Journal of Physical Chemistry C
·
2021
·
IF 4.126
Jian He,Huining Zhao,Xinru Hu,Zhiyong Fang,Jilin Wang,Rui Zhang,Guoyuan Zheng,Bing Zhou,Fei Long
In this study, a new type of 0-dimensional organic–inorganic hybrid perovskite single crystal (2-5-py)2MnBr4 was synthesized using 2-amino-5-methylpyridine (2-5-py) as the organic ligand. The crystal is a center-symmetric P-1 space group with a grain size of 20 mm, which belongs to the triclinic crystal system. It has a strong absorption of violet and blue light as well as excellent thermal stability. Its optical band gap is 2.38 eV, which is in good agreement with the theoretical band gap (2.39 eV) calculated by density functional theory. Under the excitation of a suitable light source, it can emit 526 nm pure bright green lights, which are confirmed by the main peaks to be almost in the green range with a full width at half maximum of 45 nm. As a result, the quantum efficiency and fluorescence lifetime reached a high level of 44.2% and 117 μs, respectively. Based on the good fluorescence performance of the crystal, a white LED with a color rendering index of 97 was finally successfully fabricated, realizing the leap from basic materials to optoelectronic devices.
研究领域:
材料科学
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光电材料
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晶体结构研究
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产品关联
DOI
高影响因子
JOURNAL OF COORDINATION CHEMISTRY
·
2019
·
IF 1.685
Yafang Ge,Guoting Li,Dongxia Fu,Lina Liu,Benlai Wu
Two metal–organic frameworks based on a multifunctional ligand 2-(5-bromo-pyridin-3-yl)-1H-imidazole-4,5-dicarboxylic acid (H3L), [Mn(HL)(C2H5OH)]n (1) and {[Zn(HL)(H2O)2]·H2O}n (2), have been hydro/solvothermally synthesized and characterized by IR, elemental analyses, X-ray powder and single-crystal diffractions, and thermogravimetric analyses. In 1, (HL)2– ligands adopt the μ
3-kN,O:kN′,O′:kN′′ coordination mode and use their imidazoledicarboxylates to bis-chelate MnII into left- and right-handed helixes which are further bridged into a mesolayer structure with (4·82) topology through the coordination of their pyridyl groups. In 2, (HL)2– ligands only use their imidazoledicarboxylates to bis-chelate ZnII into linear chains which are further linked into a 2D supramolecular framework through interchain hydrogen–bonding interactions. Interestingly, the structures of 1 and 2 are mainly dominated by the bis-N,O-chelation of the imidazoledicarboxylate in (HL)2–. As for the formation of the imidazoledicarboxylate-bridged helical chains in 1 or straight chains in 2, it largely depends on the cis- or trans-chelation of two imidazoledicarboxylates around the same metal center. Magnetostructural analysis of 1 discloses that the bis-N,O-chelating imidazoledicarboxylate of (HL)2– transmits antiferromagnetic interactions along the imidazoledicarboxylate-bridged helical chain with the spin-coupling constant of –0.71 cm–1. Additionally, 2 emits greatly enhanced blue fluorescence mainly originating from the intraligand charge transition.
研究领域:
材料科学
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化学
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配位化学
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晶体工程
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产品关联
DOI
高影响因子
JOURNAL OF MOLECULAR LIQUIDS
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2022
·
IF 6.633
Mansoor Khan,Ozgur Ozalp,Muslim Khan,Mustafa Soylak
In this work, we report the preparation of Fe 3 O 4 -Ti 3 AlC 2 max phase impregnated with 2-(5-Bromo-2-pyridylazo-5-(diethylamino) phenol) and its implementation for the extraction of cadmium, lead and cobalt from water and food samples. Blended Fe 3 O 4 -Ti 3 AlC 2 max phase impregnated with 2-(5-Bromo-2-pyridylazo-5-(diethylamino) phenol) was characterized using different instrumental techniques like scanning electron microscopy (SEM), surface area analyser (SAA), energy dispersive X-rays (EDX), Fourier transform infrared spectroscopy (FT-IR) and X-rays diffraction (XRD) for surface morphology, surface region, elemental composition, functional group and crystallinity, respectively. Factors that impact the % recoveries of analyte i.e pH, sample volume, vortex time, desorption condition and matrix impact were optimized. Analytical parameters like limit of detection (LOD) (Cd: 0.093 µg/L, Pb: 0.297 µg/L, Co: 0.223 µg/L), limit of quantifications (LOQ) (Cd: 0.310 µg/L, Pb: 0.992 µg/L, Co: 0.744 µg/L) preconcentration factors (PF) (Cd = Pb = Co: 40), enrichment factors (EF) (Cd: 39.8, Pb: 39, Co: 40) and relative standard deviation (RSD) (Cd: 3.8, Pb: 5.98, Co: 4.0) were determined under optimized trial conditions. The proposed strategy was tested using certified reference materials like TMDA-64.3 natural water and tobacco leaves (INCT-OBTL-5) for trace metal analysis. The developed strategy was also applied effectively to natural water samples and food samples using the standard addition method with good recovery results.
研究领域:
分析化学
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环境科学
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DOI
高影响因子
FUEL
·
2021
·
IF 6.609
Bo Wang,Ya-Feng Huang,Peng-Fei Wang,Xiao-Jie Liu,Chang Yu,Wei-Guang Li,Xiao-Feng Wang,Xiong-Min Liu
The thermal oxidation reaction of 2,5-dimethylfuran (DMF) was investigated using a custom-designed mini closed pressure vessel test (MCPVT) and traced by 1 H nuclear magnetic resonance( 1 H NMR). The oxidation behavior was monitored by-via temperature–time (T-t) and pressure–time (p-t) plots of MCPVT recording. Oxidation products were determined via gas chromatography-mass spectrometry (GC–MS), and the generated peroxide was examined by iodimetry and thin-layer chromatography (TLC), with the thermal decomposition hazard evaluation by differential scanning calorimeter (DSC) and MCPVT. Results show that the DMF oxidation reaction proceeded through initial oxygen absorption at 39.3 °C, followed by an exothermic self-accelerating oxidation at 84.5 °C. DMF could form high level peroxide in auto-oxidation; the decomposition of peroxides would lead to the radical oxidation that the generated ·OH radical mainly attacks on the position 2/5 of DMF with subsequent addition of O 2 initiating ring-opening reaction, in which DMF was firstly converted to cis -3-hexene-2,5-dione, and then produced the trans -3-hexene-2,5-dione with strong photoisomerism. DMF oxidation showed a high level of residue formation, and those solid products contained considerable amount of peroxides with a high thermal hazard; its exothermic onset temperature (T 0 ) and decomposition heat (Q DSC ) of 58.8 °C and 1982.3 J∙g −1 , and the decomposition maximum temperature rising rate (dT/dt) max and maximum of pressure rising rate (dp/dt) max was 9.98 °C∙s −1 and 291 kPa∙s −1 , respectively. Thermal decomposition of those peroxide products could give rise to thermal runaway of DMF oxidation, and further transformed into a detonation possibly.
研究领域:
化学工程
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安全科学
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产品关联
DOI
高影响因子
Journal of Energy Chemistry
·
2015
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IF 2.352
Xianxiang Liu,Hui Ding,Qiong Xu,Wenzhou Zhong,Dulin Yin,Shengpei Su
A mild and simple process for the effective oxidation of 5-hydroxymethylfurfural (HMF) into 2,5-diformylfuran (DFF) has been developed using NaNO 2 as the oxidant. Some important reaction parameters were investigated to optimize the oxidation of HMF into DFF. It was found that the reaction solvent was very crucial for this reaction. Trifluoroacetic acid was the best solvent for the oxidation of HMF into DFF by NaNO 2 . Under the optimal reaction condition, almost quantitative HMF conversion and high DFF yield of 90.4% were obtained after 1 h at room temperature.
研究领域:
化学工程
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有机化学
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催化
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产品关联
DOI
高影响因子
POLYMER DEGRADATION AND STABILITY
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2015
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IF 3.163
Hongli Wu,Binbin Wen,Hua Zhou,Jiadong Zhou,Zuolong Yu,Liyan Cui,Ting Huang,Fei Cao
Polyethylene 2, 5-furandicarboxylate-lactic acid copolyesters (PEFL) were synthesized from bis (hydroxyethyl)-2, 5-furandicarboxylate and oligomer of l -lactic acid, through two-stage condensation . The polyesters were characterized using FTIR, 1 H NMR, GPC , and WXRD. The weight-average molecular weight (M w ) of the polyesters ranged from 68240 to 130433. The glass transition temperature (T g ) of the copolyesters increased gradually with increasing content of 2, 5-furandicarboxylate. In phosphate buffer solution (PBS, pH = 7.4) and in soil, the degradability of the polyesters was evaluated for 55 d. More weight loss was obtained with a higher ratio of lactate polymers in soil than those with a lower ratio in PBS. After 55 d, the weight loss of PEFL20/80 reached 65% and 24% in soil and PBS, respectively. However, the mole fraction of lactyl and furanic units that was calculated by 1 H NMR data did not change. Comparing the scanning electron microscopy images, we found many micro-cracks on the copolyester surfaces. Meanwhile, M w and T g also decreased prominently during degradation.
研究领域:
材料科学
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环境科学
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生物化学
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产品关联
DOI
高影响因子
CHEMICAL ENGINEERING SCIENCE
·
2021
·
IF 4.311
Gaobo Lin,Wenwen Lin,Jianghua Wu,You Zhan,Francis Okejiri,Mingwei Weng,Jie Fu
Biomass-derived 2,5-furandicarboxylic acid (FDCA) is considered a viable alternative to petroleum-derived terephthalic acid as a monomer in the production of bioplastic. FDCA is currently mainly produced via a two-step process involving the conversion of fructose to 5-hydroxymethylfurfural (HMF) and the subsequent oxidation of HMF to FDCA. However, the storage stability HMF is far below the industrial expectations, further inhibiting the HMF-mediated route. Herein, we report efficient oxidation of 5-methoxymethylfurfural (MMF) to FDCA over a homemade Ru/hydroxyapatite (Ru/HAP) catalyst. A complete conversion of MMF and > 65% molar yield of FDCA could be realized under mild reaction conditions of 130 °C and 1 MPa O 2 pressure. The effects of process parameters, including MMF/catalyst ratios, reaction temperature/time, and O 2 pressure, were systematically studied and optimized on MMF oxidation. A plausible reaction pathway was also proposed. This study and our previously reported fructose-to-MMF work may provide a feasible MMF-intermediated route for large-scale industrial FDCA production.
研究领域:
化学工程
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可再生资源
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催化化学
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产品关联
DOI
高影响因子
CATALYSIS LETTERS
·
2022
·Vol. 152
·期 12
·3716-3724
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IF 2.936
Chen Hong,Li Yingying,Yu Linhao,Wang Sen,Ma Xueli,Wang Can,Li Yongdan
A series of hydroxyapatite (HAP) supports with different Ca/P ratios were synthesized to prepare the MnO x /HAP catalysts. A MnO x /HAP catalyst showed highly efficient conversion of 5-hydroxymethylfurfural (HMF) into 2, 5-diformylfuran (DFF) in toluene solvent under no-alkali condition. 86.4% conversion of HMF with 90.9% selectivity of DFF at 120 °C for 12 h under 1.0 MPa O 2 over the MnO x /HAP-10.0-400 were obtained. The redox of Mn 4+ /Mn 3+ improved the oxidation of 5-HMF to DFF by the lattice oxygen, and the lattice oxygen was replenished by adsorbing O 2 molecules. The reusability tests were found the catalyst could be reused up to four cycles without notable loss of catalytic activity. The MnO x /HAP-10.0-400 was a stable and reusable material for further industrial exploration of DFF in an environmentally friendly way. Graphical Abstract
研究领域:
化学工程
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催化材料
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绿色化学
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产品关联
DOI
高影响因子
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
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2019
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IF 4.978
Ting Wang,Junnan Wei,Huai Liu,Yunchao Feng,Xing Tang,Xianhai Zeng,Yong Sun,Tingzhou Lei,Lu Lin
2, 5-Bishydroxymethylfuran (BHMF) has been currently emerged as a promising biomass-derived monomer . It is highly desirable to proceed a chemical process at a high substrate concentration, by which a facile and cost-effective separation of products can be expected. Herein, we report for the first time on the hydrogenation of highly concentrated 5-hydroxymethylfurfural (HMF) in deep eutectic solvents (DESs), giving a near quantitative selectivity towards BHMF in ChCl-glycerol DES at 25 °C in 3 h using NaBH 4 as the H-donor. DES is hailed as a new class of green solvent, in which HMF/BHMF could be stabilized by the strong hydrogen-bond interaction, and allowed the selective hydrogenation of HMF at high concentration up to 40 wt%. Notably, the resulting BHMF could be facilely separated by extraction with ethyl acetate, and then high purity of BHMF with a desirable isolated yield around 80% was obtained after removing of ethyl acetate. Additionally, the reaction efficiency of HMF hydrogenation in DESs was verified to be strongly associated with the viscosity of DESs and the p K a value of hydrogen-bonding donor.
研究领域:
化学工程
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绿色化学
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生物质转化
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DOI
高影响因子
KOREAN JOURNAL OF CHEMICAL ENGINEERING
·
2020
·Vol. 37
·期 2
·224-230
·
IF 2.69
Si Zhihao,Zhang Xin,Zuo Miao,Wang Tao,Sun Yong,Tang Xing,Zeng Xianhai,Lin Lu
2, 5-furandicarboxylic acid (FDCA) is a one of the most promising biomass-derived chemicals to substitute the non-renewable terephthalic acid as the monomer for producing polyethyleneterephthalate. At present, the oxidation of HMF is regarded as a prevalent way to prepare FDCA. Nevertheless, the isolation and storage of HMF is still a challenge. Herein, based on the higher stability of 5-formyloxymethylfurfural (FMF) than 5-hydroxymethylfurfural (HMF), we present an effective preparation route to prepare FDCA by substituting HMF with FMF as feedstock. A complete conversion of FMF and a 93.55% selectivity of FDCA were obtained in the mixed solvent of water and 1, 2-dioxane using Ru/C as catalyst and O 2 as oxidant. An improved process was developed for preparing FDCA using FMF as feedstock. The investigation of conversion pathway showed that FMF and HMF were simultaneously oxidized to 2, 5-diformylfuran (DFF) in a case of the existence of the reversible equilibrium between FMF and HMF. Then DFF was oxidized to 5-formyl-2-furancarboxylic acid (FFCA). Subsequently, FFCA was oxidized to FDCA. In this process, the oxidation of FFCA to FDCA was determined as the rate-determining step. Furthermore, appropriate alkalinity favored the selectivity of FDCA and the conversion of FMF.
研究领域:
化学工程
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生物质化学
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催化化学
✓ 已验证
产品关联
DOI
高影响因子
APPLIED CLAY SCIENCE
·
2023
·
IF 5.6
Xuemin Zhong,Peng Yuan,Samahe Sadjadi,Dong Liu,Yanfu Wei
The oxidation of 5-hydroxymethylfurfural (HMF) to 2, 5-diformylfuran (DFF) is an important reaction for the conversion of renewable biomass into feedstock chemicals. In this work, palygorskite (Pal)-supported ruthenium (Ru) catalysts were developed for the efficient selective oxidation of HMF to DFF. Using natural clay mineral palygorskite as the support enabled the immobilization and dispersion of Ru nanoparticles . A 100% HMF conversion, 98% DFF yield, and 98% DFF selectivity were obtained over Ru(III)/Pal catalyst after 4.5 h under the optimal reaction conditions at 110 °C and 10 bar of O 2 in toluene. Ru nanoparticles and palygorskite synergistically achieve the excellent catalytic performance of the catalyst. The Ru metal active sites facilitate the activation of the reactants or intermediates, accelerating the formation of DFF. Furthermore, due to their different particle sizes and Ru species, the Ru(III)/Pal catalyst exhibits higher catalytic activity than the Ru(0)/Pal catalyst for the oxidation of HMF to DFF. The palygorskite-enhanced dispersion effect on Ru nanoparticles augments the catalytic activity. Moreover, the palygorskite-supported Ru catalyst showed good stability and was reused for at least five times consecutive cycles without significant loss of its catalytic activity.
研究领域:
催化
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化学工程
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL PHYSICS LETTERS
·
2024
·
IF 2.8
Xu Gao,Aihu Feng,Le Mi,Yang Yu,Yun Yu
Adsorption is one of the most effective methods for controlling the concentration of VOCs pollution. In this work, the hierarchical NaY zeolites with size-controlled mesopores in the range of 2–5 nm are obtained via NH 4 HF 2 -etching and surfactant-templating process. By using the different cationic surfactant (C n TAB), we fabricate the surfactant-templated zeolite with controllable mesopores, and improve its adsorption capacity for toluene. In addition, the modified zeolite’s hydrophobicity is enhanced, and it maintains a high adsorption capacity in a complex humid environment.
研究领域:
材料科学
·
环境工程
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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）