Effects of Microcrystalline Cellulose on the Thermal Properties of Poly(3-hydroxybutyrate-co-3-hydroxyvalerate)

2011 ◽  
Vol 284-286 ◽  
pp. 1778-1781 ◽  
Author(s):  
Zhe Zhou ◽  
Hou Yong Yu ◽  
Mei Fang Zhu ◽  
Zong Yi Qin
Keyword(s):  
Thermal Stability ◽  
Thermal Properties ◽  
Microcrystalline Cellulose ◽  
Crystallization Temperature ◽  
Solvent Casting ◽  
Melt Crystallization ◽  
Casting Method ◽  
Nucleation Agent ◽  
Tga And Dsc ◽  
Thermal Stability Of

The composites of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) with different microcrystalline cellulose (MCC) contents were prepared by a solvent casting method. The effects of MCC on the thermal properties of PHBV were studied by TGA and DSC. The DSC results showed that the melt crystallization temperature of the PHBV/MCC increased from 41.9 °C for PHBV to 59.8 °C for the composites containing 20 wt. % MCC, which indicated that the crystallization of PHBV became easier with the addition of MCC. It also illustrated that the MCC could be used as an effective nucleation agent for the crystallization of PHBV. Moreover, it was found that the thermal stability of the PHBV/MCC composites increased compared with the neat PHBV.

Effect of Cellulose Nanocrystal on Crystallization Behavior of Poly(3–hydroxybutyrate–co–3–hydroxyvalerate)

2012 ◽  
Vol 430-432 ◽  
pp. 20-23 ◽  
Author(s):  
Hou Yong Yu ◽  
Zong Yi Qin
Keyword(s):  
Heterogeneous Nucleation ◽  
Crystallization Temperature ◽  
Crystallization Behavior ◽  
Crystallization Rate ◽  
Kinetics Study ◽  
Solvent Casting ◽  
Melt Crystallization ◽  
Casting Method ◽  
Isothermal Crystallization Kinetics ◽  
Biodegradable Nanocomposites

The biodegradable nanocomposites of poly (3–hydroxybutyrate–co–3–hydroxyvalerate) (PHBV) with different cellulose nanocrystals (CNCs) contents were prepared by a solvent casting method. The effects of CNCs on the crystallization behavior of PHBV were studied by DSC. The DSC results showed that compared to PHBV, the melt crystallization temperature increased to 92.3 °C for the nanocomposites with 10 wt. % CNCs, which indicated that the crystallization of PHBV became easier with the addition of CNCs. Moreover, the non–isothermal crystallization kinetics study illustrated that overall crystallization rate of PHBV in the nanocomposites was faster than that of neat PHBV, which should be attributed to the strong heterogeneous nucleation of CNCs.

scholarly journals Preparation and characterization of polyhedral oligomeric silsesquioxane/polystyrene nanocomposites

e-Polymers ◽  
2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Benhong Yang ◽  
Meng Li ◽  
Yun Wu ◽  
Kang Wang
Keyword(s):  
Thermal Stability ◽  
Thermal Property ◽  
Polyhedral Oligomeric Silsesquioxane ◽  
29Si Nmr ◽  
Solution Blending ◽  
Oligomeric Silsesquioxane ◽  
Tga And Dsc ◽  
Thermal Stability Of

AbstractSeveral inorganic/organic nanocomposites were prepared via solution-blending of cage-like octahexyl-polyhedral oligomeric silsesquioxane (Oh-POSS) with polystyrene (PS) in THF solvent. FTIR and 29Si-NMR were employed to characterize the structures of the nanocomposites. SEM pictures showed that the sample films were smooth and no POSS aggregation was observed when POSS content was lower than 1.0 wt%. TGA and DSC were used to investigate the thermal property. The results showed that the incorporation of nanosized Oh-POSS enhanced the thermal stability of PS with low POSS content. When 1.0 wt% of Oh-POSS was incorporated into PS matrix, the Tg and Td increased by 7.7 °C and 8.2 °C, respectively. However, higher POSS contents (>1.0 wt%) would deteriorate the thermal property of the nanocomposites due to the severe congregation of POSS..

Preparation and Thermal Properties of High-Purified Molten Nitrate Salt Materials with Heat Transfer and Storage

2015 ◽  
Vol 34 (8) ◽  
Author(s):  
Hongtao Zhang ◽  
Youjing Zhao ◽  
Jingli Li ◽  
Lijie Shi ◽  
Min Wang
Keyword(s):  
Heat Transfer ◽  
Thermal Stability ◽  
Thermal Properties ◽  
Molten Salts ◽  
Operating Temperature ◽  
Nitrate Salt ◽  
Solar Salt ◽  
And Storage ◽  
Thermal Stability Of ◽  
Operating Temperature Range

AbstractThis paper focuses on thermal stability of molten salts, operating temperature range and latent heat of molten salts at a high temperature. In this experiment, multi-component molten salts (purified Solar Salt) composed of purified NaNO

scholarly journals The Thermal Properties of Polyurethane/Neoprene Blends on Prosthetic Foot

2020 ◽  
Vol 990 ◽  
pp. 106-110
Author(s):  
Mohd Zulkifli Mohamad Noor ◽  
Mohamad Anas Mohd Azmi ◽  
Mohd Shaiful Zaidi Mad Desa ◽  
Mohd Bijarimi Mat Piah ◽  
Azizan Ramli
Keyword(s):  
Thermal Stability ◽  
Thermal Properties ◽  
Low Cost ◽  
Decomposition Temperature ◽  
Gravimetric Analysis ◽  
Thermal Gravimetric ◽  
Prosthetic Foot ◽  
Reinforced Polymer ◽  
New Material ◽  
Thermal Stability Of

Neoprene reinforced polymer has become an attraction in current research and development of new material blend. In this invention, neoprene was chosen to be enhance to polyurethane because of their superior properties that possess extraordinary mechanical, electrical, optical and thermal properties on prosthetic foot. In this research, polyurethane was chosen due to good rigidity, easy processing and low cost. The reinforcement polyurethane with neoprene is expected to improve the properties of polyurethane. The objective of this research was conducted to investigate the effect of neoprene contents on thermal properties of polyurethane reinforced neoprene on prosthetic foot. The effect of neoprene on thermal properties neoprene reinforced polyurethane was analysed in term of its thermal stability by thermal gravimetric analysis (TGA). Moreover, the visual of small topographic details on the surface of polyurethane/neoprene blends will be examined by scanning electron microscope (SEM). Based on result, the thermal properties show the great enhancement at high neoprene contents which is 1.0wt%. The thermal stability of polyurethane reinforced neoprene improves when the temperature where decomposition starts to occurs are higher than decomposition temperature of pure polyurethane. Then, thermal conductivity of polyurethane shows the great improvement after the addition of neoprene. Lastly, the smooth surface and visible of sheets pattern on surface represent the present of neoprene disperse into polymer that enhance brittleness. Thus, the presence of neoprene has clearly enhanced the thermal stability of the polyurethane. Table 1 shows formulation of neoprene and polyurethane.

Effect of Phenylene Diamine Antioxidant on Physico-Chemical Properties of Methyl Grafted Natural Rubber Polymer Electrolytes

2017 ◽  
Vol 864 ◽  
pp. 48-53
Author(s):  
Ahmad Fairoz Aziz ◽  
Khuzaimah Nazir ◽  
S.F. Ayub ◽  
N.I. Adam ◽  
Muhd Zu Azhan Yahya ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Natural Rubber ◽  
Polymer Electrolytes ◽  
Chemical Properties ◽  
Physico Chemical ◽  
Solution Cast ◽  
Deconvolution Techniques ◽  
Tga And Dsc ◽  
Thermal Stability Of ◽  
Aging Factor

0.5 wt.% of N-(1,3-dimethylbutyl)-N’-phenyl-p-phenylenediamine (6PPD) was introduced into polymer electrolytes based on 30% poly(methyl-methacrylate) grafted natural rubber (MG30) in order to reduce the aging factor of MG30. The polymer electrolyte without 6PPD was used as control. All samples were prepared by using solution cast techniques. The effect of 6PPD in the electrolytes was analysed by using TGA, DSC and FTIR. TGA and DSC results revealed the thermal stability of MG30 electrolytes with 6PPD have higher thermal stability but lower glass transition temperature value. FTIR studies confirmed the existence of LiTF in the sample and prove the occurrence of polymer-salt complexation. Deconvolution techniques analysis on FTIR spectra shows the electrolyte sample with 6PPD display more ion dissociation which reflects to higher ionic conductivity.

Epoxy Cured with Anhydride Terminated Polydimethylsiloxane: Cure Kinetics and Thermal Properties

2011 ◽  
Vol 415-417 ◽  
pp. 261-264
Author(s):  
Yuan Ren ◽  
Zheng Xi ◽  
Wen Jun Gan ◽  
Liang Zhang ◽  
Jing Zhang ◽  
...  
Keyword(s):  
Activation Energy ◽  
Thermal Stability ◽  
Thermal Properties ◽  
Succinic Anhydride ◽  
Cure Kinetics ◽  
Diglycidyl Ether ◽  
Scanning Calorimetry ◽  
Thermogravimetric Analyses ◽  
Isothermal Measurements ◽  
Thermal Stability Of

A siloxane-containing dianhydride, succinic anhydride terminated polydimethylsiloxane (DMS-Z21) was selected to cure diglycidyl ether of bisphenol-A based epoxy resin (DGEBA). The cure kinetics and thermal properties were investigated by nonisothermal and isothermal differential scanning calorimetry (DSC) and thermogravimetric analyses (TGA), respectively. The activation energy (Ea) of the curing reaction was obtained based on the methods of Kissinger and isothermal measurements. The results of the thermogravimetric analyses of the DGEBA/DMS-Z21 system showed that the thermal stability of the DGEBA/DMS-Z21 system was slightly higher than the DGEBA/MeTHPA system.

Morphology, Mechanical and Thermal Properties of Poly(Lactic Acid)/Propylene-Ethylene Copolymer/Cellulose Composites

2019 ◽  
Vol 972 ◽  
pp. 172-177
Author(s):  
Sirirat Wacharawichanant ◽  
Patteera Opasakornwong ◽  
Ratchadakorn Poohoi ◽  
Manop Phankokkruad
Keyword(s):  
Thermal Stability ◽  
Lactic Acid ◽  
Thermal Properties ◽  
Tensile Stress ◽  
Cellulose Fibers ◽  
Phase Morphology ◽  
Poly Lactic Acid ◽  
Mechanical And Thermal Properties ◽  
Ethylene Copolymer ◽  
Thermal Stability Of

This work studied the effects of various types of cellulose fibers on the morphology, mechanical and thermal properties of poly(lactic acid) (PLA)/propylene-ethylene copolymer (PEC) (90/10 w/w) blends. The PLA/PEC blends before and after adding cellulose fibers were prepared by melt blending method in the internal mixer and molded by compression method. The morphological analysis observed that the presence of cellulose in PLA did not change the phase morphology of PLA, and PLA/cellulose composite surfaces were observed the cellulose fibers inserted in PLA matrix and fiber pull-out. The phase morphology of PLA/PEC blends was changed from brittle fracture to ductile fracture behavior and showed the phase separation between PLA and PEC phases. The presence of celluloses did not improve the compatibility between PLA and PEC phases. The tensile stress and strain curves found that the tensile stress of PLA was the highest value. The addition of all celluloses increased Young’s modulus of PLA. The PEC presence increased the tensile strain of PLA over two times when compared with neat PLA and PLA was toughened by PEC. The incorporation of cellulose fibers in PLA/PEC blends could improve Young’s modulus, tensile strength, and stress at break of the blends. The thermal stability showed that the degradation temperatures of all types of cellulose were less than the degradation temperatures of PLA. Thus, the incorporation of cellulose in PLA could not enhance the thermal stability of PLA composites and PLA/PEC composites. The degradation temperature of PEC was the highest value, but it could not improve the thermal stability of PLA. The incorporation of cellulose fibers had no effect on the melting temperature of the PLA blend and composites.

Mechanical and thermal properties of polyoxymethylene-matrix composites filled with multi-walled carbon nanotubes-coated milled glass fiber

2019 ◽  
Vol 54 (15) ◽  
pp. 1961-1976
Author(s):  
Xu Xiangmin ◽  
Hongxiang Zhang ◽  
Tong Beibei ◽  
Li Binjie ◽  
Yudong Zhang
Keyword(s):  
Carbon Nanotubes ◽  
Thermal Stability ◽  
Thermal Properties ◽  
Electron Microscope ◽  
Glass Fiber ◽  
Crystallization Temperature ◽  
High Performance ◽  
Multiwall Carbon Nanotubes ◽  
Fiber Surface ◽  
Mechanical And Thermal Properties

The advanced multifunctional filler has become one of the main challenges in developing high-performance polymer composites. In this study, the acid-treated multiwall carbon nanotubes (MWCNTs) were adhered to the surface of milled glass fiber under the combined effect of 3-aminopropyltriethyloxy silane and tetraethyl orthosilicate to fabricate a hierarchical fiber (MWCNTs-MGF). The morphologies of the hierarchical fibers were characterized using field-emission scanning electron microscope and transmission electron microscope, which showed evidence of a coating layer of MWCNTs on each fiber surface. The MWCNTs-MGF was employed as a multifunctional filler to prepare polyoxymethylene-based composites using a twin-screw extruder by melt blending. The obtained composites exhibited improved mechanical and thermal properties. The composite tensile strength and notched impact strength and Young's modulus increased by 10%, 32%, and 32%, respectively, as the MWCNTs-MGF content varies from 0 to 10 wt.%. Meanwhile, the reinforcing and toughing mechanisms of MWCNTs-MGF were also elaborated by analyzing the interfacial adhesion and fracture morphologies of the composites. Moreover, the study on thermal stability and crystallization behavior indicated that the polyoxymethylene/MWCNTs-MGF composites had higher thermal stability, crystallization temperature, and crystallinity as compared to the polymer matrix. The improvement of thermal stability originates from the unique surface structure of MWCNTs-MGF, while the increase in crystallization temperature and crystallinity is due to the strong heterogeneous nucleation ability of the hierarchical fibers.

Crystallization Behaviours of Poly(vinylidene fluoride) (PVDF) Nanocomposites with MoS2 Nanosheets with Different Surface Functional Groups

2020 ◽  
Vol 20 (12) ◽  
pp. 7535-7543
Author(s):  
Guihai Gan ◽  
Cheng Wang ◽  
Pengpeng Chen ◽  
Jichang Liu
Keyword(s):  
Thermal Stability ◽  
Crystallization Temperature ◽  
Vinylidene Fluoride ◽  
Crystallization Rate ◽  
Cold Crystallization ◽  
Degree Of Crystallinity ◽  
Mos2 Nanosheets ◽  
Surface Functional Groups ◽  
Poly Vinylidene Fluoride ◽  
Thermal Stability Of

The crystallization behaviours of amorphous poly(vinylidene fluoride) (PVDF) nanocompositesmodified with two different kinds of molybdenum disulfide (MoS2) at different filler loadings were investigated in detail in this work. The crystallinity, melting temperature and crystallization temperature of the PVDF/MoS2 nanocomposites were transformed from α-phase to β-phase with the addition of MoS2, MoS2-COOH and MoS2-NH2. During isothermal cold crystallization, the overall crystallization rate of PVDF was slowed with increased MoS2 loading relative to that of neat PVDF. Moreover, the crystallization temperature of the PVDF nanocomposites increased with the addition of MoS2 despite the cooling rate during nonisothermal cold crystallization. DMA tests showed that the storage modulus of PVDF was decreased with the addition of MoS2, while those of PVDF/MoS2-COOH and PVDF/MoS2-NH2 were enhanced to different degrees. The decomposition of the PVDF/MoS2 nanocomposites were also discussed. Relative to neat PVDF, the thermal stability of PVDF was obviously improved with the addition of MoS2, MoS2-COOH and MoS2-NH2, which could be ascribed to the increased degree of crystallinity.

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