Natural rubber grafted poly(methyl methacrylate) as compatibilizer in 50/50 natural rubber/nitrile rubber blend

2016 ◽  
Vol 49 (5) ◽  
pp. 422-439 ◽  
Author(s):  
Supat Moolsin ◽  
Nattawud Saksayamkul ◽  
Adul Na Wichien
Keyword(s):  
Thermal Properties ◽  
Natural Rubber ◽  
Methyl Methacrylate ◽  
Graft Copolymers ◽  
Nitrile Rubber ◽  
Proton Nuclear Magnetic Resonance ◽  
Tensile Fracture ◽  
Resonance Spectroscopy ◽  
Scanning Calorimetry ◽  
Oil Resistance

The effects of graft copolymers applied as compatibilizers for natural rubber/nitrile rubber (NR/NBR) blends at 50/50 (w/w) on cure characteristics, mechanical properties, thermal properties, oil resistance, and morphology were investigated. The graft copolymers of methyl methacrylate (MMA) onto NR initiated by benzoyl peroxide (NR- g-PMMA<BPO>) and by potassium persulfate (NR- g-PMMA<PPS>) under emulsion polymerization were synthesized and used to compatibilize the blends. The structures of the copolymers were characterized by Fourier transform infrared spectroscopy and proton nuclear magnetic resonance spectroscopy. NR was blended with NBR via a two-roll mill at 70°C under the compatibilizer loading ranging from 0 to 10 parts per hundred of rubber (phr). The results showed that the tensile property and tear strength of the blends increased with the increasing amount of NR- g-PMMA<BPO> as a compatibilizer. Thermal aging determined in terms of tensile properties exhibited the smaller difference between before and after aging in an oven with the increasing compatibilizer loading. The morphology of the compatibilized NR/NBR vulcanizates was investigated by scanning electron microscopy of the tensile fracture surfaces, which exhibited the improvement of interfacial adhesion between the two rubber phases. The thermal properties of compatibilized NR/NBR vulcanizates were reported in terms of a glass transition temperature under differential scanning calorimetry and dynamic mechanical analysis. The incorporation of an appropriate amount of the compatibilizer into the blends apparently improved the oil resistance of NR. Among them, the blend filled with 7.5 phr of NR- g-PMMA<BPO> showed the lowest volume change in IRM 903 oil.

Influence of Reaction Conditions on the Properties of Nano-matrix Structure Formed by Graft-Copolymerization of Acrylonitrile onto Natural Rubber

2013 ◽  
Vol 844 ◽  
pp. 365-368 ◽  
Author(s):  
Kontapond Prukkaewkanjana ◽  
Seiichi Kawahara ◽  
Jitladda Sakdapipanich
Keyword(s):  
Mechanical Properties ◽  
Natural Rubber ◽  
Graft Copolymerization ◽  
Monomer Concentration ◽  
Proton Nuclear Magnetic Resonance ◽  
Resonance Spectroscopy ◽  
Matrix Structure ◽  
Oil Resistance ◽  
Wide Range ◽  
Initial Monomer

Natural rubber (NR) is one of the most important agriculture products of Thailand, which is an important material with unique and special characteristics used in wide range of applications such as mechanical properties, excellent strength, and elasticity. However, it is inferior in oil resistance due to the presence of hydrogen and carbon in its structure. This inherent drawback of NR has limited its application in industry. In order to expand the use of NR, this research is interested to improve the oil resistance of NR without loss of outstanding properties by grafting NR with acrylonitrile (AN) monomer to form the nano-matrix structure. The influences of the initial monomer concentration and initial initiator concentration were investigated. These effects on structure, mechanical properties and oil resistance properties were studied by Fourier transform infrared spectroscopy and proton nuclear magnetic resonance spectroscopy, tensile machine, and swelling in toluene, respectively. It was found that the tensile strength and oil resistance properties of graft copolymerization of AN onto NR increased with increasing the percentage grafting efficiency of acrylonitrile monomer.

Thermal properties of a series of tetrafunctional fluorene-based oxazines/P-a blends

2016 ◽  
Vol 29 (10) ◽  
pp. 1139-1147 ◽  
Author(s):  
Zi Sang ◽  
Tiantian Feng ◽  
Wenbin Liu ◽  
Jun Wang ◽  
Mehdi Derradji
Keyword(s):  
Thermal Stability ◽  
Differential Scanning Calorimetry ◽  
Thermal Properties ◽  
Mechanical Analysis ◽  
Proton Nuclear Magnetic Resonance ◽  
Primary Amines ◽  
Resonance Spectroscopy ◽  
High Glass Transition Temperature ◽  
Scanning Calorimetry ◽  
Good Thermal Stability

A new series of aniline and aniline-mixed tetrafunctional fluorene-based oxazine monomers were synthesized using 2,7-hydroxy-9,9-bis-(4-hydroxyphenyl) fluorene, paraformaldehyde, and primary amines (including aniline or aniline mixed with n-butylamine or n-octylamine composition). Fourier transform infrared spectroscopy and proton nuclear magnetic resonance spectroscopy were used to characterize the structure of the monomers. The copolymers were obtained by adding the monomers into a typical monofunctional polybenzoxazine (phenol-aniline-based benzoxazine). Differential scanning calorimetry, thermogravimetric analysis, and dynamic mechanical analysis were performed to study the thermal properties of the copolymers. The copolymers exhibited high glass transition temperature values (164–201°C). A good thermal stability was also obtained with a 5% weight loss temperature over 355°C and high char yields at 800°C (42–50%).

scholarly journals Structural and Thermal Properties of Ethylene-Norbornene Copolymers Obtained Using Vanadium Homogeneous and SIL Catalysts

Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2433
Author(s):  
Paweł Groch ◽  
Anna Bihun-Kisiel ◽  
Aleksandra Piontek ◽  
Wioletta Ochędzan-Siodłak
Keyword(s):  
Thermal Properties ◽  
Reactivity Ratio ◽  
Proton Nuclear Magnetic Resonance ◽  
Sequence Length ◽  
Resonance Spectroscopy ◽  
Scanning Calorimetry ◽  
Reaction Conditions ◽  
Copolymer Microstructure ◽  
Chain Termination Reaction ◽  
Catalyst Systems

The series of ethylene-norbornene (E-NB) copolymers was obtained using different vanadium homogeneous and supported ionic liquid (SIL) catalyst systems. The 13C and 1H NMR (carbon and proton nuclear magnetic resonance spectroscopy) together with differential scanning calorimetry (DSC) were applied to determine the composition of copolymers such as comonomer incorporation (CNB), monomer dispersity (MD), monomer reactivity ratio (re), sequence length of ethylene (le) and tetrad microblock distributions. The relation between the type of catalyst, reaction conditions and on the other hand, the copolymer microstructure, chain termination reaction analyzed by the type of unsaturation are discussed. In addition, the thermal properties of E-NB copolymers such as the melting and crystallization behavior, like also the heterogeneity of composition described by successive the self-nucleation and annealing (SSA) and the dispersity index (DI) were determined.

Thermal Properties and Morphology of Compatible Poly(ethylene oxide)/Natural Rubber-graft -poly(methyl methacrylate) Blends

2018 ◽  
Vol 382 (1) ◽  
pp. 1800083 ◽  
Author(s):  
Nurul F. A. Zainal ◽  
Margarethe Hein ◽  
Volker Abetz ◽  
Ab M. M. Ali ◽  
Chin H. Chan
Keyword(s):  
Thermal Properties ◽  
Ethylene Oxide ◽  
Natural Rubber ◽  
Methyl Methacrylate ◽  
Poly Methyl Methacrylate ◽  
Poly Ethylene Oxide ◽  
Poly Ethylene

scholarly journals Analysis of Bio-Based Fatty Esters PCM’s Thermal Properties and Investigation of Trends in Relation to Chemical Structures

2019 ◽  
Vol 9 (2) ◽  
pp. 225 ◽  
Author(s):  
Rebecca Ravotti ◽  
Oliver Fellmann ◽  
Nicolas Lardon ◽  
Ludger Fischer ◽  
Anastasia Stamatiou ◽  
...  
Keyword(s):  
Thermal Properties ◽  
Phase Change ◽  
Energy Demand ◽  
Phase Change Materials ◽  
Arachidic Acid ◽  
Resonance Spectroscopy ◽  
Scanning Calorimetry ◽  
Fatty Esters ◽  
Latent Heat Storage ◽  
Chemical Structures

As global energy demand increases while primary sources and fossil fuels’ availability decrease, research has shifted its focus to thermal energy storage systems as alternative technologies able to cover for the mismatch between demand and supply. Among the different phase change materials available, esters possess particularly favorable properties with reported high enthalpies of fusion, low corrosivity, low toxicity, low supercooling, thermal and chemical stability as well as biodegradability and being derived from renewable feedstock. Despite such advantages, little to no data on the thermal behavior of esters is available due to low commercial availability. This study constitutes a continuation of previous works from the authors on the investigation of fatty esters as novel phase change materials. Here, methyl, pentyl and decyl esters of arachidic acid, and pentyl esters of myristic, palmitic, stearic and behenic acid are synthesized through Fischer esterification with high purities and their properties are studied. The chemical structures and purities are confirmed through Attenuated Total Reflectance Infrared Spectroscopy, Gas Chromatography coupled with Mass Spectroscopy and Nuclear Magnetic Resonance Spectroscopy, while the determination of the thermal properties is performed through Differential Scanning Calorimetry and Thermogravimetric Analysis. In conclusion, some correlations between the melting temperatures and the chemical structures are discovered, and the fatty esters are assessed based on their suitability as phase change materials for latent heat storage applications.

scholarly journals Synthesis and Self-Assembly of Poly(N-Vinylcaprolactam)-b-Poly(ε-Caprolactone) Block Copolymers via the Combination of RAFT/MADIX and Ring-Opening Polymerizations

Polymers ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1252
Author(s):  
Rodolfo M. Moraes ◽  
Layde T. Carvalho ◽  
Gizelda M. Alves ◽  
Simone F. Medeiros ◽  
Elodie Bourgeat-Lami ◽  
...  
Keyword(s):  
Block Copolymers ◽  
Ring Opening ◽  
Chain Transfer ◽  
Fluorescence Probe ◽  
Size Exclusion ◽  
Proton Nuclear Magnetic Resonance ◽  
Solution Temperature ◽  
Copolymer Composition ◽  
Resonance Spectroscopy ◽  
Scanning Calorimetry

Well-defined amphiphilic, biocompatible and partially biodegradable, thermo-responsive poly(N-vinylcaprolactam)-b-poly(ε-caprolactone) (PNVCL-b-PCL) block copolymers were synthesized by combining reversible addition-fragmentation chain transfer (RAFT) and ring-opening polymerizations (ROP). Poly(N-vinylcaprolactam) containing xanthate and hydroxyl end groups (X–PNVCL–OH) was first synthesized by RAFT/macromolecular design by the interchange of xanthates (RAFT/MADIX) polymerization of NVCL mediated by a chain transfer agent containing a hydroxyl function. The xanthate-end group was then removed from PNVCL by a radical-induced process. Finally, the hydroxyl end-capped PNVCL homopolymer was used as a macroinitiator in the ROP of ε-caprolactone (ε-CL) to obtain PNVCL-b-PCL block copolymers. These (co)polymers were characterized by Size Exclusion Chromatography (SEC), Fourier-Transform Infrared spectroscopy (FTIR), Proton Nuclear Magnetic Resonance spectroscopy (1H NMR), UV–vis and Differential Scanning Calorimetry (DSC) measurements. The critical micelle concentration (CMC) of the block copolymers in aqueous solution measured by the fluorescence probe technique decreased with increasing the length of the hydrophobic block. However, dynamic light scattering (DLS) demonstrated that the size of the micelles increased with increasing the proportion of hydrophobic segments. The morphology observed by cryo-TEM demonstrated that the micelles have a pointed-oval-shape. UV–vis and DLS analyses showed that these block copolymers have a temperature-responsive behavior with a lower critical solution temperature (LCST) that could be tuned by varying the block copolymer composition.

Magnetic Properties of Irradiated Nickel Ferrite Thermoplastic Natural Rubber Nanocomposite

2014 ◽  
Vol 879 ◽  
pp. 206-212 ◽  
Author(s):  
Sivanesan Appadu ◽  
Sahrim Hj. Ahmad ◽  
Chantara Thevy Ratnam ◽  
Meor Yahaya Razali ◽  
Moayad Husein Flaifel ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Thermal Properties ◽  
Natural Rubber ◽  
Weight Ratio ◽  
Xrd Analysis ◽  
Degree Of Crystallinity ◽  
Scanning Calorimetry ◽  
Magnetic Microstructure ◽  
Sem Image ◽  
Thermoplastic Natural Rubber

The effect of electron beam (EB) irradiation at different doses on the magnetic, microstructure, morphological and thermal properties of NiFe2O4/Thermoplastic Natural Rubber (TPNR) nanocomposite was investigated. The NiFe2O4/TPNR nanocomposite samples were prepared by using a Haake mixer in weight ratio of 12:88. The TPNR matrix consists of natural rubber (NR), liquid natural rubber (LNR) and high density polyethylene (HDPE) in weight ratio of 20:10:70. The samples were irradiated using a 2 MeV EB machine in doses from 0 - 200 kGy. Magnetic properties studied by using the vibrating sample magnetometer (VSM) at room temperature showed that the values of saturation magnetization (MS), remanence magnetization (MR) and the coercivity (HC) value increased with increasing doses of irradiation. The increase in MSand MRvalues is attributed to the increase in concentration of Fe3+ions at octahedral B-site and decrease of concentration at the tetrahedral A-site in the NiFe2O4cubic structure. X-ray diffraction (XRD) analysis of the samples showed that peak intensities decreased and the width of the peaks increased with increasing doses of irradiation. Scanning electron microscope (SEM) image of the nanocomposite cross section showed the presence of defects which is more visible with increasing doses of irradiation. In the case of thermal properties, differential scanning calorimetry (DSC) analysis showed that the crystallization temperature (Tc) and the degree of crystallinity (Xc) of the nanocomposite samples decreased with increasing doses of irradiation due to crosslinking of polymeric chains which hinders the growth of crystals.

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