JP2000282060A - Gas turbine fuel oil, its production and power generation method - Google Patents
Gas turbine fuel oil, its production and power generation methodInfo
- Publication number
- JP2000282060A JP2000282060A JP11095203A JP9520399A JP2000282060A JP 2000282060 A JP2000282060 A JP 2000282060A JP 11095203 A JP11095203 A JP 11095203A JP 9520399 A JP9520399 A JP 9520399A JP 2000282060 A JP2000282060 A JP 2000282060A
- Authority
- JP
- Japan
- Prior art keywords
- oil
- gas turbine
- less
- light
- ppm
- 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.)
- Withdrawn
Links
- 239000000295 fuel oil Substances 0.000 title claims abstract description 128
- 238000000034 method Methods 0.000 title claims description 36
- 238000004519 manufacturing process Methods 0.000 title claims description 15
- 238000010248 power generation Methods 0.000 title description 21
- 239000003921 oil Substances 0.000 claims abstract description 215
- 239000007789 gas Substances 0.000 claims abstract description 121
- 238000004821 distillation Methods 0.000 claims abstract description 44
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 40
- 239000010779 crude oil Substances 0.000 claims abstract description 39
- 239000001257 hydrogen Substances 0.000 claims abstract description 23
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 23
- 239000003054 catalyst Substances 0.000 claims abstract description 21
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 21
- 229910052717 sulfur Inorganic materials 0.000 claims description 58
- 239000011593 sulfur Substances 0.000 claims description 58
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 53
- 238000000926 separation method Methods 0.000 claims description 44
- 238000005292 vacuum distillation Methods 0.000 claims description 19
- 238000002156 mixing Methods 0.000 claims description 16
- 238000011084 recovery Methods 0.000 claims description 15
- 239000002904 solvent Substances 0.000 claims description 14
- 229910052783 alkali metal Inorganic materials 0.000 claims description 11
- 150000001340 alkali metals Chemical class 0.000 claims description 11
- 239000012535 impurity Substances 0.000 claims description 11
- 238000005979 thermal decomposition reaction Methods 0.000 claims description 8
- 239000000446 fuel Substances 0.000 claims description 5
- 238000001256 steam distillation Methods 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- 230000005611 electricity Effects 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 238000009835 boiling Methods 0.000 description 23
- 238000006243 chemical reaction Methods 0.000 description 19
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 12
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- 238000010586 diagram Methods 0.000 description 9
- 239000002994 raw material Substances 0.000 description 9
- 241000196324 Embryophyta Species 0.000 description 8
- 238000006477 desulfuration reaction Methods 0.000 description 8
- 230000023556 desulfurization Effects 0.000 description 8
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 6
- 239000003350 kerosene Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 5
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 238000005238 degreasing Methods 0.000 description 4
- 239000003546 flue gas Substances 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 238000004088 simulation Methods 0.000 description 4
- 239000010723 turbine oil Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 150000001342 alkaline earth metals Chemical class 0.000 description 3
- 238000010612 desalination reaction Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 238000005504 petroleum refining Methods 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 229910052720 vanadium Inorganic materials 0.000 description 3
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 3
- 101150076749 C10L gene Proteins 0.000 description 2
- 239000002199 base oil Substances 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000011033 desalting Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000003502 gasoline Substances 0.000 description 2
- 239000003915 liquefied petroleum gas Substances 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000000197 pyrolysis Methods 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 150000003464 sulfur compounds Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 238000010795 Steam Flooding Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000013076 target substance Substances 0.000 description 1
- -1 that is Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 239000002918 waste heat Substances 0.000 description 1
Landscapes
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、ガスタ−ビン発電
の燃料として用いられるガスタ−ビン燃料油、その製造
方法及びガスタービン燃料油を用いた発電方法に関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a gas turbine fuel oil used as a fuel for gas turbine power generation, a method for producing the same, and a power generation method using gas turbine fuel oil.
【0002】[0002]
【従来の技術】一般に石油火力発電においては、原油及
び/または重油をボイラ−の燃料として高圧スチ−ムを
発生させ、これにより蒸気タ−ビンを回して発電を行っ
ている。しかしながらこのシステムは発電効率が低く、
現在高効率大型油焚きボイラ−も開発されているが、発
電効率としては40%前後にとどまっているのが現状
で、大部分のエネルギ−は回収されずに温室ガスとして
放出されている。また同システムからの排ガス中には一
定量のSOX が存在し、排煙脱硫処理はされているもの
の、一部分は大気へ放出され環境への影響が深刻化して
いる。2. Description of the Related Art Generally, in oil-fired power generation, high-pressure steam is generated using crude oil and / or heavy oil as fuel for a boiler, and power is generated by rotating a steam turbine. However, this system has low power generation efficiency,
At present, high-efficiency large oil-fired boilers are also being developed, but at present the power generation efficiency is only around 40%, and most of the energy is released as greenhouse gas without being recovered. In addition, although a certain amount of SOX is present in the exhaust gas from this system, and although flue gas desulfurization treatment has been performed, a part of the exhaust gas is released to the atmosphere and the environmental impact is becoming serious.
【0003】一方、天然ガスを熱源としてガスタ−ビン
を回して発電し、ガスタ−ビンの高温排ガスから排熱を
回収してスチ−ムを発生し、スチ−ムタ−ビンを回して
発電を行うガスタ−ビンコンバインドサイクル発電シス
テムがある。このシステムは発電効率が高くかつ発電単
位当たりのCO2 発生量が少なく、排煙中のSOX 、N
OX の排出量も極めて少ないため、注目されつつある。
ところで天然ガスを原料とすると、ガス田からパイプラ
インで発電設備まで輸送するか、またはLNGを貯蔵、
気化後、ガスタ−ビンで燃焼しなければならず設備コス
トが高いという問題がある。On the other hand, power is generated by turning a gas turbine using natural gas as a heat source, exhaust heat is recovered from high-temperature exhaust gas from the gas turbine, steam is generated, and power is generated by turning the steam turbine. There is a gas turbine combined cycle power generation system. This system has high power generation efficiency and low CO2 emission per power generation unit.
Attention is being paid to OX emissions, which are extremely low.
By the way, if natural gas is used as a raw material, it can be transported from gas fields to power generation facilities by pipeline, or LNG can be stored
After vaporization, it must be burned in a gas turbine, which causes a problem of high equipment cost.
【0004】このようなことから原油を原料としてガス
タ−ビンの燃料油を製造する方法が特開平6−2071
79号公報及び特開平6−209600号公報に記載さ
れている。前者の公報の技術は、塩分含有量を0.5p
pm以下に調整した低硫黄原油を常圧蒸留または減圧蒸
留で分離し、硫黄含有量0.05重量%以下の低沸点留
分からなるガスタ−ビン燃料油を製造する方法である。
また後者の公報の技術は、ガスタービンの排熱を利用し
て低硫黄原油を加熱し、次いでこの低硫黄原油に水素を
作用させ、原油中の硫黄及び重金属の含有量を低減させ
て精製原油を回収し、これをガスタービンの燃料油とす
る方法である。For this reason, a method for producing gas turbine fuel oil using crude oil as a raw material is disclosed in Japanese Patent Application Laid-Open No. 6-2071.
79 and JP-A-6-209600. The technique disclosed in the former publication has a salt content of 0.5 p.
This is a method for producing a gas turbine fuel oil comprising a low-boiling fraction having a sulfur content of 0.05% by weight or less by separating low-sulfur crude oil adjusted to pm or less by atmospheric distillation or vacuum distillation.
Further, the technology of the latter publication uses a waste heat of a gas turbine to heat a low-sulfur crude oil, and then causes hydrogen to act on the low-sulfur crude oil to reduce the content of sulfur and heavy metals in the crude oil to thereby refine the refined crude oil. Is collected and used as fuel oil for gas turbines.
【0005】[0005]
【発明が解決しようとする課題】ところで環境問題から
排煙中の硫黄化合物の量を極力抑えなければならない。
これは排煙脱硫装置を設けることにより解決できるが、
ガスタ−ビン燃料油を用いて発電を行う場合、排煙脱硫
装置を設けると圧力損失により発電効率が低くなってし
まうので、ガスタ−ビン燃料油中の硫黄含有量を極力少
なくすることが好ましい。上述の前者の公報の技術で
は、常圧蒸留または減圧蒸留のみで燃料油を得ているた
め、焚き上げる量がかなり制限されてしまう。従って、
軽質油つまりガスタービン燃料油を多くとることができ
ず、比較的低硫黄である中東原油を用いた場合でも原油
に対し40%台の収率しか得られない。これ以上の収率
を得ようとして焚き上げる量を増やすと、硫黄分が多く
なってしまう。However, due to environmental problems, the amount of sulfur compounds in flue gas must be minimized.
This can be solved by installing a flue gas desulfurization unit,
In the case of generating power using gas turbine fuel oil, if a flue gas desulfurization device is provided, the power generation efficiency will be reduced due to pressure loss. Therefore, it is preferable to minimize the sulfur content in the gas turbine fuel oil. In the technique of the above-mentioned publication, fuel oil is obtained only by atmospheric distillation or vacuum distillation, so that the amount to be heated is considerably limited. Therefore,
Light oil, that is, gas turbine fuel oil cannot be obtained in a large amount, and even when Middle Eastern crude oil having relatively low sulfur is used, a yield of only about 40% with respect to crude oil can be obtained. Increasing the amount to be fired to obtain a higher yield will increase the sulfur content.
【0006】また一般に入手が容易で安価な硫黄含有量
が多い原油に適用した場合には、同じ量の軽質油を回収
すると軽質油中の硫黄含有量が規定値を越え、ガスター
ビン燃料油としては不適確となり回収率はさらに低下せ
ざるを得ず、技術的、経済的に採用することはできな
い。In general, when the present invention is applied to a crude oil which is easily available and inexpensive and has a high sulfur content, if the same amount of light oil is recovered, the sulfur content in the light oil exceeds the specified value, and as a gas turbine fuel oil, Is inaccurate and the recovery rate must be further reduced, and cannot be employed technically and economically.
【0007】一方後者の公報には、メタノールを原料と
して水素を発生し、その水素を利用して原油を水素化精
製する技術が開示されているが、これも低硫黄原油を想
定しているため、硫黄含有量が多い原油に適用するには
限界がある。更に水素化精製の対象が、蒸留した軽質油
ではなく、原油を直接に水素化処理するため、プロセス
条件を原油中の重質油に合わせなくてはならないが、そ
うすると反応温度、圧力を高くし、反応時間(触媒との
接触時間)も長くしなくてはならない。しかしながらこ
の場合原油中の軽質油の分解が進み過ぎてガスタービン
燃料油中にLPG等が多量が含まれ、このためガスター
ビン燃料油を貯留するときに一部がガス化してしまうの
で、ある程度の加圧状態に耐えるタンクが必要になる。
また反応温度、圧力が高いことから、水素化処理を行う
反応容器の構造、材料のコストが高くなる上、反応時間
が長いことから触媒担体部が大きくなって反応容器が大
型化し、触媒の消費量も多くなる。On the other hand, the latter publication discloses a technique for generating hydrogen using methanol as a raw material and hydrorefining crude oil using the hydrogen. However, this technique also assumes a low-sulfur crude oil. However, there is a limit to its application to crude oils with high sulfur content. Furthermore, since the target of hydrorefining is to directly hydrotreat crude oil instead of distilled light oil, the process conditions must be adjusted to the heavy oil in crude oil. Also, the reaction time (contact time with the catalyst) must be increased. However, in this case, the cracking of light oil in the crude oil proceeds too much, and a large amount of LPG and the like is contained in the gas turbine fuel oil. As a result, a part of the gas turbine fuel oil is gasified when the gas turbine fuel oil is stored. A tank that can withstand the pressurization is required.
In addition, the reaction temperature and pressure are high, which increases the cost of the structure and materials of the reaction vessel for performing the hydrogenation treatment.In addition, the reaction time is long, the catalyst support becomes large, the reaction vessel becomes large, and the consumption of the catalyst increases. The amount also increases.
【0008】本発明は、このような事情の下になされた
ものであり、その目的は原料油に対して高い収率でガス
タービン燃料油を得ることのできるガスタ−ビン燃料油
を製造する技術及びその燃料油を用いた発電方法を提供
することを目的とする。The present invention has been made under such circumstances, and an object of the present invention is to provide a technology for producing a gas turbine fuel oil capable of obtaining a gas turbine fuel oil in a high yield relative to a feedstock oil. And a power generation method using the fuel oil.
【0009】[0009]
【課題を解決するための手段】本発明のガスタ−ビン燃
料油の製造方法は、原料油である原油を常圧蒸留して軽
質油と常圧残渣油とに分離する常圧蒸留工程と、この常
圧蒸留工程で得られた軽質油を一括して触媒の存在下で
加圧された水素と接触させて脱不純物処理を行い硫黄濃
度が150ppm以下の精製油を得る第1の水素化処理
工程と、前記常圧残渣油を軽質油と重質油とに分離す
る、減圧蒸留工程、溶剤脱れき工程、熱分解工程及び水
蒸気蒸留工程から選ばれる第1の分離工程と、前記第1
の分離工程にて得られた軽質油を水素化処理することな
く少なくともその一部と前記精製油とを混合してガスタ
−ビン燃料油を得る混合工程と、を含み、この混合工程
で得られたガスタービン燃料油は、粘度が100℃で4
cSt以下、アルカリ金属が1ppm 以下、鉛が1ppm 以
下、Vが0.5ppm以下、Caが2ppm以下、硫黄
が500ppm 以下であることを特徴とする。The method for producing gas turbine fuel oil according to the present invention comprises a normal pressure distillation step in which crude oil as a feedstock is subjected to normal pressure distillation to separate a light oil and a normal pressure residue oil. First light hydrogenation treatment in which the light oil obtained in the atmospheric distillation step is brought into contact with pressurized hydrogen in the presence of a catalyst to remove impurities and obtain a refined oil having a sulfur concentration of 150 ppm or less. A first separation step selected from a vacuum distillation step, a solvent removal step, a pyrolysis step, and a steam distillation step for separating the atmospheric residual oil into light oil and heavy oil;
Mixing the light oil obtained in the separation step without hydrotreating at least a part of the light oil with the refined oil to obtain a gas turbine fuel oil. Gas turbine fuel oil has a viscosity of 4
cSt or less, alkali metal is 1 ppm or less, lead is 1 ppm or less, V is 0.5 ppm or less, Ca is 2 ppm or less, and sulfur is 500 ppm or less.
【0010】この発明では、第1の分離工程にて得られ
た重質油を更に軽質油と重質油とに分離する、溶剤脱れ
き工程及び熱分解工程から選ばれる第2の分離工程を含
み、この第2の分離工程にて得られた軽質油を水素化処
理することなく少なくともその一部と、前記第1の分離
工程にて得られた水素化処理をしない軽質油と、前記精
製油とを混合してガスタ−ビン燃料油を得るようにして
もよい。この発明において原料油における硫黄の含有量
が1.5重量%以下である場合、原料油に対するガスタ
−ビン燃料油の収率60%を越える。[0010] In the present invention, the second separation step, which is selected from a solvent stripping step and a pyrolysis step, for further separating the heavy oil obtained in the first separation step into a light oil and a heavy oil, is carried out. At least a portion of the light oil obtained in the second separation step without hydrotreating, the light oil not subjected to hydrotreatment obtained in the first separation step, Oil may be mixed to obtain gas turbine fuel oil. In the present invention, when the sulfur content in the feedstock is 1.5% by weight or less, the yield of gas turbine fuel oil based on the feedstock exceeds 60%.
【0011】本発明によれば、常圧蒸留工程で得られた
水素化脱硫の容易な軽質油に対して徹底した水素化処理
を行っているので硫黄や金属分をほとんど含まない精製
油が得られ、このため精製油に、常圧残渣に基づいて得
た軽質油を混合しても良質なガスタ−ビン燃料油を得る
ことができる。そして常圧蒸留工程の後に第1の水素化
処理工程を行っているので、常圧蒸留工程では軽質油に
入り込む硫黄や金属分の量を気にせず焚き上げることが
でき、この結果原料油に対して高い収率でガスタ−ビン
燃料油を得ることができる。また目的物がガスタ−ビン
燃料油であるため、第1の水素化処理工程は、常圧蒸留
塔から得られる複数種の軽質油を一括して水素化処理す
れば足り、このようにすることによって設備コストを低
く抑えることができる。According to the present invention, a light oil which is easily subjected to hydrodesulfurization obtained in the atmospheric distillation step is subjected to thorough hydrotreating, so that a purified oil containing almost no sulfur or metal can be obtained. Therefore, even if the refined oil is mixed with the light oil obtained based on the atmospheric residue, a high-quality gas turbine fuel oil can be obtained. And, since the first hydrotreating step is performed after the atmospheric distillation step, the atmospheric distillation step can boil the light oil without worrying about the amount of sulfur and metal components that enter the light oil. On the other hand, gas turbine fuel oil can be obtained with a high yield. In addition, since the target substance is gas turbine fuel oil, the first hydrotreating step only needs to hydrotreat a plurality of types of light oils obtained from the atmospheric distillation column at once. As a result, equipment costs can be kept low.
【0012】こうして得られたガスタ−ビン燃料油の粘
度が100℃で4cSt以下であれば燃焼性が良好であ
るし、金属及び硫黄の含有量が上述のように極微量であ
れば、燃焼温度も例えば1300℃程度と高温燃焼を行
うことができる。If the gas turbine fuel oil thus obtained has a viscosity of 4 cSt or less at 100 ° C., good combustibility is obtained. If the content of metal and sulfur is extremely small as described above, the combustion temperature is low. For example, high-temperature combustion of about 1300 ° C. can be performed.
【0013】更に本発明は、前記第1の分離工程にて得
られた軽質油を触媒の存在下で加圧された水素と接触さ
せて脱不純物処理を行い精製油を得る第2の水素化処理
工程と、前記第1の分離工程にて得られた重質油を更に
軽質油と重質油とに分離する、溶剤脱れき工程及び熱分
解工程から選ばれる第2の分離工程と、を含むように
し、前記第2の分離工程にて得られた軽質油を水素化処
理することなく少なくともその一部と、前記第1の水素
化処理工程にて得られた精製油と、前記第2の水素化処
理工程で得られた精製油とを混合してガスタ−ビン燃料
油を得るようにしてもよい。Further, the present invention provides a second hydrogenation method in which the light oil obtained in the first separation step is brought into contact with pressurized hydrogen in the presence of a catalyst to remove impurities and obtain a purified oil. A treatment step and a second separation step selected from a solvent desorption step and a thermal decomposition step, further separating the heavy oil obtained in the first separation step into a light oil and a heavy oil. And at least a portion of the light oil obtained in the second separation step without hydrotreating, the refined oil obtained in the first hydrotreatment step, and the second oil. May be mixed with the refined oil obtained in the hydrotreating step to obtain a gas turbine fuel oil.
【0014】第1の分離工程の後に第2の水素化処理工
程を行うことにより、第1の分離工程においても硫黄や
金属分の量を気にせず軽質油を多く得ることができるよ
うに処理条件を決めることができ、このため原料油に対
してより高い収率でガスタ−ビン燃料油を得ることが可
能になる。この発明において原料油における硫黄の含有
量が3重量%以下であり、原料油に対するガスタ−ビン
燃料油の収率が70%以上である。なお場合第1の水素
化処理工程と第2の水素化処理工程とは共通化してもよ
い。[0014] By performing the second hydrotreating step after the first separation step, the first separation step can be treated so that a large amount of light oil can be obtained without regard to the amount of sulfur or metal. The conditions can be determined, which makes it possible to obtain gas turbine fuel oil with a higher yield based on the feedstock oil. In the present invention, the sulfur content in the base oil is 3% by weight or less, and the yield of gas turbine fuel oil based on the base oil is 70% or more. In this case, the first hydrotreating step and the second hydrotreating step may be shared.
【0015】以上において本発明は、上述の製造方法
(請求項1ないし6のいずれかに記載の製造方法)によ
り製造されたガスタ−ビン燃料油も権利範囲に含まれ、
更にこのガスタ−ビン燃料油を燃料としてガスタ−ビン
を駆動させて発電を行う工程と、前記ガスタ−ビンから
排出される高温排ガスを排熱回収ボイラ−の熱源とし、
この排熱回収ボイラ−にて発生した蒸気により蒸気タ−
ビンを駆動して発電を行う工程と、を含む発電方法も権
利範囲とするものである。In the above, the present invention also includes gas turbine fuel oil produced by the above-mentioned production method (the production method according to any one of claims 1 to 6).
Further, a step of generating electricity by driving the gas turbine using the gas turbine fuel oil as fuel, and using the high-temperature exhaust gas discharged from the gas turbine as a heat source of an exhaust heat recovery boiler,
The steam generated by the exhaust heat recovery boiler generates steam
The power generation method including the step of driving the bin to generate power is also covered by the rights.
【0016】[0016]
【発明の実施の形態】図1は本発明のガスタ−ビン燃料
油の製造方法を実施するためのシステムを示す説明図で
ある。原料油1としては原油が用いられ、原料油は先ず
脱塩処理部11にて従来の石油精製施設で行われている
条件で脱塩処理される。この処理は、原料油を水と混合
し、水相に塩分、泥分を移行させ、結果としてガスタ−
ビンに悪影響を及ぼすアルカリ金属を除去する。脱塩処
理された原料油は常圧蒸留塔2に送られ、例えば350
℃〜400℃よりも沸点の低い軽質油21と沸点がそれ
を越える残渣油(常圧残渣油)22とに分離される。分
離された軽質油21は第1の水素化処理装置3に送られ
る。DESCRIPTION OF THE PREFERRED EMBODIMENTS FIG. 1 is an explanatory view showing a system for carrying out a method for producing gas turbine fuel oil according to the present invention. Crude oil is used as the feedstock oil 1, and the feedstock oil is first subjected to desalination treatment in the desalination treatment unit 11 under the conditions used in conventional petroleum refining facilities. In this treatment, the raw oil is mixed with water, and the salt and mud are transferred to the aqueous phase.
Removes alkali metals that have an adverse effect on bottles. The desalted raw material oil is sent to the atmospheric distillation column 2 and, for example, 350
It is separated into a light oil 21 having a boiling point lower than 400 ° C and a residual oil (normal pressure residual oil) 22 having a boiling point higher than that. The separated light oil 21 is sent to the first hydrotreating apparatus 3.
【0017】ここで一般の石油精製施設の常圧蒸留塔2
においては、軽質油の中で沸点の高いものから低いもの
まであるため、灯油、ガソリンなどといった具合に、い
くつかの沸点領域毎に留分を取り出し、塔の上部から下
方に亘って順に留分の取り出し口を設け、夫々の取り出
し口から目的とする軽質油を取り出しているが、この実
施の形態では例えば塔頂部から軽質油を一括して取り出
し、つまり各留分が混合している状態で取り出し、水素
化処理装置に送っている。ただし図2に示す如く、一般
の常圧蒸留塔2のように複数の取り出し口から各沸点領
域の留分を取り出し(図2の例では4つの取り出し口か
ら取り出している)、これらを合流して水素化処理装置
3に送り、ここで一括して水素化処理を行ってもよい。Here, the atmospheric distillation column 2 of a general petroleum refining facility
, Since light oils have a high boiling point to a low boiling point, distillates are taken out at every boiling point region, such as kerosene, gasoline, etc. Are provided, and light oils of interest are taken out from the respective outlets.In this embodiment, for example, light oil is taken out at once from the top of the tower, that is, in a state where each fraction is mixed. Removed and sent to the hydrotreating unit. However, as shown in FIG. 2, fractions of each boiling point region are taken out from a plurality of outlets as in a general atmospheric distillation column 2 (in the example of FIG. 2, they are taken out from four outlets), and they are combined. May be sent to the hydrotreating device 3 where the hydrotreating may be performed collectively.
【0018】この点について更に述べると、一括脱硫自
動車燃料油製造の場合、ガソリン、灯油、軽油の各々で
脱硫のレベルが異なり、温度、圧力、触媒などの運転操
作条件が異なる。一方沸点が例えば350℃よりも低い
軽質油を一括して脱硫しガスタ−ビン燃料油を製造する
場合には、全体としてガスタ−ビン燃料油の仕様に合致
すればよく、各運転条件などは製油所での条件とはかな
り異なるものである。従って既述のように常圧蒸留塔2
からの軽質油を一括してつまり共通の装置で水素化処理
を行うことができる。To further explain this point, in the case of batch desulfurization automobile fuel oil production, each of gasoline, kerosene and light oil has a different level of desulfurization, and operating conditions such as temperature, pressure and catalyst are different. On the other hand, in the case of producing gas turbine fuel oil by batch desulfurization of light oil having a boiling point of, for example, lower than 350 ° C., the gas turbine fuel oil only needs to conform to the specifications of the gas turbine fuel oil. It is quite different from the local conditions. Therefore, as described above, the atmospheric distillation column 2
Can be subjected to hydrogenation at once, that is, with a common device.
【0019】即ち常圧蒸留プロセスでは沸点の異なる複
数種の軽質油が得られるが、目的物がガスタービン燃料
油であるから、これらの軽質油を一括して水素化処理装
置で処理することができ、このように一括処理を行うこ
とにより設備のコストを低く抑えることができる。また
本発明システムで適用する水素化処理技術は自動車燃料
を生産する製油所での水素化処理工程とは異なり、例え
ば自動車燃料油では水素化時の油の着色が問題となり、
それを抑えるため低温、高圧で運転するが、ガスタ−ビ
ン燃料油では色相でも問題がないため、高温運転が可能
となり、従って低圧運転による反応器のコストの削減が
可能となり、この点からも設備コストを低く抑えること
ができる。That is, in the atmospheric distillation process, a plurality of types of light oils having different boiling points can be obtained. However, since the target product is a gas turbine fuel oil, these light oils can be collectively processed by a hydrotreating apparatus. It is possible to reduce the cost of the equipment by performing the batch processing in this manner. Also, the hydrotreating technology applied in the system of the present invention is different from the hydrotreating process in a refinery that produces automobile fuel. For example, in automobile fuel oil, coloring of oil during hydrogenation becomes a problem,
In order to suppress this, low-temperature and high-pressure operation is performed. However, gas turbine fuel oil has no problem with hue, so that high-temperature operation is possible. Therefore, reactor cost can be reduced by low-pressure operation. Costs can be kept low.
【0020】続いて水素化処理装置3及びその工程(第
1の水素化処理工程)について図3を参照しながら述べ
ると、軽質油21は、加圧された水素ガスと混合され、
反応塔31の上部から反応塔31内に供給される。反応
塔31内には担体に触媒を担持した触媒層32が設けら
れ、軽質油21及び水素ガスはこの触媒層32を通過し
て反応塔31の底部から送液管33を介して高圧タンク
34内に流入する。軽質油21に含まれるつまり炭化水
素分子の中に入り込んでいる微量のバナジウム、ニッケ
ル、鉛等の重金属類(金属分は主に重質油に含まれてい
るため極微量である)と、硫黄及び窒素とは、軽質油2
1及び水素ガスが触媒層32を通過するときに水素と反
応して、炭化水素分子から脱離し、金属分は触媒表面に
吸着され、硫黄や窒素は水素と反応して夫々硫化水素、
アンモニアとなる。またアルカリ金属は油分中に含まれ
る若干の水分中に溶けているかまたは塩の形で存在する
が、触媒表面で吸着される。Next, the hydrotreating apparatus 3 and its steps (first hydrotreating step) will be described with reference to FIG. 3. Light oil 21 is mixed with pressurized hydrogen gas,
It is supplied into the reaction tower 31 from the upper part of the reaction tower 31. A catalyst layer 32 having a catalyst carried on a carrier is provided in the reaction tower 31, and the light oil 21 and the hydrogen gas pass through the catalyst layer 32 and pass through a liquid feed pipe 33 from the bottom of the reaction tower 31 to a high-pressure tank 34. Flows into. A small amount of heavy metals such as vanadium, nickel, lead and the like contained in the light oil 21, that is, in the hydrocarbon molecule (the metal component is mainly contained in the heavy oil and is very small), and sulfur And nitrogen are light oil 2
When 1 and hydrogen gas pass through the catalyst layer 32, they react with hydrogen to be desorbed from hydrocarbon molecules, metal components are adsorbed on the catalyst surface, and sulfur and nitrogen react with hydrogen to react with hydrogen sulfide,
It becomes ammonia. The alkali metal is dissolved in some water contained in the oil or exists in the form of a salt, but is adsorbed on the catalyst surface.
【0021】そして反応塔31の底部からは高圧ガスと
油との混合流体が排出され、高圧タンク34にて水素ガ
スが分離される。水素ガスはコンプレッサCPにより昇
圧されて反応塔31内に循環供給される。一方高圧タン
ク34にて分離された液体分は圧力調整弁PVを介して
低圧タンク35内に送られ、圧力が例えば10%〜30
%程度低下し、このため液体(油)中に溶けている硫化
水素やアンモニアなどの溶解ガスが気化する。こうして
分離された液体つまり精製油はガスタービン燃料油とな
る。35aはポンプである。また低圧タンク35で分離
されたガス中には、未反応の水素ガスの他に、硫化水
素、アンモニア等の水素化された化合物が含まれ、更に
炭化水素分子の一部が切れて生成されたメタン、液化石
油ガス留分から軽質ナフサまでの軽質油(ここでいう軽
質油は前記軽質油21に対して更なる軽質な成分であ
る。)も含まれている。前記タンク35にて分離された
ガスは、不純物除去部36にて、そのガスに含まれてい
る硫化水素、アンモニア、が除去される。不純物除去部
36は例えば硫化水素やアンモニアを吸収するための吸
収液の塔を設け、この中にガスを通すことによって不純
物が除去される。こうして不純物が除去されたガスは、
未反応のメタン、エタンなどの炭素数の少ない軽質油の
混合ガスであり、この混合ガス42を水素プラント4に
送り、混合ガス42中の軽質油を水素ガスの製造原料と
し用いる。なお常圧蒸留2で分離された軽質油21の一
部も水素プラントに送り、水素ガスの製造原料として用
いる。また水素ガスの製造原料を重油に限定する場合に
は、始動時のみ外部からナフサを導入して運転する場合
もある。A mixed fluid of high-pressure gas and oil is discharged from the bottom of the reaction tower 31, and hydrogen gas is separated in a high-pressure tank 34. The hydrogen gas is pressurized by the compressor CP and circulated and supplied into the reaction tower 31. On the other hand, the liquid separated in the high-pressure tank 34 is sent into the low-pressure tank 35 through the pressure regulating valve PV, and the pressure is, for example, 10% to 30%.
%, So that dissolved gases such as hydrogen sulfide and ammonia dissolved in the liquid (oil) evaporate. The liquid thus separated, that is, refined oil, becomes gas turbine fuel oil. 35a is a pump. The gas separated in the low-pressure tank 35 contains hydrogenated compounds such as hydrogen sulfide and ammonia, in addition to unreacted hydrogen gas, and is further generated by cutting off a part of hydrocarbon molecules. Light oils from methane and liquefied petroleum gas fractions to light naphtha (light oil is a lighter component relative to the light oil 21) are also included. From the gas separated in the tank 35, hydrogen sulfide and ammonia contained in the gas are removed in the impurity removing section 36. The impurity removing section 36 is provided with, for example, a tower of an absorbing solution for absorbing hydrogen sulfide and ammonia, and the impurities are removed by passing gas through the tower. The gas from which impurities have been removed is
It is a mixed gas of light oil having a small number of carbon atoms, such as unreacted methane and ethane. The mixed gas 42 is sent to the hydrogen plant 4, and the light oil in the mixed gas 42 is used as a raw material for producing hydrogen gas. A part of the light oil 21 separated by the atmospheric distillation 2 is also sent to the hydrogen plant and used as a raw material for producing hydrogen gas. When the raw material for producing hydrogen gas is limited to heavy oil, the operation may be performed by introducing naphtha from the outside only at the time of starting.
【0022】一方既述のように反応塔31に供給される
水素ガスは循環して使用されるが、この循環路37のガ
ス中の水素ガスは次第に減少し、一方メタンなどの軽質
油は次第に増加する。このため水素ガスの割合が少なく
なるのを防ぐため水素プラント4から循環路37に水素
ガス41を補充し、水素化処理が確実に行われるように
している。On the other hand, as described above, the hydrogen gas supplied to the reaction tower 31 is circulated and used, but the hydrogen gas in the gas in the circulation path 37 gradually decreases, while the light oil such as methane gradually decreases. To increase. Therefore, in order to prevent the ratio of the hydrogen gas from decreasing, the hydrogen gas 41 is replenished from the hydrogen plant 4 to the circulation path 37, so that the hydrogenation process is reliably performed.
【0023】図4は水素プラント4の要部を示す図であ
る。この水素プラント4は燃料ガスを燃焼する燃焼炉4
3の中に反応管44を設けてなり、メタンなどの軽質油
と水蒸気とを反応管44の中に通し、軽質油を水蒸気改
質して水素を生成すると共に一酸化炭素を副生成する。
そしてこのガスから一酸化炭素を除去し、水素ガスを得
る。ここで行われる除去処理(精製)については、例え
ばPSA(圧力変動吸着分離法)、TSA(温度変動吸
着分離法)、深冷分離法または膜分離法などを用いるこ
とができる。FIG. 4 is a diagram showing a main part of the hydrogen plant 4. This hydrogen plant 4 has a combustion furnace 4 for burning fuel gas.
3, a light pipe such as methane and steam are passed through the reaction pipe 44, and the light oil is steam-reformed to produce hydrogen and by-produced carbon monoxide.
Then, carbon monoxide is removed from this gas to obtain hydrogen gas. For the removal treatment (purification) performed here, for example, PSA (pressure fluctuation adsorption separation method), TSA (temperature fluctuation adsorption separation method), cryogenic separation method, membrane separation method, or the like can be used.
【0024】ここで本発明の第1の水素化処理工程及び
後述の実施の形態にて行われる第2の水素化処理工程
は、触媒の存在下で加圧された水素と接触させ、硫黄化
合物など不純物の除去を行う水素化脱硫を主な目的とし
ている。Here, in the first hydrotreating step of the present invention and the second hydrotreating step performed in the embodiment described later, the sulfur compound is brought into contact with pressurized hydrogen in the presence of a catalyst. Its main purpose is hydrodesulfurization to remove impurities.
【0025】第1の水素化処理装置3で行われるプロセ
ス(第1の水素化処理工程)について述べると、従来の
石油精製では、軽質油留分中のナフサ、灯軽油等を別々
に対象にして狭い沸点範囲の留分を水素化処理している
のに対し、本発明では常圧蒸留で蒸留された留分のすべ
てを一括して水素化処理する。従って水素化処理量が大
幅に増加し、従来とは大きく異なる。水素化処理の水素
ガスの圧力、反応温度等の条件については油種、目的精
製度等に応じて温度340から420℃、水素ガスの圧
力30kg/cm2〜80kg/cm2、LHVS(liqu
id hourly space velocity)0.5〜6hr-1で選択で
き、精製油の硫黄濃度を150ppm以下とすることが
好ましい。また、触媒は従来公知の水素化処理触媒を任
意に選択できるが、Ni、Mo、Coの硫化物をアルミ
ナに担持した触媒が好ましい。この様な技術は、自動車
用軽油の超深度脱硫レベル(50ppm)達成に向け開
発されつつある技術であり、本発明では当該技術を応用
し、ナフサから灯軽油までの広範囲留出油で種々の油種
において30〜150ppmの超深度脱硫を実施するも
のである。The process (first hydrotreating step) performed in the first hydrotreating apparatus 3 will be described. In the conventional petroleum refining, naphtha, kerosene light oil, and the like in a light oil fraction are separately targeted. In contrast, in the present invention, all the fractions distilled by atmospheric distillation are subjected to the hydrotreating at once. Therefore, the amount of hydrotreating is greatly increased, which is greatly different from the conventional case. The conditions such as the pressure of hydrogen gas and the reaction temperature of the hydrogenation treatment are 340 to 420 ° C., the pressure of hydrogen gas is 30 kg / cm 2 to 80 kg / cm 2, and the LHVS (liqu
(id hourly space velocity) can be selected from 0.5 to 6 hr-1 and the sulfur concentration of the refined oil is preferably set to 150 ppm or less. As the catalyst, a conventionally known hydrotreating catalyst can be arbitrarily selected, but a catalyst in which sulfides of Ni, Mo, and Co are supported on alumina is preferable. Such a technique is a technique being developed to achieve an ultra-deep desulfurization level (50 ppm) of a light oil for automobiles. In the present invention, various techniques are applied to a wide range of distillate oils from naphtha to kerosene light oil by applying the technique. This is to carry out ultra-deep desulfurization of 30 to 150 ppm in the oil type.
【0026】一方前記常圧蒸留塔2で分離された残渣油
(常圧残渣油)22は第1の分離工程により分離処理さ
れ軽質油と重質油とに分離される。この分離工程として
は例えば減圧蒸留工程を挙げることができる。この場合
前記残渣油は減圧蒸留塔5に送られここで常圧残渣油の
中でも軽い成分である、例えば常圧沸点で565℃より
も低い軽質油(減圧軽質油)51と、重い成分である、
常圧沸点がそれを越える重質油(減圧残渣油)52とに
分離される。On the other hand, the residual oil (normal pressure residual oil) 22 separated in the atmospheric distillation column 2 is separated in a first separation step and separated into light oil and heavy oil. This separation step can be, for example, a vacuum distillation step. In this case, the residual oil is sent to the vacuum distillation column 5 where it is a light component among the atmospheric residual oils, for example, a light oil (low-pressure light oil) 51 whose boiling point at normal pressure is lower than 565 ° C. and a heavy component. ,
It is separated into heavy oil (vacuum residual oil) 52 whose boiling point exceeds normal pressure.
【0027】軽質油51は水素化処理されることなく、
少なくともその一部と前記第1の水素化処理工程3にて
得られた精製油30と混合され(混合工程)、ガスタ−
ビン燃料油となる。混合比率は原料油により異なるが、
ガスタービン燃料油の性状について、粘度が100℃で
4cSt以下、アルカリ金属が1ppm 以下、鉛が1ppm
以下、Vが0.5ppm以下、Caが2ppm以下、硫
黄が500ppm 以下となるように混合される。なお重質
油(減圧残渣油)52は必要に応じて粘度調整された
後、重油原料あるいはボイラー燃料油として利用する。The light oil 51 is not hydrotreated.
At least a part thereof is mixed with the refined oil 30 obtained in the first hydrotreating step 3 (mixing step),
It becomes bottle fuel oil. The mixing ratio depends on the feedstock,
Regarding the properties of gas turbine fuel oil, viscosity is 4 cSt or less at 100 ° C, alkali metal is 1 ppm or less, lead is 1 ppm
Hereinafter, mixing is performed so that V is 0.5 ppm or less, Ca is 2 ppm or less, and sulfur is 500 ppm or less. The heavy oil (vacuum residue) 52 is used as a heavy oil feedstock or boiler fuel oil after its viscosity is adjusted as required.
【0028】上述実施の形態によれば、常圧蒸留工程の
後に水素化処理を行っているので硫黄や重金属の量を気
にせず上に焚き上げることができるため、常圧蒸留工程
にて深絞りをすることができ、結果として硫黄がほとん
ど含まれない精製油を多く得ることができる。一方減圧
蒸留を経て得られた軽質油51は水素化処理をしていな
いので硫黄濃度が高いため、その硫黄濃度に応じて当該
軽質油51の量を調整して精製油30に混合することに
より、既述の成分規定を満足するガスタ−ビン燃料油が
得られる。According to the above-described embodiment, since the hydrogenation treatment is performed after the atmospheric pressure distillation step, it is possible to heat up without worrying about the amount of sulfur or heavy metal. Squeezing can be performed, and as a result, a large amount of refined oil containing almost no sulfur can be obtained. On the other hand, since the light oil 51 obtained through the vacuum distillation has not been subjected to hydrogenation treatment and has a high sulfur concentration, the amount of the light oil 51 is adjusted according to the sulfur concentration, and the light oil 51 is mixed with the refined oil 30. Thus, a gas turbine fuel oil satisfying the above-mentioned component rules can be obtained.
【0029】また常圧残渣油から分離した軽質油51に
ついては水素化処理を行わずに少なくともその一部を精
製油30に混合していることから水素化処理装置3とし
ては第1の水素化処理のためのものだけでよいので設備
コストを低く抑えることができる。なお後述のように軽
質油51を第1の水素化処理装置3に供給する例と比較
した場合、水素化処理条件を軽質油51の性状に合わせ
込まなくてはならないので温度、圧力等の反応条件が厳
しくなることから、設備コストという点については図1
の実施の形態の方が有利である。ガスタービン燃料油の
収率については、原料油として硫黄濃度が0.8重量%
未満と低い低硫黄原油を用いた場合、70重量%以上の
収率が得られる。また原料油の硫黄濃度が0.8重量%
以上、1.5重量%以下の場合には60重量%を越えた
収率が得られる。Since the light oil 51 separated from the normal pressure residual oil is not subjected to the hydrotreating but at least a part thereof is mixed with the refined oil 30, the first hydrotreating apparatus 3 is used as the hydrotreating apparatus 3. Equipment costs can be kept low because only processing is required. In addition, when compared with the example in which the light oil 51 is supplied to the first hydrotreating apparatus 3 as described later, since the hydrotreating conditions must be adjusted to the properties of the light oil 51, the reaction of temperature, pressure, etc. Due to the stricter conditions, the cost of equipment is
The embodiment is more advantageous. Regarding the yield of gas turbine fuel oil, the sulfur concentration of the feed oil was 0.8% by weight.
If low sulfur crudes are used, a yield of 70% by weight or more is obtained. The sulfur concentration of the feedstock is 0.8% by weight.
As described above, when the content is 1.5% by weight or less, a yield exceeding 60% by weight is obtained.
【0030】また原油をそのまま水素化処理するのでは
なく、蒸留工程の後に軽質油に対して水素化処理を行う
ので、反応条件は軽質油に合わせればよく、従って反応
圧力、温度はそれ程高くしなくて済むし、反応時間も短
くて済み、設備がその分簡素化できる。更にガスタービ
ン燃料油を目的としているので既述したように蒸留工程
で得られた各留分に対して水素化処理を行うことなく、
これらを一括して水素化処理でき、こうしたことから水
素化処理を行っているとはいっても、全体としては簡単
なプロセスで行うことができる。Since the crude oil is not hydrotreated as it is, but the light oil is hydrotreated after the distillation step, the reaction conditions may be adjusted to that of the light oil. It is not necessary, the reaction time is short, and the equipment can be simplified accordingly. Further, since it is intended for gas turbine fuel oil, as described above, without performing hydrotreating on each fraction obtained in the distillation step,
These can be subjected to hydrogenation at once, and thus hydrogenation can be performed by a simple process as a whole even though hydrogenation is performed.
【0031】本発明は、常圧蒸留装置2の残渣油22を
分離する第1の分離工程を行う手法としては、減圧蒸留
に限らず水蒸気蒸留法、溶剤脱れき法、あるいは残渣油
22を例えば430〜490℃まで加熱して熱エネルギ
ーにより炭化水素分子を切断して軽質油と重質油とを得
る熱分解法などであってもよい。In the present invention, the method of performing the first separation step of separating the residual oil 22 of the atmospheric distillation apparatus 2 is not limited to vacuum distillation, but may be, for example, a steam distillation method, a solvent removal method, or a method of removing the residual oil 22. For example, a thermal decomposition method of heating to 430 to 490 ° C. and cutting hydrocarbon molecules by thermal energy to obtain light oil and heavy oil may be used.
【0032】また本発明は、例えば原料油の硫黄濃度が
0.5重量%以下と低い場合第1の分離工程で得られた
重質油を更に第2の分離工程で軽質油と重質油とに分離
し、その軽質油を前記精製油及び軽質油51に混合して
(混合工程)ガスタービン燃料油を得るようにしてもよ
い。図5はこのような実施の形態を示す図であり、第1
の分離工程として減圧蒸留を行い、その重質分(減圧残
渣油)52に対して、第2の分離工程である溶剤脱れき
(溶剤抽出)工程を行う例を示している。The present invention also relates to a method for producing heavy oil obtained in the first separation step when the sulfur concentration of the feedstock oil is as low as 0.5% by weight or less. And the light oil is mixed with the refined oil and the light oil 51.
(Mixing Step) Gas turbine fuel oil may be obtained. FIG. 5 is a diagram showing such an embodiment.
Vacuum distillation is carried out as a separation step, and the heavy fraction (vacuum residue oil) 52 is subjected to solvent removal as a second separation step.
An example is shown in which a (solvent extraction) step is performed.
【0033】減圧蒸留塔5で分離された重質油(減圧残
渣油)52は、溶剤脱れき装置(溶剤抽出装置)6で軽
質油である脱れき油61と重質油である脱れき残渣油6
2とに分離される。この分離は、例えば塔の上部及び下
部から夫々減圧残渣油52及び溶剤を供給してこれらを
向流接触させ、減圧残渣油52中の軽質油と重質油とを
溶剤に対する溶解度の違いにより分離することによって
行われる。The heavy oil (vacuum residue oil) 52 separated in the vacuum distillation column 5 is separated by a solvent degreasing unit (solvent extraction unit) 6 into a degreasing oil 61 which is a light oil and a degreasing residue which is a heavy oil. Oil 6
And 2. In this separation, for example, the vacuum residue 52 and the solvent are supplied from the upper and lower portions of the column, respectively, and they are brought into countercurrent contact with each other, and light oil and heavy oil in the vacuum residue 52 are separated by the difference in solubility in the solvent. It is done by doing.
【0034】分離された脱れき油(軽質油)61の少な
くとも一部は前記減圧蒸留塔5からの軽質油51及び前
記精製油30と混合されてガスタービン燃料油として利
用する。脱れき残渣油62は必要に応じて粘度調整され
た後、重油原料あるいはボイラー燃料油として利用す
る。なお第2の分離工程は既述の熱分解工程であっても
よい。そしてまた本発明は、原料油の硫黄濃度が例えば
1.7重量%と高い場合には図5の実施の形態におい
て、図6に示すように減圧蒸留塔5の後段に第2の水素
化処理装置7を設置し、軽質油51(減圧軽油)をこの第
2の水素化処理装置7に送って水素化処理装置(第2の
水素化処理工程)を行い、水素化処理された精製油70
を第2の分離工程で得られた例えば軽質油61の少なく
とも一部と前記精製油30と混合し(混合工程)、ガスタ
ービン燃料油として用いてもよい。At least a part of the separated deoiled oil (light oil) 61 is mixed with the light oil 51 from the vacuum distillation column 5 and the refined oil 30 and used as a gas turbine fuel oil. After the viscosity of the removed residual oil 62 is adjusted as required, it is used as a heavy oil feedstock or a boiler fuel oil. Note that the second separation step may be the above-described thermal decomposition step. Further, according to the present invention, when the sulfur concentration of the feed oil is as high as 1.7% by weight, for example, in the embodiment of FIG. 5, as shown in FIG. The apparatus 7 is installed, and the light oil 51 (decompressed light oil) is sent to the second hydrotreating apparatus 7 to perform the hydrotreating apparatus (second hydrotreating step), and the refined oil 70 that has been hydrotreated
May be mixed with at least a part of, for example, the light oil 61 obtained in the second separation step and the refined oil 30 (mixing step) and used as a gas turbine fuel oil.
【0035】このような実施の形態によれば、軽質油5
1(減圧軽油)についても水素化処理を行っているので、
第2の分離工程で得られた例えば軽質油61については
水素化処理を行わなくとも、前記精製油30,70と混
合することにより硫黄濃度が規定値に入るガスタ−ビン
燃料油を高い収率で得ることができる。この場合ガスタ
ービン燃料油の収率については、原料油として硫黄濃度
が2重量%未満と低い低硫黄原油を用いた場合、80重
量%以上の収率が得られる。また原料油の硫黄濃度が2
重量%以上、3重量%以下の場合には70重量%以上の
収率が得られる。According to such an embodiment, the light oil 5
1 (decompressed gas oil) is also hydrotreated,
For example, with respect to the light oil 61 obtained in the second separation step, the gas turbine fuel oil having a sulfur concentration falling within a specified value can be obtained at a high yield by mixing with the refined oils 30 and 70 without performing the hydrogenation treatment. Can be obtained at In this case, the yield of the gas turbine fuel oil is 80% by weight or more when a low sulfur crude oil having a low sulfur concentration of less than 2% by weight is used as a feed oil. Also, if the sulfur concentration of the feed oil is 2
When the amount is from 3% by weight to 3% by weight, a yield of 70% by weight or more is obtained.
【0036】第2の水素化処理装置7における水素ガス
の圧力、反応温度等の条件については油種、目的精製度
等に応じて温度360から420℃、水素ガスの圧力3
0kg/cm2〜100kg/cm2、LHVS(liquid
hourly space velocity)0.1〜3hr-1で選択で
き、精製油の硫黄濃度を例えば500ppm以下とする
ことが好ましい。また本発明は、例えば図6の実施の形
態のように常圧蒸留塔2で得られた軽質油21と減圧蒸
留塔5で得られた軽質油(減圧軽質油)51とを別々の
水素化処理装置で処理する代わりに、図7に示すように
これらを混合して同じ水素化処理装置8で水素化処理を
行ってもよい。つまりこの場合第1の水素化処理装置3
及び第2の水素化処理装置7を共通化したことになる。
一般に水素化処理の反応条件は原料中の重質油に併せて
設定し、この例では重質油は軽質油(減圧軽質油)51
に相当する。従って原料中の軽質油21と減圧軽質油5
1との重量比(容量比)において、軽質油21の割合を
低くしてこれらを一括して処理することにより軽質油水
素化処理装置を省くことができ、コストを削減できる。
なお軽質油21の割合が高いと(つまり減圧軽質油51
の割合が低いと)、反応条件を少量の重質油(減圧軽質
油51に相当する)に合わせて設定するため反応器設計
値が厳しくなり、経済効果がでにくい。これに対して減
圧軽質油51に反応条件を合わせて精製すれば軽質油の
精製度は大幅に向上する。また減圧蒸留塔5で得られた
軽質油51を水素化処理する場合、図6および図7に点
線で示したように減圧蒸留塔5に重油を供給してもよ
い。このような供給は、本発明である常圧蒸留塔2に原
油を供給して行われる一連の工程に影響を与えるもので
はない。上述のようにして得られた混合油(ガスタービ
ン油)は、図示しない常圧蒸留圧塔で例えば350℃で
蒸留して、軽質なガスタ−ビン燃料油と、それよりは重
質なガスタ−ビン燃料油とを得るようにしてもよい。本
発明では、既述の第1の分離工程及び/または第2の分
離工程で得られた重質油を酸素ガスにより部分酸化して
水素を生成し、その水素を水素化処理装置で使用するよ
うにしてもよい。本発明で得られたガスタ−ビン燃料油
は例えば発電に利用することができ、その例を図8に示
す。ガスタ−ビン燃料油は、燃焼ノズルで燃焼されてそ
の燃焼ガスによりガスタ−ビン201が駆動され、発電
機202から電力が取り出される。一方このガスタ−ビ
ン201から排出された高温排ガスは排熱回収ボイラ2
03に供給され、排ガスの熱によりスチ−ムを発生させ
る。このスチ−ムによりスチ−ムタ−ビン204が駆動
され、発電機205から電力が取り出される。このよう
にして発電を行えば、ガスタ−ビン燃料油の排熱が有効
利用でき、効率の高い発電を行うことができる。The conditions such as the pressure of hydrogen gas, the reaction temperature and the like in the second hydrotreating apparatus 7 are from 360 ° C. to 420 ° C. and the pressure of hydrogen gas 3
0kg / cm2 ~ 100kg / cm2, LHVS (liquid
hourly space velocity) can be selected from 0.1 to 3 hr -1, and the sulfur concentration of the refined oil is preferably, for example, 500 ppm or less. Further, the present invention provides a method for separately hydrogenating the light oil 21 obtained in the atmospheric distillation column 2 and the light oil (decompressed light oil) 51 obtained in the vacuum distillation column 5 as in the embodiment of FIG. Instead of processing with a processing device, these may be mixed and subjected to hydrogenation in the same hydroprocessing device 8 as shown in FIG. That is, in this case, the first hydrotreating apparatus 3
This means that the second hydrotreating apparatus 7 is shared.
Generally, the reaction conditions for the hydrotreating are set in accordance with the heavy oil in the feedstock. In this example, the heavy oil is light oil (reduced light oil) 51.
Is equivalent to Therefore, the light oil 21 and the reduced light oil 5
By reducing the ratio of the light oil 21 to the weight ratio (capacity ratio) to 1 and treating them collectively, the light oil hydrotreating apparatus can be omitted, and the cost can be reduced.
If the ratio of the light oil 21 is high (that is, the reduced light oil 51
Is low), the reaction conditions are set in accordance with a small amount of heavy oil (corresponding to the reduced pressure light oil 51), so that the design value of the reactor becomes strict and the economic effect is hardly obtained. On the other hand, if the refined light oil 51 is refined in accordance with the reaction conditions, the refining degree of the light oil is greatly improved. When the light oil 51 obtained in the vacuum distillation column 5 is subjected to hydrogenation treatment, heavy oil may be supplied to the vacuum distillation column 5 as shown by a dotted line in FIGS. 6 and 7. Such a supply does not affect a series of steps performed by supplying the crude oil to the atmospheric distillation column 2 of the present invention. The mixed oil (gas turbine oil) obtained as described above is distilled at, for example, 350 ° C. in an atmospheric pressure distillation column (not shown) to produce a light gas turbine fuel oil and a heavier gas turbine fuel oil. Bottle fuel oil may be obtained. In the present invention, the heavy oil obtained in the above-described first separation step and / or second separation step is partially oxidized with oxygen gas to generate hydrogen, and the hydrogen is used in a hydrotreating apparatus. You may do so. The gas turbine fuel oil obtained by the present invention can be used, for example, for power generation, and an example is shown in FIG. The gas turbine fuel oil is burned by a combustion nozzle, and the combustion gas drives the gas turbine 201, so that electric power is extracted from the generator 202. On the other hand, the high-temperature exhaust gas discharged from the gas turbine 201 is discharged to the exhaust heat recovery boiler 2.
03 and generates steam by the heat of the exhaust gas. The steam drives the steam turbine 204 to extract power from the generator 205. If power is generated in this manner, the exhaust heat of the gas turbine fuel oil can be effectively used, and power generation can be performed with high efficiency.
【0037】(実施例1)図1に示す本発明でのプロセ
スによりUAEのMurban原油(硫黄濃度:0.7
8wt%)によりタービン油製造を試みた。100重量
単位の原油は脱塩工程を経た後、常圧蒸留工程で沸点が
380℃よりも低い軽質油(75重量単位)と沸点がそ
れより高い重質油(25重量単位)とに分離し、第1の
水素化処理工程における水素ガスの圧力を50kg/c
m2、LHSV 1hr-1に設定し、硫黄濃度60pp
mの深度脱硫精製油を得た。また第1の分離工程である
減圧蒸留工程では沸点(常圧時の沸点)が480℃より
も低い硫黄濃度8500ppmの軽質油(4重量単位)
と沸点がそれよりも高い重質油とに分離した。この減圧
蒸留工程で得られた軽質油と第1の水素化処理で得られ
たガスタービン燃料油と混合した。ガスタービン燃料油
全体として、回収率は79重量単位となり、アルカリ金
属、アルカリ土類金属、バナジウム、鉛は検出されず、
硫黄濃度において490ppm、粘度は100℃で0.
4cStのガスタービン燃料油製造が可能となった。(Example 1) The UAE Murban crude oil (sulfur concentration: 0.7
(8% by weight). After 100 weight units of crude oil undergoes a desalting process, it is separated into a light oil (75 weight units) having a boiling point lower than 380 ° C and a heavy oil (25 weight units) having a higher boiling point by an atmospheric distillation process. The pressure of the hydrogen gas in the first hydrotreating step is 50 kg / c
m2, LHSV 1hr-1 and sulfur concentration 60pp
m deep desulfurized refined oil was obtained. In the first distillation step, a vacuum distillation step, a light oil having a boiling point (boiling point at normal pressure) having a sulfur concentration of 8500 ppm lower than 480 ° C. (4 weight units)
And heavy oil having a higher boiling point. The light oil obtained in this vacuum distillation step was mixed with the gas turbine fuel oil obtained in the first hydrotreating. As a whole gas turbine fuel oil, the recovery rate is 79 weight units, and no alkali metal, alkaline earth metal, vanadium, and lead are detected.
The sulfur concentration is 490 ppm and the viscosity is 0.1 at 100 ° C.
Production of 4 cSt gas turbine fuel oil has become possible.
【0038】原油からのエネルギーは全て電力(ガスタ
ービン及びボイラー発電)に転換するとしてシミュレー
ションを実施した。尚精製プラントでの所内消費率は4
%とし、コンバインドサイクルガスタービン発電効率4
9%、ボイラー発電効率38%に設定した。以上の条件
下において精製プラントへの原油供給を熱量換算で10
0単位とし、最終的な電力回収量を算定したところ、熱
量換算において45.2単位の電力エネルギー回収が可
能となった。The simulation was performed assuming that all the energy from the crude oil was converted to electric power (gas turbine and boiler power generation). The internal consumption rate at the refinery plant is 4
%, Combined cycle gas turbine power generation efficiency 4
9% and boiler power generation efficiency were set to 38%. Under the above conditions, supply of crude oil to the refinery plant
When the final power recovery amount was calculated using 0 units, it was possible to recover 45.2 units of power energy in terms of calorific value.
【0039】(比較例1)実施例1と同様にUAEのM
urban原油を用い、特開平6−207179により
ガスタービン燃料油を製造した。同報では塩分濃度を
0.5ppm以下に調整した低硫黄原油を原料とし、蒸
留法により硫黄濃度が0.05wt%以下のガスタービ
ン燃料油を製造するとしている。ガスタービン燃料油
は、沸点領域230℃までの軽質ナフサから灯油留分に
限られ、アルカリ金属、アルカリ土類金属、V及び鉛は
検出されず、硫黄濃度はおよそ490ppm、粘度は1
00℃で0.1cStと高品質であったが、原料油に対
するガスタービン燃料油の収率は39%と低い回収率で
あった。(Comparative Example 1) As in Example 1, the UAE M
A gas turbine fuel oil was produced using urban crude oil according to Japanese Patent Application Laid-Open No. 6-207179. According to the same report, a gas turbine fuel oil having a sulfur concentration of 0.05 wt% or less is produced by using a low-sulfur crude oil whose salt concentration is adjusted to 0.5 ppm or less as a raw material by a distillation method. Gas turbine fuel oil is limited to kerosene fractions from light naphtha up to a boiling point of 230 ° C. No alkali metal, alkaline earth metal, V and lead are detected, the sulfur concentration is about 490 ppm, and the viscosity is 1
Although the quality was as high as 0.1 cSt at 00 ° C., the yield of the gas turbine fuel oil relative to the feed oil was a low recovery of 39%.
【0040】精製プラントでの所内消費率を3%とする
以外、実施例1と同じ条件下においてシミュレーション
を実施した。精製プラントへの原油供給を熱量換算で1
00単位とし、最終的な電力回収量を算定したところ、
熱量換算において41.1単位の電力エネルギー回収が
できるのみで、本発明に比べエネルギー有効利用の観点
から著しく劣後していることが判明した。A simulation was performed under the same conditions as in Example 1 except that the in-house consumption rate in the refinery plant was 3%. The crude oil supply to the refinery plant is 1 calorie equivalent
When the final power recovery amount was calculated as 00 units,
Only 41.1 units of power energy could be recovered in terms of calorific value, which proved to be significantly inferior to the present invention from the viewpoint of effective energy utilization.
【0041】(実施例2)図3に示す本発明でのプロセ
スによりアラビアンライト原油(硫黄濃度:1.77w
t%)によりタービン油製造を試みた。100重量単位
の原油は脱塩工程を経た後、常圧蒸留工程で沸点が36
0℃よりも低い軽質油(60重量単位)と沸点がそれよ
り高い重質油(40重量単位)とに分離し、第1の水素
化処理工程における水素ガスの圧力を45kg/cm
2、LHSV2hr-1に設定し、硫黄濃度50ppmの
深度脱硫精製油を得た。また第1の分離工程である減圧
蒸留工程では沸点(常圧時の沸点)が560℃よりも低
い減圧軽油(23重量単位)と沸点がそれよりも高い重
質油(17重量単位)とに分離した。この減圧軽油を第
2の水素化精製装置において、水素ガスの圧力を75k
g/cm2、LHSV0.8hr-1に設定し、硫黄濃度
300ppmの脱硫精製油を得た。さらにこの重質油を
第2の分離工程であるSDAにかけ硫黄濃度1000p
pm脱れき油(3重量単位)を回収した。この脱れき
油、第2の水素化処理得られた軽質油と第1の水素化処
理で得られたガスタービン燃料油と混合した。ガスター
ビン油全体として、回収率は85重量単位となり、アル
カリ金属0.7ppm、Ca0.8ppm、バナジウム
0.5ppm、鉛は検出されず、硫黄濃度において49
0ppm、粘度は100℃で0.8cStのガスタービ
ン油製造が可能となった。Example 2 Arabian light crude oil (sulfur concentration: 1.77 watts) was obtained by the process of the present invention shown in FIG.
(%), turbine oil production was attempted. 100 weight units of crude oil undergoes a desalting process and then has a boiling point of 36 in an atmospheric distillation process.
Light oil (60 weight units) lower than 0 ° C. and heavy oil (40 weight units) having a higher boiling point are separated, and the pressure of hydrogen gas in the first hydrotreating step is reduced to 45 kg / cm.
2. A LHSV of 2 hr-1 was obtained to obtain a deep desulfurized refined oil having a sulfur concentration of 50 ppm. In the first distillation step, ie, a vacuum distillation step, a vacuum gas oil (23 weight units) having a boiling point (boiling point at normal pressure) lower than 560 ° C. and a heavy oil (17 weight units) having a higher boiling point than that are obtained. separated. In a second hydrorefining unit, the pressure of the reduced pressure gas oil is reduced to 75 k
g / cm 2, LHSV 0.8 hr −1, and a desulfurized refined oil having a sulfur concentration of 300 ppm was obtained. Further, this heavy oil is subjected to SDA as a second separation step, and the sulfur concentration is 1000 p.
The pm degreasing oil (3 weight units) was recovered. The deoiled oil, the light oil obtained in the second hydrotreating, and the gas turbine fuel oil obtained in the first hydrotreating were mixed. The recovery rate of the gas turbine oil as a whole was 85 weight units, and 0.7 ppm of alkali metal, 0.8 ppm of Ca, 0.5 ppm of vanadium, and no lead were detected.
It became possible to produce a gas turbine oil having 0 ppm and a viscosity of 0.8 cSt at 100 ° C.
【0042】原油からのエネルギーは全て電力(ガスタ
ービン及びボイラー発電)に転換するとしてシミュレー
ションを実施した。尚精製プラントでの所内消費率は5
%とし、コンバインドサイクルガスタービン発電効率4
9%、ボイラー発電効率38%に設定した。以上の条件
下において精製プラントへの原油供給を熱量換算で10
0単位とし、最終的な電力回収量を算定したところ、熱
量換算において45.1単位のエネルギー回収が可能と
なった。The simulation was performed assuming that all the energy from crude oil was converted to electric power (gas turbine and boiler power generation). The on-site consumption rate at the refinery plant is 5
%, Combined cycle gas turbine power generation efficiency 4
9% and boiler power generation efficiency were set to 38%. Under the above conditions, supply of crude oil to the refinery plant
When the final power recovery amount was calculated using 0 units, it was possible to recover 45.1 units of energy in terms of calorific value.
【0043】(比較例2)実施例1と同様に原油として
アラビアンライト油を用い、特開平6−207179に
よりガスタービン燃料油を製造した。本報からのガスタ
ービン燃料油は、沸点領域245℃までの軽質ナフサか
ら灯油留分に限られ、アルカリ金属、アルカリ土類金
属、V及び鉛は検出されず、硫黄濃度はおよそ470p
pm、粘度は100℃で0.3cStと高品質であった
が、原料油に対するガスタービン燃料油の収率は24%
と極めて低い回収率であった。Comparative Example 2 A gas turbine fuel oil was produced in the same manner as in Example 1 by using Arabian light oil as a crude oil according to JP-A-6-207179. Gas turbine fuel oil from this report is limited to kerosene fractions from light naphtha with boiling point range up to 245 ° C, alkali metal, alkaline earth metal, V and lead are not detected and sulfur concentration is about 470p
pm and a viscosity of 0.3 cSt at 100 ° C., but the gas turbine fuel oil yield based on the feed oil was 24%
And an extremely low recovery rate.
【0044】精製プラントでの所内消費率を3%とする
以外、実施例1と同じ条件下においてシミュレーション
を実施した。精製プラントへの原油供給を熱量換算で1
00単位とし、最終的な電力回収量を算定したところ、
熱量換算において39.5単位の電力エネルギー回収が
できるのみで本発明に比べエネルギー有効利用の観点か
ら著しく劣後していることが判明した。The simulation was performed under the same conditions as in Example 1 except that the in-house consumption rate in the refinery plant was 3%. The crude oil supply to the refinery plant is 1 calorie equivalent
When the final power recovery amount was calculated as 00 units,
It was found that only 39.5 units of power energy could be recovered in calorie conversion, which was significantly inferior to the present invention from the viewpoint of effective energy utilization.
【0045】[0045]
【発明の効果】以上のように本発明によれば、原油を常
圧蒸留し、その軽質油に対して水素化処理を行って精製
油を得ると共に、常圧残渣油に対して分離処理を行っ
て、得られた軽質油の少なくとも一部と前記精製油とを
混合してガスタービン燃料油としている。また常圧残渣
油に対して第1の分離工程を行って得た軽質油を水素化
処理すると共に、水素化処理で得た精製油と、常圧軽油
を水素化処理して得た精製油と、第1の分離工程で得た
重質油から更に分離して得た軽質油の少なくとも一部と
を混合してガスタービン燃料油を得ているため、品質の
高いガスタービン燃料油を高い収率で得ることができ
る。As described above, according to the present invention, crude oil is subjected to normal pressure distillation, the light oil is subjected to hydrogenation treatment to obtain a refined oil, and the normal pressure residue oil is subjected to separation treatment. The gas turbine fuel oil is obtained by mixing at least a part of the obtained light oil and the refined oil. Further, the light oil obtained by performing the first separation step on the atmospheric residual oil is subjected to hydrogenation treatment, and the refined oil obtained by the hydrogenation treatment and the refined oil obtained by hydrotreating the atmospheric pressure gas oil And at least a portion of light oil obtained by further separating from the heavy oil obtained in the first separation step to obtain gas turbine fuel oil. It can be obtained in yield.
【図1】本発明方法を実施するためのシステムの一例を
示す説明図である。FIG. 1 is an explanatory diagram showing an example of a system for implementing a method of the present invention.
【図2】上記システムにおいて常圧蒸留塔からの軽質油
の取り出し方法の他の例を示す説明図である。FIG. 2 is an explanatory view showing another example of a method for removing light oil from an atmospheric distillation column in the above system.
【図3】水素化処理装置の一例を示す説明図である。FIG. 3 is an explanatory diagram illustrating an example of a hydrotreating apparatus.
【図4】水素プラントの要部の一例を示す説明図であ
る。FIG. 4 is an explanatory diagram showing an example of a main part of a hydrogen plant.
【図5】本発明方法を実施するためのシステムの他の例
を示す説明図である。FIG. 5 is an explanatory diagram showing another example of a system for implementing the method of the present invention.
【図6】本発明方法を実施するためのシステムの更に他
の一例を示す説明図である。FIG. 6 is an explanatory diagram showing still another example of a system for implementing the method of the present invention.
【図7】本発明方法を実施するためのシステムの更にま
た他の例を示す説明図である。FIG. 7 is an explanatory diagram showing still another example of a system for implementing the method of the present invention.
【図8】本発明で得られるガスタ−ビン燃料油の使用方
法の一例を示す説明図である。FIG. 8 is an explanatory diagram showing an example of a method for using gas turbine fuel oil obtained in the present invention.
1 原料油 11 脱塩処理部 2 常圧蒸留塔 21 軽質油 22 常圧残渣油 3 第1の水素化処理装置 4 水素プラント 5 減圧蒸留塔 6 溶剤脱れき装置 7 第2の水素化処理装置 60 第3の水素化処理装置 201 ガスタ−ビン 203 排熱回収ボイラ− 204 スチ−ムタ−ビン DESCRIPTION OF SYMBOLS 1 Raw material oil 11 Desalination processing part 2 Normal pressure distillation column 21 Light oil 22 Normal pressure residue oil 3 First hydrotreating unit 4 Hydrogen plant 5 Vacuum distillation column 6 Solvent dewatering device 7 Second hydrotreating device 60 Third Hydrotreating Device 201 Gas Turbine 203 Exhaust Heat Recovery Boiler 204 Steam Turbine
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C10L 1/04 C10L 1/04 (72)発明者 増子 芳範 神奈川県横浜市西区みなとみらい2−3− 1 日揮株式会社内 (72)発明者 徳田 慎一 神奈川県横浜市西区みなとみらい2−3− 1 日揮株式会社内 Fターム(参考) 4H029 AA11 AB01 AB05 AC04 DA01 DA02 DA05 DA09 ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) C10L 1/04 C10L 1/04 (72) Inventor Yoshinori Masuko 2-3-1 Minato Mirai, Nishi-ku, Yokohama-shi, Kanagawa Nikko (72) Inventor Shinichi Tokuda 2-3-1 Minatomirai, Nishi-ku, Yokohama-shi, Kanagawa Japan JGC Corporation F-term (reference) 4H029 AA11 AB01 AB05 AC04 DA01 DA02 DA05 DA09
Claims (8)
と常圧残渣油とに分離する常圧蒸留工程と、 この常圧蒸留工程で得られた軽質油を一括して触媒の存
在下で加圧された水素と接触させて脱不純物処理を行い
硫黄濃度が150ppm以下の精製油を得る第1の水素
化処理工程と、前記常圧残渣油を軽質油と重質油とに分
離する、減圧蒸留工程、溶剤脱れき工程、熱分解工程及
び水蒸気蒸留工程から選ばれる第1の分離工程と、 前記第1の分離工程にて得られた軽質油を水素化処理す
ることなく少なくともその一部と前記精製油とを混合し
てガスタ−ビン燃料油を得る混合工程と、を含み、 この混合工程で得られたガスタービン燃料油は、粘度が
100℃で4cSt以下、アルカリ金属が1ppm 以下、
鉛が1ppm 以下、Vが0.5ppm以下、Caが2pp
m以下、硫黄が500ppm 以下であることを特徴とする
ガスタ−ビン燃料油の製造方法。1. An atmospheric distillation step in which a crude oil as a feed oil is subjected to atmospheric distillation to separate a light oil and an atmospheric residual oil, and the light oil obtained in the atmospheric distillation step is collectively used as a catalyst. A first hydrotreating step of contacting with pressurized hydrogen in the presence to perform a de-impurity treatment to obtain a refined oil having a sulfur concentration of 150 ppm or less, and converting the normal pressure residue oil into light oil and heavy oil Separating, a first separation step selected from a reduced pressure distillation step, a solvent removal step, a thermal decomposition step and a steam distillation step, and at least without subjecting the light oil obtained in the first separation step to a hydrogenation treatment. A mixing step of mixing a part thereof with the refined oil to obtain a gas turbine fuel oil. The gas turbine fuel oil obtained in the mixing step has a viscosity of 4 cSt or less at 100 ° C. and an alkali metal. 1 ppm or less,
Lead is 1 ppm or less, V is 0.5 ppm or less, Ca is 2 pp
m and a sulfur content of 500 ppm or less.
油と常圧残渣油とに分離する常圧蒸留工程と、 この常圧蒸留工程で得られた軽質油を一括して触媒の存
在下で加圧された水素と接触させて脱不純物処理を行い
硫黄濃度が150ppm以下の精製油を得る第1の水素
化処理工程と、 前記常圧残渣油を軽質油と重質油とに分離する、減圧蒸
留工程、溶剤脱れき工程、熱分解工程及び水蒸気蒸留工
程から選ばれる第1の分離工程と、 前記第1の分離工程にて得られた重質油を更に軽質油と
重質油とに分離する、溶剤脱れき工程及び熱分解工程か
ら選ばれる第2の分離工程と、 前記第2の分離工程にて得られた軽質油を水素化処理す
ることなく少なくともその一部と前記第1の分離工程に
て得られた水素化処理をしない軽質油と前記精製油とを
混合してガスタ−ビン燃料油を得る混合工程と、を含
み、 この混合工程で得られたガスタービン燃料油は、粘度が
100℃で4cSt以下、アルカリ金属が1ppm 以下、
鉛が1ppm 以下、Vが0.5ppm以下、Caが2pp
m以下、硫黄が500ppm 以下であることを特徴とする
ガスタ−ビン燃料油の製造方法。2. An atmospheric distillation step in which crude oil as a feed oil is subjected to atmospheric distillation to separate it into a light oil and an atmospheric residue, and the light oil obtained in the atmospheric distillation step is collectively used as a catalyst. A first hydrotreating step of contacting with pressurized hydrogen in the presence to perform a de-impurity treatment to obtain a refined oil having a sulfur concentration of 150 ppm or less, and converting the normal-pressure residue oil into a light oil and a heavy oil Separating, a first separation step selected from a vacuum distillation step, a solvent removal step, a thermal decomposition step and a steam distillation step; and the heavy oil obtained in the first separation step is further combined with a light oil and a heavy oil Separating into oil, a second separation step selected from a solvent removal step and a thermal decomposition step, and at least a part of the light oil obtained in the second separation step without hydrotreating and The light oil not subjected to hydrotreating obtained in the first separation step and the refined oil are combined with each other. Combined Antofagasta and - comprises a mixing step of obtaining a bottle fuel oil, the gas turbine fuel oil obtained in this mixing step, viscosity of 4cSt less at 100 ° C., the alkali metal is 1ppm or less,
Lead is 1 ppm or less, V is 0.5 ppm or less, Ca is 2 pp
m and a sulfur content of 500 ppm or less.
%以下であり、原料油に対するガスタ−ビン燃料油の収
率が60%を越えることを特徴とする請求項1または2
記載のガスタ−ビン燃料油の製造方法。3. The method according to claim 1, wherein the sulfur content in the feedstock is 1.5% by weight or less, and the yield of gas turbine fuel oil based on the feedstock exceeds 60%.
A method for producing the gas turbine fuel oil according to the above.
と常圧残渣油とに分離する常圧蒸留工程と、 この常圧蒸留工程で得られた軽質油を一括して触媒の存
在下で加圧された水素と接触させて脱不純物処理を行い
硫黄濃度が150ppm以下の精製油を得る第1の水素
化処理工程と、前記常圧残渣油を軽質油と重質油とに分
離する、減圧蒸留工程、溶剤脱れき工程、熱分解工程及
び水蒸気蒸留工程から選ばれる第1の分離工程と、 この第1の分離工程にて得られた軽質油を触媒の存在下
で加圧された水素と接触させて脱不純物処理を行い精製
油を得る第2の水素化処理工程と、 前記第1の分離工程にて得られた重質油を更に軽質油と
重質油とに分離する、溶剤脱れき工程及び熱分解工程か
ら選ばれる第2の分離工程と、 前記第2の分離工程にて得られた軽質油を水素化処理す
ることなく少なくともその一部と前記第1の水素化処理
工程にて得られた精製油と前記第2の水素化処理工程で
得られた精製油とを混合してガスタ−ビン燃料油を得る
混合工程と、を含み、 この混合工程で得られたガスタービン燃料油は、粘度が
100℃で4cSt以下、アルカリ金属が1ppm 以下、
鉛が1ppm 以下、Vが0.5ppm以下、Caが2pp
m以下、硫黄が500ppm 以下であることを特徴とする
ガスタ−ビン燃料油の製造方法。4. An atmospheric distillation step in which a crude oil as a feed oil is subjected to atmospheric distillation to separate it into a light oil and an atmospheric residue, and the light oil obtained in the atmospheric distillation step is collectively used as a catalyst. A first hydrotreating step of contacting with pressurized hydrogen in the presence to perform a de-impurity treatment to obtain a refined oil having a sulfur concentration of 150 ppm or less, and converting the normal pressure residue oil into light oil and heavy oil Separating, a first separation step selected from a vacuum distillation step, a solvent removal step, a thermal decomposition step and a steam distillation step; and pressurizing the light oil obtained in the first separation step in the presence of a catalyst. A second hydrotreating step of obtaining a refined oil by performing a de-impurity treatment by bringing the heavy oil into contact with the hydrogen, and further separating the heavy oil obtained in the first separation step into a light oil and a heavy oil A second separation step selected from a solvent stripping step and a thermal decomposition step, and the second separation step The light oil obtained by the above-mentioned method is subjected to at least a part thereof without hydrotreating, the refined oil obtained in the first hydrotreating step and the refined oil obtained in the second hydrotreating step. A mixing step of mixing to obtain a gas turbine fuel oil. The gas turbine fuel oil obtained in this mixing step has a viscosity of 4 cSt or less at 100 ° C., an alkali metal of 1 ppm or less,
Lead is 1 ppm or less, V is 0.5 ppm or less, Ca is 2 pp
m and a sulfur content of 500 ppm or less.
処理工程は共通の工程であることを特徴とする請求項4
記載のガスタ−ビン燃料油の製造方法。5. The process according to claim 4, wherein the first hydrotreating step and the second hydrotreating step are common steps.
A method for producing the gas turbine fuel oil according to the above.
量%以下であり、原料油に対するガスタ−ビン燃料油の
収率が70%以上であることを特徴とする請求項4また
は5記載のガスタ−ビン燃料油の製造方法。6. The feedstock according to claim 4, wherein the sulfur content in the feedstock is 3.0% by weight or less, and the yield of gas turbine fuel oil to the feedstock is 70% or more. For producing gas turbine fuel oil.
造方法により製造されたガスタ−ビン燃料油。7. A gas turbine fuel oil produced by the production method according to claim 1.
油を燃料としてガスタ−ビンを駆動させて発電を行う工
程と、 前記ガスタ−ビンから排出される高温排ガスを排熱回収
ボイラ−の熱源とし、この排熱回収ボイラ−にて発生し
た蒸気により蒸気タ−ビンを駆動して発電を行う工程
と、を含むことを特徴とする発電方法。8. A step of generating electricity by driving the gas turbine using the gas turbine fuel oil produced in claim 7 as a fuel, and providing a high-temperature exhaust gas discharged from the gas turbine to an exhaust heat recovery boiler. Generating a power by driving a steam turbine with steam generated by the exhaust heat recovery boiler as a heat source.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11095203A JP2000282060A (en) | 1999-04-01 | 1999-04-01 | Gas turbine fuel oil, its production and power generation method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11095203A JP2000282060A (en) | 1999-04-01 | 1999-04-01 | Gas turbine fuel oil, its production and power generation method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2000282060A true JP2000282060A (en) | 2000-10-10 |
Family
ID=14131202
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11095203A Withdrawn JP2000282060A (en) | 1999-04-01 | 1999-04-01 | Gas turbine fuel oil, its production and power generation method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2000282060A (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002034865A1 (en) * | 2000-10-24 | 2002-05-02 | Jgc Corpopation | Refined oil and process for producing the same |
| WO2002044307A1 (en) * | 2000-11-30 | 2002-06-06 | Jgc Corporation | Method of refining petroleum |
| CN107001952A (en) * | 2014-11-21 | 2017-08-01 | 鲁姆斯科技公司 | The method of the decompression residuum of upgrading part conversion |
| CN109803754A (en) * | 2016-10-18 | 2019-05-24 | 马威特尔有限责任公司 | The turbine fuel of polishing |
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1999
- 1999-04-01 JP JP11095203A patent/JP2000282060A/en not_active Withdrawn
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|---|---|---|---|---|
| WO2002034865A1 (en) * | 2000-10-24 | 2002-05-02 | Jgc Corpopation | Refined oil and process for producing the same |
| US7384537B2 (en) | 2000-10-24 | 2008-06-10 | Jgc Corporation | Refined oil and process for producing the same |
| WO2002044307A1 (en) * | 2000-11-30 | 2002-06-06 | Jgc Corporation | Method of refining petroleum |
| CN100387690C (en) * | 2000-11-30 | 2008-05-14 | 日挥株式会社 | oil refining method |
| CN107001952A (en) * | 2014-11-21 | 2017-08-01 | 鲁姆斯科技公司 | The method of the decompression residuum of upgrading part conversion |
| CN107001952B (en) * | 2014-11-21 | 2019-01-11 | 鲁姆斯科技公司 | The method of the decompression residuum of upgrading part conversion |
| CN109803754A (en) * | 2016-10-18 | 2019-05-24 | 马威特尔有限责任公司 | The turbine fuel of polishing |
| CN109803754B (en) * | 2016-10-18 | 2021-11-02 | 马威特尔有限责任公司 | Polished Turbine Fuel |
| JP2020114922A (en) * | 2020-04-01 | 2020-07-30 | マウェタール エルエルシー | fuel |
| JP2021165395A (en) * | 2020-04-01 | 2021-10-14 | マウェタール エルエルシー | Fuels |
| JP2022010095A (en) * | 2020-04-01 | 2022-01-14 | マウェタール エルエルシー | Fuels |
| JP7002590B2 (en) | 2020-04-01 | 2022-01-20 | マウェタール エルエルシー | fuel |
| CN114674780A (en) * | 2022-03-16 | 2022-06-28 | 中国石油化工股份有限公司 | Blending method of light crude oil |
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