JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
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2015
·Vol. 91
·期 4
·985-993
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IF 2.349
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
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催化材料
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DOI
高影响因子
RSC Advances
·
2018
·Vol. 8
·期 8
·3934-3940
·
IF 2.936
Chunyong Zhang,Wei Chen,Jiahui Xian,Degang Fu
In this work, a novel definitive screening design (DSD) was initially used to investigate the in situ chemical oxidation of acid orange-II (AO II) dye using a homogeneous cobalt-catalyzed peroxymonosulfate (Co2+/PMS) system. Experiments were performed in a batch reactor using a synthetic AO II solution containing cobalt ions, humic acid (HA) and five electrolyte salts (NaCl, NaNO3, NaHCO3, Na2SO4 and NaH2PO4). The effects of nine operating variables on AO II degradation: NaCl concentration (0–20 mM), NaH2PO4 concentration (0–20 mM), NaHCO3 concentration (0–20 mM), NaNO3 concentration (0–20 mM), Na2SO4 concentration (0–20 mM), HA concentration (0–40 mg L−1), PMS concentration (2–10 mM), AO II concentration (0–100 mg dm−3) and Co2+ concentration (0–1.36 mM), were investigated. Analysis of a DSD model revealed that only four variables were statistically significant. Besides, our results indicated that there were no significant interactive effects between the five anions employed. Thereafter, a central composite rotatable design (CCRD) was adopted to further optimize these significant variables. A CCRD model describing AO II conversion as a function of PMS concentration, NaCl concentration and Co2+ concentration was then constructed and used to explore the final optimal operating conditions. As a consequence, the combination of DSD and CCRD allowed reducing the number of experiments from over 600 to only 39. Lastly, a plausible reaction sequence concerning the oxidation of AO II in the Co2+/PMS/Cl− system was also proposed. The route of AO II oxidation involved hydroxylation and chlorination, signifying the roles of both sulfate radicals and active chlorine species.
研究领域:
环境科学
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化学工程
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DOI
高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2023
·Vol. 30
·期 21
·59366-59381
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IF 5.8
Xiong Huixin,Shi Kun,Han Jie,Cui Can,Liu Yang,Zhang Bailin
Discharge of the untreated dye-containing wastewaters will induce water source pollution and further harm aquatic organisms. In this study, the akaganéite/polyaniline catalyst (β-FeOOH/PANI, about 1.0 μm) could be successfully composed by polyaniline (PANI, (C 6 H 7 N) n , 200–300 nm) and akaganéite (β-FeOOH, FeO(OH) 1−x Cl x , less than 200 nm), according to the identification and characterization results of XRD, Ramon, FTIR, XPS, SEAD, EDS, and FESEM (or HRTEM). Due to PANI providing more photogenerated electrons, the β-FeOOH/PANI composite (compared with β-FeOOH) in photo-Fenton system had the more highly catalytic degradation capacity to Acid Orange II (AOII) under an optimal condition (7.5 mmol/L of H 2 O 2 oxidant, 40 mg/L of AOII, 0.2 g/L of catalyst dosage, and pH 4.0). The AOII degradation kinetics could be well fitted by pseudo-first-order model. In photo-Fenton catalytic process of AOII dye, the ∙OH and h + were the main reaction substances. The AOII in solutions could be gradually mineralized into non-toxic inorganic H 2 O molecule and CO 2 . The β-FeOOH/PANI catalyst also had a good reusable ability of about 91.4% AOII degradation after 4 runs. These results can provide a reference for synthesis of catalyst used in photo-Fenton system and the applications in degradation removal of organic dye from wastewaters.
研究领域:
环境科学
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材料科学
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产品关联
DOI
PubMed
高影响因子
Water
·
2024
·Vol. 16
·期 21
·3109
·
IF 3
Zheng Zhang,Libin Zhao,Jingyuan Tian,Shaojie Ren,Wei Zhang
Persulfate-based advanced oxidation processes have emerged as a promising approach for the degradation of organic pollutants in aqueous environments due to their ability to generate sulfate radicals (SO4−·) within catalytic systems. In this study, peroxydisulfate (PDS) and peroxymonosulfate (PMS) were investigated with the natural vanadium–titanium magnetite (VTM) as the activator for the degradation of acid orange II. The degradation efficiency increased with higher dosages of VTM or persulfate (both PDS and PMS) at lower concentrations (below 10 mM). However, excessive PMS (higher than 10 mM) in the PMS/VTM system led to the self-consumption of free radicals, significantly inhibiting the degradation of acid orange II. The VTM-activated PDS or PMS maintained an effective degradation of acid orange II in a wide pH range (3~11), suggesting remarkable pH stability. The SO4−·was the main active species in the PDS/VTM system, while hydroxyl radical (·OH) also contributed significantly to the PMS/VTM system. In addition, PMS exhibited better thermal stability during VTM activation. Coexisting ions in an aqueous environment such as bicarbonate (HCO3–), carbonate (CO32–), and hydrogen phosphate (HPO42–) had obvious effects on persulfate activation. Our study systematically investigated the different activation processes and influencing factors associated with PDS and PMS when the natural VTM was used as a catalyst, thereby providing new insights into the persulfate-mediated degradation of organic pollutants in aqueous environments.
研究领域:
环境科学
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
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2016
·Vol. 92
·期 7
·1601-1612
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IF 2.738
Jiahua Lu,Qing Liu,Zhongduo Xiong,Zhijun Xu,Yingjie Cai,Qiang Wang
BACKGROUND Synthetic dyes are present in the wastewater from many industrial processes and they cause serious problems to human and aquatic life. The development of a novel and effective peroxymonosulfate (PMS) activator is proposed to eliminate dyes pollution. A new magnetic nanocomposite, Fe 3 O 4 @C/MnCo 2 O 4 , was prepared and characterized. The activity of Fe 3 O 4 @C/MnCo 2 O 4 as heterogeneous catalyst for PMS activation was evaluated by the decolorization of Acid Orange II (AO II). RESULTS With a ‘Fe 3 O 4 @C/MnCo 2 O 4 + PMS’ system, the dye solution could be nearly completely decolorized in about 25 min over a wide pH range (pH 4.1−8.1), and 98% removal could be achieved in 15 min without pH adjustment (pH = 6.38). The influence of solution pH, dosage of catalyst and PMS, reaction temperature, and PMS activation mechanism were studied. It was found that sulfate radicals were the primary species responsible for the oxidation of AO II. The catalyst was magnetically separable and displayed good stability and reusability, giving six cycles of use without deterioration in its performance. CONCLUSION This study demonstrated the simple recycling and high activity of Fe 3 O 4 @C/MnCo 2 O 4 composite in PMS activation for the decolorization of AO II solution. It provides a promising way for the decontamination of organic pollutants. © 2016 Society of Chemical Industry
研究领域:
环境科学
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化学工程
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DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2018
·
IF 5.091
Zhibo Yang,Liang Zhu,Lin Chen
Core-shell structured NH 2 -functionalized UiO-66 magnetic composites (γ-Fe 2 O 3 @C@UiO-66-NH 2 ) were fabricated via a simple, facile and green approach to investigate their adsorption behaviors towards different organic dyes (methylene blue, malachite green , acid fuchsin and acid orange II). Different characterization methods containing XRD , TEM , EDXA , FTIR, BET and XPS were used to indicate that the as-prepared γ-Fe 2 O 3 @C@UiO-66-NH 2 material exhibited core-shell structure and excellent surface performance. Adsorption experiments showed that γ-Fe 2 O 3 @C@UiO-66-NH 2 could selectively adsorb anionic dyes and effectively separate the mixture, which might be mainly ascribed to the negatively-charged anionic dyes as opposite to the positively-charged Zr metal sites in γ-Fe 2 O 3 @C@UiO-66-NH 2 . The kinetics and adsorption isotherm of acid orange II and acid fuchsin adsorption in γ-Fe 2 O 3 @C@UiO-66-NH 2 were also investigated. For acid orange II and acid fuchsin, the maximum adsorption capacity obtained from the Langmuir isotherm model was 48.12 mg/g and 31.54 mg/g, respectively. Moreover, γ-Fe 2 O 3 @C@UiO-66-NH 2 exhibited good structural stability and reusability, which suggesting that γ-Fe 2 O 3 @C@ UiO-66-NH 2 as an easy-prepared adsorbent material exhibited great application potential in the selective removal of dyes from water systems.
研究领域:
环境科学
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材料科学
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DOI
高影响因子
JOURNAL OF FOOD COMPOSITION AND ANALYSIS
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2024
·
IF 4
Zhaopeng Wang,Hui Lv,Yu Zhang,Yanan Li
Acid orange II (AO2) is a synthetic azo dye commonly used illegally in food production and processing. The development of a fast and effective analytical method is crucial for controlling the unlawful use of AO2 in food, especially in seasoning. Here, an antibody specific for AO2 was generated, with 1.01 ng/mL IC 50 and minimal cross-reactivity with other analogs (<1 %, including sunset yellow , tartrazine , para red, chromotrope FB, Sudan Ⅰ, rhodamine B , 2-naphthol, amaranth , ponceau 4 R and allura red AC). Furthermore, a highly sensitive quantum dot beads-based fluorescence immunochromatography assay (QBs-FICA) was established for AO2 determination. The assay had a working range of 23–287 μg/kg with a 11 μg/kg limit of detection (LOD) in chili powder and hotpot seasoning samples. Using spiked samples, the results of QBs-FICA were found to be consistent with those of liquid chromatography-tandem mass spectrometry. This indicates that QBs-FICA is a reliable, rapid, and portable tool for testing of AO2.
研究领域:
食品安全检测
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分析化学
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生物技术
✓ 已验证
产品关联
DOI
高影响因子
MATERIALS CHEMISTRY AND PHYSICS
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2022
·
IF 4.778
Huixin Xiong,Bailin Zhang,Can Cui,Yiqun Xu
The synthesized polyaniline/FeOOH composite characterized by SEM, HRTEM, XRD , FT-IR and BET, was used as adsorbent for Acid Orange II (AOII). The kinetics, isotherm and thermodynamics of AOII adsorption by polyaniline/FeOOH were studied by batch experiments. And effects of pH and coexisting ions on AOII removals were also investigated. Adsorption kinetics and isotherm well fitted pseudo second-order kinetic model and Langmuir isotherm model, respectively. The maximum adsorption capacity of polyaniline/FeOOH for AOII could reach 155.8 mg g −1 . It showed that polyaniline/FeOOH composite could rapidly and efficiently remove AOII from aqueous solutions. In addition, thermodynamic result indicated that the adsorption was a spontaneous endothermic process. Removal ratio of AOII (100 mg/L) increased as pH decreased and could reach 98.6% at pH3. And anions coexisting in the solutions could inhibit the adsorption effect, while the cations have negligible influence. Also, PANI/FeOOH had better applicability to the different types of anionic dyes. The regeneration of polyaniline/FeOOH loading 98.6% of AOII evaluated for three cycles and there was about 70% of AOII loaded on final adsorbent.
研究领域:
环境科学
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材料科学
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物理化学
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水处理技术
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吸附科学
✓ 已验证
DOI
高影响因子
ADVANCED POWDER TECHNOLOGY
·
2017
·
IF 2.659
Junhui Yi,Jiaxing Song,Huimei Mo,Yupeng Yang
Ag/AgVO 3 nanorods have been obtained for the first time by one step hydrothermal method with the contribution of pyridine. The prepared sample was systematically characterized. Their photocatalytic properties were investigated by degrading acid orange II (AO-II) under visible light. Compared with pure AgVO 3 , Ag/AgVO 3 nanorods showed much higher photocatalytic activity and stability. The enhanced photocatalytic activity was attributed to Ag nanoparticles (NPs) with a strong surface plasmon resonance (SPR). Further studies indicate that the photogenerated holes (h + ) and superoxide radical anions ( O 2 − ) were major active species. Ag/AgVO 3 nanorods has a huge potential application in wastewater treatment.
研究领域:
材料化学
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环境科学
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纳米科技
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光催化
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废水处理
✓ 已验证
DOI
高影响因子
DYES AND PIGMENTS
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2023
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IF 4.5
Qin Hu,Wenqian Sun,Lixia Xiao,Jie Han,Tianzu Guan,Wenyuan Zhou,Xiaojuan Gong,Zhen-quan Yang
This work for the first time presents a visual fluorescence paper sensor for accurate and on-site detection of acid orange II (AO 2 ) in food matrix, where green-emissive carbon nanodots (G-CDs) were exploited. The as-synthesized G-CDs had an average particle size of 3.9 ± 0.7 nm and displayed green emission at 511 nm upon excitation at 450 nm. When there existed AO 2 , the G-CDs fluorescence was effectively suppressed via inner filter effect (IFE) and dynamic interaction. The as-prepared G-CDs probe achieved a 0.01–25.0 μM linear scope and a 36.5 nM limit of detection. Particularly, owing to a distinguishable reduction in G-CDs emission intensity by a smartphone application , a visual probing platform along with a nanopaper-based device were be developed for recognizing AO 2 . The corresponding detection limits were severally 0.61 μM and 1.39 μM. Success was achieved in applying our fluorescence approaches for detecting AO 2 in Yuba, chili powder, sunflower seeds, tomato paste and orange juice samples, attaining desirable results. The present work underlines the potential of smartphone-integrated nanopaper based on CDs as an encouraging candidate for on-site AO 2 recognition in food matrix.
研究领域:
分析化学
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食品科学
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纳米技术
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）