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41.
利用便携式车载排放测试系统(PEMS)对2辆加装氧化催化转化器(DOC)和催化型柴油颗粒捕集器(CDPF)与否的国III重型柴油货车进行实际道路排放测试.结果表明,2辆改造重型柴油车的CO、THC、固态颗粒物粒数(SPN)和黑碳(BC)实际道路排放因子分别为(1.31±0.37)g/(kW×h)、(0.20±0.03) g/(kW×h)、(7.13×1010±5.27×1010)个/(kW×h)和(0.69±0.06)mg/(kW×h),相对于原始排放(拆除DOC+CDPF)分别降低52.48%、55.69%、99.91%和99.22%.从低速、中速到高速,CO和THC减排比例呈现上升趋势,然而运行工况对SPN和BC减排比例则无显著影响.加装DOC+CDPF会导致NO2在NOx中的占比升高,且从低速、中速到高速涨幅依次增大,但对NOx无明显减排效益,其排放因子为9.53~9.83g/(kW×h),远高于实验室排放限值. 相似文献
42.
43.
反硝化生物阴极微生物燃料电池(MFC)以电极为电子供体,在自养条件下完成硝酸盐去除过程.本研究以碳布(CC)为基底材料,分别制备获得还原氧化石墨烯修饰(rGO-CC),聚苯胺修饰(PANI-CC)及二者复合修饰的CC电极(rGO/PANI-CC),并考察其作为阴极材料对反硝化生物阴极MFC产电脱氮性能的影响.扫描电镜结果显示,rGO-CC和PANI-CC的碳纤维分别被片层状rGO和网状PANI覆盖,而rGO/PANI-CC表面呈现PANI在附着rGO的碳纤维上团聚的形貌,均增大了碳布的比表面积.循环伏安测试显示,rGO/PANI-CC具有最高的电化学活性.以rGO-CC,PANI-CC和rGO/PANI-CC为阴极构建MFC的产电能力分别提高了82%,24%和41%,其阴极对NO3--N的去除能力增强了23%,9%和13%.16S rDNA测序结果揭示修饰后电极表面微生物的多样性下降,Stappia和Pacacoccus属微生物的丰度增加. 相似文献
44.
微塑料作为一种持久性污染物,对土壤生态系统具有严重影响,土壤中微塑料的污染已愈加受到国内外学者的广泛关注。当前关于土壤环境中微塑料的研究较少,针对当前土壤中微塑料的来源、分布、降解迁移、生态效应及污染防治等方面进行综述。主要包括以下几个方面:1)概括土壤生态系统中微塑料的来源、分布特点和迁移降解规律,确定了土壤环境中微塑料的赋存状态;2)总结土壤生态系统中微塑料与其他污染物的复合效应;3)分析了微塑料对土壤理化性质、动物、植物、微生物的影响,并揭示了微塑料对于土壤生态系统的影响;4)根据土壤微塑料的分布特点、降解迁移及生态效应提出污染防治措施。最后,对今后土壤微塑料的研究重点进行了展望。 相似文献
45.
The performance of Ce-OMS-2 catalysts was improved by tuning the fill percentage in the hydrothermal synthesis process to increase the oxygen vacancy density. The Ce-OMS-2 samples were prepared with different fill percentages by means of a hydrothermal approach (i.e. 80%, 70%, 50% and 30%). Ce-OMS-2 with 80% fill percentage (Ce-OMS-2-80%) showed ozone conversion of 97%, and a lifetime experiment carried out for more than 20?days showed that the activity of the catalyst still remained satisfactorily high (91%). For Ce-OMS-2-80%, Mn ions in the framework as well as K ions in the tunnel sites were replaced by Ce4+, while for the others only Mn ions were replaced. O2-TPD and H2-TPR measurements proved that the Ce-OMS-2-80% catalyst possessed the greatest number of mobile surface oxygen species. XPS and XAFS showed that increasing the fill percentage can reduce the AOS of Mn and augment the amount of oxygen vacancies. The active sites, which accelerate the elimination of O3, can be enriched by increasing the oxygen vacancies. These findings indicate that increasing ozone removal can be achieved by tuning the fill percentage in the hydrothermal synthesis process. 相似文献
46.
F-V_2 O_5-WO3/Ti02 catalysts were prepared by the impregnation method.As the content of F ions increased from 0.00 to 0.35 wt.%,the NO conversion of F-V_2 O_5-WO_3/TiO_2 catalysts initially increased and then decreased.The 0.2 F-V_2 O_5-WO_3/TiO_2 catalyst(0.2 wt.% F ion)exhibited the best denitration(De-NOx) performance,with more than 95% NO conversion in the temperature range 160-360℃,and 99.0% N2 selectivity between 110 and 280℃.The addition of an appropriate amount of F ions eroded the surface morphology of the catalyst and reduced its grain size,thus enhancing the NO conversion at low temperature as well as the sulfur and water resistance of the V_2 O_5-WO3/Ti02 catalyst.After selective catalytic reduction(SCR) reaction in a gas flow containing SO_2 and H_2 O,the number of NH3 adsorption sites,active component content,specific surface area and pore volume decreased to different degrees.Ammonium sulfate species deposited on the catalyst surface,which blocked part of the active sites and reduced the NO conversion performance of the catalyst.On-line thermal regeneration could not completely recover the catalyst activity,although it prolonged the cumulative life of the catalyst.In addition,a mechanism for the effects of S02 and H_2 O on catalyst NO conversion was proposed. 相似文献
47.
Ozone (O3), as a harmful air pollutant, has been of wide concern. Safe, efficient, and economical O3 removal methods urgently need to be developed. Catalytic decomposition is the most promising method for O3 removal, especially at room temperature or even subzero temperatures. Great efforts have been made to develop high-efficiency catalysts for O3 decomposition that can operate at low temperatures, high space velocity and high humidity. First, this review describes the general reaction mechanism of O3 decomposition on noble metal and transition metal oxide catalysts. Then, progress on the O3 decomposition performance of various catalysts in the past 30 years is summarized in detail. The main focus is the O3 decomposition performance of manganese oxides, which are divided into supported manganese oxides and non-supported manganese oxides. Methods to improve the activity, stability, and humidity resistance of manganese oxide catalysts for O3 decomposition are also summarized. The deactivation mechanisms of manganese oxides under dry and humid conditions are discussed. The O3 decomposition performance of monolithic catalysts is also summarized from the perspective of industrial applications. Finally, the future development directions and prospects of O3 catalytic decomposition technology are put forward. 相似文献
48.
In this work,we fabricated three kinds of Ag/Fe_2O_3 model catalysts with different morphologies to study the interfacial interactions between Ag and Fe_2O_3,and how they affected the catalytic activity in hydrogenation of p-nitrophenol was explored.The hydrothermal method was used to synthesize the metal oxide supported silver catalyst,with various morphologies including nanoplates(NPs),nanospheres(NSs),and nanocubes(NCs).The crystal structure,morphology and surface elements of the composite were investigated by various measurements,such as X-ray diffraction(XRD),scanning electron microscopy(SEM),transmission electron microscopy(TEM) and X-ray photoelectron spectroscopy(XPS).The catalytic activity was also evaluated by the reduction of p-nitrophenol to p-aminophenol.It was found that the activities of the above catalysts varied with the morphology of the support.Among them,Ag/Fe_2O_3 NPs promoted the highest performance,Ag/Fe_2O_3 NSs were slightly inferior,and Ag/Fe_2O_3 NCs were the worst.At last,we ascribed the remarkable activity of Ag/Fe_2O_3 NPs to the strong metal-support interactions between Ag and Fe_2O_3. 相似文献
49.
Biogenic volatile organic compounds (BVOCs) in the atmosphere play important roles in the formation of ground-level ozone and secondary organic aerosol (SOA) in global scale and also in regional scale under some condition due to their large amount and relatively higher reactivity. In places with high plant cover in the tropics and in China where air pollution is serious, the effect of BVOCs on ozone and secondary organic aerosols is strong. The present research aims to provide a comprehensive review about the emission rate, emission inventory, research methods, the influencing factors of BVOCs emissions, as well as their impacts on atmospheric environment quality and human health in recent years in Asia based on the summary and analysis of literatures. It is suggested to use field direct measurement method to obtain the emission rate and model method to calculate the emission amount. Several recommendations are given for future investigation and policy development on BVOCs emission. 相似文献
50.
为了解深圳市龙岗区大气颗粒物中多溴联苯醚的污染状况,于2017年1月、4月、8月和11月分别采集龙岗区大气颗粒物样品.利用气相色谱-质谱联用仪(GC/MS)对深圳市龙岗区4个功能区(工业区、商业区、居民区和生态区)的80个大气颗粒物样品进行检测,得到PBDEs(多溴联苯醚)8种单体(BDE-28、BDE-47、BDE-99、BDE-100、BDE-153、BDE-154、BDE-183、BDE-209)的质量浓度,同时研究了大气颗粒物中PBDEs质量浓度的时空分布特征.结果表明:①深圳市龙岗区大气颗粒物中ρ(∑8PBDEs)(∑8PBDEs为PBDEs 8种单体的加和)范围为0.07~77.80 pg/m3,ρ(∑8PBDEs)年均值为(6.86±14.17)pg/m3.ρ(BDE-209)范围为0.01~76.23 pg/m3,年均值为(5.10±13.58)pg/m3,BDE-209为主要污染单体.② 4个功能区的ρ(∑8PBDEs)平均值大小顺序依次为工业区(13.65 pg/m3)>商业区(7.75 pg/m3)>生态区(3.95 pg/m3)>居民区(2.19 pg/m3),工业区是环境空气颗粒物中PBDEs的主要污染区.③ ρ(∑8PBDEs)平均值的季节性变化规律为春季(13.32 pg/m3)>冬季(9.18 pg/m3)>秋季(2.17 pg/m3)>夏季(1.51 pg/m3),符合深圳市亚热带海洋季风气温和气候对环境空气中颗粒物质量浓度的影响规律.研究显示,深圳市龙岗区大气颗粒物中PBDEs质量浓度处于较高水平,污染严重,建议减少含PBDEs产品的生产、使用和运输等活动,或找到更利于环境安全和人体健康的替代品,降低PBDEs对该地区的污染. 相似文献