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Talk about the airflow speed regulation in purification engineering

Talk about the airflow speed regulation in purification engineering

Purification engineering refers to controlling the cleanliness and temperature and humidity of the atmosphere that products (such as silicon chips, etc.) come into contact with, so that the products can be produced and manufactured in a good environmental space.

Airflow velocity refers to the airflow velocity in the purification project clean room modular. Since it mainly relies on the dilution of air to reduce the degree of indoor pollution, the concept of the number of air changes is mainly used instead of the concept of velocity directly. There are also the following requirements;

(1) The airflow speed at the outlet of the air outlet should not be too large. Compared with a simple air-conditioned clean room modular, the faster the speed decay is required, the larger the diffusion angle is.

(2) The velocity of the airflow over the horizontal plane (for example, the recirculation velocity during side feeding) should not be too large, so as not to blow surface particles back into the airflow and cause re-contamination. Generally, the velocity should not be greater than 0.2m/s.

For the parallel flow purification engineering clean room modular, the speed on the cross-section is a very important indicator because the extrusion of the piston of the airflow is mainly used to eliminate the dyeing.

are important in ensuring extraction machine, and the machine is utilised by everyone from extraction machine to extraction machine.

SUZHOU PHARMA MACHINERY CO.,LTD. will be familiar with the transformation from a generalist into a manufacturer, and will have the big-picture perspective necessary to stay focused on long-term goals.

What SUZHOU PHARMA MACHINERY CO.,LTD. discovered was that innovation occurs when business models match up with one or more of the CUSTOM SOLUTION SERVICES where technological advances overlap with market needs, thus resulting in growth and transformation.

We want to be careful and deliberate about developing PHARMA, from the platform we choose, to the way we approach it, to the methods we use.

There are ample scientific evidence of reducing the risk of extraction machine.

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