Influence of moisture/water absorption on mechanical and thermal properties of polyamide6/boric oxide composites

2021 ◽  
Vol ahead-of-print (ahead-of-print) ◽  
Author(s):  
Kawaljit Singh Randhawa ◽  
Ashwin Patel

Purpose This paper aims to investigate the mechanical and thermal behavior, i.e. tensile strength, hardness, impact strength and glass transition temperatures of water-treated polyamide6/boric oxide (PA) composites. Design/methodology/approach The PA6 and PA6/boric oxide composites were exposed to an open environment and immersed in water for 15 days to analyze the effect of environmental humidity and frequent water immersion conditions on the composite’s mechanical and thermal properties. The tensile strength, elastic modulus, hardness and impact strength of materials were measured to identify the mechanical properties. The scanning electron microscopy (SEM), X-ray diffraction (XRD) and differential scanning calorimetry (DSC) characterizations were used to see the effect of humidity/water absorption on microstructure, crystallinity and glass transition temperatures. Findings The testing results revealed the loss in strength, elastic modulus and hardness, while the impact resistance was improved after exposure of materials to humidity/water. SEM images clearly show the formation of voids and XRD graphs revealed the loss in crystallinity after water immersion. The DSC plots of water immersed materials revealed the loss of glass transition temperatures up to 15°C. Originality/value The mechanical and thermal behavior of PA composites varies according to the surrounding atmosphere. Experiments were performed to investigate the influence of water treatment on the PA6/B2O3 composite’s mechanical and thermal properties. Water treatment resulted in the bonding between PA and water molecules, which generated voids in the materials. These voids generations are found the main reason for the low strength and hardness of water-treated materials.

2021 ◽  
Vol ahead-of-print (ahead-of-print) ◽  
Author(s):  
Kawaljit Singh Randhawa ◽  
Ashwin Patel

PurposeThe absorption of moisture/water can affect the mechanical and thermal properties of polymers and polymer composites as many polymers, mainly polyamide thermoplastics, are sensitive to environmental humidity and can absorb a large amount of moisture. This paper investigates the effect of water molecules' absorption on mechanical and thermal properties of polyamide6/hexagonal boron nitride (PA6/h-BN) composites.Design/methodology/approachThe PA6/h-BN composites were exposed to an open environment and water for 15 days to analyse the effect of humidity/water molecules' absorption on mechanical and thermal properties. The tensile strength, hardness and impact strength of materials were measured and compared. The scanning electron microscopy (SEM), x-ray diffraction (XRD) and differential scanning calorimetry (DSC) analyses were utilized to see the influence of water absorption on microstructure, crystallinity and glass transition temperatures.FindingsAfter exposing materials to an open environment and water, the tensile strength and hardness were found to decline, while improvement in impact strength was noticed. SEM characterization revealed the formation of voids/pockets in water-immersed materials. DSC analysis revealed the loss in glass transition temperatures, and XRD analysis revealed the loss in crystallinity of water-immersed materials.Originality/valueEnvironmental conditions vary according to the geographical areas, and it varies in many countries throughout the year. Polyamides are sensitive to the environmental humidity and can absorb a large amount of moisture from the environment. It becomes necessary to test these materials in their original working conditions, and sometimes it is mandatory to see the effects of extreme environmental conditions on a component. In this article, efforts have been made to investigate the influence of extreme humidity/water conditions on thermo-mechanical properties of PA6/h-BN composites.


2011 ◽  
Vol 217-218 ◽  
pp. 1606-1610
Author(s):  
Dong Jiang ◽  
Xiao Ran Zhang ◽  
Yan Mei Ma ◽  
Cheng You Ma

A series of random polysulfone/polyethersulfone (PSF/PES) copolymers were synthesized by the polycondensation of 4, 4'-isopropylidendiphenol, 4, 4΄-dihyolroxy diphenyl sulfone and 4, 4'-dichlorodiphenyl sulfone in the presence of K2CO3. We obtained a series of copolymers by changing the molar ratio of 4, 4΄-dihyolroxy diphenyl sulfone and 4, 4'-isopropylidendiphenol (it was marked as the ratio of S:A). The copolymers have the similar solubility with polyethersulfone. They also have high glass transition temperatures (Tg: 199°C~229°C) and 5% weight loss temperatures (4, 4'-isopropylidendiphenol: 4, 4΄-dihyolroxy diphenyl sulfone=1:1, Td5=497°C). At the same time the elongation at break is much higher than that of PES, while the tensile strength is a little lower than that of PES.


1966 ◽  
Vol 39 (4) ◽  
pp. 881-896 ◽  
Author(s):  
Joginder Lal ◽  
Kenneth W. Scott

Abstract The glass transition temperatures of high molecular weight poly (vinyl n-alkyl ethers) decrease with increasing length of the n-alkyl group. On lengthening the n-alkyl group, 14 per cent of the specific volume increase is free volume. Branching or substitution in the alkyl group of the polymer increases the Tg value. A comparison of poly (vinyl n-alkyl ethers) and polymers of normal α-olefins shows that an ether group and a methylene group in the side chain are equivalent in influencing the glass transition temperature. We have varied systematically the side chain alkyl group in poly (vinyl alkyl ethers) and evaluated at 3 different temperatures the influence of these variations on the dynamic properties of the vulcanizates of these polymers. The relative position of the curves, relating dynamic resilience to dynamic modulus of these polymers, is generally in the order of their glass transition temperatures. The dynamic mechanical property data on poly (vinyl n-pentyl ether) and poly (vinyl 2-ethylhexyl ether), which have the same glass transition temperature, fall on a common curve characteristic of the temperature of measurement. Apparently, the Tg is a major factor in correlating the dynamic mechanical behavior of these elastomers. The size and shape of the alkyl group appear to be reflected primarily in their effect on the Tg. Polysulfidic crosslinks are not essential for the attainment of high tensile strength in natural rubber vulcanizates cured with a sulfur-diphenylguanidine system. Data for the samples which had lost significant amounts of polysulfidic crosslinks by reaction with triphenylphosphine fitted a curve of tensile strength as a function of 300 per cent modulus for the control samples.


2017 ◽  
Vol 737 ◽  
pp. 262-268
Author(s):  
Hye Ryun Lee ◽  
Moon Il Kim ◽  
Hye Ryun Na ◽  
Choong Sun Lim ◽  
Bong Kuk Seo

Epoxy/silica composites were prepared using aminopropyl triethoxysilane (APTES)-modified silica nanoparticles in the sol state. Different sizes of silica particles were synthesized and they were applied into the epoxy/silica composites with different compositions. The mechanical and thermal properties of the composites were investigated and compared with those of pristine epoxy composite. The structure and morphology of the modified silica nanoparticles and epoxy/silica composites were analyzed using field emission scanning electron microscope. The flexural modulus and tensile strength of the epoxy/silica composites were investigated by universal test machine (UTM). Also, glass transition and thermal stability were investigated using thermomechanical analyzer (TMA). Sizes of silica particles in sol state were controlled by using different concentration of the accelerator. The tensile strength of epoxy/silica composites containing 20 wt% of 30 nm silica was found to be 37.98 MPa. In addition, the glass transition temperature (Tg) decreased with increasing silica particle sizes.


1989 ◽  
Vol 167 ◽  
Author(s):  
Paul R. Resnick

AbstractTeflon® AF is a family of amorphous fluoropolymers with glass transition temperatures as high as 300° based on bis-2,2-trfluoromethyl-4,5-difluoro-1,3-dioxole, (I), which has unusual properties [1–3] (Figure 1). The family retains the superior electrical, chemical resistance and thermal properties associated with fluoropolymers. In addition the polymers have high optical clarity, limited solubility in some commercially available perfluorinated ethers such as Fluorinert® FC-75 and improved physical properties below their glass transition temperatures (Figure 2). Teflon® AF polymers may be either solution cast into clear micron thin films or melt processed into a variety of forms.


2020 ◽  
Vol 44 (43) ◽  
pp. 18917-18928
Author(s):  
Ting Wang ◽  
Zhi-cheng Wang ◽  
Zhong-cheng Pan ◽  
Abdul Qadeer Dayo ◽  
Wen-bin Liu ◽  
...  

Poly(t-BF-sa-a) showed much better thermal properties and glass transition temperatures than traditional fluorene-based benzoxazine monomers.


2018 ◽  
Vol 762 ◽  
pp. 171-175 ◽  
Author(s):  
Lauma Laipniece ◽  
Valdis Kampars

We have synthesized polyester type dendrimers containing azobenzene chromophore in the core and trityl groups at the periphery using divergent growth strategy up to 3rdgeneration. We analyzed dendrimer samples using NMR, HPLC, TG, DSC and UV-Vis techniques. We found out that functionalization of dendrimer periphery is not complete. Dendrimers with trityl groups at the periphery have glass transition temperatures in the range 73-87 °C.


1998 ◽  
Vol 10 (1) ◽  
pp. 1-10 ◽  
Author(s):  
S Tamai ◽  
W Yamashita ◽  
A Yamaguchi

1, 3-Bis(3-aminobenzoyl)benzene (BAB), 1, 3-bis(3-amino-4-phenoxybenzoyl)benzene (BAPB) and 1, 3-bis(3-amino-4-biphenoxybenzoyl)benzene (BABB) were synthesized from 1, 3-bis(3-nitro-4-chlorobenzoyl)benzene. By using these three diamines and commercially available tetracarboxylic dianhydrides such as 3, 3′, 4, 4′-benzophenone tetracarboxylic dianhydride (BTDA) and pyromellitic dianhydride (PMDA), several kinds of poly(keto-imide)s were synthesized. Thermal properties and processability such as melt-flowability and solubility in organic solvents of the obtained poly(keto-imide)s were investigated by focusing on the chemical structures of their repeating structure units. Inherent viscosities of poly(keto-imide)s ranged from 0.54 to 0.75 dl g−1. These poly(keto-imide)s displayed glass transition temperatures ( Tg) between 219 and 256 °C, and only the poly(keto-imide) prepared from BAB and PMDA showed a melting point ( Tm)at 451 °C. Melt-flowabilities of these poly(keto-imide)s except for BAB/PMDA poly(keto-imide) were observed between 285 and 330 °C. The poly(keto-imide)s having bulky pendent ether groups were soluble in chloroform, 1, 1, 2-trichloroethane, N, N-dimethylacetamide and m-cresol at ambient temperature.


2008 ◽  
Vol 8 (9) ◽  
pp. 4797-4802 ◽  
Author(s):  
Yoon-Mi Lee ◽  
Soo-Kang Kim ◽  
Chang-Jun Lee ◽  
Ji-Hoon Lee ◽  
Jong-Wook Park

This paper reports a new HTL material that has high glass-transition temperatures (Tg) and excellent thermal properties. The synthesized material was N,N-diethyl-3,3′-bicarbazyl (DEBC), N,N-diphenyl-3,3′-bicarbazyl (DPBC) and N,N-dinaphthyl-3,3′-bicarbazyl (DNBC). The device that used DPBC as HTL showed the highest efficiency of 4.95 cd/A and 2.22 lm/W at 10 mA/cm2. This is an improvement by more than 10% from the luminance efficiency of NPB, a commercialized material.


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