What bewilders me is the concept of a College being a drug free zone! I have been reading a very old book on photographing the invisible, and clearly what you have here is ectoplasm.
Tony
Tony
Was it a "Voila!" or a "LOOK OUT!" type of light?
Could be Liberty University in Lynchburg... different opiate according to Marx.What bewilders me is the concept of a College being a drug free zone!

I blame the liberal media! They're obviously trying to ignite some chemical scare, and we all know hippies like the colour green.
Actually I guess I already spoiled it when I mentioned chemiluminescence. Indeed an excited state intermediate is forming in the developer, and when that alkali hits the stop (which is big pH swing), *flash* the excited state is quenched. It's not too suprising that a ring-based compound, such as found in the pyrocatechol-based developers, acts this way. What is surprising to me is that this can be seen so readily and without a more oxidative quench treatment such as from peroxide or such. Anyway there has to be a reason why it's called pyro, right?!Neither are the all non-tenured teaching staff at Liberty University.lol
Lee, I am not at Liberty!
The name Liberty University is an oxymoron.An exothermic reaction may also release energy in other
forms of energy apart from heat. Reactions that release energy
greater than 41 kcal per mole can give CL-emission. Oxidation
reactions are usually accompanied by large energy release.
The wavelength of CL-emission is calculated from the equation
E = hc/λ, (1)
where h = Planck constant, c = the velocity of light, and λ =
the wavelength of the emitted light.
lol
Railwayman, you went and spoiled the mystery!![]()

Ole mentioned polymerization giving the brownish colour of the developer as it ages, which is an aspect I hadn't thought of.
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