24585
Accession Number
20333
Author
Williams, Donald C.
Title Of Article Chaper
Solvents and Solutions or What is lacquer thinner, and why does it do what it does to varnish?
Title Of Journal Book
The Wood Finisher
Issue
4
Pages
44324
Collation
4 p. : ill., 1 fig.
Language Of Text
English
Literature Type
Serial
Literature Level
Analytic
Abstract
To provide a framework for discussing why different solvents act the way they do, generalized molecular structures of two important solvent families used in lacquer thinners are described. The hydrocarbon family is made up of three main groups - aliphatic, aromatic and chlorinated hydrocarbons. Saturated aliphatic hydrocarbons have groups of molecules that have only C-C single bonds and no C=C double bonds. Examples such as hexane, heptane and octane are components of oil based reactive finishes such as polyurethanes. The cyclic aliphatic hydrocarbons are saturated hydrocarbons that have formed a ring or multiple ring structure. Cyclohexane and turpentine are examples. Aromatic hydrocarbons such as toluene, ethyl, xylene and diethylbenzene are based on the benzene molecule and are important components of some acrylic and nitrocellulose lacquers. Chlorinated hydrocarbons include methylene chloride which is the main ingredient in most solvent-type paint removers. They have one or more hydrogen atoms replaced by an atom from the halogen group. The second family of solvents, the oxygenated solvents, incorporates oxygen atoms into the hydrocarbon structure. This family includes esters, glycol ethers, ketones, and alcohols. Important solvent chemicals in these groups are ethyl acetate, methyl cellosolve , acetone, and methanol respectively. This is part 1 of a two part article on solvents and solutions.
Keywords
varnish;solvents;alkane;paraffin;alkyd;petroleum ether; naphtha; petroleum benzine;volatility;Stoddard solvent;paint thinner; terpenes;butyl cellosolve;methyl ethyl ketone;synthetic resin; shellac;ethanol
pub_id
24585