Faming Gao

Sorption enhancement of lead ions from water by surface charged polystyrene-supported nano-zirconium oxide composites.

A novel hybrid nanomaterial was fabricated by encapsulating ZrO2 nanoparticles into spherical polystyrene beads (MPS) covalently bound with charged sulfonate groups (-SO3(-)). The resultant adsorbent, Zr-MPS, exhibited more preferential sorption toward Pb(II) than the simple equivalent mixture of MPS and ZrO2. Such observation might be ascribed to the presence of sulfonate groups of the polymeric host, which could enhance nano-ZrO2 dispersion and Pb(II) diffusion kinetics. To further elucidate the role of surface functional groups, we encapsulated nano-ZrO2 onto another two macroporous polystyrene with different surface groups (i.e., -N(CH3)3(+)/-CH2Cl, respectively) and a conventional activated carbon. The three obtained nanocomposites were denoted as Zr-MPN, Zr-MPC, and Zr-GAC. The presence of -SO3(-) and -N(CH3)3(+) was more favorable for nano-ZrO2 dispersion than the neutral -CH2Cl, resulting in the sequence of sorption capacities as Zr-MPS > Zr-MPN > Zr-GAC > Zr-MPC. Column Pb(II) sorption by the four nanocomposites further demonstrated the excellent Pb(II) retention by Zr-MPS. Comparatively, Zr-MPN of well-dispersed nano-ZrO2 and high sorption capacities showed much faster breakthrough for Pb(II) sequestration than Zr-MPS, because the electrostatic repulsion of surface quaternary ammonium group of MPN and Pb(II) ion would result in a poor sorption kinetics. This study suggests that charged groups in the host resins improve the dispersion of embedded nanoparticles and enhance the reactivity and capacity for sorption of metal ions. Suitably charged functional groups in the hosts are crucial in the fabrication of efficient nanocomposites for the decontamination of water from toxic metals and other charged pollutants.

Facile and Scalable Preparation of Graphene Oxide-Based Magnetic Hybrids for Fast and Highly Efficient Removal of Organic Dyes

This study reports the facile preparation and the dye removal efficiency of nanohybrids composed of graphene oxide (GO) and Fe3O4 nanoparticles with various geometrical structures. In comparison to previously reported GO/Fe3O4 composites prepared through the one-pot, in situ deposition of Fe3O4 nanoparticles, the GO/Fe3O4 nanohybrids reported here were obtained by taking advantage of the physical affinities between sulfonated GO and Fe3O4 nanoparticles, which allows tuning the dimensions and geometries of Fe3O4 nanoparticles in order to decrease their contact area with GO, while still maintaining the magnetic properties of the nanohybrids for easy separation and adsorbent recycling. Both the as-prepared and regenerated nanohybrids demonstrate a nearly 100% removal rate for methylene blue and an impressively high removal rate for Rhodamine B. This study provides new insights into the facile and controllable industrial scale fabrication of safe and highly efficient GO-based adsorbents for dye or other organic pollutants in a wide range of environmental-related applications.

Self-assembly, interfacial nanostructure, and supramolecular chirality of the Langmuir-Blodgett films of some schiff base derivatives without alkyl chain

A special naphthyl-containing Schiff base derivative, N, N′-bis(2-hydroxy-1-naphthylidene)-1,2-phenylenediamine, was synthesized, and its coordination with various metal ions in situ at the air/water interface has been investigated. Although the ligand contains no alkyl chain, it can be spread on water surface. When metal ions existed in the subphase, an interfacial coordination between the ligand and different metal ions occurred in the spreading film, while different Nanostructures were fabricated in the monolayers. Interestingly to note that among various metal ions, only the in situ coordination-induced Cu(II)-complex film showed supramolecular chirality, although the multilayer films from the ligand or preformed complex are achiral. The chirality of the in situ Cu(II)-coordinated Langmuir film was developed due to the special distorted coordination reaction and the spatial limitation at the air/water interface. A possible organization mechanism at the air/water interface was suggested.

Self-assembly of organogels via new luminol imide derivatives: diverse nanostructures and substituent chain effect

Luminol is considered as an efficient sycpstem in electrochemiluminescence (ECL) measurements for the detection of hydrogen peroxide. In this paper, new luminol imide derivatives with different alkyl substituent chains were designed and synthesized. Their gelation behaviors in 26 solvents were tested as novel low molecular mass organic gelators. It was shown that the length and number of alkyl substituent chains linked to a benzene ring in gelators played a crucial role in the gelation behavior of all compounds in various organic solvents. Longer alkyl chains in molecular skeletons in present gelators are favorable for the gelation of organic solvents. Scanning electron microscope and atomic force microscope observations revealed that the gelator molecules self-assemble into different micro/nanoscale aggregates from a dot, flower, belt, rod, and lamella to wrinkle with change of solvents. Spectral studies indicated that there existed different H-bond formations and hydrophobic forces, depending on the alkyl substituent chains in molecular skeletons. The present work may give some insight to the design and characteristic of new versatile soft materials and potential ECL biosensors with special molecular structures.

Rationally designed porous polystyrene encapsulated zirconium phosphate nanocomposite for highly efficient fluoride uptake in waters

Fluoride pollution in waters has engulfed worldwide regions and an excess of fluoride intake always causes skeletal fluorosis. Herein, a novel hybrid nanomaterial ZrP-MPN was fabricated for fluoride retention by encapsulating nano-ZrP onto macroporous polystyrene materials modified with quaternary ammonium groups. The as-obtained materials exhibited favorable removal of fluoride ions from aqueous solution in presence of common anions (SO42−/NO3−/Cl−) at high contents. Moreover outstanding sorption properties were also detected by involving series of commercial adsorbents (AA/magnetite/GFH/manganese sands) as references. Such satisfactory performances might be ascribed to the structural design of nanocomposite. (1) the CH2N+(CH3)3Cl groups enhances sorption diffusion and preconcentration in sorbent phase theoretically based on Donnan membrane principle; (2) the embedded ZrP nanoparticles also devotes to the efficient adsorption capacities due to its size-dependent specific properties. Additionally, the exhausted ZrP-MPN could be regenerated readily by alkaline solution. Thus, ZrP-MPN was a promising material for fluoride retention in waters.

Supramolecular Gel and Nanostructures of Bolaform and Trigonal Cholesteryl Derivatives with Different Aromatic Spacers

New bolaform and trigonal cholesteryl amide derivatives with different aromatic spacers were designed and prepared. Their gelation behaviors in 20 solvents were tested as novel low-molecular-mass organic gelators (LMOGs). It was shown that the size of the spacer connecting cholesteryl residues in gelators plays a crucial role in the gelation behavior of the compounds. While the trigonal compound gels 3 of the 20 solvents tested at a concentration more than 3.0%, the bolaform compound gels 2 of the solvents tested at a concentration more than 2.0%, respectively. SEM and AFM observations reveal that the size of the spacers and the identity of the solvents are the main factors affecting the structures of the aggregates in the gels. Experimentally, a clear spacer effect on the microstructures of the gels was observed. As example, the aggregates of trigonal compound in 1,4-dioxane, aniline, or nitrobenzene adopt structures of lamella, rod, or belt, respectively. The present work may give some insight to design and character new organogelators with special molecular structures.

Regulation of substituent groups on morphologies and self-assembly of organogels based on some azobenzene imide derivatives

In this paper, new azobenzene imide derivatives with different substituent groups were designed and synthesized. Their gelation behaviors in 21 solvents were tested as novel low-molecular-mass organic gelators. It was shown that the alkyl substituent chains and headgroups of azobenzene residues in gelators played a crucial role in the gelation behavior of all compounds in various organic solvents. More alkyl chains in molecular skeletons in present gelators are favorable for the gelation of organic solvents. Scanning electron microscopy and atomic force microscopy observations revealed that the gelator molecules self-assemble into different aggregates, from wrinkle, lamella, and belt to fiber with the change of solvents. Spectral studies indicated that there existed different H-bond formations between amide groups and conformations of methyl chains. The present work may give some insight to the design and character of new organogelators and soft materials with special molecular structures.

Self-Assembly and Headgroup Effect in Nanostructured Organogels via Cationic Amphiphile-Graphene Oxide Composites

Self-assembly of hierarchical graphene oxide (GO)-based nanomaterials with novel functions has received a great deal of attentions. In this study, nanostructured organogels based on cationic amphiphile-GO composites were prepared. The gelation behaviors of amphiphile-GO composites in organic solvents can be regulated by changing the headgroups of amphiphiles. Ammonium substituted headgroup in molecular structures in present self-assembled composites is more favorable for the gelation in comparison to pyridinium headgroup. A possible mechanism for headgroup effects on self-assembly and as-prepared nanostructures is proposed. It is believed that the present amphiphile-GO self-assembled system will provide an alternative platform for the design of new GO nanomaterials and soft matters.

Spacer effect on nanostructures and self-assembly in organogels via some bolaform cholesteryl imide derivatives with different spacers

In this paper, new bolaform cholesteryl imide derivatives with different spacers were designed and synthesized. Their gelation behaviors in 23 solvents were investigated, and some of them were found to be low molecular mass organic gelators. The experimental results indicated that these as-formed organogels can be regulated by changing the flexible/rigid segments in spacers and organic solvents. Suitable combination of flexible/rigid segments in molecular spacers in the present cholesteryl gelators is favorable for the gelation of organic solvents. Scanning electron microscopy and atomic force microscopy observations revealed that the gelator molecules self-assemble into different aggregates, from wrinkle and belt to fiber with the change of spacers and solvents. Spectral studies indicated that there existed different H-bond formations between imide groups and assembly modes, depending on the substituent spacers in molecular skeletons. The present work may give some insight into the design and character of new organogelators and soft materials with special molecular structures.

Nanostructures and self-assembly of organogels via benzimidazole/benzothiazole imide derivatives with different alkyl substituent chains

New benzimidazole/benzothiazole imide derivatives with different alkyl substituent chains were designed and synthesized. Their gelation behaviors in 22 solvents were tested as novel low-molecular-mass organic gelators. The test showed that the alkyl substituent chains and headgroups of benzimidazole/benzothiazole residues in gelators played a crucial role in the gelation behavior of all compounds in various organic solvents. More alkyl chains in molecular skeletons in present gelators are favorable for the gelation of organic solvents. SEM and AFM observations revealed that the gelator molecules self-assemble into different aggregates from wrinkle, lamella and belt to dot with change of solvents. Spectral studies indicated that there existed different H-bond formation between imide groups and hydrophobic force of alkyl substituent chains in molecular skeletons. The present work may give some insights into design and character of new organogelators and soft materials with special molecular structures.