scholarly journals Effects of Molecular Weight of Functionalized Liquid Butadiene Rubber as a Processing Aid on the Properties of SSBR/Silica Compounds

Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 850
Author(s):  
Donghyuk Kim ◽  
Byungkyu Ahn ◽  
Kihyun Kim ◽  
JongYeop Lee ◽  
Il Jin Kim ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Anionic Polymerization ◽  
High Performance ◽  
Crosslink Density ◽  
Functional Group ◽  
Vital Role ◽  
Butadiene Rubber ◽  
Molecular Weights ◽  
Mooney Viscosity ◽  
Silica Dispersion

Liquid butadiene rubber (LqBR) which used as a processing aid play a vital role in the manufacturing of high-performance tire tread compounds. However, the studies on the effect of molecular weight, microstructure, and functionalization of LqBR on the properties of compounds are still insufficient. In this study, non-functionalized and center-functionalized liquid butadiene rubbers (N-LqBR and C-LqBR modified with ethoxysilyl group, respectively) were synthesized with low vinyl content and different molecular weights using anionic polymerization. In addition, LqBR was added to the silica-filled SSBR compounds as an alternative to treated distillate aromatic extract (TDAE) oil, and the effect of molecular weight and functionalization on the properties of the silica-filled SSBR compound was examined. C-LqBR showed a low Payne effect and Mooney viscosity because of improved silica dispersion due to the ethoxysilyl functional group. Furthermore, C-LqBR showed an increased crosslink density, improved mechanical properties, and reduced organic matter extraction compared to the N-LqBR compound. LqBR reduced the glass transition temperature (Tg) of the compound significantly, thereby improving snow traction and abrasion resistance compared to TDAE oil. Furthermore, the energy loss characteristics revealed that the hysteresis loss attributable to the free chain ends of LqBR was dominant.

Viscosity and Molecular Weight of Masticated Styrene-Butadiene Rubber

1965 ◽  
Vol 38 (4) ◽  
pp. 961-966 ◽  
Author(s):  
S. K. Bhatnagar ◽  
S. Banerjee
Keyword(s):  
Molecular Weight ◽  
Intrinsic Viscosity ◽  
Crosslink Density ◽  
Empirical Relation ◽  
Styrene Butadiene Rubber ◽  
Butadiene Rubber ◽  
Mooney Viscosity ◽  
The Times ◽  
Styrene Butadiene

Abstract Changes in the value of [η], [ηm], K′, (M) and μ of SBR masticated in the cold at 25.0 ± 5.0° C in presence of oxygen with the times of mastication are reported. An empirical relation has been developed between the intrinsic viscosity [η] and Mooney viscosity [ηm] which permits molecular weight of the rubber to be determined directly from Mooney viscosity. The value of g which appears in the Flory equation connecting true crosslink density with the physically determined one has been calculated for unfilled SBR.

Comparison of exopolysaccharides from mucoid and nonmucoid strains of Clavibacter michiganensis subspecies sepedonicus

1993 ◽  
Vol 39 (3) ◽  
pp. 291-296 ◽  
Author(s):  
Paul J. Henningson ◽  
Neil C. Gudmestad
Keyword(s):  
Molecular Weight ◽  
High Performance ◽  
Size Exclusion ◽  
Enzyme Linked Immunosorbent Assay ◽  
Low Molecular Weight ◽  
Neutral Sugar ◽  
Clavibacter Michiganensis ◽  
Serological Reaction ◽  
Molecular Weights ◽  
Exclusion Chromatography

The exopolysaccharides produced by six strains of Clavibacter michiganensis ssp. sepedonicus were isolated and purified by liquid chromatography. Neutral sugar composition and molecular weights were determined for each polysaccharide fraction, using gas chromatography and high-performance size-exclusion chromatography. The serological reaction of each fraction was tested using enzyme-linked immunosorbent assay. Exopolysaccharide from nonmucoid strains contained only low molecular weight polysaccharides (1.5 × 103 to 1.1 × 104). Exopolysaccharide from mucoid and intermediate strains could be separated into low (4.0 × 103 to 1.1 × 104) molecular weight and high (5.0 × 105 to 1.6 × 106) molecular weight fractions. High molecular weight polysaccharides were composed almost exclusively of galactose, glucose, and fucose. The ratios of these sugars were highly variable among strains. Low molecular weight polysaccharides were primarily composed of galactose with significant and varying amounts of glucose, rhamnose, mannose, and ribose. All polysaccharide fractions except one, produced by a nonmucoid strain, reacted in the immunoassay test.Key words: exopolysaccharide, polysaccharide, Clavibacter, michiganensis, sepedonicus.

Particulate glycogen of mammalian liver: specificity in binding phosphorylase and glycogen synthase

1992 ◽  
Vol 70 (7) ◽  
pp. 523-527 ◽  
Author(s):  
Alexander Vardanis
Keyword(s):  
Molecular Weight ◽  
High Performance ◽  
Glycogen Phosphorylase ◽  
Hydrophobic Interactions ◽  
Glycogen Synthase ◽  
Early Period ◽  
Glycogen Particle ◽  
Molecular Weights ◽  
Glycogen Deposition ◽  
A Minor

The glycogen particle – glycogen metabolizing enzyme complex was investigated to gain some understanding of its physiological significance. Fractionations of populations of particles from mouse liver were carried out utilising open column and high performance liquid chromatography, and based either on the molecular weight of the particles or the hydrophobic interactions of the glycogen-associated proteins. The activities of glycogen phosphorylase and glycogen synthase were measured in these fractions. Fractionations were of tissue in different stages of glycogen deposition or mobilization. In animals fed ad libitum, glycogen synthase was associated with the whole spectrum of molecular weights, while the glycogen phosphorylase distribution was skewed in favour of the lower molecular weight species. Under conditions of glycogen mobilization, the phosphorylase distribution changed to include all molecular weights. The hydrophobic interaction separations demonstrated that glycogen synthase binds to a specific subpopulation of particles that is a minor proportion of the total. In general, there was a direct relationship of the total amount of phosphorylase and synthase bound during periods of mobilization and deposition, respectively. Two notable exceptions were the large amounts of glucose-6-P dependent synthase present during the early period of glycogen mobilization and the high amounts of active phosphorylase appearing shortly after food withdrawal, in spite of interim glycogen deposition from presumably already ingested food.Key words: glycogen particle, glycogenolysis, glycogenesis, glycogen phosphorylase, glycogen synthase.

Influence of TMTD on Cross-Linking Degradation of the Waste Tire Rubber

2017 ◽  
Vol 732 ◽  
pp. 43-49
Author(s):  
Guo Liang Tao ◽  
Yan Ping Xia ◽  
Hao Ran Gen ◽  
Jian Yang ◽  
Wei Wang
Keyword(s):  
Molecular Weight ◽  
Crosslink Density ◽  
Cross Linking ◽  
Tire Rubber ◽  
Gel Content ◽  
Waste Tire ◽  
Waste Tire Rubber ◽  
Mooney Viscosity ◽  
Recycled Rubber ◽  
Mechanical Shearing

The paper studied the thermal mechanical shearing of waste tire rubber (WTR) by tetra methyl thiuram disulfide (TMTD), a reclaiming agent. The results showed that the mooney viscosity, gel content and crosslink density of the WTR decreased with the increasing TMTD amount. The mechanical properties of recycled rubber were best in the amount of 1% TMTD, which could reach 14MPa and 368%, respectively. The molecular weight of WTR was analyzed by gel permeation chromatorgraphy (GPC). The molecular weight of rubber dropped more faster when the content of TMTD from 0.5% to 1%. The plausible reaction mechanism of TMTD on the process of cross-linking degradation was predicted based on the changes of the mooney viscosity, gel content, crosslink density and the relation between the molecular weight and the Raman spectroscopy of the sol fraction.

scholarly journals Preparation of High Molecular Weight Poly(urethane-urea)s Bearing Deactivated Diamines

Polymers ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 1914
Author(s):  
Alejandra Rubio Hernández-Sampelayo ◽  
Rodrigo Navarro ◽  
Ángel Marcos-Fernández
Keyword(s):  
Molecular Weight ◽  
Experimental Work ◽  
High Performance ◽  
Polymerization Reaction ◽  
Quantum Mechanical ◽  
Synthetic Approach ◽  
Molecular Weights ◽  
Mechanical Methods ◽  
Electronic Parameters ◽  
High Molecular Weight Poly

The synthesis of poly(urethane-urea) (PUUs) bearing deactivated diamines within the backbone polymer chain is presented. Several deactivated diamines present interesting properties for several applications in the biomaterial field due to their attractive biocompatibility. Through an activation with Chloro-(trimethyl)silane (Cl-TMS) during the polymerization reaction, the reactivity of these diamines against diisocyanates was triggered, leading to PUUs with high performance. Indeed, through this activation protocol, the obtained molecular weights and mechanical features increased considerably respect to PUUs prepared following the standard conditions. In addition, to demonstrate the feasibility and versatility of this synthetic approach, diisocyanate with different reactivity were also addressed. The experimental work is supported by calculations of the electronic parameters of diisocyanate and diamines, using quantum mechanical methods.

INTRODUCING BIOBASED NONPOLAR BOTTLEBRUSH β-MYRCENE SEGMENTS TO IMPROVE SILICA DISPERSION FOR SUSTAINABLE SSBR/SILICA NANOCOPOSITES

2021 ◽  
Author(s):  
Jingwei Zhang ◽  
Jianmin Lu ◽  
Dongfang Wang ◽  
Bingyong Han
Keyword(s):  
Electron Microscopy ◽  
High Performance ◽  
Rolling Resistance ◽  
Styrene Butadiene Rubber ◽  
Butadiene Rubber ◽  
Double Bonds ◽  
Silica Nanocomposites ◽  
Green Solution ◽  
Silica Dispersion ◽  
Styrene Butadiene

ABSTRACT To overcome the problem of fossil fuel depletion and associated environmental issues arising from the use of tire tread elastomers, a convenient, environmentally friendly, and highly efficient strategy was developed to prepare high-performance green solution polymerized styrene–butadiene rubber (SSBR)/silica nanocomposites by improving silica dispersion in the nonpolar polymer matrix via the introduction of a biobased nonpolar bottlebrush segment with two double bonds. Various elastomers containing biobased nonpolar bottlebrush β-myrcene segments were synthesized using an industrially robust anionic polymerization method. Results of robotic process automation, small-angle X-ray scattering, scanning electron microscopy, and transmission electron microscopy revealed that rubber with myrcene could significantly improve silica dispersibility and inhibit the strong filler–filler interactions, which are due to the formation of hydrogen bonding between the double bonds in the myrcene block and silanol groups on the silica surface and possibly to the spreading or infiltrating of myrcene bottlebrush segments onto silica. Furthermore, for the modified rubber, rolling resistance decreased by 41.7%, tear strength increased by 20.78%, and tensile strength increased by 77.8% with the elongation at break remained practically unchanged as compared with the unmodified silica/SSBR composite. On the basis of aforementioned assessment, we believe that silica-reinforced β-myrcene–based styrene–butadiene integrated rubber is a versatile and promising candidate for future tire tread elastomers.

scholarly journals Glycidyl Methacrylate-Emulsion Styrene Butadiene Rubber (GMA-ESBR)/Silica Wet Masterbatch Compound

Polymers ◽  
2019 ◽  
Vol 11 (6) ◽  
pp. 1000 ◽  
Author(s):  
Hyunsung Mun ◽  
Kiwon Hwang ◽  
Eunho Yu ◽  
Woong Kim ◽  
Wonho Kim
Keyword(s):  
Molecular Weight ◽  
Glycidyl Methacrylate ◽  
Functional Group ◽  
Rolling Resistance ◽  
Styrene Butadiene Rubber ◽  
Butadiene Rubber ◽  
Manufacturing Method ◽  
Tire Industry ◽  
Styrene Butadiene ◽  
Resistance Performance

In the tire industry, solution styrene butadiene rubber (SSBR), which can introduce a functional group with good reactivity to silica at chain ends, is used to increase rolling resistance performance by considering fuel economy. However, this is not environmentally friendly because SSBR uses an organic solvent for polymerization, and it is difficult to increase its molecular weight. Functionalized emulsion SBR (ESBR) can solve the problems of SSBR. The molecular weight of ESBR molecules can be easily increased in an eco-friendly solvent, i.e., water. A functionalized ESBR introduces a functional group with good reactivity to silica by introducing a third monomer during polymerization. In this field, glycidyl methacrylate (GMA) has been reported to show the best properties as a third monomer. However, for GMA-ESBR, the viscosity is high and processability is disadvantageous. Therefore, we polymerized GMA-ESBR and manufactured silica compounds to clarify the causes of these problems. In addition, wet masterbatch (WMB) technology, which is a new compound manufacturing method, was applied to manufacture the silica compound, and the physical properties are compared with those of a dry masterbatch. The results clarified the problem of GMA-ESBR, which could be solved by using WMB technology.

Dynamic Mechanical Properties of Cross-Linked Rubbers. II. Effects of Crosslink Spacing and Initial Molecular Weight in Polybutadiene

1966 ◽  
Vol 39 (4) ◽  
pp. 905-914
Author(s):  
Etsuji Maekawa ◽  
Ralph G. Mancke ◽  
John D. Ferry
Keyword(s):  
Molecular Weight ◽  
Crosslink Density ◽  
Low Frequency ◽  
Dynamic Mechanical Properties ◽  
Cross Linking ◽  
Loss Mechanism ◽  
Low Frequencies ◽  
Molecular Weights ◽  
Monomeric Friction Coefficient ◽  
Lower Frequencies

Abstract The complex shear compliances of eight samples of polybutadiene crosslinked by cumyl peroxide and four samples crosslinked by sulfur have been measured over a frequency range from 0.2 to 2 cps at temperatures from − 6 to 45° C by a torsion pendulum. On four of the samples, measurements were extended by the Fitzgerald transducer from 45 to 600 cps at temperatures from − 71 to 55°. The vulcanizates had been prepared from polymers of two different molecular weights (180,000 and 510,000) with sharp molecular weight distribution; the physical crosslink density ranged from 0.57 to 2.68×10−4 mole/cm3, and the chemical crosslink density calculated following Kraus ranged from 0.22 to 1.49×10−4 mole/cm3. The mechanical data were all reduced to T0=298° K by shift factors calculated from the equation log aT=−3.64(T−T0)/(186.5+T−T0). In the transition zone of frequencies, the viscoelastic functions of the cumyl peroxide vulcanizates were closely similar, except for a shift toward lower frequencies with increasing crosslinking, corresponding to a small but unexpected increase in the monomeric friction coefficient. Cross-linking by sulfur caused a somewhat larger shift toward lower frequencies at a comparable crosslink density. In the rubbery zone, the sample with least cross-linking exhibited a substantial secondary loss mechanism at very low frequencies. The low-frequency losses are evident in all the samples, but their magnitude falls rapidly with increasing crosslink density as previously found for natural rubber. It also falls somewhat with increasing initial molecular weight, indicating a contribution from network strands with loose ends. The possible relation of the low-frequency losses to trapped entanglements is discussed.

Effect of Molecular Weight on Dynamic Mechanical Properties of SKD cis-1,4-Butadiene Rubber

1967 ◽  
Vol 40 (2) ◽  
pp. 517-521
Author(s):  
A. I. Marei ◽  
E. A. Sidorovich
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Average Molecular Weight ◽  
Dynamic Mechanical Properties ◽  
Considerable Effect ◽  
Butadiene Rubber ◽  
Dynamic Mechanical ◽  
Temperature Range ◽  
Molecular Weights ◽  
Dynamic Mechanical Behavior

Abstract In the high-elastic temperature range the molecular weight has a considerable effect on the dynamic mechanical properties of linear (uncrosslinked) SKD cis-1, 4-butadiene rubber. In this temperature range an unequivocal correlation exists between the rebound resilience at a given temperature and the viscosity average molecular weight, and the determination of the resilience can therefore be recommended as a rapid method of finding the molecular weight of SKD. A similarity is found in the dynamic mechanical behavior of rubbers of different molecular weights in the high-elastic temperature range. In the low-temperature range an increase in the molecular weight of crystalline polymers of SKD is accompanied by an impairment of their elastic properties.

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