Team:Oxford/biopolymer containment
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<div style="background-color:#D9D9D9; opacity:0.7; z-index:5; Height:75px; width:100%;font-size:65px;font-family:Helvetica;padding-top:5px; font-weight: 450;margin-top:10px;"> | <div style="background-color:#D9D9D9; opacity:0.7; z-index:5; Height:75px; width:100%;font-size:65px;font-family:Helvetica;padding-top:5px; font-weight: 450;margin-top:10px;"> | ||
- | <div style="background-color:white; opacity:0.9; Height:75px; width:100%;margin-top:5px:margin-bottom:5px;font-size:65px;font-family:Helvetica;padding-top:5px; color:#00000; font-weight: 450;"><br><center><font style="opacity:0.7"> | + | <div style="background-color:white; opacity:0.9; Height:75px; width:100%;margin-top:5px:margin-bottom:5px;font-size:65px;font-family:Helvetica;padding-top:5px; color:#00000; font-weight: 450;"><br><center><font style="opacity:0.7">Biopolymer Containment</font></center></div> |
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<h1>Introduction</h1> | <h1>Introduction</h1> | ||
- | + | The ‘Realisation’ sections of our project aim to bridge the gap between laboratory research and industrial application by the development of a novel biotechnology. Our project aims to synthesise bacteria-containing biopolymer capsules to maximise reaction rate, acting simultaneously as a substrate diffusion barrier, such that the rate of DCM intake is less than or equal to the rate of DCM breakdown by the strain, allowing the capsules to be in direct contact with higher [DCM] while restricting the local bacterial [DCM] to a viable concentration. | |
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- | <h1white> | + | <h1white>Why is this necessary?</h1white></div></a> |
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Revision as of 17:39, 28 September 2014