DE2908965A1 - Verfahren zur herstellung eines kationischen polychloroprenlatex sowie seine abmischung mit bitumenemulsion - Google Patents

Verfahren zur herstellung eines kationischen polychloroprenlatex sowie seine abmischung mit bitumenemulsion

Info

Publication number: DE2908965A1
Authority: DE; Germany
Prior art keywords: weight; parts; tin; cationic; polychloroprene latex
Prior art date: 1979-03-07
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 Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

DE19792908965

Other languages

German (de)

English (en)

Inventor

Heinz Dipl Chem Dr Esser

Wilfried Dipl Chem Dr Nolte

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.)

1979-03-07

Filing date

1979-03-07

Publication date

1980-09-18

1979-03-07 Application filed by Bayer AG filed Critical Bayer AG

1979-03-07 Priority to DE19792908965 priority Critical patent/DE2908965A1/de

1980-02-26 Priority to DE8080100935T priority patent/DE3060121D1/de

1980-02-26 Priority to EP80100935A priority patent/EP0015477B1/de

1980-03-05 Priority to CA000347018A priority patent/CA1153143A/en

1980-03-05 Priority to JP2681180A priority patent/JPS55118908A/ja

1980-09-18 Publication of DE2908965A1 publication Critical patent/DE2908965A1/de

1981-06-18 Priority to US06/274,819 priority patent/US4340518A/en

Status Withdrawn legal-status Critical Current

Links

239000010426 asphalt Substances 0.000 title claims description 29
239000000839 emulsion Substances 0.000 title claims description 26
239000004816 latex Substances 0.000 title claims description 24
229920001084 poly(chloroprene) Polymers 0.000 title claims description 22
238000004519 manufacturing process Methods 0.000 title claims description 9
238000002156 mixing Methods 0.000 title claims description 8
229920000126 latex Polymers 0.000 claims description 34
239000003995 emulsifying agent Substances 0.000 claims description 20
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 19
125000002091 cationic group Chemical group 0.000 claims description 19
238000006116 polymerization reaction Methods 0.000 claims description 15
239000000178 monomer Substances 0.000 claims description 13
YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 claims description 12
239000000203 mixture Substances 0.000 claims description 12
238000000034 method Methods 0.000 claims description 10
150000001447 alkali salts Chemical class 0.000 claims description 8
150000001735 carboxylic acids Chemical class 0.000 claims description 8
150000003863 ammonium salts Chemical class 0.000 claims description 3
150000007522 mineralic acids Chemical class 0.000 claims description 2
150000007524 organic acids Chemical class 0.000 claims 1
235000005985 organic acids Nutrition 0.000 claims 1
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 22
150000003839 salts Chemical class 0.000 description 9
239000001632 sodium acetate Substances 0.000 description 7
235000017281 sodium acetate Nutrition 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 6
125000004432 carbon atom Chemical group C* 0.000 description 5
239000011734 sodium Substances 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 4
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 4
-1 alkali metal salt Chemical class 0.000 description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
230000029142 excretion Effects 0.000 description 4
NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 4
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
BITAPBDLHJQAID-KTKRTIGZSA-N 2-[2-hydroxyethyl-[(z)-octadec-9-enyl]amino]ethanol Chemical compound CCCCCCCC\C=C/CCCCCCCCN(CCO)CCO BITAPBDLHJQAID-KTKRTIGZSA-N 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
229960002089 ferrous chloride Drugs 0.000 description 3
150000003242 quaternary ammonium salts Chemical class 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 2
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Chemical class 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
150000001342 alkaline earth metals Chemical class 0.000 description 2
238000010276 construction Methods 0.000 description 2
WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 2
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 2
238000004945 emulsification Methods 0.000 description 2
235000019253 formic acid Nutrition 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
239000003999 initiator Substances 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
150000001451 organic peroxides Chemical class 0.000 description 2
235000006408 oxalic acid Nutrition 0.000 description 2
229920000768 polyamine Polymers 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011591 potassium Substances 0.000 description 2
235000019260 propionic acid Nutrition 0.000 description 2
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
239000011435 rock Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
230000006641 stabilisation Effects 0.000 description 2
238000011105 stabilization Methods 0.000 description 2
239000003784 tall oil Substances 0.000 description 2
QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
DEXFNLNNUZKHNO-UHFFFAOYSA-N 6-[3-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-3-oxopropyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)C(CCC1=CC2=C(NC(O2)=O)C=C1)=O DEXFNLNNUZKHNO-UHFFFAOYSA-N 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
208000009043 Chemical Burns Diseases 0.000 description 1
229910021577 Iron(II) chloride Inorganic materials 0.000 description 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
206010047700 Vomiting Diseases 0.000 description 1
235000011054 acetic acid Nutrition 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000002318 adhesion promoter Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000005210 alkyl ammonium group Chemical group 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
159000000009 barium salts Chemical class 0.000 description 1
239000002585 base Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001734 carboxylic acid salts Chemical class 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
239000003505 polymerization initiator Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229910052712 strontium Inorganic materials 0.000 description 1
CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
239000013589 supplement Substances 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
239000012209 synthetic fiber Substances 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
238000005496 tempering Methods 0.000 description 1
150000003628 tricarboxylic acids Chemical class 0.000 description 1
XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Natural products NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 1
230000008673 vomiting Effects 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F36/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F36/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F36/04—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F36/14—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated containing elements other than carbon and hydrogen
- C08F36/16—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated containing elements other than carbon and hydrogen containing halogen
- C08F36/18—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated containing elements other than carbon and hydrogen containing halogen containing chlorine
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L95/00—Compositions of bituminous materials, e.g. asphalt, tar, pitch
- C08L95/005—Aqueous compositions, e.g. emulsions

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Civil Engineering (AREA)
Materials Engineering (AREA)
Structural Engineering (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Polymerisation Methods In General (AREA)
Compositions Of Macromolecular Compounds (AREA)

DE19792908965 1979-03-07 1979-03-07 Verfahren zur herstellung eines kationischen polychloroprenlatex sowie seine abmischung mit bitumenemulsion Withdrawn DE2908965A1 (de)

Priority Applications (6)

Application Number	Priority Date	Filing Date	Title
DE19792908965 DE2908965A1 (de)	1979-03-07	1979-03-07	Verfahren zur herstellung eines kationischen polychloroprenlatex sowie seine abmischung mit bitumenemulsion
DE8080100935T DE3060121D1 (en)	1979-03-07	1980-02-26	Process for preparing a cationic polychloroprene latex and its mixture with a bituminous emulsion
EP80100935A EP0015477B1 (de)	1979-03-07	1980-02-26	Verfahren zur Herstellung eines kationischen Polychloroprenlatex sowie seine Abmischung mit Bitumenemulsion
CA000347018A CA1153143A (en)	1979-03-07	1980-03-05	Process for the production of a cationic polychloroprene latex and a mixture of this latex with bitumen emulsion
JP2681180A JPS55118908A (en)	1979-03-07	1980-03-05	Manufacture of cationic polychloroprene latex
US06/274,819 US4340518A (en)	1979-03-07	1981-06-18	Process for the production of a cationic polychloroprene latex and a mixture of this latex with bitumen emulsion

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19792908965 DE2908965A1 (de)	1979-03-07	1979-03-07	Verfahren zur herstellung eines kationischen polychloroprenlatex sowie seine abmischung mit bitumenemulsion

Publications (1)

Publication Number	Publication Date
DE2908965A1 true DE2908965A1 (de)	1980-09-18

Family

ID=6064759

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DE19792908965 Withdrawn DE2908965A1 (de)	1979-03-07	1979-03-07	Verfahren zur herstellung eines kationischen polychloroprenlatex sowie seine abmischung mit bitumenemulsion
DE8080100935T Expired DE3060121D1 (en)	1979-03-07	1980-02-26	Process for preparing a cationic polychloroprene latex and its mixture with a bituminous emulsion

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
DE8080100935T Expired DE3060121D1 (en)	1979-03-07	1980-02-26	Process for preparing a cationic polychloroprene latex and its mixture with a bituminous emulsion

Country Status (5)

Country	Link
US (1)	US4340518A (2)
EP (1)	EP0015477B1 (2)
JP (1)	JPS55118908A (2)
CA (1)	CA1153143A (2)
DE (2)	DE2908965A1 (2)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2517317B1 (fr) *	1981-11-27	1986-05-09	Elf France	Emulsions cationiques de liants bitumineux du type bitume-polymere et procede pour leur preparation
US4888368A (en) *	1988-05-12	1989-12-19	Dow Corning Corporation	Method of inhibiting the discoloration of emulsions and discoloration resistant emulsion compositions
US5087652A (en) *	1989-06-30	1992-02-11	E. I. Du Pont De Nemours And Company	Asphalt blends with chloroprene polymers or copolymers thereof with dichlorobutadiene
US5691033A (en) *	1995-06-07	1997-11-25	Reynolds Metals Company	Coating compositions containing aluminum pigment and methods of coating
CN101580562B (zh) *	2009-06-11	2010-12-08	山西合成橡胶集团有限责任公司	高转化率的高旋转粘度氯丁橡胶的制备方法
CN103819348B (zh) *	2014-03-10	2015-12-02	吉林恒升化工有限公司	脂肪胺聚氧乙烯醚阳离子沥青乳化剂及制备方法及用途
CN107849304B (zh)	2015-08-07	2020-12-11	性能材料北美股份有限公司	使用亚磷酸的改性沥青

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3890261A (en) *	1972-11-09	1975-06-17	Petro Tex Chem Corp	High solids chloroprene polymer latex
JPS5313216B2 (2) *	1973-06-29	1978-05-09
JPS5153587A (2) *	1974-11-06	1976-05-12	Toyo Soda Mfg Co Ltd
DE2520339C2 (de) *	1975-05-07	1984-12-20	Bayer Ag, 5090 Leverkusen	Verfahren zur Herstellung konzentrierter Polychloropren-Latices

1979
- 1979-03-07 DE DE19792908965 patent/DE2908965A1/de not_active Withdrawn
1980
- 1980-02-26 DE DE8080100935T patent/DE3060121D1/de not_active Expired
- 1980-02-26 EP EP80100935A patent/EP0015477B1/de not_active Expired
- 1980-03-05 CA CA000347018A patent/CA1153143A/en not_active Expired
- 1980-03-05 JP JP2681180A patent/JPS55118908A/ja active Granted
1981
- 1981-06-18 US US06/274,819 patent/US4340518A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
JPS6255525B2 (2)	1987-11-20
CA1153143A (en)	1983-08-30
EP0015477B1 (de)	1981-12-30
JPS55118908A (en)	1980-09-12
US4340518A (en)	1982-07-20
EP0015477A1 (de)	1980-09-17
DE3060121D1 (en)	1982-02-18

Legal Events

Date	Code	Title	Description
1983-01-27	8130	Withdrawal

Publication	Publication Date	Title
DE2066160C2 (de)	1985-07-11	Selbstvernetzendes Polymerisat, Verfahren zu seiner Herstellung und seine Verwendung zur Behandlung von Papier
DE4213154C1 (2)	1993-06-17
DE1520543C3 (de)	1973-12-06	Verfahren zur Herstellung von hartbaren elastomeren Tetrafluorathylen mischpolymerisaten
DE1495645B2 (de)	1974-03-28	Verfahren zur Herstellung stabiler, wäßriger Emulsionen bzw. Dispersionen von Äthylen-Mischpolymerisaten
DE2010763A1 (de)	1970-10-08	Kationische synthetische Kautschuklatexe und Verfahren zu deren Herstellung
DE69220356T2 (de)	1997-10-23	Hochwetterbeständige einkomponentartige vernetzbare emulsion
DE2431393A1 (de)	1975-01-30	Latex-asphalt-emulsionsmasse und verfahren zur herstellung derselben
DE2361544A1 (de)	1975-06-19	Papierleimungsmittel
EP0015477B1 (de)	1981-12-30	Verfahren zur Herstellung eines kationischen Polychloroprenlatex sowie seine Abmischung mit Bitumenemulsion
DE3620149A1 (de)	1987-12-17	Geruchsarmes wasserloesliches polymerisat oder copolymerisat, seine herstellung und verwendung
EP0025979A1 (de)	1981-04-01	Wässrige Lösung oder Dispersion eines Styrol/Maleinsäureanhydrid-Copolymers, Verfahren zu ihrer Herstellung und ihre Verwendung
DE2550572A1 (de)	1976-05-20	Verfahren zur herstellung fluessiger harzmassen
EP0529695A2 (de)	1993-03-03	Verfahren zur Herstellung von Polymerdispersionen
DE1595051B2 (de)	1972-05-18	Verfahren zur herstellung von polyaminsulfonen
EP0001868B1 (de)	1982-12-15	Papierleimungsmittel
DE1103569B (de)	1961-03-30	Fuer die Herstellung von geformten Gebilden geeignete waessrige Dispersionen von synthetischen Elastomeren
EP0647658B1 (en)	1998-11-18	Improvements in or relating to ethylene based emulsion polymers
EP0238930B1 (de)	1989-10-18	Neue Sulfonsäuregruppen enthaltende Melamin-Formaldehyd-Kondensationsprodukte, Verfahren zu ihrer Herstellung und deren Verwendung.
DE1137217B (de)	1962-09-27	Verfahren zur Herstellung kationaktiver Latices
DE965568C (de)	1957-06-13	Verfahren zur Behandlung von Boeden
DE69406527T2 (de)	1998-06-04	Acrylat kautschuk zusammensetzung
DE1902631C3 (de)	1978-08-10	Vulkanisierbare Massen für die Herstellung von elastomeren vulkanisierten Formkörpern
DE2512320A1 (de)	1975-09-25	Verfahren zur herstellung einer ueberzugsmasse
DE2143682A1 (de)	1973-03-08	Verfahren zur herstellung eines bestaendigen latex
DE69227377T2 (de)	1999-05-12	Stabilisierte wässrige lösung