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利用C_(18)固相萃取膜评价有机氯污染物的亲酯性 被引量:8
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作者 于红霞 林志芬 +3 位作者 杨怡 徐铁莲 冯建芳 王连生 《膜科学与技术》 CAS CSCD 北大核心 2002年第3期35-38,共4页
采用C18 膜模拟生物体 ,探讨了化合物在膜与水相之间分配平衡的影响因素 ,测定了卤代苯类化合物的膜 /水分配系数 .结果表明 ,随着脂溶性的增加 ,化合物分配达到平衡的时间也将增加 ;C18膜 /水分配系数的大小与水相中化合物浓度的大小和... 采用C18 膜模拟生物体 ,探讨了化合物在膜与水相之间分配平衡的影响因素 ,测定了卤代苯类化合物的膜 /水分配系数 .结果表明 ,随着脂溶性的增加 ,化合物分配达到平衡的时间也将增加 ;C18膜 /水分配系数的大小与水相中化合物浓度的大小和C18膜量的多少无关 ;C18膜 /水分配系数 (KSD)与正辛醇 /水分配系数 (KOW)之间有较好的一致性 .C18膜材料的使用 ,为有机污染物脂溶性的评价提供了一个新的方法 ,并且这一方法为复合污染体系因脂溶性所引起的基本毒性量化预测创造了条件 . 展开更多
关键词 C18固相萃取膜 评价 有机氯污染物 亲酯性 生物模拟 C18膜/水分配系数 脂溶 卤代苯
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具有自萃取功能的相变CO_(2)吸收剂体系开发 被引量:1
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作者 陆诗建 刘含笑 +5 位作者 吴黎明 方梦祥 俞徐林 赵东亚 刘玲 康国俊 《中国电机工程学报》 EI CSCD 北大核心 2024年第1期203-213,I0017,共12页
二氧化碳(CO_(2))捕集工程应用的吸收剂存在再生能耗高、传质速率低、运行损耗大等问题,严重制约了CO_(2)捕集技术的大规模推广应用。为解决这些问题,该文开发适用于低分压CO_(2)捕集的相变吸收剂。该相变吸收体系以亲水性胺N-氨乙基哌... 二氧化碳(CO_(2))捕集工程应用的吸收剂存在再生能耗高、传质速率低、运行损耗大等问题,严重制约了CO_(2)捕集技术的大规模推广应用。为解决这些问题,该文开发适用于低分压CO_(2)捕集的相变吸收剂。该相变吸收体系以亲水性胺N-氨乙基哌嗪(N-aminoethyl piperazine,AEP)为主吸收体系,添加亲脂性分相剂二正丁胺(Di-n-butylamine,DPA)和活化剂(activator,ACT)。通过核磁共振波谱(nuclear magnetic resonance,NMR)和捕集CO_(2)连续测试实验研究该相变吸收剂的性能。实验结果表明,吸收负载达1.082 mol CO_(2)/mol溶液,再生温度降至98.5℃,具有优异的吸收性能和解吸性能。NMR分析表明,反应产物具有氨基甲酸盐分子结构,捕集CO_(2)连续测试实验研究与同浓度3 mol/L一乙醇胺(Monoethanolamine,MEA)溶液进行对比分析可知,相同再生能耗下,单位体积同浓度相变体系相比MEA吸收容量提高33%以上;相同再生能耗下相变体系的再生率比MEA提高15%,相同再生率下相变体系的再生能耗比MEA降低31%以上。结果表明,该相变吸收剂对于低分压CO_(2)捕集具有良好的应用前景。 展开更多
关键词 CO_(2)捕集 亲酯性 再生能耗 自萃取 相变体系
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Efficient in-situ end-functionalization of polydienes by isothiocyanate via neodymium mediated coordinative chain transfer polymerization system
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作者 ZHANG Xiu-hui DONG Jing +2 位作者 WANG Feng LIU Heng ZHANG Xue-quan 《合成橡胶工业》 CAS 2024年第4期347-347,共1页
End-functionalization of polydiene rubbers can not only improve its compatibility with inorganic fillers,but also enhance the overall mechanical properties.Nevertheless,for traditional neodymium(Nd)diene polymerizatio... End-functionalization of polydiene rubbers can not only improve its compatibility with inorganic fillers,but also enhance the overall mechanical properties.Nevertheless,for traditional neodymium(Nd)diene polymerization systems,it is highly challenging to achieve such end-functionalizations,because most of polydienyl chains are capped withη3-allyl-Nd moiety during the end of polymerization,which shows very poor reactivity with nucleophile compounds.We launched a new diene polymerization strategy calling coordinative chain transfer polymerization(CCTP)[1].In such a system,all the polydienyl chains are capped withη1-allyl-Al moieties,which reveal greater reactivity with cyclic esters and epoxide compounds,providing an effective manner to prepare polydiene-polyester amphiphilic block copolymers.Inspired by such findings,we now show herein how such types of chain-ends react with isot-hiocyanate to demonstrate an efficient in-situ manner to access end-functionalized polydienes by using CCTP. 展开更多
关键词 properties. POLYMERIZATION NEODYMIUM
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脂肪醇的T_b、-lgS_W、lgKow的QSPR研究
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作者 周莲 孙海霞 《科技通报》 北大核心 2009年第5期552-555,598,共5页
利用C-O键上碳原子电荷QC、分子所含碳原子个数N、有机结构中有机性无机性比值OI作为醇分子结构描述符,对其沸点Tb、溶解度SW及辛醇/水分配系数(Kow)进行了QSPR研究,结果令人满意。
关键词 量子化学参数 脂肪醇 OI AM1 亲酯性
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A Structure-properties Study of MDI-based Hydrophilic Polyether-polyester Polyurethane 被引量:1
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作者 权衡 顾振亚 吴穗生 《Journal of Donghua University(English Edition)》 EI CAS 2009年第4期408-412,共5页
A series of segmented polyether-polyester polyurethane with amorphous hydrophilic soft segment domains were prepared from 4,4'- diphenylmethane diisocyanate (MDI), polybutylene adipate (Glycol) 2000 (PBA2000), and... A series of segmented polyether-polyester polyurethane with amorphous hydrophilic soft segment domains were prepared from 4,4'- diphenylmethane diisocyanate (MDI), polybutylene adipate (Glycol) 2000 (PBA2000), and polyethylene glycol 1000 (PEG1000), with 1,4-butanediol (BDO) as the chain extender. Furthermore, several representative properties of the polyurethanes, such as moisture permeability, water resistance, hydrophilic property, and phase inversion temperature, were investigated. The studies show that the structure and concentration of soft segment have a remarkable effect on the main application properties of polyurethane. On the contrary, the functional properties of the polyurethane are almost not affected by its hard segment. 展开更多
关键词 hydrophilic polyurethane POLYETHER polyester structure property
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Surface patterning and modification of polyurethane biomaterials using silsesquioxane-gelatin additives for improved endothelial affinity 被引量:2
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作者 HOU LinXi PECK Yvonne +1 位作者 WANG XiaoWen WANG DongAn 《Science China Chemistry》 SCIE EI CAS 2014年第4期596-604,共9页
Polyurethanes(PUs) are well-known for their biocompatibility but their intrinsic inert property hampers cell-matrix interactions. Surface modifications are thus necessary to widen their use for biomedical applications... Polyurethanes(PUs) are well-known for their biocompatibility but their intrinsic inert property hampers cell-matrix interactions. Surface modifications are thus necessary to widen their use for biomedical applications. In this work, surface modifications of PU were achieved first by incorporating polyhedral oligomeric silsesquioxane(POSS), followed by alteration of the surface topography via the breath figures method. Subsequently, surface chemistry was also modified by immobilization of gelatin molecules through grafting, for the enhancement of the surface cytocompatibility. Scanning electron microscopy(SEM) was used to verify the formation of highly ordered microstructures while static contact angle, FTIR and XPS confirmed the successful grafting of gelatin molecules onto the surfaces. In vitro culture of human umbilical vein endothelial cells(HUVECs) revealed that endothelial cell adhesion and proliferation were significantly enhanced on the gelatin-modified surfaces, as shown by live/dead staining and WST-1 proliferation assay. The results indicated that the combination of the strategies yielded an interface that improves cell attachment and subsequent growth. This enhancement is important for the development of higher quality biomedical implants such as vascular grafts. 展开更多
关键词 BIOMATERIALS surface modification pattern POLYURETHANE SILSESQUIOXANE GELATIN endothelization
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