Articles
Permanent URI for this collectionhttps://laurentian.scholaris.ca/handle/10219/2545
Browse
Recent Submissions
Item High-performance iron oxide-graphene oxide nanocomposite adsorbents for arsenic removal(2017-01-01) Ye, Zhibin; Su, Hui; Hmidi, NuriWe report the synthesis of a new range of iron oxide-graphene oxide (GO) nanocomposites having different iron oxide content (36–80 wt%) as high-performance adsorbents for arsenic removal. Synthesized by co-precipitation of iron oxide on GO sheets that are prepared by an improved Hummers method, the iron oxide in the nanocomposites is featured primarily in the desirable form of amorphous nanoparticles with an average size of ca. 5 nm. This unique amorphous nanoparticle morphology of the iron oxide beneficially endows the nanocomposites with high surface area (up to 341 m2 g-1 for FeOx-GO-80 having the iron oxide content of 80 wt%) and predominant mesopore structures, and consequently increased adsorption sites and enhanced arsenic adsorption capacity. FeOx-GO-80 shows high maximum arsenic adsorption capacity (qmax) of 147 and 113 mg g−1 for As(III) and As(V), respectively. These values are the highest among all the iron oxide-GO/reduced GO composite adsorbents reported to date and are also comparable to the best values achieved with various sophisticatedly synthesized iron oxide nanostructures. More strikingly, FeOx-GO-80 is also demonstrated to nearly completely (>99.98%) removes arsenic by reducing the concentration from 118 (for As(III)) or 108 (for As(V)) to < 0.02 μg L−1, which is far below the limit of 10 μg L−1 recommended by the World Health Organization (WHO) for drinking water. The excellent adsorption performance, along with their low cost and convenient synthesis, makes this range of adsorbents highly promising for commercial applications in drinking water purification and wastewater treatment.Item Ultra-small carbon nanospheres (< 50 nm) of uniform tunable sizes by a convenient catalytic emulsion polymerization strategy: superior supercapacitive and sorption performances(2013-01-01) Ye, Zhibin; Tiwari, Vimal K.; Chen, Zhe; Gao, Fan; Gu, Zhiyong; Sun, XueliangPorous carbon nanospheres have received enormous attention for various applications. Though there are several elegant strategies existing for the synthesis of relatively large carbon nanospheres (> ca. 100 nm), the synthesis of carbon nanospheres with well-defined tunable ultra-small sizes (< 50 nm) has often been challenging while such ultra-small nanospheres are much more valuable. A novel, convenient, and scalable catalytic emulsion polymerization technique is demonstrated in this paper for highly efficient synthesis of ultra-small carbon nanospheres with uniform tunable sizes in the range of 11–38 nm. In this strategy, a simple change of the emulsion polymerization recipe renders a convenient yet efficient tuning of the size of the carbon nanospheres. In particular, activated carbon nanospheres (A-CNS21 of average size of 21 nm) obtained by carbonization in the presence of KOH as the chemical activation agent is featured with very high surface area (2,360 m2/g) and the desired hierarchical macro-/meso-/micropore structures resulting from nanosphere packing/aggregation. A-CNS21 is demonstrated to have superior high-rate supercapacitive performances and outstanding sorption capacities towards volatile organic compounds (VOCs), H2, and CO2, which are comparable to or even better than the best results reported to date in these applications. To the best of our knowledge, this is the first synthesis of ultrasmall carbon nanospheres with uniform tunable sizes and superior performances for these applications by the emulsion polymerization strategy.Item Polycyclopentene crystal-decorated carbon nanotubes by convenient large-scale in situ polymerization and their lotus leaf-like superhydrophobic films.(2016-12-22) Ye, Zhibin; Xu, Lixin; Huang, Lingqi; Meng, Nan; Shu, Yang; Gu, ZhiyongIn situ Pd-catalyzed cyclopentene polymerization in the presence of multi-walled carbon nanotubes (MWCNTs) is demonstrated to effectively render, on a large scale, polycyclopentene-crystal-decorated MWCNTs. Controlling the catalyst loading and/or time in the polymerization offers a convenient tuning of the polymer content and the morphology of the decorated MWCNTs. Appealingly, films made of the decorated carbon nanotubes through simple vacuum filtration show the characteristic lotus-leaf-like superhydrophobicity with high water contact angle (>150°), low contact angle hysteresis (<10°), and low water adhesion, while being electrically conductive. This is the first demonstration of the direct fabrication of lotus-leaf-like superhydrophobic films with solution-grown polymer-crystal-decorated carbon nanotube.Item Modification of cellulose nanocrystals with quaternary ammonium-containing hyperbranched polyethylene ionomers by ionic assembly(American Chemical Society, 2016-07-25) Huang, Lingqi; Ye, Zhibin; Berry, RichardIn this article, we demonstrate the first surface modification of cellulose nanocrystals (CNCs) with quaternary ammonium-containing ionomers by ionic binding of their positively charged ammonium ions onto the negatively charged surface of CNCs. A range of hyperbranched polyethylene ionomers (I1–I6) having different ionic content (0.2–2.3 mol %) has been designed and employed for this purpose. The simple dropwise addition and mixing of the aqueous dispersion of CNCs with the ionomer solution in tetrahydrofuran (THF) conveniently renders the ionomer-modified CNCs (mCNC1–mCNC6). The presence of adsorbed ionomers on the modified CNCs is confirmed with spectroscopic and X-ray diffraction evidence and quantified through thermogravimetric analysis. The effects of the ionomer to CNC feed mass ratio and the ionomers of different ionic content on the modification have been examined. A study on the morphology of the modified CNCs by atomic force microscopy discloses the occurrence of side-to-side and/or end-to-end assembly of the CNC rods due to the “cross-linking” or bridging effects of the multidentate ionomers. Because of the hydrophobic hyperbranched polyethylene segments in the adsorbed ionomers, the modified CNCs can be dispersed in nonpolar or low-polarity organic solvents (such as THF, toluene, and chloroform). In particular, the THF dispersions of modified CNCs prepared with ionomers having ionic content ≥0.7 mol % (I3–I6) behave as thixotropic organo-gels at concentrations ≥40 mg mL–1. Further, the modified CNCs better disperse than unmodified CNCs in a hydrophobic ethylene–olefin copolymer (EOC) elastomer matrix and show better thermal stability than a surfactant-modified CNC sample. Tensile testing confirms that the EOC composites, filled with the ionomer-modified CNCs, are significantly reinforced with a tensile modulus nearly doubled that of neat EOC, and they demonstrate better elongation at break relative to those filled with unmodified CNCs or surfactant-modified CNCs.Item Efficient, robust surface functionalization and stabilization of gold nanorods with quaternary ammonium-containing ionomers as multidentate macromolecular ligands(2016-04-25) Dong, Zhongmin; Xiang, Peng; Huang, Lingqi; Ye, ZhibinSurface functionalization of gold nanorods (GNRs) is critical to their applications in various fields. While there are several existing strategies, we report in this article a new general strategy for the surface functionalization of GNRs with quaternary ammonium-containing ionomers as a novel class of multidentate macromolecular surface ligands. A range of tetralkylammoniumcontaining hyperbranched polyethylene- and linear poly(n-butyl acrylate)-based ionomers has been specifically designed and employed in the strategy. Acting as multidentate macromolecular analogues of cetyltrimethylammonium bromide (CTAB), the ionomers have been demonstrated to bind onto the GNR surface by displacing the surface-bound CTAB species via ligand exchange to render CTAB-free ionomer-modified GNRs. By properly designing the enabling ionomers, we have shown that the modified GNRs can be endowed with some desired properties, such as excellent dispersibility in various organic solvents, robust stability under multiple rounds (up to 12 investigated) of high-speed centrifugation in organic solvents, amphiphilicity with dispersibility in both aqueous and organic media, fluorescence, and capability in carrying hydrophobic guest species. This strategy thus provides potential new ways for the construction of novel multifunctional GNR nanocomposites.