Adsorption of Hydrogen Sulfide (H2S) from Municipal Solid Waste by Using Biochars

The emission of hydrogen sulfide (H2S) from municipal solid waste is one of the environmental issues that raised the public’s attention and awareness. Exposure to H2S that brings a foul smell of rotten eggs will cause headaches, irritation, dizziness, fatigue, and even death if the concentration of H2S is too high. The study’s goals are to investigate the properties of biochars made from rice hulls, banana peels, and sawdust; to compare the biochars’ physical and chemical properties; and establish the H2S removal efficiency of the three biochars. Biochars derived from rice hull (RHB-500), banana peel (BPB-550), and sawdust (SDB-500) by pyrolysis were used as the adsorbents. The biochar yield, pH, ash content, surface functional group, and morphology of the biochars produced were investigated. In this study, H2S was synthesized by mixing food waste and soil in the experimental column. The H2S produced was reduced by the adsorption method. The removal efficiencies of H2S for each biochar were determined by allowing the synthetic H2S to flow through the two columns that were packed with sand (act as control) and biochars, respectively. All biochars were alkaline, and BPB-550 had the highest pH, followed by SDB-500 and finally RHB-500. The order for removal efficiency of H2S (>94%) is BPB-550 > SDB-500 > RHB-500. Overall, the biochars derived from biomass had a strong ability to act as the adsorbents for H2S removal.

Covalent Functionalization of Nickel Phosphide Nanocrystals with Aryl-Diazonium Salts

Covalent functionalization of Ni2P nanocrystals was demonstrated using aryl-diazonium salts. Spontaneous adsorption of aryl functional groups was observed, with surface coverages ranging from 20-96% depending on the native reactivity of the salt as determined by the aryl substitution pattern. Increased coverage was possible for low reactivity species using a sacrificial reductant. Functionalization was confirmed using thermogravimetric analysis, FTIR and X-ray photoelectron spectroscopy. The structure and energetics of this nanocrystal electrocatalyst system, as a function of ligand coverage, was explored with density functional theory calculations. The Hammett parameter of the surface functional group was found to linearly correlate with the change in Ni and P core-electron binding energies and the nanocrystal’s experimentally and computationally determined work-function. The electrocatalytic activity and stability of the functionalized nanocrystals for hydrogen evolution were also improved when compared to the unfunctionalized material, but a simple trend based on electrostatics was not evident. Density functional theory was used to understand this discrepancy, revealing that H adsorption energies on the covalently functionalized Ni2P also do not follow the electrostatic trend and are predictive descriptors of the experimental results.

Covalent Functionalization of Nickel Phosphide Nanocrystals with Aryl-Diazonium Salts

Covalent functionalization of Ni2P nanocrystals was demonstrated using aryl-diazonium salts. Spontaneous adsorption of aryl functional groups was observed, with surface coverages ranging from 20-96% depending on the native reactivity of the salt as determined by the aryl substitution pattern. Increased coverage was possible for low reactivity species using a sacrificial reductant. Functionalization was confirmed using thermogravimetric analysis, FTIR and X-ray photoelectron spectroscopy. The structure and energetics of this nanocrystal electrocatalyst system, as a function of ligand coverage, was explored with density functional theory calculations. The Hammett parameter of the surface functional group was found to linearly correlate with the change in Ni and P core-electron binding energies and the nanocrystal’s experimentally and computationally determined work-function. The electrocatalytic activity and stability of the functionalized nanocrystals for hydrogen evolution were also improved when compared to the unfunctionalized material, but a simple trend based on electrostatics was not evident. We used density functional theory to understand this discrepancy and found that H adsorption energies on the covalently functionalized Ni2P also do not follow the electrostatic trend and are predictive descriptors of the experimental results.

First-in-Class Phosphorus Dendritic Framework, a Wide Surface Functional Group Palette Bringing Noteworthy Anti-Cancer and Anti-Tuberculosis Activities: What Lessons to Learn?

Based on phenotypic screening, the major advantages of phosphorus dendrimers and dendrons as drugs allowed the discovery of new therapeutic applications, for instance, as anti-cancer and anti-tuberculosis agents. These biological activities depend on the nature of the chemical groups (neutral or cationic) on their surface as well as their generation. As lessons to learn, in the oncology domain, the increase in the generation of metallo-dendrimers is in the same direction as the anti-proliferative activities, in contrast to the development of polycationic dendrimers, where the most potent anti-tuberculosis phosphorus dendrimer was observed to have the lowest generation (G0). The examples presented in this original analysis of phosphorus dendrimers and dendrons provide support for the lessons learned and for the development of new nanoparticles in nanomedicine.

Effect of activation temperature on properties of H3PO4-activated carbon

The effects of different activation temperatures (Ta), ranging from 300 to 750 °C, on the ash content, yield, ignition point, microcrystalline structure, surface functional group, pore structure, and adsorption performance of activated carbon in preparing activated carbon by phosphoric acid (H3PO4) were systematically studied. The yield and volatile content of activated carbon decreased with the increase of Ta, while the ash content, ignition point, and graphitization degree showed the opposite results. The turning point of ash content increasing rate of activated carbon occurred at 500 °C. The thermal decomposition temperature of phosphonate compounds was approximately 450 °C. With increased Ta, micropores were generated first, followed by mesopores. The ignition point of activated carbon was related to the volatile content and the degree of graphitization. Activated carbon with low ash content, high yield, well-developed pore structure and good adsorption performance was prepared at 350 to 425 °C. With increased Ta, the volatile content decreased, and the ignition point of activated carbon increased. At Ta higher than 500 °C, the aromatic and condensed ring structure, graphitization degree, and mesopore ratio of the activated carbon increased, yielding decreased adsorption performance.

Identification of Surface Functional Group on Activated Carbon from Waste Sago

Activated carbon is a powerful adsorption material which mainly used as pollutants adsorption. The adsorption properties own derived from the main functional groups or chemical atoms derived from the activation processes. In this study, the activated carbon was prepared from waste sago and activated using two different chemicals activation agents called phosphoric acid and potassium hydroxide. The aim of this study was to identify the surface functional group on waste sago activated carbon produced. The results showed that activated carbon with phosphoric acid activator contained OH, C=C, CO and CH functional groups, while activated carbon with potassium hydroxide activator contained O-H, C≡C, C=C, C-O and C-H functional groups. These results lead to support the recommendations for the development of the application of waste sago activated carbon made as adsorbents in the purification of lead (II) and cadmium (II) wastewater.

Adsorption of ammonium, nitrite, and nitrate onto rice husk biochar for nitrogen removal

This study aims to investigate the adsorption capacity of ammonium NH4+, nitrite NO2- and nitrate NO3- onto rice husk biochar (RHB) obtained from 550 °C pyrolysis temperature in the context of using low-cost absorbent for recirculating aquaculture system (RAS). Raw RHB at its original size 5–8 mm has been choosen for testing its adsorption capacity as well as several key material properties (pHPZC, surface area, and elemental analysis). From surface functional group analysis, there existed the O–H group (at frequency 3443 cm-1), –CH3 (2360 cm-1), and either –C=O or C=C group (in the range of frequency 1600–1650 cm-1) as well as –COOH (1456 cm‒1) that helped enhance chemical adsorption. The experimental adsorption data has been roughly consistent with Langmuir and Freundlich models that used to calculate the maximum saturated monolayer adsorption capacity Q0max of ammonium, nitrite, and nitrate were 0.1003, 0.2477, and 0.1290 mg/g respectively. Therefore, RHB could be a potential candidate for biofilter application in both targets cost-efficient and sustainable that worth applied at scale.