GB1425371A - Electroconductive resin - Google Patents

Electroconductive resin

Info

Publication number
GB1425371A
GB1425371A GB2258573A GB2258573A GB1425371A GB 1425371 A GB1425371 A GB 1425371A GB 2258573 A GB2258573 A GB 2258573A GB 2258573 A GB2258573 A GB 2258573A GB 1425371 A GB1425371 A GB 1425371A
Authority
GB
United Kingdom
Prior art keywords
reacting
bis
tetramethyl
resins
electroconductive
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
GB2258573A
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.)
Monsanto Co
Original Assignee
Monsanto 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
Priority claimed from US252560A external-priority patent/US3887751A/en
Priority claimed from US00253016A external-priority patent/US3825511A/en
Application filed by Monsanto Co filed Critical Monsanto Co
Publication of GB1425371A publication Critical patent/GB1425371A/en
Expired legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/10—Bases for charge-receiving or other layers
    • G03G5/105—Bases for charge-receiving or other layers comprising electroconductive macromolecular compounds
    • G03G5/107—Bases for charge-receiving or other layers comprising electroconductive macromolecular compounds the electroconductive macromolecular compounds being cationic
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02—Polyamines
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02—Polyamines
    • C08G73/0206—Polyalkylene(poly)amines
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02—Polyamines
    • C08G73/0206—Polyalkylene(poly)amines
    • C08G73/0213—Preparatory process
    • C08G73/0226—Quaternisation of polyalkylene(poly)amines
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L29/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
    • C08L29/02—Homopolymers or copolymers of unsaturated alcohols
    • C08L29/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
    • C08L79/02—Polyamines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Physics & Mathematics (AREA)
  • Photoreceptors In Electrophotography (AREA)
  • Laminated Bodies (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

1425371 Electroconductive resins MONSANTO CO 11 May 1973 [12 May 1972 15 May 1972] 22585/73 Headings C3R and C3P An electroconductive resin for use in electrographic printing processes is obtained by reacting a di-(tertiary amine) or a poly-(tertiary amine) or a mixture thereof with a 1,4-dihaloalkene-2- or a 1,4-dihalocycloalkene-2. In examples resins are prepared by reacting 1,4- dichlorobutene-2 with 1,3-bis-(dimethylamino)- 2-hydroxypropane, with triethylenediamine, with N,N,N<SP>1</SP>,N<SP>1</SP>-tetramethyl p-xylylene diamine, with a mixture of 1,3-bis-(dimethylamino)-2-hydroxypropane and 2,4,6-tris- (dimethylaminomethyl) - phenol, with 1,4- bis - (diethylamino) - butene - 2 and with 1,4-dipiperidyl-butene-2; by reacting 1,4- dibromobutene-2- with N,N,N<SP>1</SP>,N<SP>1</SP>-tetramethyl ethylene diamine; by reacting 1,4- dichlorocyclopentene-2 with N,N<SP>1</SP>-dimethylpiperazine; by reacting 1,4-dichloropentene-2 with N,N,N<SP>1</SP>,N<SP>1</SP>-tetrakis-(hydroxyethyl)ethylene diamine; by reacting 1,4-dichloro-2-methylbutene-2 with N,N,N<SP>1</SP>,N<SP>1</SP>-tetramethyl hexylenediamine and by reacting 1,4-dichlorohexene-2 with N,N,N<SP>1</SP>,N<SP>1</SP>-tetrabutylethylenediamine; aqueous solutions of some of the resins, alone and mixed with polyvinyl alcohol, polyvinyl acetate and with hydroxyethylated starch, are applied to paper and dried to obtain electroconductive coatings.
GB2258573A 1972-05-12 1973-05-11 Electroconductive resin Expired GB1425371A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US252560A US3887751A (en) 1972-05-12 1972-05-12 Electroconductive sheet material and process of preparation
US00253016A US3825511A (en) 1972-05-15 1972-05-15 Electroconductive resins and process of preparation

Publications (1)

Publication Number Publication Date
GB1425371A true GB1425371A (en) 1976-02-18

Family

ID=26942437

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2258573A Expired GB1425371A (en) 1972-05-12 1973-05-11 Electroconductive resin

Country Status (8)

Country Link
CA (1) CA1010191A (en)
CH (1) CH576160A5 (en)
DE (1) DE2323886A1 (en)
FR (1) FR2184737B1 (en)
GB (1) GB1425371A (en)
IT (1) IT987393B (en)
NL (1) NL7306453A (en)
SE (1) SE385742B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116410464A (en) * 2023-04-14 2023-07-11 湖南大学 Main chain cationic polymer capable of being click chemically modified and preparation method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4305829A (en) 1979-06-29 1981-12-15 Union Carbide Corporation Process for flocculating an aqueous suspension of particles with quaternary ammonium graft copolymers

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116410464A (en) * 2023-04-14 2023-07-11 湖南大学 Main chain cationic polymer capable of being click chemically modified and preparation method thereof

Also Published As

Publication number Publication date
CH576160A5 (en) 1976-05-31
FR2184737A1 (en) 1973-12-28
SE385742B (en) 1976-07-19
CA1010191A (en) 1977-05-10
IT987393B (en) 1975-02-20
NL7306453A (en) 1973-11-14
DE2323886A1 (en) 1973-11-22
FR2184737B1 (en) 1977-04-29

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Legal Events

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