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Hydrocarbons melting characteristics

Its charge transfer complexes with aromatic hydrocarbons have characteristic melting points and may be used for the identification and purification of the hydrocarbons. [Pg.406]

Aromatic hydrocarbon, halogen hydrocarbon General characteristics At room temperature, the polymer shows vulcanized rubber properties and exhibits thermoplasticity at elevated temperatures. It shows resin properties following increase in styrene concentration. When using trans-polybutadiene, it shows a shape memory tendency. It is possible to process while melted and is strong and has high-elasticity and good low-temperature characteristics. It also has exceptional acid resistance and alkali resistance. [Pg.1551]

Picrates, Picric acid combines with amines to yield molecular compounds (picrates), which usually possess characteristic melting points. Most picrates have the composition 1 mol amine 1 mol picric acid. The picrates of the amines, particularly of the more basic ones, are generally more stable than the molecular complexes formed between picric acid and the hydrocarbons (compare Section IV,9,1). [Pg.422]

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). [Pg.350]

Vapor grown carbon fiber (VGCF) is the descriptive name of a class of carbon fiber which is distinctively different from other types of carbon fiber in its method of production, its unique physical characteristics, and the prospect of low cost fabrication. Simply stated, this type of carbon fiber is synthesized from the pyrolysis of hydrocarbons or carbon monoxide in the gaseous state, in the presence of a catalyst in contrast to a melt-spinning process common to other types of carbon fiber. [Pg.139]

Tackifiers. The tackifiers usually are hydrocarbon resins (aliphatic C5, aromatic C9) or natural resins (polyterpenes, rosin and rosin derivates, tall oil rosin ester). They improve hot tack, wetting characteristics and open time and enhance adhesion. The content on tackifiers in a hot melt can be in the region of 10-25%. [Pg.1076]

These compounds are chemically and thermally stable and strain-free. These characteristics cause high melting points (m.p.) in comparison to other hydrocarbons. For instance, the m.p. of adamantane is estimated to be 269 °C, yet it sublimes easily, even at atmospheric pressure and room temperature. The melting point of diamantane is about 236.5 °C and the melting point of triamantane is estimated to be 221.5 °C. The available melting point data for diamondoids are reported in Table I. [Pg.212]

IR and Raman spectroscopic studies on films and powders of PDHS indicate that the hexyl side chains are crystallizing into a hydrocarbon type matrix (40). This is indicated by the presence of a number of sharp characteristic alkane bands which become dramatically broadened above the transition temperature. Similar changes are observed for n-hexane below and above the melting point. CPMAS 29Si NMR studies on PDHS also show that the rotational freedom of the side chains increases markedly above the transition temperature (41,42). All of the spectral evidence... [Pg.46]

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. [Pg.140]

The classes listed in Table 1-12 are families which exhibit the same regularity of boiling points, melting points, densities, and other properties seen in the hydrocarbon families we have already studied. Some of the families are named with characteristic suffixes while others have prefixes, or even separate words-in the names. For instance, alcohols are named with the suffix -ol. Ketones are named with the suffix -one. Amine and nitriles are named with the full suffix according to the family name. Ethers and halides usually have the full family name as a separate word, and nitro- and organometallic compounds have the prefix nitro- or the prefix corresponding to the hydrocarbon part of the organometallic molecule. [Pg.35]

Aroylation of an aromatic system by reaction with phthalic anhydride under Friedel-Crafts conditions yields the o-aroylbenzoic acid. These readily available compounds have characteristic melting points which make them useful as derivatives in the characterisation of aromatic hydrocarbons and of aryl halides (Section 9.6.3, p. 1238). [Pg.1007]

Non-Polymeric Materials. Waxes, soaps, greases, asphalts, oils. Complex mixtures of hydrocarbons of different molecular weight when treated to a common thermal history (such as slow program-cooling from above the melt) give complex but highly repeatable characteristic DSC melting profiles (16,17). In the absence of any other forensic evidence, these thermal profiles should be sufficiently specific and repeat-able to be definitive evidence. [Pg.130]

Camauba Wax Camauba wax contains a mixture of esters of acids and hydroxy-acids isolated from Brazilian camauba palm. It also contains various resins, hydrocarbons, acids, polyhydric alcohols, and water. It is available as lumps, powder, or flakes which are brown to pale yellow in color and possesses a characteristic odor. Carnauba wax is practically insoluble in water and melts at 80-88 °C. Being a hard material, it improves the stiffness of topical preparations [6],... [Pg.274]


See other pages where Hydrocarbons melting characteristics is mentioned: [Pg.112]    [Pg.9]    [Pg.21]    [Pg.507]    [Pg.708]    [Pg.77]    [Pg.326]    [Pg.463]    [Pg.966]    [Pg.387]    [Pg.44]    [Pg.71]    [Pg.188]    [Pg.361]    [Pg.173]    [Pg.1338]    [Pg.374]    [Pg.83]    [Pg.172]    [Pg.273]    [Pg.35]    [Pg.287]    [Pg.195]    [Pg.13]    [Pg.88]    [Pg.150]    [Pg.98]    [Pg.338]   
See also in sourсe #XX -- [ Pg.25 ]




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