Microvesicle-Embedded Solid-liquid Composite Coating for the Tribological Behavior Regulation and Long-Acting Lubrication.

Friction interfaces in liquid-embedded composite lubrication coatings commonly comprise a combination of discontinuous fluid films and rough solid contact surfaces, which together ensure easy shearing and a prolonged wear life. However, achieving high efficacy in mixed lubrication poses a challenge due to the conflicting nature of enhanced migration freedom for the liquid lubricant and increased mechanical strength of the solid matrix. Recent efforts have focused on incorporating reinforcing fillers to develop multicomponent, multiphase composites that can address this paradox. Here, we describe a modified attapulgite (APT) with strong biphasic wettability via the oil decompressive osmosis treatment on APT nanocontainers grafted with long nonpolar alkyl chains. This modified APT enables control over the size, distribution, and mobility of lubricant droplets by constructing a Pickering emulsion and toughens the solid-phase matrix through dispersion strengthening. Additionally, the introduction of APT induces the formation of a solid tribofilm during friction, which possesses a higher oil adsorption capacity, as verified through first-principles calculations based on density functional theory (DFT). Consequently, the fluid films can be replenished by the fracture of nanocontainers and adsorption from the bulk phase; further comprehensive and effective regulation of the friction interface leads to low friction and wear.

Mechanochemical preparation of low cost kaolinite-based BiVO4hybrid pigments with high near infrared reflectance.

For accelerate construction of the energy and resource-saving and environmental-friendly society, cleaner preparation of low-cost and high-performance colorful near-infrared reflective inorganic pigments with the decorative function is indispensable to reduce the hazards of urban heat island and simultaneously beautify the appearance of the buildings. Due to the non-toxicity, good chemical stability and narrow band gap, BiVO4has been becoming a promising environment-friendly yellow inorganic pigments among the conventional heavy metals-containing inorganic pigments. In this study, the low-cost and brilliant kaolinite-based BiVO4hybrid pigments were fabricated by cleaner mechanochemical method based on cheap and abundant kaolinite using crystal water of the hydrated metal salts as trace solvent, which could effectively promote the interaction of the involved components at the molecular level during grinding and then decreased the mass transfer resistance for the formation of monoclinic scheelite BiVO4in the following calcination. The obtained hybrid pigments at the optimal preparation conditions exhibited brilliant color properties (D65-10°,L*= 83.45 ± 0.08,a*= 4.17 ± 0.08,b*= 88.59 ± 0.17), high near-infrared reflectance of 86.22%, infrared solar reflectance of 88.14% and high emissivity of 0.9369 in the waveband of 8-13µm. Furthermore, the hybrid pigments could be used for coloring epoxy resin with high emissivity of 0.8782 in 8-13µm. Therefore, the brilliant and low-cost kaolinite-based bismuth yellow hybrid pigments have the enormous potential to be served as colorful functional nanofillers for cooling roofing materials.

Fabrication porous adsorbents templated from aqueous foams using astragalus membranaceus and attapulgite as stabilizer for efficient removal of cationic dyes.

The water-based foam stabilized by the natural surfactant applied in the fabrication of porous materials has attracted extensive attention, as the advantages of cleanness, convenience and low cost. Particularly, the development of a green preparation method has became the main research focus and frontier. In this work, a green liquid foam with high stability was prepared by synergistic stabilization of natural plant astragalus membranaceus (AMS) and attapulgite (APT), and then a novel porous material with sufficient hierarchical pore structure was templated from the foam via a simple free radical polymerization of acrylamide (AM). The characterization results revealed that the amphiphilic molecules from AMS adsorbed onto the water-air interface and formed a protective shell to prevent the bubble breakup, and APT gathered in the plateau border and formed a three-dimensional network structure, which greatly slowed down the drainage rate. The porous material polyacrylamide/astragalus membranaceus/attapulgite (PAM/AMS/APT) showed the excellent adsorption performance for cationic dyes of Methyl Violet (MV) and Methylene Blue (MB) in water, and the maximum adsorption capacity could reach to 709.13 and 703.30 mg/g, respectively. Furthermore, the polymer material enabled to regenerate and cycle via a convenient calcination process, and the adsorption capacity was still higher than 200 mg/g after five cycles. In short, this research provided a new idea for the green preparation of porous materials and the treatment of water pollution.

Scale-up disaggregation of palygorskite crystal bundles via ultrasonic process for using as potential drilling fluid.

High-efficient disaggregation of palygorskite (PAL) crystal aggregates into individual nanorods is the key to exploiting its nanometer properties, which remains a challenge at present. The sonochemical cavitation effects have been successfully employed for the intensification of physical and chemical processing applications, but it still lacks the relevant study on the scale-up disaggregation of PAL crystal bundles. Here, the energy-efficient, scale-up ultrasonic process was developed to disaggregate PAL aggregates in batches, and the effects of ultrasonic treatment time, temperature, and power on physicochemical features of PAL were systematically investigated. The results showed that the single dispersed PAL nanorods could be continuously produced by sonicating 15 wt% of PAL suspension at 20 kHz, 2000 W and 30 °C for 5 min retaining the original nanorod length and layered-chain structure. It also greatly improved the dispersion of nanorod crystal, specific surface area and suspension stability of PAL. The ultrasonically disaggregated PAL has a higher pulping rate in water (14.96 m3/t) and saturated NaCl system (14.45 m3/t), which is significantly better than that of natural PAL in water (14.72 m3/t) and saturated NaCl solution (12.37 m3/t). It suggests that the disaggregated PAL exhibits excellent potential and adaptability as a viscosity enhancer for drilling fluid. Therefore, this work provides a feasible and efficient ultrasonic process for large-scale industrialized disaggregation of PAL crystal bundles, laying a foundation for the high-value utilization of natural PAL as one-dimensional nanomaterials.

Recovering metal ions from oxalic acid leaching palygorskite-rich clay wastewater to fabricate layered mixed metal oxide/carbon composites for high-efficient removing Congo red.

This study developed a sustainable way to transform metallic residues in wastewater and spent adsorbents that adsorbed organic pollutants into novel high-efficiency adsorbents to treat water pollution again. The metal ions recovered from oxalic acid leaching palygorskite-rich clay wastewater was used to construct the hydrotalcite-like composites, after adsorbing organic pollutants, which was calcined and carbonized to convert into the mixed metal oxide/carbon composites (MMO/Cs). The fabricated MMO/Cs showed outstanding adsorption performance for the anionic azo dye Congo Red (CR). Especially, the MMO/C2 with the M2+/M3+ molar ratio of 2, which adjusted by supplementing Mg2+, had ultra-high adsorption capacity and ultra-clean removal efficiency for CR. The adsorption capacity was as high as 3303 mg/g, and only 0.5 g/L MMO/C2 dosing treatment for 6 h could completely decolor and remove the 2000 mg/L CR aqueous solution. Moreover, MMO/Cs exhibited the ability to simultaneous remove CR and Methylene blue (MB) mixed dye contaminants, and demonstrated the excellent recyclability. This work provides a promising method for the high-value conversion of waste resources and the synthesis of high-efficiency adsorbents.

[Preparation of Mixed Metal Oxide/Carbon Composites and Its Adsorption Performance for Pb(â ¡)].

Layered double hydroxides, which can be synthesized from metal ions and their analogs, have abundant interlayer ions, surface functional groups, and adsorption characteristics that have been extensively studied. But the adsorption-desorption process may cause secondary pollution of the environment. In this study, the layered double hydroxides that adsorbed Congo red were converted into mixed metal oxide/carbon composites by a calcining carbonization method, and its adsorption performance for heavy metal ions Pb(Ⅱ) in aqueous solution was studied in detail. The results show that the prepared mixed metal oxide/carbon composites have a faster adsorption rate and higher adsorption capacity for Pb(Ⅱ). The adsorption capacity reached more than 150 mg·g-1 in 30 min, and increased with the content of Mg2+ introduced into the layered double metal hydroxide, reaching a maximum of 368 mg·g-1. The removal mechanism of Pb(Ⅱ) by mixed metal oxide/carbon composites was caused by the formation of insoluble Pb3(CO3) 2(OH) 2 on the surface. This research lays the foundation for the application of mixed metal oxide/carbon composites in the remediation of lead-containing soils.

An upgraded and universal strategy to reinforce chitosan/polyvinylpyrrolidone film by incorporating active silica nanorods derived from natural palygorskite.

Active silica nanorod (OPal) was prepared from natural palygorskite (RPal) using an updated acid leaching route, and then the effect of RPal and OPal as nano-filler on the network structure, mechanical, thermal and anti-aging properties of chitosan/polyvinylpyrrolidone (CS/PVP) films was studied comparatively. It was revealed that OPal had a better dispersibility than RPal in CS/PVP substrate, and its incorporation improved the mechanical properties and thermal stability of the films significantly. The optimal composite film containing OPal shows the maximum tensile strength of 27.53 MPa (only 14.87 MPa and 22.47 MPa for CS/PVP and CS/PVP/RPal films, respectively), resulting from the more uniform dispersion of OPal in polymer substrate and its stronger interaction with 3D polymer network. By a controllable acid-leaching process, the metal ions in octahedral sheets of RPal were dissolved out continuously, which is favorable to alleviate the adverse effects of variable metal ions on the film under UV light irradiation, and thus improve the aging-resistant ability of films. This study provides new ideas for improving the reinforcing ability of natural clay minerals towards biopolymer-based material, finds a new way to resolve the aging problem of polymer composites caused by incorporation of natural clay minerals.

Significantly improve the water and chemicals resistance of alginate-based nanocomposite films by a simple in-situ surface coating approach.

Biopolymers have shown great application prospects due to their advantages of being biodegradable, renewable, non-toxic, safe and inexpensive. However, the innate hydrophilicity of biopolymers means the materials prepared from them easily swell or disintegrate in aqueous media, limiting their applications. Herein, on the basis of improving the mechanical performance of a sodium alginate/poly(vinyl alcohol) (SA/PVA) film by introducing palygorskite (Pal) nanorods, the hydrophobicity of the obtained SA/PVA/Pal film was improved further by surface coating with methyltrichlorosilane (MTCS) through a vapor deposition-surface polycondensation reaction. MTCS nanofilaments, with a size of approximately 50 nm, were formed on the film surface by the silanization reaction between MTCS and hydroxyls, resulting in an improvement in surface hydrophobicity characterized by a contact angle (111.8°) higher than that of SA/PVA/Pal film (72.7°). Therefore, the obtained films maintained their original shape and strength after soaking for a long time in aqueous solutions containing acid, alkaline, and electrolyte, also in organics, while the uncoated film dissolved quickly and lost its original shape. Moreover, the surface coating also increased the film's tensile strength from 11.43 to 28.69 MPa. This demonstrates a simple, universal and effective way to improve the resistance of biopolymer-derived materials to water and various chemicals.

Optimal Synthesis of Environment-Friendly Iron Red Pigment from Natural Nanostructured Clay Minerals.

A series of environment-friendly clay minerals-α-Fe2O3 iron-red hybrid pigments-were prepared by a simple one-step hydrothermal reaction process using natural nanostructured silicate clay minerals as starting materials. The influence of structure, morphology and composition of different clay minerals on the structure, color properties, and stability of the pigments was studied comparatively by systematic structure characterizations with X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmittance electron microscope (TEM), X-ray fluorescence spectroscopy (XRF), X-ray photoelectron spectroscopy (XPS) and CIE-L*a*b* Colorimetric analyses. The results showed that the clay minerals act as green precipitants during the hydrothermal reaction to induce in-situ transformation of Fe(III) ions into Fe2O3 crystals. Meanwhile, they also act as the "micro-reactor" for forming Fe2O3 crystals and the supporter for inhibiting the aggregation of Fe2O3 nanoparticles. The color properties of iron-red hybrid pigments are closely related to the surface charges, surface silanol groups, and solid acid sites of clay minerals. The clay minerals with higher surface activity are more suitable to prepare iron-red pigments with better performance. The iron-red hybrid pigment derived from illite (ILL) clay showed the best red color performance with the color values of L* = 31.8, a* = 35.2, b* = 27.1, C* = 44.4 and h° = 37.6, and exhibited excellent stability in different chemical environments such as acid, alkaline, and also in high-temperature conditions.