功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2013年
17期
2578-2582
,共5页
蒋文俊%姚其胜%范仲勇%侯一斌%陆企亭
蔣文俊%姚其勝%範仲勇%侯一斌%陸企亭
장문준%요기성%범중용%후일빈%륙기정
偏苯三酸酐%二元醇%合成%PU 硬泡%压缩
偏苯三痠酐%二元醇%閤成%PU 硬泡%壓縮
편분삼산항%이원순%합성%PU 경포%압축
trimellitic anhydride%dihydroxy alcohol%synthesis%PU rigid foams%compressive properties
以偏苯三酸酐、乙二醇或1,3-丁二醇为原料,单丁基氧化锡为催化剂,成功合成出多官能高羟值的偏苯三酸酐-乙二醇聚酯多元醇(TEPES)、偏苯三酸酐-1,3-丁二醇聚酯多元醇(TBPES)。结果显示,TE-PES的羟值、数均官能度(fn)及重均官能度(fw)分别为400.0mg KOH/g、6.55、7.31,TBPES 的羟值、fn及fw 分别为357.2mg KOH/g、5.87、6.49,且 TB-PES的分子量分布较TEPES窄。1 H NMR 谱与 TGA分析表明,在反应过程中二元醇与偏苯三酸酐之间不仅存在单羟基的酯化反应,也存在双羟基的酯化反应;TBPES低温热稳定性比 TEPES 好,而其高温热稳定性不如后者。以聚醚多元醇 GR-835 G、TEPES、TB-PES、多亚甲基多苯基多异氰酸酯 PM-200为主要原料,制备出多种不同复配多元醇体系的60kg/m3表观密度的PU硬泡。相比单一的GR-835G体系,TEPES与GR-835G的复配体系对 PU 硬泡压缩模量的改善有利,且其改善效果要好于 TBPES 与 GR-835 G 的复配体系。同时,TEPES 的掺入会损耗一定的压缩强度,而TBPES的掺入能使压缩性能整体都有提高。
以偏苯三痠酐、乙二醇或1,3-丁二醇為原料,單丁基氧化錫為催化劑,成功閤成齣多官能高羥值的偏苯三痠酐-乙二醇聚酯多元醇(TEPES)、偏苯三痠酐-1,3-丁二醇聚酯多元醇(TBPES)。結果顯示,TE-PES的羥值、數均官能度(fn)及重均官能度(fw)分彆為400.0mg KOH/g、6.55、7.31,TBPES 的羥值、fn及fw 分彆為357.2mg KOH/g、5.87、6.49,且 TB-PES的分子量分佈較TEPES窄。1 H NMR 譜與 TGA分析錶明,在反應過程中二元醇與偏苯三痠酐之間不僅存在單羥基的酯化反應,也存在雙羥基的酯化反應;TBPES低溫熱穩定性比 TEPES 好,而其高溫熱穩定性不如後者。以聚醚多元醇 GR-835 G、TEPES、TB-PES、多亞甲基多苯基多異氰痠酯 PM-200為主要原料,製備齣多種不同複配多元醇體繫的60kg/m3錶觀密度的PU硬泡。相比單一的GR-835G體繫,TEPES與GR-835G的複配體繫對 PU 硬泡壓縮模量的改善有利,且其改善效果要好于 TBPES 與 GR-835 G 的複配體繫。同時,TEPES 的摻入會損耗一定的壓縮彊度,而TBPES的摻入能使壓縮性能整體都有提高。
이편분삼산항、을이순혹1,3-정이순위원료,단정기양화석위최화제,성공합성출다관능고간치적편분삼산항-을이순취지다원순(TEPES)、편분삼산항-1,3-정이순취지다원순(TBPES)。결과현시,TE-PES적간치、수균관능도(fn)급중균관능도(fw)분별위400.0mg KOH/g、6.55、7.31,TBPES 적간치、fn급fw 분별위357.2mg KOH/g、5.87、6.49,차 TB-PES적분자량분포교TEPES착。1 H NMR 보여 TGA분석표명,재반응과정중이원순여편분삼산항지간불부존재단간기적지화반응,야존재쌍간기적지화반응;TBPES저온열은정성비 TEPES 호,이기고온열은정성불여후자。이취미다원순 GR-835 G、TEPES、TB-PES、다아갑기다분기다이청산지 PM-200위주요원료,제비출다충불동복배다원순체계적60kg/m3표관밀도적PU경포。상비단일적GR-835G체계,TEPES여GR-835G적복배체계대 PU 경포압축모량적개선유리,차기개선효과요호우 TBPES 여 GR-835 G 적복배체계。동시,TEPES 적참입회손모일정적압축강도,이TBPES적참입능사압축성능정체도유제고。
The trimellitic anhydride-ethanediol polyester (TEPES)and the trimellitic anhydride-1 ,3-butanediol polyester (TBPES)have been synthesized with trimellitic anhydride (TMA),ethanediol (EG)or 1 ,3-butane-diol (1 ,3-BG)as raw materials,and monobutyl tin oxide as the catalyst.The results show that,the hydroxyl value,number average functionality (fn)and weight average functionality (fw)of TEPES are 400.0mg KOH/g,6.55 and 7.31,respectively.The hydroxyl value,fn and fw of TEPES are 357.2mg KOH/g,5.87 and 6.49,respectively.It can be seen that TEPES has a wider molecular weight distribution than TBPES.1 H NMR spectra and TGA curves reveal that,during the reaction there are not only a single hydroxyl reaction,but also a dihydroxy esterification reaction between dihydroxy alcohol and TMA,which further verify the GPC re-sults.In addition,the synthesized polyester polyols both have a few raw dihydroxy alcohol,which was also i-dentified by TGA.It was indicated that TBPES has a better low temperature thermal stability than TEPES, while its high temperature thermal stability was worse than TEPES.With the same apparent density 60kg/m3 , the PU rigid foams of different polyol synergistic systems,have been prepared with GR-835G,TEPES,TBPES and PM-200,as main raw materials.Comparing to the single system with GR-835G,the compressive modulus of the polyol synergistic system between TEPES and GR-835G,has a greater improvement than that of the polyol synergistic system between TBPES and GR-835G.The compressive strength of PU rigid foams will de-crease with TEPES used,however,the compressive properties can be improved using TBPES.