Re: Cotton wool for lens cleaning

Posted by JOEL B. SHEFFIELD on
URL: http://confocal-microscopy-list.275.s1.nabble.com/Cotton-wool-for-lens-cleaning-tp6175236p6178273.html

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Colleagues,

I would like to report on a discovery that we have made concerning lens
cleaning.  In our teaching labs,  we have a particularly difficult problem
with 40x dry lenses that are routinely dipped into oil by inexperienced
students.  These lenses have a small meniscus front lens element that is
very difficult to clean with the conventional methods listed so far.
Recently, during a trip to a supermarket, I came across microfiber cleaning
cloths designed for glass cleaning that are 80% Polyester and 20% Nylon.
The surface of the cloths is tufted, with a fine pile that enters the
meniscus and It turns out that the combination of fibers sucks up oil
without the need for any other solvents, leaving the lenses remarkably
clean.

In the past, we have had to remove the lenses to clean them.  Now, we can
leave them on the scope and essentially wipe them clean.

Joel


On Wed, Mar 16, 2011 at 11:12 AM, Daniel James White <[hidden email]>wrote:

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> On Mar 16, 2011, at 6:16 AM, CONFOCALMICROSCOPY automatic digest system
> wrote:
>
> >
> > Date:    Tue, 15 Mar 2011 15:03:31 -0400
> > From:    "Aleksandrs Spurmanis, Mr." <[hidden email]>
> > Subject: Cotton wool for lens cleaning
> >
> > *****
> > To join, leave or search the confocal microscopy listserv, go to:
> > http://lists.umn.edu/cgi-bin/wa?A0=3Dconfocalmicroscopy
> > *****
> >
> > Dear list,
> >
> > The current practice at our facility is to inspect and clean the
>  objective=
> > s of our scopes periodically (approx. once every 2-3 months for each
> scope)=
> > using lens paper wrapped around small clean-room swabs.  I had noticed,
> ho=
> > wever, that the field service technicians who run the PMs on our
> instrument=
> > s tend to use 100% cotton wool (which I understand to be essentially the
> sa=
> > me material as your basic 100% cotton ball in the pharmacy) and are able
> to=
> > service our lenses in a much more efficient manner (read: waayyy quicker)
> =
> > than myself using my current methods.  In the interests of improving my
> mai=
> > ntenance efficiency, I've been considering trying this out myself but
> wante=
> > d to check in with the list to see if anyone can share their experiences,
> i=
> > nsights or advice before proceeding.  My main concern is that the cotton
> mi=
> > ght contribute to premature wear on the lens coating.  As cleaning
> solvents=
> > , I use either Glass Plus, anhydrous ethanol and/or water.
>
> Here is what we do...
>
> https://ifn.mpi-cbg.de/wiki/ifn/index.php/Clean_objective_lens
>
> Zeiss and API both use clean cotton wool wrapped onto a wooden stick,
> self made or commercial versions.
>
> If you use these, then only roll the cotton wool over the glass surface -
> NO SCRUBBING or other aggressive scraping or gouging.
> Finish off the cleaning using a quality lens cleaning tissue paper - never
> a kim wipe etc.  (contains particles of hard minerals)
> with 70& ethanol or 4:1 Ether:Ethanol.
>
> Some like to use chloroform... but we can't use it outside a fume hood, so
> its not an option.
>
> For Water dipping lenses that go into PBS or other buffers use a tris pH8
> buffered 0.5 M EDTA / EGTA solution to dissolve Ca-phosophate residues
> BEFORE you use a cotton bud or tissue.
>
> I find that using a stereo microscope with a ring light around the stereo
> scope's objective
> is the only way to really see of the glass surface of the lens is clean.
>
> You have to look at it with some magnification with angled illumination to
> see the dirt.
>
> cheers
>
> Dan
>
>
>
>
> >
> > Thanks in advance.
> >
> > Sincerely,
> >
> > Aleksandrs J. Spurmanis
> > Microscopy Specialist
> > Imaging Facility
> > McGill University Life Sciences Complex
> > Francesco Bellini Building
> > 3649 Sir William Osler
> > Suite 137
> > Montreal, QC
> > H3G 0B1
> > tel.:  (514)-398-5248
> > fax:  (514)-398-7452
> > [hidden email]
> > http://www.mcgill.ca/lifesciencescomplex/core/imaging/
>
> Dr. Daniel James White BSc. (Hons.) PhD
> Senior Microscopist / Image Visualisation, Processing and Analysis
> Light Microscopy and Image Processing Facilities
> Max Planck Institute of Molecular Cell Biology and Genetics
> Pfotenhauerstrasse 108
> 01307 DRESDEN
> Germany
>
> +49 (0)15114966933 (German Mobile)
> +49 (0)351 210 2627 (Work phone at MPI-CBG)
> +49 (0)351 210 1078 (Fax MPI-CBG LMF)
>
> http://www.bioimagexd.net       BioImageXD
> http://pacific.mpi-cbg.de               Fiji -  is just ImageJ (Batteries
> Included)
> http://www.chalkie.org.uk               Dan's Homepages
> https://ifn.mpi-cbg.de                  Dresden Imaging Facility Network
> dan (at) chalkie.org.uk
> ( white (at) mpi-cbg.de )
>



--


Joel B. Sheffield, Ph.D
Department of Biology
Temple University
Philadelphia, PA 19122
Voice: 215 204 8839
e-mail: [hidden email]
URL:  http://astro.temple.edu/~jbs