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651.
天然黄铁矿的除磷性能 总被引:1,自引:0,他引:1
除磷是控制水体富营养化的重要手段。为了考察黄铁矿的除磷特征,采用序批实验,分别研究了反应时间、初始磷浓度和干扰离子(NH4+、NO3- 和SO24-)对黄铁矿除磷的影响。动力学表明,黄铁矿的除磷过程符合伪二级动力学模型。pH=6.5时,磷的平衡去除量为6.82mg/kg。Langmuir方程能较好描述黄铁矿除磷的吸附等温过程,其磷的饱和吸附量为11.01mg/kg。NH4+、NO3-和SO24- 对黄铁矿除磷基本没有影响。磷的去除主要是通过铁磷沉淀和铁氧化物及氢氧化物的吸附,去除的磷主要以可被生物利用的Fe、Al-P形态存在。黄铁矿的这些除磷性能和机制对选取黄铁矿作为人工湿地填料实现同步脱氮除磷具有重要指导作用。 相似文献
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Mercury (Hg) has received considerable attention because of its association with various human health problems. Adsorption-desorption behavior of Hg at contaminated levels in two paddy soils was investigated. The two representative soils for rice production in China, locally referred to as a yellowish red soil (YRS) and silty loam soil (SLS) and classified as Gleyi-Stagnic Anthrosols in FAO/UNESCO nomenclature, were respectively collected from Jiaxin County and Xiasha District of Hangzhou City, Zhejiang Province. The YRS adsorbed more Hg(2+) than the SLS. The characteristics of Hg adsorption could be described by the simple Langmuir adsorption equation (r2 = 0.999 and 0.999, P < 0.01, respectively, for the SLS and YRS). The maximum adsorption values (Xm) that were obtained from the simple Langmuir model were 111 and 213 mg Hg(2+) kg(-1) soil, respectively, for the SLS and YRS. Adsorption of Hg(2+) decreased soil pH by 0.75 unit for the SLS soil and 0.91 unit for the YRS soil at the highest loading. The distribution coefficient (kd) of Hg in the soil decreased exponentially with increasing Hg(2+) loading. After five successive desorptions with 0.01 mol L(-1) KCl solution (pH 5.4), 0 to 24.4% of the total adsorbed Hg(2+) in the SLS soil was desorbed and the corresponding value of the YRS soil was 0 to 14.4%, indicating that the SLS soil had a lower affinity for Hg(2+) than the YRS soil at the same Hg(2+) loading. Different mechanisms are likely involved in Hg(2+) adsorption-desorption at different levels of Hg(2+) loading and between the two soils. 相似文献
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656.
A rapid spectrophotometric determination of persulfate anion in ISCO 总被引:10,自引:0,他引:10
Due to a gradual increase in the use of persulfate as an in situ chemical oxidation (ISCO) oxidant, a simple measurement of persulfate concentration is desirable to analyze persulfate distribution at designated time intervals on/off a site. Such a distribution helps evaluate efficacy of ISCO treatment at a site. This work proposes a spectrophotometric determination of persulfate based on modification of the iodometric titration method. The analysis of absorption spectra of a yellow color solution resulting from the reaction of persulfate and iodide in the presence of sodium bicarbonate reveals an absorbance at 352 nm, without significant interferences from the reagent matrix. The calibration graph was linear in the range of persulfate solution concentration of 0-70 mM at 352 nm. The proposed method is validated by the iodometric titration method. The solution pH was at near neutral and the presence of iron activator does not interfere with the absorption measurement. Also, analysis of persulfate in a groundwater sample using the proposed method indicates a good agreement with measurements by the titration method. This proposed spectrophotometric quantification of persulfate provides a simple and rapid method for evaluation of ISCO effectiveness at a remediation site. 相似文献
657.
In situ iron activated persulfate oxidative fluid sparging treatment of TCE contamination--a proof of concept study 总被引:1,自引:0,他引:1
In situ chemical oxidation (ISCO) is considered a reliable technology to treat groundwater contaminated with high concentrations of organic contaminants. An ISCO oxidant, persulfate anion (S(2)O(8)(2-)) can be activated by ferrous ion (Fe(2+)) to generate sulfate radicals (E(o)=2.6 V), which are capable of destroying trichloroethylene (TCE). The property of polarity inhibits S(2)O(8)(2-) or sulfate radical (SO(4)(-)) from effectively oxidizing separate phase TCE, a dense non-aqueous phase liquid (DNAPL). Thus the oxidation primarily takes place in the aqueous phase where TCE is dissolved. A bench column study was conducted to demonstrate a conceptual remediation method by flushing either S(2)O(8)(2-) or Fe(2+) through a soil column, where the TCE DNAPL was present, and passing the dissolved mixture through either a Fe(2+) or S(2)O(8)(2-) fluid sparging curtain. Also, the effect of a solubility enhancing chemical, hydroxypropyl-beta-cyclodextrin (HPCD), was tested to evaluate its ability to increase the aqueous TCE concentration. Both flushing arrangements may result in similar TCE degradation efficiencies of 35% to 42% estimated by the ratio of TCE degraded/(TCE degraded+TCE remained in effluent) and degradation byproduct chloride generation rates of 4.9 to 7.6 mg Cl(-) per soil column pore volume. The addition of HPCD did greatly increase the aqueous TCE concentration. However, the TCE degradation efficiency decreased because the TCE degradation was a lower percentage of the relatively greater amount of dissolved TCE by HPCD. This conceptual treatment may serve as a reference for potential on-site application. 相似文献
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659.
基于三角模糊数的民航企业“管理”安全综合评价模型研究 总被引:2,自引:0,他引:2
在对我国民航企业安全管理的现状和常用的安全评价方法进行分析的基础上,提出并建立了民航企业"管理"安全模糊综合评价模型。首先,从组织管理、风险管理、安全保证、安全促进4个方面对民航企业安全管理的内容和特点进行分析,在此基础上建立民航企业"管理"安全评价指标体系;然后,根据三角模糊数理论和模糊综合评价理论建立民航企业"管理"安全模糊综合评价模型;通过上述指标体系和评价模型从而达到对民航企业"管理"安全进行评价的目的。最后,给出了一个应用实例,其评价结果表明:该模型具有很强的实用性和借鉴价值。 相似文献
660.
针对地下储库受限空间的特点和油气爆炸抑制的需要.在前期所完成的系统油气爆炸试验和理论研究的基础上,采用超细冷气溶胶抑爆新技术,建立地下受限空间油气爆炸及其抑爆模拟试验系统,研制出新型超细冷气溶胶粉体抑爆剂,并对其进行可行性与有效性研究.对地下受限空间油气爆炸抑制的影响因素进行研究,分析了抑爆剂作用机理.结果表明:超细冷气溶胶是一种高效的抑制地下储库油气爆炸的抑爆剂;在相同试验条件下,迎着火焰传播方向喷射抑爆剂的抑爆效果优于垂直火焰传播方向喷射抑爆剂;喷射压力存在临界值,较小较大都不利于油气爆炸抑制,在本文试验条件下.最佳抑爆效果的喷射压力临界值约为0.8 Mpa;抑爆剂用量不能低于临界抑爆浓度,实验得到的抑爆刑临界浓度为0.232 ks/m3;布置方式对抑爆效果具有明显的影响.分散布置比集中布置具有更好的抑爆效果.本文的研究对后续抑爆装置的研制提供了重要的理论参考和关键设计参数. 相似文献