SU506302A3 - The method of producing liquefied petroleum gas - Google Patents

The method of producing liquefied petroleum gas

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Publication number
SU506302A3
SU506302A3 SU1812197A SU1812197A SU506302A3 SU 506302 A3 SU506302 A3 SU 506302A3 SU 1812197 A SU1812197 A SU 1812197A SU 1812197 A SU1812197 A SU 1812197A SU 506302 A3 SU506302 A3 SU 506302A3
Authority
SU
USSR - Soviet Union
Prior art keywords
petroleum gas
liquefied petroleum
producing liquefied
bbl
hydrocracking
Prior art date
Application number
SU1812197A
Other languages
Russian (ru)
Inventor
Генри Уоткинс Чарльз
Original Assignee
Юниверсал Ойл Продактс Компани (Фирма)
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 Юниверсал Ойл Продактс Компани (Фирма) filed Critical Юниверсал Ойл Продактс Компани (Фирма)
Application granted granted Critical
Publication of SU506302A3 publication Critical patent/SU506302A3/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G65/00Treatment of hydrocarbon oils by two or more hydrotreatment processes only
    • C10G65/02Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only
    • C10G65/10Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including only cracking steps
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G2400/00Products obtained by processes covered by groups C10G9/00 - C10G69/14
    • C10G2400/28Propane and butane

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Description

городные металлы VIII труппы содержатс  в количества 0,01-2 isec. %.City metals of Group VIII are contained in an amount of 0.01-2 isec. %

.Процесс гидрокрекинга провод т при 343-510° С. Наиболее оптима.тьной  вл етс  температура 351-483° С. Давление в зоне реак1ции гидрокрекинга 70,3-175,8 кг/сж, скорость 1подачи углеводородов 0,25-5 единиц объемной часовой скорости жидкости. Концентраци  водорода м /баррель. В качестве Катализатора гидрокрекинга используют один ИЛИ несколько металлов IVB и VII групп Периодической системы элементов, например олово, германий, .нанесейных на кремнезем , .содержащий 12-30 вес. % глинозема.The hydrocracking process is carried out at 343-510 ° C. The most optimal temperature is 351-483 ° C. The pressure in the hydrocracking reaction zone is 70.3-175.8 kg / ss, the rate of hydrocarbon delivery is 0.25-5 units volumetric hourly velocity of the fluid. Hydrogen concentration m / bbl. As a hydrocracking catalyst, one OR several metals of the IVB and VII groups of the Periodic Table of the elements are used, for example, tin, germanium, nonscore on silica, containing 12-30 wt. % alumina.

На второй стадии гидрокреки-нга может быть .применен катализатор, в котором металлические ком поненты прап-итывают кристаллические алюмосиликатные молекул рные сита. В качест1ве молекул рного сита могут быть использованы морденит, .молекул рные сита типа X и Y, а также цеолитсодержащий материал, диспергированный в аморфной матрице глинозема, крем.незема или алюмосиликата .In the second hydrocrack stage, a catalyst may be used in which the metallic components pore crystalline aluminosilicate molecular sieves. Mordenite, molecular sieves of types X and Y, as well as zeolite-containing material dispersed in an amorphous alumina matrix, silica gel or aluminosilicate can be used as molecular sieves.

Реакции гидрокрекинга Я|вл ютс  в основном экзотермически.ми реакци ми. При прохождении сырь  и водорода через слой катал .изатора на1блю1даетс  повышение тэмпе-ратуры . Поэтому во избежание очень сильного повышени  температуры в зонах гидрокрекинга IB одном или нескольких пунктах этих зон 1подают охлаждающий IHOTOK жидкости или газов.Hydrocracking reactions I | are mainly exothermic reactions. With the passage of raw materials and hydrogen through the bed of the catalyst, an increase in temperature is observed. Therefore, in order to avoid a very high temperature increase in the hydrocracking zones IB, one or several points of these zones 1 supply cooling IHOTOK liquids or gases.

Пример I. Получение сжиженного нефт ного газа из т желого углеводородного сырь  с концом кипени  547° С.Example I. Production of liquefied petroleum gas from heavy hydrocarbon feedstock with a boiling point of 547 ° C.

На чертеже .изображена схема установки дл  .реализаЦИИ этого процесса.In the drawing. Depicts the setup diagram for the implementation of this process.

ХараКтбристика сырь :Characteristics of raw materials:

Плотность, ,8756 Пнтервал перегонки, °С: Начальна  точ:ка кипени 210 1.0%338 30%360 50%377 70%398 90%448 Конечна  .ка килени 549 Сера, вес. %0,93 Азот, ч./млн.600Density,, 8756 Distillation interval, ° С: Starting point: boiling point 210 1.0% 338 30% 360 50% 377 70% 398 90% 448 Endpoint, 549 Sulfur, wt. % 0.93 Nitrogen, hours per million 600

сырье подвертают гидроочистке с иопользование.м катализатора, состо щего из глниоземно-кремиеземного носител , содержащего 37 .вес. % кремнезема, 1,8 овес. % ликел , 16 вес. % молибдена. iB зоне реакции поддержевают давление 140 кг1см и температуру в слое катализатора 455° С. Скорость подач.и сырь  4500 баррель, концентраци  водорода гоколо 186 м /баррель, объемна  часова  скорость жидкости 0,70. Потребление водорода ,в системе гидроочистки 1,32% от общего веса сььрь . Данные о выходе и распределении продуктов при гидроочистке приведены в табл. 1. the raw material is hydrotreated using a catalyst consisting of a glyozem-cremiesel carrier containing 37 weight. % silica, 1.8 oats. % liquor, 16 wt. % molybdenum. The iB reaction zone maintains a pressure of 140 kg1 cm and a temperature in the catalyst bed of 455 ° C. The feed rate and raw material are 4500 bbl, the concentration of hydrogen is about 186 m / bbl, the volumetric rate of the liquid is 0.70. The hydrogen consumption in the hydrotreating system is 1.32% of the total weight of the fuel. Data on the yield and distribution of products during hydrotreatment are given in table. one.

т а б л II ц а 1t a b l ii c a 1

ВыходOutput

КомпонентComponent

, л. I барое.1}/ день, l I bar.1} / day

Из табл. 1 следует, что, хот  основнымиFrom tab. 1 it follows that although the main

реакци ми  вл ютс  десульфурирование и денитраци , значительна  часть (Продуктов крекируетс  в низкокип щие углеводороды. В сжиженный (Нефт ной -газ следует ввести 111 баррель/день колцентрата пропана-бутана;The reactions are desulfurization and denitration, a significant part (Products are cracked into low-boiling hydrocarbons. In a liquefied (Oil-gas, 111 barrels / day of propane-butane concentrate should be introduced;

фракцию С7-200° С в колличестве 634 баррель/день следует на1пра1вить на вторую стадию гидрокрекин1га.The C7-200 ° C fraction in the amount of 634 bbl / day should be put on the second stage of hydrocracking.

4,03.5 баррель/день углеводородов, кип щих выше 200° С, служит сырьем дл  д.вухстадийного 1процесса, подаваемым по линии 1. Отношение потока углеводородов, кип щих выше 200° С, к рециркулируемой жидкой фазе первой стадии процесса составл ет 1,6. Указанное выше сырье в линии 1 смешивают с4.03.5 bbl / day of hydrocarbons boiling above 200 ° C is used as feedstock for the two-stage 1 process fed through line 1. The ratio of hydrocarbons boiling above 200 ° C to the recycled liquid phase of the first stage of the process is 1, 6 The above raw materials in line 1 are mixed with

2,400 баррель/день рециркулИруемой жидкой фазой первой стадии, подаваемой по л.инии 2, и с i283 м /баррель рециркулируемого водорода , поступающего ino линии 3.2,400 bbl / day of recirculated liquid phase of the first stage supplied by line 2 and i283 m / bbl of recycled hydrogen coming ino line 3.

Полученна  смесь .направл етс  по линии 1The resulting mixture is directed along line 1

в реактор 4 гидрокрекинга, где поддерживают давление около 141 кг/см .и температуру в слое катализатора около 400° С. Часова  Объем.на  скорость жидкости из расчета 4,035 баррель/день свежего сырь  составл етto the hydrocracking reactor 4, where the pressure is maintained at about 141 kg / cm and the temperature in the catalyst bed is about 400 ° C. The clock volume per fluid rate is 4,035 bbl / day of fresh raw material

0,81. Эфлюент падают по линии 5 в гор чий Сгпаратор 6 при .давлении 146 кг/см и температуре 204° С. В та|бл. 2 приведены .данные D выходе и составе Продуктов, поступающих из реактора 4.0.81. The effluent falls along line 5 to the hot Cgparator 6 at a pressure of 146 kg / cm and a temperature of 204 ° C. In ta | bl. 2 shows the D output data and the composition of the Products coming from the reactor 4.

Таблица 2table 2

ВыходOutput

Основна  «арообразна  фаза, поступающа  .из гор чего сепаратора 6 по линии 7, соедин етс  с напрореатировавщей нафтой вThe main ar-like phase, coming from the hot separator 6 through line 7, is connected to naphtha with naphtha in

SU1812197A 1971-07-12 1972-07-12 The method of producing liquefied petroleum gas SU506302A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US16158671A 1971-07-12 1971-07-12

Publications (1)

Publication Number Publication Date
SU506302A3 true SU506302A3 (en) 1976-03-05

Family

ID=22581812

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (16)

Country Link
US (1) US3718575A (en)
JP (1) JPS5127242B1 (en)
AR (1) AR220881A1 (en)
AU (1) AU458034B2 (en)
BR (1) BR7204613D0 (en)
CA (1) CA978126A (en)
ES (1) ES404746A1 (en)
FR (1) FR2145546B1 (en)
GB (1) GB1391649A (en)
IL (1) IL39832A (en)
IT (1) IT965901B (en)
NL (1) NL7209605A (en)
PL (1) PL89010B1 (en)
SE (1) SE373833B (en)
SU (1) SU506302A3 (en)
ZA (1) ZA724588B (en)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3882014A (en) * 1972-10-26 1975-05-06 Universal Oil Prod Co Reaction zone effluents separation and hydrogen enrichment process
US3847796A (en) * 1973-03-15 1974-11-12 Universal Oil Prod Co Hydrocracking process for the production of lpg
US3917562A (en) * 1974-07-16 1975-11-04 Universal Oil Prod Co Combination process for the conversion of heavy distillates to LPG
US3963600A (en) * 1974-07-16 1976-06-15 Universal Oil Products Company Combination process for the conversion of heavy distillates to LPG
US4247386A (en) * 1979-08-06 1981-01-27 Mobil Oil Corporation Conversion of hydrocarbons to olefins
JPS6238179U (en) * 1985-08-26 1987-03-06
GB2195654A (en) * 1986-09-30 1988-04-13 Shell Int Research Process for recovery of hydrocarbons from a fluid feed
US4875991A (en) * 1989-03-27 1989-10-24 Amoco Corporation Two-catalyst hydrocracking process
US6379533B1 (en) * 2000-12-18 2002-04-30 Uop Llc Hydrocracking process for production of LPG and distillate hydrocarbons
MY135793A (en) 2002-07-12 2008-06-30 Basf Ag Method for the production of butadiene from n-butane
US6953870B2 (en) * 2002-08-26 2005-10-11 Tsoung Y Yan Self-propelled liquid fuel
US8926826B2 (en) * 2011-04-28 2015-01-06 E I Du Pont De Nemours And Company Liquid-full hydroprocessing to improve sulfur removal using one or more liquid recycle streams
SG11201606020PA (en) * 2014-02-25 2016-08-30 Saudi Basic Ind Corp Process for converting hydrocarbons into olefins
CN106062147B (en) * 2014-02-25 2018-07-24 沙特基础工业公司 Method for converting hydrocarbons to alkene
KR20170098867A (en) 2014-12-22 2017-08-30 사빅 글로벌 테크놀러지스 비.브이. Process for producing c2 and c3 hydrocarbons
US10087378B2 (en) 2014-12-22 2018-10-02 Sabic Global Technologies B.V. Process for producing LPG and BTX
SG11201704528TA (en) 2014-12-22 2017-07-28 Sabic Global Technologies Bv Process for producing lpg and btx
CN114350408A (en) 2014-12-22 2022-04-15 沙特基础工业全球技术有限公司 Process for producing C2 and C3 hydrocarbons
EP3390582B1 (en) * 2015-12-15 2024-02-21 SABIC Global Technologies B.V. Process for producing c2 and c3 hydrocarbons

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3047490A (en) * 1958-11-04 1962-07-31 Phillips Petroleum Co Hydrocracking process
US3215617A (en) * 1962-06-13 1965-11-02 Cities Service Res & Dev Co Hydrogenation cracking process in two stages
GB1088933A (en) * 1964-03-10 1967-10-25 British Petroleum Co Improvements relating to the catalytic conversion of hydrocarbons
US3256178A (en) * 1965-05-25 1966-06-14 Union Oil Co Hydrocracking process
US3617483A (en) * 1968-04-25 1971-11-02 Texaco Inc Hydrocracking process
US3607723A (en) * 1969-03-28 1971-09-21 Texaco Inc Split flow hydrocracking process

Also Published As

Publication number Publication date
FR2145546B1 (en) 1978-01-06
AR220881A1 (en) 1980-12-15
IL39832A (en) 1975-04-25
FR2145546A1 (en) 1973-02-23
PL89010B1 (en) 1976-10-30
JPS5127242B1 (en) 1976-08-11
IT965901B (en) 1974-02-11
NL7209605A (en) 1973-01-16
AU4442572A (en) 1974-01-17
ES404746A1 (en) 1975-07-01
IL39832A0 (en) 1972-09-28
GB1391649A (en) 1975-04-23
DE2233826B2 (en) 1975-11-13
AU458034B2 (en) 1975-02-13
SE373833B (en) 1975-02-17
DE2233826A1 (en) 1973-02-08
BR7204613D0 (en) 1973-05-24
ZA724588B (en) 1973-04-25
US3718575A (en) 1973-02-27
CA978126A (en) 1975-11-18

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