Photochemical behaviour and toxicity evolution of phenylbenzoate liquid crystal monomers in water.

Liquid crystal monomers (LCMs) are a group of emerging pollutants that pose potential environmental risks because of their ubiquitous occurrence and toxicity. Understanding their environmental transformation is essential for assessing the ecological risk. In this study, we investigated the photochemical transformation kinetics, mechanism, and photo-induced toxicity of three phenylbenzoate LCMs in water. Their apparent photolytic rate constants were within (0.023 - 0.058) min-1, and the half-lives were < 30.0 min, showing lower persistence in water. Dissolved organic matter significantly inhibited their photolysis because of light-shielding effect and quenching of excited triplet states of LCMs. Their photolysis mainly occurred through excited triplet states, and the reactive oxygen species (i.e., ⋅OH, 1O2 and ⋅O2-) contributed to their degradation. The main photolysis pathways were ester bond cleavage, ⋅OH substitution/addition, and defluorination. Experiments and computational simulation revealed that some ·OH addition/substitution products have similar toxicity with LCMs. Additionally, the ∙OH reaction rate constants (kOH) of LCMs were determined to be > 1 × 109 M-1 s-1, evidence for their high reactivity toward ⋅OH. We have further developed reliable methods to estimate kOH of other phenylbenzoate-like LCMs with quantum chemical calculations. These results are useful for understanding the transformation and fate of LCMs in aquatic environments.

Chitin nanofibrils assisted 3D printing all-chitin hydrogels for wound dressing.

The direct ink writing technique used in 3D printing technology is generally applied to designing biomedical hydrogels. Herein, we proposed a strategy for preparing all-chitin-based inks for wound dressing via direct ink writing technique. The ß-chitin nanofibers (MACNF) with a high aspect ratio were applied as a nanofiller to modulate the rheological properties of the alkaline dissolved chitin solution. The printing fidelity significantly depends on the MACNF introduction amount to the composite ink. 5-10 wt% MACNF ratio showed superior printing performance. The printed scaffold showed a uniform micron-sized pore structure and a woven network of nanofibers. Due to the good biocompatibility of chitin and the stereoscopic spatial skeleton, this scaffold showed excellent performance as a wound dressing, which can promote cell proliferation, collagen deposition and the angiogenesis of wounds, demonstrating its potential in biomedical applications. This approach successfully balanced the chitinous printability and biofunctions.

Preparation of Oily Sludge-Derived Activated Carbon and Its Adsorption Performance for Tetracycline Hydrochloride.

Oily sludge-derived activated carbon was prepared using the potassium hydroxide (KOH) activation method using oily sludge as a raw material, and one-factor experiments determined the best conditions for preparing activated carbon. The activated carbon's morphological structure and surface chemical properties were analyzed by scanning different characterization tools, and the adsorption behavior of tetracycline hydrochloride was investigated. The results showed that the optimum conditions for preparing oily sludge-derived activated carbon were an activation temperature of 400 °C, activation time of 30 min, activator concentration of 1 mol/L, and impregnation ratio of 2 mL/g. After activation, the activated carbon had more pores and a more orderly crystal structure arrangement, the specific surface area was 2.07 times higher than that before activation, and the surface was rich in functional groups such as -HO, -C-O, -C=C, and -C-H, which increased the active sites of activated carbon. Physicochemical effects dominated the adsorption process. It belonged to the spontaneous heat absorption process under the quasi-secondary kinetic and Langmuir isothermal models. The maximum monolayer adsorption capacity of KOH-activated carbon was 205.1 mg·g-1.

Enhancing CO2 capture through innovating monolithic graphene oxide frameworks.

The advancement and engineering of novel crystalline materials is facilitated through the utilization of innovative porous crystalline structures, established via KOH-treated monolithic graphene oxide frameworks. These materials exhibit remarkable and versatile characteristics for both functional exploration and applications within the realm of CO2 capture. In this comprehensive study, we have synthesized monolithic reduced graphene oxide-based adsorbents through a meticulous self-assembly process involving different mass ratios of GO/malic acid (MaA) (1:0.250, 1:0.500, and 1:1 by weight). Building upon this foundation, we further modified MGO 0.250 through KOH-treatment by chloroacetic acid method, leading to the creation of MGO 0.250_KOH, which was subjected to CO2 capture assessments. The comprehensive investigation encompassed an array of parameters including morphology, specific surface area, crystal defects, functional group identification, and CO2 capture efficiency. Employing a combination of FT-IR, XRD, Raman, BET, SEM, HR-TEM, and XPS techniques, the study revealed profound insights. Particularly notable was the observation that the MGO 0.250_KOH adsorbent exhibited an exceptional CO2 capture performance, leading to a significant enhancement of the CO2 capture capacity from 1.69 mmol g-1 to 2.35 mmol g-1 at standard conditions of 25 °C and 1 bar pressure. This performance enhancement was concomitant with an augmentation in surface area, elevating from 287.93 to 419.75 m2 g-1 (a nearly 1.5-fold increase compared to MGO 1.000 with a surface area of 287.93 m2 g-1). The monolithic adsorbent demonstrated a commendable production yield of 82.92%, along with an impressive regenerability of 98.80% at 100 °C. Additionally, adsorbent's proficiency in CO2 adsorption, rendering it a promising candidate for post-combustion CO2 capture applications. These findings collectively underscore the capacity adsorbents to significantly amplify CO2 capture capabilities. The viability of employing this strategy as an uncomplicated pre-treatment technique in various industrial sectors is a plausible prospect, given the study's outcomes.

Soluble starch-derived porous carbon microspheres with interconnected and hierarchical structure by a low dosage KOH activation for ultrahigh rate supercapacitors.

The developed porous structure and high density are essential to enhance the bulk performance of carbon-based supercapacitors. Nevertheless, it remains a significant challenge to optimize the balance between the porous structure and the density of carbon materials to realize superior gravimetric and areal electrochemical performance. The soluble starch-derived interconnected hierarchical porous carbon microspheres were prepared through a simple hydrothermal treatment succeeded by chemical activation with a low dosage of KOH. Due to the formation of interconnected spherical morphology, hierarchical porous structure, reasonable mesopore volume (0.33 cm3 g-1) and specific surface area (1162 m2 g-1), the prepared carbon microsphere has an ultrahigh capacitance of 394 F g-1 @ 1 A g-1 and a high capacitance retention of 62.7 % @ 80 A g-1. The assembled two-electrode device displays good cycle stability after 20,000 cycles and an ultra-high energy density of 11.6 Wh kg-1 @ 250 W kg-1. Moreover, the sample still exhibits a specific capacitance of 165 F g-1 @ 1 A g-1 at a high mass loading of 10 mg cm-2, resulting in a high areal capacitance of 1.65 F cm-2. The strategy proposed in this study, via a low-dose KOH activation process, provides the way for the synthesis of high-performance porous carbon materials.

Effects of water washing and KOH activation for upgrading microalgal torrefied biochar.

Torrefaction is an effective pathway for microalgal solid biofuel upgrading, and alkali metal activation is also an efficient method to enhance fuel properties. This study explores the comparison of torrefaction alone and KOH activation combined with torrefaction to determine a better operation for biochar production from the microalga Nannochloropsis Oceanica. The results indicate that the HHV ranges of KOH-activated biochar and unactivated biochar are 25.611-32.792 MJ·kg-1 and 25.024-26.389 MJ·kg-1, respectively. Furthermore, KOH-activated biochar is better than unactivated biochar, with less residue, broader pyrolysis and combustion temperature ranges, higher elemental carbon, and less combined carbon. Moreover, KOH-activated biochar is close to the unactivated one from the viewpoint of expense calculation and life cycle assessment and thus possesses a better comprehensive performance. Overall, KOH activation is an efficient method for upgrading microalgal solid biofuel. The results are conducive to exploring further modification of microalgal solid biofuel production with better properties, thus leading to a greener and more efficient approach for upgrading fuel performance.

Synthesis and characterizations of conocarpus- and azadirachta-derived activated carbons as wastewater recycling material.

Water being the most important fluid supporting the life as well as industry is getting sparse and polluted day by day. Activated carbon (AC) can be utilized in various applications of significant environmental impact and sustainable living such as carbon dioxide sensing and capturing, air purification, and water recycling. However, in the wake of the recent corona pandemic which resulted in global lockdown and took the entire world by shock, a cost-effective and simple synthesis of such a useful material remains dire need of time. Therefore, this paper describes a simple and cost-effective synthesis of activated carbon (AC) of high porosity and surface area derived from the pruning of conocarpus and azadirachta trees. In reference to the study under consideration, alongside numerous others, a furnace was employed to synthesize activated carbon. However, our approach utilized a more conventional methodology wherein the environmental parameters were not optimized. In furnace-based procedures, factors such as temperature, pressure, and humidity are meticulously regulated, contrasting with the conventional methodologies where such parameters lack optimal control. Consequently, employing a furnace does not constitute a cost-effective approach for the physical activation of organic samples thus proving a furnace is not imperative for physical activation. The synthesis was carried out by physical activation in the form of carbonization followed by chemical activation with potassium hydroxide (KOH). The influence of activated carbon from each pruning over filtration of water containing industrial dye was investigated. Activation temperature and impregnation ratio of 600-800 °C and 1:5 were selected respectively. X-ray diffraction patterns (XRD) for all AC samples indicted the appearance of broad peaks at 2θ value of 20-30° which confirms the presence of carbon in the sample. The physical morphology arrangement by SEM analysis showed uneven arrangement of pores of conocarpus which indicated higher iodine number and hence higher adsorption capacity of 442.13 mg/g.

Comparative analysis for the impacts of VOC subgroups and atmospheric oxidation capacity on O3 based on different observation-based methods at a suburban site in the North China Plain.

The persistent O3 pollution in the Beijing-Tianjin-Hebei (BTH) region remains unresolved, largely due to limited comprehension of O3-precursor relationship and photochemistry drivers. In this work, intraday O3 sensitivity evolution from VOC-limited (volatile organic compound) regime in the forenoon to transition regime in the late afternoon was inferred by relative incremental reactivity (RIR) in summer 2019 at Xianghe, a suburban site in BTH region, suggesting that VOC-focused control policy could combine with stringent afternoon NOx control. Then detailed impacts of VOC subgroups on O3 formation were further comprehensively quantified by parametric OH reactivity (KOH), O3 formation potential (OFP), as well as RIR weighted value and O3 formation path tracing (OFPT) approach based on photochemical box model. O3 episode days corresponded to stronger O3 formation, depicted by higher KOH (10.4 s-1), OFP (331.7 µg m-3), RIR weighted value (1.2), and F(O3)-OFPT (15.5 ppbv h-1). High proportions of isoprene and OVOCs (oxygenated VOCs) to the total KOH and the OFPT method were demonstrated whereas results of OFP and RIR-weighted presented extra great impacts of aromatics on O3 formation. The OFPT approach captured the process that has already happened and included final O3 response to the original VOC, thus reliable for replicating VOC impacts. The comparison results of the four methods showed similarities when utilizing KOH and OFPT methods, which reveals that the potential applicability of simple KOH for contingency VOC control and more complex OFPT method for detailed VOC- and source-oriented control during policy-making. To investigate propulsion of VOC-involved O3 photochemistry, atmospheric oxidation capacity (AOC) was quantified by two atmospheric oxidation indexes (AOI). Both AOIp_G (7.0 × 107 molec cm-3 s-1, potential AOC calculated by oxidation reaction rates) and AOIe_G (8.5 µmol m-3, estimated AOC given redox electron transfer for oxidation products) were stronger on O3 episode days, indicating that AOC promoted the radical cycling initiated from VOC oxidation and subsequent O3 production. Result-oriented AOIe_G reasonably characterized actual AOC inferred by good linear correlation between AOIe_G and O3 concentrations compared to process-oriented AOIp_G. Therefore, with continuous NOx abatement, AOIe_G should be considered to represent actual AOC, also O3-inducing ability.

Time-efficient etching of LR-115 SSNTD film for indoor radon, thoron quantification.

LR-115 Solid State Nuclear Track Detector (SSNTD) is commonly utilized for quantifying indoor radon-thoron levels, by tallying the tracks formed in the films by exposure to these gases. Conventionally, sodium hydroxide (NaOH) is used to etch LR-115 films for 90 min at 60°C. However, this study suggests a time-efficient alternative approach utilizing potassium hydroxide (KOH) as the etchant. In an initial investigation, the bulk etch rates of KOH were examined at different normalities and temperatures, revealing that KOH exhibited nearly double the bulk etch rates compared to NaOH. Subsequently, a specially designed controlled experiment was conducted to assess the efficacy of the technique by enumerating the tracks generated in the films. Both etchants demonstrated very similar track counts for identical controlled exposures, indicating the reliability of the method. A consistent behavior was observed in the real-case scenario of LR-115 films exposed indoors to alpha particles from radon and its decay products. In both experiments, the etching with KOH for 45 min gave track densities comparable to standard NaOH etching for 90 min, highlighting the time efficiency of this method. Investigations were carried out into track shape and size features, aspects crucial to the measurement technique, using microscopic imaging of samples treated with both etchants. Strikingly similar track shapes and sizes were observed, affirming the consistency in the track measurement technique. Collectively, these findings suggest that KOH etchant reduces the etching time, presenting itself as a time-efficient method for quantifying radon and thoron track density.

Investigating the effectiveness of rice husk-derived low-cost activated carbon in removing environmental pollutants: a study of its characterization.

The chemically activated biochar was produced through the pyrolysis of rice husk. Thermal gravimetric and elemental analysis were conducted to characterize the raw rice husk. The activated biochar product underwent evaluation through SEM, BET and, FT-IR analysis. This cost-effective activated carbon was utilized as an adsorbent for the elimination of environmental pollutants. At a temperature of 25 °C, the activated biochar product exhibited an impressive maximum CO2 adsorption capacity of 152 mg/g. This exceptional performance can be attributed to its notable surface area and porosity, measuring at 2,298 m2/g and 0.812 cm3/g, respectively. This product was also utilized to remove methyl red (MR) dye from an aqueous solution. The optimal parameters for the removal of MR were determined as follows: a pH of 6.0, a temperature of 25 °C, an initial MR concentration of 50 mg/L, and an adsorbent dosage of 0.4 g/L. At a duration of 140 min, the system attained its maximum equilibrium adsorption capacity, reaching a value of 62.06 mg/g. Furthermore, the calculated maximum MR removal efficiency stood at an impressive 99.31%. The thermodynamic studies demonstrated that the MR removal process was spontaneous, exothermic, and increased randomness. Kinetic studies suggested that the pseudo-second-order model can fit well.

Rice is the staple food for a significant portion of the world's population. Rice husk, which is released during the production and processing of rice, is one of the most important agricultural wastes worldwide. In this study, low cost activated carbon was produced by converting renewable resource such as rice husk biomass into a product with high added value. The resulting product, with its high surface area, can offer a more sustainable, cost-effective, and versatile alternative for a range of industrial, environmental, and medical applications.

High efficiency removal of NO using waste calcium carbide slag by facile KOH modification.

Waste calcium carbide slags (CS), which are widely applied to desulfurisation, are not typically used in denitration. Herein, to well achieve waste control by waste, a facile and high-efficiency denitration strategy is developed using KOH to modify the calcium carbide slags (KCS). Various KCS samples were investigated using a series of physical and chemical characterisations. The performance test results showed that the KOH concentration and reaction temperature are the main factors affecting the denitration efficiency of KCS, and CS modified with 1.5 mol/L KOH (KCS-1.5) can achieve 100% denitration efficiency at 300°C. Such excellent removal efficiency is due to the catalytic oxidation of the oxygen-containing functional groups derived from the KCS. Further studies showed that KOH treatment significantly increased the concentration of oxygen vacancies, nitro compounds, and basic sites of CS. This study provides a novel strategy for the resource utilisation of waste CS in the future.

Investigations of NO reduction by coal-based activated carbon with KOH activation: Performance and mechanism.

Selective catalytic reduction of ammonia is the most widely used technology for NOx removal, but there have been serious ammonia leaks and a narrow reaction temperature window. To overcome these limitations, a coal-based activated carbon (CAC) approach using KOH activation for the ammonia-free reduction of NO was investigated in this work. A preparation process was investigated by evaluating the De-NOx performance at different mass ratios (KOH:coal = 0-3:1), and activation temperatures (700-900 °C). The optimum conditions were an activation temperature of 700 °C and a 1:1 ratio of KOH/coal, named CAC-1:1-700. Between 330 and 500 °C, the NO conversion efficiency is maintained at 100% within 90 min. The CAC-1:1-700 showed excellent denitrification performance and SO2 resistance. Based on BET, SEM, XRD, Raman, FT-IR, and XPS characterization analysis, it was found showed that KOH activation could increase the amorphous carbon, pore structure, and C(O) functional groups in CAC, which had positive effects on the denitrification performance. Furthermore, the evolution of char structures and surface species before and after the Char-NO-O2 reaction was evaluated by Raman and XPS, and the possible reaction mechanisms was proposed. Aliphatic structures and small aromatic rings can play the same role in De-NOx, O2 is adsorbed on the carbon to form an oxygen-containing functional group, generating more C-O groups and creating reactive sites C*. NO then interacts with these reactive sites and is reduced to N2. This research prepared CAC as a promising potential alternative to ammonia reductants due to its excellent denitration performance over a medium temperature range and complex flue gas environments, while providing the high-value utilization of coal resources.

Incidence of KOH Positive Elements in Chronic Discharging Ear -A Retrospective Study.

The term chronic suppurative otitis media (CSOM) refers to middle ear infections lasting more than three months that lead to perforated tympanic membrane. Low socioeconomic strata of the society are more likely to have the disease in developing countries. There have been many studies focusing on the bacterial flora of CSOM, but little is known about the mycological aspects, which have become increasingly important over the last few decades. The present study was aimed to speculate the presence of fungal flora responsible for the cases of CSOM among patients who attended the Ear, Nose, and Throat Department of our hospital a tertiary care center. This retrospective study was conducted in a tertiary care centre after taking the approval of the protocol review committee and institutional ethics committee. Total 100 Patients of chronic otitis media were included with no history using ear drops for last one week and using two sterile swab without touching the external auditory canal, discharge was taken from middle ear and placed in sterile container and sent for potassium hydroxide (KOH) mount and observed. The age ranged from 18 months to 87 years and the mean age was 37.27+/- 12.59 years. The study population of male is 42 (41.6%) and female is 59 (58.4%). Distribution of KOH positivity observed for 33 (32.7%) and KOH negative for the study population of 68 (67.3%). When antibacterial treatment does not seem to relieve persistent otorrhea, otologists should suspect mycotic otitis media probable cause.

An Effective Strategy to Synthesize Well-Designed Activated Carbon Derived from Coal-Based Carbon Dots via Oxidation before Activation with a Low KOH Content as Supercapacitor Electrodes.

The development of coal-based activated carbon for supercapacitors provides a robust and effective approach toward the clean and efficient use of coal, and it also offers high-quality and low-cost raw materials for energy storage devices. However, the one-step activation method for preparing coal-based activated carbon has problems, such as difficulty in introducing surface-functional groups and high KOH dosage. In our work, activated carbon was prepared through an effective strategy of oxidation and KOH activation with a low KOH content by employing coal-based carbon dots as raw material. The influence of temperature during the KOH activation of carbon dots on a specific surface area, pore structure, and various quantities and types of surface-functional groups, as well as on the electrochemical performance of supercapacitors, was systematically studied. The as-prepared sample, with the alkali-carbon ratio of 0.75, processes a large specific surface area (1207 m2 g-1) and abundant surface-functional groups, which may provide enormous active sites and high wettability, thus bringing in high specific capacitance and boosted electrochemical performances. The oxygen and nitrogen content of the activated carbon decreases while the carbon content increases, and the activation temperature also increases. The as-prepared activated carbon reaches the highest specific capacitance of 202.2 F g-1 in a 6 M KOH electrolyte at a current density of 10 A g-1. This study provides new insight into the design of high-performance activated carbon and new avenues for the application of coal-based carbon dots.

Lattice mismatch alleviation in p-CdTe/n-Si heterostructure by surface engineering on Si substrate.

The study used magnetron sputtering to investigate the growth of cadmium telluride (CdTe) thin films on surface treated n-type silicon (n-Si) substrates. The n-Si substrates were textured using potassium hydroxide (KOH) before the sputter deposition of CdTe. This was followed by cadmium chloride treatment to reduce the strain at the interface of CdTe and Si, which is caused by the incompatible lattice and thermal expansion mismatch (CTE). X-ray diffraction (XRD) analysis showed that the lowest FWHM and dislocation densities were obtained for CdCl2/CdTe/txt-nSi, which aligns with the scanning electron microscopy (SEM) results. In the SEM images, the interface bonding between the CdTe and Si surfaces was visible in the cross-sections, and the top-view images revealed sputtered CdTe thin films conforming to the patterns of pyramidal textured Si as an engineered surface to capture more light to maximize absorption in the CdTe/Si tandem design. The Energy dispersive X-ray (EDX) results showed that all the CdTe deposited on textured n-Si exhibited more Te atoms than Cd atoms, irrespective of the CdCl2 treatment. The presented results suggest that the texturization and CdCl2 treatment improved the morphology and grain boundary passivation of the sputtered CdTe. The adhesiveness of CdTe on the n-Si substrate was also significantly enhanced. Our findings further demonstrate that proper surface treatment of the Si substrate can greatly improve the quality of CdTe grown on Si by reducing the strain that occurs during the growth process. This study demonstrates a valuable method for enhancing the integration of CdTe with Si for two-junction tandem solar cell applications.

A Comparison Between Potassium Hydroxide (KOH) Microscopy and Culture for the Detection of Post-COVID-19 Rhino-Orbital-Cerebral Mucormycosis.

Background and objective Mucormycosis is an emerging and serious angioinvasive infection caused by filamentous fungi related to the order of Mucorales and the class of Mucormycetes. There was a marked increase in the number of cases of mucormycosis in India following the second wave of the coronavirus disease 2019 (COVID-19) pandemic in the year 2021. In this study, we aimed to compare potassium hydroxide (KOH) microscopy with culture for the detection of post-COVID-19 rhino-orbital-cerebral mucormycosis (ROCM). Materials and methods The KOH microscopy was performed with a 10% or 20% KOH-mounted slide with specimens collected from suspected cases of post-COVID-19 ROCM. Simultaneously, the culture was done on Sabouraud dextrose agar (SDA). These were incubated at 37 ℃ and 25 â„ƒ for 28 days. Diagnostic parameters were calculated by comparing KOH with gold standard culture. Results KOH mount was positive for broad aseptate fungal hyphae in 322 (54.1%) cases, while it was negative in 244 (41.0%) cases. KOH mount was positive for other fungi in 29 (4.8%) samples. The diagnostic accuracy of the KOH mount for Mucorales was 70.3%. KOH mount had a sensitivity of 84.9%, specificity of 61.5%, positive predictive value (PPV) of 56.9%, and negative predictive value (NPV) of 87.2%. Conclusions Based on our findings, the KOH microscopy positivity rate was higher in tissue samples compared to nasal swabs, with a sensitivity of 84.9%, specificity of 61.5%, PPV of 56.9%, and NPV of 87.2%. The overall diagnostic accuracy of the KOH mount for Mucorales was 70.3%.

Effective Use of Sugarcane-Bagasse-Derived KOH-Activated Biochar for Remediating Norfloxacin-Contaminated Water.

Bagasse-derived biochar (SCB750) was prepared at 750 °C using Chinese sugarcane bagasse as a carbon source and then modified with KOH for the removal of the antibiotic norfloxacin (NOR) from aqueous solutions. 3K-SCB750, prepared using a solid-to-liquid mass ratio of bagasse:KOH = 1:3, was found to have the best adsorption performance for NOR. Under the conditions of pH 5, 25 °C, 2.4 g L-1 adsorbent, and 300 mg L-1 NOR, its adsorption of NOR reached equilibrium (97.5% removal) after 60 min. The adsorption behaviours were in line with the quasi-second-order kinetic and Langmuir isotherm models, respectively. The maximum theoretical adsorption capacity reached up to 157.4 mg·g-1 at 40 °C. The thermodynamic parameters showed that the adsorption of NOR onto 3K-SCB750 was a spontaneous, endothermic, and physical process. In addition, Brunauer-Emmett-Teller analysis (BET), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and Raman spectroscopy were conducted to investigate the structural and adsorption properties of 3K-SCB750. Fourier transform infrared spectroscopy (FTIR) was also applied to understand the mechanism of adsorption of NOR onto 3K-SCB750. All of the results indicated that 3K-SCB750 had a large specific surface area of 1038.8 m2·g-1, an average pore size of 1.9 nm, and hierarchical structures with random pores and cracks for efficient removal of NOR. NOR adsorption mechanisms on 3K-SCB750 were related to the pore-filling effect and electrostatic attraction. Therefore, 3K-SCB750 biochar may be used as a promising adsorbent of antibiotics in wastewaters.

Hierarchical Porous Activated Carbon Derived from Coconut Shell for Ultrahigh-Performance Supercapacitors.

In this research, we successfully produced hierarchical porous activated carbon from biowaste employing one-step KOH activation and applied as ultrahigh-performance supercapacitor electrode materials. The coconut shell-derived activated carbon (CSAC) features a hierarchical porous structure in a honeycomb-like morphology, leading to a high specific surface area (2228 m2 g-1) as well as a significant pore volume (1.07 cm3 g-1). The initial test with the CSAC electrode, conducted in a 6 M KOH loaded symmetric supercapacitor, demonstrated an ultrahigh capacitance of 367 F g-1 at a current density of 0.2 A g-1 together with 92.09% retention after 10,000 cycles at 10 A g-1. More impressively, the zinc-ion hybrid supercapacitor using CSAC as a cathode achieves a high-rate capability (153 mAh g-1 at 0.2 A g-1 and 75 mAh g-1 at 10 A g-1), high energy density (134.9 Wh kg-1 at 175 W kg-1), as well as exceptional cycling stability (93.81% capacity retention after 10,000 cycles at 10 A g-1). Such work thus illuminates a new pathway for converting biowaste-derived carbons into materials for ultrahigh-performance energy storge applications.

Solving two environmental problems simultaneously：Microporous carbon derived from mixed plastic waste for CO2 capture.

Conversion of plastic waste into porous carbon for CO2 capture is an attractive approach to solve the carbon emission and plastic pollution problems, simultaneously. However, the previous studies are limited to the utilization of single PET plastic. The conversion of mixed plastic waste (MPW), which is of more practical significance, is seldom reported. In this study, mixed plastic waste was converted into porous carbon materials for CO2 capture through cascading autogenic pressure carbonization (APC) and chemical activation. The carbon yield of 56% was achieved through APC of MPW. The activator (KOH) dosage had significant effects on the structure and properties of the prepared porous carbons. Porous carbon prepared with KOH/C ratio of 4 had the largest micropore area and the maximum CO2 adsorption was 2.7 mmol g-1 at 298 K and 1 bar. The experimental data were well fitted to the pesudo first-order kinetic model. The MPW derived porous carbon exhibited not only high CO2 uptake capacity, but also fast adsorption rate, good selectivity of CO2 over N2 and good cyclic stability, which could be regarded as a promising adsorbent for CO2 adsorption.

Enhanced Assembling of N-and-K-Riched Macroalgae as Carbon Adsorbent for CO2 Capture with Ni(NO3)2/KOH as Co-Catalysts.

Porous-activated carbons have drawn great attention due to their important role in CO2 capture. Ni(NO3)2/KOH, as co-catalysts under different temperatures, were studied to obtain porous graphitized carbon from Sargassum horneri feedstock. The results indicated that the properties of the porous graphitized carbon generated at 850 °C were greatly enhanced, showing a large specific surface area of 1486.38 cm3·g-1 with narrowly distributed micropores (~0.67 nm) and abundant functional groups, which endowed high CO2 uptake; moreover, the high CO2 uptake was mainly attributed to the synergistic effect of Ni(NO3)2 and KOH, both in chemical modification and pore formation. The fitted values of the four kinetic models showed that the double exponential model provided the best description of carbon adsorption, indicating both physical and chemical adsorption. It is worth noting that carbon could be reused four times in the adsorption/desorption procedure in this research with good stability. This work focuses on the high-value-added comprehensive utilization of macroalgae, which not only is important for high-performance adsorbent preparation but also has positive benefits for the development and utilization of macroalgae resources.