scholarly journals Effect of Bis (2-Aminoethyl) Adipamide/Adipic Acid Segment on Polyamide 6: Crystallization Kinetics Study

Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1067 ◽  
Author(s):  
Yu-Hao Chen ◽  
Palraj Ranganathan ◽  
Chin-Wen Chen ◽  
Yi-Huan Lee ◽  
Syang-Peng Rwei
Keyword(s):  
Crystallization Kinetics ◽  
Adipic Acid ◽  
Crystallization Behavior ◽  
Three Dimensional ◽  
Isothermal Condition ◽  
Crystallization Rate ◽  
Polyamide 6 ◽  
X Ray Diffraction ◽  
Dimensional Growth ◽  
Complex Polymer

The crystallization behavior of novel polyamide 6 (PA6) copolyamides with different amounts of bis (2-aminoethyl) adipamide/adipic acid (BAEA/AA) segment was investigated. The wide-angle X-ray diffraction (WAXD) results showed that as the amount of BAEA/AA segment increased to 10 mole%, the crystalline forms of all PA6 copolyamide were transferred from the stable α-form to the unstable γ-form because of the complex polymer structure. According to studies of crystallization kinetics, the Avrami exponent (n) values for all copolyamide samples ranged from 1.43 to 3.67 under isothermal conditions, implying that the crystallization is involved in the two- to three-dimensional growth at a high temperature of isothermal condition. The copolyamides provided a slower crystallization rate and higher crystallization activation energy (ΔEa) than neat PA6. Polyamide containing 10 mole% of BEAE/AA content exhibited a unique crystallization behavior in the coexistence of the α and γ forms. These results deepen our understanding of the relationship between BAEA/AA content, crystal structure, and its crystallization behavior in low-melting PA6, and they make these types of copolyamides useful for their practical application.

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 Isothermal Crystallization Kinetics Study of Fully Aliphatic PA6 Copolyamides: Effect of Novel Long-Chain Polyamide Salt as a Comonomer

Polymers ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 472 ◽  
Author(s):  
Syang-Peng Rwei ◽  
Palraj Ranganathan ◽  
Yi-Huan Lee
Keyword(s):  
Crystallization Kinetics ◽  
Isothermal Crystallization ◽  
Three Dimensional ◽  
Sebacic Acid ◽  
Crystallization Rate ◽  
Polyamide 6 ◽  
Crystallization Time ◽  
Structure Property ◽  
Isothermal Crystallization Kinetics ◽  
Half Crystallization Time

N1, N6-bis (4-aminobutyl) adipamide (BABA) diamine and sebacic acid (SA), also called BABA/SA polyamide salt, were used in a typical melt polymerization processes of polyamide 6 (PA6) to form a series of PA6-BABA/SA copolyamides. The effects of BABA/SA on the isothermal crystallization kinetics of PA6-BABA/SA were studied for the first time. An isothermal crystallization analysis demonstrates that the PA6-BABA/SA matrix provided a higher crystallization rate and shorter half-crystallization time than virgin PA6 did. The degree of crystallization of the PA6-BABA/SA30 matrix was also the lowest among all of the samples considered herein. This result is attributed to the high nucleation efficacy of a small amount of BABA/SA in the crystallization of PA6. Values of the Avrami exponent (n) from 1.84 to 3.91 were observed for all of the polyamide samples, suggesting that the crystallization was involved via a two- to three-dimensional growth mechanism. These findings deepen our understanding of the structure–property relationship of PA6-BABA/SA copolyamides, favoring their practical application.

Non-Isothermal Crystallization Kinetics of Graphene Oxide-Carbon Nanotubes Hybrids / Polyamide 6 Composites

2019 ◽  
Vol 41 (3) ◽  
pp. 394-394
Author(s):  
Zhi Qiang Wang Zhi Qiang Wang ◽  
Yong Ke Zhao and Xiang Feng Wu Yong Ke Zhao and Xiang Feng Wu
Keyword(s):  
Carbon Nanotubes ◽  
Graphene Oxide ◽  
Cooling Rate ◽  
Crystallization Kinetics ◽  
Isothermal Crystallization ◽  
Crystallization Rate ◽  
Polyamide 6 ◽  
Degree Of Crystallinity ◽  
Isothermal Crystallization Kinetics ◽  
Kinetics Of

The hybrids combined by nano-materials with different dimensions usually possess much better enhancement effects than single one. Graphene oxide-carbon nanotubes hybrids / polyamide 6 composites has been fabricated. The non-isothermal crystallization kinetics of the as-prepared samples was discussed. Research results showed that increasing the cooling rate was in favor of increasing the crystallization rate and the degree of crystallinity for the as-prepared samples. Moreover, the crystallization rate was first decreased and then increased with increasing the hybrids loading. Furthermore, the crystallization mechanism was changed with increasing the crystallization temperature and the cooling rate. The nucleation and growth modes of the non-isothermal crystallization could be classified into three different types, according to the Ozawa’s theory. These complicated results could be attributed to the important role of crystallization rate as well as the simultaneous hindering and promoting effects of the as-prepared hybrids. This work has reference values for understanding the crystallization kinetics of the polyamide 6-based composites.

The Effect of Acidity Coefficient on Crystallization Behavior of Blast Furnace Slag Fibers

2018 ◽  
Vol 37 (1) ◽  
pp. 33-37
Author(s):  
Tie-Lei Tian ◽  
Yu-Zhu Zhang ◽  
Hong-wei Xing ◽  
Jie Li ◽  
Zun-Qian Zhang
Keyword(s):  
Thermal Stability ◽  
Crystallization Kinetics ◽  
Blast Furnace Slag ◽  
Chemical Structure ◽  
Crystallization Behavior ◽  
Three Dimensional ◽  
Mineral Wool ◽  
Mineral Wool Fiber ◽  
Kinetics Of ◽  
Furnace Slag

AbstractThe chemical structure of mineral wool fiber was investigated by using Fourier Transform Infrared Spectroscopy (FTIR). Next, the glass transition temperature and the crystallization temperature of the fibers were studied. Finally, the crystallization kinetics of fiber was studied. The results show that the chemical bond structure of fibers gets more random with the increase of acidity coefficient. The crystallization phases of the fibers are mainly melilites, and also a few anorthites and diopsides. The growth mechanism of the crystals is three dimensional. The fibers with acidity coefficient of 1.2 exhibit the best thermal stability and is hard to crystallize as it has the maximum aviation energy of crystallization kinetics.

scholarly journals Effect of B2O3 on the Crystallization Behavior of CaF2-Based Slag for Electroslag Remelting 9CrMoCoB Steel

Metals ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1331
Author(s):  
Leizhen Peng ◽  
Zhouhua Jiang ◽  
Xin Geng ◽  
Fubin Liu ◽  
Huabing Li
Keyword(s):  
Activation Energy ◽  
Crystallization Behavior ◽  
Three Dimensional ◽  
Electroslag Remelting ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Caf2 Crystal ◽  
B2o3 Content ◽  
Good Surface ◽  
Ingot Quality

The non-isothermal crystallization characteristics of the electroslag remelting (ESR)-type slag with varied B2O3 contents were investigated by non-isothermal differential scanning calorimetry (DSC), field emission scanning electron microscopy (SEM-EDS), and X-ray diffraction (XRD). The crystallization mechanism of the B2O3-bearing slag was also identified based on kinetics analysis. The results showed that the primary crystalline phase was CaF2, there was no change in the type of the primary crystal as B2O3 content increased, and the morphology of the CaF2 crystal was mainly dendritic. The sequence of crystal precipitation during the cooling process was CaF2 to Ca12Al14O32F2 and MgO/MgAl2O4, followed by Ca3B2O6. The activation energy of CaF2 crystallization increased firstly, then decreased and reached stability, while the activation energy of Ca3B2O6 crystallization increased continuously with the increasing B2O3 content. The crystallization behavior of CaF2 was three-dimensional growth with a constant nucleation rate. The proper B2O3 content added into the CaF2-based ESR slag should be around 1.0% to limit the precipitation of the CaF2 crystal to attain good surface ingot quality and stable ESR operation.

scholarly journals Kinetic studies on leucite precursors

2009 ◽  
Vol 7 (2) ◽  
pp. 205-210 ◽  
Author(s):  
Martina Mrázová ◽  
Alexandra Kloužková ◽  
Martina Kohoutková
Keyword(s):  
Kinetic Equations ◽  
Three Dimensional ◽  
Kinetic Studies ◽  
X Ray Diffraction ◽  
X Ray ◽  
Average Value ◽  
Activation Energy Of Crystallization ◽  
Calculated Activation Energy ◽  
Dimensional Growth ◽  
Calculated Activation

AbstractKinetic studies were performed on two types of leucite precursors. These precursors were prepared using a hydrothermal method at 150°C; the reaction time was 1.5 hours. In order to obtain precursors having different amounts of seed the molarity of KOH was changed. These intermediate products were subsequently calcinated from 5 minutes to 72 hours at temperatures of 850°C, 900°C, 950°C, 1000°C and 1050°C. The crystallinities of the powders were calculated by X-ray diffraction analysis. The crystallization curves for the synthesis of leucite exhibited a typical sigmoidal characteristic. Using different kinetic equations it was found that the Avrami-Eroféev model is the most appropriate to describe the experimental data. Using the Avrami-Eroféev model n reaches an average value of 2.9 which is connected with the three-dimensional growth of nuclei. The calculated activation energy of crystallization of leucite was 385 kJ mol-1 for non-seeded precursors and 246 kJ mol-1 for seeded precursors, respectively.

Effects of Attapulgite on the Isothermal Crystallization Behavior of Poly(Butylene Succinate-co-Butylene Adipate)

2013 ◽  
Vol 791-793 ◽  
pp. 56-59
Author(s):  
Zhi Guo Qi ◽  
Jin Nan Chen ◽  
Bao Hua Guo ◽  
Yu Zhang
Keyword(s):  
Crystallization Kinetics ◽  
Crystallization Temperature ◽  
Isothermal Crystallization ◽  
Crystallization Behavior ◽  
Growth Form ◽  
Crystallization Rate ◽  
Melt Mixing ◽  
Butylene Succinate ◽  
Isothermal Crystallization Kinetics ◽  
Kinetics Of

Poly (butylene succinate-co-butylene adipate)/attapulgite nanocomposites were prepared by melt mixing in a HAAKE mixer. The crystallization kinetics of PBSA and its nanocomposites was studied under isothermal conditions by differential scanning calorimetr. The isothermal crystallization kinetics results indicated that attapulgite can induce heterogeneous nucleation, resulting in an improvement on the crystallization temperature and crystallization rate. Both the PBSA and its nanocomposites were correlated to the spherulitic growth form.

Crystallization Behavior of PLA/PEG/Nucleating Agent Blends

2013 ◽  
Vol 807-809 ◽  
pp. 578-581 ◽  
Author(s):  
Jin Xu Dai ◽  
Qiang Yang ◽  
Bao Jian Liu
Keyword(s):  
Crystal Structure ◽  
Polyethylene Glycol ◽  
Crystallization Behavior ◽  
Crystallization Rate ◽  
Nucleating Agent ◽  
Nucleating Agents ◽  
X Ray Diffraction ◽  
X Ray ◽  
Crystallization Ability ◽  
Co Precipitation

A series of PLA blends were prepared by solution co-precipitation of polylactide (PLA), polyethylene glycol (PEG) and different crystallization nucleating agents. The crystallization behavior of blends was investigated by differential scanning calorimeter (DSC) and X-ray diffraction (XRD). The results showed that the crystallization ability of PLA blends was accelerated by plasticizer PEG, but the crystal structure of the obtained PLA blends was imperfect; the crystal structure and crystallization rate of the PLA blends were improved with the addition of nucleating agent, moreover, the crystallinity was 34.1% and 36.5%, respectively.

scholarly journals Effect of 1,2,4,5-Benzenetetracarboxylic Acid on Unsaturated Poly(butylene adipate-co-butylene itaconate) Copolyesters: Synthesis, Non-Isothermal Crystallization Kinetics, Thermal and Mechanical Properties

Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1160 ◽  
Author(s):  
Chin-Wen Chen ◽  
Te-Sheng Hsu ◽  
Kuan-Wei Huang ◽  
Syang-Peng Rwei
Keyword(s):  
Mechanical Properties ◽  
Crystallization Kinetics ◽  
Isothermal Crystallization ◽  
Crystallization Behavior ◽  
Crystallization Rate ◽  
Cross Linking ◽  
Thermal And Mechanical Properties ◽  
Isothermal Crystallization Kinetics ◽  
Melt Polymerization ◽  
Thermal Mechanical Properties

Unsaturated poly (butylene adipate-co-butylene itaconate) (PBABI) copolyesters were synthesized through melt polymerization composed of 1,4-butanediol (BDO), adipic acid (AA), itaconic acid (IA) and 1,2,4,5-benzenetetracarboxylic acid (BTCA) as a cross-linking modifier. The melting point, crystallization and glass transition temperature of the PBABI copolyesters were detected around 29.8–49 °C, 7.2–29 °C and −51.1 and −58.1 °C, respectively. Young’s modulus can be modified via partial cross-linking by BTCA in the presence of IA, ranging between 32.19–168.45 MPa. Non-isothermal crystallization kinetics were carried out to explore the crystallization behavior, revealing the highest crystallization rate was placed in the BA/BI = 90/10 at a given molecular weight. Furthermore, the thermal, mechanical properties, and crystallization rate of PBABI copolyesters can be tuned through the adjustment of BTCA and IA concentrations.

scholarly journals Analysis of the rheological property and crystallization behavior of polylactic acid (Ingeo™ Biopolymer 4032D) at different process temperatures

e-Polymers ◽  
2021 ◽  
Vol 21 (1) ◽  
pp. 702-709
Author(s):  
Hyeong Min Yoo ◽  
Su-Yeon Jeong ◽  
Sung-Woong Choi
Keyword(s):  
Rheological Property ◽  
Polylactic Acid ◽  
Crystallization Kinetics ◽  
Crystallization Behavior ◽  
Crystallization Rate ◽  
Avrami Equation ◽  
Scanning Calorimetry ◽  
Isothermal Crystallization Kinetics ◽  
Shear Rates ◽  
Kinetics Of

Abstract The aim of this study was to determine the rheological property and crystallization behavior of polylactic acid (PLA) with improved heat resistance (Ingeo™ Biopolymer 4032D) through investigation of the melt viscosity and crystallization kinetics of PLA at different process temperatures. The viscosity was measured using a rotational rheometer under conditions of shear rates of 0.01, 0.1, and 1/s. The obtained rheological data show that the viscosity tended to decrease slightly as the shear rate increases and decrease sharply as the temperature increases from 180°C to 210°C. To investigate the effect of the process temperature on the crystallization kinetics and final crystallinity of PLA, thermal analysis using isothermal differential scanning calorimetry (DSC) were also performed. The Avrami equation was successfully applied for the isothermal crystallization kinetics model. From crystallization temperature of 85°C to 120°C, we found that the Ingeo™ Biopolymer 4032D PLA had the fastest crystallization rate (t 1/2: 26.0 min) and the largest crystallinity (47.4%) at 100°C.

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