JP2010111771A - Method for producing purified hydrocarbon oil, and purified hydrocarbon oil - Google Patents

Method for producing purified hydrocarbon oil, and purified hydrocarbon oil Download PDF

Info

Publication number
JP2010111771A
JP2010111771A JP2008285642A JP2008285642A JP2010111771A JP 2010111771 A JP2010111771 A JP 2010111771A JP 2008285642 A JP2008285642 A JP 2008285642A JP 2008285642 A JP2008285642 A JP 2008285642A JP 2010111771 A JP2010111771 A JP 2010111771A
Authority
JP
Japan
Prior art keywords
fraction
hydrocarbon oil
oil
refined
boiling point
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2008285642A
Other languages
Japanese (ja)
Inventor
Masanari Minatoya
昌成 港谷
Yosuke Koakutsu
陽介 小圷
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SEKIYU COMBINAT KODO TOGO UNEI
Research Association of Refinery Integration for Group Operation
Eneos Corp
Original Assignee
SEKIYU COMBINAT KODO TOGO UNEI
Japan Energy Corp
Research Association of Refinery Integration for Group Operation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SEKIYU COMBINAT KODO TOGO UNEI, Japan Energy Corp, Research Association of Refinery Integration for Group Operation filed Critical SEKIYU COMBINAT KODO TOGO UNEI
Priority to JP2008285642A priority Critical patent/JP2010111771A/en
Publication of JP2010111771A publication Critical patent/JP2010111771A/en
Pending legal-status Critical Current

Links

Images

Landscapes

  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for producing purified hydrocarbon oil, in which when a sulfur content in hydrocarbon oil having specific properties as crude is reduced by hydrotreating to obtain purified hydrocarbon oil, a fraction having a reduced content of bi- and higher-cyclic aromatic hydrocarbon compounds and a boiling point range of 150-250°C can be obtained. <P>SOLUTION: The method for producing purified hydrocarbon oil comprises hydrotreating hydrocarbon oil having such distillation properties as a 10 vol.% distillation temperature of 35-80°C and a 97 vol.% distillation temperature of 250-420°C, having a proportion of a fraction having a boiling point range of 150 to <250°C within a range of 20-35 vol.%, and satisfying the relationships of S1>S2 and S1>S3, wherein S1 represents a sulfur content in a fraction having a boiling point range of 30 to <150°C; S2 represents a sulfur content in a fraction having a boiling point range of 150 to <250°C; and S3 represents a sulfur content in a fraction having a boiling point range of 250 to <350°C. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

本発明は、精製炭化水素油の製造方法および該製造方法を用いて製造した精製炭化水素油に関し、特には、特定の性状を有する炭化水素油を原料として、水素化精製処理により炭化水素油中の硫黄分を低減して精製炭化水素油とする際に、二環以上の芳香族炭化水素化合物の含有量を低減した沸点範囲が150〜250℃の留分を含有する留分を得ることが可能な精製炭化水素油の製造方法および該製造方法を用いて製造した精製炭化水素油に関するものである。   The present invention relates to a method for producing a refined hydrocarbon oil and a refined hydrocarbon oil produced by using the method, and in particular, a hydrocarbon oil having a specific property as a raw material to be used in a hydrocarbon oil by hydrorefining treatment. A refined hydrocarbon oil by reducing the sulfur content of the product, it is possible to obtain a fraction containing a fraction having a boiling point range of 150 to 250 ° C. with a reduced content of bicyclic or higher aromatic hydrocarbon compounds. The present invention relates to a method for producing a possible refined hydrocarbon oil and a refined hydrocarbon oil produced using the production method.

従来の原油の精製処理においては、図1に示すように、原油を常圧蒸留装置1により常圧蒸留して、軽質ガス、LPガス、ナフサ(軽質ナフサ、重質ナフサ)、灯油、軽油及び残油のそれぞれの留分に分離している。そして、常圧蒸留後、軽質ガスは、アミン精製装置2で酸性ガスを分離されて燃料ガスとなり、一方、軽質ガスから分離された酸性ガスは、硫黄回収装置3に送られ、該酸性ガスから硫黄が回収される。また、分離されたLPガスは、LPガス処理装置4で不純物を除去した後、製品LPガスとされる。   In the conventional refining process of crude oil, as shown in FIG. 1, crude oil is distilled at atmospheric pressure by an atmospheric distillation apparatus 1 to obtain light gas, LP gas, naphtha (light naphtha, heavy naphtha), kerosene, light oil and Separated into each fraction of residual oil. Then, after atmospheric distillation, the light gas is separated from the acid gas by the amine purifier 2 to become a fuel gas, while the acid gas separated from the light gas is sent to the sulfur recovery device 3 from the acid gas. Sulfur is recovered. Further, the separated LP gas is made into product LP gas after impurities are removed by the LP gas processing device 4.

また、軽質ナフサ留分は、軽質ナフサ処理装置5にて簡単な処理を施されて、ガソリンや石化原料となり、重質ナフサ留分は、水素化精製装置6において触媒存在下で水素化精製処理された後、接触改質装置7で、異性化や芳香族化されてガソリンや芳香族製品となる。なお、常圧蒸留装置1からナフサ留分を一括で留出させた後、全ナフサ留分をナフサ用の水素化精製装置8において触媒存在下で水素化精製処理し、その後に軽質ナフサ及び重質ナフサに分離することもある。   The light naphtha fraction is subjected to a simple treatment in the light naphtha treatment device 5 to become gasoline or a petrochemical raw material. The heavy naphtha fraction is hydrorefined in the hydrorefining device 6 in the presence of a catalyst. Then, it is isomerized or aromatized by the catalytic reforming device 7 to become gasoline or aromatic product. In addition, after the naphtha fraction was distilled at once from the atmospheric distillation apparatus 1, all the naphtha fractions were hydrorefined in the presence of a catalyst in the hydrorefining apparatus 8 for naphtha, and then light naphtha and heavy naphtha. Sometimes separated into quality naphtha.

更に、灯油留分は、灯油精製装置9で精製されて灯油となり、軽油留分は、軽油用の水素化精製装置10において触媒存在下で水素化精製処理されて軽油となる。また、常圧蒸留装置1の底部に残った残油は、常圧蒸留装置1から取り出され、重油の調合材料とされたり、減圧蒸留装置で減圧蒸留されて軽質油の製造原料となる減圧留出油と減圧蒸留残油とに分離されたりする。このように、従来の原油の精製処理においては、分離された各留分のそれぞれに対して水素化精製(脱硫)などの精製処理が行われている。   Further, the kerosene fraction is refined by the kerosene refining device 9 to be kerosene, and the light oil fraction is hydrorefined in the presence of a catalyst in the hydrorefining device 10 for light oil to be light oil. The residual oil remaining at the bottom of the atmospheric distillation apparatus 1 is taken out from the atmospheric distillation apparatus 1 and used as a material for preparing heavy oil, or a vacuum distillation that is distilled under reduced pressure using a vacuum distillation apparatus and becomes a light oil production raw material. It is separated into the oil output and the vacuum distillation residue. As described above, in the conventional crude oil refining process, a refining process such as hydrorefining (desulfurization) is performed on each of the separated fractions.

しかしながら、上述のような各留分ごとに精製処理を行う方法では、設備構成が複雑になるため、設備コストが高くなる、エネルギー効率が悪化する、それぞれの装置について運転管理やメンテナンスが必要となる、という問題があった。このため、特に原油処理量が小さい場合に、装置構成がより簡素化された、コンパクトで低コストな処理方法が望まれていた。   However, in the method of performing the purification treatment for each fraction as described above, the equipment configuration is complicated, so that the equipment cost becomes high, energy efficiency deteriorates, and operation management and maintenance are required for each device. There was a problem. For this reason, there has been a demand for a compact and low-cost processing method with a simplified apparatus configuration, particularly when the amount of processed crude oil is small.

そのため、原油、或いは、原油からナフサ留分を除いた留分又は原油から残渣油を除いた留分などの留分に対して一括して水素化処理を行い、その後に常圧蒸留によりナフサ留分、灯油留分、軽油留分などの留分を分留する方法が提案されている。   Therefore, hydrogenation treatment is performed on crude oil, a fraction obtained by removing naphtha fraction from crude oil or a fraction obtained by removing residual oil from crude oil, and then subjected to hydrogenation treatment, followed by naphtha distillation by atmospheric distillation. A method of fractionating fractions such as a fraction, a kerosene fraction and a light oil fraction has been proposed.

具体的には、例えば特開平3−294390号公報(特許文献1)には、原油中のナフサ留分を蒸留分離した後、該ナフサ留分を除いた残りの留分を脱硫触媒と接触させて脱硫し、次いで蒸留して各製品に分離する原油の精製方法が記載されている。   Specifically, for example, in Japanese Patent Application Laid-Open No. 3-294390 (Patent Document 1), after a naphtha fraction in crude oil is distilled and separated, the remaining fraction excluding the naphtha fraction is brought into contact with a desulfurization catalyst. A method for refining crude oil is described which is desulfurized and then distilled to separate each product.

また、特開平7−82573号公報(特許文献2)には、原油を常圧蒸留して残油と留出油に分離した後、留出油を一括して同一の水素化処理装置で水素化処理する石油の処理方法が記載されている。   Japanese Patent Laid-Open No. 7-82573 (Patent Document 2) discloses that crude oil is distilled at atmospheric pressure and separated into a residual oil and a distillate, and then the distillate is collectively hydrogenated with the same hydrotreating apparatus. A method for treating petroleum to be treated is described.

更に、特開平7−300592号公報(特許文献3)には、原油を軽油及び軽油より低沸点の留分からなる留出油と残油とに分離した後、留出油を一括して水素化処理して得られた精製油を精留塔で所望の留分に分離し、精留塔で得られた軽油を水素化処理触媒と接触させ脱色処理する石油の処理方法が記載されている。   Furthermore, Japanese Patent Laid-Open No. 7-300592 (Patent Document 3) discloses that crude oil is separated into distillate and residual oil consisting of light oil and a fraction having a lower boiling point than light oil, and then distillate is hydrogenated in a lump. A method for treating petroleum is described in which a refined oil obtained by treatment is separated into desired fractions by a rectifying column, and a light oil obtained by the rectifying column is contacted with a hydrotreating catalyst to perform a decolorization treatment.

更にまた、特開2005−187823号公報(特許文献4)には、品質が良好でかつ安定した灯油・軽油を増産することができ、設備の簡素化が図れる方法として、原油又はナフサ留分を除いた原油を、特定の担体に周期律表第6、8、9又は10族に属する金属の少なくとも一種の金属を担持した触媒を用いて、一括して水素化処理する原油の水素化処理方法が記載されている。   Furthermore, Japanese Patent Application Laid-Open No. 2005-187823 (Patent Document 4) describes a method for increasing the production of kerosene / light oil with good quality and stability, and as a method for simplifying the equipment, crude oil or naphtha fraction. A method of hydrotreating crude oil, wherein the removed crude oil is collectively hydrotreated using a catalyst in which at least one kind of metal belonging to Group 6, 8, 9 or 10 of the periodic table is supported on a specific carrier. Is described.

一方、近年、灯油や軽油のさらなる低硫黄化が求められている。これに対して、例えば、脱硫率を向上させてより低硫黄分の軽油を得るためには、脱硫反応温度を上昇させるのが効果的である。しかしながら、脱硫反応温度を上昇させた場合には、好ましくない副反応を起こし易くなり、品質の安定した軽油留分を得ることが難しい。そのため、装置がコンパクトで、低コストで処理が可能で、更に、硫黄分が低く、品質の安定している灯油・軽油を得ることが可能な方法が望まれている。
特開平3−294390号公報 特開平7−82573号公報 特開平7−300592号公報 特開平7−305077号公報
On the other hand, in recent years, further reduction in sulfur of kerosene and light oil has been demanded. On the other hand, for example, in order to improve the desulfurization rate and obtain a light oil having a lower sulfur content, it is effective to raise the desulfurization reaction temperature. However, when the desulfurization reaction temperature is raised, an undesirable side reaction is likely to occur, and it is difficult to obtain a light oil fraction with stable quality. Therefore, there is a demand for a method capable of obtaining kerosene / light oil having a compact apparatus, capable of being processed at low cost, and having a low sulfur content and stable quality.
JP-A-3-294390 JP-A-7-82573 JP 7-300592 A Japanese Patent Laid-Open No. 7-305077

これに対し、本発明者らは、硫黄分が低く且つ品質が良好で安定した石油留分、特に軽油留分を、簡素化された精製設備を用いて、経済的に有利に製造できる炭化水素油の精製方法として、特定の蒸留性状を有し、かつ、特定の硫黄分分布を有する炭化水素油を一括して水素化精製処理し、該水素化精製処理された精製油を常圧蒸留装置にて常圧蒸留して、精製軽質ナフサ、精製重質ナフサ、精製灯油、精製軽油及び精製重質軽油に分離する炭化水素油の精製方法を新たに創作した。   On the other hand, the inventors of the present invention are hydrocarbons that can economically and advantageously produce a petroleum fraction with low sulfur content, good quality and stability, particularly a light oil fraction, using a simplified refining facility. As an oil refining method, hydrocarbon oils having specific distillation properties and having a specific sulfur content distribution are collectively hydrorefined and the hydrorefined refined oil is subjected to an atmospheric distillation apparatus. Has created a new method for refining hydrocarbon oils that are separated into refined light naphtha, refined heavy naphtha, refined kerosene, refined light oil and refined heavy gas oil.

しかしながら、上記精製方法を用いて炭化水素油から精製炭化水素油を製造するに当たっては、二環以上の芳香族炭化水素化合物の含有量が低くて脱硫剤を用いた脱硫が容易な灯油が望まれている(例えば特開2001−279273号公報参照)という観点から、灯油留分中の二環以上の芳香族炭化水素化合物の含有量を低減させることが好ましいという点において更に改善の余地があった。   However, when producing a refined hydrocarbon oil from a hydrocarbon oil using the above-described refining method, kerosene that has a low content of bicyclic or higher aromatic hydrocarbon compounds and can be easily desulfurized using a desulfurizing agent is desired. (For example, see JP-A-2001-279273), there is room for further improvement in that it is preferable to reduce the content of the aromatic hydrocarbon compound of two or more rings in the kerosene fraction. .

本発明者らは、上記目的を達成するために鋭意検討した結果、特定の性状を有する炭化水素油を原料として水素化処理することにより、二環以上の芳香族炭化水素化合物の含有量を低減した沸点範囲が150〜250℃の留分を含有する精製炭化水素油を得ることが可能であることを見出し、本発明を完成させるに至った。   As a result of intensive studies to achieve the above object, the present inventors reduced the content of bicyclic or higher aromatic hydrocarbon compounds by hydrotreating hydrocarbon oils having specific properties as raw materials. The inventors have found that it is possible to obtain a refined hydrocarbon oil containing a fraction having a boiling point range of 150 to 250 ° C., and have completed the present invention.

即ち、本発明の精製炭化水素油の製造方法は、10容量%留出温度が35〜80℃、97容量%留出温度が250〜420℃の蒸留性状を有し、沸点範囲が150℃以上250℃未満の留分の割合が20〜35容量%であり、且つ、沸点範囲が30℃以上150℃未満の留分に含まれる硫黄分をS1、沸点範囲が150℃以上250℃未満の留分に含まれる硫黄分をS2、沸点範囲が250℃以上350℃未満の留分に含まれる硫黄分をS3とした場合にS1>S2、S1>S3の関係を満たす炭化水素油を水素化精製処理することを特徴とする。このように、特定の性状を有する炭化水素油を原料として水素化精製処理することにより、沸点範囲が150〜250℃の留分に含まれる二環以上の芳香族炭化水素化合物の含有量を低減して精製炭化水素油を得ることが可能となる。また、硫黄分が低く品質が安定した性状を有する沸点範囲が250〜350℃の留分を含有する留分を得ることができる。ここで、本発明において、蒸留性状とはJIS K2254およびJIS K2601に従い評価したものを、硫黄分とはJIS K2541に従い評価したものを指す。また、沸点範囲が150℃以上250℃未満の留分の割合とは原料として用いる炭化水素油を常圧蒸留した場合に沸点範囲が150℃以上250℃未満の留分として留出するものが当該炭化水素油中で占める割合を指す。   That is, the method for producing a refined hydrocarbon oil of the present invention has a distillation property of 10% by volume distillation temperature of 35 to 80 ° C., 97% by volume distillation temperature of 250 to 420 ° C., and a boiling point range of 150 ° C. or more. The proportion of the fraction below 250 ° C. is 20 to 35% by volume, and the sulfur content contained in the fraction having a boiling point range of 30 ° C. or higher and lower than 150 ° C. is S1, and the boiling point range is 150 ° C. or higher and lower than 250 ° C. Hydrotreating hydrocarbon oils satisfying the relationship of S1> S2 and S1> S3, where S2 is the sulfur content contained in the water and S3 is the sulfur content contained in the fraction having a boiling range of 250 ° C. or higher and less than 350 ° C. It is characterized by processing. In this way, by hydrotreating using hydrocarbon oils having specific properties as raw materials, the content of aromatic hydrocarbon compounds having two or more rings contained in the fraction having a boiling range of 150 to 250 ° C. is reduced. Thus, it becomes possible to obtain a refined hydrocarbon oil. In addition, a fraction containing a fraction having a boiling point range of 250 to 350 ° C. having a low sulfur content and stable quality can be obtained. Here, in the present invention, the distillation properties refer to those evaluated according to JIS K2254 and JIS K2601, and the sulfur content refers to those evaluated according to JIS K2541. In addition, the ratio of the fraction having a boiling range of 150 ° C. or more and less than 250 ° C. means that the hydrocarbon oil used as a raw material is distilled as a fraction having a boiling range of 150 ° C. or more and less than 250 ° C. Refers to the proportion of hydrocarbon oil.

また、本発明の精製炭化水素油は、上記精製炭化水素油の製造方法を用いて製造した精製炭化水素油であって、当該精製炭化水素油中の沸点範囲が150〜250℃の留分の、硫黄分が1.0質量ppm以下であり、且つ、二環以上の芳香族炭化水素化合物の含有量が0.3容量%未満であることを特徴とする。ここで、本発明において、二環以上の芳香族炭化水素化合物の含有量とは、社団法人石油学会により発行されている石油学会誌JPI−5S−49−97「炭化水素タイプ試験法−高速液体クロマトグラフ法」に記載の方法に準拠して測定される各芳香族分含有量の容量百分率(容量%)から導出されるものである。   Moreover, the refined hydrocarbon oil of the present invention is a refined hydrocarbon oil produced by using the method for producing the refined hydrocarbon oil, and a fraction having a boiling point range of 150 to 250 ° C. in the refined hydrocarbon oil. The sulfur content is 1.0 mass ppm or less, and the content of the bicyclic or higher aromatic hydrocarbon compound is less than 0.3% by volume. Here, in the present invention, the content of the aromatic hydrocarbon compound having two or more rings is the Petroleum Society Journal JPI-5S-49-97 “Hydrocarbon Type Test Method—High-Speed Liquid” published by the Japan Petroleum Institute. It is derived from the volume percentage (volume%) of each aromatic content measured according to the method described in “Chromatograph Method”.

本発明によれば、特定の性状をもつ炭化水素油を原料として用い、該炭化水素油を一括水素化精製処理(脱硫)して精製炭化水素油を製造するので、コンパクトな装置で簡素化された精製方法により、硫黄分が低く品質が安定した留分、特に軽油留分を得ることができると共に、精製炭化水素油中の沸点範囲が150〜250℃の留分に含まれる二環以上の芳香族炭化水素化合物の含有量を低減した精製炭化水素油を得ることができる。   According to the present invention, a hydrocarbon oil having a specific property is used as a raw material, and the hydrocarbon oil is collectively hydrorefined (desulfurized) to produce a refined hydrocarbon oil. With a refined purification method, a fraction having a low sulfur content and a stable quality, particularly a light oil fraction, can be obtained, and at least two rings included in a fraction having a boiling point range of 150 to 250 ° C. in the refined hydrocarbon oil. A refined hydrocarbon oil in which the content of the aromatic hydrocarbon compound is reduced can be obtained.

図2に示す、本発明の精製炭化水素油の製造方法の一例を説明するための構成図を参照しながら、以下に、本発明を詳細に説明する。   Hereinafter, the present invention will be described in detail with reference to the block diagram for explaining an example of the method for producing a refined hydrocarbon oil of the present invention shown in FIG.

[炭化水素油]
本発明の精製炭化水素油の製造方法においては、原料となる炭化水素油として、10容量%留出温度が35〜80℃、好ましくは36〜72℃、97容量%留出温度が250〜420℃、好ましくは250〜400℃の蒸留性状を有し、当該炭化水素油中の、常圧蒸留して得られる沸点範囲が150℃以上250℃未満の留分の割合が20〜35容量%、好ましくは20〜30容量%であり、且つ、常圧蒸留して得られる沸点範囲が30℃以上150℃未満の留分に含まれる硫黄分(S1)が、沸点範囲が150℃以上250℃未満の留分に含まれる硫黄分(S2)および沸点範囲が250℃以上350℃未満の留分に含まれる硫黄分(S3)より多い炭化水素油を用いる。なお、炭化水素油としては、上記蒸留性状に加えて、95容量%留出温度が230〜350℃、好ましくは250〜340℃の蒸留性状も有する炭化水素油を用いても良い。
[Hydrocarbon oil]
In the method for producing the refined hydrocarbon oil of the present invention, the 10% by volume distillation temperature is 35 to 80 ° C., preferably 36 to 72 ° C., and the 97% by volume distillation temperature is 250 to 420 as the hydrocarbon oil used as a raw material. 20 to 35% by volume of a fraction having a distillation property of 150 ° C. or more and less than 250 ° C., having a distillation property of 250 to 400 ° C., and having a boiling point range obtained by atmospheric distillation in the hydrocarbon oil. Preferably, it is 20 to 30% by volume, and the sulfur content (S1) contained in the fraction having a boiling point range of 30 ° C. or higher and lower than 150 ° C. obtained by atmospheric distillation has a boiling point range of 150 ° C. or higher and lower than 250 ° C. Hydrocarbon oil having a sulfur content (S2) contained in this fraction and a sulfur content (S3) greater than the sulfur content (S3) contained in a fraction having a boiling point range of 250 ° C. or higher and lower than 350 ° C. is used. The hydrocarbon oil may be a hydrocarbon oil having a distillation property of 95% by volume distillation temperature of 230 to 350 ° C., preferably 250 to 340 ° C. in addition to the above distillation properties.

ここで、S1がS2及びS3より多いことは、蒸留装置で沸点30℃以上150℃未満、150℃以上250℃未満及び250℃以上350℃未満となるように原料となる炭化水素油の分留を行い、各留分に含まれる硫黄分について比較することにより判断できる。なお、蒸留装置とは、液体混合物を沸点の差を利用して分離する装置で、常温、常圧で液体の混合物の他、固体の混合物でも温度と圧力とを調節することで液体混合物として蒸留により分離できる装置をいう。   Here, the fact that S1 is larger than S2 and S3 means that the hydrocarbon oil used as a raw material has a boiling point of 30 to 150 ° C., 150 to 250 ° C. and 250 to 350 ° C. in a distillation apparatus. It can judge by comparing about the sulfur content contained in each fraction. A distillation device is a device that separates a liquid mixture by utilizing the difference in boiling point. In addition to a liquid mixture at room temperature and normal pressure, a solid mixture can be distilled as a liquid mixture by adjusting the temperature and pressure. Means a device that can be separated by

本発明においては、原料となる炭化水素油のS1はS2およびS3より多く、好ましくは、S1がS2の1.2〜5倍であり、また、S1がS3の1.2〜5倍である。なお、炭化水素油中のS1は200〜8000質量ppmの範囲が好ましく、S2およびS3は10〜2500質量ppmの範囲が好ましい。   In the present invention, S1 of the hydrocarbon oil used as a raw material is larger than S2 and S3. Preferably, S1 is 1.2 to 5 times S2, and S1 is 1.2 to 5 times S3. . In addition, S1 in hydrocarbon oil has the preferable range of 200-8000 mass ppm, and S2 and S3 have the preferable range of 10-2500 mass ppm.

本発明における水素化精製処理(脱硫)は、炭化水素油を分留することなく一括して水素化精製処理することから、各留分に含有される硫黄分の脱硫反応性の違いにより、より軽質留分の脱硫反応性が高くなる。そのため、S1>S2、S1>S3の関係を満たす炭化水素油を原料として用いた場合、沸点範囲が150℃以上250℃未満の留分や沸点範囲が250℃以上350℃未満の留分の脱硫率に着目して、反応温度を設定することができる。例えば、サルファーフリー軽油(硫黄分10質量ppm以下)の精製に適した反応条件を設定した場合には、軽油留分より軽質な留分はより硫黄分が少なくなり、軽質ナフサ、重質ナフサのように、品質上軽油より硫黄分を少なくする必要が有るものについても、必要とする品質を満足する製品が得られる。   Since the hydrorefining treatment (desulfurization) in the present invention is a hydrorefining treatment in a lump without fractionating hydrocarbon oil, due to the difference in desulfurization reactivity of sulfur contained in each fraction, Desulfurization reactivity of the light fraction is increased. Therefore, when hydrocarbon oil satisfying the relations of S1> S2 and S1> S3 is used as a raw material, desulfurization of a fraction having a boiling point range of 150 ° C. or more and less than 250 ° C. or a fraction having a boiling point range of 250 ° C. or more and less than 350 ° C. Focusing on the rate, the reaction temperature can be set. For example, when reaction conditions suitable for refining sulfur-free gas oil (sulfur content of 10 mass ppm or less) are set, the lighter fraction has a lower sulfur content than the light oil fraction, and light naphtha and heavy naphtha As described above, a product satisfying the required quality can be obtained even if it is necessary to reduce the sulfur content from light oil.

上記炭化水素油としては、具体的には、天然ガスコンデンセートを挙げることができる。天然ガスコンデンセートとは、天然ガス田より天然ガスの採取、精製を行う過程で得られる常温、常圧で液体の炭化水素のことであり、油田から得られる一般の原油に比べて極めて軽質でナフサに近い性状である。天然ガスコンデンセートは、石油類の比重として欧米諸国で広く使われているAPI比重で50以上の軽質油で、かつ硫黄分が少ないことから、API比重20〜50で硫黄分0〜3%程度である原油よりもガソリンなどの軽質の石油製品を多く精製できる原料油である。天然ガスコンデンセートとしては、例えば、中東産のサウスパースコンデンセート、ノースフィールドコンデンセートを例示することができるが、これらに限定されるものではない。また、本発明の炭化水素油としては、異なる性状を有する複数の炭化水素油を混合して、上記蒸留性状および硫黄分を有する炭化水素油としたものを用いることもできる。   Specific examples of the hydrocarbon oil include natural gas condensate. Natural gas condensate is a liquid hydrocarbon at normal temperature and pressure obtained during the process of collecting and refining natural gas from a natural gas field, and is extremely light and naphtha compared to general crude oil obtained from oil fields. It is close to the property. Natural gas condensate is a light oil with an API specific gravity of 50 or more, which is widely used in Western countries as a specific gravity of petroleum, and has a low sulfur content, so it has an API specific gravity of 20 to 50 and a sulfur content of about 0 to 3%. It is a feedstock that can refine more light petroleum products such as gasoline than some crude oil. Examples of natural gas condensate include, but are not limited to, South Perth condensate and Northfield condensate produced in the Middle East. In addition, as the hydrocarbon oil of the present invention, a hydrocarbon oil having a distillation property and a sulfur content obtained by mixing a plurality of hydrocarbon oils having different properties can be used.

[水素化精製処理]
本発明の精製炭化水素油の製造方法では、原料となる上記炭化水素油を一括して水素化精製装置12に送り、触媒の存在下、炭化水素油と水素(H2)とを接触させて、脱硫などの水素化精製処理を行う。ここで、上記水素化精製装置12としては、気液下向並流型反応器を用いることが好ましい。
[Hydro-refining treatment]
In the method for producing a refined hydrocarbon oil according to the present invention, the hydrocarbon oil as a raw material is collectively sent to the hydrotreating apparatus 12, and the hydrocarbon oil and hydrogen (H 2 ) are brought into contact with each other in the presence of a catalyst. Hydrotreating treatment such as desulfurization is performed. Here, as the hydrorefining apparatus 12, it is preferable to use a gas-liquid downward co-current reactor.

また、水素化精製処理の条件としては、圧力が2〜8MPa、特には5〜8MPaの範囲であることが好ましく、反応温度が280〜380℃、特には310〜360℃の範囲であることが好ましく、H2/油比が50〜200Nm3/kL、特には100〜200Nm3/kLの範囲であることが好ましく、液空間速度(LHSV)が0.1〜5h-1、特には1〜3h-1の範囲であることが好ましい。なお、特に図示しないが、必要に応じて、水素化精製処理された精製炭化水素油の一部を再度水素化精製装置12に返送して水素化精製処理しても良い。 Further, as conditions for the hydrorefining treatment, the pressure is preferably 2 to 8 MPa, particularly 5 to 8 MPa, and the reaction temperature is 280 to 380 ° C., particularly 310 to 360 ° C. Preferably, the H 2 / oil ratio is in the range of 50 to 200 Nm 3 / kL, particularly 100 to 200 Nm 3 / kL, and the liquid space velocity (LHSV) is 0.1 to 5 h −1 , particularly 1 to 1. A range of 3h -1 is preferred. Although not particularly illustrated, a part of the refined hydrocarbon oil that has been hydrorefined may be returned to the hydrorefining apparatus 12 and hydrorefined as necessary.

ここで、水素化精製処理に用いる水素源としては、水素含有ガスである限り特に制限されるものではないが、純度75%以上のものが好ましく、80%以上のものが更に好ましい。該水素源として、具体的には、後述する精製重質ナフサの接触改質処理を行う接触改質装置14から副生する水素等を使用することができる。   Here, the hydrogen source used for the hydrorefining treatment is not particularly limited as long as it is a hydrogen-containing gas, but preferably has a purity of 75% or more, more preferably 80% or more. Specifically, hydrogen generated as a by-product from the catalytic reforming apparatus 14 that performs catalytic reforming treatment of purified heavy naphtha, which will be described later, can be used as the hydrogen source.

[触媒]
水素化精製処理用の触媒としては、100〜300m/gの表面積を有するアルミナ、シリカアルミナ、シリカ又はゼオライト等の担体に、活性金属としてコバルト、ニッケル、モリブデン、タングステンから選ばれる2種以上の元素を担持した触媒を使用することができる。上記元素の代表的な組み合わせとしては、コバルト及びモリブデン(Co−Mo)、ニッケル及びモリブデン(Ni−Mo)、ニッケル及びタングステン(Ni−W)、ニッケル、コバルト及びモリブデン(Ni−Co−Mo)が挙げられる。活性金属の担持量としては、モリブデンは5〜20質量%、コバルト及びニッケルは0.5〜5質量%、タングステンは10〜30質量%が好ましい。
[catalyst]
As a catalyst for hydrorefining treatment, two or more kinds selected from cobalt, nickel, molybdenum and tungsten as active metals on a support such as alumina, silica alumina, silica or zeolite having a surface area of 100 to 300 m 2 / g. An element-supported catalyst can be used. Typical combinations of the above elements include cobalt and molybdenum (Co—Mo), nickel and molybdenum (Ni—Mo), nickel and tungsten (Ni—W), nickel, cobalt and molybdenum (Ni—Co—Mo). Can be mentioned. The supported amount of the active metal is preferably 5 to 20% by mass for molybdenum, 0.5 to 5% by mass for cobalt and nickel, and 10 to 30% by mass for tungsten.

[常圧蒸留装置での常圧蒸留]
本発明の精製炭化水素油の製造方法では、水素化精製装置12で水素化精製処理した炭化水素油を常圧蒸留装置15に送り、常圧蒸留して、精製LPガス、精製軽質ナフサ、精製重質ナフサ、精製灯油、精製軽油及び精製重質軽油などの各留分に分離しても良い。ここで、精製ナフサとは、10容量%留出温度が50℃以上で90容量%留出温度が150℃以下の留分であり、沸点範囲が30〜150℃の留分を含有する留分をいう。この内の精製軽質ナフサとは、沸点が30〜100℃程度の留分を、精製重質ナフサとは沸点が75〜200℃程度の留分をいう。また、精製灯油とは、引火点が40℃以上で95容量%留出温度が300℃以下の留分を、精製軽油とは、引火点が45℃以上で90容量%留出温度が360℃以下、流動点が5℃以下の留分をいう。なお、引火点とはJIS K2265に準拠して測定した値を、流動点とはJIS K2269に準拠して測定した値を指す。
[Atmospheric distillation with atmospheric distillation equipment]
In the method for producing a refined hydrocarbon oil of the present invention, the hydrocarbon oil hydrotreated by the hydrotreating device 12 is sent to the atmospheric distillation device 15 and subjected to atmospheric distillation to produce purified LP gas, refined light naphtha, refined You may isolate | separate into each fraction, such as heavy naphtha, refined kerosene, refined light oil, and refined heavy light oil. Here, the purified naphtha is a fraction having a 10% by volume distillation temperature of 50 ° C. or more and a 90% by volume distillation temperature of 150 ° C. or less, and containing a fraction having a boiling point range of 30 to 150 ° C. Say. Among these, the refined light naphtha means a fraction having a boiling point of about 30 to 100 ° C., and the refined heavy naphtha means a fraction having a boiling point of about 75 to 200 ° C. Refined kerosene is a fraction having a flash point of 40 ° C. or higher and a 95% by volume distillation temperature of 300 ° C. or less, and refined light oil is a flash point of 45 ° C. or higher and a 90% by volume distillation temperature of 360 ° C. Hereinafter, it refers to a fraction having a pour point of 5 ° C. or lower. The flash point refers to a value measured according to JIS K2265, and the pour point refers to a value measured according to JIS K2269.

なお、水素化精製処理した炭化水素油を常圧蒸留するに当たっては、常圧蒸留装置15で精製ナフサ留分を一括で留出させた後に、全精製ナフサ留分をナフサ分離装置16に送り、精製軽質ナフサ及び精製重質ナフサに分離してもよい。   In order to atmospherically distill the hydrorefined hydrocarbon oil, after the purified naphtha fraction is distilled at once by the atmospheric distillation apparatus 15, the whole refined naphtha fraction is sent to the naphtha separation apparatus 16, You may isolate | separate into refined light naphtha and refined heavy naphtha.

また、特に図示しないが、必要に応じて、分離した精製軽油及び精製重質軽油を再度水素化精製装置12に返送して水素化精製処理してもよい。   Although not particularly shown, the refined light oil and the refined heavy gas oil that have been separated may be returned to the hydrorefining device 12 and hydrorefined as necessary.

上述したような水素化精製処理並びに分留によって、図2に示すように、炭化水素油から、軽質ガス、LPガス、精製ナフサ(精製軽質ナフサ、精製重質ナフサ)、精製灯油、精製軽油、精製重質軽油の各留分が得られる。   By hydrotreating and fractionation as described above, as shown in FIG. 2, from hydrocarbon oil, light gas, LP gas, refined naphtha (refined light naphtha, refined heavy naphtha), refined kerosene, refined light oil, Each fraction of refined heavy gas oil is obtained.

ここで、軽質ガスは、アミン精製装置17で酸性ガスを分離し、燃料ガスとする一方、分離した酸性ガスを硫黄回収装置18に送り硫黄を回収してもよい。   Here, the light gas may be separated into acidic gas by the amine purifying device 17 and used as fuel gas, while the separated acidic gas may be sent to the sulfur recovery device 18 to recover sulfur.

精製軽質ナフサは、そのままガソリンに調合することができる他、エチレン分解装置原料(石化原料)としても良く、必要に応じて改質処理やスイートニング処理を行っても良い。精製重質ナフサは、接触改質装置14に送られ、接触改質装置14で異性化や芳香族化した後、ガソリンに調合したり、芳香族製品としたりすることができる。この接触改質装置14で副生する水素は、上述のように水素化精製装置12に送って水素化精製処理用の水素源として利用することができ、また副生するLPガス分は、LPガス処理装置19から得られる精製LPガスに混合することができる。   The refined light naphtha can be directly blended with gasoline, or it can be used as an ethylene cracker raw material (a petrochemical raw material), and a reforming process or a sweetening process may be performed as necessary. The refined heavy naphtha is sent to the catalytic reforming device 14 and isomerized or aromatized by the catalytic reforming device 14, and then blended into gasoline or made into an aromatic product. The hydrogen produced as a by-product in the catalytic reforming device 14 can be sent to the hydrotreating device 12 as described above and used as a hydrogen source for hydrotreating treatment. It can be mixed with purified LP gas obtained from the gas processing device 19.

更に、上述のようにして得られた精製炭化水素油を常圧蒸留して得た精製灯油は、硫黄分が1.0質量ppm以下であり、且つ、二環以上の芳香族炭化水素化合物、例えば、ナフタレン、ビフェニル等の二環芳香族炭化水素化合物、アントラセン等の三環芳香族炭化水素化合物、クリセン、ピレン、コロネン等の多環芳香族炭化水素化合物などの含有量が0.3容量%未満であることが好ましい。そして、この精製灯油は、そのまま製品灯油とすることができる。ここで、二環以上の芳香族炭化水素化合物の含有量とは、社団法人石油学会により発行されている石油学会誌JPI−5S−49−97「炭化水素タイプ試験法−高速液体クロマトグラフ法」に記載の方法に準拠して測定される各芳香族分(芳香族炭化水素化合物)含有量の容量百分率(容量%)から導出されるものである。   Furthermore, the refined kerosene obtained by atmospheric distillation of the refined hydrocarbon oil obtained as described above has a sulfur content of 1.0 mass ppm or less, and an aromatic hydrocarbon compound having two or more rings, For example, the content of bicyclic aromatic hydrocarbon compounds such as naphthalene and biphenyl, tricyclic aromatic hydrocarbon compounds such as anthracene, and polycyclic aromatic hydrocarbon compounds such as chrysene, pyrene, and coronene is 0.3% by volume. It is preferable that it is less than. And this refined kerosene can be used as a product kerosene as it is. Here, the content of the aromatic hydrocarbon compound having two or more rings is the Petroleum Institute Journal JPI-5S-49-97 “Hydrocarbon Type Test Method—High Performance Liquid Chromatograph Method” published by the Japan Petroleum Institute. Is derived from the volume percentage (volume%) of each aromatic content (aromatic hydrocarbon compound) content measured in accordance with the method described in 1. above.

また、精製軽油も、そのまま製品軽油とすることができる。なお、常圧蒸留装置15により分離された精製軽油は、硫黄分10質量ppm以下の軽油(サルファーフリー軽油)であることが好ましい。また、精製重質軽油は、接触分解装置(図示せず)に送り、そこで接触分解によりガソリンに転換することができる。   Refined light oil can also be used as product light oil as it is. In addition, it is preferable that the refined light oil isolate | separated by the atmospheric distillation apparatus 15 is a light oil (sulfur free light oil) with a sulfur content of 10 mass ppm or less. The refined heavy gas oil can be sent to a catalytic cracking device (not shown) where it can be converted to gasoline by catalytic cracking.

上述した本発明の精製炭化水素油の製造方法は、原料となる炭化水素油を一括して同一の水素化精製装置12で水素化精製処理することにより、原油を蒸留により細かく分留し、その後各留分毎に水素化精製処理する場合と比べ、製油所の装置構成が簡略化され、建設コストや、設置スペースを削減できる。また、原油処理量が少ない場合であっても装置構成のコンパクト化が可能となる。更に、特定の性状を有する炭化水素油を原料として用いているので、二環以上の芳香族炭化水素化合物の含有量を低減した沸点範囲が150〜250℃の留分を含有する精製炭化水素油を得ることができる。   In the method for producing the refined hydrocarbon oil of the present invention described above, the crude oil is finely fractionated by distillation by hydrotreating the hydrocarbon oil as a raw material in the same hydrorefining device 12, and thereafter Compared with the case of hydrotreating each fraction, the refinery equipment configuration is simplified, and the construction cost and installation space can be reduced. Further, the apparatus configuration can be made compact even when the crude oil processing amount is small. Furthermore, since a hydrocarbon oil having a specific property is used as a raw material, a refined hydrocarbon oil containing a fraction having a boiling point range of 150 to 250 ° C. in which the content of an aromatic hydrocarbon compound having two or more rings is reduced. Can be obtained.

[重金属の吸着除去]
なお、上記炭化水素油、特に天然ガスコンデンセートは、一般的な原油に比べて水銀等の重金属分を多く含有することがある。そのため、必要に応じて吸着剤による重金属の吸着除去装置を設置して、水素化精製処理した精製炭化水素油の分留後の留分である精製軽質ナフサ、精製重質ナフサ、場合によっては精製灯油留分について、重金属、特には水銀の吸着除去を行い、各精製留分の品質を更に高めることができる。なお、吸着除去装置(図示せず)は、常圧蒸留装置15の直後に設置することが好ましい。また、重金属の吸着除去には、活性炭などの吸着剤を使用することができる。
[Adsorption removal of heavy metals]
The hydrocarbon oil, particularly natural gas condensate, may contain a larger amount of heavy metals such as mercury than general crude oil. Therefore, if necessary, a heavy metal adsorption / removal device using an adsorbent is installed, and a refined light naphtha, a refined heavy naphtha, or a refined product after the fractionation of the hydrorefined refined hydrocarbon oil is purified. With respect to the kerosene fraction, heavy metals, particularly mercury can be removed by adsorption, and the quality of each refined fraction can be further enhanced. In addition, it is preferable to install an adsorption removal apparatus (not shown) immediately after the atmospheric distillation apparatus 15. Further, an adsorbent such as activated carbon can be used to remove heavy metals by adsorption.

以下に、実施例を挙げて本発明を更に詳しく説明するが、本発明は下記の実施例に何ら限定されるものではない。   Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to the following examples.

なお、実施例及び比較例において、蒸留性状、密度、硫黄分、芳香族分含有量は、以下の方法に従って評価した。
・蒸留性状:JIS K2254およびJIS K2601
・密度:JIS K2249
・硫黄分:JIS K2541
・芳香族分含有量:[沸点150℃未満の留分]JIS K2536
[沸点150℃以上の留分]JPI−5S−49−97
In Examples and Comparative Examples, distillation properties, density, sulfur content, and aromatic content were evaluated according to the following methods.
Distillation properties: JIS K2254 and JIS K2601
・ Density: JIS K2249
・ Sulfur content: JIS K2541
Aromatic content: [Fraction with boiling point less than 150 ° C.] JIS K2536
[Fraction having a boiling point of 150 ° C. or higher] JPI-5S-49-97

(原料炭化水素油の性状)
一般的な天然ガスコンデンセートとして、イランのサウスパースガス田から得られたコンデンセート(サウスパースコンデンセート)の性状を表1に、該コンデンセートの各留分の収率および性状を表2に示す。なお、他の例も含めて、収率の合計が100%にならないのは、蒸留ロスのためである。
(Properties of raw hydrocarbon oil)
As general natural gas condensate, properties of condensate (South Perth Condensate) obtained from the South Perth gas field in Iran are shown in Table 1, and yield and properties of each fraction of the condensate are shown in Table 2. In addition, including other examples, the total yield does not reach 100% because of distillation loss.

Figure 2010111771
Figure 2010111771

Figure 2010111771
Figure 2010111771

(実施例1)
上記のサウスパースコンデンセートを原料炭化水素油として用いた。内径10mm×長さ300mmの反応器にCo−Mo系触媒(アルミナ担体にコバルトを2.4質量%、モリブデンを15.3質量%担持した、表面積が199m/gである触媒)を10cc充填してなる下向並流式の反応器を用い、水素純度:100%、圧力:5MPa、反応温度:290〜350℃、H2/油比:200Nm3/kL、LHSV:2.0h-1の反応条件で、原料炭化水素油を一括して水素化精製処理した。
Example 1
The above South Perth Condensate was used as a raw material hydrocarbon oil. 10 cc of Co-Mo catalyst (catalyst having a surface area of 199 m 2 / g supported by 2.4 mass% cobalt and 15.3 mass% molybdenum on an alumina support) is packed in a reactor having an inner diameter of 10 mm and a length of 300 mm. The hydrogen purity is 100%, the pressure is 5 MPa, the reaction temperature is 290 to 350 ° C., the H 2 / oil ratio is 200 Nm 3 / kL, and the LHSV is 2.0 h −1. Under these reaction conditions, the raw material hydrocarbon oils were collectively hydrorefined.

水素化精製処理後の精製炭化水素油について、ガス分(H、炭素数4以下の炭化水素)を分離し、更に分留器に移して常圧蒸留して、沸点範囲が150℃未満の留分、沸点範囲が150〜250℃の留分、沸点範囲が250℃超350℃未満の留分、及び沸点350℃以上の留分の各留分に分離し、これら各留分のうち沸点範囲が150〜250℃の留分の残留硫黄濃度及び芳香族分含有量を評価した。結果を表4に示す。 For the refined hydrocarbon oil after hydrorefining treatment, the gas component (H 2 , hydrocarbon having 4 or less carbon atoms) is separated, and further transferred to a fractionator and subjected to atmospheric distillation, and the boiling point range is less than 150 ° C. The fraction is separated into a fraction having a boiling range of 150 to 250 ° C, a fraction having a boiling range of more than 250 ° C and less than 350 ° C, and a fraction having a boiling point of 350 ° C or higher. Residual sulfur concentration and aromatic content of fractions with a range of 150-250 ° C. were evaluated. The results are shown in Table 4.

(実施例2)
水素化精製処理に使用した触媒を、市販のNi−Mo系触媒(アルミナ担体にニッケルを2.4質量%、モリブデンを14.7質量%担持した、表面積が232m/gである触媒)にした以外は実施例1と同様にして水素化精製処理および分留を行い、各留分のうち沸点範囲が150〜250℃の留分の残留硫黄濃度及び芳香族分含有量を評価した。結果を表4に示す。
(Example 2)
The catalyst used in the hydrotreating process, a commercially available Ni-Mo-based catalyst (2.4 wt% nickel on an alumina carrier, molybdenum was supported 14.7 wt%, surface area catalyst is 232m 2 / g) to The hydrorefining treatment and fractional distillation were carried out in the same manner as in Example 1 except that the residual sulfur concentration and aromatic content of fractions having a boiling point range of 150 to 250 ° C. were evaluated. The results are shown in Table 4.

(実施例3)
水素化精製処理に使用した触媒を、市販のNi−Co−Mo系触媒(アルミナ担体にニッケルを0.6質量%、コバルトを2.8質量%、モリブデンを14.7質量%担持した、表面積が205m/gである触媒)にした以外は実施例1と同様にして水素化精製処理および分留を行い、各留分のうち沸点範囲が150〜250℃の留分の残留硫黄濃度及び芳香族分含有量を評価した。結果を表4に示す。
(Example 3)
The catalyst used for the hydrorefining treatment was a commercially available Ni-Co-Mo catalyst (alumina support carrying 0.6 mass% nickel, 2.8 mass% cobalt, 14.7 mass% molybdenum, surface area There performed in a hydrogen-refining treatment and fractionation repeated except that the catalyst) is 205m 2 / g from example 1, the residual sulfur concentration and fraction having a boiling point range of the fraction 150 to 250 ° C. The aromatic content was evaluated. The results are shown in Table 4.

(比較例1)
原料炭化水素油として、サウスパースコンデンセートの沸点範囲が150℃以上250℃未満の留分を用いた。内径25mm×長さ1080mmの反応器に市販のCo−Mo系触媒(アルミナ担体にコバルトを2.4質量%、モリブデンを15.3質量%担持した、表面積が199m/gである触媒)を50cc充填してなる下向並流式の反応器を用い、水素純度:100%、圧力:5MPa、反応温度:290〜350℃、H2/油比:200Nm3/kL、LHSV:2.0h-1の反応条件で、原料炭化水素油を水素化精製処理した。得られた精製炭化水素油中の沸点範囲が150〜250℃の留分の芳香族分含有量及び残留硫黄濃度を評価した。使用したサウスパースコンデンセートの沸点範囲が150℃以上250℃未満の留分の性状を表3に、結果を表4に示す。
(Comparative Example 1)
As the raw material hydrocarbon oil, a fraction having a boiling point range of 150 ° C. or higher and lower than 250 ° C. of South Perth condensate was used. A commercially available Co-Mo-based catalyst (a catalyst having a surface area of 199 m 2 / g in which 2.4 mass% cobalt and 15.3 mass% molybdenum are supported on an alumina carrier) in a reactor having an inner diameter of 25 mm and a length of 1080 mm. Using a downward co-current type reactor filled with 50 cc, hydrogen purity: 100%, pressure: 5 MPa, reaction temperature: 290 to 350 ° C., H 2 / oil ratio: 200 Nm 3 / kL, LHSV: 2.0 h The raw hydrocarbon oil was hydrorefined under the reaction conditions of -1 . The aromatic content and the residual sulfur concentration of the fraction having a boiling point range of 150 to 250 ° C. in the obtained refined hydrocarbon oil were evaluated. Table 3 shows the properties of fractions having a boiling range of 150 ° C. or more and less than 250 ° C., and Table 4 shows the results.

Figure 2010111771
Figure 2010111771

Figure 2010111771
Figure 2010111771

従来の精製炭化水素油の製造方法の一例を説明するための構成図である。It is a block diagram for demonstrating an example of the manufacturing method of the conventional refinement | purification hydrocarbon oil. 本発明の精製炭化水素油の製造方法の一例を説明するための構成図である。It is a block diagram for demonstrating an example of the manufacturing method of the refine | purified hydrocarbon oil of this invention.

符号の説明Explanation of symbols

1,15 常圧蒸留装置
2,17 アミン精製装置
3,18 硫黄回収装置
4,19 LPガス処理装置
5 軽質ナフサ処理装置
6,8,10,12 水素化精製装置
7,14 接触改質装置
9 灯油精製装置
16 ナフサ分離装置
1,15 Atmospheric distillation equipment 2,17 Amine purification equipment 3,18 Sulfur recovery equipment 4,19 LP gas treatment equipment 5 Light naphtha treatment equipment 6,8,10,12 Hydrotreating equipment 7,14 Catalytic reforming equipment 9 Kerosene refiner 16 Naphtha separator

Claims (2)

10容量%留出温度が35〜80℃、97容量%留出温度が250〜420℃の蒸留性状を有し、
沸点範囲が150℃以上250℃未満の留分の割合が20〜35容量%であり、且つ、
沸点範囲が30℃以上150℃未満の留分に含まれる硫黄分をS1、沸点範囲が150℃以上250℃未満の留分に含まれる硫黄分をS2、沸点範囲が250℃以上350℃未満の留分に含まれる硫黄分をS3とした場合にS1>S2、S1>S3の関係を満たす
炭化水素油を水素化精製処理することを特徴とする精製炭化水素油の製造方法。
10% by volume distillation temperature of 35-80 ° C., 97% by volume distillation temperature of 250-420 ° C.
The fraction having a boiling range of 150 ° C. or higher and lower than 250 ° C. is 20 to 35% by volume, and
The sulfur content contained in the fraction having a boiling point range of 30 ° C. or more and less than 150 ° C. is S1, the sulfur content contained in the fraction having a boiling point range of 150 ° C. or more and less than 250 ° C. is S2, and the boiling point range is 250 ° C. or more and less than 350 ° C. A method for producing a refined hydrocarbon oil, comprising hydrotreating a hydrocarbon oil satisfying the relationships of S1> S2 and S1> S3 when the sulfur content in the fraction is S3.
請求項1に記載の製造方法を用いて製造した精製炭化水素油であって、当該精製炭化水素油中の沸点範囲が150〜250℃の留分の、硫黄分が1.0質量ppm以下であり、且つ、二環以上の芳香族炭化水素化合物の含有量が0.3容量%未満であることを特徴とする精製炭化水素油。   A refined hydrocarbon oil produced using the production method according to claim 1, wherein a fraction having a boiling point range of 150 to 250 ° C. in the refined hydrocarbon oil has a sulfur content of 1.0 mass ppm or less. A refined hydrocarbon oil characterized in that the content of an aromatic hydrocarbon compound having two or more rings is less than 0.3% by volume.
JP2008285642A 2008-11-06 2008-11-06 Method for producing purified hydrocarbon oil, and purified hydrocarbon oil Pending JP2010111771A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2008285642A JP2010111771A (en) 2008-11-06 2008-11-06 Method for producing purified hydrocarbon oil, and purified hydrocarbon oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2008285642A JP2010111771A (en) 2008-11-06 2008-11-06 Method for producing purified hydrocarbon oil, and purified hydrocarbon oil

Publications (1)

Publication Number Publication Date
JP2010111771A true JP2010111771A (en) 2010-05-20

Family

ID=42300579

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008285642A Pending JP2010111771A (en) 2008-11-06 2008-11-06 Method for producing purified hydrocarbon oil, and purified hydrocarbon oil

Country Status (1)

Country Link
JP (1) JP2010111771A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010111778A (en) * 2008-11-06 2010-05-20 Japan Energy Corp Method for producing purified hydrocarbon oil

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57170987A (en) * 1981-04-14 1982-10-21 Showa Denko Kk Removal of arsenic (as) in petroleum fraction
JPH01231920A (en) * 1988-03-10 1989-09-18 Inst Fr Petrole Removal of silver in hydrocarbon
JPH022873A (en) * 1987-11-14 1990-01-08 Jgc Corp Method for removing mercury
JPH05171160A (en) * 1991-12-18 1993-07-09 Jgc Corp Removal of mercury in liquid hydrocarbon
JPH10251667A (en) * 1997-01-13 1998-09-22 Taiyo Eng Kk Process for adsorptively removing trace metal from hydrocarbon fraction
JP2000063850A (en) * 1998-08-24 2000-02-29 Taiyo Engineering Kk Adsorbent for mercury in liquid hydrocarbon and method for adsorptive removal of mercury by using same
JP2006348186A (en) * 2005-06-16 2006-12-28 Nippon Oil Corp Kerosene
JP2007222751A (en) * 2006-02-22 2007-09-06 Idemitsu Kosan Co Ltd Hydrodesulfurization catalyst and hydrodesulfurization method for kerosene fraction
JP2007238832A (en) * 2006-03-10 2007-09-20 Mitsubishi Heavy Ind Ltd Method for treating natural gas condensate and system for treating the same

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57170987A (en) * 1981-04-14 1982-10-21 Showa Denko Kk Removal of arsenic (as) in petroleum fraction
JPH022873A (en) * 1987-11-14 1990-01-08 Jgc Corp Method for removing mercury
JPH01231920A (en) * 1988-03-10 1989-09-18 Inst Fr Petrole Removal of silver in hydrocarbon
JPH05171160A (en) * 1991-12-18 1993-07-09 Jgc Corp Removal of mercury in liquid hydrocarbon
JPH10251667A (en) * 1997-01-13 1998-09-22 Taiyo Eng Kk Process for adsorptively removing trace metal from hydrocarbon fraction
JP2000063850A (en) * 1998-08-24 2000-02-29 Taiyo Engineering Kk Adsorbent for mercury in liquid hydrocarbon and method for adsorptive removal of mercury by using same
JP2006348186A (en) * 2005-06-16 2006-12-28 Nippon Oil Corp Kerosene
JP2007222751A (en) * 2006-02-22 2007-09-06 Idemitsu Kosan Co Ltd Hydrodesulfurization catalyst and hydrodesulfurization method for kerosene fraction
JP2007238832A (en) * 2006-03-10 2007-09-20 Mitsubishi Heavy Ind Ltd Method for treating natural gas condensate and system for treating the same

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
JPN6012054364; 港谷昌成 他3名: '天然ガスコンデンセートの一括脱硫プロセス(1)' 石油・石油化学討論会講演要旨 38th, 20081105, p.88-89, 社団法人 石油学会 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010111778A (en) * 2008-11-06 2010-05-20 Japan Energy Corp Method for producing purified hydrocarbon oil

Similar Documents

Publication Publication Date Title
KR102339046B1 (en) Process and installation for the conversion of crude oil to petrochemicals having an improved ethylene yield
RU2666735C2 (en) Process for reining crude oil
JP5219247B2 (en) Method for producing low sulfur cracking gasoline base and unleaded gasoline composition
RU2615160C2 (en) Method of producing olefins and aromatic hydrocarbons
JPH0782573A (en) Method and apparatus for treating petroleum
JP2008297437A (en) Manufacturing method of ultralow-sulfur gas oil and manufacturing apparatus therefor
JP5345298B2 (en) Method for refining hydrocarbon oil
JPWO2007129736A1 (en) Method for producing dicyclopentadiene
JP5191865B2 (en) Manufacturing method of atmospheric distillation fraction
RU2592286C2 (en) Method for production of olefins and gasoline with low benzene content
JP2011231322A (en) Improved process for selective reduction of the contents of benzene and light unsaturated compound of various hydrocarbon fractions
JP5314546B2 (en) Method for pyrolysis of heavy oil
WO2009014303A1 (en) Method for producing feedstocks of high quality lube base oil from coking gas oil
JP5483861B2 (en) Production method of purified fraction
JP2010111771A (en) Method for producing purified hydrocarbon oil, and purified hydrocarbon oil
JP2011190306A (en) Method for producing kerosine-gas oil base material and alkylbenzenes
JP2010111770A (en) Method for producing purified hydrocarbon oil, and purified hydrocarbon oil
CA2853924A1 (en) Pretreatment of fcc naphthas and selective hydrotreating
JP2007119648A (en) Method for treating plastic cracked oil
WO2021055540A1 (en) Methods for producing needle coke from aromatic recovery complex bottoms
JP2004323485A (en) Method for producing high-purity cyclopentane
JP5207923B2 (en) Process for producing refined hydrocarbon oil
JP5371327B2 (en) Method for producing hydrocarbon oil
JP2020513401A (en) Method for producing hexadecahydropyrene
JP6346837B2 (en) Method for desulfurizing hydrocarbon oil, method for producing desulfurized oil, and method for suppressing decrease in catalyst activity

Legal Events

Date Code Title Description
A711 Notification of change in applicant

Free format text: JAPANESE INTERMEDIATE CODE: A712

Effective date: 20100831

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20110209

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20121005

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20121023

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20121221

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20130122

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20130319

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20131112