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CHINESE JOURNAL OF CHEMISTRY · 2011 ·Vol. 29 ·期 4 ·778-782 · IF 0.773

Determination of Glycolate Acid, Mono- and Dichloroacetic Acids in Synthetical Betaine by Anion-exchange Chromatography

Haining Shi,Zonghua Wang,Hui Wang,Rui Zhao,Mingyu Ding

An anion-exchange chromatography method combined solid phase extraction (SPE) was developed for the simultaneous analysis of glycolate acid (GL), monochloroacetic acid (MCA) and dichloroacetic acid (DCA) in synthetical betaine products. The analytes and unknown anionic impurities were well separated on a Metrosep A supp5 anion-exchange column (150 mm×4 mm) with 2.0 mmol/L Na 2 CO 3 +2.0 mmol/L NaHCO 3 solution as eluent. Suppressed conductivity detection was used. A strong cation exchange (SCX) solid phase extraction (SPE) cartridge was used to reduce the concentration of matrix betaine and a Cleanert IC-Ag pretreatment cartridge was used to remove high Cl − concentration. The detection limits of GL, MCA and DCA were 0.09, 0.017 and 0.05 µg/L, respectively. The relative standard deviations (RSDs) of the retention times and peak areas were less than 0.09% and 0.49%, respectively. The recoveries of the three analytes were between 90.6% and 100.8%. The analytical results showed that GL and DCA were present in high concentration and no MCA was found when the proposed ion chromatography method was applied to three synthetical betaine samples. The proposed method is simple, sensitive and timesaving, and is also suitable for routine analysis in quality control of synthetical betaine products.

研究领域: 分析化学 · 药物质量控制 · 分离科学 · 环境分析 · 食品化学
✓ 已验证 DOI 高影响因子
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FLUID PHASE EQUILIBRIA · 2010 ·Vol. 293 ·期 1 ·73-78 · IF 1.857

Liquid–liquid equilibrium of the ternary system water + acetic acid + sec-butyl acetate

Song Hu,Qing-lin Chen,Bing-jian Zhang,Yuan-lan Liang,Xue-nong Gao

Experimental liquid–liquid equilibrium (LLE) of the water–acetic acid–sec-butyl acetate ternary system was investigated at 298.15, 303.15, 308.15 and 313.15   K and at atmospheric pressure. Separation factors were also evaluated for the immiscibility region. The NRTL and UNIQUAC models were applied to fit the experimental data for the ternary system . The binary interaction parameters obtained from both models were found to be successfully correlated with the equilibrium compositions . The UNIFAC group contribution method was employed to predict the observed ternary LLE data. It was found that four types of the UNIFAC model (UNIFAC, UNIFAC-LL, UNIFAC-DMD, and UNIFAC-LBY) did not provide a good prediction of the LLE data for this ternary system .

研究领域: 化学工程 · 热力学 · 分离科学 · 过程工程
✓ 已验证 DOI 高影响因子
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ADVANCED ENGINEERING MATERIALS · 2020 ·Vol. 22 ·期 11 ·2000519 · IF 3.217

Customizing the Pore Structure and Properties of Freeze-Cast Porous Titanium by Zirconium Acetate Additive

Chuan Zong Wu,Zhu Yin Chen,Xinli Liu,Ting Shen,LiGuo Zu,Lei Zhang

Porous titanium scaffolds with high porosity and connected macropores are fabricated by adding zirconium acetate to control the ice crystal growth during freeze casting. The influences of zirconium acetate additives on the phase composition, pore structure, and mechanical properties of porous titanium are studied. As modified by zirconium acetate, the X-ray diffraction peaks of titanium moves to a smaller angle, and the zirconium is evenly distributed on the titanium matrix. With the increase in the concentration of zirconium from 0 to 60 g L −1 , the pore morphology of porous titanium changes from typical lamellar to the honeycomb, the pore size distribution becomes wider. The average pore size and porosity increases from 44 ± 11 to 126 ± 35 μm and from 46.4 ± 1.3 to 59.1 ± 1.3%, respectively. As the concentration of zirconium acetate is 40 g L −1 , the porosity and the pore size of the porous titanium scaffolds are comparable with those modified by 10 g L −1 zirconium acetate, but the compressive strength is 2.3 times higher. Zirconium acetate as an additive has an excellent performance in optimizing the pore structure and mechanical properties of water-based freeze-cast porous titanium.

研究领域: 生物材料学 · 组织工程 · 金属材料科学 · 医用植入材料 · 多孔材料
✓ 已验证 DOI 高影响因子
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Journal of Energy Storage · 2024 · IF 8.9

A novel “point-to-point” 1,4-phenylenediacetic acid grafting of Ti3CN enhances sodium storage stability

Hao Chen,Si-Miao Huang,Dong-Ting Zhang,Min-Peng Li,Chen-Yang Li,Yu-Ping Qiu,Xiao-Rui Wang,Tian-Peng Xu,Mao-Cheng Liu

The self-stacking of MXenes-Ti 3 CN limits the accessibility of nanochannels , reduces the ion diffusion kinetics, and hinders its application in alkali metal ion storage field. This study proposes a point-to-point mortise and tenon joining strategy to fabricate a composite structure of 1,4-phenylenediacetic acid-Ti 3 CN (1,4-PDEA-Ti 3 CN) by grafting rigid and flexible 1,4-phenylenediacetic acid (1,4-PDEA) into the amino-functionalized Ti 3 CN interlayers. The rigid and flexible 1,4-PDEA contributes to a pillar effect in the layered structure of Ti 3 CN, which is benefit to prevent the self-stacking and maintain a stable 2D layered structure. As a result, the interlayer spacing of Ti 3 CN is expanded from 1.20 to 1.46 nm and the Na + diffusion coefficient is improved from 1.16 × 10 −6 to 1.99 × 10 −6  cm 2  s −1 after point-to-point 1,4-PDEA grafting. The 1,4-PDEA-Ti 3 CN achieves a reversible discharge specific capacity of 202.3 mAh g −1 at a current density of 0.1 A g −1 after 770 cycles. Even at a high current density of 5 A g −1 , the 1,4-PDEA-Ti 3 CN still possesses a reversible discharge specific capacity of 137 mAh g −1 and it still maintains the high specific capacity of 256.1 mAh g −1 when the current density comes back to 0.1 A g −1 . This point-to-point mortise and tenon joining strategy provides a novel approach for designing other 2D energy storage materials with long cycle stability and high-rate capability.

研究领域: 材料科学 · 电化学储能 · 纳米材料 · 能源化学 · 二维材料
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF FOOD PROPERTIES · 2019 · IF 1.398

Foaming, emulsifying properties and surface hydrophobicity of soy proteins isolate as affected by peracetic acid oxidation

Junsheng Li,Bixuan Wang,Junfu Fan,Xin Zhong,Guoxia Huang,Liujuan Yan,Xiane Ren

In this study, the effects of the disulfide bond cleavage induced by peracetic acid oxidation on the surface properties and surface hydrophobicity of soy proteins isolate (SPI) were investigated. The surface hydrophobicity, foaming capacity and emulsifying capacity of oxidized-SPI increased gradually at the initial stage with the increase of peracetic acid concentration. When the concentration of peracetic acid was increased up to 0.4%, compared with that of native SPI, the surface hydrophobicity, foaming capacity, emulsifying capacity and emulsifying stability of oxidized-SPI increased by 114.0, 81.4, 65.2, 49.8%, respectively, and achieved optimal results. However, excessive oxidation led to a decrease in surface hydrophobicity, foaming capacity and emulsifying stability of SPI, but it had no obvious effect on the foaming stability and emulsifying capacity of SPI. The foaming capacity, emulsifying capacity and emulsifying stability of SPI were positively related to the changes of surface hydrophobicity which caused by disulfide bond cleavage. The results of fluorescence spectroscopy, CD spectroscopy, and particle size analysis showed that the disulfide bond cleavage did cause great changes in the molecular structure of SPI, but there was no clear correlation between the molecular structural change and the surface activity of SPI. These suggested that the improvement of foaming capacity, emulsifying capacity and emulsifying stability of SPI could be achieved by changing its surface hydrophobicity via peracetic acid oxidation.

CAS / MDL: 70-18-8
研究领域: 食品科学 · 生物化学
✓ 已验证 产品关联 DOI 高影响因子
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2019 · IF 4.784

Water addition enhanced thermal stability of alkylimidazolium acetate in Ionosolv treatment of lignin

Junwang Zhang,Lili Song,Kunlan Li,Qingda An,Hao Ma,Liyu Yang,Ligang Wei

Water addition was found to enhance the thermal stability of alkylimidazolium–acetate ionic liquids (ILs). Especially in the case of high water content (30–50 wt%), few decomposition products can be observed in the 1 H NMR spectra even after treatment for 24 h at 150 °C. On the basis of this finding, lignin treatment of water and acetate IL mixtures (50–90 wt% IL content) were investigated at 150 °C. The addition of water, as opposed to pure IL treatment, can inhibit the lignin depolymerization into small fragments. Lignin degradation and the structure of regenerated lignin are more affected by cation types of ILs rather than the IL contents and pH values. In the case of 50–70 wt% 1-ethyl-3-methylimidazolium acetate–water system, the specific inter-unit linkages of lignin can be broken down, and regenerated lignin with a narrow polydispersity index (5.0–9.6) can be obtained.

研究领域: 绿色化学 · 生物质转化 · 高分子化学 · 离子液体化学 · 木质素化学 · 可持续材料 · 热化学转化
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2017 ·Vol. 43 ·期 16 ·14176-14182 · IF 2.986

Polyaceticzirconium for zirconia continuous fibers: Polymeric evolution process and the relationship between polymeric structure and rheological behavior

Lin Wang,Benxue Liu,Luyi Zhu,Yongshuai Xie,Yadong Lv,Chonghe Xu,Xiaotong Jin,Xinqiang Wang,Guanghui Zhang,Dong Xu

Polyaceticzirconium (PEZ) sol, which is the precursor of zirconia (ZrO 2 ) continuous fibers, has been synthesized by means of the reaction between zirconium oxychloride octahydrate (ZrOCl 2 ·8H 2 O) and potassium acetate (CH 3 COOK) in methanol. The polymeric structures and the rheological behaviors of the sols with different molar ratios of ZrOCl 2 ·8H 2 O/CH 3 COOK are different and would affect the spinnability and stability significantly. Herein, the polymeric structures and rheological behaviors of the PEZ sols with the molar ratios of 1:1, 1:1.5, 1:1.8 and 1:2 were investigated by Fourier transform infrared (FT-IR), 1 H nuclear magnetic resonance spectrum ( 1 H-NMR), thermogravimetry and differential thermal analysis (TG/DTA) and rheological measurements. The results showed the carboxyl group acted as a chelating ligand instead of bidentate ligand, and the water molecule coordinated to Zr 4+ was deprotoned gradually with the decrease of the molecular ratios. The different polymeric structures lead to a different rheological behaviors of the sols. It is divided into three types, the Newton fluid with a low viscosity produced by the charged linear polymeric structures, the shear thinning fluid with a high viscosity produced by the three-dimensional polymeric structures and the shear thinning fluids with a proper viscosity produced by the linear twining polymeric structures. Through the experimental guidance, we successfully synthesized a sol with suitable viscosity and stability, and used it to fabricate high quality ZrO 2 fibers.

研究领域: 材料科学 · 无机化学 · 高分子化学 · 纤维工程 · 溶胶-凝胶技术
✓ 已验证 DOI 高影响因子
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RSC Advances · 2018 ·Vol. 8 ·期 66 ·38003-38012 · IF 2.936

Construction of myoglobin–amphiphilic alginate caprylamide–graphene composite modified electrode for the direct electron transfer between redox proteins and electrode and electrocatalysis of myoglobin

Xiuqiong Chen,Huiqiong Yan,Wei Sun,Guangying Chen,Changjiang Yu,Wen Feng,Qiang Lin

To achieve the dispersion of the hydrophobic graphene (GR), the amphiphilic alginate caprylamide (ACA) was synthesized to fabricate electroactive Nafion/Mb–ACA–GR/CILE for the accurate determination of trichloroacetic acid (TCA). SEM observation, FT-IR and UV-Vis spectroscopic analysis indicated that ACA could tightly immobilize Mb and GR on the electrode surface by constructing biointerfaces, which not only provided Mb a suitable microenvironment to maintain its biological activity, but also shortened the distances between the active centers of Mb with carbon ionic liquid electrode (CILE), thus promoting the electron transfer rate. The electrochemical characterization of Nafion/Mb–ACA–GR/CILE showed that the direct electron transfer of Mb was realized on the modified electrode, which was attributed to the high electrical conductivity and excellent electrocatalytic activity of GR and good biocompatibility of ACA. Moreover, Nafion/Mb–ACA–GR/CILE exhibited good electrocatalytic activity towards TCA with the linear range from 2.5 to 47.3 mmol L−1 and lower KMapp value of 8.3 mmol L−1. Moreover, the modified electrode also revealed good stability, reproducibility and accurate detection of tap-water, exhibiting great potential for the applications as the third-generation electrochemical biosensors.

研究领域: 生物医学工程 · 电化学传感 · 纳米生物技术 · 分子生物学 · 分析化学 · 生物传感器
✓ 已验证 DOI 高影响因子
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JOURNAL OF CATALYSIS · 2018 · IF 6.759

Catalytic oxidation of ethyl acetate over Ru–Cu bimetallic catalysts: Further insights into reaction mechanism via in situ FTIR and DFT studies

Xiaolong Liu,Qingzhen Han,Wenbo Shi,Cheng Zhang,Erwei Li,Tingyu Zhu

In this work, ruthenium-based bimetallic catalysts of 1Ru-5 M/TiO 2 (M = Co, Ce, Fe, Mn, Cu, Ni) were prepared and evaluated in ethyl acetate oxidation. It was found that 1Ru-5Cu/TiO 2 gave the highest catalytic activity. The influence of CuO content and the preparation method on the catalytic activity was also studied. 1Ru-5Cu/TiO 2 showed great catalytic stability in the on-stream reaction test. The influence of H 2 O on the catalytic activity is presented. The bimetallic catalyst 1Ru-5Cu/TiO 2 showed better catalytic performance than the monometallic catalysts 1Ru/TiO 2 and 5Cu/TiO 2 . XRD, TEM, HAADF-STEM, H 2 -TPR, and XPS characterizations were conducted, and the synergistic effect between Ru and Cu was well presented. In situ FTIR studies were also conducted, and the reaction intermediates were revealed on the catalyst surface. The theoretical calculations suggested that ethyl acetate is more easily adsorbed on the CuO surface, while it reacts more easily on the RuO 2 surface . Accordingly, a reaction mechanism for the catalytic oxidation of ethyl acetate over a Ru-Cu bimetallic catalyst is proposed.

研究领域: 催化化学 · 环境化学 · 表面科学 · 材料化学 · 物理化学
✓ 已验证 DOI 高影响因子
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Nanoscale · 2018 ·Vol. 11 ·期 3 ·962-967 · IF 7.233

Chemical pre-reduction and electro-reduction guided preparation of a porous graphene bionanocomposite for indole-3-acetic acid detection

Zhaohong Su,Xiaolin Xu,Yongbing Cheng,Yueming Tan,Langtao Xiao,Daili Tang,Hongmei Jiang,Xiaoli Qin,Huixian Wang

A porous graphene (PG) bionanocomposite of PG, gold nanoparticles (AuNPs) and anti-indole-3-acetic acid (anti-IAA) antibody for sensitive and label-free amperometric immunoassay of IAA was reported. A PG film was produced by a pre-reduction/electrochemical reduction process on a glassy carbon electrode (GCE) and then a homogeneous AuNPs layer electrodeposition on the PG film. The anti-IAA antibody was immobilized onto the AuNPs through electrostatic adsorption and covalent conjugation. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy, energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR), cyclic voltammetry (CV), elecro-chemical impedance spectroscopy (EIS), ultraviolet visible spectroscopy (UV-vis) and differential pulse voltammetry (DPV) were used to characterize the PG film and the stepwise modification of the immunosensor. The electrochemical immunosensor exhibited a wide linear range from 2 × 10−11 to 2 × 10−8 g mL−1 with a detection limit of 0.016 ng mL−1 (S/N = 3) and showed significant linearity R2 = 0.9970. In addition, the proposed immunosensor showed acceptable selectivity and has been applied to the determination of IAA in the extract samples of several plant seeds with acceptable relative derivation (%) ranging from −5.25% to 4.24% between the immunosensor and high performance liquid chromatography. The proposed chemical pre-reduction and electro-reduction guided protocol can be extended to the preparation of many other functionalized PG nanocomposite films for wide applications.

研究领域: 生物传感 · 纳米生物技术 · 分析化学 · 植物生理学 · 电化学 · 免疫分析
✓ 已验证 DOI 高影响因子
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NEW JOURNAL OF CHEMISTRY · 2017 ·Vol. 41 ·期 22 ·13319-13326 · IF 3.269

Facile synthesis, crystal structure and bioactivity evaluation of two novel barium complexes based on 2,4,6-trichlorophenoxyacetic acid and o-ferrocenylcarbonyl benzoic acid

Xiuling Xu,Fan Hu,Qi Shuai

Two novel Ba(II) complexes [Ba(TCPA)2(H2O)4] 1 and [Ba(H2O)8]·2(o-FcCOC6H4COO)·6H2O 2 [HTCPA = 2,4,6-trichlorophenoxyacetic acid and o-HOOCC6H4-COFc = o-ferrocenylcarbonyl benzoic acid] have been synthesized by a facile microwave method. The solid-state structures were well established by means of X-ray crystallography as well as routine analysis of the infrared spectrum (FTIR), elemental analysis, field emission scanning electron microscopy (FESEM) and thermogravimetric analysis (TG). Different polyhedra of tricapped triangular prisms for 1 and dodecahedra for 2 were present. It is worth noting that the central Ba(II) ion in 1 is nine-coordinated by two carboxylate oxygen atoms from TCPA ligands and seven oxygen atoms from coordinated water molecules. By contrast, the eight-coordinated Ba(II) in 2 forms barium-water clusters assembled by O–H⋯O hydrogen-bonds contributed by coordinated water molecules. The uncoordinated o-OOCC6H4-COFc ligands in 2 play a key role in the process of charge balance. FESEM images exhibited different surface appearances between the ligand and barium complexes, that is: flower-like HTCPA, branch-like o-HOOCC6H4-COFc, block-like complex 1 and corner-truncated cubes for complex 2. The allelopathic activity of the complexes and their corresponding ligands was evaluated against two herbaceous plants of barnyard grass and turnip (Raphanus sativus). All the tested compounds showed certain activity with good RI values. An antifungal bioassay was also carried out in vitro on three strains of Botrytis cinerea Pers., Glomerella cingulata Schr and Cytospora sp. Complex 1 and HTCPA can work against all three tested fungi, whereas o-HOOCC6H4-COFc and 2 only worked for Botrytis cinerea Pers. The complex presented in this paper has potential applications in weed control, and this work provides an experimental basis for future studies on Ba-based pesticides.

研究领域: 无机化学 · 金属配合物化学 · 农业化学 · 晶体工程 · 植物生理学 · 农药学 · 生物活性评估
✓ 已验证 DOI 高影响因子
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BioEnergy Research · 2015 ·Vol. 8 ·期 3 ·1263-1274 · IF 3.541

Selective Production of Levoglucosenone from Catalytic Fast Pyrolysis of Biomass Mechanically Mixed with Solid Phosphoric Acid Catalysts

Zhang Zhi-bo,Lu Qiang,Ye Xiao-ning,Wang Ti-peng,Wang Xian-hua,Dong Chang-qing

Solid phosphoric acid (SPA) catalysts with different carriers were prepared and used for catalytic fast pyrolysis of poplar wood to produce levoglucosenone (LGO), a valuable anhydrosugar derivative that can be used in various organic synthesis applications. Pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) experiments were performed to evaluate the catalytic capabilities of these catalysts under different reaction conditions. The results indicated that SPA catalyst prepared with the SBA-15 carrier exhibited the best catalytic capability for selectively producing LGO. Both the catalytic pyrolysis temperature and catalyst-to-biomass ratio affected the pyrolytic products greatly. The maximal LGO yield reached as high as 8.2 wt% from poplar wood, obtained at the pyrolysis temperature of 300 °C and the catalyst-to-biomass ratio of 1. The by-products during the catalytic pyrolysis process were mainly acetic acid (AA) and furfural (FF). In addition, the SPA catalyst possessed better catalytic capability than the liquid phosphoric acid (H 3 PO 4 ) catalyst to produce LGO.

研究领域: 生物能源 · 催化化学 · 生物质转化 · 热解化学 · 绿色化学 · 可再生资源利用
✓ 已验证 DOI 高影响因子
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