본 논문은 인도 영어극에서 가장 중요한 목소리 중 하나인 아시프 쿠림 보이의 선택된 희곡들에 나타난 식민주의의 주제와 재현 방식을 고찰한다. 쿠림보이의 희곡들은 식민주의의 개념과 그 다양한 양상을 드러내며, 자본주의가 독립 이후 인도 사회 전반에 미친 영향을 바탕으로 식민주의의 비인간화 행위를 지적한다. 그의 희곡들은 학문적 연구의 대상으로 다루어졌으며, 일부는 지역어로 번역되기도 하였다. 쿠 림보이의 작품은 역사와 정치 등 폭넓은 주제를 포괄하고 있으며, 인종, 계급, 젠더와 같은 문제들이 많은 작품에서 부각되지만 이에 대한 심층적인 논의는 아직 부족하다. 그는 시대의 중대한 문제들에 대한 지속적인 관심을 통해 삶에 대한 독자적인 시각을 형성하며, 동시대적 주제에 대한 뚜렷한 입장을 가진 독특한 극작가로 평가된다. 또한 그는 현대 사회의 비참한 현실을 가감 없이 드러내는 데 주력한다.

인도 연극의 선구자인 비제이 텐둘카르는 인도 연극을 전통적 뿌리에서 현대적이고 혼종적인 형태로 탈바꿈시키는 데 중추적인 역할을 하였다. 본 논문은 텐 둘카르의 작품이 어떻게 토착 문화 요소와 서구 모더니즘의 영향을 결합하며 인도 연 극의 진화를 반영하는지를 탐구한다. 산스크리트 희곡과 마하바라타, 라마야나와 같은 서사에 뿌리를 둔 전통 인도 연극은 도덕적 이분법과 사회 규범에 중점을 두었다. 그 러나 탈식민 시대의 인도 영어 연극, 특히 텐둘카르의 작품은 도시 중산층이 직면한 현대 사회 정치적 문제들을 다루는 방향으로 전환되었다. 텐둘카르의 􋺷정숙! 재판이 진행 중이다􋺸는 가부장제, 성 역할, 사회적 위선과 같은 주제를 조명하며 그 전환을 대표하는 사례 연구로 제시된다. 이 희곡은 모의 재판이라는 개념을 통해 사회적 불의 와 여성 억압을 비판하며, 현대 인도 사회의 보다 넓은 투쟁을 상징한다. 텐둘카르의 인도주의적 접근은 기존의 규범에 도전하며 진정성, 성실성, 새로운 도덕 질서를 옹호 한다. 그의 심리적, 실존적, 여성주의적 문제에 대한 집중은 현대 삶의 분열성을 부각 시킨다. 본 논문은 텐둘카르만의 독특한 시각을 분석함으로써, 인도 연극이 사회 비판 과 문화적 혼종성의 장으로 진화한 과정을 보여준다.

Galaxy evolution studies require the measurement of the physical properties of galaxies at different redshifts. In this work, we build supervised machine learning models to predict the redshift and physical properties (gas-phase metallicity, stellar mass, and star formation rate) of star-forming galaxies from the broad-band and medium-band photometry covering optical to near-infrared wavelengths, and present an evaluation of the model performance. Using 55 magnitudes and colors as input features, the optimized model can predict the galaxy redshift with an accuracy of σ(Δz/1+z) = 0.008 for a redshift range of z < 0.4. The gas-phase metallicity [12 + log(O/H)], stellar mass [log(Mstar)], and star formation rate [log(SFR)] can be predicted with the accuracies of σNMAD = 0.081, 0.068, and 0.19 dex, respectively. When magnitude errors are included, the scatter in the predicted values increases, and the range of predicted values decreases, leading to biased predictions. Near-infrared magnitudes and colors (H, K, and H −K), along with optical colors in the blue wavelengths (m425–m450), are found to play important roles in the parameter prediction. Additionally, the number of input features is critical for ensuring good performance of the machine learning model. These results align with the underlying scaling relations between physical parameters for star-forming galaxies, demonstrating the potential of using medium-band surveys to study galaxy scaling relations with large sample of galaxies.

Complex structure constituting of several layers of heteroatom-doped N-CDs are used as a main sensing film along with aluminum electrodes in conductometric gas sensing system for sensitive and selective monitoring of CO2 and CO gases diluted with normal air, which are extensively prevalent in the atmosphere primarily due to the industrial revolution, locomotives, and numerous natural phenomena’s and the limit of detection (LOD) turned out to be 400 ppm and 30 ppm, respectively, with 20% relative humidity at 30 °C and pressure 1 (atm) which are good for healthy air quality checks. The sensor performance was satisfactory and bidirectional at ambient room temperature (30 °C) and pressure (1 atm) conditions but the relative humidity (50%) at 30 °C had a detrimental impact on the sensing responses, therefore intermittent heating at 80 °C for several minutes between the sensing responses was provided to the sensing chip or one should use gas filter membranes to block humidity, thereby maintaining its constant performance with great ease and accuracy. The cyclic voltammetry revealed well-defined oxidation and reduction peaks, with excellent stability and reversibility. In a nutshell, heteroatom-doped N-CDs’ nanocomposite material can revolutionize in a better environmental pollution monitoring by sensing gases in an extensively lesser response and recovery times.

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.

Structural inversion refers to the reverse reactivation of extensional faults that influence basin shortening accommodated by contractional faults or folds. On the Korean peninsula, Miocene inversion structures have been found, but the Cretaceous rocks on Geoje Island may have undergone inversion as early as the Upper Cretaceous. To evaluate the structural inversion on Geoje Island, located on the eastern side of South Korea, and to determine the effects of preexisting weakness zones, field-based geometric and kinematic analyses of faults were performed. The lithology of Geoje Island is dominated by hornfelsified shale, siltstone, and sandstone in the Upper-Cretaceous Seongpori formation. NE and NW-oblique normal faults, conjugate strike-slip (NW-sinistral transpressional and E-W-dextral transtensional) faults, and NE-dextral transpressional faults are the most prominent structural features in Geoje Island. Structural inversion on Geoje Island was evidenced by the sinistral and dextral transpressional reactivation of the NW and NE-trending oblique normal faults respectively, under WNW-ESE/NW-SE compression, which was the orientation of the compressive stress during the Late Cretaceous to Early Cenozoic.

Biomass-derived porous carbon is an excellent scientific and technologically interesting material for supercapacitor applications. In this study, we developed biomass-derived nitrogen-doped porous carbon nanosheets (BDPCNS) from cedar cone biomass using a simple KOH activation and pyrolysis method. The BDPCNS was effectively modified at different temperatures of 600 °C, 700 °C, and 800 ℃ under similar conditions. The as-prepared BDPCNS-700 electrode exhibited a high BET surface area of 2883 m2 g− 1 and a total pore volume of 1.26 cm3 g− 1. Additionally, BDPCNS-700 had the highest electrical conductivity (11.03 cm− 1) and highest N-doped content among the different electrode materials. The BDPCNS-700 electrode attained a specific capacitance of 290 F g− 1 at a current density of 1 A g− 1 in a 3 M KOH electrolyte and an excellent longterm electrochemical cycling stability of 93.4% over 1000 cycles. Moreover, the BDPCNS-700 electrode had an excellent energy density (40.27 Wh kg− 1) vs power density (208.19 W kg− 1). These findings indicate that BDPCNS with large surface areas are promising electrode materials for supercapacitors and energy storage systems.

In this study, UiO-66-NH2 was synthesized and incorporated with graphene aerosol (UiO-66-NH2/GA) and ethylenediamine functionalized graphene oxide (UiO-66-NH2/GO-NH2). These composites were characterized using infrared spectroscopy, powder X-ray diffraction, ultraviolet–visible light spectroscopy, scanning electron microscope, and energy-dispersive X-ray spectroscopy. UiO-66-NH2/GO-NH2 exhibited 93% adsorption of quinoline in 5 h, UiO-66-NH2 and UiO-66-NH2/GA presented 80.4% and 86.5%, respectively. The high adsorption observed on UiO-66-NH2/GO-NH2 was attributed to the unique electronic properties, and hydrogen bonding between the nitrogen atom of quinoline and NH2- phenyl fragment of UiO-66-NH2, and N–H of ethylenediamine. GO also offered combined strong π–π interactions on its surface, and the oxygen coverage (~ 50%) on GO within the structure is responsible for the formation of strong hydrogen bonds with quinoline. Theoretical calculation suggested that UiO-66-NH2/GO-NH2 presented a more favourable adsorption energy (− 18.584 kcal/ mol) compared to UiO-66-NH2 (− 16.549 kcal/mol) and UiO-66-NH2/GA (− 13.991 kcal/mol). These results indicate that nanocomposites have a potential application in quinoline capture technologies in the process of adsorptive denitrogenation.

By polymerizing acrylonitrile in the presence of ammonium persulfate as an initiator and Pterocladia capillacea-activated carbon (P-AC) as a filler, a composite material polyacrylonitrile/Pterocladia capillacea-activated carbon (PAN/P- AC) was developed. By reacting hydroxylamine with the composite's nitrile groups, the prepared composite was functionalized by amidoximation. FTIR spectrometry, thermogravimetric analysis (TGA), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Brunauer–Emmett–Teller (BET) analysis were all applied to thoroughly characterize the fabricated adsorbent. For the treatment of Cr(VI) ions from synthetic solutions, the adsorption properties of amidoximated polyacrylonitrile/Pterocladia capillacea-activated carbon (PAO/P-AC) were investigated. The pH effect, uptake kinetics, adsorption isotherms, and thermodynamics studies were used to characterize adsorption properties. As a kinetic model analysis, the data confirmed that the pseudo-second-order rate equation matched well the adsorption process. With coefficients of determination (R2) of 0.9998, the Tempkin isotherm model had the lowest error, suggesting that it is the best fitted model to describe this adsorption mechanism. Thermodynamic parameters demonstrated that Cr(VI) adsorption was endothermic.

Sugarcane bagasse has been used as a substrate for the development of microporous nano-activated carbons for the treatment and elimination of dissolved materials from aquatic environment. The activated carbon was produced using chemical activation in one-step method with zinc chloride ( ZnCl2) as the activating agent at a carbonization temperatures range from 500 to 900 °C. The effects of temperature and time of carbonization on the activated carbon product properties were thoroughly studied. The activated carbons that resulted were characterized using the N2 adsorption/desorption isotherms, Brunauer–Emmett–Teller method (BET), pore property analysis, micropore (MP) surface area, t-plot surface area, TGA, FTIR, SEM, TEM, and EDX analyses. The prepared activated carbon’s point of zero charge, Boehm titration process, iodine removal percentage, and methylene blue number were also investigated. The prepared activated carbon’s maximum surface area was achieved using a 2/1 impregnation ratio (dried sugarcane bagasse/ZnCl2) at 600 °C temperature of carbonization and 60 min residence time. 1402.2 m2/ g, 0.6214 and 1.41 cm3/ g, respectively, were the largest surface area, total pore volume, and micropore volume. As the activation temperature increased, the total pore volume increased and the BET study measured a pore diameter of 0.7 nm and a mean pore diameter of 1.77 nm.

This work reports utilization of apple leaves as a source of activated carbon. Activated carbon from apple leaves is prepared by two different methods, thermal activation where AC1 is obtained and chemical activation using H3PO4 and ZnCl2 where AC2 and AC3 are obtained, respectively. XRD analysis revealed that all types of prepared ACs have a semi-crystalline nature with a mean crystallite size of 13, 21.02, and 39.47 nm for AC1, AC2, and AC3, respectively. To identify the most suitable desorption temperature, the exothermic behavior was discovered for the three types of ACs by DSC. The exothermic onset temperatures are 340 °C, 200 °C, 400 °C, or AC1, AC2, and AC3, respectively. The point of zero charge for the three types of ACs is 8.6, 7.3, and 2.5 for AC1, AC2, and AC3, respectively. The BET surface area analysis data demonstrated that mesoporous structure was developed in AC1 and AC2, while a microporous structure was developed in AC3. Quantum chemical calculations for ACs is carried out using Density Functional Theory (DFT). Application of the prepared ACs in adsorption of basic dye C.I. base blue 47 is studied. The maximum removal efficiency was 65.1%, 96% and 99% for AC1, AC2, and AC3, respectively under the influence of different operating aspects. Adsorption data are modeled by Langmuir, Freundlich, and Temkin isotherms. The data revealed that adsorption of basic dye C.I. base blue 47 on AC1 follows Langmuir isotherm and adsorption on AC2 and AC3 follows Freundlich isotherm.