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831.
以硅藻土为载体,采用溶胶-凝胶法引入金属氧化物SnO2和Fe2O3,制备了二元氧化物复合型SO42-/SnO2-Fe2O3-硅藻土固体酸催化剂。利用该催化剂与H2O2构成非均相类Fenton试剂氧化体系,催化H2O2产生氧化能力极强的·OH,用于处理实际翠蓝废水和模拟亚甲基蓝废水。催化剂的最佳制备条件为:H2SO4溶液的浓度3 mol/L,浸渍时间2.0 h,焙烧温度550 ℃,焙烧时间3.5 h,焙烧方式为随炉升降温。实验结果表明:采用在最佳工艺条件下制得的催化剂,处理实际翠蓝废水COD去除率可达79.5%、脱色率达99.6%;处理模拟亚甲基蓝废水COD去除率可达83.1%、脱色率达99.6%。  相似文献   
832.
运用GC-MS、紫外光谱及三维荧光光谱扫描技术考察了石化污水处理厂“水解酸化—厌氧处理—好氧处理”工艺的各单元出水中有机污染物的变化情况。总进水中检出84种主要有机污染物,主要含有烃类27种,酚类5种,醛、酯、醇和酮类化合物共24种,胺类4种,腈、有机酸及其他杂环化合物14种,另有10种物质未定性;该工艺的COD累积去除率达87.66%, 64种有机污染物被完全去除,17种有机污染物去除率可达90%以上,接触氧化池出水中主要含杂环化合物和少量醛、醇、酯类化合物。  相似文献   
833.
王佳  李安峰  潘涛  骆坚平 《化工环保》2014,34(4):352-355
利用两相厌氧工艺处理高浓度丙烯酸生产废水。实验结果表明:在较高进水COD和容积负荷的条件下,系统具有良好、稳定的处理效果;在负荷提高及稳定运行阶段,将生活污水与丙烯酸生产废水的体积比调整为5∶1,容积负荷最大提高至12.3 kg/(m3·d),两相厌氧反应器可长期稳定运行,总COD去除率基本维持在90%以上,出水COD小于323 mg/L;当进水甲醛质量浓度为800~1 733 mg/L时,总甲醛去除率基本稳定在95.6%~99.3%;在负荷提高及稳定运行阶段,水解酸化相反应器和产甲烷相反应器的出水pH分别为6.2~7.6和7.6~8.1,出水总碱度分别为1 220~1 820 mg/L和1 800~2 620 mg/L。  相似文献   
834.
Fruit, vegetable, flower waste (FVFW), dairy products waste (DPW), meat waste (MW) and sugar waste (SW) obtained from a supermarket chain were anaerobically digested, in order to recover methane as a source of renewable energy. Batch mesophilic anaerobic reactors were run at total solids (TS) ratios of 5%, 8% and 10%. The highest methane yield of 0.44 L CH4/g VSadded was obtained from anaerobic digestion of wastes (FVFW + DPW + MW + SW) at 10% TS, with 66.4% of methane (CH4) composition in biogas. Anaerobic digestion of mixed wastes at 5% and 8% TS provided slightly lower methane yields of 0.41 and 0.40 L CH4/g VSadded, respectively. When the wastes were digested alone without co-substrate addition, the highest methane yield of 0.40 L CH4/g VSadded was obtained from FVFW at 5% TS. Generally, although the volatile solids (VS) conversion percentages seemed low during the experiments, higher methane yields could be obtained from anaerobic digestion of supermarket wastes. A suitable carbon/nitrogen (C/N) ratio, proper adjustment of the buffering capacity and the addition of essential trace nutrients (such as Ni) could improve VS conversion and biogas production yields significantly.  相似文献   
835.
As far as the optimal design, operation, and field application of the Aerobic–Anaerobic Landfill Method (AALM) are concerned, it is very important to understand how aeration modes (different combinations of aeration depth and air injection rate) affect the biodegradation of organic carbon and the transformation of nitrogen in landfill solid waste. Pilot-scale lysimeter experiments were carried out under different aeration modes to obtain detailed information regarding the influence of aeration modes on leachate characteristics. Results from these lysimeter experiments revealed that aeration at the bottom layer was the most effective for decomposition of organic carbon when compared with aeration at the surface or middle layers. Moreover, the air injection rate led to different nitrogen transformation patterns, unlike the lesser influence it has on organic carbon decomposition. Effective simultaneous nitrification and denitrification were observed for the aeration mode with a higher air injection rate (=1.0 L/min). On the other hand, the phenomenon of sequenced nitrification and denitrification could be observed when a low air injection rate (=0.5 L/min.) was employed. Finally, it is concluded that, for AALM, air injection with a higher air injection rate at the deepest layer near the leachate collection pipe tends to accelerate the stabilization of landfill waste as defined in terms of the enhancement of denitrification as well as organic carbon decomposition.  相似文献   
836.
The anaerobic digestion of municipal sewage sludge (SS) with swine manure (SM) and poultry manure (PM) was undertaken. It was found that a mixture of sewage sludge with a 30% addition of swine manure gave around 400 dm3/kgVS of biogas, whereas the maximal biogas yield from ternary mixture (SS:SM:PM = 70:20:10 by weight) was only 336 dm3/kgVS. An inhibition of methanogenesis by free ammonia was observed in poultry manure experiments. The anaerobic digestion was inefficient in pathogen inactivation as the reduction in the number of E. coli an Enterobacteriaceae was only by one logarithmic unit. A substantial portion of pathogens was also released into the supernatant.  相似文献   
837.
The production of compost and digestate from source-separated organic residues is well established in Europe. However, these products may be a source of pollutants when applied to soils. In order to assess this issue, composts, solid and liquid digestates from Switzerland were analyzed for heavy metals (Cd, Co, Cr, Cu, Ni, Pb and Zn) addressing factors which may influence the concentration levels: the treatment process, the composition, origin, particle size and impurity content of input materials, the season of input materials collection or the degree of organic matter degradation.Composts (n = 81) showed mean contents being at 60% or less of the legal threshold values. Solid digestates (n = 20) had 20–50% lower values for Cd, Co, Pb and Zn but similar values for Cr, Cu and Ni. Liquid digestates (n = 5) exhibited mean concentrations which were approximately twice the values measured in compost for most elements. Statistical analyses did not reveal clear relationships between influencing factors and heavy metal contents. This suggests that the contamination was rather driven by factors not addressed in the present study.According to mass balance calculations related to Switzerland, the annual loads to agricultural soils resulting from the application of compost and digestates ranged between 2% (Cd) and 22% (Pb) of total heavy metal loads. At regional scale, composts and digestates are therefore minor sources of pollution compared to manure (Co, Cu, Ni, Zn), mineral fertilizer (Cd, Cr) and aerial deposition (Pb). However, for individual fields, fertilization with compost or digestates results in higher heavy metal loads than application of equivalent nutrient inputs through manure or mineral fertilizer.  相似文献   
838.
The study was carried out to assess the levels of pesticide residues in the water of Meiliangwan Bay, Taihu Lake of China. The most commonly employed organochlorine pesticides (OCPs), organophosphorus pesticides (OPPs) and herbicide atrazine were analyzed. The water samples were collected seasonally from Meiliangwan Bay within a period of one year. The pesticides were analyzed by gas chromatography (GC) with μECD or NPD after solid-phase extraction (SPE), which was confirmed by GC with an ion trap mass spectrometry (MS). The mean concentrations were 1.98 ng/l for lindane, 0.378 ng/l for heptachlor epoxide, 0.367 ng/l for p,p′-DDE, 0.496 ng/l for p,p′-DDD, 1.06 ng/l for p,p′-DDT and 51.6 ng/l for dichlorvos, 39.0 ng/l for demeton, 346 ng/l for dimethoate, 4.12 ng/l for methyl parathion, 11.6 ng/l for malathion, 2.17 ng/l for parathion and 217 ng/l for atrazine. Generally, low concentrations of OCP were found, whereas the concentrations of the OPPs and atrazine in the water of Taihu Lake were relatively high. Heptachlor epoxide and lindane were the two most commonly encountered OCPs while dichlorvos, demeton and dimethoate were found to have much higher concentrations and occurrences than other OPPs.  相似文献   
839.
Abstract

Fensulfothion was incubated in nutrient media with a mixed culture of soil microorganisms obtained from sandy loam. The half life of fensulfothion in both inoculated samples and sterile controls was about 16 wk. There was some conversion to fensulfothion sulfone (16% at 6 wk) in inoculated samples, but not in the controls. Traces of fensulfothion sulfide were found in both inoculated samples (<3%) and controls (<2%) . When 1% ethanol was added to the inoculated nutrient mixture the fensulfothion disappeared rapidly (t½>~1½> wk) with 32% conversion at 20 wk to fensulfothion sulfide.  相似文献   
840.
Abstract

An improved Gas Chromatographic method utilizing simple extraction and one‐step purification on solid phase extraction tubes was developed for analysis of trichlorfon as an intact insecticide compound in turfgrass thatch and soil. A Gas Chromatograph/Mass Spectrum (GC/MS) was used for confirmation of trichlorfon structure. The method readily determines trichlorfon in the presence of dichlorvos. Using an electron capture (EC) detector, the detection limits were 0.02 ppm in soil, 0.04 ppm in turfgrass thatch, and 0.09 ppm in soil, and 0.2 ppm in turfgrass thatch using an nitrogen phosphorus (NP) detector.  相似文献   
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