Parameters of resins

G-5—G-9 Aromatic Modified Aliphatic Petroleum Resins. Compatibihty with base polymers is an essential aspect of hydrocarbon resins in whatever appHcation they are used. As an example, piperylene—2-methyl-2-butene based resins are substantially inadequate in enhancing the tack of 1,3-butadiene—styrene based random and block copolymers in pressure sensitive adhesive appHcations. The copolymerization of a-methylstyrene with piperylenes effectively enhances the tack properties of styrene—butadiene copolymers and styrene—isoprene copolymers in adhesive appHcations (40,41). Introduction of aromaticity into hydrocarbon resins serves to increase the solubiHty parameter of resins, resulting in improved compatibiHty with base polymers. However, the nature of the aromatic monomer also serves as a handle for molecular weight and softening point control. 

Table V. Solubility Parameters of Resin Cleanup Solvents...

Parameters of Resins. Some of the manufacturers of the low molecular weight hydrocarbon resins have offered estimates (5, 6) of solubility parameters of some of their resins. These values have been established by determining the solvents (in one case at 50% solids) for the... 

The solubility parameter of resins, solvents, and plasticizers is a valuable index to their behavior in many applications. Coupled with the phase diagram for the resin-plasticizer system, it is possible to determine the area where optimum physical properties are encountered. In this area precise control must be maintained. The parameters of many industrial materials are often not known accurately enough to be useful. However, specific solubility tests are used to give the desired degree of control. 

The rate of asphaltene adsorption is greater than desorption rate for studied concentration. Gibbs adsorption energy values define character of adsorption as physical, not chemical. Rate of asphaltene adsorption is less then resins (in two orders) reported earlier (Balabin Syunyaev, 2008). Parameters of resin adsorption from benzene solutions on quartz... 

Table 4. Adsorption parameters of resins on quartz sand.

Most hydrocarbon resins are composed of a mixture of monomers and are rather difficult to hiUy characterize on a molecular level. The characteristics of resins are typically defined by physical properties such as softening point, color, molecular weight, melt viscosity, and solubiHty parameter. These properties predict performance characteristics and are essential in designing resins for specific appHcations. Actual characterization techniques used to define the broad molecular properties of hydrocarbon resins are Fourier transform infrared spectroscopy (ftir), nuclear magnetic resonance spectroscopy (nmr), and differential scanning calorimetry (dsc). 

Solubility Parameter. CompatibiHty between hydrocarbon resins and other components in an appHcation can be estimated by the Hildebrand solubiHty parameter (2). In order for materials to be mutually soluble, the free energy of mixing must be negative (3). The solubiHty of a hydrocarbon resin with other polymers or components in a system can be approximated by the similarities in the solubiHty parameters of the resin and the other materials. Tme solubiHty parameters are only available for simple compounds and solvents. However, parameters for more complex materials can be approximated by relative solubiHty comparisons with substances of known solubiHty parameter. 

In order to increase the solubiUty parameter of CPD-based resins, vinyl aromatic compounds, as well as other polar monomers, have been copolymerized with CPD. Indene and styrene are two common aromatic streams used to modify cyclodiene-based resins. They may be used as pure monomers or contained in aromatic steam cracked petroleum fractions. Addition of indene at the expense of DCPD in a thermal polymerization has been found to lower the yield and softening point of the resin (55). CompatibiUty of a resin with ethylene—vinyl acetate (EVA) copolymers, which are used in hot melt adhesive appHcations, may be improved by the copolymerization of aromatic monomers with CPD. As with other thermally polymerized CPD-based resins, aromatic modified thermal resins may be hydrogenated. 

Physical Properties. LLDPE is a sernicrystaUine plastic whose chains contain long blocks of ethylene units that crystallize in the same fashion as paraffin waxes or HDPE. The degree of LLDPE crystallinity depends primarily on the a-olefin content in the copolymer (the branching degree of a resin) and is usually below 40—45%. The principal crystalline form of LLDPE is orthorhombic (the same as in HDPE) the cell parameters of nonbranched PE are a = 0.740 nm, b = 0.493 nm, and c (the direction of polymer chains) = 0.2534 nm. Introduction of branching into PE molecules expands the cell slightly thus a increases to 0.77 nm and b to around 0.50 nm. 

Polymorphism. Many crystalline polyolefins, particularly polymers of a-olefins with linear alkyl groups, can exist in several polymorphic modifications. The type of polymorph depends on crystallisa tion conditions. Isotactic PB can exist in five crystal forms form I (twinned hexagonal), form II (tetragonal), form III (orthorhombic), form P (untwinned hexagonal), and form IP (37—39). The crystal stmctures and thermal parameters of the first three forms are given in Table 3. Form II is formed when a PB resin crystallises from the melt. Over time, it is spontaneously transformed into the thermodynamically stable form I at room temperature, the transition takes about one week to complete. Forms P, IP, and III of PB are rare they can be formed when the polymer crystallises from solution at low temperature or under pressure (38). Syndiotactic PB exists in two crystalline forms, I and II (35). Form I comes into shape during crystallisation from the melt (very slow process) and form II is produced by stretching form-1 crystalline specimens (35). 

On the commercial scale silicone resins are prepared batchwise by hydrolysis of a blend of chlorosilanes. In order that the final product shall be cross-linked, a quantity of trichlorosilanes must be incorporated into the blend. A measure of the functionality of the blend is given by the R/Si ratio (see Section 29.3). Whereas a linear polymer will have an R/Si ratio of just over 2 1, the ratio when using trichlorosilane alone will be 1 1. Since these latter materials are brittle, ratios in the range 1.2 to 1.6 1 are used in commercial practice. Since chlorophenylsilanes are also often used, the CH3/CgH5 ratio is a further convenient parameter of use in classifying the resins. 

The crowning development in MW determination was the invention of gel permeation chromatography, the antecedents of which began in 1952 and which was finally perfected by Moore (1964). A column is filled with pieces of cross-linked macroporous resin and a polymer solution (gel) is made to flow through the column. The polymer solute permeates the column more slowly when the molecules are small, and the distribution of molecules after a time is linked not only to the average MW but also, for the first time with these techniques, to the vital parameter of MW distribution. 

Solubility of resins can be predicted in a similar way as for the solubility of polychloroprene rubbers in a solvent mixture (see Section 5.5) by means of solubility diagrams (plots of the hydrogen bonding index (y) against the solubility parameter (5). Another more simple way to determine the solubility of resins is the determination of the cloud point, the aniline and the mixed aniline points. 

The penetration behavior of resins into the wood surface also is influenced by various parameters, like wood species, amount of glue spread, press temperature and pressure and hardening time. The temperature of the wood surface and of the glue line and hence the viscosity of the resin (which itself also depends on the already reached degree of hardening) influence the penetration behavior of the resin [79]. 

Multi-walled CNTs (MWCNTs) are produced by arc discharge between graphite electrodes but other carbonaceous materials are always formed simultaneously. The main by-product, nanoparticles, can be removed utilizing the difference in oxidation reaction rates between CNTs and nanoparticles [9]. Then, it was reported that CNTs can be aligned by dispersion in a polymer resin matrix [10]. However, the parameters of CNTs are uncontrollable, such as the diameter, length, chirality and so on, at present. Furthermore, although the CNTs are observed like cylinders by transmission electron microscopy (TEM), some reports have pointed out the possibility of non-cylindrical structures and the existence of defects [11-14]. 

In our report147, the thermodynamic parameters, AG, AW, and AS of the reaction in the presence of resins and in their absence were compared in detail. 

Table 2. The values of the characteristic parameters of a series of E-glass fiber, epoxy resin unidirectional composites for various fiber volume contents t>f... 

The final structure of resins produced depends on the reaction condition. Formaldehyde to phenol (F/P) and hydroxyl to phenol (OH/P) molar ratios as well as ruction temperahne were the most important parameters in synthesis of resols. In this study, the effect of F/P and OH/P wt%, and reaction temperature on the chemical structure (mono-, di- and trisubstitution of methyrol group, methylene bridge, phenolic hemiformals, etc.) was studied utilizing a two-level full factorial experimental design. The result obtained may be applied to control the physical and chemical properties of pre-polymer. 

The frequency of fluid oscillation at which levitation takes place is plotted in Fig. 40 against the corresponding amplitude A of oscillation, the asymmetry factor ka or ratio of the duration of the downstroke to that of the upstroke, and the resin particle diameter d. From these experimental data, the three parameters of the equation were correlated to the particle diameter ... 

As shown in Fig. 4.1, resin feedstocks have a considerable level of interparticle space that is occupied by air. This level of space and thus the bulk density of the feedstock depend on the temperature, pressure, pellet (or powder) shape, resin type, and the level and shape of the recycle material. For a specific resin feedstock, the bulk density Increases with both temperature and the applied pressure. Understanding the compaction behavior of a resin feedstock is essential for both screw design and numerical simulation of the solids-conveying and melting processes. Screw channels must be able to accommodate the change in the bulk density to mitigate the entrainment of air and the decomposition of resin at the root of the screw. Typically, screw channels are set by using an acceptable compression ratio and compression rate for the resin. These parameters will be discussed in Section 6.1. 

Table VII summarizes the solubility parameters of MEK, the CTBN elastomers, and an epoxy resin of similar EEW.

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