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81.
Sun JM Zhu WT Huang JC 《Environmental science and pollution research international》2006,13(6):379-385
BACKGROUND, AIMS AND SCOPE: Hexavalent chromium [Cr(VI)] cannot react with either carbonate or hydroxide to form chromium precipitates. However, by using a precipitation technology to treat plating wastewater containing Cr(VI), Cu(II), Ni(II) and Zn(II), approximately 78% of Cr(VI) (initial 60 mg/L) was co-removed with the precipitation of Cu(II), Ni(II) and Zn(II) (each 150 mg/L) by dosing with Na2CO3 (Sun 2003). Direct precipitation by forming Cu(II)-Cr(VI) precipitates followed by adsorption of Cr(VI) onto freshly formed Cu-precipitates was subsequently found to be the main mechanism(s) involved in Cr(VI) co-removal with Cu(II) precipitation by dosing Na2CO3 stepwise to various pH values (Sun et al. 2003). This study was. carried out to further characterize the formation of primary precipitates during the early stages of copper precipitation and simultaneous removal of Cr(VI) with Cu(II). METHODS: Test metal-solutions were prepared with industrial grade chemicals: CuCl2 x 2H2O, Na2SO4 and K2Cr2207. NaCO3 was added drop-wise to synthetic metal-solution to progressively increase pH. For each pH increment, removal of soluble metals was detected by atomic absorption spectrophotometer (AAS) and surface morphology of precipitates was analyzed by scanning electron microscope (SEM). To further characterize the formation of primary precipitates, a series of MINEQL+ thermodynamic calculations/analyses and equilibrium calculations/ analyses were conducted. RESULTS AND DISCUSSION: MINEQL+ thermodynamic calculation indicated that, for a system containing 150 mg/L Cu(II) and 60 mg/L Cr(VI) with gradual Na2CO3 dosing, if any precipitates can be formed at pH 5.0 or lower, it should be in the form of CuCrO4. Comparison tests using systems containing the same equivalent of Cu(II) plus Cr(VI) and Cu(II) plus SO4(2-) showed that the precipitation occurred at a pH of around 5.0 in the Cu(II)-Cr(VI) system and around 6.0 in the Cu(II)-SO4(2-) system. The discrepancy of the precipitation was indeed caused by the formation of Cu-Cr precipitates. The initiation of copper removal at pH around 5.0 for the Cu-Cr co-removal test was not attributable to the formation of Cu-CO3 precipitates, instead, it was most likely through the formation of insoluble Cu-Cr precipitates, such as CuCrO4 and CuCrO4 x 2Cu(OH)2. Experimental tests, equilibrium calculations, MINEQL+ thermodynamic calculations and surface morphologies for systems using higher concentrations of Cu(II) and Cr(VI) further verified the most probable composition of primary precipitates is copper-chromate. CONCLUSION: In the Cu-Cr co-removal test with Na2O3 dosing to increase pH and induce metal precipitation, copper-chromate precipitates are the primary precipitates produced and contribute to the initial simultaneous removal of copper and chromium. 相似文献
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简述了水煤浆加压气化制合成氨系统的特点,着重介绍了该系统制气工段和净化工段的三废排放情况及治理措施,并对仍存在的问题提出了看法。 相似文献
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Leila G. Rhue Mitchell J. Small 《Journal of the American Water Resources Association》1986,22(1):121-127
ABSTRACT: The application of a low-flow assessment model is illustrated for the Monogahela River Basin. The model simulates the impact of reservoir operating rules and consumptive use limitation policies on low-flow frequency at downstream locations in the basin. Policies are evaluated using an observed flow sequence and synthetic flow inputs. The paper reviews the historical development of flow management on the Monogahela to provide background for the current study. 相似文献
87.
提出了用于水处理的Ca(OH)_2-PDADMA-PAM新方法,采用核法对兰州制革厂综合废水进行絮凝处理的研究.实验结果表明,该法对污染物的去除率高,絮凝剂用量少,沉降速度快,产生的污泥量小,并对多种水质的处理具有适用性. 相似文献
88.
自动增氧型潜流人工湿地处理农村生活污水的研究 总被引:43,自引:0,他引:43
采用人工配水模拟太湖地区农村生活污水水质,利用改进的自动增氧型潜流人工湿地对其进行处理,结果表明:COD、NH4 -N、TP进水浓度分别在132.4~392.6mg·L-1、21.58~50.26mg·L-1、3.60~13.17mg·L-1范围内变化时,COD、NH4 -N、TP的去除负荷随着进水浓度的升高而增大,其最高去除负荷分别为226.38 kg·d-1·hm-2、44.40 kg·d-1·hm-2、10.44 kg·d-1·hm-2,相应的去除率为89.45%、88.93%、90.25%,且系统有较强的抗冲击负荷能力. 相似文献
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Monitoring of Pesticide Residues in Fruits 总被引:1,自引:0,他引:1
Fruit samples of ber, grapes and guava analysed for pesticide residues employing multiresidue analysis by gas liquid chromatography equipped with ECD and NPD detectors and capillary columns showed contamination with organochlorine, synthetic pyrethroid and organophosphate insecticides. Among organochlorines, HCH, DDT and endosulfan were detected in almost all the samples. Residues of HCH and DDT were maximum in ber followed by grapes and guava where as of endosulfan were maximum in guava followed by grapes and ber. All the fruit samples showed the presence of residues with one or the other group of pesticides. Residues of none of the pesticides exceeded the MRL values in any sample. On the basis of these studies, it is suggested that monitoring studies should be extended to other fruits grown in different agro climatic regions which may serve as basis for future policy in chemical use. 相似文献