Creative Chemistry - Descriptive of Recent Achievements in the Chemical Industries by Edwin E. Slosson
page 133 of 299 (44%)
page 133 of 299 (44%)
![]() | ![]() |
|
|
loss of months of labor. The reason the chemist did not do anything
further with the gummy stuff that stuck up his test tube was because he did not know what to do with it. It could not be dissolved, it could not be crystallized, it could not be distilled, therefore it could not be purified, analyzed and identified. What had happened was in most cases this. The molecule of the compound that the chemist was trying to make had combined with others of its kind to form a molecule too big to be managed by such means. Financiers call the process a "merger." Chemists call it "polymerization." The resin was a molecular trust, indissoluble, uncontrollable and contaminating everything it touched. But chemists--like governments--have learned wisdom in recent years. They have not yet discovered in all cases how to undo the process of polymerization, or, if you prefer the financial phrase, how to unscramble the eggs. But they have found that these molecular mergers are very useful things in their way. For instance there is a liquid known as isoprene (C_{5}H_{8}). This on heating or standing turns into a gum, that is nothing less than rubber, which is some multiple of C_{5}H_{8}. For another instance there is formaldehyde, an acrid smelling gas, used as a disinfectant. This has the simplest possible formula for a carbohydrate, CH_{2}O. But in the leaf of a plant this molecule multiplies itself by six and turns into a sweet solid glucose (C_{6}H_{12}O_{6}), or with the loss of water into starch (C_{6}H_{10}O_{5}) or cellulose (C_{6}H_{10}O_{5}). But formaldehyde is so insatiate that it not only combines with itself |
|


