全文获取类型
收费全文 | 69篇 |
免费 | 4篇 |
国内免费 | 25篇 |
专业分类
安全科学 | 2篇 |
废物处理 | 3篇 |
环保管理 | 5篇 |
综合类 | 35篇 |
基础理论 | 28篇 |
污染及防治 | 13篇 |
评价与监测 | 12篇 |
出版年
2021年 | 2篇 |
2020年 | 3篇 |
2019年 | 1篇 |
2018年 | 2篇 |
2017年 | 2篇 |
2016年 | 1篇 |
2015年 | 4篇 |
2014年 | 3篇 |
2013年 | 19篇 |
2012年 | 8篇 |
2011年 | 6篇 |
2010年 | 2篇 |
2009年 | 4篇 |
2008年 | 5篇 |
2007年 | 6篇 |
2006年 | 4篇 |
2005年 | 5篇 |
2004年 | 2篇 |
2003年 | 4篇 |
2002年 | 1篇 |
2001年 | 2篇 |
2000年 | 1篇 |
1999年 | 1篇 |
1998年 | 2篇 |
1997年 | 1篇 |
1996年 | 2篇 |
1994年 | 2篇 |
1993年 | 1篇 |
1989年 | 1篇 |
1987年 | 1篇 |
排序方式: 共有98条查询结果,搜索用时 31 毫秒
61.
Liviana Leita Alja Margon Iztok Ar?on Marco Contin 《Environmental pollution (Barking, Essex : 1987)》2009,157(6):1862-1866
The interaction between hexavalent chromium Cr(VI), as K2CrO4, and standard humic acids (HAs) in bulk solution was studied using three complementary analytical methods: UV-Visible spectroscopy, X-ray absorption spectroscopy and differential pulse stripping voltammetry. The observed UV-Vis and X-ray absorption spectra showed that, under our experimental conditions, HAs did not induce reduction of Cr(VI) to its trivalent chemical form. The interaction between Cr(VI) and HAs has rather led to the formation of Cr(VI)-HAs micelles via supramolecular chemical processes. The reported results could contribute towards explaining the relative persistence of ecotoxic hexavalent chromium in soils. 相似文献
62.
A novel differential pulse voltammetry (DPV) method was developed for the simultaneous analysis of herbicides in water. A mixture of four herbicides, atrazine, simazine, propazine and terbuthylazine was analyzed simultaneously and the complex, overlapping DPV voltammograms were resolved by several chemometrics methods such as partial least squares (PLS), principal component regression (PCR) and principal component–artificial networks (PC–ANN). The complex profiles of the voltammograms collected from a synthetic set of samples were best resolved with the use of the PC–ANN method, and the best predictions of the concentrations of the analytes were obtained with the PC-ANN model (%RPET = 6.1 and average %Recovery = 99.0). The new method was also used for analysis of real samples, and the obtained results were compared well with those from the GC-MS technique. Such conclusions suggest that the novel method is a viable alternative to the other commonly used methods such as GC, HPLC and GC-MS. 相似文献
63.
磷钼杂多阴离子薄膜修饰电极伏安法测定造纸黑液中的磷 总被引:3,自引:0,他引:3
本文报导了用磷钼杂多阴离子薄膜修饰电极伏安法测定造纸黑液中的磷,试样以HClO4煮沸5min,排除硅和有机物的干扰。磷浓度在0.04-10mg·^-1范围内与峰电流呈良好线性关系。 相似文献
64.
Arsenic(III), selenium(IV), copper(II), lead(II), cadmium(II),zinc(II) have been determined in sea water, sediments, algae andclams by differential pulse cathodic (DPCSV) and anodic (DPASV)stripping voltammetry. The voltammetric measurements are carriedout using a conventional three-electrode cell and the ammonia-ammonium chloride buffer pH 9.2 as supporting electrolyte.The analytical procedure has been verified by the analysisof the standard reference materials (Estuarine SedimentBCR-CRM 277, Ulva Lactuca BCR-CRM 279 and Mussel Tissue BCR-CRM278). The precision and the accuracy are less than 5%. Thisprocedure is utilized for the monitoring of heavy metals inthe Po river mouth area (Italy). 相似文献
65.
阳极溶出伏安法连续测定底泥中的总镉和总铅 总被引:1,自引:0,他引:1
样品经盐酸-硝酸-氢氟酸-高氯酸消解后,用1+1盐酸溶解残渣,以高氯酸做支持电解质,采用阳极溶出伏安法的标准加入法,测定样品中的总镉和总铅,取得满意结果。 相似文献
66.
Voltammetric response of ferroceneboronic acid to diol and phenolic
compounds as possible pollutants
Shigehiro Takahashi Naoyuki Abiko Nobuhiro Haraguchi Hiroyuki Fujit Eriko Seki Tetsuya Ono Kentaro Yoshi Jun-ichi Anzai 《环境科学学报(英文版)》2011,23(6):1027-1032
A voltammetric determination of possible organic pollutants such as diol and phenolic compounds in water was studied using
ferroceneboronic acid (FBA) as a redox-active marker. A cyclic voltammogram of FBA exhibited a pair of oxidation and reduction
peaks at 230 and 170 mV at pH 7.0, respectively, while another pair of redox peaks was observed in the presence of diol or phenolic
compounds tested. The results were rationalized based on the formation of boronate esters of FBA with the added compounds. The
changes in the redox peak currents were dependent on the concentration of the additives, suggesting a usefulness of FBA in the
electrochemical determination of these compounds in water. 相似文献
67.
制备嵌入式多壁碳纳米管修饰石墨电极(ESCFE),利用循环伏安法研究铅(Pb)的电化学行为及反应机理,结果表明,铅在修饰电极表面出现了一对明显的准可逆的氧化还原峰,发生了2质子的电化学氧化反应。用差分脉冲伏安法研究了铅离子浓度与其峰电流的线性关系,线性范围为1.8×10^-7~1.0×10^-5g/L,线性方程为:ipa(μA)=0.12+1.471c×10^6(g/L),r=0.9999,检出限为6.0×10^-8g/L,RSD%为1.015(n=5)。利用本法对湖泊沉积物中铅进行测定,样品铅含量:0.218~0.6317mg/kg,RSD:3.3%~6.2%,加标回收率:94.3%-106.6%。 相似文献
68.
69.
As an effort to better utilize the microbial fuel cell (MFC) technology, we previously proposed an innovative MFC system named M2FC consisting of ferric-based MFC part and ferrous-based fuel cell (FC) part. In this reactor, ferric ion, the catholyte in the MFC part, was efficiently regenerated by the FC part with the generation of additional electricity. When both units were operated separately, the ferric-based MFC part produced approximately 1360 mW m−2 of power density with FeCl3 as catholyte and Fe-citrate as anolyte. The ferrous-based FC part with FeCl3 as catholyte and Fe-EDTA as anolyte displayed the highest power density (1500 mW m−2), while that with ferricyanide as catholyte and Fe-noligand as anolyte had the lowest power density (380 mW m−2). The types of catholytes and chelating complexes as anolyte were found to play important roles in the reduction of ferric ions and oxidation of ferrous ion. Linear sweep voltammetry results supported that the cathode electrolytes were electrically active and these agreed well with the M2FC reactor performance. These results clearly showed that ligands played critical role in the efficiency and rate for recycling iron ion and thus the M2FC performance. 相似文献
70.
Thriveni T Rajesh Kumar J Sujatha D Sreedhar NY 《Environmental monitoring and assessment》2007,128(1-3):359-368
The cyclic voltammograms of terbacil and lenacil at the hanging mercury drop electrode showed a single well defined four electron
irreversible peak in universal buffer of pH 4.0 for both compounds. The peak potentials were shifted to more negative values
on the increase of pH of the medium, implying the involvement of protons in the electrode reaction and that the proton transfer
reaction precedes the proper electrode process. The four electron single peak may be attributed to the simultaneous reduction
of carbonyl groups present in 2 and 4 in pyrimidine ring of terbacil and lenacil to the corresponding hydroxy derivative.
Based on the interfacial adsorptive character of the terbacil and lenacil onto the mercury electrode surface, a simple sensitive
and low cost differential pulse adsorptive stripping voltammetric procedure was optimized for the analysis of terbacil and
lenacil. The optimal operational conditions of the proposed procedure were accumulation potential E
acc = −0.4 V, accumulation time t
acc = 80 s, scan rate = 40 mV s−1, pulse amplitude = 25 mV using a universal buffer pH 4.0 as a supporting electrolyte. The linear concentration range was
found to be 1.5 × 10−5 to 1.2 × 10−9 mol/l and 1.5 × 10−5 to 2.5 × 10−8 mol/l with the lower detection limit of 1.22 × 10−9 and 2.0 × 10−8 mol/l. The correlation coefficient and relative standard deviation values are found to be 0.942, 0.996, 1.64% and 1.23%,
respectively, for 10 replicants. The procedure was successfully applied for determination of terbacil and lenacil in formulations,
mixed formulations, environmental samples such as fruit samples and spiked water samples. 相似文献