Impedance tube measurements on the denorms round robin test material samples

The DENORMS Round Robin Test aims to study and improve the techniques used to determine the sound absorption coefficient of materials. Within this framework, samples taken from the same batch have been tested in both reverberation room and impedance tube. The latter technique presents some challenges in that the results may strongly depend on the specimen preparation and set-up. The purpose of this paper is to present the results obtained in custom-made impedance tube for the RRT set of materials. The tests have been carried out using a four-microphone impedance tube, according to the method outlined in the ASTM E2611-09 standard. The results obtained for the different parameters provided by the test, in particular the sound absorption coefficient and the sound transmission loss, are taken into account and discussed

Principles at the basis of the denorms round robin test on the low frequency sound absorption measurements in reverberation rooms and impedance tube

In recent years low frequency measurements in building and room acoustics fields gained attention. Moreover the low frequency sound absorption coefficient (below 100 Hz) has always been difficult to determine and the results coming from different laboratories cannot always be compared. This paper describes the principles at the basis of the round robin test carried out in the framework of the DENORMS cost action (Designs for Noise Reducing Materials and Structures). The same samples have been measured in reverberation rooms and in impedance tube by the different laboratories participating to the Round Robin Test.status: accepte

The DENORMS Round Robin test: Measurement procedure and post-processing of time data

The DENORMS Round Robin Test (RRT) is intended to study and improve the techniques used for the determination of the sound absorption coefficient of materials, with particular focus on the low-frequency range and on measurements in reverberation rooms. It is well known that the main reason why it is difficult to extend the frequency range of interest below 100 Hz is the low modal density. The modal behavior of a room is dependent on its geometry and this is one of the reasons why a discrepancy of the results coming from different laboratories can be found even if the same material is tested. This paper describes the measurement procedure developed to allow uniform acquisition and post-processing of acoustic response data of laboratories participating in the RRT, with and without absorbing materials inside. The tests and the post-processing operations performed on the measured data are also discussed in the paper

Comparative study of the phase transition of Li1+xMn2-xO4 by anelastic spectroscopy and differential scanning calorimetry

Li1+xMn2xO4 is one of the most promising candidates as high performance cathode for lithium ion batteries. The stoichiometric compound is known to undergo a phase transition around room temperature, which has been widely studied and attributed either to Jahn–Teller effect or to charge ordering. For the applications it is important to suppress this phase transition, which lowers the electrochemical performances of the material. DSC measurements, which have been largely used in the literature to study the occurrence of the transformation, can detect a phase transition accompanied by latent heat only for x < 0.04. This fact has been generally accepted as a proof that the transformation is suppressed by doping. However, by using a technique extremely sensitive to rearrangements of atoms in the lattice, such as anelastic spectroscopy, we show that the phase transition persists up to x = 0.08, is shifted to lower temperatures, and changes its nature from first to higher order. The implications for the mechanism driving the transition and the similarities and differences with doped Fe3O4, which is the prototype of charge order transitions, are discussed

Differentiation of haploid and diploid fertilities in Gracilaria chilensis affect ploidy ratio

Background Algal isomorphic biphasic life cycles alternate between free-living diploid (tetrasporophytes) and haploid (dioicious gametophytes) phases and the hypotheses explaining their maintenance are still debated. Classic models state that conditional differentiation between phases is required for the evolutionary stability of biphasic life cycles while other authors proposed that the uneven ploidy abundances observed in the field are explained by their cytological differences in spore production. Results We monitored the state and fate of individuals of the red seaweed Gracilaria chilensis periodically for 3 years in five intertidal pools from two sites with distinct conditions. We tested for differentiation in fecundity and spore survival among the gametophyte males and females (haploids) and the tetrasporophytes (diploids). We tested for the influence of fecundity and spore survival on the observed uneven ploidy abundances in recruits. The probability of a frond becoming fecund was size-dependent, highest for the haploid males and lowest for the haploid females, with the diploids displaying intermediate probabilities. Fecund diploids released more tetraspores than carpospores released by the haploid females. Spore survival depended on ploidy and on the local density of co-habiting adult fronds. An advantage of diploid over haploid germlings was observed at very low and very high adult fronds densities. Conclusions Neither spore production nor spore survival determined the highly variable ploidy ratio within G. chilensis recruits. This result invalidates the hypothesis of natural cytological differences in spore production as the only driver of uneven field ploidy abundances in this species. Diploid spores (carpospores) survived better than haploid spores (tetraspores), especially in locations and time periods that were associated with the occurrence of strong biotic and abiotic stressors. We hypothesise that carpospore survival is higher due to support by their haploid female progenitors passing-on nutrients and chemical compounds improving survival under stressful conditions.AHE was supported by fellowships SFRH/BPD/63703/2009, SFRH/BPD/ 107878/2015 and UID/Multi/04326/2016 of the National Science Foundation FCT of Portugal.info:eu-repo/semantics/publishedVersio

Anomalous Lattice Vibrations of Single and Few-Layer MoS2

Molybdenum disulfide (MoS2) of single and few-layer thickness was exfoliated on SiO2/Si substrate and characterized by Raman spectroscopy. The number of S-Mo-S layers of the samples was independently determined by contact-mode atomic-force microscopy. Two Raman modes, E12g and A1g, exhibited sensitive thickness dependence, with the frequency of the former decreasing and that of the latter increasing with thickness. The results provide a convenient and reliable means for determining layer thickness with atomic-level precision. The opposite direction of the frequency shifts, which cannot be explained solely by van der Waals interlayer coupling, is attributed to Coulombic interactions and possible stacking-induced changes of the intralayer bonding. This work exemplifies the evolution of structural parameters in layered materials in changing from the 3-dimensional to the 2-dimensional regime.Comment: 14 pages, 4 figure

In Situ Ambient Pressure X-ray Photoelectron Spectroscopy Studies of Lithium-Oxygen Redox Reactions

The lack of fundamental understanding of the oxygen reduction and oxygen evolution in nonaqueous electrolytes significantly hinders the development of rechargeable lithium-air batteries. Here we employ a solid-state Li4+xTi5O12/LiPON/LixV2O5 cell and examine in situ the chemistry of Li-O2 reaction products on LixV2O5 as a function of applied voltage under ultra high vacuum (UHV) and at 500 mtorr of oxygen pressure using ambient pressure X-ray photoelectron spectroscopy (APXPS). Under UHV, lithium intercalated into LixV2O5 while molecular oxygen was reduced to form lithium peroxide on LixV2O5 in the presence of oxygen upon discharge. Interestingly, the oxidation of Li2O2 began at much lower overpotentials (~240 mV) than the charge overpotentials of conventional Li-O2 cells with aprotic electrolytes (~1000 mV). Our study provides the first evidence of reversible lithium peroxide formation and decomposition in situ on an oxide surface using a solid-state cell, and new insights into the reaction mechanism of Li-O2 chemistry.National Science Foundation (U.S.) (Materials Research Science and Engineering Center (MRSEC) Program, Award DMR-0819762)United States. Dept. of Energy (Assistant Secretary for Energy Efficiency and Renewable Energy, Office of FreedomCAR and Vehicle Technologies of the U. S. Department of Energy under contract no. DE-AC03-76SF00098)Lawrence Berkeley National LaboratoryUnited States. Dept. of Energy (Office of Basic Energy Sciences, Materials Sciences and Engineering

Multifunctional semi-interpenetrating polymer network-nanoencapsulated cathode materials for high-performance lithium-ion batteries

As a promising power source to boost up advent of next-generation ubiquitous era, high-energy density lithium-ion batteries with reliable electrochemical properties are urgently requested. Development of the advanced lithium ion-batteries, however, is staggering with thorny problems of performance deterioration and safety failures. This formidable challenge is highly concerned with electrochemical/thermal instability at electrode material-liquid electrolyte interface, in addition to structural/chemical deficiency of major cell components. Herein, as a new concept of surface engineering to address the abovementioned interfacial issue, multifunctional conformal nanoencapsulating layer based on semi-interpenetrating polymer network (semi-IPN) is presented. This unusual semi-IPN nanoencapsulating layer is composed of thermally-cured polyimide (PI) and polyvinyl pyrrolidone (PVP) bearing Lewis basic site. Owing to the combined effects of morphological uniqueness and chemical functionality (scavenging hydrofluoric acid that poses as a critical threat to trigger unwanted side reactions), the PI/PVP semi-IPN nanoencapsulated-cathode materials enable significant improvement in electrochemical performance and thermal stability of lithium-ion batteries.open

Conductive Cellulose Composites with Low Percolation Threshold for 3D Printed Electronics

We are reporting a 3D printable composite paste having strong thixotropic rheology. The composite has been designed and investigated with highly conductive silver nanowires. The optimized electrical percolation threshold from both simulation and experiment is shown from 0.7&thinsp;vol. % of silver nanowires which is significantly lower than other composites using conductive nano-materials. Reliable conductivity of 1.19&thinsp;×&thinsp;102&thinsp;S/cm has been achieved from the demonstrated 3D printable composite with 1.9&thinsp;vol. % loading of silver nanowires. Utilizing the high conductivity of the printable composites, 3D printing of designed battery electrode pastes is demonstrated. Rheology study shows superior printability of the electrode pastes aided by the cellulose\u27s strong thixotropic rheology. The designed anode, electrolyte, and cathode pastes are sequentially printed to form a three-layered lithium battery for the demonstration of a charging profile. This study opens opportunities of 3D printable conductive materials to create printed electronics with the next generation additive manufacturing process