Sustainable Carbon Materials From Hydrothermal Processes 2013
DOI: 10.1002/9781118622179.ch3
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Porous Biomass‐Derived Carbons: Activated Carbons

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Cited by 12 publications
(6 citation statements)
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“…As of today, many microporous sorbents are derived from petroleum products or include scarce elements. Consequently, efforts are being made to synthesize sorbents through more sustainable or renewable means. It is established that carbon-rich materials can be synthesized using platform molecules of biorefineries . 5-Hydroxymethylfurfural (HMF) is such a molecule, , which could also be used in fuel additives, as a monomer, and in the synthesis of other chemical derivatives. …”
Section: Introductionmentioning
confidence: 99%
“…As of today, many microporous sorbents are derived from petroleum products or include scarce elements. Consequently, efforts are being made to synthesize sorbents through more sustainable or renewable means. It is established that carbon-rich materials can be synthesized using platform molecules of biorefineries . 5-Hydroxymethylfurfural (HMF) is such a molecule, , which could also be used in fuel additives, as a monomer, and in the synthesis of other chemical derivatives. …”
Section: Introductionmentioning
confidence: 99%
“…The synthesis of carbon nanotubes from plastic by Pol et al is one of the best examples of environmental remediation . Biomasses have been extensively used as precursors for the synthesis of porous and activated carbons via critical steps followed by post activations for application in energy‐related devices . Apart from plant biomass, organically rich human and animal waste also has tremendous potential to generate graphitic carbons .…”
Section: Introductionmentioning
confidence: 99%
“…Impregnation of the hydrochars was performed by soaking the biochars in the solution of phosphoric acid and continuously stirring inside a pressure reactor (Model: 4500, Parr Instrument Company, Moline, IL) at a temperature of 85°C for 24 h. After the impregnation procedure was over, the impregnated samples were oven dried at a temperature of 103°C for 24 h. The oven dried impregnated samples were thereafter activated using a thermogravimetric analyzer at a temperature of 900°C under nitrogen flow to keep the process inert. Among various activation agents, the H 3 PO 4 has been used on lignocellulosic precursors in the activation temperature ranges between 350 and 650°C . In addition, the H 3 PO 4 has also been used for activation of carbohydrate (sucrose, cellulose, and glucose) derived hydrochars.…”
Section: Methodsmentioning
confidence: 99%
“…Therefore, it cleans up existing pores. At temperatures higher than 450°C, it combines with carbon structure to form phosphate and polyphosphate bridges, which dilate carbon structure leaving accessible pore structure . In the current research, 900°C was chosen for activation temperature because the goal was to produce pure carbon matrix with enhanced pore structure but limited or no chemical functionality attached to its surface that would promote redox‐reactions during EDLC testing.…”
Section: Methodsmentioning
confidence: 99%