Highly integrated direct conversion receiver for GSM/GPRS/EDGE with on-chip 84-dB dynamic range continuous-time /spl Sigma//spl Delta/ ADC

This paper describes a highly digitized direct conversion receiver of a single-chip quadruple-band RF transceiver that meets GSM/GPRS and EDGE requirements. The chip uses an advanced 0.25-/spl mu/m BiCMOS technology. The I and Q on-chip fifth-order single-bit continuous-time sigma-delta (/spl Sigma//spl Delta/) ADC has 84-dB dynamic range over a total bandwidth of /spl plusmn/135 kHz for an active area of 0.4 mm/sup 2/. Hence, most of the channel filtering is realized in a CMOS IC where digital processing is achieved at a lower cost. The systematic analysis of dc offset at each stage of the design enables to perform the dc offset cancellation loop in the digital domain as well. The receiver operates at 2.7 V with a current consumption of 75 mA. A first-order substrate coupling analysis enables to optimize the floor plan strategy. As a result, the receiver has an area of 1.8 mm/sup 2/.     

Microstructural Investigation of Protective and Non-Protective Oxides on 11% Chromium Steel

FIB, SEM and STEM/EDX were used to investigate X20 stainless-steel samples exposed to dry O₂, or O₂ containing 40% H₂O, with a flow velocity of 0.5 cm/s or 5 cm/s, for 168 hr or 336 hr at 600°C. Thin protective Cr-rich (Cr,Fe)₂O₃ was maintained on the samples exposed to dry O₂, even after 336 hr, and on the sample exposed to O₂/H₂O mixture with the low-flow velocity (0.5 cm/s) for 168 hr. The oxide scale formed in the latter environment contained less Cr, due to Cr loss through CrO₂(OH)₂ evaporation. Breakaway oxidation occurred on the samples exposed in high-gas-flow velocity for shorter time (168 hr) or in low-gas-flow velocity (0.5 cm/s) for longer time (336 hr). The breakaway scales featured a two-layered structure: an outward-growing oxide “island” consisting of almost pure hematite (α-Fe₂O₃), and an inward-growing oxide “crater” consisting of (Cr,Fe)₃O₄. The transition from a thin protective (Cr,Fe)₂O₃ scale to a non-protective thick scale on this martensitic/ferritic steel originated locally and was followed by rapid oxide growth, resulting in a thick scale that covered the whole sample surface.     

State-variable planning under structural restrictions: algorithms and complexity

Computationally tractable planning problems reported in the literature so far have almost exclusively been defined by syntactical restrictions. To better exploit the inherent structure in problems, it is probably necessary to study also structural restrictions on the underlying state-transition graph. The exponential size of this graph, though, makes such restrictions costly to test. Hence, we propose an intermediate approach, using a state-variable model for planning and defining restrictions on the separate state-transition graphs for each state variable. We identify such restrictions which can tractably be tested and we present a planning algorithm which is correct and runs in polynomial time under these restrictions. The algorithm has been implemented and it outperforms Graphplan on a number of test instances. In addition, we present an exhaustive map of the complexity results for planning under all combinations of four previously studied syntactical restrictions and our five new structural restrictions. This complexity map considers both the optimal and non-optimal plan generation problem.     

Aspects of reconfigurable and flexible fixtures

The design and manufacture of fixtures and other dedicated tooling for positioning of workpieces are among the major cost drivers in product industrialization. This has spurred research and commercial interest towards other fixturing solutions like reconfigurable fixtures, with the ability to be changed, or “reconfigured”, to suit different parts and products. When reconfiguring, the product interface not only has to be moved but moved to a desired position and orientation. Several different approaches have been used to move and position these devices, all with their own advantages and disadvantages. This article presents different methods used to position and reconfigure flexible fixture devices using a parallel kinematic device as a case. Discussing the different ways to reconfigure a flexible device, the article aims to arrange the techniques according to their key features.     

Low-voltage 32 Msample/s parallel pipelined switched-current ADC

A parallel switched-current A/D converter is presented. Eight time-interleaved switched-current ADCs operating at 4 Msample/s are used to increase the sampling rate. With channel compensation, the measured SFDR is >50 dB at 32 Msample/s with f_m=1.13 MHz. The performance of this experimental design is limited by noise and a fixed-pattern timing error that is not removed by the compensation algorithm     

Thermodiffusion‐Assisted Pyroelectrics—Enabling Rapid and Stable Heat and Radiation Sensing

Sensors for monitoring temperature, heat flux, and thermal radiation are essential for applications such as electronic skin. While pyroelectric and thermoelectric effects are suitable candidates as functional elements in such devices, both concepts show individual drawbacks in terms of zero equilibrium signals for pyroelectric materials and small or slow response of thermoelectric materials. Here, these drawbacks are overcome by introducing the concept of thermodiffusion‐assisted pyroelectrics, which combines and enhances the performance of pyroelectric and ionic thermoelectric materials. The presented integrated concept provides both rapid initial response upon heating and stable synergistically enhanced signals upon prolonged exposure to heat stimuli. Likewise, incorporation of plasmonic metasurfaces enables the concept to provide both rapid and stable signals for radiation‐induced heating. The performance of the concept and its working mechanism can be explained by ion–electron interactions at the interface between the pyroelectric and ionic thermoelectric materials.     

Synthesis,characterization, and study of thermal properties of methyl-substituted arylene sulfone ether polyimides,polyamides, and poly(amide–imides)

A number of methyl-substituted bis[(phenyleneoxy) sulfone] dianilines were synthesized and reacted with pyromellitic dianhydride (PMDA), benzophenone tetracarboxylic acid dianhydride (BTDA), terephthaloyl chloride (TPC), isophthaloyl chloride (IPC), and trimellitic anhydride acid chloride (TMAC) to prepare a series of polyimides, polyamides, and poly(amide–imides), respectively. Low temperature solution and interfacial polymerization techniques were utilized to prepare the above polymers. Most of the polymers prepared formed tough, transparent flexible films. The prepared polymers were characterized by solution viscosity, thermal gravimetric analysis (dynamic and isothermal), and differential scanning calorimetry. The effect of the number and the ring substitution of methyl groups on polymer properties is discussed.     

Impact of humidity on the ozone initiated oxidation of limonene, delta3-carene, and alpha-pinene

The effect of water on the initial secondary organic aerosol (SOA) formation from gas-phase ozonolysis of limonene, delta3-carene, and alpha-pinene (-3 and approximately 1.5 x 10(11) molecule cm(-3) reacted) has been investigated in a flow reactor at controlled relative humidity (RH), temperature (298 +/- 0.4 K), and reaction time (270 +/- 2 s). Low amounts of terpene converted minimize the impact of secondary reactions. A comparison of the SOA formation from the three terpenes was made for initial rate of reactions being around 7.5 x 10(8) and 15 x 10(8) molecule cm(-3) s(-1). The most efficient species in producing SOA was limonene, while alpha-pinene was the least efficient. The results showed that an enhancement in water vapor concentration (<2-85% RH) caused an increase in both integrated mass (M10-300nm) and total number (N10-300nm). The effect on number and mass were a factor of 2-3 and 4-8, respectively. Physical water up-take can partly explain the increase in mass, but not the observed increase in number. Therefore it was concluded that the increase in water concentration must, by a gas-phase reaction, produce more low volatility product(s).     

Adsorption and surface complexation study of L-DOPA on Rutile (α-TiO₂) in NaCl solutions

Dihydroxyphenylalanine (DOPA) and similar molecules are of considerable interest in studies of bioadhesion to minerals, solar cells involving titanium dioxide, and biomedical imaging. However, the extent and mechanisms of DOPA adsorption on oxides in salt solutions are unknown. We report measurements of DOPA adsorption on well-characterized rutile (α-TiO?) particles over a range of pH, ionic strength, and surface coverage as well as a surface complexation model analysis establishing the stoichiometry, model surface speciation, and thermodynamic equilibrium constants, which permits predictions in more complex systems. DOPA forms two surface species on rutile, the proportions of which vary strongly with pH but weakly with ionic strength and surface loading. At pH < 4.5 a species involving four attachment points ("lying down") is important, whereas at pH > 4.5 a species involving only two attachment points via the phenolic oxygens ("standing up") predominates. Based on evidence of strong attachment of DOPA to titanium dioxide from single molecule AFM (Lee, H. et al., Proc. Natl. Acad. Sci.2006, 103, 12999-12003) and studies of catechol adsorption, one or more of the DOPA attachments for each species is inner-sphere, the others are likely to be H-bonds.     

Influence of OH scavenger on the water effect on secondary organic aerosol formation from ozonolysis of limonene, Delta3-carene, and alpha-pinene

The effect of OH scavengers on how water vapor influences the formation of secondary organic aerosol (SOA) in ozonolysis of limonene, Delta3-carene, and alpha-pinene at low concentrations has been investigated by using a laminar flow reactor. Cyclohexane and 2-butanol (3-40 x 10(13) molecules cm(-3)) were used as scavengers and compared to experiments without any scavenger. The reactions were conducted at 298 K and at relative humidities between <10 and 80%. The yield of SOA decreased in the order "no scavenger" > 2-butanol > cyclohexane. The effect of water vapor was similar for 2-butanol and without a scavenger, with an increase in particle number and mass concentration with increasing relative humidity. The water effect for cyclohexane was more complex, depending on the terpene, scavenger concentration, and SOA concentration. The water effect seems to be influenced by the HO2/RO2 ratio. The results are discussed in relation to the currently suggested mechanism for alkene ozonolysis and to atmospheric importance. The results imply that the ozone-initiated oxidation of terpenes needs revision in order to fully account for the role of water in the chemical mechanism.