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.

Graphite felt is a felt-like porous material made of high-temperature carbonized polymers. It is widely used in electrode materials because of its good temperature resistance, corrosion resistance, large surface area and excellent electrical conductivity. In this paper, the surface functional group modification is of graphite felt electrodes (mainly nitrogen doping modification, nitrogen–sulfur or nitrogen–boron co-doping modification) and surface catalytic modification (metal/ion surface modification and metal oxide surface modification as Main). There are two main methods and research progresses to improve the performance of graphite felt electrodes, and the comprehensive performance of surface functional group-modified graphite felt electrodes and surface catalytically modified graphite felt electrodes are compared respectively. The results show that both surface functional group modification and surface catalytic modification can improve the comprehensive performance of graphite felt electrodes. In this paper, the future development direction of graphite felt activation modification is also prospected.

The main objective of the research was to deposit thin films of silver on a graphite carbon paste in a phosphate buffer medium using an electrochemical method. To construct a nitrofurazone detection sensor that is highly sensitive. Different manufacturing parameters, such as electrodeposition potential, pH effect, potential scan rate effect, and number of scan cycles, were examined in this section. The parameters were optimized to improve the deposited silver layers various electrocatalytic characteristics. The Nitrofurazone reduction process is diffusion controlled, as seen by the linear variation of Epc with log(v). The constructed Ag-NPs@CPE electrod has excellent electrical characteristics a large active surface area and low background with extremely high electrical conductivity, according to structural and electrochemical characterizations such as Scanning electron microscopy, X-ray diffraction (XRD) and cyclic voltammetry. The constructed sensor has a very remarkable analytical performance for nitrofurazone molecule identification, with a very low detection limit of about 10– 8 M. The detection of nitrofurazone using our Ag-NPs@CPE sensors in real samples contaminated with the antibiotic nitrofurazone, such as tap water and urine. In the selected sample, the electroanalytical findings reveal a very satisfactory recovery rate of more than 94 percent.

This work describes the facile synthesis of silver nanoparticle-decorated zinc oxide nanocomposite through a simple glycol reduction method. The silver nanoparticle-decorated zinc oxide nanocomposite-based pencil graphite electrode has been validated as a perceptive electrochemical sensing podium towards nitrite. The morphology of the prepared nanocomposite has been characterized via specific spectroscopic and electrochemical techniques. The sensor exhibits a notable enhancement in the cyclic voltammetric response to nitrite oxidation at an ideal peak potential of 0.76 V in pH 6.0 acetate buffer. Under optimum conditions of nitrite directly expanded with their concentration in the range from 30 to 1400 μM with a detection limit of 14 μM.

신축성 전극을 다양한 소재와과 방식을 통해 제조되고 있으며 많은 기계적 특성 분석이 연구되고 있다. 은, 구리, 금, 나노와이어 등 다양한 금속이나 CNT, graphene, 플러렌 등을 기반으로 연구되고 있으며 대부분 높은 전도성과 신축특성을 요구하는 어플리케이션에 사용되지만 고가라는 단점이 있다. 본 연구에서는 저비용 소재와 공정으로 높은 신축특성과 반복 특성을 보유한 신축성 전극을 개발하였다. 값싼 전도성 탄소 와 흑연을 혼합하여 페이스트를 개발하였고 개발된 페이스트를 메탈마스크 인쇄 공정을 통해 TPU기판 위에 인쇄하였고 120℃에서 2시간 경화를 진행하였다. 이렇게 개발된 전극을 인장 시험과 인장 반복 시험을 통해 특성을 증명하였고 향후 어플리케이션 적용 가능여부를 확인하기 위해 무릎에 임시로 고정 후 간이 시험을 진행한 결과 20회 반복하는 동안 일정한 저항 변화를 보여줬다.

The natural graphite particles A and heat-treated graphite particles B at 1800 ℃ after pitch-coating were used as the anode base materials for lithium ion secondary battery. In order to improve the performance of anode materials, the base anode materials were treated with various acids. With the acid treatments of 62% HNO3 and 95% H2SO4 aqueous solution, the specific surface area and electrical conductivity of base anode materials were increased, and the initial charge-discharge capacity and cycle performance were improved due to the elimination of structural defects.

스킨로션에 함유된 루틴을 정량하기 위하여 사각파형 전압전류법에서 흑연을 작업 전극으로 사용하여 연구하였다. 루틴을 정량하기 위한 최적 분석 조건을 찾았고 이 조건에서 1.00 ~ 8.00 µg/mL의 농도에 대한 루틴의 검량선을 나타내었다. 0.10 µg/mL의 루틴 농도에서 15번 반복 측정한 상대 표준편차는 0.08이였으며, 최소 분석 검출 한계는 0.01 µg/mL로 나타났다. 이 결과들을 바탕으로 화장품에 함유되어 있는 활성성분을 정량하는데 사용가능할 것으로 사료된다.

For the RhB removal from the wastewater, electrochemical method was adapted to this study. Three dimensionally stable anode (Pt, Ir and Ru) and graphite and Ru cathode were used. In order to identify decolorization, the effects of electrode, current density, electrolyte and air flow rate were investigated. The effects of electrode material, current, electrolyte concentration and air flow rate were investigated on the decolorization of RhB. Electro-Fenton's reaction was evaluated by added Fe2+ and H2O2 generated by the graphite cathode. Performance for RhB decolorization of the four electrode systems lay in: Ru-graphite > Ru-Ru > Ir-graphite > Pt-graphite. A complete color removal was obtained for RhB (30 mg/L) at the end of 30 min of electrolysis under optimum operations of 2 g/L NaCl concentration and 2 A current. Fe2+ addition increased initial reaction and decreased final RhB concentration. However the effect was not high.