JP2005534770A5 - - Google Patents
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- JP2005534770A5 JP2005534770A5 JP2004525994A JP2004525994A JP2005534770A5 JP 2005534770 A5 JP2005534770 A5 JP 2005534770A5 JP 2004525994 A JP2004525994 A JP 2004525994A JP 2004525994 A JP2004525994 A JP 2004525994A JP 2005534770 A5 JP2005534770 A5 JP 2005534770A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- tertiary amine
- bis
- mixtures
- carbamate
- 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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- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 12
- 235000013877 carbamide Nutrition 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 6
- 239000007795 chemical reaction product Substances 0.000 claims 5
- 150000003512 tertiary amines Chemical class 0.000 claims 5
- 239000004202 carbamide Substances 0.000 claims 4
- 150000001735 carboxylic acids Chemical class 0.000 claims 4
- 239000003054 catalyst Substances 0.000 claims 4
- -1 tertiary amine carbamate Chemical class 0.000 claims 4
- 229920005830 Polyurethane Foam Polymers 0.000 claims 3
- 150000001412 amines Chemical class 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 239000011496 polyurethane foam Substances 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- 229920001228 Polyisocyanate Polymers 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims 2
- 125000000524 functional group Chemical group 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 239000005056 polyisocyanate Substances 0.000 claims 2
- 229920005862 polyol Polymers 0.000 claims 2
- 150000003077 polyols Chemical class 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- NIXYMFJMHHIQAC-UHFFFAOYSA-N 1,1-bis(dimethylamino)propan-2-ol Chemical compound CC(O)C(N(C)C)N(C)C NIXYMFJMHHIQAC-UHFFFAOYSA-N 0.000 claims 1
- GXVUZYLYWKWJIM-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanamine Chemical compound NCCOCCN GXVUZYLYWKWJIM-UHFFFAOYSA-N 0.000 claims 1
- LPVCCSSTZWTHFO-UHFFFAOYSA-N 2-(dimethylamino)ethyl carbamate Chemical compound CN(C)CCOC(N)=O LPVCCSSTZWTHFO-UHFFFAOYSA-N 0.000 claims 1
- BJKRRLWNBFNWNA-UHFFFAOYSA-N 2-[2-(dimethylamino)ethoxy]ethyl carbamate Chemical compound CN(C)CCOCCOC(N)=O BJKRRLWNBFNWNA-UHFFFAOYSA-N 0.000 claims 1
- GVGWZCPKZOZRMX-UHFFFAOYSA-N 3-amino-6-(dimethylamino)-3-[3-(dimethylamino)propyl]hexan-2-ol Chemical compound CN(C)CCCC(N)(C(O)C)CCCN(C)C GVGWZCPKZOZRMX-UHFFFAOYSA-N 0.000 claims 1
- 239000004604 Blowing Agent Substances 0.000 claims 1
- 239000004971 Cross linker Substances 0.000 claims 1
- BXYVQNNEFZOBOZ-UHFFFAOYSA-N N-[3-(dimethylamino)propyl]-N',N'-dimethylpropane-1,3-diamine Chemical compound CN(C)CCCNCCCN(C)C BXYVQNNEFZOBOZ-UHFFFAOYSA-N 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive Effects 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 125000004432 carbon atoms Chemical group C* 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 150000007942 carboxylates Chemical class 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical group 0.000 claims 1
- 125000005842 heteroatoms Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 229920001296 polysiloxane Polymers 0.000 claims 1
- 239000000376 reactant Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 150000007970 thio esters Chemical class 0.000 claims 1
Claims (11)
- ポリウレタンフォームの製造方法であって、
ポリイソシアネートと、水及び有機ポリオールを含む活性水素含有成分とを、(a)ヒドロキシ及び/又はハロ官能基を有する1以上のカルボン酸と(b)1以上の三級アミン尿素との反応生成物を含む触媒有効量の遅効性アミン触媒系の存在下で反応させる段階を含んでなる方法。 - 前記反応生成物のカルボン酸が次の一般式のものである、 請求項1記載の方法。
(X)n−R−(COOH)m
式中、Rは二価以上の炭化水素基であり、Xは塩素、臭素、フッ素からなる群から選択されるハロゲン又はヒドロキシルであり、m及びnは各々独立に1以上の値を有する整数であるが、3以上のX置換基を有する炭素原子が存在しないことを条件とする。 - 前記カルボン酸の二価炭化水素基が、直鎖脂肪族炭化水素基、枝分れ脂肪族炭化水素基、脂環式炭化水素基又は芳香族炭化水素基からなる群から選択される、請求項2記載の方法。
- 前記三級アミン尿素がモノ(三級アミノアルキル)尿素、ビス(三級アミノアルキル)尿素及びこれらの混合物からなる群から選択される、請求項4記載の方法。
- 前記反応生成物が、成分(c)として、特定の反応性三級アミン、特定の三級アミンカルバミン酸塩及びこれらの混合物からなる群から選択される反応体をさらに含む、請求項1記載の方法。
- 前記特定の反応性三級アミン化合物がビス(ジメチルアミノプロピル)アミノ−2−プロパノール、ビス(ジメチルアミノプロピル)アミン、ジメチルアミノプロピルジプロパノールアミン、ビス(ジメチルアミノ)−2−プロパノール、N,N,N′−トリメチル−N′−ヒドロキシエチル−ビス(アミノエチル)エーテル及びこれらの混合物からなる群から選択される、請求項6記載の方法。
- 前記三級アミンカルバミン酸塩がジメチルアミノエトキシエチルカルバミン酸塩、ビス(ジメチルアミノプロピル)アミノ−2−プロピルカルバミン酸塩、ジメチルアミノエチルカルバミン酸塩及びこれらの混合物からなる群から選択される、請求項6記載の方法。
- 前記反応段階が、有機スズカルボン酸塩、有機スズ酸化物、有機スズチオエステル、有機スズメルカプチド及びこれらの混合物からなる群から選択される有機スズ化合物を反応させることをさらに含む、請求項1記載の方法。
- 前記反応段階が、アミン触媒、金属塩触媒、架橋剤、シリコーン界面活性剤、有機発泡剤及びこれらの混合物からなる群から選択されるポリウレタンフォーム添加剤の存在下で実施される、請求項1記載の方法。
- 有機ポリイソシアネートと、水及び有機ポリオールを含む活性水素含有成分と、(a)ヒドロキシ及び/又はハロ官能基を有する1以上のカルボン酸と(b)1以上の三級アミン尿素との反応生成物を含む触媒有効量の遅効性アミン触媒系とを含む反応で得られる繰返し単位を有するポリウレタンフォーム。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/214,448 US6818675B2 (en) | 2002-08-06 | 2002-08-06 | Process for preparing polyurethane foam |
PCT/US2003/018313 WO2004013201A1 (en) | 2002-08-06 | 2003-06-09 | Process for preparing polyurethane foam |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2005534770A JP2005534770A (ja) | 2005-11-17 |
JP2005534770A5 true JP2005534770A5 (ja) | 2006-08-03 |
JP4567449B2 JP4567449B2 (ja) | 2010-10-20 |
Family
ID=31494651
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004525994A Expired - Lifetime JP4567449B2 (ja) | 2002-08-06 | 2003-06-09 | ポリウレタンフォームの製造方法 |
Country Status (11)
Country | Link |
---|---|
US (1) | US6818675B2 (ja) |
EP (1) | EP1534766B2 (ja) |
JP (1) | JP4567449B2 (ja) |
AT (1) | ATE423153T1 (ja) |
AU (1) | AU2003243487B2 (ja) |
BR (1) | BR0313583A (ja) |
DE (1) | DE60326245D1 (ja) |
ES (1) | ES2319118T5 (ja) |
MX (1) | MXPA05001507A (ja) |
RU (1) | RU2339653C2 (ja) |
WO (1) | WO2004013201A1 (ja) |
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-
2002
- 2002-08-06 US US10/214,448 patent/US6818675B2/en not_active Expired - Lifetime
-
2003
- 2003-06-09 WO PCT/US2003/018313 patent/WO2004013201A1/en active Application Filing
- 2003-06-09 AT AT03766815T patent/ATE423153T1/de not_active IP Right Cessation
- 2003-06-09 JP JP2004525994A patent/JP4567449B2/ja not_active Expired - Lifetime
- 2003-06-09 EP EP03766815.9A patent/EP1534766B2/en not_active Expired - Lifetime
- 2003-06-09 BR BR0313583-7A patent/BR0313583A/pt not_active Application Discontinuation
- 2003-06-09 ES ES03766815.9T patent/ES2319118T5/es not_active Expired - Lifetime
- 2003-06-09 DE DE60326245T patent/DE60326245D1/de not_active Expired - Lifetime
- 2003-06-09 RU RU2005106252/04A patent/RU2339653C2/ru active
- 2003-06-09 MX MXPA05001507A patent/MXPA05001507A/es active IP Right Grant
- 2003-06-09 AU AU2003243487A patent/AU2003243487B2/en not_active Expired
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