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81.
B. Shankar Goud Y. Dharmendar Reddy S.R. Mishra M. Ijaz Khan Kamel Guedri Ahmed M. Galal 《印度化学会志》2022,99(8):100618
For this research, an examination on the magnetohydrodynamic flow of a micropolar fluid across a moving vertical porous plate for the presence of thermal radiation is achieved. It is necessary to translate the partial differential equations regulating the flow, heat, & mass transfer into dimensionless form employing proper non-dimensional variables, which are then cracked numerically by utilizing the Finite difference approach. Graphs are used to represent numerical values of various flow profiles; however, tables are used to represent the simulated values of rate coefficients. The velocity rises when the value of Grashof number, dimensionless viscosity ratio is raised, and the opposite effect is seen when the value of magnetic parameter, micro-gyration factor is raised. The result in skin friction coefficient improves when the values of magnetic parameter, micro-gyration factor, Prandtl number, and radiation are raised higher. 相似文献
82.
电催化二氧化碳还原反应(E-CO2RR)可在温和条件下将CO2转化成高附加值燃料或化学品,近年来受到广泛关注,其在实际反应中涉及到气体扩散和多电子转移等复杂过程,构筑高效、稳定的催化电极是其发展的核心之一。然而,传统涂敷电极制备时,需要将催化剂与粘结剂混合涂覆于集流体表面,此过程会造成活性位点包埋和传质过程受限,致使催化剂活性位利用率下降,同时在反应过程中电极表面容易粉化,造成稳定性下降,难以重复利用。因此,如何调控电极反应界面,提升催化剂活性位的利用率仍面临挑战。将催化剂原位生长于集流体上得到的一体化电极可直接应用于电催化反应,不仅有利于提升活性位利用率以及电荷传输能力,还能有效调控三相界面处的微观反应环境(如pH、反应物及反应中间体的浓度等),从而实现电催化性能强化。本文综述了一体化电极用于E-CO2RR的最新进展,分析了结构和表界面调控对E-CO2RR性能的影响规律,并对该领域仍然存在的挑战和未来一体化E-CO2RR电极的发展进行了评述与展望。 相似文献
83.
YANG Zhichen KANG Xiaoting ZOU Bo YUAN Xuna LI Yajie WU Qin GUO Yupeng 《高等学校化学研究》2022,38(4):1065-1072
The massive discharge of biomass wastes not only causes waste of resources, but also pollutes the environment. Therefore, converting biomass wastes into carbon materials is an effective way to solve the above problems. Here, using biomass waste pig nails as raw materials and K2CO3 as chemical activators, the N-doped porous carbon(KPNC) is prepared by direct pyrolysis. As an electrode for supercapacitors, the electrochemical tests of KPNCs showed that they exhibited good electrochemical performance and excellent cycling stability. When the current density is 0.2 A/g, the specific capacitance is up to 344.6 F/g. Moreover, it still maintains 97.6% initial capacitance retention after 2000 cycles at a high current density of 5 A/g. Above exceptional electrochemical performances may be ascribed to an appropriate porous structure(Smicro/Stotal=80.31%, Vmicro/Vtotal=76.19%), high nitrogen contents(4.44%, atomic fraction), oxygen contents(9.13%, atomic fraction) as well as small internal resistance. The above experimental results show that the conversion of pig nails to porous carbon can reduce the waste of resources and alleviate environmental pollution. 相似文献
84.
《Arabian Journal of Chemistry》2022,15(9):104031
Quercus mongolica leaf (QL), an easily available biomass, was used as the precursor for preparing the hierarchical porous carbon with a large specific surface area and high adsorption capacities toward the representative dye and antibiotic. After being carbonized, QL was further chemically activated, and potassium hydroxide was proved to be a better activator than sodium hydroxide. The QL-derived porous carbon (PCQL) exhibited abundant micro- and mesopores, and the specific surface area reached 3275 m2 g?1. The performances of PCQL were evaluated through adsorbing rhodamine B (RhB) and tetracycline hydrochloride (TC) from water. Four adsorption isotherm models (the Langmuir, Freundlich, Sips, and Redlich-Peterson models), three adsorption kinetic models (the pseudo-first-order, pseudo-second-order, and intra-particle diffusion models), and the thermodynamic equations were used to investigate the adsorption processes. The pseudo-second-order kinetic model and the Sips isotherm model fitted the experimental data well, which indicates that the adsorption processes were controlled by the amount of adsorption active sites on the surface of PCQL, and these adsorption active sites had different affinities for the adsorbates. The maximum adsorption capacities of PCQL toward RhB and TC were 1946.0 and 1479.6 mg g?1, respectively, based on the Sips model. The thermodynamic analysis indicates that the adsorption of PCQL toward adsorbents was spontaneous physical processes accompanied by the increasing disorder degree. The adsorption mechanism was attributed to the combination of the pore-filling, hydrogen bond, and π-π interactions. Moreover, in the fixed-bed experiments, the Yoon-Nelson model fitted the breakthrough curves well, and about 8 L wastewater containing RhB (200 mg L?1) may be effectively treated by 1.0 g of PCQL. Above results indicate that QL is a promising precursor for preparing functional porous carbon materials. 相似文献
85.
X.-T. Mu Y.-S. Ouyang L.-M. Pei Z.-X. Peng S.-Q. Shao S.-M. Wang H. Xiong Y. Xiao Q.-Y. Yang 《Materials Today Chemistry》2022
Adsorptive separation of C2H6 from C2H4 by adsorbents is an energy-efficient and promising method to boost the polymer grades C2H4 production. However, that C2H6 and C2H4 display very similar physical properties, making their separation extremely challenging. In this work, by regulating the pore environment in a family of chitosan-based carbon materials (C-CTS-1, C-CTS-2, C-CTS-4, and C-CTS-6)- we target ultrahigh C2H6 uptake and C2H6/C2H4 separation, which exceeds most benchmark carbon materials. Explicitly, the C2H6 uptake of C-CTS-2 (166 cm3/g at 100 kPa and 298 K) has the second-highest adsorption capacity among all the porous materials. In addition, C-CTS-2 gives C2H6/C2H4 selectivity of 1.75 toward a 1:15 mixture of C2H6/C2H4. Notably, the adsorption enthalpies for C2H6 in C-CTS-2 are low (21.3 kJ/mol), which will facilitate regeneration in mild conditions. Furthermore, C2H6/C2H4 separation performance was confirmed by binary breakthrough experiments. Under different ethane/ethylene ratios, C-CTS-X extracts a low ethane concentration from an ethane/ethylene mixture and produces high-purity C2H4 in one step. Spectroscopic measurement and diffraction analysis provide critical insight into the adsorption/separation mechanism. The nitrogen functional groups on the surface play a vital role in improving C2H6/C2H4 selectivity, and the adsorption capacities depend on the pore size and micropore volume. Moreover, these robust porous materials exhibit outstanding stability (up to 800 °C) and can be easily prepared on a large scale (kg) at a low cost (~$26 per kg), which is very significant for potential industrial applications. 相似文献
86.
R. Shanmugam J. Ganesamurthi T.-W. Chen S.-M. Chen M. Balamurugan M.A. Ali A.M. Al-Mohaimeed W.A. Al-onazi K. Alagumalai 《Materials Today Chemistry》2022
Herein, we reported the fabrication of porous iron oxide/carbon black (P–Fe2O3/CB) composite through a two-step engineering method. At first, Prussian blue microcubes were used as a precursor and further calcined to form P–Fe2O3 microcubes. The intercalation of CB nanoparticles with P–Fe2O3 nanocubes was processed through the ultrasonication method. The obtained P–Fe2O3/CB were successfully scrutinized through various physiochemical characterization methods. The proposed P–Fe2O3/CB-modified glassy carbon electrode sensor was successfully implemented in the electrochemical sensing of chlorpromazine hydrochloride due to its very low charge transfer resistance (Rct) compared to the other electrode modifiers. The sensitive detection of CPMH through differential pulse voltammetry exemplifies an excellent electroanalytical performance such as a wide linear range of 0.5–1472 μM, a lower detection limit (0.001 μM), and an appraisable sensitivity of 1.99 μA/μM cm?2 due to its availability of a high number of active sites and its large surface area, respectively. It also expresses excellent selectivity, repeatability, reproducibility, and stability results. Moreover, the practical feasibility of the as-fabricated P–Fe2O3/CB/glassy carbon electrode sensor shows exquisite recovery (98.1–100.8%) results with an appraisable current response in various biological, pharmaceutical, and environmental samples. 相似文献
87.
Huijun Wang Jie Gao Dr. Xiang Xu Dr. Baogen Liu Lingyun Yu Yadong Ren Dr. Rui Shi Prof. Zheng Zeng Prof. Liqing Li 《化学:亚洲杂志》2021,16(9):1118-1129
To investigate the effects of oxygen-containing functional groups on the adsorption of volatile organic compounds (VOCs) with different polarity, oxygen-rich porous carbon materials (OPCs) were synthesized by heat treatment of glucose/potassium oxalate material. The carbon material had a large specific surface area (1697 m2 g−1) and a high oxygen content (18.95 at.%). OPC exhibited high adsorption capacity of toluene (309 mg g−1) and methanol (447 mg g−1). The specific surface area and total pore volume determined the adsorption capacity of toluene and methanol at the high-pressure range, while the oxygen-containing groups became the main factor affecting the methanol adsorption at the low-pressure range due to the hydrogen bond interaction through the density functional theory (DFT) calculations. This study provides an important hint for developing a novel O-doped adsorbent for the VOCs adsorption applications and analyzing the role of oxygen-containing groups in the VOCs adsorption under the low-pressure range. 相似文献
88.
Venkatachalam Rajagopal Nivedhitha Jothi Narayanan Murugavel Kathiresan Deepak Kumar Pattanayak Vembu Suryanarayanan 《Materials Today Chemistry》2021
Herein, we report the synthesis of new covalent organic polymer comprising triazine and o-tolidine by solvothermal method. The formation of polymer was confirmed by Fourier transform infra red spectroscopy (FT-IR), cross polarization–magic angle spinning nuclear magnetic resonance (NMR), transmission electron microscopy, and scanning electron microscopy. Their antibacterial activity toward S. aureus (gram-positive) and P. aeruginosa (gram-negative) was assessed by the optical density measurements and direct contact method. These results have great significance toward the design of new porous polymers for antibacterial applications. 相似文献
89.
In the present work, the influence of porosity and boron on shear thickening behavior of hybrid mesoporous silica has been studied. Three different levels of boron modification were performed by varying the molar composition of boric acid viz., 1.5 mmol, 2.5 mmol, and 3.5 mmol in a co-condensation approach. The incorporation of boron in mesoporous silica network was confirmed by various techniques such as Fourier transform infra-red (FTIR), and 11B solid- state nuclear magnetic resonance (NMR) spectroscopy. The morphology and particle size were confirmed by using scanning and transmission electron microscopy. To evaluate the effect of boron and porosity on the shear thickening behavior, dispersions were prepared from mesoporous boron- modified silica (MSiB), control mesoporous silica (MSi), non-porous boron-modified silica (SiB), and control non-porous silica (Si) in polyethylene glycol. The shear thickening behavior was studied using steady shear rheology. The dispersion prepared from different loadings of synthesized MSiB containing 1.5 mmol boron showed more than 16 times increase in viscosity (657.7 Pa.s) compared to that of MSi (39.2 Pa.s) at a fairly low volume fraction (φ = 0.15) of silica. It is expected that the highly ordered mesoporous architecture of hybrid silica has improved the interaction between the particle and the dispersing medium through hydrogen bonding. The porous morphology of the hybrid mesoporous silica as well as the incorporation of boron in the silica network favors the formation of a frictional contact network, and a transition from continuous shear thickening (CST) to discontinuous shear thickening (DST) behavior was observed. Therefore, silica prepared via incorporation of boron as well as porosity can be material of interest in variety of applications, for example, soft body armors, sporting goods, and shear thickening electrolytes for high impact resistant batteries. 相似文献
90.
《Journal of Saudi Chemical Society》2021,25(9):101317
The novel palladium nanoparticles (Pd@POPs) were successfully prepared with controllable sizes and dispersity through the introduction of H2PdCl4 into urea-linked porous organic polymers (POPs) in an aqueous environment followed by reducing Pd(II) to Pd(0) by NaBH4. The newly prepared Pd@POPs were thoroughly characterized by FT-IR, ICP-AES, BET, XRD, SEM and TEM. Furthermore, the catalytic reactivities of this novel Pd@POPs were investigated via Heck, Suzuki-Miyaura cross-coupling reaction and nitroarene reduction, and they exhibited superior catalytic performances in all these three reactions, producing the corresponding products in up to quantitative yields. Additionally, the Pd@POPs had excellent recyclability in both Heck and Suzuki-Miyaura cross-coupling reactions with the repeating time up to four times and ten times, respectively, along with no obvious decrease of catalytic reactivities. 相似文献