Antioxidant Minerals Modified the Association between Iron and Type 2 Diabetes in a Chinese Population.

Inconsistent findings exist regarding the relationship between heme iron intake and type 2 diabetes (T2D) among Western and Eastern populations. Easterners tend to consume a plant-based diet which is abundant in antioxidant minerals. To examine the hypothesis that antioxidant mineral may modify the relationship between iron and T2D, we performed a case-control study by measuring the serum mineral levels in 2198 Chinese subjects. A total of 2113 T2D patients and 2458 controls were invited; 502 T2D patients and 1696 controls were finally analyzed. In the total population, high serum iron showed a positive association with T2D odds (odds ratio [OR] = 1.27 [1.04, 1.55]); high magnesium (OR = 0.18 [0.14, 0.22]), copper (OR = 0.27 [0.21, 0.33]), zinc (OR = 0.37 [0.30, 0.46]), chromium (OR = 0.61 [0.50, 0.74]), or selenium concentrations (OR = 0.39 [0.31, 0.48]) were inversely associated with T2D odds. In contrast, in individuals with higher magnesium (>2673.2 µg/dL), zinc (>136.7 µg/dL), copper (>132.1 µg/dL), chromium (>14.0 µg/dL), or selenium concentrations (>16.8 µg/dL), serum iron displayed no association with T2D (p > 0.05). Serum copper and magnesium were significant modifiers of the association between iron and T2D in individuals with different physiological status (p < 0.05). Our findings support the idea that consuming a diet rich in antioxidant minerals is an effective approach for preventing T2D.

An easy and unique design strategy for insoluble humic acid/cellulose nanocomposite beads with highly enhanced adsorption performance of low concentration ciprofloxacin in water.

In this work, two plant wastes were reused to fabricate the homogeneous 3D micro-nano porous structured humic acid/cellulose nanocomposite beads (IHA@CB) embedded with insoluble humic acid (IHA) particles. The subtle synthesis method attributed to the homogenous distribution of IHA particles in the cellulose matrix and improved the adsorption performance of IHA@CB for low concentration ciprofloxacin in water. Physical and chemical properties of the beads were characterized by SEM, EDX, XRD, FTIR, and the adsorption process of ciprofloxacin was studied by isotherm, kinetic and dynamic adsorption experiments. The maximum adsorption capacity of IHA@CB on CPX reached 10.87 mg g-1 under 318 K. The dynamic experiments were conducted by adjusting bed height, flow rate, initial concentration and pH values, and the regeneration experiments proved the adsorbent exhibited good repeatability. The adsorption mechanism was revealed that CPX was adsorbed by IHA@CB mainly through cation exchange.

Highly efficient removal of amoxicillin from water by Mg-Al layered double hydroxide/cellulose nanocomposite beads synthesized through in-situ coprecipitation method.

Amoxicillin in the municipal water system needs to be removed due to the toxicity towards creatures. In this work, Mg-Al LDH/cellulose nanocomposite beads (LDH@CB) were synthesized by an in situ coprecipitation procedure and were used as novel adsorbents for amoxicillin removal in the aqueous phase. Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), The specific surface area test (BET), scanning electron microscopy (SEM), ζ potential, X-ray electron energy (XPS) were employed to confirm the success load of LDH onto CB. The large specific surface area (76.46 m2 g-1), high water content (92.05%) and high porosity (94.75%) of LDH@CB made the adsorbent suitable in water treatment. The adsorption process was kinetically fitted with the pseudo second-order kinetic model while isothermally fitted with the Freundlich isotherm model. It was found that the maximum adsorption capacity of LDH@CB qm was 138.3 mg g-1. Meanwhile, the results from XPS and ζ potentials revealed the AMX removal mechanism: Under natural pH conditions, AMX was negatively charged and LDH@CB was positively charged, the contaminant and the adsorbent were linked by electrostatic interaction through OCO⋯M (Mg/Al). These results showed that the adsorbent design method had a wide application prospect in the water purification field.

A simple strategy to design 3-layered Au-TiO2 dual nanoparticles immobilized cellulose membranes with enhanced photocatalytic activity.

Cellulose-based photocatalysts of supported nanoparticles feature high photocatalytic activity but their facile construction and photocatalytic mechanism exploration are highly challenging. Herein, a simple structural design principle and synergistic properties of 3-layered porous cellulose-based membranes are used for catalytic degradation of Rhodamine B in an aqua system. The 3-layered Au-TiO2 cellulose membranes were fabricated through the tape method and the suction filtration process. The composite membranes with strong redox ability, high charge-separation efficiency, and wide absorption range could stimulate the solar-driven plasma evaporation of Au nanoparticles and the photocatalytic function of TiO2 nanoparticles simultaneously. As characterized by Scanning Electron Microscopy, well-defined Au nanoparticles with an average size of 18.24 ±â€¯3.17 nm were uniformly distributed on the TiO2-CM surface. Compared with TiO2-CM, TiO2-Au-CM showed better catalytic degradation of organic dye. This work demonstrated that a simple strategy design of Au-TiO2-CM could efficiently enhance the photocatalytic activity for the degradation of dyes in water.

Facile synthesis and low concentration tylosin adsorption performance of chitosan/cellulose nanocomposite microspheres.

Antibiotic pollution in tap water, surface water, and effluent needs to be controlled in China. Adsorption is an economical and eco-friendly way to solve the antibiotic contamination problem, such as tylosin. In this study, the chitosan/cellulose nanocomposite adsorbents entrapped with activated carbon are prepared by a sol-gel phase inversion method. Structures and properties of the adsorbents are characterized by SEM, EDXS, BET, XRD, FTIR XPS and Zeta potentials. The adsorption behavior of CCM-AC on tylosin is determined by batch and fixed-bed adsorption experiments, while their adsorption mechanism is also studied. The maximum adsorption capacity is 59.26 mg g-1, while the adsorption behavior is in accordance with the Langmuir equation and pseudo-second-order kinetics. These results confirm that the tylosin adsorption process is affected by chemical and physical interactions, and the adsorbent can be captured by tylosin with H-bond, electrostatic and π-π electron-donor-acceptor interaction. Adsorption experiments are significantly affected by pH.