高效液相色谱法测定多环芳烃的出峰顺序探讨

目的探讨水﹑气﹑土壤中多环芳烃检测标准(HJ 478-2009﹑HJ 647-2013、HJ 784-2016)的正确出峰时间和顺序。方法用高效液相色谱来对苊烯、芴、苊、?、苯并(a)蒽进行定性分析,并与3个标准中的出峰顺序进行比较。结果苊烯、苊、芴、苯并(a)蒽、?的出峰时间分别为6.450、7.923、8.233、17.760、18.740min,与标准HJ478-2009﹑HJ647-2013的出峰顺序存在差异。结论在使用标准HJ478-2009﹑HJ647-2013、HJ 784-2016同时测定16种多环芳烃时,多环芳烃的出峰顺序及时间应以HJ 784-2016为准。     

Polycyclic Aromatic Hydrocarbons Activate the Aryl Hydrocarbon Receptor and the Constitutive Androstane Receptor to Regulate Xenobiotic Metabolism in Human Liver Cells

Polycyclic aromatic hydrocarbons (PAHs) are environmental pollutants produced by incomplete combustion of organic matter. They induce their own metabolism by upregulating xenobiotic-metabolizing enzymes such as cytochrome P450 monooxygenase 1A1 (CYP1A1) by activating the aryl hydrocarbon receptor (AHR). However, previous studies showed that individual PAHs may also interact with the constitutive androstane receptor (CAR). Here, we studied ten PAHs, different in carcinogenicity classification, for their potential to activate AHR- and CAR-dependent luciferase reporter genes in human liver cells. The majority of investigated PAHs activated AHR, while non-carcinogenic PAHs tended to activate CAR. We further characterized gene expression, protein abundancies and activities of the AHR targets CYP1A1 and 1A2, and the CAR target CYP2B6 in human HepaRG hepatoma cells. Enzyme induction patterns strongly resembled the profiles obtained at the receptor level, with AHR-activating PAHs inducing CYP1A1/1A2 and CAR-activating PAHs inducing CYP2B6. In summary, this study provides evidence that beside well-known activation of AHR, some PAHs also activate CAR, followed by subsequent expression of respective target genes. Furthermore, we found that an increased PAH ring number is associated with AHR activation as well as the induction of DNA double-strand breaks, whereas smaller PAHs activated CAR but showed no DNA-damaging potential.     

柠檬酸复合改性对多环芳烃选择性开环铂/Beta催化剂性能的影响

通过水热处理、柠檬酸处理及其复合处理对Beta分子筛进行后改性,并以改性后的载体制得铂/Beta催化剂。采用X射线衍射（XRD）、X射线荧光光谱仪（XRF）、程序升温脱附（NH₃-TPD）、红外吡啶吸附（Py-IR）、骨架铝核磁共振技术（²⁷Al MAS NMR）及骨架硅核磁共振技术（²⁹Si MAS NMR）等表征了改性前后Beta分子筛的物化性质,并考察了改性前后铂/Beta的多环芳烃选择性开环性能。结果表明,Beta分子筛在柠檬酸处理过程中可同时发生络合脱铝与骨架补铝,实现骨架铝的再分布;Beta分子筛在水热处理过程中优先脱除稳定性相对较低的Si（2 Al）处骨架铝,产生骨架缺陷的同时生成一定比例的二次介孔结构;水热-柠檬酸复合处理影响Beta分子筛骨架补铝及骨架铝再分布的效果,水热处理后Beta分子筛中存在更多的骨架缺陷,促进活性Al（OH）₂⁺物种的骨架补铝作用。当Beta分子筛采用水热-柠檬酸复合处理顺序时,骨架补铝及骨架铝再分布效果显著,样品以中强酸为主,且具有较高的B酸量与L酸量的比值,所制备催化剂的多环芳烃选择性开环活性及稳定性最优。     

气相色谱-质谱联用法测定金属皂中的多环芳烃

建立了金属皂中16种美国环保局(EPA)优先监控的多环芳烃的气相色谱-质谱(GC/MS)联用测定方法,样品先用二甲基亚砜萃取,再用环己烷进行反萃取,经硅胶柱净化后,用GC/MS分离测定。优化了16种多环芳烃(PAHs)的分离测定条件,结果16种PAHs的平均回收率为75.32%￣98.72%,精密度实验相对标准偏差(RSD)为2.19%￣6.93%,检测限(S/N=5)为0.002￣0.010mg/kg。该方法灵敏度高、准确性好,完全可以满足金属皂中多环芳烃的检测要求。     

Bioremediation of polycyclic aromatic hydrocarbons: current knowledge and future directions

Polycyclic aromatic hydrocarbons (PAHs) are a class of organic compounds that have accumulated in the natural environment mainly as a result of anthropogenic activities such as the combustion of fossil fuels. Interest has surrounded the occurrence and distribution of PAHs for many decades due to their potentially harmful effects to human health. This concern has prompted researchers to address ways to detoxify/remove these organic compounds from the natural environment. Bioremediation is one approach that has been used to remediate contaminated land and waters, and promotes the natural attenuation of the contaminants using the in situ microbial community of the site. This review discusses the variety of fungi and bacteria that are capable of these transformations, describes the major aerobic and anaerobic breakdown pathways, and highlights some of the bioremediation technologies that are currently available. Copyright © 2005 Society of Chemical Industry     

近海海洋生物体中多环芳烃的GC-MS分析

建立了气相色谱–质谱–定性离子扫描法测定近海海洋生物体中10种多环芳烃的方法.探讨了扫描方式对方法检出限的影响,以及定性离子强度比的匹配度对定性结果的影响.10种多环芳烃测定方法的检出限为0.10～0.61μg/kg,方法线性关系良好,加标回收率为63.1%～98.1%,相对标准偏差为3.9%～15.2%.此方法适用于海洋生物体中多环芳烃的分析.     

应用Markov理论定量描述土壤剖面中菲的垂向运移分布特征

马尔可夫(Markov)链理论是用来描述随时间(空间)变化的一个离散状态序列的状态转移特性的,本文将其引入来研究土壤剖面多环芳烃有机污染物的垂向变化规律,建立了基于空间离散化的马尔可夫(Markov)链理论数学模型及垂向归趋极限.研究结果表明,基于空间离散化的马尔可夫(Markov)链理论数学模型及垂向归趋极限能够很好地模拟区域土壤剖面多环芳烃(菲)的垂向变化特征,并有迁移规律的识别功能.     

介孔碳对气相多环芳烃的吸附研究

选取两种典型多环芳烃(Polycyclic Aromatic Hydrocarbons,PAHs)菲、芘为研究对象,对其在CMK-3上的吸附特性进行了研究。通过实验得到各组吸附质—吸附剂的吸附等温线及不同浓度下的穿透曲线,并分别由吸附等温线模型(Langmuir、Freundlich、DR)以及基于恒定浓度波假设的动力学模型拟合,获得相应的吸附平衡及动力学参数。研究结果表明:Langmuir模型能很好的描述低浓度的菲在CMK-3的吸附行为,Freundlich模型能很好的描述低浓度的芘在CMK-3上的吸附行为(R~299%)。基于恒定浓度波假设的穿透曲线模型能较好的预测浓度较低时PAHs的穿透曲线;相同浓度的PAHs在其上吸附的内扩散系数呈现PyrPhe的规律,而总传质系数则呈现出相反的规律,且菲的浓度越大总传质系数越大,芘正好相反。     

EPISODIC SUSPENDED SEDIMENT TRANSPORT AND ELEVATED POLYCYCLIC AROMATIC HYDROCARBON CONCENTRATIONS IN A SMALL,MOUNTAINOUS RIVER IN COASTAL CALIFORNIA

Suspended sediment and organic contaminants were measured during a period of 2 years in the San Lorenzo River, central California, which discharges into the Pacific Ocean within the Monterey Bay National Marine Sanctuary, in an effort to quantify the potential environmental effects of storm events from a steep, mountainous coastal urban watershed. Most suspended sediment transport occurred during flooding caused by winter storms; 56% of the total sediment load for the 2‐year study was transported by the river during one storm event in January 2010. Concentrations of polycyclic aromatic hydrocarbons can exceed regulatory criteria during high‐flow events in the San Lorenzo River, and total annual polycyclic aromatic hydrocarbon load was on the order of 10 kg in water year 2010. These results highlight the importance of episodic sediment and contaminant transport in steep, mountainous coastal watersheds and emphasize the importance of understanding physical processes and quantifying chemical constituents in discharge from coastal watersheds on event‐scale terms. Published 2012. This article is a U.S. Government work and is in the public domain in the USA.