• Elastomers and Composites
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• v.25 no.3
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• pp.195-202
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• 1990

Rubber-modified polyurethane resin which was prepolymer type terminated with NCO, was synthesized by reacting isocyanate groups[NCO] and hydroxyl groups[OH]. Polybutadiene rubbers which had OH groups in the side of rubber chains, were charged at ratio $0%{\sim}40%$ of solid component in reactants. For products, physical properties were investigated experimentally. The results abtained in experiment were as follows. 1. Liquid resin and dried film was good solubility and clearity at less than 25%, 20% of rubber without being related to sort. 2. G-1000 showed better properties than R-45HT in solubility, dring time and adhesive strength. 3. Dring time and adhesive strength were considerably influenced by molecular weigh and structure of rubber. 4. In using 25% of mixed rubber(G-1000/R-45HT=50/50), It represented best properties in dring time(10 minute) and adhesive strength($23Kg/cm^2$).

• Elastomers and Composites
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• v.35 no.3
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• pp.215-226
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• 2000

Cure characteristics of carbon black-filled rubber compounds with different rubber composition were studied using a rheometer. The carbon black-filled rubber compounds with single, binary, and ternary rubber compositions of natural rubber (NR), styrene-butadiene rubber (SBR), and butadiene rubber (BR) were used. Delta-torques of the NR/BR- and SBR/BR-based compounds with a high BR content were higher than those of the single rubber-based compounds. For ternary rubber-based compounds, the delta-torques of the compounds were lower when the difference in the rubber content ratios was small than when it was big. Scorch and optimum cure times of the rubber compounds became shorter by increasing the content of NR in the compounds while those became longer by increasing the SBR content. Cure rates of the rubber compounds increased with a decrease of the SBR content in the rubber compounds. Reversion ratios decreased with an increase of the SBR content in the rubber compounds.

• Journal of the Korean Society of Safety
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• v.18 no.4
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• pp.57-63
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• 2003

Thermal degradation of Acrylonitrile butadiene rubber(NBR), which is used for O-ring material as elastomeric sealed diaphragm value in the nuclear power plants, is examined. The thermal degradation is accelerated at 130$^{\circ}C$ by Arrhenius exploit method using the activation energy calculated by thermogravimetric analysis. The weight loss temperature and glass transition temperature are verified for thermally aged NBR. The relationship between dynamic mechanical properties and elongation at break are also investigated. The threshold alue of thermally aged NBR is a ten year in the change of elongation at break.

• Computers and Concrete
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• v.21 no.6
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• pp.705-715
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• 2018

This paper presents an experimentally investigation pertinent to the mechanical properties of rubberized mortar (RM) with styrene-butadiene rubber (SBR). The SBR were used with constant water-to-cement ratio of 0.485 and two different volume proportion of SBR particles were utilized as aggregates. One types of SBR particles with fineness modulus of 4.951 were utilized 0%, 10%, and 20% of aggregate volume. Effectiveness of SBR replacement ratio, curing and aging effect on the compressive strength, flexural strengths as well as load-displacement. Compressive and flexural strength of concrete were investigated at the end of 28-days and 56-days age. Obtained results demonstrated that utilization of SBR reduced the flexural strength of SBR mortar at the earlier curing age while SBR increased. Moreover, mechanical properties of mortar mentioned above were significantly affected by the water cure timing with an increasing proportion of the replacement level of SBR.

• Korea-Australia Rheology Journal
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• v.12 no.2
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• pp.135-141
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• 2000

The linear viscoelastic behavior of acrylonitrile-butadiene-styrene (ABS) polymers with different rubber content has been investigated in the frame of a linear viscoelastic model, which takes into account the inter-connectivity of the dispersed rubber particles. The model developed in our previous work has been shown to properly predict the low frequency plateau for the storage modulus, which is generally observed in polymer blends containing core-shell-type impact modifiers. In the present study, further experiments have been carried out on ABS polymers with different rubber content to verify the validity of our linear viscoelastic model. It has been found that our model describes quite properly the rheological behavior of ABS polymers with different rubber content, especially at low frequencies. The experimental data confirm that our model describes the rheological properties of rubber-modified thermoplastic polymers with strong adhesion at the particle/matrix interface more accurately than the Palierne model.

• Elastomers and Composites
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• v.34 no.4
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• pp.332-340
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• 1999

Hydrogenations of BR and NR performed by a noncatalytic method using p-toluenesulphonylhydrazide were carried out by reactive processing. The experimental procedures for carrying out the reaction were established. Two steps comprising premixing of the rubber with TSH followed by hydrogenation in compression mould were proved to be suitable. The percentages of hydrogenation attained by reactive processing were higher than those of the reaction carried out in solution at the same [TSH]/[C=C] ratio, reaction temperature and time. In-creasing the reaction temperature and reaction time resulted in increases of the percentage of hydrogenation. For BR, the maximum percentage of hydrogenation obtained was 36% at [TSH]/[C=C]=1/1.5. For NR, the highest percentage of hydrogenation was 34% at [TSH]/[C=C]=1/1.5. Cis-trans isomerisation was also observed to occur during hydrogenation of both BR and NR. Thermal stabilities of the hydrogenated BR and NR were shown to improve over those or the unhydrogenated counterparts.

• Elastomers and Composites
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• v.50 no.3
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• pp.196-204
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• 2015

Crosslink density of a rubber vulcanizate determines the chemical and physical properties, while bound rubber is an important factor to estimate reinforcement of a filled rubber compound. Extender oil is added to a raw rubber with very high molecular weight for improving processability of a rubber composite. Influence of extender oil on crosslink density, bound rubber formation, and physical properties of solution styrene-butadiene rubber (SSBR) composites with differing microstructures was investigated. Crosslink densities of non-oil-extended SSBR (NO-SSBR) vulcanizates were higher than those of oil-extended SSBR (OE-SSBR) ones. Bound rubber contents of NO-SSBR compounds were also greater than those of OE-SSBR ones. The experimental results could be explained by interfering of extender oil. The OE-SSBR vulcanizates had low modulus but long elongation at break, whereas the NO-SSBR ones had high modulus but short elongation at break. It was found that the crosslink densities affected the physical properties more than the bound rubber contents. The moduli increased with increase in the crosslink density irrespective of extender oil, while the elongation at break decreased. Each variation of the tensile strengths of NO-SSBR and OE-SSBR vulcanizates with the crosslink density showed a decreasing trend. Tear strength of the OE-SSBR vulcanizate increased with increase in the crosslink density, whereas variation of the tear strength of NO-SSBR vulcanizate with the crosslink density showed a weak decreasing trend.

• Elastomers and Composites
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• v.48 no.1
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• pp.46-54
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• 2013

A new terpolymer, styrene-butadiene-benzyl methacrylate copolymer (BzMA-SBR) was synthesized by emulsion polymerization. After polymerization, XSBR ionomer was prepared by deprotection of benzyl group of BzMA through hydrolysis with NaOH. Carboxyl group contents can be controlled by changing the initial feed contents of BzMA. Structure of BzMA-SBR and XSBR were characterized by FTIR, $^1H$ NMR and DSC.

• Elastomers and Composites
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• v.54 no.4
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• pp.335-344
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• 2019

In this work, styrene butadiene rubber (SBR) and styrene butadiene styrene (SBS) were used to modify asphalt, resulting in SBR- and SBS-modified asphalt, respectively. The two modified asphalts were emulsified with a nonionic emulsifier (Span 60) and cationic emulsifiers (ID, DDA) and their phase stabilization was investigated via particle size, Zeta potential, and flow behavior analysis. With increasing amount of the mixed emulsifier, the particle size decreased, leading to an increase in viscosity. The shear thinning behaviors and Zeta potential values ranging from 35-65 mV were determined and remained considerably stable. In addition, the adhesion strength and compression strength of the SBR-and SBS-modified asphalt emulsion were evaluated via surface free energy examination. The remarkable adhesion and compression strengths were estimated when 5 phr ID and 6 phr DDA were added to the emulsified asphalt modified with SBR and SBS. Therefore ID and DDA, the two cationic surfactants, played significant roles in improving the dispersion and interfacial adhesion strength, resulting in the improved adhesion and compression strength of the emulsified asphalts modified with SBR and SBS.

• Bulletin of the Korean Chemical Society
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• v.22 no.10
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• pp.1145-1148
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• 2001