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161.
燃煤烟气中的SO2和NOx是大气中重要的污染物,开发高效、经济的同步脱硫脱硝技术是环保领域的研究热点。针对现有同步脱硫脱硝技术存在的氧化剂成本较高和产物不能资源化利用等突出问题,提出了软锰矿浆烟气同步脱硫脱硝,并副产硫酸锰和硝酸锰的资源化新工艺。研究结果表明:软锰矿浆可以有效的脱除烟气中的SO2和NOx,反应产物分别为硫酸锰和硝酸锰。在烟道中注入臭氧,将难溶于水的NO快速氧化为NO2,可大大提高脱硝效率,在O3/NO=1.2的条件下可以达到72%的脱硝率、90%的脱硫率和85%的锰浸出率;吸收液经过空气氧化除铁和加入铜试剂除重金属后,结晶分离溶液得到的硫酸锰和硝酸锰可分别达到HG/T 2962—1999标准的硫酸锰产品和HG/T 3817—2006标准的工业硝酸锰产品要求。该工艺实现了SO2和NOx污染治理与低品位软锰矿资源化利用的双重目的,为SO2和NOx的资源化污染治理技术的开发和应用提供了新的思路。 相似文献
162.
蛭石吸附及解吸锌离子特性研究 总被引:2,自引:0,他引:2
用蛭石对锌离子的吸附解吸进行了实验研究,初步探讨了其对锌离子吸附解吸的机理。研究结果表明:蛭石对Zn^2+具有较强的吸附能力,吸附在8h左右接近平衡。随着锌离子浓度的增加,蛭石的吸附量也在逐渐增加,当锌离子浓度达到400mg/L时,吸附量趋于平稳。在完成吸附实验的基础上,分别采用过滤和取上清液的方法解吸,实验证明静置平衡后,取出上清液50ml,再加入50ml解吸剂的方法解吸效果较好;解吸时间在0h到12h,蛭石的解吸量呈现递增的趋势,且达到1.070mg/g;在12h到48h内,解吸量基本没有增加,其中在24h时达到最大解吸量1.074mg/g。不同的解吸剂对蛭石解吸锌离子影响效果不同:蒸馏水不能使锌离子解吸;K^+的影响作用相对于Na^+更明显,随着两种阳离子浓度的增加,蛭石的解吸量逐渐增加。 相似文献
163.
IntroductionClomazone,(2 [(2 chlorophenyl)methyl ] 4 ,4 dimethyl 3 isoxazolidinone) ,isasoil appliedisoxazolidinoneherbicideproducedbyFMCCorp .Itisintroducedforannualgrassandbroad spectrumweedsinsoybeans(Rani,1998;Vyas,2 0 0 0 ) .Itisalsocurrentlyregis… 相似文献
164.
This paper presented the characteristics of nitrogen and phosphorus pollution in Beijing surface water during the survey. A significant difference was found out in concentration distribution of various parameters of nitrogen and phosphorus. Most water bodies in five water systems were polluted by total nitrogen with the content even up to 120 mg/L which was higher than exceeded the fifth class standard of national surface water quality standard GB3838-2002 except for several segments of Chaobaihe and Yongdinghe. Ammonia and phosphorus showed a similar tendency of distribution with higher content in Daqinghe, Beiyunhe and Jiyunhe water systems, but with relatively low concentrations in Chaobaihe and Yongdinghe water systems. Meanwhile, nitrate was found at comparatively low content (mostly less than 10 mg/L) and could fit for corresponding water quality requirements. Totally, the water quality of Daqinghe, Jiyunhe and Beiyunhe river systems as well as the lower reaches of Yongdinghe and Chaobaihe was contaminated seriously with high content of total nitrogen and phosphorus. Through multivariate statistical approaches, it can be concluded that total nitrogen, ammonia and total phosphorus was highly correlated to chemical oxygen demand, biochemical oxygen demand, dissolved oxygen and electrical conductivity,which explained the same pollution source from anthropogenic activities. 相似文献
165.
IntroductionThemaintenanceofsoilfertilitydependsonthesizeandtheactivityofthesoilmicrobialbiomasswhichisoffundamentalimportanceinbiologicalcyclesofalmostallmajorplantnutrients(Robert,1992 ) .Thereisconsiderableinterestinstudyofsoilbiochemicalcharacteristic… 相似文献
166.
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168.
光电化学法处理水体中腐殖酸的初步研究 总被引:10,自引:3,他引:10
结合90年代欧美学者提出了高级化学氧化过程(Advancedchemicaloxidationprocess,AOP)原理,提出了并建立了一套光电化学联用的新用于处理难以生物降解的腐殖酸废水,实验表明,在通电1h加光条件下(I=0.2A)总有碳(TOC)去除率达到90%,色度去除率达到95%。 相似文献
169.
Removal of polycyclic aromatic hydrocarbons (PAHs) from different soil fractions of contaminated soil was investigated by using activated persulfate oxidation remediation in our research. The results showed that the light fraction, which accounted for only 10% of the soil, contained 30% of the PAHs at a concentration of 4352?mg/kg. The heavy fraction contained more high-molecular-weight PAHs, and the total PAH concentration was 625?mg/kg. After being oxidized, the removal rate of PAHs was 39% in the light fraction and nearly 90% in the heavy fraction. Among the different fractions of the heavy fraction, humic acid contained the highest concentration of PAHs, and consequently, the highest removal efficiency of PAHs was also in humic acid. Compared with the light fraction, the heavy fraction has more aromatic compounds and those compounds were broken down during the oxidation process, which may be the removal mechanism involved in the oxidation of high-ring PAHs. Similarly, the enhancement of C = C bonds after oxidation can also explain the poor removal of high-ring PAHs in the light fraction. These results imply that different fractions of soil vary in composition and structure, leading to differences in the distribution and oxidation efficiencies of PAHs. 相似文献
170.