Tack and Green Strength of NR, SBR and NR/SBR Blends

1981 ◽  
Vol 54 (2) ◽  
pp. 403-414 ◽  
Author(s):  
G. R. Hamed

Abstract 1. A simple NR compound has superior tack compared to an SBR stock because of its greater ability to flow under compressive load and its higher green strength. The difference becomes greater as surface roughness is increased or test rate decreased. Tack differences between the two stocks can be quantitatively explained without assuming differences in the interdiffusion rate of SBR and NR molecules. NR is an “ideal” material for developing high tack. It can be processed to a low viscosity and still maintain high green strength. Furthermore, the mechanism responsible for the high green strength (strain crystallization) is not active in the bond formation step, hence does not interfere with contact and interdiffusion, but rather develops upon stressing. SBR, on the other hand, depends on entanglements, which tend to inhibit flow, to achieve green strength. Thus, if the molecular weight of the SBR is raised to enhance green strength to the level of NR, the stock will flow very poorly. Likewise, if SBR molecular weight is lowered, flow can be improved substantially, but green strength will decrease rapidly. Either of the above conditions result in poor tack. 2. For smooth, shiny surfaces brought together, contact occurs rapidly and nearly completely for both the NR and SBR stocks. This results in a relative tack near unity and hence, in this case, the tack strength is really a measure of stock green strength, i.e., tack is green strength limited. Obviously, when this condition exists, the addition to the stock of plasticizers, tackifiers, oils or other additives to facilitate stock flow (but decrease green strength) will nontheless reduce tack. Here, tack can only be increased by enhancing stock green strength, preferable without hindering flow ability. 3. The relative tack of SBR and SBR-dominated blends with moderately rough surfaces is less than unity and increases with contact pressure. Thus, tack is contact limited. In this instance, relative tack can be improved by decreasing stock viscosity, however, absolute tack will only be increased if good green strength is maintained. This may be the mechanism for the action of commencal tackifiers. 4. The tack of NR/SBR blends passes through a maximum with composition at about 80% NR. This is readily understood by noting that the green strength also reaches a maximum at this composition. For NR/SBR blends containing 60% or more of NR, green strength plays the dominant role in controlling tack. 5. Uncured adhesion of SBR to NR is less than the tack of either pure component. This suggests that interdiffusion is required to obtain high tack.

2013 ◽  
Vol 13 (3) ◽  
Author(s):  
Netty Widyastuti ◽  
Teguh Baruji ◽  
Henky Isnawan ◽  
Priyo Wahyudi ◽  
Donowati Donowati

Beta glucan is a polysaccharide compound, generally not soluble inwater and resistant to acid. Beta glucan is used as an immunomodulator (enhancing the immune system) in mammals is usually a beta-glucan soluble in water, easily absorbed and has a low molecular weight. Several example of beta-glucan such as cellulose (β-1 ,4-glucan), lentinan (β-1 0.6-glucan) and (β-1 ,3-glucan), pleuran (β-1, 6 and β-1 ,3-glucan) are isolated from species of fungi Basidiomycota include mushrooms (Pleurotus ostreatus) and shiitake (Lentinus edodes).The purpose of thisresearch activity is to obtain beta-glucan compound that can be dissolved in water and in alkali derived from fungi Basidiomycota, i.e, Oyster mushrooms (Pleurotus ostreatus) and shiitake (Lentinus edodes). The result of beta-glucan compared to characterize the resulting beta glucan that is molecular structure . The difference of beta glucan extraction is based on the differences in solubility of beta-glucan. Beta glucan could be water soluble and insoluble water.


Author(s):  
Nayara Dantas Coutinho ◽  
Hugo Gontijo Machado ◽  
Valter Henrique Carvalho-Silva ◽  
Wender A. Silva

Recent studies have assigned hydroxide elimination and C=C bond formation step in base-promoted aldol condensation the role of having a strong influence in the overall rate reaction, in contrast to...


2016 ◽  
Vol 139 (1) ◽  
Author(s):  
Scott Bair ◽  
Tsuyoshi Yamaguchi

Measurements are reported for dipentaerythritol hexaisononanoate (DiPEiC9) of pressure–volume–temperature (pVT) response to pressures to 400 MPa and temperatures to 100 °C, and of viscosity at pressures to 700 MPa and temperatures to 90 °C and shear stress to 18 MPa. These data complement the low-shear viscosities published by Harris to pressures to 200 MPa and the compressions by Fandiño et al. to 70 MPa. The improved Yasutomi correlation reproduces all viscosity measurements with accuracy better than the Doolittle free volume and the Bair and Casalini thermodynamic scaling models which require an equation of state (EoS). The interaction parameter for thermodynamic scaling, γ = 3.6, is less than that reported by Harris (γ = 4.2) and the difference is primarily in the choice of EoS. The shear stress at the Newtonian limit, about 6 MPa, is exceptionally large given the high molecular weight of DiPEiC9. The large Newtonian limit is also seen in the oscillatory shear response.


1974 ◽  
Vol 47 (2) ◽  
pp. 342-356 ◽  
Author(s):  
V. A. Grechanovskii ◽  
I. Ya Poddubnyi ◽  
L. S. Ivanova

Abstract By changing the sol-gel ratio and the structure of the gel fraction it is possible to obtain various grades of synthetic cis-poly(isoprene) which show promise for different applications in the tire and mechanical rubber goods industries. The processability of commercial SKI-3 rubber (at a given average molecular weight of sol) depends mainly on the structure of the gel fraction. Thus, for example, inferior processing properties of rubber compounds is associated primarily with the presence of tight gel. The content and structure of the gel fraction also significantly affect plasto-elastic properties of raw rubbers, e.g. a low plasticity of raw rubbers owes to the increased content of gel fraction. The reduced green strength of compounds based on SKI—3 rubber is accounted for by its chemical structure. Conventional methods used to change the properties of rubbers (including the variation in molecular weight, molecular weight distribution, branching degree, and variation in the content and structure of gel fraction) cannot be considered to be adequate to tackle the problem of the green strength of SKI—3 black stocks. The way to solve the problem appears to be the introduction of functional groups into the polymer chain at the stage of synthesis or processing. These functional groups should be active as to the formation of labile rubber—carbon black—rubber and/or rubber—rubber bonds. High purity of microstructure is necessary but not sufficient for obtaining the required level of green strength of compounded SKI—3. The gel fractions of SKI—3 rubber yield vulcanizates with a more dense network than the corresponding sol vulcanizates. The temperature dependence of the tensile strength is controlled by the network density of vulcanizates from high cis-1,4 poly(isoprene).


1983 ◽  
Vol 31 (6) ◽  
pp. 615 ◽  
Author(s):  
B Dell ◽  
JR Bartle ◽  
WH Tacey

The role of root channels in the occupation of deep soil profiles by jarrah (Eucalyptus marginata Sm.) forest in south-western Australia was explored by coring and excavation. In profiles derived from granite, major descending roots are confined to channels that extend vertically from fissures and conduits in the shallow subsurface caprock layer deep in the clay subsoil. The channels are permanent features of the profile and are occupied by successive generations of trees. The channels have a diameter of 1-300 mm, abundance of 3 5 m-2 (all channels) or 1 m-2 (large channels), and occupy 1% of a horizontal surface at 6 m. Each forest tree has potential access to 100-200 channels. Large roots, fine roots with root hairs, and decaying root remains occur in the channels. Only fine roots (less than Imm diam.) penetrate the clay matrix and occupy the entire profile down to basement at depths of up to 40 m. In profiles derived from dolerite, occupation of the deep clay by large and fine roots is diffuse and root channels are absent. The dissimilar mode of root occupation of the two profile types may be explained by the difference in bulk density. In providing avenues for access by large roots as well as preferential wetting, the root channels may play a dominant role in the water and salt balance of jarrah forests on the granitic profile.


2008 ◽  
Vol 149 (1) ◽  
pp. 412-423 ◽  
Author(s):  
Alessio Lombardi ◽  
Alessandra Barbante ◽  
Pietro Della Cristina ◽  
Daniele Rosiello ◽  
Chiara Lara Castellazzi ◽  
...  

Author(s):  
Kazuya Tada ◽  
Daiya Fujimoto

Abstract Electrophoretic deposition provides material-efficient film formation on large area electrodes. In this study, it has been found that there is a significant difference in the colloidal particle formation process between a thiophene-based copolymer poly(3-octylthiophene- 2,5-diyl-co-3-decyloxythiophene-2,5-diyl) (POT-co-DOT) and C60 in preparation of suspension for electrophoretic deposition by reprecipitation method. This difference is attributed to the difference between low molecular weight materials with specific molecular weight and polymers with molecular weight distribution. The composition of POT-co-DOT:C60 composite film by electrophoretic deposition has also been estimated.


1979 ◽  
Vol 34 (1-2) ◽  
pp. 20-26 ◽  
Author(s):  
Ingrid Pilz ◽  
Karin Goral ◽  
Friedrich v. d. Haar

Abstract The quaternary structure of the phenylalanyl-tRNA synthetase and its complex with tRNAPhe was studied in dilute solutions by small angle X-ray scattering. For the free synthetase the radius of gyration was determined as 5.5 nm, the volume 523 nm3, the maximum diameter 17.5 nm and the molecular weight as 260 000 using an isopotential specific volume of 0.735. The overall shape could be best approximated by a flat cylinder with dimensions 18.2 nm X 11.5 nm X 4 nm ; the loose structure was approximated by building up the cylinder by spheres (diameter 4.2 nm).The corresponding parameters of the enzyme tRNA complex were the following: radius of gyration 5.9 nm, volume 543 nm 3, maximum diameter 21 nm and molecular weight 290 000. These parameters suggest an 1:1 complex, whereby it must be assumed that the tRNA molecule is attached in the extension of the longer axis. From the difference in the distance distribution functions of the free enzyme and the complex it is evident that we have to assume a change of conformation (contraction) of the enzyme upon the binding of the specific tRNA.


2020 ◽  
Vol 10 (10) ◽  
pp. 3619
Author(s):  
Marina Simunovic Anicic ◽  
Cecilia Goracci ◽  
Jelena Juloski ◽  
Ivana Miletic ◽  
Senka Mestrovic

Prior research reveal that low-viscosity resin is able to significantly penetrate initial caries lesions, which leads to their stabilization. The objective of the present report is to assess the shear bond strength (SBS) of orthodontic brackets bonded with different adhesives to demineralized enamel treated with a low-viscosity resin infiltrant. It also aims to compare the achieved bond strengths to those achieved in relation to sound enamel (SE). A total of 48 newly extracted third molars were collected, distributed in four groups (n=12), covered with a nail varnish, with 4 x 4 mm of uncoated area, immersed in Buskes demineralizing solution (14 days, 37 °C) or remained untreated. Group I: SE + Transbond XT; Group II: demineralized enamel (DE) + ICON + Transbond XT; Group III: DE + ICON + Scotchbond Universal; Group IV: DE + ICON + Assure PLUS. SBS was quantified in megapascals (MPa) and statistically analyzed (ANOVA, p ≤ 0.05). The mode of failure was assessed microscopically (10 x magnification). The highest SBS detected was in Group IV, and the difference was statistically significant (F = 14.37; p = 0.000). Treatment with a resin infiltrant on DE does not impair the shear bond strength when compared to SE, although it does produce a significantly higher strength when combined with Assure PLUS.


2015 ◽  
Vol 4 (2) ◽  
pp. 319-329 ◽  
Author(s):  
Tripti Mishra ◽  
RK Srivastava

The current study aims at the selection of an appropriate draw solute for forward osmosis process. Separation and recovery of the draw solute are the major criteria for the selection of draw solute for forward osmosis process. Therefore in this investigation six inorganic fertilizers draws solute were selected. The selections of inorganic fertilizers as draw solute eliminate the need of removal and recovery of draw solute from the final product. The final product water of forward osmosis process has direct application in agricultural as nutrient rich water for irrigation. These inorganic fertilizers were tested based on their water extraction (water flux) capacity. This experimental water flux was compared with the observed water flux. It was noted that the observed water flux is much higher than the attained experimental water flux. The difference of these two fluxes was used to calculate the performance ratio of each selected fertilizer. Highest performance ratio was shown by low molecular weight compound ammonium nitrate (22.73) and potassium chloride (21.03) at 1 M concentration, whereas diammonium phosphate (DAP) which has highest molecular weight among all the selected fertilizer show the lowest performance ratio (10.02) at 2 M concentration. DOI: http://dx.doi.org/10.3126/ije.v4i2.12660 International Journal of Environment Vol.4(2) 2015: 319-329


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