KR980000568A - Impregnated activated carbon for removing sulfide gas and its manufacturing method - Google Patents

Impregnated activated carbon for removing sulfide gas and its manufacturing method Download PDF

Info

Publication number
KR980000568A
KR980000568A KR1019980001645A KR19980001645A KR980000568A KR 980000568 A KR980000568 A KR 980000568A KR 1019980001645 A KR1019980001645 A KR 1019980001645A KR 19980001645 A KR19980001645 A KR 19980001645A KR 980000568 A KR980000568 A KR 980000568A
Authority
KR
South Korea
Prior art keywords
activated carbon
mercaptan
impregnated
sulfide
alkali metal
Prior art date
Application number
KR1019980001645A
Other languages
Korean (ko)
Other versions
KR100235113B1 (en
Inventor
박종학
성준식
Original Assignee
정영무
주식회사 삼천리
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 정영무, 주식회사 삼천리 filed Critical 정영무
Priority to KR1019980001645A priority Critical patent/KR100235113B1/en
Publication of KR980000568A publication Critical patent/KR980000568A/en
Application granted granted Critical
Publication of KR100235113B1 publication Critical patent/KR100235113B1/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/20Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising free carbon; comprising carbon obtained by carbonising processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/28Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
    • B01J20/28054Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their surface properties or porosity
    • B01J20/28057Surface area, e.g. B.E.T specific surface area
    • B01J20/28066Surface area, e.g. B.E.T specific surface area being more than 1000 m2/g
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/28Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
    • B01J20/28054Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their surface properties or porosity
    • B01J20/28078Pore diameter
    • B01J20/28083Pore diameter being in the range 2-50 nm, i.e. mesopores
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/30Processes for preparing, regenerating, or reactivating
    • B01J20/32Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
    • B01J20/3231Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
    • B01J20/3234Inorganic material layers
    • B01J20/3236Inorganic material layers containing metal, other than zeolites, e.g. oxides, hydroxides, sulphides or salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L3/00Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
    • C10L3/06Natural gas; Synthetic natural gas obtained by processes not covered by C10G, C10K3/02 or C10K3/04
    • C10L3/10Working-up natural gas or synthetic natural gas
    • C10L3/101Removal of contaminants

Abstract

본 발명은 C3이하의 연료용 가스혼합물에서 부취제로 혼합된 황화물 가스를 제거하는데 사용되는 첨착활성탄 및 이의 제조방법에 관한 것으로 알카리 금속수산화물, 염기성 알카리 금속염 또는 구리 또는 철 등의 산화물 또는 염화물의 용액 또는 분산액에 미세공 50%이상 비표면적 800㎡/g이상을 갖는 활성탄을 함침, 건조시켜 제조하며 황화물 가스를 제거하는데 우수한 효율을 발휘하여 이동성 배출가스 수집장비에 사용되기 적합하다.The present invention relates to an impregnated activated carbon used to remove sulfide gas mixed as a odorant in a gas mixture for fuels of C 3 or less, and a method for preparing the same, and a solution of an oxide or chloride such as alkali metal hydroxide, basic alkali metal salt or copper or iron. Alternatively, the dispersion is prepared by impregnating and drying activated carbon having a specific surface area of 800 m 2 / g or more with a fine pore size of 50% or more, and exhibits excellent efficiency in removing sulfide gas, and is suitable for use in mobile exhaust gas collection equipment.

Description

황화물 가스를 게거하기 위한 첨착활성탄 및 이의 제조방법Impregnated activated carbon for removing sulfide gas and its manufacturing method

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

제1도는 본 발명의 첨착활성탄 제조장치의 공정설명도이다.1 is a process explanatory diagram of the impregnated activated carbon production apparatus of the present invention.

Claims (15)

직경 20A이하의 마이크로 기공이 50%이상이고, 평균 세공직경이 13∼12A, 비표면적 800㎡/g이상이며 입자경이 본질적으로 4×8메쉬인 활성탄소를 1∼30% 농도의 알칼리 금속 수산화물, 염기성 알칼리 금속염, 철 또는 구리 산화물 또는 염화물과 아연산화물로 이루어진 군에서 택일된 화합물 용액 또는 분산액으로 함침 및 건조시킨, 본질적으로 C3이하의 가스 혼합물에서 황화물 가스를 제거하는데 사용되는 침착활성탄.Alkali metal hydroxides having 1 to 30% concentration of activated carbon having a micropore diameter of 20 A or less and 50% or more, an average pore diameter of 13 to 12 A, a specific surface area of 800 m 2 / g or more, and a particle diameter of 4 × 8 mesh. A deposited activated carbon used to remove sulfide gas from an essentially C 3 or less gas mixture impregnated and dried with an alternative compound solution or dispersion from the group consisting of basic alkali metal salts, iron or copper oxides or chlorides and zinc oxides. 제1항에 있어서, 상기 마이크로 가공이 70%이상이고, 평균세공반경이 13∼20A, 비표면적인 1000㎡/g이상이고, 입자경이 본질적으로 4×6메쉬인 활성탄소를 함침 및 건조시킨 첨착활성탄.The impregnated and dried impregnated activated carbon according to claim 1, wherein the micromachining is 70% or more, the average pore radius is 13-20 A, the specific surface area is 1000 m 2 / g or more, and the particle size is essentially 4 × 6 mesh. Activated carbon. 제1항에 있어서, 상기 C3이하의 가스혼합물이 LNG인 첨착활성탄.The impregnated activated carbon according to claim 1, wherein the gas mixture of C 3 or less is LNG. 제1항에 있어서, 상기 황화물 가스가 메르캅탄, 설파이드 및 이황화수소로 이루어진 군에서 택일된 첨착활성탄.The impregnated activated carbon of claim 1, wherein the sulfide gas is selected from the group consisting of mercaptan, sulfide, and hydrogen disulfide. 제2항 또는 제3항에 있어서, 상기 함침 화합물이 알칼리 금속 수산화물, 알칼리 금속 탄산염, 철과 구리 염화물 및 산화물과 아연산화물로 이루어진 군에서 택일된 첨착활성탄.The impregnated activated carbon according to claim 2 or 3, wherein the impregnating compound is selected from the group consisting of alkali metal hydroxides, alkali metal carbonates, iron and copper chlorides, and oxides and zinc oxides. 제5항에 있어서, 상기 황화물 가스가 메틸 메르캅탄, 에틸 메르캅탄, 터시어리부틸 메르캅탄, 이소프로필 메르캅탄, 노멀프로필 메르캅탄 또는 2급부틸 메르캅탄, 테트라 하이드로 티오펜, 디에틸 설파이드, 메틸에틸 설파이드, 디메틸 설파이드 디에틸 설파이드 또는 이황화수소인 첨착활성탄.The method of claim 5, wherein the sulfide gas is methyl mercaptan, ethyl mercaptan, tertiary butyl mercaptan, isopropyl mercaptan, normal propyl mercaptan or secondary butyl mercaptan, tetra hydrothiophene, diethyl sulfide, methyl Impregnated activated carbon which is ethyl sulfide, dimethyl sulfide diethyl sulfide or hydrogen disulfide. 직경 20A이하의 마이크로 기공이 50%이상이고, 평균 세공직경이 10∼25A, 비표면적 800㎡/g이상이며 입자경이 본질적으로 4×8메쉬인 활성탄소를 준비하는 단계; 상기 활성탄소를 1∼30%농도의 알칼리 금속 수산화물, 염기성 알칼리 금속염, 철 또는 구리산화물 또는 염화물과 아연 산화물로 이루어진 군에서 택일된 화합물 용액 또는 분산액에 침지하여 에어레이숀 교반하는 단계; 상기 침지된 활성탄을 건조하는 단계를 포함하고, 상기 에어레이숀 교반 단계에서 발생되는 미분활성탄을 여과하여 제거하는, 본질적으로 C3이하의 연료용 가스 혼합물에서 황화물 가스를 제거하는데 사용되는 첨착활성탄의 제조방법.Preparing activated carbon having a micropore of 20 A or less in diameter of 50% or more, an average pore diameter of 10 to 25 A, a specific surface area of 800 m 2 / g or more, and a particle diameter of 4 × 8 mesh; Immersing the activated carbon in a compound solution or dispersion selected from the group consisting of alkali metal hydroxides, basic alkali metal salts, iron or copper oxides, chlorides and zinc oxides at a concentration of 1 to 30%, followed by aeration with air suspension; Drying of the impregnated activated carbon, wherein the activated activated carbon used to remove sulfide gas is essentially removed from the gas mixture for fuel of C 3 or lower, which is filtered off to remove the fine activated carbon generated in the air-action stirring step. Manufacturing method. 제7항에 있어서, 상기 마이크로 기공이 70%이상이고, 평균세공반경이 13-20A, 비표면적인 1000㎡/g이상이고, 입자경이 본질적으로 4×6메쉬인 활성탄소를 함침 및 건조시킨 첨착활성탄의 제조방법.The impregnated and dried impregnated activated carbon according to claim 7, wherein the micropores are 70% or more, the average pore radius is 13-20 A, the specific surface area is 1000 m 2 / g or more, and the particle size is essentially 4 × 6 mesh. Method for producing activated carbon. 제7항에 있어서, 상기 C3이하의 가스혼합물이 LNG인 침착활성탄의 제조방법.The method of claim 7, wherein the gas mixture of C 3 or less is LNG. 제7항 또는 제8항에 있어서, 상기 함침화합물이 알칼리 금속 수산화물, 알칼리 금속 탄산염, 철과 구리 염화물 및 산화물과 아연산화물로 이루어진 군에서 택일된 첨착활성탄의 제조방법.The method for producing impregnated activated carbon according to claim 7 or 8, wherein the impregnating compound is selected from the group consisting of alkali metal hydroxides, alkali metal carbonates, iron and copper chlorides, and oxides and zinc oxides. 제7항에 있어서, 상기 황화물 가스가 메틸 메르캅탄, 에틸 메르캅탄, 터시어리부틸 메르캅탄, 이소프로필 메르캅탄, 노멀프로필 메르캅탄 또는 2급부틸 메르캅탄, 테트라 하이드로 티오펜, 디에틸 설파이드, 메틸에틸 설파이드, 디메틸 설파이드, 디에틸 설파이드 또는 이황화수소인 첨착활성탄의 제조방법.The method of claim 7, wherein the sulfide gas is methyl mercaptan, ethyl mercaptan, tertiarybutyl mercaptan, isopropyl mercaptan, normal propyl mercaptan or secondary butyl mercaptan, tetra hydrothiophene, diethyl sulfide, methyl A process for producing impregnated activated carbon, which is ethyl sulfide, dimethyl sulfide, diethyl sulfide or hydrogen disulfide. 직경 20A이하의 마이크로 기공이 50%이상이고, 평균 세공반경이 10∼25A, 비표면적이 800㎡/g이상이며 입자경이 본질적으로 4×8메쉬인 활성탄을 1-30%농도의 염기성 알칼리 금속염으로 함침 건조된 첨착활성탄 10 내지 50중량%와 상기 활성탄을 1-30%농도의 철 또는 구리 염화물로 함침 건조된 첨착활성탄 50 내지 90중량%로 구성되는 본질적으로 C3이하의 연료용 가스에서 황화물 가스를 제거하는데 사용되는 첨착활성탄 혼합물.Activated carbon with a micropore diameter of 20 A or less and 50% or more, an average pore radius of 10 to 25 A, a specific surface area of 800 m 2 / g or more and a particle diameter of 4 × 8 mesh essentially as a basic alkali metal salt having a concentration of 1-30% Sulphide gas in essentially C 3 or less fuel gas consisting of 10 to 50% by weight of impregnated dried activated carbon and 50 to 90% by weight of impregnated activated carbon impregnated with 1-30% of iron or copper chloride. Impregnated activated carbon mixtures used to remove. 제12항에 있어서, 상기 마이크로 기공이 70%이상이고, 평균세공반경이 13-20A, 비표면적인 1000㎡/g이상이고, 입자경이 본질적으로 4×6메쉬인 활성탄소를 함침 및 건조시킨 첨착활성탄 혼합물.The impregnated and dried impregnated activated carbon according to claim 12, wherein the micropores are 70% or more, the average pore radius is 13-20 A, the specific surface area is 1000 m 2 / g or more, and the particle diameter is essentially 4 × 6 mesh. Activated carbon mixture. 제12항에 있어서, 상기 C3이하의 가스혼합물이 LNG인 첨착활성탄 혼합물.13. The impregnated activated carbon mixture according to claim 12, wherein the gas mixture of C 3 or less is LNG. 제12항에 있어서, 상기 황화물 가스가 메틸 메르캅탄, 에틸 메르캅탄, 터시어리부틸 메르캅탄, 이소프로필 메르캅탄, 노멀프로필 메르캅탄 또는 2급부틸 메르캅탄, 테트라 하이드로 티오펜, 디에틸 설파이드, 메틸에틸 설파이드, 디메틸 설파이드, 디에틸 설파이드 또는 이황화수소인 첨착활성탄 혼합물.The method of claim 12, wherein the sulfide gas is methyl mercaptan, ethyl mercaptan, tertiarybutyl mercaptan, isopropyl mercaptan, normal propyl mercaptan or secondary butyl mercaptan, tetra hydrothiophene, diethyl sulfide, methyl Impregnated activated carbon mixtures which are ethyl sulfide, dimethyl sulfide, diethyl sulfide or hydrogen disulfide. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019980001645A 1998-01-21 1998-01-21 Incorporated active carbon for removing sulfide gas and preparation method thereof KR100235113B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019980001645A KR100235113B1 (en) 1998-01-21 1998-01-21 Incorporated active carbon for removing sulfide gas and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019980001645A KR100235113B1 (en) 1998-01-21 1998-01-21 Incorporated active carbon for removing sulfide gas and preparation method thereof

Publications (2)

Publication Number Publication Date
KR980000568A true KR980000568A (en) 1998-03-30
KR100235113B1 KR100235113B1 (en) 1999-12-15

Family

ID=19531855

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019980001645A KR100235113B1 (en) 1998-01-21 1998-01-21 Incorporated active carbon for removing sulfide gas and preparation method thereof

Country Status (1)

Country Link
KR (1) KR100235113B1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100426962B1 (en) * 2001-03-13 2004-04-13 황수덕 A Impregnated Adsorbent to remove Hydrogen Sulfide Gas and a Preparation Method of the Same
KR100558895B1 (en) * 2004-08-05 2006-03-10 한국항공우주연구원 Adsorbents for organic sulfur compounds, Method for manufacturing them and Method for desulfurizing of town gas using them
KR100704929B1 (en) * 2006-03-16 2007-04-09 (주)선진환경 Fe(iii)-impregnated activated carbon for removing heavy metal ions and organic matter by adsorption, and the manufacturing method of the the same
KR102572868B1 (en) 2022-09-20 2023-08-31 한국건설기술연구원 Method for manufacturing activated carbon impreganated with iron component, and method for removing synthetic organic chemicals in aqua using the same

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100855772B1 (en) * 2006-11-21 2008-09-01 주식회사 삼천리 Adsorbent to adsorb the sulfurour gas contained in fuel gas, and desulfurization equipement in fuel cell system using such adsorbent
KR102054289B1 (en) * 2012-03-16 2019-12-10 웅진코웨이 주식회사 Filter impregnated alkali metal compound for removing NO2 and air purifier including thereof
JP7294755B2 (en) * 2016-11-03 2023-06-20 コロンバス・インダストリーズ・インコーポレイテッド Surface-modified carbon and adsorbents for improved efficiency in removing gaseous pollutants
KR102145394B1 (en) 2020-03-23 2020-08-19 한소 주식회사 High performance spray-impregnated activated carbon impregnated with various metal salts and method for manufacturing the same
KR102653377B1 (en) * 2023-03-22 2024-04-02 주식회사 지티사이언 Manufacturing method of chemical adsorbent for removing harmful gas and the apparatus thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100426962B1 (en) * 2001-03-13 2004-04-13 황수덕 A Impregnated Adsorbent to remove Hydrogen Sulfide Gas and a Preparation Method of the Same
KR100558895B1 (en) * 2004-08-05 2006-03-10 한국항공우주연구원 Adsorbents for organic sulfur compounds, Method for manufacturing them and Method for desulfurizing of town gas using them
KR100704929B1 (en) * 2006-03-16 2007-04-09 (주)선진환경 Fe(iii)-impregnated activated carbon for removing heavy metal ions and organic matter by adsorption, and the manufacturing method of the the same
KR102572868B1 (en) 2022-09-20 2023-08-31 한국건설기술연구원 Method for manufacturing activated carbon impreganated with iron component, and method for removing synthetic organic chemicals in aqua using the same

Also Published As

Publication number Publication date
KR100235113B1 (en) 1999-12-15

Similar Documents

Publication Publication Date Title
EP3068531B1 (en) Sulfidized sorbent composition for the removal of sulfur compounds from a gas stream
CA2052269C (en) Sorption of trialkyl arsines
KR980000568A (en) Impregnated activated carbon for removing sulfide gas and its manufacturing method
HRP20020945A2 (en) Desulfurization and sorbents for same
GB2106010A (en) Filter
CA2481527A1 (en) Desulfurization and sorbents for same
ATE288789T1 (en) CATALYST AND METHOD FOR PURIFYING MATERIAL STREAMS
ES2150221T3 (en) CATALYST THAT IS USED TO SELECTIVELY OXIDIZE COMPOUNDS OF ELEMENTAL SULFUR, PROCEDURE FOR PREPARING SUCH CATALYST AND PROCEDURE FOR CARRYING OUT SUCH OXIDATION.
CN108686673B (en) Ozone catalytic oxidation catalyst and preparation method thereof
ATE254962T1 (en) METAL-CONTAINING MACROSTRUCTURES OF POROUS INORGANIC PARTICLES, THEIR PRODUCTION AND APPLICATION
DE50006954D1 (en) Stable, platelet-shaped, calcitic calcium carbonate, process for its production and its use
CN104190242B (en) A kind of hydrogen sulfide scavenging material and preparation method thereof
CN108993504B (en) Modified activated coke for demercuration of sulfur-containing flue gas and preparation method thereof
RU99100622A (en) METHOD FOR PRELIMINARY SULPHATION OF HYDROCARBON TRANSFORMATION CATALYSTS, PRELIMINARY SULPHATED CATALYST AND METHOD FOR TURNING HYDROCARBON RAW MATERIALS
CA2229340A1 (en) Novel photocatalyst, preparation therefor and method for producing hydrogen using the same
KR100506813B1 (en) Mn oxide catalyst for decomposing ozone and the method therefor
EP1142635B1 (en) Supported deodorizing catalysts and preparation thereof
JPS6322184B2 (en)
CN109908951B (en) Multi-stage micro-mesoporous low-temperature catalyst and preparation method thereof
KR20100048948A (en) A sorbent composition, the preparation method thereof, and the process for removing sulfur oxides and nitrogen oxides in a flue gas by the sorbent composition
Li et al. Preparation, characterization of sludge adsorbent and investigations on its removal of hydrogen sulfide under room temperature
CN115138329B (en) Novel H2Nb4O11 nanotube desulfurization adsorbent and preparation method thereof
MXPA97006185A (en) Process to reactivate sorbents off
CN115634712B (en) Preparation method of CVOCs catalytic oxidation double-acid-site catalyst
RU2050188C1 (en) Method for production of catalyst for removal of oxygen from hydrogen sulfide-containing gases

Legal Events

Date Code Title Description
A201 Request for examination
G15R Request for early opening
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20120917

Year of fee payment: 14

FPAY Annual fee payment

Payment date: 20130917

Year of fee payment: 15

FPAY Annual fee payment

Payment date: 20141021

Year of fee payment: 16

FPAY Annual fee payment

Payment date: 20150917

Year of fee payment: 17

FPAY Annual fee payment

Payment date: 20160921

Year of fee payment: 18

FPAY Annual fee payment

Payment date: 20170921

Year of fee payment: 19

EXPY Expiration of term