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利用提升管催化裂解实验装置研究了加拿大合成原油瓦斯油HGO和LGO的催化裂解反应规律和裂解产品性质。发现总低碳烯烃(乙烯、丙烯和丁烯)产率随反应温度和剂油比的增大存在最大值,随反应时间的延长而减小,随水油比的增大而升高。实验确定了HGO催化裂解的优化反应条件:反应温度620~640℃、剂油比16、反应时间2 s、水油比0.5左右。在此反应条件下,乙烯、丙烯和总低碳烯烃产率分别可达9.0%(质量),15.8%(质量)和32.6%(质量)。催化裂解汽油馏分、柴油馏分和重油馏分含有大量的芳香烃,其中催化裂解汽油馏分总芳香烃含量在80%(质量)以上,主要是甲苯和C8芳香烃;催化裂解柴油馏分总芳香烃含量在60%(质量)以上,主要是单环和双环芳香烃;催化裂解重油馏分总芳香烃含量在70%(质量)以上,主要是多环芳香烃。 相似文献
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反应温度对汽油催化裂解多产低碳烯烃的影响 总被引:1,自引:0,他引:1
利用自制的多产低碳烯烃催化剂在小型固定流化床装置上对催化裂化汽油、焦化汽油和直馏汽油的催化裂解性能进行了实验研究,考察了反应温度对催化裂解产物分布和低碳烃收率的影响.实验结果表明焦化汽油、催化汽油和直馏汽油最佳的催化裂解反应温度分别为580、600℃和680℃,随着反应物活性的降低而显著增加.乙烯的收率随着反应温度的升高呈抛物线增长;烯烃与正构烷烃有协同反应作用,烯烃能够加速正构链烷烃的反应速率;在烯烃存在下,芳烃会生成大量的焦炭;烯烃和链烷烃是生成低碳烯烃的主要来源,是催化裂解的理想组分;最佳催化裂解的反应物为催化汽油或者焦化汽油的轻馏分与直馏汽油的轻馏分的混合物. 相似文献
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分别以软蜡裂解全馏分C5~C15轻烯烃、软蜡裂解窄馏分C8~C12轻烯烃、58号半精蜡裂解全馏分轻烯烃为原料,在实验室合成了润滑油基础油,比较了产品的性能,研究了不同馏分烯烃原料对润滑油基础油性能的影响. 相似文献
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从裂解碳四馏分或丁烯氧化脱氢馏分中萃取丁二烯,目前国内采用的萃取剂有二甲基甲酰胶和乙腈两种。关于二甲基甲酰胺及其副产物二甲胺对镍体系催化聚合丁二烯的影响,前报已介绍,本文将报导乙腈及其水解生成物氨对该体系的影响。 相似文献
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介绍了以溶剂油为载热体的甲基氯硅烷水解物裂解技术原理、工艺流程、产业化过程和效果.通过用溶剂油为载热体进行水解物裂解及混合环硅氧烷精馏,生产出聚合物中间体八甲基环四硅氧烷(D4),该产品用于合成高温硫化硅橡胶、室温硫化硅橡胶、硅油等. 相似文献
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Summary A study was made of the degree of splitting of coconut and soybean oils by the Twitchell process at 35±0.1°C. with no shaking
or stirring, using an agent consisting mainly of tetrabutyl naphthalene sulfonic acid with water or dilute sulfuric acid.
The degree of splitting was greater with sulfuric acid than with water. In general, the degree of splitting of soybean oil
was greater when the sulfonic acid was dissolved in the oil layer than when it was in water. The reverse was true with coconut
oil. Although addition of glycerol had no effect on the degree of splitting, addition of glacial acetic acid to the coconut
oil system decreased fat splitting to a considerable extent. Addition of coconut fatty acids to the coconut oil system had
little effect, but soybean fatty acids added to the soybean oil system markedly increased the degree of splitting.
For the first time it has been demonstrated that, at 35±0.1°C., splitting of a fat by the Twitchell process occurs in a stepwise
way. Coconut oil in contact with 1N sulfuric acid containing the sulfonic acid, corresponding to 1% by the weight of the oil, was about 90% split in 15 to 30
days, depending on the area of contact of the two layers. The diglyceride concentration reached a maximum during the early
days of the reaction and then decreased somewhat. Monoglyceride concentration appeared to reach a maximum more slowly and
then continued at that level as the concentrations of free fatty acids and glycerol steadily increased.
Presented at the symposia on fat of the Chemical Society of Japan, Nov. 10, 1954, and Nov. 8, 1955, Nagoya, Japan; and the
8th annual meeting of the Chemical Society of Japan, Apr. 2, 1955, Tokyo, Japan. 相似文献
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Chung Gi Baig Young Ho Chun Eun Su Cho Chang Kyun Choi 《Korean Journal of Chemical Engineering》2000,17(2):169-173
When air is injected into silicone oil contained in a horizontal Hele-Shaw cell, a single air bubble forms and grows showing
various interesting phenomena. In this study the effects of the bubble front velocity, air injection velocity at a nozzle,
fluid properties and cell depth on the stability of the growing bubble were investigated experimentally. By using the modified
capillary number involving the aspect ratio, we obtained the onset conditions of the unstable bubble. Also, the bubble width
was analyzed both quantitatively and qualitatively. Before the bubble experiences splitting, the bubble front velocity is
almost proportional to the air injection velocity. Therefore the latter velocity may be used in a practical sense. 相似文献
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Seiichi Deguchi Toshinori Takeichi Shoji Shimasaki Muneaki Ogawa Norifumi Isu 《American Institute of Chemical Engineers》2011,57(8):2237-2243
To enhance photocatalytic water splitting, various oxidizing sacrifice agents (OSA) have been added to the system in order to scavenge the coproduced O2, and, thus, to hinder the reverse reactions. In the aim of achieving carbon‐neutral photocatalytic water splitting, nonfood hydrocarbons of castor‐ and jojoba‐oils were evaluated as OSA. Moreover, various surfactants were tested as emulsifiers for W/O binary solution for promoting photocatalytic water splitting rate. Among the OSA used, the castor‐oil was found to be more suitable candidate compared to jojoba‐oil, which was attributed to its smaller carbon chain numbers of mainly 18. Without surfactants, around 20 vol %‐castor‐oil aqueous binary solution with TiO2/Pt(0.10 wt %) provided the highest water splitting rate of about 30 mL‐H2/(m2·h). Among tested surfactants, liquid‐detergent was the best due to its optical transparency. 40 vol %‐ or 60 vol %‐castor‐oil emulsion with a drop of liquid‐detergent resulted in a water splitting rate of 125 mL‐H2/(m2·h), which was four times greater that the aforementioned highest value. © 2010 American Institute of Chemical Engineers AIChE J, 2011 相似文献
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Characteristics of emulsion formation and splitting into aqueous and oily phases in simple and formulated surfactant systems
were studied via conductivity. In systems composed of mixed nonionic ethoxylated alcohol surfactants, K2CO3, and emulsified n-hexadecane, conductivity decreased linearly with increasing oil volume fraction at HLB (hydrophile-lipophile balance) values
of 12.9 and 13.9. The slope of the plot was ca. −3/2, in agreement with the Maxwell expression. At values less than or equal to an HLB of 11.3, conductivity first increased
with a small addition of oil and then decreased nearly linearly with subsequent amounts. This was probably due to low HLB
surfactants partitioning into the oily phase. When the type of oil was varied, the reduced conductivity also decreased linearly
with volume fraction of emulsified oil. The slope was ca. −3/2 for oil weights ranging from very light (n-hexadecane) to very heavy (80W–90 gear oil), also in agreement with the Maxwell expression. Oil separation rates were measured
by monitoring the change in conductivity in the lower region of the emulsion (where the aqueous layer formed) during splitting
of the oily phase. Heavier oils were found to separate faster than light oils. Oils containing lubricity agents split at the
slowest rate. Systems with lower HLB surfactants also displayed slower splitting rates. Splitting rates for a variety of systems,
from simple oil and saline systems to more complex formulated systems, over temperatures from 23 to 75°C, were related to
oil-aqueous interfacial tension values through a power law expression composed of the maximum splitting rate and the interfacial
tension between saline and oil at 23°C. 相似文献
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Process Experiences with a Stream Gas Washer for Soap Splitting Procedure and process data for a stream gas washer with superposed cocondenser for cooling and desodorization of vapours from soap splitting are reported. The plant treats vapours from splitting of about 250 m3 soap solution a day (soapstock of palm oil, coconut oil, liquid oils and hardened fats). The exhaust air, treated with water and oxidation chemicals is nearly free of acids and odourless purified. 相似文献
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Soap Splitting – Continuous and Ecologically Harmless In the classical refining of vegetable oils the free fatty acids are saponified and separated from oil by centrifuging. The centrifuged soap solution also contains neutral oil and non hydrationable sliming substances. The resulting emulsion impedes splitting and the separation of the aqueous phase from the oily fatty acid phase. Therefore you often work with high surplus of sulphuric acid and direct vapour for heating and stirring. The direct vapour carries away fatty acid and sulphuric acid as aerosol and must be washed before drawing out into the enviroment. If the mixture from the centrifuges undergoes a saponification reaction, splitting can be continuously carried out by addition of sulphuric acid, regulated by the pH-value, without direct vapour. Thus an important requirement for an ecologically harmless procedure of soap splitting is given. 相似文献