Modification Mechanism of Polyamide Reverse Osmosis Membrane by Persulfate: Roles of Hydroxyl and Sulfate Radicals.

Oxidative modification is a facile method to improve the desalination performance of thin-film composite membranes. In this study, we comparatively investigated the modification mechanisms induced by sulfate radical (SO4• -) and hydroxyl radical (HO•) for polyamide reverse osmosis (RO) membrane. The SO4• -- and HO•-based membrane modifications were manipulated by simply adjusting the pH of the thermal-activated persulfate solution. Although both of them improved the water permeability of the RO membrane under certain conditions, the SO4• --modified membrane notably prevailed over the HO•-modified one due to higher permeability, more consistent salt rejection rates over wide pH and salinity ranges, and better stability when exposed to high doses of chlorine. The differences of the membranes modified by the two radical species probably can be related to their distinct surface properties in terms of morphology, hydrophilicity, surface charge, and chemical composition. Further identification of the transformation products of a model polyamide monomer using high-resolution mass spectrometry demonstrated that SO4• - initiated polymerization reactions and produced hydroquinone/benzoquinone and polyaromatic structures; whereas the amide group of the monomer was degraded by HO•, generating hydroxyl, carboxyl, and nitro groups. The results will enlighten effective ways for practical modification of polyamide RO membranes to improve desalination performances and the development of sustainable oxidation-combined membrane processes.

Membrane Scaling and Wetting in Membrane Distillation: Mitigation Roles Played by Humic Substances.

Membrane scaling and wetting severely hinder practical applications of membrane distillation (MD) for hypersaline water/wastewater treatment. In this regard, the effects of feedwater constituents are still not well understood. Herein, we investigated how humic acid (HA) influenced gypsum-induced membrane scaling and wetting during MD desalination. At low concentrations (5-20 mg L-1), HA notably mitigated membrane scaling and wetting. The morphological characterization of scaled membranes revealed that the antiwetting behavior could be ascribed to the formation of a compact and protective gypsum/HA scale layer, which blocked the flow channel of scaling ions and suppressed the intrusion of scale particles into membrane pores. Based on the comprehensive analysis of the scaling process, the formation of the scale layer was related to the heterogeneous crystallization of gypsum on the membrane surface. Moreover, deprotonated HA interfered with the heterogeneous crystallization process by inhibiting the formation of gypsum nuclei and altering the orientation of crystal growth, thus delaying membrane scaling and altering the morphology of the scale layer. Thermodynamic and kinetic analyses further demonstrated the mitigation mechanism of HA. Furthermore, improved fouling reversibility and antiwetting ability in synthetic seawater treatment endowed by HA were observed. This study provides new insight into the roles played by the organic constituents of water/wastewater during membrane desalination, providing a valuable reference for developing novel strategies to improve the performance of MD.

Utilization of Bidirectional Cation Transport in a Thin Film Composite Membrane: Selective Removal and Reclamation of Ammonium from Synthetic Digested Sludge Centrate via an Osmosis-Distillation Hybrid Membrane Process.

Selective removal and resource recovery of ammonium nitrogen (NH4+-N) from high-strength ammonium waste streams is of practical importance for biological wastewater treatment and environmental protection. In this study, we demonstrate the simultaneous removal and reclamation of ammonium from synthetic digested sludge centrate via a novel osmosis-distillation hybrid membrane (ODHM) process. Using NaHCO3 as the draw solute, ammonium diffuses from the synthetic centrate to the draw solution by utilizing the bidirectional cation transport nature of the thin film composite (TFC) membrane. Then, NH4+ is converted to gaseous NH3 at 60 °C and recovered by a sweeping gas membrane distillation (SGMD) process. Herein, the bidirectional transport of monovalent cations in the osmotic process, selectivity of TFC membranes for different cations, and recovery of the draw solution following the extraction of ammonia through the SGMD process were systematically investigated. The removal of NH4+-N from the synthetic centrate achieved 21.34% during a 6-h continuous operation of the ODHM system, with ammonium fluxes through the TFC and SGMD membranes at 1.39 and 0.57 mol m-2 h-1, respectively. A secondary interfacial polymerization was proposed to further enhance ammonium transport through the TFC membrane. Results reported here highlight the potential of the ODHM process for the selective removal and reclamation of ammonium from ammonium-rich waste streams.

Supramolecular assembly of Polydopamine@Fe nanoparticles with near-infrared light-accelerated cascade catalysis applied for synergistic photothermal-enhanced chemodynamic therapy.

Chemodynamic therapy (CDT) via Fenton-like reaction is greatly attractive owing to its capability to generate highly cytotoxic •OH radicals from tumoral hydrogen peroxide (H2O2). However, the antitumor efficacy of CDT is often challenged by the relatively low radical generation efficiency and the high levels of antioxidative glutathione (GSH) in tumor microenvironment. Herein, an innovative photothermal Fenton-like catalyst, Fe-chelated polydopamine (PDA@Fe) nanoparticle, with excellent GSH-depleting capability is constructed via one-step molecular assembly strategy for dual-modal imaging-guided synergetic photothermal-enhanced chemodynamic therapy. Fe(III) ions in PDA@Fe nanoparticles can consume the GSH overexpressed in tumor microenvironment to avoid the potential •OH consumption, while the as-produced Fe(II) ions subsequently convert tumoral H2O2 into cytotoxic •OH radicals through the Fenton reaction. Notably, PDA@Fe nanoparticles demonstrate excellent near-infrared light absorption that results in superior photothermal conversion ability, which further boosts above-mentioned cascade catalysis to yield more •OH radicals for enhanced CDT. Taken together with T1-weighted magnetic resonance imaging (MRI) contrast enhancement (r1 = 8.13 mM-1 s-1) and strong photoacoustic (PA) imaging signal of PDA@Fe nanoparticles, this design finally realizes the synergistic photothermal-chemodynamic therapy. Overall, this work offers a new promising paradigm to effectively accommodate both imaging and therapy functions in one well-defined framework for personalized precision disease treatment.

Cu-chelated polydopamine nanozymes with laccase-like activity for photothermal catalytic degradation of dyes.

The industrial applications of enzymes are usually hindered by the high production cost, intricate reusability, and low stability in terms of thermal, pH, salt, and storage. Therefore, the de novo design of nanozymes that possess the enzyme mimicking biocatalytic functions sheds new light on this field. Here, we propose a facile one-pot synthesis approach to construct Cu-chelated polydopamine nanozymes (PDA-Cu NPs) that can not only catalyze the chromogenic reaction of 2,4-dichlorophenol (2,4-DP) and 4-aminoantipyrine (4-AP), but also present enhanced photothermal catalytic degradation for typical textile dyes. Compared with natural laccase, the designed mimic has higher affinity to the substrate of 2,4-DP with Km of 0.13 mM. Interestingly, PDA-Cu nanoparticles are stable under extreme conditions (temperature, ionic strength, storage), are reusable for 6 cycles with 97 % activity, and exhibit superior substrate universality. Furthermore, PDA-Cu nanozymes show a remarkable acceleration of the catalytic degradation of dyes, malachite green (MG) and methylene blue (MB), under near-infrared (NIR) laser irradiation. These findings offer a promising paradigm on developing novel nanozymes for biomedicine, catalysis, and environmental engineering.

Tourmaline triggered biofilm transformation: Boosting ultrafiltration efficiency and fouling resistance.

Ultralow pressure filtration system, which integrates the dual functionalities of biofilm degradation and membrane filtration, has gained significant attention in water treatment due to its superior contaminant removal efficiency. However, it is a challenge to mitigate membrane biofouling while maintaining the high activity of biofilm. This study presents a novel ceramic-based ultrafiltration membrane functionalized with tourmaline nanoparticles to address this challenge. The incorporation of tourmaline nanoparticles enables the release of nutrient elements and the generation of an electric field, which enhances the biofilm activity on the membrane surface and simultaneously alleviates intrapore biofouling. The tourmaline-modified ceramic membrane (TCM) demonstrated a significant antifouling effect, with a substantial increase in water flux by 60 %. Additionally, the TCM achieved high removal efficiencies for contaminants (48.78 % in TOC, 22.28 % in UV254, and 24.42 % in TN) after 30 days of continuous operation. The fouling resistance by various constituents in natural water was individually analyzed using model compounds. The TCM with improved electronegativity and hydrophilicity exhibited superior resistance to irreversible fouling through increased electrostatic repulsion and reduced adhesion to foulants. Comprehensive characterizations and analyses, including interfacial interaction energies, redox reaction processes, and biofilm evolutions, demonstrated that the TCM can release nutrient elements to facilitate the development of functional microbial community within the biofilm, and generate reactive oxygen species (ROS) on the membrane surface to the degrade contaminants and mitigate membrane biofouling. The electric field generated by tourmaline nanoparticles can promote electron transfer in the Fe(III)/Fe(II) cycle, ensuring a stable and sustainable generation of ROS and bactericidal negative ions. These synergistic functions enhance contaminant removal and reduce irreversible fouling of the TCM. This study provides fundamental insights into the role of tourmaline-modified surfaces in enhancing membrane filtration performance and fouling resistance, inspiring the development of high-performance, anti-fouling membranes.

[Research on computer-aided technology of surgical guide for dental implant].

The present paper was conducted to a systematic method of surgical guide for dental implant based on computer-aided technology through CT data and dental-cast data. By analyzing the patient's CT data, the implant region was planned using image processing techniques. For the specified implant region, the computer-aided method for the rational allocation of dental implant was addressed in a sense of anatomy. With biomechanical principles as well as aesthetical and functional requirements as preconditions, this method can make full use of bone quantity and quality to produce the optimum implantation axis. The transferring of implant planning to the patient was then realized by registration between CT models and dental-cast models. A case research explained the whole process of the surgical guide. The results validated the correctness and feasibility of this method, which has a great significance to enhance the quality and accuracy of implant surgery.

In vitro and in vivo studies of surface-structured implants for bone formation.

BACKGROUND AND METHODS: Micronanoscale topologies play an important role in implant osteointegration and determine the success of an implant. We investigated the effect of three different implant surface topologies on osteoblast response and bone regeneration. In this study, implants with nanotubes and micropores were used, and implants with flat surfaces were used as the control group. RESULTS: Our in vitro studies showed that the nanostructured topologies improved the proliferation, differentiation, and development of the osteoblastic phenotype. Histological analysis further revealed that the nanotopology increased cell aggregation at the implant-tissue interfaces and enhanced bone-forming ability. Pushout testing indicated that the nanostructured topology greatly increased the bone-implant interfacial strength within 4 weeks of implantation. CONCLUSION: Nanotopography may improve regeneration of bone tissue and shows promise for dental implant applications.