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利用菱镁矿尾矿制备纳米级片状氢氧化镁 总被引：1，自引：0，他引：1
为了对菱镁矿尾矿进行综合回收利用,文中对利用菱镁矿尾矿制备纳米级片状氢氧化镁工艺进行了研究。通过对菱镁矿尾矿的煅烧、与硫酸反应制备硫酸镁以及纳米氢氧化镁的制备工艺和性能表征,成功制备了原始粒径为纳米级、颗粒呈片状的氢氧化镁粉体。利用轻烧镁粉制备硫酸镁溶液的工艺是将轻烧镁粉与水配制成浆料,然后与酸进行反应。反应后控制体系的pH值在5~6,然后进行过滤。制备氢氧化镁的工艺条件为:Mg2+初始浓度为22.75g/L,反应温度为50℃,反应时间为5min,原位表面改性剂为钛酸酯偶联剂YB-502,用量为氢氧化镁质量的1.5%。制得的氢氧化镁结晶情况良好,为片状纳米粉体,其片径100nm左右,片厚10nm左右。氢氧化镁的二次颗粒粒径为d50=0.95μm,d97=3.53μm。 相似文献
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电气石是一种天然的硅酸盐矿物,具有自发极化效应,晶体表面存在静电场,在水处理领域具有广阔的应用前景。本研究利用碳酸钙沉积法考察电气石颗粒的阻垢性能,对投加不同粒径电气石颗粒后产生的碳酸钙钙垢的结构和微观形貌进行分析,探讨电气石颗粒对碳酸钙水溶液结晶性能的影响。实验结果表明,电气石颗粒具有一定的表面阻垢效果,能够降低碳酸钙在水溶液中的溶解度,促使溶液中碳酸钙形成并黏附在电气石颗粒表面,从而抑制碳酸钙钙垢黏附在换热固体表面,且电气石颗粒粒径越小,抑制效果越明显。XRD和SEM分析表明,电气石颗粒能够影响碳酸钙晶体的成核过程,改变碳酸钙的晶体形貌,形成附着性较差的文石型碳酸钙,达到阻垢效果。 相似文献
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现行X射线衍射分析黏土矿物都是提取粒径小于2μm的悬浮溶液检测样品的黏土矿物组合及含量,含量数据有时与其他检测数据相悖。在鄂尔多斯盆地黏土矿物研究中,通过偏光显微镜和扫描电镜发现存在粒径大于2μm的黏土矿物颗粒,特别是高岭石的粒径多为3～10μm,这些大颗粒黏土矿物会造成含量数据不准确。为了证明大颗粒黏土矿物对其含量测量的影响,本文设计了不同粒径标准的提取物对比试验:随机选取267个样品,每个样品分别按照10μm和2μm标准提取两份悬浮溶液制成测试片,采用SY/T5163—2010行业标准中的检测方法得到10μm和2μm提取物的黏土矿物组合及含量。通过对比发现大颗粒黏土矿物对各类黏土矿物的相对含量测量结果有明显影响:10μm提取物中高岭石含量明显增大;伊利石/蒙脱石间层矿物含量显著降低;伊利石含量的变化小且无规律;绿泥石含量整体变化较小,少量样品中绿泥石含量发生了明显的偏离,与大颗粒高岭石的赋存有关。本研究提出应结合地质状况和工作目的审慎选择提取粒径的标准,对SY/T 5163—2010中的黏土矿物提取粒径标准作出修订。 相似文献
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川北地区中三叠统层序地层学的对比研究表明,雷口坡组顶界面(T2/T1界面)和底界面(T3/T2界面)具有横向分异规律,由此识别出2个Ⅲ级层序,其上部SQ2层序普遍缺失高水位体系域。层序地层格架内的岩相古地理分析表明,该区中三叠世长期处于蒸发台地、局限台地环境,碳酸盐岩颗粒结构欠发育,可见少量藻屑颗粒灰岩和白云岩、细—中晶白云岩,缺少生物礁标志,藻席大量发育,白云石化作用强烈。识别出了工农镇剖面斜坡角砾,并对台地边缘位置进行了厘定。根据沉积及岩石学研究结果,得出了川北地区中三叠统典型的陡坡封闭型镶边台地模式。 相似文献
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介孔TiO2分子筛的复合模板合成 总被引：2，自引：0，他引：2
以钛酸异丙酯为钛源,吐温-60和十二胺为复合模板剂,通过控制反应液的pH值,采用溶胶-凝胶(Sol-G el)工艺合成出介孔T iO2前驱体,并通过热处理除去模板剂,得锐钛型介孔T iO2。合成产物采用粒度分布、SEM、TEM、XRD及等温N2吸附进行分析表征。研究表明:以硫酸为水解抑制剂,控制体系pH值为3,可以有效抑制钛酸异丙酯(TT IP)的水解缩聚速率,合成前驱体经热处理脱模后得锐钛型介孔T iO2,孔道有序度提高,介孔孔道收缩变小,晶粒尺寸L101=11.02 nm;颗粒粒度分布变窄,粒径减小,平均粒径为0.587μm;介孔T iO2孔径分布窄,平均孔径为4.0 nm,BET比表面积为143.2 m2/g,孔容0.16cm3/g。 相似文献
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川中磨溪—高石梯地区栖霞组发育滩相白云岩,目前对滩相中差异白云石化机理不明确,导致难以预测优质白云岩储层的分布。在岩石学和地层特征研究基础上,通过分析不同类型白云岩的微量元素及碳、氧、锶同位素特征,结合颗粒滩类型和构造背景,系统研究了该区不同类型白云岩的成因机理及模式。结果显示:研究区栖霞组白云岩中白云石以细晶为主,中晶和粗晶次之,晶形多为半自形—自形。白云岩具有明显的残余颗粒结构,表明原始岩性为颗粒灰岩。细晶、细—中晶白云岩的阴极发光整体较暗,呈暗红色至红色,稀土元素配分模式与同期灰岩相似,白云岩的87Sr/86Sr比值大部分落于二叠纪海水的87Sr/86Sr比值范围之内,表明白云岩的成岩流体与海水沉积的灰岩具有同源性。白云岩的δ13C值（3.73‰~4.19‰）与同期灰岩δ13C值（3.61‰~4.93‰）相近,表明白云岩与灰岩具有一致的碳源。从灰岩到白云岩,Sr含量明显减少且Mn含量有所增加,说明灰岩经过一定的成岩作用被交代形成白云岩,该类白云岩为埋藏条件下地层中富Mg2+的流体交代孔隙型颗粒灰岩而成;中—粗晶白云岩的阴极发光呈红色,具明显环带特征,且具有高的Mn含量、低Sr/Ba比值及铕的正异常,87Sr/86Sr比值高于同期海水值,δ18O值在-8.06‰~-8.52‰,为颗粒灰岩在埋藏期受持续、充足的云化流体供给而成,较高的包裹体均一温度和δ18O值明显偏负均指示埋藏白云化作用过程还受到局部高温的影响。总体而言,埋藏白云岩化是该区白云岩的主要成因,地层中富镁的流体在压力和热对流的双重影响下进行迁移,促进白云岩化流体的运移,但局部地区鞍形白云石的形成遭受了后期不同程度的热液改造作用。 相似文献
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《海相油气地质》2015,(4)
以川西北地区矿2井为例,对井筒尺度的储层结构进行了高精度刻画。以成像测井为主要手段,在地质标定的基础之上,建立了川西北栖霞组白云岩储层的标准剖面,有效识别出主要的5种岩石类型(生物碎屑灰岩、"豹斑"白云质灰岩、块状中—粗晶白云岩、斑状中—粗晶白云岩和角砾状白云岩)和4种储集空间类型(溶蚀孔洞、晶间孔、扩溶缝和构造缝)。研究表明川西北栖霞组白云岩发育多重孔隙系统,其中,溶蚀孔洞是最主要的储集空间类型,普遍呈层状或准层状,发育于块状中—粗晶白云岩中,共1层厚39.5 m;晶间孔是次一级的储集空间类型,发育于斑状中—粗晶白云岩中,共4个薄层,平均厚1.1 m;另外两种储集空间类型(扩溶缝和构造缝)零星发育,对储集性能的贡献不大。块状中—粗晶白云岩发育于三级层序高位域,斑状中—粗晶白云岩仅发育于高位域中四级层序向上变浅旋回的顶部。 相似文献
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滑石的颗粒粒径、形貌、晶型等对其应用的实效性、终端产品的性能产生极大影响,目前主要研究其表面改性,而有关微观形貌及晶体结构研究较少。本文利用X射线荧光光谱、X射线衍射分析、红外光谱、粒度分析仪结合高分辨场发射扫描电镜(FE-SEM)技术对辽宁滑石粉在高强度机械力研磨作用下的微形貌和晶体结构变化特征进行系统研究。结果表明滑石粉原矿混合物中MgO与SiO2的分子个数比约为0.45,该数值明显低于纯滑石粉晶体中MgO与SiO2的分子个数比0.75。此类滑石为典型的单斜晶系,研磨作用使滑石粉由晶态转变为非晶态结构,其层状结构的有序化和键合作用发生了明显的变化。滑石粒度随研磨时间变化呈现减小-增大-减小的循环过程。研磨后粉体形貌存在差异,细化的小颗粒粉体因团聚而呈"准球体",且随着研磨的进行出现细化-团聚-细化的反复过程。此结论对于滑石的深加工与应用及其相关矿物粉体的研究具有一定的参考价值。 相似文献
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颗粒形貌是影响珊瑚砂力学性质的重要参数,研究珊瑚砂多尺度形貌特征有助于从细观角度阐释其力学特性。基于颗粒动态图像分析技术对不同粒径范围内超过20万个珊瑚砂和陆源石英砂（包括人工破碎石英砂和天然石英砂）颗粒开展颗粒形貌扫描和对比分析,提出了适用于珊瑚砂的颗粒形状分类标准,并从颗粒形状、磨圆度和凸度3个尺度上揭示了海相珊瑚砂与陆源石英砂颗粒形貌的差异性。结果表明：（1）珊瑚砂主要由块状、片状及棒状3种类型的颗粒组成,以伸长率和扁平率为0.5作为珊瑚砂颗粒形状的划分阈值进行颗粒形状分类,该分类方法的准确率可达90%。（2）珊瑚砂中块状颗粒占比最大,且含量大于50%。随着粒径增加,块状颗粒占比增加,片状颗粒占比下降,而棒状颗粒基本维持不变;随着粒径的增加,石英砂中的块状颗粒占比高于珊瑚砂,这是由颗粒的矿物性质决定的,而与颗粒的风化破碎方式无关。（3）人工破碎石英砂的磨圆度与珊瑚砂的较为接近,且略小于天然石英砂。块状颗粒的磨圆度大于片状颗粒,更大于棒状颗粒,因此块状颗粒占比越高,集合体的磨圆度越大。（4）珊瑚砂的颗粒凸度介于0.85～1.00间,石英砂的凸度大于珊瑚砂。随着粒径的增加,珊瑚砂的凸... 相似文献
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中国金属镁工业的环境效应与可持续发展 总被引：5，自引：1，他引：4
中国的优质白云岩、菱镁矿资源丰富,为发展金属镁工业提供了良好条件。20世纪90年代末,以相对浪费能源、资源和牺牲区域环境质量为代价,依赖皮江法炼镁技术,中国发展成为世界上金属镁生产和出口的第一大国。现今中国社会和经济发展面临的能源、资源和环境挑战,决定了必须对皮江法炼镁技术进行变革,以实现金属镁工业的清洁生产和节约发展。以优质白云岩为原料,经煅烧和钙镁分离,生产轻质碳酸钙和氧化镁,进而采用碳热还原法提取金属镁的技术,较之传统的皮江法具有资源利用率高、节能高效、且可完全实现清洁生产等优势。这一创新技术体系,将在现今中国国情背景下,引导金属镁工业步入可持续发展之路,符合建立资源节约型、环境友好型国家的要求。 相似文献
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Precipitation of dolomite using sulphate-reducing bacteria from the Coorong Region, South Australia: significance and implications 总被引：9，自引：0，他引：9
Dolomite was successfully precipitated in culture experiments that simulated microbiogeochemical conditions prevailing during late stages of evaporation in ephemeral, hypersaline dolomitic lakes of the Coorong region, South Australia. Analyses of lake- and pore-water samples document rapid geochemical changes with time and depth in both dolomitic and non-dolomitic lakes. Extremely high sulphate and magnesium ion concentrations in lake waters decline rapidly with depth in pore waters throughout the sulphate-reduction zone, whereas carbonate concentrations in pore waters reach levels up to 100 times those of normal sea water. Ultimately, sulphate is totally consumed and no solid sulphate is recorded in the dolomitic lake sediments. ‘Most probable number’ calculations of lake sediment samples record the presence of large populations of sulphate-reducing bacteria, whereas sulphur-isotope analyses of lake-water samples indicate microbial fractionation in all the lakes studied. Viable populations of microbes from the lake sediments were cultured in anoxic conditions in the laboratory. Samples were then injected into vials containing sterilized clastic or carbonate grains, or glass beads, immersed in a solution that simulated the lake water. Falls in the levels of sulphate and rising pH in positive vials were interpreted as indicating active bacterial sulphate reduction accompanied by increased concentrations of carbonate. Within 2 months, sub-spherical, sub-micron-size crystals of dolomite identical to those of lake sediments were precipitated. It is concluded that bacterial sulphate reduction overcomes kinetic constraints on dolomite formation by removing sulphate and releasing magnesium and calcium ions from neutral ion pairs, and by generating elevated carbonate concentrations, in a hypersaline, strongly electrolytic solution. The results demonstrate that bacterial sulphate reduction controls dolomite precipitation in both the laboratory experiments and lake sediments. It is proposed that dolomite formation, through bacterial sulphate reduction, provides a process analogue applicable to thick platformal dolostones of the past, where benthic microbial communities were the sole or dominant colonizers of shallow marine environments. 相似文献
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HILARY IRWIN 《Sedimentology》1980,27(5):577-591
In the argillaceous sequence of Kimmeridge Clay a carbonate rich bed is composed of ferroan dolomite cement with varying amounts of excess CaCO3, and Fe2+ substitution in the Mg2+ sites. The isotopic and chemical compositions change symmetrically about the centre of the band proving that it grew by vertical accretion during diagenesis. Textural and isotopic evidence shows that growth centred on a horizon rich in primary carbonate which became dolomitized and assimilated during production of diagenetic carbonate. This accounts for the lateral extent of the concretion. Early central diagenetic carbonate was produced from organic matter by bacterial fermentation (δ13C =+0.59‰) and later marginal carbonate by abiotic breakdown, (δ13C tending towards — 2.73‰). δ18O values range from — 1.56 to — 4.46‰ because the dolomite precipitated during progressive burial. As burial increased, magnesium, whose dominant source was trapped seawater, became depleted while the relative availability of Fe2+, whose source was dominantly reduced detrital oxides, increased. Dolomitization and the source of diagenetic components for dolomite formation are discussed. Diffusion and pore fluid migration transported ions to the site of precipitation. Early cementation of the band served to influence pore fluid migration, but thereafter pore fluid migration controlled carbonate precipitation. 相似文献
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Holocene carbonate sedimentation in Lake Manitoba, Canada 总被引：1，自引：0，他引：1
W. M. LAST 《Sedimentology》1982,29(5):691-704
The carbonate mineral suite of the modern offshore bottom sediment of the South Basin of Lake Manitoba consists mainly of high magnesian calcite and dolomite with minor amounts of low-Mg calcite and aragonite. The high-Mg calcite is derived from inorganic precipitation within the water column in response to supersaturation brought about by high levels of organic productivity in the basin. Both dolomite and pure calcite are detrital in origin, derived from erosion of the surrounding carbonate-rich glacial deposits. Aragonite, present only in trace amounts in the offshore sediments, is bioclastic in origin. The upward increase in the amount of magnesian calcite in the post-glacial sediment record is attributed to increasing photosynthetic utilization of CO2 in the lake. Stratigraphic variation in the amount of magnesium incorporated into the calcite lattice is interpreted as reflecting a variable magnesium input to the lake from ground water and surface runoff, and possibly variable calcium removal in the precipitating lake water. The effects of long-term chemical weathering at the source and size segregation explain the changes in dolomite content throughout the section. 相似文献
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用化学物相分析法测定瓮福磷尾矿中钙、镁、磷元素形态含量。结果表明,磷尾矿中钙主要以白云石的形式赋存,并有少量以方解石、磷酸盐形式存在;镁主要以白云石的形式赋存,并有少量以磷酸盐、硅酸盐形式存在;磷主要以磷灰石的形式赋存,并有少量以铁氧化物、独居石、磷钇矿形式存在。各元素形态加标回收率为97.6%~107.2%,相对标准偏差(RSD,n=12)为0.77%~4.85%。各元素形态分析结果表现出较好的稳定性,表明采用化学物相分析法测定瓮福磷尾矿中钙、镁、磷元素形态含量结果准确可靠。 相似文献
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Holocene dolomite forms in the sediment of Lake Hayward, a small permanent hypersaline lake in the Clifton-Preston Lakeland System, Western Australia. The geomorphological setting of dolomite formation in Lake Hayward is similar to the Coorong region in South Australia. Unlike in the Coorong region, dolomite in Lake Hayward does not form as a direct precipitate from the lake water, but is of diagenetic origin. This can be deduced from the following features: (1) the dolomite occurs only below 60–70 cm from the sediment-water interface, (2) dolomite occurs as luminescing cement, and (3) dolomite has pristine well-formed rhomb-shaped crystals. The source of magnesium for dolomitization is probably from the concentration on inflowing groundwater by evaporation and the selective removal of calcium by chemical and biological aragonite/calcite precipitation. 相似文献
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Palygorskite is a fibrous, magnesium‐bearing clay mineral commonly associated with Late Mesozoic and Early Cenozoic dolomites. The presence of palygorskite is thought to be indicative of warm, alkaline fluids rich in Si, Al and Mg. Palygorskite has been interpreted to form in peritidal diagenetic environments, either as a replacement of detrital smectite clay during a dissolution–precipitation reaction or solid‐state transformation, or as a direct precipitate from solution. Despite a lack of evidence, most diagenetic studies involving these two minerals posit that dolomite and palygorskite form concurrently. Here, petrological evidence is presented from the Umm er Radhuma Formation (Palaeocene–Eocene) in the subsurface of central Qatar for an alternative pathway for palygorskite formation. The Umm er Radhuma is comprised of dolomitized subtidal to peritidal carbonate cycles that are commonly capped by centimetre‐scale beds rich in palygorskite. Thin section, scanning electron microscopy and elemental analyses demonstrate that palygorskite fibres formed on both the outermost surfaces of dissolved euhedral dolomite crystals and within partially to completely dissolved dolomite crystal cores. These observations suggest that dolomite and palygorskite formed sequentially, and support a model by which the release of Mg2+ ions and the buffering of solution pH during dolomite dissolution promote the formation of palygorskite. This new diagenetic model explains the co‐occurrence of palygorskite and dolomite in the rock record, and provides valuable insight into the specific diagenetic conditions under which these minerals may form. 相似文献
19.
John P. Armstrong Mark Wilson Robert L. Barnett Tom Nowicki Bruce A. Kjarsgaard 《Lithos》2004,76(1-4):415-433
A suite of fresh, Late Cretaceous to Eocene hypabyssal kimberlites from the Lac de Gras field were studied in order to understand better carbonate, silicate and oxide paragenesis. The samples have excellent preservation of textures and primary mineralogy and are archetypal or Group 1 kimberlite. Five kimberlite localities are identified as calcite-bearing based on the presence of high Sr–Ba calcite as phenocrysts, microphenocrysts and in segregations. Three kimberlite localities are identified as dolomite-bearing based on the presence of mixed calcite–dolomite segregations containing oscillatory and banded textures of calcite–dolomite solid solution and dolomite (±magnesite). Sr–Ba calcite are characterized by high XCa (>0.95) and are enriched in Sr (4900–11,100 ppm) and Ba (3200–14,200 ppm). The calcite–dolomite and dolomite–magnesite solid solution compositions span the XCa range from 0.42 to 0.95, and typically have Sr and Ba contents in the range of 1000–4000 ppm. The carbonate, silicate and oxide mineral compositions suggest that the origin of the calcite-bearing versus dolomite-bearing kimberlites studied is related to subtle differences in parent magma composition, in particular, the CO2/H2O ratio. Formation of the carbonates reflects the latter part of a protracted magmatic crystallization sequence, in which Sr–Ba calcite precipitates from an evolved kimberlite melt. Subsequently, calcite–dolomite solid solution and dolomite is precipitated from localized, Mg-rich carbonate fluids at relatively high temperatures (higher than serpentine stability). 相似文献
20.
Dirk Schulze-Makuch Philip Goodell Thomas Kretzschmar John F. Kennedy 《Hydrogeology Journal》2003,11(3):401-412
Groundwater of the southern Jornada del Muerto Basin, an intermontane basin structure associated with the Rio Grande rift
located in south-central New Mexico, USA, was analyzed chemically and microbially. A microbial phospholipid fatty acids (PLFA)
analysis revealed a sparse microbial population consisting of relatively simple microorganisms with no major population changes
along the flow system. A nucleic acid (DNA) analysis of the groundwater resulted in the identification of ten eubacterial
and one archeal species. Chemical analyses revealed that sulfate along with calcium, magnesium, iron, and manganese is removed
by about an order of magnitude in concentration from the recharge area to the discharge area. The removal of iron, manganese,
magnesium, and to some extent calcium can be explained by oxidation reactions and the precipitation of dolomite. Sulfate and
additional calcium are most likely removed by the precipitation of gypsum. Thiobacillus spp. are oxidizing metal sulfides that occur as subsurface sulfide mineral deposits to sulfuric acid, which subsequently
reacts with calcium carbonate and water to precipitate gypsum. The presence of these sulfide deposits exposed to oxygenated
water in the deep groundwater flow system significantly alters its chemical and bacteriological composition.
Electronic Publication 相似文献