Report on advances for pediatricians in 2018: allergy, cardiology, critical care, endocrinology, hereditary metabolic diseases, gastroenterology, infectious diseases, neonatology, nutrition, respiratory tract disorders and surgery.

This review reported notable advances in pediatrics that have been published in 2018. We have highlighted progresses in allergy, cardiology, critical care, endocrinology, hereditary metabolic diseases, gastroenterology, infectious diseases, neonatology, nutrition, respiratory tract disorders and surgery. Many studies have informed on epidemiologic observations. Promising outcomes in prevention, diagnosis and treatment have been reported. We think that advances realized in 2018 can now be utilized to ameliorate patient car

Partial Hydrogenation of Soybean and Waste Cooking Oil Biodiesel over Recyclable-Polymer-Supported Pd and Ni Nanoparticles

Biodiesel obtained through the transesterification in methanol of vegetable oils, such as soybean oil (SO) and waste cooking oil (WCO), cannot be used as a biofuel for automotive applications due to the presence of polyunsaturated fatty esters, which have a detrimental effect on oxidation stability (OS). A method of upgrading this material is the catalytic partial hydrogenation of the fatty acid methyl ester (FAME) mixture. The target molecule of the partial hydrogenation reaction is monounsaturated methyl oleate (C18:1), which represents a good compromise between OS and the cold filter plugging point (CFPP) value, which becomes too high if the biodiesel consists of unsaturated fatty esters only. In the present work, polymer-supported palladium (Pd-pol) and nickel (Ni-pol) nanoparticles were separately tested as catalysts for upgrading SO and WCO biodiesels under mild conditions (room temperature for Pd-pol and T = 100◦ C for Ni-pol) using dihydrogen (p = 10 bar) as the reductant. Both catalysts were obtained through co-polymerization of the metal containing monomer M(AAEMA)2 (M = Pd, Ni; AEEMA− = deprotonated form of 2-(acetoacetoxy)ethyl methacrylate)) with co-monomers (ethyl methacrylate for Pd and N,N-dimethylacrilamide for Ni) and cross-linkers (ethylene glycol dimethacrylate for Pd and N,N’-methylene bis-acrylamide for Ni), followed by reduction. The Pd-pol system became very active in the hydrogenation of C=C double bonds, but poorly selective towards the desirable C18:1 product. The Ni-pol catalyst was less active than Pd-pol, but very selective towards the mono-unsaturated product. Recyclability tests demonstrated that the Ni-based system retained its activity and selectivity with both the SO and WCO substrates for at least five subsequent runs, thus representing an opportunity for waste biomass valorization

Microwave-Assisted Treatment of Waste Wood Biomass with Deep Eutectic Solvents

Abstract. The increasing depletion of fossil feeds and the environmental concerns linked to the use of traditional energy sources have stimulated both academic and industrial worlds in exploiting new sustainable and renewable suppliers of raw materials [1]. In this framework, lignocellulosic biomass can play an important role, acting as the starting material of a biorefinery leading to biofuels, chemicals, and other value-added products, commonly obtained from petroleum. Recently, numerous protocols for processing lignocellulosic biomass of selected plants have been reported. However, developing an environment-friendly method is still a big goal. This challenge becomes more interesting if lignocellulosic biomass coming from wood wastes could be efficiently treated. Deep eutectic solvents (DESs) are new sustainable and cheap reaction media, combining the features of ionic liquids and organic solvents. They are made by association of hydrogen-bond donors and hydrogen-bond acceptors, and they can promote the hydrolysis of lignocellulosic bonds [2]. Herein, we report on the microwave-assisted treatment of waste wood flours with DESs formed by choline chloride and oxalic acid to get a cellulosic residue separated from lignin degradation products, identified by NMR spectroscopy. The insoluble deposit was characterized by SEM, TGA, DSC, FTIR-ATR and 13C CP/MAS NMR techniques and could be available for further uses such as nanocellulose production. [1] Haldar D., Purkait M.K. Chemosphere 2021, 128523. [2] Liu S., Zhang Q., Gou S., Zhang L., Wang Z. Carbohydr. Polym. 2021, 251, 11701

. Microwave-assisted solvothermal controlled synthesis of Fe-Co

Syntheses of bimetallic cobalt-iron-based nanoparticles starting from Co(acac)2 and Fe(acac)3 (acac = acetylacetonate) were carried out by microwave-assisted solvothermal process, using ethylene glycol as the solvent and (polyvinylpyrrolidone) PVP, as the stabilizer. Indeed, the reaction mechanism in the presence of ethylene glycol is well understood [1] with the role of PVP being the inhibition of nanoparticles growth [2]. However, the control of the morphology of the synthetized nanoparticles is still a great challenge. Herein, we demonstrated that by adding amines to the reaction mixture, it is possible to control the morphology of the prepared bimetallic cobalt-iron materials. Thus, different Co-Fe micro-composites were synthetized by an innovative microwave assisted solvothermal synthesis, which allows to considerably reduce reaction time from 12 h to 15 min, with respect to classical thermal methods. The procedure was optimized by varying several parameters, such as: amount of PVP, in the presence or in the absence of amines, reaction temperature. The dark brown obtained powders were characterized by scanning electron microscopy, infrared spectroscopy and thermogravimetric analysis, confirming the beneficial effect of the presence of the amine in the morphology of the obtained composites. The obtained results open a new scenario for further studies on the possibility to control the morphology of bimetallic composite materials. [1] Fievet F, Lagier J P and Figlarz M Mater. Res. Soc. Bull. 24 (1989) 29–34 [2] Teranishi T, Kurita R and Miyake M J. Inorg. Organometall. Polym. 10 (2000) 145–5

Risk of infectious mononucleosis among agonistic swimmers: a cross-sectional study

BACKGROUND: The risk of infectious mononucleosis among athletes is quite debated. Some personal observations seem to suggest an increase risk of mononucleosis among athletes, because they attend always close settings with an high probability of respiratory pathogens transmission; overtraining has been also proposed as risk factor. STUDY DESIGN: Cross-sectional study in a group of swimmers (aged 11-14 years) of the University Sport Centre of Bari. METHODS: 40 swimmers were interviewed by healthcare personnel at the end of training courses; demographic characteristics, personal habits, information about sport training and diagnosis of mononucleosis were analysed. RESULTS: The life-time incidence of mononucleosis was around 40%; multivariate analysis showed the association between mononucleosis and use of bottles of other persons (aOR=8.2; 95% CI=1.4-49.2; z=2.32; p=0.021) and average duration of training session was longer among subjects who reported mononucleosis than in subjects who did not indicate this disease. CONCLUSIONS: Future multi-centric studies are needed to better define the epidemiology of the mononucleosis in sport settings and to formulate appropriate recommendations to prevent the spreading of this disease

Synthesis and activity of -Fe2O3 nanoparticles in the catalytic reduction of halonitroarenes under sustainable conditions

Abstract. The catalytic reduction of nitroarenes towards anilines is an important reaction from both academic and industrial points of view, being the resulting products important intermediates to produce dyes, agrochemicals, pigments, and pharmaceuticals. In addition, removal of nitroarene pollutants from water by reducing them into anilines is a valuable method to purify contaminated matrices. Such reductive reactions are frequently carried out by using noble metal catalysts [1], which are usually very active and recyclable in some cases. Recently, the use of earth abundant metal catalysts has gained great interest especially for economic reasons, as these materials are generally cheap and easy to be reached [2]. In this framework, iron oxides catalysts are very attractive because they are cheap and not toxic. Herein, we report on the synthesis of α-Fe2O3 nanoparticles (NPs) of size ranging from 50 to 80 nm starting from a porous organic polymer (POP) containing Fe(III) sites, which was in turn annealed at 400°C. The obtained NPs were characterized by SEM-EDX, XRPD, IR and TXRF and were employed as active and recyclable catalysts in the reduction of p-bromonitrobenzene into p-bromo-aniline, using hydrazine hydrate in ethanol, taken as the model reaction. [1] Dell’Anna, M.M.; Intini, S.; Romanazzi, G.; Rizzuti, A.; Leonelli, C.; Piccinni, F.; Mastrorilli, P. J. Mol. Catal. A: Chem. 2014, 395, 307–314. [2] Romanazzi, G.; Fiore, A.M.; Mali, M.; Rizzuti, A.; Leonelli, C.; Nacci, A.; Mastrorilli, P.; Dell'Anna, M. M. Mol. Catal., 2018, 446, 31–3

The role of parental involvement in youth sport experience: perceived and desired behavior by male soccer players

Parents play a key role in the youth sports educational experience. They are responsible for the introduction of their children to physical or sporting education and their involvement has been associated with sport participation in early stages. The aims of this cross-sectional study were, first, to assess the perceived and desired parental involvement by children and, secondly, to exam-ine their satisfaction or dissatisfaction with any specific behavior. 80 male soccer players filled the Parental Involvement in Sport Questionnaire (PISQ) before or after a training session in presence of a coach. PISQ results revealed excessive active involvement and pressure, insufficient praise and understanding and satisfactory directive behavior from children’s parents. Our findings suggest that excessive parental involvement can cause pressure on children who would prefer parental participation characterized by praise and understanding. A balance between a supporting involvement without putting too much pressure is needed by the parents. To prevent burnout and dropout and to facilitate future practice, parents should be counseled (possibly by a sport educator) on how to positively support their children concerning their sport experience

Synthesis of Fe2O3 Nanoparticles and their Catalytic Activity for the Reduction of Halonitroarenes under Sustainable Conditions

Fe2O3 nanoparticles (NPs) with mean size of 50 nm ca. are synthesized starting from a porous organic polymer containing beta-ketoesterate Fe(III) sites (Fe-POP), which is annealed at 400 degrees C under air for 30 min. During calcination, the organic material partially decomposes, and iron(III) oxide NPs onto an organic residue could be observed after annealing. The obtained NPs are characterized by SEM-EDS, IR, and magnetic analyses and they are employed as active catalysts in the reduction of p-bromonitrobenzene into p-bromoaniline, using hydrazine hydrate in ethano

Polyacetylenes Bearing Chiral-Substituted Fluorene and Terfluorene Pendant Groups: Synthesis and Properties

The synthesis of the first polyacetylenes bearing chiral fluorene-based pendant groups is described. Poly{9,9-bis[(S)-3,7-dimethyloctyl]fluoren-2-ylacetylene} (PFA1), poly{9,9-bis[(S)-2-methylbutyl]- fluoren-2-ylacetylene} (PFA2), and poly{9,9,9′,9′,9′′,9′′-hexakis[(S)-2-methylbutyl]-7,2′;7′,2′′-terfluoren- 2-ylacetylene} (PFA3) have been obtained by Rh(I)-catalyzed polymerization of the corresponding terminal acetylene monomers 2-ethynyl-9,9-bis[(S)-3,7-dimethyloctyl]fluorene (2a), 2-ethynyl-9,9-bis[(S)-2-methylbutyl]fluorene (2b), and 2-ethynyl-9,9,9′,9′,9′′,9′′-hexakis[(S)-2-methylbutyl]-7,2′;7′,2′′-terfluorene (10). The effect of the alkyl chain length at the C-9 position of fluorene on the structural and conformational aspects of the polymers PFA1 and PFA2 as well as on their chiroptical properties was studied by XRD, DSC, TGA, GPC, UV-vis, and CD. A more planar conformation of the polyenic backbone of PFA1 with respect to PFA2 can be inferred by a red shift of the ð-ð* transition in the UV-vis spectra. Their photoluminescence properties are those typical of fluorene systems. CD measurements evidenced Cotton effects of opposite signs in correspondence of the backbone absorption region, ascribable to an excess of a screw sense of the helical conformations assumed by the two polymers. PFA3 revealed an amorphous structure and exhibited peculiar thermal stability features (as indicated by TGA and DSC). Its emission spectra interest the violet-blue region and do not show any substantial red shift passing from solution to solid state, thus pointing out an aggregation prevention of terfluorene groups by means of the polyacetylene backbone