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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2019 · IF 3.375

Extraction of Rb(I) Ions from Aqueous Solution Using Novel Imprinting Materials

Xingwen Liu,Qi Wang,Zhuo Wang,Xueting Liu,Minghui Zhang,Jiahui Fan,Zhiyong Zhou,Zhongqi Ren

A new type of Rb(I) ion imprinting material was prepared with methacrylic acid as functional monomer, Rb(I) ion as template, and methanol/acetonitrile as solvent. The polymerization reaction was initiated by N,N-azobis(isobutyronitrile) (AIBN) with the cross-linking by ethylene glycol dimethacrylate (EGDMA). In addition, benzo-12-crown-4-ether (B12C4) was introduced as a ligand to fix the template ions better. Scanning electron microscope, Zeta potential analysis, Fourier transform infrared spectrum, thermogravimetric analysis, and energy dispersive spectra were used for characterization of the imprinted polymer. Effects of preparation and adsorption conditions on adsorption performances of Rb(I) ion-imprinted polymers (IIPs) were investigated. The imprinted polymer had fast adsorption kinetics (reaching equilibrium within 15 min) and high maximum adsorption capacity (129.9 mg·g–1) at pH 9.5. Besides, the adsorption process conformed to pseudo-second-order kinetic and Freundlich isotherm models. Moreover, the prepared Rb(I)-IIPs showed high selectivity for Rb(I) ions. The results of eight repeated cycles of adsorption–desorption demonstrated that the prepared Rb(I)-IIPs had good stability and reusability.

研究领域: 化学 · 环境科学
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POLYHEDRON · 2019 · IF 2.284

Highly efficient capture of rubidium ion by a novel HS-Fe3O4@MIL-53(Al) composite material

Ning Tian,Yifang Dai,Qing Liu,Wei Dai

A general synthetic strategy for HS-Fe 3 O 4 @MIL-53(Al) adsorbent has been developed in this work. The composite material exhibits an efficient capture performance for rubidium ion due to sulfhydryl group and magnetic Fe 3 O 4 doped in its porous cavity. The results of X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and N 2 adsorption–desorption proved that the HS-Fe 3 O 4 was immobilized in the composite material. High Rb + uptake capacity over the HS-Fe 3 O 4 @MIL-53(Al) is attributed to the exchange of acidic protons between the sulfhydryl group and the Rb + . The pseudo-second-order and Freundlich model could make a good description of the adsorption process. The Rb + sorption selectivity was moderately influenced by any co-ions effect (K + , Na + and Cs + ) due to HS-Fe 3 O 4 doped. These results reveal that our novel composite material might be a promising industrial adsorbent for Rb + capture.

研究领域: 材料科学 · 环境科学
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ACS Applied Nano Materials · 2025 · IF 5.5

Enhanced Luminescence of CsPbBr3 Quantum Dot Glass through Eu3+–Rb+ Codoping

Jingyi He,Shimin Liu,Jianmin Gu,Shiqing Xu

All-inorganic lead halide perovskite quantum dots (CsPbX3 QDs, X = Cl, Br, I) glass has elicited extensive attention due to its excellent stability. However, the realization of CsPbX3 QDs glasses with a high photoluminescence quantum yield (PLQY) remains a challenging task. In this study, Eu3+ ions act as nucleating agents to promote the formation and crystallization of CsPbBr3 QDs. Rb+ ions further improve the crystallization quality and reduce the defects between CsPbBr3 QDs and the glass interface. The codoping of Eu3+ and Rb+ ions greatly improved the PLQY of CsPbBr3 QDs. The highest PLQY is achieved in the 0.33Rb-2Eu heat-treated at 500 °C–6 h, reaching 54%. Furthermore, among the light-emitting diodes (LEDs) prepared with 1Cs-0Eu, 1Cs-2Eu, or 0.33Rb-2Eu, 0.33Rb-2Eu has the highest color gamut coverage (108.9% of the National Television Standards Committee color gamut and 92.7% of Rec. 2020 color gamut at 20 mA) and the strongest durable high-power driving capability, making it an ideal material for green LEDs.

研究领域: 材料科学 · 光学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2020 · IF 5.774

Mixed matrix membranes for rubidium-dependent recognition and separation: A synergistic recombination design based on electrostatic interactions

Chao Yu,Jian Lu,Zhiqiang Hou,Zhongfei Ma,Xinyu Lin,Zeqing Dong,Wendong Xing,Yongsheng Yan,Yilin Wu

Exposure and distribution of recognition sites are critical for membrane separation materials to enhance adsorption and separation efficiency toward rubidium ion. Herein, we prepared the rubidium (Rb) ion separation membranes (Rb-ISMs) through a delayed phase inversion method taking advantage of the different polarities between ethanol and water. Fabrication process was conducted through immersion of a poly (vinylidene fluoride)/graphene oxide (PVDF/GO) casting solution into coagulating bath containing 18-crown-6 (18C6) grafted mesoporous silica, ethanol and water. After phase inversion process, the as-prepared adsorbent materials were immobilized on membrane surface by strong electrostatic interaction force. The method could effectively avoid the embedding and aggregation recognition sites, and the coagulating bath only required the ethanol and water that was relatively healthy and environmental. The Rb-ISMs prepared at optimal conditions showed enhanced rebinding capacity (49.344 mg g −1 ) towards Rb ± , with a superior rebinding selectivity (11.8, 6.82, 9.08 for Rb ± /Ca 2+ , Rb ± /Cs ± , Rb ± /Mg 2+ , respectively). Importantly, Rb-ISMs showed remarkable perm-selectivity and regeneration performance, which further demonstrated its potentials in the rapid and effective separation field of Rb ions.

研究领域: 材料科学 · 环境科学
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APPLIED ORGANOMETALLIC CHEMISTRY · 2019 ·Vol. 33 ·期 3 ·e4778 · IF 3.259

Simultaneous adsorption of Li(I) and Rb(I) by dual crown ethers modified magnetic ion imprinting polymers

Jicheng Xu,Zhilong Pu,Xuechao Xu,Yuanyuan Wang,Dongya Yang,Tao Zhang,Fengxian Qiu

With the gradual exhaustion of land mineral resources, oceans and lakes have attracted world attention because they are abundant in inorganic mineral resources including lithium, potassium, rubidium and cesium. Lithium is becoming the key material in manufacturing of primary and secondary batteries used in various portable devices and hybrid/electric vehicles. Rubidium has been widely applied inglobal positioning satellites, magneto-optic modulators, solid-state lasers, phosphors, and glass manufacturing. In this work, a novel dual-functional magnetic ion imprinting polymer (Fe 3 O 4 @SiO 2 @IIPs) powder was prepared using 12-crown-4 (12C4) and 18-crown-6 (18C6) as functional monomer, and characterized by FT-IR, elemental analysis, XRD, TGA, SEM and TEM. The adsorption performance of Fe 3 O 4 @SiO 2 @IIPs for simultaneous adsorption of lithium and rubidium from simulative salt lakes was evaluated by batches of experiments at various pH values, contact time, and initial concentrations. Kinetic experiments show that the adsorption process followed the pseudo second order kinetic model. Langmuir adsorption isotherm model and Freundlich adsorption equilibrium data were fitted; the results show that Langmuir isotherm model is more suitable for the adsorption process. Additionally, Fe 3 O 4 @SiO 2 @IIPs exhibit specificity towards Li(I) and Rb(I) and low competitive behavior with Na(I), K(I) and Mg (II). Additionally, the selectivity properties, reusability and adsorption thermodynamic were also investigated. The obtained results show that the prepared Fe 3 O 4 @SiO 2 @IIPs material remains high adsorption capacities after five cycles, exhibits excellent abilities to simultaneously and selectively recover Li + and Rb + and have a promising application in the simultaneous adsorption of lithium and rubidium ions.

研究领域: 材料科学 · 环境科学
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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

Tunable superporous magnetic adsorbent prepared via eco-friendly Pickering MIPEs for high-efficiency adsorption of Rb+ and Sr2+

Taotao Lu,Yongfeng Zhu,Yanxing Qi,Yuru Kang,Aiqin Wang

Until recently, high organic phase volume and the addition of a large amount of surfactants have been two major disadvantages of conventional high internal phase emulsions (HIPEs) templates in the construction of porous adsorbents. Herein, a facile and novel tunable superporous magnetic adsorbent (MSPA) was synthesized by the polymerization of the green surfactant-free (soybean oil)-in-water Pickering medium internal phase emulsion (O/W Pickering MIPEs), which was stabilized synergically by the magnetic yeast (MY) and chitosan (CTS). It is interesting that the extremely stable surfactant-free Pickering-MIPEs can be obtained through the fine synergistic effect between MY and CTS at the oil-water interface, and the pore structure of the magnetic adsorbent can be easily adjusted by changing the ratio of MY to CTS, as well as the external pH. The obtained MSPA with abundant COO − and NH 2 functional groups had a fast capture rate and high adsorption capacities for radioactive Rb + and Sr 2+ ions, respectively. The saturation adsorption capacities of 168.98 and 151.91 mg/g for Rb + and Sr 2+ can be achieved within 25 or 10 min, respectively. Moreover, the MSPA had excellent regeneration ability and reusability. This work provided a feasible and environmentally friendly pathway for preparation of the superporous magnetic adsorbent with tunable porous structure for adsorption and separation application.

CAS / MDL: 3326-32-7 3625-57-8
研究领域: 环境科学 · 材料科学
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Journal of Physical Chemistry C · 2022 · IF 4.177

In Situ Synthesis of UltraStable TiO2 Coating Rb+-Doped Red Emitting CsPbBrI2 Perovskite Quantum Dots

Yongqiang Ji,Minqiang Wang,Zhi Yang,Hao Wang,Muhammad Amin Padhiar,Jindou Shi,Hengwei Qiu,Arshad Saleem Bhatti

Among the lead halide perovskites, the stability of red-emitting CsPbBrI2 perovskite quantum dots (PQDs) is very poor. This is an impediment to the development of high purity white emitting diodes (WLEDs) based on PQDs. Herein, we surprisingly find that luminescent properties of CsPbBrI2 PQDs can be significantly improved through doping of univalent Rb+ ions, especially when molar ratio of Rb+/Cs+ = 0.1/0.9. Subsequently, these red emitting Rb0.1Cs0.9PbBrI2 PQDs are successfully coated with TiO2 through an easy in situ strategy of adding titanium(IV) butoxide (TBO) to the precursor. Benefiting from the efficient protection of TiO2 nanoshell, these highly fluorescent Rb0.1Cs0.9PbBrI2/TiO2 nanocomposites can preserve their excellent red emitting characteristics even when directly immersed in water or exposed to illumination, enabling us to build highly stable WLEDs with color coordinates at (0.342, 0.325).

研究领域: 材料科学 · 光学工程
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ACS Nano · 2024 · IF 15.8

Trifunctional Rb+-Intercalation Enhancing the Electrochemical Cyclability of Ammonium Vanadate Cathode for Aqueous Zinc Ion Batteries

Kai Wang,Shijia Li,Xue Chen,Jiasen Shen,Huiling Zhao,Ying Bai

Rechargeable aqueous zinc-ion batteries (AZIBs) have been highly desired due to their low cost, intrinsic safety, environmental friendliness, and great potential in large-scale power storage systems. However, their practical applications are impeded by unstable long-term electrochemical performances induced by microstructure degradation of the cathode material, hydrogen evolution reaction in the electrolyte, and dendritic growth on the zinc anode upon cycling. In this work, rubidium cations (Rb+) are introduced to synthesize an Rb+-preintercalated NH4V4O10 (NVO-Rb) composite. The contribution of Rb+ ions as pillars in V–O interlayers to facilitating Zn2+ storage is investigated first, and then the influences of partial Rb+ ions from the NVO-Rb cathode on the aqueous electrolyte and zinc anode are specially inspected from different viewpoints. Based on a series of characterization results, it is comprehensively elucidated that the partial Rb+ ions into the electrolyte suppress the generation of byproducts on the cathode and regulate the dendrite growth on the zinc anode, thus effectively promoting the long-term electrochemical performances of NVO-based AZIBs. The assembled Zn∥Zn(CF3SO3)2∥NVO-Rb cell can exhibit a high specific capacity and optimized Zn2+ diffusion kinetics, especially an improved electrochemical cyclability with a capacity retention of 87.6% at 5 A g–1 over 10000 cycles. This study enlightens the multiple roles of cation-preintercalation in the layered structure material and provides a feasible strategy for the development of high-performance aqueous batteries.

研究领域: 材料科学 · 电化学
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JOURNAL OF SOLID STATE CHEMISTRY · 2021 · IF 3.498

Ammonium molybdophosphate/metal-organic framework composite as an effective adsorbent for capture of Rb+ and Cs+ from aqueous solution

Yanping Wang,Kexin Li,Dezhen Fang,Xiushen Ye,Haining Liu,Xiaoli Tan,Quan Li,Jun Li,Zhijian Wu

A new composite adsorbent (AMP@MOF-76(Sm)) grafted ammonium molybdophosphate onto MOF-76(Sm) was synthesized via a solvothermal method and well-characterized by SEM-EDS, particle size analysis , N 2 adsorption-desorption isotherms, TG, FT-IR, XRD and XPS analysis . The adsorption behaviors of Rb + and Cs + on synthesized AMP@MOF-76(Sm) were investigated depending on the parameters of solution pH, ionic strength, contact time, ion concentration and temperature. The adsorbent can adsorb Rb + and Cs + from the solution when the solution pH ranged from 4.0 to 10.0 and the coexisted ion (Na + ) has little effect on the adsorption amounts of both Rb + and Cs + . The adsorption kinetic data fitted well with pseudo-second order kinetic models . The adsorption equilibrium of Rb + and Cs + on AMP@MOF-76(Sm) is better explained by the Langmuir isotherm model and the maximum adsorption amounts for Rb + and Cs + are 0.490 ​mmol ​g −1 and 0.434 ​mmol ​g −1 , respectively. Furthermore, the AMP@MOF-76(Sm) could be easily reused at least four times using 3.0 ​mmol ​L −1 ammonia nitrate as the eluent . The mechanism of the adsorption of Rb + and Cs + is proposed to be a combination of electrostatic attraction and ion exchange mechanism.

研究领域: 环境科学 · 材料科学
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INORGANIC CHEMISTRY · 2021 · IF 5.165

Two Lead Halides with Strong SHG Response Obtained by the Isovalent Substitutions of Alkali Metal Cation and Halogen Anion

Qirui Shui,Ruibiao Fu,Hongxin Tang,Yuanbin Fang,Zuju Ma,Xintao Wu

The substitution of alkali metal cation or halogen anion based on nonlinear crystals is an effective strategy to exploit new optical materials. The strategy has been successfully expanded to discover two new lead halides, Rb3Pb2(CH3COO)2X5 (X = Br, Cl). The substitution of the Cs+ cation with a Rb+ cation can not only increase the local dipole moment of the distorted [PbBr4O2] polyhedron but also reduce the cell unit, resulting in a large net macroscopic polarization. Therefore, Rb3Pb2(CH3COO)2Br5 possesses a strong second-harmonic generation (SHG) response (6 × KDP) and a large birefringence (0.18@1064 nm). Furthermore, by the substitution of the Br– anion with a Cl– anion, Rb3Pb2(CH3COO)2Cl5 exhibits a high laser damage threshold (LDT, 84 × AgGaS2) and a short UV cutoff edge of 287 nm, as well as moderate SHG response (3 × KDP) and birefringence (0.11@1064 nm). Detailed theory calculations elucidate the origin of the linear and nonlinear optical properties of these compounds.

研究领域: 材料科学 · 光学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

The protonated 2 × 4 tunnel manganese oxide nanobelts for high-efficient electrochemical rubidium enrichment

Xiaohui Wang,Xue Wang,Yali Wang,Quanguo Zhai,Yucheng Jiang,Shuni Li

Octahedral molecular sieve – 5 (OMS-5), a typical 2 × 4 tunnel manganese oxide, is considered as an adsorbent for rubidium ion (Rb + ) because of its specific tunnel structure. Also, manganese oxide-based nanomaterials are also widely used in supercapacitor energy storage and capacitor deionization electrodes due to their high specific capacitance. In this work, a series of protonated OMS-5 (H-OMS-5, H-Co-OMS-5, and H-Ni-OMS-5) nanobelts are synthesized and used as electrode materials for electrochemical enrichment of Rb + in aqueous solution. The specific capacity values for H-OMS-5, H-Co-OMS-5, and H-Ni-OMS-5 at 1 A·g −1 are of 159, 168, and 215 F·g −1 , respectively. Thanks to the unique protonated 2 × 4 tunnel structure, well regulating surface area, and excellent specific capacitance, the maximum Rb + adsorption capacities of H-OMS-5, H-Co-OMS-5, and H-Ni-OMS-5 can reach to 390.3, 405.7, and 481.7 mg·g −1 , respectively. These results indicate that the protonated 2 × 4 tunnel manganese dioxide nanobelts are of great potentials as faradaic electrode materials for selective rubidium ion enrichment applications.

研究领域: 材料科学 · 环境科学 · 电化学
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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2024 · IF 3.7

Removal of rubidium from brine by an integrated film of sulfonated polysulfone/graphene/potassium copper ferricyanide

Huanxi Xu,Peihua Lin,Pei-Jun Liu,Hai-Gang Liu,Hui-Bin Guo,Chao-Xiang Wu,Ming Fang,Xu Zhang,Guan-Ping Jin

A novel integrated film of sulfonated polysulfone/graphene/potassium copper ferricyanide (KCuFC/SPSG) was used for selectively extracting rubidium ion (Rb + ) from brine. To form KCuFC/SPSG, the precursor film of sulfonated polysulfone/graphene (SPSG) was synthesized by phase conversion process, which was alternately immersed in 0.1 mol·L –1 CuSO 4 /K 4 [Fe(CN) 6 ] by in-situ adsorption coupled co-precipitation method. Various data such as nuclear magnetic resonance spectrometer, Fourier transform infrared spectroscope, X-ray photoelectron spectroscope, X-ray diffraction, scanning electron microscope and energy dispersive spectroscopy all verified that abundant KCuFC were uniformly located on the film. The resulting KCuFC/SPSG was used in film separation system. As the solution was fed into the system, the Rb + could be selectively adsorption by KCuFC/SPSG. After the saturation adsorption, 0.5 mol·L –1 NH 4 Cl/HCl was fed into the film cell, Rb + could be quickly desorbed by ion-exchange between Rb + and NH 4 + in the lattice of KCuFC. The purpose of separating and recovering Rb + from the brine can be achieved after the repeated operation. The effects of pH, adsorption time and interferential ions on the adsorption capacity of Rb + were investigated by batch experiments. The adsorption behavior fits the pseudo-second order kinetic process, while KCuFC has a higher adsorption capacity (Langmuir maximum sorption 165.4 mg∙g –1 ). In addition, KCuFC/SPSG shows excellent selectivity for Rb + even in complex brine systems. KCuFC/SPSG could maintain 93.5% extraction efficiency after five adsorption/desorption cycles.

研究领域: 材料科学 · 环境科学
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