US3039167A - Method for improving the properties of fabrics containing cross-linked regenerated cellulose material - Google Patents
Method for improving the properties of fabrics containing cross-linked regenerated cellulose material Download PDFInfo
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- US3039167A US3039167A US837583A US83758359A US3039167A US 3039167 A US3039167 A US 3039167A US 837583 A US837583 A US 837583A US 83758359 A US83758359 A US 83758359A US 3039167 A US3039167 A US 3039167A
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- fabric
- regenerated cellulose
- cross
- linked
- improving
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- 239000004744 fabric Substances 0.000 title claims description 50
- 238000000034 method Methods 0.000 title claims description 15
- 239000004627 regenerated cellulose Substances 0.000 title claims description 15
- 239000000463 material Substances 0.000 title description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 238000005213 imbibition Methods 0.000 claims description 11
- 229920003043 Cellulose fiber Polymers 0.000 claims description 9
- 239000012736 aqueous medium Substances 0.000 claims description 6
- 239000000835 fiber Substances 0.000 description 23
- 206010001497 Agitation Diseases 0.000 description 16
- 238000013019 agitation Methods 0.000 description 16
- 238000011282 treatment Methods 0.000 description 13
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 10
- 239000003431 cross linking reagent Substances 0.000 description 9
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 238000004132 cross linking Methods 0.000 description 7
- 239000000080 wetting agent Substances 0.000 description 7
- 229920002678 cellulose Polymers 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 4
- 239000001913 cellulose Substances 0.000 description 4
- 238000009963 fulling Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000012260 resinous material Substances 0.000 description 4
- 210000002268 wool Anatomy 0.000 description 4
- 235000013877 carbamide Nutrition 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- -1 methylol 1,2-propylene Chemical group 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229920003180 amino resin Polymers 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- WVJOGYWFVNTSAU-UHFFFAOYSA-N dimethylol ethylene urea Chemical compound OCN1CCN(CO)C1=O WVJOGYWFVNTSAU-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical class OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 235000017858 Laurus nobilis Nutrition 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- VGGLHLAESQEWCR-UHFFFAOYSA-N N-(hydroxymethyl)urea Chemical class NC(=O)NCO VGGLHLAESQEWCR-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001744 Polyaldehyde Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 235000005212 Terminalia tomentosa Nutrition 0.000 description 1
- 244000125380 Terminalia tomentosa Species 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- QYXHJMXBZWOTJN-UHFFFAOYSA-N formaldehyde;guanidine Chemical compound O=C.NC(N)=N QYXHJMXBZWOTJN-UHFFFAOYSA-N 0.000 description 1
- XVVGGZUZOITHPH-UHFFFAOYSA-N formaldehyde;prop-2-enal Chemical compound O=C.C=CC=O XVVGGZUZOITHPH-UHFFFAOYSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 229940050906 magnesium chloride hexahydrate Drugs 0.000 description 1
- DHRRIBDTHFBPNG-UHFFFAOYSA-L magnesium dichloride hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[Cl-].[Cl-] DHRRIBDTHFBPNG-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229940063557 methacrylate Drugs 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- GJRKKTVFRGJAFQ-UHFFFAOYSA-N prop-2-en-1-ol;urea Chemical compound NC(N)=O.OCC=C GJRKKTVFRGJAFQ-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- BRMSVEGRHOZCAM-UHFFFAOYSA-M sodium;2-dodecanoyloxyethanesulfonate Chemical compound [Na+].CCCCCCCCCCCC(=O)OCCS([O-])(=O)=O BRMSVEGRHOZCAM-UHFFFAOYSA-M 0.000 description 1
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/01—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with hydrogen, water or heavy water; with hydrides of metals or complexes thereof; with boranes, diboranes, silanes, disilanes, phosphines, diphosphines, stibines, distibines, arsines, or diarsines or complexes thereof
- D06M11/05—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with hydrogen, water or heavy water; with hydrides of metals or complexes thereof; with boranes, diboranes, silanes, disilanes, phosphines, diphosphines, stibines, distibines, arsines, or diarsines or complexes thereof with water, e.g. steam; with heavy water
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
Definitions
- the present invention in a principal aspect, therefore, includes a method for improving the properties of woven and knitted fabrics containing a substantial proportion of regenerated cellulose staple fibers which have been crosslinked while in the form of staple to the extent of reducing their water imbibition to not greater than about 70% which comprises subjecting said fabric to wet agitation.
- the present invention comprises a process for improving the properties of woven and knitted fabrics containing a substantial proportion of regenerated cellulose staple fibers which have been crosslnked in the form of staple to reduce their water imbibition to not greater than about 70% which comprises subjecting said fabric to wet agitation and subsequently treating the fabric with a cross-linking agent.
- the regenerated cellulose fibers present in the fabric which is subjected to wet agitation are fibers which have been crosslinked while in the form of staple, so that their water imbibition 1 is reduced to not more than about 70% and preferably to between about 30 and 50%.
- Fabrics made from such fibers do not degrade under wet agitation, but on the contrary not only retain their strength but, surprisingly, act in a manner somewhat similar to wool, to give a light, soft, full fabric, pleasant to touch and of good appearance without, however, the high degree of shrinkage associated with the fulling of wool fibers.
- Cross-linked is a term commonly in use in the art to refer to cellulosic fibers in which the cellulose chains are joined or linked together in a direction transverse to their axis by some external agent.
- An outstanding effect Water imbibition is a measure of the amount of water which will be taken up by a fiber. Specifically it is defined as the percent by weight of water retained in saturated material after centrifuging a 0.5 gm. sample for 5 minutes at 1000 G, and is expressed as percent of the oven dry weight of the fiber.
- cross-linking is to reduce the water imbibition of the cellulose.
- Typical aminoplasts are urea-formaldehyde, melamiiie-formaldehyde, dicyandiamide-formaldehyde, guanidine-formaldehyde and combinations of these ingredients.
- the term is also used in this application to include the methylol-amino-epihalohydrin compounds described in the copending application of George C. Daul, Serial No. 663,345, filed June 4, 1957, now Patent No. 2,960,484.
- resinous materials which are suitable for use in the present invention are those formed by the reaction of formaldehyde and acrolein as described in United States Patent No. 2,696,477; resins formed by the reaction of acetone and formaldehyde as described, for example, in United States Patents No. 2,504,835 and No. 2,711,971; polyepoxy resins, e.g. polyfunctional compounds having at least two epoxy groups linked through a hydrocarbon, a polyhydric phenol or a polyhydric alcohol group, such as the resins formed from saturated polyglycidyl ethers of polyhydric alcohols as described in United States Patent No. 2,752,269.
- Particularly useful compounds of the last named class are the condensation products of epichlorohydrin with ethylene glycols. It will be understood that the precise resin used is not a part of the present invention and other heat hardenable resins used in the textile industry may be employed as desired.
- reactant type resins may be used. Chief among these are the partially or wholly methylated methylolureas and their lower polymers, methylolethylene urea, methylol 1,2-propylene urea and the methyl esters of these cyclic ureas. Such materials may be applied as described in the copending application of Daul Serial No. 819,465, filed June 10, 1959.
- cross-linking agents include formaldehyde, polyaldehydes and hydroxyaldehydes, which may be applied as described in the copending application of Daul et al., Serial No. 819,465, filed June 10, 1959.
- crosslinking agents are not to be intended to be exhaustive and other agents may be used without departing from the invention, provided that the water imbibition of the cellulosic fiber is reduced to below about 70% and provided that this is accomplished by a reaction with the cellulose molecule and not merely by forming a water impervious coating on the outside of the fibers.
- the aqueous medium may be plain water but preferably includes a wetting agent.
- the nature of the wetting agent is not especially important. Conveniently it can be common soap, i.e. the alkali metal salts of a mixture of long chain fatty acids.
- any of numerous synthetic materials having surface active properties can be used including the sulfates and sulfonates of long chain alcohols, e.g. sodium dodecyl sulfate and sodium dodecyl sulfonate, alkyl aryl sulfonates, e.g. sodium lauryl benzene sulfonate, sulfated and sulfonated amides and their derivatives, e.g.
- Igepon A [H C( CH qCH: CH (CH COOCH CH SO Na] o a sulfated and sulfonated esters, e.g.
- esters of polyglycerol and fatty acids esters of polyglycerol and fatty acids, glycol esters of fatty acids, triethanolamine soaps of fatty acids and quaternary ammonium salts such as the Sapamines, e.g.
- wetting agent employed is obviously dependent on the type of agent and on the other conditions of the treatment. The more active the agent, the higher the temperature and the longer the time of treatment, the less agent need be used. In general the liquid will contain from 0.2 to 4% Wetting agent, by weight.
- the pH of the liquor should not, however, be above about 12 and is normally between about 6 and about 11.
- the temperature of the treatment may also vary greatly depending on the time of treatment and the agent used. Generally it will range from 60 C. to 98 C.
- the time of treatment obviously depends on the other variables discussed above. In general it will range from /2 to 6 hours.
- the amount of liquid which will be used, per pound of fabric will depend on various factors, including the type of process, the composition of the liquor, the nature of the fabric and the effect desired. In a batch process, normally between about and about 20 pounds of liquor, per pound of fabric, will be used.
- a conventional fulling machine of the type ordinarily used for W001 may be employed, or small quantities of fabric may be treated in conventional washing machines.
- the wet agitation may be conducted as a part of a dyeing operation.
- the invention is applicable to various types of fabrics including both knitted and woven goods.
- the fabrics must contain a substantial portion, say above about 50% by wei ht of regenerated cellulose fiber which has been cross-linked while in the form of staple. referably they will contain between about 65 and about 100% by Weight cross-linked regenerated cellulose staple fiber. It is preferred that the fabric not contain regenerated cellulose fiber which is not cross-linked.
- Other fibers which may be used in admixture with cross-linked regenerated cellulose staple fibers include wool, cotton, linen and other natural vegetable and animal fibers, and synthetic fibers including polyester, polyamide, acrylic and cellulose ester fibers. These other fibers may be present in the fabric as an integral part of yarns or threads which also contain cross-linked cellulosic fiber, or they may be present in the fabric as separate yarns or threads not containing cross-linked regenerated cellulose fibers.
- the fabric may be Washed with clear water to remove the additives present in the fulling bath, if additives Were used. It may then be dried and subjected to conventional finishing treatments as desired.
- treatment according to the invention results in a fabric having a full even cover.
- the precise effect obtained may be controlled by varying the degree of cross-linking or the severity of agitation, or both, to give a range of materials extruding from those exhibiting a hard worsted-like effect to those exhibiting a soft woolen-like effect.
- the agent itself has the characteristics described earlier in this specification.
- the fabric is passed through an aqueous solution or dispersion of the crosslinking agent and squeezed to retain between about 70 and about of the agent on the fabric, dried and cured at say to C.
- treated fabrics into garments before impregnating with a crease retaining cross-linking agent.
- treated fabric made in accordance with the invention may be cut and sewn to form a garment and the garment pressed to cure the resin and impart permanent creases.
- Example I Textile grade rayon staple fiber. is impregnated while still in the gel state in accordance with the technique described in Daul et al. Serial No. 635,695, with a liquid containing 5% of an acrolein-formaldehyde precondensate (1 mole of acrolein:4 moles of formaldehyde) 5% of an urea formaldehyde precondensate (1 mole urea: 1.6 moles formaldehyde), 0.75% magnesium chloride hexahydrate (catalyst) and 0.15% of a laurel ketene dimer with 0.05% polyglycol stearate (finishing agents).
- the impregnated fiber is then squeezed to reduce the liquid content to 90% of the weight of the cellulose, dried and cured. It has a water imbibition of 44%.
- the fiber is then made up into yarn, on conventional textile machinery, and a muslin fabric is manufactured therefrom. A piece of this fabric, by 40 inches, in the loom state is put into a home Washing machine with 10 gallons of Water at 160 C. to which 0.2% laundry soap is added. The fabric is agitated in the washing machine for 2 hours. At the end of this time, it is rinsed, dried and pressed. It has a soft feel, a light nap and resembles a piece of flannel.
- Example 11 The fabric processed according to Example I is further impregnated with a solution containing (weight percent):
- Example III Rayon staple fiber is impregnated with a solution having the following composition (weight percent):
- Example IV A piece of the fabric processed in accordance with the process of Example III is impregnated with a solution comprising (percent by weight):
- a method for improving the properties of woven and knitted fabrics containing at least regenerated cellulose fiber which has been chemically cross-linked while in the form of staple to reduce its water imbibition to between about 30% and about 70% which comprises subjecting said fabric to agitation in an aqueous medium at a pH of between about 6 and about 12, at a temperature between about C. and about 98 C., and for a time between about /2 and about 6 hours, and until a full even cover is developed.
- a method for improving the properties of woven and knitted fabrics containing at least 50% regenerated cellulose fibers which have been chemically cross-linked While in the form of staple to reduce their water imbibition to between about 30% and about which comprises agitating said fabric in an aqueous medium at a pH between about 6 and about 12 and at a temperature between about 60 C. and about 98 C. until a full even cover is developed; and subsequently treating said fabric with a cross-linking agent to impart crease resistance thereto.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Patented June 19, 19482 Tie 3,039,167 METHOD FUR ROVING TEE PROPERTIES OF FABRICS CGNTAG CROS-LINKED REGEN- ERATED CELLULQSE MATERIAL Geohh'ey V. Lund, Daphne, Alan, assignor to Courtaulds North America Inc., a corporation of Delaware N Drawing. Filed Sept. 2, 1959, Ser. No. 837,583 Claims. (Cl. 26-19) The present invention relates to a method for improving the properties of fabrics containing substantial quantities of cross-linked regenerated cellulose material.
Fabrics made from regenerated cellulose fibers have been in widespread use for many years and have obtained a high level of public acceptance. In the past, however, the kinds of cloth which it has been possible to make, economically, from such fibers have been limited; and in particular it has been difiicult if not impossible to manufacture economically goods having a full appearance or hand; or having a full, even cover such as is normally associated with wool fabrics which have undergone a light fulling operation.
It has now been discovered that fabrics made from regenerated cellulose staple fibers can be given a full hand and a full, even cover by subjecting them to wet agitation, provided that the cellulose fibers have been cross-linked while in the form of staple to the extent of decreasing their water imbibition to not more than about 70%.
The present invention, in a principal aspect, therefore, includes a method for improving the properties of woven and knitted fabrics containing a substantial proportion of regenerated cellulose staple fibers which have been crosslinked while in the form of staple to the extent of reducing their water imbibition to not greater than about 70% which comprises subjecting said fabric to wet agitation.
It has also been discovered that when such fabric, after having been subjected to wet agitation is further treated with a cross-linking agent, its crease resistance is markedly improved, beyond that which would be obtained if the wet agitation had been omitted.
In a second aspect, the present invention, therefore, comprises a process for improving the properties of woven and knitted fabrics containing a substantial proportion of regenerated cellulose staple fibers which have been crosslnked in the form of staple to reduce their water imbibition to not greater than about 70% which comprises subjecting said fabric to wet agitation and subsequently treating the fabric with a cross-linking agent.
In accordance with the present invention, the regenerated cellulose fibers present in the fabric which is subjected to wet agitation are fibers which have been crosslinked while in the form of staple, so that their water imbibition 1 is reduced to not more than about 70% and preferably to between about 30 and 50%.
Fabrics made from such fibers do not degrade under wet agitation, but on the contrary not only retain their strength but, surprisingly, act in a manner somewhat similar to wool, to give a light, soft, full fabric, pleasant to touch and of good appearance without, however, the high degree of shrinkage associated with the fulling of wool fibers.
Cross-linked is a term commonly in use in the art to refer to cellulosic fibers in which the cellulose chains are joined or linked together in a direction transverse to their axis by some external agent. An outstanding effect Water imbibition is a measure of the amount of water which will be taken up by a fiber. Specifically it is defined as the percent by weight of water retained in saturated material after centrifuging a 0.5 gm. sample for 5 minutes at 1000 G, and is expressed as percent of the oven dry weight of the fiber.
of cross-linking is to reduce the water imbibition of the cellulose.
Various agents have been proposed for cross-linking including heat hardenable resinous materials such as the aminoplasts, i.e. heat hardenable condensation products of compounds having at least two amino hydrogens, with methyl forming compounds. Typical aminoplasts are urea-formaldehyde, melamiiie-formaldehyde, dicyandiamide-formaldehyde, guanidine-formaldehyde and combinations of these ingredients. The term is also used in this application to include the methylol-amino-epihalohydrin compounds described in the copending application of George C. Daul, Serial No. 663,345, filed June 4, 1957, now Patent No. 2,960,484.
Other resinous materials which are suitable for use in the present invention are those formed by the reaction of formaldehyde and acrolein as described in United States Patent No. 2,696,477; resins formed by the reaction of acetone and formaldehyde as described, for example, in United States Patents No. 2,504,835 and No. 2,711,971; polyepoxy resins, e.g. polyfunctional compounds having at least two epoxy groups linked through a hydrocarbon, a polyhydric phenol or a polyhydric alcohol group, such as the resins formed from saturated polyglycidyl ethers of polyhydric alcohols as described in United States Patent No. 2,752,269. Particularly useful compounds of the last named class are the condensation products of epichlorohydrin with ethylene glycols. It will be understood that the precise resin used is not a part of the present invention and other heat hardenable resins used in the textile industry may be employed as desired.
In applying the heat hardenable resinous materials referred to above, it is preferred to use the technique de scribed and claimed in the copending application of G. C. Daul et al., Serial No. 635,695, filed January 23, 1957, now Patent No. 2,902,391.
In place of the heat hardenable resinous materials referred to above, the so-called reactant type resins may be used. Chief among these are the partially or wholly methylated methylolureas and their lower polymers, methylolethylene urea, methylol 1,2-propylene urea and the methyl esters of these cyclic ureas. Such materials may be applied as described in the copending application of Daul Serial No. 819,465, filed June 10, 1959.
Still other cross-linking agents include formaldehyde, polyaldehydes and hydroxyaldehydes, which may be applied as described in the copending application of Daul et al., Serial No. 819,465, filed June 10, 1959.
It should be understood that the above listing of crosslinking agents is not to be intended to be exhaustive and other agents may be used without departing from the invention, provided that the water imbibition of the cellulosic fiber is reduced to below about 70% and provided that this is accomplished by a reaction with the cellulose molecule and not merely by forming a water impervious coating on the outside of the fibers.
In carrying out the wet agitation according to the invention, the aqueous medium may be plain water but preferably includes a wetting agent. The nature of the wetting agent is not especially important. Conveniently it can be common soap, i.e. the alkali metal salts of a mixture of long chain fatty acids. Alternatively, any of numerous synthetic materials having surface active properties can be used including the sulfates and sulfonates of long chain alcohols, e.g. sodium dodecyl sulfate and sodium dodecyl sulfonate, alkyl aryl sulfonates, e.g. sodium lauryl benzene sulfonate, sulfated and sulfonated amides and their derivatives, e.g.
Igepon A [H C( CH qCH: CH (CH COOCH CH SO Na] o a sulfated and sulfonated esters, e.g.
sulfated and sulfonated amines, esters of polyglycerol and fatty acids, glycol esters of fatty acids, triethanolamine soaps of fatty acids and quaternary ammonium salts such as the Sapamines, e.g.
The above list is not intended to be exhaustive, but rather to demonstrate that the type of wetting agent used may vary within wide limits.
The proportion of wetting agent employed is obviously dependent on the type of agent and on the other conditions of the treatment. The more active the agent, the higher the temperature and the longer the time of treatment, the less agent need be used. In general the liquid will contain from 0.2 to 4% Wetting agent, by weight. The pH of the liquor should not, however, be above about 12 and is normally between about 6 and about 11.
The temperature of the treatment may also vary greatly depending on the time of treatment and the agent used. Generally it will range from 60 C. to 98 C.
The time of treatment obviously depends on the other variables discussed above. In general it will range from /2 to 6 hours.
The amount of liquid which will be used, per pound of fabric, will depend on various factors, including the type of process, the composition of the liquor, the nature of the fabric and the effect desired. In a batch process, normally between about and about 20 pounds of liquor, per pound of fabric, will be used.
In carrying out the treatment, a conventional fulling machine of the type ordinarily used for W001 may be employed, or small quantities of fabric may be treated in conventional washing machines. In certain instances the wet agitation may be conducted as a part of a dyeing operation.
The invention is applicable to various types of fabrics including both knitted and woven goods. The fabrics must contain a substantial portion, say above about 50% by wei ht of regenerated cellulose fiber which has been cross-linked while in the form of staple. referably they will contain between about 65 and about 100% by Weight cross-linked regenerated cellulose staple fiber. It is preferred that the fabric not contain regenerated cellulose fiber which is not cross-linked. Other fibers which may be used in admixture with cross-linked regenerated cellulose staple fibers include wool, cotton, linen and other natural vegetable and animal fibers, and synthetic fibers including polyester, polyamide, acrylic and cellulose ester fibers. These other fibers may be present in the fabric as an integral part of yarns or threads which also contain cross-linked cellulosic fiber, or they may be present in the fabric as separate yarns or threads not containing cross-linked regenerated cellulose fibers.
After the wet agitation has been completed, the fabric may be Washed with clear water to remove the additives present in the fulling bath, if additives Were used. It may then be dried and subjected to conventional finishing treatments as desired.
As pointed out above, treatment according to the invention results in a fabric having a full even cover. The precise effect obtained may be controlled by varying the degree of cross-linking or the severity of agitation, or both, to give a range of materials extruding from those exhibiting a hard worsted-like effect to those exhibiting a soft woolen-like effect.
As noted above, special advantages are obtained if, subsequent to the wet agitation treatment, the fabric is given a further cross-linking treatment.
Final cross-linking treatments of the type referred to are conventionally given to impart crease resistance to fabrics. It is found that when the fabric has been subjected to a Wet agitation, in accordance with the present invention, much better crease-resistance can be obtained in the subsequent cross-linking treatment.
The specific conditions under which the cross-linking treatment is carried out will, of course, depend on the nature of the cross-linking agent.
The agent itself has the characteristics described earlier in this specification. Preferably the fabric is passed through an aqueous solution or dispersion of the crosslinking agent and squeezed to retain between about 70 and about of the agent on the fabric, dried and cured at say to C.
In certain cases, it may be desirable to impregnate the fabric with the cross-linking agent, dry at a low (say 60 to 80 C.) temperature and then cure at some later time. This is desirable practice in the case of garments having permanent creases where the fabric must be made into the garment before creases, pleats and the like are put in. By using reactant type resins (see above) and suitable catalysts such delayed curing is possible (see Patent No. 2,846,337).
Again it is possible to make the treated fabrics into garments before impregnating with a crease retaining cross-linking agent. Thus, for example, treated fabric made in accordance with the invention may be cut and sewn to form a garment and the garment pressed to cure the resin and impart permanent creases.
Other variations will readily occur to those skilled in the art.
The invention will be further described with reference to the following specific examples which are given for the purposes of illustration only and are not to be taken as in anyway restricting the invention beyond the scope of the appended claims.
Example I Textile grade rayon staple fiber. is impregnated while still in the gel state in accordance with the technique described in Daul et al. Serial No. 635,695, with a liquid containing 5% of an acrolein-formaldehyde precondensate (1 mole of acrolein:4 moles of formaldehyde) 5% of an urea formaldehyde precondensate (1 mole urea: 1.6 moles formaldehyde), 0.75% magnesium chloride hexahydrate (catalyst) and 0.15% of a laurel ketene dimer with 0.05% polyglycol stearate (finishing agents). The impregnated fiber is then squeezed to reduce the liquid content to 90% of the weight of the cellulose, dried and cured. It has a water imbibition of 44%. The fiber is then made up into yarn, on conventional textile machinery, and a muslin fabric is manufactured therefrom. A piece of this fabric, by 40 inches, in the loom state is put into a home Washing machine with 10 gallons of Water at 160 C. to which 0.2% laundry soap is added. The fabric is agitated in the washing machine for 2 hours. At the end of this time, it is rinsed, dried and pressed. It has a soft feel, a light nap and resembles a piece of flannel.
Example 11 The fabric processed according to Example I is further impregnated with a solution containing (weight percent):
Dimethylol cyclic ethylene urea 12 Polymethyl methacrylate 1.75 MgCl .6H O 1.20 Water 85.05
5 Example III Rayon staple fiber is impregnated with a solution having the following composition (weight percent):
Dimethylol cyclic ethylene urea 12 Folymethyl meth-acrylate 1.75 MgCl .6H O 1.20 Water 85.05
Example IV A piece of the fabric processed in accordance with the process of Example III is impregnated with a solution comprising (percent by weight):
Melamine-formaldehyde 6 1.5 Water Balance The fabric is squeezed to a 89% wet pick up; then dried and cured at 150 C. The fabric has improved crease recovery characteristics compared to a piece of the same fabric similarly treated, but which had not been subjected to wet agitation.
I claim:
1. A method for improving the properties of woven and knitted fabrics containing at least regenerated cellulose fiber which has been chemically cross-linked while in the form of staple to reduce its water imbibition to between about 30% and about 70%, which comprises subjecting said fabric to agitation in an aqueous medium at a pH of between about 6 and about 12, at a temperature between about C. and about 98 C., and for a time between about /2 and about 6 hours, and until a full even cover is developed.
2. The method claimed in claim 1 wherein the aqueous medium contains a wetting agent.
3. A method for improving the properties of woven and knitted fabrics containing at least 50% regenerated cellulose fibers which have been chemically cross-linked While in the form of staple to reduce their water imbibition to between about 30% and about which comprises agitating said fabric in an aqueous medium at a pH between about 6 and about 12 and at a temperature between about 60 C. and about 98 C. until a full even cover is developed; and subsequently treating said fabric with a cross-linking agent to impart crease resistance thereto.
4. The method claimed in claim 3 wherein the aqueous medium contains a Wetting agent.
5. The method claimed in claim 3 wherein the agitation is carried out for from about /2 to about 4 hours.
References Cited in the file of this patent UNITED STATES PATENTS 2,051,389 Nuesslein Aug. 18, 1936 2,327,760 Bestian Aug. 24, 1943 2,685,120 Brant Aug. 3, 1954 2,902,391 Daul Sept. 1, 1959
Claims (1)
1. A METHOD FOR IMPROVING THE PORPERTIES OF WOVEN AND KNITTED FABRICS CONTAINING AT LEAST 50% REGENERATED CELLULOSE FIBER WHICH HAS BEEN CHEMICALLY CROSS-LINKED WHILE IN THE FORM OF STAPLE TO REDUCE ITS WATER IMBIBITION TO BETWEEN ABOUT 30% AND ABOUT 70%, WHICH COMPRISES SUBJECTING SAID FABRIC TO AGITATAION IN A AQUEOUS MEDIUM AT A PH OF BETWEEN ABOUT 6 AND ABOUT 12, ATA A TEMPERATURE BETWEEN ABOUT 60*C. AND ABOUT 98*C., AND FOR A TIME BETWEEN ABOUT 1/2 AND ABOUT 6 HOURS, AND UNTIL A FULL EVEN COVER IS DEVELOPED.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US837583A US3039167A (en) | 1959-09-02 | 1959-09-02 | Method for improving the properties of fabrics containing cross-linked regenerated cellulose material |
| GB30122/60A GB950075A (en) | 1959-09-02 | 1960-09-01 | Improvements in the finishing of fabrics comprising a major part of regenerated cellulose fibre |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US837583A US3039167A (en) | 1959-09-02 | 1959-09-02 | Method for improving the properties of fabrics containing cross-linked regenerated cellulose material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3039167A true US3039167A (en) | 1962-06-19 |
Family
ID=25274878
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US837583A Expired - Lifetime US3039167A (en) | 1959-09-02 | 1959-09-02 | Method for improving the properties of fabrics containing cross-linked regenerated cellulose material |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US3039167A (en) |
| GB (1) | GB950075A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3127732A (en) * | 1961-09-18 | 1964-04-07 | John J Brown | Method for producing bulked, highly stretchable textured cotton yarns |
| US3145132A (en) * | 1961-08-02 | 1964-08-18 | Kendall & Co | Woven stretchable fabrics |
| US3146575A (en) * | 1961-08-14 | 1964-09-01 | Courtaulds Ltd | Bulky composite stretch yarn |
| US3218792A (en) * | 1961-10-02 | 1965-11-23 | Courtaulds Ltd | Cellulosic textile material |
| US3224182A (en) * | 1960-03-23 | 1965-12-21 | Whitecroft Ind Holdings Ltd | Process for production of cross-linked cellulosic yarns |
| US3227511A (en) * | 1961-08-02 | 1966-01-04 | Kendall & Co | Methods of forming woven stretchable fabrics |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH1357464D (en) * | 1964-09-21 | 1900-01-01 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2051389A (en) * | 1932-12-30 | 1936-08-18 | Ig Farbenindustrie Ag | Fulling fabrics |
| US2327760A (en) * | 1940-07-19 | 1943-08-24 | Bestian Herbert | Fibrous materials |
| US2685120A (en) * | 1950-03-24 | 1954-08-03 | Bates Mfg Co | Fabric having contoured decorative surface |
| US2902391A (en) * | 1957-01-23 | 1959-09-01 | Courtaulds Inc | Process for improving the properties of regenerated cellulose fibrous material wherein said material is treated while still in the gel state |
-
1959
- 1959-09-02 US US837583A patent/US3039167A/en not_active Expired - Lifetime
-
1960
- 1960-09-01 GB GB30122/60A patent/GB950075A/en not_active Expired
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2051389A (en) * | 1932-12-30 | 1936-08-18 | Ig Farbenindustrie Ag | Fulling fabrics |
| US2327760A (en) * | 1940-07-19 | 1943-08-24 | Bestian Herbert | Fibrous materials |
| US2685120A (en) * | 1950-03-24 | 1954-08-03 | Bates Mfg Co | Fabric having contoured decorative surface |
| US2902391A (en) * | 1957-01-23 | 1959-09-01 | Courtaulds Inc | Process for improving the properties of regenerated cellulose fibrous material wherein said material is treated while still in the gel state |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3224182A (en) * | 1960-03-23 | 1965-12-21 | Whitecroft Ind Holdings Ltd | Process for production of cross-linked cellulosic yarns |
| US3145132A (en) * | 1961-08-02 | 1964-08-18 | Kendall & Co | Woven stretchable fabrics |
| US3227511A (en) * | 1961-08-02 | 1966-01-04 | Kendall & Co | Methods of forming woven stretchable fabrics |
| US3146575A (en) * | 1961-08-14 | 1964-09-01 | Courtaulds Ltd | Bulky composite stretch yarn |
| US3127732A (en) * | 1961-09-18 | 1964-04-07 | John J Brown | Method for producing bulked, highly stretchable textured cotton yarns |
| US3218792A (en) * | 1961-10-02 | 1965-11-23 | Courtaulds Ltd | Cellulosic textile material |
Also Published As
| Publication number | Publication date |
|---|---|
| GB950075A (en) | 1964-02-19 |
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