Super Pill is Less Effective than an Ordinary Mint in Altering Subjective Psychological Feeling States within a Few Minutes

Expectations shape human behavior. Initial drug use might be associated with information-based expectations. In this study, we presumed that changes in affect and perceived physical wellbeing will be stronger after receiving an active placebo (Tic Tac mint; n = 40), than a pure placebo (inert pill; n = 40) given as a mood-enhancing super pill. After baseline measures, participants completed a treatment-expectancy scale, ingested the mint/super pill, and attended to the effects over 3-minutes. Subsequently, they completed again the psychological tests. Expectancy scores were positive and did not differ between the groups. The pure placebo group increased in physical wellbeing but less than the active placebo group, which also showed an increase in positive affect. Negative affect decreased in both groups. The Tic Tac produced greater affective changes than the pure placebo. Since these are new findings on the ultra-short placebo effects on affect, the results might have relevance for drug-use studies

Fire patterns in central semiarid Argentina.

Wildfires can cause severe impacts on the terrestrial ecosystems depending on their frequency and behavior. We studied the environmental factors influencing the spatial and temporal distribution of fires, their size and duration in the central semiarid Argentina. We identified fires using MODIS satellite data and we analyzed their association with climate and land cover/use patterns. Spatial and temporal fire patterns varied between eastern, central and western regions according to the presence of agriculture, shrublands and water deficits, respectively. The frequency and behavior of fires also varied temporally with water conditions. Years with low effective precipitations were characterized by an important hotspot density and fire number, as well as the months preceded by two months with low effective precipitation (r 2: 0.42; p < 0.0001). We observed a spatial delay of fires in a northeast-southwest sense, related to the delay of the spring beginning (r 2: 0.7594; p < 0.0001). The mean fire sizes and duration varied significantly among vegetation types (F: 10.76, p < 0.0001 and F: 3.703, p < 0.01). Fires were bigger in shrublands and longer in shrublands or forests regarding agricultural areas or degraded areas (F: 16.0, p < 0.0001). The results obtained would be useful to prevent/control fires and to preserve natural resources and human communities.Fil: Fischer, M. A.. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación de Recursos Naturales. Instituto de Clima y Agua; ArgentinaFil: Di Bella, Carlos Marcelo. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación de Recursos Naturales. Instituto de Clima y Agua; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Jobbágy, Esteban Gabriel. Universidad Nacional de San Luis; Argentin

Mesoporous Microspheres of Nickel-based Layered Hydroxides by Aerosol-Assisted Self-Assembly using Crystalline Nano-Building Blocks.

Structural control in micro- and nanometer scale is necessary to design highly functional materials. Crystalline mesoporous microspheres are expected to improve electrochemical, catalytic, and adsorption performances. In this study, we focused on the preparation of templated mesoporous microspheres of nickel-based layered hydroxides by using pre-crystallized nano-building blocks (NBBs). Layered nickel hydroxide nanoparticles were prepared through an epoxide-mediated alkalinization process and used as NBBs to construct microspheres. The spherical particles in micrometer scale were synthesized by an aerosol-assisted assembly of the NBBs dispersed in a solvent, in the presence of supramolecular templates. It was found that controlling the crystallization as well as the surface philicity permits to yield the NBB with an adequately small size and interparticle interactions that generate self-assembled mesoporous microspheres akin to those obtained in NBB-based mesoporous thin films. The preparation technique demonstrated here is highly versatile; templated mesoporous microspheres with various chemical compositions of nickel-based layered double hydroxides were successfully obtained.The present work was partially supported by JSPS KAKENHI, JSPS bilateral program, LNLS proposal SAXS1 18927, ANPCyT (PICT 2012-2087 and 2015-3526), UBACyT (20020130100610BA), Hitachi Metals Materials Science Foundation, The Sumitomo Foundation, and Izumi Science and Technology Foundation

Microparticles with hetero-nanointerfaces: controlled assembly of cobalt hydroxide and nickel hydroxide nanoclusters towards improved electrochemical functions

The ultimate control of the interfaces of nanocomposite materials is essential to tailor and improve their physical/chemical properties in applications such as catalysis, or energy storage or production. Fabrication and co-assembly of a variety of nanostructured colloids is a promising way to design the interface of materials in nano-scale toward high functionality. In this study, we demonstrate a synthesis of colloids of nanocluster-sized (~ 2 nm) cobalt and nickel hydroxides and their assembly into microparticles that present hetero-nanointerfaces. Electrochemical properties were investigated to elucidate the effect of the hetero-nanointerface. Microparticles with hetero nanostructures composed of cobalt and nickel hydroxide nanoclusters revealed improved mass specific capacity (91.4 mAh/g) compared with respective microparticles with homo-nanointerface (cobalt hydroxide; 15.8 mAh/g: nickel hydroxide; 64.4 mAh/g). Further investigation suggests that the introduced hetero-nanointerface leads to lower charge transfer resistance and to improved electrochemical properties. The synthetic concept demonstrated here is expected to create unique hetero-nanointerfaces for various materials with wide-range of chemical composition towards improved and novel functionalities.The present work is partially supported by JSPS KAKENHI, LNLS proposal SAXS1 18927, ANPCyT (PICT 2087), UBACyT (20020130100610BA), Izumi Science and Technology Foundation (H29-J-130) and the Foundation for the Promotion of Ion Engineering

Halide-mediated Modification of magnetism and electronic structure of α-Co (II) hydroxides: synthesis, characterization, and DFT+ U simulations

The present study introduces a comprehensive exploration in terms of physicochemical characterization and calculations based on density functional theory with Hubbard's correction (DFT+U) of the whole family of α-Co(II) hydroxyhalide (F, Cl, Br, I). These samples were synthesized at room temperature by employing a one-pot approach based on the epoxide route. A thorough characterization (powder X-ray diffraction, X-ray photoelectron spectroscopy, thermogravimetric analysis/mass spectroscopy, and magnetic and conductivity measurements) corroborated by simulation is presented that analyzes the structural, magnetic, and electronic aspects. Beyond the inherent tendency of intercalated anions to modify the interlayer distance, the halide's nature has a marked effect on several aspects. Such as the modulation of the CoOh to CoTd ratio, as well as the inherent tendency towards dehydration and irreversible decomposition. Whereas the magnetic behavior is strongly correlated with the CoTd amount reflected in the presence of glassy behavior with high magnetic disorder, the electrical properties depend mainly on the nature of the halide. The computed electronic structures suggest that the CoTd molar fraction exerts a minor effect on the inherent conductivity of the phases. However, the band gap of the solid turns out to be significantly dependent on the nature of the incorporated halide, governed by ligand to metal charge transfer, which minimizes the gap as the anionic radius becomes larger. Conductivity measurements of pressed pellets confirm this trend. To the best of our knowledge, this is the first report on the magnetic and electrical properties of α-Co(II) hydroxyhalides validated with in silico descriptions, opening the gate for the rational design of layered hydroxylated phases with tunable electrical, optical, and magnetic properties

Highly Ordered Mesoporous Hydroxide Thin Films through Self-Assembly of Size-Tailored Nano-Building Blocks: A Theoretical- Experimental Approach

Mesoporous crystalline (hydr)oxides of low-valence metal ions (M(II) and M(III)) are highly demanded in the context of various applications. In this study, we demonstrate key factors to the successful formation of ordered mesoporous films through the Assembly of Nano-Building Block (ANBB) approach using a colloidal solution of crystalline M(OH)2 (M = Mn, Fe, Co, Ni, and Cu). The colloidal system of α-Ni(OH)2 is presented in-depth as a typical example. Crystal growth and aggregation kinetics of the NBB were tuned by synthetic parameters. Nanometer-sized NBBs of tailored size between oligomer scale to over 20 nm were obtained. The films prepared from α-Ni(OH)2 NBBs with a diameter of ≤ 7.5 nm showed ordered mesostructures through evaporation-induced self-assembly in the presence of supramolecular templates. Coarse-grained simulation suggests that there is a threshold diameter of NBB toward the formation of wellordered mesostructures. It was found that, as well as limiting the diameter of NBB, inhibition of an aggregation of NBBs by using coordinative additives or diluting the NBB colloidal solution were essential to control the assembly of NBBs and templates into the ordered mesostructures. The results obtained here open up the synthesis of ordered mesoporous materials with a crystalline wall of variety of chemical compositions containing low-valence metal elements.The present work was partially supported by JSPS KAKENHI, JSPS bilateral program, ABTLuS (LNLS proposal SAXS1 18927), ANPCyT (PICT 2014-3687 and 2015-3526), UBACyT (20020130100610BA), The Sumitomo Foundation, Izumi Science and Technology Foundation and Deutsche Forschungsgemeinschaft-CONICET under grant Mu1674/15-1