全文获取类型
收费全文 | 43篇 |
免费 | 9篇 |
国内免费 | 21篇 |
专业分类
安全科学 | 5篇 |
废物处理 | 1篇 |
环保管理 | 1篇 |
综合类 | 44篇 |
基础理论 | 7篇 |
污染及防治 | 6篇 |
评价与监测 | 5篇 |
社会与环境 | 4篇 |
出版年
2023年 | 1篇 |
2022年 | 2篇 |
2021年 | 3篇 |
2020年 | 3篇 |
2018年 | 2篇 |
2017年 | 2篇 |
2016年 | 1篇 |
2015年 | 6篇 |
2014年 | 4篇 |
2013年 | 4篇 |
2012年 | 8篇 |
2011年 | 1篇 |
2010年 | 4篇 |
2009年 | 3篇 |
2008年 | 2篇 |
2006年 | 1篇 |
2005年 | 5篇 |
2004年 | 3篇 |
2002年 | 4篇 |
2001年 | 3篇 |
2000年 | 2篇 |
1999年 | 1篇 |
1998年 | 1篇 |
1997年 | 3篇 |
1994年 | 2篇 |
1989年 | 1篇 |
1988年 | 1篇 |
排序方式: 共有73条查询结果,搜索用时 31 毫秒
51.
52.
青藏高原纳木错流域河水主要离子化学特征及来源 总被引:19,自引:12,他引:7
2006年6~10月对青藏高原纳木错流域你亚曲、曲嘎切、昂曲3条河流进行了连续采样,同时在2005年9月和2006年9月2次环纳木错考察中采集了其他河水的样品.河水中主要阴离子(Ca2+、 Mg2+、 Na+、 K+)和阳离子(Cl-、 NO-3、 HCO-3、 SO2-4)的分析结果表明,你亚曲、曲嘎切和昂曲的离子总量(TDS)分别为79.48、 23.44和111 mg/L.离子总量明显低于青藏高原及我国其他河流,且相互之间存在较为明显的差距. 3条河流中,曲嘎切为重碳酸盐钙型水,昂曲介于重碳酸盐钠型和重碳酸盐钙型之间,你亚曲的化学类型介于两者之间.河流水化学的时间变化显著,而且与流量成一定的反相关关系.利用主成分分析和相关分析得出:你亚曲河水主要化学成分来源于碳酸盐中的Ca2+和HCO-3;曲嘎切来源于冰川融水以及碳酸盐中的Ca2+、HCO-3和Na+;昂曲则来源于蒸发岩中的Na+、Mg2+和Cl-. 相似文献
53.
西藏中部巴木错湖泊面积变化及其原因分析 总被引:1,自引:0,他引:1
受气候变化影响,西藏中部内陆湖泊在最近10 a来出现了水位上涨、湖面扩大等情况。采用遥感技术及统计学方法分析了西藏中部巴木错湖泊面积年内、年际变化及其原因。结果表明:①湖泊周边班戈站的年降水量、年平均气温、年平均地温以及年平均相对湿度等呈现增加趋势,年平均风速显现下降趋势;②2009年的面积在2月、5月和8月出现了三个"峰值",主要与湖面封冻、气温升高及降水增加等有关,年际变化呈逐步增加趋势;③经线性相关、多元回归等分析发现,年内变化受各月面降水量AP、蒸发量E和气温T的影响,合计贡献率为90.0%,排序为AP>E>T;年际变化受年平均风速SWS、7月降水量P7、平均地温ST和气温T的影响,合计贡献率为65.2%,排序为SWS>P7>ST>T。 相似文献
54.
Takashi Itakura David W. Airey Chin Jian Leo Gordon D. McOrist 《Journal of environmental radioactivity》2010,101(9):723-1087
Tests using reconstituted samples have been performed to assess the diffusive transport of 137Cs and 60Co through natural regolith materials from a region in South Australia being considered for a radioactive waste repository. A double diffusion cell apparatus made of polycarbonate resin was developed to estimate the effective diffusion (De) and sorption coefficients (Kd) that allowed large withdrawals from the source and collector cells and has enabled tests with low concentrations of radioactivity. An alternative to porous stainless steel filter plates has also been used to reduce uncertainty in test interpretation. Analysis of the transient data used a staged method of the Laplace transform to take into consideration the volume of the samples withdrawn from the apparatus during testing. At test completion samples were cut into slices and analysed for radionuclide concentration. Data obtained from the sliced samples confirmed that both numerical and experimental data produced acceptable mass balance. The De values obtained in this study were of the order of 10−6 cm2 s−1 for both species, higher than previously published data. The Kd values from the diffusion and batch sorption tests were in reasonable agreement for 137Cs, but an order of magnitude different for 60Co. The sorption of the latter radionuclide was strongly pH dependent, and this dependency during diffusion tests would benefit from further investigation. 相似文献
55.
新疆某地土壤中有效态钴提取法研究 总被引:1,自引:0,他引:1
采用火焰原子吸收光谱法测定比较了EDTA、柠檬酸、DTPA-TEA、Ca(NO3)2和NH4OAc 5种浸提剂对新疆某石化企业污水库周边农田土壤中有效态钴的浸提效果,并将超声浸提法引入常规振荡提取中.采用Tessier连续提取法对试验土壤进行形态分析,并分析了各形态钴与单一浸提剂提取钻量的相关性.结果表明,不同浸提剂对土壤有效态钴的提取率明显不同,提取率均随土壤钴含量升高而升高.浸提剂对有效钴的提取率从大到小依次为柠檬酸、EDTA、DTPA-TEA、NH4OAc、Ca(NO3)2;5种浸提剂的超声法提取钴量均高于常规振荡法,且EDTA提高程度最大.通过紫花苜蓿盆栽试验可知,柠檬酸、EDTA和DTPA-TEA提取有效态钴量与紫花苜蓿根、茎、叶中钴质量比存在较好相关性,且它们的提取率较高,可作为土壤中有效钴的浸提剂.Tessier连续法提取的各形态钴中,5种浸提剂提取钴量与除残渣态外其余4种形态钴及紫花苜蓿根、茎、叶中富集钴量之间均有较好的相关性. 相似文献
56.
利用水热浸渍法制备了生物炭基-Co3O4复合材料(Co-OB),采用扫描电子显微镜(SEM)、X射线衍射仪(XRD)、傅里叶变换衰减全反射红外光谱仪(ATR-IR)等手段对Co-OB进行表征,并研究了其活化过一硫酸盐(PMS)降解阿特拉津(ATZ)的性能,探究了PMS投加量、腐殖酸(HA)和Cl-对ATZ降解的影响.结果表明,在Co-OB活化投加量0.025g/L,PMS浓度200μmol/L,ATZ浓度20μmol/L,室温条件下10min内ATZ的去除率为86.3%,与生物炭(OB)和Co3O4相比,其去除率为后两者之和的2.2倍.随着PMS浓度增加,ATZ去除率显著提高.Cl-、HA的存在抑制了ATZ的降解,且随Cl-、HA浓度增加,抑制程度增大.自由基猝灭实验表明·OH和SO4·-是ATZ降解的主要活性物种.通过液相色谱-质谱联用仪(LC-MS)分析出6种中间产物,并推测出ATZ的降解途径.稳定性实验表明Co-OB具有重复使用性及低Co2+溶出. 相似文献
57.
58.
A simple, sensitive column solid-phase extraction procedure for separation and preconcentration of Cu(II), Ni(II), Co(II), and Cd(II) in spiked and natural water samples using 2,3-dihydroxynaphthalene-functionalized Amberlite XAD-4 (XAD-4-DHN) chelating resin prior to their determination by inductively coupled plasma atomic emission spectrometry was discussed. The optimum experimental parameters such as pH, volume of sample and eluent, flow-rates of uptake and stripping, and sorption capacity of the chelating resin, were evaluated. The effect of the electrolytes and the cations on the preconcentration of metal ions was also investigated. The chelating resin could be reused for more than 20 cycles of sorption–desorption without any significant change (<1.0%). Recoveries obtained from this method range from 96 to 102% with R.S.D of 2.50 (n = 4). The detection limits for Cu(II), Ni(II), Co(II), and Cd(II) were found to be 1.9, 0.9, 1.2 µg, and 1.4 µg L?1, respectively. The proposed method was applied for the determination of Cu(II), Ni(II), Co(II), and Cd(II) in spiked, tap water, and river water samples. 相似文献
59.
Enhui Wu Daifeng Lin Yinye Chen Xiaoshan Feng Kui Niu Yongjin Luo Baoquan Huang Jianbin Qiu Qingrong Qian Qinghua Chen 《环境科学学报(英文版)》2022,34(6):79-89
A series of nitrogen-doped CoAlO (N-CoAlO) were constructed by a hydrothermal route combined with a controllable NH3 treatment strategy. The effects of NH3 treatment on the physico-chemical properties and oxidation activities of N-CoAlO catalysts were investigated. In comparison to CoAlO, a smallest content decrease in surface Co3+ (serving as active sites) while a largest increased amount of surface Co2+ (contributing to oxygen species) are obtained over N-CoAlO/4h among the N-CoAlO catalysts. Meanwhile, a maximum N doping is found over N-CoAlO/4h. As a result, N-CoAlO/4h (under NH3 treatment at 400°C for 4 hr) with rich oxygen vacancies shows optimal catalytic activity, with a T90 (the temperature required to reach a 90% conversion of propane) at 266°C. The more oxygen vacancies are caused by the co-operative effects of N doping and suitable reduction of Co3+ for N-CoAlO/4h, leading to an enhanced oxygen mobility, which in turn promotes C3H8 total oxidation activity dominated by Langmuir-Hinshelwood mechanism. Moreover, in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTs) analysis shows that N doping facilities the decomposition of intermediate species (propylene and formate) into CO2 over the catalyst surface of N-CoAlO/4h more easily. Our reported design in this work will provide a promising way to develop abundant oxygen vacancies of Co-based catalysts derived from hydrotalcites by a simple NH3 treatment. 相似文献
60.
为探究液相还原法制备的纳米Fe/Co催化剂的类芬顿催化效果,以单因素分析法研究了pH、OTC(土霉素)初始质量浓度、H2O2摩尔浓度和催化剂用量对纳米Fe/Co催化剂催化性能的影响,并通过SEM(扫描电子显微镜)和BET(比表面积测试仪)对纳米Fe/Co催化剂进行表征,进一步研究了纳米Fe/Co催化剂对OTC模拟废水的催化降解效果.结果表明:①纳米Fe/Co催化剂可以有效地改善催化体系的pH使用范围,在pH为3.0~11.0范围内,纳米Fe/Co催化剂对浓度为100 mg/L OTC的去除率(94.0%)高于纳米Fe催化剂(85.0%);低浓度OTC有利于提高污染物的去除率,而高浓度的OTC有利于提高反应速率;H2O2摩尔浓度为200 mmol/L时,纳米Fe/Co催化剂对OTC的去除率最高(93.8%);纳米Fe/Co催化剂用量为6 g/L时,其对OTC的去除率最高(92.8%).②纳米Fe/Co催化剂粒径为20~30 nm,比表面积较高,为121.3 m2/g.③纳米Fe/Co催化剂在重复利用13次后OTC去除率仍在50.0%以上,其重复利用性能良好.研究显示,纳米Fe/Co催化剂对OTC废水具有较好的催化性能、重复利用性能以及较宽的pH使用范围,可为含抗生素废水处理提供理论支撑. 相似文献