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4th EucheMs chemistry congress

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Poster Session 2<br />

s1253<br />

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

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

P - 0 7 8 1<br />

inteGrAted 3d-Printed reACtionwAre for<br />

CheMiCAL SyntheSiS And AnALySiS<br />

M. h. roSneS 1 , P. J. KitSon 1 , M. d. SyMeS 1 ,<br />

v. drAGone 1 , L. Cronin 1<br />

1 University of Glasgow, School of Chemistry, Glasgow, United<br />

Kingdom<br />

Email: Lee.Cronin@glasgow.ac.uk<br />

3D-printing has the potential to transform science and<br />

technology creating bespoke, low-cost appliances which have<br />

previously required dedicated facilities. An attractive but<br />

unexplored application is using the 3D-printer to initiate chemical<br />

reactions by printing the reagents directly into the<br />

3D-reactionware matrix, putting reactionware design,<br />

construction and operation under digital control. In this<br />

contribution, we desecribe how by using a low-cost 3D-printer<br />

and open-source design software, we produced reactionware for<br />

organic and inorganic synthesis, including printed-in catalysts,<br />

and other architectures with printed-in components for<br />

electrochemical and spectroscopic analysis. This allowed<br />

reactions to be monitored in situ so that different reactionware<br />

architectures could be screened for their efficacy for a given<br />

process, giving a digital feed-back mechanism for device<br />

optimisation. Furthermore, by solely modifying reactionware<br />

architecture, reaction outcomes could be drastically altered. Taken<br />

together, this approach constitutes a cheap, automated and<br />

reconfigurable chemical discovery platform that makes techniques<br />

from chemical engineering accessible to typical synthetic<br />

laboratories. [1] It is even conceivable that this approach could be<br />

used to undertake complex reactions and allow the reliable access<br />

to <strong>chemistry</strong> beyond the laboratory created in the ‘reactionware’<br />

environment and the prospects for this will be discussed.<br />

references:<br />

1. M. D. Symes, P. J. Kitson, J. Yan, C. J. Richmond,<br />

G. J. T. Cooper, R. W. Bowman, T. Vilbrandt, L. Cronin,<br />

Nature Chem. 2012, 4, 349-354.<br />

Keywords: Inorganic Chemistry; Multicomponent reactions;<br />

Polymers;<br />

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

P - 0 7 8 2<br />

effeCt of the AL o And BAo Addition on the<br />

2 3<br />

therMAL And PhySiCAL ProPertieS of<br />

ternAry GLASS SySteM<br />

B. SAfi 1 , M. MAALeM 2 , d. ABoutALeB 1 , M. SAidi 1<br />

1 Boumerdes University, Materials Engineering, Boumerdes,<br />

Algeria<br />

2 Boumerdes University, Process Engineering, Boumerdes,<br />

Algeria<br />

In borate glasses, the main structural units are the [BO ] 3<br />

triangles and [BO ] tetradral which form different superstructural<br />

4<br />

units like; boroxol rings, metaborate rings and chains, pentaborate,<br />

diborate, triborate and pyroborate. In this work, the Barium<br />

aluminoborate glasses were prepared. Some of properties were<br />

investigated by measure like density and chemical durability and<br />

the other by calculs. The dilatometric curves were determined and<br />

they revealed that the temperature of transition (Tg) and softening<br />

(Ts) and the dilatation coefficient increase by addition of Al O 2 3<br />

and BaO content.<br />

Keywords: Barium aluminoborate glass; dilatometric curves;<br />

chemical durability; densiy; dilatation coefficient;<br />

AUGUst 26–30, 2012, PrAGUE, cZEcH rEPUbLIc

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