江西新余铁矿的地球化学特征及其与华北BIFs铁矿的对比

本文报道了新余和华北BIF铁矿的主量元素、微量元素、稀土元素的测试结果:新余和华北地区BIF铁矿的化学成分均主要由Fe2O3T和SiO2组成,它们的页岩标准化稀土元素配分曲线均呈现轻稀土亏损、重稀土富集的分馏模式。与华北BIF相比,新余铁矿具有更高的Al2O3和TiO2含量、微量元素含量、稀土总量,以及更低的Eu异常和Y/Ho比值,这些特征均表明,与华北地区相比,高温热液对新余地区BIF的贡献不明显。铁矿无明显的Ce负异常和Fe同位素组成为正值的特征暗示了铁矿沉淀时的海水为低氧逸度环境。     

辽宁本溪大台沟铁矿床地球化学特征及成因探讨

为探讨辽宁大台沟铁矿床的成矿物质来源及形成环境,选取典型铁矿石5块进行主量元素、微量元素和稀土元素分析测试。结果显示:大台沟铁矿床保存有明显的化学沉积特征,化学成分主要由Fe_2O_3,FeO和SiO_2组成(Fe_2O_3+FeO+SiO_2=87.33%～96%),其他组分(MnO,MgO,CaO,Na_2O,K_2O,TiO_2,P_2O_5,Al_2O_3)含量较低;页岩标准化后的稀土元素配分曲线显示为稀土总量低(ΣREE平均为19.65×10^-6),轻稀土元素相对亏损,重稀土元素相对富集;且具有一定的Eu(Eu/Eu~*=1.52～2.72),Y(Y/Y~*=1.18～1.52),La(La/La~*=1.17～2.26)的正异常,弱的Ce(Ce/Ce~*=0.79～0.92)异常;Y/Ho值平均34.19接近于海水的分布范围;Sr/Ba值平均1.79,属于火山岩和海相沉积物;Ti/V值平均38.84,属于火山建造。这些特征表明:该矿床的形成可能与海相火山沉积物有关,属于火山沉积变质型铁矿范围;成矿物质来源于热水和海水的混合作用;矿床形成于相对于缺氧的环境。     

冀东杏山BIF铁矿形成时代及成因探讨

杏山BIF型铁矿位于冀东曹庄一带,矿体赋存于太古界三屯营组变质岩系中。矿石多为条纹-条带状构造,其围岩和夹层以斜长角闪岩为主,兼具少量黑云石英片岩和黑云钾长片麻岩。对BIF铁矿进行的地球化学分析表明,条带状铁矿石富集重稀土((La/Yb)*PAAS平均0.46),Eu正异常(Eu/Eu*PAAS平均2.19)、La正异常(La/LaPAAS平均2.14)和Y的正异常(Y/Y*PAAS平均1.85)明显,加之高的Y/Ho值(平均46.81),说明成矿物质来源于海底高温热液与周围海水的混合溶液;无Ce的负异常说明BIF形成于低氧逸度环境;BIF显示较低的Al2O3和TiO 2含量,且二者缺乏相关性,说明在BIF沉淀过程中几乎没有陆源碎屑物的加入。对矿体围岩斜长角闪岩、黑云石英片岩及黑云钾长片麻岩的原岩恢复,表明斜长角闪岩的原岩为玄武岩-安山质玄武岩,黑云石英片岩及黑云钾长片麻岩的原岩可能为泥质碎屑岩。元素地球化学分析表明,黑云钾长片麻岩具有较低的总稀土含量(59.46×10-6~66.99×10-6)、不明显的Eu负异常(Eu/Eu*=0.77~0.91)、略微的Th和U富集、无Nb和Ta的亏损;而黑云石英片岩具有较高的稀土总量(168.7×10-6~171.0×10-6)、强烈的轻稀土富集((La/Yb)N=6.81~7.07)和较弱的Eu负异常(Eu/Eu*=0.64~0.68),两者不一致的地球化学特征说明他们具有不同的物质来源。斜长角闪岩与N-MORB具有相似的特征,如富集大离子亲石元素(LILEs),亏损Th和U、Nb、Ta、Ti、Zr和Hf等无明显亏损。综合分析表明斜长角闪岩的母岩浆来源于尖晶石二辉橄榄岩30%的部分熔融,且其母岩浆在分异结晶过程中可能受到陆壳物质的混染。对矿体夹层斜长角闪岩LA-ICP-MS锆石U-Pb定年,结果表明其原岩形成于2859±22Ma至2491±13Ma之间,最有可能形成于新太古代晚期,这间接约束了杏山BIF型铁矿的形成时代,暗示着迁西岩群主体可能仍形成于新太古代晚期。而2859±22Ma的捕掳锆石年龄反映杏山-曹庄地区可能存在有中太古代表壳岩。     

冀东司家营条带状含铁建造铁矿石铁同位素特征及其地质意义

司家营条带状含铁建造（Banded iron formation,BIF）型铁矿床是冀东地区规模最大的铁矿床,前人对其进行了大量的年代学、岩石学和元素地球化学工作,但目前尚未对其进行Fe同位素研究。本文通过Fe同位素和主微量、稀土元素相结合的方法对司家营BIF的成矿物质来源和形成背景提出了有效制约,同时对司家营BIF的锆石U- Pb年龄数据进行补充。锆石U- Pb年代学显示,司家营BIF形成于2537~2531Ma。地球化学数据显示司家营BIF矿石主要由TFe2O3和SiO2组成,具有较低的Al2O3和TiO2含量,富集Fe重同位素（δ56Fe=0.341‰~0.525‰）;稀土元素配分模式呈现轻稀土亏损、重稀土富集的特征,具有明显的Eu、Y、La正异常,Y/Ho比率较高（Y/Ho=34.96~45.84）。这些特征表明司家营BIF是基本无碎屑物质参与的化学沉积岩,稀土元素来源于高温热液和海水的混合溶液,铁质来源于海相热液流体。司家营BIF缺乏真正的Ce负异常和Fe同位素组成均为正值指示其形成于缺氧环境。综合对比世界上其他地区太古宙BIF的Fe同位素特征,本文认为新太古代时期地球海洋含氧量逐步上升,此时海洋总体属于缺氧环境,但部分地区氧气含量较高。     

河南舞阳经山寺铁矿床地球化学特征及其地质意义

河南经山寺铁矿床位于华北板块南缘,矿体形态为似层状和透镜状,铁建造以条带状铁矿石为主,含有少量的块状矿石,其顶、底板围岩及矿体夹层主要为太华群铁山庙组大理岩。矿床地球化学分析结果表明,本区条带状铁建造是与海相火山沉积有关的前寒武纪火山沉积变质型铁矿。Sr/Ba平均值20.55,Ti/V平均值104.24,Ni/Co平均值2.31,Y/Ho平均值62.67,具La的正异常(La/La*=0.807~1.564),Eu的正异常(Eu/Eu*=1.246~2.821),Y的正异常(Y/Y*=2.426~3.310),反映出经山寺条带状铁矿床形成于火山热液和海水混合的环境。极低的Zr、Hf、Th含量,表明陆源碎屑物质对BIF的贡献极少。无明显Ce负异常(Ce/Ce*=0.809~0.955),揭示条带状铁建造沉积于海水缺氧环境。流体包裹体均一温度主要集中在150~320℃,成矿流体具有低盐度〔w(NaCleq)=2.07%~18.80%〕、低密度(0.846~0.979 g/cm3)特征,流体包裹体成分显示成矿热液是一种低盐度的Na+、Cl-型水,并含有较高的CO2。经山寺铁矿床经历了海底火山喷流沉积和区域变质作用2个成矿期,成矿流体具多源性,且发生过强烈的不混溶作用,影响铁质发生进一步的迁移和富集。     

河南舞阳铁山庙式BIF铁矿的矿物学与地球化学特征及对矿床成因的指示

河南舞阳铁矿位于华北克拉通南缘.铁山庙式铁矿是舞阳铁矿的一部分,赋存于新太古界太华杂岩铁山庙组表壳岩中.本文根据铁山庙式铁矿中三种不同类型矿石(条带状石英-辉石-磁铁矿、块状辉石-磁铁矿、块状石英-磁铁矿)中磁铁矿的矿物成分、全岩/矿的主量元素及微量元素特征,探讨铁山庙式铁矿床的成因.磁铁矿单矿物成分分析表明,条带状石英-辉石-磁铁矿矿石中磁铁矿的FeOT含量90.6％ ～93.1％,平均91.8％;块状辉石-磁铁矿矿石中磁铁矿的FeOT含量90.7％～91.2％,平均91.0％;块状石英-磁铁矿矿石中磁铁矿的FeOT含量92.0％～93.0％,平均92.4％.上述平均值均与磁铁矿FeOT的理论值(93.1％)接近.三种类型矿石的其它元素如TiO2、MgO、MnO、CaO、Al2O3 Cr2O3 NiO等含量均＜0.1％,无明显区别,表明该区磁铁矿为含杂质极少的纯磁铁矿,表现出沉积变质成因磁铁矿的特征.矿石中斜方辉石-单斜辉石及近矿围岩紫苏辉石-长石-石英矿物组合,表明铁山庙式矿床经受了高级变质作用,石英、磁铁矿等矿物普遍发生变质重结晶,颗粒粗大,但仍保存原有的地球化学组成.元素地球化学分析显示,三种类型矿石中SiO2 、TiO2 Al2O3、P2O5的含量相近;块状辉石-磁铁矿较其它二者相对贫铁、富钙、镁,这是由于块状辉石-磁铁矿石中富含铁普通辉石和铁次透辉石所致;矿石中TiO2、Al2O3含量都极低,说明该区成岩成矿过程中未受到碎屑物质的混染.三种不同类型矿石的主量元素含量总体上都与世界典型BIF的相近.对于稀土元素,三种类型矿石均具有轻稀土亏损、重稀土富集((La/Yb)PAAS=0.29～0.995＜1),La、Eu、Y的正异常(La/La*=1.10～1.89;Eu/Eu* =1.30～2.23;Y/Y* =1.47～1.84),较高的Y/Ho比值(39.7 ～51.3),具有现代海水及高温热液混合特征.因此,我们认为铁山庙式铁矿三种不同类型的矿石是极少受到陆源碎屑混染的化学沉积成因,虽遭受后期变质作用,但仍属BIF型铁矿.     

冀东、五台和吕梁地区条带状铁矿的稀土元素特征及其地质意义

详细报道了冀东、五台和吕梁地区条带状铁矿全岩样品的稀土元素分析结果。结果表明,研究区BIF具有非常相似的特征：稀土总量均较低;经页岩标准化的稀土元素配分模式均呈现轻稀土亏损、重稀土富集的特征;Y/Ho比值较高;具有明显的Eu、Y、La的正异常,且这些特征表明研究区BIF的稀土元素来源于火山热液和海水的混合溶液。虽然BIF均显示Eu正异常,但不同类型、不同沉积年龄BIF的铕异常程度不同：与吕梁地区Superior型铁矿相比,冀东和五台地区的Algoma型铁矿显示了更大的Eu正异常;并且自中太古代-新太古代-古元古代,BIF的铕正异常逐渐减小,这可能反映了随着BIF沉积年龄的减小,进入到该地区海水中的高温热液流体逐渐减少;同时,研究区BIF缺乏明显的Ce负异常,可能暗示在BIF沉积时海水的氧化还原状态为缺氧环境。     

鞍山-本溪地区条带状铁矿的Fe同位素特征及其对成矿机理和地球早期海洋环境的制约

本文报道了鞍山-本溪地区晚太古代条带状铁建造的主量元素、微量元素、稀土元素和Fe同位素的分析结果.结果显示:铁矿主要由Fe2O3T和SiO2组成,具有较低的Al2O3和TiO2含量;微量元素含量和稀土总量均较低;经页岩标准化的稀土元素配分模式呈现轻稀土亏损、重稀土富集;具有明显的La、Eu、Y的正异常;较高的Y/Ho比值.这些特征均表明鞍山-本溪地区条带状铁矿是由极少碎屑物质加入的化学沉积岩,成矿物质主要来源于海底热液的贡献.相对于标准物质IRMM-014,条带状铁矿石的Fe同位素组成最突出的特征是均为正值,这是由于二价铁溶液经部分氧化和沉淀形成富集重铁同位素的三价铁氧化物或氢氧化物的结果,且沉淀程度的不同是控制Fe同位素组成变化的重要因素.条带状铁矿无明显的Ce负异常和Fe同位素组成为正值的特征暗示了铁矿沉淀时的海水为低氧逸度环境.     

河南舞阳铁山铁矿床地球化学特征及其地质意义

河南舞阳铁山铁矿床为新太古代大型鞍山式铁矿床,本文对铁山矿床进行了岩石学、地球化学方面的研究,并与国内外该类型矿床进行了对比。通过对铁山铁矿床赋矿围岩和矿石的地球化学分析,得出本区条带状硅铁建造可能与海相火山沉积物有关,属前寒武纪火山沉积变质型铁矿床。流体包裹体测温结果表明,含矿围岩中的包裹体均一温度集中在120³60℃之间,矿石中包裹体均一温度峰值为120³20℃,成矿流体具有低盐度[w（NaCl）为1%¹4%]、低密度（0.75¹.00g/crn³）特征。成矿溶液是一种低盐度的Na⁺、Ca²⁺、SO₄^2-、Cl^-型水,并含有较高的CO₂和一定量的O₂、N₂及少量CH₄。岩石学研究结果认为其经受了绿片岩相至低角闪岩相变质作用,磁铁矿部分受到变质重结晶,但局部仍保存有化学沉积的特征。在TFe-（CaO+MgO）-SiO₂图解中,其分布与鞍山、五台山条带状铁矿和世界条带状铁矿分布区一致。铁山矿床稀土元素含量较低,具有太古宙海洋沉积的特征,在PAAS（太古宙后平均澳大利亚沉积岩）标准化的稀土配分曲线中显示轻稀土的相对亏损和重稀土的相对富集,具有明显的Eu正异常（Eu/Eu*=0.30².21）和明显的Y正异常（Y/Y*=1.34³.19）,具有一定的La正异常（La/La*=0.81¹.60）和轻微Ce负异常（Ce/Ce*=0.87¹.01）,这一特征与我国鞍山弓长岭和五台山及世界许多地区的太古宙BIF特征一致。微量元素中Ti、V、Co、Ni、Mn、Sr、Ba等元素的含量都较低,在原始地幔标准化的微量元素配分曲线中具U、Ta、La、Ce、P正异常,K、Nb、Sr、Hf、Zr负异常。对铁山条带状铁矿中Sr/Ba、Ti/V等元素的比值与其他地区进行了对比。综合研究结果认为铁山条带状铁矿具有与火山热液伴生的铁质,形成于缺氧的海洋化学沉积环境。铁矿床经历了前期含硅铁沉积物的沉积阶段和后期的区域变质作用阶段,变质成矿流体发生了不混溶现象,对成矿元素的富集起到一定的促进作用。     

内蒙古合教BIF型铁矿的形成时代、地球化学特征及地质意义

内蒙古合教铁矿位于华北克拉通西部陆块北缘阴山地块,是固阳绿岩带内的一例具有中型规模的BIF型铁矿床.本文对矿区斜长角闪岩、铁矿石开展了年代学和岩石地球化学研究.对斜长角闪岩夹层进行LA-ICP-MS锆石U-Pb定年,锆石普遍发育振荡环带,Th/U比值均大于0.1（0.27~1.00）,得到上交点年龄为2 549±29 Ma（MSWD=0.51）,可大致代表合教BIF铁矿的形成时代,该时期是华北克拉通早寒武纪构造-变质-热事件和BIF（banded iron formation）形成最为强烈的时期（2.52~2.60 Ga）.斜长角闪岩原岩可能为玄武岩,表明合教铁矿为与火山活动关系密切的Algoma型BIF.斜长角闪岩稀土元素球粒陨石标准化配分曲线近于平坦,与E-MORB和弧后盆地玄武岩（BABB）曲线相似,原始地幔标准化蛛网图与BABB曲线相似,均存在Rb、Ba、Sr、K等大离子亲石元素的富集和Nb、Ta、U、Th等高场强元素的亏损,显示了岛弧岩浆岩的特征,结合前人提出的岛弧叠加地幔柱构造模式,认为合教斜长角闪岩原岩形成于弧后盆地构造环境,并有地幔柱的叠加作用,代表了合教BIF沉积时的构造环境.铁矿石LREE亏损,HREE富集[（La/Yb）_PAAS=0.29~0.50],具有轻微的La正异常（La/La*=1.00~1.13）,不明显的Ce负异常（Ce/Ce*=0.90~0.95）,明显的Eu正异常（Eu/Eu*=1.54~2.27）和较明显的Y正异常（Y/Y*=1.07~1.42）.铁矿石的稀土配分曲线与固阳绿岩带科马提岩和海底热液海水混合物均极为相似,表明合教BIF的形成与海底热液活动有关,认为合教BIF型铁矿的Fe主要由海底高温热液淋滤科马提岩提供.      

中国磁性铁矿石全铁品位和磁性铁品位关系及其意义

中国铁矿以可磁选的低品位磁性铁矿石为主,但是圈定铁矿体多以全铁品位为依据。文章整理了矿产资源储量数据库中磁性铁矿石的全铁品位及其对应磁性铁品位数据,筛选出493组数据,建立了沉积变质型、岩浆型、火山岩型、矽卡岩-热液型铁矿床磁性铁矿石的全铁（TFe）品位与磁性铁（mFe）品位关系式,全部493组数据为mFe(%)=0.9077TFe(%)-3.1442,沉积变质型铁矿为mFe(%)=0.8605TFe(%)-1.8275,火山岩型铁矿为mFe(%)=0.6669TFe(%)+2.6842,矽卡岩-热液型铁矿为mFe(%)=0.9320TFe(%)-3.2442,岩浆型铁矿为mFe(%)=0.8799TFe(%)-3.0174。假定铁矿石的全铁品位为20%和25%时,根据这些关系式估算的磁性铁品位与地质行业规范的边界品位（w(TFe)≥20%,w(mFe)≥15%）和最低工业品位（w(TFe)≥25%,w(mFe)≥20%）十分一致。磁性铁品位的估算,对评价铁矿资源的可利用性、进行国际对比和研究保障程度具有重要参考价值。     

弓长岭铁矿蚀变岩及富矿成因

弓长岭铁矿床是鞍山本溪地区最典型的BIF型铁矿床之一,而且是该地区最大的富铁矿产区。从野外产出关系来看,弓长岭矿区的富铁矿与蚀变岩密切相关,蚀变岩与富铁矿基本上是形影相随。蚀变岩具有分带性,由富铁矿向外依次为镁铁闪石岩石榴石岩绿泥石岩弱蚀变斜长角闪岩斜长角闪岩。弱蚀变岩保留了蚀变原岩的岩貌特征,矿物的蚀变并不完全,可见残余的原生矿物。强蚀变岩的蚀变较彻底,基本无原生矿物残留。将蚀变岩与斜长角闪岩、磁铁石英岩的地球化学特征进行对比可以发现弱蚀变岩、石榴石岩、绿泥石岩与斜长角闪岩的痕量元素特征基本一致,而镁铁闪石岩的痕量元素特征更接近磁铁石英岩。再结合镜下特征、野外接触关系、主量元素特征等证据,认为除了镁铁闪石岩是由磁铁石英岩蚀变形成,其余蚀变岩都是由斜长角闪岩蚀变形成。根据各类蚀变岩中主要矿物的(Fe+Mg)/Si值以及蚀变岩的SiO2和Fe2OT3含量变化规律可以发现,在蚀变岩和富矿形成过程中发生了Mg、Fe以及Si的迁移。对本次取样的样品进行原岩恢复和构造环境判别投图,投图结果表明,绿泥石岩和弱蚀变岩的最初原岩都是形成于弧后盆地的玄武岩。     

Water determination in iron oxyhydroxides and iron ores by Karl Fischer titration

Protohematite (Fe_2?x/3(OH) _x O_3?x 1 ≤ x < 0.5) and hydrohematite (Fe_2?x/3(OH) _x O_3?x 0.5 ≤ x < 0) are iron-defective phases containing hydroxyl groups in their structures. These species were described in prior studies mainly with the aid of X-ray diffraction and Infrared spectroscopy. The existence of these phases in soils might have influence in redox processes, and they were considered as a possible water reservoir in Martian soils. In this study, we have used for the first time the Karl Fischer titration method to determine the amount of water released after heating several synthetic samples of goethite, hematite and natural iron ores at 105, 400, 600 and 900 °C. It was found that heating at 105 °C did not remove all moisture from the samples, and higher temperatures were necessary to completely remove all the absorbed water. The water contents determined at 400, 600 and 900 °C were found to be the same within the experimental errors, suggesting the inexistence of both protohematite and hydrohematite in the investigated samples. Therefore, the above-mentioned effects of these phases in soils might have to be reevaluated.     

Neoproterozoic banded iron formations

Two epochs of the formation of ferruginous quartzites—Archean-Paleoproterozoic (3.2–1.8 Ga) and Neoproterozoic (0.85–0.7 Ga)—are distinguished in the Precambrian. They are incommensurable in scale: the Paleoproterozoic Kursk Group of the Kursk Magnetic Anomaly (KMA) extends over 1500 km, whereas the extension of Neoproterozoic banded iron formations (BIF) beds does not exceed a few tens of kilometers. Their thickness is up to 200 m and not more than 10 m, respectively. The oldest BIFs are located in old platforms, whereas Neoproterozoic BIFs are mainly confined to Phanerozoic orogenic (mobile) zones. Neoproterozoic BIFs universally associate with glacial deposits and their beds include glacial dropstones. In places, they underlie tillites of the Laplandian (Marinoan) glaciation (635 Ma), but they are more often sandwiched between glaciogenic sequences of the Laplandian and preceding Sturtian or Rapitan glaciation (730–750 Ma). Neoproterozoic BIFs are rather diverse in terms of lithology due to variation in the grade of metamorphism from place to place from low grades of the greenschist facies up to the granulite facies. Correspondingly, the ore component is mainly represented by hematite or magnetite. The REE distribution and (Co + Ni + Cu) index suggest an influence of hydrothermal sources of Fe, although it was subordinate to the continental washout. Iron was accumulated in seawater during glaciations, whereas iron mineralization took place at the earliest stages of postglacial transgressions.     

Ferric iron in tourmaline

Red Fe³⁺-rich and black Fe³⁺, Fe²⁺-rich tourmalines have been studied by optical and Mössbauer spectroscopies to determine the optical characteristics of Fe³⁺ in tourmaline. Prominent optical absorption features at 485 and 540 nm are assigned to transitions of multiple exchange-coupled Fe³⁺ pairs in several site combinations. These transitions are more intense than those of isolated Fe³⁺ and are polarized along the vector between the interacting ions, thus permitting site assignments. The 485 nm band occurs at an unusually low energy for Fe³⁺ in silicate minerals. Similar behavior has been observed in the spectrum of coalingite, Mg₁₀Fe ₂ ³⁺ (OH)₂₄CO₃·2H₂O, in which Fe³⁺ occurs in related pairs in edge-shared sheets. These lower energies are proposed to result from magnetic exchange in edge-shared geometries. Antiferromagnetic exchange has been confirmed by a variable temperature magnetic susceptibility study of a Kenyan dravite with 3.36 wt percent Fe. The Mössbauer spectrum of this sample is unusual in that it shows a pronounced decrease in width of component peaks from 298 K to 5 K.     

Closed system Fischer-Tropsch synthesis over meteoritic iron,iron ore and nickel-iron alloy

Meteoritic iron, iron ore and nickel-iron alloy (either alone or in some cases mixed with alumina, carbonaceous chondrite, potassium carbonate or sodium carbonate) were used to catalyze the reaction of deuterium and carbon monoxide in a closed reaction vessel. The mole ratio of deuterium to carbon monoxide ranged from 1/2:1 to 10:1, the reaction temperature from 195 to 370°C, and the reaction time from 6 to 480 hr. Analysis of the reaction products showed that normal alkanes and alkenes (C₁₁-C₂₅), their monomethyl substituted isomers and aromatic hydrocarbons (e.g. naphthalene, acenaphthene, fluorene, phenanthrene and the methyl derivatives of these hydrocarbons) were synthesized. In addition to the aforementioned hydrocarbons, one reaction product was shown to contain perdeutero normal fatty acids (10:0–16:0).     

An iron isotope signature related to electron transfer between aqueous ferrous iron and goethite

We measured the Fe isotope fractionation during the reactions of Fe(II) with goethite in the presence and absence of a strong Fe(III) chelator (desferrioxamine mesylate, DFAM). All experiments were completed in an O₂-free glove box. The concentrations of aqueous Fe(II) ([Fe(II)_aq]) decreased below the initial total dissolved Fe concentrations ([Fe(II)_total], 2.15 mM) due to fast adsorption within 0.2 day. The concentration of adsorbed Fe(II) ([Fe(II)_ads]) was determined as the difference between [Fe(II)_aq] and the concentration of extracted Fe(II) in 0.5 M HCl ([Fe(II)_extr]) (i.e., [Fe(II)_ads] = [Fe(II)_extr] − [Fe(II)_aq]). [Fe(II)_ads] also decreased with time in experiments with and without DFAM, documenting that fast adsorption was accompanied by a second, slower reaction. Interestingly, [Fe(II)_extr] was always smaller than [Fe(II)_total], indicating that some Fe(II) was sequestered into a pool that is not HCl-extractable. The difference was attributed to Fe(II) incorporated into goethite structure (i.e., [Fe(II)_inc] = [Fe(II)_total] −[Fe(II)_extr]). More Fe(II) was incorporated in the presence of DFAM than in its absence at all time steps. Regardless of the presence of DFAM, both aqueous and extracted Fe(II) (δ^56/54Fe(II)_aq and δ^56/54Fe(II)_extr) became isotopically lighter than or similar to goethite (− 0.27‰) at day 7, implying that the isotope exchange occurred between bulk goethite and aqueous Fe. Consistently, the mass balance indicated that the incorporated Fe is isotopically heavier than extracted Fe. These observations suggested that (i) co-adsorption of Fe(II) with DFAM resulted in more pervasive electron transfer, (ii) the electron transfer from heavy Fe(II) in the adsorbed Fe(II) to light Fe(III) in goethite results in the fixation of heavy adsorbed Fe(III) on the surface and accumulation of Fe(II) within the goethite, and (iii) desorption of the reduced, light Fe from goethite does not necessarily occur at the same surface sites where adsorption occurred.     

新疆塔县乔普卡铁矿和山东莱州土山铁矿特征对比

虽然乔普卡铁矿和土山铁矿在地理位置上相隔甚远,但是二者在赋矿层位、磁异常特征、矿体及围岩特征、矿石结构构造、矿物成分和矿石类型以及矿床成因等诸多方面存在着较大的相似性,进一步研究对比二者的共同和异同点,对于寻找此类矿床有一定的指导作用。本文主要在乔普卡铁矿和土山铁矿详查工作和参考前人工作研究的基础上,对比分析了两个铁矿的异同点,从而总结出相邻区域里寻找此类矿床的几个注意点。