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241.
考察了不同粒径零价铁(ZVI),包括200目普通铁粉(200m-ZVI)、800目超细铁粉(800m-ZVI)和纳米铁粉(nZVI,粒径=20 nm),对污水污泥的硫化氢和甲烷释放速率的影响。研究发现:(1)在22 d内,添加0.1%的200m-ZVI使污泥的硫化氢释放速率提高48.0%,而添加0.1%的800-ZVI和nZVI,则使污泥的硫化氢释放速率分别降低33.1%和77.1%;(2)不同粒径ZVI均可以提高污泥沼气中的甲烷浓度,且依次为nZVI〉800m-ZVI〉200m-ZVI;(3)在23 d内,添加0.1%的200m-ZVI和nZVI使污泥的甲烷累计产生量分别提高了15.5%和40.6%,而添加0.1%800m-ZVI则使甲烷产生量降低了12.5%。nZVI可以有效控制污泥的硫化氢释放,并显著提升污泥在厌氧发酵过程的产甲烷速率。 相似文献
242.
采用间歇式摇床试验,研究了葡萄糖共基质条件下Fe^0-厌氧微生物体系中Fe^0投加量、pH值、染料初始浓度对活性艳红X-3B模拟废水脱色率的影响,比较了Fe^0-厌氧微生物、纯厌氧微生物及纯Fe^0 3种体系中废水的脱色效果。结果表明:Fe^0-厌氧微生物体系中初始浓度(50~500mg/L)对活性艳红X-3B的脱色率影响不大;而Fe^0投加量、pH值存在一个最佳范围;当Fe^0投加量为260mg/L,pH值为6.0,污泥浓度为0.35gVSS/L,停留时间约为30h时,体系中活性艳红X-3B的脱色率可达90%左右,比相同试验条件下纯Fe^0、纯厌氧微生物体系达到此脱色率所需时间分别缩短了约1/2、7/10。在Fe^0-厌氧微生物体系中,由紫外可见分光光度分析可推测活性艳红X-3B的脱色机理主要是其偶氮键发生断裂,生成苯胺和萘类物质,而且苯胺和萘类物质能得到进一步降解。 相似文献
243.
Yu Ren Aijun Ding Tao Wang Xinhua Shen Jia Guo Jiamin Zhang Yan Wang Pengju Xu Xinfeng Wang Jian Gao Jeffrey L. Collett 《Atmospheric environment (Oxford, England : 1994)》2009,43(9):1702-1711
Measurement of ambient gas-phase total peroxides was performed at the summit of Mount Tai (Mt. Tai, 1534 m above sea level) in central-eastern China during March 22–April 24 and June 16–July 20, 2007. The hourly averaged concentration of peroxides was 0.17 ppbv (± 0.16 ppbv, maximum: 1.28 ppbv) and 0.55 ppbv (± 0.67 ppbv, maximum: 3.55 ppbv) in the spring and summer campaigns, respectively. The average concentration of peroxides at Mt. Tai, which is in a heavily polluted region, was much lower than hydrogen peroxide measurements made at some rural mountain sites, suggesting that significant removal processes took place in this region. An examination of diurnal variation and a correlation analysis suggest that these removal processes could include chemical suppression of peroxide production due to the scavenging of peroxy and hydroxy radicals by high NOx, wet removal by clouds/fogs rich in dissolved sulfur dioxide which reacts quickly with peroxides, and photolysis. These sinks competed with photochemical sources of peroxides, resulting in different mean concentrations and diurnal pattern of peroxides in the spring and summer. A principal component analysis was conducted to quantify the major processes that influenced the variation of peroxide concentrations. This analysis shows that in the spring photochemical production was an important source of peroxides, and the major sink was scavenging during upslope transport of polluted and humid air from the lower part of the planetary boundary layer (PBL) and wet removal by synoptic scale clouds. During the summer, highly polluted PBL air (with high NOx) was often associated with very low peroxides due to the chemical suppression of HO2 by high NOx and wet-removal by clouds/fogs in this sulfur-rich atmosphere, especially during the daytime. Higher concentrations of peroxides, which often appeared at mid-nighttime, were mainly associated with subsidence of air masses containing relatively lower concentrations of NOy. 相似文献
244.
Songjun Guo Sheng Wen Xinming Wang Guoying Sheng Jiamo Fu Ping Hu Yingxin Yu 《Atmospheric environment (Oxford, England : 1994)》2009,43(22-23):3489-3495
Formaldehyde and acetaldehyde are two most abundant carbonyls in ambient air. Biogenic emission has been proposed as a significant source other than anthropogenic emissions and atmospheric secondary formation. Here at a forest site in South China, the carbon isotopic compositions of formaldehyde and acetaldehyde emitted from leaves of three tree species (Litsea rotundifolia, Canarium album and Castanea henryi) were measured in comparison with the bulk carbon isotopic compositions of tree leaves. δ13C data of the emitted aldehydes (from ?31‰ to ?46‰) were quite different for tree species, which were all more depleted in 13C than the tree-leaf bulk δ13C values (from ?27‰ to ?32‰). Formaldehyde in ambient air at the forest site had δ13C values different from those of leaf-emitted formaldehyde, indicating other sources for ambient formaldehyde apart from direct emission from leaves, most probably the photooxidation of biogenic hydrocarbon like isoprene and monoterpene. The δ13C differences of acetaldehyde between ambient data and those of tree leaves emission were less than 1‰, implying direct biogenic emission as the dominant source. 相似文献
245.
微波诱导AC/Cu、AC/Fe催化非均相Fenton 反应催化降解垃圾渗滤液 总被引:1,自引:0,他引:1
采用活性炭载体负载Cu、Fe为催化剂,在微波诱导作用下,对垃圾渗滤液污染物进行降解。实验结果表明,活性炭负载金属前经适当浓度硝酸浸泡处理后,催化剂对COD去除率提高可超过15%,过高硝酸盐浓度对COD去除有不利影响;催化剂对COD去除率随Cu、Fe金属负载量增加呈先增加后降低的趋势,催化剂对Cu、Fe的最佳负载量分别为质量百分比2.11%和1.12%。对于AC-Cu体系,在初始pH=3,H2O2投加量为4.98×103mg/L,催化剂用量为5.0×103mg/L,420 W功率下微波辐射10 min时,垃圾渗滤液COD去除率可达到84.13%;对于AC-Fe体系,当H2O2投加量为0.33×103mg/L,催化剂AC-Fe用量为2.0×104mg/L,420 W功率下微波作用10 min时,垃圾渗滤液COD去除率为60.16%。分析2种催化剂对COD去除差异的原因,可能是催化剂AC-Cu表面单分子分布的阈值比AC-Fe高。降解液的pH值对AC-Cu体系、AC-Fe体系COD去除影响存在拐点,最高COD去除率点对应的降解液pH值为3。微波辐射功率较低时,体系COD去除率随辐射功率增加而增加;辐射功率较高时,高温下垃圾渗滤液中有机硫化物分解成小分子硫化物,对催化剂活性存在一定抑制作用。 相似文献
246.
Heterogeneous photocatalytic degradation of methyl orange in schwertmannite/oxalate suspension under UV irradiation 总被引:1,自引:0,他引:1
Wu Y Guo J Jiang D Zhou P Lan Y Zhou L 《Environmental science and pollution research international》2012,19(6):2313-2320
Introduction
Schwertmannite was synthesized through an oxidation of FeSO4 by Acidithiobacillus ferrooxidans LX5 cell suspension at an initial pH?2.5 and 28°C for 3?days and characterized using X-ray diffraction spectroscopy and scanning electron microscope. The schwertmannite photocatalytic degradation of methyl orange (MO) by oxalate was investigated at different initial pH values, concentrations of schwertmannite, oxalate, and MO.Results
The results demonstrated that photodegradation of MO in the presence of schwertmannite or oxalate alone was very weak. However, the removal of MO was significantly enhanced when schwertmannite and oxalate coexisted in the reaction system. Low pH (4 or less) was beneficial to the degradation of MO. The optimal doses of schwertmannite and oxalate were 0.2?g?L?1 and 2?mM, respectively. Hydroxyl radicals (·OH) and Fe(II), the intermediate products, were also examined during the reaction to explore their correlation with the degradation of MO.Conclusion
A possible mechanism for the photocatalytic decomposition of MO in the study was proposed. The formation of Fe(III)-oxalate complexes on the surface of schwertmannite was a precursor of H2O2 and Fe(II) production, further leading to the yield of ·OH responsible for the decomposition of MO. 相似文献247.
Yuan-Na Xing Ying Guo Mei Xie Ru-Lang Shen 《Environmental pollution (Barking, Essex : 1987)》2009,157(4):1382-1387
A solid-phase microextration-based sampling method was employed to determine the concentrations of 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane (DDT) and its metabolites, 1,1-dichloro-2,2-bis(p-chlorophenyl)ethane (DDD), 1,1-dichloro-2,2-bis(p-chlorophenyl)ethene (DDE) and 1-chloro-2,2-bis(p-chlorophenyl)ethene (DDMU), in two estuarine bays, Daya Bay and Hailing Bay, of South China. Six DDT components including p,p′-DDT, o,p′-DDD, p,p′-DDD, o,p′-DDE, p,p′-DDE, and p,p′-DDMU were detected in Hailing Bay, while only p,p′-DDD was found in Daya Bay. p,p′-DDD was the most abundant DDT component in both bays, sharply different from the previous finding in the water column of the Palos Verdes Shelf, California, USA that p,p′-DDE was prevalent. In addition, the occurrence of p,p′-DDMU (with a range of 0.047-0.21 ng/L in Hailing Bay) has not been reported around the globe, and its presence in our study region appeared to stem from dehydrochlorination of p,p′-DDD, favored under aerobic conditions, but further investigations are clearly needed to confirm the mechanism for generation of DDMU in estuarine environments. 相似文献
248.
Ying Guo Huan-Yun Yu Eddy Y. Zeng 《Environmental pollution (Barking, Essex : 1987)》2009,157(6):1753-1763
This review summarizes and analyzes available data in the literature (mostly after 2000) on the occurrence of dichlorodiphenyltrichloroethane (DDT) and its main metabolites, dichlorodiphenyldichloroethane (DDD) and chlorodiphenyldichloroethylene (DDE), in the environment of the Pearl River Delta (PRD), South China. Generally, the concentration levels of the sum of DDT, DDD, and DDE, designated as DDTs thereafter, have not significantly declined since 1983. However, the composition of DDTs residues has changed with time. DDTs in soil, freshwater sediment and freshwater fish species were mainly residues from chronological use. There is evidence that new point sources, such as dicofol and anti-fouling paint, may have contributed DDTs to various environmental compartments. Risk assessment against existing criteria indicated that the levels of DDTs in water and some fish species may pose adverse effects to humans or wildlife, and those in sediment/soil may also cause negative impacts to the eco-environment of the PRD. 相似文献
249.
EDTA络合铜在无机柱撑膨润土上的吸附研究 总被引:1,自引:1,他引:1
利用天然膨润土、羟基铁和羟基铁铝柱撑膨润土,进行吸附EDTA络合铜离子(EDTA-Cu)的实验.研究了溶液中EDTA与Cu2 摩尔比、pH值、吸附时间对吸附过程的影响和吸附等温线的变化规律.结果表明,达到吸附平衡的时间为1 h;pH值对天然膨润土的吸附影响甚小,柱撑膨润土的最佳吸附pH在6~8之间;膨润土的分配系数随着溶液中EDTA与Cu2 的摩尔比的增加而减少,当摩尔比>2后,分配系数趋于稳定;柱撑膨润土羟基吸附位的活性是决定吸附性能的关键因素;吸附过程符合Langmuir和Freundlich等温吸附模型,吸附容量的大小和吸附作用强弱的顺序为:羟基铁铝膨润土>羟基铁膨润土>天然膨润土. 相似文献
250.
变频控制DO下SBR硝化反应控制参数及节能的中试研究 总被引:2,自引:0,他引:2
根据微生物好氧反应的需氧量调节曝气量在当今能源紧缺的形势下具有十分重要的意义.为了研究曝气量大小对SBR实时控制参数pH、DO的影响,采用变频器调节曝气量以控制系统不同的DO浓度,以60 m3中试SBR反应器处理北京市北小河污水处理厂城市污水,考察了硝化过程中pH值、DO与有机物去除及硝化过程的相关性,并引入了新的控制参数--变频频率f.试验结果表明,控制溶解氧浓度较低时,pH值不能作为硝化结束的控制参数,但可根据变频频率f的特征点判断硝化反应的结束;控制溶解氧为3.0 mg/L和4.0 mg/L时,DO、pH值、变频频率f都可作为硝化结束的控制参数,同时,变频控制可有效降低单位时间内风机的能耗. 相似文献