Single-layer Cartridge Filter(MCE 0.2μm)
Product Introduction
Alioth Aligard® MHF Single-layer Cartridge Filter is made from mixed cellulose ester. It has a nominal filtration accuracy of 0.2 μm, a sturdy structure and stable material. It can efficiently retain pollutants, effectively remove particles and colloidal contaminants, block no important active ingredients, protect downstream filtration equipment, and prevent premature clogging.
Product Properties
- Fast flow rate
- High capacity
- No fiber release
- Can withstand multiple cycles of high-temperature sterilization
Typical Applications
- Pre-filtration of culture media and buffer solutions
- Pre-filtration of LVP/SVP
- Pre-filtration of blood products
- Pre-filtration for column protection, etc.
Flow Characteristics
This filter is produced in a controlled environment, and its manufacturing process conforms to ISO9001 quality system standards. Each filter undergoes an integrity testing during the process of manufacturing.
Product Characteristics
| Size (i.e., length) | 10 inch / 20 inch / 30 inch |
| Structural Materials |
Filter membrane：Mixed Cellulose Ester Supporting layer：Polypropylene O-ring：Silicone Cartridge body and end caps：Polypropylene Liner：Polypropylene |
| Pore size | 0.2 μm |
| Filtration area | 10 inch 0.68 m2 / 20 inch 1.32 m2/ 30 inch 2.04 m2 |
| Maximum tolerated differential pressure during operation |
Forward: 5 bar ( 72.5 psi ) @ 25℃ / 1.5 bar ( 21.75 psi ) @ 80℃ / Reverse: 2 bar ( 29 psi ) @ 25℃ |
| Sterilization parameters | 121℃, 30 minutes, 5 cycles of high-pressure sterilizations or 5 cycles of sterilization in place |
| 24-hour dynamic leaching (40-45℃) |
Water: ~20 mg / 10 inch Ethanol: water ( 50：50 ): ~55 mg / 10 inch |
| Biological safety | All the construction components of this cartridge comply with the requirements for biological safety of Class VI plastics in current USP < 88 > |
| Indirect food additive | The primary construction components of this cartridge comply with the reguirements for food contact materials as stipulated in EU 1935 / 2004 / EC and FDA 21 CFR 177-182 |
| Cleanliness | Cleanliness meets the requirements for nonfiber releasing filter as specified in FDA 21 CFR 211.72 and 210.3 (b) (5) (6), and the level of insoluble particles in rinsing liquid meets the requirements of USP < 788 > |
| Endotoxin | The endotoxin level of cartridge rinsing liquid is < 0.25 EU/mL as indicated by gel method, which complies with the requirements of USP < 85 > |
| Integrity | Each filter has passed the integrity test |
| Manufacturing environment | All filters are manufactured in a Class 100,000 clean workshop |
| TOC / Conductivity | TOC < 0.5 mg/L, Conductivity < 1.3 μS/cm |
Ordering Information
For further information, please contact us and Alioth technical team will provide a comprehensive service for your filtration process.
