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Lihui Huang Chang Ho Yu Philip K. Hopke Jin Young Shin 《Journal of the Air & Waste Management Association (1995)》2014,64(12):1439-1445
Measurement of carcinogenic Cr(VI) in ambient PM is challenging due to potential errors associated with conversion between Cr(VI) (a carcinogen) and Cr(III) (an essential nutrient). Cr(III) conversion is a particular concern due to its >80% atomic abundance in total Cr. U.S. Environmental Protection Agency (EPA) method 6800 that uses water-soluble isotope spikes can be used to correct the interconversion. However, whether the enriched Cr(III) isotope spikes can adequately mimic the Cr(III) species originally in ambient PM is unknown. This study examined the water solubility of Cr(III) in ambient PM and discussed its influence on Cr(VI) measurement. Ambient PM10 samples were collected on Teflon filters at four sites in New Jersey that may have different Cr emission sources. The samples were ultrasonically extracted with 5 mL DI-H2O (pH 5.7) at room temperature for 40 min, and then analyzed by ion chromatography–inductively coupled plasma mass spectrometry (IC-ICPMS). Cr(III) was below detection limit (0.06 ng/m3) for all samples, suggesting water-soluble Cr(III) species, such as CrCl3, Cr(NO3)3, and amorphous Cr(OH)3, in the ambient PM were negligible. Therefore, the enriched 50Cr(III) isotope spike (in the form of Cr(NO3)3) could not mimic the original ambient Cr(III). Only the conversion of 53Cr(VI) (in the form of K2CrO4) was taken into account when correcting the interconversion. We then used NaHCO3-pretreated MCE filters (prespiked with enriched isotope species) to measure Cr(VI) in the ambient PM10. The samples were ultrasonically extracted at 60 C pH 9 solutions for 40 min followed by IC-ICPMS analysis. Due to the correction of Cr(VI) reduction, the Cr(VI) concentrations determined by EPA method 6800, 0.26 ± 0.16 (summer) and 0.16 ± 0.11(winter) ng/m3 (n = 64), were significantly greater than those by the external standard curve, 0.21 ± 0.17 (summer) and 0.10 ± 0.07 (winter) ng/m3 (n = 56) (p < 0.01, Student’s t-test). Our study revealed that appropriate application of EPA method 6800 is important because it only applies to soluble fraction of Cr species in ambient PM.
ImplicationsAccurate measurement of carcinogenic Cr(VI) in ambient PM is challenging due to conversion between Cr(VI) (a human carcinogen) and Cr(III) (a human essential nutrient). The conversion of Cr(III) is of particular concern due to its dominant presence in total Cr (>80%). This study examined the water solubility of Cr(III) in ambient PM that was collected at four locations in New Jersey. Then we discussed the influence of Cr(III) solubility on the application of EPA method 6800, which utilizes enriched isotope spikes to correct the interconversion. Our results suggested that appropriate application of EPA method 6800 is important because it only applies to soluble fraction of Cr species. 相似文献
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住宅室内降尘中邻苯二甲酸酯的污染特征及传输途径 总被引:1,自引:0,他引:1
本文分别于夏季和冬季在北京市40户家庭的客厅和卧室采集降尘样品,研究降尘中邻苯二甲酸酯(PAEs)的污染特征.结果表明,室内降尘中主要的PAEs(及其浓度)为DIBP (39.6 ng·mg~(-1),几何平均浓度,下同)、DBP (38.7 ng·mg~(-1))和DEHP (418.5 ng·mg~(-1)).降尘中PAEs的浓度与温度、相对湿度和换气次数均呈显著正相关(P0.005).这是由于室温升高和换气次数增高加快PAEs的源排放速率,促进室内空气中PAEs积累并通过气相媒介传输使得降尘PAEs浓度增高;湿度升高促进空气中PAEs向降尘的传质,增大降尘中PAEs浓度.3种因素共同影响使得夏季降尘中3种PAEs的浓度均显著高于冬季(P0.0001).研究还发现,源材料中PAEs至降尘的传输途径包括以气相为媒介的间接传输和源至降尘的直接转移,因此降尘PAEs浓度与采集平面材料相关;降尘PAEs浓度还受降尘在室内的停留时间影响.因此,相关研究需指明降尘的类型、采集位置和平面材料,便于利用测量数据进行准确的暴露评估. 相似文献
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铜绿假单胞菌NY3所产表面活性剂对原油降解的影响 总被引:1,自引:0,他引:1
铜绿假单胞菌NY3是从石油污染土壤中分离出的一株能快速代谢疏水性化合物的菌种。研究了该菌产表面活性剂及对原油降解的作用。实验表明,在敞开体系中,投加82 mg/L NY3菌产的鼠李糖脂,240 h能使NY3对原油的降解率提高50%。投加甘油使NY3产鼠李糖脂与降解原油同步进行,与投加鼠李糖脂对原油降解的促进作用相近。投加9‰甘油使NY3在168 h对原油的降解率提高43%。NY3菌能同时降解原油中的直链烷烃及菲(Pr)和芘(Ph)等多环芳烃。在敞开体系中用少量甘油使产鼠李糖脂和降解原油同步进行,节约处理费用。研究结果为NY3菌株在露天石油污染环境修复中的应用奠定了基础。 相似文献
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