Vacuum Conveying In The Pharmaceutical Industry - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Vacuum Conveying In The Pharmaceutical Industry


Pharmaceutical Technology Europe
Volume 22, Issue 8


Sharon Nowak
Pneumatic conveying via vacuum has been used in the pharmaceutical industry for some time now. What are the newest trends in conveying of pharmaceutical powders and blends?

It is true that powder transfer via vacuum has been in use in the pharmaceutical industry for many years. Obviously, vacuum, (usually via dilute phase) has been the transfer mode of choice because of its inherent ability to keep the powder contained within the system due to the suction created by the vacuum. This is in contrast to positive pressure conveying, which is often used in other industries for high volume and long distances. Positive pressure systems have the disadvantage of possible outward leakage, particularly in cases of improperly aligned or incorrectly installed pipework.

Newer trends in conveying involve dense phase vacuum transfer for pre-blends and granulations, specialty designs for containment and cleaning, and the increased use of specially designed pneumatic receivers for refill operations for continuous pharmaceutical processes, such as continuous granulation, mixing/blending, and extrusion.

What are the differences between dense phase and dilute phase conveying?


Figure 1
Dilute phase conveying is typically used with materials where segregation or attrition in the conveying line is not a concern. Comparative gas/air velocities in a 3 inch pipe for dilute phase can range from 15.2 up to 35.6 m/sec (3000 to 7000 ft/min). In dense phase operations (Figure 1), a reduced gas velocity range of 0.4 to 8.6 m/sec (80 to 1700 ft/min) is utilised. In most applications the gas is air, however, in the pharmaceutical industry nitrogen is also widely used because of its inert nature, as well as the natural purity of the gas.

By definition, dense phase means a higher product to gas ratio, in other words a smaller amount of gas is used to move a larger quantity of product. The less gas required for transfer, the lower the power consumption of the exhauster or vacuum pump. Typically material is picked up from the outlet of a specialty hopper, which minimises the amount of air entrained in the material, and allows the slugs of product to form. In addition, the hopper also includes a type of make-up air inlet, which aids in forming the slugs as the material enters the conveying line. The combination of a relatively low air velocity and an expanded line size result in a "siphon-like" effect, transporting the material to the vacuum receiver.

The lower gas velocity used in dense phase conveying results in a much gentler action, reducing wear on the conveyed powder or granulate. This gentle action also reduces the segregation issues often experienced with the more aggressive dilute phase operation, making it ideal for the conveying of powder blends to tabletting machines or roller compactors. It should be noted, however, that there are limitations to the application of dense phase vacuum conveying; for example, conveying distances may not exceed 3.7 m (12 ft) vertical and 4.6 m (15 ft) horizontal. Also, dense phase conveying is not appropriate for conveying materials that are cohesive, hygroscopic or so coarse in particle size that they will not readily form slugs. While dilute phase vacuum conveying is fairly forgiving, dense phase is very dependent on the material characteristics; therefore it is highly advisable to perform full-scale tests when modeling a dense phase vacuum system.


ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
70%
Breakthrough designations
4%
Protecting the supply chain
17%
Expedited reviews of drug submissions
2%
More stakeholder involvement
7%
View Results
Eric Langerr Outsourcing Outlook Eric LangerTargeting Different Off-Shore Destinations
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAsymmetric Synthesis Continues to Advance
Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
New FDA Team to Spur Modern Drug Manufacturing
From Generics to Supergenerics
CMOs and the Track-and-Trace Race: Are You Engaged Yet?
Ebola Outbreak Raises Ethical Issues
Better Comms Means a Fitter Future for Pharma, Part 2: Realizing the Benefits of Unified Communications
Source: Pharmaceutical Technology Europe,
Click here