JPH0115558B2 - - Google Patents
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- Publication number
- JPH0115558B2 JPH0115558B2 JP21652684A JP21652684A JPH0115558B2 JP H0115558 B2 JPH0115558 B2 JP H0115558B2 JP 21652684 A JP21652684 A JP 21652684A JP 21652684 A JP21652684 A JP 21652684A JP H0115558 B2 JPH0115558 B2 JP H0115558B2
- Authority
- JP
- Japan
- Prior art keywords
- oil
- heavy oil
- heavy
- mixture
- temperature
- 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.)
- Expired
Links
- 239000000295 fuel oil Substances 0.000 claims description 75
- 238000000034 method Methods 0.000 claims description 41
- 239000000203 mixture Substances 0.000 claims description 35
- 239000003921 oil Substances 0.000 claims description 35
- 238000004519 manufacturing process Methods 0.000 claims description 25
- 239000000126 substance Substances 0.000 claims description 23
- 239000002994 raw material Substances 0.000 claims description 20
- 238000001816 cooling Methods 0.000 claims description 15
- 239000010724 circulating oil Substances 0.000 claims description 13
- 239000003208 petroleum Substances 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 5
- 239000011280 coal tar Substances 0.000 claims description 4
- 238000004517 catalytic hydrocracking Methods 0.000 claims description 3
- 238000005336 cracking Methods 0.000 claims description 3
- 238000004821 distillation Methods 0.000 claims description 3
- 238000004227 thermal cracking Methods 0.000 claims description 3
- 238000010924 continuous production Methods 0.000 claims description 2
- 239000007788 liquid Substances 0.000 description 25
- 238000002156 mixing Methods 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 238000000605 extraction Methods 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 238000010586 diagram Methods 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 238000004523 catalytic cracking Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000004220 aggregation Methods 0.000 description 3
- 230000002776 aggregation Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000004939 coking Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000002198 insoluble material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 238000005120 petroleum cracking Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
Landscapes
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
〔発明の技術分野〕
本発明は、ガソリン製造用原料油の製造法に関
し、さらに詳しくは、脱金属、脱アスフアルテン
を効果的に行なうことにより、ガソリンの製造に
適した良質の原料油を連続的に製造するための方
法に関する。
〔発明の背景〕
近年、石油資源の有効利用の観点から、石油系
重質残油の改質法に関する研究が種々進められて
いる。
一般に、重質油からガソリン製造用の原料油を
調製する場合、重質油中のアスフアルテンや金属
成分などの不純物をいかに効果的に除去するか、
が重要な問題となる。原料油中に存在するアスフ
アルテンや重金属類は、その後の接触分解等の精
製工程において有害な成分となり、特にNi,Fe,
V等の金属は接触分解触媒のコーキングを促進し
たり触媒活性を低下させて、ガソリンの液収率を
減少させる要因となる。
重質油の脱金属、脱アスフアルテンの主な方法
としては、従来、(イ)プロパン等の低沸点パラフイ
ン系炭化水素またはベンゼン、トルエンなどの有
機溶剤を重質油と接触させてアスフアルテン類を
分離除去する溶剤脱歴法(たとえば、特開昭59−
27985号公報、同57−31989号公報、同53−54205
号公報等、同59−41389号公報等)、(ロ)特定の固体
触媒を用いる方法(たとえば、特開昭52−117905
号公報、同54−113602号公報等)、(ハ)コールター
ルと石油系重質油のように、履歴および芳香性等
の性状の異なる二種以上の重質油を混合し、加
熱、冷却工程を経ることにより重質油中の有害な
不純物である不溶性物質を沈積させて除去するバ
ツチ方法(たとえば、特公昭49−26481号公報、
特開昭49−11603号公報等)、などが知られてい
る。
しかしながら、上記(イ)の溶剤を使用する方法に
あつては、溶剤の分離工程や回収工程が必要とな
るため製造工程が複雑化するとともに、溶剤の選
定、脱歴条件の設定など、製造条件の最適な選択
が必ずしも容易ではなく、さらに、製造コストが
増大するという欠点がある。
また、上記(ロ)の触媒を用いる方法においても、
同様に、触媒の選定、触媒活性能の維持・再生、
さらには失活した触媒の除去などの複雑な工程が
必要になるとともに製造コストが増大するなどの
問題があり、技術的、経済的に不利がある。
さらに、上記(ハ)の方法においては、不溶性物質
の生成およびその除去は、静置冷却、ならびに静
置沈降分離あるいは遠心分離等により行われるも
のであり、いずれもバツチ操作が要求される。し
かし、バツチ操作は、周知のように生産性が悪
く、またバツチ毎に品質が変化するという欠点が
ある。
〔発明の概要〕
本発明は、上記従来技術が有する欠点に鑑みて
なされたものであり、重質油からの脱金属、脱ア
スフアルテンを効果的に行うことにより、ガソリ
ン製造用原料油を効率的かつ連続的に調製するた
めの方法を提供することを目的とする。
本発明者らは、二種以上の重質油の混合によつ
て生成する不溶性物質中に、接触分解工程等にお
ける障害となる金属成分の大部分が濃縮されると
いう事実に着目するとともに、この不溶性物質を
効率的に分離し除去するための方法を種々試みた
結果、高温に調製した重質油混合物の流れと、一
部抜出して循環させた製品原料油とを接触ないし
衝突させて高温重質油混合物を急冷することによ
り不溶性物質の生成ならびに凝集が促進させて脱
金属、脱アスフアルテンが連続操作により効果的
に達成されることを見出した。
本発明は上記知見に基いてなされたものであ
る。すなわち、本発明のガソリン製造用原料油の
連続製造法は、少なくとも二種の重質油からなる
高温の重質油混合物を調製し、さらにこの混合物
を冷却することにより重質油混合物中に不溶性物
質を生成させ、この不溶性物質を重質油混合物か
ら除去することによりガソリン製造用原料油を連
続的に製造するに際し、製造されたガソリン製造
用原料油の一部を抜出して前記冷却工程に循環さ
せ、この循環油の流れと前記高温の重質油混合物
の流れを接触させることにより重質油混合物の冷
却を行うことを特徴とするものである。
第1図は、本発明の方法の概要を示す工程図で
ある。
第1図に示すように、本発明方法においては、
まず、石油系の常圧ないし減圧直留残渣油、コー
ルタール、石油系のナフサ分解残渣油、熱分解残
渣油または水素化分解残渣油等から選ばれる少な
くとも二種の重質油からなる高温200〜390℃の重
質油混合物を調製する。この高温重質油混合物の
調製は、成分となる重質油を各々あらかじめ加熱
した後これらを合流させる方法(ラインブレンデ
イング)により行うことが好ましいが、成分とな
る重質油を混合したのち、または混合しながら加
熱することによつても行い得る。
次いで、高温重質油混合物を100℃以下の温度
に冷却して重質油混合物中に不溶性物質を生成さ
せる。本発明の方法においては、この冷却工程
を、既に製造されたガソリン製造用原料油の一部
を抜出して循環油とし、この循環油の流れと高温
重質油混合物の流れとを接触させることにより行
う。循環油は、高温重質油混合物に接触させる前
にあらかじめ50〜80℃に冷却しておく必要がある
が、循環経路を移動する間に循環油が自然放冷に
よつて上記温度範囲となる場合にあつては、必ず
しも強制的に冷却する必要はない。
なお、循環油の温度が約50℃以下になると、一
般に、流動性が低下するので好ましくない。
上記冷却工程は、高温重質油混合物の噴流と循
環油の噴流とを向流接触ないし向流衝突させるこ
とにより行なうことが好ましい。このようにし
て、循環油と重質油混合物とが衝突する運動によ
り高温の重質油混合物が急冷させて不溶性物質の
生成に必要な温度条件が満足されるとともに、析
出した不溶分の衝突によつて不溶分の凝集が促進
される。
一方、このようにして析出、凝集した不溶性物
質を逐次分離除去し回収して、連続的なガソリン
製造用原料油の調製が達成される。
〔発明の具体的説明〕
以下、本発明の方法をその好ましい具体例に基
いてさらに詳細に説明する。
第2図は、本発明の方法を実施するために用い
る装置の要部配置図であり、第3図は第2図に示
す要部を含む全体配置図である。
第2図および第3図に示すように、本発明の方
法を実施するための装置は、ほぼ垂直に配列した
ほぼ同径の円筒状の上槽1と下槽2とを、たとえ
ばこれらの槽の径の1/2〜1/10好ましくは1/5〜1/
6の径を有する比較的細い管径の筒管3により結
合してなる。下槽2にはその側壁を貫通して単一
の重質油導入管4が導入され、その下流端は下槽
2内で前記筒管3に向けて上方に開口している。
また、導入管4の上流は、下槽2の比較的近くに
おいて、それぞれの原料重質油の導入管4aおよ
び4bに分岐しており、これら導入管4aおよび
4bは、それぞれ加熱器5aまたは5b、ポンプ
6aまたは6bを経由して、原料重質油タンク7
aまたは7bに結合している。また下槽2の底部
には重液の抜出配管8が結合され、この抜出配管
8は、ポンプ9を経て重液タンク10に結合して
いる。
一方、上槽1の上部には軽液抜出管11が結合
されており、この抜出管11は、受槽12、ポン
プ13を経由して製品油タンク14に結合され
る。また抜出管11のポンプ13下流には、循環
配管15が分岐結合されており、この循環配管1
5は上槽1内に延長し、上槽1内で筒管3に向け
て下方に開口している。この循環配管15の途中
には、冷却器16が配設されている。また上槽1
内には、その一方の側壁から対向側壁に向けて、
複数のほぼ水平な棚板17が延長しており、その
下方のいくつかは、槽1の中心部を越えて対向側
壁側へ延長している。
また、槽1および槽2の底部周囲には、加熱器
20a,20bが配設されている。
次に、上記装置を用いて、ガソリン製造用の原
料油を調製する代表的な態様について説明する。
以下の説明において「部」および「%」は、特に
断わらない限り重量基準とする。
まずタンク7aからは、比較的芳香性の低い重
質油Aを、またタンク7bからは比較的芳香性の
高い重質油Bを、それぞれポンプ6aまたは6b
を経て、加熱器5aまたは5bにより、200〜390
℃に加熱したのち、下槽2の直前において合流さ
せ2液の混合を行ない、導入管4を通じて下槽2
内の筒管3の直下に流出ないし噴出させる。
重質油Aとしては、たとえば石油系の常圧ない
し減圧直留残渣油等が、また重質油Bとしては、
コールタール、石油系のナフサ分解残渣油、熱分
解残渣油あるいは水素化分解残渣油等が用いられ
る。重質油Bは不溶性物質の除去効率ならびに製
品原料油の性状を考慮して、混合油100部に対し
て30〜70部で使用することが好ましい。
導入された高温重質油混合物は、主として筒管
3を通つて上昇し、かつ循環配管15、冷却器1
6を介して流出する循環軽液(50〜90)℃との接
触ないし衝突により、好ましくは100℃以下に冷
却され、これら一連の混合および冷却により生成
した不溶性物質は、凝集および沈降が促進され、
筒管3を通つて重質油混合物と接触しつつ流下
し、下槽2の底部に沈積する。主として沈積され
た不溶性物質からなる重液は、加熱器20bによ
り加熱されて流動性を保持した状態で底部配管8
から抜き出され、ポンプ9を経て重液タンク10
に保留される。
一方、上槽1において不溶性物質を除いた軽液
は、更に棚板17間を通つて上昇しつつ更に不溶
性物質を分離し、上槽1の上部より配管11を経
て抜き出され、受槽12、ポンプ13を経て製品
油タンク14に貯留される。またポンプ13を出
た軽液の一部は、配管15を経由して、上槽1へ
と循環し、上槽1内の棚板17の下へと流出させ
られる。
上記において、本発明方法の好ましい一例なら
びにその運転態様を具体的装置に基いて説明し
た。しかしながら本発明の範囲内で、上記例の方
法を各種変形することが可能であることは当業者
には容易に理解できよう。たとえば、原料重質油
としては、2種に限らず、3種あるいはそれ以上
のものを用いることができる。また、原料重質油
の導入管4は、下槽2内に延長させ、筒管3の直
下に開口させることが好ましいが、これに限らず
下槽2の側壁に開口させてもそれなりの効果が得
られる。導入管4は、また単一管に限らず、原料
重質油ごとに複数の導入管を下槽2に結合ないし
下槽2内に延長させることもできる。更に、上槽
1内の棚板17は、軽液と不溶性物質の分離を促
進する効果があるが、棚板17上への不溶性物質
の沈積を防止するために、斜め下方に傾斜させる
ことも好ましい。上槽1と下槽2の容積は、上記
例において、ほぼ同容積であるが混合分離を考慮
して、適宜その比を変化させることもできる。
上述したような方法によれば、原料油の混合を
配管中でしかも高温で行ない(ラインブレンド)、
さらに冷却ならびに沈積は比較的大きな容量の槽
中で行なえるため、生成する不溶性物質による配
管の閉塞の問題もない。さらに、製品軽液の一部
の循環等により、混合および分離に必要な温度差
が与えられ、これら温度の設定、制御も容易とな
る。
〔発明の実施例〕
以下に、本質的に第2図および第3図に示す本
発明の方法で用いる装置例の実際の運転例を示
す。以下の例は、比較的小規模の実施例である
が、本発明の方法の有効性については充分に理解
できるものと考えられる。
下記第1表に示す性状を有する石油系重質油
A、エチレンタール石油分解系重質油B、石炭系
重質油Cを原料重質油としてガソリン製造用原料
油の製造を行つた。
実施例 1
重質油Aを140g/分、重質油Bを60g/分の
割合でフイードポンプ6a,6bより送給し、加
熱器5a,5bにてそれぞれ200℃に加熱したの
ち、配管4a,4bから下槽2(径約250mm、40
)の直前で配管4に合流させ、下槽2内の筒管
3(径約50mm、長さ200mm)の下端の直下100mmの
位置から流出させた。重質油Aと重質油Bの配合
比は、A:B=70:30であつた。
一方、図示のような棚板17(計5枚)を備え
る上槽1(径約300mm)の棚板下には配管15、
冷却器16を通つて温度約80℃の軽液を1/分
の速度で循環させ重質油混合物の噴流と接触させ
て重質油混合物を100℃以下の温度へ急冷させた。
上槽1から抜出された軽液を、貯槽14の位置
で166g/分(収率83%)の割合で回収し、一方
下槽2の底部配管8からは約200℃に加熱して流
動性を与えた主として不溶性物質からなる重液を
回収した。
回収した軽液ならびに重液中の金属含有量およ
び性状は第1表に示すとおりであつた。
実施例 2
重質油Aならびに重質油Cを用いて、上記実施
例1と同様の方法、条件で重質油混合物から軽液
および重液を回収し、金属含有量、性状を分析し
た。分析結果は第1表に示すとおりであつた。
比較例
重質油Aを、常法に従つて、溶剤としてノルマ
ンヘプタンを用いた溶剤脱歴法によつて脱歴し、
得られた軽液の金属含有量ならびに性状を分析し
た。分析結果は、第1表に示す通りであつた。
上記分析結果から明らかなように、本発明の方
法に係る実施例1および実施例2で得られた軽液
は、比較例と比べて脱金属効果がすぐれ、特に、
接触分解工程においてコーキングを促進したり、
触媒活性を低下させる要因となるNi成分が極め
て効果的に除去されていることがわかる。
[Technical Field of the Invention] The present invention relates to a method for producing raw material oil for gasoline production, and more specifically, the present invention relates to a method for producing raw material oil for gasoline production. Relating to a method for manufacturing. [Background of the Invention] In recent years, from the viewpoint of effective utilization of petroleum resources, various studies have been conducted on methods for reforming heavy petroleum residues. In general, when preparing raw material oil for gasoline production from heavy oil, it is difficult to effectively remove impurities such as asphaltene and metal components in the heavy oil.
is an important issue. Asphaltenes and heavy metals present in feedstock oil become harmful components in subsequent refining processes such as catalytic cracking, and especially Ni, Fe,
Metals such as V promote coking of the catalytic cracking catalyst and reduce the catalytic activity, resulting in a decrease in the liquid yield of gasoline. Conventionally, the main methods for demetallizing and removing asphaltenes from heavy oil include (a) separating asphaltenes by contacting the heavy oil with a low-boiling point paraffinic hydrocarbon such as propane or an organic solvent such as benzene or toluene; Solvent deasphalting method to remove (for example, JP-A-59-
Publication No. 27985, Publication No. 57-31989, Publication No. 53-54205
No. 59-41389, etc.), (b) a method using a specific solid catalyst (for example, JP-A No. 52-117905),
No. 54-113602, etc.), (c) Mixing two or more types of heavy oils with different properties such as history and aroma, such as coal tar and petroleum heavy oil, heating and cooling. Batch method in which insoluble substances that are harmful impurities in heavy oil are deposited and removed through a process (for example, Japanese Patent Publication No. 49-26481,
JP-A-49-11603, etc.) are known. However, in the method (a) above that uses a solvent, the manufacturing process becomes complicated because a solvent separation and recovery process is required, and manufacturing conditions such as selecting a solvent and setting deasphalting conditions are required. It is not always easy to select the optimum one, and furthermore, there is a drawback that the manufacturing cost increases. Also, in the method using the catalyst described in (b) above,
Similarly, selection of catalyst, maintenance and regeneration of catalyst activity,
Furthermore, there are problems such as complicated steps such as removal of the deactivated catalyst and increased manufacturing costs, which are disadvantageous from a technical and economic point of view. Furthermore, in the method (c) above, the production of insoluble substances and their removal are performed by stationary cooling, stationary sedimentation separation, centrifugation, etc., and batch operations are required in either case. However, as is well known, batch operations are disadvantageous in that productivity is poor and quality varies from batch to batch. [Summary of the Invention] The present invention has been made in view of the drawbacks of the above-mentioned prior art, and aims to efficiently convert raw material oil for gasoline production by effectively removing metals and asphaltene from heavy oil. and to provide a method for continuous preparation. The present inventors focused on the fact that most of the metal components that become obstacles in the catalytic cracking process etc. are concentrated in the insoluble substances produced by mixing two or more types of heavy oil. As a result of trying various methods to efficiently separate and remove insoluble substances, we have found that the flow of a heavy oil mixture prepared at a high temperature is brought into contact with or collides with the product raw material oil that has been partially extracted and circulated. It has been found that rapid cooling of a quality oil mixture promotes the formation and aggregation of insoluble substances, thereby effectively achieving demetallization and asphaltene removal through continuous operation. The present invention has been made based on the above findings. That is, the continuous production method of raw material oil for gasoline production of the present invention involves preparing a high-temperature heavy oil mixture consisting of at least two kinds of heavy oils, and further cooling this mixture to remove insoluble substances in the heavy oil mixture. When continuously producing raw material for gasoline production by producing substances and removing the insoluble substances from the heavy oil mixture, a part of the produced raw material for gasoline production is extracted and circulated to the cooling step. The heavy oil mixture is cooled by bringing the circulating oil flow into contact with the high temperature heavy oil mixture flow. FIG. 1 is a process chart showing an overview of the method of the present invention. As shown in FIG. 1, in the method of the present invention,
First, a high-temperature 200 ml of heavy oil consisting of at least two types of heavy oil selected from petroleum-based ordinary pressure or vacuum direct distillation residue oil, coal tar, petroleum-based naphtha cracking residue oil, thermal cracking residue oil, hydrocracking residue oil, etc. Prepare a heavy oil mixture at ~390 °C. Preparation of this high-temperature heavy oil mixture is preferably carried out by heating each of the component heavy oils in advance and then combining them (line blending); however, after mixing the component heavy oils, Alternatively, it may be carried out by heating while mixing. The hot heavy oil mixture is then cooled to a temperature below 100° C. to form insoluble materials in the heavy oil mixture. In the method of the present invention, this cooling step is carried out by extracting a part of the already produced raw material oil for gasoline production and using it as circulating oil, and bringing the flow of this circulating oil into contact with the flow of the high-temperature heavy oil mixture. conduct. The circulating oil needs to be cooled to 50 to 80°C before it comes into contact with the high-temperature heavy oil mixture, but the circulating oil naturally cools down to the above temperature range while moving through the circulation path. In some cases, forced cooling is not necessarily necessary. It should be noted that if the temperature of the circulating oil is about 50° C. or lower, the fluidity will generally decrease, which is not preferable. The cooling step is preferably carried out by bringing the jet of the high-temperature heavy oil mixture and the jet of the circulating oil into countercurrent contact or collision. In this way, the high-temperature heavy oil mixture is rapidly cooled by the collision movement of the circulating oil and the heavy oil mixture, and the temperature conditions necessary for the generation of insoluble substances are satisfied, and the collision of the precipitated insolubles is prevented. Therefore, aggregation of insoluble matter is promoted. On the other hand, the insoluble substances precipitated and aggregated in this manner are successively separated and removed, and continuous preparation of raw material oil for gasoline production is achieved. [Specific Description of the Invention] Hereinafter, the method of the present invention will be explained in more detail based on preferred specific examples thereof. FIG. 2 is a layout diagram of the main parts of an apparatus used to carry out the method of the present invention, and FIG. 3 is an overall layout diagram including the main parts shown in FIG. As shown in FIGS. 2 and 3, the apparatus for carrying out the method of the present invention comprises an upper tank 1 and a lower tank 2 having substantially the same diameter and arranged substantially vertically. 1/2 to 1/10 preferably 1/5 to 1/ of the diameter of
They are connected by a relatively small cylindrical tube 3 having a diameter of 6. A single heavy oil introduction pipe 4 is introduced into the lower tank 2 by penetrating its side wall, and its downstream end opens upward toward the cylindrical pipe 3 within the lower tank 2.
Further, the upstream side of the introduction pipe 4 branches relatively close to the lower tank 2 into introduction pipes 4a and 4b for the raw material heavy oil, and these introduction pipes 4a and 4b are connected to heaters 5a and 5b, respectively. , the raw material heavy oil tank 7 via the pump 6a or 6b.
It is bonded to a or 7b. Further, a heavy liquid extraction pipe 8 is connected to the bottom of the lower tank 2, and this extraction pipe 8 is connected to a heavy liquid tank 10 via a pump 9. On the other hand, a light liquid extraction pipe 11 is connected to the upper part of the upper tank 1, and this extraction pipe 11 is connected to a product oil tank 14 via a receiving tank 12 and a pump 13. Further, a circulation pipe 15 is branched and connected downstream of the pump 13 of the extraction pipe 11.
5 extends into the upper tank 1 and opens downward toward the cylindrical pipe 3 within the upper tank 1. A cooler 16 is disposed in the middle of this circulation pipe 15. Also upper tank 1
Inside, from one side wall to the opposite side wall,
A plurality of substantially horizontal shelves 17 extend, the lower ones of which extend beyond the center of the tank 1 toward the opposite side walls. Moreover, heaters 20a and 20b are arranged around the bottoms of the tanks 1 and 2. Next, a typical embodiment of preparing raw material oil for gasoline production using the above-mentioned apparatus will be described.
In the following description, "parts" and "%" are based on weight unless otherwise specified. First, heavy oil A with relatively low aroma is pumped from tank 7a, and heavy oil B with relatively high aroma is pumped from tank 7b with pump 6a or 6b, respectively.
200 to 390 by heater 5a or 5b.
After heating to ℃, the two liquids are mixed just before the lower tank 2, and the two liquids are mixed through the introduction pipe 4 into the lower tank 2.
It flows out or spouts directly below the inner cylindrical pipe 3. The heavy oil A is, for example, petroleum-based normal pressure or vacuum direct distillation residue oil, and the heavy oil B is, for example,
Coal tar, petroleum naphtha cracking residue oil, thermal cracking residue oil, hydrocracking residue oil, etc. are used. It is preferable to use the heavy oil B in an amount of 30 to 70 parts per 100 parts of the mixed oil in consideration of the removal efficiency of insoluble substances and the properties of the product raw material oil. The introduced high-temperature heavy oil mixture mainly rises through the cylindrical pipe 3 and passes through the circulation pipe 15 and the cooler 1.
By contact or collision with the circulating light liquid (50 to 90°C) flowing out through 6, it is preferably cooled to below 100°C, and the insoluble substances generated by this series of mixing and cooling are promoted to flocculate and settle. ,
It flows down through the cylindrical pipe 3 in contact with the heavy oil mixture and is deposited at the bottom of the lower tank 2. The heavy liquid, which mainly consists of deposited insoluble substances, is heated by the heater 20b and flows into the bottom pipe 8 while maintaining its fluidity.
is extracted from the heavy liquid tank 10 via a pump 9.
will be put on hold. On the other hand, the light liquid from which insoluble substances have been removed in the upper tank 1 further passes between the shelves 17 and rises, further separating the insoluble substances, and is extracted from the upper part of the upper tank 1 through the piping 11, and is then drawn out from the upper tank 1 through the pipe 11, The product oil is stored in a product oil tank 14 via a pump 13. Further, a part of the light liquid coming out of the pump 13 is circulated to the upper tank 1 via the piping 15, and is made to flow out under the shelf plate 17 in the upper tank 1. In the above, a preferred example of the method of the present invention and its operation mode have been explained based on a specific apparatus. However, it will be readily apparent to those skilled in the art that various modifications to the above example method may be made within the scope of the present invention. For example, the raw material heavy oil is not limited to two types, but three or more types can be used. Furthermore, it is preferable that the introduction pipe 4 for the raw material heavy oil is extended into the lower tank 2 and opened directly below the cylindrical pipe 3, but the invention is not limited thereto. is obtained. The introduction pipe 4 is not limited to a single pipe, but a plurality of introduction pipes can be connected to the lower tank 2 or extended into the lower tank 2 for each raw material heavy oil. Furthermore, although the shelf board 17 in the upper tank 1 has the effect of promoting separation of the light liquid and insoluble substances, it may be tilted diagonally downward in order to prevent the insoluble substances from depositing on the shelf board 17. preferable. In the above example, the volumes of the upper tank 1 and the lower tank 2 are approximately the same, but the ratio can be changed as appropriate in consideration of mixing and separation. According to the method described above, raw oils are mixed in pipes at high temperatures (line blending),
Furthermore, since the cooling and deposition can be carried out in a tank with a relatively large capacity, there is no problem of clogging of piping by insoluble substances produced. Furthermore, by circulating a portion of the product light liquid, etc., a temperature difference necessary for mixing and separation is provided, and these temperatures can be easily set and controlled. EXAMPLES OF THE INVENTION The following is an example of the actual operation of an example of an apparatus used in the method of the invention essentially shown in FIGS. 2 and 3. Although the following examples are relatively small-scale examples, they are believed to provide a sufficient understanding of the effectiveness of the method of the present invention. Raw material oil for gasoline production was produced using petroleum-based heavy oil A, ethylene tar petroleum cracking heavy oil B, and coal-based heavy oil C having properties shown in Table 1 below as raw material heavy oils. Example 1 Heavy oil A was fed at a rate of 140 g/min and heavy oil B at a rate of 60 g/min from feed pumps 6a and 6b, heated to 200°C by heaters 5a and 5b, respectively, and then pipes 4a, From 4b to lower tank 2 (diameter approx. 250mm, 40
) and flowed out from a position 100 mm directly below the lower end of the cylindrical pipe 3 (diameter approximately 50 mm, length 200 mm) in the lower tank 2. The blending ratio of heavy oil A and heavy oil B was A:B=70:30. On the other hand, under the shelf of the upper tank 1 (about 300 mm in diameter) equipped with shelf boards 17 (total of 5) as shown, piping 15,
The light liquid at a temperature of about 80°C was circulated through the cooler 16 at a rate of 1/min and contacted with the jet of the heavy oil mixture to rapidly cool the heavy oil mixture to a temperature below 100°C. The light liquid extracted from the upper tank 1 is collected at a rate of 166 g/min (yield 83%) in the storage tank 14, while it is heated to about 200°C and flows from the bottom pipe 8 of the lower tank 2. A heavy liquid, consisting mainly of insoluble materials, was recovered. The metal content and properties of the recovered light liquid and heavy liquid were as shown in Table 1. Example 2 Using heavy oil A and heavy oil C, light liquid and heavy liquid were recovered from a heavy oil mixture in the same manner and under the same conditions as in Example 1 above, and their metal content and properties were analyzed. The analysis results were as shown in Table 1. Comparative Example Heavy oil A was deasphalted by a solvent deasphalting method using Normanheptane as a solvent according to a conventional method,
The metal content and properties of the obtained light liquid were analyzed. The analysis results were as shown in Table 1. As is clear from the above analysis results, the light liquids obtained in Example 1 and Example 2 according to the method of the present invention have superior metal removal effects compared to the comparative example, and in particular,
To promote coking in the catalytic cracking process,
It can be seen that the Ni component, which causes a decrease in catalyst activity, is removed extremely effectively.
上述したように、本発明によれば、二種以上の
重質油を混合し、生成する金属成分を含有する不
溶性物質を分離除去して、ガソリンの製造に適し
た原料油を連続的に調製するための方法が提供さ
れ、この方法によれば、下記のようなすぐれた効
果が得られる。
(イ) 従来法のように、脱金属、脱アスフアルテン
の手段として、溶剤や触媒を一切使用する必要
がないので、製造工程が簡易化され、かつ、製
造条件の設定、制御が容易であり、技術的にす
ぐれているとともに経済的に有利である。
(ロ) 一連の連続的操作によつて効率的に、重質油
中の金属成分、アスフアルテンを除去すること
ができるので、従来のバツチプロセスに比べ生
産性の点で有利であり、またバツチ毎に品質が
変化する等の問題が解消されるので品質の安定
化、信頼性の点でもすぐれている。
(ハ) 製品油を一部循環させて重質油混合物の流れ
と流動的に接触させるようにしたので、循環油
と重質油混合物とが衝突する運動により不溶性
物質の生成に必要な温度条件が満足されるとと
もに(冷却効果)、不溶性物質の析出と衝突、
凝集が促進されるという相乗的効果が発揮され
る。
As described above, according to the present invention, two or more types of heavy oils are mixed and the resulting insoluble substances containing metal components are separated and removed to continuously prepare feedstock oil suitable for gasoline production. According to this method, the following excellent effects can be obtained. (b) Unlike conventional methods, there is no need to use any solvent or catalyst as a means of demetallization or asphaltene removal, so the manufacturing process is simplified, and manufacturing conditions can be easily set and controlled; It is technically superior and economically advantageous. (b) Metal components and asphaltenes in heavy oil can be efficiently removed through a series of continuous operations, which is advantageous in terms of productivity compared to conventional batch processes, and Since problems such as changes in quality are resolved, it is also excellent in terms of quality stability and reliability. (c) Since a part of the product oil is circulated so that it comes into fluid contact with the flow of the heavy oil mixture, the temperature conditions necessary for the generation of insoluble substances due to the collision motion between the circulating oil and the heavy oil mixture is satisfied (cooling effect), precipitation and collision of insoluble substances,
A synergistic effect of promoting aggregation is exerted.
第1図は本発明方法の概要を示す工程図であ
り、第2図は本発明の方法の実施に用いる装置の
一実施例の要部配置図であり、第3図は第2図図
示の要部を含む全体配置図である。
1……上槽、2……下槽、3……筒管、4……
重質油混合導入管、4a,4b……重質油の導入
分岐管、8……重液抜出管、11……軽液抜出
管、15……軽液循環配管、16……冷却器、1
7……棚板。
FIG. 1 is a process diagram showing an overview of the method of the present invention, FIG. 2 is a layout diagram of main parts of an embodiment of the apparatus used for carrying out the method of the present invention, and FIG. It is an overall layout diagram including main parts. 1... Upper tank, 2... Lower tank, 3... Cylindrical pipe, 4...
Heavy oil mixing introduction pipe, 4a, 4b... Heavy oil introduction branch pipe, 8... Heavy liquid extraction pipe, 11... Light liquid extraction pipe, 15... Light liquid circulation piping, 16... Cooling vessel, 1
7...Shelf board.
Claims (1)
油混合物を調製し、さらにこの混合物を冷却する
ことにより重質油混合物中に不溶性物質を生成さ
せ、この不溶性物質を重質油混合物から除去する
ことによりガソリン製造用原料油を連続的に製造
するに際し、製造されたガソリン製造用原料油の
一部を抜出して前記冷却工程に循環させ、この循
環油の流れと前記高温の重質油混合物の流れを接
触させることにより重質油混合物の冷却を行うこ
とを特徴とする、ガソリン製造用原料油の連続製
造法。 2 高温の重質油混合物の温度が200〜390℃であ
りさらにその冷却を100℃以下の温度で行なう、
特許請求の範囲第1項に記載の方法。 3 高温の重質油混合物の噴流と循環油の噴流と
を向流衝突させることにより重質油混合物の冷却
を行う、特許請求の範囲第1項に記載の方法。 4 循環油と重質油混合物とを接触させる前に、
あらかじめ循環油を約50〜約90℃に冷却する、特
許請求の範囲第1項に記載の方法。 5 少なくとも二種の重質油をあらかじめ各々加
熱したのちにこれらを合流させることにより高温
重質油混合物を調整する、特許請求の範囲第1項
に記載の方法。 6 少なくとも二種の重質油が、石油系の常圧な
いし減圧直留残渣油、コールタール、ナフサ分解
残渣油、熱分解残渣油および水素化分解残渣油か
らなる群から選ばれる、特許請求の範囲第1項に
記載の方法。[Claims] 1. An insoluble substance is produced in the heavy oil mixture by preparing a high-temperature heavy oil mixture consisting of at least two types of heavy oil, and further cooling this mixture, and the insoluble substance is When continuously producing feedstock oil for gasoline production by removing it from a heavy oil mixture, a part of the produced feedstock oil for gasoline production is extracted and circulated to the cooling process, and the flow of this circulating oil and the 1. A continuous production method for raw material oil for gasoline production, characterized in that a heavy oil mixture is cooled by contacting a stream of a high-temperature heavy oil mixture. 2. The temperature of the high-temperature heavy oil mixture is 200 to 390°C, and further cooling is performed at a temperature of 100°C or less,
A method according to claim 1. 3. The method according to claim 1, wherein the heavy oil mixture is cooled by countercurrently colliding a jet of the hot heavy oil mixture with a jet of circulating oil. 4. Before bringing the circulating oil into contact with the heavy oil mixture,
2. The method of claim 1, wherein the circulating oil is previously cooled to about 50 to about 90<0>C. 5. The method according to claim 1, wherein the high-temperature heavy oil mixture is prepared by heating at least two types of heavy oil in advance and then combining them. 6. The claimed invention, wherein the at least two types of heavy oils are selected from the group consisting of petroleum-based atmospheric or vacuum direct distillation residue oil, coal tar, naphtha cracking residue oil, thermal cracking residue oil, and hydrocracking residue oil. The method described in Scope No. 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21652684A JPS6198794A (en) | 1984-10-16 | 1984-10-16 | Continuous production of stock oil for producing gasoline |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21652684A JPS6198794A (en) | 1984-10-16 | 1984-10-16 | Continuous production of stock oil for producing gasoline |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6198794A JPS6198794A (en) | 1986-05-17 |
| JPH0115558B2 true JPH0115558B2 (en) | 1989-03-17 |
Family
ID=16689808
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP21652684A Granted JPS6198794A (en) | 1984-10-16 | 1984-10-16 | Continuous production of stock oil for producing gasoline |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6198794A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8083930B2 (en) | 2006-08-31 | 2011-12-27 | Exxonmobil Chemical Patents Inc. | VPS tar separation |
| WO2008027139A1 (en) | 2006-08-31 | 2008-03-06 | Exxonmobil Chemical Patents Inc. | Method for upgrading steam cracker tar using pox /cocker |
| WO2008027131A1 (en) | 2006-08-31 | 2008-03-06 | Exxonmobil Chemical Patents Inc. | Disposition of steam cracked tar |
| US7846324B2 (en) | 2007-03-02 | 2010-12-07 | Exxonmobil Chemical Patents Inc. | Use of heat exchanger in a process to deasphalt tar |
-
1984
- 1984-10-16 JP JP21652684A patent/JPS6198794A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6198794A (en) | 1986-05-17 |
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