883 research outputs found
Impact of Education on Grandparentsâ Actions in Raising Grandchildren
Grandparents raising grandchildren represent a population of adults who confront complex interpersonal and environmental challenges. The intent of this case study was to gather and interpret evaluative data to better understand the impact of a 1-day community education program for grandparents who raise their grandchildren. Extension\u27s philosophy of systematic program evaluation to improve supports for families and communities furnished the framework for the project. Elements felt to be essential for a well-designed, 1-day grandparent education program have been extracted from past evaluation cycles and offered here as recommendations
Dual-plate gold-gold microtrench electrodes for generator-collector voltammetry without supporting electrolyte
A gold-gold dual-plate microtrench electrode system based on two oppositely placed gold surfaces with 5Â mm length, 17Â ÎŒm average depth, and 6Â ÎŒm inter-electrode gap is employed in generator-collector configuration in a four-electrode cell (counter electrode, reference electrode, and two independent working electrodes denoted âgeneratorâ â with scanning potential â and âcollectorâ â with fixed potential). The dual-plate microtrench electrodes were investigated for (i) the reduction of Ru(NH3)6 3+, (ii) the oxidation of ferrocenemethanol, and (iii) the oxidation of iodide in aqueous media, all as a function of supporting electrolyte concentration. It is shown that due to the inter-electrode feedback character of the generator-collector currents, well-defined steady state sensor responses are obtained for the collector electrode even in the absence of added electrolyte. The variation in the mass transport limited steady state current (measured at the collector electrode) with addition/removal of supporting electrolyte remains low (compared to unexpectedly stronger effects caused by the switch between reduction and oxidation conditions at the collector electrode). Microtrench electrode systems are suggested for sensing applications without/with varying levels of supporting electrolyte.</p
Effects of dissolved gases on partial anodic passivation phenomena at copper microelectrodes immersed in aqueous NaCl
Anodic passivation for copper exposed to aqueous NaCl (model seawater) is rate limited by diffusion of a poorly soluble Cu(I) chloro species. As a result, a protective layer of CuCl forms on copper metal (with approx. 1 ÎŒm thickness) that is then put under strain at more positive applied potentials with explosive events causing current spikes and particulate product expulsion. In this report, the mechanism for this explosive film rupture and particle expulsion process is shown to occur (i) in the absence of underlying anodic gas evolution, and (ii) linked to the presence/nature of gaseous solutes. The film rupture event is proposed to be fundamentally dependent on gas bubble nucleation (triggered by the release of interfacial stress) with surface tension effects by dissolved gases affecting the current spike pattern. Oxygen O2, hydrogen H2, and helium He suppress current spikes and behave differently to argon Ar, nitrogen N2, and carbon dioxide CO2, which considerably enhance current spikes. Vacuum-degassing the electrolyte solution results in behaviour very similar to that observed in the presence of helium. The overall corrosion rate for copper microelectrodes is compared and parameters linked to passivation and corrosion processes are discussed.</p
Effects of dissolved gases on partial anodic passivation phenomena at copper microelectrodes immersed in aqueous NaCl
Generator-collector voltammetry at dual-plate gold-gold microtrench electrodes as diagnostic tool in ionic liquids
Ionic liquids provide high viscosity solvent environments with interesting voltammetric characteristics and new electrochemical mechanisms. Here, a gold-gold dual-plate microtrench electrode is employed in generator-collector mode to enhance viscosity-limited currents in ionic liquids due to fast feedback within small inter-electrode gaps (5ÎŒm inter-electrode gap, 27ÎŒm microtrench depth) and to provide a mechanistic diagnosis tool. Three redox systems in the ionic liquid BMIm+BF4- are investigated: (i) ferrocene oxidation, (ii) oxygen reduction, and (iii) 2-phenyl-naphthyl-1,4-dione reduction. Both transient and steady state voltammetric responses are compared. Asymmetric diffusion processes, reaction intermediates, and solubility changes in the ionic liquid are revealed.</p
Switching ionic diode states with proton binding into intrinsically microporous polyamine films (PIM-EA-TB) immersed in ethanol
Tuning and Coupling Irreversible Electroosmotic Water Flow in Ionic Diodes:Methylation of an Intrinsically Microporous Polyamine (PIM-EA-TB)
Electrochemical reactivity of TiO2 nanoparticles adsorbed onto boron-doped diamond
TiO2 (anatase) nanoparticles of ca. 6â10 nm diameter are adsorbed from acidic aqueous solution onto polycrystalline industrially polished boron-doped diamond electrode surfaces. After immobilisation at the electrode surface, TiO2 nanoparticles are imaged in vacuum by electron microscopy (FEGSEM) and when immersed in a liquid film of aqueous 12 M LiCl by in situ scanning tunnelling microscopy (STM). Mono-layer films of TiO2 particles are studied voltammetrically in different electrolyte media.
Boron-doped diamond as an inert substrate material allows the reduction of TiO2 particles in phosphate buffer solution to be studied and two distinct steps in the reductionâprotonation process are identified: (i) a broad reduction signal associated with the binding of an outer layer of protons and (ii) a sharper second reduction signal associated with the binding of an inner (or deeper) layer of protons. Voltammetric experiments in aqueous 0.1 M NaClO4 with variable amounts of HClO4 suggest that the reduction of TiO2 particles is consistent with the formation of Ti(III) surface sites and accompanied by the adsorption of protons. Saturation occurs and the total amount of surface sites can be determined. Preliminary data for electron transfer processes at the reduced TiO2 surface such as the dihydrogen evolution process and the two-electronâtwo-proton reduction of maleic acid to succinic acid are discussed
Hypoxia induces no change in cutaneous thresholds for warmth and cold sensation
Hypoxia can affect perception of temperature stimuli by impeding thermoregulation at a neural level. Whether this impact on the thermoregulatory response is solely due to affected thermoregulation is not clear, since reaction time may also be affected by hypoxia. Therefore, we studied the effect of hypoxia on thermal perception thresholds for warmth and cold. Thermal perception thresholds were determined in 11 healthy overweight adult males using two methods for small nerve fibre functioning: a reaction-time inclusive method of limits (MLI) and a reaction time exclusive method of levels (MLE). The subjects were measured under normoxic and hypoxic conditions using a cross-over design. Before the thermal threshold tests under hypoxic conditions were conducted, the subjects were acclimatized by staying 14 days overnight (8 h) in a hypoxic tent system (Colorado Altitude Training: 4,000 m). For normoxic measurements the same subjects were not acclimatized, but were used to sleep in the same tent system. Measurements were performed in the early morning in the tent. Normoxic MLI cold sensation threshold decreased significantly from 30.3 ± 0.4 (mean ± SD) to 29.9 ± 0.7°C when exposed to hypoxia (P < 0.05). Similarly, mean normoxic MLI warm sensation threshold increased from 34.0 ± 0.9 to 34.5 ± 1.1°C (P < 0.05). MLE measured threshold for cutaneous cold sensation was 31.4 ± 0.4 and 31.2 ± 0.9°C under respectively normoxic and hypoxic conditions (P > 0.05). Neither was there a significant change in MLE warm threshold comparing normoxic (32.8 ± 0.9°C) with hypoxic condition (32.9 ± 1.0°C) (P > 0.05). Exposure to normobaric hypoxia induces slowing of neural activity in the sensor-to-effector pathway and does not affect cutaneous sensation threshold for either warmth or cold detection
Hydrogen Peroxide Versus Hydrogen Generation at Bipolar Pd/Au Nano-catalysts Grown into an Intrinsically Microporous Polyamine (PIM-EA-TB)
Binding of PdCl42â into the polymer of intrinsic microporosity PIM-EA-TB (on a Nylon mesh substrate) followed by borohydride reduction leads to uncapped Pd(0) nano-catalysts with typically 3.2â±â0.2 nm diameter embedded within the microporous polymer host structure. Spontaneous reaction of Pd(0) with formic acid and oxygen is shown to result in the competing formation of (i) hydrogen peroxide (at low formic acid concentration in air; with optimum H2O2 yield at 2 mM HCOOH), (ii) water, or (iii) hydrogen (at higher formic acid concentration or under argon). Next, a spontaneous electroless gold deposition process is employed to attach gold (typically 10- to 35-nm diameter) to the nano-palladium in PIM-EA-TB to give an order of magnitude enhanced production of H2O2 with high yields even at higher HCOOH concentration (suppressing hydrogen evolution). Pd and Au work hand-in-hand as bipolar electrocatalysts. A Clark probe method is developed to assess the catalyst efficiency (based on competing oxygen removal and hydrogen production) and a mass spectrometry method is developed to monitor/optimise the rate of production of hydrogen peroxide. Heterogenised Pd/Au@PIM-EA-TB catalysts are effective and allow easy catalyst recovery and reuse for hydrogen peroxide production
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