MICROCHIMICA ACTA
·
2011
·Vol. 175
·期 3
·341-346
·
IF 2.578
Jiang Xinyu,Zhang Hui,Chen Xiaoqing
We report on the determination of bisphenol A and 2-naphthol in water samples using ionic liquid cold-induced aggregation dispersive liquid-liquid microextraction combined with HPLC. Parameters governing the extraction efficiency (disperser solvent, volume of extraction and disperser solvent, pH, temperature, extraction time) were optimized and resulted in enrichment factors of 112 for bisphenol A and of 186 for 2-naphthol. The calibration curve was linear with correlation coefficients of 0.9995 and 0.9998, respectively, in the concentration range from 1.5 to 200 ng mL −1 . The relative standard deviations are 2.3% and 4.1% (for n = 5), the limits of detection are 0.58 and 0.86 ng mL −1 , and relative recoveries in tap, lake and river water samples range between 100.1 and 108.1%, 99.4 and 106.2%, and 97.1 and 103.8%, respectively.
IL-CIA-DLLME has a high enrichment factor (112, 186), acceptable relative recovery (97.1%–108.1%), good repeatability (2.3%, 4.1%) and a wide linear range(1.5–200 ng mL −1 ) for the determination of bisphenol A and 2-naphthol.
研究领域:
分析化学
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环境科学
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DOI
高影响因子
JOURNAL OF MOLECULAR STRUCTURE
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2022
·
IF 3.841
Mengyu Zhu,Jun Lu,Linchang Dong,Shuheng Hu,Shuchuan Peng,Chengzhu Zhu
The possible photochemical transformation pathways of chlorophenols (2, 6-dichlorophenol and 2-chlorophenol) with superoxide anion radical (O 2 ·− ) were studied by steady-state irradiation and 355 nm laser flash photolysis technique. O 2 ·− was generated by irradiating riboflavin O 2 -saturated solution with an UVA light (maximum at 365 nm). The steady-state experimental results suggested that the transformation efficiency of chlorophenols improved with the increase of the initial riboflavin concentration and solution initial pH value, while the increase of chlorophenols concentration would inhibit the photochemical reaction. The second-order rate constant of the reaction of O 2 ·− with 2, 6-DCP phenoxyl radical (2, 6-DCP · ) and 2-CP phenoxyl radical (2-CP · ) were determined as (8.39 ± 0.99) × 10 9 L mol −1 s −1 and (5.17 ± 0.68) × 10 9 L mol −1 s −1 by laser flash photolysis techniques, respectively. The transformation of chlorophenols was accompanied by the formation of Cl − induced by superoxide radicals after the mixed riboflavin and chlorophenols solution with UVA irradiation. The main conversion products of the reaction between 2, 6-DCP and O 2 ·− were identified by GC-MS, as 2-chlorophenol, 2, 6-dichloro-1, 4-benzoquinone, 2, 6-dichloro-hydroquinone and 3-chlorocatechol, while 2-CP with O 2 ·− was 2-chloro-1, 4-benzoquinone, 2-chlorohydroquinone and phenol, respectively. The transformation pathways of 2, 6-DCP and 2-CP with O 2 ·− were also proposed.
研究领域:
环境科学
·
化学
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DOI
高影响因子
FOOD CHEMISTRY
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2021
·
IF 7.514
Yun Zhao,Yun-Hai Yang,Min Ye,Kai-Bo Wang,Li-Ming Fan,Fa-Wu Su
In this study, the chemical composition of the essential oil (EO) of Origanum vulgare was characterized, and the antifungal activity of the EO and some individual components against Botrytis cinerea (Y-BC-1) was determined . Twenty-one components were identified by gas chromatography–mass spectrometry and gas chromatography–flame ionization detection, constituting 95.7% of the EO. The major components were methyleugenol (16.5%), myristicin (15.6%), carvacrol (15.0%), thymol (9.8%), apioline (9.4%), and (Z)-β-farnesene (8.7%). B. cinerea in vitro mycelial growth and spore germination were strongly inhibited by the EO and two of its main components, thymol and carvacrol. In vivo vapor contact assays, the antifungal activity of the EO at 250 mg/L suppressed the decay of cherry tomatoes 96.39%. Moreover, thymol and carvacrol at 125 mg/L completely suppressed the gray mold. Thus, the EO of O. vulgare is a potentially nontoxic and ecofriendly botanical fungicide for postharvest control of gray mold.
研究领域:
植物学
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真菌学
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食品科学
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DOI
高影响因子
Chemistry-Switzerland
·
2024
·Vol. 6
·期 6
·1622-1634
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IF 2.4
Yumeng Song,Ping Chen,Hui Lou,Xiaoming Zheng,Xiangen Song
This paper studies the catalytic hydrogenation reduction of lignin-derived phenolic compounds, such as catechol, guaiacol (O-methoxyphenol), phenol, P-methylphenol, O-ethylphenol, O-ethoxyphenol, etc. The reaction system focuses on the catalytic performance of hydrodeoxygenation reactions involving the phenolic derivatives of the lignin depolymerization products catechol and guaiacol. A series of Al2O3-TiO2composite oxide supports with different Al/Ti ratios were prepared by a co-precipitation method, and a 5% Pd/Al2O3-TiO2bifunctional catalyst was prepared by an impregnation method and characterized with XRD, SEM, BET, NH3-TPD, etc. Among these, the Pd/Al2Ti1catalyst had the most excellent catalytic performance. At 100 °C and 2 MPa hydrogen pressure, the conversion of catechol was as high as 100%, and at 100 °C and 5 MPa hydrogen pressure, the conversion of guaiacol reached 90%.
研究领域:
催化化学
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生物质转化
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绿色能源
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有机化学
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DOI
高影响因子
ENVIRONMENTAL SCIENCE & TECHNOLOGY
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2013
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IF 5.257
Xubiao Luo,Fang Deng,Lujuan Min,Shenglian Luo,Bin Guo,Guisheng Zeng,Chaktong Au
Inorganic-framework molecularly imprinted TiO2/WO3 nanocomposites with molecular recognitive photocatalytic activity were first prepared successfully by a facile one-step sol-gel method using 2-nitrophenol and 4-nitrophenol as template molecules, and tetrabutyl orthotitanate as titanium source as well as the precursor of functional monomer which could complex with template molecules. The template molecules could be completely removed by means of high-temperature calcination, avoiding the traditional extraction procedures that are time- as well as solvent-consuming. Compared to nonimprinted TiO2/WO3, the molecularly imprinted TiO2/WO3 shows a much higher adsorption capacity and selectivity toward the template molecules. The enhancement in terms of adsorption capacity and selectivity can be attributed to the chemical interaction between target molecules and imprinted cavities, as well as size matching between imprinted cavities and target molecules. The photocatalytic activity of molecularly imprinted TiO2/WO3 toward the target molecules is more than two times that of non-imprinted TiO2/WO3, a result of selective adsorption of target molecules on molecularly imprinted TiO2/WO3. The formation pathway of intermediate products in 2-nitrophenol and 4-nitrophenol degradation process was provided. Moreover, molecularly imprinted TiO2/WO3 exhibits high stability. The results indicate that inorganic-framework molecularly imprinted TiO2/WO3 nanocomposites have a promising prospect in the treatment of wastewater for irrigation.
研究领域:
环境科学
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材料科学
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DOI
高影响因子
CANADIAN JOURNAL OF CHEMICAL ENGINEERING
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2025
·
IF 1.9
Xudong Wang,Yanyang Wu,Tianyou Wang,Bin Wu,Kui Chen,Lijun Ji
M-cresol and p-cresol, typically produced as mixtures in industrial processes, are crucial chemical intermediates. However, their separation is challenging due to their similar structures and properties. ZSM-5 zeolite has shown potential as an adsorbent for separation, while the performance is yet to be improved. In this study, ZSM-5-F(x) was synthesized via hydrothermal method, incorporating F − ions during the synthesis process. The adsorption behaviour of m-cresol and p-cresol on ZSM-5-F(x) was investigated through static experiments, with ZSM-5-F(8) demonstrating the highest selectivity (9.01). Both ZSM-5-F(0) and ZSM-5-F(8) were characterized using XRD, scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) techniques. In addition, the introduction of F − ions increased the material's electronegativity, as demonstrated by the change in zeta potential from 53.22 to −45.93 mV. Single-component adsorption of m-cresol or p-cresol on ZSM-5-F(0) and ZSM-5-F(8) respectively were investigated in detail. The adsorption of m-cresol on ZSM-5-F(8) showed a non-monotonic phenomenon with a significant decrease after 0.06 mol/L. The thermodynamic parameters including Δ G , Δ H , and Δ S were calculated accordingly. All the values |Δ G |, |Δ H |, and |Δ S | of both components on ZSM-5-F(8) were greater than those on ZSM-5-F(0), suggesting that the introduction of F − ions facilitated the adsorption. Competitive adsorption experiments on both ZSM-5-F(0) and ZSM-5-F(8) were conducted at 298.2 K. The results indicated that the selectivity α p/m on ZSM-5-F(8) increased with increasing initial concentration and laid between 13 and 14. After seven consecutive regeneration cycles, the selectivity (α p/m ) only decreased to 13. This study suggests that ZSM-5-F(8) could be a promising adsorbent for m-cresol and p-cresol in industrial applications.
研究领域:
化学工程
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材料科学
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产品关联
DOI
高影响因子
FOOD RESEARCH INTERNATIONAL
·
2024
·
IF 7
Dong Cai,Xinmiao Wang,Qian Wang,Peiyong Tong,Weiyuan Niu,Xu Guo,Jinghan Yu,Xuan Chen,Xiaoyang Liu,Dayong Zhou,Fawen Yin
The β-cyclodextrin and short-chain alkyl gallates (A-GAs), which are representative of phenolipids, such as butyl, propyl, ethyl, and methyl gallates, were chosen to form inclusion complexes by the use of the freeze-drying process. In the everted rat gut sac model, HPLC-UV analysis demonstrated that the released A-GAs from inclusion complexes were degraded to yield free gallic acid (GA) (sustained-release function 1). The small intestine membrane may be crossed by both the GA and the A-GAs. A-GAs may also undergo hydrolysis to provide GA (sustained-release function 2) following transmembrane transfer. Clearly, a helpful technique for the dual sustained-release of phenolic compounds is to produce β-cyclodextrin inclusion complexes with short-chain phenolipids. This will increase the bioactivities of phenolic compounds and prolong their in vivo residence length. Moreover, changing the carbon-chain length of these β-cyclodextrin inclusion complexes would readily modify the dual sustained-release behavior of the phenolic compounds. Thus, our work effectively established a theoretical foundation for the use of β-cyclodextrin inclusion complexes containing short-chain phenolipids as new source of functional food components to provide the body with phenolic compounds more efficiently.
研究领域:
食品科学
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药理学
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生物化学
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE
·
2024
·
IF 3.3
Wenyu Cui,Fuchun Chen,Zhaoyue Sun,Caifang Cui,Ben Xu,Weijun Shen,Fachun Wan,Anwei Cheng
BACKGROUND Grape peels, the main by-products of wine processing, are rich in bioactive ingredients of phenolics, including proanthocyanidins, flavonoids and anthocyanins. Phenolics have the function of regulating intestinal microbiota and promoting intestinal health. From the perspective of the dietary nutrition of grape peel phenolics (GPP), the present study aimed to investigate the influence of GPP on the composition and metabolism of human gut microbiota during in vitro fermentation. RESULTS The results indicated that GPP could decrease pH and promote the production of short-chain fatty acids. ACE and Chao1 indices in GPP group were lower than that of the Blank group. GPP enhanced the levels of Lachnospiraceae UCG-004 , Bacteroidetes and Roseburia , but reduced the Firmicutes / Bacteroidetes ratio. Kyoto Encyclopedia of Proteins and Genome enrichment pathways related to phenolic acid metabolism mainly included flavonoid, anthocyanin, flavone and flavonol biosynthesis. Gut microbiota could accelerate the release and breakdown of phenolic compounds, resulting in a decrease in the content of hesperetin-7- O -glucoside, delphinidin-3- O -glucoside and cyanidin-3-rutinoside etc. In vitro antibacterial test found that GPP increased the diameters of the inhibition zones of Escherichia coli and Staphylococcus aureus in a dose-dependent manner. CONCLUSION The results of the present study revealed that GPP might be a potential prebiotic-like to prevent diseases by improving gut health. The findings could provide a theoretical basis for the potential to exploit GPP as dietary nutrition to maintain intestinal function. © 2024 Society of Chemical Industry.
研究领域:
食品科学
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微生物学
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营养学
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产品关联
DOI
PubMed
高影响因子
FOOD CHEMISTRY
·
2024
·
IF 8.5
Ning Li,Chenxi Ren,Qin Hu,Bo Wang,Zhenquan Yang,Lixia Xiao,Tianzhu Guan
Intake of 17β-estradiol (E2), bisphenol A (BPA), and diethylstilbestrol (DES) from food can contribute to endocrine disorders. Therefore, developing a sensitive method for the simultaneous detection of E2, BPA, and DES and understanding their combined effects on endocrine disruption are crucial. We developed a fluorescence aptasensing platform utilizing DNase I–assisted cyclic enzymatic signal amplification in conjunction with an aptamer/graphene oxide complex. Using PEG 20000 as a surface-blocking agent, the aptasensor achieved ultralow detection limits of 2.643, 0.3039, and 0.6996 for E2, BPA, and DES, respectively. The sensor demonstrated accurate detection in plastic bottled water at spiked levels of 10 and 100 ng/mL. Systems toxicology revealed 30 potential targets for mixture-induced endocrine disruption. Molecular docking showed binding affinities of E2, BPA, and DES for ESR1 of −9.94, −8.29, and − 8.98 kcal/mol, respectively. These results highlight the effectiveness of the aptasensor and provide valuable insights into endocrine disruption mechanisms.
研究领域:
分析化学
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毒理学
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环境科学
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产品关联
DOI
PubMed
高影响因子
APPLIED SURFACE SCIENCE
·
2016
·
IF 3.15
Jin Feng,Qiang Wang,Dongliang Fan,Lirong Ma,Deli Jiang,Jimin Xie,Jianjun Zhu
In order to investigate the roles of three-dimensional network structure and calcium on Ni catalysts, the Ni, Ni-Al 2 O 3 , Ni-Ca-Al 2 O 3 xerogel catalysts were successfully synthesized via the fast sol-gel process and chemical reduction method. The crystal structure of three different catalysts was observed with X-ray powder diffraction (XRD). Transmission electron microscopy (TEM), scanning electron microscopy (SEM) and nitrogen adsorption-desorption were employed to investigate the role of network structure of xerogel catalysts and the size distribution of Ni nanoparticles. The catalyst composition was determined by inductively coupled plasma-optical emission spectrometry (ICP-OES) measurement and energy-dispersive X-ray spectroscopy (EDS). Temperature-programmed reduction (TPR) experiments were carried out to investigate the reducibility of nickel species and the interaction between nickel species and alumina. The catalytic hydrogenation of p -nitrophenol to p -aminophenol was investigated over the prepared nickel-based xerogel catalysts. The conversion of p -nitrophenol was monitored by UV spectrophotometry and high performance liquid chromatography (HPLC). The results show that the catalysts are highly selective for the conversion of p -nitrophenol to p -aminophenol and the order of catalytic activities of the catalysts is Ni < Ni-Al 2 O 3 < Ni-Ca-Al 2 O 3 . The catalysts were recycled and were used to evaluate the reutilization.
研究领域:
化学工程
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催化科学
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DOI
高影响因子
CATALYSIS LETTERS
·
2024
·Vol. 154
·期 8
·4756-4767
·
IF 2.3
Liu Kande,Wang Sitan,Zheng Lishan,Lou Shifeng,Meng Xuan,Cao Fahai,Liu Naiwang,Shi Li
The catalytic performance of Hβ zeolite treated with different concentration of NaOH on the alkylation of tert-butanol with phenol was studied. The effect of NaOH concentration on the crystallinity, morphology, textural property and acidity of Hβ zeolite was studied by X-ray diffraction (XRD), scanning electron microscope characterization (SEM), N 2 adsorption–desorption, Fourier transform infrared spectroscopy (FT-IR) and pyridine adsorption infrared spectra (Py-IR) techniques. A certain concentration of NaOH treatment can regulate the pore structure of Hβ zeolite and remove part of framework aluminum and framework silicon, thus achieving the purpose of regulating the pore structure and acidity of the catalyst. Though lower Bronsted to Lewis acid amount ratio when treated NaOH concentrations were 0.15 mol/L, leading to the increasing of selectivity to 4-TBP. The Hβ-0.2 M showed the high selectivity of 90.21% for synthesis of 4-tert-butyl-phenol (4-TBP), compared with the unmodified parent zeolite, the selectivity of 4-TBP improved 16.7%. Graphical Abstract
研究领域:
催化化学
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材料科学
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DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2021
·
IF 4.464
Xianyu Kang,Yingying Song,Jingchuang Zhao,Yancai Li
In this work, three-dimensional interconnected porous carbon (3DIPC) materials were successfully prepared by a simple one-step pyrolysis reaction from sodium citrate. Then, the 3DIPC was combined with 1-vinyl-3-ethylimidazolium tertrafluoroborate [(VEIM)BF 4 ] and ultrasonicated to form 3DIPC-ionic liquid (3DIPC-IL). Transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), X-ray diffraction (XRD), and atomic force microscopy (AFM) were used to determine the structure and morphology of the 3DIPC and 3DIPC-IL. The fabricated 3DIPC-IL chitosan coated glassy carbon modified electrode (3DIPC-IL/CS/GCE) displayed good electrocatalytic activity toward paracetamol (PA), dopamine (DA), and bisphenol A (BPA). Using this technique, PA and DA can be detected simultaneously and BPA can be detected as well. Under ideal conditions, the sensor displays two linear ranges of 1.0 to 200 μM and 200 to 700 μM for PA and of 1.0 to 100 μM and 100 to 500 μM for DA. In addition, a linear range of 2.0 to 100.0 μM was established for BPA. The detection limits of PA, DA, and BPA were determined to be 0.58 μM, 0.13 μM, and 0.028 μM (S/N = 3), respectively. The 3DIPC-IL/CS/GCE also exhibits high sensitivity, good stability, and good selectivity for the determination of PA, DA, and BPA.
研究领域:
分析化学
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材料科学
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环境科学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）