GB1355122A – Method for production of cationic surfactant
– Google Patents
GB1355122A – Method for production of cationic surfactant
– Google Patents
Method for production of cationic surfactant
Info
Publication number
GB1355122A
GB1355122A
GB4784571A
GB4784571A
GB1355122A
GB 1355122 A
GB1355122 A
GB 1355122A
GB 4784571 A
GB4784571 A
GB 4784571A
GB 4784571 A
GB4784571 A
GB 4784571A
GB 1355122 A
GB1355122 A
GB 1355122A
Authority
GB
United Kingdom
Prior art keywords
polycondensate
chlorinated
water
naphthalene
polycondensates
Prior art date
1970-10-17
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
GB4784571A
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.)
Kureha Corp
Kurita Water Industries Ltd
Original Assignee
Kureha Corp
Kurita Water Industries Ltd
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.)
1970-10-17
Filing date
1971-10-14
Publication date
1974-06-05
1971-10-14
Application filed by Kureha Corp, Kurita Water Industries Ltd
filed
Critical
Kureha Corp
1974-06-05
Publication of GB1355122A
publication
Critical
patent/GB1355122A/en
Status
Expired
legal-status
Critical
Current
Links
Espacenet
Global Dossier
Discuss
239000003093
cationic surfactant
Substances
0.000
title
1
238000004519
manufacturing process
Methods
0.000
title
1
WSFSSNUMVMOOMR-UHFFFAOYSA-N
Formaldehyde
Chemical compound
O=C
WSFSSNUMVMOOMR-UHFFFAOYSA-N
0.000
abstract
6
CXWXQJXEFPUFDZ-UHFFFAOYSA-N
tetralin
Chemical compound
C1=CC=C2CCCCC2=C1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N
0.000
abstract
3
YGYNBBAUIYTWBF-UHFFFAOYSA-N
2,6-dimethylnaphthalene
Chemical compound
C1=C(C)C=CC2=CC(C)=CC=C21
YGYNBBAUIYTWBF-UHFFFAOYSA-N
0.000
abstract
2
QIMMUPPBPVKWKM-UHFFFAOYSA-N
2-methylnaphthalene
Chemical compound
C1=CC=CC2=CC(C)=CC=C21
QIMMUPPBPVKWKM-UHFFFAOYSA-N
0.000
abstract
2
JUJWROOIHBZHMG-UHFFFAOYSA-N
Pyridine
Chemical compound
C1=CC=NC=C1
JUJWROOIHBZHMG-UHFFFAOYSA-N
0.000
abstract
2
238000005189
flocculation
Methods
0.000
abstract
2
IVSZLXZYQVIEFR-UHFFFAOYSA-N
m-xylene
Chemical group
CC1=CC=CC(C)=C1
IVSZLXZYQVIEFR-UHFFFAOYSA-N
0.000
abstract
2
UMGDCJDMYOKAJW-UHFFFAOYSA-N
thiourea
Chemical compound
NC(N)=S
UMGDCJDMYOKAJW-UHFFFAOYSA-N
0.000
abstract
2
XLYOFNOQVPJJNP-UHFFFAOYSA-N
water
Substances
O
XLYOFNOQVPJJNP-UHFFFAOYSA-N
0.000
abstract
2
UKAMWVYNAVUZEA-UHFFFAOYSA-N
2-butylnaphthalene
Chemical compound
C1=CC=CC2=CC(CCCC)=CC=C21
UKAMWVYNAVUZEA-UHFFFAOYSA-N
0.000
abstract
1
239000005995
Aluminium silicate
Substances
0.000
abstract
1
XSQUKJJJFZCRTK-UHFFFAOYSA-N
Urea
Natural products
NC(N)=O
XSQUKJJJFZCRTK-UHFFFAOYSA-N
0.000
abstract
1
239000011149
active material
Substances
0.000
abstract
1
125000002723
alicyclic group
Chemical group
0.000
abstract
1
235000012211
aluminium silicate
Nutrition
0.000
abstract
1
WLDHEUZGFKACJH-UHFFFAOYSA-K
amaranth
Chemical compound
[Na+].[Na+].[Na+].C12=CC=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(O)=C1N=NC1=CC=C(S([O-])(=O)=O)C2=CC=CC=C12
WLDHEUZGFKACJH-UHFFFAOYSA-K
0.000
abstract
1
-1
amino compound
Chemical class
0.000
abstract
1
150000004945
aromatic hydrocarbons
Chemical class
0.000
abstract
1
125000002091
cationic group
Chemical group
0.000
abstract
1
125000001309
chloro group
Chemical group
Cl*
0.000
abstract
1
230000003311
flocculating effect
Effects
0.000
abstract
1
230000016615
flocculation
Effects
0.000
abstract
1
125000004435
hydrogen atom
Chemical group
[H]*
0.000
abstract
1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N
kaolin
Chemical compound
O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O
NLYAJNPCOHFWQQ-UHFFFAOYSA-N
0.000
abstract
1
125000002496
methyl group
Chemical group
[H]C([H])([H])*
0.000
abstract
1
229920000642
polymer
Polymers
0.000
abstract
1
125000002924
primary amino group
Chemical group
[H]N([H])*
0.000
abstract
1
UMJSCPRVCHMLSP-UHFFFAOYSA-N
pyridine
Natural products
COC1=CC=CN=C1
UMJSCPRVCHMLSP-UHFFFAOYSA-N
0.000
abstract
1
239000007858
starting material
Substances
0.000
abstract
1
239000000725
suspension
Substances
0.000
abstract
1
Classifications
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
C08G10/00—Condensation polymers of aldehydes or ketones with aromatic hydrocarbons or halogenated aromatic hydrocarbons only
C08G10/02—Condensation polymers of aldehydes or ketones with aromatic hydrocarbons or halogenated aromatic hydrocarbons only of aldehydes
C08G10/04—Chemically-modified polycondensates
Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
Y10S516/07—Organic amine, amide, or n-base containing
Abstract
1355122 Flocculating KUREHA KAGAKU KOGYO KK and KURITA WATER INDUSTRIES Ltd 14 Oct 1971 [17 Oct 1970] 47845/71 Heading C1C [Also in Division C3] Polymers which are water-soluble, cationic surface-active materials for use in flocculation processes are obtained by (i) condensing formaldehyde with an aromatic hydrocarbon having methyl substituents or side-chains or alicyclic structures containing hydrogen atoms capable of being replaced by chlorine atoms, to obtain a polycondensate, (ii) chlorinating the polycondensate and (iii) reacting the chlorinated polycondensate with an amino compound. In examples m-xylene, 2-methyl naphthalene, 2,6- dimethyl naphthalene, 2-butyl naphthalene and tetralin are condensed with p-formaldehyde and formalin, the polycondensates are chlorinated, and the chlorinated polycondensates are then reacted with thiourea and pyridine. Other starting materials and amino compounds are mentioned. In examples flocculation in water is demonstrated with suspensions of kaolin and solutions of Amaranth red.
GB4784571A
1970-10-17
1971-10-14
Method for production of cationic surfactant
Expired
GB1355122A
(en)
Applications Claiming Priority (1)
Application Number
Priority Date
Filing Date
Title
JP45090961A
JPS4814792B1
(en)
1970-10-17
1970-10-17
Publications (1)
Publication Number
Publication Date
GB1355122A
true
GB1355122A
(en)
1974-06-05
Family
ID=14013077
Family Applications (1)
Application Number
Title
Priority Date
Filing Date
GB4784571A
Expired
GB1355122A
(en)
1970-10-17
1971-10-14
Method for production of cationic surfactant
Country Status (5)
Country
Link
US
(1)
US3904687A
(en)
JP
(1)
JPS4814792B1
(en)
CA
(1)
CA963196A
(en)
DE
(1)
DE2151523A1
(en)
GB
(1)
GB1355122A
(en)
Families Citing this family (4)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
DE2935776A1
(en)
*
1979-09-05
1981-04-16
Theodor Prof. Dr. 4400 Münster Eckert
Indomethacin, naproxen and diclofenac salts – with organic bases, esp. di:ethylamine, tri:ethanol-amine or tri:ethylamine
DE19752092A1
(en)
*
1997-11-25
1999-06-02
Clariant Gmbh
New crystal modification of thiazine indigo
US8648152B2
(en)
*
2007-11-16
2014-02-11
Mitsubishi Gas Chemical Company, Inc.
Polyfunctional dimethylnaphthalene formaldehyde resin, and process for production thereof
EP2821176A1
(en)
2013-07-02
2015-01-07
Siemens VAI Metals Technologies GmbH
Device for moving an arrangement for cutting and welding metal strips ; Methof of cutting and welding using such device
1970
1970-10-17
JP
JP45090961A
patent/JPS4814792B1/ja
active
Pending
1971
1971-10-14
GB
GB4784571A
patent/GB1355122A/en
not_active
Expired
1971-10-15
CA
CA125,230A
patent/CA963196A/en
not_active
Expired
1971-10-15
DE
DE19712151523
patent/DE2151523A1/en
active
Pending
1971-10-18
US
US190356A
patent/US3904687A/en
not_active
Expired – Lifetime
Also Published As
Publication number
Publication date
DE2151523A1
(en)
1972-06-29
CA963196A
(en)
1975-02-18
US3904687A
(en)
1975-09-09
JPS4814792B1
(en)
1973-05-10
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Legal Events
Date
Code
Title
Description
1974-10-09
PS
Patent sealed [section 19, patents act 1949]
1977-05-18
PLNP
Patent lapsed through nonpayment of renewal fees
