Search PubMed⌕ Search

PubMed · 10675981

Optimization of a solid sorbent dynamic personal air sampling method for aldehydes.

Abstract

A solid sorbent personal dynamic air sampling method for aldehydes using chemisorption with 20 percent (w/w) O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine hydrochloride (PFBHA) on Tenax TA has been optimized for several aldehydes. The method for formaldehyde was developed after optimization for valeraldehyde and acrolein. The effects of temperature, intermittent exposure, and flow rate on sampling efficiency were investigated. Vapors of known concentrations were generated in Tedlar gas bags by syringe injection. Aldehyde chemisorption by reaction with 200-mg coated solid sorbent in a Pyrex Tube (7-cm length, 7-mm OD, and 5-mm ID) occurred during dynamic collection with a personal sampling pump operated at 10, 50, or 100 mL/min. The oxime derivatives were 81-87 percent desorbed by shaking with hexane for two minutes or more, resulting in coefficients of variation ranging between 4-7 percent. Aliquots were then injected for gas chromatographic analysis on a nonpolar capillary column with mass spectrometric or 63Ni electron capture detection. Formaldehyde at 8 ppm-hours equivalent to the permissible exposure limit (PEL) concentration was sampled with a recovery of 94 +/- 4 percent at 50.0 +/- 0.5 mL/min. Valeraldehyde and acrolein at their PELs showed no significant differences (P < 0.05) in recoveries at different relative humidities (1 and 90%), temperatures (1, 25, and 40 degrees C), or intermittent sampling protocol. The sampler capacity at 75 percent recovery was at a PFBHA:aldehyde molar ratio of 12:1 at 10.0 +/- 0.1 mL/min, 17:1 at 50.0 +/- 0.5 mL/min, and 26:1 at 100 +/- 1 mL/min.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Y Shen, S S Hee. 2000. Optimization of a solid sorbent dynamic personal air sampling method for aldehydes.. https://doi.org/10.1080/104732200301737

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Three-dimensional porous nano-hydroxyapatite@gelatin composite as efficient adsorbent for uranyl ion removal from low-level radioactive wastewater.

The contamination of water resources by uranyl (UO22+) ions poses significant environmental and health risks, requiring the development of efficient and sustainable remediation strategies. Adsorption-based techniques have emerged as promising approaches in the field of UO22+ removal, but the design of cost-effective, high-capacity, and environmentally friendly adsorbents remains challenging. In this study, a three-dimensional porous nano-hydroxyapatite@gelatin (nHAP@Ge) composite was synthesized through glutaraldehyde cross-linking, combining the structural stability of Ge with the high uranium affinity of nHAP. The optimized nHAP@Ge, with a nHAP:Ge mass ratio of 1:0.5, exhibited exceptional UO22+ removal efficiency (97 %), along with high adsorption capacity (364.03 mg/g). Systematic characterizations using scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Fourier transform infrared (FT-IR) spectroscopy, and X-ray photoelectron spectroscopy (XPS) methods revealed that the porous structure and surface functional groups (-OH, Ca2+, and PO43-) of the material synergistically contributed to binding UO22+ species. Furthermore, the incorporation of nHAP into the Ge framework resulted in enhanced thermal stability while significantly improving the UO22+ adsorption performance. This work presents a scalable, eco-friendly, and recyclable strategy for the effective treatment of uranium-contaminated water, with potential applications in nuclear wastewater treatment and environmental remediation.

Adsorption↗

Dual radiolabeling to study protein adsorption competition in relation with hemocompatibility.

Human fibrinogen (Fg) and albumin (HSA) were labeled with (3)H and (14)C, respectively. Dual counting allowed the adsorbed amount of the two proteins to be determined simultaneously. Single adsorption, adsorption of the two proteins in competition, but also exchange (substitution by molecules of the same nature) and displacement (desorption under the action of the other protein) experiments were performed on two model surfaces, glass and polystyrene (PS), as well as on pure polyvinylchloride (PVC-s) and on PVC from blood bag (PVC-b). As expected, the adsorbed amount of a single protein is higher on a hydrophobic compared to a hydrophilic surface. When the two proteins are adsorbed in competition, they are found in equal proportion on glass, while HSA is twice more abundant than Fg on PS and PVC-s and about six times more abundant on PVC-b. This trend is related to an increase of the water contact angle of the substrates. For PVC-b, the contact angle is affected by the presence of aliphatic components exposed at the extreme surface, as determined by angle-resolved X-ray photoelectron spectroscopy. In exchange and displacement experiments, the first adsorbed molecules remain dominating on PS while they can be removed from glass. Given the known importance of HSA and Fg adsorption for the fate of materials placed in contact with blood, the method described in this paper may be used as a first approach to orient the design of surfaces with improved hemocompatibility.

Adsorption↗

Effective immobilization of subunit protein in mesoporous silica modified with ethanol.

Ethoxylated FSM-type mesoporous silica (folded-sheet mesoporous material) with a pore diameter of 6.2 nm (FSM6.2) remarkably enhances rigidly of the structure in aqueous solutions. The esterified material could be used successfully as an adsorbent to accommodate subunit protein, methemoglobin (Fe(3+)). Furthermore, methemoglobin (Fe(3+)) in the pores of ethoxy-FSM is maintained a peroxidase activity similar to the native, indicating methemoglobin retains its fore subunit structure in the pores of FSM6.2.

Adsorption↗