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211.
经过对PH玻璃电极对比观测实验,总结其在日常观测中衰减变化规律,以及PH电极失效前所具有的特征;讨论了对现有PH观测数据进行修正的方法,并编著相关修正程序;分析日常存在的测量误差,提出提高观测精度的措施。 相似文献
212.
讨论了城市污水经过A/O工艺处理时活性污泥的二次污染问题。将原水、处理后的出水及活性污泥用甲苯萃取,萃取相经过真空浓缩后,采用GC/MS测定了样品中的有机化合物,结果表明,在A/O工艺处理城市污水过程中,活性污泥的吸附作用是主要的,降解作用是次要的;A/O工艺所排放的活性污泥仍然是一种危险的污染物。 相似文献
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214.
Manganese uptake and accumulation by the hyperaccumulator plant Phytolacca acinosa Roxb. (Phytolaccaceae) 总被引:9,自引:0,他引:9
Xue SG Chen YX Reeves RD Baker AJ Lin Q Fernando DR 《Environmental pollution (Barking, Essex : 1987)》2004,131(3):393-399
The perennial herb Phytolacca acinosa Roxb. (Phytolaccaceae), which occurs in Southern China, has been found to be a new manganese hyperaccumulator by means of field surveys on Mn-rich soils and by glasshouse experiments. This species not only has remarkable tolerance to Mn but also has extraordinary uptake and accumulation capacity for this element. The maximum Mn concentration in the leaf dry matter was 19,300 microg/g on Xiangtan Mn tailings wastelands, with a mean of 14,480 microg/g. Under nutrient solution culture conditions, P. acinosa could grow normally with Mn supplied at a concentration of 8000 micromol/l, although with less biomass than in control samples supplied with Mn at 5 micromol/l. Manganese concentration in the shoots increased with increasing external Mn levels, but the total mass of Mn accumulated in the shoots first increased and then decreased. At an Mn concentration of 5000 micromol/l in the culture solution, the Mn accumulation in the shoot dry matter was highest (258 mg/plant). However, the Mn concentration in the leaves reached its highest value (36,380 microg/g) at an Mn supply level of 12,000 micromol/l. These results confirm that P. acinosa is an Mn hyperaccumulator which grows rapidly, has substantial biomass, wide distribution and a broad ecological amplitude. This species provides a new plant resource for exploring the mechanism of Mn hyperaccumulation, and has potential for use in the phytoremediation of Mn-contaminated soils. 相似文献
215.
改进的硫酸盐-聚乙烯醇法包埋藻菌脱氮除磷研究 总被引:1,自引:0,他引:1
采用改进的硫酸盐-PVA固定化法将藻与菌混合固定。在三种不同藻菌比的情况下,固定化系统对氮去除均可达100%,但是去除速度与固定的细菌量有关,细菌量越大,对氮的去除速度越快;对磷的去除随实验进行,最大去除率逐步下降,其下降速度与固定藻的量有关,藻量越大,下降速度越慢。由此说明脱氮的主要贡献者是细菌,而藻对除磷起了主要作用。为达到有效的脱氮除磷,应适当提高固定化藻的浓度,藻菌比应大于2:1。透射电镜照片显示,在聚乙烯醇载体上,藻类的生长没有受到限制。 相似文献
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217.
Lee K Parkhurst WJ Xue J Ozkaynak AH Neuberg D Spengler JD 《Journal of the Air & Waste Management Association (1995)》2004,54(3):352-359
An ozone (O3) exposure study was conducted in Nashville, TN, using passive O3 samplers to measure six weekly outdoor, indoor, and personal O3 exposure estimates for a group of 10- to 12-yr-old elementary school children. Thirty-six children from two Nashville area communities (Inglewood and Hendersonville) participated in the O3 sampling program, and 99 children provided additional time-activity information by telephone interview. By design, this study coincided with the 1994 Nashville/Middle Tennessee Ozone Study conducted by the Southern Oxidants Study, which provided enhanced continuous ambient O3 monitoring across the Nashville area. Passive sampling estimated weekly average outdoor O3 concentrations from 0.011 to 0.O30 ppm in the urban Inglewood community and from 0.015 to 0.042 ppm in suburban Hendersonville. The maximum 1- and 8-hr ambient concentrations encountered at the Hendersonville continuous monitor exceeded the levels of the 1- and 8-hr metrics for the O3 National Ambient Air Quality Standard. Weekly average personal O3 exposures ranged from 0.0013 to 0.0064 ppm (7-31% of outdoor levels). Personal O3 exposures reflected the proportional amount of time spent in indoor and outdoor environments. Air-conditioned homes displayed very low indoor O3 concentrations, and homes using open windows and fans for ventilation displayed much higher concentrations. 相似文献
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219.
四氯化碳的生产和使用,给人类带来了较大危害。为此,采用纳米铁粉这一新方法对其进行脱氯处理。试验以纳米级铁粉对四氯化碳的脱氯率为考察指标,选用L25(5^6)正交试验方案,考察了降解介质的初始pH值、纳米铁粉的质量、降解温度、摇床转速和脱氯时间5个影响因素。结果表明,pH值这一因素有极显著影响;在得出的纳米铁粉对四氯化碳脱氯的最佳工艺条件下,获得了99.5%的脱氯率,为有机氯化物脱氯开辟了一条新途径。 相似文献
220.
Runmiao Xue Ariel Donovan Haiting Zhang Yinfa M Craig Adams John Yang Bin Hu Enos Inniss Todd Eichholz Honglan Shi 《环境科学学报(英文版)》2018,30(2):82-91
When adding sufficient chlorine to achieve breakpoint chlorination to source water containing high concentration of ammonia during drinking water treatment, high concentrations of disinfection by-products(DBPs) may form. If N-nitrosamine precursors are present, highly toxic N-nitrosamines, primarily N-nitrosodimethylamine(NDMA), may also form. Removing their precursors before disinfection should be a more effective way to minimize these DBPs formation. In this study, zeolites and activated carbon were examined for ammonia and N-nitrosamine precursor removal when incorporated into drinking water treatment processes.The test results indicate that Mordenite zeolite can remove ammonia and five of seven N-nitrosamine precursors efficiently by single step adsorption test. The practical applicability was evaluated by simulation of typical drinking water treatment processes using six-gang stirring system. The Mordenite zeolite was applied at the steps of lime softening, alum coagulation, and alum coagulation with powdered activated carbon(PAC) sorption. While the lime softening process resulted in poor zeolite performance, alum coagulation did not impact ammonia and N-nitrosamine precursor removal. During alum coagulation, more than67% ammonia and 70%–100% N-nitrosamine precursors were removed by Mordenite zeolite(except 3-(dimethylaminomethyl)indole(DMAI) and 4-dimethylaminoantipyrine(DMAP)). PAC effectively removed DMAI and DMAP when added during alum coagulation. A combination of the zeolite and PAC selected efficiently removed ammonia and all tested seven N-nitrosamine precursors(dimethylamine(DMA), ethylmethylamine(EMA), diethylamine(DEA), dipropylamine(DPA), trimethylamine(TMA), DMAP, and DMAI) during the alum coagulation process. 相似文献