Corn Cobs' Biochar as Green Host of Salt Hydrates for Enhancing the Water Sorption Kinetics in Thermochemical Heat Storage Systems.

Heat storage technologies are essential for increasing the use of solar energy in the household sector. Their development can be achieved by designing new storage materials; one way is to impregnate a porous matrix with hygroscopic salts. In this article, the possibility of using biochar-based composite sorbents to develop promising new heat storage materials for efficient thermal storage is explored. Biochar-based composites with defined salt loadings (5, 10, 15, and 20%) were produced by impregnating MgSO4 into a biochar matrix derived from corn cobs. The new materials demonstrated a high water sorption capacity of 0.24 g/g (20MgCC). After six successive charging-discharging cycles (dehydration/dehydration cycles), only a negligible variation of the heat released and the water uptake was measured, confirming the absence of deactivation of 20MgCC upon cycling. The new 20MgCC composite showed an energy storage density of 635 J/g (Tads = 30 °C and RH = 60%), higher than that of other composites containing a similar amount of hydrate salt. The macroporous nature of this biochar increases the available surface for salt deposition. During the hydration step, the water molecules effectively diffuse through a homogeneous layer of salt, as described by the intra-particle model applied in this work. The new efficient biochar-based composites open a low-carbon path for the production of sustainable thermal energy storage materials and applications.

Tomato waste biochar in the framework of circular economy.

Tomato pomace was slowly pyrolyzed at 350 and 550 °C (under an N2 flow of 50 L/h) at a rate of 6 °C/min and a residence time of 1:30 h to produce two biochars named B350 and B550, respectively. In addition, the two biochars were chemically activated with ΚΟΗ (at a ratio of 1:10 w/v) at 800 °C to produce two new materials named BA350 and BA550. The four biochars produced were characterized physically and chemically (pH, yield, calorific value). They were also analyzed by scanning electron microscopy (SEM), Brunauer-Emmett-Teller (B.E.T), elemental analysis (EA), and thermogravimetric analysis (TGA). The results showed that as the pyrolysis temperature increased (350 to 550 °C), the specific surface area (SSA) increased. The latter was also significantly increased by the activation process. EA showed a variation in the mineral content of the produced biochars, resulting in a different content of the biochars after activation. The parameters studied showed that biochars from tomato waste could be used as an organic amendment to improve soil fertility in agricultural. In addition, because of their ability to absorb water, they could be used as a water reservoir in soils in arid areas.

Numerical Modeling in Membrane Processes.

Membrane processes have demonstrated their enormous potential for water treatment, either by removing organic and mineral contaminants before permeating stream discharge, or by concentrating high added-value compounds in retentate stream [...].

A Novel Numerical Procedure to Estimate the Electric Charge in the Pore from Filtration of Single-Salt Solutions.

The assessment of physicochemical parameters governing the transport of ions through nanoporous membranes is a major challenge due to the difficulty in experimental estimation of the dielectric constant of the solution confined in nanopores and the volumetric membrane charge. Numerical identification by adjusting their values to fit experimental data is a potential solution, but this method is complicated for single-salt solutions due to the infinite number of couples that can describe a rejection curve. In this study, a novel procedure based on physical simplifications which allows the estimation of a range of values for these two parameters is proposed. It is shown here that the evolution of the interval of membrane charge with salt concentration can be described in all the experimental conditions by the Langmuir-Freundlich hybrid adsorption isotherm. Finally, it is highlighted that considering the mean dielectric constant and the adsorption isotherms assessed from a range of concentrations allowed a good prediction of rejection curves, irrespective of the salt and membrane considered.

Study of the relationship between applied transmembrane pressure and antimicrobial activity of lysozyme.

During the processing of biomolecules by ultrafiltration, the lysozyme enzyme undergoes conformational changes, which can affect its antibacterial activity. Operational conditions are considered to be one of the main parameters responsible for such changes, especially when using the same membrane and molecule. The present study demonstrates that, the same cut-off membrane (commercial data) can result in different properties of the protein after filtration, due to their different pore network. The filtration of lysozyme, regardless of the membrane, produces a decrease in the membrane hydraulic permeability (between 10 and 30%) and an increase in its selectivity in terms of observed rejection rate (30%). For the filtrated lysozyme, it appears that the HPLC retention time increases depending on the membrane used. The antibacterial activity of the filtrated samples is lower than the native protein and decreases with the increase of the applied pressure reaching 55-60% loss for 12 bar which has not been reported in the literature before. The observed results by SEC-HPLC and bacteriological tests, suggest that the conformation of the filtrated molecules are indeed modified. These results highlight the relationship between protein conformation or activity and the imposed shear stress.

Synthesis of FAU-Type Zeolite Membranes with Antimicrobial Activity.

In this study, a layer of a pure and dense phase of FAU-type zeolite was synthesized directly on the surface of α-Al2O3 plane macroporous support. Before hydrothermal synthesis, a step of cleaning of the support by an anionic detergent was performed, a roughness surface is created, allowing the anchoring of the zeolite nuclei and then their growth, favoring in this sense the formation of a homogeneous zeolite layer. The obtained membranes were fully characterized using X-ray diffraction analysis (XRD), nitrogen sorption, scanning electron microscopy (SEM), and mercury porosimetry. After 24 h of thermal treatment at 75 °C, a homogeneous zeolite layer composed of bipyramidal crystals of FAU-type zeolite is obtained with a thickness of about 2.5 µm. No obvious defects or cracks can be observed. It was found that the increase in heating temperature could lead to the appearance of an impurity phase, GIS-type zeolite. Then the ideal zeolite membrane was exchanged with Ag+ or Zn2+ cations to studies their antimicrobial properties. Zeolites membranes exchanged with Ag+ showed an agar-diffusive bactericidal activity against gram negative Escherichia coli (E. coli) bacteria. Zn2+ exchanged zeolite membrane presented a bacteriostatic activity that is less diffusive in agar. As expected, non-exchanged zeolite membrane (in its Na+ form) have no effect on bacterial activity. This process is particularly interesting for the synthesis of a good quality FAU-type zeolite membranes with antimicrobial properties.

Systems for stimuli-controlled release: Materials and applications.

The design and development of delivery controlled systems of molecules of interest has attracted great interest over the last years. pH variation, light irradiation, temperature increasing, variation of the redox potential and the application of a magnetic field are among the most widely used stimuli that can be used to induce the release of an active molecule in a medium. The dominance of pH and photo-controlled release is clearly highlighted by the numerous articles published in these fields as well as all the related applications. In the case of pH-controlled release, two main parameters govern the release: the solubility of the active molecule in the releasing medium and the stability of the carrier materials. In the photo-controlled release, the carrier needs to contain a photosensible functionality; this stimulus can be successfully applied in the medical field when red light, that is able to penetrate the human tissues, is used. A large panel of applications of controlled release can be identified in the pharmaceuticals, agriculture, cosmetics, chemistry and dyes industry fields. More recently, biological, enzymatic, and mechanical (ultrasounds, stretching, shear stress) stimuli have been developed for target applications, in particular for drugs and hormones release. Consequently, many types of materials (polymers, silica, oxides, MOF…) can be used as carrier in relation to their compatibility with the active molecule and the type of releasing medium. This review aims to gives a useful overview on the materials, applications and mechanisms implied in stimuli-controlled release.

Modification of the Selectivity Properties of Tubular Ceramic Membranes after Alkaline Treatment.

This work focuses on the selectivity modification of ceramic membranes after a mild alkaline treatment. Filtration of pure salt-water solutions was carried out with commercial titania membranes before and after the treatment. After treatment, the rejection of NaF significantly decreased, while the rejection of NaCl and NaBr increased. Additionally, NaI and Na2SO4 remained close to zero. Pore size and electrical charge being almost unchanged, only significant modifications in the dielectric effects can explain this modification of selectivity. Therefore, the surface chemistry and the interaction (nature and magnitude) with the solvent and with the species present in the solution appear to be modified by the alkaline treatment. This trend is also illustrated by discussing the electric and the dielectric properties that were numerically identified before and after treatment. The alkaline treatment significantly decreased the apparent dielectric constant of NaCl-water solution in the pore, highlighting the rejection of sodium chloride. Contrariwise, the modification of the surface chemistry increased the apparent dielectric constant of NaF-water solution by promoting fluoride transmission.

Prediction of the mechanical properties of zeolite pellets for aerospace molecular decontamination applications.

Zeolite pellets containing 5 wt % of binder (methylcellulose or sodium metasilicate) were formed with a hydraulic press. This paper describes a mathematical model to predict the mechanical properties (uniaxial and diametric compression) of these pellets for arbitrary dimensions (height and diameter) using a design of experiments (DOE) methodology. A second-degree polynomial equation including interactions was used to approximate the experimental results. This leads to an empirical model for the estimation of the mechanical properties of zeolite pellets with 5 wt % of binder. The model was verified by additional experimental tests including pellets of different dimensions created with different applied pressures. The optimum dimensions were found to be a diameter of 10-23 mm, a height of 1-3.5 mm and an applied pressure higher than 200 MPa. These pellets are promising for technological uses in molecular decontamination for aerospace-based applications.

Concentration polarization phenomenon during the nanofiltration of multi-ionic solutions: influence of the filtrated solution and operating conditions.

One of the major difficulties for the prediction of separation performances in the case of multi-ionic mixtures nanofiltration lies in the description of the concentration polarization phenomenon. Usual models available in literature do not take account of the polarization phenomenon or only describe it cursorily. Very few studies dedicated to the understanding and the specific description of the concentration polarization phenomenon are available in literature and a 2-D multi-ionic model describing the layer heterogeneity along the membrane length has never been proposed yet. The model used in the present work, called Pore and Polarization Transport Model (PPTM), allows an accurate description of the concentration polarization layer occurring during the filtration of multi-ionic solutions by taking account of the radial electromigrative transport in the layer, the turbulence, as well as the axial heterogeneity. In this context, the present paper aims at proposing a numerical investigation of the influence of operating conditions on the behavior of the polarization layer occurring at the membrane vicinity. The input parameters governing the transport through the membrane have been assessed in a previous study in the same experimental conditions so that only the polarization layer is investigated here. The proposed model which was previously validated on experimental observed rejection curves is then used to understand how operating conditions, such as applied pressure, feed flow-rate, or divalent ion proportion, govern the polarization phenomenon. For this purpose, concentration and thickness axial profiles along the membrane length and radial profiles within the polarization layer are investigated for various conditions. Finally, the impact of the type of divalent ion and the number of ions is also studied on various mixtures.