Pulsed Streamer Discharge Characteristics of Ozone Production in Dry Air

Experimental investigation of HV short pulsed streamer discharges in dry air-fed ozonizers under various operating conditions are reported. Ozone concentration, energy input and ozone production yield (efficiency) were measured at various voltages (14 to 37 kV), pulse repetition rates (25 to 400 pulses per second, pps), flow rates (1.5 to 3.0 1/min) and different gap spacings (10 to 20 mm) at a pressure of 1.01×105 Pa in dry air. A spiral copper wire (1 mm in diameter) made to a cylindrical configuration (18 to 38 mm in diameter) in a concentric coaxial electrode system of various dimensions was employed. A magnetic pulse compressor provided the HV and current pulses. Higher voltage and higher repetition rates yielded higher concentrations of ozone at a fixed air flow rate. The present investigation was extended to assess the performance of this pulsed ozone generator using dry air under desired conditions of high concentration and high yield of ozone for industrial applications

Pulsed Power Production of Ozone in 02/N2 iin a Coaxial Reactor without Dielectric Layer

Very short duration pulsed streamer discharges have been used to produce ozone in a gas mixture of nitrogen and oxygen at atmospheric pressure. The ratio of nitrogen to oxygen in the mixture was varied in the range from 2.5/0.5 to 0.5/2.5, while maintaining a total flow rate of 3 l/min. The production of ozone was found to be higher for a specific mixture ratio of N2/O2 than that in oxygen or in dry air. The production of ozone in O2 was higher than that in dry air. The production yield of ozone (g/kWh) increased with decreasing nitrogen in the O2/N2 mixture. It has been found that the peak of the streamer discharge current decreased with time after application of the pulsed power. This decrease in the current corresponded with the increase in the ozone production and is attributed to the loss of electrons in the discharge current due to their attachment to ozone to form negative ions

Ozone Production Using Pulsed Dielectric Barrier Discharge in Oxygen

The production of ozone was investigated using a dielectric barrier discharge in oxygen, and employing short-duration pulsed power. The dependence of the ozone concentration (parts per million, ppm) and ozone production yield (g(O3)/kWh) on the peak pulsed voltage (17.5 to 57.9 kV) and the pulse repetition rate (25 to 400 pulses/s, pps) were investigated. In the present study, the following parameters were kept constant: a pressure of 1.01×105 Pa, a temperature of 26±4°C a gas flow rate of 3.0 1/min and a gaseous gap length of 11 mm. A concentric coaxial cylindrical reactor was used. A spiral copper wire (1 mm in diameter) was wound on a polyvinylchloride (PVC) cylindrical configuration (26 mm in diameter) and placed centrally in a concentric coaxial electrode system with 4 mm thick PVC dielectric layer adjacent to a copper outer electrode of 58 mm in internal diameter. HV and current pulses were provided by a magnetic pulse compressor power source

Spectroscopy of 32Ne and the Island of Inversion

We report on the first spectroscopic study of the N=22 nucleus 32Ne at the newly completed RIKEN Radioactive Ion Beam Factory. A single gamma-ray line with an energy of 722(9) keV was observed in both inelastic scattering of a 226 MeV/u 32Ne beam on a Carbon target and proton removal from 33Na at 245 MeV/u. This transition is assigned to the de-excitation of the first J^pi = 2+ state in 32Ne to the 0+ ground state. Interpreted through comparison with state-of-the-art shell model calculations, the low excitation energy demonstrates that the Island of Inversion extends to at least N=22 for the Ne isotopes.Comment: Accepted for publication in Phys. Rev. Lett. 11 pages, 3 figure

Ozone Generation in Dry Air Using Pulsed Discharges With and Without a Solid Dielectric Layer

Energy efficient generation of ozone is very important because ozone is being used increasingly in a wide range of industrial applications. Ozonizers usually use dielectric barrier discharges and employ alternating current (ac) with consequent heat generation, which necessitates cooling. In the present study, very short duration pulsed voltage is employed resulting in reduced heating of the gas and discharge reactor. A comparison of ozone generation in dry air using a coaxial concentric electrode system with and without a solid dielectric layer is reported. Two types of dielectric layers were employed, ceramic and polyvinylchloride (PVC). The effects of peak pulsed voltage (12.5 to 62 kV), reactor length (0.1 to 1 m), pulse repetition rate (25 to 400 pulses per second, pps), gas flow rate (1.5 to 3.0 l/min) and variation of the pitch length of the spiral wire forming the central electrode (5 to 10 mm) on the concentration and production yield of ozone (g/kWh) are reported. A comparison is made between the performance of discharge reactors with (ceramic reactor Type IIC and PVC reactor Type IIP) and without (reactor Type I) a dielectric layer, using the same electrode gap separation (15 mm) and reactor lengths (0.157 and 1 m). High production yields of ozone in dry air of ∼ 122, 52 and 60 g/kWh were obtained when using, respectively ceramic, PVC, and no dielectric layer, for a fixed pulse rate of 100 pps, 1.5 l/min flow rate and for a relatively short length of the reactor of 157 mm

Global Mapping of Cell Type–Specific Open Chromatin by FAIRE-seq Reveals the Regulatory Role of the NFI Family in Adipocyte Differentiation

Identification of regulatory elements within the genome is crucial for understanding the mechanisms that govern cell type–specific gene expression. We generated genome-wide maps of open chromatin sites in 3T3-L1 adipocytes (on day 0 and day 8 of differentiation) and NIH-3T3 fibroblasts using formaldehyde-assisted isolation of regulatory elements coupled with high-throughput sequencing (FAIRE-seq). FAIRE peaks at the promoter were associated with active transcription and histone modifications of H3K4me3 and H3K27ac. Non-promoter FAIRE peaks were characterized by H3K4me1+/me3-, the signature of enhancers, and were largely located in distal regions. The non-promoter FAIRE peaks showed dynamic change during differentiation, while the promoter FAIRE peaks were relatively constant. Functionally, the adipocyte- and preadipocyte-specific non-promoter FAIRE peaks were, respectively, associated with genes up-regulated and down-regulated by differentiation. Genes highly up-regulated during differentiation were associated with multiple clustered adipocyte-specific FAIRE peaks. Among the adipocyte-specific FAIRE peaks, 45.3% and 11.7% overlapped binding sites for, respectively, PPARγ and C/EBPα, the master regulators of adipocyte differentiation. Computational motif analyses of the adipocyte-specific FAIRE peaks revealed enrichment of a binding motif for nuclear family I (NFI) transcription factors. Indeed, ChIP assay showed that NFI occupy the adipocyte-specific FAIRE peaks and/or the PPARγ binding sites near PPARγ, C/EBPα, and aP2 genes. Overexpression of NFIA in 3T3-L1 cells resulted in robust induction of these genes and lipid droplet formation without differentiation stimulus. Overexpression of dominant-negative NFIA or siRNA–mediated knockdown of NFIA or NFIB significantly suppressed both induction of genes and lipid accumulation during differentiation, suggesting a physiological function of these factors in the adipogenic program. Together, our study demonstrates the utility of FAIRE-seq in providing a global view of cell type–specific regulatory elements in the genome and in identifying transcriptional regulators of adipocyte differentiation

Fragile X Mental Retardation Protein Regulates Proliferation and Differentiation of Adult Neural Stem/Progenitor Cells

Fragile X syndrome (FXS), the most common form of inherited mental retardation, is caused by the loss of functional fragile X mental retardation protein (FMRP). FMRP is an RNA–binding protein that can regulate the translation of specific mRNAs. Adult neurogenesis, a process considered important for neuroplasticity and memory, is regulated at multiple molecular levels. In this study, we investigated whether Fmrp deficiency affects adult neurogenesis. We show that in a mouse model of fragile X syndrome, adult neurogenesis is indeed altered. The loss of Fmrp increases the proliferation and alters the fate specification of adult neural progenitor/stem cells (aNPCs). We demonstrate that Fmrp regulates the protein expression of several components critical for aNPC function, including CDK4 and GSK3β. Dysregulation of GSK3β led to reduced Wnt signaling pathway activity, which altered the expression of neurogenin1 and the fate specification of aNPCs. These data unveil a novel regulatory role for Fmrp and translational regulation in adult neurogenesis

Differential Deployment of REST and CoREST Promotes Glial Subtype Specification and Oligodendrocyte Lineage Maturation

The repressor element-1 (RE1) silencing transcription factor/neuron-restrictive silencer factor (REST/NRSF) is a master transcriptional regulator that binds to numerous genomic RE1 sites where it acts as a molecular scaffold for dynamic recruitment of modulatory and epigenetic cofactors, including corepressor for element-1-silencing transcription factor (CoREST). CoREST also acts as a hub for various cofactors that play important roles in epigenetic remodeling and transcriptional regulation. While REST can recruit CoREST to its macromolecular complex, CoREST complexes also function at genomic sites independently of REST. REST and CoREST perform a broad array of context-specific functions, which include repression of neuronal differentiation genes in neural stem cells (NSCs) and other non-neuronal cells as well as promotion of neurogenesis. Despite their involvement in multiple aspects of neuronal development, REST and CoREST are not believed to have any direct modulatory roles in glial cell maturation.We challenged this view by performing the first study of REST and CoREST in NSC-mediated glial lineage specification and differentiation. Utilizing ChIP on chip (ChIP-chip) assays, we identified distinct but overlapping developmental stage-specific profiles for REST and CoREST target genes during astrocyte (AS) and oligodendrocyte (OL) lineage specification and OL lineage maturation and myelination, including many genes not previously implicated in glial cell biology or linked to REST and CoREST regulation. Amongst these factors are those implicated in macroglial (AS and OL) cell identity, maturation, and maintenance, such as members of key developmental signaling pathways and combinatorial transcription factor codes.Our results imply that REST and CoREST modulate not only neuronal but also glial lineage elaboration. These factors may therefore mediate critical developmental processes including the coupling of neurogenesis and gliogenesis and neuronal-glial interactions that underlie synaptic and neural network plasticity and homeostasis in health and in specific neurological disease states