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4th EucheMs chemistry congress

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Poster Session 2<br />

s1251<br />

chem. Listy 106, s257–s1425 (2012)<br />

Poster session 2 - Nano<strong>chemistry</strong>, Nanotechnology<br />

P - 0 7 7 7<br />

MetAL oxide nAno-SheetS with (111) SurfACeS<br />

AS CAtALyStS And CAtALySt SuPPortS<br />

r. riChArdS 1<br />

1 Colorado School of Mines, Chemistry and Geo<strong>chemistry</strong>,<br />

Golden, USA<br />

The interface of the fields of catalysis and nanoscale<br />

materials is one of the most exciting areas of modern science and<br />

is at the forefront of the quest for a “green” and sustainable future.<br />

Recent progress on new methods to control the size, shape and<br />

composition of nanoscale materials and their application in<br />

renewable energy technologies are particularly intriguing.<br />

Recently, the Richards’ research group has developed techniques<br />

to produce a number of new nanoscale materials that have<br />

demonstrated unique physical and chemical properties through<br />

controlled facetting. Here, recent highlights regarding these<br />

materials and their applications will be presented with a particular<br />

focus towards nanostructured metal oxides. MgO and NiO have<br />

a typical rocksalt structure and although the stoichiometry and<br />

crystallinity change little, the morphology can vary in shape,<br />

particle size and surface structure. The (100) facet of the rocksalt<br />

structure is unambiguously the most stable due to its low surface<br />

energy, therefore, it is unaminously the surface demonstrated by<br />

current wet chemical preparations. Numerous studies have<br />

demonstrated that the shape and size of crystalline MgO and NiO<br />

are highly influential on the adsorption properties. Furthermore,<br />

nanoscale MgO has been reported to be extremely effective for<br />

the destructive adsorption of numerous environmental toxins and<br />

several chemical warfare agents (VX, sarin, mustard gas).<br />

However, the (111) surface consists of alternating polar<br />

monolayers and thus, a strong electrostatic field perpendicular to<br />

the (111) surface is created. Such a surface has provided a<br />

prototype for the study of surface structure and surface reactions,<br />

which drew great attention for both experimental and theoretical<br />

studies. These studies imply the importance of size and shape<br />

control in metal oxide synthesis for their applications.<br />

Keywords: green <strong>chemistry</strong>; nanostructures; Heterogeneous<br />

catalysis; Supported catalysts;<br />

4 th <strong>EucheMs</strong> <strong>chemistry</strong> <strong>congress</strong><br />

P - 0 7 7 8<br />

An effiCient And oPtiMized<br />

AMinoSiLAnizAtion of ti6AL4v ALLoy for<br />

BioMediCAL deviCeS<br />

A. rodríGuez-CAno 1 , M. C. fernández-CALderón 2 ,<br />

M. A. PAChA-oLivenzA 3 , r. BABiAno 4 , P. CintAS 4 ,<br />

M. L. GonzáLez-MArtín 3<br />

1 Universidad de Extremadura. Centro de Investigación<br />

Biomédica en Red en Bioingeniería Biomateriales y<br />

Biomedicina (CIBER-BBN), Química Orgánica e Inorgánica,<br />

Badajoz, Spain<br />

2 Universidad de Extremadura. Centro de Investigación<br />

Biomédica en Red en Bioingeniería Biomateriales y<br />

Biomedicina (CIBER-BBN), Ciencias Biomédicas, Badajoz,<br />

Spain<br />

3 Universidad de Extremadura. Centro de Investigación<br />

Biomédica en Red en Bioingeniería Biomateriales y<br />

Biomedicina (CIBER-BBN), Física Aplicada, Badajoz, Spain<br />

4 Universidad de Extremadura, Química Orgánica e Inorgánica,<br />

Badajoz, Spain<br />

Titanium and titanium alloys are widely employed in biomedical<br />

implants due to their chemical inertia and biocompatibility. [1] The latter<br />

is generally improved by forming thin films of bioactive small molecules<br />

on the metal surface, thus preventing bacterial adhesion which<br />

represents a major concern. A common chemical functionalization of<br />

such alloys involves silanization with organosilanes such as<br />

(3-aminopropyl)triethoxysilane (APTES), thereby resulting in an<br />

aminated surface. Unfortunately, the amount of amino groups<br />

deposited and therefore available to further modification is not<br />

routinely evaluated. Moreover, there is confusion as to which reaction<br />

conditions will produce a stable and densely aminated film. [2]<br />

In this communication we report an efficient and<br />

reproducible methodology for coating Ti6Al4V alloy with<br />

(3-aminopropyl)trimethoxysilane (APTMS). The influence of<br />

reaction time, water concentration, reaction temperature, and<br />

cross-linking conditions on surface coverage was studied.<br />

Ninhydrin assays were systematically employed to assess the<br />

density of amino groups. XPS, FTIR-ATR, and SEM analyses<br />

helped us to determine changes in both surface composition and<br />

roughness.<br />

In addition, bacterial adhesion and biofilm formation of<br />

Staphylococcus ATCC35983 and S. epidermidis ATCC35984<br />

were also evaluated on both silanized disks according to the<br />

above-mentioned protocol and those exposed subsequently to<br />

degradation with PBS. Adhesion and biofilm formation decreased<br />

with respect to oxidized control disks.<br />

Acknowledgments. This work was supported by grants from the<br />

Ministry of Science and Innovation (MAT2009-14695-C04-01,<br />

MAT2009-14695-C04-03 and CTQ2010-18938), Gobierno de<br />

Extremadura (Ayudas a Grupos Consolidados: GR10049 and<br />

GR10149) and FEDER (Fondo Europeo de Desarrollo<br />

Regional, Una Manera de Hacer Europa). One of us (ARC)<br />

thanks the Ministry for a scholarship (BES-2010-033417).<br />

references:<br />

1. Geetha M, Singh AK, Asokamani R, Gogia AK.<br />

Prog Mater Sci 2009, 54, 397-425.<br />

2. Kingshott P, Andersson G, McArthur SL, Grieser HJ.<br />

Curr Op Chem Biol 2011, 15, 667-676.<br />

Keywords: titanium; alloys; material science; self-assembly;<br />

biological activity;<br />

AUGUst 26–30, 2012, PrAGUE, cZEcH rEPUbLIc

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