Glantreo synthesise silica. We identified a gap in the market, monodispersed silica without classification.
1. Highly monodispersed without the need to size classify leading to high chromatographic efficiency
2. Monodensity leading to higher packing stability as there are no macro pores within the particles.
3. ‘Hard Silica’ (produced with heat during manufacturing) leads to greater stability and longevity of material and columns.
The foundation of any good chromatography column is the stationary phase. We are experts in stationary phases.
Eiroshell™ is a patent protected product range of highly monodisperse, durable and reproducible porous core-shell silica particles manufactured by Glantreo. Our proprietary process is completely tuneable allowing control over physical properties of the particles including the core and shell dimensions. The technology uses a sol gel templating approach to grow a porous silica layer on the solid silica core.
Whilst the Eiroshell particles have a standard pore size of 100A, we have also augmented the Eiroshell process with our core enlargement technologies to produce a range of pore sizes from 100A to 1000A. These particles have been commercialised in our Eiroshell™ RP and Eiroshell™ Bio Columns.
If you have a custom particle requirement then ‘Ask and Expert’ and we can discuss in more detail.
Purity | 0.9999 |
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Chemistry | C1, C4, C8, C18, C18 plus, C18 Aqua, Bi-Phenyl, Phenyl-hexyl, Phenyl-hexyl plus, PFP, Cyano, Amino, Diol, Silica |
Parcticle Sizes | 1.7um, 2.2um, 2.6um |
d90/d10 | <1.4 |
Pore Size | 100A, 160A, 300A, 1000A |
Pore Volume | 0.25cm3g-1 - 0.35cm3g-1 |
Surface Area | 100m2g-1 to 130m2g-1 |
Carbon Coverage | C18 - 8% C8 - 5% C4 - 3% |
If you have published and cited Glantreo’s materials then click here to let us know.
Benjamin A. Ashu-Arraha, Jeremy D. Glennona,∗, Klaus Albertb, Synthesis and characterisation of bonded mercaptopropyl silica intermediate stationary phases prepared using multifunctional alkoxysilanes in supercritical carbon dioxide as a reaction solvent, Journal of Chromatography A, 1222 (2012) 38–45n
Maressa D. Dolzana,b, Daniel A. Spudeita,b, Zachary S. Breitbacha, William E. Barberc, Gustavo A. Mickeb, Daniel W. Armstronga,d, Comparison of superficially porous and fully porous silica supports used for a cyclofructan 6 hydrophilic interaction liquid chromatographic stationary phase, Journal of Chromatography A, 1365 (2014) 124-30
Szabolcs Feketea,∗, Erzsébet Oláhb, Jeno ̋Feketea, Fast liquid chromatography: The domination of core–shell and very fine particles, Journal of Chromatography A, 1228 (2012) 57–71
Víctor González-Ruiz, Ana I. Olives, M. Antonia Martín, Core-shell particles lead the way to renewing high-performance liquid chromatography, Trends in Analytical Chemistry (2014),
Victor K. Langsi, Benjamin A. Ashu-Arrah, Jeremy D. Glennon, Sub-2-m seeded growth mesoporous thin shell particles for high-performance liquid chromatography: Synthesis, functionalisation and characterisation, Journal of Chromatography A, 1402 (2015) 17–26
Lucie Nováková *, Lucie Havlíková, Hana Vlcˇková, Hydrophilic interaction chromatography of polar and ionizable compounds by UHPLC, Trends in Analytical Chemistry 63 (2014) 55–64
Jesse O. Omamogho, John P. Hanrahan, Joe Tobin, Jeremy D. Glennon, Structural variation of solid core and thickness of porous shell of 1.7µm core–shell silica particles on chromatographic performance: Narrow bore columns, Journal of Chromatography A, Volume 1218, Issue 15, 15 April 2011, Pages 1942-1953, ISSN 0021-9673 http://www.sciencedirect.com/science/article/pii/S0021967310016559
Jesse O. Omamoghoa, John P. Hanrahanb, Joe Tobinb, Jeremy D. Glennon, Structural variation of solid core and thickness of porous shell of 1.7 m core–shell silica particles on chromatographic performance: Narrow bore columns, Journal of Chromatography A, 1218 (2011) 1942–1953
Daniel A. Spudeita,b, Maressa D. Dolzana,b, Zachary S. Breitbacha, William E. Barberc, Gustavo A. Mickeb, Daniel W. Armstrong , Superficially porous particles vs. fully porous particles for bonded high performance liquid chromatographic chiral stationary phases: Isopropyl cyclofructan 6, Journal of Chromatography A, 1363 (2014) 89–95