Application of Natural Antibacterial Plants in the Extraction of Uranium from Seawater.

Marine biofouling directly affects the performance and efficiency of uranium (U(VI)) extraction from seawater. Compared to traditional chemical methods, natural plant extracts are generally biodegradable and nontoxic, making them an environmentally friendly alternative to synthetic chemicals in solving the marine biofouling problem. The effectiveness of natural antibacterial plants (i.e., pine needle, peppermint, Acorus gramineus Soland, Cacumen platycladi, and wormwood) in solving the marine biofouling problem was evaluated in this work. Experimental results showed that natural antibacterial plants could kill Vibrio alginolyticus in solution and effectively solve the marine biofouling problem of U(VI) extraction. To improve the adsorption capacity of natural plants for U(VI) in seawater, poly(vinylphosphonic acid) (PVPA) was modified on natural antibacterial plant surfaces by irradiation grafting technology. PVPA and natural antibacterial plants work as active sites and base materials for the U(VI) extraction material, respectively. The recovery performance of PVPA/pine needle for U(VI) was preliminarily studied. Results show that the adsorption of U(VI) on PVPA/pine needle follows pseudo-second-order and Langmuir models, and the maximum adsorption capacity is 111 mg/g at 298 K and pH 8.2.

Elimination of uranium pollution from coastal nuclear power plant by marine microorganisms: Capability and mechanism.

Uranium is one of the sensitive radionuclides in the wastewater of nuclear powers. Due to the fact that nuclear powers are mainly located in coastal areas, the elimination of uranium (U(VI)) pollution from coastal nuclear power is ultimately rely on marine microorganisms. The fixing of U(VI) on V. alginolyticus surface or converting it into sediments is an effective elimination strategy for U(VI) pollution. In this work, typical marine microorganism V. alginolyticus was used to evaluate the elimination of U(VI) pollution by marine microorganisms. Effects of solution conditions (such as pH, temperature, and bacterium concentrations) on the physicochemical properties and elimination capabilities of V. alginolyticus were studied in detail. FT-IR, XPS and XRD results reveal that COOH, NH2, OH and PO4 on V. alginolyticus were main functional groups for U(VI) elimination and formed (UO2)3(PO4)2·H2O. The elimination of U(VI) by V. alginolyticus includes two stages of adsorption and biomineralization. The theoretical maximum adsorption capacity (Cs,max) of V. alginolyticus for U(VI) can reach up to 133 mg/g at pH 5 and 298 K, and the process reached equilibrium in 3 h. Results show that V. alginolyticus play important role in the elimination of U(VI) pollution in seawater.

Fabrication of new conductive surface-metallized UHMWPE fabric with improved thermal resistance.

A new UHMWPE-based conductive fabric was successfully prepared by radiation-induced graft polymerization and subsequent post-modification, followed by electroless deposition. The chemical structure and composition of modified UHMWPE fabrics were investigated in detail by ATR-FTIR, 29Si NMR, and XPS to confirm grafting and post-modification. After electroless deposition, the morphology, thermal stability, and crystal structure of original and modified fabrics were characterized by SEM, TG, DSC and XRD. Cu-deposited UHMWPE fabric exhibited much better thermal resistance than that of UHMWPE and Cu@UHMWPE-g-PAAc. In order to improve the oxidation resistance of copper-deposited fabric, nickel was processed on copper-coated UHMWPE fabric to protect the copper layer. An electromagnetic shielding effect test showed the nickel-copper coated UHMWPE fabric could shield 94.5% of the electromagnetic wave in the frequency range of 8-12 GHz. This work provides an approach for addressing the issue of poor thermal resistance of metal-coated polymeric materials due to the inherent low melting point of the organic support.

Enhanced removal of I- on hierarchically structured layered double hydroxides by in suit growth of Cu/Cu2O.

To further improve the removal ability of layered double hydroxide (LDH) for iodide (I-) anions from wastewater, we prepared hierarchically porous Cu5Mg10Al5-LDH and used as a matrix for in suit growth of Cu/Cu2O on its surface, forming Cu/Cu2O-LDH, which was characterized and applied as an adsorbent. Results displayed high I- saturation uptake capability (137.8 mg/g) of Cu/Cu2O-LDH compared with Cu5Mg10Al5-LDH (26.4 mg/g) even thermal activated LDH (76.1 mg/g). Thermodynamic analysis showed that the reaction between I- anions and Cu/Cu2O-LDH is a spontaneous and exothermic. Uptake kinetics analysis exhibited that adsorption equilibrium can be reached after 265 min. Additionally, the adsorbent showed satisfactory selectivity in the presence of competitive anions (e.g., SO42-), and could achieve good adsorption performance in a wide pH range of 3-8. A cooperative adsorption mechanism was proposed on the basis of the following two aspects: (1) ion exchange between iodide and interlayer anions; (2) the adsorption performance of Cu, Cu(II) and Cu2O for I-. Meanwhile, the difference between the adsorption mechanism of Cu/Cu2O-LDH, Cu5Mg10Al5-LDH and Cu5Mg10Al5-CLDH adsorbents was also elaborated and verified.

In-situ formation of durable akaganeite (ß-FeOOH) nanorods on sulfonate-modified poly(ethylene terephthalate) fabric for dual-functional wastewater treatment.

Industrial oily wastewater with dye-pollution is a critical environmental issue for water purification. However, the fabrication of effective and stable materials for oil-water separation and simultaneous degradation of organic contaminants remains a critical challenge. Herein, we report a new process for in-situ formation of akaganeite (ß-FeOOH) nanorods layer on the surface of poly(ethylene terephthalate) (PET) fabric via radiation-induced graft polymerization of glycidyl methacrylate, which is then sulfonated and mineralized. The resultant product is labeled as ß-FeOOH@PET, which exhibits dual purification by demonstrating an effective oil-water separation and organic dyes photodegradation under the illumination of visible light. It provides stable performance even after 1000 wash cycles. The sulfonated layer acts as not only an electronic transport layer to prevent electron-hole recombination, but also as an anchored interface for immobilizing ß-FeOOH nanorods on the sulfonated layer via strong covalent bonds. Overall, the superhydrophilicity and underwater superoleophobicity of ß-FeOOH@PET fabric, along with its robustness with a flexible organic substrate and its dual purification function, provide a new insight toward oily wastewater remediation and water purification in large-scale applications.

Fabrication of hydrophilic and antibacterial poly(vinylidene fluoride) based separation membranes by a novel strategy combining radiation grafting of poly(acrylic acid) (PAA) and electroless nickel plating.

This study proposed a novel strategy to improve performance of inherently hydrophobic poly(vinylidene fluoride) (PVDF) membrane. The proposed strategy combined radiation grafting of poly(acrylic acid) (PAA) and electroless nickel plating. After a 5 min plating by using this modification strategy, the water contact angle of the modified membrane decreased from 75.5° to 47.1°, and water content ratio increased from 61.4% to 109.9%. The modified PVDF-g-PAA-Ag@Ni membrane presented 100% flux recovery and reduced fouling propensity when filtrating 0.1 g/L sodium alginate (SA) solution. Moreover, involvement of silver in this strategy provided evident antibacterial activity of the modified membranes. The ease and high efficiency of this strategy point towards the potential widespread applications of this strategy and the modified membranes.

Nanometer mixed-valence silver oxide enhancing adsorption of ZIF-8 for removal of iodide in solution.

Nano mixed-valence silver oxide (Ag2O-Ag2O3) modified the zeolitic imidazolate framework-8 (ZIF-8) composite (Ag2O-Ag2O3@ZIF-8) was firstly prepared via a simple and efficient method, characterized and applied for iodide ion (I-) uptake from simulated radioactive wastewater. The results showed that Ag2O-Ag2O3 nanoparticles doped and uniformly dispersed on the surface of ZIF-8 matrix. The adsorption capacity of the as-synthesized adsorbents increased with the increasing Ag doped amount, and the maximum adsorption capacity for 20%-Ag2O-Ag2O3@ZIF-8 was 232.12 mg/g. The calculated thermodynamic parameters indicating that the adsorption was a spontaneous and exothermic. It was worth mentioning that each Ag-based adsorbent exhibited high uptake rate of I-, and all the adsorption tests were equilibrated for a few minutes. This could be ascribed to its large specific surface area and the absolutely dominant position of chemical adsorption for as-prepared samples. Furthermore, the adsorption was barely affected by pH and competitive anions (e.g. Cl-, SO42-, CO32-), even in simulated salt lake water. Additionally, a mechanism explaining the excellent properties for adsorbents could be epitomized into three aspects, namely, the uptake performance of Ag2O for I-, the strong oxidization of Ag2O3 for I-, and the adsorption of AgI for I2.

Significant Improvement in Thermal and UV Resistances of UHMWPE Fabric through in Situ Formation of Polysiloxane-TiO2 Hybrid Layers.

Anatase nanocrystalline titanium dioxide coatings were produced on ultrahigh molecular weight polyethylene (UHMWPE) fabric by radiation-induced graft polymerization of γ-methacryloxypropyl trimethoxysilane (MAPS) and subsequent cohydrolysis of the graft chains (PMAPS) with tetrabutyl titanate, followed by boiling water treatment for 180 min. The resulting material was coded as UHMWPE-g-PMAPS/TiO2 and characterized by attenuated total reflection infrared spectrometry, differential scanning calorimetry, X-ray diffraction, thermal gravimetry, and ultraviolet absorption spectroscopy, among others. The predominant form of TiO2 in the thin film was anatase. The coating layer was composed of two sublayers: an inner part consisting of an organic-inorganic hybrid layer to prevent photocatalytic degradation of the matrix by TiO2 film, and an outer part consisting of anatase nanocrystalline TiO2 capable of UV absorption. This UHMWPE-g-PMAPS/TiO2 composite exhibited much better thermal resistance than conventional UHMWPE fabric, as reflected by the higher melting point, decreased maximum degradation rate, and higher char yield at 700 °C. Compared with UHMWPE fabric, UHMWPE-g-PMAPS/TiO2 exhibited significantly enhanced UV absorption and excellent duration of UV illumination. Specifically, the UV absorption intensity was 2.4-fold higher than that of UHMWPE fabric; the retention of the break strength of UHMWPE-g-PMAPS/TiO2 reached 92.3% after UV irradiation. This work provides an approach for addressing the issue of self-degradation of TiO2-coated polymeric materials due to the inherent photoactivity of TiO2.

Preparation and characterization of superhydrophobic organic-inorganic hybrid cotton fabrics via γ-radiation-induced graft polymerization.

A new kind of non-fluorine-based organic-inorganic hybrid superhydrophobic cotton fabric was successfully prepared by simultaneous radiation-induced graft polymerization of γ-methacryloxypropyl trimethoxy silane (MAPS) and subsequent end-capping modification with hexamethyldisilazane (HMDS). The chemical structure and surface topography of the pristine and modified cotton fabrics were investigated in detail by ATR-FTIR, XPS, (29)Si NMR, SEM and TGA to confirm that the graft reaction and end-capping modification had taken place. The above results demonstrated that the grafting polymerization and following end-capping reaction were completed, and a grafting layer was immobilized onto the surface of the cotton fabric. Surface wettability measurement and oil-water separation showed that the modified cotton surface not only exhibited the superhydrophobicity with a water contact angle of 165°, but also afforded a high efficiency of oil-water separation (96%). In particular, this modified cotton fabric retains superhydrophobicity even after 30 laundering cycles or 400 cycles of abrasion.

Folate-polyethylene glycol conjugated carboxymethyl chitosan for tumor-targeted delivery of 5-fluorouracil.

Targeted drug delivery has been evolving at an increasing rate due to its potential to reduce the minimum effective dose of a drug and its accompanying side effects. It has shown improved therapeutic efficacy at equivalent plasma concentrations; however, the development of effective targeted delivery systems has remained a major task. In this study, a drug carrier was designed and synthesized by conjugation of folate acid (FA) to carboxymethyl chitosan (CMCS) through a polyethylene glycol (PEG) spacer. The resulting conjugates were confirmed by 1H nuclear magnetic resonance and infrared spectroscopy. The cytotoxicity of CMCS and CMCS­5­fluorouracil (5­FU) was determined by a crystal violet stain assay. The potential of CMCS­PEG­FA for use in the targeted delivery of 5­FU was investigated using 3­(4,5­dimethylthiazol­2­yl)­2,5­diphenyltetrazolium bromide analysis in two cell lines, HeLa and A549, which contain different numbers of folate receptors on their surfaces. The MTT results revealed that in HeLa cells, the cytotoxicity of (CMCS­5­FU)­PEG­FU cells is greater compared with CMCS­5­FU, suggesting that folate receptor­mediated endocytosis may affect the cellular uptake efficiency of 5­FU­loaded CMCS­PEG­FA. The CMCS­PEG­FA conjugates presented in this study show promise as carriers for chemotherapeutic agents due to their solubility at physiological pH, efficiency in carrying chemotherapeutic agents, low cytotoxicity and targeting ability.