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161.
162.
构建具有不同蚯蚓和植物配置的4个单级蚯蚓生态滤池,依次编号为A(无蚯蚓无植物)、B(有蚯蚓无植物)、C(有蚯蚓栽种芦苇)和D(有蚯蚓栽种水生鸢尾)。通过比较4个滤池在6个月实验期间对化学需氧量(COD)和总氮(TN)的去除效率,系统分析蚯蚓和植物对滤池去除污染物的影响。实验分2个阶段进行:5月上旬至9月上旬,滤池进水碳氮比恒定为6;9月中旬至11月中旬,滤池每周进水碳氮比交替为3、6、9。研究结果表明,蚯蚓对滤池去除COD有一定的促进作用,且作用强度显著受到进水碳氮比的影响。植物的存在与种类对滤池去除COD效率没有显著影响。蚯蚓和植物对滤池的TN去除效率都没有显著影响。滤池进水的碳氮比是显著影响滤池去除TN效率的主要因素。 相似文献
163.
玉米秸秆活性炭的制备及其吸附动力学研究 总被引:2,自引:0,他引:2
以玉米秸秆为原材料,采用ZnCl2活化法制备玉米秸秆活性炭,吸附次甲基蓝染料废水,进行动力学分析。本实验用Langmuir和Freundlich模型对吸附等温线进行拟合,结果表明,玉米秸秆活性炭对次甲基蓝的吸附与Langmuir方程拟合良好,R2=0.9857。采用Lagergren准一级速率模型、Lagergren准二级速率模型、Bangham动力学方程和Elovich动力学方程分别对秸秆活性炭吸附次甲基蓝溶液进行吸附动力学拟合,通过分析得出吸附过程与Lagergren准二级速率模型拟合最好,R2=0.9979。秸秆活性炭对次甲基蓝的最大吸附量达到909.09 mg/g,具有很高的吸附能力。 相似文献
164.
镍渣的重金属浸出特性 总被引:3,自引:0,他引:3
在分析镍渣的矿物相组成和重金属元素含量的基础上,鉴定了镍渣样品的浸出毒性,并考察了pH、液固比和浸出时间等条件对镍渣样中铬、铅、铜和锌等重金属浸出特性的影响。结果表明,镍渣中的重金属总量约为渣样的0.9%,且铬、铜和锌的含量较高,需进行安全管理。实验所用镍渣样品为第Ⅰ类一般工业固体废物。在强酸条件下镍渣中重金属浸出浓度较大,pH3后浸出浓度显著降低;液固比40 L/kg时,镍渣中重金属不断溶出,液固比40 L/kg后,浸出达到饱和,浸出浓度趋于平衡;随着浸出时间的增加,重金属离子的浸出浓度先增加后减少,但由于各重金属性质不同,各重金属达到最大浸出浓度的时间不同。 相似文献
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Bin Xu Tingyao Gao Chenyan Hu Jiekuan Shi 《Journal of the Air & Waste Management Association (1995)》2013,63(6):714-718
Abstract This paper introduces a new allocation method on discharge loading of each function zone in a total emission control region. The wind frequency, the position of each district, and the pollutant’s influence area were taken into account in this new method. The concept of “average downwind distance” was brought forward in this paper. The method here is more reasonable than the original method of area distribution, which was proposed by the “A-value” method in regulation of total emissions in China, by means of the simulation of annual average concentration in the total emission control region. 相似文献
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Increasing antibacterial resistance and pathogenicity in the environment is of growing concern due to its potential human risk. In the present study, 236 Escherichia coli isolates were collected from Wenyu River in China on drugless (48 isolates) and quinolone-containing plates (189 isolates). Their minimum inhibitory concentrations (MICs) were determined ranging from 0.125 μg mL−1 to 128 μg mL−1. Mutation points related to fluoroquinolone resistance were observed at S83 to L and D87 to N or Y in the GyrA subunit and S80 to R or I and E84 to G in the ParC subunit. Generally, MICs of LEV and GAT are dependent on the patterns of these mutation points. The profile with three mutation points was related to LEV-resistant E. coli isolates, and the (S83L, D87N + S80I) mutation profile was most prevalent (65.7%) in LEV-resistant isolates, while a large proportion of isolates, even those with three mutation points, were susceptive to GAT. The incidence of virulence factors in LEV-resistant isolates (44.7%, 59/132) was much higher than in nonresistant isolates (23.1%, 24/104) (χ2 = 11.925, 1° of freedom, p < 0.001) indicating that fluoroquinolone-resistant E. coli would pose a potential risk. A similar distribution was also found in isolates resistant to GAT (χ2 = 7.843, 1° of freedom, p = 0.0079). 相似文献
170.
Tao Tang Kun QianTianyu Shi Fang WangPingliang Li Jianqiang LiYongsong Cao 《Chemosphere》2012,89(11):1419-1425
Quinestrol is synthetic estrogen used in contraceptive and hormone replacement therapy and occasionally for treating breast cancer and prostate cancer. It can make its way into the environment through sewage discharge and waste disposal produced by human excretions. In this study, the photodegradation kinetics of quinestrol in various conditions was investigated by UV and solar irradiation. The affecting factors were studied including concentration of hydrogen peroxide, different water types, and the initial concentrations of quinestrol. Concurrently, the transformation products and presumed pathways of quinestrol in distilled water by UV irradiation were identified and proposed. The results showed that the degradation of quinestrol in both irradiation conditions followed the pseudo-first-order kinetics. More rapid degradation was observed by UV irradiation (k = 0.018 min−1) than solar irradiation (k = 0.004 h−1), and the photodegradation rate of quinestrol depended on the concentration of hydrogen peroxide, the initial concentration of quinestrol and water types. The transformation products of quinestrol in distilled water were identified by gas chromatography/mass spectrometry. When exposed to UV irradiation, quinestrol in aqueous solution was rapidly degraded, giving at least ten photodegradation products. The chemical structures of ten degradation products were identified on the basis of mass spectrum interpretation and literature data. 相似文献