JP5718428B2 - 低vocポリアミノアルコール - Google Patents
低vocポリアミノアルコール Download PDFInfo
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- JP5718428B2 JP5718428B2 JP2013215958A JP2013215958A JP5718428B2 JP 5718428 B2 JP5718428 B2 JP 5718428B2 JP 2013215958 A JP2013215958 A JP 2013215958A JP 2013215958 A JP2013215958 A JP 2013215958A JP 5718428 B2 JP5718428 B2 JP 5718428B2
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- JP
- Japan
- Prior art keywords
- hydrogen
- methyl
- compound
- ethyl
- alkyl
- 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.)
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title description 3
- 239000001257 hydrogen Substances 0.000 claims description 53
- 229910052739 hydrogen Inorganic materials 0.000 claims description 53
- 150000001875 compounds Chemical class 0.000 claims description 49
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 29
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 26
- 150000002431 hydrogen Chemical class 0.000 claims description 25
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 18
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 239000008199 coating composition Substances 0.000 claims description 11
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 7
- 125000002837 carbocyclic group Chemical group 0.000 claims description 7
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 30
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
- 239000000047 product Substances 0.000 description 15
- YADISKICBOYXFS-UHFFFAOYSA-N 2-ethyl-2-nitropropane-1,3-diol Chemical compound CCC(CO)(CO)[N+]([O-])=O YADISKICBOYXFS-UHFFFAOYSA-N 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- 150000002828 nitro derivatives Chemical class 0.000 description 6
- 229910000564 Raney nickel Inorganic materials 0.000 description 5
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 5
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000001588 bifunctional effect Effects 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000012043 crude product Substances 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 238000003828 vacuum filtration Methods 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- ADKLAOIGYQIIGR-UHFFFAOYSA-N 2-[[(1-hydroxy-2-methylpropan-2-yl)amino]methyl]-2-nitrobutan-1-ol Chemical compound CCC(CO)([N+]([O-])=O)CNC(C)(C)CO ADKLAOIGYQIIGR-UHFFFAOYSA-N 0.000 description 2
- OIXTUWACDYSASI-UHFFFAOYSA-N 2-[[2-[(4,4-dimethyl-1,3-oxazolidin-3-yl)methyl]-2-nitrobutyl]amino]-2-methylpropan-1-ol Chemical compound OCC(C)(C)NCC(CC)([N+]([O-])=O)CN1COCC1(C)C OIXTUWACDYSASI-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 239000007868 Raney catalyst Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000001414 amino alcohols Chemical class 0.000 description 2
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 2
- 238000010979 pH adjustment Methods 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- OPCJOXGBLDJWRM-UHFFFAOYSA-N 1,2-diamino-2-methylpropane Chemical compound CC(C)(N)CN OPCJOXGBLDJWRM-UHFFFAOYSA-N 0.000 description 1
- MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-UHFFFAOYSA-N 0.000 description 1
- SJCOAADEYQKCEY-UHFFFAOYSA-N 2-amino-2-[[(1-hydroxy-2-methylpropan-2-yl)amino]methyl]butan-1-ol Chemical compound CCC(N)(CO)CNC(C)(C)CO SJCOAADEYQKCEY-UHFFFAOYSA-N 0.000 description 1
- IOAOAKDONABGPZ-UHFFFAOYSA-N 2-amino-2-ethylpropane-1,3-diol Chemical compound CCC(N)(CO)CO IOAOAKDONABGPZ-UHFFFAOYSA-N 0.000 description 1
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
- FDYANHUVNNVRFZ-UHFFFAOYSA-N CCC(CNC(C)(C)CN(C1)COCCC1(CC)[N+]([O-])=O)(CO)[N+]([O-])=O Chemical compound CCC(CNC(C)(C)CN(C1)COCCC1(CC)[N+]([O-])=O)(CO)[N+]([O-])=O FDYANHUVNNVRFZ-UHFFFAOYSA-N 0.000 description 1
- XNHDNNDCJOGBGW-UHFFFAOYSA-N CCC(CNCC(C)(C)NCC(CC)(CO)[N+]([O-])=O)(CO)[N+]([O-])=O Chemical compound CCC(CNCC(C)(C)NCC(CC)(CO)[N+]([O-])=O)(CO)[N+]([O-])=O XNHDNNDCJOGBGW-UHFFFAOYSA-N 0.000 description 1
- 238000006683 Mannich reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- -1 nitroamino alcohol Chemical compound 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000000160 oxazolidinyl group Chemical group 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/02—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
- C07C215/14—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic the nitrogen atom of the amino group being further bound to hydrocarbon groups substituted by amino groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/40—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton with quaternised nitrogen atoms bound to carbon atoms of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
- C07C215/18—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic with hydroxy groups and at least two amino groups bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Paints Or Removers (AREA)
Description
本発明は、
(a)下記式(I)
のニトロ−ジオールと化合させて、ニトロアミノジオールを生じさせる工程;並びに、
(b)前記ニトロアミノジオールを、脂肪族ニトロ基を還元することができる還元剤と接触させる工程を含む。
他に示されない限りは、全てのパーセンテージは重量パーセンテージ(重量%)である。百万分率での濃度(ppm)は重量/体積基準で計算される。「水性」組成物は水を少なくとも30重量%、好ましくは水を少なくとも35重量%、好ましくは水を少なくとも38重量%含む組成物である。好ましくは、水性組成物は5重量%を超えて有機溶媒を含まない。他に特定されない限りは、「アルキル」基は線状もしくは分岐の配置の1〜20個の炭素原子を有するヒドロカルビル基である。アルキル基は場合によっては1以上の二重結合もしくは三重結合を有する。アルキル基上での1以上のヒドロキシもしくはアルコキシ基の置換が許容される。好ましくは、アルキル基は飽和かつ非置換である。二官能性基は2つの結合点を有する置換基であり、例えば、二官能性アルキル基の一例は、−(CH2)x−(ここで、xは2〜20であり得る)であろう。
Claims (4)
- 7未満の当初pHを有する水性コーティング組成物におけるpHを調節する方法であって、前記水性コーティング組成物に下記式(V)を有する化合物を添加することを含む方法:
- R2およびR3は独立してメチルもしくはエチルであり;R4は水素であり;R5はメチルもしくはエチルであり;R6は水素もしくは−CH2C(R5)(NH2)CH2OHである、請求項1に記載の方法。
- 前記化合物(V)の量が、前記コーティング組成物中のカルボン酸基の全重量の10重量%〜125重量%の範囲内である、請求項2に記載の方法。
- 前記水性コーティング組成物のpHを7.8〜9.5の範囲に上昇させるのに十分な量の前記式(V)の化合物が、前記水性コーティング組成物に添加される、請求項2に記載の方法。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201061427275P | 2010-12-27 | 2010-12-27 | |
US61/427,275 | 2010-12-27 |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011254495A Division JP5476358B2 (ja) | 2010-12-27 | 2011-11-22 | 低vocポリアミノアルコール |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2014040603A JP2014040603A (ja) | 2014-03-06 |
JP5718428B2 true JP5718428B2 (ja) | 2015-05-13 |
Family
ID=45093446
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011254495A Active JP5476358B2 (ja) | 2010-12-27 | 2011-11-22 | 低vocポリアミノアルコール |
JP2013215958A Active JP5718428B2 (ja) | 2010-12-27 | 2013-10-17 | 低vocポリアミノアルコール |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011254495A Active JP5476358B2 (ja) | 2010-12-27 | 2011-11-22 | 低vocポリアミノアルコール |
Country Status (6)
Country | Link |
---|---|
US (2) | US8575396B2 (ja) |
EP (1) | EP2468714B1 (ja) |
JP (2) | JP5476358B2 (ja) |
CN (1) | CN102584604B (ja) |
BR (1) | BRPI1106566B1 (ja) |
CA (1) | CA2759346C (ja) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5476358B2 (ja) * | 2010-12-27 | 2014-04-23 | ダウ グローバル テクノロジーズ エルエルシー | 低vocポリアミノアルコール |
JP5551673B2 (ja) * | 2010-12-27 | 2014-07-16 | ダウ グローバル テクノロジーズ エルエルシー | 低vocポリアミン |
BR112014002100B1 (pt) | 2011-07-28 | 2021-06-22 | Dow Global Technologies Llc | Composto e tinta ou revestimento em base aquosa |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2157386A (en) * | 1937-08-19 | 1939-05-09 | Purdue Research Foundation | Hydrogenation of nitrohydroxy compounds |
US2347621A (en) * | 1941-07-12 | 1944-04-25 | Commercial Solvents Corp | Process for reduction of nitro hydroxy compounds |
US2393825A (en) | 1942-08-24 | 1946-01-29 | Commercial Solvents Corp | Polyamines |
US2413153A (en) * | 1943-03-26 | 1946-12-24 | Commercial Solvents Corp | Process for catalytic hydrogenation of aliphatic nitrohydroxy compounds |
US2381408A (en) * | 1943-04-12 | 1945-08-07 | Commerical Solvents Corp | Nitro amines and process for preparing same |
US2421165A (en) * | 1943-04-12 | 1947-05-27 | Commercial Solvents Corp | Process for preparing nitro amines |
US2587572A (en) * | 1949-04-27 | 1952-02-26 | Commercial Solvents Corp | Process for production of amino hydroxy compounds by hydrogenation of nitro hydroxy compounds |
US2673880A (en) * | 1951-08-07 | 1954-03-30 | Commercial Solvents Corp | Production of amino hydroxy compounds |
US2743241A (en) * | 1952-11-17 | 1956-04-24 | Petrolite Corp | Process for breaking petroleum emulsions |
US2828276A (en) * | 1953-02-24 | 1958-03-25 | Petrolite Corp | Certain polyepoxide treated amine modified thermoplastic phenol-aldehyde resins and method of making same |
US3054748A (en) * | 1960-05-23 | 1962-09-18 | Commercial Solvents Corp | Process for the control of bacteria in water flooding operations in secondary oil recovery |
NL269587A (ja) * | 1960-09-28 | |||
US4410746A (en) * | 1982-06-04 | 1983-10-18 | Angus Chemical Company | Preparation of nitro-olefins |
JPS61231044A (ja) * | 1985-04-05 | 1986-10-15 | Daikin Ind Ltd | 水性デイスパ−ジヨンおよびその製法 |
JPH01211749A (ja) * | 1988-02-19 | 1989-08-24 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料の処理方法 |
CA1332029C (en) * | 1988-01-21 | 1994-09-20 | Kazuto Andoh | Method for processing a silver halide color photographic material |
JPH01211750A (ja) * | 1988-02-19 | 1989-08-24 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料の処理方法 |
JPH01214846A (ja) * | 1988-02-23 | 1989-08-29 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料の処理方法 |
US5336784A (en) | 1993-06-07 | 1994-08-09 | The Regents Of The University Of California | Synthesis of 1,3,3-trinitroazetidine |
JP5051604B2 (ja) * | 2001-08-23 | 2012-10-17 | シヤチハタ株式会社 | シール |
DE602004020665D1 (de) | 2003-12-09 | 2009-05-28 | Alcon Inc | Verwendung von bisaminen zur verstärkung der antimn |
WO2008088632A2 (en) * | 2007-01-12 | 2008-07-24 | Angus Chemical Company | Aminoalcohol and biocide compositions for aqueous based systems |
BRPI1007083B1 (pt) * | 2009-04-29 | 2021-10-26 | Angus Chemical Company | Composto, e método para fazer um composto |
US8293002B2 (en) * | 2009-04-29 | 2012-10-23 | Angus Chemical Company | Tertiary aminoalcohols as low VOC additives for paints and coatings |
JP5551673B2 (ja) * | 2010-12-27 | 2014-07-16 | ダウ グローバル テクノロジーズ エルエルシー | 低vocポリアミン |
JP5476358B2 (ja) * | 2010-12-27 | 2014-04-23 | ダウ グローバル テクノロジーズ エルエルシー | 低vocポリアミノアルコール |
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2011
- 2011-11-22 JP JP2011254495A patent/JP5476358B2/ja active Active
- 2011-11-22 CA CA2759346A patent/CA2759346C/en active Active
- 2011-11-23 EP EP11190358.9A patent/EP2468714B1/en active Active
- 2011-12-12 US US13/316,716 patent/US8575396B2/en active Active
- 2011-12-21 CN CN201110452600.8A patent/CN102584604B/zh active Active
- 2011-12-26 BR BRPI1106566A patent/BRPI1106566B1/pt active IP Right Grant
-
2013
- 2013-09-25 US US14/036,560 patent/US8680338B2/en active Active
- 2013-10-17 JP JP2013215958A patent/JP5718428B2/ja active Active
Also Published As
Publication number | Publication date |
---|---|
US8680338B2 (en) | 2014-03-25 |
JP5476358B2 (ja) | 2014-04-23 |
CA2759346A1 (en) | 2012-06-27 |
US20140020601A1 (en) | 2014-01-23 |
EP2468714A1 (en) | 2012-06-27 |
CA2759346C (en) | 2014-01-28 |
US20120165521A1 (en) | 2012-06-28 |
BRPI1106566B1 (pt) | 2019-08-27 |
EP2468714B1 (en) | 2014-02-26 |
JP2012136509A (ja) | 2012-07-19 |
US8575396B2 (en) | 2013-11-05 |
BRPI1106566A2 (pt) | 2015-07-28 |
JP2014040603A (ja) | 2014-03-06 |
CN102584604B (zh) | 2014-05-14 |
CN102584604A (zh) | 2012-07-18 |
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