Fabrication and Thermal Conductivity Improvement of Novel Composite Adsorbents adding with Nanoparticles

Thermal conductivity is one of key parameters of adsorbents, which will affect the overall system performance of adsorption chiller. To improve adsorbent＇s thermal conductivity is always one of research focuses in chemisorption field. A new chemical composite adsorbent is fabricated by adding carbon coated metal（Aluminum and Nickel） nanoparticles with three different addition amounts into the mixture of chloride salts and natural expanded graphite aiming to improve the thermal conductivity. The preparation processes and its thermal conductivity of this novel composite adsorbent are reported and summarized. Experimental results indicate that the nanoparticles are homogenously dispersed in the composite adsorbent by applying the reported preparation processes. The thermal conductivity of the composite adsorbent can averagely enlarge by 20% when the weight ratio of the added nanoparticles is 10 wt%. Moreover, carbon coated aluminum nanoparticles exhibit more effective enlargement in thermal conductivity than nickel nanoparticles. As for the composite adsorbent of CaCl2-NEG, there is a big reinforcement from 30% to 50% for Al@C nanoparticles, however only 10% in maximum caused by Ni@C nanoparticles. The proposed research provides a methodology to design and prepare thermal conductive chemical composite adsorbent.

Synthesis and characterization of carbon-coated cobalt ferrite nanoparticles

Cobalt ferrite nanoparticles（CFNPs） were prepared via a reverse micelle method. The CFNPs were subsequently coated with carbon shells by means of thermal chemical vapor deposition（TCVD）. In this process, acetylene gas（C2H2） was used as a carbon source and the coating was carried out for 1, 2, or 3 h at 750℃. The Ar/C2H2 ratio was 10：1. Heating during the TCVD process resulted in a NP core size that approached 30 nm; the thickness of the shell was less than 10 nm. The composition, structure, and morphology of the fabricated composites were characterized using X-ray diffraction, simultaneous thermal analysis, transmission electron microscopy, high-resolution transmission electron microscopy, and selected-area diffraction. A vibrating sample magnetometer was used to survey the samples＇ magnetic properties. The deposited carbon shell substantially affected the growth and magnetic properties of the CFNPs. Micro-Raman spectroscopy was used to study the carbon coating and revealed that the deposited carbon comprised graphite, multiwalled carbon nanotubes, and diamond-like carbon. With an increase in coating time, the intensity ratio between the amorphous and ordered peaks in the Raman spectra decreased, which indicated an increase in crystallite size.

Research on PbS Nanoparticles Coated with 2,6-O-Diallyl-β-CD

PbS nanoparticles coated with 2.6-O-dial1yl-β-CD were prepared successfully and characterized by transmission electron microscope (TEM), X-ray photoelectron spectrometer (XPS). The sample shows a very rapid induced absorption

Preparation and Control of the Formation of Single Core and Clustered Nanoparticles for Biomedical Applications Using a Versatile Amphiphilic Diblock Copolymer

We report the application of a versatile diblock copolymer,poly(ethylene oxide)-b-poly(γ-methacryloxypropyl trimethoxysilane)(PEO-b-PγMPS),to prepare nanocrystals such as iron oxide nanoparticles or quantum dots,with either a single core or multi-core cluster,for biomedical applications.This amphiphilic copolymer comprises both a hydrophilic PEO segment and a hydrophobic segment with a“surface anchoring moiety”(the silane group)which can interact effectively with the hydrophobic nanocrystals through ligand exchange.One of the unique features of this work is that we can control the formation of either single core nanoparticles or multi-core nanoclusters by simply varying the conditions of ligand exchange and aging of the mixture of block copolymer and nanoparticles without needing to change the copolymer.The morphologies of the resulting single core nanoparticles or multi-core nanoclusters were confirmed by dynamic light scattering and transmission electron microscopy.The clustered nanoparticles exhibit enhanced physicochemical properties that are beyond those expected from a simple accumulation of individual nanoparticles.Additionally,the hybrid nanoparticles containing both magnetic iron oxide nanoparticles and optical quantum dots obtained using our strategy provide have combined magnetic and optical functionalities that allow for potential new and expanded biomedical applications,as demonstrated by their use for magnetic resonance imaging and biomarker-targeted cell imaging.

Catheters coated with Zn-doped CuO nanoparticles delay the onset of catheter-associated urinary tract infections

Catheter-associated urinary tract infections （CAUTIs） are among the most common bacterial infections associated with medical devices. In the current study, the synthesis, coating, antibiofilm properties, and biocompatibility of urinary catheters coated with Zn-doped CuO （Zn0.12Cu0.880） nanoparticles （NPs） were examined. The doped NPs were synthesized and subsequently deposited on the catheter by the sonochemical method. The coated catheters displayed high antibiofilm activity and promising biocompatibility, as indicated by low in vitro cytotoxicity, negligible associated cytokine secretion, and absence of detectable irritation. The biocompatibility and ability of the Zn-doped CuO coating to inhibit biofilm formation were also evaluated in vivo using a rabbit model. Rabbits catheterized with uncoated catheters scored positive for CAUTI by day 4 of the experiment. In contrast, rabbits catheterized with Zn-doped CuO-coated catheters did not exhibit CAUTI until day 7 or remained completely uninfected for the whole duration of the 7-day experiment. Furthermore, the in vivo biocompatibility assays and examinations supported the biosafety of Zn-doped CuO-coated catheters. Taken together, these data highlight the potential of Zn-doped CuO nanocomposite as effective antibiofilm compound.

Recent development and challenges in enhancing fire performance on wood and wood-based composites:A 10-year review from 2012 to 2021

Due to their durability,versatility,and aesthetic value,wood and wood-based composites are widely used as building materials.The fact that these materials are flammable,however,raises a major worry since they might cause fire hazards and significant loss of life and property.The article investigates the variables that affect fire performance as well as the various fire-retardant treatments and their mechanisms.The current developments and challenges in improving the fire performance of wood and wood-based composites treated with fire-retardant materials are summarized in this paper.Nanoparticles,organic chemicals,and densification are some recent developments in fire-retardant treatments that are also emphasized.Key points from the review are summarized,along with potential areas for further research and development.

Large scale synthesis of FeS coated Fe nanoparticles as reusable magnetic photocatalysts

The FeS coated Fe nanoparticles were prepared by using high temperature reactions between the commercial Fe nanoparticles and the S powders in a sealed quartz tube. The simple method developed in this work is effective for large scale synthesis of FeS/Fe nanoparticles with tunable shell/core structures, which can be obtained by controlling the atomic ratio of Fe to S. The structural, magnetic and photocatalytic properties of the nanoparticles were investigated systematically. The good photocatalytic performance originating from the FeS shell in degradation of methylene blue under visible light and the high saturation magnetization originating from the ferromagnetic Fe core make the FeS/Fe nanoparticles a good photocatalyst that can be collected and recycled easily with a magnet. An exchange bias up to tl mT induced in Fe by FeS was observed in the Fe/FeS nanoparticles with ferro/antiferromagnetic interfaces. The enhanced coercivi- ty up to 32 mT was ascribed to the size effect of Fe core.

Effects of MgO modified β-TCP nanoparticles on the microstructure and properties of β-TCP/Mg-Zn-Zr composites

The mechanical properties and corrosion resistance of magnesium alloy composites were improved bythe addition of MgO surface modified tricalcium phosphate ceramic nanoparticles (m-β-TCP). Mg-3Zn-0.8Zr composites with unmodified (MZZT) and modified (MZZMT) nanoparticles were produced byhigh shear mixing technology. Effects of MgO m-β-TCP nanoparticles on the microstructure, mechanicalproperties, electrochemical corrosion properties and cytocompatibility of Mg-Zn-Zr/β-TCP compositeswere investigated. After hot extrusion deformation and dynamic recrystallization, the grain size ofMZZMT was the half size of MZZT and the distribution of m-β-TCP particles in the matrix was moreuniform than β-TCP particles. The yield tensile strength (YTS), ultimate tensile strength (UTS), andcorrosion potential (Ecorr) of MZZMT were higher than MZZT;the corrosion current density (Icorr) ofMZZMT was lower than MZZT. Cell proliferation of co-cultured MZZMT and MZZT composite sampleswere roughly the same and the cell number at each time point is higher for MZZMT than for MZZTsamples.

Sub-100 nm hollow SnO_2@C nanoparticles as anode material for lithium ion batteries and significantly enhanced cycle performances

Rational designing and controlling of nanostructures is a key factor in realizing appropriate properties required for the high-performance energy fields. In the present study, hollow Sn O2@C nanoparticles（NPs） with a mean size of 50 nm have been synthesized in large-scale via a facile hydrothermal approach.The morphology and composition of as-obtained products were studied by various characterized techniques. As an anode material for lithium ion batteries（LIBs）, the as-prepared hollow Sn O2@C NPs exhibit significant improvement in cycle performances. The discharge capacity of lithium battery is as high as 370 m Ah g 1, and the current density is 3910 m A g 1（5 C） after 573 cycles. Furthermore, the capacity recovers up to 1100 m Ah g 1at the rate performances in which the current density is recovered to 156.4 m A g 1（0.2 C）. Undoubtedly, sub-100 nm Sn O2@C NPs provide significant improvement to the electrochemical performance of LIBs as superior-anode nanomaterials, and this carbon coating strategy can pave the way for developing high-performance LIBs.

Assessing the effects of surface-bound humic acid on the phototoxicity of anatase and rutile TiO_2 nanoparticles in vitro

In this study,the cytotoxicity of two different crystal phases of TiO2 nanoparticles,with surface modification by humic acid（HA）,to Escherichia coli,was assessed.The physicochemical properties of TiO2 nanoparticles were thoroughly characterized.Three different initial concentrations,namely 50,100,and 200 ppm,of HA were used for synthesis of HA coated TiO2 nanoparticles（denoted as A/RHA50,A/RHA100,and A/RHA200,respectively）.Results indicate that rutile（LC50（concentration that causes 50%mortality compared the control group）=6.5）was more toxic than anatase（LC50=278.8）under simulated sunlight（SSL）irradiation,possibly due to an extremely narrow band gap.It is noted that HA coating increased the toxicity of anatase,but decreased that of rutile.Additionally,AHA50 and RHA50had the biggest differences compared to uncoated anatase and rutile with LC50of 201.9 and21.6,respectively.We then investigated the formation of reactive oxygen species（ROS）by TiO2 nanoparticles in terms of hydroxyl radicals（OH）and superoxide anions（O2^-）.Data suggested that O2^- was the main ROS that accounted for the higher toxicity of rutile upon SSL irradiation.We also observed that HA coating decreased the generation of OH and O2^- on rutile,but increased O2^- formation on anatase.Results from TEM analysis also indicated that HA coated rutile tended to be attached to the surface of E.coli more than anatase.

Plasma electrolytic oxidation of the magnesium alloy MA8 in electrolytes containing TiN nanoparticles

The formation of protective multifunctional coatings on magnesium alloy MA8 using plasma electrolyt- ic oxidation （PEO） in an electrolytic system containing nanosized particles of titanium nitride was investigated. Electrochemical and mechanical properties of the obtained layers were examined. It was established that microhardness of the coating with the nanoparticle concentration of 3 gl-1 increased twofold （4.2 ± 0.5 GPa）, while wear resistance decreased （4.97 × 10-6 mm3 N-1 m-1）, as compared to re- spective values for the PEO-coating formed in the electrolyte without nanoparticles （2.1 ± 0.3 GPa, 1.12 × 10.5 mm3 N-1 m-1）.

Flow properties of fine powders in powder coating

Three types of nanoparticles and their combinations were blended into a fine powder, which has been used in the powder coating industry. To study their effects on flow properties, the modified powder samples were characterized using a variety of techniques that tested the powder under different powder states ranging from dynamic to static. It was found that all three nanoparticles improved the flow properties of the powder to some degree, though the amounts of the nanoparticles needed were different depending on their physical properties. Secondly, inconsistency among these powder characterization techniques was also found. This is attributed to the different states of the powder samples during a measurement including dynamic, dynamic-static and static states. It was confirmed that characterization techniques which test the flow properties of a powder under all three states are needed to fully describe the flow properties of the powder. Finally, the effects of combinations of nanoparticles were explored, and it was found that combinations of nanoparticles can intensify, weaken or combine the effects of their component nanoparticles. The effects of nanoparticle combinations are not a simple summation of the effects of their comnonent nanoparticles.

Fabrication of a superamphiphobic coating by a simple and flexible method

A facile and flexible method to prepare raspberry-like nanoparticles that can be used as a superamphipho- bic coating is reported. Anatase TiO2 nanoparticles were chosen as the core because of their irregular morphology and photocatalytic performance. Anatase TiO2 nanoparticles were surrounded tightly by tiny functional fluoride-silica nanoparticles via the hydrolysis-condensation reaction of tetraethoxysi- lane and IH, 1H, 2H, 2H-perfluorodecyl triethoxysilane. The obtained Si-F@TiO2 nanoparticles can be sprayed or dipped directly onto various substrates. The coated film exhibited quite good liquid resistance, even when subjected to water jetting and sand abrasion. The photocatalytic effect of the coated anatase TiO2 with respect to formaldehyde was also studied and discussed. This method will provide more opportunities and fast access to practical applications in surface, environmental, and energy engineering.

Effect of Temperature on Thermal Treatment of Silica Coated Magnetic Nanoparticles

In the quest for developing a catalyst with as many desired characteristics, a facile synthetic route was designed for the preparation of mesoporous silica coated magnetic nanoparticles（MSMNP） employing a colloid mill reactor. The composite particles were characterized by the techniques, such as nitrogen adsorption-desorption isotherms, scanning electron microscopy（SEM）, transmission electron microscopy（TEM）, X-ray diffraction patterns （XRD）, thermo-gravimetric analysis（TGA）, Fourier transform infrared spectroscopy（FTIR） and vibrating sample magnetometer（VSM）, etc. The analysis showed that the resulted MSMNP composites were composed of silica shell layers with open pores connecting channels and NiFe204 with spinel structure, so the thermal treatment temperature did not show significant effect on pore textural properties, and its specific surface areas were in the range of 443-- 474 m2/g, while pore volume of about 0.8 cm3/g with an average pore size of around 9.5 nm. The composites with super paramagnetic nature were encapsulated entirely with amorphous silica layers contributing to optimum porosity and abundant surface hydroxyl groups.

Cytokine nanosponges suppressing overactive macrophages and dampening systematic cytokine storm for the treatment of hemophagocytic lymphohistiocytosis

Hemophagocytic lymphohistiocytosis(HLH)is a highly fatal condition with the positive feedback loop between continued immune cell activation and cytokine storm as the core mechanism to mediate multiple organ dysfunction.Inspired by macrophage membranes harbor the receptors with special high affinity for proin-flammation cytokines,lipopolysaccharide(LPS)-stimulated macrophage membrane-coated nanoparticles(LMNP)were developed to show strong sponge ability to both IFN-γand IL-6 and suppressed overactivation of macrophages by inhibiting JAK/STAT signaling pathway both in vitro and in vivo.Besides,LMNP also efficiently alleviated HLH-related symptoms including cytopenia,hepatosplenomegaly and hepatorenal dysfunction and save the life of mouse models.Furthermore,its sponge effect also worked well for five human HLH samples in vitro.Altogether,it’s firstly demonstrated that biocompatible LMNP could dampen HLH with high potential for clinical transformation,which also provided alternative insights for the treatment of other cytokine storm-mediated pathologic conditions such as COVID-19 infection and cytokine releasing syndrome during CAR-T therapy.

Synthesis and Characterization of SiO_2 Coated γ-Fe_2O_3 Nanocomposite Powder for Hyperthermic Application

SiO2 coated γ-Fe2O3 nanocomposite powder has been successfully synthesized by chemical vapor condensation process and its feasibility on hyperthermic application was investigated in this study. The power loss of SiO2 coated γ-Fe2O3 nanocomposite powder which means the magnetic heating effect under alternative magnetic field was much higher than the single phase γ-Fe2O3 nano powder due to the very fine size under 20 nm and well dispersion in biologically compatible SiO2 matrix. The superparamagnetism and hyperthermic property of SiO2 coated γ-Fe2O3 nanocomposite powder were discussed in terms of microstructural development in this study.

Scalable gas-phase processes to create nanostructured particles

The properties of nanoparticles are often different from those of larger grains of the same solid material because of their very large specific surface area. This enables many novel applications, but properties such as agglomeration can also hinder their potential use. By creating nanostructured particles one can take optimum benefit from the desired properties while minimizing the adverse effects. We aim at developing high-precision routes for scalable production of nanostructured particles. Two gas-phase synthesis routes are explored. The first one - covering nanoparticles with a continuous layer - is carried out using atomic layer deposition in a fluidized bed. Through fluidization, the full surface area of the nanoparticles becomes available. With this process, particles can be coated with an ultra-thin film of constant and well-tunable thickness. For the second route - attaching nanoparticles to larger particles - a novel approach using electrostatic forces is demonstrated. The micron-sized particles are charged with one polarity using tribocharging. Using electrospraying, a spray of charged nanoparticles with opposite polarity is generated. Their charge prevents agglomeration, while it enhances efficient deposition at the surface of the host particle. While the proposed processes offer good potential for scale-up, further work is needed to realize large-scale processes.

SiO2-coated pure anatase TiO2 catalysts for enhanced photo-oxidation of naphthalene and anthracene

Our current efforts reveal the preparation of SiO2@TiO2 nanocomposites having different thicknesses of silica shell and the relationship to photocatalytic activity （PCA） for the photo-oxidation of naph-thalene and anthracene. The presence of SiO2 coating over TiO2 surface was demonstrated by FT-IR analysis, with peaks corresponding to Si-O-Si （1081 cm 1） and Si-O-Ti （950 cm-1） bonds observed. High-resolution transmission electron microscopy analysis confirmed the presence of SiO2 in the as- prepared nanocomposites and the amount of Si, Ti, and O was determined by energy dispersive X-ray spectroscopy analysis. Increasing the Si02 shell thickness increases the surface area of the nanocompos- ites （69-235 m2/g）, which enhances naphthalene/anthracene adsorption. However, the observed PCA trend presents an inverse correlation to the adsorption studies, where the as-prepared samples possess- ing the highest surface areas exhibited the least PCA, while catalysts having lower surface areas （among silica coated samples） displayed the highest PCA in the degradation of naphthalene and anthracene to CO2. Despite complete degradation of naphthalene and anthracene, incomplete mineralization occurred, ascribed to the formation of various intermediates, identified by GC-MS analysis.