Fouling at interfaces deteriorates the efficiency and
hygiene of
processes within numerous industrial sectors, including the oil and
gas, biomedical device, and food industries. In the food industry,
the fouling of a complex food matrix to a heated stainless steel surface
reduces production efficiency by increasing heating resistance, pumping
requirements, and the frequency of cleaning operations. In this work,
quartz crystal microbalance with dissipation (QCM-D) was used to study
the interface formed by the fouling of milk on a stainless steel surface
at different flow rates and protein concentrations at high temperatures
(135 °C). Subsequently, the QCM-D response was recorded during
the cleaning of the foulant. Two phases of fouling were identified.
During phase-1, the fouling rate was dependent on the flow rate, while
the fouling rate during phase-2 was dependent on the flow rate and
protein concentration. During cleaning, foulants deposited at the
higher flow rate swelled more than those deposited at the lower flow
rate. The composition of the fouling deposits consisted of both protein
and mineral species. Two crystalline phases of calcium phosphate,
β-tricalcium phosphate and hydroxyapatite, were identified at
both flow rates. Stratification in topography was observed across
the surface of the QCM-D sensor with a brittle and cracked structure
for deposits formed at 0.2 mL/min and a smooth and close-packed structure
for deposits formed at 0.1 mL/min. These stratifications in the composition
and topography were correlated to differences in the reaction time
and flow dynamics at different flow rates. This high-temperature application
of QCM-D to complex food systems illuminates the initial interaction
between proteins and minerals and a stainless steel surface, which
might otherwise be undetectable in low-temperature applications of
QCM-D or at larger bench and industrial scales. The methods and results
presented here have implications for optimizing processing scenarios
that limit fouling formation while also enhancing removal during cleaning.
Molecular details
concerning the induction phase of milk fouling
on stainless steel at an elevated temperature range were established
to better understand the effect of temperature on surface fouling
during pasteurization. The liquid–solid interface that replicates
an industrial heat exchanger (≤75°C), including four stages
(preheating, heating, holding, and cooling), was investigated using
both a quartz crystal microbalance (QCM-D) and a customized flow cell.
We found that the milk fouling induction process is rate-limited by
the synergistic effects of bulk reactions, mass transfer, and surface
reactions, all of which are controlled by both liquid and surface
temperatures. Surface milk foulant becomes more rigid and compact
as it builds up. The presence of protein aggregates in the bulk fluid
leads to a fast formation of surface deposit with a reduced Young’s
modulus. Foulant adhesion and cohesion strength was enhanced as both
interfacial temperature and processing time increased, while removal
force increased with an increasing deposit thickness. During cleaning,
caustic swelling and removal showed semilinear correlations with surface
temperature (
T
S
), where higher
T
S
reduced swelling and enhanced removal. Our
findings evidence that adsorption kinetics, characteristics of the
foulant, and the subsequent removal mechanism are greatly dependent
on the temperature profile, of which the surface temperature is the
most critical one.
The thermal processing of milk is negatively impacted by fouling, which decreases the rate of heat transfer and increases the frequency of cleaning. Small-scale tools that can predict fouling on larger scales are crucial to understanding and mitigating fouling. In this work, milk fouling is compared between the submicron scale, using a high-pressure high-temperature quartz crystal microbalance with dissipation (HPHT QCM-D), and the pilot scale. Fouling rates are monitored in situ and foulants are characterized ex situ using Raman spectroscopy and atomic force microscopy (AFM). The results reveal that a proteinaceous foulant is formed on both scales. Also, a gradient in the magnitude of fouling is observed at both scales as a function of the local residence time and temperature with the greatest amount of fouling observed for the smallest local residence time and at the highest temperature (132 °C). The results suggest a scale-up factor of approximately 70−120 times when converting between QCM-D and pilot-scale fouling thicknesses. Similarities in the foulant properties and fouling rates support QCM-D as a viable technology for scale-up studies of milk fouling.
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