GB1035876A - Paper sizing - Google Patents

Paper sizing

Info

Publication number
GB1035876A
GB1035876A GB3334964A GB3334964A GB1035876A GB 1035876 A GB1035876 A GB 1035876A GB 3334964 A GB3334964 A GB 3334964A GB 3334964 A GB3334964 A GB 3334964A GB 1035876 A GB1035876 A GB 1035876A
Authority
GB
United Kingdom
Prior art keywords
parts
water
mixture
emulsified
formaldehyde
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
GB3334964A
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.)
Bayer AG
Original Assignee
Bayer AG
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 Bayer AG filed Critical Bayer AG
Publication of GB1035876A publication Critical patent/GB1035876A/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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paper (AREA)
  • Silicon Polymers (AREA)

Abstract

Emulsions of organopolysiloxanes, for use in sizing paper (see Division D2), are made as follows: (A) a 94/6 mixture of methylhydrogendichlorosilan and trimethylmonochlorosilane is hydrolysed to give an oil of 20 cS viscosity, octamethyl-cyclotetrasiloxane is treated with bleaching earth and heated at 120 DEG C. to a viscosity of 1000 cS, then two oils are mixed in equal amounts and emulsified in water with cetylbenzyldimethyl-ammonium chloride, glycocoll and hydrochloric acid; (B) a 90/10 mixture of methylhydrogendichlorosilane and trimethylchlorosilane is hydrolysed to a thinly liquid oil, which is emulsified in water with dodecylamine, tetrabromoethane, aminocaproic acid and hydrochloric acid; (C) 9 parts of methyltrichlorosilane, 1 part of dimethyldichlorosilane, 8 parts of toluene and 2 parts of n-butanol are added to a mixture of 40 parts of water and 20 parts of toluene, a silicone-resin solution is obtained by hydrolysis and subsequent neutralization with sodium bicarbonate, solvent is distilled off to 50% solids, 36 parts of the silicone oil B are mixed with 8 parts of this solution and emulsified in water with cetylbenzyldimethylammonium chloride, glutamic acid and hydrochloric acid; (D) a mixture of 60.4 parts of methylhydrogendichlorosilane, 34.6 parts of dimethyldichlorosilane and 5 parts of trimethylmonochlorosilane is hydrolysed to a thin oil, which is emulsified in water with cetylbenzyldimethylammonium chloride, hydrochloric acid and aminopropionic acid; and (E) an equimolar mixture of methyltrichlorosilane, dimethyldichlorosilane, phenyltrichlorosilane and diphenyldichlorosilane is hydrolysed in a mixture of water, butanol and cyclohexanol, the product washed with water and concentrated to 50% by distilling off solvent, 38 parts of silicone oil B are mixed with 4 parts of this resin solution and emulsified in water with dodecylamine, tetrabromoethane, glycocoll and hydrochloric acid.ALSO:Paper is sized by adding to the pulp an aqueous emulsion of linear organopolysiloxane in which the end units are R2 (OH)SiO 1/2 , (CH3)2 (H)SiO 1/2 or (CH3)3SiO 1/2 , 50 to 100% of the siloxane units are R(H)SiO, and all remaining units are R2SiO, in which formulae each R is alkyl or aryl, in amount equivalent of 0.01 to 5 parts of organosiloxane by weight per hundred parts of air-dried cellulose pulp. The linear organopolysiloxane may be mixed with up to 10% by weight of a cross-linked or branched organopolysiloxane of units RSiO 3/2 and R2SiO. The emulsifier in the emulsion may be of the cation-active type. The emulsion may also contain a metal salt, e.g. dibutyltin dilaurate, dioctyltin dimaleate or compounds of lead, cobalt, zinc, titanium or cerium, to accelerate cure or a watersoluble prepolymer of a synthetic resin, e.g. polyethyleneimine, urea-formaldehyde, melamineformaldehyde, ethyleneurea-formaldehyde, N-alkylurea-formaldehyde, guaridine-formaldehyde, dicyandiamide-formaldehyde, epoxide resin or a product of reaction of a polyamine with epichlorohydrin, dichlorohydrin or an epoxide resin. Fillers may be incorporated in the pulp, e.g. kaolin, calcium silicate, calcium sulphate, barium sulphate, talc, chalk, titanium dioxide, zinc sulphide or amorphous silica.
GB3334964A 1963-08-16 1964-08-14 Paper sizing Expired GB1035876A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF0040504 1963-08-16

Publications (1)

Publication Number Publication Date
GB1035876A true GB1035876A (en) 1966-07-13

Family

ID=7098258

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3334964A Expired GB1035876A (en) 1963-08-16 1964-08-14 Paper sizing

Country Status (5)

Country Link
BE (1) BE651846A (en)
DE (1) DE1546248A1 (en)
GB (1) GB1035876A (en)
LU (1) LU46625A1 (en)
NL (1) NL6409346A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1088939A1 (en) * 1999-09-29 2001-04-04 Dow Corning Toray Silicone Co., Ltd. Printing paper sizing agent composition
CN103204993A (en) * 2013-04-16 2013-07-17 江苏大学 Preparation method of methyl silicone resin
CN103204994A (en) * 2013-04-16 2013-07-17 江苏大学 Preparation method of phenyl silicon resin

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1088939A1 (en) * 1999-09-29 2001-04-04 Dow Corning Toray Silicone Co., Ltd. Printing paper sizing agent composition
CN103204993A (en) * 2013-04-16 2013-07-17 江苏大学 Preparation method of methyl silicone resin
CN103204994A (en) * 2013-04-16 2013-07-17 江苏大学 Preparation method of phenyl silicon resin
CN103204993B (en) * 2013-04-16 2015-06-10 江苏大学 Preparation method of methyl silicone resin

Also Published As

Publication number Publication date
NL6409346A (en) 1965-02-17
BE651846A (en) 1964-12-01
DE1546248A1 (en) 1969-07-17
LU46625A1 (en) 1964-09-28

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