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1.
Linear low‐density polyethylene (LLDPE), based on butene‐1 or hexene‐1, was irradiated with γ‐rays under vacuum or in the presence of air. The study focused on the influence of the dose rate and the γ‐dose on the thermal properties of LLDPE. Differential scanning calorimetry, thermogravimetric analysis (TGA), and TGA/FTIR techniques were used to address the thermal behavior as a result of γ‐irradiation. During this irradiation, competition between crosslinking and scission reactions, subsequent to oxidation reactions, occurred in the polymeric material, which strongly depends on the experimental conditions. A decrease of the crystallinity for γ‐irradiated samples was observed in particular for samples irradiated under vacuum. This observation may be explained by increased hindrance of segment mobility due to crosslinking reactions that prevent crystal growth. TGA investigations revealed an enhancement of the thermal stability for samples irradiated under vacuum but not for those irradiated in air. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2790–2795, 2006 相似文献
2.
Magatte Diagne Mamadou Gueye Anicet Dasilva Loic Vidal Adams Tidjani 《Journal of Materials Science》2006,41(21):7005-7010
Nanocomposites of polypropylene-graft-maleic anhydride/clay were prepared by melt blending in an extruder mixer. The nanoscale dispersion of the clay in the polymer was analysed by wide-angle X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results of XRD and TEM showed that the nanocomposites obtained were a kind of intercalated-delaminated structures side by side with different dominant states, depending on the clay used and on the processing conditions. The consequences of photo-oxidation on the thermal stability and fire retardant properties of the nanocomposites were investigated using thermogravimetric analysis and cone calorimetry tests. It appeared that this degradation dramatically affected the important properties of the nanocomposites. A loss of thermal stability and fire retardant performance was observed. This was ascribed to scission reactions that occurred during the oxidative degradation prior to thermal and fire tests. 相似文献
3.
Abba Bala Namata Idouhli Rachid Ilagouma Amadou Tidjani Abouelfida Abdesselam Khadiri MohyEddine Romane Abderrahmane 《Protection of Metals and Physical Chemistry of Surfaces》2021,57(3):619-633
Protection of Metals and Physical Chemistry of Surfaces - In the present study, we evaluated the effect of corrosion inhibition of ethanol extracts from Endostemon tereticaulis and Hyptis spicigera... 相似文献
4.
Polypropylene PP (high and low crystallinity) was λ-oxidized, in the presence of air, using different dose rates (from 2 to 100 rad/s). Oxidation outcomes were identified and quantified by FTIR spectroscopy coupled with derivatization reactions (NO and SF4). The difficulty to separate secondary and tertiary hydroperoxides from FTIR measurements after NO treatment was addressed. Polymer physical degradation was also monitored during the λ-irradiation process. GPC was used to follow molecular weight changes and tensile tests for elongation at break modifications. Comparison of the extent of oxidation product for-mation over λ-irradiation allowed us to investigate the importance of λ-dose rate on chemical and physical changes of PP. From this, different mechanisms of ketone and ester formation were examined; relationship between the molecular weight changes and the elongation at break modifications was also investigated. © 1996 John Wiley & Sons, Inc. 相似文献
5.
A high pressure shock tube study of n-propylbenzene oxidation and its comparison with n-butylbenzene
Daniel Darcy Colin J. Tobin Kenji Yasunaga John M. Simmie Judith Würmel Wayne K. Metcalfe Tidjani Niass Syed S. Ahmed Charles K. Westbrook Henry J. Curran 《Combustion and Flame》2012,159(7):2219-2232
Ignition delay times have been measured for mixtures of n-propylbenzene in air (≈21% O2, ≈79% N2) at equivalence ratios of 0.29, 0.48, 0.96 and 1.92 and at reflected shock pressures of 1, 10 and 30 atm in a heated high-pressure shock tube over a wide temperature range (1000–1600 K). The effects of reflected shock pressure and of equivalence ratio on ignition delay time were determined and common trends highlighted. Simulations were carried out using the n-propylbenzene sub-mechanism contained in an n-butylbenzene reaction mechanism available in the literature. This kinetic model was improved by including pressure dependent reactions which were not in place previously and the addition of the NUI Galway C0–C4 sub-mechanism. These simulations showed very good agreement with the experimental data. Additionally a comparison is made with experimental data previously obtained and published for n-butylbenzene over the same range of conditions and common trends are highlighted. 相似文献
6.
Diène Ndiaye Laurent M. Matuana Sandrine Morlat‐Therias Loïc Vidal Adams Tidjani Jean‐Luc Gardette 《应用聚合物科学杂志》2011,119(6):3321-3328
In this research, polypropylene/wood‐flour composites (WPCs) were blended with different contents of wood and/or maleated polypropylene (MAPP) and clay. We found that the addition of MAPP or clay in the formulation greatly improved the dispersion of the wood fibers in the composite; this suggested that MAPP or clay may have played the role of an adhesion promoter in the WPCs. The results obtained with clay indicate that it also acted as a flame retardant. The thermal tests carried out with the produced samples showed an increased crystallization temperature (Tc), crystallinity, and melting temperature (Tm) with wood loading. The increase of the two former parameters was explained by the incorporation of wood flour, which played the role of nucleating agent and induced the crystallization of the matrix polymer. On the other hand, the Tm increase was ascribed to the insulating properties of wood, which hindered the movement of heat conduction. The effects of UV irradiation on Tm and Tc were also examined. Tc increased with UV exposure time; this implied that UV degradation generated short chains with low molecular weight that could move easily in the bulk of the sample and, thus, catalyze early crystallization. The flexural strength and modulus increased with increasing wood‐flour content. In contrast, the impact strength and tensile strength and strain decreased with increasing wood‐flour content. All of these changes were related to the level of dispersion of the wood flour in the polymeric matrix. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 相似文献
7.
研究了烘烤对于花生蛋白溶解性、浸泡(时间、效率)以及不同水/固形物(花生)比对总可提取固形物的影响。当烘烤温度为90~120℃,烘烤10min时,蛋白溶出率最高。最佳的浸泡时间和固形物(花生)/水比分别为6h,1:2。对于总可提取固形物而言,以其组成和粘度(2.1cps)为基准,花生/水比为1:8时最好。 相似文献
8.
This paper presents a symmetric isoparametric finite element formulation for the inverse problem of aquifer transmissivity calculation with known piezometric head. An important aspect of the present formulation is that the groundwater flow equation describing the aquifer behavior is transformed into a second-order differential equation by introducing an artificial variable φ. The two-dimensional, line and transition elements derived based on the weak formulation of this transformed equation possess symmetric matrices. In the formulation of the line elements φ and its derivative in η direction are retained as primary variables. This permits modelling of sudden changes in aquifer width. The transition elements provide a natural connecting link between the two-dimensional elements and the line elements. The line elements provide an efficient means of modelling aquifers with unidirectional flow. Numerical examples are given. A comparison of the results obtained here with the Galerkin finite element solution (nonsymmetric formulation) clearly demonstrates the superiority of the formulation presented here. 相似文献
9.
The present work concerns the interplay of the degradation mechanism and the nature of the interaction between microorganisms and substrate. The biodegradation of polycaprolactone films by a pure strain of microorganisms isolated from an industrial composting unit for household refuse was studied in minimal medium with the polymer as sole carbon source. In conditions where the polymer surface is colonized and a biofilm is formed (under a low stirring rate), polymer weight loss is limited, whereas total degradation is observed when stirring conditions prevent biofilm formation. In the first case, holes are observed in the degraded film and a polysaccharide responsible for microorganism adhesion was identified by FTIR. SEM observation of the polymer surface as a function of the degradation time suggests that the crystalline and amorphous phase are degraded at about the same rate in the first case, whereas the amorphous phase is preferentially degraded in the latter. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 1334–1340, 2002 相似文献
10.
The photo‐oxidation behavior under natural and accelerated conditions of polypropylene/layered silicate nanocomposite is studied in this article. The nanocomposites are prepared via simple melt mixing (extrusion and injection molding). The structure obtained is very dependent on the preparation mode and the modified clay used; mostly, exfoliation structure is produced. The nanocomposites start their photo‐degradation earlier than the control samples polypropylene and polypropylene‐graft‐maleic anhydride with a higher oxidation rate for specimen produced by injection molding. This is explained by the presence of organiphilic‐modified montmorillonite layers that trap the oxygen, increasing the oxygen pressure in the bulk and leading to a decrease of the induction period. Contrary to the control samples that display auto acceleration in their oxidation kinetics, the nanocomposites show a slight tendency to a plateau indicating a slowing down of the photo‐oxidation process. This is ascribed to oxygen starvation that occurs in the nanocomposite. The acceleration factor is found to be higher for the nanocomposite comparatively of the control samples. With the aid of SF4 and NO treatments, the mechanism of photo degradation was found to be similar in PPgMA and its nanocomposites. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 相似文献