Mixing of Carbon Black with Rubber. VI. Analysis of NR/SBR Blends

1988 ◽  
Vol 61 (4) ◽  
pp. 609-618 ◽  
Author(s):  
George R. Cotten ◽  
Lawrence J. Murphy
Keyword(s):  
Molecular Weight ◽  
Carbon Black ◽  
High Molecular Weight ◽  
Surface Area ◽  
Bound Rubber ◽  
Very High

Abstract The distribution of carbon black in NR/SBR blends was determined through the analysis of bound rubber. The NR/SBR blends were found to be very different from the previously studied SBR/BR compounds: these differences were assigned to mutual insolubility of the two polymers and a very high molecular weight of NR. In NR/SBR blends, it was found that changes in molecular weight of the polymer has no effect on the carbon black distribution in the blend. While the “activity” of carbon black did not affect the distribution, the loading of the black in NR decreased linearly with increasing surface area of the black. Approximately 35% of normal tread blacks (surface area 80–100 m2/g) was found in the NR phase. However, the bond between NR and carbon black is quite weak, and black continues to migrate into the SBR phase on prolonged mixing or during blending of NR and SBR masterbatches.

Molecular Weight Effects in Adsorption of Rubbers on Carbon Black

1968 ◽  
Vol 41 (5) ◽  
pp. 1256-1270 ◽  
Author(s):  
Gerard Kraus ◽  
J. T. Gruver
Keyword(s):  
Molecular Weight ◽  
Carbon Black ◽  
Large Particle ◽  
Molecular Weights ◽  
Molecular Weight Dependence ◽  
Bound Rubber ◽  
Sieve Effect ◽  
High Structure ◽  
Very High ◽  
Poor Solvent

Abstract The molecular weight dependence of the adsorption of polybutadiene on carbon black from a poor solvent, n-heptane, and bulk, i.e., the phenomenon of “bound rubber”, was investigated. For narrow distribution polymers the adsorption is proportional to Mn, where n = 0.14 for adsorption from n-heptane solution; n = 0.5 for adsorption from bulk. Anomalously low solution adsorption was observed for polymers of very high molecular weight (> 500,000). This is ascribed to a sieve effect by aggregates of carbon black particles which cannot be penetrated by the large molecular coils. In high structure blacks, which pack more loosely, and in large particle blacks, which form larger interstices between particles, onset of anomalous adsorption is shifted toward higher molecular weights.

Formation of Bound Rubber of GR-S Type Polymers with Carbon Blacks

1952 ◽  
Vol 25 (3) ◽  
pp. 500-516 ◽  
Author(s):  
June Duke ◽  
W. K. Taft ◽  
I. M. Kolthoff
Keyword(s):  
Molecular Weight ◽  
Carbon Black ◽  
High Molecular Weight ◽  
Lower Molecular Weight ◽  
Carbon Blacks ◽  
Bound Rubber ◽  
Temperature Levels ◽  
Black Other ◽  
Lower Carbon

Abstract The bound rubber-black complex formed by milling various GR-S polymers and carbon blacks at several temperature levels was studied. The amount of bound polymer increased with greater loadings of black, but per unit of carbon black, it decreased at the higher black loadings. The temperature of mixing likewise has a large effect—at lower carbon black loadings, higher temperatures increase the amount of binding; the effect ia minimized as the loading is increased until at high loadings (100 to 125 parts of black per 100 parts of rubber) this effect is eliminated. By fractionation of the sol portion, it has been shown that polymer of progressively lower molecular weight is bound as the black loading is increased. Polymer of high molecular weight does not replace bound polymer of lower molecular weight; the polymer of higher molecular weight is preferentially bound during mill mixing. Although more polymer appears to be bound as the conversion is increased from 50 to 72 per cent at a loading of 50 parts of black, other factors besides conversion may be determinative. No differences in relationship were found for polymers made at 122° or 41° F.

Sorption of GR-S Type of Polymer on Carbon Black. III. Sorption by Commercial Blacks

1953 ◽  
Vol 26 (1) ◽  
pp. 102-114 ◽  
Author(s):  
I. M. Kolthoff ◽  
R. G. Gutmacher
Keyword(s):  
Molecular Weight ◽  
Carbon Black ◽  
Intrinsic Viscosity ◽  
Benzene Solution ◽  
Weight Fraction ◽  
High Molecular Weight Fraction ◽  
Molecular Weights ◽  
Bound Rubber ◽  
Flow Through ◽  
Peculiar Behavior

Abstract The sorption capacities toward GR-S five commercial carbon blacks are in decreasing order: Spheron-6, Vulcan-1, Philblack-0, Sterling-105, Philblack-A. Apparently, the sorption is not related to surface area. The sorption on Vulcan-1 of GR-S from its solutions in seven different solvents or mixtures of solvents increases with decreasing solvent power for the rubber. The sorption curves of two “cold rubbers,” polymerized at −10 and +5° respectively, showed little difference from that of 50° GR-S. Previous heating of carbon black in nitrogen at 500 or 1100° increased the sorption by about 20 per cent over unheated carbon. Air-heating of carbon black at 425° did not cause a difference in the sorption from benzene solution, but produced an increase in the sorption of rubber from n-heptane solution. In the range 75% butadiene-25% styrene to 5% butadiene-95% styrene, there is practically no effect of the degree of unsaturation on the sorption. Polystyrene of high intrinsic viscosity exhibits a peculiar behavior with furnace blacks. Vulcan-1 sorbed microgel as well as the sol fraction from n-heptane solutions of GR-S containing microgel (conversion 74.7 and 81.5 per cent). There was no appreciable difference in the amount of sorption of rubber fractions having average molecular weights varying from 433,000 to 85,000. There is little change in the amount sorbed after two hours of shaking, but the intrinsic viscosity of the residual rubber decreases with time. The low molecular-weight rubber is sorbed more rapidly, but is slowly replaced by the more tightly sorbed high molecular weight fraction. Partial fractionation of a rubber sample can be achieved by allowing the rubber solution to flow through a column of weakly sorbing carbon black. A large portion of the sorbed rubber can be recovered from the column by washing it with a good solvent such as xylene. Bound rubber is produced by intimate mixing of equal parts of carbon black and rubber swollen in chloroform, when the mixture is dried in vacuum at 80° or at room temperature. Milling is not essential to get bound rubber.

scholarly journals The multiple complexes formed by the interaction of platelet factor 4 with heparin

1980 ◽  
Vol 191 (3) ◽  
pp. 769-776 ◽  
Author(s):  
P E Bock ◽  
M Luscombe ◽  
S E Marshall ◽  
D S Pepper ◽  
J J Holbrook
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Chain Length ◽  
Salt Concentration ◽  
Human Platelet ◽  
Platelet Factor 4 ◽  
High Protein ◽  
Platelet Factor ◽  
The Stability ◽  
Very High

The anisotropy of the fluorescence of dansyl (5-dimethylaminonaphthalene-1- sulphonyl) groups covalently attached to human platelet factor 4 was used to detect the macromolecular compounds formed when the factor was mixed with heparin. At low heparin/protein ratios a very-high-molecular-weight compound (1) was formed that dissociated to give a smaller compound (2) when excess heparin was added. 2. A large complex was also detected as a precipitate that formed at high protein concentrations in chloride buffer. It contained 15.7% (w/w) polysaccharide, equivalent to four or five heparin tetrasaccharide units per protein tetramer. In this complex, more than one molecule of protein binds to each heparin molecule of molecular weight greater than about 6 × 10(3).3. The stability of these complexes varied with pH, salt concentration and the chain length of the heparin. The limit complexes found in excess of the larger heparins consisted of only one heparin molecule per protein tetramer, and the failure to observe complexes with four heparin molecules/protein tetramer is discussed.

Effect of Modified Carbon Black on the Processing of NR- and SBR-based Compounds

2009 ◽  
Vol 25 (3) ◽  
pp. 165-186
Author(s):  
Abhijit Adhikary ◽  
Pranab Kumar Sengupta ◽  
Rabindra Mukhopadhyay
Keyword(s):  
Fatty Acid ◽  
Carbon Black ◽  
Surface Area ◽  
Simple Technique ◽  
Acid Moiety ◽  
Polymer Filler ◽  
Lower Viscosity ◽  
Bound Rubber ◽  
Strain Sweep ◽  
Long Chain

A simple technique adopted in the laboratory is able to attach flexible, long-chain, aliphatic, fatty acid moiety on the surface of reinforcing carbon black N330. Modified blacks show less bound rubber by comparison with the control, but their better dispersibility effectively outweighs any reduction in polymer–filler interaction resulting from the smaller available surface area. When subjected to strain sweep, compounds containing modified blacks show a slower reagglomeration rate of filler aggregates compared with the control. The lower viscosity of compounds containing modified blacks indicates improved processability.

Expanding the morphology library of block copolymer self-assemblies with clews of tubules

2017 ◽  
Vol 53 (36) ◽  
pp. 5005-5008 ◽  
Author(s):  
Xiao-Li Sun ◽  
Dong-Ming Liu ◽  
Pan Wang ◽  
Jia-Lin Tan ◽  
Kang-Kang Li ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Block Copolymer ◽  
High Molecular Weight ◽  
Self Assembly ◽  
High Asymmetry ◽  
Very High

Clews of tubules are reported via block copolymer self-assembly of P4VP-b-PS with both high asymmetry and very high molecular weight.

scholarly journals Drag-Reducing Effect in Solutions of Very High Molecular Weight Polystyrene by the Rolling Ball Method

1988 ◽  
Vol 20 (2) ◽  
pp. 169-173 ◽  
Author(s):  
Kunio Nakamura ◽  
Shinichi Odajima ◽  
Kazuya Kizawa ◽  
Tsurutaro Nakagawa
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Rolling Ball ◽  
Very High
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