JP4918472B2 - 硬化性水性組成物 - Google Patents
硬化性水性組成物 Download PDFInfo
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- JP4918472B2 JP4918472B2 JP2007320595A JP2007320595A JP4918472B2 JP 4918472 B2 JP4918472 B2 JP 4918472B2 JP 2007320595 A JP2007320595 A JP 2007320595A JP 2007320595 A JP2007320595 A JP 2007320595A JP 4918472 B2 JP4918472 B2 JP 4918472B2
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- 239000000203 mixture Substances 0.000 title claims abstract description 129
- 229920001577 copolymer Polymers 0.000 claims abstract description 79
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- 150000002314 glycerols Chemical class 0.000 claims abstract description 23
- 150000001875 compounds Chemical class 0.000 claims abstract description 7
- 239000000178 monomer Substances 0.000 claims description 48
- 239000000758 substrate Substances 0.000 claims description 36
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- 150000003839 salts Chemical class 0.000 claims description 31
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 19
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 18
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 18
- 229910052698 phosphorus Inorganic materials 0.000 claims description 18
- 239000011574 phosphorus Substances 0.000 claims description 18
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- 229920005862 polyol Polymers 0.000 claims description 17
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 15
- 150000008064 anhydrides Chemical group 0.000 claims description 12
- 125000004018 acid anhydride group Chemical group 0.000 claims description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 11
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- 238000002156 mixing Methods 0.000 claims description 6
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- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 3
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- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 2
- 239000008103 glucose Substances 0.000 claims description 2
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 claims description 2
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- 229920001187 thermosetting polymer Polymers 0.000 abstract description 13
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 abstract 1
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- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 8
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 8
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- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 8
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 8
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- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 5
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 230000014759 maintenance of location Effects 0.000 description 5
- 150000004756 silanes Chemical class 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
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- 150000002148 esters Chemical class 0.000 description 4
- 239000011152 fibreglass Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000003365 glass fiber Substances 0.000 description 4
- 239000012210 heat-resistant fiber Substances 0.000 description 4
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 4
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
- 239000011976 maleic acid Substances 0.000 description 4
- 239000011572 manganese Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 3
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- 239000000654 additive Substances 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 239000010426 asphalt Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
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- 235000003891 ferrous sulphate Nutrition 0.000 description 3
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- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 3
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- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 3
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- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- NCPXQVVMIXIKTN-UHFFFAOYSA-N trisodium;phosphite Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])[O-] NCPXQVVMIXIKTN-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
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Description
のエトキシル化およびプロポキシル化グリセロールからなる群から選択される、少なくとも1種のグリセロール誘導体、を含み、
ここで、前記カルボン酸基、酸無水物基またはそれらの塩の当量数の、前記ヒドロキシル基の当量数に対する比は1/0.001から1/1までである。
CH2=C(R1)CH(R2)OR3 (I)
[式中、R1およびR2は、独立して、水素、メチルおよび−CH2OHから選択され、R3は水素、−CH2CH(CH3)OH、−CH2CH2OH、C(CH2OH)2−C2H5および(C3−C12)ポリオール残基から選択される]または式II:
ポリカルボキシ溶液(コ)ポリマーの合成
実施例1A:溶液合成ポリマー1A
すべての溶液サンプルが同じ手順で調製された。パドルスターラー、熱電対、窒素用インレットおよび還流凝縮器を備えた5リットルの丸底フラスコに1207グラムの脱イオン水の混合物を充填し、72〜74℃に加熱した。その温度で、20.6グラムの0.15%硫酸第一鉄溶液を加えた後、2分間保持した。表1に示されている配合に従ってモノマー混合物を調製した。保持後、その温度において、モノマー混合物および236グラムの脱イオン水中における16.08グラムの過硫酸ナトリウムの溶液を90分間にわたって徐々に加え、および、反応温度を72〜74℃に維持しながら、ナトリウムメタビスルフィットの溶液(214グラムの脱イオン水中において15.3グラム)を85分間にわたって徐々に加えた。この添加が完了した後、反応混合物を72℃で15分間保持した。3.06グラムの過硫酸ナトリウムのチェイス溶液(chase solution)を40グラムの脱イオン水中に溶解し、30分間にわたって徐々に加えた。その供給が完了した時、反応混合物を72〜74℃において20分間保持した。保持期間後、その反応混合物を室温にまで冷却した。45℃またはそれ以下において、スルフィットをゼロにまで低減すべく、1.0グラムの30%過酸化水素溶液をゆっくりと加えた。結果として得られた溶液ポリマーは、約47.1%の固形分含有量を有していた。
パドルスターラー、熱電対、窒素用インレットおよび還流凝縮器を備えた5リットルの丸底フラスコに535グラムの脱イオン水を充填し、92℃に加熱した。その温度で、35グラムの45%SHP溶液を加えた後、86℃にまで冷えるのを許容しながら15分間保持した。表2に示されている配合に従って、エチルアクリレートおよびアクリル酸のモノマー混合物を調製した。保持後、その温度において、温度が92℃の反応温度にまで上昇するのを許容しながら、モノマー混合物、ならびに93グラムの脱イオン水中における15グラムの過硫酸ナトリウムの溶液および33.4グラムの45%次亜燐酸ナトリウム溶液の別々の溶液を85分間にわたって徐々に加えた。この添加が完了した後、その反応混合物を92℃において20分間保持し、その後、75℃にまで冷却した。この反応混合物に0.15%硫酸第一鉄溶液の3.0グラムの溶液を加えた。10.0グラムの脱イオン水で希釈された1.3グラムの水性tert−ブチルヒドロペルオキシド(70%)の溶液および10.0グラムの脱イオン水中における0.45グラムのイソアスコルビン酸の溶液を、1分の増分におけるショット(shots)として加え、20分間保持した。このステップを繰り返した。その温度で保持した後、その反応を室温にまで冷却し、脱イオン水のブラインド希釈物(blind dilution)を40℃未満で加えた。結果として得られた溶液状のポリマーは、約46.5%の固形分含有量を有していた。
パドルスターラー、熱電対、窒素用インレットおよび還流凝縮器を備えた5リットルの丸底フラスコに1070.6グラムの脱イオン水の混合物を充填し、72〜74℃に加熱した。その温度において、14.3グラムの脱イオン水中に溶解された1.23グラムのナトリウムメタビスルフィットおよび17.1グラムの0.15%硫酸第一鉄溶液をケトルに別々に加えた後、2分間保持した。表3に示されている配合に従ってモノマー混合物を調製した。保持後、その温度において、反応温度を72〜74℃に維持しながら、モノマー混合物を120分間にわたって徐々に加え、190グラムの脱イオン水中における31.65グラムの過硫酸ナトリウムの溶液を122分間にわたって徐々に加え、および、ナトリウムメタビスルフィットの溶液(214グラムの脱イオン水中において26.8グラム)を115分間にわたって徐々に加えた。この添加が完了した後、その反応混合物を72℃で15分間保持した。3.8グラムの過硫酸ナトリウムのチェイス溶液を20.1グラムの脱イオン水中に溶解し、30分間にわたって徐々に加えた。その供給が完了した時、反応混合物を72〜74℃において20分間保持した。保持期間後、その反応混合物を室温にまで冷却した。45℃以下において、スルフィット量をゼロにまで低減すべく、1.0グラムの30%過酸化水素溶液をゆっくりと加えた。結果として得られた溶液ポリマーは、約47.1%の固形分含有量を有していた。
5リットルの丸底フラスコにパドルスターラー、熱電対、窒素用インレットおよび還流凝縮器を備え付け、そのフラスコに679.0グラムの脱イオン水および102.7グラムの45%次亜燐酸ナトリウム溶液の混合物を充填した後、92〜94℃に加熱した。以下(表4)に示されている配合によりモノマー混合物を調製した。52.9グラムの脱イオン水中に溶解された19.7グラムの過硫酸ナトリウムの溶液および52.9グラムの脱イオン水中における102.7グラムの45%次亜燐酸ナトリウム溶液の別々の溶液を同時供給物(cofeed)用に調製した。92〜94℃の反応温度を維持しながら、モノマー混合物(表4)が120分間にわたって徐々に加えられ、過硫酸ナトリウム溶液同時供給物が121分間にわたって加えられ、次亜燐酸ナトリウム溶液同時供給物が100分間にわたって加えられた。この添加が完了した後、その反応混合物を92〜94℃において15分間保持し、その後、85℃にまで冷却した。1.54グラムの過硫酸ナトリウムおよび15.4グラムの脱イオン水の溶液を調製し、ショットチェイスとして加え、20分間保持した。この保持後、その反応を室温にまで冷却した。約50.0%の最終的な固形分含有量を達成するため、必要に応じてブラインド希釈物を加えた。
水性で硬化性の熱硬化性組成物の調製
実施例1で調製された以下のポリカルボキシ(コ)ポリマーを用いて、水性で硬化性の熱硬化性組成物が調製された。
実施例1A 70AA/30EA//1.0%のSMBS(Mw:80,200; Mn:18,700)
実施例1B 70AA/30EA//1.0%のSHP(Mw:48,000; Mn:8,000)
実施例1C 100AA//1.2%のSMBS(Mw:59,000; Mn:11,000)
実施例1D 100AA//2.1%のSHP(Mw:18,100; Mn:4,500)
ポリエステルマットの処理および処理された基体の引張試験
試験方法−マットの調製:
商業的なスパンボンドニードルパンチポリエステルマット(150g/m2、未処理)を38cm×30cmのシートに切断した。シートを(重量で)10%の浴固形分におけるそれぞれの試験サンプル結合剤組成物中において浸漬コーティングし、その後、20%±1%の結合剤追加重量(基体重量のパーセンテージとしての乾燥結合剤重量)を得るべく、40psiのロール圧力を有するロールパッダーを通り抜けさせた。その後、コーティングされた基体は、通気されているか、または脱気装置を備えているMathis Oven内において、3分間、205℃で加熱することにより直ちに硬化された。
1kNのロードセルおよび−100°Fから400°Fまで(−73℃から204℃まで)の温度範囲能力を持ったジョーを収容するオーブンチャンバーを備えたInstron 4201引張試験機が、室温での引っ張り強さ(RT TS)および伸長(RT伸長)、ならびに高温での引っ張り強さ(高温TS)および幅の保持(高温での幅)の両者のために使用された。
Claims (9)
- 硬化性水性組成物であって、
(a)少なくとも2つのカルボン酸基、酸無水物基またはそれらの塩を含み、
水性組成物中で溶液である付加ポリマー、水性組成物中で溶液である付加コポリマー、およびオリゴマーから選択される、少なくとも1種のポリカルボキシポリマーまたはコポリマーであって、ポリマーの重量に基づいて30重量%以上の、カルボン酸基、酸無水物基またはそれらの塩を含むモノマーから重合された、少なくとも1種の付加コポリマーまたは付加ポリマーから成る、ポリカルボキシポリマーまたはコポリマー;
(b)1000より大きい重量平均分子量を有し、かつ少なくとも3つのヒドロキシル基を含む少なくとも1種のグリセロール誘導体であって、式I
[式中、u、v、w、x、yおよびzは相互に独立して0〜50であり、ただしu、v、w、x、yおよびzの合計がグリセロール誘導体の1000より大きい重量平均分子量を与えることを条件とする]
のエトキシル化およびプロポキシル化グリセロールからなる群から選択される、前記グリセロール誘導体:を含み、
前記カルボン酸基、酸無水物基またはそれらの塩の当量数の、前記ヒドロキシル基の当量数に対する比が1/0.001から1/1までである、硬化性水性組成物。 - 一般式 HO−(CR2−CR2−O)n−H[式中、Rは、各出現毎に独立して、HまたはC1−4アルキルであり、nは5〜100,000の間である]の少なくとも1種のポリエーテル化合物をさらに含む、請求項1記載の硬化性組成物。
- 少なくとも1種のリン含有化合物をさらに含む、請求項1記載の硬化性組成物。
- 1000以下の分子量を有する少なくとも1種の低分子量多塩基性カルボン酸をさらに含む、請求項1記載の硬化性組成物。
- 重合単位として少なくとも1種のエチレン性不飽和非イオン性アクリルモノマーを含む、少なくとも1種のエマルジョンポリマーをさらに含む、請求項1記載の硬化性組成物。
- グリセロール、エチレングリコール、ジエチレングリコール、トリエチレングリコール、ヘキサンジオール、トリメチロールプロパン、ペンタエリトリトール、ソルビトール、スクロース、グルコース、トリエタノールアミンおよびジエタノールアミンからなる群から選択される1種以上のポリオールを、全配合固形分に基づいて、0重量%から10重量%までの量でさらに含む、請求項1記載の硬化性水性組成物。
- ポリカルボキシポリマー(a)がポリアクリル酸である、請求項1記載の硬化性組成物。
- 繊維性、不織、または複合材料基体を処理する方法であって、当該方法が、
水または1以上の水性溶媒と、(a)少なくとも2つのカルボン酸基、酸無水物基またはそれらの塩を含み、水性組成物中で溶液である付加ポリマー、水性組成物中で溶液である付加コポリマー、およびオリゴマーから選択される、少なくとも1種のポリカルボキシポリマーもしくはコポリマーであって、ポリマーの重量に基づいて30重量%以上の、カルボン酸基、酸無水物基またはそれらの塩を含むモノマーから重合された、少なくとも1種の付加コポリマーまたは付加ポリマーから成る、ポリカルボキシポリマーまたはコポリマー;
(b)1000より大きい重量平均分子量を有し、かつ少なくとも3つのヒドロキシル基を含み、
式I
[式中、u、v、w、x、yおよびzは相互に独立して0〜50であり、ただしu、v、w、x、yおよびzの合計がグリセロール誘導体の1000より大きい重量平均分子量を与えることを条件とする]
のエトキシル化およびプロポキシル化グリセロールからなる群から選択される、少なくとも1種のグリセロール誘導体を混合することを含み、
ここで、前記カルボン酸基、酸無水物基またはそれらの塩の当量数の、前記ヒドロキシル基の当量数に対する比が1/0.001から1/1までである、硬化性水性組成物を形成すること;
前記基体を前記硬化性水性組成物と接触させること、または代替的に、前記硬化性水性組成物を前記基体に適用すること;並びに
前記硬化性水性組成物を100℃から400℃の温度で加熱すること:
を含む、基体を処理する方法。 - 請求項8記載の方法により製造された繊維性物品、不織物品または複合材料基体。
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US8309231B2 (en) * | 2006-05-31 | 2012-11-13 | Usg Interiors, Llc | Acoustical tile |
US7790637B2 (en) * | 2007-10-31 | 2010-09-07 | Apple Inc. | Composite laminate having an improved cosmetic surface and method of making same |
ATE490999T1 (de) * | 2007-12-19 | 2010-12-15 | Basf Se | Wässriges bindemittel für faserförmige oder körnige substrate |
FR2935707B1 (fr) * | 2008-09-11 | 2012-07-20 | Saint Gobain Isover | Composition d'encollage pour laine minerale a base de sucre hydrogene et produits isolants obtenus |
US8536259B2 (en) | 2010-06-24 | 2013-09-17 | Usg Interiors, Llc | Formaldehyde free coatings for panels |
FR2978446B1 (fr) * | 2011-07-27 | 2015-06-05 | Saint Gobain Isover | Composition d'encollage pour laine minerale a base de maltitol et produits isolants obtenus |
US9499642B2 (en) * | 2011-11-11 | 2016-11-22 | Rohm And Haas Company | Small particle size hypophosphite telomers of unsaturated carboxylic acids |
KR101898466B1 (ko) | 2011-11-11 | 2018-09-13 | 롬 앤드 하스 캄파니 | 폴리메타크릴산 무수물 텔로머 |
FR3021651A1 (fr) * | 2014-05-28 | 2015-12-04 | Saint Gobain Isover | Composition de liant pour laine minerale |
JP6418847B2 (ja) * | 2014-08-25 | 2018-11-07 | 株式会社日本触媒 | ノニオン性多価アルコール含有結合剤 |
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JP6369610B1 (ja) * | 2017-07-27 | 2018-08-08 | 富士ゼロックス株式会社 | 樹脂組成物及び樹脂成形体 |
JP7254021B2 (ja) | 2017-09-05 | 2023-04-07 | 株式会社日本触媒 | 結合剤組成物、固着体及び固着体の製造方法 |
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WO2019088991A1 (en) * | 2017-10-31 | 2019-05-09 | Basf Se | Vinyl acrylic copolymers and methods of making and use thereof |
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