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Handbook of Solvents - George Wypych - ChemTech - Ventech!

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3.2 Methods <strong>of</strong> solvent manufacture 69<br />

AN =− 59. 9 + 1850 . E T<br />

[3.1.3]<br />

The donor number is frequently used in various fields <strong>of</strong> polymer chemistry (see Chapter<br />

10). Another classification based on acidity/basicity <strong>of</strong> solvents allows the division <strong>of</strong> solvents<br />

into six groups containing protic-neutral; protogenic; protophilic; aprotic-protophilic;<br />

aprotic-protophobic; and aprotic-inert. 4<br />

Snyder 5,6 developed classification <strong>of</strong> solvents for chromatography which arranges solvents<br />

according to their chromatographic strength. It is classification based on the solvent’s<br />

ability to engage in hydrogen bonding or dipole interaction using the experimentally determined<br />

partition coefficients by Rohrschneider. 7 Eight groups <strong>of</strong> solvents were defined<br />

based on cluster analysis. In addition to the usefulness <strong>of</strong> this classification in chromatography,<br />

it was found recently that it is also useful in the design <strong>of</strong> coatings which do not affect<br />

undercoated paints. 8<br />

Numerous other classifications and sets <strong>of</strong> data are available, such as those included in<br />

various databases on solvent toxicity, their environmental fate, combustion properties, explosive<br />

limits, etc.<br />

REFERENCES<br />

1 Ch Reichardt, <strong>Solvents</strong> and <strong>Solvents</strong> Effects in Organic Chemistry, VCH, Weinheim, 1988.<br />

2 V Gutman, G Resch, Lecture Notes on Solution Chemistry, Wold Scientific, Singapore, 1995.<br />

3 G Gritzner, J. Mol. Liq., 73,74, 487-500 (1997).<br />

4 Y Marcus, The Properties <strong>of</strong> <strong>Solvents</strong>, John Wiley & Sons, Chichester, 1999.<br />

5 L R Snyder, J. Chromatographic Sci., 16, 223 (1978).<br />

6 S C Rutan, P W Carr, J Cheong, J H Park, L R Snyder, J. Chromatography, 463, 21 (1989).<br />

7 L Rohrschneider, Anal. Chem., 45, 1241 (1973).<br />

8 I R Owen, US Patent 5,464,888, 3M, 1995.<br />

3.2 OVERVIEW OF METHODS OF SOLVENT MANUFACTURE<br />

<strong>George</strong> <strong>Wypych</strong><br />

ChemTec Laboratories, Inc., Toronto, Canada<br />

Crude oil is the major raw material source for solvents. Aliphatic and aromatic<br />

hydrocarbons are produced by physical processes used in petrochemical industry. Other<br />

solvents are synthetic but their starting raw materials are usually products <strong>of</strong> the petrochemical<br />

industry. Figure 3.2.1 shows the main groups <strong>of</strong> materials produced by petrochemical<br />

industry from crude oil.<br />

Two observations are pertinent: the main goal <strong>of</strong> petrochemical industry is to convert<br />

crude oil to fuels. <strong>Solvents</strong> are only a small fraction <strong>of</strong> materials produced. Figure 3.2.2<br />

shows that solvents are not only used directly as solvents but are also the building blocks in<br />

the manufacture <strong>of</strong> a large number <strong>of</strong> materials produced by organic chemistry plants.<br />

Desalting <strong>of</strong> crude oil is the first step in crude oil processing. It is designed to remove<br />

corrosive salts which may cause catalyst deactivation. After desalting, crude oil is subjected<br />

to atomospheric distillation. Figure 3.2.3 shows a schematic diagram <strong>of</strong> the crude oil distillation<br />

process. The raw material is heated to 400 o C and separated into fractions on 30-50<br />

fraction trays in distillation column. The diagram in Figure 3.2.3 shows the main fractions<br />

obtained from this distillation. The heavier fraction cannot be distilled under atmospheric

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