Molecular iodine

Now the moii t ui.u heat at i oiistaut pressttrp of any moiutomir gas (I) t uny temjwiuitue is c, c abates jK r degiee. Also the molecular beat oj iodine (molecular) 18, sx shown by experiment to he given by the expression ... [Pg.391]

R. Sahia, V. Singh, and R. K. Verma, Role of Dielectric Constant on Stoichiometry of Some Iodine Molecular Complexes and Their Transformation into Ion Pairs, Indian J. Chem. Sec. A 20A(10), 1017 (1981). [Pg.535]

Based on the obtained data we conclude that the zwitterionic form of glycine significantiy influences the iodine-triiodide equilibrium. In the presence of glycine in a solution containing potassium halogenides and molecular iodine, molecular iodine and triiodide complexes can be detected both in the UV and IR spectra. The calculated spectral characteristics for the complexes of molecular iodine and triiodide provide the most complete assignment and description of the experimental UV-IR characteristics for the system (b). [Pg.291]

The recombinations of chlorine atoms in molecular chlorine [57] and of iodine atoms in the system atomic iodine-molecular iodine-carbon dioxide [58] have been investigated under critical conditions. The concentration of the atomic species is not measured directly, but assumed to be directly proportional to the depression in the critical temperature of the reacting mixture, as ascertained from the disappearance of the liquid-vapour meniscus. [Pg.63]

Lagorce, J.F., Buxeraud, J., Jambut-AbsU, A.C. and Raby, C. (1990) Spectroscopic analysis of iodinated molecular complexes of thiazole and thiazoline derivatives. Hetewcycles, 31, 1609-1615. [Pg.315]

Takemura K, Minomura S, Shimomura O, Fu]ii Y and Axe J D 1982 Structural aspects of solid iodine associated with metallization and molecular dissociation under high pressure Phys. Rev. B 26 998... [Pg.1962]

X resonance series of molecular iodine J. Chem. Phys. 40 1934—44... [Pg.2087]

To decide which component should be employed for the calculation of the yield of ethyl iodide, the weights of the reactants are first divided by the appropriate atomic or molecular weight in order to obtain the number of gram atoms or gram mols actually used. The equation shows that the alcohol and iodine react in the ratio of 5 5 or 1 1. Inspection of the results clearly shows that the alcohol is present in about 20 per... [Pg.203]

The "time of flight" mass spectrometer has been used to confirm that this highly radioactive halogen behaves chemically very much like other halogens, particularly iodine. Astatine is said to be more metallic than iodine, and, like iodine, it probably accumulates in the thyroid gland. Workers at the Brookhaven National Laboratory have recently used reactive scattering in crossed molecular beams to identify and measure elementary reactions involving astatine. [Pg.150]

The 4,5-dihalogenothiazoles are obtained by cyclization-halogenation reactions as show in scheme 12 (3). 2-Acetamido-4,5-diiodothiazole has been obtained by Hurd and Wehrmeister (80). The triiodothiazole can be prepared by iodination by molecular iodine of the mercuric complex of 2-iodothiazole following the Travagli method (81). [Pg.575]

Simple fragmentation of the molecular ion of iodobenzene gives a fragment ion, CjH,. The difference in measured masses between the molecular and fragment ions gives the mass of the ejected neutral iodine atom. [Pg.271]

To prevent such release, off gases are treated in Charcoal Delay Systems, which delay the release of xenon and krypton, and other radioactive gases, such as iodine and methyl iodide, until sufficient time has elapsed for the short-Hved radioactivity to decay. The delay time is increased by increasing the mass of adsorbent and by lowering the temperature and humidity for a boiling water reactor (BWR), a typical system containing 211 of activated carbon operated at 255 K, at 500 K dewpoint, and 101 kPa (15 psia) would provide about 42 days holdup for xenon and 1.8 days holdup for krypton (88). Humidity reduction is typically provided by a combination of a cooler-condenser and a molecular sieve adsorbent bed. [Pg.285]

If the spent fuel is processed in a nuclear fuel reprocessing plant, the radioactive iodine species (elemental iodine and methyl iodide) trapped in the spent fuel elements ate ultimately released into dissolver off gases. The radioactive iodine may then be captured by chemisorption on molecular sieve 2eohtes containing silver (89). [Pg.285]

Iodine reacts with hydrocarbons to form iodine compounds, but compared to the other halogens, the equiUbria are unfavorable because the displacement step with the iodine atom is endothermic, requiring 4066.3 J (971.9 cal) for methane and 799.9 J (191.2 cal) for toluene. Hydrogen iodide can be used to reduce an alkah iodide to hydrocarbon plus molecular iodine. [Pg.361]

Naphthenic acids occur ia a wide boiling range of cmde oil fractions, with acid content increa sing with boiling point to a maximum ia the gas oil fraction (ca 325°C). Jet fuel, kerosene, and diesel fractions are the source of most commercial naphthenic acid. The acid number of the naphthenic acids decreases as heavier petroleum fractions are isolated, ranging from 255 mg KOH/g for acids recovered from kerosene and 170 from diesel, to 108 from heavy fuel oil (19). The amount of unsaturation as indicated by iodine number also increases in the high molecular weight acids recovered from heavier distillation cuts. [Pg.510]

Chlorine heptoxide is more stable than either chlorine monoxide or chlorine dioxide however, the CX C) detonates when heated or subjected to shock. It melts at —91.5°C, bods at 80°C, has a molecular weight of 182.914, a heat of vapori2ation of 34.7 kj/mol (8.29 kcal/mol), and, at 0°C, a vapor pressure of 3.2 kPa (23.7 mm Hg) and a density of 1.86 g/mL (14,15). The infrared spectmm is consistent with the stmcture O CIOCIO (16). Cl O decomposes to chlorine and oxygen at low (0.2—10.7 kPa (1.5—80 mm Hg)) pressures and in a temperature range of 100—120°C (17). It is soluble in ben2ene, slowly attacking the solvent with water to form perchloric acid it also reacts with iodine to form iodine pentoxide and explodes on contact with a flame or by percussion. Reaction with olefins yields the impact-sensitive alkyl perchlorates (18). [Pg.65]

There are no universally accepted wet analytical methods for the characteri2ation of quaternary ammonium compounds. The American Oil Chemists Society (AOCS) has estabhshed, however, a number of appHcable tests (180). These include sampling, color, moisture, amine value, ash, iodine value, average molecular weight, pH, and flash point. [Pg.378]

Name Company Name Molecular weight Iodine content, % Solubihty ia water, % wt /vol Viscosity, 300 mg/mL, cps... [Pg.463]

Composition. Shellac is primarily a mixture of aUphatic polyhydroxy acids in the form of lactones and esters. It has an acid number of ca 70, a saponification number of ca 230, a hydroxyl number of ca 260, and an iodine number of ca 15. Its average molecular weight is ca 1000. Shellac is a complex mixture, but some of its constituents have been identified. Aleuritic acid, an optically inactive 9,10,16-trihydroxypalmitic acid, has been isolated by saponification. Related carboxyflc acids such as 16-hydroxy- and 9,10-dihydroxypalmitic acids, also have been identified after saponification. These acids may not be primary products of hydrolysis, but may have been produced by the treatment. Studies show that shellac contains carboxyflc acids with long methylene chains, unsaturated esters, probably an aliphatic aldehyde, a saturated aliphatic ester, a primary alcohol, and isolated or unconjugated double bonds. [Pg.141]

An excess of crotonaldehyde or aUphatic, ahcyhc, and aromatic hydrocarbons and their derivatives is used as a solvent to produce compounds of molecular weights of 1000—5000 (25—28). After removal of unreacted components and solvent, the adduct referred to as polyester is decomposed in acidic media or by pyrolysis (29—36). Proper operation of acidic decomposition can give high yields of pure /n j ,/n7 j -2,4-hexadienoic acid, whereas the pyrolysis gives a mixture of isomers that must be converted to the pure trans,trans form. The thermal decomposition is carried out in the presence of alkaU or amine catalysts. A simultaneous codistillation of the sorbic acid as it forms and the component used as the solvent can simplify the process scheme. The catalyst remains in the reaction batch. Suitable solvents and entraining agents include most inert Hquids that bod at 200—300°C, eg, aUphatic hydrocarbons. When the polyester is spHt thermally at 170—180°C and the sorbic acid is distilled direcdy with the solvent, production and purification can be combined in a single step. The solvent can be reused after removal of the sorbic acid (34). The isomeric mixture can be converted to the thermodynamically more stable trans,trans form in the presence of iodine, alkaU, or sulfuric or hydrochloric acid (37,38). [Pg.283]

PuUy hydroly2ed poly(vinyl alcohol) and iodine form a complex that exhibits a characteristic blue color similar to that formed by iodine and starch (171—173). The color of the complex can be enhanced by the addition of boric acid to the solution consisting of iodine and potassium iodide. This affords a good calorimetric method for the deterrnination of poly(vinyl alcohol). Color intensity of the complex is effected by molecular weight, degree of... [Pg.481]

C-21 dicarboxyhc acids are produced by Westvaco Corporation in Charleston, South Carolina in multimillion kg quantities. The process involves reaction of tall oil fatty acids (TOFA) (containing about 50% oleic acid and 50% hnoleic acid) with acryhc acid [79-10-7] and iodine at 220—250°C for about 2 hours (90). A yield of C-21 as high as 42% was reported. The function of the iodine is apparendy to conjugate the double bond in linoleic acid, after which the acryhc acid adds via a Diels-Alder type reaction to form the cycHc reaction product. Other catalysts have been described and include clay (91), palladium, and sulfur dioxide (92). After the reaction is complete, the unreacted oleic acid is removed by distillation, and the cmde C-21 diacid can be further purified by thin film distillation or molecular distillation. [Pg.64]

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