由MgMn_2O_4制备新型离子筛吸附剂及其对锂的吸附性质

从Mg、Mn混合溶液制备了镁锰氧化物MgMn_2O_4,并由此制得新型离子筛氧化锰HMnO(Mg)。它在碱金属及碱土金属离子中对Li~+显示了很高的选择性,pH8时分配系数Kd值顺序为Li>>Ca>Mg>K>Na,可以从实际卤水中将Li~+选择性吸附,吸附容量达20.4mg/g,用稀HCI溶液易于将吸附的Lj~+洗脱并使吸附剂再生。经用卤水和HCI五次吸附——洗脱循环,Li~+吸附容量没有降低,洗脱率总是大于90％。     

镁离子电池正极材料MgNi0.4Mn1.6O4的合成及温度的影响

采用溶胶-凝胶法合成了镁离子电池MgNi0.4Mn1.6O4正极材料,并考查了合成温度对产物结构及电化学性能的影响。利用热重-差热重量分析法(TG-DTG)、X射线衍射法(XRD)、扫描电镜(SEM)等对样品进行了表征和分析。结果表明当煅烧温度为900℃时,所得样品为纯相的MgNi0.4Mn1.6O4样品。在0.3～2.1 V电压范围内,以0.025 mA为充放电电流时,首次放电比容量为150.6 mAh/g。     

球形MnO2·0.5H2O提锂性能及其机理研究(英文)

考察了形貌对尖晶石型锂离子筛吸附剂MnO₂·0.5H₂O吸附性能的影响。实验证明,反应物Mn₂O₃的形貌在很大程度上决定了前驱体及其吸附剂的形貌。采用XRD、SEM、TEM、FT-IR、XPS和N₂吸附—解吸等温线等对样品进行了表征。表征和吸附实验结果表明,与立方形锂离子筛相比,球形锂离子筛具有较高的吸附容量(42.46 mg/g),同时对溶液中的Li+具有较高的选择性。表面脱质子和离子交换过程的共同作用增强了离子筛型吸附剂的提锂Li⁺性能。此外,本文对Li_1.6Mn_1.6O₄与MnO₂·0.5H₂O的吸附—解吸机理进行了解释。     

Fe3O4/Mg(OH)2复合材料的制备及对铅离子的移除应用

通过种子沉积法制备出Fe_3O_4/Mg(OH)_2复合材料并进行了XRD、SEM、TEM、SAED测试分析。将该复合材料对水溶液中Pb~(2+)进行移除应用实验,接触时间为240 min时达到平衡。平衡时,水溶液中的Pb~(2+)超过90%被移除,移除量为950.8 mg/g。通过动力学研究发现,移除过程符合准二级动力学模型,这意味着移除过程中可能为化学吸附及沉淀过程。     

青海可可西里东北部多秀湖和盐湖水化学特征研究

2016年3月系统采集了青海可可西里东北部多秀湖和盐湖的湖水及其入湖冰川融水。研究发现,两个湖泊湖水中离子含量均较高,主要阳离子含量顺序均为Na~+Mg~(2+)K~+Ca~(2+),主要阴离子含量顺序均为Cl~-SO_4~(2-)HCO_3~-CO_3~(2-);而入湖冰川融水的离子含量非常低。根据库尔纳可夫—瓦良什科水化学分类标准,多秀湖湖水属于硫酸盐型—硫酸镁亚型,盐湖湖水属于硫酸盐型—硫酸钠亚型。多秀湖和盐湖湖水Li—Mg—B的相关性均为正相关,说明两个湖泊中这3种元素的物质来源、搬运条件及富集环境具有很强的相似性。由于气候变暖导致大量矿化度低的冰川融水注入盐湖,矿化度较低的卓乃湖和库赛湖决堤湖水泄入盐湖,使得盐湖的面积较1997年扩大了5倍,湖水的矿化度降低了约10倍,而多秀湖近些年湖水矿化度变化较小。多秀湖湖水矿化度以及Li~+、Mg~(2+)和B_2O_3含量均较高,具有较好的资源潜在利用价值。     

以PAC为原料合成锂吸附剂的工艺研究

研究了聚合氯化铝(PAC)为原料合成锂吸附剂的基本工艺路线,并探究了加料方式、反应物配比、反应温度、反应时间和加料速度等对所合成吸附剂吸附量的影响,研究结果表明配比是影响吸附剂吸附量的最主要因素,得到了最佳合成条件,在此条件下所合成吸附剂对锂离子的吸附容量为6.1 mg/g。推断吸附剂的主要成分为晶态或非晶态的LiCl·2Al(OH)_3·nH_2O,同时含有Al(OH)_3、(CaO)_3Al_2O_3·6H_2O及LiCl·H_2O等成分。从吸附结果来看,结晶度较差的片状LiCl·2Al(OH)_3·nH_2O和非晶态的Al(OH)_3为主成分的吸附剂吸附性能最好。     

抗性真菌对Pb2+、Zn2+和Cu2+的吸附特性研究

从铜陵市某矿区土壤中筛选出1株对重金属Pb2+、Zn2+和Cu2+具有抗性的真菌,命名为TL-3。以TL-3为实验菌株,在不同pH值、不同金属离子初始浓度、不同菌体量以及不同吸附时间条件下对Pb2+、Zn2+和Cu2+进行吸附实验,研究其吸附特性与对不同金属离子的吸附能力。结果表明,TL-3对Pb2+、Zn2+和Cu2+的最佳pH值为5.0。在最佳条件下,吸附量在Pb2+,Zn2+和Cu2+的初始浓度分别为200mg/L、300mg/L和200mg/L达到最大,分别为20.61mg/g,23.17mg/g和17.46mg/g。TL-3对三种重金属的吸附均在20h达到吸附平衡。     

利用普鲁士蓝/活性炭复合材料回收提钾后的盐湖卤水中铯

以亚铁氰化钾为单源前驱体,以活性炭为载体,采用超声辅助均匀沉淀法,制备了普鲁士蓝/活性炭复合材料(PB/AC)。通过场发射扫描电子显微镜、X-射线衍射、X-射线光电子能谱和傅立叶变换红外光谱技术,对PB/AC的形貌、结构和组成进行了表征。结果表明:立方体结构的PB微晶均匀地分布在活性炭表面。研究考察了PB/AC对水溶液中铯离子(Cs~+)的吸附和脱附性能。在pH=7、45℃和180 min条件下,PB/AC对Cs~+的最大吸附量为49.17 mg/g;在pH=2、45℃和240 min条件下,Cs~+的脱附率可达88.5%。     

Al掺杂对尖晶石型LiMn2O4结构及循环性能的影响

用柠檬酸作为螯合物的载体,采用溶胶-凝胶法合成了Al3+掺杂的锂离子电池正极材料LiAlxMn2-xO4,并用XRD、SEM等多种测试手段研究了不同掺杂铝量对粉体形貌、晶体结构的影响。结果表明,800℃烧结可获得单一尖晶石结构的物相。随着Al3+掺入量的增加,LiAlxMn2-xO4的晶格常数变小,晶格更趋于完整,有利于抑制因锂的反复脱嵌而造成结构的破坏。实验表明,当掺Al量为0.05时,首次放电容量为103.8 mAh/g,25次循环后容量还有100.6 mAh/g,容量衰减仅为3.08%。该正极材料具备高的容量和优异的循环性能。     

补水背景下大盐滩矿区潜卤水水化学特征

为探究补水背景下大盐滩矿区潜卤水水化学组分的变化规律,采用水化学分析测试方法,对2015年5月和7月分别就矿区33口长期观测孔内潜卤水中的Ca~(2+)、K~+、Na~+、Mg~(2+)、HCO_3~-、SO_4~(2-)、Cl~-的含量进行测定,分析矿区潜卤水中Ca~(2+)、K~+、Na~+、Mg~(2+)、SO_4~(2-)、Cl~-的变化趋势,并查明其分布特征。结果表明:补水背景下,大盐滩矿区潜水含水层中的潜卤水水化学组分在时间和空间上存在着明显的变化。在时间上,5~7月时间段内,K~+,Na~+、Mg~(2+)、SO_4~(2-)的浓度升高,且Na~+浓度变化幅度较大;Ca~(2+)、Cl~-浓度降低。在空间上,矿区中部和东南部,晶间潜卤水中的K~+、Mg~(2+)、SO_4~(2-)浓度较高;矿区北部晶间潜卤水中的K~+、Mg~(2+)、SO_4~(2-)的浓度则相对较低。补水可以适当地增大开采区域潜卤水中K~+的浓度,提升卤水的质量。     

青藏高原高硼卤水的水化学特征及其成因

本文就青藏高原高硼卤水的分布、水化学特征、硼与共生元素的相关性及硼矿沉积的某些规律作了阐述,进而探讨了高硼卤水的成因。     

纳滤法用于铝锂分离的初步研究

本文探讨了纳滤分离Al³⁺和Li⁺的可行性,研究了含盐量和铝锂比对分离效率的影响,提出了从锂云母浸出液中分离回收锂的新方法。实验结果表明,纳滤膜对Al³⁺和Li⁺的截留率随含盐量的升高而降低,其中Li⁺始终呈现负浓度梯度扩散的趋势,而Al³⁺的截留率始终稳定在99%以上。当含盐量为45 g/L时,铝锂分离因子最高可达248.33,膜面相应Zeta电位的绝对值达到最大。随着溶液中铝锂比的变化,Al³⁺和Li⁺的截留率分别在不同铝锂比的条件下出现拐点,溶液的pH呈现先下降后上升最后下降的复杂趋势。本实验研究发现,DK膜能够在酸性环境下实现高效的铝锂分离和锂的浓缩,从而为锂云母浸出液中锂的提取提供新的思路。     

新型复合生物质锂吸附剂的制备及吸附性能研究

以KMnO₄、苯胺、LiOH和生物质碳气凝胶(BCA)为原料,通过水热沉积法得到了锰酸锂(LMO)负载的生物质碳气凝胶(BCA@LMO),并用HCl酸洗后得到了BCA@HMO复合锂吸附剂。利用IR、XRD、XPS、SEM、EDS、Mapping、BET等手段对其结构进行了表征。考察了pH值、离子强度、初始浓度、温度和吸附时间对锂吸附的影响。结果表明,复合吸附剂为介孔结构,其孔道内和表面具有丰富的锰酸锂颗粒,Li⁺的最大平衡吸附量在pH=12时为4.07 mmol·g-1,吸附过程符合Langmuir等温线和准二阶动力学模型,升高温度和碱性环境利于Li⁺的吸附。吸附机理为H⁺与Li⁺的离子交换。复合吸附剂较好地改善了锰系锂吸附剂固液分离困难的问题,该吸附剂在实际南翼山盐田和东台吉乃尔盐田卤水(2.92 mmol·g-1)中具有良好的吸附性能。因此,该吸附剂在卤水锂的分离中具有良好的应用价值和潜力。     

Li+,Na+,K+/Cl-,SO2-4-H2O五元体系25 ℃相图及其应用

Li⁺,Na⁺,K⁺/Cl-,SO2-₄-H₂O五元体系相图对于硫酸钠亚型富锂卤水分离提取锂盐、锂辉石加工利用和锂盐产品的开发利用工艺制定都有指导作用。20世纪50年代曾有人研究过这一体系25 ℃时的相图,限于当时的科研水平,液相组成确定不准确,对平衡固相的判断,后来诸多研究结果证明也有错误。50多年来再没有人研究这一五元体系相图。利用我们提出的Li⁺,Na⁺,K⁺/Cl^-,SO^2-₄-H₂O六元体系热力学模型,对该五元体系的平衡溶液组成和正确的平衡固相进行理论预测,给出了该体系的完整相图。结合硫酸锂混盐分离、加工实例阐述了该五元体系相图的应用。     

Hydrochemical Characteristics and Sodification of Groundwater in the Shirin Sou, Hamedan, Western Iran

Salinity and sodicity of groundwater are the principal water quality concerns in irrigated areas of arid and semi-arid regions. The hydrochemical characteristics and sodicity of groundwater in the Shirin Sou area, western Iran were investigated in this study by chemical analyses of groundwater samples from 49 wells. Chemical analysis of the groundwater showed that the mean concentration of the cations was in the order: Na⁺ > Ca²⁺ > Mg²⁺ > K⁺, while that for anions was SO₃ ²⁻ > Cl⁻ > HCO₃ ⁻ > NO₃ ⁻. The most prevalent water type is Na–SO₄ followed by water types Na–Cl and Ca–SO₄. The chemical evolution of groundwater is primarily controlled by water–rock interactions: mainly weathering of aluminosilicates, dissolution of sulfate minerals, and cation exchange reactions. Sulfate dissolution and pyrite weathering may both contribute to the SO₄ ²⁻ load of the groundwater. High Na⁺ concentrations in groundwater participate in ion-exchange processes, resulting in the displacement of base cations into solution and raised concentrations in groundwater. The principal component analysis (PCA) performed on groundwater identified three principal components controlling variability of groundwater chemistry. Electrical conductivity, Ca²⁺, Mg²⁺, Na⁺, SO₄ ²⁻, and Cl⁻ content were associated in the same component (PC1) (salinity), most likely linked to anthropogenic activities.     

LiM_xMn_(2-x)O_4(M=Cr、Al)尖晶石相阴极材料研究

用溶胶 -凝胶法制备了 L i Mx Mn2 - x O4( M=Cr、Al;x≤ 0 .2 )尖晶石相锂离子电池阴极材料。SEM表面观测显示材料的晶形好 ,粒度均匀 ,粒径小于 0 .5微米。电化学测试表明 ,低水平量 ( 0 .0 2≤ x≤ 0 .0 5 )的 Cr、Al掺杂材料初始容量稍有降低 ,但却较大地改善了循环性能。在 L i Mx Mn2 - x O4中 ,掺 Al降低了 L i+、Mn3+占位的无序度 ;Cr3+和 Al3+取代了其中的部分 Mn3+ ,占据八面体位 ( 16 d) ,抑制了 Jahn-Teller效应 ,增强了尖晶石骨架的稳定性 ,提高了其电化学性能。在 3.0～ 4.3V的充放电过程中 ,材料中的 Cr、Al都保持 +3价不变 ,不发生氧化还原     

Hydrochemical regime and its mechanism in Yamzhog Yumco Basin,South Tibet

The hydrochemistry of alpine lakes reflects water characteristic and its response to climatic change. Over 300 water samples had been collected from 52 sites of 5 lakes and 7 inflowing rivers in the Yamzhog Yumco Basin, South Tibet, during 2009–2014, basing which the hydrochemical regime and its mechanism were analyzed along with the adoption of hydrological investigations in 1979 and 1984 as well. Results revealed that the waters were hard with weak alkalinity for the Yamzhog Yumco Basin. Most of them were fresh, and the rest were slightly saline. The hydrochemical types of 5 lakes (i.e., Lake Yamzhog Yum Co, Puma Yum Co, Bajiu Co, Kongmu Co, and Chen Co) were SO₄ ^2––HCO₃ ^––Mg²⁺–Na⁺, HCO₃ ^––SO₄ ^2––Mg²⁺–Ca²⁺, SO₄ ^2––Mg²⁺–Na⁺, SO₄ ^2––HCO₃ ^––Ca²⁺, and SO₄ ^2––Na⁺–Mg²⁺–Ca²⁺, respectively. As for rivers, HCO₃ ^– and SO₄ ^2– were the major anions, and Ca²⁺ was the dominant cation. Lake Yamzhog Yum Co, the largest lake in the basin, exhibited remarkable spatial variations in hydrochemistry at its surface but irregular changes with depth. The weathering of evaporates and carbonates, together with evaporation and crystallization, were the major mechanisms controlling the hydrochemistry of waters in the Yamzhog Yumco Basin. Global warming also had significant impacts on hydrochemical variations.     

Geochemistry of waters and brines from the Salinas Grandes basin,Córdoba,Argentina. I. Geomorphology and hydrochemical characteristics

This paper reports on hydrochemical features of diluted waters in the source areas and the brine end-members dominant in the playa of the Salinas Grandes Basin, Córdoba, Argentina. Special emphasis was placed on the study of the relationship between geomorphology and the resulting hydrochemical fractionation. Inflow is from springs and mountain streams which disappear before reaching the saline complex. The playa and intermittent saline lakes are mainly fed by groundwater flow and a few moderately saline and perennial springs. Conversely, ephemeral lakes are fed by atmospheric precipitation and groundwater, whereas small ponds are only fed by atmospheric precipitation. The absence of a clear linkage between geomorphological units and water types was evident in the source areas. Up to four types of water were recognized in a given geomorphological unit. From the sandflat downward towards the playa, the correspondence between geomorphological units and water types was clear, coinciding with a decreased hydrochemical heterogeneity. In this subenvironment, I have recognized two dominant types of water (SO ₄ ^2– –Cl^––HCO ₃ ^– –Na⁺ and Cl^––SO ₄ ^2– –HCO ₃ ^– –Na⁺), which can be considered the original members of the neutral brine in the playa (Cl^––SO ₄ ^2– –Na⁺ where Ca²⁺+Mg²⁺ do not surpass 5 meq per cent), and an intermediate type in the mudflat (Cl^––SO ₄ ^2– –Na⁺ where the contribution of Ca²⁺+Mg²⁺ reaches up to 15 meq per cent). It seems evident that in the zone between the source areas and the sandflat, hydrochemistry is governed by chemical weathering. In stream floodplains and in the distal alluvial plain, close to the saline complex, the increase in water types as well as the increase of HCO ₃ ^– with respect to SO ₄ ^2– , were explained by the mixture of aquifers controlled by the Salinas Grandes-Salinas de Ambargasta fracture. In the saline complex, the more concentrated end-members are the result of evaporation of the two more frequent water-types in the sandflat subenvironment, and salt dissolution of ancient evaporite deposit.     

柴达木盆地中西部背斜构造深层卤水水化学特征与成因

柴达木盆地西部背斜构造深层卤水资源勘查和评价成果显示,第三系背斜构造赋存深层卤水,具有良好的资源成矿条件,且潜力大。采集柴达木盆地中西部(一里坪拗陷和三湖拗陷)9处背斜构造深层卤水,分析了其水化学特征与成因。结果表明,深层卤水矿化度一般低于150 g/L,水化学类型均为氯化物型;K⁺、Na⁺、Mg²⁺含量较低,不具找矿价值;而B₂O₃、Li⁺含量普遍高于评价指标,Br-、I-含量普遍高于综合评价指标,为主要成矿元素;卤水的元素特征系数和分布规律及微量离子组成揭示,深层卤水是大气降水溶滤盆地周缘岩浆岩和火山岩及火山热泉的补给后,汇入古近纪—新近纪湖盆经蒸发浓缩封存在地层中的沉积卤水。