US2046885A - Textile material - Google Patents
Textile material Download PDFInfo
- Publication number
- US2046885A US2046885A US759743A US75974334A US2046885A US 2046885 A US2046885 A US 2046885A US 759743 A US759743 A US 759743A US 75974334 A US75974334 A US 75974334A US 2046885 A US2046885 A US 2046885A
- Authority
- US
- United States
- Prior art keywords
- methyl methacrylate
- sizing
- textile materials
- materials
- solution
- 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
- 239000000463 material Substances 0.000 title description 41
- 239000004753 textile Substances 0.000 title description 23
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 26
- 238000004513 sizing Methods 0.000 description 22
- 239000000243 solution Substances 0.000 description 16
- 239000003795 chemical substances by application Substances 0.000 description 15
- 229920000642 polymer Polymers 0.000 description 14
- 239000004744 fabric Substances 0.000 description 13
- -1 alkyl naphthalene sulfonic acid Chemical compound 0.000 description 11
- 239000000839 emulsion Substances 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- 239000007788 liquid Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 229920000742 Cotton Polymers 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 7
- 238000001704 evaporation Methods 0.000 description 6
- 238000004900 laundering Methods 0.000 description 6
- 239000004342 Benzoyl peroxide Substances 0.000 description 5
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 5
- 235000019400 benzoyl peroxide Nutrition 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000002270 dispersing agent Substances 0.000 description 4
- 230000000379 polymerizing effect Effects 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000003490 calendering Methods 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 241000416162 Astragalus gummifer Species 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 229920001615 Tragacanth Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000008149 soap solution Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- UBLAMKHIFZBBSS-UHFFFAOYSA-N 3-Methylbutyl pentanoate Chemical compound CCCCC(=O)OCCC(C)C UBLAMKHIFZBBSS-UHFFFAOYSA-N 0.000 description 1
- 229920002955 Art silk Polymers 0.000 description 1
- 241000206575 Chondrus crispus Species 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 241000206672 Gelidium Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical class C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 150000001253 acrylic acids Chemical class 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000006477 desulfuration reaction Methods 0.000 description 1
- 230000023556 desulfurization Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 108010059642 isinglass Proteins 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052627 muscovite Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000011734 sodium Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 210000002268 wool Anatomy 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
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
- D06M15/267—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof of unsaturated carboxylic esters having amino or quaternary ammonium groups
-
- 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
- Y10T442/2402—Coating or impregnation specified as a size
Definitions
- This invention relates to an improved process for sizing textile materials and more particularly refers to a process for impregnating textiles with a novel class of sizing agents.
- a further object is to size textile material with a class of compounds which improves the appearance and wearing qualities of said materials.
- a still further object is to produce textile materials which are unusually white and pleasing in appearance, and which retain these characteristics throughout numerous launderings without the necessity of additional sizing treatment. Additional objects will become apparent from a consideration of the following description and claims.
- the invention is concerned with the application of methyl methacrylate polymers to textile materials.
- This invention in its preferred embodiment is directed to the passage of textile materials through a solution or emulsion containing small amounts of methyl methacrylate monomers, and/or polymers, with subsequent evaporation of the liquid from such materials in order to impart thereto a protective sizing of methyl methacrylate polymers.
- Example 1 A sample of methyl methacrylate was polymerized by mixing with 0.5% by weight of benzoyl peroxide and heating the mixture at 100 C. for 4 hours. A white amorphous solid was obtained. This polymer was stirred with acetone, in the ratio of 5 parts of the polymer to 95 parts of acetone, until the polymer was compietely dissolved. When the solution was cool it was used to impregnate an 80/60 cotton fabric. The cloth was then run through squeeze rolls to remove excess solution and to insure an even distribution of the resin. The solvent was evaporated and the cloth ironed. An unusually white, glossy finish was obtained. The fabric was much fuller and stiffer than the original. Boiling for one-half hour in 0.5% soap solution had no apparent affect on the finish.
- Example 2 100 parts of methyl methacrylate monomer, containing one part of benzoyl peroxide, as added, with vigorous stirring, to 500 parts of a 2% solution of gum tragacanth containing a suitable dispersing agent, such as the sodium salt of an alkyl naphthalene sulfonic acid.
- a suitable dispersing agent such as the sodium salt of an alkyl naphthalene sulfonic acid.
- the emulsion of the methyl methacrylate monomer obtained in this way was used to impregnate a sample of unfinished cotton voile. After the fabric was thoroughly impregnated, it was squeezed out and then dried in an oven at 100 C. The fabric was rendered stiffer and fuller by the treatment, and the finish was highly resistant to laundering.
- Example 3 The emulsion of methyl methacrylate monomer described in Example 2 was heated at C. for 48 hours. This heating caused the methyl methacrylate to polymerize but did not destroy the emulsion. The result was an emulsion of the polymer. This emulsion was used to size a 48/48 unfinished cotton fabric. The fabric was dried and not calendered. A linen-like effect was obtained, which was resistant to laundering.
- Example 5 An 80/ 60 unfinished cotton fabric was immersed in a 15% solution of sodium hydroxide for 10 minutes. It was then squeezed out and washed thoroughly in anhydrous methyl alcohol. After drying it was treated with a 10%'solution of polymerized methyl methacrylate in acetone, squeezed 2 aoaaaes out and dried. It was then wet out and dried by ironing. An unusually white and somewhat lustrous finish was obtained which was not removed by boiling for one-half hour in 0.5% soap solution.
- Example 6 A skein of gel rayon yarn (made up of filaments which have not been dried after coagulation and desulfurization) was washed in water-free acetone until substantially free of water, then treated with a 5% solution of polymerized methyl methacrylate in acetone. The excess solution was carefully removed by pressing the skein between sheets of absorbent material. The treated fibers were found to have a greater elastic recovery and were stiffer and more wear resistant than the untreated fibers.
- the sizing agent selected in accordance with this invention may be applied to the fibers in unpolymerized, partially polymerized or completely polymerized condition.
- an individual alkyl alkacrylate a mixture of two or more may be selected.
- ethyl methacrylate and/or its higher homologues it is particularly advantageous to incorporate therewith methyl methacrylate.
- Beneficial results may also be obtained by incorporation of esters of higher alpha-alkylacrylic acids.
- the sizing agents previously described may be applied to the textile materials in a variety of ways, and the invention is not to be restricted to any given method of sizing such materials. In general, it is advisable to accomplish this sizing by passing the material to be treated through a dilute suspension or emulsion of the sizing agent. Solutions of these agents may be prepared by utilizing well known organic solvents and mixtures thereof, such as alcohols, esters, ketones, hydrocarbons, etc.
- Aqueous emulsions of the alkyl esters of alpha alkyl substituted acrylic acids may be prepared, for example, by the use of dispersing agents such as alkyl naphthalene sulfonic acids, their sodium salts, alkali metal salts of fatty acids, sodium petroleum sulfonate, sulfonated castor oil and other sulfonated vegetable oils, etc.
- the amount of sizing agent in this solution or emulsion may vary considerably depending upon the particular agent selected, the material to be treated and the degree ofstiifness desired. However, an amount ranging from about 0.5% to about 35% based upon the solution or emulsion, is ordinarily quite sufiicient.
- sizing agent very satisfactory results have been obtained by applying the sizing agent to the textile materials in an unpolymerized condition and causing polymerization to take place thereon.
- This may conveniently be accomplished by incorporating in a sizing solution or emulsion a small quantity of a polymerizing. agent.
- agents are 5 advisably those which are capable of giving oil oxygen such as organic peroxides, ozonides, and in particular benzoyl peroxide.
- the sizing solution or suspension may contain additional materials such as plas- 10 ticizers.
- additional materials such as plas- 10 ticizers.
- a representative few of the many plasticizers which are suitable for use herein are camphor, phthalates such as ethyl-, propyl, isopropyl-, butyl-, isobutyl-, cyclohexyl-, dibutyl-, esters of dibasic acids, etc.
- camphor camphor
- phthalates such as ethyl-, propyl, isopropyl-, butyl-, isobutyl-, cyclohexyl-, dibutyl-, esters of dibasic acids, etc.
- additional plasticizers and combinations thereof as well as additional modifications of other features of the present invention will not be given in detail herein, since one familiar with the art should have no difiiculty in carrying out 20 this invention in accordance with the instructions hereof.
- protective colloids in producing dispersions of methyl methacrylate monomers and related alkyl alkacrylate derivatives is particularly helpful.
- gum tragacanth is well adapted for this purpose.
- the invention is not restricted thereto since other well known protective colloids may be substituted therefor or used in admixture therewith.
- a representative few of these compounds are, for example, casein, gelatin, glue, Russian isinglass, Irish moss, etc.
- Dispersions of, for example, polymeric methyl methacrylate may readily be obtained by dissolving said compound in an organic solvent, adding thereto a suitable dispersing agent, and 40 then adding water under continuous violent agitation.
- dispersions may be obtained in an internal mixer, such as a Bunbury mill, by working the compound to be dispersed with a dispersing agent and a protective colloid, and dilut- 45 ing with water to the desired solids content.
- Textile materials to be sized may be derived from animal, synthetic or vegetable sources.
- the term textile materials" when used herein is understood to include woven, knitted and ma 50 terial otherwise fabricated from fibers, threads, filaments, etc., of silk, artificial silk, cotton, wool, linen, jute, etc.
- After passing the aforementioned or related materials through the sizing bath they may be run through squeeze rolls to 55 remove excess solution and to improve the penetratlon of the solution into the material.
- the solvent or dispersing medium may then be evaporated therefrom, or if a water-soluble solvent is used, the resin may be precipitated on the 60 textile material by immersing said material in water.
- the treated article may be ironed or calendered.
- the disadvantages of prior art sizing agents are overcome 35 to a great extent.
- the process is both speedy and eflicient, and results in a surprisingly white product of pleasing feel and appearance.
- the product possesses exceptional fastness to laundering, and retains its superior characteristics after 7 repeated launderings.
- a process for sizing textile materials which comprises passing said materials through a liquid containing an alkyl alkacrylate and subsequently evaporating the liquid from the treated material.
- a process for sizing textile materials which comprises passing said materials through a liquid containing methyl methacrylate polymers and subsequently evaporating the liquid from the treated material.
- a process for sizing textile materials which comprises passing said materials through a liquid containing methyl methacrylate monomer and a polymerizing agent and subsequently evaporating the liquid from the treated material and polymerizing the methyl methacrylate monomer.
- a process for sizing textile materials which comprises passing said materials through a liquid containing methyl methacrylate monomer and benzoyl peroxide and subsequently evaporating the liquid from the treated material and polymerizing the methyl methacrylate monomer.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
Patented July 7, 1936 UNITED STATES PATENT OFFICE TEXTILE MATERIAL No Drawing. Application December 29, 1934, Serial No. 759,743
9 Claims. (CI. 91-68) This invention relates to an improved process for sizing textile materials and more particularly refers to a process for impregnating textiles with a novel class of sizing agents.
Heretofore textile materials have been sized with starch, gum, tallow, and similar agents. The sized products, however, were not laundry fast and speedily lost their sizing on washing. The product then became limp and lacked body and weight. Likewise, the feel and appearance of the fabrics was far from satisfactory.
It is an object of this invention to overcome the aforementioned defects and numerous other objections which directly or indirectely resulted therefrom. A further object is to size textile material with a class of compounds which improves the appearance and wearing qualities of said materials. A still further object is to produce textile materials which are unusually white and pleasing in appearance, and which retain these characteristics throughout numerous launderings without the necessity of additional sizing treatment. Additional objects will become apparent from a consideration of the following description and claims.
These objects are attained according to the herein described invention wherein textile materials are treated with alkyl alkacrylates in such manner that polymers of said compounds adhere to the fibers. In a more restricted sense the invention is concerned with the application of methyl methacrylate polymers to textile materials. This invention in its preferred embodiment is directed to the passage of textile materials through a solution or emulsion containing small amounts of methyl methacrylate monomers, and/or polymers, with subsequent evaporation of the liquid from such materials in order to impart thereto a protective sizing of methyl methacrylate polymers.
The invention may be more readily understood by a consideration of the following illustrative examples.
Example 1 A sample of methyl methacrylate was polymerized by mixing with 0.5% by weight of benzoyl peroxide and heating the mixture at 100 C. for 4 hours. A white amorphous solid was obtained. This polymer was stirred with acetone, in the ratio of 5 parts of the polymer to 95 parts of acetone, until the polymer was compietely dissolved. When the solution was cool it was used to impregnate an 80/60 cotton fabric. The cloth was then run through squeeze rolls to remove excess solution and to insure an even distribution of the resin. The solvent was evaporated and the cloth ironed. An unusually white, glossy finish was obtained. The fabric was much fuller and stiffer than the original. Boiling for one-half hour in 0.5% soap solution had no apparent affect on the finish.
Example 2 100 parts of methyl methacrylate monomer, containing one part of benzoyl peroxide, as added, with vigorous stirring, to 500 parts of a 2% solution of gum tragacanth containing a suitable dispersing agent, such as the sodium salt of an alkyl naphthalene sulfonic acid. The emulsion of the methyl methacrylate monomer obtained in this way was used to impregnate a sample of unfinished cotton voile. After the fabric was thoroughly impregnated, it was squeezed out and then dried in an oven at 100 C. The fabric was rendered stiffer and fuller by the treatment, and the finish was highly resistant to laundering.
Example 3 The emulsion of methyl methacrylate monomer described in Example 2 was heated at C. for 48 hours. This heating caused the methyl methacrylate to polymerize but did not destroy the emulsion. The result was an emulsion of the polymer. This emulsion was used to size a 48/48 unfinished cotton fabric. The fabric was dried and not calendered. A linen-like effect was obtained, which was resistant to laundering.
Examp e 4 100 parts of methyl methacrylate monomer containing one part of benzoyl peroxide was dissolved in 101 parts of the butyl ether of glycol. This solution was used to impregnate an /60 cotton fabric. After impregnation, the fabricwas heated for 10 minutes at C. A permanent sizing effect was obtained, which, upon calendering with hot rolls, yielded a lustrous, linenlike finish. The glycol butyl ether is a high boiling solvent and tends to retain the methyl methacrylate on the fabric until polymerization occurs. In this mannerthe loss of methyl methacrylate monomer by evaporation is considerably reduced.
Example 5 An 80/ 60 unfinished cotton fabric was immersed in a 15% solution of sodium hydroxide for 10 minutes. It was then squeezed out and washed thoroughly in anhydrous methyl alcohol. After drying it was treated with a 10%'solution of polymerized methyl methacrylate in acetone, squeezed 2 aoaaaes out and dried. It was then wet out and dried by ironing. An unusually white and somewhat lustrous finish was obtained which was not removed by boiling for one-half hour in 0.5% soap solution.
Example 6 A skein of gel rayon yarn (made up of filaments which have not been dried after coagulation and desulfurization) was washed in water-free acetone until substantially free of water, then treated with a 5% solution of polymerized methyl methacrylate in acetone. The excess solution was carefully removed by pressing the skein between sheets of absorbent material. The treated fibers were found to have a greater elastic recovery and were stiffer and more wear resistant than the untreated fibers.
When the above examples are repeated using mixtures of methyl methacrylate and its homologues, such as ethyl methacrylate or proply methacrylate, the finished materials possess satisfactory fastness to laundering and a pleasing white appearance.
When the aforementioned experiments are repeated utilizing other alkyl alkacrylates and mixtures thereof, but omitting therefrom methyl methacrylate, the results are superior to the results obtained whe starch or similar sizing agents are utilized but are less satisfactory than in the case of the preceding examples.
It is to be understood that the aforementioned examples are illustrative merely of the manner of carrying out the practical application of the present invention. They are not intended to be considered as a limitation uopn the scope of this invention since the individual agents and the methods of applicatoin may be varied widely without departing from the scope hereof. For example, the sizing agent selected in accordance with this invention may be applied to the fibers in unpolymerized, partially polymerized or completely polymerized condition. In place of an individual alkyl alkacrylate a mixture of two or more may be selected. Where ethyl methacrylate and/or its higher homologues are used it is particularly advantageous to incorporate therewith methyl methacrylate. Beneficial results may also be obtained by incorporation of esters of higher alpha-alkylacrylic acids.
The sizing agents previously described may be applied to the textile materials in a variety of ways, and the invention is not to be restricted to any given method of sizing such materials. In general, it is advisable to accomplish this sizing by passing the material to be treated through a dilute suspension or emulsion of the sizing agent. Solutions of these agents may be prepared by utilizing well known organic solvents and mixtures thereof, such as alcohols, esters, ketones, hydrocarbons, etc. Aqueous emulsions of the alkyl esters of alpha alkyl substituted acrylic acids may be prepared, for example, by the use of dispersing agents such as alkyl naphthalene sulfonic acids, their sodium salts, alkali metal salts of fatty acids, sodium petroleum sulfonate, sulfonated castor oil and other sulfonated vegetable oils, etc. The amount of sizing agent in this solution or emulsion may vary considerably depending upon the particular agent selected, the material to be treated and the degree ofstiifness desired. However, an amount ranging from about 0.5% to about 35% based upon the solution or emulsion, is ordinarily quite sufiicient.
Very satisfactory results have been obtained by applying the sizing agent to the textile materials in an unpolymerized condition and causing polymerization to take place thereon. This may conveniently be accomplished by incorporating in a sizing solution or emulsion a small quantity of a polymerizing. agent. Such agents are 5 advisably those which are capable of giving oil oxygen such as organic peroxides, ozonides, and in particular benzoyl peroxide.
Furthermore, the sizing solution or suspension may contain additional materials such as plas- 10 ticizers. A representative few of the many plasticizers which are suitable for use herein are camphor, phthalates such as ethyl-, propyl, isopropyl-, butyl-, isobutyl-, cyclohexyl-, dibutyl-, esters of dibasic acids, etc. For the sake of 15 brevity additional plasticizers and combinations thereof as well as additional modifications of other features of the present invention will not be given in detail herein, since one familiar with the art should have no difiiculty in carrying out 20 this invention in accordance with the instructions hereof. For a very detailed description of the numerous modifications of this invention reference may be had to copendlng application Serial No. 759,744, filed Dec. 29, 1934. 25
The use of protective colloids in producing dispersions of methyl methacrylate monomers and related alkyl alkacrylate derivatives is particularly helpful. As mentioned in Example 2, gum tragacanth is well adapted for this purpose. 30 However, the invention is not restricted thereto since other well known protective colloids may be substituted therefor or used in admixture therewith. A representative few of these compounds are, for example, casein, gelatin, glue, Russian isinglass, Irish moss, etc.
Dispersions of, for example, polymeric methyl methacrylate, may readily be obtained by dissolving said compound in an organic solvent, adding thereto a suitable dispersing agent, and 40 then adding water under continuous violent agitation. Likewise, dispersions may be obtained in an internal mixer, such as a Bunbury mill, by working the compound to be dispersed with a dispersing agent and a protective colloid, and dilut- 45 ing with water to the desired solids content.
Textile materials to be sized may be derived from animal, synthetic or vegetable sources. The term textile materials" when used herein is understood to include woven, knitted and ma 50 terial otherwise fabricated from fibers, threads, filaments, etc., of silk, artificial silk, cotton, wool, linen, jute, etc. After passing the aforementioned or related materials through the sizing bath they may be run through squeeze rolls to 55 remove excess solution and to improve the penetratlon of the solution into the material. The solvent or dispersing medium may then be evaporated therefrom, or if a water-soluble solvent is used, the resin may be precipitated on the 60 textile material by immersing said material in water. Finally, the treated article may be ironed or calendered.
By means of the present invention the disadvantages of prior art sizing agents are overcome 35 to a great extent. The process is both speedy and eflicient, and results in a surprisingly white product of pleasing feel and appearance. The product possesses exceptional fastness to laundering, and retains its superior characteristics after 7 repeated launderings.
As many apparently widely different embodiments of this invention may be made without departing from the spirit and scope thereof, it is to be understood that the invention is not limited 75 to the specific embodiments thereof except as delined in the appended claims.
I claim:
1. Textile materials sized with alkyl alkacrylate polymers.
2. Cellulosic textile materials sized with alkyl methacrylate polymers.
3. Textile materials sized with methyl methacrylate polymers.
4. Cellulosic textile materials sized with methyl methacrylate polymers.
5. Cotton fabrics sized with methyl methacrylate polymers.
6. A process for sizing textile materials which comprises passing said materials through a liquid containing an alkyl alkacrylate and subsequently evaporating the liquid from the treated material.
'I. A process for sizing textile materials which comprises passing said materials through a liquid containing methyl methacrylate polymers and subsequently evaporating the liquid from the treated material.
8. A process for sizing textile materials which comprises passing said materials through a liquid containing methyl methacrylate monomer and a polymerizing agent and subsequently evaporating the liquid from the treated material and polymerizing the methyl methacrylate monomer.
9. A process for sizing textile materials which comprises passing said materials through a liquid containing methyl methacrylate monomer and benzoyl peroxide and subsequently evaporating the liquid from the treated material and polymerizing the methyl methacrylate monomer.
DANIEL E. STRAIN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US759743A US2046885A (en) | 1934-12-29 | 1934-12-29 | Textile material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US759743A US2046885A (en) | 1934-12-29 | 1934-12-29 | Textile material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2046885A true US2046885A (en) | 1936-07-07 |
Family
ID=25056790
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US759743A Expired - Lifetime US2046885A (en) | 1934-12-29 | 1934-12-29 | Textile material |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2046885A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE747465C (en) * | 1937-01-17 | 1944-09-27 | Jung & Simons | Process for waterproofing and crease-proofing textile webs made of cellulose or cellulose hydrate fibers |
| US2525476A (en) * | 1946-12-14 | 1950-10-10 | Dan River Mills Inc | Process for laminating starch-free resin sized fabrics |
| US2540048A (en) * | 1943-11-16 | 1951-01-30 | Interchem Corp | Dyed textiles and methods and composition for producing same |
| US2606810A (en) * | 1949-09-28 | 1952-08-12 | American Cyanamid Co | Treatment of wool-containing textile materials and products thereof |
| US2674741A (en) * | 1951-03-21 | 1954-04-13 | Cluett Peabody & Co Inc | Shirt collar |
| US2807865A (en) * | 1954-06-14 | 1957-10-01 | Rohm & Haas | Sized textile and method of fabricating yarn into fabric |
| US2895950A (en) * | 1955-08-25 | 1959-07-21 | American Sealants Company | Compositions containing hydroperoxide polymerization catalyst and acrylate acid diester |
| US3085907A (en) * | 1958-04-01 | 1963-04-16 | Rohm & Haas | Aqueous polymeric methyl methacrylate compositions for coating cement products and methods for coating such products |
-
1934
- 1934-12-29 US US759743A patent/US2046885A/en not_active Expired - Lifetime
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE747465C (en) * | 1937-01-17 | 1944-09-27 | Jung & Simons | Process for waterproofing and crease-proofing textile webs made of cellulose or cellulose hydrate fibers |
| US2540048A (en) * | 1943-11-16 | 1951-01-30 | Interchem Corp | Dyed textiles and methods and composition for producing same |
| US2525476A (en) * | 1946-12-14 | 1950-10-10 | Dan River Mills Inc | Process for laminating starch-free resin sized fabrics |
| US2606810A (en) * | 1949-09-28 | 1952-08-12 | American Cyanamid Co | Treatment of wool-containing textile materials and products thereof |
| US2674741A (en) * | 1951-03-21 | 1954-04-13 | Cluett Peabody & Co Inc | Shirt collar |
| US2807865A (en) * | 1954-06-14 | 1957-10-01 | Rohm & Haas | Sized textile and method of fabricating yarn into fabric |
| US2895950A (en) * | 1955-08-25 | 1959-07-21 | American Sealants Company | Compositions containing hydroperoxide polymerization catalyst and acrylate acid diester |
| US3085907A (en) * | 1958-04-01 | 1963-04-16 | Rohm & Haas | Aqueous polymeric methyl methacrylate compositions for coating cement products and methods for coating such products |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3462296A (en) | Fluorinated oil- and water-repellent copolymer and process for treating fibrous materials with said copolymer | |
| US2344671A (en) | Higher molecular alcohols | |
| US3361695A (en) | Film-forming copolymers from acrylates, acrylic acid and n-methylolmethacrylamide | |
| US2343091A (en) | Treatment of textiles and composition useful therefor | |
| US2835641A (en) | Aqueous emulsions for the preparation of water repellent dressings and process of treating fibrous materials therewith | |
| US2343090A (en) | Treatment of textiles and composition useful therefor | |
| US2046885A (en) | Textile material | |
| US2469407A (en) | Treatment of textile materials | |
| US2343089A (en) | Treatment of textiles and composition useful therefor | |
| US2284895A (en) | Treatment of textiles to impart water-repellence | |
| US2047218A (en) | Compositions comprising deacetylated chitin | |
| US3096524A (en) | Process for improving crease-retention properties of cotton garments | |
| US4116625A (en) | Process for modifying fibrous products containing cellulosic fibers | |
| US3446761A (en) | Stain-resistant article,and composition for preparing same | |
| US2328431A (en) | Process for rendering textile materials water repellent | |
| US2343094A (en) | Treatment of textiles and composition useful therefor | |
| US2499653A (en) | Treatment of protein-containing textile materials and products thereof | |
| US2411818A (en) | Process for treating cellulose-containing textiles | |
| US2530175A (en) | Stabilization of regenerated cellulose | |
| US2318429A (en) | Aqueous dispersion of polymerized alkyl methacrylate and method of preparing same | |
| US3428617A (en) | Cationic hydroxy-containing polymers,preparation and use | |
| US2368948A (en) | Process for increasing the transparency of fabrics containing filament yarns | |
| US3245831A (en) | Process of finishing textiles with mechanically stable latex of emulsified particles of emulsion-polymerized nonoxidized polyethylene | |
| DE2536810A1 (en) | METHOD FOR TREATMENT OF FABRICS | |
| US4152507A (en) | Process for modifying fibrous products containing cellulosic fibers |