Water splitting by MnFe2O4/Na2CO3 reversible redox reactions

Future energy systems must call upon clean and renewable sources capable of reducing associated CO₂ emissions. The present research opens new perspectives for renewable energy-based hydrogen production by water splitting using metal oxide oxidation/reduction reactants. An earlier multicriteria assessment defined top priorities, with MnFe₂O₄/Na₂CO₃/H₂O and Mn₃O₄/MnO/NaMnO₂/H₂O multistep redox cycles having the highest potential. The latter redox system was previously assessed and proven difficult to be conducted. The former redox system was hence experimentally investigated in the present research at the 0.5 to 250 g scale in isothermal thermogravimetry, an electrically heated furnace, and a concentrated solar reactor. Over 30 successive oxidation/reduction cycles were assessed, and the H₂ production efficiencies exceeded 98 % for the coprecipitated reactant after these multiple cycles. Tentative economics using a coprecipitated reactant revealed that 120 cycles are needed to achieve a 1 € per kg H₂ cost. Improving the cheaper ball-milled reactant could reduce costs by approximately 30 %. The initial results confirm that future research is important.

Investigating H₂ production by MnFe₂O₄/Na₂CO₃/H₂O redox cycles, using different reactants. Using the more efficient coprecipitated reactant, production costs will be ∼1€ per kg H₂, if 120 cycles are achieved. Improving the cheaper ball-milled reactant is recommended.     

Novel Chronic Anaplasmosis in Splenectomized Patient,Amazon Rainforest

We report a case of unusual human anaplasmosis in the Amazon rainforest of French Guiana. Molecular typing demonstrated that the pathogen is a novel Anaplasma species, distinct to all known species, and more genetically related to recently described Anaplasma spp. causing infections in rainforest wild fauna of Brazil.     

A Slight Adjustment of the Nutri-Score Nutrient Profiling System Could Help to Better Reflect the European Dietary Guidelines Regarding Nuts

The consumption of nuts remains low among European populations despite widespread inclusion as a recommended food group across European dietary guidelines. Front-of-Pack nutrition labelling systems are designed to support consumers make healthier choices and to stimulate product improvement, thus representing a pivotal opportunity to reduce the gap between intakes and recommendations. This study examined how the Nutri-Score algorithm treats nuts and nut-containing products and tested whether slight adjustments could better recognise and motivate nut inclusion in foods and diets. The nutritional score (ScN) and corresponding Nutri-Score letter of 68 nuts and nut-containing products were calculated, using the initial algorithm and slight adjustments, where nut weight was doubled (S1), saturated fats (S2) or energy (S3) from nuts were discounted, or saturated fats were replaced by the saturated fats/lipid ratio (S4). The correlation between the nuts’ content and the ScN was moderate for the initial algorithm (R² = 0.34) and S1 (R² = 0.36), but improved for S2, S3 and S4 (R² = 0.54, 0.55 and 0.52, respectively). Four plain nuts, initially labelled as “B” or “C” obtained a Nutri-Score “A” with S2, S3 and S4. Slight adjustments could better align the Nutri-Score with food-based dietary guidelines, reassure consumers on healthfulness of nuts and nut-containing products, whilst incentivising the inclusion of nuts in diverse foods.     

A High Proliferation Rate is Critical for Reproducible and Standardized Embryoid Body Formation from Laminin-521-Based Human Pluripotent Stem Cell Cultures

When aiming for homogenous embryoid body (EB) differentiation, the use of equal-sized EBs is required to avoid a size-induced differentiation bias. In this study we developed an efficient and standardized EB formation protocol for human pluripotent stem cells (hPSC) cultured in a laminin-521-based xeno-free system. As the cell proliferation rate of the cells growing on laminin-521 strongly affected the efficiency of aggregate formation, we found that recently passaged cells, as well as the addition of ROCK inhibitor, were essential for reproducible EB formation from hPSC single-cell suspensions. EBs could be obtained in a variety of differentiation media, in 96-well round-bottom plates and in hanging drops. Gene expression studies on differentially sized EBs from three individual human embryonic stem cell lines demonstrated that the medium used for differentiation influenced the differentiation outcome to a much greater extent than the number of cells used for the initial EB formation. Our findings give a new insight into factors that influence the EB formation and differentiation process. This optimized method allows us to easily manipulate EB formation and provide an excellent starting point for downstream EB-based differentiation protocols.