We have intended and preparation of hierarchically absorbent materials were covered with a NiMn2O4 and acts as a catalyst for azo dye degradation. The polyaromatic-based (PA) absorbent compounds were initially constructed by bromomethylated aromatic hydrocarbons which undergo self-polymerization in presence of ZnBr as a reagent and cross linker is bromomethyl methyl ether. The absorbent black materials with a 3D network were prepared by direct carbonization and activation of the as-prepared PA. The hydrothermal method was adapted for the preparation of carbon hybrid material C@NiMn2O4 powder's catalytic activity is effective in reducing p-nitrophenol to p-aminophenol and decolorizing carbon-based dyes like methyl orange (MO), methyl yellow (MY), and Congo red (CR) in aqueous media at 25 °C when NaBH4 is added. UV–visible spectroscopy was used to analyze the dyes' breakdown at regular interval.

Herein, the present work focuses on the effective counter electrode for dye-sensitized solar cells. The bottom–up approach was adapted to synthesize Mn2O3 nanorods via the hydrothermal method and the reduced graphene oxide was merged with Mn2O3 to prepare a nanocomposite. The prepared nanocomposites were subjected to physio-chemical and morphological characterizations which revealed the crystalline nature of Mn2O3 nanorods. The purity level rGO was characterized using the Raman spectrum and the Fourier transform infrared spectroscopy employed to find the functional groups. The morphological micrographs were visualized using SEM and TEM and the high aspect ratio Mn2O3 nanorods were observed with 5–7 nm and supported by rGO sheets. The electrocatalytic nature and corrosion properties of the counter electrode towards the iodide electrolyte were studied using a symmetrical cell. The as-synthesized nanocomposites were introduced as counter electrodes for DSSC and produced 4.11% of photoconversion efficiency with lower charge transfer resistance. The fabricated DSSC devices were undergone for stability tests for indoor and outdoor atmospheres, the DSSC stability showed 93% and 80% respectively for 150 days.

The untreated effluent dropping into the environment from various textile industries is a major issue. To solve this problem, development of an efficient catalyst for the degradation of macro dye molecules has attracted extensive attention. This work is mainly focused on the synthesis of nickel–manganese sulfide decorated with rGO nanocomposite (Ni–Mn-S/rGO) as an effective visible photocatalyst for degradation of textile toxic macro molecule dye. A simple hydrothermal method was used to synthesize Ni–Mn-S wrapped with rGO. The prepared composites were characterized using various techniques such as X-ray diffraction (XRD), high-resolution scanning electron microscopy (HR-SEM), high-resolution transmission electron microscopy (HR-TEM), Fourier transform infra-red spectrometer (FTIR), and ultra violet–visible (UV–Vis) spectroscopy. The photocatalytic performance of nickel sulfide (NiS), manganese sulfide (MnS), nickel–manganese sulfide (Ni–Mn-S), and Ni–Mn-S/rGO nanocomposite was assessed by analyzing the removal of acid yellow (AY) and rose bengal (RB) dyes under natural sun light. Among these, the Ni–Mn-S/rGO nanocomposite showed the high photocatalytic degradation efficiency of AY and RB dyes (20 ppm concentration) with efficiency at 96.1 and 93.2%, respectively, within 150-min natural sunlight irradiation. The stability of photocatalyst was confirmed by cycle test; it showed stable degradation efficiency even after five cycles. This work confirms that it is an efficient approach for the dye degradation of textile dyes using sulfide-based Ni–Mn-S/rGO nanocomposite.

Photoanode optimization is a fascinating technique for enlightening the power conversion efficiency (PCE) of dye-sensitized solar cells (DSSCs). In this present study, V2O5/ ZnO and reduced graphene oxide (rGO)-V2O5/ZnO nanocomposites (NCs) were prepared by the solid-state technique and used as photoanodes for DSSCs. A wet chemical technique was implemented to generate individual V2O5 and ZnO nanoparticles (NPs). The structural characteristics of the as-synthesized NCs were investigated and confirmed using powder X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), and Scanning electron microscope (SEM) with energy dispersive X-ray (EDX) analysis. The average crystallite size (D) of the as-synthesized V2O5/ ZnO and rGO-V2O5/ZnO NCs was determined by Debye-Scherer’s formula. The bandgap (eV) energy was calculated from Tauc’s plots, and the bonding nature and detection of the excitation of electrons were investigated using the Ultra violet (UV) visible spectra, Fourier Transform infrared (FTIR) and photoluminescence (PL) spectral analysis. Electrical studies like Hall effect analysis and the Nyquist plots are also described. The V2O5/ ZnO and rGO-V2O5/ZnO NCs based DSSCs exhibited 0.64% and 1.27% of PCE and the short circuit current densities and open circuit voltages improved from 7.10 to 11.28 mA/cm2 and from 0.57 to 0.68 V, respectively.

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.

본 연구에서는 자기공명영상 검사 시 와인색 반영구 문신용 염료가 신호 강도에 미치는 영향을 분석하고, 전자파흡수 에 의한 발열 감소 방안을 연구하고자 하였다. 한천과 와인색 반영구 문신용 염료를 이용하여 염료가 퍼진 형태의 팬텀(패드형 팬텀)과 한곳에 뭉친 형태의 팬텀(주사형 팬텀)을 제작하였다. 두 팬텀은 전신용 자기공명영상장치에서 고속스핀에코(turbo spin echo, TSE)와 경사에코(gradient echo, GRE) 계열의 펄스열을 이용하여 2D와 3D로 검사하였다. 검사 후 영상 분석은 팬텀의 몸체, 염료, 공기 방울, 배경을 대상으로 총 720회의 신호강도를 측정하였 다. 전자파흡수에 의한 발열 감소 방안을 확인하기 위해 삽입형 온도계를 팬텀에 삽입 후 검사 전후 팬텀의 온도 변화를 확인하였다. 이때, 대기 온도의 상승 변화를 고려하기 위해 검사 전 대기 온도를 측정하였고, 발열 감소를 위한 방법으로 장치에 내장된 팬, 젖은 거즈, 얼음을 이용하였다. 신호 강도는 2D 영상보다 3D 영상이 좋았고, TSE 계열이 GRE 계열보다 좋았다. 특히 와인색 반영구 문신용 염료가 있는 부위의 신호강도는 공기 때문에 발생한 자화 율 인공물보다 신호강도가 낮게 측정되었다. 온도 측정 검사는 패드형 팬텀과 주사형 팬텀 모두 검사에 의한 온도상 승 효과가 있었으며 온도의 저감을 위한 방법으로 얼음 패드, 팬, 젖은 거즈 순서였다. 본 연구를 통해 와인색 반영구 문신용 염료는 자기공명영상 검사에서 영상과 환자의 안전에 문제를 일으킬 수 있음을 확인하였고, 발열 감소 방안으 로 얼음 패드가 효과적이었다는 것을 확인할 수 있었다.

효소 고정화 막 생물반응기(EMBRs)는 폐수 내의 염료를 처리하는 새로운 방법입니다. 이 분야는 효소의 효능과 환경에 대한 높은 저항성 때문에 많은 양의 연구가 진행되었습니다. 효소 자체와 해당 효소의 구조를 모두 포함하는 다양한 방법이 EMBR에 접근할 수 있습니다. 생물반응기 자체는 염료 제거의 필요에 맞게 변형될 수 있습니다. 효소적 생물반응기 부터 산화 그래핀 또는 탄소 나노튜브와 같은 나노구조를 사용하는 것까지 다양합니다. 또한 TiO2와 같은 나노입자는 EMBR 을 더욱 향상시키기 위해 사용될 수 있습니다. 폴리머 기반의 막 지지 구조는 또한 효능 증가의 문제에 접근하는 다양한 방 법을 포함합니다. 본 바와 같이, 지난 수십 년 동안 EMBR을 사용하는 이 문제에 대한 다양한 접근법이 수행되었습니다. 이 검토는 방법론을 요약하고 EMBR에 대한 다양한 개선 사항을 설명하는 것을 목표로 합니다.

An eco-friendly material was synthesized through interfacial polymerization of aniline on particles of g-C3N4 with arginine, resulting in Arg-PANI@g-C3N4 composite. The as-synthesized composite was characterized by the Brunauer, Emmett, and Teller (BET) surface area, X-ray energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The adsorption capability of as-synthesized composite towards Orange G (OG) dye has been evaluated under several experimental conditions, such as the adsorbent dosage, initial dye concentration, contact time under agitation, pH of dye solution and temperature. Thermodynamics parameters such as free energy (ΔG°), entropy (ΔS°), and enthalpy (ΔH°) were also calculated and suggested that the adsorption process is spontaneous and endothermic in nature. The kinetics data revealed that the adsorption of OG dye onto Arg-PANI@g-C3N4 follows the pseudo-second order kinetics model. The maximum adsorption capacity was found to be 80.54 mg·g−1. Furthermore, the Arg-PANI@g-C3N4 surface exhibited a Langmuir-like adsorption isotherm in contrast to a Freundlich isotherm due to homogeneous active site distribution. Regeneration investigation showed the excellent reusability of Arg-PANI@g-C3N4 composite during the cleaning up of solution containing OG dye molecules.

이번에 제시할 화상 사례 보고는 환자와 검사를 시행하는 방사선사의 부주의로 인한 화상 안전사고가 아니라 환자 가운 의 치수 구별을 하기 위하여 사용한 녹색 염료가 착색된 파이핑 라인에서 발생한 복부 부위 화상 안전사고에 대한 MRI 인공물 영상과 사례를 보고하고자 함이다. 화학 착색염료는 다양한 금속을 사용하여 만들어지고 주로 금속 염화물로 이루 어져 있으며 이번에 화상 사례로 발생한 녹색 염료는 열 전도성이 높은 구리와 크롬, 철 성분이 많이 함유된 염화물이 주로 사용되고 있다. 이러한 화상 안전사고를 막기 위해서는 염료의 성분에 대해서 알아보고 열 전도성이 없는 스펀지나 면으로 된 포 등을 피부와 환자 가운 사이에 끼워 간격을 두어야 할 것이다. 이번 화상 사례는 철저한 검사 전 선별 절차에도 불구 하고 화상 안전사고가 발생할 수 있음을 보여 주고 있으며 MRI 인공물 영상을 확인하여 조치하면 화상 안전사고를 미리 예방할 수 있는 정보로 가치가 있을 것으로 생각된다.

How to effectively deal with the polluted water by the pollutant of organic dyes is the world problem. It is of great significance if the organic dyes in the polluted water can be directly turned into the useful materials through a facile approach. Herein, the water which contains the common organic dye, Reactive red 2 (RR2), has been chosen to be the model to synthesize graphene quantum dots (GQDs) by a facile route. The comprehensive characterizations, including TEM (HRTEM), XPS, Raman, PL and UV–Vis. spectra, have been performed to confirm the structures and explore the properties of the synthesized GQDs. Meanwhile, the excellent PL properties and low biotoxicity of the GQDs confer them with the potential applications in the biological fields. When the GQDs are excited by the wavelength of 360 nm, the maximum emission is achieved at 428 nm. It is well demonstrated that the synthesized GQDs are able to detect the Al3+ which causes multiple diseases, such as Parkinson, Alzheimer, kidney disease, and even cancer. The detection range is from 90 to 800 μM, which is different from the reported kinds of the literature. Therefore, this work not only provides an economical and environmental route on solving the universal problem from organic dyes, but also facilitates to advancing the synthesis and application of GQDs.

목적 : 반응성 청색광차단 염료를 하이드로겔 콘택트렌즈에 화학적으로 고정시켰고, 제조된 콘택트렌즈의 청색 광차단 기능의 분석 및 첨가된 염료를 정량하고자 한다. 방법 : Vinyl sulfone-기반의 반응성 염료인 Reactive Orange 16 Dye를 다량의 알콜 작용기를 함유하는 하 이드로겔 콘택트렌즈에 화학적으로 결합시켰다. 콘택트렌즈의 청색광차단 특성 및 염료의 정량은 UV-vis spectrophotometer를 이용하여 확인하였다. 결과 : 청색광차단기능의 Reactive Orange 16 Dye가 성공적으로 하이드로겔 콘택트렌즈에 결합되었다. UV-vis spectra 분석을 통해 염료를 함유한 콘택트렌즈들이 우수한 청색광차단 기능을 보임을 확인하였다. Beer-Lambert의 법칙을 이용하여, 콘택트렌즈에 첨가된 Reactive Orange 16 Dye를 정량하였으며, 반응 염료 의 농도 조절을 통해, 콘택트렌즈의 청색광차단율을 조절할 수 있었다. 결론 : 본 연구에서는 청색광차단 기능의 반응성 염료를 하이드로겔 콘택트렌즈에 화학적 결합을 통해 고정시 키고, 청색광차단 기능을 분석하였다. 화학적 반응에서 청색광차단 염료의 농도가 증가할수록, 380~500 nm 사 이의 청색광 파장 영역에서의 차단 세기와 첨가된 염료의 양이 같이 증가함을 확인하였다. 대량생산이 가능한 청 색광차단 콘택트렌즈의 개발은 기능성 안광학의료기기 개발에 큰 역할을 할 것으로 기대된다.