scholarly journals Crystallization behavior and thermal stability of poly(butylene succinate)/poly(propylene carbonate) blends prepared by novel vane extruder

2016 ◽  
Author(s):  
Rongyuan Chen ◽  
Wei Zou ◽  
Haichen Zhang ◽  
Guizhen Zhang ◽  
Jinping Qu
Keyword(s):  
Thermal Stability ◽  
Propylene Carbonate ◽  
Crystallization Behavior ◽  
Butylene Succinate ◽  
Poly Propylene ◽  
Thermal Stability Of

scholarly journals Study on Thermal Decomposition Behaviors of Terpolymers of Carbon Dioxide, Propylene Oxide, and Cyclohexene Oxide

2018 ◽  
Vol 19 (12) ◽  
pp. 3723 ◽  
Author(s):  
Shaoyun Chen ◽  
Min Xiao ◽  
Luyi Sun ◽  
Yuezhong Meng
Keyword(s):  
Carbon Dioxide ◽  
Thermal Stability ◽  
Thermal Decomposition ◽  
Thermogravimetric Analysis ◽  
Propylene Carbonate ◽  
Cyclohexene Oxide ◽  
Block Polymers ◽  
Rate Method ◽  
Poly Propylene ◽  
Thermal Stability Of

The terpolymerization of carbon dioxide (CO2), propylene oxide (PO), and cyclohexene oxide (CHO) were performed by both random polymerization and block polymerization to synthesize the random poly (propylene cyclohexene carbonate) (PPCHC), di-block polymers of poly (propylene carbonate–cyclohexyl carbonate) (PPC-PCHC), and tri-block polymers of poly (cyclohexyl carbonate–propylene carbonate–cyclohexyl carbonate) (PCHC-PPC-PCHC). The kinetics of the thermal degradation of the terpolymers was investigated by the multiple heating rate method (Kissinger-Akahira-Sunose (KAS) method), the single heating rate method (Coats-Redfern method), and the Isoconversional kinetic analysis method proposed by Vyazovkin with the data from thermogravimetric analysis under dynamic conditions. The values of ln k vs. T−1 for the thermal decomposition of four polymers demonstrate the thermal stability of PPC and PPC-PCHC are poorer than PPCHC and PCHC-PPC-PCHC. In addition, for PPCHC and PCHC-PPC-PCHC, there is an intersection between the two rate constant lines, which means that, for thermal stability of PPCHC, it is more stable than PCHC-PPC-PCHC at the temperature less than 309 °C and less stable when the decomposed temperature is more than 309 °C. Pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) and thermogravimetric analysis/infrared spectrometry (TG/FTIR) techniques were applied to investigate the thermal degradation behavior of the polymers. The results showed that unzipping was the main degradation mechanism of all polymers so the final pyrolysates were cyclic propylene carbonate and cyclic cyclohexene carbonate. For the block copolymers, the main chain scission reaction first occurs at PC-PC linkages initiating an unzipping reaction of PPC chain and then, at CHC–CHC linkages, initiating an unzipping reaction of the PCHC chain. That is why the T−5% of di-block and tri-block polymers were not much higher than that of PPC while two maximum decomposition temperatures were observed for both the block copolymer and the second one were much higher than that of PPC. For PPCHC, the random arranged bulky cyclohexane groups in the polymer chain can effectively suppress the backbiting process and retard the unzipping reaction. Thus, it exhibited much higher T−5% than that of PPC and block copolymers.

A novel method to improve the thermal stability of poly(propylene carbonate)

2014 ◽  
Vol 5 (14) ◽  
pp. 4245-4250 ◽  
Author(s):  
Jingjing An ◽  
Yucai Ke ◽  
Xinyu Cao ◽  
Yongmei Ma ◽  
Fosong Wang
Keyword(s):  
Thermal Stability ◽  
Propylene Carbonate ◽  
Melt Blending ◽  
Biodegradable Material ◽  
New Finding ◽  
Novel Method ◽  
Poly Propylene ◽  
Thermal Stability Of

The introduction of NP-10P by simple melt-blending can significantly improve the thermal stability of PPC. This new finding will facilitate development and widespread applications of this biodegradable material.

Preparation and Characterization of Poly(propylene carbonate)/Alkali Lignin Composite Sheets by Calendering Process

2011 ◽  
Vol 233-235 ◽  
pp. 1786-1789 ◽  
Author(s):  
Li Sha Pan ◽  
Nai Xu ◽  
Zheng Tian ◽  
Ling Bin Lu ◽  
Su Juan Pang ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Thermal Stability ◽  
Propylene Carbonate ◽  
Convenient Method ◽  
Interfacial Interaction ◽  
Alkali Lignin ◽  
Aliphatic Polycarbonate ◽  
Poly Propylene ◽  
Thermal Stability Of

PPC is a new biodegradable aliphatic polycarbonate with poor thermal stability and mechanical properties which is difficult to form sheets or films and so on. Through the addition of alkali lignin, thermal stability and mechanical properties of PPC was improved largely. PPC/ alkali lignin sheets could be prepared. DSC results showed that the thermal stability of PPC was improved by the introduction of alkali lignin. SEM showed good dispersion of alkali lignin particles into PPC matrix that resulted in good miscibility. Improved mechanical properties and thermal stability of PPC/ alkali lignin blends were attributed to stronger interfacial interaction of PPC and alkali lignin. These results indicate that blending PPC with alkali lignin is an efficient and convenient method to improve the properties of PPC.

scholarly journals Effect of exchange reactions and free radical grafting on the high‐speed reactive extrusion of poly(butylene succinate) and poly(propylene carbonate) blends

2019 ◽  
Vol 59 (10) ◽  
pp. 1986-1998
Author(s):  
Bárbara A. Calderón ◽  
Conor W. Thompson ◽  
Vincenzo L. Barinelli ◽  
Matthew S. McCaughey ◽  
Margaret J. Sobkowicz
Keyword(s):  
Free Radical ◽  
Propylene Carbonate ◽  
High Speed ◽  
Reactive Extrusion ◽  
Exchange Reactions ◽  
Butylene Succinate ◽  
Poly Propylene

Thermal stability, crystallization and mechanical properties of nylon11/montmorillonite nanocomposites

e-Polymers ◽  
2011 ◽  
Vol 11 (1) ◽  
Author(s):  
Yingchun Li ◽  
Guosheng Hu ◽  
Bin He
Keyword(s):  
Thermal Stability ◽  
Tensile Strength ◽  
Crystallization Behavior ◽  
Nucleating Agent ◽  
Avrami Equation ◽  
Melt Compounding ◽  
Izod Impact ◽  
Nylon 11 ◽  
Thermal Stability Of ◽  
Montmorillonite Nanocomposites

AbstractNylon 11 nanocomposites with different montmorillonite loadings were successfully prepared by melt compounding. XRD and TEM show the exfoliated nanocomposites are formed at low montmorillonite concentration (less than 2 wt%) and the intercalated nanocomposites are obtained at higher montmorillonite contents. TGA shows that the thermal stability of the nanocomposites is improved by 27 °C when the montmorillonite content is only 2wt%. At the same time, The crystallization behavior of nylon11/montmorillonite nanocomposites has been studied by means of XRD, DSC.The Avrami equation described well the isothermal crystallization behavior of nylon11 and nylon11/montmorillonite nanocomposites. The results showed that the montmorillonite acted as the nucleating agent and facilitated the crystal growth rate of nylon 11 matrix. The incorporation of montmorillonite did not change the crystal morphology of nylon 11 but increased the crystallization temperature and decreased the crystallization activation energy, which lead to a easy crystallization of nylon11. Mechanical testing shows that the Izod impact strength of all nanocomposites are higher than that of the neat nylon 11, but the tensile strength of the nanocomposites decrease at low nanofiller concentrations (less than 8wt%) and then increased, when the montmorillonite content is 10wt% ,the tensile strength of the nanocomposite is 5% improved than neat nylon 11. This is may be due to the strong interaction between the nylon 11 matrix and the montmorillonite interface.

Thermal and Thermomechanical Properties of Poly(butylene succinate) Nanocomposites

2008 ◽  
Vol 8 (4) ◽  
pp. 1679-1689 ◽  
Author(s):  
Mamookho E. Makhatha ◽  
Suprakas Sinha Ray ◽  
Joseph Hato ◽  
Adriaan S. Luyt
Keyword(s):  
Thermal Stability ◽  
Tensile Modulus ◽  
Melting Behavior ◽  
Mechanical Analysis ◽  
Thermomechanical Properties ◽  
Scanning Calorimetry ◽  
Melt Mixing ◽  
Butylene Succinate ◽  
Modulated Differential Scanning Calorimetry ◽  
Thermal Stability Of

This article describes the thermal and thermomechanical properties of poly(butylene succinate) (PBS) and its nanocomposites. PBS nanocomposites with three different weight ratios of organically modified synthetic fluorine mica (OMSFM) have been prepared by melt-mixing in a batch mixer at 140 °C. The structure and morphology of the nanocomposites were characterized by X-ray diffraction (XRD) analyses and transmission electron microscopy (TEM) observations that reveal the homogeneous dispersion of the intercalated silicate layers into the PBS matrix. The thermal properties of pure PBS and the nanocomposite samples were studied by both conventional and temperature modulated differential scanning calorimetry (DSC) analyses, which show multiple melting behavior of the PBS matrix. The investigation of the thermomechanical properties was performed by dynamic mechanical analysis. Results reveal significant improvement in the storage modulus of neat PBS upon addition of OMSFM. The tensile modulus of neat PBS is also increased substantially with the addition of OMSFM, however, the strength at yield and elongation at break of neat PBS systematically decreases with the loading of OMSFM. The thermal stability of the nanocomposites compared to that of the pure polymer sample was examined under both pyrolytic and thermooxidative environments. It is shown that the thermal stability of PBS is increased moderately in the presence of 3 wt% of OMSFM, but there is no significant effect on further silicate loading in the oxidative environment. In the nitrogen environment, however, the thermal stability systematically decreases with increasing clay loading.

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