Chemical Engineering Journal Advances
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2022
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IF 0
Hiu Lam So,Wei Chu
Degradation of 1-Naphthol by combined photocatalysis and adsorption in column reactor was studied, and the performance could be predicted by employing a proposed multiple regression model. The model includes four variables: concentration of 1-Naphthol, concentration of peroxymonosulfate (PMS), FeOOH dosage and pH, along with their second-order effects and interactions. Statistical analyses were performed to verify the statistical significance of the regressors, and extra experimental sets were conducted to validate the proposed model. The mathematical model proposed exhibited good reproducibility with no significant statistical difference between the experimental and predicted values. Response surface methodology was used to explore the relationship between the four variables and the response. The process optimal ranges can be further refined at pH 2–2.5; [PMS] = 1.2–1.4 mM; and FeOOH 2.75–3 g respectively, according to the proposed overlaid contour plots.
研究领域:
环境科学
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化学工程
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DOI
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
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2020
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IF 4.192
Yidong Zhou,Zhijian Ke,Hangting Ye,Mengting Hong,Yifei Xu,Mingliang Zhang,Wankui Jiang,Qing Hong
Carbaryl is a widely used carbamate pesticide in agriculture. The strain Rhizobium sp. X9 possesses the typical carbaryl degradation pathway in which carbaryl is mineralized via 1-naphthol, salicylate, and gentisate. In this study, we cloned a carbaryl hydrolase gene cehA and a novel two-component 1-naphthol hydroxylase gene cehC1C2. CehA mediates carbaryl hydrolysis to 1-naphthol and CehC1, an FMNH2 or FADH2-dependent monooxygenase belonging to the HpaB superfamily, and hydroxylates 1-naphthol in the presence of reduced nicotinamide-adenine dinucleotide (FMN)/flavin adenine dinucleotide (FAD), and the reductase CehC2. CehC1 has the highest amino acid similarity (58%) with the oxygenase component of a two-component 4-nitrophenol 2-monooxygenase, while CehC2 has the highest amino acid similarity (46%) with its reductase component. CehC1C2 could utilize both FAD and FMN as the cofactor during the hydroxylation, although higher catalytic activity was observed with FAD as the cofactor. The optimal molar ratio of CehC1 to CehC2 was 2:1. The Km and Kcat/Km values of CehC1 for 1-naphthol were 74.71 ± 16.07 μM and (8.29 ± 2.44) × 10–4 s–1·μM–1, respectively. Moreover, the enzyme activities and substrate spectrum between CehC1C2 and previously reported 1-naphthol hydroxylase McbC were compared. The results suggested that McbC had a higher 1-naphthol hydroxylation activity, while CehC1C2 had a broader substrate spectrum.
研究领域:
环境微生物学
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生物化学
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农药生物降解
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DOI
PubMed
高影响因子
DESALINATION
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2020
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IF 7.098
Md Mofasserul Alam,Masem Hossain,Ying Mei,Chenxiao Jiang,Yaoming Wang,Chuyang Y. Tang,Tongwen Xu
Anion exchange membrane (AEM) as a positively-charged polymer allows the transition of anions, block the cations, and has been widely used in the electro-desalination processes. Permselectivity , alkaline stability, and electric ohmic resistance on the AEM are critical issues determining the final desalination efficiency in an electro-desalination process. Here in this work, the AEM with sound desalination and alkaline stable character was fabricated from the aspect of functional group optimization, i.e., introduce into the 2, 6-dimethyl-1, 4-phenylene oxide (PPO) polymer matrix as the alternative of the conventional. The 1-naphthol derivatives, i.e., 2-[dimethylaminomethyl] naphthalen-1-ol, and 2,7-bis[dimethylaminomethyl] naphthalen-1-ol as the functional groups provide conjugated π-electron, which may increase the alkaline stability of the anion exchange membranes (AEMs), and thus guarantee its long-term stability when operating the electro-desalination process over the limiting current density condition. The innovative membranes perform lower area resistance 0.5–2.27 Ω cm 2 and well stability in the alkaline circumstance. In comparison to the commercial membranes (Neosepta AMX, standard grade), the obtained membrane presented comparable electro-desalination performance. The results indicate AEMs that functionalized by 1-naphthol derivatives can be a promising candidate for electro-desalination processes.
研究领域:
材料科学
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环境工程
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DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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2019
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IF 3.218
Wei Chen,Jiayue Dong,Sihan Zhou,Chunyong Zhang,Degang Fu
1-naphthol (1-NAP) and 2-naphthol (2-NAP) are both hazardous pollutants which pose great threat to our living environment. In the current work, a comparative investigation on the electrochemical mineralization of 1-NAP and 2-NAP using boron-doped diamond (BDD) anode was presented. Experiments were carried out using synthetic 1-NAP or 2-NAP solutions containing Na 2 SO 4 as supporting electrolyte . A two-level factorial design methodology was adopted to optimize the mineralization process, six mathematical models were thus constructed and used to explore the structure-property relation involved. The results obtained suggested that 1-NAP was easier and faster to break down than 2-NPA under the same oxidation conditions, which were in line with the outcome obtained from cyclic voltammetry , HPLC and TOC measurements. To understand the destruction mechanism, the electron structures of 1-NAP and 2-NAP were further examined by the quantum chemistry calculations with density functional theory. It was also found that the results from frontier orbital analysis could well explain the differing mineralization performances recorded in BDD anode cell. Finally, with the aid of LC/MS analysis, the oxidation pathways of 1-NAP or 2-NAP on BDD anodes were proposed.
研究领域:
环境科学
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电化学
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DOI
高影响因子
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY
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2020
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IF 4.872
Zi-Jian Chen,Xi-Xia Liu,Zhi-Li Xiao,Hui-Jun Fu,Yu-Ping Huang,Shu-Yi Huang,Yu-Dong Shen,Fan He,Xing-Xing Yang,Bruce Hammock,Zhen-Lin Xu
1-naphthol (1-NAP) is the main metabolite of pesticide carbaryl and naphthalene , and is also a genotoxic and carcinogenic intermediate in the synthesis of organic compound, dyes, pigment and pharmaceutical industry . In this work, two novel haptens were designed and synthesized for developing a competitive indirect enzyme-linked immunosorbent assay (ciELISA) method for 1-NAP in urine samples. The assay showed a limit of detection of 2.21 ng/mL and working range from 4.02 ng/mL to 31.25 ng/mL for 1-NAP in optimized working buffer. The matrix effect of samples was eliminated via 15-fold dilution of optimized working buffer. Good average recoveries (102.4%–123.4%) with a coefficient of variation from 11.7% to 14.7% was obtained for spiked urine samples. Subsequent instrument verification test showed good correlation between the results of ciELISA and high-performance liquid chromatography . The developed ciELISA is a high-throughput tool to monitor 1-NAP in urine, which can provide technical support for the establishment of biological exposure level for the exposure to carbaryl, naphthalene and other related pollutants.
研究领域:
环境生物学
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毒理学
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分析化学
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DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2015
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IF 4.321
Jun Wang,Baoliang Chen
The adsorption and coadsorption of naphthalene, 1-naphthol and Cd 2+ onto graphene oxide (GO), chemically reduced graphene (CRG) and annealing reduced graphene (ARG) were compared to determine the unique adsorption properties of graphene nanosheets. The adsorption capability of organic pollutants followed the order CRG > ARG > GO, and all three adsorbents showed stronger adsorption to 1-naphthol than to naphthalene. In addition to a π–π interaction, the strong adsorption of 1-naphthol onto graphene nanosheets was mainly attributed to the n –π electron-donor–acceptor (EDA) interactions between the –OH groups of 1-naphthol and the electron-depleted sites on graphene nanosheets. The adsorption of 1-naphthol on reduced graphene materials increased with increasing pH and reached a maximum around its pKa, supporting the n –π EDA interaction mechanism. GO with more functional groups on the nanosheets over CRG and ARG exhibited a strong affinity with Cd 2+ . The adsorption of Cd 2+ onto GO and CRG facilitated the coadsorption of naphthalene and 1-naphthol via surface-bridging mechanisms, such as cation–π interactions. Notably, though ARG showed no significant Cd 2+ adsorption, the suppressed coadsorption of naphthalene onto ARG may be attributed to the sieving effect by hydrated Cd 2+ binding to the micropore edges on ARG.
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
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2015
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IF 4.321
Ziwei Zhang,Fang Wang,Weiben Yang,Zhen Yang,Aimin Li
In this study, a novel macroporous amination resin (named as GMDA) with the matrix of divinylbenzene and glycidyl methacrylate was synthesized and utilized to remove 8-amino-1-naphthol-3,6-disulfonic acid (H-acid) from water. The adsorption behaviors of the synthetic resin were studied systematically and compared with three commercial resins (the hypercrosslinked resin NDA-88, the anion-exchange resin D-301, and the macroporous resin XAD-4) in terms of adsorption capacity, equilibrium time, isotherm adsorption , the effect of existing inorganic ions and regeneration properties. The characteristic methods of BET surface area, pore size distribution, SEM , FTIR , XPS and Zeta potential were investigated to analyze the resins and adsorption process . The GMDA resin has wider pore diameter than the NDA-88 resin to attract H-acid more quickly with higher adsorption amounts; the larger BET surface area of the GMDA resin ensures more binding sites than the D-301 resin in the adsorption process; the functional groups on the surface of the GMDA resin is more effective than the hydrophobic matrix of the resin XAD-4 in the removal of H-acid. Especially, the regeneration and dynamic experiments indicate the anti-fouling performance of GMDA resin is much better than the others. This research not only provides guidance for understanding the adsorption mechanism of H-acid onto the four resins, but also gives theoretical basis for the design of resin structure according to the targeted contaminants.
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
高影响因子
JOURNAL OF CHROMATOGRAPHY A
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2016
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IF 3.926
Qingxiang Zhou,Man Lei,Jing Li,Kuifu Zhao,Yongli Liu
Magnetic Fe@MgAl-layered double hydroxides (MgAl-LDHs) composite was firstly synthesized by coating MgAl-layered double hydroxides on the surface of the dispersed nanoscale zero valent irons with co-precipitation method and characterized by transmission electron microscopy and X-ray diffraction techniques. The synthesized Fe@MgAl-LDHs nanoparticles were investigated for magnetic solid phase extraction (MSPE) of 1-naphthol and 2-naphthol from the water samples. The elutent containing 1-naphthol and 2-naphthol was analyzed by high performance liquid chromatography with variable wavelength detection (HPLC–UV). Under optimal conditions, there is good linear relationship between the concentration and the peak area in the range of 0.5–200 μg L −1 with the correlation coefficients ( r 2 ) above 0.998 for 1-naphthol and 2-naphthol. The limits of detection were 0.22 μg L −1 and 0.19 μg L −1 for 1-naphthol and 2-naphthol, respectively, and precisions were both below 2.5% ( n = 6). The real water analysis demonstrated that the spiked recoveries were in the range of 79.2–80.9% ( n = 3). All these results indicated that the developed MSPE–HPLC–UV method was proved to be an efficient tool for the analysis of naphthols.
研究领域:
环境科学
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分析化学
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DOI
高影响因子
ENVIRONMENTAL RESEARCH
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2025
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IF 7.7
Kai Wu,Wenlong Wang,Shubing Yang,Xu Zhang,Peizeng Yang,Yuefei Ji,Jing Chen,Junhe Lu
As global warming intensifies freeze-thaw cycles, the understanding of environmental chemistry processes in ice and their potential impact on global water quality becomes increasingly important. This study investigated the transformation of 1-naphthol in the presence of nitrite (NO 2 - ) under slightly acidic conditions in ice, focusing on the formation of nitro-naphthol. Results demonstrated that increasing NO 2 - concentration enhanced the conversion of 1-naphthol and the formation of nitrated products. This transformation of 1-naphthol was attributed to the freeze-concentration effect, which led to the accumulation of H + , NO 2 - , and 1-naphthol in the liquid-like grain boundary layer amid ice crystals. In this brine, NO 2 - underwent protonation to form reactive nitrous acid (HNO 2 ) and nitrosonium ions (NO + ), which facilitated the nitration, nitrosation, and oxidative coupling reactions, respectively. The pH was shown to influence nitro products formation by altering the HNO 2 to NO + ratio. Toxicity assessment revealed increased toxicity of the NO 2 - /1-naphthol solution after freezing treatment, likely due to the formation of nitrated products, whereas natural organic matter (NOM) reduced this toxicity by suppressing the generation of nitrated products. The findings of this study advance the understanding of NO 2 - chemistry and the behavior of hydroxylated polycyclic aromatic hydrocarbons in cold environments.
研究领域:
环境化学
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物理化学
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化学毒理学
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大气化学
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环境科学
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产品关联
DOI
PubMed
高影响因子
BIOSENSORS & BIOELECTRONICS
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2016
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IF 7.476
Juan Tang,Yapei Huang,Cengceng Zhang,Huiqiong Liu,Dianping Tang
A new impedimetric immunosensor for the fast determination of ochratoxin A (OTA) in food samples was developed based on the instant catalyst as enhancer. Initially, the signal tags were prepared via co-immobilization of anti -OTA antibody and amine-terminated dendrimer (PAMAM) on the graphene oxide nanosheets through the covalent interaction, which were utilized as a good platform for combining manganese ion ( anti -OTA-GO-PAMAM-Mn 2+ ). Upon target OTA introduction, a competitive-type immunoreaction was implemented between the analyte and the immobilized OTA-BSA on the electrode for the anti -OTA antibody on the graphene oxide nanosheets labels. After a competitive immunoassay format, the anti -OTA-GO-PAMAM-Mn 2+ were captured onto the electrode surface , which could induce the in situ formation of MnO 2 via classical redox reaction between Mn 2+ and KMnO 4 on the immunesensing platform. Moreover, the generated MnO 2 nanoparticles act as efficient catalyst could catalyze the 4-chloro-1-naphthol (4-CN) oxidation without H 2 O 2 to generate an insoluble precipitation on the platform. Under the optimal conditions, the instant catalyst based impedimetric immunosensor displayed a wide dynamic working range between 0.1 pg mL −1 and 30 ng mL −1 . The detection limit (LOD) of the assay was 0.055 pg mL −1 . The developed method exhibited high selectivity and can be used for the determination of OTA in real red wine samples.
研究领域:
食品科学
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分析化学
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生物传感器
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
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2021
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IF 10.588
Zi-Jian Chen,Hui-Ling Wu,Yu-Dong Shen,Hong Wang,Yi-Feng Zhang,Bruce Hammock,Zhen-Feng Li,Lin Luo,Hong-Tao Lei,Zhen-Lin Xu
The excessive use of carbaryl has resulted in the risk of its exposure. In this study, we isolated six nanobodies (Nbs) from a camelid phage display library against the biomarker of carbaryl, 1-naphthol (1-NAP). Owing to its characteristics of easy genetic modifications, we produced a nanobody-alkaline phosphatase (Nb-CC4-ALP) fusion protein with good stability. A dual-emission system based ratiometric fluoroimmunoassay (RFIA) for quick and highly sensitive determination of 1-NAP was developed. Silicon nanoparticles (SiNPs) was used as an internal reference and for aggregation-induced emission enhancement (AIEE) of gold nanoclusters (AuNCs), while AuNCs could be quenched by MnO 2 via oxidation . In the presence of ALP, ascorbic acid phosphate (AAP) can be transformed into ascorbic acid (AA), the later can etch MnO 2 to recover the fluorescence of the AuNCs. Based on optimal conditions, the proposed assay showed 220-fold sensitivity improvement in comparison with conventional monoclonal antibody-based ELISA. The recovery test of urine samples and the validation by standard HPLC-FLD demonstrated the proposed assay was an ideal tool for screening 1-NAP and provided technical support for the monitoring of carbaryl exposure.
研究领域:
环境科学
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分析化学
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毒理学
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产品关联
DOI
PubMed
高影响因子
BIOSENSORS & BIOELECTRONICS
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2013
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IF 5.437
Li Hou,Zhuangqiang Gao,Mingdi Xu,Xia Cao,Xiaoping Wu,Guonan Chen,Dianping Tang
A highly sensitive and selective impedimetric immunosensor with triple signal amplification was designed for ultrasensitive detection of prostate-specific antigen (PSA) by using anti-PSA antibody and DNAzyme-functionalized gold–palladium hybrid nanotags (Ab 2 –AuPd–DNA). The signal was amplified based on the Ab 2 –AuPd–DNA toward the catalytic precipitation of 4-choloro-1-naphthol (4-CN). DNAzyme (as a kind of peroxidase mimic) could catalyze the oxidation of 4-CN, whilst AuPd hybrid nanostructures could not only provide a large surface coverage for immobilization of biomolecules but also promote 4-CN oxidation to some extent. The produced insoluble benzo-4-chlorohexadienone via 4-CN was coated on the electrode surface , and hindered the electron transfer between the solution and the electrode, thereby increasing the Faradaic impedance of the base electrode . Three labeling strategies including Ab 2 –AuNP, Ab 2 –AuPd and Ab 2 –AuPd–DNA were investigated for determination of PSA, and improved analytical features were obtained with the Ab 2 –AuPd–DNA strategy. Under optimal conditions, the dynamic concentration range of the impedimetric immunosensor spanned from 1.0 pg mL −1 to 50 ng mL −1 PSA with a detection limit of 0.73 pg mL −1 . Intra- and inter-assay coefficients of variation were below 8.5% and 9.5%, respectively. Importantly, no significant differences at the 0.05 significance level were encountered in the analysis of 6 clinical serum specimens and 6 diluted standards between the impedimetric immunosensor and the commercialized electrochemiluminescent method for PSA detection.
研究领域:
生物传感器
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纳米技术
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分析化学
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癌症诊断
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DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）