A novel low-clay translucent whiteware based on anorthite

This study was carried out to characterize the properties of a novel low-clay translucent whiteware suitable for daily use. The low-clay whiteware is produced from coarsely and finely milled prefired materials of the same composition plus a small amount of clay. It consists of anorthite (CaO·Al₂O₃·2SiO₂) and mullite (3Al₂O₃·2SiO₂) crystalline phases and a glassy phase with high crystalline to glassy phase ratio. The development of needle shaped long mullite crystals that were forming three dimensional interlocking network had significant effect on the elimination of pyroplastic deformation during glaze firing. Typical flexural strength and fracture toughness values were ∼110 MPa and ∼1.85 MPam^1/2, respectively. The low-clay whiteware had relatively low (4.6 × 10⁻⁶/°C) thermal expansion coefficient which made possible to glaze the whiteware with a typical hard porcelain glaze. A continuous interface layer was produced between the whiteware and the glaze and no crack was present through layer because of expansion mismatch.     

Spectrophotometric and electrochemical behavior of a novel azocalix[4]arene derivative as a highly selective chromogenic chemosensor for Cr

In this study, a novel azocalix[4]arene derivative, 5,11,17-tris[(1-naphtyl)azo]-25,26,27,28-tetrahydroxy-calix[4]arene (NAC4) bearing napthyl groups on the upper rim was synthesized. Its complexation behavior for alkali, alkaline-earth and various heavy metal ions (Li⁺, Na⁺, K⁺, Rb⁺, Cs⁺, Mg²⁺, Ca²⁺, Sr²⁺, Ba²⁺, Pb²⁺, Hg²⁺, Ni²⁺, Cd²⁺, Cu²⁺, Zn²⁺, Co²⁺, Fe²⁺, Cr³⁺, Ag⁺) was investigated by spectroscopic and voltammetric methods. This chemosensor exhibits decreased absorbance in the presence of Hg²⁺ and a unique absorbance quenching effect only for Cr³⁺. In addition, a new absorption band centered at 565 nm with the formation of the 1:1 host–guest complex (Cr³⁺-NAC4) was observed in the case of Cr³⁺, leading to an obvious color change from light orange to dark lilac. In voltammetric experiments, Cr³⁺ ions decreased voltammetric peaks of NAC4, whereas no significant changes occurred in the presence of the other metal ions. The Benesi–Hildebrand method was used to determine a logarithmic value of 3.76 for the association constant of the complex between Cr³⁺ and NAC4.     

A new photopolymerization system for vinyl monomers

A mixture of Ce⁺³ salt and an aminomethylene phosphonic acid, such as amino tri(methylene phosphonic acid) (ATMP), diethylene triamine penta(methylene phosphonic acid), N,N‐di(methylene phosphonic acid) ethanol amine, N,N‐di(methylene phosphonic acid)‐N‐methylamine, N‐oxo‐N,N,N‐tri(methylene phosphonic acid), or 1‐hydroxy‐ethylidene‐1,1‐diphosphonic acid, was used for the photopolymerization of acrylonitrile, vinyl acetate, acrylic acid, and styrene in water. Molecular weights of the polymers decreased with increasing concentration of both Ce⁺³ salt and ATMP. The effect of oxygen, light, pH, and the addition order on polymerization were also studied. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2494–2499, 2002     

Synthesis and Self-assembling Properties of 2,2′:6′,2″-Terpyridine-Based Carbon Nanotube Coordination Polymers

A novel metallo-supramolecular polytopic ligand was synthesized from the attachment reaction involving an amino group-functionalized multi-wall carbon nanotube and 4-chloro-2,2′:6′,2″-terpyridine used for the preparation of metallo-supramolecular polymers with Co(II) or Ni(II) ions. Different colors were observed depending on either the ligands or the metal ions in this type of supramolecular assembly. The created supramolecular polymers were characterized by means of structure, morphology, and stimuli-responsive performance employing scanning electron microscopy, amperometric techniques, UV–Vis and Fourier transform infrared spectroscopy. UV–Vis spectroscopy and cyclic voltammetry studies confirmed that both the optical and electrochemical properties of metallo-supramolecular materials are affected by the substituent at the pyridine periphery.     

Effects of preform deformation behavior on the properties of the poly(ethylene terephthalate) bottles

Plastics bottles made out of poly(ethylene terephthalate) (PET) are usually produced by injection stretch blow molding. Optimization of the process parameters is necessary to achieve bottles with adequate top load and burst strength. However, doing so experimentally is time‐consuming and costly. To overcome this difficulty, simulation packages based on finite element analysis methods have been developed. In this study, process optimization of a 350‐mL PET fruit juice bottle was carried out by means of BlowView and ANSYS simulation packages. BlowView was used for the ISBM process simulation and ANSYS for structural analysis of the bottles. The bottles were produced under different process conditions where the timing of the stretch rod movement was varied in relation to the activation of the blow pressure. The simulation results obtained through the both simulation packages were compared with experimental results. It was found that bottles of highest quality were produced if the sequencing of axial stretching and radial inflation results in simultaneous biaxial deformation of the preform. Truly biaxial orientation of PET molecules improved both top‐load and burst resistances of the bottles. The structural simulation studies performed by the ANYSYS simulation package validated most of our experimental findings. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Polymerization of epoxides catalyzed by a mixed‐valent iron trifluoroacetate [Fe3O(O2CCF3)6(H2O)3]

The readily available mixed‐valent iron trifluoroacetate complex [Fe₂^IIIFe^II(µ₃‐O)(O₂CCF₃)₆(H₂O)₃] is an effective catalyst for the polymerization of epoxides. A very small amount of the catalyst (1.0–0.01 mol%) could initiate the polymerization of cyclohexene oxide, cyclopentene oxide and epichlorohydrin. Based on quantitative end‐group analysis by ¹⁹F NMR spectroscopy, a Lewis acid (LA^⊕) catalyzed anionic reaction mechanism is proposed. Copyright © 2012 Society of Chemical Industry     

Influence of Plasma Spray Parameters on Formation and Morphology of ZrO2–8 wt% Y2O3 Deposits

Spray prints of thermal spray coatings were created on glass slides for air-plasma-sprayed 8-wt%-yttria-partially-stabilized zirconia (YSZ) deposits. The spray parameters such as carrier gas flow rate, standoff distance, and torch power were systematically changed to investigate the influence of these parameters on the YSZ deposit characteristics. The deposit properties such as deposition efficiency (DE), substrate coverage, deposit thickness, and roughness were measured. The deposits sprayed with a 3.5–4.0 L/min carrier gas flow rate at an 80 mm standoff distance exhibited higher values of DE within the range of studied process parameters. The DE increased as much as 25% by varying the carrier gas flow rate from 2.0 to 4.0 L/min. The deposits sprayed at a higher standoff distance and low torch power gave poor deposit characteristics. The deposit characteristics were compared with the in-flight particle parameters and revealed that the deposit characteristics strongly depended on the in-flight particle temperature. Using the in-flight particle properties, the flattening ratio and the splat thickness were calculated. The average size of particles adhering to the substrate was found to drastically change with a change of process conditions, being much less than the average size of the starting powder.     

Free radical crosslinking of unsaturated bacterial polyesters obtained from soybean oily acids

Summary Poly(-3-hydroxy alkanoate) containing unsaturated side chains, PHA-soybean, were produced by feeding Pseudomonas oleovorans with soybean oily acids obtained from soybean oil. Unsaturation of PHA-soybean were found to be 10 mol-% of unsaturated side chains. Main saturated part of the biopolymer was Poly(3-hydroxy octanoate) with minor hexanoate and decanoate units. PHA films were crosslinked via free radical mechanism by means of thermally or under UV irradiation in the presence of benzoyl peroxide, benzophenon, and /or ethylene glycol dimethacrylate (EGDM). Crosslinking yield of the PHA films were found to be from 81 to 93 wt.-% from the sol-gel analysis. Swelling properties of the crosslinked PHA films in chloroform and toluene were also studied. Mc values of crosslinked PHAs were also calculated using Flory-Rehner equation. The crosslinked biopolyester obtained by thermally at 60 °C with benzoyl peroxide indicated the highest crosslinking density. Glass transition temperatures (Tg) of crosslinked biopolyester samples were changed from −33 to −45 °C while that of PHA-soybean was −60 °C. Received: 16 June 2000/Revised version: 22 January 2001/Accepted: 20 May 2001     

Flexible poly(styrene-ethylene-butadiene-styrene) hybrid nanofibers for bioengineering and water filtration applications

Among the thermoplastic elastomers that play important roles in the polymer industry due to their superior properties, styrene-based species and polyurethane block copolymers are of great interest. Poly(styrene-ethylene-butadiene-styrene) (SEBS) as a triblock copolymer seems to have the potential to meet many demands in different applications due to various industrial requirements where durability, biocompatibility, breaking elongation, and interfacial adhesion are important. In this study, the SEBS triblock copolymer was functionalized with natural (Satureja hortensis, SH) and synthetic (nanopowder, TiO₂) agents to obtain composite nanofibers by electrospinning and electrospraying methods for use in biomedical and water filtration applications. The results were compared with thermoplastic polyurethane (TPU) composite nanofibers, which are commonly used in these fields. Here, functionalized SEBS nanofibers exhibited antibacterial effect while at the same time improving cell viability. In addition, because of successful water filtration by using the SEBS composite nanofibers, the material may have a good potential to be used comparably to TPU for the application.