본 연구는 해조류인 괭생이 모자반을 탄화하여 만든 바이오차의 중금속 흡착 및 제거 효과를 확인하고 중금속 흡착제로 이용 가능성을 확인하고자 연구가 수행되었다. 모자반 바이오차(SBC)는 500℃조건에서 2시간 열분해를 통해 생산하였다. 중금속 흡착실험은 Pb, Cd, Cu 및 Zn의 각 농도별 흡착량을 확인하였으며, Freundlich 및 Langmuir 등온흡착모델을 통해 중금속 흡착 효율성을 확인하였다. 모자반 바이오차의 중금속 제거효율은 Pb, Cd, Cu 및 Zn에서 각각 97.3, 85.2, 76.4 및 42.0%로 Pb＞Cd＞Cu＞Zn 순의 제거효율을 보였다. 등온흡착결과로 Freundlich 등온흡착패턴은 L형이었으며, 흡착강도(1/n)는 0.49 ~ 0.80 범위로 조사되었다. Langmuir 등온흡착식에서 최대흡착량은 Pb, Cd, Cu 및 Zn에서 각각 200, 92.6, 47.8 및 70.4 mg g-1이었으며, 흡착강도는 각각 0.4950, 0.1004, 0.0245 및 0.0188로 조사되었다. 본 실험 결과로 볼 때 모자반 바이오차는 중금속 흡착제로써 활용이 가능할 것으로 보여지며, 이를 활용하기 위한 추가 연구가 필요하다고 보여진다.

In this paper, the adsorption removal characteristic for 10 species of perfluoroalkyl and polyfluoroalkyl substances (PFAS) was investigated using GAC and modified GAC (GAC-Cu). After modification with Cu(II), the amount of copper was to 1.93 and 4.73 mg/g for GAC and GAC-Cu, respectively. The total amount of 10 species of PFAS per specific area was obtained to 0.548 and 0.612 ng/m2 for GAC and GAC-Cu, respectively. A series of batch test confirmed lower efficiency was observed with a smaller number of carbon chain length and the removal efficiency of PFCA (perfluoroalkyl carboxylic acids) was lower than that of PFSA (perfluoroalkyl sulfonic acids) with the same carbon chain length. Regarding the pH effect, the adsorption capacity was decreased with increase of pH due to the increase of electrostatic repulsion. According to pseudo first and second order (PFO and PSO) kinetic models, while the values of equilibrium uptake and time did not show significant difference, a difference in uptake was observed between 24-48h. Furthermore, based on correlation analysis, Log Kow and uptake have a high correlation with molecular weight (M.W.) and initial concentration, respectively. These results show that long-chain PFAS have higher removal efficiency due to their increased hydrophobicity.

Moso bamboo, as a kind of renewable functional material, exhibits outstanding development potential. It is promising to prepare activated carbon with good mechanical strength and high specific surface area using moso bamboo as raw material. In this work, we employed a hydraulic extruder to extrude the bamboo charcoal and the adhesive to obtain the moso bamboo activated carbon, and improved the specific surface area of the columnar activated carbon through high-temperature water vapor activation. Through the catalytic role of the water vapor activation process, the formation and expansion of the pores were promoted and the internal pores were greatly increased. The obtained columnar activated carbon shows excellent mechanical strength (93%) and high specific surface area (791.54 m2/ g). Polyacrylamide@asphalt is one of the most effective adhesives in the high-temperature water vapor activation. The average pore size (22.99 nm) and pore volume (0.36 cm3/ g) of the prepared columnar activated carbon showed a high mesoporous ratio (83%). Based on the excellent pore structure brought by the activation process, the adsorption capacity of iodine (1135.75 mg/g), methylene blue (230 mg/g) and carbon tetrachloride (64.03 mg/g) were greatly improved. The resultant moso bamboo columnar activated carbon with high specific surface area, excellent mechanical properties, and outstanding adsorption capacity possesses a wide range of industrial applications and environmental protection potential.

In this paper, the formation and characterization of Pt2, Pt3 as well as Pt4 atomic clusters in cup-stacked carbon nanotubes (CSCNTs) are evaluated by DFT to examine the adsorption capacity under the clusters. The results show that the Pt clusters move toward the bottom edge or form rings in the optimized stable structure. Pt far from the carbon substrate possesses more active electrons and adsorption advantages. The three clusters can adsorb up to 17, 18, and 16 hydrogen molecules. Loading metal clusters at the bottom edge maintains a relatively good adsorption property despite the low binding energy through comparative studies. The adsorption capacity does not increase with the number of Pt for metal aggregation reducing the hydrogen adsorption area thus impacting the hydrogen storage ability and the aggregation phenomenon limiting the action of Pt metal. During adsorption, chemisorption occurs only in the Pt2 cluster, while multiple hydrogen molecules achieve physiochemical adsorption in the Pt3 and Pt4 clusters. Compared with the atomic loading of the dispersion system in equal quantities, the dispersion system features higher molecular stability and can significantly reduce the energy of the carbon substrates, providing more sites for hydrogen adsorption in space.

In the present study, a novel pH-sensitive hydrogel composite of pectin-grafted-poly (acrylic acid-co-itaconic acid)/MWCNTs- COOH was prepared by using graft copolymerization of acrylic acid and itaconic acid on pectin backbone with incorporation of MWCNTS- COOH. The prepared hydrogel composite has been employed for the adsorption and controlled release of the diclofenac sodium (DS) drug. The hydrogel composite was characterized by the analysis methods: FTIR, XRD, SEM, and TGA to analyze structural characteristics before and after DS drug adsorption. The swelling ratio of the hydrogel composite was investigated at different pH values from pH 1.2 to 10. According to the results, the swelling ratio of the hydrogel composite was found 4195% at pH 7.4. Adsorption process parameters such as pH, contact time, adsorbent dose, and temperature were investigated and found to have a significant influence on DS drug adsorption. The maximum DS drug loading through adsorption of 91% was obtained at pH 3, adsorbent dose of 0.05 g, contact time of 150 min, and temperature of 15 °C. The adsorption isotherm and kinetic results were well-fitted to Freundlich and second-order models. Thermodynamic parameters including changes in Gibb’s free energy, enthalpy, and entropy suggested that the adsorption of DS drug onto hydrogel composite was a spontaneous and exothermic process. The in vitro drug release experiment showed that the cumulative release of DS drug from hydrogel composite after 35 h was significantly higher in simulated intestinal fluid at pH 7.4 than in simulated gastric fluid at pH 1.2.

Exploring highly efficient, and low-cost oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) catalysts is extremely vital for the commercial application of advanced energy storage and conversion devices. Herein, a series of graphene-like C2N supported TMx@C2N, (TM = Fe, Co, Ni, and Cu, x = 1, 2) single- and dual-atom catalysts are designed. Their catalytic performance is systematically evaluated by means of spin-polarized density functional theory (DFT) computations coupled with hydrogen electrode model. Regulating metal atom and pairs can widely tune the catalytic performance. The most promising ORR/OER bifunctional activity can be realized on Cu2@ C2N with lowest overpotential of 0.46 and 0.38 V for ORR and OER, respectively. Ni2@ C2N and Ni@C2N can also exhibit good bifunctional activity through effectively balancing the adsorption strength of intermediates. The correlation of reaction overpotential with adsorption free energy is well established to track the activity and reveal the activity origin, indicating that catalytic activity is intrinsically governed by the adsorption strength of reaction intermediates. The key to achieve high catalytic activity is to effectively balance the adsorption of multiple reactive intermediates by means of the synergetic effect of suitably screened bimetal atoms. Our results also demonstrate that lattice strain can effectively regulate the adsorption free energies of reaction intermediates, regarding it as an efficient strategy to tune ORR/OER activity. This study could provide a significant guidance for the discovery and design of highly active noble-metal-free carbon-based ORR/OER catalysts.

This paper aims to review the odor removal performance and operating parameters of pilot and full-scale chemical scrubbers, bioscrubbers, biofilters, and biotrickling filters for odor control in wastewater treatment plants. Based on the performance of full-scale facilities installed in wastewater treatment plants, empty-bed residence times were the shortest for bioscrubbers (7.5±2.5s), followed by chemical scrubbers (20±8.1s), biotrickling filters (22.2±26.2s), and biofilters (48±30s). The removal efficiencies of complex odors by biofilters, biotrickling filters, bioscrubbers, and chemical scrubbers were 97.7±1.9%, 87.7±15.6%, 89.0±9.0%, and 70.0%, respectively. The investment cost was the lowest for biofilters, followed by biotrickling filters, bioscrubbers, and chemical scrubbers. In addition, the operating costs of these deodorization technologies were in the following order: biofilters < bioscrubbers and biotrickling filters < chemical scrubbers. However, most studies on odor control for wastewater treatment processes have been conducted on a laboratory scale with model odors (single odorous compound or mixtures of 2-3 odorous compounds). Therefore, field research to develop deodorization technologies for wastewater treatment plants should be more actively conducted to accumulate data for the design and operation of full-scale deodorizing systems.

Graphene-modified melamine sponges (RGO-MSs) were prepared, as adsorbents with photothermal conversion ability, utilizing solar energy to achieve heavy oil temperature rise, viscosity reduction, and efficient adsorption recovery of highly viscous oil. The RGO-MSs were prepared through a simple impregnation method. The photothermal performance and heavy oil adsorption performances of RGO-MSs with different densities and thicknesses were observed. It was found that as the density increases, the thermal conductivity of RGO-MS increases too, leading to the increase of the average oil absorption rate. The reduction of thickness is beneficial to improving of the adsorption rate. The prepared RGO-MS with a density of 21.5 mg/cm−3 and a height of 1 cm (RGO-MS-3-1) shows excellent mechanical properties and fatigue resistance. Cyclic adsorption–desorption of RGO-MS-3-1 was achieved through extrusion/ ethanol washing. After 10 cycles of reuse through extrusion, the adsorption capacity decreased from 52.90 to 50.02 g g− 1, with a loss of 5.4%. The material was then washed with petroleum ether and ethanol in turn. Its adsorption capacity can restored to 98.8% of the initial value, showing a promising application prospect on heavy oil leakage treatment. The easily prepared RGO-MS exhibits excellent light absorption and photothermal oil adsorption properties, providing a good solution for the problem of heavy oil leakage at sea.

This study proposes the use of a cobalt-based Prussian blue analogue (Co-PBA; potassium cobalt hexacyanoferrate), as an adsorbent for the cost-effective recovery of aqueous ammonium ions. The characterization of Co-PBA involved various techniques, including Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, nitrogen adsorption-desorption analysis, and zeta potential. The prepared Co-PBA reached an adsorption equilibrium for ammonium ions within approximately 480 min, which involved both surface adsorption and subsequent diffusion into the interior. The isotherm experiment revealed a maximum adsorption capacity of 37.29 mg/g, with the Langmuir model indicating a predominance of chemical monolayer adsorption. Furthermore, the material consistently demonstrated adsorption efficiency across a range of pH conditions. Notably, adsorption was observed even when competing cations were present. Co-PBA emerges as a readily synthesized adsorbent, underscoring its efficacy in ammonium removal and selectivity toward ammonium.

In this study, Pitch-derived activated carbon (PAC) pellets were by steam activation for automotive carbon canisters. The crystal structure of PAC was analyzed using X-ray diffraction. The textural properties of PAC were studied by Brunauer– Emmett–Teller (BET), Horvath-Kawazoe (HK), and Non-Localized Density Functional Theory (NLDFT) equations with N2/ 77 K isotherm adsorption/ desorption curves. The butane adsorption capacity of the PAC pellets was analyzed according to the ASTM D5228 standard. With increasing steam activation time, the specific surface area and total pore volume of the PAC increased 650–1950 m2/ g and 0.27–1.02 cm3/ g, respectively. The mesopore ratio of PAC increased with increasing activation time and was observed up to 28.4% at 190 min. The butane adsorption capacity of the PAC increased and was observed to range from 10.86 to 51.55%. A close relationship between butane adsorption capacity and pore size (1.47–2.39 nm) was found. Finally, the butane activity of PAC was found to be 51.55% for the steam activated at 950 ℃ for 190 min; this butane activity is 24% better than that of the coconut-derived activated carbon (41.43%) with a similar specific surface area, indicating that pitch is a suitable material for the activated carbon of automotive carbon canisters.

Thin films of yttria-stabilized zirconia (YSZ) nanoparticles were prepared using a low-temperature deposition and crystallization process involving successive ionic layer adsorption and reaction (SILAR) or SILAR-Air spray Plus (SILAR-A+) methods, coupled with hydrothermal (175 °C) and furnace (500 °C) post-annealing. The annealed YSZ films resulted in crystalline products, and their phases of monoclinic, tetragonal, and cubic were categorized through X-ray diffraction analysis. The morphologies of the as-prepared films, fabricated by SILAR and SILAR-A+ processes, including hydrothermal dehydration and annealing, were characterized by the degree of surface cracking using scanning electron microscopy images. Additionally, the thicknesses of the YSZ thin films were compared by removing diffusion layers such as spectator anions and water accumulated during the air spray plus process. Crack-free YSZ thin films were successfully fabricated on glass substrates using the SILAR-A+ method, followed by hydrothermal and furnace annealing, making them suitable for application in solid oxide fuel cells.

Cellulose has experienced a renaissance as a precursor for carbon fibers (CFs). However, cellulose possesses intrinsic challenges as precursor substrate such as typically low carbon yield. This study examines the interplay of strategies to increase the carbonization yield of (ligno-) cellulosic fibers manufactured via a coagulation process. Using Design of Experiments, this article assesses the individual and combined effects of diammonium hydrogen phosphate (DAP), lignin, and CO2 activation on the carbonization yield and properties of cellulose-based carbon fibers. Synergistic effects are identified using the response surface methodology. This paper evidences that DAP and lignin could affect cellulose pyrolysis positively in terms of carbonization yield. Nevertheless, DAP and lignin do not have an additive effect on increasing the yield. In fact, combined DAP and lignin can affect negatively the carbonization yield within a certain composition range. Further, the thermogravimetric CO2 adsorption of the respective CFs was measured, showing relatively high values (ca. 2 mmol/g) at unsaturated pressure conditions. The CFs were microporous materials with potential applications in gas separation membranes and CO2 storage systems.