COMBUSTION AND FLAME
·
2021
·
IF 4.185
Zhi-Hao Jin,Jin-Tao Chen,Wang Li,Shu-Bao Song,Jiu-Zhong Yang,Zhen-Yu Tian
Owing to significant advantages over traditional biofuels, 2-methylfuran (MF) has arisen extensive interest as next generation biofuels . Atmospheric pressure pyrolysis of a 1:1 blend of MF with a three-component (3C) surrogate jet fuel was conducted in a flow tube using synchrotronphotoionization and molecular beam mass spectrometry techniques within a temperature range of 898–1223 K. Therein, the 3C surrogate fuel consists of 66.2% n-dodecane (NC 12 H 26 ), 18.0% 1,3,5-trimethylcyclohexane (T135MCH) and 15.8% n-propylbenzene (NPB, A1C 3 H 7 ). The detailed kinetic model including 579 species and 3474 reactions was developed via validating against both measured and literature data with reasonable agreement. MF exhibits no obvious influence on the 3C components pyrolysis . However, 3C mixtures play an important roles in MF decomposition: lower initial temperature and different decomposition pathways. In the meantime, n-propylbenzene (NPB) pyrolysis curve in 3C and 3C+MF significantly transfers to low temperature zone after 1000 K in contrast to pure NPB, while smaller change was found in the decomposition curve of n-dodecane. Compared with 3C pyrolysis, 3C+MF blends have less formation of aromatic species and light hydrocarbons except for vinylacetylene (C 4 H 4 ) and acetylene (C 2 H 2 ). Allyl radical (C 3 H 3 ) has significant roles in benzene ring formation. The combination of allyl radical with propargyl radical producing benzene and H radical (aC 3 H 5 + C 3 H 3 = A1 + 2H) has the highest contribution to the benzene formation in both 3C and 3C+MF. Moreover, most of naphthalene (A2) formation is also related to C 3 H 3 radical via reaction: A1CH 2 + C 3 H 3 = A2 + H, rather than via HACA (hydrogen abstraction carbon addition) reaction. Interaction of fuel blends was mainly presented through the common and important sensitive reactions which are much to do with CH 3 and H radicals. The overview of product distribution was investigated by providing comparisons of carbon conversion rates during the pyrolysis of 3C and 3C+MF. These results will be helpful to better understand the pyrolysis properties of MF/jet fuel surrogate blends and could contribute to developing new generation biofuels for aviation.
研究领域:
燃料化学
·
燃烧动力学
·
生物燃料
·
能源化学
·
反应机理
·
质谱分析
✓ 已验证
DOI
高影响因子
RUSSIAN JOURNAL OF GENERAL CHEMISTRY
·
2021
·Vol. 91
·期 4
·726-731
·
IF 0.868
Xu Y.,Hu Y.,Bao Q.,Zhang J.,Liu B.,Zhang Z.,Zhang Q.,Zhang H.
Copper phyllosilicate has been synthesized from a solution of sodium silicate and copper nitrate by co-precipitation under acidic conditions followed by reduction under H 2 flow for using it as the Cu/SiO 2 catalyst. The catalyst has been characterized by XRD, XPS, FTIR and Raman spectra, EDS, BET, and TEM. It is confirmed that only copper phyllosilicate and SiO 2 exist in the catalyst precursor, and there has been no CuO. Physical and chemical properties of Cu/SiO 2 catalyst have been evaluated. The Cu/SiO 2 catalyst has not only a large specific surface area and abundant mesopores but also the advantages of high dispersion of copper nanoparticles and the combination of Cu 0 and Cu + . The catalyst demonstrates high activity and selectivity in the reaction of 2-butanol dehydrogenation to methyl ethyl ketone.
研究领域:
催化化学
·
材料科学
·
物理化学
·
纳米材料
·
有机合成
✓ 已验证
DOI
高影响因子
IONICS
·
2016
·Vol. 22
·期 11
·2225-2233
·
IF 2.119
Lu Juanjuan,Liu Yuelin,Liu Xinhe,Lu Xiaoquan,Liu Xiuhui
In this article, we constructed an electrochemical sensor for highly sensitive determination of β-nicotinamide adenine dinucleotide (NADH) using the poly(diallyldimethylammonium chloride)-functionalized reduced graphene oxide nanocomposite modified electrode (PDDA-rGO/GCE). The nanocomposite was characterized by transmission electron microscopy, Fourier transform-infrared spectrometry, ultraviolet-visible absorption spectrometry, cyclic voltammetry, and electrochemical impedance spectroscopy. The experimental results demonstrated that the fabricated sensor exhibited excellent electrocatalytic activity on the oxidation of NADH with a decreased about 200 mV in overpotential and 5.0-fold increment in the oxidation peak current compared to a bare GCE. Applying cyclic voltammetry, a wide linear range from 1.0 × 10 −7 to 2.9 × 10 −3 M with low limit of detection (LOD) of 3.4 × 10 −8 M and high sensitivity of 463.3 μA mM −1 cm −2 were obtained, which was superior to other NADH electrochemical sensors reported previously. Furthermore, the fabricated NADH sensor possessed excellent selectivity, reproducibility, and stability. The oxidation mechanism of NADH at the PDDA-rGO/GCE was also discussed in detail.
A simple NADH sensing platform based on PDDA-rGO composite is constructed, which exhibits an ultra-low detection limit ( 3.4×10-8 M) towards the oxidation of NADH, and the electrochemical reaction mechanism of NADH is discussed in detail.
研究领域:
生物电化学
·
生物传感器
·
纳米生物技术
·
分子诊断
·
转化医学
·
电分析化学
✓ 已验证
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2013
·Vol. 131
·期 9
·
IF 1.395
Chang Su,Dezhen Zong,Lihuan Xu,Cheng Zhang
In this article, semi-interpenetrating polymer network (Semi-IPNs) based on nitrile rubber (NBR) and poly(methyl methacrylate- co -butyl acrylate) (P(MMA-BA)) were synthesized. The structure and damping properties of the prepared Semi-IPNs blends were characterized and by fourier transform infrared spectrum (FTIR), dynamic mechanical analysis (DMA), scanning electron microscopy (SEM), thermogravimetric analysis (TGA/DTG), and tensile mechanical properties. The results showed that interpenetrating network based on P(MMA-BA) and NBR was successfully obtained, which showed the improved thermal stability compared to NBR/P(MMA-BA)-based two-roll mill blends. Furthermore, Semi-IPNs showed significantly better the dynamic mechanical properties than that of the two-roll mill system. With the increasing feed ratio of BA and MMA during the preparation of Semi-IPNs, the loss peak position for P(MMA-BA) in NBR/PMMA IPNs shifted to a lower temperature from 20°C to −17°C, and when NBR in Semi-IPNs was accounted for 40 wt %, the dynamic mechanical thermal analysis showed that much more advanced damping material with wider temperature range (−30°C < T < 80°C) as tan δ > 0.45 can be achieved. Therefore, it was expected as a promising way to obtain the excellent damping materials with good oil-resisted properties according the Semi-IPNs system. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40217.
研究领域:
高分子材料科学
·
功能材料
·
复合材料
·
材料物理
·
阻尼材料
·
聚合物改性
✓ 已验证
DOI
高影响因子
Advances in Materials Science and Engineering
·
2018
·Vol. 2018
·期 1
·7252809
·
IF 1.372
Van-Tuan Mai,Quang-Bac Hoang,Xuan-Dung Mai
Cost-effective methods for preparing ZnO nanostructures are of importance for the deployment of ZnO in many applications including n-type conduits, catalysts, nanophosphor, and optoelectronics. Herein, we present a room-temperature sol-gel method with the aid of ultrasonication to prepare white-emitting ZnO nanoparticles (NPs). X-ray diffraction and electron microscopic analyses revealed that the size and shape of ZnO NPs can be controlled simply by changing the concentration of the Zn precursor. The ZnO NPs had a broad photoluminescence emission, ranging from 450 nm to 800 nm, while their composite in PMMA matrix showed an enhancement in the red region induced by ZnO-PMMA interfacial band-bending effects. The results demonstrated herein promise a simple tool for control over size, shape, and emission of ZnO materials for diverse applications.
研究领域:
材料科学
·
纳米技术
·
光电子学
·
高分子化学
·
发光材料
✓ 已验证
DOI
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2013
·
IF 3.535
Kelei Zhuo,Yujing Wei,Jingjing Ma,Yujuan Chen,Guangyue Bai
Several alkylmethylimidazolium tetraphenylborates (C n mim-TPB, n = 2–10) were synthesized and explored as ion exchangers in plasticized PVC membranes with very attractive sensing behaviors. And then a series of ion-selective electrodes (ISEs) were prepared and their potentiometric properties were investigated. The proposed electrodes exhibited Nernstian responses to alkylmethylimidazolium-based ionic liquid cations [C n mim] + . These electrodes were successfully applied in the determination of thermodynamic parameters of ionic liquids in aqueous solutions and in the detection of [C n mim] + in tap water and distilled water with satisfactory results. For the as-prepared ISEs, one special and important relationship was observed between the selectivity coefficients and the length of alkyl side chains of interfering cations [C n mim] + . The proper understanding of this relationship should facilitate the development of new method for the determination of ionic liquids using ISEs.
研究领域:
分析化学
·
电化学
·
环境监测
·
离子传感
·
药物分析
·
水处理
·
生物传感器
·
物理化学
✓ 已验证
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2017
·Vol. 134
·期 46
·45484
·
IF 1.86
Teng Xue,Erjun Tang,Jian Zhou,Ruitao Han,Shaojie Liu
A coordinating ionic liquid (IL), 1-[(diethyl amine)amine]ethyl-3-methyl imidazolium chloride ([N 3 MIM]Cl), was prepared as an alternative to a simple organic ligand to coordinate to copper(I) bromide (CuBr). We, thereby, obtained a novel catalyst for atom transfer radical polymerization (ATRP) reactions. This catalyst was applied to the ATRP of methyl methacrylate in the IL 1-allyl-3-methyl imidazolium chloride ([AMIM]Cl). The chemical structures of the ILs obtained were confirmed by Fourier transform infrared spectroscopy, mass spectrometry, and 1 H-NMR analyses. The coordination ability of [N 3 MIM]Cl was assessed by cyclic voltammetry, and the redox potential of [N 3 MIM]Cl–CuBr was −0.507 V. The [N 3 MIM]Cl–CuBr complex was expected to be a markedly more active catalyst than the amine DETA–CuBr complex. The coordination mode toward CuBr was also examined. The [N 3 MIM]Cl–CuBr catalyst system showed good controllability in the aforementioned ATRP reaction in [AMIM]Cl. The Cu catalyst was easily separated from the obtained polymer with the coordinating IL as a ligand. Consequently, the coordinating IL overcame the shortcomings of traditional organic ligands, such as poor compatibility with IL media and poor separation of the catalyst from the polymer; this makes it highly promising for applications in the ATRP field. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45484.
研究领域:
高分子化学
·
催化化学
·
功能材料
·
绿色溶剂
·
配位化学
·
电化学
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Shiqi Sun,Yanjun Chen,Qiang Bai,Zhen Tian,Que Huang,Changcheng Liu,Shengnan He,Yaxiong Yang,Yanzhong Wang,Li Guo
Researchers are accustomed to utilizing traditional solid-state and sol–gel routes to synthesize Na 3 V 2 (PO 4 ) 3 (NVP). No regulation mechanism is proposed to illustrate the growth process of NVP in solvothermal environment. In current work, uniform spherical particles with positive charge are synthesized by molecular self-assembly of nanosphere micelles using structural guiding agent polyethylene glycol (PEG) and surfactant Cetyltrimethylammonium bromide (CTAB). Nanoflower-shaped NVP sample is successfully prepared in the 100 % methyl alcohol medium, derived from the plate V 2 O 5 (negative charge) combining with the nuclear nanospheres (positive charge) with the induction of electrostatic attraction. Based on the multi-dimensional tests and molecular dynamic calculation, the protective mechanism of polar solution for NVP system is proposed for the first time, that is, methanol solvent system can better protect the morphological features of NVP than water environment to maintain the original special nanoflower morphology. Due to the distinctive and stabilized nanoflower construction, the optimized NVP60 sample can provide more extra active sites for the efficient de-intercalation of Na + and possess a large contacting area with electrolyte, resulting in the facilitated kinetic characteristics and superior electrochemical performance. The optimized NVP60 cathode possesses superior sodium storage property in both half cell and full cell. This work proposes a synergetic strategy combining theory and experiment to design and synthesize the modified NVP-based cathode materials from the molecular bonding aspect, further promoting the development of high performance cathode for SIBs.
研究领域:
材料科学
·
电化学
·
纳米材料
·
能源存储
·
无机化学
·
计算材料学
·
电池技术
✓ 已验证
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2011
·
IF 3.723
Hui Wang,Yuming Huang
Prussian-blue (PB)-modified γ-Fe 2 O 3 magnetic nanoparticles (PBMNPs) were successfully synthesized based on electric interactions between negatively charged [Fe(CN) 6 ] 4− and positively charged γ-Fe 2 O 3 nanoparticles. The in situ PB coating was generated by the coordinating reaction between the adsorbed [Fe(CN) 6 ] 4− and the ferric ions on the surface of γ-Fe 2 O 3 NPs. The as-prepared PBMNPs were characterized by FT-IR, XRD, TEM, and used to remove organic pollutants from aqueous solution, namely, using methylene blue (MB) as model compound. The experimental results showed that the target compound could be removed efficiently from solution over a wide pH range from 3 to 10 in the presence of PBMNPs as peroxidase-like catalyst and H 2 O 2 as oxidant. Under optimal conditions, MB could be removed completely after 120 min of reaction at 298 K; the chemical oxygen demand (COD) removal efficiency and the total organic carbon (TOC) abatement efficiency were 53.6% and 35%, respectively. Furthermore, the PBMNPs catalysts showed high magnetization, temperature tolerance, long-term storage and operational stability, and they could be readily separated from solution by applying an external magnetic field. Finally, a possible reaction mechanism for MB degradation was also discussed.
研究领域:
环境科学
·
纳米材料学
·
催化化学
·
水处理技术
·
环境功能材料
✓ 已验证
DOI
高影响因子
MACROMOLECULAR CHEMISTRY AND PHYSICS
·
2019
·Vol. 220
·期 18
·1900299
·
IF 2.622
Huidong Yang,Hong Wang,Jingang Feng,Yumin Ye,Wenna Liu
Asymmetric divinyl monomers are attractive candidates for constructing functional polymer thin films owing to their ability to undergo further reactions after polymerization. Here, the first solventless synthesis of poly(allyl methacrylate) (PAMA) film with retention of abundant allyl groups using initiated chemical vapor deposition (iCVD) is reported. It is demonstrated that lower substrate and filament temperatures lead to better allyl retention, while higher temperatures lead to intramolecular cyclization. The retained allyl groups can be further crosslinked under UV light, and the crosslinking degree can be easily tuned by adjusting the exposure time. Patterning of iCVD PAMA films with 20 µm resolution using a TEM grid as photomask is also demonstrated. The reported synthesis method suggests possible solventless incorporation of AMA in thin films as a latent crosslinker or anchoring sites for further functionalization. The solventless patterning can also extend patterning technique to solvent-sensitive and non-planar substrates.
研究领域:
高分子材料科学
·
表面化学
·
功能薄膜
·
光响应材料
·
生物医学工程
✓ 已验证
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2021
·Vol. 139
·期 1
·51418
·
IF 3.125
Lan Hao,Xulin Cui,Xiaoli Wu,Jingtao Wang,Yifan Li,Wenpeng Li,Xingzhong Cao,Haoqin Zhang
Efficient separation of aromatic-aliphatic hydrocarbon mixtures has long been an important topic in chemical industries. Organic nanofiltration (OSN) has been revealing great promise in separating solvent mixtures that has not been effectively resolved by the state-of-the-art technologies. Herein, novel OSN membranes are designed for the separation of toluene and n -heptane. Polyamide active layer with diaminonaphthalene as the aqueous phase monomer is prepared by interfacial polymerization for the first time. The addition of polydimethylsiloxane gutter layer, as well as the combination of spin coating technique and macroporous substrate, renders the membranes with loose and defect-free architectures. The as-designed membranes achieve a rather high selectivity of toluene over n -heptane (>4) together with ultra-high toluene permeance (>180 L m −2 h −1 bar −1 ). These membranes also present excellent stability in the long-term operation.
研究领域:
材料科学
·
膜分离技术
·
化学工程
·
纳米技术
·
高分子化学
·
工业催化
·
绿色化学
✓ 已验证
DOI
高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2016
·
IF 5.557
Jiayou Liao,Zhi Wang,Ming Wang,Chengyun Gao,Song Zhao,Jixiao Wang,Shichang Wang
An ion-exchange material – Poly(diallyldimethylammonium carbonate) (PDDACA) containing mobile carbonate has been prepared and it has been blended in a fixed carrier membrane material – polyvinylamine (PVAm) containing abundant amine-group to adjust the carrier microenvironment of the fixed carrier membrane. It makes the mobile carrier cruise around the fixed carrier. On one hand, the CO 2 can be transported continuously in the swing area of fixed carrier through the mobile carriers, the passivity of fixed carrier can be overcome and the utilization efficiency of fixed carrier can be enhanced. On the other hand, a loose and low crystalline system will be obtained by blending two polymers, the number of effective mobile carrier will be increased with mobile carriers unlocking from the crystalline area, and the loose and low crystalline system will provide a good environment for the movement of mobile carriers. These are conducive to enhance the performance of blend membrane in comparision with single polymer membrane. The CO 2 permeance and CO 2 /N 2 selectivity of PVAm-PDDACA membrane, which concurrently contains fixed amine carriers and movable carbonate carriers, can reach 909 GPU and 102 at 0.11 MPa, respectively. The performance of PVAm-PDDACA membrane is enhanced obviously in comparision with PVAm membrane and PDDACA membrane.
研究领域:
膜科学与技术
·
气体分离
·
高分子材料
·
化学工程
·
环境化工
·
能源材料
·
功能材料
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）