Hydration products of FBC wastes as SO2 sorbents: comparison between ettringite and calcium hydroxide

Fluidized bed combustion (FBC) enables the in situ capture of SO₂, but generates large amounts of wastes whose composition and physico-chemical properties make both landfilling and reuse in traditional fields of application (e.g., cement and concrete industries) problematic. Reactivation by water hydration of the desulphurizing ability of these residues is considered a viable mean for their recycling: besides Ca(OH)₂, this process can generate other hydration products, such as ettringite. This paper is devoted to a comparison between the behaviour of Ca(OH)₂ and ettringite as SO₂ sorbents. To this end, synthetic preparations (in the particle size range 0.4–0.6 mm) of the two materials were dehydrated and then sulphated in a lab-scale fluidized bed reactor. Sulphation tests were carried out at 850 °C by fluidizing the bed with an SO₂–N₂–O₂ mixture (1800 ppm SO₂) at 0.8 m/s. Calcium conversion degree and fines elutriation rate were evaluated as a function of sulphation time. The propensity of the sorbents to undergo fragmentation was also estimated by particle sizing of in-bed exhausted sorbent particles, with the aid of laser granulometry. Mercury intrusion porosimetry of samples was directed to the assessment of the influence of sorbent dehydration and subsequent sulphation on pore size distribution and porosimetric texture. X-ray diffraction and differential thermal analysis on the synthetic sorbents complemented the characterization. Results showed that dehydration/thermal decomposition brought about a significant increase of the overall porosity for both sorbents, more extensive than it is commonly observed with calcined commercial limestones. Upon sulphation, the two sorbents showed satisfactory degrees of calcium conversion, larger than those usually observed with limestones. Sulphation resulted into a decrease of particle voidage (that of the Ca(OH)₂-based sorbent was negligible after the process). Ettringite was more prone to attrition/fragmentation than calcium hydroxide. Results are discussed with a focus on differences between calcium hydroxide and ettringite and on key-parameters affecting the performance of the two materials as sorbents.     

High methoxyl pectin–methyl cellulose films with antioxidant activity at a functional food interface

The effect of using increasing proportions of methylcellulose (MC) for the development of glycerol plasticized films based on high methoxyl pectin (HMP) (30:70, 50:50 and 70:30 w/w HMP:MC) and carrying l-(+)-ascorbic acid (AA) was studied with the purpose of achieving higher stability of AA and localized antioxidant activity at food interfaces. MC and 30:70 HMP:MC systems could not be casted. The shelf-life of the other AA-active films was assessed by storage at 25 °C, constant relative humidity (RH: 33.3%, 57.7% and 75.2%) and vacuum conditions. The rate constant for AA hydrolysis increased with the RH and, hence, with water mobility. Browning and AA degradation rates were directly related. When stored at 75.2% RH, both decreased as MC proportion increased. Compared to HMP film, the highest proportion of MC (50:50 HMP:MC) showed the highest AA stabilization under vacuum and greater performance under air atmosphere. They also developed localized antioxidant activity preserving the tocopherol content of walnut oil.     

Real and perceived feet orientation under fatiguing and non-fatiguing conditions in an immersive virtual reality environment

Virtual Reality - Lower limbs position sense is a complex yet poorly understood mechanism, influenced by many factors. Hence, we investigated the position sense of lower limbs through feet...     

Additive Manufacturing of Porous Biominerals

Nature fabricates hard functional materials from soft organic scaffolds that are mineralized. To enable an energy-efficient locomotion of these creatures while maintaining their structural stability, nature often renders parts of these minerals porous. Unfortunately, methods to produce synthetic minerals with a similar degree of control over their multi length scale porous structure remain elusive. This level of control, however, would be required to design lightweight yet robust biominerals. Here, a room temperature process is presented that combines a localized mineralization with emulsion-based 3D printing to form cm sized biominerals possessing pores whose diameters range from the 100 s of nm up to the mm length scale. The samples encompass up to 80 wt% of CaCO₃ and display a specific compressive strength that is significantly higher than that of previously reported 3D printed porous biominerals and close to those of trabecular bones. The universality of this approach by forming different types of bioactive minerals, including calcite, aragonite, and brushite is demonstrated. The ability to 3D print these materials under benign conditions renders this energy-efficient process well-suited to construct cm-sized lightweight yet load-bearing structures that might find applications, for example, in the design of the next generation of flying or motile objects.