Rare-earth element geochemistry reveals the provenance of sediments on the southwestern margin of the Challenger Deep

The hadal zone represents one of the last great frontiers in modern marine science,and deciphering the provenance of sediment that is supplied to these trench settings remains a largely unanswered question.Here,we examine the mineralogical and geochemical composition of a sediment core(core CD-1)that was recovered from the southwestern margin of the Challenger Deep within the Mariana Trench.Major element abundances and rare-earth element patterns from these sediments require inputs from both terrigenous dust and locally sourced volcanic debris.We exploit a two-endmember mixing model to demonstrate that locally sourced volcanic material dominates the sediment supply to the Challenger Deep(averaging^72%).The remainder,however,is supplied by aeolian dust(averaging^28%),which is consistent with adjacent studies that utilized Sr-Nd isotopic data.Building on a growing database,we strengthen our understanding of Asian aeolian dust input into the northwestern Pacific,which ultimately improves our appreciation of sedimentation in,and around,the hadal zone.

Geochemical characteristics and their significances of rare-earth elements in deep-water well core at the Lingnan Low Uplift Area of the Qiongdongnan Basin

A geochemical analysis of rare-earth elements （REEs） in 97 samples collected from the core of deep-water Well LS-A located at the Lingnan Low Uplift Area of the Qiongdongnan Basin is conducted, with the pur-pose of revealing the changes of sedimentary source and environment in the study region since Oligocene and evaluating the response of geochemical characteristics of REEs to the tectonic evolution. In the core samples, both∑REE and∑LREE （LREE is short for light-group REEs） fluctuate in a relatively wide range, while∑HREE （HREE is short for heavy-group REEs） maintains a relatively stable level. With the stratigraphic chronology becoming newer, both∑REE and∑LREE show a gradually rising trend overall. The∑REE of the core is relatively high from the bottom of Yacheng Formation （at a well depth of 4 207 m） to the top of Ledong Formation, and the REEs show partitioning characteristics of the enrichment of LREE, the stable content of HREE, and the negative anomaly of Eu to varying degrees. Overall the geochemical characteristics of REEs are relatively approximate to those of China＇s neritic sediments and loess, with significant ＂continental ori-entation＂. The∑REE of the core is relatively low in the lower part of Yacheng Formation （at a well depth of 4 207-4 330 m）, as shown by the REEs partitioning characteristics of the depletion of LREE, the relative enrich-ment of HREE, and the positive anomaly of Eu; the geochemical characteristics of REEs are approximate to those of oceanic crust and basalt overall, indicating that the provenance is primarily composed of volcanic eruption matters. As shown by the analyses based on sequence stratigraphy and mineralogy, the provenance in study region in the early Oligocene mainly resulted from the volcanic materials of the peripheral uplift ar-eas; the continental margin materials from the north contributed only insignificantly; the provenance devel-oped to a certain extent in the late Oligocene. Since the Miocene, the provenance has ceaselessly expanded from proximal to distal realm, embodying a characteristic of multi-source sedimentation. In the core strata with 31.5, 28.4, 25.5, 23, and 16 Ma from today, the geochemical parameters of REEs and Th/Sc ratio have significant saltation, embodying the tectonic movement events in the evolution of the Qiongdongnan Basin. In the tectonic evolution history of the South China Sea, the South China Sea Movement （34-25 Ma BP, early expansion of the South China Sea）, Baiyun Movement （23 Ma BP）, late expansion movement （23.5-16.5 Ma BP）, expansion-settlement transition, and other important events are all clearly recorded by the geochemi-cal characteristics of REEs in the core.

Rare-earth and trace elements and hydrogen and oxygen isotopic compositions of Cretaceous kaolinitic sediments from the Lower Benue Trough, Nigeria: provenance and paleoclimatic significance

This study evaluated the Cretaceous(Campanian–Maastrichtian) kaolinitic sediments of the Ajali/Mamu and Enugu/Nkporo Formations from the Lower Benue Trough of Nigeria. A combined method of inductively coupled plasma–mass spectrometry and isotope ratio mass spectrometry was used to investigate trace and rareearth element geochemistry and hydrogen and oxygen isotopic compositions. These data were then used to infer the sediments' provenance and paleoclimatic conditions during their deposition. The sediments contained low concentrations of most trace elements, with the exceptions of Zr(651–1352 ppm), Ba(56–157 ppm), V(38–90 ppm),and Sr(15.1–59.6 ppm). Average values of Co and Ni were1.5 and 0.7 ppm, respectively. Trace and rare earth element values were lower than corresponding values for upper continental crust and Post-Archean Australian Shale, with the exception of Zr. The samples showed only slight light rare-earth enrichment and nearly flat heavy rare-earth depletion patterns, with negative Eu and Tm anomalies,typical of felsic sources. Geochemical parameters such as La/Sc, Th/Sc, and Th/Co ratios support that the kaolinitic sediments were derived from a felsic rock source, likely deposited in an oxic environment.^(18 )O values ranged from+ 15.4 to + 21.2% for the investigated samples, consistent with a residual material derived from chemicalweathering of felsic rock and redeposited in a sedimentary basin(typical values of + 19 to + 21.2%). While in the basin, the sediments experienced extended interactions with meteoric water enriched in d D and d16 O. However,the variation in d D and d16 O values for the investigated samples is attributed to the high temperature of formation(54–91 °C). The d D and d^(18 )O values suggest that the sediments, although obtained from different localities within the Lower Benue Trough, formed under similar hot,tropical climatic conditions.

Mechanism of interaction relation between the rare-earth element Ce and impurity elements Pb and Bi in Ag-based filler metal

The mechanism of interaction relation between the rare-earth element Ce and elements Pb and Bi in Ag-based filler metal has been studied. The results show that the compounds CePb and CeBi with high melting point can be easily produced between these three elements in the filler metal, which greatly limited the formation of the isolated phase Pb or Bi and also eliminated the bad effect of impurity elements Pb and Bi on the spreading property of Ag-based filler metal. The metallurgical and quantum-mechanical bond formation analysis show that a strong chemical affinity was existed between the rare-earth element Ce and impurity elements Pb and Bi, which was proved by the XRD analysis results.

Effects of rare-earth elements on the glass-forming ability and mechanical properties of Cu_(46)Zr_(47-x)Al_7M_x(M = Ce,Pr,Tb,and Gd) bulk metallic glasses

Cu46Zr47-xA17Mx （M = Ce, Pr, Tb, and Gd） bulk metallic glassy （BMG） alloys were prepared by copper-mold vacuum suction casting. The effects of rare-earth elements on the glass-forming ability （GFA）, thermal stability, and mechanical properties of Cu46Zr47-xA17Mx were investigated. The GFA of Cu46Zr47-xA17Mx （M = Ce, Pr） alloys is dependent on the content of Ce and Pr, and the optimal content is 4 at.%. Cu46Zr47-xA17Thx（X = 2, 4, and 5） amorphous alloys with a diameter of 5 mm can be prepared. The GFA of Cu46Zr47-xA17Gdx（x = 2, 4, and 5） increases with increasing Gd. Tx and Tp of all decrease. Tg is dependent on the rare-earth element and its content. ATx for most of these alloys decreases except the Cu46Zra2Al7Gd5 alloy. The activation energies △Eg, △Ex, and △Ep for the Cu46Zr42A17Gd5 BMG alloy with Kissinger equations are 340.7, 211.3, and 211.3 kJ/mol, respectively. These values with Ozawa equations are 334.8, 210.3, and 210.3 kJ/mol, respec- tively. The Cu46Zr45Al7Tb2 alloy presents the highest microhardness, Hv 590, while the Cu46Zr43A17Pr4 alloy presents the least, Hv 479. The compressive strength （at.f.） of the Cu46Zra3A17Gd4 BMG alloy is higher than that of the Cu46Zr43Al7Tb4 BMG alloy.

INFLUENCE OF RARE-EARTH ELEMENTS ON THERMAL STABILITY OF PdSi_(16.5)GLASS

The influence of rare-earth elements,La,Ce,Pr,Nd,Sm,Eu,Gd,Dy,Ho,Er and Yb on the thermal stability of PdSi_(16.5) glass was studied systematically by means of DSC.All rare-earth elements,especially heavy ones,increase obviously the thermal stability parameters,including T_θ(T_g ,T_x ,T_g),T_(rg) and ΔE etc.The crystallization temperatures T_(p1) and T_(p2) increase linearly with the lanthanide constriction increasing,but Eu shows an anomalous influence:Pd-Si-Eu metallic glass possesses the highest thermal stability and the lowest concentration limit of glass forming among Pd-Si-R glasses.

Influence of Rare-Earth Elements on ElectricalProperties of Pd

The influence of RE (RE = La, Ce. Pr. Nd, Sm, Eu, Gd. Tb. Dy, Er, Yb) additives with dilute concentrations on the electrical properties of Pd has been studied. All RE elements increase the specific resistivity (ρ) and decrease the resistance temperature coefficient (α) of Pd. and (ρ.α) Pd-RE ls equal to (ρ· α)Pd.The RE elements before Gd reduce the thermo-emf of Pd on Cu. other heavy RE enhance the thermo-emf.The experimental data of normalized Pd-0.1 at.-%RE alloys indicate that the effect of light RE additives on the specific resistivity of Pd is larger than that of heavy RE and Ce. Eu and Yb show anomalous strong effect. The valence and atomic size are main factors influencing the electrical properties.

Recent developments and applications on high-performance cast magnesium rare-earth alloys

During the past decades,with the increasing demands in lightweight structural materials,Mg alloys with low density and high performance have been extensively investigated and partly applied in some industries.Especially when rare earth(RE)elements are added as major alloying elements to Mg alloys,the alloy strength and creep resistance are greatly improved,which have promoted several series of Mg-RE alloys.This paper reviews the progress and developments of high-performance Mg-RE alloys in recent years with emphasis on cast alloys.The main contents include the alloy design,melt purification,grain refinement,castability,novel liquid casting and semisolid forming approaches,and the industrial applications or trials made of Mg-RE alloys.The review will provide insights for future developments of new alloys,techniques and applications of Mg alloys.

Corrosion rate determination of rare-earth Mg alloys in a Na_(2)SO_(4)solution by electrochemical measurements and inductive coupled plasma-optical emission spectroscopy

The corrosion resistance of three Mg alloys containing rare-earth elements(WE43,EV31 and ZE41)was studied and compared to that of two Mg-Al alloys(AZ31 and AZ91)and of pure Mg(99.95 wt.%).Current-voltage curves and electrochemical impedance measurements were performed with rotating disk electrodes in an aerated 0.1 M Na_(2)SO_(4)solution.For all the alloys,it was confirmed that the intermetallic particles acted as local cathodes and that more protective films were formed on the alloys surface by comparison with the pure Mg.Corrosion rates were determined from inductive coupled plasma-optical emission spectroscopy measurements and from the electrochemical measurements.Higher corrosion rates were observed for the rare-earth Mg alloys compared to the AZ series alloys.These data allowed the corrosion mechanisms to be discussed.

Research of Optical Performance On Rare-Earth Optical Fiber

The rare-earth optical fiber is made of organic material and inorganic rare earth material.It can be used to absorb and transfer solar energy.When sunlight irradiates, it may absorb and transfer solar energy automatically; while at night or without sunlight it may give out light and play role of decoration.By utilizing high transmissivity of organic material and heat-resisting performance of inorganic material, we know the reorganization of material performance under the melting condition, and make empty core bear the high temperature of 150 ~200 ℃.When the light spreads in light guide, some light energy travels along the direction of light guide, and is introduced in the room directly.Another part of light energy is absorbed and stored by light guide, and can release light again after 8 ~ 12 h.

Trace and rare earth element geochemistry of the black and grey shales of the Calabar Flank, Southeastern Nigeria: constraints on the depositional environment and the degree of metal enrichment

This study focuses on the trace and rare earth elements(REE)geochemistry of the Nkporo and Ekenkpon Shales of the Calabar Flank.The main aim is to infer their depositional environment and the degree of their metal enrichment.The shale samples were analyzed using inductively coupled plasma mass spectrometry.The results indicated that the mean concentrations of K,Na,and Fe in Nkporo and Ekenkpon Shales are 1.45,0.4,and 4.17 wt%,and 1.11,0.44,and 5.42 wt%;respectively.The Nkporo Shale is enriched with the following trace elements;P>Mn>Sr>Ba>Zn>Ce>Rb>Zr>V>Cr>Ni and depleted in the following trace elements;Ta>Ge>Sb>Bi>Cd>Ag>Te>In>Hg.While the Ekenkpon Shale is enriched with the following trace elements;P>Mn>Ba>Sr>V>Ce>Zr>Rb>Cr>Zn>Ni and depleted in;Sb>Ge>Bi>Ag>Ce>Te>In>Hg.The concentration of redox-sensitive elements such as V,Ni,Mo,U,Cu,Cr,Re,Cd,Sb,Ti,Mn,and their ratio V/Mo and U/Mo in the black and grey shale samples show different patterns.The REE obtained from the Nkporo and Ekenkpon Shales were PAAS normalized.The Nkporo Shale showed a slightly flat light rare-earth element(LREE),middle rare-earth element(MREE),and heavy rare earth element(HREE)pattern enrichment.Ce/Ce*ranges from 0.95 to 1.09 in Nkporo Shale and 0.67 to 1.40 in Ekenkpon Shale.The Ekenkpon Shale showed a slight LREE,MREE enrichment,and depleted HREE patterns.The Mn contents and U/Mo ratio in Nkporo and Ekenkpon Shales suggests a poor oxygen transitional environment.The V/Mo and V/(V+Ni)ratios indicated that the Nkporo shales were deposited in an anoxic to suboxic conditions and Ekenkpon shales were also deposited under an anoxic to suboxic conditions.The V/Ni ratio indicated that the organic matter in the Nkporo shale is terrigenous while that of the Ekenkpon shales are both terrigenous and marine in origin.

Applied Mineralogy Studies of Rare-Earth Ores

New attention has been given to the resources of rare earth minerals over the last years. The natural shortage of these elements in the Earth’s crust and trade restrictions recently imposed by China, motivated the Brazilian Government to encourage new projects by inserting the exploitation of rare earths in the National Mining Plan, which deals with industry strategic issues in the country, helping to reduce current importation. The incentives can be in the choice of future targets for mineral exploration and for the development of laboratory studies and pilot scale processing tests.

Mechanochemical-Assisted Leaching of Lamp Phosphors： A Green Engineering Approach for Rare-Earth Recovery

Rare-earth elements （REEs） are essential metals for the design and development of sustainable energy applications, Recycling these elements from waste streams enriched in them is crucial for securing an independent future supply for sustainable applications, This study compares the mechanisms of mechan- ical activation prior to a hydrometallurgical acid-leaching process and a solvometallurgical mechanochemical leaching process for the recovery of REEs from green lamp phosphor, LaPO4：Ce3＋, Th3＋, After 60 min of processing time, the REE leaching rates showed a significant enhancement of 60% after cycled mechanical activation, and 98% after the combined mechanochemical leaching process, High-resolution transmission electron microscopy （HR-TEM） imaging disclosed the cause for the improved REE leaching rates： The improved leaching and leaching patterns could he attributed to changes in the crystal morphology from monocrystalline to polycrystalline, Reduction of the crystallite size to the nanoscale in a polycrystalline material creates irregular packing of chemical units, resulting in an increase in defect-rich grain boundaries in the crystals, which enhances the leaching process, A solvometallurgical method was developed to combine the mechanical activation and leaching process into a single step, which is beneficial for operational cost, This results in an efficient and simple process that provides an alternative and greener recycling route for lamp phosphor waste,

Effect of Different N Sources on Contents of Rare Earth and Trace Elements in Sclerotia of Pleurotus Tuber Regium

Effect of different N resource on the contents of rare-earth elements, P, K and trace elements in the sclerotia of Pleurotus tuber regium was studied. The results show that the contents of rare-earth elements, P, K and trace elements in the sclerotia of Pleurotus tuber regium are different when treating with various N sources. Except Er and Tm, the contents of rare-earth elements of La, Ho, Dy, Tb and Yb are the highest by treating with ammonium sulfate. When concerning the contents of P, K and trace elements in the sclerotia in different N source treatments, the contents of Cu and Fe are the highest by using cow dung as N source, In and P are the highest by using ammonium sulfate, K, Cl and S are the highest when using urea as N source. The correlation analysis show that certain correlation exists among the contents of rare-earth elements, P, K and trace elements in the sclerotia of Pleurotus tuber regium. Furthermore, the correlation is different by using different N sources, among which the content of Dy is positively related with the contents of P and In, Yb is highly positively related with P content and La is negatively related with S content.

Study Segregation of Alloying Elements in Continuous Casting Slab with Valence Electron Structure

By calculating the electron structures of the phases that phosphor, sulfur and alloying elements dissolving inγ-Fe, the reason why alloying elements can bring centerline segregation in continuous casting slab (CCS) with nA, the number of electrons on the strongest covalent bonds, and the structure formation factor S were investigated, and an electron structural criterion to control and to eliminate the centerline segregation was advanced. Basing on this, the electron structures of a part of rare earth phosphides and sulfides are calculated, the physical mechanism that rare earth elements can control the segregation of phosphor and sulfur is analyzed, and the criterion is well verified.

稀土元素钬对蚕豆的细胞毒性和遗传毒性研究

运用氧化钬与稀硝酸反应制备结晶,以去离子水溶解并且稀释成梯度溶液,对蚕豆根尖染毒6h,分别修复培养22h和24h,观察根尖变化,统计微核率、染色体畸变率及有丝分裂指数。结果表明,4mg/L(以氧化钬质量体积浓度计)以下剂量对根尖生长具有促进作用;随着浓度的递增,微核率、染色体畸变率逐步上升,有丝分裂指数逐步下降,表现出明显的剂量 效应关系,说明稀土元素钬具有一定的细胞毒性和遗传毒性。同时,不同修复组在微核率、染色体畸变率及有丝分裂指数上也存在一定差异,表现为微核率22h修复组低于24h修复组,而染色体畸变率和分裂指数均高于24h修复组。微核检测应在染色体畸变检测之后进行。

稀土元素钬对小鼠3种抗氧化酶活力的影响

[目的]研究稀土元素钬对小鼠肝脏3种抗氧化酶活性的影响,找出剂量-效应关系.[方法]2次给小鼠腹腔注射氧化钬的盐酸溶液,相间24h,第2次注射24h后取肝脏检测超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)的活性,并进行统计分析,绘制出剂量-效应曲线.[结果]在10～40mg/kg体重剂量范围内3种酶的活性随剂量的增加而升高,40 mg/kg体重酶活性达峰值,与阴性对照比较,t检验显示差异极显著(P＜0.01);在40～160mg/kg体重剂量范围内3种酶的活性随剂量的增加而呈逐渐下降趋势.[结论]钬元素在低剂量下可能具有一定的抗氧化损伤作用,在高剂量时具有致抑制抗氧化酶活性的作用.

硝酸钬对小鼠骨髓细胞核异常和肝脏三种抗氧化酶活力的影响

两次给小鼠腹腔注射硝酸钬溶液,相间24h,第二次注射24h后取股骨骨髓涂片,同时取肝脏检测超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)活力。结果发现,在(10～40)mg/kg·bw剂量范围内,微核率和三种酶的活力随剂量的增加而升高;当剂量升至80mg/kg·bw时,三种酶活力趋于下降,但仍高于阴性对照组,而微核率增加到最大值;当剂量升至160mg/kg·bw时,微核率和酶活力均低于阴性对照组。低剂量(<40mg/kg·bw)硝酸钬溶液可促进骨髓细胞增殖,高浓度则表现出抑制作用。实验中还观察到核异常程度随剂量的增加而上升。推测低剂量钬离子通过诱导小鼠机体三种抗氧化酶活力的升高,清除部分自由基,一定程度上减轻了染色体损伤,高剂量则抑制了细胞分裂指数,又降低小鼠体内抗氧化酶活力,从而促进核异常。

稀土元素原子发射光谱及其谱线干扰的高分辨率ICP-AES研究——Ⅵ.镧、铽、钬、铒基体对其他稀土元素的光谱干扰

利用光栅刻线为 3 6 0 0条 /mm的高分辨率时序扫描式ICP AES光谱仪研究镧 (La)、铽 (Tb)、钬(Ho)、铒 (Er)基体分别对其他 14个稀土元素共 6 5条“首选分析线”的光谱干扰情况。获得了相应的光谱干扰轮廓和稀土光谱干扰信息 ,为选择在该 4种稀土基体中的其他稀土元素ICP AES最佳分析线提供了参考。

火花源质谱法定量分析高纯氧化钬和氧化镥中痕量元素

本文采用相对灵敏度因子，研究了９９．９９９％－９９．９９９９％的Ｈｏ２Ｏ３和Ｌｕ２Ｏ３中４０余种杂质元素的火花源定量分析方法，讨论了谱线干扰。做了加入回收及生理性实验，大多数元素的相对标准偏差在３０％以内，检测下限为０．００ｘμｇ／ｇ。