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191.
Bio-F生物吸附剂对水中铁锰的去除与特性   总被引:1,自引:0,他引:1  
以Bio-F(Bio-F生物吸附剂)为材料,研究其对水中Fe2+和Mn2+的去除能力与特性. 结果表明,Bio-F可同时去除水中Fe2+和Mn2+且吸附过程符合Lagergren一级动力学模型. Langmuir吸附等温线能较好地描述Bio-F吸附Fe2+和Mn2+的过程,表现为单分子层化学优惠吸附,其对Fe2+和Mn2+的最大饱和吸附量分别达491和380 mgg. Bio-F对Fe2+和Mn2+的吸附为吸热反应且在pH 6~7范围内可保持86%以上吸附能力(P>005). 较高的c(Ca2+)和c(Mg2+)可明显抑制Bio-F去除Fe2+和Mn2+的能力(P<005),但高c(PO43-)则可促进该吸附过程(P>005). Bio-F经10次再生后对Fe2+和Mn2+的去除率分别达9727%和9467%. Bio-F无毒安全,采用Bio-F处理高铁锰饮用水具有应用潜力.   相似文献   
192.
A series of hierarchical macro-/mesoporous silica supports (MMSs) were successfully synthesized using dual-templating technique employing polystyrene (PS) spheres and the Pluronic P123 surfactant. Pd was next loaded on the hierarchical silica supports via colloids precipitation method. Physicochemical properties of the synthesized samples were characterized by various techniques and all catalysts were tested for the total oxidation of o-xylene. Among them, the Pd/MMS-b catalyst with tetraethoxysilane/polystyrene weight ratio of 1.0 exhibited superior catalytic activity, and under a higher gas hourly space velocity (GHSV) of 70000 h–1, the 90% conversion of o-xylene has been obtained at around 200°C. The BET and SEM results indicated that Pd/MMSb catalyst possesses high surface area and large pore volume, and well-ordered, interconnected macropores and 2D hexagonally mesopores hybrid network. This novel ordered hierarchical porous structure was highly beneficial to the dispersion of active sites Pd nanoparticles with less aggregation, and facilitates diffusion of reactants and products. Furthermore, the Pd/MMS-b catalyst possessed good stability and durability.  相似文献   
193.
Both raw water and chlorinated drinking water samples were collected from and the Liu‐Du water treatment plant in northern Taiwan from October 1990 to April 1992. The polycyclic aromatic hydrocarbons (PAHs) and mutagenicity in these water samples were analyzed by GC/MS and Ames test. The Mutagenicity/DMSO (Dimethyl Sulfoxide) ratio in S. typhimurium TA98 and TA100 with or without S9 mixture increased, even higher than 2, following the sequence of unit process. It was observed that the mutagenicity with TA98 (S9+) was highly related to most of PAHs in the raw water; while the mutagenicity with TA98 (S9+) was only correlated with DbA and BghiPr in the treated water. It could be expected that the mutagenicity level was controlled by other predominant components after the raw water was treated, for example, the chlorination process.  相似文献   
194.
The objectives of this research were to identify the surface chemical features of activated carbons made of peat, bituminous coal and coconut shell, as well as examine the specific relationship of these properties by using statistical analyses. The results showed that the peat carbons contained much more amounts of Ca, S, P and Mg; however, the bituminous carbons possessed higher contents of Si, Al and Fe. In addition, the content ratios of Al to Si exhibited the Al enrichment phenomenon occurred after the heat treatment. A nonlinear correlation between the pH value and the difference in the amounts of basic and acidic groups was developed. Unfortunately, there were no specific mass ratios found among the acidic functional groups. The results of correspondence analysis (CA) gave a promising confirmation about the EDXRF analysis; moreover, the results of factor analysis (FA) fairly agreed with the findings suggested by CA. Both could explain the specific chemical features of activated carbons made from different materials, especially the CA could differentiate each other in detail.  相似文献   
195.
不同土地利用方式对赤红壤理化性质的综合影响   总被引:2,自引:0,他引:2  
通过比较不同土地利用方式下赤红壤pH值、粘粒、容重、孔隙度、有机碳、氮磷钾全量及其速效养分含量的差异,并运用主成分分析方法分析各变量的相互关系、土壤综合理化特征及其关键改良因子。研究结果表明:新垦旱地容重最高,粘粒含量和孔隙度最低;有机碳、全量氮磷钾养分和速效氮磷养分含量均处于较低水平(P<0.05)。果园土容重显著低于其他土地利用方式土壤,且全氮、碱解氮和速效磷钾水平均处于较高水平(P<0.05)。桉树林的全钾和速效钾含量显著高于灌木林,而粘粒含量和速效磷含量相对较低(P<0.05)。主成分分析结果显示:新垦旱地、果园和桉树林、灌木林土壤理化综合质量差异显著(P<0.05),其中新垦旱地当前质量相对较差。有机碳、全氮和速效氮养分缺乏是当前新垦旱地土壤理化质量较差的主要原因。较少的速效磷钾养分含量是当前桉树林地、灌木林土壤质量的限制因素。主成分分析不仅能够区分不同土地利用方式下赤红壤理化质量差异,而且也是探查改良土壤质量因子的有效方法。  相似文献   
196.
A number of important rivers of Romania were investigated for pharmaceutical and antifungal residues. In a post target approach analysis, a single-stage, high-resolution mass spectrometry was successfully applied for the screening of 43 pharmaceuticals and fungicides in water, using U-HPLC-Exactive Orbitrap MS at 50,000 full width at half maximum resolution. Detection was based on accurate masses and retention times. The study confirmed the presence of pharmaceuticals and antifungals such as diclofenac, sulfamethoxazole, carbamazepine, trimethoprim, thiabendazole, and clotrimazole, in water. Diclofenac and carbamazepine were the most frequently detected (eight samples); concentrations ranged from 5 to 50 ng L?1. Low concentrations of griseofulvin were detected in the Prut River. Further monitoring studies should be carried out in order to fill the gaps of knowledge concerning the presence of pharmaceutical residues in Romanian water environment and to improve public understanding regarding the environmental risk of pharmaceutical contamination.  相似文献   
197.
螳螂是田间控制害虫种群增加的重要捕食性天敌之一。以中华大刀螂3龄幼虫(Paratenodera sinensis Saussure)为受试生物,利用9种常用杀虫剂配制成不同浓度梯度的药剂,通过喷雾法直接暴露,分别测定了LC50和死亡率来评价不同杀虫剂对中华大刀螂毒性和危害程度的影响。结果显示,9种杀虫剂对中华大刀螂幼虫的毒性(LC50值)差异很大,用药后24h的LC50在0.7182~347.7962mg·L-1之间,LC95在8.8057~1734.5650mg·L-1之间;用药后48h的LC50在0.3564~193.6887mg·L-1之间,LC95在3.8958~1548.3258mg·L-1之间;用药后72h的LC50在0.2232~115.3391mg·L-1之间,LC95在1.7730~530.6462mg·L-1之间。不同杀虫剂对中华大刀螂幼虫的毒性差异最高达到543.46倍。毒性大小依次为,高效氯氟氰菊酯﹥啶虫脒﹥联苯菊酯﹥毒死蜱﹥噻虫嗪﹥茚虫威﹥吡虫啉﹥阿维菌素﹥苏云金杆菌原粉(Bt)。根据田间推荐浓度处理的死亡率判断,毒死蜱、联苯菊酯、啶虫脒、高效氯氟氰菊酯为有害水平,Bt为中度有害水平,吡虫啉、茚虫威、噻虫嗪为微害水平,阿维菌素接近无害水平。根据LC50与田间推荐浓度的比值判断,阿维菌素、吡虫啉对螳螂种群数量不会产生太大影响;Bt、茚虫威和噻虫嗪对螳螂种群数量会产生一定危害;而毒死蜱、啶虫脒、联苯菊酯和高效氯氟氰菊酯将严重影响螳螂种群数量的稳定性。在24~72h范围内,不同杀虫剂LC50和LC95随施药时间的延长而降低,说明暴露时间越长毒性越大,危害程度也越大。建议在中华大刀螂生活范围内减少高效氯氟氰菊酯、联苯菊酯、啶虫脒和毒死蜱的施用,推荐杀虫剂田间使用量时,除考虑对防治对象的防效,还应考虑对天敌种群的危害,提高药剂使用安全性,保护天敌种群的稳定性。  相似文献   
198.
The amount of atmospheric nitrogen (N) deposited on the land surface has increased globally and by nearly five times in China from 1901 to 2005. Little is known about how elevated reactive N input has affected the carbon (C) sequestration capability of China's terrestrial ecosystems, largely due to the lack of reliable data on N deposition. Here we have used a newly developed data set of historical N deposition at a spatial resolution of 10 km x 10 km in combination with other gridded historical information on climate, atmospheric composition, land use, and land management practices to drive a process-based ecosystem model, the dynamic land ecosystem model (DLEM) for examining how increasing N deposition and its interactions with other environmental changes have affected C fluxes and storage in China's terrestrial ecosystems during 1901-2005. Our model simulations indicate that increased N deposition has resulted in a net C sink of 62 Tg C/yr (1 Tg = 1012 g) in China's terrestrial ecosystems, totaling up to 6.51 Pg C (1 Pg = 10(15) g) in the past 105 years. During the study period, the N-induced C sequestration can compensate for more than 25% of fossil-fuel CO2 emission from China. The largest C sink was found in southeast China, a region that experienced the most significant increase of N deposition in the period 1901-2005. However, the net primary productivity induced by per-unit N deposition (referred to as ecosystem N use efficiency, ENUE, in this paper) has leveled off or declined since the 1980s. This indicates that part of the deposited N may not be invested to stimulate plant growth, but instead leave the ecosystem by various pathways. Except shrubland and northwest/southwest China, signs of N saturation are apparent in the rest major biome types and regions, with ENUE peaking in the 1980s and leveling off or declining thereafter. Therefore, to minimize the excessive N pollution while keeping the N-stimulated C uptake in China's terrestrial ecosystems, optimized management practices should be taken to increase N use efficiency rather than to keep raising N input level in the near future.  相似文献   
199.
Thermal degradation of triacetone triperoxide (TATP) was studied using differential scanning calorimetry (DSC) and gas chromatography/mass spectrometry (GC/MS). TATP, a potential explosive material, is powerful organic peroxide (OP) that can be synthesized by available chemicals, such as acetone and hydrogen peroxide in the laboratory or industries. The thermokinetic parameters, such as exothermic onset temperature (T0) and heat of decomposition (ΔHd), were determined by DSC tests. The gas products from thermal degradation of TATP were identified using GC/MS technique.In this study, H2O2 was mixed with propanone (acetone) and H2SO4 catalysis that produced TATP. The T0 of TATP was determined to be 40 °C and Ea was calculated to be 65 kJ/mol. A thermal decomposition peak of H2O2 was analyzed by DSC and two thermal decomposition peaks of H2O2/propanone were determined. Therefore, H2O2/propanone mixture was applied to mix acid that was discovered a thermal decomposition peak (as TATP) in this study. According to risk assessment and analysis methodologies, risk assessment of TATP for the environmental and human safety issue was evaluated as 2-level of hazard probability rating (P) and 6-level of severity of consequences ratings (S). Therefore, the result of risk assessment is 12-point and was evaluated as “Undesirable” that should be enforced the effect of control method to reduce the risk.  相似文献   
200.
针对目前多种光纤感测技术应用于管道渗漏监测中的不足,利用蒸发式湿度测量原理,提出了一种基于FBG技术的管道渗漏监测方法,并设计了试验对其可行性及影响因素进行探究。结果表明:该方法在湿度约为80%RH的环境中能测出1.84℃的渗漏稳定温差,具有良好的可行性;此外,风速、水温两个因素会对稳定温差产生影响,渗漏量这一因素不影响稳定温差,仅影响温差响应的等待时长,该方法在风速较大、水温较低的环境因素下具有更加良好的渗漏监测效果。  相似文献   
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