以甲基丙烯酸缩水甘油酯(GMA)为单体,二乙烯基苯(DVB)为交联剂,以环己醇和正十二醇为致孔剂,过氧化苯甲酰(BPO)为引发剂,直接以50 mm×4.6 mm色谱柱为模具,通过原位聚合制备聚(GMA-DVB)型整体柱.以GMA和DVB的体积比、环己醇和十二醇的体积比以及BPO占聚合物的质量分数为三因素,以分离苯和乙苯等小分子物质时的半峰宽分离度(R_(1/2))为考察指标,进行三因素三水平的正交试验,通过测定整体柱的比表面积、孔径和孔容分布对其进行表征.结果表明,制备整体柱的最优配方为 V(GMA): V(DVB)∶ V(环己醇)∶ V(正十二醇)=0.825∶0.825∶1.32∶2.03,BPO的质量分数为0.7% .应用所制备的整体柱分离苯和乙苯等小分子物质,理论塔板数达到 37 000 塔板/m,R_(1/2)值达到7.14,完全达到基线分离,分离时间小于10 min.该方法制备整体柱的重复性好,柱效较高,基本满足商品化要求.
A monolithic column of macro porous poly(glycidyl methacrylate-divinylbenzene) (poly(GMA-DVB)) has been prepared by free radical polymerization within the confines of a chromatographic stainless steel tube (50 mm×4.6 mm).For the best separation and low back pressure,orthogonal experiments were carried out with V(cyclohexanol)∶ V(dodecanol),V(GMA)∶ V(DVB) and BPO dosage as the three main factors.The characteristic feature of the column,including specific surface area,pore volume as well as pore diameter distribution,was studied by scanning electron microscopy (SEM),mercury intrusion porosimetry analysis and BET analysis.The obtained optimum preparation conditions were that the volume ratio of GMA,DVB,cyclohexanol and dodecanol was 0.825∶0.825∶1.32∶2.03 and the BPO dosage was 0.7%(mass percentage),then it was heated at 70 ℃ for 24 h.Using this monolithic column,benzene and ethylbenzene and a drug of oxiracetam can be well separated on a high performance liquid chromatographic (HPLC) system equipped with a ultraviolet (UV) detector at 254 nm.A solution of acetonitrile-water (50∶50,v/v) for the separation of benzene and ethylbenzene,and acetonitrile-water (80∶20,v/v) for the separation of oxiracetam were used as mobile phases at a flow rate of 1 mL/min.The theoretical plate number was 37 000 plates/m and the resolution of peak width at half height (R_(1/2)) was 7.14.The separation time was less than 10 min.The monolithic column prepared by this method is reproducible and has high column efficiency.It is an economical method to prepare monolithic column,which can be applied to separate small molecules.
参考文献
[1] | Svec F,Peters E C,Sykora D,et al.J High Resol Chromatogr,2000,23(1):3 |
[2] | Minakuchi H,Ishizuka N,Nakanishi K,et al.J Chromatogr A,1998,828:83 |
[3] | Peters E C,Petro M,Svec F,et al.Anal Chem,1998,70(11):2296 |
[4] | Zhu G J,Yang C,Zhang L H,et.al.Talanta,2006,70:2 |
[5] | Xie J X,Bi K S,Qian X H,et al.Chinese Journal of Chromatography (谢晶鑫,毕开顺,钱小红,等.色谱),2009,27(2):186 |
[6] | Zhang R Y,Yang G L,Xin P Y,et al.J Chromatogr A,2009,1216:2404 |
[7] | Xie S F,Svec F,Frechet J M J.J Chromatogr A,1997,775:65 |
[8] | Svec F,Frechet J M J.J Chromatogr A,1995,702:89 |
[9] | Yang X R,Yang G L,Zhu T,et al.Chinese Journal of Chromatography (杨欣茹,杨更亮,朱涛,等.色谱),2009,27(2):197 |
[10] | Amatschek K,Necina R,Hahn R,et al.J High Resol Chromatogr,2000,23(1):47 |
[11] | Ding M Y,Zheng R,Peng H.Chinese Journal of Analytical Chemistry (丁明玉,郑睿,彭虹.分析化学),2009,37(3):395 |
[12] | Wei Y M,Huang X D,Liu R X,et al.J Sep Sci,2006,29:5 |
[13] | Tian Y,Zhong C,Fu E Q,et.al.J Chromatogr A,2009,1216:1000 |
[14] | Belyakova L A,Kazdobin K A,Belyakov V N.J Colloid Interface Sci,2005,283:488 |
[15] | Yang S,Xu H X,Liu Z Z,et al.Ion Exchange and Adsorption (杨朔,徐环昕,刘坐镇,等.离子交换与吸附),2009,25(1):70 |
- 下载量()
- 访问量()
- 您的评分:
-
10%
-
20%
-
30%
-
40%
-
50%