长白山天池火山千年大喷发岩浆含水量研究——熔融包裹体含水量的红外光谱测试

长白山天池火山在公元一千年左右曾发生过大规模喷发,其产物为大面积分布的灰白色碱流质浮岩和碎屑流,在其斑晶矿物橄榄石、钙铁辉石和碱性长石中均可见到熔融包裹体。在最主要的斑晶矿物——碱性长石中含有数量众多且个体也较大的熔融包裹体,多数含有一个以上的气泡,其中部分含有子晶,根据形貌特征的不同可分为截然不同的两组包裹体。这些熔融包裹体带有大量喷发前地下岩浆的信息,成为研究地下深部的岩浆在复杂的溢流-爆炸喷发中所发生变化的最好媒介。也是本文的研究对象,通过其中挥发份尤其是水的含量,可以推知天池火山发生大喷发的原因。经Nicolet Magna-IR 550红外光谱仪测定,这些熔融包裹体的含水量较高,达1．6％-3．6％,为当时天池火山发生了巨大规模爆炸喷发的原因提供了强有力的证据。但目前红外光谱仪的应用范围还比较有限,有待今后拓宽其应用领域。     

FTIR characterization of amorphous uranyl-silicates

Ambient-temperature environments in which dissolved silica and U(VI) are present may lack the conditions necessary to readily form crystalline uranyl-silicate phases; however amorphous phases, as defined by the absence of well-defined Bragg reflections in powder X-ray diffraction patterns, are kinetically favored when solution saturation levels are appropriate. Such amorphous uranyl-silicates may be related to the crystalline phases predicted to be thermodynamically stable and influence the mobility of U in the environment. To investigate amorphous uranyl-silicates and their relation to crystalline phases we precipitated solids from solutions containing 0.05 M UO₂(ClO₄)₂ and 0.1 M Na₂SiO₃ adjusted to pH values from 2.2 to 9 and allowed the precipitates to age in their mother liquors for approximately 6 weeks at 22 °C. We compared the chemical composition, X-ray diffraction patterns, and Fourier transform infrared spectra of the precipitates to those of the crystalline phases predicted by thermodynamic modeling. The precipitates were amorphous with U:Si ratios of 0.8 ± 0.1. Their FTIR spectra revealed changes in the UO₂²⁺ and SiO₄⁴⁻ vibrations as a function of pH that are consistent with a shift in mid-range structural linkages from those similar to soddyite to those more like Na-boltwoodite. Structural H₂O, OH, and SiO₃OH³⁻ vibrations do not change as a function of pH and are consistent with a mixture of soddyite-like and Na-boltwoodite-like features. Six weeks of aging at ambient temperature is enough time for the precipitate structures to rearrange and adopt mid-range structural linkages characteristic of crystalline phases predicted by thermodynamic modeling.     

Vibrational Spectroscopic Study for Qualitative Assessment of Mn‐oxide Ore

Manganese oxide ore from the Bonai‐Keonjhar belt of Odisha, India, has been qualitatively assessed through Raman and FTIR spectroscopy, and X‐ray diffraction. Three categories of ore, namely, high‐grade (MnO₂: >72%), medium‐grade (MnO₂: 55‐72%) and low‐grade (MnO₂:40‐55%) from four mine profiles, Purnapani, Joda West, Khandbandh and Bamebariwere, were collected and subjected to vibrational spectroscopic studies. The use of Raman analysis in the microscopic configuration allowed the spectra to be taken at different points on the polished ore. Besides the Raman features of the ß‐MnO₂(Pyrolusite) phases, other signals were assigned to isolated FeO ions accommodated in vacancies and to some aluminium silicates. The three grades of ore show different Raman spectra. The FTIR spectra also exhibit contrasting pattern in different grade sample and support these findings. This study demonstrates the use of vibrational spectroscopy to assess the quality of Mn‐oxide ore that could provide a substitute to cumbersome wet chemical analysis     

大陆下地壳和岩石圈地幔含水性的差异——山东莒南玄武岩中深源包体的初步观察

对产于莒南晚中生代玄武岩中的镁铁质麻粒岩和橄榄岩包体矿物进行了傅里叶变换红外光谱(FTIR)分析.结果显示,麻粒岩矿物和全岩中水含量分别为:单斜辉石300×10-6～1 180×10-6,斜方辉石80×10-6～169×10-6,斜长石717×10-6～1 239×10-6,全岩525×10-6～855×10-6;橄榄岩矿物和全岩中水含量分别为:单斜辉石466×10- 6～746×10-6,斜方辉石187×10-6～304×10-6,橄榄石6×10-6～15×10-6,全岩81×10-6～245×10-6.从单矿物看,麻粒岩和橄榄岩之间水含量的差距不是很明显,但麻粒岩的全岩水含量明显高于橄榄岩,表明大陆深部岩石圈的水含量在垂向上具有不均一性.     

下地壳含水性的演化 ——来自不同时代麻粒岩中长石水含量的证据

利用傅里叶变换红外光谱(FTIR)和电子探针(EMP)分析了早古生代的松树沟麻粒岩和桐柏麻粒岩地体以及古元古代的莒南麻粒岩包体(其寄主岩石为新生代玄武岩)中长石的水含量和化学成分。结果显示,麻粒岩中的长石均含有以OH和H2O形式存在的结构水;3个地点的长石水含量分别为465×10-6~733×10-6、210×10-6~993×10-6和717×10-6~1 239×10-6。对比前人报道的中生代(道县和汉诺坝包体)和古元古代(女山包体、汉诺坝地体)的麻粒岩研究结果,发现早古生代样品和古元古代样品中长石的水含量都比中生代样品明显的高,而早古生代和古元古代样品之间却没有差别,指示了中国东部下地壳在中生代之前更加富水。     

Assessment and characterization of heavy metal resistance in Palk Bay sediment bacteria

The present study aimed at characterizing the heavy metal resistance and assessing the resistance pattern to multiple heavy metals (300 mmol L?1) by Palk Bay sediment bacteria. From 46 isolates, 24 isolates showed resistance to more than eight heavy metals. Among the 24 isolates S8-06 (Bacillus arsenicus), S8-10 (Bacillus pumilus), S8-14 (B. arsenicus), S6-01 (Bacillus indicus), S6-04 (Bacillus clausii), SS-06 (Planococcus maritimus) and SS-08 (Staphylococcus pasteuri) exhibited high resistance against arsenic, mercury, cobalt, cadmium, lead and selenium. Plasmid curing confirmed that the heavy metal resistance in S8-10 is chromosomal borne. Upon treatment with the heavy metals, the strain S8-10 showed many morphological and physiological changes as shown by SEM, FTIR and AAS analysis. S8-10 removed 47% of cadmium and 96% of lead from the growth medium. The study suggests that sediment bacteria can be biological indicators of heavy metal contamination.     

A Study: Removal of Cu(II), Cd(II), and Pb(II) Ions from Real Industrial Water and Contaminated Water Using Activated Sludge Biomass

This study aims to remove of Cu²⁺, Cd²⁺, and Pb²⁺ ions from solution and to investigate the adsorption isotherms, adsorption kinetics, and ion‐exchange affinities of these metals using waste activated sludge (AS) biomass. The adsorptions of the metals on biomass were optimal at an acidic pH value of 6.0 based on its monolayer capacities. Maximum monolayer capacities of AS biomass (q_max) were calculated as 0.478, 0.358, and 0.280 mmol g^?1 for Cu²⁺, Cd²⁺, and Pb²⁺, respectively, and the adsorption equilibrium time was found as 60 min for each metal. The adsorbed amount of metal rose with increasing of initial metal ion concentration. The equilibrium adsorption capacity of AS for initial 0.25 mmol L^?1 metal concentration was determined as 0.200, 0.167, and 0.155 mmol g^?1 for Cu²⁺, Cd²⁺, and Pb²⁺ ions, respectively. These relevant values were determined as 0.420, 0.305, and 0.282 mmol g^?1 for Cu²⁺, Cd²⁺, and Pb²⁺ ions, respectively, when initial metal concentration was 0.50 mmol L^?1. In the multi‐metal sorption system, the adsorption capacity of AS biomass was observed in the order of Cu²⁺ > Cd²⁺ > Pb²⁺. In the presence of 100 mmol L^?1 H⁺ ion, the order of ion‐exchange affinity with H⁺ was found as Cu²⁺ > Cd²⁺ > Pb²⁺. The adsorption kinetics were also found to be well described by the pseudo‐second‐order and intraparticle diffusion models. Two different rate constants were obtained as k_i1 and k_i2 and k_i1 (first stage) was found to be higher than k_i2 (second stage).     

富镁和贫镁坡缕石及其酸浸蚀产物的红外吸收光谱研究

本文对两个富镁和贫镁坡缕石的红外吸收光谱高频区的拟合结果表明,富镁坡缕石(p0)和贫镁坡缕石(g0)的八面体离子的配置有区别,前者除出现Mg3OH振动外,MgM2口OH振动的比例比AlM2口OH振动的大,后者则反之。经酸短时间浸蚀的和未经浸蚀的坡缕石红外吸收光谱相比,除部分吸收峰(如3560cm^-1)的峰形发生明显变化外,其余各吸收峰的峰形相似、强度稍有变化,且Siu-O-SiD的不对称振动吸收峰向低波数方向偏移、对称吸收峰向高波数方向偏移;坡缕石中790cm^-1左右的吸收峰的归属是不明确的,据实验确认它是由Siu-O-SiD的对称吸收所致;由985cm^-1、1030cm^-1、1080cm^-1和1200cm^-1左右4个吸收峰组成Si-O骨架振动吸收带的峰形、强度和峰位移反映了酸浸蚀过程中坡缕石的结构改变。两个坡缕石经360h盐酸浓度为1mol／L和3mol／L浸蚀后,所得产物的粉末X射线衍射谱虽仍具有坡缕石的衍射线,但它们的红外吸收光谱却只有与表面OH振动、物理吸附水相关的OH振动和几个SiO振动吸收峰,而无代表八面体振动、硅氧骨干中的大部分SiO振动和晶格中的结晶水的振动,说明酸对坡缕石浸蚀的最后产物是以硅氧为主。     

Diffusion-controlled spherulite growth in obsidian inferred from H<Subscript>2</Subscript>O concentration profiles

Spherulites are spherical clusters of radiating crystals that occur naturally in rhyolitic obsidian. The growth of spherulites requires diffusion and uptake of crystal forming components from the host rhyolite melt or glass, and rejection of non-crystal forming components from the crystallizing region. Water concentration profiles measured by synchrotron-source Fourier transform spectroscopy reveal that water is expelled into the surrounding matrix during spherulite growth, and that it diffuses outward ahead of the advancing crystalline front. We compare these profiles to models of water diffusion in rhyolite to estimate timescales for spherulite growth. Using a diffusion-controlled growth law, we find that spherulites can grow on the order of days to months at temperatures above the glass transition. The diffusion-controlled growth law also accounts for spherulite size distribution, spherulite growth below the glass transition, and why spherulitic glasses are not completely devitrified. An erratum to this article can be found at     

Single-crystal polarized FTIR spectroscopy and neutron diffraction refinement of cancrinite

We relate a single-crystal FTIR (Fourier transform infrared) and neutron diffraction study of two natural cancrinites. The structural refinements show that the oxygen site of the H₂O molecule lies off the triad axis. The water molecule is almost symmetric and slightly tilted from the (0001) plane. It is involved in bifurcated hydrogen bridges, with Ow···O donor–acceptor distances >2.7 Å. The FTIR spectra show two main absorptions. The first at 3,602 cm^?1 is polarized for E ⊥ c and is assigned to the ν₃ mode. The second, at 3,531 cm^?1, is also polarized for E ⊥ c and is assigned to ν₁ mode. A weak component at 4,108 cm^?1 could possibly indicate the presence of additional OH groups in the structure of cancrinite. Several overlapping bands in the 1,300–1,500 cm^?1 range are strongly polarized for E ⊥ c, and are assigned to the vibrations of the CO₃ group.