US3458271A - Simultaneous aminoplast impregnation and direct dyeing by the pad dwell process followed by hot curing of the aminoplast - Google Patents
Simultaneous aminoplast impregnation and direct dyeing by the pad dwell process followed by hot curing of the aminoplast Download PDFInfo
- Publication number
- US3458271A US3458271A US603733A US3458271DA US3458271A US 3458271 A US3458271 A US 3458271A US 603733 A US603733 A US 603733A US 3458271D A US3458271D A US 3458271DA US 3458271 A US3458271 A US 3458271A
- Authority
- US
- United States
- Prior art keywords
- aminoplast
- padded
- fabric
- dyeing
- dyes
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 32
- 229920003180 amino resin Polymers 0.000 title claims description 11
- 238000005470 impregnation Methods 0.000 title description 3
- 238000009967 direct dyeing Methods 0.000 title 1
- 239000000835 fiber Substances 0.000 claims description 23
- 239000003795 chemical substances by application Substances 0.000 claims description 21
- 238000004043 dyeing Methods 0.000 claims description 20
- 239000000982 direct dye Substances 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 6
- 239000003377 acid catalyst Substances 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 5
- 238000001704 evaporation Methods 0.000 claims description 5
- 230000008020 evaporation Effects 0.000 claims description 5
- 239000002657 fibrous material Substances 0.000 claims description 4
- 239000002243 precursor Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 claims 1
- 238000004326 stimulated echo acquisition mode for imaging Methods 0.000 claims 1
- 239000004744 fabric Substances 0.000 description 30
- 239000000975 dye Substances 0.000 description 17
- 229920005989 resin Polymers 0.000 description 17
- 239000011347 resin Substances 0.000 description 17
- 239000000203 mixture Substances 0.000 description 16
- 229920000297 Rayon Polymers 0.000 description 15
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000002964 rayon Substances 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 238000005406 washing Methods 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 238000013508 migration Methods 0.000 description 5
- 230000005012 migration Effects 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- VGGLHLAESQEWCR-UHFFFAOYSA-N N-(hydroxymethyl)urea Chemical compound NC(=O)NCO VGGLHLAESQEWCR-UHFFFAOYSA-N 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 230000002940 repellent Effects 0.000 description 3
- 239000005871 repellent Substances 0.000 description 3
- 244000025254 Cannabis sativa Species 0.000 description 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 229920001407 Modal (textile) Polymers 0.000 description 2
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical compound NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- -1 amino - Chemical class 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 235000009120 camo Nutrition 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 235000005607 chanvre indien Nutrition 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000011487 hemp Substances 0.000 description 2
- 150000003840 hydrochlorides Chemical class 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- GJRKKTVFRGJAFQ-UHFFFAOYSA-N prop-2-en-1-ol;urea Chemical compound NC(N)=O.OCC=C GJRKKTVFRGJAFQ-UHFFFAOYSA-N 0.000 description 2
- KANWMCHBSYQIEL-UHFFFAOYSA-N prop-2-ene-1,2-diol;urea Chemical compound NC(N)=O.OCC(O)=C KANWMCHBSYQIEL-UHFFFAOYSA-N 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- PMZIUAOBHNJYQT-UHFFFAOYSA-N (1-hydroxy-2-methylpropan-2-yl)azanium;chloride Chemical compound Cl.CC(C)(N)CO PMZIUAOBHNJYQT-UHFFFAOYSA-N 0.000 description 1
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
- ZVXPZLNAJOMRPK-UHFFFAOYSA-N 2-(hydroxymethyl)prop-1-ene-1,3-diol;urea Chemical compound NC(N)=O.OCC(CO)=CO ZVXPZLNAJOMRPK-UHFFFAOYSA-N 0.000 description 1
- JFFYKITVXPZLQS-UHFFFAOYSA-N 2-methylidenepropane-1,3-diol Chemical group OCC(=C)CO JFFYKITVXPZLQS-UHFFFAOYSA-N 0.000 description 1
- AOSPVUKRNAQARI-UHFFFAOYSA-N 2-n-(trimethoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COC(OC)(OC)NC1=NC(N)=NC(N)=N1 AOSPVUKRNAQARI-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241000322338 Loeseliastrum Species 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- UZZFFIUHUDOYPS-UHFFFAOYSA-L disodium 4-amino-3,6-bis[[4-[(2,4-diaminophenyl)diazenyl]phenyl]diazenyl]-5-oxido-7-sulfonaphthalene-2-sulfonate Chemical compound [Na+].[Na+].Nc1ccc(N=Nc2ccc(cc2)N=Nc2c(N)c3c(O)c(N=Nc4ccc(cc4)N=Nc4ccc(N)cc4N)c(cc3cc2S([O-])(=O)=O)S([O-])(=O)=O)c(N)c1 UZZFFIUHUDOYPS-UHFFFAOYSA-L 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 1
- 229950005308 oxymethurea Drugs 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000985 reactive dye Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- QTTDXDAWQMDLOF-UHFFFAOYSA-J tetrasodium 3-[[4-[[4-[(6-amino-1-hydroxy-3-sulfonatonaphthalen-2-yl)diazenyl]-6-sulfonatonaphthalen-1-yl]diazenyl]naphthalen-1-yl]diazenyl]naphthalene-1,5-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].Nc1ccc2c(O)c(N=Nc3ccc(N=Nc4ccc(N=Nc5cc(c6cccc(c6c5)S([O-])(=O)=O)S([O-])(=O)=O)c5ccccc45)c4ccc(cc34)S([O-])(=O)=O)c(cc2c1)S([O-])(=O)=O QTTDXDAWQMDLOF-UHFFFAOYSA-J 0.000 description 1
- XRFRTDKENRGSSX-UHFFFAOYSA-J tetrasodium;3-[[4-[[4-[(4,8-disulfonatonaphthalen-2-yl)diazenyl]-3-methylphenyl]carbamoylamino]-2-methylphenyl]diazenyl]naphthalene-1,5-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].C1=CC=C(S([O-])(=O)=O)C2=CC(N=NC3=CC=C(NC(=O)NC=4C=C(C)C(N=NC=5C=C6C(=CC=CC6=C(C=5)S([O-])(=O)=O)S([O-])(=O)=O)=CC=4)C=C3C)=CC(S([O-])(=O)=O)=C21 XRFRTDKENRGSSX-UHFFFAOYSA-J 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/56—Condensation products or precondensation products prepared with aldehydes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/916—Natural fiber dyeing
- Y10S8/918—Cellulose textile
Definitions
- This invention relates to a process for dyeing cellulosic fibers, and more particularly relates to a process for dyeling cellulosic fibers which comprises employing an amino -"resi, n-treating agent such as an a-m'inoplast precursor as an'accel'eraftor .fordireet dyes to effect concurrent level dyeing-a "resin It'reatment.
- an amino -"resi, n-treating agent such as an a-m'inoplast precursor as an'accel'eraftor .fordireet dyes to effect concurrent level dyeing-a "resin It'reatment.
- a process for dyeing cellulosic fibers which comprises padding a textile fabric with an aqueous solution of direct dyes containing amino resin treating agent and acid catalyst, and allowing the padded fabric to stand in (dwell) a wet statewhile suppressing the evaporation of water, Without immediately drying the fabric, to sufficiently dye the fabric, and then drying and baking the treated fabric to effect concurrent dyeing and resin treatment.
- Maintaining the padded fibers in a wet state while suppressing the evaporation of water permits level dyeing at a low temperature and in a short time, which has not been achieved by any previous known technique, and perfectly obviates the disadvantage caused by the migration of dyes.
- through dyeing is accomplished prior to a heating process while preventing the migration of the dyes, and the unevenness of the resultant dyeing caused by the migration of the dyes, which has been a problem ditficult to solve in the known art, can be obviated.
- part of direct color which has been loosely attached to the fibers may be fixed on the fibers owing to the condensation of the resin treating agent. Therefore, the up-take of the dyes reaches about 100 percent and a subsequent water washing, which has been required in any previous known technique, can be omitted.
- the fibers to which the process of the present invention can be applied include viscose rayon, cuprammonium rayon, polynosic rayon, cotton, hemp and the like in the form of yarn, fabrics, knitting or the like.
- Impregnation with treating liquid may be carried out by spraying, padding, a mangle or dipping.
- the use of direct dyes is effective, and the use of the other dyes is undesirable in that a uniform dyeing can not be obtained and the fastnesses of the resultant dyeing are also poor.
- Even if direct dyes 'are used it is important to thoroughly proceed with dyeing of the padded fibers in a wet state as in the present process. It is very dangerous to immediately subject the 3 padded fibers to a drying process since uneven dyeings may be given by such an operation.
- the other dyes have no affinity to cellulosics, and the dyeing can proceed no vfurther. This invention is limitted to only the dyeing with direct dyes.
- the dyes other than direct dyes have no atfinity to cellulosics, These dyes do not; make proper dyeing in the treating solution of this invention.
- the amino resin treating agents whichmay be employed in the process of the present invention include methylolurea, methylolmelamine, methylol ethylene urea, methylol hydroxyethylene urea, methylolurone and a methyl etherified product thereof or a mixture thereof. They may be employed singly or in combination in an amount necessary to give ,crease resistance, shrink resistance, shaping property," wash and wear property and the other effects of the resin on the fibrous material.
- the material may be immediately rolled up and' then wrapped in an airimpermeable sheet, for example,plastic sheet produced from synthetic materials such as' polyvinyl chloride, polyvinylidene chloride, polyar'nide,.polyester, polyolefin, polyacrylic resin, etc.
- an airimpermeable sheet for example, plastic sheet produced from synthetic materials such as' polyvinyl chloride, polyvinylidene chloride, polyar'nide,.polyester, polyolefin, polyacrylic resin, etc.
- plastic sheet produced from synthetic materials such as' polyvinyl chloride, polyvinylidene chloride, polyar'nide,.polyester, polyolefin, polyacrylic resin, etc.
- synthetic materials such as' polyvinyl chloride, polyvinylidene chloride, polyar'nide,.polyester, polyolefin, polyacrylic resin, etc.
- material may be either immediately packed in a box or.
- the time for -whichthe padded fibrous material is temperature.
- the maintenance time varies also according I to the kind of cellulosic substance to be .dyed.
- the maintenance time may be relatively short for cuprammonium rayon, while it should be relatively long for cotton.
- urea-formaldehyde resin treating agent or a melamineformaldehyde resin treating agent it is possible to improve the crease resistance of the dyed fabric in a wet state and to improve the wash'and wear property of the fabric by allowing the padded fabric for a short period of time at to C. or overnight at room temperature.
- conventional softner or water repellents may be employed together with the resin treating agent.
- the acid catalyst should not be one which may cause the aggregation of the color followed by its precipitation which makes impossible a uniform impregnation of dyes.
- the catalysts of high acidity therefore, are not desirable.
- the most preferableacid.catalysts which may be used in the process of the present inven- Patentied July 1969 tion are hydrochlorides of organic amines and zinc nitrate and a mixture thereof.
- the baking may be carried out under customary resin treatment conditions. For example, it may be carried out at 120 to 150 C. for 3 to 8 minutes. If the baking is carried out with superheated steam, it is possible to improve further the fastnesses of a heavy color dyeing.
- the present invention is illustrated but not limited by the following examples.
- fastness to washing was tested according to 118 (Japanese Industrial Standards) L-1045 corresponding to ISO Method MC-2, and fastness to rubbing according to 11$ L-l048 corresponding to AATCC 84961, Crock-meter method, and crease resistance according to I18 L-1003 corresponding to AATCC 664959, Clerks method.
- Example 1 A hank of cuprammonium rayon of 75 deniers/54 filaments was immersed for one minute in a treating solution having the following composition:
- a direct black dye Resin treating agent 1 200 Zinc nitrate 5 N-octadecyl-N-ethylene nrea 2 8 1
- the resin treating agent was prepared by adding 5% sodium hydroxide to 1.540 cc. of 40% formalin 'to give a pH of S and then adding one kg. of urea thereto and heating the mixture at 80 C. for minutes with stirring and cooling the resultant product.
- the material is a softener and water repellent.
- the treated hank was immediately centrifuged and then wrapped in a vinyl chloride sheet. After standing at room temperature for two hours, the hank was dried at 70 C.
- a taffeta was woven by employing the above dyed yarn as warp and then baked at 140 C. for four minutes.
- Scoured 100 deniers/ filaments viscose rayon taffeta was padded with a treating solution having the following composition G./l.
- a direct blue dye 1 1O Resin treating agent 180 Zinc nitrate 5 The padded fabric obtained 72% wet pick-ups and is immediately rolled up and wrapped in a vinyl chloride sheet. After standing at room temperature for two hours, the treated fabric was dried at 80 C. and then baked at 140 C. for five minutes.
- the treating agent was prepared by adding 8 cc. of 5 percent sodium hydroxide to 800 cc. of 40 percent formalin to give a pH of 9 and then adding 500 grams of melamine thereto and heating the mixture at 80 C. for 30 minutes and cooling the resultant product.
- Example 6 Scoured viscose rayon staple fiber muslin fabric was padded at room temperature with a treating solution having the following composition:
- G./l. Cl. Direct Blue 71 (Cl. 34,140 15 Trimethylolmelamine Zinc nitrate 5
- the wet pick-ups of the padded fabric regulated 85% of the dried fabric, and is immediately rolled up and wrapped in a vinyl chloride sheet. After standing at room temperature for 12 hours, the fabric was dried at 70 C. and then baked at 140 C. for four minutes. Thus a uniformly dyed fabric was obtained having a good wet crease resistance and a fastness to washing of grade 5.
- Example 7 A cake of 75 deniers/33 filaments viscose rayon was charged into a cake dyeing machine, and a treating solution having the following composition:
- Example 8 6,000 ends of cuprammonium rayon yarns of 75 deniers/54 filaments which had been warped on a beam, was padded in 80 percent wet pick-up with a treating solution having the following composition:
- a process for concurrent dyeing and resin treatment comprising the steps of:
- said cellulose fiber is selected from the group consisting of viscose rayon, cuprammonium rayon, polynosic rayon, cotton, and hemp fibers.
- said amino resin treating agent is selected from the group consisting of methylolurea, methylolmelamine, methylol ethylene urea, methylol hydroxyethylene urea, inethylolurone and methyl etherified products thereof and a mixture thereof.
- said acid catalyst is selected from the group consisting of hydrochlorides of organic amines and zinc nitrate and a mixture thereof.
- said aqueous solution of a direct color further contains a conventional fiber softener or water repellent.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
United States Patent This invention relates to a process for dyeing cellulosic fibers, and more particularly relates to a process for dyeling cellulosic fibers which comprises employing an amino -"resi, n-treating agent such as an a-m'inoplast precursor as an'accel'eraftor .fordireet dyes to effect concurrent level dyeing-a "resin It'reatment.
- The us of reactive dyes, acid dyes, basic dyes or the likehas, heretofore proposed inIorder-to concurrently 'elfect-bothfdyeing and'resin treatment. However, according to anyqof' these. techniques, it {has been very difficult to "obtain leveldyeing since the resulting dyeings have 1 become uneven'by various causes.--For-example, there have been found' the migration ofjthe dyes to the surface of textile fabrics caused by the migration of water in a drying pro'c'ess,"the unevenness'at a selv'age formed in a tentering process, the unevenness forrned by heating,
etc. As non-substantive dyes have been fixed with an amino resin for-resin treatment in such techniques, the dyes as well as. the resin. have been released by washing, and'it has been impossible to obtain a dyeing of good fastnesses.
Accordingtothe present invention, there is provided a process for dyeing cellulosic fibers which comprises padding a textile fabric with an aqueous solution of direct dyes containing amino resin treating agent and acid catalyst, and allowing the padded fabric to stand in (dwell) a wet statewhile suppressing the evaporation of water, Without immediately drying the fabric, to sufficiently dye the fabric, and then drying and baking the treated fabric to effect concurrent dyeing and resin treatment.
When cellulosic fibers are padded with an aqueous solution of a direct dye and the padded fibers are allowed to stand at room temperature, it takes about 24 hours to approach adsorption equilibrium. However, if an amino resin treating agent is added thereto, the time required to approach adsorbtion equilibrium may be reduced to only one to two hours and a high degree dye absorption (dye up-take) can be obtained.
The reason why such an accelerating effect is obtained by the addition of the amino resin treating agent has not been sufficiently explained. The facts that the diffusion of the dye is facilitated by the improved swelling of the cellulosic fibers and that the diffusion of direct dyes is improved by the interaction of the amino resin treating agent having a very rapid diffusion rate are considered as the reason for this.
Maintaining the padded fibers in a wet state while suppressing the evaporation of water permits level dyeing at a low temperature and in a short time, which has not been achieved by any previous known technique, and perfectly obviates the disadavantage caused by the migration of dyes. According to the process of the present invention, through dyeing is accomplished prior to a heating process while preventing the migration of the dyes, and the unevenness of the resultant dyeing caused by the migration of the dyes, which has been a problem ditficult to solve in the known art, can be obviated.
By subjecting the fibers thus treated to a baking process, part of direct color which has been loosely attached to the fibers may be fixed on the fibers owing to the condensation of the resin treating agent. Therefore, the up-take of the dyes reaches about 100 percent and a subsequent water washing, which has been required in any previous known technique, can be omitted.
The fibers to which the process of the present invention can be applied include viscose rayon, cuprammonium rayon, polynosic rayon, cotton, hemp and the like in the form of yarn, fabrics, knitting or the like.
Impregnation with treating liquid may be carried out by spraying, padding, a mangle or dipping. In the process of the present invention the use of direct dyes is effective, and the use of the other dyes is undesirable in that a uniform dyeing can not be obtained and the fastnesses of the resultant dyeing are also poor. Even if direct dyes 'are used, it is important to thoroughly proceed with dyeing of the padded fibers in a wet state as in the present process. It is very dangerous to immediately subject the 3 padded fibers to a drying process since uneven dyeings may be given by such an operation. The other dyes have no affinity to cellulosics, and the dyeing can proceed no vfurther. This invention is limitted to only the dyeing with direct dyes. The dyes other than direct dyes have no atfinity to cellulosics, These dyes do not; make proper dyeing in the treating solution of this invention.
wThe amino resin treating agents Whichmay be employed in the process of the present invention include methylolurea, methylolmelamine, methylol ethylene urea, methylol hydroxyethylene urea, methylolurone and a methyl etherified product thereof or a mixture thereof. They may be employed singly or in combination in an amount necessary to give ,crease resistance, shrink resistance, shaping property," wash and wear property and the other effects of the resin on the fibrous material.
In order to maintain the padded fibrous material in a wet state while suppressing the evaporation of'water, the material may be immediately rolled up and' then wrapped in an airimpermeable sheet, for example,plastic sheet produced from synthetic materials such as' polyvinyl chloride, polyvinylidene chloride, polyar'nide,.polyester, polyolefin, polyacrylic resin, etc. Alternatively, the
material may be either immediately packed in a box or.
immediately introduced into a room of high humidity.
The time for -whichthe padded fibrous materialis temperature. The maintenance time varies also according I to the kind of cellulosic substance to be .dyed. Thus the maintenance time may be relatively short for cuprammonium rayon, while it should be relatively long for cotton.
If a urea-formaldehyde resin treating agent or a melamineformaldehyde resin treating agent is employed, it is possible to improve the crease resistance of the dyed fabric in a wet state and to improve the wash'and wear property of the fabric by allowing the padded fabric for a short period of time at to C. or overnight at room temperature.
For the purpose of regulating the hand temper of the dyed fabric or imparting water resisting property to the fabric, conventional softner or water repellents may be employed together with the resin treating agent.
The acid catalyst should not be one which may cause the aggregation of the color followed by its precipitation which makes impossible a uniform impregnation of dyes. The catalysts of high acidity, therefore, are not desirable. We have found that the most preferableacid.catalysts which may be used in the process of the present inven- Patentied July 1969 tion are hydrochlorides of organic amines and zinc nitrate and a mixture thereof.
The baking may be carried out under customary resin treatment conditions. For example, it may be carried out at 120 to 150 C. for 3 to 8 minutes. If the baking is carried out with superheated steam, it is possible to improve further the fastnesses of a heavy color dyeing.
The present invention is illustrated but not limited by the following examples. In the examples fastness to washing was tested according to 118 (Japanese Industrial Standards) L-1045 corresponding to ISO Method MC-2, and fastness to rubbing according to 11$ L-l048 corresponding to AATCC 84961, Crock-meter method, and crease resistance according to I18 L-1003 corresponding to AATCC 664959, Clerks method.
Example 1 A hank of cuprammonium rayon of 75 deniers/54 filaments was immersed for one minute in a treating solution having the following composition:
G./l. A direct black dye Resin treating agent 1 200 Zinc nitrate 5 N-octadecyl-N-ethylene nrea 2 8 1 The resin treating agent was prepared by adding 5% sodium hydroxide to 1.540 cc. of 40% formalin 'to give a pH of S and then adding one kg. of urea thereto and heating the mixture at 80 C. for minutes with stirring and cooling the resultant product.
2 The material is a softener and water repellent. The treated hank was immediately centrifuged and then wrapped in a vinyl chloride sheet. After standing at room temperature for two hours, the hank was dried at 70 C.
A taffeta was woven by employing the above dyed yarn as warp and then baked at 140 C. for four minutes.
Thus a uniformly dyed fabric was obtained having excellent fastnesses and good crease resistance as shown in the following Table 1.
Scoured 100 deniers/ filaments viscose rayon taffeta was padded with a treating solution having the following composition G./l. A direct blue dye 1 1O Resin treating agent 180 Zinc nitrate 5 The padded fabric obtained 72% wet pick-ups and is immediately rolled up and wrapped in a vinyl chloride sheet. After standing at room temperature for two hours, the treated fabric was dried at 80 C. and then baked at 140 C. for five minutes.
The treating agent was prepared by adding 8 cc. of 5 percent sodium hydroxide to 800 cc. of 40 percent formalin to give a pH of 9 and then adding 500 grams of melamine thereto and heating the mixture at 80 C. for 30 minutes and cooling the resultant product.
Thus a uniformly blue dyed fabric was obtained having excellent fastnesses and good crease resistance as shown in the following Table 2.
TABLE 2 Crease Fastncss Fastness resistance, Composition of treating bath to washing to rubbing percent Example 2 4 4 Ex. 2 without resin treating agent. 1 1 30 4 Example 3 Tricot half of 50 deniers/ 38 filaments cuprammonium rayon was padded with a treating solution having the following composition:
G./l. C.I. Direct Red 95 3 Resin treating agent 1 200 Zinc nitrate 5 Silicone emulsion 10 1 The resin treating agent was prepared in the same manner as in Example 1. The fabric is squeezed by a padded mangle to obtain 92 percent mangle expression, and immediately put into a covered box. After standing at room temperature for two hours, the fabric was baked with a pin tenter at 150 C. for five minutes.
Thus a uniformly dyed fabric was obtained having excellent fastnesses and a low shrinkage percentage as shown in following Table 3.
TABLE 3 Washing shrinkage, percent Fastness Fastness to Washing to rubbing Coarse Composition of padding at 1 Well Example 3 5 5 Ex. 3 without resin treating agent 1 1 Example 4 Scoured twill of deniers/33 filaments viscose rayon was padded at 40 C. with a treating solution having the following composition:
G./l. CI. Direct Yellow 50 (CI. 29025) 18 Dimethylethylene urea 70 2-amino-2-methyl-l-propanol hydrochloride 15 Cotton calico which had been previously scoured and bleached by a usual method was at 50 C. padded with a treating solution having the following composition:
G./l. C.I. Direct Black 19 (Cl. 35255) 20 Dimethylol hydroxyethylene urea 60 Trimethoxymethyl melamine 25 2-amino-2-methyl-l-propanol HCl 10 Zinc nitrate 4 Silicone emulsion 8 The padded material obtained 65 percent wet pick-ups, and is immediately allowed to stand in a room having a relative humidity of percent and a temperature of 80 C. for one hour. The fabric was then dried at 70 C. and baked at 140 C. for four minutes. Thus a uniformly dyed fabric was obtained having a good crease resistance and a fastness to washing of grade 5.
Example 6 Scoured viscose rayon staple fiber muslin fabric was padded at room temperature with a treating solution having the following composition:
G./l. Cl. Direct Blue 71 (Cl. 34,140 15 Trimethylolmelamine Zinc nitrate 5 The wet pick-ups of the padded fabric regulated 85% of the dried fabric, and is immediately rolled up and wrapped in a vinyl chloride sheet. After standing at room temperature for 12 hours, the fabric was dried at 70 C. and then baked at 140 C. for four minutes. Thus a uniformly dyed fabric was obtained having a good wet crease resistance and a fastness to washing of grade 5.
Example 7 A cake of 75 deniers/33 filaments viscose rayon was charged into a cake dyeing machine, and a treating solution having the following composition:
G./l. C.I. Direct Black 76 (Cl. 35,865) 6 Dimethylolurea 50 Monomethylolurea 60 Z-amino-Z-methyl-l-propanol hydrochloride 20 N-octadecyl-N-ethylene-urea (a softener) 20 was passed through the inside of the cake at a pressure of meters water with the pump of the dyeing machine for five minutes. Then the cake was dehydrated by a one cake type centrifuge. The Wet pick-ups of the treated cake was 815% of the dried cake, and was immediately wrapped in a vinyl chloride sheet. After standing for three hours at room temperature the cake was dried at 60 C. Twill was woven from thus dyed yarn. The resultant fabric was then baked at 140 C. for four minutes to obtain a uniformly dyed fabric having an excellent crease resistance and good fastnesses.
Example 8 6,000 ends of cuprammonium rayon yarns of 75 deniers/54 filaments which had been warped on a beam, was padded in 80 percent wet pick-up with a treating solution having the following composition:
G./l. C.I. Direct Red 95 c 8 Dimethylol ethylene erea 100 Z-amino-Z-methyl-l-propanol HCl 10 Silicone emulsion 20 Yarns were rewound on another beam, and the padded yarns on the rewound beam were wrapped in a vinyl chloride sheet. After standing at room temperature for two hours, the yarns were dried by passing them through a drying machine. Twill was woven from these yarns as warp and the 75 deniers/ 54 filaments cuprammonium rayon as shown in Example 1 as filling yarns, and the fabric was then baked at 140 C. for five minutes to obtain a uniformly dyed fabric having a good crease resistance and excellent fastnesses.
What we claim is:
1. A process for concurrent dyeing and resin treatment comprising the steps of:
(a) padding cellulosic fibrous materials with an aqueous solution of a direct dye containing an aminoplast precursor treating agent and an acid catalyst and then allowing the padded fiber to stand in a wet state, while suppressing the evaporation of water,
(b) baking the said materials thus treated with either dry heat or superheated steam.
2. A process according to claim 1, wherein said cellulose fiber is selected from the group consisting of viscose rayon, cuprammonium rayon, polynosic rayon, cotton, and hemp fibers.
3. A process according to claim 1 wherein said amino resin treating agent is selected from the group consisting of methylolurea, methylolmelamine, methylol ethylene urea, methylol hydroxyethylene urea, inethylolurone and methyl etherified products thereof and a mixture thereof.
4. A process according to claim 1, wherein said acid catalyst is selected from the group consisting of hydrochlorides of organic amines and zinc nitrate and a mixture thereof.
5. A process according to claim 1 wherein said aqueous solution of a direct color further contains a conventional fiber softener or water repellent.
6. A process according to claim 1 wherein the padded fiber is allowed to stand in a wet state by rolling up and wrapping it in a plastic sheet.
7. A process according to claim 1, wherein the padded fiber is allowed to stand in a wet state by packing it in a covered box.
8. A process according to claim 1, wherein the padded fiber is allowed to stand in a wet state by introducing it into a room of a high humidity.
9. A process according to claim 1 wherein the padded fiber is allowed to stand in a wet state at ordinary temperature for 1 to 3 hours.
10. A process according to claim 1 wherein the padded fiber is allowed to stand in a wet state at to C. for a period of time shorter than one hour.
11. A process according to claim 1 wherein said baking is effected at a temperature of to C. for 3 to 8 minutes.
References Cited UNITED STATES PATENTS 3,177,214 4/1965 Sulzer et a1 8-l8 XR DONALD LEVY, Primary Examiner US. Cl. X.R.
Claims (1)
1. A PROCESS FOR CONCURRENT DYEING AND RESIN TREATMENT COMPRISING THE STEPS OF: (A) PADDING CELLULOSIC FIBROUS MATERIALS WITH AN AQUEOUS SOLUTION OF A DIRECT DYE CONTAINING AN AMINOPLAST PRECURSOR TREATING AGENT AND AN ACID CATALYST AND THEN ALLOWING THE PADDED FIBER TO STAND IN A WET STATE, WHILE SUPPRESSING THE EVAPORATION OF WATER, (B) BAKING THE SAID MATERIALS THUS TREATED WITH EITHER DRY HEAT OR SUPERHEATED STEAM.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60373366A | 1966-12-22 | 1966-12-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3458271A true US3458271A (en) | 1969-07-29 |
Family
ID=24416691
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US603733A Expired - Lifetime US3458271A (en) | 1966-12-22 | 1966-12-22 | Simultaneous aminoplast impregnation and direct dyeing by the pad dwell process followed by hot curing of the aminoplast |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3458271A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4077764A (en) * | 1975-05-28 | 1978-03-07 | Hoechst Aktiengesellschaft | Process for the continuous dyeing of textile polyamide fiber material with metal complex dyes |
| US4288226A (en) * | 1978-11-08 | 1981-09-08 | Ciba-Geigy Corporation | Process for slop-padding textile cellulose material |
| US4290767A (en) * | 1978-09-29 | 1981-09-22 | Ciba-Geigy Corporation | Process for slop-padding textile cellulose material |
| JPS6297990A (en) * | 1986-10-27 | 1987-05-07 | 株式会社日本触媒 | Fluorescent colorant for raw liquid dyed viscose rayon |
| US6040005A (en) * | 1995-08-12 | 2000-03-21 | Zeneca Limited | Colored polymers |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3177214A (en) * | 1959-07-13 | 1965-04-06 | Ciba Ltd | Resinous triazinylamino anthra-quinone dyestuffs |
-
1966
- 1966-12-22 US US603733A patent/US3458271A/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3177214A (en) * | 1959-07-13 | 1965-04-06 | Ciba Ltd | Resinous triazinylamino anthra-quinone dyestuffs |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4077764A (en) * | 1975-05-28 | 1978-03-07 | Hoechst Aktiengesellschaft | Process for the continuous dyeing of textile polyamide fiber material with metal complex dyes |
| US4290767A (en) * | 1978-09-29 | 1981-09-22 | Ciba-Geigy Corporation | Process for slop-padding textile cellulose material |
| US4288226A (en) * | 1978-11-08 | 1981-09-08 | Ciba-Geigy Corporation | Process for slop-padding textile cellulose material |
| JPS6297990A (en) * | 1986-10-27 | 1987-05-07 | 株式会社日本触媒 | Fluorescent colorant for raw liquid dyed viscose rayon |
| US6040005A (en) * | 1995-08-12 | 2000-03-21 | Zeneca Limited | Colored polymers |
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