arXiv subjects

Niki Baccile

Publications and source records attributed to Niki Baccile.

22 records · Page 2Linked to original sources

arXiv2020

Unveiling the Interstitial Pressure Between Growing Ice Crystals During Ice-Templating Using a Lipid Lamellar Probe

What is pressure generated by ice crystals during ice-templating? This work addresses this crucial question by estimating the pressure exerted by oriented ice columns on a supramolecular probe composed of a lipid lamellar hydrogel during directional freezing. This process, also known as freeze-casting, has emerged as a unique processing technique for a broad class of organic, inorganic, soft and biological materials. Nonetheless, the pressure exerted during and after crystallization between two ice columns is not known, despite its importance with respect to the fragility of the frozen material, especially for biological samples. By using the lamellar period of a glycolipid lamellar hydrogel as a common probe, we couple data obtained from ice-templated-resolved in situ synchrotron Small Angle X-ray Scattering (SAXS) with data obtained from controlled adiabatic dessication experiments. We estimate the pressure to vary between 1 $\pm$ 10% kbar at-15{\textdegree}C and 3.5 $\pm$ 20% kbar at-60{\textdegree}C.

cond-mat.soft↗

arXiv2020

Single-Molecule Lamellar Hydrogels from Bolaform Microbial Glucolipids

Lipid lamellar hydrogels are rare soft fluids composed of a phospholipid lamellar phase instead of fibrillar networks. The mechanical properties of these materials are controlled by defects, induced by local accumulation of a polymer or surfactant in a classical lipid bilayer. Herein we report a new class of lipid lamellar hydrogels composed of one single bolaform glycosylated lipid obtained by fermentation. The lipid is self-organized into flat interdigitated membranes, stabilized by electrostatic repulsive forces and stacked in micrometer-sized lamellar domains. The defects in the membranes and the interconnection of the lamellar domains are responsible, from the nano- to the micrometer scales, for the elastic properties of the hydrogels. The lamellar structure is probed by combining small angle x-ray and neutron scattering (SAXS, SANS), the defect-rich lamellar domains are visualized by polarized light microscopy while the elastic properties are studied by oscillatory rheology. The latter show that both storage G' and loss G'' moduli scale as a weak power-law of the frequency, that can be fitted with fractional rheology models. The hydrogels possess rheo-thinning properties with second-scale recovery. We also show that ionic strength is not only necessary, as one could expect, to control the interactions in the lamellar phase but, most importantly, it directly controls the elastic properties of the lamellar gels.

cond-mat.soft↗

arXiv2020

Primary and Secondary Hydration Forces between Interdigitated Membranes Composed of Bolaform Microbial Glucolipids

To better understand lipid membranes in living organisms, the study of intermolecular forces using the osmotic pressure technique applied to model lipid membranes has constituted the ground knowledge in the field of biophysics since four decades. However, the study of intermolecular forces in lipid systems other than phospholipids, like glycolipids, has gained a certain interest only recently. Even in this case, the work generally focuses on the study of membrane glycolipids, but little is known on new forms of non-membrane functional compounds, like microbial bolaform glycolipids. This works explores, through the osmotic stress method involving an adiabatic humidity chamber coupled to neutron diffraction, the short-range (< 2 nm) intermolecular forces of membranes entirely composed of interdigitated glucolipids. Experiments are performed at pH 6, when the glucolipid is partially negatively charged and for which we explore the effect of low (16 mM) and high (100 mM) ionic strength. We find that this system is characterized by primary and secondary hydration regimes, respectively insensitive and sensitive to ionic strength and with typical decay lengths of 0.37 +- 0.12 nm and 1.97 +- 0.78 nm.

cond-mat.soft↗

arXiv2019

Soft lamellar solid foams from ice-templating of self-assembled lipid hydrogels: organization drives the mechanical properties

Ice-templating, also referred to as freeze-casting, is a process exploiting unidirectional crystallization of ice to structure macroporous materials from colloidal solutions. Commonly applied to inorganic and polymeric materials, we employ it here to cast soft self-assembled matter into spongy solid foams. Use of ice-templating to cast soft matter is generally confined to polymers. In the case of polymeric hydrogels, cross-linking ensures a good stability towards the harsh conditions (fast cooling at temperatures as low as-80{\textdegree}C) employed during ice-templating. However, freeze-casting of soft systems held together by weak interactions, like in physical gels, has not been explored, because the nonequilibrium conditions could easily disrupt the nano and macroscale organization of self-assembled matter, resulting in a cruel loss of mechanical properties. Whether this is a general assumption or a more specific relationship exists between the structure of the physical gel and the properties of the macroporous solid after ice-templating is the question addressed in this work. We compare two self-assembled lipid hydrogels, of analogous chemical composition and comparable elastic properties under ambient conditions, but different structure: isotropic entangled self-assembled fibers against heterogeneous lipid lamellar phase. Our results show that both materials possess the same phase (fibrillar and lamellar) before 2 and after freeze-casting but the mechanical properties are absolutely at the opposite: the fibrillar hydrogel provides a brittle, highly anisotropic, macroporous fibrous solid while the lamellar hydrogel provides soft, spongy, solid foam with isotropic Young moduli of several kPa, in the same order of magnitude as some soft living tissues.

cond-mat.soft↗