You are on page 1of 1

Three-in-one: VMA 600 Ex CIP

The granulation process is automated/


plc-controlled. The product-specific re-
cipes are simply loaded from a PC and

single pot granulator


the required process functions can be
set via HMI:

FEEDING:
The raw powder is fed by vacuum first,
e.g. from an IBC container.

BLENDING:
The powder is blended through the
main impeller for a few minutes.

Detailed view of the VMA process bowl lid.


GRANULATION:
The binding agent is added to the pro- DISCHARGING: The required cooling water is held stea-
duct from a stirred liquid tank via mass The process bowl can be easily dischar- dy at -30 °C or -20 °C or +5 °C in a
flow sensor and peristaltic pump to an ged through the center discharge valve chiller unit (see picture).
atomizing spray nozzle. At the same via an inline conical turbo sieve (Bohle
time, the impeller and chopper provide Turbo Sieve BTS 200) into an IBC con- The emission rate of e.g. acetone or
the necessary shear forces to generate tainer. ethanol can be set to below 20 % LEL
granules. (lower explosion limit).

CLEANING: Bohle is presenting the latest genera-


WET MIXING: Before processing another product, the tion of the VMA 300 at the ACHEMA
If required, a short wet mixing phase unit should be cleaned. trade fair in Frankfurt.
can be integrated into the process after
adding the liquid to bring the granules The cleaning process of the VMA is The “compact all-rounder” is offered
In December 2014, the VMA 600 was dispatched from Plant 3. Batches of up to 480 litres can be produced. to the final size and shape. automated, recipe-controlled and very at capacities between VMA 70 to VMA
quick. A CIP rack in the technical area 1200 which corresponds to batch sizes
For decades, high shear single pot gra- The single pot granulator offers many ad- The Bohle VMA series includes typical provides the cleaning water at the re- of 20 – 960 litres.
nulation has been a well-established vantages for pharmaceutical companies: pharmaceutical single pot granulators VACUUM DRYING: quired temperature, amount and deter-
process technology within the phar- with impeller and chopper unit and top Three different vacuum processes are gent concentration.
maceutical industry. This process com- ¾¾Safe production in a closed con- drive for pharmaceutical applications. available for drying the granules down
bines three process steps in one pot tainer under vacuum Two agitators provide the necessary to the desired moisture content: When drying is performed, the evapo-
¾¾High blending and granulation shear forces and de-lumping to achieve rated solvents are discharged from the
1. blending, efficiency, even with low dosage high-quality granulates. 1. pure vacuum drying, process bowl to the vacuum system.
2. high shear wet-granulation and API (<1 %) 2. vacuum drying with strip gas
3. drying (under vacuum, gas stripping ¾¾Low drying temperatures under The heart of the machine is the GMP- (VAGAS®) or For environmental reasons, the organic
and/or microwave heat). vacuum, especially suited for compliant double jacket process bowl. 3. 
 with vacuum microwave drying. solvent vapors containing e.g. acetone
temperature-sensitive products The main aggregates are integrated in The organic solvent vapors are con- or ethanol are easily and very efficiently
¾¾Small product contact surface for the lid of the pot (“top drive”). It con- densed and can be recovered or di- condensed in tube condensers.
quick and easy cleaning and fast tains the impeller shaft and sealing, the scharged in an especially effective
product change-over chopper shaft and sealing, the product and environmentally safe way.
¾¾Efficient solvent recovery through filter, the microwave window, the tem-
cooling water perature and pressure sensors as well
¾¾Small footprint as the retractable cleaning nozzles.

You might also like