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101.
Xu Zhang Huanhuan Yang Xinlei Wang Wen Song Zhaojie Cui 《Frontiers of Environmental Science & Engineering》2018,12(4):6
In this research, supercritical carbon dioxide extraction (SFE) showed better extraction effect when compared with Solid- liquid extraction (SLE), Soxhlet extraction (SE) and Ultrasonic extraction (UE), not only in the rate but also the time. The comparison among these three extraction modifiers, including acetone, ethanol and methanol demonstrated that ethanol was preferred to SFE due to its high extraction effect and low toxicology. In addition, parameter of SFE, influence of temperature and pressure were investigated, and the best extraction effect was achieved at the optima conditions, temperature of 40°C and the pressure of 35 MPa. Thus, SFE is a highly effective method for flavonols extraction, requiring minimum energy and producing non-toxic byproduct. SFE-GC system is applied for the evaluation on flavonols that plays a key role in plant resistance to heavy metal, with its content and synthetase gene expression significantly increasing in plant when threatened by heavy metal. Besides, results indicated that flavonols can improve plant resistance to oxidative stress by quenching the redundant ROS in matrix.
相似文献
102.
气相色谱-质谱联用测定母乳中合成麝香 总被引:3,自引:2,他引:1
建立了凝胶渗透色谱(GPC)柱和硅胶柱净化,气相色谱-质谱(GC/MS)测定母乳中合成麝香的分析方法.实验结果表明:GC/MS在0.01μg.ml-1到1μg.ml-1的浓度范围内对4种常见合成麝香(佳乐麝香HHCB、吐纳麝香AHTN、二甲苯麝香MX和酮麝香MK)均有良好的线性响应,4种合成麝香的基质加标回收率为76%—115%,相对标准偏差为2.8%—7.4%.利用信噪比(5/1)确定该方法的定性检测限,HHCB,AHTN,MX为5ng.g-1脂重,MK为4ng.g-1脂重,定量检测限为定性检测限的2倍.采用上述方法分析了上海母乳样品中合成麝香的浓度和分布特征,发现母乳中普遍存在这4种合成麝香,浓度分别为HHCB92±70;AHTN16±12;MX26±22;MK16±14ng.g-1脂重,与欧美国家的污染水平相比,总体含量偏低. 相似文献
103.
采用纤维膜保护的三相液相微萃取(HF-LLLME)技术,对偶氮染料在人工汗液和光辐照协同作用下降解产生致癌芳香胺的分析方法进行了研究.选用苯胺、邻甲苯胺、对氯苯胺和对硝基苯胺的汗液混合溶液进行模拟样品预处理,以正辛醇为有机萃取相,在供体相pH值为9,NaC l浓度为200.gL-1,接收相为pH=1的盐酸水溶液,萃取时... 相似文献
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Panagiotis Georgios Kanellopoulos Eleni Verouti Eirini Chrysochou Konstantinos Koukoulakis Evangelos Bakeas 《环境科学学报(英文版)》2021,33(1):222-238
PM10 samples were collected from an urban/industrial site nearby Athens, where uncontrolled burning activities occur. PAHs, monocarboxylic, dicarboxylic, hydroxycarboxylic and aromatic acids, tracers from BVOC oxidation, biomass burning tracers and bisphenol A were determined. PAH, monocarboxylic acids, biomass burning tracers and bisphenol A were increased during autumn/winter, while BSOA tracers, dicarboxylic- and hydroxycarboxylic acids during summer. Regarding aromatic acids, different sources and formation mechanisms were indicated as benzoic, phthalic and trimellitic acids were peaked during summer whereas p-toluic, isophthalic and terephthalic were more abundant during autumn/winter. The Benzo[a]pyrene-equivalent carcinogenic power, carcinogenic and mutagenic activities were calculated showing significant (p < 0.05) increases during the colder months. Palmitic, succinic and malic acids were the most abundant monocarboxylic, dicarboxylic and hydrocarboxylic acids during the entire sampling period. Isoprene oxidation was the most significant contributor to BSOA as the isoprene-SOA compounds were two times more abundant than the pinene-SOA (13.4 ± 12.3 and 6.1 ± 2.9 ng/m3, respectively). Ozone has significant impact on the formation of many studied compounds showing significant correlations with: isoprene-SOA (r = 0.77), hydrocarboxylic acids (r = 0.69), pinene-SOA (r = 0.63),dicarboxylic acids (r = 0.58), and the sum of phthalic, benzoic and trimellitic acids (r = 0.44). PCA demonstrated five factors that could explain sources including plastic enriched waste burning (30.8%), oxidation of unsaturated fatty acids (23.0%), vehicle missions and cooking (9.2%), biomass burning (7.7%) and oxidation of VOCs (5.8%). The results highlight the significant contribution of plastic waste uncontrolled burning to the overall air quality degradation. 相似文献
106.
概述GC/MS联用在我国大气有机污染监测中的应用,介绍大气中有机污染物,如多环芳烃、硝基多环芳烃、多氯二苯并二恶英、多氯二苯并呋喃、碳氢化合物、苯系物、恶臭、有机硫化合物、多组分有机污染物的测定。 相似文献
107.
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109.
Polychlorinated naphthalenes (PCNs) and non-ortho chlorinated biphenyls (non-ortho CBs) were analysed in blubber, nuchal fat, liver, muscle, kidney and brain of three male harbour porpoises (Phocoena phocoena) from the west coast of Sweden. To estimate spatial variation, PCNs and non-ortho CBs were analysed in six blubber samples collected at different anatomical sites of each animal. Highest wet weight concentrations of ΣPCNs were detected in the lipid rich tissues (blubber and nuchal fat) and liver (520–730 and 520 pg/g, respectively) and lowest in brain (22 pg/g). TetraCNs were most abundant in muscle, kidney and brain, while the hexaCNs were most abundant in the lipid rich tissues and liver. The highest lipid weight concentration recorded (11 ng/g) was for the hexaCN congeners no. 66/67 in liver. These coeluting hexaCN congeners accounted for 80–100% of total hexaCNs in all tissues examined.Concentrations of Σnon-ortho CBs were highest in lipid rich tissues (220–280 pg/g wet weight). Non-ortho CB no. 77 and 169 constituted between 62–86% and 4.9–9.3%, respectively, of total Σnon-ortho CBs. No major variation of Σnon-ortho CB concentrations was found between the six different blubber sites but higher ΣPCN concentrations (wet weight) were found dorsally at the peduncle. Toxic equivalent concentrations (TEQs) showed that non-ortho CB no. 126 was the main contributor to total TEQs in all tissues, except liver in which hexaCN congener nos. 66/67 contributed to about 50% of total TEQs. 相似文献
110.