8,783 research outputs found
Time-resolved infrared absorption spectroscopy applied to photoinduced reactions: how and why
Abstract: Time-resolved infrared (IR) spectroscopy is a widely used technique in the investigation of photoinduced reactions, given its capabilities of providing structural information about the presence of intermediates and the reaction mechanism. Despite the fact that it is used in several fields since the â80s, the communication between the different scientific communities (photochemists, photobiologists, etc.) has been to date quite limited. In some cases, this lack of communication happenedâand still happensâeven inside the same scientific community (for instance between specialists in ultrafast ps/fs IR and those in âfastâ ns/”s/ms IR). Even more surprising is the difficulty of non-specialists to understand the potential of time-resolved IR spectroscopy, despite the fact that IR spectroscopy is normally taught to all chemistry and material science students, and to several biology and physics students. This tutorial review aims at helping to solve these issues, first by providing a comprehensive but reader-friendly overview of the different techniques, and second, by focusing on five âcase studiesâ (from photobiology, gas-phase photocatalysis, photochemistry, semiconductors and metal-carbonyl complexes). We are confident that this approach can help the readerâwhichever is its backgroundâto understand the capabilities of time-resolved IR spectroscopy to study the mechanism of photoinduced reactions. Graphical Abstract: [Figure not available: see fulltext.
Dual-curable stereolithography resins for superior thermomechanical properties
Stereolithography (SL) stands out as a relatively fast additive manufacturing method to produce thermoset components with high resolutions. The majority of SL resins consist of acrylate monomers which result in materials with cur-ing-induced shrinkage problems and this, in addition to the incomplete and non-uniform conversions reached in the SL process, results in poor mechanical properties. To address this issue, a dual-curing formulation was developed by mixing an epoxy monomer into a commercial multi-acrylate SL resin: the first curing stage is acrylate free-radical photopolymerization at ambient temperature, and the second curing stage is cationic epoxy homopolymerization at higher temperatures. The fully dual-cured materials are macroscopically homogeneous, with nanoscale domains observed by Atomic Force Mi-croscopy (AFM), and with unimodal tan delta peaks observed in Dynamic Mechanical Analysis (DMA). The uncured material was storage stable at ambient conditions for at least 9 weeks since the epoxy part was virtually unreactive at these temper-atures. With the dual-cured materials, a nearly 10-fold increase in Youngâs modulus was achieved over the neat acrylate resin. At the thermal curing stage, the presence of diperoxyketal thermal radical initiator to the liquid formulation facilitated the polymerization of unreacted acrylates that remained from the SL process simultaneously with epoxy homopolymerization and helped the material attain improved properties
Measurement of {\eta} meson production in {\gamma}{\gamma} interactions and {\Gamma}({\eta}-->{\gamma}{\gamma}) with the KLOE detector
We present a measurement of {\eta} meson production in photon-photon
interactions produced by electron-positron beams colliding with \sqrt{s}=1 GeV.
The measurement is done with the KLOE detector at the \phi-factory DA{\Phi}NE
with an integrated luminosity of 0.24 fb^{-1}. The e^+e^- --> e^+e^-{\eta}
cross section is measured without detecting the outgoing electron and positron,
selecting the decays {\eta}-->{\pi}^+{\pi}^-{\pi}^0 and
{\eta}-->{\pi}^0{\pi}^0{\pi}^0. The most relevant background is due to e^+e^-
--> {\eta}{\gamma} when the monochromatic photon escapes detection. The cross
section for this process is measured as {\sigma}(e^+e^- -->{\eta}{\gamma}) =
(856 \pm 8_{stat} \pm 16_{syst}) pb. The combined result for the e^+e^-
-->e^+e^-{\eta} cross section is {\sigma}(e^+e^- -->e^+e^-{\eta}) = (32.72 \pm
1.27_{stat} \pm 0.70_{syst}) pb. From this we derive the partial width
{\Gamma}({\eta}-->{\gamma}{\gamma}) = (520 \pm 20_{stat} \pm 13_{syst}) eV.
This is in agreement with the world average and is the most precise measurement
to date.Comment: Version accepted by JHE
A new limit on the CP violating decay KS -> 3pi0 with the KLOE experiment
We have carried out a new direct search for the CP violating decay KS -> 3pi0
with 1.7 fb^-1 of e+e- collisions collected by the KLOE detector at the
phi-factory DAFNE. We have searched for this decay in a sample of about 5.9 x
10^8 KS KL events tagging the KS by means of the KL interaction in the
calorimeter and requiring six prompt photons. With respect to our previous
search, the analysis has been improved by increasing of a factor four the
tagged sample and by a more effective background rejection of fake KS tags and
spurious clusters. We find no candidates in data and simulated background
samples, while we expect 0.12 standard model events. Normalizing to the number
of KS -> 2pi0 events in the same sample, we set the upper limit on BR(KS ->
3pi0 < 2.6 x 10^-8 at 90% C.L., five times lower than the previous limit. We
also set the upper limit on the eta_000 parameter, |eta_000 | < 0.0088 at 90%
C.L., improving by a factor two the latest direct measurement.Comment: Accepted for publication in Physics Letters B (15 pages, 13 figures
Measurement of the pseudoscalar mixing angle and gluonium content with KLOE detector
We have measured the ratio by looking for the radiative decays and in the final states
7 's and 7 's respectively, in a sample of mesons produced at the Frascati -factory. We
obtain from which we
derive . In the hypothesis of
no gluonium content we extract the pseudoscalar mixing angle in the
quark-flavor basis .
Combining the value of with other constraints, we estimate the
gluonium fractional content of meson as and
the mixing angle .Comment: 13 pages, 8 figure
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias
Background and purpose:â These EFNS guidelines on the molecular diagnosis of neurogenetic disorders are designed to provide practical help for the general neurologist to make appropriate use of molecular genetics in diagnosing neurogenetic disorders.Methods:â Literature searches were performed before expert members of the task force wrote proposals, which were discussed in detail until final consensus had been reached among all task force members.Results and conclusion:â This paper provides updated guidelines for molecular diagnosis of two particularly complex groups of disorders, the ataxias and spastic paraplegias. Possibilities and limitations of molecular genetic diagnosis of these disorders are evaluated and recommendations are provided
Power Doppler signal at the enthesis and bone erosions are the most discriminative OMERACT ultrasound lesions for SpA: Results from the DEUS (Defining Enthesitis on Ultrasound in Spondyloarthritis) multicentre study
Objectives To assess, in spondyloarthritis (SpA), the discriminative value of the Outcome Measures in Rheumatology (OMERACT) ultrasound lesions of enthesitis and their associations with clinical features in this population. Methods In this multicentre study involving 20 rheumatology centres, clinical and ultrasound examinations of the lower limb large entheses were performed in 413 patients with SpA (axial SpA and psoriatic arthritis) and 282 disease controls (osteoarthritis and fibromyalgia). 'Active enthesitis' was defined as (1) power Doppler (PD) at the enthesis grade â„1 plus entheseal thickening and/or hypoechoic areas, or (2) PD grade >1 (independent of the presence of entheseal thickening and/or hypoechoic areas). Results In the univariate analysis, all OMERACT lesions except enthesophytes/calcifications showed a significant association with SpA. PD (OR=8.77, 95% CI 4.40 to 19.20, p<0.001) and bone erosions (OR=4.75, 95% CI 2.43 to 10.10, p<0.001) retained this association in the multivariate analysis. Among the lower limb entheses, only the Achilles tendon was significantly associated with SpA (OR=1.93, 95% CI 1.30 to 2.88, p<0.001) in the multivariate analyses. Active enthesitis showed a significant association with SpA (OR=9.20, 95% CI 4.21 to 23.20, p<0.001), and unlike the individual OMERACT ultrasound lesions it was consistently associated with most clinical measures of SpA disease activity and severity in the regression analyses. Conclusions This large multicentre study assessed the value of different ultrasound findings of enthesitis in SpA, identifying the most discriminative ultrasound lesions and entheseal sites for SpA. Ultrasound could differentiate between SpA-related enthesitis and other forms of entheseal pathology (ie, mechanical enthesitis), thus improving the assessment of entheseal involvement in SpA
A global fit to determine the pseudoscalar mixing angle and the gluonium content of the eta' meson
We update the values of the eta-eta' mixing angle and of the eta' gluonium
content by fitting our measurement R_phi = BR(phi to eta' gamma)/ BR(phi to eta
gamma) together with several vector meson radiative decays to pseudoscalars (V
to P gamma), pseudoscalar mesons radiative decays to vectors (P to V gamma) and
the eta' to gamma gamma, pi^0 to gamma gamma widths. From the fit we extract a
gluonium fraction of Z^2_G = 0.12 +- 0.04, the pseudoscalar mixing angle psi_P
= (40.4 +- 0.6) degree and the phi-omega mixing angle psi_V = (3.32 +- 0.09)
degree. Z^2_G and psi_P are fairly consistent with those previously published.
We also evaluate the impact on the eta' gluonium content determination of
future experimental improvements of the eta' branching ratios and decay width.Comment: 13 pages, 7 figures to submit to JHE
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