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1.
苏州高岭土矿主要由高岭石、7埃洛石、10埃洛石及少量绢云母、蒙脱石、明矾石、三水铝石组成。高岭土矿物形成后因外界地化条件改变发生了以下转变:(1)埃洛石脱水向高岭石转化;(2)次生淋滤埃洛石形成;(3)埃洛石和三水铝石之间的互相转化;(4)Ca型蒙脱石形成;(5)高岭土的磷酸盐化作用;(6)次生淋滤明矾石的形成。矿物生成的先后顺序和共生关系可将矿物形成分为主要成矿期和成矿期后演化两个阶段。矿物的后期演化使优质高岭土进一步富集,改造,形成量大质优的高岭土矿。同时,非高岭土矿物的生成又使部分矿石质量变差,降低了矿石的工业价值。 相似文献
2.
用能谱仪初步测试了46个介形虫样品的元素成分,结果表明现代介形虫壳的元素成分变化小,Ca为其主要成分(含Ca94.12—99.8％),Si、Al含量很低。新生代介形虫壳的成分和现代介形虫壳的成分相似.中生代和古生代的介形虫壳含Ca量减少,Si、Al含量增高,还含微量的K、Mn、Fe、S、Mg等元素.介形虫壳成分的变化,推测与地质时期中介形虫的埋藏条件和石化程度等有关. 相似文献
3.
铝土矿和其下部的铁质粘土岩组成铝岩系.铝土矿的铝硅和铝铁均呈反比关系,硅铁呈正比关系,这一特征反映出第一期脱硅,第二期脱铁的两期风化成矿作用.粘土岩的铝含量稳定,铁含量变化大,硅铁是反比关系,显示第二期风化作用,脱出的铁质在粘土岩内沉淀,并生成山西式铁矿.铝岩系具有Al_2O_3/SiO_2和Fe_2O_3/SiO_2两值间同步正相关,显示铝土矿及其母质层粘土岩的陆壳风化成矿. 相似文献
4.
淤泥富含有机质，分解后产生腐殖酸，进而影响淤泥固化效果。仅掺入12%水泥固化淤泥，当标准养护期超过60 d，其强度不增反减。联合掺入3%石灰和12%水泥，固化淤泥的pH值持续180 d处于10.5以上；无侧限抗压强度由750 kPa（养护期28 d）提升到1 500 kPa（120 d），说明借助石灰营造强碱性环境，可以提高水泥固化淤泥的强度；但养护到180 d后，其强度又降到1 250 kPa；钙离子浓度变化规律表明，这是由于腐殖酸溶蚀水泥和石灰的水化胶结物所致。借助偏高岭土卓越的火山灰反应能力，掺入3.0%偏高岭土，提升石灰（3%）?水泥（12%）固化淤泥的耐久性，发现180 d养护期内，其强度始终处于增长趋势，究其原因是偏高岭土富含无定形硅、铝氧化物，具有快速捕获氢氧化钙溶液中钙离子的能力，形成稳定的胶结物，而且不易受腐殖酸的侵蚀作用，证明偏高岭土能够有效提升石灰?水泥固化淤泥长期强度。 相似文献
5.
《矿物学报》2013,(Z1)
Steel slag, a by-product of the steel production industry reaches 10%–15% of crude steel output (Motz and Geiseler, 2001). Their main application lies in the field of building materials due to some containing cementitious components, such as dicalcium silicate (C2S) and tricalcium silicate (C3S) (Waligora et al., 2010). However, blended cements with steelmaking slag show low early hydration activity, low compressive strength and bad durability because steel slag generates above 1600 ℃ with the tense and large grain size crystals, consisting of low content of C2S and C3S and high proportions of f-CaO and f-MgO compared with cement clinker. 相似文献
6.
Plagioclase dissolution related to biodegradation of oil in Brent Group sandstones (Middle Jurassic) of Gullfaks Field, northern North Sea 总被引：1，自引：0，他引：1
Brent Group sandstones from the north side of the Gullfaks Oilfield contain mostly 5–8% albitic plagioclase, whereas plagioclase is almost absent in the same strata in the southern part of the field. Absence of plagioclase throughout the entire vertical extent of the Brent Group in the southern wells seems to rule out provenance as the principal explanation for differing plagioclase content, which is therefore interpreted as the result of diagenesis. Hypotheses for the nature of the inferred leaching event include epigenetic meteoric diagenesis and mesogenetic release of acid components from clay minerals or kerogen, but these explanations are unable to account for the observed spatial distribution of the plagioclase-bearing and plagioclase-free sandstone intervals. However, overall correspondence between the area lacking plagioclase and oil compositions having both anomalously high CO2 and organic geochemical indications of advanced biodegradation suggest a link between plagioclase dissolution and biodegradation of the present oil column. It is, therefore, proposed that acid components from biodegradation selectively reacted with albitic plagioclase to form kaolin, releasing sodium bicarbonate into the residual water. The plagioclase-free sandstones contain more kaolin than the plagioclase-bearing sandstones, as would be expected due to aluminium conservation. However, the wide and overlapping ranges of kaolin content in both groups suggest that most of the kaolin originated from processes other than biodegradation-driven plagioclase alteration, potentially including both epigenetic and mesogenetic dissolution, as well as deposition of detrital kaolin and kaolin precursors. 相似文献
7.
中国的盐湖钾盐资源短缺,导致钾盐消费的对外依存度达50%以上,严重制约农业发展,威胁粮食生产安全。而正长岩型钾资源丰富,K2O品位达8.5%~15.4%,预测资源潜力(K2O)达盐湖钾盐储量的20倍以上。此类矿石钾资源的主要富钾矿物为微斜长石、霞石和白云母,地理上主要分布于中国东部的“秦岭大别正长岩带”和“燕辽阴山正长岩带”。采用电解质溶液热力学软件OLI Analyzer 9.2,对KAlSi3O8-NaOH/KOH/Ca(OH)2-H2O体系相平衡进行模拟,继而对代表性富钾正长岩进行水热碱法分解反应实验,证实K2O溶出率高达85.6%以上。所得硅酸钠钾碱液适于加工多种钾盐或生态型钾肥产品,硅铝组分同时转化为沉淀硅酸钙、钠型/钾型沸石、硅灰石、高岭土等多种工业产品。水热碱法技术的加工过程清洁高效,资源利用率高,环境相容性良好,可为发展绿色可持续的中国钾盐工业新体系提供良好的技术基础。 相似文献
8.
The study of the chemical stability of vitreous material in aqueous media is well‐established. There has to date been little consideration of the implications of variations in the chemical durability of tephra in Quaternary tephrochronology. Chemical alteration can take the form of cationic leaching from the matrix, or complete destruction of the silica network, either of which could constrain the ability to chemically identify distal tephra. Here we apply established models of vitreous durability to the published chemical analyses of a large number of Icelandic tephras in order to predict their relative durabilities under equivalent conditions. This suggests that some important tephras have relatively poor chemical stability, and that rhyolitic tephras are, in general, more stable than basaltic. We conclude that tephras should be expected to show predictable differential chemical stability in the post‐depositional environment. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
9.
The isotope ratios 33S/32S and 34S/32S have been measured in sulphur fractions extracted from samples of the meteorites Allende and Eagle Station by leaching at successively greater acid concentrations and higher temperatures. On a three isotope plot of δ33Sδ34S most of the data lie on or close to the mass fractionation line. The last fraction of sulphur extracted from a bulk Allende sample lies off the line and has an approximately 1%. excess in the 33/32S ratio.Previous searches for anomalous abundance patterns of 32S, 33S, 34S and 36S have been reported by HULSTON and THODE (1965a,b), THODE and REES (1971), and REES and THODE (1972). No isotope abundance variations were found, in the meteorite and lunar samples studied, which could not be explained on the basis of either mass dependent isotope fractionation or, in the special case of iron meteorites, cosmic ray production of 33S and 36S. We report here preliminary results of a renewed search for isotopically anomalous sulphur in which we are concentrating on the Allende and Eagle Station meteorites, both of which contain anomalous oxygen (CLAYTON ., 1973, 1976). In a first attempt to distinguish between normal sulphur and any possible anomalous sulphur, we have leached both bulk samples and hand separated components of these meteorites with hydrochloric acid.CLAYTON and RAMADURAI (1977) suggested that the presence of isotopically anomalous sulphur would be evidence for the existence of presolar grains which are relics of nucleosynthesis in certain zones of supernova expansion. In particular they suggested that sulphides of titanium are good candidates for isotopic analysis. These are not expected to exist in conventional solar equilibrium condensation sequences, but might be abundant in condensates from silicon burning shells of supernovae. Our chemical procedures were already completed when CLAYTON and RAMADURAI'S suggestions came to our attention and it must be stressed that so far, in all cases but one we have examined only sulphur from sulphides which are decomposed by HC1. Thus we may not have sampled sulphides of the type suggested by CLAYTON and RAMADURAI.All samples of the Allende meteorite were ground finer than 50μm before acid extraction of sulphur. Samples of sulphur were extracted from the various phases of the meteorites by using successively stronger hydrochloric acid leaches, longer times and higher temperatures of reaction. Sulphur initially released as H2S was successively converted to CdS, Ag2S and SF6, this latter compound being analysed mass spectrometrically (THODE and REES, 1971). Analyses of nine SF6 samples prepared from Ag2S originally derived from Canyon Diablo troilite were also performed in order to monitor fluorination and mass spectrometry precision and to establish the zero points ofthe isotope variation scales. The results are shown in Table 1. The sulphur contents of the various samples were determined gravimetrically as Ag2S. The bulk and matrix samples are probably a few percent low because of mechanical losses. The percentages of sulphur in each fraction of a sample extracted during each leaching stage are given in the table. The total sulphur content in the bulk and matrix samples of the Allende meteorite i.e., the sum of the sulphur contents of the individual fractions, varies from 1.8 to 2.08%, the highest percentage being in the matrix. These values compare with about 2 to 2.1% obtained by CLARKE . (1970). 相似文献
10.
通过污泥固化技术可以将城市污泥转化为一种新型城市污泥固化土。为了研究污泥固化土工程特性,对新型城市污泥固化土进行无侧限强度试验、收缩特性试验、浸出毒性试验以及X射线衍射试验与微观结构测试。试验结果表明,城市污泥固化土无侧限抗压强度随期龄增加而增长,28 d后基本稳定;新型城市污泥固化土的线缩率随龄期的增大而增大,且28 d后趋于稳定值;与消化后城市污泥相比,城市污泥固化土中的浸出毒性明显减少,重金属浸出量均符合国家规范要求。消化城市污泥衍射峰中氢氧化钙峰值很高,但随着养护期龄的增长,城市污泥固化土中氢氧化钙的衍射峰值减小,碳酸钙的衍射峰值增大,说明固化土各成分反应越充分,强度越高。微结构测试研究表明,污泥固化土SEM图像中有大量的纤维状物质联结着土颗粒和颗粒团块,形成土骨架纤维的交互空间结构,提高了土体强度。 相似文献
11.
近年来,工业和科技的快速发展使得重金属污染土固化/稳定化的修复研究成为热点。运用微生物诱导碳酸钙沉淀(MICP)技术联合吸附材料对锌铅复合重金属污染土进行固化/稳定化的修复,通过无侧限抗压强度试验、毒性浸出试验,评价处理前后污染土的固化效果与重金属的稳定化效果,结合扫描电镜(SEM)和X射线衍射(XRD)等检测手段,揭示MICP技术处理锌铅重金属污染土的修复机制。研究结果表明,采用MICP技术对锌铅重金属污染土进行固化/稳定化之后,可以有效降低污染土中有害重金属的浸出性。当矿化时间为10d时,试样无侧限抗压强度为942.5k Pa;铅的浸出浓度为4.20mg/L,比未处理时降低了44.81%;锌的浸出浓度为4.31mg/L,比未处理时降低了46.19%,效果显著。在此基础上,添加10%的多孔硅吸附材料后,试样无侧限抗压强度可达到1 021 kPa,强度提高了8.3%;铅的浸出浓度为2.45mg/L,与未经处理时相比,降幅达到了67.81%,与单纯MICP方法处理时相比,铅浸出浓度被二次降低了41.67%;锌的浸出浓度仅为2.93 mg/L,与未经处理时相比,降幅达到了63.4%,与单纯... 相似文献
12.
四川盆地飞仙关组气藏硫化氢成因及其依据 总被引：2，自引：0，他引：2
四川盆地东北部下三叠统飞仙关组鲕滩气藏天然气烃类气体以甲烷为主,含量主要分布在75%～90%之间,C2＋含量为0～0.15%;非烃气体以H2S和CO2为主,含量分别为5%～20%和1%～10%。已有观点认为H2S为飞仙关组气藏附近的石膏经硫酸盐热化学还原作用（TSR）而成。随着川东北气区大中型高含硫化氢气田的发现,硫化氢成因机理的研究备受关注。应用金管、高压釜和石英管等实验方法模拟了硫化氢气体的生成,同时检测了模拟生成的硫化氢和石膏、硫磺等硫化物的硫同位素。实验结果表明:硫磺与正己烷在较低温度即可生成大量的硫化氢气体,而正己烷与硫酸钙的反应总体上比较困难,且生成的H2S量较少;富含黄铁矿的低成熟泥灰岩模拟生烃过程中可以生成与甲烷相当,甚至超过甲烷含量的硫化氢气体;含硫化合物与烃类反应生成的硫化氢的硫同位素值比原始物质的硫同位素值重。地层中的SO2－4是海相地层中H2S气体形成的最初来源。含硫烃源岩直接生成高硫化氢天然气和储层中单质硫与烃类的反应是川东北飞仙关组天然气中硫化氢形成的主要原因。 相似文献
13.
The distribution of the clay minerals of the Banco Negro Inferior-Río Chico Group succession (BNI-RC), a middle Danian–middle Eocene mainly continental epiclastic–pyroclastic succession exposed in the Golfo San Jorge Basin, extra-Andean Patagonia (∼46° LS), is assessed in order to determine the possible origin of clay and specific non-clay minerals using X-ray diffraction and scanning electron microscopy analyses. The control over the clay mineralogy of the sedimentary settings, contemporary volcanism, paleoclimate and weathering conditions is considered. A paleoclimatic reconstruction is provided and correlated with the main global warming events that occurred during the early Paleogene.Mineralogical analyses of BNI-RC demonstrate that smectite and kaolin minerals (kaolinite, halloysite and kaolinite/smectite mixed layers) are the main clay minerals, whereas silica polymorphs (volcanic glass and opal) are common non-clay minerals. Throughout the succession, smectite and kaolin minerals are arranged in different proportions in the three clay–mineral assemblages. These show a general vertical trend in which the smectite-dominated assemblage (S1) is replaced by the smectite-dominated assemblage associated with other clays (S2) and the kaolinite-dominated assemblage (K), and finally by S2 up-section. The detailed micromorphological analysis of the clay and non-clay minerals allows us to establish that the origins of these are by volcanic ash weathering, authigenic and pedogenic, and that different stages in the evolution of mineral transformations have occurred.The supply of labile pyroclastic material from an active volcanic area located to the northwest of the study area could have acted as precursor of the authigenic and volcanogenic minerals of the analyzed succession. Diverse fine-grained lithological facies (muddy and tuffaceous facies) and sedimentary settings (coastal swamp and transitional environments, and different fluvial systems) together with variable climate and weathering conditions controlled the mineralogical transformations and the arrangement of clay–mineral assemblages. The paleoclimatic reconstruction suggests a general warm and humid climate. However, the temporal trend of the clay–mineral assemblages, the ratios between smectite and kaolinite and the micromorphological analysis of clay minerals contrasted with evidence from sedimentological analyses suggest a warm and seasonal climate for the basal part of the unit, a warm and humid climate with a relatively more perennial rainfall regime in the middle part of the unit, and a warm and less humid, probably subhumid, climate up-section. Such a reconstruction makes it possible to establish a correlation with some of the hyperthermal events of the Early Paleogene Global Warming (EPGW) and, consequently, constitute one of the most complete time records of the EPGW in South America. 相似文献
14.
The number of mineral species in which a certain chemical element is species-defining (according to statistical data up to 2015) has been specified. Seventy chemical elements are species-defining for 5044 minerals. The following chemical elements lead in the composition of minerals (number of mineral species in parentheses): oxygen (4115), hydrogen (2800), silicon (1471), calcium (1167), sulfur (1056), aluminium (985), sodium (949), iron (945), copper (636), phosphorus (597), arsenic (594), and magnesium (571). The distribution of mineral species by various systems in the products of contemporary fumarole activity at two volcanoes, Tolbachik in Kamchatka, Russia, and Vulcano in Sicily, Italy, has been compared. These locations were also compared for the distribution of species-defining elements. Thus, it has been determined that in fumaroles of both volcanoes, Tl, S, Cl, F and Na are “excessive,” present in minerals in elevated amounts, whereas H, Ca, Fe, and Mn are “deficient.” The abundance of Cu, Se, V, Mg, Zn, As, and F in minerals at Tolbachik is higher than the global mean values of these elements in the Earth’s crust, whereas the abundance is significantly lower at Vulcano. Sn, I, Br, K, Pb, Al, Fe, and Bi demonstrate the opposite behavior. Comparison of the Yadovitaya and Arsenatnaya fumaroles at the Tolbachik volcano showed that the products of the former are richer in H, Cl, Cu, S, K, O, Al, Fe, and Pb, and poorer in As, Ca, Mg, and Na as species-defining elements. In addition, V-and Mo-bearing minerals are found only at Yadovitaya, whereas minerals containing F, Ti, В, Те, and Zn are known only at Arsenatnaya. 相似文献
15.
16.
白云岩酸解法制备轻质氧化镁和碳酸钙实验研究 总被引：1，自引：0，他引：1
以河南卢氏县黄跃沟纯质白云岩为原料,利用盐酸进行分解,制得MgCl2-CaCl2溶液。经过通氨气调节pH值除铁、氨化反应、陈化反应以及碳化反应等过程,制备轻质氧化镁和轻质碳酸钙,研究氨化过程中温度和时间对Mg2+沉淀率的影响,以及碳化时间对碳酸钙制品晶型的影响。采用化学分析方法和扫描电镜分析对制品进行表征,结果表明:轻质氧化镁制品颗粒形貌呈片状,粒径为150 nm左右,其性能达到HG/T2573—2006优等品标准;轻质碳酸钙制品颗粒形貌呈球状,粒径为100 nm左右,其性能达到HG/T2567—1994优等品的标准。实验采用的工艺路线具有能耗低、白云石资源利用率高、加工过程符合清洁生产要求等优点,是白云岩资源高效利用的有效途径之一。 相似文献
17.
《矿物学报》2013,(Z1)
High level waste is nuclear energy generated during the application process ,which is the greatest and the most difficult to management the waste. Proper treatment and disposal of it has already become a worldwide problem, and has become one of the key factors of restricting nuclear energy for sustainable development. Zirconolite (CaZrTi2O7) is one of the most stable mineral on the Earth and actinide major parasitic phase, therefore, it is widely used to solidify actinides separated from high level radioactive waste. In this paper, the zirconolite solid solution was synthesized by high temperature solid-stated method using a particular composition of simulated Np/Pu radioactive incineration ash (SRIA). The phase composition has been investigated by X-ray diffraction (XRD), the calcined temperature gained according to thermogravimetry scanning calorimeter (TG-DSC) analysis. Anti-leaching performance has also been researched with MCC-1 method. Results show that CaZrTi2O7 can load 40% SRIA, the accumulated leaching fraction of Ca is only about 10-4 cm in 28 days at 90 ℃, the concentrations of Zr , Ti and other noble metal ions were all less than detectability of ICP-MS, the leaching rate , normalization leaching rate, and accumulated leaching fraction of all Zr , Ti and other noble ions were 10-8 cm/d, 10-8 g/cm2·d and 10-7 cm, the results indicate that the zirconolite solidification has excellent chemical durability. 相似文献
18.
全风化花岗岩化学及矿物成份在全土和粘粒中的不同表征 总被引：1，自引：0，他引：1
对全风化花岗岩化学和矿物成份的测试常用全土和粘粒部分(粒径<2μm)分别进行。业已发现两者由于物质组成和结构特征的差异,对土工程地质性质所起作用不同。本文给出了6个全风化花岗岩样品的全土和粘粒部分筛分法和移液管法测定粒度成份,用X荧光光谱仪做全量化学分析,及XRD矿物学分析的结果。对比这两部分数据发现,属于含砾土的这些样品化学成份的变化同矿物一致,尤其是同粘土矿物成份含量变化很一致。同全岩相比,粘粒化学成份中的SiO2减少了近50%,K2O含量也降低,而Al2O3、Fe2O3和H2O+都明显升高。粘粒中氧化物相对含量升高者居多;全岩矿物成份以石英、粘土矿物和长石为主,粘粒中埃洛石和高岭石占大多数,其次为伊利石;粒度成份、化学成份和矿物含量相关性比较明显的是:石英和角砾正相关,和砂粒负相关,长石和砂粒正相关,粘土矿物含量和Al2O3、烧失量(LOI)和埃洛石含量正相关。 相似文献
19.
固化铅污染土的干湿循环耐久性试验研究 总被引：2，自引：0，他引：2
在商用高岭土、膨润土与商业黄砂混合物中加入硝酸铅溶液,添加水泥和石灰两种固化剂,采用室内压实制样方法获得固化的铅污染土试样。进行干、湿循环试验,测试固化体的质量损失和无侧限抗压强度等参数随干、湿循环次数的变化规律,评价固化铅污染土的干、湿耐久性。测试结果表明,本试验8种配比的试样都满足干、湿循环的要求;黏土矿物为膨润土的试样干、湿循环耐久性比黏土矿物为高岭土的试样要差;水泥固化土的干、湿循环耐久性要略优于石灰固化土;加入 8 000 mg/kg的铅可略增大土体的抗干、湿循环耐久性。水泥和石灰固化/稳定化重金属污染土时,土体中含水率是保证加固效果的关键参数之一。土体中含水率应能满足固化剂充分水化、水解、火山灰和碳酸化反应之需要。 相似文献
20.
红黏土水敏性强,添加石灰等碱性材料处治后,能获得即刻的改良效果,但由于红黏土呈弱酸性,石灰改良后其长期性能会衰减。为提高石灰稳定红黏土（简称La+L）的长期性能,添加偏高岭土（4%）协同石灰（5%）稳定红黏土（简称La+L+MK）,改善其水敏性和酸?碱互损作用。制备8种初始含水率的压实试样（初始孔隙比相同）,养护到预定时间后开展无侧限抗压强度试验,同时,测定试样的钙离子浓度、电导率和pH值。结果表明：初始含水率为26%左右时,改良土的无侧限抗压强度最高,初始含水率偏高或偏低都不利于改良土的强度增长。究其原因,试样偏干时,缺少水分,石灰水化不充分,不能形成游离态钙离子,无法进行火山灰反应,颗粒之间无法形成胶结;试样偏湿时,火山灰反应形成的胶结强度不及过量水分引起的基质吸力丧失量。试样的钙离子浓度和电导率变化规律,证实了以上原因解释的猜想。当然,添加偏高岭土后,能够显著改善偏湿状态下的石灰土强度。即使浸水饱和后,相对石灰改良土,也能够保持较高的强度,充分证明偏高岭土能够有效降低石灰土水敏性,提高其耐久性。偏高岭土直接提供了大量硅、铝氧化物,且将土体pH值降到有利于硅、铝氧化物溶解的碱性范围,加速火山灰反应,缓减或抑制石灰?红黏土的互损作用。 相似文献