Development of Nickel Oxide-Functionalized Biosilica for N-DBPs Extraction

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Comprehensive vocabulary flashcards covering the chemical, analytical, and environmental concepts related to the development and application of functionalized biosilica sorbents for swimming pool water monitoring.

Last updated 7:53 PM on 8/16/26
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20 Terms

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Nitrogenous Disinfection By-Products (N-DBPs)

A class of contaminants including haloacetonitriles and halonitromethanes produced when chlorine disinfectants react with nitrogen-containing matter such as sweat, urine, and cosmetics in swimming pool water.

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Nitrogen Paradox

The toxicological observation that N-DBPs represent over 50% of total genotoxicity in pool water despite accounting for only 5% of the total disinfection by-product mass.

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Biosilica

An eco-friendly source of commercially available silica derived from agricultural waste, such as maize cob ash, valued for its high surface area and tunable pore structure.

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Nickel Oxide (NiO)

A p-type semiconductor and functional material with high surface reactivity and affinity for nitrogen-containing compounds used to enhance the adsorption performance of biosilica.

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Dispersive Solid-Phase Extraction (d-SPE)

A sample preparation technique where micro-amounts of sorbent are dispersed directly into a sample to achieve high enrichment factors and reduce solvent consumption.

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Point of Zero Charge (PZC)

The pH value at which a material's surface carries no net electric charge, which for NiO typically ranges from 7.3 to 10.7.

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Lewis Acid Coordination

A selective binding mechanism involving orbital overlap between electron-deficient Ni2+ sites on a sorbent and lone pair electrons on nitrogen atoms in N-DBP molecules.

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Debye Screening Length

The distance over which electrostatic interactions occur; in high-salinity pool water, this length is compressed, which can inhibit long-range electrostatic adsorption.

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Wet Impregnation

A synthesis technique for preparing functionalized sorbents by loading metal precursors onto a silicate support, followed by aging, drying, and calcination at specific temperatures.

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Quenching

The process of deactivating residual disinfectants, such as chlorine, using agents like ascorbic acid to prevent analyte degradation or the formation of chemical artifacts.

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Haloacetonitriles (HANs)

Highly toxic and reactive nitrogenous by-products characterized by an instability at pH > 7.0 and high cytotoxicity due to their cyano groups.

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Matrix Effect

The analytical challenge caused by high concentrations of dissolved organic carbon (DOC) and total dissolved solids (TDS) that interfere with analyte identification and cause signal suppression in mass spectrometry.

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AGREEprep

A green analytical metric framework used to assess the environmental sustainability of sample preparation procedures based on factors like solvent consumption and waste generation.

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Self-Cleaning Mechanism

The ability of a sorbent surface to mineralize organic matter through advanced oxidation processes involving hydroxyl and superoxide radicals, potentially regenerating active adsorption sites.

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Pseudo-Second-Order Model

A kinetic model used to simulate the rate of analyte uptake, assuming that chemisorption involving electron sharing is the rate-limiting step.

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Intraparticle Diffusion Model

A three-stage mass transfer model that describes how analytes move through the bulk phase and films before penetrating the internal pores of a nanostructured sorbent.

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Enrichment Factor (EF)

The ratio of the analyte concentration in the final eluate to the initial analyte concentration in the sample, representing the effectiveness of the preconcentration step.

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Scherrer Equation

A mathematical relationship, D=Kλβcos(θ)D = \frac{K\lambda}{\beta \cos(\theta)}, used to calculate the mean crystallite size of nanoparticles based on X-ray diffraction peak broadening.

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Langmuir Isotherm Model

An adsorption model that assumes monolayer adsorption onto a finite number of identical surface sites, expressed as qe=qmaxKLCe1+KLCeq_e = \frac{q_{max}K_L C_e}{1 + K_L C_e}.

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ICH Q2(R2)

The International Council for Harmonisation requirement used for validating analytical procedures, covering parameters such as linearity, LOD, LOQ, and precision.