Activated carbons as catalytic support for Cu nanoparticles

There are a wide range of catalytic applications for Cu-based nanoparticles materials, since Cu is an abundant and inexpensive metal and Cu nanoparticles possess unusual electrical, thermal and optical properties. The possible modification of the chemical and physical properties of these nanoparticles using different synthetic strategies and conditions and/or via postsynthetic chemical treatments has been largely responsible for the rapid growth of interest in these nanomaterials and their applications in catalysis. A previous work have explored the possibilities of SBA-15 (1,2) as support for Cu nanoparticles. In the present contribution, those results will be compared with the use of a carbon material as support, since activated carbon present many advantages with respect SBA, as the high surface area.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech

Optical Excitation of a Nanoparticle Cu/p-NiO Photocathode Improves Reaction Selectivity for CO₂ Reduction in Aqueous Electrolytes

We report the light-induced modification of catalytic selectivity for photoelectrochemical CO₂ reduction in aqueous media using copper (Cu) nanoparticles dispersed onto p-type nickel oxide (p-NiO) photocathodes. Optical excitation of Cu nanoparticles generates hot electrons available for driving CO₂ reduction on the Cu surface, while charge separation is accomplished by hot-hole injection from the Cu nanoparticles into the underlying p-NiO support. Photoelectrochemical studies demonstrate that optical excitation of plasmonic Cu/p-NiO photocathodes imparts increased selectivity for CO₂ reduction over hydrogen evolution in aqueous electrolytes. Specifically, we observed that plasmon-driven CO₂ reduction increased the production of carbon monoxide and formate, while simultaneously reducing the evolution of hydrogen. Our results demonstrate an optical route toward steering the selectivity of artificial photosynthetic systems with plasmon-driven photocathodes for photoelectrochemical CO₂ reduction in aqueous media

Pharmacokinetics and tumor dynamics of the nanoparticle IT-101 from PET imaging and tumor histological measurements

IT-101, a cyclodextrin polymer-based nanoparticle containing camptothecin, is in clinical development for the treatment of cancer. Multiorgan pharmacokinetics and accumulation in tumor tissue of IT-101 is investigated by using PET. IT-101 is modified through the attachment of a 1,4,7,10-tetraazacyclododecane-1,4,7-Tris-acetic acid ligand to bind ^(64)Cu^(2+). This modification does not affect the particle size and minimally affects the surface charge of the resulting nanoparticles. PET data from ^(64)Cu-labeled IT-101 are used to quantify the in vivo biodistribution in mice bearing Neuro2A s.c. tumors. The ^(64)Cu-labeled IT-101 displays a biphasic plasma elimination. Approximately 8% of the injected dose is rapidly cleared as a low-molecular-weight fraction through the kidneys. The remaining material circulates in plasma with a terminal half-life of 13.3 h. Steadily increasing concentrations, up to 11% injected dose per cm^3, are observed in the tumor over 24 h, higher than any other tissue at that time. A 3-compartment model is used to determine vascular permeability and nanoparticle retention in tumors, and is able to accurately represent the experimental data. The calculated tumor vascular permeability indicates that the majority of nanoparticles stay intact in circulation and do not disassemble into individual polymer strands. A key assumption to modeling the tumor dynamics is that there is a “sink” for the nanoparticles within the tumor. Histological measurements using confocal microscopy show that IT-101 localizes within tumor cells and provides the sink in the tumor for the nanoparticles

Cu,Zn,Al layered double hydroxides as precursors for copper catalysts in methanol steam reforming – pH-controlled synthesis by microemulsion technique

By co-precipitation inside microemulsion droplets a Cu-based catalyst precursor was prepared with a Cu:Zn:Al ratio of 50:17:33. A pH-controlled synthesis was applied by simultaneous dosing of metal solution and precipitation agent. This technique allows for continuous operation of the synthesis and enables easy and feasible up-scaling. For comparison conventional co-precipitation was applied with the same composition. Both techniques resulted in phase pure layered double hydroxide precursors and finally (after calcination and reduction) in small Cu nanoparticles (8 nm) and ZnAl2O4. By applying the microemulsion technique smaller Cu/ZnAl2O4 aggregates with less embedded Cu particles were obtained. The microemulsion product exhibited a higher BET and specific Cu surface area and also a higher absolute catalytic activity in methanol steam reforming. However, the Cu surface area-normalized, intrinsic activity was lower. This observation was related to differences in interactions of Cu metal and oxide phase

A one-step Cu/ZnO Quasi-Homogeneous Catalyst for DME Production from Syn-gas

Colloidal Cu/ZnO nanoparticles combine with γ-Al2O3 to form promising hybrid catalysts for the direct synthesis of dimethyl ether (DME) in liquid phase, showing high activity, selectivity and stability.</p

Bimetallic Au-Cu Nanoparticles Anchored Reduced Graphene Oxide as Efficient Catalyst for Reduction of Nitro Aromatic Compounds

In the present work an efficient nanocomposite Au-Cu/rGO has been synthesised by decorating Au-Cu bimetallic nanoparticles on reduced graphene oxide surface via co-reduction method. The nanocomposite was characterized using X-ray diffraction (XRD), Field-emission Scanning electron microscopy (FE-SEM), Energy dispersive X-ray spectroscopy (EDS), Transmission electron microscopy (TEM) and UV-Visible spectroscopy. The FE-SEM and TEM images demonstrate the uniform distribution of the Au-Cu bimetallic nanoparticles on the GO surface and transmission electron microscopy (TEM) confirms an average particle size of 6-8 nm. The Au-Cu/rGO nanocomposite has been found to be an extremely efficient catalyst for the reduction of nitroaromatic compounds into nitroamine compounds. The Au-Cu/rGO nanocomposites exhibited synergistically more superior catalytic efficiency compared to monometallic Au nanoparticles doped reduced graphene oxide and monometallic Cu nanoparticles doped reduced graphene oxide. The reaction conditions were optimized by changing different parameters such as catalyst dose and reducing agent concentratio