Novel Biocompatible Polysaccharide-Based Eutectogels with Tunable Rheological, Thermal, and Mechanical Properties: The Role of Water.

The natural deep eutectic solvent (NADES) is an excellent solvent for insoluble natural products and medicines. Eutectogels formed by gelation of NADESs are interesting materials that deserve attention. In this study, xanthan gum was used as a gelator to gel choline chloride-xylitol with different water contents in virtue of the excellent solubility of choline chloride-xylitol (1:1) to quercetin. We observed that water was critical to the formation of eutectogels. An MTT assay indicated that our eutectogel had excellent biocompatibility as its corresponding hydrogel. According to rheological tests, xanthan gum-based eutectogels had better viscoelastic properties, higher thermal stability, and more defined shear thinning behavior than its corresponding hydrogel. Texture profile analysis showed that eutectogels with less water content had higher hardness and adhesiveness. Meanwhile, Differential scanning calorimeter (DSC) results suggested that the various rheological and texture properties of eutectogels could be attributed to changes in the water state, which was influenced by the hydrogen bonding network of NADES. This biocompatible eutectogel with tunable properties was expected to find applications in novel drug delivery vehicles, which are widely used in the fields of medicine and food.

Ambivalent effects of dissolved organic matter on silver nanoparticles/silver ions transformation: A review.

The numerous applications of silver nanoparticles (AgNPs) lead to their spread in aquatic systems and the release of silver ions (Ag+), which brings potential risks to environment and human health. Owing to the different toxicity, the mutual transformations between AgNPs and Ag+ has been a hot topic of research. Dissolved organic matter (DOM) is ubiquitous on the earth and almost participates in all the reactions in the nature. The previous studies have reported the roles of DOM played in the transformation between AgNPs and Ag+. However, different experiment conditions commonly caused contradictory results, leading to the difficulty to predict the fate of AgNPs in specific reactions. Here we summarized mechanisms of DOM-mediated AgNPs oxidation and Ag+ reduction, and analyzed the effects of environmental parameters. Moreover, the knowledge gaps, challenges, and new opportunities for research in this field are discussed. This review will promote the understanding of the fate and risk assessments of AgNPs in natural water systems.

Computer vision-assisted smartphone microscope imaging digital immunosensor based on click chemistry-mediated microsphere counting technology for the detection of aflatoxin B1 in peanuts.

Aflatoxin B1 is a carcinogenic contaminant in food or feed, and it poses a serious health risk to humans. Herein, a computer vision-assisted smartphone microscope imaging digital (SMID) immunosensor based on the click chemistry-mediated microsphere counting technology was designed for the detection of aflatoxin B1 in peanuts. In this SMID immunosensor, the modified polystyrene (PS) microspheres were used as the signal probes and were recorded by a smartphone microscopic imaging system after immunoreaction and click chemistry reaction. The number of PS probes is adjusted by aflatoxin B1. The customized computer vision procedure was used to efficiently identify and count the obtained PS probes. This SMID immunosensor enables sensitive detection of aflatoxin B1 with a linear range from 0.001 ng/mL to 500 ng/mL, providing a simple, sensitive, and portable tool for food safety supervision.

Influence of nitrate/nitrite on the degradation and transformation of triclosan in the UV based disinfection.

This study investigated the influence of nitrate/nitrite on the degradation and transformation pathway of triclosan (TCS) in UV, UV/peracetic acid (PAA) and UV/HClO processes. The results indicated that the function of nitrate/nitrite significantly depended on the UV source and wavelength, especially nitrate. Generally, the presence of nitrate decreased the direct photo-degradation of TCS in the UV based disinfection. In the LED-UV and LED-UV/HClO processes, the presence of nitrate improved the radical oxidation, and transformation pathway of TCS was varied accordingly. However, nitrate more played a role of photo-competitor in the UV/PAA process, and the reactive nitrogen species (RNS) was difficult to participant in the degradation of TCS due to low redox potential. Compared to nitrate, the presence of nitrite decreased the degradation of TCS in three different UV based disinfection processes. Under UV irradiation, nitrite primarily acted as an irradiation competitor and radical scavenger. Thus, the indirect photo-degradation of TCS was reduced. Noticeably, nitrate/nitrite were the improtant precersors of nitrogenous products in the UV base disinfection. Many new nitrogenous products were identified. But RNS preferentially reacted with the intermediates by -NO2 addition compared to directly reacted with TCS.

Effect of different DOM components on arsenate complexation in natural water.

Dissolved organic matter (DOM) and dissolved ions are two integral parameters to affect the environmental fate of As in different ways. Numerous studies chose surrogate of DOM, humic substances (HSs), to investigate the As complexation behavior. However, microbial secretion (protein and polysaccharide) was also considered for a great proportion in surface aquatic system, and its effect was still not fully understood. The present research distinguished the As complexation behavior with different DOM components (HSs, protein, polysaccharide and synthetic organic matter) in natural and simulated water samples. The results indicated that different DOM components exhibited various binding capacities for As. HSs showed the strongest affinity for As, followed by long-chain compounds (polysaccharide and synthetic organic matter) and proteins. In water source, HSs were probably the primary parameter for As complexation. In eutrophic water system, however, polysaccharide maybe the main DOM component to bind As. Cationic bridge function was prone to occur in the presence of HSs, but not observed in the presence of protein. PO43- competed for binding sites with As, consequently decreasing the As complexation with all the DOM components. The research implied that a comprehensive and meticulous analyses of DOM fractions and coexist ions are the prerequisite to understanding the behavior of As (or other pollutants) in different natural aquatic systems.

Influence of dissolved organic matter components on arsenate adsorption/desorption by TiO2.

The influences of different dissolved organic matter (DOM) components and ionic matters on As(V) adsorption/desorption behavior on the TiO2 surface were investigated. The results demonstrated that the characteristics and involving order of DOM significantly affected the As(V) adsorption/desorption behavior. The presence of DOM decreased the As(V) adsorption quantity. Fulvic acid (FA) exhibited the most negative effect, and followed by the order of alginate ≈ BSA > SDBS. The precomplexation DOM prevented more As(V) adsorption. While, the presence of DOM caused more As(V) release when the surrounding changed and FA exhibited the strongest effect. The results indicated that the site competition and electrostatic repulsion were the major mechanisms to resist As(V) adsorption. The presence of Fe3+ and Ca2+ increased As(V) adsorption by bridge effect, while PO43- and CO32- decreased As(V) adsorption owing to the competition.

Degradation mechanism of lignocellulose in dairy cattle manure with the addition of calcium oxide and superphosphate.

Cellulose and lignin belongs to refractory organic matters in the traditional composting. In this research, the degradation of lignocellulose in dairy cattle manure was investigated through adding calcium oxide (CaO) and superphosphate (SSP). In the presence of CaO and SSP, the degradation rate of cellulose and lignin were improved by 25.0% and 8.33%, respectively. The results indicated that the pH value in system would be slightly higher with the addition of CaO and SSP. Besides, the pH value of all cow manure piles were about 8.4 after composting rotten, which could be well neutralized by the gradually acidified soil in the southwest of China with the full effect of fertilizer released. In addition, the abundance of Bacillales, Actinomycetes, and Thermoactinomycetaceae in the experimental groups (AR) was slightly better than that in the control groups (CK) during composting, which led to a conclusion that an elaborate physical-chemical-multivariate aerobic microorganism evolution model of cellulose degradation products (PCMC) was deduced and the physical-chemical-multivariate aerobic microorganism model of lignin cycle degradation (PCML) was developed.

Aggregation behavior of TiO2 nanoparticles in municipal effluent: Influence of ionic strengthen and organic compounds.

The influence of ionic strengthen and dissolved organic matter (DOM) on the aggregation of TiO2 nanoparticles (NPs) in municipal effluent was investigated. The results demonstrated that DOM promoted the mobility of NPs in aquatic system by synergism between static repulsion and steric effect, while electrolytes were opposite by charge-neutralization. The physical-chemical characteristics of DOM played the major role on the mobility of NPs. Bovine serum albumin (BSA) showed the strongest enhancement on the mobility of TiO2 NPs. High adsorption of BSA introduced vast negative charges on the TiO2 NPs' surface, leading to static repulsion and neutralizing positive charges of electrolytes in surrounding as well. By contrast, another protein α-amylase retarded the aggregation rate of TiO2 NPs through steric repulsion of the long-chain construction. Humic substances (Fulvic acid and alginate) also reflected the combination of static repulsion and steric effect. However, in the high electrolytes concentration (especially Ca2+), the long-chain aliphatic compounds were prone to form calcium bridge which increased the hydrodynamic diameter of TiO2 aggregates consequently. Sodium dodecylbenzene sulfonate (SDBS) showed low adsorption capacity, while the unabsorbed SDBS retarded the aggregates caused by the changes of pH and electrolytes. These data indicated that decreasing of DOC concentration in aqueous system was important to reduce the mobility and potential risk of NPs in aqueous system.