检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:雷福厚 赵慷[1] 李小燕[1,2] 卢建芳[1,2] 关瑜婷[1]
机构地区:[1]广西民族大学化学与生态工程学院,广西南宁530006 [2]广西林产化学品开发与应用重点实验室,广西南宁530006
出 处:《精细化工》2010年第1期11-15,100,共6页Fine Chemicals
基 金:国家自然科学基金资助项目(30960306);广西自然科学基金资助项目(桂科基0639026)~~
摘 要:以脱氢枞胺为模板分子,丙烯酸为功能单体,马来松香乙二醇丙烯酸酯为交联剂,合成了脱氢枞胺分子印迹聚合物,对聚合物的结构和性能进行了表征,对分离提纯脱氢枞胺的性能进行了测定。结果表明,聚合反应的最佳条件为:0.285 g脱氢枞胺(1 mmol)、0.288 g丙烯酸(4 mmol)和4.91 g马来松香乙二醇丙烯酸酯(8 mmol);反应溶剂为氯仿(30 mL),汽油(15 mL),水(300 mL)混合溶剂;引发剂为偶氮二异丁腈(0.27 g);反应时间5 h,反应温度为70-80℃,搅拌速度为300 r/m in。最佳静态吸附条件为:以体积分数为80%的乙醇为溶剂配制脱氢枞胺溶液,质量浓度为2 g/L,分子印迹聚合物为20-40目,吸附温度70℃,振荡速度150 r/m in。脱氢枞胺分子印迹聚合物对脱氢枞胺的静态平衡吸附时间为12 h,吸附量为223 mg/g,平衡解吸时间为12 h,解吸率为95.9%。经分子印迹聚合物分离纯化后的脱氢枞胺质量分数由67.4%提高到98.3%。说明该分子印迹聚合物对脱氢枞胺的特异吸附性能良好,可以达到分离纯化脱氢枞胺的目的。In this paper,the dehydroabietylamine molecularly imprinted polymer(MIP) has been synthesized with dehydroabietylamine as a template,acrylic acid as a functional monomer and ethylene glycol maleic rosinate acrylate as a crosslinker.The structure and performance of the polymer have been investigated.Its application for the separation and purification of dehydroabietylamine has also been studied.The result showed that the optimum polymerization conditions were: the mixing molar ratio of dehydroabietylamine,acrylic acid and ethylene glycol maleic rosinate acrylate is 1∶4∶8;chloroform(30 mL),gasoline(15 mL) and distilled water(300 mL) were mixed as solvents.The amount of initiator used is 5% of the total amount of reactants.The polymerization reaction was taken at 70~80 ℃ for 5 h with the stirring speed of 300 r/min.MIP′s static adsorbance for droabietylamine was determined as 223 mg/g.The desorption ratio was 95.9%.The optimum static adsorption conditions were:2 g/L dehydroabietylamine(mass concentration) in 80% alcohol solution(volume fraction) was adsorbed by 20~40 mesh MIP at 70 ℃ with stirring at 150 r/min.The purity of dehydroabietylamine was raised from 67.4% to 98.3%(mass fraction).
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.15