scholarly journals Effects of Boric Acid Ester Modified Magnesium Borate Whisker on the Mechanical Properties and Crystallization Kinetics of Polypropylene Composites

Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1698 ◽  
Author(s):  
Jin-Hua Luo ◽  
Shi-Hu Han ◽  
Juan Wang ◽  
Hui Liu ◽  
Xiao-Dong Zhu ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Boric Acid ◽  
Isothermal Crystallization ◽  
Acid Ester ◽  
Crystallization Rate ◽  
Scanning Calorimetry ◽  
Magnesium Borate ◽  
Crystallization Property ◽  
Polypropylene Composites ◽  
Boric Acid Ester

Polypropylene (PP) is notch sensitive and brittle under severe conditions of deformation, limiting wider range of its usage as a structural load-bearing polymer. Hence, in this work the magnesium borate whisker (MBw), with similar mechanical properties to carbon fiber but much less expensive than polycrystalline silicon carbide, was modified by boric acid ester (BAE) and then used to fabricate PP composites. The mechanical properties, morphology, and non-isothermal crystallization property of virgin PP, PP/MBw, and PP/BAE-MBw composites were studied through mechanical testing, scanning electron microscopy (SEM), and differential scanning calorimetry (DSC), respectively. The non-isothermal crystallization data was analyzed via Mo, Kissinger, and Dobreva methods. The results reveal that the incorporation of BAE-MBw into PP matrix results in higher tensile strength and impact strength than those of virgin PP and PP/MBw composite. The activation energies based on Kissinger were 190.20 kJ/mol for virgin PP, 206.59 kJ/mol for PP/MBw, and 218.98 kJ/mol for PP/BAE-MBw. The nucleation activities of whiskers determined by the Dobreva model were 0.86 for PP/MBw and 0.75 for PP/BAE-MBw. As a result, the whiskers, especially the modified whiskers, act as active substrates to facilitate heterogeneous nucleation, which leads to an increase in crystallization rate.

Synergistic effects of intumescent flame retardant and nano-CaCO3 on foamability and flame-retardant property of polypropylene composites foams

2017 ◽  
Vol 54 (3) ◽  
pp. 615-631 ◽  
Author(s):  
Li Depeng ◽  
Li Chixiang ◽  
Jiang Xiulei ◽  
Liu Tao ◽  
Zhao Ling
Keyword(s):  
Mechanical Properties ◽  
Stress Concentration ◽  
Flame Retardant ◽  
Synergistic Effects ◽  
Crystallization Rate ◽  
Intumescent Flame Retardant ◽  
Limit Oxygen Index ◽  
Scanning Calorimetry ◽  
Polypropylene Composites ◽  
Flame Retardant Property

Synergistic effects of intumescent flame retardant and nano-CaCO3 on foamability and flame retardant property of polypropylene composites and their foams were carefully investigated. The differential scanning calorimetry results showed that the intumescent flame retardant played a plasticizing effect on the polypropylene/intumescent flame-retardant composites and accelerated the crystallization rate. The rheological properties and supercritical CO2-assisted molding foaming behaviors of the polypropylene/intumescent flame retardant/nano-CaCO3 composites showed that the nano-CaCO3 could enhance their foamability. Scanning electron microscopy pictures and mechanical properties of the polypropylene/intumescent flame-retardant composites foams indicated that the agglomeration of intumescent flame retardant would reduce the cell uniformity and even cause the cell collapse. Furthermore, the stress concentration, caused by the agglomeration, could reduce the mechanical properties of the PP composites foams. The synergistic effect of the nano-CaCO3 could improve the cell uniformity and reduce the stress concentration so that the mechanical properties of the polypropylene/intumescent flame retardant /nano-CaCO3 composites foams were improved. Moreover, the polypropylene/intumescent flame retardant/nano-CaCO3 composites foams had the higher limit oxygen index values than the polypropylene/intumescent flame-retardant foams. TGA results also showed that the nano-CaCO3 could improve the thermal stability of the polypropylene composites foams by forming compact carbon layer. The experimental results indicated that the foamability of the polypropylene composites and the flame-retardant property of their foams could be improved by the synergistic effects of intumescent flame retardant and nano-CaCO3.

The influence of bamboo fiber content on the non-isothermal crystallization kinetics of bamboo fiber-reinforced polypropylene composites (BPCs)

Holzforschung ◽  
2018 ◽  
Vol 72 (4) ◽  
pp. 329-336 ◽  
Author(s):  
Chin-Yin Hsu ◽  
Teng-Chun Yang ◽  
Tung-Lin Wu ◽  
Ke-Chang Hung ◽  
Jyh-Horng Wu
Keyword(s):  
Isothermal Crystallization ◽  
Crystallization Rate ◽  
Bamboo Fiber ◽  
Nucleation Agent ◽  
Scanning Calorimetry ◽  
Relative Crystallinity ◽  
Crystallinity Degree ◽  
Polypropylene Composites ◽  
Time Period ◽  
Crystal Growth Mechanism

AbstractBamboo fiber (BF)-reinforced polypropylene (PP) composites (BPCs) have been investigated and it was shown by differential scanning calorimetry (DSC) that BF is a nucleation agent and accelerates the crystallization rate of the PP matrix. Numerical analyses according to Avrami, Avrami-Ozawa, and Friedman described well the nucleation mechanism, the crystallization rate and the activation energy for the non-isothermal crystallization behavior of BPCs, respectively. The Avrami approach indicated that BF as a reinforcement significantly changed the crystal growth mechanism of PP matrix during the cooling process. Based on the Avrami-Ozawa method, a lower cooling rate can achieve a certain relative crystallinity degree within a time period. According to the Friedman method, the activation energies of BPCs were lower than that of neat PP below a relative crystallinity of 35%, when the BF content was more than 60%.

A New Type of Compatilizer and its Application in Polystyrene Ether/Nylon 66 Alloy

2012 ◽  
Vol 535-537 ◽  
pp. 2513-2516
Author(s):  
Ya Tong Zhang ◽  
Ying Li ◽  
Li Li ◽  
Xiong Wei Qu
Keyword(s):  
Mechanical Properties ◽  
Electron Microscope ◽  
Boric Acid ◽  
Acid Ester ◽  
Test Method ◽  
Tem Analysis ◽  
Boric Acid Ester ◽  
New Type ◽  
Reactive Compatibilizer ◽  
Scanning Electron

This paper studies the influence of Double (L- diethyl tartrate) boric acid ester (compatibilizer B) on the compatibility between PPO and PA66. Through the mechanical properties, Molau experiment, scanning electron microscope and tem analysis test method, it is proved that Double (L- diethyl tartrate) boric acid ester can be used as a new reactive compatibilizer in PPO/PA66 plastic alloy.

Thermal Behavior, Mechanical Properties and Microstructure of Polypropylene Composites Filled by Calcium Carbonate Whiskers

2012 ◽  
Vol 503-504 ◽  
pp. 494-497
Author(s):  
Zhong Li Jiang ◽  
Qiu Ju Sun ◽  
Yan Ran Zhang ◽  
Lin Li
Keyword(s):  
Mechanical Properties ◽  
Stearic Acid ◽  
Thermal Behavior ◽  
Tensile Testing ◽  
Mass Fraction ◽  
Crystallization Rate ◽  
Scanning Calorimetry ◽  
Elongation At Break ◽  
Polypropylene Composites ◽  
Scanning Electron

CaCO3 whiskers were treated by stearic acid and the surface property of the treated whisker were evaluated by activation index. When the mass fraction of stearic acid was 4.0%, activation exponential increased to 80.0% almost from zero. The composites were prepared by blending with polypropylene and the treated whiskers. The performance of the composites, such as thermal behavior, mechanical properties and microstructure, were analyzed with differential scanning calorimetry, scanning electron microscopy and tensile testing. The results showed that CaCO3 whisker played heterogeneous nucleation to induce crystalline behavior of PP phase in the blends and the crystallization rate of PP phase also increased because of CaCO3 whiskers intervening. Moreover thermo-decomposing temperature and tensile strengths of the blends all increased with increasing whisker content, except a little less than that of pure PP as filling 3.22% CaCO3 whiskers, but the elongation at break increased with increasing whisker content.

The non-isothermal crystallization behavior of polyamide 6 and polyamide 6/HDPE/MAH/L-101 composites

2019 ◽  
Vol 39 (2) ◽  
pp. 124-133 ◽  
Author(s):  
Bingxiao Liu ◽  
Guosheng Hu ◽  
Jingting Zhang ◽  
Zhongqiang Wang
Keyword(s):  
Crystallization Kinetics ◽  
Isothermal Crystallization ◽  
Crystallization Behavior ◽  
Isothermal Condition ◽  
Crystallization Rate ◽  
Polyamide 6 ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Analysis And Design ◽  
Processing Techniques

AbstractStudy of the crystallization kinetics is particularly necessary for the analysis and design of processing operations, especially the non-isothermal crystallization behavior, which is due to the fact that most practical processing techniques are carried out under non-isothermal conditions. The non-isothermal crystallization behaviors of polyamide 6 (PA6) and PA6/high-density polyethylene/maleic anhydride/2,5-dimethyl-2,5-di(tert-butylperoxy)hexane (PA6/HDPE/MAH/L-101) composites were investigated by differential scanning calorimetry (DSC). The crystallization kinetics under non-isothermal condition was analyzed by the Jeziorny and Mo equations, and the activation energy was determined by the Kissinger and Takhor methods. The crystal structure and morphology were analyzed by wide-angle X-ray diffraction (WXRD) and polarized optical microscopy (POM). The results indicate that PA6/HDPE/MAH/L-101 has higher crystallization temperature and crystallization rate, which is explained as due to its heterogeneous nuclei.

scholarly journals The effect of isothermal crystallization on mechanical properties of poly(ethylene 2,5-furandicarboxylate)

e-Polymers ◽  
2021 ◽  
Vol 22 (1) ◽  
pp. 1-11
Author(s):  
Wei Zhang ◽  
Qingyin Wang ◽  
Gongying Wang ◽  
Shaoying Liu
Keyword(s):  
Mechanical Properties ◽  
Intrinsic Viscosity ◽  
Crystallization Temperature ◽  
Isothermal Crystallization ◽  
Tensile Modulus ◽  
Optical Microscope ◽  
Crystallization Time ◽  
Scanning Calorimetry ◽  
Crystallization Properties ◽  
Poly Ethylene

Abstract The effects of isothermal crystallization temperature/time on mechanical properties of bio-based polyester poly(ethylene 2,5-furandicarboxylate) (PEF) were investigated. The intrinsic viscosity, crystallization properties, thermal properties, and microstructure of PEF were characterized using ubbelohde viscometer, X-ray diffraction, polarizing optical microscope, differential scanning calorimetry, and scanning electron microscopy. The PEF sample isothermal crystallized at various temperatures for various times was denoted as PEF-T-t. The results showed that the isothermal crystallization temperature affected the mechanical properties of PEF-T-30 by simultaneously affecting its crystallization properties and intrinsic viscosity. The isothermal crystallization time only affected the crystallization properties of PEF-110-t. The crystallinity of PEF-110-40 was 17.1%. With small crystal size, poor regularity, and α′-crystal, PEF-110-40 can absorb the energy generated in the tensile process to the maximum extent. Therefore, the best mechanical properties can be obtained for PEF-110-40 with the tensile strength of 43.55 MPa, the tensile modulus of 1,296 MPa, and the elongation at a break of 13.36%.

PP/MWCNTs composites: Effects of length of MWCNTs on isothermal crystallization behaviors, crystalline structure, and thermal stability

2017 ◽  
Vol 52 (4) ◽  
pp. 503-517 ◽  
Author(s):  
Zheng-Ian Lin ◽  
Ching-Wen Lou ◽  
Yi-Jun Pan ◽  
Chien-Teng Hsieh ◽  
Chien-Lin Huang ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Thermal Stability ◽  
Crystalline Structure ◽  
Isothermal Crystallization ◽  
Crystallization Rate ◽  
Nucleating Agent ◽  
Scanning Calorimetry ◽  
Crystallization Behaviors ◽  
Walled Carbon Nanotubes ◽  
Thermal Stability Of

This study adopts the melt compounding method to prepare /mutli-walled carbon nanotubes composites. The effects of different lengths of the mutli-walled carbon nanotubes on the isothermal crystallization behaviors, crystalline structure, and thermal stability of the polypropylene/mutli-walled carbon nanotubes composites are examined. The PLM results show that the combination of mutli-walled carbon nanotubes prevents the growth of polypropylene spherulites, and thus results in a small size of spherulites. The differential scanning calorimetry results show that the short (S-) or long (L-) mutli-walled carbon nanotubes can function as the nucleating agent of polypropylene, which accelerates the crystallization rate of polypropylene. Avrami theory analyses indicate that the addition of short-mutli-walled carbon nanotubes particularly provides polypropylene/mutli-walled carbon nanotubes composites with a high crystallization rate. The X-ray diffraction results show that the combination of mutli-walled carbon nanotubes does not pertain to the crystal structure. The TGA test results show that long-mutli-walled carbon nanotubes outperform short -mutli-walled carbon nanotubes in improving the thermal stability of polypropylene, and both can significantly improve it.

The properties of sericin/poly(vinyl alcohol) films modified by boric acid

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Qun Wang ◽  
Lu Qi
Keyword(s):  
Mechanical Properties ◽  
Thermal Stability ◽  
Boric Acid ◽  
Vinyl Alcohol ◽  
Water Resistance ◽  
Poly Vinyl Alcohol ◽  
Scanning Calorimetry ◽  
Blend Ratio ◽  
Percutaneous Drug Delivery ◽  
Thermal Stability Of

AbstractA group of films mainly composed of sericin and poly(vinyl alcohol) (PVA), using boric acid (BA) as a modifier, were prepared by a technique of solution casting. In this work, the effect of BA and sericin on the mechanical properties and water resistance of the films was analyzed, the interior morphology of the films were described by a scanning electron microscopy (SEM), the thermal stability of the films was characterized by differential scanning calorimetry (DSC), and the reaction mechanism was proposed according to the previous literature and the test of Fourier transform infrared spectrum (FTIR). Results indicated that, the properties of the membrane were the functions of the blend ratio of sercin to PVA and the content of BA. The use of BA increased the tensile strength, improved the water resistance and the thermal stability, and varied the interior morphology of the films. The content of sericin greatly influenced the combination of properties of the films, especially the mechanical properties, interior morphology, thermal stability, and water resistance reducing with the increasing of sericin content. The films have potential to be used in materials, such as skin-care coatings for beauty, percutaneous drug delivery systems for exterior intact skin, due to the characteristics of the components and the good mechanical properties of the films.

scholarly journals Combined Effects of Cellulose Nanofiber Nucleation and Maleated Polylactic Acid Compatibilization on the Crystallization Kinetic and Mechanical Properties of Polylactic Acid Nanocomposite

Polymers ◽  
2021 ◽  
Vol 13 (19) ◽  
pp. 3226
Author(s):  
Siti Shazra Shazleen ◽  
Lawrence Yee Foong Ng ◽  
Nor Azowa Ibrahim ◽  
Mohd Ali Hassan ◽  
Hidayah Ariffin
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Polylactic Acid ◽  
Crystallization Kinetics ◽  
Crystallization Kinetic ◽  
Crystallization Rate ◽  
Combined Effects ◽  
Dsc Analysis ◽  
Scanning Calorimetry ◽  
Isothermal Crystallization Kinetics

This work investigated the combined effects of CNF nucleation (3 wt.%) and PLA-g-MA compatibilization at different loadings (1–4 wt.%) on the crystallization kinetics and mechanical properties of polylactic acid (PLA). A crystallization kinetics study was done through isothermal and non-isothermal crystallization kinetics using differential scanning calorimetry (DSC) analysis. It was shown that PLA-g-MA had some effect on nucleation as exhibited by the value of crystallization half time and crystallization rate of the PLA/PLA-g-MA, which were increased by 180% and 172%, respectively, as compared to neat PLA when isothermally melt crystallized at 100 °C. Nevertheless, the presence of PLA-g-MA in PLA/PLA-g-MA/CNF3 nanocomposites did not improve the crystallization rate compared to that of uncompatibilized PLA/CNF3. Tensile strength was reduced with the increased amount of PLA-g-MA. Contrarily, Young’s modulus values showed drastic increment compared to the neat PLA, showing that the addition of the PLA-g-MA contributed to the rigidity of the PLA nanocomposites. Overall, it can be concluded that PLA/CNF nanocomposite has good performance, whereby the addition of PLA-g-MA in PLA/CNF may not be necessary for improving both the crystallization kinetics and tensile strength. The addition of PLA-g-MA may be needed to produce rigid nanocomposites; nevertheless, in this case, the crystallization rate of the material needs to be compromised.

Sign in / Sign up

Export Citation Format

Share Document