US3481866A - Extraction of lead from petroleum products employing aqueous iodine monochloride - Google Patents

Extraction of lead from petroleum products employing aqueous iodine monochloride Download PDF

Info

Publication number
US3481866A
US3481866A US675774A US3481866DA US3481866A US 3481866 A US3481866 A US 3481866A US 675774 A US675774 A US 675774A US 3481866D A US3481866D A US 3481866DA US 3481866 A US3481866 A US 3481866A
Authority
US
United States
Prior art keywords
lead
extraction
iodine monochloride
petroleum products
gasoline
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
US675774A
Inventor
Ronald Moss
Kenneth Campbell
Samuel T Griffiths
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.)
Innospec Ltd
Original Assignee
Associated Octel Co Ltd
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
Priority claimed from GB3798467A external-priority patent/GB1126630A/en
Application filed by Associated Octel Co Ltd filed Critical Associated Octel Co Ltd
Application granted granted Critical
Publication of US3481866A publication Critical patent/US3481866A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • C10G21/00Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents
    • C10G21/06Refining of hydrocarbon oils, in the absence of hydrogen, by extraction with selective solvents characterised by the solvent used
    • C10G21/08Inorganic compounds only

Definitions

  • This invention relates to the extraction of lead from hydrocarbon feedstock, gasoline and other petroleum products.
  • lead compounds especially lead alkyls such as tetraethyl lead and tetramethyl lead
  • gasoline and other petroleum products is common practice.
  • the gasoline is to be subjected to reprocessing, for example, in a catalytic reformer in which the gasoline may be used as a feedstock or feedstock supplement.
  • the lead be reduced to as low a level as possible, preferably to below 50 parts per thousand million, in order to minimise poisoning of the catalyst, which is usually platinum.
  • a method of extracting lead from gasoline and other petroleum products which, being quick and substantially 100% eflicient, is capable of application on a large scale.
  • the invention is based on the discovery that lead alkyls in gasoline or other petroleum products will react quantitatively with iodine monochloride to form water soluble dialkyl lead halides.
  • the method of the present invention therefore comprises treating the lead alkyl containing gasoline or other lead alkyl containing petroleum product with an aqueous solution of iodine monochloride, thoroughly mixing the inorganic phase with the organic phase, and separating the organic phase from the inorganic phase.
  • the amount of iodine monochloride can be stoichiometric in relation to the amount of lead alkyl present in the petroleum product. More usually, however, the amount of iodine monochloride used will be in excess of stoichiometric.
  • the concentration of the iodine monochloride solution used in the method of the invention will, of course, vary 3,481,866 Patented Dec. 2, 1969 with the volume of gasoline or petroleum product to be treated. As a matter of convenience the solutions used will usually be in the range 0.1-2.0 molar. Where the petroleum product contains any significant amount of olefin higher amounts of iodine monochloride will be used because iodine monochloride reacts readily with an olefinic double bond.
  • the extraction is performed quite conveniently at room temperature.
  • test samples were made up by blending various proportions of virgin naphtha, isooctane and kerosine.
  • the samples were made up to simulate petroleum ranging from a typical catalytic reformer feedstock on the one hand to an aviation turbine fuel on the other.
  • a known quantity of lead alkyl either tetramethyl lead, tetraethyl lead or a mixed lead alkyl obtained by a rearrangement reaction of tetraethyl lead and tetramethyl lead, was added to each sample.
  • the invention is particularly applicable to the extraction of lead from catalytic reformer feedstocks, it may also be applied to the extraction of lead from a Wide range of petroleum products ranging from crude oil to light petroleum fractions.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Inorganic Chemistry (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

United States Patent l U.S. Cl. 208-251 4 Claims ABSTRACT OF THE DISCLOSURE Lead alkyl containing petroleum products, particularly gasoline and catalytic reformer feedstocks, are freed from their lead content by treatment with aqueous iodine monochloride.
This invention relates to the extraction of lead from hydrocarbon feedstock, gasoline and other petroleum products.
The addition of lead compounds, especially lead alkyls such as tetraethyl lead and tetramethyl lead, to gasoline and other petroleum products is common practice. For certain purposes it is necessary subsequently to extract the lead from the gasoline. For example it may be necessary to extract the lead if the gasoline is to be subjected to reprocessing, for example, in a catalytic reformer in which the gasoline may be used as a feedstock or feedstock supplement. In this case it is important that the lead be reduced to as low a level as possible, preferably to below 50 parts per thousand million, in order to minimise poisoning of the catalyst, which is usually platinum.
Known methods for the extraction of lead from petroleum products involve the extraction of the lead by treatment of the leaded product with hydrochloric or sulphuric acid. The former procedure forms the basis of the standard methods for the determination of lead in gasoline, IP 96/64 and ASTM D526. Whilst these methods are satisfactory for analytical purposes and small scale operations they are not suitable for application on a large scale.
In accordance with the present invention a method of extracting lead from gasoline and other petroleum products has been found which, being quick and substantially 100% eflicient, is capable of application on a large scale. The invention is based on the discovery that lead alkyls in gasoline or other petroleum products will react quantitatively with iodine monochloride to form water soluble dialkyl lead halides.
The method of the present invention therefore comprises treating the lead alkyl containing gasoline or other lead alkyl containing petroleum product with an aqueous solution of iodine monochloride, thoroughly mixing the inorganic phase with the organic phase, and separating the organic phase from the inorganic phase. By this method substantially complete extraction of the lead from the organic phase into the inorganic phase is obtained leaving the gasoline or other petroleum product substantially free of lead.
Since the reaction of the iodine monochloride with the lead alkyl is quantitative the amount of iodine monochloride can be stoichiometric in relation to the amount of lead alkyl present in the petroleum product. More usually, however, the amount of iodine monochloride used will be in excess of stoichiometric.
The concentration of the iodine monochloride solution used in the method of the invention will, of course, vary 3,481,866 Patented Dec. 2, 1969 with the volume of gasoline or petroleum product to be treated. As a matter of convenience the solutions used will usually be in the range 0.1-2.0 molar. Where the petroleum product contains any significant amount of olefin higher amounts of iodine monochloride will be used because iodine monochloride reacts readily with an olefinic double bond.
The extraction is performed quite conveniently at room temperature.
In order to demonstrate the extraction of lead alkyls from petroleum products in accordance with this invention a number of test samples were made up by blending various proportions of virgin naphtha, isooctane and kerosine. The samples were made up to simulate petroleum ranging from a typical catalytic reformer feedstock on the one hand to an aviation turbine fuel on the other. A known quantity of lead alkyl, either tetramethyl lead, tetraethyl lead or a mixed lead alkyl obtained by a rearrangement reaction of tetraethyl lead and tetramethyl lead, was added to each sample.
Various volumes of each sample Were taken and shaken at room temperature in a separating funnel with 10 ml. portions of a 1.0 molar aqueous solution of iodine monochloride. After shaking for three minutes the inorganic phase was separated and the organic phase washed three times with 10 ml. portions of water. The washings were added to the separated inorganic phase and the lead content of the collected inorganic phase was determined colorimetrically by the well known dithizonate procedure. The results were as follows, the weight of lead extracted is the average of two determinations.
These results clearly demonstrate the substantially complete extraction which is achieved by the method of the present invention. They also clearly demonstrate the efliciency of a single extraction which is maintained even with sample: extractant ratios as high as :1.
Whilst the invention is particularly applicable to the extraction of lead from catalytic reformer feedstocks, it may also be applied to the extraction of lead from a Wide range of petroleum products ranging from crude oil to light petroleum fractions.
We claim:
1. The process which comprises treating a petroleum product containing lead alkyl with an aqueous solution of iodine monochloride, thoroughly mixing the inorganic phase with the organic phase, and subsequently separating the two phases, thereby removing the lead from the said petroleum product.
2. The process of claim 1, wherein the amount of iodine monochloride used to treat the lead alkyl-containing petroleum product is in excess of the stoichiometric amount required to react with the lead alkyl in the product under treatment.
3. The process of claim 1 wherein the iodine monochloride solution used is 0.1-2.0 molar.
4. The process of claim 1, wherein the lead alkyl- FOREIGN PATENTS containing product under treatment is a catalytic reformer 1 126 1968 Great Britain feedstock.
References Clted DELBERT E. GANTZ, Primary Examiner UNITED STATES PATENTS 5 J. N. NELSON, Assistant Examiner 2,504,134 5/1948 Kharasch 196-44 2,969,320 1/1961 Shapiro et a1 208251 US. Cl. X.R.
2,729,593 1/1956 Garwood 196-35 20888
US675774A 1967-08-17 1967-10-17 Extraction of lead from petroleum products employing aqueous iodine monochloride Expired - Lifetime US3481866A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB3798467A GB1126630A (en) 1967-08-24 1967-08-17 Extraction of lead from petroleum products
DEA0056594 1967-08-24

Publications (1)

Publication Number Publication Date
US3481866A true US3481866A (en) 1969-12-02

Family

ID=25964467

Family Applications (1)

Application Number Title Priority Date Filing Date
US675774A Expired - Lifetime US3481866A (en) 1967-08-17 1967-10-17 Extraction of lead from petroleum products employing aqueous iodine monochloride

Country Status (2)

Country Link
US (1) US3481866A (en)
DE (1) DE1645688A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4424119A (en) 1976-12-27 1984-01-03 Mobil Oil Corporation Process for removal of alkyl lead impurities from liquid hydrocarbons
US4424120A (en) 1976-12-27 1984-01-03 Mobil Oil Corporation Process for removal of alkyl lead impurities from liquid hydrocarbons

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2504134A (en) * 1948-05-04 1950-04-18 Us Army Deleading of gasoline
US2729593A (en) * 1953-01-06 1956-01-03 Socony Mobil Oil Co Inc Demetalation of hydrocarbon oils
US2969320A (en) * 1959-02-03 1961-01-24 Socony Mobil Oil Co Inc Removal of tetraethyl lead from hydrocarbon liquids with sulfur dioxide
GB1126630A (en) * 1967-08-24 1968-09-11 Ass Octel Extraction of lead from petroleum products

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2504134A (en) * 1948-05-04 1950-04-18 Us Army Deleading of gasoline
US2729593A (en) * 1953-01-06 1956-01-03 Socony Mobil Oil Co Inc Demetalation of hydrocarbon oils
US2969320A (en) * 1959-02-03 1961-01-24 Socony Mobil Oil Co Inc Removal of tetraethyl lead from hydrocarbon liquids with sulfur dioxide
GB1126630A (en) * 1967-08-24 1968-09-11 Ass Octel Extraction of lead from petroleum products

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4424119A (en) 1976-12-27 1984-01-03 Mobil Oil Corporation Process for removal of alkyl lead impurities from liquid hydrocarbons
US4424120A (en) 1976-12-27 1984-01-03 Mobil Oil Corporation Process for removal of alkyl lead impurities from liquid hydrocarbons

Also Published As

Publication number Publication date
DE1645688A1 (en) 1970-07-30

Similar Documents

Publication Publication Date Title
Skinner Chemical state of vanadium in Santa Maria Valley crude oil
Faragher et al. Quantitative determination of sulfur and sulfur derivatives of hydrocarbons in naptha solutions and in petroleum distillates
Cady et al. Composition of shale oil
US3481866A (en) Extraction of lead from petroleum products employing aqueous iodine monochloride
US2068850A (en) Process of improving gasoline
US2257086A (en) Treating hydrocarbon fluids
US2563369A (en) Refining fuel oil
US2970105A (en) Treatment of hydrocarbon oils
US3190829A (en) Process for removing metals from a mineral oil with an alkyl sulfonic acid
US3583906A (en) Aromatic extraction process with diglycolamine solvent
Poirier et al. Method for determining the olefinic content of the saturated and aromatic fraction of petroleum distillates by hydroboration
CA3061083C (en) Prevention of the emission of hydrogen sulphide in the production of hot bitumen or asphalt
US3052626A (en) Treatment of petroleum products
Thompson et al. Identification of Some Chain Sulfides in a Wasson, Texas, Crude Oil Distillate Boiling from 111° to 150° C.
Kartsev Geochemical transformation of petroleum
US2919245A (en) Treatment of organic materials
RU2786756C1 (en) Method for preparing samples of petroleum chemical reagents for determining organochlorogenic compounds and organically bound chlorine and method for determining organochlorogenic compounds in sample of petroleum chemical reagent
US3804749A (en) Process for desulfurization of chemical media or of materials containing sulfur and/or its derivatives
Hamor et al. The Technical Examination of Crude Petroleum, Petroleum Products and Natural Gas: Including Also the Procedures Employed in the Evaluation of Oil-shale and the Laboratory Methods in Use in the Control of the Operation of Benzol-recovery Plants
Linton ON THE TECHNICAL ANALYSIS OF ASPHALTUM.
US2710855A (en) Extractive crystallization processes
RU2790059C1 (en) Method for preparing samples of oilfield chemicals for the determination of organochlorine compounds
Poth et al. The Estimation of Nitrogen in Petroleum and Bitumens1
RU2777703C1 (en) Method for preparing samples of oilfield chemicals for the determination of organochlorine compounds
US1766338A (en) Method of refining liquid hydrocarbons