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Polyethersulfone

Polyethersulfone Microfiltration Cassettes

The polyethersulfone microfiltration cassettes membrane is a membrane polymer that is well established in the biotechnological and pharmaceutical industries. The polyethersulfone microfiltration cassette is a stable polymer that features a broad pH and temperature range.

Product Introduction

Description
The polyethersulfone microfiltration cassettes membrane is a membrane polymer that is well established in the biotechnological and pharmaceutical industries. The polyethersulfone microfiltration cassette is a stable polymer that features a broad pH and temperature range. Membrane regeneration, storage and depyrogenation can be accomplished by using NaOH even at elevated temperatures. Because of these features, the polyethersulfone microfiltration cassettes are ideally suited for biotechnological applications. polyethersulfone microfiltration cassettes are available in 0.1 µm. Polyethersulfone microfiltration cassettes are designed for applications in the biotechnological and pharmaceutical industries.


They can be used to remove the following cells from liquids:
1)Mammalian cells
2)Clostridia
3)Yeasts
4)Salmonella
5)Mycoplasma reduction

Product Profile
Membrane retention is unaffected by repeated re-use.

Feature

benefits

Low adsorption

Minimal loss of proteins

Low protein-binding

High product yield

Wide pH and a wide variety of temperature range

Chemicals can be used for the removal of foulants

High flow rates

Economical filtration runs

Self sealing cassette

No gaskets needed

Silicone sealing compound

No glue

Enlarged inlet and outlet hole

Lower pressure drop


Specifications
Materials of construction

Membrane

polyethersulfone

Gaskets

pvdf ort Thermoplastic elastomer

Spacer

polipropylene

Preservative

1.6% Phosphoric Acid,
1.1% Acetic Acid,
20% glycerin and water

Sealing compound

Silicone white

Operating Parameters

Maximum Inlet Pressure:

≤4.2bar(60.9 psi)

Forward Transmembrane Pressure

5.5 bar (80 psi) at 4-45 °C,
220 hours continuous(3 hours continuous,0.1m2 format only) 2.5 bar (40 psi) at 4-50 °C, 50 hours continuous

Reverse Transmembrane Pressure:

30 psi (2.1 bar) at 25 °C,
3 min intervals, 10 cycles
(5 cycles, micro format only)

Maximum Caustic Exposure:

1.0 N NaOH at 50 °C
(Contact us for exposure parameters.)

PH Range:

1-14

Nominal Dimensions

Filtratuion area(nominal)

Length(cm)

width(cm)

thickness(cm)

0.1㎡

20.8

5.5

2.2

0.5㎡

20.8

5.5

2.5

1.3㎡

20.8

180

4.0

2.5㎡

20.8

180

7.8

3.5㎡

20.8

180

10.5

Regulatory Information

Component Material Toxicity

Component materials were tested and meet the criteria of the USP <88> Biological Reactivity Tests for Class VI Plastics.

Good Manufacturing Practices

These products are manufactured in a facility which adheres to CFDA Good Manufacturing Practices.

ISO® 9001 Quality Standard:

This product was manufactured in a facility whose Quality Management System is approved by an accredited registering body to the appropriate ISO® 9001 Quality Systems Standard

100% Integrity Tested
in Manufacturing:

Each unit must pass an integrity test based on air flow through the fully-wetted membranes of the filter.

Validated Production Process:

This product was fabricated using a validated manufacturing process. Principles of statistical process control and determinations of process capability have been applied to critical variables in the device fabrication process. In-process controls are used to assure stability of the process.


Sterilization
1.Regulatory Compliance
All materials have passed the USP Biological Test. The filtrate meets or exceeds the currently valid USP and EP for sterile Water for Injection, with respect to particulate matter, extractable substances oxidizable substances, pH dependent maximum conductivity, Ammonia, Chloride, Sulfate, Calcium and Bacteria Endotoxins.
2.Quality Control
Each filter cassette is individually assigned a serial number, integrity tested and certified. It complies with GMP requirements for non-fiber-releasing filters and is filed under the Drug Master File Number DMF 5967 by the Food and Drug Administration, Washington, DC. Validation information is available upon request. If you use holding devices from other suppliers, please contact our Applications Department. A different torque might be needed due to specific variations in design. For further assistance, please contact your local Guidling field engineer or our Goettingen- based Applications Department in China
3.Average Dynamic Water Flux
Permeate* 1550 l/h/m2
* Feed pressure, Pin = 29 psi|2.0 bar; retentate pressure, Pout = 7 psi|0.5 bar

Order Information

Pore size

0.11㎡filter area

0.5㎡filter area

1.3㎡filter area

2.5㎡filter area

0.1um

G01100010M

G05000010M

G13000010M

G25000010M

0.22um

G01100022M

G05000022M

G13000022M

G25000022M

0.45um

G01100045M

G05000045M

G13000045M

G25000045M

0.65um

G01100065M

G05000065M

G1300065M

G25000065M


FAQ
1. Sample service
We have enough samples for our customer in our stock , but need to pay for samples, we can delivery the samples in 7 days.
2. What kind of shipping do you have?
DHL,FEDEX, or by sea .
3. If the products have some quality problem, how will you deal with it?
Each step of production and finished products will be inspected by QC department before shipping. If the quality problem of products caused by us, we will provide a replacement service.

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