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排序方式: 共有128条查询结果,搜索用时 250 毫秒
1.
Ji Hu Jianmin Wang Shuxia Liu Zhechao Zhang Haifeng Zhang Xiaoxia Cai Jianming Pan Jingjing Liu 《环境科学学报(英文版)》2018,30(4):208-215
TiO_2 nanoparticles(NPs) could adversely impact aquatic ecosystems. However, the aggregation of these NPs could attenuate this effect. In this work, the biological effects of TiO_2 NPs on a marine microalgae Isochrysis galbana were investigated. The aggregation kinetics of TiO_2 NPs under different conditions was also investigated to determine and understand these effects. Results showed that, though TiO_2 NPs had no obvious impact on the size and reproducibility of algal cells under testing conditions, they caused a negative effect on algal chlorophyll, which led to a reduction in photosynthesis. Furthermore, fast aggregation of TiO_2 NPs occurred under all conditions, especially at the pH close to the p Hzpc. Increasing ionic strength and NP concentration also enhanced the aggregation rate.The aggregation and the following sedimentation of TiO_2 NPs reduced their adverse effects on I. galbana. 相似文献
2.
硫酸法钛白生产水洗工序清洁生产技术初探 总被引:1,自引:0,他引:1
通过开展水洗工段用水审计并试验了温度、偏钛酸ξ电位和漂白工艺对水洗的影响效果,从实践和理论上探讨了为其提高钛白质量改进水洗工艺的清洁生产方案的可行性和合理性。 相似文献
3.
TiO2膜固载型多孔催化剂的光催化分解试验 总被引:3,自引:0,他引:3
以多孔基质为载体,用溶胶-凝胶法制备出载TiO2薄膜的多孔型光催化剂。用X射线衍射和扫描电镜对催化剂的物相和形貌进行了表征,此催化剂能在光照下分解水溶液中四环素抗菌素。经1h光照,四环素的分解率可达85%左右。 相似文献
4.
5.
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
6.
4—氯苯甲酸钠的光催化氧化降解及其影响因素 总被引:8,自引:0,他引:8
本试验采用P-25TiO2,光催化剂,对4-氯苯甲酸钠的光催化氧化降解及污染物初始浓度,催化剂投加量和入射光强等因素的影响进行了研究,研究发现污染物初始降解速率与其初始浓度的关系遵循Langmuir-Hinshelwood模式,其中半饱和浓度常数Ks不仅是催化剂和污染物种类的函数,而且也是入射光强的函数,催化剂投加量存在一限值,当低于此限值时,污染物降解速率由于催化剂浓度的不足受到影响而下降,当高于此限值时,污染物降解速率受催化剂投加量的影响变小,在本试验4-CBA-Na浓度为0.15-0.6mmol/L时该催化剂限值浓度大约为0.4g/L,在入射光强为1-7mW/cm^2和催化剂浓度为0.4g/L下,污染物降解速率与光强成0.67次幂关系,经估算其量子效率为6.3%。 相似文献
7.
Botta C Labille J Auffan M Borschneck D Miche H Cabié M Masion A Rose J Bottero JY 《Environmental pollution (Barking, Essex : 1987)》2011,159(6):1543-1550
This work investigates the physical-chemical evolution during artificial aging in water of four commercialized sunscreens containing TiO2-based nanocomposites. Sunscreens were analyzed in terms of mineralogy and TiO2 concentration. The residues formed after aging were characterized in size, shape, chemistry and surface properties. The results showed that a significant fraction of nano-TiO2 residues was released from all sunscreens, despite their heterogeneous behaviors. A stable dispersion of submicronic aggregates of nanoparticles was generated, representing up to 38 w/w% of the amount of sunscreen, and containing up to 30% of the total nano-TiO2 initially present in the creams. The stability of the dispersion was tested as a function of salt concentration, revealing that in seawater conditions, a major part of these nano-TiO2 residues will aggregate and sediment. These results were put in perspective with consumption and life cycle of sunscreens to estimate the amount of nano-TiO2 potentially released into AQUATIC environment. 相似文献
8.
Justin M. Langridge R. Joel Gustafsson Paul T. Griffiths R. Anthony Cox Richard M. Lambert Roderic L. Jones 《Atmospheric environment (Oxford, England : 1994)》2009,43(32):5128-5131
The photoenhanced uptake of nitrogen dioxide (NO2) to the surface of commercially available self-cleaning window glass has been studied under controlled laboratory conditions. This material is one of an array of modern building products which incorporate titanium dioxide (TiO2) nanoparticles and are finding increasing use in populated urban areas. Amongst the principal drivers for the use of these materials is that they are thought to facilitate the irreversible removal of pollutants such as NO2 and organic molecules from the atmosphere and thus act to remediate air quality. While it appears that TiO2 materials do indeed remove organic molecules from built environments, in this study we show that the photoenhanced uptake of NO2 to one example material, self-cleaning window glass, is in fact accompanied by the substantial formation (50–70%) of gaseous nitrous acid (HONO). This finding has direct and serious implications for the use of these materials in urban areas. Not only is HONO a harmful respiratory irritant, it is also readily photolysed by solar radiation leading to the formation of hydroxyl radicals (OH) together with the re-release of NOx as NO. The net effect of subsequent OH initiated chemistry can then be the further degradation of air quality through the formation of secondary pollutants such as ozone and VOC oxidation products. In summary, we suggest that a scientifically conceived technical strategy for air quality remediation based on this technology, while widely perceived as universally beneficial, could in fact have effects precisely opposite to those intended. 相似文献
9.
The photocatalytic degradation of a dye derivative, C.I. disperse blue 1 (1), has been investigated under UV light irradiation in the presence of TiO2 and H2O2 under a variety of conditions. The degradation was studied by monitoring the change in substrate concentration employing UV spectroscopic technique as a function of irradiation time. The degradation was studied under different conditions such as different types of TiO2, reaction pH, catalyst and substrate concentration containing hydrogen peroxide (H2O2), besides molecular oxygen in the presence of TiO2. The degradation of dye was also investigated under sunlight and the efficiency of degradation was compared with that of the artificial light source. The degradation rates were found to be strongly influenced by all the above parameters. The photocatalyst Degussa P25 was found to be more efficient for the degradation of the dye. 相似文献
10.