Solid-phase microextraction using a ß-ketoenamine-linked covalent organic framework coating for efficient enrichment of synthetic musks in water samples.

Covalent organic frameworks with tunable porous crystallinity and outstanding stability have recently exhibited fascinating pretreatment performance as solid-phase microextraction coatings. In this report, a ß-ketoenamine-linked covalent organic framework (TpPa-1) was successfully constructed through a Schiff-base-type reaction between 1,3,5-triformylphloroglucinol (Tp) and para-phenylenediamine (Pa-1). A TpPa-1 coating was then fabricated on a stainless-steel fiber for capturing trace synthetic musks. This TpPa-1 coating exhibited strong interaction with synthetic musks because of its hydrophobicity and π-π affinity. This TpPa-1-based solid-phase microextraction methodology, coupled with gas chromatography-tandem mass spectrometry, provided high enrichment factors (1214-12 487), wide linearity (0.5-1000 ng L-1), low limits of detection (0.04-0.31 ng L-1), and acceptable reproducibility (relative standard deviation, <10%) for nine synthetic musks. Recoveries at three spiked levels in three types of water samples were between 76.2% and 118.7%. These results indicated the promising applicability of the TpPa-1 as a solid-phase microextraction fiber coating for reliably detecting trace concentrations of synthetic musks in the environment.

Nitrogen-rich covalent organic frameworks as solid-phase extraction adsorbents for separation and enrichment of four disinfection by-products in drinking water.

Disinfection by-products (DBPs) in drinking water can pose a health risk to humans. In this work, a new nitrogen-rich covalent organic frameworks (TpTt-COFs) was synthesized and applied firstly as a novel solid-phase extraction (SPE) trapping media for four ultra-trace levels of DBPs in drinking water samples. Under the optimal conditions, these DBPs were absorbed on a SPE cartridge; then, the DBPs were eluted with the optimized volume of eluent. The concentrated elution was detected and quantified by gas chromatography-mass spectrometry. Low limits of detection (0.0004-0.0063 ng mL-1), wide linearity (0.002-50 µg L-1), good reproducibility (1.54-2.88%) and repeatability (1.28-3.40%) were obtained. This novel method has been successfully applied to the analysis of ultra-trace levels DBPs in real drinking water samples. These accurate experimental results by this method indicated that the novel TpTt-COFs as a SPE trapping material was an attractive option for efficient and effective analysis of ultra-trace levels DBPs in future.

Kinetic, thermodynamic and isotherm investigations of Cu2+ and Zn2+ adsorption on LiAl hydrotalcite-like compound.

LiAl hydrotalcite-like compound (LiAl HTlc) was synthesized via a hydrothermal method and used to adsorb Cu2+ and Zn2+ for investigating the adsorption characteristics of heavy metal cations. The X-Raydiffraction (XRD), fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM) and transmission electron microscopy (TEM) characterizations revealed the interconnecting flower-like layered structure of LiAl HTlc. The adsorption kinetics and isotherms of Cu2+ and Zn2+ on LiAl HTlc agreed with the pseudo-second-order model and the Langmuir model at a given sorbent concentration (Cs), respectively. The Cs-effect on the adsorption kinetics and isotherms was observed, and the Langmuir-surface component activity (SCA) equation could be utilized to characterize the effect of Cs in the adsorption isotherms. The adsorption process was spontaneous and endothermic. The adsorption mechanism denoted that the adsorption process was controlled using two main mechanisms, i.e., surface complexation and isomorphic substitution. This is the first report, to the best of our knowledge, on the usage of LiAl HTlc for the removal of heavy metal cations Cu2+ and Zn2+ from a solution. LiAl HTlc is a promising sorbent for treating water containing heavy metal cations.

Development of dispersive solid-phase extraction with polyphenylene conjugated microporous polymers for sensitive determination of phenoxycarboxylic acids in environmental water samples.

High-performance capturing polar phenoxycarboxylic acids herbicides (PCAs) from water samples remains a great challenge because PCAs form salt easily and dissolve. Polyphenylene-based conjugated microporous polymers (PP-CMPs), a fascinating type of polymers, bear π-conjugation over 3D polyphenylene scaffolds, inherent micropore, and large surface area, which are essential for capturing trace PCAs in complex samples. This work developed a novel approach to quantify trace PCAs using PP-CMPs as an efficient dispersive solid-phase extraction (d-SPE) adsorbent. The developed method based on PP-CMPs achieved high sensitivity with limits of detection of 0.55-3.84 ng L-1, satisfactory correlation coefficients (≥ 0.9912), good linearity (50-10,000 ng L-1), and good precisions (2.0-9.0%). Moreover, this method was used for simultaneous monitoring of the amounts of five PCAs in environmental water samples with satisfactory spiked recoveries (86.9-101.3%). All these fact demonstrated that this new d-SPE technique based on PP-CMPs exhibited a promising potential for highly sensitive analysis of trace PCAs in complex samples.

Using bamboo charcoal as solid-phase extraction adsorbent for the ultratrace-level determination of perfluorooctanoic acid in water samples by high-performance liquid chromatography-mass spectrometry.

In recent years, bamboo charcoal, a new kind of material with special microporous and biological characteristics, has attracted great attention in many application fields. In this paper, the potential of bamboo charcoal to act as a solid-phase extraction (SPE) adsorbent for the enrichment of the environmental pollutant perfluorooctanoic acid, which is one of the newest types of persistent organic pollutants in the environment, has been investigated. Important factors that may influence the enrichment efficiency--such as the eluent and its volume, the flow rate of the sample, the pH of the sample and the sample volume--were investigated and optimized in detail. Under the optimum conditions, the limit of detection for PFOA was 0.2 ng L(-1). The experimental results indicated that this approach gives good linearity (R(2) = 0.9995) over the range 1-1000 ng L(-1) and good reproducibility, with a relative standard deviation of 4.0% (n = 5). The proposed method has been applied to the analysis of real water samples, and satisfactory results were obtained. The average spiked recoveries were in the range 79.5-118.3%. All of the results indicate that the proposed method could be used for the determination of PFOA at ultratrace levels in water samples.