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81.
The identities and concentrations of low-molecular-weight organic acids (LMWOAs) were determined by ion chromatography throughout a 20-m water column in Hongfeng Lake, China. The spatiotemporal variations of LMWOAs and their contributions to dissolved organic matter (DOM) in a research period of 24 hr were also investigated. The results demonstrated that five LMWOAs (lactic, acetic, pyruvic, sorbic, oxalic acid) were detected, and their total concentration and proportion in DOC were 6.55 μmol/L and 7.47%. Their average levels were 2.50, 0.65, 2.35, 0.96 and 0.09 μmol/L, respectively. LMWOAs were higher during daytime (10:00-18:00 on Jun 13, 2008) than nighttime (21:00-6:00 the next morning), in particular 4.99 μmol/L high in the epilimnion ( 1 m water depth), reflecting the fact that direct import from terrigenous sources and photochemical production from humic materials were dominant during LMWOAs’ origin and accumulation. The same factors caused LMWOAs to be 0.63 μmol/L in the epilimnion higher than in the hypolimnion. The rapid decrease of total organic acid (TOA) up until 18:00 mainly resulted from bio-uptake and mineralization in the hypolimnion (>1 m water depth). Pyruvic acid increased with time in the epilimnion and decreased in the hypolimnion, largely related to the two contrary processes of continuous degradation and synthesis of macromolecular organic matter during life materials’ cycle mediated by organisms. Simultaneously, plankton behavior and thermal stratification played a pivotal role in LMWOAs’ behavior in the water column, causing decreasing and increasing profiles. The distribution of LMWOAs represents an interesting resource for biogeochemical research of DOM in aquatic ecosystems.  相似文献   
82.
We have studied the integrated model of reaction rate equations with thermal energy balance in aerobic bioreactor for food waste decomposition and showed that the integrated model has the capability both of monitoring microbial activity in real time and of analyzing biodegradation kinetics and thermal-hydrodynamic properties. On the other hand, concerning microbial metabolism, it was known that balancing catabolic reactions with anabolic reactions in terms of energy and electron flow provides stoichiometric metabolic reactions and enables the estimation of microbial biomass yield (stoichiometric reaction model). We have studied a method for estimating real-time microbial biomass yield in the bioreactor during food waste decomposition by combining the integrated model with the stoichiometric reaction model. As a result, it was found that the time course of microbial biomass yield in the bioreactor during decomposition can be evaluated using the operational data of the bioreactor (weight of input food waste and bed temperature) by the combined model. The combined model can be applied to manage a food waste decomposition not only for controlling system operation to keep microbial activity stable, but also for producing value–added products such as compost on optimum condition.  相似文献   
83.
The reactions of gas-phase anthracene and suspended anthracene particles with O3 and O3-NO were conducted in a 200-L reaction chamber, respectively. The secondary organic aerosol (SOA) formations from gas-phase reactions of anthracene with O3 and O3-NO were observed. Meanwhile, the size distributions and mass concentrations of SOA were monitored with a scanning mobility particle sizer (SMPS) during the formation processes. The rapid exponential growths of SOA reveal that the atmospheric lifetimes of gas-phase anthracene towards O3 and O3-NO are less than 20.5 and 4.34 hr, respectively. The particulate oxidation products from homogeneous and heterogeneous reactions were analyzed with a vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer (VUV-ATOFMS). Gas chromatograph/mass spectrometer (GC/MS) analyses of oxidation products of anthracene were carried out for assigning the time-of-flight (TOF) mass spectra of products from homogeneous and heterogeneous reactions. Anthrone, anthraquinone, 9,10- dihydroxyanthracene, and 1,9,10-trihydroxyanthracene were the ozonation products of anthracene, while anthrone, anthraquinone, 9-nitroanthracene, and 1,8-dihydroxyanthraquinone were the main products of anthracene with O3-NO.  相似文献   
84.
Many studies have shown soil degradation after the conversion of native forests to exotic Eucalyptus plantations. However, few studies have investigated the long-term impacts of short-rotation forestry practices on soil microorganisms. The impacts of Eucalyptus successive rotations on soil microbial communities were evaluated by comparing phospholipid fatty acid (PLFA) abundances, compositions, and enzyme activities of native Pinus massoniana plantations and adjacent 1st, 2nd, 3rd, 4th generation Eucalyptus plantations. The conversion from P. massoniana to Eucalyptus plantations significantly decreased soil microbial community size and enzyme activities, and increased microbial physiological stress. However, the PLFA abundances formed "U" shaped quadratic functions with Eucalyptus plantation age. Alternatively, physiological stress biomarkers, the ratios of monounsaturated to saturated fatty acid and Gram+ to Gram- bacteria, formed "∩" shaped quadratic functions, and the ratio of cy17:0 to 16: 1ω7c decreased with plantation age. The activities of phenol oxidase, peroxidase, and acid phosphatase increased with Eucalyptus plantation age, while the cellobiobydrolase activity formed "U" shaped quadratic functions. Soil N:P, alkaline hydrolytic nitrogen, soil organic carbon, and understory cover largely explained the variation in PLFA profiles while soil N:P, alkaline hydrolytic nitrogen, and understory cover explained most of the variability in enzyme activity. In conclusion, soil microbial structure and function under Eucalyptus plantations were strongly impacted by plantation age. Most of the changes could be explained by altered soil resource availability and understory cover associated with successive planting of Eucalyptus. Our results highlight the importance of plantation age for assessing the impacts of plantation conversion as well as the importance of reducing disturbance for plantation management.  相似文献   
85.
以磁性材料为原料,经过特定的工艺处理,对多孔陶瓷进行磁化改性获得磁性多孔载体,并将该载体应用于生物膜反应器中进行焦化废水处理试验。对不同类型的多孔陶粒载体进行对比试验,结果表明:磁性载体生物膜反应器对COD、NH3-N的去除率比普通活性污泥法高出25%30%,比非载体生物膜反应器高出15%30%,比非载体生物膜反应器高出15%20%左右。反应器的曝气量为1.5 L/h,曝气时间为10 h/d,温度为2520%左右。反应器的曝气量为1.5 L/h,曝气时间为10 h/d,温度为2530℃。焦化废水经磁性载体生物膜反应器处理后,上清液中COD,NH3-N的去除率均在90%左右。出水浓度达到国家工业废水排放二级标准(GB18918-2002)。  相似文献   
86.
潜流人工湿地处理农村生活污水动力学研究   总被引:2,自引:0,他引:2  
考察潜流人工湿地处理农村生活污水的运行效果,并探寻一级动力学常数的空间变化情况,采用"厌氧调节池+二级串联潜流式人工湿地"工艺处理农村生活污水。结果表明,经过3个月运行后人工湿地对污水中COD、TP、TN和NH3-N的去除率分别达到了79.13%,71.54%,57.26%和60.01%。通过湿地原位检测显示以上各类污染物在生物床内都有较明显的沿程下降趋势,在床体的前半部分污染物的降解较快,后半部分相对缓慢。农村生活污水中污染物去除动力学符合一级动力学模型,一级生物床中COD、TP、TN和NH3-N的去除,Kv均值分别为3.048、2.469、1.625和1.695;二级生物床中Kv均值分别为2.542、1.946、1.383和1.453。生物床Kv呈现出减小的趋势说明生物床前端对各类污染物的降解速率比后端快。生物床间的跌水池的复氧,增加了二级生物床前端的Kv,提高了对污染物的降解速率。  相似文献   
87.
以炼钢过程中排放的固体废弃物钢渣为碳捕获剂,进行了钢渣湿法捕获烟气CO2工艺的实验研究。通过分析钢渣的组成成份及反应机理,研究液固比、反应温度、反应时间、pH值及反应产物等主要参数对钢渣湿法碳捕获状况的影响。实验证明,通过合理的设计和适当的操作,可使钢渣湿法碳捕获效率达60%以上,具有一定的应用价值。  相似文献   
88.
丛枝菌对转Bt基因棉根际土壤营养物质及酶活性的影响   总被引:1,自引:0,他引:1  
尹念辅  杨兵  李铁松  戈峰 《环保科技》2013,(5):35-39,42
转Bt基因抗虫棉已在全球范围内广泛种植,然而Bt棉根际分泌物是否会影响土壤理化性质及土壤功能尚缺乏深入研究。通过盆栽实验方法,设计不同的棉花品种与是否接种丛枝菌总共4个处理,以此研究Bt棉和接种丛枝菌根真菌对植物根际土壤营养物质含量以及土壤酶活性的影响。结果显示:丛枝菌可以使non-Bt棉和Bt棉根际土壤营养物质中的土壤有机质和土壤总氮含量显著增加,但是对根际土壤全磷却鲜有影响。转基因对于不同品种棉花根际土壤酶,丛枝菌均能有效增强其活性。由此表明,丛枝菌对Bt棉和non-Br棉根际土壤环境均具有改善作用。  相似文献   
89.
水体系中氧氟沙星的光化学降解研究   总被引:3,自引:3,他引:0  
邵萌  杨桂朋  张洪海 《环境科学》2012,33(2):476-480
研究了高压汞灯和氙灯照射下氧氟沙星(OFLX)在蒸馏水、人工海水和天然海水中的光降解过程,探讨了光源、起始浓度、丙酮、表面活性剂等因素对OFLX光化学降解速率的影响.结果表明,OFLX在高压汞灯下的光反应速率比在氙灯下快得多,均符合一级反应动力学过程;在相同光源下,OFLX在海水中降解最快,其次是人工海水;当OFLX初始浓度为2、4、6mg.L-1时,其光解速率常数分别为0.163、0.140和0.132 min-1,随着OFLX初始浓度增大,其光解率降低;不同浓度的丙酮均能促进OFLX光降解的反应,其反应速率常数为0.084 2~0.102 min-1,且光敏效率与丙酮浓度呈正相关关系;然而当十六烷基三甲基溴化铵(CTAB)、十二烷基苯磺酸钠(SDBS)、吐温-20(TW-20)等表面活性剂的浓度为5 mg.L-1,它们均抑制了水体中OFLX光降解反应的进程.另外,利用金藻8701单种培养进行了OFLX光化学降解前后的毒性试验,表明OFLX光解过程产生风险较高的中间产物,随着光解进行,产物毒性降低.  相似文献   
90.
化石燃料原油和原煤的燃烧、含钒矿石的开采和冶炼是大气中重金属钒的主要来源。文章利用重金属钒的排放系数分析了中国1978-2010年人为过程释放到大气中重金属钒的总量和行业重金属钒的排放,预测了2020年和2030年中国大气中重金属钒的排放量。结果表明,自1978年以来,中国钒的排放量增加了4倍,中国2010年人类活动向大气排放的重金属钒总量达3.18万吨,约占世界总量的12%。原油燃烧释放到大气中的钒约占总量的85%,煤炭燃烧的排放量占10.5%,其中工业耗油向大气中释放重金属钒的比例从1980的71%下降到2008年的42%,总量从3 721 t增加至9 361 t;交通运输行业从10%上升到36%,总量从547 t增加至7 967 t;其它行业(农林牧渔水利业、批发零售业和住宿餐饮业、生活消费)基本维持在20%左右,总量从986 t增加至5 052 t。因此,应加强大气中钒的监测和管理,预防大气钒污染事件的发生。  相似文献   
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