Ultrafiltration equipment

Ultra-filtration (Ultra-filtration, UF) is a membrane separation technology that can purify and separate solutions. The ultrafiltration membrane system is a solution separation device with ultrafiltration membrane filaments as the filter medium and the pressure difference on both sides of the membrane as the driving force. Ultrafiltration membranes only allow solvents (such as water molecules), inorganic salts, and small-molecule organic substances in the solution to permeate, while retaining macromolecular substances such as suspended solids, colloids, proteins, and microorganisms in the solution, so as to achieve the purpose of purification or separation.

Advantage

A. The ultrafiltration membrane elements adopt the products of world-renowned membrane companies to ensure that customers get the world's highest quality organic membrane elements, thereby ensuring retention performance and membrane flux.

B. The recovery rate of the system is high, and the quality of the products obtained is excellent, which can realize the efficient separation, purification and high-fold concentration of materials.

C. There is no phase change during the treatment process, no adverse effect on the composition of the material, and the separation, purification, and concentration process is always at room temperature. It is especially suitable for the treatment of heat-sensitive substances, which completely avoids the destruction of biologically active substances by high temperature. Disadvantages, effectively retain the biologically active substances and nutrients in the raw material system.

D. The system has low energy consumption and short production cycle. Compared with traditional process equipment, the equipment operation cost is low, which can effectively reduce the production cost and improve the economic efficiency of the enterprise.

E. The system has advanced technological design, high degree of integration, compact structure, less floor space, simple operation and maintenance, and low labor intensity.

F. The system is made of sanitary pipes and valves, and the site is clean and hygienic, meeting the requirements of GMP or FDA production specifications.

G. The control system can be individually designed according to the user's specific requirements, combined with advanced control software, on-site centralized monitoring of important process operating parameters, to avoid manual misoperation, and multi-directional to ensure the long-term stable operation of the system.