US3098786A - Paper making process - Google Patents
Paper making process Download PDFInfo
- Publication number
- US3098786A US3098786A US78868A US7886860A US3098786A US 3098786 A US3098786 A US 3098786A US 78868 A US78868 A US 78868A US 7886860 A US7886860 A US 7886860A US 3098786 A US3098786 A US 3098786A
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- US
- United States
- Prior art keywords
- percent
- fibers
- paper
- fiber
- acrylic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 238000000034 method Methods 0.000 title claims description 20
- 230000008569 process Effects 0.000 title claims description 14
- 239000000835 fiber Substances 0.000 claims description 50
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 46
- 229920002972 Acrylic fiber Polymers 0.000 claims description 23
- 230000015572 biosynthetic process Effects 0.000 claims description 21
- 239000007900 aqueous suspension Substances 0.000 claims description 11
- 239000000470 constituent Substances 0.000 claims description 5
- 239000000725 suspension Substances 0.000 claims description 4
- 229920000569 Gum karaya Polymers 0.000 description 29
- 235000010494 karaya gum Nutrition 0.000 description 29
- 241000934878 Sterculia Species 0.000 description 28
- 239000000231 karaya gum Substances 0.000 description 28
- 229940039371 karaya gum Drugs 0.000 description 28
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 229920001577 copolymer Polymers 0.000 description 14
- 239000000178 monomer Substances 0.000 description 13
- 239000006185 dispersion Substances 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 12
- 239000000203 mixture Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 240000001058 Sterculia urens Species 0.000 description 6
- 235000015125 Sterculia urens Nutrition 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000002166 wet spinning Methods 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 238000005189 flocculation Methods 0.000 description 5
- 230000016615 flocculation Effects 0.000 description 5
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical class C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 235000015110 jellies Nutrition 0.000 description 4
- 239000008274 jelly Substances 0.000 description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 239000011550 stock solution Substances 0.000 description 4
- SMTDFMMXJHYDDE-UHFFFAOYSA-N 2-prop-1-enylpyridine Chemical compound CC=CC1=CC=CC=N1 SMTDFMMXJHYDDE-UHFFFAOYSA-N 0.000 description 3
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229920002959 polymer blend Polymers 0.000 description 3
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VOCDJQSAMZARGX-UHFFFAOYSA-N 1-ethenylpyrrolidine-2,5-dione Chemical compound C=CN1C(=O)CCC1=O VOCDJQSAMZARGX-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical class OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 description 1
- GPOGMJLHWQHEGF-UHFFFAOYSA-N 2-chloroethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCl GPOGMJLHWQHEGF-UHFFFAOYSA-N 0.000 description 1
- YBXYCBGDIALKAK-UHFFFAOYSA-N 2-chloroprop-2-enamide Chemical compound NC(=O)C(Cl)=C YBXYCBGDIALKAK-UHFFFAOYSA-N 0.000 description 1
- QQBUHYQVKJQAOB-UHFFFAOYSA-N 2-ethenylfuran Chemical compound C=CC1=CC=CO1 QQBUHYQVKJQAOB-UHFFFAOYSA-N 0.000 description 1
- IGDLZDCWMRPMGL-UHFFFAOYSA-N 2-ethenylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(C=C)C(=O)C2=C1 IGDLZDCWMRPMGL-UHFFFAOYSA-N 0.000 description 1
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000480069 Cochlospermum religiosum Species 0.000 description 1
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000008135 aqueous vehicle Substances 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 230000006196 deacetylation Effects 0.000 description 1
- 238000003381 deacetylation reaction Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000007850 degeneration Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- YPTLFOZCUOHVFO-VOTSOKGWSA-N diethyl (e)-2-methylbut-2-enedioate Chemical compound CCOC(=O)\C=C(/C)C(=O)OCC YPTLFOZCUOHVFO-VOTSOKGWSA-N 0.000 description 1
- YPTLFOZCUOHVFO-SREVYHEPSA-N diethyl (z)-2-methylbut-2-enedioate Chemical compound CCOC(=O)\C=C(\C)C(=O)OCC YPTLFOZCUOHVFO-SREVYHEPSA-N 0.000 description 1
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000000578 dry spinning Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- XJELOQYISYPGDX-UHFFFAOYSA-N ethenyl 2-chloroacetate Chemical compound ClCC(=O)OC=C XJELOQYISYPGDX-UHFFFAOYSA-N 0.000 description 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- -1 heterocyclic amines Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005395 methacrylic acid group Chemical class 0.000 description 1
- LVQPBIMCRZQQBC-UHFFFAOYSA-N methoxymethyl 2-methylprop-2-enoate Chemical compound COCOC(=O)C(C)=C LVQPBIMCRZQQBC-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- VOVZXURTCKPRDQ-CQSZACIVSA-N n-[4-[chloro(difluoro)methoxy]phenyl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-5-(1h-pyrazol-5-yl)pyridine-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=NC=C(C(=O)NC=2C=CC(OC(F)(F)Cl)=CC=2)C=C1C1=CC=NN1 VOVZXURTCKPRDQ-CQSZACIVSA-N 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 238000009828 non-uniform distribution Methods 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H5/00—Special paper or cardboard not otherwise provided for
- D21H5/12—Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials
- D21H5/1254—Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials of fibres which have been treated to improve their dispersion in the paper-making furnish
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H13/00—Pulp or paper, comprising synthetic cellulose or non-cellulose fibres or web-forming material
- D21H13/10—Organic non-cellulose fibres
- D21H13/12—Organic non-cellulose fibres from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H13/18—Polymers of unsaturated acids or derivatives thereof, e.g. polyacrylonitriles
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
- D21H17/24—Polysaccharides
- D21H17/31—Gums
Definitions
- This invention relates generally to the manufacture of paper from pulp comprised essentially of acrylic-type fibers. More precisely, the present invention is concerned with improving the uniformity of fiber distribution in paper products produced from acrylic fibers.
- flocculation causes a non-uniform distribution of fibers in the web, and the paper product produced therefrom manifests not only a mottled, uneven appearance but is also defective in such important physical properties as tear, burst and tensile strength.
- the total concentration of solids present in the furnish may vary widely, for example, over a range of from 0.3 percent by weight or less up to 5 percent or more.
- Gum karaya is a natural product obtained from the plant cochlospermum gossypium and allied botanical species.
- the product in its natural state is not an effective wdispersing agent, but is rendered so by either a complete or partial deacetylation, i.e. by substituting acetyl groups for hydroxyl groups.
- This can be accomplished in the following manner: First, take two parts by weight of the dry gum and form a jelly thereof in 98 parts of water.
- the gum maybe advantageously granulated for this purpose but should not be subjected to excessive grinding because it is susceptible to degeneration by mechanical attrition, and when thus broken down will not satisfactorily form the characteristic karaya jelly.
- this 2 percent karaya jelly On each 100 parts of this 2 percent karaya jelly, add 0.6 part of 26 Baum aqueous ammonia.
- the ammonia is mixed with the water and dispersed gum, preferably by mild rather than vigorous agitation. This effects a gradual change in the jelly over a period of from 2 to 3 hours at room temperature, which converts it into the deacetylated derivative. Best results are attained when freshly prepared deacetylated karaya gum is employed. That is to say, this material is most desirably used on the same day that it is prepared.
- the present invention is primarily directed to the particular problem posed :by acrylic-type fibers when used in paper manufacture, the fibers which may be employed in the present invention are not restricted exclusively thereto. That is, other fibers may be blended with acrylics, such vas those derived from cellulose and other sources.
- acrylic fibers as used herein and in the claims, there is meant those fibers which are formed from polyacrylonitrile or copolymers thereof which contain at least 80 percent acrylonitrile in addition to one or more mono-olefinic monomers copolymerizable therewith. There is also included blended polymers and copolymers in which the blend contains at least 80 percent .acrylonitrile.
- Suitable monoolefinic monomers include acrylic, alpha-chloroacrylic [and methacrylic acids; the acrylates, such as methylmethacrylate, ethylmethacrylate, :butylmethacrylate, methoxymethyl methacrylate, beta-chloroethyl methacrylate, and the corresponding esters of acrylic and alpha-chloroacrylic acids; vinyl chloride, vinyl fluoride, vinyl bromide, vinylidene chloride, l-chloro-l-bromoethylene; methacrylonitrile; .acrylamide and methacrylamide; alphachloroacrylamide 'or monoalkyl substitution products thereof; methyl vinyl ketone; vinyl carboxylates, such as vinyl acetate, vinyl chloro
- the polymer may be a tertiary interpolymer, for example, products obtained by the interpolymerization of acrylonit-rile and two or more of any of the monomers, other than acrylonitrile, enumerated above. More specifically, and preferably, the ternary polymer comprises 'acrylonitrile, methacrylonitrile, and 2-vinylpyridine.
- the ternary polymers preferably contain from 80 to 97 percent of acrylonitrile, from 1 to percent of a vinylpyridine or a l-vinylimidazole, and from 1 to 18 percent of another substance; such as methacrylonitrile or vinyl chloride.
- the blended polymers containing at least 80 percent acrylonitri-le may, for example, comprise a major amount of a polymer (A) containing at least 85 percent acrylonitrile and up to percent of one of the above-named mono-olefinic monomers copolymerizable therewith and a minor amount of a polymer (B) containing one of the vinyl-substituted alkyl pyridine monomers noted above and another of the above-named mono-olefinic monomers or acrylonitrile copolymerized therewith.
- A containing at least 85 percent acrylonitrile and up to percent of one of the above-named mono-olefinic monomers copolymerizable therewith
- B a minor amount of a polymer (B) containing one of the vinyl-substituted alkyl pyridine monomers noted above and another of the above-named mono-olefinic monomers or acrylonitrile copolymerized therewith.
- blended polymer compositions preferably contain from 50 to 98 percent of polymer (A), containing at least percent acrylonitrile and up to 15 percent of another monoolefinic monomer copolymerizable therewith, and from 2 to 50 percent of polymer (B), containing at least 30 percent of a vinyl-substituted alkyl pyridine monomer and up to 70 percent of another mono-olefinic monomer copolymerizable therewith, polymers (A) and (B) being so proportioned that the polymer blend contains from 2 to 15 percent of the vinyl-substituted alkyl pyridine monomer in polymerized form. Fibers made from the justadesoribed copolymer blend unexpectedly have a notably excellent propensity to fibrillate so that a superior paper can be manufactured therefrom.
- acrylic fibers formed from other than wetspinning procedures are not considered useful for papermaking, inasmuch as filaments produced by the latter two methods have little tendency to 'fibrillate under the conditions which are employed in conventional papermaking processes. Consequently, the acrylic fibers contemplated for the purposes of the present invention, are those formed by the so called wet-spinning process wherein a water coagulable solution of polymeric material is extruded through a spinneret and the extruded solution is thereafter coagulated in a precipitating bath to form continuous filaments.
- the following series of runs were made to test the effectiveness of sulfuric acid in accentuating the dispersive power of deacctylated karaya gum with respect to dispersions of acrylic fibers in water.
- the fibers employed in reach of the test samples were obtained by the wet spinning of a copolymer blend comprising 88 percent of one copolymer consisting of 94.6 percent acrylonitrile and 5.4 percent vinyl acetate and 12 percent of another copolymer consistin'g of 50 percent acrylonitrile and 50 percent methylvinyl pyridine.
- the fibers had an average length of one-quarter inch and a denier of 3 per filament.
- Example 1 To a one liter beaker there was added a fiber-mix containing 005 gram of acrylic fiber in 500 ml. of water.
- Example 2 To a second one liter beaker there was added 500 ml. of an aqueous slurry containing 0.05 gram of acrylic fiber and an amount of deacetylated karaya gum constituting 5 percent on the weight of the fiber.
- Example 3 To another one liter beaker there was added 500 ml. of an aqueous slurry containing 0.05 gram of acrylic fiber and an amount of deacetylated karaya gum constituting 10 percent on the weight of the fiber.
- Example 4 To another one liter beaker there was added 500 ml.
- Example 6 To still another liter beaker there was added 500 ml. of an aqueous slurry containing 0.05 gram of acrylic Percent I Percent Example karaya sulfuric Result gum added acid added none flocculation. none D0.
- Example 7 A paper furnish was prepared by dispersing 2.5 grams of fibrillated fibers of the above described type in sufficient water to give a consistency of about 0.03 percent. This furnish was then added to the sheet mold of a noble and wood hand sheet machine. The dispersion was dewatered on a 100 mesh wire screen, and the resulting handsheets were couched from the wires onto standard blotting papers. The handsheets were then pressed on a roller type press, and finally dried between blotters on a steam heated drying drum.
- Example 8 To the sheet mold of a paper handsheet machine partially filled with water, there was first introduced a 0.5 stock solution of freshly prepared deacetylated karaya gum. Thereafter, 2.5 grams of fibrillated acrylic fibers were added. The resulting paper furnish had a karaya gum content of percent on the weight of the fiber and a consistency of about 0.03 percent. Water was removed from the fiber dispersion by means of a 100 mesh wire screen. The resulting handsheets were then passed to standard blotting paper after which they were pressed and finally dried.
- Example9 To the sheet mold of a paper handsheet machine, having been partially filled with water, there was first introduced a 0.5 stock solution of freshly prepared deacetylated karaya gum. Thereafter, 2.5 grams of fibrillated acrylic fiber were added to the mold giving a paper furnish having a consistency of about 0.03 percent with a karaya gum content of about percent on the Weight of the fiber. Water was removed from the dispersion by means of a wire screen. The resulting handsheets were then passed to standard blotting paper after which they were pressed and finally dried.
- Example 10 To the sheet mold of a paper handsheet machine, having been previously partially filled with water, there was first introduced a 0.5 stock solution of freshly prepared deacetylated karaya gum. Thereafter, 2.5 grams of fibrillated acrylic fiber were added to the mold, and finally there was slowly added 3.5 ml. of a l N solution of sulfuric acid. The furnish thus prepared had a consistency of about 0.03 percent, and contained 4 percent karaya gum together with 6.8 percent sulfuric acid based on the weight of the fiber present.
- the resulting handsheets were passed to standard blotting paper after which they were pressed and finally dried.
- Example 1 To the sheet mold of a paper handsheet machine, having been previously partially filled with water, there was first introduced a 0.5 stock solution of freshly prepared deacetylated karaya gum. Thereafter, 2.5 grams of fibrillated acrylic fiber were added to the mold, and finally there was slowly added 3.0 ml. of a l N solution of sulfuric acid. The furnish thus prepared had a consistency of about 0.03 percent, and contained 5 percent karaya gum together with 5.8 percent sulfuric acid based on the Weight of the fiber.
- the resulting handsheets were passed to standard blotting paper after which they were pressed and finally dried.
- Uniformity of sheet formation was objectively measwed in each of the above examples by employing an instrument known as the 'Ihwing-A-lbert formation tester.
- This device utilizes a beam of light and a photo-electric cell for measuring the quality of formation.
- the sample to be measured is moved at high velocity between :a steady light sounce and the photo tube.
- the variation in opacity of the paper which may be due to variations in either thickness or structure, cause a fluctuation in the photo-electric cell current.
- the fluctuations are amplified by means of an amplifier of suitable frequency characteristics, until they are of sufficient magnitude to operate a meter.
- the average steady photocell current is indicated on a second meter. The ratio of the readings of the two meters gives the formation value or number.
- the method of this invention provides a means for maintaining acrylic fibers uniformly dispersed in an aqueous medium by employing small amounts of sulfuric acid in combination with deacetylated karaya gum to attain excellent defiocculation.
- the dispersing power of the karaya gum is so greatly enhanced by the presence of small amounts of sulfuric acid that acrylic fibers can be maintained in the uniform dispersion required for paper formation with from 3 to 20 percent of this dispersing agent based on the weight of the fiber present.
- this could be accomplished only by the use of prohibitive amounts of karaya gum, i. e. from 50 to 100 percent on the weight of the fiber.
- a process for making paper from an aqueous suspension of wet-spun acrylic fiblers the step which comprises first adding, to said suspension after all operations designed to modify the fibrous constituents by mechanical means are completed and prior to the formation of the paper web, from 3, to 20 percent of deacetylated karaya gum and thereafter slowly adding as a further component from 4 to percent of sulfuric acid, all percentages being based on the weight of the fibers present in said aqueous suspension, and finally passing said aqueous suspension to a paper web forming device.
- acrylic fibers have been obtained by the wet-spinning of a polymer blend comprising from 50 to 98 percent of one copolymer consisting of at least 85 percent acrylonitrile and up to percent of another mono-olefinic monomer copolymerizable therewith and from 2 to 50 percent of another copolymer consisting of at least percent of a vinyl-substituted alkyl pyridine and up to 70 percent of another monoolefinic monomer copolymerizable therewith.
- a process for making paper from an aqueous suspension of wet-spun acrylic fibers the step which comprises first adding to said suspension after all operations designed to modify the fibrous constituents by mechanical means are completed and prior to the [formation of the paper web, from 4 to 10 percent of deacetylated karaya gum and thereafter slowly adding as a further component from 5 to 8 percent of sulfuric acid, all percentages being based on the weight of the fibers present in said aqueous suspension,:and finally passing said aqueous suspension to a paper web forming device.
- a stage product in the manufacture of paper from an aqueous suspension of wet-spun acrylic fibers comprising the product obtained by first adding to said suspension after all operations designed to modify the fibrous constituents by mechanical means are completed and prior to the formation of the web, from -3 to 20 percent of deacetylated karaya gum and thereafter slowly adding as a further component from 4 to 10 percent of sulfuric acid, all percentages being based on the weight of the fibers present in said aqueous suspension.
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Description
3 ,098,786 Patented July 23, 1963 ice 3,098,786 PAPER MAKING PROCESS James R. Biles, Decatur, Ala, and Richard R. Holmes, Charlotte, N.C., assignors, by mesne assignments, to Monsanto Chemical Company, a corporation of Delaware No Drawing. Filed Dec. 28, 1960, SerQNo. 78,868 5 Claims. (Cl. 162-157) This invention relates generally to the manufacture of paper from pulp comprised essentially of acrylic-type fibers. More precisely, the present invention is concerned with improving the uniformity of fiber distribution in paper products produced from acrylic fibers.
In the manufacture of most grades of paper from fibers of whatever source, it is customary to suspend previously beaten fibers, or what is generally known as pulp, in an aqueous medium for delivery to a sheet forming device, such as a Fourdrinier wire. This fiber containing aqueous dispersion is commonly referred to'in the art as a furnish. One troublesome problem at this stage of papermaking, i.e. at a point after all operations designed to modify the fibrous constituents by mechanical means have been completed and during the step of'sheet or web formation, is the tendency for the fibers to clump, coagulate or settle in the aqueous vehicle. This condition is generally referred to as flocculation, and greatly impedes the attainment of proper web formation. That is, flocculation causes a non-uniform distribution of fibers in the web, and the paper product produced therefrom manifests not only a mottled, uneven appearance but is also defective in such important physical properties as tear, burst and tensile strength.
In the manufacture of paper from conventionally used fibers, such as cellulose, methods are known-for reducing and even preventing the occurrence of flocculation. One of the more effective means has been to add a small quantity of deacetylated karaya gumto the fiber furnish. Normally from about 2 to percent on the weight of the fiber has been found to be a sutficient quantity for obtaining satisfactory results. However, this deflocculent of itself manifests so little dispersive or deflocculating potency with respect to acrylic-type fibers that only when used in massive amounts is it possible to avoid clumping of these fibers. In fact, it has been found that as much as 50' percent and sometimes 100 percent on the weight of the fiber is necessary to effect the defiooculation required for sheet formation. Obviously, the use of such large amounts of defiocculent is not .economically practical. Furthermore, the presence of such an excessive quantity of non-fibrous material is detrimental to product quality.
Accordingly, it is a primary object of this invention to provide a method for achieveing the maintenance of a uniform dispersion of acrylic-type fibers in water during the web formation step in papermaking.
It is a further object of this invention to provide a means wherein tolerable quantities of deacetylated karaya gum can be successfully employed to effect a satisfactory defiocculation of acrylic fibers in the aqueous dispersions which are employed in the papermaking process.
It is -a still further object of this invention to provide an improved process for producing paper from acrylic fibers of excellent uniformity and with superior prop- "erties.
small amounts of sulfuric acid are used in combination therewith. Thus, satisfactory results can be obtained with from 3 to 20 percent karaya gum when from 4 to 10 percent of sulfuric acid is also present in the fiber dispersion or furnish, all percentages being based on the weight of the fiber. Generally speaking, best results are achieved by employingfrom 4 to 10 percent deacetylated karaya gum and fromabout 5 to 8 percent sulfuric acid based on the Weight of the fiber present in the furnish. The order of addition has been found to be critical. That is, the sulfuric acid should be added to the fibercontaining furnish only after the karaya gum has first been introduced therein. Although the concentration of the sulfuric acid may vary in the solution thereof employed, generally it has been found convenient to add the sulfuric acid to the furnish in the form of a 1 N solution.
As in ordinary papermaking processes, the total concentration of solids present in the furnish may vary widely, for example, over a range of from 0.3 percent by weight or less up to 5 percent or more.
A simple flow diagram of the process is as follows:
Wet-spun acrylic fibers I Fibers fibrillated (pulp formation) Aqueous dispersion of fibrillated fibers prepared (furnish formation) Deacetylated karaya. gum added to furnish I Sulfuric acid added to furnish containing 'deacetylated karaya gum Furnish passed to paper forming device As noted, it has not been possible previously to main- ;tain' acrylic-type fibers satisfactorily dispersed in an aqueous medium during sheet formation with less than '50 percent of deacetylated karaya gum, based on the fiber weight, and often as much as 100 percent was required. However, by the introduction of minor quantities of sulfuric acid into the fiber dispersion with the gum deflocculent it is now possible to reduce the requirement of this agent by a factor of up to percent. Although the mechanism responsible for this effect is not fully understood, it is known that more than pH control is involved, since other strong acids, such as hydrochloric and nitric, have been found relatively ineffective.
As previously mentioned, the usefulness'of deacetylated karaya gum as a fiber defiocculent has been known heretofore, and its nature and composition have been fully described in both the literature and patents. See, for example, US. Patents 2,069,766 and 2,088,479. Consequently, only a brief discussion of this material will be undertaken here.
Gum karaya is a natural product obtained from the plant cochlospermum gossypium and allied botanical species. The product in its natural state is not an effective wdispersing agent, but is rendered so by either a complete or partial deacetylation, i.e. by substituting acetyl groups for hydroxyl groups. This can be accomplished in the following manner: First, take two parts by weight of the dry gum and form a jelly thereof in 98 parts of water. The gum maybe advantageously granulated for this purpose but should not be subjected to excessive grinding because it is susceptible to degeneration by mechanical attrition, and when thus broken down will not satisfactorily form the characteristic karaya jelly. On each 100 parts of this 2 percent karaya jelly, add 0.6 part of 26 Baum aqueous ammonia. The ammonia is mixed with the water and dispersed gum, preferably by mild rather than vigorous agitation. This effects a gradual change in the jelly over a period of from 2 to 3 hours at room temperature, which converts it into the deacetylated derivative. Best results are attained when freshly prepared deacetylated karaya gum is employed. That is to say, this material is most desirably used on the same day that it is prepared.
Although the present invention is primarily directed to the particular problem posed :by acrylic-type fibers when used in paper manufacture, the fibers which may be employed in the present invention are not restricted exclusively thereto. That is, other fibers may be blended with acrylics, such vas those derived from cellulose and other sources.
By the term acrylic fibers as used herein and in the claims, there is meant those fibers which are formed from polyacrylonitrile or copolymers thereof which contain at least 80 percent acrylonitrile in addition to one or more mono-olefinic monomers copolymerizable therewith. There is also included blended polymers and copolymers in which the blend contains at least 80 percent .acrylonitrile.
For example, the polymer may be a copolymer of from 80 to 98 percent acrylonitrile and from 2 to 20 percent of another monomer containing the C=C linkage and copolymerizable with acrylonitrile. Suitable monoolefinic monomers include acrylic, alpha-chloroacrylic [and methacrylic acids; the acrylates, such as methylmethacrylate, ethylmethacrylate, :butylmethacrylate, methoxymethyl methacrylate, beta-chloroethyl methacrylate, and the corresponding esters of acrylic and alpha-chloroacrylic acids; vinyl chloride, vinyl fluoride, vinyl bromide, vinylidene chloride, l-chloro-l-bromoethylene; methacrylonitrile; .acrylamide and methacrylamide; alphachloroacrylamide 'or monoalkyl substitution products thereof; methyl vinyl ketone; vinyl carboxylates, such as vinyl acetate, vinyl chloroacetate, vinyl propionate, and vinyl stearate; N-vinylimides, such as N-vinylphthalimide and N-vinylsuccinimide; methylene malonic esters; itaconic acid and itaconi-c ester; N-vinylcarbazole; vinyl furane; alkyl vinyl esters; vinyl sulfonic acid; ethylene alpha, beta-dicarboxylic acids or their anhydrides or derivatives, such as diethylfumarate, diethyl maleate, diethylcitraconate, diethylmesaconate; styrene; vinyl naphthalene, vinyl-substituted tertiary heterocyclic amines, such as the vinylpyridines and alkyl-substituted vinylpyridines, for example, Z-Vinylpyridine, 4-vinylpyridine, 5-methyl Q-vinylpridine, etc.; l-viny=limidazole and alkyl-substituted l-vinylimidazoles, such as 2-, 4-, or S-methyl-Z-vinylimidazole, and other C=C containing polymerizable materials. 0
The polymer may be a tertiary interpolymer, for example, products obtained by the interpolymerization of acrylonit-rile and two or more of any of the monomers, other than acrylonitrile, enumerated above. More specifically, and preferably, the ternary polymer comprises 'acrylonitrile, methacrylonitrile, and 2-vinylpyridine. The ternary polymers preferably contain from 80 to 97 percent of acrylonitrile, from 1 to percent of a vinylpyridine or a l-vinylimidazole, and from 1 to 18 percent of another substance; such as methacrylonitrile or vinyl chloride.
The blended polymers containing at least 80 percent acrylonitri-le may, for example, comprise a major amount of a polymer (A) containing at least 85 percent acrylonitrile and up to percent of one of the above-named mono-olefinic monomers copolymerizable therewith and a minor amount of a polymer (B) containing one of the vinyl-substituted alkyl pyridine monomers noted above and another of the above-named mono-olefinic monomers or acrylonitrile copolymerized therewith. These blended polymer compositions preferably contain from 50 to 98 percent of polymer (A), containing at least percent acrylonitrile and up to 15 percent of another monoolefinic monomer copolymerizable therewith, and from 2 to 50 percent of polymer (B), containing at least 30 percent of a vinyl-substituted alkyl pyridine monomer and up to 70 percent of another mono-olefinic monomer copolymerizable therewith, polymers (A) and (B) being so proportioned that the polymer blend contains from 2 to 15 percent of the vinyl-substituted alkyl pyridine monomer in polymerized form. Fibers made from the justadesoribed copolymer blend unexpectedly have a notably excellent propensity to fibrillate so that a superior paper can be manufactured therefrom.
The use of acrylic fibers formed from other than wetspinning procedures, such as by melt or dry spinning techniques are not considered useful for papermaking, inasmuch as filaments produced by the latter two methods have little tendency to 'fibrillate under the conditions which are employed in conventional papermaking processes. Consequently, the acrylic fibers contemplated for the purposes of the present invention, are those formed by the so called wet-spinning process wherein a water coagulable solution of polymeric material is extruded through a spinneret and the extruded solution is thereafter coagulated in a precipitating bath to form continuous filaments.
The following series of runs were made to test the effectiveness of sulfuric acid in accentuating the dispersive power of deacctylated karaya gum with respect to dispersions of acrylic fibers in water. The fibers employed in reach of the test samples were obtained by the wet spinning of a copolymer blend comprising 88 percent of one copolymer consisting of 94.6 percent acrylonitrile and 5.4 percent vinyl acetate and 12 percent of another copolymer consistin'g of 50 percent acrylonitrile and 50 percent methylvinyl pyridine. The fibers had an average length of one-quarter inch and a denier of 3 per filament.
Example 1 To a one liter beaker there was added a fiber-mix containing 005 gram of acrylic fiber in 500 ml. of water.
Example 2 To a second one liter beaker there was added 500 ml. of an aqueous slurry containing 0.05 gram of acrylic fiber and an amount of deacetylated karaya gum constituting 5 percent on the weight of the fiber.
Example 3 To another one liter beaker there was added 500 ml. of an aqueous slurry containing 0.05 gram of acrylic fiber and an amount of deacetylated karaya gum constituting 10 percent on the weight of the fiber.
Example 4 Example 5 To another one liter beaker there was added 500 ml.
of an aqueous slurry containing 0.05 gram of acrylic fiber and an amount of deacetylated karaya gum constituting 4 percent on the weight of the fiber. There was then slowly added a 1 N solution of sulfuric acid in an amount suificient to provide 6.8 percent sulfuric acid based on the weight of the fiber.
Example 6 To still another liter beaker there was added 500 ml. of an aqueous slurry containing 0.05 gram of acrylic Percent I Percent Example karaya sulfuric Result gum added acid added none flocculation. none D0.
' 9; 8 uniform dispersion.
6. 8 Do. 4. 9 Do.
From the above the test results, it is evident that only in those instances where sulfuric acid was employed 1n combination with the deacetylated karaya gum was it possible to avoid the occurrence of flocculation.
-In order to determine the extent of improvement in the formation of paper products produced in accordance with the present invention, another series of tests were run. In this test series paper handsheets were prepared and evaluated for formation quality. -In each of the following test samples, the fibers used in preparing the handsheets were obtained by the wet spinning of a copolymer blend comprising 88 percent of one copolymer consisting of 94.6 precent acrylonitrile and 5.4 percent vinyl acetate and 12 percent of another copolymer consisting of 50 percent acrylonitrile and 50 percent of methylvinyl pyridine. The fibers employed had been fibrillated by a 40- minute beating cycle in a conventional laboratory beater.
Example 7 A paper furnish was prepared by dispersing 2.5 grams of fibrillated fibers of the above described type in sufficient water to give a consistency of about 0.03 percent. This furnish was then added to the sheet mold of a noble and wood hand sheet machine. The dispersion was dewatered on a 100 mesh wire screen, and the resulting handsheets were couched from the wires onto standard blotting papers. The handsheets were then pressed on a roller type press, and finally dried between blotters on a steam heated drying drum.
Example 8 To the sheet mold of a paper handsheet machine partially filled with water, there was first introduced a 0.5 stock solution of freshly prepared deacetylated karaya gum. Thereafter, 2.5 grams of fibrillated acrylic fibers were added. The resulting paper furnish had a karaya gum content of percent on the weight of the fiber and a consistency of about 0.03 percent. Water was removed from the fiber dispersion by means of a 100 mesh wire screen. The resulting handsheets were then passed to standard blotting paper after which they were pressed and finally dried.
Example9 To the sheet mold of a paper handsheet machine, having been partially filled with water, there was first introduced a 0.5 stock solution of freshly prepared deacetylated karaya gum. Thereafter, 2.5 grams of fibrillated acrylic fiber were added to the mold giving a paper furnish having a consistency of about 0.03 percent with a karaya gum content of about percent on the Weight of the fiber. Water was removed from the dispersion by means of a wire screen. The resulting handsheets were then passed to standard blotting paper after which they were pressed and finally dried.
Example 10 To the sheet mold of a paper handsheet machine, having been previously partially filled with water, there was first introduced a 0.5 stock solution of freshly prepared deacetylated karaya gum. Thereafter, 2.5 grams of fibrillated acrylic fiber were added to the mold, and finally there was slowly added 3.5 ml. of a l N solution of sulfuric acid. The furnish thus prepared had a consistency of about 0.03 percent, and contained 4 percent karaya gum together with 6.8 percent sulfuric acid based on the weight of the fiber present.
Following removal of water from the furnish by means of a wire screen, the resulting handsheets were passed to standard blotting paper after which they were pressed and finally dried.
Example 1] To the sheet mold of a paper handsheet machine, having been previously partially filled with water, there was first introduced a 0.5 stock solution of freshly prepared deacetylated karaya gum. Thereafter, 2.5 grams of fibrillated acrylic fiber were added to the mold, and finally there was slowly added 3.0 ml. of a l N solution of sulfuric acid. The furnish thus prepared had a consistency of about 0.03 percent, and contained 5 percent karaya gum together with 5.8 percent sulfuric acid based on the Weight of the fiber.
Following removal of water from the furnish by utilizing a standard wire screen, the resulting handsheets were passed to standard blotting paper after which they were pressed and finally dried.
Uniformity of sheet formation was objectively measwed in each of the above examples by employing an instrument known as the 'Ihwing-A-lbert formation tester. This device utilizes a beam of light and a photo-electric cell for measuring the quality of formation. Thus, the sample to be measured is moved at high velocity between :a steady light sounce and the photo tube. The variation in opacity of the paper, which may be due to variations in either thickness or structure, cause a fluctuation in the photo-electric cell current. The fluctuations are amplified by means of an amplifier of suitable frequency characteristics, until they are of sufficient magnitude to operate a meter. The average steady photocell current is indicated on a second meter. The ratio of the readings of the two meters gives the formation value or number. The higher values or numbers are indicative of the greater uniformity in formation. The following table shows the results of the tests carried out on the above-described test samples. In the table, the use of the term percent added refers to the weight of the designated material added to the papermaking furnish based on the weight of the fiber present.
Karaya Sulfuric Formation Example gurn, peracid, pervalue cent added cent added 7 none none 16 15 none 32 20 none 35 4 6.8 44 5 5. 8 52 From the above table, it is clearly evident that substantial improvement in paper formation is realized when small quantities of sulfuric acid are employed in combination with the deacetylated karaya gum as compared with the sole use of this deflocculent.
It should be understood that although the foregoing examples describe in detail the essential features of the invention, they are intended to be illustrative only and not limitative. Thus, for example, although the invention has been illustrated in connection with the production of hand formed sheets, it is likewise applicable to the continuous production of paper sheets of indefinite lengths. That is, the fibers may be beaten in a continuous manner and then continually sheeted out on a Fourdrinier wire, rotary machine or an Oliver forming machine.
-In summary, the method of this invention provides a means for maintaining acrylic fibers uniformly dispersed in an aqueous medium by employing small amounts of sulfuric acid in combination with deacetylated karaya gum to attain excellent defiocculation. The dispersing power of the karaya gum is so greatly enhanced by the presence of small amounts of sulfuric acid that acrylic fibers can be maintained in the uniform dispersion required for paper formation with from 3 to 20 percent of this dispersing agent based on the weight of the fiber present. Heretofore, this could be accomplished only by the use of prohibitive amounts of karaya gum, i. e. from 50 to 100 percent on the weight of the fiber.
Various modifications and changes may be made in the above described process and materials that come within the scope of the invention as defined in the appended claims.
We claim:
1. In a process for making paper from an aqueous suspension of wet-spun acrylic fiblers, the step which comprises first adding, to said suspension after all operations designed to modify the fibrous constituents by mechanical means are completed and prior to the formation of the paper web, from 3, to 20 percent of deacetylated karaya gum and thereafter slowly adding as a further component from 4 to percent of sulfuric acid, all percentages being based on the weight of the fibers present in said aqueous suspension, and finally passing said aqueous suspension to a paper web forming device.
2. The process of claim 1, wherein said acrylic fibers have been obtained by the wet-spinning of a polymer blend comprising from 50 to 98 percent of one copolymer consisting of at least 85 percent acrylonitrile and up to percent of another mono-olefinic monomer copolymerizable therewith and from 2 to 50 percent of another copolymer consisting of at least percent of a vinyl-substituted alkyl pyridine and up to 70 percent of another monoolefinic monomer copolymerizable therewith.
3. The process of claim 1, wherein said acrylic fibers have been obtained by the wet-spinning of a polymer blend comprising 88 percent of one copolymer consisting of 94.6 percent 'acrylonitrile and 5.4 percent vinyl acetate and 12 percent of another copolymer consisting of percent acrylonitrile and 50 percent methylvinyl pyridine.
4. In a process for making paper from an aqueous suspension of wet-spun acrylic fibers, the step which comprises first adding to said suspension after all operations designed to modify the fibrous constituents by mechanical means are completed and prior to the [formation of the paper web, from 4 to 10 percent of deacetylated karaya gum and thereafter slowly adding as a further component from 5 to 8 percent of sulfuric acid, all percentages being based on the weight of the fibers present in said aqueous suspension,:and finally passing said aqueous suspension to a paper web forming device.
5. A stage product in the manufacture of paper from an aqueous suspension of wet-spun acrylic fibers, comprising the product obtained by first adding to said suspension after all operations designed to modify the fibrous constituents by mechanical means are completed and prior to the formation of the web, from -3 to 20 percent of deacetylated karaya gum and thereafter slowly adding as a further component from 4 to 10 percent of sulfuric acid, all percentages being based on the weight of the fibers present in said aqueous suspension.
References Cited in the fileof this patent UNITED STATES PATENTS 2,069,766 LeCompte Feb. 9, 1937 2,810,646 Wooding et a1 Oct. 22, 1957 2,930,106 Wrotnowski Mar. 29, 1960 3,016,936 Iyengar Dec. 19, 1961
Claims (1)
1. IN A PROCESS FOR MAKING PAPER FROM AN AQUEOUS SUSPENSION OF WET-SPUN ACRYLIC FIBERS, THE STEP WHICH COMPRISES FIRST ADDING, TO SAID SUSPENSION AFTER ALL OPERATIONS DESIGNED TO MODIFY THE FIBROUS CONSTITUENTS BY MECHANICAL MEANS ARE COMPLETED AND PRIOR TO THE FORMATION OF THE PAPER WEB, FROM 3 TO 20 PERCENT OF DEACETYLATED KARAYA GUM AND THEREAFTER SLOWLY ADDING AS A FURTHER COMPONENT FROM 4 TO 10 PERCENT OF SULFURIC ACID, ALL PERCENTAGES BEING BASED ON THE WEIGHT OF THE FIBERS PERCENT IN SAID AQUEOUS SUSPENSION, AND FINALLY PASSING SAID AQUEOUS SUSPENSION TO A PAPER WEB FORMING DEVICE.
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US78868A US3098786A (en) | 1960-12-28 | 1960-12-28 | Paper making process |
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US78868A US3098786A (en) | 1960-12-28 | 1960-12-28 | Paper making process |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3168802A (en) * | 1962-11-27 | 1965-02-09 | American Cyanamid Co | Synthetic paper yarn |
US3264170A (en) * | 1963-02-01 | 1966-08-02 | American Cyanamid Co | Polyacrylonitrile paper and methods for the manufacture thereof |
US3328205A (en) * | 1962-12-26 | 1967-06-27 | American Cyanamid Co | Fuel cell containing a metallized paper electrode |
US3384535A (en) * | 1961-08-29 | 1968-05-21 | Schweizerische Viscose | Process for fibrillating polyamide-containing fibers with an acid swelling agent |
US3503495A (en) * | 1968-11-29 | 1970-03-31 | Minnesota Mining & Mfg | Masking tape |
DE2715306A1 (en) * | 1976-04-06 | 1977-10-27 | Dexter Corp | PAPER MAKING PROCESS |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2069766A (en) * | 1933-11-09 | 1937-02-09 | John A Manning Paper Company I | Paper manufacture |
US2810646A (en) * | 1953-09-17 | 1957-10-22 | American Cyanamid Co | Water-laid webs comprising water-fibrillated, wet-spun filaments of an acrylonitrile polymer and method of producing them |
US2930106A (en) * | 1957-03-14 | 1960-03-29 | American Felt Co | Gaskets |
US3013936A (en) * | 1958-01-07 | 1961-12-19 | Du Pont | Synthetic fiber papers |
-
1960
- 1960-12-28 US US78868A patent/US3098786A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2069766A (en) * | 1933-11-09 | 1937-02-09 | John A Manning Paper Company I | Paper manufacture |
US2810646A (en) * | 1953-09-17 | 1957-10-22 | American Cyanamid Co | Water-laid webs comprising water-fibrillated, wet-spun filaments of an acrylonitrile polymer and method of producing them |
US2930106A (en) * | 1957-03-14 | 1960-03-29 | American Felt Co | Gaskets |
US3013936A (en) * | 1958-01-07 | 1961-12-19 | Du Pont | Synthetic fiber papers |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3384535A (en) * | 1961-08-29 | 1968-05-21 | Schweizerische Viscose | Process for fibrillating polyamide-containing fibers with an acid swelling agent |
US3168802A (en) * | 1962-11-27 | 1965-02-09 | American Cyanamid Co | Synthetic paper yarn |
US3328205A (en) * | 1962-12-26 | 1967-06-27 | American Cyanamid Co | Fuel cell containing a metallized paper electrode |
US3264170A (en) * | 1963-02-01 | 1966-08-02 | American Cyanamid Co | Polyacrylonitrile paper and methods for the manufacture thereof |
US3503495A (en) * | 1968-11-29 | 1970-03-31 | Minnesota Mining & Mfg | Masking tape |
DE2715306A1 (en) * | 1976-04-06 | 1977-10-27 | Dexter Corp | PAPER MAKING PROCESS |
US4081319A (en) * | 1976-04-06 | 1978-03-28 | The Dexter Corporation | Continuous papermaking process |
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