Impact of Protein Removal by an Upstream Ultrafiltration on the Reverse Osmosis of Skim Milk and Sweet Whey

2016 ◽  
Vol 88 (5) ◽  
pp. 585-590 ◽  
Author(s):  
Patricia Meyer ◽  
Ulrich Kulozik
Keyword(s):  
2021 ◽  
Vol 300 ◽  
pp. 110511
Author(s):  
Herehau Blais ◽  
Quang Tri Ho ◽  
Eoin G. Murphy ◽  
Karin Schroën ◽  
John T. Tobin

2020 ◽  
pp. 59-68
Author(s):  
Svetlana Ryabtseva ◽  
Yulia Tabakova ◽  
Andrey Khramtsov ◽  
Georgy Anisimov ◽  
Vitalii Kravtsov

Introduction. Microorganisms of dairy raw materials tend to adhere to the surfaces of processing equipment and form sustainable biofilms, which is a serious issue in the dairy industry. The goal of the present work was to investigate formation of biofilms on a glass surface in static model conditions, and removal of such biofilms by cleaning. Study objects and methods. The study objects were the permeates of skim milk, sweet whey and acid whey, as well as the biofilms formed and washings from glass slides. Biofilms were removed from the glass with detergents used in the dairy industry. Standard methods of determining microbiological and physicochemical properties were used to characterize the permeates. The biofilm structure and morphology of microorganisms participating in biofilm formation were investigated with a light spectroscopy. The efficiency of biofilm removal in a cleaning process was quantified with optical density of washings. Results and discussion. Biofilms in whey permeates formed slower compared to those in skimmed milk permeate during the first 24 h. Yeasts contributed significantly to the biofilm microflora in acid whey permeate throughout 5 days of biofilm growth. Well adhered biofilm layers were the most stable in skimmed milk permeate. The highest growth of both well and poorly adhered biofilm layers was observed in sweet whey permeate after 3–5 days. It was established that the primary attachment of microorganisms to a glass surface occurred within 8 h, mature multicultural biofilms formed within 48 h, and their partial destruction occurred within 72 h. Conclusion. The research results can be used to improve the cleaning equipment procedures in processing secondary dairy raw materials.


2012 ◽  
Vol 43 (1-3) ◽  
pp. 52-62 ◽  
Author(s):  
Habib Bouzid ◽  
Murielle Rabiller-Baudry ◽  
Zoubir Derriche ◽  
Noreddine Bettahar
Keyword(s):  

1973 ◽  
Vol 36 (1) ◽  
pp. 31-33 ◽  
Author(s):  
J. H. Woychik ◽  
M. V. Wondolowski

The β-galactosidase of Aspergillus niger was immobilized by glutaraldehyde coupling to porous glass beads and the bound enzyme evaluated for its applicability to hydrolysis of lactose in milk and milk products. Lactose in sweet whey and skim milk was hydrolyzed at approximately one-third the rate in acid whey. Non-lactose solids inhibited β-galactosidase activity. Greater efficiency of lactose hydrolysis was obtained with the bound enzyme in column operations than in stirred batch reactors.


1983 ◽  
Vol 46 (9) ◽  
pp. 769-770 ◽  
Author(s):  
D. M. BARBANO ◽  
M. W. DUBENSKY ◽  
W. F. SHIPE

Rapid, simple, accurate and cost-effective analytical methods are always needed for quality control in the dairy industry. Application of reverse osmosis for concentration of milk will create a need for a method to rapidly estimate the total solids content of milk retentates. A milk cryoscope can be used for this purpose. An excellent correlation (.99) exists between observed freezing point of skim milk retentates and their total solids content. As a result, it would be possible to have a production worker actually do this total solids monitoring using a milk cryoscope while operating a reverse osmosis unit.


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