Digital X-ray Imaging Technique to Study the Horizontal Injection of Gas-Liquid Jets into Fluidized Beds

Gas-liquid jets injected into fluidized beds of particles/catalyst find applications in many industrial processes. The effective distribution and mixing of the feed droplets with the entrained bed particles is vital in improving the process efficiency. The present study utilizes a sophisticated digital X-ray imaging system to study the internal flow structure of jets injected into fluidized beds. The system is equipped with an X-ray image intensifier (XRII) and optical detectors, which convert the transmitted X-ray photons into digital images of up to 60 frames s-1. The imaging technique provides useful information such as the jet expansion angle and the penetration distance. These are functional quantities in optimizing the performance of feed nozzles, and in modeling the jet-fluidized bed interactions. In this work, the horizontal injection of gas, gas-liquid, and liquid jets into fluidized beds is investigated. The results indicate that the jet expansion (half-angle) is considerably reduced for a gas-liquid jet (5-7 degrees) when compared to that of a gas jet (10-15 degrees). The gas-liquid jet also appears to penetrate more than a gas jet with the same momentum. When a liquid feed is introduced into a fluidized bed of particles, the particles may agglomerate if they are wet-enough to form liquid bridges. Improper feed distribution may be a direct contributor to enhanced agglomeration. In this regard, radio-opaque tracers mixed with the feed liquid are injected to track the formation and the movement of agglomerates. The tracer experiments show that the agglomerates are generated at the end of the jet region, close to its maximum penetration distance. A brief discussion on the modifications required to achieve improved contrast for the acquired images, and the effect of some important X-ray parameters are also included in the present study

Ectopic spinal calcification associated with diffuse idiopathic skeletal hyperostosis (DISH): A quantitative micro-ct analysis

Diffuse idiopathic skeletal hyperostosis (DISH) is a non-inflammatory spondyloarthropathy identified radiographically by calcification of the ligaments and/or entheses along the anterolateral aspect of the vertebral column. The etiology and pathogenesis of calcifications are unknown, and the diagnosis of DISH is currently based on radiographic criteria associated with advanced disease. To characterize the features of calcifications associated with DISH, we used micro-computed tomographic imaging to evaluate a cohort of 19 human cadaveric vertebral columns. Fifty-three percent of the cohort (n=10; 3 females, 7 males, mean age of death=81 years, range 67-94) met the radiographic criteria for DISH, with calcification of four or more contiguous vertebral segments. In almost all cases, the lower thoracic regions (T8-12) were affected by calcifications, consisting primarily of large, horizontal outgrowths of bony material. In contrast, calcifications localized to the upper thoracic regions demonstrated variability in their presentation and were categorized as either continuous vertical bands or discontinuous-patchy lesions. In addition to the variable morphology of the calcifications, our analysis demonstrated remarkable heterogeneity in the densities of calcifications, ranging from internal components below the density of cortical bone to regions of hyper-dense material that exceeded cortical bone. These findings establish that the current radiographic criteria for DISH capture heterogeneous presentations of ectopic spine calcification that can be differentiated based on morphology and density. These findings may indicate a naturally heterogenous disease, potential stage(s) in the natural progression of DISH, or distinct pathologies of ectopic calcifications. (c) 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Re

Effect of Memantine Treatment and Combination with Vitamin D Supplementation on Body Composition in the APP/PS1 Mouse Model of Alzheimer\u27s Disease following Chronic Vitamin D Deficiency

Background: Vitamin D deficiency and altered body composition are common in Alzheimer\u27s disease (AD). Memantine with vitamin D supplementation can protect cortical axons against amyloid-ß exposure and glutamate toxicity. Objective: To study the effects of vitamin D deprivation and subsequent treatment with memantine and vitamin D enrichment on whole-body composition using a mouse model of AD. Methods: Male APPswe/PS1dE9 mice were divided into four groups at 2.5 months of age: the control group (n=14) was fed a standard diet throughout; the remaining mice were started on a vitamin D-deficient diet at month 6. The vitamin D-deficient group (n=14) remained on the vitamin D-deficient diet for the rest of the study. Of the remaining two groups, one had memantine (n=14), while the other had both memantine and 10 IU/g vitamin D (n=14), added to their diet at month 9. Serum 25(OH)D levels measured at months 6, 9, 12, and 15 confirmed vitamin D levels were lower in mice on vitamin D-deficient diets and higher in the vitamin D-supplemented mice. Micro-computed tomography was performed at month 15 to determine whole-body composition. Results: In mice deprived of vitamin D, memantine increased bone mineral content (8.7% increase, p\u3c0.01) and absolute skeletal tissue mass (9.3% increase, p\u3c0.05) and volume (9.2% increase, p\u3c0.05) relative to controls. This was not observed when memantine treatment was combined with vitamin D enrichment. Conclusion: Combination treatment of vitamin D and memantine had no negative effects on body composition. Future studies should clarify whether vitamin D status impacts the effects of memantine treatment on bone physiology in people with AD