Improving the Performance of Poly(caprolactone)-Cellulose Acetate-Tannic Acid Tubular Scaffolds by Mussel-Inspired Coating.

Small-diameter artificial blood vessels are increasingly being used in clinical practice. However, these vessels are prone to thrombus, and it is necessary to improve blood compatibility. Surface coating is one of the commonly used methods in this regard. Inspired by the biomimicry of mussels, the use of deposition technology to obtain coating coverage on the surface of fibers has significantly piqued the interest of researchers recently. In this study, tubular scaffolds consisting of a composite of poly(caprolactone), cellulose acetate, and tannic acid (TA) were electrospun, and then the scaffolds were treated with different Fe(III) solutions (iron(III) chloride hexahydrate (FeCl3'6H2O)) to obtain four tubular scaffolds: F0, F5, F15, and F45. According to scanning electron microscopy (SEM) and field emission-SEM results, TA/Fe(III) complex is coated on the fiber of the scaffold after post-treatment; the fiber surface morphology changes with different Fe(III) concentrations. This provides designability to the performance of tubular scaffolds. The tensile strength of the F5 tubular scaffold (3.33 MPa) is higher than that of F45 (3.14 MPa), while the strain (83.9%) of the F45 tubular stent was 2.26 times that of the F5 (37.2%). In addition, cytotoxicity and antithrombotic performance were evaluated. The test results show that surface TA/Fe(III) coating treatment can affect the cytotoxicity and anticoagulation performance of the scaffold surface. The biomimetic TA/Fe(III) coating of mussels used in this study improves the performance of artificial blood vessels.

Effect of surface structure on the antithrombogenicity performance of poly(-caprolactone)-cellulose acetate small-diameter tubular scaffolds.

Small-diameter artificial blood vessels have always faced the problem of thrombosis. In this research, three types of poly(-caprolactone)-cellulose acetate (PCL-CA) composite nanofiber membranes were prepared by various collectors to make into a tubular scaffold with a 4.5-mm diameter. The collector consisted of two sizes of stainless steel wire mesh large-mesh (LM) and small-mesh (SM), respectively. There is also a random flat (RF) that acts as the third type collector. The nanofiber membrane's surface structure mimicked the collectors' surface morphology, they named LM, SM and RF scaffolds. The water contact angles of RF and LM scaffolds are 126.5° and 105.5°, and the distinct square-groove construction greatly improves the contact angle of LM. The tubular scaffolds' radial mechanical property test demonstrated that the large-mesh (LM) tubular scaffold enhanced the strain and tensile strength; the tensile strength and strain are 30 % and 148 % higher than that of the random-flat (RF) tubular scaffold, respectively. The suture retention strength value of the LM tubular scaffold was 103 % higher than that of the RF tubular scaffold. The cytotoxicity and antithrombogenicity performance were also evaluated, the LM tubular scaffold has 88 % cell viability, and the 5-min blood coagulation index (BCI) value was 89 %, which is much higher than other tubular scaffolds. The findings indicate that changing the tubular scaffold's surface morphology cannot only enhance the mechanical and hydrophilic properties but also increase cell survival and antithrombogenicity performance. Thus, the development of a small-diameter artificial blood vessel will be a big step toward solving the problem on thrombosis. Furthermore, artificial blood vessel is expected to be a candidate material for biomedical applications.

Heat-Stimuli Shape Memory Effect of Poly (ε-Caprolactone)-Cellulose Acetate Composite Tubular Scaffolds.

Small-diameter artery disease is the most common clinical occurrence, necessitating the development of small-diameter artificial blood vessels. In this study, seven types of poly(-caprolactone)-cellulose acetate (PCL-CA) composite nanofiber membranes were prepared with different proportions of PCL and CA. The adhesion and growth of Mc3t3-e1 cells were considered to confirm the in vitro cytocompatibility of PCL-CA membranes. A smooth stainless-steel mandrel with a diameter of 4 mm was used to roll up the prepared nanofiber membranes to produce the tubular scaffold with 50 °C hot water. The tubular scaffolds were subjected to axial and circumferential tensile tests. The mechanical performance of the PCL-CA tubular scaffold could be improved by increasing the layers. In addition, the burst pressure (BP) of the tubular scaffolds was increased with the layers, and the BPs of six-layer (2380 ± 36.8 mmHg) and eight-layer (3720 ± 80.5 mmHg) tubular scaffolds were much higher than that of the human saphenous vein (2000 mmHg). The compression shape memory performances of the PCL-CA tubular scaffold with different layers were also investigated to simulate and analyze the contraction and expansion of tubular scaffolds. The experimental results showed that the compression strain of the tubular scaffold in the diameter direction reached 35%, and the ultimate shape recovery rate reached 87%. However, the shape fixity rate and shape recovery rate increased, demonstrating that the optimum number of layers can improve the compression shape memory performance of the tubular scaffold. The results of this study, including comprehensive morphological and mechanical properties and cytocompatibility, indicated the potential applicability of PCL-CA tubular scaffolds as tissue engineering grafts.

Actuation Characteristics and Mechanism of Electroactive Plasticized Thermoplastic Polyurethane.

As interesting alternatives, electroactive actuators based on plasticized thermoplastic polyurethane (TPU) have shown their potential in developing soft robotics due to the large bending deformation, fast response, and good durability, especially their designable properties. Understanding the actuation mechanism is essential for controlling soft actuators as well as developing novel ones. In this work, the behaviors of the plasticizer and TPU membranes in electric fields were investigated and observed in situ by a microscope, showing that the plasticizer molecules migrated toward the anode of the actuator. It is found that there was a very thin plasticizer-rich layer formed in the material because of the accumulation of negatively charged plasticizer molecules, basing on the results of electrochemical impedance measurement and space charge measurement. This further led to a lower Young's modulus but an internal electric field with a higher density in this layer, resulting in the deformation of the actuator. Furthermore, based on the actuation mechanism, some actuation characteristics of the developed soft actuators were clarified. The maximum deflection of these actuators increased with the number of cycle tests, and in each cycle test, the deflection quickly reached the maximum value and then gradually decreased. It is believed that these characteristics are strongly related to the behaviors of plasticizer molecules, which were investigated accordingly.

Cellulose acetate/multi-wall carbon nanotube/Ag nanofiber composite for antibacterial applications.

Herein we propose cellulose acetate/carbon nanotube/silver nanoparticles (CA/CNT/Ag) nanofiber composite for antibacterial applications. The nanofiber composite are expected to avoid harmful effects of silver (i.e. argyria and argyrosis) owing to anchoring of silver nanoparticles on carbon nanotubes (CNTs) and embedding of the composite inside cellulose acetate (CA) matrix. The carbon nanotubes/silver nanoparticles (CNT/Ag) nanocomposite localized inside the CA polymer matrix allow minimal/no direct contact of silver nanoparticles with human cells and are expected to show reduced silver leaching. The cellulose acetate (CA) nanofibers loaded with silver nanoparticles anchored multiwall carbon nanotubes (CNT/Ag) were fabricated by electrospinning. The samples were studied with scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), Fourier transform infra-red spectroscopy (FTIR), tensile strength tests and antibacterial assays. Synthesis of the CNT/Ag nanocomposite was confirmed with XPS, XRD, EDS and TEM analysis. SEM images showed regular morphology of the CA/CNT/Ag nanofiber composites. TEM images depicted anchoring of silver nanoparticles on CNTs and embedding of CNT/Ag in the CA nanofiber matrix. The antibacterial test results demonstrated excellent antibacterial performance of the CA/CNT/Ag. The CA/CNT/Ag samples ensured effective bacterial growth inhibition on agar plates, in liquid medium (optical density, OD590nm) (for 48 h) and in bactericidal assay (relative cell viability, %). Our results suggested CA/CNT/Ag composite nanofibers as potential candidate for safer antibacterial applications.

Electromagnetic Wave Absorption Performance of Carbonized Rice Husk Obtained at Various Temperatures.

Agricultural wastes such as rice husks (RHs) are valuable due to their feasibility to be converted into carbon materials, low cost, and abundancy in contrast to the conventional carbon material sources. In this study, RHs are carbonized at various temperatures from low to high temperatures, and their electromagnetic (EM) wave absorption properties are evaluated. Carbon materials, silicon carbide (SiC) whiskers, and SiC particles are obtained from RHs carbonized at 1500 °C (CRH1500) for 0.5 h with presence of Ar gas at 1 atm. In order to evaluate their EM wave absorption performance, complex permittivity and permeability are measured by using vector network analyzer, and the values are utilized in the reflection loss (R.L.) calculation according to the transmission line theory. CRH1500, 40 wt% with thickness of 1.6 mm exhibits minimum R.L. of ≈-55.4 dB (>99.9997% absorption) at 11.37 GHz and response bandwidth (R.L. < 10 dB, > 90% absorption) of 4.21 GHz. Low-cost and abundant RHs, carbonized at various temperatures, show significant absorption performance. Their absorption performance and response bandwidth are highly dependent on matching thickness, indicating that they can be easily modulated for promising electromagnetic wave absorber materials.

Characterizations and application of CA/ZnO/AgNP composite nanofibers for sustained antibacterial properties.

Although silver based nanofibers possess excellent bactericidal and bacteriostatic characteristics. However, excess release/contact with silver may induce harmful side-effects including carcinoma, argyria, argyrosis and allergies. Similarly, silver depletion may limit prolonged antibacterial activities as well. Thus present research proposes electrospun CA/ZnO/AgNPs composite nanofibers for biologically safer and sustained antibacterial applications. The ZnO/AgNPs were synthesized using dopamine hydrochloride (Dopa) as reducing agent to immobilize AgNPs on ZnO nanoparticles. A simple solution-mixing procedure effectively generated AgNPs on ZnO nanoparticles. Strong adhesive characteristics of Dopa initiate adsorption of silver ions on ZnO nanoparticle surfaces and its metal ion reducing properties generate AgNPs. Additionally, the Dopa mediation generates strongly adhered AgNPs. The ZnO/AgNPs were used to fabricate CA/ZnO/AgNPs nanofibers. Characterization techniques, XRD, XPS, TEM, FTIR and SEM confirmed synthesis of nanocomposites. Crystallite sizes of ZnO and AgNPs calculated by Debye-Scherrer equation were 17.85 nm and 11.68 nm respectively. Antibacterial assays confirmed CA/ZnO/AgNP's effectiveness in growth inhibition of E. coli and S. aureus strains on agar plate and in liquid medium. The nanofiber composites demonstrated 100% bactericidal properties against both the test strains. Bacterial growth inhibition in LB medium for 108 h indicated suitability of CA/ZnO/AgNPs composite nanofibers in sustained antibacterial applications such as antibacterial wound dressings and other applications demanding sustained antimicrobial properties.

A comparative study on synthesis of AgNPs on cellulose nanofibers by thermal treatment and DMF for antibacterial activities.

Herein we present our research on generation of silver nanoparticles (AgNPs) on cellulose nanofibers by thermal treatment and DMF as reducing agents. The cellulose (CE) nanofibers were prepared by deacetylation of electrospun cellulose acetate (CA) nanofibers which were subsequently silver coated using AgNO3 followed by thermal and DMF induced reduction processes. The samples were characterized with scanning electron microscopy (SEM), Fourier transform infra-red spectroscopy (FTIR), X-ray diffraction spectroscopy (XRD), energy dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and antibacterial assays. Effect of these methods on mechanical properties, thermal stabilities (DTA analysis) and swelling of the CE nanofibers were also studied. Both the processes were effective and efficient in generation of AgNPs on CE nanofibers with higher contents and very good spatial distributions. The XRD, XPS and TEM results evidenced formation metallic AgNPs. TEM images depicted the CE nanofibers highly decorated with spherical AgNPs. The DMF induced process generated AgNPs with comparatively larger sizes. The antibacterial results confirmed excellent antibacterial performance of the CEAgNPs against S. aureus and E. coli. The CEAgNP nanofibers well decorated with AgNPs having good spatial distribution and excellent antibacterial performance suggests CEAgNPs as promising candidate for efficient antimicrobial activities.

Cellulose acetate nanofibers embedded with AgNPs anchored TiO2 nanoparticles for long term excellent antibacterial applications.

Silver nanoparticles (AgNPs) are effective antimicrobial agents however excess release of silver causes argyria and argyrosis. An strategy to avoid these detrimental side effects is immobilization of AgNPs on several organic and inorganic substrates. Herein, we propose immobilization of AgNPs on TiO2 nanoparticles by an environmentally green process subsequently incorporating the TiO2/AgNP into cellulose acetate (CA) nanofiber matrix. The TiO2/AgNP nanocomposite particles were prepared by coating TiO2 nanoparticles with polydopamine hydrochloride followed by a treatment in AgNO3 solution. Subsequently, the TiO2/AgNP nanocomposites were added into CA solution and electrospun to fabricate CA/TiO2/AgNP composite nanofibers. The samples were characterized by XRD, TEM, XPS, SEM, EDX, FTIR and antibacterial assays. Synthesis of TiO2/AgNP and its loading into CA nanofibers was confirmed by XRD, XPS, TEM and EDX analysis. SEM images indicated regular morphology of the nanofibers. The antibacterial test results confirmed CA/TiO2/AgNP composite nanofibers having excellent antibacterial performances for 36 h and substantial bacterial growth inhibition for 72 h.

Fabrication of gradient vapor grown carbon fiber based polyurethane foam for shape memory driven microwave shielding.

Gradient vapor grown carbon fiber (VGCF) based shape memory polyurethane foam (VGCF@SMPUF) was fabricated by alternate dipping in a gradually diluted VGCF@SMPU/DMF solution and distilled water for shape memory driven microwave shielding. Shape memory performance for this VGCF@SMPUF was achieved by heat transfer of thermally conductive VGCF. Shielding effectiveness (SE) was adjusted through different degrees of angle recovery. A consistent shielding effect from either side indicated that electromagnetic reflection may take place at both the surface and inside of the non-homogeneous composite shield. For shape memory effect, hot compression made this VGCF@SMPUF achieve a faster recovery time and higher recovery ratio owing to improved thermal conductivity. Moreover, VGCF@SMPUF, which was bent to the positive side (PS) with a higher VGCF content, showed shorter recovery time and higher recovery ratio than that bent to the negative side (NS) with a lower VGCF content. We attribute this result to the relatively small mechanical compression strength of the negative side with the lower VGCF content at the bending point when expanding from the positive side. Furthermore, hot compression obviously improved the shielding effectiveness of the VGCF@SMPUF, mainly through a considerable increase of the electrical conductivity. The VGCF@SMPUF hot compressed to a thickness of 0.11 mm achieved a SE value of ∼30 dB, corresponding to a shielding efficiency of ∼99.9%.

Sonication induced effective approach for coloration of compact polyacrylonitrile (PAN) nanofibers.

We present our research on dyeability of polyacrylonitrile (PAN) nanofibers following ultrasonic dyeing method. Although PAN has been extensively utilized in textile apparel, sportswear, upholstery and home furnishing, however, coloration of PAN nanofibers has not yet been reported. PAN is a compact fiber while the nanofiber structure makes it more difficult to color PAN nanofibers. PAN is generally dyed with basic dyes and dyeing is carried out in acidic conditions, while the dyeing process takes about two hours at boiling temperature. A systematic study on dyeability of PAN nanofibers will extend its use in textile apparel industry. Thus, we used ultrasonic energy and first time conducted our research on dyeability of electrospun PAN nanofibers using disperse dyes. Dyeing process parameters such as dyeing time, temperatures and concentrations of dyes were optimized. Ultrasonic dyeing of PAN nanofibers was compared with its conventional dyeing as well. Affect of ultrasonic dyeing on the morphology, chemical state, crystallographic structure and mechanical strength of PAN nanofibers has been studied. PAN nanofiber samples were characterized by SEM, FTIR, XRD and tensile strength tests. The results revealed 80 °C and 60 min as optimum temperature and time for ultrasonic dyeing of PAN nanofibers. The ultrasonic dyeing does not affect morphology, chemical and crystalline structure of the PAN nanofibers while it improves their mechanical strength. Our research suggests dyeability of PAN nanofibers with disperse dyes by ultrasonic method and their subsequent use in textile apparels.

Drug carrier three-layer nanofibrous tube for vascular graft engineering.

Currently available synthetic grafts demonstrate moderate success at the macrovascular level, but there are still challenges at small vascular scale (inner diameter of less than 6 mm). In this paper, silk fibroin (SF)/polyurethane (PU)/SF three-layer drug carrier nanofibrous tubes were developed for blood vessel repair with several advantages over existing designs. Our design consisted of a bionic three-layer microtube that was synthesized from the drug carrier SF and oligomeric proanthocyanidin nanofibers as the inner layer, PU nanofibers as the middle layer, and SF nanofibers as the outer layer. The results suggested that these three-layer tubes are attractive biocompatible materials for use as vascular grafts.

The effect of hydroxyapatite nanoparticles on mechanical behavior and biological performance of porous shape memory polyurethane scaffolds.

The scaffold which provides space for cell growth, proliferation, and differentiation, is a key factor in bone tissue engineering. However, improvements in scaffold design are needed to precisely match the irregular boundaries of bone defects as well as facilitate clinical application. In this study, controllable three-dimensional (3D) porous shape memory polyurethane/nano-hydroxyapatite (SMPU/nHAP) composite scaffold was successfully fabricated for bone defect reparation. Detailed studies were performed to evaluate its structure, apparent density, porosity, and mechanical properties, emphasizing the contribution of nHAP particles on shape recovery behaviors and biological performance in vitro. The effect of nHAP particles in porous SMPU/nHAP composite scaffold was found to enhance the compression resistance by 37%, shorten the compression recovery time by 41%, reduce the tensile resistance by 78%, reach the shape recovery ratio of 99%, and promote the cell proliferation by 13% after 7 days of culture. These results revealed that the 3D structure and aperture of as-prepared scaffold were controllable. And in minimally invasive surgery and bone repair surgery, this porous composite scaffold could significantly reduce the operative time and promote the bone cell growth. Therefore, this porous SMPU/nHAP composite scaffold design has potential applications for the bone tissue engineering. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 244-254, 2018.

From Cellulose Nanospheres, Nanorods to Nanofibers: Various Aspect Ratio Induced Nucleation/Reinforcing Effects on Polylactic Acid for Robust-Barrier Food Packaging.

The traditional approach toward improving the crystallization rate as well as the mechanical and barrier properties of poly(lactic acid) (PLA) is the incorporation of nanocelluloses (NCs). Unfortunately, little study has been focused on the influence of the differences in NC morphology and dimensions on the PLA property enhancement. Here, by HCOOH/HCl hydrolysis of lyocell fibers, microcrystalline cellulose (MCC), and ginger fibers, we unveil the preparation of cellulose nanospheres (CNS), rod-like cellulose nanocrystals (CNC), and cellulose nanofibers (CNF) with different aspect ratios, respectively. All the NC surfaces were chemically modified by Fischer esterification with hydrophobic formate groups to improve the NC dispersion in the PLA matrix. This study systematically compared CNS, CNC, and CNF as reinforcing agents to induce different kinds of heterogeneous nucleation and reinforce the effects on the properties of PLA. The incorporation of three NCs can greatly improve the PLA crystallization ability, thermal stability, and mechanical strength of nanocomposites. At the same NC loading level, the PLA/CNS showed the highest crystallinity (19.8 ± 0.4%) with a smaller spherulite size (33 ± 1.5 µm), indicating that CNS, with its high specific surface area, can induce a stronger heterogeneous nucleation effect on the PLA crystallization than CNC or CNF. Instead, compared to PLA, the PLA/CNF nanocomposites gave the largest Young's modulus increase of 350 %, due to the larger aspect ratio/rigidity of CNF and their interlocking or percolation network caused by filler-matrix interfacial bonds. Furthermore, taking these factors of hydrogen bonding interaction, increased crystallinity, and interfacial tortuosity into account, the PLA/CNC nanocomposite films showed the best barrier property against water vapor and lowest migration levels in two liquid food simulates (well below 60 mg kg-1 for required overall migration in packaging) than CNS- and CNF-based films. This comparative study was very beneficial for selecting reasonable nanocelluloses as nucleation/reinforcing agents in robust-barrier packaging biomaterials with outstanding mechanical and thermal performance.

In vitro degradation and possible hydrolytic mechanism of PHBV nanocomposites by incorporating cellulose nanocrystal-ZnO nanohybrids.

Fabrication and characterization of bbiodegradable nanocomposites based on poly (3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) matrix reinforced with cellulose nanocrystal (CNC)-ZnO nanohybrids via simple solution casting for possible use as antibacterial biomedical materials is reported. The obtained nanocomposites exhibited an excellent antibacterial ratio of 95.2-100% for both types of bacteria namely S. aureus and E. coli and showed 9-15% degradation after one week. The addition of CNC-ZnO showed a positive effect on hydrophilicity and barrier properties. More significantly, the nanocomposites with 10wt% CNC-ZnO showed enhancement in tensile strength (140.2%), Young's modulus (183.1%), and the maximum decomposition temperature (Tmax) value increased by 26.1°C. Moreover, this study has provided a possible mechanism for using such nanofillers on the hydrolytic degradation of PHBV, which was beneficial to obtain the high-performance nanocomposites with modulated degradation rate for antibacterial biomaterials.

Fabrication and characterization of shape memory polyurethane porous scaffold for bone tissue engineering.

Tissue engineering is a promising alternative for treating bone defects. However, improvements in scaffold design are needed to precisely match the irregular boundaries of bone defects as well as facilitate clinical application. In this study, a shape memory polyurethane scaffold was fabricated using a salt-leaching-phase inverse technique. Different sizes of salts were used to obtain scaffolds with different pore sizes. Scanning electron microscope, X-ray photoelectron spectroscopy, and X-ray micro-computed tomography analysis confirmed that three-dimensional porous polyurethane scaffolds were obtained. The mechanical properties and biocompatibility of the scaffolds were analyzed by compression testing, thermal mechanical analysis, and cell experiments with osteosarcoma MG-63 cells. The results revealed that the scaffolds had good mechanical properties and shape memory properties for bone repair, and also had the ability to promote cell proliferation. Thus, this scaffold design has good prospects for application to bone tissue engineering. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 1132-1137, 2017.

One-dimensional carbon nanotube@barium titanate@polyaniline multiheterostructures for microwave absorbing application.

Multiple-phase nanocomposites filled with carbon nanotubes (CNTs) have been developed for their significant potential in microwave attenuation. The introduction of other phases onto the CNTs to achieve CNT-based heterostructures has been proposed to obtain absorbing materials with enhanced microwave absorption properties and broadband frequency due to their different loss mechanisms. The existence of polyaniline (PANI) as a coating with controllable electrical conductivity can lead to well-matched impedance. In this work, a one-dimensional CNT@BaTiO3@PANI heterostructure composite was fabricated. The fabrication processes involved coating of an acid-modified CNT with BaTiO3 (CNT@BaTiO3) through a sol-gel technique followed by combustion and the formation of CNT@BaTiO3@PANI nanohybrids by in situ polymerization of an aniline monomer in the presence of CNT@BaTiO3, using ammonium persulfate as an oxidant and HCl as a dopant. The as-synthesized CNT@BaTiO3@PANI composites with heterostructures were confirmed by various morphological and structural characterization techniques, as well as conductivity and microwave absorption properties. The measured electromagnetic parameters showed that the CNT@BaTiO3@PANI composites exhibited excellent microwave absorption properties. The minimum reflection loss of the CNT@BaTiO3@PANI composites with 20 wt % loadings in paraffin wax reached -28.9 dB (approximately 99.87% absorption) at 10.7 GHz with a thickness of 3 mm, and a frequency bandwidth less than -20 dB was achieved from 10 to 15 GHz. This work demonstrated that the CNT@BaTiO3@PANI heterostructure composite can be potentially useful in electromagnetic stealth materials, sensors, and electronic devices.

Synthesis and microwave absorption properties of electromagnetic functionalized Fe3O4-polyaniline hollow sphere nanocomposites produced by electrostatic self-assembly.

Highly regulated Fe3O4-polyelectrolyte-modified polyaniline (Fe3O4-PE@PANI) hollow sphere nanocomposites were successfully synthesized using an electrostatic self-assembly approach. The morphology and structure of the Fe3O4-PE@PANI nanocomposites were characterized using field-emission scanning electron microscopy, transmission electron microscopy, Fourier-transform infrared spectroscopy, X-ray powder diffraction, thermogravimetric analysis, and X-ray photoelectron spectroscopy. The results showed that the as-prepared nanocomposites had well-defined sizes and shapes, and the average size is about 500 nm. The assembly process was investigated. Magnetization measurements showed that the saturation magnetization of the nanocomposites was 38.6 emu g-1. It was also found that the Fe3O4-PE@PANI nanocomposites exhibited excellent reflection loss abilities and wide response bandwidths compared with those of PANI hollow spheres in the range 0.5-15 GHz. The Fe3O4-PE@PANI nanocomposites are, therefore, promising for microwave absorption applications.

Facile synthesis of BaTiO3 nanotubes and their microwave absorption properties.

Uniform BaTiO(3) nanotubes were synthesized via a simple wet chemical route at low temperature (50 °C). The as-synthesized BaTiO(3) nanotubes were characterized using powder X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy. The results show that the BaTiO(3) nanotubes formed a cubic phase with an average diameter of ~10 nm and wall thickness of 3 nm at room temperature. The composition of the mixed solvent (ethanol and deionized water) was a key factor in the formation of these nanotubes; we discuss possible synthetic mechanisms. The microwave absorption properties of the BaTiO(3) nanotubes were studied at microwave frequencies between 0.5 and 15 GHz. The minimum reflection loss of the BaTiO(3) nanotubes/paraffin wax composite (BaTiO(3) nanotubes weight fraction = 70%) reached 21.8 dB (~99.99% absorption) at 15 GHz, and the frequency bandwidth less than -10 dB is from 13.3 to 15 GHz. The excellent absorption property of BaTiO(3) nanotubes at high frequency indicates that these nanotubes could be promising microwave-absorbing materials.

Buckling instability of circular double-layered graphene sheets.

In this paper, we study the buckling properties of circular double-layered graphene sheets (DLGSs), using plate theory. The two graphene layers are modeled as two individual sheets whose interactions are determined by the Lennard-Jones potential of the carbon-carbon bond. An analytical solution of coupled governing equations is proposed for predicting the buckling properties of circular DLGSs. Using the present theoretical approach, the influences of boundary conditions, plate sizes, and buckling-mode shapes on the buckling behaviors are investigated in detail. The buckling stability is significantly affected by the buckling-mode shapes. As a result of van der Waals interactions, the buckling stress of circular DLGSs is much larger for the anti-phase mode than for the in-phase mode.