Laura C. Bradley

Selective Detection of Crystalline Cellulose in Plant Cell Walls with Sum-Frequency-Generation (SFG) Vibration Spectroscopy

The selective detection of crystalline cellulose in biomass was demonstrated with sum-frequency-generation (SFG) vibration spectroscopy. SFG is a second-order nonlinear optical response from a system where the optical centrosymmetry is broken. In secondary plant cell walls that contain mostly cellulose, hemicellulose, and lignin with varying concentrations, only certain vibration modes in the crystalline cellulose structure can meet the noninversion symmetry requirements. Thus, SFG can be used to detect and analyze crystalline cellulose selectively in lignocellulosic biomass without extraction of noncellulosic species from biomass or deconvolution of amorphous spectra. The selective detection of crystalline cellulose in lignocellulosic biomass is not readily achievable with other techniques such as XRD, solid-state NMR, IR, and Raman analyses. Therefore, the SFG analysis presents a unique opportunity to reveal the cellulose crystalline structure in lignocellulosic biomass.

Quantification of crystalline cellulose in lignocellulosic biomass using sum frequency generation (SFG) vibration spectroscopy and comparison with other analytical methods

The non-centrosymmetry requirement of sum frequency generation (SFG) vibration spectroscopy allows the detection and quantification of crystalline cellulose in lignocellulose biomass without spectral interferences from hemicelluloses and lignin. This paper shows a correlation between the amount of crystalline cellulose in biomass and the SFG signal intensity. Model biomass samples were prepared by mixing commercially available cellulose, xylan, and lignin to defined concentrations. The SFG signal intensity was found sensitive to a wide range of crystallinity, but varied non-linearly with the mass fraction of cellulose in the samples. This might be due to the matrix effects such as light scattering and absorption by xylan and lignin, as well as the non-linear density dependence of the SFG process itself. Comparison with other techniques such as XRD, FT-Raman, FT-IR and NMR demonstrate that SFG can be a complementary and sensitive tool to assess crystalline cellulose in biomass.

Clickable Janus Particles

Janus particles are colloidal analogues of molecular amphiphiles that can self-assemble to form diverse suprastructures, exhibit motility under appropriate catalytic reactions, and strongly adsorb to fluid-fluid interfaces to stabilize multiphasic fluid mixtures. The chemistry of Janus particles is the fundamental parameter that controls their behavior and utility as colloid surfactants in bulk solution and at fluid interfaces. To enable their widespread utilization, scalable methods that allow for the synthesis of Janus particles with diverse chemical compositions and shapes are highly desirable. Here, we develop clickable Janus particles that can be modified through thiol-yne click reactions with commercially available thiols. Janus particles are modified to be amphiphilic by introducing either carboxyl, hydroxyl, or amine moieties. We also demonstrate that regulating the extent of the modification can be used to control the particle morphology, and thus the type of emulsion stabilized, as well as to fabricate composite Janus particles through sequential click reactions. Modifying Janus particles through thiol-yne click chemistry provides a fast-reacting, scalable synthesis method for the fabrication of diverse Janus particles.

Hydrophobic but hygroscopic polymer films--identifying interfacial species and understanding water ingress behavior.

The hydrophobic but hygroscopic nature of polydimethylsiloxane (PDMS) with quaternary ammonium cationic side chains adsorbed on a SiO(2) surface was investigated with sum frequency generation vibration spectroscopy (SFG) and attenuated total reflectance infrared spectroscopy (ATR-IR). PDMS with cationic side chains, named cationic polymer lubricant (CPL), forms a self-healing boundary lubrication film on SiO(2). It is interesting that CPL films are externally hydrophobic but internally hydrophilic. The comparison of SFG and ATR-IR data revealed that the methyl groups of the PDMS backbone are exposed at the film/air interface and the cationic side groups and counterions are embedded within the film. The hydrophobicity must originate from the surface CH(3) groups, while the ionic groups inside the film must be responsible for water uptake. The surface hydrophobicity can alleviate the capillary adhesion while the hygroscopic property enhances the mobility and self-healing capability of the CPL boundary lubrication film.

Rough Adhesive Hydrogels (RAd gels) for Underwater Adhesion

In this work, underwater adhesion is achieved between biocompatible hydrogels and a suite of substrates. Surface roughness, which is typically detrimental for adhesion in air, is shown to be beneficial for underwater adhesion. Contact between the hydrogels with macroscopically flat substrates, and the resulting nonspecific chemical interaction, is facilitated by surface roughness, which enables drainage of the lubricating fluid layer. Hydrogel composition plays an important role in tuning the gel elasticity and interaction with the substrate. Hydrogels that are adhesive on two sides are synthesized for potential use as versatile adhesives in various applications.