Coronary artery fistula after cardiac transplantation

A cardiac transplant recipient with multiple coronary artery fistulae draining into the right ventricle is described. These fistulae presumably resulted from repeated endomyocardial biopsies. The diagnosis of coronary artery fistulae was made at the annual coronary arteriography. The magnitude of the shunt remained small over eight years of follow-up.     

Starch–poly(ethylene-co-acrylic acid) composite films. Effect of processing conditions on morphology and properties

Formulations containing 4 parts cornstrach, 5 parts poly(ethylene-co-acrylic) (EAA), 1 part urea, and 1.6 parts of either water or aqueous ammonia were extruded at either 110–120°C or 150–160°C; and the resulting extrudates were then extrusion-blown into films. Complex formation between EAA and starch was measured by either X-ray diffraction or by solvent extraction of uncomplexed EAA. Although the processing temperature had only a minor effect on the amount of EAA complexed by starch, use of aqueous ammonia rather than water in these formulations increased the amount of complexed EAA by about a factor of 2. In films prepared with aqueous ammonia, the polysaccharide phase was present as submicron-sized domains. When ammonia was omitted from these formulations, the polysaccharide phase was less uniform in size and contained particles that were over an order of magnitude larger than those observed with ammonia.     

Nanograin magnetoresistive manganite coatings for EMI shielding against directed energy pulses

Two magnetoresistive manganites, La_0.83Sr_0.17MnO₃ and La_0.7Sr_0.3MnO₃, are synthesized by the environmentally friendly “deposition by aqueous acetate solution (DAAS)” technique. The manganite film has a grain size of 100 nm, and can be processed as thinly as 0.03 μm per layer, while the powder form has a crystallite size of 40 nm. These magnetoresistive materials are shown to be effective and inexpensive electromagnetic interference (EMI) shield for the extremely low frequency (ELF) EM fields. The electrical resistance of manganites is very sensitive to external influences, such as temperature and electromagnetic fields. Both permeability (μ) and conductivity (σ) of manganites tend to increase with increasing applied magnetic field. The manganites have been shown to “react” to field increases in a way that is particularly useful for shielding EMI field fluctuations (e.g., due to current or voltage spikes).

The manganite properties, e.g., crystal structure, film morphology, radiation absorption and reflection, electrical resistivity, and magnetization, etc., have been measured. The ceramic manganites have a metal–insulator transition at 300 K or higher, and are suitable for a room temperature operation. A thin film (approx. 0.1 μm) of La_0.83Sr_0.17MnO₃ was fabricated on a quartz tube or refractory ceramic fiber blanket. Using this thin manganite film, the EMI shielding effectiveness for the measured E-field attenuation is similar to that of a 25 μm thickness of copper tube, aluminum foil, and silver–nickel particle-dispersed paper. The silver–nickel impregnated paper has an EMI shielding effectiveness of 35 dB at 10 kHz, and 15 dB at 60 Hz (or frequency above 1 MHz). The ceramic manganites are chemically inert, thermally stable, and mechanically flexible. They provide low cost EMI shielding against directed energy pulses and may serve as a “signature reduction” barrier.     

Updated Correlation Between Aircraft Smoke Number and Black Carbon Concentration

Aircraft emissions of black carbon (BC) contribute to anthropogenic climate forcing and degrade air quality. The smoke number (SN) is the current regulatory measure of aircraft particulate matter emissions and quantifies exhaust plume visibility. Several correlations between SN and the exhaust mass concentration of BC (C _BC) have been developed, based on measurements relevant to older aircraft engines. These form the basis of the current standard method used to estimate aircraft BC emissions (First Order Approximation version 3 [FOA3]) for the purposes of environmental impact analyses. In this study, BC with a geometric mean diameter (GMD) of 20, 30, and 60 nm and filter diameters of 19 and 35 mm are used to investigate the effect of particle size and sampling variability on SN measurements. For BC with 20 and 30 nm GMD, corresponding to BC emitted by modern aircraft engines, a smaller SN results from a given C _BC than is the case for BC with 60 nm GMD, which is more typical of older engines. An updated correlation between C _BC and SN that accounts for typical size of BC emitted by modern aircraft is proposed. An uncertainty of ±25% accounts for variation in GMD in the range 20–30 nm and for the range of filter diameters. The SN–C _BC correlation currently used in FOA3 underestimates by a factor of 2.5–3 for SN ≤15, implying that current estimates of aircraft BC emissions derived from SN are underestimated by the same factor.

Copyright 2013 American Association for Aerosol Research     

Layered double hydroxide platelets exfoliation into a water‐based polyester

Nitrate layered double hydroxide (LDH) phase Zn₂Al(OH)₆(NO₃)·2H₂O is successfully exfoliated in the presence of polyester under mild conditions using water as essential solvent and at room temperature under air. From small angle X‐ray scattering spectroscopy a total exfoliation is found to be achieved using up to 10 wt % LDH, while intercalated polymer nanocomposite structures largely extended up to 14 nm are observed for loading ranging from 10 to 20 wt %. The process is found to be explained by the diffusion of the polymer chain into the interlayer host structure. Starting from an initial value of 0.89 nm, ≈3, 7, 10, 14, and 20 nm transient interleaved nanostructures are formed without any carbonate uptake. The collective gap distance is certainly due to a defined number of polymer chains diffusing into the LDH interstices. Similarly, starting from an aqueous polyester solution highly concentrated in LDH nitrate phase up to 50% w.w, successive dilutions yield platelet exfoliation, thus rendering a smooth chemistry process attractive for potential applications. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

水热沉积电压对C-AlPO_4涂层显微结构的影响

以方石英型磷酸铝(C-A1PO4)粉体为原料,异丙醇为溶剂,碘为荷电介质,采用水热电泳沉积方法在涂有SiC涂层的碳纤维增强碳(C/C-SiC复合材料表面制备了C-A1PO4外涂层.借助X射线衍射和扫描电镜表征了涂层的晶相组成和显微结构.研究了沉积电压对C-A1PO4涂层显微结构的影响,并测试了涂层的抗氧化性能.结果表明:在180～220V范围内,水热沉积电压对涂层的显微结构有较大的影响,220V时制备的涂层致密均匀.涂层的沉积量以及涂层与基体的结合强度随着沉积电压的升高而增加;单位面积沉积量与时间的二次方根之间符合线性关系.与包埋法制备的SiC涂层相比,水热电泳沉积法制备的C-A1PO4涂层具有更好的抗氧化性能,涂层样品在1500℃的空气中氧化37h后质量损失仅为0.53%.     

注射成型中浇口形式对塑件质量的影响

用生产实例介绍了不同浇口形式及位置对塑料熔体在型腔中的填充模式和注射成型后塑件的内在机械物理性能及表观质量的影响。     

High hydrostatic pressure modification of whey protein concentrate for improved functional properties

Whey protein concentrate (WPC) has many applications in the food industry. Previous research demonstrated that treatment of whey proteins with high hydrostatic pressure (HHP) can enhance solubility and foaming properties of whey proteins. The objective of this study was to use HHP to improve functional properties of fresh WPC, compared with functional properties of reconstituted commercial whey protein concentrate 35 (WPC 35) powder. Fluid whey was ultrafiltered to concentrate proteins and reconstituted to equivalent total solids (8.23%) as reconstituted commercial WPC 35 powder. Solutions of WPC were treated with 300 and 400 MPa (0- and 15-min holding time) and 600 MPa (0-min holding time) pressure. After HHP, the solubility of the WPC was determined at both pH 4.6 and 7.0 using UDY and BioRad protein assay methods. Overrun and foam stability were determined after protein dispersions were whipped for 15 min. The protein solubility was greater at pH 7.0 than at pH 4.6, but there were no significant differences at different HHP treatment conditions. The maintenance of protein solubility after HHP indicates that HHP-treated WPC might be appropriate for applications to food systems. Untreated WPC exhibited the smallest overrun percentage, whereas the largest percentage for overrun and foam stability was obtained for WPC treated at 300 MPa for 15 min. Additionally, HHP-WPC treated at 300 MPa for 15 min acquired larger overrun than commercial WPC 35. The HHP treatment of 300 MPa for 0 min did not improve foam stability of WPC. However, WPC treated at 300 or 400 MPa for 15 min and 600 MPa for 0 min exhibited significantly greater foam stability than commercial WPC 35. The HHP treatment was beneficial to enhance overrun and foam stability of WPC, showing promise for ice cream and whipping cream applications.