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81.
Xiuying Zhao Xinming Wang Xiang Ding Quanfu He Zhou Zhang Tengyu Liu Xiaoxin Fu Bo Gao Yunpeng Wang Yanli Zhang Xuejiao Deng Dui Wu 《环境科学学报(英文版)》2014,26(1):110-121
Organic acids as important constituents of organic aerosols not only influence the aerosols' hygroscopic property, but also enhance the formation of new particles and secondary organic aerosols. This study reported organic acids including C14–C32fatty acids, C4–C9dicarboxylic acids and aromatic acids in PM2.5collected during winter 2009 at six typical urban, suburban and rural sites in the Pearl River Delta region. Averaged concentrations of C14–C32fatty acids, aromatic acids and C4– C9 dicarboxylic acids were 157, 72.5 and 50.7 ng/m3, respectively. They totally accounted for 1.7% of measured organic carbon. C20–C32fatty acids mainly deriving from higher plant wax showed the highest concentration at the upwind rural site with more vegetation around, while C14–C18fatty acids were more abundant at urban and suburban sites, and dicarboxylic acids and aromatic acids except 1,4-phthalic acid peaked at the downwind rural site. Succinic and azelaic acid were the most abundant among C4–C9dicarboxylic acids, and 1,2-phthalic and 1,4-phthalic acid were dominant aromatic acids. Dicarboxylic acids and aromatic acids exhibited significant mutual correlations except for 1,4-phthalic acid, which was probably primarily emitted from combustion of solid wastes containing polyethylene terephthalate plastics. Spatial patterns and correlations with typical source tracers suggested that C14–C32fatty acids were mainly primary while dicarboxylic and aromatic acids were largely secondary. Principal component analysis resolved six sources including biomass burning, natural higher plant wax, two mixed anthropogenic and two secondary sources; further multiple linear regression revealed their contributions to individual organic acids. It turned out that more than 70% of C14–C18fatty acids were attributed to anthropogenic sources, about 50%–85% of the C20–C32fatty acids were attributed to natural sources, 80%–95% of dicarboxylic acids and 1,2-phthalic acid were secondary in contrast with that 81% of 1,4-phthalic acid was primary. 相似文献
82.
Removal of noxious dyes is gaining public and technological attention. Herein grafting polymerization was employed to produce a novel adsorbent using acrylic acid and carboxymethyl cellulose for dye removal. Scanning electron microscopy and Fourier-transform infrared spectroscopy verified the adsorbent formed under optimized reaction conditions. The removal ratio of adsorbent to Methyl Orange, Disperse Blue 2BLN and malachite green chloride reached to 84.2%, 79.6% and 99.9%, respectively. The greater agreement between the calculated and experimental results suggested that pseudo second-order kinetic model better represents the kinetic adsorption data. Equilibrium adsorptions of dyes were better explained by the Temkin isotherm. The results implied that this new cellulose-based absorbent had the universaiity for removal of dyes through the chemical adsorption mechanism. 相似文献
83.
天津市公交站人群PM10暴露研究及PAHs健康风险评估 总被引:1,自引:0,他引:1
2012年9月在天津市城市交通密集区(八里台、海光寺公交车站)采集可吸入颗粒物(PM10)样品,并对采集的样品进行有机分析.在此基础上,针对公交车站候车的成年人群,应用美国EPA开发的电子数据库IRIS(Integrated Risk Information System),对可吸入颗粒物中的多环芳烃(PAHs)成分进行了健康风险评估.暴露采样的分析结果表明,两车站的PM10暴露浓度均值分别为(279.0±63.7)μg·m-3和(335.0±60.0)μg·m-3,其中的总多环芳烃质量浓度分别为(219.0±98.5)ng·m-3、(171.0±52.7)ng·m-3.多环芳烃致癌健康风险评估结果显示,两站候车人群在候车过程中的致癌风险分别为2.47×10-7、1.75×10-7,低于美国EPA所认可的可接受风险范围(10-6~10-4). 相似文献
84.
85.
86.
两种喹诺酮类抗生素对亚心形扁藻的毒性效应研究 总被引:1,自引:0,他引:1
研究了恩诺沙星和盐酸环丙沙星两种喹诺酮类抗生素对亚心形扁藻的毒理学效应。经多组不同浓度的两种抗生素处理后,分别对扁藻的96EC50、叶绿素和胞外聚合物(EPS)进行分析。结果表明,两种抗生素在低浓度时对扁藻生长具有促进作用,而在高浓度时体现抑制毒性作用。高浓度时,抗生素浓度越高对扁藻的生长、叶绿素和胞外聚合物抑制效果越明显,但当浓度达到一定高度后,抑制会达到其阈值。恩诺沙星和盐酸环丙沙星对扁藻的半生长抑制率分别为19.8 mg/L和28.7 mg/L。 相似文献
87.
88.
蚯蚓细胞色素P450酶系对土壤中芘或苯并[a]芘的响应 总被引:1,自引:0,他引:1
以赤子爱胜蚓(Eisenia fetida)为受试生物,通过人工污染草甸棕壤微宇宙试验方法,研究了暴露于不同环境浓度芘或苯并[a]芘(添加量分别为0.12、0.24、0.48、0.96 mg·kg~(-1))污染的土壤中14 d后,蚯蚓体内细胞色素P450(CYPs)酶系,如CYPs总量、CYP1A1及CYP2C9活性的变化.结果显示,芘或苯并[a]芘暴露导致蚯蚓CYPs总量、CYP1A1及CYP2C9活性的变化不同.其中,CYPs总量与CYP1A1活性对芘的响应趋势相似:试验3 d后,0.96 mg·kg~(-1)芘导致二者都显著高于对照水平;14 d后,都显著低于对照水平;CYP1A1活性对芘的响应更为敏感.CYPs总量与CYP2C9活性对苯并[a]芘的响应趋势相似:暴露初期,苯并[a]芘最高暴露剂量(0.96 mg·kg~(-1))导致二者都显著低于对照水平;试验结束后,苯并[a]芘最低暴露剂量(0.12 mg·kg~(-1))导致二者都显著高于对照水平,最高剂量暴露导致二者都显著低于对照水平,CYP2C9活性对苯并[a]芘的响应更为敏感.因此,推断CYPs亚酶对污染物的响应具有选择性且亚酶的响应敏感度高于CYPs总量.将CYPs总量与CYP1A1活性结合,或与CYP2C9活性结合分别诊断土壤芘污染或并[a]芘污染,较为准确有效. 相似文献
89.
90.
以南京某城市污水厂污水和污泥中的酞酸酯类(PAEs)为研究对象,分别采用固相萃取-气相色谱-质谱联用(SPE—Gc.Ms)和超声提取.气相色谱.质谱联用(USE—GC—Ms)检测其中的优先控制污染物邻苯二甲酸二甲酯(DMP)、邻苯二甲酸二乙酯(DEP)、邻苯二甲酸二丁酯(DBP)和邻苯二甲酸单(2-乙基己基)酯(MEHP),研究其在厌氧/好氧(A/O)污泥处理过程中的分布特征及降解规律。研究结果表明,各类PAEs在该污水厂的污水和污泥中均有检出,二级处理出水中4种酞酸酯类物质的浓度在0.151—2.419μg/L。污水中4种酞酸酯的分布规律为MEHP〉DBP〉DMP〉DEP,污泥中4种酞酸酯的分布规律为MEHP〉DBP〉DEP〉DMP。该污水厂二级处理工艺对4种PAEs的去除效果较明显,去除效率DBP〉DEP〉DMP〉MEHP. 相似文献