Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K3/00—Materials not provided for elsewhere
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
  • B01D53/14—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
  • B01D53/1456—Removing acid components
  • B01D53/1468—Removing hydrogen sulfide
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
  • B01D53/14—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
  • B01D53/1493—Selection of liquid materials for use as absorbents
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
  • B01D2252/10—Inorganic absorbents
  • B01D2252/103—Water
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
  • B01D2252/20—Organic absorbents
  • B01D2252/202—Alcohols or their derivatives
  • B01D2252/2023—Glycols, diols or their derivatives
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
  • B01D2252/20—Organic absorbents
  • B01D2252/202—Alcohols or their derivatives
  • B01D2252/2023—Glycols, diols or their derivatives
  • B01D2252/2025—Ethers or esters of alkylene glycols, e.g. ethylene or propylene carbonate
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
  • B01D2252/20—Organic absorbents
  • B01D2252/204—Amines
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
  • B01D2252/50—Combinations of absorbents
  • B01D2252/504—Mixtures of two or more absorbents
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D2252/00—Absorbents, i.e. solvents and liquid materials for gas absorption
  • B01D2252/60—Additives
• • 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
  • Y02C—CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
  • Y02C20/00—Capture or disposal of greenhouse gases
  • Y02C20/40—Capture or disposal of greenhouse gases of CO2
• • 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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T137/00—Fluid handling
  • Y10T137/0318—Processes
  • Y10T137/0391—Affecting flow by the addition of material or energy

Definitions

• the present invention relates to the absorption of acidic gases from a mixed gas streams containing acidic and non-acidic components.
• the liquid amine stream contained the sorbed acid gas is typically regenerated by desorption of the sorbed gases in a separate tower with the regenerated amine and the desorbed gases leaving the tower as separate streams.
• the various gas purification processes which are available are described, for example, in Gas Purification, Fifth Ed., Kohl and Neilsen, Gulf Publishing Company, 1997, ISBN-13: 978-0-88415-220-0.
• Selective H 2 S removal is applicable to a number of gas treating operations including treatment of hydrocarbon gases from oil sands, coal and shale pyrolysis, refinery gas and natural gas having a low H 2 S/C0 2 ratio and is particularly desirable in the treatment of gases wherein the partial pressure of H 2 S is relatively low compared to that of C0 2 because the capacity of an amine to absorb H 2 S from the latter type gases is very low.
• gases with relatively low partial pressures of H 2 S include synthetic gases made by coal gasification, sulfur plant tail gas and low-Joule fuel gases encountered in refineries where heavy residual oil is being thermally converted to lower molecular weight liquids and gases.
• diisopropylamine is relatively unique among secondary amino alcohols in that its use has been reported, alone or with a physical solvent such as sulfolane, for selective removal of H 2 S from gases containing H 2 S and C0 2 .
• U.K. Patent Publication No. 2,017,524-A (Shell) disclosed that aqueous solutions of dialkylmonoalkanolamines, and particularly ⁇ , ⁇ -diethyl-monoethanolamine (DEAE), have higher selectivity and capacity for H 2 S removal at higher loading levels than MDEA solutions. Nevertheless, even DEAE is not very effective for the low H 2 S loading frequently encountered in the industry. Also, DEAE has a boiling point of 161 ° C, and as such, it is characterized as being a low-boiling, relatively highly volatile amino alcohol. Such high volatilities under most gas scrubbing conditions result in large material losses with consequent losses in economic advantages.
• DEAE dialkylmonoalkanolamines
• DEAE ⁇ , ⁇ -diethyl-monoethanolamine
• a number of severely sterically hindered amino ether compounds notably amino ether alcohols, diamino ethers and alkoxy amino ether alcohols have been developed for the selective removal of H 2 S in the presence of C0 2 .
• U.S. Patents Nos. 4,405,581 ; 4,405,583; 4,405,585, 4,471 , 138 and 4,894, 178 and U.S. Patent Publication 2010/0037775 disclose these highly effective hindered amino ethers, their synthesis and use in selective gas separation processes.
• Specific amino ethers described in these patents include BTEE (bis (ferf.-butylamino-ethoxy)-ethane synthesized from tertiary- butylamine and bis-(2-chloroethoxy)-ethane as well as EEETB (ethoxyethoxyethanol- ferf-butylamine, synthesized from ferf-butylamine and chloroethoxy-ethoxyethanol).
• BTEE bis (ferf.-butylamino-ethoxy)-ethane synthesized from tertiary- butylamine and bis-(2-chloroethoxy)-ethane
• EEETB ethoxyethoxyethanol- ferf-butylamine, synthesized from ferf-butylamine and chloroethoxy-ethoxyethanol.
• U.S. 4,894,178 indicates that a mixture of BTEE and EEETB is particularly effective for the selective separation of H 2 S from C0 2
• 2010/0037775 describes the preparation of alkoxy-substituted etheramines as selective sorbents for separating H 2 S from C0 2. Compared to aqueous MDEA, these severely sterically hindered amines lead to much higher selectivity at high H 2 S loadings
• a liquid, severely sterically hindered, aminoether acid gas absorbent which is subject to freezing in a cold climatic zone by reason of a pour point (ASTM D-97 or equivalent, e.g. Autopour), of -20°C or higher, is rendered freeze-resistant by mixing the aminoether with water prior; the aminoether/water mixture typically contains 10 to 80 more typically 10 to 50, weight percent water, based on the weight of the aminoether although the exact proportions can be adjusted according to the absorbent itself and the projected temperatures during transport, storage and use.
• the amount of water necessary may be as low as 10 or 20 percent for a useful lowering of the pour point..
• the aminoether/water mixture can transported through or into cold climatic zones with reduced risk of freezing and can be stored there without being maintained at a temperature above the freezing point of the aminoether.
• the treated aminoether absorbents in the form of the aqueous mixture can therefore be transported from a first location to a second location in a cold climatic zone for use in an acid gas treatment process with increased convenience. .
• the aminoether/water mixture will be transported from a first, relatively warmer climatic zone which has an ambient temperature at which the aminoether remains unfrozen to a second climatic zone, colder relative to the first zone, which has an ambient temperature below the freezing point of the aminoether itself; the concentration of water in the aminoether/water mixture is adjusted to be sufficient to depress the freezing point of the mixture to a temperature below the ambient temperature of the second climatic zone.
• the aminoether/water mixture can stored at a location in the second climatic zone at a temperature below the freezing point of the aminoether itself, e.g. in an unheated warehouse.
• the proposed transport scheme is applicable to the broad class of liquid amines which may be used for the absorption of acidic gases such as H 2 S and C02 from gas streams such a natural gas, syn gas etc
• the preferred amine sorbents are those which may be used for the selective sorption of H 2 S from acidic gas streams which are mixtures of H 2 S with C0 2 and other acidic gases such as CS 2 , HCN, COS and sulfur derivatives of C-i to C 4 hydrocarbons.
• This preferred class of aminoethers is represented by the derivatives of diethylene glycol or polyethylene glycols which contain severely sterically hindered amino groups as well as by their corresponding derivatives derivatized on the alcohol group to form the corresponding ether or ester derivatives and their corresponding sulfonate and phosphonate salts.
• the preferred severely sterically hindered aminoether derivatives will have a cumulative Es (Taft steric hindrance constant) value greater than 1.75 (see below for further explanation of this constant and its calculation).
• R 1 and R 8 are each C-i to C 8 alkyl and C 2 to C 8 hydroxyalkyl groups
• R 2 , R 3 , R 4 , R 5 , R 6 , and R 7 are each hydrogen, C C 4 alkyl and hydroxyalkyl groups, with certain provisos to define the adequately hindered molecule and m, n, and p are integers from 2 to 4 and o is zero or an integer from 1 to 10.
• a typical diamino ether of this type is 1 ,2- bis(tert-butylaminoethoxy) ethane, a diamino derivative of triethylene glycol.
• US 4,405,585 The hindered amino ether alcohols disclosed in this patent are defined by the formula:
• R 1 is C-
• R 2 , R 3 , R 4 and R 5 are each hydrogen, C-
• x and y are each positive integers from 2 to 4 and z is an integer from 1 to 4.
• This mixture can be prepared in the novel one- step synthesis, by the catalytic tertiary butylamination of a polyalkenyl ether glycol, HO- (CH2CH20) x -CH2CH2-OH, or halo alkoxyalkanol.
• a mixture of bis-(ferf- butylaminoethoxy)ethane (BTEE) and ethoxyethoxyethanol-ferf-butylamine (EEETB) can be obtained by the catalytic ferf-butylamination of triethylene glycol.
• This mixture can be prepared in the one-step synthesis, by the catalytic ferf-butylamination of the corresponding polyalkenyl ether glycol, for example, by the catalytic ferf-butylamination of triethylene glycol.
• This mixture is one of the preferred absorbents for use in offshore gas processing.
• US 2010/0037775 The reaction of a polyalkenyl ether glycol with a hindered amine such as ferf-butylamine to form useful aminother absorbents is improved by the use of an alkoxy-capped glycol in order to preclude the formation of an unwanted cyclic by-product, ferf-butyl morpholine (TBM).
• a preferred capped glycol is methoxy- triethylene glycol although the ethoxy-, propoxy- and butoxy homologs may also be used.
• the reaction between triethylene glycol and ferf-butylamine is shown to produce a mixture of bis-(ferf-butylaminoethoxy) ethane and ferf-butylaminoethoxyethoxyethanol in a weight ratio of about 65-67%: 33% for a total yield of about 95% of the mixture over an extended reaction time while the reaction with the alkoxy-capped glycol produces the mono-amino reaction product in comparable yield after a significantly shorter reaction time.
• the aminoether compounds may be used in conjunction with other related materials such as an amine salt as described in U.S. Patent No. 4,618,481.
• the severely sterically hindered amino compound can be a secondary amino ether alcohol or a disecondary amino ether.
• the amine salt can be the reaction product of the severely sterically hindered amino compound, a tertiary amino compound such as a tertiary alkanolamine or a triethanolamine, with a strong acid, or a thermally decomposable salt of a strong acid, i.e., ammonium salt or a component capable of forming a strong acid.
• U.S. Pat. No. 4,892,674 discloses a process for the selective removal of H 2 S from gaseous streams using an absorbent composition comprising a non- hindered amine and an additive of a severely-hindered amine salt and/or a severely- hindered aminoacid.
• the amine salt is the reaction product of an alkaline severely hindered amino compound and a strong acid or a thermally decomposable salt of a strong acid, i.e., ammonium salt.
• a preferred class of aminoethers for offshore application is defined by the formula:
• R 1 is a secondary or tertiary alkyl group of 3 to 8 carbon atoms, preferably a tertiary group of 4 to 8 carbon atoms
• Y is H or alkyl of 1 to 6 carbon atoms
• n is a positive integer from 3 to 8
• x is a positive integer from 3 to 6.
• the preferred R 1 group is tertiary butyl and the most preferred amino ethers are those derived from triethylene glycol (n is 2, x is 3).
• the amino ether is an amino ether alcohol such as tert-butylamino ethoxyethoxyethanol, derived from triethylene glycol; when Y is alkyl, preferably methyl, the amino ether is an alkoxy amino ether, with preference for tert-butylamino methoxy-ethoxyethoxyethanol.
• the monoamino ethers may be used in blends with diamino ethers in which the terminal OH group of the ether alcohol or the terminal alkoxy group of the alkoxy amino ether is replaced by a further hindered amino group as expressed in the formula:
• R 1 , n and x are as defined above and R 2 , which may the same or different to R 1 , is a secondary or tertiary alkyl group of 3 to 8 carbon atoms.
• a preferred diamino ether of this type is bis-(t-butylamino ethoxy) ethane which may conveniently be used as a mixture with tert-butylamino methoxy-ethoxyethoxyethanol in a weight ratio of about 65- 67wt%: 33-35wt%.
• the severely sterically hindered secondary aminoether mentioned above are characterized by acyclic or cyclic moieties attached to the amino nitrogen atom(s).
• the term "severely sterically hindered” signifies that the nitrogen atom of the amino moiety is attached to one or more bulky carbon groupings.
• the severely sterically hindered aminoether alcohols have a degree of steric hindrance such that the cumulative E s value (Taft's steric hindrance constant) greater than 1 .75 as calculated from the values given for primary amines in Table V in D. F. DeTar, Journal of Organic Chemistry, 45, 5174 (1980), to which reference is made for a description of this parameter.
• Another means for determining whether a secondary amino compound is "severely sterically hindered” is by measuring its 15N nuclear magnetic resonance (NMR) chemical shift. It has been found that the sterically hindered secondary amino compounds have a 15N NMR chemical shift greater than about ⁇ +40 ppm, when a 90% by wt. amine solution in 10% by wt. D 2 0 at 35°C is measured by a spectrometer using liquid (neat) ammonia at 25°C. as a zero reference value. Under these conditions, the tertiary amino compound used for comparison, methyldiethanolamine, has a measured 15N NMR chemical shift value of 527.4.
• NMR nuclear magnetic resonance
• 2-(2-tertiarybutylamino) propoxyethanol, 3-(tertiarybutylamino)-1-propanol, 2-(2-isopropylamino)-propoxyethanol and tertiarybutylaminoethoxyethanol had measured 15N NMR chemical shift values of ⁇ +74.3, ⁇ +65.9, ⁇ +65.7 and ⁇ +60. 5 ppm, respectively, whereas the ordinary sterically hindered amine, secondary-butylaminoethoxyethanol and the non-sterically hindered amine, n-butylaminoethoxyethanol had measured 15N NMR chemical shift values of . ⁇ +48.9 and 635.8 ppm, respectively.
• the sterically hindered aminoether absorbents which require special attention during cold storage, transport and use are those which have a Pour Point (ASTM D-97 or equivalent) of -20°C or higher. Absorbents with lower pour points generally present no problem and accordingly it is not normally considered necessary for them to be mixed with water before shipping out from the manufacturing location. Mixtures of aminoether absorbents may require treatment with water if their freeze points vary below those of the individual components of the mixtures having adequately low freeze/pour points.
• the aminoether absorbent or mixture of aminoether absorbents is blended with water to confer the desired resistance to freezing during shipping and storage. While the use of other suitable pour point depressants would be similarly effective, the use of water is particularly attractive since the amines are typically used in the form of an aqueous solution; shipping with the added water therefore avoids the use of other possibly expensive additives.
• Exemplary freezing points for H 2 S selective hindered aminoether absorbents are:
• MEEETB Methoxy ethoxyethoxyethanol -f-butylamine
• Bis(f-butylamino) triethylene glycol (BisTEGTB) 91.6 wt% purity, with triethylene glycol (TEG) 0.5 wt%; triethylene glycol-f- butylamine (TEGTB) 5.75 wt%.
• Bis-TEGTB 34.9 wt%.
• Bis-TEGTB 34.9 wt%.
• the water in an amount from about 10-50, preferably 20-40, weight percent, based on the weight of the amine, is simply blended into the liquid aminoether using conventional mixing techniques, e.g., stirred tank mixer.
• the blended water/aminoether is then readied for shipping, for example, by loading into 200-I drums, ISO liquid containers, bulk liquid containers, Flexitanks, road tank trucks, rail tank cars, etc.
• the blended liquid is then shipped to the cold climatic location using conventional means without the need for maintaining it at temperatures above freezing.
• the aminoether/water blend can be diluted if necessary to the final desired concentration, typically from 5 to 30 v/v percent, and used in the absorption process. Alternatively, it can be stored in an unheated location until wanted for use.
• the present transport scheme is useful when the aminoether is to be shipped through a climatic zone where sub-freezing temperatures for the aminoether, typically below about 0°C, prevail. It is especially useful when shipping through a zone where the temperature is expected to be more than -10 °C below the freezing temperature of the aminoether, especially when temperatures more than -20 °C below the freezing point of the aminoether are expected..
• the amount of water required to confer resistance to freezing will depend upon the identity of the aminoether. As noted above, 10 to 45 wt. percent is normally sufficient with amounts within this range varying according to the undiluted freezing point of the aminoether

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  • 2013-03-11 US US13/793,298 patent/US9458367B2/en not_active Expired - Fee Related
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