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Thermal Degradation (thermal + degradation)
Terms modified by Thermal Degradation Selected AbstractsA Kinetic Study on the Thermal Degradation of Multi-Walled Carbon Nanotubes-Reinforced Poly(propylene) CompositesMACROMOLECULAR MATERIALS & ENGINEERING, Issue 4 2004Min-Kang Seo Abstract Summary: The influence of the multi-walled carbon nanotubes (MWNTs) content on the thermal degradation behavior of MWNTs-reinforced poly(propylene) (PP) composites was investigated by using non-isothermal thermogravimetric analysis (TGA). Kinetic parameters of degradation were evaluated by using the Flynn-Wall-Ozawa iso-conversional method and the pseudo first-order method. As a result, compared with pristine PP, MWNTs-PP nanocomposites have lower peak temperatures of degradation, narrower degradation temperature ranges and a higher amount of residual weight at the end of the degradation, which is likely to be a result of specific interactions between complimentary functional groups. The values of the reaction order of MWNTs-PP nanocomposites determined by the Kissinger method are close to 1 in the non-isothermal degradation process. There is a good correlation between the Ea in region II and the peak temperature of degradation for the composites. Activation energies for degradation of different contents of MWNTs-filled PP nanocomposites as a function of conversion. [source] Rational, Facile Synthesis and Characterization of the Neutral Mixed-Metal Organometallic Oxides Cp*2MoxW6,xO17 (Cp* = C5Me5, x = 0, 2, 4, 6)EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 34 2009Gülnur Taban-Çal Abstract The reaction of the bis(pentamethylcyclopentadienyl)pentaoxidodimetal complexes Cp*2M2O5 with four equivalents of Na2M,O4 (M, M, = Mo, W) in acidic aqueous medium constitutes a soft and selective entry into neutral Lindqvist-type organometallic mixed-metal oxides Cp*2MoxW6,xO17 [x = 6 (1), 4 (2), 2 (3), 0 (4)]. The identity of the complexes is demonstrated by elemental analyses, thermogravimetric analyses and infrared spectroscopy. Thermal degradation of 1,4 up to above 500 °C leads to Mox/6W1,x/6O3. The molecular identity and geometry of compound 2 is further confirmed by a fit of the powder X-ray diffraction pattern with a model obtained from previously reported single-crystal X-ray structures of 1 and 4, with which 2 is isomorphous. DFT calculations on models obtained by replacing Cp* with Cp (I,IV) validate the structural assignments and assist in the assignment of the M,M,,O vibrations. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source] Synthesis, cure kinetics, and thermal properties of the Bis(3-allyl-2-cyanatophenyl)sulphoxide/BMI blendsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008G. Anuradha Abstract A novel allyl functionalized dicyanate ester resin bearing sulfoxide linkage was synthesized. The monomer was characterized by Fourier Transform Infrared (FT-IR) Spectroscopy, 1H-, and 13C Nuclear Magnetic Resonance (NMR) spectroscopy and elemental analysis. The monomer was blended with bismaleimide (BMI) at various ratios in the absence of catalyst. The cure kinetics of one of the blends was studied using differential scanning calorimetry [nonisothermal] and the kinetic parameters like activation energy (E), pre-exponential factor (A), and the order of the reaction (n) were calculated by Coats-Redfern method and compared with those calculated using the experimental Borchardt-Daniels method. The thermal stability of the cured dicyanate, BMI, and the blends was studied using thermogravimetric analyzer. The initial weight loss temperature of dicyanate ester is above 380°C with char yield of about 54% at 800°C. Thermal degradation of BMI starts above 463°C with the char yield of about 68%. Inclusion of BMI in cyanate ester increases the thermal stability from 419 to 441°C. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Catalytic conversion of waste plastics: focus on waste PVCJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 9 2007Mark A Keane Abstract Effective waste management must address waste reduction, reuse, recovery/recycling and, as the least progressive option, waste treatment. The increase in plastic waste production is a serious environmental issue. Plastics consumption continues to grow and while plastic recycling has seen a significant increase since the early 1990s, consumption still far exceeds recycling. Waste plastic can, however, serve as a potential resource and, with the correct treatment, can be reused or serve as hydrocarbon raw material or as a fuel. PVC, highly versatile with many applications, is non-biodegradable and has a high Cl content (56% of the total weight). Waste PVC incineration is highly energy demanding and can result in the formation of toxic chloro-emissions with adverse ecological, environmental and public health impacts. The Cl component must be removed from any waste PVC derived gas or oil before it can be used. An overview of the existing waste plastic treatment technologies is provided with an analysis of the available literature on thermal and catalytic PVC degradation. Thermal degradation results in random scissioning of the polymer chains generating products with varying molecular weights and uncontrolled Cl content. There is a dearth of literature dealing with the catalytic dechlorination of PVC. A case study is presented to illustrate the role heterogeneous catalysis can play in PVC waste treatment. The efficacy of Pd/Al2O3 to promote PVC dechlorination is demonstrated, where a significant decrease (by up to a factor of 560) in the liquid fraction Cl content is recorded in addition to differences (relative to thermal degradation) in the gas phase product, i.e. higher C1C4 content with preferential alkane formation. Copyright © 2007 Society of Chemical Industry [source] THERMAL DEGRADATION KINETICS OF SUCROSE, GLUCOSE AND FRUCTOSE IN SUGARCANE MUST FOR BIOETHANOL PRODUCTIONJOURNAL OF FOOD PROCESS ENGINEERING, Issue 5 2006J. NOLASCO JR. ABSTRACT Thermal degradation of sugars contained in sugarcane must (21.5°Brix, pH 6.14) was evaluated at temperatures of 110, 120, 130 and 140C, using the thermal-death-time tube method, determining remaining sugars by high-pressure liquid chromatography. The study analyzed thermal degradation kinetics of both the total reducing sugars (TRS) and glucose and fructose individually. All curves of remaining sugars presented strong nonlinearity, with initial shoulder and final tail adjusted by an extended logistic model that was adapted for two species for TRS, and a simple logistic model for the monosaccharides. It was shown that rate constants are influenced by temperature according to two irreconcilable methods: the Arrhenius and the Bigelow methods. Obtained activation energies for fructose and glucose were quite coincident, 140.37 and 140.23 kJ/mol, respectively. Thermal resistance parameters were 21.59 and 21.61C, respectively. Comparison of the rate constants revealed that fructose degraded approximately 9,10 times faster than glucose. [source] Influence of the Composition on Crystal Phase and Thermal Behavior of trans -1,4-Butadiene/Isoprene CopolymersMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 23 2007Fabio Bertini Abstract Butadiene/isoprene copolymers were prepared using the catalyst system V(acac)3 -MAO. The structure of the comonomers is trans -1,4 and the butadiene and isoprene units are statistically distributed along the polymer chain. The attitude of the butadiene sequences to crystallize in the monoclinic form and to evolve in the hexagonal form is preserved in the copolymer for a certain range of composition. The temperature interval between the two endothermic events is progressively reduced by increasing the isoprene content. The monoclinic/hexagonal transition produces a considerable increase in the lamellar thickness of the polymers. Thermal degradation of the copolymers is influenced by the composition and takes place in two different stages: a series of cyclization and cross-linking reactions occur before the decomposition step. [source] Structure elucidation of thermal degradation products of amlodipineMAGNETIC RESONANCE IN CHEMISTRY, Issue 8 2007A. Siva Lakshmi Devi Abstract Thermal degradation of amlodipine base causes intramolecular reactions affording three cyclic products, referred to as AMLDEG-I, AMLDEG-II, and AMLDEG-III, respectively. AMLDEG-I is a cyclized product formed by intramolecular elimination of ammonia from amlodipine. AMLDEG-II is a positional isomer of AMLDEG-I. AMLDEG-III is also intramolecular cyclisation product. The three degradation products were isolated by column chromatography and characterized by FT-IR and 1H and 13C NMR spectroscopy data. The AMLDEG-III was crystallized and its structure was solved by single crystal X-ray diffraction (SXRD). Copyright © 2007 John Wiley & Sons, Ltd. [source] Effect of an epoxy octasilsesquioxane on the thermodegradation of an epoxy/amine systemPOLYMER INTERNATIONAL, Issue 1 2010Belén Montero Abstract Polyhedral oligomeric silsesquioxanes (POSS®) can be added to thermoplastic and thermostable polymers to obtain hybrid materials with only a minor tendency to suffer ignition. The aim of the work reported was to analyse the influence of an octafunctional POSS® in the pyrolysis of an epoxy/amine system as well as during the combustion process. Thermal degradation of the modified materials, with respect to the unmodified ones, was analysed using thermogravimetric analysis. As the content of POSS® increased the stability improved and the char/ceramic yields were higher. The Kissinger,Akahira,Sunose method was applied to the modified blends and it showed a decrease in the activation energy with POSS® content. Empirical kinetic models, as well as generalized master plots, were applied to explain the degradation mechanism for ternary blends. The limiting oxygen index parameter was measured to analyse the fire retardancy effect of POSS®: it increased from 24.3 to 25.4% with the addition of 2.5 wt% of POSS®. The mechanism of thermal degradation of the hybrid materials based on an epoxy resin is affected by the presence of the octaepoxy POSS®. Only small amounts of POSS® are necessary to enhance the combustion resistance of the system. Copyright © 2009 Society of Chemical Industry [source] Thermal degradation of a brominated bisphenol a derivativePOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 11-12 2003M. P. Luda Abstract The thermal degradation of 2,6,2,,6,,tetrabromo-4,4,-isopropylidene-di phenol (tetrabromobisphenol A) (TBBPA) has been investigated and a mechanism for its thermal degradation is suggested. TBBPA is a comonomer widely used in epoxy and in unsaturated polyester resins to impart fire retardance. These resins find a common use in electric and electronic equipment. The presence of bromine atoms is the key factor in fire retardant activity, while on the other hand it represents an ecological problem when pyrolytic recycling is programmed at the end of the useful life of such items. However, pyrolysis is the more advantageous recycling system for thermosetting resins and thus efforts should be made to control the pyrolysis in order to avoid or minimize the development of toxics. Homolytic scission of the aromatic bromine and condensation of aromatic bromine with phenolic hydroxyl are the main processes occurring in the range 270,340°C. A large amount of charred residue is left as a consequence of condensation reactions. HBr and brominated phenols and bisphenols are the main volatile products formed. Brominated dibenzodioxins structures are included in the charred residue and not evolved in the volatile phases. Copyright © 2003 John Wiley & Sons, Ltd. [source] Identification of heat-induced degradation products from purified betanin, phyllocactin and hylocerenin by high-performance liquid chromatography/electrospray ionization mass spectrometryRAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 18 2005Kirsten M. Herbach Betanin, phyllocactin (malonylbetanin) and hylocerenin (3-hydroxy-3-methylglutarylbetanin) were isolated from purple pitaya (Hylocereus polyrhizus [Weber] Britton & Rose) juice, and their degradation products generated by heating at 85°C were subsequently monitored by high-performance liquid chromatography/electrospray ionization tandem mass spectrometry. Thermal degradation of phyllocactin and hylocerenin in purified solution excluding the alleged protective effects by the juice matrix is reported for the first time. Betanin was predominantly degraded by hydrolytic cleavage, while decarboxylation and dehydrogenation were of minor relevance. In contrast, hylocerenin showed a strong tendency to decarboxylation and dehydrogenation, hydrolytic cleavage of the aldimine bond occurring secondarily. Phyllocactin degradation was most complex because of additional decarboxylation of the malonic acid moiety as well as generation and subsequent degradation of betanin due to phyllocactin demalonylation. Upon prolonged heating, all betacyanins under observation formed degradation products characterized by an additional double bond at C2C3. Hydrolytic cleavage of the aldimine bond of phyllocactin and hylocerenin yielded previously unknown acylated cyclo -dopa derivatives traceable by positive ionization, while application of ESI(,) facilitated the detection of a glycosylated aminopropanal derivative and dopamine, which have never been described before as betanin degradation products. Copyright © 2005 John Wiley & Sons, Ltd. [source] The influence of chain-ends on the thermal and rheological properties of some 40/60 PES/PEES copolymersPOLYMER ENGINEERING & SCIENCE, Issue 8 2009Lorenzo Abate Four random, differently ended (Cl, NH2, OH, and COO,), polyethersulfone/polyetherethersulfone (PES/PEES) copolymers were studied to investigate the influence of chain ends on thermal and rheological behaviors. The number average molar mass (Mn , 9500 g·mol,1) and the PES/PEES ratio (40/60) of all copolymers investigated were checked by 1H NMR spectra. Thermal degradations were carried out in the scanning mode and initial decomposition temperatures (Ti) and activation energy values of degradation (Ea) were obtained. Glass transition temperature (Tg) was determined by differential scanning calorimetry and complex viscosity (,*) by rheological measurements in isothermal heating conditions (T = 270°C). All parameters determined were largely affected by copolymer chain ends and decreased according to the same order, OH > NH2 > Cl > COO,. The results were discussed and interpreted. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers [source] Quantitative relation between shear history and rheological properties of LDPEADVANCES IN POLYMER TECHNOLOGY, Issue 4 2001Masayuki Yamaguchi The role of the applied processing equipment shear history on the rheological properties of low-density polyethylene was studied in detail. It was found that the shear history depresses the melt strength and the oscillatory shear modulus, especially the storage modulus in low frequency region. This phenomenon is not caused by lowering of the molecular weight, which remained the same as the original, for all shear history samples, indicating absence of mechanical/thermal degradation during processing. Furthermore, annealing the melt processed samples enhances both the melt strength and the oscillatory modulus to the values of the original, unsheared sample. Finally we applied shear history in a cone-and-plate rheometer and found that the growth curve of the storage modulus, which can be expressed by a simple equation, is determined by both the duration of the flow and the magnitude of the applied shear stress. © 2001 John Wiley & Sons, Inc. Adv Polym Techn 20: 261,269, 2001 [source] Flame retardation and thermal degradation of flame-retarded polypropylene composites containing melamine phosphate and pentaerythritol phosphateFIRE AND MATERIALS, Issue 5 2008Shun Zhou Abstract The flame retardation of polypropylene (PP) composites containing melamine phosphate (MP) and pentaerythritol phosphate (PEPA) was characterized by limiting oxygen index (LOI) and UL 94. The morphology of the char obtained from the combustion of the composites was studied by scanning electron microscopy (SEM). The thermal degradation of the composites was investigated using thermogravimetric (TG) analysis and real-time Fourier transform infrared (RTFTIR) spectroscopy. It has been found that the PP composites containing only MP do not show good flame retardancy even at 40% additive level. Compared with the PP/MP binary composites, all the LOI values of the PP/MP/PEPA ternary composites at the same additive loading increase, and UL 94 ratings of the ternary composites at suitable MP/PEPA ratios are raised to V-0 from no rating (PP/MP). The TG and RTFTIR studies indicate that the interaction occurs among MP, PEPA and PP. Copyright © 2008 John Wiley & Sons, Ltd. [source] Modelling thermal degradation of composite materialsFIRE AND MATERIALS, Issue 2 2007Javier Trelles Abstract A one,dimensional, transient thermal degradation heat transfer model for the response of composite materials when exposed to fire is presented. The model can handle layers of different materials. Material properties are functions of temperature. The reaction can be specified using Arrhenius-type parameters or by inputting a density,temperature relationship determined by any experimental technique such as thermogravimetric analysis. The model is validated against the experimental data presented in Boyer's 1984 dissertation. Overall, the model provides excellent agreement with the experimental data. It is shown that very little difference is found between results arrived at by Arrhenius kinetics and results obtained by specifying the easier to measure density,temperature relationship. From this it is concluded that this technique is a viable alternative to Arrhenius-type models. Copyright © 2006 John Wiley & Sons, Ltd. [source] Insight into the Role of Oxidation in the Thermally Induced Green Band in Fluorene-Based Systems,ADVANCED FUNCTIONAL MATERIALS, Issue 4 2007R. Grisorio Abstract The causes of the spectral instability of poly[9,9-dioctylfluoren-2,7-diyl-co-2,,7,-spiro(cyclohexane-1,9,-fluorene)] during thermal annealing in air, which leads to a green photoluminescence (PL) emission band, are investigated. The Igreen/Iblue ratio evolution (I,=,intensity) is found to be independent of the amount of monoalkylfluorene defects, despite the fact that their presence might be regarded as a trigger for the radical process leading to polymer degradation in the presence of a trace amount of metal catalyst. Furthermore, the absence of a correlation between the degree of oxidation of the material and the Igreen/Iblue ratio indicates that the spatial disposition of fluorenones formed during the thermal degradation of the material, rather than their amount, is to be strictly related to the Igreen/Iblue ratio. The evidenced formation of fluorenone agglomerates, which could be considered the cause for the consistent increase in the Igreen/Iblue ratio during a thermal oxidation of a polyfluorene, confirms that the radical mechanism can also involve dialkylfluorene systems. Finally, the higher resistance to thermal degradation shown by spirocyclohexane fluorene units with respect to dioctylfluorene ones allows the synthesis of new, spectrally stable, fluorene-based copolymers. [source] Some methodological problems concerning nonisothermal kinetic analysis of heterogeneous solid,gas reactionsINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 10 2001P. Budrugeac Isoconversional methods, those using only one curve , = ,(T) (, is the conversion degree and T is the temperature), and invariant kinetic parameter method were applied to estimate the kinetic parameters from the following nonisothermal data: (1) simulated TG curves for a single reaction; (2) TG curves for thermal degradation of PVC; and (3) TG curves for the dehydration of CaC2O4·H2O. The results obtained by applying various methods for the same system are compared and discussed. Finally, a procedure of kinetic analysis is suggested. Its application could lead to kinetic parameter values that can be used to predict either , = ,(t) curves for other heating rates or , = ,(T) curves for isothermal conditions. © 2001 John Wiley & Sons, Inc. Int J chem Kinet 33: 564,573, 2001 [source] A Hibiscus Abelmoschus seed extract as a protective active ingredient to favour FGF-2 activity in skinINTERNATIONAL JOURNAL OF COSMETIC SCIENCE, Issue 6 2009D. Rival Synopsis In the skin, heparin, heparan sulphate and heparan sulphate proteoglycans control the storage and release of growth factors and protect them from early degradation. We developed a cosmetic active ingredient containing Hibiscus Abelmoschus seed extract (trade name LinefactorÔ) that can maintain the FGF-2 content in the skin by mimicking the protective effect of heparan sulphate proteoglycans. By preventing the natural degradation of FGF-2, Hibiscus Abelmoschus seed extract maintains the bioavailability of this growth factor for its target cells, i.e. skin fibroblasts. Our in vitro evaluations showed that this ingredient exhibited heparan sulphate-like properties and dose-dependently protected FGF-2 from thermal degradation. We could also show that, in turn, the protected FGF-2 could stimulate the synthesis of sulphated GAGs, the natural protective molecules for FGF-2, thus providing a double protection. Finally, the in vitro results were confirmed in vivo thanks to a clinical study in which skin biomechanical properties and reduction in wrinkles were assessed. Résumé Dans la peau, l'héparane sulfate et les protéoglycanes à héparane sulfate contrôlent le stockage et la libération des facteurs de croissance et les protègent de la dégradation prématurée. Nous avons développé un actif cosmétique contenant un extrait de graines d'Hibiscus Abelmoschus capable de maintenir le contenu en FGF-2 de la peau en mimant l'effet protecteur des protéoglycanes à héparane sulfate. En prévenant la dégradation naturelle du FGF-2, l'extrait de graines d'Hibiscus Abelmoschus maintient la biodisponibilité de ce facteur de croissance pour ses cellules cibles que sont les fibroblastes de la peau. Les évaluations in vitro ont montré que cet ingrédient possédait des propriétés « héparane sulfate-like » et protégeait le FGF-2 de la dégradation thermique de façon dose-dépendante. Nous avons également pu montrer qu'en retour, le FGF-2 protégé pouvait stimuler la synthèse de GAGs sulfatés naturellement protecteurs du FGF-2, offrant ainsi une double protection. Enfin, les résultats in vitro ont été confirmés in vivo par une étude clinique au cours de laquelle les propriétés biomécaniques de la peau ainsi que la réduction des rides ont étéévaluées. [source] Thermal processing of biomass natural fibre wastes by pyrolysisINTERNATIONAL JOURNAL OF ENERGY RESEARCH, Issue 2 2004Anton R. Reed Abstract Waste biomass material in the form of natural fibres used in the production of textile products were examined for their potential to produce activated carbon by physical activation. The five biomass types were hemp, flax, jute, coir and abaca. Each biomass was pyrolysed in a fixed bed reactor and the char characterized. The char was subsequently, activated with steam in a char activation reactor. The surface area and porosity of the derived activated carbon was determined. Surface areas of between 770 and 879 m2 g,1 were achieved. The yield of activated carbon was mostly less than 20 wt% of the original biomass. The five biomass samples were also pyrolysed in a thermogravimetric analyser. The thermal degradation of the biomas samples were discussed in terms of the thermal degradation of the main components of the biomass, cellulose, hemicellulose and lignin. Copyright © 2004 John Wiley & Sons, Ltd. [source] Synchrotron X-ray reflectivity studies of nanoporous organosilicate thin films with low dielectric constantsJOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 2007Weontae Oh Quantitative, non-destructive X-ray reflectivity analysis using synchrotron radiation sources was successfully performed on nanoporous dielectric thin films prepared by thermal processing of blend films of a thermally curable polymethylsilsesquioxane dielectric precursor and a thermally labile triethoxysilyl-terminated six-arm poly(,-caprolactone) porogen in various compositions. In addition, thermogravimetric analysis and transmission electron microscopy analysis were carried out. These measurements provided important structural information about the nanoporous films. The thermal process used in this study was found to cause the porogen molecules to undergo efficiently sacrificial thermal degradation, generating closed, spherical nanopores in the dielectric film. The resultant nanoporous films exhibited a homogeneous, well defined structure with a thin skin layer and low surface roughness. In particular, no skin layer was formed in the porous film imprinted using a porogen loading of 30,wt%. The film porosities ranged from 0 to 33.8% over the porogen loading range of 0,30,wt%. [source] Effect of boron-containing materials on the flammability and thermal degradation of polyamide 6 composites containing melamineJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010Mehmet Do Abstract Three different boron-containing substances,zinc borate (ZnB), borophosphate (BPO4), and a boron- and silicon-containing oligomer (BSi),were used to improve the flame retardancy of melamine in a polyamide 6 (PA-6) matrix. The combustion and thermal degradation characteristics of PA-6 composites were investigated with the limiting oxygen index (LOI), the UL-94 standard, thermogravimetric analysis (TGA)/Fourier transform infrared (FTIR) spectroscopy, and differential scanning calorimetry (DSC). A slight increase was seen in the LOI values of a sample containing BSi (1 wt %). BPO4 at high loadings showed a V0 rating (indicating the best flame retardancy) and slightly lower LOI values in comparison with samples with only melamine. For ZnB and BSi, glassy film and char formation decreased the dripping rate and sublimation of melamine, and this led to low LOIs. According to the TGA,FTIR results, the addition of boron compounds did not change the decomposition product distribution of melamine and PA-6. The addition of boron compounds affected the flame retardancy by physical means. The TGA data showed that boron compounds and melamine reduced the decomposition temperature of PA-6. According to the DSC data, the inclusion of boron compounds increased the onset temperature of sublimation of melamine and also affected the flame retardancy negatively. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] A study of the recycling and stability of flexographic photopolymer platesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2010Cristina C. Cordeiro Abstract Flexographic photopolymer plates have a wide range of commercial applications despite the fact that recycling of such materials is difficult. In consequence, there is a large bulk of leftover material around the world. In this research, the photopolymer plate waste products, identified as styrene-butadiene rubber (SBR)/polyester are blended into common polypropylene (PP) and ethylenevinylacetate (EVA) resins at different loading percentages. PP and EVA are used as the polymer matrix and the recovered styrene-butadiene rubber (SBR) material as the filler. Evaluation of the mechanical, spectroscopic, thermal and chemical properties, as well as morphology, is done by means of scanning electron microscopy (SEM). Mechanical results show that elongation strongly depends on the matrix polymer: the greater the amount of solid-sheet photopolymer (SSP), the smaller the elongation. No specific interactions were detected; however, thermal degradation and transitions were displaced, suggesting some miscibility. More homogeneity is seen for EVA blends, with no significant chemical attack detected. It is possible to reuse these recycled materials in blends with PP and EVA resins. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Morphology, mechanical properties, and thermal stability of poly(L -lactic acid)/poly(butylene succinate- co -adipate)/silicon dioxide compositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2009Ruyin Wang Abstract Poly(butylene succinate- co -adipate) (PBSA) and two types of SiO2 (hydrophilic or hydrophobic) were used to modify poly(L -lactic acid) (PLLA). The mechanical properties, rheological and thermal behavior, phase morphology, and thermal stability of PLLA/PBSA/SiO2 composites were investigated. The impact strength, flexural strength, and modulus of PLLA/PBSA blends increased after the addition of hydrophobic SiO2 without decreasing the elongation at break, and the elongation at break monotonically decreased with increasing hydrophilic SiO2 content. The melt elasticity and viscosity of the PLLA/PBSA blend increased with the addition of SiO2. The hydrophilic SiO2 was encapsulated by the dispersed PBSA phase in the composites, which led to the formation of a core,shell structure, whereas the hydrophobic SiO2 was more uniformly dispersed and mainly located in the PLLA matrix, which was desirable for the optimum reinforcement of the PLLA/PBSA blend. The thermogravimetric analysis results show that the addition of the two types of SiO2 increased the initial decomposition temperature and activation energy and consequently retarded the thermal degradation of PLLA/PBSA. The retardation of degradation was prominent with the addition of hydrophobic SiO2. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Accelerator adsorption onto carbon nanotubes surface affects the vulcanization process of styrene,butadiene rubber compositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2009A. De Falco Abstract The multiwalled carbon nanotubes (MWCNT) filled styrene,butadiene rubber (SBR) composites were prepared by incorporating MWCNT in a SBR/toluene solution and subsequently evaporating the solvent. These composites have shown a significant improvement in Young's modulus and tensile strength with respect to SBR gum without sacrificing high elongation at break. However, this improvement is less than expected at the higher filler content. Then, the influence of low concentrations of MWCNT on the vulcanization process of the SBR composites was studied by means of rheometer torque curves, swelling measurements, differential scanning calorimeter (DSC) analysis, and Fourier transform infrared (FTIR) spectroscopy. Also, their thermal degradation was studied by thermogravimetric analysis (TGA). It has been noticed that MWCNT affects the cure kinetics of SBR gum matrix reducing all parameters, i.e., the total heat rate and order of the reaction, scorch delay, maximum torque, and crosslink density. This effect increases as MWCNT content does, and it was attributed to the adsorption of the accelerator employed in the vulcanization (N -tert-butyl-benzothiazole-2-sulfenamide) onto the MWCNT surface. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Synthesis, characterization, and kinetic of thermal degradation of oligo-2-[(4-bromophenylimino)methyl]phenol and oligomer-metal complexesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2009smet Kaya Abstract Oligo-2-[(4-bromophenylimino)methyl]phenol (OBPIMP) was synthesized from the oxidative polycondensation reaction of 2-[(4-bromophenylimino)methyl]phenol (BPIMP) with air and NaOCl oxidants in an aqueous alkaline medium between 50 and 90°C. The yield of OBPIMP was found to be 67 and 88% for air and NaOCl oxidants, respectively. Their structures were confirmed by elemental and spectral such as IR, ultraviolet,visible spectrophotometer (UV,vis), 1H-NMR, and 13C-NMR analyses. The characterization was made by TG-DTA, size exclusion chromatography, and solubility tests. The resulting complexes were characterized by electronic and IR spectral measurements, elemental analysis, AAS, and thermal studies. According to TG analyses, the weight losses of OBPIMP, and oligomer-metal complexes with Co+2, Ni+2, and Cu+2 ions were found to be 93.04%, 59.80%, 74.23%, and 59.30%, respectively, at 1000°C. Kinetic and thermodynamic parameters of these compounds investigated by Coats-Redfern, MacCallum-Tanner, and van Krevelen methods. The values of the apparent activation energies of thermal decomposition (Ea), the reaction order (n), preexponential factor (A), the entropy change (,S*), enthalpy change (,H*), and free energy change (,G*) obtained by earlier-mentioned methods were all good in agreement with each other. It was found that the thermal stabilities of the complexes follow the order Cu(II) > Co(II) > Ni(II). © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Kinetic study of the thermal degradation of poly(aryl ether ketone)s containing 2,7-naphthalene moietiesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2008Si-Jie Liu Abstract The degradation of poly(aryl ether ketone) containing 2,7-naphthalene moieties was subjected to dynamic and isothermal thermogravimetry in nitrogen and air. The dynamic experiments showed that the initial degradation temperature, temperature for 5% weight loss, and temperature corresponding to the maximum degradation rate of poly(aryl ether ketone) containing 2,7-naphthalene moieties were a little higher than those of poly(ether ether ketone) and almost independent of the 2,7-naphthalene moiety content. The thermal stability of poly(aryl ether ketone) containing 2,7-naphthalene moieties in air was substantially less than that in nitrogen, and the degradation mechanism was more complex. The results obtained under the isothermal conditions were in agreement with the corresponding results obtained in nitrogen and air under the dynamic conditions. In the dynamic experiments, the apparent activation energies for the degradation processes were 240 and 218 kJ/mol in nitrogen and air for the second reaction stage as the heating rate was higher than 5°C/min. In the isothermal experiments, the apparent activation energies for the degradation processes were 222 and 190 kJ/mol in nitrogen and air, respectively. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Adhesion properties and thermal degradation of silicone rubberJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2007Eung-Soo Kim Abstract Silicone rubber is suitable for the thermal insulator of the rocket motors owing to its heat resisting properties as well as its excellent elasticity and restoring force. However, the adhesion properties of the silicone rubber should be improved greatly to be used as the thermal insulator because of its poor adhesiveness coming from the low surface tension. Functional groups were incorporated through copolymerization to the silicone rubber to induce chemical reaction with the functional groups in the propellant/liner components to enhance the adhesion properties. Peeling tests results disclosed that the incorporation of amine groups was the most efficient for the adhesiveness enhancement and that addition of carbon black improved the adhesiveness still more. Stability against thermal degradation of the silicone rubber was examined by measuring the activation energy through the thermogravimetric analysis. The results revealed that the compounding of the Cloisite® clays boosted up the thermal stability of the silicone rubber much more greatly than that of carbon black. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2782,2787, 2007 [source] Fire-resistant effect of nanoclay on intumescent nanocomposite coatingsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2007Zhen-yu Wang Abstract The aim of the study is the development of an intumescent nanocomposite coating to provide fire protection for the metallic substrate. Acrylic nanocomposites containing nanoclay and relative intumescent nanocoatings are prepared. The effect of nanoclay on the thermal degradation of an intumescent nanocomposite coating is analyzed by using differential thermal analysis, thermogravimetry, and X-ray diffraction. The influence of the added content of nanoclay on fire performance is studied by a fire protection test and measurements of the limiting oxygen index and effective thermal conductivity. The distribution of nanoparticles in the acrylic nanocomposite is characterized by transmission electron microscopy. The flame-retardant efficiency of the intumescent nanocomposite coating is improved by 1.5% well-distributed nanoclay particles. However, 3% nanoclay produces a negative effect on the fire performance of the coating. Fire protection tests and scanning electron microscopy observations reveal that the fire-retardant property of a conventional intumescent coating is destroyed by aging, whereas the nanocomposite coating modified with 1.5% nanoclay demonstrates good aging and fire resistance. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 1681,1689, 2007 [source] Development of a 95/5 poly(L -lactide- co -glycolide)/hydroxylapatite and ,-tricalcium phosphate scaffold as bone replacement material via selective laser sinteringJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2008Rebecca Louise Simpson Abstract 95/5 Poly(L -lactide- co -glycolide) was investigated for the role of a porous scaffold, using the selective laser sintering (SLS) fabrication process, with powder sizes of 50,125 and 125,250 ,m. SLS parameters of laser power, laser scan speed, and part bed temperature were altered and the degree of sintering was assessed by scanning electron microscope. Composites of the 125,250 ,-tricalcium phosphate (CAMCERAM® II) were sintered, and SLS settings using 40 wt % CAMCERAM® II were optimized for further tests. Polymer thermal degradation during processing led to a reduction in number and weight averaged molecular weight of 9% and 12%, respectively. Compression tests using the optimized composite sintering parameters gave a Young's modulus, yield strength, and strain at 1% strain offset of 0.13 ± 0.03 GPa, 12.06 ± 2.53 MPa, and 11.39 ± 2.60%, respectively. Porosity was found to be 46.5 ± 1.39%. CT data was used to create an SLS model of a human fourth middle phalanx and a block with designed porosity was fabricated to illustrate the process capabilities. The results have shown that this composite and fabrication method has potential in the fabrication of porous scaffolds for bone tissue engineering. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008 [source] Catalytic conversion of waste plastics: focus on waste PVCJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 9 2007Mark A Keane Abstract Effective waste management must address waste reduction, reuse, recovery/recycling and, as the least progressive option, waste treatment. The increase in plastic waste production is a serious environmental issue. Plastics consumption continues to grow and while plastic recycling has seen a significant increase since the early 1990s, consumption still far exceeds recycling. Waste plastic can, however, serve as a potential resource and, with the correct treatment, can be reused or serve as hydrocarbon raw material or as a fuel. PVC, highly versatile with many applications, is non-biodegradable and has a high Cl content (56% of the total weight). Waste PVC incineration is highly energy demanding and can result in the formation of toxic chloro-emissions with adverse ecological, environmental and public health impacts. The Cl component must be removed from any waste PVC derived gas or oil before it can be used. An overview of the existing waste plastic treatment technologies is provided with an analysis of the available literature on thermal and catalytic PVC degradation. Thermal degradation results in random scissioning of the polymer chains generating products with varying molecular weights and uncontrolled Cl content. There is a dearth of literature dealing with the catalytic dechlorination of PVC. A case study is presented to illustrate the role heterogeneous catalysis can play in PVC waste treatment. The efficacy of Pd/Al2O3 to promote PVC dechlorination is demonstrated, where a significant decrease (by up to a factor of 560) in the liquid fraction Cl content is recorded in addition to differences (relative to thermal degradation) in the gas phase product, i.e. higher C1C4 content with preferential alkane formation. Copyright © 2007 Society of Chemical Industry [source] Pasteurization of Fruit Juices by Means of a Pulsed High Pressure ProcessJOURNAL OF FOOD SCIENCE, Issue 3 2010Giorgio Donsì ABSTRACT:, The use of pulsed high hydrostatic pressure was investigated as a possible approach to stabilize foodstuffs. The objective of this article was to investigate the effect of the main processing variables (pressure [150 to 300 MPa], temperature levels [25 to 50 °C], and pulse number [1 to 10]) on the sanitation of nonpasteurized clear Annurca apple juice as well as freshly-squeezed clear orange juice. The aim of the article was the optimization of the process parameters in step-wise pressure treatment (pressure holding time of each pulse: 60 s, compression rate: 10.5 MPa/s, decompression time: 2 to 5s). The shelf life of the samples, processed at optimized conditions, was evaluated in terms of microbiological stability and quality retention. According to our experimental results, the efficiency of pulsed high pressure processes depends on the combination of pulse holding time and number of pulses. The pulsed high pressure cycles have no additive or synergetic effect on microbial count. The efficacy of the single pulses decreases with the increase of the pulse number and pressure level. Therefore the first pulse cycle is more effective than the following ones. By coupling moderate heating to high pressure, the lethality of the process increases but thermal degradation of the products can be detected. The optimization of the process condition thus results in a compromise between the reduction of the pressure value, due to the synergetic temperature action, and the achievement of quality of the final production. The juices processed under optimal processing conditions show a minimum shelf life of 21 d at a storage temperature of 4 °C. [source] | |||||||||||||||||||||||||||||||