Applied Water Science. Группа авторов

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colspan="9"> SBSE DMP, DEP, DBP, BBP, DEHP, and DNOP Sea and esturiane waters (20 mL plus 30% w/v NaCl and 20% v/v MeOH) SBSE using a PDMS stir bar, stirring at room temperature for 60–200 min, and thermal desorption at 300°C for 10 min GC-MS 0.0003–0.063 μg/L 95–124% at 0.1 μg/L One river water sample and 2 estuarian water samples were analyzed and contained all PAEs at levels from 0.0036 ± 0.0004 to 1.314 ± 0.018 μg/L A Plackett–Burman and 2 central composite designs were used for optimization purposes. 6 polycyclic aromatic hydrocarbons, 12 polychlorinated biphenyls and 3 nonylphenols were also analyzed [65] DMP, DEP, DIBP, DBP, DMEP, DMPP, DEEP, DNPP, DHXP, BBP DBEP, DCHP, DEHP, DPhP, and DNOP Sea water (25 mL plus 5% w/v NaCl and 10% v/v MeOH) SBSE using a PDMS stir bar, stirring at room temperature for 120 min, and desorption with 200 μL MeOH and 50 μL ACN by sonication for 50 min GC-MS 0.00027–1.63 μg/L - No samples were analyzed The stir bar coated with 150 μl PDMS showed higher extraction efficiency than coated with 50 μL and 75 μL PDMS, and 150 μL PDMS over carbon film. A mix MeOH-ACN showed higher extraction efficiency than MeOH and dichloromethane as desorption solvent [66]

      μ-ECD, micro-electron capture detector; AC, activated carbon; ACN, acetonitrile; BBP, benzylbutyl phthalate; BMA, butyl methacrylate; BMPP, bis(4-methyl-2-pentyl) phthalate; CAR, carboxen; CE, capillary electrophoresis; COFs, covalent organic frameworks; CW, carbowax; DAD, diode-array detector; DAP, diallyl phthalate; DBEP, di(2-butoxyethyl) phthalate; DBP, dibutyl phthalate; DCHP, dicyclohexyl phthalate; DEEP, di(2-ethoxyethyl) phthalate; DEHA, di(2-ethylhexyl) adipate; DEHP, di(2-ethylhexyl) phthalate; DEP, diethyl phthalate; DHXP, dihexyl phthalate; DI, direct immersion; DIBP, diisobutyl phthalate; DIDP, diisodecyl phthalate; DINP, diisononyl phthalate; DIPP, diisopentyl phthalate; DMEP, di(2-methoxyethyl) phthalate; DMP, dimethyl phthalate; DMPP, dimethylethyl phthalate; DNOP, di-n-octyl phthalate; DNPP, di-n-pentyl phthalate; DPhP, diphenyl phthalate; DPP, dipropyl phthalate; DVB, divinylbenzene; EDMA, ethylene dimethacrylate; FID, flame ionization detector; G, graphene; GC, gas chromatography; GO, graphene oxide; HPLC, high-performance liquid chromatography; HS, headspace; IT-SPME, in tube-solid-phase microextraction; LOQ, limit of quantification; MeOH, methanol; MIP, molecularly imprinted polymer; MS/MS, tandem mass spectrometry; MS, mass spectrometry; MWCNTs, multi-walled carbon nanotubes; NPs, nanoparticles; PA, polyacrylate; PAE, phthalic acid ester; PDA, poly(dopamine); PDMS, polydimethylsiloxane; PET, polyethylene terephthalate; PPy, polypyrrole; PS, polystyrene; PVC, polyvinylchloride; SBSE, stir bar sorptive extraction; SPE, solidphase extraction; SPME, solid-phase microextraction; TPB, 2,4,6-triphenoxy-1,3,5-benzene; UHPLC, ultra-performance liquid chromatography; UV, ultraviolet.

      As it has already been said, the fiber coating plays a key role in the SPME of PAEs from water samples. However, the types of commercial fibers are still limited, which reduces their application field. In addition, under certain conditions they have low thermal and chemical stability. Furthermore, they are fragile since they are based on fused silica supports. Consequently, most of the subsequent studies have been focused on developing new highly selective, efficient, inexpensive, and robust SPME fibers with controllable thickness through different coating techniques. For this purpose, a wide variety of new fibers based on the use of carbon-based nanomaterials [40–43], metal oxide nanoparticles (NPs) [39, 44], molecular imprinted polymers (MIPs) [45], covalent organic frameworks (COFs) [46], and bamboo charcoal [47] have been reported, among others.

      Figure 1.3 Schematic representation of the SiO2-PDMS-MWNTs fiber preparation. Reprinted from [43] with permission from The Royal Society of Chemistry. MWNTs, multi-walled carbon nanotubes; TEOS, tetraethoxysilane; TSO-OH, hydroxyl terminated silicone oil.

      Graphene is another of the allotropic forms of carbon that has been used as SPME coating. It consists of a monolayer of sp2 hybridized carbon atoms arranged in a 2D network. Like MWCNTs, graphene has a high surface area, high chemical and thermal stability as well as a high affinity for hydrophobic and aromatic compounds. Then, graphene-polymer nanocomposites have also been used as excellent SPME fiber coatings for the extraction of PAEs. Such is the case of the work developed by Amanzadeh et al. [20] in which a stainless-steel fiber was coated using a new graphene/polyvinylchloride (PVC) material and evaluated successfully as a SPME fiber for the extraction of dipropyl phthalate (DPP), DBP, DEHA, and DEHP from drinking waters and sunflower and olive oil samples. However, even though it was used in the HS mode, a single fiber could be used only 60 times without a significant decrease in the extraction efficiency. As a very interesting experiment, these authors also determined these PAEs in boiling water exposed to a polyethylene terephthalate (PET) bottle. Although the water used did not contain residues of any of the target PAEs at the beginning, residues of DPP and DBP were found at 2.1 and 1.8 μg/L, respectively, after filling this bottle with the same water just after boiling (it was analyzed after cooling). That is, the PAEs with low molecular weight (250.2 g/mol for DPP and 278.3 g/mol for DBP compared to 370.5 g/mol for DEHA and to 390.5 g/mol for DEHP) have larger water solubility, so these kinds of PAEs migrated more easily from PET bottles

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