Natural rubber measurement

Fig. 16. Crystallisation of natural rubber measured by the volume decrease.

Fig. 1. Temperature dependence of the spin-lattice relaxation time (Tj), the rotating frame relaxation time (T,, ), and the spin-spin relaxation time (T ) for natural rubber. Measured at a radio frequency of 30 MHz and amplitude of 10 gauss (ref 9)...

Fig. 15. Dependence of Tj on temperature and pressure in natural rubber, measured at...

Figure 11.16. Efficiency of mastication of rubber at different temperatures. Molecular weights (M) measured after 30-minute mastication of 200 g natural rubber in a size B laboratory Banbury...

In the earlier art, there was some consideration that partial incompatibility of the tackifier resin with the rubber was responsible for the appearance of tack, but this no longer is seriously held in light of continuing studies by many investigators. Aubrey [38] has addressed this in his review of the mechanism of tackification and the viscoelastic nature of pressure sensitive adhesives. Chu [39] uses the extent of modulus depression with added tackifier as a measure of compatibility. Thus in a plot of modulus vs. tackifier concentration, the resin that produces the deepest minimum is the most compatible. On this basis, Chu rates the following resins in order of compatibility for natural rubber rosin ester > C-5 resin > a-pinene resin > p-pinene resin > aromatic resin. 

Tackifying resins enhance the adhesion of non-polar elastomers by improving wettability, increasing polarity and altering the viscoelastic properties. Dahlquist [31 ] established the first evidence of the modification of the viscoelastic properties of an elastomer by adding resins, and demonstrated that the performance of pressure-sensitive adhesives was related to the creep compliance. Later, Aubrey and Sherriff [32] demonstrated that a relationship between peel strength and viscoelasticity in natural rubber-low molecular resins blends existed. Class and Chu [33] used the dynamic mechanical measurements to demonstrate that compatible resins with an elastomer produced a decrease in the elastic modulus at room temperature and an increase in the tan <5 peak (which indicated the glass transition temperature of the resin-elastomer blend). Resins which are incompatible with an elastomer caused an increase in the elastic modulus at room temperature and showed two distinct maxima in the tan <5 curve. 

The specimen was prepared by the following method. After mixing HAF carbon black (50 phr) with natural rubber (NR) in a laboratory mixer, carbon gel was extracted from unvulcanized mixture as an insoluble material for toluene for 48 h at room temperamre and dried in a vacuum oven for 24 h at 70°C. We made the specimen as a thin sheet of the carbon gel (including carbon black) by pressing the extracted carbon gel at 90°C. The cured specimen was given by adding sulfur (1.5 phr) to the unvulcanized mixture and vulcanized for 30 min at 145°C. The dynamic viscoelastic measurement was performed with Rheometer under the condition of 0.1% strain and 15 Hz over temperatures. 

FIGURE 26.74 Abrasion of a natural rubber (NR) and a styrene-butadiene rubber (SBR) tread compound as function of tbe tire surface temperature brought about by ambient temperature changes at a constant slip angle measured with the MRPRA test trailer. 

Garda BE, Barber D, Salcedo G, Rihs HP, Raulf-Heimsoth M Basophil activation test and specific IgE measurements using a panel of recombinant natural rubber latex allergen to determine the latex allergen sensitization profile in children. Pediatr 52 Allergy Immunol 2006 17 148-156. 

This discussion of the structures of diene polymers would be incomplete without reference to the important contributions which have accrued from applications of the ozone degradation method. An important feature of the structure which lies beyond the province of spectral measurements, namely, the orientation of successive units in the chain, is amenable to elucidation by identification of the products of ozone cleavage. The early experiments of Harries on the determination of the structures of natural rubber, gutta-percha, and synthetic diene polymers through the use of this method are classics in polymer structure determination. On hydrolysis of the ozonide of natural rubber, perferably in the presence of hydrogen peroxide, carbon atoms which were doubly bonded prior to formation of the ozonide... 

These conclusions have been confirmed by Wood and Roth, who carried out measurements at both constant lengths and at constant elongations using natural rubber vulcanized with sulfur and an accelerator. Their results at constant elongation, to be considered later in connection with the thermodynamics of rubber elasticity at higher elongations, are summarized in Fig. 89. 

Gee ° has applied this method to the determination of the interaction parameters xi for natural rubber in various solvents. Several rubber vulcanizates were used. The effective value of VelV for each was determined by measuring its extension under a fixed load when swollen in petroleum ether. Samples were then swollen to equilibrium in other solvents, and xi was calculated from the swelling ratio in each. The mean values of xi for the several vulcanizates in each solvent are presented in Table XXXVI, where they are compared with the xi s calculated (Eq. XII-30) from vapor pressure measurements on solutions of unvulcanized rubber in some of the same solvents. The agreement is by no means spectacular, though perhaps no worse than the experimental error in the vapor pressure method. 

Time-crosslink density superposition. Work of Plazek (6) and Chasset and Thirion (3, 4) on cured rubbers suggests that there is one universal relaxation function in the terminal region, independent of the crosslink density. Their results indicate that the molar mass between crosslinks might be considered as a reducing variable. However, these findings were obtained from compliance measurements on natural rubber vulcanizates,... 

A unit in the measurement of microscopic particles. It is one-millionth of a metre or one-thousandth of a millimetre and is denoted by the Greek letter mu (pi). The particles of rubber in natural rubber latex vary in diameter from about 0.05 /unto 3 ptm. 

A test which is claimed to be a more reliable guide to the condition of a natural rubber latex than the KOH number. The test is performed by steam distillation of the latex and titration of the distillate with standard alkali solution. The VFA number is a measure of the state of degradation of the latex. 

Phenan thro line (182) can be used instead of thiocyanate to form a complex with Fe(III) ions resulting from the oxidation of Fe(II), and the measurement is made at 500 to 510 nm. The use of 182 has the advantage of stability in the presence of air and also of allowing the use of hydrocarbon solvents for increased solubility of certain analytes. The method was applied for determination of hydroperoxides in natural rubber and synthetic elastomers, in the range of 10 to 20 ppm active oxygen. The sensitivity can be improved to less than 1 ppm, depending on the color of the sample solution. ... 

Fig. 16a-

The most commonly reported physical properties of radiation cross-linked natural rubber and compounds made from it are modulus and tensile strength, obtained from stress-strain measurements. Figure 5.5 illustrates some of the results obtained from gum rubber and from a natural rubber compound reinforced by HAF carbon black. In Figure 5.6 the tensile strength of radiation cured gum is compared to that of vulcanizates cured by sulfur and by peroxide. ... 

The information on physical properties of radiation cross-linking of polybutadiene rubber and butadiene copolymers was obtained in a fashion similar to that for NR, namely, by stress-strain measurements. From Table 5.6, it is evident that the dose required for a full cure of these elastomers is lower than that for natural rubber. The addition of prorads allows further reduction of the cure dose with the actual value depending on the microstructure and macrostructure of the polymer and also on the type and concentration of the compounding ingredients, such as oils, processing aids, and antioxidants in the compound. For example, solution-polymerized polybutadiene rubber usually requires lower doses than emulsion-polymerized rubber because it contains smaller amount of impurities than the latter. Since the yield of scission G(S) is relatively small, particularly when oxygen is excluded, tensile... 

The effect of polymer-filler interaction on solvent swelling and dynamic mechanical properties of the sol-gel-derived acrylic rubber (ACM)/silica, epoxi-dized natural rubber (ENR)/silica, and polyvinyl alcohol (PVA)/silica hybrid nanocomposites was described by Bandyopadhyay et al. [27]. Theoretical delineation of the reinforcing mechanism of polymer-layered silicate nanocomposites has been attempted by some authors while studying the micromechanics of the intercalated or exfoliated PNCs [28-31]. Wu et al. [32] verified the modulus reinforcement of rubber/clay nanocomposites using composite theories based on Guth, Halpin-Tsai, and the modified Halpin-Tsai equations. On introduction of a modulus reduction factor (MRF) for the platelet-like fillers, the predicted moduli were found to be closer to the experimental measurements. 

Fig. 39 Improvement of physical properties of various rubbers through incorporation of clay or swollen clay 50% modulus (a), tensile strength (b), elongation at break (c), and the stress-strain plots for natural rubber (d). The strain was measured on the basis of clamp distance measurements...

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