High Total Pore Volume Research Articles

Fabrication of biocomposite materials with polycaprolactone and activated carbon extracted from agricultural waste

In this study, activated carbon was extracted from a source of agricultural waste (wheat straw) through a chemical activation process and blended with polycaprolactone (PCL) to fabricate new biocomposite materials. Three distinct types of activated carbon, designated as C1, C2, and C3 were obtained by varying the ratio of the activation agent and wheat straw and different drying conditions. Through a comprehensive array of analytical techniques, including FTIR, XRD, BET, EDS, and FE-SEM, we determined the optimal experimental method for extracting activated carbon from wheat straw and identified the most effective type of activated carbon (C3). Based on these analyses, C3 exhibits the highest carbon content, the greatest specific surface area (386.47 m2/g), and the highest total pore volume (0.2596 cm3/g). By blending polycaprolactone with the optimal activated carbon (at concentrations of 1, 3, and 5 wt%), biocomposite samples were fabricated. The results of FTIR indicate that the biocomposite materials containing 1, 3, and 5 wt% of activated carbon exhibit no disturbing peaks. However, the sample PCL-C,1 wt%, shows significant increases in the intensity of observed peaks. XRD analyses of the fabricated biocomposite samples illustrate that the sample containing 1 wt% of activated carbon has a greater tendency for crystallization compared to the other samples. Morphological analysis of the biocomposites and the dispersion of carbon particles within them demonstrate the least amount of agglomeration in the sample with an activated carbon concentration of 1 wt%. Upon assessing the mechanical properties of biocomposites, the same sample (1 wt% of C3) demonstrates more favorable characteristics than the other samples. Furthermore, a contact angle test was conducted to gauge the biocomposite hydrophilicity, revealing a 7 degree increase in contact angle for the sample with an activated carbon concentration of 1 wt% compared to the pure PCL sample. Thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC) were used to examine the weight loss, degradation temperature, melting temperature, and glass transition temperature of the synthesized materials. These analyses indicate a marginal augmentation in both melting and glass transition temperatures for the sample with an activated carbon concentration of 1 wt%.

Macroporous Poly(hydromethylsiloxane) Networks as Precursors to Hybrid Ceramics (Ceramers) for Deposition of Palladium Catalysts.

Poly(hydromethylsiloxane) (PHMS) was cross-linked with 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane (D4Vi) in water-in-oil High Internal Phase Emulsions to form macroporous materials known as polyHIPEs. It was shown that in the process of pyrolysis under Ar atmosphere at 520 °C, the obtained polyHIPEs were converted to ceramers with high yields (82.8-88.0 wt.%). Structurally, the obtained ceramers were hybrid ceramics, i.e., they consisted of Si-O framework and preserved organic moieties. Macropores present in the polyHIPE precursors remained in ceramers. Ceramers contained also micro- and mesopores which resulted from the precursor's mass loss during pyrolysis. Total pore volume and BET specific surface area related to the existence of micro- and mesopores in ceramers depended on the PHMS: D4Vi ratio applied in polyHIPE synthesis. The highest total pore volume (0.143 cm3/g) and specific surface area (344 m2/g) were reached after pyrolysis of the precursor prepared with the lowest amount of D4Vi as compared to PHMS. The composite materials obtained after deposition of PdO nanoparticles onto ceramers followed by reduction of PdO by H2 were active and selective catalysts for phenylacetylene hydrogenation to styrene.

Characterization and detailed mapping of C by spectral sensor for soils of the Western Plateau of São Paulo

Soil mineralogy and texture are directly related to soil carbon due to the physical properties of the clay surface. Traditional techniques for quantifying carbon in soil are time-consuming and expensive, making large-scale quantification for mapping unfeasible. The alternative is the use of soil sensors, such as diffuse reflectance spectroscopy (DRS), an economical, fast, and accurate technique for predicting carbon stocks. In this sense, this study aimed to (a) investigate the relationship of C with different soil mineralogical, chemical, and physical attributes for different geological and geomorphological compartments; (b) understand which spectral bands are most important for estimating C content; (c) estimate C content from diffuse reflectance spectroscopy using different mathematical techniques and indicate which one is the best for tropical soil conditions; and (d) map C contents in detail. The study area was the Western Plateau of São Paulo (WPSP), which covers approximately 13 million hectares (~ 48% of the State of São Paulo, Brazil). A total of 265 samples were collected in this area. The attributes clay, silt, sand, crystalline and non-crystalline iron, base saturation, soil density, total pore volume, total C, C stock, kaolinite/(kaolinite + gibbsite) and hematite/(hematite + goethite), hematite and goethite contents, and spectral curves were evaluated. The spectra were recorded at 0.5-nm intervals, with an integration time of 2.43 nm s−1 over the 350 to 2500-nm range (350–800 nm—visible—VIS and 801–2500 nm—near-infrared—NIR). The data were subjected to descriptive statistics, Spearman correlation, stepwise analysis, and cluster grouping for characterization purposes; partial least squares regression (PLSR) and random forest (RF) for estimation purposes; and geostatistics analysis for creation of spatial maps. Our results indicate that the highest C contents are associated with more clayey soils, oxidic mineralogy, higher total pore volume, and lower soil density in highly dissected basalt compartments. The random forest algorithm associated with the Vis–NIR spectral range is more efficient for estimating and mapping C contents. This suggests that integrating diffuse reflectance spectroscopy with machine learning techniques holds promise for shaping public policies related to land use, mitigating CO2 emissions, and facilitating the implementation of carbon credit policies in a rapid and economically efficient manner.

Potassium salts activated lignin-based biochar as an effective adsorbent for malachite green adsorption

Herein, a series of lignin-based porous carbons (LC) were prepared from sulfonated lignin through a simple and environmentally-friendly one-pot activated carbonization together with various potassium compounds as activators, and used for malachite green (MG) adsorption. The results showed that the prepared biochar, especially after K2CO3 activation, exhibited a honeycomb profile with large surface area (2107.6 m2/g) and high total pore volume (1.1591 cm3/g), having excellent efficiency for MG adsorption, and the biggest adsorption capacity was 2970.0 mg/g. The kinetic study together with thermodynamic analysis indicated that the adsorption of MG by LC-K2CO3 conformed to pseudo-second-order model and the adsorption process was spontaneous, feasible, and endothermic. Moreover, LC-K2CO3 also displayed good stability and selectivity, and can selective separate the cationic dye from binary-dye system. Furthermore, the adsorption mechanism proposed in this work manifested that the high-efficient MG adsorption by LC-K2CO3 was a result of multiple actions including hydrogen bonding, electrostatic attraction, π-π interaction and n-π interaction as well as physical absorption. The work not only provide a fundamental theory for dye removal from wastewater, but offered a new insight for lignin valorization.

Sustainable removal of tetracycline and paracetamol from water using magnetic activated carbon derived from pine fruit waste

This work presents highly porous magnetic activated carbon nanoparticles (MPFRC-A) derived from pine fruit residue. The MPFRC-A were produced through a three-step process: physical activation (carbonization temperature: 110–550 °C), chemical activation (H2SO4 (0.1 N, 96%)), and co-precipitation. These nanoparticles were then used to remove tetracycline (TC) and paracetamol (PC) from water. Functionalization with Fe3O4 nanoparticles on the surface of the pine fruit residue-derived activated carbon (PFRC-A) resulted in high saturation magnetization, allowing for separation from aqueous solution using an external magnet. The MPFRC-A adsorbent was characterized by Brunauer–Emmett–Teller (BET) analysis, Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), and Energy-dispersive X-ray spectroscopy (EDX) analyses, In the experimental section, the effects of various factors on the adsorption process were investigated, including pH, contact time, initial pollutant concentrations, adsorbent dosage, and temperature. Based on these investigations, adsorption isotherm models and kinetics were studied and determined. The results showed that MPFRC-A exhibited a large specific surface area (182.5 m2/g) and a high total pore volume (0.33 cm3/g). The maximum adsorption capacity was achieved at pH 6 and 5 for PC and TC drugs with an adsorbent dose of 400 mg and an initial concentration of 20 mg/L at 25 °C. The study revealed that the experimental data were well-fitted by the Langmuir isotherm model (R2 > 0.98), with maximum uptake capacities of 43.75 mg/g for TC and 41.7 mg/g for PC. Outcomes of the adsorption thermodynamics shows non-spontaneity of the reaction and the adsorption process by all adsorbents was endothermic.

Fabrication of Nanocellulose/Chitosan Nanocomposite Based on Loofah Sponge for Efficient Removal of Methylene Blue: Thermodynamic and Kinetic Investigations

AbstractWe established three nano-solid adsorbents: nanocellulose based on plant loofah sponge (NC), chitosan (CS), and nanocellulose/chitosan composite (CSC). These substances were employed as solid adsorbents to eliminate methylene blue (MB) dye from wastewater. Various characterization techniques were employed to investigate all the synthesized solid adsorbents, including TGA (thermogravimetric analysis), XRD (X-ray diffraction spectra), (BET) nitrogen gas adsorption-desorption, SEM (scanning electron microscope), TEM (transmission electron microscopy), FTIR (Fourier transform infrared) spectrometer, and zeta potential. According to our results, CSC showed greater thermal stability than LS and NC but lower than CS, mesoporous (2.012 nm), higher total pore volume (0.366 cm3. g− 1), specific surface area (639.3 m2. g− 1), and pHpzc of 7.22. The static adsorption of MB was well described by the Langmuir (R2 > 0.9872), Temkin (R2 > 0.9668), and Dubinin-Radushkevich (R2 > 0.9485) models. The composite of nanocellulose and chitosan exhibited the highest Langmuir adsorption capacity (301.20 mg. g− 1) at 47 °C after a 24 h shaking period at a dosage of 2 g. L− 1 as the adsorbent and pH of 7. The adsorption of MB by the fabricated solid materials fitted well with the linear PSO (R2 > 0.9806) and Elovich (R2 > 0.9574) kinetic model. The enthalpy, entropy, and free energy change for the adsorption of MB onto CSC were determined to be 47.11 kJ. mol− 1, 0.172 kJ. mol− 1. K− 1, and − 3.29 kJ. mol− 1, respectively at 20 °C. Thermodynamic investigation showed that MB adsorption is spontaneous, endothermic, favorable (0 < RL<1, 0.017–0.313), and physisorption (EDR < 8 kJ. mol− 1). Compared to the other eluents, nitric acid produced the highest desorption percentage (98.5%).

Dipole-induced hydrogen bonds enhanced P/O co-doped Lyocell-based porous carbon fiber cloth for hydrogen storage under ambient pressure

Currently, the hydrogen storage application of carbon-based adsorbent materials is mostly implemented under the pressure conditions of 30–300 bar, while there is few targeted studies conducted on the unsaturated adsorption under ambient pressure conditions. Therefore, based on industrialized Lyocell biopolymer fiber precursors and the enhancement effects of dipole-induced hydrogen bonds (DIHB), this work presents a facile construction strategy for P/O co-doped Lyocell-based porous carbon fiber cloth (Ly-ACF-F40). By the technical route of thermal stabilization---sonication assisted phosphoric acid activation---hydrogen bonds introduced by interfacial fluorination, the constructed Ly-ACF-F40 acquires a high specific surface area (1870 m2/g) and total pore volume (1.277 cm3/g), and an excellent hydrogen storage capacity of 3.22 wt% under ambient pressure conditions (77 K, 1 bar). The study directly demonstrated in the experiment that dipole induced hydrogen bonding H(I)-H(II)···F can effectively enhance the atmospheric hydrogen storage density on the basis of other eliminating influencing factors of specific surface area. The simple construction strategy of porous carbon-based materials can provide reference for the research of unsaturated adsorption hydrogen storage materials under ambient pressure conditions, also assist in the application and promotion of low-cost solid hydrogen storage materials.

Unpredicted porosity improvement upon thermal reactivation of a fouled multi-walled carbon nanotube

Deposition of carbonaceous species on a solid catalyst’s surface during a catalysed processes is quite usual. This causes fouling, or depletion of the textural features, with a performance decay. In this work, preliminary results for an ex situ thermal oxidative reactivation of a fouled MWCNT are presented. The coke is nearly completely removed and, as a side effect, some of the MWCNT is combusted. Remarkably, the textural features are improved; 23 % higher BET area and 29 % higher total pore volume, while maintaining the isotherm shape. These improvements are attributed to two factors. Firstly, the removal during reactivation of non-porous (or less-porous) carbon domains present in the starting MWCNT, that positively influences the porosity in various ways; a control experiment employing the fresh MWCNT strongly suggests this hypothesis. Secondly, the new microporosity also contributes to the better BET.

Single-Component Adsorption Equilibria of CO2, CH4, Water, and Acetone on Tapered Porous Carbon Molecular Sieves.

Engineered carbon molecular sieves (CMSs) with tapered pores, high surface area, and high total pore volume were investigated for their CO2, CH4, water, and acetone adsorption properties at 288.15, 298.15, 308.15 K, and pressures of <1 bar. The results were compared with BPL carbon. The samples exhibited higher adsorption capacity for CO2 compared to BPL carbon, with Carboxen 1005 being the highest due to the presence of ultramicropores (pores smaller than 0.8 nm). Similar observations were made for CH4 except at 288.15 K. Although the CMSs exhibited higher hydrophobicity than BPL carbon, the latter had the highest acetone uptake for all investigated temperatures due to its higher oxygen content, which facilitates stronger interactions with polar VOC molecules. Heats of adsorption were calculated using the Clausius-Clapeyron equation after fitting the isotherms with the dual-site Langmuir-Freundlich model, and results largely corroborated the order of adsorption capacities of CO2, CH4, and water on the carbon materials.

Thermochemical energy storage performances of Co3O4-based honeycombs with multi-scale composite pores

Metal oxide redox system characterized open-loop operation, high energy density, and high reversibility, which is one of the most promising thermochemical energy storage technologies for the next-generation concentrated solar power plants. Most of the previous studies focused on the material properties, while the energy storage performance of oxide monolithic bodies, such as energy storage density and heat storage/release rate, has rarely been reported. In this paper, a novel and effective method for the improvement of the energy storage performance of oxide honeycombs with multi-scale composite pores is proposed and presented. Methyl cellulose and four common biomass materials, including bagasse, loofah, juniper leaf, and pine needle, were used as pore-forming agents for oxide honeycombs. The pyrolysis of methyl cellulose forms small-scale pores in the honeycomb bodies and contributes the major pore volume. The biomass templates further optimize the pore characteristics, all biomass-templated Co3O4-based honeycomb bodies have higher total pore volume and permeability than that of biomass-free honeycomb body. The honeycomb with 2.5 wt% pine needle achieves the highest energy storage density, with an average of 694.62 kJ/kg during the second to fifteenth cycles. In addition, the honeycomb containing 7.5 wt% pine needle has the highest energy store/release rate. Biomass-templated Co3O4-based honeycomb shows a high crushing strength, and there are no obvious cracks and structural deformations on its surface after 15 thermal cycles. The findings demonstrate that the methyl cellulose and biomass template method can effectively optimize the pore structure and energy storage properties of the oxide honeycombs, thereby expanding the application prospects of Co3O4-based honeycombs in thermochemical energy storage.

Lignin-derived nitrogen doped hierarchical porous carbon spheres for highly efficient dichloromethane adsorption

Biomass-prepared porous carbon materials are promising solid adsorbents for the removal of volatile organic compounds (VOCs). However, their application is hindered due to the insufficient number of pores and poor surface activity. In this study, a lignin-derived nitrogen-doped hierarchical porous carbon sphere (NHPCS-0.5) with abundant surface active sites was synthesised through spray drying and carbonisation–activation methods. The optimised NHPCS-0.5 displayed a high BET specific surface area (2961 m2·g−1) and total pore volume (1.57 cm3·g−1), developed hierarchical porous distribution with micro-/meso-/macropores and satisfactory surface nitrogen content. Moreover, it exhibited an excellent dichloromethane adsorption capacity of 156 mg·g−1 and maintained 86% of initial capacity after five regeneration cycles, indicating an outstanding regenerative ability. The nitrogen introduction improved the micropore volume and adsorption capacity. Adsorption mechanism reveals that micropore filling and enhanced van der Waals interaction of carbon surface with dichloromethane molecule by N-containing functional groups played a vital role in adsorption, and mesopores contributed to the high adsorption rates. The above results indicate the potential of NHPCS-0.5 as an adsorbent for VOC removal and provide new ideas for the utilisation of lignin and design of carbon sphere materials.

Conversion of waste cork to N-doped porous carbons by urea-assisted hydrothermal method for enhanced VOC capture

Converting waste resources into porous carbon for pollutants capture is an effective strategy to achieve the environmental goal of “treating waste with waste”. Cork is an ideal precursor of porous carbons due to its ordered honeycomb-like cell structure and layered composition distribution. Herein, N-doped porous carbons (PCs) were prepared via two steps of urea-assisted hydrothermal carbonization and chemical activation to mitigate volatile organic compounds (VOCs) pollution. Results indicated that the obtained PC4-800 exhibited remarkable features for adsorption including high total pore volume (0.97 cm3/g) and specific surface area (1864.89 m2/g), as well as abundant N-containing functional groups. The excellent pore structure was primarily owing to the corrosion of the carbon matrix by the gas produced from the reaction of K2CO3 and N-containing functional groups. The adsorption results showed that the PC4-800 have an outstanding toluene adsorption capacity (867.03 mg/g) that outperforming majority of adsorbents previously reported. There are substantial pores in N-doped PCs with a pore width of 1.71–2.28 nm, which is 3 to 4 times the molecular dynamic diameter of toluene, and plays a crucial role in the absorption process. Moreover, the promotional influence of N-functional groups on the toluene adsorption process was verified through DFT calculation by Gaussian imitating, where N-6 generated π-electron enrichment sites on the surface of N-doped PCs, facilitating π-π dispersion with the benzene ring in toluene. This study provides a new strategy to convert waste cork into high-performance adsorbents for VOCs removal.

Green synthesis of Kenaf-based activated carbons with excellent rate capability and cycle-life via hydrothermal-co-activation process for high-performance capacitive energy storage

The invention of high-performance electrode materials through a simple and green approach is always important for energy storage applications. Herein, we have prepared highly porous activated carbons (ACs) from biomass kenaf (KF) by hydrothermal and steam activation methods. A number of optimization experiments, such as hydrothermal pre-treatment (100, 150 and 200 °C), steam activation temperature (600, 700, 800, and 900 °C) and time of steam flow (15, 30, 60 and 90 min) were performed to control the specific surface area, micro- and/or meso-pores, total pore volume for an excellent electrochemical performance. The as-obtained porous ACs exhibited a high specific surface area (∼1733 m2/g) with high total pore volume (∼0.916 cm3/g) and high mesopore volume (∼28.4%), which are beneficial for the excellent double layer formation over the surface of activated electrode and also provide transport channel for an effective diffusion of electrolyte ions. The as-derived ACs were used as electrode materials for the fabrication of symmetric supercapacitor device in 6 M KOH. The fabricated device exhibited a high energy density of 4.86 Wh kg−1 at power density of 2500 W kg−1 with outstanding stability (∼96.3%) over 10,000 charge-discharge cycles.

Influence of Co3O4 Nanostructure Morphology on the Catalytic Degradation of p-Nitrophenol.

The design and fabrication of nanomaterials with controllable morphology and size is of critical importance to achieve excellent catalytic performance in heterogeneous catalysis. In this work, cobalt oxide (Co3O4) nanostructures with different morphologies (nanoplates, microflowers, nanorods and nanocubes) were successfully constructed in order to establish the morphology-property-performance relationship of the catalysts. The morphology and structure of the nanostructured Co3O4 were characterized by various techniques, and the catalytic performance of the as-prepared nanostructures was studied by monitoring the reduction of p-nitrophenol to p-aminophenol in the presence of excess NaBH4. The catalytic performance was found to be strongly dependent on their morphologies. The experimental results show that the pseudo-first-order reaction rate constants for Co3O4 nanostructures with various shapes are, respectively, 1.49 min-1 (nanoplates), 1.40 min-1 (microflowers), 0.78 min-1 (nanorods) and 0.23 min-1 (nanocubes). The Co3O4 nanoplates exhibited the highest catalytic activity among the four nanostructures, due to their largest specific surface area, relatively high total pore volume, best redox properties and abundance of defect sites. The established correlation between morphology, property and catalytic performance in this work will offer valuable insight into the design and application of nanostructured Co3O4 as a potential non-noble metal catalyst for p-nitrophenol reduction.

Creating high-affinity binding sites for efficient CO2 and iodine vapor uptake through direct synthesis of novel triazine-based covalent organic polymers

Two types of triazine-based covalent organic polymers were successfully constructed through a one-pot and catalyst-free polycondensation approach. More specifically, two kinds of aromatic aldehyde containing different hydroxyl content named terephthalaldehyde and 2, 4, 6-trihydroxyisophthalaldehyde were selected and the derived polymers (denoted as POPs-1 and POPs-2) with large Brunauer-Emmett-Teller (BET) surface areas (> 360 m2/g), high total pore volume (> 0.47 m3/g), good stability and different heteroatoms (such as N and O) contents were prepared. Interestingly, POPs-1 featuring high BET surface area and N content (up to 34.83 %) exhibited excellent iodine vapor uptake of 441 wt% at 348 K/1.0 bar, POPs-2 with high O content (up to 25.83 %) showed better CO2 adsorption capacity (91.8 mg/g) at 273 K/1.0 bar and higher isosteric heat of adsorption (up to 85.0 kJ/mol) than that of POPs-1. This value of the isosteric heat is the highest value reported to date for porous organic polymers. This excellent adsorption performance was resulted either from the large BET surface area or high heteroatoms (N and O) contents of the porous adsorbents. The study offer an alternative route to develop high-performance porous adsorbents to capture carbon dioxide and iodine.

High-efficient removal and adsorption mechanism of organic dyes in wastewater by KOH-activated biochar from phenol-formaldehyde resin modified wood

The treatment of wastewater contaminated with organic dyes has become an intricate challenge in water pollution control. Currently, sophisticated chemical modifications and synthetic methods are frequently needed to enhance the adsorption capacity of biochar for removing dyes during the treatment process. In order to develop a facile, low-cost and efficient biochar absorbent, an activated biochar (KOH/PF-WB) was successfully synthesized from phenol-formaldehyde (PF) resin modified wood via pyrolysis and potassium hydroxide (KOH) activation. Based on the joint effect of PF resin and wood, KOH/PF-WB-700–2 exhibited a remarkable porous structure and abundant oxygen-containing functional groups, which resulted in a substantially high specific surface area (SBET = 2301.61 m2/g) and total pore volume (Vtotal = 1.205 cm3/g). Additionally, the PF resin modification led to increased disorder and more defect sites of activated wood biochar. As a result, KOH/PF-WB-700–2 demonstrated superior adsorption capacity for congo red (3472.22 mg/g) and methylene blue (1112.35 mg/g) dyes compared to some reported adsorbents. The adsorption process could be better described by the pseudo-second-order kinetic model and Langmuir isotherm model, while the overall process was spontaneous and feasible. The primary adsorption mechanism involved pore filling through the modulation of PF resin, along with the cooperative effects of electrostatic attraction, hydrogen bonding and π-π interaction. This finding provides a viable strategy for the waste PF-modified wood cyclic application, and offer technical support for the prospect of KOH/PF-WB for the removal of organic dyes.

From grape bagasse to graphene-like porous carbon nanosheets for CO2 capture.

Graphene-based materials have increasingly attracted attention in recent years. It is a material is recognized worldwide due to its numerous applications in several sectors. However, graphene production involves several challenges: scalability, high costs, and high-quality production. This study synthesized graphene-like porous carbon nanosheets (GPCNs) through a thermochemical process under a nitrogen atmosphere using grape bagasse as a precursor. Three temperatures (700, 800, and 900 ºC) of the pyrolysis process were studied. Chemical graphitization and activation were used to form high-specific surface area materials: FeCl3.6H2O(aq) and ZnCl2(s) in a simultaneous activation-graphitization (SAG) method. The materials obtained (GPCN700, GPCN800, and GPCN900) were compared to previously produced chars (C700, C800, and C900). A high specific surface area and total pore volume were obtained for GPCN materials, and GPCN900 presented the highest values: 1062.7 m2g-1 and 0.635 cm3g-1, respectively. The GPCN and char materials were classified as mesoporous and applied as adsorbents for CO2(g). The GPCN800 presented the best CO2(g) adsorbent, with a CO2(g) adsorption capacity of 168.71mgg-1.

Remediation of pesticides contaminated water using biowastes-derived carbon rich biochar

The competition impact and feedstock type on the removal of water pesticides using biochar have not yet been sufficiently investigated. Therefore, here we investigated the potentiality of three different biochars (BCs) derived from rice husk (RHB), date pit (DPB), and sugarcane bagasse (SBB) biowastes for the simultaneous removal of ten pesticides from water in a competitive adsorption system. The BCs structural characterization and morphology were investigated by XRD, FTIR spectroscopy and SEM analysis. The potential adsorption mechanisms have been investigated using various isothermal and kinetic models. RHB showed the highest removal percentages (61% for atrazine/dimethoate and 97.6% for diuron/chlorfenvinphos) followed by DPB (56% for atrazine/dimethoate and 95.4% for diuron/chlorpyrifos) and then SBB (60.8% for atrazine/dimethoate and 90.8% for chlorpyrifos/malathion). The higher adsorption capacity of RHB and DPB than SBB can be due to their high total pore volume and specific surface area (SSA). Langmuir model described well the sorption data (R2 = 0.99). Adsorption equilibrium was achieved after 60 min for RHB, and 120 min for both DPB and SBB. The optimum adsorbent dose (g/L) was 10 for RHB and 4 for DPB and SBB. The removal efficiency of pesticides was enhanced by decreasing pH from 9 to 5 by RHB and to 3 by DPB and SBB. XRD and FTIR spectroscopy confirmed that BCs contain some active adsorption groups and metal oxides such as MgO, SiO, Al2O3, CaO, and TiO2 that can play an effective role in the pesticides sorption. BET-N2 adsorption analysis demonstrated that the BC pore size contributes significantly to pesticide adsorption. These findings indicate that RHB, DPB, and SBB have ability for adsorption of water pesticides even under acidic conditions. Therefore, the rice husk, date pit, and sugarcane bagasse biowastes could be pyrolyzed and reused as effective and low-cost sorbents for elimination of hazardous substances such as pesticides in the aqueous environments.

Hierarchical porous carbon with tunable apertures and nitrogen/oxygen heteroatoms for efficient adsorption and separation of VOCs

Porous carbon materials are good adsorbent candidates for removing volatile organic compounds (VOCs) due to their reliability and cost-effectiveness. Especially, the pore size distribution (PSD) of porous carbon materials plays a critical role in VOCs adsorption and separation. In this study, we present benzimidazole-derived porous carbons (BICs) with controllable pore size and oxygen/nitrogen heteroatoms. The pore size is controlled by adjusting the reaction degree of inorganic salt (K2CO3) and nitrogen-containing groups in the system. The tunable pore size distribution makes BICs highly efficient for the adsorption and separation of VOCs. BIC-3-900 exhibits a dominant pore size distribution of 3.0–4.0 nm and an exceptionally high total pore volume of 2.42 cm3/g, leading to ultra-high adsorption capacities for benzene and methanol (22.19 and 52.65 mmol/g, respectively) at 293 K. In addition, BIC-1-700 dominated by the micropore size is more favorable for adsorbing low-concentration small molecule VOCs (with a dynamic adsorption capacity of 4.21 mmol/g for methanol at 3800 ppm). In terms of the adsorptive separation performance, BIC-1-900 has an efficient benzene/methanol selectivity (∼30.13) due to its PSD (1.2–2.0 nm) which was more favorable for capturing low-concentration benzene. Moreover, both experimental and simulation (GCMC and DFT) results demonstrate that the abundant N/O heteroatoms doping in BIC-1-700 results in charge heterogeneity and stronger electrostatic affinity for polar VOCs molecules. Herein, our findings suggest that BICs with controllable pore size and oxygen/nitrogen heteroatoms have significant potential in practical VOCs capture and separation.

Effect of the Structure of Highly Porous Silica Extracted from Sugarcane Bagasse Fly Ash on Aflatoxin B1 Adsorption.

Sugarcane bagasse fly ash is industrial waste produced by incinerating biomass to generate power and steam. The fly ash contains SiO2 and Al2O3, which can be used to prepare aluminosilicate. This latter material exhibits high potential as an adsorbent in various applications, including the livestock industry where issues related to contamination of aflatoxins in animal feeds need to be addressed; addition of adsorbents can help decrease the concentration of aflatoxins during feed digestion. In this study, the effect of the structure of silica prepared from sugarcane bagasse fly ash on physicochemical properties and aflatoxin B1 (AFB1) adsorption capability compared with that of bentonite was investigated. BPS-5, Xerogel-5, MCM-41, and SBA-15 mesoporous silica supports were synthesized using sodium silicate hydrate (Na2SiO3) from sugarcane bagasse fly ash as a silica source. BPS-5, Xerogel-5, MCM-41, and SBA-15 exhibited amorphous structures, while sodium silicate possessed a crystalline structure. BPS-5 possessed larger pore size, pore volume, and pore size distribution with a bimodal mesoporous structure, while Xerogel-5 exhibited lower pore size and pore size distribution with a unimodal mesoporous structure. BPS-5 with a negatively charged surface exhibited the highest AFB1 adsorption capability compared with other porous silica. However, the AFB1 adsorption capability of bentonite was superior to those of all porous silica. Sufficient pore diameter with high total pore volume as well as high intensity of acid sites and negative charge on the surface of the adsorbent is required to increase AFB1 adsorption in the in vitro gastrointestinal tract of animals.