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CILAS laser - the automated auto sampler

 

Key Features

 

 

 

 

 

 

 

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WET AND DRY DISPERSION

Cilas' patented design provides customers with an integrated wet and dry dispersion system. The transition from wet to dry dispersion modes is accomplished via software with one click of the mouse. Our unique design eliminates the need for the operator to swap hardware when switching modes.  This also eliminates the need to realign and revalidate the analyzer when switching between dispersion modes.

All Cilas systems can be configured for wet dispersion, dry dispersion or wet and dry dispersion, based on customer need.

 

Companies manufacture a wide range of particles.  When they want to analyze particle size, there are two available techniques, wet dispersion or dry dispersion.  Ideally the best choice for particle size measurement is wet dispersion.  This mode allows the user to select internal ultrasonics, stirring or the pump to break up any agglomerates.  Water, alcohol  or other solvents can be used in wet dispersion mode.

If a particle is soluble in water or reacts with water, customers can choose to run the sample in dry dispersion.  This avoids using water or any other solvent.  Other samples that might not distribute well in a solvent are best run in dry mode.  Using Cilas' new dry jet dispersion technique, the pressure required to disperse powders is low, which means deagglomeration can be achieved without breaking particles.

Cilas application specialists can help our users decide whether wet or dry dispersion is best for their samples. 


Come and see our solutions at the following trade shows:

 

International Conference & Exhibition on Advanced Ceramics & Composites

Booth 223

Daytona Beach, FL

January 29 - 30, 2008

 

Pittcon 2008

Booth 1960

New Orleans, LA

March 1 - 7, 2008

 

Particle Society of Minnesota

Roseville, MN

March 19, 2008

 

International Powder & Bulk Solids Show

Booth 2655

Chicago, IL

May 5 - 8, 2008

 

American Coatings Show 2008

Booth 929

Charlotte, NC

June 3 - 5, 2008

 

MS&T 2008

Pittsburg, PA
October 5 - 8, 2008

 

American Association of Pharmaceutical Scientists 2008

Booth 240

Atlanta, GA

November 16 - 20, 2008

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