Constructing a "micro-nano collaboration" network via disk-milling: Value-enhanced utilization of flexible temperature-resistant cellulose insulation films.

Cellulose is a sustainable natural polymer material that has found widespread application in transformers and other power equipment because of its excellent electrical and mechanical performance. However, the utility of cellulose materials has been limited by the challenge of balancing heat resistance with flexibility. On the basis of the preliminary research conducted by the research team, further proposals have been put forward for a method involving disk milling to create a "micro-nanocollaboration" network for the fabrication of flexible, high-temperature-resistant, and ultrafine fiber-based cellulose insulating films. The resulting full-component cellulose films exhibited impressive properties, including high tensile strength (22 MPa), flexibility (92-263 mN), remarkable electrical breakdown strength (39 KV/mm), and volume resistivity that meets the standards for insulation materials (4.92 × 1011 Ω·m). These results demonstrate that the proposed method can produce full-component cellulose insulation films that offer both exceptional flexibility and high-temperature resistance.

Green production of lignocellulose nanofibrils by FeCl3-catalyzed ethanol treatment.

The traditional strategy for isolating cellulose nanomaterials requires various chemicals and a high energy input, while achieving a low product yield owing to lignin removal during pulping and bleaching. Here, we propose a green ethanol pretreatment process with a synergistic effect using ultrasound and FeCl3 to produce lignocellulose nanofibrils (LCNF) with a high yield (over 67 %) from thermomechanical pulp. Notably, a high-aspect-ratio LCNF with uniformly distributed lignin nanoparticles, a high lignin content, and excellent thermostability (Tmax > 330 °C) with a typical cellulose I crystalline structure were successfully obtained. In addition, reduced distillation can easily retrieve the FeCl3 solution and ethanol, reducing reagent waste. In general, FeCl3-catalyzed ethanol pretreatment can serve as a sustainable and environmentally friendly approach for converting sustainable lignocelluloses into high value-added nanomaterials. Moreover, the obtained LCNF can be applied in diverse fields.

Cellulose nanofibrils (CNFs) in uniform diameter: Capturing the impact of carboxyl group on dispersion and Re-dispersion of CNFs suspensions.

The poor dispersibility and re-dispersibility of cellulose nanofibrils (CNFs) in various solvents and polymers have been recognized as the key factors limiting their potential applications. TEMPO oxidation, as the most common surface modification, can greatly improve the dispersion and re-dispersion of CNFs. However, the diameter of TEMPO-oxidized cellulose nanofibers (TOCNFs) has not been regulated in most researches, which was an important factor determining the dispersion and re-dispersion of TOCNFs. Herein, this work explored the effect of carboxyl groups on dispersion and re-dispersion of TOCNFs with uniform diameter in various solvents. Notably, fractal dimension was innovatively introduced to characterize the distribution of TOCNFs diameter. The fractal dimension and statistic diameter of TCONFs with different carboxyl group contents are ~1.56 and ~22 nm, demonstrating that the diameter of TOCNFs has been regulated in the same range. When the carboxyl group content is up to 1.58 mmol/g, the dispersion and re-dispersion of TOCNFs suspension in water and different organic solvents are the most uniform and stable. In a word, this work explores the dispersion and re-dispersion of TOCNFs with the uniform diameter and different carboxyl group contents, which can provide the theoretical guidance for various potential applications of nanofibrils in polymer matrix composites.

Solvent-free preparation of thermoplastic bio-materials from microcrystalline cellulose (MCC) through reactive extrusion.

Cellulose, as a renewable biopolymer, was acknowledged as a promising alternative for petroleum polymer. However, the poor thermoplasticity of cellulose caused a limitation in its full development. Herein, a solvent-free and simple strategy was proposed for the preparation of thermoplastic bio-materials from microcrystalline cellulose (MCC). Kraft lignin (KL) was employed as a plasticizer in this work. It was demonstrated that MCC-based materials with great thermoplasticity and mechanical properties could be successfully prepared by reactive extrusion. The obtained MCC-based material ML8G (with 50 wt% KL adding) possessed great thermostability and thermoplastic properties with an obvious glass transition temperature (Tg) at 106 °C. In addition, the bending strength, flexural modulus and storage modulus of the MCC-based material were improved to 20.44 MPa, 3139.47 MPa and 5.81 GPa respectively. Furthermore, the obtained MCC-based material exhibited good water stability and biodegradability. The comprehensive results confirmed the feasibility of MCC-based materials plasticized with KL through reactive extrusion. Overall, this work was a promising development in the field of bio-plastic utilization of natural products from a green source.

Insights into structure and properties of cellulose nanofibrils (CNFs) prepared by screw extrusion and deep eutectic solvent permeation.

To achieve the balance on economy and ecology, it is indispensable to explore the greener and more inexpensive method for the production of cellulose nanofibrils (CNFs). Herein, a deep eutectic solvent (DES) system based on choline chloride (ChCl) and ethylene glycol (EG) was employed as the swollen solvent, combining with screw extrusion and permeant, to fabricate unmodified CNFs with high yield and thermal stability. The proposed method in this work was simple, convenient, and industrially viable. The hydrous DESs were applied in the process of CNFs preparation and dispersion to reduce the cost and viscosity of DES. To reveal the principle of CNFs preparation, the impact of sulfuric acid and water content of DES system on the chemical, physical, morphological, thermal, and dispersive properties of CNFs was systematically studied. Properties of the dispersed solvents were characterized by solvatochromic parameters and viscosity parameters to evaluate the potential influence on the preparation and dispersion of CNFs. In general, this work would play valuable guidance in realizing the preparation and dispersion of CNFs via a versatile DES solvent system, thus endowing cellulose materials high-value utilization.

Dissolution of Lignocelluloses with a High Lignin Content in a N-Methylmorpholine-N-oxide Monohydrate Solvent System via Simple Glycerol-Swelling and Mechanical Pretreatments.

Lignocelluloses (LCs) with various amounts of lignin (even as high as 18.4%) were successfully dissolved in N-methylmorpholine-N-oxide monohydrate (NMMO/H2O) solution with stirring at 85 °C within 5 h. For the developmental dissolution methods of LCs with a high lignin content in NMMO/H2O solution, the following two pretreatment steps of LCs were necessary: (1) glycerol swelling and (2) mechanical extrusion. The mechanical extrusion pretreatment under glycerol swelling dissociated the fiber bundles of LCs to thinner fibers and, thus, enhanced the accessibility and solubility of the LCs in NMMO/H2O. The crystal structure of the pretreated LCs had no significant transformation during pretreatment, while the diameters of the fiber bundles were reduced from 50-60 to 10-12 µm, as investigated by X-ray diffraction and scanning electron microscopy. After the dissolution-regeneration process of LCs, the fiber bundles of the LCs disappeared and the crystal type of cellulose in the LCs was transformed from cellulose I to cellulose II, which indicated the complete dissolution of LCs.

Closing of the fingers domain generates motor forces in the HIV reverse transcriptase.

Using the force sensor of an atomic force microscope, motor forces of the human immunodeficiency virus-1 reverse transcriptase were measured during active replication of a short DNA transcript. At low load forces the polymerase is mechanically slowed, whereas at high force (approximately 15 piconewton) it stalls. From recordings of estimated polymerase turnover velocity versus load force, an approximate force-velocity curve has been constructed. The shape of the curve suggests that load force strongly inhibits the rate-limiting step of the polymerase turnover cycle and that the combined effect of load on all steps involves an effective motion of about 1.6 nm. Earlier results from pre-steady-state kinetics experiments have identified the rate-limiting step as the closing of the fingers domain to form a tight catalytic complex. Together these findings indicate that the closing of the fingers domain is a major force-generating step for human immunodeficiency virus reverse transcriptase and, by extension, for all DNA polymerase machines.