Qualitative characterization of healthcare wastes

The biological hazard inherent in the clinical wastes should be considered during the management and treatment process as well as the disposal into the environment. In this chapter, the risks associated with the clinical wastes as well as the management of these wastes are discussed. The chapter focused on reviewing the types of healthcare wastes generated from hospitals and clinics as well as the regulations and management practices used for these wastes. Moreover, the health risk associated with the infectious agents which have the potential to be transmitted into the environment. It has appeared that the clinical wastes represent real hazards for the human health and the environment if they were not managed properly

Highly permeable macroporous polymers synthesized from pickering medium and high internal phase emulsion templates

Open porous poly-Plckerlng-M/HIPEs with permeabilities of up to 2.6 D were prepared by polymerisation of PickeringM/HIPEs to which small amounts of surfactant were added. The permeability of these poly-Pickering-M/HIPEs is more than 5 times that of conventional polyHI PEs. This approach allows the synthesis of a novel class of permeable particle reinforced macroporous polymers with significant potential for practical exploitation. (Figure Presented) © 2010 WILEY-VCH VerlagGmbH S.Co. KCaA, Weinheim

Wavelength dependence of light diffusion in strongly scattering macroporous gallium phosphide

We present time-resolved measurements of light transport through strongly scattering macroporous gallium phosphide at various vacuum wavelengths between 705 nm and 855 nm. Within this range the transport mean free path is strongly wavelength dependent, whereas the observed energy velocity is shown to be independent of the wavelength. We conclude that microscopic resonances, which can strongly slow down the diffusion process in, e.g., granular TiO2, are absent in macroporous gallium phosphide in the wavelength region of concern

Hierarchical Structure with Highly Ordered Macroporous-Mesoporous Metal-Organic Frameworks as Dual Function for CO2 Fixation.

As a major greenhouse gas, the continuous increase of carbon dioxide (CO2) in the atmosphere has caused serious environmental problems, although CO2 is also an abundant, inexpensive, and nontoxic carbon source. Here, we use metal-organic framework (MOF) with highly ordered hierarchical structure as adsorbent and catalyst for chemical fixation of CO2 at atmospheric pressure, and the CO2 can be converted to the formate in excellent yields. Meanwhile, we have successfully integrated highly ordered macroporous and mesoporous structures into MOFs, and the macro-, meso-, and microporous structures have all been presented in one framework. Based on the unique hierarchical pores, high surface area (592 m2/g), and high CO2 adsorption capacity (49.51 cm3/g), the ordered macroporous-mesoporous MOFs possess high activity for chemical fixation of CO2 (yield of 77%). These results provide a promising route of chemical CO2 fixation through MOF materials

Experimental kinetic study of transesterification of ethyl acetate with methanol catalyzed by gel and macroporous acidic ion exchange resins

The reaction kinetics of the liquid-phase transesterification of ethyl acetate with methanol have been investigated over a series of commercially available ion-exchange resins. Two morphology types of cross-linked polymer resins have been considered, i.e., a gel type (Lewatit K1221) and a macroporous type (Lewatit K2640, Lewatit K2629 and Amberlyst 15). The effect of the swelling of the resin, the initial reactant molar ratio (1:1 – 10:1) and the temperature (303.15 – 333.15 K) on the reaction kinetics was experimentally assessed. Lewatit K1221, the gel-type resin, outperformed the macroporous-type resins, despite its similar number of sulfonic acid sites. The resin’s swelling behavior, which can be related to its degree of cross-linking with divinylbenzene, was identified as the key parameter to explain differences in acid site accessibility between the considered resins and, hence, the observed transesterification kinetics. A fundamental kinetic model, accounting for the chemical elementary steps as well as for the physical swelling due to solvent absorption, was constructed to quantitatively assess the experimental observations. According to this model (1) all active sites are occupied by methanol in protonated form, (2) the esters undergo a proton exchange with the protonated methanol and (3) the reaction occurs through an Eley-Rideal mechanism with the surface reaction of protonated ethyl acetate with methanol from the bulk as the rate-determining step. The kinetic model was able to adequately describe the entire experimental data set. An activation energy amounting to 49 kJ mol-1 was obtained, irrespective of the resin. Also the affinity of each of the resins for the esters was found to be similar. The differences in catalytic activity between the considered resins are found back in the values for the rate coefficients and, hence, can be brought into relation with the active site accessibility. The latter is a factor 3 to 4 higher for gel-type resins compared to macroporous-type resins. An independent experimental assessment of the resins’ swelling behavior confirmed the more pronounced swelling of the gel-type compared to the macroporous-type resins

Porous silicon solar cells

We developed a new process for the fabrication of crystalline solar cell, based on an ultrathin silicon membrane, taking advantage of porous silicon technology. The suggested architecture allows the costs reduction of silicon based solar cell reusing the same wafer to produce a great number of membranes. The architectures combines the efficiency of crystalline silicon solar cell, with the great absorption of porous silicon, and with a more efficient way to use the material. The new process faces the main challenge to achieve an effective and not expensive passivation of the porous silicon surface, in order to achieve an efficient photovoltaic device. At the same time the process suggests a smart way to selective doping of the macroporous silicon layers despite the through-going pores. © 2015 IEEE. SciVal Topic Prominence  Topic: Porous silicon | Silicon | macroporous silicon Prominence percentile: 66.984  Author keywords nanofabricationporous siliconsilicon nanoelectronicssolar cells Indexed keywords Engineering controlled terms: Crystalline materialsNanoelectronicsNanostructured materialsNanotechnologyPorous siliconSiliconSilicon wafersSolar cells Engineering uncontrolled terms Crystalline silicon solar cellsCrystalline solar cellsMacro porous siliconPhotovoltaic devicesPorous silicon surfacesPorous silicon technologySilicon nanoelectronicsUltrathin silicon membrane Engineering main heading: Silicon solar cells ISBN: 978-146738155-0 Source Type: Conference Proceeding Original language: English DOI: 10.1109/NANO.2015.7388710 Document Type: Conference Paper Sponsors: Nanotechnology Council Publisher: Institute of Electrical and Electronics Engineers Inc. References (9) View in search results format ▻ All Export  Print  E-mail Save to PDF Create bibliography 1 (2012) International Technology Roadmap for Photovoltaics Results 2012. Cited 24 times. ITRPV, Third Edition, Berlin 2012 www.ITRPV.net 2 Lehmann, V., Honlein, W., Stengl, R., Willer, J., Wendt, H. (1992) Verfahren Zur Herstellung Einer Solarzelle Aus Einer Substratscheibe. Cited 6 times. German patent DE4204455C1; Filing date: 29. 01. 3 Brendel, R., Ernst, M. Macroporous Si as an absorber for thin-film solar cells (2010) Physica Status Solidi - Rapid Research Letters, 4 (1-2), pp. 40-42. Cited 22 times. http://www3.interscience.wiley.com/cgi-bin/fulltext/123215552/PDFSTART doi: 10.1002/pssr.200903372 Locate full-text(opens in a new window) View at Publisher 4 Ernst, M., Brendel, R., Ferré, R., Harder, N.-P. Thin macroporous silicon heterojunction solar cells (2012) Physica Status Solidi - Rapid Research Letters, 6 (5), pp. 187-189. Cited 16 times. doi: 10.1002/pssr.201206113 Locate full-text(opens in a new window) View at Publisher 5 Ernst, M., Brendel, R. Macroporous silicon solar cells with an epitaxial emitter (2013) IEEE Journal of Photovoltaics, 3 (2), art. no. 6472253, pp. 723-729. Cited 7 times. doi: 10.1109/JPHOTOV.2013.2247094 Locate full-text(opens in a new window) View at Publisher 6 Ernst, M., Schulte-Huxel, H., Niepelt, R., Kajari-Schröder, S., Brendel, R. Thin crystalline macroporous silicon solar cells with ion implanted emitter (Open Access) (2013) Energy Procedia, 38, pp. 910-918. Cited 2 times. http://www.sciencedirect.com/science/journal/18766102 doi: 10.1016/j.egypro.2013.07.364 Locate full-text(opens in a new window) View at Publisher 7 Nenzi, P., Kholostov, K., Crescenzi, R., Bondarenka, H., Bondarenko, V., Balucani, M. Electrochemically etched TSV for porous silicon interposer technologies (2013) Proceedings - Electronic Components and Technology Conference, art. no. 6575887, pp. 2201-2207. Cited 2 times. ISBN: 978-147990233-0 doi: 10.1109/ECTC.2013.6575887 Locate full-text(opens in a new window) View at Publisher 8 Perticaroli, S., Varlamava, V., Palma, F. Microwave sensing of nanostructured semiconductor surfaces (2014) Applied Physics Letters, 104 (1), art. no. 013110. Cited 3 times. doi: 10.1063/1.4861424 Locate full-text(opens in a new window) View at Publisher 9 De Cesare, G., Caputo, D., Tucci, M. Electrical properties of ITO/crystalline-silicon contact at different deposition temperatures (2012) IEEE Electron Device Letters, 33 (3), art. no. 6142006, pp. 327-329. Cited 28 times. doi: 10.1109/LED.2011.2180356 Locate full-text(opens in a new window) View at Publisher © Copyright 2017 Elsevier B.V., All rights reserved. ◅ Back to results ◅ Previous 3of10 Next ▻  Top of page Metrics Learn more about article metrics in Scopus (opens in a new window)  0 Citations in Scopus 0 Learn more about Field-Weighted Citation Impact Field-Weighted Citation Impact PlumX Metrics Usage, Captures, Mentions, Social Media and Citations beyond Scopus.  Cited by 0 documents Inform me when this document is cited in Scopus: Set citation alert ▻ Set citation feed ▻ Related documents Thin crystalline macroporous silicon solar cells with ion implanted emitter Ernst, M. , Schulte-Huxel, H. , Niepelt, R. (2013) Energy Procedia Multilayer etching for kerf-free solar cells from macroporous silicon Schäfer, S. , Ernst, M. , Kajari-Schröder, S. (2013) Energy Procedia Macroporous silicon solar cells with an epitaxial emitter Ernst, M. , Brendel, R. (2013) IEEE Journal of Photovoltaics View all related documents based on references Find more related documents in Scopus based on: Authors ▻ Keywords ▻ About Scopus What is Scopus Content coverage Scopus blog Scopus API Privacy matters Language 日本語に切り替える 切换到简体中文 切換到繁體中文 Русский язык Customer Service Help Contact us Elsevier Terms and conditions ↗ Privacy policy ↗ Copyright © 2018 Elsevier B.V ↗. All rights reserved. Scopus® is a registered trademark of Elsevier B.V. We use cookies to help provide and enhance our service and tailor content. By continuing, you agree to the use of cookies. RELX Group We developed a new process for the fabrication of crystalline solar cell, based on an ultrathin silicon membrane, taking advantage of porous silicon technology. The suggested architecture allows the costs reduction of silicon based solar cell reusing the same wafer to produce a great number of membranes. The architectures combines the efficiency of crystalline silicon solar cell, with the great absorption of porous silicon, and with a more efficient way to use the material. The new process faces the main challenge to achieve an effective and not expensive passivation of the porous silicon surface, in order to achieve an efficient photovoltaic device. At the same time the process suggests a smart way to selective doping of the macroporous silicon layers despite the through-going pores

Study of Ni Metallization in Macroporous Si Using Wet Chemistry for Radio Frequency Cross-Talk Isolation in Mixed Signal Integrated Circuits.

A highly conductive moat or Faraday cage of through-the-wafer thickness in Si substrate was proposed to be effective in shielding electromagnetic interference thereby reducing radio frequency (RF) cross-talk in high performance mixed signal integrated circuits. Such a structure was realized by metallization of selected ultra-high-aspect-ratio macroporous regions that were electrochemically etched in p- Si substrates. The metallization process was conducted by means of wet chemistry in an alkaline aqueous solution containing Ni2+ without reducing agent. It is found that at elevated temperature during immersion, Ni2+ was rapidly reduced and deposited into macroporous Si and a conformal metallization of the macropore sidewalls was obtained in a way that the entire porous Si framework was converted to Ni. A conductive moat was as a result incorporated into p- Si substrate. The experimentally measured reduction of crosstalk in this structure is 5~18 dB at frequencies up to 35 GHz

Enhanced surface interaction of water confined in hierarchical porous polymers induced by hydrogen bonding

Hierarchical porous polymer systems are increasingly applied to catalysis, bioengineering, or separation technology because of the versatility provided by the connection of mesopores with percolating macroporous structures. Nuclear magnetic resonance (NMR) is a suitable technique for the study of such systems as it can detect signals stemming from the confined liquid and translate this information into pore size, molecular mobility, and liquid−surface interactions. We focus on the properties of water confined in macroporous polymers of ethylene glycol dimethacrylate and 2-hydroxyethyl methacrylate [poly- (EGDMA-co-HEMA)] with different amounts of cross-linkers, in which a substantial variation of hydroxyl groups is achieved. As soft polymer scaffolds may swell upon saturation with determined liquids, the use of NMR is particularly important as it measures the system in its operational state. This study combines different NMR techniques to obtain information on surface interactions of water with hydrophilic polymer chains. A transition from a surface-induced relaxation in which relaxivity depends on the pore size to a regime where the organic pore surface strongly restricts water diffusion is observed. Surface affinities are defined through the molecular residence times near the network surface.Fil: Silletta, Emilia Victoria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; ArgentinaFil: Velasco, Manuel Isaac. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; ArgentinaFil: Gomez, Cesar Gerardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; ArgentinaFil: Strumia, Miriam Cristina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; ArgentinaFil: Stapf, Siegfried. Technische Universität Ilmenau; AlemaniaFil: Mattea, Carlos. Technische Universität Ilmenau; AlemaniaFil: Monti, Gustavo Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; ArgentinaFil: Acosta, Rodolfo Hector. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentin

Sorption kinetics for the removal of aldehydes from aqueous streams with extractant impregnated resins

The sorption kinetics for the removal aldehydes from aqueous solutions with Amberlite XAD-16 and MPP particles impregnated with Primene JM-T was investigated. A model, accounting for the simultaneous mass transfer and chemical reaction, is developed to describe the process. It is based on the analogy to the diffusion and reaction in a stagnant liquid sphere, but corrected for the porosity and particle properties influencing the diffusion. The developed model describes the kinetic behavior of the process in the low concentration region rather well. However, in the high concentration region, larger discrepancies are observed. Initially, the influence of the flow rate was investigated to eliminate the effect of the external mass transfer. The influence of the particle morphology was investigated for both physical and reactive sorption. Physical sorption experiments were used to determine the factor τ that takes the particle properties influencing the diffusion into account. It was shown that the diffusion is faster in XAD-16 than in MPP impregnated systems. Reaction rate constant kx was determined by fitting the model to the experimental data. Sorption of benzaldehyde appears to be significantly slower (kx ~ 10−4 l/mol s) than the sorption of pentanal (kx ~ 10−3 l/mol s) due to the slower chemical reaction. The influence of the particle size was investigated for the sorption of pentanal with XAD-16. It was observed that the particle size does influence the diffusion term, but does not have an effect on the reaction rate. On the other hand, the extractant loading influences the reaction rate slightly in the low concentration region, whereas the initial concentration of the solute has more pronounced effect