Insertion loss and misalignment tolerance in multimode tapered waveguide bends

Experimental measurements of laterally tapered multimode waveguide bends fabricated photolithographically on FR4 printed circuit board establish that the product of the mean insertion loss (in linear units) and the mean source misalignment tolerance is a constant which depends only on the taper ratio TR (input width/output width) and not on the radius of curvature R. The minimum loss of 0.78 dB occurs in the special case of TR = 0.8, R = 14 mm. Together, these form waveguide layout design rules for board-to-board and chip-to-chip optical interconnects

Acetone in the Atmosphere of Hong Kong, Abundance, Sources and Photochemical Precursors

Intensive field measurements were carried out at a mountain site and an urban site at the foot of the mountain from September to November 2010 in Hong Kong. Acetone was monitored using both canister air samples and 2,4-dinitrophenylhydrazine cartridges. The spatiotemporal patterns of acetone showed no difference between the two sites (p > 0.05), and the mean acetone mixing ratios on O3 episode days were higher than those on non-O3 episode days at both sites (p < 0.05). The source contributions to ambient acetone at both sites were estimated using a receptor model i.e. Positive Matrix Factorization (PMF). The PMF results showed that vehicular emission and secondary formation made the most important contribution to ambient acetone, followed by the solvent use at both sites. However, the contribution of biogenic emission at the mountain site was significantly higher than that at the urban site, whereas biomass burning made more remarkable contribution at the urban site than that at the mountain site. The mechanism of oxidation formation of acetone was investigated using a photochemical box model. The results indicated that i-butene was the main precursor of secondary acetone at the mountain site, while the oxidation of i-butane was the major source of secondary acetone at the urban site.Department of Civil and Environmental Engineerin

Seasonal variation of tropospheric methyl bromide concentrations: Constraints on anthropogenic input

Although removal of tropospheric methyl bromide (CH3Br) is dominated by the reaction with the seasonally varying hydroxyl (HO) radical concentration, the anticipated corresponding seasonal dependence of CH3Br, as found for other gases with major HO sinks, has been sought previously without success [WMO, 1995]. Our observations of northern hemispheric boundary layer CH3Br concentrations do reveal substantial seasonal changes. The high latitude CH3Br North/South interhemispheric concentration ratio (IHR) varies from a maximum of 1.35±0.04 (1σ) in March-April to 1.10±0.04 in September, with an equal area and seasonally (EAS) weighted average IHR of 1.21±0.03. These observations suggest northern hemispheric emissions are about 15 kilotons/year less than when an IHR of 1.3 is considered [WMO, 1995]. The observed seasonality also partially explains the differences in the IHR reported by several research groups [WMO, 1995] and places needed constraints on the magnitude and seasonality of sources and sinks of CH3Br