JOURNAL OF CHEMICAL AND ENGINEERING DATA
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2018
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IF 2.196
Shuyu Ning,Weifeng Chen,Teng Pan,Youwei Cheng,Lijun Wang,Xi Li
Solubilities of isophthalic acid in ternary mixtures of acetic acid + water + benzoic acid were determined by the static analytical method. The temperature range was from 292.55 to 372.10 K, the mass ratios of water to acetic acid were 0, 1:9, and 1:4, and the mass fractions of benzoic acid in initial solvent ranged from 0 to 20.1%. The experimental results indicated that the solubility of isophthalic acid increased with the introduction of benzoic acid to the binary solvents of acetic acid and water, and that could be explained by Hansen’s three-dimensional parameters and like-dissolves-like rule. Then the experimental solubilities were correlated by the nonrandom two liquids (NRTL) model, and the model parameters were regressed. The values calculated by the NRTL model showed good agreement with the experiment data.
研究领域:
化学工程
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物理化学
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DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
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2023
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IF 8.6
Hongrui Xiang,Feiping Zhao,Tao Wu,Xiaowei Zhang,Fei Chai,Qingwei Wang,Eveliina Repo,Xiaobo Min,Zhang Lin
Understanding the structure–activity relationship between the adsorption performance and accessible adsorption sites plays a vital role in developing efficient adsorbents for Ge(IV) recovery. Herein, three chitosan-based adsorbents were designed by grafting chitosan with p -hydroxybenzoic acid (HBA-CS), 3,4-dihydroxybenzoic acid (DBA-CS), and 3,4,5-trihydroxybenzoic acid (TBA-CS), and the phenolic hydroxyl amounts induced steric effect on Ge(IV) recovery was investigated. The results show that phenolic acids were successfully grafted onto the chitosan surface by an amidation reaction. The adsorption behavior of DBA-CS and TBA-CS conforms to the pseudo-second-order kinetic and Langmuir isotherm models, indicating that it is a single layer adsorption and chemisorption is the main adsorption process . The Ge(IV) recovery performance is correlated with the arrangement of the active adsorption sites and follows the order of TBA-CS > DBA-CS > HBA-CS. The steric effect of TBA-CS is more ideal than that of DBA-CS due to more phenolic hydroxyl groups, which endows it better affinity toward Ge(IV). Additionally, TBA-CS exhibits superior selectivity in the presence of competitive cations and interfering anions, and the adsorption efficiency was not significantly decreased after four regeneration cycles by the acid elution. The chelation adsorption sites for Ge(IV) provided by the o -phenolic hydroxyl groups are the dominant contribution, and the hydrogen bond and ideal steric effect further enhance the adsorption performance of TBA-CS. The structure regulation designed by steric hindrance optimization strategy to achieve high affinity is an attractive approach, which could be extended in the recovery of precious metal ions.
研究领域:
环境科学
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材料科学
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化学工程
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DOI
高影响因子
STAR Protocols
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2024
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IF 1.3
Xinze Du,Yumei Liu,Xiaojun Shen
Summary Phenolic chemicals are important building blocks in chemical and material industries. In this protocol, we describe the preparation of CeO 2 -CuO catalysts and the application in the decarboxylative oxidation reaction of benzoic acids to phenols. Furthermore, we describe how to modify the basic sites of CeO 2 -CuO catalysts by CO 2 treatment to increase the selectivity of phenol and the regeneration process of used catalyst. For complete details on the use and execution of this protocol, please refer to Du et al. (2023). 1
研究领域:
催化
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有机化学
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材料科学
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DOI
PubMed
高影响因子
CERAMICS INTERNATIONAL
·
2024
·
IF 5.1
Hao Wu,Pinquan Qin,Shaowen Cao,Guoqiang Luo,Chuanbin Wang,Rong Tu,Qiang Shen,Lianmeng Zhang
The ability to control the particle size of titanium dioxide nanoparticles (TNPs) is crucial for their practical use. This study presents a method for preparing monodisperse amorphous and anatase TNPs with high surface areas and tunable grain sizes. The method combines a sol-gel process with a hydrothermal process, using benzoic acid (BA) as a structure-directing agent. By adjusting the hydrolysis and condensation rates of the titanium alkoxide, we can synthesize monodisperse amorphous TNPs with a controllable size range of 200–800 nm. Additionally, the amorphous TNPs synthesized through this method serve as raw material, enabling the morphology of anatase TNPs to be inherited from amorphous TNPs with a hydrothermal reaction time of 1 h. When the hydrothermal reaction time is extended to 10 h, the closely linked primary titanium dioxide is fully separated and replaced by ultra-fine anatase TNPs. This optimal scheme show promise for self-assembly and large-scale synthesis of monodisperse amorphous and anatase TNPs.
研究领域:
材料科学
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纳米技术
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DOI
高影响因子
Journal of Environmental Sciences
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2017
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IF 2.865
Huan Li,Lan Cao,Changjun Yang,Zhehui Zhang,Bingguang Zhang,Kejian Deng
A novel magnetically recoverable thioporphyrazine catalyst (CoPz(S-Bu) 8 /SiO 2 @Fe 3 O 4 ) was prepared by immobilization of the cobalt octkis(butylthio) porphyrazine complex (CoPz(S-Bu) 8 ) on silica-coated magnetic nanospheres (SiO 2 @Fe 3 O 4 ). The composite CoPz(S-Bu) 8 /SiO 2 @Fe 3 O 4 appeared to be an active catalyst in the oxidation of benzyl alcohol in aqueous solution using hydrogen peroxide (H 2 O 2 ) as oxidant under Xe-lamp irradiation, with 36.4% conversion of benzyl alcohol, about 99% selectivity for benzoic acid and turnover number (TON) of 61.7 at ambient temperature. The biomimetic catalyst CoPz(S-Bu) 8 was supported on the magnetic carrier SiO 2 @Fe 3 O 4 so as to suspend it in aqueous solution to react with substrates, utilizing its lipophilicity. Meanwhile the CoPz(S-Bu) 8 can use its unique advantages to control the selectivity of photocatalytic oxidation without the substrate being subjected to deep oxidation. The influence of various reaction parameters on the conversion rate of benzyl alcohol and selectivity of benzoic acid was investigated in detail. Moreover, photocatalytic oxidation of substituted benzyl alcohols was obtained with high conversion and excellent selectivity, specifically conversion close to 70%, selectivity close to 100% and TON of 113.6 for para-position electron-donating groups. The selectivity and eco-friendliness of the biomimetic photocatalyst give it great potential for practical applications.
研究领域:
化学
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环境科学
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材料科学
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产品关联
DOI
PubMed
高影响因子
FOOD CHEMISTRY
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2025
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IF 9.8
Caiyun Liu,Fujing Zheng,Huiying Li,Mario Prejanò,Guojie Jin,Yongsheng Tao,Yunkui Li
This study investigated molecular interactions between benzoic acids (gallic acid/protocatechuic acid) and acetate esters using thermodynamics and quantum mechanics, as well as the effects of benzoic acids on acetate esters release and perception in simplified and real wine systems, respectively. Results showed spontaneous binding (ΔG < 0) between benzoic acids and acetate esters (ethyl octanoate > ethyl hexanoate > isoamyl acetate > ethyl butyrate > ethyl acetate), with gallic acid exhibiting stronger affinities. The OH of benzoic acids and COO of acetate esters were the key groups, driven synergistically by hydrogen bonding, dispersion interactions, and hydrophobic effects, while electrostatic contributions dominated interaction energies (43–60 %). Benzoic acids significantly reduced acetate esters release, showing structure- and concentration-dependent trends. Aroma profile and perception revealed benzoic acids promoted formation and retention of fermentation aroma, enhancing flavor and fruitiness. These findings provided mechanistic insights for modulating wine aroma through benzoic acid- acetate ester interactions.
研究领域:
食品科学
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化学
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DOI
PubMed
高影响因子
CRYSTENGCOMM
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2020
·Vol. 22
·期 34
·5628-5637
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IF 3.117
Jinyue Yang,Na Wang,Beiqian Tian,Xiongtao Ji,Baohong Hou,Ting Wang,Xin Huang,Junquan Su,Zhanao Yang,Hongxun Hao
To investigate the effect of positional isomerism on cocrystallization and reveal the role of weak interactions in the formation of cocrystals, experimental characterization complemented with theoretical computations was thoroughly conducted by using p-hydroxybenzoic acid (PHBA), o-hydroxybenzoic acid (OHBA), m-hydroxybenzoic acid (MHBA) and malonic acid (MA) as model compounds. Selective formation of a new cocrystal was discovered between PHBA and MA molecules via several methods, while no cocrystal was formed between OHBA/MHBA and MA molecules. The PHBA–MA cocrystal was thoroughly characterized and analyzed through several solid characterization techniques such as powder X-ray diffraction (PXRD), differential scanning calorimetry (DSC) analysis, Fourier transform infrared (FTIR) spectroscopy, single crystal X-ray diffraction (SCXRD), etc. Taking advantage of a myriad of computational modelling techniques, the molecular recognition mechanism which drove the formation of cocrystals was comprehensively investigated and understood at a molecular level. The structural change accompanied by the cocrystal formation could be rationalized by FTIR spectroscopy and electron density variation analysis. Hirshfeld surface (HS) analysis indicated that O–H⋯O hydrogen bonds played a critical role in the formation of this cocrystal. Molecular electrostatic potential (MESP) surface analysis was employed to predict the interaction sites for cocrystallization, which were in good accordance with the experimental results. Moreover, possible reasons for the selective cocrystallization were analyzed and proposed.
研究领域:
化学
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材料科学
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晶体学
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DOI
高影响因子
ANALYTICAL CHEMISTRY
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2020
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IF 6.785
Bo Wang,Shuai Zheng,Yan Huang,Ying Wang,Zhenyu Zhu,Ran Ma,Yu Zhao,Xijie Yin,Jing Su,Juan Xiong,Benli Zhang,Youping Zhou
The 18O/16O (and 15N/14N) ratio of natural nitrate (NO3–) and nitrite (NO2–) can be used to extract valuable information about their source and fate as environmental contaminants, their metabolism as macronutrients in plants and animals, and their behavior in the N biogeochemical cycle. We developed an accurate, precise, sensitive (minimum sample size: 0.2 μg NO3–-equivalent), and reliable (minimal oxygen exchange, loss, or gain) method to selectively isolate and purify nitrate and nitrite from natural water, soil, air, and plant materials by strong anion exchange (SAX) for low- to normal-salinity samples or strong cation exchange (SCX) for high-salinity samples, followed by quantitative conversion to their respective benzyl esters, which can be separated and individually analyzed for δ18O (and potentially δ15N) by gas chromatography (GC)/pyrolysis/GC/isotope-ratio mass spectrometry (IRMS). The method compares favorably with the currently popular bacterial denitrification and chemical reduction methods, in terms of sensitivity and reliability, and has the potential to simultaneously measure δ15N and δ18O of nitrate and nitrite from natural samples of various origins.
研究领域:
环境科学
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生物地球化学
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DOI
PubMed
高影响因子
DALTON TRANSACTIONS
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2018
·Vol. 48
·期 3
·989-996
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IF 4.099
Ling Yang,Tian Zhao,Ishtvan Boldog,Christoph Janiak,Xiao-Yu Yang,Qiang Li,Yan-Jia Zhou,Yong Xia,Deng-Wang Lai,Yue-Jun Liu
The concentration of benzoic acid was found to exercise efficient control over the formation of either MIL-101(Cr) or MIL-88B(Cr) under otherwise similar hydrothermal synthetic conditions. Nanocrystals of MIL-101(Cr) with ∼100 nm average size and excellent SBET = 3467 m2 g−1 are obtained at lower concentrations of benzoic acid, while at higher concentrations the microparticulated MIL-88B(Cr) product is formed. Hereby a new efficient synthetic method towards the elusive MIL-88B(Cr), yet reported only once without synthetic details, is proposed. The obtained MIL-88B(Cr) has an interesting and potentially valuable property of retaining its high-volume form (Vcell ∼ 2000 Å3) after thermal activation. The degassing of MIL-88B(Cr) in a vacuum at 250 °C yields a porous material with a SBET area of 1136 m2 g−1, which is around the theoretical maximum. The transition to the denser ‘closed’ form (Vcell ∼ 1500 Å3) occurs only at 350 °C, when all of the benzoate/benzoic acid, hindering the process, is removed.
研究领域:
材料科学
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化学工程
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产品关联
DOI
PubMed
高影响因子
ORGANIC & BIOMOLECULAR CHEMISTRY
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2019
·Vol. 17
·期 15
·3760-3764
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IF 3.49
Qinghua Zhu,Yongxiang Song,Hongbo Huang,Qinglian Li,Jianhua Ju
The antimicrobial nucleoside antibiotic A201A is produced by the deep-sea derived Marinactinospora thermotolerans SCSIO 00652. Bioinformatics analysis revealed that mtdV, downstream within the A201A biosynthetic gene cluster, encodes a protein with low homology to a group of chorismate pyruvate-lyases. To explore the role of mtdV in A201A biosynthesis, mtdV was inactivated and HPLC analysis revealed that the resulting ΔmtdV mutant failed to produce A201A; production was partially restored by adding exogenous 4-hydroxybenzoic acid (4HB) to the fermentation. In vitro biochemical assays showed that MtdV catalyzes the conversion of chorismate into 4HB, thereby firmly demonstrating that MtdV is a chorismate lyase involved in A201A biosynthesis. In addition, supplementation of the ΔmtdV mutant with various 4HB analogs enabled production of seven new A201A analogs. Antimicrobial assays showed that the purified A201A analogs 3′-F-A201A and 3′-Cl-A201A were just as active as A201A against the test strains with MIC values of 1–8 μg mL−1.
研究领域:
微生物学
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生物化学
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药学
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DOI
PubMed
高影响因子
Coatings
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2022
·Vol. 12
·期 11
·1729
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IF 3.236
Cong-Cong Luan,Yu-Ping Zhang,Cheng-Xing Cui,De-Liang Chen,Yuan Chen,Meng-Jun Chen
In this paper, a novel pH-responsive brass mesh modified by 3-mercaptobenzoic acid (MBA) and 2-naphthalenethiol (NPT) was demonstrated via a facile chemical etching method followed by surface modification. The smart wettability was dependent on the assembled MBA and NPT with suitable thiol proportions. The on–off control of water penetrating intelligently into the nanostructured brass mesh substrate was carried out by the pH change in the outside environment. The brass mesh modified with XNPT= 0.4 (mole fraction of NBT in the mixed solution) exhibited the strongest pH responsivity from superhydrophobicity to superhydrophilicity. Furthermore, the resulted Janus membrane (JM) fabricated by the integration of a smart brass mesh and hydrophobic Ni foam could be used as a water diode in air and liquid systems. Unidirectional penetration for the water droplet was realized by the resulting smart JM with a hydrophobic upper layer and a pH-responsive layer below.Keywords:smart material;brass mesh;3-mercaptobenzoic acid;2-naphthalenethiol;Janus membrane
研究领域:
材料科学
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化学工程
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产品关联
DOI
高影响因子
DYES AND PIGMENTS
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2024
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IF 4.1
Xiaochen Zhu,Haiyan Qi,Tao Jing,Jun Li,Ming Zhao,Jiayu Zhang,Chao Luo,Maoxia Ran
4-Hydroxybenzoic acid is one of the important metabolism biochemical markers of the urine in gastric cancer patients. In this work, a fluorescence sensor based on N,S-doped carbon dots conjugated molecular imprinting polymers (N,S-CDs@SiO 2 @MIPs) was prepared to detect4-hydroxybenzoic acid. The novel fluorescence sensor in response to 4-hydroxybenzoic acid ranged from 0 to 100 μmol/L, with a detection limit of 1.27 μmol/L. Furthermore, 4-hydroxybenzoic acid demonstrated strong fluorescence quenching capability on our fluorescence sensor, with the fluorescence quenching mechanism involving a combined effects of dynamic quenching and electron transfer. Lastly, the N,S-CDs@SiO 2 @MIPs were applied to analyze 4-hydroxybenzoic acid inhuman urine samples with high accuracy. The findings showed that N,S-CDs@SiO 2 @MIPs sensor might have high potential for effectively, selectively, accurately diagnosing gastric cancer patients.
研究领域:
分析化学
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医学诊断
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材料科学
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产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）