Thermal and Mechanical Properties of Natural Rubber/Rice Starch Interpenetrating Network Hydrogel

2013 ◽  
Vol 844 ◽  
pp. 77-80
Author(s):  
Warisada Sila-On ◽  
Jatuporn Pratoomted ◽  
Utsana Puapermpoonsiri ◽  
Chaiwute Vudjung ◽  
Wiwat Pichayakorn
Keyword(s):  
Mechanical Properties ◽  
Natural Rubber ◽  
Mechanical Strength ◽  
Natural Rubber Latex ◽  
Amorphous Structure ◽  
Mechanical Tests ◽  
Rice Starch ◽  
Thermal And Mechanical Properties ◽  
Interpenetrating Networks ◽  
Scanning Calorimetry

Novel hydrogels based on natural rubber latex (NRL) and rice starch (RSt) (1:2 ratio) were prepared with various amount of N,N-methylenebisacrylamide (MBA) and 2.5 phr of maleic acid to form interpenetrating networks (IPN) using free-radical polymerization technique. The thermal and mechanical properties were performed by differential scanning calorimetry and mechanical tests. From data obtained, the change in Tg of rubber and melting point of RSt indicated that polymer-polymer interaction could be formed in IPN hydrogel. The higher amount addition of MBA created more mechanical strength of IPN hydrogels caused by the higher of interlacement formation. However, their mechanical strength of such hydrogels was lower than that of NRL alone due to the formation of amorphous structure in IPN hydrogel. These IPN hydrogels also improved the swelling property which will be utilized for wound healing application.

Study on Thermal and Mechanical Properties of Natural Rubber Latex Modified by Trichlorobromomethane

2011 ◽  
Vol 295-297 ◽  
pp. 36-40
Author(s):  
Xiao Xue Liao ◽  
Shuang Quan Liao ◽  
Bing Tang ◽  
Ming Chao Luo ◽  
Yan Fang Zhao ◽  
...  
Keyword(s):  
Natural Rubber ◽  
Storage Modulus ◽  
Loss Modulus ◽  
Natural Rubber Latex ◽  
Mechanical Analysis ◽  
Thermal And Mechanical Properties ◽  
Rubber Latex ◽  
Scanning Calorimetry ◽  
And Storage ◽  
Thermal Stability Of

Natural rubber latex (NRL) modified by holgonated addition with trichlorobromomethane was prepared. The thermal properties of modified NRL were analyzed by thermogravimetric analysis (TG/DTG),differential scanning calorimetry (DSC) and dynamic mechanical analysis(DMA). The results showed that the thermal stability of modified NRL was lower than NRL and the thermal degradation of modified NRL was two-stage decomposition. With increasing of stress frequency, loss modulus and storage modulus of latex increased,while loss modulus and storage modulus of modified latex decreased,compared with NRL.

scholarly journals Thermal and Mechanical Assessment of PLA-SEBS and PLA-SEBS-CNT Biopolymer Blends for 3D Printing

2021 ◽  
Vol 11 (13) ◽  
pp. 6218
Author(s):  
Balázs Ádám ◽  
Zoltán Weltsch
Keyword(s):  
Mechanical Properties ◽  
3D Printing ◽  
Mechanical Tests ◽  
The Other ◽  
Raw Material ◽  
Bending Test ◽  
Thermal And Mechanical Properties ◽  
Scanning Calorimetry ◽  
Partial Fracture ◽  
The Impact

Polylactic acid (PLA) is one of the most promising biopolymers often used as a raw material in 3D printing in many industrial areas. It has good mechanical properties, is characterized by high strength and stiffness, but unfortunately, it has some disadvantages; one is brittleness, and the other is slow crystallization. Amounts of 1–5% SEBS (styrene-ethylene-butylene-styrene) thermoplastic elastomer were blended into the PLA and the thermal and mechanical properties were investigated. DSC (Differential Scanning Calorimetry) measurements on the filaments have shown that SEBS increases the initial temperature of crystallization, thereby acting as a nucleating agent. The cooling rate of 3D printing, on the other hand, is too fast for PLA, so printed specimens behave almost amorphously. The presence of SEBS increases the impact strength, neck formation appears during the tensile test, and in the bending test, the mixture either suffers partial fracture or only bends without fracture. Samples containing 1% SEBS were selected for further analysis, mixed with 0.06 and 0.1% carbon nanotubes (CNTs), and tested for thermal and mechanical properties. As a result of CNTs, another peak appeared on the DSC curve in addition to the original single-peak crystallization, and the specimens previously completely broken in the mechanical tests suffered partial fractures, and the partially fractured pieces almost completely regained their original shape at the end of the test.

scholarly journals Effects of Kaolin Surface Treatments on the Thermomechanical Properties and on the Degradation of Polypropylene

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Melia Guessoum ◽  
Sorya Nekkaa ◽  
Françoise Fenouillot-Rimlinger ◽  
Nacerddine Haddaoui
Keyword(s):  
Mechanical Properties ◽  
Ammonium Salt ◽  
Silane Coupling Agent ◽  
Weak Interactions ◽  
Mechanical Tests ◽  
Thermomechanical Properties ◽  
Thermal And Mechanical Properties ◽  
Initial State ◽  
Scanning Calorimetry ◽  
Silane Coupling

The effects of kaolin content and treatments on the thermal and mechanical properties and on the degradation of polypropylene were examined using mechanical tests, differential scanning calorimetry (DSC), and thermogravimetry (TGA). The weak interactions filler/matrix have been reinforced using a modification with urea then with an ammonium salt and a surface treatment with a silane coupling agent. The XRD results showed that the peak at thed-value of 10.7 Å increases in urea/kaolin complex, but the treatment with the ammonium salt caused the return to the initial state of the clay. FTIR results showed the appearance of new bands characteristic of the interactions between urea and kaolinite and the alkylammonium and kaolinite. The mechanical properties of the composites exhibited important variations while the DSC results showed the decrease of the crystallization temperature as a function of kaolin content. TGA thermograms pointed out the improvement of the composites' thermal stability.

Fabrication of Novel Polyhydroxybutyrate-co-Hydroxyvalerate (PHBV) Mixed with Natural Rubber Latex

2015 ◽  
Vol 659 ◽  
pp. 404-408 ◽  
Author(s):  
Karndarthip Kuntanoo ◽  
Sarunya Promkotra ◽  
Pakawadee Kaewkannetra
Keyword(s):  
Mechanical Properties ◽  
Natural Rubber ◽  
Testing Machine ◽  
Natural Rubber Latex ◽  
Melting Behavior ◽  
Melting Transition ◽  
Rubber Latex ◽  
Scanning Calorimetry ◽  
Wide Range ◽  
Mixed Films

Polyhydroxybutyrate-co-hydroxyvalerate (PHBV) is mixed with natural rubber latex to make better mechanical properties of PHBV. The various ratios between PHBV and natural rubber latex are examined to improve their mechanical properties. The PHBV are solid, easily broken, while natural rubber is excessive elastic materials. Concentrations of the employed PHBV solution are 1, 2, and 3 (%w/v). The mixtures of this solution to natural rubber latex are fabricated the biofilms in three different ratios, 4:6, 5:5, and 6:4, respectively. The films are characterized by electron microscope, universal testing machine, and differential scanning calorimetry (DSC). The electron micrographs of the mixed films and unmixed PHBV yield the lowest void distributions in 3%w/v PHBV. For mechanical properties, the averaged elastic moduli of 1, 2, and 3 (%w/v PHBV) mixed films are 773, 955 and 1,008 kPa, respectively. Their tensile strengths increase with increasing the PHBV concentrations. A similar trend is also found in elastic modulus. The crystallization and melting behavior of pure PHBV and the mixed films are examined by DSC. Melting transition temperatures of pure PHBV exhibit two melting peaks at 154°C and 173°C. In addition, the melting peaks of the mixed films remain in the range of 152-156°C and 168-171°C, respectively. According to their morphology, void distributions reduce twice, compared to the unmixed PHBV. Mechanical properties and thermal analysis indicate that the mixed PHBV can be improved their properties with more resilient and wide range temperature than usual.

scholarly journals Investigation of the Effects of Titanate as Coupling Agent and Some Inorganic Nanoparticles as Fillers on Mechanical Properties and Morphology of Soft PVC

2011 ◽  
Vol 2011 ◽  
pp. 1-9 ◽  
Author(s):  
Morteza Hajian ◽  
Gholam Ali Koohmareh ◽  
Afsaneh Mostaghasi
Keyword(s):  
Mechanical Properties ◽  
Coupling Agent ◽  
Mechanical Tests ◽  
Inorganic Nanoparticles ◽  
Nano Particles ◽  
Thermal And Mechanical Properties ◽  
Scanning Calorimetry ◽  
Nanoscale Particles ◽  
The Impact ◽  
Thermal Stability Of

The effects of titanate as a coupling agent and some particulate nanoscale particles such as TiO2, CaCO3, and ZnO on thermal and mechanical properties of emulsion polyvinylchloride (E-PVC) were investigated by thermogravimetric analysis (TGA), and mechanical tests. In this research, it was found that, in the presence of nanoparticles of CaCO3, TiO2, and ZnO, the peak temperature of dehydrochlorination of E-PVC was shifted to higher temperatures, and the rate of mass loss was decreased. Also results of differential scanning calorimetry showed that the addition of nanoparticle of CaCO3, TiO2, and ZnO led to an increase in glass transition temperature. The impact strength, elastic modulus and toughness of the samples were enhanced after addition of 0–10 part of filer in hundred parts of resin (phr) nano-CaCO3, nano-TiO2, and nano-ZnO due to improvement of compatibility of the polymer and the nano-particles. Also UV and thermal stability of the samples were enhanced by means of the nanoparticles. It was found that, in the presence of titanate as coupling agent, content of additives that could be used in the composite of PVC shifts to higher amounts.

Structure and properties of a phenylethynyl-terminated PMDA-type asymmetric polyimide

2018 ◽  
Vol 31 (3) ◽  
pp. 261-272 ◽  
Author(s):  
Yixiang Zhang ◽  
Masahiko Miyauchi ◽  
Steven Nutt
Keyword(s):  
Mechanical Properties ◽  
Thermal Processing ◽  
Amorphous Structure ◽  
Decomposition Temperature ◽  
Thermal And Mechanical Properties ◽  
Chain Mobility ◽  
Amorphous Structures ◽  
The Cross ◽  
Imide Oligomers ◽  
The Relationship

A new polymerized monomeric reactant (PMR)-type polyimide, designated TriA X, was investigated to determine polymer structure, processability, thermal, and mechanical properties and establish the relationship between the molecular structure and those properties. TriA X is a PMR-type polyimide with an asymmetric, irregular, and nonplanar backbone. Both the imide oligomers and the cross-linked polyimides of TriA X exhibited loose-packed amorphous structures, independent of thermal processing. The peculiar structures were attributed to the asymmetric backbone, which effectively prevented the formation of closed-packed chain stacking typically observed in polyimides. The imide oligomers exhibited a lower melt viscosity than a control imide oligomer (symmetric and semi-crystalline), indicating a higher chain mobility above the glass transition temperature ( Tg). The cured polyimide exhibited a Tg = 362°C and a decomposition temperature = 550°C. The cross-linked TriA X exhibited exceptional toughness and ductility (e.g. 15.1% at 23°C) for a polyimide, which was attributed to the high-molecular-weight oligomer and loose-packed amorphous structure. The thermal and mechanical properties of TriA X surpass those of PMR-15 and AFR-PE-4.

Phase Morphology, Thermal and Mechanical Properties of Compatibilized Nylon12/Natural Rubber Blends Using PS/MNR

2013 ◽  
Vol 844 ◽  
pp. 53-56
Author(s):  
Saravalee Saengthaveep ◽  
Sadhan C. Jana ◽  
Rathanawan Magaraphan
Keyword(s):  
Mechanical Properties ◽  
Natural Rubber ◽  
Moisture Absorption ◽  
Rubber Particle ◽  
Impact Resistance ◽  
Phase Morphology ◽  
Thermal And Mechanical Properties ◽  
Binary Blend ◽  
Polyamide 12 ◽  
The Impact

To produce a tough material for application demanding high impact resistance and low moisture absorption, melt blending of Nylon12 (Polyamide 12, PA12) and natural rubber (NR) was carried out in a brabender plasticorder at 210 °C with rotor speed of 70 rpm in the presence of polystyrene/maleated natural rubber (PS/MNR) blend as a compatibilizer. The effect of compatibilizer content (1, 3, 5, 7 and 10 phr) on phase morphology, thermal, and mechanical properties of [Nylon12/NR]/[PS/MNR] blends was investigated by using SEM, DSC, and Izod impact tester, respectively. The result revealed that PS/MNR blend improved the compatibility of Nylon12/NR blends efficiently due to the presence of amide linkage at the interfaces from the reaction between the reactive groups of MNR and the NH2 end groups of Nylon12 during mixing. A fine phase morphology (good dispersion and small dispersed phase size of NR domains in Nylon12 matrix) of [Nylon12/NR]/[PS/MNR] blends was observed at the optimum compatibilizer content of 7 phr, relating to the improvement of mechanical property. The impact energy of [Nylon12/NR]/[PS/MNR] blends was 503 J/m higher than that of neat Nylon12 (115 J/m) and Nylon12/NR binary blend (241 J/m) due to the toughening effect of rubber and proper morphology. The melting temperature of all blends did not change obviously from thermal analysis. However, the presence of rubber particle obstructed the crystallization of Nylon12 phase, leading to the decreasing of %crystallinity from 93% to around 70%.

Effects of Steam Heat and Dry Heat Sterilization on Thermal and Mechanical Properties of Nylon and Policarbonate in Fabrication with Fused Filament

2021 ◽  
Vol 891 ◽  
pp. 150-163
Author(s):  
Jorge Mauricio Fuentes ◽  
Omar Flor Unda ◽  
Santiago Ferrandiz ◽  
Franyelit Suarez
Keyword(s):  
Mechanical Properties ◽  
Thermomechanical Analysis ◽  
Mechanical Tests ◽  
Effect Of Temperature ◽  
Mechanical And Thermal Properties ◽  
Scanning Calorimetry ◽  
Thermal Tests ◽  
Dry Heat ◽  
Izod Impact ◽  
Steam Heat

In this article presents evidence about performance of mechanical properties of polycarbonate and nylon materials, which are used in the additive manufacturing by deposition of molten material and that have been subjected to sterilization processes by moist heat at 121°C and dry heat at 140°C. This study provides useful information to consider the use of these materials in sanitary and sterile settings. Mechanical tests of tensile, flex, hardness, Izod impact, thermal tests in Differential Scanning Calorimetry DSC, Thermomechanical analysis TMA and Scanning Electron Microscopy SEM were performed. It is concluded that the mechanical and thermal properties have not been altered through the effect of temperature in sterilization processes.

scholarly journals Simultaneous Enhancement of Strength and Toughness of PLA Induced by Miscibility Variation with PVA

Polymers ◽  
2018 ◽  
Vol 10 (10) ◽  
pp. 1178 ◽  
Author(s):  
Yanping Liu ◽  
Hanghang Wei ◽  
Zhen Wang ◽  
Qian Li ◽  
Nan Tian
Keyword(s):  
Mechanical Properties ◽  
High Performance ◽  
Fracture Strain ◽  
Electrospun Fiber ◽  
Structural Evolution ◽  
Amorphous Structure ◽  
Poly Lactic Acid ◽  
Poly Vinyl Alcohol ◽  
Scanning Calorimetry ◽  
Strength And Toughness

The mechanical properties of poly (lactic acid) (PLA) nanofibers with 0%, 5%, 10%, and 20% (w/w) poly (vinyl alcohol) (PVA) were investigated at the macro- and microscale. The macro-mechanical properties for the fiber membrane revealed that both the modulus and fracture strain could be improved by 100% and 70%, respectively, with a PVA content of 5%. The variation in modulus and fracture strain versus the diameter of a single electrospun fiber presented two opposite trends, while simultaneous enhancement was observed when the content of PVA was 5% and 10%. With a diameter of 1 μm, the strength and toughness of the L95V5 and L90V10 fibers were enhanced to over 3 and 2 times that of pure PLA, respectively. The structural evolution of electrospun nanofiber was analyzed by differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR). Although PLA and PVA were still miscible in the concentration range used, the latter could crystallize independently after electrospinning. According to the crystallization behavior of the nanofibers, a double network formed by PLA and PVA—one microcrystal/ordered structure and one amorphous structure—is proposed to contribute to the simultaneous enhancement of strength and toughness, which provides a promising method for preparing biodegradable material with high performance.

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