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101.
利用无机溶胶-凝胶技术制备了V2O5-(TiO2)x离子存储电极薄膜。采用X射线衍射(XRD)、原子力显微镜(AFM)、Raman光谱、循环伏安法(CV)和紫外-可见光透射光谱分别研究了复合薄膜的微观结构、化学计量、锂离子注入性能以及光学性能。结果表明复合薄膜具有V2O5的层状结构,其c轴方向的结构取向性有所降低;颗粒尺寸和表面粗糙度显著减小;同时TiO2的复合导致薄膜中V2O5的化学计量发生偏移,氧空位数量增多。当x=0.2时,薄膜具有相对较高的离子存储容量及循环稳定性,并且在离子注入/脱出状态均获得相当高的可见光透过性。 相似文献
102.
海河沉积物对菲的吸附解吸行为研究 总被引:2,自引:0,他引:2
采用北运河坝河断面、海河干流邓善沽断面及葛沽镇断面表层沉积物及南开花园土为吸附剂,以菲为吸附质进行一系列吸附动力学和吸附-解吸平衡实验研究。结果表明,菲在各颗粒物上的吸附动力学过程,在0-4h内基本可达吸附平衡,刚开始吸附速率很快,然后迅速降低,并逐渐稳定;菲在各颗粒物上的等温平衡吸附可用线性等温线方程及Freundlich方程较好的拟合;不同来源颗粒物对菲的吸附能力随颗粒物中有机质含量增加而增强;葛沽镇颗粒物经高温灼烧处理后,其吸附能力明显降低;各天然颗粒物及不同温度灼烧处理的颗粒物对菲的解吸行为存在不同程度的滞后,灼烧颗粒物的滞后性远远大于原颗粒物,颗粒物中的有机质组分及性质对菲的解吸滞后有重要影响 相似文献
103.
酿酒酵母吸附Pb(Ⅱ)的表面特性研究 总被引:1,自引:1,他引:0
为深入探讨酿酒酵母吸附Pb(Ⅱ)的微观作用机制,本文利用表面显微分析技术(SEM-EDS、TEM-EDS、AFM)研究了酿酒酵母细胞吸附重金属离子Pb(Ⅱ)前后的细胞表面变化.研究结果表明,酿酒酵母细胞与Pb(Ⅱ)作用后,细胞表面除吸附Pb(Ⅱ)外,同时产生大量更高浓度的含Pb(Ⅱ)沉淀,导致Pb(Ⅱ)从溶液中被去除.酵母与Pb(Ⅱ)反应前,酵母细胞表面可检测到的主要元素包括C、O、N、P、S、K、Mg;酵母与Pb(Ⅱ)作用后,细胞表面始终保持C、O、P吸收峰,而N、K、Mg、S吸收峰随反应条件不同而减弱、消失或增强.P作为细胞表面组分可能与Pb(Ⅱ)结合.酵母与Pb(Ⅱ)作用过程中,重金属离子促进酵母细胞释放细胞内含物.原子力显微镜(AFM)证实,云母片表面对酵母吸附Pb(Ⅱ)后细胞的铺展变形作用明显增大. 相似文献
104.
105.
The competition between submersed plants has been recognized as an important factor influencing the structure of plant communities
in shallow lakes. The ability of different species to take up and store nutrients from the surrounding ambience varies, and hence plant
community structure might be expected to affect the cycling of nutrients in lake ecosystems. In this study, the uptake of phosphorus
by Hydrilla verticillata and Vallisneria natans was studied and compared in monoculture and competitive mixed-culture plantings.
Results showed that for both studied species the phosphorus concentrations of different tissues and of whole plants was unaffected by
competition. However, the quantity of phosphorus accumulated by whole plants of H. verticillata was significantly higher in mixture
culture than in monoculture, while that of V. natans was lower in the mixed culture. The results indicated that H. verticillata has a
competitive advantage over V. natans, when the two species are grown in competition, and is able to accumulate a greater quantity of
phosphorus. 相似文献
106.
Tao Zhang Qiucheng Li Lili Ding Hongqiang Ren Ke Xu Yonggang Wu Dong Sheng 《环境科学学报(英文版)》2011,23(6):881-890
Chemical precipitation to form magnesium ammonium phosphate (MAP) is an effective technology for recovering ammonium
nitrogen (NH4
+-N). In the present research, we investigated the thermodynamic modeling of the PHREEQC program for NH4
+-N
recovery to evaluate the effect of reaction factors on MAP precipitation. The case study of NH4
+-N recovery from coking wastewater
was conducted to provide a comparison. Response surface methodology (RSM) was applied to assist in understanding the relative
significance of reaction factors and the interactive effects of solution conditions. Thermodynamic modeling indicated that the saturation
index (SI) of MAP followed a polynomial function of pH. The SI of MAP increased logarithmically with the Mg2+/NH4
+ molar ratio
(Mg/N) and the initial NH4
+-N concentration (CN), respectively, while it decreased with an increase in Ca2+/NH4
+ and CO3
2??/NH4
+
molar ratios (Ca/N and CO3
2??/N), respectively. The trends for NH4
+-N removal at different pH and Mg/N levels were similar to the
thermodynamic modeling predictions. The RSM analysis indicated that the factors including pH, Mg/N, CN, Ca/N, (Mg/N) (CO3
2??/N),
(pH)2, (Mg/N)2, and (CN)2 were significant. Response surface plots were useful for understanding the interaction effects on NH4
+-N
recovery. 相似文献
107.
Potassium-modified ceria-zirconia catalyst was synthesized by wetness impregnation method. The ageing treatment was performed in static air at 800℃ for 20 hr to evaluate the thermal stability of the catalyst. The catalysts were characterized by X-ray diffraction,BET surface area, oxygen storage capacity, NOx-temperature programmed desorption and soot-temperature programmed oxidation measurements. By introduction of potassium, the maximum soot oxidation rate temperature (Tm) of the ceria-zirconia based catalyst decreased from 525 to 428℃ in the presence of NO under a loose contact mode. The shift of Tm of the K-modified catalyst after ageing is only 15℃. The enhanced activity of the aged catalyst mainly lies in the promotional effect of potassium on the NOx/oxygen storage cacity as well as the soot-catalyst contact. 相似文献
108.
109.
110.