Patent Application
20190184383
This application is in the field of technologies for desulfurization and demercaptanization of raw gaseous hydrocarbons (including natural gas, tail gas, technological gas, etc., including gaseous media). It can be used for simultaneous dehydration and desulfurization/demercaptanization of any kind of raw gaseous hydrocarbons.
A prior art (U.S. Pat. No. 4,622,212, issued Nov. 11, 1986) describes a process of liquid-state oxidation of hydrogen sulfide to sulfur by means of chelating complexes of iron (Lo-Cat process). In the Lo-Cat process, a catalytic reactor for conversion of hydrogen sulfide into sulfur is used, and a device to regenerate the catalyst solution.
The said process features insufficient degree of desulfurization and incapability of demercaptanization and dehydration that must be admitted as its drawbacks.
A prior art (U.S. Pat. No. 8,735,316, issued. May 27, 2014) describes a process of catalytic demercaptanization by converting mercaptans to disulfides. As a catalyst, the complex CuCl with monoethanol amine (MEA), acetonitrile, or with a monobasic alcohol is used. The process flows in presence of air oxygen, at a temperature of 22-140° C. The residual amount of mercaptan sulfur can be reduced to 20 ppm.
The said process is capable of purifying only liquid media, and no data is provided concerning its capability of hydrogen sulfide removal and/or water removal, that must be admitted as the drawbacks.
A prior art (RU, patent No. 2385180 issued. Mar. 27, 2010) describes a Claus-process of conversion of hydrogen sulfide to sulfur.
The said art features primary amine treatment of the gas to be purified, multiple stages of the process and insufficient conversion of hydrogen sulfide to sulfur, necessity of tail gas treatment, sophisticated technological equipment, and incapability of demercaptanization and dehydration, all these items must be admitted as the drawbacks.
A prior art (U.S. Pat. No. 5,286,697, issued Feb. 15, 1994) also describes an improved Claus process.
The said art is also incapable of demercaptanization and dehydration, and it is less efficient in hydrogen sulfide conversion.
A prior art (RU, patent No. 2405738, issued Apr. 27, 2010) describes a means of sulfur recovery from industrial gases by means of a catalyst that contains on dehydroxylated silica gel (97.65% by mass) impregnated with ferric phosphate (III) (2.35%), that provides sulfur formation from hydrogen sulfide that is present in gaseous hydrocarbons.
The said art features insufficient conversion of hydrogen sulfide, and catalyst production complexity, incapability of gas dehydration, that must be admitted as drawbacks.
A prior art (RU, patent No. 2398735, issued Sep. 10, 2010) describes a means of gas desulfurization by oxidating hydrogen sulfide to elemental sulfur in liquid state in presence of a catalyst, which contains a compound of a transition metal and an organic complexing agent. To oxidate hydrogen sulfide, it is proposed to use air oxygen as oxidizer; as a compound of transition metal, cupric halogenide is used, where the amount of copper in the solution is 0.015 to 0.1% by weight, and where as an organic complexing agents, one of the following is used: dimethylformamide, pyrrolidone, methylpyrrolidone, pyridine, or quinolone; the process flows in a solvent that is taken as one of the following: monobasic alcohol, polybasic alcohol, water, or their mixtures, kerosene, isooctane, gas condensate at temperature of 20-40° C.
The drawbacks of the said process are its capability of gas desulfurization only, incapability of gas dehydration.
The closest technical solution to one described in the current claim can be considered the prior art (RU,2127146,
Mar. 10, 1999) that describes a process of gaseous hydrocarbon purification to H2S level below 4 ppm vol. and dehydration with dew point temperature in between 0° C. and −18° C. The said closest technical solution provides desulfurization and dehydration of the gas by applying a solution of “amine-glycol”. The said process does not provide conversion of hydrogen sulfide into sulfur. Hydrogen sulfide extracted from the gas undergoes afterburning with generation of sulfur dioxide.
The drawbacks of the said process are related to hydrogen sulfide conversion to sulfur dioxide, that requires disposal, and incapability of demercaptanization.
Current invention claim is free from the drawbacks of the prior art described above, in that it is capable of simultaneous gas dehydration and demercaptanization, where mercaptan sulfur recovery rate is over 99%, with no athmospheric emissions or any waste that requires disposal.
The technical problem solved by current invention is in developing a technical solution that provides simultaneous dehydration, desulfurization and demercaptanization while SH recovery rate is above 99.999%.
The technical result achieved in realization of proposed solution is a single-stage desulfurization and demercaptanization of gaseous hydrocarbons simultaneously with their dehydration while providing residual amount of —SH down to 0.001 ppmand producing no waste.
To achieve the said technical result, it is proposed to use the developed device for dehydration, desulfurization and demercaptanization of gaseous hydrocarbons. The proposed device for dehydration, desulfurization and demercaptanization of gaseous hydrocarbons is based on a device for absorptive gas dehydration where working temperature and pressure of the gas, and the composition of the absorbent are determined by requirements to gas dehydration. The proposed device features a reactor for desulfurization/demercaptanization/dehydration loaded with solution of a catalyst for conversion of hydrogen sulfide and mercaptans into sulfur and disulfides, respectively, dissolved in an absorbent. The proposed devices also features a unit for absorbent regeneration and sulfur separation.
While the gas is passed through absorbent solution of the catalyst the hydrogen sulfide and the mercaptans convert to sulfur and disulfides, respectively, in accordance with reaction formula:
H2S+2RSH+O2═S+RSSR+2H2O (1)
The disulfides formed in reaction (1) remain in the reactor, and they do not affect the main process in any way. The water is absorbed by the absorbent solution, and it is withdrawn from the reactor together with fine sulfur dispersion. The purified and dehydrated gas is given out to the end user from the reactor outlet. The absorbent solution together with fine sulfur dispersion is passed over for regeneration and sulfur separation.
The device provides for a unit for sulfur pulp withdrawal from the reactor to the unit for absorbent regeneration and sulfur separation. In addition, the said device includes at least a means of supplying the gaseous hydrocarbons to be purified and the oxygen-containing gas into the reactor, a means of withdrawing the purified gas from the reactor, and the unit for absorbent regeneration and sulfur separation includes a means of absorbent regeneration and a means of sulfur removal from the unit, where the reactor design and catalyst composition provide conversion of at least 99.99% of hydrogen sulfide and mercaptans into sulfur and disulfides, respectively, with simultaneous water absorption by the absorbent in order to provide the required level of gas dehydration, and where the unit for absorbent regeneration provides for removing water from it with later absorbent recycling into desulfurization/demercaptanization/dehydration reactor.
In the preferred embodiment the means of supplying the gaseous hydrocarbons to be purified and the oxygen-containing gas additionally include a means of mixing the gaseous hydrocarbons to be purified with the oxygen-containing gas and homogenization of the resulting gas mixture, and the desulfurization/demercaptanization/dehydration reactor includes a means for distributing the supplied gas mixture in the reactor volume.
In some embodiments, the desulfurization/demercaptanization/dehydration reactor may additionally include filling plates.
In some embodiments, the device may additionally include a means of metered supply of the catalystinto desulfurization/demercaptanization/dehydration reactor, or into the unit for absorbent regeneration and sulfur separation, or into any other part of the device.
As a catalyst that provides the said technical result achievement, the device may use mixed-ligand complexes based on ferric and/or cupric halogenides. The any other catalyst composition may be used that provide achievement of the said technical result
The unit for absorbent regeneration and sulfur separation typically includes at least an inlet nozzle to inlet the catalyst solution for regeneration, an outlet nozzle to outlet the catalyst solution after regeneration, a nozzle to outlet the dissolved gas, a heater of the sulfur pulp in the absorbent, filling plates for absorbent dehydration, a water withdrawal nozzle to withdraw water that has been evaporated from the absorbent at its regeneration.
The means of sulfur withdrawal from the unit may be a pipe where liquid sulfur flows.
To achieve the said technical result it is proposed to use the developed process of dehydration/desulfurization/demercaptanization of gaseous hydrocarbons. In the said process, the gaseous hydrocarbons to be purified are mixed with an oxygen-containing gas, pressurized and passed through a reactor loaded with a catalyst for ozidating hydrogen sulfide and mercaptans dissolved in an absorbent that provides dehydration of the gas, where the catalyst is mixed-ligand complexes of transition metals, the conversion rate of hydrogen sulfide and mercaptans into sulfur and disulfides is at least 99.99%, and where the gas pressure determined by required moisture level in the purified medium.
Typically, the amount of oxygen is taken not less than 50% of total amount of hydrogen sulfide and mercaptan sulfur.
In some embodiments, the gas mixture supplied into the reactor is evenly distributed in the reactor volume.
Mostly due to catalyst loss, in the purification process, a metered supply of the catalyst is implemented.
Preferably, during the purification process, the fine sulfur dispersion is separated from the suspension by any known means, and the sulfur-free catalyst solution is recycled into the reactor.
Typically, as the absorbent for gas dehydration, glycols or glycol mixtures with organic compounds are used. At that, other absorbents may be used that provide achievement of the technical result said above.
Typically, in the said process a catalyst is used that is a 0.0001-100% solution in an organic solvent of mixed-ligand complexes based on ferric halogenide and/or cupric halogenide with addition of solvating agents.
As an agitator of oxygen-containing gas discharge, an air compressor can be used, as an agitator of catalyst solution supply from the tank—a metering pump, and as an agitator of catalyst solution recycling from sulfur-separating unit—a regular pump can be used.
Below, the essence and advantages of the developed technical solution are discussed in examples of practical implementation.
Synthesis of catalyst C1. Into a retort, at a room temperature, 50 ml of ethyl alcohol, 100 ml of octane, 0.2-10 g of CuCl2.2H2O and 0.5-50 g of benzylamine are put. The contents of the retort are mixed until cupric chloride dissolves completely.
Synthesis of catalyst C2. Into a retort, at a room temperature, 50 ml of ethyl alcohol, 100 ml of octane, 0.2-10 g of CuCl2.2H2O and 0.5-50 g of cyclohexamine are put. The contents of the retort are mixed until cupric chloride dissolves completely.
Synthesis of catalyst C3. Into a retort, at a room temperature, 50 ml of ethyl alcohol, 100 ml of octane, 0.2-10 g of CuCl2.2H2O and 0.5-50 g of pyridine are put. The contents of the retort are mixed until cupric chloride dissolves completely.
Synthesis of catalyst C4. Into a retort, at a room temperature, 50 ml of ethyl alcohol, 20 ml of water, 0.2-60 g of dimethylformamide (DMFA), and 0.2-10 g of CuCl2.2H2O are put. The contents of the flask are mixed by means of a magnetic mixer until cupric chloride dissolves completely.
Synthesis of catalyst C5. Into a retort, at a room temperature, 50 ml of alcohol as solvent, 0.2-60 g of mixture of amine (cyclohexamine, pyridine) with dimethylformamide (DMFA) as solvating agents, 0.2-10 g of CuCl2.2H2O are put. The contents of the flask are mixed until cupric chloride dissolves completely.
Similarly catalyst C5 was synthesized with other solvating agents and in other solvents.
Gas purification using catalysts C1-C5. The reactor is loaded with glycol and one of the catalysts C1-C5 synthesized as in examples 1-5, respectively. The gas supplied into the reactor contains 1%-2.2% vol. of hydrogen sulfide, 0.05% of mercaptan sulfur and 0.5025%-1.125% vol. of oxygen. The gas pressure is 2.5-60 kgf/cm2. The solution temperature is 25°-40° C. The output gas contains, according to potentiometric titration results, 0.001 ppm-70 ppm of hydrogen sulfide and mercaptan.
The rate of hydrogen sulfide removal is 99.6%-99.99999%, the rate of mercaptan removal is up to 99.998%. The rate of dehydration is determined by the gas pressure. The higher the gas pressure is, the lower amount of water remains in the output gas.
Experimental data on hydrogen sulfide, mercaptan and water contents after desulfurization/demercaptanization/dehydration of the gas using catalyst C1 is given in Table 1.
Experimental data on hydrogen sulfide, mercaptan and water contents after desulfurization/demercaptanization/dehydration of the gas using catalyst C2 at temperature 25°-40° C. and under different conditions is given in Table 2.
Experimental data given in Tables 1 and 2 show that the proposed device and process is capable of achieving the stated technical result even if the catalyst composition used is not optimal.
Experimental data on hydrogen sulfide, mercaptan and water contents after desulfurization/demercaptanization/dehydration of the gas using catalysts C1, C2, C3 at temperature 25°-40° C. and under different conditions is given in Table 3.
Experimental data on hydrogen sulfide, mercaptan and water contents after desulfurization/demercaptanization/dehydration of the gas using catalyst C4 at temperature 25°-40° C. and under different pressure is given in Table 4.
Experimental data on hydrogen sulfide, mercaptan and water (g/m3 and Tdew point, ° C., water dew point temperature at P=3.92 MPa) contents after desulfurization/demercaptanization/dehydration of the gas using catalyst C5 at temperature 25°-40° C. and under different pressure is given in Table 5.
Hydrogen sulfide and mercaptan conversion in Examples 6-27 is given in Table 6.
The examples provided show efficiency of the proposed device and process of hydrogen sulfide and mercaptans conversion. The amount of remaining water after dehydration therein is determined by process pressure and temperature, as is demonstrated in Tables 1-5. Under pressure 60 kgf/cm2 the water content in the gas is reduced to 0.074 g/m3, that corresponds to water dew point of −10° C.
Table 7 shows the results of gas purification by means of the proposed device and process with different concentration of catalyst C5. The conditions of the experiment are similar to those of experiments No. 6 -27, temperature is 25° C.
Table 8 shows results of purification and dehydration of gas having different hydrocarbon composition, with different contents of methane, C1, ethane, C2, and C3+ by proposed device and process, using catalyst K5. The conditions of experiments are similar to those of experiments No. 6 -27.
Table 9 shows results of purification by means of catalyst C5 with various solvating agents and in various solvents. The conditions of experiments are similar to those of experiments No. 6-27.
solvent:
The examples provided confirm achievement of the stated technical result, yet they do not show the limits of proposed technical solution.
It will be understood that the system and method may be embodied in other specific forms without departing from the spirit or central characteristics thereof. The present examples and embodiments, therefore, are to be considered in all respects as illustrative and not restrictive, and the system method is not to be limited to the details given herein.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2016116050 | Apr 2016 | RU | national |
The present application is a divisional application of U.S. patent application Ser. No. 16/150,718 filed on Oct. 3, 2018, which claims priority to U.S. patent application Ser. No. 15/539,882 filed Jun. 26, 2017 which is a National stage application from the PCT application PCT/RU2016/000416 filed on Jul. 7, 2016 which claims priority to Russian application RU2016116050 filed on Apr. 25, 2016.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15539882 | Jun 2017 | US |
| Child | 16150718 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16150718 | Oct 2018 | US |
| Child | 16285736 | US |
