On the novel free porphyrins corallistin B, C, D, and E : isolation from the demosponge Corallistes sp. of the Coral Sea and reactivity of their nickel (2) complexes toward formylating reagents

Reported here are the novel free corallistin B, C, D, and E, isolated as methyl esters 2a, 3a, 4a, and 5a, respectively, from the sponge #Corallistes sp.(#Lithistida) collected at the basis of the South New Caledonian coral reef. A protocol is also established for formulation of their NiII complexes, which show a different reactivity pattern toward DMF/POCI3 from metal complexes of deuteroporphyrin IX (isolate as 6a) also present in the sponge, the new corallistins, which may be thought to derive from protoporphyrin via heme, account for an amazing 60% of the etOH extract from the sponge. (Résumé d'auteur

\u3cem\u3eMycobacterium marinum\u3c/em\u3e Infection After Exposure to Coal Mine Water

Mycobacterium marinum infection has been historically associated with exposure to aquariums, swimming pools, fish, or other marine fauna. We present a case of M marinum left wrist tenosynovitis and elbow bursitis associated with a puncture injury and exposure to coal mine water in Illinois

The Dynamic Formation of Prominence Condensations

We present simulations of a model for the formation of a prominence condensation in a coronal loop. The key idea behind the model is that the spatial localization of loop heating near the chromosphere leads to a catastrophic cooling in the corona (Antiochos & Klimchuk 1991). Using a new adaptive grid code, we simulate the complete growth of a condensation, and find that after approx. 5,000 s it reaches a quasi-steady state. We show that the size and the growth time of the condensation are in good agreement with data, and discuss the implications of the model for coronal heating and SOHO/TRACE observations.Comment: Astrophysical Journal latex file, 20 pages, 7 b-w figures (gif files

Effect of Dendritic Side Groups on the Mobility of Modified Poly(epichlorohydrin) Copolymers

[EN] The macromolecular dynamics of dendronized copolymer membranes (PECHs), obtained by chemical modification of poly(epichlorohydrin) with the dendron 3,4,5-tris[4-(n-dodecan-1-yloxy)benzyloxy] benzoate, was investigated. In response to a thermal treatment during membrane preparation, these copolymers show an ability to change their shape, achieve orientation, and slightly crystallize, which was also observed by CP-MAS NMR, XRD, and DSC. The phenomenon was deeply analyzed by dielectric thermal analysis. The dielectric spectra show the influence of several factors such as the number of dendritic side groups, the orientation, their self-assembling dendrons, and the molecular mobility. The dielectric spectra present a sub-Tg dielectric relaxation, labelled as gamma, associated with the mobility of the benzyloxy substituent of the dendritic group. This mobility is not related to the percentage of these lateral chains but is somewhat hindered by the orientation of the dendritic groups. Unlike other less complex polymers, the crystallization was dismantled before the appearance of the glass transition (alpha(Tg)). Only after that, clearing transition (alpha(Clear)) can be observed. The PECHs were flexible and offered a high free volume, despite presenting a high degree of modifications. However, the molecular mobility is not independent in each phase and the self-assembling dendrons can be eventually fine-tuned according to the percentage of grafted groups.This research was funded by the Spanish Ministry of Science, Innovation and Universities, grant POLYDECARBOCELL (ENE2017-86711-C3-1-R, ENE2017-86711-C3-3-R).Teruel Juanes, R.; Pascual-Jose, B.; Graf, R.; Reina, JA.; Giamberini, M.; Ribes-Greus, A. (2021). Effect of Dendritic Side Groups on the Mobility of Modified Poly(epichlorohydrin) Copolymers. Polymers. 13(12):1-19. https://doi.org/10.3390/polym13121961119131

Agelastatin A, a new skeleton cytotoxic alkaloid of the oroidin family : isolation from the Axinellid sponge Agelas dendromorpha of the Coral Sea

Agelastatin A, isolated from the axinellid sponge #Agelas dendromorpha$ of the Coral Sea, is a new skeleton alkaloid with, unusually for the oroidin family to which it belongs, marked cytototoxicity toward tumour cells in culture. (Résumé d'auteur

Degradation of Plasticised Poly(lactide) Composites with Nanofibrillated Cellulose in Different Hydrothermal Environments

In this study, bionanocomposite films based on poly(lactide) (PLA) plasticised with poly(ethylene glycol) (PEG) (7.5 wt%) and reinforced with various contents of nanofibrillated cellulose (NFC) (1, 3, 5 wt%) were prepared. The hydrothermal degradation was investigated through immersion in several aqueous environments at temperatures of 8, 23, 58, and 70 °C as a function of time (7, 15, 30, 60, 90 days). The effect of water immersion on the physicochemical properties of the materials was assessed by monitoring the changes in the morphology, thermo-oxidative stability, thermal properties, and molar mass through field emission scanning electron microscopy (FE-SEM), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and gel permeation chromatography (GPC). The hydrothermal degradation behaviour was not critically affected regardless of the nanofibrillated cellulose content. All the materials revealed certain integrity towards water immersion and hydrolysis effects at low temperatures (8 and 23 °C). The low hydrothermal degradation may be an advantage for using these PLA biocomposites in contact with water at ambient temperatures and limited exposure times. On the other hand, immersion in water at higher temperatures above the glass transition (58 and 70 °C), leads to a drastic deterioration of the properties of these PLA-based materials, in particular to the reduction of the molar mass and the disintegration into small pieces. This hydrothermal degradation behaviour can be considered a feasible option for the waste management of PLA/PEG/NFC bionanocomposites by deposition in hot aqueous environments

Structure–Properties Relationship of Reprocessed Bionanocomposites of Plasticized Polylactide Reinforced with Nanofibrillated Cellulose

Bionanocomposites of polylactide (PLA), plasticized with poly(ethylene glycol) (PEG) (7.5 wt%, 400 and 1500 g/mol) and reinforced with nanofibrillated cellulose (NFC) (1, 3, and 5 wt%) were sequentially compounded, and injection and compression molded. All of the stages caused structural and morphological consequences, more relevant in the plasticized PLA, especially with low molar PEG. Small percentages of NFC (1 and 3 wt%) acted as crystalline nucleating agents and improved thermo-oxidative stability. Given the substantial degradation caused by (re)processing, a downgrading validation strategy was applied, assessing the mechanical and water contact performance during fictional first and second service life applications. After the first processing, PEG increased the ductility and reduced the strength and elastic modulus, while NFC buffered the fall in stiffness and increased rigidity compared to their PLA-PEG counterparts. Once reprocessed, PEG increased the water affinity of the blend, especially for low molar mass PEG. Low percentages of NFC (1 and 3 wt%) modulated water diffusivity and permeability, regardless of the water temperature. Overall, although reprocessing caused significant degradation, the mechanical valorization possibilities of these green bionanocomposites were proven, and are pointed out as sustainable candidates for food packaging or agricultural applications where modulated mechanical or water contact behaviors are required

Experimental investigation of SO2 poisoning in a Molten Carbonate Fuel Cell operating in CCS configuration

[EN] One of the most interesting innovations in the CCS (Carbon Capture and Storage) field is the use of MCFCs as carbon dioxide concentrators, feeding their cathode side (or air side) with the exhaust gas of a traditional power plant. The feasibility of this kind of application depends on the resistance of the MCFC to air-side contaminants, with particular attention to SO2. The aim of this work is to investigate the effects of poisoning when sulphur dioxide is added to the cathodic stream in various concentrations and in different operating conditions. This study was carried out operating single cells (80 cm(2)) with a cathodic feeding composition simulating typical flue gas conditions, i.e. N-2, H2O, O-2 and CO2 in 73:9:12:6 mol ratio as reference mixture. On the anodic side a base composition was chosen with H-2, CO2 and H2O in 64:16:20 mol ratio. Starting from these reference mixtures, the effect of single species on cell poisoning was experimentally investigated considering, as main parameters chosen for the sensitivity analysis, SO2 (0-24 ppm) and CO2 (4-12%) content in the cathodic feeding mixture, H-2 (40-64%) content in the anodic stream as well as the operating temperature (620-680 degrees C). Results showed that degradation caused by SO2 poisoning is strongly affected by the operating conditions. Data gathered during this experimental campaign will be used in a future work to model the poisoning mechanisms through the definition of MCFC electrochemical kinetics which take into account the SO2 effects. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.The work was partly supported by H2FC European Infrastructure Project (Integrating European Infrastructure to support science and development of Hydrogen and Fuel Cell Technologies towards European Strategy for Sustain-able Competitive and Secure Energy) Theme [INFRA-2011-1.1.16.], Grant agreement 284522.Della Pietra, M.; Discepoli, G.; Bosio, B.; Mcphail, S.; Barelli, L.; Bidini, G.; Ribes-Greus, A. (2016). Experimental investigation of SO2 poisoning in a Molten Carbonate Fuel Cell operating in CCS configuration. International Journal of Hydrogen Energy. 41(41):18822-18836. https://doi.org/10.1016/j.ijhydene.2016.05.147S1882218836414