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采用超临界CO2萃取花生油脂中主要成分,研究了萃取压力、萃取温度、萃取时间和夹带剂用量等对萃取率的影响。结果表明,在CO2流量为10~12 L/h的前提下,最佳工艺条件是:萃取温度45℃,萃取压力30 MPa,萃取时间2.0 h,夹带剂用量20 mL。在此条件下,花生油脂的萃取率可达50.39%。影响提取率的主次因素为萃取压力萃取时间萃取温度夹带剂用量。 相似文献
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超临界CO_2萃取烟草精油的工艺研究 总被引:1,自引:0,他引:1
以烟草为材料,以精油提取率、新植二烯提取率、精油品质为评价指标,通过单因素实验考察夹带剂乙醇的体积分数、夹带剂流量、萃取压力、萃取温度、CO2流量、萃取时间等因素对萃取效果的影响。在此基础上,通过正交实验优选萃取工艺条件为:94%乙醇为夹带剂、夹带剂流量0.04mL·min-1、萃取压力25MPa、萃取温度50℃、CO2流量2.0L·min-1、萃取时间3.0h,在此条件下萃取的精油金黄透亮,夹带剂残留少,精油提取率为37.58mg·g-1,新植二烯提取率为4.045mg·g-1。 相似文献
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用正交实验法优化采用超临界CO2技术萃取车前草中熊果酸的工艺条件。在单因素实验基础上,采取L9(3^3)探讨萃取压力、萃取温度、CO2流量对萃取车前草熊果酸的得率的影响情况,确定了超临界CO2萃取车前草中熊果酸的适宜条件。超临界萃取最优条件为:萃取压力35MPa,萃取温度为40℃,选择无水乙醇为夹带剂,夹带剂质量分数为20%,萃取时间2h,CO2流量为20L/h,产品的出膏率为3.58%,萃取物中熊果酸的含量为6.93%。该法与传统方法相比,具有操作简便快速,溶剂用量少,有效成分提取率高等优点。 相似文献
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超临界CO2萃取β-胡萝卜素的工艺研究 总被引:1,自引:0,他引:1
对超临界CO2萃取胡萝卜中β-胡萝卜素的工艺进行了实验研究.用L9(34)正交实验研究了萃取压力、CO2流量、原料粒径、萃取温度等因素对萃取效果的影响,且对夹带剂的用量进行了研究与探讨.实验结果表明,4个因素中对提取率影响大小依次为压力>流量>粒径>温度,适宜的超临界萃取条件为萃取压力40 MPa,CO2流量10kg·h,原料粒径为40目,萃取温度40℃,此条件下的提取率为30.25×104.夹带剂可明显提高萃取率,适宜的夹带剂添加量为40 mL.此外还将超临界萃取与有机溶剂提取进行了比较,效果均优于有机溶剂. 相似文献
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超临界CO2萃取黑胡椒中有效成分的研究 总被引:2,自引:1,他引:1
用超临界CO2萃取技术,首先在低压、低温的条件下选择性萃取黑胡椒精油,进而在高温、高压及极性夹带剂的协同作用下,萃取富含胡椒碱的黑胡椒油树脂。另外,利用分子蒸馏技术纯化超临界CO2萃取的黑胡椒精油,得到适用于日化行业的无色、无辛辣感的挥发油,并通过GC-MS对比分析其香气成分。研究结果表明,超临界CO2萃取黑胡椒精油的较优条件为:萃取压力10MPa、萃取温度35℃、萃取时间1.5h,在该条件下产物得率为3.01%;超临界CO2萃取黑胡椒油树脂的最佳条件为:m(原料)∶m(体积分数95%食用乙醇)=2∶1、萃取压力30MPa、萃取温度50℃、萃取时间4h,在该条件下油树脂得率为7.88%,油树脂中胡椒碱质量分数为65.79%。 相似文献
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乙烯酮(双乙烯酮)是十分重要的化工中间体,其下游产品较多。江苏某化工厂开发生产乙烯酮(双乙烯酮)下游产品三十多个,年生产规模三万多吨,是国内以乙烯酮(双乙烯酮)为中间体生产精细化学品的综合骨干企业。针对乙烯酮(双乙烯酮)下游产品废水特点,该厂结合企业实际,开展了产品优化,结构调整,清洁生产,资源循环利用,节水降耗等工作,从源头削减了污染物的生产。同时投资二千多万元新建预处理装置三套,6000m3/d废水生化处理装置一套,使全厂乙烯酮(双乙烯酮)下游产品的废水得到了有效的治理。 相似文献
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D. G. Gordeev L. F. Gudarenko M. V. Zhernokletov V. G. Kudel’kin M. A. Mochalov 《Combustion, Explosion, and Shock Waves》2008,44(2):177-189
A semi-empirical equation of state for metals is described. Its capabilities are demonstrated by the example of the equation
of state for aluminum. New experimental data are presented on the location of the isentrope of aluminum for unloading from
the state at p = 229.71 GPa on the shock adiabat to an aerogel (SiO2) of density 0.08 g/cm3.
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Translated from Fizika Goreniya i Vzryva, Vol. 44, No. 2, pp. 61–75, March–April, 2008. 相似文献
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Jorge Marcelo Romero Soledad Bustillo Hugo Enrique Ramirez Maisuls Nelly Lidia Jorge Manuel Eduardo Gómez Vara Eduardo Alberto Castro Alicia H. Jubert 《International journal of molecular sciences》2007,8(7):688-694
A thermochemical rather simple experimental technique is applied to determine the enthalpy of formation of Diperoxide of ciclohexanone. The study is complemented with suitable theoretical calculations at the semiempirical and ab initio levels. A particular satisfactory agreement between both ways is found for the ab initio calculation at the 6–311G basis This set level. Some possible extensions of the present procedure are pointed out. 相似文献
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A perturbation viscometer is a differential capillary viscometer that measures the logarithmic viscosity gradient of the viscosity-composition curve for gas mixtures. Measurements are made at different gas mixture compositions. Integration of the logarithmic viscosity gradients measured over the full composition range gives the mixture viscosity relative to the viscosity of one of the pure components of the gas mixture. This method is attractive because, for measurements of equal precision, integration of the gradients is potentially an order of magnitude more precise than measurement of the viscosities directly. It can also work at high and low temperatures and perhaps high pressures.The perturbation viscometer has been used to make measurements on ideal gas mixtures at ambient and elevated temperatures. The situation is more complicated when the gas mixtures are non-ideal. Extra effects due to density differences, molar volume change on mixing and differential thermal expansion may be measured in addition to the desired viscosity change producing systematic errors in the results. Thus, a more sophisticated apparatus is required. The standard perturbation viscometer has been modified to separate out the extra effects to permit measurement of the true change in viscosity. In addition, the theoretical operation of the modified apparatus has been revised to account for the design changes to permit calculation of the viscosity-composition profiles from the results.The apparatus has been tested using helium-HFC-125 mixtures and two new viscosity-composition profiles are presented for these mixtures at 23 and . Internal consistency tests have been used to confirm that the data produced are of high quality with an estimated uncertainty in the viscosity ratio data at of 0.9% and at of 1.5%. 相似文献
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醋酸纤维素取代基分布与性质的关系 总被引:9,自引:0,他引:9
分析了以吡啶为溶剂的醋酸纤维素的13C-NMR核磁共振谱,得出了三种不同位置羟基的取代度。结合X—射线和DSC分析,初步说明具有相同取代度但未经水解和经过水解的醋酸纤维素(CA) 性质上的差异是由于三个羟基上的取代度分布不同及消晶程度差异所致。 相似文献