US3871909A - Hosiery finishing process for treating fabrics containing spandex yarn - Google Patents
Hosiery finishing process for treating fabrics containing spandex yarn Download PDFInfo
- Publication number
- US3871909A US3871909A US265318A US26531872A US3871909A US 3871909 A US3871909 A US 3871909A US 265318 A US265318 A US 265318A US 26531872 A US26531872 A US 26531872A US 3871909 A US3871909 A US 3871909A
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- US
- United States
- Prior art keywords
- fabric
- polymer
- bath
- temperature
- urea
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
-
- 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
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
- D06M15/6436—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing amino 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
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31598—Next to silicon-containing [silicone, cement, etc.] layer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31725—Of polyamide
Definitions
- a finishing process for enhancing the wear life and hand of knitted fabrics containing spandex yarn comprises placing the fabric in a bath containing an aqueous emulsion of a polysiloxane polymer, exhausting the polymer onto the surface of the spandex, and adding a curable non-film forming thermosetting resin to the bath under conditions which cause a reaction between the silicone polymer and the resin.
- the present invention relates generally to a method of treating a knitted fabric containing spandex and in particular to an improved finishing process for knitted hosiery including both spandex and nylon yarns.
- spandex which is a long chain synthetic polymer containing approximately 85% or more of segmented polyurethane
- spandex-containing hosiery since spandex is particularly suited to impart elasticity to such knitted fabrics.
- One such hosiery fabric includes a matrix of interconnected spandex yarns with a body of yarn of nylon knitted in a manner to have the requisite stretch and power performance for such stretch or elastic hosiery. More recently, techniques have been developed to impart non-run characteristics to spandex yarns in the fabric at the crossover points.
- a further object of the invention is to provide a finishing process for knitted fabrics including spandex yarns which enhances the surface lubricity of such yarns thereby reducing the rubbery feel or hand normally associated with garments formed from spandexcontaining fabrics.
- a still further object of the invention is to provide a finishing process which enhances the durability of knitted fabrics containing spandex yarns.
- the above and other objects of the invention are accomplished by subjecting knitted fabrics containing spandex yarn to a finishing process whereby the spandex is selectively and sequentially treated with a polysiloxane polymer and a curable thermosetting resin to enhance its surface characteristics.
- the spandex-containing fabric is first exposed to a bath comprising an aqueous emulsion of a polysiloxane polymer having an active hydrogen group and the bath is acidified thereby causing the polymer to exhaust onto the surface of the spandex yarn.
- the time and temperature of the exhaustion step are controlled so as to insure substantial uniformity of absorption on the spandex-containing fabric and to avoid premature cross-linking of the polysiloxane polymer through its active hydrogen prior to the absorption of the polymer into the spandex yarn.
- a curable, non-film forming thermosetting resin and a curing agent or catalyst for the resin are added to the exhausted bath and the bath conditions are controlled so as to promote a relatively uniform reaction between the resin and the absorbed polysiloxane polymer on the surface of the spandex yarn.
- the treated fabric is subjected to elevated temperature for a short period of time in order to cure the reaction product.
- the resulting treated fabrics exhibit a substantially improved hand and enhance durability to wear through repeated launderings as compared to comparable fabrics including untreated spandex yarn.
- the process of the in vention produces a complex molecular structure which becomes permanently attached to the surface of the spandex yarn.
- the molecular structure of spandex yarn permits the absorption of the relatively small polysiloxane molecule into the surface of the spandex yarn and that the more complex molecular structure which is formed as a result of cross-linking between the polysiloxane and the cured thermosetting resin through the active hydrogen on the polysiloxane molecule becomes physically locked within the surface of the spandex.
- the reaction product Due to the physical nature of the polysiloxane and the thermosetting resins employed, the reaction product is an oily or viscous polymer rather than a solid and thereby enhances both the coefficient friction of the treated spandex surface as well as its texture or hand.
- the process of the present invention does not require the use of specialized equipment and may be carried out in conventional hosiery scouring and dyeing equipment upon completion of a conventional dyeing procedure.
- Hosiery dyeing is normally carried out in a paddle or rotary dyeing machine in which the hosiery is bundled together in large bags, the bags are placed in a dye bath and a mechanical action tumbles or moves the bagged hosiery through the bath so as to create a circulation effect which prevents uneven dyeing.
- the bagged hosiery is washed with a mild detergent, rinsed and then dyed.
- the dyeing step is carried out by adding dispersed dyestuffs to a bath and the acidity, temperature of the bath and time are controlled so that the dyes are evenly exhausted onto the hosiery.
- the bagged hosiery is normally rinsed and tumbled dried.
- the finishing procedure contemplated by the present invention may be carried out in the same equipment immediately following the final dye-rinse step.
- any polysiloxane polymer having an active hydrogen may be employed in the finishing process of the invention.
- the following is a general formula for such polymers:
- H H H CH3-Si-0 Si-O S1-CH polysiloxane polymers falling within the above definition are lower alkyl hydrogen polysiloxanes such as methyl or ethyl hydrogen polysiloxane.
- the polysiloxane In order to be useful for the purposes of the present invention, the polysiloxane must be in the form of a water emulsion. Any of the conventional emulsifiers which will maintain a stable water emulsion of polysiloxane until acidifled may be employed. One such preferred emulsifier is tridecyloxypoly (ethyleneoxy)ethanol.
- the curable thermosetting resin which is employed in the finishing process of the invention to form the reaction product on the surface of the spandex should preferably be a non film-forming resin, i.e. it should form a viscous polymer rather than a solid polymer upon curing.
- a preferred thermosetting resin for this purpose is dimethylolethylene urea.
- Other thermosetting resins of this type include glyoxals and carbamates.
- the process of the invention also contemplates the use of a catalyst or curing agent for the resin in the bath.
- a preferred catalyst for this purpose is a zirconium-zinc acetate catalyst.
- Other suitable catalysts include zirconium acetate, zirconium formate and zinc acetate.
- the amounts of silicone emulsion and thermosetting resin which are employed in the process of the invention are not critical. Ordinarily, sufficient amounts of each material will be employed so as to obtain a 2.5 to 4.0 by weight solids concentration on the fabric preferably 3.0 to 3.5 wt.% concentration of the silicone polymer on the finished fabric and a 2.0 to 5.0 wt.% solids concentration, preferably 3.0 to 4.0 wt.% solids concentration of the thermosetting resin on the fabric.
- the amount of catalyst employed is not critical. Ordinarily an amount ranging from 0.2 to 0.5 wt.% of the solids concentration of the catalyst on the fabric will be employed.
- the temperatures, reaction times and specific degree of acidity of the baths employed in carrying out the process are not critical and may be subject to some variation while still achieving the desired result of the process.
- the pH of the bath must be acidic, i.e. less than 7.0 in order to accomplish both the silicone polymer exhaustion step and the subsequent cross-linking reaction.
- the pH can be controlled by the addition of dilute acids such as acetic acid and the pH will be maintained such that the bath is sufficiently acid to permit exhaustion but not so strongly acid as to damage the fabric.
- the exact limits of pH can, of course, be readily determined by experimentation, and it has been found that ordinarily the pH should be maintained between 4.0 and 6.0, preferably 4.0 to 5.0 for both the exhaustion step and the crosslinking reaction.
- the knitted fabric is held in the bath during the silicone exhaustion step for a time sufficient to exhaust substantially all of the silicone polymer in the emulsion onto the spandex yarn.
- the speed at which this exhaustion occurs is a function of both the acidity and temperature of the bath. Obviously, commercial practicality dictates that the exhaustion step be completed in the shortest possible time which will not adversely affect the product and which will permit substantially uniform absorption of the silicone polymer in the spandex yarn.
- the temperature of the bath may be gradually el-v evated from the lowest to the highest temperature of the aforesaid temperature range as the exhaustion proceeds so that uniform absorption occurs in the shortest possible time and cross-linking of the silicone polymer, to the extent which it occurs, occurs subsequent to the absorption of the silicone polymer into the spandex.
- Control of temperature, time and acidity of the exhausted bath after the addition of the curable thermosetting resin and catalyst is generally governed by the same considerations as the silicone polymer exhaustion step.
- the cross-linking reaction will be carried out at the highest temperatures, strongest acidities and for the shortest time which will permit a substantially uniform degree of reaction throughout the fabric.
- the reaction will be permitted to continue at a temperature of to 180F. preferably to F., e.g. 160F.,- for a time sufficient to react substantially all of the resin, e.g. 5 to 15 minutes, preferably 5 to 10 minutes.
- the temperature of the bath may be slowly increased from the lowest to the highest part of the aforesaid temperature range as the reaction proceeds in order to reduce the total required reaction time and to insure a high degree of cross-linking with the'silicone polymer.
- the finishing process of the invention may include appropriate rinsing steps both prior to the silicone exhaustion step and subsequent to the cross-linking reaction step.
- the initial rinse will take place in an aqueous acidic solution which has been acidified with a weak acid such as acetic acid in order to assure uniform acidity throughout the bath and on the fabric so that the silicone polymer will be uniformly exhausted.
- the final rinse may be carried out with water or an aqueous solution of a mild detergent and is included merely for the purpose of removing unreacted materials from the surface of the fabric.
- the knitted fabric or garments are tumbled driedin conventional tumbling equipment which normally includes an extraction step and thereafter are placed in an oven and cured.
- the curing step is carried out at a temperature of 220 to 250F., preferably 220 to 230F., e.g. 230F. for a sufficient time to fully cure the thermosetting resin and the complex molecule formed by cross-linking the thermosetting resin with the silicone polymer, e.g. 5 to 15 minutes, preferably 5 to 7 minutes.
- EXAMPLE 1 Large bags containing knitted hosiery formed from nylon and spandex yarns were placed in a conventional dyeing machine. The bags were scoured in a bath containing tetrasodium pyrophosphate detergent for 15 minutes at 160F. and were then subjected to two successive 5 minute rinses with water at 120F. Thereafter, the hosiery was dyed, using a conventional dye formulation and procedure which included adding the dispersed dyestuffs to the bath and exhausting the dye onto the fabric in a slightly basic medium at elevated temperature. Upon exhaustion of the dye, the bags were rinsed with water at 160F. for 5 minutes.
- the bags of hosiery were left in the dyeing machine and were rinsed with water at a temperature of 120F.
- the pH of the water was adjusted to 5.0 by the addition of acetic acid.
- the bath was dropped and a fresh bath of water adjusted to a pH of 4.5 was circulated for approximately 5 minutes.
- 3 wt.% of a silicone water emulsion containing 3 wt.% silicone polymer solids based upon the weight of the hosiery was added to the bath and the pH was ad justed to 4.0 by the addition of suitable quantities of acetic acid.
- the emulsion comprised methylhydrogen polysiloxane emulsified with tridecyloxypoly(ethyleneoxy) ethanol having a 30 wt.% solids content.
- the temperature of the exhausted bath was dropped to 120F., its pH adjusted to 4.5, and thereafter 0.3 wt.% based on the weight of the hosiery of a zirconiumzinc acetate catalyst and 3 wt.% of dimethylol ethylene urea were added to the bath.
- the bath was circulated for approximately 5 minutes after which time the temperature of the bath was raised to 160F. and held for an additional 5 minutes.
- the bath was then dropped and the bags of hosiery were rinsed with water containing a small amount of soap at a temperature of 110F. for a period of 5 minutes.
- the bags of hosiery were subjected to a conventional drying process consisting of extracting for 2 minutes followed by tumble drying at 200F. for 30 minutes. Finally, the bags of hosiery were placed in a Despatch oven and cured at a temperature of 230F. for 5 minutes.
- the finished hosiery produced in accordance with the above process was subjected to multiple launderings and exhibited significantly more durability than similar hosiery which had not been subjected to the finishing process. Examination of the hosiery revealed that it had an improved hand and did not possess the rubber feel normally associated with the spandexco-ntaining hosiery.
- a finishing process for treating fabrics containing spandex yarn comprising placing the fabric in a bath containing a water emulsion of a lower alkyl polysiloxane polymer, said polymer having an active hydrogen group, acidifying the bath, exhausting said polymer onto said fabric at a temperature of l00 to 200F.
- reaction product is cured by exposure of the fabric to a temperature of 220 to 250F. for a period of 5 to 15 minutes.
- a finishing process for treating fabrics containing spandex yarn comprising placing the fabric in a bath containing a water emulsion of a lower alkyl polysiloxane polymer, said polymer having an active hydrogen group, acidifying the bath, exhausting said polymer onto said fabric at a temperature of 100 to 200F. for a period of 10 to 30 minutes to permit substantially uniform absorption of said polymer by the spandex in said fabric, adding a curabledimethylolethylene urea and a curing agent for said urea to said bath, said urea being curable to form a viscous thermosetting resin, reacting said urea with said absorbed polysiloxane polymer at a temperature of 100 to 180F. for a period of 5 to 15 minutes to permit a substantially uniform reaction throughout the fabric and thereafter subjecting said fabric to a temperature of 220 to 250F. for a period of 5 to 15 minutes to cure the reaction product.
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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)
- Treatment Of Fiber Materials (AREA)
Abstract
Description
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US265318A US3871909A (en) | 1972-06-22 | 1972-06-22 | Hosiery finishing process for treating fabrics containing spandex yarn |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US265318A US3871909A (en) | 1972-06-22 | 1972-06-22 | Hosiery finishing process for treating fabrics containing spandex yarn |
Publications (1)
Publication Number | Publication Date |
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US3871909A true US3871909A (en) | 1975-03-18 |
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Application Number | Title | Priority Date | Filing Date |
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US265318A Expired - Lifetime US3871909A (en) | 1972-06-22 | 1972-06-22 | Hosiery finishing process for treating fabrics containing spandex yarn |
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Country | Link |
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US (1) | US3871909A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3992332A (en) * | 1974-08-22 | 1976-11-16 | Hemson Joseph Zenon | Liquid composition for fabric treatment |
US4169905A (en) * | 1976-11-30 | 1979-10-02 | Rhone-Poulenc Industries | Process for lubricating textile threads |
US4970109A (en) * | 1986-12-12 | 1990-11-13 | Conductex, Inc. | Knitted barrier fabric |
US4978462A (en) * | 1988-09-28 | 1990-12-18 | Dow Corning Limited | Compositions and process for the treatment of textiles comprising a resinous branched polyorganosiloxane and a polydiorganosiloxane in an aqueous dispersion |
US4999120A (en) * | 1990-02-26 | 1991-03-12 | E. I. Du Pont De Nemours And Company | Aqueous emulsion finish for spandex fiber treatment comprising a polydimethyl siloxane and an ethoxylated long-chained alkanol |
US5512319A (en) * | 1994-08-22 | 1996-04-30 | Basf Corporation | Polyurethane foam composite |
CN102140761A (en) * | 2010-11-16 | 2011-08-03 | 辽宁恒星精细化工有限公司 | Cross-linking agent for water coating adhesive of textiles and preparation method therefor |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2785145A (en) * | 1954-07-01 | 1957-03-12 | American Cyanamid Co | Siliconate-aminoplast compositions and textiles coated therewith |
US2881146A (en) * | 1956-07-10 | 1959-04-07 | Du Pont | Organopolysiloxane emulsion containing polymerization catalyst and colloidal silica |
US3293178A (en) * | 1964-02-20 | 1966-12-20 | Arkansas Company Inc | Product and process for rendering pile fabrics soil resistant |
US3296063A (en) * | 1963-11-12 | 1967-01-03 | Du Pont | Synthetic elastomeric lubricated filament |
US3548047A (en) * | 1967-02-23 | 1970-12-15 | Union Carbide Corp | Lubrication of spandex yarns |
US3552908A (en) * | 1969-03-24 | 1971-01-05 | Deering Milliken Res Corp | Dimensionally stabilized elastic fabrics |
US3620821A (en) * | 1968-09-18 | 1971-11-16 | Union Carbide Corp | Treatment of fibers with siloxane-polyoxyalkylene block copolymers containing methoxysiloxy groups |
US3634236A (en) * | 1968-03-20 | 1972-01-11 | Union Carbide Corp | Spandex lubricant composition |
US3677810A (en) * | 1970-09-03 | 1972-07-18 | Dow Corning | Silicone-acrylate soil release treatment for organic textiles |
-
1972
- 1972-06-22 US US265318A patent/US3871909A/en not_active Expired - Lifetime
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2785145A (en) * | 1954-07-01 | 1957-03-12 | American Cyanamid Co | Siliconate-aminoplast compositions and textiles coated therewith |
US2881146A (en) * | 1956-07-10 | 1959-04-07 | Du Pont | Organopolysiloxane emulsion containing polymerization catalyst and colloidal silica |
US3296063A (en) * | 1963-11-12 | 1967-01-03 | Du Pont | Synthetic elastomeric lubricated filament |
US3293178A (en) * | 1964-02-20 | 1966-12-20 | Arkansas Company Inc | Product and process for rendering pile fabrics soil resistant |
US3548047A (en) * | 1967-02-23 | 1970-12-15 | Union Carbide Corp | Lubrication of spandex yarns |
US3634236A (en) * | 1968-03-20 | 1972-01-11 | Union Carbide Corp | Spandex lubricant composition |
US3620821A (en) * | 1968-09-18 | 1971-11-16 | Union Carbide Corp | Treatment of fibers with siloxane-polyoxyalkylene block copolymers containing methoxysiloxy groups |
US3552908A (en) * | 1969-03-24 | 1971-01-05 | Deering Milliken Res Corp | Dimensionally stabilized elastic fabrics |
US3677810A (en) * | 1970-09-03 | 1972-07-18 | Dow Corning | Silicone-acrylate soil release treatment for organic textiles |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3992332A (en) * | 1974-08-22 | 1976-11-16 | Hemson Joseph Zenon | Liquid composition for fabric treatment |
US4169905A (en) * | 1976-11-30 | 1979-10-02 | Rhone-Poulenc Industries | Process for lubricating textile threads |
US4970109A (en) * | 1986-12-12 | 1990-11-13 | Conductex, Inc. | Knitted barrier fabric |
US4978462A (en) * | 1988-09-28 | 1990-12-18 | Dow Corning Limited | Compositions and process for the treatment of textiles comprising a resinous branched polyorganosiloxane and a polydiorganosiloxane in an aqueous dispersion |
US4999120A (en) * | 1990-02-26 | 1991-03-12 | E. I. Du Pont De Nemours And Company | Aqueous emulsion finish for spandex fiber treatment comprising a polydimethyl siloxane and an ethoxylated long-chained alkanol |
US5512319A (en) * | 1994-08-22 | 1996-04-30 | Basf Corporation | Polyurethane foam composite |
CN102140761A (en) * | 2010-11-16 | 2011-08-03 | 辽宁恒星精细化工有限公司 | Cross-linking agent for water coating adhesive of textiles and preparation method therefor |
CN102140761B (en) * | 2010-11-16 | 2012-10-03 | 辽宁恒星精细化工有限公司 | Cross-linking agent for water coating adhesive of textiles and preparation method therefor |
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