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591.
通过在不同pH值,温度等条件下Ca5(AsO4)3OH的溶解,确定其稳定存在的pH值范围,得出它的溶度积和生成的自由能(ΔG0f)。结果表明,Ca5(AsO4)3OH在水中的溶解度和稳定范围与pH和温度有关,在酸性条件下(初始pH=2)它的溶解度较大,而且在水中的溶解度随着温度的升高而降低。利用PHREEQC程序计算确定Ca5(AsO4)3OH的溶度积为10-40.86,生成自由能ΔG0f为-5 063.53 kJ/mol。利用JADE5软件计算得到其晶格参数a=b=9.696,c=6.967和晶胞体积为567.304 3。 相似文献
592.
采用水热法制备出LiFePO4催化剂,通过电子显微镜(SEM)、X射线衍射(XRD)和傅立叶红外光谱(FTIR)对其进行表征,并将其作为非均相Fenton催化剂处理亚甲基蓝(MB)染料溶液。实验结果表明,在催化剂用量为4 g/L,H2O2浓度为0.04 mol/L,pH值为3,温度为50℃,反应时间为60 min的条件下,浓度为500 mg/L的亚甲基蓝脱色率达99%。根据实验结果,讨论了LiFePO4作为非均相Fenton催化剂对亚甲基蓝的降解机理。 相似文献
593.
This paper discusses the current state and future prospects of backward production linkages to the manufacturing sector in the Angolan oil and gas industry. The paper finds that local value-added links are currently limited to labour and to a lesser degree in basic services. However, there is a realistic and strategic potential for local manufacturing linkages to expand in the oilfield services sector of the industry, which in turn can stimulate industrial development. For this to be achieved, the factors that are currently constraining the expansion and deepening of linkages have to be addressed, namely, a weak local content strategy, a weak local skills and industrial base and the integration of industrial and oil sector policies. 相似文献
594.
595.
UASB反应器中厌氧氨氧化菌的影响因素研究 总被引:3,自引:0,他引:3
在UASB反应器中接种实验室已经驯化好的厌氧氨氧化颗粒污泥,对其进行厌氧氨氧化菌活性提高和影响因素的实验研究。研究表明厌氧氨氧化菌对NH4+-N和N02--N的适宜浓度负荷均为200mg/L,适宜水力停留时间HRT、温度、pH和进水基质比(N02--N/NH4+-N)分别为2h、30~35℃、7.5~8.5和0.95~1.2,NH4+-N、NO2--N和TN的平均去除率分别为97.1%、98.3%和92.7%。 相似文献
596.
597.
临安区域本底站大气甲烷浓度变化特征 总被引:1,自引:0,他引:1
通过分析2006年8月~2009年7月临安区域大气本底站Flask瓶采样获得的CH4浓度特征,结合地面风向、后向轨迹、排放清单,研究了CH4浓度变化特征和长三角地区排放源对CH4浓度的影响作用。结果表明,临安区域大气本底站的CH4浓度分布在1 7584×10-9~1 9700×10-9,具有较明显的季节波动变化特征,浓度季节变化幅度为737×10-9;CH4浓度平均年增幅达176×10-9,增速较快。东北风和东南风时,CH4浓度较高;西南风时CH4浓度较低。导致CH4高浓度分布的气团主要来自临安站的东北、偏东方向;导致CH4低浓度分布的气团集中在西南 偏南 相似文献
598.
Cartaxo MA Ablad K Douch J Berghoute Y Hamdani M Mendonça MH Nogueira JM Pereira MI 《Chemosphere》2012,86(4):341-347
Fe-Co3O4 thin film with different amounts of Fe have been used for the electro-oxidation of phenol in alkaline medium at room temperature. The electrodes were prepared by coating stainless steel supports with successive layers of the oxides, obtained by thermal decomposition at 673 K. The electrolysis was carried out at constant potential and the phenol disappearance, during the electrolysis, was monitored by UV-Vis absorbance measurements between 250 and 500 nm. After 3 h of electrolysis, the intermediates were identified by comparing the HPLC data and UV-Vis spectra to those from pure standards. The results indicate that the same oxidation products are formed on the different prepared electrodes, namely the decomposition products of phenol such as benzoquinone, hydroquinone and cathecol in basic medium. Simulated results show clearly the decrease of the amount of phenolic species with the electrolysis time. An enhancement of the phenol removal is observed with the presence of iron in the oxide. Under the operating conditions, around 30% of the initial phenol has been removed at ca. 3 h and the complete degradation is obtained after 54 h of electrolysis, when Fe-Co3O4 thin film with 10% of Fe is used as anode. 相似文献
599.
In this work, Bi4NbxTa(1−x)O8I photocatalysts have been synthesized by solid state reaction method and characterized by powder X-ray diffraction, scanning electron microscope and UV-Vis near infrared diffuse reflectance spectroscopy. The photocatalytic activity of these photocatalysts was evaluated by the degradation of methyl orange (MO) in aqueous solutions under visible light, UV light and solar irradiation. The effects of catalyst dosage, initial pH and MO concentration on the removal efficiency were studied, and the photocatalytic reaction kinetics of MO degradation as well. The results indicated that Bi4NbxTa(1−x)O8I exhibited high photocatalytic activity for the removal of MO in aqueous solutions. For example, the removal efficiency of MO by Bi4Nb0.1Ta0.9O8I was as high as 92% within 12 h visible light irradiation under the optimal conditions: initial MO concentration of 5-10 mg L−1, catalyst dosage of 6 g L−1 and natural pH (6-8), the MO molecules could be completely degradated by Bi4Nb0.1Ta0.9O8I within 40 min under UV light irradiation, and the photodegradation efficiency reaches to 60% after 7 h solar irradiation. Furthermore, the photocatalytic degradation of Bisphenol A (BPA) was also investigated under visible light irradiation. It is found that 99% BPA could be mineralized by Bi4Nb0.1Ta0.9O8I after 16 h visible light irradiation. Through HPLC/MS, BOD, TOC, UV-Vis measurements, we determined possible degradation products of MO and BPA. The results indicated that MO was degradated into products which are easier to be biodegradable and innocuous treated, and BPA could be mineralized completely. Furthermore, the possibility for the photosensitization effect in the degradation process of MO under visible light irradiation has been excluded. 相似文献
600.
4A沸石对复合污染水体中Pb2+、Cu2+和Cd2+的去除 总被引:2,自引:2,他引:0
采用静态吸附法以4A沸石为吸附剂研究其对复合污染水体中Pb2+、Cu2+和Cd2+的竞争吸附特性,并探讨了影响吸附的环境因素。实验表明,在室温条件下,溶液pH5~6,4A沸石15 mg对10 mL复合污染溶液(Pb2+、Cu2+和Cd2+浓度分别为100 mg/L)吸附20 min时,对溶液中3种重金属的吸附去除率均可达99.8%以上。反应过程中4A沸石对3种重金属的吸附速率大小为Pb2+>Cu2+>Cd2+。复合污染水体中4A沸石对Pb2+、Cu2+和Cd2+的吸附符合Langmuir和Fre-undlich等温吸附方程,相关系数分别为0.9981、0.9901、0.9916和0.9638、0.9194、0.9689。经计算,4A沸石对Pb2+、Cu2+和Cd2+的饱和吸附量分别为129.9 mg/g、107.5 mg/g和99.0 mg/g。4A沸石吸附重金属离子达到吸附平衡的时间较短,对溶液pH值的适应性较好。吸附后的4A沸石可以再生利用,对铅离子洗脱重复利用性较铜离子和镉离子强。 相似文献