Efficient degradation of bisphenol A and amino black 10B by magnetic composite FeO@MOF-74 as catalyst.

Metal-organic frameworks (MOFs) exhibit high chemical stability and porosity, and have been widely applied in various fields including selective adsorption and separation, sensors, and catalysis. When combined with FeO, they effectively address issues such as aggregation of FeO particles and the difficulty in recovering MOFs as catalysts. Therefore, in this study, we used a simple solvothermal method as a catalyst to synthesize a high specific surface area magnetic composite FeO@MOF-74, which was used to catalyze the degradation of bisphenol A (BPA) and amino black 10B in wastewater.

Multiperformance PAM/PVA/CaCO Hydrogel for Flexible Sensing and Information Encryption.

Currently, the development of hydrogels with excellent mechanical properties (elasticity, fatigue resistance, etc.) and conductive properties can better meet their needs in the field of flexible sensor device applications. Generally, hydrogels with a denser cross-linking density tend to have better mechanical properties, but the improvement in mechanical properties comes at the expense of reduced electrical conductivity.

Synthesis of Aminomethylpyridine-Decorated Polyamidoamine Dendrimer/Apple Residue for the Efficient Capture of Cd(II).

Water contamination irritated by Cd(II) brings about severe damage to the ecosystem and to human health. The decontamination of Cd(II) by the adsorption method is a promising technology. Here, we construct aminomethylpyridine-functionalized polyamidoamine (PAMAM) dendrimer/apple residue biosorbents (AP-G1.

Mechanical Properties of Low-Molecular-Weight Peptide Hydrogels Improved by Thiol-Ene Click Chemistry.

Low-molecular-weight peptide hydrogels can be formed by self-assembly through weak interactions, but the application of the hydrogel is influenced by its weak mechanical properties. Therefore, it is important to construct low-molecular-weight peptide hydrogels with excellent mechanical properties. In this work, we designed the pentapeptide molecule Fmoc-FFCKK-OH (abbreviated as FFCKK) with a sulfhydryl group, and another low-molecular-weight cross-linker ,-methylenebis(acrylamide) (MBA) was introduced to construct a hydrogel with excellent mechanical properties.

Oxidized sodium alginate/polyacrylamide hydrogels adhesive for promoting wheat growth.

Chemical modification of sodium alginate (SA) polymer chains can increase its functional group species. Sodium periodate (SP) was usually used to oxidize the hydroxyl groups on the chain of SA to aldehyde groups, the preparation of oxidized sodium alginate (OSA) using SP is not only complicated, also limits the variety of functional groups on the chain of OSA. By contrast, we have developed an innovative strategy for OSA, in which ammonium persulfate (APS) was used to oxidize SA, providing a clear elucidation of the oxidizing process and mechanism.

Synthesis of salicylaldehyde tailored PAMAM dendrimers/chitosan for adsorption of aqueous Hg(II): Performance and mechanism.

Water pollution caused by Hg(II) exerts hazardous effect to environmental safety and human health. Herein, a family of salicylaldehyde tailored poly(amidoamine) (PAMAM) dendrimers/chitosan composites (G0-S/CTS, G1-S/CTS, and G2-S/CTS) were prepared and used for the removal of Hg(II) from water solution. The adsorption performance of the as-prepared composites for Hg(II) was thoroughly demonstrated by determining various influencing factors.

Adsorption Performance of Magnetic Covalent Organic Framework Composites for Bisphenol A and Ibuprofen.

As typical environmental endocrine disruptors and nonsteroidal anti-inflammatory drugs, bisphenol A and ibuprofen in water supplies can cause great harm to the ecological environment and human health. In this study, magnetic covalent organic framework composites FeO@COF-300 were synthesized by the hydrothermal method and used to remove bisphenol A and ibuprofen from water. FeO@COF-300 could be rapidly separated from the matrix by external magnetic fields, and could selectively adsorb bisphenol A and ibuprofen in the presence of coexisting compounds such as phenol, Congo red, and amino black 10B.

Synthesis of functional poly(amidoamine) dendrimer decorated apple residue cellulose for efficient removal of aqueous Hg(II).

Water pollution caused by Hg(II) exerts hazardous effect to the environment and public health. The design and fabrication of eco-friendly bioadsorbents for efficient removal of Hg(II) from aqueous solution is a promising strategy. Herein, a series of bioadsorbents were synthesized by the decoration of apple residue cellulose with different generation (G) Schiff base functionalized poly(amidoamine) (PAMAM) dendrimers (SA-G0/CE, SA-G1.

Synthesis of hyperbranched polyamine dendrimer/chitosan/silica composite for efficient adsorption of Hg(II).

The pollution of water system with Hg(II) exerts hazardous effect to ecosystem and public health. Adsorption is considered to be a promising strategy to remove Hg(II) from aqueous solution. Herein, hyperbranched polyamine dendrimer/chitosan/silica composite (SiO-FP) was synthesized for the adsorption of aqueous Hg(II).

Feasible synthesis of bifunctional polysilsesquioxane microspheres for robust adsorption of Hg(II) and Ag(I): Behavior and mechanism.

The pollution of Hg(II) and Ag(I) to water system exerts hazardous effect to aquatic ecosystem and public security. Simple strategy for constructing adsorbents to efficient remove them is greatly desired. Thus, a series of thiol and amino groups containing bifunctional polysilsesquioxanes (ASPSS) microspheres with adjustable porous structure and functional group content were synthesized by one-step feasible sol-gel process.

Direct Synthesis of Sulfur-Decorating PAMAM Dendrimer/Mesoporous Silica for Enhanced Hg(II) and Cd(II) Adsorption.

Water security caused by heavy metals poses a deleterious hazard to public health and the ecological system. The construction of adsorbents by polyamidoamine (PAMAM) dendrimers for efficient removal of metal ions has attracted considerable interest. However, the general method for the fabrication of these adsorbents was achieved by the surface chemical modification of the substrates with PAMAM dendrimer, which usually causes the defects of low density and uneven distribution of the dendrimer, the blocking of pores, and reducing the adsorption performance.

Peptide Hydrogel with Antibacterial Performance Induced by Rare Earth Metal Ions.

Metal ion-induced peptide assembly is an interesting field. As compared to traditional antibacterial Ag, rare earth metal ions possess the advantage of antibacterial performance with photostability and low toxicity. Herein, a new peptide Fmoc-FFWDD-OH was designed and synthesized, which could form a stable hydrogel induced by rare earth metal ions, including Tb, Eu, and La.

Drosera-Inspired Dual-Actuating Double-Layer Hydrogel Actuator.

Drosera is a small insectivorous plant whose antennae can fold up, encircle, and prey. The rapid movement of the antennae is achieved by the synergistic effect of a double-layer structure with the antennae contracts on the front and expands on the back. In this work, a drosera-inspired dual-actuating double-layer hydrogel actuator is proposed, in which the temperature-responsive poly(N, N-diethyl acrylamide) (PDEAAm) layer acts as the main actuation layer and a moisture-responsive poly(acrylamide) (PAAm) layer acts as the auxiliary actuation layer.

Advances of peptides for antibacterial applications.

In the past few decades, peptide antibacterial products with unique antibacterial mechanisms have attracted widespread interest. They can effectively reduce the probability of drug resistance of bacteria and are biocompatible, so they possess tremendous development prospects. This review provides recent research and analysis on the basic types of antimicrobial peptides (including poly (amino acid)s, short AMPs, and lipopeptides) and factors to optimize antimicrobial effects.

Single network double cross-linker (SNDCL) hydrogels with excellent stretchability, self-recovery, adhesion strength, and conductivity for human motion monitoring.

Hydrogels, as a kind of soft materials, are good candidates for smart skin-like materials. A double network is usually fabricated to improve the mechanical properties of hydrogels, and involves two different kinds of networks. In this work, a novel strategy for preparing single network double cross-linker (SNDCL) hydrogels was proposed and the prepared hydrogels exhibited excellent mechanical properties, including stretchability, compressibility, self-recovery, adhesion, shape memory and mechanical strength.

Surface-initiated PET-ATRP and mussel-inspired chemistry for surface engineering of MWCNTs and application in self-healing nanocomposite hydrogels.

A green strategy by integrating surface-initiated metal-free photoinduced electron transfer-atom transfer radical polymerization (PET-ATRP) with mussel-inspired polydopamine (PDA) chemistry, was used to fabricate multi-walled carbon nanotubes (MWCNTs)/poly(4-vinylpyridine) (P4VP) nanocomposites. Self-healing nanocomposite hydrogels were facilely designed with these nanocomposites through dynamic supramolecular interactions. Using mussel-inspired PDA chemistry from MWCNTs, nanocomposites (MWCNTs@PDA-P4VP) were successfully prepared by metal-free PET-ATRP with MWCNTs@PDA-Br as an initiator, rhodamine B as photocatalyst, 4-vinylpyridine (4VP) as monomer, respectively.

Removal of Cr(III) from aqueous solution by silica-gel/PAMAM dendrimer hybrid materials.

Water pollution caused by Cr(III) is a serious environmental problem which bring adverse effect to environmental protection and public safety. Efficient removal of Cr(III) from aqueous solution is important for the remediation of Cr(III) pollution. Herein, a series of silica-gel/polyamidoamine (PAMAM) dendrimer hybrid materials (SG-G0~SG-G4.

Fabrication of dual network self-healing alginate/guar gum hydrogels based on polydopamine-type microcapsules from mesoporous silica nanoparticles.

In this manuscript, dual network self-healing alginate/guar gum hydrogels with polydopamine-type microcapsules from mesoporous silica nanoparticles were facilely prepared through one-pot method. Glutaraldehyde (GA) was used as a crosslinking agent to crosslink guar gum and sodium alginate, respectively. Metal-ligand interactions as reversible non-covalent bonds make the dual network hydrogels have a high degree of self-healing ability, which FeCl·6HO was coordinated with sodium alginate and polydopamine on the surface of microcapsules, respectively.

RAFT-mediated Pickering emulsion polymerization with cellulose nanocrystals grafted with random copolymer as stabilizer.

The synthesis of a RAFT-mediated Pickering emulsion was firstly achieved by using cellulose nanocrystals (CNCs) grafted with a random copolymer as the stabilizer. Firstly, poly(acrylonitrile--butyl acrylate) (poly(AN-BA)) was synthesized by Cu(0)-mediated CRP, which was further modified a click chemistry strategy to obtain poly(ethylene tetrazole--butyl acrylate) (poly(VT-BA)). Then, poly(VT-BA) was grafted onto the CNCs through a Mitsunobu reaction to obtain poly(VT-BA)--CNCs.

Removal of Cd(II) and Fe(III) from DMSO by silica gel supported PAMAM dendrimers: Equilibrium, thermodynamics, kinetics and mechanism.

A series of silica gel supported amino-terminated PAMAM dendrimers (SG-G1.0 - SG-G3.0) were used for the removal of Cd(II) and Fe(III) from dimethylsulfoxide (DMSO).

Synthesis of silica gel supported salicylaldehyde modified PAMAM dendrimers for the effective removal of Hg(II) from aqueous solution.

A series of silica gel supported salicylaldehyde modified PAMAM dendrimers (SiO2-G0-SA ∼ SiO2-G2.0-SA) were synthesized and their structures were characterized by FTIR, XRD, SEM, TGA, and porous structure analysis. The feasibility of these adsorbents for the removal of Hg(II) from aqueous solution was first described and the adsorption mechanism was proposed.

Adsorption of Pb(II) from aqueous solution by silica-gel supported hyperbranched polyamidoamine dendrimers.

The adsorption properties of silica-gel supported hyperbranched polyamidoamine dendrimers (SiO(2)-G0-SiO(2)-G4.0) have been investigated by batch method. The effect of pH of the solution, contact time, initial Pb(II) ion concentration, temperature and coexisting metal ions have been demonstrated.

Electronic structures of bis- and monothiophene complexes with Fe, Co, Ni: a density functional theory study.

A density functional theory study for the bis- and monothiophene complexes of Fe, Co, and Ni (MT2 and MT, T = thiophene, M = Fe, Co, Ni) was performed to understand their coordination geometries, bonding properties, vibration spectra and singlet excited state spectra. The typical metal coordination exists in the complexes. The Fe-thiophene coordination has the highest stability, with Ni-thiophene being the second highest, and Co-thiophene the lowest.

Comparison of synthesis of chelating resin silica-gel-supported diethylenetriamine and its removal properties for transition metal ions.

Four kinds of silica-gel (SG)-supported diethylenetriamine (DETA) chelating resins SG-DETA-1, SG-DETA-2, SG-DETA-3, and SG-DETA-4 were prepared by functionalization of silica-gel via so-called "heterogeneous-direct-amination" (hetero-DA), "homogeneous-direct-amination" (homo-DA), "heterogeneous end-group protection" (hetero-EGP), and "homogeneous end-group protection" (homo-EGP) routes, respectively. These functionalized reactions on silica-gel were confirmed through elemental analysis, infrared spectroscopy, X-ray diffractometry, porous analysis, and thermogravimetry. Element analysis revealed that the direct-amination routes and homogeneous condition were more beneficial than the corresponding end-group protection routes and heterogeneous condition to the syntheses of chelating resins with high N content.

Preparation and metal-binding behaviour of chitosan functionalized by ester- and amino-terminated hyperbranched polyamidoamine polymers.

A series of insoluble chitosan (CTS) derivatives were prepared by grafting ester- and amino-terminated dendrimer-like polyamidoamine (PAMAM) into CTS using a divergent method by repeating two processes: (1) Michael addition of methyl acrylate (MA) to surface amino groups, and (2) amidation of the resulting esters with ethylenediamine (EDA). Their structures were characterized by infrared spectra (IR) and wide-angle X-ray diffraction (WAXD). The adsorption capabilities of the products for Au(3+), Pd(2+), Pt(4+), Ag(+), Cu(2+), Zn(2+), Hg(2+), Ni(2+), and Cd(2+) were studied.