Eliminating Non-linear Raman Shift Displacement Between Spectrometers via Moving Window Fast Fourier Transform Cross-Correlation

Obtaining consistent spectra by using different spectrometers is of critical importance to the fields that rely heavily on Raman spectroscopy. The quality of both qualitative and quantitative analysis depends on the stability of specific Raman peak shifts across instruments. Non-linear drifts in the Raman shifts can, however, introduce additional complexity in model building, potentially even rendering a model impractical. Fortunately, various types of shift correction methods can be applied in data preprocessing in order to address this problem. In this work, a moving window fast Fourier transform cross-correlation is developed to correct non-linear shifts for synchronization of spectra obtained from different Raman instruments. The performance of this method is demonstrated by using a series of Raman spectra of pharmaceuticals as well as comparing with data obtained by using an existing standard Raman shift scattering procedure. The results show that after the removal of shift displacements, the spectral consistency improves significantly, i.e., the spectral correlation coefficient of the two Raman instruments increased from 0.87 to 0.95. The developed standardization method has, to a certain extent, reduced instrumental systematic errors caused by measurement, while enhancing spectral compatibility and consistency through a simple and flexible moving window procedure

Direct observation of spin polarization in epitaxial Fe3O4(001)/MgO thin films grown by magnetron sputtering

We obtained epitaxial single-crystal Fe3O4(001)/MgO(001) thin films by magnetron sputtering. The high quality of the grown Fe3O4 films was confirmed by reflection high-energy electron diffraction and x-ray photoelectron spectroscopy. Atomic magnetic properties of Fe3O4(001)/MgO(001) were investigated using vibrating sample magnetometry and x-ray magnetic circular dichroism. The values of saturation magnetization and magnetic moment are 407 ± 5 emu/cm3 (3.26 ± 0.04 μ B / (f. u.)) and 3.31 ± 0.15 μ B / (f. u.), respectively, in the Fe3O4 film as thin as 5 nm, which are close to the bulk values. The spin polarization was directly measured using spin-resolved photoemission spectroscopy. The measured spin polarization has a maximum value of -42% ± 3%, which is comparable to the theoretical value for the (2 × 2)R45° reconstructed Fe3O4(001) surface. Furthermore, the film thickness-dependent measurements indicate that the anti-phase boundaries significantly decrease the spin polarization rather than the lattice mismatch. Our results demonstrate that epitaxial Fe3O4(001)/MgO thin films grown by magnetron sputtering have desired magnetic properties, facilitating the potential application of Fe3O4-based spintronic devices

Neutrino Physics with JUNO

The Jiangmen Underground Neutrino Observatory (JUNO), a 20 kton multi-purposeunderground liquid scintillator detector, was proposed with the determinationof the neutrino mass hierarchy as a primary physics goal. It is also capable ofobserving neutrinos from terrestrial and extra-terrestrial sources, includingsupernova burst neutrinos, diffuse supernova neutrino background, geoneutrinos,atmospheric neutrinos, solar neutrinos, as well as exotic searches such asnucleon decays, dark matter, sterile neutrinos, etc. We present the physicsmotivations and the anticipated performance of the JUNO detector for variousproposed measurements. By detecting reactor antineutrinos from two power plantsat 53-km distance, JUNO will determine the neutrino mass hierarchy at a 3-4sigma significance with six years of running. The measurement of antineutrinospectrum will also lead to the precise determination of three out of the sixoscillation parameters to an accuracy of better than 1\%. Neutrino burst from atypical core-collapse supernova at 10 kpc would lead to ~5000inverse-beta-decay events and ~2000 all-flavor neutrino-proton elasticscattering events in JUNO. Detection of DSNB would provide valuable informationon the cosmic star-formation rate and the average core-collapsed neutrinoenergy spectrum. Geo-neutrinos can be detected in JUNO with a rate of ~400events per year, significantly improving the statistics of existing geoneutrinosamples. The JUNO detector is sensitive to several exotic searches, e.g. protondecay via the $p\to K^++\bar\nu$ decay channel. The JUNO detector will providea unique facility to address many outstanding crucial questions in particle andastrophysics. It holds the great potential for further advancing our quest tounderstanding the fundamental properties of neutrinos, one of the buildingblocks of our Universe

Phenolic compounds removal by wet air oxidation based processes

Wet air oxidation (WAO) and catalytic wet air oxidation (CWAO) are efficient processes to degrade organic pollutants in water. In this paper, we especially reviewed the WAO and CWAO processes for phenolic compounds degradation. It provides a comprehensive introduction to the CWAO processes that could be beneficial to the scientists entering this field of research. The influence of different reaction parameters, such as temperature, oxygen pressure, pH, stirring speed are analyzed in detail; Homogenous catalysts and heterogeneous catalysts including carbon materials, transitional metal oxides and noble metals are extensively discussed, among which Cu based catalysts and Ru catalysts were shown to be the most active. Three different kinds of the reactor implemented for the CWAO (autoclave, packed bed and membrane reactors) are illustrated and compared. To enhance the degradation efficiency and reduce the cost of the CWAO process, biological degradation can be combined to develop an integrated technology. (C) Higher Education Press and Springer-Verlag Berlin Heidelberg 2017</p

Phenolic compounds removal by wet air oxidation based processes

Wet air oxidation (WAO) and catalytic wet air oxidation (CWAO) are efficient processes to degrade organic pollutants in water. In this paper, we especially reviewed the WAO and CWAO processes for phenolic compounds degradation. It provides a comprehensive introduction to the CWAO processes that could be beneficial to the scientists entering this field of research. The influence of different reaction parameters, such as temperature, oxygen pressure, pH, stirring speed are analyzed in detail; Homogenous catalysts and heterogeneous catalysts including carbon materials, transitional metal oxides and noble metals are extensively discussed, among which Cu based catalysts and Ru catalysts were shown to be the most active. Three different kinds of the reactor implemented for the CWAO(autoclave, packed bed and membrane reactors) are illustrated and compared. To enhance the degradation efficiency and reduce the cost of the CWAO process, biological degradation can be combined to develop an integrated technology

J. Environ. Sci.

Photocatalytic ozonation of phenol and oxalic acid (OA) was conducted with a Ag+/TiO2 catalyst and different pathways were found for the degradation of different compounds. Ag+ greatly promoted the photocatalytic degradation of contaminants due to its role as an electron scavenger It also accelerated the removal rate of OA in ozonation and the simultaneous process for its complex reaction with oxalate. Phenol could be degraded both in direct ozonation and photolysis, but the TOC removal rates were much higher in the simultaneous processes due to the oxidation of hydroxyl radicals resulting from synergetic effects. The sequence of photo-illumination and ozone exposure in the combined process showed quite different effects in phenol degradation and TOC removal. The synergetic effects in different combined processes were found to be highly related to the properties of the target pollutants. The color change of the solution and TEM result confirmed that Ag+ was easily reduced and deposited on the surface of TiO2 under photo-illumination, and dissolved again into solution in the presence of ozone. This simple cycle of enrichment and distribution of Ag+ can greatly benefit the design of advanced oxidation processes, in which the sequences of ozone and photo-illumination can be varied according to the needs for catalyst recycling and the different properties of pollutants.Photocatalytic ozonation of phenol and oxalic acid (OA) was conducted with a Ag+/TiO2 catalyst and different pathways were found for the degradation of different compounds. Ag+ greatly promoted the photocatalytic degradation of contaminants due to its role as an electron scavenger It also accelerated the removal rate of OA in ozonation and the simultaneous process for its complex reaction with oxalate. Phenol could be degraded both in direct ozonation and photolysis, but the TOC removal rates were much higher in the simultaneous processes due to the oxidation of hydroxyl radicals resulting from synergetic effects. The sequence of photo-illumination and ozone exposure in the combined process showed quite different effects in phenol degradation and TOC removal. The synergetic effects in different combined processes were found to be highly related to the properties of the target pollutants. The color change of the solution and TEM result confirmed that Ag+ was easily reduced and deposited on the surface of TiO2 under photo-illumination, and dissolved again into solution in the presence of ozone. This simple cycle of enrichment and distribution of Ag+ can greatly benefit the design of advanced oxidation processes, in which the sequences of ozone and photo-illumination can be varied according to the needs for catalyst recycling and the different properties of pollutants

Reaction mechanism and metal ion transformation in photocatalytic ozonation of phenol and oxalic acid with Ag~+/TiO_2

Photocatalytic ozonation of phenol and oxalic acid (OA) was conducted with a Ag+/TiO2 catalyst and different pathways were found for the degradation of different compounds. Ag+ greatly promoted the photocatalytic degradation of contaminants due to its role as an electron scavenger It also accelerated the removal rate of OA in ozonation and the simultaneous process for its complex reaction with oxalate. Phenol could be degraded both in direct ozonation and photolysis, but the TOC removal rates were much higher in the simultaneous processes due to the oxidation of hydroxyl radicals resulting from synergetic effects. The sequence of photo-illumination and ozone exposure in the combined process showed quite different effects in phenol degradation and TOC removal. The synergetic effects in different combined processes were found to be highly related to the properties of the target pollutants. The color change of the solution and TEM result confirmed that Ag+ was easily reduced and deposited on the surface of TiO2 under photo-illumination, and dissolved again into solution in the presence of ozone. This simple cycle of enrichment and distribution of Ag+ can greatly benefit the design of advanced oxidation processes, in which the sequences of ozone and photo-illumination can be varied according to the needs for catalyst recycling and the different properties of pollutants