US3511591A - Process and product of rendering cellulosic fabrics amenable to molding operations - Google Patents
Process and product of rendering cellulosic fabrics amenable to molding operations Download PDFInfo
- Publication number
- US3511591A US3511591A US447098A US3511591DA US3511591A US 3511591 A US3511591 A US 3511591A US 447098 A US447098 A US 447098A US 3511591D A US3511591D A US 3511591DA US 3511591 A US3511591 A US 3511591A
- Authority
- US
- United States
- Prior art keywords
- fabric
- liquid ammonia
- cellulosic
- bath
- minutes
- 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
- 239000004744 fabric Substances 0.000 title description 53
- 238000000034 method Methods 0.000 title description 13
- 238000000465 moulding Methods 0.000 title description 12
- 230000008569 process Effects 0.000 title description 11
- 238000009877 rendering Methods 0.000 title description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 57
- 239000000463 material Substances 0.000 description 47
- 238000012360 testing method Methods 0.000 description 12
- 238000001035 drying Methods 0.000 description 11
- 238000011282 treatment Methods 0.000 description 10
- 239000000123 paper Substances 0.000 description 9
- 239000004753 textile Substances 0.000 description 9
- 239000003112 inhibitor Substances 0.000 description 7
- 230000009471 action Effects 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 238000009864 tensile test Methods 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 229920006266 Vinyl film Polymers 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 5
- 230000006872 improvement Effects 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 229920000297 Rayon Polymers 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- 239000004627 regenerated cellulose Substances 0.000 description 3
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- -1 for instance Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- ZEYUSQVGRCPBPG-UHFFFAOYSA-N 4,5-dihydroxy-1,3-bis(hydroxymethyl)imidazolidin-2-one Chemical compound OCN1C(O)C(O)N(CO)C1=O ZEYUSQVGRCPBPG-UHFFFAOYSA-N 0.000 description 1
- LGJMYGMNWHYGCB-UHFFFAOYSA-N 4,5-dihydroxy-1,3-dimethylimidazolidin-2-one Chemical compound CN1C(O)C(O)N(C)C1=O LGJMYGMNWHYGCB-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- GTTSNKDQDACYLV-UHFFFAOYSA-N Trihydroxybutane Chemical compound CCCC(O)(O)O GTTSNKDQDACYLV-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- WVJOGYWFVNTSAU-UHFFFAOYSA-N dimethylol ethylene urea Chemical compound OCN1CCN(CO)C1=O WVJOGYWFVNTSAU-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- FVGBHSIHHXTYTH-UHFFFAOYSA-N pentane-1,1,1-triol Chemical compound CCCCC(O)(O)O FVGBHSIHHXTYTH-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 235000008790 seltzer Nutrition 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000005406 washing Methods 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/58—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with nitrogen or compounds thereof, e.g. with nitrides
- D06M11/59—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with nitrogen or compounds thereof, e.g. with nitrides with ammonia; with complexes of organic amines with inorganic substances
- D06M11/61—Liquid ammonia
-
- 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
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/02—Natural fibres, other than mineral fibres
- D06M2101/04—Vegetal fibres
- D06M2101/06—Vegetal fibres cellulosic
Definitions
- This invention relates to presensitized cellulosic materials and more specifically to cellulosic materials which are rendered amendable to molding operations.
- Cellulosic materials such as, for instance, paper, regenerated cellulosic films, and knitted and woven textile products composed wholly or partially of cellulosic fibers have been employed in operations which require the cellulosic materials to undergo a considerable degree of deformation.
- the deforming operations are operations such as, for instance, laminating, packaging, and molding and the like.
- cellulosic materials have a certain degree of flexibility, it is found that for certain applications the cellulosic materials have insuflicient strength and flexibility to undergo that degree of deformation which is a prerequisite to the utilization of cellulosic materials.
- Laminates of cellulosic textile materials and vinyl films are to be preferred, for instance, over laminates of thermoplastic textile materials and vinyl films due to the fact that the fabric texture of a cellulosic material does not strike through the vinyl film and the cellulosic material has a high degree of adhesion to the vinyl film.
- the inability of the cellulosic textile materials which have been heretofore known, however, to undergo deformations to which the laminates are subsequently subjected, has severely limited the use of cellulosic textile materials.
- liquid ammonia is preferably maintained at a temperature of from about 60 C. to below about 32 C., the exposure time being for an interval of from about one second to about five minutes.
- the liquid ammonia immersion operation is preferably followed by a 3,511,591 Patented May 12, 1970 drying operation wherein exposure to moisture is minimized.
- the cellulosic material should be a cellulosic material which has been subjected to stresses in its manufacture.
- a stressed cellulosic material may be considered as a material which when not subjected to external mechanical forces is capable of being reduced to a more relaxed state.
- Materials which meet the definition of a stressed cellulosic material are drawn sheets and filaments of cellulosic materials, knitted and woven textile materials, tension calendered paper and the like.
- the stressed cellulosic material should contain in excess of alpha cellulose.
- the treatment converts substantial portions of the cellulosic molecule from a crystalline configuration to an amorphous configuration, the change being readily apparent from a viewing of the X-ray diffractogram before and after liquid ammonia treatment.
- the amorphous structure of the cellulose molecule has been found to be more amenable to conforming to a tortuous configuration than the crystalline structure.
- the amorphous structure is also a structure which may be readily reconverted to the initial crystalline structure.
- a reversion of the cellulosic material from an amorphous structure to a crystalline structure results in the permanent setting of a cellulosic material to that tortuous configuration to which it has conformed itself while in the amorphous state.
- the liquid ammonia treatments also result in a shrinkage of the cellulosic material and a substantial increase in strength.
- the cellulosic material of this invention may be maintained in an amorphous structure for substantial periods of time at temperatures of 25 C. or less, it is preferred to increase the stability of the amorphous structure by impregnation with a bond inhibitor.
- these bond inhibitors fall into two groups which are liquid ammonia compatable polymers and liquid ammonia compatable plasticizers.
- the bond inhibitor may be employed by simply dissolving the inhibitor in the liquid ammonia treating bath.
- Inhibitors which are effective in accordance with this invention are compounds capable of interfering with or substantially preventing the formation of hydrogen bonds between adjacent molecular chains of cellulose.
- the polyhydric alcohols containing 2 to 6 carbon atoms or mixtures thereof have been found to be especially effective and preferably use is made of dihydric and trihydric alcohols exemplified by ethylene glycol, propylene glycol, glycerine, diethanolamine, triethanolamine, trimethylene glycol, butane dioles such as tetramethylene glycol, butane triol, pentane triol, diethylene glycol, dipropylene glycol and triethylene' glycol.
- Polymeric materials which are suitable for use as inhibitors are any of the polymeric materials which are soluble in liquid ammonia as Well as any of the polymeric materials which are soluble in an organic solvent which is soluble in liquid ammonia.
- the term polymeric material as employed herein includes monomeric materials which may be cured in situ to a polymer.
- Polymeric materials which have been found to be especially suitable for purposes of this invention are phenol formaldehyde, melamine formaldehyde, urea formaldehyde, dimethylol ethyleneurea, dihydroxy dimethylol ethyleneurea, polyvinyl alcohol, polyethylene glycol, polyacrylic acid, polyvinl acetate, the sodium salt of styrene-maleic anhydride copolymer and end blocked isocyanate containing polymers.
- the inhibitor is effective over a range of proportions extending from about 5 O to 150 parts by weight, preferably about per 100 parts by weight of cellulose.
- EXAMPLE I A high stretch all cotton knit fabric having a weight of 4.55 yards per pound knitted from singles twenty yarn on an eighteen inch diameter Camber machine so as to have 26 plus or minus 2 wales per inch and 24 plus or minus 2 courses per inch is immersed in a liquid ammonia bath.
- the liquid ammonia bath is maintained at approximately 33 C. and the fabric is subjected to an immersian time in this bath for about 2 minutes.
- the treated fabric is then removed from the bath and passed through a Fleissner drier at the rate of about 1 yard per minute, the rate subjecting the fabric to a total drying time of from about 4 /2 minutes to about minutes.
- the improvement obtained by the liquid ammonia treatment was determined by evaluating an untreated section of the previously identified fabric by means of a Scott Grab Tensile test and then evaluating a treated section in swollen state (area shrinkage-25%) of the previously identified fabric by means of the same test. The results being as follows:
- EXAMPLE III A high stretch jersey knit all rayon fabric having a weight of 4.05 ounces per square yard prepared from singles fifteen viscose rayon staple fiber yarn in a manner so as to have 16.4 wales per inch and 19.2 courses per inch is subjected to a liquid ammonia bath.
- the liquid ammonia bath is maintained at a temperature of about 33 C., the fabric being immersed in the bath for about 2 minutes.
- the fabric is then removed and passed through a Fleissner drier at the rate of about 1 yard per minute, the rate being such to subject the fabric to drying conditions for from about 4 /2 minutes to about 5 minutes.
- the improvement obtained in treating the fabric with liquid ammonia is determined by testing an untreated sample of the previously identified fabric by means of a Scott Grab Tensile test and then repeating the test on a sample of the previously identified fabric which has undergone liquid ammonia treatment, the results being as follows:
- a single jersey stitch paper fabric yarn prepared from paper yarn produced by slitting 10 pound per ream kraft paper to inch width and folding and crimping is subjected to the action of a liquid ammonia bath.
- the paper fabric prior to the liquid ammonia bath treatment is found to have 6 courses per inch and about 4 wales per inch.
- the liquid ammonia bath is maintained at a temperature of about 33 C., the fabric being immersed in a liquid ammonia bath for a period of about 2 minutes.
- the fabric is then removed and passed through a Fleissner drier at a rate of about 1 yard per minute, the rate being suflicient to subject the paper fabric to a drying time for a period of from about 4 /2 minutes to about 5 minutes.
- a sample section of the previously described paper fabric is then subjected to a Scott Grab Tensile test, the test being repeated on a sample section of the previously described paper fabric which has undergone liquid ammonia treatment.
- a comparison of the test results of the Scott Grab Tensile test is found to show an improvement in percent elongation of the liquid ammonia treated fabric over the paper fabric which has not undergone liquid ammonia treatment.
- EXAMPLE V A cotton print cloth having ends and 80 picks per inch prepared from singles forty yarn having a weight for a 39 inch width of 4 yards per pound is subjected to the action of a liquid ammonia bath, the liquid ammonia bath having glycerine dissolved therein in quantities of about 5% by Weight.
- the liquid ammonia bath is maintained at a temperature of about -33 (3., the fabric being immersed in the liquid ammonia bath for a period of about 2 minutes.
- the fabric is then removed and passed through a. Fleissner drier at a rate of about 1 yard per minute, the rate being sufficient to the subject the fabric Scott Grab Tensile Breaking Str. (lbs.)
- EXAMPLE VI A 1 inch by 6 inch sample of untreated regenerated cellulose film having a thickness of .001 inch is immersed in a liquid ammonia bath containing 5% by weight diethylene glycol. The liquid ammonia bath is maintained at approximately 33 C. and the regenerated cellulose film is subjected to an immersion time of about 2 minutes. The ammonia treated film is then removed and allowed to dry at room temperatures under substantially moisture free conditions. The improvement obtained by the liquid ammonia treatment of film was determined by evaluating an untreated 1 inch by 3 inch sample of the previously identified film by placing the lengthwise end of the film in the jaws of an Instron machine. The test was then repeated by placing the ends of the short axis of the sample in the jaws of the Instron machine. Comparable tests were then run on the treated regenerated cellulose film sample with the overall result being as follows:
- a cotton broadcloth of 136 x 64 construction prepared from single thirties fill yarns and single forties warp yarns is subjected to the action of a liquid ammonia bath, the liquid ammonia bath containing 5% based on the weight of the ammonia of dihydroxy dimethyl ethyleneurea.
- the fabric is maintained in the bath for 4 minutes and then removed and immediately molded on a brassiere cup molding device, the mold being maintained at a temperature of 253 F.
- the molded fabric was found to retain its dimensional stability and to be durable to washmg.
- EXAMPLE VIII An all rayon challis fabric of 68 x 62 construction prepared from single thirties rayon staple yarn in both warp and fill directions is immersed for 4 minutes in a liquid ammonia treating bath containing 5% by weight based on the weight of the liquid ammonia of urea formaldehyde. The fabric is then removed and passed through a Fleissner drier at the rate of about 1 yard per minute, the rate being sufiicient to subject the fabric to a drying time for a period of from about 4 /2 minutes to about 5 minutes. The dried fabric is then placed in a brassiere cup mold, the mold being maintained at a temperature of about 253 F. The molded product is found to retain its dimensional stability and to be durable to washing.
- the Scott Grab Tensile test which has been called for in the previous examples is a standard method of tests 6 for breaking load and elongation of textile fabrics and is set forth in ASTM designation D1682-64.
- the Grab test is a test in which only part of the width of the specimen is gripped in the clamps of the testing equipment. For example, in the specimen which is 4 inches and the width of the gripping device 1 inch, the
- the Grab method is applicable whenever it is desired to determine the effective strength of the fabric in use, that is the strength of the yarn in specific width together with the additional strength contributed by adjacent yarn.
- the cellulosic materials of this invention lend themselves to molding operations and especially to the molding operations wherein the cellulosic material retains its dimensional stability by itself or as part of a laminate such as, for instance, a cellulosic fabric-vinyl film laminate. Where the cellulosic material is to retain its molded configuration without undergoing laminating operations, it is preferred that the cellulosic material be treated with a liquid ammonia bath containing a thermosetting resin.
- the molding operations may be any of the molding operations well known to the art such as vacuum molding operations and pressure moldmg operations.
- a process for rendering a stressed woven or knit cellulosic fabric amenable to molding operations which comprises immersing said fabric while in a relaxed state in a bath consisting essentially of a thermosetting resin and liquid ammonia maintained at a temperature from about 60 C. to about 30 C. for a period from about A minute to about 4 minutes and drying the ammonia treated fabric under conditions of minimal moisture exposure.
- a stress relieved woven or knit cellulosic fabric prepared according to the process of claim 1.
- a stress relieved woven or knit cellulosic fabric prepared according to the process of claim 3.
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US44709865A | 1965-04-09 | 1965-04-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3511591A true US3511591A (en) | 1970-05-12 |
Family
ID=23774993
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US447098A Expired - Lifetime US3511591A (en) | 1965-04-09 | 1965-04-09 | Process and product of rendering cellulosic fabrics amenable to molding operations |
Country Status (9)
Country | Link |
---|---|
US (1) | US3511591A (en, 2012) |
BE (1) | BE679303A (en, 2012) |
CH (1) | CH474602A (en, 2012) |
DE (1) | DE1594989A1 (en, 2012) |
ES (1) | ES325235A1 (en, 2012) |
GB (1) | GB1141016A (en, 2012) |
LU (1) | LU50857A1 (en, 2012) |
NL (1) | NL6604641A (en, 2012) |
SE (1) | SE335846B (en, 2012) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3905763A (en) * | 1972-03-14 | 1975-09-16 | Omnium De Prospective Ind Sa | Processes for treating polyamides |
US4425131A (en) | 1979-03-05 | 1984-01-10 | Cluett, Peabody & Co., Inc. | Method of improved pile appearance in liquid ammonia treated fabric; pretreatment with crease resistant resin |
US4475917A (en) * | 1981-09-24 | 1984-10-09 | Asahi Kasei Kogyo Kabushiki Kaisha | Process for modifying regenerated cellulose fiber |
US5910279A (en) * | 1996-04-12 | 1999-06-08 | Nisshinbo Industries, Inc. | Method for forming durable creases in cellulosic fiber textile |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2824420B2 (de) * | 1978-06-03 | 1981-05-07 | Ivanovskij naučno-issledovatel'skij institut chlopčatobumažnoj promyšlennosti, Ivanovo | Verfahren zur Mercerisierung von Baumwollgarn |
DE4312219C2 (de) * | 1993-04-14 | 2002-05-08 | Thueringisches Inst Textil | Verfahren zur Reduzierung der Fibrillierbarkeit von lösungsgesponnenen Cellulosefasern |
JP3743790B2 (ja) * | 1995-08-18 | 2006-02-08 | シキボウ株式会社 | 改質されたセルロース繊維、その製造方法及び繊維製品 |
DE19639141C1 (de) * | 1996-09-24 | 1998-03-05 | Hans Celler | Verfahren zur Behandlung von Textilgut mit flüssigem Ammoniak sowie Vorrichtung zur Durchführung dieses Verfahrens |
DE19742692A1 (de) * | 1997-09-26 | 1999-04-01 | Rhodia Acetow Ag | Verfahren zur Aktivierung von Polysacchariden |
Citations (11)
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---|---|---|---|---|
BE630310A (en, 2012) * | 1962-04-03 | |||
US1989098A (en) * | 1925-06-20 | 1935-01-29 | Lilienfeld Leon | Manufacture of artificial threads |
US1998551A (en) * | 1931-04-01 | 1935-04-23 | Ig Farbenindustrie Ag | Mercerizing process |
US2211872A (en) * | 1937-09-09 | 1940-08-20 | Celanese Corp | Treatment of textile materials |
US2462927A (en) * | 1943-11-06 | 1949-03-01 | Du Pont | Artificial filaments and yarn |
US2528793A (en) * | 1946-01-26 | 1950-11-07 | Kendall & Co | Cotton felt and method of making the same |
GB841401A (en) * | 1957-01-29 | 1960-07-13 | Spinnfaser Ag | A process for improving the utility and crimping intensity of regenerated cellulose textile fibres |
US2955014A (en) * | 1955-03-04 | 1960-10-04 | Segal Leon | Process of treating native cellulose with a liquid alkylenepolyamine and a textile resin |
US3005728A (en) * | 1956-10-19 | 1961-10-24 | Tee Pak Inc | Cellulosic laminates |
US3145132A (en) * | 1961-08-02 | 1964-08-18 | Kendall & Co | Woven stretchable fabrics |
US3347963A (en) * | 1964-12-28 | 1967-10-17 | Little Inc A | Method of stretch forming rayons |
-
1965
- 1965-04-09 US US447098A patent/US3511591A/en not_active Expired - Lifetime
-
1966
- 1966-04-01 GB GB14628/66A patent/GB1141016A/en not_active Expired
- 1966-04-06 SE SE04688/66A patent/SE335846B/xx unknown
- 1966-04-06 ES ES0325235A patent/ES325235A1/es not_active Expired
- 1966-04-06 DE DE19661594989 patent/DE1594989A1/de active Pending
- 1966-04-06 NL NL6604641A patent/NL6604641A/xx unknown
- 1966-04-07 LU LU50857A patent/LU50857A1/xx unknown
- 1966-04-07 CH CH509266A patent/CH474602A/fr not_active IP Right Cessation
- 1966-04-08 BE BE679303D patent/BE679303A/xx unknown
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1989098A (en) * | 1925-06-20 | 1935-01-29 | Lilienfeld Leon | Manufacture of artificial threads |
US1998551A (en) * | 1931-04-01 | 1935-04-23 | Ig Farbenindustrie Ag | Mercerizing process |
US2211872A (en) * | 1937-09-09 | 1940-08-20 | Celanese Corp | Treatment of textile materials |
US2462927A (en) * | 1943-11-06 | 1949-03-01 | Du Pont | Artificial filaments and yarn |
US2528793A (en) * | 1946-01-26 | 1950-11-07 | Kendall & Co | Cotton felt and method of making the same |
US2955014A (en) * | 1955-03-04 | 1960-10-04 | Segal Leon | Process of treating native cellulose with a liquid alkylenepolyamine and a textile resin |
US3005728A (en) * | 1956-10-19 | 1961-10-24 | Tee Pak Inc | Cellulosic laminates |
GB841401A (en) * | 1957-01-29 | 1960-07-13 | Spinnfaser Ag | A process for improving the utility and crimping intensity of regenerated cellulose textile fibres |
US3145132A (en) * | 1961-08-02 | 1964-08-18 | Kendall & Co | Woven stretchable fabrics |
BE630310A (en, 2012) * | 1962-04-03 | |||
US3347963A (en) * | 1964-12-28 | 1967-10-17 | Little Inc A | Method of stretch forming rayons |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3905763A (en) * | 1972-03-14 | 1975-09-16 | Omnium De Prospective Ind Sa | Processes for treating polyamides |
US4425131A (en) | 1979-03-05 | 1984-01-10 | Cluett, Peabody & Co., Inc. | Method of improved pile appearance in liquid ammonia treated fabric; pretreatment with crease resistant resin |
US4475917A (en) * | 1981-09-24 | 1984-10-09 | Asahi Kasei Kogyo Kabushiki Kaisha | Process for modifying regenerated cellulose fiber |
US5910279A (en) * | 1996-04-12 | 1999-06-08 | Nisshinbo Industries, Inc. | Method for forming durable creases in cellulosic fiber textile |
Also Published As
Publication number | Publication date |
---|---|
CH474602A (fr) | 1969-03-14 |
LU50857A1 (en, 2012) | 1966-06-07 |
DE1594989A1 (de) | 1971-05-27 |
SE335846B (en, 2012) | 1971-06-14 |
ES325235A1 (es) | 1967-01-01 |
GB1141016A (en) | 1969-01-22 |
NL6604641A (en, 2012) | 1966-10-10 |
BE679303A (en, 2012) | 1966-09-16 |
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