固相微萃取目前被广泛地用来测定液态、气态,甚至固态物质的挥发组分,不同待测物的性质决定了萃取头的种类选择。采用4种常用的SPME涂层萃取头(100μmPDMS、85μmPA、65μmPDMS/DVB、50/30μm DVB/CAR/PDMS)对茶油挥发物的提取性能进行了比较研究,结果表明:65μmPDMS/DVB萃取头对较高沸点物质如苯甲醛、正辛醛、正辛醇、正壬醛、正壬醇的吸附比50/30μmDVB/CAR/PDMS萃取头要灵敏,但50/30μm DVB/CAR/PDMS萃取头对较低沸点物质的吸咐要灵敏很多。DVB/CAR/PDMS涂层萃取头所得的总峰面积的平均值最大,其余依次是PDMS/DVB、PA、PDMS;DVB/CAR/PDMS、PDMS/DVB、PA、PDMS对挥发物吸咐总峰面积与挥发物总量之间存在有线性关系,其相关系数(R2)分别是0.9939、0.9888、0.9176、0.9917;因此,65μm PDMS/DVB和50/30μm DVB/CAR/PDMS的萃取头较适用于茶油挥发物的提取。
Solid phase micro extraction (SPME) has been widely used for volatile extraction of gas, liquid and solid matrices. Four fibers, i.e. 100 μmPDMS, 85 μmPA, 65 μmPDMS/DVB and 50/30 μmDVB/CAR/PDMS, were selected for extraction in camellia oil volatile analysis. Results show that: (1) Benzaldehyde, octanal, octonol, nonanal, and nonanol which have relatively high boiling points are sensitive in 65 tan PDMS/DVB fiber, while the relatively low boiling point compounds are sensitive in 50/30 μm DVB/CAR/PDMS fiber; (2) The rank sequence of total peak areas in gas chromatography is DVB/CAR/PDMS 〉 PDMS/DVB 〉 PA 〉 PDMS; (3) Linear regressive relationship between the total peak area and volatile amount (0- 120 μg/g) in DVB/CAR/PDMS, PDMS/DVB, PA, PDMS exists with R2 of 0.9939, 0.9888, 0.9176 and 0.9917, respectively. These factors indicate that 65 μm PDMS/DVB and 50/30 tan DVB/CAR/ PDMS are suitable for the extraction of volatile of camellia oil.