珠江口表层水中主要常量离子的研究

９９４年９月采集了珠江口表层海水水样,并对其溶解态的Ｋ＋、Ｎａ＋、Ｃａ２＋、Ｍｇ２＋、ＳＯ２－４、Ｃｌ等化学要素进行了测定。结果表明,珠江口调查海域表层水中溶解态的Ｋ＋、Ｎａ＋、Ｃａ２＋、Ｍｇ２＋、ＳＯ２－４主要受陆源淡水与外海水物理混合稀释的影响,与Ｃｌ具有良好的直线正相关;Ｃａ２＋／Ｃｌ、ＳＯ２－４／Ｃｌ明显高于大洋水相应比值,Ｎａ＋／Ｃｌ、Ｍｇ２＋／Ｃｌ略高,而Ｋ＋／Ｃｌ比大洋比值低;在与中国其它各主要河口表层水对应Ｃｌ比较中,珠江口的ＳＯ２－４／Ｃｌ较高,而Ｃａ２＋／Ｃｌ,Ｍｇ２＋／Ｃｌ比值居低;上述各主要常量离子和Ｃｌ的等值线均沿自北向南走向递增。     

有孔虫壳体的Mg/Ca比值在古环境研究中的应用

有孔虫壳体的Mg/Ca比值测定是目前估算海水古温度最受重视的方法,适用于低纬和高纬、表层和深层海水古温度的测定。该方法理论误差仅为±1.1℃,考虑到盐度以及海水pH值的影响,其误差为±1.3℃。运用此法推算出的热带海区表层海水温度领先于全球冰盖的变化,是热带过程调控冰期旋回最强有力的证据之一;与氧同位素相结合,还成功地运用于全球冰量的估算,是目前古环境研究中较常用的古温度测试手段。     

吐哈盆地北缘中侏罗世植物化石稳定碳同位素的古环境意义

新疆吐哈盆地北缘三道岭煤田中侏罗统西山窑组的植物化石属于Coniopteris-Phoenicopsis植物群的典型组合。从该植物群中挑选出优势属种,分别为似银杏、拟刺葵、枝脉蕨以及斯堪尼狭轴穗,对其进行稳定碳同位素分析。前3种为叶片化石,它们的δ13C值分布在-21.66‰~-23.83‰,属于典型的C3植物。最后一种为繁殖器官化石,其δ13C值为-20.91‰,比叶片的值高。将δ13C值根据公式转换为大气CO₂的δ13C_a值,发现基于银杏类叶片获得的现代和中侏罗世的δ13C_a值与其他方法获得的值相似。这说明银杏类叶片是重建地质历史时期δ13C_a的一类可靠植物,为今后研究中生代-新生代δ13C_a变化提供了一个简便而可行的方法。C_i/C_a比值是一重要的植物生理生态特征值,因此进一步将银杏类化石叶片的δ13C值换算成C_i/C_a。化石似银杏的C_i/C_a值为0.6,而现生银杏的C_i/C_a为0.63,二者相似。虽然三道岭地区中侏罗世的CO₂浓度约为现在的4.5倍,但是化石和现生银杏类植物的C_i/C_a值仍然保持恒定,表明银杏植物的气孔参数对CO₂变化比较敏感,是重建古CO₂浓度的良好指示植物。这也为判断一种植物能否用来重建古CO₂浓度提供了一种简便而有效的检测方法。     

青藏高原湖泊Mg~(2+)、Ca~(2+)和Mg/Ca盐度指示意义的初步分析

总结了青藏高原地区400多个湖泊湖水的Mg2+、Ca2+和Mg/Ca等水化指标与湖水盐度的相关关系,以及这种关系随着湖水变化(不同采样时间和采样点以及自然蒸发)而产生的变化规律.结果表明:青藏高原湖泊湖水的Mg2+浓度与盐度具有较为稳定的正相关关系,而Ca2+和Mg/Ca与盐度的相关性较弱.在对于某一特定水化学类型的湖泊,一般碳酸盐型湖泊的Mg2+、Ca2+以及Mg/Ca等指标与盐度均没有明显的相关性;硫酸盐型湖泊中Mg2+浓度和盐度呈现较高的正相关关系,而Ca2+以及Mg/Ca与盐度的相关性仍很弱;而在氯化物型湖泊中,Mg2+浓度与盐度呈更高的正相关性,Ca2+浓度也与盐度呈一定的正相关性,Mg/Ca这一指标与盐度的相关性依然很弱.而对某一特定湖泊,在不同演化阶段或不同的采样地点,Mg2+浓度与盐度仍然保持明显的正相关关系,而Ca2+以及Mg/Ca与盐度的相关性仍然不稳定或很弱.在青藏高原作古环境重建应用的时候,湖水Mg2+浓度是古盐度一个较好的转换指标,而Ca2+以及Mg/Ca的古盐度指示意义相对较弱.     

Treatment of Arsenic Contaminated Groundwater Using Calcium Impregnated Granular Activated Carbon in a Batch Reactor: Optimization of Process Parameters

This paper is an experimental investigation into the removal of arsenic species from simulated groundwater by adsorption onto Ca²⁺ impregnated granular activated carbon (GAC‐Ca) in the presence of impurities like Fe and Mn. The effects of adsorbent concentration, pH and temperature on the percentage removal of total arsenic (As(T)), As(III) and As(V) have been discussed. Under the experimental conditions, the optimum adsorbent concentration of GAC‐Ca was found to be 8 g/L with an agitation time of 24 h, which reduced As(T) concentration from 188 to 10 μg/L. Maximum removal of As(V) and As(III) was observed in a pH range of 7–11 and 9–11, respectively. Removal of all the above arsenic species decreased slightly with increasing temperature. The presence of Fe and Mn increased the adsorption of arsenic species. Under the experimental conditions at 30°C, the maximum percentage removals of As(T), As(III), As(V), Fe, and Mn were found to be ca. 94.3, 90.6, 98.0, 100 and 63%, respectively. It was also observed that amongst the various regenerating liquids used, a 5 N H₂SO₄ solution exhibited maximum regeneration (ca. 91%) of the spent GAC‐Ca.     

含钙铝铁水解聚合产物的矿物学研究Ⅱ:热分解特性

分别以NaOH和Ca(OH)2作为碱化剂,合成了聚合氯化铝铁(PAFCNa,PAFCCa),比较样聚合氯化铝(PACNa,PACCa)、聚合氯化铁(PFCNa,PFCCa),制成低温干燥样进行热分解检测.热重分析证明,PAFCCa中的含水量高,主要是配位水与结晶水.当n(Al)/n(Fe)>5:5后,PAFCCa的含水量平均为42.3%.按Ca6Al2(SO4)3(OH)12·26H2O分子式计算,钙矾石的结构水(含OH水)含量为43.06%,两者含水量相当接近.TG-DTG热分析结果支持XRD对PAFCCa中存在含Ca3Al2(OH)12柱体的类钙矾石结构体的认定.PAFC-Ca根据其DTG曲线上的125℃和180℃两个脱水速率(肩)峰可以判别其中有无钙矾石结构体,以及相对量的多少.     

黄旗海湖泊沉积记录的早中全新世大湖期环境的差异性

内蒙古黄旗海H6剖面揭示了最近间冰期古湖泊涨缩的一个完整旋回。基于OSL年代、粒度并结合沉积物地球化学等数据,分析了黄旗海在早、中全新世（约（11.4±1.1～6.7±0.7）ka）大湖期指标记录特点与环境意义。研究认为黄旗海全新世大湖期可分为三个阶段:1）（11.4±1.1～9.3±0.9） ka BP,半深水环境、湖水盐度低、流域存在有利于化学风化的湿润气候条件;2）（9.3±0.9～7.7±0.7） ka BP,湖水变浅、湖泊萎缩、湖泊盐度升高,流域可能存在不利于化学风化的干燥气候;3）（7.7±0.7～6.7±0.7） ka BP,大湖期结束,指标记录存在剧烈波动,揭示气候具有宽幅震荡特征。同时,研究初步认为Mn/Li比值可以作为流域化学风化的指标指示。     

The Rumuruti chondrite group

Since 1994, the Rumuruti (R) chondrites have been recognized as a new, well-established chondrite group differing from carbonaceous, ordinary, and enstatite chondrites. The first R chondrite, Carlisle Lakes, was found in Australia in 1977. Meanwhile, the number has increased to 107 (December, 2010). This group is named after the Rumuruti meteorite, the first and so far the only R chondrite fall. Most of the R chondrites are breccias containing a variety of different clasts embedded in a clastic matrix. Some textural and mineralogical characteristics can be summarized as follows: (a) the chondrule abundance in large fragments and in unbrecciated rocks is ∼35–50 vol%; (b) Ca,Al-rich inclusions are rare; (c) the olivine abundance is typically 65–78 vol%; (d) the mean chondrule diameter is ∼400 μm; (e) in unequilibrated R chondrites, low-Ca pyroxene is dominating, whereas in equilibrated R chondrites it is Ca-rich pyroxene; (f) the typical olivine in a metamorphosed lithology is ∼Fa_38–40; (g) matrix olivine in unequilibrated, type 3 fragments and rocks has much higher Fa (∼45–60 mol%) compared to matrix olivines in type 4–6 lithologies (∼Fa_38–41); (h) spinels have a high TiO₂ of ∼5 wt%; (i) abundant different noble metal-bearing phases (metals, sulfides, tellurides, arsenides) occur. The exception is the metamorphosed, type 5/6 R chondrite La Paz Icefield 04840 which contains hornblende, phlogopite, and Ca-poor pyroxene, the latter phase typically occurring in low-grade metamorphosed R chondrites only.In bulk composition, R chondrites have some affinity to ordinary chondrites: (a) the absence of significant depletions in Mn and Na in R chondrites and ordinary chondrites is an important feature to distinguish these groups from carbonaceous chondrites; (b) total Fe (∼24 wt%) of R chondrites is between those of H and L chondrites (27.1 and 21.6 wt%, respectively); (c) the average CI/Mg-normalized lithophile element abundances are ∼0.95 × CI, which is lower than those for carbonaceous chondrites (≥1.0 × CI) and slightly higher than those for ordinary chondrites (∼0.9 × CI); (d) trace element concentrations such as Zn (∼150 ppm) and Se (∼15 ppm) are much higher than in ordinary chondrites; (e) the whole rock Δ¹⁷O of ∼2.7 for R chondrites is the highest among all meteorite groups, and the mean oxygen isotope composition is δ¹⁷O = 5.36 ± 0.43, δ¹⁸O = 5.07 ± 0.86, Δ¹⁷O = +2.72 ± 0.31; (f) noble gas cosmic ray exposure ages of R chondrites range between ∼0.1 and ∼70 Ma. More than half of the R chondrites analyzed for noble gases contain implanted solar wind and, thus, are regolith breccias. The 43 R chondrites from Northern Africa analyzed so far for noble gases seem to represent at least 16 falls. Although the data base is still scarce, the data hint at a major collision event on the R chondrite parent body between 15 and 25 Ma ago.     

习水县岩溶水系统ρ(Sr2+)、ρ(Sr)/ρ(Ca)、ρ(Sr)/ρ(Mg)分布特征及其应用

通过对流域内不同类型水取样分析,发现流经不同岩层的地下水具有不同的ρ(Sr2+)、ρ(Sr)/ρ(Ca)、ρ(Sr)/ρ(Mg)值.一般来说,流经砂岩层的基岩裂隙水ρ(Sr2+)低,而ρ(Sr)/ρ(Ca)、ρ(Sr)/ρ(Mg)值较高,当砂岩中的基岩裂隙水受到灰岩岩溶水或煤系地层水补给时,其ρ(Sr2+)、ρ( Sr...     

激光剥蚀电感耦合等离子体质谱分析石笋样品中多元素比值及45种元素含量

石笋样品的微量元素含量及Mg/Ca、Sr/Ca比值为高分辨的古气候重建提供重要指标。针对现有溶液分析技术易混合多个石笋微层、误差大的缺点,本文利用激光剥蚀电感耦合等离子体质谱技术(LA-ICP-MS)原位线扫描和点剥蚀方式对比分析了石笋生长轴方向的Mg/Ca和Sr/Ca空间分布趋势,研究表明二者均展现出显著的周期性变化特征,且周期性变化一致,其中40 μm束斑线扫描更具有稳定性强、分辨率高、快速简便的优点。通过探讨碳酸盐标准样品MASC-3与玻璃标准样品NIST 610、NIST 612、KL2G、ATHO-G的相对灵敏度系数关系和元素分馏行为,确定基体效应是造成相对灵敏度系数变化的主要原因。同时建立了以MASC-3、NIST 610和NIST 612多外标结合内标Ca归一定量分析石笋中45种元素方法,针对石笋碳酸盐样品,将主量元素Ca、Mg变形为碳酸盐形式,与其他元素加和归一,不仅改变了国内外研究中需要预先采用其他分析技术来测定内标元素含量的计算方法,而且有效地避免了C元素无法准确检测的问题,能够实现与Ca内标法校正结果的吻合。