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MOLECULES · 2018 ·Vol. 24 ·期 1 ·128 · IF 3.098

Chemical Property Changes and Thermal Analysis during the Carbonizing Process of the Pollen Grains of Typha

Mingliang Gao,Beihua Bao,Yudan Cao,Mingqiu Shan,Fangfang Cheng,Miao Jiang,Peidong Chen,Li Zhang

Carbonized pollen grains of Typha (CPT) were widely used in clinical for antithrombosis, wound and bleeding in China. In order to ensure the role of drugs, it is very important to control the quality of drugs. However, there is a lack of monitoring methods in the process of charcoal preparation. To characterize the process of CPT, we used thermal analysis, scanning electron microscope (SEM), color measurement, Fourier transform infrared spectrometry (FTIR) and HPLC. In this study, 7 min was the optimal processing time and the heating process condition should be controlled under 272.35 ± 7.23 °C. This comprehensive strategy to depict the whole carbonizing process would provide new ideas for researches on quality control of Traditional Chinese Medicine (TCM) and processing theory of charcoal medicine.Keywords:pollen grains of Typha;thermal analysis;carbonizing process;Fourier transform infrared spectrometry (FTIR)

CAS / MDL: 123-92-2 7664-38-2
研究领域: 药学 · 热分析 · 中医 · 光谱学
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RSC Advances · 2022 ·Vol. 12 ·期 6 ·3454-3464 · IF 4.036

Tannic acid induces dentin biomineralization by crosslinking and surface modification

Weijing Kong,Qiaolin Du,Yinan Qu,Changyu Shao,Chaoqun Chen,Jian Sun,Caiyun Mao,Ruikang Tang,Xinhua Gu

It is currently known that crosslinking agents can effectively improve the mechanical properties of dentin by crosslinking type I collagen. However, few scholars have focused on the influence of crosslinking agents on the collagen-mineral interface after crosslinking. Analysis of the Fourier transform infrared spectroscopy (FTIR) results showed that hydrogen bonding occurs between the tannic acid (TA) molecule and the collagen. The crosslinking degree of TA to collagen reached a maximum 41.28 ± 1.52. This study used TA crosslinked collagen fibers to successfully induce dentin biomineralization, and the complete remineralization was achieved within 4 days. The crosslinking effect of TA can improve the mechanical properties and anti-enzyme properties of dentin. The elastic modulus (mean and standard deviation) and hardness values of the remineralized dentin pretreated with TA reached 19.1 ± 1.12 GPa and 0.68 ± 0.06 GPa, respectively, which were close to those of healthy dentin measurements, but significantly higher than those of dentin without crosslinking (8.91 ± 1.82 GPa and 0.16 ± 0.01 GPa). The interface energy between the surface of collagen fibers and minerals decreased from 10.59 mJ m−2 to 4.19 mJ m−2 with the influence of TA. The current work reveals the importance of tannic acid crosslinking for dentin remineralization while providing profound insights into the interfacial control of biomolecules in collagen mineralization.

研究领域: 牙科材料 · 生物材料 · 生物矿化 · 胶原科学 · 材料科学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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Gels · 2025 ·Vol. 11 ·期 9 ·697 · IF 5.3

Double-Network Hydrogels via Hybrid Strategies: Potential in Large-Scale Manufacturing for Colorimetric Indicator

Ningli An,Jiwen Liu,Wentao Zhou,Qing He,Jianan Li,Yali Xiong

Biological hydrogels are widely available in terms of raw material sources and can be processed and molded using relatively simple techniques. Hydrogels can offer abundant three-dimensional, water-containing channels that facilitate the reaction between gases and dye, making them the preferred choice for the solid support layer in colorimetric indicators. However, biomass hydrogels exhibit inferior mechanical properties, making them unsuitable for large-scale manufacturing processes. In this study, four dual-network composite hydrogels Agar/Gelatin, Sodium Alginate/Agar, Sodium Alginate/Poly (vinyl alcohol), Sodium Alginate/Gelatin (AG/Gel, SA/AG, SA/PVA and SA/Gel) prepared through hybrid strategies. Furthermore, the influence of the dual-network structure on the mechanical properties and ammonia response was systematically investigated, using microscopy and Fourier transform infrared spectroscopy (FTIR) characterization method. The experimental results demonstrate that the incorporation of SA into original hydrogel matrices can significantly enhance both the mechanical and ammonia response performance due to the secondary topological network structure. The interpenetrating double network structure was effectively regulated through the calcium ion cross-linking process. The color difference threshold of SA/PVA’s response to ammonia gas is 10, it holds promise for rapid detection applications. The SA/Gel composite hydrogel exhibits excellent mechanical robustness and toughness. The tensile strength of the SA/Gel sample is 11 times that of a single gel, and the toughness is 80 times greater, suggesting its suitability for large-scale manufacturing of colorimetric indicator.

CAS / MDL: 9000-70-8
研究领域: 材料科学 · 高分子化学 · 传感器技术 · 生物医学工程
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Energies · 2019 ·Vol. 12 ·期 19 ·3726 · IF 2.707

An Investigation on the Function of Mud Cakes on the Inhibition of Low Molecular Inhibitor for Water-Based Drilling Fluids

Wenxin Dong,Xiaolin Pu,Biao Ma

The major low molecular inhibitors showed inhibition in the hydration of clay in the laboratory for water-based drilling fluids, according to the principle of intercalation adsorption. However, inhibitors have failed and caused serious engineering accidents in drilling oil and natural gas. This paper investigated the transmission of several of drilling fluids to indicate whether low molecular inhibitor for drilling can effectively inhibit the wellbore hydration. The inhibition of drilling fluid with the plugging of mud cakes, was significantly weakened based on the hydration expansion of cores and cutting recoveries. The residual contents of inhibitors were determined with the precolumn derivation of high-performance liquid chromatography (HPLC) analysis and were chartered with Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) analysis in the structure of the derivative. The clogging behavior of the mud cake was described by environmental scanning electron microscopy (ESEM). Experiments show that 40 wt% to 90 wt% by weight of the corrosion inhibitor cannot pass through the mud cake in the dynamic filtration of the drilling fluid. The mud cake can be further divided into a nanostructure layer, a homogeneous layer and an anisotropic layer with different permeability. Most inhibitors should be limited to the nanostructure layer and the homogeneous layer.Keywords:low molecular inhibitors;drilling fluids;mud cake;plugging

研究领域: 石油工程 · 化学工程 · 材料科学
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JOURNAL OF PHYSICAL CHEMISTRY B · 2025 · IF 2.9

Salt-Tuned Mechanical Properties of Hydrogels: An O:H–O Bond Perspective

Haiyang Huang,Yong Zhou,Ling Xie,Bing Li,Wenlong Wang,Xinjuan Liu,Yongli Huang,Chang Q. Sun,Biao Wang

Hydrogels are versatile functional materials with applications in biomedical devices, sensors, and energy systems. However, tailoring their mechanical properties remains a critical challenge for expanding their practical utility. Here, the mechanical properties of poly(vinyl alcohol) (PVA) hydrogels prepared via the freeze–thaw method were effectively tailored through the incorporation of various chloride salts. This study reveals the molecular mechanisms by which salt ions influence the water structure, polymer chain interactions, and freezing behavior to modulate hydrogel performance. Using Raman spectroscopy, X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FTIR), we elucidate how cation-specific effects alter the crystallinity, cross-linking density, and hydrogen bond network in the hydrogels. Hydrogels containing K+ exhibited superior rigidity and toughness due to enhanced crystallinity and optimized water–polymer interactions, while hydrogels of Mg2+ and Ca2+ had much lower modulus and adhesion strength since the divalent ions reduced freezing points resulting in reduced polymer aggregation. These findings provide a molecular-level understanding of the salting effects on hydrogel properties, offering new insights into designing materials with tunable mechanical performance for diverse applications.

CAS / MDL: 7447-40-7
研究领域: 材料科学 · 高分子科学 · 机械工程 · 生物医学工程 · 物理化学
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JOURNAL OF VINYL & ADDITIVE TECHNOLOGY · 2022 ·Vol. 28 ·期 4 ·719-725 · IF 2.297

Rheological properties and dynamic thermal stability of PVC/La L2/Ca-Zn composite stabilizer

Deling Li,Congcong Luo,Bing Yao,Yue Ding,Jizhen Ren

Lanthanum complex with curcumin (La L 2 )/Ca-Zn composite stabilizer was prepared using La L 2 and Ca-Zn stabilizer, in which Ca-Zn stabilizer was obtained from calcium stearate and zinc stearate at their mass ratio of 5:1. The rheological properties and dynamic thermal stability of polyvinyl chloride (PVC) stabilized by La L 2 /Ca-Zn composite stabilizers were estimated through a torque rheometer. The degraded fragments obtained from the torque experiments were measured by Fourier-transform infrared spectroscopy (FTIR) and ultraviolet–visible (UV-vis) spectroscopy. La L 2 had an effective synergistic effect with Ca-Zn stabilizer. Compared with La L 2 , La L 2 /Ca-Zn composite stabilizer could more significantly improve the rheological properties and dynamic thermal stability of PVC. An optimal synergistic effect could be observed when the mass ratio of La L 2 with Ca-Zn stabilizer was about 8:2, in which the plasticizing torque and equilibrium torque of PVC was 33.3 N m and 22.5 N m, respectively, and its dynamic thermal stabilizing time was 25.1 min. The possible thermal stability mechanism of La L 2 /Ca-Zn composite stabilizer for PVC was suggested based on the evaluation of FTIR spectroscopy and UV-vis spectroscopy.

CAS / MDL: 9002-86-2
研究领域: 材料科学 · 高分子科学 · 化学工程
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JOURNAL OF LOSS PREVENTION IN THE PROCESS INDUSTRIES · 2021 · IF 3.66

Effects of the feeding procedure on the thermal behaviors of autocatalytic esterifications in semibatch processes

Qiang Chen,Yuqing Ni,Jun Liang,Lei Ni,Juncheng Jiang,Yong Pan,Qingsheng Wang

Esterification reactions between anhydrides and alcohols catalyzed by sulfuric acid have broad applications in the food, cosmetic, and pharmaceutical industries. However, the exothermic behavior cannot be well explained, especially in semibatch reactors with different feeding procedures. In this study, a series of esterification processes in semibatch systems were conducted with a wide range of feeding rates with two different substrates. The structures of initial catalytic substrates were characterized using in situ Fourier Transform Infrared (FTIR) spectroscopy. A total of 11 reaction pathways, including those for the initial activation of substrates and the subsequent reactions of the feeding process, were calculated by the density functional theory (DFT) method. Three possible catalytic cycles of the esterification with specific acid catalysis, protonated intermediate, and protonated intermediate and H 2 O, were established for the semibatch esterification reaction based on calculated results and experimental evidence. Thermal safety parameters such as reaction enthalpy ( Δ H r ΔHr ), adiabatic temperature rise ( Δ T r , a d ΔTr,ad ), and maximum temperature of the synthetic reaction (MTSR) were determined based on Wilson equation used to calibrate mixing heat. The results reveal that mixing heat was 2.5 kJ/mol with same mole ratio of n -butanol ( n B) and propionic anhydride (PA). The reactions started by PA are dominant, no matter whether the substrate is n B or PA. The initial reaction rate is restricted by the low concentration of catalyst and active reactant when n B is used as substrate, which lead to significant reactant accumulation with high MTSR of approximately 160 °C. Furthermore, feeding n B into PA allows a controllable increase in the Δ T r , a d ΔTr,ad realized by changing the feeding rate and limiting the accumulation of reactant.

CAS / MDL: 590-01-2 123-62-6
研究领域: 化学工程 · 物理化学 · 过程安全
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Chemical Engineering and Processing-Process Intensification · 2018 · IF 2.826

Preparation of Fe(III)-MOFs by microwave-assisted ball for efficiently removing organic dyes in aqueous solutions under natural light

Ding Chen,Peng-fei Feng,Fu-hua Wei

Fe-based metal-organic frameworks(Fe(III)-MOFs)were synthesized by Fe 2 (SO 4 ) 3 and trimesic acid using microwave-assisted ball milling method. The structure of the Fe(III)-MOFs was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier transform infrared spectrometry (FTIR). The thermostability of the MOFs was analyzed by thermogravimetric analysis (TGA). Fe(III)-MOFs were added in aqueous solutions to remove organic dyes. The removal efficiencies of Orange II, CR and MB reached 95.9%, 98.7%, 95.7% respectively at 10℃ and reached 97.7%, 99.7%, 97.5% respectively at 35℃ in 300 min.

研究领域: 材料科学 · 环境科学 · 化学
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JACS Au · 2022 · IF 0

Plasma-Catalytic CO2 Hydrogenation over a Pd/ZnO Catalyst: In Situ Probing of Gas-Phase and Surface Reactions

Yuhai Sun,Junliang Wu,Yaolin Wang,Jingjing Li,Ni Wang,Jonathan Harding,Shengpeng Mo,Limin Chen,Peirong Chen,Mingli Fu,Daiqi Ye,Jun Huang,Xin Tu

Plasma-catalytic CO2 hydrogenation is a complex chemical process combining plasma-assisted gas-phase and surface reactions. Herein, we investigated CO2 hydrogenation over Pd/ZnO and ZnO in a tubular dielectric barrier discharge (DBD) reactor at ambient pressure. Compared to the CO2 hydrogenation using Plasma Only or Plasma + ZnO, placing Pd/ZnO in the DBD almost doubled the conversion of CO2 (36.7%) and CO yield (35.5%). The reaction pathways in the plasma-enhanced catalytic hydrogenation of CO2 were investigated by in situ Fourier transform infrared (FTIR) spectroscopy using a novel integrated in situ DBD/FTIR gas cell reactor, combined with online mass spectrometry (MS) analysis, kinetic analysis, and emission spectroscopic measurements. In plasma CO2 hydrogenation over Pd/ZnO, the hydrogenation of adsorbed surface CO2 on Pd/ZnO is the dominant reaction route for the enhanced CO2 conversion, which can be ascribed to the generation of a ZnOx overlay as a result of the strong metal–support interactions (SMSI) at the Pd–ZnO interface and the presence of abundant H species at the surface of Pd/ZnO; however, this important surface reaction can be limited in the Plasma + ZnO system due to a lack of active H species present on the ZnO surface and the absence of the SMSI. Instead, CO2 splitting to CO, both in the plasma gas phase and on the surface of ZnO, is believed to make an important contribution to the conversion of CO2 in the Plasma + ZnO system.

CAS / MDL: 10196-18-6
研究领域: 催化化学 · 等离子体化学 · 环境科学 · 可持续能源
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JOURNAL OF MATERIALS SCIENCE · 2023 ·Vol. 58 ·期 25 ·10359-10369 · IF 4.5

Reinforcing the mechanical properties of bamboo fiber/low density polyethylene composites with modified bamboo-woven structure

Liu Shujuan,Liu Lijuan,Yang Kangli,Yuan Zhiqing,Li Xinyi,Li Cancheng,Meng Shoutong

In order to improve the environmental problems caused by the extensive use of plastics, this paper introduced a new strategy to add and modify the physical structure, which could not only reduce the use of plastics, but also improve the mechanical properties of bamboo plastic composites. In this work, the bamboo-woven structure was introduced into the bamboo fiber/low density polyethylene (LDPE) composites to enhance the mechanical properties. Besides, to enhance the interfacial compatibility, maleic anhydride (MA) and polyvinyl alcohol (PVA) were used to modify LDPE and bamboo-woven structure, respectively. The mechanical properties of the prepared PVA-bamboo-woven structure/bamboo fiber/MA-LDPE composites were greatly improved. The bamboo plastic composites were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy, water contact angle (WCA) test and mechanical property test. The results showed that the bamboo-woven structure/bamboo fiber/MA-LDPE composite has superior properties at 45% bamboo fiber content. The tensile strength reached to 33.842 MPa, which was increased by 65.01% compared to the bamboo fiber/MA-LDPE composites, and the bending strength reached to 36.6585 MPa increased by 81.46% in relation to the bamboo fiber/MA-LDPE composites. In addition, even a large number of hydrophilic bamboo fibers and bamboo-woven structure were carried by the composites, a good hydrophobicity was still maintained and the WCA reached to 93.71°. The composites with excellent mechanical properties and hydrophobicity provided a reference for the use of bamboo fibers in environmentally friendly packaging materials.

研究领域: 材料科学 · 高分子科学 · 环境工程 · 生物复合材料 · 机械工程
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Journal of Macromolecular Science Part A-Pure and Applied Chemistry · 2014 · IF 0.74

Synthesis and Characterization of Comb-like Methoxy Polyethylene Glycol-grafted Polyurethanes via ‘Click’ Chemistry

Yunyan Xue,Dandan Ma,Tianzhu Zhang,Siyan Lin,Shengnan Shao,Ning Gu

In this study, a series of comb-like methoxy polyethylene glycol (MPEG) functionalized polyurethanes (PUs) (PU–g–MPEG) were successfully prepared via ‘click’ chemistry and polyaddition reaction. The copper catalyzed Huisgen 1,3-dipolar cycloaddition was firstly carried out between 3,5-bis(hydroxymethyl)-1-propargyloxybenzene (PBM) and methoxy polyethylene glycol azide (MPEG–N3) to obtain MPEGylated diol PBM (MPEG–PBM). Then, the comb-like PUs having MPEG located on the backbones (PU–g–MPEG) were synthesized through the polyaddition of MPEGylated diol PBM and hexamethylene diisocyanate (HDI). Fourier transform infrared (FTIR), 1H NMR spectroscopy, size exclusion chromatography (SEC), and thermo gravimetric analyses (TGA) were used to characterize these synthesized MPEG-functionalized comb-like PUs (PU–g–MPEG). Compared with PU without MPEG grafts, PU–g–MPEG show a better wettability.

研究领域: 高分子化学 · 材料科学 · 有机合成 · 表面化学
✓ 已验证 DOI 高影响因子
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FIBERS AND POLYMERS · 2020 ·Vol. 21 ·期 6 ·1229-1237 · IF 1.797

A Facile and Controllable Approach for Surface Modification of Wool by Micro-dissolution

Zhang Yiyi,Zhang Nan,Wang Qiang,Yu Yuanyuan,Wang Ping,Yuan Jiugang

Most modifications of wool focused on its surface due to the existence of the cuticle scales. For instance, chlorination, oxidation and protease treatments were used to break down or remove the scales. However, these modifications usually severely damaged the internal structure of wool. In this paper, a novel approach based on surface micro-dissolution was employed to modify the surface of wool to minimize the internal damage of wool, and improve the surface-related properties of wool. The micro-dissolution system used NaHSO 3 /urea to dissolve the scale layer of wool. After being micro-dissolved with NaHSO 3 /urea system, scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), fluorescence microscopy, Fourier transform infrared spectroscopy (FTIR), and the Allwörden reaction were utilized to characterize the treated wool. Furthermore, felting shrinkage, strength loss and wettability of the treated wool were determined. The results showed that NaHSO 3 /urea system could dissolve the scale layer from outside to inside. The fluorescence microscopic images further indicated that low concentration of NaHSO 3 /urea system can dissolve the surface of wool without the serious damage of internal structure. Moreover, the micro-dissolution system can be controlled to dissolve the scale layer on the surface of wool slightly by adjusting the reaction conditions. The presented method is simple, easy to operate, and economical, thereby can open up new directions for the surface modification of wool.

CAS / MDL: 69-78-3
研究领域: 材料科学 · 纺织工程 · 化学工程
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