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
  • D21H17/33—Synthetic macromolecular compounds
  • D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds

Definitions

• paper composed of a waterlaid web of cellulosic papermaking fibers bonded together by a small adsorbed amount of a normally water-soluble linear carbon chain polymer con- .taining carbamyl and hydroxyamidino side groups (as more particularly hereinafter described) possesses substantially improved dry strength and yet possesses low wet strength.
• the dry tensile strength of paper of the present invention is improved by about 50%75% as a result of the strengthening action of the polymer, and dry burst values are improved by upward of 75%85%.
• the paper '(at ordinary book paper weight) possesses a wet tensile strength of less than about 3 lbs./in., which means that it can be repulped in ordinary papermill equipment.
• the polyacrylamidoxime polymer of the present invention is soluble in water yet is substantively adsorbed therefrom by cellulose fibers. Accordingly, paper of the present invention is manufactured by forming an aqueous suspension of papermaking cellulosic fibers, adding thereto a small amount of an aqueous solution of polyacrylamidoxime polymer, sheeting the fibers to form a cellulosic web, and heating the web until dry.
• the polymers of the present invention are non-thermosetting and thus do not require heat for development of their strengthening properties. However, they are thermostable and thus the wet webs may be dried without harm on steam-heated rolls in the customary temperature range of 190 F. to 250 F.
• the polymer is well adsorbed by fibers which have been rosin sized, and the beneficial effect of the polymer in increasing the dry strength is not significantly v diminished by the presence of such sizing on the fibers.
• vention is ampholytic, and thus may be applied as an anionic or cationic material. It is insensitive to pH and affords substantially the same results at pH 6.5 as at pH 3.5. The evidence is that somewhat better dry strength is developed when the pH of the suspension during addition of the polymer is between 4.5 and 6.5, and this range accordingly is preferred.
• Best dry strength values are usually obtained when the fibrous suspension during addition of the polymer contains alum. Since the polymer is self-substantive the alum does not appear to act as mordant or precipitant. Evidently the paper produced from suspensions containing alum carries the polymer in the form of an alum complex. About of dissolved alum in the suspension (based on the dry weight of cellulose fibers) is sufiicient to cause a substantial increase in the dry strength imparted by the resin, and more than about 2% appears to be unnecessary for the purpose. An intermediate amount in the range of /;%-1%% is accordingly preferred, it being understood that much larger amounts may be present without harm. With or without alum, adsorption of the polymer by the fibers is substantially complete.
• the polymer employed in the present invention consists predominantly of hydroxyamidinoethylene and carbamylethylene linkages,"the theoretical formulaelof which are NH CHzCH(CNHOH)-- and 0 CH CH(CNHa)'
• the former linkage may exist in the tautomeric form and moreover two adjacent hydroxyamidino substituents may react or coordinate to form ,a linkage of the type to.
• HON g NOH Paper containing polymers having such linkages is within the scope of the invention.
• polymers containing additional groups which act as diluents, or spacers, or which act in known manner for other purposes may carry in minor, proportion alkyl or aryl, alkoxy, hydroxyl, carboxyl, ester, amine, carboxy, quaternary ammonium, and nitrile groups as supplemental substituents. Up to 50 mol percent of such substituents may be present, it being understood that in the case of the hydrophobic substituents the amounts thereof should be limited so that the polymer remains water-soluble to the extent of at least 5%.
• the hydroxyamidino and carbamyl groups of the polymer are active ionically and evidently serve two principal functions.
• the first is to provide electrostatic loci, capable of acting ionically by which the polymer macromolecule as a whole is attracted to and substantively adsorbed by cellulose fibers in aqueous suspension in the presence or absence of dissolved polyvalent metal salts.
• the second function is to provide dry 3 strength.
• the hydroxyamidino grouping is effective electrostatically in very small amounts and as little as 1% based on the remaining substituents present has been sufiicient to render the macromolecule cationically active and self-substantive to cellulose.
• Considerable improvement in the dry strength is obtained by use of polymers containing a larger proportion of these groupings, particularly when the polymer contains hydroxyamidinoethylene and carbamylethylene linkages in ratio between about 1:10 and 3:10.
• Increasing the proportion of hydroxyamidino groups in the macromolecule results in further improvement in dry strength. This improvement, however, becomes progressively less as the proportion rises above this ratio range and accordingly the range stated is regarded as the practical maximum.
• the carbamylethylene linkages which constitute the other major functional grouping in the polymer are ionically inert, but powerfully coordinate or react with the cellulose to provide dry strength. Apparently for the latter purpose they are somewhat more effective than the hydroxyamidinoethylene linkages, and accordingly, the number of carbamylethylene linkages should be at least of the number of hydroxyamidinoethylene linkages.
• the polymers employed in the present invention may be prepared in any convenient manner. In practice they are most conveniently prepared by copolymerizing a watersoluble vinyl nitrile and a water-soluble vinyl amide in major proportion with or without supplementary or di1uent vinyl material to form an essentially linear carbon chain amide-nitrile polymer.
• nitrile groups are then reacted with hydroxylamine to form hydroxyamidino groups in the proportion specified. It is preferred to form the polymer by copolymerizing acrylonitrile (methacrylonitrile, crotononitrile, etc.) with acrylamide or similar amide having an unsubstituted -NH amide substituent in molar ratio between about 70:30 and 90:10 and then heating with hydroxylamine to convert nitrile groups to hydroxyamidino groups in proportion specified above.
• acrylonitrile methacrylonitrile, crotononitrile, etc.
• the polymer may be subjected to other reactions before or after the hydroxylamine reaction, and thus any ester groups present may be subjected to hydrolysis to form hydroxy or acid groups; any nitro groups present may be reduced to amine groups; any chloro groups may be reacted with tertiary amines to form quaternary ammonium groups.
• the vinyl polymerization leading to formation of the linear chain polymer may be performed in aqueous medium using a redox catalyst, and molecular growth to an advanced stage should be favored.
• the development of increased dry strength requires the use of polymers having a molecular weight in excess of about 100,000 (as determined by the Staudinger method based on viscosity) and considerably better results are obtained when the molecular weight is upwards of 500,000, which is the preferred lower limit.
• the polymers are too viscous for commercial use at molecular weights in excess of 5,000,000 and this therefore is the maximum of the preferred range.
• Example 1 The following illustrates the manufacture of paper of excellent dry tensile strength but low wet strength according to the present invention by use of a preferred hydroxyamidinoethylene-carbamylethylene polymer.
• the resin was prepared by dissolving 5.0 gm. of an 80%20% (molar ratio) acrylamidezacrylonitrile polymer (molecular weight 500,000) in 200 ml. of water, adding 0.655 gm. of hydroxylamine hydrochloride (equivalent to 64% of the nitrile groups present), adjusting the pH to 6.8 with dilute aqueous NaOH solution, and heating the mixture for 30 minutes at C.
• the resulting polymer was substantially composed of carbamylethylene, hydroxyamidinoethylene and cyanoethylene linkages in approximately 8:1:1 molar ratio, and was diluted to 5% solids with water and cooled.
• Dry strength paper containing the resin was made by standard laboratory procedure using 50:50 bleached sulfitezbleached hardwood kraft pulp. The pulp was diluted to 0.6% consistency, aliquots withdrawn, and the polymer solution added with and without alum as shown in the table, the alum when used being added before the polymer. After addition of the polymer the aliquots were gently stirred for 5 minutes and then sheeted on a Nash handsheet machine at 45-50 lb. basis weight (25" x 40/500 ream). The sheets were drum dried for one minute at 250 F. and tested after conditioning at 73 C. and 50% relative humidity for 24 hours.
• Example 2 The following illustrates the improved results obtained with rosin size when the size is supplied in conjunction with a linear polymer carrying hydroxyamidino groups.
• the papers were made according to the method of Example 1, wood rosin size and alum being added prior to the polymer. Results are as follows, the first three runs being controls.
• Example 3 The following illustrates the improvements in dry strength obtained by additional hydroxyamidinoethylene-carbamylethylene polymers.
• the general method of Example 1 was followed for preparation of the polymers and manufacture of the paper samples, 0.5% of polymer being added to the pulp samples in each instance.
• Polymers 1-4 were prepared by copolymerizing acrylonitrile and acrylamide and then reacting with hydroxylamine to convert nitrile groups to the proportion of hydroxyamidino groups as shown in the table.
• polymer No. 1 was prepared by copolymerizing acrylamide and acrylonitrile in 80:20 molar ratio and then reacting with hydroxylamine calculated as equivalent to 75% of the acrylonitrile.
• Polymer 5 was prepared by copolymerizing acrylamide, acrylonitrile and vinyl acetate in :40:50 molar ratio and then reacting with hydroxylamine to convert 87% 10 I claim:
• Paper of substantially improved dry strength but of low wet strength composed of a waterlaid web of cellulosic papermaking fibers bonded together by 0.1%- 5%, based on the dry weight thereof, of a normally water-soluble ampholytic linear carbon chain vinyl polymer predominantly composed of recurring hydroxyamidinoethylene and carbamylethylene linkages, the ratio between said linkages being between about 1:100 and 10:1, said polymer having a molecular weight in excess of 100,000.
• Example 4 Results are as follows. The first four runs are controls.
• Sized paper of substantially improved dry strength but of low wet strength and of improved resistance to penetration by aqueous fluids composed of a waterlaid web of rosin sized cellulosic papermaking fibers bonded together by 0.1%5%, based on the dry weight of said fibers, of a normally water-soluble ampholytic linear carbon chain vinyl polymer predominantly composed of recurring hydroxyamidinoethylene and carbamylethylene linkages, the ratio between said linkages being between about 1:100 and 10: 1, said polymer having a molecular weight in excess of 100,000 and acting synergistically with said size to render said fibers resistant to penetration by aqueous fluids.
• Process for the manufacture of paper of substantially improved dry strength but of low wet strength which comprises forming an aqueous suspension of papermaking cellulosic fibers, adding thereto between about 0.1% to 5%, based on the dry weight of the fibers, of a water-soluble ampholytic liner carbon chain vinyl polymer substantially composed of recurring hydroxyamidinoethylene and carbamylethylene linkages, the ratio between said linkages being between about 1:100 and 10:1, said polymer having a molecular weight in excess of 100,000, whereby said polymer is adsorbed on said fibers, sheeting said fibers to form a cellulosic web, and heating said web until dry at a temperature between F. and 250 F.
• sus 7 pension during addition of the polymer contains between about 0.1% and 2% of alum based on the dry weight of the fibers.

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• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Paper (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

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Cited By (3)

Citations (6)

• 0
  • BE BE575756D patent/BE575756A/xx unknown
• 1958
  • 1958-02-17 US US715488A patent/US2959514A/en not_active Expired - Lifetime
• 1959
  • 1959-02-12 GB GB4910/59A patent/GB845349A/en not_active Expired
  • 1959-02-14 FR FR786750A patent/FR1225728A/fr not_active Expired

Patent Citations (6)

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