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61.
62.
广州市天地空一体化环境空气质量监测网络的建设 总被引:1,自引:0,他引:1
简述了原有广州市环境空气自动监测网络情况,通过对环境空气自动监测网络的集成优化,增设站点、扩展监测项目和引入新技术,建立了一个"金字塔形"的集天地空一体化的环境空气监测网络,弥补了原有监测网络在反映环境空气质量总体水平、污染来源解析、预报预警所需的环境质量信息、对环境空气质量的评估等方面的不足,该网络已成功应用于广州亚运会的空气质量保障。 相似文献
63.
用离子色谱法测定环境空气中低浓度氯化氢,是通过测定氯离子质量浓度间接测定氯化氢的质量浓度,测定过程极易受外来氯离子的干扰,使空白值偏高。通过试验确定测定过程中可能存在氯离子干扰的环节,并采取一系列方法消除前期准备、采样和分析全过程中的干扰,以降低空白值。 相似文献
64.
Tong Chen Xiaodong Li Jianhua Yan Shengyong Lu Kefa Cen 《Atmospheric environment (Oxford, England : 1994)》2011,45(36):6567-6575
Levels of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) were determined in fourteen ambient air samples collected in twelve cities of five provinces and one large municipality in China. The PCDD/F concentrations varied from 2.6 to 120 pg m−3 (or from 0.04 to 1.93 pg I-TEQ m−3). Generally, TCDF was the dominant homologue group and as a rule the homologue concentration of PCDF decreased with rising chlorine substitution number of PCDF. In all cases 2,3,4,7,8-PeCDF was the most important contributor to the I-TEQ value, accounting for 35–57% of the total I-TEQ value. Higher PCDD/F levels in ambient air were found during winter. The highest PCDD/F levels were found in Chengdu, Sichuan Province. In general, the PCDD/F levels in this study were in the same range as in other studies in China. 相似文献
65.
The Connecticut Department of Environmental Protection (CTDEP) commenced monitoring for PCDDs/PCDFs (polychlorinated dibenzodioxins and polychlorinated dibenzofurans) in ambient air in 1987 and adopted the long term (30 d) sampling approach in 1993. The CTDEP method represents the first use of isotopically labeled PCDDs/PCDFs as field surrogates to monitor the behavior of native PCDDs/PCDFs present in actual ambient air samples. This feature first introduced in 1987 was later adopted by US EPA in revisions to sampling methods for PCDDs/PCDFs in ambient air (EPA Method TO9A) as well as development of EPA Reference Method 23 for measurement of PCDDs/PCFDs in stationary source emissions. Results are provided here for a total of twenty-three (23) samples (reported as pairs) representing twelve (12) 30 d sampling events conducted at a site located in metropolitan Hartford CT. Samples were collected in winter months during calendar years 2002-2008. PCDDs/PCDFs concentration data (pg m−3) are reported as both congener sums (Cl4-Cl8) and 2378-substitued congeners. Total PCDDs/PCDFs concentrations for these twelve (12) sampling events ranged from 0.68 pg m−3 (2003) to 4.18 pg m−3 (2004) with a mean concentration of 2.04 pg m−3.Method performance was monitored through use of collocated samples, in field isotopically labeled compounds, isotopically labeled laboratory applied internal standards and field blank samples. Method performance consistently exceeded goals established in USEPA Method TO9A for these same parameters. Average recoveries of in field labeled PCDDs/PCDFs ranged from 97.5% to 104.2%. Average (mean) recoveries for each of the ten (10) isotopically labeled internal standards ranged from 77.0% (13C-OCDF) to 95.5% (13C-2,3,7,8-TCDF). Method precision defined as % RPD data for collocated sampler pairs ranged from 8% to 14% for PCDDs and from 5% to 12% for PCDFs. The mean RPD for all PCDDs/PCDFs combined is 9.6%. Field monitoring results demonstrate method sensitivity for all PCDDs/PCDFs congeners and 2378-substituted congeners to be well below concentrations typically found for these compounds in ambient air (all reported data represent measured concentrations). Quantities (pg) found in field blanks represent the major determinant to achieving further enhancements in method sensitivity for selected congeners (OCDD < 42 fg m−3; 1,2,3,4,6,7,8-HpCDD < 5.7 fg m−3; and 1,2,3,4,6,7,8-HpCDF < 2.1 fg m−3). The CTDEP method represents a highly sensitive and reliable technique for monitoring of PCDDs/PCDFs congeners and other persistent organic pollutants (POPs) at ultra trace levels in ambient air (fg m−3). 相似文献
66.
Barend L. van Drooge 《Environmental pollution (Barking, Essex : 1987)》2010,158(9):2880-2887
The ambient air in Northern Italy is characterised by relatively high PAH and PM10 concentrations in relation to calm wind and intensive temperature inversions, especially during cold periods. These stagnant conditions are occasionally interrupted by North-Föhn events, which cause a drop in relative humidity and an increase in O3 levels, indicating the mixing of local and free troposphere air flows. In this study the influence of the North-Föhn on concentrations of tracer organic compounds, including polycyclic aromatic hydrocarbons (PAHs), PM10, O3 and black carbon (BC) was studied during a North-Föhn event in November 2007. Large fluctuations in the concentration of these compounds, as well as changes in PM10 composition due to daytime and night-time variations of local source emissions were observed. Although these events occur at low frequencies (6-10%) they can for short periods, strongly affect the regional air quality by quickly decreasing the concentrations of these tracer organic compounds. 相似文献
67.
对现场监测环境空气中PM10 的两种测定方法—β射线衰减法和微量振荡天平法的测量作了对比实验。实验表明 ,两种测定方法的结果具有一致性、相关性和可比性 ,能用回归直线方程来描述两者之间的关系。β射线衰减法的测定结果平均高于微量振荡天平法 15 8% ,它们之间平均偏差为 7 5 %。微量振荡天平法在现场测定中受干扰物和不确定因素的影响较少 ,其测量准确性优于 β射线衰减法。两种监测仪的运行费用大致相同 ,维护量和故障率均 较低 相似文献
68.
在烟草加工的加香工序,挥发的酒精和搅拌混料产生的烟草粉尘形成气粉混合体系,其燃爆特性相较于单相烟草粉尘有较大变化。对20 L爆炸球进行了部分改造,可完成20℃~80℃环境温度、100%LEL以下酒精蒸气浓度、最大2 J电火花能量组合的气粉混合物的最小点火能测试。选用烘丝和加香烟草粉尘做对比,探究了环境温度和酒精蒸气浓度对酒精蒸气/烟草粉尘两相混合体系点火能的影响规律。结果表明:相同环境温度下,加香烟草粉尘的最小点火能比烘丝烟草粉尘低;加香粉尘、烘丝粉尘及混合体系的最小点火能随环境温度变化的趋势一致,均随温度的升高而降低;加入10%LEL的酒精蒸气后,相同温度下气粉混合体系的最小点火能低于单相烟草粉尘。随着环境温度的升高,二者的差值逐渐减小,酒精蒸气诱导烟草粉尘最小点火能降低的能力逐步减小甚至消失;在电点火条件下,当酒精蒸气浓度低于50%LEL时,气粉混合体系较难被点燃,当酒精蒸气浓度高于75%LEL时,混合体系较易被点燃。 相似文献
69.
采用~(32)P后标记分析法,测定上海市大气飘尘中致癌物与DNA形成加合物的能力。先将飘尘行机提取物,按一定剂量涂抹到小鼠皮肤上作用一定时间;然后,处死小鼠,取涂抹部位皮肤提取DNA,用~(32)P后标记法分离测定DNA中致癌物,即DNA加合物。结果表明,上海市大气飘尘有机提取物可以与皮肤DNA形成多个加合物斑点,提示上海市大气飘尘存在一定的致癌危险性。 相似文献
70.
François Zimmermann Marie-Thérèse Lecler Frédéric Clerc Alain Chollot Eric Silvente Jérome Grosjean 《Waste management (New York, N.Y.)》2014,34(7):1257-1263
The fluorescent lamp recycling sector is growing considerably in Europe due to increasingly strict regulations aimed at inciting the consumption of low energy light bulbs and their end-of-life management. Chemical risks were assessed in fluorescent lamp recycling facilities by field measurement surveys in France, highlighting that occupational exposure and pollutant levels in the working environment were correlated with the main recycling steps and processes.The mean levels of worker exposure are 4.4 mg/m3, 15.4 μg/m3, 14.0 μg/m3, 247.6 μg/m3, respectively, for total inhalable dust, mercury, lead and yttrium. The mean levels of airborne pollutants are 3.1 mg/m3, 9.0 μg/m3, 9.0 μg/m3, 219.2 μg/m3, respectively, for total inhalable dust, mercury, lead and yttrium. The ranges are very wide. Surface samples from employees’ skin and granulometric analysis were also carried out. The overview shows that all the stages and processes involved in lamp recycling are concerned by the risk of hazardous substances penetrating into the bodies of employees, although exposure of the latter varies depending on the processes and tasks they perform. The conclusion of this study strongly recommends the development of a new generation of processes in parallel with more information sharing and regulatory measures. 相似文献