Particle morphology characterization and manipulation in biomass slurries and the effect on rheological properties and enzymatic conversion.

An improved understanding of how particle size distribution relates to enzymatic hydrolysis performance and rheological properties could enable enhanced biochemical conversion of lignocellulosic feedstocks. Particle size distribution can change as a result of either physical or chemical manipulation of a biomass sample. In this study, we employed image processing techniques to measure slurry particle size distribution and validated the results by showing that they are comparable to those from laser diffraction and sieving.

Laboratory-scale method for enzymatic saccharification of lignocellulosic biomass at high-solids loadings.

Background: Screening new lignocellulosic biomass pretreatments and advanced enzyme systems at process relevant conditions is a key factor in the development of economically viable lignocellulosic ethanol. Shake flasks, the reaction vessel commonly used for screening enzymatic saccharifications of cellulosic biomass, do not provide adequate mixing at high-solids concentrations when shaking is not supplemented with hand mixing.

Results: We identified roller bottle reactors (RBRs) as laboratory-scale reaction vessels that can provide adequate mixing for enzymatic saccharifications at high-solids biomass loadings without any additional hand mixing.

Particle concentration and yield stress of biomass slurries during enzymatic hydrolysis at high-solids loadings.

Effective and efficient breakdown of lignocellulosic biomass remains a primary barrier for its use as a feedstock for renewable transportation fuels. A more detailed understanding of the material properties of biomass slurries during conversion is needed to design cost-effective conversion processes. A series of enzymatic saccharification experiments were performed with dilute acid pretreated corn stover at initial insoluble solids loadings of 20% by mass, during which the concentration of particulate solids and the rheological property yield stress (tau(y)) of the slurries were measured.

Structural origins of dynamical heterogeneity in colloidal gels.

We show by resolving single-particle dynamics as a function of contact number that dynamical heterogeneity in depletion colloidal gels must have more than one structural origin. Although the magnitude of dynamical heterogeneity of weak gels with cluster structure and strong gels with string structure is similar, the dependence of particle localization on contact number differs significantly in each. The observed transition between contact number dependent and independent dynamics for the weak and strong gels is abrupt.

Viscous solvent colloidal system for direct visualization of suspension structure, dynamics and rheology.

We introduce a model colloid system comprised of particles dispersed in a viscous solvent that can be applied to 3D direct visualization studies of suspension structure, dynamics and rheology. The colloids are poly(methyl methacrylate) (PMMA) spheres sterically stabilized by a copolymer of poly(diphenyl-dimethyl) (DPDM) siloxane that matches the refractive index of PMMA. The monodisperse particles, synthesized with mean diameter varying from 0.

Structure and dynamics of colloidal depletion gels: coincidence of transitions and heterogeneity.

Transitions in structural heterogeneity of colloidal depletion gels formed through short-range attractive interactions are correlated with their dynamical arrest. The system is a density and refractive index matched suspension of 0.20 volume fraction poly(methyl methacyrlate) colloids with the nonadsorbing depletant polystyrene added at a size ratio of depletant to colloid of 0.