/npsi/ctrl?lang=en http://nparc.cisti-icist.nrc-cnrc.gc.ca/npsi/ctrl?lang=fr Access and use of this website and the material on it are subject to the Terms and Conditions set forth at http://nparc.cisti-icist.nrc-cnrc.gc.ca/npsi/jsp/nparc_cp.jsp?lang=en NRC Publications Archive Archives des publications du CNRCThis publication could be one of several versions: author's original, accepted manuscript or the publisher's version. / La version de cette publication peut être l'une des suivantes : la version prépublication de l'auteur, la version acceptée du manuscrit ou la version de l'éditeur. For the publisher's version, please access the DOI link below./ Pour consulter la version de l'éditeur, utilisez le lien DOI ci-dessous.http://dx.doi.org/10.1021/am403222u ACS Applied Materials & Interfaces, 5, 17, pp. 8796-8804, 2013-08-09 Adsorption and desorption of Methylene blue on porous Carbon monoliths and nanocrystalline cellulose He, Xiaoyun; Male, Keith B.; Nesterenko, Pavel N.; Brabazon, Dermot; Paull, Brett; Luong, John H. T. ABSTRACT:The dynamic batch adsorption of methylene blue (MB), a widely used and toxic dye, onto nanocrystalline cellulose (NCC) and crushed powder of carbon monolith (CM) was investigated using the pseudo-first-and -second-order kinetics. CM outperformed NCC with a maximum capacity of 127 mg/g compared to 101 mg/g for NCC. The Langmuir isotherm model was applicable for describing the binding data for MB on CM and NCC, indicating the homogeneous surface of these two materials. The Gibbs free energy of −15.22 kJ/mol estimated for CM unravelled the spontaneous nature of this adsorbent for MB, appreciably faster than the use of NCC (−4.47 kJ/mol). Both pH and temperature exhibited only a modest effect on the adsorption of MB onto CM. The desorption of MB from CM using acetonitrile was very effective with more than 94 % of MB desorbed from CM within 10 min to allow the reusability of this porous carbon material. In contrast, acetonitrile was less effective than ethanol in desorbing MB from NCC. The two solvents were incapable of completely desorbing MB on commercial granular coal-derived activated carbon.

3D printing technology is now frequently employed in many areas of research and development. However, a relatively narrow range of 3D printable materials with a limited spectrum of physico-chemical properties still restricts the true potential of this potentially disruptive technology. There is rapidly increasing interest in the improvement and diversification of properties of generic printing materials via the introduction of fillers with unique properties, and/or by blending materials exhibiting different properties to generate high performance composites. 3D printed composites have already been utilised in a wide range of applications, including biomedical, mechanical, electrical, thermal and optically enhanced products. The increasing popularity of 3D printed composites can be attributed to the ability to fabricate complex geometries, low cost production, and other advantages associated with rapid prototyping. This review covers all the recent reports in which the properties of generic 3D printable materials have been modified either by adding nanoparticles, fibers, other polymers, or by a chemical reaction for fabrication of composites with enhanced biometerial, mechanical, electrical, thermal, optical and other properties.

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