For the first time, alginate polymer has been applied to prevent dyes from leaching out of colorimetric oxygen indicator films, which enable people to notice the presence of oxygen in the package in an economic and simple manner. The dye-based oxygen indicator film suffers from dye leaching upon contact with water. In this work, UV-activated visual oxygen indicator films were fabricated using thionine, glycerol, P25 TiO2, and zein as a redox dye, a sacrificial electron donor, UV-absorbing semiconducting photocatalyst, and an encapsulation polymer, respectively. When this zein-coated film was immersed in water for 24h, the dye leakage was as high as 80.80±0.45%. However, introduction of alginate (1.25%) as the coating polymer considerably diminished the dye leaching to only 5.80±0.06%. This is because the ion-binding ability of alginate could prevent the cation dye from leaching into water. This novel water-resistant UV-activated oxygen indicator was also successfully photo-bleached and regained colour fast in the presence of oxygen.

Mechanical mixtures of macromolecules and simple solutes were investigated with respect to their water adsorption capabilities. The additivity principle was applied to predict sorption isotherms of mixtures on the basis of the sorption behaviour of pure components. Mechanical mixtures of macromolecules and mixtures of biopolymers and simple solutes yielded isotherms which were superimposable with those predicted at the low water activity range. In the multilayer water absorption range, predicted isotherms in most cases overestimated the water contents of mixtures in comparison with experimental values. The reasons for the observed differences between experimental and predicted values are discussed. These may include the ordering of the water in contact with macromolecule surfaces, swelling, conformational changes, polymer-polymer interactions, multiple hydrogen bonds, binding of ions crosslinking, competition for water and plasticization of amorphous regions. The rates of these changes are limited and long time-scale experiments may be needed to observe equilibrium sorption isotherms of mechanical multicomponent mixtures. It is suggested that lack of the additivity of sorption processes should be rather a rule, not an exception in the case of multicomponent mixtures.

Periphyton is ubiquitous in Florida Everglades and has a profound effect on mercury (Hg) cycling. Enhanced methylmercury (MeHg) production in periphyton has been well documented, but the re-distribution of MeHg from periphyton remains unknown. In this study, periphyton, sediments, surface water, periphyton overlying water, and periphyton porewater were collected from Everglades for analyzing the distribution of MeHg and total Hg (THg). Results showed that there were no significant differences in THg and MeHg in different types of periphyton, but they all displayed higher MeHg levels than sediments. MeHg distribution coefficients (logkd) in periphyton were lower than in sediments, suggesting that periphyton MeHg could be more labile entering aquatic cycling and bioaccumulation. In water, the more the distance of water samples taken from periphyton, the lower the MeHg and dissolved organic carbon concentrations were detected. In extracellular polymeric substances of periphyton, MeHg in colloidal fractions was significantly higher than that in capsular fractions. It was estimated that approximately 10% (or 1.35 kg) of periphyton MeHg were passed on to mosquitofish entering the food web during wet season, contributing 73% of total Hg stocked in mosquitofish. These results revealed the importance of periphyton on water MeHg distribution and MeHg bioaccumulation in Everglades.

In this work we demonstrate that the synergistic combination of organic molecules extracted from food waste can empower different types of carboxylated gold nanoparticles (Au NPs) in removal of Cr(VI) species from both milliQ and real water solutions. In particular, chitosan extracted from shrimp’s shell and dissolved in an acidic active medium based on a 1:3 M mixture of ascorbic and citric acid allows citrate-capped Au NPs to improve their abatment efficiency from 18.4 to > 99% in milliQ and 80.6% in drinking water. When citrates are exchanged with 3-mercaptopropionic or 11-mercaptoundecanoic acids, the efficiency reaches 100% in both milliQ and drinking water. 11-mercaptoundecanoic acid is found to be the best capping agent in terms of efficiency and stability. Crossing of cyclic voltammetry and UV–Vis data enabled to define the main role of each individual component in abatment of Cr(VI). This study further advances research on the rational design of hybrid nanoparticle/polymer systems for environmental remediation, inspired by criteria of circular economy and environmental sustainability.

This study was carried out to evaluate the effects of power ultrasound (US) on the molecular weight and rheological properties of a food polysaccharide, konjac glucomannan (KGM). Upon the exposure of KGM solution (1% w/v in water) to US at a relatively high power intensity (50 W/cm2), the apparent viscosity decreased rapidly from about 50 Pa s to a negligible level within 10–20 min. The intrinsic viscosity ([η]) of KGM solution decreased gradually during the US exposure with a time course closely fitted to the first-order polymer degradation kinetics (random chain scission). The US treatment also caused a significant reduction of particle size (Zavg) of KGM aggregates and changes in the rheological properties including the decrease of storage modulus (G′) and loss modulus (G″), and the increase in phase angle (tan δ = G″/G′). Nevertheless, no change in primary structure was detected by Fourier transformation infrared (FT-IR) analysis. The results suggested that high intensity US was an effective means for KGM degradation without significant structural destruction.

The inert nature of most commercial polymers and nanomaterials results in limitations of applications in various industrial fields. This can be solved by surface modifications to improve physicochemical and biological properties, such as adhesion, printability, wetting and biocompatibility. Polymer functionalization allows to graft specific moieties and conjugate molecules that improve material performances. In the last decades, several approaches have been designed in the industry and academia to graft functional groups on surfaces. Here, we review surface decoration of polymers and nanomaterials, with focus on major industrial applications in the medical field, textile industry, water treatment and food packaging. We discuss the advantages and challenges of polymer functionalization. More knowledge is needed on the biology behind cell–polymer interactions, nanosafety and manufacturing at the industrial scale.

The synthesis of new chitin derivatives through ultrasound-assisted treatment of the chitin with 1-azido-3-chloropropan-2-ol under Green Chemistry conditions is described. This is the first example of ultrasound-assisted polymer analogues transformation of chitin unaccompanied by noticeable backbone degradation or deacetylation. The obtained water-soluble azido chitin derivatives are characterized by high antibacterial activity, which is comparable with that of commercial antibiotics ampicillin and gentamicin. At the same time, they were demonstrated almost identical in vitro toxicity as unmodified chitin and chitosan. The antibacterial activity of the obtained polymers is mainly provided by azido moiety in their macromolecules. The conjugation of azido moiety to chitin backbone strongly diminishes the toxicity of the azido pharmacophore, but preserves its antibacterial properties. The most potent chitin derivative was used for the film coating of Ricotta cheese samples. This food coating proved to be efficient for the prolongation of shelf life of Ricotta cheese.

We have previously shown that diarrheagenic Escherichia coli (DEC) and non-DEC are prevalent in food sources and irrigation water in South Africa. Recent data suggest that an increased relative abundance of faecal Enterobacteriaceae is associated with poorer health outcomes among children in developing countries. Thus, exposure to non-DEC from environmental sources may incur adverse effects, although the mechanisms underlying these effects remain obscure. To further elucidate this phenomenon, we assayed non-DEC strains from environmental sources in South Africa for phenotypes that may be associated with intestinal dysfunction (ID). DEC strains were also used. The strains had previously been isolated from Producer Distributor Bulk Milk (PDBM), irrigated lettuce, street vendor coleslaw and irrigation water.In-vitro assays identified; biofilm formation (n = 38), extracellular polymeric substance (EPS) formation (n = 38), cytotoxic activity (n = 10), disruption of tight junctions and induction of Interleukin 8 (IL-8) on polarized T-84 cells (n = 20). The number of strains tested for each assay differed, depending on prior molecular and phenotypic characterization that signalled potential pathogenicity in-vitro. Subsequently, all strains having data points for all analyses were used to compute Principal Component Analysis (PCA) plot curves to infer potential associations amongst test strains and a standard DEC pathogenic strain (042).Biofilm formation on glass coverslips after strains were grown in nutrient-rich media (LB and DMEM-F12 + 0.5% D-Mannose) at 37 °C varied based on pathotype (DEC and non-DEC) and source of isolation (food, irrigation water, clinical) suggesting that pathotype and source isolation influence persistence within a defined environmental niche. Additionally, DEC isolated from irrigated lettuce had a significantly higher (p ≤ 0.05) propensity for biofilm formation in both media compared to all strains including DEC standard controls. This suggested the propensity for irrigated lettuce as a potential source of persistent pathogenic strains. Furthermore, all strains were able to form EPS suggesting the ability to form mature biofilms under conditions relevant for food processing (20–25 °C). Of the (60%, 6 out of 10) strains that showed cytotoxic activity, most (83%, 5 out of 6 strains) were non-DEC isolated from food sources many of which are consumed with minimal processing.Mean percentage reduction in initial TEER (a measure of intestinal disruption), did not significantly differ (p = 0.05) in all test strains from that observed in the standard DEC. Additionally, IL-8 induction from strains isolated from PDBM (139 pg/mL), irrigation water (231.93 pg/mL) and irrigated lettuce (152.98 pg/mL) was significantly higher (p ≤ 0.05) than in the commensal strain aafa. PCA categorized strains based on sources of isolation showed potential for use in source tracking especially when comparing many strains from various environmental sources. We show that non-DEC strains along the food chain possess characteristics that may lead to ID. Further investigations using a larger collection of strains may provide a clearer link to these reported observations that could be associated with the high diarrheal disease burden within the country, especially among infants.

Microemulsions based on five-component mixtures for food applications and improved oil solubilization have been studied. The compositions included water, oil phase [such as R(+)-limonene and medium-chain triglycerides (MCT)], short-chain alcohols (such as ethanol), polyols (propylene glycol and glycerol), and several surfactants and their corresponding mixtures (nonionic, such as ethoxylated sorbitan esters, polyglycerol esters, sugar ester, and anionic, such as phosphatidylcholine). The phase behavior of these systems is discussed with respect to the influence of polyols and short-chain alcohols on the degree of solubilization of oils in the aqueous phase. The alcohol and polyols modify the interfacial spontaneous curvature and the flexibility of the surfactant film, enhancing the oil solubilization capacity of the microemulsions. The solubilization of R(+)-limonene was dramatically improved in the presence of the alcohol and polyols, whereas the improvement of solubilization for triglycerides containing MCT was less pronounced. In some systems high oil solubilization was achieved, and some of them can be easily diluted to infinity both with the aqueous phase and with the oil phase. Viscosity measurements along selected dilution lines [characterized by a single continuous microemulsion region starting from a pseudo binary solution (surfactant/oil phase) to the microemulsion (water/polyol corner)] indicate that at a certain composition the system inverts from a W/O to an O/W microemulsion.