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An effective method utilising pressurised fluid extraction (PFE) to simultaneously extract polycyclic aromatic hydrocarbons (PAHs) and their polar oxidation products from atmospheric particulate matter (PM) is presented. The PFE method is advantageous over the traditional Soxhlet extraction due to its lower solvent consumption (9 mL compared to 90 mL) and shorter extraction time (15 min versus 18 h). Seventy compounds including PAHs and polar PAH oxidation products containing carbonyl (oxy-PAHs), hydroxyl (hydroxy-PAHs), and carboxylic acid (carboxy-PAHs) groups were targeted in the extraction of two different PM matrices: wood smoke (WS) and diesel exhaust (DE) PM. The PFE method was optimised and then compared to Soxhlet extraction for both PM matrices. The overall amounts of PAHs and their derivatives extracted from WS PM were slightly higher for the optimised PFE method (1849 ± 21 and 1863 ± 25 µg g?1 with dichloromethane (DCM) and methanol (MeOH), respectively) than those obtained with Soxhlet extraction (1726 ± 33 and 1769 ± 22 µg g?1 with DCM and MeOH, respectively). For DE PM (standard reference material (SRM) 2975) the overall amounts extracted by both methods were similar (average of 165 ± 6 µg g?1), agreeing with previously published values. The detailed evaluation of extraction efficiencies for WS PM showed similar amounts for unfunctionalised PAHs (1100 µg g?1) for both methods and solvents. For DE PM the mass yields for PAHs using PFE with DCM (62 ± 1 µg g?1) were the highest and nearly 20% higher than those obtained with MeOH (53 ± 2 µg g?1). The total mass yields of carboxy and hydroxy-PAHs from WS PM were also similar (412 ± 18 and 407 ± 11 µg g?1) for PFE and Soxhlet with MeOH, and higher than when DCM was used (371 ± 5 and 379 ± 12 µg g?1 for PFE and Soxhlet, respectively). For both matrices, the PFE yields for oxy-PAHs were higher than those obtained with Soxhlet.  相似文献   
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An alkylated semiconducting polymer comprising alternating bithiophene‐[all]‐S,S‐dioxide and aromatic monothiophene units in the polymer backbone was synthesized with the intent of modifying the energy gap and lowest unoccupied molecular orbital for use as a stable n‐type semiconductor. Films spun from this semiconducting polymer were characterized utilizing X‐ray scattering, near edge X‐ray absorption fine structure spectroscopy, ultraviolet photoelectron spectroscopy, and thin‐film field effect transistors to determine how oxidation of the thiophene ring systems impacts the structural and electronic properties of the polymer. The thiophene‐S,S‐dioxide polymers have lower optical and electrical band gaps than corresponding thiophene polymers. X‐ray scattering results indicate that the polymers are well ordered with the π–π stacking distances increased by 0.4 Å relative to analogous thiophene polymers. The electrical stability of these polymers is poor in transistors with a drop in the field effect mobility by approximately one order of magnitude upon addition of just 5% of the thiophene‐S,S‐dioxide unit in a copolymer with thiophene. © 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2013  相似文献   
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A geometric perspective involving Grammian and frame operators is used to derive the entire family of Welch bounds. This perspective unifies a number of observations that have been made regarding tightness of the bounds and their connections to symmetric k-tensors, tight frames, homogeneous polynomials, and t-designs. In particular, a connection has been drawn between sampling of homogeneous polynomials and frames of symmetric k-tensors. It is also shown that tightness of the bounds requires tight frames. The lack of tight frames of symmetric k-tensors in many cases, however, leads to consideration of sets that come as close as possible to attaining the bounds. The geometric derivation is then extended in the setting of generalized or continuous frames. The Welch bounds for finite sets and countably infinite sets become special cases of this general setting.  相似文献   
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