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  Controlling heterogeneous ice nucleation with chemical impurities and electrical charge


   Faculty of Environment

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  Prof Benjamin Murray, Prof K Carslaw  No more applications being accepted  Competition Funded PhD Project (Students Worldwide)

About the Project

A fundamental understanding of the nucleation of ice crystals is of importance in a wide range of fields: cryopreservation of biological samples relies in the control of ice nucleation, avoiding ice formation on aircraft and wind turbines is key to their efficient and safe operation, and ice nucleation in clouds is very important for the planet’s climate. However, we have very limited knowledge of why certain materials trigger the formation of ice, while others do not. 

It is thought that specific sites on surfaces which are perhaps just 10’s of nanometers in size are responsible for nucleation, but these sites can occupy only 10-10 % of the surface. Hence, they are incredibly difficult to identify and characterise and our understanding of them remains extremely poor. What makes effective active sites is a key topic

There is evidence that impurities such as lead and iodine may promote nucleation and there are also mechanisms where charge and electric fields can promote ice nucleation. Our hypothesis is that nucleation occurring at specific active sites is related to impurities and/or charge at these sites.

Objectives

i)            Experimentally investigate the role of electrical charge in nucleating ice – this may offer novel means to control ice nucleation and may offer explanations for unexplained high temperature nucleation in clouds;

ii)           investigate the role of minor chemical contaminants in promoting ice nucleation in various materials – there is evidence that suggests the inclusion of elements like lead, strontium and iodine promote nucleation in otherwise inert materials.

iii) apply the knowledge to firstly design materials which might be used in cryopreservation applications and secondly to identify natural materials and situations where enhanced nucleation may occur in the atmosphere.

Biological Sciences (4) Chemistry (6) Engineering (12) Environmental Sciences (13) Physics (29)

Funding Notes

EPSRC DTP 3.5 years fully-funded awards for UK nationals who meet the residency requirements; settled and pre-settled status EU nationals; and those with ILTR in the UK. There is up to one award for overseas applicants, although you should contact the project supervisor before applying if you are in this funding category.

References

Atkinson, J. D., Murray B.J., and Coauthors, 2013: The importance of feldspar for ice nucleation by mineral dust in mixed-phase clouds. Nature, 498, 355-358.
Daily, M. I., Whale, T. F., Partanen, R., Harrison, A. D., Kilbride, P., Lamb, S., Morris, G. J., Picton, H. M., and Murray, B. J.: Cryopreservation of primary cultures of mammalian somatic cells in 96-well plates benefits from control of ice nucleation, Cryobiology, 93, 62-69, 2020.
Holden, M. A., Whale, T. F., Tarn, M. D., O’Sullivan, D., Walshaw, R. D., Murray, B. J., Meldrum, F. C., and Christenson, H. K.: High-speed imaging of ice nucleation in water proves the existence of active sites, Science Advances, 5, eaav4316, 2019.
Morris, G. J. and Acton, E.: Controlled ice nucleation in cryopreservation - A review, Cryobiology, 66, 85-92, 2013.
Murray, B. J., D. O'Sullivan, J. D. Atkinson, and M. E. Webb, 2012: Ice nucleation by particles immersed in supercooled cloud droplets. Chem. Soc. Rev., 41, 6519-6554.
Murray, B. J., Carslaw, K. S., and Field, P. R.: Opinion: Cloud-phase climate feedback and the importance of ice-nucleating particles, Atmos. Chem. Phys. Discuss., 2020, 1-23, 2020.
Wilson, T. W., and Coauthors, 2015: A marine biogenic source of atmospheric ice-nucleating particles. Nature, 525, 234-238.
Whale, T. F., Holden, M. A., Kulak, A. N., Kim, Y.-Y., Meldrum, F. C., Christenson, H. K., and Murray, B. J.: The role of phase separation and related topography in the exceptional ice-nucleating ability of alkali feldspars, Phys. Chem. Chem. Phys., doie: 10.1039/C7CP04898J, 2017. 2017.

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