Luo Xiao-Jun, Mai Bi-Xian, Yang Qing-Shu, Chen She-Jun, Zeng Eddy Y
State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China.
Environ Monit Assess. 2008 Oct;145(1-3):427-36. doi: 10.1007/s10661-007-0051-2. Epub 2007 Dec 13.
Water samples were collected in the Pearl River Estuary in July 2002 and April 2003. The particulate and dissolved phase polycyclic aromatic hydrocarbons (PAHs) were determined. Total PAH concentrations in water samples were higher in April of 2003 (C (p): 4.0-39.1 ng/L or 445.1-1,089.9 ng/g; C (w): 15.9-184.2 ng/L) than in July of 2002 (C (p): 2.6-26.6 ng/L or 297.7-1,336.6 ng/g; C (w): 12.9-28.3 ng/L). It was found that 5, 6-ring PAHs enrich in the inner estuary samples and so did 3-ring PAHs in the July samples. Compositional differences in the suspended particulate matter (SPM) might be responsible for this observation. The partition coefficient (K (p)) increased with the increasing of the particular organic carbon content of suspended particles as well as the salinity of water, decreased with the increase of the total suspended particles content of samples. A linear correlation between logK (OC) and logK (OW) was found in two sampling periods. The observed values of logK (OC) exceed their predicted values derived form linear free energy relationship between logK (oc) and logK (ow), which could be attributed to the nonlinear sorption of soot-like carbons in suspended particles.
2002年7月和2003年4月在珠江口采集了水样。测定了颗粒相和溶解相的多环芳烃(PAHs)。2003年4月水样中的总PAH浓度(C(p):4.0 - 39.1 ng/L或445.1 - 1,089.9 ng/g;C(w):15.9 - 184.2 ng/L)高于2002年7月(C(p):2.6 - 26.6 ng/L或297.7 - 1,336.6 ng/g;C(w):12.9 - 28.3 ng/L)。发现5、6环PAHs在河口内样品中富集,3环PAHs在7月的样品中也是如此。悬浮颗粒物(SPM)的组成差异可能是造成这种现象的原因。分配系数(K(p))随着悬浮颗粒中特定有机碳含量以及水样盐度的增加而增加,随着样品中总悬浮颗粒含量的增加而降低。在两个采样期均发现logK(OC)与logK(OW)之间存在线性相关性。logK(OC)的观测值超过了由logK(oc)与logK(ow)之间的线性自由能关系推导得到的预测值,这可能归因于悬浮颗粒中类碳黑的非线性吸附。