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The formula for calculating the addition of aluminum oxide to the air jet sieve and airflow screening instrument has been under development since 2017. 510-178
Date: 2023-06-06Read: 0

The formula for calculating the addition of aluminum oxide to the air jet sieve airflow screening instrument 510-178 has been under development since 2017. Air jet screening is different from traditional mechanical vibration screening. During the sample dispersion process, if the sample is prone to agglomeration, such as lactose, it is easy for the sample to agglomerate during the screening process. However, it is not possible to use mechanical screening to remove agglomerated dispersed balls from some samples because the power of the air jet screen is limited and cannot blow up these dispersed balls. Therefore, Huimeike added aluminum oxide according to international popular practices and experience to remove static electricity and agglomerates. The formula for the ratio is 1% of the total weight, which is consistent with the error range required by the standard. Under the guidance of the extensive testing experience accumulated by Huimeike over the past 6 years, the testers of the air jet screening method can quickly operate the Huimeike air jet screening airflow screening instrument and achieve the desired screening effect.

Pharmaceutical equipment such as Huimeike air jet screen is a key factor in implementing drug formulation production operations. The sealing type, performance, and automation level of pharmaceutical equipment such as HMK-200 intelligent air jet screen directly affect drug quality and the implementation of GMP system. The production operations and pharmaceutical equipment for different dosage forms are mostly different, and the selection of equipment for the same operating unit is often of multiple types and specifications. Mastering the working principles and structural characteristics of various types of pharmaceutical equipment, such as air jet screening method, according to different dosage forms and their process flow, is an important condition for ensuring the production of high-quality drug particle size detection.

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