US3785921A - Paper reinforcing composition containing starch and a starch-acrylamide graft polymer - Google Patents
Paper reinforcing composition containing starch and a starch-acrylamide graft polymer Download PDFInfo
- Publication number
- US3785921A US3785921A US00210595A US3785921DA US3785921A US 3785921 A US3785921 A US 3785921A US 00210595 A US00210595 A US 00210595A US 3785921D A US3785921D A US 3785921DA US 3785921 A US3785921 A US 3785921A
- Authority
- US
- United States
- Prior art keywords
- acrylamide
- water
- polymer
- paper
- starch
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title abstract description 53
- 229920000578 graft copolymer Polymers 0.000 title abstract description 36
- 229920002472 Starch Polymers 0.000 title description 27
- 235000019698 starch Nutrition 0.000 title description 26
- 239000008107 starch Substances 0.000 title description 21
- 230000003014 reinforcing effect Effects 0.000 title description 19
- 239000012744 reinforcing agent Substances 0.000 abstract description 51
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract description 45
- 150000004676 glycans Chemical class 0.000 abstract description 41
- 229920001282 polysaccharide Polymers 0.000 abstract description 41
- 239000005017 polysaccharide Substances 0.000 abstract description 41
- 239000000178 monomer Substances 0.000 abstract description 39
- 229920000642 polymer Polymers 0.000 abstract description 37
- 229920001577 copolymer Polymers 0.000 abstract description 29
- 239000002253 acid Substances 0.000 abstract description 8
- 229920005604 random copolymer Polymers 0.000 abstract description 6
- 230000000379 polymerizing effect Effects 0.000 abstract description 4
- 239000000123 paper Substances 0.000 description 63
- 239000007864 aqueous solution Substances 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 238000000034 method Methods 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 14
- 238000006116 polymerization reaction Methods 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 12
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 11
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 10
- 235000013808 oxidized starch Nutrition 0.000 description 10
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 9
- 229920006322 acrylamide copolymer Polymers 0.000 description 8
- 239000012456 homogeneous solution Substances 0.000 description 8
- 239000001254 oxidized starch Substances 0.000 description 8
- -1 aluminum ion Chemical class 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 229920002554 vinyl polymer Polymers 0.000 description 7
- XMPZTFVPEKAKFH-UHFFFAOYSA-P ceric ammonium nitrate Chemical compound [NH4+].[NH4+].[Ce+4].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O XMPZTFVPEKAKFH-UHFFFAOYSA-P 0.000 description 6
- 239000000306 component Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 6
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 5
- 229920000881 Modified starch Polymers 0.000 description 5
- 239000004368 Modified starch Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 5
- 235000019426 modified starch Nutrition 0.000 description 5
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 5
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 4
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 4
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 description 3
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 3
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000010559 graft polymerization reaction Methods 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 229920001592 potato starch Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 102000001690 Factor VIII Human genes 0.000 description 1
- 108010054218 Factor VIII Proteins 0.000 description 1
- 244000017020 Ipomoea batatas Species 0.000 description 1
- 235000002678 Ipomoea batatas Nutrition 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 229940100445 wheat starch Drugs 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
- 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
- D21H17/28—Starch
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/02—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to polysaccharides
Definitions
- the DISCLOSURE Paper reinforcing agent composed mainly of a polymer composition which includes a graft polymer, a watersoluble polysaccharide, and, if necessary, an acrylamide typerandom copolymer.
- the graft polymer is that having the water-soluble polysaccharide as its backbone polymer and a copolymer derived from a monomer mixture of acrylamide and an unsaturated carboxylic acid, as its branch polymer; said random copolymer is that which is derived from the aforesaid monomer mixture.
- the Water-soluble 'polysaccharide content is -22% by Weight based on the composition.
- the paper reinforcing agent is obtained by polymerizing the aforesaid monomer mixture in the presence of the water-soluble polysaccharide, or by further adding thereto a suitable amount of the Water-soluble polysaccharide and/or the acrylamide type random copolymer.
- the reinforcing agent exhibits high paper-reinforcing property even in a small quantity and is markedly cheaper than any of the known acrylamide type paper reinforcing agents.
- This invention relates to a paper reinforcing agent having a novel composition.
- starches As the paper reinforcing agent, there have predominantly been used starches and water-soluble polysaccharides obtained by subjecting starches to such treatment as oxidation or 'etherific'ation. These starches are inexpensive. Since they are natural products, however, they have a defect that they are susceptible to weather conditions and their prices are not stable. Further, their paper-reinforcing effects are insuflicient.
- acrylamide type paper reinforcing agents have entered the limelight as dry paper reinforcing agents.
- homopolymer and copolymers of acrylamide are used as such dry paper reinforcing agents.
- the homopolymer of acrylamide is nonionic and does not easily form anionic bond with pulp. Therefore, it is difficult for the horn opolymer to provide stable adhesion to the pulp and, as a consequence, it has insufficient paper ice reinforcing capacity.
- the copolymers of acrylamide are divided into two typesanionic type and cationic type.
- the anionic copolymers include the copolymers of acrylamide with unsaturated compounds having such acid radicals as carboxyl and sulfonyl groups in their molecular units.
- the anionic copolymer exhibits strong aflinity to the pulp in the presence of such polyvalent cation as aluminum ion, with the result that the greater part of the copolymer adheres fast to the pulp. Thus, it shows excellent paper reinforcing effect even if it is used in a small amount.
- the acrylamide type paper reinforcing agents are highly effective as mentioned above, but quite expensive.
- a method is suggested in which acrylamide is copolymerized with an inexpensive nonionic monomer such as, for example, acrylonitrile, styrene or methyl methacrylate, in order to reduce the price of the anionic acrylamide type paper reinforcing agent.
- Paper reinforcing capacity is inevitably degraded as an amount of the nonionic monomer is increased.
- this method has not fully attained the goal of greatly lowering the price of paper reinforcing agent so as to permit ample use of the agent for obtaining a fixed level of paper reinforcing effect.
- Japanese patent publication No. 17,051/1963 teaches that a product obtained by polymerizing 10-300 parts of acrylamide and an unsaturated carboxylic acid in the presence of parts of a water-soluble polysaccharide is used as an additive to a heater of a paper mill.
- the product mentioned here contains as much as 25 to 91% by weight of polysaccharide, and its paper reinforcing capacity is a little more than that of a mixture of a polysaccharide and an acrylamide copolymer. Such an improvement obtained, however, is not large enough.
- a paper reinforcing agent which has, as its main ingredient, a polymer composition comprising (A) a water-soluble polysaccharide and (B) a graft polymer.
- the graft polymer (B) has (A) as the backbone polymer and a copolymer (C) as the branch polymer, said copolymer (C) being derived from a monomer mixture (D) of acrylamide and an unsaturated carboxylic acid.
- Proportion of (A) including that contained in the backbone polymer ranges from 5 to 22% by Weight, based on the entire composition.
- the present paper reinforcing agent may further be incorporated with an acrylamide type random copolymer (C') derivable from the monomer mixture (D).
- the Water-soluble polysaccharides (A) include various carbohydrates such as, for example, Indian corn starch, wheat starch, potato starch, and sweet potato starch, and derivatives thereof.
- the derivatives include oxidized starches, solubilized tarches, etherified starches, etc.
- the monomer mixture (D) is composed of 55-98% by weight of acrylamide and 2-20% by Weight of at least one unsaturated carboxylic acid of acrylic acid, methacrylic acid, maleic anhydride, itaconic acid and/or crotonic acid. Besides, up to 25% by weight of one or more vinyl monomers (E) of methacrylamide, acrylonitrile, methacrylonitrile, alkyl acrylates and/or alkyl methacrylate may be contained.
- the alkyl esters of acrylic acid or methacrylic acid include methyl, ethyl, npropyl, isopropyl, n-butyl, isobutyl, secondary butyl, tertiary butyl, hydroxyethyl and hydroxypropyl esters.
- Polymer (C) is copolymer of the monomer mixture (D), i.e. carboxylic acid-acrylamide or carboxylic acidacrylamide-vinyl compound (E).
- the polymer (C) constitutes branch polymer of the graft polymer (B), and has molecular weight of 2000 or more.
- Polymer (C) is polymer of the monomer mixture (D) in the absence of polysaccharide (A). It has molecular weight of 2000 or more. Polymer (C) is sometime the same as Polymer (C).
- Reinforcing capacity is improved conspicuously when the proportion of the water-soluble polysaccharide (A) exceeds 5% by Weight and it is maximized when the proportion falls in the neighborhood of -15% by weight.
- the capacity begins to decline gradually when the proportion exceeds by weight. If the proportion increases over 22%, the capacity become substantially equal to the capacity attained by using the acrylamide copolymer alone. If the proportion further increases, the capacity abruptly approaches the level of capacity calculated on the assumption that the acrylamide copolymer and the water-soluble polysaccharide act independently. Thus, the advantages derived from the graft polymer is lost practically completely.
- the amount of the un aturated carboxylic acid present in the monomer mixture (D) is required to fall in the range of from 2 to This is an important requirement for the paper reinforcing agent to manifest its excellent effect as contemplated.
- the paper reinforcing agent has a lower degree of reinforcing capacity than when the acrylamide copolymer is used alone.
- Random terpolymer such as, for example, acrylamide, acrylonitrile and unsaturated carboxylic acid
- random binary copolymer such as, for example, acrylamide and unsaturated carboxylic acid
- the paper reinforcing agent of this invention can be obtained by either of the following methods:
- the monomer mixture (D) is polymerized in the presence of such an amount of the water-soluble polysaccharide (A) as to give a proportion of 522% by weight in the total composition.
- the monomer mixture (D) is polymerized in the presence of the water-soluble polysaccharide (A) and then the water-soluble polysaccharide (A) and/or the acrylamide type copolymer (C) is added to the resultant polymerization product in such an amount that (A) in the total composition may be in the range of 522% by weight.
- the method of (ii) is preferable, because the ratio of graft polymer (B) in the composition, the average molecular weight and an amount of the acrylamide type copolymer (C), and the proportion of unaltered water soluble polysaccharide can freely be varied.
- the proportion of the graft polymer (B) in the composition can be controlled at a suitable value by adding the acrylamide copolymer (C) to the graft polymer (B). It is no matter how much grafting degree of the graft polymer (B) may be.
- the medium to be used for this purpose may be either a solvent or non-solvent for the polymer being produced.
- water is used as the medium.
- the water-soluble polysaccharide may preferably be converted in advance to a homogeneous solution by being heated to a temperature exceeding the gelatinizing point and then put to use in the form of solution.
- the catalysts which are suitable for the polymerization in the medium of water include ammonium persulfate, potassium persulfate, hydrogen peroxide, etc. Redox catalysts made of such peroxides and such reducing substances as amines may also be used.
- water-soluble ceric salts, such as ceric ammonium nitrate, are also usable. These ceric salts are capable of causing water-soluble polysaccharides to form radicals. If a ceric.
- component (B) it is desirable to control the contents of component (B) by adding thereto a suitable amount of the acrylamide type copolymer (C) obtained by polymerizing the monomer mixture (D) and/or the water-soluble polysaccharide capacity which is obtained by using the water-soluble polysaccharide, the acrylamide type graft polymer, or the acrylamide type random copolymer alone.
- a suitable amount of the acrylamide type copolymer (C) obtained by polymerizing the monomer mixture (D) and/or the water-soluble polysaccharide capacity which is obtained by using the water-soluble polysaccharide, the acrylamide type graft polymer, or the acrylamide type random copolymer alone.
- Each example describes a method for manufacturing the paper reinforcing agent of this invention.
- the properties of the agents prepared in these examples are collectively shown in the table given at the end of the text. Parts and percent all are referred to by weight.
- EXAMPLE 1 The aqueous solution of a polymer containing soluble starch by 10% based on the polymer was obtained by following the procedure of Example 1, except there were used 10 parts of soluble starch and 90 parts of a monomer mixture incorporating acrylic acid in place .of the' methacrylic acid.
- EXAMPLE 3 The aqueous solution of a polymer containing soluble starch by 15 based on the polymer was obtained by following the procedure of Example 1, except there were used 15 parts of soluble starch and parts of monomer mixture. l
- EXAMPLE 4 The aqueous solution of a polymer containing soluble starch by 22% based on the polymer was obtained by following the procedure of Example 1, except there were used 22 parts of soluble starch and 78 parts of monomer mixture.
- the paper reinforcing agent of the present invention has outstanding reinforcing capacity as comparedwith the EXAMPLE 5
- 900 parts of water were dissolved 15 parts of soluble starch and 85 parts of a monomer mixture consisting of 95% of acrylamide and 5% of methacrylic acid.
- the solution was adjusted to pH 2.5 with nitric acid and displaced thoroughly with N
- the solution was subjected to polymerization at 50 C. for six hours to afford the aqueous solution of a graft polymer.
- EXAMPLE 6 In 450 parts of water were dissolved 45 parts of acrylamide and 5 parts of acrylic acid. The solution was adjusted to pH 7.0 and, in the presence of 1.0 part of potassium persulfate added thereto, subjected to polymerization at 60 C. for two hours to aiford the copolymer of acrylamide. The copolymer was mixed with the aqueous solution of graft polymer obtained by the procedure of Example 5, to afford a homogeneous solution.
- EXAMPLE 7 Ten parts of oxidized starch was suspended in 40 parts of water and then dissolved by heating. The resultant aqueous solution was combined with the aqueous solution of graft polymer obtained by following the procedure of Example 1, to form a homogeneous solution.
- EXAMPLE 8 Five (5) parts of oxidized starch was suspended in 45 parts of water and dissolved by heating to afford the aqueous solution of oxidized starch. Separately, 45 parts of acrylamide and 5 parts of acrylic acid were dissolved in 450 parts of water. The solution was adjusted to pH 7.0 and, in the presence of 0.5 part of ammonium persulfate added thereto, subjected to polymerization at 60 C. for four hours, to afford the aqueous solution of acrylamide copolymer. The two aqueous solutions thus prepared were mixed with the aqueous solution of graft polymer obtained by following the procedure of Example 2, to obtain a homogeneous solution. 7
- EXAMPLE 9 Ten (10) parts of oxidized starch was dissolved by heating in 900 parts of water. In the resultant solution were further dissolved 2 parts of acrylamide, 10 parts of acrylonitrile, and 8 parts of acrylic acid. The final solution was adjusted to pH 2.5 with nitric acid. This was displaced thoroughly with nitrogen and, in the presence of 1.5 parts of ceric ammonium nitrate, subjected to polymerization at 50 C. for eight hours, to afford the aqueous solution of graft polymer (A). Separately, 5 parts of soluble starch was dissolved by heating in 45 parts of water. This solution was combined with the aqueous solution of graft polymer (A), to produce a homogeneous solution.
- EXAMPLE 10 In 450 parts of water were dissolved 35 parts of acrylamide, 10 parts of methyl acrylate, and 5 parts of methacrylic acid. The solution was adjusted to pH 7.0 and, in the presence of 0.5 part of potassium persulfate added thereto, subjected to polymerization at 60 C. for four hours, to produce the aqueous solution of copolymer having acrylamide as the main component. The aqueous solution was combined with the aqueous solution of graft polymer synthesized by following the procedure of Example 5, to afford a homogeneous solution.
- EXAMPLE 11 In 270 parts of water were dissolved 25 parts of acrylamide, 3 parts of methacrylic'acid, and 2 parts of acrylonitrile. The solution was adjusted to pH 7.0 and, in the presence of 0.5 part of ammonium persulfate added thereto, subjected to polymerization at 60 C. for four hours,
- COMPARATIVE EXAMPLE 1 In 900 parts of water were dissolved 90 parts of acrylamide and 10 parts of acrylic acid. The solution was adjusted to pH 7.0 and, in the presence of 2 parts of potassium persulfate added thereto, subjected to polymerization at 60 C. for two hours, to produce the copolymer of acrylamide.
- COMPARATIVE EXAMPLE 2 The solution obtained by dissolving 10 parts of oxidized starch under heating in 90 parts of water was combined with the aqueous solution of acrylamide copolymer obtained by following the procedure of Comparative Example 1, to afford a homogeneous solution.
- COMPARATIVE EXAMPLE 3 The aqueous solution of graft polymer containing soluble starch by 25% based on the polymer was obtained by following the procedure of Example 1, except there were used 25 parts of soluble starch and 75 parts of monomer mixture.
- COMPARATIVE EXAMPLE 4 In 9 00 parts of water were dissolved 15 parts of oxidized starch and parts of acrylamide. In the presence of 1.0 part of potassium persulfate added thereto, the solution was subjected to polymerization at 60 C. for three hours to afford the aqueous solution of graft polymer.
- COMPARATIVE EXAMPLE 5 In 900 parts of water were dissolved 15 parts of oxidized starch and 85 parts of a monomer mixture consisting of 75% of acrylamide and 25% of methacrylic acid. The solution was adjusted to pH 7.0 and, in the presence of 1.0 part of ammonium persnlfate added thereto, subjected to polymerization at 60 C. for four hours, to afford the aqueous solution of graft polymer.
- Papers using the polymer solutions of Examples 1-11 and Comparative Examples 1-5 as paper reinforcing agents were fabricated by the Tappi standard sheet machine and then tested for strength.
- the papers were made of pulp LBKP (bleached kraft pulp of broad-leaf trees) having Canadian Standard freeness 390 ml.
- the basis weight was 60-62 g./m.
- As the sizing agent rosin maleate was used in an amount corresponding to 1.5% based on the pulp.
- Aluminum sulfate was used in an amount corresponding to 2.0% based on the pulp.
- the amount of paper reinforcing agent used was 0.5% based on the pulp.
- Burst factor was measured with Miillen burst strength tester and breaking length with Schopper tensile machine respectively at 20 C. and 65% RH.
- G graft polymerization product
- B blended composition
- GB graft polymerized and blended product.
- a paper reinforcing agent having, as its main component, a composition consisting essentially of (A) a watersoluble polysaccharide selected from the group consisting of starch and modified starch and (B) a graft polymer, said graft polymer having (A) as a backbone polymer and a copolymer (C) as a branch polymer, said copolymer (C) being the reaction product of a monomer mixture (D) consisting of 80 to 98% by weight of acrylamide and 2 to 20% by weight of at least one unsaturated carboxylic acid and derivatives thereoof selected from the group consisting of acrylic acid, methacrylic acid, maleic anhydride, itaconic acid and crotonic acid, and the proportion of (A) including that contained in the backbone polymer falling in the range of from to 22% by weight based on the entire composition.
- A a watersoluble polysaccharide selected from the group consisting of starch and modified starch
- B a graft polymer
- a paper reinforcing agent having, as its main component, a composition consisting essentially of (A) a water-soluble polysaccharide selected from the group consisting of starch and modified starch, (B) a graft copolymer and (C') a copolymer derived from a monomer mixture (D), said monomer mixture (D) being made up of 80 to 98% by weight of acrylamide and 2 to 20% by weight of at least one unsaturated carboxylic acid and derivatives thereof selected from the group consisting of acrylic acid, methacrylic acid, maleic anhydride, itaconic acid, and crotonic acid, and said graft polymer (B) having (A) as a backbone polymer and the copolymer (C') as a branch polymer, the proportion of (A) in the composition falling in the range of from 5 to 22% by weight.
- a paper reinforcing agent having as its main compo nent a composition consisting essentially of (A) a watersoluble polysaccharide selected from the group consisting of starch and modified starch and (B) a graft polymer, said graft polymer having the watersoluble polysaccharide (A) as a backbone polymer and a copolymer (C) as a branch polymer, said copolymer (C) being the reaction product of a monomer mixture consisting essentially of from 55 to 98% by weight of acrylamide, 2 to 20% by weight of an unsaturated carboxylic acid and derivatives thereof selected from the group consisting of acrylic acid, methacrylic acid, maleic anhydride, itaconic acid and crotonic acid, and up to 25% by weight of at least one vinyl monomer selected from the group consisting of methacrylamide, acrylonitrile, methacrylonitrile, alkyl acrylates and alkyl methacrylates, and the proportion of the water-soluble polysacc
- a paper reinforcing agent having as its main component a composition consisting essentially of (A) a watersoluble polysaccharide selected from the group consisting of starch and modified starch, (B) a graft copolymer and (C') a coplymer derived from a monomer mixture (D), said monomer mixture (D) consisting essentially of from 55 to 98% by weight of acrylamide, 2 to 20% by weight of an unsaturated carboxylic acid and derivatives thereof selected from the group consisting of acrylic acid, methacrylic acid, malcic anhydride, itaconic acid and crotonic aid, and up to 25% by weight of at least one vinyl monomer selected from the group consisting of methacrylamide, acrylonitrile, methacrylonitrile, alkyl acrylates, and alkyl methacrylates, and said graft polymer (B) having the watersoluble polysaccharide (A) as a backbone polymer and (C') as a branch polymer, the proportion of (
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Paper (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP45129611A JPS5247044B1 (enrdf_load_stackoverflow) | 1970-12-26 | 1970-12-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3785921A true US3785921A (en) | 1974-01-15 |
Family
ID=15013729
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00210595A Expired - Lifetime US3785921A (en) | 1970-12-26 | 1971-12-21 | Paper reinforcing composition containing starch and a starch-acrylamide graft polymer |
Country Status (4)
Country | Link |
---|---|
US (1) | US3785921A (enrdf_load_stackoverflow) |
JP (1) | JPS5247044B1 (enrdf_load_stackoverflow) |
CA (1) | CA949691A (enrdf_load_stackoverflow) |
FR (1) | FR2124662A5 (enrdf_load_stackoverflow) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4134863A (en) * | 1976-12-06 | 1979-01-16 | The United States Of America As Represented By The Secretary Of Agriculture | Highly absorbent graft copolymers of polyhydroxy polymers, acrylonitrile, and acrylic comonomers |
EP0011303A3 (en) * | 1978-11-20 | 1980-08-20 | Cpc International Inc. | Process for the manufacture of paper, paper additive composition and paper of improved surface properties |
US4278573A (en) * | 1980-04-07 | 1981-07-14 | National Starch And Chemical Corporation | Preparation of cationic starch graft copolymers from starch, N,N-methylenebisacrylamide, and polyamines |
US4323487A (en) * | 1979-10-22 | 1982-04-06 | Henkel Corporation | Absorbent starch graft polymer and method of its preparation |
US4330365A (en) * | 1980-04-07 | 1982-05-18 | National Starch And Chemical Corporation | Paper containing cationic starch graft copolymers from starch, N,N'-methylenebisacrylamide, and polyamines |
EP0130961A1 (en) * | 1983-06-02 | 1985-01-09 | Monsanto Company | Viscosity modifiers for grafted starch polymer solutions |
EP0257412A1 (de) * | 1986-08-14 | 1988-03-02 | BASF Aktiengesellschaft | Leimungsmittel für Papier auf Basis feinteiliger wässriger Dispersionen |
EP0276770A3 (en) * | 1987-01-30 | 1988-08-24 | Basf Aktiengesellschaft | Paper-sizing agent based on particulate aqueous dispersions |
EP0405917A1 (en) * | 1989-06-26 | 1991-01-02 | Sequa Chemicals Inc. | Starch polymer graft |
EP0405921A1 (en) * | 1989-06-26 | 1991-01-02 | Sequa Chemicals Inc. | Starch binder composition |
US5055541A (en) * | 1989-06-27 | 1991-10-08 | Sequa Chemicals, Inc. | Starch polymer graft composition and method of preparation |
US5294301A (en) * | 1991-05-30 | 1994-03-15 | National Starch And Chemical Investment Holding Corporation | Process for manufacture of paper |
US6787574B1 (en) | 2000-10-24 | 2004-09-07 | Georgia-Pacific Resins, Inc. | Emulsification of alkenyl succinic anhydride size |
US20050153421A1 (en) * | 2002-03-22 | 2005-07-14 | Kozo Murao | Aqueous acrylamide solution containing saccharide |
RU2733729C2 (ru) * | 2016-03-01 | 2020-10-06 | Кемира Ойй | Полимерная композиция, ее применение и поверхностная проклейка |
-
1970
- 1970-12-26 JP JP45129611A patent/JPS5247044B1/ja active Pending
-
1971
- 1971-12-16 CA CA130,244A patent/CA949691A/en not_active Expired
- 1971-12-21 US US00210595A patent/US3785921A/en not_active Expired - Lifetime
- 1971-12-24 FR FR7146606A patent/FR2124662A5/fr not_active Expired
Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4134863A (en) * | 1976-12-06 | 1979-01-16 | The United States Of America As Represented By The Secretary Of Agriculture | Highly absorbent graft copolymers of polyhydroxy polymers, acrylonitrile, and acrylic comonomers |
EP0011303A3 (en) * | 1978-11-20 | 1980-08-20 | Cpc International Inc. | Process for the manufacture of paper, paper additive composition and paper of improved surface properties |
US4323487A (en) * | 1979-10-22 | 1982-04-06 | Henkel Corporation | Absorbent starch graft polymer and method of its preparation |
US4278573A (en) * | 1980-04-07 | 1981-07-14 | National Starch And Chemical Corporation | Preparation of cationic starch graft copolymers from starch, N,N-methylenebisacrylamide, and polyamines |
US4330365A (en) * | 1980-04-07 | 1982-05-18 | National Starch And Chemical Corporation | Paper containing cationic starch graft copolymers from starch, N,N'-methylenebisacrylamide, and polyamines |
EP0130961A1 (en) * | 1983-06-02 | 1985-01-09 | Monsanto Company | Viscosity modifiers for grafted starch polymer solutions |
EP0257412A1 (de) * | 1986-08-14 | 1988-03-02 | BASF Aktiengesellschaft | Leimungsmittel für Papier auf Basis feinteiliger wässriger Dispersionen |
US4855343A (en) * | 1986-08-14 | 1989-08-08 | Basf Aktiengesellschaft | Paper size based on finely divided aqueous dispersions |
EP0276770A3 (en) * | 1987-01-30 | 1988-08-24 | Basf Aktiengesellschaft | Paper-sizing agent based on particulate aqueous dispersions |
EP0405921A1 (en) * | 1989-06-26 | 1991-01-02 | Sequa Chemicals Inc. | Starch binder composition |
EP0405917A1 (en) * | 1989-06-26 | 1991-01-02 | Sequa Chemicals Inc. | Starch polymer graft |
US5026746A (en) * | 1989-06-26 | 1991-06-25 | Sequa Chemicals, Inc. | Starch based binder composition for non-woven fibers or fabrics |
US5055541A (en) * | 1989-06-27 | 1991-10-08 | Sequa Chemicals, Inc. | Starch polymer graft composition and method of preparation |
US5294301A (en) * | 1991-05-30 | 1994-03-15 | National Starch And Chemical Investment Holding Corporation | Process for manufacture of paper |
US6787574B1 (en) | 2000-10-24 | 2004-09-07 | Georgia-Pacific Resins, Inc. | Emulsification of alkenyl succinic anhydride size |
US20050153421A1 (en) * | 2002-03-22 | 2005-07-14 | Kozo Murao | Aqueous acrylamide solution containing saccharide |
US7129217B2 (en) * | 2002-03-22 | 2006-10-31 | Dia-Nitrix Co., Ltd. | Aqueous acrylamide solution containing saccharide |
AU2003221403B2 (en) * | 2002-03-22 | 2008-02-21 | Mitsubishi Chemical Corporation | Aqueous acrylamide solution containing saccharide |
CN100462372C (zh) * | 2002-03-22 | 2009-02-18 | 大野绿水株式会社 | 含糖类的丙烯酰胺水溶液 |
RU2733729C2 (ru) * | 2016-03-01 | 2020-10-06 | Кемира Ойй | Полимерная композиция, ее применение и поверхностная проклейка |
US11447618B2 (en) | 2016-03-01 | 2022-09-20 | Kemira Oyj | Polymer composition, its use and a surface size |
Also Published As
Publication number | Publication date |
---|---|
JPS5247044B1 (enrdf_load_stackoverflow) | 1977-11-30 |
FR2124662A5 (enrdf_load_stackoverflow) | 1972-09-22 |
CA949691A (en) | 1974-06-18 |
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