凹凸棒石与Zn^2＋的长期作用研究

以凹凸棒石与Zn2＋为例研究粘土矿物与重金属离子长期作用过程,并运用高分辨透射电镜和X射线衍射分析粘土矿物与重金属离子长期作用的次生物相。结果表明：Zn2＋与凹凸棒石的长期作用是一个二阶段的过程,初始阶段为快速吸附作用,其后表现为慢速沉淀反应。高分辨透射电镜和X射线衍射分析表明,凹凸棒石与Zn2＋的长期作用过程中,具有纳米矿物特性的凹凸棒石表面快速水化,提高了悬浮液的pH值,诱导Zn2＋水解沉淀。而后,凹凸棒石缓慢溶解释放Al3＋和SiO44-与Zn（OH）2沉淀反应,形成Zn-A1双氢氧化物和异极矿。这一结果对认识土壤环境中重金属与粘土矿物的作用及重金属的归宿具有重要意义。     

Influence of the water layer upon the depth of ground radar investigations in freshwater reservoirs

A number of problems associated with detailed investigation of subsurface geological structure below the bottoms of freshwater reservoirs (rivers, ponds, and lakes) arise during the study of the upper portions of geological sections. The present study is aimed at marginal estimation of the penetrating depth of ground radar investigations in freshwater reservoirs (based on bottom reflections), taking into account the complex nature of conductivity and its dependence upon the frequency under ideal conditions with no noise. The same method can be applied for estimating any given dynamic recording range.     

不同超富集、富集植物-玉米间作模式对玉米中镉吸收、转运的影响研究

为了研究Cd污染条件下,玉米分别与苋菜、黑麦草、龙葵间作对重金属Cd吸收和转运的特点,从而选择适宜与玉米间作的富集植物,同时达到修复重金属Cd污染土壤的目的。该文以镉(Cd)污染的河南棕壤黏土为供试土壤,通过盆栽试验,基于玉米各器官中Cd含量、富集系数、转运系数、土壤有效态Cd含量的变化,研究了间作苋菜、黑麦草、龙葵对玉米各器官Cd的积累特性的影响及其迁移转运机制。结果表明：(1)龙葵、苋菜、黑麦草间作使得玉米地上部Cd含量显著性降低(P<0.05),其中以籽粒中Cd含量的下降最为显著。间作苋菜、黑麦草、龙葵,玉米籽粒中Cd含量分别下降了67.6%、75.7%和79.9%。(2)间作苋菜、黑麦草、龙葵使得玉米的富集系数较单作处理下玉米的富集系数分别下降了49.3%、39.7%和68.5%,且差异达到显著水平。(3)与苋菜、黑麦草间作相比,间作龙葵的玉米转运系数分别下降了27.5%、24.2%,且差异均达到显著水平。通过对人体每天摄入Cd量的安全值计算得出间作后土壤中Cd全量应低于2.26 mg·kg-1,土壤有效态Cd含量低于0.88 mg·kg-1。该污染农田在间作模式下,食用玉米Cd暴露对居民健康不存在风险。间作苋菜、黑麦草、龙葵能够抑制玉米对Cd的吸收,同时阻控玉米地上部Cd向地上部的转移,尤其是向籽粒转移。通过间作苋菜、黑麦草、龙葵,不仅降低了主栽作物玉米的Cd累积量,实现玉米安全、优质种植,同时也达到了修复污染土壤的目的。     

地质勘查阶段煤系石墨与无烟煤的划分指标探究

煤系石墨是煤及煤系炭质页岩在岩浆热接触变质及构造变质作用下形成的,是石墨矿产的重要组成部分,属新兴战略资源。目前由于对煤系石墨赋存规律认识不清,缺乏科学界定的勘查指标,以致造成了严重浪费。在总结以往划分煤系石墨与无烟煤的思路和方法基础上,以吉林磐石、湖南鲁塘、福建西南等典型煤系石墨与无烟煤样品测试结果为依据,分析了煤系石墨有关参数的优缺点,提出采用H/C原子比、晶格间距d₀₀₂、拉曼光谱R₂ 3个参数,作为勘查阶段界定煤系石墨与无烟煤的定量指标。     

Fe3+纳米胶体颗粒的光吸收边蓝移与溶液中Al/Fe比的关系

合成了n（Al）／n（Fe）和碱化度不同的45个聚合氯化铝铁（PAFC）样品,进行了光谱分析,结果显示光吸收边蓝移或红移以及Fe（Ⅲ）羟基氧化物和Al-Fe共聚体纳米胶体颗粒大小分布与溶液的Al／Fe比和碱化度（B=[OH]／[Al＋Fe]）密切相关。电镜观察和电子衍射分析表明：Al（Ⅲ）的加入使Fe（Ⅲ）羟基氧化物和Al-Fe共聚体纳米胶体颗粒变小、有序度降低是造成PAFE光吸收边蓝移和保持胶体颗粒在亚稳定状态下存在的重要原因。当n（Al）／n（Fe）〉8：2后,PAFC溶液中Fe（Ⅲ）羟基氧化物和Al-Fe共聚体胶体主要以〈10m的纳米颗粒形态存在,对应的光谱能级提高到26000cm^-1以上,且各种曰值下Fe^3＋的光谱能级趋于一致。这表明,在大量Al（Ⅲ）存在条件下,PAFE中Fe3^＋的所处的化学环境相似。点能谱分析显示,n（Al）／n（Fe）=4：6的样品中颗粒物的化学计量比最接近AlOOH,FeOOH,溶液的稳定性最差。     

伊利石层间钾释放的远红外光谱研究

本文介绍了新近研究层间交换的远红外方法，并用该方法研究了金砂伊早石层间交换的性质，随着温度的升高，伊利石的远红外谱段从１０８ｃｍ＾－１向低波数方向偏移，３００Ｃ时为１０７ｃｍ＾－１，５００℃时为１０００ｃｍ＾－１，７００℃时为９８ｃｍ＾－１，同时，伊利石的释钾程度也伴随着增加，远红外谱同释放钾的能力有一清楚对比，因此可以用远红外方法预言伊利石释钾的能力，最后，利用量子化学计算的ＰＭ３方法首次从理论     

氯化钠存在下氯化亚锡—罗丹明B—水体系浮选分离铱

研究了Ir（Ⅲ）在NaCl存在下SnCl2－罗丹明B－水体系中的浮选行为，在1.0mol/L HCl介质中，Ir（Ⅲ）与Pd,Pt,Rh,Au同时被浮选，Ir（Ⅲ）的浮选率为99.2％，并与常见贱金属离子分离，被浮选分离的Ir可采用原子吸收法测定，结果与火试金分离富集法相符。精密度试验，相对标准偏差（RSD，n＝5）＜3％。     

铋的原子吸收光谱分析进展

文章对１９８５年以来用原子吸收光谱法测定Ｂｉ的情况进行了综述,着重介绍了用氢化物发生法、石墨炉法和火焰法测Ｂｉ时,为了提高灵敏度所采用的各种氢化物发生装置及根据不同试样所使用的各种分离富集手段。主要参考文献１０１篇。     

Mössbauer effect study of anapaite, Ca2Fe2+(PO4)2 · 4H2O, and of its oxidation products

Mössbauer spectra (MS) of anapaite (Ca₂ Fe²⁺(PO₄)₂?·?4H₂O) and of a sample after being immersed in a 4% H₂O₂ solution at room temperature (RT) over 12 days (hereafter an4ox) were collected at temperatures in the range 4.2 to 420?K and 11 to 300?K respectively. All MS consist of symmetrical doublets, hence magnetic ordering was not observed. The temperature dependencies of the Fe²⁺ centre shifts of anapaite and an4ox were analysed with the Debye model for the lattice vibrations. The characteristic Mössbauer temperatures were found as 370?K?±?25?K and 340?K?±?25?K, and the intrinsic isomer shifts as 1.427?±?0.005?mm/s and 1.418?±?0.005?mm/s respectively. From the external-field (60?kOe) MS recorded at 4.2 and 189?K for the non-treated sample, the principal component V _zz of the electric field gradient (EFG) is determined to be positive and the asymmetry parameter η?≈?0.2 and 0.4 respectively. The temperature variations of the quadrupole splittings, ΔE _Q(T), cannot be interpreted on the basis of the thermal population of the ⁵ D electronic levels resulting from the tetragonal compression of the O₆ co-ordination. The low-temperature linear behaviour of ΔE _Q(T) is attributed to a strong orbit-lattice coupling. A field of 60 kOe applied to anapaite at 4.2?K produces magnetic hyperfine splitting with effective hyperfine fields of ?136, ?254 and ?171?kOe along the principal axes Ox, Oy and Oz of the EFG tensor respectively. Additional oxidation treatments in solutions with various H₂O₂ concentrations up to 20% and subsequent Mössbauer experiments at room temperature, have revealed that the anapaite structure is not sensitive to oxidation since eventually only a small amount of Fe²⁺ (～6.5%) is converted into Fe³⁺.     

Intracrystalline fractionation of Fe in synthetic (Fe, Mg, Zn) - bearing staurolite: a Mössbauer spectroscopic study

⁵⁷Fe-Mössbauer spectra of eleven Fe-Mg-bearing staurolite samples, synthesized at 5, 20 and 25 kbar and 680°C, ranging in composition from x_Fe?=1.00 to x_Fe?=0.15, and of two Zn-Fe-bearing staurolite samples, synthesized at 20 kbar and 700°C with x_Fe?=0.10 and x_Fe?=0.32 were collected at room temperature. The spectra reveal that about 80% of Fe_tot (in case of Fe-Mg-bearing staurolite) and about 70% of Fe_tot (in case of Fe-Zn-bearing staurolite) are located as Fe²⁺ at the three subsites Fe1, Fe2 and Fe3 of the tetrahedral T2-site. The refinement of the spectra results in almost identical values for the isomer shift (IS) (±1.0 mm/s) but significantly different values for the quadropole splitting (QS) for the three subsites which is in accordance with the different distortions of these sites. About 8% of Fe_tot (in case of Fe-Mg-bearing staurolite) and 13% of Fe_tot (in case of Fe-Zn-bearing staurolite) are located as Fe²⁺ at the octahedral M4 site, while the remainder percents of Fe_tot indistinguishably occur as Fe²⁺ at the octahedral M1 and M2 sites of the kyanite-like part of the structure. Within the whole Fe-Mg-staurolite solid solution series the Mössbauer parameters QS of the sites M4 and (M1, M2) vary systematically with composition whereas IS remains constant. There is a high negative correlation of the total Mg-content with Fe-occupation of all the Fe-bearing sites indicating a continuous substitution of Fe²⁺ by Mg on all these sites. Synthetic Fe-staurolites show no increasing occupation of the octahedral sites by two-valent cations with pressure, as was assumed by several authors.