Page 7 - June 2024 Newsletter
P. 7

Fortunately, Campbell—who had trained as a scientist himself—
         loved the joke, and printed Asimov’s spoof in the March 1948
         issue.
            In actual fact, it’s really quite a weak joke. If it had been written
         up in the form of an ordinary short story, it would have been a
         forgettable one. The idea is simply that a fictitious substance
         called “thiotimoline” dissolves in water a second or so before it’s
         actually added. What makes the six-page piece so memorable—
         and genuinely very funny—is its ostensibly serious format,
         complete with numerical tables, diagrams and a formal list of
         references at the end. All these things are absolutely standard in
         scientific papers, but they’d never been seen before in a work of
         fiction.
            The thiotimoline piece highlighted a strange-but-true fact about
         spoofs in general: no matter how outrageous they are, if they’re
         written in a superficially factual style, some people will take them
         for the truth.
            Here is the opening of “The Endochronic Properties of
         Resublimated Thiotimoline”, which gives a good flavour of its
         deliberately turgid style:
            It has been long known that the solubility of organic
         compounds in polar solvents such as water is enhanced by the
         presence upon the hydrocarbon nucleus of hydrophilic—i.e. water
         -loving—groups, such as the hydroxy (–OH), amino (–NH2), or
         sulphonic acid (SO3H) groups. Where the physical characteristics
         of two given compounds—particularly the degree of subdivision of
         the material—are equal, then the time of solution—expressed in
         seconds per gram of material per millilitre of solvent—decreases
         with the number of hydrophilic groups present. Catechol, for
         instance, with two hydroxy groups on the benzene nucleus
         dissolves considerably more quickly than does phenol with only
         one hydroxy group on the nucleus. Feinschreiber and Hravlek  in
                                                                       2
         their studies on the problem have contended that with increasing
         hydrophilism, the time of solution approaches zero.
            That this analysis is not entirely correct was shown when it was


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