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41.
为了研究地下水中阴离子对载镁活化天然沸石除氟效果的影响,考察了4种主要阴离子——Cl-,HCO3-,SO42-,PO43-的影响,并分析了吸附剂的除氟机理及表面结构和成分。结果表明:对于初始氟浓度不同的水样,随着阴离子浓度的增加,吸附剂对氟的去除效率逐渐降低。Cl-对吸附剂除氟效果影响较小,氟去除率降低较慢;随着HCO3-浓度的增大(由100 mg/L到1 000 mg/L),水样pH缓慢由7.48增大到9.44,而氟去除率则由63.78%缓慢下降到52.70%(2 mg/L);SO42-及PO43-对改性沸石除氟效果影响较大,氟去除率降低较快,且SO42-的影响大于PO43-。所以,镁改性天然沸石对该4种阴离子的吸附顺序是:SO42->PO43->HCO3->Cl-。 相似文献
42.
采用陶粒滤料曝气生物滤池(BAF)处理邻苯二甲酸丁基苄酯(BBP)模拟废水,考察了空床接触时间(EBCT)、温度对BBP的去除效果的影响;运用气质联用仪(GC-MS)分析了BBP在曝气生物滤池内降解的中间产物并推测其可能的降解途径。结果表明,当温度为25℃,空床接触时间(EBCT)为8 h时,BAF对BBP的降解效果良好,去除率达到95.7%;BAF对BBP的去除率随着温度的升高和EBCT的增加而增大,EBCT为去除效果的主要影响因素。BAF出水中检测到邻苯二甲酸二丁酯(DBP)、邻苯二甲酸二甲酯(DMP)以及邻苯二甲酸(PA)等降解产物,据此推测邻苯二甲酸丁基苄酯的生物降解途径可能为BBP的苯环先断裂生成邻苯二甲酸二丁酯,而后断裂一个酯键形成单酯,接着再断裂另一酯键形成邻苯二甲酸,最终分解成二氧化碳和水。 相似文献
43.
天然藻类吸附重金属的研究 总被引:1,自引:0,他引:1
传统的重金属废水处理技术存在耗能高、运行成本高及存在二次污染的问题等诸多劣势;而天然海藻由于其来源广、产量大,在处理重金属废水方面存在较多的优点。介绍了藻类处理重金属离子的研究背景、现状,阐述了藻类处理重金属的优点、机理,重点介绍了海藻处理废水过程中的各种影响因素,并对海藻处理废水的应用前景进行了展望。 相似文献
44.
水体中苯胺光降解的实验研究 总被引:1,自引:0,他引:1
为了更好地了解苯胺类物质在环境中的化学行为,在自行设计的光化学反应器上进行模拟天然水体的苯胺光降解实验,用气相色谱法测定苯胺的残余质量浓度,考察了水体pH值、光强、反应时间、光敏化剂、水质等条件影响下苯胺的光降解效果和规律.3h内苯胺在3个不同体系中的降解效果从大到小依次是:去离子水模拟天然水体、加入光敏化物质的灭菌河水、未加光敏化物质的灭菌河水.pH值为5.0,Fe2 、过氧化氢、腐殖质存在时苯胺的光降解效果较好. 相似文献
45.
Shiping Zhou Changqun Duan Wong Hang Gi Michelle Fazhong Yang Xuehua Wang 《环境科学学报(英文版)》2011,23(4):676-680
Toxicities were assessed for a pyrethroid (cypermethrin) and an organophosphate insecticide (chlorpyrifos) individually and in
combination. A series of tests were conducted on di erent responses (acute, chronic, behavioral) of earthworms of species Eisenia
fetida andrei in the ecological risk assessment of these pesticides. The results showed that the toxicity of the mixture of cypermethrin
and chlorpyrifos was significantly higher than either of these pesticides individually, especially on the earthworm’s chronic responses.
At a concentration of 5 mg/kg, the mixture caused significant reductions on the growth and reproduction rates of earthworms, but did
not cause any significant e ect when the individual was tested. The increase in toxicity of the pesticide mixture means that the use of
toxicity data obtained exclusively from single-pesticide experiments may underestimate the ecological risk of pesticides that actually
present in the field. 相似文献
46.
Meeta Lavani Priyangshu M. Sarm Ajoy K. Man Simrita Cheem Banwari La 《环境科学学报(英文版)》2011,23(8):1394-1402
We compared the efficacy of a natural biocide with four chemical tetrakishydroxymethyl phosphonium sulfonate, benzyl trimethyl
ammonium chloride, and formaldehyde, glutaraldehyde, to control microbial induced corrosion in oil pipelines. The efficacy of biocides
were monitored against Desulfovibrio vulgaris and Desulfovibrio gigas in experimental pipes by measuring cell counts, H2S production,
Fe(II) production, production of extracellular polymeric substances and structure of biofilm. The treatment with cow urine had minimum
planktonic cell counts of 3 102 CFU/mL as well as biofilm cell counts of 9 101 CFU/mL as compared with tetrakishydroxyl methyl
phosphonium sulfonate, benzyl trimethyl ammonium chloride, formaldehyde and glutaraldehyde. Sulfide production was the lowest
with cow urine (0.08 mmol/L), followed by tetrakishydroxymethyl phosphonium sulfonate 0.72 mmol/L. On day 90 of treatment,
Fe(II) production was also found to be the lowest with cow urine. The scanning electron microscopic studies indicated that the biofilm
bacteria were killed by cow urine. These results demonstrate the cow urine mediated control of microbially induced corrosion, and this
is indicative of its potential as a viable substitute of toxic biocides. To the best of our knowledge, this seems to be the first report which
screens possible biocidal activity by cow urine as compared to the most common biocides which oil industry is currently using. 相似文献
47.
48.
Xiuying Zhao Xinming Wang Xiang Ding Quanfu He Zhou Zhang Tengyu Liu Xiaoxin Fu Bo Gao Yunpeng Wang Yanli Zhang Xuejiao Deng Dui Wu 《环境科学学报(英文版)》2014,26(1):110-121
Organic acids as important constituents of organic aerosols not only influence the aerosols' hygroscopic property, but also enhance the formation of new particles and secondary organic aerosols. This study reported organic acids including C14–C32fatty acids, C4–C9dicarboxylic acids and aromatic acids in PM2.5collected during winter 2009 at six typical urban, suburban and rural sites in the Pearl River Delta region. Averaged concentrations of C14–C32fatty acids, aromatic acids and C4– C9 dicarboxylic acids were 157, 72.5 and 50.7 ng/m3, respectively. They totally accounted for 1.7% of measured organic carbon. C20–C32fatty acids mainly deriving from higher plant wax showed the highest concentration at the upwind rural site with more vegetation around, while C14–C18fatty acids were more abundant at urban and suburban sites, and dicarboxylic acids and aromatic acids except 1,4-phthalic acid peaked at the downwind rural site. Succinic and azelaic acid were the most abundant among C4–C9dicarboxylic acids, and 1,2-phthalic and 1,4-phthalic acid were dominant aromatic acids. Dicarboxylic acids and aromatic acids exhibited significant mutual correlations except for 1,4-phthalic acid, which was probably primarily emitted from combustion of solid wastes containing polyethylene terephthalate plastics. Spatial patterns and correlations with typical source tracers suggested that C14–C32fatty acids were mainly primary while dicarboxylic and aromatic acids were largely secondary. Principal component analysis resolved six sources including biomass burning, natural higher plant wax, two mixed anthropogenic and two secondary sources; further multiple linear regression revealed their contributions to individual organic acids. It turned out that more than 70% of C14–C18fatty acids were attributed to anthropogenic sources, about 50%–85% of the C20–C32fatty acids were attributed to natural sources, 80%–95% of dicarboxylic acids and 1,2-phthalic acid were secondary in contrast with that 81% of 1,4-phthalic acid was primary. 相似文献
49.
50.
为研究淹水条件下光照对土-水界面磷释放的影响,以三峡库区消落带典型土壤为对象,通过室内自然光照试验,讨论了铁还原及有机质降解对磷释放的影响,分析光照对淹水土壤磷释放的影响机制.结果表明,光照对淹水土壤磷释放存在一定程度的抑制作用,光照作用下淹水紫色潮土上覆水体中TP浓度范围为0.018~0.033 mg·L-1,避光处理为0.02~0.057mg·L-1,灰棕紫泥光照下TP浓度范围为0.028~0.045 mg·L-1,避光处理为0.04~0.084 mg·L-1.光照引起淹水土壤中铁氧化物的变化可能是光照抑制磷释放的重要原因.光照导致土壤中铁氧化物饱和程度降低,铁还原和无定形铁生成受阻进一步加深了光照对磷释放的抑制影响.CO2和CH4反映淹水土壤有机质分解情况,光照降低有机碳的转化效率,加速土壤中无机电子受体的消耗,解释了光照作用下铁氧化物的变化.由此可见,光照对淹水土壤磷释放的抑制与淹水土壤中铁还原和有机质分解密切相关. 相似文献