GB1406336A - Process for the treatment of paper pulp - Google Patents

Process for the treatment of paper pulp

Info

Publication number
GB1406336A
GB1406336A GB2504773A GB2504773A GB1406336A GB 1406336 A GB1406336 A GB 1406336A GB 2504773 A GB2504773 A GB 2504773A GB 2504773 A GB2504773 A GB 2504773A GB 1406336 A GB1406336 A GB 1406336A
Authority
GB
United Kingdom
Prior art keywords
tin
radical
weight
paper pulp
polymers
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
GB2504773A
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.)
Rhone Poulenc SA
Original Assignee
Rhone Poulenc SA
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 Rhone Poulenc SA filed Critical Rhone Poulenc SA
Publication of GB1406336A publication Critical patent/GB1406336A/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
    • D21H17/59Synthetic 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 silicon
    • 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
    • D21H17/55Polyamides; Polyaminoamides; Polyester-amides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Paper (AREA)
  • Silicon Polymers (AREA)
  • Developing Agents For Electrophotography (AREA)
  • Diaphragms For Electromechanical Transducers (AREA)

Abstract

1406336 Treatment of paper pulp RHONEPOULENC SA 25 May 1973 [26 May 1972] 25047/73 Heading D2B [Also in Division C3] Paper pulp is treated directly on a paper making machine with an aqueous emulsion containing at least one organosilicon polymer wherein the emulsion contains in an amount of 5-40% of the weight of the total organosilicon polymer content an organic condensate which can be cured for sizing the paper. The organic condensate is obtained by reacting (a) an amine type polymer containing units of the general formula: wherein X is an integer from 1 to 7, R is a hydrogen atom or an alkyl radical with 1 to 4 carbon atoms and may be the same or different in each C n H 2n NR group when X is greater than 2, and A is a divalent radical of the formula -CO-, -CS-, -CO-Q- or -CO-Q'-CO- in which Q is an alkylene radical with 2 to 6 carbon atoms and Q' is a saturated or unsaturated linear or branched, divalent organic radical; with (b) an epihalohydrin or a compound containing at least one halohydrin group. The organosilicon polymer can be chosen from (a) methylhydrogenopolysiloxanes of viscosity ranging from 2 cPo at 25‹C to 5000 cPo at 25‹C corresponding to the general formula in which R', which may be the same or different represents a methyl group or a hydrogen atom, a represents an integer in the range 3 to 600, and b represents zero or an integer in the range 1 to 200; (b) dimethylpolysiloxane oils and rubbers corresponding to the general formula in which R", which may be the same or different, represents a methyl group, a hydroxyl radical or a lower alkoxy radical with 1-4 carbon atoms, and c represents an integer in the range 5-20000; and (c) methylpolysiloxane resins which are liquid, solid or paste like products which may .be dissolved in toluene, xylene, cumene, cyclohexane, methylcyclohexane and alkenes with 5 to 20 carbon atoms. They are formed from a succession of units of formula SiO 2 , CH 3 SiO 1 . 5 , (CH 3 ) 2 SiO and (CH 3 ) 3 SiO 0 . 5 , which are distributed so that the resins possess 0.9 to 1.9 methyl group per silicon atom. They can further contain up to 25% by weight of hydroxyl and/or alkoxy groups such as methoxy, ethoxy, isoproxy, n-butoxy and isobutoxy groups bonded to silicon atoms. Emulsifying agents of an amount up to 20% of the weight of the organo silicon polymer may be used to facilitate emulsification of the polymers, possible agents including (1) non- ionic agents such as alkyl-phenyl monoethers of polyalkylene glycol, the products of the reaction between fatty alcohols of amides of fatty acids and ethylene oxide, and a polyvinyl alcohol and (2) cationic agents such as salts of aliphatic amines and quarternary ammonia, pyridinium salts which possess long hydrocarbon chains, and the products of the reaction of fatty acids with N, N-dialkyl-amino-alcohols. The curing of the organosilicon polymers which contain hydroxyl or alkoxy groups may be accelerated by the addition of catalysts of weight 0.1-80% that of the polymers. The catalysts are preferably added seperately to the paper pulp in the form of aqueous emulsions or solution. The catalysts used include metal and organometallic salts of carboxylic acids such as zinc, lead, cobalt, tin, iron and dialkyl-tin salts of carboxylic acids e.g. acetates, zinc, lead, tin, or iron 2-ethyl-hexanoate, dibutyl-tin dilaurate or dioctyl-tin dilaurate, dibutyl or dioctyl-tin diacetate and dibutyl-tin maleate; chelates prepared from beta-diketones or beta-keto-esters and metal derivatives such as iron and totanium acetylacetonates, alkyl titanates such as propyl, isopropyl, butyl, isobutyl, hexyl, 2-ethyl hexyl and octyl titinate; and complexes obtained by reacting alkyl titanates or titanium tetrachloride with carboxylic acid anhydrides or alkanolamines such as the titanates of acetic anhydride and of triethanolamine. When resinous organosilicon polymers are incorporated, they may be, prior to emulsification, dissolved in toluene, xylene, cyclohexane or methylcyclohexane. The paper pulp may be natural or regenerated cellulosic fibres and may originate from the wood of deciduous trees or conifers, from rags or from straw and may be bleached. Synthetic fibres may also be incorporated. The paper product preferbaly contains 0.1 to 3% by weight of organosilicon polymers, and possesses hydrophobic, non-stick and electrical insulating properties.
GB2504773A 1972-05-26 1973-05-25 Process for the treatment of paper pulp Expired GB1406336A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7218896A FR2186035A5 (en) 1972-05-26 1972-05-26

Publications (1)

Publication Number Publication Date
GB1406336A true GB1406336A (en) 1975-09-17

Family

ID=9099162

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2504773A Expired GB1406336A (en) 1972-05-26 1973-05-25 Process for the treatment of paper pulp

Country Status (13)

Country Link
JP (1) JPS4941620A (en)
AR (1) AR194559A1 (en)
BE (1) BE800090A (en)
BR (1) BR7303799D0 (en)
CA (1) CA980515A (en)
CH (1) CH565895A5 (en)
ES (1) ES415233A1 (en)
FI (1) FI55879C (en)
FR (1) FR2186035A5 (en)
GB (1) GB1406336A (en)
IT (1) IT987946B (en)
NL (1) NL7306999A (en)
NO (1) NO140637C (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4826415U (en) * 1971-08-04 1973-03-30
ATE132556T1 (en) * 1988-06-14 1996-01-15 Procter & Gamble GENTLE TISSUE PAPER

Also Published As

Publication number Publication date
NL7306999A (en) 1973-11-28
DE2326828B2 (en) 1976-09-23
FI55879C (en) 1979-10-10
FI55879B (en) 1979-06-29
DE2326828A1 (en) 1973-11-29
IT987946B (en) 1975-03-20
BR7303799D0 (en) 1974-01-17
BE800090A (en) 1973-11-26
JPS4941620A (en) 1974-04-19
CA980515A (en) 1975-12-30
FR2186035A5 (en) 1974-01-04
AR194559A1 (en) 1973-07-23
NO140637C (en) 1979-10-10
NO140637B (en) 1979-07-02
ES415233A1 (en) 1976-02-01
CH565895A5 (en) 1975-08-29

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee