JP2002201247A - Method for producing rigid plastic foam - Google Patents
Method for producing rigid plastic foamInfo
- Publication number
- JP2002201247A JP2002201247A JP2000401743A JP2000401743A JP2002201247A JP 2002201247 A JP2002201247 A JP 2002201247A JP 2000401743 A JP2000401743 A JP 2000401743A JP 2000401743 A JP2000401743 A JP 2000401743A JP 2002201247 A JP2002201247 A JP 2002201247A
- Authority
- JP
- Japan
- Prior art keywords
- foam
- urethane
- producing
- modified
- rigid
- 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.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 18
- 239000002984 plastic foam Substances 0.000 title 1
- 239000006260 foam Substances 0.000 claims abstract description 39
- 150000001875 compounds Chemical class 0.000 claims abstract description 23
- 229920005830 Polyurethane Foam Polymers 0.000 claims abstract description 21
- 229920000582 polyisocyanurate Polymers 0.000 claims abstract description 21
- 239000011495 polyisocyanurate Substances 0.000 claims abstract description 21
- 239000011496 polyurethane foam Substances 0.000 claims abstract description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 15
- 239000001257 hydrogen Substances 0.000 claims abstract description 15
- 239000004604 Blowing Agent Substances 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims abstract description 11
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 11
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 11
- FRCHKSNAZZFGCA-UHFFFAOYSA-N 1,1-dichloro-1-fluoroethane Chemical compound CC(F)(Cl)Cl FRCHKSNAZZFGCA-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000009835 boiling Methods 0.000 claims abstract description 9
- 238000000034 method Methods 0.000 claims abstract 2
- 239000004088 foaming agent Substances 0.000 claims description 20
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 10
- 239000003054 catalyst Substances 0.000 claims description 8
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 7
- 150000008282 halocarbons Chemical class 0.000 claims description 6
- 239000003381 stabilizer Substances 0.000 claims description 6
- 125000000524 functional group Chemical group 0.000 claims description 5
- 239000000463 material Substances 0.000 claims 1
- 229920002635 polyurethane Polymers 0.000 claims 1
- 239000004814 polyurethane Substances 0.000 claims 1
- 150000005826 halohydrocarbons Chemical class 0.000 abstract 1
- 229920005862 polyol Polymers 0.000 description 16
- 150000003077 polyols Chemical class 0.000 description 15
- 238000005187 foaming Methods 0.000 description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- -1 hydrogen compound Chemical class 0.000 description 4
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 229920000570 polyether Polymers 0.000 description 3
- 230000000630 rising effect Effects 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 description 1
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical group FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 description 1
- 102100021943 C-C motif chemokine 2 Human genes 0.000 description 1
- 102100033040 Carbonic anhydrase 12 Human genes 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 102100025989 Glyoxalase domain-containing protein 4 Human genes 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 101000897480 Homo sapiens C-C motif chemokine 2 Proteins 0.000 description 1
- 101000867855 Homo sapiens Carbonic anhydrase 12 Proteins 0.000 description 1
- 101000857136 Homo sapiens Glyoxalase domain-containing protein 4 Proteins 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 150000002483 hydrogen compounds Chemical class 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical class OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 239000012970 tertiary amine catalyst Substances 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
Landscapes
- Polyurethanes Or Polyureas (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は硬質ポリウレタンフ
ォームまたはウレタン変性硬質ポリイソシアヌレートフ
ォームを製造する方法に関するものであり、特に特定の
発泡剤を使用することを特徴とする硬質ポリウレタンフ
ォームまたはウレタン変性硬質ポリイソシアヌレートフ
ォームの製造方法に関するものである。The present invention relates to a method for producing a rigid polyurethane foam or a urethane-modified rigid polyisocyanurate foam, and more particularly to a rigid polyurethane foam or a urethane-modified rigid foam characterized by using a specific blowing agent. The present invention relates to a method for producing a polyisocyanurate foam.
【0002】[0002]
【従来の技術】イソシアネート基と反応し得る活性水素
含有官能基を2個以上有する活性水素含有化合物とポリ
イソシアネート化合物とを整泡剤、触媒と発泡剤の存在
下に反応させて硬質ポリウレタンフォームまたはウレタ
ン変性硬質ポリイソシアヌレートフォームを製造するこ
とは広く行われている。上記硬質ポリウレタンフォーム
またはウレタン変性硬質ポリイソシアヌレートフォーム
を製造するための発泡剤として様々な化合物が知られて
いるが主として1,1−ジクロロ−1−フルオロエタン
(HCFC−141b)が使用されている。また、通常
はHCFC−141bとともに水が併用される。2. Description of the Related Art A rigid polyurethane foam or a polyisocyanate compound is reacted with an active hydrogen-containing compound having two or more active hydrogen-containing functional groups capable of reacting with an isocyanate group in the presence of a foam stabilizer, a catalyst and a foaming agent. The production of urethane-modified rigid polyisocyanurate foams is widely practiced. Various compounds are known as foaming agents for producing the rigid polyurethane foam or urethane-modified rigid polyisocyanurate foam, but 1,1-dichloro-1-fluoroethane (HCFC-141b) is mainly used. . Usually, water is used together with HCFC-141b.
【0003】[0003]
【発明が解決しようとする課題】HCFC−141bを
発泡剤として用いる場合には、発泡剤の沸点が高いこと
に起因して硬質ポリウレタンフォームまたはウレタン変
性硬質ポリイソシアヌレートフォーム製造時の雰囲気温
度によっては泡化不足を起こし、正常な発泡体を得るこ
とが難しくなる。本発明は、この硬質ポリウレタンフォ
ームまたはウレタン変性硬質ポリイソシアヌレートフォ
ームの製造時における問題点を解決すべくなされたもの
であり、特定の発泡剤を用いることにより問題点を解決
したものである。When HCFC-141b is used as a foaming agent, depending on the ambient temperature at the time of producing a rigid polyurethane foam or a urethane-modified rigid polyisocyanurate foam due to the high boiling point of the foaming agent. Insufficient foaming makes it difficult to obtain a normal foam. SUMMARY OF THE INVENTION The present invention has been made to solve the problems at the time of producing this rigid polyurethane foam or urethane-modified rigid polyisocyanurate foam, and has solved the problems by using a specific foaming agent.
【0004】[0004]
【課題を解決するための手段】即ち、本願の第1発明
は、イソシアネート基と反応し得る活性水素含有官能基
を2個以上有する活性水素含有化合物とポリイソシアネ
ート化合物とを低沸点ハロゲン化炭化水素系発泡剤の存
在下に反応させて、硬質ポリウレタンフォームまたはウ
レタン変性硬質ポリイソシアヌレートフォームを製造す
る方法において、発泡剤として、R−404Aを0.1
〜18重量%とHCFC−141bを99.9〜82重
量%との混合物を用いることを特徴とする硬質ポリウレ
タンフォームまたはウレタン変性硬質ポリイソシアヌレ
ートフォームの製造方法であり、第2発明は、整泡剤、
触媒を含有する活性水素含有化合物に発泡剤を2〜50
重量%混合し、該混合物をポリイソシアネート化合物と
反応させることを特徴とする第1発明の硬質ポリウレタ
ンフォームまたはウレタン変性硬質ポリイソシアヌレー
トフォームの製造方法であり、第3発明は、発泡剤を含
有する反応液の液温を10℃以上として使用することを
特徴とする第1発明または第2発明の硬質ポリウレタン
フォームまたはウレタン変性硬質ポリイソシアヌレート
フォームの製造方法である。That is, a first invention of the present application is to provide a method for producing a low-boiling halogenated hydrocarbon comprising an active hydrogen-containing compound having two or more active hydrogen-containing functional groups capable of reacting with an isocyanate group and a polyisocyanate compound. In the method for producing a rigid polyurethane foam or a urethane-modified rigid polyisocyanurate foam by reacting in the presence of a system-based foaming agent, R-404A is used as a foaming agent in an amount of 0.1 to 0.1%.
A method for producing a rigid polyurethane foam or a urethane-modified rigid polyisocyanurate foam, which comprises using a mixture of 1818% by weight and 99.9-82% by weight of HCFC-141b. Agent,
A blowing agent is added to the active hydrogen-containing compound containing a catalyst in an amount of 2 to 50.
% By weight and reacting the mixture with a polyisocyanate compound. The method for producing a rigid polyurethane foam or a urethane-modified rigid polyisocyanurate foam according to the first invention, wherein the third invention comprises a foaming agent. A method for producing a rigid polyurethane foam or a urethane-modified rigid polyisocyanurate foam according to the first or second invention, wherein the reaction solution is used at a temperature of 10 ° C. or higher.
【0005】ここで、R−404Aは、HFC−125
/143a/134aが44/52/4の混合物であ
り、HFC−125は(CHF2 CF3 )の構造式で示
され、HFC−143aは(CH3 CF3 )の構造式で
示され、HFC−134aは(CH2 FCF3 )の構造
式で示されるヒドロフルオロカーボンであり、HCFC
−141bは(CH3 CCl2 F)の構造式で示される
ヒドロクロロフルオロカーボンである。[0005] Here, R-404A is HFC-125.
/ 143a / 134a is a mixture of 44/52/4, HFC-125 is represented by the structural formula of (CHF 2 CF 3 ), HFC-143a is represented by the structural formula of (CH 3 CF 3 ), -134a is a hydrofluorocarbon represented by the structural formula of (CH 2 FCF 3 ),
-141b is hydrochlorofluorocarbon represented by the structural formula (CH 3 CCl 2 F).
【0006】以下に本発明を詳しく説明する。HCFC
−141bを発泡剤として用いると、硬質ポリウレタン
フォームまたはウレタン変性硬質ポリイソシアヌレート
フォーム製造時の雰囲気温度が低い場合には、発泡の立
ち上がりが遅くなる傾向が見られる。これは発泡剤の沸
点が高いことに起因すると思われる。硬質ポリウレタン
フォームまたはウレタン変性硬質ポリイソシアヌレート
フォームの製造において、HCFC−141bのような
物理的発泡剤の役割は、活性水素化合物とポリイソシア
ネート化合物との重合時の反応熱によって発泡剤が気化
し、硬質プラスチックの泡化を促すことである。Hereinafter, the present invention will be described in detail. HCFC
When -141b is used as a foaming agent, the rise of foaming tends to be delayed when the ambient temperature during production of the rigid polyurethane foam or urethane-modified rigid polyisocyanurate foam is low. This is thought to be due to the high boiling point of the blowing agent. In the production of a rigid polyurethane foam or a urethane-modified rigid polyisocyanurate foam, the role of a physical foaming agent such as HCFC-141b is that the foaming agent is vaporized by heat of reaction during polymerization of an active hydrogen compound and a polyisocyanate compound, This is to promote foaming of the hard plastic.
【0007】しかし、雰囲気温度が低くなると、反応初
期において気化に必要な反応熱が発生するまでにタイム
ラグが生じ、その間に樹脂化反応が進み、正常な発泡体
を得られなくなると考えられる。本発明者らは、物理的
発泡剤としてのHCFC−141bに、低沸点ハロゲン
化炭化水素発泡剤であるR−404Aを併用して、泡化
反応を促すことが低雰囲気温度での硬質ポリウレタンフ
ォームまたはウレタン変性硬質ポリイソシアヌレートフ
ォームの製造に効果的であることを見出し、本発明に到
った。また、反応液の温度を10℃以上、好ましくは2
0℃以上とすることで低沸点ハロゲン化炭化水素の効果
が顕著に現れることも見出した。However, when the ambient temperature is lowered, a time lag occurs before the reaction heat required for vaporization is generated at the beginning of the reaction, during which the resination reaction proceeds, and it is considered that a normal foam cannot be obtained. The present inventors have found that a combination of HCFC-141b as a physical foaming agent and R-404A as a low-boiling halogenated hydrocarbon foaming agent can promote a foaming reaction. Alternatively, they have found that they are effective in producing urethane-modified rigid polyisocyanurate foams, and have reached the present invention. The temperature of the reaction solution is 10 ° C. or higher, preferably 2 ° C.
It has also been found that when the temperature is 0 ° C. or more, the effect of the low boiling halogenated hydrocarbon is remarkably exhibited.
【0008】本発明において、発泡剤の一成分として使
用する低沸点ハロゲン化炭化水素発泡剤であるR−40
4Aの混合量は0.1〜18重量%、好ましくは0.2
〜10重量%、更に好ましくは0.3〜5重量%であ
る。該混合量が0.1重量%未満であると発泡剤として
の泡化効果を発揮することができず、また18重量%を
超えると低沸点発泡剤の突沸によってフォームの発泡が
阻害される。イソシアネート基と反応し得る活性水素含
有官能基を2個以上有する活性水素含有化合物として
は、水酸基やアミノ基などの活性水素含有官能基を2個
以上有する化合物、又はその化合物の2種以上の混合物
が挙げられる。特に、2個以上の水酸基を有する化合物
やその混合物、又はそれを主成分とし、さらにポリアミ
ンなどを含む混合物が好ましい。2個以上の水酸基を有
する化合物としては、広く使用されているポリオールが
好ましい。In the present invention, R-40, a low boiling halogenated hydrocarbon blowing agent used as one component of the blowing agent, is used.
The mixing amount of 4A is 0.1 to 18% by weight, preferably 0.2 to 18% by weight.
-10% by weight, more preferably 0.3-5% by weight. If the mixing amount is less than 0.1% by weight, the foaming effect as a foaming agent cannot be exhibited, and if it exceeds 18% by weight, foaming of the foam is inhibited by bumping of the low boiling point foaming agent. Examples of the active hydrogen-containing compound having two or more active hydrogen-containing functional groups capable of reacting with an isocyanate group include a compound having two or more active hydrogen-containing functional groups such as a hydroxyl group and an amino group, or a mixture of two or more of the compounds. Is mentioned. Particularly, a compound having two or more hydroxyl groups or a mixture thereof, or a mixture containing the compound as a main component and further containing a polyamine or the like is preferable. As the compound having two or more hydroxyl groups, a polyol widely used is preferable.
【0009】ポリオールとしては、ポリエーテル系ポリ
オール、ポリエステル系ポリオール、多価アルコール、
ポリアミン、アルカノールアミンなどが挙げられ、それ
らポリオールとその他活性水素化合物との併用が好まし
い。ポリエーテル系ポリオールとしては、多価アルコー
ル、糖類、アルカノールアミン、ポリアミン、その他の
イニシエーターに環状エーテル、特にプロピレンオキサ
イド、エチレンオキサイドなどのアルキレンオキサイド
を付加して得られるポリエーテル系ポリオールが好まし
い。ポリエステル系ポリオールとしては、多価アルコー
ル−多価カルボン酸縮合系のポリオールや環状エステル
開環重合体系のポリオールなどが挙げられ、多価アルコ
ールとしてはエチレングリコール、プロピレングリコー
ル、ジエチレングリコール、ジプロピレングリコール、
グリセリン、トリメチロールプロパン、ペンタエリスリ
トール、ジエタノールアミン、トリエタノールアミンな
どが挙げられる。As the polyol, polyether polyol, polyester polyol, polyhydric alcohol,
Examples thereof include polyamines and alkanolamines, and the combination use of these polyols and other active hydrogen compounds is preferred. As the polyether polyol, a polyether polyol obtained by adding a cyclic ether, particularly an alkylene oxide such as propylene oxide or ethylene oxide, to a polyhydric alcohol, a saccharide, an alkanolamine, a polyamine, or another initiator is preferable. Examples of the polyester-based polyol include a polyhydric alcohol-polycarboxylic acid condensation-based polyol and a cyclic ester ring-opening polymerization-based polyol.Examples of the polyhydric alcohol include ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, and the like.
Glycerin, trimethylolpropane, pentaerythritol, diethanolamine, triethanolamine and the like can be mentioned.
【0010】ポリイソシアネート化合物としては、イソ
シアネート基を2個以上有する芳香族系、脂環族系およ
び脂肪族系のポリイソシアネート、それらの2種以上の
混合物、ならびにそれらを変性して得られる変性ポリイ
ソシアネートが挙げられる。具体的には、例えば、トリ
レンジイソシアネート、ジフェニルメタンジイソシアネ
ート、ポリメチレンポリフェニルイソシアネート、キシ
リレンジイソシアネート、イソホロンジイソシアネー
ト、ヘキサメチレンジイソシアネートなどのポリイソシ
アネートやそれらのプレポリマー型変性体、ヌレート変
性体、ウレア変性体などが挙げられる。Examples of the polyisocyanate compound include aromatic, alicyclic and aliphatic polyisocyanates having two or more isocyanate groups, mixtures of two or more of them, and modified poly obtained by modifying them. Isocyanates. Specifically, for example, polyisocyanates such as tolylene diisocyanate, diphenylmethane diisocyanate, polymethylene polyphenyl isocyanate, xylylene diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate, and their prepolymer-modified, nurate-modified, and urea-modified products And the like.
【0011】活性水素化合物とポリイソシアネート化合
物を反応させる際には、通常触媒の使用が必要とされ
る。触媒としては、活性水素含有基とイソシアネート基
の反応を促進させる有機スズ化合物などの金属化合物系
触媒やトリエチレンジアミンなどの3級アミン触媒が使
用される。また、カルボン酸金属塩などのイソシアネー
ト基同士を反応させる多量化触媒が目的に応じて使用さ
れる。さらに、良好な気泡を形成するための整泡剤も多
くの場合使用される。整泡剤としてはシリコーン系整泡
剤が主として挙げられる。その他、任意に使用し得る配
合剤としては、例えば充填剤、安定剤、着色剤、難燃剤
などが挙げられる。When reacting an active hydrogen compound with a polyisocyanate compound, it is usually necessary to use a catalyst. As the catalyst, a metal compound catalyst such as an organotin compound which promotes the reaction between the active hydrogen-containing group and the isocyanate group, or a tertiary amine catalyst such as triethylenediamine is used. In addition, a multimerization catalyst such as a metal carboxylate for reacting isocyanate groups with each other is used depending on the purpose. In addition, foam stabilizers to form good cells are often used. As the foam stabilizer, a silicone-based foam stabilizer is mainly exemplified. Other optional additives include, for example, fillers, stabilizers, coloring agents, and flame retardants.
【0012】これら原料を使用し、硬質ポリウレタンフ
ォーム、硬質ウレタン変性イソシアヌレートフォームが
得られる。本発明は、特にハロゲン化炭化水素系発泡剤
の使用量の多い分野である硬質ポリウレタンフォーム、
ウレタン変性硬質ポリイソシアヌレートフォームの製造
において特に有用である。以下、実施例により本発明を
更に具体的に説明するが、本発明はこれら実施例に限定
されるものではない。Using these raw materials, a rigid polyurethane foam and a rigid urethane-modified isocyanurate foam can be obtained. The present invention is a rigid polyurethane foam which is a field in which a large amount of a halogenated hydrocarbon-based blowing agent is used,
Particularly useful in the production of urethane-modified rigid polyisocyanurate foams. Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited to these examples.
【0013】[0013]
【実施例】硬質ポリウレタンフォームにおける本発明に
よる発泡剤の評価を実施例及び比較例を用いて行った。
使用したポリオールは下記の通りである。 ポリオールA:トリエタノールアミンにプロピレンオキ
サイドを反応させた水酸基価400のポリオール ポリオールB:シュークローズにプロピレンオキサイド
を反応させた水酸基価450のポリオール また、発泡状態の評価は、次の評価基準に従って行っ
た。 ○ :泡化が良く、フォームの立ち上がりが良い ○△:泡化が良く、僅かにフォームの立ち上がりが遅れ
る △ :泡化に時間がかかり、フォームの立ち上がりが遅
れる △×:泡化に時間がかかり、フォームの立ち上がりが遅
いEXAMPLES The evaluation of the blowing agent according to the invention in rigid polyurethane foams was carried out using examples and comparative examples.
The polyols used are as follows. Polyol A: Polyol having a hydroxyl value of 400 obtained by reacting propylene oxide with triethanolamine Polyol B: Polyol having a hydroxyl value of 450 obtained by reacting propylene oxide with shoe rose The evaluation of the foaming state was performed according to the following evaluation criteria. . :: Good foaming, good foam rising ○ △: Good foaming, slightly delaying foam rising △: Long foaming, slow foam rising △ ×: Long foaming time , Form rises slowly
【0014】[0014]
【実施例1】ポリオールA:50重量部とポリオール
B:50重量部の混合物に対して、シリコーン系整泡
剤:2重量部、水:1重量部、触媒としてトリエチレン
ジアミンのDPG溶液:1重量部及び発泡剤として表−
1に示す発泡剤を混合した反応液とポリメチレンポリフ
ェニルイソシアネート(通称:クルードMDI)を所定
の液温で混合し、雰囲気温度10℃で200mm×20
0mm×100mmの木製ボックスに投入し、発泡させ
て発泡体を得た。得られた結果を表−1に示す。Example 1 To a mixture of 50 parts by weight of polyol A and 50 parts by weight of polyol B, 2 parts by weight of a silicone-based foam stabilizer, 1 part by weight of water, and 1 part by weight of a DPG solution of triethylenediamine as a catalyst: 1 part by weight Table as parts and foaming agent
The reaction solution obtained by mixing the foaming agent shown in No. 1 with polymethylene polyphenyl isocyanate (commonly called Crude MDI) was mixed at a predetermined liquid temperature, and 200 mm × 20 at an ambient temperature of 10 ° C.
It was put into a 0 mm × 100 mm wooden box and foamed to obtain a foam. Table 1 shows the obtained results.
【比較例1】発泡剤を表−1に示す如くに替えた以外は
実施例1と同様にして発泡体を得た。得られた結果を表
−1に示す。Comparative Example 1 A foam was obtained in the same manner as in Example 1 except that the foaming agent was changed as shown in Table 1. Table 1 shows the obtained results.
【0015】[0015]
【表1】 [Table 1]
【0016】[0016]
【発明の効果】本発明により、雰囲気温度が低い状態に
おいても、正常な硬質ポリウレタンフォームまたはウレ
タン変性硬質ポリイソシアヌレートフォームを製造する
ことが出来た。According to the present invention, a normal rigid polyurethane foam or urethane-modified rigid polyisocyanurate foam can be produced even at a low ambient temperature.
───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4F074 AA78 BA42 BA53 CA12 CA23 CC22Y DA02 4J034 CB03 DF01 DF11 DF14 DG01 DG02 DG03 DG04 DG14 DG23 HA01 HA06 HA07 HC01 HC02 HC03 HC11 HC12 HC22 HC25 HC32 HC34 HC44 HC46 HC52 HC61 HC63 HC64 HC65 HC66 HC67 HC71 HC73 KA01 KB05 NA01 NA02 NA05 QB16 QC01 ──────────────────────────────────────────────────続 き Continued on the front page F-term (reference) 4F074 AA78 BA42 BA53 CA12 CA23 CC22Y DA02 4J034 CB03 DF01 DF11 DF14 DG01 DG02 DG03 DG04 DG14 DG23 HA01 HA06 HA07 HC01 HC02 HC03 HC11 HC12 HC22 HC25 HC32 HC34 HC61 HC63 HC52 HC34 HC66 HC67 HC71 HC73 KA01 KB05 NA01 NA02 NA05 QB16 QC01
Claims (3)
含有官能基を2個以上有する活性水素含有化合物とポリ
イソシアネート化合物とを低沸点ハロゲン化炭化水素系
発泡剤の存在下に反応させて、硬質ポリウレタンフォー
ムまたはウレタン変性硬質ポリイソシアヌレートフォー
ムを製造する方法において、発泡剤として、R−404
Aを0.1〜18重量%とHCFC−141bを99.
9〜82重量%との混合物を用いることを特徴とする硬
質ポリウレタンフォームまたはウレタン変性硬質ポリイ
ソシアヌレートフォームの製造方法。1. A hard polyurethane comprising reacting an active hydrogen-containing compound having two or more active hydrogen-containing functional groups capable of reacting with an isocyanate group with a polyisocyanate compound in the presence of a low-boiling halogenated hydrocarbon-based blowing agent. In a method for producing a foam or a urethane-modified rigid polyisocyanurate foam, R-404 is used as a blowing agent.
A of 0.1 to 18% by weight and HCFC-141b.
A process for producing a rigid polyurethane foam or a urethane-modified rigid polyisocyanurate foam, which comprises using a mixture with 9 to 82% by weight.
合物に発泡剤を2〜50重量%混合し、該混合物をポリ
イソシアネート化合物と反応させることを特徴とする請
求項1に記載の硬質ポリウレタンフォームまたはウレタ
ン変性硬質ポリイソシアヌレートフォームの製造方法。2. The hard material according to claim 1, wherein a foaming agent is mixed with an active hydrogen-containing compound containing a foam stabilizer and a catalyst in an amount of 2 to 50% by weight, and the mixture is reacted with a polyisocyanate compound. A method for producing a polyurethane foam or a urethane-modified rigid polyisocyanurate foam.
以上として使用することを特徴とする請求項1又は2に
記載の硬質ポリウレタンフォームまたはウレタン変性硬
質ポリイソシアヌレートフォームの製造方法。3. The temperature of a reaction solution containing a foaming agent is 10 ° C.
The method for producing a rigid polyurethane foam or a urethane-modified rigid polyisocyanurate foam according to claim 1 or 2, which is used as described above.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000401743A JP2002201247A (en) | 2000-12-28 | 2000-12-28 | Method for producing rigid plastic foam |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000401743A JP2002201247A (en) | 2000-12-28 | 2000-12-28 | Method for producing rigid plastic foam |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2002201247A true JP2002201247A (en) | 2002-07-19 |
Family
ID=18866134
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2000401743A Pending JP2002201247A (en) | 2000-12-28 | 2000-12-28 | Method for producing rigid plastic foam |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2002201247A (en) |
-
2000
- 2000-12-28 JP JP2000401743A patent/JP2002201247A/en active Pending
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