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Surfaces and Interfaces · 2023 · IF 6.2

Superior photocatalytic performance of ancillary-oxidant-free novel starch supported nano MFe2O4 (M = Zn, Ni, and Fe) ferrites for degradation of organic dye pollutants

A.V. Ravindra,M. Chandrika,Andem Sandeep

This work presents the effectual degradation of MB and MO dyes in an aqueous solution under UV light irradiation on nano ZnFe 2 O 4 , NiFe 2 O 4 , and Fe 3 O 4 without using any supplementary oxidants has been reported. Nano ZnFe 2 O 4 , NiFe 2 O 4 , and Fe 3 O 4 are successfully prepared via a co-precipitation technique utilizing biodegradable starch as a surfactant . XRD patterns reveal a pure spinel phase for all the samples. FTIR spectra confirm the successful embedding of the starch surfactant. SEM micrographs exhibit tiny spherical particles of size 5–8 and 4–6 nm for ZnFe 2 O 4 and NiFe 2 O 4 but spherical particles of 8–10 nm and flake-like particles of ∼14 nm thick for Fe 3 O 4 . N 2 sorption studies show type-IV isotherms typical of mesoporous structures. The direct bandgap of these ferrite nanoparticles is 2.03–2.15 eV, related to the metal D-d onsite transfers, which are permitted by spin but prohibited by parity. MB decolorization of 99% is achieved in less than 2 h for all the samples; in contrast, MO decolorization takes relatively longer irradiation. The decolorization kinetics suggests that the pseudo-second-order model is more appropriate to explain the decolorization process of MB and MO by the catalysts. The order of photocatalytic activity evaluated from rate constant (k 1 ) per SSA values is Fe 3 O 4 < ZnFe 2 O 4 < NiFe 2 O 4 for both MB and MO decolorization. NiFe 2 O 4 photocatalyst shows the best effect on the decolorization of both dyes due to its low bandgap and high surface area. All the ferrite catalysts demonstrate high stability with no substantial deterioration of photocatalytic activity even after three cycles. The results of this study endorse that the nano ferrites prepared in this work are potential candidates for the photocatalytic degradation of aqueous solutions of MB and MO.

研究领域: 环境科学 · 材料科学 · 化学
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ADVANCED FUNCTIONAL MATERIALS · 2025 · IF 19

Type-II Heterojunction Regulated BIEF Toward Nitride/Chalcogenide Semiconductors for Multi-Polarization Relaxation

Mengjia Shi,Zirui Jia,Di Lan,Zhenguo Gao,Siyuan Zhang,Guanglei Wu

Designing and constructing built-in electric field (BIEF) between substances is an effective way to enhance multi-polarization relaxation. Ni 3 S 4 @Co 4 S 3 /Ni 3 N@Co 2 N 0.67 (NC-S/NC-N) composites are prepared through multiple hydrothermal and nitriding steps. The influence of the BIEF constructed by the Type-II heterojunction between the corresponding substances on the wave absorption performance is investigated. A BIEF model is constructed for this material, and the transfer mechanism of electrons and holes in the BIEF is studied. The crystal structure, lattice parameters, unit cell volume, and phase composition of composites are quantitatively analyzed by XRD refinement using the Rietveld method. The electronic structure of the heterointerface is studied by using density functional theory (DFT) calculations to verify the characteristics of Type-II heterojunctions and the formation of BIEF. The BIEF constructed by Type-II heterojunction enhances the interfacial polarization intensity by regulating the interfacial charge distribution, accelerates carrier transport, and increases conductive loss. It also affects magnetic loss by modulating the spin polarization of Ni/Co magnetic components. When the matching thickness is 2.1 mm, the minimum reflection loss (RL min ) can reach −51.64 dB. Meanwhile, the maximum effective absorption bandwidth (EAB max ) can cover 5.12 GHz at 2.3 mm. The results show that the microscopic interface mechanisms provides a brand-new path.

CAS / MDL: 64-17-5 67-56-1 68-12-2
研究领域: 材料科学 · 凝聚态物理 · 电磁功能材料 · 纳米复合材料 · 能量存储与转换
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RSC Advances · 2016 ·Vol. 6 ·期 86 ·82707-82715 · IF 3.289

The enhanced performance of a CeSiOx support on a Mn/CeSiOx catalyst for selective catalytic reduction of NOx with NH3

Wei Li,Rui-tang Guo,Shu-xian Wang,Wei-guo Pan,Qi-lin Chen,Ming-yuan Li,Peng Sun,Shu-ming Liu

A series of Mn/CeSiOx catalysts were prepared by the wet impregnation method and used for selective catalytic reduction of NO with NH3. As can be seen from the experimental results, the Mn/CeSiOx catalyst with a Ce/Si molar ratio of 2/1 showed excellent low-temperature SCR activity, high N2 selectivity and excellent SO2 and H2O tolerance. The relationship between the CeSiOx support and the SCR performance of Mn/CeSiOx (2 : 1) catalyst was investigated based on the characterization results of N2 adsorption, XRD, XPS, H2-TPR, NH3-TPD and in situ DRIFT. The strong interaction between Ce and Si resulted in the good dispersion of Mn species on the support; correspondingly, the redox ability and NH3 adsorption capacity were greatly enhanced. The results of in situ DRIFT study revealed that the NH3-SCR reactions over Mn/CeO2 and Mn/CeSiOx (2 : 1) mainly obeyed both the E–R mechanism and the L–H mechanism. Furthermore, the formation of more Mn4+ and chemisorbed oxygen greatly facilitates the oxidation of NO to NO2, as a result, promoting the low-temperature SCR performance of Mn/CeSiOx (2 : 1).

研究领域: 催化 · 环境科学 · 化工
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JOURNAL OF THE CERAMIC SOCIETY OF JAPAN · 2015 ·Vol. 123 ·期 1441 ·719-724 · IF 0.698

Novel hybrid luminescent materials derived from multicarboxy cage silsesquioxanes and terbium ion

Liguo LI,Shengyu FENG,Hongzhi LIU

Multicarboxy (8, 16) functionalized cage silsesquioxanes were synthesized through the photochemical thiol-ene reaction of octavinylsilsesquioxane with 3-mercaptopropionic acid and mercaptosuccinic acid, respectively. These two cage precursors acted as ligands to coordinate with terbium ion (Tb3+) to obtain two novel hybrid luminescent materials, which exhibited fine luminescent properties and good thermal stabilities. Their morphologies were investigated by XRD, SAXS, SEM, TEM and DLS. And the results showed that self-assembly particle size of the hybrid complex with octacarboxyl cage was larger size than that of cage with 16 carboxyl groups.

研究领域: 材料科学 · 化学 · 纳米技术
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TALANTA · 2024 · IF 5.6

Magnetic biochar prepared from a spent mushroom substrate as an adsorbent for the analysis of pyrethroids in environmental water samples

Wenfei Zhao,Wen Wang,Yixuan Wu,Wenhui Guo,Wenzhuo Ren,Shiyu Meng,Shaojun Yun,Cuiping Feng

In this study, a spent mushroom substrate (SMS) from Lentinus edodes cultivation was used to prepare biochar (BC) and magnetic biochar (MBC) at high temperatures. The magnetic field strength of MBC was proved via VSM analysis. The results of the nitrogen adsorption‒desorption isotherms of BC and MBC showed that MBC exhibited stronger adsorption, and SEM was performed to compare the microstructures of BC and MBC. TEM was performed to compare the distributions of C, O, and Fe. The FT-IR and XRD results revealed changes in the structure and the formation of new substances after magnetization; that is, MBC was more conducive to the adsorption and recovery of pesticides. Moreover, a method for the detection of tetramethrin, beta-cypermethrin, and fenvalerate in water samples (tap water, lake water, and river water) was established, and this method combined the use of MBC as adsorbent and high-performance liquid chromatography. Moreover, great linearity of the method was obtained in the range of 0.5–2.5 μg/mL; the recoveries in real samples were in the range of 70.20–73.32%, and the RSDs were in the range of 0.22–1.09%. The method is simple and effective, is suitable for the detection of pyrethroids in water, and has certain application potential.

研究领域: 环境科学 · 分析化学 · 材料科学 · 农业科学
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2019 · IF 4.084

Catalytic characteristics of innovative Ni/slag catalysts for syngas production and tar removal from biomass pyrolysis

Yang Liu,Haimiao Yu,Jiecheng Liu,Dezhen Chen

In this study, innovative Ni-based catalysts supported by five typical slag carriers (magnesium slag (MS), steel slag (SS), blast furnace slag (BFS), pyrite cinder (PyC) and calcium silicate slag (CSS)) were prepared by wet impregnation. With the prepared catalysts and Ni/γ-Al 2 O 3 catalyst, catalytic reforming of pyrolysis volatiles from pine sawdust for syngas production and tar removal was investigated. The catalysts were characterized by BET, XRD , SEM, TEM and Raman. The catalytic performances of the six catalysts were decreasing in the following order: Ni/MS > Ni/γ-Al 2 O 3  > Ni/SS > Ni/BFS > Ni/CSS > Ni/PyC. Ni/MS catalyst exhibited excellent catalytic reactivity as well as thermal stability in terms of tar conversion (95.19%), gas yield (1.46 Nm 3 /kg) and CO 2 capture ability (CO 2 yield of 0.5%). Both amorphous carbon and graphite-type carbon were formed on the catalysts after catalytic reforming and the D/G ratio (the relative intensity ratio of the D-band to the G-band) was positively correlated to the catalytic activity .

CAS / MDL: 13478-00-7
研究领域: 催化 · 化学工程 · 环境科学 · 材料科学
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2019 ·Vol. 26 ·期 28 ·28860-28870 · IF 2.914

Design and synthesis of organic rectorite-based composite nanofiber membrane with enhanced adsorption performance for bisphenol A

Sun Zhiming,Yuan Fang,Zhang Xinchao,Zhu Rui,Shen Xinyi,Sun Bingyan,Wang Bin

Nowadays, most of mineral-based adsorbents are powder form, which makes them inconvenient to collect and always easy to cause secondary pollution. In this work, an organic rectorite composite nanofiber membrane (SRt-PAN) was designed and prepared by electrospinning technique. The as-received composite nanofiber membranes were characterized by XRD and SEM analysis, proving the homodisperse and existence of SRt in PAN nanofiber membrane. A series of batch experiments for BPA adsorption were carried out to investigate the effect of different adsorption parameters, including initial concentration, pH, and temperature of pollutant solution. The influences of modifier dosage and adsorbent dosage on the adsorption performance were investigated as well. On the basis of the experiment results, the adsorption process could be well described by the pseudo-second-order model and the Langmuir isotherm. In addition, the thermodynamic parameters indicate that this adsorption process is exothermic and spontaneous. Moreover, compared with pure nanofiber membranes and organic rectorite powders, the resultant SRt-PAN adsorbents exhibited higher adsorption capacity, superior reusability, and adsorption stability. It is indicated that the hydrophobicity surface of organic rectorite should be the key factor to not only the intimate interfacial combination between the mineral and PAN, but also the enhancement of BPA adsorption capacity.

CAS / MDL: 80-05-7 1120-02-1
研究领域: 材料科学 · 环境工程 · 化学工程
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2021 · IF 6.953

Ninhydrin-functionalized chitosan for selective removal of Pb(II) ions: Characterization and adsorption performance

Yingbi Chen,Jiali Tang,Shixing Wang,Libo Zhang

A chitosan-based adsorbents (CS-Ninhydrin) was prepared by grafting ninhydrin for Pb(II) ions adsorption. SEM-EDS, XRD and FTIR analysis were used to characterize the synthesized CS-Ninhydrin. The static adsorption experiments showed that CS-Ninhydrin had a good removal rate for Pb(II) ions in a wide range of pH 3 to 7, quickly reached equilibrium (120 min) and had a higher adsorption capacity (196 mg/g). Pseudo second-order and Langmuir models showed that the adsorption process of Pb(II) by CS-Ninhydrin was a single-layer chemical adsorption. Temperature experiments showed that the reaction was a spontaneous exothermic process. In the wastewater experiment, CS-Ninhydrin showed an excellent selectivity to Pb(II) ions. The reusability of CS-Ninhydrin was perfect after five adsorption-desorption cycles. The main adsorption mechanism was the chelating and electrostatic action between N and O groups in CS-Ninhydrin and Pb(II) ions. Therefore, the new adsorbent CS-Ninhydrin was expected to promote the wide application of chitosan in Pb(II) adsorption.

CAS / MDL: 485-47-2
研究领域: 环境科学 · 材料科学 · 化学工程
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2021 · IF 4.539

Self-assembled Au/Fe3O4 nanoparticle-loaded phytic acid-graphene oxide composite foam with highly efficient catalytic performance for p-nitrophenol and o-nitroaniline organic pollutants

Ran Wang,Chong Cai,Di Wang,Zhiwei Liu,Lili Gao,Tifeng Jiao

In this work, a new type of self-assembled phytic acid-graphene oxide composite foam (PAGF) was prepared by hydrothermal method. In addition, Au nanoparticles (Au NPs) and Fe 3 O 4 particles were loaded onto PADF to obtain PAGF@Au&Fe 3 O 4 composite by a simple one-step method. The addition of graphene oxide (GO) can effectively prevent the agglomeration of Au NPs and weaken its surface passivation. The results of SEM, XRD, XPS and BET proved the successful preparation of the composite and its large specific surface area. Moreover, the synthesized PAGF@Au&Fe 3 O 4 composite showed good catalytic performance for p-nitrophenol (4-NP) and o-nitroaniline (2-NA) solutions with the rate constant (k) values of 0.0799 min −1 and 0.0546 min −1 , respectively. Due to the addition of Fe 3 O 4 , the composite exhibited good stability and recyclability, and maintained high catalytic efficiency after 8 cycles of catalytic process. The current work provides new ideas for developing novel graphene oxide-based composite materials and their catalytic degradation of organic pollutants.

研究领域: 材料科学 · 环境科学 · 纳米技术 · 催化
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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Pd (II) bioreduction by Bacillus wiedmannii MSM with energy storage compounds

Yuan Chen,Yuancai Chen,Yexia Qin

In the present study, we found that nanoparticles (Pd-NPs) were biosynthesized by Bacillus wiedmannii MSM ( B. wiedmannii MSM) with endogenous carbon under O 2 condition, and more favorablity under N 2 purging condition. XRD results indicated that crystal planes of Pd-NPs were attributed to Pd 0 (111), Pd 0 (200), Pd 0 (220), and Pd 0 (311), respectively. TEM and STEM-EDX results showed that the bio-reduction of Pd (II) ( k pd,1 =4.799 min −1 ) occurred predominately in periplasm space. FTIR results showed that the -COOH, -OH, and -NH 2 were the main groups participating in the removal of Pd (II). The aerobic reduction of Pd (II) by B. wiedmannii MSM was proposed, including extracellular superoxide radicals produced by NAD(P)H oxidases , endogenous electron donors, and O 2 -insensitive hydrogenase. These studies provide new methods and insights for reduction of Pd (II).

CAS / MDL: 13820-53-6
研究领域: 环境科学 · 材料科学 · 微生物学 · 化学
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2015 ·Vol. 162 ·期 6 ·E68 · IF 3.266

Cobalt Powder Production by Electro-Reduction of Co3O4 Granules in Molten Carbonates Using an Inert Anode

Xinhua Cheng,Diyong Tang,Dingding Tang,Hua Zhu,Dihua Wang

Electrochemical splitting of Co3O4 into cobalt powder and oxygen was realized by electrolysis in molten Na2CO3-K2CO3 at 1023 K using a solid oxide pellet cathode and a Ni11Fe10Cu alloy inert anode. The electro-reduction mechanism of Co3O4 was investigated in details by cyclic voltammetry measurements and potentiostatic electrolysis in a three-electrode cell combining with the composition and morphology characterization of the electrolytic products. The electro-reduction of Co3O4 in Na2CO3-K2CO3 melt mainly involves two steps by electrochemical formation of intermediate product of CoO and then the CoO is reduced to cobalt metal. NaxCoO2 intermediate was not detected by XRD measurements and EDX analysis, different from the electro-reduction of Fe2O3 in this melt. However, the particle size and morphology of the intermediate CoO is found to be dependent of the applied potential in the range of −0.35 V to −0.75 V vs. Ag/Ag2SO4 reference electrode. Metallic cobalt powder was prepared by potentiostatic electrolysis at potential more negative than −1.25 V (vs. Ag/Ag2SO4) or by constant cell voltage electrolysis under a cell voltage higher than 1.7 V using a Ni11Fe10Cu inert anode. A high current efficiency of 95.3% and a low electrolysis energy consumption of 2.16 kW·h/kg-Co represents a novel high efficiency and green process for Co extraction. The Co product is a mixture of FCC and HCP structure, which is affected by the applied cell voltage and deserves further investigation to recognize the structure controllable condition and mechanism.

CAS / MDL: 1308-06-1
研究领域: 材料科学 · 电化学 · 冶金工程 · 能源工程
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FIBERS AND POLYMERS · 2024 ·Vol. 25 ·期 5 ·1713-1725 · IF 2.2

A Sulfonic-Functionalized Cellulose Adsorbent for the Rapid Removal of Cerium (III) from Aqueous Solutions

Tan Lei,Bai Xiuzhi,Yao Rui,Fu Zengjin,Wang Jing,Wang Yicheng,Lin Tingrui,Hao Yan,Yang Hui,Yang Huimin,Sai Huazheng

The biodegradable biomass adsorbent (cellulose- g -PSS) was synthesized in LiCl/ N, N -dimethyl acetamide by the free-radical grafting polymerization reaction between sodium styrene sulfonate (SSS) and cellulose. Systematic optimization was conducted on many reaction parameters, including reaction time, monomer dosage, and reaction temperature. The grafting yield of cellulose- g -PSS was 50.16%. The chemical structures, physical, and chemical characteristics of cellulose- g -PSS were characterized by FTIR, SEM, PZC, 1 H NMR, XRD, TGA and XPS. An assessment was conducted to determine the sorption of Ce (III) on cellulose- g -PSS by changing the contact time, adsorbent dosage, pH, initial Ce (III) concentration, and NaCl concentration. The process of adsorption rapidly reached a state of equilibrium within a time frame of 25 min and was well explained using pseudo-second-order kinetic and Langmuir isotherm model. The maximum adsorption capacity for Ce (III) obtained from the Langmuir isotherm model was 84.80 mg·g −1 . The impact of NaCl concentration on the sorption of Ce (III) and XPS analysis showed that Ce (III) ions were adsorbed onto cellulose- g -PSS through ion-exchange mechanism. As a whole, cellulose- g -PSS exhibited great potential in rare earth wastewater treatment.

CAS / MDL: 110-26-9 7727-21-1
研究领域: 环境科学 · 化学工程 · 材料科学
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