New insights in Microbial Fuel Cells: Novel solid phase anolyte

For the development of long lasting portable microbial fuel cells (MFCs) new strategies are necessary to overcome critical issues such as hydraulic pump system and the biochemical substrate retrieval overtime to sustain bacteria metabolism. The present work proposes the use of a synthetic solid anolyte (SSA), constituted by agar, carbonaceous and nitrogen sources dissolved into diluted seawater. Results of a month-test showed the potential of the new SSA-MFC as a long lasting low energy consuming system

A short review of green extraction technologies for rice bran oil

Rice is one of the most important crops throughout the world, as it contributes toward satisfying the food demand of much of the global population. It is well-known that rice production generates a considerable number of by-products, among which rice bran deserves particular attention. This by-product is exceptionally rich in nutrients, since it contains a wide spectrum of macronutrients (proteins, fats, carbohydrates) as well as dietary fibers and bioactive compounds. However, rice bran is usually wasted or just used for the production of low-cost products. The lipidic fraction of rice bran contains an unsaponifiable fraction that is rich in such functional components as tocopherols, γ-oryzanol, tocotrienols and phytosterols. This lipidic fraction can be extracted to obtain rice bran oil (RBO), a high value-added product with unique health properties as a result of its high concentration in γ-oryzanol, a powerful antioxidant mixture of bioactive molecules. Conventional extraction methods employ hexane as the solvent, but these methods suffer from some drawbacks linked to the toxicity of hexane for humans and the environment. The aim of the review presented herein is to point out the new green technologies currently applied for the extraction of RBO, by highlighting reliable alternatives to conventional solvent extraction methods that are in line with the twelve principles of green chemistry and a circular economy

Electrochemical and impedance characterization of Microbial Fuel Cells based on 2D and 3D anodic electrodes working with seawater microorganisms under continuous operation

A mixed microbial population naturally presents in seawater was used as active anodic biofilm of two Microbial Fuel Cells (MFCs), employing either a 2D commercial carbon felt or 3D carbon-coated Berl saddles as anode electrodes, with the aim to compare their electrochemical behavior under continuous operation. After an initial increase of the maximum power density, the felt-based cell reduced its performance at 5months (from 7 to 4μWcm(-2)), while the saddle-based MFC exceeds 9μWcm(-2) (after 2months) and maintained such performance for all the tests. Electrochemical impedance spectroscopy was used to identify the MFCs controlling losses and indicates that the mass-transport limitations at the biofilm-electrolyte interface have the main contribution (>95%) to their internal resistance. The activation resistance was one order of magnitude lower with the Berl saddles than with carbon felt, suggesting an enhanced charge-transfer in the high surface-area 3D electrode, due to an increase in bacteria population growth

Additive Manufacturing of a Microbial Fuel Cell - A detailed study

In contemporary society we observe an everlasting permeation of electron devices, smartphones, portable computing tools. The tiniest living organisms on Earth could become the key to address this challenge: energy generation by bacterial processes from renewable stocks/waste through devices such as microbial fuel cells (MFCs). However, the application of this solution was limited by a moderately low efficiency. We explored the limits, if any, of additive manufacturing (AM) technology to fabricate a fully AM-based powering device, exploiting low density, open porosities able to host the microbes, systems easy to fuel continuously and to run safely. We obtained an optimal energy recovery close to 3 kWh m−3 per day that can power sensors and low-power appliances, allowing data processing and transmission from remote/harsh environments

Recycling CO2from flue gas for CaCO3nanoparticles production as cement filler: A Life Cycle Assessment

CaCO3 nanoparticles as filler have received considerable attention for the mechanical improvement that they provide to cements. However, their life-cycle impact on the environment remains almost unexplored, even if the cement industry is considered one of the largest CO2 emitters. In this perspective, this research work assessed a novel method for using CO2 from cement flue gases to produce nanoCaCO3 as cement filler within the cradle to cradle thinking. For this purpose, two routes of CO2 capture were assessed followed by the study of the synthesis of CaCO3 through a mineral carbonation. Three scenarios for the synthesis of CaCO3 nanoparticles were assessed targeting the use of waste or by-products as raw materials and recirculation of them to reduce any kind of emission. The three scenarios were evaluated by means of the Life Cycle Assessment methodology. Once the best considered route for nanoCaCO3 production was determined, this research work examined the environmental effect of including 2 wt% of CaCO3 nanoparticles into the cement. Closing the loop follows a circular economy approach since the CO2 is captured within the same cement factory. The results were compared with conventional Portland cement. Regarding nanoCaCO3 results, the scenario with simultaneous production of NH4Cl, and using as calcium source CaCl2 deriving from the soda ash Solvay process, proved to be the best option. Moreover, when cement was filled with 2 wt% of this nanoCaCO3, the benefit in terms of emission reductions in the Climate Change category was higher than 60 % compared to the conventional Portland cement.This project has received funding from the European Union's Horizon 2020 Research and Innovation Programme under Grant Agreement No. 768583- RECODE project (Recycling carbon dioxide in the cement industry to produce added-value additives: a step towards a CO2 circular economy, https://www.recodeh2020.eu/). This paper reflects only the author's view and the content is the sole responsibility of the authors. The European Commission or its services cannot be held responsible for any use that may be made of the information it contains.Publicad

Modification and characterization of clinoptilolite for the co-immobilization of formate dehydrogenase and glycerol dehydrogenase enzymes

In the last decades there is a rising concern for the increasing concentration of carbon dioxide, considered the major responsible of Global Warming. A solution to this critical issue is the catalytic conversion of CO2 into high value-added products. Among the different strategies that could be applied, the enzymatic process of CO2 reduction to methanol, employing a sequence of three enzyme-catalyzed reactions, seems to be very promising. The simultaneous employment of formate dehydrogenase and glycerol dehydrogenase allows to reduce CO2 to formic acid, the first of the sequential reactions, and at the same time regenerate the nicotinamide cofactor, that is very expensive. To reuse enzymes, with a consequential reduction of cost, and increased their stability, they can be immobilized on a proper support. In this context, porous materials, such as zeolites, present appropriate features to be suitable for enzymes immobilization. In particular, they are well suited for the covalent immobilization technique due to the fact that they can be functionalized with different functional groups. Natural zeolites, like Clinoptilolite have the advantage to be low-cost materials largely diffused in different part of the world. Clinoptilolite was subjected to dealumination-desilication treatments to modify the zeolite’s morphology, increasing its specific surface area. According to the literature, the dealumination procedure was done with sequential acid attacks using HCl solutions. Instead, for the subsequent desilication process NaOH solution is required. The effects of desilication-dealumination treatments were investigated through complementary techniques such as N2 physisorption at -196 °C, XRD and SEM. The analysis revealed that the Clinoptilolite specific surface area increased by 400% following the dealumination-desilication procedure; at the same time the XRD analysis shows that the processed Clinoptilolite has the same main peaks of the unmodified one. Finally, the retained activity and the stability of the immobilized enzymes were evaluated, the results show that these aspects were enhanced by the modification through acid-alkaline attacks of the Clinoptilolite