A sulfonate level of 1.32 mol% was achieved.
On the contrary, the highest production of di- and trioleoyl xylitol, corresponding to 94 mol%, was achieved in n-hexane.
The detection limitation of 7.2×10 15 mol L−1 was achieved, which can be attributed to the synergistic effect of combining BDD with Au-NPs, aptamers, and MCH.
Finally, the colorimetric experiment result was observed and conveniently monitored by the naked eye, and a visual detection limit of 4 × 10−6 mol L−1 was achieved.
The optimal photo-degradation rate of 3.47 × 10−2 mol dm−3 min−1 was achieved at 60 ppm CR, pH 3, aeration rate of 5 dm3 min−1 and TiO2 N loading of 4 g dm−3.
In this work, a detection limit of 5 × 10−12 mol L−1 was achieved for the detection of complementary DNA sequence [65].
High selectivity for PFAFs with only two RF groups, up to ca. 75 mol %, was achieved at the expense of C60 conversion by limiting the reaction time (an approach similar to that used for the synthesis of La@C82 n-C8F17 2 and for the selective preparation of C60(C60)2).
At these optimum conditions, 60.8 mol hydrogen production was achieved which was 8% higher than that observed from the screening experiment.
The highest H2 productivity (0.276 mol H2/h kgcat) was achieved with 1 g/L of 1 wt% Au/TiO2 P25 catalyst by using a 113 W/m2 UVA irradiation.
Few fluorinated intermediates were detected either in solution or in gas phase by ESI-MS and ATD-GC/MS, and high yield of fluoride (16.7 mol F−/mol PFOS) was achieved, which indicates that PFOS can be completely defluorinated by this method.
The results showed that the acclimated excess sludge was able to produce PHBHHx, and the maximum output (505.6 mg/L PHBHHx containing 6.34 mol% HHx) was achieved with conditions of the continuous aeration, nitrogen and phosphorus limitation, and adequate carbon source implemented by pulse feeding 0.5 g/L sodium laurate every 4 h.
