CHEMICAL ENGINEERING JOURNAL
·
2014
·
IF 4.058
Ming-Xia Wang,Qi-Lei Zhang,Shan-Jing Yao
Mycelial pellets prepared using a marine-derived Penicillium janthinellum sp. strain (P1) were applied as biosorbents to remove dyes from aqueous solutions. Nine different dyes were studied and the effects of pH and salt concentration on the decolorization processes were investigated. The results showed that the mycelial pellet was effective in removing dyes from their water solutions. Moreover, it was found that pH was an important factor of the decolorization process and the best dye removal performance was achieved when pH = 5.0. The adsorption process of the live mycelial pellets was not affected by high salt concentrations. In addition, the mycelial pellets retained 91.3% of the original decolorization activity after five reusing cycles without any desorption treatments. The adsorption isotherms indicated that the biosorption process agreed well with the Langmuir isotherm model with a maximum biosorption capacity of 344.83 mg g(dry) − 1 and the kinetic adsorption results showed that the biosorption process followed a pseudo-second-order kinetic model.
研究领域:
环境微生物学
·
环境工程
·
生物吸附
·
水污染控制
·
应用微生物学
·
环境化学
✓ 已验证
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2017
·
IF 6.065
Li Fang,Liang Li,Zan Qu,Haomiao Xu,Jianfang Xu,Naiqiang Yan
A novel method was developed and applied for the treatment of simulated wastewater containing multiple heavy metals. A sorbent of ZnS nanocrystals (NCs) was synthesized and showed extraordinary performance for the removal of Hg 2+ , Cu 2+ , Pb 2+ and Cd 2+ . The removal efficiencies of Hg 2+ , Cu 2+ , Pb 2+ and Cd 2+ were 99.9%, 99.9%, 90.8% and 66.3%, respectively. Meanwhile, it was determined that solubility product ( K sp ) of heavy metal sulfides was closely related to adsorption selectivity of various heavy metals on the sorbent. The removal efficiency of Hg 2+ was higher than that of Cd 2+ , while the K sp of HgS was lower than that of CdS. It indicated that preferential adsorption of heavy metals occurred when the K sp of the heavy metal sulfide was lower. In addition, the differences in the K sp of heavy metal sulfides allowed for the exchange of heavy metals, indicating the potential application for the sequential removal and separation of heavy metals from wastewater. According to the cumulative adsorption experimental results, multiple heavy metals were sequentially adsorbed and separated from the simulated wastewater in the order of the K sp of their sulfides. This method holds the promise of sequentially removing and separating multiple heavy metals from wastewater.
研究领域:
环境科学
·
环境工程
·
纳米材料
·
水污染控制
·
化学工程
✓ 已验证
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2019
·
IF 7.65
Xingyun Hu,Xianjia Peng,Linghao Kong,Feng Zhu
The most toxic and mobile form of vanadium (V) is V(V). Thus, the oxidation of V is a subject of considerable importance since the process may increase environmental risks of V. V(IV) is known to be stable when pH < 4.5. However, in this study, stable V(IV) was oxidized almost completely in goethite suspension within 60 min at pH 2.0 and pH 4.0, correspondingly, only 25%–30% and 15%–20% of V(IV) were oxidized in equimolar Fe 3+ solution and the blank solution, respectively. The promoted oxidation of V(IV) by FeOOH is attributed to the formation of the complex, VO(OFe<) + or VO(OFe<) 2 . On the one hand, the formation of the complex caused higher pH in the interface of solid FeOOH and corresponding lower conditional potential of V(V)/V(IV) than those in bulk solutions, which facilitates the oxidation of V(IV). On the other hand, the surface group OFe < may serve as a medium that facilitating the electron transfer from V(IV) ions to dissolved oxygen molecules, also favoring the oxidation of V(IV). This study not only deepens our understanding of the transfer, transformation, and risk of V in environments, but also provides a reference to speculate the fate of similar elements in environments.
研究领域:
环境化学
·
地球化学
·
水污染控制
·
金属形态转化
·
界面过程
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DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2015
·
IF 7.435
Peng Yi-Zhu,Ma Wan-Hong,Jia Man-Ke,Zhao Xiao-Rong,David M. Johnson,Huang Ying-Ping
In this study, a weakly polar pesticide acetochlor in water was tried to degrade by BiOBr catalysts under visible light irradiation. Its degradation reaction rate increased exponentially with increasing catalyst dosage, which was significantly different from conventional photocatalytic patterns established for polar or water-soluble pollutants. Thus, the rate-dosage relationship of BiOBr/acetochlor was compared to that of BiOBr/Rhodamine B (RhB) (a typical strong polar dye pollutant in water) at different BiOBr dosages. The degradation rate of RhB increased with the BiOBr dosage and then plateaued due to more catalyst particles blocking the light into the inner solution, which is a typical behavior for heterogeneous photocatalysis of polar organic compounds in aqueous solution. While acetochlor behaved differently, its degradation rate increased exponentially with the BiOBr dosage, and no plateau was observed even up to 9.0 g/L BiOBr dosage. This special rate-dose relationship for weakly polar acetochlor was correlated with a unique adsorption property of BiOBr to acetochlor in water solution. There was a re-distribution effect that always exclude excessive acetochlor adsorbed on BiOBr surface regardless either substrates or BiOBr overdose. This finally resulted in every BiOBr particle having enough adsorption sites available for dissolved dioxygen to function thereby accelerate the degradation of weakly polar organic compounds in water.
研究领域:
环境化学
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光催化
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水污染控制
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环境功能材料
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污染物降解机制
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DOI
高影响因子
BIORESOURCE TECHNOLOGY
·
2022
·
IF 11.889
Shengnan Li,Mingsi Gao,Heng Dong,Yuxin Jiang,Wanting Liang,Jiwei Jiang,Shih-Hsin Ho,Fengxiang Li
The misuse of antibiotics has increased the prevalence of antibiotic resistance genes (ARGs), considered a class of critical environmental contaminants due to their ubiquitous and persistent nature. Previous studies reported the potentiality of bio-electro-Fenton processes for antibiotic removal and ARGs control. However, the production and fate of ARGs in bio-electro-Fenton processes triggered by microbial fuel cells are rare. In this study, the norfloxacin (NFLX) average residual concentrations within two days were 2.02, 6.07 and 14.84 mg/L, and the average removal efficiency of NFLX was 79.8 %, 69.6 % and 62.9 % at the initial antibiotic concentrations of 10, 20 and 40 mg/L, respectively. The most prevalent resistance gene type in all processes was the fluoroquinolone antibiotic gene. Furthermore, Proteobacteria was the dominant ARG-carrying bacteria. Overall, this study can provide theoretical support for the efficient treatment of high antibiotics-contained wastewater by bio-electro-Fenton systems to better control ARGs from the perspective of ecological security.
研究领域:
环境微生物学
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水污染控制
·
分子生态学
·
环境工程
·
抗生素耐药性
·
电化学高级氧化
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DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2021
·
IF 10.588
Fangyuan Zhang,Mei Hong,Jing Bai,Zhi Liu,Aiyuan Jia,Zhisheng Liu,Can Shi,Yangxue Li
Levofloxacin (LEV) infiltrated in groundwater has threatened the safety of drinking water . For in-situ remediation of LEV-contaminated groundwater, there exists a main challenge of exploiting proper high efficient backfill medium in utilizing charming permeable reactive barriers (PRBs). Herein, three porous shapeable three-component hydrogen-bonded covalent organic aerogels (H C OA-1, H C OA-2 and H C OA-3) were fabricated based on a multiple-linking-site strategy to evaluate for adsorptive removal of LEV. The three H C OAs exhibited satisfactory performance in LEV adsorption that could integrate high adsorption capacity, good antiion interference, excellent recyclability and wide pH tolerance. The different regularity of kinetics and isotherms of three H C OAs signified that electrostatic effect, pore preservation, hydrogen bonding probably govern the adsorption process in combination, coupling with π-π electron-donor-acceptor (EDA), dipole-dipole and hydrophobic-hydrophobic interaction besides. In addition, the response surface methodology (RSM) was employed for studying the single and synergetic effects of selected variables and optimizing operation conditions. Furthermore, a laboratory PRB column packed with processable H C OA-2 was set up to investigate the LEV removal, and the breakthrough data was explained by Adams-Bohart, Thomas, BDST and Yoon-Nelson models. We believe could hopefully bring H C OAs into the real in-situ remediation of such challenging and persistent LEV-polluted groundwater with further massive-scale efficiently.
研究领域:
环境科学
·
材料科学
·
水污染控制
·
环境功能材料
·
污染物吸附
·
可持续修复技术
✓ 已验证
DOI
高影响因子
DYES AND PIGMENTS
·
2021
·
IF 4.889
Lu Li,Xugang Dong,Zhanfang Liu,Juan Wei,Jingru Li,Hong Zhou,Jun Zhu,Xinwei Shi
In this study, a visual and ultrasensitive method for the determination of trace mercury ions in water was developed based on the high efficiency of urease catalysis and pH-sensitive inverse opal polymeric photonic crystals (IOPPCs). Mercury ions can inhibit urea hydrolysis and suppress the production of ammonium and bicarbonate ions in the solution, resulting in the redshift of IOPPCs. Therefore, the redshift of IOPPCs Bragg diffraction is directly related to the concentration of mercury ions. Meanwhile, the color of IOPPCs varied significantly with the shift of the Bragg diffraction wavelength, thus achieving the visual semi-quantitative detection of mercury ions by the naked eye. The minimum detection concentration of this method is 5 × 10 −16 g/L, which is much lower than the maximum contaminant level for the safe drinking of water (2 × 10 −6 g/L) recommended by the environmental protection agency (EPA), USA. In addition, this is a simple and quick method for effective on-site detection of mercury ions, which shows a great promise in emergency leakage monitoring and control.
研究领域:
分析化学
·
环境监测
·
生物传感器
·
纳米材料
·
分子诊断
·
水污染控制
✓ 已验证
DOI
高影响因子
RSC Advances
·
2016
·Vol. 6
·期 79
·75855-75861
·
IF 3.289
Qixuan Song,Hui Wang,Baoshan Yang,Fei Wang,Xinrong Sun
A novel silver nanoparticle-modified magnetic multi-walled carbon nanotube composite (Ag-FMWCNTs) was synthesized by embedding Fe3O4 and assembling Ag nanoparticles in one-step. The properties of the Ag-FMWCNTs composites and magnetic multi-walled carbon nanotubes (FMWCNTs) were studied by scanning electron microscopy, vibrating sample magnetometry (VSM) and Fourier transform infrared spectroscopy. The adsorption isotherms, adsorption kinetics and the effects of solution pH and ionic strength to adsorb emerging contaminant sulfamethoxazole (SMX) from aqueous solution on different multi-walled carbon nanotubes-based adsorbents were determined. The results showed that the adsorption kinetics could be explained well by means of the pseudo-second-order and intraparticle diffusion models. The pH experiments showed that maximum adsorption occurred at pH 4. Additionally, all adsorbents had a strong adsorption ability to SMX and the Langmuir maximum capacity followed the order: 5% Ag-FMWCNTs (118.58 mg g−1) > 3% Ag-FMWCNTs (86.41 mg g−1) > MWCNTs (73.69 mg g−1) > 1% Ag-FMWCNTs (70.26 mg g−1) > FMWCNTs (45.13 mg g−1). The spent adsorbents were regenerated in methanol. It was also found that after regenerating four times, multi-walled carbon composites retained up to 80% of their original adsorption performance. Therefore, the Ag-FMWCNTs composite could be used as a potential adsorbent for removing sulfamethoxazole from water.
研究领域:
环境科学
·
纳米技术
·
水污染控制
·
吸附材料
·
药物残留治理
✓ 已验证
DOI
高影响因子
Desalination and Water Treatment
·
2024
·
IF 1
Hongyuan Qin,Jiawei Huang,Xueli Zhang,Ling Yu,Yang Yu
In this study, lanthanum hydroxide adsorbent was synthesized through a simple hydrothermal method and applied for removing phosphate from water. The optimal adsorbent was obtained at the La/OH molar ratio of 4:1. The adsorbent showed rapid adsorption of phosphate within the first 4 h in which approximately 84% of the equilibrium adsorption capacity can be achieved. The phosphate uptake was highly dependent on solution pH. The better fit of the Langmuir isotherm model to experimental data indicated that the monolayer adsorption occurred and the maximum adsorption capacity of 193.9 mg/g was accomplished at pH 7.0. The presence of fluoride could significantly retard the uptake of phosphate. X-ray photoelectron spectroscopy analysis indicated that hydroxyl groups on the adsorbent surface played the most key role in the adsorption. The phosphate ions were adsorbed on the adsorbent through the formation of inner-sphere complexes.
研究领域:
环境化学
·
纳米材料科学
·
水污染控制
·
表面化学
·
吸附科学
✓ 已验证
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2021
·
IF 10.588
Keng Xuan,Juan Wang,Zhiheng Gong,Xuegang Wang,Jun Li,Yadan Guo,Zhanxue Sun
In this work, nanoscale hydroxyapatite (HAP)-modified ZIF-67 composite, HAP/ZIF-67, with abundant functional groups for uranium(VI) binding was synthesized via a facile ultrasound-assisted synthesis method. The prepared HAP/ZIF-67 was characterized by XRD , SEM, TEM , BET, FT-IR and XPS techniques, and was applied to eliminate uranium(VI) from aqueous solutions under various conditions, i.e., pH, coexisting ions, temperature and contact time. The results indicate that the abundant Co-OH, -C N- and -NH- binding groups originating from the ZIF-67 and the Ca-OH and PO 4 3- derived from loaded nanoscale HAP synergistically endowed HAP/ZIF-67 with the excellent U(VI) adsorption capacity of 453.1 mg/g, which is 2.55 and 1.78 times that of pristine HAP and ZIF-67. HAP/ZIF-67 showed high adsorption selectivity toward U(VI), and the U(VI) elimination efficiency for real wastewater by HAP/ZIF-67 reached 97.29%. The adsorption kinetics and isotherms were well simulated by the pseudo-second-order model and Langmuir isotherm model, respectively, suggesting that U(VI) adsorption was an endothermic monolayer chemisorption process. The adsorption mechanism of U (VI) by HAP/ZIF-67 was dominated by surface complexation process. This work is expected to provide an effective strategy for developing HAP-modified MOFs absorbent to be used for the highly efficient elimination of radionuclides from wastewater.
研究领域:
环境科学
·
材料科学
·
核化学
·
水污染控制
·
吸附技术
·
功能材料
·
放射性核素去除
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2018
·
IF 2.829
Yueyun Fang,Qizhang Huang,Pengyi Liu,Jifu Shi,Gang Xu
This study demonstrated high-efficient dye adsorption for wastewater using MoS 2 -glue sponge as an easy-separative and regenerative adsorbent. Flower-like molybdenum disulfide (MoS 2 ) nanopowders with rich polar edge sites were firstly synthesized by a facile one-pot hydrothermal method . Chemical and morphological features of MoS 2 nanoflowers were then examined by XRD , XPS , SEM and TEM . Afterwards, different concentrations of the MoS 2 -glue sponges with easy separability were successfully fabricated by a convenient two-step dip-coating method. The adsorption performance was estimated by the removal of Rhodamine B (RhB) dyes. The results proved that the maximum adsorption capacity of MoS 2 -glue sponge was 127.39 mg RhB/g product in 60 min. The RhB uptake behaviors can be well described by the Sips isotherm model and pseudo-second-order kinetic model , indicating a multilayer and chemical adsorption process. The adsorption mechanism proposed that the zwitterionic RhB molecules in aqueous solution would aggregate on the surface of negative charged MoS 2 in a head-to-tail way through electrostatic interaction . Furthermore, RhB dyes could desorb easily from MoS 2 -glue sponges when changing the polarity of solvent and the reusability experiment showed that the MoS 2 -3% glue sponge could be reused for 15 times with above 85.8% of the adsorption capacity retained. Thus, the novel MoS 2 -glue sponge is considered as a competitive adsorbent for treatment of dyestuff waste water.
研究领域:
环境科学
·
材料科学
·
纳米技术
·
化学工程
·
水污染控制
✓ 已验证
DOI
高影响因子
ENVIRONMENTAL SCIENCE & TECHNOLOGY
·
2018
·
IF 6.653
Chen Tian,Jian Zhao,Xinwen Ou,Jieting Wan,Yuepeng Cai,Zhang Lin,Zhi Dang,Baoshan Xing
p-Arsanilic acid (p-ASA) is an emerging organoarsenic pollutant comprising both inorganic and organic moieties. For the efficient removal of p-ASA, adsorbents with high adsorption affinity are urgently needed. Herein, amine-modified UiO-67 (UiO-67-NH2) metal–organic frameworks (MOFs) were synthesized, and their adsorption affinities toward p-ASA were 2 times higher than that of the pristine UiO-67. Extended X-ray absorption fine structure (EXAFS), X-ray photoelectron spectroscopy (XPS), and density functional theory (DFT) calculation results revealed adsorption through a combination of As–O–Zr coordination, hydrogen bonding, and π–π stacking, among which As–O–Zr coordination was the dominant force. Amine groups played a significant role in enhancing the adsorption affinity through strengthening the As–O–Zr coordination and π–π stacking, as well as forming new adsorption sites via hydrogen bonding. UiO-67-NH2s could remove p-ASA at low concentrations (<5 mg L–1) in simulated natural and wastewaters to an arsenic level lower than that of the drinking water standard of World Health Organization (WHO) and the surface water standard of China, respectively. This work provided an emerging and promising method to increase the adsorption affinity of MOFs toward pollutants containing both organic and inorganic moieties, via modifying functional groups based on the pollutant structure to achieve synergistic adsorption effect.
研究领域:
环境科学
·
材料化学
·
吸附技术
·
水污染控制
·
理论化学
·
X射线光谱学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）