PubMed · 11285815
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M Fischetti. 2001. Working knowledge. Touch screens.. https://pubmed.ncbi.nlm.nih.gov/11285815/
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Acoustic cell retention devices have provided a practical alternative for up to 50 L/day perfusion cultures but further scale-up has been limited. A novel temperature-controlled and larger-scale acoustic separator was evaluated at up to 400 L/day for a 10(7) CHO cell/mL perfusion culture using a 100-L bioreactor that produced up to 34 g/day recombinant protein. The increased active volume of this scaled-up separator was divided into four parallel compartments for improved fluid dynamics. Operational settings of the acoustic separator were optimized and the limits of robust operations explored. The performance was not influenced over wide ranges of duty cycle stop and run times. The maximum performance of 96% separation efficiency at 200 L/day was obtained by setting the separator temperature to 35.1 degrees C, the recirculation rate to three times the harvest rate, and the power to 90 W. While there was no detectable effect on culture viability, viable cells were selectively retained, especially at 50 L/day, where there was a 5-fold higher nonviable washout efficiency. Overall, the new temperature-controlled and scaled-up separator design performed reliably in a way similar to smaller-scale acoustic separators. These results provide strong support for the feasibility of much greater scale-up of acoustic separations.
Biofilms occur in natural and engineered water systems. Biofouling in technical processes lowers the water quality and increases the frictional resistance in tubes. In wastewater treatment plants, biofilms are used for removal of organic an inorganic pollutants. For improvement of antifouling strategies and for process optimization in wastewater treatments plants, an analytical technique for online monitoring of biofilms is needed. In this article, a new setup for in situ monitoring of biofilms by photoacoustic spectroscopy is presented. To produce a biofilm, a mixture of microorganisms was grown in a nutrient solution inside a tube reactor. The content of the tube reactor was pumped through a flow channel, and biofilms were generated at the inner surfaces. Three photoacoustic sensor heads were integrated at different positions into the base plate of the flow channel. By photoacoustic spectroscopy, growth, thickness, and detachment of biofilms can be monitored on-line and nondestructively. Experiments presented in this article showed that the flow conditions influence the structure and thickness of biofilms. By changing the pH value, electrostatic interactions inside the biofilm matrix were influenced, and the subsequent detachment processes were observed online. The interaction of iron(III) oxide particles with biofilms led to particle adsorption on the outer and inner surfaces of the biofilm. Afterwards, biofilm flocs were sloughed off from the base biofilm.
Breaking ocean waves entrain air bubbles that enhance air-sea gas flux, produce aerosols, generate ambient noise and scavenge biological surfactants. The size distribution of the entrained bubbles is the most important factor in controlling these processes, but little is known about bubble properties and formation mechanisms inside whitecaps. We have measured bubble size distributions inside breaking waves in the laboratory and in the open ocean, and provide a quantitative description of bubble formation mechanisms in the laboratory. We find two distinct mechanisms controlling the size distribution, depending on bubble size. For bubbles larger than about 1 mm, turbulent fragmentation determines bubble size distribution, resulting in a bubble density proportional to the bubble radius to the power of -10/3. Smaller bubbles are created by jet and drop impact on the wave face, with a -3/2 power-law scaling. The length scale separating these processes is the scale where turbulent fragmentation ceases, also known as the Hinze scale. Our results will have important implications for the study of air-sea gas transfer.