JPH0823024B2 - Method for removing mercury in hydrocarbon oils - Google Patents

Method for removing mercury in hydrocarbon oils

Info

Publication number
JPH0823024B2
JPH0823024B2 JP63012290A JP1229088A JPH0823024B2 JP H0823024 B2 JPH0823024 B2 JP H0823024B2 JP 63012290 A JP63012290 A JP 63012290A JP 1229088 A JP1229088 A JP 1229088A JP H0823024 B2 JPH0823024 B2 JP H0823024B2
Authority
JP
Japan
Prior art keywords
mercury
hydrocarbon
oil
copper
liquid
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 - Lifetime
Application number
JP63012290A
Other languages
Japanese (ja)
Other versions
JPH01188589A (en
Inventor
隆 鳥畑
悦子 川島
Original Assignee
三井石油化学工業株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 三井石油化学工業株式会社 filed Critical 三井石油化学工業株式会社
Priority to JP63012290A priority Critical patent/JPH0823024B2/en
Priority to AU28619/89A priority patent/AU607037B2/en
Priority to CA000588678A priority patent/CA1325992C/en
Priority to US07/299,025 priority patent/US4946582A/en
Priority to EP89300567A priority patent/EP0325486B1/en
Priority to AT89300567T priority patent/ATE78861T1/en
Priority to DE8989300567T priority patent/DE68902239T2/en
Priority to ES198989300567T priority patent/ES2034604T3/en
Priority to KR1019890000630A priority patent/KR910005348B1/en
Priority to CN 89101058 priority patent/CN1015471B/en
Publication of JPH01188589A publication Critical patent/JPH01188589A/en
Priority to GR920402104T priority patent/GR3005782T3/el
Publication of JPH0823024B2 publication Critical patent/JPH0823024B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P30/00Technologies relating to oil refining and petrochemical industry
    • Y02P30/40Ethylene production

Description

【発明の詳細な説明】 <産業上の利用分野> 本発明は、炭化水素系油中に混在する水銀の除去方法
に関し、特に、銅化合物を利用した水銀の選択的、効率
的除去方法に関する。
TECHNICAL FIELD The present invention relates to a method for removing mercury mixed in a hydrocarbon oil, and more particularly to a method for selectively and efficiently removing mercury using a copper compound.

<従来の技術> 水添等によって、ナフサ等の炭化水素系油を改質する
場合には、パラジウム担持アルミナ系等の触媒が用いら
れる。ところが炭化水素系油中に不純物として水銀が存
在すると、触媒が被毒して反応が充分行われない。
<Prior Art> When reforming a hydrocarbon oil such as naphtha by hydrogenation or the like, a palladium-supported alumina catalyst or the like is used. However, when mercury is present as an impurity in the hydrocarbon oil, the catalyst is poisoned and the reaction is not sufficiently carried out.

このため、従来から以下のような水銀の除去方法が行
われている。
Therefore, the following mercury removal methods have been conventionally performed.

a)活性炭、モレキュラシーブ、シリカゲル、ゼオライ
ト、アルミナ等の多孔質吸着剤を用いる物理吸着方法。
a) Physical adsorption method using a porous adsorbent such as activated carbon, molecular sieve, silica gel, zeolite or alumina.

b)金属硫化物、あるいは多孔質吸着剤に硫黄を添加
し、水銀と硫黄との反応/吸着によって水銀を除去する
方法。
b) A method in which sulfur is added to a metal sulfide or a porous adsorbent and mercury is removed by a reaction / adsorption of mercury and sulfur.

しかし、a)の物理吸着方法では、炭化水素系油中の
重質分やガム質は効率良く除去されるものの、水銀の除
去率は30〜70wt%と低い。また、(b)の反応/吸着方
法では、反応/吸着後の濾別が困難であると同時に、
a)の物理吸着方法と同様水銀の除去率が低い。
However, in the physical adsorption method of a), although the heavy components and gums in the hydrocarbon-based oil are efficiently removed, the removal rate of mercury is as low as 30 to 70 wt%. Further, in the reaction / adsorption method (b), it is difficult to filter after the reaction / adsorption, and at the same time,
The mercury removal rate is low as in the physical adsorption method a).

このため、炭化水素系油中の水銀を選択的かつ効率良
く除去する方法が望まれている。
Therefore, a method for selectively and efficiently removing mercury in hydrocarbon-based oil is desired.

<発明が解決しようとする課題> 本発明の目的は、炭化水素系油中の微量の水銀を選択
的かつ効率的良く除去する方法を提供しようとするにあ
る。
<Problems to be Solved by the Invention> An object of the present invention is to provide a method for selectively and efficiently removing a trace amount of mercury in a hydrocarbon oil.

<課題を解決するための手段> 本発明は、炭化水素系油中に含まれる微量の水銀を除
去する方法であって、炭化水素系油を、銅のハロゲン化
物と接触させることを特徴とする炭化水素系油中の水銀
の除去方法を提供する。
<Means for Solving the Problems> The present invention is a method for removing a trace amount of mercury contained in a hydrocarbon-based oil, which is characterized in that the hydrocarbon-based oil is brought into contact with a halide of copper. Provided is a method for removing mercury in a hydrocarbon oil.

ここで、前記銅のハロゲン化物が、水溶液または粉末
であるのが良い。
Here, the copper halide is preferably an aqueous solution or powder.

また、前記銅のハロゲン化物が、ハロゲン化第1銅お
よび/またはハロゲン化第2銅であるのが好ましい。
Further, it is preferable that the copper halide is a cuprous halide and / or a cupric halide.

<発明の構成> 以下に本発明の構成を詳述する。<Structure of the Invention> The structure of the present invention will be described in detail below.

本発明方法を適用する炭化水素系油は、常温で液体の
炭化水素であればいかなるものでもよい。
The hydrocarbon-based oil to which the method of the present invention is applied may be any hydrocarbon as long as it is a liquid hydrocarbon at room temperature.

炭化水素系油としては、原油、直留ナフサ、灯油、軽
油、減圧留出物、常圧残存油、エチレンプラントの熱分
解装置で副生される熱分解ガソリン、熱処理を受けた炭
化水素系油、接触分解装置で生成されたナフサ留分、リ
サイクル油などが例示される。
Hydrocarbon-based oils include crude oil, straight-run naphtha, kerosene, light oil, vacuum distillate, atmospheric residual oil, pyrolysis gasoline by-produced in a thermal cracker of an ethylene plant, hydrocarbon-based oil that has been heat-treated. Examples thereof include naphtha fraction produced by a catalytic cracking device and recycled oil.

特に、天然ガスより液化石油ガス(LPG)を除いたnat
ural gas liquid(NGL)、ことにNGL中でも高沸点成分
を含むHeavy natural gas liquid(重質天然ガスリキッ
ド)中の銀除去に好適に用いられる。
In particular, nat excluding liquefied petroleum gas (LPG) from natural gas
Suitable for removing silver in ural gas liquid (NGL), especially heavy natural gas liquid containing high boiling point components in NGL.

本発明方法では、除去される炭化水素系油中の水銀の
存在形態は、単体水銀、無機水銀、有機水銀等いかなる
形態で存在してもよいが、常温で液体である炭化水素系
油中に存在する有機水銀に対して特に有効である。
In the method of the present invention, the existing form of mercury in the hydrocarbon-based oil to be removed may be any form such as elemental mercury, inorganic mercury, and organic mercury, but in the hydrocarbon-based oil that is liquid at room temperature. It is particularly effective against the organic mercury present.

炭化水素系油中の水銀濃度は、特に限定されるもので
はないが、400〜600PPb以下、好ましくは100〜150PPb以
下であると反応効率が良い。
The concentration of mercury in the hydrocarbon oil is not particularly limited, but the reaction efficiency is good when it is 400 to 600 PPb or less, preferably 100 to 150 PPb or less.

必要な場合は、炭化水素系油中のスラッジ等を、あら
かじめ濾過膜やフィルター等で濾過し、スラッジととも
に濾別される水銀を除去しておくのが良い。
If necessary, it is advisable to previously filter the sludge in the hydrocarbon-based oil with a filter membrane or a filter to remove the mercury that is filtered off together with the sludge.

本発明の方法は、水銀を含む炭化水素系油に、銅のハ
ロゲン化物を以下の状態で接触させて処理を行う方法で
ある。銅のハロゲン化物(以下、「銅化合物」と略
す。)は、好ましくは下記の化合物またはこれらの混合
物を下記の状態で用いることができる。
The method of the present invention is a method in which a hydrocarbon halide oil containing mercury is brought into contact with a halide of copper in the following state to perform treatment. As the copper halide (hereinafter abbreviated as “copper compound”), the following compounds or mixtures thereof can be preferably used in the following states.

(1)銅化合物溶液を炭化水素系油と液−液接触する。(1) Liquid-liquid contact of a copper compound solution with a hydrocarbon-based oil.

ハロゲン化銅溶液、特にCuCl、CnCl2の塩酸、塩化ア
ルカリまたはアンモニア水溶液、CuCl2の水溶液等を炭
化水素系油中に添加する。
A copper halide solution, in particular, CuCl, CnCl 2 hydrochloric acid, an aqueous solution of alkali chloride or ammonia, an aqueous solution of CuCl 2 or the like is added to the hydrocarbon oil.

銅化合物濃度は10ppm以上、例えば10ppm〜40wt%、好
ましくは0.5〜10wt%が好ましい。
The copper compound concentration is 10 ppm or more, for example, 10 ppm to 40 wt%, preferably 0.5 to 10 wt%.

(2)銅化合物粉末を炭化水素系油中に加える。(2) Copper compound powder is added to hydrocarbon-based oil.

ハロゲン化銅、酸化銅、特にCuCl、CuCl2粉末を炭化
水素系油と接触させる。
Copper halide, copper oxide, especially CuCl, CuCl 2 powder is contacted with a hydrocarbon oil.

銅化合物と炭化水素系油との接触方法は以下の反応装
置等を用いるのが好ましいが、これらに限定されない。
The method of contacting the copper compound and the hydrocarbon oil is preferably, but not limited to, the following reaction device.

第1図には、撹拌器11を備えた反応槽3を有する装置
を示す。
FIG. 1 shows an apparatus having a reaction tank 3 equipped with a stirrer 11.

反応槽3には、原料1を供給するラインと、銅化合物
2を供給するラインが設けられ、反応槽3は、静置槽4
と流体連通している。
The reaction tank 3 is provided with a line for supplying the raw material 1 and a line for supplying the copper compound 2, and the reaction tank 3 is a stationary tank 4
Is in fluid communication with.

静置槽4には、精製品取出ライン9と水銀処理ライン
10のそれぞれの排出口が設けられる。
The stationary tank 4 has a purified product extraction line 9 and a mercury treatment line.
Ten respective outlets are provided.

水銀処理ライン10は、一方で弁7を介して図示しない
水銀処理装置へ連通し、他方で弁8とポンプ6を介して
反応槽3へ連通する。
The mercury treatment line 10 communicates with a mercury treatment device (not shown) via the valve 7 on the one hand, and communicates with the reaction tank 3 via the valve 8 and the pump 6 on the other hand.

炭化水素系油等の原料1は、反応槽3へ供給され、他
方から銅化合物2が溶液あるいは粉末状で反応槽3へ供
給される。
A raw material 1 such as a hydrocarbon oil is supplied to the reaction tank 3, and the copper compound 2 is supplied to the reaction tank 3 from the other side in a solution or powder form.

反応槽3内で、炭化水素系油と銅化合物は撹拌器11で
充分混合される。
In the reaction tank 3, the hydrocarbon oil and the copper compound are thoroughly mixed by the stirrer 11.

混合液は静置槽4へ移送され、静置されて精製液13と
水銀含有相14に分離され、精製液13は精製品取出ライン
9より取出される。一方水銀含有相14は、弁7を介して
図示しない水銀処理装置へ移送されて排出される。
The mixed liquid is transferred to the stationary tank 4 and allowed to stand still to be separated into the purified liquid 13 and the mercury-containing phase 14, and the purified liquid 13 is taken out from the purified product take-out line 9. On the other hand, the mercury-containing phase 14 is transferred to the mercury treatment device (not shown) via the valve 7 and discharged.

水銀を除かれた残部の液相は、必要により弁8を介し
て、ポンプ6により反応槽3に回収される。
The remaining liquid phase from which mercury has been removed is recovered in the reaction tank 3 by the pump 6 via the valve 8 if necessary.

第2図は、銅化合物2が原料1と混合された後、ポン
プ7により移送される装置を示す。原料1と銅化合物2
は、ポンプ7により移送される途中で充分混合され接触
するので、第1図のように撹拌器を備えた反応槽を設け
る必要はない。必要により第2図に示す多段の静置槽
4、12を設けて、第1図と同様に精製液13と水銀含有相
14とを分離する。
FIG. 2 shows an apparatus in which the copper compound 2 is mixed with the raw material 1 and then transferred by the pump 7. Raw material 1 and copper compound 2
Since they are sufficiently mixed and come into contact with each other while being transferred by the pump 7, it is not necessary to provide a reaction vessel equipped with an agitator as shown in FIG. If necessary, the multistage stationary tanks 4 and 12 shown in FIG. 2 are provided, and the purified liquid 13 and the mercury-containing phase are provided as in FIG.
Separate from 14

<実施例> 以下に本発明を実施例により具体的に説明する。<Examples> The present invention will be specifically described below with reference to Examples.

(実施例1、2) heavy natural gas liquid(重質天然ガスリキッド)
100mlを0.2μmのミリポアフィルターで濾過した。濾
別したスラッジ組成は下記であった。
(Examples 1 and 2) heavy natural gas liquid (heavy natural gas liquid)
100 ml was filtered through a 0.2 μm Millipore filter. The sludge composition filtered out was as follows.

Fe 10.0wt% Si 18.3wt% Hg 3.1wt% S 2.3wt% 濾液中の水銀濃度は約130PPbであった。 Fe 10.0 wt% Si 18.3 wt% Hg 3.1 wt% S 2.3 wt% The mercury concentration in the filtrate was about 130 PPb.

濾液中に表1の濃度で銅化合物を加え、充分撹拌し、
静置1時間後の精製液中の水銀濃度を測定し、結果を表
1に示した。
A copper compound was added to the filtrate at the concentration shown in Table 1 and stirred sufficiently,
The mercury concentration in the purified liquid after 1 hour of standing was measured, and the results are shown in Table 1.

(実施例3、4) 実施例1、2で得られたと同様の濾液100ml中に、表
1に示すCuCl、CuCl2の各化合物1.0gを加え、充分撹拌
し、静置1時間後の精製液中の水銀濃度を測定し、結果
を表1に示した。
(Examples 3 and 4) To 100 ml of the same filtrate as obtained in Examples 1 and 2, 1.0 g of each compound of CuCl and CuCl 2 shown in Table 1 was added, stirred sufficiently, and allowed to stand for 1 hour for purification. The mercury concentration in the liquid was measured, and the results are shown in Table 1.

(比較例1〜3) べつに比較として、実施例と同様のheavy natural ga
s liquid(重質天然ガスリキッド)からスラッジを除去
した濾液中に、表1に示すFeCl2、FeCl3、PbCl2をそれ
ぞれ実施例と同様に加え、同様にして得た精製液中の水
銀濃度を測定し、結果を表1に示した。
(Comparative Examples 1 to 3) As a comparison, heavy natural ga
FeCl 2 , FeCl 3 , and PbCl 2 shown in Table 1 were added to the filtrate obtained by removing sludge from s liquid (heavy natural gas liquid) in the same manner as in Examples, and the mercury concentration in the purified liquid obtained in the same manner Was measured and the results are shown in Table 1.

<発明の効果> 本発明方法は、銅化合物を用いて炭化水素系油中の水
銀と接触させるので、炭化水素系油中に混在する水銀が
選択的に効率良く除去できる。
<Effects of the Invention> In the method of the present invention, since the copper compound is used to bring it into contact with mercury in the hydrocarbon-based oil, mercury mixed in the hydrocarbon-based oil can be selectively and efficiently removed.

水銀を除去された炭化水素系油は、触媒被毒成分を含
まないので、水添反応等の触媒使用反応に広く利用でき
る。
Since the hydrocarbon-based oil from which mercury has been removed does not contain a catalyst poisoning component, it can be widely used for a reaction using a catalyst such as a hydrogenation reaction.

【図面の簡単な説明】[Brief description of drawings]

第1図は、本発明方法を実施する装置の1例を示す線図
である。 第2図は、本発明方法を実施する装置の他の例を示す線
図である。 符号の説明 1……原料、 2……銅化合物、 3……反応槽、 4……静置槽、 5……配管、 6……ポンプ、 7、8……弁、 9……精製品取出ライン、 10……水銀処理ライン、 11……撹拌器、 13……精製液、 14……水銀含有相
FIG. 1 is a diagram showing an example of an apparatus for carrying out the method of the present invention. FIG. 2 is a diagram showing another example of an apparatus for carrying out the method of the present invention. Explanation of symbols 1 ... Raw material, 2 ... Copper compound, 3 ... Reaction tank, 4 ... Stationary tank, 5 ... Piping, 6 ... Pump, 7, 8 ... Valve, 9 ... Purified product removal Line, 10 ... Mercury processing line, 11 ... Stirrer, 13 ... Purified liquid, 14 ... Mercury-containing phase

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 // B01J 20/02 A ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 6 Identification code Office reference number FI technical display area // B01J 20/02 A

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】炭化水素系油中に含まれる微量の水銀を除
去する方法であって、炭化水素系油を、銅のハロゲン化
物と接触させることを特徴とする炭化水素系油中の水銀
の除去方法。
1. A method for removing a trace amount of mercury contained in a hydrocarbon-based oil, which comprises contacting the hydrocarbon-based oil with a copper halide. Removal method.
【請求項2】前記銅のハロゲン化物が、水溶液または粉
末である特許請求の範囲第1項に記載の炭化水素系油中
の水銀の除去方法。
2. The method for removing mercury in a hydrocarbon oil according to claim 1, wherein the copper halide is an aqueous solution or powder.
【請求項3】前記銅のハロゲン化物が、ハロゲン化第1
銅および/またはハロゲン化第2銅である特許請求の範
囲第1項または第2項に記載の炭化水素系油中の水銀の
除去方法。
3. The copper halide is a halogenated first
The method for removing mercury in a hydrocarbon oil according to claim 1 or 2, which is copper and / or cupric halide.
JP63012290A 1988-01-22 1988-01-22 Method for removing mercury in hydrocarbon oils Expired - Lifetime JPH0823024B2 (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
JP63012290A JPH0823024B2 (en) 1988-01-22 1988-01-22 Method for removing mercury in hydrocarbon oils
AU28619/89A AU607037B2 (en) 1988-01-22 1989-01-19 Method of removing mercury from hydrocarbon oils
CA000588678A CA1325992C (en) 1988-01-22 1989-01-19 Method of removing mercury from hydrocarbon oils
US07/299,025 US4946582A (en) 1988-01-22 1989-01-19 Method of removing mercury from hydrocarbon oils
ES198989300567T ES2034604T3 (en) 1988-01-22 1989-01-20 A METHOD OF ELIMINATION OF MERCURY FROM A HYDROCARBON OIL.
AT89300567T ATE78861T1 (en) 1988-01-22 1989-01-20 PROCESS FOR REMOVAL OF MERCURY FROM HYDROCARBON OILS.
DE8989300567T DE68902239T2 (en) 1988-01-22 1989-01-20 METHOD FOR REMOVING MERCURY FROM HYDROCARBON OILS.
EP89300567A EP0325486B1 (en) 1988-01-22 1989-01-20 Method of removing mercury from hydrocarbon oils
KR1019890000630A KR910005348B1 (en) 1988-01-22 1989-01-21 Method of removing mercury from hydrocarbon oils
CN 89101058 CN1015471B (en) 1988-01-22 1989-01-21 Method of removing mercury from hydrocarbon oils
GR920402104T GR3005782T3 (en) 1988-01-22 1992-09-24

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63012290A JPH0823024B2 (en) 1988-01-22 1988-01-22 Method for removing mercury in hydrocarbon oils

Publications (2)

Publication Number Publication Date
JPH01188589A JPH01188589A (en) 1989-07-27
JPH0823024B2 true JPH0823024B2 (en) 1996-03-06

Family

ID=11801213

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63012290A Expired - Lifetime JPH0823024B2 (en) 1988-01-22 1988-01-22 Method for removing mercury in hydrocarbon oils

Country Status (1)

Country Link
JP (1) JPH0823024B2 (en)

Also Published As

Publication number Publication date
JPH01188589A (en) 1989-07-27

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