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A durable catalyst composed of Ca-Co bimetallic complex structures on a large-scale substrate was fabricated for efficient activation of peroxymonosulfate (PMS) in organic pollutant degradation. Specifically, amidoxime groups were introduced onto the polymer substrate via radiation-induced graft polymerization (RIGP), followed by selective adsorption of Ca2+ and Co2+ ions. The catalyst demonstrated high effectiveness and stability in degrading 10 mg/L of tetracycline hydrochloride within 8 min by activating PMS under a broad pH range of 3–9. Structural characterization and density functional theory (DFT) calculations confirmed the precise doping of Ca2+, which regulated the energy level and enhanced the dispersion of Co2+. The combination of bulk substrates and fine structural control in catalytic process provided new ideas for the design of similar catalysts., Applied Catalysis B: Environmental, 331, ISSN:1873-3883, ISSN:0926-3373

Developing a practical strategy to fabricate an anti-abrasion and durable superhydrophobic wood surface with ultraviolet (UV) resistance has great practical significance for expanding the application of natural wood. In this study, a robust superhydrophobic layer with a hierarchical micro/nano-roughness structure was modified on the wood surface through in-situ mineralization and polymerization using a simple sol–gel method along with efficient electron beam (EB) curing technology. Hydrophobic agent (polydimethylsiloxane, PDMS), and crosslinking monomer (γ-methacryloxypropyl trimethoxysilane, MAPS) form new covalent bonds between TiO2 particle layer and wood substrate after EB radiation, which endows robust superhydrophobicity and remarkable UV resistance on the wood surface. The as-prepared wood exhibited a water contact angle of approximately 165.7° and obvious repellency to many aqua-phase liquids (cola, strongly acidic, alkaline droplets etc.). Furthermore, the hierarchical micro/nano-protrusion structures remained unchanged and micro/nano particles aggregated tightly on the as-prepared wood surface under harsh external environments (sandpaper abrasion and, ultrasonic treatment), confirming the desirable anti-abrasion and mechanically durable performance of the superhydrophobic surface. After the 18-day UV accelerated weathering test, the TiO2 particle layer conspicuously retained the discoloration and maintained its exceptional repellency toward water. The biomimetic superhydrophobic wood with excellent mechanical durability and UV resistance reveals its potential application in the furniture and architecture fields.

Metal organic frameworks (MOFs) are a distinct family of crystalline porous materials finding extensive applications. Their synthesis often requires elevated temperature and relatively long reaction time. We report here the first case of MOF synthesis activated by high-energy (1.5 MeV) electron beam radiation from a commercially available electron-accelerator. Using ZIF-8 as a representative for demonstration, this type of synthesis can be accomplished under ambient conditions within minutes, leading to energy consumption about two orders of magnitude lower than that of the solvothermal condition. Interestingly, by controlling the absorbed dose in the synthesis, the electron beam not only activates the formation reaction of ZIF-8, but also partially etches the material during the synthesis affording a hierarchical pore architecture and highly crystalline ZnO nanoparticles on the surface of ZIF-8. This gives rise to a new strategy to obtain MOF@metal oxide heterostructures, finding utilities in photocatalytic degradation of organic dyes.

Zeolites are a well-known family of microporous aluminosilicate crystals with a wide range of industrial applications. Their industrial synthetic method under hydrothermal condition requires elevated temperature for activation of polymerization reaction and a long crystallization time, and is therefore quite energy-consuming. Herein, for the first time, we utilize high-energy ionizing irradiation (1.5 MeV electron beam) generated by an industrial electron beam accelerator as a distinct type of energy source to activate the formation reaction of Na-A zeolite. The initial efforts afford an attractive reaction process that can be achieved under ambient conditions and completed within minutes with almost quantitative yield, leading to notable energy-saving of one order of magnitude compared to the hydrothermal reaction. More importantly, electron beam irradiation simultaneously exhibits an etching effect during the formation of zeolite generating a series of crystal-defects and additional pore windows that can be controlled by accumulative irradiation dose. These observations give rise to significantly enhanced surface area and heavy metal removal capabilities in comparison with Na-A zeolite synthesized hydrothermally. Finally, we show that this method can be applied to many other types of zeolites.

The leakages of a large number of organic solvents and oil spills not only cause extensive economic losses, but also destroy the ecological environment. However, there were few studies on the surface engineering of adsorption materials for efficient oil-water separation in complex environments. In this research, through surface engineering, the polymer-based foam exhibited high efficiency oil-water separation performance in different pH environments. Hydrophobic groups were introduced onto the surface of nano-sized SiO

Conventional aromatic compounds tend to exhibit the formation of sandwich-shaped excimers and exciplexes between their excited and ground states at high concentrations or in their aggregated states, causing their fluorescence to weaken or disappear due to the aggregation-caused quenching (ACQ) effect. This limits their applications in concentrated solutions or solid materials. Herein, for the first time, ACQ-based pyrene (Py) units are covalently connected to the surface of polyethylene/polypropylene nonwoven fabric (PE/PP NWF) via electron beam preradiation-induced graft polymerization followed by chemical modification. The matrix can be considered a solid solvent and Py units as a solid solute, such that the amount of Py units can be controlled by varying the reaction time. The obtained fluorescent fabric not only exhibits remarkable fluorescence properties with high fluorescence intensity, high quantum yield (>90%), and excellent fluorescence stability after laundering or in harsh chemical environments, but the fluorescence color and intensity, quantum yield, and lifetime can also be regulated by employing the ACQ effect. Additionally, the as-prepared fluorescent fabric can effectively distinguish common monocyclic aromatic hydrocarbons via a simple fluorescence response test.

A mixed water-organic solvent used for amidoximation increased the production cost of an amidoxime-based polymer sorbent and was not environmentally friendly as well. In this work, the amidoximation of an ultrahigh molecular weight polyethylene fiber co-grafted with acrylonitrile and methacrylic acid was carried out in aqueous solution without the use of an organic solvent. The effects of amidoximation parameters including NH2OH concentration, temperature, time, and various solvents on the uranium adsorption performances in both uranium-spiked brine and simulated seawater were investigated. Results indicated that the optimal amidoximation parameters were 5% (w/v) NH2OH, 80 °C, and 24 h. The uranium adsorption capacities of the sorbents amidoximated in aqueous solution were comparable with those of sorbents amidoximated in the various mixed water-organic solvents. Moreover, in comparison with both acidic (pH ∼3) and alkalic (pH ∼11) aqueous solution, the sorbent amidoximated in neutral (pH ∼7) NH2OH aqueous solution achieved higher uranium adsorption capacities in both uranium-spiked brine (112.4 mg/g) and simulated seawater (7.4 mg/g). Additionally, potassium hydroxide (KOH) treatment was a necessary process and indeed significantly increased the uranium adsorption capacity.

Advanced oxidation processes (AOPs) present one of the most promising strategies to deal with the ever-growing water pollution. However, fabricating improved catalysts with large size (meter level or larger), long-term stability, and adequate activity is still a formidable challenge in practical applications. In this study, cobalt ions are covalently linked on the polypropylene nonwoven fabric (P-PFeCo) via irradiation graft polymerization and used as highly efficient and stable reaction sites to degrade highly toxic and difficult biodegradable organics by activating peroxymonosulfate (PMS). The presence of graft chains not only generates a well-defined monometallic reaction microenvironment, but also promotes electron transfer. The as-prepared catalyst combines these exceptional properties for efficient removal of dyes or antibiotics via activating PMS within 8 min and exhibits remarkable durability over a wide pH range and recyclability after five consecutive runs with trace cobalt leaching. The X-ray absorption fine structure (XAFS) spectroscopy and density functional theory (DFT) calculations reveal that the CoN4(H2O)2 site acts as an active site for activating PMS. A device in a flow mode is also constructed to illustrate the potential applications of P-PFeCo. We consider that the catalytic process along with the large-sized substrate will broaden a new horizon in terms of designing high-performance catalysts for PMS activation in wastewater treatment.

Natural amino acids are non-toxic thermodynamic hydrate inhibitors without negative environmental impact, but it is difficult to accurately select the appropriate amino acid as a quick response to the operational conditions changes in the natural gas pipeline. The objective of this study was to develop mathematical models to predict the hydrate formation temperature (HFT) in presence of amino acids, capture the relationship between amino acid structure properties and their hydrate inhibition strength, and determine the optimal type and concentration to use. The HFT prediction was evaluated using multiple linear regression (MLR) and three machine learning methods including random forest (RF), M5 Rule (M5R) and support vector machine (SVM). After parameter optimization using the trial-and-error method, the coefficient of determination (R2) of the four models were 0.9328, 0.9793, 0.9795 and 0.9980, respectively. The SVM prediction of HFT outperformed other models as the root mean square error (RMSE) was 83%, 76% and 69% lower than that of the MLR, RF and M5R, respectively. Results also demonstrated that the relative importance of the amino acid concentration to the hydrate phase equilibrium was 5-fold higher than that of the intrinsic properties of the amino acid molecular. The SVM model proposed in this study served an easy-to-use tool for reliable prediction of HFT by just providing a new set of input data. This made it possible to accurately determine the minimum concentration of amino acids to be used during the gas pipeline transportation.

A new technique is proposed for the in situ printing of fluorescent fabrics with superior fluorescent properties that have the potential for continuous roll-to-roll production in the industry. Nonconjugated chemical moieties were covalently connected to polyethylene/polypropylene nonwoven fabric (PE/PP NWF) to successfully prepare fluorescent PE/PP NWF, which emits a bright blue light and has a high quantum yield (∼83.35%) that can be attributed to a unique aggregation-induced emission effect. The fluorescent PE/PP NWF exhibits excellent fluorescent stability under high shear forces during accelerated laundering and in harsh chemical environments. The fluorescent PE/PP NWF can also be tailored into diverse shapes and printed in situ with high resolution. The versatility of the method was also demonstrated by fabricating fluorescent materials with different polymer matrices such as Nylon 66 fiber and PE terephthalate membrane.

Solidified natural gas technology shows significant potential for storing safely multi-fold volumes of natural gas in clathrate hydrates, but the main concern is the stochastic and slow process of hydrate nucleation making it unstable and unpredictable in practice. To overcome this limitation, methane hydrate was synthesized in a silicon carbide (SiC) ceramic foam packing trays reactor without stirring. Results suggested that the packing trays should be located near the gas-water interface instead of immersed in the aqueous phase, which decreased the induction time by about 98%. Results also highlighted the synergistic effects between the capillary wicking from the porous packings and the water suction from the initially formed hydrate clusters, which pumped water from the aqueous phase into the packings’ pores to provide an unsaturated porous environment for hydrate nucleation. It demonstrated that these two driving forces might also compete for water which became adverse to hydrate formation.

Immobilization of photocatalysts on substrates is an important factor for water purification in practical applications. In this study, an efficient Ag@AgBr photocatalytic coating was attached onto the surface of cotton fabric via radiation-induced graft polymerization and subsequent chemical reactions, and the resultant product was denoted as Cot-Ag@AgBr. The graft chains acted not only as a source of bromine, but also as an intermediate layer to anchor the Ag@AgBr photocatalytic coating via strong electrostatic interactions. The immobilized Ag@AgBr photocatalytic coating exhibited outstanding photocatalytic properties for organic dye degradation under visible light irradiation. Furthermore, Cot-Ag@AgBr presented high stability and robust durability, which conferred its excellent visible-light-driven photocatalytic activity after five rounds of photodegradation. After 10 min of ultrasonication, the amount of Ag@AgBr precipitate that leached from the Cot-Ag@AgBr was

Crystalline porous materials such as covalent organic frameworks (COFs) are advanced materials to tackle challenges of catalysis and separation in industrial processes. Their synthetic routes often require elevated temperatures, closed systems with high pressure, and long reaction times, hampering their industrial applications. Here we use a traditionally unperceived strategy to assemble highly crystalline COFs by electron beam irradiation with controlled received dosage, contrasting sharply with the previous observation that radiation damages the crystallinity of solids. Such synthesis by electron beam irradiation can be achieved under ambient conditions within minutes, and the process is amendable for large-scale production. The intense and targeted energy input to the reactants leads to new reaction pathways that favor COF formation in nearly quantitative yield. This strategy is applicable not only to known COFs but also to new series of flexible COFs that are difficult to obtain using traditional methods.

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.

Textiles with fire detection will appeal for the interior decoration of houses and play a critical role in public security. Herein, we fabricated a sandwichlike fire alarm fabric (Ag@Fe3O4-MS) base...

A new amidoxime-functionalized ultrahigh molecular weight polyethylene fibrous adsorbent (UHMWPE-g-PAO) was used for the recovery of Au(III) from acid aqueous solution. The maximum experimental absorption capacity of UHMWPE-g-PAO fiber was found to be approximately 220.0 mg·g−1. Au adsorption on UHMWPE-g-PAO was characterized by synchrotron radiation-based microcomputed tomography (SR-μ-CT), transmission electron microscopy (TEM), X-ray absorption near-edge structure spectroscopy (XANES) and synchrotron radiation-based Fourier transform infrared microspectroscopy (SR-FTIR). The SR-μ-CT and TEM results showed the distribution features of gold particles on the fiber. The mechanism of Au(III) recovery from aqueous solutions by UHMWPE-g-PAO was based on the adsorbed Au(III) ions, which were reduced to metallic zero-valent gold (Au(0)) by amino groups (–NH2) in the amidoxime (AO) groups during the adsorption process, as confirmed by high-resolution TEM (HRTEM) and XANES analyses. X-ray diffraction (XRD) results indicated that the incineration ashes contained metallic zero-valent gold. In conclusion, this amidoxime-functionalized fibrous adsorbent is a promising material for recovering gold from aqueous solution.

The thermal stability and surface adhesion of natural gas hydrate are critical for the safety of oil and gas pipelines. The roughness and hydrophobicity of the pipe surface often vary during long-distance transportation, but it remains unclear about how these variances influence the hydrate stability. In this study, twelve molecular models of solid steel pipeline surfaces with random morphology were evaluated and molecular dynamics simulations were performed to gain insights into the kinetics of methane hydrate dissociation, the nucleation and growth of gas bubbles during hydrate decomposition, and the free energy of hydrate adhesion to the solid steel surface. Results demonstrated that the stability of methane hydrate could be decreased by up to 85% by increasing the hydrophobicity of the pipe surface by 52%. The bubble nucleation site of the gas released from hydrate decomposition shifted from bulk water to the solid surface by increasing the surface hydrophobicity (: 3.73–5.74 kJ mol−1), but a highly hydrophobic surface (: 2.73 kJ mol−1) made it hard to form gas bubble on either smooth or rough surface. Moreover, the free energy of hydrate adhesion also depended on the roughness and hydrophobicity of the solid surface, while the largest energy barrier for the adhesion of methane hydrate was found on the hydrophobic surface with high roughness. The findings from this study provided theoretical support for better understanding the methane hydrate evolution principles when the surface properties of the pipe wall changed from naturally occurred events (e.g., metal corrosion) or artificial treatment (e.g. chemical coating).

Gastrointestinal tract cancers have high incidence and mortality in China, but their molecular characteristics have not been fully investigated. We sequenced 432 tumor samples from the colorectum, stomach, pancreas, gallbladder, and biliary tract to investigate cancer-related mutations and detail the landscape of microsatellite instability (MSI), tumor mutation burden (TMB), and chromosomal instability (CIN). We observed the highest TMB in colorectal and gastric cancers and the lowest TMB in gastrointestinal stromal tumors (GISTs). Twenty-four hyper-mutated tumors were identified only in colorectal and gastric cancers, with a significant enrichment of mutations in the polymerase genes (POLE,POLD1, andPOLH) and mismatch repair (MMR) genes. Additionally, CIN preferentially occurred in colorectal and gastric cancers, while pancreatic, gallbladder, and biliary duct cancers had a much lower CIN. High CIN was correlated with a higher prevalence of malfunctions in chromosome segregation and cell cycle genes, including the copy number loss ofWRN,NAT1,NF2, andBUB1B, and the copy number gain ofMYC,ERBB2,EGFR, andCDK6. In addition,TP53mutations were more abundant in high-CIN tumors, whilePIK3CAmutations were more frequent in low-CIN tumors. In colorectal and gastric cancers, tumors with MSI demonstrated much fewer copy number changes than microsatellite stable (MSS) tumors. In colorectal and gastric cancers, the molecular characteristics of tumors revealed the mutational diversity between the different anatomical origins of tumors. This study provides novel insights into the molecular landscape of Chinese gastrointestinal cancers and the genetic differences between tumor locations, which could be useful for future clinical patient stratification and targeted interventions.

Developing a practical strategy to fabricate an anti-abrasion and durable superhydrophobic wood surface with ultraviolet (UV) resistance has great practical significance for expanding the application of natural wood. In this study, a robust superhydrophobic layer with a hierarchical micro/nano-roughness structure was modified on the wood surface through in-situ mineralization and polymerization using a simple sol–gel method along with efficient electron beam (EB) curing technology. Hydrophobic agent (polydimethylsiloxane, PDMS), and crosslinking monomer (γ-methacryloxypropyl trimethoxysilane, MAPS) form new covalent bonds between TiO2 particle layer and wood substrate after EB radiation，which endows robust superhydrophobicity and remarkable UV resistance on the wood surface. The as-prepared wood exhibited a water contact angle (WCA) of approximately 165.7° and obvious repellency to many aqua-phase liquids (cola, strongly acidic, alkaline droplets etc.). Furthermore, the hierarchical micro/nano-protrusion structures remained unchanged and micro/nano particles aggregated tightly on the as-prepared wood surface under harsh external environments (sandpaper abrasion and, ultrasonic treatment), confirming the desirable anti-abrasion and mechanically durable performance of the superhydrophobic surface. After the 18-day UV accelerated weathering test, the TiO2 particle layer conspicuously retained the discoloration and maintained its exceptional repellency toward water. The biomimetic superhydrophobic wood with excellent mechanical durability and UV resistance reveals its potential application in the furniture and architecture fields.