US3066107A - Spinning solution comprising viscose and modified polyvinyl alcohol and process for preparing fibers therefrom - Google Patents
Spinning solution comprising viscose and modified polyvinyl alcohol and process for preparing fibers therefrom Download PDFInfo
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- US3066107A US3066107A US27491A US2749160A US3066107A US 3066107 A US3066107 A US 3066107A US 27491 A US27491 A US 27491A US 2749160 A US2749160 A US 2749160A US 3066107 A US3066107 A US 3066107A
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- United States
- Prior art keywords
- polyvinyl alcohol
- viscose
- basic nitrogen
- fibers
- solution
- Prior art date
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- Expired - Lifetime
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- 239000004372 Polyvinyl alcohol Substances 0.000 title claims description 32
- 229920002451 polyvinyl alcohol Polymers 0.000 title claims description 32
- 229920000297 Rayon Polymers 0.000 title claims description 31
- 239000000835 fiber Substances 0.000 title claims description 30
- 238000009987 spinning Methods 0.000 title claims description 24
- 238000004519 manufacturing process Methods 0.000 title description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 66
- 229910052757 nitrogen Inorganic materials 0.000 claims description 33
- 239000010413 mother solution Substances 0.000 claims description 25
- 239000000243 solution Substances 0.000 claims description 24
- 239000004627 regenerated cellulose Substances 0.000 claims description 23
- 239000002245 particle Substances 0.000 claims description 17
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 claims description 15
- 229920002678 cellulose Polymers 0.000 claims description 14
- 239000001913 cellulose Substances 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 11
- 239000004593 Epoxy Substances 0.000 claims description 7
- 239000000047 product Substances 0.000 claims description 7
- 238000006266 etherification reaction Methods 0.000 claims description 6
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 5
- 229920000877 Melamine resin Polymers 0.000 claims description 5
- 238000004043 dyeing Methods 0.000 claims description 5
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 5
- 150000003335 secondary amines Chemical class 0.000 claims description 5
- 150000003973 alkyl amines Chemical class 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical class CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 229940068984 polyvinyl alcohol Drugs 0.000 description 27
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 27
- 229920003043 Cellulose fiber Polymers 0.000 description 17
- 238000000034 method Methods 0.000 description 16
- 239000000843 powder Substances 0.000 description 15
- 239000000975 dye Substances 0.000 description 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 230000008569 process Effects 0.000 description 12
- 238000006359 acetalization reaction Methods 0.000 description 11
- 238000013019 agitation Methods 0.000 description 10
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 239000000980 acid dye Substances 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 8
- 239000004094 surface-active agent Substances 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 7
- 239000000983 mordant dye Substances 0.000 description 7
- -1 non-ionic Chemical group 0.000 description 7
- 239000002270 dispersing agent Substances 0.000 description 6
- 150000001299 aldehydes Chemical class 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000000982 direct dye Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QCOGKXLOEWLIDC-UHFFFAOYSA-N N-methylbutylamine Chemical compound CCCCNC QCOGKXLOEWLIDC-UHFFFAOYSA-N 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- LIWAQLJGPBVORC-UHFFFAOYSA-N ethylmethylamine Chemical compound CCNC LIWAQLJGPBVORC-UHFFFAOYSA-N 0.000 description 2
- 229940015043 glyoxal Drugs 0.000 description 2
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 2
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- FPYUJUBAXZAQNL-UHFFFAOYSA-N 2-chlorobenzaldehyde Chemical compound ClC1=CC=CC=C1C=O FPYUJUBAXZAQNL-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229920000831 ionic polymer Polymers 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- AGVKXDPPPSLISR-UHFFFAOYSA-N n-ethylcyclohexanamine Chemical compound CCNC1CCCCC1 AGVKXDPPPSLISR-UHFFFAOYSA-N 0.000 description 1
- PXSXRABJBXYMFT-UHFFFAOYSA-N n-hexylhexan-1-amine Chemical compound CCCCCCNCCCCCC PXSXRABJBXYMFT-UHFFFAOYSA-N 0.000 description 1
- 150000004002 naphthaldehydes Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- RZFBEFUNINJXRQ-UHFFFAOYSA-M sodium ethyl xanthate Chemical compound [Na+].CCOC([S-])=S RZFBEFUNINJXRQ-UHFFFAOYSA-M 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/08—Cellulose derivatives
- C08L1/22—Cellulose xanthate
- C08L1/24—Viscose
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/909—Polymerization characterized by particle size of product
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/10—Polyvinyl halide esters or alcohol fiber modification
Definitions
- This invention relates to the production of regenerated cellulose fibers and is more particularly concerned with the production of regenerated cellulose fibers of improved dyeing properties.
- the dyeability of regenerated cellulose fibers has been such that only those dyestuffs possessed of an affinity for these fibers, such as direct dyes, sulfide dyes, and the like have been used. More recently, however, it has been desired to spin or Weave regenerated cellulose fibers with fibers which are dyeable not only with direct dyes, but also with acid dyes, or cellitone dyes, such as nylon, cellulose acetate, and the like. There is thus an important need for regenerated cellulose fibers having an improved dyeability with respect to these dyes.
- the process of the present invention is characterized by the fact that spinning of the regenerated cellulose fibers is effected in accordance with well-known procedures from a spinning solution prepared by adding to a conventional regenerated cellulose mother solution water-insoluble polyvinyl-alcohol derivatives in emulsified or powder form which have been produced by etherification of polyvinyl alcohol with epoxy compounds containing basic nitrogen, or ethylene-imine, or their derivatives, and acetalization with an aldehyde containing no basic nitrogen.
- the viscose mother solution has been found to be very stable, although the reason for the stability is not fully understood, when emulsions or powders of water-insoluble polyvinyl-alcohol derivatives of the character described above are added to the viscose mother solution in the quantity needed for the desired improvement in the dyeability of the fibers, this stability being exhibited during the steps of mixing and dispersing, whereby perfect mixing is obtained merely by agitation for a very short time, the dispersion being homogeneous and free from difficulties in handling. There is essentially no difference in the curing or ripening time of the resultant mixed viscose mother solution after the mixing and dispersion of the added polyvinyl alcohol derivative in comparison with the conventional practice wherein viscose alone is employed.
- the content of basic nitrogen in the polymer being more than 0.2%
- the proportion of polymer particles mixed with the viscose mother solution is suitably from about 0.05% to 2% by weight of the cellulose present, measured by the content of the basic nitrogen contained in the polymer.
- an anionic surface-active agent often may form a bond with the basic nitrogen to coagulate the emulsion.
- a non-ionic surface-active agent such as polyoxyethylenedodecyl ether, or a cationic surface-active agent such as dodecyltrimethylammonium chloride.
- water-soluble polymers such as polyvinyl alcohol, partially-saponification products of polyvinyl acetate, gelatin, soluble starch, and amino-acetalized polyvinyl alcohol, are suitably used.
- a non-ionic or cationic polymer be used for the reason referred to in connection with the surface-active agent.
- the regenerated cellulose fibers produced by spinning the mixed viscose mother solution prepared in accordance with this invention can be refined, bleached, and otherwise treated by the same conventional procedures employed in treating regenerated cellulose fibers produced from ordinary viscose mother solutions.
- the viscose mother solutions to which the above-described polyvinyl alcohol derivatives are added in accordance with this invention are those conventionally used in the viscose process for producing fibers of regenerated cellulose.
- the basic nitrogen-containing compounds made use of by the process of this invention are the epoxy compounds obtained by the reaction of epichlorohydrin with secondary amines such as diethyl-amine, dibutyl-amine, dihexylamine, ethyl-cyclohexyl-amine, methyl-butyl-amine, methyl-ethyl-amine, and like alkyl and cycloalkyl amines, and derivatives of compounds having an ethylene-imine ring such as ethylene-imine and compounds obtained by the reaction of ethylene-imine with melamine, and the like.
- secondary amines such as diethyl-amine, dibutyl-amine, dihexylamine, ethyl-cyclohexyl-amine, methyl-butyl-amine, methyl-ethyl-amine, and like alkyl and cycloalkyl amines
- derivatives of compounds having an ethylene-imine ring such as ethylene-imine and compounds obtained by
- the aldehydes used for acetalization are any of the various aliphatic or aromatic aldehydes, or their acetals such as formaldehyde, acetaldehyde, propionaldehyde, butylaldehyde, Z-methyl-hexyl-aldehyde, nonylaldehyde, benzaldehyde, chlorobenzaldehyde, naphthaldehyde, salicylaldehyde, meta-methyl-tetra-hydrobenzaldehyde, glyoxal, and the like commonly employed in the acetalization of polyvinyl alcohol.
- Example I An aqueous solution containing 3% polyvinyl-alcohol (1300 average degree of polymerization), 1% formaldehyde, and 50% sulfuric acid was heated at 50 C. for one hour with agitation by means of an agitator rotating at 1300 r.p.m. The temperature of the solution was then reduced to 40 C., and an aqueous solution containing 0.5% of a dispersant was slowly added drop-wise in a total amount equal to twice the volume of the initial solution, with continued agitation at 1300 r.p.m. As the reaction proceeded, a pure white finely-divided precipitate of polyvinyl-formal was produced. The degree of acetalization of this fine powder was 67%.
- the product thus obtained was a fine powder of a particle size less than 5 in diameter, having very good dyeability, and a basic nitrogen content of 1.5%.
- a spinning solution was then prepared by mixing and dispersing, under agitation, this fine powder in a viscose mother solution made up of 8% cellulose and 6% sodium hydroxide, the amount of powder being selected to provide 0.14% nitrogen based on cellulose in the mixture.
- Example 2 An aqueous solution containing 3% of polyvinyl-alcohol (1500 average degree of polymerization) 1% formaldehyde and 50% sulfuric acid, was heated at 50 C. for 1 hour and a 0.25% water solution of a surface active agent was then added drop-wise very slowly under agitation at the rate of 1500 rpm, in an amount equal in volume to the initial solution.
- the thus-treated solution was then filtered and washed, and polyvinyl-formal in finely-divided form was recovered.
- Ten grams of this polyvinyl-formal were mixed with 2 g. of ethyl-methyl-amino-Z, 3-epoxypropane, and the mixture was heated at 130 C. for 3 hours in a pressure vessel, followed by thorough washing with water and forming the reaction mixture into an emulsion of even finer particle size.
- the diameters of the particles in this emulsion were from 1 to 2 the amount of basic nitrogen 1.2%, and the degree of acetalization 60%.
- This emulsion was then mixed and dispersed under agitation in a viscose mother solution made up of 8% cellulose and 6% sodium hydroxide, making the nitrogen content of the solution 0.1% based on the cellulose.
- This spinning solution was cured and left unattended for 50 hours until the Hotten-Rot value reached 9.5, and spinning was carried out by means of the conventional viscose spinning process.
- the viscose mother solution was observed under the microscope, nothing unusual was observed regarding the diameter and the condition 0 of dispersion of the particles.
- the fiber After spinning, the fiber for 50 hours until its Hotten-Rot value reached 9.5, and
- the fibers produced as described above in accordance with this invention exhibited entirely satisfactory dye absorption with respect to acid dyes, acid mordant dyes, and cellitone dyes.
- the fibers absorbed the dyes almost completely as in the case of the fibers described in Example 1.
- Example 3 An aqueous solution of 3% polyvinyl-alcohol (1000 average degree of polymerization) 4% benzaldehyde, and 20% sulfuric acid was kept at 50 C. for 60 minutes. The particles suspended in the reaction solution were filtered off and thoroughly washed with Warm water at 40 C. The finely-divided particles thus recovered were dried at 60 C. for 20 hours, and then further pulverized to an average diameter of from 2 to 3,u. Ten grams of this fine powder were mixed with 3 g. of ethylene-imine, and the mixture was heated at C. for 3 hours in a pressure vessel. The product was washed after the reaction,
- the amount of basic nitrogen contained in this fine ggigder was 1.5%, and the degree of benzalization was This fine powder was mixed and dispersed with agitation in a viscose mother solution made up of 8% cellulose and 6% sodium hydroxide, making the basic nitrogen content of the solution 0.12% based on the cellulose.
- the spinning solution thus produced was left unattended and cured for 55 hours until the Hotten-Rot value reached 9.5, and was then spun into fibers in the same manner as ordinary viscose.
- the fiber produced by spinning was refined, bleached, and dyed, in conventional manner.
- Example 4 An aqueous solution of 4% of polyvinyl-alcohol (1000 average degree of polymerization), 0.5% formaldehyde, 1% glyoxal, and sulfuric acid was heated at 50 C. for 2 hours under agitation at the rate of 1500 rpm. When the reaction was complete, the finely-divided polyvinylacetal which had formed was separated from the solution by filtration and Was washed, and dried at 60 C.
- a spinning mother solution was prepared by mixing and dispersing this fine powder with agitation in a viscose mother solution made up of 8% cellulose and 6% sodium hydroxide, to provide a nitrogen content of 0.10% based on the cellulose.
- This spinning solution was then cured, after leaving it unattended for 50 hours until a Hotten-Rot value of 9.5 was reached, and was spun into fibers in the same manner as ordinary viscose.
- the nitrogen content of the spun fibers was 0.1% and the spun fibers were refined and bleached in conventional manner.
- the surface-active agents or dispersing agents or dispersants, and protective colloids which are suitably employed are, in addition to those mentioned above, any of the many dispersing agents or dispersants and protective colloids known to those skilled in the art of making emulsions or dispersions of polymers.
- any of the many dispersing agents or dispersants and protective colloids known to those skilled in the art of making emulsions or dispersions of polymers are, for instance, polyoxyethylenedodecyl ether is suitably used as the dispersant.
- a process of producing fibers of regenerated cellulose having improved dyeing properties which comprises the steps of adding to a viscose mother solution water-insoluble polyvinyl alcohol derivatives containing basic nitrogen with a particle size below 30 said derivatives being added in an amount such that the basic nitrogen is 0.05% to 2% by weight of the cellulose present, mixing and dispersing said derivatives in said solution, and spinning said fibers from the resultant spinning solution, said polyvinyl alcohol derivatives being the products obtained by acetalization of polyvinyl alcohol with aldehydes free from basic nitrogen followed by etherification of the resultant acetalized polyvinyl alcohol with a member of the group consisting of epoxy compounds obtained by the reaction of epichlorohydrin with secondary amines selected from the group consisting of alkyl amines and cycloalkyl amines, ethylene-imine, and the reaction product of ethylene-imine with melamine.
- the improvement which comprises adding to a viscose mother solution water-insoluble polyvinyl alcohol derivatives containing basic nitrogen with a particle size below 30a, said derivatives being added in an amount such that the basic nitrogen is 0.05% to 2% by weight of the cellulose present, mixing and dispersing said derivatives in said solution, and spinning said fibers from the resultant spinning solution, said polyvinyl alcohol derivatives being the products obtained by acetalization of polyvinyl alcohol with aldehydes free from basic nitrogen followed by etherification of the resultant acetalized polyvinyl alcohol with a member of the group consisting of epoxy compounds obtained by the reaction of epichlorohydrin with secondary amines selected from the group consisting of alkyl amines and cycloalkyl amines, ethylene-imine, and the reaction product of ethylene-imine with melamine.
- a spinning solution for producing fibers of regenerated cellulose having improved dyeing properties which comprises a viscose mother solution having dispersed therein water-insoluble polyvinyl alcohol derivatives containing basic nitrogen with a particle size of below 30 said derivatives being present in an amount such that the basic nitrogen is 0.05% to 2% by weight of the cellulose present, said polyvinyl alcohol derivatives being the products obtained by acetalization of polyvinyl alcohol with adehydes free from basic nitrogen followed by etherification of the resultant acetalized polyvinyl alcohol with a member of the group consisting of epoxy compounds obtained by the reaction of epichlorohydrin with secondary amines selected from the group consisting of alkyl amines and cycloalkyl amines, ethylene-imine, and the reaction product of ethylene-imine with melamine.
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Polymers & Plastics (AREA)
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- Artificial Filaments (AREA)
Description
United States Patent 3,066,107 SPINNING SOLUTION COMPRISING VISCOSE AND MODIFIED PQLYVINYL ALCQHOL AND PROC- ESS 50R PREPARING FIBERS THEREFROM Osamu Fuknshirna and Hirotoshi Kurashige, Kurashiki City, Japan, assignors to Kurashiki Rayon Co., Ltd., Okayama, Japan, a corporation of Japan No Drawing. Filed May 9, 1960, Bar. No. 27,491 Claims priority, application Japan May 11, 1959 3 Claims. (Cl. 26017.4)
This invention relates to the production of regenerated cellulose fibers and is more particularly concerned with the production of regenerated cellulose fibers of improved dyeing properties.
'Heretofore, the dyeability of regenerated cellulose fibers has been such that only those dyestuffs possessed of an affinity for these fibers, such as direct dyes, sulfide dyes, and the like have been used. More recently, however, it has been desired to spin or Weave regenerated cellulose fibers with fibers which are dyeable not only with direct dyes, but also with acid dyes, or cellitone dyes, such as nylon, cellulose acetate, and the like. There is thus an important need for regenerated cellulose fibers having an improved dyeability with respect to these dyes.
Studies have already been made as revealed bylapanese Patent No. 23 6,202 on a method of mixing high molecular compounds containing basic nitrogen with viscose mother solution for the purpose of improving the dyeability of the regenerated cellulose fibers. In this case, however, since the viscose mother solution is strongly basic, it reacts with cellulose sodium xanthate, producing insoluble precipitates or coagulations during the operations of mixing and dissolving. Therefore, a process of this type wherein the high molecular compounds containing basic nitrogen are xanthogenized beforehand during the dissolving process (Japanese Patent No. 236,202) are required. However, even when such a process is used, it is necessary to efiect curing in a very short time, and to eifect spinning in about one-half the time heretofore employed with regenerated cellulose fibers. For this reason, the stability of the viscose mother solution was very ditficult to maintain under the conditions found in existing industrial installations for handling regenerated cellulose fibers.
It is an object of this invention to provide a process for producing regenerated cellulose fibers having excellent dyeing properties with respect to dyestuffs for which ordinary regenerated cellulose fibers have substantially no affinity, such as acid dyes, acid mordant dyes, and cellitone dyes, the process making it possible to produce fibers by employing substantially the manufacturing methods already known in the production of regenerated cellulose fibers.
As a result of studies directed to a solution of the above-mentioned difliculties, we have discovered that the dyeability of'regenerated cellulose fibers is markedly irnproved with respect to acid dyes, acid mordant dyes, cellitone dyes, and the like, and that no difliculty is encountered in the stability of the mother solution after mixing, and that regenerated cellulose fibers can be spun under well-known manufacturing conditions, when use is made of a spinning mother solution prepared by dispersing, in the viscose mother solution, emulsions or powders of water-insoluble polyvinyl-alcohol derivatives prepared by subjecting polyvinyl alcohol to etherification by means of epoxy compounds, ethylene-imine, or their derivatives containing basic nitrogen, and to acetalization with aldehydes containing no basic nitrogen.
3,fi65,107 Patented Nov. 27, 1962 Thus, the process of the present invention is characterized by the fact that spinning of the regenerated cellulose fibers is effected in accordance with well-known procedures from a spinning solution prepared by adding to a conventional regenerated cellulose mother solution water-insoluble polyvinyl-alcohol derivatives in emulsified or powder form which have been produced by etherification of polyvinyl alcohol with epoxy compounds containing basic nitrogen, or ethylene-imine, or their derivatives, and acetalization with an aldehyde containing no basic nitrogen.
The viscose mother solution has been found to be very stable, although the reason for the stability is not fully understood, when emulsions or powders of water-insoluble polyvinyl-alcohol derivatives of the character described above are added to the viscose mother solution in the quantity needed for the desired improvement in the dyeability of the fibers, this stability being exhibited during the steps of mixing and dispersing, whereby perfect mixing is obtained merely by agitation for a very short time, the dispersion being homogeneous and free from difficulties in handling. There is essentially no difference in the curing or ripening time of the resultant mixed viscose mother solution after the mixing and dispersion of the added polyvinyl alcohol derivative in comparison with the conventional practice wherein viscose alone is employed.
It is advantageous to make the diameter of the particles of the water-insoluble polyvinyl-alcohol derivatives containing basic nitrogen to be mixed and dispersed in the viscose mother solution adequate for the steps of filtration and spinning, viz. less than 30 This invention makes it readily possible to produce particles of from about 0.14-0.17 1. to several tens of ,u, and to mix and disperse particles of desirable diameters. The particle size can be varied to meet the requirements of the mechanical properties and dyeability desired in the fibers in accordance with the fineness of the regenerated celluose fibers manufactured.
The content of basic nitrogen in the polymer being more than 0.2%, the proportion of polymer particles mixed with the viscose mother solution is suitably from about 0.05% to 2% by weight of the cellulose present, measured by the content of the basic nitrogen contained in the polymer. When these proportions are observed, a marked enhancement in the dyeability of the fibers is observed with respect to acid dyes, acid mordant dyes, and cellitone dyes for which heretofore-produced regenerated cellulose fibers have had no aifinity.
In carrying out the acetalization reaction to form the emulsified or powdered polymers suitable for the purpose of this invention, it is generally desirable to employ high speed agitation, and to add various surface-active agents, protective colloids, and the like during the reaction in accordance with conventional emulsification techniques.
In general, various knowmtypes of anionic, non-ionic, and cationic surface-active agents are suitably used. However, an anionic surface-active agent often may form a bond with the basic nitrogen to coagulate the emulsion. Hence, it is preferred to use a non-ionic surface-active agent such as polyoxyethylenedodecyl ether, or a cationic surface-active agent such as dodecyltrimethylammonium chloride. As the protective colloid, water-soluble polymers such as polyvinyl alcohol, partially-saponification products of polyvinyl acetate, gelatin, soluble starch, and amino-acetalized polyvinyl alcohol, are suitably used. In this case, it is also desirable that a non-ionic or cationic polymer be used for the reason referred to in connection with the surface-active agent.
The regenerated cellulose fibers produced by spinning the mixed viscose mother solution prepared in accordance with this invention, can be refined, bleached, and otherwise treated by the same conventional procedures employed in treating regenerated cellulose fibers produced from ordinary viscose mother solutions. The viscose mother solutions to which the above-described polyvinyl alcohol derivatives are added in accordance with this invention are those conventionally used in the viscose process for producing fibers of regenerated cellulose.
The basic nitrogen-containing compounds made use of by the process of this invention are the epoxy compounds obtained by the reaction of epichlorohydrin with secondary amines such as diethyl-amine, dibutyl-amine, dihexylamine, ethyl-cyclohexyl-amine, methyl-butyl-amine, methyl-ethyl-amine, and like alkyl and cycloalkyl amines, and derivatives of compounds having an ethylene-imine ring such as ethylene-imine and compounds obtained by the reaction of ethylene-imine with melamine, and the like.
The aldehydes used for acetalization are any of the various aliphatic or aromatic aldehydes, or their acetals such as formaldehyde, acetaldehyde, propionaldehyde, butylaldehyde, Z-methyl-hexyl-aldehyde, nonylaldehyde, benzaldehyde, chlorobenzaldehyde, naphthaldehyde, salicylaldehyde, meta-methyl-tetra-hydrobenzaldehyde, glyoxal, and the like commonly employed in the acetalization of polyvinyl alcohol.
The invention will be further understood from the following specific examples of practical application. However, it will be understood that these examples are not to be construed as limiting the scope of the present invention in any manner. In these examples, all parts are by weight, unless otherwise indicated.
Example I An aqueous solution containing 3% polyvinyl-alcohol (1300 average degree of polymerization), 1% formaldehyde, and 50% sulfuric acid was heated at 50 C. for one hour with agitation by means of an agitator rotating at 1300 r.p.m. The temperature of the solution was then reduced to 40 C., and an aqueous solution containing 0.5% of a dispersant was slowly added drop-wise in a total amount equal to twice the volume of the initial solution, with continued agitation at 1300 r.p.m. As the reaction proceeded, a pure white finely-divided precipitate of polyvinyl-formal was produced. The degree of acetalization of this fine powder was 67%. The solution was then filtered and the filter cake Washed, and polyvinyl formal in pure white finely divided form was recovered. To 6 g. of this fine powder were added 3 g. of l-dimethylamino-2, 3-epoxypropane, and the mixture was reacted at 120 C. for two hours in a pressure vessel. After the reaction, the finely-divided particles present were separated by filtration and thoroughly washed.
The product thus obtained was a fine powder of a particle size less than 5 in diameter, having very good dyeability, and a basic nitrogen content of 1.5%.
A spinning solution was then prepared by mixing and dispersing, under agitation, this fine powder in a viscose mother solution made up of 8% cellulose and 6% sodium hydroxide, the amount of powder being selected to provide 0.14% nitrogen based on cellulose in the mixture.
This spinning solution was left unattended and cured It was observed that the increase in the amount of dyes absorbed was noticeable in the case of direct dyes, and satisfactory dyeability was manifested with acid dyes, acid mordant dyes, and cellitone dyes. Furthermore, the presence of dyed particles in the fibers after they were dyed was apparent when the fibers were viewed through a microscope.
Example 2 An aqueous solution containing 3% of polyvinyl-alcohol (1500 average degree of polymerization) 1% formaldehyde and 50% sulfuric acid, was heated at 50 C. for 1 hour and a 0.25% water solution of a surface active agent was then added drop-wise very slowly under agitation at the rate of 1500 rpm, in an amount equal in volume to the initial solution.
The thus-treated solution was then filtered and washed, and polyvinyl-formal in finely-divided form was recovered. Ten grams of this polyvinyl-formal were mixed with 2 g. of ethyl-methyl-amino-Z, 3-epoxypropane, and the mixture was heated at 130 C. for 3 hours in a pressure vessel, followed by thorough washing with water and forming the reaction mixture into an emulsion of even finer particle size. The diameters of the particles in this emulsion were from 1 to 2 the amount of basic nitrogen 1.2%, and the degree of acetalization 60%.
This emulsion was then mixed and dispersed under agitation in a viscose mother solution made up of 8% cellulose and 6% sodium hydroxide, making the nitrogen content of the solution 0.1% based on the cellulose.
This spinning solution was cured and left unattended for 50 hours until the Hotten-Rot value reached 9.5, and spinning was carried out by means of the conventional viscose spinning process. When the viscose mother solution was observed under the microscope, nothing unusual was observed regarding the diameter and the condition 0 of dispersion of the particles. After spinning, the fiber for 50 hours until its Hotten-Rot value reached 9.5, and
was refined, bleached, and dyed in accordance with conventional techniques.
The fibers produced as described above in accordance with this invention exhibited entirely satisfactory dye absorption with respect to acid dyes, acid mordant dyes, and cellitone dyes. The fibers absorbed the dyes almost completely as in the case of the fibers described in Example 1.
Example 3 An aqueous solution of 3% polyvinyl-alcohol (1000 average degree of polymerization) 4% benzaldehyde, and 20% sulfuric acid was kept at 50 C. for 60 minutes. The particles suspended in the reaction solution were filtered off and thoroughly washed with Warm water at 40 C. The finely-divided particles thus recovered were dried at 60 C. for 20 hours, and then further pulverized to an average diameter of from 2 to 3,u. Ten grams of this fine powder were mixed with 3 g. of ethylene-imine, and the mixture was heated at C. for 3 hours in a pressure vessel. The product was washed after the reaction,
and a fine powder containing basic nitrogen was obtained.
The amount of basic nitrogen contained in this fine ggigder was 1.5%, and the degree of benzalization was This fine powder was mixed and dispersed with agitation in a viscose mother solution made up of 8% cellulose and 6% sodium hydroxide, making the basic nitrogen content of the solution 0.12% based on the cellulose.
The spinning solution thus produced was left unattended and cured for 55 hours until the Hotten-Rot value reached 9.5, and was then spun into fibers in the same manner as ordinary viscose. The fiber produced by spinning was refined, bleached, and dyed, in conventional manner.
Good results substantially identical with the results described in Example 1 were obtained When these fibers were dyed with direct dyes, acid dyes, acid mordant dyes, and cellitone dyes.
Example 4 An aqueous solution of 4% of polyvinyl-alcohol (1000 average degree of polymerization), 0.5% formaldehyde, 1% glyoxal, and sulfuric acid was heated at 50 C. for 2 hours under agitation at the rate of 1500 rpm. When the reaction was complete, the finely-divided polyvinylacetal which had formed was separated from the solution by filtration and Was washed, and dried at 60 C.
Ten grams of the dried, finely-divided polyvinylacetal were mixed with 3 g. of ethylene-imine, and the mixture was heated at 120 C. for 4 hours in a pressure vessel. After this reaction, the resulting fine powder was thoroughly washed and there was thus obtained a fine powder consisting of polyvinyl acetal containing basic nitrogen. The content of basic nitrogen in this fine powder was 2%, and the degree of acetalization was 60%.
A spinning mother solution was prepared by mixing and dispersing this fine powder with agitation in a viscose mother solution made up of 8% cellulose and 6% sodium hydroxide, to provide a nitrogen content of 0.10% based on the cellulose.
This spinning solution was then cured, after leaving it unattended for 50 hours until a Hotten-Rot value of 9.5 was reached, and was spun into fibers in the same manner as ordinary viscose. The nitrogen content of the spun fibers was 0.1% and the spun fibers were refined and bleached in conventional manner.
Very satisfactory results were obtained when these fibers were dyed not only with direct dyes, but also with acid dyes, acid mordant dyes, and cellitone dyes. The fibers absorbed the dyes ahnost completely.
The surface-active agents or dispersing agents or dispersants, and protective colloids which are suitably employed are, in addition to those mentioned above, any of the many dispersing agents or dispersants and protective colloids known to those skilled in the art of making emulsions or dispersions of polymers. In the foregoing examples, for instance, polyoxyethylenedodecyl ether is suitably used as the dispersant.
It will therefore be understood that, unless otherwise indicated, and as previously mentioned, conventional operations and conventional apparatus are employed in carrying out the process of this invention including conventional mixing and emulsifying units as well as conventional apparatus used in the viscose rayon process. The conditions and the relative relationships set forth in the examples are those preferred in carrying out the process of the invention but it will be understood that other conditions and relationships may be used within the scope of the invention.
It will also be understood that various changes and modifications in addition to those indicated above may be made in the embodiments herein described without departing from the scope of the invention as defined in the appended claims. It is intended, therefore, that all matter contained in the foregoing description shall be interpreted as illustrative only and not as limitative of the invention.
We claim:
1. A process of producing fibers of regenerated cellulose having improved dyeing properties which comprises the steps of adding to a viscose mother solution water-insoluble polyvinyl alcohol derivatives containing basic nitrogen with a particle size below 30 said derivatives being added in an amount such that the basic nitrogen is 0.05% to 2% by weight of the cellulose present, mixing and dispersing said derivatives in said solution, and spinning said fibers from the resultant spinning solution, said polyvinyl alcohol derivatives being the products obtained by acetalization of polyvinyl alcohol with aldehydes free from basic nitrogen followed by etherification of the resultant acetalized polyvinyl alcohol with a member of the group consisting of epoxy compounds obtained by the reaction of epichlorohydrin with secondary amines selected from the group consisting of alkyl amines and cycloalkyl amines, ethylene-imine, and the reaction product of ethylene-imine with melamine.
2. In the production of fibers of regenerated cellulose by the viscose process, the improvement which comprises adding to a viscose mother solution water-insoluble polyvinyl alcohol derivatives containing basic nitrogen with a particle size below 30a, said derivatives being added in an amount such that the basic nitrogen is 0.05% to 2% by weight of the cellulose present, mixing and dispersing said derivatives in said solution, and spinning said fibers from the resultant spinning solution, said polyvinyl alcohol derivatives being the products obtained by acetalization of polyvinyl alcohol with aldehydes free from basic nitrogen followed by etherification of the resultant acetalized polyvinyl alcohol with a member of the group consisting of epoxy compounds obtained by the reaction of epichlorohydrin with secondary amines selected from the group consisting of alkyl amines and cycloalkyl amines, ethylene-imine, and the reaction product of ethylene-imine with melamine.
3. A spinning solution for producing fibers of regenerated cellulose having improved dyeing properties which comprises a viscose mother solution having dispersed therein water-insoluble polyvinyl alcohol derivatives containing basic nitrogen with a particle size of below 30 said derivatives being present in an amount such that the basic nitrogen is 0.05% to 2% by weight of the cellulose present, said polyvinyl alcohol derivatives being the products obtained by acetalization of polyvinyl alcohol with adehydes free from basic nitrogen followed by etherification of the resultant acetalized polyvinyl alcohol with a member of the group consisting of epoxy compounds obtained by the reaction of epichlorohydrin with secondary amines selected from the group consisting of alkyl amines and cycloalkyl amines, ethylene-imine, and the reaction product of ethylene-imine with melamine.
References Cited in the file of this patent UNITED STATES PATENTS 2,092,512 Hermann et al. Sept. 7, 1937 2,906,594 Osugi et al. Sept. 29, 1959
Claims (1)
- 3. A SPINNING SOLUTION FOR PRODUCING FIBERS OF REGENERATED CELLULOSE HAVING IMPROVED DYEING PROPERTIES WHICH COMPRISES A VISCOSE MOTHER SOLUTION HAVING DISPERSED THEREIN WATER-INSOLUBLE POLYVINYL ALCOHOL DERIVATES CONTAINING BASIC NITROGEN WITH A PARTICLE SIZE OF BELOW 30U, SAID DERIVATIVES BEING PRESENT IN AN AMOUNT SUCH THAT THE BASIC NITROGEN IS 0.05% TO 2% BY WEIGHT OF THE CELLULOSE PRESENT, SAID POLYVINYL ALCOHOL DERIVATIVES BEING THE PRODUCTS OBTAINED BY ACETQALIZATION OF POLYVINYL ALCOHOL WITH ADEHYDES FREE FROM BASIC NITROGEN FOLLOWED BY ETHERIFICATION OF THE RESULTANT ACETALIZED POLYVINYL ALCOHOL WITH A MEMBER OF THE GROUP CONSISTING OF EPOXY COMPOUNDS OBTAINED BY THE REACTION OF EPICHLOROHYDRIN WITH SECONDARY AMINES SELECTED FROM THE GROUP CONSISTING OF ALKYL AMINES AND CYCLOALKYL AMINES, ETHYLENE-IMINE, AND THE REACTION PRODUCT OF ETHYLENE-IMINE WITH MELAMINE.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3066107X | 1959-05-11 |
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| US3066107A true US3066107A (en) | 1962-11-27 |
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| US27491A Expired - Lifetime US3066107A (en) | 1959-05-11 | 1960-05-09 | Spinning solution comprising viscose and modified polyvinyl alcohol and process for preparing fibers therefrom |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060134411A1 (en) * | 2004-12-20 | 2006-06-22 | Mackey Larry N | Structures comprising an association agent and processes for making same |
| US20110174041A1 (en) * | 2010-01-15 | 2011-07-21 | Essex Group, Inc. | System for Manufacturing Wire |
| CN102851774A (en) * | 2012-06-06 | 2013-01-02 | 武汉纺织大学 | Method for improving viscose fiber strength |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2092512A (en) * | 1932-10-18 | 1937-09-07 | Chemische Forschungs Gmbh | Reabsorbable threads, bands, tubes, and the like |
| US2906594A (en) * | 1955-12-21 | 1959-09-29 | Air Reduction | Polyvinyl alcohol filaments of improved dye affinity and method of preparation |
-
1960
- 1960-05-09 US US27491A patent/US3066107A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2092512A (en) * | 1932-10-18 | 1937-09-07 | Chemische Forschungs Gmbh | Reabsorbable threads, bands, tubes, and the like |
| US2906594A (en) * | 1955-12-21 | 1959-09-29 | Air Reduction | Polyvinyl alcohol filaments of improved dye affinity and method of preparation |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060134411A1 (en) * | 2004-12-20 | 2006-06-22 | Mackey Larry N | Structures comprising an association agent and processes for making same |
| JP2008523269A (en) * | 2004-12-20 | 2008-07-03 | ザ プロクター アンド ギャンブル カンパニー | Polymer structure containing hydroxyl polymer and method for producing the same |
| US8273453B2 (en) * | 2004-12-20 | 2012-09-25 | The Procter & Gamble Company | Structures comprising an association agent and processes for making same |
| US8343625B2 (en) | 2004-12-20 | 2013-01-01 | The Procter & Gamble Company | Structures comprising an association agent and processes for making same |
| US8715826B2 (en) | 2004-12-20 | 2014-05-06 | The Procter & Gamble Company | Structures comprising an association agent and processes for making same |
| US9297113B2 (en) | 2004-12-20 | 2016-03-29 | The Procter & Gamble Company | Structures comprising an aryl amine and processes for making same |
| US20110174041A1 (en) * | 2010-01-15 | 2011-07-21 | Essex Group, Inc. | System for Manufacturing Wire |
| CN102851774A (en) * | 2012-06-06 | 2013-01-02 | 武汉纺织大学 | Method for improving viscose fiber strength |
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