A Neutron and X‐Ray Diffraction Study of Bioglass® with Reverse Monte Carlo Modelling
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Julian R. Jones | R. Moss | D. Pickup | R. J. Newport | D. Greenspan | J. Fitzgerald | G. Sarkar | K. Wetherall | V. Fitzgerald
[1] G. Mountjoy,et al. Modeling the Local Atomic Structure of Bioactive Sol−Gel-Derived Calcium Silicates , 2006 .
[2] C. Bianchi,et al. Surface modifications of bioglass immersed in TRIS-buffered solution. A multitechnical spectroscopic study. , 2005, The journal of physical chemistry. B.
[3] L. Hench,et al. The use of advanced diffraction methods in the study of the structure of a bioactive calcia: silica sol-gel glass. , 2005, Journal of materials science. Materials in medicine.
[4] A. Boccaccini,et al. Structural analysis of bioactive glasses , 2005 .
[5] Jincheng Du,et al. The medium range structure of sodium silicate glasses: a molecular dynamics simulation , 2004 .
[6] M. Cerruti,et al. Surface chemical functionalities in bioactive glasses. The gas/solid adsorption of acetonitrile , 2004 .
[7] M. Yashima,et al. Crystal structure analysis of β-tricalcium phosphate Ca3(PO4)2 by neutron powder diffraction , 2003 .
[8] M. Cerruti,et al. Characterization of sol–gel bioglasses with the use of simple model systems: a surface-chemistry approach , 2003 .
[9] A. Putnis,et al. Phase transition behaviour and equilibrium phase relations in the fast-ion conductor system Na3PO4 Na2SO4 , 2002 .
[10] J. Cole,et al. An x-ray diffraction and 31P MAS NMR study of rare-earth phosphate glasses, (R2O3)x(P2O5)1-x, x = 0.175-0.263, R = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er , 2001 .
[11] L L Hench,et al. Gene-expression profiling of human osteoblasts following treatment with the ionic products of Bioglass 45S5 dissolution. , 2001, Journal of biomedical materials research.
[12] J. Polak,et al. Ionic products of bioactive glass dissolution increase proliferation of human osteoblasts and induce insulin-like growth factor II mRNA expression and protein synthesis. , 2000, Biochemical and biophysical research communications.
[13] A. Hannon,et al. The P-O bond lengths in vitreous probed by neutron diffraction with high real-space resolution , 1998 .
[14] D. Holland,et al. NMR investigation of the structure of some bioactive and related glasses , 1995 .
[15] A. Kentgens,et al. 23Na NMR Spectroscopy of Solids: Interpretation of Quadrupole Interaction Parameters and Chemical Shifts , 1994 .
[16] J. Stebbins,et al. 23Na NMR chemical shifts and local Na coordination environments in silicate crystals, melts and glasses , 1993 .
[17] C. Simmons,et al. Experimental Techniques of Glass Science , 1993 .
[18] Ilkka Kangasniemi,et al. Calcium phosphate formation at the surface of bioactive glass in vitro. , 1991, Journal of biomedical materials research.
[19] R. L. McGreevy,et al. Reverse Monte Carlo Simulation: A New Technique for the Determination of Disordered Structures , 1988 .
[20] A. Clark,et al. The influence of surface chemistry on implant interface histology: a theoretical basis for implant materials selection. , 1976, Journal of biomedical materials research.
[21] Larry L. Hench,et al. Bonding mechanisms at the interface of ceramic prosthetic materials , 1971 .
[22] N. H. Leeuw,et al. The structure of bioactive silicate glasses : New insight from molecular dynamics simulations , 2007 .
[23] I. L. Mudrakovskii,et al. 31P nmr study of I–IV group polycrystalline phosphates , 1986 .
[24] B. Warren,et al. X-Ray Diffraction , 2014 .