2013
DOI: 10.1016/j.jfoodeng.2012.09.011
|View full text |Cite
|
Sign up to set email alerts
|

Study on the dissolution of heat-induced ovalbumin gel in alkaline solutions relevant to the removal of fouling deposits

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
3
0

Year Published

2013
2013
2023
2023

Publication Types

Select...
7

Relationship

2
5

Authors

Journals

citations
Cited by 12 publications
(3 citation statements)
references
References 45 publications
0
3
0
Order By: Relevance
“…These results confirmed that 0.5% NaOH is effective in the removal of protein‐based deposits given the range of parameters investigated. Previous studies also reported an optimum NaOH concentration as 0.5% for effective removal of protein‐based deposits (Li et al., 2013; Tuladhar et al., 2002; Xin et al., 2002).…”
Section: Resultsmentioning
confidence: 88%
“…These results confirmed that 0.5% NaOH is effective in the removal of protein‐based deposits given the range of parameters investigated. Previous studies also reported an optimum NaOH concentration as 0.5% for effective removal of protein‐based deposits (Li et al., 2013; Tuladhar et al., 2002; Xin et al., 2002).…”
Section: Resultsmentioning
confidence: 88%
“…The techniques described here could be used to establish how swelling (and shrinkage, Mercadé-Prieto et al, 2007) relate to changes in adhesion strength as well as protein release, and to elucidate why some proteins do not exhibit a concentration optimum (e.g. egg albumin, Li et al, 2013) Alternately, the techniques could be used to probe the change in structure and adhesion in a growing layer, such as a fouling deposit (although the millimanipulation testing, being destructive, would require samples to be provided at different ages), along the lines reported by Bohnet and co-workers (1991) for crystallisation fouling deposits.…”
Section: Discussionmentioning
confidence: 99%
“…Essentially OVA solution (3 wt%) or WPC solution (6 wt%) was used, respectively, in each of the fouling experiments. Detailed procedures are described by Li et al [18,19]. The solution was pumped to the pre-heated section, set at 65 ± 0.5 • C to ensure an inlet temperature of 60 ± 0.5 • C. After the pre-heating, the solution was passed through the heating -monitoring section (the fouling section).…”
Section: Generation Of Protein Foulingmentioning
confidence: 99%