GB1127177A - Paper of improved dry strength and process for preparing it - Google Patents

Paper of improved dry strength and process for preparing it

Info

Publication number
GB1127177A
GB1127177A GB45136/65A GB4513665A GB1127177A GB 1127177 A GB1127177 A GB 1127177A GB 45136/65 A GB45136/65 A GB 45136/65A GB 4513665 A GB4513665 A GB 4513665A GB 1127177 A GB1127177 A GB 1127177A
Authority
GB
United Kingdom
Prior art keywords
mol
epichlorohydrin
water
paper
functionality
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
Application number
GB45136/65A
Inventor
Norman Thorndike Woodberry
Walter Florus Reynolds
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB1127177A publication Critical patent/GB1127177A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/46Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/54Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
    • D21H17/56Polyamines; Polyimines; Polyester-imides

Abstract

1,127,177. Paper. AMERICAN CYANAMID CO. 25 Oct., 1965, No. 45136/65. Headings D2A and D2B. Paper of improved dry tensile strength but low wet strength is substantially composed of water-laid fibres of unbleached cellulose, bonded together by an ionically adsorbed content of a normally water-soluble, two-dimensional, non-thermosetting cationic polyamine containing at least five amino nitrogen atoms per macromolecule, and having a molecular weight between 1,000 and 10,000. The fibres may contain more than 1 % of acidic lignin material, and the polyamine may be used in amount sufficient to neutralize substantially all of this material. The polyamine may be formed by reacting substantially completely, to a point short of gelation, epichlorohydrin with a major proportion of water-soluble "bifunctional" amine and a minor proportion of water-soluble "polyfunctional" amine, the ratio of the "functionality" of the epichlorohydrin to the total "functionality" of the amines being substantially 1:1. "Bifunctional" and "polyfunctional" are defined as meaning capable of reacting twice or more than twice, respectively, with epichlorohydrin; and "functionality" as number of reactive functions present. In the Examples: (A) 1.2 mol of aqueous methylamine, 0.2 mol of ethylendiamine, and 1.6 mol of epichlorohydrin are reacted in a flask in the presence of water and of sodium hydroxide in the later stages, the solution is then neutralized with acetic acid and cooled: (B) 1 mol of methylamine, 0.2 mol of ammonia and' 1.3 mol of epichlorohydrin are reacted similarly, the final neutralization being with HC1: (C) 1.25 mol of tetraethylenpentamine is heated with 1.25 mol of adipic acid. and the product dissolved in water. 0.275 mol of epichlorohydrin is added. and after reaction the solution is acidified with HCl: (D) as C, but using methylenebisacrylamide in place of epichlorohydrin; (E) as C. but using 1.2-dichlorethane in place of epichlorohydrin; (F) one mol of tetraethylenpentamine is reacted with 1.2 mol of dichlorethane in the presence of water, and 1.2 mol of NaOH added to neutralize the acid formed. Papers are made by adding these polymers to unbleached pulp, sheeting out and drying. Fillers may also be present, e.g. ultramarine, clay, TiO., and calcium carbonate, or basic dyes. Any broke arising is readily repulped.
GB45136/65A 1964-01-30 1965-10-25 Paper of improved dry strength and process for preparing it Expired GB1127177A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US341413A US3258393A (en) 1964-01-30 1964-01-30 Dry strength paper containing unbleached cellulosic fibers and a non-thermosetting cationic polyamine

Publications (1)

Publication Number Publication Date
GB1127177A true GB1127177A (en) 1968-09-11

Family

ID=23337452

Family Applications (1)

Application Number Title Priority Date Filing Date
GB45136/65A Expired GB1127177A (en) 1964-01-30 1965-10-25 Paper of improved dry strength and process for preparing it

Country Status (5)

Country Link
US (1) US3258393A (en)
AU (1) AU6552365A (en)
FR (1) FR1455530A (en)
GB (1) GB1127177A (en)
NL (1) NL6514656A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023283710A1 (en) 2021-07-15 2023-01-19 Klabin S.A. Dispersible paper, method for producing same, packaging and use of said paper

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4102738A (en) * 1977-01-17 1978-07-25 American Cyanamid Company Use of chitosan in corrugating medium
CN112551937B (en) * 2020-12-07 2022-08-05 绵竹市铸诚混凝土有限公司 Composite additive for fair-faced concrete, fair-faced concrete and preparation method of fair-faced concrete

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2884057A (en) * 1954-02-25 1959-04-28 American Cyanamid Co Paper of improved dry strength and method of making same
US2834675A (en) * 1954-06-10 1958-05-13 American Cyanamid Co Polyalkylene-polyamine resinous composition, method of making paper using same and paper containing same
US3019156A (en) * 1957-04-29 1962-01-30 American Cyanamid Co Wet strength paper containing polyamide
US3086961A (en) * 1959-12-07 1963-04-23 American Cyanamid Co Water-soluble dibasic acid-polyalkylenepolyamine-alkylene glycol crosslinked polymer

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023283710A1 (en) 2021-07-15 2023-01-19 Klabin S.A. Dispersible paper, method for producing same, packaging and use of said paper

Also Published As

Publication number Publication date
US3258393A (en) 1966-06-28
AU6552365A (en) 1967-04-20
FR1455530A (en) 1966-04-01
NL6514656A (en) 1967-05-12

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