Tapflo are now launching the first membrane pump in the company's new aseptic series.
Features & benefits
- No horizontal areas – no bacteria growth
- Designed for CIP and SIP cleaning - easy cleaning and draining
- Gentle pumping – no damage of sensitive products
- Housings made from electro polished stainless steel AISI 316L, Ra 0.8 (standard) or Ra 0.5 on request - Hygienic surfaces
- Wide range of connection types available: TriClamp, sanitary threads (DIN, SMS) etc - Flexible installation
- No rotating shaft seals - no leakage
- Self priming - flexible installation
- Conform with the ATEX directive - Safe in explosion hazardous areas
- Can run dry and against closed valve without damage - reliable in service
The series will be available in three sizes for sterile applications in primarily the pharmaceuticals, bio-technology and foodstuffs industries.
Owing to its special design this is the first Tapflo series to be approved according to EHEDG regulations.
The EHEDG certificate
The EHEDG (European Hygienic Engineering & Design Group) certificate is your guarantee that the design is according to the hygienic guidelines. Furthermore the pump is clean ability tested, which means bacteria does not grow in the pump after cleaning and draining procedure. Options Can bedelivered witn backup diaphragm system.
|Industry||Example of application|
|Food & dairy|| Soup, cream, syrup, dairy products,
flavoring, alcohol, chocolate, paste
|Pharmaceutics & cosmetics|| Cream, paste, alcohol
and filtration gel
Material of components
|AISI 316L, Ra 0.8
Ra 0.5 on request
|Diaphragms||Diaphragms PTFE (FDA & USP VI)
EPDM (FDA on reguest)
White EPDM (FDA)
PTFE with white back
(FDA & USP VI)
|Valve ball||PTFE (FDA)
PTFE (USP VI & FDA)
EPDM (FDA on request)
EPDM (USP VI & FDA)
|Max flow||94 l/min||144 l/min||330 l/min|
|Max pressure||8 bar||8 bar||8 bar|
|Max air pres-||8 bar||8 bar||8 bar|
|Dry suction lift||2 m||3 m||4.4 m|
|Max solid size||6 mm, bigger||6 mm, big- ger if soft||10 mm, big- ger if soft|
|Temperature||-20˚ .... +110˚C (temporary higher)|
|Weight||15 kg||22 kg||46 kg|
|Connections||Triclamp (standard), SMS, DIN and RJT|
|threads, DIN 11864 clamp|
|ATEX details||Group II, cat 2, T4|
|A||DN 40||DN 50||DN 65|
|Housing,||AISI 316L, Ra 0.8|
|manifolds||Ra 0.5 on request|
|Diaphragms||PTFE (FDA & USP VI)|
|PTFE 1705B (solvents, FDA & USP VI) EPDM (FDA on reguest)|
|White EPDM (FDA)|
|PTFE with white back (FDA & USP VI)|
|Valves (ball type)||PTFE (FDA)|
|PTFE (USP VI & FDA) EPDM (FDA on request) AISI 316L|
|EPDM (USP VI & FDA) FEP/FKM (FDA)|
|Options||Backup diaphragm system|
USP VI approved materials (OPTION)
U.S. Pharmacopeial Convention (USP) class I to VI defines how a plastic or rubber material may be exposed of human tissue. Class VI requires the most stringent testing and such materials may be used for example in implant devices.
EHEDG certified products
The EHEDG (European Hygienic Engineering & Design Group) certificate proves that the design is according to the hygienic guidelines. Furthermore certified products are clean ability tested.
FDA §21 CFR 177 materials
FDA (U.S. Food and Drug Administration) §21 CFR 177 lists polymers, e.g. rubber and plastic materials approved for equipment in contact with food products.
EN 10204 material traceability
The EN 10204 norm gives you a checklist and traceability of materials used in the equipment. 2.1 is a general statement of compliance with material specifications, while 3.1 provides specific track records all the way to the steel mill batch (normally only on metals in contact with the product).
EC 1935/2004 regulation
This EU regulation applies to all food contact materials, e.g. metals, plastics and rubber materials. It requires that these materials are safe, are labeled with the glass-and-fork symbol, are traceable throughout the production chain (according to above EN 10204) and that they are produced according to good manufacturing practice (GMP).
A product classified as machinery that carries the CE mark fulfill the essential health and safety requirements of the EC Machinery Directive 2006/42/EEC.
ATEX Directive 94/9/EC
Equipment intended and approved for safe operation in potentially explosive atmospheres. The equipment is divided in main groups, categories, apparatus groups and temperature classes to define its suitability in the actual zone.