Softening point hydrocarbon

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). 

As appHed to hydrocarbon resins, dsc is mainly used for the determination of glass-transition temperatures (7p. Information can also be gained as to the physical state of a material, ie, amorphous vs crystalline. As a general rule of thumb, the T of a hydrocarbon resin is approximately 50°C below the softening point. Oxidative induction times, which are also deterrnined by dsc, are used to predict the relative oxidative stabiHty of a hydrocarbon resin. 

Due to the fact that BF is a weaker Lewis acid than AlCl, stmcturaHy distinct resins are obtained upon the respective polymerization of a piperylenes-2-methyl-2-butene system with the two different Lewis acids. Much lower levels of branched olefin are required to achieve a softening point of <40° C with the BF catalyzed system (33,36). In fact, due to its weaker acidity, BF is not useful for producing high softening point resins based on C-5 hydrocarbon feeds. 

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. 

East India. Resins. The East India resins are related to the dammars, although they are older and harder. They are not obtained by tapping trees, but are collected where they are found, principally in Indonesia. Because they are semifossil resins, their softening points are high, ranging from about 110—130°C. The East India resins [9000-16-2] have low (20—30) acid numbers. They are soluble only in aryl hydrocarbons and hydrogenated aUphatic hydrocarbons, and are used primarily in coatings. 

Sandarac. This resin, which originates in Morocco, is a polar, acidic, hard resin with a softening point of 100—130°C, an acid number of 117—155, and a saponification number of 145—157. Sandarac [9000-57-1] is soluble in alcohols and insoluble in aryl and aUphatic hydrocarbons. It is used in varnishes and lacquers for coating paper, wood, and metal. 

Mastic. Most commercial mastic [61789-92-2] is collected on the Greek island of Chios, near the Turkish coast. It is a soft resin with a softening point of 55°C. It has an acid number of 50—70 and a saponification number of 62—90. It is soluble in alcohols and aryl hydrocarbons. Mastic is used in wood coatings, lacquers, adhesives, and printing inks. 

Coal tar is the condensation product obtained by cooling to approximately ambient temperature, the gas evolved in the destmctive distillation of coal. It is a black viscous Hquid denser than water and composed primarily of a complex mixture of condensed ring aromatic hydrocarbons. It may contain phenoHc compounds, aromatic nitrogen bases and their alkyl derivatives, and paraffinic and olefinic hydrocarbons. Coal-tar pitch is the residue from the distillation of coal tar. It is a black soHd having a softening point of 30—180°C (86—359°F). 

Compared with atactic polypropylene it has a lower softening point (less than 100°C compared with 154°C when assessed by ball and ring methods), has better resistance to subzero temperatures and is completely soluble in aliphatic hydrocarbons. The molecular mass of atactic polybut-l-ene is about twice that of an atactic polypropylene of similar melt viscosity. 

Many monomers have been copolymerised with ethylene using a variety of polymerisation systems, in some cases leading to commercial products. Copolymerisation of ethylene with other olefins leads to hydrocarbon polymers with reduced regularity and hence lower density, inferior mechanical properties, lower softening point and lower brittle point. 

Butadiene and styrene may be polymerised in any proportion. The Tfs of the copolymers vary in an almost linear manner with the proportion of styrene present. Whereas SBR has a styrene content of about 23.5% and is rubbery, copolymers containing about 50% styrene are leatherlike whilst with 70% styrene the materials are more like rigid thermoplastics but with low softening points. Both of these copolymers are known in the rubber industry as high-styrene resins and are usually used blended with a hydrocarbon rubber such as NR or SBR. Such blends have found use in shoe soles, car wash brushes and other mouldings but in recent times have suffered increasing competition from conventional thermoplastics and to a less extent the thermoplastic rubbers. 

Polymerization of raw feedstock. Aliphatic hydrocarbon resins. Raw feedstock contains straight-chain and cyclic molecules and mono- and diolefins. The most common initiator in the polymerization reaction is AICI3/HCI in xylene. The resinification consists of a two-stage polymerization in a reactor at 45°C and high pressure (10 MPa) for several hours. The resulting solution is treated with water and passed to distillation to obtain the aliphatic hydrocarbon resins. Several aliphatic hydrocarbon resins with different softening points can be adjusted. 

Unmodified aliphatic hydrocarbon resins softening point = 80-100°C, Gardner colour = 3.5-7. 

Aromatic hydrocarbon resins. The polymerization procedure and variables in the reactions of the aromatic hydrocarbon resins are similar to those for the coumarone-indene resins. However, the Cg feedstreams used in the polymerization of the aromatic hydrocarbon resins do not contain significant amounts of phenols or pyridine bases, so they are submitted directly to fractional distillation. Distillation produced more byproducts than light coal-tar oils. The aromatic hydrocarbon resins obtained have softening points between liquid and 125°C and Gardner colour of 6 to 11. By changing distillation conditions, aromatic hydrocarbon resins with softening points between 65 and 170°C and Gardner colour of 5 to 10 can also be obtained. 

Uintaite is described in Kirk-Othmer [1329]. Typical uintaite used in drilling fluids is mined from an area around Bonanza, Utah and has a specific gravity of 1.05 with a softening point ranging from 190° C to 205° C, although a lower softening point (165° C) material is sometimes used. It has a low acid value, a zero iodine number, and is soluble or partially soluble in aromatic and aliphatic hydrocarbons, respectively. 

Due to its cheapness, transparency and rigidity attempts were made to develop copolymers with better heat resistance and toughness. Styrene-acrylonitrile copolymers containing 20-30 per cent acrylonitrile have higher softening point and better impact strength. They are transparent and resistant to hydrocarbon and oils. 

The copolymer is having a higher softening point and improved impact strength than the linear polystyrene. Due to the polar nature of acrylonitrile, the copolymers are some what more resistant to hydrocarbons and oils than polystyrene. 

If sufficient crosslinks of this type occur in the polymeric hydrocarbon, all molecules are joined in a single giant molecule. The characteristic property of a crosslinked polymer is its intractibility above the softening point or melting point that is normally observed in the uncrosslinked base polymer. 

When coal is heated in a vacuum, the plastic range is generally reduced substantially, perhaps because of the rapid evaporation of the bituminous hydrocarbons that are reputedly responsible for the fluidity of the plastic coal. Heating coal to the plastic range followed by rapid cooling yields coal with a lower softening point (if plasticized a second time), and this has been ascribed to the presence of liquid in the coal that arose from the first heating. 

The generic name hydrocarbon resins designates several families of low molar mass polymers (M from 600 to 104) obtained by polymerization of petroleum, coal tar, and turpentine distillates [80-82], In most cases, these products are obtained by cationic polymerization of mixtures either of aliphatic and/or aromatic mono and diolefins present in the more or less enriched Cs and C9 feedstreams, or of pure aromatic monomers generally of the styrene type. They are complex mixtures of polymers ranging from viscous liquids and tacky fluids to hard, brittle thermoplastics, and are used as additives in adhesives, printing inks, rubbers, coatings, etc. [80-82], They are obviously amorphous and are characterized by their softening point (0 to —150° C), determined by standardized methods (i.e.,... 

---