沈阳市细河流域土壤重金属的暴露评估

在系统调查沈阳市细河流域土壤、农作物和大气降尘中重金属分布特征的基础上,按照美国环保局推荐的暴露模型和成人、儿童暴露参数,计算细河流域土壤中5种重金属Zn、Pb、Ba、Cd和Hg的成人、儿童暴露量。结果表明:污染土壤重金属的人群暴露主要来自食物途径,食物摄入暴露量明显大于呼吸摄入暴露量,皮肤接触暴露量则更小。5种金属的成人与儿童食物日暴露总量分别为0.121 mg/kg/d和0.185mg/kg/d,不同重金属的食物日暴露量为:Zn>Pb>Ba>Cd>Hg;呼吸与皮肤接触暴露中儿童的重金属暴露较成人明显,儿童与成人呼吸日摄入总量分别为1.01×10-2 mg/kg/d与1.08×10-3 mg/kg/d;皮肤接触暴露量分别为1.82×10-5 mg/kg/d与1.08×10-5 mg/kg/d。在3种暴露途径中,儿童的平均体重日暴露量均明显大于成人。

土壤有效态Pb和Cd与大蒜吸收Pb和Cd的关系

通过对大蒜的重金属添加土培试验,采用DTPA(二乙基胺五乙酸)为有效态铅、镉提取剂,对受试土壤进行浸提检测,分析Pb和Cd在大蒜不同部位的吸收、积累及其与土壤中有效态含量的相关性。根据GB 2762-2005《食品中污染物限量标准》中对食品中Pb、Cd的限量要求,初步确定了本试验条件下,土壤中重金属Pb、Cd有效态的临界值,并以此临界点评价该种土壤中Pb、Cd对大蒜的潜在污染。

污水灌溉对土壤重金属含量、酶活性和微生物类群分布的影响

以沈阳张士灌区长期污灌的农田土壤为对象,研究了土壤重金属、土壤酶活性、微生物生物量和种群分布特征,分析了土壤微生物参数与土壤重金属和土壤性质的相关关系。结果表明,虽然已停止污灌十余年,张士灌区农田土壤仍存在Cd、Zn、Cu等多种重金属污染。土壤Cd污染最严重,含量达1.75~3.89 mg.kg-1。土壤耕作层(0~30cm)Zn、Cu、Pb总含量随土层深度增加逐渐减少,而Cd元素的垂直分布呈向下迁移的趋势。Cd、Zn、Cu、Pb等4种重金属含量水平分布特征相似,均为1号样地>2号样地>3号样地>4号样地。相关性分析表明,张士灌区土壤酶活性、微生物生物量和种群分布受重金属污染和土壤养分的影响,土壤养分含量(有机碳、N、P、K)对微生物的正面效应大于重金属对微生物的负面效应。土壤全量Cd和速效K对微生物参数的影响最为明显,Cd含量与多酚氧化酶活性和微生物生物量(Cmic)呈极显著负相关,与纤维素酶活性呈极显著正相关(P<0.01),速效K含量与多酚氧化酶活性、微生物生物量以及可培养微生物种群数量均呈极显著正相关(P<0.01)。

易旱地区褐土P、Zn形态转化特点及其与持续农业的关系

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．

有机物料对滨海盐渍土重金属根际效应的影响Ⅰ.土壤内源Zn形态分布

研究了排水条件下施用腐熟有机物料、种稻改良滨海盐渍土内源Ｚｎ形态分布．结果表明，单淹水使土中各形态Ｚｎ一定程度上向生物有效性较低的Ｚｎ形态转化，有效态Ｚｎ降低．土壤盐分量不同，明显影响无定形氧化铁结合态、紧结有机态以及硅酸盐矿物态Ｚｎ变化．种稻不施有机物料，根际交换态和硅酸盐矿物态Ｚｎ亏缺；碳酸盐结合态、氧化锰结合态和无定形氧化铁结合态Ｚｎ富集．根际Ｚｎ形态转化强度大于非根际，其有效态Ｚｎ量接近临界值并高于非根际．有机物料利于根际内外土壤中硅酸盐矿物态Ｚｎ的转化，低盐土壤根际更强烈．随有机物料用量增加，促使根际硅酸盐矿物态、碳酸盐结合态及氧化锰结合态Ｚｎ向交换态、紧结有机态和无定形氧化铁结合态Ｚｎ转化，低盐土壤较明显．

热处理工艺对Mg-RE-Zn-Zr系合金显微组织及力学性能的影响

通过气体保护制备了Mg-RE-Zn-Zr[RE=Ce-40La(wt%)的富铈稀土]合金,并对合金进行了热处理,测试了不同状态下合金的硬度、抗拉强度及伸长率等力学性能,采用光学显微镜、X射线衍射仪及扫描电镜对合金显微组织、拉伸断口进行了分析。结果发现,采用T6热处理工艺后,合金的晶粒尺寸明显细化,硬度、抗拉强度、屈服强度和伸长率显著提高,分别提高了11%,24%,7.3%和102%

Synthesis and characterization of (Zn,Cd)TiO3 by a modified sol-gel method

Ilmenite-type (Zn1-xCdx)TiO3 (0 <= x <= 0.15 and 0.8 <= x <= 1.0) was synthesized by a modified sol-gel route including the Pechini process via two-step heat treatments. The thermal stability of (Zn1-xCdx)TiO3 depended on the amount of cadmium content. The as-synthesized (Zn1-xCdx)TiO3 (0 <= x <= 0.15 and 0.8 <= x <= 1.0) showed higher thermal stability than that of ZnTiO3. The variation of the dielectric constant of all synthesized (Zn1-xCdx)TiO3 samples for all measurement frequencies showed a similar tendency.

Stripping voltammetric determination of Pb(II) and Cd(II) based on the multiwalled carbon nanotubes-Nafion-bismuth modified glassy carbon electrodes

In this work, a new method for the simultaneous determination of Pb(II) and Cd(II) on the multiwalled carbon nanotubes (MWNT)-Nafion-bismuth modified glassy carbon electrode (GCE) using square-wave anodic stripping voltammetry has been studied. Scanning electron microscopy was used to investigate the characteristics of the MWNT-Nafion-bismuth modified GCE.

Sensitive determination of Cd and Pb by differential pulse stripping voltammetry with in situ bismuth-modified zeolite doped carbon paste electrodes

Here we investigated the analytical performances of the bismuth-modified zeolite doped carbon paste electrode (BiF-ZDCPE) for trace Cd and Pb analysis. The characteristics of bismuth-modified electrodes were improved greatly via addition of synthetic zeolite into carbon paste. To obtain high reproducibility and sensitivity, optimum experimental conditions for bismuth deposition Were Studied.

Constructing channel structures based on the assembly of p-sulfonatocalix[4]arene nanocapsules and [M(bpdo)(3)](2+)(M = Cu, Zn)

Novel channel structures based on [M(bpdo)(3)](2+) and p-sulfonatocalix[4]arene nanocapsules have been established; these are sustained exclusively by charge-assisted pi...pi interactions and sorption experiments show the porous materials have selective guest sorption properties.

The microstructures and mechanical properties of cast Mg-Zn-Al-RE alloys

The microstructures and mechanical properties of cast Mg-Zn-Al-RE alloys with 4 wt.% RE and variable Zn and At contents were investigated. The results show that the alloys mainly consist of alpha-Mg, Al2REZn2, Al4RE and tau-Mg-32(Al,Zn)(49) phases. and a little amount of the beta-Mg17Al12 phase will also be formed with certain Zn and At contents. When increasing the Zn or At content, the distribution of the Al2REZn2 and Al4RE phases will be changed from cluster to dispersed, and the content of tau-Mg-32(Al,Zn)(49) phase increased gradually. The distribution of the Al2REZn2 and Al4RE phases, and the content of beta- or tau-phase are critical to the mechanical properties of Mg-Zn-Al-RE alloys.

Theoretical studies on the reaction mechanism of oxidation of primary alcohols by Zn/Cu(II)-phenoxyl radical catalyst

The catalytic mechanism for the oxidation of primary alcohols catalyzed by the two functional models of galactose oxidase (GOase), M-II L (M = Cu, Zn; L = N,N'-bis(3,5-di-tert-butyl-2-hydroxyphenyl)1-2-diiminoquinone)), has been studied by use of the density functional method B3LYP The catalytic cycle of Cu- and Zn-catalysts consists of two parts, namely, substrate oxidation (primary alcohol oxidation) and O-2 reduction (catalyst regeneration). The catalytic mechanisms have been studied for the two reaction pathways (route 1 and route 2). The calculations indicate that the hydrogen atom transfer within the substrate oxidation part is the rate-determining step for both catalysts, in agreement with the experimental observation.

Synthesis and Characterization of One-Dimensional and Molecular M(tren)InAsS4 (M = Mn, Co, and Zn) Compounds with a Noncondensed AsS33- Unit

Four transition-metal-amine complexes incorporating indium thioarsenates with the general formula M(tren)InAsS4 (M=Mn, Co, and Zn) and a noncondensed AsS33- unit have been prepared and characterized. Single-crystal X-ray diffraction analyses show that compound 1 (M=Mn) crystallizes in the triclinic crystal system (space group: P (1) over bar) and consists of a one-dimensional (1D) inorganic (1)(infinity){[InAsS4](2-)} chain and [Mn(tren)](2+) groups bonded to the opposite sides of an eight-membered In2As2S4 ring along the backbone of the infinite inorganic chains. Compounds 2 (M=Mn), 3 (M=Zn), and 4 (M=Co) are isomorphous molecular compounds. They all crystallize in the monoclinic crystal system (space group: P2(1)/c). The Mn2+ cation of [Mn(tren)](2+) in 1 has a distorted octahedral environment, while the transition-metal cations of [M(tren)](2+) in the other three compounds locate in trigonal-bipyramidal environments.

The synthesis and properties of meso-tetra(4-alkylamidophenyl)porphyrin liquid crystals and their Zn complexes

A series of novel, long-chain-substituted, porphyrin derivatives, meso-tetra (4-alkylamidophenyl) porphyrin ligands and their Zn complexes (alkyl = 8,10,12,14,16,18) were prepared by acylation of the amino groups of 5,10,15,20-tetra(4-aminophenyl)porphyrin by alkyl chloride. Mesomorphism was investigated by DSC, polarized optical microscopy (POM) and X-ray diffraction (XRD). Only ligands containing chains > 12 carbon atoms displayed liquid crystalline behaviour, which exhibited a high phase transition temperature and a broad mesophase temperature span, Zn complexes showed no liquid crystalline behaviour. Cyclic voltammetry, luminescence spectra and surface photovoltage spectroscopy revealed that covalent linking of an alkylamido group to the tetraphenylporphyrin molecule influences, significantly, the properties of the porphyrin macrocycle.