21 research outputs found

    Diffusion and Saponification Inside Porous Cellulose Triacetate Fibers

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    Honeycomb Films of Cellulose Azide: Molecular Structure and Formation of Porous Films

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    Development of value-added micropatterned porous materials from naturally abundant polymers, such as cellulose, are of growing interest. In this paper, regioselectively modified amphiphilic cellulose azide, 3-<i>O</i>-azidopropoxypoly­(ethylene glycol)-2,6-di-<i>O</i>-thexyldimethylsilyl cellulose, with different degrees of substitution (DS) and degrees of polymerization (DP) of the poly­(ethylene glycol) (PEG) side chain, was synthesized and employed in the formation of honeycomb-patterned films. With the variation of the DP and/or DS, the amphiphilicity of the polymer and the pore size of the formed films changed accordingly. It was found that amphiphilicity of the cellulose azide played a significant role in the formation of honeycomb films. Balanced amphiphilicity was of particular importance in the formation of uniform honeycomb films. Via the Cu<sup>I</sup>-catalyzed alkyne–azide [2 + 3] cycloaddition reaction, fluorescent avidin and quantum dots were attached to the films. By means of confocal microscopy, it was confirmed that the functional azido group was preferentially allocated inside the pores. This provides a platform for the development of advanced honeycomb materials with site-specific functionalities, such as biosensors

    Preparation and Characterization of Kraft Lignin-Based Moisture-Responsive Films with Reversible Shape-Change Capability

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    Preparation of moisture-responsive Kraft lignin-based materials by electrospinning blends of Kraft lignin fractions with different physical properties is presented. The differences in thermal mobility between lignin fractions are shown to influence the degree of interfiber fusion occurring during oxidative thermostabilization of electrospun nonwoven fabrics, resulting in different material morphologies including submicrometer fibers, bonded nonwovens, porous films, and smooth films. The relative amount of different lignin fractions and degree of fiber flow and fiber fusion is shown to influence the tendency for the electrospun materials to be transformed into moisture-responsive materials capable of reversible changes in shape. Material characterization by scanning electron microscopy and atomic force microscopy as well characterization of the chemical and physical properties of Kraft lignin fractions by dynamic rheology, <sup>1</sup>H and <sup>13</sup>C NMR, and gel permeation chromatography combined with multiangle laser light scattering are presented. A proposed mechanism underlying moisture-responsiveness, shape change, and shape recovery is discussed based on the differences in chemical structure and physical properties of Kraft lignin fractions

    Design of Functionalized Cellulosic Honeycomb Films: Site-Specific Biomolecule Modification via “Click Chemistry”

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    Value-added materials from naturally abundant polymers such as cellulose are of significant importance. In particular, cellulosic open-framework structures with controlled chemical functionality of the internal surface have great potential in many biosensor applications. Although various cellulose derivatives can form porous honeycomb structured materials, solubility issues and problems with film formation exist. To address this, we have generated robust cellulosic open-framework structures that can be post-functionalized through site-specific modification. Regioselectively modified amphiphilic cellulose azides, 3-<i>O</i>-azidopropoxypoly­(ethylene glycol)-2,6-di-<i>O</i>-thexyldimethylsilyl cellulosics, were synthesized, and honeycomb-patterned films were readily produced by the simple breath figures method. Changing the degree of polymerization (DP) of the pendent ethylene glycol (EG<sub>DP</sub>) groups from 22 to 4 increased the corresponding honeycomb film pore diameters from ∼1.2 to ∼2.6 μm, enabling the potential tuning of pore size. Moreover, these novel azido-functionalized honeycomb films were easily functionalized using Cu­(I)-catalyzed alkyne–azide [2 + 3] cycloaddition reaction; biotin was “clicked” onto the azide functionalized cellulosic honeycomb films without any effect to the film structure. These results indicate this system may serve as a platform for the design and development of biosensors
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