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1.
This article reports a preliminary research on silicate-incorporated hydroxyapatite as a new environmental mineral used to remove cadmium ions from aqueous solutions. The silicate-incorporated hydroxyapatite was prepared by coprecipitation and calcining, and silicate was incorporated into the crystal lattice of hydroxyapatite by partial substitution of phosphate. The amount of cadmium ions removed by silicate-incorporated hydroxyapatite was significantly elevated, which was 76% higher than that of pure hydroxyapatite. But the sorption behavior of cadmium ions on silicate-incorporated hydroxyapatite was similar to that of pure hydroxyapatite. Morphological study revealed that silicate incorporation confined the crystal growth and increased the specific surface area of hydroxyapatite, which were in favor of enhancing the cadmium ion sorption capacity of the samples. Incorporation of silicate into hydroxyapatite seems to be an effective approach to improve the environmental property of hydroxyapatite on removal of aqueous cadmium ions.  相似文献   

2.
Solid phases, such as surface coatings （SC）, suspended particulate matter （SPM） and deposited sediments （DS）, contribute to the pool of heavy metals in natural waters. Their existing and forming conditions lead to potential differences in enrichment capacity of pollutants, chemical compositions and crystals. In this study, the contents of heavy metals in SC, SPM and DS were determined by GF-AAS after digestion with a mixture of concentrated HNO3 and HClO4. The selective extraction method was employed to remove Fe, Mn oxides and organic matters and associated heavy metals （Cu, Pb, Zn）. X-ray diffraction analyses were performed to characterize the crystals in the samples. The results showed that no significant difference in the contents of Fe-oxides in DS, SPM and SC was found, but the contents of Mn-oxides and organic matter follow the order of SC〉SPM〉DS. The significant crystal characters were observed in DS, SPM and SC, and the kinds of minerals and crystallization degree follow the order of DS〉SC〉SPM. In addition, quartz was the most important matter of crystals in the solid phases. Enrichment capacity follows the order of SPM〉SC〉DS for Pb, Cu and Zn. Organic matter was the major sorbent for Cu, and Mn oxides and organic matter played an important role in the enrichment of Zn. However, Pb was absorbed mainly by Fe oxides. Moreover, compared with Fe oxides and organic matter, Mn oxides had a great enrichment capacity for these metals. Although DS, SPM and SC were formed in the same water system, contents of chemical components, crystals and enrichment capacities to heavy metals were obviously different.  相似文献   

3.
Isotopic compositions of the water sources and evapotranspiration in large rivers of China are not well explored. In this investigation, d18 O and dD values of water from major large rivers of China are integrated to understand the spatial and temporal variations in the isotopes of water and d-excess. River water samples were collected from the channels and tributaries of the Changjiang, Yellow, Songhua and Liao Rivers in China. Water from upstream was generally enriched with light isotopes relative to that from downstream areas. Water from the Songhua River and upper reach of the Changjiang River has relatively negative isotopic values impacted by latitude and altitude effects, respectively. The spatial pattern showed that d18O-H2 O values in rivers mainly ranged from-9 to-7 % in most of China based on roughly mapped contours, and rivers enriched in light isotopes were primarily located in the Tibetan Plateau and northeast China The slopes of linear regression from the Yellow and Liao Rivers suggested that the loss of water by direct evaporation shifted the isotopes of water, especially in some small tributaries. Additionally, there was a narrow range of low d18OH2 O values from the main channel of rivers during the lowflow season relative to the high-flow season due to influence of the monsoon climate. No distinct spatial variation of d-excess values was found in the rivers of China. However, water samples in some rivers with low d-excess values had high d18 O values, indicating that evaporation in the tributaries has led to significant water loss, especially in tributaries of the Yellow and Liao Rivers.  相似文献   

4.
This paper deals with a simulated test of biogenic mineralization made with a blue-green alga species,Spirulina platensix. The data in the experiment were recorded by a computerized surveying system. The influ-ence of algae on the accumulation of phosphorus by changing their microenvironment to promote the forma-tion and deposition of phosphate was studied. The results show that the pH value of cultural liquor rose up to 10 and the redox potential (Eh) may dropby 100-200 mV during the algal logarithmic growth stage, and the cultrual liquor was changed into a mediumwith a weakly reducing condition. At the end of the logarithmic growth stage white deposits of Na_2Ca(CO_3)_2·5H_2O and Ca_2Mg (PO_4)_2·2H_2O were formed on the floor of cultural containers. The test presented a wduableevidence for the theory of biogenic mineralization.  相似文献   

5.
The Sepetiba Bay is a shallow water body semi enclosed located on the west side of Rio de Janeiro City. Almost 80% of flesh water discharge, from the St Francisco canal, coming from the northern side of the bay develops an estuarine environment. Fishing and tourism are some of the most important economic activities in the area. During 35 years a zinc/cadmium smelter has polluted the bay. The objective of this investigation is to demonstrate the diagenetic processes and cadmium remobilization into pore water from the contaminated sediments. Two sites were selected to compare diagenetic processes. Site P1 is located next to domestic effluents discharge into the bay and approximately 20km away from the smelter. Site P2 is located near the same smelter and next to the Mazomba estuary, which is not influenced directly by domestic effluents. Peeper samplers of 25 cells with a resolution of 2.5 cm were deployed at both the sites. After a 3-weeks period of equilibrium, the pore waters were separated from the cells and analyzed immediately （within 24 h） for alkalinity, NH3 and reactive soluble phosphorus on a spectrophotometer. An ICP-AESΣH2S spectrometer was used to analyze Na, Mg, Li, Ba, Sr, Si, Fe and Mn. Total and labile dissolved Cd in pore waters were determined by differential-pulse stripping voltametry. The dissolved constituents in the pore waters have shown that the intensities of diagenetic reactions are different between sites. The reactions are stronger at site P1 site than at site P2, especially between 7.5 cm and 22.5 cm, which is evident by the organic rich sediment.  相似文献   

6.
The Mengyejing potash deposit is located in the southern port of the Simao Basin, Yunnan Province, and is hosted in mid-Cretaceous strata. The chemical compositions of fluid inclusions in halite crystals, collected from the level-610 adit in the deposit, were analysed by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The results show that the brine is of the Na-K-Mg-Ca-Cl type and has K concentrations that are distinctly higher than those of Mg and Ca, unlike normal brines associated with Cretaceous halite. The high K concentrations indicate that the degree of evaporation of the ancient Mengyejing saline lake was very high, reaching the sylvite deposition stage but rarely reaching the carnallite deposition stage. The trajectory of the H and O isotopic compositions of the brines in the halite-hosted fluid inclusions corresponds to intense evaporation, indicating that the net evaporation exceeded the net inflow of brines. These brine compositions in halite-hosted fluid inclusions were likely formed by the dissolution of previously deposited K-bearing minerals by fresh continental and/or seawater, forming a type of modified seawater, with deep hydrothermal fluids potentially supplying additional potassium. The basin likely experienced multiple seawater incursion, dissolution and redeposition events in a high-temperature environment with high evaporation rates.  相似文献   

7.
The Khorat Plateau on the Indochina Terrane is known to have formed during the closure of the Tethys Ocean, although the origin of its potash mineral deposits is a topic of current debate. Data from a borehole on Savannakhet Basin is used in this study to re-define the evaporation processes of the study area. Geochemical analyses of halite from various borehole-derived evaporite strata have elucidated the fluid sources from which these ores formed. Measured δ11 B indicated that ore deposits formed primarily due to evaporation of seawater, although non-marine fluids affected the later stages of the evaporation process. Fluctuations in B and Br concentrations in carnallite-and sylvite-rich strata indicate the influence of fresh water. Boron concentration in carnallite unit indicated the influence of hydrothermal fluids. From the relative timings of these various fluid influxes, the evolution of these evaporates can be divided into four stages:(1) an initial marine evaporation at the beginning of the deposit's formation, where seawater(and minor fresh water) trapped on the uplifted Khorat Plateau produced sediments and salts with Br contents lower than those of normal marine-derived evaporites;(2) a transgression stage, where seawater recharged the basin;(3) a hydrothermal infiltration stage, which was coeval with the late Yanshan movement; and(4) a stage of fresh water supply, as recorded by fluctuations in B and Br contents, inferring intermittent fresh water influx into the basin. Thus, although evaporites on the Savannakhet Basin primarily formed via marine evaporation, they were also influenced to a significant degree by the addition of non–marine fresh water and hydrothermal fluids.  相似文献   

8.
CO2 dissolution into an aqueous phase and water evaporation into a gaseous phase takes place during CO2 injection into an oil reservoir. This study aims to evaluate the phase behaviors of the oil-gas-water system in the displacement of crude oil by CO2. The composition of the JL oilfield in the northeast of China is taken as an example. The flash calculation of the oil-gas-water system was performed, based on the method presented by Li and Nghiem. The research re...  相似文献   

9.
Experiments have been performed on the system MgO-SiO2-Cr-O at 0-2.88 GPa and 1100-1450℃,focusing on the stability of Cr^2 in olivine(O1),orthopyroxene(Opx) and spinel(Sp) and its partitioning between these phases.Analytical reagent grade chemicals,MgO,SiO2,Cr2O3.and Cr were used to make starting mixtures.Excess Cr(50%) was then added in these mixtures to ensure that the resultant phases were in equilibrium with the metal Cr.Flux of BaO B2O3(%) was added for facilitating experimental equilibrium and crystal growth.Cr was used as capsule material.All phases in the product were identified by X-ray and analyzed by electron microprobe,The contents of CrO in the different phases(O1,Opx and Sp)were calculated according to stoichiometry.The obtained results of calculation indicate that Cr^3 in Ol and Opx is negligible.The experimental results show;(a) with increasing temperature and decreasing pressure,Cr^2 solubility in Ol,Opx and Sp increases;(b) with in creasing temperature,the partitioning coefficient of Mg and Cr^2 between Ol and Opx decreases,that between Opx and Sp increases,and that between Ol and Sp remains almost unchanged;(c) the effect of pressure on all partitioning coefficients is negligible.  相似文献   

10.
Livestock wastes applied to agricultural land are potential sources of steroidal hormones （estradiol （E2）, estrone （E1）, and estriol （E3）） that can adversely affect the aquatic ecosystem as endocrine disruptors. But the effects of plants on the fate of estrogen in the environment are not clearly known. In the present report, the behavior of E1, E2 and E3 added to the rhizospheric soil in various concentrations and its effect on plant growth were examined by estrogen batch sorption test, plant pot test and estrogen extraction test. Trifolium repens was grown on the soil spiked with E2 or a mixture of E1, E2 and E3. Pots without plant were prepared as controls. All pots were watered in 50 ml dose almost every day, and the rhizosheric soil and plant body were collected 7, 19, 26, 33 days after planting. The soil was sequentially extracted with Milli-Q water, and methanol / 1M acetic acid solvent followed by methanol wash at the solid to liquid ratio of 1 ： 4 （g/mL）. Extracts were analyzed for El, E2 and E3 using a Shimadzu GCMS-QP5050. Plant dry weight （4 hours, 105 ℃） was measured as an indicator of plant growth. In batch sorption tests, E1 and E2 concentrations in the liquid phase significantly decreased within 24 hours after the addition of estrogen. The sum of methanol / 1M acetic acid extractable E 1 and E2 in the soil decreased to half of the initial added amount within 7 days. Reduction in total estrogenic activity of the soil extracts （estimated as 0.01CE1＋CE2＋0.1CE3 where CE1, CE2 and CE3 are respective El, E2 and E3 concentrations per unit soil weight） continued for 1 month due to slow oxidation of E2 to E1. Desorption of E2 from soil during the pot experiment was higher than expected from the sorption experiment.  相似文献   

11.
Single crystals of emerald synthesized by means of the flux method were adopted for crystallographic analyses. Emerald crystals with a wide range of Cr3+-doping content up to 3.16 wt% Cr2O3 were examined by X-ray single crystal diffraction refinement method. The crystal structures of the emerald crystals were refined to R 1 (all data) of 0.019–0.024 and wR 2 (all data) of 0.061–0.073. When Cr3+ substitutes for Al3+, the main adjustment takes place in the Al-octahedron and Be-tetrahedron. The effect of substitution of Cr3+ for Al3+ in the beryl structure results in progressively lengthening of the Al–O distance, while the length of the other bonds remains nearly unchanged. The substitution of Cr3+ for Al3+ may have caused the expansion of a axis, while keeping the c axis unchanged in the emerald lattice. As a consequence, the Al–O–Si and Al–O–Be bonding angles are found to decrease, while the angle of Si–O–Be increases as the Al–O distance increases during the Cr replacement.  相似文献   

12.
俄罗斯富铁型水热法合成祖母绿特征研究   总被引：1，自引：0，他引：1  
针对近期市场上出现的俄罗斯富铁型水热法合成祖母绿,采用电子探针、傅里叶变换红外光谱仪和紫外-可见光谱仪等测试分析方法,从化学成分、宝石学特征及谱学进行初步研究。结果表明,俄罗斯富铁型水热法合成祖母绿内部有特征的红棕色假六方片状金属固体包裹体,化学成分以贫碱富铁含铜为特征,环状分子通道内I型水和Ⅱ型水同时存在,在760nm处有由Fe3＋的d-d电子跃迁导致的特征吸收峰。除此之外,笔者对比分析了俄罗斯富铁型、传统水热法合成祖母绿、桂林水热法合成祖母绿、助熔剂法合成祖母绿及天然祖母绿样品在谱学上的差异。  相似文献   

13.
云南祖母绿的矿床地质及宝石学特征   总被引：4，自引：0，他引：4  
张良钜  兰延 《矿物学报》1999,19(2):189-197
云南祖母绿矿床产于寒武系变质岩中,矿体分别产于片麻岩的伟晶岩及云英岩脉中。属于典型的伟晶岩型或气成高温热液矿床。祖母绿的铬、钒来源于变质岩,而铍来源于伟晶岩。  相似文献   

14.
板状绿柱石晶体的结构测定   总被引：12，自引：0，他引：12  
郭延军 Fontan  F 《地质论评》2000,46(3):312-317
自然界中绿柱石晶体多为柱状,具板状晶形的绿柱石非常少见。本文对产于四川雪宝顶云英岩晶洞中的无色透明板状绿柱石进行了精确的结构分析,并与产于阿尔泰山号伟晶岩脉中的柱状绿柱石进行了比较。与阿尔泰柱状绿柱石相比,雪面板状绿石富Ｌi、Ｎａ,ｃ／ａ值较高,为１．００１,属钠－锂绿柱石或“四面体”绿柱石。本文还对这种特殊形貌柱石的形成机制进行了初步讨论,成矿流体中Ｌi的浓度以及Ｓi的化学形态可能是影响柱石忻驳闹  相似文献   

15.
采用显微镜和XRD,EMPA,FTIR,RAMAN,TGA等现代测试方法对内蒙赤峰鱼眼石的晶体形态、矿物组合、化学成分、谱学特征、热力学性质等进行了测试分析,初步探讨了鱼眼石晶体形态的成因以及水的赋存状态。赤峰鱼眼石晶体呈粒状—假立方状,由四方柱{100}、四方双锥{111}和平行双面{001}聚合而成,无色-浅粉红色,玻璃光泽,透明到半透明,与钙铁辉石、雪硅钙石和毒砂等矿物共生。赤峰鱼眼石的主要化学成分为w(SiO_2)50.22%~52.73%,w(CaO)24.16%~25.28%,w(K_2O)3.57%~5.80%和w(F)2.62%~3.48%,含有少量的Na_2O,Al_2O_3和Cr_2O_3,平均成分的晶体化学式为:(K0.964Na0.109)1.073Ca4.036[(Si7.727Al0.091Cr0.073)7.891O20](F0.828OH0.172)1.000·7.775H_2O。硅的含量不足导致硅氧四面体层活性氧与层间阳离子的键强增大,促使鱼眼石晶体沿c轴方向的生长,形成粒状—假立方状晶体形态。红外光谱中3 556 cm-1和1 691 cm-1吸收峰以及96.7℃,255.9℃,418.9℃,437.7℃的主要失水温度均表明赤峰鱼眼石中的水属于结晶水,而600℃以后仍有少量的失重,以及红外光谱中3 418 cm-1和3 242 cm-1吸收峰的出现,又反映出赤峰鱼眼石中部分水具有结构水的特点。  相似文献   

16.
A suite of unusual highly skeletal halite pseudomorphs is described from the lower Middle Cambrian rocks that crop out at Ardmore in the Georgina Basin, northern Australia. The pseudomorphs are preserved as both moulds and casts within a dark and light colour-banded chert. They are orientated parallel to bedding and represent halite crystal growth within a brine pool. Laterally equivalent rocks are characterized by sedimentary textures and structures indicative of periodic emergence and desiccation. Laboratory grown halite crystals are also described and compared with the pseudomorphs from Ardmore. Experimentally produced halite crystals formed from either: (1) brine solutions obtained as residues after organic matter extraction from phosphate rocks, or (2) solutions of NaCI and distilled water. Both pyramidal rafted hoppers and floor nucleated cuboids formed in solutions containing only NaCI and distilled water; whereas in the residue solutions, that contained humic acids, rafted pyramidal forms were absent and crystal nucleation was restricted to the floor of the evaporative dish. As brine depth decreased the halite precipitation rate increased and resulted in a suite of excrescent, highly skeletal crystals that formed as a result of brine evaporation to dryness. The variable crystal morphology depended upon both the brine depth and slope of the evaporative dish floor. Horizontally orientated chevron halite crystals formed where the evaporative dish was inclined and precipitation preferentially occurred on cube faces. Pagoda, reticulate ridge and dendritic forms represent an increasingly skeletal crystal suite characterized by the preferential precipitation of NaCI on cube edges and corners rather than faces. Using the experimentally grown crystals as analogues the pseudomorphs at Ardmore are interpreted as forming in very shallow brine pools that evaporated to dryness.  相似文献   

17.
黑铝钙石是一种罕见矿物，在邯邢地区镁铝夕卡岩中，发现一种呈六方片状、黄色半透明的黑铝钙石晶体。本文对该晶体进行了粉晶Ｘ射线、四元衍射、电子探针和红外光谱测量，并认为黑铝钙石是镁铝夕卡岩早期阶段的产物，处在一种富铝、贫硅的地球化学环境和高温条件  相似文献   

18.
以Na2CO3, BaCO3, SrCO3, NH4H2PO4和Eu2O3为原料,利用高温固相反应法合成了Eu3+离子掺杂的磷锶钡钠石(Ba,Sr)(Na,Sr)2Na(PO4)2粉末样品.用X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)、傅里叶变换拉曼光谱(FT-Raman)和扫描电镜(SEM)等技术对其物相组成、结构和晶体形貌进行了表征.探讨了不同晶体结构中Sr/Ba比对晶体结构和发光性能的影响.实验通过对Eu3+的发光特点的表征和研究,分别测试了Eu3+离子的室温激发光谱和发射光谱.研究结果表明:(Ba,Sr)(Na,Sr)2Na(PO4)2属简单六方晶系,所有的振动均来自PO43-阴离子团,Eu3+占据非反演中心的格位,该材料中阳离子位置具有高度扰动性的特点.  相似文献   

19.
Nine beryl samples from Western Carpathians, Slovakia, were investigated by infrared and Raman spectroscopy and differential thermal analysis. Two types of water H2O I and H2O II were detected. Infrared spectroscopy proved the presence of water type I and II in the presence of alkali cations with several bands: (1) symmetric stretching vibration—ν1; (2) antisymmetric stretching mode—ν3; (3) bending vibration—ν2. The presence of singly and doubly coordinated type II water (IIs and IId) was confirmed by single-crystal IR spectroscopy. From Raman spectra a band at 3606 cm?1 was assigned to ν1 of water type I and the range of 3597–3600 cm?1 to water type II. The presence of doubly coordinating water indicates a relatively highly hydrated environment with the presence of alkali ions including Na as the dominant cation coordinated by H2O II. CO2 bands were detected only by single-crystal IR spectroscopy. Thermal analysis proved total water loss in the range of 1.4–2.0 wt% and three main dehydration events. Based on the study of bond-topological arrangements two molecules of H2O IId are each bound with two H···O1 bonds and one Na–OW bond with an angular distortion, and by releasing one H2O molecule more stable H2O IIs is produced. The H2O I molecule is bound only by two equivalent hydrogen bonds. The H2O IIs molecule with a Na–OW bond strength of 0.28 vu and two H···O1 bonds of 0.14 vu without any forced angular distortion is the most stable of all.  相似文献   

20.
Emerald, the green gem variety of beryl (Be3Al2Si6O18), is the third most valuable gemstone after diamond and ruby. The green colour appearance of the crystal is due to trace of Cr3+ and V3+, which replaces Al3+ ions in the crystal lattice of beryl. The hue of green colour of emerald depends on the quantity of Cr3+ and V3+ present in the crystal. Be is incorporated along with Cr and/or V during the process of crystallization. Since Be is relatively rare in the upper continental crust, therefore specific geological and geochemical parameters are required for Be to be incorporated in the crystal lattice of emerald.The present work was carried out to understand the lithological and structural control of emerald occurrences in and around Gurabanda area within the Singhbhum shear zone (SSZ) of Singhbhum crustal province, eastern India. The biotite and serpentine schist belong to the Paleoproterozoic Dhanjori Group and constitute the major lithology of the area. Pegmatite and biotite schist contains a variety of gem minerals in abundance in the area and the gem quality emerald occur at the contact zone of quartz vein and mica-schist. Lithology and structure are the main controlling factors of gem-mineralization in the study area. The study indicates that regional metamorphism and deformation processes along the shear zone played a significant role in the formation of emerald deposits. It is inferred that Singhbhum shear zone facilitated a favourable condition, where the Be bearing pegmatites interacted with Cr bearing mica schist or ultramafic rocks to produce emerald crystal.  相似文献   

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