scholarly journals Synthesis and Physical Properties of Non-Crystalline Nylon 6 Containing Dimer Acid

Polymers ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 386 ◽  
Author(s):  
Ching-Nan Huang ◽  
Chang-Mou Wu ◽  
Hao-Wen Lo ◽  
Chiu-Chun Lai ◽  
Wei-Feng Teng ◽  
...  

In this study, a long carbon chain dimer acid is introduced into a nylon 6 structure and is copolymerized with different structural amines to produce amorphous nylon 6 by 4,4′-methylenebis(2-methylcyclohexylamine) (MMCA) in different copolymerization ratios. The effect of different structures and copolymerization ratios on the properties of nylon 6 is determined, along with the thermal properties, crystallinity, water absorption, dynamic mechanical properties, and optical properties. It is found that the melting point and the thermal cracking temperature Td10 of nylon 6 are respectively between 176 °C and 213 °C and 378 °C to 405 °C. The effect of introducing a bicyclohexane group containing a methyl side chain is greater than that of a meta-benzene ring, so COMM (synthesized by Caprolactam (C), dimer oleic acid (OA), and 4,4′-Methylenebis(2-methylcyclohexylamine) (MMCA)) has the lowest melting point, enthalpy, and crystallinity. As the copolymerization ratio increases, its thermal properties decrease. 10% is the lowest crystallinity. The amine structure containing a bicycloalkyl group has lower water absorption and a 10% copolymerization ratio gives the lowest water absorption. It contains the bicycloalkyl group, COM (synthesized by Caprolactam (C), dimer oleic acid (OA) and 4,4′-Methylenebis(cyclohexylamine) (MCA)), which has the highest loss modulus. The lowest loss modulus is noted for a copolymerization ratio of 7% and the value of tan δ increases as the copolymerization ratio increases. The introduction of nylon 6 with the bicycloalkyl groups, COMM and COM, significantly increases transparency. As the copolymerization ratio increases, the transparency increases and the haze decreases. The best optical properties are achieved for 10% copolymerization.

2020 ◽  
Vol 34 (07n09) ◽  
pp. 2040005
Author(s):  
Chiu-Chun Lai ◽  
Bo-Sien Yu ◽  
Hao-Wen Lo ◽  
Wei-Feng Teng ◽  
Lung-Chang Liu ◽  
...  

In this research, a series of amorphous nylons 6 were prepared by introducing adipic acid and different structure amines into the copolymerization with caprolactam. The effects including thermal properties, crystallinity, dynamic mechanical properties, optical properties, and water absorption of different copolymerization structure and copolymerization ratio on the properties of nylon 6 were investigated. The results show the melting point and thermal cracking temperature Td 5 of nylon 6 are, respectively, between 179[Formula: see text]C and 217[Formula: see text]C and 278[Formula: see text]C to 336[Formula: see text]C. Nylon 6 structure introducing a methyl side chain is more effective than a meta-benzene ring, a meta-cycloalkyl, and bicycloalkyl groups, so CAMM and CAI have the lowest crystallinity.


Polymers ◽  
2021 ◽  
Vol 13 (14) ◽  
pp. 2349
Author(s):  
Alain Salvador Conejo-Dávila ◽  
Marco Armando Moya-Quevedo ◽  
David Chávez-Flores ◽  
Alejandro Vega-Rios ◽  
Erasto Armando Zaragoza-Contreras

The development of anilinium 2-acrylamide-2-methyl-1-propanesulfonate (Ani-AMPS) monomer, confirmed by 1H NMR, 13C NMR, and FTIR, is systematically studied. Ani-AMPS contains two polymerizable functional groups, so it was submitted to selective polymerization either by free-radical or oxidative polymerization. Therefore, poly(anilinium 2-acrylamide-2-methyl-1-propanesulfonic) [Poly(Ani-AMPS)] and polyaniline doped with 2-acrylamide-2-methyl-1-propanesulfonic acid [PAni-AMPS] can be obtained. First, the acrylamide polymer, poly(Ani-AMPS), favored the π-stacking of the anilinium group produced by the inter- and intra-molecular interactions and was studied utilizing 1H NMR, 13C NMR, FTIR, and UV-Vis-NIR. Furthermore, poly(Ani-AMPS) fluorescence shows quenching in the presence of Fe2+ and Fe3+ in the emission spectrum at 347 nm. In contrast, the typical behavior of polyaniline is observed in the cyclic voltammetry analysis for PAni-AMPS. The optical properties also show a significant change at pH 4.4. The PAni-AMPS structure was corroborated through FTIR, while the thermal properties and morphology were analyzed utilizing TGA, DSC (except PAni-AMPS), and FESEM.


Proceedings ◽  
2020 ◽  
Vol 69 (1) ◽  
pp. 38
Author(s):  
Celia Idres ◽  
Mustapha Kaci ◽  
Nadjet Dehouche ◽  
Idris Zembouai ◽  
Stéphane Bruzaud

This paper aims to investigate the effect of different chemical modifications of biocomposites based on poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBH) and aloe vera bio-fibers incorporated at 20 wt%. The fiber surface was modified with alkaline, organosilanes, and combined alkaline/organosilanes. Surface morphology, thermal stability, water absorption capacity, and rheological behavior of the modified biocomposite materials were studied, and the results compared to both unmodified biocomposites and neat PHBH. The study showed that the modified biocomposites with both alkaline and organosilanes exhibited an improved surface morphology, resulting in a good fiber/matrix interfacial adhesion. As a result, increases in complex viscosity, storage modulus, and loss modulus were observed, whereas water absorption was reduced. Thermal stability remained almost unchanged, with the exception of the biocomposite treated with alkaline, where this property decreased significantly. Finally, the coupling of alkaline and organosilane modification is an efficient route to enhance the properties of PHBH biocomposites.


2018 ◽  
Vol 775 ◽  
pp. 26-31
Author(s):  
Sukantika Manatsittipan ◽  
Kamonthip Kuttiyawong ◽  
Kazuo Ito ◽  
Sunan Tiptipakorn

In this study, the biodegradability and thermal properties the composites of polybutylene succinate (PBS) and chitosan of different molecular weights (Mn = 104,105, and 106 Da) were prepared at chitosan contents of 0-10 wt%. After 10 days of microbial degradation, the results show that the amount of holes from degradation was increased with either decreasing Mn or increasing chitosan contents. However, the size of holes was increased with increasing Mn and chitosan contents. The results from Differential Scanning Calorimeter (DSC) present that the melting temperature (Tm) of PBS was decreased with increasing chitosan contents. Moreover, there was no significant difference between Tm of the composites with different Mn of chitosan. From the TGA thermograms, the decomposition temperature at 10% weight loss (Td10) was decreased with increasing chitosan contents. Moreover, the water absorption of PBS/chitosan composites was increased with increasing Mn and content of chitosan.


2014 ◽  
Vol 1052 ◽  
pp. 242-248
Author(s):  
Hong Kai Zhao ◽  
Hong Li Wang

Through the polymerization and grafting reaction of bisphenol A dianhydride and bisphenol A diamine, the polyimide activator (PI activator) of acyl caprolactam end capping is obtained and then the anionic in-situ polymerization modified nylon 6 resin is obtained. Viscosity analysis shows that PI consumption is higher than 0.1 (of monomer mass), the reaction temperature is higher than 160°C, the viscosity rises rapidly in a short time and the rapid polymerization molding can be realized; when PI consumption is higher than 0.15 (of monomer mass), the water absorption of matrix resin will be lower than 1.4%; compared with the nylon resin, its water absorption is significantly lowered and its mechanical property is improved greatly; microscopic analysis shows that PI molecules fail to enter the crystalline phase of the nylon 6 and form lamellar crystals in the nylon matrix, which plays a role of enhancement and obstruction; differential thermal analysis shows that PI reduces the melting enthalpy and melting point temperature of nylon 6 resin, which indicates that PI reduces the crystallization capacity of nylon 6.


1998 ◽  
Vol 519 ◽  
Author(s):  
C. Kumudinie ◽  
J. K. Premachandra ◽  
J. E. Mark ◽  
T. D. Dang ◽  
M. R. Unroe ◽  
...  

AbstractHigh-temperature poly(arylene ether) and hydroxypolybenzoxazole polymers were toughened using dispersed rubbery phases. This rubbery phase was a hybrid material which was in-situ generated within the polymer matrix using mixtures of partially-hydrolyzable trialkoxy and dialkoxy organosilanes with a fully hydrolyzable tetraalkoxysilane. The resulting materials were characterized with regard to their structures, mechanical properties (modulus, ultimate strength, maximum extensibility, and toughness), thermal properties, optical properties, and tendencies to absorb water. Some of the results are presented here.


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