2019
DOI: 10.1007/s12649-019-00627-8
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Optimizing the Acid Hydrolysis Process for the Isolation of Microcrystalline Cellulose from Oil Palm Empty Fruit Bunches Using Response Surface Methods

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Cited by 8 publications
(4 citation statements)
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“…1908 Thermal degradation was seen at a lower temperature than the cellulose sample throughout a wider temperature range, indicating a reduced thermal stability because of a higher number of free ends in the chain, a reduction in molecular weight, and breakdown of cellulose's amorphous domains (Mandal and Chakrabarty 2011). This result was similar with previous studies (Haafiz et al 2013;Hassan et al 2019). PEER-REVIEWED ARTICLE bioresources.com Norazli et al (2023).…”
Section: Thermal Propertiessupporting
confidence: 83%
See 1 more Smart Citation
“…1908 Thermal degradation was seen at a lower temperature than the cellulose sample throughout a wider temperature range, indicating a reduced thermal stability because of a higher number of free ends in the chain, a reduction in molecular weight, and breakdown of cellulose's amorphous domains (Mandal and Chakrabarty 2011). This result was similar with previous studies (Haafiz et al 2013;Hassan et al 2019). PEER-REVIEWED ARTICLE bioresources.com Norazli et al (2023).…”
Section: Thermal Propertiessupporting
confidence: 83%
“…The acid hydrolysis treatment was conducted to obtain MCC according to the optimized method describe by Hassan et al (2019). 10 g oven dried weight of OPEFB cellulose sample was added with 2.5 N hydrochloric acid with the ratio of 1:20 (OPEFB cellulose to dilute acid) and heated using silicon oil at temperature 106 C for 20 min.…”
Section: Production Of Opefb MCCmentioning
confidence: 99%
“…The absorption peaks of samples after pretreatment weakened compared with raw JAS, indicating that components of carbon chains were destroyed by pretreatment. The absorption at 1,700-1,740 cm -1 belonged to the non-conjugated carbonyl group which was probably originated from acetyl or uronic-ester of thexylan , Hassan et al 2020) and its intensity decreased after pretreatment, indicating the acetyl or uronic-ester groups were partly removed during the pretreatment. The absorption of conjugated carbonyl groups at 1,643 cm -1 primarily correspond to phenolic acids that possess an unsaturated double bond and a carbonyl group (Li et al 2016).…”
Section: Fourier Transform Infrared Analysesmentioning
confidence: 99%
“…Decreasing peak intensity at 1,643 cm -1 indicated that the chemical bond was broken during treatment. Absorption at 1,510 cm -1 corresponds to C=C aromatic skeletal vibration (Hassan et al 2020) and a corresponding characteristic peak at 1,506 cm -1 weakened, indicating that the lignin structure was destroyed and lignin content decreased. A peak at 896 cm -1 was associated with the characteristic absorption of β-glycosidic bonds between glucose units (Oh et al 2005) and its intensity increased after treatment, suggesting increased cellulosic content in the pretreated samples.…”
Section: Fourier Transform Infrared Analysesmentioning
confidence: 99%