全文获取类型
收费全文 | 490篇 |
免费 | 10篇 |
国内免费 | 103篇 |
专业分类
安全科学 | 12篇 |
废物处理 | 41篇 |
环保管理 | 40篇 |
综合类 | 275篇 |
基础理论 | 51篇 |
污染及防治 | 45篇 |
评价与监测 | 139篇 |
出版年
2023年 | 14篇 |
2022年 | 6篇 |
2021年 | 9篇 |
2020年 | 17篇 |
2019年 | 6篇 |
2018年 | 13篇 |
2017年 | 9篇 |
2016年 | 17篇 |
2015年 | 27篇 |
2014年 | 22篇 |
2013年 | 32篇 |
2012年 | 24篇 |
2011年 | 28篇 |
2010年 | 24篇 |
2009年 | 23篇 |
2008年 | 12篇 |
2007年 | 31篇 |
2006年 | 33篇 |
2005年 | 26篇 |
2004年 | 18篇 |
2003年 | 30篇 |
2002年 | 24篇 |
2001年 | 28篇 |
2000年 | 19篇 |
1999年 | 14篇 |
1998年 | 19篇 |
1997年 | 14篇 |
1996年 | 26篇 |
1995年 | 10篇 |
1994年 | 10篇 |
1993年 | 7篇 |
1992年 | 8篇 |
1991年 | 2篇 |
1989年 | 1篇 |
排序方式: 共有603条查询结果,搜索用时 15 毫秒
61.
本文研究了钴(Ⅱ)催化过氧化氢氧化苯基荧光酮的褪色反应,测定了反应级数和表观活化能,建立了测定痕量地的新方法。25℃时本法检出限为29×10-13g/ml,线性范围为0.04~2ng/10ml,催化反应表观活化能为56.15KJ/mol。该方法己用于维生素B12、人发和茶叶中痕量钴的测定.结果满意,相对标准偏差为2.4~3.4%。 相似文献
62.
氨氮自动分析仪是根据纳氏试剂分光光度法的原理,通过自动进样,自动蒸馏,来实现快速准确的分析水质氨氮样品。近年来,氨氮自动分析仪广泛应用于环境监测领域,该方法能够快速、准确、方便地测定水质中的氨氮。利用标准方法纳氏试剂分光光度法进行实验室内的比对实验,通过实验分析,氨氮自动分析仪的分析曲线线性较好,相关系数达到0.9998,方法检出限、准确率和精密度能够满足当前环境监测标准的要求,实际样品测定结果理想,适合在环境监测领域推广应用。 相似文献
63.
R. Sahraei A. Farmany S. S. Mortazavi M. Roushani S. Sobhanardakani M. Ghoochian 《毒物与环境化学》2013,95(2):214-220
A method is reported for the determination of methyl violet in the range of 10–120 nmol L?1. The method is based on the catalytic effect of silver nanoparticles (AgNPs) on the oxidation reaction of methyl violet by potassium bromate in acid medium. The reaction is followed spectrophotometrically by measuring the change in absorbance () at 620 nm using a fixed time method. The reaction variables were optimized in order to achieve highest sensitivity. The 3б criterion detection limit was 5 nmol L?1, and the relative standard deviation for ten replicate determinations at a concentration of methyl violet of 15 nmol L?1 was 0.97% (n = 10). The method was successfully applied to the determination of methyl violet in river water samples. 相似文献
64.
《环境科学学报(英文版)》2023,35(7):139-151
This study investigated the enhancement effects of dissolved carbonates on the peroxymonosulfate-based advanced oxidation process with CuS as a catalyst. It was found that the added CO32− increased both the catalytic activity and the stability of the catalyst. Under optimized reaction conditions in the presence of CO32−, the degradation removal of 4-methylphenol (4-MP) within 2 min reached 100%, and this was maintained in consecutive multi-cycle experiments. The degradation rate constant of 4-MP was 2.159 min−1, being 685% greater than that in the absence of CO32− (0.315 min−1). The comparison of dominated active species and 4-MP degradation pathways in both CO32−-free and CO32−-containing systems suggested that more CO3•−/1O2 was produced in the case of CO32−deducing an electron transfer medium, which tending to react with electron-rich moieties. Meanwhile, Characterization by X-ray photoelectron spectroscopic and cyclic voltammetry measurement verified CO32− enabled the effective reduction of Cu2+ to Cu+. By investigating the degradation of 11 phenolics with different substituents, the dependence of degradation kinetic rate constant of the phenolics on their chemical structures indicated that there was a good linear relationship between the Hammett constants σp of the aromatic phenolics and the logarithm of k in the CO32−-containing system. This work provides a new strategy for efficient removal of electron-rich moieties under the driving of carbonate being widely present in actual water bodies. 相似文献
65.
The effects of employing activated Al2O3 during the catalytic pyrolysis of waste printed circuit boards (WPCBs) are investigated, focusing on the recycling of light oil. Variations in the pyrolysis process are studied through analysis of the phase distribution, water content and boiling point fractions of the resulting products. Product composition and carbon number distribution are analyzed using gas chromatography techniques. The use of activated Al2O3 increases the light oil fraction and also reduces the quantity of brominated products formed. It was determined that the best yield of light oil and most efficient debromination resulted from catalytic pyrolysis at 600 °C. Applying catalyst-to-feed ratios in the range of 1.0–1.5 also maximizes the yield of light oil. The major oil fraction resulting from catalytic pyrolysis has a boiling point range of 0–250 °C and carbon number range of C6–C9, showing for use as a potential fuel after suitable treatment such as hydrogenation. At a higher catalyst-to-feed ratio of 2.0, activated Al2O3 generates a high proportion of light oil fractions containing a significant quantity of chemicals such as phenol (52.67% at 600 °C), although an overall lower yield of oil is obtained. The oil produced in this manner may also be used as a raw material feedstock for the production of various other useful chemicals. 相似文献
66.
Cu–Mn, Cu–Mn–Ce, and Cu–Ce mixed-oxide catalysts were prepared by a citric acid sol–gel method and then characterized by XRD, BET, H2-TPR and XPS analyses. Their catalytic properties were investigated in the toluene combustion reaction. Results showed that the Cu–Mn–Ce ternary mixed-oxide catalyst with 1:2:4 mole ratios had the highest catalytic activity, and 99% toluene conversion was achieved at temperatures below 220°C. In the Cu–Mn–Ce catalyst, a portion of Cu and Mn species entered into the CeO2 fluorite lattice, which led to the formation of a ceria-based solid solution. Excess Cu and Mn oxides existed on the surface of the ceria-based solid solution. The coexistence of Cu–Mn mixed oxides and the ceria-based solid solution resulted in a better synergetic interaction than the Cu–Mn and Cu–Ce catalysts, which promoted catalyst reducibility, increased oxygen mobility, and enhanced the formation of abundant active oxygen species. 相似文献
67.
催化动力学光度法测定痕量铈 总被引:6,自引:0,他引:6
根据前量铈在稀硫酸介质中对重铬酸根氧化EDTA而褪色的反应有催化作用,建立了测定痕量铈的新动力学光度法,测定范围为0 ̄2.4×10^-2μg/mL,检限限为5.2×10^-10g/mL,用于测定人发中的痕量铈,结果满意。 相似文献
68.
稀土金属具有一些特殊的性能,这使得其对碳质材料还原NO的反应可能表现出特殊的催化效果,而此方面的研究没有报道.为了研究稀土金属对活性炭还原NO反应的催化效果,采用浸渍法制备了负载氧化镧的活性炭颗粒(La/C),并在无氧的固定床反应器中进行了程序升温反应和等温反应,考察了气体流量、NO的入口浓度、反应温度和氧化镧负载量对反应活性的影响,同时对反应机理和动力学进行了初步探讨.研究结果表明负载氧化镧的活性炭还原NO的反应是一级反应.由于炭表面3%(质量分数)的氧化镧的存在,C-NO反应的起始反应温度从500 ℃降低到300 ℃,反应活性大大提高,反应活化能从88.95 kJ/mol降低到51.05 kJ/mol.氧化镧的负载量对反应活性有重要影响,但负载量的大量增加对反应活性的提高效果甚微,最佳负载量为1.5%.La/C体系在反应中较稳定,而反应温度的升高对其稳定性不利. 相似文献
69.
环境样品中痕量锰的催化动力学测定法 总被引:2,自引:0,他引:2
对环境样品中痕量锰的催化动力学测定方法进行简要评述,引述文献16篇。 相似文献
70.