Development of sulfur based polymers for rechargeable lithium batteries

Lithium-ion (Li-ion) batteries are in the front edge of recent achievements concerning energy storage. However, Li-ion devices are reaching their maximum regarding energy density storage which restricts their appiicatíon in systems with large power needs, such as electric vehicles. Driven by this shortcoming, in the last few years, Lithium-Sulfur (Li-S) batteries are being considered as an alternative for the exploitatíon of energy storage and conversion systems with improved performance. Indeed, to the S cathodes is associated a theoretical specifíc capacity of 1672 mA h g-1 and a specifíc energy of 2600 W h kg-\ which are several times higher than the correspondent to other possible systems. The relative low atomic weight of S in comparison with other elements (e.g. cobalt) and the multí-electron transfer reactíons in the pair Li/S are at the source ofthis superior theoretícal performance of Li-S batteries.Este trabalho foi financiado por: projeto POCI-01-0145-FEDER-006984 - Laboratório Associado LSRE-LCM - financiado pelo Fundo Europeu de Desenvolvimento Regional (FEDER), através do COMPETE2020 – Programa Operacional Competitividade e Internacionalização (POCI)info:eu-repo/semantics/publishedVersio

W Boson Inclusive Decays to Quarkonium at the LHC

In this paper, the production rates of quarkonia eta_c, J/psi, eta_b, Upsilon, B_c and B_c^* through W boson decay at the LHC are calculated, at the leading order in both the QCD coupling constant and in v, the typical velocity of the heavy quark inside of mesons. It shows that a sizable number of quarkonia from W boson decay will be produced at the LHC. Comparison with the predictions by using quark fragmentation mechanism is also discussed. Results show that, for the charmonium production through W decay, the difference between predictions by the fragmentation mechanism and complete leading order calculation is around 3%, and it is insensitive to the uncertainties of theoretical parameters; however, for the bottomonium and B_c^(*) productions, the difference cannot be ignored as the fragmentation mechanism is less applicable here due to the relatively large ratio mb/mw.Comment: Updated to match the published version in EPJ

Electrochemical behavior of Ti/Al2O3 interfaces produced by diffusion bonding

In the field of biomedical applications a special interest exists regarding the study of the physicochemical and mechanical behaviour of materials, with special focus on the electrochemical degradation of metal/ceramic interfaces. In fact, etal/ceramic interfaces may be present in several biomedical devices, ranging from external or implantable sensors, to dental implants. Diffusion bonding represents an important technique since, in opposition to other production technologies, such as active metal brazing, avoid the possible liberation of certain chemical components harmful to health. The aim of this work is to study the electrochemical degradation of the interface formed between commercially pure Ti and Al2O3 produced by diffusion bonding, in contact with a physiological solution. The present approach included the evaluation of the contribution of individual and pairs of interfacial layers on the global degradation processes. For this propose d.c. electrochemical techniques were used to monitor the open-circuit potential, and to perform potentiodynamic polarization and galvanic corrosion evaluation. Also, electrochemical impedance spectroscopy was used as a complementary technique of the corrosion behaviour of the interface. Chemical composition and morphology of samples and corrosion products were evaluated by SEM and EDS analysis. According to experimental results, two principal reaction layers were formed in the interface: TiAl and Ti3Al. The TiAl layer appears to be the responsible for the strong increase in corrosion rate of the interface.Fundação para a Ciência e Tecnologia -POCTI/CTM/33384/2000; SFRH/BPD/ 5518/2001

Conformal Affine Toda Soliton and Moduli of IIB Superstring on AdS5×S5AdS_5\times S^5

In this paper we interpret the hidden symmetry of the moduli space of IIB superstring on $AdS_{5}\times S^{5}$ in terms of the chiral embedding in $AdS_{5}$, which turns to be the $\mathbb{CP}^{3}$ conformal affine Toda model. We review how the position $\mu$ of poles in the Riemann-Hilbert formulation of dressing transformation and how the value of loop parameters $\mu$ in the vertex operator of affine algebra determines the moduli space of the soliton solutions, which describes the moduli space of the Green-Schwarz superstring. We show also how this affine SU(4) symmetry affinize the conformal symmetry in the twistor space, and how a soliton string corresponds to a Robinson congruence with twist and dilation spin coefficients $\mu$ of twistor.Comment: Final version, Misprints corrected, Note adde

Measurement of charm production at central rapidity in proton-proton collisions at s=2.76\sqrt{s} = 2.76 TeV

The $p_{\rm T}$-differential production cross sections of the prompt (B feed-down subtracted) charmed mesons D$^0$, D$^+$, and D$^{*+}$ in the rapidity range $|y|<0.5$, and for transverse momentum $1< p_{\rm T} <12$ GeV/$c$, were measured in proton-proton collisions at $\sqrt{s} = 2.76$ TeV with the ALICE detector at the Large Hadron Collider. The analysis exploited the hadronic decays D$^0 \rightarrow$K$\pi$, D$^+ \rightarrow$K$\pi\pi$, D$^{*+} \rightarrow$D$^0\pi$, and their charge conjugates, and was performed on a $L_{\rm int} = 1.1$ nb$^{-1}$ event sample collected in 2011 with a minimum-bias trigger. The total charm production cross section at $\sqrt{s} = 2.76$ TeV and at 7 TeV was evaluated by extrapolating to the full phase space the $p_{\rm T}$-differential production cross sections at $\sqrt{s} = 2.76$ TeV and our previous measurements at $\sqrt{s} = 7$ TeV. The results were compared to existing measurements and to perturbative-QCD calculations. The fraction of cdbar D mesons produced in a vector state was also determined.Comment: 20 pages, 5 captioned figures, 4 tables, authors from page 15, published version, figures at http://aliceinfo.cern.ch/ArtSubmission/node/307

Particle-yield modification in jet-like azimuthal di-hadron correlations in Pb-Pb collisions at sNN\sqrt{s_{\rm NN}} = 2.76 TeV

The yield of charged particles associated with high-$p_{\rm T}$ trigger particles ($8 < p_{\rm T} < 15$ GeV/$c$) is measured with the ALICE detector in Pb-Pb collisions at $\sqrt{s_{\rm NN}}$ = 2.76 TeV relative to proton-proton collisions at the same energy. The conditional per-trigger yields are extracted from the narrow jet-like correlation peaks in azimuthal di-hadron correlations. In the 5% most central collisions, we observe that the yield of associated charged particles with transverse momenta $p_{\rm T}> 3$ GeV/$c$ on the away-side drops to about 60% of that observed in pp collisions, while on the near-side a moderate enhancement of 20-30% is found.Comment: 15 pages, 2 captioned figures, 1 table, authors from page 10, published version, figures at http://aliceinfo.cern.ch/ArtSubmission/node/350

SpectraNet–53: A deep residual learning architecture for predicting soluble solids content with VIS–NIR spectroscopy

This work presents a new deep learning architecture, SpectraNet-53, for quantitative analysis of fruit spectra, optimized for predicting Soluble Solids Content (SSC, in Brix). The novelty of this approach resides in being an architecture trainable on a very small dataset, while keeping a performance level on-par or above Partial Least Squares (PLS), a time-proven machine learning method in the field of spectroscopy. SpectraNet-53 performance is assessed by determining the SSC of 616 Citrus sinensi L. Osbeck 'Newhall' oranges, from two Algarve (Portugal) orchards, spanning two consecutive years, and under different edaphoclimatic conditions. This dataset consists of short-wave near-infrared spectroscopic (SW-NIRS) data, and was acquired with a portable spectrometer, in the visible to near infrared region, on-tree and without temperature equalization. SpectraNet-53 results are compared to a similar state-of-the-art architecture, DeepSpectra, as well as PLS, and thoroughly assessed on 15 internal validation sets (where the training and test data were sampled from the same orchard or year) and on 28 external validation sets (training/test data sampled from different orchards/years). SpectraNet-53 was able to achieve better performance than DeepSpectra and PLS in several metrics, and is especially robust to training overfit. For external validation results, on average, SpectraNet-53 was 3.1% better than PLS on RMSEP (1.16 vs. 1.20 Brix), 11.6% better in SDR (1.22 vs. 1.10), and 28.0% better in R2 (0.40 vs. 0.31).project NIBAP ALG-01-0247-FEDER-037303, project OtiCalFrut ALG-010247-FEDER-033652info:eu-repo/semantics/publishedVersio

Impact of dietary Chlorella vulgaris and carbohydrate-active enzymes incorporation on plasma metabolites and liver lipid composition of broilers

Research Areas: Veterinary SciencesBackground: Chlorella vulgaris has been proposed as a sustainable green feedstock in poultry nutrition due to its ease of cultivation, minimal environmental impact and balanced nutritional composition. However, the majority of studies documents the use of C. vulgaris as a dietary supplement in broilers instead of a feed ingredient. To the best of our knowledge, no report has shown the effect of a high-level incorporation (>2 % in the diet) of C. vulgaris on plasma metabolites and hepatic lipid composition of broilers. One hundred and twenty Ross 308 male birds were housed in 40 wired-floor cages and randomly distributed by the following experimental diets at 22 days of age (n = 10) during 15 days: (1) a corn-soybean meal based diet (control); (2) based diet with 10% of C. vulgaris; (3) diet 2 supplemented with 0.005% Rovabio® Excel AP; and (4) diet 2 supplemented with 0.01% of a pre-selected four-CAZyme mixture. Results: The inclusion of C. vulgaris at 10% in the diet, regardless of the presence of exogenous CAZymes, changed plasma metabolites but did not compromise broilers growth. Plasma total lipids increased in broilers fed C. vulgaris combined with the two feed CAZymes (p < 0.001) compared with the control diet. Moreover, the supplementation with Rovabio® increased total cholesterol and LDL-cholesterol, while the addition of the four-CAZyme mixture increased triacylglycerols, VLDL-cholesterol and ALP activity. In opposition, HDL-cholesterol levels decreased in broilers fed microalga alone (p = 0.002). Regarding hepatic composition, the inclusion of C. vulgaris in broiler diets, individually or combined with exogenous CAZymes, had a minor effect on fatty acids but improved the n-6/n-3 ratio and total carotenoids. Conclusions: In summary, the inclusion of a high level (10%) of C. vulgaris in broiler´s diet, regardless of the presence of exogenous CAZymes, improved hepatic antioxidant composition and did not impair broiler’s performance. In addition, the feed supplementation with CAZymes increased broilers lipemia. Therefore, dietary C. vulgaris at this incorporation level seems to be safe for animal health and do not compromise performance traits, with no need of CAZymes supplementation.info:eu-repo/semantics/publishedVersio

Biodegradation of mono-, di- and trifluoroacetate by microbial cultures with different origins

This work focused on the biodegradation of three structurally related fluoroacetates (FAs), mono- (MFA), di- (DFA) and trifluoroacetate (TFA), using as microbial inocula samples collected from a site with a long history of industrial contamination and activated sludge obtained from a municipal wastewater treatment plant. Biodegradation experiments were carried out under different modes of substrate supplementation, which included (i) FAs fed as sole carbon sources; (ii) FAs (only for DFA and TFA) fed in co-metabolism with sodium acetate; and (iii) mixtures of MFA with DFA or TFA. Biodegradation of the target compounds was assessed through fluoride ion release. Defluorination was obtained in the cultures fed with MFA, while DFA and TFA were recalcitrant in all tested conditions. When present in mixture, DFA was shown to inhibit biodegradation of MFA, while TFA had no effect. A total of 13 bacterial isolates obtained from MFA degrading cultures were found to degrade 20mgL-1 of this compound, as single strains, when supplemented as a sole carbon source. Sequencing of the 16S rRNA gene indicated that among these degrading bacteria only Delftia acidovorans had been previously reported to be able to degrade MFA. This work shows that, despite their similar chemical structures, biodegradation of the three tested FAs is very distinct and draws attention to the unknown impacts that the accumulation of DFA and TFA may have in the environment as a result of their high recalcitrance.info:eu-repo/semantics/publishedVersio

Intensification of heterogeneous photocatalysis by applying a kenics® static mixer as catalyst support

Despite scientific community’s efforts, overcoming mass and photon transfer limitations remain a main challenge for heterogeneous photocatalysis with immobilized catalysts. Here, a Kenics® static mixer was used for the first time as catalyst support for heterogeneous photocatalysis in tubular reactors. This permitted not only to take advantage of the enhanced mass transfer supplied by the intense mixing, but also to provide a total illumination of the photocatalyst surface area with front-irradiation mechanism by using sunlight combined with compound parabolic collectors. Stainless steel Kenics® static mixers were coated with TiO2 or Fe2O3 photocatalyst and applied for oxytetracycline (OTC) degradation in aqueous solutions. The photocatalytic efficiency was evaluated as a function of different parameters: (i) catalyst deposition technique (dip coating or spray coating), (ii) photocatalyst film thickness, (iii) oxidant (H2O2) concentration, and (iv) number of static mixing elements.info:eu-repo/semantics/publishedVersio