Calcium Alginate Research Articles

Immobilization of <i>Azospirillum</i> Bacteria on Various Carriers

A significant part of research in environmentally friendly agroindustrial production is aimed at immobilized bacterial preparations with retained capacity for active growth without loss of metabolic activity both during immobilization and after long-term storage and biotechnological use. In the present work, immobilization of members of the genus Azospirillum on natural and synthetic carriers was investigated. Efficiency of immobilization of the cells of A. brasilense strain SR80 in alginate hydrogel and vermiculite was investigated. Proliferative and metabolic activities of immobilized preparations were investigated. The prospects of using vermiculite and calcium alginate as matrices for Azospirillum immobilization are shown.

Visible-light-driven calcium alginate hydrogel encapsulating BiOBr0.75I0.25 for efficient removal of oxytetracycline from wastewater

Oxytetracycline (OTC), a widely used antibiotic, poses significant environmental risks due to its persistence in ecosystems. This study introduces a visible-light-driven photocatalytic hydrogel system for effectively removing OTC from wastewater. The system employs calcium alginate (CA) hydrogel beads encapsulating a BiOBr0.75I0.25 solid solution, which utilizes the synergistic effects of adsorption and visible-light-driven photocatalysis. The BiOBr0.75I0.25 solid solution photocatalyst was synthesized via a solvothermal method, while CA hydrogel beads encapsulating BiOBr0.75I0.25 were prepared through ionic gelation of sodium alginate with calcium chloride. The novel hydrogel, CA-BiOBr0.75I0.25, demonstrated rapid adsorption, capturing over 50 % of OTC within 30 min and achieving a 90.92 % degradation rate within 60 min under visible light. This performance is associated with the unique petal-like structure of BiOBr0.75I0.25 and the high surface area of the hydrogel, facilitating efficient charge separation and radical generation critical for photocatalytic activity. Additionally, the system showed excellent stability and reusability, maintaining an 83 % removal efficiency after five cycles. These findings highlight the potential of this novel hydrogel as a sustainable solution for advanced wastewater treatment technologies.

Synthesis, characterization and photocatalytic activity of alginate based hybrid material for efficient degradation of organic pollutants under UV light and sunlight irradiation

This study reports the development of alginate based hybrid material (Alg/CuO-gC₃N₄) with copper oxide (CuO) and graphitic carbon nitride (gC₃N₄). The Alg/CuO-gC₃N₄ hydrogel bead was prepared by two step process is as follows: formation of CuO-gC₃N₄ by co-precipitation method and incorporation of CuO-gC₃N₄ in the calcium alginate (Alg) by ionotropic gelation method. The structural and morphological features of the Alg/CuO-gC₃N₄ was characterized using different techniques namely Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Thermogravimetric analysis (TGA), UV Diffuse Reflectance spectroscopy (UV-DRS) and Scanning electron microscopy (SEM). The photocatalytic activity of the Alg/CuO-gC₃N₄ was extensively evaluated by degrading methylene blue (MB) under UV–vis and sunlight irradiation. The influence of various parameters like pollutant type, initial dye concentration, catalyst dosage, effect of pH, light intensity and reusability was investigated. The Alg/CuO-gC₃N₄ achieved a maximum degradation efficiency of 86.26 % and 85.15 % for MB at a dye concentration of 1 × 10−5 M under UV–vis and sunlight irradiation respectively, within 60 min using 0.3 wt% of catalyst dosage. The Alg/CuO-gC₃N₄ exhibited excellent stability and reusability over multiple cycles. Additionally, the incorporation of CuO-gC₃N₄ in alginate facilitates in reducing the bandgap (2.54 to 2.28 eV) for efficient charge separation, further enhancing the overall photocatalytic activity.

Field evaluations of biodegradable boric acid hydrogel baits for the control of Argentine ants: Promising results in vineyards and citrus orchards

Argentine ants are a major pest in California. In this study, a biodegradable calcium alginate hydrogel with an aqueous boric acid bait was tested against Argentine ant populations in a citrus orchard and a vineyard. A new continuous method was developed to produce large quantities of hydrogel bait for the field test. Foraging activity levels of ants were compared between baited and untreated zones. For both study sites, four to five monthly bait applications throughout summer provided a greater than 80% reduction in ant activity. Based on spatial analyses by distance indices, the baited areas were characterized by gaps (areas with lower ant counts) and the untreated control zones were characterized by patches (areas with higher ant counts). This indicated area-wide suppression of Argentine ants. For the citrus orchard, post-baiting panel trap monitoring showed reductions of both ants and Asian citrus psyllid in the baited zone compared to the control. For the vineyard, mid-season soil analyses indicated that the impact of boric acid baiting on soil boron concentration was negligible. In sum, the calcium alginate hydrogel bait with boric acid as an active ingredient may provide a promising solution for Argentine ant baiting.

One-Step Formation of Pickering Double Emulsion Costabilized by Hydrophobic Silica Nanoparticles and Sodium Alginate.

Pickering double emulsions exhibit higher stability and biocompatibility compared with surfactant-stabilized double emulsions. However, tailored synthesis of particle stabilizers with appropriate wettability is time consuming and complicated and usually limits their large-scale adoption. Using binary stabilizers may be a simple and scalable strategy for Pickering double emulsion formation. Herein, commercially available hydrophobic silica nanoparticles (SNPs) and sodium alginate (SA) as binary stabilizers are used to prepare O/W/O Pickering double emulsions in one-step emulsification. The influence of system composition on double emulsion preparation is identified by optical microscopy, confocal laser scanning microscopy, and interfacial tension and water contact angle analyses. The formation of the O/W/O Pickering double emulsion depends critically on the aqueous phase viscosity and occurrence of emulsion inversion. Both hydrophobic SNPs and SA adsorb at the droplet surface to provide a steric barrier, while SA also reduces interfacial tension and increases aqueous phase viscosity, giving double emulsion long-term stability. Their microstructure and stability are controlled by adjusting the SA concentration, water-oil volume ratio, concentration and wettability of the particle stabilizer, and oil type. As a demonstration, the middle layer of the as-prepared O/W/O Pickering double emulsions can be cross-linked in situ with calcium ions to produce calcium alginate porous microspheres. We believe that our strategy for double emulsion formation holds great potential for practical applications in food, cosmetics, or pharmaceuticals.

Biocomposite Material Based on Lactococcus lactis sp. Immobilized in Natural Polymer Matrix for Pharmaceutical Removal from Aqueous Media.

Ecosystems are negatively impacted by pharmaceutical-contaminated water in different ways. In this work, a new biosorbent obtained by immobilizing Lactococcus lactis in a calcium alginate matrix was developed for the removal of pharmaceuticals from aqueous solutions. Ethacridine lactate (EL) was selected as the target drug. Lactococcus Lactis biomass was chosen for the biosorbent synthesis for two reasons: (i) the microbial biomass used in the food industry allows the development of a low-cost biosorbent from available and renewable materials, and (ii) there is no literature mentioning the use of Lactococcus Lactis biomass immobilized in natural polymers as a biosorbent for the removal of pharmaceuticals. The characterization of the synthesized biosorbent named 5% LLA was performed by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) analysis. Additionally, particle size and the point of zero charge were established. Batch biosorption investigations showed that using 5% LLA at an initial pH of 3.0 and a biosorbent dose of 2 g/L resulted in up to 80% EL removal efficiency for all EL initial concentrations (20-60 mg/L). Four equilibrium isotherms, given in the order of Redlich-Peterson > Freundlich > Hill > Temkin, are particularly relevant for describing the experimental data for EL biosorption on the 5% LLA biosorbent using correlation coefficient values. Kinetic parameters were determined using kinetic models such as pseudo-first-order, pseudo-second-order, Elovich, Avrami and Weber-Morris. The pseudo-second-order kinetics model provides the greatest fit among the evaluated equations, with correlation coefficients greater than 0.99. According to the study's findings, the developed biocomposite is a potentially useful material for the removal of pharmaceuticals from aqueous matrices.

Industrial dye absorption and elimination from aqueous solutions through bio-composite construction of an organic framework encased in food-grade algae and alginate: Adsorption isotherm, kinetics, thermodynamics, and optimization by Box–Behnken design

A potential bio-adsorbent material for removing Rhodamine B (RB) from aqueous solution is Ru-MOF@FGA/CA beads. The adsorption capability of the material is probably enhanced by the use of a natural substance made of food-grade algae (FGA) and calcium alginate (CA), which has been cross-linked and loaded with ruthenium metal-organic frameworks (Ru-MOF). The Ru-MOF@FGA/CA beads were analyzed by XPS, PXRD, FT-IR, and SEM. The nitrogen adsorption-desorption isotherm analysis of the Ru-MOF@FGA/CA beads before and after the adsorption of RB revealed that had a surface area of 682 m2/g, a pore size of 2.92 nm, and a pore volume of 1.62 cc/g, that decreased after adsorption as the surface area reduced to 468.62 m2/g, while the pore volume reduced to 0.76 cc/g. indicating that the RB molecules occupied the available space within the pores of the material. The decrease in both surface area and pore volume specifies that the Ru-MOF@FGA/CA beads' pores were able to effectively adsorb the RB molecules. The adsorption of RB against the Ru-MOF@FGA/CA beads is affected by pH, adsorbent dose, starting RB concentration, and salinity. Controlling these factors can enhance the adsorption capability and effectiveness of the beads for RB removal. With an adsorption energy of 22.6 kJ/mol, the adsorption of RB onto the Ru-MOF@FGA/CA beads was determined to be a chemisorption process, demonstrating a strong bond among the adsorbent and the adsorbate. The pseudo-second-order kinetics and Langmuir isotherms were used to suit the adsorption process. Because the adsorption procedure was endothermic, it increased as the temperature increased. By using this information, the adsorption conditions may be improved, and the beads' ability to absorb RB can be increased. Up to six reuses of the Ru-MOF@FGA/CA beads are possible without affecting their chemical makeup and maintaining analogous PXRD and FT-IR data after each reuse. The adsorption process can be optimized through the application of the Box–Behnken design (BBD) approach and may entail H-bonding, electrostatic forces, n-π stacking, and pore filling. The exceptional stability of the beads makes them useful for creating long-lasting and efficient adsorbents that remove contaminants from water.

Innovative Microbial Immobilization Strategy for Di-n-Butyl Phthalate Biodegradation Using Biochar-Calcium Alginate-Waterborne Polyurethane Composites.

Di-n-butyl phthalate (DBP) is a prevalent phthalate ester widely used as a plasticizer, leading to its widespread presence in various environmental matrices. This study presents an innovative microbial immobilization strategy utilizing biochar, calcium alginate (alginate-Ca, (C12H14CaO12)n), and waterborne polyurethane (WPU) composites to enhance the biodegradation efficiency of DBP. The results revealed that rice husk biochar, pyrolyzed at 300 °C, exhibits relatively safer and more stable physical and chemical properties, making it an effective immobilization matrix. Additionally, the optimal cultural conditions for Bacillus aquimaris in DBP biodegradation were identified as incubation at 30 °C and pH 7, with the supplementation of 0.15 g of yeast extract, 0.0625 g of glucose, and 1 CMC of Triton X-100. Algal biotoxicity results indicated a significant decrease in biotoxicity, as evidenced by an increase in chlorophyll a content in Chlorella vulgaris following DBP removal from the culture medium. Finally, microbial community analysis demonstrated that encapsulating B. aquimaris within alginate-Ca and WPU layers not only enhanced DBP degradation, but also prevented ecological competition from indigenous microorganisms. This novel approach showcases the potential of agricultural waste utilization and microbial immobilization techniques for the remediation of DBP-contaminated environments.

Enhancing immobilized Chlorella vulgaris growth with novel buoyant barium alginate bubble beads

Microalgae immobilization in alginate beads shows promise for biomass production and water pollution control. However, carrier instability and mass transfer limitations are challenges. This study introduces buoyant barium alginate bubble beads (BABB), which offer exceptional stability and enhance Chlorella vulgaris growth. In just 12 days, compared to traditional calcium alginate beads, BABB achieved a 20 % biomass increase while minimizing cell leakage and simplifying harvesting. BABB optimization involved co-immobilization with BG-11 medium, enrichment of CO2 in internal bubbles, and the integration of Fe nanoparticles (FeNPs). In the open raceway pond reactor, these optimizations resulted in a 39 % increase in biomass over 7 days compared to the unoptimized setup in closed flasks. Furthermore, enhancements in pigment and organic matter production were observed, along with improved removal of ammonia nitrogen and phosphate. These results highlight the overall advantages of BABB for microalgae immobilization, offering a scientific foundation for their effective utilization.

Development of a tobramycin-loaded calcium alginate microsphere/chitosan composite sponge with antibacterial effects as a wound dressing

Traditional dressings exhibit several disadvantages, as they frequently lead to bacterial infections, cause severe tissue adhesion and perform a relatively single function. Therefore, in this study, a composite sponge dressing with antibacterial properties and excellent physicochemical properties was developed. Six groups of tobramycin-loaded calcium alginate microspheres were prepared by changing the amount of tobramycin added, and the optimal group was selected. Then, seven groups of tobramycin-loaded calcium alginate microsphere/chitosan composite sponges were fabricated via a solvent blending process and a freeze-drying method. The surface morphology, physicochemical properties, in vitro degradation properties, in vitro drug release properties, antibacterial properties and cytotoxicity of the composite sponges were examined. Group 3.0 contained the best microspheres with the largest drug loading capacity, good swelling performance and cumulative drug release rate, obvious and sustained antibacterial activity, and good cytocompatibility. The tobramycin-loaded calcium alginate microsphere/chitosan composite sponges exhibited three-dimensional porous structures, and their porosity, swelling rate, water absorption and water retention rates and water vapor transmission rate met the standards needed for an ideal dressing. The comprehensive performance of the sponge was best when 20 mg of drug-loaded microspheres was added (i.e. group 20). The cumulative drug release rate of the sponge was 29.67 ± 4.14% at 7 d, the diameters of the inhibition zones against the three bacteria were greater than 15 mm, and L929 cell proliferation was promoted. These results demonstrated that the tobramycin-loaded calcium alginate microsphere/chitosan composite sponge with 20 mg of tobramycin-loaded microspheres shows promise as a dressing for infected wounds.

Construction and characterization of alginate/calcium β-hydroxy-β-methylbutyrate hydrogels: Effect of M/G ratios and calcium ion concentration

Calcium β-hydroxy-β-methylbutyrate (CaHMB), a functional calcium salt, is used to maintain and improve muscle health. Here, a new hydrogel material prepared from alginate (ALG) with three M/G ratios (1:1, 2:1, and 1:2) and CaHMB (0–2 mg/mL) was investigated. CaHMB regulates the formation and properties of ALG hydrogels through chelation and hydrogen bonding. When the M/G ratio was 2:1, the anionic groups of CaHMB containing carboxyl and hydroxyl groups formed hydrogen bonds with the polysaccharide chains, hindering the capture of Ca2+ by the G-residue fragments of ALG, which in turn retarded the gelation process. The noncalcium cross-linked polysaccharide chain structure of ALG and the anionic group of CaHMB also affected the water distribution in the hydrogel, especially when M residue content ≥G residue content. Lower M/G ratios and higher CaHMB concentrations could increase the number of “egg box” crosslinking junctions of calcium alginate, and the microstructure was denser in the gel pores, resulting in a stronger gel strength and more free water bound in the gel matrix. This study provides a theoretical and methodological basis for the design of novel hydrogels by studying the crosslinking features of ALG/CaHMB.

Magnesium vs. sodium alginate as precursors of calcium alginate: Mechanical differences and advantages in the development of functional neuronal networks

Calcium alginate is one of the most widely employed matrices in regenerative medicine. A downside is its heterogeneity, due to the poorly controllable character of the gelation of sodium alginate (NaAlg), i.e. the commonly used alginate salt, with calcium. Here, we have used magnesium alginate (MgAlg) as an alternative precursor of calcium alginate. MgAlg coils, more compact and thus less entangled than those of NaAlg, allow for an easier diffusion of calcium ions, whereas Mg is exchanged with calcium more slowly than Na; this allows for the formation of a material (Ca(Mg)Alg) with a more reversible creep behaviour than Ca(Na)Alg, due to a more homogeneous – albeit lower - density of elastically active cross-links. We also show that Ca(Mg)Alg supports better than Ca(Na)Alg the network development and function of embedded (rat cortical) neurons: they show greater neurite extension and branching at 7 and 21 days (Tubb3 and Map2 immunofluorescence) and better neuronal network functional maturation / more robust and longer-lasting activity, probed by calcium imaging and microelectrode array electrophysiology. Overall, our results unveil the potential of MgAlg as bioactive biomaterial for enabling the formation of functional neuron-based tissue analogues.

Highly efficient removal of amine via ion bonds based on renewable graphene templated poly-acids generated via reversible addition-fragmentation chain transfer polymerizations

As the only alkaline gas in the atmosphere, ammonia (NH3) is a promoter of atmospheric haze generation. It is also one of the main indoor air pollutants, and has an irritating and corrosive effect on the upper respiratory tract of the human body. Here, we report the synthesis of polymer composites with reduced graphene oxide (rGO) as template for the efficient removal of ammonia via ion bonds under ambient conditions. rGO has an ultra-large specific surface area for immobilizing pyrene-terminated poly-acids (PyPAA and PyPSSA) to obtain polymer/rGO composites (PyPAA/rGO and PyPSSA/rGO) which are cross-linked by calcium alginate (CA) to form a three-dimensional highly porous spherical aerogel (polymer/rGO/CA) platelet. Reversible addition-fragmentation chain transfer (RAFT) polymerization is used to synthesize two poly-acids with acidic groups, which can react with NH3 to form ammonium salts via ionic bonding, resulting in the chemical removal of NH3 without the generation of any other by-products. Impressively, 100 mg of PyPAA/rGO and PyPSSA/rGO composites could remove 18.7 mg and 12 mg of NH3, respectively. The current methodology to prepare poly-acids/rGO composites provides a means for efficient removal of NH3 pollutant.

Study on Adsorption of Cd in Solution and Soil by Modified Biochar-Calcium Alginate Hydrogel.

Contamination with cadmium (Cd) is a prominent issue in agricultural non-point source pollution in China. With the deposition and activation of numerous Cd metal elements in farmland, the problem of excessive pollution of agricultural produce can no longer be disregarded. Considering the issue of Cd pollution in farmland, this study proposes the utilization of cross-linked modified biochar (prepared from pine wood) and calcium alginate hydrogels to fabricate a composite material which is called MB-CA for short. The aim is to investigate the adsorption and passivation mechanism of soil Cd by this innovative composite. The MB-CA exhibits a higher heavy metal adsorption capacity compared to traditional biochar and hydrogel due to its increased oxygen-containing functional groups and heavy metal adsorption sites. In the Cd solution adsorption experiment, the highest Cd2+ removal rate reached 85.48%. In addition, it was found that the material also has an excellent pH improvement effect. Through the adsorption kinetics experiment and the soil culture experiments, it was determined that MB-CA adheres to the quasi-second-order kinetic model and is capable of adsorbing 35.94% of Cd2+ in soil. This study validates the efficacy of MB-CA in the adsorption and passivation of Cd in soil, offering a novel approach for managing Cd-contaminated cultivated land.

Survivability and characterization of the biofilm-like probiotic Pediococcus pentosaceus encapsulated in calcium alginate gel beads

Probiotic bacteria have been well-known to provide health benefits to human beings. However, several harsh conditions have threatened their survival rate during processing, storage, and transit through the gastrointestinal tract (GIT). This study investigated the survivability of biofilm-producing Pediococcus pentosaceus encapsulated in calcium alginate gel beads (CAGBs) against harsh conditions. The present study successfully produced biofilms-in situ culture of P. pentosaceus in the CAGBs (CAGB-bio-situ). The subsequently formed biofilms showed high survivability to the GIT environment (50%–74%), refrigerator storage (88.6%), and pH 2 (30.7%). In addition, the Fourier transform infrared spectroscopy (FTIR) revealed that no new chemical bonds were formed between the sodium alginate and the bacterial cell. Furthermore, the water content of the CAGBs averaged 10.06%, which was considered acceptable. A single-step weight loss was observed in the thermogravimetric analysis (TGA) of CAGBs, while CAGB-bio-situ showed high thermal stability. Moreover, scanning electron microscopy (SEM) displayed bacteria aggregation on the beads surface in CAGB-bio-situ. As an alternative approach, this study speculates that the ability of P. pentosaceus to form biofilm would benefit from additional protection of CAGBs, which could serve as a fourth-generation approach to protect probiotics.

Synthesis of calcium alginate hydrogel loaded with platelet rich plasma for use in regenerative medicine and morphological investigation using field emission scanning electron microscope

Synthesis of calcium alginate hydrogel loaded with platelet rich plasma for use in regenerative medicine and morphological investigation using field emission scanning electron microscope

Green and facile fabrication of robust calcium alginate sponges via thermally bonded nonwoven induced freeze-drying for dressing applications

Alginate sponges have been widely studied in areas of wound healing, drug release, tissue engineering, and wastewater treatment due to their potential biological activity, biocompatibility, high porosity, and large surface area. However, their poor mechanical properties greatly limit the practical applications of alginate sponge. In this study, a structurally controllable and high-performance sponge material preparation strategy was proposed by optimizing the structure of the freeze-dried calcium alginate (CA) sponge using fluffy and porous thermally bonded nonwovens (NWs). The performance of composite sponges (CA@NWs) prepared at different pre-freezing temperatures and concentrations were tested. The results showed that the NWs skeleton could improve the formation structure and size stability of the freeze-dried CA sponge, making it have good fluid absorption, moisture permeability, moisture retention, and wet state mechanical properties. The RF-1.0-CA@NWs sponge had the highest fluid absorption rate of 1415 %. The wet state RF-1.5-CA@NWs sponge had tensile strengths of 1.913 MPa and 0.465 MPa in the MD and CD directions, respectively, which was about 95 times higher than that of the wet state pure CA sponge.

Transforming the Stability, Encapsulation, and Sustained Release Properties of Calcium Alginate Beads through Gel-Confined Coacervation.

Calcium alginate (Ca2+/alginate) gel beads find use in diverse applications, ranging from drug delivery and tissue engineering to bioprocessing, food formulation, and agriculture. Unless modified, however, these gels have limited stability in alkaline media (including phosphate buffers), and their high solute permeability limits their ability to efficiently encapsulate and slowly release water-soluble small molecules. Here, we show how these limitations can be addressed by mixing the alginate solutions used in the bead preparation with the nontoxic anionic polymer polyphosphate (PP). Upon complexing Ca2+ ions, PP undergoes complex coacervation (i.e., liquid/liquid phase separation into a Ca2+/PP-rich coacervate phase and a dilute supernatant phase). At lower PP concentrations, the Ca2+/PP coacervate appears to simply remain dispersed within the beads. Though its presence makes the beads more stable in alkaline media (phosphate-buffered saline and seawater), it has little impact on the bead stiffness, morphology, and (at least in the absence of substantial payload/coacervate association) encapsulation and release properties. When the PP concentrations exceed a critical value, however, Ca2+/PP coacervation within the gelling Ca2+/alginate beads collapses the resulting beads into more compact, interpenetrating polymer networks. Besides their enhanced stability to alkaline environments, these hybrid beads exhibit irregular morphologies with wrinkled and dimpled surface structures and macroscopic (closed) internal pores, and their collapse into these polymer-rich networks also makes them significantly stiffer than their PP-free counterparts. Crucially, these beads also exhibit a much lower solute permeability, which enables highly efficient encapsulation and multiday release of water-soluble small molecules (with the beads encapsulating >90% of the added model payload and sustaining its release over 3-5 d). Collectively, these findings provide a mild and simple (single-step) pathway to generating ionically cross-linked alginate beads with significantly enhanced stability, encapsulation efficiency, and sustained release.

Fabrication of Uniform Anionic Polymeric Nanoplatelets as Building Blocks for Constructing Conductive Hydrogels with Enhancing Conductive and Mechanical Properties.

Conductive hydrogels play a crucial role in advancing technologies like implantable bioelectronics and wearable electronic devices, owing to their favorable conductivity and appropriate mechanical properties. Here, a novel bottom-up approach is reported for crafting conductive nanocomposite hydrogels to achieve enhancing conductive and mechanical properties. In this approach, new poly(ɛ-caprolactone)-based block copolymers with sulfonic groups are first synthesized and self-assembled into uniform polyanionic nanoplatelets. Subsequently, these negatively charged nanoplatelets, with sulfonic groups on the surface, are employed as nanoadditives for the polymerization of 3,4-ethylenedioxythiophene (EDOT), resulting in poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS)/nanoplatelet complex with 3.8 times enhanced electrical conductivity compared with their counterparts prepared using block copolymers (BCPs). Blending the (PEDOT:PSS)/nanoplatelet complex with calcium alginate, nanocomposite hydrogels are successfully prepared. In comparison with hydrogels with (PEDOT:PSS)/BCP complexes prepared by a top-down method, the nanocomposite hydrogels are found to show twice as strong mechanical strength and 1.6 times higher conductivity. This work provides valuable insights into the bottom-up construction of conductive hydrogels for bioelectronics using well-controlled polymeric nanoplatelets.

TiO2 deposited dual functional hydrogel coatings with superhydrophilic and photocatalytic properties for efficient oil/water separation and dye photodegradation

Hydrogel coatings have been applied in oil/water separation owing to the underwater superoleophobic and anti-oil fouling property. However, the intrinsic relatively poor mechanical performance of hydrogel coatings and inevitably polluted by organic pollutants induce the separation performance reduction in the long-term operation and even possibly cause the coatings to peel off. In this work, we developed a simple and robust TiO2 deposited polyacrylamide-sodium alginate (TiO2@PAS) composite hydrogel coating with underwater superoleophobic and dye photodegradation abilities. PDA/TiO2 nanoparticles were deposited on the substrate surface through the mussel inspired chemistry strategy. Moreover, Polyacrylamide and calcium alginate were crosslinked into the double network hydrogel to enhance mechanical performance. The prepared hydrogel coating was introduced onto different substrates to endow the coated substrates with robust superwetting and anti-oil fouling properties. Separation efficiency of TiO2@PAS hydrogel coated copper mesh for oil/water mixtures reached 99.1% after 50 cycle separation tests. The hydrogel coated PVDF membrane was prepared through the same method and separation efficiency for oil-in-water emulsion keeps above 99.3% during multiple cycles separation. Moreover, the photocatalysis active TiO2 nanoparticles allowed the TiO2@PAS composite hydrogel coating to degrade the organic dye methylene blue (MB) through the photo-Fenton-like photodegradation process with degradation efficiency as high as 98.7%. Notedly, the TiO2@PAS hydrogel coating shows robust superwetting performance even underwent abrasion test and acid-base immersing, which has the potential for adapting extreme operating condition. Overall, the study on the TiO2@PAS composite hydrogel coatings provides a general and simple design strategy for superwetting and photocatalytic hydrogel coatings for multi-demand water treatment application.