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This article elucidates the dissolution of cellulose from different raw materials in NaOH aqueous solution via the combination of synchrotron-radiation-based SAXS/WAXS characterization. The X-ray measurements probed the mesostructure of the cellulose samples during the freeze-thawing cycle allowing tracking the initial swelling of the structure, the kinetics of disintegration of the cellulose crystallites as well as controlling the final state of the cellulose solution, i.e. presence or absence of cellulose aggregates. The individual SAXS and WAXS measurements were fitted and modelled to enable visualisation and tracking of the changes in the structure in relation to temperature during cooling and warming phases. To further increase the understanding of the parameters affecting dissolution different cellulose samples and solution compositions were considered. For this purpose the effect of increasing the concentration of NaOH and adding Zn2+ has been carefully investigated as well as the importance of the cellulose origin. We found consistent development that the dissolution occurs faster at higher concentrations of NaOH and with Zn2+ regardless the origin. Nevertheless, SAXS data show that materials with a larger amount of cellulose I show more apparent swelling in mesoscopic structure than bleached agricultural containing cellulose II. Despite few crystalline residues after the complete cooling-heating cycle shown by WAXS, some cellulose was not completely dissolved as some network structure remained in the samples under the test condition as suggested by SAXS. [ABSTRACT FROM AUTHOR]

The efficient use of softwood in biorefineries requires harsh pretreatment conditions to overcome biomass recalcitrance. Following harsh pretreatments, the hemicellulose is solubilized. Here, we studied the material characteristics of Norway spruce following steam pretreatment at six different severities, relating chemical and structural information to the enzymatic hydrolyzability. Steam pretreatment conditions were defined by two different temperatures (180 °C and 210 °C), with and without the addition of various acids (CH3COOH, H3PO4, H2SO4, SO2). Structural knowledge of the streams is a cornerstone for developing an efficient saccharification process. This study combines advanced structural characterizations to gain fundamental understanding of the influence of severity of pretreatment on spruce. Structural knowledge is a cornerstone in developing an effective saccharification process by modulating pretreatment conditions and enzymes employed. Overall structural properties were assessed by scanning electron microscopy. The effect of stream pretreatment severity on lignin and lignin-carbohydrate bonds was investigated by two-dimensional heteronuclear single quantum correlation nuclear magnetic resonance. Finally, cellulose ultrastructure was studied by applying small/wide-angle X-ray scattering. The structural characteristics of the six pretreated softwood substrates were related to the enzymatic hydrolyzability. With increasing pretreatment severity, surface defibrillation, and lignin depolymeryzation were observed. Further, lignin-carbohydrate complexes signals were detected. Cellulose analysis revealed the rearrangement of microfibrils leading to the formation of larger microfibril aggregates. This microfibril rearrangement likely contributed to the observed increase in enzymatic hydrolysis yields as better enzyme accessibility resulted. [ABSTRACT FROM AUTHOR]

We present a small angle X-ray scattering (SAXS) study of the colloidal structure of regenerated cellulose fibers, air-gap spun from an ionic liquid solution. Based on the data, and a different interpretation of the anisotropic SAXS pattern, we propose a slightly different colloidal structure of the fibers, than what is commonly assumed for regenerated cellulose fibers. Fibers with two different degrees of orientation, as produced by different draw ratios, DR = 2 and 15, respectively, are analyzed. The 2D SAXS pattern is highly anisotropic with striking cross-like pattern, having scattering predominantly perpendicular and parallel to the fiber axis. This cross-like pattern suggest a colloidal structure with oriented crystalline lamellae of ca. 10 nm thickness, embedded within a continuous matrix of amorphous cellulose. The lamellae are oriented with their normal parallel with the fiber axis. Complementary wide angle X-ray diffraction data confirm that the lamellae normal direction corresponds to the cellulose chain direction (c-direction) in the monoclinic cellulose crystal (Cellulose II). [ABSTRACT FROM AUTHOR]

A SAXS/WAXS apparatus with the aid of a specially designed sample cell capable for performing both SAXS and WAXS experiments was used for adsorption studies in nanoporous materials. The applicability of the instrument for structural investigations and its ability for adsorption experiments because of the advanced sample environment were demonstrated by carrying out in situ SAXS measurements during gas physisorption. SAXS profiles of ordered mesoporous silica were measured at selected equilibrium points alongside a dibromomethane (CHBr) adsorption isotherm at 293 K. SBA-15 was the adsorbent of choice because it consists of a regular 2D hexagonal array of cylindrical mesopores that gives rise to Bragg reflections in the small-angle regime. CHBr was selected as a contrast-matching fluid because it has almost the same electron density as silica. We obtained high-quality data comparable to those resulting from experiments performed in synchrotron light sources which produce intense beams of x-rays and support advanced instrumentation for high-resolution diffraction and SAXS studies. The Bragg peaks of the pore lattice are clearly visible for the evacuated sample and at the early stages of the adsorption process. The intensity decrease and the elimination of the Bragg peaks for the saturated sample suggest that an almost perfect contrast matching was achieved. A model has been used for monitoring the fluid condensation and evaporation regime in SBA-15 by taking into account both the Bragg scattering and the diffuse scattering for spatially random pore filling. The results show the absence of spatial correlations between filled pores suggesting random pore filling. [ABSTRACT FROM AUTHOR]