Thermal desorption is used extensively in exhaled breath volatile organic compound (VOC) analysis, and it is often necessary to store the adsorbent tube samples before analysis. The possible introduction of storage artefacts is an important potential confounding factor in the development of standard methodologies for breath sampling and analysis. The stability of VOCs trapped from breath samples onto a dual bed Tenax® TA:Carbograph adsorbent tube and stored  −80°C was studied over 12.5 month. 25 samples were collected from a single male participant over 3 h and then stored at  −80 °C. Randomly selected adsorbent tubes were subsequent analysed by thermal desorption-gas chromatography-mass spectrometry at 5 times points throughout the 12.5 month of the study. Toluene-d8, decane-d22 and hexadecane-d34 internal standards were used to manage the instrument variability throughout the duration of the study. A breath-matrix consisting of 161 endogenous and 423 exogenous VOC was created. Iterative orthogonal partial least squared discriminant analysis (OPLS-DA) and principal components analysis (PCA) indicated that it was not possible to detect storage artefacts at 1.5 month storage. By 6 month storage artefacts were discernible with significant changes observed for 27% of the recovered VOC. Endogenous VOC were observed to be more susceptible to storage. A paired two-tailed t-test on the endogenous compounds indicated that the maximum storage duration under these conditions was 1.5 month with 94% of the VOCs stable. This study indicates that a prudent approach is best adopted for the storage of adsorbent samples; storage times should be minimised, and storage time examined as a possible discriminatory factor in multivariate analysis.

Exhaled volatile organic compounds (VOCs) are of interest due to their minimally invasive sampling procedure. Previous studies have investigated the impact of exercise, with evidence suggesting that breath VOCs reflect exercise-induced metabolic activity. However, these studies have yet to investigate the impact of maximal exercise to exhaustion on breath VOCs, which was the main aim of this study. Two-litre breath samples were collected onto thermal desorption tubes using a portable breath collection unit. Samples were collected pre-exercise, and at 10 and 60 min following a maximal exercise test (VO2MAX). Breath VOCs were analysed by thermal desorption-gas chromatography-mass spectrometry using a non-targeted approach. Data showed a tendency for reduced isoprene in samples at 10 min post-exercise, with a return to baseline by 60 min. However, inter-individual variation meant differences between baseline and 10 min could not be confirmed, although the 10 and 60 min timepoints were different (p = 0.041). In addition, baseline samples showed a tendency for both acetone and isoprene to be reduced in those with higher absolute VO2MAX scores (mL(O2)/min), although with restricted statistical power. Baseline samples could not differentiate between relative VO2MAX scores (mL(O2)/kg/min). In conclusion, these data support that isoprene levels are dynamic in response to exercise.

Chlorine‐based disinfectants protect pool water from pathogen contamination but produce potentially harmful halogenated disinfection by‐products (DBPs). This study characterized the bioaccumulation and elimination of exhaled DBPs post‐swimming and investigated changes in exhaled breath profiles associated with chlorinated pool exposure. Nineteen participants provided alveolar‐enriched breath samples prior to and 5, 90, 300, 510, and 600 minutes post‐swimming. Known DBPs associated with chlorinated water were quantitated by thermal desorption‐gas chromatography‐mass spectrometry. Two distinct exhaled DBP elimination profiles were observed. Most participants (84%) reported peak concentrations immediately post‐swimming that reduced exponentially. A sub‐group exhibited a previously unobserved and delayed washout profile with peak levels at 90 minutes post‐exposure. Metabolomic investigations tentatively identified two candidate biomarkers associated with swimming pool exposure, demonstrating an upregulation in the hours after exposure. These data demonstrated a hitherto undescribed exhaled DBP elimination profile in a small number of participants which contrasts previous findings of uniform accumulation and exponential elimination. This sub‐group which exhibited delayed peak‐exhaled concentrations suggests the uptake, processing, and immediate elimination of DBPs are not ubiquitous across individuals as previously understood. Additionally, non‐targeted metabolomics highlighted extended buildup of compounds tentatively associated with swimming in a chlorinated pool environment that may indicate airway responses to DBP exposure.

With high-grade apatite resources exhausted and economic development, enhancing the apatite quality from calcium gangue such as dolomite has a great significance for production. However, it is difficult to separate apatite from dolomite effectively due to the similar surface properties. In this study, the N-carboxybutyl chitosan (CBC) was tested as a potential selective depressant to separate apatite from dolomite in the sodium oleate (NaOL). Flotation results of single mineral and artificially mixed mineral confirmed the selective depression effect of CBC. The depression mechanism of CBC was investigated using wettability analysis, Fourier Transform Infrared (FTIR), and X-ray Photoelectron Spectroscopy (XPS) analyses. The results indicated that the CBC adsorption quantity and intensity on the dolomite surface more than that on the apatite surface, which was due to CBC absorbed on apatite surface by hydrogen bonding, while absorbed on dolomite surface mainly through chemical chelating between Ca on the mineral surface and -COOon the depressant. These adsorption differences led to the flotation separation of the two minerals.