Inorganic-organic phase arrangement as a factor affecting gas-phase desulfurization on catalytic carbonaceous adsorbents

Dried sewage sludge was physically mixed with waste paper (paper-to-sludge ratios from 25% to 75%). To increase the catalytic activity, from 1% to 6% calcium hydroxide was added to the mixtures. Then the precursors were carbonized at 950 degrees C. The performance of materials as H2S adsorbents was tested using a home-developed dynamic breakthrough test. The samples, before and after the adsorption process, were characterized by adsorption of nitrogen, potentiometric titration, thermal analysis, XRF, and SEM. Differences in the performance were linked to the surface properties. Itwas found that mixing paper with sludge increases the amount of H2S adsorbed/oxidized in comparison with that adsorbed/oxidized by the adsorbents obtained from pure precursors (sludge or waste paper) and the capacity is comparable to those of the best activated carbons existing on the market. Although both sewage sludge and waste paper provide the catalytic centers for hydrogen sulfide oxidation, the dispersion of the catalyst and its location within accessible pores is an important factor. The presence of cellulose in the precursor mixture leads to the formation of a light macroporous char whose particles physically separate the inorganic catalytic phase of the sewage sludge origin, decreasing the density of the adsorbent and thus providing more space for storage of oxidation products. This, along with calcium, contributes to a significant increase in the capacity of the materials as hydrogen sulfide adsorbents. On their surface about 30 wt % H2S can be adsorbed, mainly as elemental sulfur or sulfates. The results demonstrate the importance of the composition and arrangement of inorganic/ organic phases for the removal of hydrogen sulfide. The interesting finding is that although some microporosity is necessary to increase the storage area for oxidation products, the carbonaceous phase does not need to be highly microporous. It is important that it provides space for deposition of sulfur, which is formed on the inorganic-phase catalyst. That space can be in meso- and macropores as shown in the case of char derived from the waste paper.     

Anticandidal activity of cobalt containing sunflower oil‐based polymer

Bioactive metal cobalt containing sunflower oil‐based polyesteramide resin was developed by condensation polymerization reaction among oil‐derived sunflower fatty amide diol, adipic acid, and cobalt chloride. Microwave‐assisted synthesis was used throughout the reaction as it enhances reaction rate, gives higher yield, and greater purity of the products. Spectroscopic techniques, such as Fourier transform infrared spectroscopy and proton‐nuclear magnetic resonance, have been used to establish the structure of the polymers. Presence of cobalt in polymer has been confirmed through atomic absorption spectroscopy. Standard laboratory methods such as acid value, hydroxyl value, saponification value, iodine value, specific gravity, and viscosity were used to study the physicochemical characteristics of the polymers. Thermal behavior of the polymer was analyzed using thermogravimetry/differential thermal analysis. The synthesized polymers were evaluated for their biological activity. This study indicates that the synthesized polymer has significant antifungal activity against Candida, including azole‐resistant strains, advocating further investigation for clinical applications in the treatment of fungal infections. POLYM. ENG. SCI., 53:2650–2658, 2013. © 2013 Society of Plastics Engineers     

可降解血管支架用Mg-4.0Zn-0.2Mn-0.2Ca微细管的体外降解行为

通过浸泡实验和电化学测试研究了Mg-4.0Zn-0.2Mn-0.2Ca（质量分数）微细管的体外降解行为与腐蚀机理。结果表明,退火处理可以提高微细管的耐腐蚀性。长期浸泡实验表明腐蚀过程相对均匀,退火微细管在Hank''s溶液中的腐蚀速率约为0.30 mm/a。在浸泡初期,退火管材表面生成Mg(OH)₂,形成保护膜,阻碍腐蚀进行。虽然Mg(OH)₂膜上形成的羟基磷灰石（HA）可以进一步降低腐蚀速率,但是镁基体中粗大的第二相会增强电偶腐蚀效应,并且生成的大量氢气,从而破坏HA膜,使腐蚀继续进行。     

Technical and Economical Aspects of Current Thermal Barrier Coating Systems for Gas Turbine Engines by Thermal Spray and EBPVD: A Review

The most advanced thermal barrier coating (TBC) systems for aircraft engine and power generation hot section components consist of electron beam physical vapor deposition (EBPVD) applied yttria-stabilized zirconia and platinum modified diffusion aluminide bond coating. Thermally sprayed ceramic and MCrAlY bond coatings, however, are still used extensively for combustors and power generation blades and vanes. This article highlights the key features of plasma spray and HVOF, diffusion aluminizing, and EBPVD coating processes. The coating characteristics of thermally sprayed MCrAlY bond coat as well as low density and dense vertically cracked (DVC) Zircoat TBC are described. Essential features of a typical EBPVD TBC coating system, consisting of a diffusion aluminide and a columnar TBC, are also presented. The major coating cost elements such as material, equipment and processing are explained for the different technologies, with a performance and cost comparison given for selected examples.     

Highly selective ion-imprinted particles for solid-phase extraction of Pb ions

The Pb²⁺-imprinted (PHEMAC-Pb²⁺) particles were prepared by bulk polymerization as a solid-phase extraction (SPE) adsorbent. N-methacryloyl-(l)-cysteine (MAC) was used as functional monomer to have a well-shaped molecular geometry between MAC monomer and Pb²⁺ ions that provide molecular recognition based on well fitted cavities for Pb²⁺ ions after removal of template ions. The PHEMAC-Pb²⁺ particles were characterized and the applicability of these particles was investigated for the solid-phase extraction of Pb²⁺ ions from aqueous solutions and environmental samples. The PHEMAC-Pb²⁺ particles with a size range of 50–200 µm have a rough surface and macropores in bulk structure. The adsorption capacity of the PHEMAC-Pb²⁺ particles is relatively low (2.01 mg/g). However, the high selectivity towards competitive ions (Cd²⁺, Ni²⁺ and Cu²⁺) promises the PHEMAC-Pb²⁺ particles an alternative SPE adsorbent in literature. The relative selectivity coefficients of PHEMAC-Pb²⁺ particles for Pb²⁺/Ni²⁺, Pb²⁺/Cd²⁺ and Pb²⁺/Cu²⁺ were almost 71, 117 and 192 times greater than that of non-imprinted (PHEMAC) particles, respectively. Moreover, the reusability of the PHEMAC-Pb²⁺ particles was tested for several times and no significant loss in adsorption capacity was observed. The accuracy of the proposed procedure was also verified by the determination of Pb²⁺ ions in the certified reference material, LGC 6137 Estuarine sediment.     

Adsorption of blood proteins on glow‐discharge‐modified polyurethane membranes

Polyurethanes are a class of polymers that have a wide range of applications in the medical field although their blood compatibility still needs improvement. In order to obtain medical purity, this study prepared membrane‐form polyurethanes from toluene 2,4‐diisocyanate (TDI) and poly(propylene ethylene glycol) without the addition of any ingredients such as solvents, catalysts, or chain extenders. The aim was to increase surface hydrophilicity and improve blood compatibility. Therefore, the prepared membranes were modified by treatment with oxygen or argon plasmas. Characterizations of the samples were achieved by contact‐angle and water‐uptake studies as well as from atomic force microscope (AFM) pictures. It was found that oxygen‐modified samples were more hydrophilic than argon‐modified samples. The AFM images showed that surface roughness increased with plasma treatment. The protein adsorption experiments carried out with single protein solutions demonstrated that the adsorption of bovine serum albumin and fibrinogen decreased drastically by increasing the applied power and exposure time of the glow discharge. A similar decrease in the adsorption of protein was also observed for human blood proteins. The alterations of the conformational structures of the adsorbed proteins were examined by fluorescence spectrophotometry. Similar spectra with the same maximum wavelength were observed for native and desorbed proteins. These results showed that no denaturation of the proteins occurred upon adsorption on the surfaces of the prepared membranes. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 1322–1332, 2001     

Scheduling and sequencing of rubber compounds on banbury mixers in a tyre company

Scheduling and sequencing compounds on banbury mixers is a daily production planning function in a tyre company. The current scheduling procedures are based on experience. A number of factors, such as, capacity, cost, time, speed, set-up of mixers, compound changeovers, density and demand of compound, have to be considered during planning. In this paper, we propose a two-stage approach to this problem. This approach can be easily computerised to aid the personnel in the planning function. An example, considering actual data obtained from the company, is used to illustrate the approach. The current scheduling practice by company personnel, as inferred from past record, is also reported.     

Flow time analyses of a simulated flexible job shop by considering jockeying

It has been essential to include flexibility in manufacturing policy making since variability in demand and products are considerably increasing. However, it is important to know and to monitor the proper level and type of flexibility that is required to obtain full benefits from it. This paper analyses the effects of flexibility on flow time performance of a simulated job shop. For that purpose, several scenarios are developed under four flexibility levels with two different machine selection rule and three types of dispatching rules. Furthermore, effect of jockeying as a queuing policy on the flow time performance is also investigated through simulation modeling. Results indicated that full flexibility is a preferable state for most of the cases. However, in some cases, chain configurations perform similar results since it combines the benefits of pooling and specialization. In addition, it is observed that a queue control mechanism like jockeying is an effective way to improve performance even though it may increase complexity of controlling policy.     

Combining molecular imprinted nanoparticles with surface plasmon resonance nanosensor for chloramphenicol detection in honey

The focus of this article is to develop a surface plasmon resonance (SPR) nanosensor to determine chloramphenicol (CAP) using the molecularly imprinted nanoparticles. The CAP imprinted nanoparticles were prepared by miniemulsion polymerization method. Then, the nanoparticles were attached onto the SPR nanosensor surface via temperature‐controlled evaporation. Surface characterization studies were performed with atomic force microscopy and contact angle measurements. Kinetic studies were performed with CAP solutions in the concentration range of 0.155–6.192 nM. Florphenicol (FLP) and thiamphenicol (TAP) having similar chemical structures to the template (i.e., CAP) were chosen as competitors to determine selectivity of the nanoparticles. Selectivity constants were observed as 8.86 for CAP/TAP and 8.36 for CAP/FLP. The detection limit was calculated as 40 ng/kg honey sample. In the light of these results, it was emphasized that the SPR nanosensor is able to recognize CAP selectively and has a potential for real‐time CAP detection in honey sample. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Dye‐affinity hollow‐fibres and their lysozyme adsorption–desorption characteristics

Dye‐affinity adsorption is increasingly used for protein separation. Hollow‐fibres have advantages as adsorbents in comparison to conventional bead supports because they are not compressible and can eliminate internal diffusion limitations. The aim of this study was to explore in detail the performance of polyamide hollow‐fibres to which Reactive Green HE‐4BD was attached for adsorption of lysozyme. The hollow‐fibre was characterized by scanning electron microscopy. These dye‐carrying hollow‐fibres (26.3 µmol g^?1) were used in the lysozyme adsorption–elution studies. The effect of initial concentration of lysozyme and medium pH on the adsorption efficiency of dye‐attached hollow‐fibres was studied in a batch system. The non‐specific adsorption of lysozyme on the polyamide hollow‐fibres was 1.8 mg g^?1. Reactive Green HE‐4BD attachment significantly increased the lysozyme adsorption up to 41.1 mg g^?1. Langmuir adsorption model was found to be applicable in interpreting lead adsorption by Reactive Green HE‐4BD attached hollow fibres. Significant amount of the adsorbed lysozyme (up to 95%) was eluted in 1 h in the elution medium containing 1.0 M NaSCN at pH 8.0. In order to determine the effects of adsorption conditions on possible conformational changes of lysozyme structure, fluorescence spectrophotometry was employed. We concluded that polyamide dye‐affinity hollow‐fibres can be applied for lysozyme adsorption without causing any significant conformational changes. Repeated adsorption–elution processes showed that these dye‐attached hollow‐fibres are suitable for lysozyme adsorption. © 2001 Society of Chemical Industry