Sodium alginate/sodium lignosulfonate hydrogel based on inert Ca2+ activation for water conservation and growth promotion.

Soil degradation has become a major global problem owing to the rapid development of agriculture. The problems of soil drought and decreased soil fertility caused by soil degradation severely affect the development of the agricultural and forestry industries. In this study, we designed sodium alginate (SA)/sodium lignosulfonate (SLS) hydrogel based on the activation and crosslinking of inert Ca2+. CaCO3 and SA were mixed, and then, inert Ca2+ was activated to prepare a gel with a stable structure and a uniform interior and exterior. The crosslinking activated by inert Ca2+ enhanced the stability of the hydrogel, and the optimal swelling rate of the hydrogel reached 28.91 g/g, thereby effectively improving the water-holding capacity of the soil (77.6-108.83 g/kg). SLS was degraded into humic acid (HA) and gradually released, demonstrating a positive growth-promoting effect in plant growth experiments. The SA/SLS hydrogel can be used for soil water retention and mitigation to significantly decrease the water loss rate of soil. This study will assist in addressing soil drought and fertility loss.

RGO-Induced Flower-like Ni-MOF In Situ Self-Assembled Electrodes for High-Performance Hybrid Supercapacitors.

Currently, the primary bottlenecks that hinder the widespread application of supercapacitors are low energy density and narrow potential windows. Herein, the hybrid supercapacitor with high energy density and wide potential window is constructed via an in situ self-assembly method employing RGO-induced flower-like MOF(Ni). Benefiting from the synergistic effect between RGO and MOF(Ni), the interfacial interactions are effectively improved, and the contact area with the electrolyte is enhanced, which increases the ion transfer kinetics and overall electrochemical performance. The MOF(Ni)@RGO electrode exhibits a specific capacitance of 1267.73 F g-1 at a current density of 1 A g-1. Crucially, the assembled MOF(Ni)@RGO//BC with a broad potential window and good stability employing a MOF(Ni)@RGO anode and biomass carbon cathode, combined with a 2 M PVA-KOH gel-electrolyte, achieves a maximum energy density of 70.16 Wh kg-1 at a power density of 2200.09 W kg-1, outperforming most reported supercapacitors. This hybrid supercapacitor exhibits excellent stability and high energy density, providing a novel strategy for further large-scale applications.

Amoxicillin-laded sodium alginate/cellulose nanocrystals/polyvinyl alcohol composite nanonetwork sponges with enhanced wound healing and antibacterial performance.

Wound healing is a complex process and reuires a long repair process. Poor healing effect is normally a challenge for wound healing. Designing sponge dressings with drug-assisted therapy, good breathability, and multiple functional structures effectively promotes wound healing. In this work, a flexible amoxicillin-laded (AMX) sodium alginate (SA)/cellulose nanocrystals (CNCs)/ polyvinyl alcoho (PVA) (SA/CNCs/PVA-AMX, SCP-AMX) wound dressing was designed and built with an excellent porous structure, suitable porosity, and anti-bacterial properties for promoting wound tissue reparation. The porous structure of the wound dressing was fabricated by freeze-thawing cyclic and freeze-dried molding process. This wound dressing exhibited a 3D porous structure for soft-tissue-engineering application, including high porosity (84.2%), swelling ratio (1513%), tensile strength (1.79 MPA), and flexibility. With the inhibition zones of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) being 1.96 and4.58 cm, respectively, this wound dressing demonstrated good antibacterial activity against E. coli and S. aureus. More importantly, wound healing assay in vivo indicates that SCP-AMX could inhibit wound infection, promote collagen deposition, reduce inflammation, and accelerate granulation tissue and wound healing. Thus, the reported wounding dressings present excellent biocompatibility, high antibacterial activities, and excellent biosafety with great potential in wound healing applications.

Constructing 3D hierarchical TiO2 microspheres with enhanced mass diffusion for efficient glucose photoreforming under modulated reaction conditions.

Three-dimensional (3D) TiO2 hierarchical microspheres (THMs) were successfully prepared via a facial template-free hydrothermal approach. The possible growth mechanism of THM was also investigated by TiCl4 concentration-, time-, and temperature-dependent experiments. The results indicate that the formation of an urchin-like hierarchical structure may follow a "nucleation-dissolution and recrystallization-assembly" process. THM was employed for photoreforming under various catalyst and glucose concentrations, solvent compositions, and pH values. The H2 production rate, glucose conversion, arabinose and formic acid selectivity reached 9.44 mmol gcat.-1h-1, 86.35%, 11.32%, and 46.87%, respectively, under the modulated condition with Pt as cocatalyst; this is attributed to the enhanced mass diffusion caused by the 3D hierarchical morphology as well as the interaction between unsaturated Ti atoms (or oxygen vacancies) in THM and the hydroxyl oxygen atoms on glucose. In addition, the enhanced light absorption induced by defects also exerts a positive effect. In this work, we present an emerging sustainable strategy for the coproduction of H2 and value-added chemicals from biomass-based glucose with economic photocatalysts under mild conditions.

Effective enhancement of electron migration and photocatalytic performance of nitrogen-rich carbon nitride by constructing fungal carbon dot/molybdenum disulfide cocatalytic system.

To find a cocatalyst that can replace noble metals, fungal carbon dot (CD) modified molybdenum disulfide (MoS2) cocatalyst system was designed. The composites were prepared by hydrothermal and calcination methods with different ratios of CDs, MoS2 and nitrogen-rich carbon nitride (p-C3N5). p-C3N5 has excellent electronic properties, and MoS2 modified by CDs (D-MoS2) can significantly enhance the photocatalytic performance of p-C3N5 by improving the photogenerated electron migration efficiency. The experiments showed that the developed CDs/MoS2/C3N5 composites exhibited excellent performance in both photocatalytic hydrogen (H2) evolution and methylene blue (MB) degradation, with CMSCN5 (D-MoS2 with 5% mass fraction) showing the best photocatalytic activity. The corresponding H2 evolution rate of CMSCN5 was 444 µmol g-1h-1 and 1.45 times higher than that of unmodified p-C3N5, by 120 min, the removal rate of MB was up to 93.51%. The 5 cycle tests showed that CMSCN5 had great stability. The high charge mobility and high density of H2 evolution active sites of MoS2 nanosheets, together with the electron storage and transfer properties of CDs can obviously improve electron migration and reduce the photogenerated carrier recombination on the p-C3N5 surface. The design and preparation of such composites offer broad prospects for the development of photocatalytic systems with noble metal-free cocatalysts.

Biomass-derived carbon dots regulating nickel cobalt layered double hydroxide from 2D nanosheets to 3D flower-like spheres as electrodes for enhanced asymmetric supercapacitors.

Layered double hydroxides (LDHs) often require the use of carbon materials to improve their stability, conductivity, and specific surface area to accommodate new directions in the development of high-performance energy storage materials. Herein, 2D nickel cobalt layered double hydroxide (NCLDH) nanosheets are regulated to form 3D flower-like spheres by fungus bran-derived carbon dots (CDs) via an in situ growth method. The prepared sample (CDs/NCLDH) shows abundant accessible active sites and favorable electrical conductivity, which is aided by strong interactions between CDs and NCLDH. The optimized CDs/NCLDH exhibits significantly enhanced electrochemical performances, including ultrahigh specific capacitance (2100F g-1 at 1 A g-1) and a great rate capability, which are two times higher than those of the NCLDH electrode. Additionally, the asymmetric supercapacitor device assembled with the CDs/NCLDH positive electrode and the fungus bran-derived activated carbon (FBC) negative electrode achieves a superior energy density of 52.5 Wh kg-1 at an ultrahigh powder density of 750 W kg-1. With their simple synthesis method and excellent electrochemical performance, the role of the CDs provides new insights for the development of LDHs with improved performance.

Selective Isolation Methods for Cellulose and Chitin Nanocrystals.

This Minireview focuses on the selective isolation methods for the preparation of cellulose nanocrystals (CNCs) and chitin nanocrystals (ChNCs). Various selective preparation strategies with specific preparation conditions and reaction mechanisms are summarized. In particular, these selective reaction routes include controlled acid hydrolysis and selective oxidations at specific positions of cellulose or chitin fibers as well as particular reaction sites of the repeating monosaccharide building blocks of their main chains. These lead to selective cleavage of the ordered and non-ordered regions of cellulose and chitin and result in efficient production of CNCs and ChNCs.

Constructing CeO2/nitrogen-doped carbon quantum dot/g-C3N4 heterojunction photocatalysts for highly efficient visible light photocatalysis.

Ternary CeO2/nitrogen-doped carbon quantum dot (NCQD)/graphitic carbon nitride (g-C3N4) heterojunction nanocomposites were prepared by a high-temperature calcination and hydrothermal method and tested for degrading tetracycline (TC) and generating H2. Compared with CeO2 and g-C3N4, the Z-scheme CeO2/NCQDs/g-C3N4 (CSNx, where x represents the amount of CeO2 in wt%) nanoparticles showed a higher TC photodegradation capacity and H2 evolution ability owing to enhanced efficient charge separation and photocatalytic stability. CSN5 showed the best photodegradation activity for TC degradation (100 mL, 20 mg L-1; 100% degradation in 60 min; λ≥ 420 nm) and the highest H2 evolution rate of 1275.42 µmol h-1 g-1 was approximately 3.73- and 32.25-times higher than those of pristine g-C3N4 (341.85 µmol h-1 g-1) and pure CeO2 (39.55 µmol h-1 g-1), respectively. Superoxide (˙O2-) and hydroxyl (˙OH) radicals were also confirmed to be formed on the sample surface for TC photocatalytic degradation. As an electronic medium, NCQDs transferred electrons between the g-C3N4 and CeO2 interface to promote the electron-hole separation. This work affords a helpful perspective for synthesizing efficient charge separation and environmentally friendly photocatalysts by controlling the surface heterostructure.

Novel low-cost carboxymethyl cellulose microspheres with excellent fertilizer absorbency and release behavior for saline-alkali soil.

Saline-alkali soil and fertilizer loss severely restrict agriculture on the Songnen Plain in China. To resolve this problem, carboxymethyl cellulose immobilized slow-release fertilizer microspheres (CFM) with homogeneity pore structure, high porosity, biodegradable biological macromolecules and excellent fertilizer absorbency were synthesized by the combination of inverse emulsion polymerization and microfluidic method. By optimizing the synthesis conditions, the water absorption of CFM reached 8725 g g-1 in deionized water. The absorbency behaviors of CFM were highly sensitive to pH, ionic strength, and ionic species. In 5 g L-1 urea solution, the adsorption capacity of CFM was 3342.84 g g-1. The CFM showed excellent urea retention at 80 °C for 5 h and sustained release performance in soil. Besides, degradation rate of CFM was closed to 98.2% in Aspergillus niger at the third day. CFM had the advantages of high pH sensitivity, salt resistance, and good fertilizer absorbency and retention. Therefore, it will be prospecting fertilizer sustained release agent in agriculture.

Bio-templated 3D porous graphitic carbon nitride hybrid aerogel with enhanced charge carrier separation for efficient removal of hazardous organic pollutants.

Graphitic carbon nitride (g-C3N4) hybrid aerogels (GHAs) with different proportions of g-C3N4 were prepared using g-C3N4, carboxymethyl cellulose, and ß-cyclodextrin. GHAs have demonstrated high porosity, large specific surface area, rich three-dimensional network structure. GHAs demonstrated an excellent synergistic effect on the photocatalytic and adsorptive properties. Especially, GHA1 (the ratio of g-C3N4 and aerogel component was 1:1) exhibited a good synergy in photodegradation and adsorption, with a Rhodamine B (Rh B) removal up to 97.99% in 90 min. In five cycling experiments, the GHA1 showed a good long-term stability. The aerogels can be easily isolated and maintains its excellent photocatalytic properties. Compared to pure g-C3N4, GHA1 has a stronger photocurrent, which is due to the transmission of light to the surface of the catalyst, promoted photo-generated electron-hole pairs, and inhibited recombination of electros and holes. Finally, mechanistic studies reveal that the superoxide radicals (O2-) are the main active groups in the photocatalytic degradation process. This work provides a useful perspective in design and fabrication of hybrid aerogel composites with an enhanced photocatalytic activity.

Biomass-derived nitrogen-doped carbon quantum dots: highly selective fluorescent probe for detecting Fe3+ ions and tetracyclines.

Nitrogen-doped carbon quantum dots (N-CQDs) were successfully synthesized using rice residue and glycine as carbon and nitrogen sources by one-step hydrothermal method. High quantum yield (23.48%) originated from the effective combination of nitrogen with various functional groups (CO, NH, CN, COOH and COC). The N-CQDs showed a fluorescence with the wavelength varied from 420 to 500 nm and the maximum emission wavelength being at 440 nm. N-CQDs have been importantly applied as probe to detect Fe3+ and tetracycline (TCs) antibiotics with remarkable performance. Using the linear relationship between fluorescence intensity and Fe3+ concentration, the N-CQDs could be employed as a simple, efficient sensor for ultrasensitive Fe3+ detection ranging from 3.32 to 32.26 µM, with a limit of detection (LOD) of 0.7462 µM. The N-CQDs showed the applicability to detect TCs. The detection limits of tetracycline, terramycin and chlortetracycline were 0.2367, 0.3739 and 0.2791 µM, respectively. The results of TC by fluorescence method in real water samples were in good agreement with standard Ultraviolet-visible (UV-vis) method. The N-CQDs have various potential applications including sensitive and selective detection of Fe3+ and TCs, and cellular imaging with low cytotoxicity, good biocompatibility and high permeability.

N,S-self-doped carbon quantum dots from fungus fibers for sensing tetracyclines and for bioimaging cancer cells.

In this work, nitrogen and sulfur dual-doped carbon quantum dots (N,S-CDs) from naturally renewable biomaterial fungus fibers were prepared by a biosynthesis and hydrothermal method. The N,S-CDs displayed good water solubility, excellent stability, high quantum yield (QY = 28.11%) as well as remarkable features for fluorescence quenching-based detection and cellular imaging of cancer cells. It was worth mentioning that the heteroatoms doped carbon quantum dots made from the fungus fibers had a satisfactory QY and could be used as a selective, efficient, and sensitive fluorescent probe to determine tetracyclines by the synergistic effects of static quenching and internal filtration effect. The probe demonstrated a wide linear range and low detection limit. For tetracycline, the linear range was 0.5 µM to 47.6 µM, and the corresponding detection limit was 15.6 nM. Significantly, the test papers prepared by using N,S-CDs could detect tetracyclines in aquiculture wastewater rapidly. The produced N,S-CDs did not affect the cell viability and showed great promises for cellular imaging.

Novel hydrophobic cotton fibers adsorbent for the removal of nitrobenzene in aqueous solution.

In order to improve the superhydrophobic and oil-wet properties of raw cotton fibers come from Jiangsu province, China. A novel adsorbent, hydrophobic cotton fibers (HCF) with an excellent superhydrophobic and larger length was synthesized via modified sol-gel method and examined for the removal of nitrobenzene in aqueous solution. Results show that the treated raw cotton fibers exhibited outstanding non-wettability with the WCA of 152° and the larger length of 0.2-0.4cm, which offers an opportunity to separation in for the removal of nitrobenzene. It was found that adsorption isotherm and kinetics of nitrobenzene onto HCF were well described by the Freundlich and pseudo-second-order kinetic models, respectively. The thermodynamic data showed that the nitrobenzene adsorption onto HCF was a spontaneous, endothermic and physisorption reaction. The monolayer adsorption capacity of nitrobenzene was found to be 16.85mg/g at 30°C.