CryoNet #33255
CryoNet <[email protected]> 20 Jan 2011 10:00:01 -0000
| Newsgroups | gmane.culture.science.cryogenics |
|---|---|
| Message-ID | <[email protected]> |
CryoNet - Thu 20 Jan 2011
#33255: Automated Data Collection [M2darwin]
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Message #33255
From: [email protected]
Date: Wed, 19 Jan 2011 06:49:14 EST
Subject: Automated Data Collection
In a message dated 1/19/2011 2:00:07 A.M. Pacific Standard Time,
[email protected] writes:
Mike Darwin writes:
> MD: I'll leave this question to Brian, because he can discourse at
> length on the magic that is differential scanning calorimetery
> (DSC). DSC can detect the minutest of phase changes in a sample,
> and if your numbers all sum out right, then you can be pretty sure
> "what's what" after cooling to any given temperature. I was still
> at 21CM when Brian began this work, and it was horrible - the kind
> of thing that would drive me barking mad. Basically you crimp a
> tiny volume of solution 'just so' into sealed metal pans, and put
> them in the device and cool them. Of course, the catch is, that
> you must do this thousands and thousands of times to build a
> picture of how different solutions behave under different regimens
> of cooling and re-warming. It is boring, repetitive and truly
> dull work.>>
These days, this is what one builds small robots to do. (That is what
has made much of recent science possible. No one could handle the
precision and boredom associated with many modern data collection
tasks -- automation is why they are possible at all. Luckily,
technology to do things like that has gotten dirt cheap in the last
decade or so.)
Perry,
I'm often surprised by what is automated and what is not.
I love to visit factories of all kinds everywhere I go (hospitals too),
and I see that my interest must be shared by others, because there are now
these (to me at least) absolutely captivating TV programmes like "How It's
Made." In Chen Chang, I saw all kinds of factories, and I observed a lot of
automation, but only where cleanliness, rapidity and high precision were
required. Where people can do, they are still used. By contrast, in Germany,
the UK and the US, even very basic tasks that are not very sophisticated are
automated. The difference is the cost of labor (and the regulatory burden).
As it turns out, it costs a tremendous amount of money to automate any
kind of precision, multi-step process.
A machine to manufacture needles may cost upwards of a million dollars. Of
course, that's a bargain compared to paying the people required (in a
developed country) to do the job. Aside from the high direct costs, people are
a pain the arse. And even then, costs are as low as they are because a lot
of manufacturing automation will not be a 'one-off' - other people need
needle making machines, too.
Preparing the sample for analysis in the DSC requires (at least) these
steps:
1) Someone has to mix up the various solutions that are to be evaluated.
These solutions will 'one-offs' that are made up just for the purpose of
evaluation. It's not like you are taking samples from various batches of
medicine, soda, beer, etc., that being produced en masse for commerce.
2) The DSC 'pans' are very small, indeed tiny little metal containers -
smaller than most hearing aid batteries. They must be filled with care and
precision: no air bubbles can be present, and care must be taken to avoid
contamination of the sample with water from the atmosphere in the case of
hygroscopic CPAs (i.e., most of them).
3) The pan must be very artfully closed and crimped, and only then is it
place in the DSC.
The whole thing is a nightmare of careful and precise labor. And of
course, you can't mix up 1 mL of your putative CPA mixtures, because you can't
measure that precisely or repeatedly. [Actually, you can, but
microchesmistry has its own headaches and is only economical if the reagents cost a
fiortune.]
Could a machine do all this? Absolutely! Just be prepared to shell out
$1-2 million and to spend a couple of years ironing out the bugs. AND you will
have a lot of overhead in the form of skilled people to maintain the
machine. Turn out, wasting a brilliant mind like Brian Wowk's on such dreary
business is cost effective. Also, there are technicians who can be trained to
do this work.
The brutal fact is that this civilization does not much value intellects
such as Brian's. Nor do they value any intellect that does not provide a
return on investment within ~5 years, on average.
As someone who has had direct experience trying to automate some
comparatively simple things, such as cardiopulmonary bypass (CPB) (which is very
simple to automated compared to some of the unbelievably complex and exactly
manufacturing processes I've seen automated), it can be surprisingly
difficult, even if you have you have experts, and enormous computing power at your
disposal. CPB is arguably no more complex than flying and landing a
jetliner - and that process has been fully automated for at least a decade. Yes,
you still need a pilot, and you would still need a perfusionist in
automated CPB, but such automation provides enormous added safety (used wisely) and
it also may allow for the use of knowledgeable, but less skilled
personnel, in emergent situations - such as in-field CPB for refractory cardiac
arrest. [You can have knowledge without reflexes!]
However, such automation is challenging, and even if achieved, there has
to be a market for it. Due mostly to regulatory constraints, that market is
not there for automated CPB. That means you have no economies of scale and
that further drives up the price and drives down the reliability of any
system you do develop. Wide use = robustness and reliability. As to automating
CPA evaluation, well, that is so far from a priority for this civilization
it is impossible to put into words. At least not words I can post here
;-0.
Mike Darwin
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