{"currentpage":1,"firstResult":0,"maxresult":10,"pagecode":5,"pageindex":{"endPagecode":5,"startPagecode":1},"records":[{"abstractinfo":"在转矩流变仪中用熔融接枝法制备马来酸酐(MAH)和苯乙烯(St)接枝聚丙烯(PP)—PP-g-(MAH/St)和PP-g-MAH,将其作为聚丙烯/木粉复合材料的相容剂.FTIR证实MAH和St单体与PP发生接枝反应.用SEM和DSC等手段考察两种相容剂对PP/木粉复合材料微观形貌和结晶性能的影响,探索了各种PP/木粉复合材料加工和力学性能不同的内在原因.SEM显示,PP-g-(MAH/St)改性木粉比PP-g-MAH改性木粉在PP基体中分散性更佳,木粉与PP的界面更加模糊,相容性进一步改善.DSC结果表明,PP-g-(MAH/St)改性体系可增强木粉对PP的异相成核作用,提高结晶温度和结晶度.复合材料的加工和力学性能测试结果表明,pp-g-(MAH/St)改性效果明显优于PP-g-MAH.复合材料的熔体质量流动速率随相容剂用量的增加而逐步下降,PP-g-(MAH/St)改性体系拉伸强度和弯曲强度却逐步上升,并在相容剂用量为4.8g/l00 g PP时达到极值.此时其拉伸强度达40.62 MPa,分别是未改性体系和PP-g-MAH改性体系的1.29和1.17倍;其弯曲强度达45.72 MPa,分别是未改性体系和PP-g-MAH改性体系的1.23和1.59倍;而无缺口冲击强度却在相容剂用量为3.6 g/l00 g PP时达到极值13.35 kJ/m2,分别是未改性体系和PP-g-MAH改性体系的1.62倍和1.42倍.","authors":[{"authorName":"朱德钦","id":"caae6294-5e5f-4e05-ba10-1558c2d2cb94","originalAuthorName":"朱德钦"},{"authorName":"生瑜","id":"99bf758f-88f9-484b-81ba-b3f2ee33a639","originalAuthorName":"生瑜"},{"authorName":"童庆松","id":"8b4f8772-ef93-45ad-af63-3ec9038b46fb","originalAuthorName":"童庆松"},{"authorName":"王真","id":"a2863ff2-4a8e-4ffc-b1b3-05674ced1355","originalAuthorName":"王真"}],"doi":"10.3724/SP.J.1095.2014.30629","fpage":"885","id":"bb190f41-bf85-4fa8-837a-7135b672dce3","issue":"8","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"f5a1698a-9f5e-4b24-977f-e10dcce5bfc6","keyword":"聚丙烯","originalKeyword":"聚丙烯"},{"id":"968974b5-e59c-4c65-8f73-8c889b19aa3c","keyword":"木粉","originalKeyword":"木粉"},{"id":"e047b35c-5a45-4129-b51f-e7e3301aba9d","keyword":"马来酸酐/苯乙烯单体熔融接枝聚丙烯","originalKeyword":"马来酸酐/苯乙烯双单体熔融接枝聚丙烯"},{"id":"1df2c59d-0264-491b-9e63-e78ff5f63843","keyword":"相容性","originalKeyword":"相容性"},{"id":"29b8e1bd-67aa-48e6-9d70-bfb6bc24b23a","keyword":"性能","originalKeyword":"性能"}],"language":"zh","publisherId":"yyhx201408003","title":"PP-g-(MAH/St)和PP-g-MAH对聚丙烯/木粉复合材料性能的影响","volume":"31","year":"2014"},{"abstractinfo":"用马来酸酐(MAH)、苯乙烯(St)单体固相接枝聚丙烯(PP)制备相容剂PSM,并研究了PSM在PP/Talc/TPU体系中的应用.","authors":[{"authorName":"方治齐","id":"580a3b3a-452d-47ef-8e08-32024af62e98","originalAuthorName":"方治齐"},{"authorName":"唐龙祥","id":"a71f017a-4fbb-4a35-83ad-d2df4b4ee181","originalAuthorName":"唐龙祥"},{"authorName":"刘春华","id":"94686ccc-2eee-4f13-b303-659d566a08ca","originalAuthorName":"刘春华"}],"doi":"","fpage":"83","id":"d6d599d6-751b-4c99-977b-44382ae24829","issue":"2","journal":{"abbrevTitle":"GFZCLKXYGC","coverImgSrc":"journal/img/cover/GFZCLKXYGC.jpg","id":"31","issnPpub":"1000-7555","publisherId":"GFZCLKXYGC","title":"高分子材料科学与工程"},"keywords":[{"id":"c3c1f38b-62ca-4bb0-82c0-73897b5e5155","keyword":"聚丙烯","originalKeyword":"聚丙烯"},{"id":"f0c90f9e-af09-4405-af9e-fd42ac057c1c","keyword":"马来酸酐","originalKeyword":"马来酸酐"},{"id":"e6263910-e1f2-4094-b37f-61f0f6d653ba","keyword":"固相接枝","originalKeyword":"固相接枝"}],"language":"zh","publisherId":"gfzclkxygc200302020","title":"马来酸酐苯乙烯单体固相接枝聚丙烯及其应用","volume":"19","year":"2003"},{"abstractinfo":"用双螺杆挤出机制备了聚丙烯(PP)与尼龙6(PA6)的共混物.先用多组分熔融接枝的方法将马来酸酐(MAH)和苯乙烯(St)共同接枝聚丙烯(PP)上,制得多单体接枝聚丙烯PP-g-(MAH-St),该接枝物具有较高的MAH接枝率.利用MFR、SEM、TEM和力学性能测试等分析方法,研究了多组分熔融接枝聚丙烯PP-g-(MAH-St)对PA6/PP共混物的形态结构和力学性能等的影响.结果表明,PP-g-(MAH-St)中的酸酐基团与PA6末端的氨基发生化学反应,原位形成的PP-PA6共聚物能有效地改善PA6与PP的相容性,可以使PP均匀地分散在PA6基体中,相区尺寸明显减小,可至0.1 μm.并使共混物的力学性能得到均衡的提高,冲击韧性的提高尤其显著,达到了橡胶改性所难以达到的效果.","authors":[{"authorName":"谢续明","id":"82f2d290-3848-4b8a-9c17-0e05eb9d6e88","originalAuthorName":"谢续明"},{"authorName":"李颖","id":"70737430-1df3-409b-a468-c060c6242e46","originalAuthorName":"李颖"},{"authorName":"杨讯","id":"cae4982f-a2a7-4473-a926-89117561f383","originalAuthorName":"杨讯"}],"doi":"","fpage":"141","id":"34bc7400-1547-4b21-8f73-606491dc372e","issue":"3","journal":{"abbrevTitle":"GFZCLKXYGC","coverImgSrc":"journal/img/cover/GFZCLKXYGC.jpg","id":"31","issnPpub":"1000-7555","publisherId":"GFZCLKXYGC","title":"高分子材料科学与工程"},"keywords":[{"id":"a23d17cc-cb2d-43c3-aea2-1dd75266b4a1","keyword":"尼龙6","originalKeyword":"尼龙6"},{"id":"1a4f3ab7-b012-4fbc-917c-2670257108c4","keyword":"聚丙烯","originalKeyword":"聚丙烯"},{"id":"bd3ec722-a30b-460f-947e-e3d50b1d404a","keyword":"多单体","originalKeyword":"多单体"},{"id":"bc3c35df-1aa5-404c-9d4f-e90685d69726","keyword":"反应共混","originalKeyword":"反应共混"},{"id":"1799ade7-aa4b-49f4-8d77-c45e85e44c52","keyword":"相形态","originalKeyword":"相形态"}],"language":"zh","publisherId":"gfzclkxygc200303035","title":"尼龙6/马来酸酐-苯乙烯单体接枝聚丙烯反应共混物","volume":"19","year":"2003"},{"abstractinfo":"用单螺杆挤出机研究了马来酸酐(MAH)-苯乙烯(St)多组分单体熔融接枝EVA的反应,考察了温度、引发剂用量、MAH和St用量对接枝率及凝胶率的影响.结果表明:MAH接枝率随DCP用量、St用量的增加、反应温度的降低有最大值;当EVA/MAH/St/DCP质量比为100:4:4:0.4时,MAH接枝率最大,而凝胶率最小;以St作共单体能够显著提高MAH的接枝率,抑制体系交联;St和MAH的相互作用和共聚反应生成的SMA共聚物在接枝反应中起重要作用.","authors":[{"authorName":"叶苗","id":"1c449ad3-5717-42c5-bb09-f7e9697d173d","originalAuthorName":"叶苗"},{"authorName":"谢续明","id":"abe773cf-a278-4532-8493-a23be3e50dd7","originalAuthorName":"谢续明"}],"doi":"10.3969/j.issn.1005-0299.2001.04.022","fpage":"424","id":"4bf1a675-8401-4a3a-8caf-7e9e583b1bb8","issue":"4","journal":{"abbrevTitle":"CLKXYGY","coverImgSrc":"journal/img/cover/CLKXYGY.jpg","id":"14","issnPpub":"1005-0299","publisherId":"CLKXYGY","title":"材料科学与工艺"},"keywords":[{"id":"59fa3973-9d0d-45c0-8551-803bd5f85819","keyword":"乙烯/醋酸乙烯酯共聚物","originalKeyword":"乙烯/醋酸乙烯酯共聚物"},{"id":"1b49cc24-db55-4c1a-94b9-9c084329ccdd","keyword":"马来酸酐","originalKeyword":"马来酸酐"},{"id":"40c9ee81-aad8-43ad-b09b-08eee4de2e11","keyword":"苯乙烯","originalKeyword":"苯乙烯"},{"id":"16337f53-90c9-4a6f-b01c-80859c7d74c8","keyword":"熔融接枝","originalKeyword":"熔融接枝"}],"language":"zh","publisherId":"clkxygy200104022","title":"马来酸酐-苯乙烯单体熔融接枝EVA的研究","volume":"9","year":"2001"},{"abstractinfo":"在超临界CO2介质中,颗粒状的聚丙烯马来酸酐苯乙烯通过自由基接枝聚合生成了聚丙烯-g-(马来酸酐-苯乙烯). 探讨了双组分单体的摩尔比,溶胀温度和时间,反应压力和时间等对接枝率的影响. 结果表明,苯乙烯作为一种共聚单体能够明显提高双组分的接枝率. 在50 ℃和10 MPa压力下溶胀2 h后,升温至125 ℃、17 MPa时反应4 h,双组分接枝产物的最大接枝率为10.58%,比在同样条件下聚丙烯接枝马来酸酐接枝率大1倍. 用FTIR和DSC表征了接枝共聚物的结构和热性能. 聚丙烯支链中引入苯乙烯的结构单元,使产物的Tm由158 ℃降低到154 ℃.","authors":[{"authorName":"龚亚峰","id":"7da7761d-e1e5-470c-8402-09f1b40c7f3a","originalAuthorName":"龚亚峰"},{"authorName":"张子勇","id":"36fd6c04-184e-4d20-a393-95faf885d3fb","originalAuthorName":"张子勇"},{"authorName":"张爱丰","id":"a929047a-f078-491d-8cc0-cef99ed57b39","originalAuthorName":"张爱丰"}],"doi":"10.3969/j.issn.1000-0518.2004.09.010","fpage":"914","id":"b9342189-0459-4cbe-b7b1-0cdc41cf7032","issue":"9","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"cb84c18b-791c-4781-8021-b439bc037869","keyword":"聚丙烯","originalKeyword":"聚丙烯"},{"id":"c19c192d-b056-4028-8240-f7139c47fb49","keyword":"接枝","originalKeyword":"接枝"},{"id":"964fe0cd-d617-4464-8f66-1b5ebde60026","keyword":"超临界CO2","originalKeyword":"超临界CO2"},{"id":"3b0ee9ac-6049-4659-b66d-7015a052d82b","keyword":"苯乙烯","originalKeyword":"苯乙烯"},{"id":"191eeb1d-65da-49a9-bc6d-0645fb52cf53","keyword":"马来酸酐","originalKeyword":"马来酸酐"}],"language":"zh","publisherId":"yyhx200409010","title":"聚丙烯马来酸酐苯乙烯在超临界CO2 中的双组分接枝","volume":"21","year":"2004"},{"abstractinfo":"采用熔融法进行马来酸酐(MAH)和丙烯酸丁酯(BA)单体接枝聚丙烯(PP)的研究.结果表明,在一定工艺条件下,仅添加-单体马来酸酐时,接枝率G在其加入量为4%(质量分数)时达到最大(0.65 mmol/g PP);马来酸酐添加量保持不变,接枝率随第二单体丙烯酸丁酯添加量增加而出现-极值(1.34mmol/g PP),比一单体接枝聚丙烯接枝率高出一倍,并高于文献值(0.36 mmol/gPP).经红外光谱、热失重分析和差示扫描量热分析表明,马来酸酐丙烯酸丁酯均与聚丙烯发生接枝反应,并且以短支链的形式连接在PP的主链上.","authors":[{"authorName":"张艳","id":"7ce44093-4f8b-468f-a61e-803aba0eb7b4","originalAuthorName":"张艳"},{"authorName":"程捷","id":"2c2ba5ca-6dbf-4a88-a621-b1f6e3de593e","originalAuthorName":"程捷"},{"authorName":"郭正虹","id":"d3fb9579-8060-4942-aa6a-21cfd46794c5","originalAuthorName":"郭正虹"},{"authorName":"闫红强","id":"ae9fb5ce-678a-42ea-bb42-f60fa811b32b","originalAuthorName":"闫红强"},{"authorName":"方征平","id":"a0a94e76-bffe-4ad9-9e76-87f9b8db9f44","originalAuthorName":"方征平"}],"doi":"","fpage":"4","id":"f894a433-1fa0-4c20-8620-f3e2cbf2245f","issue":"4","journal":{"abbrevTitle":"GFZCLKXYGC","coverImgSrc":"journal/img/cover/GFZCLKXYGC.jpg","id":"31","issnPpub":"1000-7555","publisherId":"GFZCLKXYGC","title":"高分子材料科学与工程"},"keywords":[{"id":"397ce1d2-958d-49ed-9122-0c669cd03409","keyword":"马来酸酐","originalKeyword":"马来酸酐"},{"id":"2fac35a0-4197-4f1d-96ab-ac3dde49f5fc","keyword":"丙烯酸丁酯","originalKeyword":"丙烯酸丁酯"},{"id":"5f5b5caf-d8b9-45da-8161-73a15ff2211f","keyword":"接枝共聚","originalKeyword":"接枝共聚"},{"id":"942370ce-3297-4ee7-b839-bf736515f18e","keyword":"聚丙烯","originalKeyword":"聚丙烯"}],"language":"zh","publisherId":"gfzclkxygc200904002","title":"马来酸酐/丙烯酸丁酯单体接枝聚丙烯","volume":"25","year":"2009"},{"abstractinfo":"用单螺杆挤出机研究了甲基丙烯酸缩水甘油酯(GMA)-苯乙烯(St)多组分单体熔融接枝微孔聚丙烯(PP)体系.研究表明,以微孔型PP做接枝基体吸收接枝单体,能够大幅度提高单体接枝率.当GMA和St的物质的量比约为16∶8时,所得接枝物的接枝率最高,而此时接枝产物的熔体流动速率最小.二者有良好的对应关系.体系中所采用的PP具有特殊的微孔结构,使得单体接枝率获得极大提高.此外还探讨了单体用量比、温度和引发剂用量等因素对反应的影响.","authors":[{"authorName":"柯华","id":"ff50ec97-3ab0-47db-a756-88edfec11950","originalAuthorName":"柯华"},{"authorName":"谢续明","id":"7e529cf3-e520-4bdf-b35d-9ac1f25bc7de","originalAuthorName":"谢续明"}],"doi":"","fpage":"216","id":"7db70e6d-e47c-448c-9554-b8168a7ed032","issue":"5","journal":{"abbrevTitle":"GFZCLKXYGC","coverImgSrc":"journal/img/cover/GFZCLKXYGC.jpg","id":"31","issnPpub":"1000-7555","publisherId":"GFZCLKXYGC","title":"高分子材料科学与工程"},"keywords":[{"id":"b5496153-e701-46a7-af99-ec642232fc17","keyword":"微孔聚丙烯","originalKeyword":"微孔聚丙烯"},{"id":"4c1f0392-cb23-4a5c-848c-a8622001ee41","keyword":"熔融接枝","originalKeyword":"熔融接枝"},{"id":"f11d2d0b-f8c7-4f0a-8cff-68a3b2291503","keyword":"苯乙烯","originalKeyword":"苯乙烯"},{"id":"014c731b-64ad-4e4f-87e6-a73f9405ea8e","keyword":"甲基丙烯酸缩水甘油酯","originalKeyword":"甲基丙烯酸缩水甘油酯"}],"language":"zh","publisherId":"gfzclkxygc200305057","title":"甲基丙烯酸缩水甘油酯-苯乙烯单体熔融接枝微孔聚丙烯","volume":"19","year":"2003"},{"abstractinfo":"改变聚丙烯(PP)熔融接枝马来酸酐(MAH)反应中的单体和引发剂的浓度以及添加适当助剂,考察了接枝产物的接枝率和在恒定剪切应力(600kPa)及温度(210℃)下的剪切粘度,验证了作者先前所提出的PP熔融接枝MAH的反应机理.即:在PP熔融接枝MAH的过程中,过氧化物自由基在熔融接枝过程中直接引发MAH单体及MAH单体聚丙烯的大分子链段发生β断裂前直接被其引发而产生的接枝反应是影响产物的接枝率和分子量的关键.在不改变单体和引发剂浓度的情况下,降低过氧化物自由基在熔融接枝过程中直接引发MAH单体反应的程度而提高聚丙烯的大分子自由基直接引发MAH单体的反应趋势,是提高接枝产物接枝率和分子量的有效途径.","authors":[{"authorName":"施德安","id":"3b49bf5a-3dac-4982-8823-f7e94e372ddc","originalAuthorName":"施德安"},{"authorName":"殷敬华","id":"24e4b83f-377f-49ea-bce5-773653b5ae7a","originalAuthorName":"殷敬华"},{"authorName":"柯卓","id":"14e2afa2-049b-4c1b-8825-9b11aca23c51","originalAuthorName":"柯卓"}],"doi":"10.3969/j.issn.1000-0518.2001.11.004","fpage":"865","id":"89a4bcc5-033d-4937-a5ce-fff84d3e27af","issue":"11","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"5cf21de4-8d92-4eab-a4e6-56c59bde3e6a","keyword":"聚丙烯","originalKeyword":"聚丙烯"},{"id":"fb7f42a6-6665-4406-be67-1a84a396c4ad","keyword":"马来酸酐","originalKeyword":"马来酸酐"},{"id":"3de3cd8a-c685-4107-bf62-ba9afdd18f4c","keyword":"熔融接枝","originalKeyword":"熔融接枝"},{"id":"f9be4269-022b-43e4-8408-fab1e2142ff9","keyword":"机理","originalKeyword":"机理"}],"language":"zh","publisherId":"yyhx200111004","title":"聚丙烯熔融接枝马来酸酐反应机理的研究","volume":"18","year":"2001"},{"abstractinfo":"采用Haake转矩流变仪制备了马来酸酐(MAH)和1-十六烯/MAH二单体熔融接枝聚丙烯(PP)体系,利用差示扫描量热仪和红外光谱分析了1-十六烯作为第二单体对MAH-g-PP接枝行为的影响.结果表明,纯MAH-g-PP体系接枝率只有0.68%,而当1-十六烯与MAH物质的量比为0.7时,接枝率达到最大值,达1.69%.接枝机理分析认为,1-十六烯作为第二单体与MAH共接枝PP时,可能与MAH发生烯反应,生成的反应物中1-十六烯部分与PP化学结构相近,使得反应物更容易接枝到PP上,从而显著提高了接枝率.","authors":[{"authorName":"雷彩红","id":"366eae09-1e5e-4b9c-8baa-b61c5d161a45","originalAuthorName":"雷彩红"},{"authorName":"李善良","id":"9075a586-978d-4952-afd0-e1c235b7db1e","originalAuthorName":"李善良"},{"authorName":"黄伟良","id":"6d66746b-c53e-4482-a209-3acf744ed206","originalAuthorName":"黄伟良"},{"authorName":"陈大华","id":"6b3b33bc-a784-4763-afb1-fed8287ac928","originalAuthorName":"陈大华"},{"authorName":"吴博","id":"32f4dc49-dc99-4081-87df-598bf4549c60","originalAuthorName":"吴博"}],"doi":"","fpage":"95","id":"091e667e-56a4-48cd-9060-98b1d4c649a0","issue":"4","journal":{"abbrevTitle":"GFZCLKXYGC","coverImgSrc":"journal/img/cover/GFZCLKXYGC.jpg","id":"31","issnPpub":"1000-7555","publisherId":"GFZCLKXYGC","title":"高分子材料科学与工程"},"keywords":[{"id":"c58570b5-5c3d-42ab-89c9-12749b00b519","keyword":"聚丙烯","originalKeyword":"聚丙烯"},{"id":"530b7262-8e7f-44df-a56d-cdd2292afe4d","keyword":"马来酸酐","originalKeyword":"马来酸酐"},{"id":"a4af60e0-34e9-4f9e-bde3-146b1fdb9e81","keyword":"1-十六烯","originalKeyword":"1-十六烯"},{"id":"c6ee38a3-a8e2-496f-acba-5591c82815ba","keyword":"熔融接枝","originalKeyword":"熔融接枝"}],"language":"zh","publisherId":"gfzclkxygc201104026","title":"1-十六烯对马来酸酐熔融接枝聚丙烯接枝行为的影响","volume":"27","year":"2011"},{"abstractinfo":"研究了有氧条件下,以二苯甲酮(BP)为光敏引发剂,马来酸酐(MAH)/苯乙烯(St)电荷转移络合物(CTC)体系为单体体系,经紫外光照射,在聚酯(PET)薄膜表面进行的薄液相接枝反应.探讨了光敏引发剂浓度、光照时间以及苯乙烯浓度对接枝效果的影响,通过表面亲水性的测试表征了接枝效果的好坏,SEM照片从直观上表征了接枝后PET薄膜表面形貌的巨大变化,大大改善了原PET膜印刷性差的特点.此外,UV光谱图作为马来酸酐苯乙烯电荷转移络合物体系的表征,初步探讨了此单体体系接枝反应的机理.","authors":[{"authorName":"周艳飞","id":"d7dcc60f-e119-4195-ae09-95c66c4d8dd6","originalAuthorName":"周艳飞"},{"authorName":"白永平","id":"d2234584-aeef-415d-9921-3064001ee80f","originalAuthorName":"白永平"},{"authorName":"魏建功","id":"03fd2925-75ee-45d9-8c9e-4e71708d0c37","originalAuthorName":"魏建功"}],"doi":"","fpage":"34","id":"499056b6-3aa4-43dd-b7a8-6e572915a24b","issue":"3","journal":{"abbrevTitle":"GFZCLKXYGC","coverImgSrc":"journal/img/cover/GFZCLKXYGC.jpg","id":"31","issnPpub":"1000-7555","publisherId":"GFZCLKXYGC","title":"高分子材料科学与工程"},"keywords":[{"id":"b0dbe78f-b262-4205-8369-bfa3f121e4f7","keyword":"马来酸酐","originalKeyword":"马来酸酐"},{"id":"389653f3-9b6e-4a39-b2ae-c67c0f36a76e","keyword":"苯乙烯","originalKeyword":"苯乙烯"},{"id":"12ab7f90-7102-481f-81fd-f62da2b14bb5","keyword":"电荷转移络合物","originalKeyword":"电荷转移络合物"},{"id":"545d01d1-9f83-4896-bbe5-1707dc312480","keyword":"光接枝","originalKeyword":"光接枝"},{"id":"9703b441-b6fb-443c-8003-f6aa79713b84","keyword":"聚酯","originalKeyword":"聚酯"}],"language":"zh","publisherId":"gfzclkxygc200603008","title":"马来酸酐/苯乙烯电荷转移络合物体系的表面光接枝反应","volume":"22","year":"2006"}],"totalpage":2395,"totalrecord":23948}