Characterization of white poplar and eucalyptus after ionic liquid pretreatment as a function of biomass loading using X-ray diffraction and small angle neutron scattering
Abstract:A systematic study was performed to understand interactions among biomass loading during ionic liquid (IL) pretreatment, biomass type and biomass structures. White poplar and eucalyptus samples were pretreated using 1-ethyl-3-methylimidazolium acetate (EmimOAc) at 110°C for 3h at biomass loadings of 5, 10, 15, 20 and 25wt%. All of the samples were chemically characterized and tested for enzymatic hydrolysis. Physical structures including biomass crystallinity and porosity were measured by X-ray diffraction (XR… Show more
“…Surprisingly, it keeps increasing with increasing biomass concentration until 20 wt % . Biomass porosity increases as a result of removal and/or redistribution of biomass components and swelling of biomass samples during pretreatment. , In the previous work, a lower IL-to-biomass ratio during IL pretreatment led to removal of a lesser amount of biomass components and therefore smaller porosity . As shown in the right axis of Figure d, the percentage of recovered solids after pretreatment slightly increases from 80 to 84 wt % with increasing biomass concentrations, consistent with prior work.…”
Section: Resultssupporting
confidence: 87%
“…SANS and USANS can also track changes in structure of biomass samples during the course of enzymatic digestion, thus offering a unique tool to understand biomass pretreatment and enzymatic hydrolysis. 14,15 Relative changes in porosity of white poplar and eucalyptus after ionic liquid pretreatment were analyzed by SANS in a previous work. 15 In this study, changes in porosity of pine samples as a function of ionic liquid (IL) pretreatment conditions were studied using both SANS and nitrogen adsorption measurements, which demonstrated the applicability of SANS to the study of the porosity of biomass samples.…”
Small-angle neutron scattering (SANS) was used to study the porosity of pine samples before and after ionic liquid (IL) pretreatment. Pine samples were pretreated using 1-ethyl-3-methylimidazolium acetate ([C2C1Im][OAc]) at 110 °C for 3 h at biomass concentrations of 5, 10, 15, 20, and 25 wt % and at 130 °C for 3 h at biomass concentrations of 5 and 25 wt %. For the first time, relative changes in porosity of pretreated pine samples derived from SANS were compared with those obtained from the nitrogen adsorption analysis. Biomass crystalline structures were measured by X-ray diffraction (XRD). Both porosity and XRD data suggest that [C2C1Im][OAc] interacted with pine samples more efficiently at higher biomass concentrations during pretreatment. This was attributed to the presence of resin acid in the pine samples.
“…Surprisingly, it keeps increasing with increasing biomass concentration until 20 wt % . Biomass porosity increases as a result of removal and/or redistribution of biomass components and swelling of biomass samples during pretreatment. , In the previous work, a lower IL-to-biomass ratio during IL pretreatment led to removal of a lesser amount of biomass components and therefore smaller porosity . As shown in the right axis of Figure d, the percentage of recovered solids after pretreatment slightly increases from 80 to 84 wt % with increasing biomass concentrations, consistent with prior work.…”
Section: Resultssupporting
confidence: 87%
“…SANS and USANS can also track changes in structure of biomass samples during the course of enzymatic digestion, thus offering a unique tool to understand biomass pretreatment and enzymatic hydrolysis. 14,15 Relative changes in porosity of white poplar and eucalyptus after ionic liquid pretreatment were analyzed by SANS in a previous work. 15 In this study, changes in porosity of pine samples as a function of ionic liquid (IL) pretreatment conditions were studied using both SANS and nitrogen adsorption measurements, which demonstrated the applicability of SANS to the study of the porosity of biomass samples.…”
Small-angle neutron scattering (SANS) was used to study the porosity of pine samples before and after ionic liquid (IL) pretreatment. Pine samples were pretreated using 1-ethyl-3-methylimidazolium acetate ([C2C1Im][OAc]) at 110 °C for 3 h at biomass concentrations of 5, 10, 15, 20, and 25 wt % and at 130 °C for 3 h at biomass concentrations of 5 and 25 wt %. For the first time, relative changes in porosity of pretreated pine samples derived from SANS were compared with those obtained from the nitrogen adsorption analysis. Biomass crystalline structures were measured by X-ray diffraction (XRD). Both porosity and XRD data suggest that [C2C1Im][OAc] interacted with pine samples more efficiently at higher biomass concentrations during pretreatment. This was attributed to the presence of resin acid in the pine samples.
“…During this process, the crystalline form of cellulose is transformed, and the hydrogen bonds between molecules are broken and rearranged, reducing the crystallinity of cellulose and increasing the pores (Yuan et al 2017). Metal ions are often used to promote hydrolysis to pretreat cellulose because the empty orbitals of metal ions can combine with the lone pair of electrons on the β-1,4 glycosidic bond oxygen atom of cellulose (Li et al 2015), thereby activating the carbon-oxygen bond, which is conducive to cellulose hydrolysis.…”
In this paper, tannic acid, a polyphenolic substance rich in plants, is modified by the glutamic acid and cross-linked with formaldehyde to prepare a high acid density tannin-glutamate acid resin-based imitation enzyme solid acid catalyst (T-Glu-R), which is completely different from traditionally carbon-based solid acid synthesized by concentrated sulfuric acid and carbonized matter. The solid acid catalyst was characterized by Fourier transform infrared spectroscopy, scanning electron microscope, thermogravimetry, and X-ray photoelectron spectroscopy. The catalytic activity and cycle performance of T-Glu-R in the cellulose hydrolysis reaction were evaluated. The results show that the acid density of T-Glu-R reached 7.28 mmol/g, which is much higher than that of the highest acid density of carbon-based solid acid. Microcrystalline cellulose was hydrolyzed in distilled water at 180 °C for 2 h, the yield of total reducing sugars reached 72.15%. After four cycles of hydrolysis, the yield was only reduced by 4.32%, showing excellent cycle performance and stability. The study provides a new strategy with the synthesis of solid acid catalyst for hydrolysis of cellulose converted into platform compounds without concentrated sulfuric acid.
“…Concerns over oil prices as well as the harm caused by fossil fuel consumption have accelerated bioeconomy-related research (Mortimer 2019). This includes plants genetically engineered to synthesize valuable compounds (Zhang et al 2015;Eudes et al 2016aEudes et al , 2016b, methods developed to isolate those chemicals or intermediates and a maximum amount of accessible carbon from plant biomass (Neupane et al 2017;Pérez-Pimienta et al 2017;Yuan et al 2017), as well as microorganisms engineered to efficiently convert plant-derived carbon into desirable products (Phelan et al 2015;Goh et al 2018;Sasaki et al 2019; Figure 1).…”
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