NO333584B1 - In situ-fremgangsmate for fremstilling av kvaternaere ammoniumbikarbonater og kvaternaere ammoniumkarbonater - Google Patents

In situ-fremgangsmate for fremstilling av kvaternaere ammoniumbikarbonater og kvaternaere ammoniumkarbonater Download PDF

Info

Publication number: NO333584B1
Authority: NO; Norway
Prior art keywords: quaternary ammonium; carbonate; alkyl; methocarbonate; methanol
Prior art date: 2001-07-09

Application number

NO20040069A

Other languages

English (en)

Norwegian (no)

Other versions

NO78493A (no

NO20040069L (no

Inventor

Leigh E Walker

Original Assignee

Lonza 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.)

2001-07-09

Filing date

2004-01-08

Publication date

2013-07-15

2004-01-08 Application filed by Lonza Ag filed Critical Lonza Ag

2004-03-05 Publication of NO20040069L publication Critical patent/NO20040069L/no

2005-01-31 Publication of NO78493A publication Critical patent/NO78493A/no

2013-07-15 Publication of NO333584B1 publication Critical patent/NO333584B1/no

Links

125000001453 quaternary ammonium group Chemical group 0.000 title claims abstract description 77
238000000034 method Methods 0.000 title claims abstract description 71
239000001099 ammonium carbonate Substances 0.000 title claims abstract description 36
235000012538 ammonium bicarbonate Nutrition 0.000 title claims abstract description 19
238000002360 preparation method Methods 0.000 title claims abstract description 8
235000011162 ammonium carbonates Nutrition 0.000 title abstract description 15
238000011065 in-situ storage Methods 0.000 title abstract description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 150
238000006243 chemical reaction Methods 0.000 claims abstract description 37
239000000203 mixture Substances 0.000 claims abstract description 35
150000001412 amines Chemical class 0.000 claims abstract description 32
150000005676 cyclic carbonates Chemical class 0.000 claims abstract description 24
ATBNMWWDBWBAHM-UHFFFAOYSA-N n-decyl-n-methyldecan-1-amine Chemical compound CCCCCCCCCCN(C)CCCCCCCCCC ATBNMWWDBWBAHM-UHFFFAOYSA-N 0.000 claims description 36
JGFDZZLUDWMUQH-UHFFFAOYSA-N Didecyldimethylammonium Chemical compound CCCCCCCCCC[N+](C)(C)CCCCCCCCCC JGFDZZLUDWMUQH-UHFFFAOYSA-N 0.000 claims description 35
229940078672 didecyldimethylammonium Drugs 0.000 claims description 35
IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 claims description 33
RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical group CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 27
125000000217 alkyl group Chemical group 0.000 claims description 17
229910000013 Ammonium bicarbonate Inorganic materials 0.000 claims description 12
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
235000012501 ammonium carbonate Nutrition 0.000 claims description 9
KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical group O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
239000001257 hydrogen Substances 0.000 claims description 5
229910052739 hydrogen Inorganic materials 0.000 claims description 5
YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 claims description 5
125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 4
YJLYANLCNIKXMG-UHFFFAOYSA-N N-Methyldioctylamine Chemical compound CCCCCCCCN(C)CCCCCCCC YJLYANLCNIKXMG-UHFFFAOYSA-N 0.000 claims description 4
NAPSCFZYZVSQHF-UHFFFAOYSA-N dimantine Chemical compound CCCCCCCCCCCCCCCCCCN(C)C NAPSCFZYZVSQHF-UHFFFAOYSA-N 0.000 claims description 4
229950010007 dimantine Drugs 0.000 claims description 4
XTAZYLNFDRKIHJ-UHFFFAOYSA-N n,n-dioctyloctan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CCCCCCCC XTAZYLNFDRKIHJ-UHFFFAOYSA-N 0.000 claims description 4
VFLWKHBYVIUAMP-UHFFFAOYSA-N n-methyl-n-octadecyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCN(C)CCCCCCCCCCCCCCCCCC VFLWKHBYVIUAMP-UHFFFAOYSA-N 0.000 claims description 4
239000000376 reactant Substances 0.000 claims description 4
125000000923 (C1-C30) alkyl group Chemical group 0.000 claims description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 abstract description 11
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 abstract description 10
150000003512 tertiary amines Chemical class 0.000 abstract description 6
235000011114 ammonium hydroxide Nutrition 0.000 abstract description 5
-1 carbonate ester Chemical class 0.000 abstract description 5
150000003839 salts Chemical class 0.000 abstract description 3
229920003232 aliphatic polyester Polymers 0.000 abstract 2
150000002148 esters Chemical class 0.000 abstract 2
125000005910 alkyl carbonate group Chemical group 0.000 abstract 1
229920000515 polycarbonate Polymers 0.000 abstract 1
239000004417 polycarbonate Substances 0.000 abstract 1
238000010438 heat treatment Methods 0.000 description 33
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 24
238000004817 gas chromatography Methods 0.000 description 22
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 18
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
238000004519 manufacturing process Methods 0.000 description 10
150000003856 quaternary ammonium compounds Chemical class 0.000 description 7
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 6
230000015572 biosynthetic process Effects 0.000 description 5
239000000047 product Substances 0.000 description 5
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
238000004821 distillation Methods 0.000 description 4
150000002334 glycols Chemical class 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
239000000908 ammonium hydroxide Substances 0.000 description 3
229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 3
239000006227 byproduct Substances 0.000 description 3
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 3
MELGLHXCBHKVJG-UHFFFAOYSA-N dimethyl(dioctyl)azanium Chemical compound CCCCCCCC[N+](C)(C)CCCCCCCC MELGLHXCBHKVJG-UHFFFAOYSA-N 0.000 description 3
238000004090 dissolution Methods 0.000 description 3
239000002904 solvent Substances 0.000 description 3
ABVVEAHYODGCLZ-UHFFFAOYSA-N tridecan-1-amine Chemical compound CCCCCCCCCCCCCN ABVVEAHYODGCLZ-UHFFFAOYSA-N 0.000 description 3
PDSVZUAJOIQXRK-UHFFFAOYSA-N trimethyl(octadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)C PDSVZUAJOIQXRK-UHFFFAOYSA-N 0.000 description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
238000007792 addition Methods 0.000 description 2
235000019270 ammonium chloride Nutrition 0.000 description 2
239000001569 carbon dioxide Substances 0.000 description 2
229910002092 carbon dioxide Inorganic materials 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
239000007822 coupling agent Substances 0.000 description 2
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
VICYBMUVWHJEFT-UHFFFAOYSA-N dodecyltrimethylammonium ion Chemical compound CCCCCCCCCCCC[N+](C)(C)C VICYBMUVWHJEFT-UHFFFAOYSA-N 0.000 description 2
239000012467 final product Substances 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
230000007062 hydrolysis Effects 0.000 description 2
238000006460 hydrolysis reaction Methods 0.000 description 2
238000002386 leaching Methods 0.000 description 2
238000005259 measurement Methods 0.000 description 2
239000002184 metal Substances 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
ZUZLIXGTXQBUDC-UHFFFAOYSA-N methyltrioctylammonium Chemical compound CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC ZUZLIXGTXQBUDC-UHFFFAOYSA-N 0.000 description 2
238000005580 one pot reaction Methods 0.000 description 2
150000007530 organic bases Chemical class 0.000 description 2
239000003755 preservative agent Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
238000001577 simple distillation Methods 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
230000002528 anti-freeze Effects 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
229940090047 auto-injector Drugs 0.000 description 1
UDSAIICHUKSCKT-UHFFFAOYSA-N bromophenol blue Chemical compound C1=C(Br)C(O)=C(Br)C=C1C1(C=2C=C(Br)C(O)=C(Br)C=2)C2=CC=CC=C2S(=O)(=O)O1 UDSAIICHUKSCKT-UHFFFAOYSA-N 0.000 description 1
RBHJBMIOOPYDBQ-UHFFFAOYSA-N carbon dioxide;propan-2-one Chemical compound O=C=O.CC(C)=O RBHJBMIOOPYDBQ-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000001944 continuous distillation Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
150000001879 copper Chemical class 0.000 description 1
TXOJCSIIFFMREV-UHFFFAOYSA-L didecyl(dimethyl)azanium;carbonate Chemical compound [O-]C([O-])=O.CCCCCCCCCC[N+](C)(C)CCCCCCCCCC.CCCCCCCCCC[N+](C)(C)CCCCCCCCCC TXOJCSIIFFMREV-UHFFFAOYSA-L 0.000 description 1
229960004670 didecyldimethylammonium chloride Drugs 0.000 description 1
GUNDKLAGHABJDI-UHFFFAOYSA-N dimethyl carbonate;methanol Chemical compound OC.COC(=O)OC GUNDKLAGHABJDI-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910001510 metal chloride Inorganic materials 0.000 description 1
229910000000 metal hydroxide Inorganic materials 0.000 description 1
150000004692 metal hydroxides Chemical class 0.000 description 1
VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
YWWNNLPSZSEZNZ-UHFFFAOYSA-N n,n-dimethyldecan-1-amine Chemical compound CCCCCCCCCCN(C)C YWWNNLPSZSEZNZ-UHFFFAOYSA-N 0.000 description 1
AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
OMEMQVZNTDHENJ-UHFFFAOYSA-N n-methyldodecan-1-amine Chemical compound CCCCCCCCCCCCNC OMEMQVZNTDHENJ-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000002689 soil Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
238000004448 titration Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
- C07C209/14—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups
- C07C209/20—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups with formation of quaternary ammonium compounds

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Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Plural Heterocyclic Compounds (AREA)

NO20040069A 2001-07-09 2004-01-08 In situ-fremgangsmate for fremstilling av kvaternaere ammoniumbikarbonater og kvaternaere ammoniumkarbonater NO333584B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US30397101P	2001-07-09	2001-07-09
PCT/US2002/021236 WO2003006419A1 (en)	2001-07-09	2002-07-02	In situ process for preparing quaternary ammonium bicarbonates and quaternary ammonium carbonates

Publications (3)

Publication Number	Publication Date
NO20040069L NO20040069L (no)	2004-03-05
NO78493A NO78493A (no)	2005-01-31
NO333584B1 true NO333584B1 (no)	2013-07-15

Family

ID=23174485

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO20040069A NO333584B1 (no)	2001-07-09	2004-01-08	In situ-fremgangsmate for fremstilling av kvaternaere ammoniumbikarbonater og kvaternaere ammoniumkarbonater

Country Status (21)

Country	Link
US (2)	US6784307B2 (pl)
EP (1)	EP1406856B1 (pl)
JP (1)	JP4326327B2 (pl)
KR (1)	KR100886984B1 (pl)
CN (1)	CN100396660C (pl)
AT (1)	ATE466833T1 (pl)
AU (1)	AU2002316559B2 (pl)
BR (1)	BR0211229B1 (pl)
CA (1)	CA2453391C (pl)
DE (1)	DE60236286D1 (pl)
ES (1)	ES2345141T3 (pl)
HU (1)	HU230546B1 (pl)
MX (1)	MX244518B (pl)
NO (1)	NO333584B1 (pl)
NZ (1)	NZ530911A (pl)
PL (1)	PL205566B1 (pl)
RU (1)	RU2299193C2 (pl)
TW (1)	TWI242546B (pl)
UA (1)	UA76478C2 (pl)
WO (1)	WO2003006419A1 (pl)
ZA (1)	ZA200400698B (pl)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US20050003978A1 (en) *	2003-05-28	2005-01-06	Lonza Inc.	Quaternary ammonium carbonates and bicarbonates as anticorrosive agents
US20070260089A1 (en) *	2004-03-26	2007-11-08	Albemarle Corporation	Method for the Synthesis of Quaternary Ammonium Compounds and Compositions Thereof
US20070255074A1 (en) *	2004-03-26	2007-11-01	Sauer Joe D	Method for Exchanging Anions of Tetraalkylammonium Salts
MY148568A (en)	2004-12-09	2013-04-30	Lonza Ag	Quaternary ammonium salts as a conversion coating or coating enhancement
US20070167407A1 (en) *	2005-12-20	2007-07-19	Albemarle Corporation	Quaternary ammonium borate compositions and substrate preservative solutions containing them
US20070259781A1 (en) *	2006-05-08	2007-11-08	Sinha Rabindra K	Chemical formulations for removal of hazardous pollutants from combustion gases
US20080287331A1 (en) *	2007-05-18	2008-11-20	Hai-Hui Lin	Low voc cleaning composition for cleaning printing blankets and ink rollers
EP2374836A1 (en)	2010-04-07	2011-10-12	Nuplex Resins B.V.	Crosslinkable composition crosslinkable with a latent base catalyst.
CN101992055B (zh) *	2010-11-03	2013-09-11	天津大学	多釜串联连续合成四甲基铵碳酸盐的方法及装置
CN104039869B (zh)	2011-10-07	2016-04-27	树脂核动力工业有限公司	含潜在碱催化剂的可交联组合物及潜在的碱催化剂组合物
CN105985724A (zh) *	2011-10-07	2016-10-05	树脂核动力工业有限公司	可交联组合物
CN103111324B (zh) *	2013-01-25	2014-12-17	中南大学	含溴或碘的卤素盐的应用和合成甲基三长链脂肪烃基季铵盐衍生物的方法
JP6373965B2 (ja)	2013-04-08	2018-08-15	オールネックス・ネザーランズ・ビー．ブイ．ＡｌｌｎｅｘＮｅｔｈｅｒｌａｎｄｓＢ．Ｖ．	真マイケル付加（ｒｍａ）反応により架橋可能な組成物
GB2540066B (en)	2013-08-28	2017-06-14	Johnson Matthey Plc	Method of making a templating agent
JP6281280B2 (ja) *	2013-12-19	2018-02-21	東ソー株式会社	アロファネート・イソシアヌレート化触媒、該触媒を用いたポリイソシアネート組成物、該組成物の製造方法、及び該組成物を用いた二液型塗料組成物
US9677020B2 (en)	2014-06-25	2017-06-13	Afton Chemical Corporation	Hydrocarbyl soluble quaternary ammonium carboxylates and fuel compositions containing them
CA2983148C (en)	2015-04-17	2023-05-09	Allnex Netherlands B.V.	Process for the manufacture of a crosslinkable composition
CN107660227B (zh)	2015-04-17	2021-07-16	欧尼克斯荷兰有限公司	地板涂料组合物
EP3283584A1 (en)	2015-04-17	2018-02-21	Allnex Netherlands B.V.	A rma crosslinkable composition with improved adhesion
PL3283587T3 (pl)	2015-04-17	2024-07-22	Allnex Netherlands B.V.	Sieciowalne rma kompozycje i sieciowalne rma żywice do powłok łatwych do czyszczenia
CN104926668B (zh) *	2015-05-21	2018-02-27	北京盖雅环境科技有限公司	一种三长链烷基铵碳酸氢盐和碳酸盐的制备方法
IT201600130571A1 (it)	2016-12-23	2018-06-23	Lamberti Spa	Inibitori di idrati di gas
IT201600130556A1 (it)	2016-12-23	2018-06-23	Lamberti Spa	Inibitori di idrati di gas
CN107281994B (zh) *	2017-05-16	2019-08-27	天津大学	循环列管式反应器串联管式反应器制备四甲基碳酸氢铵的装置及方法
MY201814A (en)	2017-12-11	2024-03-19	Sherwin Williams Co	Method for making water-dispersible and water-dispersed polymers
CN108440306B (zh) *	2018-05-24	2023-11-03	柏川新材料科技(宁波)有限公司	一种四甲基碳酸铵的绿色生产的设备及方法
EP3663326A1 (en)	2018-12-04	2020-06-10	Allnex Netherlands B.V.	Rma crosslinkable polymer
KR102215414B1 (ko)	2020-07-07	2021-02-15	김상원	색상환
CN114570307A (zh) *	2022-03-18	2022-06-03	西安吉利电子新材料股份有限公司	一种从碳酸二甲酯直接生产电子级四甲基氢氧化铵制备系统及方法
CN116041187B (zh) *	2023-01-03	2025-06-06	烟台汉硅新材料科技有限公司	连续固定床催化反应原位制备混合甲胺碳酸盐的方法及其应用

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US264858A (en) *		1882-09-26		Bsek btjssey
US2635110A (en) *	1946-11-26	1953-04-14	Texas Co	Regeneration of hydrocarbon synthesis catalysts
US2635100A (en) *	1949-11-15	1953-04-14	Du Pont	Monoquaternary ammonium carbonates and their preparation
US3642858A (en)	1969-02-12	1972-02-15	Dow Chemical Co	Carbonate synthesis from alkylene carbonates
US3803201A (en) *	1971-02-22	1974-04-09	Dow Chemical Co	Synthesis of dimethyl carbonate
IT1034961B (it) *	1975-04-09	1979-10-10	Snam Progetti	Procedimento per la preparazione di dialchilcarbonati
DE2740243A1 (de) *	1977-09-07	1979-03-15	Bayer Ag	Verfahren zur herstellung von dialkylcarbonaten
JPS60100690A (ja) *	1983-11-02	1985-06-04	Tama Kagaku Kogyo Kk	水酸化第四アンモニウムの製造方法
GB8401919D0 (en) *	1984-01-25	1984-02-29	Bp Chem Int Ltd	Transesterification process
JPS61170588A (ja) *	1985-01-25	1986-08-01	Tama Kagaku Kogyo Kk	水酸化第四アンモニウム水溶液の製造方法
US4691041A (en) *	1986-01-03	1987-09-01	Texaco Inc.	Process for production of ethylene glycol and dimethyl carbonate
US4661609A (en) *	1986-07-31	1987-04-28	Texaco Inc.	Process for cosynthesis of ethylene glycol and dimethyl carbonate
US4776929A (en) *	1986-11-25	1988-10-11	Mitsubishi Gas Chemical Company, Inc.	Process for production of quaternary ammonium hydroxides
US5214182A (en) *	1987-01-12	1993-05-25	Texaco Chemical Company	Process for cogeneration of ethylene glycol and dimethyl carbonate
US4734518A (en) *	1987-01-12	1988-03-29	Texaco Inc.	Process for cosynthesis of ethylene glycol and dimethyl carbonate
US4892944A (en) *	1987-05-13	1990-01-09	Mitsubishi Petrochemical Co., Ltd.	Process for producing quaternary salts
JPH03197449A (ja)	1989-12-26	1991-08-28	Mitsui Petrochem Ind Ltd	有機第四級アンモニウム化合物の製造方法
US5091543A (en) *	1990-10-15	1992-02-25	Arco Chemical Technology, Inc.	Preparation of cyclic carbonates using alkylammonium and tertiary amine catalysts
US5438034A (en) *	1993-06-09	1995-08-01	Lonza, Inc.	Quaternary ammonium carbonate compositions and preparation thereof
JPH0753478A (ja)	1993-08-20	1995-02-28	Mitsubishi Gas Chem Co Inc	第四級アンモニウム重炭酸塩の製造方法
AU4374896A (en) *	1994-12-09	1996-06-26	Lonza Inc.	Disinfecting use of quaternary ammonium carbonates
US5833741A (en) *	1997-01-16	1998-11-10	Lonza Inc.	Waterproofing and preservative compositons for wood

2002
- 2002-02-07 UA UA2004010608A patent/UA76478C2/uk unknown
- 2002-07-02 DE DE60236286T patent/DE60236286D1/de not_active Expired - Lifetime
- 2002-07-02 MX MXPA04000353 patent/MX244518B/es active IP Right Grant
- 2002-07-02 AU AU2002316559A patent/AU2002316559B2/en not_active Ceased
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- 2002-07-05 TW TW091114946A patent/TWI242546B/zh not_active IP Right Cessation
2003
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Publication number	Publication date
RU2004104323A (ru)	2005-07-10
BR0211229B1 (pt)	2012-09-18
US20030023108A1 (en)	2003-01-30
PL367612A1 (pl)	2005-03-07
MX244518B (es)	2007-03-28
HUP0401230A2 (en)	2004-12-28
CA2453391A1 (en)	2003-01-23
CN100396660C (zh)	2008-06-25
PL205566B1 (pl)	2010-05-31
UA76478C2 (uk)	2006-08-15
AU2002316559B2 (en)	2008-04-24
NO78493A (no)	2005-01-31
JP2004521953A (ja)	2004-07-22
CN1464873A (zh)	2003-12-31
US6784307B2 (en)	2004-08-31
MXPA04000353A (es)	2005-09-08
WO2003006419A1 (en)	2003-01-23
DE60236286D1 (de)	2010-06-17
BR0211229A (pt)	2004-08-10
US20040162343A1 (en)	2004-08-19
CA2453391C (en)	2011-05-03
KR100886984B1 (ko)	2009-03-04
EP1406856A1 (en)	2004-04-14
RU2299193C2 (ru)	2007-05-20
HU230546B1 (hu)	2016-11-28
ATE466833T1 (de)	2010-05-15
ES2345141T3 (es)	2010-09-16
JP4326327B2 (ja)	2009-09-02
US6989459B2 (en)	2006-01-24
NO20040069L (no)	2004-03-05
TWI242546B (en)	2005-11-01
ZA200400698B (en)	2004-10-15
NZ530911A (en)	2005-07-29
EP1406856B1 (en)	2010-05-05
KR20040029363A (ko)	2004-04-06

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