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91.
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   
92.
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   
93.
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   
94.
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   
95.
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   
96.
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   
97.
余嘉政 《环境化学》1992,11(1):35-38
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   
98.
赵玲  彭平安  黄伟林 《生态环境》2005,14(2):195-198
研究了在二氧化锰催化引起的五氯酚的转化反应中,腐殖质前身化合物的加入对五氯酚去除率的影响,并以p-coumaricacid为代表研究了体系pH值、反应时间、二氧化锰的质量浓度以及腐殖质前生物的浓度和分子结构对去除率的影响。结果表明,反应的最佳pH值范围是4~4.70,去除率在80%左右。五氯酚在24h内去除速率较快,去除率达到75%左右;反应到168h,去除速率趋于0,去除率达到80%左右。相同条件下,无p-coumaricacid的对照体系中,对应的反应时间内去除率仅分别为20%和25%左右。五氯酚的去除率还随二氧化锰质量浓度和p-coumaricacid浓度的增加而增大。当二氧化锰的质量浓度由0增加到100g·L-1时,去除率由0增大为95%;而当p-coumaricacid的浓度由0增加到1mmol·L-1时,去除率由25%增大到100%左右。此外,不同腐殖质前身物的分子结构和浓度对去除率分别起到了提高、不明显改变和降低的作用。  相似文献   
99.
通过在本课题组自行设计的中空水冷转式垃圾焚烧炉上的实验研究,论文从工艺流程和NOx生成特性方面探讨了该新型焚烧炉的稳定燃烧和低污染排放技术特点;并与固定床焚烧炉作了实验研究比较,可知中空水冷转式垃圾焚烧炉在降低NOx浓度与提高燃尽率方面具有良好的性能。  相似文献   
100.
We studied the removal of nitrogen oxides pollutants via TiO2 Degussa P25 powder by photocatalysis. Parameters such as mass of catalyst, geometric irradiated surface, catalyst morphology, and thermal treatment were tested to explain the photocatalytic concentration decrease of nitrogen oxides. According to our working conditions, the conversion rates increased until an optimal value of the TiO2 weight, 35% of NO concentration and around 20% of NOx, was decomposed by the photocatalysis. The NOx removal increased proportionally with the irradiated geometric surface. The structural transformation of anatase to rutile performed by thermal treatment involved the decrease of the photocatalytic activity.  相似文献   
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