阅读说明：本技术 改进的杂质去除方法 (Improved impurity removal process ) 是由 斯泰恩·范德维弗 罗宾·马顿 克拉斯·维克托 于 2019-02-13 设计创作，主要内容包括：公开了一种方法,该方法包含：步骤a)使包含杂质的进料流与吸收剂流在对向流中接触,以产生杂质贫化的产物流和杂质富集的吸收剂流,杂质贫化的产物流在杂质的摩尔量上相对于进料流中的该杂质的摩尔量是贫化的,杂质富集的吸收剂流在杂质的摩尔量上相对于吸收剂流中的该杂质的摩尔量是富集的；步骤b)处理杂质富集的吸收剂流,以形成包含该杂质的气体流以及再生的吸收剂流,再生的吸收剂流在杂质的摩尔量上相对于杂质富集的吸收剂流中该杂质的摩尔量是贫乏的；本文所述的吸收剂流包含至少15wt％的至少一种通式(I)的化合物(A)或一种混合物(M),混合物(M)包含至少一种通式(II)的化合物(B)以及至少一种通式(III)的化合物(C)。(A method is disclosed, the method comprising: step a) contacting a feed stream comprising an impurity with an absorbent stream in a counter stream to produce an impurity-depleted product stream that is depleted in molar mass of the impurity relative to the molar mass of the impurity in the feed stream and an impurity-enriched absorbent stream that is enriched in molar mass of the impurity relative to the molar mass of the impurity in the absorbent stream; step b) treating the impurity-enriched absorbent stream to form a gas stream comprising the impurity and a regenerated absorbent stream that is depleted in molar amount of the impurity relative to the molar amount of the impurity in the impurity-enriched absorbent stream; the absorbent stream described herein comprises at least 15 wt% of at least one compound (a) of the general formula (I) or one mixture (M) comprising at least one compound (B) of the general formula (II) and at least one compound (C) of the general formula (III).)

1. A method, comprising:

step a) contacting a feed stream comprising an impurity with an absorbent stream in a counter stream to produce an impurity-depleted product stream that is depleted in molar mass of the impurity relative to the molar mass of the impurity in the feed stream and an impurity-enriched absorbent stream that is enriched in molar mass of the impurity relative to the molar mass of the impurity in the absorbent stream;

step b) treating the impurity-enriched absorbent stream to form a gas stream comprising the impurities and a regenerated absorbent stream that is depleted in molar amounts of the impurities relative to the molar amounts of the impurities in the impurity-enriched absorbent stream;

wherein the absorbent stream comprises:

i. at least 15 weight percent (hereinafter wt%) of at least one substituted 2-pyrrolidone of general formula (I) [ hereinafter compound (a) ] relative to the total weight of the absorbent stream:

wherein:

-R₁and R₂Each of which, equal to or different from each other, and at each occurrence, is independently selected from H or CH₃；

-each R is the same or different from each other and, at each occurrence, is selected from H or CH₃；

-i is an integer ranging from 0 to 3;

-o is an integer ranging from 2 to 6; n is an integer ranging from 0 to 4; m is an integer ranging from 0 to 4;

alternatively, the first and second electrodes may be,

a mixture [ hereinafter mixture (M) ] comprising at least one substituted 2-pyrrolidone of formula (II) herein below [ hereinafter compound (B) ] and at least one amine compound of formula (III) herein below [ hereinafter compound (C) ]:

wherein:

-each R' is the same or different from each other and, at each occurrence, is independently selected from H or CH₃

-j is an integer ranging from 0 to 3

-R₃、R₄、R₅And R₆Each of which, equal to or different from each other, and at each occurrence, is independently selected from H or CH₃；

-q is an integer ranging from 0 to 1; p is an integer ranging from 1 to 6; with the proviso that when p is 1 and q is 0, then R₃And R₄Is CH₃When p + q is 2, then R₃、R₄、R₅Or R₆Is CH₃；

-R₇、R₈And R₉Each of which, equal to or different from each other, and at each occurrence, is independently selected from H, C_1-10Alkyl radical, C_1-10Alkoxy radicalAlcohols or C_1-10An alkanol group; with the proviso that R₇、R₈Or R₉At least one of which is C_1-10Alkoxy alcohols or C_1-10And (3) alkanol groups.

2. The process according to claim 1, wherein the absorbent stream comprises a mixture (M) comprising at least one compound (B) and at least one compound (C), wherein the at least one compound (B) is selected from those of the following formula (II-B) herein:

wherein:

-p is an integer ranging from 2 to 6.

3. The process according to claim 1 or 2, wherein the absorbent stream comprises the mixture (M) comprising at least one compound (B) and at least one compound (C), wherein the compound (B) is selected from those of formulae (II-C) to (II-g) as herein below:

4. the process according to any one of claims 1 to 3, wherein the absorbent stream comprises the mixture (M) comprising at least one compound (B) and at least one compound (C), wherein the compound (C) is selected from: primary, secondary and tertiary alkanolamines, or mixtures of two or more thereof.

5. Process according to any one of claims 1 to 4, wherein the absorbent stream comprises the mixture (M) comprising at least one compound (B) and at least one compound (C), wherein the weight percentage of the compound (B) comprised in the mixture (M) with respect to the total weight of the mixture (M) is: equal to or greater than 5 wt%, preferably equal to or greater than 10 wt%, more preferably equal to or greater than 15 wt%, more preferably equal to or greater than 18 wt%, more preferably equal to or greater than 20 wt%, even more preferably equal to or greater than 22 wt%, and equal to or less than 50 wt%, preferably equal to or less than 45 wt%, more preferably equal to or less than 40 wt%, more preferably equal to or less than 35 wt%, more preferably equal to or less than 30 wt%, even more preferably equal to or less than 28 wt%.

6. Process according to any one of claims 1 to 5, wherein the absorbent stream comprises the mixture (M) comprising at least one compound (B) and at least one compound (C), wherein the weight percentage of the compound (C) comprised in the mixture (M) with respect to the total weight of the mixture (M) is: equal to or greater than 2 wt%, preferably equal to or greater than 5 wt%, preferably equal to or greater than 10 wt%, more preferably equal to or greater than 20 wt%, even more preferably equal to or greater than 30 wt%, yet even more preferably equal to or greater than 40 wt%, most preferably equal to or greater than 45 wt%, and equal to or less than 70 wt%, preferably equal to or less than 65 wt%, more preferably equal to or less than 60 wt%, even more preferably equal to or less than 55 wt%.

7. Process according to any one of claims 1 to 6, wherein said absorbent stream comprises said mixture (M), wherein said mixture (M) further comprises water, said water being added to said mixture (M) in an amount corresponding to the weight ratio of said water to said compound (B) which is: at least 0.25:1, preferably at least 0.3:1, more preferably at least 0.4:1, even more preferably at least 0.6:1, yet even more preferably at least 0.9:1, it being further understood that the weight ratio of said water to said compound (B) in said absorbent stream is generally at most 4:1, preferably at most 3:1, more preferably at most 2.5:1, even more preferably at most 2:1, yet even more preferably at most 1.1: 1.

8. The process according to claim 1, wherein the absorbent stream comprises at least 15 wt% of the at least one compound (a), wherein the at least one compound (a) is selected from those of formula (I-a) herein below:

wherein:

-o is an integer ranging from 2 to 4; n is an integer selected from 0 or 1; m is an integer selected from 0 or 1.

9. The process according to claim 8, wherein said absorbent stream comprises a composition [ hereinafter composition (C) ] comprising at least 15% by weight of said at least one compound (A), of at least one compound (C) and of water, relative to the total weight of said composition (C).

10. The process according to claim 9, wherein the absorbent stream comprises the composition (C), wherein the weight ratio of the water to the compound (a) is: at least 0.25:1, preferably at least 0.3:1, more preferably at least 0.4:1, even more preferably at least 0.6:1, yet even more preferably at least 0.9:1, and at most 4:1, preferably at most 3:1, more preferably at most 2.5:1, even more preferably at most 2:1, yet even more preferably at most 1.1: 1.

11. Process according to claim 9 or 10, wherein the absorbent stream comprises the composition (C), wherein the weight percentage of the compound (a) contained in the composition (C) with respect to the total weight of the composition (C) is: equal to or greater than 18 wt%, preferably equal to or greater than 20 wt%, more preferably equal to or greater than 21 wt%, even more preferably equal to or greater than 22 wt%, and equal to or less than 50 wt%, preferably equal to or less than 40 wt%, more preferably equal to or less than 35 wt%, even more preferably equal to or less than 30 wt%, even more preferably equal to or less than 29 wt%, most preferably equal to or less than 28 wt%.

12. The process according to any one of claims 9 to 11, wherein the absorbent stream comprises the composition (C), wherein the weight percentage of the compound (C) comprised in the composition (C) with respect to the total weight of the composition (C) is: equal to or greater than 2 wt%, preferably equal to or greater than 5 wt%, preferably equal to or greater than 10 wt%, more preferably equal to or greater than 20 wt%, even more preferably equal to or greater than 30 wt%, yet even more preferably equal to or greater than 40 wt%, most preferably equal to or greater than 45 wt%, and equal to or less than 85 wt%, preferably equal to or less than 80 wt%, more preferably equal to or less than 75 wt%, more preferably equal to or less than 70 wt%, more preferably equal to or less than 65 wt%, even more preferably equal to or less than 60 wt%, yet even more preferably equal to or less than 55 wt%.

13. The process of any one of claims 1 to 12, wherein the absorbent stream further comprises a promoter selected from the group consisting of: amines, alcohols, ketones, vinyl alcohols, vinyl ketones, ether alcohols, ether ketones, glycols, polyethylene glycols, polypropylene glycols, ethylene glycol propylene glycol copolymers, glycol ethers, mercapto glycols, thiols, sulfones, sulfoxides, N-alkylated 2-pyrrolidones, N-alkylated piperidones, cyclotetramethylene sulfones, N-alkyl formamides, N-alkyl acetamides, alkyl phosphates, alkylene carbonates and/or dialkyl carbonates, and combinations or mixtures thereof.

14. The process of claim 13, wherein the absorbent stream comprises 0.1-20 wt% promoter.

15. The process of any of claims 1 to 14, wherein the molar amount of the impurity in the impurity-depleted product stream is reduced by at least 5%, preferably at least 10%, more preferably at least 20%, even more preferably at least 30%, yet even more preferably at least 40%, most preferably at least 50% relative to the molar amount of the impurity in the feed stream, and wherein the molar amount of the impurity in the enriched absorbent stream is increased by at least 5%, preferably at least 10%, more preferably at least 20%, even more preferably at least 30%, yet even more preferably at least 40%, most preferably at least 50% relative to the molar amount of the impurity in the absorbent stream.

16. A mixture (M) comprising at least one substituted 2-pyrrolidone of the general formula (II) herein below [ hereinafter compound (B) ] and at least one amine compound of the general formula (III) herein below [ hereinafter compound (C) ]:

wherein:

-each R' is the same or different from each other and, at each occurrence, is independently selected from H or CH₃

-j is an integer ranging from 0 to 3

-R₃、R₄、R₅And R₆Each of which, equal to or different from each other, and at each occurrence, is independently selected from H or CH₃；

-q is an integer ranging from 0 to 1; p is an integer ranging from 1 to 6; with the proviso that when p is 1 and q is 0, then R₃And R₄Is CH₃When p + q is 2, then R₃、R₄、R₅Or R₆Is CH₃；

-R₇、R₈And R₉Each of which, equal to or different from each other, and at each occurrence, is independently selected from H, C_1-10Alkyl radical, C_1-10Alkoxy alcohols or C_1-10An alkanol group; with the proviso that R₇、R₈Or R₉At least one of which is C_1-10Alkoxy alcohols or C_1-10And (3) alkanol groups.

17. An absorbent stream comprising a mixture (M) as defined in claim 16.

18. An impurity enriched absorbent streamComprising at least one absorbed impurity selected from the group consisting of: hydrogen sulfide (H)₂S), carbon dioxide (CO)₂) Carbon Oxysulfide (COS), carbon disulfide (CS)₂) Disulfide or mercaptan, the absorbent stream comprising:

i. at least 15 wt%, relative to the total weight of the absorbent stream, of at least one substituted 2-pyrrolidone of general formula (I) [ hereinafter compound (a) ]:

wherein:

-R₁and R₂Each of which, equal to or different from each other, and at each occurrence, is independently selected from H or CH₃；

-each R is the same or different from each other and, at each occurrence, is selected from H or CH₃；

-i is an integer ranging from 0 to 3;

-o is an integer ranging from 2 to 6; n is an integer ranging from 0 to 4; m is an integer ranging from 0 to 4;

alternatively, the first and second electrodes may be,

a mixture [ hereinafter mixture (M) ] comprising at least one substituted 2-pyrrolidone of formula (II) herein below [ hereinafter compound (B) ] and at least one amine compound of formula (III) herein below [ hereinafter compound (C) ]:

wherein:

-each R' is the same or different from each other and, at each occurrence, is independently selected from H or CH₃

-j is an integer ranging from 0 to 3

-R₃、R₄、R₅And R₆Each of which, equal to or different from each other, and at each occurrence, is independently selected from H or CH₃；

-q is an integer ranging from 0 to 1; p is an integer ranging from 1 to 6; with the proviso that when p is 1 and q is 0, then R₃And R₄Is CH₃When p + q is 2, then R₃、R₄、R₅Or R₆Is CH₃；

-R₇、R₈And R₉Each of which, equal to or different from each other, and at each occurrence, is independently selected from H, C_1-10Alkyl radical, C_1-10Alkoxy alcohols or C_1-10An alkanol group; with the proviso that R₇、R₈Or R₉At least one of which is C_1-10Alkoxy alcohols or C_1-10And (3) alkanol groups.

Technical Field

The present invention relates to an improved process for the removal of impurities, particularly other impurities (e.g. H)₂S and CO₂) In the presence of a catalyst, mercaptan removal is improved from a non-aqueous process stream that is primarily a gas, but also includes a liquid.

Background

It is known that it is important to remove impurities, such as hydrogen sulfide (H), from various feed streams, particularly gaseous feed streams₂S), carbon dioxide (CO)₂) Carbon Oxysulfide (COS), carbon disulfide (CS)₂) Disulfides and thiols.

Such feed streams occur in the processing of, for example, natural gas. The gas from a natural gas field contains mainly methane and may also contain significant amounts of impurities such as carbon dioxide (easily up to 70 vol.%), hydrogen sulphide, mercaptans and carbonyl sulphide. Therefore, it may be desirable to remove these impurities to reduce further transportation costs as compressed gas, to mitigate corrosion risks in downstream systems and pipelines, to adjust the heating value of the gas to suit consumer needs, and/or to enable liquefaction of natural gas into liquefied natural gas lng (liquefied natural gas), an increasingly widely used means of transportation to transport natural gas from remote acquisition sites to the natural gas consumption market.

Removal of impurities is also important in refinery streams, such as LPG fractions, off-gases from Fluid Catalytic Cracking (FCC), hydrotreater off-gases, and refinery gases typically contain significant amounts of mercaptans and/or H₂S is in oneIn some cases CO may also be present₂. The distillate fractions for different fuel cells need to be desulfurized to alleviate the acid rain problem caused by SOx emissions in the flue gas after combustion. Thus, several of these liquid fractions are subjected to hydrodesulfurization, which is the conversion of heavy sulfur compounds into gaseous H₂And S refining. H collected from all these sources in a so-called Claus plant₂S can subsequently be converted to elemental sulphur, which has become a commercial product, for example as a feedstock for the production of sulphuric acid.

In addition, in the main consisting of H₂CO and possibly N₂Impurity removal can be important in the production of compositional syngas, which is a variety of forms of gas that are important chemical building blocks, but also important intermediates in the energy conversion from solid carbonaceous streams (e.g., solid waste streams, tar sands, oil shale, etc.). It is often desirable to remove mercaptans, H, from syngas₂S and CO₂Since mercaptans and H₂S may be an undesirable reactant therein, and/or cause the evolution of sulfur oxides (SOx) upon combustion, which is undesirable in view of acid rain concerns, and because of CO₂It is possible, for example, to charge the downstream process with interfering inerts.

However, simultaneous and efficient removal of mercaptans, H₂S and CO₂Still a significant challenge, especially in view of the increasingly stringent environmental and technical requirements, and the driving force for the continued cost reduction of natural gas processing plants.

The removal of contaminants from gases, and to a lesser extent also organic liquids such as, for example, LPG streams, is typically accomplished by scrubbing the stream with an absorbent solution, typically at a relatively low temperature to facilitate the absorption of the contaminants. Most of the impurities are absorbed in the absorbent solution, and then the absorbent solution rich in (impurities) is sent to a regeneration step for regeneration. The lean absorbent solution from the regeneration step is then typically cooled and recycled to the absorption step. Typical absorbent solutions contain alkaline absorbents and amine compounds are preferred over other options (e.g., hot carbon)Potassium salt). Even more preferred are alkanolamines. A conventional absorbent is, for example, 2-hydroxyethylamine, also known as Monoethanolamine (MEA). According to a reversible exothermic reaction, the absorbed impurities react with the alkanolamine present in the solution. For MEA, two molecule MEA's are typically required to absorb one molecule of CO₂. More complex sterically hindered amines (including tertiary amines) have been found to provide improved stoichiometry.

These types of solvents chemically react with impurities to form the hot regenerating salt, and are generally referred to herein as chemical solvents. Alkanolamines derived from primary, secondary and/or tertiary amines are the most widely used chemical solvents. The most commonly used amines are derived from ethanolamines, especially Monoethanolamine (MEA), Diethanolamine (DEA), Triethanolamine (TEA), Diisopropanolamine (DIPA) and Methyldiethanolamine (MDEA). A disadvantage of such chemical solvents is that the chemical bonds between the solvent and the impurities need to be broken during the regeneration step, which requires a large amount of energy. In particular, the regeneration of primary and secondary alkanolamine solutions consumes large amounts of steam. Since thiols are weak acids, when H is present₂S and CO₂When the latter two react faster with alkanolamines, removal of the mercaptans by chemical solvents will not be efficient. Thus, mercaptans can chemically react with alkanolamines, but they react with H₂S and CO₂There is competition.

As an alternative to chemical solvents, so-called physical solvents are often used to capture small amounts of sulphur-containing components (such as mercaptans). Physical solvents rely on physical absorption processes, and impurities are dissolved and thus physically absorbed into the physical solvent. The energy associated with impurities is generally less than most typical so-called chemical solvents. Typical physical solvents are: mixtures of sulfolane and its derivatives, fatty acid amides, N-methyl-2-pyrrolidone (NMP), methanol, and dialkyl ethers of polyethylene glycol: (United Carbide corporation (Union Carbide)).

Mixtures of chemical and physical solvents, so-called complex solvents, may also be used. This complex solvent can achieve very low impurity levels in a single processing step by a combination of both removal of large amounts of impurities by physical solvents and rigorous purification by chemical solvents.

One well-known commercial complex solvent isSolvent(s)

Which are commonly used to treat refinery gases, natural gases and synthesis gases.The solvent is a mixture of sulfolane, alkanolamine (DIPA or MDEA) and water. When it is desired to completely remove H₂S and CO₂And the deep removal of COS is often selected as

A DIPA-containing solution of (a). Used in most sulfolane plants employed worldwide

A solvent. The solution containing MDEA is calledIs usually used in CO₂Selective removal of H in the presence of₂And S, and the COS can be partially removed. US4,085,192 describes selective removal of H₂S by using such a composition comprising an alkanolamine and sulfolaneType solvent. TheThe solvent shows p-H₂S、CO₂And good absorption capacity of mercaptans, however, it also shows co-absorption of valuable hydrocarbons. Against hydrocarbons should be avoidedCo-absorbing to reduce the loss of hydrocarbons in the separated impurities.

US2016/0288046a1 relates to a process for removing acidic sulfur components from a fluid stream by using an aqueous mixture of an amine component and a physical solvent. The amine component is typically a tertiary amine such as, in particular, 3-dimethylamino-1, 2-propanediol (DMAPD), 3-diethylaminopropane-1, 2-diol, 2-hydroxymethyl-2-dimethylaminopropane-1, 3-diol, or 2-hydroxymethyl-2-diethylaminopropane-1, 3-diol, and sterically hindered amines such as 2-hydroxymethyl-2-methylaminopropane-1, 3-diol, and 2-methyl-2-hydroxyethylaminopropanol. Preferred physical solvents include monofunctional and difunctional alcohols having a dielectric constant of less than about 20, such as: methoxy Triethylene Glycol (MTG), Methoxy Diethylene Glycol (MDG), ethoxy triethylene glycol, butoxy triethylene glycol, and mixtures thereof, or glycol ethers such as methyl terminated polyethylene glycol ethers and methyl terminated polypropylene glycols. US2016/0288046A1 relates primarily to the removal of acid sulfur components, and in particular to the selective removal of H from gas streams₂S, the gas stream containing other impurities, e.g. N₂、CO₂、CH₄、C₂H₆、C₃H₈、H₂、CO、H₂O、COS、HCN、NH₃、O₂And/or a thiol. In US2016/0288046a1, it was found that the dielectric properties of the amine component and the physical solvent are important. Most preferred are complex solvents having a low dielectric constant. No mention is made about the amount of co-absorption of hydrocarbons.

US8,313,718 discloses a method for removing H from a hydrocarbon gas stream also containing mercaptans by using an absorption (scrubbing) composition₂S and CO₂The absorption (scrubbing) composition comprises a solution (chemical or physical solvent, or mixtures thereof) and an effective amount of a thiol inclusion compound such as cyclodextrin, calixarene, cucurbituril, cryptand, or mixtures thereof. Alkanolamines are mentioned as chemical solvents and include, for example, Monoethanolamine (MEA), Diethanolamine (DEA), Triethanolamine (TEA), Diisopropylamine (DIPA), Diglycolamine (DGA) and Methyldiethanolamine (MDEA). The following are mentioned as useful physical solvents: cyclotetramethylene sulfone, fatty acid amide, N-alkylMixtures of pyrrolidone such as N-methyl pyrrolidone and the corresponding piperidones, methanol, and dialkyl ethers of polyethylene glycol. US8,313,718 demonstrates that the addition of such a thiol inclusion compound improves the removal of thiols. A significant disadvantage of the process of US8,313,718 is that it requires a composition with additional components on top of the conventional complex solvent, which in turn results in additional raw material costs. The co-absorption of hydrocarbons is not mentioned.

US5,413,627 discloses a process for the preparation of a catalyst in H₂、N₂、Ar、CO₂CO and aliphatic hydrocarbons using a physical detergent to selectively remove sulfur compounds, such as H₂S、COS、CS₂And mercaptans. Heterocyclic compounds are used as suitable physical detergents which need to have five or more ring atoms of which 2 are heteroatoms, one is nitrogen and the other is oxygen or nitrogen. The nitrogen atoms present in the ring are double-or single-bonded, but if single-bonded, the nitrogen is organically substituted. Various detergents are disclosed. The physical detergent may also be used in the form of a physically active detergent composition together with a compound selected from various heterocycles. US5,412,627 relates primarily to CO₂In the presence of sulfur-removing compounds (e.g. H)₂S) without involving an efficient simultaneous removal of mercaptans. The co-absorption of hydrocarbons is not mentioned.

US2009/0299122a1 proposes a process for producing purified hydrocarbon gas which does not result in a significant risk of loss of hydrocarbon product. First, the gas stream is partially purified by cooling the gas stream and removing any solidified and/or liquefied impurities. The partially purified gas is then compressed and the compressed partially purified gas is further contacted with an absorption liquid. The absorption liquid may comprise an amine compound, such as an alkanolamine, and may further comprise a physical solvent. According to US2009/0299122a1, suitable physical solvents include: tetramethylene sulfone and derivatives, amides of aliphatic carboxylic acids, N-alkylpyrrolidones, in particular N-methylpyrrolidone, N-alkylpiperidinones, in particular N-methylpiperidinone, methanol, ethanol, ethylene glycol, polyethylene glycol, mono-or di- (C) of ethylene glycol or polyethylene glycol₁-C₄) An alkyl ether. It should be mentioned that US2009/0299122a1 does not describe any feasible example. Thus, US2009/0299122a1 does not provide any experimental evidence-demonstrating effective simultaneous removal of mercaptans and other impurities (such as H)₂S and CO₂) And reduces the risk of significant loss of hydrocarbon products.

In the prior art, the solvent N-methyl-2-pyrrolidone (NMP) is generally recommended as a physical solvent. However, NMP is under supervision due to concerns about its potential health effects. NMP has attracted increasing attention because environmental regulatory bodies (first in california, and more recently in the european union) have sought to exercise control over such solvents-first in markets where it presents an inhalation hazard. Furthermore, NMP is currently known to cause reproductive toxicity (which is considered to be reproductive toxic), and from 12/1/2010 it is labeled as "reproductive toxicity category 2" in the EU. Formulations containing > 0.3% NMP must be so labeled. Thus, the use of solvents is limited to professional users. NMP has been placed on the REACH list of "substances of great interest" (SVHC) and is expected to be placed under authorization or restriction sooner or later.

Thus, there remains a need for less toxic, more economical and more environmentally friendly absorbent solutions that are capable of retaining other impurities (e.g., H)₂S and CO₂) In the presence of these, mercaptans are absorbed efficiently while maintaining excellent performance in conventional absorption-regeneration cycles, and they also exhibit negligible hydrocarbon co-absorption.

Disclosure of Invention

The inventors have now surprisingly found that it is possible to provide an improved process which meets the above-mentioned needs.

The invention provides a method, comprising:

step a) contacting a feed stream comprising an impurity with an absorbent stream in a counter stream to produce an impurity-depleted product stream that is depleted in molar mass of the impurity relative to the molar mass of the impurity in the feed stream and an impurity-enriched absorbent stream that is enriched in molar mass of the impurity relative to the molar mass of the impurity in the absorbent stream;

step b) treating the impurity-enriched absorbent stream to form a gas stream comprising the impurity and a regenerated absorbent stream that is depleted in molar amount of the impurity relative to the molar amount of the impurity in the impurity-enriched absorbent stream;

wherein the absorbent stream comprises:

i. at least 15 weight percent (hereinafter wt%) of at least one substituted 2-pyrrolidone of the general formula (I) [ hereinafter compound (a) ], relative to the total weight of the absorbent stream:

wherein:

-R₁and R₂Each of which, equal to or different from each other, and at each occurrence, is independently selected from H or CH₃；

-each R is the same or different from each other and, at each occurrence, is selected from H or CH₃；

-i is an integer ranging from 0 to 3;

-o is an integer ranging from 2 to 6; n is an integer ranging from 0 to 4; m is an integer ranging from 0 to 4;

alternatively, the first and second electrodes may be,

a mixture [ hereinafter mixture (M) ] comprising at least one substituted 2-pyrrolidone of formula (II) herein below [ hereinafter compound (B) ] and at least one amine compound of formula (III) herein below [ hereinafter compound (C) ]:

wherein:

-each R' is the same or different from each other and, at each occurrence, is independently selected from H or CH₃

-j is an integer ranging from 0 to 3

-R₃、R₄、R₅And R₆Each of which, equal to or different from each other, and at each occurrence, is independently selected from H or CH₃；

-q is an integer ranging from 0 to 1; p is an integer ranging from 1 to 6; with the proviso that when p is 1 and q is 0, then R₃And R₄Is CH₃When p + q is 2, then R₃、R₄、R₅Or R₆Is CH₃；

-R₇、R₈And R₉Each of which, equal to or different from each other, and at each occurrence, is independently selected from H, C_1-10Alkyl radical, C_1-10Alkoxy alcohols or C_1-10An alkanol group; with the proviso that R₇、R₈Or R₉At least one of which is C_1-10Alkoxy alcohols or C_1-10And (3) alkanol groups.

The invention also provides a composition comprising the mixture (M).

Drawings

Fig. 1 shows a schematic view of an apparatus suitable for removing impurities from a gas stream.

Detailed Description

The present invention will be described with respect to particular embodiments and with reference to certain drawings but the invention is not limited thereto but only by the claims. Any drawings described are only schematic and are non-limiting. In the drawings, the size of some of the elements may be exaggerated and not drawn on scale for illustrative purposes. The dimensions and relative dimensions do not necessarily correspond to actual reductions to practice of the invention.

Furthermore, the terms first, second, third and the like in the description and in the claims, are used for distinguishing between similar elements and not necessarily for describing a sequential or chronological order. The terms so used are interchangeable under appropriate circumstances and the embodiments of the invention can operate in other sequences than described or illustrated herein.

Furthermore, the terms top, bottom, over, under and the like in the description and the claims are used for descriptive purposes and not necessarily for describing relative positions. The terms so used are interchangeable under appropriate circumstances and the embodiments of the invention described herein are capable of operation in other orientations than described or illustrated herein.

The term "comprising" as used in the claims should not be construed as being limited to the means listed thereafter; without excluding other elements or steps. It needs to be interpreted as: it is specifically intended that the present features, integers, steps or components as referred to are present but does not preclude the presence or addition of one or more other features, integers, steps or components or groups thereof. Thus, the scope of the expression "a device comprising means a and B" should not be limited to devices consisting of only components a and B. This means that only the devices are a and B with respect to the relevant components of the invention. Thus, the terms "comprising" and "including" encompass the more limiting terms "consisting essentially of …" and "consisting of …".

As used above and below, the following definitions apply unless otherwise indicated.

The term "alkyl", alone or in combination, refers to an alkane-derived group, e.g., C_F-GAlkyl is defined as a straight-chain or branched alkyl group having F to G carbon atoms, e.g. C_1-4Alkyl is defined as a straight-chain or branched alkyl group having 1 to 4 carbon atoms, such as, for example, methyl, ethyl, 1-propyl, 2-propyl, 1-butyl, 2-methyl-2-propyl, 2-methyl-1-propyl. The alkyl group may be a straight chain alkyl group or a branched alkyl group.

The term "alkanol", alone or in combination, refers to any alkyl group containing one or more hydroxyl (-OH) functional groups, e.g., C_F-GAlkanols are defined as straight-chain or branched alkanols having F to G carbon atoms, e.g. C_1-4Alkanols are defined as straight-chain or branched alkanols having from 1 to 4 carbon atoms. The alkanol group may be mono-, di-, tri-or poly-valent and may be a linear alkanol or a branched alkanol.

The term "alkoxyalcohol", alone or in combination, means an organic compound of formula X-O-Y, wherein X is alkyl substituted by-O-Y, which is substituted with-O-YWherein Y is an alkanol group. E.g. C_F-GAlkoxyalcohols are defined as alkoxyalcohols having a total of F-G carbon atoms, e.g. C_1-4Alkoxylated alcohols are defined as alkoxylated alcohol groups having from 1 to 4 carbon atoms, such as, for example, ethoxyethanol, methoxyethanol, ethoxymethanol, methoxymethanol.

The term "alkanolamine" refers to an amine compound comprising at least one alkanol group, wherein the additional substituents are selected from H, alkyl groups or alkanol groups. In this context, a primary alkanolamine comprises one alkanol group and two hydrogens bonded to a nitrogen atom, a secondary alkanolamine comprises at least one alkanol group and at least one hydrogen bonded to a nitrogen atom, and a tertiary alkanolamine comprises at least one alkanol group and no hydrogen bonded to a nitrogen atom.

The term "at least one substituted 2-pyrrolidone of formula (I)" is intended to denote one or more than one substituted 2-pyrrolidone of formula (I). Mixtures of substituted 2-pyrrolidones of the general formula (I) can also be used for the purposes of the present invention. The term "at least one substituted 2-pyrrolidone of formula (II)" is intended to denote one or more than one substituted 2-pyrrolidone of formula (II). Mixtures of substituted 2-pyrrolidones of the general formula (II) can also be used for the purposes of the present invention. The term "at least one amine compound of formula (III)" is intended to denote one or more than one amine compound of formula (III). Mixtures of amine compounds of the general formula (III) can also be used for the purposes of the present invention.

It should be understood that the term "amount" relates to a characteristic that is measurable in terms of quantity. The term "amount" may denote a mass, or a weight, or a mole, or any physical or in any case numerical parameter, which is capable of indicating the presence of an impurity or a mixture of impurities at least at the level of an amount, unless otherwise stated.

In the context of the present invention, the expression "contacting a feed stream comprising impurities with an absorbent stream in counter-current" is intended to mean that the absorbent stream is contacted with the feed stream comprising impurities in such a way that: such that the absorbent stream and the feed stream approach each other in opposite directions. It should also be understood that the angle at which the streams approach each other may deviate by 180 °.

In the context of the present invention, at least one of the streams is a mobile stream. Thus, at least the following three cases may occur: contacting a static feed stream with a moving flowing absorbent stream; contacting the moving flowing feed stream with a static absorbent stream; or contacting the moving flowing feed stream with a moving flowing absorbent stream. The term "at least one of the streams" is intended to mean one or more than one stream.

As mentioned above, in the prior art, the solvent N-methyl-2-pyrrolidone (NMP) is generally recommended as a physical solvent. Applicants have now found that only specific substituted 2-pyrrolidones of formula (I) and formula (II) as detailed above, characterized by particular specific choices for o, n and m in formula (I) as defined above, and p and q in formula (II), can provide an absorbent stream that removes mercaptans from the feed stream more efficiently than NMP, as demonstrated by the examples below.

Applicants believe that in terms of chemical structure, extending the chain attached to the nitrogen of the substituted 2-pyrrolidone (formula (I) or formula (II) according to the present invention) to a total of at least four carbon atoms appears to produce an absorbent stream that is more effective in removing mercaptans from the feed stream. As a further advantage, compounds with extended chain lengths (such as N-N-butyl-2-pyrrolidone) have been found to be non-reprotoxic.

The applicant has also found that the specific choice of o, n and m in formula (I) and p and q in formula (II) also limits the chain length of the chain attached to the nitrogen of the substituted 2-pyrrolidone (formula (I) or formula (II) according to the invention) in terms of chemical structure, as defined above, and appears to produce an absorbent stream that maintains a low hydrocarbon co-absorption tendency. This brings the advantage that less valuable hydrocarbon compounds are lost in the separated impurities, and also leads to a higher process selectivity for the impurities.

In a preferred embodiment of the process according to the invention, in the compound (a) of formula (I), I is an integer ranging from 0 to 1, more preferably, in the compound (a) of formula (I), I is 0.

In accordance with the inventionIn a preferred embodiment of the process, in the compound (A) of the formula (I), R₁And R₂Each is H.

In a preferred embodiment of the process according to the invention, in compound (a) of general formula (I), o is an integer ranging from 2 to 5, more preferably o is an integer ranging from 2 to 4, even more preferably o is an integer selected from 2 or 3.

In a preferred embodiment of the process according to the invention, in the compound (a) of formula (I), n is an integer ranging from 0 to 3, more preferably n is an integer ranging from 0 to 2, even more preferably n is an integer selected from 0 or 1, most preferably in the compound (a) of formula (I), n is 0.

In a preferred embodiment of the process according to the invention, in the compound (a) of formula (I), m is an integer ranging from 0 to 3, more preferably m is an integer ranging from 0 to 2, even more preferably m is an integer selected from 0 or 1, most preferably in the compound (a) of formula (I), m is 0.

In a preferred embodiment of the process according to the invention, in the compound (B) of formula (II), j is an integer ranging from 0 to 1, more preferably, in the compound (B) of formula (II), j is 0.

In one embodiment of the process according to the invention, R in the compound (B) of the general formula (II)₅And R₆Each H, R in the compound (B) of the general formula (II)₃And R₄Each of which is the same or different from each other and, at each occurrence, is independently selected from H or CH₃Q is 1 and p is an integer ranging from 1 to 6; with the proviso that when p + q is 2, then R₃、R₄、R₅Or R₆At least one of them being CH₃。

In a preferred embodiment of the process according to the invention, R in the compound (B) of the general formula (II)₃、R₄、R₅And R₆Each is H, q is 1, and p is an integer in the range of 2 to 6.

In a more preferred embodiment of the process according to the invention, R in the compound (B) of the general formula (II)₃、R₄、R₅And R₆Each is H, q is 1, p is 2, 3 or 4, more preferably, p is 2.

In one embodiment of the process according to the invention, R in the compound (C) of the general formula (III)₇、R₈And R₉Each independently selected from H, C_1-5Alkyl radical, C_1-5Alkoxy alcohols or C_1-5An alkanol group; with the proviso that R₇、R₈Or R₉At least one of which is C_1-5Alkoxy alcohols or C_1-5And (3) alkanol groups.

In another embodiment of the process according to the invention, R in the compound (C) of the general formula (III)₇、R₈And R₉Each independently selected from H, C_1-5Alkyl or C_1-5An alkanol group; with the proviso that R₇、R₈Or R₉At least two of (a) are C_1-5And (3) alkanol groups.

In yet a further embodiment of the process according to the invention, R in the compound (C) of the general formula (III)₇、R₈And R₉Each independently selected from C_1-5Alkyl or C_1-5An alkanol group; with the proviso that R₇、R₈Or R₉At least one of which is C_1-5And (3) alkanol groups.

In a preferred embodiment of the process according to the invention, R in the compound (C) of the general formula (III)₇And R₈Each is C_1-5Alkanol group, R₉Is selected from C_1-5Alkyl or C_1-5And (3) alkanol groups.

In a more preferred embodiment of the process according to the invention, R in the compound (C) of the general formula (III)₇And R₈Each is C_1-5Alkanol group, R₉Is C_1-5An alkyl group. More preferably, R₇And R₈Each is C_1-4Alkanol group, R₉Is C_1-4An alkyl group. Even more preferably, R₇And R₈Each is C_1-3Alkanol group, R₉Is C_1-3An alkyl group.

In the compounds (a) of the absorbent stream used in step a) of the process according to the invention, preferably R₁And R₂Is H, i is 0. Thus, preferred compounds (A) are selected from those of the following formula (I-a) herein:

wherein:

-o is an integer ranging from 2 to 4; n is an integer selected from 0 or 1; m is an integer selected from 0 or 1.

Typical compounds (a) suitable for step a) of the process of the invention may include, but are not limited to: dimethylaminopropyl-2-pyrrolidone (DMAP-2-pyrrolidone), dimethylaminoethyl-2-pyrrolidone (DMAE-2-pyrrolidone), diethylaminopropyl-2-pyrrolidone (DEAP-2-pyrrolidone), or a mixture of two or more thereof.

More preferably, in compound (a), which is comprised in the absorbent stream used in step a) of the process according to the invention, o is an integer ranging from 2 to 4; n is 0 and m is 0. Thus, more preferred compounds (A) are selected from those of the following formula (I-b) herein:

wherein:

-o is an integer ranging from 2 to 4.

According to a preferred embodiment of the process of the invention, compound (A) is selected from those of formula (I-c) or formula (I-d) herein below:

the inventors have found that compound (a), as detailed herein, which is comprised in the absorbent stream according to step a) of the process of the present invention, can act as both a physical solvent and a chemical solvent, thereby forming a so-called composite solvent on its own. Without being bound by this theory, the inventors believe that the pyrrolidone ring in compound (A) provides enhanced ability to dissolve thiols, while the tertiary amine substitution on the pyrrolidone ring in compound (A) is providedThe radicals may be associated with other impurities (e.g. CO)₂And H₂S) reacting.

The inventors have also found that in other impurities (e.g. H)₂S and CO₂) When compound (a) is used in the absorbent stream, a minimum amount of 15 wt% of compound (a) relative to the total weight of the absorbent stream is required to achieve effective mercaptan removal.

In the compounds (B) which are comprised in the mixture (M) used in step a) of the process according to the invention, preferably R₅And R₆Is H, j is 0. Preferred compounds (B) are therefore those selected from the following formulae (II-a) herein:

wherein:

-R₃and R₄Each of which is independently selected from H or CH₃；

q is 1; p is an integer in the range of 2 to 6.

Typical compounds (B) suitable for step a) of the process of the invention may therefore include, but are not limited to, specific N-alkyl-2-pyrrolidones, such as: N-N-butyl-2-pyrrolidone, N-sec-butyl-2-pyrrolidone, N-isobutyl-2-pyrrolidone, N-tert-butyl-2-pyrrolidone, N-N-pentyl-2-pyrrolidone, N-sec-pentyl-2-pyrrolidone, N-tert-pentyl-2-pyrrolidone, n-3-pentyl-2-pyrrolidone, N-isopentyl-2-pyrrolidone, N-neopentyl-2-pyrrolidone, N-N-hexyl-2-pyrrolidone, N-N-heptyl-2-pyrrolidone, N-N-octyl-2-pyrrolidone, or a mixture of two or more thereof.

The inventors found that, in terms of chemical structure, in the compound (B) used in step a) according to the invention, extending the carbon chain attached to the nitrogen of the pyrrolidone ring to at least four carbon atoms, an absorbent stream is obtained: mercaptans are removed from the feed stream more efficiently than NMP, as demonstrated in the examples below, and are anogenital toxic. The inventors have also found that compounds (B) according to the invention, in which the carbon chain attached to the nitrogen of the pyrrolidone ring is limited to at most 8 carbon atoms, maintain a low tendency to hydrocarbon co-absorption.

More preferably, in the compound (B) comprised in the mixture (M) used in step a) of the process according to the invention, R₃、R₄、R₅And R₆Is H, j is 0,. Thus, more preferred compounds (B) are those selected from the following formulae (II-B) herein:

wherein:

-p is an integer ranging from 2 to 6.

According to one embodiment of the process according to the invention, the compound (B) is selected from those of formulae (II-c) to (II-g) herein below:

according to a preferred embodiment of the process according to the invention, the compound (B) is selected from those of formulae (II-c) to (II-e) as detailed above.

According to a more preferred embodiment, compound (B) in the absorbent stream used in step a) of the process according to the invention is a compound of formula (II-c):

in the compounds (C) which are contained in the mixture (M) used in step a) of the process according to the invention, preferably R₇、R₈And R₉Each independently selected from H, C_1-4Alkyl radical, C_1-4Alkoxy alcohols or C_1-4An alkanol group; with the proviso that R₇、R₈Or R₉At least one of which is C_1-4Alkoxy alcohols, or C_1-3And (3) alkanol groups.

Typical compounds (C) suitable for use in step a) of the process of the present invention may include primary, secondary and tertiary alkanolamines such as, but not limited to: monoethanolamine (MEA), Diethanolamine (DEA), Triethanolamine (TEA), Monomethyl Monoethanolamine (MMEA), diethyl monoethanolamine (edmea), Diisopropanolamine (DIPA), Diglycolamine (DGA) and Methyldiethanolamine (MDEA), or mixtures of two or more thereof.

Preferably, the compound (C), which is comprised in the mixture (M) used in step a) of the process of the present invention, is selected from tertiary alkanolamines, such as, in particular: triethanolamine (TEA), diethylmonoethanolamine, and Methyldiethanolamine (MDEA). More preferably, compound (C), which is comprised in the absorbent stream used in step a) of the process of the present invention, is Methyldiethanolamine (MDEA).

The inventors have found that even in the presence of compound (B), and comprised in the mixture (M) used in step a) of the process according to the invention, the tertiary alkanolamine forms little irreversible components with impurities. Furthermore, the tertiary alkanolamine contained in mixture (M) brings the following advantages: under typical operating conditions, they will be more thermally and chemically stable, and generally they require less energy to regenerate.

In certain embodiments, compound (C), which is comprised in the mixture (M) used in step a) of the process according to the invention, is Diglycolamine (DGA).

A non-limiting example of a commercially available tertiary alkanolamine is100 available from eastman chemical Company.

It is also understood that all definitions and preferences described above for compound (a) and compound (C) apply equally to this and all other examples, as described below.

As mentioned above, the absorbent stream in step a) of the process according to the invention comprises at least 15% by weight, relative to the total weight of the absorbent stream, of at least one compound (a) of general formula (I) as detailed above.

Advantageously, the weight percentage of compound (a) contained in the absorbent stream used in step a) with respect to the total weight of the absorbent stream is: equal to or greater than 20 wt%, preferably equal to or greater than 25 wt%, preferably equal to or greater than 30 wt%, preferably equal to or greater than 35 wt%, preferably equal to or greater than 40 wt%, preferably equal to or greater than 45 wt%, preferably equal to or greater than 50 wt%, preferably equal to or greater than 55 wt%, preferably equal to or greater than 60 wt%, preferably equal to or greater than 65 wt%, preferably equal to or greater than 70 wt%, preferably equal to or greater than 75 wt%, preferably equal to or greater than 80 wt%, preferably equal to or greater than 85 wt%, preferably equal to or greater than 90 wt%, preferably equal to or greater than 95 wt%, preferably equal to or greater than 98 wt%.

It is also understood that the upper limit value of the weight percentage of compound (a) (comprised in the absorbent stream used in step a) with respect to the total weight of the absorbent stream is not particularly limited, but is advantageously equal to or less than 99 wt%, preferably equal to or less than 95 wt%, preferably equal to or less than 90 wt%, preferably equal to or less than 85 wt%.

As described above, the inventors found that the compound (a) can function as both a physical solvent and a chemical solvent. Thus, compound (a) may be used as a solvent, as part of the absorbent stream or as the absorbent stream itself.

In an embodiment, as detailed above, the absorbent stream in step a) of the process according to the invention consists essentially of compound (a) of general formula (I).

For the purposes of the present invention, the expression "consisting essentially of …" is intended to indicate that any additional components are present in an amount of at most 5 wt%, preferably at most 2 wt%, relative to the total weight of the absorbent stream. For example, any additional component other than compound (a) as detailed above is present in an amount of at most 5 wt%, preferably at most 2 wt%, relative to the total weight of the absorbent stream.

The inventors also found that good results were also obtained when compound (a) detailed above was further mixed with compound (C) of general formula (III) detailed above.

According to a preferred embodiment, the absorbent stream in step a) of the process according to the invention comprises at least 15 wt% of at least one compound (a) of general formula (I) as detailed above, relative to the total weight of the absorbent stream, and further comprises at least one compound (C) of general formula (III) as detailed above.

Advantageously, at least one amine compound (C) of general formula (III) is contained in the absorbent stream in an amount corresponding to the following weight ratio, wherein the weight ratio of compound (C) to compound (a) is: at least 0.5:1, preferably at least 0.75:1, more preferably at least 1:1, even more preferably at least 1.5:1, still even more preferably at least 1.75: 1. It will also be appreciated that the weight ratio of compound (C) to compound (a) in the absorbent stream is generally at most 5:1, preferably at most 4:1, more preferably at most 3.5:1, more preferably at most 3:1, more preferably at most 2.5: 1.

According to certain embodiments of the present invention, the absorbent stream used in step a) of the process of the present invention may further comprise water.

When water is present in the absorbent stream, then water is present in the absorbent stream in the following amounts relative to the total amount of all components of the absorbent stream: at least 0.5 wt%, preferably at least 5 wt%, preferably at least 10 wt%, more preferably at least 15 wt%, even more preferably at least 20 wt%, and even more preferably at least 22 wt%.

It is also understood that water is present in the absorbent stream in the following amounts relative to the total amount of all components of the absorbent stream: up to 85 wt%, preferably up to 70 wt%, more preferably up to 60 wt%, even more preferably up to 50 wt%, more preferably up to 40 wt%, even more preferably up to 30 wt%, more preferably up to 28 wt%.

According to a more preferred embodiment, the absorbent stream in step a) of the process according to the invention comprises a composition [ hereinafter composition (C) ] comprising: at least 15% by weight of at least one compound (a) of general formula (I) as detailed above, relative to the total weight of composition (C), at least one compound (C) of general formula (III) as detailed above, and water.

Advantageously, the amount of water contained in composition (C) corresponds to the weight ratio of water to compound (a) being: at least 0.25:1, preferably at least 0.3:1, more preferably at least 0.4:1, even more preferably at least 0.6:1, and yet even more preferably at least 0.9: 1. It will also be appreciated that the weight ratio of water to compound (a) in composition (C) is generally at most 4:1, preferably at most 3:1, more preferably at most 2.5:1, even more preferably at most 2:1, even more preferably at most 1.5:1, even more preferably at most 1.1: 1.

Advantageously, the weight percentage of compound (a), which is contained in composition (C) used in step a), with respect to the total weight of composition (C), is: advantageously equal to or greater than 18% by weight, preferably equal to or greater than 20% by weight, more preferably equal to or greater than 21% by weight, even more preferably equal to or greater than 22% by weight.

It is also understood that the upper limit value of the weight percentage of compound (a) which is contained in composition (C) used in step a) with respect to the total weight of composition (C) is not particularly limited, but is advantageously equal to or less than 50 wt%, preferably equal to or less than 40 wt%, more preferably equal to or less than 35 wt%, even more preferably equal to or less than 30 wt%, even more preferably equal to or less than 29 wt%, most preferably equal to or less than 28 wt%.

Advantageously, the weight percentage of compound (C), which is contained in composition (C) used in step a), with respect to the total weight of composition (C), is: advantageously equal to or greater than 2 wt%, preferably equal to or greater than 5 wt%, preferably equal to or greater than 10 wt%, more preferably equal to or greater than 20 wt%, even more preferably equal to or greater than 30 wt%, yet even more preferably equal to or greater than 40 wt%, most preferably equal to or greater than 45 wt%.

It is also understood that the upper limit value of the percentage by weight of compound (C) which is contained in composition (C) used in step a) with respect to the total weight of composition (C) is: advantageously equal to or less than 85% by weight, preferably equal to or less than 80% by weight, more preferably equal to or less than 75% by weight, more preferably equal to or less than 70% by weight, more preferably equal to or less than 65% by weight, even more preferably equal to or less than 60% by weight, still even more preferably equal to or less than 55% by weight.

It is also understood that all definitions and preferences described above for compound (B) and compound (C) apply equally to this and all other examples, as described below.

As mentioned above, the absorbent stream in step a) of the process according to the invention may comprise the mixture (M) -as detailed above.

According to an embodiment of the process according to the invention, at least one compound (B) of general formula (II) is advantageously contained in the mixture (M) in an amount corresponding to the weight ratio of compound (B) to compound (C): at least 0.05:1, preferably at least 0.1:1, more preferably at least 0.2:1, more preferably at least 0.3:1, more preferably at least 0.35:1, even more preferably at least 0.4:1, and yet even more preferably at least 0.45: 1. It will also be appreciated that the weight ratio of compound (C) to compound (a) in mixture (M) is generally: at most 2:1, preferably at most 1.5:1, more preferably at most 1:1, more preferably at most 0.75:1, even more preferably at most 0.65:1, yet even more preferably at most 0.55: 1.

In a preferred embodiment of the process according to the invention, the weight percentage of compound (B), which is contained in mixture (M) used in step a), with respect to the total weight of mixture (M), is: advantageously equal to or greater than 5 wt%, preferably equal to or greater than 10 wt%, more preferably equal to or greater than 15 wt%, more preferably equal to or greater than 18 wt%, more preferably equal to or greater than 20 wt%, even more preferably equal to or greater than 22 wt%, and yet even more preferably equal to or greater than 25 wt%.

It is also understood that the upper limit value of the percentage by weight of compound (B) which is contained in mixture (M) used in step a) with respect to the total weight of mixture (M) is: advantageously equal to or less than 50 wt%, preferably equal to or less than 45 wt%, more preferably equal to or less than 40 wt%, more preferably equal to or less than 35 wt%, more preferably equal to or less than 30 wt%, even more preferably equal to or less than 29 wt%, most preferably equal to or less than 28 wt%.

In a preferred embodiment of the process according to the invention, the weight percentage of compound (C) contained in mixture (M) used in step a) with respect to the total weight of mixture (M) is: advantageously equal to or greater than 2 wt%, preferably equal to or greater than 5 wt%, preferably equal to or greater than 10 wt%, more preferably equal to or greater than 20 wt%, even more preferably equal to or greater than 30 wt%, yet even more preferably equal to or greater than 40 wt%, most preferably equal to or greater than 45 wt%.

It is also understood that the upper limit value of the percentage by weight of compound (C) contained in the mixture (M) used in step a) with respect to the total weight of the mixture (M) is: advantageously equal to or less than 85% by weight, preferably equal to or less than 80% by weight, more preferably equal to or less than 75% by weight, more preferably equal to or less than 70% by weight, more preferably equal to or less than 65% by weight, even more preferably equal to or less than 60% by weight, still even more preferably equal to or less than 55% by weight.

According to an embodiment, the absorbent stream used in step a) of the process according to the invention consists essentially of:

-from 15% to 40% by weight of at least one compound (A) of general formula (II) as defined above,

-from 30% to 65% by weight of at least one compound (C) of general formula (III) as defined above,

-from 15% to 40% by weight of water,

all wt% are relative to the total weight of the absorbent stream.

It is also understood that in this example, any additional ingredients, other than compound (a) as detailed above, compound (C) as detailed above and water, are present in an amount of at most 5 wt%, preferably at most 2 wt%, relative to the total weight of the absorbent stream.

Preferably, the mixture (M) used in step a) of the process according to the invention also comprises water.

In this preferred embodiment of the process according to the invention, the weight percentage of compound (B) contained in mixture (M) used in step a) with respect to the total weight of mixture (M) is: advantageously equal to or greater than 5% by weight, preferably equal to or greater than 10% by weight, more preferably equal to or greater than 15% by weight, more preferably equal to or greater than 18% by weight, more preferably equal to or greater than 20% by weight, and even more preferably equal to or greater than 22% by weight.

It is also understood that the upper limit value of the percentage by weight of compound (B) contained in mixture (M) used in step a) with respect to the total weight of mixture (M) is: advantageously equal to or less than 50% by weight, preferably equal to or less than 45% by weight, more preferably equal to or less than 40% by weight, more preferably equal to or less than 35% by weight, more preferably equal to or less than 30% by weight, even more preferably equal to or less than 28% by weight.

In a preferred embodiment of the process according to the invention, the weight percentages of compound (C) contained in the mixture (M) used in step a), with respect to the total weight of the mixture (M), are: advantageously equal to or greater than 2 wt%, preferably equal to or greater than 5 wt%, preferably equal to or greater than 10 wt%, more preferably equal to or greater than 20 wt%, even more preferably equal to or greater than 30 wt%, yet even more preferably equal to or greater than 40 wt%, most preferably equal to or greater than 45 wt%.

It is also understood that the upper limit value of the percentage by weight of compound (C) contained in the mixture (M) used in step a) with respect to the total weight of the mixture (M) is: advantageously equal to or less than 70% by weight, preferably equal to or less than 65% by weight, more preferably equal to or less than 60% by weight, even more preferably equal to or less than 55% by weight.

According to an embodiment of the method according to the invention, water is generally added to the mixture (M) in the following amounts (corresponding to the weight ratio of water to compound (B)): at least 0.25:1, preferably at least 0.3:1, more preferably at least 0.4:1, even more preferably at least 0.6:1, yet even more preferably at least 0.9: 1. It will also be appreciated that the weight ratio of water to compound (B) in the absorbent stream is typically: at most 4:1, preferably at most 3:1, more preferably at most 2.5:1, even more preferably at most 2:1, yet even more preferably at most 1.1: 1.

Good results were obtained when: the weight percentage of compound (B) contained in mixture (M) used in step a) is comprised between 10 and 35% by weight with respect to the total weight of mixture (M); the weight percentage of compound (C) contained in mixture (M) used in step a) is between 30 and 65% by weight with respect to the total weight of mixture (M); the weight percentage of water (contained in the mixture (M) used in step a) is between 15 and 40% by weight with respect to the total weight of the mixture (M).

According to a preferred embodiment, the absorbent stream used in step a) of the process according to the invention comprises:

-from 10% to 35% by weight of at least one compound (B) of general formula (II) as defined above,

-from 30% to 65% by weight of at least one compound (C) of general formula (III) as defined above,

-from 15% to 40% by weight of water,

all wt% are relative to the total weight of the absorbent stream.

According to another embodiment, the absorbent stream used in step a) of the process according to the invention consists essentially of:

-from 10% to 35% by weight of at least one compound (B) of general formula (II) as defined above,

-from 30% to 65% by weight of at least one compound (C) of general formula (III) as defined above,

-from 15% to 40% by weight of water,

all wt% are relative to the total weight of the absorbent stream.

It is also understood that in this example, any additional ingredients (other than compound (B) as detailed above, compound (C) as detailed above and water) are present in an amount of at most 5 wt%, preferably at most 2 wt%, relative to the total weight of the absorbent stream.

If desired, the absorbent stream may further comprise a promoter for the reaction of the absorbent stream with at least one impurity, in particular with carbon dioxide. The promoter provides a significant improvement in the system kinetics, faster absorption rates, higher loading, lower absorbent/feed stream ratios, smaller plant designs, and lower regeneration heat requirements, and thus lower cooling capacity. A lower absorbent stream/feed stream ratio may lead to a more compact design of the plant (plant), absorber and regenerator. Alternatively, when the same absorbent stream/feed stream ratio is used, a substantially greater amount of impurities can generally be removed.

Advantageously, the weight percentages of promoter (comprised in the absorbent stream used in step a) relative to the total weight of the absorbent stream are: 0.1 to 20 wt.%, preferably at least 0.5 wt.%, preferably at least 1 wt.%, preferably at least 1.5 wt.%, preferably at least 2 wt.%, preferably at least 2.5 wt.%; and, alternatively, or in combination therewith, up to 18 wt%, preferably up to 16 wt%, preferably up to 14 wt%, preferably up to 12 wt%, preferably up to 10 wt%, preferably up to 9 wt%, even more preferably up to 8.5 wt% by weight.

Typical promoters, suitable for use in the absorbent stream used in step a) of the process of the present invention, may thus include, but are not limited to: amines, alcohols, ketones, vinyl alcohols, vinyl ketones, ether alcohols, ether ketones, glycols, polyethylene glycols, polypropylene glycols, ethylene glycol propylene glycol copolymers, glycol ethers, mercapto glycols, thiols, sulfones, sulfoxides, N-alkylated 2-pyrrolidones, N-alkylated piperidones, cyclotetramethylene sulfones, N-alkyl formamides, N-alkyl acetamides, alkyl phosphates, alkylene carbonates and/or dialkyl carbonates. More preferred candidates are Monoethanolamine (MEA), Diethanolamine (DEA), monomethylethanolamine (MMEA), piperazine, 2-methylpiperazine, N-ethylpiperazine, N-Hydroxyethylpiperazine (HEP), N- (2-aminoethyl) piperazine, homopiperazine, piperidine and morpholine. Most preferred as promoter is piperazine.

Typically, the feed stream comprises at least one impurity selected from mercaptans, hydrogen sulfide (H)₂S), carbon dioxide (CO)₂) Carbon Oxysulfide (COS), carbon disulfide (CS)₂) And disulfides.

In particular, the feed stream comprises mercaptans and at least one other impurity selected from H₂S、CO₂、COS、CS₂And disulfides.

We have found that even in the presence of other impurities (e.g., H)₂S and CO₂) Mercaptans, in the presence, can also be effectively removed from the feed stream. The inventors have found that the compound (B) specified herein can act as a physical solvent, while the compound (C) specified herein can act as a chemical solvent, forming a so-called complex solvent. The inventors believe that the pyrrolidone ring in compound (B) provides an improved ability to solubilize thiols while amine compound (C) is capable of reacting with other impurities (e.g., H)₂S and CO₂) And (4) reacting. Alternatively, the compounds (A) specified herein may act simultaneouslyA physical solvent and a chemical solvent, thereby forming a so-called composite solvent alone. The inventors believe that the pyrrolidone ring in compound (A) provides an increased ability to solubilize thiols, while the tertiary amine substituent on the pyrrolidone ring in compound (A) may be associated with other impurities (e.g. H)₂S and CO₂) And (4) reacting.

It will be appreciated that in step a), the molar amount of impurities in the impurity-depleted product stream is reduced relative to the molar amount of impurities in the feed stream. In addition, the molar amount of impurities in the enriched absorbent stream is increased relative to the molar amount of impurities in the absorbent stream.

The molar amount of impurities in the impurity-depleted product stream is reduced by at least 5%, preferably at least 10%, more preferably at least 20%, even more preferably at least 30%, yet even more preferably at least 40%, most preferably at least 50% relative to the molar amount of impurities in the feed stream.

The molar amount of impurities in the enriched absorbent stream is increased by at least 5%, preferably at least 10%, more preferably at least 20%, even more preferably at least 30%, still even more preferably at least 40%, most preferably at least 50% relative to the molar amount of impurities in the absorbent stream.

The molar amount of mercaptans in the impurity-depleted product stream is reduced by at least 5%, preferably at least 10%, more preferably at least 20%, even more preferably at least 30%, yet even more preferably at least 40%, most preferably at least 50% relative to the molar amount of mercaptans in the feed stream.

Typical feed streams used in step a) of the process according to the invention, such as natural gas or refinery gas streams and synthesis gas, may comprise valuable hydrocarbons, such as olefins, as well as alkanes, such as methane, ethane, propane, butane, pentane, hexane, heptane and octane.

It will be appreciated that the molar amount of hydrocarbons in the enriched absorbent stream produced in step a) of the process of the present invention is kept low relative to the molar amount of hydrocarbons in the feed stream.

In an embodiment of the method according to the invention, the feed stream comprises carbon dioxide and the CO in the feed stream of step a) is₂The amount is at least 5% volume,hereinafter vol%]Preferably at least 10 vol.%, preferably at least 15 vol.%, preferably at least 20 vol.%, preferably at least 25 vol.%, preferably at least 30 vol.%, preferably at least 35 vol.%, preferably at least 40 vol.%, preferably at least 45 vol.%, preferably at least 50 vol.%, preferably at least 55 vol.%, preferably at least 60 vol.%, preferably at least 65 vol.%.

In an embodiment of the process according to the invention, the feed stream comprises hydrogen sulphide, the amount of hydrogen sulphide in the feed stream of step a) being: at least 1 vol.%, preferably at least 5 vol.%, preferably at least 8 vol.%, preferably at least 10 vol.%, preferably at least 12 vol.%, preferably at least 15 vol.%, preferably at least 18 vol.%.

In an embodiment of the process according to the invention, the feed stream comprises carbonyl sulphide and the amount of carbonyl sulphide in the feed stream entering step a) is: at least 0.1ppmv, preferably at least 0.5ppmv, preferably at least 1ppmv, preferably at least 5ppmv, preferably at least 10ppmv, preferably at least 15ppmv, preferably at least 20ppmv, preferably at least 30ppmv, preferably at least 40ppmv, preferably at least 50ppmv, preferably at least 100ppmv, preferably at least 150ppmv, preferably at least 200ppmv, preferably at least 300ppmv, preferably at least 400ppmv, preferably at least 500ppmv, preferably at least 1000ppmv, preferably at least 1500ppmv, preferably at least 2000ppmv, preferably at least 3000ppmv, preferably at least 4000ppmv, preferably at least 5000ppmv, preferably at least 6000ppmv, preferably at least 7000ppmv, preferably at least 8000ppmv, preferably at least 9000ppmv, preferably at least 10000 ppmv. The applicant has found that the absorbent stream according to the invention is particularly effective for removing mercaptans.

In a more preferred embodiment of the process according to the invention, the feed stream comprises mercaptans and the amount of mercaptans in the feed stream to step a) is: at least 0.1 parts per million volume ratio [ parts per milliton by volume, hereinafter ppmv ], preferably at least 0.5ppmv, preferably at least 1ppmv, preferably at least 5ppmv, preferably at least 10ppmv, preferably at least 15ppmv, preferably at least 20ppmv, preferably at least 30ppmv, preferably at least 40ppmv, preferably at least 50ppmv, preferably at least 100ppmv, preferably at least 150ppmv, preferably at least 200ppmv, preferably at least 300ppmv, preferably at least 400ppmv, preferably at least 500ppmv, preferably at least 600ppmv, preferably at least 700ppmv, preferably at least 800ppmv, preferably at least 900ppmv, preferably at least 1000ppmv, preferably at least 1100ppmv, preferably at least 1200ppmv, preferably at least 1300ppmv, preferably at least 1400ppmv, preferably at least 1500ppmv, preferably at least 2000ppmv, preferably at least 3000ppmv, preferably at least 4000ppmv, preferably at least 10000 ppmv. The applicant has found that the absorbent stream according to the invention is particularly effective for removing mercaptans.

It is also to be understood that the term "moving flowing feed stream" may refer to a liquid or gaseous moving flowing feed stream.

In an embodiment of the method according to the invention, the feed stream is a moving flowing feed stream of gas, which is contacted with a liquid static absorbent stream. This example is clearly illustrated in the following example, which is performed on a laboratory scale.

In another embodiment of the process according to the invention, the feed stream is a moving flowing feed stream of liquid or gas, which is contacted with a moving flowing absorbent stream of liquid. This embodiment is clearly illustrated in the absorber column 1 of fig. 1, which absorber column 1 inherently comprises two streams split between the top and the bottom.

In an embodiment of the process according to the invention, step a) is carried out at a pressure of: at least 1 bar gauge (barggauge), preferably at least 5 bar gauge, preferably at least 10 bar gauge, more preferably at least 15 bar gauge, even more preferably at least 20 bar gauge, and yet more preferably at least 25 bar gauge. The applicant has found that the absorbent stream according to the invention is particularly effective and efficient at these higher pressures as exemplified.

In an embodiment of the process according to the invention, step a) is carried out at a pressure of: at most 150 bar gauge, preferably at most 120 bar gauge, more preferably at most 100 bar gauge, even more preferably at most 90 bar gauge. The applicant has found that a higher pressure does not bring much further improvement to the performance of step a). Applicants have found that if the feed stream needs to be pressurized in preparation for step a), the energy of further compression (to achieve a pressure above the levels listed) is generally not reasonable in view of the additional benefits obtainable.

In an embodiment of the method according to the invention, step a) is carried out at a temperature of: at least 10 ℃, preferably at least 20 ℃, more preferably at least 30 ℃, even more preferably at least 40 ℃.

In an embodiment of the method according to the invention, step a) is carried out at a temperature of: at most 90 ℃, preferably at most 80 ℃, more preferably at most 70 ℃, even more preferably at most 65 ℃.

In an embodiment, the process according to the invention further comprises step c), wherein at least part of the regenerated absorbent stream from step b) may be recycled to step a) as at least part of the absorbent stream.

In an embodiment of the method according to the invention, step b) comprises the steps of: in the stripping column, at least a portion of the impurity-enriched absorbent stream obtained from step a) is stripped, by convection with a gas stream containing water vapor, to form a bottom liquid stream, which is the first regenerated absorbent stream for recycling in step c). The applicant has found that stripping as specified above is a very efficient method for breaking the bond between the impurities and the absorbent stream and for separating the impurities from the absorbent stream.

In an embodiment of the method according to the invention, step b) comprises the steps of: flashing at least a portion of the impurity-enriched absorbent stream obtained in step a) to a lower pressure to release an impurity-containing gas stream from the liquid stream, which is the second regenerated absorbent stream for recycling in step c). Applicants have found that flashing can be an even more efficient process than stripping for disrupting the bond between the impurities and the absorbent stream and for separating the impurities from the absorbent stream. Applicants prefer to combine the flashing step with a downstream regeneration step, preferably a steam stripping step.

In an embodiment of the process according to the invention, the second regenerated absorbent stream is recycled to step a). Applicants found that the flashing step may produce a second regenerated absorbent stream, which is suitable for recycling to step a) in step c). This brings about the advantage that: this part of the absorbent stream does not necessarily need to be treated by a more thorough regeneration step, such as by stripping, before it is suitable to participate in step a).

In an embodiment of the process according to the invention, in step b) a first regenerated absorbent stream and a second regenerated absorbent stream are formed for recycling in step c), wherein the second regenerated absorbent stream contains more impurities than the first regenerated absorbent stream, preferably step a) is carried out in an absorption column and the first regenerated absorbent stream is recycled to a top liquid feed tray in the absorption column and the second regenerated absorbent stream is recycled to a middle feed tray in the absorption column, which is located below the top liquid feed tray. The applicant has found that this embodiment makes full use of the presence of the flash step without increasing the risk of breakthrough of impurities in step a), since the feed stream in contact with the second regenerated absorbent stream still has to pass through the region in which it is in contact with the first regenerated absorbent stream.

It is also understood that all definitions and preferences (as described above) of the mixture (M) used in step a) of the process according to the invention apply equally to this and all other examples described below.

Another aspect of the present invention is the mixture (M) as detailed above.

Another aspect of the invention is a composition comprising the mixture (M) as detailed above.

Another aspect of the invention is an absorbent stream comprising the mixture (M) as detailed above.

Another aspect of the invention provides the use of an absorbent stream comprising: mixture (M) as detailed above, or at least 15% by weight of at least one compound (a) as detailed above.

In another aspect, the present invention provides an impurity enriched absorbentA stream comprising at least one absorbed impurity selected from the group consisting of hydrogen sulfide (H)₂S), carbon dioxide (CO)₂) Carbon Oxysulfide (COS), carbon disulfide (CS)₂) A disulfide or thiol; the absorbent stream comprises: mixture (M) as detailed above, or at least 15% by weight of at least one compound (a) as detailed above.

FIG. 1 is a schematic diagram of an apparatus for removing impurities from a gas feed stream according to the process of the present invention. As shown in fig. 1, a gas feed is introduced into the absorption column 1 through a feed inlet 4 for impurity-containing gas. In the packed section 2, a gas feed stream placed in the absorption column 1 is brought into counter-current contact with an absorbent stream fed from a nozzle 7, impurities are absorbed by the absorbent stream and removed from the gas, and the gas depleted in impurities is discharged through an impurity-depleted gas discharge port 5. The absorbent stream fed to the absorption column 1 absorbs impurities and is led to the heat exchanger 14 and the heater 8, heated and led to the regeneration column 15. In the regeneration column 15, the absorbent stream flows through the nozzle 16 and the packed section 17 to the lower part of the column. During this time, impurities are removed to regenerate the absorbent stream. A portion of the absorbent stream at the bottom of the regenerator column is sent through reboiler 27 to produce a vapor stream for stripping the absorbent stream falling from the column. The regenerated absorbent stream is introduced into the heat exchanger 14 and the absorbent stream cooler 26 by the pump 9 and fed back into the absorption column 1 through the absorbent stream feed inlet 6.

On the other hand, in the upper part of the regeneration tower 15, the impurities removed from the absorbent flow are contacted with the reflux water entering from the nozzle 18 and cooled by the regeneration tower reflux condenser 23, and in the reflux tank 21, the gas impurities are separated from the reflux water (formed by condensing the water vapor accompanied with the impurities) and may be introduced to the impurity recovery step through the recovered impurity line 22. The reflux water enters the regeneration tower 15 through a reflux water pump 20.

Examples of the invention

The invention will now be described in more detail with reference to the following examples, which are intended to be illustrative only and are not intended to limit the scope of the invention.

Overall procedure for determining absorbency

All experiments were carried out using a 30g absorbent stream. The laboratory scale absorption experiments were performed by: contacting a feed stream gas mixture comprising 1000ppmv (parts per million by volume) n-butane and 1000ppmv methyl mercaptan (CH) with various absorbent streams at a temperature of 40 ℃ and a pressure of 2 bar₃SH) -under nitrogen. The absorption unit of the experiment comprised a double-walled tubular absorber of 7mm diameter, equipped with a thermocouple and heated by a water bath. A back pressure regulator installed downstream of the tubular absorber was used to maintain the pressure within the absorber at a constant pressure. Gas flow rate of 5.1L.h^-1The resulting impurity-depleted product stream Gas is depleted in n-butane and methyl mercaptan as the feed stream Gas mixture passes through the absorbent stream in an upward direction until the impurity-enriched absorbent stream becomes saturated.A Gas Chromatography (GC) is used with an Agilent 7890B Gas Chromatograph equipped with split injectors (split injectors) and a flame ionization detector (290 ℃), the composition of the outlet Gas is analyzed at regular intervals.A capillary Rtx-Volatile Amine Column (Rtx-Volatile Amine Column) with a size of 60 meters × 0.32 millimeter ID is used (Rtx-Volatile Amine Column). the GC temperature is set at 40 ℃, Gas samples are injected at a split ratio of 100: 1.OpenLAB Chromatography Data system (OpenLAB Chromatography Data Systems) software is used for Data collection and Data processing.Once at room temperature, the contents are opened, transferred into a glass oven, and sampled for composition analysis to determine the composition of the OpenLAB Chromatography Data system.A continuous cycle of the absorber is evaluated for at least two Lv. 80 ℃ regeneration cycles of the absorber without heating.

In order to compare the performance of the different absorbent streams, the concentration of methyl mercaptan and n-butane in the exit gas was followed in time. The concentration of methyl mercaptan and/or n-butane in the outlet gas is zero as long as the absorbent stream is unsaturated. Once the absorbent stream is nearly saturated, the exit concentration of methyl and/or n-butane (in ppmv) begins to increase (i.e., breakthrough). This breakthrough occurs at different times for different absorbent flows. The solvent loading was estimated by integrating the area above these respective "breakthrough" curves (i.e., ppmv concentration of methyl mercaptan or n-butane in the outlet gas as a function of time (in minutes)) and by subtracting the amount of gas used to fill the absorber headspace. The amount of absorbed methyl mercaptan and n-butane was calculated by writing the following formula:

whereinIs the flow rate of the gas phase (NL.h)^-1) And m is the total mass (g) of the absorbent stream.

A list of materials used according to the invention can be found in table 1.

Table 1: product listing and description

Compound (A) according to the invention	Description of the invention
		DMAP-2-PYRROLIDONE	Dimethylaminopropyl-2-pyrrolidone
DMAE-2-PYRROLIDONE	Dimethylaminoethyl-2-pyrrolidone
		Compound (B) according to the invention	Description of the invention
N-tert-butyl-2-pyrrolidone	N-tert-butyl-2-pyrrolidone
		N-butyl-2-pyrrolidone	N-butyl-2-pyrrolidone
N-octyl-2-pyrrolidone	N-octyl-2-pyrrolidone
		Compound (B) according to the invention	Description of the invention
MDEA	Methyldiethanolamine
		Reference compound	Description of the invention
Sulfolane	Sulfolane
		2-pyrrolidone	2-pyrrolidone
N-methyl-2-pyrrolidone	N-methyl-2-pyrrolidone

Absorption Properties

Examples 1 to 2

The absorbent stream of examples 1-2 was a mixture (M) prepared by mixing 25 wt% of compound (B), 50 wt% of MDEA (i.e., compound (C)) and 25 wt% of water. The absorption performance data and the specific compounds (B) used are summarized in table 2 below.

Examples 3 to 4

The absorbent streams of examples 3-4 are compositions (C) prepared by mixing 25 wt% of compound (A), 50 wt% of MDEA (i.e., compound C), and 25 wt% of water. The absorption performance data and the specific compounds (a) used are summarized in table 2 below.

Comparative examples 5 to 7

The absorbent streams of comparative examples 5-7 were prepared following the same procedure as in examples 1-2, except that the reference compound used was not compound (B) according to formula (II). Specifically, sulfolane was used in comparative example 5, 2-pyrrolidone was used in comparative example 6, and N-methyl-2-pyrrolidone was used in comparative example 7. The absorption performance data of comparative example 5 is considered a reference since the sulfolane containing absorbent stream is similar to the well known commercially available absorbent stream

A solvent. The absorption performance data are summarized in table 2 below.

TABLE 2

For comparison purposes, it should be noted that the reference absorbent solution of comparative example 5, containing sulfolane, can capture 3.64 to 3.67mmol of CH per kilogram of solvent₃SH and 0.26-0.35mmol C₄H₁₀(Table 2). In the case of N-butyl-2-pyrrolidone (example 1), it was observed that: 4.11-5.64mmol of CH per kg of solvent₃SH loading, and 0.33-0.37mmol of C₄H₁₀The amount of the supported. Under the same conditions, the results also show that the CH of N-octyl-2-pyrrolidone (example 2), DMAP-2-pyrrolidone (example 3) and DMAE-2-pyrrolidone (example 4) is compared to the reference absorbent solution of comparative example 5 containing sulfolane₃The SH-absorbing ability is equivalent or superior. We conclude that these specific substitutions on the amide nitrogen of the pyrrolidone ring have a positive effect on the interaction of the absorbent stream with mercaptans while maintaining a low co-absorption of hydrocarbons (e.g. n-butane). Table 2 further shows the reactionsCH of comparative absorbent solutions in comparative examples 5 to 7₃SH absorption number in comparison with CH of the absorbent stream according to the invention (examples 1 to 4)₃The SH absorption values are comparable or better.

Example 8

The absorbent stream of example 8 is a mixture (M) which is prepared by mixing 30% by weight of N-butyl-2-pyrrolidone, i.e.compound (B), with 50% by weight of MDEA, i.e.compound (C), and 25% by weight of water. The absorption performance data are summarized in table 3 below.

Comparative example 9

The absorbent stream of comparative example 9 was prepared following the same procedure as example 8, except that 30 wt% of sulfolane, which is not compound (B) according to formula (II), was used. The absorption performance data are summarized in table 3 below.

Table 3 shows typical absorption data (n) for three consecutive absorption-regeneration cycles for the reference absorbent stream of comparative example 9 and the absorbent stream according to the invention (example 8)_{Absorption of}) The reference absorbent stream of comparative example 9 comprises 30 wt% sulfolane and the absorbent stream according to the invention (example 8) comprises 30 wt% n-butyl-2-pyrrolidone (i.e. compound B).

TABLE 3

Example 10

The absorbent stream of example 10 was a mixture (M) prepared by mixing 15 wt% of N-butyl-2-pyrrolidone (i.e., compound (B)) with 50 wt% of MDEA (i.e., compound (C)) and 25 wt% of water. The absorption performance data are summarized in table 4 below.

Comparative example 11

The absorbent stream of comparative example 11 was prepared following the same procedure as example 10, except that 15 wt% of sulfolane, which is not compound (B) according to formula (II), was used. The absorption performance data are summarized in table 4 below.

Table 4 shows three successive aspirations for the reference absorbent flow of comparative example 11 and the absorbent flow according to the invention (example 10)Typical absorption data (n) of a regeneration-receiving cycle_{Absorption of}) The reference absorbent stream of comparative example 11 contains 15 wt% sulfolane and the absorbent stream according to the invention (example 10) contains 15 wt% n-butyl-2-pyrrolidone (i.e. compound B).

TABLE 4

The effect of different concentrations of compound B was investigated by varying the proportions of the different absorbent stream components (examples 8 and 10) and by comparing the results with reference absorbent streams comprising sulfolane (comparative examples 9 and 11). The absorbent solution according to the invention (comprising N-butyl-2-pyrrolidone) shows an consistently higher CH than the reference absorbent solution of the comparative example₃The solubility of SH, while the co-absorption of n-butane remains low.