Patent Application
20190143294
The present invention relates to a metal oxide-based chloride adsorbent with natural binder and a process for preparing the metal oxide-based chloride adsorbent.
The continuous catalytic reforming unit is one of the operation units in oil refinery and aromatic substance production facilities. The catalyst used in such process will act efficiently once activated with organic chloride, resulting in hydrogen, which is the by-product of such cracking unit, containing residual chloride compound in forms of inorganic chloride e.g. hydrogen chloride (HCl); and organic chloride e.g. vinyl chloride (VC) and trichloroethylene (TCE).
The chloride compound in such hydrogen gas stream is not only corrosive; it also impairs the efficiency of the catalyst in the downstream process of the oil refinery and aromatic substance production facilities. Thus the chloride compound has to be removed prior to the use of hydrogen gas in other operation units in the downstream process.
The current method for removing chloride compound in the hydrogen gas stream generated from the continuous catalytic reforming unit in the oil refinery and aromatic substance production facilities uses an operation unit of the fix bed adsorption column type.
There are 3 types of chloride adsorbent commonly used in petroleum or petro-chemical industry: chloride adsorbent on alumina support, zeolite-based chloride adsorbent and a metal oxide-based chloride adsorbent.
The first chloride adsorbent is chloride adsorbent having alumina as support and metal group 1 (alkaline metal) or metal group 2 (alkaline earth metal) of the Periodic Table as active component which will reacts with the chloride compound in hydrogen gas and thereby forming solid chloride compound attached to the adsorbent's surface. Example applications of such adsorbent can be found in the disclosures of U.S. Pat. No. 4,639,259, U.S. Pat. No. 5,316,998, U.S. Pat. No. 5,505,926 U.S. Pat. No. 5,935,894, U.S. Pat. No. 6,013,600, U.S. Pat. No. 6,200,544 B1, U.S. Pat. No. 7,758,837 B2 and a publication of US patent application no. 20100222215 A1. The above-mentioned chloride adsorbent having alumina as support, although efficient in absorbing inorganic chloride, still has a drawback since the released organic chloride e.g. vinyl chloride, organic chloride can undergo Friedel-Crafts alkylation reaction and become organic chloride complex, which causes fouling. In certain cases, the organic chloride released from the absorption column containing this type of chloride adsorbent is usually more concentrated than the organic chloride in the inlet gas stream of the absorption column.
The second chloride adsorbent is zeolite-based chloride adsorbent which is widely used for removing organic chloride e.g. vinyl chloride. Example applications of such adsorbent can be found in the disclosures of U.S. Pat. No. 4,762,537, U.S. Pat. No. 6,632,766 B2 and U.S. Pat. No. 8,551,328 B2.
The third chloride adsorbent is one prepared by extruding metal oxide with inorganic binder. Examples of such adsorbent are disclosed in the following patent documents.
U.S. Pat. No. 3,935,295 discloses chloride adsorbent obtained from mixing zinc oxide with calcium oxide, using clay as binder.
U.S. Pat. No. 4,721,824 discloses chloride adsorbent obtained from molding magnesium oxide using clay, silica, alumina and silica-alumina as binder.
Chloride adsorbent prepared by molding metal oxide using inorganic binder is further disclosed in patent no. JP-B-52-35036, U.S. Pat. No. 4,861,578, U.S. Pat. No. 5,688,479, U.S. Pat. No. 6,432,374 B1, and U.S. Pat. No. 9,156,738 B2 and TH patent no. 20248.
In the aforementioned metal oxide-based chloride adsorbent, inorganic binder is used at different proportions varying 1-20% by weight. Such inorganic binder will remain in the components of the metal oxide-based chloride adsorbent when used in operation, thereby decreasing the amount of metal oxide in the adsorbent which will absorb chloride.
The above patent documents demonstrate the efforts in developing different adsorbents that could minimize the remaining chloride compound in the hydrogen stream generated from the continuous catalytic reforming unit in the o aromatic substance production facilities.
The present invention relates to a process of preparing a metal oxide-based chloride adsorbent by extrusion using natural starch as organic binder and using program for maximizing the surface area of the adsorbent. The metal oxide-based chloride adsorbent, obtained from said process, wherein the natural starch and the porogen according to the present invention, is characterized in that it can be thermally degraded during the adsorbent preparation process. As a result, the metal oxide-based chloride adsorbent obtained from such process contains a higher quantitative proportion of metal oxide absorbing chloride.
The object of the present invention is to provide a process of preparing a metal oxide-based chloride adsorbent by extrusion using natural starch as organic binder and using porogen for maximizing the surface area of the adsorbent. Also provided is a metal oxide-based chloride adsorbent obtained from such process having a high quantitative proportion of metal oxide absorbing the chloride, especially for the case of the zinc oxide which is present in the chloride adsorbent prepared in an amount of up to 99.5 to 99.8% by weight. Such adsorbent is suitable for removing chloride compound in the hydrogen gas generated from the continuous catalytic reforming unit, which is one of the operations in an oil refinery and aromatic substance production facilities. The chloride adsorbent prepared according to the present invention has high chloride adsorption capacity as well as improved strength which will prevent breakage operation.
The present invention relates to a process of preparing a metal oxide-based chloride adsorbent by extrusion using starch as organic binder. The metal oxide-based chloride adsorbent according to the present invention is capable of removing chloride in hydrogen gas stream generated from a continuous catalytic reforming unit, wherein the components of the used in the process of preparing a metal oxide-based chloride adsorbent according to the present invention comprise:
In the process of preparing a metal oxide-based chloride adsorbent according to the present invention, the proportion of the components used are as follows:
Preferably, in the process of preparing a metal oxide-based chloride adsorbent according to the present invention, metal oxide powder is used, preferably, metal oxide of zinc.
Preferably, in the process of preparing a metal oxide-based chloride adsorbent according to the present invention, the metal oxide powder is smaller than 45 μm.
Preferably, in the process of preparing a metal oxide-based chloride adsorbent according to the present invention, the organic starch used is selected from glutinous rice starch, rice starch, cassava starch, corn starch or combinations of at least two of them.
Preferably, in the process of preparing a metal oxide-based chloride adsorbent according to the present invention, the porogen used is selected from polymethyl, methacrylate (PMMA) or carbon black.
Preferably, in the process of preparing a metal oxide-based chloride adsorbent according to the present invention, after the extrusion step, the paste product is of a cylindrical shape, preferably, a cylindrical shape having a diameter of 1-2 mm and a length of 3-4 mm.
Since the organic starch which is the binder and the porogen can be thermally degraded in the adsorbent preparation step of the above-mentioned process of preparing a metal oxide-based chloride adsorbent, the chloride adsorbent prepared according to the present invention consequently has high metal oxide, if zinc oxide is used, the amount of zinc oxide present in the chloride adsorbent will be as high as 99.5-99.8% by weight and capable of efficiently removing chloride compounds i.e. inorganic chloride e.g. hydrogen chloride and organic chloride e.g. vinyl chloride and trichloroethylene from the hydrogen stream in the operation of oil refinery and aromatic substance production facilities.
In a preferred embodiment, the metal oxide-based chloride adsorbent, obtained from the process of preparing a metal oxide-based chloride adsorbent according to the present invention, contain metal oxide of zinc in an amount of 99.5-99.8% by weight.
In a preferred embodiment, the metal oxide-based chloride adsorbent, obtained from the process of preparing a metal oxide-based chloride adsorbent according to the present invention, is of a cylindrical shape, preferably, the chloride adsorbent is of a cylindrical shape having a diameter of 1-2 mm and a length of 3-4 mm.
One or more embodiments of the present invention will be explained in more detail with reference to the following examples which, however, are not intended to limit the scope of one or more embodiments of the present invention.
Organic starch was mixed with distilled water at the defined proportion, at a controlled temperature of 80° C. to form gel. Metal oxide of zinc and porogen were then added and intimately mixed until a paste is formed.
The obtained paste product was extruded into cylindrical shape, preferably of a diameter of 1-2 mm and a length of 3-4 mm, left for 12 hours, then “oven-dried” to remove the remaining water by heating at the temperature of 100° C. for 1 hour at a heating rate of 3° C. per minute. The paste product was then “calcined to form pores” to increase porosity of the adsorbent. This step was carried out subsequent to the oven-drying step by calcination at the temperature of 800° C. for 4 hours at a heating rate of 3° C. per minute. Once finished pore forming by calcination, the resulting product was left to cool down to room temperature to obtain the metal oxide-based chloride adsorbent according to the present invention.
A commercial chloride adsorbent was used as a comparative example. Said adsorbent was chloride adsorbent on alumina support having the metal of group 1 of the Periodic Table i.e. sodium as active component.
The metal oxide-based chloride adsorbents of Example 1 and Example 2 were tested under the following condition.
The test under Condition 1 was carried out in the laboratory using a fix bed adsorption column having inorganic chloride therein i.e. the hydrogen chloride fed into the absorption column at a concentration in a range of 15-20 ppm, at a flow rate of 50 mL/minute, at a temperature of 25-28° C., a pressure of 1-2 bars. The height of all adsorbents contained in the absorption column was 10 cm. The column adsorbents were placed in 3 levels of the absorption column, each of which, in the order of upper to lower levels, has a height of 3, 3 and 4 cm. The inner diameter of the absorption column was 25.4 mm.
The test under Condition 2 was carried out in the of the actual operation condition in the refinery and aromatic substance production facilities using fix bed adsorption column having hydrogen stream from the cracking unit of naphtha and the catalyst was passed at GHSV (Gas Hourly Space Velocity) 1400 hours−1, a flow rate of 1 L per minute, at a temperature of 30-40° C., a pressure of 20-28 bars. The height of all adsorbents contained in the absorption column was 75 cm. The adsorbents were placed in 6 levels of the absorption column, each of which, in the order of upper to lower levels, has a height of 5, 5, 10, 20, 15 and 20 cm The inner diameter of the absorption column was 38 mm.
The chloride adsorbent tests were conducted in a continuous manner in both conditions above. The commercial chloride adsorbent was used as a comparative example. The concentration of the inorganic chloride e.g. hydrogen chloride and the organic chloride (for Condition 2) e.g. vinyl chloride gas and trichloroethylene gas was measure both at the inlet (initial concentration (Co) in part per million (ppm)) and the outlet (concentration at any time points (C) in ppm) of the absorption column. Throughout the test, in order to determine the breakthrough time (BT) which refers to the time at which the concentration of the chloride compound in the outlet gas exceeds 1 ppm which exceeds the acceptable value for oil refinery and aromatic substance production facilities.
Once the test was finished, the tested adsorbents were analyzed for the amount of the absorbed chloride, the Loss of Drying (LOD) of the tested adsorbent, and the crushing strength of the adsorbent.
The chloride adsorbent test was carried out in a continuous manner under the above-indicated condition in the laboratory. The chloride adsorbents according to the present invention (Example 1) and the comparative Example (Example 2) were tested in the presence of hydrogen chloride, fed into the absorption column (Co), having the concentration range of 5000 ppm. The results are shown in Table 1. The chloride adsorbent of Example 1 was found to have greater pre-test crushing strength and greater efficiency than Example 2 based on the fact that the chloride adsorbent of Example 1 has a higher percentage by weight of the absorbed chloride than Example 2. The breakthrough time of hydrogen chloride was also longer than Example 2.
The chloride adsorbent test was carried out in the actual operation condition in the aromatic substance production facility e.g. for benzene, toluene, and xylene as mentioned above. The chloride adsorbents of Example 1 and Example 2 were tested at a fed hydrogen chloride concentration range of 10-20 ppm, and fed vinyl chloride gas concentration range of 0-5 ppm and a fed trichloroethylene gas concentration range of 2-10 ppm. The results are shown in Table 2. The chloride adsorbent of Example 1 was found to have a greater pre-test and post-test crushing strength as well as greater efficiency in absorbing chloride than Example 2 based on the fact that the absorbed chloride content of Example 1 was greater than that of Example 2. The breakthrough time of the three chloride gases i.e. hydrogen chloride gas, vinyl chloride gas, and trichloroethylene gas was also longer than that of Example 2.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1601004158 | Jul 2016 | TH | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/TH2016/000099 | 12/20/2016 | WO | 00 |
