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41.
Steel manufacturing byproducts and commercial iron powders were tested in the treatment of Ni^2+-contaminated water. Ni^2+ is a priority pollutant of some soils and groundwater. The use of zero-valent iron, which can reduce Ni^2+ to its neural form appears to be an alternative approach for the remediation of Ni^2+-contaminated sites. Our experimental data show that the removal efficiencies of Ni^2+ were 95.15% and 94.68% at a metal to solution ratio of 20 g/L for commercial iron powders and the steel manufacturing byproducts in 60 min at room temperature, respectively. The removal efficiency reached 98.20% when the metal to solution ratio was 40 g/L for commercial iron powders. Furthermore, we found that the removal efficiency was also largely affected by other factors such as the pHs of the treated water, the length of time for the metal to be in contact with the Ni^2+-contaminated water, initial concentrations of metal solutions, particle sizes and the amount of iron powders. Surprisingly, the reaction temperature appeared to have little effect on the removal efficiency. Our study opens the way to further optimize the reaction conditions of in situ remediation of Ni^2+ or other heavy metals on contaminated sites.  相似文献   
42.
本文采用HNO_3、HCl-HNO_3、HNO_3-H_2SO_4-HClO_4,溶洋方法消解土样,用原子吸收法测定题述中的元素,并与HCl-HNO_3-HF-HClO_4全消解方法进行了比较.发现除用HF以外的其它酸溶法Pb、Cr的溶出较少溶出比分别低于55%和67%,主要原因是Pb、Cr包藏在土壤的矿物晶格中。  相似文献   
43.
Cyprinus carpio were exposed to two non-essential (Hg and Pb)and two essential (Cu and Ni) heavy metal salts at lethal andsub-lethal concentrations. Blood serum total protein, serum globulinand serum albumin was analysed every 2 hr for 24 hrs andagain at 48 and 72 hrs. Serum protein and globulin level showedan intial sharp increase from 2 to 20 hrs, followed by decline thatextend over a period of 72 hrs. Serum albumin showed an initialimmediate decline from 2 to 4 hrs, followed by an intermittent period of recovery and decline that extend over a period of 72hrs. Both lethal and sub-lethal concentrations of metal salts elicited asimilar pattern of response varying only in magnitude. The use offish blood serum protein, albumin and globulin measurements as general indicators of pollutant stress response isdiscussed.  相似文献   
44.
通过分析近40年来出现的ENSO事件对云南东川蒋家沟泥石流活动的影响可知,El Ni(~n)o与LaNi(~n)a对其的影响正好相反,且El Ni(~n)o的影响大于La Ni(~n)a的影响.El Ni(~n)o年,泥石流年发生频次、径流量和输沙量偏少的概率均较大,泥石流活动减弱的倾向明显;La Ni(~n)a年,虽有一定的对应关系,但不如El Ni(~n)o年明显,且影响更复杂一些,总的来说,泥石流年发生频次、径流量和输沙量偏多或持平的概率较大.  相似文献   
45.
Two Brassica species Brassica juncea and Brassica carinata of the Indian mustard, were grown in an artificially Ni-contaminated soil to study the tolerance and Ni accumulation. Chelating agent, EDTA was applied at the rosette stage for enhancing the metal uptake. Nickel concentration over almost double that in control was observed in both the species with Ni contamination along with EDTA application. Specie B. juncea appeared to be slightly more tolerant and higher accumulator of Ni. In agreement with the earlier reports, the translocation of the pollutant metal to the shoot from the root seemed to be restricted in both of Brassica species at higher rate of Ni application plus EDTA. The results of the present study indicated that B. juncea has the potential to be hyperaccumulator of Ni.  相似文献   
46.
生物炭和草酸活化磷矿粉对镉镍复合污染土壤的应用效果   总被引:5,自引:0,他引:5  
段然  胡红青  付庆灵  寇长林 《环境科学》2017,38(11):4836-4843
采用室内培养实验,利用生物炭和草酸活化磷矿粉对镉镍复合污染土壤进行修复,比较两者不同配比对土壤重金属镉镍的修复效果及对土壤无机氮和微生物量氮(MBN)转化的影响.结果表明,随着草酸活化磷矿粉和生物炭施用量的增加,土壤p H逐渐增加,镉和镍均由弱酸提取态逐渐向可还原态、可氧化态和残渣态转化,生物有效性降低.其中,C50P3(50 g·kg~(-1)生物炭与3 g·kg~(-1)草酸活化磷矿粉)配施的修复效果最好,弱酸提取态Ni占全量的质量分数降低了37.0%,残渣态Ni增加了14.8%,弱酸提取态Cd含量占全量的质量分数降低了40.2%,残渣态增加了35.2%.施用修复剂40 d后,相较于C0P0(空白对照)处理,C50P0(单施50 g·kg~(-1)生物炭)处理与C0P3(单施3 g·kg~(-1)草酸活化磷矿粉)处理微生物量氮含量均分别增加了1.5倍和1倍;铵态氮含量分别减少了12.5%和6.4%,硝态氮含量分别降低了11.6%和10.2%.综合比较可知,生物炭和草酸活化磷矿粉配施对土壤重金属镉镍复合污染的修复效果要优于单施,且50 g·kg~(-1)生物炭与3 g·kg~(-1)草酸活化磷矿粉(C50P3)配施的修复效果最好,修复剂的加入促进了土壤无机氮向有机氮的转化.  相似文献   
47.
采用微波消解-ICP-AES法测定底泥中的铜、镍等金属元素。通过实验和加标回收率的测定,回收率在88~102%之间。  相似文献   
48.
Zn/Ni/Cu-BTC强化吸附刚果红性能研究   总被引:1,自引:0,他引:1  
运用水热合成法制备了一种新型三金属单配体多孔材料Zn/Ni/Cu-BTC,运用氮气吸脱附、扫描电镜、X射线衍射等对材料进行了表征.研究了其常温常压条件下(25℃,1atm)静态吸附刚果红的性能.结果表明,由于三金属不饱和配位点的协同效应导致刚果红在Zn/Ni/Cu-BTC多孔材料上的吸附容量从630mg/g增加到1250mg/g,增加了98.4%.准二级动力学模型和Langmuir吸附模型较好地描述了Zn/Ni/Cu-BTC对刚果红的吸附行为.  相似文献   
49.
Herein,with the exploitation of iron and nickel electrodes,the 2,4-dichlorophenol(2,4-DCP)dechlorinating processes at the anode and cathode,respectively,were separately studied via various electrochemical techniques(e.g.,Tafel polarization,linear polarization,electrochemical impedance spectroscopy).With this in mind,Ni/Fe nanoparticles were prepared by chemical solution deposition,and utilized to test the dechlorination activities of 2,4-DCP over a bimetallic system.For the iron anode,the results showed that higher 2,4-DCP concentration and solution acidity aggravated the corrosion within the electrode.The charge transfer resistance(R_(ct))values of the iron electrode were 703,473,444,and 437Ω·cm~2 for the initial 2,4-DCP concentrations of0,20,50,and 80 mg/L,respectively.When the bulk pH of the 2,4-DCP solution varied from 3.0,5.0to 7.0,the corresponding R_(ct) values were 315,376,and 444Ω·cm~2,respectively.For the nickel cathode,the reduction current densities on the electrode at-0.75 V(vs.saturated calomel electrode)were 80,106,and 111μA/cm~2,for initial 2,4-DCP concentrations of 40,80,and125 mg/L.The dechlorination experiments demonstrated that when the initial pH of the solution was 7.0,5.0,and 3.0,the dechlorination percentage of 2,4-DCP by Ni/Fe nanoparticles was 62%,69%,and 74%,respectively,which was in line with the electrochemical experiments.10 wt.%Ni loading into Ni/Fe bimetal was affordable and gave a good dechlorination efficiency of 2,4-DCP,and fortunately the Ni/Fe nanoparticles remained comparatively stable in the dechlorination processes at pH 3.0.  相似文献   
50.
ICP-AES法测定煤矸石中的Ni、Fe、Mn、Cr   总被引:1,自引:0,他引:1  
取1.000g矸石样品于聚四氟乙烯坩埚中,加入5mLH2O2放置过夜,加6mL浓HCl,4mL浓HNO3,在微波炉中消解至近干,再加2mLHF,继续消解至粘稠状,用温热稀HCl溶解残渣,转入50mL容量瓶中,加1%HNO3定容,用ICP-AES法测定煤矸中Ni、Fe、Mn、Cr。在选定的测定条件下,检出限分别为0.013mg/L、0.0044mg/L、0.0014mg/L和0.0069mg/L;精密度的相对标准偏差分别为2.9%、3.4%、3.1%、2.1%;准确度实验铬的回收率在97.5%~106.0%之间。  相似文献   
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