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151.
pH和共存阳离子对草莓茎吸附水体氨氮的影响 总被引:6,自引:4,他引:2
为了开发新型氨氮吸附剂和探讨环境因素对氨氮吸附的影响,以草莓茎为吸附材料,通过批平衡法研究了不同初始pH、共存阳离子、初始浓度和温度下氨氮去除的特点.结果表明,等温吸附符合Langmuir和Freundlich这2种模型,理论最大吸附量qm在15、25和35℃下分别为3.05、4.24和4.79 mg.g-1.温度升高有利于草莓茎对氨氮的吸附.草莓茎吸附氨氮最适初始pH为4~8.低pH减少草莓茎表面负电荷,高pH减少溶液中NH 4+的含量,都减少氨氮的吸附.草莓茎对溶液pH的缓冲则缓和了两者对氨氮吸附的影响.共存阳离子K+、Na+、Ca2+、Mg2+对草莓吸附铵离子没有竞争作用,而Zn2+、Al3+则由于其水解降低溶液的pH而显著降低草莓茎对氨氮的吸附.草莓茎吸附氨氮的应用pH范围较广且不易受废水中常见金属阳离子的干扰,说明草莓茎不仅可以作为废水中氨氮的吸附剂原料,而且较大多数矿物原料还有其自身的优势. 相似文献
152.
次氯酸钠氧化消除水中BPA的影响因素和动力学 总被引:1,自引:0,他引:1
采用常用消毒剂次氯酸钠对内分泌干扰物双酚A(BPA)的氧化消除及动力学规律进行研究,考察了加氯量、BPA初始浓度、pH值、Br-浓度和温度各因素对降解效果的影响.结果表明,次氯酸钠对BPA的氧化降解过程符合拟一级反应动力学;pH值对该降解反应影响较大,当pH为8~9时,BPA与 HOCl的反应速率达到最大为0 .544 3 min-1;溶液中存在Br-会加快BPA的降解,并且其整体反应不符合拟一级动力学规律,随着Br-浓度的增加,BPA降解得越快;温度对该降解反应的影响较大并且符合Van't Hoff规则,提高反应温度,有利于氯对BPA的降解. 相似文献
153.
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
154.
155.
156.
为了解北京城区大气干沉降中水溶性离子的化学组成与时间变化特征,连续进行了4年多的干沉降采样与分析.结果表明,在222个有效干沉降样品中,存在不同程度的阴离子缺失. SO42-与Ca2+分别是含量最丰富的阴、阳离子组分,其次是NO3-和NH4+. SO42-、NO3-和NH4+呈现相似的季节变化特征,即其浓度在夏季最高,冬季最低. 干沉降基本呈中性,其pH值月变化幅度小,但季节变化明显,夏季低而春季高. 相似文献
157.
文章介绍了生物可利用态的磷(总磷、有机磷、无机磷)在土耳其奥龙特斯河河水和表层沉积物中的分配结果.通过连续提取方法可获得无机态的磷,每次获得的无机磷有4种形态:松散吸附态的磷、铝绑定态磷、铁绑定态磷 相似文献
158.
Yanhui Li Bing Xi Quansheng Zhao Fuqiang Liu Pan Zhang Qiuju Du Dechang Wang Da Li Zonghua Wang Yanzhi Xia 《环境科学学报(英文版)》2011,23(3):404-411
Kaolin has been widely used as an adsorbent to remove heavy metal ions from aqueous solutions. However, the lower heavy metal
adsorption capacity of kaolin limits its practical application. A novel environmental friendly material, calcium alginate immobilized
kaolin (kaolin/CA), was prepared using a sol-gel method. The e ects of contact time, pH, adsorbent dose, and temperature on Cu2+
adsorption by kaolin/CA were investigated. The Langmuir isotherm was used to describe the experimental adsorption, the maximum
Cu2+ adsorption capacity of the kaolin/CA reached up to 53.63 mg/g. The thermodynamic studies showed that the adsorption reaction
was a spontaneous and endothermic process. 相似文献
159.
Yusheng Wang Zhiguo Pei Xiaoquan Shan Guangcai Chen Jing Zhang Yaning Xie Lirong Zheng 《环境科学学报(英文版)》2011,23(1):112-118
The mutual e ects of metal cations (Cu2+, Pb2+, Zn2+, and Cd2+) and p-nitrophenol (NP) on their adsorption desorption behavior
onto wheat ash were studied. Results suggested that Cu2+, Pb2+, and Zn2+ diminished the adsorption and increased the desorption of
NP remarkably, while Cd2+ had no such e ect. In contrast, NP diminished the adsorption of Cu2+, Pb2+, and Zn2+ onto ash, however,
this suppression e ect depended on the initial concentrations of metal cations. NP had no e ect on Cd2+ adsorption on ash. Fourier
transform infrared (FT-IR) and X-ray absorption spectroscopic (XAS) studies suggested the following mechanisms responsible for the
metal suppression e ect on NP adsorption: (1) large hydrated Cu2+, Pb2+, and Zn2+ shells occupied the surface of ash and prevent
nonspecific adsorption of NP onto ash surface; (2) Cu2+, Pb2+, and Zn2+ may block the micropores of ash, resulting in decreased
adsorption of NP; (3) complexation of Cu2+, Pb2+, and Zn2+ was likely via carboxyl, hydroxylic and phenolic groups of wheat ash and
these same groups may also react with NP during adsorption. As a “soft acid”, Cd2+ is less e cient in the complexation of oxygencontaining
acid groups than Cu2+, Pb2+, and Zn2+. Thus, Cd2+ had no e ect on the adsorption of NP on wheat ash. 相似文献
160.
Seepage from Hg mine wastes and calcines contains high concentrations of mercury (Hg). Hg pollution is a major environmental
problem in areas with abandoned mercury mines and retorting units. This study evaluates factors, especially the hydrological and
sedimentary variables, governing temporal and spatial variation in levels and state of mercury in streams impacted by Hg contaminated
runo . Samples were taken during di erent flow regimes in theWanshan Hg mining area in Guizhou Province, China. In its headwaters
the sampled streams/rivers pass by several mine wastes and calcines with high concentration of Hg. Seepage causes serious Hg
contamination to the downstream area. Concentrations of Hg in water samples showed significant seasonal variations. Periods of
higher flow showed high concentrations of total Hg (THg) in water due to more particles being re-suspended and transported. The
concentrations of major anions (e.g., Cl??, F??, NO3?? and SO4
2??) were lower during higher flow due to dilution. Due to both sedimentation
of particles and dilution from tributaries the concentration of THg decreased from 2100 ng/L to background levels (< 50 ng/L) within
10 km distance downstream. Sedimentation is the main reason for the fast decrease of the concentration, it accounts for 69% and 60%
for higher flow and lower flow regimes respectively in the upper part of the stream. Speciation calculation of the dissolved Hg fraction
(DHg) (using Visual MINTEQ) showed that Hg(OH)2 associated with dissolved organic matter is the main form of Hg in dissolved
phase in surface waters in Wanshan (over 95%). 相似文献