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CS2

Tail gas containing traces of SO2, H2S, COS and CS2 are usually sent to a finishing processing before being incinerated. [Pg.405]

The effect of temperature on contact angle is seldom very great, as a practical observation. Some values of d0/dTare included in Table X-2 a common figure is about -0.1 degrees/K (but note the case of CS2 on ice also rather large temperature changes may occur in L1-L2-S systems (see Ref. 160). [Pg.369]

From stochastic molecnlar dynamics calcnlations on the same system, in the viscosity regime covered by the experiment, it appears that intra- and intennolecnlar energy flow occur on comparable time scales, which leads to the conclnsion that cyclohexane isomerization in liquid CS2 is an activated process [99]. Classical molecnlar dynamics calcnlations [104] also reprodnce the observed non-monotonic viscosity dependence of ic. Furthennore, they also yield a solvent contribntion to the free energy of activation for tlie isomerization reaction which in liquid CS, increases by abont 0.4 kJ moC when the solvent density is increased from 1.3 to 1.5 g cm T Tims the molecnlar dynamics calcnlations support the conclnsion that the high-pressure limit of this unimolecular reaction is not attained in liquid solntion at ambient pressure. It has to be remembered, though, that the analysis of the measnred isomerization rates depends critically on the estimated valne of... [Pg.860]

Tokmakoff A and Fleming G R 1997 Two-dimensional Raman spectroscopy of the intermolecular modes of liquid CS2 J. Chem. Phys. 106 2569-82... [Pg.2001]

Tokmakoff A, Lang M J, Jordanides X J and Fleming G R 1998 The intermolecular interaction mechanisms in liquid CS2 at 295 and 165 K probed with two-dimensional Raman spectroscopy Chem. Phys. 233 231-42... [Pg.2001]

The CS2 is then removed, after cooling, by a solvent. The molecule has a covalent linear structure S==C=S. [Pg.201]

Without carbon, the basis for life would be impossible. While it has been thought that silicon might take the place of carbon in forming a host of similar compounds, it is now not possible to form stable compounds with very long chains of silicon atoms. The atmosphere of Mars contains 96.2% CO2. Some of the most important compounds of carbon are carbon dioxide (CO2), carbon monoxide (CO), carbon disulfide (CS2), chloroform (CHCb), carbon tetrachloride (CCk), methane (CHr), ethylene (C2H4), acetylene (C2H2), benzene (CeHe), acetic acid (CHsCOOH), and their derivatives. [Pg.16]

Note 1. Prepared by adding CS2 to CH MgBr in THE at 0°C, preferably in the presence of a small amount of CuBr (2 mol %), and subsequently alkylating with ethyl iodide . [Pg.202]

An SO species is generated by the reaction of SO2 with CS2 in the presence of a Pd catalyst and reacts with butadiene to afford the I, 4-disulfoxide Ill[l04],... [Pg.440]

In 1891, Miolati (75) confirmed the cyclic formula of Liebermann and Lange by preparing the compound by three new pathways (1) reaction of CS2 on thiohydantoin, (2) condensation of ammonium dithiocarbamate with chloroacetic ester, (3) reaction of HjS on thiocyanoacetic acid. [Pg.19]

In 1882, Will (90), by reacting CS2 with the product (56) resulting from the condensation of dibromoethane with N,N -diphenylthiourea, obtained the first derivative of thiazolidine-2-thione (57). He observed the reaction of 57 with methyl iodide to afford an addition compound (58). [Pg.21]

In 1890, Gabriel and Lauer (92) established that a-bromoamines react with CS2 to give 2-mercaptothiazolines (61). In the same laboratory, Hirsch (93) reacted /x-mercapto -methylthiazoline (61) with various alkyl iodides and obtained the corresponding S-alkyl derivatives. [Pg.21]


See other pages where CS2 is mentioned: [Pg.145]    [Pg.32]    [Pg.48]    [Pg.81]    [Pg.81]    [Pg.82]    [Pg.144]    [Pg.145]    [Pg.217]    [Pg.377]    [Pg.394]    [Pg.394]    [Pg.407]    [Pg.105]    [Pg.106]    [Pg.366]    [Pg.859]    [Pg.1989]    [Pg.196]    [Pg.396]    [Pg.54]    [Pg.224]    [Pg.440]    [Pg.440]    [Pg.60]    [Pg.225]    [Pg.225]    [Pg.229]    [Pg.229]    [Pg.229]    [Pg.231]    [Pg.232]    [Pg.236]    [Pg.236]    [Pg.241]    [Pg.245]    [Pg.252]    [Pg.252]   
See also in sourсe #XX -- [ Pg.3 , Pg.252 ]

See also in sourсe #XX -- [ Pg.582 ]




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CS2 CARBON DISULFIDE

CS2, inside

CS2, reactions

General procedure for the preparation of dithioesters from CS2 and Grignard reagents

Recovery of CS2 through adsorption on activated carbon

Recovery of CS2 through condensation

Sulfides (H2S, CS2, COS, RSH) Reduced sulfur

With SO2, CS2, and

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