Transformation of Coal Gangue to Sodalite and Faujasite Using Alkali-hydrothermal Method

The coal gangue as the only source of silicon and aluminum was employed to synthesize sodalite and faujasite using hydrothermal method,which directly treated the mixture of pre-treated coal gangue and NaOH solution under hydrothermal environment.X-ray powder diffraction analysis(XRD),thermogravimetry analysis(TG)and differential thermogravimetry analysis(DTG),scanning electron microscopy(SEM),high resolution transmission electron microscopy(HRTEM),N_(2)adsorption-desorption technique,X-ray photoelectron spectroscopy(XPS),etc.were used to characterize the samples.Cd^(2+) ion was used to evaluate the heavy metal ions removal performance of the samples.The experimental results show that the coal gangue,which consists of quartz,calcium feldspar,potassium feldspar and kaolinite,can transform to sodalite and faujasite under alkali-hydrothermal condition at 150 and 180℃,respectively.The as-prepared sodalite and faujasite can effectively remove the simulated Cd2+ion wastewater and actual industrial wastewater containing As^(3+),Cd^(2+),and Cr^(3+)ions,and the good heavy metal ion removal performance of the zeolites is mainly attributed to their low Si/Al ratio and high Na+content.This alkali-hydrothermal method appears to be a simple and efficient method for transformation of coal gangue to high purity zeolites.

Faujasite沸石纳米棒的合成及其对重金属的吸附

通过优化水热合成条件成功合成出具有八面纳米棒形貌的Faujasite沸石材料(长度300~900 nm,截面宽度20~50 nm),该材料的理论分子式为Na_(14)Al_(12)Si_(13)O_(51)·6H_(2)O。将此沸石材料用于溶液中重金属离子的吸附研究,结果表明:该沸石材料对Cu^(2+)、Cd^(2+)、Pb^(2+)和Ni^(2+)的极限吸附量分别为250、323、1 075和256 mg/g。吸附过程在开始后的100分钟内达到吸附平衡,溶液pH的提高可以促进表观吸附。准二级动力学方程和Langmuir吸附等温线能够良好地拟合沸石材料对四种重金属离子的吸附过程。DFT模型计算结果显示,各重金属吸附构型的稳定性和吸附过程发生的趋势顺序均为Pb>Cd>Ni>Cu。

Faujasite zeolite decorated with cobalt ferrite nanoparticles for improving removal and reuse in Pb^2+ions adsorption

Water pollution caused by heavy metals ions has been gaining attention in recent years,increasing the interest in the development of methodologies for their efficient removal focusing on the adsorption process for these purposes.The current challenge faced by adsorption processes is the adequate adsorbent immobilization for removal and reuse.Thus,the present work aimed at producing a faujasite zeolite nanocomposite decorated with cobalt ferrite nanoparticles for Pb^2+ions adsorption in an aqueous medium improving magnetic removal and reuse.As a result,a high surface area(434.4 m^2·g^-1)for the nanocomposite and an 18.93 emu·g^-1 saturation magnetization value were obtained,indicating magnetic removal in a promising material for adsorption process.The nanocomposite regeneration capacity evaluated by magnetic recovery after 24 h suspension presented a high Pb^2+ion adsorptive capacity(98.4%)in the first cycle.Around 98%of the Pb^2+ions were adsorbed in the second cycle.In this way,the synthesized faujasite:cobalt ferrite nanocomposite reveals itself as a promising alternative in adsorption processes,aiming at a synergic effect of FAU zeolite high adsorptive activity and the cobalt ferrite nanoparticles magnetic activity,allowing for adsorbent recovery from the aqueous medium via magnetic force and successive adsorptive cycles.

Mesoporous activated carbon-zeolite composite prepared from waste macadamia nut shell and synthetic faujasite

Novel activated carbon-zeolite composite adsorbent was prepared from macadamia shell bio-waste and synthetic zeolite X using hydrothermal treatment.Characterisation studies revealed mainly mesoporous structure with 418 m^2·g^(-1) BET surface area with faujasite clusters on the carbon carrier.Sorption capacity for methylene blue model pollutant increased from 85 to 97 mg·g^(-1) with the temperature increase from 25 to 45 ℃, and improved with increasing pH.Nonlinear regression analyses found accurate fit to the pseudo-first-order kinetics model and intra-particle diffusion rate controlling mechanism.Excellent fits to the Jovanovic isotherm model indicated monolayer coverage on chiefly homotattic surfaces with variable potential.The thermodynamic analysis confirmed spontaneous and endothermic physisorption process.The spent adsorbent was regenerated with 20% capacity loss over five reuse cycles.Although the adsorbent was developed for ammonia, heavy metal and organic matter removal from water sources, the results also indicate good performance in cationic dye removal from wastewaters.

Synthesis of Faujasite from Egyptian Clays: Characterizations and Removal of Heavy Metals

Three clay samples with different mineral compositions (kaolinite, smectite-kaoline, and smectite-rich) were used for zeolite synthesis using the method of hydrothermal reactions after fusion with NaOH. The conditions of hydrothermal crystallization (zeolitization) were found to be at temperature of 100°C, and time span between 72 h and 96 h for kaoline and smectite-rich samples, while 48 h for the smectite-kaolinite sample. The results indicate that zeolites began to crystallize from clay samples after 48 h, and crystallization increased with increasing time. The synthetic materials have been characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), fourier transform infrared spectroscopy (FT-IR) and thermogravimetric (DTA/TGA) analysis. The results indicate that low silica NaX-faujasite type with well-developed octahedral and cubic crystals was synthesized from the three samples. No big difference in the characterization between the three synthetic materials was detected, but smectite-kaolinite sample as raw material was relatively better in crystallization of synthetic zeolite. Applications of the synthetic materials in the removal of heavy metals proved that the synthetic faujasite has strong effect for removing of Cr3+, Co2+, Ni2+ and Mn2+ from aqueous solution.

Study of the Temperature-Programmed Desorption of Carbon Dioxide (CO2) on Zeolites X Modified with Bivalent Cations

Study of physisorbed and chemisorbed carbon dioxide (CO2) species was carried out on the NaX zeolite modified by cationic exchanges with bivalent cations (Ca2+ and Ba2+) by temperature-programmed desorption of CO2 (CO2-TPD). Others results were obtained by infrared to complete the study. The results of this research showed, in the physisorption region (213 - 473 K), that the cationic exchanges on NaX zeolite with bivalent cations increase slightly the interactions of CO2 molecule with adsorbents and/or cationic site. Indeed, the desorption energies of physisorbed CO2 obtained on the reference zeolite NaX (13.5 kJ·mol-1) are lower than that of exchanged zeolites E-CaX and E-BaX (15.77 and 15.17 kJ·mol-1 respectively). In the chemisorbed CO2 region (573 - 873 K), the desorption energies related to desorbed species (bidentate carbonates: CO32-) on the exchanged zeolites E-CaX and E-BaX are about 81 kJ·mol-1, higher than the desorbed species (bicarbonates: HCO32-) on the reference R-NaX (62 kJ·mol-1). In addition, the exchanged E-BaX zeolite develops the secondary adsorption sites corresponding to bicarbonates species with desorption energies of 35 kJ·mol-1 lower to desorption energies of bicarbonates noted on the reference zeolite NaX.

原位晶化法制备整体式FAU分子筛

采用原位晶化法制备了整体式FAU分子筛,系统考察了合成体系的n（SiO2）/n（Al2O3）、n（Na2O）/n（SiO2）、n（H2O）/n（Na2O）、晶化温度和时间对整体式FAU分子筛结晶度的影响规律。结果表明,在所考察的范围内,随着合成体系的n（SiO2）/n（Al2O3）增加和n（Na2O）/n（SiO2）的减小,整体式FAU分子筛结晶度逐渐升高;随着n（H2O）/n（Na2O）的增大,整体式FAU分子筛结晶度呈现先升高后降低趋势。晶化温度从80℃逐渐增加至100℃时,整体式FAU分子筛结晶度也随之升高;初始产物结晶度较低（02h）,然后随着晶化时间的延长急剧升高（27h）,最后基本保持不变（】7h）。按照较优的合成体系配比和晶化条件合成出了高纯度、高结晶度的整体式FAU分子筛。

Hydrothermal Synthesis and Properties of Y-zeolite-containing Composite Material with Micro/mesoporous Structure

A Y-zeolite-containing composite material with micro/mesoporous structure had been synthesized from kaolin by means of the in-situ crystallization method. The obtained samples were investigated by XRD and BET methods. Evaluation of catalytic activity of both the commercial Y-zeolite and the novel Y-zeolite-containing composite material was carried out in the pulse micro-chromatography platform with two probe molecules of different molecular sizes： VGO feedstock and 1,3,5 tri-isopropyl benzene. It was found that the Y-zeolite-containing composite material was richer in external surface and meso-/macro-pores; the Y-zeolite-containing composite material demonstrated a smaller rate of deactivation compared to the commercial Y-zeolite.

Super-Hydrides of Lanthanum and Yttrium: On Optimal Conditions for Achieving near Room Temperature Superconductivity

Recently, many seminal papers deal with the syntheses, stability and superconducting properties of super-hydrides like LaH10 or YH10 under high pressure, reporting critical temperatures near room temperature. In the first run one will assume that the involved metal atoms contribute a number of 3 electrons to the pairing pool corresponding to their valence. However, another possibility may be that the cationic valence is somewhat smaller, for instance only 2.29, resulting in a nominal electron number per cation of σ0 = 0.229 ≈ 3/13 instead of 0.3. Then, we will have a numerical equality to the optimum hole number in the cuprate high-Tc superconductors, a number that reflects the fractal nature of electronic response in superconductors. However, if one still keeps up the oxidation state of +3 of lanthanum, one will need 13 hydrogen atoms to match the optimum σ0. Such composition may be found at the phase boundary between the observed LaH10 and LaH16 phases. Partial ionic replacement is suggested to shift the super-hydride composition into the σ0 optimum. Micro-structural phenomena such as multiple twinning and ferroelastic behavior as observed with cuprates may also influence the superconductivity of super-hydrides. Finally, epitaxial growth of super-hydrides onto a specially cut diamond substrate is proposed.