US2329651A - Stabilization of knit fabrics - Google Patents
Stabilization of knit fabrics Download PDFInfo
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- US2329651A US2329651A US339591A US33959140A US2329651A US 2329651 A US2329651 A US 2329651A US 339591 A US339591 A US 339591A US 33959140 A US33959140 A US 33959140A US 2329651 A US2329651 A US 2329651A
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
Definitions
- This invention relates to the stabilization of knitted cellulose fabrics against excessive or marked change in dimensions and against distortion without embrittlement of the yarns and with retention of the soft hand, freeness, and elasticity which are required for knit goods.
- Another method that has been proposed for reducing shrinkage of woven fabric is based on impregnating with a considerable amount of a heat-hardenable resin or resin-forming material, such as methylol urea, and forming the hardened resin within the fibers.
- a heat-hardenable resin or resin-forming material such as methylol urea
- the cloth after impregnation with the resinous material, is dried under tension at the desired marketable dimensions and the resin is cured while these dimensions are maintained.
- Such methods are not applicable to knit fabrics, not only because of the differences in construction already mentioned but also because of undesirable efi'ects imparted by such procedure and by the resins heretofore used.
- the condensates which have been found effective for this process are formed by reacting urea, formaldehyde, and one of the monoor poly-hydric alcohols which in the presence of an acid catalyst react therewithto form water-soluble condensates.
- the alcohols which yield water-soluble condensates include methyl alcohol, ethyl alcohol, propyl or isopropyl alcohol, ethylene glycol, diethylene glycol, glycerine, dextrose, etc., the polyhydric alcohols yielding particularly effective condensates.
- a simple condensate of urea and formaldehyde may first be prepared and then reacted with the hydroxyl-bearing compound. Alternatively the reactants may be directly combined. The reaction.
- the solution of condensatej may be applied to the knitted fabric by.dipping,. spraying, orother means suitable for saturating it with'the solution.
- the wet fabric is then opened out and snread flat preferablmln the case of the usual
- the tubular knit fabric by running it over an internal device or shoe which is set to spread the fabric to approximately the finished width which is desired or a slightly wider width. It is then passed between squeeze rolls which express excess solution and which are adjusted to leave only 50% to 80% solution in the fabric. These percentages are based on dry weight of the fabric.
- the concentration of the impregnating solution is preferable to adjust the concentration of the impregnating solution to between about 8% and 12% of condensate solids and to leave in the cotton only enough condensate to yield from about to about 8% resin after the subsequent treatments, although slightly higher resin contents are sometimes permissible.
- there may be used solutions with as much as 15% condensate solids and the amount of solution retained may desirably be increased somewhat over that in a cotton fabric, an amount of resin in the final fabric between 6% and 12% being particularly satisfactory.
- Example 1 A 16" tubular knit, 5 /2 yd./lb., 305 yarn, cotcontaining 12% urea-formaldehyde glycol condensate, 0.3% of ammonium chloride, and 0.1%
- Example 2 A 17 tubular knit, 5 yd./lb. all-spun viscose rayon fabric, peroxide-bleached, scoured, dyed, and dried, was dipped into a solution containing 15% of a urea-formaldehyde-glycol condensate, 0.3% of ammonium thiocyanate and 0.05% sodium octylphenoxyethyl sulfate. The wet fabric was'spread to a width of 18 /2 inches with a flat shoe operating within the tubular fabric, squeezed throug ⁇ pair of rolls to leave an 80% ain in weight ased on the dry fabric, and batch-rolled. -'The' fabric was then fed into a carrier drier operating at 250 F. to 260 F. and then into a similar drier operating at 300 F. to heat-harden the condensate.
- the resulting fabric exhibited comparatively a small degree of shrinkage, whether tested by home washing methods or in commercial laundry units.
- the fabric possessed a full hand an resilience without ragginess, and yet was soft and pleasing to the hand.
- Example 3 A 17 /2" tubular knit, spun cuprammonium rayon and cotton mixed fabric, 5 yds./lb., peroxide-bleached, soap-washed, and dried, was
- This fabric was made into garments which were, subjected to wash tests in order to deter-' mine the shrinkage of the resin-containing knit fabric compared to the shrinkage of the usual untreated knit fabric.
- Untreated garments 9 Treated garments when other sets of garments werewashedin s Garments washed in a domestic type washing machine with a 0.2% oap v sprayed with a solution. containing 10% of a urea-formaldehyde-glycol condensate, 0.2% of ammonium sulfate, and 0.07% of sodium octylphenoxyethoxyethoxyethyl sulfonate. The fabric was passed through-two sets of rubber brass squeeze rolls, with the final set adjusted to leave an pick-up of solution.
- the fabric was spread with an internal shoe to a widthof 18%" and passed througha carrierldrier at a temperature of about 260 F.
- the dry fabric was passed into a loop drier operating at 310 F. where the condensate was cured.
- Example 4 A 27" tubular knit, 3 yds./lb., cotton fabric, peroxide-bleached, dyed with direct dyestuff, soap-washed and dried to width, was spread to a width of 28 inches over a flat internal shoe immediately before being wet outon a slop padder with a solution containing 10% of a water-soluble urea-formaldehyde-ethyl alcohol condensate, 0.2% of ammonium chloride, and 0.1% of the sodium salt of octylphenoxyethyl sulfate. The temperature of the solution was maintained between and F. The wet fabric was then passed through a-set of squeeze rolls, which removed excess solution leaving 80% solution in the goods, based on the dry weight of the fabric.
- the cloth was thendried at 260 F. by running aaaacor curing box, which operated at a temperature of 310 F.
- the cured fabric was then dipped in a solution containing 0.1% of the sodium salt of octylphenoxyethyl sulfate and 0.1% of sodium perborate, spread, squeezed and dried in a carrier-type drier.
- the resin-containing fabric when out into garments exhibited considerably less shrinkage than untreated fabric in garments, whether tested by a commercial laundry procedure or by a home washing procedure.
- the treated fabric possessed the soft, full hand required for knit goods. There was, furthermore, a marked increase in the washfastness of the direct dyestuif in the treated fabrics.
- Heavier fabrics than shown in the above examples may be successfully stabilized by the same general procedure, but with an increase in the time allowed for the steps of penetrating, drying, and curing.
- the stabilized fabrics may be treated with softeners, such as sulfonated olive oil, tea-seed oil, castor oil, tallow, etc., or a sulfated long chain aliphatic alcohol, etc., with water-proofing agents, sizing agents or both permanent and non-permanent types, etc.
- the stabilized fabrics furthermore, may be subjected to mechanical treatments, such as'preshrinking, with a far greater degree of success than has heretofore been possible.
- the process herein described may be successfully applied to knit cellulose fabrics, composed of cotton, or regenerated cellulose, including both viscose and cuprammonia fibers as filaments or staple fibers, or mixtures of these various materials.
- a process for stabilizing knitted cellulose fabric against marked change in dimensions and against distortion of the construction with retention of elasticity, resilience, and freeness of construction which comprises impregnating said fabric with an aqueous solution containing 8 to 15% of a water-soluble condensate of urea, formaldehyde, and an alcohol and a small amount of a strong acid-type catalyst, removing excess solution from the fabric to leave to 12% of said condensate in the fabric, based on dry weights, spreading the fabric to approximatel the desired finished width, drying the spread fabric without tension, and heat-hardening the condensate in the fabric.
- a process for stabilizing knitted cellulose fabric againstmarked change in dimensions and against distortion of the construction with retention of elasticity, resilience, and freeness of construction which comprises impregnating said fabric with an aqueous solution containing 8 to 15% of a water-soluble condensate of urea, formaldehyde, and ethylene glycol together with a small amount of a strong acid-type catalyst, spreading the impregnated fabric to approximately the-desired finished with, squeezing it to leave therein a condensate content of 5% to 12% based on the weight of the dry fabric, drying the spread fabric without tension, and heat-hardening the condensate in the fabric.
- a process for stabilizing knitted cellulose fabric against marked change in dimensions and against distortion of the construction with retention of elasticity, resilience, and freeness of construction which comprises impragnating said fabric with an aqueous solution containing 8 to 15% of a water-soluble condensate of urea, formaldehyde and ethylene glycol together with a small amount of an ammonium salt of a strong acid, spreading the impregnated fabric to approximately the desired finished width, squeezing it to leave therein a condensate content of 5% to 12% based on the weight of the dry fabric, drying the spread fabric without tension, and heat-hardening the condensate in the fabric.
- a process for stabilizing knitted cotton fabric against marked change in dimensions and against distortion of the construction with retention of elasticity, resilience, and freeness of construction which comprises impregnating said fabric with an aqueous solution containing 8 to 12% of a water-soluble condensate of urea, formaldehyde, and ethylene glycol together with a small amount of a strong acid-type catalyst, spreading the impregnated fabric to approximately the desired finished width, squeezing it to leave therein a condensate content of 5 to 8% based on the weight of the dry fabric, drying the spread fabric without tension, and heat-hardening the condensate in the fabric.
- a process for stabilizing knitted cotton fabric against marked change in dimensions and against distortion of the construction with retention of elasticity, resilience, and freeness ofconstruction which comprises impregnating said fabric with an aqueous solution containing 8 to 12% of a water-soluble condensate of urea, formaldehyde, and a polyhydric alcohol together with a 1 based on the weight of the dry fabric, drying the spread fabric without tension, and heat-harden!- ing the condensate inthe fabric.
- freeness of construction which comprises impregnating said fabric with an aqueous solution containing 8 to 15% of a water-soluble condensate of urea, formaldehyde, and ethylene glycol together with a small amount of a strong acid-type catalyst, spreading the impregnated fabric to approximately the desired finished width, squeezing it to leave therein a condensate content of 6 to 12% based on the weight of the dry fabric, drying the spread fabric without tension, and heat-hardening the condensate in the fabric.
- a process for stabilizing knitted regenerated cellulose fabric against marked change in dimensions and against distortion of theconstruction with retention of elasticity, resilience, and freeness of construction which comprises impregnating said fabric with an aqueous solution containing 8 to 15% of a water-soluble condensate of urea, formaldehyde, and a polyhydric alcohol together with a small amount of a strong acid-type catalyst, spreading the impregnated fabric to approximately the desired finished width, squeezing it to leave therein a condensate content of 6 to 12% based on the weight of the dry fabric, drying the spread fabric without tension, and heat-
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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
Patented Sept. 14, 1943 STABILIZATION OF KNITFABRICS Donald sell H. Powers, Moorestown, N. 1., and Bus- G. Lawrence, Philadelphia, Pa., assignors to Riihm & Haas Company, Philadelphia, Pa.
No Drawing. Application June 8, 1940, Serial No. 339,591
7 Claims.
This invention relates to the stabilization of knitted cellulose fabrics against excessive or marked change in dimensions and against distortion without embrittlement of the yarns and with retention of the soft hand, freeness, and elasticity which are required for knit goods.
No practical method for controlling the shrinkage of knit fabrics has heretofore been developed, primarily because of difliculties resulting from the peculiar construction of knit goods as compared to woven fabrics. These diiliculties are founded on a lack of rigid construction and a lack of selvage by which woven fabrics are readily handled. Knit goods depend for their value upon loose, free chains which permit stretching and impart elasticity. For this reason the knitted stitches must be free to slide over each other. The construction and the properties required of knitted fabrics render them especially susceptible to large changes in dimensions in both length and width and to distortion of the shape of the stitches.
While it is possible to impart an apparent shrinkage to knit fabric by purely mechanical treatment, the resulting fabric is seldom completely shrunk even though an exorbitant loss of yardage may have occurred. Furthermore, mechanical shrinking leaves knit fabrics susceptible and sensitive to stretching and distortion. However successful mechanical shrinkage of woven fabrics may have been, such a method has not been directly applicable to knit fabrics.
Another method that has been proposed for reducing shrinkage of woven fabric is based on impregnating with a considerable amount of a heat-hardenable resin or resin-forming material, such as methylol urea, and forming the hardened resin within the fibers. In order to control the shrinkage, the cloth, after impregnation with the resinous material, is dried under tension at the desired marketable dimensions and the resin is cured while these dimensions are maintained. Such methods are not applicable to knit fabrics, not only because of the differences in construction already mentioned but also because of undesirable efi'ects imparted by such procedure and by the resins heretofore used. The resins which have been applied to woven fabrics and' the amounts of resin generally required to fix the dimensions of woven fabrics are not suitable for knit fabrics. With a hard resin and an appreciable amount of resin deposited on the fabric a hard, boardy hand results which cannot be tolerated in knit garments. But of more serious consequence is the ensuing embrittlement which causes yarns to be broken or cut by needles in fabrication of garments. -While this is of little consequence with woven fabrics, it is disastrous for knit materials as it causes "runs and other defects.
It is an object of this invention to provide a method whereby knitted cellulose fabrics are stabilized against marked changes in dimensions and against distortion. It is an object to accomplish these results without loss of fullness, softness, and required handle and with retention of elasticity, resilience, and normal freeness.
These objects are accomplished by impregnating a knitted cellulose fabric with an aqueous solution containing 8 to 15% of a water-soluble condensate of urea, formaldehyde, and an alcohol, removing excess solution from the fabric to leave 5% to 12% of said condensate in the fabric based on dry weights, spreading the fabric to approximately the desired finished width, drying the spread fabric without tension and heathardening the condensate in the fabric.
The condensates which have been found effective for this process are formed by reacting urea, formaldehyde, and one of the monoor poly-hydric alcohols which in the presence of an acid catalyst react therewithto form water-soluble condensates. The alcohols which yield water-soluble condensates include methyl alcohol, ethyl alcohol, propyl or isopropyl alcohol, ethylene glycol, diethylene glycol, glycerine, dextrose, etc., the polyhydric alcohols yielding particularly effective condensates. If desired, a simple condensate of urea and formaldehyde may first be prepared and then reacted with the hydroxyl-bearing compound. Alternatively the reactants may be directly combined. The reaction.
is carried out in an anhydrous system and water of reaction removed as it is formed. In place of part of the urea there may be used. another carbamide, such as thiourea, or a triazin'e, such the above condensates a small amount of a wetting or penetrating agent. The presence of 1 to 4% of such an agent as octylphenoxyethyl sodium sulfate is, for example, particularly effective in securing thorough penetration of yarns and fibers.
The solution of condensatejmay be applied to the knitted fabric by.dipping,. spraying, orother means suitable for saturating it with'the solution. The wet fabric is then opened out and snread flat preferablmln the case of the usual The tubular knit fabric, by running it over an internal device or shoe which is set to spread the fabric to approximately the finished width which is desired or a slightly wider width. It is then passed between squeeze rolls which express excess solution and which are adjusted to leave only 50% to 80% solution in the fabric. These percentages are based on dry weight of the fabric. When treating cotton fabrics, it is preferable to adjust the concentration of the impregnating solution to between about 8% and 12% of condensate solids and to leave in the cotton only enough condensate to yield from about to about 8% resin after the subsequent treatments, although slightly higher resin contents are sometimes permissible. In the case of knit goods made from rayon or mixtures of cotton. and rayon, however, there may be used solutions with as much as 15% condensate solids and the amount of solution retained may desirably be increased somewhat over that in a cotton fabric, an amount of resin in the final fabric between 6% and 12% being particularly satisfactory.
The spread fabric, free from excess solution,
is then fed into a drier, where it is dried under no tension. A conveyor drier or loop drier is satisfactory for this purpose. Drier temperatures up to 280 F. are usual practice. The dried Example 1 A 16" tubular knit, 5 /2 yd./lb., 305 yarn, cotcontaining 12% urea-formaldehyde glycol condensate, 0.3% of ammonium chloride, and 0.1%
of the sodium salt of octylphenoxyethyl sulfate. The solution was maintained at a temperature of 100 F. The wet fabric was spread to a 17-- inch width o'ver a flat internal shoe. before passcommercial washing machine and dried in a rotating drum-type drier, the shrinkage of the garments was as follows;
Percent Untreated 20 Treated 6 Example 2 A 17 tubular knit, 5 yd./lb. all-spun viscose rayon fabric, peroxide-bleached, scoured, dyed, and dried, was dipped into a solution containing 15% of a urea-formaldehyde-glycol condensate, 0.3% of ammonium thiocyanate and 0.05% sodium octylphenoxyethyl sulfate. The wet fabric was'spread to a width of 18 /2 inches with a flat shoe operating within the tubular fabric, squeezed throug {pair of rolls to leave an 80% ain in weight ased on the dry fabric, and batch-rolled. -'The' fabric was then fed into a carrier drier operating at 250 F. to 260 F. and then into a similar drier operating at 300 F. to heat-harden the condensate.
The resulting fabric exhibited comparatively a small degree of shrinkage, whether tested by home washing methods or in commercial laundry units. The fabric possessed a full hand an resilience without ragginess, and yet was soft and pleasing to the hand.
- Example 3 A 17 /2" tubular knit, spun cuprammonium rayon and cotton mixed fabric, 5 yds./lb., peroxide-bleached, soap-washed, and dried, was
ton fabric, peroxide-bleached, soap-washed, and 5 dried to width, was dipped into a resinsolution ing through a pair of squeez rolls, which removed excess solution from between the fibers and left 60% solution in the fabric. The fabric was then passed without tension through a car-' fabric to pass through this oven. The cured fabric was washed in a. bath containing 0.1%
built soap and 0.1% sodium perborate, rinsed,
squeezed, spread and dried in a carrierdrier.
This fabric was made into garments which were, subjected to wash tests in order to deter-' mine the shrinkage of the resin-containing knit fabric compared to the shrinkage of the usual untreated knit fabric.
solution at 160 F. and air-dried on a clothes line were'found to have shrunk as follows:
- Percent in length Untreated garments 9 Treated garments when other sets of garments werewashedin s Garments washed in a domestic type washing machine with a 0.2% oap v sprayed with a solution. containing 10% of a urea-formaldehyde-glycol condensate, 0.2% of ammonium sulfate, and 0.07% of sodium octylphenoxyethoxyethoxyethyl sulfonate. The fabric was passed through-two sets of rubber brass squeeze rolls, with the final set adjusted to leave an pick-up of solution. After the squeezing operation, the fabric was spread with an internal shoe to a widthof 18%" and passed througha carrierldrier at a temperature of about 260 F. The dry fabric was passed into a loop drier operating at 310 F. where the condensate was cured.
As in the previous examples, the properties of. stability and resistance to change in dimensions of the processed fabric were markedly superior to those of untreated fabric. There was a decreased tendency for stretching and distortion. The hand was greatly improved, the fabric being full and bulky without boardiness. The draping qualities were excellent. Since the sleaziness of the untreated cloth had been eliminated, fabrication of garments was facilitated. There was a decreasein the tendency of runs" to occur.
Example 4 A 27" tubular knit, 3 yds./lb., cotton fabric, peroxide-bleached, dyed with direct dyestuff, soap-washed and dried to width, was spread to a width of 28 inches over a flat internal shoe immediately before being wet outon a slop padder with a solution containing 10% of a water-soluble urea-formaldehyde-ethyl alcohol condensate, 0.2% of ammonium chloride, and 0.1% of the sodium salt of octylphenoxyethyl sulfate. The temperature of the solution was maintained between and F. The wet fabric was then passed through a-set of squeeze rolls, which removed excess solution leaving 80% solution in the goods, based on the dry weight of the fabric.
The cloth was thendried at 260 F. by running aaaacor curing box, which operated at a temperature of 310 F. The cured fabric was then dipped in a solution containing 0.1% of the sodium salt of octylphenoxyethyl sulfate and 0.1% of sodium perborate, spread, squeezed and dried in a carrier-type drier.
The resin-containing fabric when out into garments, exhibited considerably less shrinkage than untreated fabric in garments, whether tested by a commercial laundry procedure or by a home washing procedure. The treated fabric possessed the soft, full hand required for knit goods. There was, furthermore, a marked increase in the washfastness of the direct dyestuif in the treated fabrics.
Heavier fabrics than shown in the above examples may be successfully stabilized by the same general procedure, but with an increase in the time allowed for the steps of penetrating, drying, and curing. When desired, the stabilized fabrics may be treated with softeners, such as sulfonated olive oil, tea-seed oil, castor oil, tallow, etc., or a sulfated long chain aliphatic alcohol, etc., with water-proofing agents, sizing agents or both permanent and non-permanent types, etc. The stabilized fabrics, furthermore, may be subjected to mechanical treatments, such as'preshrinking, with a far greater degree of success than has heretofore been possible.
The process herein described may be successfully applied to knit cellulose fabrics, composed of cotton, or regenerated cellulose, including both viscose and cuprammonia fibers as filaments or staple fibers, or mixtures of these various materials.
We claim:
1. A process for stabilizing knitted cellulose fabric against marked change in dimensions and against distortion of the construction with retention of elasticity, resilience, and freeness of construction which comprises impregnating said fabric with an aqueous solution containing 8 to 15% of a water-soluble condensate of urea, formaldehyde, and an alcohol and a small amount of a strong acid-type catalyst, removing excess solution from the fabric to leave to 12% of said condensate in the fabric, based on dry weights, spreading the fabric to approximatel the desired finished width, drying the spread fabric without tension, and heat-hardening the condensate in the fabric.
2. A process for stabilizing knitted cellulose fabric againstmarked change in dimensions and against distortion of the construction with retention of elasticity, resilience, and freeness of construction which comprises impregnating said fabric with an aqueous solution containing 8 to 15% of a water-soluble condensate of urea, formaldehyde, and ethylene glycol together with a small amount of a strong acid-type catalyst, spreading the impregnated fabric to approximately the-desired finished with, squeezing it to leave therein a condensate content of 5% to 12% based on the weight of the dry fabric, drying the spread fabric without tension, and heat-hardening the condensate in the fabric.
3. A process for stabilizing knitted cellulose fabric against marked change in dimensions and against distortion of the construction with retention of elasticity, resilience, and freeness of construction which comprises impragnating said fabric with an aqueous solution containing 8 to 15% of a water-soluble condensate of urea, formaldehyde and ethylene glycol together with a small amount of an ammonium salt of a strong acid, spreading the impregnated fabric to approximately the desired finished width, squeezing it to leave therein a condensate content of 5% to 12% based on the weight of the dry fabric, drying the spread fabric without tension, and heat-hardening the condensate in the fabric.
4. A process for stabilizing knitted cotton fabric against marked change in dimensions and against distortion of the construction with retention of elasticity, resilience, and freeness of construction which comprises impregnating said fabric with an aqueous solution containing 8 to 12% of a water-soluble condensate of urea, formaldehyde, and ethylene glycol together with a small amount of a strong acid-type catalyst, spreading the impregnated fabric to approximately the desired finished width, squeezing it to leave therein a condensate content of 5 to 8% based on the weight of the dry fabric, drying the spread fabric without tension, and heat-hardening the condensate in the fabric.
5. A process for stabilizing knitted cotton fabric against marked change in dimensions and against distortion of the construction with retention of elasticity, resilience, and freeness ofconstruction which comprises impregnating said fabric with an aqueous solution containing 8 to 12% of a water-soluble condensate of urea, formaldehyde, and a polyhydric alcohol together with a 1 based on the weight of the dry fabric, drying the spread fabric without tension, and heat-harden!- ing the condensate inthe fabric.
6. A process for stabilizing knitted regenerated cellulose fabric against marked change in dimensions and against distortion ofthe construe ,tion with retention of elasticity, resilience, and
freeness of construction which comprises impregnating said fabric with an aqueous solution containing 8 to 15% of a water-soluble condensate of urea, formaldehyde, and ethylene glycol together with a small amount of a strong acid-type catalyst, spreading the impregnated fabric to approximately the desired finished width, squeezing it to leave therein a condensate content of 6 to 12% based on the weight of the dry fabric, drying the spread fabric without tension, and heat-hardening the condensate in the fabric.
7. A process for stabilizing knitted regenerated cellulose fabric against marked change in dimensions and against distortion of theconstruction with retention of elasticity, resilience, and freeness of construction which comprises impregnating said fabric with an aqueous solution containing 8 to 15% of a water-soluble condensate of urea, formaldehyde, and a polyhydric alcohol together with a small amount of a strong acid-type catalyst, spreading the impregnated fabric to approximately the desired finished width, squeezing it to leave therein a condensate content of 6 to 12% based on the weight of the dry fabric, drying the spread fabric without tension, and heat-
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Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2539366A (en) * | 1948-08-12 | 1951-01-23 | American Cyanamid Co | Treatment of wool-containing textile materials |
US2539365A (en) * | 1948-08-12 | 1951-01-23 | American Cyanamid Co | Treatment of wool-containing textile materials |
US2622996A (en) * | 1947-11-28 | 1952-12-23 | Monsanto Chemicals | Treatment of heavy materials comprising keratinous fibers |
US2637662A (en) * | 1950-03-15 | 1953-05-05 | Russell Robert Nicol | Composition and method of its application to cotton glove fabric |
US2662032A (en) * | 1951-08-04 | 1953-12-08 | Us Rubber Co | Process of making a battery separator |
US2859206A (en) * | 1956-07-11 | 1958-11-04 | American Cyanamid Co | Thiourea and urea-formaldehyde mixed resins |
US2881153A (en) * | 1955-03-18 | 1959-04-07 | American Cyanamid Co | Stable thiourea and urea mixed resins and their preparation |
US2881154A (en) * | 1955-03-18 | 1959-04-07 | American Cyanamid Co | Alkylated thiourea-aldehyde resins and their preparation |
US2891019A (en) * | 1954-04-29 | 1959-06-16 | Upson Co | Process for dimensionally stabilizing cellulose and aqueous composition used therefor |
US2922726A (en) * | 1955-03-18 | 1960-01-26 | American Cyanamid Co | Flame-proofing nylon with thiourea containing resin |
US2987418A (en) * | 1956-11-15 | 1961-06-06 | American Cyanamid Co | Non-fibrous regenerated cellulose film carrying modified urea-formaldehyde resin as anchor agent |
US3027247A (en) * | 1957-11-15 | 1962-03-27 | Deering Milliken Res Corp | Buffs and buff fabrics |
US3037262A (en) * | 1961-01-18 | 1962-06-05 | Pepperell Mfg Company | Shed-proof napped blanket fabric |
US3133035A (en) * | 1960-12-09 | 1964-05-12 | Pfersee Chem Fab | Wash resistant finishing means and methods of manufacturing them |
US3148937A (en) * | 1960-06-01 | 1964-09-15 | Fmc Corp | Method of preventing yellowing by nitrogen containing resins cured on cellulose fibers by adding hydrogen peroxide or urea peroxide |
US3191258A (en) * | 1961-12-06 | 1965-06-29 | Pepperell Mfg Company | Method of making shed-proof napped fabric |
US3449228A (en) * | 1965-04-01 | 1969-06-10 | Ppg Industries Inc | Aqueous compositions adapted for electrodeposition |
US3933755A (en) * | 1970-06-02 | 1976-01-20 | Suddeutsche Kalkstickstoff-Werke Ag | Melamine, formaldehyde, thiourea and diol ether thermosetting resin and method of preparing the same |
US3990842A (en) * | 1975-05-15 | 1976-11-09 | Pennwalt Corporation | Ammonium silicofluoride assisted dyeing |
-
1940
- 1940-06-08 US US339591A patent/US2329651A/en not_active Expired - Lifetime
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2622996A (en) * | 1947-11-28 | 1952-12-23 | Monsanto Chemicals | Treatment of heavy materials comprising keratinous fibers |
US2539366A (en) * | 1948-08-12 | 1951-01-23 | American Cyanamid Co | Treatment of wool-containing textile materials |
US2539365A (en) * | 1948-08-12 | 1951-01-23 | American Cyanamid Co | Treatment of wool-containing textile materials |
US2637662A (en) * | 1950-03-15 | 1953-05-05 | Russell Robert Nicol | Composition and method of its application to cotton glove fabric |
US2662032A (en) * | 1951-08-04 | 1953-12-08 | Us Rubber Co | Process of making a battery separator |
US2891019A (en) * | 1954-04-29 | 1959-06-16 | Upson Co | Process for dimensionally stabilizing cellulose and aqueous composition used therefor |
US2881154A (en) * | 1955-03-18 | 1959-04-07 | American Cyanamid Co | Alkylated thiourea-aldehyde resins and their preparation |
US2922726A (en) * | 1955-03-18 | 1960-01-26 | American Cyanamid Co | Flame-proofing nylon with thiourea containing resin |
US2881153A (en) * | 1955-03-18 | 1959-04-07 | American Cyanamid Co | Stable thiourea and urea mixed resins and their preparation |
US2859206A (en) * | 1956-07-11 | 1958-11-04 | American Cyanamid Co | Thiourea and urea-formaldehyde mixed resins |
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