Crack-Bridging Analysis for Alumina Ceramics under Monotonic and Cyclic Loading

Frictional degradation of grain-localized bridges behind a crack tip has been recognized as the major cyclic fatigue mechanism in alumina ceramics. Such a fatigue mechanism implies that the crack growth resistance ( R ) curve behavior during cyclic fatigue is different from that of monotonic loading due to the reduction in crack-tip shielding. A recent crack-bridging theory based on crack compliances is used to study the bridging stresses under monotonic loading and during cyclic fatigue. The bridging-stress distributions of two coarse-grained aluminas under monotonic loading are determined using compliance measurements. Because the interlocking grain bridges at the crack wake are subject to frictional damage from cyclic loading, the bridging-stress distribution evaluated during cyclic fatigue is distinct from that for monotonic loading. These results indicate that it is incorrect to incorporate the R -curve behavior from monotonic loading to the analysis of cyclic fatigue of alumina ceramics.     

Crystallization behavior of oxyethylene/oxybutylene diblock and triblock copolymers

The crystallization behavior of poly(oxyethylene)-b-poly(oxybutylene) block copolymers with different compositions, morphologies and architectures (E_mB_n diblock copolymers and E_mB_nE_m, B_nE_mB_n triblock copolymers) were investigated and the effect of volume fraction and architecture on the crystallization temperature (T_c) in non-isothermal crystallization was determined. It is found that the E_mB_n diblock copolymers having long E blocks exhibit similar crystallization temperatures, irrespective of volume fraction and morphology, but for the block copolymers with shorter E blocks the crystallization temperature increases with both the volume fraction, φ_E, and the length, m, of the E block. Some block copolymers with extremely low T_c, which fall into the temperature range normally associated with homogenous nucleation, were chosen for time-resolved small-angle X-ray scattering (SAXS) and isothermal crystallization kinetics experiments. The results show that breakout crystallization occurs in all these block copolymers. Therefore, unlike E_mB_n/B_h blends, there is no obvious relationship between T_c and crystallization behavior in neat block copolymers and homogeneous nucleation does not definitely lead to confined crystallization. The values of χ_c/χ_ODT for all the block copolymers with hex and bcc morphology were also calculated. It is found that all the block copolymers have χ_c/χ_ODT<3, in agreement with the previously reported critical value and consistent with their breakout crystallization behavior.     

Mechanical properties of Mg(OH)2/polypropylene composites modified by functionalized polypropylene

Modified Mg(OH)₂/polypropylene (PP) composites were prepared by the addition of functionalized polypropylene (FPP); and acrylic acid (AA) and by the formation of in situ FPP. The effects of the addition of FPP and AA and the formation of in situ FPP on the mechanical properties of Mg(OH)₂/PP composites were investigated. Experimental results indicated that the addition of Mg(OH)₂ markedly reduced the mechanical properties of PP. The extent of reduction in notch impact strength of PP was higher than that in flexural strength and tensile strength. However, tensile modulus and flexural modulus increased with increased Mg(OH)₂ content. The addition of FPP facilitated the improvement in the flexural strength and tensile strength of Mg(OH)₂/PP composites. The higher the Mg(OH)₂ content was, the more significant the effect of FPP was. The incorporation of AA resulted in further increased mechanical properties, in particular the flexural strength, tensile strength, and notch impact strength of Mg(OH)₂/PP composites containing high levels of Mg(OH)₂. It not only improved mechanical properties but also increased the flame retardance of Mg(OH)₂/PP composites. Although the mechanical properties of composites modified by the formation of in situ FPP were lower than those of composites modified by only the addition of AA in the absence of diamylperoxide, the mechanical properties did not decline with increased Mg(OH)₂ content. Moreover, the mechanical properties increased with increasing AA content. The addition of an oxidation resistant did not influence the mechanical properties of the modified Mg(OH)₂/PP composites. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2139–2147, 2003     

Fracture morphology of Mg(OH)2/polypropylene composites modified by functionalized polypropylene

The morphologies of the fracture surface under impact and flexural testing of Mg(OH)₂/Polypropylene (PP) composites and their modified composites were investigated by scanning electron microscopy. Experimental results indicated that addition of functionalized polypropylene (FPP) and acrylic acid (AA) and the formation of in situ FPP changed the fracture morphologies of Mg(OH)₂/PP composites. We believe that addition of these modifiers improved the interfacial interaction and enhanced the interface adhesion between the particle and the matrix in Mg(OH)₂/PP composites. The degree of improvement was more significant in Mg(OH)₂/PP composites modified by the formation of in situ FPP. At low Mg(OH)₂ content, 2 phr AA exhibited a marked effect, but at high Mg(OH)₂ content, 4 phr AA afforded good effect. Due to the improved interface adhesion by interface interactions the fracture mechanism transformed from interface debonded fracture into a matrix fracture. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2148–2159, 2003     

Formulation for chemical EOR: Development and evaluation of an ASP formulation In customer field conditions

Alkali surfactant polymer (ASP) flooding is an enhanced oil recovery (EOR) technology with an impressive potential for increasing incremental oil production from conventional hydrocarbon bearing reservoirs. A challenge to ASP application is the complexity of determining an effective formulation, typically requiring extensive laboratory screening of nearly countless combinations of surfactants and cosolvents. This paper focuses on demonstrating the utility of the hydrophilic–lipophilic deviation (HLD) concept for EOR application to simplify surfactant formulation workstreams seeking an economically viable ASP formulation for field application. In describing work performed for EOR application of ASP under customer conditions using crude oil, the discussion covers the initial evaluation of the promising surfactant formulation (interfacial tension and solubility), the improvement upon the formulation via HLD principles, and the evaluation of the improved surfactant formulation (coreflood studies). The final ASP formulation identified consisted of a 9 to 1 mixture of alkyl propoxy sulfate sodium salt (APS) to alkyl ethoxy sulfate sodium salt (AES) totaling 2000 ppm active surfactant content, 2.0 wt% Na₂CO₃, and 3000 ppm polyacrylamide polymer (all commercially available products). This formulation had ultra-low interfacial tension and favorable mixing behavior under reservoir conditions. In coreflood studies, the final formulation reproducibly achieved cumulative oil recovery of 96.4%–98.5% of original oil in place with only 0.3 PV of ASP injection with a chase alkali polymer injection.     

Recent developments in the fire retardancy of polymeric materials

The widespread applications of polymeric materials require the use of conventional flame retardants based on halogen and phosphorous compounds to satisfy fire safety regulatory standards. However, these compounds, particularly halogen-based examples, are persistent organic pollutants of global concern and generate corrosive/toxic combustion products. To account for eco-friendliness, ultimate mechanical/physical properties and processing difficulties, the window of options has become too narrow. Although the incorporation of non-toxic nanofillers in polymers shows positive potential towards flame retardancy, many obstacles remain. Moreover, most of the literature on these materials is qualitative, and often points to conflicting/misleading suggestions from the perspectives of short-term and long-term fire exposure tests. Hence, there is a renewed need to fundamentally understand the fire response of such materials, and complement experimental results with theoretical modelling and/or numerical simulation.     

超声提取在蔬菜农药检测中的应用

目的：探讨超声提取法在蔬菜中有机磷、有机氯和菊酯类农药提取的应用.方法：采用超声提取法对添加有敌敌畏、二嗪磷、乐果、马拉硫磷、倍硫磷、水胺硫磷、乙硫磷、α-666、δ-666、PP’-DDE、pp’-DDT、联苯菊酯、氟氯氰菊酯的青瓜样品进行提取,添加最终浓度分别为0.05、0.1、0.15 μg/g,净化后用气相色谱仪（GC-FPD、GC-ECD）测定回收效果.结果：三个浓度的所有检测农药回收率在80％～110％之间,RSD少于10％,回收率和重复性良好.     

SIMULATION AND OPTIMIZATION OF COIL DECOKING IN ETHANE PYROLYSIS FURNACE

A detailed model of coupled heat transfer in the firebox and coke oxidation in the coils of a commercial ethane pyrolysis furnace was developed to simulate the decoking process. The model was created by combining a plug flow reactor model, the shrinking core model, and the zonal approach method to approximately describe the fluid flow in the coils, the gas-solid heterogeneous reactions of coke gasification, and the heat transfer in the furnace. The simulation accurately modeled the decoking time and CO₂ mole fraction at the coil outlets. The model may be used to evaluate existing decoking processes, and new decoking procedures can be investigated by iterative approximation. The model can be used to validate the following steady-state operating conditions: coil outlet temperature, coil inlet temperature, decoking time, coil outlet CO₂ mole fraction, and the maximum external tube wall temperature, resulting in lower consumption of steam and air and a reduction in residual coke. This work has provided essential information for the development of advanced on-line coke-burning procedures for ethylene production.     

制药工程专业《制药工程学》实验教学质量标准研究

文章介绍了《制药工程学》实验课程在培养学生工程实践能力中的的作用、特点,并根据目前实验教学的现状,提出了《制药工程学》课程实验教学的量化质量标准。初步试验表明,实施该质量标准取得了一定的成效。