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991.
Derivation of predicted no effect concentrations (PNEC) for 2,4,6-trichlorophenol based on Chinese resident species 总被引:4,自引:0,他引:4
2,4,6-Trichlorophenol (2,4,6-TCP) is a common chemical intermediate and a by-product of water chlorination and combustion processes, and is a priority pollutant of the aquatic environment in many countries. Although information on the toxicity of 2,4,6-TCP is available, there is a lack of information on the predicted no-effect concentration (PNEC) of 2,4,6-TCP, mainly due to the shortage of chronic and site-specific toxicity data. In the present study, acute and sub-chronic toxicity of 2,4,6-TCP on six different resident Chinese aquatic species were determined. PNEC values were calculated and compared by use of two approaches: assessment factor (AF) and species sensitivity distribution (SSD). Values for acute toxicity ranged from 1.1 mg L−1 (Plagiognathops microlepis) to 42 mg L−1 (Corbicula fluminea) and the sub-chronic no observed effect concentrations (NOECs) ranged from 0.05 mg L−1 (Mylopharyngodon piceus) to 2.0 mg L−1 (C. fluminea). PNECs obtained by the assessment factor approach with acute (AF = 1000, 0.001 mg L−1) or chronic (AF = 10, 0.005 mg L−1) toxicity data were one order of magnitude less than those from SSD methods (0.057 mg L−1). PNEC values calculated using SSD methods with a 50% certainty for 2,4,6-TCP was less than those obtained by use of the USEPA recommend final chronic value (FCV) method (0.097 mg L−1) and the one obtained by use of the USEPA recommend acute-to-chronic (ACR) methods (0.073 mg L−1). PNECs derived using AF methods were more protective and conservative than that derived using SSD methods. 相似文献
992.
The dissolution of the 2,4,6-trinitrotoluene (TNT), hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) from microscale particles (<250 μm) of the explosive formulation Composition B was examined and compared to dissolution from macroscopic particles (>0.5 mm). The dissolution of explosives from detonation soot was also examined. The measured mass transfer coefficients for the microscale particles were one to two orders of magnitude greater than the macroscopic particles. When normalized to particle surface area, mass transfer coefficients of microscale and macroscale particles were similar, indicating that the bulk dissolution processes were similar throughout the examined size range. However, an inverse relationship was observed between the particle diameter and the RDX:TNT mass transfer rate coefficient ratio for dry-attritted particles, which suggests that RDX may be more readily dissolved (relative to TNT) in microscale particles compared to macroscale particles. Aqueous weathering of larger Composition B residues generated particles that possessed mass transfer coefficients that were on the order of 5- to 20-fold higher than dry-attritted particles of all sizes, even when normalized to particle surface area. These aqueous weathered particles also possessed a fourfold lower absolute zeta-potential than dry-attritted particles, which is indicative that they were less hydrophobic (and hence, more wettable) than dry-attritted particles. The increased wettability of these particles provides a plausible explanation for the observed enhanced dissolution. The wetting history and the processes by which particles are produced (e.g., dry physical attrition vs. aqueous weathering) of Composition B residues should be considered when calculating mass transfer rates for fate and transport modeling. 相似文献
993.
2种人工湿地的水力停留时间及净化效果 总被引:2,自引:0,他引:2
以复合垂直流人工湿地(IVCW)和水平潜流人工湿地(HSCW)为研究对象,研究了2种湿地运行的季节性最佳水力停留时间(HRT)参数,并监测了2种湿地在最佳HRT参数下运行时对污水的净化效果。结果显示:(1)在IVCW中,最佳HRT在春、秋季为8~10 h;夏季为6 h;冬季为12 h。在HSCW中,最佳HRT在春、秋季为10~12 h;夏季为6~8h;冬季为24~36 h。(2)2种湿地对COD的去除率均无显著的季节性差异;湿地进水中NH4+-N/TN比值与TN去除率显著负相关;不同季节下IVCW对TN的去除效果均高于HSCW。(3)水温对TN、TP去除率的影响在IVCW中比HSCW中的明显;水温高时,2种湿地中的TN去除率较高,IVCW中的TP去除率也较高,但HSCW中的TP去除率则较低,它们间均未达到显著的相关性。 相似文献
994.
995.
996.
997.
Jin Ma Li-bo Pan Qin Wang Chun-ye Lin Xiao-li Duan Hong Hou 《Environmental geochemistry and health》2018,40(1):295-301
A total of 60 children (31 males and 29 females) between the ages of 3 and 12 years were randomly selected from Lanzhou City in Gansu Province, northwest China. Hand (soil/dust) SD samples from these children were collected using hand wipes. We determined the approximate amounts of hand SD and the concentrations of three tracer soil elements (Ce, Y, and V) in these samples. The approximate amounts of hand SD ranged from 42.28 to 173.76 mg, with a median value of 85.42 mg. In addition, the mean amounts of hand SD estimated using the concentrations of Ce, Y, and V in the samples were 4.63, 3.43, and 3.42 mg, respectively. The amount of hand SD varied greatly among the age groups: primary school children had more hand SD than kindergarten children, males had more hand SD than females, and children from rural areas had more hand SD than those from urban areas. The rates of daily ingestion of hand SD for kindergarten and primary school children were estimated to be 7.73 and 6.61 mg/day, respectively. 相似文献
998.
通过FT-IR和GC—MS检测分析,表明了压裂废水中有机物主要以苯环结构为主的芳香类化合物和其他杂环化合物,苯环及杂环上的主要官能团包括酮、酯、羧酸、醛、酚、氨基等。同时,压裂废水中的粘度为常规水粘度的2~3倍。针对压裂废水高粘度和高COD污染水质特征,实验研究了压裂废水二氧化锰臭氧催化氧化处理特性以及粘度对处理效果的影响,研究结果表明,在粘度较高(2.2×10-3 Pa·s)压裂废水中,投加的化学药剂很难扩散,羟基自由基·OH的利用效率较低,处理效果较差。通过投加过硫酸钾(5g/L)降粘后,可在很大程度上提高二氧化锰臭氧催化氧化的处理效果。通过对压裂废水中有机物分子量分布、FT-IR分析以及GC—MS分析可知,二氧化锰臭氧催化氧化处理压裂废水是通过激发羟基自由基,破坏水中有机物极性和有机物化学构造,将复杂长链有机物转变为简单有机物,其出水COD可达到国家污水综合排放标准中的二级排放标准。 相似文献
999.
Yunhai Wu Yajun Wen Jianxin Zhou Julin Cao Yanping Jin Yunying Wu 《Environmental science and pollution research international》2013,20(4):2210-2219
This study evaluates the behavior of coconut charcoal (AC) to adsorb Cr(VI), As(III), and Ni(II) in mono- and multicomponent (binary and ternary) systems. Batch experiments were carried out for mono- and multicomponent systems with varying metal ion concentrations to investigate the competitive adsorption characteristics. The adsorption kinetics followed the mechanism of the pseudo-second-order equation in both single and binary systems, indicating chemical sorption as the rate-limiting step of adsorption mechanism. Equilibrium studies showed that the adsorption of Cr(VI), As(III), and Ni(II) followed the Langmuir model and maximum adsorption capacities were found to be 5.257, 0.042, and 1.748 mg/g, respectively. In multicomponent system, As(III) and Ni(II) adsorption competed intensely, while Cr(VI) adsorption was much less affected by competition than As(III) and Ni(II). With the presence of Cr(VI), the adsorption capacities of As(III) and Ni(II) on AC were higher than those in single system and the metal sorption followed the order of Ni(II)?>?As(III)?>?Cr(VI). The results from the sequential adsorption–desorption cycles showed that AC adsorbent held good desorption and reusability. 相似文献
1000.
A new class of nano-scale Fe0 particles (NZVI) supported on a PAA/PVDF membrane (NZVI-PAA/PVDF) were synthesized and the feasibility of using NZVI-PAA/PVDF for reductive immobilization of Cr(VI) in water was investigated through laboratory batch tests. The results showed that the Cr(VI) removal capacity of NZVI-PAA/PVDF was 181 mg Cr/g Fe at an initial Cr(VI) concentration of 20 mg L(-1) under pH 6.5 +/- 0.1. XPS results showed that Cr(VI) was converted to nontoxic Cr(III). Interfering ions exerted various degrees of impact on NZVI-PAA/PVDF's Cr(VI) removal capacity. Specifically, Ca2+ alone showed the mildest impact while the presence of ions (Mg2+ and HCO3-) exerted the greatest impact. An advantage of NZVI-PAA/PVDF is that the nano-scale Fe0 and resultant particles were combined within a PAA/PVDF membrane, which prevents secondary pollution. Moreover, a piece of PAA/PVDF membrane (4.7 cm diameter) can still support 6.51 mg of nano-scale Fe0 particles after being renewed. 相似文献