Ion exchange materials show great advantages in water purification, food industry, pharmaceutical industry, etc. However, the ion exchange capacities of ion exchange materials, especially for anion-exchange materials, at present are still relatively low. Hydrogels own abundant functional groups and show high hydrophilicity, and thus are recognized as high-potential ion exchange materials, but may deform and even crush in use due to their low mechanical strength and unavoidable swelling behavior. In this study, inspired by the root-soil structure, novel poly(methacryloxyethyltrimethyl ammonium chloride) composite hydrogel microspheres with ultrahigh ion exchange capacity (more than 3.8 meuqiv/g), low swelling ratio (less than 1.5 g/g under pH = 7), and ultrahigh mechanical strength (more than 28.1 MPa) were prepared. The microspheres showed efficient adsorption for anionic dyes (1491 mg/g for methyl orange, 1693 mg/g for Congo red, and 204.7 mg/g for amaranth, respectively) and great adsorption for bilirubin (131.6 mg/g). Taken together, the hydrogel microspheres were qualified as stable and high-efficiency ion exchange materials. More importantly, the root-soil structure opens up avenues for enhancing the dimensional stability of functional hydrogels.

The presence of dyes in wastewater effluents made from the textile industry is a major environmental problem due to their complex structure and poor biodegradability. In this study, a cationic lignin polymer was synthesized via the free radical polymerization of lignin with [2-(methacryloyloxy) ethyl] trimethyl ammonium chloride (METAC) and used to remove anionic azo-dyes (reactive black 5, RB5, and reactive orange 16, RO16) from simulated wastewater. The effects of pH, salt, and concentration of dyes, as well as the charge density and molecular weight of lignin-METAC polymer on dye removal were examined. Results demonstrated that lignin-METAC was an effective flocculant for the removal of dye via charge neutralization and bridging mechanisms. The dye removal efficiency of lignin-METAC polymer was independent of pH. The dosage of the lignin polymer required for reaching the maximum removal had a linear relationship with the dye concentration. The presence of inorganic salts including NaCl, NaNO₃, and Na₂SO₄ had a marginal effect on the dye removal. Under the optimized conditions, greater than 98% of RB5 and 94% of RO16 were removed at lignin-METAC concentrations of 120 mg/L and 105 mg/L in the dye solutions, respectively.

The presence of carcinogens in food is a major food safety concern. A nanocomposite-based electrochemical DNA biosensor was constructed for potential carcinogen detection in food samples by immobilizing amine terminated single stranded DNA onto silica nanospheres deposited onto a screen-printed electrode modified using gold nanoparticles. The effect of three different DNA sequences: 15-base guanine, 24-base guanine and 24-base adenine-thymine rich DNA on carcinogen (formaldehyde and acrylamide) detection was evaluated. The competitive binding of the DNA with the carcinogen and electroactive indicator, Methylene blue (MB) was measured using differential pulse voltammetry. Optimization studies were conducted for MB concentration and accumulation time, DNA concentration, buffer concentration, pH and ionic strength. Overall, the 24-base guanine rich DNA yielded the best results with a detection limit of 0.0001 ppm, linear range between 0.0001 ppm and 0.1 ppm and reproducibility below 5% R.S.D. Finally, the results obtained using the biosensor were validated using Ames test.

Total suspended particle (TSP) samples were collected during a cruise campaign over the western South China Sea (SCS) from August to September 2014. Ten water-soluble ions (WSI), organic carbon (OC), elemental carbon (EC) and stable carbon isotope ratios of total carbon (δ13CTC) were measured. The average concentrations of total WSI, OC and EC were 7.91 ± 3.44 μg/m3, 2.04 ± 1.25 μg/m3 and 0.30 ± 0.22 μg/m3, respectively. Among the investigated WSI, sulfate (SO42-), sodium (Na+) and chloride (Cl-) were the most abundant species, accounting for 39.2%, 24.5% and 14.3% of the total mass of the WSI, respectively. Significantly positive correlations of OC and EC with non-sea-salt potassium (nss-K+), a tracer for biomass burning, suggest that biomass burning is the major source of carbonaceous aerosols. The values of δ13CTC ranged from -26.6‰ to -24.4‰ with an average of -25.3 ± 0.7‰. Based on the literature data of δ13CTC, back-trajectory analysis and satellite fire spots, we propose that C3 plant burning in Southeast Asia significantly contributes to carbonaceous aerosols over the western SCS. This is also supported by a good correlation between δ13CTC and the mass ratios of nss-K+/TC. Furthermore, high Cl- depletion (73 ± 23%) was observed in the aerosols over the western SCS. Given the neutralization of SO42- by ammonium (NH4+), excess nss-SO42- and oxalate (C2O42-) made major contributions to Cl- depletion in the samples strongly influenced by biomass burning. This study provides useful information to better understand the influence of biomass burning on atmospheric aerosols over the SCS.

The authors describe colorimetric test strips by using electrospun nanofiber membranes (NFMs) carrying gold/silver core/shell nanoparticles (Au/Ag NPs). The Au/Ag NPs were immobilized on aminated porous polyacrylonitrile NFMs to obtain test strips with a tortuous porous structure and a large surface area (38.6 m2 g-1). The color of the resultant NFMs, measured at a wavelength of 420 nm, is red-shifted when exposed to copper ions (Cu2+) with a color change from yellow to pink to colorless. The effect is due to leaching Au/Ag NPs from the NFMs in the presence of ammonium chloride, thiosulfate and Cu2+ upon which soluble thiosulfate complexes of Ag+, Au3+ and Cu2+ are formed. The effect can be readily seen with bare eyes. Under optimized conditions, this method has a low limit of detection (50 nM at S/N = 3), a fast assay time (3 min), good specificity, and excellent reversibility. The colorimetric test strip was successfully applied to the analysis of Cu2+ in drinking water sample. Graphical abstract Schematic of the preparation of test strips for Cu2+ by immobilizing Au/Ag core-shell nanoparticles on aminated polyacrylonitrile nanofibers.

Here we report a facile method to construct reversible visible-light-responsive switching from antibacterial to bioadhesion by host-guest self-assembly of β-cyclodextrin (β-CD) and azobenzene functionalized polycation/polyanion. The visible-light-responsible azobenzene functionalized polycation, poly{6-[(2,6-dimethoxyphenyl)azo-4-(2',6'-dimethoxy)phenoxy]propyl dimethylaminoethyl methacrylate-random-poly(2-(N,N-dimethylaminoethyl) methacrylate) (Azo-PDMAEMA), was synthesized via quaternization reaction between 2,6,2',6'-tetramethoxy-4-(3-bromopropoxy)azobenzene (AzoOMeBr) and poly(2-(N,N-dimethylaminoethyl) methacrylate) (PDMAEMA), and the polyanion, poly{6-[(2,6-dimethoxyphenyl)azo-4-(2',6'-dimethoxy) phenoxy]hexyl acrylate-random-acrylic acid} (Azo-PAA), was synthesized via esterification reaction between 2,6,2',6'-tetramethoxy-4-(6-hydroxyhexyloxy) azobenzene (AzoOMeOH) and poly(acryloyl chloride) (PAC) and subsequent hydrolysis reactions. The switch surface could be achieved via the alternate host-guest assembly of Azo-PDMAEMA and Azo-PAA onto a β-CD-terminated substratum (Sub-CD) through visible light irradiation. The positively charged Azo-PDMAEMA with quaternary ammonium groups exhibited antimicrobial properties and few bacteria were adhered on the surface, while the negatively charged Azo-PAA with carboxyl acid groups exhibited excellent bioadhesive properties and a large number of bacteria were adhered. Interestingly, the switch between antibacterial and bioadhesive could be realized upon visible light irradiation via alternate assembly of Azo-PDMAEMA and Azo-PAA. The proposed approach to manufacturing visible-light-responsive surface with reversible and alterable biofunctionality switching between antibacterial and bioadhesive is simple and efficient, which is promising for preparation of multifunctional polymeric surfaces to encounter multifarious demands for the biomedical and biotechnological applications.

This study compared physiological and productive parameters in 3/4 Holstein × 1/4 Gir dairy cows receiving a prepartum concentrate containing ammonium chloride to reduce urine pH near 7.0 (CON; n = 17), or a commercial anionic supplement to reduce urine pH near 6.0 (SUPP; n = 17). Nonlactating, multiparous, pregnant cows were assigned to receive SUPP or CON beginning 21 d before expected date of calving. Cows were maintained in a single drylot pen with ad libitum access to corn silage, and individually received their prepartum concentrate once daily (0800 h) before calving. Cows from both treatments completely consumed their concentrate allocation within 30 min after feeding. Cow body weight and body condition score were recorded once weekly, urine pH measured every 3 d, and blood samples collected on d -21, -14, -9, -6, and -3 relative to expected calving date. After calving (d 0), cows were moved to an adjacent drylot pen with ad libitum access to water and a total mixed ration, and were milked twice daily (0600 and 1700 h). Cow body weight and body condition score were recorded once weekly and individual milk production was recorded daily until 30 d in milk (DIM). Blood samples were collected before each milking during the first 5 DIM, as well as at 6, 9, 16, 23, and 30 DIM before the morning milking. Based on actual calving dates, cows received SUPP or CON for (mean ± standard error) 19.2 ± 1.2 and 19.0 ± 0.9 d before calving, respectively. Urine pH was less in SUPP versus CON cows during the last 15 d of gestation (6.12 vs. 7.15, respectively). Milk yield during the first 5 DIM and throughout the experimental period was greater in SUPP versus CON cows (by 20 and 14%, respectively), whereas serum Ca concentrations did not differ between treatments during the first 5 DIM. Serum concentrations of fatty acids were greater in SUPP versus CON cows 3 d before and at calving (by 52 and 22%, respectively), whereas SUPP cows had lower serum glucose and cortisol concentration at calving (by 23 and 27%, respectively). Hence, the SUPP treatment decreased prepartum urine pH near 6.0 in Holstein × Gir dairy cows without depressing concentrate intake compared with CON, although total dry matter intake was not evaluated to fully investigate feed intake responses. Moreover, the SUPP treatment transiently affected serum glucose, fatty acids, and cortisol concentrations near the time of calving, and resulted in greater milk yield during the initial 30 DIM compared with CON.

Using a solvent formed of alkali and urea, chitosan was successfully dissolved in a new solvent via the freezing⁻thawing process. Subsequently, quaternized chitosan (QC) was synthesized using 3-chloro-2-hydroxypropyl trimethyl ammonium chloride (CHPTAC) as the cationic reagent under different incubation times and temperatures in a homogeneous system. QCs cannot be synthesized at temperatures above 60 °C, as gel formation will occur. The structure and properties of the prepared QC were characterized and quaternary groups were comfirmed to be successfully incorporated onto chitosan backbones. The degree of substitution (DS) ranged from 16.5% to 46.8% and the yields ranged from 32.6% to 89.7%, which can be adjusted by changing the molar ratio of the chitosan unit to CHPTAC and the reaction time. QCs inhibits the growth of Alicyclobacillus acidoterrestris effectively. Thus, this work offers a simple and green method of functionalizing chitosan and producing quaternized chitosan with an antibacterial effect for potential applications in the food industry.