386 resultados para Ni-Zn ferrite


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通过添加不同比例的粉煤灰对城市生活污泥进行钝化,系统的研究了粉煤灰对钝化污泥中金属元素Cd、Pb、Cu、Zn、Ni、Cr、Mn、Fe含量及其有效化的影响。结果表明:粉煤灰对污泥中有效态Cd、Pb、Ni、Cr、Mn、Fe具有钝化作用,其中对Cd和Fe的钝化效果最明显;但对Cu却有促进其向有效态转化的作用;总体上看钝化污泥人工土壤中重金属含量符合国家农用标准,而其中有效态Cd、Pb、Ni、C r的含量均远远低于对植物体造成毒害的临界水平。

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通过添加不同比例的粉煤灰对城市污泥进行钝化,对钝化污泥的pH值、养分含量及重金属含量变化以及各配比人工土壤的持水性能进行了研究,评价其用于无土排岩场生态修复的可行性.结果表明,当粉煤灰与污泥以Ⅲ(1∶1)和Ⅱ(2∶1)配比时,人工土壤持水性能高于对照(草甸棕壤),以Ⅳ(1∶2)配比时,持水性接近于对照;粉煤灰钝化污泥中养分含量极其丰富,处于高肥力水平,随着粉煤灰添加量的增加,人工土壤的养分含量呈现降低趋势;粉煤灰钝化污泥人工土壤中除了Ⅲ(1∶1)中Ni含量较高,为187.67 mg.kg-1外,各处理中重金属Cd、Pb、Cu、Zn、Cr含量都显著低于国家农用标准(GB 4284-84、GB 8173-87).

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The selective catalytic reduction (SCR) of NOx by methane in the presence of excess oxygen was studied on a Zn-Co/HZSM-5 catalyst. It was found that the addition of Zn could improve effectively the selectivity of methane towards NOx reduction. When prepared by a coimpregnation method, the Zn-Co/HZSM-5 catalyst showed much higher catalytic activity than the two catalysts of a Zn/Co/HZSM-5 and Co/Zn/HZSM-5 prepared by the successive impregnation method. It is considered that there exists a cooperative effect among the Zn, Co and zeolite, which enhances the reduction of NO to NO2 reaction and the activation of methane. (C) 2002 Elsevier Science B.V. All rights reserved.

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A method has been developed for the determination of interactions of metal ions and protein by using microdialysis sampling technique combined with pre-column derivation and reversed-phase ion-pair liquid chromatographic (HPLC analysis. Cu(II), Zn(II) and human serum albumin (HSA) were chosen as model metal ions and protein, respectively. The mixed solutions of metal ions and HSA with different molar ratios buffered with 0.1 M Tris-HCl containing 0.1 M NaCl at pH 7.43 were sampled with a mirodialysis probe by keeping perfusion rate at 1 mul/min and the temperature at 37 degreesC. The free concentrations of metal ions in microdialysates were assayed by precolumn derivatization with meso-tetra(4-sulfophenyl)-porphyrin (TPPS4) followed ion-pair HPLC analysis. The recovery (R) of microdialysis sampling was measured in vitro under similar conditions as 65.74% for Cu(II), 70.45% for Zn(II) with R.S.D. below 3.2%. The primary binding constants and number of binding site estimated by the Scatchard plot analysis are 5.04 x 10(6) M-1 and 0.85 for Cu(II), and 9.87 x 10(6) M-1 and 1.10 for Zn(II), respectively. The competition of Cu(II) and Zn(II) at the second binding site on HSA was investigated, and it was observed that there is a second site on HSA to bind Cu(II) and Zn(II), the affinity of Cu(II) is stronger than that of Zn(II) to this second site of HSA. (C) 2001 Elsevier Science B.V. All rights reserved.

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“Dissolved” (< 0.4 μm filtered) and “total dissolvable” (unfiltered) trace element samples were collected using “clean” sampling techniques from four vertical profiles in the eastern Atlantic Ocean on the first IOC Trace Metals Baseline expedition. The analytical results obtained by 9 participating laboratories for Mn, Fe, Co, Ni, Cu, Zn, Cd, Pb, and Se on samples from station 4 in the northeast Atlantic have been evaluated with respect to accuracy and precision (intercomparability). The data variability among the reporting laboratories was expressed as 2 × SD for a given element and depth, and was comparable to the 95% confidence interval reported for the NASS seawater reference standards (representing analytical variability only). The discrepancies between reporting laboratories appear to be due to inaccuracies in standardization (analytical calibration), blank correction, and/or extraction efficiency corrections.Several of the sampling bottles used at this station were not adequately pre-cleaned (anomalous Pb results). The sample filtration process did not appear to have been a source of contamination for either dissolved or particulate trace elements. The trace metal profiles agree in general with previously reported profiles from the Atlantic Ocean. We conclude that the sampling and analytical methods we have employed for this effort, while still in need of improvement, are sufficient for obtaining accurate concentration data on most trace metals in the major water masses of the oceans, and to enable some evaluation of the biogeochemical cycling of the metals.

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The sorption on humic acid (HA) of metals from an aqueous solution containing Hg(II). Fe(III), Pb, Cu, Al, Ni, Cr(III), Cd, Zn, Co and Mn, was investigated with special emphasis on effects of pH, metal concentration and HA concentration. The sorption efficiency tended to increase with rise in pH, decrease in metal concentration and increase in HA concentration of the equilibrating solution. At pH 2.4. the order of sorption was: Hg Fe Pb Cu=Al Ni Cr=Zn=Cd=Co=Mn. At pH 3.7. the order was: Hg and Fe were always most readily removed, while Co and Mn were sorbed least readily. There were indications of competition for active sites (CO2H and phenolic OH groups) on the HA between the different metals. We were unable to find correlations between the affinities of the eleven metals to sorb on HA and their atomic weights, atomic numbers, valencies, and crystal and hydrated ionic radii. The sorption of the eleven metals on the HA could be described by the equation Full-size image (1K), where Y = % metal removed by HA; X = mgHA; and A and B are empirical constants

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【目的】研究山杏种皮黑色素与Cu2+和Zn2+络合的相关性质,为山杏种皮黑色素以及其他植物黑色素的开发利用提供依据。【方法】采用电位滴定、紫外-可见光差示吸收光谱和红外光谱对山杏种皮黑色素与Cu2+和Zn2+的络合物进行分析。【结果】Cu2+和Zn2+与山杏种皮黑色素络合后,均能促进山杏种皮黑色素酸性位点的去质子化作用,但Cu2+的促进作用更强,结合更为牢固;随pH值升高,山杏种皮黑色素中解离出的络合位点增多,络合Cu2+能力增强。【结论】Cu2+和Zn2+主要与山杏种皮黑色素中羰基发生络合作用,氨基和羟基参与了络合。

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利用地统计学方法研究了沈阳市细河流域表层土壤中Hg、Cd、Pb和Zn含量的空间结构及其分布特征。结果表明,土壤中Hg、Cd、Pb和Zn的平均含量均高于其背景值;土壤Cd和Zn含量属中等程度的空间相关,Hg和Pb属于空间弱相关,其空间变异均为随机性因素和结构性因素共同作用的结果,但Cd和Zn含量主要受结构性因素影响,而Hg和Pb主要受随机性因素影响。土壤中Hg、Cd、Pb和Zn空间分布特征表明,4种重金属含量在上游较高,顺流而下含量明显下降;土壤中Hg和Pb含量最大值在四方台地区,Cd和Zn含量最大值分布在甘官和富官一带。细河流域土壤Hg、Cd、Pb和Zn含量空间分异是污水灌溉、固体废弃物堆放、农业生产及交通尾气等因素综合作用的结果。

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采用田间微区试验和分级提取测定的方法研究了褐土中P、Zn形态转化问题.发现褐土中Ca2-P和Ca8-P是转化最活跃的P素形态.而且Ca8-P的流通容量很大,可超过作物需P量9倍以上;在Zn的各种形态中转化最活跃的是EX-Zn和CARB-Zn,其中CARB-Zn的流通容量亦很大,可超过作物需Zn量19倍以上.Ca8-P库和CARB-Zn库形成了褐土中调控P、Zn养分供蓄以适应旱地水分波动的主要机构.合理施肥和培肥土壤以丰富Ca8-P和CARB-Zn库将有利于增强作物抵御干旱能力,提高水分养分利用效率,促使旱地农业持续向高产优质高效方向发展.