Bamboo-derived adsorbents for environmental remediation: A review of recent progress.

The bamboo family of plants is one of the fastest-growing species in the world. As such, there is an abundance of bamboo residues available for exploitation, especially in southeast Asian, central African and south American regions. The preparation of efficient adsorbents from bamboo residues is an emerging exploitation pathway. Biochars, activated carbons or raw bamboo fibers embedded with nanoparticles, each class of materials has been shown to be highly efficient in adsorption processes. This review aims to summarize recent findings in the application of bamboo-based adsorbents in the removal of organic, inorganic, or gaseous pollutants. Therefore, this review first discusses the preparation methods and surface modification methodologies and their effects on the adsorbent elemental content and other basic properties. The following sections assess the recent progress in the adsorption of heavy metals, organics, and gaseous substances by bamboo-based adsorbents, focusing on the optimum adsorption capacities, adsorption mechanisms and the optimum-fitting kinetic models and isotherms. Finally, research gaps were identified and directions for future research are proposed.

Low-cost novel nano-constructed granite composites for removal of hazardous Terasil dye from wastewater.

The hazardous dyes on mixing with water resources are affecting many life forms. Granite stone is popular worldwide for decorating floors, making other forms of decorative materials and items. Granite stone powder waste can be obtained free of cost from marble factories as factories spend on the disposal of this waste. In the present study, novel granite stone powder waste composite has been prepared and utilized for the effective removal of Terasil dye. Two types of granite including gray granite and white granite were used in pure, calcinized, and chemically modified forms. Freundlich adsorption isotherm model best explained the adsorption mechanism of dye removal using granite composites as compared to other adsorption isothermal models. Characterization techniques like scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy were used for the determination of morphological features and functional groups of granite composites. The obtained results were statistically analyzed using analysis of variance (ANOVA) along with the post hoc Tukey test. An extraordinarily high Terasil dye uptake capacity (more than 400 mg/g) was exhibited by granite composites prepared using sodium metasilicate. The synthesized novel nano-constructed composites provided a viable strategy as compared to the pure granite stone for dye removal from wastewater water.

Glycerol-Based Retrievable Heterogeneous Catalysts for Single-Pot Esterification of Palm Fatty Acid Distillate to Biodiesel.

The by-product of the previous transesterification, glycerol was utilised as an acid catalyst precursor for biodiesel production. The crude glycerol was treated through the sulfonation method with sulfuric acid and chlorosulfonic acid in a reflux batch reactor giving solid glycerol-SO3H and glycerol-ClSO3H, respectively. The synthesised acidic glycerol catalysts were characterised by various analytical techniques such as thermalgravimetric analyser (TGA), infrared spectroscopy, surface properties adsorption-desorption by nitrogen gas, ammonia-temperature programmed desorption (NH3-TPD), X-ray diffraction spectroscopy (XRD), elemental composition analysis by energy dispersive spectrometer (EDX) and surface micrographic morphologies by field emission electron microscope (FESEM). Both glycerol-SO3H and glycerol-ClSO3H samples exhibited mesoporous structures with a low surface area of 8.85 mm2/g and 4.71 mm2/g, respectively, supported by the microscopic image of blockage pores. However, the acidity strength for both catalysts was recorded at 3.43 mmol/g and 3.96 mmol/g, which is sufficient for catalysing PFAD biodiesel at the highest yield. The catalytic esterification was optimised at 96.7% and 98.2% with 3 wt.% of catalyst loading, 18:1 of methanol-PFAD molar ratio, 120 °C, and 4 h of reaction. Catalyst reusability was sustained up to 3 reaction cycles due to catalyst deactivation, and the insight investigation of spent catalysts was also performed.

The investigation of activated carbon by K2CO3 activation: Micropores- and macropores-dominated structure.

In this study, the K2CO3 activation of bamboo was investigated in detail, and the structure and properties of the prepared activated carbons were tested for the feasibility of CO2 capture application and the potential for both ion and bacteria adsorption for use in the field of hazardous wastewater treatment. Activated carbons were produced with different activator ratios, from 0.5 to 6 according to the sample mass ratio. The ratio of H or O to C (H/C or O/C) increased with the increasing amount of K2CO3 added for the activation. The samples had a highly-porous microporous structure, in which the micropore volume was calculated to be 0.6 cm3 g-1 by the DR method of the CO2 adsorption isotherm at 298 K. The BET surface area and total pore volume estimated from the N2 adsorption isotherms at 77 K of the activated materials increased according to the increase of the K2CO3 impregnation ratio to a maximum value of 1802 m2 g-1 and 0.91 cm3 g-1, respectively. Moreover, the K2CO3-activated samples had a specific morphology, that is, macropores which are presumed to be derived from bubbles. The X-ray-CT images showed that the bubble-like structure is not only on the surface but also inside the samples. The results of gas adsorption methods, mercury porosimetry, and SEM showed the co-existence of micropores (<2 nm) and macropores (100-10,000 nm). The results highlighted the unique pore structure, that is, the coexistence of micropores and macropores that would contribute to forming solutions for carbon sequestration in the atmosphere and wastewater treatment.

Potential heterogeneous nano-catalyst via integrating hydrothermal carbonization for biodiesel production using waste cooking oil.

Hydrothermal carbonization (HTC) provides alternatives technique to produce a nanosize activated carbon from biomass with a high surface area. Herein, this study we prepared empty fruit bunch-based activated carbon (EFBHAC) using HTC technique. The activated carbon was then functionalized with K2CO3 and Cu(NO3)2 to produce bifunctional nano-catalyst for simultaneous esterification-transesterification of waste cooking oil (WCO). The physicochemical properties were performed i.e. N2 sorptions analysis, TPD-CO2/NH3, FESEM, EDX, FTIR and XRD analysis. The results revealed that produced EFBHAC possessed a BET surface area of 4056.17 m2 g-1, with pore volume of 0.827 cm3 g-1 and 5.42 nm of pore diameter resulting from hydrolysis, dehydration decarboxylation, aromatization and re-condensation during HTC process. Impregnation of EFBHAC with K2CO3 and Cu(NO3)2 granted a high amount of basicity and acidity of 9.21 mmol g-1 and 31.41 mmol g-1, respectively, accountable to high biodiesel yield of 97.1%, produced at the optimum condition of 5 wt% of catalyst loading, 12:1 of methanol to oil molar ratio at 70 °C for 2 h. More than 80% of biodiesel was produced after the 5th cycle depicted the good reusability. The transformations from WCO to biodiesel was confirmed via 1H NMR, FTIR and TGA analysis. Fuel properties revealed kinematic viscosity of 3.3 mm2 s-1, cetane number of 51, flash point of 160.5 °C, cloud and pour point of 11 °C and -3 °C, respectively. These results show the excellent potential of waste materials to prepare bifunctional nano-catalysts to produce higher biodiesel yield which has potential to be commercialized.

Thermal induced changes of rice straw phytolith in relation to arsenic release: A perspective of rice straw arsenic under open burning.

On-site open burning is a common practice for handling rice straw, but its negative impacts, e.g., biomass loss and air pollution, are largely debated worldwide. To address the negative effects of open burning, many efforts have been made to 'ignite' worldwide bans. However, these bans are likely based on a singular view in which some positive aspects of open burning are overlooked. In this study, we aimed to determine the thermal-induced changes of straw and straw arsenic (As) under open burning and heat-treatments (in the temperature range from 300 to 900 °C). It was found that silica phase in rice straw (so-called phytolith) can encapsulate As in its structure. Open burning or heat-treatment of straw resulted in a tighter association of As and phytolith, thereby reducing dissolution of As. We proposed an opinion that open burning causes air pollution, but it can increase the activity of phytolith in sequestrating As, enabling delayed As cycle in rice ecosystems. The combat of on-site open burning of rice straw to reduce air pollution will alter straw handling routines, thereby changing the cycle of straw phytolith and the route of straw As.

Conversion of Waste Polyethylene Terephthalate (PET) Polymer into Activated Carbon and Its Feasibility to Produce Green Fuel.

In this study, a novel idea was proposed to convert the polyethylene terephthalate (PET) waste drinking-water bottles into activated carbon (AC) to use for waste cooking oil (WCO) and palm fatty acid distillate (PFAD) feasibility to convert into esters. The acidic and basic char were prepared by using the waste PET bottles. The physiochemical properties were determined by employing various analytical techniques, such as field emission scanning electron microscopy (FESEM), thermogravimetric analysis (TGA), Fourier transform infrared (FTIR), Brunauer-Emmett-Teller (BET) and temperature-programmed desorption - ammonia/carbon dioxide (TPD-NH3/CO2). The prepared PET H3PO4 and PET KOH showed the higher surface area, thus illustrating that the surface of both materials has enough space for impregnation of foreign precursors. The TPD-NH3 and TPD-CO2 results depicted that PET H3PO4 is found to have higher acidity, i.e., 18.17 mmolg-1, due to the attachment of phosponyl groups to it during pretreatment, whereas, in the case of PET KOH, the basicity increases to 13.49 mmolg-1. The conversion results show that prepared materials can be used as a support for an acidic and basic catalyst for the conversion of WCO and PFAD into green fuel.

Evolution of physico-chemical properties of Dicranopteris linearis-derived activated carbon under various physical activation atmospheres.

This work emphasizes the effect of the physical activation using CO2 and steam agents on the physicochemical properties of activated carbon produced from Dicranopteris linearis (D. linearis), a fern species widely distributed across tropic and subtropic ecoregions. The D. linearis-derived chars produced under pyrolysis at 400 °C for 1 h were activated in various CO2-steam proportions. As revealed by the IR and Raman spectra, the structure of the activated chars was heavily dependent on the relative proportion of CO2 and steam. The total specific surface area (SSA) of the activated chars proportionally increased with the increase in steam proportion and was comparable to the values of commercial activated char products. Specifically, the activation under CO2- and steam-saturated conditions has correspondingly resulted in SSA increasing from 89 to 653 m2g-1 and from 89 to 1015 m2g-1. Steam also enhanced the development of mesoporous structures of the D. linearis-derived char products, thereby extending their potential applications, particularly for industries that require high rigidity in the product such as pharmaceutical and cosmetic sectors.

Fungicide application can intensify clay aggregation and exacerbate copper accumulation in citrus soils.

Fungicide application for controlling fungal diseases can increase copper (Cu) accumulation in soil. More urgently, Cu released from fungicides can associate with soil clay and favour the mutual aggregation of Cu and soil clay, thereby potentially intensifying the accumulation of Cu. We investigated the effects of Cu salt and six common Cu-based fungicides on colloidal dynamics of a clay fraction from citrus cultivated soil. Batch experiments were carried out to provide the loading capacity of the clay fraction for Cu. The colloidal dynamic experiments were performed over a pH range from 3 to 8 following a test tube method, while surface charge, the key electrochemical factor of the solid-liquid interface, was quantified by a particle charge detector. It was found that all the studied fungicides, via releasing Cu2+, acted to effectively favour clay aggregation. The dissolved organic matter obtained from the dissolution of polymers in fungicides can theoretically stimulate clay dispersion. However, their effects were obscured due to the overwhelming effect of Cu2+. Therefore, Cu2+ appears as the most active agent in the fungicides that intensifies clay aggregation. These findings imply that the intensive application of fungicides for plant protection purposes can inadvertently reduce clay mobility, favour the co-aggregation of clay and fungicides, and hence potentially exacerbate the contamination of the citrus soil.

CO2 activation of bamboo residue after hydrothermal treatment and performance as an EDLC electrode.

CO2 activation of the solid residue of bamboo after hydrothermal treatment, which is used for the production of xylo-oligosaccharide, was investigated in detail. The reference temperature for carbonization and CO2 activation was 800 °C. The activated carbon from a solid residue was demonstrated to have a higher potential for making EDLC electrodes than bamboo activated carbon thanks to its very low ash content (almost 0) and high porosity structure with a BET surface area up to ca. 2150 m2 g-1. The electrochemical performance of ELDC electrodes prepared from solid residue-derived activated carbon in 1 M H2SO4 aqueous solution was measured and well compared with carbon from bamboo. Through investigation, it is clear that the capacitance of the electrode made from the solid residue has a better capacity than that of raw bamboo.

Carbonization and H3PO4 activation of fern Dicranopteris linearis and electrochemical properties for electric double layer capacitor electrode.

Today, the world's climate change is a growing problem, plant carbon sequestration is one of the effective ways to mitigate climate change by reducing greenhouse gases, mostly carbon gases. Dicranopteris linearis (D. linearis), a common fern species in the tropic or subtropic ecoregions, has been recently recognized as a potential feedstock to produce highly porous biochar. This study aims to enhance the specific surface area (SSA) and pore volumes of biochars derived from the D. linearis by H3PO4 activation and examine electrical properties of the activated biochars and their possible usage for the electric double-layer capacitor (EDLC) electrode. The treated raw fern was activated with H3PO4 85% by the three different mixing ratios 1:0, 1:1, and 1:3 (w/w) and then pyrolysis under N2 flow maintained at 500 °C for 1 h. The performance as the electrode for an EDLC was evaluated in 1 mol L-1 H2SO4 solution for the H3PO4-activated samples. The SSA and pore volumes were drastically increased after activation. The maximum SSA and pore volume were 1212 m2 g-1 and 1.43 cm3 g-1, respectively for the biochar activated at 400 °C with a weight mixing ratio 1:3 (w/w) between the fern and H3PO4 acid while these values of the biochar at 400 °C were 12 m2 g-1 and 0.02 cm3 g-1, respectively. The biochar activated at 600 °C with the mixing ratio 1:1 (w/w) showed the maximum capacitance value, ca. 108 F g-1 at 1 mV s-1. The activation using H3PO4 showed a positive tendency to enhance electrochemical properties and it could be a premise toward a higher performance of EDLC from the D. linearis derived activated biochar.

Direct Synthesis of Graphene Layer Covered Micro Channel on Diamond Surface Using Ni Wire.

In order to propose a new simple method for the fabrication of a microchannel covered with a graphene layer on a diamond substrate, the application of a phase transition via a solid solution phenomenon, that is, the dissolution of a thermodynamic-metastable phase and the deposition of a thermodynamic-stable phase, was performed in this study. A CVD diamond film in contact with a Ni wire (100 micrometers in diameter) was heated under flowing H2. The experimental results in this study proved that a micro-channel (ca. 5 micrometers deep) covered with a graphene layer, the stacking number of which was more than 6, can be successfully patterned on a diamond substrate. The etching rate was estimated to be ca. 1.3-1.4 µm h-1. It was proved based on the experimental data from this study that this method can be used to fabricate a microreactor on a diamond substrate although the technique may be refined.

Partial Delignification as Pretreatment for Nanoporous Carbon Material from Biomass.

For the pretreatment in order to nano prepare porous carbon from biomass such as bamboo, a mixture of acetic acid and hydrogen peroxide was used for the partial delignification of bamboo. The pretreatment should be effective for the removal of lignin because the lignin percentage after the pretreatment depended on the treatment time and the treatment temperature. For the concentration of the mixture used for the pretreatment in this study, a small amount of lignin (ca. 2 wt%) remained even after a sufficiently-long treatment time. The BET specific surface area of the carbon material prepared by the heat treatment at 800 degrees C for 1 h under flowing N2 was related to the pretreatment conditions, and the specific surface areas of the samples were found to be related to the lignin percentage. The removal of lignin while maintaining the microstructure derived from plant tissue could be the reason for the local maximum of the specific surface area at ca. 5% of the lignin.

Attempt of Deposition of Ag-Doped Amorphous Carbon Film by Ag-Cathode DC Plasma with CH4 Flow.

A simple DC plasma apparatus having large Ag cathode with CH4 flow was used for the attempt to prepare Ag-doped amorphous carbon film. As the gaseous source, CH4 and the additive (N2 or Ar) were used for the plasma process. When N2 was the additive, the substrate surfaces after the plasma process were electrical conductor although high electrical resistance. The growth rate of the deposits decreased with increasing the amount of N2, and the deposits contained nitrogen. Although the small amount of silver was detected by XPS, the peak for Ag may not be in the carbon deposit but be in interlayer formed at Ar etching process. When Ar was the additive, the substrate surfaces after the plasma process were also electrical conductor although high electrical resistance. The growth rate of the deposits was almost independent of the amount of Ar, and the deposits contained no argon. The small XPS peaks for Ag may not be in the carbon deposit but be in interlayer formed at Ar etching process. Both the prepared samples had high antibiotic property. The method of this study could be used for the surface reforming with amorphous carbon coating having electrical conductivity and antibiotic property.

Improvement of electrical conductivity while maintaining a high-transmittance of graphene oxide/MWCNT film by hydrazine reduction.

In this study, we attempted to synthesize a transparent electrode with a composite of along graphene with multi-walled carbon nanotubes (MWCNT). Hydrazine was used for the reduction process. After the treatment with hydrazine, the sheet resistance was reduced from over 10 Momega/sq. The longest dip time sample (reduced GO/MWCNT-5, RGO/MWCNT-5) had the lowest sheet resistance (114 komega/sq). The reason for this decrease is likely due to the fact that the concentration of MWCNT in the deposited film increased with increases in the deposition time based on the higher density of the MWCNT. Although the transmittance decreased with decreases in the sheet resistance, the transmittances of all the samples were approximately 80% at 550 nm. We succeed in synthesizing a film that maintains transmittance (80%) despite a decreasing sheet resistance.

Improvement of visible light photocatalytic acetaldehyde decomposition of bismuth vanadate/silica nanocomposites by cocatalyst loading.

Photocatalytic activity of bismuth vanadate (BiVO(4)) for acetaldehyde decomposition under visible light irradiation was improved by inclusion of a nanocomposition of silica as an adsorbent material and loading of platinum (Pt) or trivalent iron ion (Fe(3+)) as reduction cocatalysts. Addition of silica enhanced photocatalytic activity due to improvement of adsorption ability, but total decomposition of acetaldehyde was not observed within 24h of visible light irradiation. For further improvement of photocatalytic activity, BiVO(4) with an optimized amount of silica composition were modified with Pt or Fe(3+). Photodeposition of Pt greatly increased photocatalytic activity, and acetaldehyde was totally decomposed within 24h of visible light irradiation.

Photochemical modification of diamond powders with elemental sulfur and their surface-attachment behavior on gold surfaces.

A useful method of modifying the surface of diamond powder with sulfur-containing functionalities was developed by the photolysis of elemental sulfur. The introduction of sulfur-containing functional groups on the diamond surfaces was confirmed by X-ray photoelectron spectroscopy (XPS), diffuse reflectance Fourier transform infrared spectroscopy (DRIFT) and mass spectroscopy analyses. The sulfur-modified diamond powder attached to gold surfaces through sulfur-containing linkages. In brief, the exposure of the modified diamond powder to a gold colloid resulted in gold nanoparticles being attached to the diamond powder. The treatment of the modified diamond powder with thin gold film on a Si substrate resulted in the alignment of surface-attached diamond powder through sulfur linkages formed by self-assembly.