Crystals
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2018
·Vol. 8
·期 6
·250
·
IF 2.144
Xue-Qing Zhan,Xiao-Yan Yu,Fang-Chang Tsai,Ning Ma,Huan-Li Liu,Yu Han,Lei Xie,Tao Jiang,Dean Shi,Yan Xiong
Owing to their high surface area and porosity, metal-organic frameworks (MOFs) have been gradually employed for a myriad of applications ranging from sensing, pollutant adsorption, and drug delivery to environmental remediation and catalysis. Magnetic nanoparticles-metal-organic frameworks (MMOFs) hybrid materials can facilitate facile removal of MOFs from solutions. In this report, we report the synthesis of Fe3O4@UiO-66 by encapsulation and simulated the drug loading and release by studying the adsorption and release of AO7. Thus, we loaded these MMOFs with AO7 and found that they were able to trigger and control its release by simply applying an external magnetic field. The magnetic field heats the magnets in the MOF, which causes the load to burst from the framework.Keywords:magnetic MOFs;triggered release;targeted delivery;AO7
研究领域:
环境科学
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材料科学
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药物递送
✓ 已验证
产品关联
DOI
高影响因子
Journal of Cleaner Production
·
2019
·
IF 6.395
Yi Wan,Ze-Yu Liu,Peng Song,Xiao-Qi Zhang,Jiang-Chao Song,Yu-Jie Fu,Xiao-Hui Yao,Jun Wang,Tao Chen,Dong-Yang Zhang,Long Li,Can-Yang Shi
In this study, a three-dimensional porous cellulose-based microsphere material modified with ionic liquid functional groups was prepared. Seven kinds of cellulose microspheres with different ionic liquid groups were successfully produced and were used for the adsorption of Acid Orange 7 dye. Cellulose microsphere modified with 4-methylimidazole, named as CMs4, had the greatest adsorption capacity of 218.6 mg/g and the fastest adsorption rate. CMs4 reached an adsorption capacity of 100 mg/g after only 10 min. Compared with materials in other literatures, CMs4 had an excellent Acid Orange 7 dye adsorption rate. According to the zeta potential analysis, the surface potential of CMs4 depended on the pH. Exploiting this property, cationic and anionic dyes can be separated using CMs4 by changing the pH. Since cellulose materials are renewable and widely available, CMs4 is a promising environmentally friendly material for dye adsorption applications.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2022
·
IF 9.136
Yuhan Long,Songrong Li,Peizhen Yang,Xi Chen,Wenhao Liu,Xuesong Zhan,Cheng Xue,Dongfang Liu,Wenli Huang
MOF-derived metal-carbon composite catalyst was an alternative high-efficient catalyst for activating peroxymonosulfate (PMS). In this study, a novel cobalt-carbon-nitrogen doped composite catalyst with honeycomb porous structure (Co-HPNC) was obtained through a simple strategy consisting of three steps: self-growth of ZIF-67 on the SiO 2 core, pyrolysis, and NaOH etching away SiO 2 core. The Co-HPNC exhibited an outstanding catalytic performance (98.1% in 10 min) to activate PMS for acid orange 7 (AO7) degradation. The observed reaction kinetic constant (0.4319 min −1 ) was 2.64 times superior to that of the unmodified Co/NC catalysis system (0.1636 min −1 ). In the meantime, the catalyst demonstrated a high PMS activation capacity over a wide pH range of 3–11 and strong adaptability to the high concentration of inorganic anions (Cl - , SO 4 2- , and CO 3 2– ). After being recycled three times, the removal efficiency could still reach 92.7% in 25 min. The quenching tests and EPR spectrum illustrated the existence of radical and non-radical pathways, in which singlet oxygen was dominant during the degradation process. It was hypothesized that Co(0)/Co(Ⅱ)/Co(Ⅲ), pyridinic-N and pyrrolic-N contributed to the generation of hydroxyl and sulfate radicals, while C=O functional group and graphitic-N were catalytic sites for singlet oxygen. Finally, the radical electrophilic attacking sites of AO7 were calculated by the density functional theory (DFT), and the degradation routes of AO7 were speculated by GC–MS. The toxicity test illustrated that the Co-HPNC/PMS system was an environmental-friendly technology for AO7 degradation. The prepared Co-HPNC with a unique honeycomb porous structure presents a novel synthesis route for MOF-derived catalyst applied in the PMS activation system for wastewater treatment.
研究领域:
环境科学
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催化
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材料科学
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水处理
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
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2021
·
IF 10.588
Siqi Tong,Dan Chen,Ping Mao,Xinbai Jiang,Aiwu Sun,Zhixiang Xu,Xiaodong Liu,Jinyou Shen
A novel magnetic hydrochar synthesized from Fenton sludge (FS) and sewage sludge (SS) was employed in the anaerobic decolorization of acid orange 7 (AO7). The stable presence of Fe 3 O 4 in magnetic hydrochar was confirmed by physicochemical characterization. The degradation efficiency of AO7 in the anaerobic system with the addition of hydrochar prepared in an optimal proportion (SS:FS=1:3, named as HC-1:3) could reach 98.55%, which was 1.91 times higher than the control system. Particularly, superior electrical conductivity, electron transport system activity and azo reductase activity of the sludge in anaerobic system with HC-1:3 were achieved. The redox of Fe(Ⅲ)/Fe(Ⅱ) in anaerobic system was realized by dissimilatory iron-reducing bacteria enriched with HC-1:3. According to the six-cycle batch experiments and 120-day continuous-flow UASB experiments, the addition of HC-1:3 into the anaerobic system facilitated the diversity of microbiological community and increased the ecological stability of anaerobic system. The possible electron transfer mechanism involving in the magnetic hydrochar-based anaerobic system for AO7 removal was speculated preliminarily. The as-prepared magnetic hydrochar not only showed a promising future in anaerobic system for recalcitrant contaminants degradation, but also provided a new approach for the resource utilization of FS and SS.
研究领域:
环境科学
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废水处理
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材料科学
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生物技术
✓ 已验证
DOI
PubMed
高影响因子
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
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2016
·Vol. 92
·期 4
·827-833
·
IF 2.738
Jinxi Feng,Shenyu Lan,Chunyang Yao,Ya Xiong,Shuanghong Tian
BACKGROUND Electro-generation of NaOH and H 2 SO 4 with organic compound-free Na 2 SO 4 wastewater has been known for many years, but actually, lots of Na 2 SO 4 wastewater contains organic pollutants, such as black liquor, dyeing and sulphonating wastewater etc., therefore, there is a strong demand for investigations on performance and effect of the organic pollutants in electrochemically splitting Na 2 SO 4 into H 2 SO 4 and NaOH from these wastewaters. RESULTS Co-electrolysis of Na 2 SO4 (1.13 mol L −1 ) and AO7 (50 ∼ 500 mg L −1 ) was investigated in a diaphragm cell with IrO 2 -coated Ti electrodes. It was found that the concentrations of the resulting NaOH and H 2 SO 4 could remain at about 0.73 mol L −1 and 0.36 mol L −1 , respectively, although the COD removal was increased from 50.3 mg L −1 to 166.3 mg L −1 with the increase of AO7 concentration, for 120 min. CONCLUSION In a diaphragm cell with IrO 2 -coated Ti electrodes, NaOH and H 2 SO 4 could be effectively generated, and simultaneously, AO7 could also be degraded for the wastewater containing Na 2 SO 4 and AO7. Interestingly, the electro-generation of NaOH and H 2 SO 4 was not significantly affected by the occurrence and degradation of AO7 in the range 0–500 mg L −1 . The phenomenon of constant acid–base yield contributed to the independence of the main acid-generating reactions on the electro-oxidation of AO7. © 2016 Society of Chemical Industry
研究领域:
环境科学
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电化学工程
✓ 已验证
DOI
高影响因子
Journal of Cleaner Production
·
2024
·
IF 9.7
Weixin Xian,Wenyu Wang,Juntao Guo,Jinjun Li,Jing Xu,Feng Wu
FePO 4 (FP) as a precursor of lithium iron phosphate batteries has been mass-produced in recent years and may face the problem of overproduction. Also, the phosphorus removal process in wastewater treatment plants produces large amounts of sludge containing FP. It is a huge waste of both iron and phosphorus resources if such FP cannot be utilized. This work explores a new strategy for utilizing FP to activate sulfite (S(IV)) autoxidation for simultaneous pollutant degradation and phosphorus release in water. Acid orange 7 (AO7) and several pharmaceutical and personal care products (PPCPs) were chosen as the target pollutants for the FP‒S(IV) system and the influence of pH, FP and S(IV) dosage were investigated. Typically, up to 89.5% AO7 (10 mg L −1 ) and above 60% PPCPs (10 μM) were oxidized within 90 min by adding 1 g L −1 FP and 2 mM S(IV) into the water at the initial pH 4.0. Results of quenching experiments and electron spin resonance analysis confirmed SO 5 •− as the dominant reactive species for AO7 oxidation. Meanwhile, two stages of phosphorus release from FP were observed along with the AO7 oxidation and their linear correlation over the pH range 3.0–8.0 was proven. The first stage (0–5 min) was thought to be dependent on the initial pH and was obviously faster than the second stage (10–45 min), whose rate increased linearly with S(IV) dosage. Phosphorus released high up to 24.3 μM at 90 min with 4 mM S(IV). Moreover, the mechanisms of FP activated sulfite autoxidation as well as phosphorus release were proposed, and the AO7 degradation pathway was investigated. This study provides a novel possibility for FP waste utilization and potential recovery of phosphorus resources.
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 WATER SUPPLY RESEARCH AND TECHNOLOGY-AQUA
·
2018
·Vol. 67
·期 5
·472-483
·
IF 1.179
Liu ChaoRong,Zhang Jing,Wang Qingguo,Zhang Wei,Zhou Peng,Hu Sikui,Zhang Gucheng
A heterogeneous system using nanoscale zero-valent copper (nZVC) as an activating agent via ultrasound (US) accleration was employed for the degradation of azo dye acid orange 7 (AO7). The degradation rate of AO7 was obviously promoted by ultrasound irradiation as compared to the silent system from 28.83% to 87.39% at 5 min. Via the surface characteristics detected by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and scanning electron microscopy (SEM), it was indicated ultrasound can accelerate the corrosion process of nZVC as more Cu + was generated at the same reaction time. Via the particle size detected it was proved US has the ability to disperse the aggregates of nZVC. The addition of neocuproine hemihydrates (NCP) proved Cu + is the primary activating agent and a large number of free radicals (OH• and SO 4 − •) were detected by adding methyl alcohol (MA) and tert butyl alcohol (TBA). Then, the parameters investigated were the ultrasound power, acid concentration, and nZVC dosage. The results showed that the increase of ultrasound power has few impacts on AO7 degradation, and with the increase of acid concentration and nZVC dosage, the degradation rate of AO7 was enhanced remarkably. As seen from the above results, it is clear that ultrasound enhances the release of Cu + to participate in the process of AO7 removal.
✓ 已验证
DOI
高影响因子
CHEMOSPHERE
·
2019
·
IF 5.108
Zhihua Sun,Shiyao Li,Haojie Ding,Yunhua Zhu,Xuxu Wang,Huanfang Liu,Qin Zhang,Chun Zhao
Acid Orange 7 (AO7), as a most common and widely used synthetic dyes in the printing and dyeing industry, was hardly degradable by traditional wastewater treatment methods. Here, activated carbon fiber (ACF) as an in-situ regenerated cathodic adsorbent in the electrochemical/Fe 3+ /peroxymonosulfate process (EC/ACF/Fe 3+ /PMS) was firstly investigated for AO7 removal and compared with several different processes. The results indicated that the effective adsorption of AO7 on ACF can be enhanced under electrolytic conditions, while the adsorbed AO7 on ACF can be completely degraded and mineralized in EC/ACF/Fe 3+ /PMS process resulting in the in-situ regeneration of ACF. Besides, the electrical energy per order values were investigated, which showed an apparent reduction of electrical energy consumption from 0.42831 to 0.09779 kWh m −3 when ACF-cathode replaced Pt-cathode. Further study revealed that higher conversion rate of Fe 2+ from Fe 3+ was observed with ACF-cathode. It deserved to be mentioned that the removal efficiency of AO7 was satisfactory and stable even after reusing ACF cathode for 10 times. Furthermore, structure and elements of ACF surface were investigated, which indicated the structure of ACF was intact in EC/ACF/Fe 3+ /PMS due to inhibition of ACF corrosion by electron migration at cathode. In addition, the total iron content of the effluent in EC/ACF/Fe 3+ /PMS was lower than that of EC/Fe 3+ /PMS due to the deposition of iron on ACF-cathode surface. Therefore, advantages of EC/ACF/Fe 3+ /PMS for AO7 degradation were not only a much higher oxidation efficiency and in-situ regenerated cathodic adsorbent, but also a lower electrical energy consumption and lesser iron ions contents in the effluent.
研究领域:
环境科学
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化学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
WATER AIR AND SOIL POLLUTION
·
2016
·Vol. 227
·期 10
·1-8
·
IF 1.551
Li Ying,Yang Lijiao,Chen Cheng,Lan Yeqing
In this paper, Zn(0)-catalyzed ozonation degradation of acid orange 7 (AO7) and its impact factors including solution pH, Zn loading, and AO7 initial concentration were investigated through a series of bath experiments. The results demonstrated that Zn could markedly accelerate the degradation of AO7 by ozone (O 3 ) and the degradation efficiency of AO7 increased by 77 and 71 % within 30 min as compared with those in the systems of O 3 alone and Zn/air, respectively. The reuse of Zn resulted in a slight decline in AO7 degradation, suggesting that a coating of ZnO on the surface of Zn particles weakened Zn catalytic activity. The optimal removal of AO7 was achieved in a wide pH range of 4 to 10, and a lower or higher pH was not conducive to the degradation of AO7. In addition, the degradation efficiency of AO7 increased with Zn loading but decreased with AO7 initial concentration. The introduction of free radical scavengers into the system of AO7/Zn/O 3 confirmed that O 2
•− , rather than •OH, was the main free radicals responsible for the rapid removal of AO7. The degradation of AO7 by O 3 assisted with Zn could be well expressed with pseudo-first-order kinetic model.
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
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2022
·Vol. 29
·期 31
·47549-47560
·
IF 5.19
You Wenqiao,Li Youlin,He Dandan,Zeng Youmei,Zhu Jiangwei,You Xiaofeng,Wang Kang,Zhou Guangming,Peng Guilong
In the present study, pyrophosphate (PP) was used to activate peroxymonosulfate (PMS) for acid orange 7 (AO7) removal under neutral pH conditions. The removal rate of AO7 (20 mg/L) was 84% within the reaction time with a rate constant value of 0.0165 min −1 under optimum conditions. Additionally, the effects of the concentrations of PMS and PP in solutions with various pH values and the coexisting inorganic anions on AO7 removal were measured. In addition, the performance of phosphate (P(V)) on PMS activation was compared with that of phosphite (P(III)) species. In contrast to P(III), the concentration of P(V) showed a positive correlation with the efficiency of AO7 decolorization. PMS activation in different types of buffer solutions was also examined, and the results indicated that the decolorization efficiency of AO7 induced by PP addition, and the buffer solution also contributed to PMS self-decomposition. Singlet oxygen ( 1 O 2 ) might be the primary reactive oxygen species (ROS) in the PP/PMS system in which AO7 is decolorized at an initial pH of 7.06, as indicated by quenching experiments and electron spin resonance (ESR) tests. Therefore, PP/PMS systems may be promising technologies for removing organic contaminants, particularly for PP-rich electroplating wastewater.
研究领域:
环境科学
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化学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMOSPHERE
·
2017
·
IF 4.208
Yang Li,Lei Li,Zi-Xi Chen,Jie Zhang,Li Gong,Yi-Xuan Wang,Han-Qing Zhao,Yang Mu
Advanced oxidation processes offer effective solutions in treating wastewater from various industries. This study is the first time to investigate the potential of carbonate-activated hydrogen peroxide (CAP) oxidation process for the removal of organic pollutant from highly alkaline wastewaters. Azo dye acid orange 7 (AO7) was selected as a model pollutant. The influences of various parameters on AO7 decolorization by the CAP oxidation were evaluated. Furthermore, the active species involved in AO7 degradation were explored using scavenger experiments and electron spin resonance analysis. Additionally, AO7 degradation products by the CAP oxidation were identified to elucidate possible transformation pathways. Results showed that the CAP oxidation had better AO7 decolorization performance compared to bicarbonate-activated hydrogen peroxide method. The AO7 decolorization efficiency augmented from 3.70 ± 0.76% to 54.27 ± 2.65% when carbonate concentration was increased from 0 to 50 mM at pH 13.0, and then changed slightly with further increasing carbonate concentration to 70 mM. It increased almost linearly from 5.95 ± 0.32% to 94.03 ± 0.39% as H 2 O 2 concentration was increased from 5 to 50 mM. Moreover, trace amount of Co(II) could facilitate AO7 decolorization by the CAP reaction. Superoxide and carbonate radicals might be the main reactive oxygen species involved in the CAP process. Finally, a possible degradation pathway of AO7 by the CAP oxidation was proposed based on the identified products.
研究领域:
环境科学
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化学工程
✓ 已验证
DOI
PubMed
高影响因子
WATER SCIENCE AND TECHNOLOGY
·
2022
·Vol. 85
·期 7
·2038-2050
·
IF 2.43
Zhang Ming,Zhang Kuo,Zhou Runjuan,Wang Jinpeng
In this study, a new type of iron/copper bimetallic combined with hydroxylamine (HA) activated peroxymonosulfate (PMS) was constructed to treat organic pollutants. Selecting the azo dye acid orange 7 (AO7) as the representative of organic pollutants, the new system can achieve nearly 100% degradation of AO7 within 5 min. The Fe(III)/Cu(II)/HA/PMS system mainly generates SO 4 ·− to achieve the degradation of AO7 in acidic environment, while neutral and alkaline environments rely on · OH. The presence of hydroxylamine accelerates the cycle of Fe(III)/Fe(II) and Cu(II)/Cu(I) in the system, and enhances the degradation ability of the system for organic pollutants. The addition of trace Cu(II) (1 μM) enhances the ability of a single Fe(III)/HA/PMS system to degrade AO7 in neutral and alkaline environments without causing secondary copper pollution. The common inorganic anions Cl − and NO 3 − in water have almost no effect on the degradation of AO7 in the system. The constructed Fe(III)/Cu(II)/HA/PMS system is an efficient and clean organic pollutant wastewater treatment process, which has very promising application prospects. The effect of hydroxylamine on the activation of peroxymonosulfate in Fe(III)-Cu(II) bimetallic is reported for the first time. The Fe(III)/Cu(II)/hydroxylamine/peroxymonosulfate system can remove 100% of AO7 within 5 min. Hydroxylamine enables Fe(III), which cannot activate peroxymonosulfate, to activate peroxymonosulfate efficiently. A trace amount of Cu(II) can reduce Fe(III) to Fe(II).
研究领域:
环境化学
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高级氧化技术
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水处理技术
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）