利用地下水长观资料求解含水层参数

以银川平原灌区内的地下水动态观测资料,气象资料和灌溉试验资料为基础,分析了灌区内地下水的时空分布规律,并定量地确定了含水层参数:给水度度μ、潜水临界埋深△0、潜水蒸发系数C,采用此方法还可以推求降雨入渗补给系数a和灌溉回归系数等参数.     

碳酸钠浸取一紫外荧光光谱法测定地质样品中痕量铀

地质样品经HF-HNO_3-HCl-HClO_4溶解后,用50 g/L碳酸钠溶液浸取分离,采用紫外荧光光谱法直接测定上清液的铀含量。浸取时间选择30 min,Fe、Zn、Ca、Co、Ni、Cu和Mn等元素留在残渣中不产生干扰。方法精密度(RSD,n=12)为3．37%～7．06%,检出限为0．009μg/g(进样量100μL)。方法参加区域地球化学考核样品的测试,合格率100%,适用于土壤、水系沉积物、岩石及Fe、Zn、Ca、Co、Ni、Cu和Mn含量较高的样品中痕量铀的测定。     

Antimony in hydrothermal processes: solubility, conditions of transfer, and metal-bearing capacity of solutions

Based on data on the composition of ore-bearing hydrothermal solutions and parameters of ore-forming processes at various antimony and antimony-bearing deposits, which were obtained in studies of fluid inclusions in ore minerals, we investigated the behavior of Sb(III) in the system Sb–Cl–H₂S–H₂O describing the formation of these deposits.

We also performed thermodynamic modeling of native-antimony and stibnite dissolution in sulfide (m_HS⁻ = 0.0001−0.1) and chloride (m_Cl⁻ = 0.1−5) solutions and the joint dissolution of Sb_(s)⁰ and Sb₂S_3(s) in sulfide-chloride solution (m_HS⁻ = 0.01; m_Cl⁻ = 1) depending on Eh, pH, and temperature. All thermodynamic calculations were carried out using the Chiller computer program. Under the above conditions, stibnite precipitates in acid, weakly acid to neutral, and medium redox solutions, whereas native antimony precipitates before stibnite under more reducing conditions in neutral to alkaline solutions.

The metal-bearing capacity of hydrothermal solutions (200–250 °C) of different compositions and origins has been predicted. We have established that the highest capacity is specific for acid (pH = 2–3) high-chloride solutions poor in sulfide sulfur and alkaline (pH = 7–8) low-chloride low-sulfide solutions.     

缺陷化学在新材料研究中的作用

简述了缺陷的类型及其在新材料制备中的作用,通过实例分析固溶体和非化学计量化合物缺陷对材料物理化学性能的影响,阐明缺陷化学是一种研究新型功能材料的有力手段,根据新材料的发展趋势分析了缺陷化学可能取得的重大突破及新的研究热点。     

古玉器的化学风化机理初探之二——块状模拟实验

在前文粉末态模拟实验基础上,初步模拟古玉埋藏的酸性以及碱性环境,通过对不同材质玉料的块状形态在酸、碱缓冲溶液中的浸泡实验,并与粉末态玉料的浸泡结果进行对比分析,以深化对古玉器风化机理的认识。     

Evidence for kinks in structural and thermodynamic properties across the forsterite–fayalite binary from thin-film IR absorption spectra

Infrared absorbance spectra over ∼100 to 1,800 cm⁻¹ were collected from optically thin films of 21 samples with compositions spanning the forsterite–fayalite binary. Polarization information from previous specular reflectance data on end-members was used in tracing the peaks across the entire binary. Peak positions (ν_i) were constrained by Lorentzian decompositions. Fitting also constrained widths for singlet peaks but for doublets and triplets, variation in ν_i with composition among the constituent polarizations alters widths from intrinsic. Because film thicknesses of 0.6–1.4 μm were estimated, our band strengths are approximate; however, relative intensities should be correct. Only for a few peaks does ν_i vary smoothly across the entire binary; instead, distinct linear trends exist for Fe- and Mg-rich olivines. Discontinuities and kinks in ν_i(X) occur at X = Mg/(Fe + Mg) = 0.7 and are accompanied by a change in intensity patterns. This interesting behavior was not revealed in previous spectra of powder dispersions. The contrasting character of IR vibrations for Fe- and Mg-rich olivines is inferred to arise from structural variations because (1) frequency is related to bond length, (2) other factors affecting frequency (cation mass and probably bonding type) vary linearly across the binary, and (3) available data on unit cell parameters are consistent with distinct trends for forsterites and fayalites. Vibrational components of heat capacity (C _V) and enthalpy (H) calculated from ν_i, were found to be slightly more negative than linear interpolations between values for forsterite and fayalite. Our computations give smaller negative excesses from ideality in H than do previous calorimetric measurements, but are equal within experimental uncertainties.     

Effects of orientation on the diffusive properties of fluid-filled grain boundaries during pressure solution

An unresolved issue in the study of pressure solution in rock materials is the dependence of grain boundary structure and diffusive properties on the mutual orientation of neighbouring grain lattices. We report electrical measurements yielding the diffusivity of differently oriented halite–glass and halite–halite contacts loaded in the presence of brine. The halite–glass contact experiments show pressure solution of the halite and an effect of halite lattice orientation on grain boundary transport. Post-mortem observations show an orientation-dependent grain boundary texture controlled by the periodic bond chains in the halite structure. It is inferred that this texture determines the internal grain boundary structure and properties during pressure solution. In the halite–halite experiments neck-growth occurred, its rate depending on twist-misorientation. The results imply that deformation by pressure solution may lead to lattice-preferred orientation development, and that polymineralic rocks may deform faster at lower stresses than monomineralic rocks.     

Thermodynamics of mixing in diopside–jadeite,CaMgSi<Subscript>2</Subscript>O<Subscript>6</Subscript>–NaAlSi<Subscript>2</Subscript>O<Subscript>6</Subscript>, solid solution from static lattice energy calculations

Static lattice energy calculations (SLEC), based on empirical interatomic potentials, have been performed for a set of 800 different structures in a 2 × 2 × 4 supercell of C2/c diopside with compositions between diopside and jadeite, and with different states of order of the exchangeable Na/Ca and Mg/Al cations. Excess static energies of these structures have been cluster expanded in a basis set of 37 pair-interaction parameters. These parameters have been used to constrain Monte Carlo simulations of temperature-dependent properties in the range of 273–2,023 K and to calculate a temperature–composition phase diagram. The simulations predict the order–disorder transition in omphacite at 1,150 ± 20°C in good agreement with the experimental data of Carpenter (Mineral Petrol 78:433–440, 1981). The stronger ordering of Mg/Al within the M1 site than of Ca/Na in the M2 site is attributed to the shorter M1–M1 nearest-neighbor distance, and, consequently, the stronger ordering force. The comparison of the simulated relationship between the order parameters corresponding to M1 and M2 sites with the X-ray refinement data on natural omphacites (Boffa Ballaran et al. in Am Mineral 83:419–433, 1998) suggests that the cation ordering becomes kinetically ineffective at about 600°C.     

大别造山带毛屋超镁铁岩的铂族元素研究

采用镍锍火试金法结合ICP-MS分析了毛屋斜方辉石岩和石榴二辉岩样品中的Ir、Ru、Rh、Pt和Pd的含量,结果显示其铂族元素(PGE)的含量随岩石类型无规律性的变化,原始地幔标准化后的铂族元素分布模式呈负斜率,Pd、Ir发生了分异。毛屋超镁铁岩铂族元素特征的形成受岩石中铂族元素的存在相制约,PPGE富集在富Cu硫化物,而IPGE以类似残留相、不熔的单硫化物固熔体形式存在,其中地壳混染也起了一定的作用;同时,成岩过程中流体的存在造成了Pt和Pd的活化。因此,单硫化物固熔体和流体的共同作用形成了毛屋超镁铁岩类似残留地幔岩的铂族元素分布特征。