海水中镉（Ⅱ）与水合氧化钛无机离子交换反应的研究

海洋化学研究的一个主要内容是海水中元素的迁移和变化规律的探索。已经发现，这是与海水中的水合氧化物、粘土矿物和若干有机物之间的离子交换作用密切相关的。在本文中无机离子交换剂是水合氧化钛，金属元素为镉，作为这一方面系统研究工作(在这系列工作中，     

THE INTERACTION OF COPPER WITH GOETHITE, HEMATITE AND AMORPHOROUS IRON OXIDE IN SEAWATER

1.This paper deals with a discovery of ours-a new type of isotherm in seawater systems, which cannot be represented by the adsorption isotherm equation available at present in marine chemistry. It has two characteristics as follows: (I) the non-linear relationship between the ion exchanged amount of particulate matter and the equilibrium concentration in the initial low concentration portion of the curve, showing instead an exponental function with slight concave upward. (2) the isotherm is made up of two “S shape” curves, which intersect each othernear the middle, with one “Knee” and two“Plateaus” at the intersection.     

从海水中提取铀的发展现状

综述了几种常见海水中提取的方法和途径，并对其进行了分析和比较，对于具有开发价值的新方法和新作途径进行了较详细的讨论，对重要的吸附剂如肟胺类吸附剂的合成，优化等作为较详细的介绍，通过本文可以为从事该类工作的科技人员提供一个较全面的参考。     

Speciation of adsorbed arsenate on the surface of hydrous iron oxide

Adsorption of arsenate on hydrous iron oxide is an important process controlling geochemical cycling of arsenic in environment as well as the fate of arsenic-bearing mining wastes. The widely accepted view on the mechanism of adsorption is that arsenate is adsorbed via bidentate binuclear inner-sphere complexation. In this study, we characterized the arsenate-hydrous iron oxide sorption solids synthesized at pH=3-8 using Fourier transformed infrared spectroscopy （FTIR） and X-ray diffraction （XRD）. It has been determined that poorly crystalline ferric arsenate developed on the surface of iron oxide when arsenate was sorbed at acidic pH, while at alkaline pH the adsorption of arsenate was via bidentate complexation.     

细菌浸铜技术在紫金山铜矿的应用

介绍了生物浸矿技术在紫金山铜矿的应用及在这一过程中发现的一些问题，并提出了有待进一步解决的一些问题。     

西昆仑山南侧甜水海湖岩芯铁变化的环境记录

阐述了青藏高原西昆仑山南侧甜水海湖岩芯沉积物中氧化铁的丰度、频率分布和富集系数的变化规律。其丰度值范围FeO0．39％-3.95％，平均值为1．25％；Fe2O30．44％－8．09％，平均值为2．60％；Fe2O3／FeO0．21－3．60，平均比值1．12。说明该彻岩芯沉积物中铁平均丰度值较低，但其变化幅度较宽且清楚，在一定程度上反映了古气候环境具有较大幅度的波动。变异系数值表明，该湖岩芯沉积物中FeO的离散程度较Fe2O3大。大约距今23万年来氧化铁的沉积地球化学特征可划分出7个环境演化阶段，并基本上可与深海氧同位索阶段对比。揭示了甜水海湖演化与青藏高原强烈隆升引起的气候环境改变的密切关系。在距今23一15万年，沉积以河流相或冲积、洪积相为主，沉积环境以氧化环境为主导，气候以温干型波动；在距今15－7．4万年，沉积以湖相为主，沉积环境以还原环境为主导，气候以温湿型为主；在距今74万年以来，湖盆沉积环境多样化，沉积物以湖相和近源冲积、洪积相交替出现。气候出现冷湿、冷干、温湿和温干多种波动模式。这些资料分析初步认为甜水海古湖大约形成于距今15万年，即青藏高原第三成湖期，这也与青藏高原在距今15万年左右的再次构造隆升有关。     

Rb2Ca[B4O5(OH)4]2·8H2O溶解及相转化过程的研究

利用IR光谱和Raman光谱等实验手段,对25℃时Rb2Ca[B4O5(OH)4]2·8H2O的溶解及相转化过程进行了初步探索,结果表明,Rb2Ca[B4O5(OH)4]2·8H2O溶于水后,硼在溶液中主要以B(OH)3和[B(OH)4]-的形式存在,残留固相由开始的无定形水合三硼酸钙,最终部分转变为Ca2[B3O3(OH)5]2·8H2O晶体。     

浓硫酸钠水溶液中的离子对

不同浓度的Na2SO4水溶液的拉曼光谱显示了SO42-的四个拉曼活性带:980 cm-1处的SO42-的对称伸缩振动模式v1带,1 106 cm-1处的反对称伸缩振动模式v3带,448 cm-1处的变形振动模式v2带和617 cm-1处的变形振动模式v4带。482 cm-1处的肩膀峰是由于NaSO4-离子对的形成对448 cm-1的v2带的影响而形成的SO42-的一个新的振动峰。浓Na2SO4水溶液中,水共享离子对[Na+.H2O.SO42-]-是主要的离子对物种。随着Na2SO4水溶液浓度的增加,Na+和SO42-的相互作用增强,NaSO4-离子对所占的摩尔分数增加。     

DFT对Rb+水合团簇及其相关性质的分析

运用密度泛函理论(DFT)在ωB97XD/gen (O、H元素Aug-cc-PVDZ; Rb元素Lanl2DZ)基组水平上研究了[Rb(H_2O)_n]~+(n=1～12)水合团簇的结构和光谱学性质。研究结果表明,通过分析气相和液相中的稳定能以及水合团簇可知,稳定构型出现在8配位的团簇中。第一配位层水分子数为8时形成Rb~+第一近似饱和水合层。此外,拉曼光谱显示[Rb(H_2O)_n]~+(n=1～12)水合团簇中O-H伸缩振动峰随着水分子数增加发生移动和加宽,Rb~+发生水合时,O-H对称和非对称伸缩振动发生红移,随着水合数的增多,频率蓝移。此外,文中对拉曼光谱中O-H振动的频率位置结合团簇结构进行了说明。     

Report of Prionospio complex (Annelida: Polychaeta: Spionidae) from China's waters, with description of a new species

Nine species of Prionospio complex are recorded from China’s waters, including one new species and six newly recorded species. Prionospio (Prionospio) pacifica sp. nov., is characterized by having first and forth pairs of branchiae pinnate, second and third pairs of apinnate, ventral crest on Setiger 9 and dorsal crests on Setigers 10—25. Apoprionospio kirrae (Wilson, 1990), Prionospio (Aquilaspio) convexa Imajima, 1990, Prionospio (Minuspio) multibranchiata Berkeley, 1927, Prionospio (Prionospio) bocki Sderstrm, 1920, Prionospio (Prionospio) dubia Maciolek, 1985 and Prionospio (Prionospio) paradisea Imajima, 1990 are recorded for the first time from China’s waters.