Preparation of modified humic acid/TiO2/P(AA-co-AM) nanocomposite hydrogels with enhanced dye adsorption and photocatalysis.

A novel composite hydrogel with exceptional adsorption and photocatalytic properties was synthesized using modified coal-based humic acid (HA-C), modified titanium dioxide (TiO2) nanoparticles, acrylic acid (AA), and acrylamide (AM) as precursors. The modification of HA-C and TiO2 significantly enhances the structural support provided by the hydrogel for photocatalytic components. Moreover, we investigated the effects of monomer ratio, dye concentration, temperature, and pH on the material properties. Additionally, we tested the mechanical strength, swelling behavior, and reusability of the hydrogels. The composite hydrogel's adsorption performance and synergistic adsorption-photocatalytic performance were evaluated based on its removal rate for both absorbed and degraded methylene blue (MB). Remarkably, incorporating HA-C greatly improved the adsorption efficiency of the composite hydrogel for methylene blue to a maximum capacity of 1490 mg g-1. Furthermore, TiO2 nanoparticles in the structure promoted MB degradation with an efficiency exceeding 96.5%. The hydrogel exhibited excellent recoverability and reusability through nine cycles of adsorption/desorption as well as six cycles of degradation.

Preparation of high strength, self-healing conductive hydrogel based on polysaccharide and its application in sensor.

The development of cost-effective, eco-friendly conductive hydrogels with excellent mechanical properties, self-healing capabilities, and non-toxicity holds immense significance in the realm of biosensors. The biosensors demonstrate promising applications in the fields of biomedical engineering and human motion detection. A unique double-network hydrogel was prepared through physical-chemical crosslinking using chitosan (CS), polyacrylic acid (AA), and sodium alginate (SA) as raw materials. The prepared double-network hydrogels exhibited exceptional mechanical properties, as well as self-healing and conductive capabilities. Polyacrylic acid as the first layer network, while chitosan and sodium alginate were incorporated to establish the second layer network through electrostatic interactions, thereby imparting self-healing and self-recovery properties. The hydrogel was subsequently immersed in the salt solution to induce network winding. The mechanical robustness of the hydrogel was significantly enhanced through synergistic coordination of covalent and non-covalent interactions. When the concentration of sodium alginate was 20 g/L, the double-network hydrogel exhibits enhanced mechanical properties, with a tensile fracture stress of up to 1.31 MPa and a strength of 4.17 MPa under 80% compressive deformation. Furthermore, the recovery rate of this double-network hydrogel reached an impressive 89.63% within a span of 30 min. After 24 h without any external forces, the self-healing rate reached 26.11%, demonstrating remarkable capabilities in terms of self-recovery and self-healing. Furthermore, this hydrogel exhibited consistent conductivity properties and was capable of detecting human finger movements. Hence, this study presents a novel approach for designing and synthesizing environmentally friendly conductive hydrogels for biosensors.

Preparation and Photocatalytic Performance of Sodium Alginate/Polyacrylamide/Polypyrrole-TiO2 Nanocomposite Hydrogels.

The application of photocatalysis technology in environmental pollution treatment has garnered increasing attention, and enhancing the photocatalytic efficiency and recyclability of photocatalysts represents a pivotal research focus for future endeavors. In this paper, polypyrrole titanium dioxide nanocomposite (PPy-TiO2) was prepared using in situ polymerization method and dispersed in sodium alginate/polyacrylamide (SA/PAM) hydrogel matrix to prepare SA/PAM/PPy-TiO2 nanocomposite hydrogels. The nanocomposite hydrogels were characterized by XPS, FT-IR, XRD, TGA, SEM, and TEM. The results showed that the composite materials were successfully prepared and PPy-TiO2 was uniformly dispersed in the hydrogel matrix. The incorporation of PPy in the SA/PAM/TiO2 composite hydrogel resulted in enhanced visible light absorption, reduced recombination efficiency of photoelectron-hole pairs in TiO2, and facilitated the photocatalytic degradation of methylene blue (MB) and methyl orange (MO) under sunlight irradiation. The photocatalytic efficiency of the composite hydrogel for MB was nearly 100%, whereas for MO, it reached 91.85% after exposure to sunlight for 120 min. In comparison with nano-TiO2 and PPy-TiO2, the SA/PAM/PPy-TiO2 nanocomposite hydrogel exhibited a higher degradation rate of MB and demonstrated ease in separation and recovery from the reaction solution. Furthermore, even after undergoing five cycles of recycling, there was no significant decrease observed in photodegradation efficiency.

Synthesis of new functionalized magnetic nano adsorbents and adsorption performance for Hg(II) ions.

Fe3O4@SiO2-NH-nNG-SPTZ (including Fe3O4@SiO2-NH-2NG-SPTZ, Fe3O4@SiO2-NH-3NG-SPTZ) were prepared by 2-mercapto-5-(4-pyridyl)-1,3,4-thiadiazole and the reaction products of 3, 6-dichloropyridazine and cyanuric chloride with Fe3O4@SiO2-NH2 respectively. Fe3O4@SiO2-S-nNG-SPTZ (including Fe3O4@SiO2-S-2NG-SPTZ, Fe3O4@SiO2-S-3NG-SPTZ) were prepared by 2-mercapto-5-(4-pyridyl)-1,3,4-thiadiazole and the reaction products of 3, 6-dichloropyridazine and cyanuric chloride with Fe3O4@SiO2-SH respectively. Four novel adsorbents were characterized by SEM, TEM, FT-IR and XRD. Hg(II) ions removal efficiency of these adsorbents were more than 95%, in 15-20 min, at pH 7.0-8.0. It is easy to separate these adsorbents that adsorb mercury ions from the solution through magnets. These adsorbents have similar adsorption mechanism and have application value in the treatment of mercury ions in sewage and are worth studying.

Photopolymerisation and characterization of maleylatedcellulose-g-poly(acrylic acid) superabsorbent polymer.

A novel biodegradable superabsorbent polymer has been prepared from maleylated cotton stalk cellulose (MCSC) crosslinker and acrylic acid (AA) by ultraviolet (UV) photopolymerization in aqueous solution at room temperature, and irgacure 651 as a photoinitiator. The resulting superabsorbent was characterized by FT-IR, (1)H NMR, SEM and TGA. The effects of preparation conditions such as degree of substitution (DS), amount of maleylated cotton stalk cellulose, exposed time, photoinitiator amount and monomer concentration on the water absorbency and the monomer conversion in graft were evaluated. The swelling kinetics, salt-resistance, water retention capacity and biodegradability of the MCSC-g-PAA superabsorbent were investigated. It was found that, the obtained superabsorbent have good swelling degree that greatly affected by its composition and preparation conditions. Owing to its considerable good water retention capacity, being economical and environment-friendly, it might be useful for its application in agriculture field.