Influence of the hydrogen reduction time and temperature on the morphology evolution and hematite/magnetite conversion of spindle-type hematite nanoparticles

We report on the transformation via hydrogen reduction of spindle-type hematite nanoparticles into hematite/magnetite hybrid iron oxide particles. The transformation process consists of the reduction of nanoparticles powder in an autoclave using hydrogen gas at a fixed pressure of 11 bars. Both temperature and time of reduction are varied between 300 °C to 360 °C and 0 to 45 h. X-Ray powder diffraction data on the obtained powder and corresponding Rietveld refinement allow the amount of reduced hematite to be determined as a function of these two parameters. Kinetics parameters are measured and an estimation of the activation energy is obtained through linearization of the Arrhenius equation. While reduction is dramatically accelerated at higher temperature, the morphology of the nanoparticles only remain qualitatively unchanged at 300 °C as seen from transmission electron microscopy images. The mechanisms underlying morphology changes are still under study and seem to be closely related to reactor pressure.     

Alternative approaches to trip distribution modelling: A retrospective review and suggestions for combining different approaches

Abstract.  Various alternative approaches are available in the literature for modelling trip distribution. The objective of this paper is to provide a review of this literature with the view of summarising the general nature of the current state of practise and what is now available for practical modelling work. Both aggregate and disaggregate destination choice models are considered, a classification of them will be proposed and suggestions for further research will be given as well. One outcome of this review is that significant contributions are emerging from mixed models (e.g., gravity-opportunity, random utility, intervening opportunities models, etc). In particular, the review will highlight the benefit of integrating different approaches like the introduction of intervening opportunities factors within random utility models.     

Geotextile filtration opening size under tension and confinement

Nonwoven geotextiles have been used as filters in geotechnical and geoenvironmental works for half a century. They are easy to install and can be specified to meet the requirements for proper filter performance. There are situations where a geotextile filter may be subjected to tensile loads, which may alter relevant filter properties, such as its filtration opening size. Examples of such situations are silty fence applications, geotextile separators, geotextile tubes and geotextiles under embankments on soft soils. This paper investigates the effects of tensile strains on geotextile pore dimensions. A special equipment and testing technique allowed tests to be carried out on geotextile specimens subjected to tension and confinement. The results obtained showed that the variation in filtration opening size depends on the type of strain state the geotextile is subjected, under which the geotextile pore diameter may remain rather constant or increase significantly. However, confinement reduces the geotextile filtration opening size independent on the strain mobilised. An upper bound for the filtration opening size of strained nonwoven geotextiles is introduced and was satisfactory for the geotextile products tested.     

Large-scale load capacity tests on a geosynthetic encased column

Stone columns have been used to minimize the settlement of embankments on soft soils but their use in very soft soils can become challenging, partly because of the low confinement provided by the surrounding soil. Geosynthetic encased columns (GECs) have been successfully used to enhance to reduce settlements of embankments on soft soils. This paper describes an investigation on the performance of encased columns constructed on a very soft soil using different types of encasement (three woven geotextiles with different values of tensile stiffness) and different column fill materials (sand, gravel and recycled construction and demolition waste, RCDW). The results of load capacity tests conducted on large-scale models constructed to simulate the different types of GECs indicate that the displacement method adopted during column installation can lead to an enhanced shear strength in the smear zone that develops within the very soft soil. In addition, breakage of the column fill material was found to affect the load-settlement response of gravel and RCDW columns. Furthermore, the excess pore water pressure generated in the surrounding soil during installation, was found to remain limited to radial distances smaller than three times the GEC diameter.     

Biomimetic Concealing of PLGA Microspheres in a 3D Scaffold to Prevent Macrophage Uptake

Scaffolds functionalized with delivery systems for the release of growth factors is a robust strategy to enhance tissue regeneration. However, after implantation, macrophages infiltrate the scaffold, eventually initiating the degradation and clearance of the delivery systems. Herein, it is hypothesized that fully embedding the poly(d,l ‐lactide‐co‐glycolide acid) microspheres (MS) in a highly structured collagen‐based scaffold (concealing) can prevent their detection, preserving the integrity of the payload. Confocal laser microscopy reveals that non‐embedded MS are easily internalized; when concealed, J774 and bone marrow‐derived macrophages (BMDM) cannot detect them. This is further demonstrated by flow cytometry, as a tenfold decrease is found in the number of MS engulfed by the cells, suggesting that collagen can cloak the MS. This correlates with the amount of nitric oxide and tumor necrosis factor‐α produced by J774 and BMDM in response to the concealed MS, comparable to that found for non‐functionalized collagen scaffolds. Finally, the release kinetics of a reporter protein is preserved in the presence of macrophages, only when MS are concealed. The data provide detailed strategies for fabricating three dimensional (3D) biomimetic scaffolds able to conceal delivery systems and preserve the therapeutic molecules for release.     

Use of a toasted durum whole meal in the production of a traditional Italian pasta: chemical, mechanical, sensory and image analyses

The characterisation of traditional Italian pasta obtained by mixing amounts of toasted whole meal with re-milled semolina and other ingredients was obtained by means of physico-chemical, rheological, mechanical, sensory and image analyses. The toasted meal showed higher ash, fibre and protein contents than re-milled semolina. The replacement of percentages of re-milled semolina with the toasted meal and soft flour increased tenacity and decreased extensibility and strength, making the dough less suitable for pasta-making. The P / L values were indices of high starch damage. The replacement of part of re-milled semolina and water with toasted whole wheat meal, soft flour and eggs increased the optimal cooking time and the amount of water absorbed during cooking but made the other cooking parameters worse. The image analysis provided evidence of the changes induced by the use of toasted wholemeal, soft flour and eggs in the microscopic structure of pasta protein and starch.     

Microfluidic devices modulate tumor cell line susceptibility to NK cell recognition

This study aims to adoptively reduce the major histocompatibility complex class I (MHC-I) molecule surface expression of cancer cells by exposure to microfluid shear stress and a monoclonal antibody. A microfluidic system is developed and tumor cells are injected at different flow rates. The bottom surface of the microfluidic system is biofunctionalized with antibodies (W6/32) specific for the MHC-I molecules with a simple method based on microfluidic protocols. The antibodies promote binding between the bottom surface and the MHC-I molecules on the tumor cell membrane. The cells are injected at an optimized flow rate, then roll on the bottom surface and are subjected to shear stress. The stress is localized and enhanced on the part of the membrane where MHC-I proteins are expressed, since they stick to the antibodies of the system. The localized stress allows a stripping effect and consequent reduction of the MHC-I expression. It is shown that it is possible to specifically treat and recover eukaryotic cells without damaging the biological samples. MHC-I molecule expression on treated and control cell surfaces is measured on tumor and healthy cells. After the cell rolling treatment a clear reduction of MHC-I levels on the tumor cell membrane is observed, whereas no changes are observed on healthy cells (monocytes). The MHC-I reduction is investigated and the possibility that the developed system could induce a loss of these molecules from the tumor cell surface is addressed. The percentage of living tumor cells (viability) that remain after the treatment is measured. The changes induced by the microfluidic system are analyzed by fluorescence-activated cell sorting and confocal microscopy. Cytotoxicity tests show a relevant increased susceptibility of natural killer (NK) cells on microchip-treated tumor cells.     

Mesoporous silicon particles as a multistage delivery system for imaging and therapeutic applications

Many nanosized particulate systems are being developed as intravascular carriers to increase the levels of therapeutic agents delivered to targets, with the fewest side effects. The surface of these carriers is often functionalized with biological recognition molecules for specific, targeted delivery. However, there are a series of biological barriers in the body that prevent these carriers from localizing at their targets at sufficiently high therapeutic concentrations. Here we show a multistage delivery system that can carry, release over time and deliver two types of nanoparticles into primary endothelial cells. The multistage delivery system is based on biodegradable and biocompatible mesoporous silicon particles that have well-controlled shapes, sizes and pores. The use of this system is envisioned to open new avenues for avoiding biological barriers and delivering more than one therapeutic agent to the target at a time, in a time-controlled fashion.