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In the present study, the distribution patterns of various metals were analyzed and compared using PM samples collected concurrently from three monitoring sites located in Korea (Seoul, Busan, and Jeju island) in December 2002. As these sites can represent metal pollution with different degrees of anthropogenic activities, their concentration levels were distinguished in a systematic manner in the order of Jeju, Busan, and Seoul. By comparing the present data sets with those measured previously from other locations in Korea and around the world, we attempted to diagnose the general status of elemental pollution on the Korean peninsula. Through an application of different statistical approaches, the major processes controlling elemental levels were assessed for each of the three study sites. The results indicated the importance of both crustal and anthropogenic sources in all sites with their relative roles varying significantly from each other. The results of the metal analysis data, when examined in relation to back trajectory analysis, confirmed that their concentration changes are affected quite sensitively with air mass movement patterns. The overall results of this study consistently indicated the contribution of a strong anthropogenic source area (e.g., China) to the observed metal concentration levels in the study area, but the strengths of such signals vary considerably across the Korean peninsula.  相似文献   
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东北亚地区沙尘暴监测合作机制研究   总被引:1,自引:1,他引:0  
近年来,东北亚各国重视沙尘暴问题,开展了沙尘暴监测及研究等合作,逐步建立起东北亚地区沙尘暴监测合作机制.合作机制对推动东北亚地区共同治理沙尘暴问题具有积极意义.文章通过分析东北亚主要国家中国、日本和韩国的沙尘暴监测机制,探讨沙尘暴监测的合作机制模式,进而分析合作机制对推动各国在监测方法、管理机制等方面的促进作用.  相似文献   
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戴亮  赵伟繁  张洪伟  韩涛  张康 《环境工程》2020,38(12):70-77
重金属带来的环境风险日益严峻,利用污泥生物炭去除水中重金属污染方面的研究得到了广泛关注。结合当前国内外研究现状,归纳了不同条件下制备的污泥生物炭对水中重金属,如Cd、Pb、Cr、As等的吸附机理,污泥生物炭对大多数重金属的吸附满足物理吸附和化学吸附的多重作用,可通过增加生物炭表面有效基团及有效吸附位点提升吸附性能。同时,总结了影响吸附效率的各种因素,探究了污泥生物炭的再生问题,并对今后污泥生物炭去除水中重金属的研究方向做出了展望。  相似文献   
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To clarify the aerosol hygroscopic growth and optical properties of the Pearl River Delta(PRD)region,integrated observations were conducted in Heshan City of Guangdong Province from October 19 to November 17,2014.The concentrations and chemical compositions of PM_(2.5),aerosol optical properties and meteorological parameters were measured.The mean value of PM_(2.5) increased from less than 35(excellent) to 35-75 μg/m~3(good) and then to greater than 75 μg/m~3(pollution),corresponding to mean PM_(2.5) values of 24.9,51.2,and 93.3 μg/m~3,respectively.The aerosol scattering hygroscopic growth factor(f(RH = 80%)) values were 2.0,2.12,and 2.18 for the excellent,good,and pollution levels,respectively.The atmospheric extinction coefficient(σext)and the absorption coefficient of aerosols(σ_(ap)) increased,and the single scattering albedo(SSA)decreased from the excellent to the pollution levels.For different air mass sources,under excellent and good levels,the land air mass from northern Heshan had lower f(RH) and σ_(sp) values.In addition,the mixed aerosol from the sea and coastal cities had lower f(RH) and showed that the local sources of coastal cities have higher scattering characteristics in pollution periods.  相似文献   
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CuSO_4/TiO_2 catalysts with high catalytic activity and excellent resistant to SO_2 and H_2 O,were thought to be promising catalysts used in Selective catalytic reduction of nitrogen oxides by NH_3.The performance of catalysts is largely affected by calcination temperature.Here,effects of calcination temperature on physicochemical property and catalytic activity of CuSO_4/TiO_2 catalysts were investigated in depth.Catalyst samples calcined at different temperatures were prepared first and then physicochemical properties of the catalyst were characterized by N2 adsorption-desorption,X-ray diffraction,thermogravimetric analysis,Raman spectra,Fourier-transform infrared spectroscopy,X-ray photoelectron spectroscopy,temperature-pro grammed desorption of NH_3,temperature-programmed reduction of H_2 and in situ diffuse reflectance infrared Fourier transform spectroscopy.Results revealed that high calcination temperature had three main effects on the catalyst.First,sintering and anatase transform into rutile with increase of calcination temperature,causing a decrement of specific surface area.Second,decomposition of CuSO_4 under higher calcination temperature,resulting in disappears of Br(?)nsted acid sites(S-OH),which had an adverse effect on surface acidity.Third,CuO from the decomposition of CuSO_4 changed surface reducibility of the catalyst and favored the process of NH_3 oxidation to nitrogen oxides(NO_x).Thus,catalytic activity of the catalyst calcined under high temperatures(≥600℃) decreased largely.  相似文献   
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Molecular level characterization of dissolved organic sulfur (DOS) by electrospray ionization-Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICR MS) is necessary for further understanding of the role of DOS in the environment. Here, ESI spray solvent, a key parameter for ion production during ESI process, was investigated for its effect on the molecular characterization of DOS by ESI-FTICR MS. 100% MeOH as spray solvent was found for the first time to remarkably enhance the ionization efficiency of the majority of CHOS-molecules in NOM, which facilitated a total of 1473 CHOS-molecular formulas with one sulfur atom to be detected. The number of CHOS-molecular formulas obtained using 100%MeOH as spray solvent increased notably over 740 in comparison with those using 50% MeOH aqueous solution (731) or 50% ACN aqueous solution (653). Moreover, due to the enhancement of ionization efficiency of DOS during ESI processes, the tandem mass spectra of the NOM CHOS-molecules could be easily obtained using 100% MeOH as spray solvent, which were hardly obtained using 50% MeOH aqueous solution as spray solvent. The results of the tandem mass spectra suggested the first discovery of organosulfates or sulfonic acids in Suwannee River NOM sample. A simple method based on 100% MeOH as ESI spray solvent for advanced molecular characterization of DOS by ESI-FTICR MS was proposed and applied, and the results revealed more molecular information of DOS in sea DOM samples.  相似文献   
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为了促进污水处理厂剩余污泥的资源化利用,探索S-HA(sludge-based humic acid, 污泥腐殖酸)对溶液中重金属Cd2+的吸附特性.采用国际腐殖酸协会(IHSS)推荐的方法提取S-HA,通过元素分析、FT-IR(傅里叶红外光谱分析)和SEM-EDS(外观形态分析)等方法,考察溶液pH和共存阳离子对吸附过程的影响,并对吸附过程分别进行了吸附动力学模型、等温吸附模型和吸附热力学模型拟合,同时通过对比S-HA吸附前后的红外光谱和扫描电镜-能谱图片,探索S-HA对Cd2+的吸附机制.结果表明:①S-HA表面呈松散的簇团状,含有大量的羧基、醇羟基和酚羟基等含氧官能团,芳香度较高,含有较多的脂肪链结构;S-HA在吸附水中Cd2+的过程中,Cd2+与S-HA表面上的酚羟基、羧基等官能团发生了络合作用.②S-HA对Cd2+的吸附量随溶液pH升高而增加,溶液中Na+、NH4+和Ca2+等共存阳离子的存在不利于S-HA对Cd2+的吸附,其中Ca2+的存在对S-HA吸附Cd2+影响最大.③S-HA对Cd2+的吸附由快吸附、慢吸附和吸附平衡3个阶段组成,吸附平衡时间为12 h;吸附过程符合准二级动力学模型,其整体吸附速度由液膜扩散和颗粒内扩散共同控制;吸附等温线符合Freundlich等温吸附模型,25℃下的最大吸附量为19.29 mg/g,Cd2+在S-HA上的吸附是自发吸热反应.研究显示:污水处理厂剩余污泥提取的S-HA对Cd2+具有较好的吸附效果;S-HA对Cd2+的吸附过程同时存在着物理吸附和化学吸附;高pH对S-HA吸附Cd2+有促进作用,而高离子强度对S-HA吸附Cd2+有抑制作用.   相似文献   
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为探究半干旱区地表水化学特征及物质来源,以白洋淀流域为研究对象,利用Piper三线图和Gibbs水岩模型,对地表水的主要离子组成特征及其来源进行分析。结果表明:白洋淀流域地表水pH为7.56~8.23时,呈弱碱性,且溶解性总固体(TDS,100~650 mg/L)在流域的不同空间区域表现为淀区 > 下游 > 上游。白洋淀流域地表水阳离子以Na+和Ca2+为主,离子总量占比76.60%;阴离子以HCO3-为主,约占阴离子总量61.52%。地表水的水化学类型为HCO3-Ca型(上游水体)和HCO3·SO4·Cl-Na·Ca型(下游河流和淀区)。白洋淀水文地球化学过程受到人类活动和自然作用的双重控制;自然作用下,白洋淀流域地表水中的离子来源于岩石风化(碳酸盐岩及硅酸盐岩的风化溶解),同时受到蒸发-结晶作用影响。  相似文献   
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