负荷,将该值作为50%伸长强度。继续使该试验片伸长至100%,然后使其向回复方向(收缩方向)以相同速度收缩,形成伸长50%的状态。记录此时的负荷,作为50%回复强度。以上测定是在温度为20±2℃、湿度为65±5%RH的环境下进行的。 A test piece was cut out from the stretchable sheet to a size of 200 mm in the stretching direction and 50 mm in the direction perpendicular to the stretching direction. The test piece was installed and fixed on a tensile testing machine AG-1kNIS manufactured by Shimadzu Corporation so that the distance between chucks was 150 mm. The test piece was stretched at a rate of 300 mm/min in the stretching direction. The load was recorded at 50% elongation, and this value was taken as the 50% elongation strength. The test piece was further stretched to 100%, and then shrunk at the same speed in the recovery direction (shrinking direction) to form a 50% stretched state. Record the load at this time as 50% recovery strength. The above measurements are carried out in an environment with a temperature of 20±2° C. and a humidity of 65±5% RH. the
[手感] [feel]
让女性评价者10人在看不见伸缩片材的暗箱内、在温度为25℃、湿度为40%的环境下对该伸缩片材的手感进行评价。根据各评价者的评价,用下述分数进行打分,然后以评价者10人的平均分数(小数点以下四舍五入)作为手感的评价分数。 Ten female evaluators evaluated the texture of the stretchable sheet in an environment with a temperature of 25° C. and a humidity of 40% in a dark box where the stretchable sheet could not be seen. Based on the evaluation by each evaluator, the following points were used for scoring, and the average score (rounded up to one decimal point) of 10 evaluators was used as the evaluation score of texture. the
5分:手感好。 5 points: Feel good. the
4分:手感稍好。 4 points: Feeling is slightly better. the
3分:一般。 3 points: average. the
2分:手感稍差。 2 points: Feeling slightly poor. the
1分:手感差。 1 point: The hand feeling is bad. the
由表1所示的结果可知,各实施例的伸缩片材与比较例的伸缩片材相比,伸缩特性良好。另外可知有厚度且具有良好的手感。此外,在各实施例的伸缩片材中,弹性长丝相互基本不交叉、且相互不接触地分开配置。与此相对,比较例1-1的伸缩片材的弹性体由于压制而破坏,纤维网变得明显,且有纤维网的光泽,不能说外观良好。 From the results shown in Table 1, it can be seen that the stretchable sheets of the respective examples have better stretch properties than the stretchable sheets of the comparative examples. Moreover, it turns out that it has thickness and has favorable texture. In addition, in the stretch sheet of each example, the elastic filaments are arranged separately so that they do not substantially intersect each other and do not contact each other. On the other hand, the elastic body of the stretch sheet of Comparative Example 1-1 was destroyed by pressing, the fiber web became conspicuous, and the gloss of the fiber web was present, so it could not be said that the appearance was good. the
[实施例2-1~2-5及比较例2-1~2-3] [Example 2-1~2-5 and Comparative Example 2-1~2-3]
使用图5所示的装置获得复合体19(图1及图2所示伸缩片材10的前体),将其作为实施例2-1的样品。即,使用在单螺杆挤出机上安装有纺丝头17的结构的装置,上述纺丝头17具备纺丝喷嘴16,所述纺丝喷嘴16上以1mm的间隔在一条直线上排列有250个喷嘴孔,所述喷嘴孔是内径为0.45mm、长度为4.5mm的圆筒形状的孔,将作为树脂组合物的下述的三嵌段共聚物(1)~(8)以熔融温度为290℃、喷出量为0.3kg/分钟从纺丝喷嘴16中喷出,获得作为弹性长丝13的前体的长丝,将该长丝在从纺丝喷嘴16向下方离开100mm的位置处用热风法无纺布11、12夹住并使它们接合,从而获得弹性长丝13夹持在无纺布11和无纺布12之间的复合体19,其中所述热风法无纺布11、12是以150m/min的速度送出的单位面积重量为20g/m2、厚度为0.4mm、纤维直径为3dtex的无纺布。另外,无纺布11和12均是原本不具有伸长性的无纺布。
A composite 19 (precursor of the
在下述的8种A1-B-A2型三嵌段共聚物(1)~(8)中,三嵌段共聚物(1)~(5)是本发明范围内的化合物,三嵌段共聚物(6)~(8)是本发明的范围外的化合物。 In the following 8 kinds of A1-B-A2 type triblock copolymers (1)~(8), triblock copolymers (1)~(5) are compounds within the scope of the present invention, triblock copolymers (6) to (8) are compounds outside the scope of the present invention. the
[0195] A1-B-A2型三嵌段共聚物(1): A1-B-A2 type triblock copolymer ( 1 ):
将A1’-B’-A2’型三嵌段共聚物(SEPS三嵌段共聚物,苯乙烯含量为30重量%,乙烯-丙烯含量为70重量%,A1’、A2’的重均分子量为7500,B的重均分子量为35000)80重量%、和A1”-B”-A2”型三嵌段共聚物(SEPS三嵌段共聚物,苯乙烯含量为18重量%,乙烯-丙烯含量为82重量%,A1”、A2”的重均分子量为8100,B”的重均分子量为73800)20重量%用亨舍尔混合机混合,将所得聚合物作为三嵌段共聚物(1)使用。三嵌段共聚物(1)的上 述熔融张力的最大值(在以245℃的温度加热熔融的状态下,从内径为0.45mm、长度为4.5mm的圆筒形状的喷嘴孔中以8.4m/分钟的喷出速度喷出时的熔融张力的最大值)为0.07cN。 A1'-B'-A2' type triblock copolymer (SEPS triblock copolymer, styrene content is 30% by weight, ethylene-propylene content is 70% by weight, the weight average molecular weight of A1', A2' is 7500, the weight average molecular weight of B is 35000) 80% by weight, and A1 "-B"-A2 " type triblock copolymer (SEPS triblock copolymer, styrene content is 18% by weight, ethylene-propylene content is 82% by weight, the weight average molecular weight of A1", A2" is 8100, and the weight average molecular weight of B" is 73800) 20% by weight is mixed with a Henschel mixer, and the obtained polymer is used as a triblock copolymer (1) . The maximum value of the above-mentioned melt tension of the triblock copolymer (1) (in the state of heating and melting at a temperature of 245°C, measured at 8.4 m from a cylindrical nozzle hole with an inner diameter of 0.45 mm and a length of 4.5 mm The maximum value of the melt tension at the time of ejection at the ejection speed/minute) was 0.07 cN. the
三嵌段共聚物(1)中聚合物嵌段A1的重均分子量为:[(聚合物嵌段A1’的重均分子量)×(该A1’-B’-A2’在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)+(聚合物嵌段A1”的重均分子量)×(该A1”-B”-A2”在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)=]7620。 The weight-average molecular weight of the polymer block A1 in the triblock copolymer (1) is: [(the weight-average molecular weight of the polymer block A1') × (the A1'-B'-A2' contained in the resin composition The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers)+(the weight-average molecular weight of the polymer block A1″)×(the A1″-B″-A2 "The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers contained in the resin composition) =] 7620. the
三嵌段共聚物(1)中聚合物嵌段B的重均分子量为:[(聚合物嵌段B’的重均分子量)×(该A1’-B’-A2’在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)+(聚合物嵌段B”的重均分子量)×(该A1”-B”-A2”在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)=]42760。 The weight-average molecular weight of polymer block B in the three-block copolymer (1) is: [(the weight-average molecular weight of polymer block B') * (the A1 '-B'-A2 ' contained in the resin composition The percentage of the total amount of two or more A1-B-A2 type triblock copolymers)+(the weight-average molecular weight of the polymer block B ")×(the A1"-B"-A2 "The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers contained in the resin composition) =] 42760. the
三嵌段共聚物(1)中聚合物嵌段A2的重均分子量为:[(聚合物嵌段A2’的重均分子量)×(该A1’-B’-A2’在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)+(聚合物嵌段A2”的重均分子量)×(该A1”-B”-A2”在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)=]7620。 The weight-average molecular weight of the polymer block A2 in the triblock copolymer (1) is: [(the weight-average molecular weight of the polymer block A2') × (the A1'-B'-A2' contained in the resin composition The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers)+(the weight-average molecular weight of the polymer block A2")×(the A1"-B"-A2 "The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers contained in the resin composition) =] 7620. the
[0200] A1-B-A2型三嵌段共聚物(2): A1-B-A2 type triblock copolymer (2):
将A1-B-A2型三嵌段共聚物(SEPS三嵌段共聚物,苯乙烯含量为18重量%,乙烯-丙烯含量为82重量%,A1、A2的重均分子量为8100,B的重均分子量为73800)100重量%作为三嵌段共聚物(2)使用。三嵌段共聚物(2)的上述熔融张力的最大值为0.13cN。 A1-B-A2 type triblock copolymer (SEPS triblock copolymer, styrene content is 18% by weight, ethylene-propylene content is 82% by weight, the weight average molecular weight of A1, A2 is 8100, the weight of B The average molecular weight is 73800) and 100% by weight was used as the triblock copolymer (2). The above-mentioned maximum value of the melt tension of the triblock copolymer (2) was 0.13 cN. the
[0202] A1-B-A2型三嵌段共聚物(3): A1-B-A2 type triblock copolymer ( 3 ):
[0203] 将A1-B-A2型三嵌段共聚物(SEBS三嵌段共聚物、苯乙烯含量为20重量%,乙烯-丁烯含量为80重量%,A1、A2的重均分子量为9400,B的重均分子量为75200)100重量%作为三嵌段共聚物(3)使用。三嵌段共聚物(3)的上述熔融张力的最大值为0.15cN。 A1-B-A2 type triblock copolymer (SEBS triblock copolymer, styrene content is 20% by weight, ethylene-butylene content is 80% by weight, and the weight average molecular weight of A1, A2 is 9400 , The weight average molecular weight of B is 75200) 100% by weight is used as a triblock copolymer (3). The maximum value of the aforementioned melt tension of the triblock copolymer (3) was 0.15 cN.
[0204] A1-B-A2型三嵌段共聚物(4): A1-B-A2 type triblock copolymer ( 4 ):
[0205] 将A1’-B’-A2’型三嵌段共聚物(SEPS三嵌段共聚物,苯乙烯含量为30 重量%,乙烯-丙烯含量为70重量%,A1’、A2’的重均分子量为7500,B’的重均分子量为35000)60重量%、和A1”-B”-A2”型三嵌段共聚物(SEPS三嵌段共聚物,苯乙烯含量为18重量%,乙烯-丙烯含量为82重量%,A1”、A2”的重均分子量为8100,B”的重均分子量为73800)40重量%用亨舍尔混合机混合,将所得聚合物作为三嵌段共聚物〔4)使用。三嵌段共聚物(4)的上述熔融张力的最大值为0.20cN。 A1'-B'-A2' type triblock copolymer (SEPS triblock copolymer, styrene content is 30% by weight , ethylene-propylene content is 70% by weight, the weight of A1', A2' The average molecular weight is 7500, the weight average molecular weight of B' is 35000) 60% by weight, and A1 "-B"-A2" type triblock copolymer (SEPS triblock copolymer, styrene content is 18% by weight, ethylene -The propylene content is 82% by weight, the weight average molecular weight of A1", A2" is 8100, and the weight average molecular weight of B" is 73800) 40% by weight is mixed with a Henschel mixer, and the obtained polymer is used as a triblock copolymer (4) use. The maximum value of the melt tension of the triblock copolymer (4) was 0.20 cN.
三嵌段共聚物(4)中聚合物嵌段A1的重均分子量为:[(聚合物嵌段A1’的重均分子量)×(该A1’-B’-A2’在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)+(聚合物嵌段A1”的重均分子量)×(该A1”-B”-A2”在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)=]7740。 The weight-average molecular weight of the polymer block A1 in the triblock copolymer (4) is: [(the weight-average molecular weight of the polymer block A1') × (the A1'-B'-A2' contained in the resin composition The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers)+(the weight-average molecular weight of the polymer block A1″)×(the A1″-B″-A2 "The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers contained in the resin composition) =] 7740. the
三嵌段共聚物(4)中聚合物嵌段B的重均分子量为:[(聚合物嵌段B’的重均分子量)×(该A1’-B’-A2’在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)+(聚合物嵌段B”的重均分子量)×(该A1”-B”-A2”在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)=]50520。 The weight-average molecular weight of polymer block B in the three-block copolymer (4) is: [(the weight-average molecular weight of polymer block B') * (the A1 '-B'-A2 ' contained in the resin composition The percentage of the total amount of two or more A1-B-A2 type triblock copolymers)+(the weight-average molecular weight of the polymer block B ")×(the A1"-B"-A2 "The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers contained in the resin composition) =] 50520. the
三嵌段共聚物(4)中聚合物嵌段A2的重均分子量为:[(聚合物嵌段A2’的重均分子量)×(该A1’-B’-A2’在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的含量)+(聚合物嵌段A2”的重均分子量)×(该A1”-B”-A2”在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)=]7740。 The weight-average molecular weight of the polymer block A2 in the triblock copolymer (4) is: [(the weight-average molecular weight of the polymer block A2') × (the A1'-B'-A2' contained in the resin composition The content in the total amount of two or more A1-B-A2 type triblock copolymers)+(the weight average molecular weight of the polymer block A2 ") × (the A1 "-B"-A2 "in The percentage content of the total amount of two or more A1-B-A2 type triblock copolymers contained in the resin composition =] 7740. the
[0209] A1-B-A2型三嵌段共聚物(5): A1-B-A2 type triblock copolymer ( 5 ):
将A1’-B’-A2’三嵌段型共聚物(SEPS三嵌段共聚物,苯乙烯含量为30重量%,乙烯-丙烯含量为70重量%,A1’、A2’的重均分子量为7500,B’的重均分子量为35000)50重量%、和A1”-B”-A2”型三嵌段共聚物(SEPS三嵌段共聚物,苯乙烯含量为30重量%,乙烯-丙烯含量为70重量%,A1”、A2”的重均分子量为10500,B”的重均分子量为49000)50重量%用亨舍尔混合机混合,将所得聚合物作为三嵌段共聚物(5)使用。三嵌段共聚物(5)的上述熔融张力的最大值为0.07cN。 A1'-B'-A2' triblock type copolymer (SEPS triblock copolymer, styrene content is 30% by weight, ethylene-propylene content is 70% by weight, the weight average molecular weight of A1', A2' is 7500, the weight average molecular weight of B' is 35000) 50% by weight, and A1 "-B"-A2" type triblock copolymer (SEPS triblock copolymer, styrene content is 30% by weight, ethylene-propylene content 70% by weight, the weight average molecular weight of A1", A2" is 10500, and the weight average molecular weight of B" is 49000) 50% by weight is mixed with a Henschel mixer, and the resulting polymer is used as a triblock copolymer (5) use. The maximum value of the melt tension of the triblock copolymer (5) was 0.07 cN. the
三嵌段共聚物(5)中聚合物嵌段A1的重均分子量为:[(聚合物嵌段 A1’的重均分子量)×(该A1’-B’-A2’在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)+(聚合物嵌段A1”的重均分子量)×(该A1”-B”-A2”在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)=]9000。 The weight-average molecular weight of the polymer block A1 in the triblock copolymer (5) is: [(the weight-average molecular weight of the polymer block A1') × (the A1'-B'-A2' contained in the resin composition The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers)+(the weight-average molecular weight of the polymer block A1″)×(the A1″-B″-A2 "The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers contained in the resin composition) =] 9000. the
三嵌段共聚物(5)中聚合物嵌段B的重均分子量为:[(聚合物嵌段B’的重均分子量)×(该A1’-B’-A2’在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)+(聚合物嵌段B”的重均分子量)×(该A1”-B”-A2”在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)=]42000。 The weight-average molecular weight of polymer block B in the three-block copolymer (5) is: [(the weight-average molecular weight of polymer block B') * (the A1 '-B'-A2 ' contained in the resin composition The percentage of the total amount of two or more A1-B-A2 type triblock copolymers)+(the weight-average molecular weight of the polymer block B ")×(the A1"-B"-A2 "The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers contained in the resin composition) =] 42000. the
三嵌段共聚物(5)中聚合物嵌段A2的重均分子量为:[(聚合物嵌段A2’的重均分子量)×(该A1’-B’-A2’在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)+(聚合物嵌段A2”的重均分子量)×(该A1”-B”-A2”在树脂组合物所含的2种以上的A1-B-A2型三嵌段共聚物的总量中所占的百分含量)=]9000。 The weight-average molecular weight of the polymer block A2 in the triblock copolymer (5) is: [(the weight-average molecular weight of the polymer block A2') × (the A1'-B'-A2' contained in the resin composition The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers)+(the weight-average molecular weight of the polymer block A2")×(the A1"-B"-A2 "The percentage content in the total amount of two or more A1-B-A2 type triblock copolymers contained in the resin composition) =] 9000. the
[0214] A1-B-A2型三嵌段共聚物(6): A1-B-A2 type triblock copolymer ( 6 ):
[0215] 将A1-B-A2型三嵌段共聚物(SEPS三嵌段共聚物,苯乙烯含量为30重量%,乙烯-丙烯含量为70重量%,A1、A2的重均分子量为10500,B的重均分子量为49000)100重量%作为三嵌段共聚物(6)使用。三嵌段共聚物(6)的上述熔融张力的最大值为0.08cN。 By A1-B-A2 type triblock copolymer (SEPS triblock copolymer, styrene content is 30% by weight, ethylene-propylene content is 70% by weight, the weight average molecular weight of A1, A2 is 10500, The weight average molecular weight of B is 49000) 100% by weight was used as a triblock copolymer (6). The above-mentioned maximum value of the melt tension of the triblock copolymer (6) was 0.08 cN.
[0216] A1-B-A2型三嵌段共聚物(7): A1-B-A2 type triblock copolymer ( 7 ):
[0217] 将A1-B-A2型三嵌段共聚物(SEBS三嵌段共聚物,苯乙烯含量为20重量%,乙烯-丁烯含量为80重量%,A1、A2的重均分子量为4750,B的重均分子量为38000)100重量%作为三嵌段共聚物(7)使用。三嵌段共聚物(7)的上述熔融张力的最大值为0.05cN。 A1-B-A2 type triblock copolymer (SEBS triblock copolymer, styrene content is 20% by weight, ethylene-butylene content is 80% by weight, and the weight average molecular weight of A1, A2 is 4750 , The weight average molecular weight of B is 38000) 100% by weight is used as a triblock copolymer (7). The maximum value of the aforementioned melt tension of the triblock copolymer (7) was 0.05 cN.
[0218] A1-B-A2型三嵌段共聚物(8): A1-B-A2 type triblock copolymer ( 8 ):
[0219] 将A1-B-A2型三嵌段共聚物(SEPS三嵌段共聚物,苯乙烯含量为30重量%,乙烯含量为70重量%,A1、A2的重均分子量为22750,B的重均分子量为84500)100重量%作为三嵌段共聚物(8)使用。如图4所示测定了熔融张力,但由于粘度高,无法挤出,因此未能测得。 By A1-B-A2 type triblock copolymer (SEPS triblock copolymer, styrene content is 30% by weight, ethylene content is 70% by weight, the weight average molecular weight of A1 , A2 is 22750, B's The weight average molecular weight was 84500) and 100% by weight was used as the triblock copolymer (8). Melt tension was measured as shown in Fig. 4, but it could not be measured because the viscosity was high and it could not be extruded.
[评价] [evaluate]
将实施例和比较例中所得的复合体19(弹性长丝13)的特性与树脂组合物(弹性长丝13的形成材料)的组成一并示于下述表2及表3中。表2及表3中各项目的测定方法如下所述。 The properties of the composite 19 (elastic filament 13 ) obtained in Examples and Comparative Examples are shown in Table 2 and Table 3 below together with the composition of the resin composition (material for forming the elastic filament 13 ). The measurement method of each item in Table 2 and Table 3 is as follows. the
<弹性长丝的纺丝成形性> <Spinning Formability of Elastic Filament>
将作为弹性长丝的形成材料的树脂组合物(上述三嵌段共聚物(1)~(8))在以245℃的温度加热熔融的状态下,从内径为0.45mm、长度为4.5mm的圆筒形状的喷嘴孔中以8.4m/分钟的喷出速度如图4所示地喷出,制成长丝,在设置于从该喷嘴孔向下方100mm的位置处的不锈钢板上采集该长丝。将所采集的长丝不断裂地连续、且用显微镜放大200倍观察该长丝时长丝的侧面是平滑的情况评价为○(纺丝成形性良好),将长丝断裂而不连续的情况或长丝由于离模膨胀而粗细度变得不均匀的情况评价为×。 In the state where the resin composition (the above-mentioned triblock copolymers (1) to (8)) serving as the forming material of the elastic filament was heated and melted at a temperature of 245° C., the In the cylindrical nozzle hole, it is sprayed as shown in FIG. 4 at a spray speed of 8.4 m/min to make a long filament, and the long filament is collected on a stainless steel plate arranged at a position 100 mm downward from the nozzle hole. . The case where the collected filaments are continuous without breaking and the sides of the filaments are smooth when observed with a microscope at 200 times magnification is evaluated as ○ (spinning formability is good), and the cases where the filaments are broken and discontinuous or long The case where the thickness of the yarn became non-uniform due to die swell was evaluated as x. the
<曲折状态> <bending state>
从实施例及比较例中所得的复合体中,沿机械移动方向(MD方向、复合体制造时该复合体的移动方向)采样30cm,透过覆盖该弹性长丝的无纺布目测观察弹性长丝的曲折状态。将相邻100根弹性长丝中交叉或接触的长丝为10根以内的情况评价为○,将其中11根以上交叉或接触的情况评价为×。 From the composites obtained in Examples and Comparative Examples, 30 cm was sampled along the mechanical movement direction (MD direction, the moving direction of the composite during composite manufacture), and the elastic length was visually observed through the nonwoven fabric covering the elastic filaments. The tortuosity of the wire. Among 100 adjacent elastic filaments, the case where less than 10 intersected or contacted the elastic filaments was evaluated as ○, and the case where 11 or more intersected or contacted among them was evaluated as x. the
<防尿布偏移掉落性> <Diaper deflection and drop resistance>
对实施例及比较例中所得的复合体使用具备图7所示的一对齿槽辊的拉伸装置实施拉伸处理,制作图1及图2所示的伸缩片材,将其用作尿布的外包装材料,制作腰部的周长为35cm的短裤型一次性尿布。如图9所示,将该尿布穿在周长为44cm的丙烯酸管上,将尿布下部用鳄口夹固定,使该夹子朝向上侧移动,将丙烯酸管置于千斤顶上。此时,在丙烯酸管上标记尿布的腰部位置(将此时的位置作为初始位置A),在固定夹子的情况下将千斤顶下降50mm。测定将千斤顶下降50mm后的腰部位置(将此时的位置作为偏移位置)和初始位置A之间的距离,将该距离作为尿布的偏移掉落量。将该偏移掉落量小于10mm的情况判定为◎(防尿布偏移掉落性非常好)、将10mm以上但小于20mm的情况判定为○(防尿布偏移掉落性良好)、将20mm以上但小于30mm的情况判定为△(实际应用上没问题的水平)、将30mm以上的情况判定为×。 The composites obtained in Examples and Comparative Examples were stretched using a stretching device equipped with a pair of toothed rollers as shown in Fig. 7 to produce stretchable sheets as shown in Figs. 1 and 2, which were used as diapers Outer packaging materials, making a shorts-type disposable diaper with a waist circumference of 35cm. As shown in Fig. 9, the diaper was put on an acrylic tube having a circumference of 44 cm, the lower part of the diaper was fixed with an alligator clip, the clip was moved upward, and the acrylic tube was placed on a jack. At this time, the waist position of the diaper was marked on the acrylic tube (the position at this time was defined as initial position A), and the jack was lowered by 50 mm while the clip was fixed. The distance between the waist position after the jack was lowered by 50 mm (the position at this time was defined as the offset position) and the initial position A was measured, and this distance was defined as the offset drop amount of the diaper. The case where the amount of this deviation and drop is less than 10 mm is judged as ◎ (prevention of diaper deviation and drop is very good), the case of 10 mm or more but less than 20 mm is judged as ○ (diaper deviation and drop resistance is good), and the case of 20 mm The case of more than 30 mm but less than 30 mm was judged as Δ (a level that is practically no problem), and the case of 30 mm or more was judged as ×. the
由表2及表3所示的结果可知,实施例2-1~2-5由于均使用了本发明范围内的树脂组合物,因此长丝的纺丝成形性优异,在伸缩片材中长丝没有曲折,将伸缩片材用于尿布时,可以获得难以偏移掉落的尿布。与此相对,在比较例2-1中,由于离模膨胀使长丝的粗细度变得不均匀,长丝从变得非常细的部分断裂,无法获得连续长丝。在比较例2-2中,虽然粗细度均匀,但熔融张力低,因此长丝断裂,无法获得连续长丝。因而,在将比较例2-1及2-2中获得的伸缩片材用于尿布时,由于长丝的断裂导致伸缩特性降低,因此偏移掉落性变差。在比较例2-3中,由于三嵌段共聚物(8)的粘度高,无法纺丝成形,因此无法获得长丝。 From the results shown in Table 2 and Table 3, it can be seen that since Examples 2-1 to 2-5 all used the resin composition within the scope of the present invention, the spinning formability of the filament was excellent, and it was long in the stretch sheet. There are no twists and turns in the thread, and when the stretch sheet is used for diapers, it is possible to obtain a diaper that is difficult to fall off. On the other hand, in Comparative Example 2-1, the thickness of the filaments became non-uniform due to the die swell, and the filaments were broken from the very thin portions, so that continuous filaments could not be obtained. In Comparative Example 2-2, although the thickness was uniform, the melt tension was low, so the filaments were broken and continuous filaments could not be obtained. Therefore, when the stretch sheets obtained in Comparative Examples 2-1 and 2-2 were used for diapers, the stretching properties were lowered due to the breakage of the filaments, so that the deflection drop property deteriorated. In Comparative Example 2-3, since the viscosity of the triblock copolymer (8) was high, it could not be spun and formed, so a filament could not be obtained. the
[实施例3-1] [Example 3-1]
使用图5所示的装置制造图1及图2所示结构的伸缩片材。作为第1及第2无纺布11、12,使用单位面积重量为20g/m2、纤维密度为0.074g/cm3的热风法无纺布。该无纺布的构成纤维是直径为19μm、最大伸长率为180%、纤维长度为44mm的芯鞘型复合纤维(芯:PET;鞘:PE)。作为弹性长丝13的原料树脂,使用由SEPS树脂(重均分子量为5万;MFR为60g/10分钟(230℃、2.16kg))构成的弹性体。纺丝条件是:纺丝头17的温度为310℃、纺丝喷嘴16的直径为400μm、纺丝喷嘴16的间距为1mm、拉伸倍率为11倍。弹性长丝13的直径为107μm。长丝的单位面积重量为8g/m2。在弹性长丝和无纺布11、12的接合中设置夹持辊间的间隔W,并将该间隔设为0.2mm。夹持辊中一个使用金属平辊,另一个使用橡胶辊。复合体19的拉伸加工使用具备在轴长方向上交替形成有齿和齿沟的一对齿槽辊20、21的拉伸装置22来进行。齿间及齿沟间的间距分别为2.0mm(在啮合状态下的齿间的间距P为1.0mm)。调整上下的齿槽辊的压入量,以拉伸倍率为3.0倍使复合体19在弹性长丝13的延伸方向上拉伸。由此获得在弹性长丝13的延伸方向上伸缩的单位面积重量为48g/m2的伸缩片材10。所得伸缩片材10透过无纺布呈现弹性长丝13产生的条纹花样。另外还呈现高单位面积重量区域及低单位面积重量区域产生的条纹花样。通过这两种条纹花样,伸缩片材还呈现格子状的花样。另外,伸缩片材10中的弹性长丝13具有长轴在该片材10的平面方向上 的椭圆形截面,长轴/短轴之比为1.5。1.5倍伸长时的宽度减缩为4%。
The stretch sheet having the structure shown in Fig. 1 and Fig. 2 was manufactured using the apparatus shown in Fig. 5 . As the first and second
[实施例3-2~3-4] [Example 3-2~3-4]
将夹持辊间的间隔W设为表4及表5所示的值,除此以外,与实施例3-1同样操作,获得伸缩片材10。
A
[实施例3-5~3-7] [Example 3-5~3-7]
将从纺丝喷嘴的顶端到接合前的距离设为表4及表5所示值,并在接合中不设置夹持辊的间隔地进行整面挤压,除此以外,与实施例3-1同样操作,获得伸缩片材10。
Except that the distance from the tip of the spinning nozzle to before joining is set to the values shown in Table 4 and Table 5, and the entire surface extrusion is performed without gaps between nip rolls during joining, the same as in Example 3- 1. Perform the same operation to obtain a
[比较例3-1] [Comparative Example 3-1]
使用从T模挤出的薄膜状的弹性树脂代替弹性长丝,并将该薄膜状弹性树脂与无纺布进行层叠,除此以外,与实施例3-1同样操作,获得伸缩片材。作为该弹性树脂,使用G1657(商品名、Kraton Polymers制)。 A stretch sheet was obtained in the same manner as in Example 3-1 except that a film-like elastic resin extruded from a T-die was used instead of the elastic filaments, and the film-like elastic resin was laminated on a nonwoven fabric. As the elastic resin, G1657 (trade name, manufactured by Kraton Polymers) was used. the
[评价] [evaluate]
对实施例及比较例中得到的伸缩片材,测定并评价了表4及表5所示的各项目。表4及表5中的“层间剥离强度”(弹性长丝与无纺布之间的接合强度)、“25%回复强度(cN/{50mm·(g/m2)})”(单位伸缩片材中所含弹性树脂的单位面积重量的25%回复强度)、“弹性长丝与无纺布构成纤维之间的平均接合比例”、“宽度减缩(%)”(将伸缩片材伸长到1.5倍时的宽度减缩)、以及伸缩片材及无纺布的厚度分别通过上述的方法来测定。另外,“25%回复强度(cN/50mm)”、“25%回复强度/25%伸长强度(%)”、及“手感”分别通过以下的方法来测定和评价。另外,“弹性长丝的交叉”通过目测观察进行。几乎观察不到弹性长丝的交叉的情况为最高评价、有交叉的情况为低评价。 Each item shown in Table 4 and Table 5 was measured and evaluated about the stretch sheet obtained in the Example and the comparative example. In Table 4 and Table 5, "interlaminar peel strength" (bonding strength between elastic filament and nonwoven fabric), "25% recovery strength (cN/{50mm·(g/m 2 )})" (unit 25% recovery strength per unit area weight of the elastic resin contained in the stretch sheet), "average bonding ratio between elastic filaments and non-woven fabric constituting fibers", "width reduction (%)" (stretch the stretch sheet Width reduction when 1.5 times longer), and the thickness of the stretch sheet and nonwoven fabric were measured by the above-mentioned methods, respectively. In addition, "25% recovery strength (cN/50mm)", "25% recovery strength/25% elongation strength (%)", and "touch" were measured and evaluated by the following methods, respectively. In addition, "intersection of elastic filaments" was performed by visual observation. The case where the intersection of the elastic filaments was hardly observed was the highest evaluation, and the case where the intersection was observed was the low evaluation.
[25%回复强度/25%伸长强度、25%回复强度] [25% Recovery Strength/25% Elongation Strength, 25% Recovery Strength]
将伸缩片材按其伸缩方向上为200mm、与该伸缩方向垂直的方向上为50mm的大小切出试验片。在牵拉试验机(岛津制作所制Autograph AG-1kNIS)上以夹头间距离(初始长度)为150mm安装固定试验片。使试验片在其伸缩 方向上以300mm/分钟的速度伸长,记录伸长25%时的负荷,将该值作为25%伸长强度。继续使试验片伸长到50%,然后立即使其向回复方向(收缩方向)以相同速度收缩,记录伸长初始长度的25%时的负荷,将其作为25%回复强度。使用分别由此求得的25%伸长强度的值及25%回复强度的值,算出25%回复强度/25%伸长强度(%)。以上测定是在温度为20±2℃、湿度为65±5%RH的环境下进行的。 A test piece is cut out from the stretchable sheet to a size of 200 mm in the stretching direction and 50 mm in a direction perpendicular to the stretching direction. A test piece was mounted and fixed on a tensile tester (Autograph AG-1kNIS manufactured by Shimadzu Corporation) so that the distance between chucks (initial length) was 150 mm. Make the test piece elongate at a rate of 300 mm/min in the stretching direction, record the load at the time of 25% elongation, and use this value as the 25% elongation strength. Continue to stretch the test piece to 50%, then immediately shrink it in the recovery direction (shrinkage direction) at the same speed, and record the load when it is stretched to 25% of the initial length, and use it as the 25% recovery strength. Using the values of the 25% elongation strength and the 25% recovery strength thus obtained, respectively, 25% recovery strength/25% elongation strength (%) was calculated. The above measurements are carried out in an environment with a temperature of 20±2° C. and a humidity of 65±5% RH. the
[手感] [feel]
让女性评价者10人在看不见伸缩片材的暗箱内、在温度为25℃、湿度为40%的环境下对所述该伸缩片材的手感进行评价。根据各评价者的评价,用下述分数进行打分,然后以评价者10人的平均分数(小数点以下四舍五入)作为手感的评价分数。 Ten female evaluators evaluated the feel of the stretch sheet in an environment with a temperature of 25° C. and a humidity of 40% in a dark box where the stretch sheet could not be seen. Based on the evaluation by each evaluator, the following points were used for scoring, and the average score (rounded up to one decimal point) of 10 evaluators was used as the evaluation score of texture. the
5分:手感好。 5 points: Feel good. the
4分:手感稍好。 4 points: Feeling is slightly better. the
3分:一般。 3 points: average. the
2分:手感稍差。 2 points: Feeling slightly poor. the
1分:手感差。 1 point: The hand feeling is poor. the
表4 Table 4
表5 table 5
由表4及表5所示的结果可知,各实施例的伸缩片材均显示所希望的平均接合比例,具有较高的层间剥离强度(弹性长丝与无纺布之间的接合强度)和较高的25%回复强度(伸缩片材中的弹性树脂的每单位面积重量的25%回复强度),宽度减缩小,基本观察不到弹性长丝的交叉,手感也优异。另外,各实施例的伸缩片材具有图2所示的外观,外观也良好。与此相对,比较例3-1的伸缩片材中的弹性树脂的每单位面积重量的25%回复强度低、宽度减缩大、也没有透气性。 From the results shown in Table 4 and Table 5, it can be seen that the stretch sheets of each embodiment show the desired average bonding ratio, and have a higher interlayer peel strength (bonding strength between the elastic filament and the nonwoven fabric) And high 25% recovery strength (25% recovery strength per unit area weight of the elastic resin in the stretch sheet), the width reduction is small, the intersection of elastic filaments is hardly observed, and the hand feeling is also excellent. In addition, the stretch sheet of each Example had the appearance shown in FIG. 2, and the appearance was also favorable. In contrast, the elastic resin in the stretch sheet of Comparative Example 3-1 had a low 25% recovery strength per unit area weight, a large width reduction, and no air permeability. the
如上所述,在本发明的伸缩片材中,由于弹性长丝沿一个方向延伸地排列,因此可以在不发生宽度减缩的情况下使该伸缩片材沿该弹性长丝的延伸方向伸长。另外,本发明的伸缩片材的强度高,在使伸缩片材伸长时,不容易引起弹性长丝与无纺布的剥离。 As described above, in the stretchable sheet of the present invention, since the elastic filaments are arranged to extend in one direction, the stretchable sheet can be stretched in the direction in which the elastic filaments extend without reducing the width. In addition, the stretchable sheet of the present invention has high strength, and when the stretchable sheet is stretched, the elastic filaments and the nonwoven fabric are less likely to be peeled off. the
另外,在本发明的伸缩片材中,相对于含有非弹性纤维而构成的可伸长的无纺布,大量的弹性长丝沿一个方向延伸地排列,且弹性长丝与该无纺布之间的接合强度、伸缩片材中的弹性树脂的每单位面积重量的25%回复强度、及弹性长丝与构成该无纺布的纤维之间的平均接合比例分别在上述特定的范围内,因此层间接合强度与伸缩特性之间的平衡性优异,可以在不发生宽度减缩的情况下使该伸缩片材沿该弹性长丝的延伸方向伸长,而且,在使伸缩片材伸长时,不容易引起弹性长丝与无纺布的剥离。 In addition, in the stretchable sheet of the present invention, a large number of elastic filaments are arranged to extend in one direction with respect to an extensible nonwoven fabric composed of non-elastic fibers, and the elastic filaments and the nonwoven fabric The bonding strength between them, the 25% recovery strength per unit area weight of the elastic resin in the stretch sheet, and the average bonding ratio between the elastic filaments and the fibers constituting the nonwoven fabric are respectively within the above-mentioned specified ranges, so The balance between the interlayer joint strength and stretch properties is excellent, and the stretch sheet can be stretched along the extending direction of the elastic filaments without width reduction, and when the stretch sheet is stretched, It is not easy to cause peeling of elastic filaments and non-woven fabrics. the
另外,本发明的弹性长丝的纺丝成形性优异,即使在直径较细的情况下,也可以在不发生断丝且不发生曲折的情况下从纺丝喷嘴中喷出成形,可以进行高速生产。含有该弹性长丝构成的本发明的伸缩片材例如作为以一次性尿布等吸收性物品为代表的各种穿戴衣物、其它穿戴在人体上的各种物品的形成材料来使用时,由于该弹性长丝的作用,显示优异的合身性,可以有效地防止穿戴衣物的偏移掉落。含有该伸缩片材而构成的本发明的吸收性物品具有优异的穿戴过程中的合身性,且难以偏移掉落。 In addition, the elastic filament of the present invention has excellent spinning formability, and can be ejected from the spinning nozzle without breaking or twisting even in the case of a small diameter, and can be processed at high speed. Production. When the elastic sheet of the present invention composed of such elastic filaments is used, for example, as a forming material of various kinds of clothing represented by absorbent articles such as disposable diapers, and other various articles worn on the human body, due to the elasticity The role of the filaments, showing excellent fit, can effectively prevent the deviation of wearing clothes from falling. The absorbent article of the present invention comprising the stretchable sheet has excellent fit during wearing and is difficult to fall off. the
Claims (18)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP356560/2006 | 2006-12-28 | ||
| JP2006356560 | 2006-12-28 | ||
| JP2007192665A JP5188117B2 (en) | 2007-07-24 | 2007-07-24 | Elastic filament and elastic sheet using the same |
| JP192665/2007 | 2007-07-24 | ||
| JP233410/2007 | 2007-09-07 | ||
| JP2007233410A JP4918002B2 (en) | 2007-09-07 | 2007-09-07 | Elastic sheet and method for producing the same |
| PCT/JP2007/072871 WO2008081662A1 (en) | 2006-12-28 | 2007-11-27 | Stretchable sheet and process for producing the stretchable sheet |
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| Publication Number | Publication Date |
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| CN101557929A CN101557929A (en) | 2009-10-14 |
| CN101557929B true CN101557929B (en) | 2012-09-05 |
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| CN200780045872.8A Expired - Fee Related CN101557929B (en) | 2006-12-28 | 2007-11-27 | Stretchable sheet and process for producing the stretchable sheet |
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| CN101557929A (en) | 2009-10-14 |
| JP2008179128A (en) | 2008-08-07 |
| JP5063315B2 (en) | 2012-10-31 |
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