Dispersion of carbon nanotubes in low pH aqueous solutions by means of alumina-coated silica nanoparticles

A novel noncovalent and inorganic method was used to disperse multiwalled carbon nanotubes (MWCNTs) in aqueous solutions through alumina-coated silica (ACS) nanoparticle halos. MWCNTs were directly dispersed into a highly charged ACS nanoparticle aqueous solution without functionalization of their surfaces. The dispersed MWCNTs were characterized by transmission electron microscopy and atomic force microscopy. Raman spectroscopy of MWCNTs prepared from dispersion in the ACS solution revealed reduced bundling compared to the corresponding untreated MWCNTs. The characteristic Raman peak at about 1570 cm⁻¹, corresponding to the G band, shifted to a higher wavenumber with a narrower peak. It was possible to disperse up to 20 mg/mL of MWCNTs in a 1 wt% ACS nanoparticle aqueous solution at pH 2. This homogeneous MWCNT-ACS aqueous solution was stable for weeks after ultrasonication.     

Synthesis of Ba(Mg1/3Ta2/3)O3 Microwave Ceramics through a Sol–Gel Route Using Acetate Salts

A sol–gel process to unsophisticatedly synthesize Ba(Mg_1/3Ta_2/3)O₃ (BMT) ceramics at low cost has been developed in the present work. This process involves the reaction of TaCl₅ with acetates of Ba and Mg in the presence of citric acid. Pure BMT polycrystalline powders can be obtained by calcining the synthesized products at 1000°C. The BMT powders were found to have a primary particle size as small as 100 nm. BMT ceramics with favorable structural characteristics can be obtained from sintering of the sol–gel BMT at temperatures much lower than that for the conventional solid-state BMT. Sintering the sol–gel BMT in pellet form at 1300°C resulted in an ordering parameter of 0.72 for the pellet, and a relative density of >95% was achieved with sintering at 1500°C. The grain size of the sintered sol–gel BMT was large and uniform in comparison with the products from the solid-state method. Using the sol–gel route, sintering at temperatures as low as 1400°C gave ceramics with acceptable microwave dielectric properties (a dielectric constant of 16 and Qf factor of 14 400 GHz), while higher temperatures (>1600°C) are needed for the solid-state route to give similar properties.     

GRAPHICAL SOLUTION OF MULTISTAGE FLUIDIZED BED HEAT EXCHANGER

The design of multistage fluidized beds for heat exchange necessitates the solution of the mass and energy balance equations combined with the equilibrium relations for each stage. This paper presents a novel way of applying well known methodology to a different technology, one where it has not been widely applied.

In the present work a McCabe-Thiele type of graphical approach is presented for both counter-current and cross-current contacting multiple fluidized beds. The necessary equations for a multistage calciner are developed and the application of the proposed method is demonstrated. Generalized fluidized bed efficiency for counter-current and cross-current multiple fluidized bed is presented.     

Effects of molecular weight and molecular structure of low profile additives on the properties of bulk molding compound (BMC)

The effects of molecular weight and molecular structure of styrene(St)‐based and vinyl acetate(VAc)‐based low‐profile additive (LPA) on the curing kinetics and compatibility of unsaturated polyester (UP)/LPA system and linear shrinkage, water absorption rate, surface gloss and pigmentability of bulk molding compound (BMC) were investigated. Results show that the curing reaction rate decreases with an increase of the molecular weight of LPA due to the chain entanglement effect. The plasticizing effect of LPA on the (UP) network was reduced with an increase of the molecular weight of LPA. Water absorption of BMC increases as the molecular weight of LPA increases, implying that more microvoids were formed inside the BMC, resulting a lower linear shrinkage rate, and worse pigmentability. However, good shrinkage control LPA does not necessarily lead to a smoother surface and better surface gloss. Furthermore, modified LPAs possess better compatibility with UP, the final curing conversion of UP is elevated, and both better shrinkage control and surface properties are also observed.     

Glass transition and exclusion model in crystallization of polyether-polyester block copolymers with amide linkages

Polyether-polyester block copolymers having various polyetheramide contents were synthesized. Single glass transition intermediated in temperature between the glass transition temperatures of polyester and polyetheramide components was found for all of polyether-polyesters. The compositional variation of glass transition exhibited a similar trend to the predicted result of thermodynamic theory for compatible polymer blends. The incompatible pair of homopolyester and homopolyether was forced to be compatible after copolymerization. A modified theoretical prediction for the glass transition of copolymers based on the thermodynamic theory is proposed. Consistent results between theoretical prediction and experimental measurements were found. Unlike homopolyesters, the glass transition temperature of copolymer amorphous domains gradually decreases with crystallization time. An exclusion model for the crystallization of polyester segments in copolymers is proposed. The temperature width of the glass transition increases with crystallization time. The broadening towards the low temperature side in glass transition is interpreted as the evidence of crystallization-induced partial phase separation. Instead of forming macroscopic segregation, the excluded polyether segments resided in-between crystalline polyester lamellae and mix with amorphous polyesters to generate amorphous domains exhibiting concentration gradient along the lamellar basal surface normal. Further increasing the polyetheramide segment content brings the excluded polyetheramide segments to form domains among the crystallized polyester spherulites so as to inhibit the occurrence of spherulitic impingement.     

Properties and pervaporation separation of hydroxyl‐terminated polybutadiene‐based polyurethane/poly(methyl metharcylate) interpenetrating networks membranes

Hydroxyl‐terminated polybutadiene (HTPB), 4,4′‐dicyclohexyl methane diiscyanate (H₁₂MDI), and 1,4‐butane diol are used to synthesize polyurethane (PU) solutions by two‐stage process. Interpenetrating networks (IPNs) of HTPB‐based PU and poly(methyl methacrylate) (PMMA) with HTPB/MMA (wt/wt % ratio) = 2.0, 1.5, 1.0, 1.5, 0.8, and 0.6, which are designated as IPN1 to IPN5, respectively, are synthesized by sequential polymerization technique. Thermal properties, tensile strength, and contact angle of membranes increase with the increase of MMA content, while the elongation of membranes show the reverse trend. Characterization of membranes are investigated by C?C/C?O absorption ratio and infrared absorption frequency shiftment. These PU and IPN membranes are used for the separation of ethanol/water and isopropanol/water solution by pervaporation test. IPN3 membrane possesses the largest pervaporation permeability and the separation factor. The pervaporation results of ethanol/water feed has the same trend as that of isopropyl alcohol (IPA)/water solution. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

An EGF-pseudomonas exotoxin A recombinant protein with a deletion in toxin binding domain specifically kills EGF receptor bearing cells

We constructed two chimeric toxins; one composed of epidermalgrowth factor (EGF) and pseudomonas exotoxin A (PE), designatedEGF-PE and the other composed of EGF and PE with a deletionof the Ia domain (cell-binding domain), designated EGF-PE (Ia).Both chimeric toxins reacted with anti-EGF and anti-PE antibodies.The cell-killing experiments showed that EGF-PE, but not EGF-PE(Ia),was cytotoxic to the murine fibroblast cell line NR6, whichcarried the PE receptor, but not the EGF receptor. However,after NR6 was transfected with DNA for the expression of humanEGF receptor, the transfected cell line, designated NRHER5,overexpressed human EGF receptors and became sensitive to EGF-PE(IA).The cytotoxicity of EGF-PE(Ia), but not EGF-PE, to NRHER5 canbe completely blocked by an excess amount of EGF. To completelyreverse the cytotoxicity of EGF-PE on NRHER5, both the EGF receptorpathway and the PE receptor pathway need to be blocked. Theseresults suggest that EGF-PE exhibits both EGF and PE bindingactivities, while EGF-PE(IA) possesses only EGF binding activity.Thus, EGF-PE(Ia) may be a better chimeric toxin than EGF-PEin terms of target specificity to EGF receptor bearing cells.We, therefore, examined the cytotoxicity of EGF-PE(Ia) to varioushuman cancer cell lines. We find that human cancer cells containingmore EGF receptors are more sensitive to EGF-PE(Ia).     

Inclusion of third-person perspective in CAVE-like immersive 3D virtual reality role-playing games for social reciprocity training of children with an autism spectrum disorder

Universal Access in the Information Society - The present study aimed to improve the ability of children with autism to recognize emotions correctly. We used our third-person perspective...     

High-efficiency ammonium polyphosphate intumescent encapsulated polypropylene flame retardant

The flame retardant polypropylene containing the micro-envelope core-shell structure flame retardant, which encapsulated ammonium polyphosphate into melamine-formaldehyde resin and sodium silicate through in situ polymerization was prepared with polyamide 6, added as a carbon-forming agent. The composition of ammonium polyphosphate, encapsulated ammonium polyphosphate with melamine-formaldehyde resin and the micro-envelope core-shell structure flame retardant were characterized. The fire safety and thermal stability were investigated and showed an improvement including limiting oxygen index, thermogravimetric analysis, vertical burning tests, and microscale combustion calorimeter. The burned compounds were also studied to confirm the burning mechanism. The results showed the flame retardant performance had been greatly improved, while polyamide 6 had better char-forming effect. Besides, the water solubility of flame retardants and their influence on the mechanical properties of polypropylene were also investigated. The results on the effects of additives demonstrated a high efficiency flame retardant to polypropylene. A core-shell flame retardant that sodium silicate and melamine-formaldehyde resin-coated ammonium polyphosphate had been constructed. The effect of the built flame retardant system on the combustion performance of polypropylene was studied from the mechanism and performance. The LOI of the most flame retardant polypropylene reached 28.6%, and UL-94 reached the V-0 level.     

Determination of the long term corrosion behavior of coated steel with A.C. impedance measurements

A previous study of the a.c. impedance of thin polymer films on aluminum alloys, steel, and phosphated steel, determined over a wide frequency range, has resulted in a general model for the electrochemical impedance across the coated surfaces. According to this model, penetration of the coating by the electrolyte results in an impedance behavior which is typical of a dielectric film short-circuited by conducting electrolytic paths perpendicular and parallel to the polymer/metal interface. Comparison of the time dependence of the impedance of coated steel substrates with the impedance across a free film has demonstrated that the corrosion of the substrate enhances the development of parallel paths of ionic conduction in the coating. A.c. impedance measurements carried out on polybutadiene-coated steels pretreated by different procedures determine quantitatively the resistance R_p of the conducting paths. The time dependence of R_p for the coated substrates has been determined for exposure periods of up to three weeks. Visual observation of the corroded and delaminated areas according to ASTM D610 has been carried out simultaneously, and correlations have been established with R_p. The results are discussed in terms of the possibility to predict the corrosion behavior of a coated metal, based on the measurement of R_p.