Structural Test Approach for Embedded Analog Circuits Based on a Built-in Current Sensor

This paper presents a test method based on the analysis of the dynamic power supply current, both quiescent and transient, of the circuit under test. In an off-chip measurement, the global interconnect impedance associated with the chip package and the test equipment and, also, the chip input/output cells will complicate the extraction of the information provided by the current waveform of the circuit under test. Thus, the supply current is measured on-chip by a built-in current sensor integrated in the die itself. To avoid the effective reduction of the voltage supply, the measurement is performed in parallel by replicating the current that flows through selected branches of the analog circuit. With the aim of reducing the test equipment requirements, the built-in current sensor output generates digital level pulses whose width is related to the amplitude and duration of the circuit current transients. In this way the defective circuit is exposed by comparing the digital signature of the circuit under test with the expected one for the fault-free circuit. A fault evaluation has been carried out to check the efficiency of the proposed test method. It uses a fault model that considers catastrophic and parametric faults at transistor level. Two benchmark circuits have been fabricated to experimentally verify the defect detection by the built-in current sensor. One is an operational amplifier; the other is a structure of switched current cells that belongs to an analog-to-digital converter.     

Structure and properties of lead and lead sulfide nanoparticles in natural zeolite

We have synthesized lead and lead sulfide nanoparticles embedded in a natural zeolite (clinoptilolite) matrix by a simple hydrothermal process. The process steps involve the partial removing of the natural cations in clinoptilolite, the ion-exchange process to enclose Pb ions and nanoparticles and finally a sulfuration process at different temperatures to obtain lead sulfide phases in the zeolite matrix. The samples were studied by X-ray diffraction, diffuse reflectance spectroscopy, energy dispersive X-ray spectroscopy, X-ray photon spectroscopy and transmission electron microscopy. The experimental results show the inclusion of three Pb species with different valence states after the Pb ion-exchange step, namely Pb²⁺, Pb⁴⁺, and Pb⁰. At the end of the process, two simultaneous lead sulfide crystalline phases, PbS (Galena) and PbS₂ (tetragonal) were synthesized in the clinoptilolite matrix. The optical absorption spectra of the samples show the exciton absorption peaks typical of colloidal PbS nanoparticles. The average size of the PbS nanoparticles was about 10 nm and their crystalline structure was determined from diffraction electron patterns. The high-pressure phase PbS₂ was also identified and its formation was attributed to the influence of the special conditions of clinoptilolite matrix as crystallization media to induce some selective nucleation process of this crystalline phase.     

The magnetics diagnostic set for ITER

The current status of the ITER magnetics diagnostic is summarised. The various risks are discussed on the basis of when they could be present during ITER operation and appropriate mitigation is reviewed. An implementation risk or common mode operation failure risk to the magnetic diagnostic can only be mitigated by diversity. All identified risks are being handled with ongoing research and development to minimise these risks. A reasonable level of design and manufacturing diversity has been therefore introduced in the procurement and installation plans, in order to optimise overall reliability avoiding dispersion of resources.     

Synthesis and characterization of aniline copolymers containing carboxylic groups and their application as sensitizer and hole conductor in solar cells

Copolymers of m-aminobenzoic acid and o-anisidine doped with p-toluenesulphonic acid in different proportions were successfully synthesized by oxidative polymerization. The copolymers were characterized by FT-IR, UV–vis, ¹H NMR and EPR spectroscopies, cyclic voltammetry, conductivity and SEM. The copolymer with equivalent amounts of the monomers o-anisidine and m-aminobenzoic acid presented the highest conductivity, The EPR analyses and SEM images show that this copolymer provides more homogeneous films with particle size distribution of approximately 1–2 μm. The copolymer with a high fraction of o-anisidine gives rises to films with larger particle sizes and a more defined electrochemical process. The m-aminobenzoic acid monomer was intentionally chosen in order to promote a better electronic coupling between the conducting copolymer and the TiO₂ surface. The copolymers were tested as both sensitizers and hole conducting materials in dye-sensitized solar cells. The device assembled using the copolymer with the highest proportion of m-aminobenzoic acid units as sensitizer produced the highest photocurrent (I_sc = 0.254 mA cm^?2) and photovoltage (V_oc = 0.252 V) at 100 mW cm^?2. The energy diagram shows that although the electronic injection from the conducting polymer excited state is an allowed process the regeneration of the positive charges created after the electron transfer process is forbidden, thus explaining the low efficiency of solar energy conversion. When this copolymer was applied as a hole conducting material, an improvement in the V_oc to 0.4 V, was observed, indicating that this material is more suitable for charge transport when applied in this type of solar cells.     

Synthesis of porous hydroxyapatites by combination of gelcasting and foams burn out methods

The biocompatibility and the osteoconductive behavior of hydroxyapatite (OHAp) ceramics are well established. Bioceramics made of OHAp are available in dense and porous form. Recently it has been proved that the volume of bone ingrowth at early times is primarily interconnectivity dependent. A new method for the obtention of porous OHAp ceramics that combine the in situ polymerization (gel casting method) and the foams burn out is proposed. Four polyurethane foams with different cells/cm were used. The foams were fully filled of an OHAp polymerizable suspension that after gelled produced very homogeneous and strong green bodies. After different thermal treatments the green bodies yield porous OHAp ceramics that were a replica of the foams used. Materials used in this work were studied by X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy (SEM), N₂ adsorption isotherm, particle size distribution, and Hg porosimetry. Porous pieces of OHAp obtained are constituted by polyhedral-like particles (0.45–1.0 m) that are surrounded by an interconnected network of pores. A bimodal distribution of the pores size between 30.8–58.6 and 1.0–1.2 m has been observed. The size of the interconnected pores (30.8–58.6 m) was controled as a function of the cells/cm of the foam while the volume of the small pores was modified as a function of the sintering time. The presence of pores could promote the bone ingrowth and also could be used to insert different drugs, which makes these porous pieces a potential candidate to be used as non-load-bearing bone implants and as drug delivery systems.     

Refining Copper Scrap by Gas Injection

Using a porous plug or a tuyere, a copper bath composed of electrical scrap may be oxidized or deoxidized through the application of gas injection. Dry air and a hydrocarbon were used in the tests at scales of 16 kg, 400 kg and 16 t.     

Analysing metals in bottle‐grade poly(ethylene terephthalate) by X‐ray fluorescence spectrometry

After a rigorous cleaning process, recycled food‐grade poly(ethylene terephthalate) (PET), can be mixed with virgin PET resin in different concentrations and used for packaging of soft drinks. Therefore, it is important to have an experimental method to distinguish the presence of recycled polymer in a batch and to check its “true quality.” One of the issues to be verified is the presence of inorganic contaminants due to the recycling process. X‐ray fluorescence technique is one alternative for this kind of analysis. The results obtained in this work show that bottle‐grade PET samples (PET‐btg) are made either via direct esterification or by a transesterification process. Samples that were subjected to thermo‐mechanical processings (superclean® processing, PET‐btg blends processed in our laboratory and soft drink PET packaging) present Fe Kα emission lines with higher intensities than those presented by virgin bottle‐grade PET. After applying principal component analysis, it can be concluded that Fe is an intrinsic contaminant after the recycling process, furnishing a way to indicate class separations of PET‐btg. A calibration and validation partial least squares model was constructed to predict the weight percent of post‐consumption bottle‐grade PET in commercial PET samples. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Nanoparticles of 4,7-dichloro-2-quinolinemethylacrylate-based copolymers and their potential cytotoxic activity on human breast carcinoma cells

In this article, an improved synthesis strategy of the potent anticancer compound 4,7-dichloro-2-quinolinemethanol (QM) and its acrylate ester 4,7-dichloro-2-quinolinemethylacrylate (AQM) are described. AQM is copolymerized using free-radical polymerization with N-vinyl-2-pyrrolidone (VP) and the copolymers obtained from different molar ratios of monomers are subjected to nanoprecipitation to produce suspensions of nanoparticles (NPs) in phosphate buffered saline (PBS). The smallest and stable NPs are prepared with the AQM-VP copolymers 45:55 and 40:60 (118.9 and 128.7 nm in diameter, respectively) at 1 mg mL⁻¹, and along with AQM and QM, are evaluated for their cytotoxic activity on MDA-MB-453 breast carcinoma cells using MTT bioassay. AQM and QM are highly cytotoxic (IC₅₀: 19 and 41 μM, respectively); however, the NPs are not cytotoxic in the range of the assayed concentrations. These results contribute to the search for new polymeric NPs with potential application as QM delivery systems for the treatment of cancer or other diseases treatable with QM. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47545.