Preparation,morphology, and properties of multilamellar barrier materials based on blends of high‐density polyethylene and copolyester

The multilamellar barrier materials based on the blends of high‐density polyethylene (HDPE) and copolyester (PETG) were prepared via melt extrusion, and poly(ethylene‐co‐acrylic acid) (EAA) as a compatibilizer was incorporated into the blends. A systematic investigation was carried out, with regard to morphology and properties. Scanning electron microscopy observation displayed the laminar morphology for the blends with the whole compositions, and the thinner laminas of the PETG phase formed in the HDPE matrix by incorporating EAA into the blends. In addition, the number and the size of the laminas of the dispersed phases were also dependant on the die temperature and screw speed, respectively. Evaluation of the mechanical properties demonstrated that incorporation of the EAA resulted in an improvement of the mechanical properties. These behaviors are attributed mainly to better adhesion and compatibility between HDPE and PETG, which has been confirmed by thermal analysis and the rheological properties. On the basis of these premises, it is reasonable to suggest that the improved barrier properties of the ternary blends with increasing concentration of the EAA be attributed to both the increase in the number of the laminas of the PETG and the decrease in their thickness, which prohibits the organic solvent molecules from entering into and permeating through the amorphous regions of the blends. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3791–3799, 2006     

Study of a downward gas jet in a two–dimensional fluidized bed

The study of a downward gas jet was performed in a two–dimensional (2–D) fluidized bed of sand particles under conditions of minimum fluidization and at atmospheric pressure and room temperature. The jet shifted through a cyclic sequence of left–central–right–central–left positions. The probability of the left and right jets was 40% each, while the less stable central jet occurred only 20% of the time. Discrete probability distributions of jet presence for each of the three jet configurations and an overall distribution are presented. They show that jets are dominant along the external walls of the nozzle. The depth of the downward jet increased with air flowrate in agreement with the correlation from Massimilla and Russo (1973).     

Ultrapyrolysis of automobile shredder residue

A fast pyrolysis (Ultrapyrolysis) process was employed to convert automobile shredder residue (ASR) into chemical products. Experiments were conducted at atmospheric pressure and temperatures between 700 and 850°C with residence times between 0.3 and 1.4 seconds. Pyrolysis products included 59 to 68 mass% solid residue, 13 to 23 mass% pyrolysis gas (dry) and 4 to 12 mass% pyrolytic water from a feed containing 39 mass% organic matter and 2 mass% moisture. No measurable amounts of liquid pyrolysis oil were produced. The five most abundant pyrolysis gases, in vol%, were CO (18–29), CO₂ (20–23), CH₄ (17–22), C₂H₄ (20–22) and C₃H₆ (1–11), accounting for more than 90% of the total volume. The use of a higher organic content ASR feed (58 mass%) resulted in less solid residue and more pyrolysis gas. However, no significant changes were noted in the composition of the pyrolysis gas.     

Foaming and chain extension of completely biodegradable poly(propylene carbonate) using DPT as blowing agent

Completely biodegradable foams of poly(propylene carbonate) (PPC) derived from carbon dioxide and propylene oxide were fabricated using N, N′-dinitroso pentamethylene tetramine (DPT) as chemical blowing agent, and urea as the activator to lower the decomposition temperature of DPT. Thermal decomposition behavior and gas evolution behavior of the DPT composite with various urea to DPT ratios were investigated to optimize the composition of the blowing agent. The formulation of blowing agent mixture and foaming condition, the foam morphologies, the molecular weight change, as well as the mechanical properties of produced PPC foams were studied extensively. The experimental results demonstrated that the greatest blowing ratio of 14.8 can be afforded in case 12 phr blowing agent was used at 170 °C for 30 min. Gel permeation chromatography (GPC) and thermal analysis revealed that DPT acted as both chain-extension agent and blowing agent for PPC matrix. The molecular weight of PPC subjected to foaming increased by 76%. The foamed PPC exhibited superior mechanical properties and can be used as packaging material for many practical applications.     

Pozzolanic properties of reject fly ash in blended cement pastes

Low-grade fly ash (reject fly ash, r-FA), a significant portion of the pulverized fuel ash (PFA) produced from coal-fired power plants and rejected from the ash classifying process, has remained unused due to its high carbon content and large particle size. But it may be used in certain areas, such as in solidification and stabilization processes of hazardous waste and materials for road base or subbase construction, which require relatively lower strength and reactivity. It is therefore necessary to extend research on the properties of r-FA and explore its possible applications. This paper presents experimental results of a study on the mechanical and hydration properties of cementitious materials prepared by blending r-FA with ordinary Portland cement (OPC). Parallel mixes were also prepared with the good ash [i.e., classified fine fly ash (f-FA)] for comparison. Selective chemical activators were added to the mix to study the effects of the activators on the properties of the blend system. The results show that r-FA generally has a lower rate of hydration than f-FA particularly at the early stage of hydration. Adding Ca(OH)₂ alone almost had no effect on accelerating the hydration of r-FA. But adding a small quantity of Na₂SO₄ or K₂SO₄ together with Ca(OH)₂ significantly accelerated the hydration reaction. The results of the compressive strength measurement correlated nicely with the degree of hydration results. It was also found that water-to-binder ratio (w/b) was an important factor in affecting the strength development and the hydration degree of r-FA pastes.     

卤水法制硫酸钡产品中的氯、硼含量测定

卤水法制硫酸钡在生产过程中吸附、包裹了许多无机离子，严重影响了产品的质量与应用。为了及时了解产品性能，提高产品质量，通过大量实验，建立此方法。论述了一种测定硫酸钡中氯、硼两种杂质离子含量的方法。此法准确、精密度高，实测样品中氯和硼的回收率分别为98．2％和102．1％，相对标准偏差（n=5）分别为1.53％和2.22％。测定结果与原子吸收分光光度法测定结果一致，且快速、简便，可作为卤水法制硫酸钡产品中的氯、硼含量测定方法。     

纺速对聚酯工业丝干热收缩率的影响

通过对不同纺速的高粘聚酯初生丝的结构的测试,探讨了初生纤维结构随纺速变化的规律,以及初生丝的结构对成品工业丝的干热收缩率的影响。     

Possible effects of site isolation in antimony oxide-modified vanadia/titania catalysts for selective oxidation of o-xylene

Titania-supported vanadia catalysts were modified by addition of antimony oxide for application in o-xylene selective oxidation to phthalic anhydride. It was shown that active and selective catalysts can be prepared by ball-milling mixtures of powders of TiO₂, V₂O₅and Sb₂O₃followed by calcination. X-ray photoelectron spectroscopy proves the formation of highly dispersed overlayers of vanadium oxide and antimony oxide, in which V⁵⁺is partially reduced to lower oxidation states and Sb³⁺is partially oxidized to Sb⁵⁺. Antimony oxide segregated into the outermost surface layers. It is therefore inferred that the presence of the antimony oxide modifier spatially separates V–O species and leads to site isolation which may be responsible for the positive effect of the modifier for the catalyst's selectivity.     

Investigation of free volume,interfacial, and toughening behavior for cyanate ester/bentonite nanocomposites by positron annihilation

Effects of filler on microstructure and toughening behavior of cyanate ester (CE)/bentonite (BT) nanocomposites with different content of BT have been studied by positron annihilation lifetime spectroscopy, X‐ray diffraction, transmission electron microscopy, dynamic mechanical analysis, etc. The interesting results found by PALS indicate that the size and concentration of the free volume holes and the apparent free volume fraction increased with increasing the content of BT, which indicates that adding nano‐layers to thermosetting materials can lead to the high crosslinking density structure “looser.” The experimental results reveal that the increases in size of free volume holes and apparent free volume fraction are related to the increasing conversion of cure reaction. On the other hand, the mechanism of toughening (by adding the nano‐clay to the thermosetting material) has been discussed by combining free volume and interfacial property. It is shown that, for the high crosslinking thermosetting material‐based nanocomposites, both the property of free volume and dispersion state of nano‐layers are the two key factors in determining toughening property. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1509–1515, 2006