The nanostructured dysprosium oxide ( Dy2O3) was synthesized by the co-precipitation method and incorporated with graphitic carbon nitride (g-C3N4) using the ultrasonication method. The resultant product is denoted as Dy2O3/ g-C3N4 nanocomposite which was further used for electrochemical sensing of riboflavin (RF). The physicochemical properties of Dy2O3/ g-C3N4 nanocomposite were examined using several characterization techniques. The obtained results exhibit the nanocomposite formation with the preferred elemental compositions, functional groups, crystalline phase and desired surface morphology. The electrocatalytic performance of Dy2O3/ g-C3N4 nanocomposite was scrutinized with a glassy carbon electrode (GCE) via differential pulse voltammetry (DPV) and cyclic voltammetry (CV) techniques with the conventional three-electrode system. The modified electrode distributes more active surface area suggesting high electrocatalytic activity for the RF detection with two linear ranges (0.001–40 μM and 40–150 μM), a low detection limit of 48 nM and sound sensitivity (2.5261 μA μM−1 cm− 2). Further, the designed sensor possesses high selectivity, excellent stability, repeatability and reproducibility. Finally, the fabricated sensor was successfully estimated for the detection of RF in actual food sample analysis using honey and milk with better recovery.

The dyeing process is a very important unit operation in the leather and textile industries; it produces significant amounts of waste effluent containing dyes and poses a substantial threat to the environment. Therefore, degradation of the industrial dye-waste liquid is necessary before its release into the environment. The current is focusing on the reduction of pollutant loads in industrial wastewater through remediating azo and thiazine dyes (synthetic solutions of textile dye consortium). The current research work is focused on the degradation of dye consortium through photo-electro-Fenton (PEF) processes via using dimensionally stable anode (Ti) and graphite cathode. The ideal conditions, which included a pH of 3, 0.1 (g/L) of textile dye consortium, 0.03 (g/L) of iron, 0.2 (g/L) of H2O2, and a 0.3 mAcm-2 of current density, were achieved to the removal of dye consortium over 40 min. The highest dye removal rate was discovered to be 96%. The transition of azo linkages into N2 or NH3 was confirmed by Fourier transforms infra-red spectroscopic analysis. PEF process reduced the 92% of chemical oxygen demand (COD) of textile dye consortium solution, and it meets the kinetics study of the pseudo-first-order. The degradation of dye through the PEF process was evaluated by using the cyclic voltammetric method. The toxicity tests showed that with the treated dye solution, seedlings grew well.

In this work, a nanocomposite containing gold (Au) nanofibers decorated iron-metal–organic framework (Fe-MOF) was successfully synthesized for electrochemical detection of acetaminophen (AAP). The as-synthesized Au@Fe-MOF nanocomposite was confirmed by various characterization techniques. Morphological analysis showed that the Au nanofibers with an average size of less than 10 nm were dispersed on the Fe-MOF. Cyclic voltammetric analysis showed that the Au@Fe-MOF nanocomposite showed well-defined redox peaks with higher current than that of GCE and Fe-MOF. The Au@Fe-MOF/ GCE exhibited a linear range, sensitivity, and detection limit of 0.5–18 μM, 4.95 μM/μA/cm2, and 0.12 μM, respectively. The Au@Fe-MOF/GCE showed a very low response for the interference materials. The real sample analysis revealed that the Au@Fe-MOF/GCE showed good recovery towards the AAP in urine and paracetamol. Therefore, the developed sensor can be used for quality control of AAP.

Herein, a new and generic strategy has been proposed to introduce uniformly distributed graphitic carbon into the nanostructured metal oxide. A facile and generic synthetic protocol has been proposed to introduce uniformly distributed conducting graphitic carbon into the Co3O4 nanoparticles ( Co3O4 NPs@graphitic carbon). The prepared Co3O4 NPs@graphitic carbon has been drop casted onto the portable screen-printed electrode (SPE) to realize its potential application in the individual and simultaneous quantification of toxic Pb(II) and Cd(II) ions present in aqueous solution. The proposed Co3O4 NPs@graphitic carbon-based electrochemical sensor exhibits a wide linear range from 0 to 120 ppb with limit of detection of 3.2 and 3.5 ppb towards the simultaneous detection of Pb(II) and Cd(II), which falls well below threshold limit prescribed by WHO.

Activated non-graphitizable hard carbon using orange peel with mesoporous structure has been prepared by pyrolyzation at 700, 800, 900 °C using chemical activation method. The activated orange peel-derived hard carbon has been characterized for its mesoporous and disordered structure. TG-DSC gives the information for the changes about sample composition and thermal stability of the materials. Increasing the carbonization temperature for orange peel precursor using NaOH as activating agent, elevates the pore diameter, which thereby facilitating the insertion of Na+. Raman and X-ray diffraction confirms the presence of disordered carbon. The surface morphology of the material was analyzed by scanning eletron microsope and nitrogen ( N2) adsorption and desorption analysis give the morphology, mesopore size (3.374, 3.39 and 4 nm) and surace area (60.164, 58.99 and 54.327 m2/g) of the orange peel-derived hard carbon. Hence, this work strongly evidences that the biomass-derived hard carbon with good porosity and paves way of superior electrochemical performance for emerging sodium ion batteries.

Abstract Activated carbon from the shell of the cashew of Para (SCP) was produced by chemical activation with ZnCl using the ratio of SCP: ZnCl2 1.0:1.5 at 700 °C. The prepared activated carbon (SCP700) was used for the removal of two emerging contaminants, 4-bromophenol (4-BrPhOH) and 4-chloroaniline (4-ClPhNH2) that are primarily employed in the industry. Different analytical techniques were used to characterize the activated carbon. From the N2 adsorption–desorption isotherms were obtained the specific surface area of 1520 m2 g− 1 and total pore volume of 0.492 cm3 g−1. The functional groups were identified by the FTIR technique and quantified by modified Boehm titration. The results revealed the bearing of several functional groups on the SCP700 surface, which may utterly influence the removal of the emerging contaminants. The equilibrium experiments showed that the maximum uptaken capacities (Qmax) achieved at 45 °C were 488.2 (4-BrPhOH) and 552.5 mg g−1 (4-ClPhNH2). The thermodynamic parameters demonstrated that the processes of 4-BrPhOH and 4-ClPhNH2 adsorption are exothermic, spontaneous, energetically suitable, and the magnitude of ΔH° is compatible with physisorption. The mechanism of the adsorption of the emerging contaminants onto the carbon surface is dominated by microporous filling, hydrogen bonds, π-stacking interactions, and other Van der Waals interactions. The use of activated carbon for the treatment of industrial synthetic wastewater with several inorganic and organic molecules commonly found in industrial effluents showed a very high percentage of uptaking (up to 98.64%).

본 리뷰 논문은 식품 산업에서 나노 기술의 활용에 관한 보고이다. 식품 병원균에 대한 항균 활성을 갖는 생리 활성 성분은 식품 보존시 효율성을 향상시키고 보존성을 증진시키기 위해 나노입자(NPs)로 캡슐화된다. 그러나, 이러한 NPs는 인간에게 생체 적합성과 무독성을 지녀야 된다. 식품 보존분야의 발전은 일부 산업 분야에서 식품 포장용 NPs의 개발을 가져왔다. 식품 산업 분야에서 가장 일반적으로 사용되는 NPs 그룹은 금속 산화물이다. 산화 아연과 이산화 티타늄 같은 금속 산화물 NPs는 식품 재료에 서 항균 활성을 나타내기 때문에, NPs는 강화된 기능적 특성으로 식품 보존에 사용될 수 있다. 식품 영양과 관능적 특성과 관련된 나노 기술의 적용은 나노 기반 식품 제조 및 보존에 관한 안전규제를 중심으로 간략하게 정리하였다.

In late 1950’s, the beginning of container revolution has started a new paradigm shift in maritime industry worldwide. This new paradigm has become a major reason for seaport systems to prepare their physical capacity, space availability, multi-modalism, transport connectivity via regionalisation. However, in early 2010’s the introduction of industrial revolution 4.0 (IR4.0) which starts the era of immersive digitalization proved that seaport systems need to be prepared to face pattern of unstable magnitudes in dynamic maritime trade. Therefore, this paper analyses key components required for Malaysian seaport system to be aligned with the key requirements in IR4.0. By employing document analysis, this research analyses the challenges faced by Malaysian seaport system as well as suggests strategies to muddle through the key requirements of IR4.0. The findings from this research indicate that Malaysian seaport system need to be improved by enforcing skill-based education system, flexibility in labour structure, development in skill and competence level as well as improvement in infrastructure suitability. The findings from this research also reflect significant strategies to improve seaport system in the era of IR4.0 including enhancing requirements for intermodal terminals, improving preparation for seaport alliances, developing mechanism for interoperability, improving utilisation of intra and interregional economic development as well as scrutinising safety and security.

Research on the useful mushroom was done at Aurora Memorial National Park (AMNP). The Park is situated in Central Luzon Region with a total land area of 5,676 hectares. AMNP has no distinct wet and dry season thus provides a favorable climate, which promotes the growth of useful mushrooms. The photo-documentation and collections were performed to assess diversity. Five Transect Lines (TL) were laid out in five areas, with 20m x 30m quadrat and interval of 100 meters between quadrats. The study resulted in the identification of 36 families, 53 genera, and 104 species of which 97 are basidiomycetes and 6 are ascomycetes. Simpson’s and Shannon diversity indexes resulted in 0.7254 and 1.4295, respectively. In both indexes, useful mushrooms at AMNP showed moderately diverse. While the evenness revealed 0.1565 indicating low species evenness in each TL. Among the significant findings revealed two new possible new species of Microporus and Cymatoderma.