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Aluminum (Al) powder is widely used in solid propellants. In particular, nano-Al has attracted extensive scholarly attention in the field of energetic materials due to its higher reactivity than micro-Al. However, the existence of aluminum oxide film on its surface reduces the heat release performance of the aluminum powder, which greatly limits its application. Hence, this paper used iron, a component of solid propellant, to coat micron-Al and nano-Al to improve the heat release efficiency and reactivity of Al powder. SEM, TEM, EDS, XRD, XPS, and BET were used to investigate the morphological structure and properties of pure Al and Fe/Al composite fuels of different sizes. The results show that Fe was uniformly coated on the surface of Al powder. There was no reaction between Fe and Al, and Fe/Al composite fuels had a larger specific surface area than pure Al, which could better improve the reactivity of pure Al. Besides, the catalytic effects of pure Al and Fe/Al composite fuels of different sizes on ammonium perchlorate and ammonium nitrate were explored. The results show that the catalysis of pure Al powder could be greatly improved by coating Fe on the surface of Al powder. Especially, the micron-Fe/Al composite fuel had a higher catalytic effect than the pure nano-Al powder. Hence, Fe/Al composite fuels are expected to be widely used in solid propellants.

Formation of super-hydrophobic and corrosion-resistant coatings can provide significant corrosion protection to magnesium alloys. However, it remains a grand challenge to produce such coatings for magnesium-lithium alloys due to their high chemical reactivity. Herein, a one-step hydrothermal processing was developed using a stearic-acid-based precursor medium, which enables the hydrothermal conversion and the formation of low surface energy materials concurrently to produce the super-hydrophobic and corrosion-resistant coating. The multiscale microstructures with nanoscale stacks and microscale spheres on the surface, as well as the through-thickness stearates, lead to the super-hydrophobicity and excellent corrosion resistance of the obtained coating.

In-situ incorporation of layered double hydroxides (LDH) nanocontainers into plasma electrolytic oxidation (PEO) coatings on AZ91 Mg alloy has been achieved in the present study. Fumarate was selected as Mg corrosion inhibitor for exchange and intercalation into the nanocontainers, which were subsequently incorporated into the coating. It was found that the thickness and compactness of the coatings were increased in the presence of LDH nanocontainers. The corrosion protection performance of the blank PEO, LDH containing PEO and inhibitor loaded coatings was evaluated by means of polarization test and electrochemical impedance spectroscopy (EIS). The degradation process and corrosion resistance of PEO coating were found to be greatly affected by the loaded inhibitor and nanocontainers by means of ion-exchange when corrosion occurs, leading to enhanced and stable corrosion resistance of the substrate.

In this research, a novel Ni-Co-metallic glass composite was fabricated and the effect of the co-deposition of Ni60Cr10Ta10P16B4 amorphous metallic glass powder (MGP) on the morphology and electrocatalytic properties of Ni–Co coatings was evaluated. The process was initiated by producing Ni60Cr10Ta10P16B4 via mechanical alloying of elemental powders using a planetary ball mill. Then, Ni–Co nanocomposite coatings were deposited on a copper substrate by the addition of different amounts of MGP via the electrodeposition method in a Watts bath. Then, the microstructure and chemical composition of the deposits were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) successively. The electrocatalytic performance of the coatings was evaluated in a methanol-containing alkaline (1 M NaOH) solution through cyclic voltammetry (CV). The enhancement of the electrocatalytic activity of Ni–Co coating through the co-deposition of MGP was observed. It was also concluded that the electrocatalytic properties of composite coatings are optimized when 7.5 g L−1 of MGP is added to the electroplating bath. Moreover, MGP was demonstrated to have altered the microstructure and the content of Co besides enhancing the roughness and specific surface of coatings.

Binder jetting (BJ) 3D printing is especially suitable for the fabrication of an orodispersible solid dosage form, as it is an efficient way to avoid the use of mechanical forces typical for compaction-based processes. However, one of the existing challenges related to pharmaceutical applications of BJ is the relatively high amount of binder needed in the primary powder to ensure the sufficient mechanical strength of printed products. In this study, a strategy based on pre-processing with a thin layer coating was explored. With this strategy, the matrix particles (lactose monohydrate) of the primary powder for BJ 3D printing were coated with the binder (polyvinylpyrrolidone, PVP). The investigated compositions of the primary powder contained PVP at three levels, namely, 10 %, 15% and 20% (w/w). The primary powder compositions were prepared with or without the coated lactose powder, and they were subsequently 3D BJ printed into oral solid products with paracetamol as a model active drug substance. The presence of coated lactose in the primary powder increased the interparticulate interactions in the BJ 3D printed products. Especially for the composition with a relatively small amount of binder (i.e., 10% and 15% w/w PVP in the primary powder), the use of coated particles significantly improved the resistance to crushing and decreased the disintegration time of printed products. In conclusion, thin layer coating is an effective way to pre-process primary powder particles for BJ 3D printing of oral solid products.

Fragments and blast waves generated by explosions pose a serious threat to protective structures. Experiments have shown that the single ballistic resistance or blast resistance of the steel plate improves significantly after coating polyurea. However, the dynamic response and structural design for the polyurea-coated structure under the combined fragments and blast loading are still lacking. In this paper, the impact resistance of polyurea-coated steel plate under complex dynamic loading is analyzed and designed for improving comprehensive ballistic and blast resistance using the newly established computational evaluating model. Firstly, according to the thickness and placement effects of the coating on the ballistic and blast resistance, the steel-core sandwich plates are designed, which are proved to own outstanding comprehensive ballistic and blast resistance. Besides, the distribution diagram of ballistic and blast resistance for different polyurea-coated steel plates is given to guide the design of protective structures applying in different explosion scenarios. Furthermore, the dynamic response of designed plates under two scenarios with combined fragments and blast loading is studied. The results show that the synergistic effect of the combined loading is significant. It reduces both the ballistic and blast resistance of the polyurea-coated steel plate and causes a more severe failure than the sum of the failures induced by the individual fragments and blast impact. Besides, the acting sequence of the fragments and blast affects the structural protective performance heavily. It is found that the first loading inducing structural large deformation or damage generally is dominant. In the scenario of fragments penetrating firstly, the excellent unit-thickness ballistic performance of the structural front part is strongly needed for improving the comprehensive ballistic and blast resistance. The analysis of dynamic response and structural design for the polyurea-coated steel plate in this paper will be helpful for designing lightweight protection structures with excellent comprehensive ballistic and blast resistance.

The study is aimed to utilize the silica fume coated plastic waste in the concrete in place of uncoated plastic waste. The main aim of the study is to evaluate the effect on fresh and mechanical properties of concrete after coating the plastic waste with mineral admixture i.e silica fume. The study of utilization of different kinds of plastics forms in concrete has been carried out earlier as well. The major concern is the bonding between concrete mix and the plastic by which the strength could not be attained as desired as per the grade. The present investigation is an endeavor to enhance the bonding characteristics of waste PET fibers with concrete mix by coating them with mineral admixture such as silica fumes by utilizing epoxy resins as an adhesive. The examination was done by utilizing waste PET fibers in aspect ratio AR 25 (50 mm נ2 mm), AR 50 (100 mm נ2 mm) and AR 75(150 mm/2 mm) and consolidate them as bond weight in separate interims of 3%, 6%, 9% and 12%. The modern and mechanical qualities of concrete mix investigated with incorporation of silica fume coated waste PET fibers and ordinary waste PET fibers were contemplated.

Solar cell layers technology has achieved global standing in the solar cell layers deposition process, and it covers the innovative methods and techniques in significant applications. Recent solar cell layers technology has an advanced interest in a refined approach to enhance performance and highlights the importance of recent proficient procedures for manufacturing. For example, the application is used to search for novel materials for solar cells' layers to clarify the current energy crisis. The technological process and various types of solar cells depend on climate change. Among them, layers of solar cells and silicon wafer solar cells are very encouraging. Solar cell layers technology has led to solar cells being a more reasonable active option in design and production. The productivities facilitated by new solar cells still need to be enhanced for the various processes involved in the additional enhancement from Copper Indium Gallium Selenide (CIGS) microfilms to solar cell crystal structure dye-sensitized solar cells. The hydrophobic coating works as an anti-dust coating, enhancing efficiency and decreasing the cost of cleaning solar cells. In Saudi Arabia Majmaah City, most solar projects are in dry regions, where the dusty weather reduces solar cell efficiency. Therefore, combining these two properties and applying an anti-reflective and superhydrophobic coating will increase solar cell efficiency by 20%. Solar cells' crystal structure results are substituted with layers or new materials to balance environmental impact and toxic nature.

In this study, Mg–6.0Zn–3.0Sn–0.5Mn (ZTM630) magnesium alloy was pre-activated by colloidal Ti, oxalic acid, and phosphoric acid, and a phosphate conversion coating (PCC) was prepared on the alloy surface. The morphology and corrosion resistance of the prepared PCCs were investigated. Surface morphology studies showed that the phosphate crystals that formed the coating were the smallest for the sample pre-activated by phosphoric acid. The coating on the colloidal Ti and the phosphoric acid samples had the largest and the smallest thickness and surface roughness, respectively. The reason for the discrepancy was analyzed by comparing the surface morphologies of alloy samples immediately after the pre-activation treatment and various phosphating treatments. X-ray diffraction analysis revealed that all three PCCs contained the same compounds. The corrosion resistance time from the copper sulfate drop test and the electrochemical data from the potentiodynamic polarization curves showed that the coating pre-activated by phosphoric acid had the best corrosion resistance. Finally, the 1500 h neutral salt spray corrosion test confirmed that the phosphating treated magnesium alloy, which was pre-activated by phosphoric acid, exhibited excellent corrosion resistance and behavior.

Photothermal therapy becomes a hotspot in the treatment of bone tumors. Magnesium and its alloys are regarded as potential bone implants for their favorable mechanical property and biodegradable in vivo. However, there is few research devoted to fabricating a photothermal coating on Mg alloy. In the present study, reduced graphene oxide coating with a strong photothermal effect was prepared on the surface of AZ31 via two steps. Firstly, graphene oxide coating was deposited on the surface via electrophoresis deposited (GO#), followed by a reduction process of the graphene oxide coating in ultrapure water (rGO#). GO# and rGO# coatings were characterized by SEM, Raman, XRD, FTIR, and XPS. The results revealed that, compared with GO# coating, the content of oxygen-containing (C O/C O-C, C=O, O C=O) groups on rGO# coating was significantly decreased. rGO# coating was found tightly adhered to AZ31 substrate. According to the first-principles calculations, the well-bonded heterostructure between MgO and rGO is the main reason for the strong bonding force. Moreover, the prepared rGO# coating showed a superior photothermal effect, which brings a new strategy to the treatment of bone tumors with Mg-based implants.

Protein adsorption preferentially occurs and significantly affects the physicochemical reactions once the biodegradable magnesium alloys as bone replacements have been implanted. To date, interactions mechanisms between Mg implants and proteins remain unclear at a molecular level. Thereby, a combination of molecular dynamic (MD) simulations and experimental exploration is used to investigate the adsorption behavior and conformational change of bovine serum albumin (BSA), a representative protein of blood plasma, upon the surface of micro-arc oxidation (MAO) coated Mg alloy AZ31. The influences of absorbed proteins on the cytocompatibility of MAO coating are evaluated by virtue of cytotoxicity assay. Results indicate that the negatively charged O atoms (BSA) exhibit strong interaction with Mg2+ ions of Mg(OH)2, revealing that BSA molecules are ionically adsorbed on the AZ31 surface. Interestingly, MD simulation reveals that MAO coating demonstrates superior ability to capture BSA molecules during the process of adsorption owing to strong electric attraction between the negatively charged O atoms in BSA molecules with Mg atoms of MgO in MAO coating. Moreover, the α-helix part of absorbed BSA molecules on AZ31 substrate and MAO coating markedly decreases with an increase in β-sheet, β-turn and unordered contents, which is attributed to the reduction in the number of hydrogen bonds in BSA molecules. Furthermore, the adsorbed BSA molecules improve the cytocompatibility of MAO coating since the positively charged -NH3+ group and β-sheet content of absorbed BSA molecules mediate the cell adhesion by interacting with the negatively charged cell membrane.

Superhydrophobic coating has been widely studied for its great applicational potential, such as for corrosion protection of magnesium alloys while it has been restrained by expensive materials, sophisticated preparation process and infirm rough structures. In this study, the electrochemical method was adopted by using a two-electrode system for rapid hydrophobic modification to obtain superhydrophobic kaolin. By mixing the modified superhydrophobic kaolin with commercial epoxy resin and polydimethylsiloxane glue, a paint can be formed and easily used on various substrates for preparation of superhydrophobic coating via spraying method. The influence factors on wettability of the modified kaolin and the mixing ratio of each component of the coating were explored. Also, the wettability, durability and anticorrosion of the prepared coating were evaluated comprehensively. The coating was able to maintain superhydrophobic after immersed in HCl solution at pH 1, the NaOH solution at pH 14, and 3.5 wt.% NaCl solution for 16, 21, 30 days, respectively. In addition, the coating exhibited 4A grade adhesion, high hydrophobicity after abraded for 200 cycles on a 600-mesh sandpaper with 100 g weight, and 99.86% anticorrosion efficiency after soaked in 3.5 wt.% NaCl solution for 20 days, demonstrating a good robustness and anti-corrosion property. Furthermore, the coating showed good transparency, flexibility and was easy to make in a large scale by the spraying method, which is of great significance to promote the practical application of superhydrophobic coatings and the anticorrosion Mg alloys.

ZrB2–SiC–HfB2–WC coating applied by spark plasma sintering led to the ablation resistance improvement of graphite substrate. The influence of HfB2/WC ratio was investigated on the ablation resistance produced by an oxyacetylene flame. The microstructural evolutions and phase characterization were studied using scanning electron microscopy and X-ray diffraction, respectively. It is confirmed that the ablation resistance of sample with 5% WC and 2.5% HfB2 was significantly increased with minimum ablated materials and rate of 1.1% and 2.2 mg s−1 employing the results of oxyacetylene flame test. The important mechanisms of improvement of the ablation resistance were the evaporation of WO3 and SiO upon oxidation of SiC and WC in the coating.

To improve the safety of HMX, HMX/NH2-GO composite was prepared with aqueous ammonia functionalized graphene oxide (NH2-GO). The composite was characterized by SEM, Zeta potential, XPS, Raman spectrum, XRD, HPLC, DSC and BAM sensitivity test. The results indicated that the functionalization with aqueous ammonia can enhance the interaction between GO and HMX, and more efficiently desensitize the explosive. The optimal impact sensitivity of the HMX/NH2-GO composite can be not less than 40 J, which is also the most insensitivity compared to the previous reports prepared by coating desensitization with non-energetic desensitized material. Moreover, the potential reason for the different impact and friction sensitivity was also discussed, which may bring a novel perspective to achieve the desensitization of energetic material.

International audience; Coatings with composition close to Ti3SiC2 were obtained on SiC substrates from Ti and Si powders with the molten NaCl method. In this work, the growth of coatings by reaction in the salt between monolithic SiC substrates and titanium powder is obtained between 1000 and 1200°C. At 1000°C, a coating of 8 µm thickness is formed in 10 hours whereas a thin coating of 0.5 µm has been grown in 2 hours. A lack in silicon was first found in the coatings prepared at 1100 and 1200°C. For these temperatures, the addition of silicon powder in the melt had a favorable effect on the final composition, which is found very close to the composition of Ti3SiC2. The reaction mechanism implies the formation of TiCx layers in direct contact with the SiC substrate and the presence of more or less important quantities of Ti3SiC2 and Ti5Si3Cx in the upper layers.; Des revêtements de composition proche de Ti3SiC2 ont été obtenus sur des substrats SiC à partir de poudres Ti et Si par la méthode du NaCl fondu. Dans ce travail, la croissance de revêtements par réaction dans le sel entre des substrats monolithiques SiC et de la poudre de titane est obtenue entre 1000 et 1200°C. A 1000°C, un revêtement de 8 µm d'épaisseur est formé en 10 heures alors qu'un revêtement fin de 0,5 µm a été développé en 2 heures. Un manque de silicium a d'abord été trouvé dans les revêtements préparés à 1100 et 1200°C. Pour ces températures, l'ajout de poudre de silicium dans le bain a un effet favorable sur la composition finale qui se retrouve très proche de la composition de Ti3SiC2. Le mécanisme réactionnel implique la formation de couches de TiCx en contact direct avec le substrat SiC et la présence de quantités plus ou moins importantes de Ti3SiC2 et Ti5Si3Cx dans les couches supérieures.

Novel hybrid coatings on pure magnesium were prepared by combining plasma electrolytic carburizing (PEC) with micro-arc oxidation (MAO) to further enhance the anti-corrosion property in this paper. Scanning electron microscopy (SEM) was used to observe the micro-structure of the coatings, meanwhile, energy dispersive spectrometry (EDS) and X-ray diffraction (XRD) were separately used to investigate the elemental as well as phase compositions of the coatings. The anti-corrosion property of the coatings was evaluated by potentiodynamic polarization curves as well as electrochemical impedance spectroscopy (EIS).The results show that PEC process is closely related with the effects of adsorption as well as diffusion of the activated carbon atoms, and it can provide a favorable pretreatment surface with predesigned chemical composition to obtain a new kind of phase, namely SiC with superior corrosion resistance and chemical stability, in the following PEC+MAO hybrid coatings. Meanwhile, PEC preprocessing also can afford an excellent micro-structure to increase the coating thickness as well as to improve the compactness of the PEC+MAO hybrid coatings. During the fabrication process of the PEC+MAO hybrid coatings, an overlapping phenomenon in regard to coating thickness can be observed instead of heaping up layer by layer. Compared with both single PEC surface modification layers as well as single MAO coatings, the PEC+MAO hybrid coatings exhibit more superior anti-corrosion property. Especially, the EIS data reveal that the PEC+MAO hybrid coatings can act as an effective protection system to provide relatively excellent long-range anti-corrosion protection. Note also that employing same MAO technique for both single MAO treatment as well as PEC+MAO combining procedure is the key to this research.

Epoxy resin powder coating has been successfully applied on the corrosion protection of magnesium lithium alloys. However, poor wear resistance and microcracks formed during the solidification have limited it extensive application. There are limited approaches to exploit such anti-corrosion and mechanical properties of magnesium lithium alloys. Herein, the epoxy resin powder coating with polydopamine modified molybdenum disulfide (MoS2@PDA-EP powder coating with 0, 0.1, 0.2, 0.5, 1.0 wt.% loading) was well prepared by melt extrusion to investigate its anticorrosion performance and wear resistance. The results revealed that the addition of MoS2@PDA enhanced the adhesion strength between coatings and alloys, wear resistance and corrosion protection of the powder coatings. Among them, the optimum was obtained by 0.2 wt.% MoS2@PDA-EP powder coating which could be attributed to well dispersion and efficient adhesion with coating matrix. To conclude, MoS2@PDA-EP powder coating is meaningfully beneficial for the anticorrosive and wear performance improvement of magnesium lithium alloys.

Multi-functionalization is the future development direction for protective coatings on metal surface, but has not yet been explored a lot. The effective integration of multiple functions into one material remains a huge challenge. Herein, a superhydrophobic multilayer coating integrated with multidimensional organic-inorganic components is designed on magnesium alloy via one-step plasma-induced thermal field assisted crosslinking deposition (PTCD) processing followed by after-thermal modification. Hard porous MgO ceramic layer and polytetrafluoroethylene (PTFE) nano-particles work as the bottom layer skeleton and filler components separately, forming an organic-inorganic multilayer structure, in which organic nano-particles can be crosslinked and cured to form a compact polymer-like outer layer with hierarchical surface textures. Remarkably, the chemical robustness after prolonged exposure to aqua regia, strong base and simulated seawater solution profits from polymer-like nanocomposite layer uniformly and compactly across the film bulk. Moreover, the self-similar multilayer structure coating endows it attractive functions of strong mechanical robustness (>100th cyclic rotary abrasion), stable and ultra-low friction coefficient (about 0.084), high-temperature endurance, and robust self-cleaning. The organic-inorganic multilayer coating also exhibits high insulating property with breakdown voltage of 1351.8 ± 42.4 V, dielectric strength of 21.4 ± 0.7 V/µm and resistivity of 3.2 × 1010 Ω·cm. The excellent multifunction benefits from ceramic bottom skeleton, the assembly and deposition of multidimensional nano-particles, and the synergistic effect of organic inorganic components. This study paves the way for designing next generation protective coating on magnesium alloy with great potential for multifunctional applications.

Boron is a very promising and highly attractive fuel because of high calorific value. However, the practical applications in explosives and propellants of boron have been limited by long ignition delay time and low combustion efficiency. Herein, nano-Al and graphene fluoride (GF) as surface activated materials are employed to coat boron (B) particles to improve ignition and combustion performance. The reaction heat of nano-Al coated B/KNO3 and GF coated B/KNO3 are 1116.83 J/g and 862.69 J/g, respectively, which are higher than that of pure B/KNO3 (823.39 J/g). The ignition delay time of B/KNO3 could be reduced through nano-Al coating. The shortest ignition delay time is only 75 ms for B coated with nano-Al of 8 wt%, which is much shorter than that of pure B/KNO3 (109 ms). However, the ignition delay time of B/KNO3 coated with GF has been increased from 109 to 187 ms. B coated with GF and nano-Al shown significantly influence on the pressure output and flame structure of B/KNO3. Furthermore, the effects of B/O ratios on the pressure output and ignition delay time have been further fully studied. For B/KNO3 coated with nano-Al and GF, the highest pressures are 88 KPa and 59 KPa for B/O ratio of 4:6, and the minimum ignition delay time are 94 ms and 148 ms for B/O ratio of 7:3. Based on the above results, the reaction process of boron coated with GF and nano-Al has been proposed to understand combustion mechanism.

In the preparation of plasma electrolytic oxidation (PEO) coating, the rapid heating of freely-happened electron avalanche under traditional discharge (TD) mode inevitably results in a strong eruption of electric breakdown melt. The PEO coating is loose and invariably composed of a very thin inner dense layer and an outer loose layer, as a result of which its properties and application have been limited greatly. In this work, for purpose of weakening the eruption of breakdown melt, thickening the inner dense layer, densifying the outer loose layer and improving the performance of PEO coating, ordinal discharge (OD) mode of PEO coating is developed by regulating the mass ratio of MgF2 to MgO (α) and voltage in the PEO investigation on AZ61 magnesium alloy in KF-KOH electrolyte. The formation mechanism under different discharge mode, electrochemical corrosion and wear of PEO coatings are investigated. The results show that the suitable α and voltage for effective OD are 1.3 and 130 V under which the freely-happened electron avalanche in MgF2 under TD mode can be restricted by the adequate adjacent MgO. Compared with TD mode, the inner dense layer, in which the ( 1 ¯ 0 1 ¯ ) plane of MgF2 is parallel to the (111) plane of MgO at their well-knit semi-coherent interface, is thickened to 2.4∼7.2 times, the corrosion potential (Ecorr) improvement is enlarged to 3.6∼13.2 times and the corrosion current intensity (Icorr) is reduced from 10.8∼9.499 to 0.433 (10−6 A/cm2). The outer loose layer is densified and the wear rate is lessened 65.5%∼89.8% by the evident melioration in surface porosity, impedance and hardness. This work deepens the understanding about the discharge of PEO coating and provides an available OD mode for preparing excellent PEO coating.

Ultrathin conversion coatings, made from aligned graphene derivatives and ammonium zirconium carbonate (AZC), were fabricated on stainless steel by electrodeposition. Sulfonated graphene oxide (SGO) provided electron pathways and physical barriers to corrosive molecules. Electrodeposition ensured the alignment of SGO and the facile fabrication of the coatings. AZC is an environmental-friendly crosslinking agent, water-repellent and corrosion inhibitor. Upon dehydration reactions, AZC improved the cohesion between SGO layers and anchored the conversion coatings on metal substrates. When the mass ratio of SGO to AZC was 2:1, the corrosion current density of the composite coatings reached 0.098 ​μA ​cm−2, while that of the bared stainless steel was 1.04 ​μA ​cm−2, given a coating thickness of only 500 ​nm. The electrical conductivity of SGO/AZC composite coatings can be tailored from 3.84 ​× ​10−5 to 2.28 ​× ​10−3 ​S‧cm−1 by heat treatment and HI reduction, which satisfied the electrical conductivity requirement of wide applications in electronic industry, office appliances and petroleum storage.

Poly(arylene sulfide sulfone)/graphene nanoplate (PASS/GNP) composites with segregated structure based on continuous polymer fiber skeletons were fabricated by coating a thin conductive layer on the PASS fibers and then performing compression molding. The formation of a unique segregated conductive network endowed the PASS/GNP composites with high electrical conductivity and excellent electromagnetic interference (EMI) shielding effectiveness (SE), reaching 17.8 ​S/m and 30.1 ​dB, respectively, when the content of the GNPs in the conductive layer was 20 ​wt%. The PASS/GNP composites also exhibited outstanding mechanical properties, which was attributed to the continuous PASS fiber skeletons that could withstand large loads and the strong interfacial interaction between the conductive layers and the PASS fibers that could provide good stress transfer. This approach is suitable for most soluble polymers.

High efficiency, environmental protection and sustainability have become the main theme of the development of the protection engineering, requiring that the components not only meet the basic functions, but also have chemical properties such as acid and alkali corrosion resistance and aging resistance. Polyisocyanate-oxazodone (POZD) polymer has the above characteristics, it also has the advantages of strong toughness, high strength and high elongation. The concrete slab sprayed with POZD material has excellent anti-blast performance. In order to explore the damage characteristics of POZD sprayed concrete slabs under the action of contact explosion thoroughly, the contact explosion test of POZD concrete slabs with different charges were carried out. On the basis of experimental verification, numerical simulation were used to study the influence of the thickness of the POZD on the blast resistance of the concrete slab. According to the test and numerical simulation results that as the thickness of the coating increases, the anti-blast performance of the concrete slab gradually increases, and the TNT equivalent required for critical failure is larger. Based on the above analysis, empirical expressions on normalized crater diameter, the normalized spall diameter and normalized spall diameter are obtained.

Plant mucilages have been used for many applications as stabilizers, emulsifiers, thickening or gelling agents, viscosity modifiers, encapsulating agents and food packaging materials (stand-alone films, coatings). In these studies, it has been reported that plant mucilages have potential to extend the shelf-life of food products when applied as coatings or packaging films by reducing the oxidative reactions, microbial spoilage. Besides, they exert required mechanical integrity, and/or barrier against water, and provide active properties as carriers of aroma compounds or antioxidant and antimicrobial agents. Along with their digestive health promoting activities, mucilages also can be used as a fat replacer to reduce the calorie of added food product. Acting as biopolymeric encapsulating agent, mucilages can protect antioxidant and antimicrobial compounds or retain viability of probiotic bacteria in gastrointestinal system with their controlled release properties. This review shows an overview of literature concerning the chemistry, extraction and recent uses of seed mucilage in food industry including encapsulation, emulsion/stabilization, edible film or coating applications, as well as their possible health benefits or employement for drug delivery purposes.

This work was made to investigate how nucleation and growth behavior of the coating film were affected by surface topographies of Mg–Al–Zn alloy substrate during the initial stage of plasma electrolytic oxidation (PEO). To satisfy this end, a single substrate was prepared by mechanical treatment exhibiting rough and smooth regions with an equal area on the surface. The rough region with prominent hills and grooves induced the breakdown of passive film, which was indicated by an early appearance of plasma discharge on the rough region since nucleation of coating film occurred preferentially around the hills. However, the coating film grown on the grooves was somewhat thicker and more porous than the film grown on the hills and smooth regions. This was due to the fact that the growth of the coating film was found to be localized in the presence of rough region, which was in line with the discharge activities. Herein, the nucleation and growth behavior during the initial stage of PEO will be discussed schematically on the basis of microstructural interpretation.

This study assessed the applicability of chitin nanocrystals prepared by 2, 2, 6, 6-Tetramethyl-1-Piperidine-1-oxyl radical (TEMPO)-mediated oxidation in traditional papermaking coating color systems. The α-chitin nanocrystals (CTNCs) with different carboxyl content, size, and morphology were prepared from crab shells by alkali pretreatment and TEMPO-mediated oxidation in the water at pH 10, and then the ratio of CTNCs to latex was applied to traditional coating color system to replace part of latex. The results showed that when the amount of NaClO added as co-oxidant in the oxidation was 15.0 mmol/g of chitin, the carboxyl content of alkali-pretreated CTNCs was up to 0.76 mmol/g. The amount of carboxyl groups presented a linear relation with the degree of individualization of nanocrystals and dispersion. When the ratio of latex to CTNCs was 90꞉10, the water retention value of the coating was 92% lower than that of the pure latex system, and the rheological property was better. The relationship between the addition amount of CTNCs and the surface strength and the coverage of coating layers were also studied, and results showed that when the ratio of latex to CTNCs was 95꞉5, the surface strength was the highest of 1.45 m/s, and the coverage of coating layers rate reached the highest of 78%.

Al-based MIL-53 MOF nanostructure was synthesized hydrothermally and then co-deposited in the electroless nickel coating on AM60B magnesium alloy using Zr pretreatment as an eco-friendly underlayer. The MIL-53(Al) nanostructure was synthesized in the form of layered semi-cube crystals with the surface area and mean pore diameter of 985.72 m2g−1 and 2.00 nm, respectively. The SEM images captured with two various zooming scales from the surface of the plain and MOF containing electroless layers showed cauliflower-like morphology with even distribution of nodule size. Also, the sub-grains of the plain coating disappeared after incorporation of the MOF. Although, both the normal and nanostructure-containing electroless layers have crystalline-amorphous structure, but the nanocomposite coating showed less crystallinity. The average surface roughness of the plain electroless coating was about 309 nm, which decreased to about 222 nm after incorporation of the MOF. The XRD patterns showed that the characteristic peak of Ni broadened after incorporation of the MOF, probably due to the decreasing of the crystallinity. For the heat-treated normal and MOF containing coatings at 200 °C no phase transition takes place, but new peaks appeared for heat-treated coatings at 400 °C due to the crystallization and second-phase precipitation. The results of the EIS tests showed an increase in the amount of the charge transfer resistance (from 19 to 29 kΩ cm2) after addition of the MOF, which means an improvement in the corrosion resistance. Also, low Jcorr of the composite coating represents its higher corrosion resistance with respect to the plain coating. The micro-hardness values of the composite coating before and after the heat treatment were higher than the plain coating. Also, the Ni-P-MOF coating has a lower wear rate both before and after the heat treatment due to an improvement in its micro-hardness.

Biodegradable magnesium alloys have excellent properties with respect to biodegradability, biocompatibility, and biomechanics, which may indicate a possibility of its application in intestinal stents. Investigation of Mg-Zn-Y-Nd alloy's application in intestinal stents has been performed. This study aims to investigate the degradation behavior of Mg-Zn-Y-Nd alloy intestinal stents coated with poly(L-lactide)/paclitaxel in the intestinal environment and its biocompatibility with intestinal tissue. In this paper, Mg-Zn-Y-Nd alloy's corrosion properties were evaluated by the immersion test in human feces, SEM and XRD, and animal tests. In vitro results showed that when the Mg-Zn-Y-Nd alloy was immersed in human feces for two weeks, its corrosion resistance could be improved by micro arc oxidation (MAO) and poly-l-lactide (PLLA) dual coating. Additionally, this result was also confirmed in vivo experiments by rabbit model. And animal tests also demonstrated that the Mg-Zn-Y-Nd alloy with MAO/PLLA/paclitaxel dual coating drug-eluting stents could inhibit the proliferation of local intestinal tissue around the stents. However, in vivo studies illustrated that the intestinal stents gradually degraded in rabbit model within 12 days. Considering the degradation rate of the stent was faster than expected in rabbits, the support performance of the scaffold requires further improvement.

Abstrct Polycaprolactone/hydroxyapatite (PCL/HA) composite coating was fabricated by a combination of hydrothermal and dipping methods to delay the degradation of Mg alloy AZ31 as bioresorbable materials. The PCL/HA coating was composed of nano rod-shape HA crystals and PCL filled in the space of HA crystals. Compared with the single HA coating, the binding strength between the PCL/HA composite coating and Mg alloy was obviously improved and the PCL/HA coating still adhered to the surface of AZ31 substrate even after 38 days of immersion. The electrochemical corrosion rate of HA coated sample was reduced by ten times after being filled by PCL. The electrochemical impedance spectroscopy (EIS) and immersion test results showed that the PCL/HA composite coating could provide a more effective barrier for Mg substrate than the HA coating alone. The cytocompatibility and the antibacterial property of HA coating and PCL/HA coating were evaluated by culturing with bone marrow-derived mesenchymal stem cells (BMSCs) and methicillin-resistant staphylococcus aureus (MRSA) for 24 h under direct culture conditions, respectively. The PCL/HA composite coating showed better BMSC cell compatibility, more suitable for BMSC adhesion than HA coating alone and showed a potential application prospect as a biological materials. However, from the perspective of clinical applications, the antibacterial property of PCL/HA composite coating needs to be further improved.

Chitosan-coated Fe3O4 nanoparticles were prepared by coprecipitation followed by reaction with chitosan and different volumes of glutaraldehyde. Coating was modified by varying the volume of glutaraldehyde and reaction time. XRD pattern shows maxima compatible Fe3O4 structure. FTIR spectroscopia confirms the presence of chitosan, more evident in samples with higher chitosan content, as denoted by TGA. TEM images of samples with low glutaraldehyde content reveal particles coated with a homogeneous chitosan shell. Meanwhile, those prepared with high glutaraldehyde volume show nanoparticles dispersed in an organic matrix. Samples present almost superparamagnetic behavior with magnetization saturation values that are reduced as the content of organic matter increases. Regarding the stability of these samples in solution, the presence of a homogeneous coating improves the initial suspension, although it does not prevent its subsequent aggregation over time. However, this aggregation process is reduced for sample synthesized with 1 mL of glutaraldehyde after 6 h of reaction.

Plasma electrolytic oxidation (PEO) is a promising surface treatment to generate adherent and thick anti-corrosive coating on light-weight metals (Al, Mg, Ti, etc.) using an eco-friendly alkaline electrolyte. High energy plasma, however, inevitably generates porous structures that limit their practical performance. The present study proposes a straight-forward simple method by utilizing sub-zero electrolyte (268 K) to alter the plasma characteristics during formation of the protective coating on AZ31 Mg alloy via PEO with a comparison to the electrolyte at room temperature (298 K). In refrigerated electrolyte, the formation of micro-defects is suppressed relatively at the expense of low coating growth, which is measured to be twice lower than that at 298 K due to the temperature-dependent soft plasma discharges contributing to the development of the present coating. As a consequence, corrosion resistance of the sample processed at 268 K is superior to that of 298 K, implying that the effect of coating thickness is less dominant than that of compactness. This phenomenon is interpreted in relation to the ionic movement and oxide solidification controlled by soft plasma discharges arising from the temperature gradient between electrolyte and surface of the substrate during PEO.

This work is based on the development of a stacked AISI 304 stainless steel wire meshes structure with oxidizing and filtering capacity, where the Co and Ce oxide catalysts were deposited on the surface of the metallic fibres as a novel alternative to the current DOC – DPF system. The system was scaled up encouraged by the results obtained at lab scale, going from 16 mm filter diameter to 130 mm. The coated meshes were stacked inside a metallic case in order to conform a catalysed diesel particulate filter (CDPF). A Fiat Palio diesel engine mounted on a test bench was used to evaluate the filtering capacity of the scaled-up wire mesh cartridge. The systems developed were able to reduce particulate matter emitted by diesel engines below limits restrained by laws. The good activity, pressure drop, robustness, versatility and low cost of the designed structures, along with the good adhesion of the catalytic coating, makes them very promising for the development of catalytic filters.

To produce nanocomposite materials with high magnetic properties, studies concerning on nanostructural processing technologies and control mechanisms are urgently required in aspects of achieving perfect alignment of the hard phase while keeping desired sizes and distributions of the soft phase. In the present study, a designed low-rate electroless deposition method is found to be an effective way in producing strong textured anisotropic Sm-Pr-Co/Co nanocomposites with unusual continuous soft-phase coatings when assembling Co particles on the ball-milled anisotropic Sm-Pr-Co hard phase. The average particle size of the soft-phase coatings is 18–50 nm and the obtained Sm-Pr-Co/Co composites exhibit a high intrinsic coercivity of Hci=748 kA/m with an enhanced remanence of Mr=79 A·m2/g, as compared to Hci=836 kA/m and Mr=68 A·m2/kg for uncoated Sm-Pr-Co hard phase. Moreover, the coating process study reveals a nucleation control mechanism for the formation of the continuous coating structures. Down-sized Sm-Pr-Co/Co nanocomposites with tailored size below 300 nm or even below 100 nm were also produced by this designed method. This study is of theoretical and practical importance for developing advanced nanostructures including the next generation permanent magnets.

Transition metal selenides attract significant attention as advanced anode materials for sodium-ion batteries (SIBs) in recent years due to their appropriate working potential and high theoretic capacity. However, the poor structural stability and rate capability limit their further practical applications. Herein, zeolite imidazole framework-8/zeolite imidazole framework-67 is used as a template to prepare Co0.85Se and ZnSe nanoparticles embed in N-doped carbon matrix successfully, and then coated a carbon layer (ZCS@NC@C) by in-situ polymerization. One side, the N-doped carbon matrix with rich pore structure not only shorten the diffusion path of Na+ and improve the conductivity of the electrode, but also prevent structural collapse and agglomeration of active particles during the sodium insertion/extraction process. On the other side, the carbon shell preparation by coating can form a protective layer to buffer the volumetric stress generated in the electrochemical process and further improve the electrical conductivity. As a result, the as-prepared ZCS@NC@C anode material exhibits an excellent electrochemical performance for SIBs. This investigation provides a promising approach to optimize the electrochemical performance of SIBs by incorporating active metal compounds into conductive carbons to form multidimensional structure.

Fabrication of selective adsorption coatings plays a crucial role in solid-phase microextraction (SPME). Herein, new strategies were developed for the in-situ fabrication of novel cobalt-based carbonaceous coatings on the nickel-titanium alloy (NiTi) fiber substrate using ZIF-67 as a precursor and template through the chemical reaction of ZIF-67 with glucose, dopamine (DA) and melamine, respectively. The adsorption performance of the resulting coatings was evaluated using representative aromatic compounds coupled to high-performance liquid chromatography (HPLC) with ultraviolet detection (HPLC-UV). The results clearly demonstrated that the adsorption selectivity was subject to the surface elemental composition of the fiber coatings. The cobalt and nitrogen co-doped carbonaceous coating showed better adsorption selectivity for ultraviolet filters. In contrast, the cobalt-doped carbonaceous coating exhibited higher adsorption selectivity for polycyclic aromatic hydrocarbons. The fabricated fibers present higher mechanical stability and higher adsorption capability for model analytes than the commercial polydimethylsiloxane and polyacrylate fibers. These new strategies will continue to expand the NiTi fibers as versatile fiber substrates for metal-organic frameworks (MOFs)-derived coating materials with controllable nanostructures and tunable properties.

In this work, the microstructure of titania coating fabricated on the surface of hydrostatically extruded titanium grade 4 with the use of the micro-arc oxidation method was studied. The surface topography and microstructure investigations performed with atomic force microscopy and scanning and transmission electron microscopy revealed that, by using an Na2HPO4 electrolyte, a well-adherent porous coating is produced on the top surface and side walls of the extruded rod. The distribution of chemical elements was analyzed by using energy dispersive X-ray spectroscopy. The chemical elements dissolved in the electrolyte i.e. (Na, P and O) incorporated into the coating. Sodium locates preferentially in the outer part of the coating, while phosphorus and oxygen are distributed throughout the whole coating. The most relevant finding shows that a grain refinement caused by a hydrostatic extrusion provoked an increase in density of high-angle grain boundaries (HAGB), which in turn secured the formation of a continuous amorphous layer close to the substrate. The presence of this layer compensates for the effect of anisotropic substrate, producing a comparable and homogenous microstructure with a large number of micropores.

Implant-associate infection (IAI) is a major cause of failure of bone implant materials, and one of the significant challenges in clinical managements. A synergistic coating strategy combining montmorillonite (MMT) sustained release, adsorption of bacteria and gentamicin (GS) bactericidal is proposed herein to tackle infection issues. Surface morphology, microstructure and chemical composition of the samples were investigated using SEM, XRD, FT-IR and XPS. Electrochemical experiments and immersion experiments reveal that corrosion resistance of Mg samples with GS/MMT coatings was higher than that of bare Mg alloy substrate in DMEM solution. In vitro studies demonstrated that the GS/MMT coating had a significant inhibitory effect on Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). The viability of MC3T3-E1 cells was 92.7% after a co-culturing for 72 h. After a subcutaneous transplantation of 90 days, the survival rate was 100% for GS/MMT-coated Mg alloy specimens with no infection at the implantation sites and no toxic damage to liver, kidney and local muscles pathological sections. This study provides a novel method for the preparation of sustained-release antimicrobial coatings on biodegradable Mg alloys as promising candidates for orthopedic implant materials.

The cerium conversion coating (CeCC) containing copper and manganese cations was applied to the galvanized steel. The microstructure and the composition of specimen were analyzed by field emission scanning electron microscopy (FE-SEM) and energy dispersive spectroscopy (EDS). Electrochemical impedance spectroscopy (EIS) and polarization tests were conducted in 3.5 wt% NaCl solution to investigate the coating corrosion resistance. The results show that there are improvements in corrosion resistance and microstructure of CeCC containing copper and manganese cations but copper ions increase corrosion resistance of CeCC from 5800 to 27000 Ω⋅cm2.

Highly transparent and super-wettable nanocoatings for multifunctional applications with outstanding physical properties are in high demanded. However, such nanocoatings resistant to water invasion and Ultraviolet (UV) weathering remain a significant challenge. In this work, physically durable coatings based on inorganic nanoparticles (NPs) and an organic segment (isocyanate-silane modified surfactant) have been synthesized via a sol-gel approach. It is noteworthy the isocyanate-silane with –NH–C O- functional group creates a strong bonding between the highly hydrophilic surfactant and the inorganic NPs. This in-house synthesized organic segment can render the coating long-lasting wetting properties and resist to be washed away by water, while the inorganic NPs can form sturdy covalent bonds with the nano-scale hierarchical structure on the glazing substrate to improve the durability. This nanocoating demonstrates high transparency with superwetting property (water contact angle, WCA ​= ​4.4 ​± ​0.3°), effective de-frosting performance. Water invasion or UV accelerated weathering tests do not significantly affect the self-cleaning performance of nanocoating. Physical properties, including coating adhesion, hardness, Young's modulus, and abrasion resistance are systematically investigated. Interestingly, this clear coating shows prominent infrared shielding property attributed to Antimony-doped tin oxide (Sb-doped SnO2) NPs. The developed nanocoating process is easy to scale up for larger areas that require multipurpose self-cleaning functions.

A silicon carbide (SiC) protective coating has been developed for dental ceramics, but whether the coated ceramics can match the classical VITA shades is unclear.The purpose of this observational in vitro study was to evaluate the color adaptability of SiC-coated dental ceramics by testing the hypotheses that SiC-coated disks can be fabricated to match standard tooth shades and have a perceptible color match rate of at least 50% for disks with a color difference (ΔE)2.0. The effects of ΔE, shade hue, shade value, observer sex, years of experience, profession, and shade guide orientation on color perception were studied.SiC-coated disks were fabricated to color match (ΔEA significant difference in color match rate was found between disks with ΔE2.0 (63.9%) and ΔE≥2.0 (41.7%) (P.001). Arranging shade by value (72.2%) instead of hue (67.2%) produced better color matching (P.001). Sex (P=.430), profession (P=.708), and years of experience (P=.902) had no significant influence on color matching.SiC-coated disks were successfully fabricated to match all VITA classical shades, and clinical visual color matching results confirmed that ΔE was a useful metric in optimizing color matching for the SiC-coated dental ceramics.

Defining and visualizing the three-dimensional (3D) structures of pharmaceuticals provides a new and important tool to elucidate the phenomenal behavior and underlying mechanisms of drug delivery systems. The mechanism of drug release from complex structured dosage forms, such as bilayer osmotic pump tablets, has not been investigated widely for most solid 3D structures. In this study, bilayer osmotic pump tablets undergoing dissolution, as well as after dissolution in a desiccated solid state were examined, and visualized by synchrotron radiation micro-computed tomography (SR-μCT). In situ formed 3D structures at different in vitro drug release states were characterized comprehensively. A distinct movement pattern of NaCl crystals from the push layer to the drug layer was observed, beneath the semi-permeable coating in the desiccated tablet sample. The 3D structures at different dissolution time revealed that the pushing upsurge in the bilayer osmotic pump tablet was directed via peripheral “roadways”. Typically, different regions of the osmotic front, infiltration region, and dormant region were classified in the push layer during the dissolution of drug from tablet samples. According to the observed 3D microstructures, a “subterranean river model” for the drug release mechanism has been defined to explain the drug release mechanism.

Here we demonstrate a theory-driven, novel dual-shell coating system of Li2SrSiO4 and Al2O3, achieved via a facile and scalable sol-gel technique on LiCoO2 electrode particles. The optimal thickness of each coating can lead to increased specific capacity (∼185 mAh/g at 0.5 C-rate) at a cut-off potential of 4.5 V, and greater cycling stability at very high C rates (up to 10 C) in half-cells with lithium metal. The mechanism of this superior performance was investigated using a combination of X-ray and electron characterization methods. It shows that the results of this investigation can inform future studies to identify still better dual-shell coating schemes, achieved by such industrially feasible techniques, for application on similar, nickel-rich cathode materials.