US3143437A - Treatment of polyacrylonitrile textile materials - Google Patents
Treatment of polyacrylonitrile textile materials Download PDFInfo
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- US3143437A US3143437A US4876A US487660A US3143437A US 3143437 A US3143437 A US 3143437A US 4876 A US4876 A US 4876A US 487660 A US487660 A US 487660A US 3143437 A US3143437 A US 3143437A
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- United States
- Prior art keywords
- textile
- fabric
- polyacrylonitrile
- polymer
- solution
- 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.)
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- 239000004753 textile Substances 0.000 title claims description 37
- 229920002239 polyacrylonitrile Polymers 0.000 title claims description 32
- 238000011282 treatment Methods 0.000 title claims description 14
- 239000000463 material Substances 0.000 title description 2
- 239000004744 fabric Substances 0.000 claims description 35
- 239000007788 liquid Substances 0.000 claims description 28
- 229920000642 polymer Polymers 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 17
- 239000002904 solvent Substances 0.000 claims description 16
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 9
- 238000005470 impregnation Methods 0.000 claims description 9
- 238000001035 drying Methods 0.000 claims description 8
- 229920001169 thermoplastic Polymers 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 30
- 239000011521 glass Substances 0.000 description 7
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 2
- 210000001367 artery Anatomy 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 238000010981 drying operation Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000007493 shaping process Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 241001508691 Martes zibellina Species 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 101100323284 Mus musculus Ankrd27 gene Proteins 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 229930188620 butyrolactone Natural products 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009941 weaving 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
- 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
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/244—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons
-
- 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
- D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
- D06M15/03—Polysaccharides or derivatives thereof
- D06M15/05—Cellulose or derivatives thereof
- D06M15/07—Cellulose esters
-
- 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
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/31—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated nitriles
-
- 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
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/327—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof
- D06M15/333—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof of vinyl acetate; Polyvinylalcohol
Definitions
- polyacrylonitrile textile articles is meant threads, fibres and the like consisting of polymers of which at least 85% is acrylonitrile, and woven, knitted or made-up articles based on these yarns fibres or the like.
- a process for the treatment of polyacrylonitrile textile articles to impart a permanent finish thereto which comprises impregnating the polyacrylonitrile textile articles with a composition consisting of a latent solvent for the said textile and a polymer which is soluble, at least at elevated temperature, in the said latent solvent, said impregnation being effected at a temperature below that at which the textile spontaneously dissolves in said latent solvent, and thereafter drying the impregnated articles at a temperature at least equal to the temperature at which the said textile dissolves in the said latent solvent.
- excess liquid may be removed from the textile, e.g., by centrifuging, before the textile is dried.
- latent solvent used in' this invention is meant a liquid which does not spontaneously dissolve the textile below a certain temperature but does dissolve the textile at higher temperatures. With such a latent solvent it is possible to keep the textile in the latent solvent below the said temperature for at least one hour without modification and then to effect dissolution by simply heating the mass. It is to be noted that solutions thus obtained may remain homogeneous when cooled down, i.e., the textile does not spontaneously dissolve at the lower temperature but may not separate from its solution at higher temperatures when that solution is cooled.
- liquids are, for example, dimethylformamide, dimethylacetamide, dimethylsulphoxide and butyrolactone. Mixtures of such liquids may also be employed.
- the polymer introduced into the said liquid may be of any desired nature; for example, it may be a cellulose derivative or a completely synthetic polymer (e.g., a polyolefine, vinyl polymer or acrylic polymer).
- a soluble polymer containing from 85% to 100% of acrylonitrile and up to 15% of another copolyrnen'sable ethylenically unsaturated monomer is particularly suitable.
- the concentration of the polymer in the latent solvent may vary in accordance with the desired effect. It is generally advantageous for it to be present in fairly low concentration, for example in a concentration between 0.1% and 15%, preferably of from 1% to
- the polymer may be dissolved in the latent solvent by any appropriate means, for example by heating for a quarter of an hour at 80 C.
- the impregnation temperature employed depends upon the nature of the polyacrylonitrile textile and that of the latent solvent employed. It must be lower than the temice perature at which the textile dissolves in the said latent solvent.
- the polyacrylonitrile textile article is immersed in the treatment solution at a temperature below that at which the textile would dissolve in the latent solvent, the excess liquid is removed, for example by centrifuging, and the article is then dried.
- the drying temperature may vary within fairly wide limits and may even without difficulty be higher than C., for example, 130 C.
- the stiffness of the finish obtained will vary in accordance with the concentration of the polymer in the treatment solution employed. It is thus possible to adjust the stiffness of the finish in accordance with the desired effect by varying the concentration of the polymer in the treatment solution.
- the process according to the invention may be combined with a particular shaping operation such as folding, crimping, calendering or embossing, which shaping operation may be carried out before, during or after immersion in the treatment solution, but always before the drying of the finish.
- the finish obtained is permanent in the sense in which that word is applied to textile finishes. For example, it resists all washing, dyeing and even bleaching treatments, and it resists rubbing. If the product dissolved in the finishing liquid is itself a polymer based on acrylonitrile, the articles obtained have maximum homogeneity and possess to the highest degree the stability peculiar to this class of polymers.
- Example I A woven fabric consisting of polyacrylonitrile thread is completely immersed at 20 C. in a previously prepared solution containing 20 g. per litre of polyacrylonitrile in dimethylformamide. In order to obtain good penetration the fabric is left immersed for half an hour. The excess liquid is then removed by centrifuging. The weight of liquid retained is 28%. The article is dried for 2 hours at 60 C. and then for half an hour at C.
- the fabric obtained possess a light-weight permanent finish, but the textile properties of the threads are not modified, as may be seen by determination of their tensile strength.
- the breaking elongations of the threads employed are as follows:
- Example III A tube consisting of Helanca type polyacrylonitrile thread, having an internal diameter of 8 mm. and a length of 1.50 .m., obtained in accordance with the method of copending United States application No. 661,015, filed February 19, 1957, now US. Patent No. 3,011,527, and intended for use as an arterial prosthesis, is pulled on to glass rod having an external diameter of 7.8 mm. and a length of 0.50 m.
- Folds are formed in the tube by drawing it along the rod, the two ends being tied.
- the folds are set by steam treatment for a quarter of an hour at 100 C. and for a quarter of an hour at 120 C.
- the set tube withdrawn from the glass rod has circular pleats and is soft.
- the tube obtained is very firm, While retaining satisfactory flexibility and the necessary porosity. More especially, it can be very readily curved without flattening and is particularly suitable for the replacement of diseased arteries, that is, for the op eration known as heterografting.
- It may be bleached and sterilised with boiling water or by steam treatment without modification of its properties, and behaves in the living organism exactly in the manner of a corresponding untreated prosthesis.
- Example IV A fabric consisting of polyacrylonitrile thread is immersed for half an hour in a solution at C. containing 10 g. per litre of polyacrylonitrile in dimethylsulphoxide. After centrifuging to retain a liquid content of 35%, the fabric is dried for two hours at 60 C. and then for half an hour at 120 C. The fabric obtained has a satisfactory light-weight finish.
- Example V A fabric consisting of polyacrylonitrile thread is immersed in a solution, at 0 C., containing 10 g. per litre of a copolymer consisting of 90% of acrylonitrile and 10% of methyl methacrylate in 'y-butyrolactone. The fabric is left immersed for half an hour and the excess liquid is removed by centrifuging. The weight of liquid retained is 35 The product is dried for two hours at 60 C. and for half an hour at 120 C.
- the fabric obtained has a satisfactory light-weight finish.
- Example VI A tube having an internal diameter of 7.3 mm. woven from Helanca type polyacrylonitrile thread obtained in accordance with the method of copending United States application No. 661,015, filed February 19, 1957, now US. Patent No. 3,011,527, but in which the two highshrinkage polyacrylonitrile threads and four Helanca type polyacrylonitrile threads are alternately introduced as weft yarns in the course of the weaving, is pulled on to a glass rod having a diameter of 6.8 mm. and then steamtreated for 15 minutes at 135 C. to shrink the highshrinkage yarn.
- a tube having small circular pleats due to the shrinkage is obtained, which is dried for 15 minutes at 120 C.
- the effect can be further enhanced by a steam treatment for half an hour at 135 C.
- Example VII A tube consisting of Helanca type polyacrylonitrile thread having an internal diameter of 8 mm. and a length of 1.50 m., obtained in accordance with the method of copending United States application No. 661,015, filed February 19, 1957, now US. Patent No. 3,011,527, is immersed, at 20 C., in a solution containing 5% of polyacrylonitrile in dimethylformamide. The excess liquid is removed by centrifuging to retain a liquid content of 38%. The tube is then pulled on to a glass rod having a diameter of 7.8 mm. and a length of 0.50 m. and drawn together into folds; the two ends are then tied on the rod.
- Drying is then effected for half an hour at 120 C., which is sufiicient to produce both a good drying of the finish and a good setting of the folds.
- the tube obtained is elastic and has good radial firmness. It may, more especially, be very readily curved without flattening and is particularly suitable as a substitute for diseased arteries.
- It may be bleached and sterilised with boiling water or by steam treatment without modification of its properties.
- Example V111 A fabric consisting of polyacrylonitrile thread is immersed at 25 C. in a solution containing 5% of polyvinyl chloride in dimethylformamide. The excess liquid is removed by centrifuging to retain a liquid content of 35%. The fabric is then dried for half an hour at 120 C.
- Example IX A woven fabric consisting of polyacrylonitrile thread is immersed, at 25 C., in a solution containing 5% of secondary cellulose acetate in dimethylformamide.
- the excess liquid is removed so as to retain a liquid content of 38%, and the fabric is then dried for half an hour at 120 C.
- A'good stiff finish is obtained without, however, destroying the porosity of the fabric.
- Example X A woven fabric consisting of polyacrylonitrile thread is immersed for half an hour, at 25 C., in a solution containing 5% of a polyvinyl acetate, having a molecular weight of 33,000, in dimethylformamide.
- the excess liquid is removed so as to retain a liquid content of 35 and the fabric is dried for half an hour at 120 C.
- a process for the treatment of acrylonitrile polymer textile fabrics to impart a permanent finish thereto which comprises subjecting textile fabrics formed of a polymer containing at least of acrylonitrile to impregnation with a solution of a thermoplastic polymer in a liquid at a temperature at which the liquid is a non-solvent for the textile fabrics and drying the textile fabrics at a temperature at which the liquid is a solvent, therefor, thereby coating the fibres of which the fabric is composed with the said thermoplastic polymer.
- the textile fabric is a tube woven of high bulk acrylonitrile polymer thread which is drawn together to form pleats and is held in the pleated form during the drying operation.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Materials For Medical Uses (AREA)
Description
United States Patent C) 3,143,437 TREATMENT OF POLYACRYLONITRILE TEXTILE MATERIALS Jean Baptiste Rosset, Lyon, France, assignor to Crylor, Paris, France, a body corporate of France No Drawing. Filed Jan. 27, 1960, Ser. No. 4,876 Claims priority, application France Feb. 2, 1959 9 Claims. (Cl. 117-1383) This invention relates to the production of a so-called permanent finish on polyacrylonitrile textile articles.
By the expression polyacrylonitrile textile articles is meant threads, fibres and the like consisting of polymers of which at least 85% is acrylonitrile, and woven, knitted or made-up articles based on these yarns fibres or the like.
It is known to produce a hardened finish on synthetic plastic filaments by heating the filaments with a solution having a dissolving action at room temperature, for example by treating cellulose acetate articles with acetone.
It is an object of this invention to provide a method of producing a permanent finish on polyacrylonitrile textile articles.
According to the present invention there is provided a process for the treatment of polyacrylonitrile textile articles to impart a permanent finish thereto which comprises impregnating the polyacrylonitrile textile articles with a composition consisting of a latent solvent for the said textile and a polymer which is soluble, at least at elevated temperature, in the said latent solvent, said impregnation being effected at a temperature below that at which the textile spontaneously dissolves in said latent solvent, and thereafter drying the impregnated articles at a temperature at least equal to the temperature at which the said textile dissolves in the said latent solvent. Optionally excess liquid may be removed from the textile, e.g., by centrifuging, before the textile is dried.
By the term latent solvent used in' this invention is meant a liquid which does not spontaneously dissolve the textile below a certain temperature but does dissolve the textile at higher temperatures. With such a latent solvent it is possible to keep the textile in the latent solvent below the said temperature for at least one hour without modification and then to effect dissolution by simply heating the mass. It is to be noted that solutions thus obtained may remain homogeneous when cooled down, i.e., the textile does not spontaneously dissolve at the lower temperature but may not separate from its solution at higher temperatures when that solution is cooled.
In the case of textiles consisting of an acrylonitrile homopolymer, such liquids are, for example, dimethylformamide, dimethylacetamide, dimethylsulphoxide and butyrolactone. Mixtures of such liquids may also be employed.
The polymer introduced into the said liquid may be of any desired nature; for example, it may be a cellulose derivative or a completely synthetic polymer (e.g., a polyolefine, vinyl polymer or acrylic polymer). A soluble polymer containing from 85% to 100% of acrylonitrile and up to 15% of another copolyrnen'sable ethylenically unsaturated monomer is particularly suitable.
The concentration of the polymer in the latent solvent may vary in accordance with the desired effect. It is generally advantageous for it to be present in fairly low concentration, for example in a concentration between 0.1% and 15%, preferably of from 1% to The polymer may be dissolved in the latent solvent by any appropriate means, for example by heating for a quarter of an hour at 80 C.
The impregnation temperature employed depends upon the nature of the polyacrylonitrile textile and that of the latent solvent employed. It must be lower than the temice perature at which the textile dissolves in the said latent solvent.
In the preferred method of carrying out the present invention, the polyacrylonitrile textile article is immersed in the treatment solution at a temperature below that at which the textile would dissolve in the latent solvent, the excess liquid is removed, for example by centrifuging, and the article is then dried. The drying temperature may vary within fairly wide limits and may even without difficulty be higher than C., for example, 130 C.
The stiffness of the finish obtained will vary in accordance with the concentration of the polymer in the treatment solution employed. It is thus possible to adjust the stiffness of the finish in accordance with the desired effect by varying the concentration of the polymer in the treatment solution. In accordance with the ultimate object, the process according to the invention may be combined with a particular shaping operation such as folding, crimping, calendering or embossing, which shaping operation may be carried out before, during or after immersion in the treatment solution, but always before the drying of the finish.
The finish obtained is permanent in the sense in which that word is applied to textile finishes. For example, it resists all washing, dyeing and even bleaching treatments, and it resists rubbing. If the product dissolved in the finishing liquid is itself a polymer based on acrylonitrile, the articles obtained have maximum homogeneity and possess to the highest degree the stability peculiar to this class of polymers.
The following examples will serve to illustrate the invention. All percentages referred to are by weight.
Example I A woven fabric consisting of polyacrylonitrile thread is completely immersed at 20 C. in a previously prepared solution containing 20 g. per litre of polyacrylonitrile in dimethylformamide. In order to obtain good penetration the fabric is left immersed for half an hour. The excess liquid is then removed by centrifuging. The weight of liquid retained is 28%. The article is dried for 2 hours at 60 C. and then for half an hour at C.
The fabric obtained possess a light-weight permanent finish, but the textile properties of the threads are not modified, as may be seen by determination of their tensile strength. The breaking elongations of the threads employed are as follows:
Untreated Treated fabric fabric Example II fabric. The breaking elongations of the threads are as follows:
Untreated Treated fabric fabric Elongation, Percent:
\Varp 20. l 20. 8 20.9 20.9
Example III A tube consisting of Helanca type polyacrylonitrile thread, having an internal diameter of 8 mm. and a length of 1.50 .m., obtained in accordance with the method of copending United States application No. 661,015, filed February 19, 1957, now US. Patent No. 3,011,527, and intended for use as an arterial prosthesis, is pulled on to glass rod having an external diameter of 7.8 mm. and a length of 0.50 m.
Folds are formed in the tube by drawing it along the rod, the two ends being tied.
The folds are set by steam treatment for a quarter of an hour at 100 C. and for a quarter of an hour at 120 C.
The set tube withdrawn from the glass rod has circular pleats and is soft.
It is immersed at 25 C. in a solution containing 2% of polyacrylonitrile in dimethylformamide and then centrifuged. The weight of liquid retained is 35 After drying for one hour at 120 C., the tube obtained is very firm, While retaining satisfactory flexibility and the necessary porosity. More especially, it can be very readily curved without flattening and is particularly suitable for the replacement of diseased arteries, that is, for the op eration known as heterografting.
It may be bleached and sterilised with boiling water or by steam treatment without modification of its properties, and behaves in the living organism exactly in the manner of a corresponding untreated prosthesis.
Example IV A fabric consisting of polyacrylonitrile thread is immersed for half an hour in a solution at C. containing 10 g. per litre of polyacrylonitrile in dimethylsulphoxide. After centrifuging to retain a liquid content of 35%, the fabric is dried for two hours at 60 C. and then for half an hour at 120 C. The fabric obtained has a satisfactory light-weight finish.
Example V A fabric consisting of polyacrylonitrile thread is immersed in a solution, at 0 C., containing 10 g. per litre of a copolymer consisting of 90% of acrylonitrile and 10% of methyl methacrylate in 'y-butyrolactone. The fabric is left immersed for half an hour and the excess liquid is removed by centrifuging. The weight of liquid retained is 35 The product is dried for two hours at 60 C. and for half an hour at 120 C.
The fabric obtained has a satisfactory light-weight finish.
Example VI A tube having an internal diameter of 7.3 mm. woven from Helanca type polyacrylonitrile thread obtained in accordance with the method of copending United States application No. 661,015, filed February 19, 1957, now US. Patent No. 3,011,527, but in which the two highshrinkage polyacrylonitrile threads and four Helanca type polyacrylonitrile threads are alternately introduced as weft yarns in the course of the weaving, is pulled on to a glass rod having a diameter of 6.8 mm. and then steamtreated for 15 minutes at 135 C. to shrink the highshrinkage yarn.
A tube having small circular pleats due to the shrinkage is obtained, which is dried for 15 minutes at 120 C.
It is immersed in a solution, at 25 C., containing 5% of polyacrylonitrile in dimethylformamide. The tube is then centrifuged to retain a liquid content of 35% The tube is then replaced on the glass rod and longitudinally drawn together into folds. The folds form regularly on the existing small circular pleats. The two ends are tied'on the glass rod.
The assembly is then heated in an oven at 120 C. On removal of the glass rod, a'circularly pleated tube for half an hour is obtained, which is elastic in the longitudinal direction and fairly rigid in the radial direction and which does not flatten when bent.
If desired, the effect can be further enhanced by a steam treatment for half an hour at 135 C.
Example VII A tube consisting of Helanca type polyacrylonitrile thread having an internal diameter of 8 mm. and a length of 1.50 m., obtained in accordance with the method of copending United States application No. 661,015, filed February 19, 1957, now US. Patent No. 3,011,527, is immersed, at 20 C., in a solution containing 5% of polyacrylonitrile in dimethylformamide. The excess liquid is removed by centrifuging to retain a liquid content of 38%. The tube is then pulled on to a glass rod having a diameter of 7.8 mm. and a length of 0.50 m. and drawn together into folds; the two ends are then tied on the rod.
Drying is then effected for half an hour at 120 C., which is sufiicient to produce both a good drying of the finish and a good setting of the folds. The tube obtained is elastic and has good radial firmness. It may, more especially, be very readily curved without flattening and is particularly suitable as a substitute for diseased arteries.
It may be bleached and sterilised with boiling water or by steam treatment without modification of its properties.
Example V111 A fabric consisting of polyacrylonitrile thread is immersed at 25 C. in a solution containing 5% of polyvinyl chloride in dimethylformamide. The excess liquid is removed by centrifuging to retain a liquid content of 35%. The fabric is then dried for half an hour at 120 C.
A good, very resistant finish is obtained.
Example IX A woven fabric consisting of polyacrylonitrile thread is immersed, at 25 C., in a solution containing 5% of secondary cellulose acetate in dimethylformamide.
The excess liquid is removed so as to retain a liquid content of 38%, and the fabric is then dried for half an hour at 120 C.
A'good stiff finish is obtained without, however, destroying the porosity of the fabric.
Example X A woven fabric consisting of polyacrylonitrile thread is immersed for half an hour, at 25 C., in a solution containing 5% of a polyvinyl acetate, having a molecular weight of 33,000, in dimethylformamide.
The excess liquid is removed so as to retain a liquid content of 35 and the fabric is dried for half an hour at 120 C.
A good, stiff, very resistant finish is obtained.
I claim:
1. A process for the treatment of acrylonitrile polymer textile fabrics to impart a permanent finish thereto, which comprises subjecting textile fabrics formed of a polymer containing at least of acrylonitrile to impregnation with a solution of a thermoplastic polymer in a liquid at a temperature at which the liquid is a non-solvent for the textile fabrics and drying the textile fabrics at a temperature at which the liquid is a solvent, therefor, thereby coating the fibres of which the fabric is composed with the said thermoplastic polymer.
2. A process according to claim 1, wherein the textile fabric is subjected to impregnation with a solution in dimethylformamide of a polymer which is soluble in dimethylformamide at least at elevated temperatures.
3. A process according to claim 1, wherein the textile fabric is subjected to impregnation with a solution in 'y-butyrolactone of a polymer which is soluble in 'y-butyrolactone at least at elevated temperatures.
4. A process according to claim 1, wherein the textile fabric is subjected to impregnation with a solution in dimethylsulphoxide of a polymer which is soluble in dimethylsulphoxide at least at elevated temperatures.
5. A process according to claim 2, wherein the said impregnating polymer is also an acrylonitrile polymer containing at least 85% of acrylonitrile and is present in the impregnating solution in a concentration of 0.1 to 15% by weight of the solution, and the impregnated fabric is dried at a temperature above 80 C.
6. A process according to claim 5, wherein the said impregnating polymer is also an acrylonitrile polymer containing at least 85% of acrylonitrile and is present in the impregnating solution in a concentration of 0.1 to 15% by weight of the solution, the impregnation is effected at a temperature of at most 0 C., and the impregnated fabric is dried at a temperature above 20 C.
7. A process according to claim 4, wherein the said impregnating polymer is also an acrylonitrile polymer containing at least 85% of acrylonitrile and is present in the impregnating solution in a concentration of 0.1 to 15% by weight of the solution, the impregnation is effected at a temperature of at most 0 C., and the impregnated fabric is dried at a temperature above 20 C.
8. A process according to claim 1, wherein the textile fabric is formed into a desired configuration in which it is maintained during the drying operation.
9. Process according to claim 8, wherein the textile fabric is a tube woven of high bulk acrylonitrile polymer thread which is drawn together to form pleats and is held in the pleated form during the drying operation.
References Cited in the file of this patent UNITED STATES PATENTS 2,245,708 Patton Mar. 9, 1938 2,302,332 Leekey Nov. 17, 1942 2,404,713 Hautz July 23, 1946 2,628,172 Jennett Feb. 10, 1953 2,649,427 Marvel Aug. 18, 1953 2,686,136 McCellan Aug. 10, 1954 2,787,606 Coover et al Apr. 2, 1957 FOREIGN PATENTS 571,376 Canada Feb. 24, 1959 OTHER REFERENCES Houitz: Orlon Acrylic Fibers, Textile Research Journal, November 1950, pp. 786l.
Claims (1)
1. A PROCESS FOR THE TREATMENT OF ACRYLONITRILE POLYMER TEXTILE FABRICS TO IMPART A PERMANENT FINISH THERETO, WHICH COMPRISES SUBJECTING TEXTILE FABRICS FORMED OF A POLYMER CONTAINING AT LEAST 85% OF ACRYLONITRILE TO IMPREGNATION WITH A SOLUTION OF A THERMOPLASTIC POLYMER IN A LIQUID AT A TEMPERATURE AT WHICH THE LIQUID IS A NON-SOLVENT FOR THE TEXTILE FABRICS AND DRYING THE TEXTILE FABRICS AT A TEMPERATURE AT WHICH THE LIQUID IS A SOLVENT, THEREFOR, THEREBY COATING THE FIBRES OF WHICH THE FABRIC IS COMPOSED WITH THE SAID THERMOPLASTIC POLYMER.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR785543A FR1224889A (en) | 1959-02-02 | 1959-02-02 | Permanent primers on polyacrylonitrile textile articles |
Publications (1)
Publication Number | Publication Date |
---|---|
US3143437A true US3143437A (en) | 1964-08-04 |
Family
ID=8710745
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US4876A Expired - Lifetime US3143437A (en) | 1959-02-02 | 1960-01-27 | Treatment of polyacrylonitrile textile materials |
Country Status (4)
Country | Link |
---|---|
US (1) | US3143437A (en) |
DE (1) | DE1137416B (en) |
FR (1) | FR1224889A (en) |
GB (1) | GB870701A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3303050A (en) * | 1965-06-23 | 1967-02-07 | Du Pont | Textile material comprising an acrylonitrile polymer coated with a terpolymer of an acrylic esterr, a vinyl ester and a cross-linking monomer |
US3357878A (en) * | 1965-10-05 | 1967-12-12 | Kendall & Co | Autogenously-bonded needled nonwoven fabric and method of making same |
US3365354A (en) * | 1963-08-07 | 1968-01-23 | Johnson & Johnson | Overlay sheet and process for making the same |
US3403969A (en) * | 1962-10-29 | 1968-10-01 | Bunzl & Biach Ag Fa | Solvent bonding of fiber fleeces including shock-like heat treatment prior to complete vaporization of solvent |
US3844825A (en) * | 1972-11-30 | 1974-10-29 | American Cyanamid Co | Method of producing an acrylic fiber having an improved touch like animal hair |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2245708A (en) * | 1938-03-09 | 1941-06-17 | Carbide & Carbon Chem Corp | Coating process |
US2302332A (en) * | 1940-04-09 | 1942-11-17 | Du Pont | Coating process |
US2404713A (en) * | 1943-06-23 | 1946-07-23 | Du Pont | Method for preparing polymeric solutions |
US2628172A (en) * | 1950-10-20 | 1953-02-10 | Emhart Mfg Co | Process for preparing a polyethylene dispersion and method of applying same to a polyethylene surface |
US2649427A (en) * | 1949-08-09 | 1953-08-18 | Du Pont | Compositions containing a polymer of acrylonitrile and nu, nu-dimethylacetamide |
US2686136A (en) * | 1951-07-24 | 1954-08-10 | Du Pont | Dyeable resin-modified acrylonitrile trile polymers and method for producing same |
US2787606A (en) * | 1952-10-21 | 1957-04-02 | Eastman Kodak Co | Polymerization of acrylonitrile in the presence of preformed homopolymers |
CA571376A (en) * | 1959-02-24 | W. Stanton George | Process for treating shaped polymeric articles to improve dyeability |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB736973A (en) * | 1952-08-22 | 1955-09-14 | Evans Chemicals Ltd | Composition for use in checking laddering in stockings |
GB760837A (en) * | 1954-04-08 | 1956-11-07 | Coats Ltd J & P | Treatment of strands or threads of synthetic organic filaments |
FR1117087A (en) * | 1955-01-07 | 1956-05-16 | Method for treating stockings and means for implementing this method |
-
1959
- 1959-02-02 FR FR785543A patent/FR1224889A/en not_active Expired
- 1959-12-21 GB GB43392/59A patent/GB870701A/en not_active Expired
-
1960
- 1960-01-27 US US4876A patent/US3143437A/en not_active Expired - Lifetime
- 1960-01-28 DE DEC20665A patent/DE1137416B/en active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA571376A (en) * | 1959-02-24 | W. Stanton George | Process for treating shaped polymeric articles to improve dyeability | |
US2245708A (en) * | 1938-03-09 | 1941-06-17 | Carbide & Carbon Chem Corp | Coating process |
US2302332A (en) * | 1940-04-09 | 1942-11-17 | Du Pont | Coating process |
US2404713A (en) * | 1943-06-23 | 1946-07-23 | Du Pont | Method for preparing polymeric solutions |
US2649427A (en) * | 1949-08-09 | 1953-08-18 | Du Pont | Compositions containing a polymer of acrylonitrile and nu, nu-dimethylacetamide |
US2628172A (en) * | 1950-10-20 | 1953-02-10 | Emhart Mfg Co | Process for preparing a polyethylene dispersion and method of applying same to a polyethylene surface |
US2686136A (en) * | 1951-07-24 | 1954-08-10 | Du Pont | Dyeable resin-modified acrylonitrile trile polymers and method for producing same |
US2787606A (en) * | 1952-10-21 | 1957-04-02 | Eastman Kodak Co | Polymerization of acrylonitrile in the presence of preformed homopolymers |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3403969A (en) * | 1962-10-29 | 1968-10-01 | Bunzl & Biach Ag Fa | Solvent bonding of fiber fleeces including shock-like heat treatment prior to complete vaporization of solvent |
US3365354A (en) * | 1963-08-07 | 1968-01-23 | Johnson & Johnson | Overlay sheet and process for making the same |
US3303050A (en) * | 1965-06-23 | 1967-02-07 | Du Pont | Textile material comprising an acrylonitrile polymer coated with a terpolymer of an acrylic esterr, a vinyl ester and a cross-linking monomer |
US3357878A (en) * | 1965-10-05 | 1967-12-12 | Kendall & Co | Autogenously-bonded needled nonwoven fabric and method of making same |
US3844825A (en) * | 1972-11-30 | 1974-10-29 | American Cyanamid Co | Method of producing an acrylic fiber having an improved touch like animal hair |
Also Published As
Publication number | Publication date |
---|---|
GB870701A (en) | 1961-06-14 |
DE1137416B (en) | 1962-10-04 |
FR1224889A (en) | 1960-06-28 |
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