Fabrication of pollution-free coal gangue-based catalytic material utilizing ferrous chloride as activator for efficient peroxymonosulfate activation

Novel coal gangue-based persulfate catalyst(CG-FeCl_(2))was successfully synthesized by the means of calcinating under nitrogen atmosphere with the addition of ferrous chloride tetrahydrate(FeCl_(2)·_(4)H_(2)O).The phase transformation of the prepared materials and gas products during the heating process are thoroughly investigated.It is suggested that ferrous chloride participated in the phase transformation and formed Si-O-Fe bonds.And the main gaseous products are H_(2)O,H_(2),and HCl during the heating process.Besides,the ability of CG-FeCl_(2) to activate peroxymonosulfate(PMS)for catalytic degradation of polycyclic aromatic hydrocarbons(PAHs)and phenol was deeply studied.More than 95%of naphthyl,phenanthrene and phenol were removed under optimizied conditions.In addition,1O_(2),·OH,and SO_(4)·−were involved in the CG-FeCl_(2)/PMS system from the free radical scavenging experiment,where 1O_(2) played a major role during the oxidation process.Furthermore,CG-FeCl_(2)/PMS system exhibited superior stability in a relatively wide pH range and the presence of common anion from related degradation experiments.Overall,the novel CG-FeCl_(2) is an efficient and environmentally friendly catalyst,displaying potential application prospect in the field of PAHs and phenol-contaminated wastewater treatment.

Research progress of CO_(2) capture and mineralization based on natural minerals

Natural minerals,such as kaolinite,halloysite,montmorillonite,attapulgite,bentonite,sepiolite,forsterite,and wollastonite,have considerable potential for use in CO_(2) capture and mineralization due to their abundant reserves,low cost,excellent mechanical prop-erties,and chemical stability.Over the past decades,various methods,such as those involving heat,acid,alkali,organic amine,amino sil-ane,and ionic liquid,have been employed to enhance the CO_(2) capture performance of natural minerals to attain high specific surface area,a large number of pore structures,and rich active sites.Future research on CO_(2) capture by natural minerals will focus on the full utiliza-tion of the properties of natural minerals,adoption of suitable modification methods,and preparation of composite materials with high specific surface area and rich active sites.In addition,we provide a summary of the principle and technical route of direct and indirect mineralization of CO_(2) by natural minerals.This process uses minerals with high calcium and magnesium contents,such as forsterite(Mg_(2)SiO_(4)),serpentine[Mg_(3)Si_(2)O(OH)_(4)],and wollastonite(CaSiO_(3)).The research status of indirect mineralization of CO_(2) using hydro-chloric acid,acetic acid,molten salt,and ammonium salt as media is also introduced in detail.The recovery of additives and high-value-added products during the mineralization process to increase economic benefits is another focus of future research on CO_(2) mineralization by natural minerals.

上扬子北缘川北地区结晶基底晶质石墨矿数据集

上扬子北缘川北地区出露的基底地层发育双层结构,其中上层的褶皱基底早已发现尖山、坪河、庙坪等中—大型、超大型石墨矿;但是直到最近,才在下层的结晶基底后河岩群汪家坪岩组细粒石英岩中发现了石墨矿。该矿体长约200米,宽约6.7米,矿体平均厚度4.9米,矿石平均品位5.13%。矿物组合为:石英+石墨+云母+黄铁矿+赤铁矿。该成果在上扬子北缘地区的发现,扩大了该区域的找矿前景,为区内晶质石墨矿的找矿工作提供了新的方向,同时为四川巴中地区超大型晶质石墨矿基地建设提供了新的资源潜力保障。数据集包括Excel表格数据,2个*.xls类型文件,记录了样品固定碳测试结果和氧化物测试数据。

A review of the synthesis and application of zeolites from coal-based solid wastes

Zeolite derived from coal-based solid wastes(coal gangue and coal fly ash)can overcome the environmental problems caused by coal-based solid wastes and achieve valuable utilization.In this paper,the physicochemical properties of coal gangue and coal fly ash are introduced.The mechanism and application characteristics of the pretreatment processes for zeolite synthesis from coal-based solid wastes are also introduced.The synthesis processes of coal-based solid waste zeolite and their advantages and disadvantages are summarized.Furthermore,the application characteristics of various coal-based solid waste zeolites and their common application fields are illustrated.Finally,we propose an alkaline fusion-assisted supercritical hydrothermal crystallization as an efficient method for synthesizing coal-based solid waste zeolites.In addition,more attention should be given to the recycling of alkaline waste liquid and the application of coal-based solid waste zeolites in the field of volatile organic compound adsorption removal.

Single-atomic Pt sites anchored on defective Ti0_(2) nanosheets as a superior photocatalyst for hydrogen evolution

Single-atomic site catalysts have drawn considerable attention because of their maximum atom-utilization efficiency and excellent catalytic activity.In this work,a highly active single-atomic Pt site photocatalyst was synthesized through employing defective Ti0_(2) nanosheets as solid support for photo-catalytic water splitting.It indicated that the surface oxygen vacancies on defective Ti0_(2) nanosheets could effectively stabilize the single-atomic Pt sites through constructing a three-center Ti-Pt-Ti structure.The Ti-Pt-Ti structure can hold the stability of isolated single-atomic Pt sites and facilitate the separation and transfer of photoinduced charge carriers,thereby greatly improving the photocatalytic H2 evolution.Notably,our synthesized photocatalyst exhibited a remarkably enhanced H2 evolution performance,and the H2 production rate is up to 13460.7μmol h^(-1)·g^(-1),which is up to around 29.0 and 4.7 times higher than those of Ti0_(2) nanosheets and Pt nanoparticles-Ti0_(2).In addition,a plausible enhanced reaction mechanism was also proposed combining with photo-electrochemical characterizations and density functional theoiy(DFT)calculation results.Ultimately,it is believed that this work highlights the benefits of a single-site catalyst and paves the way to rationally design the highly active and stable single-atomic site photocatalysts on metal oxide support.

Enhanced visible-light-assisted peroxymonosulfate activation over MnFe_(2)O_(4) modified g-C_(3)N_(4)/diatomite composite for bisphenol A degradation

The MnFe_(2) O_(4)/g-C_(3) N_(4)/diatomite composites(Mn/G/D) were prepared via a facile precipitation-calcination method in this study.The Mn/G/D possessed higher specific surface area,lower electron-hole pairs' recombination rate,as well as wider and stronger visible light absorption capacity.Since the synergistic effect between g-C_(3 )N_(4) and MnFe_(2) O_(4),the photogene rated electron could transfer from g-C3 N4 to MnFe_(2) O_(4),which could promote the migration of electrons as well as enhance the photocatalytic activity and peroxymonosulfate(PMS) activation efficiency.Mn/G/D-5% composite displayed the excellent degradation performance of bisphenol A(BPA) with the removal efficiency of 99.9% under PMS/Vis system,which was approximately 2.47 and 63.8 times as high as that of the Mn/G/D-5%/PMS and Mn/G/D-5%/Vis system,respectively.Moreover,negative electricity derived from diatomite surface also promoted the photogenerated carriers' migration,and the degradation rate constant was around 2.4 times higher than that of MnFe_(2) O_(4)/g-C_(3) N_(4)(Mn/G).In addition,quenching experiments showed that both radical pathway(h^(+),·OH,·O_(2)^(-)and SO_(4)·^(-)) and non-radical pathway(^(1) O_(2)) were responsible for the degradation of BPA.

Functionalization of diatomite with glycine and amino silane for formaldehyde removal

Two amino-functionalized diatomite(DE)composites modified by 3-aminopropyltriethoxysilane(APTS)or glycine(GLY)(i.e.,APTS/DE and GLY/DE)were successfully synthesized via the wet chemical method for the time-and cost-efficient removal of indoor formaldehyde(HCHO).First,the optimal preparation conditions of the two composites were determined,and then their microstructures and morphologies were characterized and analyzed.Batch HCHO adsorption experiments with the two types of amino-modified DE composites were also conducted to compare their adsorption properties.Experimental results indicated that the pseudo-second-order kinetic and Langmuir isotherm models could well describe the adsorption process,and the maximum adsorption capacities of APTS/DE and GLY/DE prepared under optimal conditions at 20°C were 5.83 and 1.14 mg·g^(-1),respectively.The thermodynamic parameters of the composites indicated that the adsorption process was spontaneous and exothermic.The abundant amine groups grafted on the surface of DE were derived from the Schiff base reaction and were essential for the high-efficient adsorption performance toward HCHO.

New paleomagnetic evidences of paleogene tectonic rotation of the Qaidam Basin and adjacent region: mechanism and its tectonic implication

In order to better understand the tectonic evolution of the Qaidam Basin. The authors carried out a paleomagnetic study on 39 samples of 7 sites from Hongsanhan section, northwest Qaidam Basin. Stepwise thermo-demagnefizafion isolated a high-temperature component （HTC）, which passes the fold and reversal tests at 95 % confidence level. It suggests that the HTC should be primary. Unblocking temperature （about 685℃ ） and the experiment of isothermal remanence indicate that hematite is the mainly carrier of the remanence. A tilt-corrected mean direction is： Ds= 7.1°, Is= 38.5°, α95 = 7.4°. Corresponding to a palaeopole at, φ= 250. 1°E, λ= 72.0°N, A95 = 6.8°, Compared with the reference APWP of Eurasia, the sampling area occurred a non-significant rotation （3.4° ± 5.5°） relative to Eurasia since Eocene due to the affect of left-lateral Altyn fault, Based on the paleomagnetic results of early Cretaceous and Teritary within the Qaidam block, we can obtained the mean clockwise rotations from the samples deposited from 160 Ma to 45 Ma is 24.5° ± 9.0°, and from 38 Ma to present is - 0.5° ± 7.5° relative to present geomagnetism respectively. During the Mid Eocene （45 -38 Ma） rotation phase, there should existing an important early tectonic event in northern part of the present-day Tibetan Plateau, which probably represents one of large-scale strike-slip events of the Altyn strike-slip fault.

Hierarchical assembly of highly efficient visible-light-driven Ag/g-C_(3)N_(4)/kaolinite composite photocatalyst for the degradation of ibuprofen

A novel Ag/g-C_(3)N_(4)/kaolinite composite photocatalyst was fabricated for the first time through a two-step assembly strategy by employing in situ calcination and a photodeposition process.The synthesized Ag/g-C_(3)N_(4)/kaolinite composite reached a higher degradation rate of ibuprofen(IBP)with a reaction rate constant of 0.0113 min^(-1) at an Ag content of 7% under visible-light irradiation,which was approximately 1.87 times that of the Ag/g-C_(3)N_(4) composite.Based on the physicochemical properties,the enhanced photocatalytic activity was attributed to the stronger adsorption property,wider photoresponse range and more efficient separation and transfer of electron-hole pairs.Furthermore,the incorporation of monodispersed Ag nanoparticles onto the g-C_(3)N_(4)/kaolinite sheets provided more reactive sites for the IBP degradation.In addition,according to the EPR study and trapping experiments,it was demonstrated that holes(h^(+))should be the key reactive species.A possible pathway of IBP degradation was also proposed based on the detected intermediates.Overall,the results of this work may facilitate the design of a novel visible-light-driven photocatalyst with a high efficiency that is derived from a natural mineral for environmental remediation.

Diatomite supported nano zero valent iron with 3D network for peroxymonosulfate activation in efficient degradation of bisphenol A

Diatomite supported nano zero valent iron(n ZVI)catalyst(NDA)with complex network structure was prepared via a mild reduction precipitation method in this work.The pore structure and pore distribution of NDA can be regulated and controlled through adjusting the loading amount of n ZVI.In general,the nano three-dimensional network formed by n ZVI and diatomite channels greatly increase the specific surface area and pore volume of NDA,and further formed more active sites,which made NDA have better performance in activating PMS to degrade BPA than pure n ZVI.The pseudo-first-order reaction rate constant of 50-NDA(50%-n ZVI/diatomite)is almost 3 times higher than that of pure n ZVI.Besides,the electron paramagnetic resonance(EPR)and radical quenching experiments showed that the activation process was dominated by the sulfate radical(SO_(4)^(-))and hydroxyl radical(·OH)produced by Fe;oxidation.The generated electrons promote the self-decomposition of PMS to produce singlet oxygen(^(1)O_(2)),and then the valence state of iron changes to produce free radicals.In addition,the possible degradation pathway of BPA was inferred from the intermediate products identified by liquid chromatograph-mass spectrometer(LC-MS).This study provides a novel strategy for the design and preparation of three-dimensional composite catalysts derived from natural mineral.

Synthesis of a novel illite@carbon nanocomposite adsorbent for removal of Cr(Ⅵ)from wastewater

A novel illite@carbon（I@C） nanocomposite adsorbent has been synthesized via a facile hydrothermal carbonization process（HTC） using glucose as carbonaceous source and illite as the carrier.The morphology,microstructure and surface properties of the prepared nanocomposite adsorbent were analyzed by FESEM,TGA,XRD,FT-IR and Zeta potential measurements.Batch experiments were carried out on the adsorption of Cr（Ⅵ） to determine the adsorption properties of the composite.The adsorption of Cr（Ⅵ） onto the I@C nanocomposite was well described by the pseudo-second-order kinetic model and Langmuir isotherm.Compared with the illite and carbon material（SC） separately,the prepared I@C nanocomposite adsorbent exhibited enhanced adsorption performance for Cr（Ⅵ） with a maximum adsorption capacity of 149.25 mg/g,which was higher than that of most reported adsorbents.In addition,the adsorption process was spontaneous and endothermic based on the adsorption thermodynamics study.The adsorption of Cr（Ⅵ） by I@C was highly p H-dependent and the optimum adsorption occurred at p H 2.0.The Zeta potential analysis results indicated that the electrostatic interactions between anionic Cr（Ⅵ） and the positively charged surface of the adsorbent might be critical to the adsorption mechanism.This study demonstrated that the I@C nanocomposite should be a promising candidate for a low-cost,environmental friendly and highly efficient adsorbent for the removal of toxic Cr（Ⅵ） from wastewater.

One-step synthesis of hierarchically porous hybrid TiO2 hollow spheres with high photocatalytic activity

Hierarchically porous hybrid TiO2 hollow spheres were solvothermally synthesized successfully by using tetrabutyl titanate as titanium precursor and hydrated metal sulfates as soft templates. The as-prepared TiO2 spheres with hierarchically pore structures and high specific surface area and pore volume consisted of highly crystallized anatase TiO2 nanocrystals hybridized with a small amount of metal oxide from the hydrated sulfate. The proposed hydrated-sulfate assisted solvothermal （HAS） synthesis strategy was demonstrated to be widely applicable to various systems. Evaluation of the hybrid TiO2 hollow spheres for the photo-decomposition of methyl orange （MO） under visible-light irradiation revealed that they exhibited excellent photocatalytic activity and durability.