Rare earth separations by selective borate crystallization

نویسندگان

  • Xuemiao Yin
  • Yaxing Wang
  • Xiaojing Bai
  • Yumin Wang
  • Lanhua Chen
  • Chengliang Xiao
  • Juan Diwu
  • Shiyu Du
  • Zhifang Chai
  • Thomas E. Albrecht-Schmitt
  • Shuao Wang
چکیده

Lanthanides possess similar chemical properties rendering their separation from one another a challenge of fundamental chemical and global importance given their incorporation into many advanced technologies. New separation strategies combining green chemistry with low cost and high efficiency remain highly desirable. We demonstrate that the subtle bonding differences among trivalent lanthanides can be amplified during the crystallization of borates, providing chemical recognition of specific lanthanides that originates from Ln3+ coordination alterations, borate polymerization diversity and soft ligand coordination selectivity. Six distinct phases are obtained under identical reaction conditions across lanthanide series, further leading to an efficient and cost-effective separation strategy via selective crystallization. As proof of concept, Nd/Sm and Nd/Dy are used as binary models to demonstrate solid/aqueous and solid/solid separation processes. Controlling the reaction kinetics gives rise to enhanced separation efficiency of Nd/Sm system and a one-step quantitative separation of Nd/Dy with the aid of selective density-based flotation.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Molecular Recognition Technology: a Green Chemistry Process for Separation of Individual Rare Earth Metals

Separation methods for rare earth elements (REE) are predominantly based on solvent extraction procedures. These methods are low in metal selectivity and generate large amounts of waste resulting in high capex and opex costs. Molecular Recognition Technology (MRT) is a much simpler green chemistry process that uses no organic solvents and carries out separations with highly metal-selective Supe...

متن کامل

Ca3Be6B5O16F: the first alkaline-earth beryllium borate with fluorine anions.

The first all-alkaline-earth beryllium borate with fluorine anions, Ca3Be6B5O16F, was synthesized by a spontaneous crystallization flux method using LiF-B2O3 as the flux. The structural framework of Ca3Be6B5O16F is composed of the inter-connected [Be6B3O16] and [BO3] fundamental building blocks, with [CaO7F] distorted polyhedra located in the interstitial sites. The [Be6B3O16] group is discover...

متن کامل

Growth and properties of rare-earth arsenide InGaAs nanocomposites for terahertz generation

Articles you may be interested in Lattice distortion in single crystal rare-earth arsenide/GaAs nanocomposites Appl. Dielectric and optical properties of epitaxial rare-earth scandate films and their crystallization behavior Appl.

متن کامل

PREBIOTIC CHEMISTRY Borate Minerals and Origin of the RNAWorld

The RNA World is generally thought to have been an important link between purely prebiotic (>3.7 Ga) chemistry and modern DNA/protein biochemistry. One concern about the RNAWorld hypothesis is the geochemical stability of ribose, the sugar moiety of RNA. Prebiotic stabilization of ribose by solutions associated with borate minerals, notably colemanite, ulexite, and kernite, has been proposed as...

متن کامل

Ln(III) methyl and methylidene complexes stabilized by a bulky hydrotris(pyrazolyl)borate ligand.

The reaction of Ln(AlMe(4))(3) with bulky hydrotris(pyrazolyl)borate (Tp(t)(Bu,Me))H proceeds via a sequence of methane elimination and C-H bond activation, affording unprecedented rare-earth metal ligand moieties including Ln(Me)[(micro-Me)AlMe(3)] and X-ray structurally characterized "Tebbe-like" Ln[(micro-CH(2))(2)AlMe(2)].

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2017