Enviromental Barriers and Pain Catastrophizing

For people with impairments, both the environment and experience of pain can limit participation, which is important to one’s quality of life. As a result, the perception of pain and impact of environmental barriers can be important factors in determining quality of life for these individuals. Little research has examined environmental barriers and pain catastrophizing. This correlational study examined the relationship between environmental barriers (e.g., weather, light, accessibility) and pain catastrophizing (i.e., one’s thoughts about their pain intensity). Surveys were collected from 272 randomly selected individuals ages 18-64, who were residing in a small Western US city. These individuals experience pain in conjunction with some form of physical disability. In this study there were 107 male and 165 female participants with an average age of 50.7 years old. The Pain Catastrophizing Scale has been used to assess psychological suffering in response to pain. The Survey of Participation and Receptivity in Communities (SPARC) has been used to assess the frequency and magnitude of barriers experienced by people with various impairments. I hypothesized that frequency of environmental barriers would predict pain catastrophizing because people who are sensitive to pain may be sensitive to their environment. Such a generalized sensitivity across pain and barrier domains may help us understand important factors that affect an individual’s participation in the community. The Statistical Package for the Social Sciences (SPSS 20.0) was used to complete multiple regression analyses. Elements of pain catastrophizing and the frequency and magnitude of barriers were compared. This investigation of environmental barriers and pain catastrophizing may advance our understanding of pain and participation that could be used for developing interventions for treating chronic pain and to improve the quality of life for people who have impairments. Keywords: environmental barriers, pain catastrophizin

Gedanken über Protestantismus und Tradition

Digiteeritud Euroopa Regionaalarengu Fondi rahastusel, projekti "Eesti teadus- ja õppekirjandus" (2014-2020.12.03.21-0848) raames.https://www.ester.ee/record=b1667005*es

Die Verfassungsentwicklung Estlands

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Auf verlorenem Posten : Schauspiel in 2 Acten

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The model case of an oxygen storage catalyst - non-stoichiometry, point defects and electrical conductivity of single crystalline CeO2-ZrO2-Y2O3 solid solutions

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich.This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.The ternary solid solution CeO2–ZrO2 is known for its superior performance as an oxygen storage catalyst in exhaust gas catalysis (e.g. TWC), although the defect chemical background of these outstanding properties is not fully understood quantitatively. Here, a comprehensive experimental study is reported regarding defects and defect-related transport properties of cubic stabilized single crystalline (CexZr1−x)0.8Y0.2O1.9−δ (0 ≤ x ≤ 1) solid solutions as a model system for CeO2–ZrO2. The constant fraction of yttria was chosen in order to fix a defined concentration of oxygen vacancies and to stabilize the cubic fluorite-type lattice for all Ce/Zr ratios. Measurements of the total electrical conductivity, the partial electronic conductivity, the ionic transference number and the non-stoichiometry (oxygen deficiency, oxygen storage capacity) were performed in the oxygen partial pressure range −25 < lg pO2/bar < 0 and for temperatures between 500 °C and 750 °C. The total conductivity at low pO2 is dominated by electronic transport. A strong deviation from the widely accepted ideal solution based point defect model was observed. An extended point defect model was developed using defect activities rather than concentrations in order to describe the point defect reactions in CeO2–ZrO2–Y2O3 properly. It served to obtain good quantitative agreement with the measured data. By a combination of values for non-stoichiometries and for electronic conductivities, the electron mobility could be calculated as a function of pO2, ranging between 10−2 cm2 V−1 s−1 and 10−5 cm2 V−1 s−1. Finally, the origin of the high oxygen storage capacity and superior catalytic promotion performance at a specific ratio of n(Ce)/n(Zr) ≈ 1 was attributed to two main factors: (1) a strongly enhanced electronic conductivity in the high and medium pO2 range qualifies the material to be a good mixed conductor, which is essential for a fast oxygen exchange and (2) the equilibrium constant for the reduction exhibits a maximum, which means that the reduction is thermodynamically most favoured just at this composition

Intermetallic Fe6Ge5Fe_{6} Ge_{5} formation and decay of a core–shell structure during the oxygen evolution reaction

Herein, we report on intermetallic iron germanide ($Fe_{6} Ge_{5}$) as a novel oxygen evolution reaction (OER) precatalyst with a Tafel slope of 32 mV $dec^{−1}$ and an overpotential of 272 mV at 100 mA $cm^{−2}$ in alkaline media. Furthermore, we uncover the in situ formation of a core–shell like structure that slowly collapses under OER conditions

Lithium metal penetration induced by electrodeposition through solid electrolytes: Example in single-crystal Li6La3ZrTaO12 garnet

Solid electrolytes potentially enable rechargeable batteries with lithium metal anodes possessing higher energy densities than today’s lithium ion batteries. To do so the solid electrolyte must suppress instabilities that lead to poor coulombic efficiency and short circuits. In this work, lithium electrodeposition was performed on single-crystal Li6La3ZrTaO12 garnets to investigate factors governing lithium penetration through brittle electrolytes. In single crystals, grain boundaries are excluded as paths for lithium metal propagation. Vickers microindentation was used to introduce surface flaws of known size. However, operando optical microscopy revealed that lithium metal penetration propagates preferentially from a different, second class of flaws. At the perimeter of surface current collectors smaller in size than the lithium source electrode, an enhanced electrodeposition current density causes lithium filled cracks to initiate and grow to penetration, even when large Vickers defects are in proximity. Modeling the electric field distribution in the experimental cell revealed that a 5-fold enhancement in field occurs within 10 micrometers of the electrode edge and generates high local electrochemomechanical stress. This may determine the initiation sites for lithium propagation, overriding the presence of larger defects elsewhere

Ion dynamics in Al-Stabilized Li7La3Zr2O12 single crystals – Macroscopic transport and the elementary steps of ion hopping

Li7La3Zr2O12 (LLZO) garnet-type ceramics are considered as very promising candidates for solid electrolytes and have been extensively studied in the past few years. Several studies report on an increase in ionic conductivity by doping with ions, such as Al3+ and Ga3+, to stabilize the cubic modification of LLZO. Unfortunately, so far ion dynamics have mainly been studied using powdered samples. Such studies may suffer from chemical heterogeneities concerning Al distribution. Here, we took advantage of Al-stabilized LLZO single crystals to throw light on the elementary steps of ion hopping. We used 7Li nuclear magnetic resonance (NMR) spin-lattice relaxation measurements and conductivity spectroscopy to probe dynamic parameters from both a microscopic and macroscopic point of view. At 293 K the total conductivity turned out to be 0.082 mS cm−1, which is remarkably good for LLZO exhibiting an Al-content of only 0.37 wt%. Most importantly, 7Li NMR spin-lock transients revealed two overlapping diffusion-induced processes. Overall, activation energies from spin-lock NMR excellently agree with that from conductivity measurements; both techniques yield values around 0.36 eV. The corresponding diffusion coefficients deduced from NMR and conductivity measurements almost coincide. The magnetic spin fluctuations sensed by NMR provide an in-depth look at the elementary jump processes, which can barely be revealed by macroscopic impedance spectroscopy providing average values. In particular, we were able to precisely measure the local hopping barrier (0.20 eV) characterizing forward-backward jumps between the sites 24d and 96h. © 2019 The Author(s

Structure and dynamics of the fast lithium ion conductor "li 7La3Zr2O12"

The solid lithium-ion electrolyte "Li7La3Zr 2O12" (LLZO) with a garnet-type structure has been prepared in the cubic and tetragonal modification following conventional ceramic syntheses routes. Without aluminium doping tetragonal LLZO was obtained, which shows a two orders of magnitude lower room temperature conductivity than the cubic modification. Small concentrations of Al in the order of 1 wt% were sufficient to stabilize the cubic phase, which is known as a fast lithium-ion conductor. The structure and ion dynamics of Al-doped cubic LLZO were studied by impedance spectroscopy, dc conductivity measurements, 6Li and 7Li NMR, XRD, neutron powder diffraction, and TEM precession electron diffraction. From the results we conclude that aluminium is incorporated in the garnet lattice on the tetrahedral 24d Li site, thus stabilizing the cubic LLZO modification. Simulations based on diffraction data show that even at the low temperature of 4 K the Li ions are blurred over various crystallographic sites. This strong Li ion disorder in cubic Al-stabilized LLZO contributes to the high conductivity observed. The Li jump rates and the activation energy probed by NMR are in very good agreement with the transport parameters obtained from electrical conductivity measurements. The activation energy Ea characterizing long-range ion transport in the Al-stabilized cubic LLZO amounts to 0.34 eV. Total electric conductivities determined by ac impedance and a four point dc technique also agree very well and range from 1 × 10-4 Scm-1 to 4 × 10-4 Scm-1 depending on the Al content of the samples. The room temperature conductivity of Al-free tetragonal LLZO is about two orders of magnitude lower (2 × 10 -6 Scm-1, Ea = 0.49 eV activation energy). The electronic partial conductivity of cubic LLZO was measured using the Hebb-Wagner polarization technique. The electronic transference number te- is of the order of 10-7. Thus, cubic LLZO is an almost exclusive lithium ion conductor at ambient temperature. © the Owner Societies 2011