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Hydrocarbon across water

When we consider the interaction of a hydrocarbon with itself across a vacuum, em = evacuum = 1, the magnitude of the force and the spectrum of contributions look very different. The n = 0 term comes out to 0.5(2.04 — 1 /2.04 + l)2 = 0.059. The nine IR terms sum to 1.031 followed by the visible-frequency terms that sum to 1.162, and finally a very strong 5.449 from the UV. The total summation comes to approximately 7.7, compared with 0.63 of the same hydrocarbon across water. [Pg.63]

How does the interaction of hydrocarbon across water change when a solute is added to solvent water ... [Pg.70]

Gustafson, K.E., and Dickhut, R.M. (1997a) Gaseous exchange of polycyclic aromatic hydrocarbons across the air-water interface of southern Chesapeake Bay. Environ. Sci. Technol. 31, 1623-1629. [Pg.590]

To see how these different e(i ) functions combine to create an interaction, consider the case of two hydrocarbon half-spaces A = B = H across water medium m = W. First plot eH(/ ) and ew(i ) as continuous functions [see Fig. LI.22(a)]. These are plotted at only the discrete sampling frequencies at which they are to be evaluated a log plot in frequency shows how compression of the arithmetically even spacing fit- = 0.159 n eV in index n works with the varying difference in eH(/ ) and ew(i ) [see Fig. LI. 22(b)],... [Pg.61]

Fig. 5. Force measured in water between LB films of DODAB deposited on mica. Data plotted in open symbols. The different symbols denote separate series of measurements. Forces measured in water (pH = 5.6) between mica surfaces coated with polymerised monolayers of OTE (different filled symbols represent separate series of measurement). The solid lines show the van der Waals forces expected between mica surfaces (1) and hydrocarbon surfaces (2) across water. Redrawn with permission from Ref. [92]. 1995, VPS. Publishers and Brill Academic Publishers. Fig. 5. Force measured in water between LB films of DODAB deposited on mica. Data plotted in open symbols. The different symbols denote separate series of measurements. Forces measured in water (pH = 5.6) between mica surfaces coated with polymerised monolayers of OTE (different filled symbols represent separate series of measurement). The solid lines show the van der Waals forces expected between mica surfaces (1) and hydrocarbon surfaces (2) across water. Redrawn with permission from Ref. [92]. 1995, VPS. Publishers and Brill Academic Publishers.
The DME reactor effluent is split into four parallel streams, mixed with heated recycle gas and passed into four parallel conversion reactors containing ZSM-5 catalyst, where the conversion to hydrocarbons and water is completed and the remaining heat of reaction released. Recycle gas is used to limit the temperature rise across the reactors. [Pg.697]

Ogura I, Masunaga S, Nakanishi J (2001) Parameters characterizing atmospheric behavior of PCDDs/PCDFs. Organohalogen Compd 52 483-486 Pandit GG, Sahu SK, Puranik VD, Venkat Raj V (2006) Exchange of polycyclic aromatic hydrocarbons across the air-water interface at the creek adjoining Mumbai harbour. India Environ Int 32 259-264... [Pg.305]

Water sampling with a spiral hollow polydimethylsiloxane (PDMS) membrane was used with IMS for in situ sampling and analysis of trace chlorinated hydrocarbons in water in a single procedure. Aqueous contaminants permeate across the membrane into a gas flow, through the membrane tube, and into a specially made... [Pg.356]

Fig. 4 Intermolecular forces vs. distance between a sphere (with a radius of 50 nm) and flat surfaces. Solid curve both sphere and planar surface are terminated by hydrocarbon groups across water as a medium, with a Hamaker constant of 4.5 x 10 J ([113], pg 189). Dashed curve both sphere and planar surface are modified with bUayer surfaces composed of the uncharged sugar-headgroup lipid, monogalactosyl diglyceride in 0.15 M NaCl, with a Hamaker constant of 3.5 x 10 J ([113], pg 396) (source Zou S., private communication)... Fig. 4 Intermolecular forces vs. distance between a sphere (with a radius of 50 nm) and flat surfaces. Solid curve both sphere and planar surface are terminated by hydrocarbon groups across water as a medium, with a Hamaker constant of 4.5 x 10 J ([113], pg 189). Dashed curve both sphere and planar surface are modified with bUayer surfaces composed of the uncharged sugar-headgroup lipid, monogalactosyl diglyceride in 0.15 M NaCl, with a Hamaker constant of 3.5 x 10 J ([113], pg 396) (source Zou S., private communication)...
In order to include other interactions such as dipolar or hydrogen bonding, many semiempirical approaches have been tried [196, 197, 200], including adding terms to Eq. X-45 [198, 201] or modifying the definition of [202, 199]. Perhaps the most well-known of these approaches comes from Fowkes [203, 204] suggestion that the interactions across a water-hydrocarbon interface are dominated by dispersion forces such that Eq. X-45 could be modified as... [Pg.376]

Cyclodienes. These are polychlorinated cycHc hydrocarbons with endomethylene-bridged stmctures, prepared by the Diels-Alder diene reaction. The development of these insecticides resulted from the discovery in 1945 of chlordane, the chlorinated adduct of hexachlorocyclopentadiene and cyclopentadiene (qv). The addition of two Cl atoms across the double bond of the ftve-membered ring forms the two isomers of chlordane [12789-03-6] or l,2,4,5,6,7,8,8-octachloro-2,3,3t ,4,7,7t -hexahydro-4,7-methano-lJT-indene, QL-trans (mp 106.5°C) and pt-tis (32) (mp 104.5°C). The p-isomerhas signiftcantiy greater insecticidal activity. Technical chlordane is an amber Hquid (bp 175°C/267 Pa, vp 1.3 mPa at 25°C) which is soluble in water to about 9 fig/L. It has rat LD qS of 335, 430 (oral) and 840, 690 (dermal) mg/kg. Technical chlordane contains about 60% of the isomers and 10—20% of heptachlor. It has been used extensively as a soil insecticide for termite control and as a household insecticide. [Pg.277]

Perhaps the most important experimental progress made recently in electrochemistry was the introduction of a scanning electrochemical microscope (SECM). Tsionsky et al. have used SECM to study also the rate of ET across a lipid monolayer at the water-benzene interface [48,49]. The presence of the monolayer decreased the rate of ET, being the decrease more significant for longer hydrocarbon chains and larger lipid concentration in solution. It was thus concluded that the ET reaction does not occur at defect sites in the lipid monolayer. [Pg.544]

The water can be assumed to be dispersed in the hydrocarbon. Estimate the size of decanter required to separate the mixture in a horizontal drum with a length to diameter ratio of 3 to 1 and an interface across the center of the drum. [Pg.147]


See other pages where Hydrocarbon across water is mentioned: [Pg.64]    [Pg.64]    [Pg.71]    [Pg.64]    [Pg.64]    [Pg.71]    [Pg.931]    [Pg.376]    [Pg.168]    [Pg.316]    [Pg.303]    [Pg.931]    [Pg.304]    [Pg.46]    [Pg.232]    [Pg.132]    [Pg.2592]    [Pg.328]    [Pg.475]    [Pg.275]    [Pg.630]    [Pg.263]    [Pg.63]    [Pg.63]    [Pg.375]    [Pg.819]    [Pg.238]    [Pg.101]    [Pg.43]    [Pg.44]    [Pg.94]    [Pg.417]    [Pg.53]    [Pg.558]    [Pg.872]   


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Hydrocarbon water

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