共查询到18条相似文献,搜索用时 78 毫秒
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流化床喷雾造粒颗粒强度的影响因素研究 总被引:1,自引:0,他引:1
颗粒强度作为流化床喷雾造粒产品的重要评价指标,对其影响因素的实验研究具有重要的现实意义。本文在一间歇锥形流化床喷雾造粒器中,以食用小麦淀粉为原料,以明胶的水溶液为粘结剂,实验研究了流化气速、床层温度、喷嘴雾化空气压力、粘结剂浓度对喷雾造粒颗粒强度的影响。结果表明,在本实验范围内,流化气速对颗粒强度的影响显著,床层温度、粘结剂浓度对颗粒强度也有较大的影响,而且均是非单调的。但喷嘴雾化空气压力与颗粒强度之间存在正向相关性。 相似文献
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在粉体制备的实际生产过程中,分级机是保证产品质量的重要环节,特别是在微粉窄级别物料的生产中尤为重要。这是因为窄级别物料要求产品的粒度分布很窄,即不能有大颗粒的存在,细颗粒含量也不能过多。这就要求分级机不但能去除物料中的大颗粒,而且要控制物料中的细颗粒... 相似文献
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大豆蛋白液喷雾场粒度分布变化 总被引:1,自引:0,他引:1
目的研究大豆蛋白液喷雾场粒度分布的变化规律,为选择一个合适的蔬菜纸喷涂面提供实验数据,以期得到质量好的蔬菜复合纸覆膜。方法将大豆蛋白喷涂雾化场网格化,使用粒度仪分别测量各个区域的粒径和粒度占比分布。结果雾化场轴向距离从H=10 cm处的95μm左右,到H=15 cm处的85μm左右,到H=20 cm处的65μm左右,再到H=30 cm处的45μm左右,最大粒径占比范围逐渐降低;雾化场径向距离从L=4 cm处的40~50μm,到L=8 cm处的35~40μm,到L=12 cm处的35~40μm,再到L=16 cm处的30~35μm,最大粒径占比范围也逐渐降低;在相同的喷涂气压、喷涂液压下,随着轴向距离的增加,大豆蛋白液液滴粒径分布范围的减小,大粒径大豆蛋白液液滴的比例逐渐减少,粒径分布朝着小粒径方向靠拢,大豆蛋白液液滴粒径分布曲线越来越陡峭;在喷涂气压、喷涂液压不变的情况下,仅仅改变大豆蛋白液的粘度,在相同的喷雾场位置随着大豆蛋白液粘度的减小,粒度分布朝小粒径方向靠拢,小粒径大豆蛋白液液滴比例逐渐减小。结论喷涂气压越大、大豆蛋白液粘度越小,雾化效果越好,而喷涂液压对雾化效果影响不大;大豆蛋白液喷雾场液滴的粒径分布随着喷雾贯穿距离的增加,小粒径液滴所占比例逐渐增加,粒径分布曲线朝小粒径方向发展,同时随着垂直与喷雾轴心线径向距离的增加,小粒径液滴所占百分比也增加,粒径分布曲线朝着小粒径方向发展。 相似文献
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粉体粒度分布的分形研究 总被引:10,自引:0,他引:10
本文应用分形几何理论,研究了粉体的粒度分布特征,发现在双对数坐标下,许多材料粒径的重量累积百分含量与粒径之间呈直线关系,表明其粒度分布具有分形结构。分维可作为描述粉体粒度分布特征的一个序参量,其大小反映了粉体颗粒的组细程度和集中、不均匀特征,即粉体粒度分布空间结构性。并在监控粉磨机械效率、估测颗粒级配等方面有重要意义。 相似文献
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粉体粒度分布的分形特征 总被引:19,自引:0,他引:19
应用分形几何理论,研究了粉体的粒度分布特征,发现在双对数坐标下,许多材料粒径的重量积百分含量与粒长之间呈直线关系。表明其粒度分布具有分形结构,分维可作为粒度分布特征的一个序参量,它反映了粉体颗粒的粗细程度和集中、均匀特性。 相似文献
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《Drug development and industrial pharmacy》2013,39(11):1167-1176
The purpose of the present study was to apply melt granulation in a fluidized bed dryer (fluidized bed dryer melt granulation) to manufacture one-step effervescent granules composed of anhydrous citric acid and sodium bicarbonate to make tablets. This study permitted us to establish that such process parameters as concentrations of polyethylene glycol (PEG) 6000, residence times in the fluidized bed dryer, fineness of PEG6000, fineness of initial mixture effervescent systems, and efficiency of two lubricants markedly affect some granule and tablet characteristics. It is a dry process that is simple, rapid, effective, economical, reproducible, and particularly adapted to produce effervescent granules that are easily compressed into effervescent tablets. 相似文献
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《Drug development and industrial pharmacy》2013,39(10):1295-1302
ABSTRACTSlow-release matrix granules were manufactured in the fluidized bed using an aqueous dispersion of quaternary poly(meth)acrylates (Eudragit® RS 30 D) as binder for granulation. A factorial design was carried out to investigate the influence of the following parameters, spraying rate, applied polymer amount, and inlet air temperature, on various granule properties. Prerequisites for a slow release of the model drug theophylline are high spraying rate, high amount of polymer, and low inlet air temperature. No considerable decrease of the drug release rate can be achieved without a subsequent curing of the dry granules. A clear correlation exists between the moisture content of the fluidized bed, indicated by the terminal moisture content (TMC), and the mean dissolution time for 80% of the drug (MDT80). 相似文献
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《Drug development and industrial pharmacy》2013,39(1):47-55
In this study many parameters were screened for a small-scale granulation process for their effect on the yield of granules between 75 and 500 μm and the geometrical granule mean size (d50). First a Plackett-Burman design was applied to screen the inlet air temperature, the inlet flow rate, the spray rate, the nozzle air pressure, the nozzle spray diameter, and the nozzle position. The Plackett-Burman design showed that the key process parameters were the inlet flow rate and the spray rate and probably also the inlet air temperature. Afterward a fractional factorial design (25?2) was applied to screen the remaining parameters plus the nozzle aircap position and the spraying time interval. The fractional factorial design showed that the nozzle air pressure was also important. As the target values for the granule yield (between 75 and 500 μm) and the geometric mean granule size (between 300 and 500 μm) were reached during the screening experiments, further optimization was not considered necessary. 相似文献
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《Drug development and industrial pharmacy》2013,39(10):1529-1543
AbstractThere are many parameters affecting the properties of the final granules prepared in a fluidized bed. In this study one of the product parameters, quantity of the binder, has been studied for its effect on the final granule size, size distribution and friabilityDetermination of granule size change as a function of binder quantity leaded us to study the growth mechanisms during fluidized bed granulation. Two mechanisms are suggested;1) Snowballing of primary granules (nuclei)2) Agglomeration of primary granulesIt has been shown that there is a critical amount of binder at which the formation of the primary granules comes to an end if more binder is added to the system. Then granule growth occurs by agglomeration of the primary granules. The physical properties of the granules formed before and after this critical binder concentration varies significantly 相似文献
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There are many parameters affecting the properties of the final granules prepared in a fluidized bed. In this study one of the product parameters, quantity of the binder, has been studied for its effect on the final granule size, size distribution and friability
Determination of granule size change as a function of binder quantity leaded us to study the growth mechanisms during fluidized bed granulation. Two mechanisms are suggested;
1) Snowballing of primary granules (nuclei)
2) Agglomeration of primary granules
It has been shown that there is a critical amount of binder at which the formation of the primary granules comes to an end if more binder is added to the system. Then granule growth occurs by agglomeration of the primary granules. The physical properties of the granules formed before and after this critical binder concentration varies significantly 相似文献
Determination of granule size change as a function of binder quantity leaded us to study the growth mechanisms during fluidized bed granulation. Two mechanisms are suggested;
1) Snowballing of primary granules (nuclei)
2) Agglomeration of primary granules
It has been shown that there is a critical amount of binder at which the formation of the primary granules comes to an end if more binder is added to the system. Then granule growth occurs by agglomeration of the primary granules. The physical properties of the granules formed before and after this critical binder concentration varies significantly 相似文献