Effect of Agglomeration on Mechanical Properties of Porous Zirconia Fabricated by Partial Sintering

Porous ZrO₂ ceramics were fabricated by compacting a fine ZrO₂ powder, followed by pressureless sintering. Two unidirectional pressures of 30 and 75 MPa were used to prepare the green compacts. The strength and the fracture toughness of porous ZrO₂ specimens sintered from the compacts prepared by 75 MPa were substantially higher than those by 30 MPa, especially for the specimens with low porosity. However, the corresponding Young's moduli were identical. This caused the strain to failure of these porous bodies to increase significantly with increasing compaction pressure. Microstructural analyses showed that a number of voids and small flaws existed in the green compacts prepared by the lower pressure, due to the agglomeration of fine ZrO₂ grains. It was revealed that the ZrO₂ agglomeration resulted in a localized nonuniform shrinkage and degraded the mechanical properties of porous ZrO₂ ceramics.     

Synthesis,characterization, and thermal properties of alternate copolymers containing N,N′‐bis(diphenylsilyl)tetraphenylcyclodisilazane

Hexamethyldisilazane was used as the starting material to synthesize N,N′‐bis(hydroxydiphenylsilanyl)tetraphenylcyclodisilazane (BHPTPC). By condensation polymerization of BHPTPC with α,ω‐bis(dialkylamino)dimethylsiloxane, a series of alternate copolymers containing N,N′‐bis(diphenylsilyl)tetraphenylcyclodisilazane was synthesized. GPC studies show that the highest molecular weight was obtained at a ratio of 1.005 : 1 (BHPTPC: α,ω‐bis(dimethyl amino)dimethylsiloxane). Data of DSC indicate that the temperature of glass transition (T_g) and temperature of melting point (T_m) decreased with the increasing of dimethylsiloxane segments units. Three stages of degradation were found in the thermogravimetric analysis curves. The activation energy of the copolymer (with m = 2, 3, and 7) was calculated by using Flynn–Wall–Ozawa method. The activation energy of the copolymer with m = 2, 3, and 7 at second stage is 214, 211, and 184 kJ/mol, respectively. Isothermal gravimetric analysis shows that for the same temperature and the same time, the weight loss of the alternate copolymer was greatly less than that of common polydimethylsiloxane. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 611–617, 2007     

Morphology and thermomechanical properties of recycled PET–organoclay nanocomposites

Recycled PET/organoclay nanocomposites were prepared by melt intercalation process with several amounts (1, 3, and 5 wt %) of clay modified with quaternary ammonium salt (DELLITE 67G) dispersed in a recycled poly(ethylene terephthalate) (rPET) matrix. The resultant mechanical properties (modulus and yield strength) of the nanocomposites were found to be different from those of rPET. Wide angle X‐ray scattering (WAXS) and Transmission Electron Microscopy (TEM) measurements have shown that although complete exfoliation was not achieved, delaminated clay platelets could be observed. Thermal analysis did not show significant changes in the thermal properties from those of recycled PET. Mechanical testing showed that nanocomposite properties were superior to the recycled PET in terms of strength and elasticity modulus. This improvement was attributed to nanoscale effects and strong interaction between the rPET matrix and the clay interface, as revealed by WAXS and TEM. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1839–1844, 2007     

Structure and properties of polyimide‐bonded magnets processed from prepolymers based on diacetyl derivatives of aromatic diamines and dianhydrides

We report a novel method of polyimide (PI) synthesis from prepolymers based on dianhydrides and diacetyl derivatives of aromatic diamines that facilitate the preparation of a melt processable mixture at 300 ± 10°C of the prepolymer and magnetic Nd‐Fe‐B alloy to provide PI‐bonded magnets with enhanced properties. It is shown that chemical structure of the prepolymers strongly influences viscosity behavior via crystallization of the oligoimide in the melt, leading to formation of PI with rigid‐rod like structure. This structural ordering of the prepolymers based on diacetyl derivative of diamine used in this study, if not controlled, leads to exponential increase of melt viscosity with time, making it practically impossible to prepare melt processable mixture of the magnetic particles and the PI prepolymers at elevated temperatures. The results obtained demonstrate that appropriate dianhydrides and diacetyl derivatives of diamines that do not lead to crystallization of oligoimides in prepolymer mixture can be used under controlled processing conditions to prepare melt‐processable PI‐bonded magnets containing rigid‐rod like PI structure that significantly increases thermal stability of the magnets. The temperature dependencies of the magnetic properties of the PI‐bonded magnets under conditions that they are likely to encounter during their service life were found to be remarkably similar to that of commercial thermoplastic magnets such as injection‐molded nylon magnets. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 478–485, 2006     

微波烧结Al2O3-TiC复合材料的研究

以纳米级TiC、Al2 O3 为原料 ,用微波烧结制备Al2 O3 -TiC复合材料 ,并与常规烧结比较。分析了两种烧结方法对制备试样的力学性能的影响 ,并探讨了添加剂对Al2 O3 -TiC复合材料烧结性能的影响     

Evaluation of Polyester Resin as a New Compatibilizer for SBR/PVC Blends

A polyester (PE) based on the glycolyzed products of PET was prepared and added in different concentrations to a series of SBR/PVC blends. The addition of the polyester showed that all properties of SBR/PVC blends were improved by incorporation of PE. Highest mechanical strength values were obtained at a polyester concentration of 7.5 phr. Thermal analysis as well as dynamic mechanical properties of SBR/PVC blends after the addition of 7.5 and 10 phr polyester indicated one single glass transition temperature. The dielectric losses (?") were analyzed in the frequency domains in the two terms of Fröhlich related to the Maxwell Wagner effect and the orientation of the aggregates caused by the movement of the main chain. The permittivity (?') values were found to increase by increasing the polyester content. This increase was followed by a decrease in the ?" up to a 7.5 phr polyester content after which no pronounced change was noticed.     

Fracture toughness of bisphenol A‐type epoxy resin

The relationship between the postcuring conditions and the fracture toughness of a bisphenol A‐type epoxy resin cured with acid anhydride was investigated. The glass transition temperature and fragility parameter, derived from the thermo‐viscoelasticity, were used to characterize the epoxy resin postcured under various conditions. Relationship between these two parameters and the fracture toughness was then investigated, based on the fractography results of a microscopic roughness examination of a fractured surface. The values of the glass transition temperature and fragility greatly depended on the postcuring conditions. The glass transition temperature was approximately 400 K when the crosslinking reaction was saturated. The fragility was independent of the saturation of the reaction and varied between 50 and 180. The results of the fracture test and fractography examination showed that there was no direct correlation between the glass transition temperature, the fracture toughness, and the roughness. On the other hand, there was a correlation between the fragility, fracture toughness, and roughness when the glass transition temperature saturated (at 400 K). As the fragility decreased from 180 to 50, the fracture toughness increased from 0.6 to 1.1 MPa · m^1/2 at the same glass transition temperature. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 10: 2266–2271, 2002     

Enhanced strain hardening in elongational viscosity for HDPE/crosslinked HDPE blend. I. Characteristics of crosslinked HDPE

Blending a crosslinked high‐density polyethylene (xHDPE) enhances melt strength and strain hardening behavior in elongational viscosity of high‐density polyethylene (HDPE) to a great degree. Gel fraction of xHDPE has a stronger effect on the strain hardening than sol fraction, although sol fraction also enhances the strain hardening to some degree. Further, the xHDPE crosslinked by peroxide in a compression mold exhibits more pronounced effect than xHDPE by radiation, which is attributed to the difference in the amount of the gel fraction. The xHDPE, which enhances the strain hardening, has sparse crosslink points in the network. Moreover, it was found from linear viscoelastic measurements, such as oscillatory modulus and relaxation modulus, that the xHDPE is characterized as a critical gel, which was also supported by the result of tensile testing. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 73–78, 2002     

Phosphorus Fractionation and Sorption in P-enriched Soils of Norway

Phosphorus (P) enrichment can lead to imbalance in nutrient availability and pollution of terrestrial and aquatic ecosystems. Hence studies were carried out to investigate fractionation and sorption of P in eleven P-enriched soils collected from different agro-climatic sites in Norway. Different P fractions viz. total, organic, inorganic (easily soluble P, Fe-P, Al-P, Ca-P and occluded P), P_w (water extractable), and NH₄-lactate extractable P (P_AL) at the beginning and after the completion of the experiments varied widely among the soils studied, indicating a wide variability of P supplying capacity of these soils. Soluble P was positively correlated to Ca-P (r = 0.94; P < 0.001), P_w (r = 0.87; P < 0.001), pH (r = 0.79; P < 0.01) and P_AL (r = 0.79; P < 0.01), whereas it was negatively correlated with ammonium oxalate-extractable Al (Al_ox) (r = ?0.68; P < 0.05). Iron-P was only moderately related to Al_ox(r = 0.64; P < 0.05) and P_ox(r = 0.70; P < 0.05), whereas it was not related to any of the other parameters tested. The α [α = P_ox/(Fe_ox + Al_ox)] was highly correlated with P_AL (r = 0.93; P < 0.001), pH (r = 0.87; P < 0.001), inorganic P (r = 0.80; P < 0.01) and P_w(r = 0.77; P < 0.01) but moderately to total P (r = 0.71; P < 0.05). Adsorption data fitted well to the Langmuir equation for most soils. The P affinity constant (k), adsorption maximum (b) and thus maximum buffering capacity (mbc) and adsorption isotherm of P were highest in the sandy clay soil from Øsaker, which also contained high amounts of Fe, Al and clay particles and the lowest in sandy soil from Vestrålen, which contained very high initial P_ALand the lowest content of Fe, Al, silt and clay among all the soils studied. The P affinity constant (k) was correlated positively and significantly to clay content (r = 0.66; P < 0.05), whereas mbc was correlated positively and significantly to clay content (r = 0.63; P < 0.05) and ammonium oxalate-extractable Fe (Fe_ox) (r = 0.63; P < 0.05). Phosphorus desorption of the soils varied widely depending on the initial P status and texture of the soils. Phosphorus desorbed by NH₄-lactate was many fold higher as compared to CaCl₂ in most soils.     

Natural rubber composites reinforced with sisal/oil palm hybrid fibers: Tensile and cure characteristics

Natural rubber was reinforced with untreated sisal and oil palm fibers chopped to different fiber lengths. The influence of fiber length on the mechanical properties of the hybrid composites was determined. Increasing the fiber length resulted in a decrease in the properties. The effects of concentration on the rubber composites reinforced with sisal/oil palm hybrid fibers were studied. Increasing the concentration of fibers resulted in a reduction in the tensile strength properties and tear strength but an increase in the modulus of the composites. Fiber breakage analysis was evaluated. The vulcanization parameters, processability characteristics, and stress–strain properties of these composites were analyzed. The extent of fiber alignment and the strength of the fiber–rubber interface adhesion were analyzed from the anisotropic swelling measurements. Scanning electron microscopy studies were performed to analyze the fiber/matrix interactions. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2305–2312, 2004