Patent Application
20110256039
1. Field of the Invention
This invention relates to a method for regenerating amorphous iron oxide hydroxide after being used as desulfurizer and composition comprising amorphous iron oxide hydroxide after being used as desulfurizer.
2. Description of the Related Art
In the existing technologies especially in industrial application, it is rarely studied of preparation and regeneration of amorphous iron oxide hydroxide. and no regeneration or regeneration method of amorphous FeOOH is published.
However, some research is still in the laboratory of exploration stage. Regeneration of amorphous iron oxide hydroxide is very slow and lasts a long time in natural state. Therefore, the process is unsuitable for fast and mass production.
One vital objective of this study is to achieve the mass regeneration of amorphous iron oxide hydroxide after used in industrial production. If this point comes true it will be a great revolution in desulfurizer field and the followed shortcomings of the existing desulfurizer can be eliminated. Conventional desulfurizers cannot be regenerated (or regeneration is costly) so that large quantities of waste product must be buried. The technology not only wastes resources but also pollutes the environment.
In view of the above-described problems, it is one objective of the invention to provide a method for regenerating amorphous iron oxide hydroxide after being used as a desulfurizer that is suitable for fast and mass production.
It is another objective of the invention to provide a method for regenerating the high concentration composition of the amorphous iron oxide hydroxide after being used as a desulfurizer.
To achieve the above objectives, in accordance with one embodiment of the invention, a method is provided for regenerating amorphous iron oxide hydroxide after being used as a desulfurizer. The method comprises the steps of:
Desulfurization and regeneration of the amorphous iron oxide hydroxide react according to the chemical reaction: 2FeOOH+3H2S→Fe2S3.H2O+3H2O, Fe2S3.H2O+3/202→2FeOOH+3S.
In a class of this embodiment, prior to grinding the waste mixture is washed with water. after step (3) the floated elemental sulfur is separated. The weight proportion of solid in the suspension prepared of step (2) is 5-30%, particularly 10-15%. The gas containing oxygen is air in step (2). In step (3), an auxiliary agent is added to the reactor to accelerate the floating and separation of the elemental sulfur. The auxiliary agent is water glass and kerosene. The container in step (3) is flotation tank. The waste mixture is ground into particles of size 100-400 mesh in step (1), particularly 200 mesh.
In a class of this embodiment, the method is applied to regeneration of a composition used amorphous iron oxide hydroxide as active ingredient after the composition is used as desulfurizer.
This invention provides a method of regenerating amorphous iron oxide hydroxide after being used as a desulfurizer, the method of comprising the following steps:
In a class of embodiment, prior to grinding, the waste mixture is washed with water. The elemental sulfur is separated after the extracting solvent is concentrated. The weight proportion of solid in the suspension prepared of step (b) is 5-30%, particularly 10-15%. The gas containing oxygen is air in step (b). The solvent is non polar solvent in step (c). The non-polar solvent is carbon tetrachloride or carbon disulfide. The waste mixture is ground into particles of size 100-400 mesh in step (a), particularly 200 mesh.
In a class of this embodiment, the method is applied to regeneration of a composition used amorphous iron oxide hydroxide as active ingredient after the composition is used as desulfurizer.
Comparing with existing technology, the advantages of the invention are summarized below:
To illustrate the invention, experiments detailing the method for preparing a composition comprising amorphous iron oxide hydroxide, a desulfurizer, and a preparation method thereof, as well as a desulfurizer regeneration method, are described below. It should be noted that the following examples are intended to describe and not to limit the invention.
The process for preparing amorphous iron oxide hydroxide comprises the following steps:
Solid Fe(NO3)2.6H2O was prepared into solution and placed in reaction tank and then solid NaOH was put into the reaction tank and the mixture was stirred simultaneously. The reaction temperature was kept at 30-40° C. through controlling the speed of feeding NaOH and the pH value of mixed solution reached 7.5 at the end of reaction. Then the solution was filtered and filter cake was washed until the weight proportion of Na+ in the filter cake less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 10%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+/Fet less than 1%. Then the solution was filtered and the resultant solid was dried at 80° C. to yield a composition comprising amorphous iron oxide hydroxide (composition A). In the composition, the weight percent of amorphous iron oxide hydroxide was 100%, with a sulfur capacity of 62%.
Fet in this example was the total content of elemental Ferrum. Fe2+/Fet was analysed through phenanthroline spectrophotometry. The content of Na+ was analysed through flame spectrometry. The following examples are the same.
The content of solid hydroxide or the ratio of two materials was controlled through controlling the pH value of solution in this example. The following examples are the same.
The process for regeneration of the composition A after being used for desulfurization was described as below:
Composition A was added to a desulfurization reactor. After H2S passing through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders with a particle size of 300 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 15%, compressed air was charged into the suspension, and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to have been completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was filtered to yield a solid. The solid was added to a flotation tank. Water was added, and water glass and kerosene were added as auxiliary agents, and air was charged into the slurry. Due to hydrophobicity, the elemental sulfur was removed by overflowing the tank. The precipitate in the bottom of the tank was a composition comprising amorphous iron oxide hydroxide. The composition was roasted and could be reused as a desulfurizer. The composition had a sulfur capacity of 59%. After second, third, and fourth rounds of regeneration, the composition had a sulfur capacity of 58%, 56%, and 54%, respectively.
The auxiliary agent was helpful for floatation of elemental sulfur, separating amorphous iron oxide hydroxide and elemental sulfur well. Following examples was the same.
The process for preparing the composition containing amorphous iron oxide hydroxide comprises the following steps:
152 g solid FeSO47H2O was prepared into solution and placed in reaction tank and then 45 g NaOH solid was put into the reaction tank and the mixture was stirred simultaneously. Reaction temperature was kept not exceeding 50° C. through controlling the speed of feeding NaOH. After the reaction, the solution was filtered and filter cake was washed until the weight proportion of Na+ in the filter cake less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 30%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+/Fet less than 1%. Then the solution was filtered and the resultant solid was dried at 90° C. to yield a composition comprising amorphous iron oxide hydroxide (composition B). In the composition, the weight percent of amorphous iron oxide hydroxide was 85% and the other ingredients comprised NaSO4, water, and TiO2 (TiO2 is impurity in FeSO4.7H2O, the following examples are the same), with a sulfur capacity of 53%.
The process for regeneration of the composition B after being used for desulfurization was described as below:
Composition B was added to a desulfurization reactor. After H2S passing through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders with a particle size of 100 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 5%, compressed air was charged into the suspension, and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to have been completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was added to a flotation tank. Water were added, and air was charged into the slurry. Due to hydrophobicity, the elemental sulfur was removed by overflowing the tank. The precipitate in the bottom of the tank was a composition comprising amorphous iron oxide hydroxide. The composition was roasted and could be reused as a desulfurizer. The composition had a sulfur capacity of 52%. After second, third, and fourth rounds of regeneration, the composition had a sulfur capacity of 50%, 48%, and 46%, respectively.
The process for preparing the composition containing amorphous iron oxide hydroxide comprises the following steps:
127 g FeCl2.4H2O was prepared into solution and placed in reaction tank and then 72 g solid KOH was put into the reaction tank and the mixture was stirred simultaneously. The reaction temperature was kept not exceeding 50° C. through controlling the speed of feeding KOH. After the reaction, the solution was filtered and filter cake was washed until the weight proportion of K+ in the filter cake was less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 15%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+/Fet was less than 1%. Then the solution was filtered and the resultant solid was dried at 100° C. to yield a composition comprising amorphous iron oxide hydroxide (composition C). In the composition, the weight percent of amorphous iron oxide hydroxide was 81% and the other ingredients comprised KCl, water and impurity unknown, with a sulfur capacity of 50%. The content of K+ was analysed through flame spectrometry. The following examples are the same.
The process for regeneration of the composition C after being used for desulfurization is described as below:
Composition C was added to a desulfurization reactor. After H2S passing through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders with a particle size of 200 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 10%, compressed air was charged into the suspension, and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to have been completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was added to a flotation tank. Water was added, and water glass and kerosene were added as auxiliary agents, and air was charged into the slurry. Due to hydrophobicity, the elemental sulfur was removed by overflowing the tank. The precipitate in the bottom of the tank was a composition comprising amorphous iron oxide hydroxide. The composition was roasted and could be reused as a desulfurizer. The composition had a sulfur capacity of 48%. After second, third, and fourth rounds of regeneration, the composition had a sulfur capacity of 46.5%, 45%, and 44%, respectively.
The process for preparing the composition containing amorphous iron oxide hydroxide comprises the following steps:
Solid FeCl2 was prepared into solution and placed in reaction tank and then solid Ca(OH)2 was put into the reaction tank and the mixture was stirred simultaneously. The reaction temperature was kept at 40-50° C. through controlling the speed of feeding Ca(OH)2 and pH value of mixed solution is 8 at the end of reaction. Then the solution was filtered and filter cake was washed until the weight proportion of Cl− in the filter cake less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 5%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+ /Fet less than 1%. Then the solution was filtered and the resultant solid was dried at 70° C. to yield a composition comprising amorphous iron oxide hydroxide (composition D). In the composition, the weight percent of amorphous iron oxide hydroxide was 92% and the other ingredients comprised CaCl2 and water, with a sulfur capacity of 57%. Wherein, the content of Cl− was analysed through mercuric thiocyanate colorimetry.
The process for regeneration of the composition D after being used for desulfurization was described as below:
Composition D was added to a desulfurization reactor. After H2S passing through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders with a particle size of 400 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 30%, compressed air was charged into the suspension, and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to have been completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was filtered to yield a solid. The solid was added to a flotation tank. Water was added, and water glass and kerosene were added as auxiliary agents, and air was charged into the slurry. Due to hydrophobicity, the elemental sulfur was removed by overflowing the tank. The precipitate in the bottom of the tank was a composition comprising amorphous iron oxide hydroxide. The composition was roasted and could be reused as a desulfurizer. The composition had a sulfur capacity of 55%. After second, third, and fourth rounds of regeneration, the composition had a sulfur capacity of 54%, 52%, and 50%, respectively.
The process for preparing the composition containing amorphous iron oxide hydroxide comprises the following steps:
Solid Fe(NO3)2.6H2O was prepared into solution and placed in reaction tank and then solid KOH was put into the reaction tank and the mixture was stirred simultaneously. Reaction temperature was kept at 50-60° C. through controlling the speed of feeding KOH and pH value of mixed solution is 8 at the end of reaction. Then the solution was filtered and filter cake was washed until the weight proportion of K+ in the filter cake less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 12%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+ /Fet was less than 1%. Then the solution was filtered and the resultant solid was dried at 50° C. to yield a composition comprising amorphous iron oxide hydroxide(composition E).
500 g composition comprising amorphous iron oxide hydroxide, 35 g sesbania powder as binder and 20 g sawdust as additive were mixed uniformly, kneaded with appropriate quantities of water using a small kneader, and extruded using a small twin screw extruder to yield a strip. The desulfurizer was roasted at 80° C. for 4 h, and the sulfur capacity thereof was measured to be 47%. The desulfurizer was named desulfurizer E.
The process for regeneration of the composition E after being used for desulfurization was described as below:
The desulfurizer E was added to a desulfurization reactor. After H2S passing through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders of particle size 200 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 15%. Compressed air was charged into the slurry and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to have been completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was placed in a flotation tank, water was added, and air was charged. The elemental sulfur, sesbania powder and sawdust were removed, together with excess air, by overflowing the tank. The precipitate in the bottom of the tank was a composition comprising amorphous iron oxide hydroxide. The composition comprising amorphous iron oxide hydroxide was roasted at 70° C., and sesbania powder and sawdust were added according to the proportions described above. The mixture was treated in accordance with the method and reaction conditions described above to yield a new desulfurizer (desulfurizer E′) with a sulfur capacity of 46%.
The desulfurizer E′ was used to desulfurize and was regenerated according to the process described for the desulfurizer E. A new desulfurizer (desulfurizer E″) with a sulfur capacity of 44% was obtained.
After three rounds of desulfurizing and regenerating, the fourth desulfurizer generated (desulfurizer E′″) had a sulfur capacity of 42%.
After four rounds of desulfurizing and regenerating, the fifth desulfurizer generated (desulfurizer E″″) had a sulfur capacity of 40%.
The process for preparing the composition containing amorphous iron oxide hydroxide comprises the following steps:
Solid FeSO4.7H2O was prepared into solution and placed in reaction tank and then solid NaOH was put into the reaction tank and the mixture was stirred simultaneously. Reaction temperature was kept not exceeding 50° C. through controlling the speed of feeding NaOH and pH value of mixed solution is 8 at the end of reaction. Then the solution was filtered and filter cake was washed until the weight proportion of Na+ in the filter cake less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 20%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+ /Fet was less than 1%. Then the solution was filtered and the resultant solid was dried at 40° C. to yield a composition comprising amorphous iron oxide hydroxide (composition F).
500 g composition F comprising amorphous iron oxide hydroxide, 35 g sesbania powder as binder and 20 g rice hull powder as additive were mixed uniformly, kneaded with appropriate quantities of water using a small kneader, and extruded using a small twin screw extruder to yield a strip. The desulfurizer was roasted at 70° C. for 6 h, and the sulfur capacity thereof was measured to be 45%. The desulfurizer was named desulfurizer F.
The process for regeneration of the composition F after being used for desulfurization was described as below:
The desulfurizer F was added to a desulfurization reactor. After H2S passing through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders of particle size 200 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 25%. Compressed air was charged into the slurry and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to have been completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was placed in a flotation tank, water was added, and air was charged. The elemental sulfur, cellulose powder and rice hull powder were removed, together with excess air, by overflowing the tank. The precipitate in the bottom of the tank was a composition comprising amorphous iron oxide hydroxide. The composition comprising amorphous iron oxide hydroxide was roasted at 80° C., and cellulose powder and rice hull powder were added according to the proportions described above. The mixture was treated in accordance with the method and reaction conditions described above to yield a new desulfurizer (desulfurizer F′) with a sulfur capacity of 44%.
The desulfurizer F′ was used to desulfurize and was regenerated according to the process described for the desulfurizer F. A new desulfurizer (desulfurizer F″) with a sulfur capacity of 42.5% was obtained.
After three rounds of desulfurizing and regenerating, the fourth desulfurizer generated (desulfurizer F′″) had a sulfur capacity of 40%.
After four rounds of desulfurizing and regenerating, the fifth desulfurizer generated (desulfurizer F″″) had a sulfur capacity of 38%.
The process for preparing the composition containing amorphous iron oxide hydroxide comprises the following steps:
Solid Fe(NO3)2.6H2O was prepared into solution and placed in reaction tank and then solid NaOH was put into the reaction tank and the mixture was stirred simultaneously. Reaction temperature was kept at 30-40° C. through controlling speed of the feeding NaOH and pH value of mixed solution reached 7.5 at the end of reaction. Then the solution was filtered and filter cake was washed until the weight proportion of Na+ in the filter cake less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 10%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+ /Fet was less than 1%. Then the solution was filtered and the resultant solid was dried at 80° C. to yield a composition comprising amorphous iron oxide hydroxide (composition G). In the composition, the weight percent of amorphous iron oxide hydroxide was 100%, with a sulfur capacity of 62%.
Fet in this example is the total content of elemental Ferrum. Fe2+ /Fet was analysed through phenanthroline spectrophotometry. The content of Na+ was analysed through flame spectrometry. The following examples are the same.
The content of hydroxide solid or the ratio of two materials is controlled through controlling the pH value of solution in this example. The following examples are the same.
The process for regeneration of the composition G after being used for desulfurization was described as below:
The desulfurizer G was added to a desulfurization reactor. After H2S passing through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders of particle size 300 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 15%. Compressed air was charged into the suspension and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to have been completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was filtered to yield a solid that was extracted thrice with CCl4. The extract was combined and distilled to yield crystallized elemental sulfur. The solid remaining after extraction was a composition comprising amorphous iron oxide hydroxide. The composition was roasted and could be reused as a desulfurizer. The composition had a sulfur capacity of 59%. After second, third, and fourth rounds of regeneration, the composition had a sulfur capacity of 58%, 56%, and 54%, respectively.
The process for preparing the composition containing amorphous iron oxide hydroxide comprises the following steps:
152 g solid FeSO4.7H2O solid was prepared into solution and placed in reaction tank and then 45 g solid NaOH solid was put into the reaction tank and the mixture was stirred simultaneously. Reaction temperature was kept not exceeding 50° C. through controlling speed of feeding NaOH. After the reaction, the solution was filtered and filter cake was washed until the weight proportion of Na+ in the filter cake less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 30%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+ /Fet less than 1%. Then the solution was filtered and the resultant solid was dried at 90° C. to yield a composition comprising amorphous iron oxide hydroxide (composition H). In the composition, the weight percent of amorphous iron oxide hydroxide was 85% and the other ingredients comprised NaSO4, water, and TiO2 (TiO2 is impurity in FeSO4.7H2O, the following examples are the same), with a sulfur capacity of 53%.
The process for regeneration of the composition H after being used for desulfurization was described as below:
To a desulfurization reactor was added composition H. After passing H2S through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders of particle size 100 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 5%. Compressed air was charged into the suspension and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to have completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was filtered to yield a solid that was extracted thrice with CCl4. The extract was combined and distilled to yield crystallized elemental sulfur. The solid remaining after extraction was a composition comprising amorphous iron oxide hydroxide. The composition was roasted and could be reused as a desulfurizer. The composition had a sulfur capacity of 50%. After second, third, and fourth rounds of regeneration, the composition had a sulfur capacity of 48%, 46%, and 44%, respectively.
The process for preparing the composition containing amorphous iron oxide hydroxide comprises the following steps:
127 g FeCl2.4H2O was prepared into solution and placed in reaction tank and then 72 g solid KOH solid was put into the reaction tank and the mixture was stirred simultaneously. Reaction temperature was kept not exceeding 50° C. through controlling speed of feeding KOH. After the reaction, the solution was filtered and filter cake was washed until the weight proportion of K+ in the filter cake less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 15%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+ /Fet less than 1%. Then the solution was filtered and the resultant solid was dried at 100° C. to yield a composition comprising amorphous iron oxide hydroxide (composition I). In the composition, the weight percent of amorphous iron oxide hydroxide was 81% and the other ingredients comprised KCl, water and impurity unknown, with a sulfur capacity of 50%. The content of K+ was analysed through flame spectrometry. The following examples are the same.
The process for regeneration of the composition I after being used for desulfurization was described as below:
The desulfurizer I was added to a desulfurization reactor. After H2S passing through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders of particle size 200 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 10%. Compressed air was charged into the suspension and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to have completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was filtered to yield a solid that was extracted thrice with CS2. The extract was combined and distilled to yield crystallized elemental sulfur. The solid remaining after extraction was a composition comprising amorphous iron oxide hydroxide. The composition was roasted and could be reused as a desulfurizer. The composition had a sulfur capacity of 48%. After second, third, and fourth rounds of regeneration, the composition had a sulfur capacity of 46%, 44.5%, and 42%, respectively.
The process for preparing the composition containing amorphous iron oxide hydroxide comprises the following steps:
Solid FeCl2 solid was prepared into solution and placed in reaction tank and then Ca(OH)2 solid was put into the reaction tank and the mixture was stirred simultaneously. Reaction temperature was kept at 40-50° C. through controlling the speed of feeding Ca(OH)2 and pH value of mixed solution is 8 at the end of reaction. Then the solution was filtered and filter cake was washed until the weight proportion of Cl− in the filter cake was less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 5%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+ /Fet less than 1%. Then the solution was filtered and the resultant solid was dried at 70° C. to yield a composition comprising amorphous iron oxide hydroxide (composition J). In the composition, the weight percent of amorphous iron oxide hydroxide was 92% and the other ingredients comprised CaCl2 and water, with a sulfur capacity of 57%. Wherein, the content of Cl− was analysed through mercuric thiocyanate colorimetry.
The process for regeneration of the composition J after being used for desulfurization was described as below:
The desulfurizer J was added to a desulfurization reactor. After H2S passing through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders of particle size 400 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 30%. Compressed air was charged into the suspension and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to have completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was filtered to yield a solid that was extracted thrice with CS2. The extract was combined and distilled to yield crystallized elemental sulfur. The solid remaining after extraction was a composition comprising amorphous iron oxide hydroxide. The composition was roasted and could be reused as a desulfurizer. The composition had a sulfur capacity of 55%. After second, third, and fourth rounds of regeneration, the composition had a sulfur capacity of 53%, 50%, and 48%, respectively.
The process for preparing the composition containing amorphous iron oxide hydroxide comprises the following steps:
Solid Fe(NO3)2.6H2O solid was prepared into solution and placed in reaction tank and then solid KOH solid was put into the reaction tank and the mixture was stirred simultaneously. Reaction temperature was kept at 50-60° C. through controlling speed of feeding KOH and pH value of mixed solution is 8 at the end of reaction. Then the solution was filtered and filter cake was washed until the weight proportion of K+ in the filter cake less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 12%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+ /Fet less than 1%. Then the solution was filtered and the resultant solid was dried at 50° C. to yield a composition comprising amorphous iron oxide hydroxide(composition K).
500 g composition K comprising amorphous iron oxide hydroxide, 35 g sesbania powder as binder and 20 g sawdust as additive were mixed uniformly, kneaded with appropriate quantities of water using a small kneader, and extruded using a small twin screw extruder to yield a strip. The desulfurizer was roasted at 80° C. for 4 h, and the sulfur capacity thereof was measured to be 47%. The desulfurizer was named desulfurizer K.
The process for regeneration of the composition K after being used for desulfurization was described as below:
The desulfurizer K was added to a desulfurization reactor. After H2S passing through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders of particle size 200 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 15%, compressed air was charged, and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to be completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was filtered to yield a solid that was extracted thrice with CCl4. The extract was combined and distilled to yield crystallized elemental sulfur. The remaining solid after extraction was a composition comprising amorphous iron oxide hydroxide. The composition comprising amorphous iron oxide hydroxide was roasted at 70° C., and sesbania powder and sawdust were added according to the proportions described above. The mixture was treated according to the method and reaction conditions described above to yield a new desulfurizer (desulfurizer K′) with a sulfur capacity of 45%.
The desulfurizer K′ was used for desulfurization and was regenerated according to the process described for the regeneration of desulfurizer K. A new desulfurizer (desulfurizer K″) with a sulfur capacity of 43% was thereby obtained.
After three rounds of desulfurizing and regenerating, the fourth desulfurizer generated (desulfurizer K′″) had a sulfur capacity of 38.5%.
After four rounds of desulfurizing and regenerating, the fifth desulfurizer generated (desulfurizer K″″) had a sulfur capacity of 35.5%.
The process for preparing the composition containing amorphous iron oxide hydroxide comprises the following steps:
Solid FeSO4.7H2O solid was prepared into solution and placed in reaction tank and then solid NaOH solid was put into the reaction tank and the mixture was stirred simultaneously. Reaction temperature was kept not exceeding 50° C. through controlling speed of feeding NaOH and pH value of mixed solution is 8 at the end of reaction. Then the solution was filtered and filter cake was washed until the weight proportion of Na+ in the filter cake less than 0.5%. The filter cake was prepared into suspension, in which the weight proportion of solid is 20%. Then air was fed into the suspension for oxidation until the weight proportion of Fe2+ /Fet was less than 1%. Then the solution was filtered and the resultant solid was dried at 40° C. to yield a composition comprising amorphous iron oxide hydroxide(composition L).
500 g composition L comprising amorphous iron oxide hydroxide, 35 g sesbania powder as binder and 20 g rice hull powder as additive were mixed uniformly, kneaded with appropriate quantities of water using a small kneader, and extruded using a small twin screw extruder to yield a strip. The desulfurizer was roasted at 70° C. for 6 h, and the sulfur capacity thereof was measured to be 45%. The desulfurizer was named desulfurizer L.
The process for regeneration of the composition L after being used for desulfurization was described as below:
The desulfurizer L was added to a desulfurization reactor. After H2S passing through the reactor, the resultant waste mixture was washed with water and ground in the presence of water using a wet ball mill into powders of particle size 200 mesh. An aqueous suspension of the powders was prepared with a solid weight percent of 25%, compressed air was charged, and a sample was collected for testing. When no H2S was produced from the reaction between the sample and hydrochloric acid, the iron sulfide in the suspension was determined to be completely transformed into a slurry comprising amorphous iron oxide hydroxide and elemental sulfur. The slurry was filtered to yield a solid that was extracted thrice with CS2. The extract was combined and distilled to yield crystallized elemental sulfur. The remaining solid after extraction was a composition comprising amorphous iron oxide hydroxide. The composition comprising amorphous iron oxide hydroxide was roasted at 80° C., and cellulose powder and rice hull powder were added according to the proportions described above. The mixture was treated according to the method and reaction conditions described above to yield a new desulfurizer (desulfurizer L′) with a sulfur capacity of 43%.
The desulfurizer L′ was used for desulfurization and was regenerated according to the process described for the regeneration of desulfurizer L. A new desulfurizer (desulfurizer L″) with a sulfur capacity of 42% was thereby obtained.
After three rounds of desulfurizing and regenerating, the fourth desulfurizer generated (desulfurizer L′″) had a sulfur capacity of 40%.
After four rounds of desulfurizing and regenerating, the fifth desulfurizer generated (desulfurizer L″″) had a sulfur capacity of 37.5%.
In the above mentioned examples, the sulfur capacity measured using a standard gas containing 40000 ppm H2S at normal temperature (−5° C. to 45° C.) and normal pressure (generally, one atmosphere pressure). Specifically, sulfur was quantitatively measured using WK-2C integrated microcoulometer (manufactured by Jiangsu Electroanalytical Instrument Factory), which had a minimal measurement volume of 0.2 ppm.
The embodiments of the invention have showed that the regeneration method is suitable for both pure amorphous iron oxide hydroxide and amorphous iron oxide hydroxide of high purity. However, it is of little significance for composition comprising amorphous iron oxide hydroxide lower than 40% in weight content, which has impurity and low desulfurization capacity after regenerating. Additionally, the regeneration method in the invention is suitable for any other desulfurizer comprising amorphous iron oxide hydroxide besides desulfurizer comprising amorphous iron oxide hydroxide, binder and additive in embodiments.
While particular embodiments of the invention have been shown and described, it will be obvious to those skilled in the art that changes and modifications may be made without departing from the invention in its broader aspects, and therefore, the aim in the appended claims is to cover all such changes and modifications that fall within the true spirit and scope of the invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 200810247538.7 | Dec 2008 | CN | national |
| 200810247539.1 | Dec 2008 | CN | national |
This application is a continuation of International Patent Application No. PCT/CN2009/001598, with an international filing date of Dec. 30, 2009, designating the United States, now pending, and further claims priority benefits to Chinese Patent Application No. 200810247539.1, filed Dec. 30, 2008 and Chinese Patent Application No. 200810247538.7, filed on Dec. 30, 2008. The contents of all of the aforementioned applications, including any intervening amendments thereto, are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/CN2009/001598 | Dec 2009 | US |
| Child | 13172893 | US |
