DE2653863C2 - - Google Patents

Info

Publication number
DE2653863C2
DE2653863C2 DE2653863A DE2653863A DE2653863C2 DE 2653863 C2 DE2653863 C2 DE 2653863C2 DE 2653863 A DE2653863 A DE 2653863A DE 2653863 A DE2653863 A DE 2653863A DE 2653863 C2 DE2653863 C2 DE 2653863C2
Authority
DE
Germany
Prior art keywords
catalyst
molybdate
potassium
bismuth
water
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
Application number
DE2653863A
Other languages
German (de)
English (en)
Other versions
DE2653863A1 (de
Inventor
Tao Ping Chesterfield Mo. Us Li
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monsanto Co
Original Assignee
Monsanto Co
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 Monsanto Co filed Critical Monsanto Co
Publication of DE2653863A1 publication Critical patent/DE2653863A1/de
Application granted granted Critical
Publication of DE2653863C2 publication Critical patent/DE2653863C2/de
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/24Preparation of carboxylic acid nitriles by ammoxidation of hydrocarbons or substituted hydrocarbons
    • C07C253/26Preparation of carboxylic acid nitriles by ammoxidation of hydrocarbons or substituted hydrocarbons containing carbon-to-carbon multiple bonds, e.g. unsaturated aldehydes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/85Chromium, molybdenum or tungsten
    • B01J23/88Molybdenum
    • B01J23/887Molybdenum containing in addition other metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/8876Arsenic, antimony or bismuth
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/14Phosphorus; Compounds thereof
    • B01J27/186Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J27/188Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
    • B01J27/19Molybdenum
    • B01J27/192Molybdenum with bismuth
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/33Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
    • C07C45/34Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/33Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
    • C07C45/34Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
    • C07C45/35Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds in propene or isobutene
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/25Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/25Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
    • C07C51/252Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring of propene, butenes, acrolein or methacrolein
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2523/00Constitutive chemical elements of heterogeneous catalysts
    • 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
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/52Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
DE19762653863 1975-11-28 1976-11-26 Verfahren zur herstellung von katalysatoren fuer die ammonoxydation Granted DE2653863A1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US05/636,011 US4040978A (en) 1975-11-28 1975-11-28 Production of (amm)oxidation catalyst

Publications (2)

Publication Number Publication Date
DE2653863A1 DE2653863A1 (de) 1977-06-08
DE2653863C2 true DE2653863C2 (US20030227983A1-20031211-M00013.png) 1988-10-20

Family

ID=24550038

Family Applications (1)

Application Number Title Priority Date Filing Date
DE19762653863 Granted DE2653863A1 (de) 1975-11-28 1976-11-26 Verfahren zur herstellung von katalysatoren fuer die ammonoxydation

Country Status (14)

Country Link
US (1) US4040978A (US20030227983A1-20031211-M00013.png)
JP (1) JPS6029536B2 (US20030227983A1-20031211-M00013.png)
AU (1) AU502608B2 (US20030227983A1-20031211-M00013.png)
BE (1) BE848793A (US20030227983A1-20031211-M00013.png)
BR (1) BR7607932A (US20030227983A1-20031211-M00013.png)
CA (1) CA1082165A (US20030227983A1-20031211-M00013.png)
DE (1) DE2653863A1 (US20030227983A1-20031211-M00013.png)
DK (1) DK535276A (US20030227983A1-20031211-M00013.png)
ES (1) ES453604A1 (US20030227983A1-20031211-M00013.png)
FR (1) FR2332803A1 (US20030227983A1-20031211-M00013.png)
GB (1) GB1564545A (US20030227983A1-20031211-M00013.png)
IL (1) IL50998A (US20030227983A1-20031211-M00013.png)
IT (1) IT1107704B (US20030227983A1-20031211-M00013.png)
NL (1) NL7613086A (US20030227983A1-20031211-M00013.png)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4168246A (en) * 1975-11-28 1979-09-18 Monsanto Company Production of (amm)oxidation catalyst
US4148757A (en) * 1977-08-10 1979-04-10 The Standard Oil Company Process for forming multi-component oxide complex catalysts
US4212766A (en) * 1978-04-21 1980-07-15 Standard Oil Company Process for forming multi-component oxide complex catalysts
JPS5538330A (en) * 1978-09-13 1980-03-17 Ube Ind Ltd Preparation of acrylonitrile
US4224187A (en) * 1978-11-13 1980-09-23 Celanese Corporation Olefin oxidation catalyst and process for its preparation
DE2849715A1 (de) * 1978-11-16 1980-05-29 Hoechst Ag Traegerkatalysator und verfahren zu seiner herstellung
US4405498A (en) * 1979-12-17 1983-09-20 Monsanto Company Oxidation and ammoxidation catalysts
EP0061830B1 (en) * 1981-02-17 1984-08-29 The Standard Oil Company Preparation of composite oxidation catalyst and use thereof for the production of unsaturated aldehydes and acids from propylene and isobutylene
US4388223A (en) * 1981-04-06 1983-06-14 Euteco Impianti S.P.A. Catalyst for the conversion of unsaturated hydrocarbons into diolefins or unsaturated aldehydes and nitriles, and process for preparing the same
US4415482A (en) * 1981-11-12 1983-11-15 Monsanto Company Oxidation and ammoxidation catalyst
JPH01131336U (US20030227983A1-20031211-M00013.png) * 1988-03-01 1989-09-06
JP2520279B2 (ja) * 1988-03-03 1996-07-31 日東化学工業株式会社 アクリロニトリルの製造方法
JP2520282B2 (ja) * 1988-04-15 1996-07-31 日東化学工業株式会社 アクリロニトリルの製造方法
FR2670686B1 (fr) * 1990-12-20 1994-08-12 Rhone Poulenc Chimie Composition catalytique pour la preparation d'aldehydes alpha,beta-insatures par oxydation d'olefines en phase gazeuse et procede d'oxydation.
FR2670685B1 (fr) * 1990-12-20 1995-03-10 Rhone Poulenc Chimie Procede de preparation de catalyseurs enrobes a base de molybdates de bismuth et de fer dopes par du phosphore et du potassium.
DE19517106C2 (de) * 1995-05-10 1997-11-06 Doerfert Hans Joachim Sicherheitssystem für mit gefährlichen Stoffen kontaminierte Luft für einen Arbeitsraum einer Abzugwerkbank
US5840648A (en) * 1997-09-02 1998-11-24 The Standard Oil Company Catalyst for the manufacture of acrylonitrile and hydrogen cyanide
US6037304A (en) * 1999-01-11 2000-03-14 Saudi Basic Industries Corporation Highly active and selective catalysts for the production of unsaturated nitriles, methods of making and using the same
US6017846A (en) * 1999-01-11 2000-01-25 Saudi Basic Industries Corporation Highly active and selective catalysts for the production of unsaturated nitriles, methods of making and using the same
US6486091B1 (en) 2000-03-14 2002-11-26 Saudi Basic Industries Corporation Process for making highly active and selective catalysts for the production of unsaturated nitriles
US7649111B2 (en) 2005-07-25 2010-01-19 Saudi Basic Industries Corporation Catalyst for the oxidation of a mixed aldehyde feedstock to methacrylic acid and methods for making and using same
US7732367B2 (en) 2005-07-25 2010-06-08 Saudi Basic Industries Corporation Catalyst for methacrolein oxidation and method for making and using same
US7851397B2 (en) 2005-07-25 2010-12-14 Saudi Basic Industries Corporation Catalyst for methacrolein oxidation and method for making and using same
US7649112B2 (en) 2005-07-25 2010-01-19 Saudi Basic Industries Corporation Integrated plant for producing 2-ethyl-hexanol and methacrylic acid and a method based thereon
KR101086731B1 (ko) * 2008-10-17 2011-11-25 금호석유화학 주식회사 1-부텐의 산화/탈수소화 반응에서 1,3-부타디엔 제조용 비스무스 몰리브덴 철 복합 산화물 촉매 및 제조방법
EP2550097B1 (en) 2010-03-23 2020-11-11 INEOS Europe AG High efficiency ammoxidation process and mixed metal oxide catalysts
US8455388B2 (en) 2010-03-23 2013-06-04 Ineos Usa Llc Attrition resistant mixed metal oxide ammoxidation catalysts
US8153546B2 (en) 2010-03-23 2012-04-10 Ineos Usa Llc Mixed metal oxide ammoxidation catalysts
US8420566B2 (en) * 2010-03-23 2013-04-16 Ineos Usa Llc High efficiency ammoxidation process and mixed metal oxide catalysts
US8258073B2 (en) * 2010-03-23 2012-09-04 Ineos Usa Llc Process for preparing improved mixed metal oxide ammoxidation catalysts
US9433929B2 (en) * 2011-09-21 2016-09-06 Ineos Europe Ag Mixed metal oxide catalysts
US8921257B2 (en) 2011-12-02 2014-12-30 Saudi Basic Industries Corporation Dual function partial oxidation catalyst for propane to acrylic acid conversion
DE102012010542A1 (de) 2011-12-20 2013-06-20 CCP Technology GmbH Verfahren und anlage zur erzeugung von synthesegas
US8722940B2 (en) 2012-03-01 2014-05-13 Saudi Basic Industries Corporation High molybdenum mixed metal oxide catalysts for the production of unsaturated aldehydes from olefins
WO2015183283A1 (en) 2014-05-29 2015-12-03 Ineos Usa, Llc Improved selective ammoxidation catalysts
KR101974709B1 (ko) 2014-05-29 2019-05-02 이네오스 유럽 아게 개선된 선택적 가암모니아산화 촉매
US9844769B2 (en) 2014-12-17 2017-12-19 Ineos Europe Ag Mixed metal oxide ammoxidation catalysts
US9815045B2 (en) 2015-03-23 2017-11-14 Clariant Corporation Metal oxide catalyst material and processes for making and using same
JP6905531B2 (ja) 2016-01-09 2021-07-21 アセンド・パフォーマンス・マテリアルズ・オペレーションズ・リミテッド・ライアビリティ・カンパニーAscend Performance Materials Operations Llc アクリロニトリル反応器供給物流れでのシアン化水素の直接生成のための触媒組成物および方法
US10626082B2 (en) 2016-10-11 2020-04-21 Ineos Europe Ag Ammoxidation catalyst with selective co-product HCN production
US10479760B2 (en) 2017-02-08 2019-11-19 Clariant Corporation Synthetic methods for the preparation of propylene ammoxidation catalysts
US10479759B2 (en) 2017-02-08 2019-11-19 Clariant Corporation Synthetic methods for the preparation of propylene ammoxidation catalysts
JP7101310B2 (ja) * 2019-04-15 2022-07-14 旭化成株式会社 触媒、触媒の製造方法、アクリロニトリルの製造方法
WO2022108323A1 (ko) * 2020-11-17 2022-05-27 주식회사 엘지화학 암모산화 촉매 및 이의 제조 방법과, 상기 암모산화 촉매를 사용한 아크릴로니트릴의 제조 방법

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR79628E (fr) * 1958-10-28 1962-12-28 Montecatini Societa Gen Per L Catalyseur pour la production de formaldéhyde à partir du méthanol
NL298115A (US20030227983A1-20031211-M00013.png) * 1962-09-20
US3471556A (en) * 1964-12-07 1969-10-07 Nippon Kayaku Kk Production of unsaturated aliphatic acids
US3624146A (en) * 1965-08-25 1971-11-30 Grace W R & Co Process for the production of acrylic acid from propylene
US3642930A (en) * 1968-12-30 1972-02-15 Standard Oil Co Ohio Process for the manufacture of isoprene from isoamylenes and methyl butanols and catalyst therefor
US3636066A (en) * 1969-03-05 1972-01-18 Ube Industries Process for the manufacture of acrylonitrile by ammoxidation
BE749305A (fr) * 1969-05-02 1970-10-01 Nippon Kayaku Kk Catalyseur d'oxydation et son utilisation (
JPS4843096B1 (US20030227983A1-20031211-M00013.png) * 1970-01-31 1973-12-17
JPS529649B1 (US20030227983A1-20031211-M00013.png) * 1970-06-12 1977-03-17
US3746657A (en) * 1971-06-28 1973-07-17 Standard Oil Co Catalyst manufacturing process
US3883573A (en) * 1973-06-15 1975-05-13 Standard Oil Co Commercial fixed-bed acrylonitrile or methacrylonitrile

Also Published As

Publication number Publication date
IT1107704B (it) 1985-11-25
JPS6029536B2 (ja) 1985-07-11
BR7607932A (pt) 1977-11-08
JPS5268094A (en) 1977-06-06
DE2653863A1 (de) 1977-06-08
IL50998A0 (en) 1977-01-31
GB1564545A (en) 1980-04-10
BE848793A (fr) 1977-05-26
DK535276A (da) 1977-05-29
AU2002676A (en) 1978-06-01
AU502608B2 (en) 1979-08-02
IL50998A (en) 1980-10-26
FR2332803B1 (US20030227983A1-20031211-M00013.png) 1982-01-15
ES453604A1 (es) 1977-11-16
US4040978A (en) 1977-08-09
CA1082165A (en) 1980-07-22
NL7613086A (nl) 1977-06-01
FR2332803A1 (fr) 1977-06-24

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Representative=s name: BERG, W., DIPL.-CHEM. DR.RER.NAT., PAT.-ANW., 8000

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Representative=s name: TER MEER, N., DIPL.-CHEM. DR.RER.NAT. MUELLER, F.,

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