Determination of Boron Concentration in Geochemical Reference Materials Extracted by Pyrohydrolysis and Measured by ICP‐MS

This article presents new boron concentrations for nine geochemical reference materials (GS‐N, FK‐N, GL‐O, BX‐N, DT‐N, AN‐G, GH, Mica‐Fe, Mica‐Mg). After extraction by a modified pyrohydrolysis technique, boron concentrations were measured by ICP‐MS. The blank levels for the whole procedure were 0.091 ± 0.020 ng ml^?1 or 14 ± 5 ng of boron in total. The method was first validated by measuring nine reference materials with known boron concentrations. The determined boron concentrations are all within the range of recommended or published values, which means that the yields were 100%, and show precisions below 10% for samples containing over 2 μg g^?1 of boron.     

Marine diatom Thalassirosira weissflogii nutrient drawdown and its physiological status variation challenged to zinc and cadmium exposure

The uptake of zinc and cadmium by a species of marine diatom Thalassirosira weissflogii and the nutrient variation (phosphorus and silicon) in the culture medium were estimated when exposed to zinc and cadmium stress under controlled laboratory conditions.It was found that low cadmium addition could stimulate the culture to grow with a relatively high rate and exert its toxicity at the elevated concentration.The cellular uptake of zinc and cadmium by the diatom varied in the ranges of 1.21~3.75 and 0.060~0.629 fmol per cell respectively in the whole cultivation period.The mean cellular phosphorus and silicon drawdowns were constant with 0.26~0.42 and 0.30~0.46 pmol per cell respectively in those healthy cultures.It is illustrated that the algal cells can adjust some physiological mechanisms to decrease metal accumulation and keep metal homeostasis in the organism.The correlation analysis results further indicate that the cellular cadmium uptake might be closely related with the cellular phosphorus, silicon drawdown and the growth rate of diatom (P<0.05, 0.001, 0.01); and the cultures grow better in good conditions, the lower amount of phosphorus, silicon materials are consumed by a single cell to keep a high efficiency of utilization.     

Nutrient Cycling and a Stoichiometric Model in Epidavros, a Deep Basin in the Aegean Sea

Abstract. The nutrient cycling of Epidavros, a deep basin in the Saronikos Gulf, was studied in relation to various environmental factors during 1973–1976 at a station characterized by stagnant conditions. The regeneration of nutrients was related to the consumption of oxygen, and a seasonal nutrient cycle occurred with low nutrient concentrations in the spring and summer, followed by high nutrient levels in autumn and winter. In addition high values of nitrate and silicate were observed in the deeper waters, which tended to be anoxic, although the water masses were renewed during spring 1974. The distribution pattern of nutrients together with nutrient ratios were compared with previous studies of the same and neighbouring areas as well as of other isolated basins. A stoichiometric model indicates that plankton organisms in the Epidavros basin have approximate atomic ratios for C: N: P of 150: 14:1, while the ratio of change for nitrogen and phosphorus in the water is only 8.8:1 by atoms. This is probably because of the slow rate of regeneration of nitrogenous material and/or assimilation and regeneration in organic forms. The water/plankton relation in the Epidavros basin appears to be very similar to that in the Baltic Sea.     

Colorimetric determination of nanomolar concentrations of silicate in natural waters after liquid-liquid extraction using methyl isobutyl ketone

A sensitive solvent extraction method for the determination of nonamolar concentrations of silicate in natural waters is developed. According to the traditional aqueous silicate method, silicomolybdenum blue formed by the reaction between silicate and ammoni- um molydate and reduced by metol-sulfite reagent is extracted by methyl isobutyl ketone. The absorbance can be enhanced substantially up to 10-folds. The detection limit of silicate is 8 nmol/dm^3 , which is one tenth smaller than the traditional method, with the precision of 4.0% at a silicate level of 50 nmol/dm^3 and 3.2% at a silicate level of 6 μmol/dm^3. Comparing the calibration curves in the distilled water and seawater, it can be seen that the salt effect also exists in the extraction method. However, the salt effect is a linear function of the salinity and can be corrected by simple calibration. The proposed method is successfully applied to the determination of silicate in natural waters. Natural concentrations of arsenate, arsenite and phosphate cause negligible interference.     

高平4水平井组双保钻井液技术

高平4井组水平井主要用于开发安塞长10组油藏。针对该井组上部直罗组和富县组易坍塌、下部地层钻速相对较慢、地层易造浆的特点,研究应用了环保型聚硅酸盐-黄胞胶钻井液体系。该体系具有抑制性强、润滑和剪切稀释性好的特点,有利于安全快速钻井,对环境污染极小。通过小型配浆实验确定钻井液施工方案,中测后稀释钻井液,降低钻井液滤失量和密度,加强固相控制,使用保护油层的酸溶性暂堵剂和降滤失剂,可最大限度地保护油层。     

Determination of Carbon,Hydrogen, Nitrogen and Sulfur in Geological Materials Using Elemental Analysers

This article describes a series of methods developed for the determination of total carbon (C_Total), organic carbon (C_org), hydrogen, nitrogen and sulfur. The following elemental analysers were used: LECO model RC‐412 for the determination of organic carbon, total carbon and hydrogen; LECO model CS‐200 for the determination of total carbon and sulfur; LECO model TN‐400 for the determination of nitrogen; and LECO model TruSpec CHNS for the determination of organic carbon, total carbon, hydrogen, nitrogen and sulfur. Uncertainty and limits of detection and quantification were calculated for each method, as well as the running costs to define the most effective instrument for each material and each analyte. Accuracy was checked by the application of the Sutarno–Steger test. Finally, a compilation of the results obtained in the determination of C_Total, C_org, H, N and S in forty‐nine reference materials is presented.     

硅酸钡铜的光吸收谱和EPR谱

本文报道水热合成硅酸钡铜(BaCuSi_4O_(10))的光吸收谱和EPR谱。EPR测量表明,在硅酸钡铜中,Cu~(2 )离子位置有轴对称性。在这种对称性下,一般只能观察到三条Cu~(2 )离子的吸收谱带,但在BaCuSi_4O_(10)的吸收谱中却观察到了四条。这一矛盾用~2Eg激发态的动态Jahn-Teller效应来解释。本文提出的~2Eg和~2A_1g能级的相对次序与文献[2]的相反,文中对这一问题作了详细的分析。跃迁频率和g因子的计算值在实验误差范围内与观测值一致。     

Geochemical processes controlling silica concentrations in groundwaters of the Salado River drainage basin, Argentina

Chemical analyses of dissolved silica in the shallow groundwater of the lower part of the Salado River drainage basin indicate that silica values averaged 60 ppm. The groundwaters are oversaturated in relation to quartz, Na-plagioclase, K-feldspar, and the weathering of quartz and aluminosilicates appear to have little control on silica concentrations in solution. Groundwater is undersaturated with respect to amorphous silica present in the loessic sediments, and these sediments are specially important in the control of the groundwater composition. The sources of amorphous silica are volcanic glass shards and biogenic silica derived from plant (silicophytoliths, diatom frustules) or animal remains (sponge spicules) also present in the Pampean loess. Silicophytoliths and diatoms have also been reported in A soil horizon samples. The dissolution of amorphous silica most likely controls the high dissolved silica concentrations in groundwater.     

我国发现的钇硅磷灰石

我国首次发现的钇硅磷灰石产于河南含稀有金属的花岗岩内,为磷灰石型结构的硅酸盐矿物。乳白、玫瑰、棕色,实测比重4.35,一轴负晶,ω=1.784,ε=1.991。探针分析计算化学式为:(Y_(3.17)Ca_(1.56)Dy_(0.22)…)[(Si_(0.92)P_(0.03))O_4]_3(OH,F),P6_3/m,α=9.426±0.008,c=6.806±0.007。还进行了X射线粉晶衍射分析和红外吸收光谱分析,最后对具磷灰石型结构矿物种间阳离子、阴离子、附加阴离子之间的置换方式进行了讨论。     

Comparison of Two Sample Preparation Methods for X‐Ray Fluorescence Spectrometry in the Determination of Ni and Cr

Pressed powder pellets and fused beads or glass disks are routinely used in X‐ray fluorescence spectrometry for the determination of major and trace elements, respectively, in geological materials. In order to evaluate the performance of these two sample preparation methods, we determined Ni and Cr concentrations of fourteen RMs from Japan, France and South Africa, and eighty‐five igneous and three sedimentary rock samples from Mexico in both powder pellets and glass beads. We also computed new values of statistical parameters for RMs from an outlier‐based multiple‐test method and compared them with the literature mean and confidence limit values. The results showed that the multiple‐test method provided more reliable central tendency and dispersion parameters for RMs than those obtained previously from the two or three standard deviation method, or from robust methods. The powder pellet and fused bead sample preparation methods provided consistent results for Ni and Cr at concentration levels > 50 μg g^?1 in this application; for lower concentration levels, however, these methods showed somewhat greater differences. For quantitative comparisons, both ordinary and weighted least‐squares linear regression models were used to show that the two sample preparation methods provided generally unbiased results.