Modified activated carbon preparation and methods thereof

Patent metadata

Field	Value
Publication number	US-2017113202-A1
Application number	US-201514920290-A
Country	US
Kind code	A1
Filing date	Oct 22, 2015
Priority date	Oct 22, 2015
Publication date	Apr 27, 2017
Grant date	—

Abstract

A process for making a modified, mesoporous activated carbon material from waste oil fly ash. The process involves a physicochemical treatment of a raw waste oil fly ash sample, where the sample is initially refluxed in an acid solution, then activated at about 1000° C. and in the presence of carbon dioxide. The activated carbon may be further functionalized with carboxylic and/or amine groups by refluxing the activated carbon in a second acid solution and/or an ammonia solution. The activated carbon, as prepared, has a BET surface area of 30-400 m 2 /g, a total pore volume of 0.25-0.50 cm 3 /g and an average pore size of 40-100 Å. A method for removing hydrogen sulfide from natural gas with the modified activated carbon is also provided.

First claim

1 . A process for preparing an activated carbon material, comprising:
refluxing a waste oil fly ash powder with a first acid solution to form a solid residue; and heating the solid residue at 900-1050° C. and purging the solid residue in a flow of carbon dioxide to form the activated carbon material.

2 . The process of claim 1 , wherein the first acid solution comprises one or more acids selected from the group consisting of sulfuric acid, nitric acid and phosphoric acid.

3 . The process of claim 2 , wherein the first acid solution comprises two acids at a volume ratio of 1-13:1-13.

4 . The process of claim 2 , wherein the first acid solution comprises three acids at a volume ratio of 1-8.5:1-8.5:1-8.5.

5 . The process of claim 1 , wherein the refluxing is carried at 100-150° C. for 3-6 h and at a concentration of 10-100 g of the waste oil fly ash powder per liter of the first acid solution.

6 . The process of claim 1 , wherein the heating is carried out for 30-90 min.

7 . The process of claim 1 , wherein the purging is carried out for 15-45 min, at 1-5 bar and at a carbon dioxide flow rate of 0.5-2.0 L/min.

8 . The process of claim 1 , wherein during the purging, the solid residue is not chemically modified.

9 . The process of claim 1 , wherein the solid residue has a pH value of 5.5-7.5.

10 . The process of claim 1 , further comprising:
contacting and refluxing the activated carbon material with a second acid solution or an ammonia solution to attach carboxylic groups or amine groups onto the surface of the activated carbon material.

11 . The process of claim 10 , wherein the second acid solution is a nitric acid solution.

12 . The process of claim 10 , wherein the contacting and the refluxing are carried out at 80-120° C. for 3-6 h and at a concentration of 50-200 g of the activated carbon material per liter of the second acid solution or the ammonia solution.

13 . The process of claim 1 , wherein the refluxing, the heating and the purging increase the BET surface area of the activated carbon material, increase the total pore volume of the activated carbon material and reduce the average pore size of the activated carbon material.

14 . An activated carbon material prepared by the process of claim 1 , wherein the activated carbon material has a BET surface area of 30-400 m 2 /g, a total pore volume of 0.25-0.50 cm 3 /g and an average pore size of 40-100 Å.

15 . A method for removing hydrogen sulfide from a gaseous stream, comprising:
contacting the gaseous stream with the activated carbon material of claim 14 .

16 . The method of claim 15 , wherein the gaseous stream is a natural gas stream.

17 . The method of claim 15 , wherein the activated carbon material has a concentration of 0.01-0.05 g per ppm of the hydrogen sulfide present in the gaseous stream.

18 . The method of claim 15 , wherein the activated carbon material is affixed to a packed bed of an adsorption column and the gaseous stream is passed through the packed bed at 0.1-1.0 L/min at atmospheric pressure and at ambient temperature.

19 . The method of claim 15 , wherein the activated carbon material adsorbs the hydrogen sulfide and has a hydrogen sulfide adsorption capacity of 0.10-0.35 mg of hydrogen sulfide per gram of the activated carbon material.

20 . The method of claim 15 , wherein the activated carbon material has a regeneration efficiency of 40-90%.

Assignees

• Univ King Fahd Pet & Minerals

Inventors

• Shawabkeh Reyad Awwad
• Hussein Ibnelwaleed Ali
• ASLAM Hafiz Muhammad Zaheer
• Al-Baghli Nadhir H

Classifications

• B01D2257/304

  Hydrogen sulfide · CPC title

• B01D53/02

  by adsorption, e.g. preparative gas chromatography {(solid sorbent compositions B01J20/00, preparation of inorganic compounds or elements C01)} · CPC title

• C01B31/12

  Chemistry & Metallurgy · mapped topic

• B01J20/3078

  Thermal treatment, e.g. calcining or pyrolizing · CPC title

• B01J20/20 Primary

  comprising free carbon; comprising carbon obtained by carbonising processes · CPC title