Ultrasonic cleaning of conveyor belt materials using Listeria monocytogenes as a model organism

Riina Tolvanen (Corresponding Author), Janne Lundén, Hannu Korkeala, Gun Wirtanen

Research output: Contribution to journalArticleScientificpeer-review

20 Citations (Scopus)


Persistent Listeria monocytogenes contamination of food industry equipment is a difficult problem to solve. Ultrasonic cleaning offers new possibilities for cleaning conveyors and other equipment that are not easy to clean. Ultrasonic cleaning was tested on three conveyor belt materials: polypropylene, acetal, and stainless steel (cold-rolled, AISI 304). Cleaning efficiency was tested at two temperatures (30 and 45°C) and two cleaning times (30 and 60 s) with two cleaning detergents (KOH, and NaOH combined with KOH). Conveyor belt materials were soiled with milk-based soil and L. monocytogenes strains V1, V3, and B9, and then incubated for 72 h to attach bacteria to surfaces. Ultrasonic cleaning treatments reduced L. monocytogenes counts on stainless steel 4.61 to 5.90 log units; on acetal, 3.37 to 5.55 log units; and on polypropylene, 2.31 to 4.40 log units. The logarithmic reduction differences were statistically analyzed by analysis of variance using Statistical Package for the Social Sciences software. The logarithmic reduction was significantly greater in stainless steel than in plastic materials (P < 0.001 for polypropylene, P = 0.023 for acetal). Higher temperatures enhanced the cleaning efficiency in tested materials. No significant difference occurred between cleaning times. The logarithmic reduction was significantly higher (P = 0.013) in cleaning treatments with potassium hydroxide detergent. In this study, ultrasonic cleaning was efficient for cleaning conveyor belt materials.
Original languageEnglish
Pages (from-to)758-761
JournalJournal of Food Protection
Issue number3
Publication statusPublished - 2007
MoE publication typeA1 Journal article-refereed


Dive into the research topics of 'Ultrasonic cleaning of conveyor belt materials using Listeria monocytogenes as a model organism'. Together they form a unique fingerprint.

Cite this