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Crystalline melting point Crystallinity

Pure hydroxylamine is a crystalline solid of low melting point (306 K) but is rarely prepared because it decomposes above 288 K... [Pg.222]

Being crystalline compounds which usually have sharp melting-points, they are used to characterise the parent aldehydes and ketones. [Pg.93]

The melting points of some crystalline derivatives of a number of selected aliphatic aldehydes are collected in Table 111,70. [Pg.333]

Drop 1 g. of sodium into 10 ml. of ethyl alcohol in a small flask provided with a small water condenser heat the mixture until all the sodium has dissolved. Cool, and add 1 g. of the ester and 0-5 ml. of water. Frequently the sodium salt of the acid will be deposited either at once or after boiling for a few minutes. If this occurs, filter oflF the solid at once, wash it with a little absolute ethyl alcohol (or absolute methylated spirit), and convert it into the p-bromophenacyl ester, p-nitro-benzyl ester or S-benzyl-tso-thiuronium salt (for experimental details, see Section 111,85). If no solid separates, continue the boiling for 30-60 minutes, boil oflF the alcohol, allow to cool, render the product just neutral to phenolphthalein with dilute sulphuric or hydrochloric acid, convert the sodium salt present in solution into a crystalline derivative (Section 111,85), and determine its melting point. [Pg.391]

Of the crystalline derivatives of thiols, those formed with 3 5-dinitro-benzoyl chloride are not very satisfactory since they have, in general lower melting points than those of the corresponding alcohols (compare Section 111,27,7) and do not diflfer widely from ethyl to n-heptyl. The best results are obtained with 2 4-dinitrochlorobenzene. [Pg.500]

The benzoyl compounds frequently occlude traces of unchanged benzoyl chloride, which thus escape hydrolysis by the caustic alkali it is therefore advisable, wherever possible, to recrystaUise the benzoyl derivatives from methyl, or ethyl alcohol or methylated spirit, since these solvents will esterify the unchanged chloride and so remove the latter from the recrystalKsed material. Sometimes the benzoyl compound does not crystallise well this difficulty may frequently be overcome by the use of p-nitrobenzoyl chloride or 3 5-dinitro-benzoyl chloride, which usually give highly crystalline derivatives of high melting point (see Section IV,114j. [Pg.582]

These are crystalline compounds with sharp melting points, and possess the further advantage that their equivalent weights may be determined by dissolving in dilute alcohol and titrating with standard alkali. Nitro-phenols, however, give unsatisfactory derivatives. [Pg.683]

Sulphonic acids. The aromatic sulphonic acids and their alkali metal salts are soluble in water, but insoluble in ether (Solubility Group II). They are best characterised by conversion into crystalline S-benzyl-iso-thiuronium salts (see Section IV,33,2 and 111,85,5), which possess characteristic melting points. A more time-consuming procedure is to treat the well-dried acid or... [Pg.1077]

The refractory industry has found chromite useful for forming bricks and shapes, as it has a high melting point, moderate thermal expansion, and stability of crystalline structure. [Pg.69]

Properties. The DPXs are all crystalline soHds melting points and densities are given in Table 1. Their solubiUty in aromatic hydrocarbons is Limited. At 140°C, the solubiUty of DPXN in xylene is only about 10%. DPXC is more readily soluble in chlorinated solvents, eg, in methylene chloride at 25°C its solubihty is 10%. In contrast, the corresponding figure for DPXN is 1.5%. [Pg.431]

Acetaldehyde can be isolated and identified by the characteristic melting points of the crystalline compounds formed with hydrazines, semicarbazides, etc these derivatives of aldehydes can be separated by paper and column chromatography (104,113). Acetaldehyde has been separated quantitatively from other carbonyl compounds on an ion-exchange resin in the bisulfite form the aldehyde is then eluted from the column with a solution of sodium chloride (114). In larger quantities, acetaldehyde may be isolated by passing the vapor into ether, then saturating with dry ammonia acetaldehyde—ammonia crystallizes from the solution. Reactions with bisulfite, hydrazines, oximes, semicarb azides, and 5,5-dimethyl-1,3-cyclohexanedione [126-81 -8] (dimedone) have also been used to isolate acetaldehyde from various solutions. [Pg.53]

The many commercially attractive properties of acetal resins are due in large part to the inherent high crystallinity of the base polymers. Values reported for percentage crystallinity (x ray, density) range from 60 to 77%. The lower values are typical of copolymer. Poly oxymethylene most commonly crystallizes in a hexagonal unit cell (9) with the polymer chains in a 9/5 helix (10,11). An orthorhombic unit cell has also been reported (9). The oxyethylene units in copolymers of trioxane and ethylene oxide can be incorporated in the crystal lattice (12). The nominal value of the melting point of homopolymer is 175°C, that of the copolymer is 165°C. Other thermal properties, which depend substantially on the crystallization or melting of the polymer, are Hsted in Table 1. See also reference 13. [Pg.56]

Because of the high melt viscosity of polyolefins, normal spinning melt temperatures are 240—310°C, which is 80—150°C above the crystalline melting point. Because of the high melt temperatures used for polyolefin fiber spinning, thermal stabilizers such as substituted hindered phenols are added. In the presence of pigments, the melt temperature must be carefully controlled to prevent color degradation and to obtain uniform color dispersion. [Pg.317]

In some appHcations the high heat stabiHty of the micropowder can be utilized over a reasonably wide temperature range. A maximum service temperature is normally 260°C, provided the crystalline melting point is between 320 and 335°C. Exposure above 300°C leads to degradation and possible evolution of toxic decomposition products. [Pg.355]

The equimolar copolymer of ethylene and tetrafluoroethylene is isomeric with poly(vinyhdene fluoride) but has a higher melting point (16,17) and a lower dielectric loss (18,19) (see Fluorine compounds, organic-poly(VINYLIDENE fluoride)). A copolymer with the degree of alternation of about 0.88 was used to study the stmcture (20). Its unit cell was determined by x-ray diffraction. Despite irregularities in the chain stmcture and low crystallinity, a unit cell and stmcture was derived that gave a calculated crystalline density of 1.9 g/cm. The unit cell is befleved to be orthorhombic or monoclinic (a = 0.96 nm, b = 0.925 nm, c = 0.50 nm 7 = 96%. [Pg.365]

The melting point of commercial Teflon PEA is 305°C, ie, between those of PTEE and EEP. Second-order transitions are at —100, —30, and 90°C, as determined by a torsion pendulum (21). The crystallinity of the virgin resin is 65—75%. Specific gravity and crystallinity increase as the cooling rate is reduced. An ice-quenched sample with 48% crystallinity has a specific gravity of 2.123, whereas the press-cooled sample has a crystallinity of 58% and a specific gravity of 2.157. [Pg.374]

Stabilization of the Cellular State. The increase in surface area corresponding to the formation of many ceUs in the plastic phase is accompanied by an increase in the free energy of the system hence the foamed state is inherently unstable. Methods of stabilizing this foamed state can be classified as chemical, eg, the polymerization of a fluid resin into a three-dimensional thermoset polymer, or physical, eg, the cooling of an expanded thermoplastic polymer to a temperature below its second-order transition temperature or its crystalline melting point to prevent polymer flow. [Pg.404]

Meclizine Hydrochloride. Pipera2ine Antivert, and Bonine are trade names for mech2ine dihydrochloride monohydrate [31884-77-2] (20). It is a white or slightly yellowish crystalline powder with a slight odor, no taste, and a melting point of 217—224°C. The hydrochloride is practically insoluble in water and ether. It is freely soluble in chloroform, pyridine, methylacetamide, and mild acid alcohol—water mixtures, and is slightly soluble in dilute acids or alcohol. See Reference 16 for synthesis. [Pg.204]


See other pages where Crystalline melting point Crystallinity is mentioned: [Pg.182]    [Pg.116]    [Pg.306]    [Pg.314]    [Pg.2729]    [Pg.2898]    [Pg.164]    [Pg.336]    [Pg.438]    [Pg.439]    [Pg.586]    [Pg.21]    [Pg.75]    [Pg.79]    [Pg.129]    [Pg.342]    [Pg.342]    [Pg.455]    [Pg.586]    [Pg.334]    [Pg.433]    [Pg.439]    [Pg.440]    [Pg.132]    [Pg.323]    [Pg.473]    [Pg.534]    [Pg.312]    [Pg.348]    [Pg.350]    [Pg.353]    [Pg.379]    [Pg.379]    [Pg.380]    [Pg.331]   


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Crystalline melting

Crystalline melting point method

Crystalline melting point monomer/polymer systems

Crystalline melting point, molecular

Crystalline melting point, molecular structure, dependence

Crystalline point

Crystalline polymers equilibrium melting point

Crystalline salts melting point

Crystallinity melting

Factors Affecting the Crystalline Melting Point

Glass transition temperature and crystalline melting point

Liquid crystalline polymers melting point, effect

Melting point crystalline

Melting point crystalline

Melting point polymer crystalline

Nylon crystalline melting point

Polyethylene crystalline melting point

Polypropylene crystalline melting point

Polystyrene crystalline melting point

The Crystalline Melting Point

The Relationship between Crystalline Melting Point and

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