Department of Chemical & Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695, USA.
Department of Byproducts and Biosystems, School of Chemical Engineering, Aalto University, FI-00076 Aalto, Espoo, Finland; Bioproducts Institute, Departments of Chemical and Biological Engineering, Chemistry and Wood Science, University of British Columbia, Vancouver, BC V6T 1Z3, Canada.
J Colloid Interface Sci. 2021 Apr 15;588:232-241. doi: 10.1016/j.jcis.2020.12.041. Epub 2020 Dec 17.
Nanocellulose and nanochitin are both biobased materials with complementary structures and properties. Both exhibit pH-dependent surface charges which are opposite in sign. Hence, it should be possible to manipulate them to form complexed structures via ionic bond formation at prescribed pH conditions.
Nanocellulose and nanochitin were mixed after exposure to acidic or neutral conditions to influence their ionization state. The heat of interaction during the introduction of nanochitin to nanocellulose was monitored via isothermal titration calorimetry. The strength and gel properties of the resulting structures were characterized via rheological measurement.
The resultant gel properties in the designed hybrid systems were found to depend directly on the charge state of the starting materials, which was dictated by pH adjustment. Different interparticle interactions including ionic attraction, hydrophobic associations, and physical entanglement were identified in the systems and the influence of each was elucidated for different conditions of pH, concentration, and ratio of nanochitin to nanocellulose. Hydrophobic associations between neutralized nanochitin particles were found to contribute strongly to increased elastic modulus values. Ionic complex formation was found to provide enhanced stability under broader pH conditions, while physical entanglement of cellulose nanofibers was a substantial thickening mechanism in all systems.
纳米纤维素和纳米壳聚糖都是具有互补结构和性能的生物基材料。两者都表现出 pH 依赖性表面电荷,其符号相反。因此,应该有可能通过在规定的 pH 条件下形成离子键来操纵它们形成复杂结构。
纳米纤维素和纳米壳聚糖在暴露于酸性或中性条件后混合,以影响它们的电离状态。通过等温热滴定法监测纳米壳聚糖引入纳米纤维素过程中的相互作用热。通过流变测量来表征所得结构的强度和凝胶特性。
在所设计的混合系统中,所得的凝胶特性直接取决于起始材料的电荷状态,这是由 pH 调节决定的。在系统中鉴定了不同的颗粒间相互作用,包括离子吸引、疏水缔合和物理缠结,并阐明了每种相互作用在不同的 pH 值、浓度和纳米壳聚糖与纳米纤维素的比例条件下的影响。发现中和后的纳米壳聚糖颗粒之间的疏水缔合强烈有助于增加弹性模量值。发现离子络合在更宽的 pH 条件下提供增强的稳定性,而纤维素纳米纤维的物理缠结是所有系统中的重要增稠机制。