2010
DOI: 10.1016/j.biombioe.2009.12.020
|View full text |Cite
|
Sign up to set email alerts
|

Preparation and characterization of activated carbon from rubber-seed shell by physical activation with steam

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

3
84
0
3

Year Published

2011
2011
2023
2023

Publication Types

Select...
7
1
1

Relationship

1
8

Authors

Journals

citations
Cited by 154 publications
(90 citation statements)
references
References 16 publications
3
84
0
3
Order By: Relevance
“…In principle, the activation methods of preparing activated carbons can be divided into two categories: chemical activation and physical activation. 4 In physical activation, a raw material is first carbonized, and the resulting char is secondarily activated under a flow of suitable gas such as steam, carbon dioxide, air or their mixtures. [5][6][7] In chemical activation, the raw material is impregnated with an activation reagent like H 3 PO 4 , KOH, ZnCl 2 or their mixtures.…”
Section: Introductionmentioning
confidence: 99%
“…In principle, the activation methods of preparing activated carbons can be divided into two categories: chemical activation and physical activation. 4 In physical activation, a raw material is first carbonized, and the resulting char is secondarily activated under a flow of suitable gas such as steam, carbon dioxide, air or their mixtures. [5][6][7] In chemical activation, the raw material is impregnated with an activation reagent like H 3 PO 4 , KOH, ZnCl 2 or their mixtures.…”
Section: Introductionmentioning
confidence: 99%
“…The initial adsorptive value of P200/300/400/500-0.25-750 in Fig. 1 was 301-321 cm 3 /g, and as the relative pressure P/P 0 increased, the adsorption volume rising slope was larger than 0.25-750, meaning pore size distribution was wide. In addition, as the nitrogen adsorption-desorption isotherms are plain shaped under high relative pressure, when the P/P 0 approaches saturation, the isotherm trailing increases sharply [18], [50], [67], thus, it can be regarded as the result of limited nitrogen adsorption, meaning the adsorbate implements capillary condensation in mesopores, namely, the proportion of mesopores of the ACs is increased.…”
Section: B Adsorption-desorption Isothermsmentioning
confidence: 90%
“…The activation methods for preparing activated carbons (ACs) can be divided into physical and chemical activation methods; physical activation carbonizes the precursor, and uses the activated gas for activation at high temperature [1]- [3]; chemical activation uses a chemical activating agent to dehydrate and oxidize the precursor, and simultaneously proceeds with carbonization and activation at a low temperature. The activating agents are mostly strong acid, strong base, or alkali earth containing metallics; some can erode, melt, or dehydrate the precursor and equipment, while Manuscript received May 16, 2017; revised July 31, 2017.…”
Section: Introductionmentioning
confidence: 99%
“…uniform composition, high carbon yield and low ash content) compared to the ACs prepared from the natural feedstock [12,13]. During the production of ACs, carbonization of a raw material, performed in the temperature range of 600-900°C under an inert atmosphere, is often followed by physical activation (for example, treatment with steam or CO 2 ) and/or chemical activation (for example, reaction with KOH, ZnCl 2 or H 3 PO 4 ), resulting in a development of surface area and pore volume of formed ACs as well as changes in their surface composition [14][15][16][17][18][19][20]. A majority of ACs is microporous solids with very narrow channels, which can cause diffusion limitations restricting an access to inner adsorption centres and making ACs unregenerable [21][22][23][24].…”
Section: Introductionmentioning
confidence: 99%