Antioxidant activities of phlorotannins purified from Ecklonia cava on free radical scavenging using ESR and H2O2-mediated DNA damage

The potential antioxidant activities of three phlorotannins (phloroglucinol, eckol and dieckol) purified from Ecklonia cava collected in Jeju Island were investigated to evaluate their potential value as the natural products for foods or cosmetic application. In this study, antioxidant activities were measured by electron spin resonance spectrometry (ESR) technique for scavenging effects of free radicals such as 1,1-diphenyl-2-picrylhydrazyl (DPPH), alkyl, hydroxyl (HO^•) and superoxide anion radical (O₂ ^•−) and by comet assay for protecting effects against H₂O₂-mediated DNA damage. The results show that all the phlorotannins have the potential DPPH, alkyl, hydroxyl and superoxide radical scavenging activities. Especially, eckol samples scavenged around 93% of DPPH at 0.25, 0.5, 1 mg/mL of concentrations and were higher than the other phlorotannins, such as phloroglucinol and dieckol samples. Also, protecting effects of the phlorotannins against H₂O₂-mediated DNA damage increased with increased concentrations of the samples in the L5178 mouse T-cell lymphoma cell lines (L5178Y-R). In conclusion, these results suggest that the three phlorotannins purified from E. cava have the potential inhibitory effect on H₂O₂-mediated DNA damage and harmful free radicals and can be used as antioxidants in cosmetic, foods and drug industry.     

Hydrothermal synthesis of PtRu nanoparticles supported on graphene sheets for methanol oxidation in direct methanol fuel cell

Platinum–ruthenium (PtRu) nanoparticles are dispersed on graphene nanosheets and multi-walled carbon nanotubes (MWCNTs) via a hydrothermal method. Transmission electron microsocopy (TEM) observation shows the uniformly dispersed nanoparticles and the average nanoparticle size has been calculated. The electrochemical measurements demonstrate that the Pt–Ru/graphene catalyst exhibits about two times higher mass activity and better tolerance to poisoning species in methanol electro-oxidation than the Pt–Ru/MWCNTs catalyst. This study indicates that the PtRu anodic catalyst synthesized by hydrothermal method can be applied for direct methanol fuel cells (DMFC).     

Sustainability decision support system based on collaborative control theory

Industries nowadays have more insight into corporate environmental, social and economic sustainability than ever before. Sustainability issues in various industries are all about choices – finding ways to be more strategic and reducing waste and energy, while benefiting the bottom line. Because of the complexity of sustainability decisions and strategies, these insights call for applying advanced control techniques. In this article we review the concepts of sustainability and its practical issues, specifically focusing on the issues of supply networks. Sustainability issues are usually complex because beyond their inherent challenges, there are conflicts among stakeholders within organizations and between organizations; hence, more useful methods are required for effective solutions. We consider Decision Support Systems (DSSs) to help optimize solutions related with sustainability issues, and review their concepts and usefulness based on previous work. We also suggest strategies applying the Collaborative Control Theory (CCT) principles to augment DSS by a new Sustainability – Decision Support Protocol (S-DSP) in order to overcome certain weaknesses. To model and illustrate the benefit of S-DSP as a control protocol, two practical supply delivery/production problems are analyzed. The results highlight how better collaborative solutions can be achieved to maximize the sustainability of supply networks. It is envisioned that sustainability decision support by such cyber-supported collaboration protocols will contribute to overcome the emerging challenges of sustainability planning and control.     

Development of a PCR assay for the detection of nifH and nifD genes in indigenous photosynthetic bacteria

Molybdenum (Mo) nitrogenases consist of two components: dinitrogenase reductase (encoded by nifH) and the dinitrogenase or MoFe protein (encoded by nifDK). Nitrogenase enzyme of photosynthetic bacteria is responsible for hydrogen production. Therefore, primers were designed for the nitrogenase gene only. In this study, two primers (ND and NH) were designed after comparative genomic analysis of nifH and nifD gene sequences from public databases. The designed primers were used for the amplification of nifH and nifD genes to detect nitrogenase genes in photosynthetic bacteria. Initial detection was done using a monoplex Polymerase Chain Reactions (PCRs) followed by optimization of the PCR protocols. Subsequently, a duplex PCR was designed for amplification and detection of nifH and nifD genes in indigenous photosynthetic bacteria. Evaluation of the duplex PCR on six samples isolated from Palm Oil Mill Effluent (POME) showed that only four isolates contained both the nifH and nifD genes, indicating that these isolates were potential hydrogen-producing bacteria. PCR detection provides a rapid and efficient pre-identification of potential photosynthetic bacterial hydrogen producers.     

Synthesis of two dimensional carbon sheets from adamantane

Graphene-like carbon sheets were synthesized from adamantane in the solution phase at ambient temperature. Adamantane, C₁₀H₁₆, has a tetracyclic ring structure with four cyclohexanes in chair conformation. The two dimensional carbon structures were obtained by introducing ferrocene as the catalyst precursor and adamantane as the carbon source under sonication, proving that cyclohexane structures in adamantane can serve as a building block for graphene formation. The synthesized carbon sheets were characterized and confirmed by X-ray diffraction, high-resolution electron microscopy and atomic force microscopy.     

Synthesis of monodisperse nickel‐coated polymer particles by electroless plating method utilizing functional polymeric ligands

In the electroless plating process, to omit a sensitizing process with SnCl₂, we utilized amino‐functional groups on polymer particles. At first, highly monodisperse functional polymer particles could be prepared by a two‐step seeded polymerization of styrene, divinylbenzene, and glycidyl methacrylate. Then, surface epoxy‐functional groups were converted to amino‐functional groups by treating the particles with a diamine. By using these surface amino functionalities, we tried to prepare uniformly metal‐coated monodisperse polymer particles by electroless plating method. The constituents of an electroless nickel solution bath are nickel salt, a reducing agent, suitable complexing agents, and stabilizers. And the metal thickness was simply controlled by changing the loading amount of substrate polymer particles. Morphological observation of nickel‐plated polymer particles was conducted by using optical microscopy, scanning electron microscopy, and transmission electron microscopy. The structural composition of plated nickel was also investigated. Most of all, the function and the efficiency of the amino‐functional group of polymer particles as a polymeric ligand for metal binding was elucidated. From all observations, it was evident that in the electroless metal plating process without any sensitization step, the deposition of metal clusters on substrate particles is largely dependent upon the particle surface functionality. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3801–3808, 2006     

Experimental study on forced convective boiling heat transfer of pure refrigerants and refrigerant mixtures in a horizontal tube

Convective boiling heat transfer coefficients of pure refrigerants (R22, R32, R134A, R290, and R600a) and refrigerant mixtures (R32/R134a, R290/R600a, and R32/R125) are measured experimentally and compared with Gungor and Winterton correlation. The test section is made of a seamless stainless steel tube with an inner diameter of 7.7 mm and is uniformly heated by applying electric current directly to the tube. The exit temperature of the test section was kept at 12°C ± 0.5°C for all refrigerants in this study. Heat fluxes are varied from 10 to 30 kW m⁻² and mass fluxes are set to the discrete values in the range of 424–742 kg m⁻² s⁻¹ for R22, R32, R134a, R32/R134a, and R32/R125; 265–583 kg m⁻² s⁻¹ for R290, R600a, and R290/R600a. Heat transfer coefficients depend strongly on heat flux at a low quality region and become independent as quality increases. The Gungor and Winterton correlation for pure substances and the Thome-Shakil modification of this correlation for refrigerant mixtures overpredicts the heat transfer coefficients measured in this study.     

Enhanced absorptive characteristics of metal nanoparticle-coated silicon nanowires for solar cell applications

The optical properties of metal nanoparticle (NP)-coated silicon nanowires (Si NWs) are theoretically investigated using COMSOL Multiphysics commercial software. A geometrical array of periodic Si NWs coated with metal NPs is proposed. The simulation demonstrates that light absorption could be enhanced significantly in a long wavelength region of the solar spectrum, based upon the localized surface plasmons generated around metal NPs. Various metal NPs, such as Au, Ag, and Al, are all found to increase their light absorption while in contact with Si NWs, in which the Au NPs show the best result in light enhancement. This theoretical work might prove useful in providing a fundamental understanding toward improving further the efficiency of Si wired solar cells.     

Comparative study on the properties of amorphous carbon layers deposited from 1-hexene and propylene for dry etch hard mask application in semiconductor device manufacturing

Amorphous carbon layers (ACLs) were prepared by plasma enhanced chemical vapor deposition (PECVD) from 1-hexene (C₆H₁₂) and propylene (C₃H₆) as a carbon source at different temperatures for dry etch hard mask of semiconductor devices manufacturing process. The deposition rate of ACL deposited at 550 °C from C₆H₁₂ and C₃H₆ was 5050 Å/min and 6360 Å/min. Although the deposition rate of ACL deposited from C₆H₆ was lower than that from C₃H₆, normalized deposition rate of ACL deposited from C₆H₁₂ was 1.64 times higher than that from C₃H₆. The relative amount of hydrocarbon contents measured by FTIR (Fourier transformation infrared) and TDS (thermal desorption spectroscopy) was decreased with the increase of deposition temperature. Raman results showed that the numbers and size of graphite cluster of ACLs deposited from each source were increased with the increase of deposition temperature. The extinction coefficient of ACL deposited at 550 °C from C₆H₁₂ was 0.51 and that from C₃H₆ was 0.48. The density of ACL deposited at 550 °C from C₆H₁₂ was 1.48 g/cm³ and that from C₃H₆ was 1.45 g/cm³. The dry etching rate of ACL deposited at 550 °C from C₆H₁₂ was 1770 Å/min and that from C₃H₆ was 1840 Å/min. The deposition rate, dry etch rate and the amount of hydrocarbon contents of ACLs deposited from each carbon source were decreased with the increase of deposition temperature but extinction coefficient and density were increased with the increase of deposition temperature. We concluded that the variation behavior of the deposition characteristics and film properties of ACLs from C₆H₁₂ with the increase of deposition temperature was the same as those of ACLs from C₃H₆. The high density and low dry etch rate of ACL from C₆H₁₂ can be explained by less hydrocarbon incorporation during deposition and these properties are more favorable for the dry etch hard mask application in semiconductor device fabrication.