Preparation of Dissolving Pulp by Combined Mechanical and Deep Eutectic Solvent Treatment.

Grasses are potential candidate to replace wood as a raw material for pulping and paper making, and several processes have been developed to produce grass pulp. In this study, wheat straw was used as raw material, and the possibility of sequential treatment with a mechanical method and deep eutectic solvent (DES) to prepare high-quality dissolving pulp was explored. Firstly, the wheat straw was mechanically treated, and then the wheat straw was delignified using a choline chloride-lactic acid deep eutectic solvent. The results showed that the optimal treatment conditions of deep eutectic solvent were 110 °C, 6 h, and a solid-liquid ratio (ratio of pulp to DES) of 1:40. The removal rate of lignin was 82.92%, the glucose content of pulp was increased by 11.42%. The DES recovery rate was further calculated, and the results showed that the DES recovery rate was more than 50% with rotary evaporation. The pulp viscosity after bleaching was 472 mL/g, and the α-cellulose accounted for 81.79%. This treatment has advantages in biomass refining, and the total utilization rate of wheat straw reaches 72%. This study confirmed that combined mechanical and deep eutectic solvent treatment can effectively remove lignin from wheat straw to produce high-quality wheat straw dissolving pulp.

High performance bio-supercapacitor electrodes composed of graphitized hemicellulose porous carbon spheres.

A template-free and one-step carbonization process was developed for fabricating graphitic porous carbon spheres (GPCSs) on hemicelluloses as the electrode material for supercapacitors. This method is green, low-energy, and less time consuming compared to the conventional two-step process (pore-forming and graphitizing). It uses K2FeO4, a mild activating agent that fulfills synchronous activation and graphitization. The GPCSs is regular spherical shape, have high nanoporosity, a large specific surface area (1,250 m2 g-1), and have a high graphitization degree. A unique structural advantage includes a rich interconnected conductive network for electron transfer that shortens the ion transport distance of the electrolyte. Remarkably, the GPCSs electrode displays outstanding electrochemical performance including high specific capacitance (262 F g-1 at 1.0 A g-1), rate capability energy (80%, 20 A g-1), and excellent cycling stability (95%, 10,000 cycles). This work represents a powerful methodology to develop sustainable and low-cost energy storage devices from hemicellulose.

Preparation of Salt-Induced Ultra-Stretchable Nanocellulose Composite Hydrogel for Self-Powered Sensors.

Hydrogels have attracted much attraction for promising flexible electronics due to the versatile tunability of the properties. However, there is still a big obstacle to balance between the multi-properties and performance of wearable electronics. Herein, we propose a salt-percolated nanocellulose composite hydrogel which was fabricated via radical polymerization with acrylic acid as polymer networks (NaCl-CNCs-PAA). CNCs were utilized as a reinforcing agent to enhance the mechanical properties of the hydrogel. Moreover, the abundant hydroxyl groups endow the hydrogel with noncovalent interactions, such as hydrogen bonding, and the robustness of the hydrogel was thus improved. NaCl incorporation induced the electrostatic interaction between CNCs and PAA polymer blocks, thus facilitating the improvement of the stretchability of the hydrogel. The as-obtained hydrogel exhibited excellent stretchability, ionic conductivity, mechanical robustness and anti-freezing properties, making it suitable for self-powered sensing applications. A single-mode triboelectric nanogenerator (C-TENG) was fabricated by utilizing the composite hydrogel as electrodes. This C-TENG could effectively convert biomechanical energy to electricity (89.2 V, 1.8 µA, 32.1 nC, and the max power density of 60.8 mW m-2 at 1.5 Hz.) Moreover, the composite hydrogel was applied for strain sensing to detect human motions. The nanocellulose composite hydrogel can achieve the application as a power supply in integrated sensing systems and as a strain sensor for human motion detection.

A multifunctional nanocellulose-based hydrogel for strain sensing and self-powering applications.

Ionic conductive hydrogel with multifunctional properties have shown promising application potential in various fields, including electronic skin, wearable devices and sensors. Herein, a highly stretchable (up to 2800% strain), tough, adhesive ionic conductive hydrogel are prepared using cationic nanocellulose (CCNC) to disperse/stabilize graphitic carbon nitride (g-C3N4), forming CCNC-g-C3N4 complexes and in situ radical polymerization process. The ionic interactions between CNCC and g-C3N4 acted as sacrificial bonds enabled highly stretchability of the hydrogel. The hydrogel showed high sensitivity (gauge factor≈5.6, 0-1.6% strain), enabling the detection of human body motion, speech and exhalation. Furthermore, the hydrogel based self-powered device can charge 2.2 µF capacitor up to 15 V from human motion. This multifunctional hydrogel presents potential applications in self-powered wearable electronics.

Green Synthesis and Characterization of Gold Nanoparticles Using Lignin Nanoparticles.

With the development of nanotechnology, gold nanoparticles (Au NPs) have attracted enormous attention due to their special properties. The green synthesis of Au NPs from lignin would inspire the utilization of lignin and its related functional materials. In this study, a rapid preparation process of Au NPs was investigated by utilizing lignin nanoparticles (LNPs) under room temperature without chemical addition. The LNPs acted as a reducing agent, stabilizing agent, and template for the preparation of LNPs@AuNPs. The obtained LNPs@AuNPs were characterized by UV-Vis spectrum, Transmission Electron Microscope (TEM), and X-ray photoelectron spectroscopy (XPS). The possible mechanism was illustrated by Fourier Transform Infrared Spectroscopy (FT-IR), 31P, XPS, and UV analyses. The abundant hydroxyl groups (24.96 mmol/g) favored the preparation of Au NPs. Au NPs diameters of 10-30 nm were well dispersed in the LNPs. The optimal reaction conditions were a ratio of 10 mg of LNPs to 0.05 mmol HAuCl4, room temperature, and a reaction time of 30 min. The LNPs@AuNPs exhibited excellent stability in the suspension for more than seven days. The reduction process could be related to the disruption of side chains of lignin, hydroxyl group oxidation, and hydroquinones and quinones from the comproportionation reaction. The LNPs@AuNPs would open a door for the design of Au NP/lignin-derived novel functional materials.

Biochars from Lignin-rich Residue of Furfural Manufacturing Process for Heavy Metal Ions Remediation.

The pentose/furfural industrial manufacturing process uses corn cob residue as a raw material, where such a process yields significant amount of lignin-rich residue (LCR) at the end, which is commonly disposed by burning. In this study, the conversion of LCR to biochars (BCs), and their subsequent applications for heavy metal ion removal, were investigated. The BCs were prepared through hydrothermal carbonization and post-activation, using either ZnCl2 or H3PO4 treatment. The as-prepared activated BCs were characterized using N2 adsorption-desorption isotherms, XRD, FT-IR, SEM and TEM, and their performance in removing heavy metal ions (Pb2+, Cu2+, Cd2+) from aqueous solutions was assessed. The ZnCl2-activated BCs (BC-ZnCl2) exhibit a higher adsorption capacity than the H3PO4-activated BCs (BC-H3PO4), mainly due to the differences in their chemical/physical characteristics. The related adsorption kinetics and isotherms were analyzed.

Chitosan-Nanocellulose Composites for Regenerative Medicine Applications.

Regenerative medicine represents an emerging multidisciplinary field that brings together engineering methods and complexity of life sciences into a unified fundamental understanding of structure-property relationship in micro/nano environment to develop the next generation of scaffolds and hydrogels to restore or improve tissue functions. Chitosan has several unique physico-chemical properties that make it a highly desirable polysaccharide for various applications such as, biomedical, food, nutraceutical, agriculture, packaging, coating, etc. However, the utilization of chitosan in regenerative medicine is often limited due to its inadequate mechanical, barrier and thermal properties. Cellulosic nanomaterials (CNs), owing to their exceptional mechanical strength, ease of chemical modification, biocompatibility and favorable interaction with chitosan, represent an attractive candidate for the fabrication of chitosan/ CNs scaffolds and hydrogels. The unique mechanical and biological properties of the chitosan/CNs bio-nanocomposite make them a material of choice for the development of next generation bio-scaffolds and hydrogels for regenerative medicine applications. In this review, we have summarized the preparation method, mechanical properties, morphology, cytotoxicity/ biocompatibility of chitosan/CNs nanocomposites for regenerative medicine applications, which comprises tissue engineering and wound dressing applications.

Comparative Evaluation of Organic Acid Pretreatment of Eucalyptus for Kraft Dissolving Pulp Production.

Pretreatment is an essential process for the extensive utilization of lignocellulose materials. The effect of four common organic acid pretreatments for Kraft dissolving pulp production was comparatively investigated. It was found that under acidic conditions, hemicellulose can be effectively removed and more reducing sugars can be recovered. During acetic acid pretreatment, lignin that was dissolved in acetic acid could form a lignin-related film which would alleviate cellulose hydrolysis, while other organic acids caused severe cellulose degradation. Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and X-ray diffractometry (XRD) were used to characterize the pretreated chips in the process. Lignin droplets were attached to the surface of the treated wood chips according to the SEM results. The FTIR spectrum showed that the lignin peak signal becomes stronger, and the hemicellulose peak signal becomes weaker with acid pretreatment. The XRD spectrum demonstrated that the crystallinity index of the wood chips increased. The acetic acid pretreatment process-assisted Kraft process achieved higher yield (31.66%) and higher α-cellulose (98.28%) than any other organic acid pretreatment. Furthermore, extensive utilization of biomass was evaluated with the acetic acid pretreatment-assisted Kraft process. 43.8% polysaccharide (12.14% reducing sugar and 31.66% dissolving pulp) and 22.24% lignin (0.29% acetic acid lignin and 21.95% sulfate lignin) were recovered during the process. Biomass utilization could reach 66.04%. Acetic acid pretreatment is a promising process for extensive biomass utilization.

A highly efficient thermo responsive palladium nanoparticles incorporated guar gum hydrogel for effective catalytic reactions.

Hydrogel, especially stimuli responsive hydrogel, has attracted enormous attention due to its unique properties for many applications. Herein, Pd NPs@ CNCs was firstly attained by in situgeneration of Pd NPs onto CNCs, and subsequently incorporated into guar gum-based hydrogel, so that a thermo responsive Pd NPs@ CNCs/ guar gum hydrogel catalytic system was obtained. The sol-gel transition was achieved viaa simple heating/cooling cycle: a sol state was obtained above 70 °C, allowing the catalytic reaction; a gel state was attained below 20 °C, allowing the reuse/ recycling of the Pd NPs. Pd NPs were formed by in situ reduction of PdCl2 in the presence of CNCs so that Pd NPs were loaded onto CNCs surfaces. CNCs acted as stabilizers for the Pd NPs. The TEM image showed that the average size of Pd NPs is ˜3 nm. Subsequently, the Pd NPs@ CNCs composites were loaded into the guar gum hydrogel, based on the boron crosslinking chemistry. The hydrogel exhibited rapid sol-gel transition process upon heating (70 °C) and cooling (20 °C) cycles. The Pd NPs loaded sol-gel transition concept was subsequently applied to the Suzuki coupling reactions between aryl bromides and phenyl boronic acids, and a highly efficient catalytic performance (over 85% yield within 2 h) was obtained. The reuse/recycling of the thermo responsive Pd NPs@ CNCs/guar gum hydrogel catalyst system was investigated. This novel Pd NPs loaded thermo-responsive sol-gel transition concept is a promising new catalytic system.

Online Gradient Descent for Kernel-Based Maximum Correntropy Criterion.

In the framework of statistical learning, we study the online gradient descent algorithm generated by the correntropy-induced losses in Reproducing kernel Hilbert spaces (RKHS). As a generalized correlation measurement, correntropy has been widely applied in practice, owing to its prominent merits on robustness. Although the online gradient descent method is an efficient way to deal with the maximum correntropy criterion (MCC) in non-parameter estimation, there has been no consistency in analysis or rigorous error bounds. We provide a theoretical understanding of the online algorithm for MCC, and show that, with a suitable chosen scaling parameter, its convergence rate can be min-max optimal (up to a logarithmic factor) in the regression analysis. Our results show that the scaling parameter plays an essential role in both robustness and consistency.

Semi-Supervised Minimum Error Entropy Principle with Distributed Method.

The minimum error entropy principle (MEE) is an alternative of the classical least squares for its robustness to non-Gaussian noise. This paper studies the gradient descent algorithm for MEE with a semi-supervised approach and distributed method, and shows that using the additional information of unlabeled data can enhance the learning ability of the distributed MEE algorithm. Our result proves that the mean squared error of the distributed gradient descent MEE algorithm can be minimax optimal for regression if the number of local machines increases polynomially as the total datasize.

Ethylene Control Technologies in Extending Postharvest Shelf Life of Climacteric Fruit.

Fresh fruit is important for a healthy diet. However, because of their seasonal production, regional specific cultivation, and perishable nature, it is essential to develop preservation technologies to extend the postharvest shelf life of fresh fruits. Climacteric fruit adopt spoilage because of ethylene, a key hormone associated with the ripening process. Therefore, controlling ethylene activity by following safe and effective approaches is a key to extend the postharvest shelf life of fruit. In this review, ethylene control technologies will be discussed aiming for the need of developing more innovative and effective approaches. The biosynthesis pathway will be given first. Then, the technologies determining the postharvest shelf life of climacteric fruit will be described with special attention to the latest and significant published works in this field. Special attention is given to 1-methylcyclopropene (1-MCP), which is effective in fruit preservation technologies. Finally, the encapsulation technology to improve the stability of 1-MCP will be proposed, using a potential encapsulation agent of 1-MCP, calixarene.

Oil/water interfaces of guar gum-based biopolymer hydrogels and application to their separation.

Oily wastewater treatment has become a significant research subject due to potential environmental related applications, e.g., oil spill remedy process. In this paper, a natural polymer based hydrogel, prepared from guar gum (GG) and metaborate, was coated onto a stainless steel mesh, and the as-prepared hydrogel-coated material was applied for oil/water separation. The strong hydrophilic GG hydrogel imparted excellent underwater oleophobicity and ultra-low oil adhesion. The results proved that the as-prepared GG hydrogel-coated material possessed excellent self-cleaning property and high oil/water separation efficiency.

Transgenic human alpha-hemoglobin stabilizing protein could partially relieve betaIVS-2-654-thalassemia syndrome in model mice.

Beta-thalassemia is an anemia caused by a relative excess of alpha-hemoglobin (alphaHb) due to absent or reduced beta-hemoglobin (betaHb) synthesis. In this study, we explore whether the introduction of alpha-hemoglobin stabilizing protein (AHSP), a chaperone protein for proper folding and stabilization of free alphaHb in red blood cells, thus aiding hemoglobin A (HbA) assembly, could relieve the pathogenic state of red blood cells in beta-thalassemia. For that, a human ahsp vector was constructed to generate transgenic human ahsp mice in a model of beta(IVS-2-654)-thalassemia by microinjecting the vector into fertilized eggs, resulting in the production of double heterozygous mice (h-ahsp(+)/beta(IVS-2-654+)). Real-time quantitative RT-PCR and Western blot analysis confirmed AHSP expression in three h-ahsp(+)/beta(IVS-2-654+) mice. Hematologic determination showed an improvement in the red blood cell indices of these h-ahsp(+)/beta(IVS-2-654+) mice. The red blood cell count and hemoglobin level were elevated to various extents as compared with their diseased siblings. A dramatic reduction in anisocytosis in the peripheral blood of h-ahsp(+)/beta(IVS-2-654+) mice was observed (16.2 +/- 4.6 vs. 30.0 +/- 5.2%). Few erythroid precursors appeared in the liver sinusoids of h-ahsp(+)/beta(IVS-2-654+) mice. Splenomegaly with extramedullary hematopoiesis was also ameliorated. Significantly, serum iron concentration was remarkably reduced as compared with that of h-ahsp(-)/beta(IVS-2-654+) mice (43.2 +/- 14.9 vs. 82.4 +/- 12.9 microM), and iron deposition in the liver was decreased in h-ahsp(+)/beta(IVS-2-654+) mice. All these results suggested amelioration of the anemia phenotype in h-ahsp(+)/beta(IVS-2-654+) mice after introduction of the ahsp gene. We therefore propose that an ahsp transgene could provide an adjuvant method for gene therapy of beta-thalassemia.