Dataset associated with 'Synchrotron FTIR Mapping of Mineralization in a Microfluidic Device'

Fourier transform infrared micro-spectroscopy provides an effective means of performing rapid, non-destructive, and label-free analysis of specimens according to their vibrational modes. However, as water absorbs very strongly in the infrared region, analysis of aqueous solutions in transmission mode can suffer from problems with signal saturation. We here describe the fabrication of a novel microfluidic device that overcomes this problem. Devices with channel depths of just 3 µm were constructed from calcium fluoride using photolithography and hot embossing bonding, where calcium fluoride was selected due to its transparency in the IR region. The utility of this device was then demonstrated by employing it to follow the precipitation pathways of calcium sulfate and calcium carbonate using synchrotron FTIR micro-spectroscopy. Importantly, due to the high brightness provided by synchrotron radiation, and the fact that the reacting ions (HCO3- , CO32- and SO42-) and the different mineral polymorphs all have finger print spectra in the measured IR range, this method can be used to acquire time-resolved, hyperspectral maps of the mineral particles formed within the sample cell, and then study the interaction and evolution of particles. The data provide new insight into the formation pathway of a population of crystals in confined volumes, and demonstrate that this in situ, real-time detection system provides a powerful tool for studying crystallization processes. And the useful dataset were deposited here

Continuous particle manipulation and separation in a hurdle-combined curved microchannel using DC dielectrophoresis

This paper presents a novel dielectrophoresis (DEP)-based microfluidic device which combines round hurdle with an S-shaped curved microchannel for continuous manipulation and separation of microparticles. Local nonuniform electric fields are generated by means of both constricted gaps and curved sections having equal width. Under the effect of negative DEP, particles transporting throughout the microchannel electrokinetically will be directed away from either inner wall or hurdle edge. Both experiment and numerical simulation were conducted, the results of which showed that the trajectories of fix-sized (i.e. 10 or 15 μm) polystyrene (PS) particles could be controlled by adjusting applied voltage, and continuous size-based separation of 10 and 15 μm particles was achieved. Compared to other microchannel designs that make use of either obstacle or curvature individually for electric field gradient, the developed microchannel offers advantages such as improved controllability over particle motion, lower requirement of applied voltage, reduced fouling and particle adhesion, etc. © 2013 AIP Publishing LLC

Intrinsic Piezoelectric Anisotropy of Tetragonal ABO3 Perovskites: A High-Throughput Study

A comprehensive understand of the intrinsic piezoelectric anisotropy stemming from diverse chemical and physical factors is a key step for the rational design of highly anisotropic materials. We performed high-throughput calculations on tetragonal ABO3 perovskites to investigate the piezoelectricity and the interplay between lattice, displacement, polarization and elasticity. Among the 123 types of perovskites, the structural tetragonality is naturally divided into two categories: normal tetragonal (c/a ratio < 1.1) and super-tetragonal (c/a ratio > 1.17), exhibiting distinct ferroelectric, elastic, and piezoelectric properties. Charge analysis revealed the mechanisms underlying polarization saturation and piezoelectricity suppression in the super-tetragonal region, which also produces an inherent contradiction between high d33 and large piezoelectric anisotropy ratio |d33/d31|. The polarization axis and elastic softness direction jointly determine the maximum longitudinal piezoelectric response d33 direction. The validity and deficiencies of the widely utilized |d33/d31| ratio for representing piezoelectric anisotropy were reevaluated

Rapid, one-step preparation of SERS substrate in microfluidic channel for detection of molecules and heavy metal ions

On-chip fabrication of surface-enhanced Raman spectroscopy (SERS)-active materials enables continuous, real-time sensing of targets in the microfluidic chip. However, the current techniques require the time-consuming, complicated process and costly, bulky facilities. In this work, we present a novel method for synthesis of Ag nanostructures in a microfluidic channel via one-step electroless galvanic replacement reaction. The whole reaction could be achieved \u3c10 \u3emins, while the traditional methods take hours. The microfluidic channel has a Cu base, which can reduce Ag ions to Ag nanoparticles in the presence of AgNO3 solution. The new technique enables the label-free sensing of chemical molecules (i.e., methylene blue)and biomolecules (i.e., urea). Two proof-of-concept experiments are performed to verify the utilization of the prepared SERS substrate. First, the microfluidics-assisted SERS sensor is used to detect Hg ions in aqueous solution with high sensitivity and good selectivity. Second, the fabricated SERS-active material can couple with a concentration gradient generator for continuous SERS detection. This simple technique can be used in any laboratory without any bulky equipment and can realize numerous lab-on-a-chip applications with the integration of other microfluidic networks

Special issue on innovative methods and techniques for power and energy systems with high penetration of distributed energy resources [Editorial]

1. Background The contemporary landscape of power and energy systems (P&ESs) is experiencing a significant transformation, marked by the integration of distributed energy resources (DERs) like solar photovoltaics, wind turbines, energy storage systems, and electric vehicles. Although these DERs bring forth myriad benefits, they also introduce challenges in variability management, uncertainty, and cyber vulnerabilities. This special issue of Energy Reports offers a comprehensive perspective on these intertwined challenges and opportunities

Investigation into antiepileptic effect of ganoderic acid A and its mechanism in seizure rats induced by pentylenetetrazole

Ganoderic acid A (GAA) exhibited neuron protection in in vitro epilepsy study, but no study has been done in vivo. Rats were administered (i.p.) pentylenetetrazole daily for 28 days to induce seizure. Rats with grade II or above of epileptic score were divided into three groups and given placebo, sodium valproate, or GAA treatment, respectively, for 7 days. The electrical signals of brain were monitored with electroencephalography (EGG); epileptic behavior was assessed using the Racine scale; morphological changes and apoptosis rate of cortical neurons were assessed with H&E staining and TUNEL staining, respectively. Protein expression of calcium-sensing receptor, p-ERK, p-JNK, and p-p38 in hippocampal tissue and Bcl-2, cleaved caspase-3, and Bax in cortical tissues was observed by Western blot and immunohistochemistry assay, respectively. After GAA treatment, apparent seizure-like EEG with significant arrhythmic disorder and spike waves was reduced or disappeared, and wave amplitude of EEG was reduced significantly. GAA showed similar effect with sodium valproate treatments on epilepsy. There were an apparent improvement of the epileptic behavior and a significant increase in the epileptic latency and shortening of the epileptic duration in the treatment group compared to control. GAA treatment ameliorated the nuclear pyknosis of neurons which appeared seriously in the epilepsy group. GAA treatment significantly reduced the cortical neuron apoptosis of epilepsy and the expression of calcium-sensing receptor, p-P38, p-JNK, cleaved caspase-3, and Bax but increased the expression of both p-ERK and Bcl-2. In conclusion, GAA treatment showed strong antiepileptic effect by decreasing apoptosis in cortical neuron and the expression of calcium-sensing receptor and stimulating the MAPK pathwa

Evidences for pressure-induced two-phase superconductivity and mixed structures of NiTe₂ and NiTe in type-II Dirac semimetal NiTe_(2-x) (x = 0.38 ± 0.09) single crystals

Bulk NiTe₂ is a type-II Dirac semimetal with non-trivial Berry phases associated with the Dirac fermions. Theory suggests that monolayer NiTe₂ is a two-gap superconductor, whereas experimental investigation of bulk NiTe_(1.98) for pressures (P) up to 71.2 GPa do not reveal any superconductivity. Here we report experimental evidences for pressure-induced two-phase superconductivity as well as mixed structures of NiTe₂ and NiTe in Te-deficient NiTe_(2-x) (x = 0.38±0.09) single crystals. Hole-dominant multi-band superconductivity with the P3M1 hexagonal-symmetry structure of NiTe₂ appears at P ≥ 0.5 GPa, whereas electron-dominant single-band superconductivity with the P2/m monoclinic-symmetry structure of NiTe emerges at 14.5 GPa < P < 18.4 GPa. The coexistence of hexagonal and monoclinic structures and two-phase superconductivity is accompanied by a zero Hall coefficient up to ∼ 40 GPa, and the second superconducting phase prevails above 40 GPa, reaching a maximum T_c = 7.8 K and persisting up to 52.8 GPa. Our findings suggest the critical role of Te-vacancies in the occurrence of superconductivity and potentially nontrivial topological properties in NiTe_(2-x)