Hydrophobic‐Force‐Driven Removal of Organic Compounds from Water by Reduced Graphene Oxides Generated in Agarose Hydrogels

Hydrophobic reduced graphene oxides (rGOs) were generated in agarose hydrogel beads (AgarBs) by NaBH₄ reduction of graphene oxides (GOs) initially loaded in the AgarBs. The resulting rGO‐loaded AgarBs were able to effectively adsorb organic compounds in water as a result of the attractive hydrophobic force between the rGOs in the AgarBs and the organic compounds dissolved in aqueous media. The adsorption capacity of the rGOs was fairly high even toward reasonably water‐soluble organic compounds such as rhodamine B (321.7 mg g^?1) and aspirin (196.4 mg g^?1). Yet they exhibited salinity‐enhanced adsorption capacity and preferential adsorption of organic compounds with lower solubility in water. Such peculiar adsorption behavior highlights the exciting possibility for adopting an adsorption strategy, driven by hydrophobic forces, in practical wastewater treatment processes.     

Near‐Infrared Fluorescent Molecular Probe for Sensitive Imaging of Keloid

Early detection of skin diseases is imperative for their effective treatment. However, fluorescence molecular probes that allow this are rare. The first activatable near‐infrared (NIR) fluorescent molecular probe is reported for sensitive imaging of keloid cells, skin cells from abnormal scar fibrous lesions. As keloid cells have high expression levels of fibroblast activation protein‐alpha (FAPα), the probe (FNP1) is designed to have a caged NIR dye and a FAPα‐cleavable peptide substrate linked by a self‐immolative segment. FNP1 can quickly and specifically turn on its fluorescence at 710 nm by 45‐fold in the presence of FAPα, allowing it to effectively recognize keloid cells from normal skin cells. Integration of FNP1 with a simple microneedle‐assisted topical application enables sensitive detection of keloid cells in metabolically‐active human skin tissue with a theoretical limit of detection down to 20 000 cells.     

Towards chemical analysis of nanostructures in biofilms II: tip-enhanced Raman spectroscopy of alginates

This study examines the feasibility of using tip-enhanced Raman spectroscopy (TERS) for label-free chemical characterization of nanostructures in biological systems. For this purpose, a well-defined model system consisting of calcium alginate fibers is studied. In a companion paper, calcium alginate fibers and their network structures were shown to be a good model for the extracellular polysaccharides of biofilms at the nanoscale. TERS analysis of biological macromolecules, such as alginates, is complicated by heterogeneity in their sequence, molecular weight, and conformations, their small Raman cross-section, and the large number of functional groups, which can chemically interact with the silver surface of the tip and cause significant band shifts. Due to these effects, Raman frequencies in TERS spectra of biopolymers do not necessarily resemble band positions in the normal Raman spectrum of the bulk material, as is the case for less complex samples (e.g., dye molecules) studied so far. Additionally, analyte decomposition due to laser heating can have a significant influence, and carbon contamination signals can sometimes even overwhelm the weak analyte signals. Based on the investigation of alginates, strategies for spectra correction, choice of appropriate reference samples, and data interpretation are presented. With this approach, characteristic frequency ranges and specific marker bands can be found for biological macromolecules that can be employed for their identification in complex environments. Figure TERS spectrum of a calcium alginate fiber bundle     

Towards chemical analysis of nanostructures in biofilms I: imaging of biological nanostructures

Due to their direct influence on the stability of bacterial biofilms, a better insight into the nanoscopic spatial arrangement of the different extracellular polymeric substances (EPS), e.g., polysaccharides and proteins, is important for the improvement of biocides and for process optimization in wastewater treatment and biofiltration. Here, the first application of a combination of confocal laser-scanning microscopy (CLSM) and atomic force microscopy (AFM) to the investigation of river-water biofilms and related biopolymers is presented. AFM images collected at selected areas of CLS micrographs dramatically demonstrate the heterogeneity of biofilms at the nanometer scale and the need for a chemical imaging method with nanoscale resolution. The nanostructures (e.g., pili, flagella, hydrocolloids, and EPS) found in the extracellular matrix are classified according to shape and size, which is typically 50–150 nm in width and 1–10 nm in thickness, and sets the demands regarding spatial resolution of a potential chemical imaging method. Additionally, thin layers of the polysaccharide alginate were investigated. We demonstrate that calcium alginate is a good model for the EPS architecture at the nanometer scale, because of its similar network-like structure. Figure CLSM-AFM allows imaging of nanometer-sized extracellular structures     

Superparamagnetic iron oxide nanoparticles with photoswitchable fluorescence

The incorporation of superparamagnetic iron oxide nanoparticles with sulfur-oxidized diarylethene molecules resulted in a novel multifunctional nanosystem, in which the fluorescent performance and flocculation and dispersion are reversibly switched by light irradiation and external magnetic field, respectively.     

A new chromone, 11-hydroxy-sec-O-glucosylhamaudol from Ostericum koreanum

From the ethyl acetate fraction of the roots of Ostericum koreanum, a new chromone, 11-hydroxy-sec-O-glucosylhamaudol (1) along with the known compounds: four chromones, three coumarins, six phenolic compounds, and three quinic acids were isolated. These compounds were assessed for antioxidant activities in the DPPH radical and superoxide anion radical scavenging assay systems. Among isolates, 4-(2-hydroxy-vinyl)-benzene-1,2-diol (12) showed the most potent DPPH radical scavenging activity (IC(50)=4.80+/-0.62 mug/ml) and superoxide anion radical scavenging activity (IC(50)=11.05+/-0.83 microg/ml) in the xanthine/xanthine oxidase system. The antioxidant activities of 12 were comparable to those of quercetin and luteolin.     

Microstructure effect in the coupling reactions of polymeric organolithium compounds using chlorosilanes

The most important variable affecting the yield in the coupling reactions of polymeric organolithium compounds with chlorosilane compounds has been investigated through size-exclusion chromatographic (SEC) analysis. The coupling reaction of poly(styryl)lithium with dichlorodimethylsilane as a silane-coupling agent provided 44 wt % of the coupling yield. The coupling yield, depending on the chain end reactivity of active polymers, was not greatly affected. The addition of a Lewis base such as N,N,N′,N′-tetramethylethylenediamine (TMEDA) even after complete polymerization of the dienes in hydrocarbon seems to affect the coupling reaction, resulting in decreasing the yield. The 1,2- or 3,4-enchain contents in the polydiene backbones affected the reduction of the linking efficiency in the coupling of the poly(dienyl)lithiums with chlorosilanes as the linking agent. The linking yields of the active polymers including over 75 mol % of 1,2- or 3,4-enchainment on the polydiene segment were below 20 wt %. The linking yields exhibited a dependence not only on the steric requirement of the chain end, but also the microstructure of the polydiene segment. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1743–1753, 1998     

Hamilton cycles,avoiding prescribed arcs,in close-to-regular tournaments

The local irregularity of a digraph D is defined as i_l(D) = max {|d⁺ (x) − d⁻ (x)| : x ϵ V(D)}. Let T be a tournament, let Γ = {V₁, V₂, …, V_c} be a partition of V(T) such that |V₁| ≥ |V₂| ≥ … ≥ |V_c|, and let D be the multipartite tournament obtained by deleting all the arcs with both end points in the same set in Γ. We prove that, if |V(T)| ≥ max{2i_l(T) + 2|V₁| + 2|V₂| − 2, i_l(T) + 3|V₁| − 1}, then D is Hamiltonian. Furthermore, if T is regular (i.e., i_l(T) = 0), then we state slightly better lower bounds for |V(T)| such that we still can guarantee that D is Hamiltonian. Finally, we show that our results are best possible. © 1999 John Wiley & Sons, Inc. J Graph Theory 32: 123–136, 1999     

Simulation of three‐dimensional bubbles using desingularized boundary integral method

A very simple model based on the three‐dimensional desingularized boundary integral method is applied to study the evolution of bubble(s) with or without the presence of solid structures. The choice of the desingularization parameters, which is crucial to the success of the method, is studied in the context of bubble dynamics. With the proper choice of parameters, the new model is far more efficient than previous models with virtually the same level of accuracy being achieved. This is largely attributed to the simplicity of the desingularization method. Furthermore, the new model offers a simple and attractive way for mesh refinement. Although it has limitations in the sense that, with this model the time stepping tends to slow down as two surfaces approach each other, this can be easily rectified by switching over to a direct method so that the two surfaces can be drawn closer as required in the context of jet impact. After this the new model can be reinstated to treat the complicated doubly connected geometry involving toroidal bubbles that would otherwise be very difficult to deal with. Copyright © 1999 John Wiley & Sons, Ltd.