JP5070169B2 - 炭化水素油の製造方法 - Google Patents
炭化水素油の製造方法 Download PDFInfo
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- C10G3/00—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
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- C10G3/45—Catalytic treatment characterised by the catalyst used containing iron group metals or compounds thereof
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- C10G3/00—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
- C10G3/42—Catalytic treatment
- C10G3/44—Catalytic treatment characterised by the catalyst used
- C10G3/48—Catalytic treatment characterised by the catalyst used further characterised by the catalyst support
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- C10G3/50—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids in the presence of hydrogen, hydrogen donors or hydrogen generating compounds
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- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/02—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
- C10G45/04—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G67/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only
- C10G67/02—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only
- C10G67/10—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only including alkaline treatment as the refining step in the absence of hydrogen
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1011—Biomass
- C10G2300/1014—Biomass of vegetal origin
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1011—Biomass
- C10G2300/1018—Biomass of animal origin
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/201—Impurities
- C10G2300/202—Heteroatoms content, i.e. S, N, O, P
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/40—Characteristics of the process deviating from typical ways of processing
- C10G2300/4018—Spatial velocity, e.g. LHSV, WHSV
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- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/20—Technologies relating to oil refining and petrochemical industry using bio-feedstock
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- Chemical & Material Sciences (AREA)
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- Chemical Kinetics & Catalysis (AREA)
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- Crystallography & Structural Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
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Description
(C17H35COO)3(C3H5)+12H2→3C18H38+6H2O+C3H6 (1)
(C17H35COO)3(C3H5)+2H2→C17H36+3CO2+C3H6 (2)
PW<6.11×10^{7.5×T÷(T+237.3)}×10−4 (3)
で表される条件を満たすように温度をコントロールすればよい。
PW=P×MW÷(MW+MH+MP) (4)
で表される。
PW=5×(6×C)÷{6×C+(23.0×100−12×C)+1×C} (5)
で表される。従って、原料の性状、水素油比および反応圧力に応じて式(5)の反応率に応じた温度制御をすることで生成した水の凝縮を防止することができる。
濃度5質量%のアルミン酸ナトリウム水溶液に水ガラス3号を加え、65℃に保温した容器に入れた。他方、65℃に保温した別の容器において濃度2.5質量%の硫酸アルミニウム水溶液にリン酸(濃度85%)を加えた溶液を調製し、これに前述のアルミン酸ナトリウムを含む水溶液を滴下した。混合溶液のpHが7.0になる時点を終点とし、得られたスラリー状の生成物をフィルターに通して濾取し、ケーキ状のスラリーを得た。
以下の実施例及び比較例では、下記の固定商流通式反応装置A、Bを用いた。
<固定床流通式反応装置A>
電気ヒーターで加熱できる反応管(内径20mm)の上流に原料送液ポンプ、水素供給装置及び配管を、下流に冷却器、L字型配管、圧力調節弁の順で配置し、その先を常圧ガスセパレータ設置したものを固定床流通式反応装置Aとする。なお、接液部の材質は全てSUS316である。
<固定床流通式反応装置B>
反応管と冷却器の間に薬剤注入部を設けて反応管から薬剤注入部までの間をヒーター加熱とした以外は固定床流通式反応装置Aと同様としたものを固定床流通式反応装置Bとする。なお、接液部の材質は全てSUS316である。
触媒の50mlを充填した反応管を固定床流通式反応装置Aに取り付けた。次いで、ジメチルジサルファイドを加えた直留軽油(硫黄分3質量%)を用いて触媒層平均温度300℃、水素分圧6MPa、液空間速度1h−1、水素/油比200NL/Lの条件下で、4時間、触媒の予備硫化を行った。
固定床流通式反応装置Bを用い、原料油としてパーム油B(15℃における密度:0.916g/ml、酸素分:11.3質量%、塩素分:7.4質量ppm、よう素価:51.5、含酸素有機化合物に占めるトリグリセライド構造を有する化合物の割合:99.6モル%)を通油し、薬剤注入部よりアンモニアの1質量%の水溶液を0.12g/hで導入し、反応管から薬剤注入部までの温度を300℃とした以外は比較例1と同様にして水素化処理及び回収物の評価を行った。アンモニアの導入量は窒素原子として原料油中の塩素分1gあたり2.91gとなる。回収物を評価した結果、通油した原料油100gあたり水10.2g(回収された水の質量から薬剤注入部より導入された水溶液の質量を差し引いている)、炭化水素油84.1gが生成しており未反応原料油は存在しなかった。また、炭化水素油中の酸素濃度、塩素濃度、窒素濃度及びよう素価はそれぞれ0.1質量ppm以下、0.1質量%以下、0.1質量ppm以下、0.06であった。一方、水中の塩素濃度は72.3質量ppmでありpHは9.8であった。反応開始より4,000時間が経過した時点で反応を終了し、反応管と薬剤注入部の間の配管及びL字型配管の内側を調査した結果、腐食は全く観測されなかった。
固定床流通式反応装置Bを用い、触媒の充填量を300mlとし、薬剤注入部よりジエチルアミンを0.08g/hで導入し、反応管から薬剤注入部までの温度を280℃とした以外は、実施例1と同様にして水素化処理及び回収物の評価を行った。ジエチルアミンの導入量は窒素原子として原料油中の塩素分1gあたり7.64gとなる。回収物を評価した結果、通油した原料油100gあたり水10.3g、炭化水素油84,2gが生成しており未反応原料油は存在しなかった。また、炭化水素油中の酸素濃度、塩素濃度、窒素濃度及びよう素価はそれぞれ0.1質量ppm以下、0.1質量%以下、0.1質量ppm以下、0.06であった。一方、水中の塩素濃度は71.9質量ppmでありpHは11.5であった。反応開始より2,000時間が経過した時点で反応を終了し、反応管と薬剤注入部の間の配管及びL字型配管の内側を調査した結果、腐食は全く観測されなかった。
実施例1におけるアンモニアの1%水溶液の代わりに水酸化ナトリウムの1%水溶液を用いたこと以外は実施例1と同様にして、水素化精製を行った。反応開始より192時間が経過したところで水酸化ナトリウムの水溶液を導入することができなくなった。薬液注入部の配管を調べた結果、固体状の水酸化ナトリウムで閉塞が起こっていた。
Claims (9)
- 水素の存在下、含酸素有機化合物及び非水溶性の含塩素化合物を含有する原料油と、多孔性無機酸化物を含有する担体並びに該担体上に担持された周期律表第VIA族及び第VIII族から選ばれる少なくとも1種以上の金属を含んで構成される水素化触媒と、を接触させて、前記含酸素有機化合物の水素化脱酸素により炭化水素油及び水蒸気の状態の水を生成させるとともに、前記非水溶性の含塩素化合物を水溶性の含塩素化合物に変換する第1の工程と、
前記第1の工程の反応生成物を前記水が水蒸気である状態に保ち、前記第1の工程の反応生成物と、常圧における沸点が100℃以下でありかつ水溶性である含窒素ブレンステッド塩基化合物と、を接触させて被処理物を得る第2の工程と、
前記被処理物を、水蒸気の状態の前記水が液化する温度以下に冷却して、前記水溶性の含塩素化合物及び前記含窒素ブレンステッド塩基化合物を含有する水相を形成させた後、該水相を前記被処理油から分離し、前記炭化水素油を含有する生成油を得る第3の工程と、
を備えることを特徴とする炭化水素油の製造方法。 - 前記原料油の全量を基準として、前記原料油における酸素分の含有量が1〜15質量%であり、前記原料油における塩素分の含有量が0.1〜50質量ppmであることを特徴とする、請求項1に記載の炭化水素油の製造方法。
- 前記第1の工程において、前記原料油中における塩素分1g当たり2〜1200kgの水を副生させることを特徴とする、請求項1又は2に記載の炭化水素油の製造方法。
- 前記第2の工程において、前記原料油中における塩素分1g当たり、窒素原子換算で0.4〜8gとなる含窒素ブレンステッド塩基化合物と前記反応生成物とを接触させることを特徴とする、請求項1〜3のいずれか1項に記載の炭化水素油の製造方法。
- 前記含窒素ブレンステッド塩基化合物がアンモニアであることを特徴とする、請求項1〜4のいずれか1項に記載の炭化水素油の製造方法。
- 前記含酸素有機化合物が動植物由来油脂であり、該動植物由来油脂に占める脂肪酸および/またはエステル体構造を有する化合物の割合が90モル%以上であることを特徴とする、請求項1〜5のいずれか1項に記載の炭化水素油の製造方法。
- 前記多孔性無機酸化物が、アルミニウム、ケイ素、ジルコニウム、ホウ素、チタン、マグネシウムから選ばれる2種以上の元素を含んで構成されていることを特徴とする、請求項1〜6のいずれか1項に記載の炭化水素油の製造方法。
- 前記第1の工程において、水素圧力2〜10MPa、液空間速度0.1〜3.0h−1、水素油比150〜1500NL/L、反応温度150〜380℃の条件下で、前記原料油と前記水素化触媒とを接触させることを特徴とする、請求項1〜7のいずれか1項に記載の炭化水素油の製造方法。
- 前記生成油の全量を基準として、前記生成油における酸素分の含有量が1質量%以下であり、前記生成油における塩素分の含有量が0.1質量ppm以下であり、前記生成油におけるよう素価が0.1以下であることを特徴とする、請求項1〜8のいずれか1項に記載の炭化水素油の製造方法。
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008239791A JP5070169B2 (ja) | 2008-09-18 | 2008-09-18 | 炭化水素油の製造方法 |
PCT/JP2009/066158 WO2010032748A1 (ja) | 2008-09-18 | 2009-09-16 | 炭化水素油の製造方法 |
EP09814593.1A EP2333030A4 (en) | 2008-09-18 | 2009-09-16 | PROCESS FOR PRODUCING HYDROCARBON OIL |
KR1020117006126A KR101595752B1 (ko) | 2008-09-18 | 2009-09-16 | 탄화수소유의 제조방법 |
AU2009293769A AU2009293769B2 (en) | 2008-09-18 | 2009-09-16 | Process for producing hydrocarbon oil |
MYPI20111252 MY152298A (en) | 2008-09-18 | 2009-09-16 | Processfor producing hydrocarbon oil |
BRPI0918863A BRPI0918863A2 (pt) | 2008-09-18 | 2009-09-16 | processo para a produção de óleo de hidrocarboneto |
CN200980136755.1A CN102159681B (zh) | 2008-09-18 | 2009-09-16 | 烃油的制造方法 |
US13/119,310 US8551325B2 (en) | 2008-09-18 | 2009-09-16 | Process for producing hydrocarbon oil |
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JP2008239791A JP5070169B2 (ja) | 2008-09-18 | 2008-09-18 | 炭化水素油の製造方法 |
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JP2010070650A JP2010070650A (ja) | 2010-04-02 |
JP5070169B2 true JP5070169B2 (ja) | 2012-11-07 |
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US (1) | US8551325B2 (ja) |
EP (1) | EP2333030A4 (ja) |
JP (1) | JP5070169B2 (ja) |
KR (1) | KR101595752B1 (ja) |
CN (1) | CN102159681B (ja) |
AU (1) | AU2009293769B2 (ja) |
BR (1) | BRPI0918863A2 (ja) |
MY (1) | MY152298A (ja) |
WO (1) | WO2010032748A1 (ja) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
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US8937202B2 (en) | 2010-02-23 | 2015-01-20 | Battelle Memorial Institute | Processes and systems for the production of propylene glycol from glycerol |
US8366907B2 (en) * | 2010-08-02 | 2013-02-05 | Battelle Memorial Institute | Deoxygenation of fatty acids for preparation of hydrocarbons |
US8669405B2 (en) * | 2011-02-11 | 2014-03-11 | Kior, Inc. | Stable bio-oil |
EP2877557A1 (en) | 2012-07-24 | 2015-06-03 | Reliance Industries Limited | A method for removing chlorides from hydrocarbon stream by steam stripping |
US20160096782A1 (en) * | 2014-10-01 | 2016-04-07 | Uop Llc | Methods and apparatuses for processing bio-derived normal nonane |
CN104371758B (zh) * | 2014-10-29 | 2016-02-24 | 华东师范大学 | 通过油脂与供氢溶剂共活化制备生物航煤的方法 |
JP6642903B2 (ja) * | 2015-03-31 | 2020-02-12 | 三菱重工サーマルシステムズ株式会社 | 冷媒循環装置、冷媒循環方法、冷媒充填方法および冷媒循環装置の運転方法 |
SG10201803633UA (en) | 2018-04-30 | 2019-11-28 | Green Technology Research Co Ltd | Process using bio-based material and the products thereof |
US20220041938A1 (en) * | 2020-08-06 | 2022-02-10 | Chevron U.S.A. Inc. | Upgrading of low value lipid feedstocks for refinery processing |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
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DE2164074C3 (de) * | 1971-12-23 | 1974-10-10 | Bayer Ag, 5090 Leverkusen | Verfahren zum Dehydrochlorieren von Chlorkohlenwasserstoffen |
DE3623430A1 (de) * | 1986-07-11 | 1988-01-28 | Veba Oel Entwicklungs Gmbh | Verfahren zur hydrierenden behandlung von mit chlorbiphenylen u. dgl. kontaminierten mineraloelen |
US4719007A (en) * | 1986-10-30 | 1988-01-12 | Uop Inc. | Process for hydrotreating a hydrocarbonaceous charge stock |
US5951852A (en) * | 1993-12-23 | 1999-09-14 | Commonwealth Scientific And Industrial Research Organisation Et Al. | Destruction of halide containing organics and solvent purification |
JP2000328070A (ja) * | 1999-03-12 | 2000-11-28 | Ube Ind Ltd | 廃棄物ガス化処理方法 |
US7232935B2 (en) * | 2002-09-06 | 2007-06-19 | Fortum Oyj | Process for producing a hydrocarbon component of biological origin |
ES2283736T5 (es) * | 2002-09-06 | 2017-06-09 | Neste Oil Oyj | Procedimiento para producir un componente de hidrocarburo de origen biológico |
JP4567961B2 (ja) | 2003-11-27 | 2010-10-27 | 株式会社レボインターナショナル | 油脂からのデイーゼル燃料油製造プロセス |
JP2005154674A (ja) | 2003-11-28 | 2005-06-16 | Nippon Polyurethane Ind Co Ltd | 水性一液コーティング剤用ポリウレタンエマルジョンの製造方法 |
US8142527B2 (en) * | 2005-03-21 | 2012-03-27 | Ben-Gurion University Of The Negev Research And Development Authority | Production of diesel fuel from vegetable and animal oils |
KR20080021664A (ko) | 2005-06-23 | 2008-03-07 | 쉘 인터내셔날 리써취 마트샤피지 비.브이. | 왁스형 파라핀계 공급원료의 유동점 강하 방법 |
EP1741768B2 (en) * | 2005-07-04 | 2023-04-05 | Neste Oyj | Process for the manufacture of diesel range hydrocarbons |
JP4878824B2 (ja) * | 2005-11-30 | 2012-02-15 | Jx日鉱日石エネルギー株式会社 | 環境低負荷型燃料の製造方法および環境低負荷型燃料 |
EP1960497B1 (en) * | 2005-12-12 | 2020-04-29 | Neste Oyj | Process for producing a saturated hydrocarbon component |
WO2007068796A2 (en) | 2005-12-12 | 2007-06-21 | Neste Oil Oyj | Process for producing a branched hydrocarbon component |
KR20090025241A (ko) | 2006-05-17 | 2009-03-10 | 니폰 오일 코포레이션 (신 니혼 세키유 가부시키 가이샤) | 수소화 처리방법, 환경친화형 가솔린 기재 및 무연 가솔린 조성물 |
JP5196734B2 (ja) | 2006-05-17 | 2013-05-15 | Jx日鉱日石エネルギー株式会社 | 水素化精製方法 |
CN100485016C (zh) * | 2006-10-30 | 2009-05-06 | 华中科技大学 | 利用植物油下脚料炼制生物柴油、磷脂和甘油的方法 |
JP5005451B2 (ja) * | 2007-07-13 | 2012-08-22 | Jx日鉱日石エネルギー株式会社 | 炭化水素油の製造方法 |
US8198492B2 (en) * | 2008-03-17 | 2012-06-12 | Uop Llc | Production of transportation fuel from renewable feedstocks |
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2008
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2009
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- 2009-09-16 AU AU2009293769A patent/AU2009293769B2/en not_active Ceased
- 2009-09-16 MY MYPI20111252 patent/MY152298A/en unknown
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- 2009-09-16 EP EP09814593.1A patent/EP2333030A4/en not_active Withdrawn
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Also Published As
Publication number | Publication date |
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AU2009293769A1 (en) | 2010-03-25 |
CN102159681B (zh) | 2014-04-02 |
MY152298A (en) | 2014-09-15 |
US20110237853A1 (en) | 2011-09-29 |
WO2010032748A1 (ja) | 2010-03-25 |
AU2009293769B2 (en) | 2016-03-03 |
BRPI0918863A2 (pt) | 2015-12-01 |
JP2010070650A (ja) | 2010-04-02 |
US8551325B2 (en) | 2013-10-08 |
EP2333030A1 (en) | 2011-06-15 |
CN102159681A (zh) | 2011-08-17 |
EP2333030A4 (en) | 2015-02-25 |
KR101595752B1 (ko) | 2016-02-19 |
KR20110059851A (ko) | 2011-06-07 |
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