Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Protein fractionation using ultrafiltration is feasible after extensive process optimization. However, conventional process optimisation methods are time consuming and require large amounts of pure proteins, which are sometimes very expensive. Pulsed sample injection ultrafiltration allows rapid determination of sieving coefficient data and may prove to be an efficient process optimisation technique. Very small amounts of pure protein are required for these experiments. A 'quasi-steady state' approximation is proposed for calculating the actual bulk and membrane surface concentrations from permeate concentration data. The sieving coefficient data obtained from the pulsed sample injection technique are in good agreement with data obtained from 'steady-state' ultrafiltration experiments. Experimental data clearly suggest that for a given permeate flux, the sieving coefficients are independent of the value of the feed concentration. The permeate concentration-time curves show that at higher permeate flux, lower time duration is required for the development of concentration polarization. (C) 2000 Elsevier Science B.V.

Original publication

DOI

10.1016/S0376-7388(00)00397-5

Type

Journal article

Journal

Journal of Membrane Science

Publication Date

01/08/2000

Volume

175

Pages

75 - 84