MACROMOLECULAR BIOSCIENCE
·
2015
·Vol. 15
·期 10
·1411-1422
·
IF 3.851
Yan-Ling Luo,Mei Han,Feng Xu,Ya-Shao Chen,Yong-Qin Zhang
pH-Responsive H-type poly(methylacrylic acid- block -four hydroxyl terminated poly(butadiene-acrylobitrile)- block -poly(methylacrylic acid (PMAA 2 - b -HTPBN- b -PMAA 2 ) block copolymers were synthesized via atom transfer radical polymerization and the follow-up hydrolysis, and characterized by 1 H NMR, FT-IR and SEC . The block copolymers could self-assemble into nanoscale spherical core-shell micelle aggregates in aqueous solution, and the physicochemical properties depended on the system composition and pH media, with pH phase transition at 5.7–6.1. The copolymer micelle aggregates exhibited pH-triggered drug release and cytotoxicity, and could potentially be used as drug targeting release carriers.
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COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING
·
2025
·
IF 8.9
Kaiming Yang,Feifei Wang,Bingrui Shi,Zhenlong Zhang,Weixu Feng,Guoquan Qi,Hongxia Yan
Developing low-temperature curing and high-performance self-lubricating anticorrosion coatings is a challenge for solving energy waste and environmental problems caused by wear and corrosion. Herein, molybdenum disulfide/hexagonal boron nitride (MoS 2 /h-BN) heterojunction particles, prepared by an inexpensive, efficient and solvent-free ultrasonic-assisted ball milling method, are used as solid lubricants and corrosive media barrier. Meanwhile, hyperbranched polysiloxane with terminal epoxy groups (HSiEp) is utilized to improve both the dispersion of the particles and the interfacial bonding strength between the particles and the epoxy binder. Compared with neat epoxy coating, the average friction coefficient of 45.0 wt% MoS 2 /h-BN/6.0 wt% HSiEp/EP coating decreases from 0.38 to 0.19, while the coating resistance (R 1 ) increases from 9.98 × 10 5 Ω·cm 2 to 3.33 × 10 6 Ω·cm 2 . This is mainly attributed to the “soft-hard” particle synergy and the high barrier synergy of HSiEp and MoS 2 /h-BN heterojunction particles. This study provides a theoretical foundation for the development of low-energy-consumption and high-performance epoxy self-lubricating anticorrosion coatings.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2024
·
IF 3.8
Yu Su,Rong Fan,Jiabao Li,Yangxi Liu,Ziyuan Zheng,Xin Zhou,Xiang Feng,Yibin Liu,Hui Zhao,Xiaobo Chen,Xingong Zhang,Chaohe Yang,Hao Yan
Oxidation of fatty alcohols to fatty acids is still challenging due to the sluggish activation of the C–H bond over Au supported on reducible oxides with a coordination-saturated structure. Herein, we constructed an efficient interfacial Auδ−–OV–Ti structure by tuning the crystal forms of TiO2. Compared with TiO2-rutile exposed by (110) and (111) crystal facets, TiO2-anatase can exploit the defect (101) crystal facet to obtain rich oxygen vacancies (OV), inducing electron migration from TiO2-anatase support to Au species to form electron-rich Auδ− species. Specifically, the synergistic catalytic effect between the OV–Ti and Auδ− species greatly enhances the adsorption of alcohol and thereby overcomes sluggish activation of the C–H bond caused by the electron pushing effect triggered by long carbon chains. Consequently, the Au/TiO2-anatase catalyst shows excellent isooctyl alcohol conversion (69.5%) and isocaprylic acid selectivity (67.9%) under base-free conditions. The catalytic system is further extended to the oxidation of other fatty alcohols to fatty acids with excellent catalytic performance.
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ACS Sustainable Chemistry & Engineering
·
2021
·
IF 8.198
Changzhou Chen,Peng Liu,Haihong Xia,Jianchun Jiang,Xiaohui Yang,Minghao Zhou
Lignin is an abundant source of aromatics with low effective hydrogen-to-carbon ratio (H/Ceff), and the depolymerization of lignin provides significant potential for producing liquid products with an improved H/Ceff value. In this work, the catalytic conversion of lignin monomers, dimer, trimers, and realistic lignin over spherical MOF-derived NiMo@C catalysts was well established, to get liquid fuels with a higher H/Ceff. The optimal ratio of the Ni4Mo1@C catalyst exhibited good hydrodeoxygenation activity and stability for the hydrotreatment of lignin model compounds and lignin. The addition of Mo facilitated the decrease of the particle size of a spherical structure, strengthened the electron-transfer capability between metals Mo and Ni, and enhanced the acid strength. All of these factors contributed to higher hydrodeoxygenation activity in the hydrotreatment process. Up to 100% conversion and 90% yields of ethylcyclohexane and cyclohexanol with H/Ceff values of 2.0 and 1.667, respectively, were obtained. The Ni4Mo1@C catalyst achieved a decrease of the oxygen element and an increase of H/Ceff and HHV values. The physicochemical characterizations were performed by various means including X-ray diffraction (XRD), scanning electronic microscopy (SEM), transmission electron microscopy (TEM), H2-temperature-programmed reduction (H2-TPR), NH3-temperature-programmed desorption (NH3-TPD), pyridine-infrared spectroscopy (Py-IR), inductively coupled plasma emission spectrometer (ICP), and Raman and X-ray photoelectron spectroscopy (XPS) analyses, which definitely elucidated the formation of a synergistic effect between metals Mo and Ni. Additionally, a control experiment also illustrated the synergistic effect that facilitated the occurrence of the hydrotreatment process under lower temperatures after the addition of metal Mo. Based on the optimal reaction condition (240 °C, 4 h, 2.0 MPa H2), both lignin and its monomers/dimers/trimers could be effectively hydrotreated to afford liquid products with improved H/Ceff value compared to raw lignin.
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JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS
·
2017
·
IF 3.471
Yunwu Zheng,Fei Wang,Xiaoqin Yang,Yuanbo Huang,Can Liu,Zhifeng Zheng,Jiyou Gu
The main objective of this work was to study aromatics production via the catalytic pyrolysis upgrading of biomass using metal-loaded modified H-ZSM-5. M-ZSM-5 catalysts were prepared through the impregnation method with Zn, Ga, Ni, Co, Mg and Cu. The prepared M-ZSM-5 catalysts were evaluated by x-ray diffraction, thermal desorption spectroscopy and scanning electron microscopy. The properties, composition and product distribution of bio-oil were also analysed. Results showed that the M-ZSM-5 catalysts yielded a higher amount of non-condensable gas at the expense of the liquid yields. The Ga-ZSM-5 catalysts produced the highest yields of bio-oil (25.76 wt%), but the lowest amount of coke (22.08 wt%) compared with the unmodified ZSM-5 catalyst (33.38 wt%). The content of the single-ring aromatics prepared by using the Zn-ZSM-5 catalysts was the highest at 90.28 wt%, whereas that of the polycyclic aromatic hydrocarbon prepared by the Ni-ZSM-5 catalysts was the highest at 31.36 wt%. Moreover, the selectivity of the single-ring aromatic hydrocarbons, such as C7 and C8, were significantly affected by the use of the M-ZSM-5 catalysts. The Zn-ZSM-5 catalysts were the most selective for toluene and xylenes with contents of 36.52 wt% and 35.32 wt%, respectively, whereas the Co-based catalysts were the most selective for indene. The Ni-based catalysts can obviously improve the selectivities of benzene production and C10+ polycyclic aromatic hydrocarbons. Zn-ZSM-5 was the most effective catalyst that can be used in the production of aromatic hydrocarbons.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2016
·
IF 3.014
Chunli Zhang,Yi He,Fei Li,Haihui Di,Lei Zhang,Yingqing Zhan
A novel hybrid materials Fe 3 O 4 nanoparticles supported by hexagonal boron nitride (h-BN) is successfully prepared via mussel-inspired chemistry of dopamine by hydrothermal synthesis method. The surface modification and microstructure of h-BN-Fe 3 O 4 are characterized by FT-IR, XRD , XPS, SEM and TEM . The nano-Fe 3 O 4 obtain well dispersion supported by h-BN layer platform, and the h-BN-Fe 3 O 4 hybrid materials exhibit a remarkable superiority in enhancing the anticorrosion performance of epoxy coatings. The lamellar structural h-BN and nano-Fe 3 O 4 provide a significant synergistic effect in anticorrosion performance for epoxy composite coatings . In addition, the anticorrosion mechanisms of h-BN-Fe 3 O 4 are tentatively discussed.
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Journal of Materials Chemistry C
·
2025
·
IF 5.1
Rui Ding,Wenjuan Zhang,Shiva Pandeya,Xueqing Zhu,Kai Xu,Meixing Gui,Hongbing Wang,Ziliang Li,Qianqian Shang,Mahesh Kumar Joshi
The design of a double Z-type heterojunction represents a promising strategy in photocatalysis to achieve superior charge carrier separation, increased light-harvesting capability, and consequently, a higher photocatalytic reaction rate. Herein, a novel ternary heterojunction with direct dual Z-scheme configuration, g-C3N4/In2S3/In2O3 photocatalyst, was synthesized using a chemical bath and facile calcination process. The XRD, SEM-EDS and XPS results confirmed the successful integration of g-C3N4, In2S3, and In2O3 with preserved crystalline phases. Photocatalytic performances of the ternary composite were evaluated via two effective routes, such as methyl orange (MO) degradation and hydrogen (H2) generation, benchmarked against the pristine g-C3N4 and the g-C3N4/In2S3 and In2S3/In2O3 binary composite, revealing that the in-situ growth of In2O3 onto the g-C3N4/In2S3 composite contributed to the remarkable enhancement of their photocatalytic activity. The photodegradation process follows the pseudo-first order reaction kinetics. The ternary g-C3N4/In2O3/In2S3 heterojunction exhibited 94.8% degradation efficiency of MO with a corresponding rate of 23.4×10-3 min-1, 4.8 times higher than the pristine g-C3N4, and excellent photocatalytic activity in five consecutive cycles. Similarly, the g-C3N4/In2S3/In2O3 heterojunction exhibited a rate constant of ~2.4 mmol h−1 g−1 for H2 generation. This superior enhancement was attributed to the dual Z-scheme charge transfer mechanism. The formation of direct dual Z-scheme heterojunction improved the light harvesting, minimized electron hole recombination, and efficiently facilitated the separation of charge carriers. This work provided a mechanistic insight for engineering multifunctional heterojunction for environmental remediation and pollutant mitigation.
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高影响因子
ADVANCED SYNTHESIS & CATALYSIS
·
2017
·Vol. 359
·期 13
·2215-2221
·
IF 5.646
Wenhui Zhu,Yingcai Ding,Zhaogang Bian,Ping Xie,Baojun Xu,Qiujie Tang,Wei Wu,Aihua Zhou
Sulfenylation is an important transformation to generate C−S bonds in organic synthesis. Here, two three-component synthetic protocols have been developed by using imidazo[1,2- a ]pyridine, inorganic, odorless S 8 and alcohols or arylboronic acids as reactants to make alkylthio-/arylthio-substituted imidazo[1,2- a ]pyridine derivatives via C( sp 2 )–H functionalization. The reactions proceeded with high efficiency and broad functional group tolerance, affording the products regioselectively and in good yields.
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BMC Chemistry
·
2019
·Vol. 13
·期 1
·1-15
·
IF 0
Guo J.,Ma Yu L.,Yu Jia Y.,Gao Yu J.,Ma Ning X.,Wu Xiao Y.
Herein, 2-(2-methoxyphenoxy)-1-phenylethanol (β- O -4), 2-methoxyphenyl anisole (α- O -4) and 4-phenoxyphenol (4- O -5) were selected as typical lignin model compounds. Given the effectiveness of traditional acid–base catalysts for lignin depolymerisation, a novel Ni/CaO–H-ZSM-5(60) catalyst was prepared to investigate the difficulty level of C–O bond of three model compounds cleavage in ethanol. It was observed that Ni/CaO–H-ZSM-5(60) had prominent performance on the C–O bond cleavage at very mild conditions (140 °C, 1 MPa H 2 ). Among them, the C–O bond of α- O -4 and β- O -4 could be completely cleaved within 60 min. Although the C–O bond of 4- O -5 had high bond energy, 41.2% of conversion was occurred in 60 min. The introduction of CaO could regulate the acidity of H-ZSM-5 to enhance the ability to break C–O bonds. Moreover, the possible pathways of C–O ether bonds in three lignin model compounds cleavage were proposed in order to selectively obtain target products from the raw lignin degradation.
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ADVANCED FUNCTIONAL MATERIALS
·
2022
·Vol. 32
·期 51
·2208676
·
IF 19.924
Bo Pang,Zuquan Jin,Yunsheng Zhang,Zhiyong Liu,Wei She,Penggang Wang,Yong Yu,Xiaoying Zhang,Chuansheng Xiong,Ning Li,Guowen Sun,Peng Zhao,Guojian Liu,Xiaoyun Song,Song Gao
Cement-based sensors (CBSs) have demonstrated potential in structural health monitoring (SHM) despite rare applications due to their poor flexibility and sensing accuracy/protection with robustness. Herein, a promising strategy is reported to design a waterborne epoxy resin (WEP)-modified cement-based composite coating sensorcapable of simultaneous stable SHM and durable protection. The interpenetrating network (IPN) formed by WEP within cement paste is bionic to the toughness and crack resistance of biological muscle tissue and balances the ion permeation performance and polarization of hydration products. The polymerization-redispersion progress and mechanism of calcium silicate hydrate (C-S-H) gel modified with [3-(2-aminoethylamino)-propyl]trimethoxysilane silsesquioxane (C-POSS) are characterized and revealed. The results show that the muscle-like IPN increases the cement-based coatings’ maximum deflection angle to 30° and improves the monitoring accuracy of compressive, tensile, and fatigue microchanges of concrete structures to more than 95%. The POSS···Ca 2+ ···C-S-H interaction in C-POSS partially transferred the intra-adhesive hydrogen bonds surrounding the nanoconducer into electrostatic bridging ones to maintain an excellent electromechanical conductive dispersion.
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Alexandria Engineering Journal
·
2024
·
IF 6.2
Hong Zhang,Ming Chen,Tiantian Liang,Zanpeng Zhang,Changhui Yang
The use of nanocarbon materials to enhance the toughness of fragile cementitious materials has attracted increasing attention for investigation. This study examines the effects of incorporating graphene oxide (GO) into NaOH-activated slag (AAS) pastes and mortars, focusing on workability, phase composition, mechanical properties, and the local mechanical properties of the interfacial transition zone (ITZ) between sand and paste. The experimental results indicate that the addition of GO decreases the flowability of NaOH-AAS pastes, with noticeable aggregation at concentrations above 0.03 wt%. Furthermore, GO enhances the hydration degree of ground granulated blast furnace slag (GGBS), leading to an increased amount of C-A-S-H gel without introducing new phases. In terms of macro performance, incorporating 0.03 wt% GO significantly improves the compressive and flexural strengths of NaOH-AAS mortars by 10.6 % and 17.9 %, respectively. Additionally, the presence of GO reduces the ITZ thickness from 30 to 15 micrometres in NaOH-AAS mortars, which likely contributes to the enhanced mechanical performance.
研究领域:
材料科学
·
水泥基材料
·
纳米复合材料
·
建筑材料化学
·
界面工程
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CHINESE JOURNAL OF CHEMISTRY
·
2013
·Vol. 31
·期 3
·371-376
·
IF 0.917
Wei Zhu,Haoyang Wang,Haihui Peng,Guosheng Liu,Yinlong Guo
Pd-catalyzed oxidative coupling reaction was of great importance in the aromatic C H activation and the formation of new C O and C C bonds. Sanford has pioneered practical, directed C H activation reactions employing Pd(OAc) 2 as catalyst since 2004. However, until now, the speculated reactive Pd(IV) transient intermediates in these reactions have not been isolated or directly detected from reaction solution. Electrospray ionization tandem mass spectrometry (ESI-MS/MS) was used to intercept and characterize the reactive Pd(IV) transient intermediates in the solutions of Pd(OAc) 2 -catalyzed oxidative coupling reactions. In this study, the Pd(IV) transient intermediates were detected from the solution of Pd(OAc) 2 -catalyzed oxidative coupling reactions by ESI-MS and the MS/MS of the intercepted Pd(IV) transient intermediate in reaction system was the same with the synthesized authentic Pd(IV) complex. Our ESI-MS(/MS) studies confirmed the presence of Pd(IV) reaction transient intermediates. Most interestingly, the MS/MS of Pd(IV) transient intermediates showed the reductive elimination reactivity to Pd(II) complexes with new C O bond formation into product in gas phase, which was consistent with the proposed reactivity of the Pd(IV) transient intermediates in solution.
研究领域:
有机化学
·
金属有机化学
·
分析化学
·
催化化学
·
质谱学
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危险品化学品经营许可证（带存储）