2019
DOI: 10.1002/slct.201900115
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Biomass‐Derived Lignocellulosic Graphene Composite: Novel Approach for Removal of Oil and Organic Solvent

Abstract: Novel approach to develop a biomass derived lignin‐cellulose based, ultra‐light, hydrophobic graphene supported spongy composite was synthesized to absorb oil and organic solvents from wastewater. Spongy composite was synthesized by a facile and highly efficient one‐pot hydrothermal method from the natural precursor. Lignin‐cellulose functionalized graphene (LCG) sponge was synthesized from graphene oxide (GO) and sugarcane waste powder (SCwP) in presence of natural latex. LCG successfully demonstrated separat… Show more

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Cited by 34 publications
(18 citation statements)
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“…According to XPS analysis, the peak at 284, 400, 532, and 710 eV was showed the presence of C, N, O, and Fe 2p (Figure a XPS survey spectra) respectively. The as prepared GO contained a low C/O ratio of 2.02, which gives two observed peaks at 282.5 and 530.4 eV it indicates that C1s and O1s spectrum respectively (Figure a) . The G@PANI‐Fe 3 O 4 and G@PPy‐Fe 3 O 4 (Figure a) was showed a less C/O ratio of ∼1.92 and ∼1.87 respectively, in contrast to that of GO, which corresponds to the increased oxygen content in the nanocomposite.…”
Section: Resultsmentioning
confidence: 56%
“…According to XPS analysis, the peak at 284, 400, 532, and 710 eV was showed the presence of C, N, O, and Fe 2p (Figure a XPS survey spectra) respectively. The as prepared GO contained a low C/O ratio of 2.02, which gives two observed peaks at 282.5 and 530.4 eV it indicates that C1s and O1s spectrum respectively (Figure a) . The G@PANI‐Fe 3 O 4 and G@PPy‐Fe 3 O 4 (Figure a) was showed a less C/O ratio of ∼1.92 and ∼1.87 respectively, in contrast to that of GO, which corresponds to the increased oxygen content in the nanocomposite.…”
Section: Resultsmentioning
confidence: 56%
“…In the FTIR spectrum of GO, broadband was observed at 3321 cm −1 , indicated O–H bond stretching due to hydroxyl functionality and moisture trapping . The sharp observed peak around 1724 cm −1 , attributable to the presence of carbonyl groups in GO structure . The peak around 1610 cm −1 mainly due to C=C stretching vibration of aromatic conjugated carbons .…”
Section: Resultsmentioning
confidence: 82%
“…[34][35][36][37][38] The sharp observed peak around 1724 cm À 1 , attributable to the presence of carbonyl groups in GO structure. [39][40][41] The peak around 1610 cm À 1 mainly due to C=C stretching vibration of aromatic conjugated carbons. [37,39] The peaks near to 1410 cm À 1 , 1221 cm À 1 and 1048 cm À 1 are because of CÀ H bending, CÀ O-C peak and sp 3 CÀ O stretching.…”
Section: Resultsmentioning
confidence: 99%
“…When temperature was reached at 800°C, the weight loss of about 70 to 75 % was observed due to thermal decay of the carbon skeleton. [46,47] TGA of G@SiO 2 -AR ( Figure 2) and SiO 2 @AR ( Figure S2) shows a minor weight loss was observed at both the stages as compared to the GO. At 600°C, the total weight loss of about 60-65 % was observed for both the samples.…”
Section: Resultsmentioning
confidence: 98%