Intelligent pH- and ammonia-sensitive indicator films using neutral red immobilized onto cellulose nanofibrils.

In this study, colorimetric indicator films (CIFs) were developed by integrating neutral red covalently immobilized onto TEMPO-oxidized cellulose nanofibrils (NR@TOCNFs) and poly(acrylic acid) (PAA) inside a poly(vinyl alcohol) (PVA) matrix. The successful covalent immobilization of NR onto the TOCNFs was confirmed using attenuated total reflection-Fourier transform infrared, X-ray photoelectron spectroscopy, and thermogravimetric analyses. The CIFs had a visible color change from red to yellow as the pH changed from 2.0 to 10.0. The colorimetric response of CIFs improved as the NR@TOCNF content increased, while it decreased as the PAA level increased. The critical pH ranges for the color change of CIFs were 6-7, 7-8, and 8-9 for 3 %, 5 %, and 7 % PAA, respectively, at 0.3 % NR@TOCNF. The best ammonia sensitivity was found in the indicator films containing 3 % PAA and 0.3 % NR@TOCNF. These results showed that the CIFs could be applied for freshness detection in food packaging.

Preparation and characterization of air nanofilters based on cellulose nanofibers.

One of the most important environmental issues in the world today is the problem of air pollution, which includes particulate matter (PM) and greenhouse gases (mainly CO2). The production of efficient sustainable filters to overcome this concern as well as to provide an alternative to synthetic petroleum-based filters remains a demanding challenge. The purpose of this research was to first produce novel cellulose nanofibers (CNF) based nanofilter from a combination of CNF and chitosan (CS) and then evaluate its applicability for air purification. A number of structural and chemical properties as well as CO2 and PM adsorption efficiency of the modified CNF, were determined using advanced characterization techniques. After pretests, we determined the optimum loading for the CS was 1 wt%, and upon producing the samples, the CNF loadings (1, 1.5, and 2 wt%) were chosen as one variable. For particle absorption, the PM sizes (0.1, 0.3, 0.5, and 2.5 µm) were kept as other variables. Based on SEM results, we concluded the higher the concentration of CNF the higher the specific surface area and the lower the porosity and the diameter of the pores, which was confirmed by the BET test. Furthermore, the results showed that increasing the concentration of modified CNFs increases the adsorption rate of CO2 and PM and that the highest adsorption of CO2 and PM belonged to the 2% modified CNF.

Bioactive glass 45S5 powders: effect of synthesis route and resultant surface chemistry and crystallinity on protein adsorption from human plasma.

Despite its medical applications, the mechanisms responsible for the osseointegration of bioactive glass (45S5) have yet to be fully understood. Evidence suggests that the strongest predictor for osseointegration of bioactive glasses, and ceramics, with bone tissue as the formation of an apatitic calcium phosphate layer atop the implanted material, with osteoblasts being the main mediator for new bone formation. Most have tried to understand the formation of this apatitic calcium phosphate layer, and other bioresponses between the host and bioactive glass 45S5 using Simulated Body Fluid; a solution containing ion concentrations similar to that found in human plasma without the presence of proteins. However, it is likely that cell attachment is probably largely mediated via the adsorbed protein layer. Plasma protein adsorption at the tissue bioactive glass interface has been largely overlooked. Herein, we compare crystalline and amorphous bioactive glass 45S5, in both melt-derived as well as sol-gel forms. Thus, allowing for a detailed understanding of both the role of crystallinity and powder morphology on surface ions, and plasma protein adsorption. It was found that sol-gel 45S5 powders, regardless of crystallinity, adsorbed 3-5 times as much protein as the crystalline melt-derived counterpart, as well as a greater variety of plasma proteins. The devitrification of melt-cast 45S5 resulted in only small differences in the amount and variety of the adsorbed proteome. Surface properties, and not material crystallinity, play a role in directing protein adsorption phenomena for bioactive glasses given the differences found between crystalline melt-cast 45S5 and sol-gel derived 45S5.