Enhancement of cardanol-loaded halloysite for the thermo-oxidative stability and crystallization property of polylactic acid

2022 ◽  
Vol 216 ◽  
pp. 106357
Author(s):  
Chenyang Li ◽  
Weiguang Gong ◽  
Qiming Cao ◽  
Zhongyang Yao ◽  
Xin Meng ◽  
...  
Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 887
Author(s):  
Meng Wang ◽  
Weiwei Ding ◽  
Yeping Xie ◽  
Lifan Zhang ◽  
Yinghong Chen

Microinjection molding is a novel frontier polymer processing strategy different from conventional ones. In this paper, three different cavity-sizes of micro-mold tools were firstly fabricated, and the influences of micro-mold cavity dimension on the phase morphology structure, crystallization and orientation, and mechanical performance of the microinjection molded polylactic acid (PLA)/polycaprolactone (PCL) blend microparts were carefully investigated accordingly. The results show that the reduction of the cavity size would result in much higher shear stress field and cooling temperature gradient, which is advantageous to the fibrillation and orientation of PCL-dispersed phase. Consequently, with decreasing the micro-mold cavity dimension from length 26 mm to 15 mm, the interfacial compatibility is improved, significantly increasing number of PCL fibers with smaller diameter are in situ formed in PLA matrix and their orientation degree also obviously increases, which is verified by SEM and 2D-WAXD measurements. The Differential Scanning Calorimetry (DSC) analysis shows that the decrease in cavity dimension causes the enhancement of PLA crystallization property due to shear-induced crystallization, which is reflected by the decreasing PLA cold crystallization temperature and increasing PLA crystallinity (almost doubling that of conventional macropart). As a result, the dynamic/static mechanical property measurements exhibit that with decreasing the cavity size, the storage modulus, and the loss modulus of PLA/PCL blend micropart increase, and the corresponding tensile strength, elongation at break, and Young’s modulus also present an obviously increasing tendency. The related investigations would provide some new spaces and insights for realization of high-performance of PLA/PCL blend micropart.


2019 ◽  
Author(s):  
Georg Dewald ◽  
Saneyuki Ohno ◽  
Marvin Kraft ◽  
Raimund Koerver ◽  
Paul Till ◽  
...  

<p>All-solid-state batteries are often expected to replace conventional lithium-ion batteries in the future. However, the practical electrochemical and cycling stability of the best-conducting solid electrolytes, i.e. lithium thiophosphates, are still critical issues that prevent long-term stable high-energy cells. In this study, we use <i>stepwise</i><i>cyclic voltammetry </i>to obtain information on the practical oxidative stability limit of Li<sub>10</sub>GeP<sub>2</sub>S<sub>12</sub>, a Li<sub>2</sub>S‑P<sub>2</sub>S<sub>5</sub>glass, as well as the argyrodite Li<sub>6</sub>PS<sub>5</sub>Cl solid electrolytes. We employ indium metal and carbon black as the counter and working electrode, respectively, the latter to increase the interfacial contact area to the electrolyte as compared to the commonly used planar steel electrodes. Using a stepwise increase in the reversal potentials, the onset potential at 25 °C of oxidative decomposition at the electrode-electrolyte interface is identified. X‑ray photoelectron spectroscopy is used to investigate the oxidation of sulfur(-II) in the thiophosphate polyanions to sulfur(0) as the dominant redox process in all electrolytes tested. Our results suggest that after the formation of these decomposition products, significant redox behavior is observed. This explains previously reported redox activity of thiophosphate solid electrolytes, which contributes to the overall cell performance in solid-state batteries. The <i>stepwise cyclic voltammetry</i>approach presented here shows that the practical oxidative stability at 25 °C of thiophosphate solid electrolytes against carbon is kinetically higher than predicted by thermodynamic calculations. The method serves as an efficient guideline for the determination of practical, kinetic stability limits of solid electrolytes. </p>


2019 ◽  
Author(s):  
Georg Dewald ◽  
Saneyuki Ohno ◽  
Marvin Kraft ◽  
Raimund Koerver ◽  
Paul Till ◽  
...  

<p>All-solid-state batteries are often expected to replace conventional lithium-ion batteries in the future. However, the practical electrochemical and cycling stability of the best-conducting solid electrolytes, i.e. lithium thiophosphates, are still critical issues that prevent long-term stable high-energy cells. In this study, we use <i>stepwise</i><i>cyclic voltammetry </i>to obtain information on the practical oxidative stability limit of Li<sub>10</sub>GeP<sub>2</sub>S<sub>12</sub>, a Li<sub>2</sub>S‑P<sub>2</sub>S<sub>5</sub>glass, as well as the argyrodite Li<sub>6</sub>PS<sub>5</sub>Cl solid electrolytes. We employ indium metal and carbon black as the counter and working electrode, respectively, the latter to increase the interfacial contact area to the electrolyte as compared to the commonly used planar steel electrodes. Using a stepwise increase in the reversal potentials, the onset potential at 25 °C of oxidative decomposition at the electrode-electrolyte interface is identified. X‑ray photoelectron spectroscopy is used to investigate the oxidation of sulfur(-II) in the thiophosphate polyanions to sulfur(0) as the dominant redox process in all electrolytes tested. Our results suggest that after the formation of these decomposition products, significant redox behavior is observed. This explains previously reported redox activity of thiophosphate solid electrolytes, which contributes to the overall cell performance in solid-state batteries. The <i>stepwise cyclic voltammetry</i>approach presented here shows that the practical oxidative stability at 25 °C of thiophosphate solid electrolytes against carbon is kinetically higher than predicted by thermodynamic calculations. The method serves as an efficient guideline for the determination of practical, kinetic stability limits of solid electrolytes. </p>


Author(s):  
Nobuyuki Kawashima ◽  
Shinji Ogawa ◽  
Shoji Obuchi ◽  
Mitsunori Matsuo ◽  
Tadashi Yagi
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