JOURNAL OF THE EUROPEAN CERAMIC SOCIETY
·
2023
·
IF 5.7
Mao Chen,Bingbing Fan,Haoyuan Lei,Zijie Song,Shaojun Zhang,Hailong Wang,Rui Zhang,Hongxia Li,Yongqiang Chen
Large size high density h-BN/ZrO 2 composites (ø = 110 mm, h = 15 mm) were rapidly prepared by spark plasma sintering (SPS) with sintering cycle 20 min. The effects of additives on the mechanical properties , microstructure evolution, and corrosion resistance of the h-BN/ZrO 2 composites were studied. The Al 2 O 3 , MgO , SiO 2 , La 2 O 3 and ZrO 2 rapidly formed heterogeneous eutectic crystals under the action of SPS. The low eutectic compounds significantly promoted the diffusion of h-BN or ZrO 2 , also increased the density. The flexural strength of h-BN/ZrO 2 composites could reach 196.31 MPa, and the apparent porosity was only 0.42 %. The additives are combined with zirconia to form a high viscosity eutectic, whose corrosion resistance to molten steel is obviously better than that of single ZrO 2 . The corrosion depth of h-BN/ZrO 2 composites was only 114 µm after corroded in molten steel at 1550 °C for 80 min. The comprehensive properties of h-BN/ZrO 2 composites were obviously improved by appropriate additives.
研究领域:
材料科学
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陶瓷工程
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产品关联
DOI
高影响因子
Surfaces and Interfaces
·
2025
·
IF 6.3
Ziqian Ding,Xiaolin Qiu,Huaxuan Liu,Lingli Gu
Functional form-stable phase change materials (FPCMs) offer great promise for thermal management in transport packaging due to their stability after phase change cycle and the extension of service life. However, challenges remain in enhancing thermal conductivity and energy storage efficiencies. In this study, a magnetically aligned h-BN-embedded superporous carbon foam-based FPCM containing paraffin (M-BN-CPCMs) was fabricated via a foam polymerization method followed by high-temperature carbonization. A super-porous hydrogel (SPH) precursor was used to construct a robust, highly porous carbon skeleton to accommodate more PCMs. To further enhance thermal conductivity, h-BN was functionalized with Fe 3 O 4 nanoparticles, and the resulting BN-Fe 3 O 4 was magnetically oriented within the carbon skeleton using a synchronous magnetization process. This novel design achieved a thermal conductivity improvement of over 90% compared to SPH. Additionally, the synergistic photothermal conversion effect achieved by the magnetic nanoparticles and carbon skeleton resulted in an outstanding photothermal conversion efficiency of approximately 90% for M-BN-CPCMs. Notably, the incorporation of BN-Fe 3 O 4 increased pore sizes, enabling higher paraffin loading capacity. The M-BN-CPCMs with large holes exhibit a remarkable phase change enthalpy of 154.9 J/g, demonstrating excellent energy storage capability, which surpasses that of superporous carbon foam skeleton-based FPCMs (CPCMs). The optimized M-BN-CPCMs demonstrated superior thermal energy storage, faster thermal charging rates, and improved thermal regulation, effectively reducing temperature fluctuations within insulated packaging. These findings underscore the potential of M-BN-CPCMs as a groundbreaking solution for energy storage and thermal management in transport packaging, addressing critical challenges in the field.
研究领域:
材料科学
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能源工程
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产品关联
DOI
高影响因子
JOURNAL OF ORGANIC CHEMISTRY
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2018
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IF 4.805
Chao Zhang,Yugang Song,Zhihui Sang,Lingpeng Zhan,Yu Rao
A strategy combining O- and N-containing directing groups has been developed for the synthesis of 2,2′-biaryl via Pd-mediated C–H bond activation and oxidative coupling. This new transformation may proceed through a mechanism involving Pd(II) and Pd(IV) intermediates. We found the use of PTSA and HFIP to be critical for the reaction and suggest that these reagents could serve as efficient ligands for this C–C bond formation. This methodology provides broad functional group tolerance, excellent reactivity, and high yields.
研究领域:
有机化学
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合成化学
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DOI
高影响因子
MATERIALS RESEARCH BULLETIN
·
2024
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IF 5.3
Yu Chang,Jianan Zhang,Ivan S. Babichuk,Hailong Liu,Yijie Liu,Jian Yang
The release of ammonia (NH 3 ) in industry or daily life is harmful to human health. A gas sensor was developed using h -MoO 3 nanorods and graphene film to detect and eliminate this. The h -MoO 3 nanorods were first synthesized by chemical bath deposition using ammonium molybdate tetrahydrate (NH 4 ) 6 Mo 7 O 24 •4H 2 O and HNO 3 and then deposited on the graphene film transferred to SiO 2 /Si substrate by electrochemical bubbling method. Subsequently, gas-sensitive h -MoO 3 @Graphene composite films were prepared and analyzed using Raman, XRD, SEM, and UV–vis. The gas sensor's performance was evaluated to detect NH 3 at a room temperature concentration range of 1–60 ppm. Compared with graphene, the conductivity of the composite film with 10 mg/ml h -MoO 3 nanorods was increased by 40 % and the sensitivity increased by 10 times. The sensor h -MoO 3 @G-10 showed the best sensing performance to 1 ppm NH 3 . Sensor sensitivity, response and recovery time are 1.1 %, 46.8 s and 17.8 s.
研究领域:
材料科学
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环境科学
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产品关联
DOI
高影响因子
Journal of Materials Chemistry A
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2024
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IF 10.7
Zhichao Ma,Chenyi Wang,Tianfang Yang,Gangya Wei,Jinrui Huang,Mengran Liu,Kun Zhang,Zunjie Zhang,Yang Liu,Shuyan Gao
Electrocatalytic nitrate (NO3−) reduction to ammonia (NH3) (NRA) is of great significance for solving the problem of urgent NO3− pollution in the environment and opening up a new route to synthesize NH3. However, NRA is limited by its multi-electron/proton transfer process and the NRA process relies heavily on atomic H* produced by H2O splitting, undergirding the necessity for effective NRA catalysts. Herein, three-dimensional (3D) porous phosphorus (P)-doped Cu–Ni alloy materials are constructed through a one-step electrodeposition synthesis. 3D porous materials modulate hydrophilicity and enrich active sites. The Cu d-band center can be tuned through Ni alloying to modify the adsorption energies of intermediates such as *NO3−, *NO2−, and *NH2. The hydrogenation evolution capacity of P promotes the hydrogenation process in the atomic H* path and effectively accelerates the NRA reaction rate. Density functional theory (DFT) calculations demonstrate that the charge transfer between the negatively charged Pδ− and the positively charged Niδ+ and Cuδ+ assists in generating more atomic H* for coupling with reaction intermediates, showing an enhanced catalytic activity at low overpotential. The optimal sample exhibits an exceptional NRA performance with an ammonia yield rate of 848.1 μmol h−1 cm−2 and a faradaic efficiency of 96.1%. This work provides a strategy for creating effective NRA catalysts through enhancing the atomic H* reduction strategy.
研究领域:
环境科学
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材料科学
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电催化
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产品关联
DOI
高影响因子
JOURNAL OF PHYSICAL ORGANIC CHEMISTRY
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2012
·Vol. 26
·期 1
·23-29
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IF 1.963
Chang-Di Chen,Wen-Bing Sheng,Guo-Jun Shi,Can-Cheng Guo
The regioselective hydroxylation of the aromatic C–H bond on a series of naphthalenes with different β-substituent R (R = H, Me, Et, i -Pr, OMe, COOH, Br, etc.) was studied, and the substituent effect on the regioselectivity was investigated. The electron-donating substituent afforded the aromatic C–H bond hydroxylation at the 1α position with more than 80% selectivity, while the electron-withdrawing substituent afforded the aromatic C–H bond hydroxylation at the 4α position with more than 60% selectivity of β-substituted naphthalene hydroxylated with metachloroperbenzoic acid catalyzed by tetrakis(pentafluorophenyl)porphyrin manganese(III) chloride. The research showed that the steric and electronic effects of the substituent appeared to play a significant role in determining the regioselectivity, and the electronic effect was of more importance than the steric effect of the substituent in the current situation. The studies may provide additional proofs for the stepwise mechanism of the aromatic C–H bond hydroxylation through a cationic intermediate. Copyright © 2012 John Wiley & Sons, Ltd.
研究领域:
有机化学
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催化化学
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产品关联
DOI
高影响因子
ORGANIC & BIOMOLECULAR CHEMISTRY
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2014
·Vol. 12
·期 18
·2969-2978
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IF 3.487
Jiajun Zhang,Pinhua Li,Lei Wang
A novel KOAc-promoted α-position C–H activation and alkynylation of ethers with alkynyl bromides to 2-alkynyl ethers has been developed under transition-metal-free and simple reaction conditions. In addition, this methodology can also be extended to the vinylation of ethers with vinyl bromides in excellent regio- and stereo-selectivity. A wide range of direct C(sp)–C(sp3) and C(sp2)–C(sp3) bonds has been formed through this protocol, which offers a new and alternative route.
研究领域:
有机化学
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合成化学
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产品关联
DOI
PubMed
高影响因子
ORGANIC & BIOMOLECULAR CHEMISTRY
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2014
·Vol. 12
·期 21
·3493-3498
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IF 3.487
Yaping Zhao,Lu Sun,Tieqiang Zeng,Jiayi Wang,Yanqing Peng,Gonghua Song
Copper-catalyzed direct olefination of benzaldehydes into 1,3-diarylpropenes by a novel domino Knoevenagel-decarboxylation-Csp3-H activation sequence is reported. This method provides a concise and effective route toward the synthesis of unsymmetrical 1,3-diarylpropene derivatives.
研究领域:
有机化学
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催化化学
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产品关联
DOI
PubMed
高影响因子
ACS Applied Materials & Interfaces
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2023
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IF 9.5
Ying Zhang,Bin Wei,Hao Liang
An organometallic complex-catalyzed artificial coenzyme regeneration system has attracted widespread attention. However, the combined use of organometallic complex catalysts and natural enzymes easily results in mutual inactivation. Herein, we establish a rhodium-based metal–organic framework (MOF)-on-MOF difunctional core–shell nanoreactor as an artificial enzymatic NAD(P)H regeneration system. UiO67 as the core is used to capture rhodium molecules for catalyzing NAD(P)H regeneration. UiO66 as the shell is used to specifically immobilize His-tagged lactate dehydrogenase (LDH) and serve as a protection shield for LDH and [Cp*Rh(bpy)Cl]+ to prevent mutual inactivation. A variety of results indicate that UiO67@Rh@UiO66 has good activity in realizing NAD(P)H regeneration. Noteworthily, UiO67@Rh@UiO66@LDH maintains a high activity level even after 10 cycles. This work reports a novel NAD(P)H regeneration platform to open up a new avenue for constructing chemoenzyme coupling systems.
研究领域:
生物化学
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材料科学
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酶工程
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产品关联
DOI
PubMed
高影响因子
ANALYTICAL CHEMISTRY
·
2023
·
IF 7.4
Jingjing Zhang,Fenglian Guo,Jingfeng Zhu,Zhimei He,Lin Hao,Lixing Weng,Lianhui Wang,Jie Chao
The development of noninvasive and sensitive detection methods for the early diagnosis and monitoring of bladder cancer is critical but challenging. Herein, an ultrasensitive electrochemiluminescence (ECL) immunosensor that uses Ru(bpy)32+–metal–organic framework (Ru-MOF) nanospheres and a DNA tetrahedral (TDN) probe was established for bladder cancer marker complement factor H-related protein (CFHR1) detection. The synthesized Ru(bpy)32+–metal–organic frameworks (Ru-MOFs) served as a linked substrate for immobilization of AuNPs and antibody (Ab2) to prepare the ECL signal probe (Ru-MOF@AuNPs-Ab2), exhibiting a stable and strengthened ECL emission. At the same time, the inherent advantages of TDN probes on the electrode as the capture probe (TDN-Ab1) improve the accessibility of targets to probes. In the presence of CFHR1, the signal probe Ru-MOF@AuNPs-Ab2 was modified on the electrode through immune binding, thereby obtaining an outstanding ECL signal. As expected, the developed ECL immunosensor exhibited splendid performance for CFHR1 detection in the range of 0.1 fg/mL to 10 pg/mL with a quite low detection limit of 0.069 fg/mL. By using the proposed strategy to detect CFHR1 from urine, it showed acceptable accuracy, which can effectively distinguish between bladder cancer patients and healthy samples. This work contributes to a novel, noninvasive, and accurate method for early clinical diagnosis of bladder cancer.
研究领域:
生物医学工程
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肿瘤学
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分析化学
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产品关联
DOI
PubMed
高影响因子
KOREAN JOURNAL OF CHEMICAL ENGINEERING
·
2020
·Vol. 37
·期 6
·961-968
·
IF 2.69
Dai Ping,Sun Xiaowei,Xu Dongyan,Tan Feng
Alumina supported bimetallic cobalt-iron oxide (Co 3 O 4 -Fe 2 O 3 /Al 2 O 3 ) catalyst was prepared via co-impregnation of boehmite with the mixture solution of cobalt nitrate and iron nitrate followed by calcination in air. X-ray photoelectron spectroscopy and high-resolution transmission electron microscope analyses confirmed the existence of highly dispersed Co 3 O 4 and Fe 2 O 3 nanoparticles in the as-prepared catalysts. The catalytic activity of Co 3 O 4 -Fe 2 O 3 /Al 2 O 3 was evaluated for the degradation of H-acid in aqueous solution by heterogeneous activation of peroxymonosulfate. The results indicated that the Co 3 O 4 -Fe 2 O 3 /Al 2 O 3 catalyst exhibited an identical initial activity but much better recyclability than Co 3 O 4 /Al 2 O 3 due to its low amount of metal leaching and possible redox circle of Co(II)/Co(III). Electron paramagnetic resonance spectroscopy and radical quenching experiments suggested that singlet oxygen ( 1 O 2 ) contributed much more than ·OH and SO 4 • to H-acid degradation, and the degradation mainly followed a nonradical reaction mechanism.
研究领域:
环境科学
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催化化学
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DOI
高影响因子
CATALYSIS TODAY
·
2022
·
IF 6.562
Xinyi Xing,Ying Guan,Liping Zhang,Xian Shi,Han Wu,Hui Gao,Siquan Xu
A catalytic system that is both efficient and recyclable is desirable for production 5-hydroxymethylfurfural (HMF) from glucose. In this study, the catalytic system composed of H 2 O (NaCl) -tetrahydrofuran (THF) biphasic system and H-β zeolite was found to have excellent performance for the glucose conversion into HMF. The physicochemical properties of the H-β zeolite catalyst, the dosage of the system components, and the reaction parameters were investigated in detail to optimize the production efficiency of HMF. Under optimal reaction conditions, an advanced level of 84% HMF yield was obtained from glucose. After the reaction was completed, all components of the catalytic system can be recovered, realizing no waste of reagents. Moreover, the recycled H-β(30) zeolite catalyst maintained considerable catalytic stability after five consecutive cycles. Therefore, it is reasonable to believe that the efficient, inexpensive, and recyclable H 2 O (NaCl) -THF catalytic system containing H-β(30) zeolite is capable of showing promising application potential in the future.
研究领域:
催化化学
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可再生资源转化
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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）