Optimal Selective Count Compatible Runlength Encoding for SOC Test Data Compression

Test data volume amount is increased multi-fold due to the need of quality assurance of various parts of the circuit design at deep submicron level. Huge memory is required to store this enormous test data which not only increases the cost of the ATE but also the test application time. This paper presents an optimal selective count compatible run length (OSCCPRL) encoding scheme for achieving maximum compression for reduction of the test cost. OSCCPRL is a hybrid technique that amalgamates the benefits of other two techniques: 10 Coded run length (10 C) and Selective CCPRL (SCCPRL) proposed here. These techniques work on improvement of the 9 C and CCPRL techniques. In OSCCPRL, entire data is segmented in blocks and further compressed using inter block and intra block level merging techniques. SCCPRL technique is used for encoding the compatible blocks while the 10C is used to do encoding at sub block (half block length) level. In case, if no compatibility is found at block/sub block level then the unique pattern is held as such in the encoded data along with the necessary categorization bits. The decompression architecture is described and it is shown how by just the addition of few states of FSM, better test data compression can be achieved as compared to previous schemes. The simulation results performed for various ISCAS benchmarks circuits prove that the proposed OSCCPRL technique provides an average compression efficiency of around 80 %.     

Surface treatment of hematite photoanodes with zinc acetate for water oxidation

A simple and inexpensive method to form a hematite photoanode for efficient water oxidation is reported. A very thin ZnO overlayer was deposited on top of a thin film of hematite and found, compared with non-treated hematite, to increase the photocurrent and reduce the onset potential for generating oxygen from water. After 3 cycles of ZnAc treatment, the photocurrent increased more than 40% to 1.08 mA cm(-2) at 0.23 V vs. Ag/AgCl and onset potential for water oxidation shifted by -170 mV. It is proposed that the ZnO overlayer changes the flat band potential of hematite and reduces the surface defects.     

Effect of the Nanodiamond Host on a Nitrogen‐Vacancy Color‐Centre Emission State

Control over the quantum states of individual luminescent nitrogen‐vacancy (NV) centres in nanodiamonds (NDs) is demonstrated by careful design of the crystal host: its size, surface functional groups, and interfacing substrate. By progressive etching of the ND host, the NV centres are induced to switch from latent, through continuous, to intermittent or “blinking” emission states. The blinking mechanism of the NV centre in NDs is elucidated and a qualitative model proposed to explain this phenomenon in terms of the centre electron(s) tunnelling to acceptor site(s). These measurements suggest that the substrate material and its proximity to the NV are responsible for the fluorescence intermittency.     

Removal of natural hormone estrone from secondary effluents using nanofiltration and reverse osmosis

The rejection of steroid hormone estrone by nanofiltration (NF) and reverse osmosis (RO) membranes in treated sewage effluent was investigated. Four NF/RO membranes with different materials and interfacial characteristics were utilized. To better understand hormone removal mechanisms in treated effluent, effluent organic matters (EfOM) were fractionated using column chromatographic method with resins XAD-8, AG MP-50 and IRA-96. The results indicate that the presence of EfOM in feed solution could enhance estrone rejection significantly. Hydrophobic acid (HpoA) organic fraction made a crucial contribution to this “enhancement effect”. Hydrophobic base (HpoB) could also improve estrone rejection while hydrophobic neutral (HpoN) and hydrophilic acid (HpiA) with low aromaticity had little effects. The increment in estrone rejection was predominantly attributed to the binding of estrone by EfOM in feed solutions, which led to an increase in molecular weight and appearance of negative charge (for the HpoA case) and thus an increased level of estrone rejection. However, the improvement of estrone rejection by HpoA decreased with increasing calcium ion concentration. The important conclusion of this study is, first, hydrophobic acid macromolecules are recommended to be added into feed water to improve the rejection of trace hormone during NF/RO membrane process, and, second, removal of calcium ions via pretreatment and application of membrane with more negative charge at its interface can greatly intensify this “enhancement effect”.     

High Temperature Corrosion Behavior of Cold Spray Ni-20Cr Coating on Boiler Steel in Molten Salt Environment at 900 °C

Cold spray is an emerging technology that produces high density metallic coatings with low oxide contents and high thermal conductivity, which makes them ideal for high temperature corrosion resistance. In the current investigation, Ni-20Cr alloy powder was deposited on SA 516 boiler steel (0.19C-1.07Mn-0.020S-0.25P-0.010Si-balance Fe) by cold spray process. Oxidation kinetics was established for the uncoated and cold spray Ni-20Cr coated boiler steel in an aggressive environment of Na₂SO₄-60%V₂O₅ at 900 °C for 50 cycles by the weight change technique. X-ray diffraction, FE-SEM/EDAX, and x-ray mapping techniques were used to analyze the oxidation products. Uncoated steel suffered corrosion in the form of intense spalling and peeling of its oxide scale, which may be due to the formation of unprotective Fe₂O₃ oxides. The Ni-20Cr coating was successful in reducing the weight gain of the steel by 87.2% which may be due to the formation of oxides of nickel and chromium.     

Cadmium removal out of human plasma using ion-imprinted beads in a magnetic column

The aim of this study is to utilize ion-imprinted magnetic beads in the selective removal of Cd²⁺ ions out of human plasma overdosed with Cd²⁺ ions. The Cd²⁺ imprinted magnetic poly(HEMA-MAC) (mPHEMAC-Cd²⁺) beads were produced by suspension polymerization in the presence of magnetite Fe₃O₄ in a nano-powder form. The template Cd²⁺ ions could be reversibly detached from the matrix to form mPHEMAC-Cd²⁺ beads using 0.1 M thiourea solution. The specific surface area of the mPHEMAC-Cd²⁺ beads was found to be 24.7 m²/g. The MAC and Fe₃O₄ contents of the mPHEMAC-Cd²⁺ beads were found to be 41.8 µmol/g polymer and 8.2% on the average. The Cd²⁺ adsorption capacity of mPHEMAC-Cd²⁺ columns decreased drastically from 48.8 µmol/g to 20.0 µmol/g as the flow rate is increased from 0.50 ml/min to 3.0 ml/min. The maximum adsorption capacity of the mPHEMAC-Cd²⁺ beads was determined to be 48.8 µmol Cd²⁺/g on the average. The relative selectivity coefficients of the mPHEMAC beads for Cd²⁺/Pb²⁺ and Cd²⁺/Zn²⁺ were 22.6 and 160.7 times greater than those of the non-imprinted magnetic PHEMAC (mPHEMAC) beads, respectively. The mPHEMAC-Cd²⁺ beads are reusable for many times with no significant decrease in their adsorption capacities.     

Characterization and In Vitro Corrosion Investigations of Thermal Sprayed Hydroxyapatite and Hydroxyapatite-Titania Coatings on Ti Alloy

In the current investigation, hydroxyapatite (HA) powder was mixed with titania (TiO₂) in 50:50?wt?pct for depositing composite coatings on a Ti-alloy substrate using a thermal-spray coating technique. The coatings were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM)/energy-dispersive X-ray spectroscopy (EDS) analyses. The corrosion behavior of the coatings was studied by electrochemical corrosion testing in simulated human body fluid. After the corrosion testing, the samples were analyzed by XRD and SEM/EDS analyses. HA and TiO₂ (rutile) were the main phases observed in the developed coatings. Bulk HA coating was amorphous; however, the addition of TiO₂ effectively improved the crystallinity of HA in HA-TiO₂ coating. The SEM analysis confirmed the formation of a well-formed HA-TiO₂ composite coating. HA coating exhibited higher bond strength (67.8?MPa) compared with HA-TiO₂ composite coating (37.6?MPa). The electrochemical study showed a significant improvement in the corrosion resistance of the Ti alloy after the deposition of the coatings.     

Review of materials used in laser-aided additive manufacturing processes to produce metallic products

Rapid prototyping (RP) or layered manufacturing (LM) technologies have been extensively used to manufacture prototypes composed mainly of plastics, polymers, paper, and wax due to the short product development time and low costs of these technologies. However, such technologies, with the exception of selective laser melting and sintering, are not used to fabricate metallic products because of the resulting poor life, short cycle, poor surface finish, and low structural integrity of the fabricated parts. The properties endowed by these parts do not match those of functional parts. Therefore, extensive research has been conducted to develop new additive manufacturing (AM) technologies by extending existing RP technologies. Several AM technologies have been developed for the fabrication of metallic objects. These technologies utilize materials, such as Ni-, Al-, and Ti-based alloys and stainless steel powders, to fabricate high-quality functional components. The present work reviews the type of materials used in laser-based AM processes for the manufacture of metallic products. The advantages and disadvantages of processes and different materials are summarized, and future research directions are discussed in the final section. This review can help experts select the ideal type of process or technology for the manufacturing of elements composed of a given alloy or material (Ni, Ti, Al, Pb, and stainless steel).     

Immunoglobulin G recognition with Fab fragments imprinted monolithic cryogels: Evaluation of the effects of metal-ion assisted-coordination of template molecule

In this study, we applied the epitope imprinting approach to prepare molecularly imprinted monolithic cryogels for immunoglobulin G (IgG) recognition. In this respect, we imprinted F_ab fragments of IgG molecules instead of intact protein molecules via two different non-covalent interactions. In the first approach, we directly coordinated F_ab fragments with N-methacryloyl-L-histidine (MAH), polymerizable derivative of L-histidine, but for the second, we used cupric ions [Cu(II)] as mediator between MAH and F_ab fragments. The monolithic cryogels were characterized by Fourier transform infrared (FTIR) spectroscopy, swelling test, and scanning electron microscopy. Then, the monolithic cryogels were used for F_ab fragment adsorption from aqueous solution while evaluating the factors such as pH and F_ab fragment concentration affecting on adsorption process in continuous set-up. After that, monolithic cryogels were used for IgG adsorption by varying pH, IgG concentration, flowrate, and temperature in appropriate ranges. Maximum IgG adsorption capacities were determined as 32.4 mg/g and 49.0 mg/g for directly coordinated cryogel (MIP_Direct) and Cu(II) assisted cryogel (MIP_{Cu(II) assisted}), respectively. Non-imprinted monolithic cryogels were also prepared for control purposes. In addition to F_ab fragments and IgG molecules, albumin and F_c fragment of IgG molecules were used as competitor biomolecules in order to investigate the selectivity gained by imprinting process. Relative selectivity constants were calculated as 1.47, 2.64 and 3.89 for MIP_Direct and 2.90, 8.98, and 11.51 for MIP_{Cu(II) assisted} for F_ab/IgG, F_ab/F_c, and F_ab/albumin as biomolecule pairs, respectively. The desorption efficiency and reusability of MIP_{Cu(II) assisted} cryogel were better than that of MIP_Direct. The results reported here showed that the metal ion assistance improved the selectivity features of the imprinted cryogels and allowed to study under milder conditions with enhanced adsorptive properties.     

Mercury regulation, fate, transport, transformation, and abatement within cement manufacturing facilities: review

The USEPA's 2010 mercury rule, which would reduce emissions from non-hazardous waste burning cement manufacturing facilities by an estimated 94%, represents a substantial regulatory challenge for the industry. These regulations, based on the performance of facilities that benefit from low concentrations of mercury in their feedstock and fuel inputs (e.g., limestone concentration was less than 25 ppb at each facility), will require non-compliant facilities to develop innovative controls. Control development is difficult because each facility's emissions must be assessed and simple correlation to mercury concentrations in limestone or an assumption of ‘typically observed’ mercury concentrations in inputs are unsupported by available data. Furthermore, atmospheric emissions are highly variable due to an internal control mechanism that captures and loops mercury between the high-temperature kiln and low-temperature raw materials mill. Two models have been reported to predict emissions; however, they have not been benchmarked against data from the internal components that capture mercury and do not distinguish between mercury species, which have different sorption and desorption properties. Control strategies include technologies applied from other industries and technologies developed specifically for cement facilities. Reported technologies, listed from highest to lowest anticipated mercury removal, include purge of collected dust or raw meal, changes in feedstocks and fuels, wet scrubbing, cleaning of mercury enriched dust, dry sorbent injection, and dry and semi-dry scrubbing. The effectiveness of these technologies is limited by an inadequate understanding of sorption, desorption, and mercury species involved in internal loop mercury control. To comply with the mercury rule and to improve current mercury control technologies and practices, research is needed to advance fundamental knowledge regarding mercury species sorption and desorption dynamics on materials within cement facilities.