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101.
A mathematical model was developed to represent pyrolysis. The components of primary and secondary pyrolysis reactions were simply lump into different groups and were represented through a set of pseudo‐first‐order reactions. This study presents an algorithm to estimate the kinetic parameters using Monte‐Carlo (MC) simulation. The combination of an analytical reaction model and the MC simulation technique rapidly generates a large number of numerical values. Results show that MC‐simulated data and experimental data are in fair agreement. Though the technique developed in this study proved to have potential, more experimental data are needed to check the robustness of the model. © 2011 Canadian Society for Chemical Engineering 相似文献
102.
Ahmed Jalal Uddin Akihira Watanabe Yasuo Gotoh Takeshi Saito Motoo Yumura 《大分子材料与工程》2012,297(11):1114-1123
PVA is reinforced with SWCNTs using green tea extract as a dispersant to achieve good dispersion of the SWCNTs in an organic solvent and finally high‐performance composite fibers. A combination of green tea extract/DMSO/SWCNT/PVA is found to disperse larger aggregates of SWCNTs to individual or thin bundles of a few nanotubes. Incorporation of 0.5 wt% SWCNTs into PVA fibers yields a tensile strength of 2.42 GPa, a Young's modulus of 46 GPa, toughness of 105 J · g?1 at a failure strain of 11%, and a loop strength of 245 MPa, much higher than the values of commercial PVA fibers. The incorporation of highly dispersed SWCNTs suppresses the fibrillation tendency of the PVA fibers. The applied load is effectively transferred from the matrix to the SWCNTs.
103.
An efficient fully bio‐based reactive diluent for epoxy thermosets: 2‐[(Oxiran‐2‐ylmethoxy) methyl] furan versus a petroleum‐based counterpart 下载免费PDF全文
Furfuryl alcohol and bio‐based epichlorohydrin were used to prepare a fully bio‐based reactive diluent, 2‐[(oxiran‐2‐ylmethoxy) methyl] furan (FOM). After spectral characterization, FOM was blended with epoxy resin, diglycidylether bisphenol A (DGEBA), at different ratios for reducing the viscosity. For a comparison, Cardura (one of the most common commercial reactive diluents), was separately incorporated to DGEBA. Amine‐curing process of the blends was recorded by FTIR and DSC. Similar trends of curing progression for DGEBA containing the reactive diluents were observed. Thermogravimetric analysis and dynamic mechanical thermal analysis, mechanical (hardness, adhesion, and stress–strain) and morphological properties were also investigated to study characteristics of the epoxy matrices formulated with FOM or Cardura. It was concluded that FOM could be considered as an efficient reactive diluent in formulations of polymer composites, structural adhesives and surface coatings based on epoxy resins. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44957. 相似文献
104.
Ahmed Jalal Samed Takayuki Tanaka Shin Hamada Keita Ikeue Masato Machida 《Catalysis communications》2009,10(15):1995-1999
Catalytic light-off of a stream of NO, H2, CO in an excess O2 has been studied over various metal oxides loading 1 wt% Pt. Because a low-surface area Y2O3 (<5 m2 g−1) was found to exhibit the highest de-NOx activity, a mesoporous Y2O3 was then synthesized from an yttrium-based surfactant mesophase templated by dodecyl sulfate , which was anion-exchanged by acetate (AcO = CH3COO−). The product showed a 3-D mesoporosity with a large surface area (396 m2 g−1) and the Pt-supported catalyst achieved much improved light-off characteristics suitable for the low-temperature de-NOx in the presence of CO and excess O2. 相似文献
105.
The undecimated wavelet decomposition and its reconstruction. 总被引:2,自引:0,他引:2
Jean-Luc Starck Jalal Fadili Fionn Murtagh 《IEEE transactions on image processing》2007,16(2):297-309
This paper describes the undecimated wavelet transform and its reconstruction. In the first part, we show the relation between two well known undecimated wavelet transforms, the standard undecimated wavelet transform and the isotropic undecimated wavelet transform. Then we present new filter banks specially designed for undecimated wavelet decompositions which have some useful properties such as being robust to ringing artifacts which appear generally in wavelet-based denoising methods. A range of examples illustrates the results. 相似文献
106.
Abdul Jalal Jinrui Sun Yeqing Chen Chunguo Fan Jinyi Liu Changquan Wang 《International journal of molecular sciences》2022,23(13)
Pseudo-response regulators (PRRs) are the important genes for flowering in roses. In this work, clock PRRs were genome-wide identified using Arabidopsis protein sequences as queries, and their evolutionary analyses were deliberated intensively in Rosaceae in correspondence with angiosperms species. To draw a comparative network and flow of clock PRRs in roses, a co-expression network of flowering pathway genes was drawn using a string database, and their functional analysis was studied by silencing using VIGS and protein-to-protein interaction. We revealed that the clock PRRs were significantly expanded in Rosaceae and were divided into three major clades, i.e., PRR5/9 (clade 1), PRR3/7 (clade 2), and TOC1/PRR1 (clade 3), based on their phylogeny. Within the clades, five clock PRRs were identified in Rosa chinensis. Clock PRRs had conserved RR domain and shared similar features, suggesting the duplication occurred during evolution. Divergence analysis indicated the role of duplication events in the expansion of clock PRRs. The diverse cis elements and interaction of clock PRRs with miRNAs suggested their role in plant development. Co-expression network analysis showed that the clock PRRs from Rosa chinensis had a strong association with flowering controlling genes. Further silencing of RcPRR1b and RcPRR5 in Rosa chinensis using VIGS led to earlier flowering, confirming them as negative flowering regulators. The protein-to-protein interactions between RcPRR1a/RcPRR5 and RcCO suggested that RcPRR1a/RcPRR5 may suppress flowering by interfering with the binding of RcCO to the promoter of RcFT. Collectively, these results provided an understanding of the evolutionary profiles as well as the functional role of clock PRRs in controlling flowering in roses. 相似文献
107.
108.
109.
Zohreh Merati Jalal Basiri Parsa Rasoul Babaei-Sati 《International Journal of Hydrogen Energy》2018,43(45):20993-21005
As known, a good support enhances the activity and durability of any catalyst. In the current study, polypyrrole (PPY)/nanocomposite (MWCNTs and Al2O3) films were fabricated by electrochemical polymerization of pyrrole solution with a certain amount of nanoparticles on titanium substrates and were used as new support materials for Pt catalyst. The modified electrodes were characterized by Fourier transform infrared (FT-IR) spectroscopy, field-emission scanning electron microscopy (FE-SEM) and energy dispersive X-ray analysis (EDX) techniques. High catalytic activity and long-time stability toward methanol oxidation of Pt/PPY–MWNTs-αAl2O3 catalyst have also been verified by cyclic voltammetry results and chronoamperometric response measurements. This catalyst exhibits a vehemently high current density (345.03 mA cm?2) and low peak potential (0.74 v) for methanol oxidation. Other electrochemical measurements (electrochemical impedance spectroscopy (EIS), CO stripping voltammetry and Tafel test) clearly confirmed that Pt/PPY–MWNTs-αAl2O3/Ti electrode has a better performance toward methanol oxidation compared to the other electrodes and that can be used as a promising electrode material for application in direct methanol fuel cells (DMFCs). 相似文献
110.
Monteil-Rivera F Paquet L Halasz A Montgomery MT Hawari J 《Environmental science & technology》2005,39(24):9725-9731
RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine) and HMX (octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine) are cyclic nitramines ((CH2NNO2)n; n = 3 or 4, respectively) widely used as energetic chemicals. Their extensive use led to wide environmental contamination. In contrast to RDX, HMX tends to accumulate in soils due to its unique recalcitrance. In the present study, we investigated the potential of zerovalent iron (ZVI) to transform HMX under anoxic conditions. HMX underwent a rapid transformation when added in well-mixed anoxic ZVI-H2O batch systems to ultimately produce formaldehyde (HCHO), ammonium (NH4+), hydrazine (NH2NH2), and nitrous oxide (N2O). Time course experiments showed that the mechanism of HMX transformation occurred through at least two initial reactions. One reaction involved the sequential reduction of N-NO2 groups to the five nitroso products (1NO-HMX, cis-2NO-HMX, trans-2NO-HMX, 3NO-HMX, and 4NO-HMX). Another implied ring cleavage from either HMX or 1NO-HMX as demonstrated by the observation of methylenedinitramine (NH(NO2)CH2NH(NO2)) and another intermediate that was tentatively identified as (NH(NO2)CH2N(NO)CH2NH-(NO2)) or its isomer (NH(NO)CH2N(NO2)CH2NH(NO2)). This is the first study that demonstrates transformation of HMX by ZVI to significant amounts of NH2NH2 and HCHO. Both toxic products seemed to persist under reductive conditions, thereby suggesting that the ultimate fate of these chemicals, particularly hydrazine, should be understood prior to using zerovalent iron to remediate cyclic nitramines. 相似文献