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Mercury hydrocarbons

The success of this equation was shown from the start (Fowkes, 1964) as it was illustrated that experimental liquid-liquid interfacial tension data for ten mercury-hydrocarbon mixtures and for eight water-hydrocarbon mixtures resulted to more or less unique values for the dispersion contribution of mercury and water, respectively (see Example 3.3). Moreover, these values are in agreement with those estimated from theoretical considerations. [Pg.323]

Despite its simplicity, many success stories have been presented. For example, as already mentioned, using hquid—hquid interfacial tension data for several different mercury—hydrocarbons and water-alkanes, we can estimate ahnosf unique contributions for the dispersion surface tension of mercury (201 mN m ) and water (21.9 mN m ) (Hiemenz and Rajagopalan, 1997 Fowkes, 1964, 1980). These values appear to be reasonable and moreover when used to predict the interfacial tension of water-mercury, quite good agreement is obtained (see Example 3.3 and Problem 3.5). In addition to the success for hquid-hquid interfaces, the Fowkes equation has been used for solid interfaces with good results. As shown in Chapter 6, when combined with the Young equation, we obtain ... [Pg.323]

Mercury(II) oxide Chlorine, hydrazine hydrate, hydrogen peroxide, hypophosphorous acid, magnesium, phosphorus, sulfur, butadiene, hydrocarbons, methanethiol... [Pg.1209]

Vinyl acetate (ethenyl acetate) is produced in the vapor-phase reaction at 180—200°C of acetylene and acetic acid over a cadmium, 2inc, or mercury acetate catalyst. However, the palladium-cataly2ed reaction of ethylene and acetic acid has displaced most of the commercial acetylene-based units (see Acetylene-DERIVED chemicals Vinyl polymers). Current production is dependent on the use of low cost by-product acetylene from ethylene plants or from low cost hydrocarbon feeds. [Pg.393]

Bromobenzene. -The replacement of hydrogen by the halogens Cl and Br, in the nucleus of aromatic hydrocarbons, is assisted by the presence of a halogen carriei, the action of which lias been referred to in the Note on the piepaiations of chlor- and bioin-acetic acids, p. 252. Iodine, iion, iron and alupiinium chlorides and bromides, the aluminium-mercury... [Pg.271]

Hydrocarbon A has the formula C9HI2 and absorbs 3 equivalents of H to yield B, C9H]g, when hydrogenated over a Pd/C catalyst. On treatment of A with aqueous H2S04 in the presence of mercury(d), two isomeric ketones, C and D, are produced. Oxidation of A with KMn04 gives a mixture of acetic acid (CH3C02H) and the tricarboxylic acid E. Propose structures for compounds A-D, and write the reactions. [Pg.284]

The gas-phase photolysis of 2-furaldehyde in the it -n and ir <-it transitions76 proceeds with fragmentation to CO, furan and C3-hydrocarbons, but a certain amount of resinification is also noted (about 5% quantum yield with excitation of the it - n transition). The latter observation prompted a study of the vacuum liquid-phase photolysis by sunlight or by light from a medium-pressure mercury arc at room temperature24 7S. The resin obtained was submitted to fractionation and structural analysis. On the basis of the results obtained and other mechanistic evidence, the following sequence of events was postulated for the photopolymerization ... [Pg.67]

The next eight chapters will be devoted to the ecotoxicology of groups of compounds that have caused concern on account of their real or perceived environmental effects and have been studied both in the laboratory and in the field. These are predominantly compounds produced by humans. However, a few of them, for example, methyl mercury, methyl arsenic, and polycyclic aromatic hydrocarbons (PAHs), are also naturally occurring. In this latter case, there can be difficulty in distinguishing between human and natural sources of harmful chemicals. [Pg.99]

Koeman, J.H. and van Genderen, H. (1970). Tissue levels in animals and effects caused by chlorinated hydrocarbon insecticides, chlorinated biphenyls, and mercury in the marine environment along the Netherlands coast. FAO Technical Conference on Marine Pollution. Rome, December 1970. [Pg.356]

The photocatalytic experiments were performed in a horizontal quartz tube which it have TiOi. Illumination was provided by 500 W mercury lamps, located above the horizontal quartz tube. The reactant was 0.1% (v/v) ethylene in air. In case of Photo-Catalyst test, reactor effluent samples were taken at 30 min intervals and analyzed by GC. The composition of hydrocarbons in the feed and product stream was analyzed by a Shimadzu GC14B (VZIO) gas chromatograph equipped with a flame ionization detector. In all case, steady state was reached within 3 h. [Pg.718]

The CH4/CI2 mixture is explosive if it contains more than 20% of chlorine. If mercury oxide is present, the reaction is very violent. The accidents mentioned below deal with saturated hydrocarbons. [Pg.239]

Bishop CA, Koster MD, Chek AA, HusseU DJT, Jock K. 1995a. Chlorinated hydrocarbons and mercury in sediments, red-winged blackbirds Agelaius phoeniceus) and tree swallows (Tachycineta bicolor) from wetlands in the Great Lakes-St. Lawrence River basin. Environ Toxicol Chem 14 491-501. [Pg.168]

Baldrian, P., der Wiesche, C., Gabriel, J., Nerud, E, and Zadrazil, F., Influence of cadmium and mercury on activities of ligninolytic enzymes and degradation of polycyclic aromatic hydrocarbons by Pleurotus ostreatus in soil, Appl Environ Microbiol, 66 (6), 2471-2478, 2000. [Pg.426]

Asbestos fibers, dissolved chlorine, dissolved hydrogen, sodium chloride lead, chlorinated organic compound Lead, chlorinated organic compound, such as methylene chloride and hexachlorinated benzenes Mercury, asbestos fibers, chlorinated hydrocarbons Hypochlorite... [Pg.925]

The wastewater generated in the membrane cell and other process wastewaters in the cell are generally treated by neutralization.28 Other pollutants similar to those in mercury and diaphragm cells are treated in the same process stated above. Ion exchange and xanthate precipitation methods can be applied in this process to remove the metal pollutants, while incineration can be applied to eliminate some of the hydrocarbons. The use of modified diaphragms that resist corrosion and degradation will help in reducing the amount of lead, asbestos, and chlorinated hydrocarbon in the wastewater stream from the chlor-alkali industry.28... [Pg.926]

The rule proposes emission standards for dioxins, furans, mercury, cadmium, lead, PM, hydrochloric acid, chlorine, carbon monoxide, hydrocarbons, and several low-volatile metals. It also proposes a new comparable fuels exclusion and makes significant changes to the existing combustion regulations. [Pg.978]

Acetone Acetylene Alkali and alkaline earth metals, e.g. sodium, potassium, lithium, magnesium, calcium, powdered aluminium Anhydrous ammonia Concentrated nitric and sulphuric acid mixtures Chlorine, bromine, copper, silver, flourine or mercury Carbon dioxide, carbon tetrachloride, or other chlorinated hydrocarbons. (Also prohibit, water, foam and dry chemical on fires involving these metals - dry sand should be available.) Mercury, chlorine, calcium hypochlorite, iodine, bromine or hydrogen fluoride... [Pg.165]

Picric acid, in common with several other polynitrophenols, is an explosive material in its own right and is usually stored as a water-wet paste. Several dust explosions of dry material have been reported [1]. It forms salts with many metals, some of which (lead, mercury, copper or zinc) are rather sensitive to heat, friction or impact. The salts with ammonia and amines, and the molecular complexes with aromatic hydrocarbons, etc. are, in general, not so sensitive [2], Contact of picric acid with concrete floors may form the friction-sensitive calcium salt [3], Contact of molten picric acid with metallic zinc or lead forms the metal picrates which can detonate the acid. Picrates of lead, iron, zinc, nickel, copper, etc. should be considered dangerously sensitive. Dry picric acid has little effect on these metals at ambient temperature. Picric acid of sufficient purity is of the same order of stability as TNT, and is not considered unduly hazardous in regard to sensitivity [4], Details of handling and disposal procedures have been collected and summarised [5],... [Pg.687]

Interaction of chlorine with methane is explosive at ambient temperature over yellow mercury oxide [1], and mixtures containing above 20 vol% of chlorine are explosive [2], Mixtures of acetylene and chlorine may explode on initiation by sunlight, other UV source, or high temperatures, sometimes very violently [3], Mixtures with ethylene explode on initiation by sunlight, etc., or over mercury, mercury oxide or silver oxide at ambient temperature, or over lead oxide at 100°C [1,4], Interaction with ethane over activated carbon at 350°C has caused explosions, but added carbon dioxide reduces the risk [5], Accidental introduction of gasoline into a cylinder of liquid chlorine caused a slow exothermic reaction which accelerated to detonation. This effect was verified [6], Injection of liquid chlorine into a naphtha-sodium hydroxide mixture (to generate hypochlorite in situ) caused a violent explosion. Several other incidents involving violent reactions of saturated hydrocarbons with chlorine were noted [7],... [Pg.1406]

Prior to 1985, decarboxylation of metal (hydrocarbon) arenedicarboxy-lates was restricted to mercury and to acids with two adjacent carboxylate groups. [Pg.261]

A 5-1. three-necked flask is fitted with a stirrer (which may be of the glass-sleeve type lubricated with paraffin oil, or a mercury-sealed Hirshberg stirrer), an efficient condenser fitted with a calcium chloride drying tube, and a gas inlet tube. The gas inlet tube is connected with polyethylene tubing through a small bubble counter containing a nonvolatile hydrocarbon to the cylinder of boron trichloride. [Pg.147]

A series of alkyl-substituted macrocycles featuring mercury atoms connected by c/-carborane units has been recently synthesized. Examples of such macrocycles include the hexamethyl derivative 58 and the hexadecamethyl derivative 59 whose alkyl-substituted carborane backbones impart improved solubility in hydrocarbon solvents.7 While 58 was synthesized from doso-9, 12-Mc -1 T-I.i -110I R and Hg(OAc)2, compound 59 was obtained as a... [Pg.427]

For this process, suitable solvents include hydrocarbons, benzene, and ether. Lithium alkyls can also be prepared by the reaction of the metal with a mercury alkyl,... [Pg.399]


See other pages where Mercury hydrocarbons is mentioned: [Pg.125]    [Pg.515]    [Pg.281]    [Pg.95]    [Pg.1541]    [Pg.350]    [Pg.147]    [Pg.266]    [Pg.724]    [Pg.348]    [Pg.28]    [Pg.195]    [Pg.139]    [Pg.140]    [Pg.515]    [Pg.26]    [Pg.396]    [Pg.416]    [Pg.458]    [Pg.1035]    [Pg.609]    [Pg.1653]    [Pg.1706]    [Pg.1726]    [Pg.12]    [Pg.496]    [Pg.50]   
See also in sourсe #XX -- [ Pg.21 , Pg.109 ]




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