全文获取类型
收费全文 | 764篇 |
免费 | 105篇 |
国内免费 | 522篇 |
专业分类
安全科学 | 148篇 |
废物处理 | 61篇 |
环保管理 | 56篇 |
综合类 | 724篇 |
基础理论 | 128篇 |
污染及防治 | 243篇 |
评价与监测 | 20篇 |
社会与环境 | 4篇 |
灾害及防治 | 7篇 |
出版年
2024年 | 3篇 |
2023年 | 21篇 |
2022年 | 29篇 |
2021年 | 49篇 |
2020年 | 37篇 |
2019年 | 39篇 |
2018年 | 37篇 |
2017年 | 37篇 |
2016年 | 64篇 |
2015年 | 74篇 |
2014年 | 62篇 |
2013年 | 66篇 |
2012年 | 81篇 |
2011年 | 77篇 |
2010年 | 54篇 |
2009年 | 64篇 |
2008年 | 44篇 |
2007年 | 88篇 |
2006年 | 72篇 |
2005年 | 43篇 |
2004年 | 38篇 |
2003年 | 49篇 |
2002年 | 28篇 |
2001年 | 30篇 |
2000年 | 25篇 |
1999年 | 38篇 |
1998年 | 31篇 |
1997年 | 23篇 |
1996年 | 13篇 |
1995年 | 15篇 |
1994年 | 15篇 |
1993年 | 18篇 |
1992年 | 7篇 |
1991年 | 6篇 |
1990年 | 3篇 |
1989年 | 5篇 |
1988年 | 2篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1978年 | 1篇 |
1977年 | 1篇 |
排序方式: 共有1391条查询结果,搜索用时 171 毫秒
81.
Bappaditya Kanrar Anjan Bhattacharyya 《Journal of environmental science and health. Part. B》2013,48(8):788-797
The photolysis of a rice herbicide Bispyribac sodium (Sodium 2, 6-bis [(4, 6-dimethoxypyrimidin-2-yl) oxy] benzoate) has been studied in different aqueous medium (distilled water, pond water and Irrigation water) under the influence of UV (λ max ≥ 250 nm) and sunlight in presence or absence of sensitizers (TiO2 and KNO3). The study was conducted under laboratory simulated condition which made it possible to evaluate the contribution of different factors viz. source of irradiation, solvent and sensitizers towards the photolysis of bispyribac sodium. The photodegradation proceeds via first order reaction Kinetics in all the cases. Five photo metabolites (M1-M5) were isolated in pure form by column chromatographic method from the irradiation system under UV influenced and TiO2 as sensitizer. From the different spectral data (IR, NMR, UV-VIS, Mass) the structure of these five metabolites were assigned as M1 (Phenol), M2 [2, 6-Dihydroxy benzoic acid], M3 [2, 6-bis [(4, 6 dimethoxypyrimidin-2yl) oxy] benzoic acid], M4 [2-(3-Hydroxy-phenoxy)-pyrimidine-4, 6-diol] and M5 as [2,4-Dihydroxy-3, 5-dimethoxy-6-(4-methoxy pyrimidine-2-yloxy)-benzoic acid]. Moreover, another six photometabolites (M6-M11) were identified from the different irradiation system on the basis of Micromass analysis. On the basis of MS/MS data analysis, the structure of these six photometabolites were assigned as M6 [2-(4, 6-Dimethoxy-pyrimidin-2-yloxy)-6-hydroxy-benzoic acid], M7 [2-Hydroxy-6-(4-hydroxy-6-methoxy-pyrimidin-2-yloxy)-benzoic acid], M8 [4, 6-Dimethoxy-pyrimidin-2-ol], M9 [6-Methoxy-pyrimidine-2, 4-diol], M10 [2-Hydroxy-6-(pyrimidin-2-yloxy)-benzoic acid] and M11 [2, 4, 6-Trimethoxy-pyrimidine]. The plausible Photodegradation pathways of bispyribac sodium in the present investigation were portrayed which proceeds via hydrolysis, hydrolytic cleavage, O-dealkylation, decarboxylation, dehydroxylation, O-alkylation and hydroxylation. 相似文献
82.
以地水中的氯代烃污染物三氯乙烯(TCE)为目标污染物,以过硫酸钾溶液为氧化剂,探讨了不同条件下过硫酸钾对TCE的去除效果。实验结果表明,在40℃,过硫酸钾初始浓度为2.43 g/L条件下,反应2 h后,TCE的去除率就可达到96.8%;过硫酸钾对TCE的去除符合一级反应动力学方程,速率常数(K)为1.3364 h-1,半衰期(t1/2)为0.51 h;过硫酸钾对TCE的去除速率在pH为中性附近时最大,其后无论pH升高或降低去除速率均减小;受温度和pH影响较明显,并且反应温度越高,受pH的影响越明显;随离子强度的增加而减小;反应活化能为119.6 kJ/mol;过硫酸钾溶于水生成过硫酸根离子(S2O28-),S2O28-会进一步生成硫酸根自由基(SO4-.),在碱性条件下,SO4-.与OH-反应会进一步生成羟基自由基(.OH)。过硫酸钾对于TCE的去除主要源自SO4-.和.OH的强氧化性。 相似文献
83.
84.
This study investigated environmental distributions and production mechanisms of chlorinated polycyclic aromatic hydrocarbons (Cl-PAHs) in the sediments from some tidal flats located in Asia. Cl-PAHs were found in sediments taken from Arao tidal flat, Kikuchigawa River and Shirakawa River. The range of ∑Cl-PAHs was from 25.5 to 483 pg g−1 for Kikuchigawa River and Arao tidal flat, respectively.Concentrations of PAHs and Cl-PAHs showed no significant correlations (r = 0.134). This result suggests that the origins of these compounds differ. In the identified Cl-PAH isomers, the most abundant Cl-PAH isomer was 9,10-dichloroanthracene (9,10-di-Cl-ANT) in the three sites. In general, concentrations of Cl-ANTs in the coastal environment are about 3-5 orders of magnitude lower than those of anthracene (ANT). However, concentration ratios between Cl-ANTs and ANT (Cl-ANTs/ANT) in the sediments ranged from 4.1% to 24.6%. This result indicated that Cl-PAHs were not generated under industrial processes but the high concentration ratios have resulted from the contribution of photochemical production of Cl-ANTs in the sediments because ANT is known to have high photochemical reactivity.For examining this phenomenon, ANT adsorbed onto glass beads was irradiated with UV under the mimicked field conditions of tidal flats. As a result, it was noticed that, while chlorinated derivatives were negligible in a light-controlled group, production of 2-Cl-ANT, 9-Cl-ANT and 9,10-diCl-ANT on the irradiated surface were found in this study. These results suggest that photochemical reaction of PAHs can be a potential source of the occurrence of Cl-PAHs in the coastal environment. 相似文献
85.
Moe MK Huber S Svenson J Hagenaars A Pabon M Trümper M Berger U Knapen D Herzke D 《Chemosphere》2012,89(7):869-875
For several decades, perfluorooctane sulfonate (PFOS) has widely been used as a fluorinated surfactant in aqueous film forming foams used as hydrocarbon fuel fire extinguishers. Due to concerns regarding its environmental persistence and toxicological effects, PFOS has recently been replaced by novel fluorinated surfactants such as Forafac®1157, developed by the DuPont company. The major component of Forafac®1157 is a 6:2 fluorotelomer sulfonamide alkylbetaine (6:2 FTAB), and a link between the trade name and the exact chemical structure is presented here to the scientific community for the first time. In the present work, the structure of the 6:2 FTAB was elucidated by 1H, 13C and 19F nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry. Moreover, its major metabolites from blue mussel (Mytilus edulis) and turbot (Scophthalmus maximus) and its photolytic transformation products were identified. Contrary to what has earlier been observed for PFOS, the 6:2 FTAB was extensively metabolized by blue mussel and turbot exposed to Forafac®1157. The major metabolite was a deacetylated betaine species, from which mono- and di-demethylated metabolites also were formed. Another abundant metabolite was the 6:2 fluorotelomer sulfonamide. In another experiment, Forafac®1157 was subjected to UV-light induced photolysis. The experimental conditions aimed to simulate Arctic conditions and the deacetylated species was again the primary transformation product of 6:2 FTAB. A 6:2 fluorotelomer sulfonamide was also formed along with a non-identified transformation product. The environmental presence of most of the metabolites and transformation products was qualitatively demonstrated by analysis of soil samples taken in close proximity to an airport fire training facility. 相似文献
86.
Fe2O3-Cr2O3/TiO2系列催化剂的结构和脱硝性能 总被引:1,自引:0,他引:1
研究以纳米TiO2为载体,浸渍负载过渡金属氧化物,以CO为还原剂的脱硝催化剂的脱硝性能。实验中以计算量的Ni(NO3)2和Fe(NO3)3混合溶液浸渍纳米TiO2粉末,室温下搅拌30 min至混合均匀,放入旋转蒸发器中,70℃下至水分蒸干为止;所得粉末在550℃下、空气气氛中焙烧4 h即得所需催化剂。用以上方法分别制备2%Fe2O3-10%Cr2O3/TiO2、4%Fe2O3-8%Cr2O3/TiO2、6%Fe2O3-6%Cr2O3/TiO2、8%Fe2O3-4%Cr2O3/TiO2与10%Fe2O3-2%Cr2O3/TiO2等5种催化剂样品。实验结果表明,制备的催化剂具有较好的结构,分散较为均匀。对于CO+NO反应,Fe2O3-Cr2O3/TiO2系列催化剂具有较好的催化活性,NO的转化率都达到了100%。其中,10%Fe2O3-2%Cr2O3/TiO2样品具有最好的低温活性,H2-TPR结果表明,这是由于10%Fe2O3-2%Cr2O3/TiO2催化剂更易于被CO预还原。 相似文献
87.
微波诱导AC/Cu、AC/Fe催化非均相Fenton 反应催化降解垃圾渗滤液 总被引:1,自引:0,他引:1
采用活性炭载体负载Cu、Fe为催化剂,在微波诱导作用下,对垃圾渗滤液污染物进行降解。实验结果表明,活性炭负载金属前经适当浓度硝酸浸泡处理后,催化剂对COD去除率提高可超过15%,过高硝酸盐浓度对COD去除有不利影响;催化剂对COD去除率随Cu、Fe金属负载量增加呈先增加后降低的趋势,催化剂对Cu、Fe的最佳负载量分别为质量百分比2.11%和1.12%。对于AC-Cu体系,在初始pH=3,H2O2投加量为4.98×103mg/L,催化剂用量为5.0×103mg/L,420 W功率下微波辐射10 min时,垃圾渗滤液COD去除率可达到84.13%;对于AC-Fe体系,当H2O2投加量为0.33×103mg/L,催化剂AC-Fe用量为2.0×104mg/L,420 W功率下微波作用10 min时,垃圾渗滤液COD去除率为60.16%。分析2种催化剂对COD去除差异的原因,可能是催化剂AC-Cu表面单分子分布的阈值比AC-Fe高。降解液的pH值对AC-Cu体系、AC-Fe体系COD去除影响存在拐点,最高COD去除率点对应的降解液pH值为3。微波辐射功率较低时,体系COD去除率随辐射功率增加而增加;辐射功率较高时,高温下垃圾渗滤液中有机硫化物分解成小分子硫化物,对催化剂活性存在一定抑制作用。 相似文献
88.
89.
TAIC(三烯丙基异氰脲酸酯)作为过氧化物交联或自由基反应交联的助交联剂被广泛应用。由于TAIC性质稳定难于生物降解,采用铁炭微电解法处理TAIC生产废水,并考察了铁炭比、进水pH值、反应时间对处理效果的影响,以及TAIC降解机理和反应动力学过程。结果表明,影响微电解工艺的因素主次关系为:pH>Fe/C质量比>反应时间;在最佳条件进水pH值为5,铁炭质量比为2:1,反应时间为135 min时,COD的去除率达到46%以上,TAIC的去除率达到48%以上。TAIC去除机理研究表明,微电解对TAIC废水的作用主要通过·H的还原和铁离子的絮凝作用,其中·H的还原作用是TAIC降解的主要原因。反应动力学分析表明,铁炭微电解法处理TAIC的降解过程基本符合二级反应动力学规律,通过建立模型并拟合出了TAIC降解的二级反应动力学方程。 相似文献
90.
The influence of intact (FLT) and photomodified (phFLT) fluoranthene (0.05, 0.5 and 5 μmol l−1) and herbicide Basagran (5, 20, 35 and 50 nmol l−1) on the germination, growth of seedlings and photosynthetic processes in pea plants (Pisum sativum L., cv. Garde) was investigated. The germination was significantly inhibited already by the lowest concentration (0.05 μmol l−1) of FLT and phFLT, while Basagran caused inhibition only in higher concentrations (35 and 50 nmol l−1). The growth of roots was significantly inhibited by higher concentration 5 μmol l−1 of both FLT and phFLT and the shoot of seedlings was significantly influenced only by photomodified form. The length of root and shoot was inhibited already by concentration 5 nmol l−1 of Basagran. Organic compounds applied on chloroplasts suspension influenced primary photochemical processes of photosynthesis. In chlorophyll fluorescence parameters, the significant increase of F0 values and the decrease of FV/FM and ΦII values by application of FLT (0.5 and 5 μmol l−1) and phFLT (0.05, 0.5 and 5 μmol l−1) was recorded. The maximum capacity of PSII (FV/FM) was influenced by the highest (50 nmol l−1) and the effective quantum yield of PSII (ΦII) already by the lowest (5 nmol l−1) concentration of Basagran. Hill reaction activity decreased and was significantly inhibited by higher concentration (0.5 and 5 μmol l−1) of FLT and phFLT and already by the lowest concentration (5 nmol l−1) of Basagran. 相似文献