US3224182A - Process for production of cross-linked cellulosic yarns - Google Patents
Process for production of cross-linked cellulosic yarns Download PDFInfo
- Publication number
- US3224182A US3224182A US96107A US9610761A US3224182A US 3224182 A US3224182 A US 3224182A US 96107 A US96107 A US 96107A US 9610761 A US9610761 A US 9610761A US 3224182 A US3224182 A US 3224182A
- Authority
- US
- United States
- Prior art keywords
- tow
- yarn
- cross
- yarns
- filaments
- 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
- 238000000034 method Methods 0.000 title claims description 22
- 238000004519 manufacturing process Methods 0.000 title claims description 16
- 239000003431 cross linking reagent Substances 0.000 claims description 22
- 238000001035 drying Methods 0.000 claims description 15
- 229920002678 cellulose Polymers 0.000 claims description 13
- 239000001913 cellulose Substances 0.000 claims description 13
- 239000004744 fabric Substances 0.000 description 24
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 18
- 239000000243 solution Substances 0.000 description 17
- 238000011282 treatment Methods 0.000 description 15
- 239000000463 material Substances 0.000 description 14
- 239000000835 fiber Substances 0.000 description 12
- 229920005989 resin Polymers 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 9
- 239000002243 precursor Substances 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 8
- WVJOGYWFVNTSAU-UHFFFAOYSA-N dimethylol ethylene urea Chemical compound OCN1CCN(CO)C1=O WVJOGYWFVNTSAU-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000003153 chemical reaction reagent Substances 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 5
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- 229920000297 Rayon Polymers 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 239000002964 rayon Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 238000002788 crimping Methods 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 3
- OGFLCDAOVUBIBG-UHFFFAOYSA-N octadecanamide;1,3,5-triazine-2,4,6-triamine Chemical class NC1=NC(N)=NC(N)=N1.CCCCCCCCCCCCCCCCCC(N)=O OGFLCDAOVUBIBG-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 238000010382 chemical cross-linking Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 2
- RTLULCVBFCRQKI-UHFFFAOYSA-N 1-amino-4-[3-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-sulfoanilino]-9,10-dioxoanthracene-2-sulfonic acid Chemical compound C1=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C(S(O)(=O)=O)C=C1NC(C=1)=CC=C(S(O)(=O)=O)C=1NC1=NC(Cl)=NC(Cl)=N1 RTLULCVBFCRQKI-UHFFFAOYSA-N 0.000 description 1
- KEYNXNFBSLKJNI-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]ethanol;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound OCCOCCOCCO.OC(=O)CC(O)(C(O)=O)CC(O)=O KEYNXNFBSLKJNI-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000208202 Linaceae Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- NKLPQNGYXWVELD-UHFFFAOYSA-M coomassie brilliant blue Chemical compound [Na+].C1=CC(OCC)=CC=C1NC1=CC=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=C1 NKLPQNGYXWVELD-UHFFFAOYSA-M 0.000 description 1
- 238000009990 desizing Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000004815 dispersion polymer Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 235000019837 monoammonium phosphate Nutrition 0.000 description 1
- 238000009828 non-uniform distribution Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000009999 singeing Methods 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
-
- 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
- the first type of treatment commonly used consists of applying a synthetic resin precursor which penetrates the fibres to the fabric and then curing the resin precursor to form a water insoluble resin which forms a continuous phase extending through the fibres of the fabric.
- Ureaformaldehyde or melamine-formaldehyde resins are used for this type of treatment.
- the second type of treatment consists in applying a compound such as formaldehyde or dimethylol ethylene urea to the fabric. These compounds chemically react with the cellulose molecules and cross-link them to one another and consequently are often referred to as cross linking agents.
- the third type of treatment consists in applying a polymeric material which forms a water insoluble continuous phase on the fabric together with a cross-linking agent. Unlike the first type of treatment however, the continuous phase does not extend into the fibres of the fabric because the polymeric materials used in the treatment are too large to penetrate them. Such polymeric materials may be referred to as extra-fibre polymers.
- the polymeric materials used in this type of treatment may be initially water soluble and are converted during treatment into a water insoluble state.
- hydroxyl group containing polymers such as polyvinyl alcohol or modified cellulose derivative react with the crosslinking agent and become insoluble.
- These polymers wil also be cross-linked to the cellulose molecules of the fabric.
- Thermosetting resins such as unsaturated polyester resins, or acrylic resins may also be used.
- Dispersions of water insoluble polymers such as vinyl acetate, vinyl stearate copolymers may also be applied.
- threads or yarns are produced by impregnating a continuous cellulose filament tow with a solution containing at least one reagent which undergoes a reaction with the cellulose to modify "ice the elastic properties of the component filaments of the tow, such as a synthetic resin precursor or chemical crosslinking agent or an extra-fibre polymer and chemical crosslinking agent, drying the tow whilst maintaining the filaments in continuous relative movement, which prevents continuing contact between given points on adjacent fibres, and thereafter converting the tow into thread or yarn by conventional methods.
- a solution containing at least one reagent which undergoes a reaction with the cellulose to modify "ice the elastic properties of the component filaments of the tow, such as a synthetic resin precursor or chemical crosslinking agent or an extra-fibre polymer and chemical crosslinking agent drying the tow whilst maintaining the filaments in continuous relative movement, which prevents continuing contact between given points on adjacent fibres, and thereafter converting the tow into thread or yarn by conventional methods.
- the heat applied during the drying of the tow may be sufficient to cure the resin, i.e., to convert the resin precursors into the final resin, or to bring the cross-linking about or convert the extra-fibre polymer to an insoluble condition but if it is not sufficient, additional heating may be applied during the drying stage or the necessary heat for curing may be applied subsequently, e.g., after the thread or yarn has been produced or even after the thread or yarn has been converted into fabric or other finished articles. It is especially desirable to cure the resin or bring about cross-linking after the fabric has been woven when it is desired to apply mechanical effects such as embossing and permanent pleating to the finished fabric.
- the tendency of the fibres to become welded together is further reduced by drying the tow at a temperature which is insufiicient to cure the resin precursor completely, then passing the dried or partly dried tow through a known crimping device, such as a pair of rollers delivering the tow into a stufiing box, before curing the resin precursor.
- the crimp so introduced may be partly or wholly removed by applying tension to the tow during curing or it may be retained by curing the tow in its crimped form. Crimping the tow before curing is specially advantageous when treating filaments of fine denier, and if the crimping is not removed, increased resiliency may be imparted to the ultimate yarns.
- Chemically crimped filaments may be treated with a cross-linking agent by the process of the invention. Crimped yarns are especially suited for use as carpet yarns.
- the continuous relative movement during drying in addition to preventing the fibres welding into groups, also ensures a uniform distribution of the reagent. It may be imparted to the filaments in a variety of ways. For treatment with a resin precursor or extra fibre polymer and a cross-linking agent the maximum possible relative movement should be given.
- a particularly suitable method in these cases is to use a hot fiue drier in which the tow is passed over rollers.
- the tow can also be dried by a hot air current such as in a loop drying machine. This method is particularly suitable for treatment of crimped fibres, where a longitudinal tension on the tow is undesirable.
- the tow may be treated after impregnation and before drying with a surface active material which will produce water repellency such as modified melamine stearamide.
- the conversion of the dried and cured tow into yarn may be carried out by conventional steps including stapling and converting the filament tow into a sliver then converting the sliver into a twisted or untwisted roving, spinning the yarn and then doubling the yarn if necessary.
- steps may be carried out on conventional flax, cotton or worsted type machinery, the staple length being conventional for the type of machinery chosen.
- Such steps may also include adjustment of the moisture content and the use of any conventional processing aids.
- fibre may be treated in the form of a continuous filament rove and then spun into staple fibre yarn on a direct spinner.
- the filaments may also be twisted and wound to form a continuous filament yarn.
- the filaments may of course be blended with other fibres or filaments to form a blended yarn.
- the yarns so produced may be converted into knitted or woven fabrics and such fabrics exhibit improved properties particularly of abrasion resistance and strength when compared with fabrics treated with similar reagents after fabrication.
- the yarns so produced are also particularly suitable as tuft or pile yarns for the manufacture of carpets, because of the high resiliency and abrasion resistance which they exhibit either in the manufacture of carpets or of fabrics.
- the yarns produced in accordance with the invention may of course be employed in association with other yarns not produced in accordance with the invention.
- the fibres may be dyed before or after conversion into yarn or after conversion into fabrics, and when used in the production of fabrics the fabrics may also be treated with the same or similar resin precursors or cross-linking agents.
- Example 1 This example illustrates the use of a synthetic resin precursor.
- a linear ester condensation product is prepared by reacting polyethylene glycol (molecular weight 400), with maleic anhydride in equimolecular amounts by the method described in British specification No. 790,837.
- Mix A is further diluted with water to 6% solids and w./v. of B is added to the diluted A mix together with sufiicient ammonium dihydrogen phosphate catalyst to give a pH of about 3.2 on the fibre after curing.
- a length of tow composed of 18 denier filament is padded through the solution (mangle expression 80%) dried on the hot flue and cured for three minutes at 140 C. on a conventional baking stove. The tow is then stapled and processed into yarn by any of the methods previously described. When woven into carpet the resultant pile has much improved resiliency.
- Example 2 This example illustrates the use of an initially water insoluble extra-fibre polymer and a cross-linking agent.
- a length of rayon tow composed of 3 denier fibre was impregnated with the following solution:
- polyester catalyst 0.5% modified melamine stearamide (BIP Chemicals Limited)
- the polyester catalyst was a triethylene glycol citric acid supplied by British Paints Ltd. under the name Wresinol 11542.
- the material was squeezed, dried, crimped and cured, and processed into yarn by any of the methods previously indicated.
- the yarn subsequently woven into cloth was treated as follows:
- Example 3 This example illustrates the use of a cross-linking agent alone.
- a length of rayon tow composed of 18 denier filament was impregnated with the following solution:
- the material is squeezed, dried on a hot flue drier and cured for 2 minutes at C. by a second passage through the hot flue drier.
- the tow is then processed into yarn by any of the methods already described.
- the resultant yarn is used for carpet manufacture and is resilient, has a Very soft handle and good abrasion resistance.
- Example 4 This example illustrates the use of a thermosetting extra fibre polymer.
- a length of tow composed of 4 /2 denier fibre is impregnated with the following solutions:
- thermosetting acrylic resin dispersion (Primal HA-8, Rohm & Haas) 0.5% modified melamine stearamide 3% polyester catalyst
- the material is squeezed, dried, crimped and cured in the normal way and converted into yarn.
- the resultant material When woven into cloth the resultant material has improved stability and abrasion resistance over cloth treated in the conventional way, and has about the same level of crease recovery. Again a characteristic handle is obtained.
- Example 5 This example illustrates the use of a cross linking agent on chemically crimped filaments.
- a length of rayon tow composed of 18 denier chemically crimped filament is impregnated with the following solution:
- Example 6 This example illustrates the use of an initially water soluble extra fibre polymer.
- a length of rayon tow composed of 18 denier filament is impregnated with the following solution:
- a process for the production of cellulosic yarns which comprises the steps of impregnating a continuous cellulose filament tow with a solution containing a crosslinking agent, drying the tow while maintaining the filaments in continuous relative movement and converting the tow into yarn.
- a process for the production of cellulosic yarns which comprises the steps of impregnating a continuous cellulose filament tow with a solution containing a crosslinking agent selected from the group consisting of formaldehyde and dimethylol ethylene urea, drying the toW while maintaining the filaments in continuous relative movement and converting the tow into yarn.
- a crosslinking agent selected from the group consisting of formaldehyde and dimethylol ethylene urea
- a process for the production of cellulosic yarns which comprises the steps of impregnating a continuous cellulose filament tow with a solution containing both a cross-linking agent selected from the group consisting of formaldehyde and dimethylol ethylene urea and an additional reagent selected from the group consisting of urea and melamine, drying the tow while maintaining the filaments in continuous relative movement and converting the tow into yarn.
- a cross-linking agent selected from the group consisting of formaldehyde and dimethylol ethylene urea
- an additional reagent selected from the group consisting of urea and melamine
- a process for the production of cellulosic yarns which comprises the steps of impregnating a continuous cellulose filament tow with a solution containing both a cross-linking agent selected from the group consisting of formaldehyde and dimethylol ethylene urea and water soluble polyvinyl alcohol, drying the tow while maintaining the filaments in continuous relative movement and converting the tow into yarn 7.
- a cross-linking agent selected from the group consisting of formaldehyde and dimethylol ethylene urea and water soluble polyvinyl alcohol
- a process for the production of cellulosic yarns which comprises the steps of impregnating a continuous cellulose filament tow with a solution containing a crosslinking agent, drying the tow while maintaining the filaments in continuous relative movement by passing the tow through a hot flue drier provided with a series of rollers over which the tow passes, and converting the tow into yarn.
- a process for the production of cellulosic yarns which comprises the steps of impregnating a continuous filament tow with a solution containing a cross-linking agent, drying the tow while maintaining the filaments in continuous relative movement by passing the tow through a loop drier, and converting the tow into yarn.
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)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB10313/60A GB978319A (en) | 1960-03-23 | 1960-03-23 | Improvements relating to regenerated cellulose filaments |
Publications (1)
Publication Number | Publication Date |
---|---|
US3224182A true US3224182A (en) | 1965-12-21 |
Family
ID=9965578
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US96107A Expired - Lifetime US3224182A (en) | 1960-03-23 | 1961-03-16 | Process for production of cross-linked cellulosic yarns |
Country Status (3)
Country | Link |
---|---|
US (1) | US3224182A (enrdf_load_stackoverflow) |
GB (1) | GB978319A (enrdf_load_stackoverflow) |
NL (1) | NL262667A (enrdf_load_stackoverflow) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3337931A (en) * | 1966-06-21 | 1967-08-29 | Dixie Yarns | Method of producing yarns which behave as if thermoplastic |
US3507019A (en) * | 1968-04-10 | 1970-04-21 | Sayama Seisakusho Kk | Method for manufacturing screens for papermaking |
US3664381A (en) * | 1970-05-22 | 1972-05-23 | Du Pont | Press free textile fabric |
US3849155A (en) * | 1971-06-18 | 1974-11-19 | Ciba Geigy Ag | Brightening of polyacrylonitrile wet tow |
US3937672A (en) * | 1972-09-23 | 1976-02-10 | Hoechst Aktiengesellschaft | Process for the manufacture of consolidated shaped structures of cellulose hydrate |
US20120282835A1 (en) * | 2010-01-05 | 2012-11-08 | Manikam Ramaswami | High tear strength flame resistant cotton fabric |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2514187A (en) * | 1945-12-29 | 1950-07-04 | Firestone Tire & Rubber Co | Process of producing uniform low stretch cords |
US2877739A (en) * | 1956-12-07 | 1959-03-17 | West Point Mfg Co | Impregnating apparatus |
US2892219A (en) * | 1953-12-09 | 1959-06-30 | Spinnfaser Ag | Method of fluffing a wet fleece of staple fiber and a device for carrying out same |
US2972220A (en) * | 1955-08-04 | 1961-02-21 | Indian Head Mills Inc | Treatment of fibers |
US2978788A (en) * | 1955-07-13 | 1961-04-11 | Du Pont | Process for treating synthetic yarn |
US3039167A (en) * | 1959-09-02 | 1962-06-19 | Courtaulds North America Inc | Method for improving the properties of fabrics containing cross-linked regenerated cellulose material |
-
0
- NL NL262667D patent/NL262667A/xx unknown
-
1960
- 1960-03-23 GB GB10313/60A patent/GB978319A/en not_active Expired
-
1961
- 1961-03-16 US US96107A patent/US3224182A/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2514187A (en) * | 1945-12-29 | 1950-07-04 | Firestone Tire & Rubber Co | Process of producing uniform low stretch cords |
US2892219A (en) * | 1953-12-09 | 1959-06-30 | Spinnfaser Ag | Method of fluffing a wet fleece of staple fiber and a device for carrying out same |
US2978788A (en) * | 1955-07-13 | 1961-04-11 | Du Pont | Process for treating synthetic yarn |
US2972220A (en) * | 1955-08-04 | 1961-02-21 | Indian Head Mills Inc | Treatment of fibers |
US2877739A (en) * | 1956-12-07 | 1959-03-17 | West Point Mfg Co | Impregnating apparatus |
US3039167A (en) * | 1959-09-02 | 1962-06-19 | Courtaulds North America Inc | Method for improving the properties of fabrics containing cross-linked regenerated cellulose material |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3337931A (en) * | 1966-06-21 | 1967-08-29 | Dixie Yarns | Method of producing yarns which behave as if thermoplastic |
US3507019A (en) * | 1968-04-10 | 1970-04-21 | Sayama Seisakusho Kk | Method for manufacturing screens for papermaking |
US3664381A (en) * | 1970-05-22 | 1972-05-23 | Du Pont | Press free textile fabric |
US3849155A (en) * | 1971-06-18 | 1974-11-19 | Ciba Geigy Ag | Brightening of polyacrylonitrile wet tow |
US3937672A (en) * | 1972-09-23 | 1976-02-10 | Hoechst Aktiengesellschaft | Process for the manufacture of consolidated shaped structures of cellulose hydrate |
US20120282835A1 (en) * | 2010-01-05 | 2012-11-08 | Manikam Ramaswami | High tear strength flame resistant cotton fabric |
US8689413B2 (en) * | 2010-01-05 | 2014-04-08 | Manikam Ramaswami | High tear strength flame resistant cotton fabric |
Also Published As
Publication number | Publication date |
---|---|
NL262667A (enrdf_load_stackoverflow) | |
GB978319A (en) | 1964-12-23 |
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