US2952892A - Cellulosic fabric finishing - Google Patents
Cellulosic fabric finishing Download PDFInfo
- Publication number
- US2952892A US2952892A US598751A US59875156A US2952892A US 2952892 A US2952892 A US 2952892A US 598751 A US598751 A US 598751A US 59875156 A US59875156 A US 59875156A US 2952892 A US2952892 A US 2952892A
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- United States
- Prior art keywords
- fabric
- dispersion
- silicone resin
- acrylic ester
- resins
- 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
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- 239000000675 fabric finishing Substances 0.000 title description 3
- 238000009962 finishing (textile) Methods 0.000 title description 3
- 239000004744 fabric Substances 0.000 claims description 81
- 229920002050 silicone resin Polymers 0.000 claims description 30
- 239000006185 dispersion Substances 0.000 claims description 27
- 239000000839 emulsion Substances 0.000 claims description 16
- 238000001035 drying Methods 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 12
- 150000002148 esters Chemical class 0.000 claims 1
- -1 acrylic ester Chemical class 0.000 description 25
- 229920005989 resin Polymers 0.000 description 17
- 239000011347 resin Substances 0.000 description 17
- 238000011282 treatment Methods 0.000 description 14
- 239000000460 chlorine Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 10
- 229910052801 chlorine Inorganic materials 0.000 description 10
- 241000219146 Gossypium Species 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 229920000742 Cotton Polymers 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 238000004855 creaseproofing Methods 0.000 description 7
- 230000014759 maintenance of location Effects 0.000 description 7
- 239000004753 textile Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 229920001296 polysiloxane Polymers 0.000 description 6
- 230000002411 adverse Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000005299 abrasion Methods 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- WVJOGYWFVNTSAU-UHFFFAOYSA-N dimethylol ethylene urea Chemical compound OCN1CCN(CO)C1=O WVJOGYWFVNTSAU-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 229920000297 Rayon Polymers 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 238000004900 laundering Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- 238000004383 yellowing Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000010409 ironing Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 2
- MOWXJLUYGFNTAL-DEOSSOPVSA-N (s)-[2-chloro-4-fluoro-5-(7-morpholin-4-ylquinazolin-4-yl)phenyl]-(6-methoxypyridazin-3-yl)methanol Chemical compound N1=NC(OC)=CC=C1[C@@H](O)C1=CC(C=2C3=CC=C(C=C3N=CN=2)N2CCOCC2)=C(F)C=C1Cl MOWXJLUYGFNTAL-DEOSSOPVSA-N 0.000 description 1
- 241000256844 Apis mellifera Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 125000005474 octanoate group Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- 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
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2369—Coating or impregnation improves elasticity, bendability, resiliency, flexibility, or shape retention of the fabric
- Y10T442/2393—Coating or impregnation provides crease-resistance or wash and wear characteristics
Definitions
- This invention relates to textile fabric finishing and is especially concerned with the treatment of cellulosic fabrics, such as cotton, rayon and linen.
- a treatment which not only imparts a high degree of crease resistance but completely eliminates chlorine retention.
- This is accomplished, by the present invention, by the employment in combination of two resins, i.e., a polymerized acrylic ester and a silicone resin.
- a polymerized acrylic ester i.e., a polymerized acrylic ester and a silicone resin.
- these two resins contains nitrogen annd therefore neither of them is capable of chlorine retention as descrlbed above.
- neither of these resins used alone is known that this type imparts water repellency, this type of resin has not been used for imparting crease resistance.
- the fabric treated according to the present invention further shows some increase in crease resistance as a result of at least the initial home launderings. As will further appear, especially advantageous results are secured when employing the two resins in certain quantities or ratios hereinafter set forth.
- either of the well known general types of compressive shrinkage machines may be used, i.e., the Palmer type of machine or the rubber blanket type of machine in each of which the drying drums, rolls or other elements may serve to impart sufficient heat to the impregnated and shrunk fabric to fix the finish effect.
- cot-- ton fabric for example 136/60 3.60 yards per lb. broadcloth is dipped in a dispersion comprising an aqueous emulsion of a polymerized acrylic ester and a silicone resin.
- the fabric is squeezed sufiiciently to leave a pick-up of from 65% to of the dispersion by Weight on the fabric.
- the fabric is dried to eliminate water, the drying preferably being suflicient to reduce the water to a value below 10 or 15% of the weight of the fabric. This drying may, if desired, be continued sufficiently to render the fabric bone dry.
- the fabric web is then passed through a compressive shrinkage machine, for instance, a Palmer type machine with the pressure shoe and feed adjusted to impart the desired degree of shrinkage.
- a compressive shrinkage machine for instance, a Palmer type machine with the pressure shoe and feed adjusted to impart the desired degree of shrinkage.
- the drying drum of the Palmer machine is heated sufiiciently to heat the fabric to a temperature between about 200 and 260 F,
- Acrylic esters of the type here contemplated for use are water insoluble thermoplastics and are also characterized by ability to form somewhat rubbery films.
- the silicone resins which are useable according to the invention are polymeric silicone materials having labile hydrogen atoms attached thereto. These silicone resins may be termed methyl hydrogen polysilox-anes and the resin materials which are useable according to the invention comprise aqueous emulsions of such polysiloxanes, constituting oily liquids, which on heating in thin layers yield infusible non-tacky, flexible films. These materials are available in polymerized but relatively low molecular weight form, for instance, a molecular weight of about 1,000 having a viscosity of the order of 1000 to 100,000 centistokes.
- silicone resins here contemplated for use are also water insoluble and are thermosetting to an infusible state under the conditions of heat treating of the impregnated fabric contemplated according to the invention.
- This general class of silicone resins are also known as textile silicone resins and have heretofore been used in the water proofing of textile fabrics.
- the resins are advantageous to use in the form of an aqueous emulsion.
- the water of the emulsion may or may not contain certain other ingredients in solution therein as will be brought out more fully hereinafter.
- the resins could be applied to the fabric in solution in some organic solvent this technique is not as economically feasible, especially in View of the great simplicity of applying such materials in an aqueous medium. 7
- the quantity of the acrylic ester present in the impregnating dispersion should be between .5% and by weight and the quantity of the silicone resin should be between .4% and 4% by weight. Especially good results are obtainable where the acrylic ester is used from 1.2% to 3% and where the silicone is used from .5% to 1.25%. Preferably the quantity of the acrylic ester should be from 1.5 to 2.5 times the quantity of the silicone resin by weight. With a pick-up of from 65% to 75% of the dispersion on the fabric, this would provide from 325% to 3.75% of the acrylic ester and from .26% to 3% of the silicone resin on the fabric by weight.
- the dispersion preferably also contains some stabilizing agent for the emulsion, for instance, an alkyl aryl polyether alcohol, an example of which is available to the trade under the trademark Triton X-155, marketed by Rohm & Haas Co.
- a catalyst for the silicone resin constituent may also be present in the dispersion for instance sodium bicarbonate, sodium aluminate, or a metallic salt of a carboxy acid, such asthe acetates, hexoates, octoates and naphthenates of lead, iron, zinc, manganese or cobalt, an example of which is available to the market under, the trademark Cobelfix marketed by Arkansas Chemical Company.
- the presence of either 1h? $94 11 sion stabilizing agent or the catalyst is not essential to the practice of the invention.
- the dispersion may be applied to the fabric either by dipping the fabric or by padding, or by any other convenient technique.
- the temperature of such heat treatment may range from 200 F. to 350 F. from a time ranging from 5 minutes to aboutlO seconds.
- the temperature of such heat treatment may range from 200 F. to 350 F. from a time ranging from 5 minutes to aboutlO seconds.
- a temperature within this latter range may readily be attained during the passage 'of the fabric through a compressive shrinkage machine, as is contemplated.
- Even relatively short times within this lower temperature range for instance, a time from about 10 seconds to about 60 seconds is sufiicient to effectively fix the finish and provide good durability.
- Example I was impregnated with an aqueous dispersion containing the following:
- the impregnated fabric was squeezed to yield a dispersion pick-up of 65% over and above the dry weight of the fabric, and was then frame dried.
- the finished fabric had increased abrasion resistance, high crease resistance, a pleasing hand and did not lose any strength when subjected to a chlorine rinse, water rinse, drying and heating with an iron for 30 seconds at 350 F., according to the Tentative Test Method 69-52 of the 1955 Technical Manual and Year Book of the AATCC.
- a similar piece of fabric which was treated with 2' /2% dimethylolethyleneurea lost over 55% of its strength when tested in the same manner.
- the fabric treated with dimethylolethyleneurea also had considerably lower abrasion resistance.
- Example 11 Example 111 A pure bleached cotton poplin fabric, 102/48, was handled as in Example II. After the drying but before passage through the compressive shrinkage machine, the crease resistance of the fabric was moderately increased. After being subjected to the heating in passing through the compressive shrinkage machine the crease resistance was extensively increased-90% greater than thesame untreated fabric.
- Example IV A pure bleached cotton poplin, 102/48, was handled as in Example III, except that the quantity of the silicone resin was reduced to .4% of the dispersion. This resulted in slightly less crease resistance than in Example III, but it still approximated 85% over the untreated fabric.
- Example V A pure bleached cotton print fabric, 80/80, 4.00 yds./ 1b., was handled as in Example III, except that the quantity of the silicone resin was increased to 2.88% of the dispersion. This also resulted in comparable increase in crease resistance. Tests further show that the concentration of the silicon resin can be further increased to about 4% of the dispersion without appreciable adverse influence on the desired combination of properties of the treated fabric, but such further increase in the concentration ordinarily does not further increase the crease resistance.
- Example X the same fabric as in Example H was treated in the same way as in that example, except that for the silicone resin (Hydro-Pruf) a similar silicone, Decetex 104, made by Dow-Corning Co. was used. The results were essentially the same.
- Example XI In this example, the same fabric as in Example 11 was treated in the same way as in that example, except that for the acrylic ester (Rhoplex B-15) a similar acrylic, Rhoplex S-1, made by Rohm & Haas Co., was used. The results again were essentially the same.
- the acrylic ester Rhoplex B-15
- Rhoplex S-1 made by Rohm & Haas Co.
- Example XII In this example the fabric and treatment conditions were the same as for Example VII, except that the dispersion contained no emulsion stabilizer and no catalyst. This resulted in a 30% increase in crease resistance, as compared with 42% for Example VII.
- Example XIII This example illustrates the application of the treatment to a linen fabric.
- An all linen fabric, 42/34, 2.5 yds./lb. was treated with a dispersion according to the 6 formulation in Example I. After drying the fabric the crease resistance was increased 21%.
- Example XIV This example illustrates the application of the treatment to a rayon fabric.
- a regenerated cellulose rayon 34/32, 1.82 yds./lb. was treated with the dispersion according to Example I. After drying the fabric, the crease resistance was 29% above the untreated fabric.
- a method for treating cellulosic fabrics to impart durable crease resistance thereto comprises impregnating the fabric with a dispersion comprising an aqueous emulsion of a polymerized acrylic ester and of a silicone resin, said acrylic ester comprising from .5% to 5% by weight of the dispersion and said silicone resin comprising from .4% to 4% of the dispersion, and thereafter drying the impregnated fabric.
- a method for treating cellulosic fabrics to impart durable crease resistance thereto comprises impregnating the fabric with a dispersion comprising an aqueous emulsion of a polymerized acrylic ester and of a silicone resin, said acrylic ester comprising from .5% to 5% by weight of the dispersion and said silicone resin comprising from .4% to 4% of the dispersion, drying the impregnated fabric to a moisture content below 15%, and thereafter heating the fabric to a temperature of from 200 F. to 350 F. for a time from 5 minutes to 10 seconds.
- a textile fabric impregnating composition for use in crease-proofing cellulosic fabrics comprising an aqueous emulsion of fiom .5 to 5% by weight of a polymerized acrylic ester and from .4% to 4% of a silicone resin, the quantity of acrylic ester being from 1.5 to 2.5 times by weight of the quantity of the silicone resin.
- a cellulosic textile fabric carrying a crease-proofing agent comprising, by weight of the fabric, a mixture of from 325% to 3.75% of a polymerized acrylic ester and from 26% to 3% of a silicone resin, the quantity of the acrylic ester being from 1.5 to 2.5 times the quantity of the silicone resin by weight.
- a process for crease-proofing cellulosic textile fabrics by applying an impregnant to the fabric characterized in that the impregnant applied to the fabric comprises an aqueous emulsion of a mixture of a polymerized acrylic ester and a silicone resin, the quantity of the acrylic ester being from 1.5 to 2.5 times the quantity of the silicone resin by weight.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
CELLULOSIC FABRIC FINISHING Charles D. Stump, Wilmington, Del., assignor to Joseph Bancroft & Sons Company, Rockford, Wilmington, Del., a corporation of Delaware No Drawing. Filed July 19, 1956, Ser. No. 598,751
7 Claims. (Cl. 28-74) This invention relates to textile fabric finishing and is especially concerned with the treatment of cellulosic fabrics, such as cotton, rayon and linen.
It has long been known that various altered characteristics may be imparted to fabrics by processes for treatment with resins or resin-like materials, the effect of many of such treatments being. rendered durable, i.e., resistant to laundering and cleaning, by curing or heat treating the resin impregnated fabric. In this Way altered characteristics, such as increased crease resistance, increased water repellency and the like may be imparted to various fabrics.
-As is also known, various of these treatments, while imparting certain desired characteristics to the fabric also have a tendency to adversely influence certain other characteristics in a manner which is disadvantageous for some uses for which the fabrics are intended. This is especially true with respect to known treatments for imparting good crease resistance to cellulosic fabrics, for instance, cotton fabrics intended for use as shirting material or cotton fabrics intended for use as bed sheets, or nurses or barbers uniforms.
In a typical case of a cotton fabric intended for use as a shirting material, the known treatments for crease proofing, for instance, the employment of urea formaldehyde or melamine resins, while imparting substantial crease resistance, at the same time, adversely influence the fabric in certain other respects, notably with respect to what is termed chlorine retention. In further explanation of this adverse influence, it is noted that the common types of resins employed for crease proofing contain amino groups or nitrogen which rather readily react with chlorine commonly present in bleaching agents used in laundering such fabrics. Such bleaching sometimes directly results in yellowing and loss of strength of the fabric. Moreover, in many cases where imme diate yellowing or loss of strength does not occur, these adverse influences occur when the bleached fabric is subsequently heated, for instance, by ironing, the heat of the ironing tending to cause split-off of hydrochloric acid which attacks the cellulose of the fabric and causes undesired yellowing and also weakening of the fabric.
This undesirable chlorine retention has long been recognized as a disadvantage of various known crease proofing treatments, and various attempts have been made to diminish chlorine retention. Some improvement in this direction is achieved by the use of dimethylolethyleneurea as the impregnant for the fabric, the improvement apparently being due to the fact that in the molecule of the dimethylolethyleneurea the nitrogen is in part blocked so that linkage with chlorine is reduced.
According to the present invention, a treatment is provided which not only imparts a high degree of crease resistance but completely eliminates chlorine retention. This is accomplished, by the present invention, by the employment in combination of two resins, i.e., a polymerized acrylic ester and a silicone resin. Neither of States Patent ice these two resins contains nitrogen annd therefore neither of them is capable of chlorine retention as descrlbed above. However, neither of these resins used alone is known that this type imparts water repellency, this type of resin has not been used for imparting crease resistance. If an attempt be made to increase the quantity of the silicone resin (used alone) in an effort to impart some appreciable degree of crease resistance the water repellency of the fabric is exaggerated to a degree which is undesirable for many fabric uses such for example as for shirting material. In addition, the silicone resin is an expensive ingredient and use of excessive quantities is uneconomical.
I have found, however, that by using the acrylic ester and the silicone resin together, a highly desirable balance of fabric characteristics is achieved including high crease resistance, water absorbency, good hand, high abrasion.
resistance, and no chlorine retention. In addition to this desirable combination of properties, the fabric treated according to the present invention further shows some increase in crease resistance as a result of at least the initial home launderings. As will further appear, especially advantageous results are secured when employing the two resins in certain quantities or ratios hereinafter set forth.
Beyond the foregoing, I have further found that by the employment of the combination of resins referred to the heating treatment of the impregnated fabric to fix the finish effect may be accomplished in a shorter time and/ or at a lower temperature than has been required for various of the prior art crease proofing impregnants. In view of this it is feasible, and the invention contemplates as preferred practice, to use a known type of compressive shrinkage machine for effecting the heat treatment. Thus, with a cotton shirting fabric, the invention contemplates both shrinkage and heat treatment in the same operation, i.e., during the passage of the fabric web through the compressive shrinkage machine. For this purpose either of the well known general types of compressive shrinkage machines may be used, i.e., the Palmer type of machine or the rubber blanket type of machine in each of which the drying drums, rolls or other elements may serve to impart sufficient heat to the impregnated and shrunk fabric to fix the finish effect.
In a typical treatment according to the invention, cot-- ton fabric, for example 136/60 3.60 yards per lb. broadcloth is dipped in a dispersion comprising an aqueous emulsion of a polymerized acrylic ester and a silicone resin. After the dipping, the fabric is squeezed sufiiciently to leave a pick-up of from 65% to of the dispersion by Weight on the fabric. Thereafter, the fabric is dried to eliminate water, the drying preferably being suflicient to reduce the water to a value below 10 or 15% of the weight of the fabric. This drying may, if desired, be continued sufficiently to render the fabric bone dry. The fabric web is then passed through a compressive shrinkage machine, for instance, a Palmer type machine with the pressure shoe and feed adjusted to impart the desired degree of shrinkage. The drying drum of the Palmer machine is heated sufiiciently to heat the fabric to a temperature between about 200 and 260 F,
polymers may also be used provided the secondary con stituents are present only in very small quantities, as it is desired to employ a so called soft or textile type of acrylic ester, in order to avoid impairing the hand of the fabric. Acrylic esters of the type here contemplated for use are water insoluble thermoplastics and are also characterized by ability to form somewhat rubbery films.
The silicone resins which are useable according to the invention are polymeric silicone materials having labile hydrogen atoms attached thereto. These silicone resins may be termed methyl hydrogen polysilox-anes and the resin materials which are useable according to the invention comprise aqueous emulsions of such polysiloxanes, constituting oily liquids, which on heating in thin layers yield infusible non-tacky, flexible films. These materials are available in polymerized but relatively low molecular weight form, for instance, a molecular weight of about 1,000 having a viscosity of the order of 1000 to 100,000 centistokes. The silicone resins here contemplated for use are also water insoluble and are thermosetting to an infusible state under the conditions of heat treating of the impregnated fabric contemplated according to the invention. This general class of silicone resins are also known as textile silicone resins and have heretofore been used in the water proofing of textile fabrics.
Because of the physical characteristics of both of the types of resins described, it is advantageous to use the resins in the form of an aqueous emulsion. The water of the emulsion may or may not contain certain other ingredients in solution therein as will be brought out more fully hereinafter. Although the resins could be applied to the fabric in solution in some organic solvent this technique is not as economically feasible, especially in View of the great simplicity of applying such materials in an aqueous medium. 7
In preparing the impregnant for application to the fabric, it is convenient to merely intermix aqueous emulsions of the two resin constituents, for instance, the com: mercially available emulsion form of these resins and then add whatever water is necessary to provide the desired concentration of resins in the dispersion.
The quantity of the acrylic ester present in the impregnating dispersion should be between .5% and by weight and the quantity of the silicone resin should be between .4% and 4% by weight. Especially good results are obtainable where the acrylic ester is used from 1.2% to 3% and where the silicone is used from .5% to 1.25%. Preferably the quantity of the acrylic ester should be from 1.5 to 2.5 times the quantity of the silicone resin by weight. With a pick-up of from 65% to 75% of the dispersion on the fabric, this would provide from 325% to 3.75% of the acrylic ester and from .26% to 3% of the silicone resin on the fabric by weight.
The dispersion preferably also contains some stabilizing agent for the emulsion, for instance, an alkyl aryl polyether alcohol, an example of which is available to the trade under the trademark Triton X-155, marketed by Rohm & Haas Co. A catalyst for the silicone resin constituent may also be present in the dispersion for instance sodium bicarbonate, sodium aluminate, or a metallic salt of a carboxy acid, such asthe acetates, hexoates, octoates and naphthenates of lead, iron, zinc, manganese or cobalt, an example of which is available to the market under, the trademark Cobelfix marketed by Arkansas Chemical Company. The presence of either 1h? $94 11 sion stabilizing agent or the catalyst is not essential to the practice of the invention.
The dispersion may be applied to the fabric either by dipping the fabric or by padding, or by any other convenient technique.
Although some improvement in crease resistance is obtainable merely by impregnating the fabric and then subjecting it to low temperature drying to remove the 7 applied moisture, it is preferred to employ at least some heat treatment after the drying. The temperature of such heat treatment may range from 200 F. to 350 F. from a time ranging from 5 minutes to aboutlO seconds. However, since the higher temperatures of'this range are not necessary, it is contemplated to utilize a lower range extending from 200 F. to 260 F. A temperature within this latter range may readily be attained during the passage 'of the fabric through a compressive shrinkage machine, as is contemplated. Even relatively short times within this lower temperature range, for instance, a time from about 10 seconds to about 60 seconds is sufiicient to effectively fix the finish and provide good durability.
In the following examples percentages are given on the weight basis unless otherwise indicated.
Example I was impregnated with an aqueous dispersion containing the following:
1.77% acrylic ester (Rhoplex B-15 emulsion, 46%
made by Rohm & Haas Co.)
0.72% polysiloxane (Hydro-Pruf emulsion,
made by Arkansas Chemical Co.)
0.60% catalyst (Cobelfix, made by Arkansas Chemical 0.96% emulsion stabilizer (Triton X-15-5, made by Rohm & Haas Co.)
The impregnated fabric was squeezed to yield a dispersion pick-up of 65% over and above the dry weight of the fabric, and was then frame dried.
The finished fabric had increased abrasion resistance, high crease resistance, a pleasing hand and did not lose any strength when subjected to a chlorine rinse, water rinse, drying and heating with an iron for 30 seconds at 350 F., according to the Tentative Test Method 69-52 of the 1955 Technical Manual and Year Book of the AATCC. A similar piece of fabric which was treated with 2' /2% dimethylolethyleneurea lost over 55% of its strength when tested in the same manner. The fabric treated with dimethylolethyleneurea also had considerably lower abrasion resistance.
30% solids,
Example 11 Example 111 A pure bleached cotton poplin fabric, 102/48, was handled as in Example II. After the drying but before passage through the compressive shrinkage machine, the crease resistance of the fabric was moderately increased. After being subjected to the heating in passing through the compressive shrinkage machine the crease resistance was extensively increased-90% greater than thesame untreated fabric.
solids, 7
The abrasion resistance Example IV A pure bleached cotton poplin, 102/48, was handled as in Example III, except that the quantity of the silicone resin was reduced to .4% of the dispersion. This resulted in slightly less crease resistance than in Example III, but it still approximated 85% over the untreated fabric.
Example V A pure bleached cotton print fabric, 80/80, 4.00 yds./ 1b., was handled as in Example III, except that the quantity of the silicone resin was increased to 2.88% of the dispersion. This also resulted in comparable increase in crease resistance. Tests further show that the concentration of the silicon resin can be further increased to about 4% of the dispersion without appreciable adverse influence on the desired combination of properties of the treated fabric, but such further increase in the concentration ordinarily does not further increase the crease resistance.
Examples VI, VII VIII and IX VI VII VIII IX Percent Percent Percent Percent Increase in crease resistance was shown by all of these examples as compared with the untreated in accordance with the following:
VI VII VIII IX Percent Percent Percent Percent 20 42 20 17 Example X In this example, the same fabric as in Example H was treated in the same way as in that example, except that for the silicone resin (Hydro-Pruf) a similar silicone, Decetex 104, made by Dow-Corning Co. was used. The results were essentially the same.
Example XI In this example, the same fabric as in Example 11 was treated in the same way as in that example, except that for the acrylic ester (Rhoplex B-15) a similar acrylic, Rhoplex S-1, made by Rohm & Haas Co., was used. The results again were essentially the same.
Example XII In this example the fabric and treatment conditions were the same as for Example VII, except that the dispersion contained no emulsion stabilizer and no catalyst. This resulted in a 30% increase in crease resistance, as compared with 42% for Example VII.
Example XIII This example illustrates the application of the treatment to a linen fabric. An all linen fabric, 42/34, 2.5 yds./lb. was treated with a dispersion according to the 6 formulation in Example I. After drying the fabric the crease resistance was increased 21%.
Example XIV This example illustrates the application of the treatment to a rayon fabric. Here a regenerated cellulose rayon 34/32, 1.82 yds./lb. was treated with the dispersion according to Example I. After drying the fabric, the crease resistance was 29% above the untreated fabric.
From the above examples, it will be noted that the effect of the treatment varies somewhat with different fabrics. In all cases, the increase in crease resistance is good and in no case was there any indication of chlorine retention.
I claim:
1. A method for treating cellulosic fabrics to impart durable crease resistance thereto, which method comprises impregnating the fabric with a dispersion comprising an aqueous emulsion of a polymerized acrylic ester and of a silicone resin, said acrylic ester comprising from .5% to 5% by weight of the dispersion and said silicone resin comprising from .4% to 4% of the dispersion, and thereafter drying the impregnated fabric.
2. A method according to claim 1 in which the quantity of acrylic ester is from 1.2% to 3% and in which the quantity of silicone is from .5 to 1.25%
3. A method according to claim 1 in which the quantity of acrylic ester in the dispersion is from 1.5 to 2.5 times by weight the quantity of the silicone resin in the dispersion.
4. A method for treating cellulosic fabrics to impart durable crease resistance thereto, which method comprises impregnating the fabric with a dispersion comprising an aqueous emulsion of a polymerized acrylic ester and of a silicone resin, said acrylic ester comprising from .5% to 5% by weight of the dispersion and said silicone resin comprising from .4% to 4% of the dispersion, drying the impregnated fabric to a moisture content below 15%, and thereafter heating the fabric to a temperature of from 200 F. to 350 F. for a time from 5 minutes to 10 seconds.
5. A textile fabric impregnating composition for use in crease-proofing cellulosic fabrics, said composition comprising an aqueous emulsion of fiom .5 to 5% by weight of a polymerized acrylic ester and from .4% to 4% of a silicone resin, the quantity of acrylic ester being from 1.5 to 2.5 times by weight of the quantity of the silicone resin.
6. A cellulosic textile fabric carrying a crease-proofing agent comprising, by weight of the fabric, a mixture of from 325% to 3.75% of a polymerized acrylic ester and from 26% to 3% of a silicone resin, the quantity of the acrylic ester being from 1.5 to 2.5 times the quantity of the silicone resin by weight.
:7. A process for crease-proofing cellulosic textile fabrics by applying an impregnant to the fabric, characterized in that the impregnant applied to the fabric comprises an aqueous emulsion of a mixture of a polymerized acrylic ester and a silicone resin, the quantity of the acrylic ester being from 1.5 to 2.5 times the quantity of the silicone resin by weight.
References Cited in the file of this patent UNITED STATES PATENTS 2,258,220 Rochow Oct. 7, 1941 0,588,365 Dennett Mar. 11, 1952 2,612,482 Rasmussen Sept. 30, 1952 2,768,092 Lawrence Oct. 3. 11956
Claims (1)
1. A METHOD FOR TREATING CELLULOSIC FABRICS TO IMPART DURABLE CREASE RESISTANCE THERETO, WHICH METHOD COMPRISES ILMPREGNATING THE FABRIC WITH A DISPERSION COMPRISING AN AQUEOUS EMULSION OF A POLYMERIZED ACRYLIC ESTER AND OF A SILICONE RESIN, SAID ACRYLIC ESTER COMPRISING FROM .5% TO 5% BY WEIGHT OF THE DISPERSION AND SAID SILICONE RESIN COMPRISING FROM .4% TO 4% OF THE DISPERSION, AND THEREAFTER DRYING THE IMPREGNATED FABRIC.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US598751A US2952892A (en) | 1956-07-19 | 1956-07-19 | Cellulosic fabric finishing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US598751A US2952892A (en) | 1956-07-19 | 1956-07-19 | Cellulosic fabric finishing |
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US2952892A true US2952892A (en) | 1960-09-20 |
Family
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Family Applications (1)
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US598751A Expired - Lifetime US2952892A (en) | 1956-07-19 | 1956-07-19 | Cellulosic fabric finishing |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3844825A (en) * | 1972-11-30 | 1974-10-29 | American Cyanamid Co | Method of producing an acrylic fiber having an improved touch like animal hair |
US6638319B2 (en) | 2001-04-04 | 2003-10-28 | Healthtex Apparel Corp. | Polymer for printed cotton |
US6645255B2 (en) | 2001-04-04 | 2003-11-11 | Healthtex Apparel Corp. | Polymer-grafted stretchable cotton |
US6645256B2 (en) | 2001-04-04 | 2003-11-11 | Healthtex Apparel Corp. | Polymer grafted cotton |
JP2005503492A (en) * | 2001-04-04 | 2005-02-03 | ヘルステックス アパレル コーポレイション | Improved polymer grafted cotton fibers and products |
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US2258220A (en) * | 1940-04-27 | 1941-10-07 | Gen Electric | Resinous materials and insulated conductors and other products utilizing the same |
US2588365A (en) * | 1949-11-10 | 1952-03-11 | Dow Corning | Method of rendering fabrics waterrepellent and product resulting therefrom |
US2612482A (en) * | 1950-03-17 | 1952-09-30 | Gen Electric | Water-repellent compositions |
US2768092A (en) * | 1954-03-24 | 1956-10-23 | Cranston Print Works Co | Method for imparting waved finish to textile fabrics |
-
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- 1956-07-19 US US598751A patent/US2952892A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2258220A (en) * | 1940-04-27 | 1941-10-07 | Gen Electric | Resinous materials and insulated conductors and other products utilizing the same |
US2588365A (en) * | 1949-11-10 | 1952-03-11 | Dow Corning | Method of rendering fabrics waterrepellent and product resulting therefrom |
US2612482A (en) * | 1950-03-17 | 1952-09-30 | Gen Electric | Water-repellent compositions |
US2768092A (en) * | 1954-03-24 | 1956-10-23 | Cranston Print Works Co | Method for imparting waved finish to textile fabrics |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3844825A (en) * | 1972-11-30 | 1974-10-29 | American Cyanamid Co | Method of producing an acrylic fiber having an improved touch like animal hair |
US6638319B2 (en) | 2001-04-04 | 2003-10-28 | Healthtex Apparel Corp. | Polymer for printed cotton |
US6645255B2 (en) | 2001-04-04 | 2003-11-11 | Healthtex Apparel Corp. | Polymer-grafted stretchable cotton |
US6645256B2 (en) | 2001-04-04 | 2003-11-11 | Healthtex Apparel Corp. | Polymer grafted cotton |
US20040072948A1 (en) * | 2001-04-04 | 2004-04-15 | Sanduja Mohan L. | Polymer-grafted stretchable cotton |
JP2005503492A (en) * | 2001-04-04 | 2005-02-03 | ヘルステックス アパレル コーポレイション | Improved polymer grafted cotton fibers and products |
US6908976B2 (en) | 2001-04-04 | 2005-06-21 | Healthtex Apparel Corp. | Polymer-grafted stretchable cotton |
JP4647188B2 (en) * | 2001-04-04 | 2011-03-09 | ヘルステックス アパレル コーポレイション | Improved polymer-grafted cotton fibers and products |
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