APPLIED ORGANOMETALLIC CHEMISTRY
·
2019
·Vol. 33
·期 5
·e4850
·
IF 3.259
Mingliang Ma,Yuying Yang,Yanyan Liu,Wenting Li,Guopeng Chen,Yong Ma,Ping Lyu,Shunhe Li,Yubao Wang,Guanglei Wu
In this paper, a simple route for palladium (Pd) nanoparticles attached to the surface of hollow magnetic Fe 3 O 4 /P (GMA-DVB)-polyethyleneimine (PEI) microspheres was established. Due to the large amount of imidogen groups and tertiary amine groups presenting in the PEI, Pd 2+ ions could be anchored to the support by complexation with a polyfunctional organic ligand. Thereafter, a magnetic Pd catalyst having a high loading amount and good dispersibility was obtained by reducing Pd 2+ ions. Afterwards, the prepared catalyst was characterized by TEM, SEM, FTIR, XRD, TGA, VSM, and UV–vis in detail. Ultimately, their catalytic activity was evaluated using the reduction of 4-nitrophenol (4-NP). Research showed that the Fe 3 O 4 /P (GMA-DVB)-PEI/Pd catalyst possessed high catalytic performances for the reduction of 4-NP with a conversion rate of 98.43% within 540 s. Furthermore, the catalyst could be easily recovered and reused at least for nine successive cycles.
研究领域:
材料科学
·
催化化学
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产品关联
DOI
高影响因子
MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Jing Zhou,Hongyu Ning,Haixing Wang,Sen Zhao,Yu Xu,Yilei Fan,Zhongping Huang,Jianhong Gao
Cannabis is the most frequently abused drug worldwide, and the number of cannabis users is still growing. The high lipophilicity of cannabinoids results in extremely low concentrations in wastewater, which poses difficulties and challenges for monitoring cannabinoids. In this study, a hyperbranched mixed-mode anion exchange magnetic adsorbent Fe 3 O 4 @poly(GMA/DVB-WAX) was designed based on the structural characteristics of cannabinoids, which was prepared through copolymerization of glycidyl methacrylate (GMA) and divinylbenzene (DVB) on the surface of oleic acid coated Fe 3 O 4 microspheres followed by hyperbranched modification with ethylenediamine (EDA) and 1,4-butanediol glycidyl ether (BDDGE). This magnetic solid-phase extraction (MSPE) adsorbent can selectively extract four cannabinoids, Δ 9 -tetrahydrocannabinol (THC), cannabidiol (CBD), cannabinol (CBN), 11-nor-9-carboxy-Δ 9 -tetrahydrocannabinol (THC-COOH), from wastewater through the synergistic effects of hydrophobic interactions, electrostatic interactions, π-π stacking interactions, and hydrogen bonding interactions. The entire extraction time of the adsorbent only takes five minutes and the extraction recovery rates were in the range of 69.4 %-94.0 % for four cannabinoids after the MSPE procedure optimization. An MSPE-UHPLC-MS/MS quantitative method for determination of four cannabinoids in wastewater was established and validated. The results showed that this method had a good linearity within the range of 0.5–100 ng/L (r 2 > 0.9962). The limits of detection and the limits of quantification were 0.17–0.33 ng/L and 0.50–1.00 ng/L, respectively. The proposed MSPE-UHPLC-MS/MS method based on Fe 3 O 4 @poly(GMA/DVB-WAX) is a convenient, sensitive and reliable strategy and has great application prospects in the analysis of trace cannabinoids in wastewater.
研究领域:
分析化学
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环境科学
·
毒理学
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2021
·
IF 7.312
Xiao-Han Pan,Ling-Xiao Fu,Huan Wang,Yi Xue,Jian-Hua Zu
A novel sulfydryl-functionalized adsorbent PP-g-GMA@MEA for recovery of Ag(I) was synthesized by γ-ray induced simultaneous grafting of glycidyl methacrylate (GMA) onto polypropylene (PP) non-woven fabric, followed by ring-opening processes with mercaptoethylamine (MEA). The obtained adsorbents before and after adsorption of Ag(I) were fully characterized by SEM, EDS, FT-IR spectra, XRD and XPS. Batch adsorption experiments were carried out to evaluate adsorption abilities of the adsorbents under high acidity. The adsorption kinetics of Ag(I) were well fitted with pseudo-second-order kinetics model. The maximum adsorption capacity calculated by the Langmuir isotherm model was 262.51 mg/g at 25 °C. EDS, XRD and XPS analyses confirmed the mechanism of adsorption under high acidity was chelating reaction between -SH and Ag(I) and ion exchange adsorption towards [Ag(NO 3 ) 2 ] −1 . Through competitive adsorption tests, the PP-g-GMA@MEA was found remarkably selective towards Ag(I) when it coexisted with Cu(II), Co(II), Ni(II) and Cr(III) in high acidity medium. Therefore, the developed PP-g-GMA@MEA composite would be a promising adsorbent for Ag(I) recovery from industrial effluents.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY
·
2013
·Vol. 172
·期 2
·701-712
·
IF 1.893
Cui Yanjun,Chen Xia,Li Yanfeng,Liu Xiao,Lei Lin,Zhang Yakui,Qian Jiayu
Using emulsion copolymer of styrene (St), glycidyl methacrylate (GMA) and 2-hydroxyethyl methacrylate (HEMA) as seed latexes, the superparamagnetic polymer emulsion particles were prepared by seeded emulsion copolymerization of butyl methacrylate (BMA), vinyl acetate (VAc) and ethylene glycol dimethacrylate in the presence of the seed latexes and superparamagnetic Fe 3 O 4 /SiOx nanoparticles (or Fe 3 O 4 -APTS nanoparticles) through a two-step process, without addition of any emulsifier. The magnetic emulsion particles named P(St-GMA-HEMA)/P(BMA-VAc) were characterized by transmission electron microscope and vibrating sample magnetometry. The results showed that the magnetic emulsion particles held a structure with a thinner shell (around 100 nm) and a bigger cavity (around 200 nm), and possessed a certain level of magnetic response. The resulting magnetic emulsion particles were employed in the immobilization of lipase by two strategies to immobilized lipase onto the resulting magnetic composites directly (S-1) or using glutaraldehyde as a coupling agent (S-2), thus, experimental data showed that the thermal stability and reusability of immobilized lipase based on S-2 were higher than that of S-1.
研究领域:
材料科学
·
生物技术
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产品关联
DOI
PubMed
高影响因子
CELLULOSE
·
2024
·Vol. 31
·期 6
·4007-4023
·
IF 4.9
Xue Tong,Ma Ruijie,Zhang Xintian,Tao Wenwen,Wang Chaoxia,Yin Yunjie
Personal thermal management (PTM) textiles with heating or cooling capabilities are highly attractive because they offer individual comfort and contribute to lower energy consumption. However, due to the subjectivity of thermal comfort, developing adaptive and personalized PTM textiles remains a challenge. Here, we report a thermoresponsive cotton fabric (PMOG-cotton), which is prepared by a combination of ultraviolet-induced free radical polymerization and pad-dry-cure process. 2-(2-methoxyethoxy)ethyl methacrylate (MEO 2 MA) and oligo(ethylene glycol) methacrylate (OEGMA 475 ) are selected as thermoresponsive monomers, while glycidyl methacrylate (GMA) is chosen as the linking monomer for copolymerization. The lower critical solution temperature (LCST) of P(MEO 2 MA-co-OEGMA 475 -co-GMA) can be precisely regulated by adjusting the dosage of OEGMA 475 . Furthermore, PMOG-cotton demonstrates a reversible transition between hydrophobic and hydrophilic states in response to variations in external temperature (T > LCST, hydrophobic; T < LCST, hydrophilic). This transition can be sustained for a minimum of 5 cycles and 50 rubbing cycles. PMOG-cotton exhibits superior control over breathability and moisture permeability compared to raw cotton in response to temperature fluctuations. Compared to raw cotton, PMOG-cotton offers a 2.4 °C heating effect in cold environments and a 1.3 °C cooling effect in hot environments. This adaptive thermal management textile shows promise for delivering human thermal comfort in complex and dynamic environments.
研究领域:
材料科学
·
纺织工程
·
高分子化学
✓ 已验证
产品关联
DOI
高影响因子
COMPUTATIONAL MATERIALS SCIENCE
·
2026
·
IF 3.7
Yuanchao He,Guangxiang Zhang,Huijia Lu,Xiaorong Wang,Ying Yu,Shiguang Wan,Xin Liu,Miao Xie,Guiyan Zhao
This study utilized molecular dynamics simulations to incorporate a poly(lactic acid) (PLA) matrix, poly(butylene adipate-co-terephthalate) modified with glycidyl methacrylate (PBAT-g-GMA), and thermoplastic starch (TPS) into an amorphous unit cell via a one-step blending method. Additionally, five PLA/PBAT-g-GMA/TPS (70/30/0, 70/25/5, 70/20/10, 70/15/15, 70/10/20) amorphous unit cells were created using a stepwise blending method. The radial distribution functions, hydrogen bond distribution, cohesive energy density, mixing energy, and diffusion coefficient of the blend components were analyzed. The optimal composition, identified through simulations, was subsequently prepared, and its glass transition temperature (T g ) was determined using differential scanning calorimetry (DSC). The fracture surface was examined via scanning electron microscopy (SEM). Results showed that the one-step blending model did not form a distinct core-shell interface, whereas higher PBAT ratios in the stepwise blending model exhibited clearer core-shell interfaces. The 70/20/10 composition model exhibited the highest mixing energy (1067.0 kcal/mol). The number of hydrogen bonds at the PBAT-TPS interface was maximized in this model, indicating the strongest interfacial interaction. The predicted T g of the 70/20/10 composition model was 59.9 °C, differing by only 0.6 °C from the measured value. The core-shell structure was observed on the frozen fracture surface, confirming the reliability of the model predictions. This study systematically analyzed the formation, distribution, and interaction of the core-shell interface in the PLA-based ternary blend system using molecular dynamics simulations and multi-indicator analysis. An optimal blending ratio was identified, providing a theoretical foundation for future material design and optimization.
✓ 已验证
产品关联
DOI
高影响因子
TALANTA
·
2020
·
IF 5.339
Muhammad Mujahid Ali,Dilshad Hussain,Bin Xu,Tangqiang Sun,Zhenxia Du
Cis -diol compounds are class of biomolecules including nucleosides , glycoproteins , saccharides , and nucleotides, which play vital roles in various biological processes. Due to low abundances of these species in the complex biological samples, their identification and analysis is difficult. Boronate affinity materials are commonly used for the isolation and enrichment of cis -diol compounds, due to their unique, facile and selective enrichment mechanism. In this study we report a selective approach to extract nucleosides, glycopeptides and glycoproteins using boronic acid functionalized GMA-MAA-DVB polymer. This novel polymer, reported for the first time in proteomics, have high BET surface area (132.8447 m 2 g −1 ) which contribute to efficient enrichment and average pore size (20.3449 nm) to facilitates the nano confinement effect for strong interactions. Hydrophilic character of methacrylic acid and diethylenetriamine , along with inherent affinity of boronic acid for glycosylated biomolecules result in selectivity up to 1:500 for peptides and 1:1000 for glycoprotein. Binding constant for cis -diol compounds are in the range of 10 −4 to 10 −6 M and theoretical binding capacity up to 85 mg g −1 for HRP and 180 mg g −1 for IgG, respectively. Furthermore, boronic acid functionalized polymer (BFP) enrich glycoproteins and glycopeptides in range of 1 pg mL −1 and 0.04 ng mL −1 with S/N ≥ 3. Finally, material is applied to enrich the glycoproteins from healthy human saliva sample and six glycoproteins are identified.
研究领域:
生物化学
·
蛋白质组学
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产品关联
DOI
PubMed
高影响因子
TALANTA
·
2020
·
IF 5.339
Shuxiang Li,Zongying Li,Feifang Zhang,Huiliang Geng,Bingcheng Yang
We describe a novel polymer-based zwitterionic stationary phase for hydrophilic interaction chromatography (HILIC). It is prepared by chemical modification of poly (glycidyl methacrylate-divinylbenzene) (GMA-DVB) by converting epoxide groups of microsphere surface to diol groups via hydrolysis, then clicking cysteine onto the microsphere with pendant double bonds of microsphere surface via “thiol-ene” click chemistry. The phase has been characterized by scanning electron micrograph, elemental analysis and zeta potential measurement. Diol and zwitterionic group (carboxylate and amine group associated with cysteine) onto the surface of GMA-DVB microspheres make them possess good hydrophilicity , as supported by effective separation towards common polar analytes. It shows good stability at alkaline solution (e.g. pH 10) and negligible bleed (e.g. only 1.7-fold blank and ~55-fold lower than a commercial silica-based polar phase tested with the minimal bleed level). Such phase exhibits specific separation selectivity to ionic analytes and simultaneous separation of anions and cations is achieved in the retention order of I − < NO 3 − < Choline < Br − < Cl − < K + < Na + .
研究领域:
分析化学
·
材料科学
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2026
·
IF 5.4
Xinrui Chen,Yudong Shang,Peng Gu,Yan Ren,Shihua Li,Siyu Fang,Huajie Zhong,Linhe Zhu,Jianhui Mei,Yuanlin Wu,Suqing Chen
In response to the growing global restrictions on fluorinated compounds, this study aims to develop an environmentally friendly and durable fluorine-free water-repellent finishing agent for textiles. A series of cross-linked acrylic emulsions were synthesized using MMA as the hard monomer, BA as the soft monomer, ODA as the hydrophobic functional monomer, and GMA and NMA as the crosslinking monomers. The effects of GMA content on the water repellency and emulsion properties were systematically investigated. To further enhance the hydrophobic performance, SiO₂ and TiO₂ nanoparticles were introduced through both composite emulsification and a step-by-step finishing method. The results showed that the optimal GMA content effectively improved the gelation rate, conversion rate, and contact angle of the treated fabric. Nanoparticle modification increased surface roughness, improved wash durability, and enhanced thermal stability, as confirmed by TG and DSC analyses. Among the modifiers tested, PTES achieved the best hydrophobic enhancement with a maximum contact angle of 146 °. Compared with untreated fabric, the spray grade increased from 0 to 4, and the abrasion resistance was markedly improved. This fluorine-free water-repellent system provides a promising alternative to traditional fluorinated agents, offering high water repellency, thermal stability, and fluorine-free and environmentally preferable.
✓ 已验证
DOI
高影响因子
ACS Applied Polymer Materials
·
2024
·
IF 4.4
Bowen Zhang,Yiqi Zhang,Jiufu Zhu,Zhanchen Cui,Wei Wang,Zuosen Shi
High performance polymeric dielectrics are of critical importance for obtaining high carrier mobility and realizing low operating voltage in OTFTs. In this work, copolymers poly(methyl methacrylate) containing 4-fluorostyrene monomer were used as insulating layers for OTFTs devices of C10-DNTT. With the increase of 4-fluorostyrene, the threshold voltage shifted positively, and the random copolymer poly(4-fluorostyrene–methyl methacrylate–glycidyl methacrylate)-5 (P(FSt-co-MMA-co-GMA)-5) exhibited a threshold voltage lower to 1.8 V, a hole mobility of up to 0.518 cm2 V–1 s–1, and a dielectric constant value of 5.66. XRD spectra reveal that C10-DNTT has the best morphology at (001) peak as the dielectric copolymer contains 5% 4-fluorostyrene monomer.
研究领域:
材料科学
·
电子学
·
高分子化学
✓ 已验证
DOI
高影响因子
APPLIED ORGANOMETALLIC CHEMISTRY
·
2018
·Vol. 33
·期 2
·e4708
·
IF 3.581
Mingliang Ma,Yuying Yang,Dili Liao,Ping Lyu,Jinwei Zhang,Jianli Liang,Lizhi Zhang
A strategy has been developed for the synthesis, characterization and catalysis of magnetic Fe 3 O 4 /P(GMA-EGDMA)-NH 2 /HPG-COOH-Pd core-shell structure supported catalyst. The P(GMA-EGDMA) polymer layer was coated on the surface of hollow magnetic Fe 3 O 4 microspheres through the effect of KH570. The core-shell magnetic Fe 3 O 4 /P(GMA-EGDMA) modified by -NH 2 could be grafted with HPG. Then, the hyperbranched glycidyl (HPG) with terminal -OH were modified by -COOH and adsorbed Pd nanoparticles. The hyperbranched polymer layer not only protected the Fe 3 O 4 magnetic core from acid–base substrate corrosion, but also provided a number of functional groups as binding sites for Pd nanoparticles. The prepared catalyst was characterized by UV–vis, TEM, SEM, FTIR, TGA, ICP-OES, BET, XRD, DLS and VSM. The catalytic tests showed that the magnetic Fe 3 O 4 /P(GMA-EGDMA)-NH 2 /HPG-COOH-Pd catalyst had excellent catalytic performance and retained 86% catalytic efficiency after 8 consecutive cycles.
研究领域:
材料科学
·
催化化学
✓ 已验证
产品关联
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2024
·
IF 4.9
Chengmin Hou,Weimin Yan,Hanxiao Ma,Yuan Bai,Zhiting Yuan
Heavy metal ion (Cu(II)) wastewater will do great harm to human body and environment, and the adsorption materials used in traditional adsorption methods are easy to hydrolyze, resulting in secondary pollution to water. In this paper, an adsorption material poly(glycidyl methacrylate-random-hydroxyethyl methacrylate) grafted ferric oxide@starch (St/Fe 3 O 4 - g -p(GMA- r -HEMA)) was prepared, which had epoxy and hydroxyl group , easy to produce crosslinking, reduce the sensitivity of starch to pH and prevent hydrolysis. Infrared spectroscopy (FTIR), thermogravimetric analysis (TG), scanning electron microscopy (SEM) and magnetometer (VSM) were used to characterize the structure and morphology of the adsorbent. The adsorption properties of the adsorbent for removal of Cu(II) ions were studied via changing the experimental conditions, including the amount of adsorbent, Cu(II) ions solution concentration, pH value, adsorption time, adsorption temperature and so on. Under the optimal adsorption conditions of pH value 7, initial Cu(II) concentration 20 mg/L and adsorption time 160 min, the maximum unit adsorption capacity of St/Fe 3 O 4 - g -p(GMA- r -HEMA) was 94.15 mg/g, and the adsorption performance was good. The adsorption process followed Langmuirm model and second-order kinetic model , and was dominated by chemisorption . The thermodynamic model showed that the adsorption process of St/Fe 3 O 4 - g -p(GMA- r -HEMA) was endothermic. After 8 adsorption cycles, 93.5% of the first adsorption effect can still be retained, and the renewable performance had been improved.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）