Catalysis of the reaction between hydrogen sulfide scavengers and hydrogen sulfide using tertiary amines

Abstract

While some triazines have low reactivity, a method and composition is described for improving their reactivity. The H.sub.2S scavenging composition and method utilizes a tertiary amine to catalyze the scavengers with slower kinetics to achieve improved results over traditional systems with the scavenger alone. A hydrogen sulfide scavenging composition comprises: a tertiary amine as a catalyst in at least one of (i) a triazine scavenger selected from the group consisting of: methyl amine, C2-C5 alkyl amine, dimethylaminopropylamine, isopropanolamine, aniline, cyclohexylamine, isobutanolamine and methoxypropylamine triazines/bisoxazolidines; or (ii) an aldehyde-based scavenger such as glyoxal.

Claims

1. A hydrogen sulfide scavenging composition comprising: a scavenger selected from the group consisting of methyl amine, C2-C5 alkyl amine, dimethylaminopropylamine, isopropanolamine, aniline, cyclohexylamine, isobutanolamine and methoxypropylamine triazines/bisoxazolidines, and; a tertiary amine.

2. The composition according to claim 1 wherein the scavenger chemistry is methyl amine triazine or dimethylaminopropylamine triazine or bisoxazolidines.

3. The composition of claim 1 wherein the tertiary amine is selected from the group consisting of: triethylamine (TEA), tripropylamine (TPA), tributylamine (TBA) and dimethylaminopropylamine (DMAPA).

4. The composition of claim 1 wherein the tertiary amine has a concentration of to 10% by volume in the scavenger.

5. A method for scavenging hydrogen sulfide from a sour hydrocarbon fluid comprising: contacting the sour hydrocarbon fluid with a hydrogen sulfide scavenging composition comprising: a scavenger selected from the group consisting of: methyl amine, C2-C5 alkyl amine, dimethylaminopropylamine, isopropanolamine, aniline, cyclohexylamine, isobutanolamine and methoxypropylamine triazines/bisoxazolidines, and; a tertiary amine.

6. The method according to claim 5 wherein the scavenger chemistry is methyl amine triazine or dimethylaminopropylamine triazine or bisoxazolidines thereof.

7. The method according to claim 5 wherein the tertiary amine is selected from the group consisting of: triethylamine (TEA), tripropylamine (TPA), tributylamine (TBA) and dimethylaminopropylamine (DMAPA).

8. The method according to claim 5 wherein the tertiary amine has a concentration of 0.1 to 10% by volume in the scavenger.

9. A hydrogen sulfide scavenging composition comprising: an aldehyde-based H.sub.2S scavenger; and a tertiary amine.

10. The composition according to claim 9 wherein the aldehyde-based H.sub.2S scavenger is glyoxal.

11. The composition of claim 9 wherein the tertiary amine is selected from the group consisting of: triethylamine (TEA), tripropylamine (TPA), tributylamine (TBA) and dimethylaminopropylamine (DMAPA).

12. The composition of claim 9 wherein the tertiary amine has a concentration of to 10% by volume in the aldehyde-based H.sub.2S scavenger.

13. A method for scavenging hydrogen sulfide from a sour hydrocarbon fluid comprising: contacting the sour hydrocarbon fluid with a hydrogen sulfide scavenging composition comprising: an aldehyde-based H.sub.2S scavenger, and; a tertiary amine.

14. The method according to claim 13 wherein the aldehyde-based H.sub.2S scavenger is glyoxal.

15. The method according to claim 13 wherein the tertiary amine is selected from the group consisting of: triethylamine (TEA), tripropylamine (TPA), tributylamine (TBA) and dimethylaminopropylamine (DMAPA).

16. The method according to claim 13 wherein the tertiary amine has a concentration of 0.1 to 10% in the scavenger.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0013] FIG. 1 is a schematic of the H2S breakthrough test setup.

[0014] FIG. 2 shows slippage data for 35% MMA triazine scavenger solutions alone and catalyzed with tertiary amines according to Example I.

[0015] FIG. 3 shows foaming tendency of the 35% MMA triazine solutions during the course of the test.

[0016] FIG. 4 shows slippage data from Example II for a 40% glyoxal scavenger solution alone and catalyzed with a tertiary amine.

[0017] FIG. 5 shows the result of hydrogen sulfide pressure drop as a result of reactivity with a 40% glyoxal scavenger solution alone and catalyzed with a tertiary amine, as in Example III.

DETAILED DESCRIPTION OF THE INVENTION

[0018] In one embodiment, the present invention provides a new hydrogen sulfide scavenger composition comprising a scavenger chemistry catalyzed by a tertiary amine. The invention is particularly useful for improving the reactivity of less reactive scavengers.

[0019] In one embodiment, the H.sub.2S scavenger is a substituted triazine scavenger including methyl amine (MMA) triazine, other alkyl amine (C2-C5) triazines, dimethylaminopropylamine (DMAPA) triazine, isopropanolamine triazine, aniline triazine, cyclohexylamine triazine, isobutanolamine triazine or methoxypropylamine (MOPA) triazine. The foregoing triazines have been considered to have slow reactivity, in particular a reactivity much less than that of monoethanolamine (MEA) triazine, and a modification that will increase their reactivity is of interest.

[0020] Triazines are the reaction products of three moles of amine with three moles of formaldehyde. Thus, it is to be understood that a mixture of formaldehyde and the above-noted amines is captured by the terms triazine and triazine-based scavenger and the like.

[0021] For certain hydroxyalkyl amines, reaction of three moles of formaldehyde with two moles of a hydroxyalkyl amine followed by dehydration can result in a biscyclized bridged moiety. As an example, three moles of formaldehyde reacted with two moles of isopropanolamine produces bisoxozolidine (oxazolidine, 3,3-methylenebis[5-methyl-]). Note that in aqueous solution, the bisoxozolidine behaves as if it were isopropanolamine triazine with an excess of formaldehyde. Thus, herein it is to be understood that triazine, triazine-based scavenger and the like terms, include bisoxozolidines.

[0022] In another embodiment, the H.sub.2S scavengers are aldehyde-based, including, but not limited to glyoxal, acrolein and others.

[0023] The addition of a tertiary amine has been found to improve the reaction between the scavenger and H.sub.2S. While it is not necessary to identify the mode of the effect, it is believed that the added tertiary amine acts as a catalyst for the reaction of the scavenger chemistry and H.sub.2S. In particular, with reference to triazines, unlike primary amines which would form triazines (when reacted with formaldehyde), tertiary amines such as triethylamine, tripropylamine and tributylamine have been found not to react with formaldehyde. Therefore, although it is not intended that the invention be limited by the theory, it is believed that the improved performance with the addition of amine to the scavenger is catalytic in nature.

[0024] The tertiary amines are useful in catalytic amounts, such as up to 10% by volume in the scavenger. For example, concentrations of 0.05 to 8.0% or 0.1 to 5.5% by volume are useful to catalyze the reaction between a triazine-based or aldehyde-based scavenger and H.sub.2S.

[0025] The tertiary amines of greatest interest are triethylamine (TEA), tripropylamine (TPA), tributylamine (TBA) and dimethylaminopropylamine (DMAPA). It would be appreciated that DMAPA may not be useful to catalyze the reaction of a DMAPA triazine with H.sub.2S.

[0026] While the H.sub.2S scavengers and tertiary amines are the reactants of interest in this invention, it will be appreciated that a hydrogen sulfide scavenger composition may contain other chemicals such as methanol, glycol, etc.

[0027] The following examples show that the reaction of MMA triazine or glyoxal with H.sub.2S can be catalyzed using triethylamine. The beneficial effect of tripropylamine and dimethylaminopropylamine (DMAPA) on the reaction of MMA triazine with H.sub.2S is also exemplified. The invention is not to be limited by the examples, since it is submitted that these and other tertiary amines can catalyze the reaction of triazine/bisoxazolidine scavengers or aldehyde-based scavengers with H.sub.2S.

EXAMPLES

[0028] Example ITo verify the potential positive effects of tertiary amines on the performance of triazine based H.sub.2S scavengers, H.sub.2S breakthrough tests were performed using 35% MMA triazine solutions, as the benchmark for the study.

[0029] H.sub.2S breakthrough tests are used to evaluate performance of scavenger solutions for application in bubble/contact towers. A schematic diagram of the test setup is shown in FIG. 1.

[0030] In each breakthrough test, a 50 mL sample of the H.sub.2S scavenger of interest was put in the contactor of the breakthrough apparatus. The sample was purged with a gas mixture containing 10% H.sub.2S (in nitrogen) at a flow rate of 211 mL/min. The scavenged gas, was then passed through a Drager tube. H.sub.2S slippage through the scavenger is recorded as a function of time. In this test, the breakthrough time is reported as the time required until the 0.2% (2000 ppm) reading level is reached on the Drager tube. Once breakthrough is observed, the test continues until the 7% reading on the Drager tube is reached. The tests were performed at 30 C.

[0031] Table 1 shows the breakthrough time for the 35% MMA triazine, 35% MMA triazine+1 TPA, 35% MMA triazine+1% DMAPA, and 35% MMA triazine+1% TEA samples. All testing was at 30 C.

TABLE-US-00001 TABLE 1 Breakthrough test results for 35% MMA Triazine Scavenger Temperature Breakthrough Appearance Product ( C.) Time (min) Post-Test 35% MMA Triazine 30 9.3 Clear colorless solution 35% MMA Triazine + 30 16.1 Clear colorless 1% TPA solution 35% MMA Triazine + 30 33.0 Clear colorless 1% DMAPA solution 35% MMA Triazine + 30 57.0 Clear colorless 1% TEA solution

[0032] The breakthrough time for the 35% MMA triazine, 35% MMA triazine+1% TPA, 35% MMA triazine+1% DMAPA, and 35% MMA triazine+1% TEA, under the test conditions, were measured as 9.3, 16.1, 33.0, and 57.0 minutes, respectively.

[0033] For the test a Drager tube with the range of 0.2-7% was used. After the initial breakthrough, observing the progression of the color change can give a qualitative indication towards the concentration of H.sub.2S slipping past the contactor. The slippage data are presented in the following table (Table 2) and in FIG. 2.

TABLE-US-00002 TABLE 2 Slippage data for 35% MMA Triazine 35% MMA 35% MMA 35% MMA Cumulative 35% MMA Triazine + Triazine + Triazine + Reading Triazine 1% TPA 1% DMAPA 1% TEA (%) (min) (min) (min) (min) 0.2 9.3 16.1 33.0 57.0 0.5 14.1 19.8 45.0 62.0 1.0 20.8 26.4 53.0 67.0 1.5 26.3 33.0 58.0 71.0 2.0 31.8 37.8 62.8 74.0 2.5 36.3 42.4 67.2 77.0 3.0 40.3 46.1 71.2 80.0 3.5 43.6 49.8 74.5 83.0 4.0 46.9 52.8 78.0 86.0 4.5 49.9 56.0 81.9 89.1 5.0 52.4 59.2 85.0 91.3 5.5 55.3 62.4 88.0 93.5 6.0 57.9 65.8 90.7 96.3 6.5 60.3 68.8 93.2 98.6 7.0 62.6 71.7 95.6 100.9

[0034] As shown in the diagram, the presence of the amines has improved performance of the 35% MMA triazine, under the test conditions. TEA offered the best improvement.

[0035] All scavenger solutions were clear post-test, with no noticeable turbidity.

[0036] FIG. 3 shows foaming tendency of the scavenger solutions during the course of the test. As shown, the presence of TPA, DMAPA, and TEA did not cause any significant change in foaming tendency of the 35% MMA triazine, under the test conditions.

[0037] Based on the test results, addition of low levels of TPA, DMAPA, and TEA each provided improved performance of MMA triazine scavenger. TPA showed the least improvement and TEA the most significant improvement. The amines did not cause any significant alterations in foaming tendency of the scavenger solutions, under the test conditions. The partially spent 35% MMA triazine solutions were clear post-test, with no noticeable turbidity.

Example II

[0038] Breakthrough testing, as described above, was repeated with 40% glyoxal solution and 40% glyoxal solution with 5% TEA.

[0039] Results are shown in FIG. 4. As noted above, the longer the time before H.sub.2S is detected, the better the scavenger performance.

[0040] Non-catalyzed glyoxal had a breakthrough time of 30 seconds. 40% glyoxal catalyzed with 5% TEA had a breakthrough time of 14 minutes.

Example III

[0041] 15.2 mL of either 40% glyoxal solution or 40% glyoxal solution catalyzed with 1% TEA was placed in an autoclave. The autoclave was pressurized to 160 psi with H.sub.2S.

[0042] The autoclave gauge pressure is recorded as a function of time. A pressure drop is indicative of consumption of H.sub.2S.

[0043] A fast pressure drop is indicative of improved scavenger kinetics.

[0044] Results are shown in FIG. 5.

[0045] The autoclave pressure with 40% glyoxal solution dropped from 160 psi to 100 psi in 100 minutes.

[0046] The autoclave pressure with 40% glyoxal solution catalyzed with 1% TEA dropped from 160 psi to 100 psi in 30 minutes.

[0047] Based on the test results, addition of low levels of tertiary amines will improve the performance of glyoxal and potentially other aldehyde-based scavengers.

[0048] The previous description of the disclosed embodiments is provided to enable any person skilled in the art to make or use the present invention. Various modifications to those embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without departing from the spirit or scope of the invention. Thus, the present invention is not intended to be limited to the embodiments shown or presented in the examples herein, but is to be accorded the full scope consistent with the claims, wherein reference to an element in the singular, such as by use of the article a or an is not intended to mean one and only one unless specifically so stated, but rather one or more. All structural and functional equivalents to the elements of the various embodiments described throughout the disclosure that are known or later come to be known to those of ordinary skill in the art are intended to be encompassed by the elements of the claims. Moreover, nothing disclosed herein is intended to be dedicated to the public regardless of whether such disclosure is explicitly recited in the claims. No claim element is to be construed under the provisions of 35 USC 112, sixth paragraph, unless the element is expressly recited using the phrase means for or step for.