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JOURNAL OF APPLIED MICROBIOLOGY · 2016 ·Vol. 121 ·期 6 ·1616-1626 · IF 2.156

Biodegradation of phenanthrene by Rhizobium petrolearium SL‐1

Huang X.,Shi J.,Cui C.,Yin H.,Zhang R.,Ma X.,Zhang X.

AimsWe aimed to investigate the phenanthrene degradation characteristics and possible phenanthrene degradation pathways of Rhizobium petrolearium SL‐1.Methods and ResultsUsing high‐performance liquid chromatography (HPLC), UV‐visible and gas chromatography‐mass spectrometry (GC‐MS) analysis, the phenanthrene‐degrading properties and metabolites of Rh. petrolearium SL‐1 were analysed, and then combined with genome‐based analysis to elucidate the possible biodegradation pathway of phenanthrene in Rh. petrolearium SL‐1. The results of the analyses showed that phenanthrene (100 mg l−1) was completely degraded by strain SL‐1 at 35°C, 0·02% salinity and pH 9·0 within 3 days. A wide range of polycyclic aromatic hydrocarbons, including naphthalene, fluorene, anthracene and pyrene, could also be degraded by this strain.ConclusionsBased on the identified metabolites, the utilization of probable intermediates and the presence of putative phenanthrene catabolic genes, we concluded that phenanthrene was degraded via two different routes, namely the ‘naphthalene’ and the ‘phthalic acid’ routes.Significance and Impact of the StudyFor the first time, this study shows the degradation pathway of phenanthrene by a Rhizobium strain. Because of its excellent stress resistance, metabolic versatility, high degradation efficiency and potential application in phytoremediation, Rh. petrolearium SL‐1 is a potential candidate for the bioremediation of polycyclic aromatic hydrocarbons‐contaminated areas.

研究领域: 环境微生物学 · 分子生物学 · 生态学
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Results in Engineering · 2025 · IF 7.9

Worm-mic-derived hierarch porous monos: Ultra SL uptake

Jiao Yan,Zhenzhen Li,Chengye Yang,Ke Xu,Ying Tang

A novel gel-templated strategy, featuring the unique employment of cationic worm-like micelles as a 3D gel template, was developed to fabricate hierarchically porous MgFe-layered double hydroxide (BTAC-MgFe-LDH) monoliths with ultra-high adsorption capacity toward sulfonated lignite (SL). Specifically, behentrimonium chloride (BTAC) and sodium salicylate self-organize into such cationic worm-like micelles, which serve as a 3D gel scaffold to mediate the co-precipitation of metal ions. After subsequent removal of this gel network, interconnected meso- and macropores (5–80 nm) are formed-these pores boost the specific surface area to 103.93 m² g⁻¹ (over double that of conventional LDH) and the pore volume to 0.63 cm³ g⁻¹ (four times higher than conventional LDH). For the resulting monolithic gel-derived adsorbent, 97.1% SL removal is achieved within 20 min at pH 3 and 25°C; its adsorption follows pseudo-second-order kinetics, with a Langmuir maximum capacity of 64.93 mg g⁻¹ (experimental result: 92.1 mg g⁻¹). Thermodynamic parameters (ΔH = - 21.08 J mol −1 ; ΔS = - 44.61 J mol −1 k −1 ) confirm spontaneous, exothermic adsorption dominated by electrostatic interactions and interlayer anion exchange. The BTAC-MgFe-LDH still retains over 64% of its capacity after five cycles, this result confirms that the gel-based approach provides a scalable, eco-friendly route to fabricate robust monolithic materials, which are effective at removing macromolecular organic pollutants from oilfield wastewater.

CAS / MDL: 17301-53-0 497-19-8
研究领域: 环境科学 · 材料化学 · 吸附技术 · 废水处理 · 功能材料
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2017 · IF 3.012

Enhanced performance of the electrolytes based on sulfolane and lithium difluoro(oxalate)borate with enhanced interfacial stability for LiNi0.5Mn1.5O4 cathode

Hongming Zhou,Demin Xiao,Chengjie Yin,Zhaohui Yang,Kaiwen Xiao,Jian Li

The electrolytes based on lithium difluoro(oxalate)borate (LiODFB) and sulfolane (SL) including LiODFB-ethylene carbonate (EC)/dimethyl carbonate (DMC) and LiPF 6 -EC/DMC as the references have been studied on electrochemical performance and interfacial stability in Li/LiNi 0.5 Mn 1.5 O 4 cells. LiODFB-containing electrolytes show outstanding electrochemical stability within 5.5   V due to the passivation phenomenon on the cathodes, while LiPF 6 -containing electrolytes undergo continuous decomposition beyond 4.5   V. The initial charge/discharge profiles and cyclic voltammetry (CV) curves prove that the cell with LiODFB-SL/DMC(2:1 by vol.) electrolyte has lower degree of polarization and better reversibility. The cathode with LiODFB-SL/DMC(2:1 by vol.) electrolyte displays the best cycling performance and the cathode with LiPF 6 -EC/DMC(1:1 by vol.) electrolyte displays the worst cycling performance. AC impedance shows that the cell cycling with LiODFB-SL/DMC(2:1 by vol.) electrolyte has much smaller resistance of charge transfer on cathode/electrolyte interface than the cell cycling with LiODFB-EC/DMC(1:1 by vol.) electrolyte. The characterization of the cathode surfaces indicates that a more homogeneous and compact passivation layer forms on the cathode cycling with LiODFB-SL/DMC(2:1 by vol.) electrolyte to greatly improve the interfacial stability for the reason that SL motivates the passivation reaction of LiODFB and itself participates the formation of the passivation layers. Therefore, LiODFB-SL/DMC(2:1 by vol.) is a promising electrolyte for LiNi 0.5 Mn 1.5 O 4 cathode.

研究领域: 材料科学 · 电化学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Lithium-selective extraction utilizing lithium-trap LiAlFe-LDHs/MWCNTs/QCS composite membrane within the ship lock-type ion selective permeability system

Yi Wang,Huanhuan Guo,Xiaohan Xing,Can Wang,Xuefeng Zhang,Xiumin Li,Fengfeng Gao,Xiaogang Hao

A lithium aluminum iron layered double hydroxides/multiwalled carbon nanotubes/quaternized chitosan (LiAlFe-LDHs/MWCNTs/QCS) composite membrane with lithium-ion vacancies (Li + -trap) was fabricated through vacuum filtration method and pre-desorption process. The Li + -trap LiAlFe-LDHs/MWCNTs/QCS composite membrane had been developed for the selective extraction of Li + within the ship lock-type ion selective permeability (SL-ISP) system. In the Li + -trap LiAlFe-LDHs/MWCNTs/QCS composite membrane, the Li + -trap within LiAlFe-LDHs was pivotal for achieving selective Li + extraction. This selectivity was realized through the cyclic intercalation of Li + into the Li + -trap sites within the interlayer structure of LiAlFe-LDHs, a process that also facilitates the permeation of Cl - . The interference of impurity ions was further eliminated by the SL-ISP system, thus facilitating the selective extraction of Li + . Upon investigation, the Li + -trap LiAlFe-LDHs/MWCNTs/QCS composite membrane was found to achieve a Li + flux of 0.055 mol·m −2 ·h −1 and a separation factor of 8.3 at an equimolar concentration ( C Mg, Li  = 0.05 M) within the SL-ISP system. Additionally, the Li + -trap LiAlFe-LDHs/MWCNTs/QCS composite membrane demonstrated excellent separation performance in simulated brine, with a calculated Li + permeation flux of 0.053 mol·m −2 ·h −1 . The separation factors of Li + /Mg 2+ , Li + /K + , Li + /Na + and Li + /Ca 2+ reached values of 91.84, 69.75, 81.51 and 17.99, respectively. Therefore, the Li + -trap LiAlFe-LDHs/MWCNTs/QCS composite membrane could be effectively applied in the SL-ISP system for the selective extraction of Li + .

CAS / MDL: 308068-56-6
研究领域: 材料科学 · 化学工程
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RSC Advances · 2020 ·Vol. 10 ·期 23 ·13830-13837 · IF 3.119

Synthesis of anti-photolysis lignin-based dispersant and its application in pesticide suspension concentrate

Ruifen Peng,Yuxia Pang,Xueqing Qiu,Yong Qian,Mingsong Zhou

In the formulation of pesticide Suspension Concentrate (SC), some photosensitive pesticides are easily decomposed in the preparation. In this study, a hindered amine modified lignosulfonate (SL-Temp) with anti-photolysis function was synthesized using 4-amino-2,2,6,6-tetramethylpiperidine (Temp) and Sodium Lignosulfonate (SL) to solve this problem. The obtained SL-Temp was used as a dispersant to prepare 5% SC of avermectin, which shows good physical stability. The decomposition rate of the avermectin in SC after accelerating hot storage is 0%, which is much lower than 6.1% when SL was used as the dispersant. After being exposed to UV irradiation for 60 hours, the highest retention rate of avermectin is 87.1% when SL-Temp was used as the dispersant, which is much higher than 73.6% when SL was used as the dispersant, and also higher than 76.3% when a small molecule antioxidant (BHT) was added to the formulation. QCM-D studies revealed that the SL-Temp adsorption layer on avermectin particles can compete to absorb partial ultraviolet rays, hinder the penetration of ultraviolet light, and scavenge the free radicals produced by photooxidation, so as to protect avermectin from degradation.

研究领域: 农药科学 · 材料化学
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Sensor Letters · 2016 ·Vol. 14 ·期 11 ·1067-1073 · IF 0

A Novel Sensitive Electrochemiluminescence Method for Determination of Tetracaine Hydrochloride Based on ZnO/RGO Modified Electrode

Wu Wenwen,Wang Sui

In this work, we reported a luminol electrochemiluminescence (ECL) sensor using a composite material compounded by ZnO nanoparticles and reduced graphene oxide (ZnO/RGO) as electrode membrane and in situ generated hydrogen peroxide as coreactant. The composite material was characterized by fourier transform infrared spectroscopy analysis (FTIR) and X-Ray powder diffraction (XRD). Then this ZnO/RGO modified electrode was used to determine tetracaine hydrochloride (TA· HCl). Results show that the inhibition of ECL intensity increased with logarithm of TA · HCl concentration within a linear range from 10–4 μg/mL to 10–2 μg/mL and the detection limit (S/N) was 3.3 × 10–5 μg/mL. In addition, the recoveries of real samples were 85.0%–104.0% (urine), 95.0%–127.4% (serum) and 87.0%–104.6% (raw material drug) respectively, demonstrating an acceptable reproducibility of this method.

研究领域: 分析化学 · 药物分析
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Sensor Letters · 2017 ·Vol. 15 ·期 8 ·682-689 · IF 0

Electrochemical Deposition of Graphene Films for Cr(VI) Fast Detection in Water

Li Yueqi,Hu Jingfang,Zou Xiaoping,GuoweiGao

In this paper, a simple and highly sensitive sensing interface of graphene film for hexavalent chromium (Cr(VI)) determination has been prepared by controllable electrochemical deposition on the gold electrode surface. The graphene film was obtained by direct electroreduction of graphene oxide (GO) in suspension solution. The investigations on deposition parameters of this controllable preparation, such as potential and deposition time, were carried out by the potentiostatic method to study the effects of them on the graphene film. The fabrication process and electrochemical properties of graphene film were characterized by scanning electron microscope (SEM), transmission electron microscope (TEM) and electrochemical techniques, respectively. The conditional parameters, including detection potential, the concentration of supporting electrolyte and pH, were optimized for Cr(VI) analysis. Without preconcentration, chronoamperometry method was used for Cr(VI) fast detection. Under the optimized conditions, the graphene film modified electrode provided a fast detection process, a wide linear range from 5 μg/L to 2000 μg/L, and a low detection limit of 0.5 μg/L (S/N ≥ 3). Also, the developed graphene film showed a good stability and anti-interference for Cr(VI) determination. The reported work holds promise for practical application due to its simple, fast, environment-friendly and economical natures.

研究领域: 环境科学 · 分析化学
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Sensor Letters · 2016 ·Vol. 14 ·期 9 ·859-863 · IF 0

The Synthesis of PtFe/C and Its Application in Non-Enzymatic Glucose Sensor

Ding Yu,Li Yibin,Wu Huimin,Wang Shengfu,Xia Qinghua

20 wt% PtFe/C catalysts were prepared by a chemical reduction method at high temperature. The catalysts were characterized by X-ray diffraction, transmission electron microscopy, and electrochemical testing. The sensor based on PtFe/C showed a detection limit of 0.03 mM and high sensitivity with linear range from 0.1 mM to 13.5 mM. The sensor still had high selection for glucose in the presence of commonly interfering species, such as ascorbic acid, acetamidophenol, and uric acid. The as-prepared glucose sensor has good anti-interference performance.

研究领域: 材料科学 · 电化学 · 生物传感
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Sensor Letters · 2016 ·Vol. 14 ·期 4 ·369-375 · IF 0

The High Sensitivity NO2 Surface Acoustic Wave Sensor with New Sensing Film Made by a Novel Method

Youwang Hu,Chengzhi Xu,Ji'an Duan,Jiwen Xiang,Shu Wang,Xiaoyan Sun

Surface Acoustic Wave (SAW) sensors have received great attention because of their compact design and excellent sensing performance, including high sensitivity, low detection limits. However, SAW sensors generally suffer from low quality of the solid thin films which has a significant effect to the detection performance of the sensors. To solve this problem, three different methods (spin coating, drop coating and spray coating) for fabricating thin films have been investigated for gaseous nitrogen dioxide (NO2) SAW sensors in this work. Spray coating method showed its advantages in improving the solid film quality of the sensing layer and the performance of the sensors. SEM characterization shows that the spray coating films are more uniform and poly-porous. Sensors with spray coating film can detect NO2 range from sub ppm to hundreds ppm with high sensibility and stability. Its sensitivity is 42.31 Hz/ppm and its sensing limit is down to 57.2 ppb.

研究领域: 材料科学 · 环境监测 · 传感器技术
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Sensor Letters · 2016 ·Vol. 14 ·期 7 ·656-664 · IF 0

Hydrogen Peroxide Biosensor Based on Polypyrrole-Fullerene-DDAB Nanocomposite Film

Dong Yan,Wang Lu,Nie Fei,Zheng Jianbin

A novel polypyrrole-fullerene-didodecyldimethylammonium bromide (PPy-C60-DDAB) was synthesized by an in situ chemical oxidative polymerization method. Scanning electron microscopy (SEM) study showed the morphologies of the nanocomposites. The direct electrochemistry of hemoglobin (Hb) immobilized on the designed PPy-C60-DDAB composite film modified carbon ionic liquid electrode (Nafion/Hb/PPy-C60-DDAB/CILE) and its biosensing for hydrogen peroxide (H2O2) were investigated. The results indicated that direct electron transfer of Hb was realized on the underlying electrode with the usage of the PPy-C60-DDAB nanocomposite film. Moreover, the Nafion/Hb/PPy-C60-DDAB/CILE based sensor showed prominent electrocatalytic activity for the detection of H2O2. The current response was linearly related to the H2O2 concentration in the range from 1 to 114 μM, with a sensitivity of 936 μA mM–1 cm–2 and a second range from 114 to 1479 μM with a sensitivity of 299 μA mM–1 cm–2. The detection limit was 0.3 μM at a signal-to-noise ratio of 3. Thus the PPy-C60-DDAB composite provided by simple synthesis technique will have potential application in studying the electron transfer of enzyme and the design of novel electrochemical biosensors.

研究领域: 材料科学 · 电化学 · 纳米技术 · 生物传感器 · 分析化学
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Sensor Letters · 2016 ·Vol. 14 ·期 11 ·1161-1167 · IF 0

Synthesis of Novel Nanostructures of CuO, Their Characterization and Potential Applications for the Amperometric Detection of Dopamine

Ibupoto Zafar Hussain,Tahira Aneela,Mallah Arfana Begum,Willander Magnus,Yu Cong

In this investigation, novel nanostructures of CuO are synthesized by hydrothermal method using biotemplates. The CuO nanomaterial was characterized by various analytical techniques such as scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). These techniques showed well controlled morphology, excellent crystalline quality, and high purity in chemical composition. The glassy carbon electrode was modified with these CuO nanostructures for the electrochemical determination of dopamine. The electrochemical response of modified electrodes was measured by cyclic voltammetry and amperometric techniques. The CuO nanostructures had shown excellent catalytic activity towards the oxidation of dopamine. The presented dopamine biosensor exhibits wide linear range of dopamine concentrations, low limit of detection, sensitive, selective and reproducible features. The linear range for the CuO nanostructures based dopamine biosensor falls in the range of 25 to 870 μM and limit of detection was found 0.1 μM. There was found negligible response for common interferents such as ascorbic acid, uric acid, and glucose. Finally, the proposed dopamine biosensor was potentially applied for the quantification of dopamine from real samples and the obtained results are very satisfactory. This study provides the solid route for other applications of CuO based on its improved catalytic properties.

研究领域: 材料科学 · 分析化学 · 生物医学工程
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Sensor Letters · 2014 ·Vol. 12 ·期 10 ·1462-1468 · IF 0.558

Highly Sensitive Electrochemical Biosensing of Phoxim Pesticide Based on Ionic Liquid-Functionalized Graphene as Modifier

Liu Zhi-Min,Zheng Ying-Ying,Jing Yan-Feng,Li Jie,Zhan Hai-Jun,Shen Qi

A facile, one-step synthesis of ionic liquid-functionalized graphene (IL-GR) nanocomposite using graphene oxide (GO) and amine-terminated ionic liquid (NH2-IL) was first presented through an epoxide ring-opening reaction, then acetylcholinesterase (AChE) was immobilized onto IL-GR nanocomposite film modified glassy carbon electrode to prepare a highly sensitive AChE biosensor. The morphologies and electrochemistry properties of the composite were investigated by using scanning electron microscopy, transmission electron microscopy and cyclic voltammetry, respectively. The nanocomposite not only provided a biocompatible microenvironment to keep the bioactivity of AChE, but also exhibited a strong synergetic effect on improving the sensing properties of phoxim. The immobilized AChE showed favorable affinity to acetylthiocholine (ATCl) and could catalyze the hydrolysis of ATCl with a Kapp m value of 0.143 mM. The proposed biosensor exhibited a detection limit of 6.0 × 10–11 M (S/N = 3) towards phoxim. Besides, the biosensor is easy to prepare, have good stability, and will have potential application in organophosphate pesticides.

研究领域: 分析化学 · 环境科学 · 生物技术
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