Study of morphological and mechanical properties of PP/PBT blends

Summary The synthesis of emulsifiers has been performed by the condensation of terephthaloyl chloride, butanediol and hydrogenated - hydroxy polyisoprenes. The products are carefully characterized by ¹H-nuclear magnetic resonance (NMR), infra-red spectroscopy and size exclusion chromatography.The PP/PBT blend, in a 60:40 ratio, was prepared with, and without, emulsifiers by melt-blending. The effect of these emulsifiers on mechanical properties and morphological studies of the PP/PBT blend was examined.     

Solid state features and mechanical properties of PEI/PBT blends

Extrusion‐blended and injection‐molded PEI/PBT blends were found to be miscible whatever the composition. The processability of the blends clearly improved with the presence of PBT. The melt pressure at the exit was seen to be a parameter as representative of the processability of the blends as the torque of blending. In the blends with 80 and 90% PBT, a positive volume of mixing and the maintenance of the crystallinity of PBT were seen. However, in the rest of the blends, negative volumes of mixing and important decreases in the crystallinity of PBT were found. These solid state features gave rise to a ductility similar to that of the pure PEI and to a synergism of the modulus of elasticity and of the yield stress in the 90/10 and 80/20 blends such that the values were higher than those of either of the pure components. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 885–892, 2001     

Polyarylene ether nitrile/divinyl siloxane-bisbenzocyclobutene composite films: Curing reaction and thermal/mechanical/dielectric properties

Polymer dielectrics, are commonly used as insulating materials for electronic products. Light weight, good mechanical properties and high thermal conductivity are important properties. However, electrical and thermal parameters are interrelated, and it is challenging to have a dielectric polymer that is also resistant to high temperatures and high thermal conductivity. Hence, high-performance composite films were prepared by the method of post-solid phase chemical reaction using polyarylene ether nitrile (PEN) and divinyl siloxane-bisbenzocyclobutene (BCB) as raw materials. First, parameters of the curing reaction were determined by rheological and activation energy calculations. Then, through adjusting the content of BCB resin and treatment temperature, the performance of PEN/BCB composites could be tuned. Thermal properties have been studied by differential scanning calorimetry, dynamic mechanical analysis, thermal gravimetric analysis, and hot-disk method. Here, the PEN/BCB composite electric insulating materials with outstanding thermal performance (T_g: 208–400°C, T_5%: 469–544°C, thermal conductivity: 1.270–2.215 W/m K). Besides, its mechanical and dielectric properties were investigated in detail. It is noteworthy that the tensile strength of composite film can exceed a maximum of 130 MPa, which is 23.19% higher compared to the untreated one. Also, PEN/BCB composites own low dielectric constant (2.27–4.08 at 1 KHz), and the relationship between frequency or a wide temperature range and dielectric constant/loss is stable. Thus, it has a greater potential for applications in electronics in high-temperature environments.     

Mechanical and dielectric breakdown properties of PBT/TPE,PBT/PBT/PET,and PBT/antioxidant blends

To improve the thermal aging flexibility of poly(butylene terephthalate) (PBT), PBT was melt‐blended with three type thermoplastic elastomer [poly ether‐ester type (TPE1), polyester‐ester type (TPE2), and poly(buthylene 2,6‐naphthalate)/poly(tetramethylene glycol) block copolymer type (TPE3)], PBT/poly(ethylene terephthalate), (PET) alloy (Alloy), and phosphate type antioxidant (T1). The content of the three type TPEs and Alloy was fixed at 20 parts per 100 g of PBT. The morphology and thermal behavior of these blends have been investigated with scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and thermogravimetry (TG). In the case of PBT/Alloy‐20 and PBT/TPE3–20 blends show clean fractured surface, whereas for PBT/TPE1–20 and PBT/TPE2–20 blends, the elongated pieces or fiber can be seen abundantly which indicates a good compatibility. TG traces show a significant shift of the weight loss toward higher temperature for PBT/Alloy‐20, whereas PBT/TPE1–20, PBT/TPE2–20 and PBT/TPE3–20 blend decrease in thermal stability than PBT. To investigate the applicability for insulation material, the prepared blend samples were extruded an electric wire and flexibility and electric breakdown voltage (BDV) of wire after thermal aging were studied. For PBT/TPE1–20 and PBT/TPE2–20 blends did not show any cracks after flexibility test at 130°C for 6 h and 225°C for 30 min. In contrast PBT, PBT/Alloy‐20, PBT/TPE3–20, and PBT/T1–1 showed a partial crack in the insulation after flexibility test at 130°C for 6 h although its good flexibility at 225°C for 30 min. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Morphology,mechanical, and dielectric breakdown properties of PBT/PET/TPE,PBT/PET/PA66, PBT/PET/LMPE,and PBT/PET/TiO2 blends

The morphology and thermal behavior of tertiary blends of poly(butylene terephthalate) [PBT]/poly(ethylene terephthalate) [PET] alloy resin (Alloy)/thermoplastic elastomer (TPE), Alloy/nylon 66 (PA66), Alloy/low molecular weight polyester (LMPE), and Alloy/titanium dioxide (TiO₂) have been investigated by scanning electron microscopy, differential scanning calorimetry, and thermogravimetry (TG). In case of TPE and LMPE containing blends did not show any morphological change compared with Alloy whereas for PA66 containing blends, the size of the dispersed phase increased with the increase the PA66 contents. The crystallization peak of Alloy/TPE blends became undetectable with an increasing TPE content. In contrast, the crystallization temperature (T_c1) of Alloy/PA66, Alloy/LMPE, Alloy/TiO₂ blends increased significantly as the PA66, LMPE, and TiO₂ content increases. TG traces show a significant shift of the weight loss towards higher temperature for Alloy/TiO₂ blend whereas Alloy/TPE, Alloy/PA66 and Alloy/LMPE blends slightly decreases in thermal stability than Alloy. To investigate the applicability for insulation material, the prepared blend samples were extruded an electric wire and the breakdown voltage (BDV) of wires was investigated. The melt flow rate of Alloy increased as the amount of TPE increased, and a contrary trend was found when the increase of the amount of TiO₂. The dielectric breakdown test applies a voltage that is greater than the product's rated operating voltage for a specific period of time during which dielectric breakdown must not occur. The BDV of Alloy/TPE and Alloy/PA66 blends is higher than other blends before and after thermal aging 225°C for 30 min. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers     

Studies on blends of binary crystalline polymers: Miscibility and crystallization behavior in PBT/PAr(I27-T73)

The miscibility and crystallization behavior of binary crystalline blends of poly(butylene terephthalate) [PBT] and polyarylate based on Bisphenol A and a 27/73 mole ratio of isophthalic and terephthalic acids [PAr(I27-T73)] have been investigated by differential scanning calorimetry (DSC). This blend system exhibits a single composition-dependent glass transition temperature over the entire composition range. The equilibrium melting point depression of PBT was observed, and Flory interaction parameter χ₁₂ = −0.96 was obtained. These indicate that the blends are thermodynamically miscible in the melt. The crystallization rate of PBT decreased as the amount of PAr(I27-T73) increased, and a contrary trend was found when PAr(I27-T73) crystallized with the increase of the amount of PBT. The addition of high-T_g PAr(I27-T73) would suppress the segmental mobility of PBT, while low-T_g PBT would have promotional effect on PAr(I27-T73). The crystallization rate and melting point of PBT were significantly influenced when the PAr(I27-T73) crystallites are previously formed. It is because not only does the amorphous phase composition shift to a richer PBT content after the crystallization of PAr(I27-T73), but also the PAr(I27-T73) crystal phase would constrain the crystallization of PBT. Thus, effects of the glass transition temperature, interaction between components, and previously formed crystallites of one component on the crystallization behavior of the other component were discussed and compared with blends of PBT and PAr(I-100) based on Bisphenol A and isophthalic acid.     

PBT/PET conjugated fibers: Melt spinning,fiber properties,and thermal bonding

This work examines the PBT/PET sheath/core conjugated fiber, with reference to melt spinning, fiber properties and thermal bonding. Regarding the rheological behaviors in the conjugated spinning, PET and PBT show the smallest difference between their melt‐viscosity at temperatures of 290°C and 260°C respectively, which has been thought to represent optimal spinning conditions. The effect of processing parameters on the crystallinity of core material‐PET was observed and listed. In order of importance, these factors are the draw ratio, the heat‐set temperature, and the drawing temperature. The crystallinity of sheath material‐PBT, however, can be considered to be constant, independent of any processing parameters. The bulk orientation, rather than the crystallinity of PET core, dominates the tenacity of PBT/PET sheath/core fiber. Moreover, heat‐set treatment after drawing is recommended to yield a highly oriented conjugated fiber. With respect to thermal bonding, PBT/PET conjugated fibers processed via high draw ratio but low‐temperature heat setting can form optimal thermal bonds at a constant bonding temperature of 10°C above the T_m of PBT.     

Influence of polyhedral oligomeric silsesquioxanes on thermal and mechanical properties of polycarbonate/POSS hybrid composites

Two types of silsesquioxanes were synthesized by hydrolytic condensation reaction, and then were incorporated into polycarbonate (PC) matrix by melt blending to prepare PC/POSS hybrid composites. The study of morphology of the composites showed that octaphenylsilsesquioxane (PH‐POSS) exhibited partial compatibility with PC matrix, while 3‐glycidyloxypropylsilsesquioxane (EP‐POSS) could react with phenolic hydroxyl groups of matrix. Thermal and mechanical properties were studied by DSC, TGA, and DMA. The result showed that the incorporation of POSS not only improved thermal stabilities of PC composites, but also retarded their thermal degradation. Si O fractions left during POSS degradations were the key factor governing the formation of a gel network layer on the exterior surface. This layer possessed more compact structures, higher thermal stabilities, and some thermal insulation. In addition, percentage residues at 700°C (C₇₀₀) significantly increased from 10.8 to 15.5–22.8% in air. The storage modulus of two series of composites was slightly improved up to 90°C; furthermore, the temperature range of the rubbery state of them shifted to high temperature. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

填料表面处理对ABS/CaCO3复合材料性能的影响

在室温下,测定了CaCO3填充丙烯腈-丁二烯-苯乙烯三元共聚物(ABS)复合材料的力学性能。结果表明,随着CaCO3质量分数[W(CaCO3)]的增加,试样的拉伸弹性模量呈非线性提高,而拉伸强度和拉伸断裂能下降。当ω(CaCO3)小于10％时,试样的简支梁缺口冲击强度随着ω(CaCO3)的增加而迅速减小,而弯曲强度却增大,ω(CaCO3)达10％后两者均缓慢地减小。CaCO3的表面处理及其粒径大小对上述力学性能的影响不太明显。此外,测量了试样的维卡软化温度(TVC）,TVC随着ω(CaCO3)的增加而提高,这表明填充CaCO3粒子有利于改善ABS的耐热性能。     

Influence of the molecular weight on the thermal and mechanical properties of ethylene/norbornene copolymers

A series of ethylene‐norbornene copolymers were synthesized using Me₂Si(Me₄Cp)(NtBu)TiCl₂ as the metallocene catalyst and methylaluminoxane (MAO) as the cocatalyst, with the same molecular characteristics except the molecular weight, to evaluate its influence on the determination of the glass transition temperature (T_g). The polymers were characterized using wide‐angle X‐ray scattering, differential scanning calorimetry, microhardness measurements, and dynamic mechanical thermal analysis. The value of the T_g, for the same norbornene content and determined from the last three mentioned methods, increases significantly up to a limit of M_n about 6–10 × 10⁴ (g/mol). Above this value, T_g remains practically constant. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3358–3363, 2003     

Binary mixtures of polyethylene and oxidized wax: Dependency of thermal and mechanical properties upon mixing procedure

The influence of the preparation procedure on the thermal and mechanical properties of linear low‐density polyethylene (LLDPE)– and LDPE–oxidized wax blends was investigated. It was found that mechanically mixed blends show reduced thermal stability as well as ultimate mechanical properties (stress and strain at break) compared to that of extrusion mixed blends. However, the structure of the blend and consequently its thermal and mechanical behavior also depend on the initial morphology of polyethylene. DSC measurements show miscibility up to high wax contents in both blend types, but increasing the amount of wax in LDPE blends induces increasing crystallinity. As a result, the LDPE/wax blends show improved thermal stability of between 20 and 50°C at low wax concentrations. Although the elasticity modulus of the blends increases, increasing the amount of wax generally degrades the mechanical properties. The main reason for this is the reduced number of tie chains. Changes in the average concentration of tie chains with increasing wax content were calculated and a correlation was made with the ultimate properties of the blends. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2446–2456, 2003     

Polyimide/POSS nanocomposites: interfacial interaction, thermal properties and mechanical properties

A series of functional polyhedral oligomer silsesquioxnae (POSS)/polyimide (PI) nanocomposites were prepared using a two-step approach, first, the octa(aminophenyl)silsesquioxane (OAPS)/NMP solution was mixed with polyamic acid (PAA) solution prepared by reacting 4,4′-diaminodiphenylmethane and 3,3′,4,4′-benzophenonetetracarboxylic dianhydride in NMP, and second, the polycondensation solution was treated by thermal imidization. The well-defined ‘hard particles’ (POSS) and the strong covalent bonds between the PI and the ‘hard particles’ lead to a significant improvement in the thermal mechanical properties of the resulting nanocomposites. The glass transition temperature dramatically increases while the coefficient of thermal expansion (CTE) decreases, owing to the significant increase of the cross-linking density in the PI-POSS nanocomposites. The thermal stability and mechanical property of the nanocomposites were also improved.     

Structural and thermal behavior of PC/PBT blends

Blends of polycarbonate (PC) with poly(butylene terphthalate) (PBT) were characterized using density measurements, DSC, IR, and TGA. Addition of PBT increases the density values of blends linearly. All the blends show a single glass transition temperature, indicating the miscibility of the two polymers in the amorphous phase. With more than 6% addition of PBT to PC, PBT crystallizes as per its own crystal structure. The addition of 4% PBT to PC improves the thermal stability at higher temperature than does pure PC. IR studies shows that addition of PBT improves the intermolecular forces in PC, in particular, on the endgroup and the C? CH₃ and C?O groups as indicated in the frequencies 1020, 1370, and 1770–1790 cm^?1. © 1995 John Wiley & Sons, Inc.     

Influence of phosphorous-based flame retardants on the mechanical and thermal properties of recycled PC/ABS copolymer blends

The effects of three commercial aryl phosphate flame retardants (FRs; bisphenol A bis(diphenyl diphosphate) [BDP], triphenyl phosphate (TPP), and a proprietary oligomeric phosphate ester (OPE)) and a compatibilizer (methacrylate-butadiene-styrene copolymer [MBS]) on the thermal and mechanical properties of FR-recycled PC/acrylonitrile-butadiene-styrene copolymer (r-PC/r-ABS) blends are investigated. The addition of FRs to r-PC/r-ABS blends increases the storage, tensile, and flexural moduli, indicating a reinforcing effect. However, at elevated temperatures, FRs reduce the glass transition temperature and act as plasticizers. The thermal stability of r-PC/r-ABS/FR blends at 10% mass loss increases in the following order: r-PC/r-ABS/TPP < r-PC/r-ABS/BDP < r-PC/r-ABS/OPE < r-PC/r-ABS/OPE/MBS. Kinetics of thermal decomposition of the FR r-PC/r-ABS blends is studied calculating the thermal decomposition activation energies by the Flynn–Wall–Ozawa method. Scanning electron microscopy shows that r-PC/r-ABS/OPE blend is only partly miscible, while homogeneous structure is formed in the r-PC/r-ABS/OPE/MBS blend, which is supported by its good mechanical and thermal properties. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48377.     

In situ hot pressing/reaction synthesis,mechanical and thermal properties of Lu2SiO5

Lu₂SiO₅ is a promising candidate of environmental barrier coatings (EBC) for silicon based ceramics due to its excellent high temperature stability. However, little information is available for the mechanical and thermal properties of Lu₂SiO₅, which frustrated evaluation of its performances for EBC applications. In this paper, dense Lu₂SiO₅ ceramic is successfully fabricated from Lu₂O₃ and SiO₂ powders by in situ hot pressing/reaction sintering at 1500 °C. Mechanical properties, including Young's modulus, bulk modulus, shear modulus, Poisson's ratio, fracture toughness, Vickers hardness, and bending strength are reported for the first time. Lu₂SiO₅ possesses excellent high temperature mechanical properties up to at least 1300 °C. Thermal stress for the case of Lu₂SiO₅ or Y₂SiO₅ coating on silicon bond coat and thermal stress resistance parameter are also estimated based on the experimental mechanical and thermal properties. The present results suggest that Lu₂SiO₅ has better reliability than Y₂SiO₅ in harsh thermal environment.     

Influence of blocked polyisocyanate on the mechanical, thermal and interfacial properties of bamboo/hydroxyl-terminated polyurethane composites

In this study, chemical modification of bamboo powder (BP)/hydroxyl-terminated polyurethane (HPU) composites obtained by hot press was investigated using blocked polyisocyanate synthesized from reaction of isophorone diisocyanate with 1,1,1-trimethylolpropane (TMP) followed by addition of methyl ethyl ketoxime (MEKO). The modified surface of MEKO-blocked polyisocyanate (M-bp)-treated BP/HPU composites was identified by Fourier transform infrared spectroscopy from the appearance of CO bands absorbance and the reduction in relative intensity of OH, with respect to bamboo. The effects of M-bp as a cross-linker on the properties of the products were studied. Mechanical testing results showed that the tensile and flexural properties of the composites were improved by addition of such a cross-linker. The morphology analysis revealed that the M-bp-modified composites exhibited better compatibility and homogeneous morphologies in comparison with the unmodified composites. Moreover, the thermogravimetric analysis demonstrated that thermal resistance of the composites was enhanced by addition of M-bp. The moisture absorption characteristics of the products were also studied and discussed, because it is a major influencing factor for natural fibre composites. The results showed that better water resistance of modified composites was obtained due to stronger interfacial adhesion. Based on the findings in this work, they all indicated that the chemical modification occurred by the cross-linking effect of M-bp, which induced the strong bonds among the composite components.     

Influence of molecular weight on rheological,thermal, and mechanical properties of PEEK

This study focuses on the influence of molecular weight on the rheological, thermal, and mechanical behavior of poly(ether‐ether‐ketone) (PEEK), a semicrystalline high‐performance polymer. The results show that the molecular weight of PEEK has significant influence on its rheological, thermal, and mechanical behavior. It was found that PEEK has the unique characteristic of two shear‐thinning regions. The shear viscosity and the stress relaxation time of PEEK increase significantly as molecular weight increases. In general, the Cox‐Merz rule is valid for all grades of PEEK. As molecular weight increases, the melting temperature of PEEK decreases slightly, but its isothermal and nonisothermal crystallization temperatures drop dramatically. As molecular weight increases, the crystallinity, the crystallization rate, and the magnitude of crystallization activation energy decrease. The crystallization kinetics study indicates that PEEK tends to form spherical crystalline structures, regardless of its molecular weight. As molecular weight increases, the tensile strength at yield, the tensile modulus, and the flexural modulus of PEEK decrease slightly, whereas the tensile strength at break, the tensile strain at break, the modulus of toughness, and the impact strength of PEEK increase significantly. POLYM. ENG. SCI., 2011. © 2010 Society of Plastics Engineers     

Influence of tragacanth resin on the thermal and mechanical properties of fly ash-cement composites

This study was aimed to search the possibility of usage of the thermal power plants fly ashes, cement and tragacanth composites in concrete or plaster by investigating their thermal insulation characteristics. The fly ash used in the experiments is supplied from Af?in Elbistan Thermal Power Station. Portland cement (KPC 325) with resin is used as binding and 24 specimens are prepared depending on the percentage of fly ash and tragacanth. In all fly ash, tragacanth and binding mixture, the weight percentages of fly ash are taken as 0, 10, 20, 30, 40 and 50%. The amount of the resin in the mixture is 0.5, 1 and 1.5% of the weight of the total cement and fly ash.

24 samples were prepared and tested to find out the effects of resin on thermal and mechanical properties of fly ash and cement composites. Whereas fly ash percentage increased from 0% to 50%, i) thermal conductivity and compressive strength decreased 19.37–28.62% and 7.66–16.55% respectively as the porosities of the samples increased 18.91–28.62% with the effect of artificial pores generated by 1.5% resin other than the pores generated by fly ash. ii) the new produced samples can be used as partition walls, floorings, ceiling concretes, briquettes or bricks and plaster.     

1,4-环己烷二甲醇改性PBT共聚酯的热性能研究

以对苯二甲酸(PTA)、1,4-丁二醇(BD)和1,4-环己烷二甲醇(CHDM)为主要原料,制备了一系列CHDM改性聚对苯二甲酸丁二醇酯(PBT)共聚酯。采用差式扫描量热仪(DSC)和热重分析仪(TGA)等分析方法测试了共聚酯的性能,研究了不同CHDM含量对共聚酯热性能和结晶性能的影响。结果表明:随CHDM含量的增加,共聚酯玻璃化转变温度逐渐升高;共聚酯的熔点先降低后升高,CHDM/PTA摩尔比为40%时熔点最低;随CHDM含量的增加,共聚酯的结晶性能逐渐减弱。     

Effect of mechanical activation on thermal explosion in Ni-Al mixtures

The effect of mechanical activation (MA) on thermal explosion in equimolar Ni-Al mixtures was studied by time-resolved XRD. MA was also found to increase the burning velocity and decrease the ignition temperature. Thermal explosion in non-activated Ni-Al mixtures was found to proceed via formation of liquid (melted) intermediate products, while that in the activated mixtures gave no liquid intermediates.