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JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY · 2015 ·Vol. 91 ·期 4 ·985-993 · IF 2.349

Role of Mg in mesoporous MgFe2O4 for efficient catalytic ozonation of Acid Orange II

Jiang Lu,Xiaodan Wei,Yu Chang,Shuanghong Tian,Ya Xiong

BACKGROUND An ozonation catalyst needs to be recycled easily and to exhibit high activity in view of its practical application in wastewater treatment. In this study, magnetic mesoporous MgFe 2 O 4 was successfully prepared and used as a new ozonation catalyst for degradation of Acid Orange II (AOII). The role of Mg in MgFe 2 O 4 was revealed to explain the high activity by catalytic experiments and XPS analysis. RESULTS The degradation efficiency of AOII in the MgFe 2 O 4 /O 3 process exceeds 90% over a wide pH range of 4.6–9.6, slightly affected by the solution pH. The catalytic activity of MgFe 2 O 4 is much higher than that of MgO, Fe 2 O 3 and also their mixture (MgO+Fe 2 O 3 ) with identical molar ratio of Mg 2+ to Fe 3+ , indicating the first role of Mg, i.e. coupling with Fe to present a synergistically catalytic effect. Furthermore, MgFe 2 O 4 possesses a reaction rate constant at least 2.3 times that of NiFe 2 O 4 , MnFe 2 O 4 , and CuFe 2 O 4 . It illustrates the second role of Mg, i.e. causing the high electron density on lattice oxygen in MgFe 2 O 4 indicated by XPS and thus favoring activation of the electrophilic ozone. CONCLUSIONS This study demonstrated the easy recycling and high activity of MgFe 2 O 4 in catalytic ozonation, and revealed the role of Mg in MgFe 2 O 4 . © 2015 Society of Chemical Industry

研究领域: 环境科学 · 催化材料
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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

Strong degradation of orange II by activation of peroxymonosulfate using combination of ferrous ion and zero-valent copper

Xin Liu,Peng Xu,Qi Fu,Runhan Li,Chenxi He,Wenxuan Yao,Lei Wang,Shiqi Xie,Zhiyi Xie,Jingwei Ma,Qiulai He,John C. Crittenden

Zero-valent copper activated peroxymonosulfate (ZVC/PMS) system was widely used to degrade refractory contaminants due to being highly effective. However, the low reactivity and easy dismutation of cuprous species (Cu(I)) in acid condition limited its efficiency. In our study, ZVC coupled with ferrous ion (Fe(II)) promoted PMS to degrade orange II. Multiple oxidants including Cu(III), OH and SO 4 − made main contribution on orange II degradation in the Fe(II)/ZVC/PMS system. In the Fe(II)/ZVC/PMS system, ZVC generated Cu(I) by H + corrosion and PMS oxidation, and Cu(I) reacted with oxygen producing hydrogen peroxide. Then, Fe(II) and Cu(I) catalyzed hydrogen peroxide and PMS to generate Cu(III), OH and SO 4 − , and thereinto Fe(III) was reduced to Fe(II) by ZVC and Cu(I). In the Fe(II)/ZVC/PMS system, water matrix including humic acid, sulfate and nitrate had no significant impact on orange II degradation, while chloride restrained the degradation of orange II. The Fe(II)/ZVC/PMS system exhibited great degradation for orange II in tap water, lake water and well water. Additionally, the Fe(II)/ZVC/PMS system degraded more than 90% of methyl orange, rhodamine B, acetaminophen, ibuprofen, propranolol and diclofenac. Through adjusting the final reaction solution to pH 8.5 and subsiding, the discharge of total copper met the II-level environmental quality standards for surface water in China (1 mg/L). Hence, the study provided a promising method to induce PMS for enhanced degradation of contaminants.

研究领域: 环境科学 · 化学工程
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Journal of Cleaner Production · 2017 · IF 5.715

Producing sawdust derived activated carbon by co-calcinations with limestone for enhanced Acid Orange II adsorption

Lingjun Kong,Minhua Su,Yan Peng,Li'an Hou,Juan Liu,Haipeng Li,Zenghui Diao,Kaimin Shih,Ya Xiong,Diyun Chen

Because of the widespread application of activated carbon (AC) as adsorbents, reduced production costs are highly desirable, therefore, inexpensive alternatives for activated carbon precursors and eco-procedures are presently sought. In this work, AC was successfully prepared from sawdust through co-calcinations with limestone. The surface area and porosity of the resulting ACs were evaluated according to the N 2 adsorption at 77 K. Acid Orange II (AOII) was utilized as a negative dye to study the potential of the resulting AC as an adsorbent. Results revealed that the surface area and total pore volume were both increased greatly. When the activated carbon was prepared in mass ratios of 1:2 and 1:1 (calcium carbonate to sawdust), the surface area increased to 611.4 and 706.9 m 2 /g, respectively, and the adsorption capacities increased to 310.89 and 389 mg/g. These enhancements indicated efficient activation, resulting in energy-saving and environmentally friendly activated carbon production. Thus, this paper provides a cleaner process for producing activated carbon from waste sawdust through bioresource recycling.

CAS / MDL: 471-34-1
研究领域: 环境科学 · 材料科学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2022 ·Vol. 33 ·期 29 ·23187-23195 · IF 2.779

Preparation of stone-shaped CuBi2O4 by solid phase method and H2O2 assisted visible light degradation for orange II

Yi Junhui,Li Minghao,Xie Runkun,Liao Xiaoying,You Jinfeng,Chen Beifang,Liu Qiqi,Huang Weili

CuBi 2 O 4 is widely used in photocatalytic degradation for pollutants in water due to its strong visible light response characteristics, excellent chemical stability, non-toxic, and low cost. Here, stone-shaped CuBi 2 O 4 was prepared with CuO and Bi 2 O 3 as raw materials by high temperature solid phase. The effect of calcined temperature and time on the product was discussed. This material was analyzed and discussed by XRD, SEM, XPS, and DRS, and the visible light activity of degradation for Orange II was explored. The results showed that the absorption edge of prepared CuBi 2 O 4 expands to the visible region, and the band gap was about 1.77 eV. The photocatalytic degradation rate of Orange II was 42.6% under the optimal conditions. After H 2 O 2 assisted, the degradation rate was more than 2 times, and repeated experiments verified that the prepared catalysts had high stability. Finally, a reasonable mechanism of H 2 O 2 assisted degradation enhancement is proposed. This work gives new ideas for the preparation of new and efficient catalytic materials.

研究领域: 材料科学 · 环境科学
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2022 ·Vol. 29 ·期 48 ·73353-73364 · IF 5.19

Activating peroxymonosulfate using carbon from cyanobacteria as support for zero-valent iron

Chen Jun,Zhu Layun,Cao Sisi,Song Zihui,Yang Xiaohong,Jin Jie,Chen Zhaoming

In the present study, the cyanobacterial char (ACC) prepared from Chaohu cyanobacteria was used as a nanoscale carrier for zero-valent iron (NZVI) to synthesize a highly efficient activation material designated as cyanobacterial char-supported nanoscale zero-valent iron (NZVI@ACC), which was subsequently used for activating peroxymonosulfate (PMS) to degrade the orange II (OII) dye. The XRD and XPS results revealed that NZVI was anchored onto the ACC through coordination bonding, forming a stable structure. The SEM and TEM observations revealed that the NZVI was embedded in the sheet structure of the ACC. The NZVI@ACC had a larger specific surface area (42.249 m 2 /g) and also magnetism, due to which its components could be separated through an externally applied magnetic field. Using this NZVI@ACC/PMS system, the rate of degradation of OII (100 mg/L) reached 98.32% within 14 min. The OII degradation reaction using the NZVI@ACC/PMS system followed first-order kinetics. The activation energy of this degradation reaction was 17.34 kJ/(mol·K). Quenching and EPR experiments revealed that various free radicals (SO 4 · − , ·OH) were produced, with SO 4 · − playing the major role in the reaction. The theoretical calculations revealed that SO 4 · − attacked the 12 (N) of OII, thereby destroying and degrading both azo and hydrogenated azo structures of OII. The presence of halogen ions in the actual dye-containing wastewater samples inhibited the OII degradation by the NZVI@ACC system to different degrees, and the inhibition effect followed the order I −  > Br −  > Cl − .

研究领域: 环境科学 · 材料科学
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Separations · 2025 ·Vol. 12 ·期 4 ·101 · IF 2.7

Degradation of Acid Orange II by FeOCl/Biochar-Catalyzed Heterogeneous Fenton Oxidation

Jiren Yuan,Dongao Xie,Dan Li,Feigao Xu

In recent years, the rapid development of industry has led to the discharge of large quantities of pollutants, including harmful dyes, into water sources, thereby posing potential threats to human health and the environment. FeOCl and biochar have their own shortcomings as a mediator in the heterogeneous Fenton process. To make both materials useful, FeOCl supported on bamboo biochar (FeOCl/BC) was prepared by calcination using FeCl3·6H2O and bamboo powder as raw materials, and the composite’s catalytic activities were explored with acid orange II (AO-II) as the target pollutant. The degradation efficiency of FeOCl/BC composites on AO-II was determined by testing the mass ratio of FeOCl and BC, initial pH, temperature, H2O2concentration, catalyst addition, addition of coexisting inorganic anions, and natural organic matter. The addition of biochar to FeOCl increased the activation of H2O2to generate •OH for the removal of AO-II and accelerated the cycle of Fe3+/Fe2+. The removal rate of AO-II by the Fe1C0.2composite was 97.1% when the mass ratio of FeOCl and BC was 1:0.2 (Fe1C0.2), which was higher than that of the pure components (FeOCl or BC) at pH = 6.1. Moreover, after five reuses, the Fe1C0.2composite still showed high degradation activity for AO-II, with 83.3% degradation and low activity loss. The capture experiments on the active material showed that the removal of AO-II by the Fe1C0.2composite was mainly dominated by •OH; however, •O2−andh+played minor roles. The synthesized Fe1C0.2composite could be applied for organic contaminants such as AO-II with high removal efficiency.

研究领域: 环境科学 · 材料科学 · 化学工程
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CERAMICS INTERNATIONAL · 2020 · IF 3.83

Ionic liquid-assisted synthesis of hierarchically olive-like Al2O3 and CeO2/Al2O3 with enhanced catalytic activity for Orange II degradation

Xiaoyu Yang,Xuanxuan Lei,Shaokun Tang

A simple hydrothermal method is utilized to fabricate hierarchically olive-like γ -Al 2 O 3 using ionic liquid [Bmim]BF 4 as the structure directing agent . The olive-like γ -Al 2 O 3 presents uniform morphology with the average diameter of 500 nm and rich mesopores. As template, ionic liquid [Bmim]BF 4 plays a crucial role in the controllable morphology of the product. [Bmim]BF 4 is absorbed on the AlOOH nanoparticles surface via the H-bond interaction and induces crystalline oriented growth. Then the forming AlOOH nanosheets self-assemble into olive-like hierarchical structure through π–π stack interaction. Given that the structure advantage of the olive-like γ-Al 2 O 3 and the limited study concerning cerium-based catalysts in Fenton-like reaction, nano-CeO 2 / γ -Al 2 O 3 supported catalyst is prepared and used in Fenton-like degradation for the first time. The result suggests that the olive-like γ -Al 2 O 3 support not only reduces the surface energy with more uniform CeO 2 (ca. 4–5 nm) dispersion but also improve the concentration of Ce 3+ active sites. The CeO 2 / γ -Al 2 O 3 catalyst displays superior catalytic activity for the degradation of Orange II (AO7) compared with pure CeO 2 nanoparticles.

CAS / MDL: 109-73-9 7722-84-1
研究领域: 材料科学 · 环境科学 · 催化化学
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CELLULOSE · 2019 ·Vol. 26 ·期 5 ·3285-3297 · IF 3.917

Removal of chromium(VI) and orange II from aqueous solution using magnetic polyetherimide/sugarcane bagasse

Gao Hejun,Du Jia,Liao Yunwen

Abstract A novel biological magnetic adsorbent was successfully constituted with sugarcane bagasse (SCB), polyetherimide (PEI) and Fe 3 O 4 . The physicochemical properties of the adsorbent (Fe 3 O 4 @PEI/SCB) were investigated by SEM, BET, VSM, XRD, TGA, FT-IR, XPS, TEM and UV–Vis. The adsorption capacity was measured using Cr(VI) and orange II as adsorbates. The effects of initial pH, dosage, contact time, and ionic strength on the adsorption capacity were investigated in detail. Fe 3 O 4 @PEI/SCB is a mesoporous material and the mass ratio of Fe 3 O 4 :PEI:SCB is about 5:2:15. Adsorption capacity could reach 182.28 mg/g and 1893.57 mg/g for Cr(VI) and orange II at room temperature, respectively. Fe 3 O 4 @PEI/SCB is a green and economical material, which is very easily regenerated, reused, and separated in the adsorption. The most important factor is the ionic strength and major adsorption interaction was electrostatic in this work. Graphical abstract

研究领域: 环境科学 · 材料科学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2022 · IF 5.518

Persulfate activation of CuS@Ti3C2-based MXene with Bi-active centers toward Orange II removal under visible light

Qi Wang,Yu Mei,Ruoxue Zhou,Sridhar Komarneni,Jianfeng Ma

The Ti 3 C 2 -based MXene with unique lamellar nanostructure and high conductivity is expected to effectively improve photocatalytic ability of composites as a cocatalyst. Herein, two dimensional Ti 3 C 2 -based MXene nanosheets decorated with copper sulfide particles (CuS@MXene) were synthesized by hydrothermal treatment to boost catalytic persulfate (PS) activation under light, exhibiting remarkable reactivity and stability for the rapid removal of Orange II. The phase composition of CuS@MXene was detected by X-ray diffraction (XRD), the morphology of CuS@MXene was characterized by scanning electron microscope (SEM), and the results of X-ray photoelectron spectroscopy (XPS) proved the elemental composition and valence state of elements in the CuS@MXene. The dosage of PS and initial pH of solution were the main factors affecting the removal rate of Orange II, and the quenching experiment showed that 1 O 2 was the primary reactive species for the removal of Orange II in CuS@MXene -PS system. In addition, this study showed that CuS@MXene provided bi-active centers for PS activation, which was mainly attributed to the rapid charge transfer between dual electron-rich active centers of Cu and Ti. This system may be applicable to the degradation of other challenging organic pollutants .

研究领域: 环境科学 · 材料科学
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JOURNAL OF SEPARATION SCIENCE · 2013 · IF 2.591

Preparation and evaluation of a novel molecularly imprinted SPE monolithic capillary column for the determination of auramine O in shrimp

Jiangmei Li,Haiyun Zhai,Zuanguang Chen,Qing Zhou,Zhenping Liu,Zihao Su

A novel method combining molecular imprinting and SPE was developed in a capillary column for the determination of auramine O in shrimp. The capillary monolithic column was prepared by UV-initiated in situ polymerization, using auramine O as template and methacrylic acid and ethylene dimethacrylate as functional monomer and cross-linker, respectively. The properties of the prepared capillary monolithic column were investigated under the optimized conditions coupled with HPLC, and then the morphologies of the inner polymers were characterized by SEM. The calibration curve was expressed as A = 103 C + 19.8 ( r = 0.9992) with a linear range of 0.25–25.0 μg/mL, and the recoveries of auramine O at different concentrations in shrimp ranged from 90.5 to 92.4% with RSDs ranging from 2.1 to 4.4%. The capacities of the molecularly imprinted polymer and nonimprinted polymer columns were 0.722 and 0.147 μg/mg, respectively, and the LOD (S/N = 3) of auramine O in shrimp was 17.85 μg/kg. Under the selected conditions, the enrichment factors obtained were higher than 70-fold. The results indicate that the prepared molecularly imprinted capillary monolithic column was reliable and applicable to the analysis of auramine O in shrimp.

研究领域: 分析化学 · 食品安全
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CHEMOSPHERE · 2021 · IF 7.086

Visible-light-driven activation of sodium persulfate for accelerating orange II degradation using ZnMn2O4 photocatalyst

Fang Zhu,Jianfeng Ma,Qiuyue Ji,Hao Cheng,Sridhar Komarneni

A special catalytic system was obtained by using ZnMn 2 O 4 (ZMO) materials to activate Na 2 S 2 O 8 and catalytically degrade organic dye orange II under visible light irradiation. The ZMO nanoparticles were prepared by a simple one-step method and characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and ultraviolet–visible diffuse reflectance spectroscopy (UV–Vis DRS). In this study, the ZMO/Na 2 S 2 O 8 system was used to degrade orange II, and the degradation rate reached 97.44% in 60 min. ZMO catalysts could be recycled for at least five times, and its degradation rate was only decreased by 1.84%. The free radicals produced during the degradation of orange II were studied by classical quenching experiments, and the different types of free radicals produced in the system were further confirmed by electron paramagnetic resonance (EPR) spectroscopy. The catalytic degradation of orange II in this system was mainly caused by the production of superoxide , sulfate and hydroxyl radicals, which achieved high degradation.

研究领域: 环境科学 · 催化化学
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2017 · IF 3.671

Adsorption of Cr(VI) on cerium immobilized cross-linked chitosan composite in single system and coexisted with Orange II in binary system

Tianyi Zhu,Wei Huang,Lingfan Zhang,Jie Gao,Wenqing Zhang

In this work, cerium immobilized cross-linked chitosan (CTS-Ce) composite, employed as an efficient adsorbent for Cr(VI) in single system and coexisted with Orange II (OII) in binary system, was prepared by co-precipitation method. The as-obtained adsorbent was characterized by FTIR, SEM, EDS and XPS before and after adsorption. The adsorption behaviors of Cr(VI) in single and binary system were systematically studied. The maximum adsorption capacity of Cr(VI) on CTS-Ce (202.8   mg/g) was calculated by Langmuir equation in single metal system, but it decreased to 112.9   mg/g with initial concentration of 100   mg/L OII in binary system at pH 2 and 293   K. The adsorption data for Cr(VI) followed the Langmuir model in single system, while fitted Temkin model well in binary system. In both single and binary system, the kinetics of adsorption exhibited pseudo-second order behavior and adsorption capacity increased with increasing temperature. Moreover, the data of thermodynamic parameters ( ΔG°   <   0, ΔH°   >   0) indicated that the adsorption was a spontaneous and endothermic process. Besides, | Δ G C r | > | Δ G C r − O I I | at the same temperature further suggested that Cr(VI) was adsorbed on the CTS-Ce composite faster in binary system than in single system.

研究领域: 环境科学 · 材料科学
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