CN104498078B - The method of crude oil or heavy crude intensifying distillation - Google Patents
The method of crude oil or heavy crude intensifying distillation Download PDFInfo
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- CN104498078B CN104498078B CN201410817965.XA CN201410817965A CN104498078B CN 104498078 B CN104498078 B CN 104498078B CN 201410817965 A CN201410817965 A CN 201410817965A CN 104498078 B CN104498078 B CN 104498078B
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- 239000010779 crude oil Substances 0.000 title claims abstract description 60
- 238000004821 distillation Methods 0.000 title claims abstract description 30
- 238000000034 method Methods 0.000 title claims abstract description 18
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- 108090001061 Insulin Proteins 0.000 claims abstract description 23
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims abstract description 18
- 238000002203 pretreatment Methods 0.000 claims abstract description 14
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims abstract description 9
- 235000017557 sodium bicarbonate Nutrition 0.000 claims abstract description 9
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- 238000003756 stirring Methods 0.000 claims description 73
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- RUDATBOHQWOJDD-UZVSRGJWSA-N ursodeoxycholic acid Chemical compound C([C@H]1C[C@@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)CC1 RUDATBOHQWOJDD-UZVSRGJWSA-N 0.000 claims description 6
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- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical compound C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 claims description 4
- 239000003613 bile acid Substances 0.000 claims description 4
- KXGVEGMKQFWNSR-LLQZFEROSA-N deoxycholic acid Chemical compound C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 KXGVEGMKQFWNSR-LLQZFEROSA-N 0.000 claims description 4
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- RFDAIACWWDREDC-FRVQLJSFSA-N glycocholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 RFDAIACWWDREDC-FRVQLJSFSA-N 0.000 claims description 2
- DGABKXLVXPYZII-SIBKNCMHSA-N hyodeoxycholic acid Chemical compound C([C@H]1[C@@H](O)C2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)CC1 DGABKXLVXPYZII-SIBKNCMHSA-N 0.000 claims description 2
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- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 claims 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G7/00—Distillation of hydrocarbon oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G7/00—Distillation of hydrocarbon oils
- C10G7/12—Controlling or regulating
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1037—Hydrocarbon fractions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/40—Characteristics of the process deviating from typical ways of processing
- C10G2300/4006—Temperature
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Steroid Compounds (AREA)
Abstract
Description
技术领域technical field
本发明涉及原油或重质原油强化蒸馏的方法。The invention relates to a method for enhanced distillation of crude oil or heavy crude oil.
背景技术Background technique
目前,我国加工的原油日趋重质化,劣质化。我国的原油成分与国外原油成分相比,其减压渣油含量较高,多数油田的原油中减压渣油的质量高达40%-50%。特别是老油田,不仅产量在递减,而且原油的重质化倾向加剧。除此之外,我国原油对外依赖程度较高,已达75%,而且重质化比例也日渐加激。因此,研发原油,特别是重质原油的强化蒸馏技术改进重油或重质原油的深度加工,充分利用有限的石油资源,增加轻质油的产量,提高经济效益,已成为我国石油炼化工业迫切需要解决的问题,也是现代原油或重质原油蒸馏技术进步和发展的重要方向。At present, my country's processed crude oil is becoming increasingly heavy and inferior. Compared with foreign crude oil components, my country's crude oil composition has a higher vacuum residue content, and the quality of vacuum residue in crude oil in most oil fields is as high as 40%-50%. Especially in old oilfields, not only is the output declining, but the crude oil tends to become heavier. In addition, my country's dependence on foreign crude oil is relatively high, reaching 75%, and the proportion of heavy crude oil is also increasing day by day. Therefore, research and development of crude oil, especially the enhanced distillation technology of heavy crude oil to improve the deep processing of heavy oil or heavy crude oil, make full use of limited oil resources, increase the output of light oil, and improve economic benefits have become an urgent need for my country's petroleum refining and chemical industry. The problem to be solved is also an important direction for the progress and development of modern crude oil or heavy crude oil distillation technology.
在强化剂强化原油蒸馏方面,如俄罗斯新乌发炼油厂用减三线精制抽出油与重油混合进行减压蒸馏,其拔出率增加4.3%。在西西伯利亚原油中加入C12-C14高级脂肪醇4%-5%时,轻质馏分油的收率最佳。我国在强化剂方面,采用如催化裂化油浆、苯酚、活化剂NO.3,以及一些复合添加剂等,都在一定程度上能提高VGO的拔出率。In terms of enhanced crude oil distillation with enhancers, for example, Russia's Xinwufa Oil Refinery used the third-line refined extraction oil to mix with heavy oil for vacuum distillation, and the extraction rate increased by 4.3%. When 4%-5% of C12-C14 higher fatty alcohol is added to West Siberia crude oil, the yield of light distillate oil is the best. In terms of strengthening agents in my country, such as catalytic cracking oil slurry, phenol, activator NO.3, and some compound additives, etc., can improve the pull-out rate of VGO to a certain extent.
发明内容Contents of the invention
本发明要解决的技术问题是提供一种常压蒸馏反应条件温和、绿色环保、增加气液收率、清澈透明的浅黄色轻组分收率显著、能使颜色变化的转折温度升高和刺激气味出现的温度延后、工艺简单、操作方便易行的原油或重质原油强化蒸馏的方法。The technical problem to be solved by the present invention is to provide a kind of atmospheric distillation with mild reaction conditions, environmental protection, increased gas-liquid yield, clear and transparent light yellow light component yield is remarkable, and can increase the transition temperature of color change and stimulate A method for enhanced distillation of crude oil or heavy crude oil with delayed temperature for odor appearance, simple process, and convenient operation.
为解决上述技术问题本发明采用如下技术方案:In order to solve the problems of the technologies described above, the present invention adopts the following technical solutions:
原油或重质原油强化蒸馏的方法,包括以下步骤:A method for enhanced distillation of crude oil or heavy crude oil, comprising the following steps:
<1>利用生物质油对原油或重质原油进行预处理:常温下把生物质油和原油或重质原油混合并于36.5-38℃恒温磁力搅拌均匀,生物质油的添加量为原油体积的0.5%-10%;<1> Use biomass oil to pretreat crude oil or heavy crude oil: mix biomass oil and crude oil or heavy crude oil at room temperature and stir evenly at a constant temperature of 36.5-38 ° C, and the amount of biomass oil added is the volume of crude oil 0.5%-10%;
<2>二次预处理:把胆酸类活化剂加入进步骤<1>所得的混合物中,添加量为0.01-0.05mg/g,并于36.5℃-38℃恒温磁力搅拌均匀;然后在36.5℃-38℃恒温水浴加热3-6小时;<2>Secondary pretreatment: add the bile acid activator into the mixture obtained in step <1>, the addition amount is 0.01-0.05mg/g, and stir evenly at a constant temperature of 36.5°C-38°C; ℃-38℃ constant temperature water bath heating for 3-6 hours;
<3>三次预处理:把胰岛素添加进步骤<2>所得的混合物中,并于36.5℃-38℃恒温磁力搅拌均匀;然后在36℃-38℃恒温水浴加热3-24小时;<3>Three pretreatments: add insulin to the mixture obtained in step <2>, and stir evenly at a constant temperature of 36.5°C-38°C; then heat in a constant temperature water bath at 36°C-38°C for 3-24 hours;
<4>四次预处理:步骤<3>所得混合物中添加小苏打或大苏打进行再次预处理,添加量为0.05-0.10mg/g,并于36.5℃-38℃恒温磁力搅拌均匀;<4>Four times of pretreatment: add baking soda or sodium bicarbonate to the mixture obtained in step <3> for another pretreatment, the addition amount is 0.05-0.10mg/g, and stir evenly at a constant temperature of 36.5°C-38°C;
<5>把经步骤<4>预处理的混合物,进行常压蒸馏。<5> carry out normal pressure distillation through step <4> pretreated mixture.
所述步骤<1>中的生物质油是松节油、蓖麻油、桐油、棕榈油、大豆油、葵花籽油、油菜籽油、花生油或玉米坯芽油。The biomass oil in the step <1> is turpentine oil, castor oil, tung oil, palm oil, soybean oil, sunflower oil, rapeseed oil, peanut oil or corn cocoa germ oil.
所述步骤(1)中搅拌转速为50rpm-100rpm,搅拌时间0.5-1小时。In the step (1), the stirring speed is 50rpm-100rpm, and the stirring time is 0.5-1 hour.
所述胆酸类活化剂为胆酸、胆酸钠、胆酸盐、去氧胆酸盐、熊去氧胆酸片、熊去氧胆酸胶囊、熊去氧胆酸软胶囊、脱氧胆酸、猪去氧胆酸或甘氨胆酸。The bile acid activator is cholic acid, sodium cholate, cholate, deoxycholic acid salt, ursodeoxycholic acid tablet, ursodeoxycholic acid capsule, ursodeoxycholic acid soft capsule, deoxycholic acid, Hyodeoxycholic acid or glycocholic acid.
所述步骤(2)中搅拌转速是50rpm-100rpm,搅拌时间1-2小时。In the step (2), the stirring speed is 50rpm-100rpm, and the stirring time is 1-2 hours.
所述步骤<3>中的胰岛素是注射用粉针剂胰岛素或注射剂状胰岛素;注射用粉针剂胰岛素的添加量为0.01—0.10mg/ml;注射剂状胰岛素的添加量为0.05—0.2ml/ml,添加注射剂状胰岛素的原油在蒸馏前去除其所携带的水分。The insulin in the step <3> is insulin powder for injection or insulin for injection; the amount of insulin for injection powder is 0.01-0.10mg/ml; the amount of insulin for injection is 0.05-0.2ml/ml, Crude oil to which injectable insulin is added is distilled to remove its entrained water.
所述步骤<3>中搅拌转速是50rpm-100rpm,搅拌时间1-3小时。In the step <3>, the stirring speed is 50rpm-100rpm, and the stirring time is 1-3 hours.
所述步骤<4>中搅拌转速是50rpm-100rpm,搅拌时间为0.5-1小时。与现有技术相比,本发明的优点在于:In the step <4>, the stirring speed is 50rpm-100rpm, and the stirring time is 0.5-1 hour. Compared with the prior art, the present invention has the advantages of:
1.工艺简单,操作简便易行。1. The process is simple and the operation is simple and easy.
2.该方法应用于原油或重质原油的常压蒸馏反应条件温和,绿色环保,气液收率增加明显,清澈透明的浅黄色轻组分收率增加显著,而且与空白或仅添加胆酸或仅添加胰岛素时相比,该轻组分更为清澈、粘度更低。2. This method is applied to the atmospheric distillation of crude oil or heavy crude oil. The reaction conditions are mild, green and environmentally friendly, the gas-liquid yield increases significantly, and the yield of clear and transparent light yellow light components increases significantly. This light fraction is clearer and less viscous than when insulin alone is added.
3.颜色变化的转折温度升高了30℃-55℃,295℃以后,温度上升开始变慢,并有极轻微刺激性气味出现;当温度到达320℃-335℃,颜色慢慢开始变棕色,刺激性气味一直较浅。刺激气味出现的温度比空白试验刺激气味出现的温度延后了35℃-55℃,同时,伴随有爆裂的响声出现,说明此时,原油开始裂化,比仅添加胆酸类活化剂时裂化温度升高了20℃-35℃。3. The transition temperature of the color change increased by 30°C-55°C. After 295°C, the temperature rise began to slow down, and a very slight pungent smell appeared; when the temperature reached 320°C-335°C, the color slowly began to turn brown , The pungent smell has always been light. The temperature at which the irritating odor appeared was 35°C-55°C later than that of the blank test, and at the same time, there was a popping sound, indicating that at this time, the crude oil began to crack, which was higher than the cracking temperature when only bile acid activators were added. Increased by 20°C-35°C.
具体实施方式:detailed description:
以下结合实施例对本发明作进一步的说明,但不构成对本发明保护范围的限制。The present invention will be further described below in conjunction with the examples, but it is not intended to limit the protection scope of the present invention.
实施例1:Example 1:
常温下把添加量为原油体积0.5%松节油和100ml的原油均匀混合,并用恒温磁力搅拌器在36.5℃搅拌均匀,搅拌时的转速是:50rpm,搅拌持续时间为:0.5小时;二次预处理:把胆酸按质量体积浓度0.01mg/g添加到上述混合物中,并用恒温磁力搅拌器在36.5℃搅拌均匀,搅拌转速是:50rpm,搅拌持续时间为1小时;然后在36.5℃恒温水浴加热3小时;三次预处理:注射用粉针剂胰岛素按0.01mg/ml添加进上述混合物中,再用恒温磁力搅拌器在36.5℃搅拌均匀,搅拌转速是:50rpm,搅拌持续时间为1小时;然后在36.5℃恒温水浴加热反应3小时;四次预处理:添加大苏打进行再次预处理,添加量为0.05mg/g,并用恒温磁力搅拌器在36.5℃搅拌均匀,搅拌转速是:50rpm,搅拌持续时间为:0.5小时;最后,把经上述预处理好的混合物,进行常压蒸馏,此时,轻组分出现淡棕色的温度升为315℃,颜色变化的转折温度升高了30℃;有轻微刺激气味出现的温度为320℃,刺激气味出现的温度延后了35℃。在蒸馏温度达到345-350℃下的气液收率为62.5ml,其气液收率比空白时增加了68.9%。At room temperature, evenly mix turpentine with an amount of 0.5% of crude oil volume and 100ml of crude oil, and stir evenly with a constant temperature magnetic stirrer at 36.5°C. The rotation speed during stirring is: 50rpm, and the duration of stirring is: 0.5 hours; Secondary pretreatment: Add cholic acid to the above mixture at a mass volume concentration of 0.01mg/g, and stir evenly with a constant temperature magnetic stirrer at 36.5°C, the stirring speed is: 50rpm, and the stirring duration is 1 hour; then heat in a constant temperature water bath at 36.5°C for 3 hours ;Three pretreatments: Add insulin powder for injection into the above mixture at 0.01mg/ml, then stir evenly with a constant temperature magnetic stirrer at 36.5°C, the stirring speed is: 50rpm, and the stirring duration is 1 hour; then stir at 36.5°C Heating and reacting in a constant temperature water bath for 3 hours; four pretreatments: add sodium bicarbonate for pretreatment again, the addition amount is 0.05mg/g, and stir evenly with a constant temperature magnetic stirrer at 36.5°C, the stirring speed is: 50rpm, and the stirring duration is: 0.5 hours; finally, carry out normal pressure distillation on the above-mentioned pretreated mixture, at this time, the light brown temperature of the light component rises to 315°C, and the turning temperature of the color change increases by 30°C; there is a slight pungent smell The onset temperature was 320°C, and the onset of the pungent odor was delayed by 35°C. When the distillation temperature reaches 345-350°C, the gas-liquid yield is 62.5ml, which is 68.9% higher than that of the blank.
实施例2:Example 2:
常温下把添加量为原油体积4.0%蓖麻油和100ml的原油均匀混合,并用恒温磁力搅拌器在37℃搅拌均匀,搅拌转速是:60rpm,搅拌持续时间为:0.6小时;二次预处理:把胆酸钠按质量体积浓度为0.02mg/g添加到上述混合物中,并用恒温磁力搅拌器在37℃搅拌均匀,搅拌转速是:60rpm,搅拌持续时间为:1.2小时;然后在37℃恒温水浴加热4小时;三次预处理:注射用粉针剂胰岛素按0.05mg/ml添加进上述混合物中,再用恒温磁力搅拌器在37℃搅拌均匀,搅拌转速是:60rpm,搅拌持续时间为:1.5小时;然后在37℃恒温水浴加热10小时;四次预处理:添加大苏打进行再次预处理,添加量为0.07mg/g,并用恒温磁力搅拌器在37℃搅拌均匀,搅拌转速是:60rpm,搅拌持续时间为:0.6小时;最后,把经上述预处理好的混合物,进行常压蒸馏,此时,轻组分出现淡棕色的温度升为320℃,颜色变化的转折温度升高了35℃;有轻微刺激气味出现的温度为325℃,刺激气味出现的温度延后了40℃。在蒸馏温度达到345-350℃下的气液收率为67.6ml,其气液收率比空白时增加了82.7%以上。At room temperature, mix the castor oil with an amount of 4.0% of crude oil volume and 100ml of crude oil evenly, and stir evenly at 37°C with a constant temperature magnetic stirrer, the stirring speed is: 60rpm, and the stirring duration is: 0.6 hours; the second pretreatment: put Add sodium cholate to the above mixture according to the mass volume concentration of 0.02mg/g, and stir evenly with a constant temperature magnetic stirrer at 37°C, the stirring speed is: 60rpm, and the stirring duration is: 1.2 hours; then heat in a constant temperature water bath at 37°C 4 hours; three pretreatments: Add insulin powder for injection to the above mixture at 0.05mg/ml, then stir evenly with a constant temperature magnetic stirrer at 37°C, the stirring speed is: 60rpm, and the stirring duration is: 1.5 hours; then Heating in a constant temperature water bath at 37°C for 10 hours; four pretreatments: add sodium bicarbonate for pretreatment again, the addition amount is 0.07mg/g, and stir evenly at 37°C with a constant temperature magnetic stirrer, the stirring speed is: 60rpm, the duration of stirring For: 0.6 hours; finally, carry out normal pressure distillation to the above-mentioned pretreated mixture, at this time, the temperature at which the light component appears light brown rises to 320°C, and the transition temperature of the color change increases by 35°C; there is a slight The temperature at which the irritating odor appeared was 325°C, and the temperature at which the irritating odor appeared was delayed by 40°C. When the distillation temperature reaches 345-350°C, the gas-liquid yield is 67.6ml, which is more than 82.7% higher than that of the blank.
实施例3:Embodiment 3:
常温下把添加量为原油体积8.0%桐油和100ml的重质原油均匀混合,并用恒温磁力搅拌器在37.5℃搅拌均匀,搅拌转速是:70rpm,搅拌持续时间为:0.8小时;二次预处理:把胆酸盐按质量体积浓度为0.04mg/g添加到上述混合物中,并用恒温磁力搅拌器在37.5℃搅拌均匀,搅拌转速是:70rpm,搅拌持续时间为:1.5小时;然后在37.5℃恒温水浴加热5小时;三次预处理:注射剂状胰岛素按0.07ml/ml添加进上述混合物中,该胰岛素的品牌规格是:诺和灵30R精蛋白生物合成人胰岛素注射液400IU/10ml/支;再用恒温磁力搅拌器在37℃搅拌均匀,搅拌转速是:70rpm,搅拌持续时间为:2.0小时;然后在37.5℃恒温水浴加热20小时;此间,不间断更换试管口的脱脂棉,以尽可能去除胰岛素注射液中所携带的水分;四次预处理:添加小苏打进行再次预处理,添加量为0.08mg/g,并用恒温磁力搅拌器在37.5℃搅拌均匀,搅拌转速是:80rpm,搅拌持续时间为:0.8小时;最后,把经上述预处理好的混合物,进行常压蒸馏,此时,轻组分出现淡棕色的温度升为330℃,颜色变化的转折温度升高了45℃;有轻微刺激气味出现的温度为335℃,刺激气味出现的温度延后了50℃。在蒸馏温度达到345-350℃下的气液收率为70.8ml,其气液收率比空白时增加了91.4%以上。At room temperature, mix tung oil with 8.0% volume of crude oil and 100ml of heavy crude oil evenly, and stir evenly with a constant temperature magnetic stirrer at 37.5°C, stirring speed: 70rpm, stirring duration: 0.8 hours; secondary pretreatment: Add cholate to the above mixture at a mass volume concentration of 0.04mg/g, and stir evenly at 37.5°C with a constant temperature magnetic stirrer, the stirring speed is: 70rpm, and the stirring duration is: 1.5 hours; then in a constant temperature water bath at 37.5°C Heating for 5 hours; three pretreatments: Injection-like insulin was added to the above mixture at 0.07ml/ml. The brand specification of the insulin was: Novolin 30R Protamine Biosynthetic Human Insulin Injection 400IU/10ml/branch; Stir evenly with a magnetic stirrer at 37°C, stirring speed: 70rpm, stirring duration: 2.0 hours; then heat in a constant temperature water bath at 37.5°C for 20 hours; during this time, continuously replace the absorbent cotton at the test tube mouth to remove insulin injection as much as possible Moisture carried in the water; four pretreatments: Add baking soda for pretreatment again, the addition amount is 0.08mg/g, and stir evenly with a constant temperature magnetic stirrer at 37.5°C, the stirring speed is: 80rpm, and the stirring duration is: 0.8 Hours; finally, carry out normal pressure distillation on the above-mentioned pretreated mixture, at this time, the temperature at which the light component appears light brown rises to 330°C, and the transition temperature of the color change increases by 45°C; a slight pungent odor appears The temperature of the test was 335°C, and the temperature at which the pungent odor appeared was delayed by 50°C. When the distillation temperature reaches 345-350°C, the gas-liquid yield is 70.8ml, which is more than 91.4% higher than that of the blank.
实施例4:Example 4:
常温下把添加量为原油体积10.0%棕榈油和100ml的重质原油均匀混合,并用恒温磁力搅拌器在38℃搅拌均匀,搅拌转速是:100rpm,搅拌持续时间为:1.0小时;二次预处理:把胆酸按质量体积浓度为0.05mg/g添加到上述混合物中,并用恒温磁力搅拌器在38℃搅拌均匀,搅拌转速是:100rpm,搅拌持续时间为:2.0小时;然后在38℃恒温水浴加热6小时;三次预处理:注射用粉针剂胰岛素按0.10mg/ml添加进上述混合物中,再用恒温磁力搅拌器在38℃搅拌均匀,搅拌转速是:100rpm,搅拌持续时间为:3.0小时;然后38℃恒温水浴加热24小时;四次预处理:添加小苏打进行再次预处理,添加量为0.10mg/g,并用恒温磁力搅拌器在38℃搅拌均匀,搅拌转速是:100rpm,搅拌持续时间为:1.0小时;最后,把经上述预处理好的混合物,进行常压蒸馏,此时,轻组分出现淡棕色的温度升为335℃,颜色变化的转折温度升高了50℃;有轻微刺激气味出现的温度为345℃,刺激气味出现的温度延后了55℃。在蒸馏温度达到345-350℃下的气液收率为73.6ml,其气液收率比空白时增加了98.9%以上。At room temperature, evenly mix palm oil and 100ml of heavy crude oil in an amount of crude oil volume of 10.0%, and stir evenly with a constant temperature magnetic stirrer at 38°C. The stirring speed is: 100rpm, and the stirring duration is: 1.0 hours; secondary pretreatment : Add cholic acid to the above mixture according to the mass volume concentration of 0.05mg/g, and stir evenly at 38°C with a constant temperature magnetic stirrer, the stirring speed is: 100rpm, and the stirring duration is: 2.0 hours; then in a constant temperature water bath at 38°C Heating for 6 hours; three pretreatments: Add insulin powder for injection to the above mixture at 0.10 mg/ml, then stir evenly with a constant temperature magnetic stirrer at 38°C, stirring speed: 100rpm, stirring duration: 3.0 hours; Then heat in a constant temperature water bath at 38°C for 24 hours; four pretreatments: add baking soda for pretreatment again, the addition amount is 0.10mg/g, and stir evenly at 38°C with a constant temperature magnetic stirrer, the stirring speed is: 100rpm, the duration of stirring For: 1.0 hour; Finally, carry out normal pressure distillation to the above-mentioned pretreated mixture, at this moment, the temperature at which the light component appears light brown rises to 335°C, and the transition temperature of the color change increases by 50°C; there is a slight The temperature at which the pungent odor appeared was 345°C, and the temperature at which the pungent odor appeared was delayed by 55°C. When the distillation temperature reaches 345-350°C, the gas-liquid yield is 73.6ml, which is more than 98.9% higher than that of the blank.
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