JP7276329B2 - 硬化性組成物、硬化性組成物セット、蓄熱材、及び物品 - Google Patents
硬化性組成物、硬化性組成物セット、蓄熱材、及び物品 Download PDFInfo
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- JP7276329B2 JP7276329B2 JP2020518950A JP2020518950A JP7276329B2 JP 7276329 B2 JP7276329 B2 JP 7276329B2 JP 2020518950 A JP2020518950 A JP 2020518950A JP 2020518950 A JP2020518950 A JP 2020518950A JP 7276329 B2 JP7276329 B2 JP 7276329B2
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- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Natural products C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
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- 125000001033 ether group Chemical group 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- HDNHWROHHSBKJG-UHFFFAOYSA-N formaldehyde;furan-2-ylmethanol Chemical compound O=C.OCC1=CC=CO1 HDNHWROHHSBKJG-UHFFFAOYSA-N 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- AFVYWKMVEGBLGD-UHFFFAOYSA-N hectane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC AFVYWKMVEGBLGD-UHFFFAOYSA-N 0.000 description 1
- FNAZRRHPUDJQCJ-UHFFFAOYSA-N henicosane Chemical compound CCCCCCCCCCCCCCCCCCCCC FNAZRRHPUDJQCJ-UHFFFAOYSA-N 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000002463 lignoceryl group Chemical group [H]C([*])([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])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])[H] 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- SOOARYARZPXNAL-UHFFFAOYSA-N methyl-thiophenol Natural products CSC1=CC=CC=C1O SOOARYARZPXNAL-UHFFFAOYSA-N 0.000 description 1
- 125000002819 montanyl group Chemical group [H]C([*])([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])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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 208000015325 multicentric Castleman disease Diseases 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([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])C([H])([H])[H] 0.000 description 1
- VAMFXQBUQXONLZ-UHFFFAOYSA-N n-alpha-eicosene Natural products CCCCCCCCCCCCCCCCCCC=C VAMFXQBUQXONLZ-UHFFFAOYSA-N 0.000 description 1
- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
- 229940094933 n-dodecane Drugs 0.000 description 1
- SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical compound ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 0.000 description 1
- KQSABULTKYLFEV-UHFFFAOYSA-N naphthalene-1,5-diamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1N KQSABULTKYLFEV-UHFFFAOYSA-N 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- PFLUOWJPZLHUEA-UHFFFAOYSA-N pentacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC PFLUOWJPZLHUEA-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
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- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 229950006800 prenderol Drugs 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 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
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 125000006839 xylylene group Chemical group 0.000 description 1
Images
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
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- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
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- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
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- Macromonomer-Based Addition Polymer (AREA)
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Description
[1] イソシアネート基を有する化合物と、蓄熱性成分を内包したカプセルと、を含有する硬化性組成物。
[2] イソシアネート基を有する化合物が、イソシアネート基を有するモノマを含む、[1]に記載の硬化性組成物。
[3] イソシアネート基を有する化合物が、イソシアネート基を有するポリマを含む、[1]又は[2]に記載の硬化性組成物。
[4] イソシアネート基を有するポリマが、下記式(1)で表される構造単位を含む、[3]に記載の硬化性組成物。
[5] イソシアネート基を有するポリマが、下記式(2)で表される構造単位を更に含む、[4]に記載の硬化性組成物。
[6] 下記式(3)で表される構造単位を含み、イソシアネート基を有さないポリマを更に含有する、[1]~[5]のいずれかに記載の硬化性組成物。
[8] ブロックイソシアネート基を有する化合物が、ブロックイソシアネート基を有するモノマを含む、[7]に記載の硬化性組成物。
[9] ブロックイソシアネート基を有する化合物が、ブロックイソシアネート基を有するポリマを含む、[7]に記載の硬化性組成物。
[10] ブロックイソシアネート基を有するポリマが、下記式(4)で表される構造単位を含む、[9]に記載の硬化性組成物。
[11] ブロックイソシアネート基を有するポリマが、下記式(2)で表される構造単位を更に含む、[10]に記載の硬化性組成物。
[12] 下記式(3)で表される構造単位を含み、ブロックイソシアネート基を有さないポリマを更に含有する、[7]~[11]のいずれかに記載の硬化性組成物。
[13] 硬化剤が、アルコール化合物、アミン化合物及びチオール化合物からなる群より選ばれる少なくとも1種である、[7]~[12]のいずれかに記載の硬化性組成物。
[14] 硬化剤がアルコール化合物である、[7]~[12]のいずれかに記載の硬化性組成物。
[15] 50℃において液体状である、[1]~[14]のいずれかに記載の硬化性組成物。
[16] 蓄熱材の形成に用いられる、[1]~[15]のいずれかに記載の硬化性組成物。
[17] [1]~[16]のいずれかに記載の硬化性組成物の硬化物を含む、蓄熱材。
[19] イソシアネート基を有する化合物が、イソシアネート基を有するモノマを含む、[18]に記載の硬化性組成物セット。
[20] イソシアネート基を有する化合物が、イソシアネート基を有するポリマを含む、[18]又は[19]に記載の硬化性組成物セット。
[21] イソシアネート基を有するポリマが、下記式(1)で表される構造単位を含む、[20]に記載の硬化性組成物セット。
[22] イソシアネート基を有するポリマが、下記式(2)で表される構造単位を更に含む、[21]に記載の硬化性組成物セット。
[23] 第一液及び第二液の少なくとも一方が、下記式(3)で表される構造単位を含み、イソシアネート基を有さないポリマを更に含有する、[18]~[22]のいずれかに記載の硬化性組成物セット。
[24] 硬化剤が、アルコール化合物、アミン化合物及びチオール化合物からなる群より選ばれる少なくとも1種である、[18]~[23]のいずれかに記載の硬化性組成物セット。
[25] 硬化剤がアルコール化合物である、[18]~[23]のいずれかに記載の硬化性組成物セット。
[26] 第一液及び第二液の両方がカプセルを含有する、[18]~[25]のいずれかに記載の硬化性組成物セット。
[27] 蓄熱材の形成に用いられる、[18]~[26]のいずれかに記載の硬化性組成物セット。
[28] [18]~[27]のいずれかに記載の硬化性組成物セットにおける、第一液及び第二液の混合物の硬化物を含む、蓄熱材。
[29] 熱源と、熱源と熱的に接触するように設けられた、[17]又は[28]に記載の蓄熱材と、を備える、物品。
・測定機器:HLC-8320GPC(製品名、東ソー(株)製)
・分析カラム:TSKgel SuperMultipore HZ-H(3本連結)(製品名、東ソー(株)製)
・ガードカラム:TSKguardcolumn SuperMP(HZ)-H(製品名、東ソー(株)製)
・溶離液:THF
・測定温度:25℃
<第1実施形態>
第1実施形態に係る硬化性組成物は、イソシアネート基を有する化合物と、蓄熱性成分を内包したカプセル(以下、「蓄熱性カプセル」ともいう。)と、を含有する。
第2実施形態に係る硬化性組成物は、ブロックイソシアネート基を有する化合物と、蓄熱性成分を内包したカプセル(蓄熱性カプセル)と、硬化剤と、を含有する。蓄熱性カプセルの態様については、第1実施形態に係る硬化性組成物に用いられる態様と同様であるため説明を省略する。
一実施形態に係る硬化性組成物セットは、上述したイソシアネート基を有する化合物を含有する第一液と、硬化剤を含有する第二液と、を備え、第一液及び第二液の少なくとも一方が、蓄熱性成分を内包したカプセル(蓄熱性カプセル)を更に含有する。イソシアネート基を有する化合物、及び蓄熱性カプセルの態様については、第1実施形態に係る硬化性組成物に用いられる態様と同様であるため説明を省略する。
以上説明した硬化性組成物の硬化物、及び硬化性組成物セットの第一液及び第二液の混合物の硬化物は、蓄熱材として好適に用いられる(蓄熱材用硬化性組成物として好適である)。すなわち、一実施形態に係る蓄熱材は、上述した硬化性組成物の硬化物を含んでいる。また、他の実施形態に係る蓄熱材は、上述した硬化性組成物セットの第一液及び第二液の混合物の硬化物を含んでいる。
次に、蓄熱材を備える物品を得る方法について、蓄熱材を設ける対象として電子部品を例に挙げて説明する。図1は、一実施形態に係る蓄熱材の形成方法(蓄熱材を備える物品の製造方法)を示す模式断面図である。本実施形態に係る形成方法(製造方法)では、まず、図1(a)に示すように、蓄熱材を設ける対象である物品として電子部品1を用意する。電子部品1は、例えば、基板(例えば回路基板)2と、基板2上に設けられた半導体チップ(熱源)3と、半導体チップ3を基板2に接続する複数の接続部(例えば半田)4とを備えている。この電子部品1では、半導体チップ3が熱源となる。複数の接続部4は、互いに離間して基板2と半導体チップ3との間に設けられている。すなわち、基板2と半導体チップ3との間には、複数の接続部4同士を隔てる隙間が存在している。
以下のとおり、公知の溶液重合方法により、実施例3~4で用いた蓄熱性(メタ)アクリルポリマA及びBを合成した。
撹拌機、温度計、窒素ガス導入管、排出管及び加熱ジャケットから構成された500mLフラスコを反応器とし、モノマとしてメトキシポリエチレングリコール#1000アクリレート93g及び2-イソシアナトエチルメタクリレート(MOI)7g、溶媒として2-プロパノール81.8gを混合し、反応器に加え、室温下(25℃)、撹拌し、1時間、窒素を流した。
その後、70℃に昇温し、昇温完了後、アゾビスイソブチロニトリル0.35gをメチルエチルケトンに溶解した溶液を反応器に添加し、反応を開始させた。その後、反応器内温度70℃で撹拌し、5時間反応させた。その後、アゾビスイソブチロニトリル0.05gをメチルエチルケトンに溶解した溶液を反応器に添加し、90℃まで昇温し、更に2時間反応させた。その後、溶媒を除去、乾燥し、蓄熱性(メタ)アクリルポリマAを得た。蓄熱性(メタ)アクリルポリマAの重量平均分子量(Mw)は、15000であった。
蓄熱性(メタ)アクリルポリマBについては、MOIをヒドロキシエチルアクリレートに変更した以外は、蓄熱性(メタ)アクリルポリマAの合成例と同様の方法で合成した。得られた蓄熱性(メタ)アクリルポリマBの重量平均分子量(Mw)は、15000であった。
(実施例1)
ヘキサメチレンジイソシアネート(HDI)40g、蓄熱性カプセルとしてBA410xxP,C37(カプセルA)(アウトラストテクノロジー社製)60g、ジラウリン酸ジブチルスズ0.2gを配合し、硬化性組成物を得た。この硬化性組成物の50℃における粘度を、E型粘度計(東機産業(株)製、PE-80L)を用いて、JIS Z 8803に基づいて測定した。結果を表1に示す。次に、硬化性組成物をポリエチレンテレフタレート(PET)フィルム上に塗布し、室温下、24時間養生した。その後、PETフィルムを除去し、厚さ100μmのフィルム状の蓄熱材を得た。
ブロックイソシアネート基を有する化合物であるMF-K60B(固形分60%、旭化成(株)製)83gと、BA410xxP,C37 50gとを混合し、溶媒を除去した。その後、ジエチレントリアミン2.0g及びジラウリン酸ジブチルスズ0.25gを更に混合し、硬化性組成物を得た。この硬化性組成物の50℃における粘度を、E型粘度計(東機産業(株)製、PE-80L)を用いて、JIS Z 8803に基づいて測定した。結果を表1に示す。
次に、硬化性組成物を10cm×10cm×1mmの型枠(SUS板)中に充填し、150℃で5分硬化させ、厚さ1mmのシート状の蓄熱材を得た。
イソシアネート基を有する化合物であるA201H(旭化成(株)製)45g、及びBA410xxP,C37 55gを混合し、第一液を得た。また、ポリオールであるGP1000(硬化剤)(三洋化成(株)製)45g、BA410xxP,C37 55g、及びジラウリン酸ジブチルスズ0.16gを混合し、第二液を得た。この第一液と第二液の25℃における粘度を、E型粘度計(東機産業(株)製、PE-80L)を用いて、JIS Z 8803に基づいて測定した。結果を表2に示す。次に、ポリエチレンテレフタレート(PET)フィルムの上に10cm×10cm×1mmの型枠(SUS板)をスペーサとして設置し、その中に第一液及び第二液をミキシングノズル(トミタエンジニアリング(株)製)を用いて混合しながら充填し、別のPETフィルムを被せ、室温下、24時間養生した。養生後、PETフィルム及び型枠を除去し厚さ1mmのシート状の蓄熱材を得た。
硬化性組成物の組成を表2に示すとおりに変更した以外は、実施例3と同様の方法で硬化性組成物の粘度測定及び蓄熱材の作製を実施した。結果を表2に示す。
実施例で作製した各蓄熱材を、示差走査熱量測定計(パーキンエルマー社製、型番DSC8500)を用いて測定し、融点と蓄熱量を算出した。具体的には、20℃/分で100℃まで昇温し、100℃で3分間保持した後、10℃/分の速度で-30℃まで降温し、次いで-30℃で3分間保持した後、10℃/分の速度で100℃まで再び昇温して熱挙動を測定した。融解ピークを蓄熱材の融点とし、面積を蓄熱量とした。結果を表1、2に示す。なお、蓄熱量が30J/g以上であれば、蓄熱量に優れているといえる。
Claims (20)
- ブロックイソシアネート基を有する化合物と、
蓄熱性成分と、該蓄熱性成分を内包した外殻とを有するカプセルと、
硬化剤と、を含有する硬化性組成物であって、
前記ブロックイソシアネート基を有する化合物が、ブロックイソシアネート基を有するモノマ及びブロックイソシアネート基を有するポリマからなる群より選択される少なくとも一種を含み、
前記ブロックイソシアネート基を有するポリマが、下記式(4)で表される構造単位を含み、
前記カプセルにおける前記外殻が、メラミン樹脂、ウレタン樹脂、又はシリカで形成されている、硬化性組成物。
[式中、R 7 は水素原子又はメチル基を表し、R 8 はブロックイソシアネート基を有する有機基を表す。] - 前記硬化剤が、アルコール化合物、アミン化合物及びチオール化合物からなる群より選ばれる少なくとも1種である、請求項4~6のいずれか一項に記載の硬化性組成物。
- 前記硬化剤がアルコール化合物である、請求項4~6のいずれか一項に記載の硬化性組成物。
- 50℃において液体状である、請求項1~8のいずれか一項に記載の硬化性組成物。
- 蓄熱材の形成に用いられる、請求項1~9のいずれか一項に記載の硬化性組成物。
- 請求項1~10のいずれか一項に記載の硬化性組成物の硬化物を含む、蓄熱材。
- イソシアネート基を有する化合物を含有する第一液と、硬化剤を含有する第二液と、を備える硬化性組成物セットであって、
前記第一液及び前記第二液の少なくとも一方が、蓄熱性成分と、該蓄熱性成分を内包した外殻とを有するカプセルを更に含有し、
前記イソシアネート基を有する化合物が、イソシアネート基を有するモノマ及びイソシアネート基を有するポリマからなる群より選択される少なくとも一種を含み、
前記イソシアネート基を有するポリマが、下記式(1)で表される構造単位を含み、
前記カプセルにおける前記外殻が、メラミン樹脂、ウレタン樹脂、又はシリカで形成されている、硬化性組成物セット。
[式中、R 1 は水素原子又はメチル基を表し、R 2 はイソシアネート基を有する有機基を表す。] - 前記硬化剤が、アルコール化合物、アミン化合物及びチオール化合物からなる群より選ばれる少なくとも1種である、請求項12~14のいずれか一項に記載の硬化性組成物セット。
- 前記硬化剤がアルコール化合物である、請求項12~14のいずれか一項に記載の硬化性組成物セット。
- 前記第一液及び前記第二液の両方が前記カプセルを含有する、請求項12~16のいずれか一項に記載の硬化性組成物セット。
- 蓄熱材の形成に用いられる、請求項12~17のいずれか一項に記載の硬化性組成物セット。
- 請求項12~18のいずれか一項に記載の硬化性組成物セットにおける、前記第一液及び前記第二液の混合物の硬化物を含む、蓄熱材。
- 熱源と、
前記熱源と熱的に接触するように設けられた、請求項11又は19に記載の蓄熱材と、を備える、物品。
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