全文获取类型
收费全文 | 250篇 |
免费 | 43篇 |
国内免费 | 140篇 |
专业分类
安全科学 | 16篇 |
废物处理 | 71篇 |
环保管理 | 15篇 |
综合类 | 212篇 |
基础理论 | 38篇 |
污染及防治 | 76篇 |
评价与监测 | 5篇 |
出版年
2024年 | 1篇 |
2023年 | 6篇 |
2022年 | 2篇 |
2021年 | 3篇 |
2020年 | 4篇 |
2019年 | 9篇 |
2018年 | 16篇 |
2017年 | 5篇 |
2016年 | 12篇 |
2015年 | 32篇 |
2014年 | 25篇 |
2013年 | 23篇 |
2012年 | 34篇 |
2011年 | 29篇 |
2010年 | 17篇 |
2009年 | 24篇 |
2008年 | 11篇 |
2007年 | 24篇 |
2006年 | 40篇 |
2005年 | 31篇 |
2004年 | 19篇 |
2003年 | 20篇 |
2002年 | 14篇 |
2001年 | 7篇 |
2000年 | 8篇 |
1999年 | 3篇 |
1998年 | 5篇 |
1997年 | 3篇 |
1996年 | 5篇 |
1995年 | 1篇 |
排序方式: 共有433条查询结果,搜索用时 31 毫秒
21.
22.
23.
土壤颗粒对纳米TiO_2悬浮稳定性作用机制的实验研究 总被引:1,自引:1,他引:0
在不含表面活性剂和含有表面活性剂两种条件下,研究了土壤颗粒对纳米TiO2(nTiO2)悬浮稳定性的影响.结果表明,土壤颗粒降低了nTiO2在水相中的悬浮稳定性.当体系中不含表面活性剂时,nTiO2在土壤大颗粒上的沉积是导致nTiO2脱稳沉淀的主要原因.在含有表面活性剂的溶液中,土壤颗粒降低nTiO2悬浮稳定性的作用变得更加明显了.一方面,表面活性剂加速了土壤颗粒本身的沉降从而增强了nTiO2在其中的沉降,另一方面,表面活性剂在土壤上的强烈吸附促进了表面活性剂-nTiO2在土壤上的沉积.扫描电镜显示,nTiO2不仅吸附在土壤大颗粒上,还会吸附在土壤小颗粒表面.3种表面活性剂中,十六烷基三甲基溴化铵(CTAB)悬浮的nTiO2与土壤颗粒共沉淀现象最明显.除了土壤对CTAB的吸附作用之外,XDLVO/DLVO能量计算显示CTAB体系中土壤颗粒与nTiO2之间存在显著第二极小值,表明nTiO2能够在第二极小值位置与土壤颗粒结合,从而与土壤颗粒一起快速沉淀. 相似文献
24.
Carbon tetrachloride (CCl4) is a toxic chemical that was once used in degreasers and detergents, and some remnants of the chemical may be present in the water supply. Physiologically-based pharmacokinetic (PBPK) modeling can assist in understanding resulting internal doses of CCl4 after exposure, but the pharmacokinetic parameters describing the metabolism of CCl4 are not well characterized. The goal of this study was to provide insights into how to more accurately estimate these values in rats using PBPK modeling and data from previous studies. Three different PBPK models were constructed to describe CCl4 exposure in rats via inhalation, oral ingestion, and venous injection. Each of these models was compared to data, and sensitivity analysis was performed for each model to determine whether the available data could be used to accurately determine the metabolic parameters of interest. These parameter sensitivities were so low that optimization to the available data yielded physiologically unrealistic results. Model sensitivities were analyzed for different doses and routes of exposure in order to find experimental conditions that would allow for greater identifiability of the metabolic parameters. Data were simulated from these models at optimal conditions with varying levels of noise from a normal distribution. Optimizations were then performed to confirm that the original values could be obtained. The experiments developed are left as suggestions for investigators who wish to further pursue estimating these metabolic parameters. 相似文献
25.
Preparation and performance of photocatalytic regenerationable activated carbon prepared via sol-gel TiO2 总被引:1,自引:0,他引:1
Preparation of photocatalytic regenerationable activated carbon (AC) is the key step for the practical application of in situ regeneration of exhausted AC. A novel photocatalytic regenerationable AC was prepared by sol-gel TiO2 in this work. The adsorption and regeneration performance of TiO2/AC were evaluated using phenol as model compound. Scanning electron microscope (SEM) and nitrogen (77 K) adsorption isotherm were used to determine the surface area, pore structure and the distribution of TiO2. The results showed that with the increase of TiO2 loading, adsorption capacity of TiO2/AC decreased and the regeneration efficiency increased. The photocatalytic regenerationable AC with suitable TiO2 loading (2 wt%) exhibited suitable adsorption capacity and regeneration efficiency. TiO2 located mainly in the entrance of macro-pore of carbon. The prepared TiO2/AC exhibited similar surface structure and pore structure with material carbon. 相似文献
26.
近二十年来发展起来的光催化技术可利用太阳光能对水体中的多种有机污染物进行降解.这符合可持续发展的长远需要,具有诱人的发展前景。光催化技术利用可再生的清洁资源,氧化能力强.适用于广谱有机物,能使难被一般氧化剂氧化、又难生物降解的污染物降解.是当前太阳能利用及水污染控制方面开辟的前沿领域.在治理环境污染方面具有明显的发展优势。本文以溶胶-凝胶法、金属有机化学气相淀积、煅烧沉淀法等多种方法制备光活性二氧化钛膜。 相似文献
27.
28.
29.
30.
Model reactor for photocatalytic degradation of persistent chemicals in ponds and waste water 总被引:10,自引:0,他引:10
A laboratory scale flow-through model reactor for the degradation of persistent chemicals using titanium dioxide (TiO2) as photocatalyst immobilized on glass beads is presented. In the test system with a volume of 18 L contaminated water is pumped to the upper part of the floating reactor and flows over the coated beads which are exposed to UV-radiation. The degradation of two dyes of different persistance was investigated. Primary degradation of methylene blue did not fit a first order kinetic due to coincident adsorption onto the photocatalyst and direct photolysis, resulting in a half-life of 6 h. A filtrate of a green algae suspension accelerated the colour removal. In contrast, reactive red 2 was degraded only by photocatalysis; neither adsorption nor direct photolysis led to a colour removal. The course of primary degradation followed a first order kinetic with a half-life of 18 h and a rate constant of 0.04 h−1. Analysis of the degradation products indicated mineralization by detection of NO2− and NO3−, accompanied by a decrease of pH and an increase of conductivity. A successful adaptation of the model reactor (scale 1:10) to dimensions required for surface waters and waste water treatment plants would be a costefficient and environmentally sustainable application of photocatalysis for the treatment of industrially polluted water and could be of relevance for third world contries, particularly those favoured by high solar radiation. 相似文献