The effect of cooling rate on crystallization behavior and tensile properties of CF/PEEK composites

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Guangming Dai ◽  
Lihua Zhan ◽  
Chenglong Guan ◽  
Minghui Huang
Keyword(s):  
Cooling Rate ◽  
Crystallization Temperature ◽  
Crystallization Behavior ◽  
Crystalline Polymer ◽  
Scanning Calorimetry ◽  
Nonisothermal Crystallization ◽  
Cooling Rates ◽  
Control Range ◽  
Temperature Range ◽  
Transverse Tensile

Abstract In this study, the differential scanning calorimetry (DSC) tests were performed to measure the nonisothermal crystallization behavior of carbon fiber reinforced polyether ether ketone (CF/PEEK) composites under different cooling rates. The characteristic parameters of crystallization were obtained, and the nonisothermal crystallization model was established. The crystallization temperature range of the material at different cooling rates was predicted by the model. The unidirectional laminates were fabricated at different cooling rates in the crystallization temperature range. The results showed that the crystallization temperature range shifted to a lower temperature with the increase of cooling rate, the established nonisothermal crystallization model was consistent with the DSC test results. It is feasible to shorten the cooling control range from the whole process to the crystallization range. The crystallinity and transverse tensile strength declined significantly with the increase of the cooling rate in the crystallization temperature range. The research results provided theoretical support for the selection of cooling conditions and temperature control range, which could be applied to the thermoforming process of semi-crystalline polymer matrixed composites to improve the manufacturing efficiency.

Crystallization Behaviour of Polytetrafluoroethylene over very Large Cooling Rate Domains

2013 ◽  
Vol 747 ◽  
pp. 201-204
Author(s):  
Nicolas Bosq ◽  
Nathanaël Guigo ◽  
Nicolas Sbirrazzuoli
Keyword(s):  
Cooling Rate ◽  
Glassy State ◽  
Crystalline Polymer ◽  
Sem Analysis ◽  
Scanning Calorimetry ◽  
Theoretical Dependence ◽  
Cooling Rates ◽  
Fast Scanning Calorimetry ◽  
Wide Range ◽  
Fast Cooling

Polytetrafluoroethylene (PTFE) is a semi-crystalline polymer that demonstrates a very fast crystallization process on cooling. This study investigates the nonisothermal PTFE ultra-fast crystallization over a wide range of cooling rates via conventional Differential Scanning Calorimetry (DSC), Fast Scanning Calorimetry (FSC) and Ultra-Fast Scanning Calorimetry (UFSC). A new knowledge about crystallization kinetics of PTFE is obtained from the data obtained under very fast cooling rates. The shift of the melting peak to lower temperature shows that the crystals formed under fast cooling rates are slightly less stable than those produced under slower cooling rates. SEM analysis allows to observe these differences in crystal morphologies. According to the results, the crystallization is still present even for the fastest cooling rate employed and in consequences it is impossible to reach a metastable glassy state. The effective activation energy (Eα) displays a variation with the relative extent of crystallization (α) that is characteristic of a transition of PTFE crystallization from regime II to regime III around 312°C. Following the Hoffman-Lauritzen theory the Eα dependency obtained from the crystallizations under the different cooling rates was fitted in order to study the theoretical dependence of the growth rate.

Investigation of Nonisothermal Crystallization Behaviors of Poly and Silica Nanocomposites Using Differential Scanning Calorimetry

2005 ◽  
Vol 295-296 ◽  
pp. 39-44 ◽  
Author(s):  
Ling Xue Kong ◽  
Z. Peng
Keyword(s):  
Differential Scanning Calorimetry ◽  
Cooling Rate ◽  
Crystallization Temperature ◽  
Self Assembly ◽  
Degree Of Crystallinity ◽  
Poly Vinyl Alcohol ◽  
Scanning Calorimetry ◽  
Nonisothermal Crystallization ◽  
Crystallization Behaviors ◽  
Silica Nanocomposites

Nonisothermal crystallization behaviors of PVA and poly (vinyl alcohol) and Silica (PVA/SiO2) nanocomposites prepared via a self-assembly monolayer (SAM) technique are investigated in this study. Differential scanning calorimetry (DSC) is used to measure the crystallization temperature and enthalpy of PVA and nanocomposites in nitrogen at various cooling rate. The results show that the degree of crystallinity of PVA and nanocomposites decreases when the SiO2 content increases but increases with an increasing cooling rate. The peak crystallization temperature decreases with an increasing cooling rate.

Properties and Nonisothermal Crystallization Behavior of Nucleated Polylactide Biodegradable Composite Films

2012 ◽  
Vol 488-489 ◽  
pp. 671-675 ◽  
Author(s):  
Worasak Phetwarotai ◽  
Duangdao Aht-Ong
Keyword(s):  
Tensile Properties ◽  
Cooling Rate ◽  
Crystallization Behavior ◽  
Composite Films ◽  
Crystallization Rate ◽  
Nucleating Agent ◽  
Scanning Calorimetry ◽  
Nonisothermal Crystallization ◽  
Precipitated Calcium Carbonate ◽  
Biodegradable Composite

Polylactide biodegradable composite films were prepared via melt extrusion using a twin screw extruder. The effects of type and content of nucleating agent and cooling rate on the thermal and tensile properties of these films were investigated. Two types of nucleating agent, talc and nano precipitated calcium carbonate (NPCC), were studied at various contents from 0 to 2.0 phr. Nonisothermal crystallization behavior of composites was characterized by a differential scanning calorimetry (DSC). The cooling rate was varied from 1 to 10°C/min. The results indicated that the presence of nucleating agent significantly influenced on thermal and tensile properties of the PLA composite films. DSC thermograms revealed that the addition of nucleating agent on the PLA films led to an increase of crystallization temperature (Tc), crystallization rate, and degree of crystallization (χc) compared to the neat PLA. These behaviors could be noticed in both the nucleated PLA films with NPCC and talc. In contrast, the Tc and crystallization half-time (t1/2) of these films significantly decreased when the cooling rate increased from 1 to 10°C/min. However, thermal stability of the films decreased when the nucleating agent content increased, especially that of the composites with NPCC.

Non-isothermal crystallization behavior of spinel crystals in FeO-SiO2-TiO2-V2O3-Cr2O3 slag

2018 ◽  
Vol 116 (1) ◽  
pp. 110
Author(s):  
Lixiong Shao ◽  
Jiang Diao ◽  
Wang Zhou ◽  
Tao Zhang ◽  
Bing Xie
Keyword(s):  
Cooling Rate ◽  
Crystallization Behavior ◽  
Crystal Size ◽  
Growth Mechanisms ◽  
Vanadium Slag ◽  
Growth Behaviour ◽  
Temperature Range ◽  
Chromium Spinel ◽  
Mean Diameter ◽  
The Mean

The growth behaviour of spinel crystals in vanadium slag with high Cr2O3 content was investigated and clarified by statistical analyses based on the Crystal Size Distribution (CSD) theory. The results indicate that low cooling rate and Cr2O3 content benefit the growth of spinel crystals. The chromium spinel crystals firstly precipitated and then acted as the heterogeneous nuclei of vanadium and titanium spinel crystals. The growth mechanisms of the spinel crystals at the cooling rate of 5 K/min consist two regimes: firstly, nucleation control in the temperature range of 1873 to 1773 K, in which the shapes of CSD curves are asymptotic; secondly, surface and supply control within the temperature range of 1773 to 1473 K, in which the shapes of CSD curves are lognormal. The mean diameter of spinel crystals increases from 3.97 to 52.21 µm with the decrease of temperature from 1873 to 1473 K.

scholarly journals Development of Precipitation Hardening Parameters for High Strength Alloy AA 7068

Materials ◽  
2020 ◽  
Vol 13 (4) ◽  
pp. 918
Author(s):  
Julia Osten ◽  
Benjamin Milkereit ◽  
Michael Reich ◽  
Bin Yang ◽  
Armin Springer ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Cooling Rate ◽  
Maximum Yield ◽  
High Strength ◽  
Tensile Tests ◽  
Age Hardening ◽  
Scanning Calorimetry ◽  
Cooling Rates ◽  
Critical Cooling Rate ◽  
Kinetics Of

The mechanical properties after age hardening heat treatment and the kinetics of related phase transformations of high strength AlZnMgCu alloy AA 7068 were investigated. The experimental work includes differential scanning calorimetry (DSC), differential fast scanning calorimetry (DFSC), sophisticated differential dilatometry (DIL), scanning electron microscopy (SEM), as well as hardness and tensile tests. For the kinetic analysis of quench induced precipitation by dilatometry new metrological methods and evaluation procedures were established. Using DSC, dissolution behaviour during heating to solution annealing temperature was investigated. These experiments allowed for identification of the appropriate temperature and duration for the solution heat treatment. Continuous cooling experiments in DSC, DFSC, and DIL determined the kinetics of quench induced precipitation. DSC and DIL revealed several overlapping precipitation reactions. The critical cooling rate for a complete supersaturation of the solid solution has been identified to be 600 to 800 K/s. At slightly subcritical cooling rates quench induced precipitation results in a direct hardening effect resulting in a technological critical cooling rate of about 100 K/s, i.e., the hardness after ageing reaches a saturation level for cooling rates faster than 100 K/s. Maximum yield strength of above 600 MPa and tensile strength of up to 650 MPa were attained.

Role of interfacial interaction on the crystallization behavior and melting characteristics of PP/Nano-CaCO3 composites modified with different compatibilizers

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Yuhai Wang ◽  
Hao Shen ◽  
Gu Li ◽  
Kancheng Mai
Keyword(s):  
Synergistic Effect ◽  
Heterogeneous Nucleation ◽  
Crystallization Temperature ◽  
Crystallization Behavior ◽  
Crystallization Rate ◽  
Interfacial Interaction ◽  
Scanning Calorimetry ◽  
Polar Groups ◽  
Melting Characteristics

AbstractPP/nano-CaCO3 composites with different interfacial interaction were prepared by addition of compatibilizers with the same polar groups but different backbones. The non-isothermal and isothermal crystallization behavior of PP/nano- CaCO3 composites was investigated using differential scanning calorimetry (DSC). The results indicated that the interfacial interaction between PP and nano-CaCO3 increased the crystallization temperature and crystallization rate of PP due to the heterogeneous nucleation of nano-CaCO3. The interfacial interaction between nano- CaCO3 and compatibilizer further increased the crystallization temperature and crystallization rate of PP and induced the formation of β-crystal of PP due to the synergistic effect of heterogeneous nucleation between nano-CaCO3 and compatibilizer. This synergistic effect of heterogeneous nucleation between nano- CaCO3 and compatibilizer depended on the interfacial interaction between compatibilizer and PP matrix. The increased compatibility between compatibilizer and PP matrix favoured the heterogeneous nucleation between nano-CaCO3 and compatibilizer

Nonisothermal Crystallization Behavior of Poly(vinylidenefluoride)/Polysulfone/Diethylene Glycol Dibenzoate/Dibutyl Phthalate System via Thermally Induced Phase Separation

2015 ◽  
Vol 1120-1121 ◽  
pp. 581-585
Author(s):  
Jing Zhang ◽  
Lu Qi ◽  
Zhen Yu Cui
Keyword(s):  
Phase Separation ◽  
Diethylene Glycol ◽  
Crystallization Behavior ◽  
Dibutyl Phthalate ◽  
Vinylidene Fluoride ◽  
Thermally Induced Phase Separation ◽  
Scanning Calorimetry ◽  
Nonisothermal Crystallization ◽  
Thermally Induced ◽  
Poly Vinylidene Fluoride

Differential scanning calorimetry (DSC) measurement is used to investigate the nonisothermal crystallization behavior of poly (vinylidene fluoride) (PVDF)/polysulfone (PSF)/diethylene glycol dibenzoate (DEDB)/dibutyl phthalate (DBP) system via solid-liquid (S-L) phase separation during a thermally induced phase separation process. The effect of benzene ring in PSF on PVDF crystallization for PVDF/PSF/DEDB/DBP system is investigated. It is found that the Ozawa model can describe nonisothermal crystallization behavior of PVDF/PSF/DEDB/DBP system in a certain crystallization temperature range. Jeziorny method indicates that the secondary crystallization of PVDF exists in the process of nonisothermal crystallization and is enhanced by the increase of cooling rate.

scholarly journals Non-Isothermal Crystallization Kinetics of Poly(4-Hydroxybutyrate) Biopolymer

Molecules ◽  
2019 ◽  
Vol 24 (15) ◽  
pp. 2840 ◽  
Author(s):  
Ina Keridou ◽  
Luis J. del Valle ◽  
Lutz Funk ◽  
Pau Turon ◽  
Lourdes Franco ◽  
...  
Keyword(s):  
Growth Rate ◽  
Cooling Rate ◽  
Crystallization Temperature ◽  
Isothermal Crystallization ◽  
Secondary Nucleation ◽  
Scanning Calorimetry ◽  
Limited Region ◽  
First Case ◽  
Biodegradable Poly ◽  
Insertion Mechanism

The non-isothermal crystallization of the biodegradable poly(4-hydroxybutyrate) (P4HB) has been studied by means of differential scanning calorimetry (DSC) and polarizing optical microscopy (POM). In the first case, Avrami, Ozawa, Mo, Cazé, and Friedman methodologies were applied. The isoconversional approach developed by Vyazovkin allowed also the determination of a secondary nucleation parameter of 2.10 × 105 K2 and estimating a temperature close to 10 °C for the maximum crystal growth rate. Similar values (i.e., 2.22 × 105 K2 and 9 °C) were evaluated from non-isothermal Avrami parameters. All experimental data corresponded to a limited region where the polymer crystallized according to a single regime. Negative and ringed spherulites were always obtained from the non-isothermal crystallization of P4HB from the melt. The texture of spherulites was dependent on the crystallization temperature, and specifically, the interring spacing decreased with the decrease of the crystallization temperature (Tc). Synchrotron data indicated that the thickness of the constitutive lamellae varied with the cooling rate, being deduced as a lamellar insertion mechanism that became more relevant when the cooling rate increased. POM non-isothermal measurements were also consistent with a single crystallization regime and provided direct measurements of the crystallization growth rate (G). Analysis of the POM data gave a secondary nucleation constant and a bell-shaped G-Tc dependence that was in relative agreement with DSC analysis. All non-isothermal data were finally compared with information derived from previous isothermal analyses.

Detection of Quench Induced Precipitation in Al Alloys by Dilatometry

2016 ◽  
Vol 877 ◽  
pp. 147-152 ◽  
Author(s):  
Benjamin Milkereit ◽  
Michael Reich ◽  
Olaf Kessler
Keyword(s):  
Cooling Rate ◽  
High Strength ◽  
Al Alloys ◽  
Age Hardening ◽  
Controlled Cooling ◽  
Scanning Calorimetry ◽  
Cooling Rates ◽  
Precipitation Behaviour ◽  
In Situ Detection

Quenching is a critical step during the strengthening age hardening of Aluminium alloys. To obtain optimal technological results, parts should be quenched with the upper critical cooling rate. The precipitation behaviour of Al alloys during cooling from solution annealing and thereby the critical cooling rates are typically investigated by in-situ measurements with differential scanning calorimetry (DSC). Conventional DSCs are limited at cooling rates below 10 Ks-1. Unfortunately, medium to high strength Al alloys typically have critical cooling rates between 10 and some 100 Ks-1. Recently it was shown that dilatometry is generally able for in-situ detection of precipitation in Al alloys. Dilatometry allows controlled cooling up to some 100 Ks-1 and therefore covers the cooling rate range relevant. In this work, we aim to show up and discuss possibilities and limitations of dilatometric detection of quench induced precipitates in 2xxx, and 7xxx Al alloys. The basic method will be presented and results will be compared with DSC work.

Influence of Cooling Rates on Phase Transitions of Bent-Core Liquid Crystal 1,3-Phenylene-bis[4-(hexylcarboyloxyl)benzylideneamine]

2010 ◽  
Vol 428-429 ◽  
pp. 247-250 ◽  
Author(s):  
Yuan Ming Huang ◽  
Qing Lan Ma ◽  
Bao Gai Zhai
Keyword(s):  
Differential Scanning Calorimetry ◽  
Phase Transitions ◽  
Liquid Crystal ◽  
Optical Microscopy ◽  
Cooling Rate ◽  
Scanning Calorimetry ◽  
Slow Cooling ◽  
Cooling Rates ◽  
Polarized Optical Microscopy ◽  
Fast Cooling

The influence of cooling rate on the phase transitions of a three-benzene-ring containing bent-core liquid crystal 1,3-phenylene-bis[4-(hexylcarboyloxyl)benzylideneamine] has been investigated by means of differential scanning calorimetry and polarized optical microscopy. Our results show that the cooling rates in the second cooling run pose significant effects on the phase transitions of the bent-core liquid crystal despite the cooling rates in the first cooling run pose little effects on the phase transitions. In the second cooling run, the banana phases survived only when the cooling rates were in the range of 14~15oC/min whereas both slow cooling rates which were less than 13oC/min and fast cooling rates which were higher than 16oC/min made the banana phases disappeared.

Sign in / Sign up

Export Citation Format

Share Document