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Greg McKenna, Horn Professor and the John R. Bradford Chair in the Department of Chemical Engineering in Texas Tech University’s Edward E. Whitacre Jr. College of Engineering, has published his paper, "Testing the Paradigm …
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Abstract: A device test architecture and a reduced device test interface are provided to enable efficient testing of embedded cores and other circuits within devices. The reduced device test interface is achieved using a double data rate (DDR) signaling technique between the tester and the device. The DDR test interface allows the tester to interface to test circuits within the device, such as IEEE 1500 and/or IEEE 1149.1 test circuits, to provide high test data bandwidth to the test circuits using a minimum of test interface signals. The test architecture includes compare circuits that allow for comparison of test response data to be performed within the device. The test architecture further includes a memory for storing the results of the test response comparisons. The test architecture includes a programmable test controller to allow for various test control operations by simply inputting an instruction to the programmable test controller from the external tester. Additional features and embodiments of the device test architecture and reduced test interface are also disclosed.
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We examined the spectral region (2550 to 4000 cm−1) covering the strong OH and NH stretches, with very weak CH stretches observed in the 2800- to 3000-cm−1 range. For the lipid bilayer without channels, we observe in Fig. 3 the typical 3200-cm−1 (yellow) and 3450-cm−1 (green) bands observed for aqueous interfaces in both achiral ppp and ssp polarization combinations. Some controversy exists over the nature of the two features found at the air-water interface, where they merge into one for isotopic dilute HOD in D2O. This suggests that the distinct features are caused by inter- and intramolecular couplings between the OH vibrations (36) or alternatively due to a Fermi-resonance with the OH bend (37). For the water-bilayer interface, the two features could be due to the same couplings or Fermi resonance but are likely due to specific subpopulations of bulk-like water molecules oriented in the field of the charged head groups and water molecules directly interacting with the lipid head groups, respectively. Irrespective of the nature of the two distinct features, the overall distribution of vibrational frequencies reflects the breadth of hydrogen bonding interactions at the water-bilayer interface. In addition to these two bands, we observe in Fig. 3 a band at 3650 cm−1 (blue) that has previously been attributed to weakly hydrogen-bonded water molecules interacting with the ester carbonyl groups of the lipid.
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