Setting the photoelectron clock through molecular alignment

The interaction of strong laser fields with matter intrinsically provides a powerful tool for imaging transient dynamics with an extremely high spatiotemporal resolution. Here, we study strong-field ionisation of laser-aligned molecules, and show a full real-time picture of the photoelectron dynamics in the combined action of the laser field and the molecular interaction. We demonstrate that the molecule has a dramatic impact on the overall strong-field dynamics: it sets the clock for the emission of electrons with a given rescattering kinetic energy. This result represents a benchmark for the seminal statements of molecular-frame strong-field physics and has strong impact on the interpretation of self-diffraction experiments. Furthermore, the resulting encoding of the time-energy relation in molecular-frame photoelectron momentum distributions shows the way of probing the molecular potential in real-time, and accessing a deeper understanding of electron transport during strong-field interactions

Biobased chemicals from the catalytic depolymerization of Kraft lignin using supported noble metal-based catalysts

Kraft lignin, a side-product of the paper industry, is considered an attractive feedstock for the production of biorenewable chemicals. However, its recalcitrant nature and sulfur content render catalytic conversions challenging. This study demonstrates the efficacy of noble metal-based catalysts for the production of a lignin oil enriched in alkylphenolic and aromatic compounds, by a catalytic hydrotreatment of Kraft lignin without the use of an external solvent. Eight commercially available catalysts were evaluated using four different metals (Ru, Pt, Pd, Rh) on two supports (activated carbon and Al2O3). The product oils were extensively analyzed by means of GPC, GCxGC-FID, GC-MS-FID, and elemental analysis. The catalysts were characterized by various techniques (N-2 physisorption, NH3-TPD, XRD and TEM) before and after reaction, and their physico-chemical properties were correlated with catalytic performance. Al2O3 as support gave better results than carbon as support in terms of lignin oil yield and composition, due to a combination of higher total acidity, mildly acidic sites and a mesoporous structure. The metallic phase also significantly affected product distribution. The best results were obtained using a Rh/Al2O3 catalyst, resulting in a lignin oil yield of 36.3 wt% on a lignin intake and a total monomer yield of 30.0 wt% on lignin intake including 15.3 wt% of alkylphenolic and 7.9 wt% of aromatic compounds, and with a sulfur content <0.01 wt%

Fatal cytokine release syndrome by an aberrant FLIP/STAT3 axis

Inflammatory responses rapidly detect pathogen invasion and mount a regulated reaction. However, dysregulated anti-pathogen immune responses can provoke life-threatening inflammatory pathologies collectively known as cytokine release syndrome (CRS), exemplified by key clinical phenotypes unearthed during the SARS-CoV-2 pandemic. The underlying pathophysiology of CRS remains elusive. We found that FLIP, a protein that controls caspase-8 death pathways, was highly expressed in myeloid cells of COVID-19 lungs. FLIP controlled CRS by fueling a STAT3-dependent inflammatory program. Indeed, constitutive expression of a viral FLIP homolog in myeloid cells triggered a STAT3-linked, progressive, and fatal inflammatory syndrome in mice, characterized by elevated cytokine output, lymphopenia, lung injury, and multiple organ dysfunctions that mimicked human CRS. As STAT3-targeting approaches relieved inflammation, immune disorders, and organ failures in these mice, targeted intervention towards this pathway could suppress the lethal CRS inflammatory state

Wacker-oxidation of Ethylene over Pillared Layered Material Catalysts

This paper concerns the Wacker oxidation of ethylene by oxygen in the presence of water over supported Pd/VOx catalysts. High surface area porous supports were obtained from layer-structured materials, such as, montmorillonite (MT), laponite (LT) (smectites), and hydrotalcite (layered double hydroxide, LDH) by pillaring. Before introduction of Pd, supports MT and LDH were pillared by vanadia. The laponite was used in titania-pillared form (TiO2-LAP) as support of Pd/VOx active component. Acetaldehyde (AcH), acetic acid (AcOH) and CO2 were the products with yields and selectivities, depending on the reaction conditions and the properties of the applied catalyst. Under comparable conditions the pillared smectite catalysts gave higher AcH yield than the pillared LDH catalyst. UV vis spectroscopic examination suggested that the pillared smectites contained polymeric chains of VO4, whereas only isolated monomeric VO4 species were present in the pillared LDH. The higher catalytic activity in the Wacker oxidation was attributed to the more favorable redox property of the polymeric than of the monomeric vanadia. The V3+ ions in the polymeric species can reduce O2 to O2- ions, whereas the obtained V5+ ions are ready to pass over O to Pd0 to generate PdO whereon the oxidation of the ethylene proceeds

EMERGENCY PLANNING IN CASE OF CBRN EVENTS: AN INNOVATIVE METHODOLOGY TO IMPROVE THE SAFETY KNOWLEDGE OF ADVISORS AND FIRST RESPONDERS BY A MULTIDISCIPLINARY TABLE TOP EXERCISE.

ABSTRACT Nowadays Chemical-Biological-Radiological-Nuclear (CRBN) risks are one of the main safety concern. The radiological disasters of Fukushima and Chernobyl, the chemical events of Seveso or the release of Sarin in the Tokio Subway,and the biological emergencies such as the H1N1 flue represent few examples of a dreadful evidence: : CBRNe risks are a real and global threat around us. A CBRNe event can be either of an intentional and un-intentional nature and it is important to have highly specialized advisors that can support decision makers and first responders to face this threat. The University of Rome Tor Vergata, in collaboration with the most important Italian and International Bodies that work in the field of CBRN safety and security and supported by NATO and OPCW, organized two International Master Courses in Protection against CBRN events. In this context, a Table Top Exercise (TTX) was organized, in collaboration with the Ministry of Interior and Ministry of Defence, taking into account that, in each country, the system response to CBRNe events strongly depends also on law and procedures, that enforce the advisors and first responders to rely with different skills and roles in function of the administration of origin. The organized TTX was aimed to test the level preparation of the Master students and experts working in Italy in the field of CBRN events and to test the emergency planning preparation. In particular, a radiological release was simulated in a Harbour facility in Urban Area. The students were divided in multidisciplinary groups with heterogeneous competences. Each group was supported by CBRNì experts and was stressed by the injects from a Command and Operative Centre. Responsiveness to the injects and to the stress together with the ability to organize and manage safety and security operations, but also to interpret each role in the team according to according to national laws, were evaluated for each group. The scenario, the logistic organization, on-going adjustments during the exercise and the outcomes will be presented and analyzed by the authors in this paper. PRELIMINARY INDEX 1. Abstract 2. Introduction 3. Table Top Exercise (TTX) 3.1 What is a TTX 3.2 How the TTX is organized 3.3 Scenario and injects 3.4 Organizational and technical solutions 4. Dat

DFT and kinetic evidences of the preferential CO oxidation pattern of manganese dioxide catalysts in hydrogen stream (PROX)

The oxidation functionality of Mn(IV) sites has been assessed by density functional theory (DFT) analysis of adsorption and activation energies of CO, H2 and O2 on a model Mn4O8 cluster. DFT calculations indicate that Mn(IV) atoms prompt an easy CO conversion to CO2 via a reaction path involving both catalyst and gas-phase oxygen species, while much greater energy barriers hinder H2 oxidation. Accordingly, a MnCeOx catalyst (Mnat/Ceat, 5) with large exposure of Mn(IV) sites shows a remarkable CO oxidation performance at T ≥ 293 K and no H2 oxidation activity below 393 K. Empiric kinetics disclose that the catalyst-oxygen abstraction step determines both CO and H2 oxidation rate, although different activation energies favor the preferential oxidation (PROX) pattern of the studied catalyst (353–423 K). Conversion-selectivity of 100%, high stability during 72 h reaction time and moderate inhibiting effects of water and CO2 feeding reveal the potential of MnO2 materials as efficient, low-cost and robust PROX catalysts

How surface and textural properties affect the behaviour of Mn-based catalysts during transesterification reaction to produce biodiesel

This work was aimed at investigating the catalytic behaviour of MnCeOx and MnZrOx systems in biodiesel production by sunflower oil transesterification reaction with methanol. Surface and textural properties were deeply investigated by different techniques whereas CH3OH surface reactivity was evaluated by FT-IR and MeOH-TPSR measurements, in order to disclose the nature of the active sites and to provide evidences of a complex reaction mechanism, in which a synergic role of Mn and carrier significantly affects the methyl esters productivity. Direct relationship among catalytic activity, density of strong basic sites and amount of adsorbed bidentate methoxy species were found. The doubly-bridging coordinated methoxy species were recognized as the ones mainly involved in the transesterification reaction. Anyway, even if the basic strength resulted to be considered the key factor for MeOH activation, only the proper balance between basic and acid sites controls catalyst behaviour. The linear dependence of activity with catalyst porosity clearly demonstrated that a wide porous structure is required to enhance the sites accessibility to large triglycerides (TGs) molecules