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Ciprofloxacin
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2020 ·Vol. 27 ·期 18 ·22806-22817 · IF 3.056

Ciprofloxacin adsorption by biochar derived from co-pyrolysis of sewage sludge and bamboo waste

Li Jie,Yu Guangwei,Pan Lanjia,Li Chunxing,You Futian,Wang Yin

Antibiotics residues in aqueous environment and sewage sludge accumulation have become serious environmental issues. The aim of this study is to investigate the potential of ciprofloxacin (CIP) removal by sludge-based biochar prepared from co-pyrolysis of sewage sludge and bamboo waste (BW). The stability and environmental risk of heavy metals (HMs) in the biochar were further investigated to evaluate potential risks for biochar utilization. Results showed that BW was an outstanding additive to prepare co-pyrolyzed biochar from sludge. A higher CIP removal rate (95%) of BW-sludge biochar (SBC) was obtained under initial CIP concentration of 10 mg/L, and its maximum adsorption capacity was 62.48 mg/g which was calculated from the Langmuir model. The pseudo-second-order and Freundlich model also well fit the CIP adsorption process, indicating a chemical and multilayer adsorption of CIP on a heterogeneous surface of biochar. Adsorption mechanism analysis indicated that the diverse functional groups and Fe species in biochar probably were the dominant factors in the adsorption of CIP. The π-π interaction, H–bond, ion exchange, and Fe-complexation might be the main interactions between the functional species and CIP molecules. Besides, HMs, especially the Cr, Cd, and As, were well immobilized in SBC compared with pure sludge biochar. This work suggested that sludge-based biochar, especially the co-pyrolyzed SBC, could be a potential adsorbent for CIP removal from aqueous solutions.

CAS / MDL: 85721-33-1
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Synergistic removal of aqueous ciprofloxacin hydrochloride by water surface plasma coupled with peroxymonosulfate activation

Weijie Hua,Yong Kang,Shuai Liu

A novel method of water surface plasma (WSP) combined with peroxymonosulfate (PMS) was developed for synergistic degradation of aqueous ciprofloxacin hydrochloride (CIP). The synergistic effect between WSP and PMS was demonstrated with the synergistic factor of 3.224. The CIP removal efficiency of the synergistic system was up to 96.6 % after 30 min of treatment, corresponding to the kinetic constant of 0.113 min −1 . The degradation performance experiments revealed that the PMS dosage of 6.4 mM, air flow rate of 0 L/min, peak voltage of 23 kV, initial pH and initial CIP concentration of acidic and 20 mg/L, respectively, were favorable for CIP removal. The combined system could maintain high removal efficiency (93.9 %) for the treatment of wastewater with high initial conductivity (950 μS/cm). OH, SO 4 − , O 3 , O 2 − and high-energy electrons were the active species responsible for CIP degradation, among which OH was the main active factor. UV–vis spectra and three-dimensional fluorescence spectra demonstrated the efficient removal of CIP. Possible degradation pathways and synergistic degradation mechanism were summarized. PMS was probably activated by O 3 , ultraviolet light and high-energy electrons generated in WSP. The presence of Cl − , SO 4 2− and HCO 3 − had a certain negative effect on CIP degradation in the WSP + PMS system, while HA had little effect on the final removal of CIP. The WSP + PMS degradation method has the advantages of high efficiency, high rate and low energy consumption compared with the previous literatures.

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International Journal of Electrochemical Science · 2023 · IF 1.5

Development of a molecularly imprinted photoelectrochemical sensor for enhanced detection of ciprofloxacin in milk

Qinghong Pan,Youyuan Peng,Ailing Yang,Da-peng Yang

In this work, a molecularly imprinted polymer (MIP)-based photoelectrochemical (PEC) sensor for the detection of ciprofloxacin (CIP) was constructed. Carbon-modified ZnO (ZnO/C) nanocomposite with adjustable zinc content was prepared by a carbonaceous method, facilitating visible light absorption and electron transition. The structure, morphology, and surface chemistry of ZnO/C were well characterized. The MIP membrane was formed by electropolymerizing, with ZnO/C nanocomposite, o-phenylenediamine (C 6 H 4 (NH 3 ) 2 ,o-PD), and CIP as highly efficient photoactive materials, functional monomer, and template, respectively. The PEC properties of different photoactive electrodes were measured and analyzed. The MIP-based PEC sensor showed excellent sensitivity and selectivity towards CIP, displaying a broad linear range from 0.01 nM to 1000 nM, a low detection limit of 8.41 pM, and satisfied recovery rates within 96.8% 103.2%. The sensor exhibited reliable reproducibility and stability, with a relative standard deviation (RSD) of 2.48% for the CIP in milk. The constructed MIP-based PEC sensor not only provides a powerful and reliable route for the detection of CIP, but also can be extended to detect other antibiotics in food and natural environment.

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Surfaces and Interfaces · 2023 · IF 6.2

Fabrication of Bi/BiOCOOH/PVDF with improved photocatalytic activity for the degradation of ciprofloxacin

Yue Shen,Haoyang Xu,Yage Zheng,Yao Wang,Liang Zhang,Zhiqiang Zhang,Lvling Zhong,Zhixian He

The development of a low-cost and recyclable method for wastewater treatment has been a major challenge. Polyvinylidene fluoride (PVDF) membranes have received considerable attention owing to their excellent mechanical strength , unique antioxidant properties, and low cost. In this study, Bi/BiOCOOH/PVDF composite membrane materials were prepared using a simple two-step solvent thermal method and phase conversion method. The results showed that under the synergistic action of adsorption and photocatalysis , the photocatalytic degradation efficiency of Bi/BiOCOOH composite material and Bi/BiOCOOH/PVDF composite membrane material for ciprofloxacin (CIP) was much higher than that of BiOCOOH. The introduction of PVDF acted as a carrier, improved the adsorption of the catalytic material to CIP, and facilitated the effective collision of the photocatalytic active site and CIP. The experimental results and theoretical calculations confirmed that the combination of Bi and BiOCOOH effectively improved the light absorption capacity and photocatalytic performance. The reproducibility test revealed that the small amount of new composite catalyst for Bi/BiOCOOH/PVDF as a carrier was lost and that the Bi/BiOCOOH/PVDF catalyst still had high catalytic activity. In addition, the influence of water matrix factors, such as pH and anion, on the photocatalytic degradation experiment was investigated, which would provide some reference for the actual wastewater treatment of the composite catalyst. This study demonstrates a photocatalytic activation mechanism between metals and semiconductors and provides some basis for constructing catalysts for the synergistic and effective treatment of water pollution through a combined adsorption and photocatalysis process.

CAS / MDL: 107-21-1 56-81-5
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Frontiers in Bioengineering and Biotechnology · 2023 · IF 5.7

Stability performance analysis of Fe based MOFs for peroxydisulfates activation to effectively degrade ciprofloxacin

Fang-Lan Geng,Hai-Yuan Chi,Hua-Chao Zhao,Jin-Quan Wan,Jian Sun

Fe-based metal-organic frameworks (MOFs) show high activity toward the activation of peroxodisulfate (PDS) for the removal of organic micropollutants (OMPs) in wastewater treatment. However, there is a phenomenon of Fe ion dissolution in the Fe-based MOFs’ active PDS system, and the reasons and influencing factors that cause Fe ion dissolution are poorly understood. In this study, we synthesized four types of Fe-based MOFs and confirmed their crystal structure through characterization. All types of Fe-based MOFs were found to activate PDS and form sulfate radicals (SO 4 − ), which effectively remove OMPs in wastewater. During the process of Fe-based MOFs activating PDS for CIP removal, activated species, oxidant reagent, and pH negatively impact the stability performance of the MOFs’ structure. The coordination bond between Fe atom and O atom can be attacked by water molecules, free radicals, and H + , causing damage to the crystal structure of MOFs. Additionally, Fe (II)-MOFs exhibit the best stability performance, due to the enhanced bond energy of the coordination bond in MOFs by the F ligands. This study summarizes the influencing factors of Fe-based MOFs’ damage during PDS activation processes, providing new insights for the future development of Fe-based MOFs.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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JOURNAL OF MOLECULAR STRUCTURE · 2023 · IF 3.8

Polyoxometalates as highly efficient adsorbents for ciprofloxacin removal: The key role of oxygen vacancies

Hao Zhang,Pengfei Zhang,Zhiliang Liu,Chunfang Du

In this study, various silver phosphomolybdates ( x - y - z -AgPMo) with oxygen vacancies were successfully prepared through H 2 calcination and subsequent chemical precipitation and used for the adsorption of ciprofloxacin (CIP) in water. The microstructures of x - y - z -AgPMo were analyzed by a series of characterization methods. The effects of calcination time, calcination temperature, hydrogen flow rate, and external adsorption conditions on the adsorption performance were investigated. The results showed that the adsorption performance of 1–0.1–250-AgPMo toward CIP could reach 91% within 20 min with a maximum adsorption capacity of 45.5 mg∙ g   −   1 , which was about 1.7 times as that of silver phosphomolybdate (Y-AgPMo) without H 2 calcination. The improved adsorption performance of 1–0.1–250-AgPMo was mainly attributed to the presence of oxygen vacancies, which induced more negative surface charges and larger specific surface area in 1–0.1–250-AgPMo. This work provided an excellent adsorbent for CIP removal and forcefully confirmed the important role of oxygen vacancies in the adsorption process.

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Journal of Cleaner Production · 2023 · IF 11.1

Natural wood-derived charcoal embedded with bimetallic iron/cobalt sites to promote ciprofloxacin degradation

Shuqiang Pang,Chengfeng Zhou,Yuanyuan Sun,Kewei Zhang,Wanneng Ye,Xiaoliang Zhao,Liping Cai,Bin Hui

Structural design of high-performing catalysts for boosting refractory organic pollutants degradation remains a great challenge. Herein, a natural wood-derived catalyst comprising of wood carbon and Fe/Co sites was proposed as the peroxymonosulfate (PMS) activator to enhance ciprofloxacin (CIP) pollutant degradation. The bimetallic Fe/Co sites were highly dispersed and stabilized on carbon surface. The carbon-based catalyst achieved 100% removal rate for CIP within 4 min. After four consecutive cycles, the removal rate still reached 92.8%, displaying separable and reusable ability of this catalyst. The carbon-based catalyst could also exhibit excellent degradation performance under a wide pH range of 2.0–8.0. Density functional theory (DFT) calculation revealed that Fe/Co sites at wood carbon had the high adsorption energy and induced interfacial electron transfer for enhanced breakage of O–O bond. The sulfate radical (SO 4 •− ), hydroxyl radical (•OH) and singlet oxygen ( 1 O 2 ) were main reactive oxygen species and their relative contribution was calculated to be 13.51%, 17.54% and 68.95%, respectively. The formed by-products and intermediates had almost no toxicity. This work proposes a new structural design of wood carbon-based system for enhancing antibiotic pollutant in aqueous environment, which facilitates the development of wastewater treatment technology.

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Environmental Technology & Innovation · 2023 · IF 7.1

Removal of heavy metals lead and ciprofloxacin from farm wastewater using peanut shell biochar

Xinyue Li,Tonglinxi Liu,Xing Han,Yilin Li,Xiulan Ma

In this paper, peanut shells were used as the raw material for preparing biochar (PBC), and artificial simulated aging was used to age the PBC. To investigate the effectiveness of biochar before and after aging for the removal of Pb and ciprofloxacin (CIP) alone and the feasibility of simultaneous removal of Pb and CIP. The effects of different aging methods on the physicochemical properties of biochar were investigated by measuring the specific surface area (BET), scanning electron microscopy (SEM), X-ray diffraction (XRD) and Fourier transform infrared absorption spectrometry (FTIR) of biochar. The results showed that the C content of biochar decreased after aging, while the O/C, H/C, (N+O)/C, and O contents increased. Kinetic adsorption, adsorption isothermal and competitive adsorption experiments were performed to study the adsorption properties of CIP and Pb 2 + 2+ by aging biochar under single and combined pollution systems. Aging inhibited the adsorption of ciprofloxacin on biochar, and the inhibition size was ranked as high-temperature aging > freeze-thaw cycles aging > natural aging. However, the effect of aging on the adsorption of Pb 2 + 2+ by biochar was insignificant. Pb 2 + 2+ in the complex contamination system would compete with CIP for oxygen-containing functional groups and adsorption sites on biochar, indicating that the pollutant adsorption mechanism by biochar is complex and influenced by various factors such as aging methods and pollutant species. This study shows that regional climatic factors and target pollutant species must be considered when applying biochar for pollutant removal , which may affect the long-term effects of pollution remediation.

CAS / MDL: 85721-33-1 10099-74-8
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ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY · 2018 · IF 3.974

Novel alginate particles decorated with nickel for enhancing ciprofloxacin removal: Characterization and mechanism analysis

Xiaonuo Zhang,Xiaoyan Lin,Hanlin Ding,Yu He,Hao Yang,Yan Chen,Xiaoyan Chen,Xuegang Luo

The extensive occurrence of antibiotics (such as ciprofloxacin) in aqueous environment had raised severe concerns due to their impacts on humans and the ecosystem. In this study, a novel nickel alginate particles adsorbent had been successfully developed by combining an alginate matrix with nickel ion through immobilization and crosslinking technology and then was applied for the batch adsorption study of ciprofloxacin to evaluate its potential performance. The as-prepared adsorbent exhibited excellent adsorption performance at the condition of the pH 7 and 328.15 K, and the results indicated that the maximum adsorption capacity was 135.18 mg g −1 . The isotherm and kinetic studies were well fitted to the Langmuir and pseudo-second-order models, respectively. A thermodynamics analysis displayed that the ciprofloxacin adsorption process was endothermic, feasible and spontaneous. The as-prepared adsorbent before and after adsorption was characterized through SEM, EDX and XPS analyses, and the particle size of the as-prepared adsorbent was roughly 914 µm. Hydrogen bond , the cation bonding bridge and n-π electron-donor-acceptor interaction might be the driving force of the ciprofloxacin adsorption process. This study demonstrated that this as-prepared adsorbent was a promising and efficient material for the ciprofloxacin adsorption from the aqueous solution.

CAS / MDL: 85721-33-1 9005-38-3
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2018 · IF 2.891

Ciprofloxacin degradation in UV/chlorine advanced oxidation process: Influencing factors, mechanisms and degradation pathways

Jia Deng,Guangxue Wu,Shoujun Yuan,Xinmin Zhan,Wei Wang,Zhen-Hu Hu

Ciprofloxacin (CIP) is a widely used third generation fluoroquinolone antibiotics, and has been often detected in wastewater treatment plants. Finding an effective way to remove them from wastewater is of great concern. Ultraviolet (UV)/chlorine advanced oxidation process (AOP) has many advantages in micropollutant removal. In this study, CIP degradation in UV/chlorine process was investigated. Only 41.2% of CIP was degraded by UV photolysis and 30.5% by dark chlorination in 30 min, while 98.5% of CIP was degraded by UV/chlorine process in 9 min. HCO 3 − had markedly inhibition, NO 3 − and SO 4 2- had slight inhibition, and Cl − had a marginal inhibition on CIP degradation in UV/chlorine system. The degradation of CIP in UV/chlorine process was mainly attributed to the attack of reactive species. The relative contributions of hydrated electrons (e aq ), hydroxyl radicals (HO ), chlorine atoms (Cl ), and UV photolysis were investigated. Under neutral condition in aqueous solution, CIP degradation had highest pseudo first-order reaction rate constant, in which e aq had the highest contribution, followed by Cl , HO , and UV photolysis. The intermediates and byproducts were identified and the degradation pathway was proposed. The total organic chlorine (TOCl) and biotoxicity were further assessed. CIP and natural organic matters (NOMs) were removed efficiently in real water. UV/chlorine showed the potential for the wastewater treatment containing CIP.

CAS / MDL: 7681-52-9 75-65-0
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JOURNAL OF SEPARATION SCIENCE · 2018 ·Vol. 41 ·期 19 ·3782-3790 · IF 2.415

Fluorescent molecularly imprinted nanoparticles for selective and rapid detection of ciprofloxacin in aquaculture water

Chunxia Wu,Rujia Cheng,Jixiang Wang,Yunyun Wang,Xuan Jing,Rongru Chen,Lin Sun,Yongsheng Yan

Fluorescent molecularly imprinted nanoparticles have shown great promise in the field of chemical analysis or detection because of their high stability, selectivity, and sensitivity. In this work, fluorescent molecularly imprinted nanoparticles were synthesized by precipitation polymerization employing fluorescein isothiocyanate as luminescent material, which could efficiently and rapidly detect ciprofloxacin in water samples. The prepared fluorescent molecularly imprinted nanoparticles had remarkable stability and good selectivity with the method detection limit low to 4.04 nm. In addition, the fluorescent-imprinted nanoparticles were capable of identifying the target with high detection efficiency and were applied to the detection of ciprofloxacin in aquaculture water with complex composition. All these would provide the direct monitoring of ciprofloxacin in environmental water with a promising fluorescent imprinting strategy.

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NEW JOURNAL OF CHEMISTRY · 2024 ·Vol. 48 ·期 20 ·9185-9195 · IF 2.7

Construction of an MIL-101(Fe)/layered bimetallic oxide heterojunction for enhanced ciprofloxacin removal

Shikai Xue,Dongying Zhu,Qing Zuo,Shuangfeng Yang,Haiyan Wang,Qiujun Lu,Guoxing Yin,Guihua Ruan,Fuyou Du

A novel MIL-101(Fe)/ZnCrZr-LBMO heterojunction was successfully constructed and used for the removal of ciprofloxacin (CIP) in this work. The MIL-101(Fe)/ZnCrZr-LBMO composite exhibited significantly enhanced photocatalytic degradation activity, with reaction rates approximately 3.4 and 3.1 times faster than those observed with pristine MIL-101(Fe) and ZnCrZr-LBMO, respectively. The effect of different amounts of ZnCrZr-LBMO, sample pH, CIP concentration, inorganic cations, and anions on CIP removal was investigated, and the possible intermediates and degradation pathways of CIP were speculated. The·O2− radicals dominated CIP degradation, with minor contributions from 1O2, h+, and ·OH radicals. The composite exhibited high removal rates for CIP (94.7%), ofloxacin (86.8%), and tetracycline (96.3%), respectively, within 60 min of light irradiation, and excellent reusability, retaining over 85.1% CIP degradation rate after five cycles. Our work provides a new reference to construct highly efficient and easily recyclable MIL-101(Fe)/ZnCrZr-LBMO photocatalysts for the removal of antibiotic pollutants, promising advancements in real water treatment applications.

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