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201.
Shortage in phosphorus (P) resources and P wastewater pollution is considered as a serious problem worldwide. The application of modified biochar for P recovery from wastewater and reuse of recovered P as agricultural fertilizer is a preferred process. This work aims to develop a calcium and magnesium loaded biochar (Ca-Mg/biochar) application for P recovery from biogas fermentation liquid. The physico-chemical characterization, adsorption efficiency, adsorption selectivity, and postsorption availability of Ca-Mg/biochar were investigated. The synthesized Ca-Mg/biochar was rich in organic functional groups and in CaO and MgO nanoparticles. With the increase in synthesis temperature, the yield decreased, C content increased, H content decreased, N content remained the same basically, and BET surface area increased. The P adsorption of Ca-Mg/biochar could be accelerated by nano-CaO and nano-MgO particles and reached equilibrium after 360 min. The process was endothermic, spontaneous, and showed an increase in the disorder of the solid-liquid interface. Moreover, it could be fitted by the Freundlich model. The maximum P adsorption amounts were 294.22, 315.33, and 326.63 mg/g. The P adsorption selectivity of Ca-Mg/biochar could not be significantly influenced by the typical pH level of biogas fermentation liquid. The nano-CaO and nano-MgO particles of Ca-Mg/biochar could reduce the negative interaction effects of coexisting ions. The P releasing amounts of postsorption Ca-Mg/biochar were in the order of Ca-Mg/B600 > Ca-Mg/B450 > Ca-Mg/B300. Results revealed that postsorption Ca-Mg/biochar can continually release P and is more suitable for an acid environment. 相似文献
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203.
Qian Zhao Hongjun Han Baolin Hou Haifeng Zhuang Shengyong Ji Fang Fang 《环境科学学报(英文版)》2014,26(11):2231-2239
A system combining granular activated carbon and powdered activated carbon technologies along with shortcut biological nitrogen removal (GAC-PACT-SBNR) was developed to enhance total nitrogen (TN) removal for anaerobically treated coal gasification wastewater with less need for external carbon resources. The TN removal efficiency in SBNR was significantly improved by introducing the effluent from the GAC process into SBNR during the anoxic stage, with removal percentage increasing from 43.8%49.6% to 68.8%-75.8%. However, the TN removal rate decreased with the progressive deterioration of GAC adsorption. After adding activated sludge to the GAG compartment, the granular carbon had a longer service-life and the demand for external carbon resources became lower. Eventually, the TN removal rate in SBNR was almost constant at approx. 43.3%, as compared to approx. 20.0% before seeding with sludge. In addition, the production of some alkalinity during the denitrification resulted in a net savings in alkalinity requirements for the nitrification reaction and refractory chemical oxygen demand (COD) degradation by autotrophic bacteria in SBNR under oxic conditions. PACT showed excellent resilience to increasing organic loadings. The microbial community analysis revealed that the PACT had a greater variety of bacterial taxons and the dominant species associated with the three compartments were in good agreement with the removal of typical pollutants. The study demonstrated that pre-adsorption by the GAC-sludge process could be a technically and economically feasible method to enhance TN removal in coal gasification wastewater (CGW). 相似文献
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三峡库区库中干流及支流水体夏季二氧化碳分压及扩散通量 总被引:16,自引:10,他引:6
以三峡库区库中干流以及主要支流——梅溪河为研究区,于2013年5月对该区域水体中溶解二氧化碳分压(pCO2)进行了走航观测.结果表明,夏季梅溪河表层pCO2为6.8~7.5 Pa,三峡库区库中长江干流表层pCO2为201.4~210.2 Pa.在库区干、支流交汇的过渡区水体剖面上,表层水体pCO2最低为53.5 Pa,随着水深增加,pCO2急剧增大,在3 m处达到约210Pa后基本保持不变.通过计算,库区支流梅溪河和库区干流表层水体的CO2释放通量分别为-7.48 mmol·(m2·d)-1和39.58 mmol·(m2·d)-1.结果表明,库区支流梅溪河表现为大气中CO2的"汇",而库区干流表现为CO2的"源",库区干、支流水体在CO2的释放上有显著差异. 相似文献
207.
采用还原-共沉淀法制备了无定型纳米复合Fe-Ti氧化物(FFT)吸附剂,并研究其对水中低浓度As(Ⅴ)的去除性能.XRD表征结果表明,制备的纳米FFT物相为无定型,BET比表面积达325.3 m2·g-1,计算得到的BJH吸附平均孔径为2.46 nm(4V/A),颗粒分布均匀.同时,考察了纳米FFT吸附As(Ⅴ)的动力学、热力学、吸附等温线,以及温度、水中共存离子对其去除As(Ⅴ)的影响.结果发现,纳米FFT对As(Ⅴ)的吸附符合拟二级动力学模型,计算出的孔道扩散系数DP在10-11~10-13cm2·s-1之间,显示孔扩散是速率限速步骤.Langmuir、Freundlich和DubininRadushkevich(D-R)吸附等温式均可较好地拟合吸附行为,低浓度下Langmuir吸附模型计算出的Qm达到26.46 mg·g-1.最后,研究了地下水中常见的共存离子对吸附的影响,发现Ca2+、Mg2+能够促进吸附,H2PO-4和HCO-3则明显抑制吸附过程. 相似文献
208.
A series of calcined carbonate layered double hydroxides (CLDHs) with various metal compositions and different M^2+/M^3+ ratios were prepared as adsorbents for perchlorate. Adsorption isotherms fit Langmuir model well, and the adsorption amount followed the order of MgA1-CLDHs 1〉 MgFeCLDHs 〉〉 ZnA1-CLDHs. The isotherms of MgA1-CLDHs and MgFe-CLDHs displayed a two-step shape at low and high concentration ranges and increased with an increase in the M^2+/M^3+ ratio from 2 to 4. The two-step isotherm was not observed for ZnA1-CLDHs, and the adsorption was minimally affected by the M^2+/M^3+ ratio. The LDHs, CLDHs and the reconstructed samples were characterized by X-ray diffraction, SEM, FT-IR and Raman spectra to delineate the analysis of perchlorate adsorption mechanisms. The perchlorate adsorption of MgA1-CLDHs and MgFe-CLDHs was dominated by the structural memory effect and the hydrogen bonds between the free hydroxyl groups on the reconstructed-LDHs and the oxygen atoms of the perchlorates. For ZnAI-CLDHs, the perchlorate adsorption was controlled by the structural memory effect only, as the hydroxyl groups on the hydroxide layers preferred to form strong hydrogen bonds with carbonate over perchlorate, which locked the intercalated perchlorate into a more confined nano-interlayer. Several distinct binding mechanisms of perchlorate by CLDHs with unique M^2+ ions were proposed. 相似文献
209.
Bo Yao Lingxi Zhou Lingjun Xi Gen Zhang Lifeng Guo Zhao Liu Shuangxi Fang 《环境科学学报(英文版)》2014,26(12):2451-2458
We present in-situ measurements of atmospheric sulfur hexafluoride(SF6) conducted by an automated gas chromatograph–electron capture detector system and a gas chromatography/mass spectrometry system at a regional background site, Shangdianzi,in China, from June 2009 to May 2011, using the System for Observation of Greenhouse gases in Europe and Asia and Advanced Global Atmospheric Gases Experiment(AGAGE)techniques. The mean background and polluted mixing ratios for SF6 during the study period were 7.22 × 10-12(mol/mol, hereinafter) and 8.66 × 10-12, respectively. The averaged SF6 background mixing ratios at Shangdianzi were consistent with those obtained at other AGAGE stations located at similar latitudes(Trinidad Head and Mace Head), but larger than AGAGE stations in the Southern Hemisphere(Cape Grim and Cape Matatula). SF6 background mixing ratios increased rapidly during our study period, with a positive growth rate at 0.30 × 10-12year-1. The peak to peak amplitude of the seasonal cycle for SF6 background conditions was 0.07 × 10-12, while the seasonal fluctuation of polluted conditions was 2.16 × 10-12. During the study period, peak values of SF6 mixing ratios occurred in autumn when local surface horizontal winds originated from W/WSW/SW/SWS/S sectors, while lower levels of SF6 mixing ratios appeared as winds originated from N/NNE/NE/ENE/E sectors. 相似文献
210.
固定化曝气生物滤池处理采油废水 总被引:11,自引:2,他引:9
采用一种特殊载体固定复合微生物B350M在曝气生物滤池反应系统中处理采油废水.废水中的盐度>0.5%,N、P营养缺乏,有机物浓度较低.在HRT为4h、COD容积负荷为1.07 kg/(m3·d)的条件下,小试反应装置稳定运行142d,处理效果良好,石油类、TOC、COD和H2S的平均降解效率分别达到90.5%、74.4%、85.6%和100%.GC-MS分析表明,进水中含有机物27种,其中烷烃类23种,芳烃类4种.此反应系统可以将大分子量烷烃类物质(C18H38至C28H58),尤其是其中的支链烷烃切碎形成小分子量物质,并有效地处理菲等多环芳烃.反应系统中,生态多样性丰富,载体为微生物提供了良好的水、气环境,抵御盐度、有机污染物的毒害作用,并可以固定丝状菌,因而避免出现污泥膨胀,出水SS过高等影响出水水质的情况. 相似文献