Wiki: Detergents

A lot of these contain chemicals that produce hydrogen peroxide when used. These often feature 'oxi' in the name. The actual chemical used is often sodium perborate, which is normally mixed with an activator (tetraacetylethylenediamine) to make it effective at lower wash temperatures. Sodium percarbonate is another popular choice.

Regards,

Sid

Reply to
unopened
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Partially the progenitor of the brand name "Persil" (actually from perborate and silicate), I was once told.

Reply to
Appelation Controlee

lye soap has been around longer...

Reply to
The Natural Philosopher

thanks, I've slotted that in.

NT

Reply to
meow2222

The alkali is neither here nor there, but it seems animal fats were the norm in Roman times. Odd that they didn't try olives.

Reply to
Stuart Noble

Too good to waste on washing.

Reply to
The Natural Philosopher

Computing seems so much easier.

Reply to
Huge

Heh, I did a similar thing for central heating oil, using soil scraped from under a leaking CH oil tank as the starter.

I was going to say that at least the subject doesn't die during the test, but then realised that this was not inaccurate.

Reply to
Steve Firth

So how did you extract the excretion products finally? I'd be tempted to remove the water and volatiles by vacuum distillation, then an ether extraction on the condensed volatiles (which shouldn't contain any BBS). Having removed the water, the residue will still have BBS, but without the water, ether extraction should work.

Did you do chromatographic separation of the components afterwards?

Cheers,

Sid

Reply to
unopened

I spent some months many years ago, trying to determine the

I often do that when there's nothing much on the telly.

mark

Reply to
mark

On Wed, 21 Jan 2009 22:03:35 +0000, The Natural Philosopher wrote (in article ):

The Greeks use olive oil soap a lot - it's available everywhere there. I don't suppose they use the best 'Extra Virgin' though - more likely chemically recovered stuff from already used pressings.

Reply to
Mike Lane

I didn't. Summer vacation finished & I went back to being an undergraduate, handing the carboy full of fermenter output and ether back to one of the "proper" research assistants.

That was the intent, yes.

Reply to
Huge

Thought that went to Lidl? (Or was that Aldi?) :-)

Reply to
Rod

Feeling mischievous are we? :-)

Reply to
Stuart Noble

Ahh. I see. I was hoping you'd reposte with a devilishly cunning way of doing it. I would guess at vacuum distillation + condensation of the volatiles. That would leave the BBS behind, and so you'd have an ether extraction of the volatiles ready made. The residue would be water-free, so I'd guess you could then run a standard extraction on it. Chromatographic isolation of the components, followed by photospectometry of each component and confirmation via mass spectrometry. I suspect these days it's all automated.

Cheers,

Sid

Reply to
unopened

Given the last two days, I think I've changed my mind.

Reply to
Huge

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