Equilibrium of one-pot polymerization of polyimide

One-pot polymerization of polyimide from 3,3′,4,4′-biphenyl tetracarboxylic dianhydride (BPDA) and 4,4′-oxydianiline (ODA) was examined. The equilibrium in the polyimide with water was examined in detail in p-chlorophenol solution during the polymerization. The equilibrium constant was expressed by log K = 1.50 + 1433 (1/T). The polymerization reaction is exothermic. The molecular weight increased with decrease of temperature. © 1996 John Wiley & Sons, Inc.     

Properties of copolyimides prepared from different tetracarboxylic dianhydrides and diamines

Various copolymides were prepared from two acid dianhydrides (BPDA, 3,3′,4,4′-biphenyl tetracarboxylic dianhydride; PMDA, pyromelitic dianhydride) and two diamines (PPD, p-phenylene diamine; ODA, 4,4′-oxydianiline). The thermal and mechanical properties of these polyimides were examined in detail. By appropriately selecting the ratios of the acid dianhydride component and the diamine component, polyimide films having desirable mechanical and thermal characteristics can be obtained. Further, it was proved that there is a correlation between the properties and the compositions of the copolyimides and that the properties could be estimated from the compositions by the use of multiple regression analysis. © 1996 John Wiley & Sons, Inc.     

Reactive processing of thermoset/thermoplastic blends: A potential for injection molding

Poly(2,6-dimethyl-1,4-phenylene ether) (PPE) is an engineering plastic with high heat distortion temperature. Melt processing of neat PPE is usually accompanied with thermal degradation. The degradation problem is solved by blending with polystyrene to reduce the processing temperature. We propose an alternative using triallylisocyanurate (TAIC). TAIC is a low viscosity liquid that can be cured by peroxide, e.g. α,α′-bis(t-butylperoxy-m-isopropyl)benzene (PBP), to provide a thermoset. The PPE/TAIC mixture was shown to have the upper critical solution temperature (UCST) type phase behavior. At the single-phase regime above UCST and below the cure temperature (∼180°C for PBP), the mixture had a low viscosity, less viscous than a conventional thermoplastic such as PC and PP. That is, a nice window for injection molding was available, e.g., at 100°C to 160°C for a 50/50 blend. After injecting into a hot mold set at cure temperature, the blend cured in a short time (∼80% conversion in 5 min). Then the molded and partly cured material kept its shape and dimensions during post-cure in a hot chamber at higher temperature (e.g. 250°C). Using transmission electron microscopy and dynamic mechanical analyses, it was shown that the cured blend had a bicontinuous two-phase structure with periodic spacings of ∼30 nm, suggesting a structure formation via a spinodal decomposition driven by the increase in molecular weight of TAIC during cure. The cured material showed excellent flexural strength and high chemical resistance.     

Change in the Rheology of Starch Adhesive During Gelatinization

In this paper the viscosity increase of the starch paste during gelatinization is examined. Upon heating, raw starch granules gelatinize and the paste viscosity of the starch adhesive increases dramatically. Bonding develops further through the dehydration of the gelatinized starch by the board. Bond setting of carrier-type (mixture of dissolved and raw) starch on paperboard in the corrugated board operation is thought to result from a combination of thermal gelatinization and dehydration by the board.     

Inactivation of Bacillus spores by the combination of moderate heat and low hydrostatic pressure in ketchup and potage

The combination effect of moderate heat and low hydrostatic pressure (MHP) on the reduction of Bacillus subtilis, Bacillus coagulans and Geobacillus stearothermophilus spores in food materials (potage and ketchup) was investigated. These bacterial spores were suspended in potage (pH 7), acidified potage (pH 4), neutralized ketchup (pH 7) and ketchup (pH 4). The suspensions were treated with and without pressure (100 MPa) and temperatures of 65-85 degrees C for 3 to 12 h. The bacterial spores were inactivated by 4-8 log cycles during MHP treatment in potage, acidified potage and ketchup, whereas the spores were highly resistant to long time heat treatment in potage and neutralized ketchup. The degrees of spore destruction were mostly dependent on pH and medium composition during MHP treatment. The inactivation effect in MHP treatment was higher at the pH 7 than at pH 4 both in ketchup and potage. The bacterial spores showed higher inactivation in potage than ketchup during MHP treatment.     

Surface and pore structure of alumina derived from xerogel/aerogel

The alkyl derivatives of boehmite were prepared by solvothermal reaction of aluminum isopropoxide in n-alcohols (ethanol, 1-butanol, 1-hexanol, 1-octanol and 1-dodecanol) and the products were recovered as aerogel/xerogel by the removal of the solvent at the end of reaction. Aerogel or xerogel can be obtained simply by using only a reaction vessel (autoclave) and the obtained products were composed of plate-like particles having a well-developed boehmite structure. The alumina powders obtained by calcination of these products had relatively large pore-volumes ranging from 1.35 to 2.56 cm³/g. Transformation into α-Al₂O₃ was retarded even after calcination at 1200 °C. The effect of n-alcohols used in the solvothermal reaction on the phase, morphology and pore-texture of the alumina samples are discussed.     

Steam Reforming of Methanol on Copper Catalysts Supported on Large-Surface-Area ZnAl2O3

Steam reforming of methanol on various supported Cu catalysts was examined. Supports strongly affected catalyst activity and, among the catalysts tested, Cu catalyst supported on large-surface-area ZnAl₂O₄ showed the highest activity, which, to the best of our knowledge, was higher than those for the supported catalysts reported so far. For supported Cu catalysts, two species were observed. One was a dispersed Cu species having strong interaction between Cu and support, and the other was an isolated Cu species. The activity of the former species strongly depended on supports.     

PMMA-SiO2杂化材料对天然橡胶的增强作用

提取了活性硅烷醇,用自由基共聚合法成了含硅高聚物,分析了SiO2含量对硫化天然橡胶力学性能的影响。     

Synthesis of CeO2-ZrO2 solid solution by glycothermal method and its oxygen release capacity

The glycothermal (GT) reaction of Ce acetate and Zr alkoxide directly yielded CeO₂-ZrO₂ solid solutions in a region of low Ce content ≤40 mol%. Of the CeO₂-ZrO₂ solid solutions obtained by the GT method and subsequent calcination at 500 or 800 °C, the sample with 20 mol% Ce content had the largest BET surface area. This sample exhibited the highest Ce-based oxygen release capacity in the whole Ce/Zr composition range. The oxygen release capacities of CeO₂-ZrO₂ solid solutions synthesized by the GT method were much larger than those of the samples prepared by a coprecipitation (CP) method. The Reitveld analysis and the repetitive reduction-oxidation experiment indicated that the CeO₂-ZrO₂ solid solution synthesized by the GT method has a homogeneous structure as compared with that prepared by the CP method.     

Effect of steric hindrance on hydrogen‐bonding interaction between polyesters and natural polyphenol catechin

The phase behaviors for the blends of poly(3‐hydroxypropionate) (PHP), poly(L ‐lactide) (PLLA), poly(D ‐lactide) (PDLA), and poly(D,L ‐lactide) (PDLLA) with catechin were investigated by differential scanning calorimetry. In PLLA/catechin, PDLA/catechin, and PDLLA/catechin blends, two glass transitions were detected when the catechin content was ≥40 wt %, whereas in PHP/catechin blends only one glass transition was observed over the whole range of blend compositions. The former and the latter results should reflect the inhomogeneous and the homogeneous nature of the blends, respectively, in the amorphous phase. These different phase behaviors should arise from the differences in the chemical structures between PHP and PLLA/PDLA/PDLLA, which dominates the strength and the number of intermolecular hydrogen‐bonding interactions between the ester carbonyl groups of polyesters and the phenol groups of catechin. As detected by FTIR spectroscopy, in comparison with PHP, the steric hindrance of side‐chain methyl groups of PLLA, PDLA, and PDLLA might restrain the formation of hydrogen bonds between their ester carbonyl groups and the phenol hydroxyl groups of catechin, even weakening the strength of such hydrogen bonds. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3565–3573, 2004