US3427121A - Wrinkle-resistant cotton fabrics with improved moisture absorption - Google Patents

Wrinkle-resistant cotton fabrics with improved moisture absorption Download PDF

Info

Publication number
US3427121A
US3427121A US290264A US3427121DA US3427121A US 3427121 A US3427121 A US 3427121A US 290264 A US290264 A US 290264A US 3427121D A US3427121D A US 3427121DA US 3427121 A US3427121 A US 3427121A
Authority
US
United States
Prior art keywords
fabric
cotton
wrinkle
moisture absorption
additive
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
Application number
US290264A
Inventor
John G Frick Jr
Andrew G Pierce Jr
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
US Department of Agriculture USDA
Original Assignee
US Department of Agriculture USDA
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by US Department of Agriculture USDA filed Critical US Department of Agriculture USDA
Application granted granted Critical
Publication of US3427121A publication Critical patent/US3427121A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423Amino-aldehyde resins

Definitions

  • the object of this invention is to provide a simple method of producing cotton fabrics with a high degree of wrinkle-resistance, and wash-Wear properties, and with little or no reduction in moisture absorptivity. It has been found that this can be accomplished by using ordinary methylol amide finishing agents in the usual procedure but with a nonvolatile, water-soluble organic compound included in the treatment.
  • the amount of this additive compound is adjusted to be sufiicient to maintain enough swelling of the cotton fiber to give improved moisture absorption but not to be great enough to prevent the development of wrinkle resistance in the treated fabric when in the dry state.
  • the compound used as the additive also must have low reactivity toward the methylol amide finishing agent, or else the stabilizing action of the agent will be inhibited or entirely eliminated.
  • Suitable compounds for use as additives in this invention are the polyethylene glycols and their monoalkyl or dialkyl ethers, such as: tetraethylene glycol dimethyl ether, triethylene glycol monoethyl ether, and polyethylene glycols with molecular weight greater than 200.
  • the amount of the additive compound suitable for use will range from 3 to 15% of the treating solution, with 5.0 to 7.5% the preferred quantity.
  • a solution will be prepared containing 5 to 10% methylol amide, 0.3 to 3.0% catalyst to promote reaction of the methylol amide, 7 to 10% additive compound described in the invention, and the remainder water. Minor proportions of other agents may also be included, such as those to modify the feel or hand of the treated fabric.
  • the cotton fabric is impregnated with the solution described by soaking and squeezing between pad rolls .until the amount of solution retained is 50 to of the dry fabric weight.
  • the fabric is dried and heated briefly at an elevated temperature, 1 to 3 minutes at to C., to cause reaction of the methylol amide agent. In most instances it is preferable to wash the fabric after this treatment.
  • the cotton fabric has had a degree of wrinkle-resistance imparted to it that is only slightly less than that obtained without the use of the additive described in this invention.
  • the moisture absorption of the fabric is substantially higher than that of a fabric treated without the use of the additive.
  • the moisture absorption of fabric treated by the process of this invention often approaches and sometimes exceeds that of the untreated fabric.
  • Example 1 Five solutions were prepared and used for the treatment of cotton print cloth. Each solution contained 10% dimethylol ethyleneurea, 0.5% zinc nitrate hexahydrate and an amount of tetraethylene glycol dimethyl ether ranging from 0 to 15 as additive. The solutions were applied to samples of the fabric, and the samples dried at 60 C. for 7 minutes, heated at 160 C. for 3 minutes, washed and dried. The fabrics were tested for moisture regain and crease recovery angle using methods described by the American Society for Testing Materials, "ASTM Standards on Textile Materials. Crease recovery angle is used as a measure of wrinkle resistance. The same crease recovery test was given to the fabrics while they were wet with water as a measure of their smooth drying properties. Results of the testing are shown in the following table.
  • Example 2 A series of solutions was prepared as in Example 1 except that triethylene glycol monoethyl ether was used as the additive. The solutions were applied to cotton fabric to obtain the results shown in the following table.
  • Example 3 A solution was prepared containing 10% dimethylol ethylene-urea, 0.5% zinc nitrate hexahydrate, and 10% of a polyethylene glycol with an average molecular weight of 350. Application of this solution to cotton fabric followed by drying, heating, and an afterwash, produced a fabric with 275 crease recovery angle and 5.5% moisture regain. A similar solution, but without the polyethylene glycol, produced a fabric with 280 crease recovery angle and 5.3% moisture regain.
  • Example 4 A series of solutions was prepared containing 10% of different finishing agents and an appropriate amount of catalyst for the agent. A second series of solutions was prepared similarly but with 7.5% of tetraethylene glycol dimethyl ether as additive in each. Both series were applied to samples of cotton fabric, dried, heat cured, and washed. Test results on these fabric samples are shown in the following table.
  • Moisture regain Crease recovery (percent) angles 1 Agent used Without With Without With additive additive additive additive Dimethylol ethyleneurea 5. 7 6. 9 279 256 Dimethylol ethyl carbamate- 5. 5 6. 5 255 232 Dimethylol triazone 6. 4 7. 0 234 236 Polymethylol melamine 5. 5 7. 0 262 254 Untreated fabric 6. 7 184 1 Warp angle plus filling angle.

Description

United States Patent 3,427,121 WRINKLE-RESISTANT COTTON FABRICS WITH IMPROVED MOISTURE ABSORPTION John G. Frick, Jr., and Andrew G. Pierce, Jr., New Orleans, La., assignors to the United States of America as represented by the Secretary of Agriculture No Drawing. Filed June 24, 1963, Ser. No. 290,264 US. Cl. 8-115.6 1 Claim Int. Cl. D06c 29/00; D06m 1/00 A nonexclusive, irrevocable, royalty-free license in the invention herein described, throughout the world for all purposes of the United States Government, with the power to grant sublicenses for such purposes, is hereby granted to the Government of the United States of America.
The treatment of cotton fabrics to give them wrinkle resistance and wash-Wear or smooth drying properties is a common operation. These treatments usually consist of the application to the fabric of chemical agents that can react with themselves or the cellulose of cotton and fix the structure of the cotton fiber. The fabric is stabilized thereby in a smooth form, to which it will return after a deformation such as creasing or wrinkling. For these treatments, the most common agents now in use are the methylol amide compounds formed by the reaction of formaldehyde with polyfunctional organic amides. Some examples are dimethylol ethyleneurea, dimethylol ethyltriazone, trimethylol melamine, and the methylol ureas.
There are some disadvantages in these treatments, however. One disadvantage is that the moisture absorptivity of the cotton is reduced by the treatment. The relatively high moisture absorption normally present in cotton is often desirable. In cotton garments, it allows greater takeup and dissipation of body moisture, and contributes thereby to the comfort of the wearer, particularly in humid weather. This has been a marked advantage that cotton fabrics possessed in comparison with fabrics made from fibers with an inherently poor moisture absorption. The usual wrinkle resistance treatments, by reducing moisture absorptivity, gives a fabric that will make a less comfortable garment than untreated cotton fabric would make.
It is known that the loss of moisture absorptivity in these treatments can be prevented by conducting the treatment in a manner that allows the cotton to stay swollen throughout, for instance by conducting the treatment while the cotton remains wet with water. Treatments conducted in this manner, however, usually do not give the fabric much ability to resist wrinkling in the dry state, the condition in which it is normally used. In the few instances such treatments have given wrinkle resistance, the required procedure has proven troublesome and expensive.
The object of this invention is to provide a simple method of producing cotton fabrics with a high degree of wrinkle-resistance, and wash-Wear properties, and with little or no reduction in moisture absorptivity. It has been found that this can be accomplished by using ordinary methylol amide finishing agents in the usual procedure but with a nonvolatile, water-soluble organic compound included in the treatment. The amount of this additive compound is adjusted to be sufiicient to maintain enough swelling of the cotton fiber to give improved moisture absorption but not to be great enough to prevent the development of wrinkle resistance in the treated fabric when in the dry state. The compound used as the additive also must have low reactivity toward the methylol amide finishing agent, or else the stabilizing action of the agent will be inhibited or entirely eliminated. Suitable compounds for use as additives in this invention are the polyethylene glycols and their monoalkyl or dialkyl ethers, such as: tetraethylene glycol dimethyl ether, triethylene glycol monoethyl ether, and polyethylene glycols with molecular weight greater than 200. The amount of the additive compound suitable for use will range from 3 to 15% of the treating solution, with 5.0 to 7.5% the preferred quantity.
Application of treatments with these additives to cotton fabric is by the same means commonly employed at present in wrinkle resistance treatments. In a typical treatment, a solution will be prepared containing 5 to 10% methylol amide, 0.3 to 3.0% catalyst to promote reaction of the methylol amide, 7 to 10% additive compound described in the invention, and the remainder water. Minor proportions of other agents may also be included, such as those to modify the feel or hand of the treated fabric. The cotton fabric is impregnated with the solution described by soaking and squeezing between pad rolls .until the amount of solution retained is 50 to of the dry fabric weight. The fabric is dried and heated briefly at an elevated temperature, 1 to 3 minutes at to C., to cause reaction of the methylol amide agent. In most instances it is preferable to wash the fabric after this treatment.
After such a treatment it is found that the cotton fabric has had a degree of wrinkle-resistance imparted to it that is only slightly less than that obtained without the use of the additive described in this invention. The moisture absorption of the fabric, however, is substantially higher than that of a fabric treated without the use of the additive. In fact, the moisture absorption of fabric treated by the process of this invention often approaches and sometimes exceeds that of the untreated fabric.
In the following examples the process and results of this invention are described in greater detail.
Example 1 Five solutions were prepared and used for the treatment of cotton print cloth. Each solution contained 10% dimethylol ethyleneurea, 0.5% zinc nitrate hexahydrate and an amount of tetraethylene glycol dimethyl ether ranging from 0 to 15 as additive. The solutions were applied to samples of the fabric, and the samples dried at 60 C. for 7 minutes, heated at 160 C. for 3 minutes, washed and dried. The fabrics were tested for moisture regain and crease recovery angle using methods described by the American Society for Testing Materials, "ASTM Standards on Textile Materials. Crease recovery angle is used as a measure of wrinkle resistance. The same crease recovery test was given to the fabrics while they were wet with water as a measure of their smooth drying properties. Results of the testing are shown in the following table.
The tabulated data show that the use of 3 or 5% addi-- tive has no effect on the crease recovery produced by the treatment in dry fabric, but that moisture regain is increased. Even with 10% or 15% additive the crease recovery is considerably higher than that of untreated fabric, and the moisture regain is increased. Wet crease recovery increases with additive concentration up to 15%, the highest used. Example 2 A series of solutions was prepared as in Example 1 except that triethylene glycol monoethyl ether was used as the additive. The solutions were applied to cotton fabric to obtain the results shown in the following table.
I Additive in soln. Moisture regain Crease recovery (percent) (percent) (deg. W dz F), dry
. The results show that triethylene glycol monoethyl ether is also an effective additive.
Example 3 A solution was prepared containing 10% dimethylol ethylene-urea, 0.5% zinc nitrate hexahydrate, and 10% of a polyethylene glycol with an average molecular weight of 350. Application of this solution to cotton fabric followed by drying, heating, and an afterwash, produced a fabric with 275 crease recovery angle and 5.5% moisture regain. A similar solution, but without the polyethylene glycol, produced a fabric with 280 crease recovery angle and 5.3% moisture regain.
Example 4 A series of solutions was prepared containing 10% of different finishing agents and an appropriate amount of catalyst for the agent. A second series of solutions was prepared similarly but with 7.5% of tetraethylene glycol dimethyl ether as additive in each. Both series were applied to samples of cotton fabric, dried, heat cured, and washed. Test results on these fabric samples are shown in the following table.
Moisture regain Crease recovery (percent) angles 1 Agent used Without With Without With additive additive additive additive Dimethylol ethyleneurea 5. 7 6. 9 279 256 Dimethylol ethyl carbamate- 5. 5 6. 5 255 232 Dimethylol triazone 6. 4 7. 0 234 236 Polymethylol melamine 5. 5 7. 0 262 254 Untreated fabric 6. 7 184 1 Warp angle plus filling angle.
References Cited UNITED STATES PATENTS Re. 24,011 5/ 1955 Ericks 8115.6 3,046,079 7/1962. Reeves et a1 8--1l6.4 3,181,927 5/ 196-5 Roth et a1 8116.3 OTHER REFERENCES Valko et al.: Textile Research Journal, vol. 32, pp. 331- 337 (1962).
Angelil, M. F.: Addition of Polyglycols to Cross-Linking Reagents for Cotton, Masters Thesis submitted to Lowell Technological Institute, May 24, 1960. (See pp. 9-11.)
NORMAN G. TORCHIN, Primary Examiner.
J. CANNON, Assistant Examiner.
US. Cl. X.R.

Claims (1)

1. IN A PROCESS FOR TREATING COTTON FABRTICS WITH NITROGENCONTAINING RESINS, THE IMPROVEMENT WHICH CONSISTS OF INCORPORATING INTO THE RESIN-TREATING FORMULATION A QUANTITY OF FROM ABOUT 5.0% TO ABOUT 7.5% OF TETRAETHYLENE GLYCOL DIMETHYL ETHER.
US290264A 1963-06-24 1963-06-24 Wrinkle-resistant cotton fabrics with improved moisture absorption Expired - Lifetime US3427121A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US29026463A 1963-06-24 1963-06-24

Publications (1)

Publication Number Publication Date
US3427121A true US3427121A (en) 1969-02-11

Family

ID=23115218

Family Applications (1)

Application Number Title Priority Date Filing Date
US290264A Expired - Lifetime US3427121A (en) 1963-06-24 1963-06-24 Wrinkle-resistant cotton fabrics with improved moisture absorption

Country Status (1)

Country Link
US (1) US3427121A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3656885A (en) * 1967-11-15 1972-04-18 Cotton Inc High strength wrinkle resistant cotton fabrics produced by a process involving both monosubstitution and crosslinking of the cotton
US3707692A (en) * 1969-03-10 1972-12-26 Mc Graw Edison Co Method of treating cellulosic material to improve the usefulness thereof as an insulator in electrical apparatus
US3936561A (en) * 1974-04-02 1976-02-03 West Point-Pepperell, Inc. Anti-dusting treatment of textiles
US6544296B2 (en) 2000-02-07 2003-04-08 The Proctor & Gamble Company Enhanced fabric comprising substrates and process to provide same
US6953485B2 (en) 2000-02-07 2005-10-11 Strike Investments, Llc Enhanced fabric comprising substrates and process to provide same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE24011E (en) * 1949-07-07 1955-05-31 Product thereof
US3046079A (en) * 1960-05-24 1962-07-24 Wilson A Reeves Process of reacting partially swollen cotton textiles with aqueous solutions of specific aldehydes containing acid catalysts to produce wet and dry crease resistance
US3181927A (en) * 1959-11-16 1965-05-04 American Cyanamid Co Process of wet and dry wrinkleproofing cellulose fabric with an aminoplast resin and zinc chloride

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE24011E (en) * 1949-07-07 1955-05-31 Product thereof
US3181927A (en) * 1959-11-16 1965-05-04 American Cyanamid Co Process of wet and dry wrinkleproofing cellulose fabric with an aminoplast resin and zinc chloride
US3046079A (en) * 1960-05-24 1962-07-24 Wilson A Reeves Process of reacting partially swollen cotton textiles with aqueous solutions of specific aldehydes containing acid catalysts to produce wet and dry crease resistance

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3656885A (en) * 1967-11-15 1972-04-18 Cotton Inc High strength wrinkle resistant cotton fabrics produced by a process involving both monosubstitution and crosslinking of the cotton
US3707692A (en) * 1969-03-10 1972-12-26 Mc Graw Edison Co Method of treating cellulosic material to improve the usefulness thereof as an insulator in electrical apparatus
US3936561A (en) * 1974-04-02 1976-02-03 West Point-Pepperell, Inc. Anti-dusting treatment of textiles
US6544296B2 (en) 2000-02-07 2003-04-08 The Proctor & Gamble Company Enhanced fabric comprising substrates and process to provide same
US6953485B2 (en) 2000-02-07 2005-10-11 Strike Investments, Llc Enhanced fabric comprising substrates and process to provide same

Similar Documents

Publication Publication Date Title
US3357784A (en) Exposure to intense ultraviolet light to improve characteristics of cellulosic fabrics in divinyl sulfone and glyoxal cross-linking processes
US2901463A (en) Compositions, textiles treated therewith and processes for the treatment thereof
US3144299A (en) Wrinkle resistance finish for cellulosic textiles
US3427121A (en) Wrinkle-resistant cotton fabrics with improved moisture absorption
US3441367A (en) Method for setting finishes on cellulosic textiles with catalyst composition of magnesium halide and organic acid
US3546006A (en) Wet-fixation process for cellulosic fabrics using low add-ons of resins
US3015584A (en) Wrinkle resistance treatment for cellulosic textile fabrics
US3181927A (en) Process of wet and dry wrinkleproofing cellulose fabric with an aminoplast resin and zinc chloride
US3933426A (en) Process for making textiles containing cellulose crease-resistant
US3617195A (en) Textile finishing process using a chlorinated hydrocarbon as the reactant solvent
US3642428A (en) Vapor phase resin fixation process for cellulosic material permitting subsequent cure
US3441366A (en) Wrinkle-resistant cotton fabrics with improved moisture absorption
US3026216A (en) Treatment of textile fabrics with methylglycidyl ethers
US3606992A (en) Abrasion and wrinkle resistant cotton containing fabric and method of manufacture
US2378724A (en) Textile finishing and composition therefor
US3634019A (en) Metal acetate-acidic catalyst system for cellulosic fabric treatment
US3451763A (en) Cellulose-containing fabrics and process therefor
US2839506A (en) Antistatic treatment for hydrophobic synthetic fiber-containing materials
US3153003A (en) Aqueous dispersion of an aminoplast and an epoxy compound
US3877872A (en) Process for improving abrasion resistance of resilient fabrics and the product produced
US3533728A (en) Inorganic and/or organic cellulose swelling agents used in conjunction with cross-linking agents in fabric modification process
US3518044A (en) Process for producing wrinkle resistant carbamate-modified cellulosic textile materials by catalysis with hydrogen halide gas
US3254940A (en) Cellulosic textile finishing process and product
GB871105A (en) Improvements in the incorporation of thermosetting synthetic resins in linen textilefabrics
US3002859A (en) Compositions, textiles treated therewith and processes for the treatment thereof