276 research outputs found
Primjena mikrokapsula antocijanina, izoliranih iz ploda palme Euterpe edulis Mart., u proizvodnji hrane, te ispitivanje njihove stabilnosti pomoÄu toplinsko-analitiÄkih metoda i fotoakustiÄne spektroskopije
Anthocyanins extracted from the pulp of the fruit of juçara palm (Euterpe edulis Mart.) were microencapsulated with maltodextrin in order to stabilise them. Photoacoustic spectroscopy was used to investigate the photostability of the microencapsulated samples. Complementary differential scanning calorimetry and scanning electron microscopy measurements were also performed. Lyophilised extract had 14 340.2 mg/L of total anthocyanins, and the microencapsulation effi ciency of 93.6 %. Temperature analysis showed that maltodextrin conferred protection up to 70 °C for 120 min. Scanning electron microscopy showed that the microencapsulated particles had a flake-like morphology with a smooth surface, characteristic of lyophilisation processes. In addition, when added to yogurt, a red colourant was predominant in the samples at pH from 1.5 up to 5.0. Thermal analysis showed a weak interaction between the sample and the encapsulating agent, and photoacoustic data indicated the photostability of the matrix when exposed to light. Yogurts containing microencapsulated anthocyanins showed a more intense pink colour than yogurts treated with pure dye, and sensory analysis demonstrated that they can have good acceptance on the market. Microencapsulation enabled the innovative application of anthocyanins from juçara palm fruit, and complementary techniques allied to the photoacoustic spectroscopy were effective tools for its evaluation.Antocijanini izolirani iz pulpe ploda palme Euterpe edulis Mart. enkapsulirani su maltodekstrinom radi poveÄanja njihove stabilnosti. Stabilnost mikrokapsula na svjetlu ispitana je pomoÄu fotoakustiÄne spektroskopije. Osim toga, kapsule su dodatno ispitane diferencijalnom pretraĆŸnom kalorimetrijom i pretraĆŸnom elektronskom mikroskopijom. Liofilizirani je ekstrakt sadrĆŸavao 14 340.2 mg/L ukupnih antocijanina, a uÄinkovitost postupka mikroenkapsulacije bila je 93,6 %. Toplinska je analiza potvrdila da maltodekstrin spreÄava razgradnju antocijanina na temperaturi do 70 ÂșC tijekom 120 min. PretraĆŸna je elektronska mikroskopija pokazala da su mikrokapsule imale pahuljastu strukturu i glatku povrĆĄinu, ĆĄto je tipiÄno za postupak liofilizacije. Osim toga, uzorci su jogurta kojima su dodane kapsule antocijanina pri pH-vrijednosti od 1,5 do 5,0 imali preteĆŸno crvenu boju. Toplinskom je analizom utvrÄeno da je doĆĄlo do slabog povezivanja uzorka s maltodekstrinom, a zatim je fotoakustiÄnom analizom ispitana stabilnost kapsula nakon izlaganja svjetlu. Jogurti s mikrokapsulama antocijanina imali su intenzivniju ruĆŸiÄastu boju od onih koji su sadrĆŸavali Äisto bojilo, a senzorska je analiza pokazala da su takvi proizvodi prihvatljivi na trĆŸiĆĄtu. Mikroenkapsulacija omoguÄuje novi naÄin primjene antocijanina iz ploda palme Euterpe edulis Mart., a za njihovu je procjenu moguÄe upotrijebiti fotoakustiÄnu spektroskopiju u kombinaciji s drugim metodama
CurcuminâÎČ-cyclodextrin inclusion complex: Stability, solubility, characterisation by FT-IR, FT-Raman, X-ray diffraction and photoacoustic spectroscopy, and food application
AbstractCurcumin was complexed with ÎČ-CD using co-precipitation, freeze-drying and solvent evaporation methods. Co-precipitation enabled complex formation, as indicated by the FT-IR and FT-Raman techniques via the shifts in the peaks that were assigned to the aromatic rings of curcumin. In addition, photoacoustic spectroscopy and X-ray diffraction, with the disappearance of the band related to aromatic rings, by Gaussian fitting, and modifications in the spectral lines, respectively, also suggested complex formation. The possible complexation had an efficiency of 74% and increased the solubility of the pure colourant 31-fold. CurcuminâÎČ-CD complex exhibited a sunlight stability 18% higher than the pure colourant. This material was stable to pH variations and storage at â15 and 4°C. With an isothermal heating at 100 and 150°C for 2h, the material exhibited a colour retention of approximately 99%. The application of curcuminâÎČ-CD complex in vanilla ice creams intensified the colour of the products and produced a great sensorial acceptance
Study of the chemical interaction between a high-viscosity glass ionomer cement and dentin
Objective: To investigate the chemical interactions between a high-viscosity glass ionomer cement (GIC) (KetacTM Molar Easymix, 3M ESPE, Seefeld, Bavaria, Germany) and human dentin. It was also analyzed the dynamics of GIC setting mechanism based on the time intervals required for the GIC and the GIC mixed with dentin to achieve stability. Material and Methods: Each constituent of GIC â powder (P) and liquid (L) â and powdered dentin (D), as well as the associations P+L, D+L, and P+L+D in the concentrations of 29%, 50%, 65%, 78%, 82%, and 92% of GIC were analyzed with Fourier transform infrared (FTIR) and Raman spectroscopy. Results: New optical absorption bands and/or Raman bands, which were not present in P, L, or D, were observed in the associations. The concentrations of 29% and 50% of GIC showed higher interaction, revealing that the amount of dentin influences the formation of new optical absorption or scattering bands. FTIR bands showed that the setting time to achieve bond stability was longer for the high-viscosity GIC (38±7 min) than for the sample with 29% of GIC (28±4 min). Conclusions: The analysis revealed the formation of new compounds or molecular rearrangements resulting from the chemical interactions between GIC and dentin. Moreover, this study provides an effective method to evaluate the dynamics of the setting mechanism of GICs
True absolute determination of photoluminescence quantum yields by coupling multiwavelength thermal lens and photoluminescence spectroscopies
© Royal Society of Chemistry 2020. This is the accepted manuscript version of an article which has been published in final form at https://dx.doi.org/10.1039/D0CP03794J.Photoluminescence quantum yields denote a critical variable to characterise a fluorophore and its potential performance. Their determination, by means of methodologies employing reference standard materials, innevitably leads to large uncertainties. In response to this, herein we report for the first time an innovative and elegant methodology, whereby the use of neat solvent/reference material required by thermal lens approaches is eliminated by coupling it to photoluminescence spectroscopy, allowing for the discrimination between materials with similar photoluminescence quantum yields. To achieve that, both radiative and non-radiative transitions are simultaneously measured by means of a photoluminescence spectrometer coupled to a multiwavelength thermal lens spectroscopy setup in a mode-mismatched dual-beam configuration, respectively. The absorption factor independent ratio of the thermal lens and photoluminescence signals can then be used to determine the fluorescence quantum yield both accurately and precisely. We validated our reported method by means of rhodamine 6G and further applied in three novel structurally related diketopyrrolopyrrole based materials to, contrary to results obtained by other methods, unveil significant differences in their photoluminescence quantum yields.Peer reviewe
Evaluation of the influence of light-curing units on the degree of conversion in depth of a bulk-fill resin
It is known that bulk-fill have been widely studied and used by dentists in the clinic. However, the use of light-curing units that do not have the ability to adequately light-cure these materials at the appropriate depth can affect their clinical perfor
Time-resolved thermal mirror technique with top-hat cw laser excitation.
A theoretical model was developed for time-resolved thermal mirror spectroscopy under top-hat cw laser excitation that induced a nanoscale surface displacement of a low absorption sample. An additional phase shift to the electrical field of a TEM(00) probe beam reflected from the surface displacement was derived, and Fresnel diffraction theory was used to calculate the propagation of the probe beam. With the theory, optical and thermal properties of three glasses were measured, and found to be consistent with literature values. With a top-hat excitation, an experimental apparatus was developed for either a single thermal mirror or a single thermal lens measurement. Furthermore, the apparatus was used for concurrent measurements of thermal mirror and thermal lens. More physical properties could be measured using the concurrent measurements
Analysis of energy transfer processes in 'Yb POT. 3+'-'Tb POT. 3+' co-doped, low-silica calcium aluminosilicate glasses
Energy transfer processes in Yb3+-Tb3+ co-doped, low-silica calcium aluminosilicate glasses were analyzed. Luminescence and time-resolved measurements were used to study upconversion processes, such as Yb-Tb cooperative sensitization, Yb-Yb cooperative luminescence, and Yb-Tb cross relaxation. The quantum cross relaxation efficiency was evaluated as a function on the Yb3+ concentration, and the maximum estimated value was approximately 51%. In addition, the intensity of the upconversion luminescence from the Tb3+:5D4 level decreased by two orders of magnitude comparing the value at room temperature with that at 123âK. As a consequence, Yb-Yb cooperative luminescence around 500 nm became comparable with the intensity of upconversion from the Tb3+:5D4 level. Furthermore, a dependence of the upconversion kinetics luminescence on temperature was observed. The upconversion rise time was constant and equal to 65âÎŒs for temperatures between 296 to 473âK and decreased from 65 to 19âÎŒs, without variation in the decay part, when the temperature was lowered from 296 to 123âK. These results were explained by a phonon-assisted cooperative sensitization process for the population of the Tb3+:5D4 level.CAPESINCT-INAM
Les droits disciplinaires des fonctions publiques : « unification », « harmonisation » ou « distanciation ». A propos de la loi du 26 avril 2016 relative à la déontologie et aux droits et obligations des fonctionnaires
The production of tt⟠, W+bb⟠and W+cc⟠is studied in the forward region of protonâproton collisions collected at a centre-of-mass energy of 8 TeV by the LHCb experiment, corresponding to an integrated luminosity of 1.98±0.02 fbâ1 . The W bosons are reconstructed in the decays WââÎœ , where â denotes muon or electron, while the b and c quarks are reconstructed as jets. All measured cross-sections are in agreement with next-to-leading-order Standard Model predictions.The production of , and is studied in the forward region of proton-proton collisions collected at a centre-of-mass energy of 8 TeV by the LHCb experiment, corresponding to an integrated luminosity of 1.98 0.02 \mbox{fb}^{-1}. The bosons are reconstructed in the decays , where denotes muon or electron, while the and quarks are reconstructed as jets. All measured cross-sections are in agreement with next-to-leading-order Standard Model predictions
Measurement of the (eta c)(1S) production cross-section in proton-proton collisions via the decay (eta c)(1S) -> p(p)over-bar
The production of the state in proton-proton collisions is probed via its decay to the final state with the LHCb detector, in the rapidity range GeV/c. The cross-section for prompt production of mesons relative to the prompt cross-section is measured, for the first time, to be at a centre-of-mass energy TeV using data corresponding to an integrated luminosity of 0.7 fb, and at TeV using 2.0 fb. The uncertainties quoted are, in order, statistical, systematic, and that on the ratio of branching fractions of the and decays to the final state. In addition, the inclusive branching fraction of -hadron decays into mesons is measured, for the first time, to be , where the third uncertainty includes also the uncertainty on the inclusive branching fraction from -hadron decays. The difference between the and meson masses is determined to be MeV/c.The production of the state in proton-proton collisions is probed via its decay to the final state with the LHCb detector, in the rapidity range . The cross-section for prompt production of mesons relative to the prompt cross-section is measured, for the first time, to be at a centre-of-mass energy using data corresponding to an integrated luminosity of 0.7Â fb , and at using 2.0Â fb . The uncertainties quoted are, in order, statistical, systematic, and that on the ratio of branching fractions of the and decays to the final state. In addition, the inclusive branching fraction of -hadron decays into mesons is measured, for the first time, to be , where the third uncertainty includes also the uncertainty on the inclusive branching fraction from -hadron decays. The difference between the and meson masses is determined to be .The production of the state in proton-proton collisions is probed via its decay to the final state with the LHCb detector, in the rapidity range GeV/c. The cross-section for prompt production of mesons relative to the prompt cross-section is measured, for the first time, to be at a centre-of-mass energy TeV using data corresponding to an integrated luminosity of 0.7 fb, and at TeV using 2.0 fb. The uncertainties quoted are, in order, statistical, systematic, and that on the ratio of branching fractions of the and decays to the final state. In addition, the inclusive branching fraction of -hadron decays into mesons is measured, for the first time, to be , where the third uncertainty includes also the uncertainty on the inclusive branching fraction from -hadron decays. The difference between the and meson masses is determined to be MeV/c
Search for the lepton flavour violating decay tau(-) -> mu(-)mu(+)mu(-)
A search for the lepton flavour violating decay is performed with the LHCb experiment. The data sample corresponds to an integrated luminosity of 1.0 fb of proton-proton collisions at a centre-of-mass energy of 7 TeV and 2.0 fb at 8 TeV. No evidence is found for a signal, and a limit is set at 90% confidence level on the branching fraction, .A search for the lepton flavour violating decay Ï â ÎŒ ÎŒ ÎŒ is performed with the LHCb experiment. The data sample corresponds to an integrated luminosity of 1.0 fb of proton-proton collisions at a centre-of-mass energy of 7 TeV and 2.0 fb at 8 TeV. No evidence is found for a signal, and a limit is set at 90% confidence level on the branching fraction, .A search for the lepton flavour violating decay is performed with the LHCb experiment. The data sample corresponds to an integrated luminosity of of proton-proton collisions at a centre-of-mass energy of and at . No evidence is found for a signal, and a limit is set at confidence level on the branching fraction,
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