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Artykuły w czasopismach na temat "Novel Nanoporous Organic Materials"

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Shimojima, Atsushi, i Kazuyuki Kuroda. "Alkoxy- and Silanol-Functionalized Cage-Type Oligosiloxanes as Molecular Building Blocks to Construct Nanoporous Materials". Molecules 25, nr 3 (25.01.2020): 524. http://dx.doi.org/10.3390/molecules25030524.

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Siloxane-based materials have a wide range of applications. Cage-type oligosiloxanes have attracted significant attention as molecular building blocks to construct novel siloxane-based nanoporous materials with promising applications such as in catalysis and adsorption. This paper reviews recent progress in the preparation of siloxane-based nanoporous materials using alkoxy- and silanol-functionalized cage siloxanes. The arrangement of cage siloxanes units is controlled by various methods, including amphiphilic self-assembly, hydrogen bonding of silanol groups, and regioselective functionalization, toward the preparation of ordered nanoporous siloxane-based materials.
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Sarkisov, Lev, Tina Düren i Randall Q. Snurr. "Molecular modelling of adsorption in novel nanoporous metal–organic materials". Molecular Physics 102, nr 2 (20.01.2004): 211–21. http://dx.doi.org/10.1080/00268970310001654854.

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Sarkisov, Lev, Tina Düren i Randall Q. Snurr. "Molecular modelling of adsorption in novel nanoporous metal-organic materials". Molecular Physics -1, nr 1 (1.01.2003): 1. http://dx.doi.org/10.1080/00268970410001654854.

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Xiao, Heting, Hebin Jiang, Haixia Yin i Yueting Sun. "Nanofluidic Attenuation of Metal-Organic Frameworks". INTER-NOISE and NOISE-CON Congress and Conference Proceedings 265, nr 1 (1.02.2023): 6314–21. http://dx.doi.org/10.3397/in_2022_0938.

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Porous materials with energy absorption characteristics have been used for attenuation against hazardous vibrations and noises. The intrusion of liquid water and aqueous solutions into hydrophobic nanoporous materials such as metal-organic frameworks (MOFs) present an attractive pathway to engineering new attenuation technologies. In this process, hydrostatic pressure forces water to intrude hydrophobic nanopores, thereby converting mechanical work into interfacial energy through nanoscale interfacial interactions. Once the external pressure is removed, water molecules can flow out of the nanopores spontaneously, making the system reversible. We envision that this mechanism has the potential of innovating attenuation technologies, so in this work we provided a preliminary study in this direction. We investigated a material system consisting of water and a commonly used MOF, zeolitic imidazolate framework-8 (ZIF-8), and demonstrated its reversibility and stability under cyclic pressurization, considered its performance at various peak pressures and frequencies, its tunability in terms of intrusion pressure, and its potential in hydrogel forms. These features are important for potential attenuation technologies based on this novel mechanism.
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Zhang, Lu, Yuan Liu, Han Song, Bintong Huang, Bang-Ce Ye i Yingchun Li. "Nanoporous gold leaf as a signal amplification agent for the detection of VOCs with a quartz crystal microbalance". Analyst 141, nr 15 (2016): 4625–31. http://dx.doi.org/10.1039/c6an00556j.

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In this work, a novel sensing framework coupling nanoporous gold leaf (NPGL) and sensitive materials on a quartz crystal microbalance (QCM) sensor was developed for detection of volatile organic compounds (VOCs).
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Wijaya, Karna, Eddy Heraldy, Lukman Hakim, Ahmad Suseno, Poedji Loekitowati Hariani, Maisari Utami i Wahyu Dita Saputri. "Synthesis and Application of Nanolayered and Nanoporous Materials". ICS Physical Chemistry 1, nr 1 (6.02.2021): 1. http://dx.doi.org/10.34311/icspc.2021.1.1.1.

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Nanoscale materials are currently an attractive research subject because their properties are in contrast to their macroscopic counterparts. An inert material, such as bulk platinum metal for example, is known to exhibit a catalytic properties when its size is reduced into nanoscale. A stable material can become flammable or combustible, such as aluminum, and isolator material can become a conductor. Many attractive quantum phenomena also arise from reducing a material size into nanoscale dimensions. This review article discusses the concept, synthesis, and characterization of organic and inorganic nanolayered and nanoporous materials; and their application to catalysis and adsorption processes. Past achievements and future perspectives in the field of nanomaterial researches will be discussed as well. Furthermore, in the era of green chemistry, nanomaterials with all their derivatives are also required to have sustainable characteristics, such as biodegradable and renewable; which emphasizes that the development of nanomaterials in the framework of green chemistry should always be a priority. Through the synthesis of novel and functional nanomaterials using natural and local-based materials around us that are environmentally friendly and relatively easy to be obtained, our goal toward the inheritance of a greener world for the future generations is not an impossible dream.
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Isaeva, Vera I., Oleg M. Nefedov i Leonid M. Kustov. "Metal–Organic Frameworks-Based Catalysts for Biomass Processing". Catalysts 8, nr 9 (31.08.2018): 368. http://dx.doi.org/10.3390/catal8090368.

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: Currently, metal–organic frame works (MOFs) as novel hybrid nanoporous materials are a top research interest, including endeavors in heterogeneous catalysis. MOF materials are promising heterogeneous catalytic systems due to their unique characteristics, such as a highly ordered structure, a record high surface area and a compositional diversity, which can be precisely tailored. Very recently, these metal-organic matrices have been proven as promising catalysts for biomass conversion into value-added products. The relevant publications show that the structure of MOFs can contribute essentially to the advanced catalytic performance in processes of biomass refining. This review aims at the consideration of the different ways for the rational design of MOF catalysts for biomass processing. The particular characteristics and peculiarities of the behavior of different MOF based catalytic systems including hybrid nanomaterials and composites will be also discussed by illustrating their outstanding performance with appropriate examples relevant to biomass catalytic processing.
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Vasin, Andrii, Dmytro Kysil, Andriy Rusavsky, Oksana Isaieva, Alexander Zaderko, Alexei Nazarov i Volodymyr Lysenko. "Synthesis and Luminescent Properties of Carbon Nanodots Dispersed in Nanostructured Silicas". Nanomaterials 11, nr 12 (1.12.2021): 3267. http://dx.doi.org/10.3390/nano11123267.

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Luminescent carbon nanoparticles are a relatively new class of luminescent materials that have attracted the increasing interest of chemists, physicists, biologists and engineers. The present review has a particular focus on the synthesis and luminescent properties of carbon nanoparticles dispersed inside nanostructured silica of different natures: oxidized porous silicon, amorphous thin films, nanopowders, and nanoporous sol–gel-derived ceramics. The correlations of processing conditions with emission/excitation spectral properties, relaxation kinetics, and photoluminescence photodegradation behaviors are analyzed. Following the evolution of the photoluminescence (PL) through the “from-bottom-to-up” synthesis procedure, the transformation of molecular-like ultraviolet emission of organic precursor into visible emission of carbon nanoparticles is demonstrated. At the end of the review, a novel method for the synthesis of luminescent and transparent composites, in form of nanoporous silica filled with luminescent carbon nanodots, is presented. A prototype of white light emitting devices, constructed on the basis of such luminophores and violet light emitting diodes, is demonstrated.
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J, Ganesan, Jeyadevi S, Siva Kaylasa Sundari S, Arunjunai Raj M, Pitchaimari G i Vijayakumar CT. "Thermal, mechanical, and electrical properties of difunctional and trifunctional epoxy blends with nanoporous materials". Journal of Elastomers & Plastics 54, nr 3 (10.12.2021): 494–508. http://dx.doi.org/10.1177/00952443211060400.

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In the present study, the aim is to synthesize the particulate nanocomposites with difunctional and trifunctional epoxy blend as matrix and synthesized nanoporous materials as fillers. Organic/inorganic hybrid networks were prepared by the novel solvent free method. Viscoelastic, thermal, and electrical properties of di- and trifunctional epoxy and the effect of different nanoparticles in the particulate nanocomposites have been studied by dynamic mechanical analyzer, thermogravimetry (TGA), and dielectric strength. Epoxy mixed with different compositions of TGPAP and particulate nanocomposites by the addition of different types of nanomaterials shows higher storage modulus than the pure epoxy. The addition of TGPAP and nanofillers decreases the thermal stability of epoxy matrix. The evolved gas analysis (TG-FTIR) was also done in order to study the products formed during degradation. An increase in dielectric strength and impact strength (4%) was also observed in the particulate nanocomposites.
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Liu, Chunqing, Nathaniel Naismith, Lei Fu i James Economy. "Novel nanoporous hybrid organic–inorganic silica containing iminodiethanol chelating groups inside the channel pores". Chem. Commun., nr 15 (2003): 1920–21. http://dx.doi.org/10.1039/b304057g.

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Rozprawy doktorskie na temat "Novel Nanoporous Organic Materials"

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Mangano, Enzo. "Rapid screening of novel nanoporous materials for carbon capture separations". Thesis, University of Edinburgh, 2013. http://hdl.handle.net/1842/9497.

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In this work the experimental results from the rapid screening and ranking of a wide range of novel adsorbents for carbon capture are presented. The samples were tested using the Zero Length Column (ZLC) method which has proved to be an essential tool for the rapid investigation of the equilibrium and kinetic properties of prototype adsorbents. The study was performed on different classes of nanoporous materials developed as part of the EPSRC-funded “Innovative Gas Separations for Carbon Capture” (IGSCC) project. More than 120 novel adsorbents with different key features for post-combustion carbon capture were tested. The classes of materials investigated were: • PIMs (Polymers of Intrinsic Microporosity) • MOFs (Metal - Organic Frameworks) • Mesoporous Silica • Zeolites • Carbons All the samples were tested at experimental conditions close to the ones of a typical flue gas of a fossil fuel power plant: 35 ºC and 0.1 bar of partial pressure of CO2. The results from the ranking of the CO2 capacity of the materials, at the conditions of interest, indicate the Mg and Ni-based MOF samples as the adsorbents with the highest uptake among all the candidates. The best sample shows a CO2 capacity almost double than the benchmark adsorbent, zeolite 13X (provided by UOP). The ranking also shows some of the zeolite adsorbents synthesised as promising materials for carbon capture: uptakes comparable or slightly higher than 13X were obtained for several samples of Rho and Chabazite zeolite. Water stability tests were also performed on the best MOFs and showed a deactivation rate considerably faster for the Mg-based MOFs, proving an expected higher resistance to degradation for the Ni based materials. A focused investigation was also carried out on the diffusion of CO2 in different ionexchanged zeolites Rho samples. The study of these samples, characterised by extremely slow kinetics, extended the use of the ZLC method to very slow diffusional time constants which are very difficult to extract from the traditional long time asymptotic analysis. The results show how the combination of the full saturation and partial loading experiment can provide un-ambiguous diffusional time constants. The diffusivity of CO2 in zeolite Rho samples shows to be strongly influenced by the framework structure as well as the nature and the position of the different cations in the framework. The kinetics of the Na-Cs Rho sample was also measured by the use of the Quantachrome Autosorb-iQ™ volumetric system. To correctly interpret the dynamic response of the instrument modifications were applied to the theoretical model developed by Brandani in 1998 for the analysis of the piezometric method. The analytical solution of the model introduces parameters which allow to account for the real experimental conditions. The results confirm the validity of the methodology in the analysis of slow diffusion processes. In conclusion the advantages offered by the small size of the column and the small amount of sample required proved the ZLC method to be a very useful tool for the rapid ranking of the CO2 capacity of prototype adsorbents. Equilibrium and kinetic measurements were performed on a very wide range of novel nanoporous materials. The most promising and interesting samples were further investigated through the use of the water stability test, the partial loading experiment and the volumetric system. The ZLC technique was also extended to the measurements of systems with very slow kinetics, for which is very difficult to extract reliable diffusional time constants. An improved model for the interpretation of dynamic response curves from a non-ideal piezometric system was developed.
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Liu, Yuanyuan. "DEVELOPMENT OF METAL-ORGANIC FRAMEWORK-BASED NANOPOROUS MATERIALS FOR ADSORPTION APPLICATIONS". Kent State University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=kent1542906215640054.

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Vuong, Gia Thanh. "Synthesis and characterization of nanoporous materials: nanozeolites and metal-organic frameworks". Thesis, Université Laval, 2013. http://www.theses.ulaval.ca/2013/29925/29925.pdf.

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Dans ce travail, deux types de nanomatériaux poreux ont été obtenues: des nanozéolithes et des matériaux à réseau organométallique (MOF). Pour les nanozéolithes, deux nouvelles méthodes de synthèses ont été développé: une méthode à phase unique et une méthode biphasique. Dans la méthode à phase unique, une quantité du gel-zéolithique est ajoutée à une solution de toluène/n-butanol contenant l’agent silylant organosilane. Après 12 heures à 60oC, une phase homogène est obtenue. Ce mélange est traité hydrothermalement pour produire une nanozéolithe fonctionalisée. En revanche, la méthode de synthèse à deux phases, implique l’introduction de l’organosilane mélangé à un solvant organique dans le gel de zéolithe aqueux conduisant ainsi à un mélange biphasique. Après mélange et traitement hydrothermal, des nanozéolithes fonctionalisées par silylation sont obtenu dans la phase organique et de larges cristaux de zéolithes sont obtenus dans la phase aqueuse. En principe, les deux méthodes utilisent l’organosilane pour empêcher la croissance des cristaux. Le solvant organique joue le rôle de dispersant des nanozéolithes fonctionalisées avec l’organosilane à partir de la phase aqueuse, et contrôle le processus de croissance des nanozéolithes. Ces deux méthodes de synthèse sont applicables autant aux zéolithes MFI que FAU, telles que silicatite-1, ZSM-5 et NaY. Elles peuvent être étendues à la synthèse d’autres types de zéolithes. L’activité catalytique de ces nanozéolithes a été évaluée pour le craquage de FCC. Les résultats indiquent que la nanozéolithe de type FAU montre une bonne activité dans cette réaction. Pour l’étude des matériaux à réseau organométallique (MOF), une nouvelle approche a été développé pour la synthèse de MIL-88B en utilisant un cluster neutre de métaux mixtes bimétalliques Fe2Ni(µ3-O). Les clusters occupent les nœuds du réseau MIL-88B à la place du mono-métal Fe3 (µ3-O) avec un anion compensateur. Ce dernier est le cluster formant le réseau du Fe3MIL-88B non-poreux qui est obtenu par la méthode conventionnelle. De ce fait, en absence des anions compensateurs dans la structure, Fe2Ni MIL-88B devient un matériau poreux. De plus, avec la combinaison de la flexibilité de MIL-88B et des métaux mixtes comme nœuds dans le réseau, la porosité peut être contrôlée par échange avec des ligands terminaux du réseau. Ceci nous a permis de moduler d’une manière réversible la porosité de MIL-88B à différents niveaux, ainsi que la surface spécifique et le volume de pores dépendant de taille de ligands échangés. Le mécanisme de synthèse a été aussi étudié pour les matétiaux Fe3-MIL88B et Fe2Ni-MIL88B. Les résultats montrent que pour la synthèse de Fe3-MIL88B, le mono-métal Fe3-MOF-235 est comme le précurseur pour la formation de MIL-88B. Dans le cas d’utilisation de métaux mixtes Fe2Ni(µ3-O), les mono-métal Fe3-MOF-235 est formés en premier lors de la synthèse du métal mixte Fe2Ni-MIL88B. Il est montré que la présence de l’anion FeCl4- est déteminante dans la formation de la phase initiale MOF-235 et dans le succès de la synthèse du MIL-88B mono- ou bimétallique. L’anion FeCl4- est très important pour le succès de la formation de MOF-235. Un mécanisme d’anion médiateur dans la formation de MOF-235 a été suggéré.
In this thesis, two types of nanoporous materials: nanozeolites and metal-organic frameworks were studies. For nanozeolites, two novel methods e.g. single-phase and two-phases were reported for the synthesis of nanozeolites. In the single-phase synthesis method, a proper amount of zeolite gel solution was added to a toluene/n-butanol solution containing an organosilane. After 12 hours at 60oC, a single phase mixture was obtained. This mixture was then subjected to hydrothermal crystallization to produce uniform functionalized nanozeolites. In contrast, the two-phase synthesis method involved the introduction of an organic solvent containing organosilane to the aqueous zeolite gel solution, resulting in a two-phase mixture. Upon mixing and hydrothermal treatment of this mixture, organosilane-functionalized nanozeolites were obtained in the organic phase whereas, large zeolite crystals were found in the aqueous phase. In principle, both methods employed the use of organosilane to inhibit the crystal growth. The organic solvent acted as the medium for the dispersion of nanozeolites functionalized with organosilane from the aqueous phase, which led to the complete halt of the growth process. These two methods were demonstrated to be applicable to the synthesis of MFI and FAU nanozeolites such as silicalite-1 and NaY, and could be applied to the synthesis of other types of zeolites. Catalytic activity of the synthesized nanozeolites was evaluated by the cracking reaction of FCC feed. The result showed that FAU nanozeolites can be good catalysts for the cracking reaction. For the study of the metal-organic frameworks (MOF), a new rational approach was developed for the synthesis of mixed metal MIL-88B metal organic framework based on the use of neutral bimetallic cluster, such as Fe2Ni(µ3-O) cluster. Unlike the conventional negative charged single metal cluster, the use of neutral bimetallic cluster as a framework node avoids the need of compensating anion inside porous MIL-88B system; thus such a bimetallic MIL-88B becomes porous. The flexibility of the mixed metal MIL-88B can be controlled by terminal ligands with different steric hindrance. This allows us to reversibly customize the porosity of MIL-88B structure at three levels of specific surface area as well as the pore volume. Synthesis mechanism was also studied. It was found that the monometallic Fe3-MOF-235 is the precursors to the formation of MIL-88B. MOF-235 comes first then later transforms to Fe3-MIL-88B or acts as seeds for the formation of mixed Fe2Ni-MIL88B. FeCl4- anion is very important to the successful formation of MOF-235. An anion mediated mechanism of the formation of MOF-235 is suggested.
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Sun, Zhengfei Wei Yen. "Novel sol-gel nanoporous materials, nanocomposites and their applications in bioscience /". Philadelphia, Pa. : Drexel University, 2005. http://dspace.library.drexel.edu/handle/1860/556.

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Smith, Helen. "Novel organic materials for photovoltaic devices". Thesis, University of Glasgow, 2014. http://theses.gla.ac.uk/5859/.

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Organic materials offer key advantages over their inorganic counterparts for photovoltaics due to the ability to easily tune the physical properties and develop cheaper, more flexible, photovoltaic devices. This thesis describes the synthesis and characterisation of a variety of compounds from small-molecule to supramolecular and polymeric systems with the potential to be used in organic electronics. Herein is described an optimised synthetic route for the synthesis of two flavins and the synthesis and characterisation of a novel flavin and fluorene polymer. Also described is the synthesis of two novel rotaxane structures with the potential for use in organic field effect transistors. The synthesis of a novel polymer incorporating the naphthalene diimide moiety and a P3HT functionality utilising click methodology is also described. Finally the synthesis of a thiophene based star shaped molecule as electron transporting material is also described along with a flavin based organic dye for use in dye-sensitised solar cells.
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Paxton, G. A. N. "Novel organic materials for gas sensing". Thesis, Cranfield University, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273584.

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Jones, Christopher Lloyd. "Some novel oligothiophene-based materials". Thesis, University of Liverpool, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343689.

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Bae, Tae-Hyun. "Engineering nanoporous materials for application in gas separation membranes". Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/42712.

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The main theme of this dissertation is to engineer nanoporous materials and nanostructured surfaces for applications in gas separation membranes. Tunable methods have been developed to create inorganic hydroxide nanostructures on zeolite surfaces, and used to control the inorganic/polymer interfacial morphology in zeolite/polymer composite membranes. The study of the structure-property relationships in this material system showed that appropriate tuning of the surface modification methods leads to quite promising structural and permeation properties of the membranes made with the modified zeolites. First, a facile solvothermal deposition process was developed to prepare roughened inorganic nanostructures on zeolite pure silica MFI crystal surfaces. The functionalized zeolite crystals resulted in high-quality ̒mixed matrix̕ membranes, wherein the zeolite crystals were well-adhered to the polymeric matrix. Substantially enhanced gas separation characteristics were observed in mixed matrix membranes containing solvothermally modified MFI crystals. Gas permeation measurements on membranes containing nonporous uncalcined MFI revealed that the performance enhancements were due to significantly enhanced MFI-polymer adhesion and distribution of the MFI crystals. Solvothermal deposition of inorganic nanostructures was successfully applied to aluminosilicate LTA surfaces. Solvothermal treatment of LTA was tuned to deposit smaller/finer Mg(OH)₂ nanostructures, resulting in a more highly roughened zeolite surface. Characterization of particles and mixed matrix membranes revealed that the solvothermally surface-treated LTA particles were promising for application in mixed matrix membranes. Zeolite LTA materials with highly roughened surfaces were also successfully prepared by a new method: the ion-exchange-induced growth of Mg(OH)₂ nanostructures using the zeolite as the source of the Mg²⁺ ions. The size/shape of the inorganic nanostructures was tuned by adjusting several parameters such as the pH of the reagent solution and the amount of magnesium in the substrates and systematic modification of reaction conditions allowed generation of a good candidate for application in mixed matrix membranes. Zeolite/polymer adhesion properties in mixed matrix membranes were improved after the surface treatment compared to the untreated bare LTA. Surface modified zeolite 5A/6FDA-DAM mixed matrix membranes showed significant enhancement in CO₂ permeability with slight increases in CO₂/CH₄ selectivity as compared to the pure polymer membrane. The CO₂/CH₄ selectivity of the membrane containing surface treated zeolite 5A was much higher than that of membrane with untreated zeolite 5A. In addition, the use of metal organic framework (MOF) materials has been explored in mixed matrix membrane applications. ZIF-90 crystals with submicron and 2-μm sizes were successfully synthesized by a nonsolvent induced crystallization technique. Structural investigation revealed that the ZIF-90 particles synthesized by this method had high crystallinity, microporosity and thermal stability. The ZIF-90 particles showed good adhesion with polymers in mixed matrix membranes without any compatibilization. A significant increase in CO₂ permeability was observed without sacrificing CO₂/CH₄ selectivity when Ultem® and Matrimd® were used as the polymer matrix. In contrast, mixed matrix membranes with the highly permeable polymer 6FDA-DAM showed substantial enhancement in both permeability and selectivity, as the transport properties of the two phases were more closely matched.
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Richards, Gary J. "Novel organic materials for electroluminescent display devices". Thesis, University of Hull, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.342862.

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Haldoupis, Emmanuel. "Mulitscale modeling and screening of nanoporous materials and membranes for separations". Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/47669.

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The very large number of distinct structures that are known for metal-organic frameworks (MOFs) and zeolites presents both an opportunity and a challenge for identifying materials with useful properties for targeted separations. In this thesis we propose a three-stage computational methodology for addressing this issue and comprehensively screening all available nanoporous materials. We introduce efficient pore size calculations as a way of discarding large number of materials, which are unsuitable for a specific separation. Materials identified as having desired geometric characteristics can be further analyzed for their infinite dilution adsorption and diffusion properties by calculating the Henry's constants and activation energy barriers for diffusion. This enables us to calculate membrane selectivity in an unprecedented scale and use these values to generate a small set of materials for which the membrane selectivity can be calculated in detail and at finite loading using well-established computational tools. We display the results of using these methods for >500 MOFs and >160 silica zeolites for spherical adsorbates at first and for small linear molecules such as CO₂ later on. In addition we also demonstrate the size of the group of materials this procedure can be applied to, by performing these calculations, for simple adsorbate molecules, for an existing library of >250,000 hypothetical silica zeolites. Finally, efficient methods are introduced for assessing the role of framework flexibility on molecular diffusion in MOFs that do not require defining a classical forcefield for the MOF. These methods combine ab initio MD of the MOF with classical transition state theory and molecular dynamics simulations of the diffusing molecules. The effects of flexibility are shown to be large for CH₄, but not for CO₂ and other small spherical adsorbates, in ZIF-8.
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Książki na temat "Novel Nanoporous Organic Materials"

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service), SpringerLink (Online, red. Free-Radical Retrograde-Precipitation Polymerization (FRRPP): Novel Concepts, Processes, Materials, and Energy Aspects. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2010.

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Kuzmany, Hans. Electronic Properties of Fullerenes: Proceedings of the International Winterschool on Electronic Properties of Novel Materials, Kirchberg, Tirol, March 6-13, 1993. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993.

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NATO Advanced Research Workshop on Frontiers of High-Pressure Research (2nd 2001 Pingree Park, Colo.). Frontiers of high pressure research II: Application of high pressure to low-dimensional novel electronic materials. Dordrecht: Kluwer Academic Publishers, 2001.

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1940-, Kuzmany H., red. International Winterschool on Electronic Properties of Novel Materials, progress in fullerene research: Kirchberg, Tyrol, Austria, 5-12 March 1994. Singapore: World Scientific, 1994.

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Yan, Mei. Development of New Catalytic Performance of Nanoporous Metals for Organic Reactions. Springer London, Limited, 2014.

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Yan, Mei. Development of New Catalytic Performance of Nanoporous Metals for Organic Reactions. Springer, 2014.

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Yan, Mei. Development of New Catalytic Performance of Nanoporous Metals for Organic Reactions. Springer Japan, 2016.

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Development of New Catalytic Performance of Nanoporous Metals for Organic Reactions. Mei Yan, 2014.

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(Editor), A. K.-Y. Jen, L. R. Dalton (Editor) i M. F. Rubner (Editor), red. Electrical, Optical, and Magnetic Properties of Organic Solid State Materials: Symposium Held Novel 27-December 1, 1995 (Materials Research Society Symposium Proceedings). Materials Research Society, 1996.

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Novel Macromolecular Architectures via a Combination of Cyclodextrin Host/Guest Complexation and RAFT Polymerization. Springer, 2014.

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Części książek na temat "Novel Nanoporous Organic Materials"

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Bon, V., I. Senkovska i S. Kaskel. "Metal-Organic Frameworks". W Nanoporous Materials for Gas Storage, 137–72. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-3504-4_6.

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Ma, Yunsheng, Hideki Tanaka i Ryotaro Matsuda. "CO2 Storage on Metal-Organic Frameworks". W Nanoporous Materials for Gas Storage, 331–58. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-3504-4_12.

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Dailly, Anne, i Matthew Beckner. "Methane Storage on Metal-Organic Frameworks". W Nanoporous Materials for Gas Storage, 227–53. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-3504-4_9.

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Ladik, János J., i Thomas C. Collins. "On the Possibility of High-Temperature Superconductivity in Organic Materials". W Novel Superconductivity, 181–85. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1937-5_19.

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Jiang, Wen Long, Yu Duan, Yi Zhao, Jingying Hou i Shi Yong Liu. "A Novel Efficient Blue Organic Light Emitting Structure". W Materials Science Forum, 3677–80. Stafa: Trans Tech Publications Ltd., 2005. http://dx.doi.org/10.4028/0-87849-960-1.3677.

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Onodera, Tsunenobu, Hitoshi Kasai, Hidetoshi Oikawa i Hachiro Nakanishi. "Fabrication of Organic Nanocrystals and Novel NanoHybrid Materials". W Nanohybridization of Organic-Inorganic Materials, 81–100. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-92233-9_4.

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Dubbeldam, David. "Simulation of Crystalline Nanoporous Materials and the Computation of Adsorption/Diffusion Properties". W Gas Adsorption in Metal-Organic Frameworks, 219–326. Boca Raton, FL : CRC Press/Taylor & Francis Group, [2018]: CRC Press, 2018. http://dx.doi.org/10.1201/9780429469770-6.

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Lu, Weiyi. "Novel Protection Mechanism of Blast and Impact Waves by Using Nanoporous Materials". W Dynamic Behavior of Materials, Volume 1, 177–83. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-22452-7_25.

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Prasad, Paras N., Frank V. Bright, Upvan Narang, Run Wang, Richard A. Dunbar, Jeffrey D. Jordan i Raz Gvishi. "Novel Organic—Inorganic Composite Materials for Photonics". W ACS Symposium Series, 317–30. Washington, DC: American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0585.ch025.

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Gadd, K. F. "Metal-Containing Cellulose: Some Novel Materials". W Inclusion Phenomena in Inorganic, Organic, and Organometallic Hosts, 265–68. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3987-5_46.

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Streszczenia konferencji na temat "Novel Nanoporous Organic Materials"

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Barua, Nirmalay, William T. Winter, Serrita A. McAuley, Paul T. Clarkson, Joshua Prestage, Andrew R. Salmon i Tanya Hutter. "Adsorption of volatile organic compounds inside a nanoporous silica waveguide". W Optics and Photonics for Sensing the Environment. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/es.2022.em1d.3.

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Adsorption in complex nanoporous materials is important for many applications. We report a novel approach for measuring adsorption in situ that uses a nanoporous silica waveguide and near-infrared spectroscopy for selective measurement of adsorbed compounds.
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Parkinson, Bruce, i John Hoberg. "New 2D Nanoporous Covalent Organic Framework Materials with Functionalized". W nanoGe Fall Meeting 2018. València: Fundació Scito, 2018. http://dx.doi.org/10.29363/nanoge.fallmeeting.2018.080.

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Parkinson, Bruce, i John Hoberg. "New 2D Nanoporous Covalent Organic Framework Materials with Functionalized". W nanoGe Fall Meeting 2018. València: Fundació Scito, 2018. http://dx.doi.org/10.29363/nanoge.nfm.2018.080.

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Tuz, A. A., A. K. Şimşek i M. Kazanci. "Production of organic nanoparticles by using nanoporous membranes". W PROCEEDINGS OF THE 6TH INTERNATIONAL ADVANCES IN APPLIED PHYSICS AND MATERIALS SCIENCE CONGRESS & EXHIBITION: (APMAS 2016). Author(s), 2017. http://dx.doi.org/10.1063/1.4975463.

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Levchenko, A. N., A. I. Starikov, O. N. Bezkrovnaya, I. M. Pritula, I. S. Krapivin i V. B. Tyutyunnik. "Electrical properties of SiO2-based nanoporous materials containing organic dyes". W 2016 IEEE 7th International Conference on Advanced Optoelectronics and Lasers (CAOL). IEEE, 2016. http://dx.doi.org/10.1109/caol.2016.7851398.

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Ilin, D. O., N. A. Martemyanov, A. S. Vokhmintsev i I. A. Weinstein. "Comparative Analysis of Photoluminescence Characteristics of Nanoporous Alumina Anodized in Different Electrolytes". W Novel Optical Materials and Applications. Washington, D.C.: OSA, 2018. http://dx.doi.org/10.1364/noma.2018.now1j.3.

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MERIAKRI, V. V., I. P. NIKITIN, M. P. PARKHOMENKO, N. A. FEDOSEEV i KUANG-LIEH LU. "DIELECTRIC PROPERTIES OF NANOPOROUS METAL-ORGANIC FRAMEWORK MATERIALS IN THE MILLIMETER-WAVE BAND". W Proceedings of International Conference Nanomeeting – 2013. WORLD SCIENTIFIC, 2013. http://dx.doi.org/10.1142/9789814460187_0064.

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Guenter, Peter. "Novel High Nonlinearity Organic Crystals". W Nonlinear Optics: Materials, Fundamentals and Applications. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/nlo.1996.nwd.2.

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We will present the most recent results on the growth and characterization of novel high quality molecular crystals for nonlinear optics. These crystals are based on ionic or hydrogen bonding of new and known chromophores with large second-order hyperpolarizabilities. Detailed results of optical, electro-optical and nonlinear-optical properties of high quality and large size DAST crystals, of hydrazone derivatives and new co-crystals will be presented. It will be shown that optimized parallel alignment of chromophores as well as optimum structures for phase-matched frequency mixing have been realized. In addition, we report on the measurement of the highest known phase-matchable nonlinear susceptibility coefficient of 200 pm/v determined recently in our laboratory.
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Armani, Andrea M., Jinghan He, Andre Kovach i Hyungwoo Choi. "Hybrid Organic/Inorganic Integrated Photonics". W Novel Optical Materials and Applications. Washington, D.C.: OSA, 2019. http://dx.doi.org/10.1364/noma.2019.nom2b.2.

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Nguyen, Thuc-Quyen. "Novel materials for organic electrochemical transistors". W Organic and Hybrid Field-Effect Transistors XX, redaktorzy Oana D. Jurchescu i Iain McCulloch. SPIE, 2021. http://dx.doi.org/10.1117/12.2597204.

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Raporty organizacyjne na temat "Novel Nanoporous Organic Materials"

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Laird, Dr Darin, Dr Christine McGuiness i Mark Storch. High Performance Organic Photovoltaics via Novel Materials Combinations. Office of Scientific and Technical Information (OSTI), styczeń 2011. http://dx.doi.org/10.2172/1002150.

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Hu, Bin. Exploring Novel Spintronic Responses from Advanced Functional Organic Materials. Fort Belvoir, VA: Defense Technical Information Center, listopad 2015. http://dx.doi.org/10.21236/ada626817.

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Park, Soo Y., i Jin H. Kim. Exploring Novel Spintronic Responses from Advanced Functional Organic Materials. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2015. http://dx.doi.org/10.21236/ada626929.

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Biefeld, R. M., S. R. Kurtz i A. A. Allerman. Novel materials and device design by metal-organic chemical vapor deposition for use in infrared emitters. Office of Scientific and Technical Information (OSTI), grudzień 1996. http://dx.doi.org/10.2172/414397.

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