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51.
建立了电感耦合等离子体原子发射光谱(ICP-AES)法测定磷生铁中3种元素Mn、P、Si的定量分析方法.通过试验选择257.610nm、185.942nm、212.412nm分别作为Mn、P、Si的分析谱线,无需进行光谱干扰校正.实验结果表明,各元素分析谱线线性相关系数大于0.9990.方法用于高磷铸铁标准物质分析,测定值与认定值相符,测定结果的相对标准偏差在0.21% (Mn) ~1.8% (P)范围. 相似文献
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54.
研究了两种不同形态MnO2(δ-MnO2和胶体MnO2)对难降解有机药物卡马西平(carbamazepine,CBZ)的去除效果,并通过液相色谱质谱联用技术(LC/MS)分析了不同pH值条件下δ-MnO2和胶体MnO2氧化转化CBZ的产物,探究其氧化转化途径.结果表明,δ-MnO2和胶体MnO2能通过化学氧化作用在2h内去除约1mg/L CBZ,相比之下,胶体MnO2受pH影响较小且单位质量Mn对CBZ具有更好的去除效果.δ-MnO2和胶体MnO2与CBZ反应过程中各检出7种和4种产物.胶体MnO2具有更强的氧化能力,越过了多种中间产物的产生步骤,使CBZ的降解途径更加简明. 相似文献
55.
O3 decomposition catalysts with excellent performance still need to be developed. In this study, Ag-modified manganese oxides (AgMnOx) were synthesized by a simple co-precipitation method. The effect of calcination temperature on the activity of MnOx and AgMnOx catalysts was investigated. The effect of the amount of Ag addition on the activity and structure of the catalysts was further studied by activity testing and characterization by a variety of techniques. The activity of 8%AgMnOx for ozone decomposition was significantly enhanced due to the formation of the Ag1.8Mn8O16 structure, indicating that this phase has excellent performance for ozone decomposition. The weight content of Ag1.8Mn8O16 in the 8%AgMnOx catalyst was only about 33.76%, which further indicates the excellent performance of the Ag1.8Mn8O16 phase for ozone decomposition. The H2 temperature programmed reduction (H2-TPR) results indicated that the reducibility of the catalysts increased due to the formation of the Ag1.8Mn8O16 structure. This study provides guidance for a follow-up study on Ag-modified manganese oxide catalysts for ozone decomposition. 相似文献
56.
This paper identifies newer areas of arsenic contamination in the District Kanker, which adjoins the District Rajnandgaon where high contamination has been reported earlier. A correlation with the mobile phase episodes of arsenic contamination has been identified, which further hinges on the complex geology of the area. Arsenic concentrations in both surface and groundwater, aquatic organisms (snail and water weeds) soil and vegetation of Kanker district and its adjoining area have been reported here. The region has been found to contain an elevated level of arsenic. All segments of the ecoysystem are contaminated with arsenic at varying degrees. The levels of arsenic vary constantly depending on the season and location. An analysis of groundwater from 89 locations in the Kanker district has shown high values of arsenic, iron and manganese (mean: 144, 914 and 371 μg L−1, respectively). The surface water of the region shows elevated levels of arsenic, which is influenced by the geological mineralised zonation. The most prevalent species in the groundwater is As(III), whereas the surface water of the rivers shows a significant contamination with the As(V) species. The analysis shows a bio-concentration of the toxic metals arsenic, nickel, copper and chromium. Higher arsenic concentrations (groundwater concentrations greater than 50 μg L−1) are associated with sedimentary deposits derived from volcanic rocks, hence mineral leaching appears to be the source of arsenic contamination. Higher levels of arsenic and manganese in the Kanker district have been found to cause impacts on the flora and fauna. A case study of episodic arsenical diarrhoea is presented. 相似文献
57.
Arthrobacter chlorophenolicus MN1409是1株分离自锰矿样品的高效锰氧化细菌。为了建立该菌株氧化Mn2+的适宜条件,研究了接种量、装液量、摇床转速、温度、pH值、Fe2+初始质量浓度和Mn2+初始质量浓度等理化因素对其锰氧化效率的影响。结果表明,接种量、装液量、转速和Mn2+初始质量浓度在一定范围内变化对锰氧化率影响不大;而温度、pH值和Fe2+初始质量浓度变化对锰氧化率有较大影响。当接种量为4%,装液量为60 mL,温度为25℃,摇床转速为100r/min,pH值为7,且有一定的Fe2+存在时,Arthrobacter chlorophenolicusMN1409对锰的氧化效率最高。 相似文献
58.
Manganese oxides (MnOx) have been demonstrated to be effective materials to activate Oxone (i.e., PMS) to degrade various contaminants. However, the contribution of direct oxidation by MnOx to the total contaminant degradation under acidic conditions was often neglected in the published work, which has resulted in different and even conflicting interpretations of the reaction mechanisms. Here, the role of MnOx (as both oxidants and catalysts) in the activation of Oxone was briefly discussed. The findings offered new insights into the reaction mechanisms in PMS-MnOx and provided a more accurate approach to examine contaminant degradation for water/wastewater treatment. 相似文献
59.
土壤中氧化铁的有机还原溶解动力学 总被引:1,自引:0,他引:1
研究了土壤中的氧化铁被两种酚化合物还原而溶解的动力学,结果表明,在pH恒定和有机还原剂过量的情况下,氧化铁的还原溶解符合一级反应动力学方程,还原溶解速率大小与土壤中氧化铁的结晶形态有关.氧化锰的存在影响着氧化铁的还原溶解,在存在足够的还原剂的条件下,两者可同时还原.实验中求得黄壤和赤红壤中氧化铁的还原溶解反应对[H+]的反应级数分别为0.126和0.174。土壤中氧化铁的还原溶解是一个受表面反应控制的过程,反应的速率控制步骤是表面的电子转移反应,磷酸根在土壤中的吸附占据了氧化铁表面的反应位,因而明显抑制还原溶解反应. 相似文献
60.
本文讨论了沉淀法和空气提气法去除电解锰废水中含有的锰(Mn~(2+))和氨-氮(NH_3-N),并研究了该方法的最佳条件,为废水日排放量在300—400T之间的工厂设计了废水处理路线。结果表明,上述方法处理后的废水中Mn~(2+)和NH_3-N含量达到或低于国家污水排放标准。 相似文献