WorldWideScience

Sample records for pvdf-hfp-based porous polymer

  1. PVDF-HFP-based porous polymer electrolyte membranes for lithium-ion batteries

    DEFF Research Database (Denmark)

    Miao, Ruiying; Liu, Bowen; Zhu, Zhongzheng

    2008-01-01

    As a potential electrolyte for lithium-ion batteries, a porous polymer electrolyte membrane based on poly(vinylidenefluoride-hexafluoropropylene) (PVDF-HFP) was prepared by a phase inversion method. The casting solution, effects of the solvent and non-solvent and addition of micron scale TiO2 par...

  2. PVDF-HFP-based porous polymer electrolyte membranes for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Miao, Ruiying; Liu, Bowen; Zhu, Zhongzheng; Liu, Yun; Li, Jianling; Wang, Xindong [Department of Physical Chemistry, University of Science and Technology Beijing, Beijing 100083 (China); Li, Qingfeng [Department of Chemistry, Technology University of Denmark, DK-2800 Lyngby (Denmark)

    2008-10-01

    As a potential electrolyte for lithium-ion batteries, a porous polymer electrolyte membrane based on poly(vinylidenefluoride-hexafluoropropylene) (PVDF-HFP) was prepared by a phase inversion method. The casting solution, effects of the solvent and non-solvent and addition of micron scale TiO{sub 2} particles were investigated. The membranes were characterized by SEM, XRD, AC impedance, and charge/discharge tests. By using acetone as the solvent and water as the non-solvent, the prepared membranes showed good ability to absorb and retain the lithium ion containing electrolyte. Addition of micron TiO{sub 2} particles to the polymer electrolyte was found to enhance the tensile strength, electrolyte uptake, ion conductivity and the electrolyte/electrode interfacial stability of the membrane. (author)

  3. Ionic transport and electrochemical stability of PVDF-HFP based gel polymer electrolytes

    Science.gov (United States)

    Rosdi, A.; Zainol, N. H.; Osman, Z.

    2016-02-01

    The gel polymer electrolytes (GPEs) samples consisting of polyvinylidenefluoride-co-hexafluoropropylene (PVDF-HFP), ethylene carbonate (EC) and propylene carbonate (PC) with different concentrations of magnesium triflate salt, Mg(CF3SO3)2 were prepared using the solution casting technique. The ionic conductivity of the GPEs was studied by using a.c impedance spectroscopy and the sample containing 20 wt% salt exhibited the highest conductivity of 5.11 × l0-3 Scm-1. Ionic transport number of the GPEs shows that the samples contain ionic species as main charge carrier while cationic transport number for the highest conducting sample was found to be 0.27. The electrochemical properties of the GPEs were studied using Linear Sweep Voltammetry (LSV) and Cyclic Voltammetry (CV). The GPEs show high electrochemical stability ˜3.5V (versus Mg2+/Mg) where the highest conducting sample exhibited the highest stability.

  4. 添加TiO2的聚合物电解质膜PVDF-HFP的性能研究%Properties of the PVDF-HFP based polymer electrolyte membrane filled with TiO2 nanoparticles

    Institute of Scientific and Technical Information of China (English)

    李琪; 芮含笑; 乔庆东

    2012-01-01

    通过添加不同质量分数的TiO2纳米粒子制备多孔聚合物电解质膜PVDF-HFP,制备的聚合物电解质膜通过红外,交流阻抗,线性伏安扫描、首次充放电测试等方法进行了性能测试.添加TiO2纳米填料后,降低了聚合物链的结晶度和极性,当填料的质量分数为8%时,表现出较好的电化学性能,吸液率为184%,孔隙率为93%,室温电导率达到2.05×10-3 S/cm,电化学稳定窗口为4.7V,能满足要求.%Various amounts of nanoscale rutile Ti()2 particle were used as fillers in the preparation of poly(vinylidenefluoride-hexafluoropropylene) (PVDF-HFP) based porous polymer electrolytes. The structure was investigated through FT-IR, the ionic conductivity was determined by AC impedance method, the electrochemical stability was measured by linear scan voltammetry experiment, and the charge-discharge of the polymer lithium batteries based on this composite gel polymer electrolyte was investigated. The polarity of CF2 groups in the polymer chains and the crystallinity of the polymer e-lectrolytes decreased after the addition of TiC>2 nanoparticles. When the composite polymer film contained 8% of Ti()2 nanoparticles, the polymer electrolytes exhibited excellent physico-chemical properties and electrochemical properties such as liquid uptake of 184%,porosity of 93%,high ionic conductivity, up to 2. 05 X 10 * S/cm at room temperature,and electrochemical window of 4. 7 V. It is suitable for practical use.

  5. MICROPOROUS PVDF-HFP-BASED POLYMER MEMBRANES FORMED FROM SUPERCRITICAL CO2 INDUCED PHASE SEPARATION

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Microporous poly(vinylidene fluoride-co-hexafluoropropylene)(PVDF-HFP)membranes following supercritical CO2 induced phase separation process were prepared using four solvents.The solid electrolytes of PVDF-HFP were formed by microporous PVDF-HFP membranes filled and swollen by a liquid electrolyte.The effect of the solvents on the morphology and structure,electrolyte absorptions and lithium ionic conductivity of the activated membranes were investigated.It was approved that all the membrane had the similar"sponge-like"and asymmetric structure when different solvent was used.As the mutual affinity between solvent and supercritical CO2 decreased,the membrane porosity and the average pore diameter increased.The PVDF-HFP membrane with porosity at 88% and pore size at 10 μm were successfully prepared.The uptake of electrolyte solution and lithium ionic conductivity could reach 487 wt% and 3.09×10-3 S/cm respectively for obtained membrane.

  6. PVDF-HFP基聚合物电解质膜的制备及性能表征%Preparation and characterization of PVDF-HFP-based polymer electrolyte

    Institute of Scientific and Technical Information of China (English)

    刘伯文; 王新东; 李建玲; 郭敏

    2009-01-01

    采用相转化法制备了PVDF-HFP基多孔聚合物电解质,研究了PVDF-HFP的溶解温度、溶剂用量以及非溶剂用量等因素对聚合物电解质性能的影响,分别采用交流阻抗法和稳态电流法测定了聚合物电解质膜的离子电导率和离子迁移数,并通过扫描电镜观察了多孔聚合物膜的表面形貌,研究表明,制备PVDF-HFP多孔聚合物电解质膜的合适条件为:溶胶温度50~60℃、溶胶时间2 h、溶剂与PVDF的质量比为9~11、非溶剂与PVDF的质量比为0.5~0.25.该条件下制得的多孔聚合物电解质膜的孔隙率达到70%左右、离子迁移数在0.3左右、室温离子电导率达到1.6×10-3 S·cm-1.

  7. Increased charge transfer of PVDF-HFP based electrolyte by addition of graphite nanofiber and its application in dye-sensitized solar cells

    Science.gov (United States)

    Zhao, Xing Guan; Jin, En Mei; Gu, Hal-Bon

    2013-12-01

    The PEO and PVDF-HFP mixtures were used as polymer electrolytes in solid-state dye-sensitized solar cells (DSSCs). Correlation between the ionic conductivity and cell performance by varying the composition of polymer electrolytes was investigated to elucidate the importance of the ionic conductivity in determining the charge transfer and energy conversion efficiency of solid-state DSSCs. In this work, for increasing the ionic conductivity and charge transfer, GNF was added to the polymer electrolyte. The ionic conductivity of polymer electrolyte containing GNF (0.005 g) is 8.67 × 10-4 S cm-1 and pristine polymer electrolyte is 3.81 × 10-4 S cm-1. The charge transfer of GNF (0.005 g) added DSSCs is faster than the other samples, the electron transport time is 1.53 ms and electron life time is 27.20 ms. The increase of current density with the polymer electrolyte containing GNF (0.005 g) can be possibly attributed to the direct contact between dye/TiO2 and I/I3- that will improve the charge transportation. The highest energy conversion efficiency of 4.60% is obtained for polymer electrolyte containing GNF (0.005 g).

  8. Increased charge transfer of PVDF-HFP based electrolyte by addition of graphite nanofiber and its application in dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Xing Guan; Jin, En Mei; Gu, Hal-Bon, E-mail: hbgu@chonnam.ac.kr

    2013-12-15

    The PEO and PVDF-HFP mixtures were used as polymer electrolytes in solid-state dye-sensitized solar cells (DSSCs). Correlation between the ionic conductivity and cell performance by varying the composition of polymer electrolytes was investigated to elucidate the importance of the ionic conductivity in determining the charge transfer and energy conversion efficiency of solid-state DSSCs. In this work, for increasing the ionic conductivity and charge transfer, GNF was added to the polymer electrolyte. The ionic conductivity of polymer electrolyte containing GNF (0.005 g) is 8.67 × 10{sup −4} S cm{sup −1} and pristine polymer electrolyte is 3.81 × 10{sup −4} S cm{sup −1}. The charge transfer of GNF (0.005 g) added DSSCs is faster than the other samples, the electron transport time is 1.53 ms and electron life time is 27.20 ms. The increase of current density with the polymer electrolyte containing GNF (0.005 g) can be possibly attributed to the direct contact between dye/TiO{sub 2} and I{sup −}/I{sub 3}{sup −} that will improve the charge transportation. The highest energy conversion efficiency of 4.60% is obtained for polymer electrolyte containing GNF (0.005 g)

  9. Gel-based composite polymer electrolytes with novel hierarchical mesoporous silica network for lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wang Xiaoliang; Cai Qiang [Department of Materials Science and Engineering, and State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University, Beijing 100084 (China); Fan Lizhen [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Hua Tao; Lin Yuanhua [Department of Materials Science and Engineering, and State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University, Beijing 100084 (China); Nan Cewen [Department of Materials Science and Engineering, and State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University, Beijing 100084 (China)], E-mail: cwnan@tsinghua.edu.cn

    2008-11-15

    In the present work, novel gel-based composite polymer electrolytes for lithium batteries were prepared by introducing a hierarchical mesoporous silica network to the poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP)-based gel electrolytes. As compared with the PVDF-HFP-based gel electrolytes with/without conventional nano-sized silica fillers, the novel electrolytes have shown more homogeneous microstructure, higher ionic conductivity and better mechanical stability, which could be caused by the strong silica network and the effective interactions among the polymer, the liquid electrolytes and the silica. Moreover, the cell with this kind of electrolytes could achieve a discharge capacity as much as 150 mAh g{sup -1} at room temperature (LiCoO{sub 2} as the cathode active material), with high Coulomb efficiency.

  10. Gel-based composite polymer electrolytes with novel hierarchical mesoporous silica network for lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xiao-Liang; Cai, Qiang; Hua, Tao; Lin, Yuan-Hua; Nan, Ce-Wen [Department of Materials Science and Engineering, and State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University, Beijing 100084 (China); Fan, Li-Zhen [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China)

    2008-11-15

    In the present work, novel gel-based composite polymer electrolytes for lithium batteries were prepared by introducing a hierarchical mesoporous silica network to the poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP)-based gel electrolytes. As compared with the PVDF-HFP-based gel electrolytes with/without conventional nano-sized silica fillers, the novel electrolytes have shown more homogeneous microstructure, higher ionic conductivity and better mechanical stability, which could be caused by the strong silica network and the effective interactions among the polymer, the liquid electrolytes and the silica. Moreover, the cell with this kind of electrolytes could achieve a discharge capacity as much as 150 mAh g{sup -1} at room temperature (LiCoO{sub 2} as the cathode active material), with high Coulomb efficiency. (author)

  11. 不同分子筛对PVDF-HFP基凝胶态聚合物电解质性能影响%Effect of molecular sieves on the performances of PVDF-HFP-based gel polymer electrolytes

    Institute of Scientific and Technical Information of China (English)

    缪畅; 肖围

    2013-01-01

    通过倒相法制备三种不同分子筛(SAPO-11、MCM-41和ZSM-5)掺杂的PVDF-HFP基复合聚合物电解质膜,将它们分别浸泡于1.0 mol/L LiPF6-EC/DMC/EMC(体积比1∶1∶1)的电解液中活化30 min,得到分子筛改性复合聚合物电解质,并采用SEM、FT-IR、TG-DSC和电化学等手段对其形貌和电化学性能进行表征.SEM结果表明分子筛改性膜表面均匀、孔径适当且内部含有丰富的相互连通的微孔;FT-IR分析结果证明分子筛和聚合物分子间存在某种作用力;TG-DSC结果表明分子筛改性膜的热分解温度有明显的提高,在350℃内能保持很好的热稳定性;EIS和LSV结果表明分子筛改性膜的电导率和电化学稳定窗口得到明显的改进,其中ZSM-5改性膜的电导率和电化学稳定窗口分别高达3.65 mS· cm-1和5.2V.

  12. Porous polymers: enabling solutions for energy applications.

    Science.gov (United States)

    Thomas, Arne; Kuhn, Pierre; Weber, Jens; Titirici, Maria-Magdalena; Antonietti, Markus

    2009-02-18

    A new generation of porous polymers was made for various energy-related applications, e.g., as fuel cell membranes, as electrode materials for batteries, for gas storage, partly from renewable resources. This review intends to catch this emerging field by reporting on a variety of different approaches to make high performing polymers porous. This includes template techniques, polymers with inherent microporosity, polymer frameworks by ionothermal polymerization, and the polymerization of carbon from appropriate precursors and by hydrothermal polymerization. In this process, we try to not only identify the current status of the field, but also point to open question and tasks to identify the potentially relevant progress.

  13. Functional porous organic polymers for heterogeneous catalysis.

    Science.gov (United States)

    Zhang, Yugen; Riduan, Siti Nurhanna

    2012-03-21

    Porous organic polymers (POPs), a class of highly crosslinked amorphous polymers possessing nano-pores, have recently emerged as a versatile platform for the deployment of catalysts. The bottom-up approach for porous organic polymer synthesis provides the opportunity for the design of polymer frameworks with various functionalities, for their use as catalysts or ligands. This tutorial review focuses on the framework structures and functionalities of catalytic POPs. Their structural design, functional framework synthesis and catalytic reactions are discussed along with some of the challenges.

  14. Adsorption Kinetics in Nanoscale Porous Coordination Polymers

    Energy Technology Data Exchange (ETDEWEB)

    Nune, Satish K.; Thallapally, Praveen K.; McGrail, Benard Peter; Annapureddy, Harsha V. R.; Dang, Liem X.; Mei, Donghai; Karri, Naveen; Alvine, Kyle J.; Olszta, Matthew J.; Arey, Bruce W.; Dohnalkova, Alice

    2015-10-07

    Nanoscale porous coordination polymers were synthesized using simple wet chemical method. The effect of various polymer surfactants on colloidal stability and shape selectivity was investigated. Our results suggest that the nanoparticles exhibited significantly improved adsorption kinetics compared to bulk crystals due to decreased diffusion path lengths and preferred crystal plane interaction.

  15. Porous polymers based on aryleneethynylene building blocks.

    Science.gov (United States)

    Bunz, Uwe H F; Seehafer, Kai; Geyer, Florian L; Bender, Markus; Braun, Ingo; Smarsly, Emanuel; Freudenberg, Jan

    2014-09-01

    Porous conjugated polymers are synthesized by metal-catalyzed coupling reactions. The progress for porous polymers when planar or tetrahedral building blocks are connected by alkyne units into novel materials is highlighted. The most prominent reaction for the buildup of the microporous alkyne-bridged polymers is the Sonogashira reaction, connecting alkynes to aromatic iodides or bromides. The availability of the building blocks and the potency of the Sonogashira reaction allow preparing a large variety of intrinsically porous polymeric materials, in which rigid struts connect multipronged centers. The microporous polymers are used as catalysts and as storage materials for gases and sensors. Postfunctionalization schemes, understanding of structure-property relationships, and the quest for high porosity are pertinent.

  16. Impregnation of porous silicon with conducting polymers

    Energy Technology Data Exchange (ETDEWEB)

    Harraz, Farid A. [Advanced Materials Technology Department, Central Metallurgical Research and Development Institute (CMRDI), PO Box: 87, Hewan, 11421 Cairo (Egypt)

    2011-06-15

    Fabrication of porous silicon layers using the electrochemical technique followed by filling the nanopores with a group of conducting polymers is investigated. Our findings revealed that the deposition of polymer proceeds homogeneously inside the nanopores strating from the pore bottom and propagates into the outer surface. The polymerization process was conducted and controlled by the potentiostatic and galvanostatic modes with characteristic, defined polymerization stages. As-formed hybrid nanocomposites were characterized using different analytical techniques. Polypyrrole, polyaniline and polythiophene were tested in this study. By selective dissolution of porous silicon template, polymeric nanowires were obtained. The fabrication process, the electrochemical measurements and the porous silicon filling mechanism with polymer are thoroughly addressed and discussed (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  17. Microfluidic devices and methods including porous polymer monoliths

    Science.gov (United States)

    Hatch, Anson V; Sommer, Gregory J; Singh, Anup K; Wang, Ying-Chih; Abhyankar, Vinay V

    2014-04-22

    Microfluidic devices and methods including porous polymer monoliths are described. Polymerization techniques may be used to generate porous polymer monoliths having pores defined by a liquid component of a fluid mixture. The fluid mixture may contain iniferters and the resulting porous polymer monolith may include surfaces terminated with iniferter species. Capture molecules may then be grafted to the monolith pores.

  18. Porous Organic Polymers for CO2 Capture

    KAUST Repository

    Teng, Baiyang

    2013-05-01

    Carbon dioxide (CO2) has long been regarded as the major greenhouse gas, which leads to numerous negative effects on global environment. The capture and separation of CO2 by selective adsorption using porous materials proves to be an effective way to reduce the emission of CO2 to atmosphere. Porous organic polymers (POPs) are promising candidates for this application due to their readily tunable textual properties and surface functionalities. The objective of this thesis work is to develop new POPs with high CO2 adsorption capacities and CO2/N2 selectivities for post-combustion effluent (e.g. flue gas) treatment. We will also exploit the correlation between the CO2 capture performance of POPs and their textual properties/functionalities. Chapters Two focuses on the study of a group of porous phenolic-aldehyde polymers (PPAPs) synthesized by a catalyst-free method, the CO2 capture capacities of these PPAPs exceed 2.0 mmol/g at 298 K and 1 bar, while keeping CO2/N2 selectivity of more than 30 at the same time. Chapter Three reports the gas adsorption results of different hyper-cross-linked polymers (HCPs), which indicate that heterocyclo aromatic monomers can greatly enhance polymers’ CO2/N2 selectivities, and the N-H bond is proved to the active CO2 adsorption center in the N-contained (e.g. pyrrole) HCPs, which possess the highest selectivities of more than 40 at 273 K when compared with other HCPs. Chapter Four emphasizes on the chemical modification of a new designed polymer of intrinsic microporosity (PIM) with high CO2/N2 selectivity (50 at 273 K), whose experimental repeatability and chemical stability prove excellent. In Chapter Five, we demonstrate an improvement of both CO2 capture capacity and CO2/N2 selectivity by doping alkali metal ions into azo-polymers, which leads a promising method to the design of new porous organic polymers.

  19. Porous Polyolefin Films via Polymer Blends

    Science.gov (United States)

    Macosko, Chris

    Porous polymer films have broad application including battery separators, membrane supports and filters. Polyolefins are attractive for these applications because of their solvent resistance, low electrical and thermal conductivity, easy fabrication and cost. We will describe fabrication of porous films using cocontinuous blends of a polyolefin with another polymer which can be readily removed with a solvent. Methods to image and control the cocontinuous morphology will be presented.Bell, J. R., K. Chang, C. R. Lopez-Barron, C. W. Macosko, and D. C. Morse, ''Annealing of cocontinuous polymer blends: effect of block copolymer molecular weight and architecture,'' Macromolecules 43, 5024-5032 (2010).Lopez-Barron, C. R., and C. W. Macosko, ''Direct measurement of interface anisotropy of bicontinuous structures via 3D image analysis,'' Langmuir 26, 14284-14293 (2010).Trifkovic, M., A. T. Hedegaard, K. Huston, M. Sheikhzadeh, and C. W. Macosko, ''Porous films via PE/PEO cocontinuous blends,'' Macromolecules 45, 6036-6044 (2012).Hedegaard, A.T., L.L. Gu and C. W. Macosko, ``Effect of Extensional Viscosity on Cocontinuity of Immiscible Polymer Blends'' J. Rheol. 59, 1397-1417 (2015).

  20. Cationic polymers and porous materials

    KAUST Repository

    Han, Yu

    2017-04-27

    According to one or more embodiments, cationic polymers may be produced which include one or more monomers containing cations. Such cationic polymers may be utilized as structure directing agents to form mesoporous zeolites. The mesoporous zeolites may include micropores as well as mesopores, and may have a surface area of greater than 350 m2/g and a pore volume of greater than 0.3 cm3/g. Also described are core/shell zeolites, where at least the shell portion includes a mesoporous zeolite material.

  1. Distributed Pore Chemistry in Porous Organic Polymers

    Science.gov (United States)

    Koontz, Steven L. (Inventor)

    1999-01-01

    A method for making a biocompatible polymer article using a uniform atomic oxygen treatment is disclosed. The substrate may be subsequently optionally grated with a compatibilizing compound. Compatibilizing compounds may include proteins, phosphorylcholine groups, platelet adhesion preventing polymers, albumin adhesion promoters, and the like. The compatibilized substrate may also have a living cell layer adhered thereto. The atomic oxygen is preferably produced by a flowing afterglow microwave discharge. wherein the substrate resides in a sidearm out of the plasma. Also, methods for culturing cells for various purposes using the various membranes are disclosed as well. Also disclosed are porous organic polymers having a distributed pore chemistry (DPC) comprising hydrophilic and hydrophobic regions. and a method for making the DPC by exposing the polymer to atomic oxygen wherein the rate of hydrophilization is greater than the rate of mass loss.

  2. Electrocatalysts using porous polymers and method of preparation

    Science.gov (United States)

    Liu, Di-Jia; Yuan, Shengwen; Goenaga, Gabriel A.

    2016-08-02

    A method of producing an electrocatalyst article using porous polymers. The method creates a porous polymer designed to receive transition metal groups disposed at ligation sites and activating the transition metals to form an electrocatalyst which can be used in a fuel cell. Electrocatalysts prepared by this method are also provided. A fuel cell which includes the electrocatalyst is also provided.

  3. Recent Advances in Boron-Containing Conjugated Porous Polymers

    Directory of Open Access Journals (Sweden)

    Feng Qiu

    2016-05-01

    Full Text Available Porous polymers, integrating the advantages of porous materials and conventional polymers, have been well developed and exhibited tremendous attention in the fields of material, chemistry and biology. Of these, boron-containing conjugated porous polymers, featuring tunable geometric structures, unique Lewis acid boron centers and very rich physical properties, such as high specific surface, chargeable scaffold, strong photoluminescence and intramolecular charge transfer, have emerged as one of the most promising functional materials for optoelectronics, catalysis and sensing, etc. Furthermore, upon thermal treatment, some of them can be effectively converted to boron-doped porous carbon materials with good electrochemical performance in energy storage and conversion, extensively enlarging the applicable scope of such kinds of polymers. In this review, the synthetic approaches, structure analyses and various applications of the boron-containing conjugated porous polymers reported very recently are summarized.

  4. Photoinitiated grafting of porous polymer monoliths and thermoplastic polymers for microfluidic devices

    Science.gov (United States)

    Frechet, Jean M. J.; Svec, Frantisek; Rohr, Thomas

    2008-10-07

    A microfluidic device preferably made of a thermoplastic polymer that includes a channel or a multiplicity of channels whose surfaces are modified by photografting. The device further includes a porous polymer monolith prepared via UV initiated polymerization within the channel, and functionalization of the pore surface of the monolith using photografting. Processes for making such surface modifications of thermoplastic polymers and porous polymer monoliths are set forth.

  5. From Plastic to Silicone: The Novelties in Porous Polymer Fabrications

    Directory of Open Access Journals (Sweden)

    Soumaya Berro

    2015-01-01

    Full Text Available Porous polymers are gaining increased interest in several areas due, in great part, to their large surface area and unique physiochemical properties. Porous polymers are conventionally manufactured using specific processes related to the chemical structure of each polymer. With the wide variety of porous polymers that have been designed, fabricated, and tested to date, this review aims to provide an overview of the advances and recent progress in the preparation processes and fabrication techniques. A detailed comparison between these techniques is also provided. Some of these techniques offer the advantage of controlling the porosity and the possibility to obtain porous 3D polymers. A new generic fabrication process that can be applied to all liquid polymers to texture their outer surfaces with a desired porosity is also presented. The proposed process, which is based on two micromolding steps, offers flexibility in terms of tailoring the texture of the final polymer by simply using porous silicon templates with different pore sizes and configurations. The anticipated process was successfully implemented to texture polyethyl hydrosiloxane (PMHS using porous silicon and polymethyl methacrylate (PMMA scaffolds.

  6. Soft porous crystal meets TCNQ: charge transfer-type porous coordination polymers

    OpenAIRE

    Shimomura, Satoru; Kitagawa, Susumu

    2011-01-01

    The significant progress of porous coordination polymers (or metal–organic frameworks) has been attracting the attention of a lot of scientists in various disciplines and encouraging their entry into this field. The synergy of diverse scientific senses brings further spread of the chemistry of porous coordination polymers. In this review, we introduced the recent developments in PCPs resulting from the hybridization with TCNQ chemistry. Electronic and structural diversities of TCNQ provide no...

  7. Conductive Polymer Porous Film with Tunable Wettability and Adhesion

    Directory of Open Access Journals (Sweden)

    Yuqi Teng

    2015-04-01

    Full Text Available A conductive polymer porous film with tunable wettability and adhesion was fabricated by the chloroform solution of poly(3-hexylthiophene (P3HT and [6,6]-phenyl-C61-butyricacid-methyl-ester (PCBM via the freeze drying method. The porous film could be obtained from the solution of 0.8 wt%, whose pore diameters ranged from 50 nm to 500 nm. The hydrophobic porous surface with a water contact angle (CA of 144.7° could be transferred into a hydrophilic surface with CA of 25° by applying a voltage. The water adhesive force on the porous film increased with the increase of the external voltage. The electro-controllable wettability and adhesion of the porous film have potential application in manipulating liquid collection and transportation.

  8. Porous polymer networks and ion-exchange media and metal-polymer composites made therefrom

    Energy Technology Data Exchange (ETDEWEB)

    Kanatzidis, Mercouri G.; Katsoulidis, Alexandros

    2016-10-18

    Porous polymeric networks and composite materials comprising metal nanoparticles distributed in the polymeric networks are provided. Also provided are methods for using the polymeric networks and the composite materials in liquid- and vapor-phase waste remediation applications. The porous polymeric networks, are highly porous, three-dimensional structures characterized by high surface areas. The polymeric networks comprise polymers polymerized from aldehydes and phenolic molecules.

  9. Flow of polymer fluids through porous media

    OpenAIRE

    Zami-Pierre, Frédéric; Davit, Yohan; Loubens, Romain de; Quintard, Michel

    2016-01-01

    Non-Newtonian fluids are extensively used in enhanced oil recovery. However, understanding the flow of such fluids in complex porous media remains a challenging problem. In the presented study, we use computational fluid dynamics to investigate the creeping flow of a particular non-Newtonian fluid through porous media, namely a power-law fluid with a newtonian behavior below a critical shear rate. We show that the nonlinear effects induced by the rheology only weakly impact the topological st...

  10. Method for dialysis on microchips using thin porous polymer membrane

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Anup K. (San Francisco, CA); Kirby, Brian J. (San Francisco, CA); Shepodd, Timothy J. (Livermore, CA)

    2009-05-19

    Laser-induced phase-separation polymerization of a porous acrylate polymer is used for in-situ fabrication of dialysis membranes inside glass microchannels. A shaped 355 nm laser beam is used to produce a porous polymer membrane with a thickness of about 15 .mu.m, which bonds to the glass microchannel and forms a semi-permeable membrane. Differential permeation through a membrane formed with pentaerythritol triacrylate was observed and quantified by comparing the response of the membrane to fluorescein and fluorescently tagging 200 nm latex microspheres. Differential permeation was observed and quantified by comparing the response to rhodamine 560 and lactalbumin protein in a membrane formed with SPE-methylene bisacrylamide. The porous membranes illustrate the capability for the present technique to integrate sample cleanup into chip-based analysis systems.

  11. Dialysis on microchips using thin porous polymer membranes

    Science.gov (United States)

    Singh, Anup K.; Kirby, Brian J.; Shepodd, Timothy J.

    2007-09-04

    Laser-induced phase-separation polymerization of a porous acrylate polymer is used for in-situ fabrication of dialysis membranes inside glass microchannels. A shaped 355 nm laser beam is used to produce a porous polymer membrane with a thickness of about 15 .mu.m, which bonds to the glass microchannel and form a semi-permeable membrane. Differential permeation through a membrane formed with pentaerythritol triacrylate was observed and quantified by comparing the response of the membrane to fluorescein and fluorescently tagging 200 nm latex microspheres. Differential permeation was observed and quantified by comparing the response to rhodamine 560 and lactalbumin protein in a membrane formed with SPE-methylene bisacrylamide. The porous membranes illustrate the capability for the present technique to integrate sample cleanup into chip-based analysis systems.

  12. Flow of polymer solutions through porous media

    OpenAIRE

    Denys, K.F.J.

    2003-01-01

    These days leading oil and gas producing companies are investing increasing amounts of money into the development of non-fossil energy sources like wind-, solar-, biomass energy and forestry. On the other hand these companies are persisting in developing techniques to make energy recovery more efficient intending to stretch the life span of fossil resources. One of the more mature techniques to improve recovery efficiency is polymer flooding. Herein polymer solutions are injected in injector ...

  13. Cell-Culture Reactor Having a Porous Organic Polymer Membrane

    Science.gov (United States)

    Koontz, Steven L. (Inventor)

    2000-01-01

    A method for making a biocompatible polymer article using a uniform atomic oxygen treatment is disclosed. The substrate may be subsequently optionally grated with a compatibilizing compound. Compatibilizing compounds may include proteins, phosphory1choline groups, platelet adhesion preventing polymers, albumin adhesion promoters, and the like. The compatibilized substrate may also have a living cell layer adhered thereto. The atomic oxygen is preferably produced by a flowing afterglow microwave discharge, wherein the substrate resides in a sidearm out of the plasma. Also, methods for culturing cells for various purposes using the various membranes are disclosed as well. Also disclosed are porous organic polymers having a distributed pore chemistry (DPC) comprising hydrophilic and hydrophobic regions, and a method for making the DPC by exposing the polymer to atomic oxygen wherein the rate of hydrophilization is greater than the rate of mass loss.

  14. POROUS MEMBRANE TEMPLATED SYNTHESIS OF POLYMER PILLARED LAYER

    Institute of Scientific and Technical Information of China (English)

    Zhong-wei Niu; Dan Li; Zhen-zhong Yang

    2003-01-01

    The anodic porous alumina membranes with a definite pore diameter and aspect ratio were used as templates to synthesize polymer pillared layer structures. The pillared polymer was produced in the template membrane pores, and the layer on the template surfaces. Rigid cured epoxy resin, polystyrene and soft hydrogel were chosen to confirm the methodology. The pillars were in the form of either tubes or fibers, which were controlled by the alumina membrane pore surface wettability. The structural features were confirmed by scanning electron microscopy results.

  15. MECHANISM FOR VISCOELASTIC POLYMER SOLUTION PERCOLATING THROUGH POROUS MEDIA

    Institute of Scientific and Technical Information of China (English)

    ZHANG Li-juan; YUE Xiang-an

    2007-01-01

    The pore throat of porous media is modeled as a constricted channel or expanded channel. The flow of viscoelastic polymer solution in pore throat model is studied by numerical method. Relationship between pressure drop and flow rate is developed, viscoelasticity and throat size are found to be two main factors in high flow resistance. According to pore throat model, 2-D stochastic channel bundle is put forward to model porous media, which is composed of pore throat models in series - parallel connection with size and length accord to Haring - Greenkorn stochastic distribution. Percolation model of viscoelastic fluid is developed on the basis of Darcy equation and pressure drop vs. flow rate relation in 2-D stochastic channel bundle. Results indicate that the seepage ability of viscoelastic polymer solution decreases with the increase of viscoelasticity, injection rate, and heterogeneity as well as the decrease of mean pore size of porous media. The high pressure drop of viscoelastic fluid at the connection of pore to throat plays a great role in its anomalous high flow resistance through porous media.

  16. 21 CFR 888.3565 - Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Knee joint patellofemorotibial metal/polymer... Devices § 888.3565 Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis is a...

  17. Determination of the effective refractive index of porous silicon/polymer composite films

    Institute of Scientific and Technical Information of China (English)

    Zhenhong Jia

    2005-01-01

    The equation for calculating the effective refractive index of porous silicon inserted polymer was obtained by three-component Bruggeman effective medium model. The dependence of the effective refractive index of porous silicon/polymer composite films on the polymer fraction with various initial porosity was given theorically and experimentally respectively. The porous silicon and polymer polymethylmetacrylate based dispersive red one (PMMA/DR1) composite films were fabricated in our experiments. It is found that the measured effective refractive index of porous silicon inserted polymer was slightly lower than the calculated result because of the oxidization of porous silicon. The effective refractive index of oxidized porous silicon inserted polymer also was analyzed by four-component medium system.

  18. Physicochemical properties of a novel composite polymer electrolyte doped with vinyltrimethoxylsilane-modified nano-La2O3

    Institute of Scientific and Technical Information of China (English)

    XIAO Wei; LI Xinhai; WANG Zhixing; GUO Huajun; WANG Jiexi; HUANG Silin; GAN Lei

    2012-01-01

    Nano-La2O3 was modified with the vinyltrimethoxylsilane by hydrolysis and a novel poly (vinylidene fluoride-co-hexafluoropropylene)(PVDF-HFP) based composite polymer electrolyte doped with the modified nano-La2O3 was prepared by phase inversion method.The physicochemical properties were studied by SEM,FT-IR,XRD,TG and electrochemical methods.The results of FT-IR indicated that the nanoLa2O3 was successfully modified with vinyltrimethoxylsilane.The XRD analysis showed that the incorporation of modified nano-La2O3 into the polymer electrolyte membranes could effectively reduce the crystallinity of PVDF-HFP,and the characterizations also suggested that thermal stability and electrochemical stability window could reach to 382 ℃ and 5.1 V,respectively; the reciprocal temperature dependence of ionic conductivity followed Vogel-Tamman-Fulcher (VTF) relation,ionic conductivity at room temperature was up to 3.5× 10-3 S/cm and lithium ions transference number was up to 0.42; the interfacial resistance increased at initial value about 353 Ω/cm2 and reached a steady value about 559 Ω/cm2 after 5 d storage at 30 ℃.The fabricated Li/As-prepared electrolytes/LiCoO2 coin cell showed excellent rate and cycle performances.

  19. Static Corrosion Test of Porous Iron Material with Polymer Coating

    Science.gov (United States)

    Markušová-Bučková, Lucia; Oriňaková, Renáta; Oriňak, Andrej; Gorejová, Radka; Kupková, Miriam; Hrubovčáková, Monika; Baláž, Matej; Kováľ, Karol

    2016-12-01

    At present biodegradable implants received increased attention due to their use in various fields of medicine. This work is dedicated to testing of biodegradable materials which could be used as bone implants. The samples were prepared from the carbonyl iron powder by replication method and surface polymer film was produced through sol-gel process. Corrosion testing was carried out under static conditions during 12 weeks in Hank's solution. The quantity of corrosion products increased with prolonging time of static test as it can be concluded from the results of EDX analysis. The degradation of open cell materials with polyethylene glycol coating layer was faster compared to uncoated Fe sample. Also the mass losses were higher for samples with PEG coating. The polymer coating brought about the desired increase in degradation rate of porous iron material.

  20. Design, preparation, and application of ordered porous polymer materials

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Qingquan, E-mail: qqliu@hnust.edu.cn; Tang, Zhe; Ou, Baoli; Liu, Lihua; Zhou, Zhihua, E-mail: zhou7381@126.com; Shen, Shaohua; Duan, Yinxiang

    2014-04-01

    Ordered porous polymer (OPP) materials have extensively application prospects in the field of separation and purification, biomembrane, solid supports for sensors catalysts, scaffolds for tissue engineering, photonic band gap materials owing to ordered pore arrays, uniform and tunable pore size, high specific surface area, great adsorption capacity, and light weight. The present paper reviewed the preparation techniques of OPP materials like breath figures, hard template, and soft template. Finally, the applications of OPP materials in the field of separation, sensors, and biomedicine are introduced, respectively. - Highlights: • Breath figures involve polymer casting under moist ambience. • Hard template employs monodisperse colloidal spheres as a template. • Soft template utilizes the etched block in copolymers as template.

  1. Interpenetration in coordination polymers: structural diversities toward porous functional materials

    Directory of Open Access Journals (Sweden)

    Ritesh Haldar

    2015-03-01

    Full Text Available Interpenetration is a natural phenomenon frequently encountered in porous coordination polymers (PCPs or metal-organic frameworks (MOFs. Traditionally interpenetration has been considered as a threat to permanent porosity and several strategies have been adopted to control the framework interpenetration. Recent literature reports have unveiled that interpenetration has paramount importance in several material properties particularly in storage and separation of small gas molecules. Such frameworks also show interesting structural flexibility based on shearing or movement of the nets and also reveals guest induced dynamic structural transformation for modulated specific functions. In this review, we will emphasize several interpenetration phenomena observed in coordination polymers, their intriguing structural aspects and fascinating material properties.

  2. Porous-Hybrid Polymers as Platforms for Heterogeneous Photochemical Catalysis

    KAUST Repository

    Haikal, Rana R.

    2016-07-18

    A number of permanently porous polymers containing Ru(bpy)n photosensitizer or a cobaloxime complex, as a proton-reduction catalyst, were constructed via one-pot Sonogashira-Hagihara (SH) cross-coupling reactions. This process required minimal workup to access porous platforms with control over the apparent surface area, pore volume, and chemical functionality from suitable molecular building blocks (MBBs) containing the Ru or Co complexes, as rigid and multi-topic nodes. The cobaloxime molecular building block, generated through in situ metalation, afforded a microporous solid that demonstrated noticeable catalytic activity towards hydrogen-evolution reaction (HER) with remarkable recyclability. We further demonstrated, in two cases, the ability to affect the excited state lifetime of the covalently-immobilized Ru(bpy)3 complex attained through deliberate utilization of the organic linkers of variable dimensions. Overall, this approach facilitates construction of tunable porous solids, with hybrid composition and pronounced chemical and physical stability, based on the well-known Ru(bpy)nor the cobaloxime complexes.

  3. Porous polymer electrolytes with high ionic conductivity and good mechanical property for rechargeable batteries

    Science.gov (United States)

    Liang, Bo; Jiang, Qingbai; Tang, Siqi; Li, Shengliang; Chen, Xu

    2016-03-01

    Porous polymer electrolytes (PPEs) are attractive for developing lithium-ion batteries because of the combined advantages of liquid and solid polymer electrolytes. In the present study, a new porous polymer membrane doped with phytic acid (PA) is prepared, which is used as a crosslinker in polymer electrolyte matrix and can also plasticize porous polymer electrolyte membranes, changing them into soft tough flexible materials. A PEO-PMMA-LiClO4-x wt.% PA (x = weight of PA/weight of polymer, PEO: poly(ethylene oxide); PMMA: poly(methyl methacrylate)) polymer membrane is prepared by a simple evaporation method. The effects of the ratio of PA to PEO-PMMA on the properties of the porous membrane, including morphology, porous structure, and mechanical property, are systematically studied. PA improves the porous structure and mechanical properties of polymer membrane. The maximum tensile strength and elongation of the porous polymer membranes are 20.71 MPa and 45.7% at 15 wt.% PA, respectively. Moreover, the PPEs with 15 wt.% PA has a conductivity of 1.59 × 10-5 S/cm at 20 °C, a good electrochemical window (>5 V), and a low interfacial resistance. The results demonstrate the compatibility of the mechanical properties and conductivity of the PPEs, indicating that PPEs have good application prospects for lithium-ion batteries.

  4. Click-based porous cationic polymers for enhanced carbon dioxide capture

    OpenAIRE

    Dani, Alessandro; Magistris, Valentina Crocella Claudio; Santoro, Valentina; Yuan, Jiayin; Bordiga, Silvia

    2017-01-01

    Imidazolium based porous cationic polymers were synthesized using an innovative and facile approach, which takes advantage of the Debus Radziszewski reaction to obtain meso- and microporous polymers following click chemistry principles. In the obtained set of materials, click based porous cationic polymers have the same cationic backbone, whereas they bear the commonly used anions of imidazolium poly(ionic liquid)s. These materials show hierarchical porosity and a good specific surface area. ...

  5. Oriented immobilization of proteins on grafted porous polymers

    Energy Technology Data Exchange (ETDEWEB)

    Carbajal, M. Laura; Smolko, Eduardo E.; Grasselli, Mariano E-mail: mgrasse@unq.edu.ar

    2003-08-01

    The modification of polymers by radiation grafting has been utilized for several decades. The penetrability of gamma rays allows to modify the internal surfaces of porous materials retaining its mechanical properties. In recent years applications of these materials to obtain chromatographic supports and biocatalysts have been reported. In this work, we described the grafting of glycidyl methacrylate (GMA) onto a macroporous polysulfone polymer. Reproducible amount of grafting, from 10% to 60% was obtained by choosing favourable monomer concentration and gamma radiation doses from 6 kGy up. Afterwards, iminodiacetic acid (IDA) and amino phenyl arsine oxide (PAO) were covalently attached to the grafted polyGMA, in correspondence with the grafting degree. Later on, a recombinant histidin-patch thioredoxin protein (HP-rTrx) was immobilized onto this surface by two different ways, involving specific protein orientations. The first one involves an IDA-Ni{sup 2+} complex and three HP-rTrx's histidines and the other one involves a co-ordination site between PAO and two proximal HP-rTrx's cysteines, which corresponds to the active site of the enzyme. Specific polyclonal antibodies recognize HP-rTrx on the polymer. Proper orientation of the protein was confirmed by HP-rTrx activity measurements. The described procedure allows the successful oriented immobilization of a protein onto a macroporous polysulfone material.

  6. Enhanced photoluminescence of porous silicon nanoparticles coated by bioresorbable polymers

    Science.gov (United States)

    Gongalsky, Maxim B.; Kharin, Alexander Yu; Osminkina, Liubov A.; Timoshenko, Victor Yu; Jeong, Jinyoung; Lee, Han; Chung, Bong Hyun

    2012-08-01

    A significant enhancement of the photoluminescence (PL) efficiency is observed for aqueous suspensions of porous silicon nanoparticles (PSiNPs) coated by bioresorbable polymers, i.e., polylactic-co-glycolic acid (PLGA) and polyvinyl alcohol (PVA). PSiNPs with average size about 100 nm prepared by mechanical grinding of electrochemically etched porous silicon were dispersed in water to prepare the stable suspension. The inner hydrophobic PLGA layer prevents the PSiNPs from the dissolution in water, while the outer PVA layer makes the PSiNPs hydrophilic. The PL quantum yield of PLGA/PVA-coated PSiNPs was found to increase by three times for 2 weeks of the storage in water. The observed effect is explained by taking into account both suppression of the dissolution of PSiNPs in water and a process of the passivation of nonradiative defects in PSiNPs. The obtained results are interesting in view of the potential applications of PSiNPs in bioimaging.

  7. Porous Organic Polymers for Post-Combustion Carbon Capture.

    Science.gov (United States)

    Zou, Lanfang; Sun, Yujia; Che, Sai; Yang, Xinyu; Wang, Xuan; Bosch, Mathieu; Wang, Qi; Li, Hao; Smith, Mallory; Yuan, Shuai; Perry, Zachary; Zhou, Hong-Cai

    2017-10-01

    One of the most pressing environmental concerns of our age is the escalating level of atmospheric CO2 . Intensive efforts have been made to investigate advanced porous materials, especially porous organic polymers (POPs), as one type of the most promising candidates for carbon capture due to their extremely high porosity, structural diversity, and physicochemical stability. This review provides a critical and in-depth analysis of recent POP research as it pertains to carbon capture. The definitions and terminologies commonly used to evaluate the performance of POPs for carbon capture, including CO2 capacity, enthalpy, selectivity, and regeneration strategies, are summarized. A detailed correlation study between the structural and chemical features of POPs and their adsorption capacities is discussed, mainly focusing on the physical interactions and chemical reactions. Finally, a concise outlook for utilizing POPs for carbon capture is discussed, noting areas in which further work is needed to develop the next-generation POPs for practical applications. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  8. 21 CFR 888.3358 - Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis.

    Science.gov (United States)

    2010-04-01

    ... porous-coated uncemented prosthesis. 888.3358 Section 888.3358 Food and Drugs FOOD AND DRUG... Devices § 888.3358 Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis. (a) Identification. A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a...

  9. Phosphonium salt incorporated hypercrosslinked porous polymers for CO2 capture and conversion.

    Science.gov (United States)

    Wang, Jinquan; Wei Yang, Jason Gan; Yi, Guangshun; Zhang, Yugen

    2015-11-01

    Various novel hypercrosslinked porous polymers with phosphonium salt incorporated into their networks were developed. These porous materials have high BET surface areas (up to 1168 m(2) g(-1)) and can be used to selectively capture CO2 and efficiently convert CO2 into cyclic carbonates.

  10. Mesoscopic architectures of porous coordination polymers fabricated by pseudomorphic replication.

    Science.gov (United States)

    Reboul, Julien; Furukawa, Shuhei; Horike, Nao; Tsotsalas, Manuel; Hirai, Kenji; Uehara, Hiromitsu; Kondo, Mio; Louvain, Nicolas; Sakata, Osami; Kitagawa, Susumu

    2012-06-24

    The spatial organization of porous coordination polymer (PCP) crystals into higher-order structures is critical for their integration into separation systems, heterogeneous catalysts, ion/electron transport and photonic devices. Here, we demonstrate a rapid method to spatially control the nucleation site, leading to the formation of mesoscopic architecture made of PCPs, in both two and three dimensions. Inspired by geological processes, this method relies on the morphological replacement of a shaped sacrificial metal oxide used both as a metal source and as an 'architecture-directing agent' by an analogous PCP architecture. Spatiotemporal harmonization of the metal oxide dissolution and the PCP crystallization allowed the preservation of very fine mineral morphological details of periodic alumina inverse opal structures. The replication of randomly structured alumina aerogels resulted in a PCP architecture with hierarchical porosity in which the hydrophobic micropores of the PCP and the mesopores/macropores inherited from the parent aerogels synergistically enhanced the material's selectivity and mass transfer for water/ethanol separation.

  11. Alignment mechanism of liquid crystal in a stretched porous polymer film

    Science.gov (United States)

    Fujikake, Hideo; Kuboki, Masashi; Murashige, Takeshi; Sato, Hiroto; Kikuchi, Hiroshi; Kurita, Taiichiro

    2003-09-01

    This article discusses the mechanism of nematic liquid crystal alignment in stretched porous polymer films. The polymer films were formed by extreme stretching of an isotropic porous polyolefin, such that the draw ratio was 12:1. A 6-μm-thick porous film with a high porosity coefficient of 92% revealed fine string-shaped areas that exhibited optical anisotropy due to their possessing a high degree of molecular alignment. The porous film was filled with nematic liquid crystal and then the composite film was sandwiched between transparent electrodes coated onto glass substrates, without the use of conventional alignment layers. From polarizing microscopy observations it was found that the string-like polymer areas induce liquid crystal molecular alignment. The liquid crystal cells can exhibit an electrically controlled birefringence effect. This alignment technique enables us to realize three-dimensional control of liquid crystal alignment.

  12. The electret effect and electromechanical properties of solid and porous polymers

    Science.gov (United States)

    Tai, Liang Shiang

    Electret effect, pseudo-piezoelectricity and electrostriction of solid and porous polymers were investigated in this study where solid polymers include polyethylene terephthalate (PET), polyvinylidenefluoride (PVDF), poly(vinylidenefluoride-trifluoroethylene) P(VDF-TrFE), polytetrafluoroethylene (PTFE) and fluoroethylenepropylene (FEP). Besides porous PTFE, new porous copolymer P(VDF-TrFE) films were also prepared and used in this work. Capacitive probe and high resolution TSDC techniques were employed for the measurement of surface potential and relaxation of thermal current respectively. Quasi-static piezoelectricity (d33) of solid and porous polymers were determined by measuring the change of induced charge density from the samples after a static load was applied in the thickness direction. By using a modified Michelson interferometer capable of resolving displacements of 3 nm, field-induced strains of the corona-charged samples were measured along the direction of the applied electric field. After corona charging, multi-layer polar PET films were inspected and it was found that the characteristics of polarization and space charges of the individual layers were quite similar to each other. Almost identical surface potentials and TSDC responses were observed for single film and multi-layer sample. New porous ferroelectric P(VDF-TrFE) 56/44 and 70/30 films were fabricated successfully by electrospinning method. These porous and highly flexible polymer films consisted of nano-sized fibril connected with micro-sized spheres and the porosity was about 80%. Dielectric analysis revealed that these porous copolymers possessed the relaxor-like ferroelectric properties with low effective dielectric constant (epsilonr ˜ 1.6). The quasi-static piezoelectric coefficients (d 33 ˜ 300 pC/N) of the porous copolymers were comparable to solid and porous PTFE. Pseudo-piezoelectric effects of double and triple layers based on porous copolymer with bulk PET were significantly

  13. Preparation of Porous Biodegradable Polymer and Its Nanocomposites by Supercritical CO2 Foaming for Tissue Engineering

    Directory of Open Access Journals (Sweden)

    Xia Liao

    2012-01-01

    Full Text Available Using supercritical carbon dioxide (scCO2 as an alternative to conventional methods in the preparation of porous biodegradable polymer and polymer/nanocomposites for tissue engineering has attracted increasing interest in recent years due to the absence of using organic solvents and the ability to incorporate thermosensitive biologicals without loss of bioactivity. Additionally, scCO2 can exert a high level of control over porosity and morphology of scaffolds by tuning the processing parameters. This paper describes the newly achievements on the preparation of porous polymer materials using scCO2 foaming technology with focus on the porous biodegradable materials and its nanocomposites relevant to tissue engineering.

  14. A three-dimensional porous scaffold of biodegradable synthetic polymers and porous hydroxyapatite beads for bone tissue engineering

    Energy Technology Data Exchange (ETDEWEB)

    Ushida, T.; Tateishi, T. [Tokyo Univ. (Japan). Tissue Engineering Lab.; National Inst. for Advanced Interdisciplinary Research, Tsukuba (Japan). 3D Tissue Engineering Group; Chen, G. [National Inst. for Advanced Interdisciplinary Research, Tsukuba (Japan). 3D Tissue Engineering Group; Tamaki, T. [Nippon Inst. of Technology, Saitama (Japan). Dept. of Mechanical Engineering; Umezu, Y. [Advance Co., Saitama (Japan)

    2001-07-01

    A three-dimensional porous scaffold for bone tissue engineering was prepared by hybridizing biodegradable poly(DL-lactic-co-glycolic acid) (PLGA) with porous hydroxyapatite (HAp) beads. At first, porous HAp beads were prepared by dropping the calcium hydrophosphates slurry into liquid nitrogen, freeze-drying and sintering. Observation of the porous HAp beads by scanning electron microscopy (SEM) showed that the beads were almost spherical with pores surrounding them. And then PLGA-HAp hybrid sponge was prepared by a particulate-leaching technique using sieved sodium chloride particulates as a porogen material. SEM observation demonstrated that porous HAp beads uniformly distributed in the interconnected PLGA sponge. PLGA polymer maintained the integrity of the hybrid sponge. The porosity of the hybrid relied on the porosity of HAp beads and weight ratio of sodium chloride particulates. An increase of NaCl resulted in high porosity. In vitro experiments showed that the PLGA-HAp hybrid did not prevent the cells, derived from murine bone marrow, from adhering on the hybrid and being differentiated into osteoblast-like cells. (orig.)

  15. Preparation of carbon monoliths having tailored pore structure from porous polymer precursors

    Energy Technology Data Exchange (ETDEWEB)

    Lagasse, R.R.

    1993-04-01

    This work concerns preparing tailored porous carbon monoliths by pyrolyzing porous polymer precursors. Prior work in this laboratory (1) demonstrated that a low density (0.05 g/cm{sup 3}), high void fraction (97 vol%) carbon monolith could be prepared by pyrolyzing a porous poly(acrylonitrile) (PAN) precursor. A higher density, more robust carbon material is preferred for certain applications, such as electrodes for electrochemical devices. The present work demonstrates that porous carbon monoliths having mass density of 0.7 g/cm{sup 3} can be prepared from a porous PAN precursor if the pyrolysis is controlled carefully. The macropore structure of the carbon is adjusted by changing the pore structure of the PAN precursor, and the finer scale structure (such as the crystallite size L{sub c}) is adjusted by varying the pyrolysis or heat treatment temperature.

  16. Preparation of carbon monoliths having tailored pore structure from porous polymer precursors

    Energy Technology Data Exchange (ETDEWEB)

    Lagasse, R.R.

    1993-01-01

    This work concerns preparing tailored porous carbon monoliths by pyrolyzing porous polymer precursors. Prior work in this laboratory (1) demonstrated that a low density (0.05 g/cm[sup 3]), high void fraction (97 vol%) carbon monolith could be prepared by pyrolyzing a porous poly(acrylonitrile) (PAN) precursor. A higher density, more robust carbon material is preferred for certain applications, such as electrodes for electrochemical devices. The present work demonstrates that porous carbon monoliths having mass density of 0.7 g/cm[sup 3] can be prepared from a porous PAN precursor if the pyrolysis is controlled carefully. The macropore structure of the carbon is adjusted by changing the pore structure of the PAN precursor, and the finer scale structure (such as the crystallite size L[sub c]) is adjusted by varying the pyrolysis or heat treatment temperature.

  17. Modelling multiphase flow inside the porous media of a polymer electrolyte membrane fuel cell

    DEFF Research Database (Denmark)

    Berning, Torsten; Kær, Søren Knudsen

    2011-01-01

    Transport processes inside polymer electrolyte membrane fuel cells (PEMFC’s) are highly complex and involve convective and diffusive multiphase, multispecies flow through porous media along with heat and mass transfer and electrochemical reactions in conjunction with water transport through...... an electrolyte membrane. We will present a computational model of a PEMFC with focus on capillary transport of water through the porous layers and phase change and discuss the impact of the liquid phase boundary condition between the porous gas diffusion layer and the flow channels, where water droplets can...

  18. A foaming process to prepare porous polymer membrane for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Li, Z.H. [Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University, Hunan 411105 (China); New Energy and Materials Laboratory (NEML), Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433 (China)], E-mail: lzh69@xtu.edu.cn; Cheng, C.; Zhan, X.Y. [Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University, Hunan 411105 (China); Wu, Y.P. [New Energy and Materials Laboratory (NEML), Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433 (China)], E-mail: wuyp@fudan.edu.cn; Zhou, X.D. [State Key Laboratory of Chemical Engineering, East China University of Science and Technology, Shanghai 200237 (China)

    2009-07-15

    A foaming process was used to prepare porous polymer membranes (PPMs) based on poly(vinylidene diflouride-co-hexafluoropropylene) copolymer for lithium ion batteries. In this simple process, urea, the foaming agent, was decomposed into gases and was removed at an elevated temperature to get the porous structure within the polymer matrix. When the weight ratio of urea to P(VDF-HFP) is 5:6, the PPM presents the highest porosity, 70.2%, and the prepared gelled polymer electrolyte shows an ionic conductivity up to 1.43 x 10{sup -3} S cm{sup -1} at room temperature. This provides another way to prepare gelled polymer electrolytes easily for application in rechargeable lithium batteries.

  19. Gas chromatographic separation of nitrogen, oxygen, argon, and carbon monoxide using custom-made porous polymers from high purity divinylbenzene

    Science.gov (United States)

    Pollock, G. E.; Ohara, D.; Hollis, O. L.

    1984-01-01

    Existing porous polymers were surveyed for their ability to separate the subject gases. Certain products that showed more promise than others were synthesized and the existing synthetic procedures studied and modified to produce new polymers with enhanced ability to separate the subject gases. Evaluation of the porous polymers was carried out practically by gas chromatography at ambient temperature. The modified synthetic procedures were somewhat simpler than the originals. The new porous polymers made with high purity divinylbenzene enabled use of shorter columns to obtain the separations desired.

  20. Solid polymer electrolyte composite membrane comprising laser micromachined porous support

    Science.gov (United States)

    Liu, Han [Waltham, MA; LaConti, Anthony B [Lynnfield, MA; Mittelsteadt, Cortney K [Natick, MA; McCallum, Thomas J [Ashland, MA

    2011-01-11

    A solid polymer electrolyte composite membrane and method of manufacturing the same. According to one embodiment, the composite membrane comprises a rigid, non-electrically-conducting support, the support preferably being a sheet of polyimide having a thickness of about 7.5 to 15 microns. The support has a plurality of cylindrical pores extending perpendicularly between opposing top and bottom surfaces of the support. The pores, which preferably have a diameter of about 5 microns, are made by laser micromachining and preferably are arranged in a defined pattern, for example, with fewer pores located in areas of high membrane stress and more pores located in areas of low membrane stress. The pores are filled with a first solid polymer electrolyte, such as a perfluorosulfonic acid (PFSA) polymer. A second solid polymer electrolyte, which may be the same as or different than the first solid polymer electrolyte, may be deposited over the top and/or bottom of the first solid polymer electrolyte.

  1. Shear Rheology of Suspensions of Porous Zeolite Particles in Concentrated Polymer Solutions

    Science.gov (United States)

    Olanrewaju, Kayode O.; Breedveld, Victor

    2008-07-01

    We present experimental data on the shear rheology of Ultem (polyetherimide)/NMP(l-methyl-2-pyrrolidinone) solutions with and without suspended surface-modified porous/nonporous zeolite (ZSM-5) particles. We found that the porous zeolite suspensions have relative viscosities that significantly exceed the Krieger-Dougherty predictions for hard sphere suspensions. The major origin of this discrepancy is the selective absorption of NMP solvent into the zeolite pores, which raises both the polymer concentration and the particle volume fraction, thus enhancing both the viscosity of the continuous phase Ultem/NMP polymer solution and the particle contribution to the suspension viscosity. Other factors, such as zeolite non-sphericity and specific interactions with Ultem polymer, contribute to the suspension viscosity to a lesser extent. We propose a predictive model for the viscosity of porous zeolite suspensions by incorporating an absorption parameter, α, into the Krieger-Dougherty model. We also propose independent approaches to determine α. The first one is indirect and based on zeolite density/porosity data, assuming that all pores will be filled with solvent. The other method is based on our experimental data, by comparing the viscosity data of porous versus non-porous zeolite suspensions. The different approaches are compared.

  2. Porous polymers for repair and replacement of the knee joint meniscus and articular cartilage

    NARCIS (Netherlands)

    Klompmaker, Jan

    1992-01-01

    The studies presented here were initiated to answer a variety of questions concerning firstly the repair and replacement of the knee joint meniscus and, secondly, the repair of full-thickness defects of articular cartilage. AIMS OF THE STUDIES I To assess the effect of implantation of a porous polym

  3. Characterization of long term field aging of polymer modified bitumen in porous asphalt

    NARCIS (Netherlands)

    Vliet, D. van; Erkens, S.; Leegwater, G.A.

    2012-01-01

    The effect of long term field aging on different types of polymer modified binders used in two-layer porous asphalt is studied using different test methods. Chemical and rheological tests are performed on samples taken from road sections at different moments in time in search of trends in long term

  4. The Development of a High-Throughput/Combinatorial Workflow for the Study of Porous Polymer Networks

    Science.gov (United States)

    2012-04-05

    LM, Chew CH, Teo WK, Gan LH. Preparation of ultrafiltration membranes by direct microemulsion polymerization using polymerizable surfactants ...applications such as tissue scaffolds,1 controlled drug release,2 chromatography,3 separation membranes ,4 piezoelectric materials,5 chemical sensors,6,7...porous polymer materials, CIPS probably provides the greatest versatility with respect to the range of materials that can be generated. In addition , the

  5. Tissue ingrowth polymers and degradation of two biodegradable porous with different porosities and pore sizes

    NARCIS (Netherlands)

    van Tienen, TG; Heijkants, RGJC; Buma, P; de Groot, JH; Pennings, AJ; Veth, RPH

    2002-01-01

    Commonly, spontaneous repair of lesions in the avascular zone of the knee meniscus does not occur. By implanting a porous polymer scaffold in a knee meniscus defect, the lesion is connected with the abundantly vascularized knee capsule and heating can be realized. Ingrowth of fibrovascular tissue an

  6. Tissue ingrowth and degradation of two biodegradable porous polymers with different porosities and pore sizes.

    NARCIS (Netherlands)

    Tienen, Tony van; Heijkants, R.G.J.C.; Buma, P.; Groot, J.H. de; Pennings, A.J.; Veth, R.P.H.

    2002-01-01

    Commonly, spontaneous repair of lesions in the avascular zone of the knee meniscus does not occur. By implanting a porous polymer scaffold in a knee meniscus defect, the lesion is connected with the abundantly vascularized knee capsule and healing can be realized. Ingrowth of fibrovascular tissue an

  7. Modelling multiphase flow inside the porous media of a polymer electrolyte membrane fuel cell

    DEFF Research Database (Denmark)

    Berning, Torsten; Kær, Søren Knudsen

    2011-01-01

    Transport processes inside polymer electrolyte membrane fuel cells (PEMFC’s) are highly complex and involve convective and diffusive multiphase, multispecies flow through porous media along with heat and mass transfer and electrochemical reactions in conjunction with water transport through an el...

  8. Natural Gas Purification Using a Porous Coordination Polymer with Water and Chemical Stability

    NARCIS (Netherlands)

    Duan, J.; Jin, W.; Krishna, R.

    2015-01-01

    Porous coordination polymers (PCPs), constructed by bridging the metals or clusters and organic linkers, can provide a functional pore environment for gas storage and separation. But the rational design for identifying PCPs with high efficiency and low energy cost remains a challenge. Here, we demon

  9. Characterization of long term field aging of polymer modified bitumen in porous asphalt

    NARCIS (Netherlands)

    Vliet, D. van; Erkens, S.; Leegwater, G.A.

    2012-01-01

    The effect of long term field aging on different types of polymer modified binders used in two-layer porous asphalt is studied using different test methods. Chemical and rheological tests are performed on samples taken from road sections at different moments in time in search of trends in long term

  10. Integrated on-chip mass spectrometry reaction monitoring in microfluidic devices containing porous polymer monolithic columns.

    Science.gov (United States)

    Dietze, C; Schulze, S; Ohla, S; Gilmore, K; Seeberger, P H; Belder, D

    2016-09-21

    Chip-based microfluidics enable the seamless integration of different functions into single devices. Here, we present microfluidic chips containing porous polymer monolithic columns as a means to facilitate chemical transformations as well as both downstream chromatographic separation and mass spectrometric analysis. Rapid liquid phase lithography prototyping creates the multifunctional device economically.

  11. Carbon Dioxide Capture from Air Using Amine-Grafted Porous Polymer Networks

    NARCIS (Netherlands)

    Lu, W.; Sculley, J.P.; Yuan, D.; Krishna, R.; Zhou, H.C.

    2013-01-01

    Amine-grafted porous polymer networks were investigated for CO2 capture directly from air (400 ppm CO2, 78.96% N-2, and 21% O-2). Under these ultradilute conditions, PPN-6-CH(2)DETA has an extraordinarily high CO2 selectivity (3.6 x 10(10)) and loading capacity (1.04 mol/kg) as calculated using idea

  12. Carbon Dioxide Capture from Air Using Amine-Grafted Porous Polymer Networks

    NARCIS (Netherlands)

    Lu, W.; Sculley, J.P.; Yuan, D.; Krishna, R.; Zhou, H.C.

    2013-01-01

    Amine-grafted porous polymer networks were investigated for CO2 capture directly from air (400 ppm CO2, 78.96% N-2, and 21% O-2). Under these ultradilute conditions, PPN-6-CH(2)DETA has an extraordinarily high CO2 selectivity (3.6 x 10(10)) and loading capacity (1.04 mol/kg) as calculated using

  13. Numerical modelling of porous cement-based materials by superabsorbent polymers

    DEFF Research Database (Denmark)

    Viejo, Ismael; Esteves, Luis Pedro; Laspalas, Manuel;

    2016-01-01

    The development of new cementitious materials raises new challenges with regard to structural design. One of the potential applications of superabsorbent polymers (SAP) is to deliver well-defined porosity to cement systems. This is particularly interesting for the development of porous cement...

  14. Natural Gas Purification Using a Porous Coordination Polymer with Water and Chemical Stability

    NARCIS (Netherlands)

    Duan, J.; Jin, W.; Krishna, R.

    2015-01-01

    Porous coordination polymers (PCPs), constructed by bridging the metals or clusters and organic linkers, can provide a functional pore environment for gas storage and separation. But the rational design for identifying PCPs with high efficiency and low energy cost remains a challenge. Here, we demon

  15. CONTROL OF POLYMER PARTICLE SIZE USING POROUS GLASS MEMBRANE EMULSIFICATION A REVIEW

    Institute of Scientific and Technical Information of China (English)

    Guanghui Ma

    2003-01-01

    Much attention has in recent years been paid to fine applications of polymer particles, e.g., carrier for enzyme, separation media for protein, DNA and cell, and carrier for drug in Drug Delivery System (DDS). Control of polymer particle size is especially important in such fine applications. For instance, when the particles are used as a carrier of anti-cancer agents, the locations of particles containing anti-cancer agents also depend on the size of the particles. In this paper, various techniques of controlling polymer particle size are described, with emphasis on Shirasu Porous Glass (SPG) membrane emulsification, as carried out in our research group.

  16. Manufacturing a Porous Structure According to the Process Parameters of Functional 3D Porous Polymer Printing Technology Based on a Chemical Blowing Agent

    Science.gov (United States)

    Yoo, C. J.; Shin, B. S.; Kang, B. S.; Yun, D. H.; You, D. B.; Hong, S. M.

    2017-09-01

    In this paper, we propose a new porous polymer printing technology based on CBA(chemical blowing agent), and describe the optimization process according to the process parameters. By mixing polypropylene (PP) and CBA, a hybrid CBA filament was manufactured; the diameter of the filament ranged between 1.60 mm and 1.75 mm. A porous polymer structure was manufactured based on the traditional fused deposition modelling (FDM) method. The process parameters of the three-dimensional (3D) porous polymer printing (PPP) process included nozzle temperature, printing speed, and CBA density. Porosity increase with an increase in nozzle temperature and CBA density. On the contrary, porosity increase with a decrease in the printing speed. For porous structures, it has excellent mechanical properties. We manufactured a simple shape in 3D using 3D PPP technology. In the future, we will study the excellent mechanical properties of 3D PPP technology and apply them to various safety fields.

  17. Solid polymer electrolyte composite membrane comprising plasma etched porous support

    Science.gov (United States)

    Liu, Han; LaConti, Anthony B.

    2010-10-05

    A solid polymer electrolyte composite membrane and method of manufacturing the same. According to one embodiment, the composite membrane comprises a rigid, non-electrically-conducting support, the support preferably being a sheet of polyimide having a thickness of about 7.5 to 15 microns. The support has a plurality of cylindrical pores extending perpendicularly between opposing top and bottom surfaces of the support. The pores, which preferably have a diameter of about 0.1 to 5 microns, are made by plasma etching and preferably are arranged in a defined pattern, for example, with fewer pores located in areas of high membrane stress and more pores located in areas of low membrane stress. The pores are filled with a first solid polymer electrolyte, such as a perfluorosulfonic acid (PFSA) polymer. A second solid polymer electrolyte, which may be the same as or different than the first solid polymer electrolyte, may be deposited over the top and/or bottom of the first solid polymer electrolyte.

  18. USE OF POROUS BIODEGRADABLE POLYMER IMPLANTS IN MENISCUS RECONSTRUCTION .2. BIOLOGICAL EVALUATION OF POROUS BIODEGRADABLE POLYMER IMPLANTS IN MENISCI

    NARCIS (Netherlands)

    ELEMA, H; DEGROOT, JH; NIJENHUIS, AJ; PENNINGS, AJ; VETH, RPH; JANSEN, HWB

    1990-01-01

    Several series of porous, biodegradable PU/PLLA foams were used for meniscus reconstruction in dogs. PLLA-fiber reinforced PU/PLLA composites, PU/PLLA, and PU foams were implanted in severe meniscus lesions. The healing process was initiated as a result of blood vessels' and other cells' ingrowth in

  19. Novel lubricated surface of titanium alloy based on porous structure and hydrophilic polymer brushes

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Kun; Xiong, Dangsheng, E-mail: xiongds@163.com; Niu, Yuxiang

    2014-10-30

    Graphical abstract: - Highlights: • Lubricated Ti6Al4V was fabricated by anodic oxidation and hydrophilic polymer grafting. • Surface composition and tribological properties were estimated. • Proper surface micropores formed at optimum voltage of 100 V. • Combined effect of porous structure and polymer brushes decreased friction coefficient and wear. • Hydrated lubricating layer and hydrodynamic lubrication contributed to lubricated surface. - Abstract: On the purpose of improving the tribological properties of titanium alloy through mimicking natural articular cartilage, porous structure was prepared on the surface of Ti6Al4V alloy by anodic oxidation method, and then hydrophilic polymer brushes were grafted onto its surface. Surface morphology of porous oxidized film was investigated by metalloscope and scanning electron microscope (SEM). The composition and structure of modified surface were characterized by Fourier-transform infrared spectroscopy with attenuated total reflection (FTIR/ATR), and the wettability was also evaluated. Friction and wear properties of modified alloys sliding against ultra-high molecular weight polyethylene (UHMWPE) were tested by a pin-on-disc tribometer in physiological saline. The results showed that, the optimum porous structure treated by anodic oxidation formed when the voltage reached as high as 100 V. Hydrophilic monomers [Acrylic acid (AA) and 3-dimethyl-(3-(N-methacrylamido) propyl) ammonium propane sulfonate (DMMPPS)] were successfully grafted onto porous Ti6Al4V surface to form polymer brushes by UV radiation. The change of contact angle showed that wettability of modified Ti6Al4V was improved significantly. The friction coefficient of modified Ti6Al4V was much lower and more stable than untreated ones. The lowest friction coefficient was obtained when the sample was anodized at 100 V and grafted with DMMPPS, and the value was 0.132. The wear of modified samples was also obviously improved.

  20. Mechanisms of chain adsorption on porous substrates and critical conditions of polymer chromatography.

    Science.gov (United States)

    Cimino, Richard T; Rasmussen, Christopher J; Brun, Yefim; Neimark, Alexander V

    2016-11-01

    Polymer adsorption is a ubiquitous phenomenon with numerous technological and healthcare applications. The mechanisms of polymer adsorption on surfaces and in pores are complex owing to a competition between various entropic and enthalpic factors. Due to adsorption of monomers to the surface, the chain gains in enthalpy yet loses in entropy because of confining effects. This competition leads to the existence of critical conditions of adsorption when enthalpy gain and entropy loss are in balance. The critical conditions are controlled by the confining geometry and effective adsorption energy, which depends on the solvent composition and temperature. This phenomenon has important implications in polymer chromatography, since the retention at the critical point of adsorption (CPA) is chain length independent. However, the mechanisms of polymer adsorption in pores are poorly understood and there is an ongoing discussion in the theoretical literature about the very existence of CPA for polymer adsorption on porous substrates. In this work, we examine the mechanisms of chain adsorption on a model porous substrate using Monte Carlo (MC) simulations. We distinguish three adsorption mechanisms depending on the chain location: on external surface, completely confined in pores, and also partially confined in pores in so-called "flower" conformations. The free energies of different conformations of adsorbed chains are calculated by the incremental gauge cell MC method that allows one to determine the partition coefficient as a function of the adsorption potential, pore size, and chain length. We confirm the existence of the CPA for chain length independent separation on porous substrates, which is explained by the dominant contributions of the chain adsorption at the external surface, in particular in flower conformations. Moreover, we show that the critical conditions for porous and nonporous substrates are identical and depend only on the surface chemistry. The theoretical

  1. Modeling of photocurrent in dye-sensitized solar cells fabricated with PVDF-HFP-based gel-type polymeric solid electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Yoshinori, Nishikitani; Takaya, Kubo; Tsuyoshi, Asano [Central Technical Research Laboratory, Nippon Oil Corporation, Naka-ku, Yokohama (Japan)

    2006-05-15

    We discussed photocurrent of dye-sensitized solar cells (DSCs) with model equations of polymeric solid electrolyte (PSE)-based and liquid electrolyte-based DSCs. The short-circuit current (J{sub sc}) was found out to increase even further by either increasing the diffusion coefficient of I{sub 3}{sup -} and/or I{sup -} or decreasing the cell-gap, or both. In particular, the cell-gap dependence of J{sub sc} indicates clearly that narrowing the cell-gap is a simple, effective way to increase the J{sub sc}. We also discussed the diffusion coefficient dependence of J{sub sc}. The back electron transfer from TiO{sub 2} to an oxidized dye was taken into account and explained the diffusion coefficient dependence of J{sub sc} well. (authors)

  2. Distributed Pore Chemistry in Porous Organic Polymers in Tissue Culture Flasks

    Science.gov (United States)

    Koontz, Steven L. (Inventor)

    1999-01-01

    A method for making a biocompatible polymer article using a uniform atomic oxygen treatment is disclose. The substrate may be subsequently optionally grated with a compatibilizing compound. Compatibilizing compounds may include proteins, phosphorylcholine groups, platelet adhesion preventing polymers, albumin adhesion promoters, and the like. The compatibilized substrate may also have a living cell layer adhered thereto. The atomic oxygen is preferably produced by a flowing afterglow microwave discharge, wherein the substrate resides in a sidearm out of the plasma. Also, methods for culturing cells for various purposes using the various membranes are disclosed as well. Also disclosed are porous organic polymers having a distributed pore chemistry (DPC) comprising hydrophilic and hydrophobic regions, and a method for making the DPC by exposing the polymer to atomic oxygen wherein the rate of hydrophilization is greater than the rate of mass loss.

  3. Bioinspired porous membranes containing polymer nanoparticles for wound healing.

    Science.gov (United States)

    Ferreira, Ana M; Mattu, Clara; Ranzato, Elia; Ciardelli, Gianluca

    2014-12-01

    Skin damages covering a surface larger than 4 cm(2) require a regenerative strategy based on the use of appropriate wound dressing supports to facilitate the rapid tissue replacement and efficient self-healing of the lost or damaged tissue. In the present work, A novel biomimetic approach is proposed for the design of a therapeutic porous construct made of poly(L-lactic acid) (PLLA) fabricated by thermally induced phase separation (TIPS). Biomimicry of ECM was achieved by immobilization of type I collagen through a two-step plasma treatment for wound healing. Anti-inflammatory (indomethacin)-containing polymeric nanoparticles (nps) were loaded within the porous membranes in order to minimize undesired cell response caused by post-operative inflammation. The biological response to the scaffold was analyzed by using human keratinocytes cell cultures. In this work, a promising biomimetic construct for wound healing and soft tissue regeneration with drug-release properties was fabricated since it shows (i) proper porosity, pore size, and mechanical properties, (ii) biomimicry of ECM, and (iii) therapeutic potential. © 2014 Wiley Periodicals, Inc.

  4. Integration of monolithic porous polymer with droplet-based microfluidics on a chip for nano/picoliter volume sample analysis

    OpenAIRE

    Kim, Jin-Young; Chang, Soo-Ik; Andrew J deMello; O’Hare, Danny

    2014-01-01

    In this paper, a porous polymer nanostructure has been integrated with droplet-based microfluidics in a single planar format. Monolithic porous polymer (MPP) was formed selectively within a microfluidic channel. The resulting analyte bands were sequentially comartmentalised into droplets. This device reduces band broadening and the effects of post-column dead volume by the combination of the two techniques. Moreover it offers the precise control of nano/picoliter volume samples.

  5. Porous Silicon and Polymer Nanocomposites for Delivery of Peptide Nucleic Acids as Anti-MicroRNA Therapies.

    Science.gov (United States)

    Beavers, Kelsey R; Werfel, Thomas A; Shen, Tianwei; Kavanaugh, Taylor E; Kilchrist, Kameron V; Mares, Jeremy W; Fain, Joshua S; Wiese, Carrie B; Vickers, Kasey C; Weiss, Sharon M; Duvall, Craig L

    2016-09-01

    Self-assembled polymer/porous silicon nanocomposites overcome intracellular and systemic barriers for in vivo application of peptide nucleic acid (PNA) anti-microRNA therapeutics. Porous silicon (PSi) is leveraged as a biodegradable scaffold with high drug-cargo-loading capacity. Functionalization with a diblock polymer improves PSi nanoparticle colloidal stability, in vivo pharmacokinetics, and intracellular bioavailability through endosomal escape, enabling PNA to inhibit miR-122 in vivo.

  6. A porous polymer scaffold for meniscal lesion repair--a study in dogs.

    Science.gov (United States)

    Tienen, T G; Heijkants, R G J C; Buma, P; De Groot, J H; Pennings, A J; Veth, R P H

    2003-06-01

    Meniscal lesions often occur in the avascular area of the meniscus with little chance of spontaneous repair. An access channel in the meniscal tissue can function as an entrance for ingrowing repair tissue from the vascular periphery of the meniscus to the lesion in the avascular zone which again induced healing of the lesion. Implantation of a porous polymer in a full-thickness access channel induced healing. However, a better integration between meniscal tissue and the implant might be achieved with the combination of the newly developed porous polymers and a modified surgical technique. This might improve meniscal lesion healing and the repair of the access channel with neo-meniscal tissue. Longitudinal lesions were created in the avascular part of 24 canine lateral menisci and a partial-thickness access channel was formed to connect the lesion with the meniscal periphery. In 12 menisci, the access channel was left empty (control group), while in the remaining 12 menisci the polymer implant was sutured into the access channel. Repair of the longitudinal lesions was achieved with and without polymer implantation in the partial-thickness access channel. Polymer implants induced fibrous ingrowth with cartilaginous areas, which resembled neo-meniscal tissue. Implantation did not prevent articular cartilage degeneration.

  7. Method of Manufacturing A Porous Polymer Component Involving Use of A Dissolvable, Sacrificial Material

    OpenAIRE

    Mohanty, Soumyaranjan; Emnéus, Jenny; Wolff, Anders; Dufva, Martin; Larsen, Layla Bashir; Skolimowski, Maciej; Amato, Letizia

    2015-01-01

    The present invention relates to a method of manufacturing a porous polymer component 1 with structured and/or random pores 4 and/or channels 5. The method comprises arranging a dissolvable, sacrificial material 2 in a geometrical arrangement corresponding to an inner structure to be obtained in the polymer component 1. A component material 3, which is to form the final component 1, is arranged so that it surrounds at least a majority of the sacrificial material 2, and subsequently the sacrif...

  8. Dye-sensitized solar cells based on porous conjugated polymer counter electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Torabi, Naeimeh; Behjat, Abbas, E-mail: abehjat@yazd.ac.ir; Jafari, Fatemeh

    2014-12-31

    In this paper, we report platinum-free dye-sensitized solar cells that were fabricated using a grown porous poly-3-methyl-thiophene (P3MT) counter electrode. The growing of the porous P3MT was performed by an electrochemical deposition method. This method is easy and affordable unlike the common expensive deposition methods. The morphology of P3MT films was studied by scanning electron microscopy images. It was observed that polymer layers grown with a current density of 2 mA/cm{sup 2} have a clear porous and rough structure as compared to layers grown with a lower current density. To understand the reaction kinetics and the catalytic activities of the counter electrodes with P3MT for 3I{sup −}/I{sub 3}{sup −} redox reaction, cyclic voltammetry (CV) was performed. Based on the analysis of CV, it was shown that this layer can be used as a counter electrode for dye-sensitized solar cells. The electro deposition conditions during the growth of polymer layers such as current density, the morphology of polymer films and the duration of polymerization have a significant role in the current–voltage characterization of the fabricated solar cells. The performance of the fabricated solar cells was improved by optimization of these parameters. The highest efficiency of 2.76% was obtained by using porous P3MT in the counter electrode. - Highlights: • Poly-3-methyl-thiophene (P3MT) layers were grown using electrochemical deposition method. • By controlling the growth conditions, porous P3MT can be produced. • Grown P3MT layers can be used as counter electrodes in dye-sensitized solar cells. • The growth rate of P3MT layers plays an essential role in the cell performance.

  9. Synthesis of three-dimensional porous hyper-crosslinked polymers via thiol–yne reaction

    Directory of Open Access Journals (Sweden)

    Mathias Lang

    2016-11-01

    Full Text Available Herein we report the syntheses of two porous hyper-crosslinked polymers (HCPs via thiol–yne reaction with rigid tetrahedral and pseudo-octahedral core structures. Sorption measurements with nitrogen gas at 77 K revealed BET-surface areas up to 650 m²/g. Those networks also showed a high thermal stability as well as insolubility in common organic solvents.

  10. Trypsin immobilization in ordered porous polymer membranes for effective protein digestion

    Energy Technology Data Exchange (ETDEWEB)

    Qiao, Juan [Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, No. 2 Zhongguancun Beiyijie, Beijing 100190 (China); Kim, Jin Yong [Department of Chemistry, Yonsei University, 50 Yonsei-ro, Seoul 120-749 (Korea, Republic of); Wang, Yuan Yuan [Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, No. 2 Zhongguancun Beiyijie, Beijing 100190 (China); Qi, Li, E-mail: qili@iccas.ac.cn [Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, No. 2 Zhongguancun Beiyijie, Beijing 100190 (China); Wang, Fu Yi [Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, No. 2 Zhongguancun Beiyijie, Beijing 100190 (China); Moon, Myeong Hee, E-mail: mhmoon@yonsei.ac.kr [Department of Chemistry, Yonsei University, 50 Yonsei-ro, Seoul 120-749 (Korea, Republic of)

    2016-02-04

    Fast and effective protein digestion is a vital process for mass spectrometry (MS) based protein analysis. This study introduces a porous polymer membrane enzyme reactor (PPMER) coupled to nanoflow liquid chromatography-tandem MS (nLC-ESI-MS/MS) for on-line digestion and analysis of proteins. Poly (styrene-co-maleic anhydride) (PS-co-MAn) was fabricated by the breath figure method to make a porous polymer membrane in which the MAn group was covalently bound to enzyme. Based on this strategy, microscale PPMER (μPPMER) was constructed for on-line connection with the nLC-ESI-MS/MS system. Its capability for enzymatic digestion with bovine serum albumin (BSA) was evaluated with varied digestion periods. The on-line proteolysis of BSA and subsequent analysis with μPPMER-nLC-ESI-MS/MS revealed that peptide sequence coverage increased from 10.3% (digestion time 10 min) to 89.1% (digestion time 30 min). μPPMER can efficiently digest proteins due to the microscopic confinement effect, showing its potential application in fast protein identification and protease immobilization. Applications of on-line digestion using μPPMER with human plasma and urinary proteome samples showed that the developed on-line method yielded equivalent or better performance in protein coverage and identified more membrane proteins than the in-solution method. This may be due to easy accommodation of hydrophobic membrane proteins within membrane pores. - Highlights: • A porous polymer membrane enzyme reactor was developed. • Breath figure method was used for the fabrication of porous polymer membrane. • The enzyme reactor was coupled to nLC-ESI-MS/MS for proteins on-line digestion.

  11. Porous cationic polymers: the impact of counteranions and charges on CO2 capture and conversion.

    Science.gov (United States)

    Buyukcakir, Onur; Je, Sang Hyun; Choi, Dong Shin; Talapaneni, Siddulu Naiudu; Seo, Yongbeom; Jung, Yousung; Polychronopoulou, Kyriaki; Coskun, Ali

    2016-01-18

    Porous cationic polymers (PCPs) with surface areas up to 755 m(2) g(-1) bearing positively charged viologen units in their backbones and different counteranions have been prepared. We have demonstrated that by simply varying counteranions both gas sorption and catalytic properties of PCPs can be tuned for metal-free capture and conversion of CO2 into value-added products such as cyclic carbonates with excellent yields.

  12. Hydrophobic liquid-infused porous polymer surfaces for antibacterial applications.

    Science.gov (United States)

    Li, Junsheng; Kleintschek, Tanja; Rieder, Annika; Cheng, Yin; Baumbach, Tilo; Obst, Ursula; Schwartz, Thomas; Levkin, Pavel A

    2013-07-24

    Biofilms represent a fundamental problem in environmental biology, water technology, food hygiene as well as in medical and technical systems. Recently introduced slippery liquid-infused porous surface (SLIPS) showed great promise for preventing biofilm formation owing to the low surface energy of such surface in combination with its self-cleaning properties. In this study we demonstrated a novel hydrophobic liquid-infused porous poly(butyl methacrylate-co-ethylene dimethacrylate) surface (slippery BMA-EDMA) with bacteria-resistance in BM2 mineral medium and long-term stability in aqueous environments. We showed that the slippery BMA-EDMA surface prevents biofilm formation of different strains of opportunistic pathogen Pseudomonas aeruginosa for at least up to 7 days in low nutrient medium. Only ∼1.8% of the slippery surface was covered by the environmental P. aeruginosa PA49 strain under investigation. In uncoated glass controls the coverage of surfaces reached ∼55% under the same conditions. However, in high nutrient medium, more relevant to physiological conditions, the biofilm formation on the slippery surface turned out to be highly dependent on the bacterial strain. Although the slippery surface could prevent biofilm formation of most of the P. aeruginosa strains tested (∼1% surface coverage), the multiresistant P. aeruginosa strain isolated from wastewater was able to cover up to 12% of the surface during 7 days of incubation. RAPD-PCR analysis of the used P. aeruginosa strains demonstrated their high genome variability, which might be responsible for their difference in biofilm formation on the slippery BMA-EDMA surface. The results show that although the slippery BMA-EDMA surface has a great potential against biofilm formation, the generality of its bacteria resistant properties is still to be improved.

  13. Towards a methodology for the effective surface modification of porous polymer scaffolds.

    Science.gov (United States)

    Safinia, Laleh; Datan, Nathalie; Höhse, Marek; Mantalaris, Athanassios; Bismarck, Alexander

    2005-12-01

    A novel low-pressure radio-frequency plasma treatment protocol was developed to achieve the effective through-thickness surface modification of large porous poly (D,L-lactide) (PDLLA) polymer scaffolds using air or water: ammonia plasma treatments. Polymer films were modified as controls. Scanning electron micrographs and maximum bubble point measurements demonstrated that the PDLLA foams have the high porosity, void fraction and interconnected pores required for use as tissue engineering scaffolds. The polymer surface of the virgin polymer does contain acidic functional groups but is hydrophobic. Following exposure to air or water: ammonia plasma, an increased number of polar functional groups and improved wetting behaviour, i.e. hydrophilicity, of wet surfaces was detected. The number of polar surface functional groups increased (hence the decrease in water contact angles) with increasing exposure time to plasma. The change in surface composition and wettablility of wet polymer constructs was characterised by zeta potential and contact angle measurements. The hydrophobic recovery of the treated PDLLA polymer surfaces was also studied. Storage of the treated polymer constructs in ambient air caused an appreciable hydrophobic recovery, whereas in water only partial hydrophobic recovery occurred. However, in both cases the initial surface characteristics decay as function of time.

  14. Light emitting composite rods based on porous silicon in ormosils and polymer matrices for optical applications

    Science.gov (United States)

    Naziruddin Khan, M.; Al Dwayyan, A. S.; Aldalbahi, Ali

    2017-06-01

    Porous silicon (PSi) colloidal solution was directly encapsulated in ormosils and polymer sols to develop nanocomposite based rods. PSi is highly crystalline of around 5-8 nm particles size confirmed by Transmission electron microscopy. SEM images indicate that structural morphology of PSi in the ormosils and polymer environment are different. No major effect on infrared property of PSi particles in the Ormosils and polymers are observed. Absorption and emission property of PSi is influenced when the PSi combined in Ormosils and polymer matrix. Significant photoluminescence stability of PSi in the both matrices is found. Subsequently the spontaneous emission of polished PSi composite ormosils and polymer rods were studied under the pico second tunable laser source. The exhibited spontaneous emission is quite significant. Remarkable stability and optically active of PSi particles in polymer over the ormosils is observed over time. Such composites based on PSi in ormosils and polymer may possibly be improved if high concentration of colloidal solution is employed for further optical test under laser.

  15. Honeycomb-like porous gel polymer electrolyte membrane for lithium ion batteries with enhanced safety

    Science.gov (United States)

    Zhang, Jinqiang; Sun, Bing; Huang, Xiaodan; Chen, Shuangqiang; Wang, Guoxiu

    2014-08-01

    Lithium ion batteries have shown great potential in applications as power sources for electric vehicles and large-scale energy storage. However, the direct uses of flammable organic liquid electrolyte with commercial separator induce serious safety problems including the risk of fire and explosion. Herein, we report the development of poly(vinylidene difluoride-co-hexafluoropropylene) polymer membranes with multi-sized honeycomb-like porous architectures. The as-prepared polymer electrolyte membranes contain porosity as high as 78%, which leads to the high electrolyte uptake of 86.2 wt%. The PVDF-HFP gel polymer electrolyte membranes exhibited a high ionic conductivity of 1.03 mS cm-1 at room temperature, which is much higher than that of commercial polymer membranes. Moreover, the as-obtained gel polymer membranes are also thermally stable up to 350°C and non-combustible in fire (fire-proof). When applied in lithium ion batteries with LiFePO4 as cathode materials, the gel polymer electrolyte demonstrated excellent electrochemical performances. This investigation indicates that PVDF-HFP gel polymer membranes could be potentially applicable for high power lithium ion batteries with the features of high safety, low cost and good performance.

  16. Aerogels of 1D Coordination Polymers: From a Non-Porous Metal-Organic Crystal Structure to a Highly Porous Material

    Directory of Open Access Journals (Sweden)

    Adrián Angulo-Ibáñez

    2016-01-01

    Full Text Available The processing of an originally non-porous 1D coordination polymer as monolithic gel, xerogel and aerogel is reported as an alternative method to obtain novel metal-organic porous materials, conceptually different to conventional crystalline porous coordination polymer (PCPs or metal-organic frameworks (MOFs. Although the work herein reported is focused upon a particular kind of coordination polymer ([M(μ-ox(4-apy2]n, M: Co(II, Ni(II, the results are of interest in the field of porous materials and of MOFs, as the employed synthetic approach implies that any coordination polymer could be processable as a mesoporous material. The polymerization conditions were fixed to obtain stiff gels at the synthesis stage. Gels were dried at ambient pressure and at supercritical conditions to render well shaped monolithic xerogels and aerogels, respectively. The monolithic shape of the synthesis product is another remarkable result, as it does not require a post-processing or the use of additives or binders. The aerogels of the 1D coordination polymers are featured by exhibiting high pore volumes and diameters ranging in the mesoporous/macroporous regions which endow to these materials the ability to deal with large-sized molecules. The aerogel monoliths present markedly low densities (0.082–0.311 g·cm−3, an aspect of interest for applications that persecute light materials.

  17. Enhancement of Li+ ion conductivity in solid polymer electrolytes using surface tailored porous silica nanofillers

    Science.gov (United States)

    Mohanta, Jagdeep; Singh, Udai P.; Panda, Subhendu K.; Si, Satyabrata

    2016-09-01

    The current study represents the design and synthesis of polyethylene oxide (PEO)-based solid polymer electrolytes by solvent casting approach using surface tailored porous silica as nanofillers. The surface tailoring of porous silica nanostructure is achieved through silanization chemistry using 3-glycidyloxypropyl trimethoxysilane in which silane part get anchored to the silica surface whereas epoxy group get stellated from the silica surface. Surface tailoring of silica with epoxy group increases the room temperature electrochemical performances of the resulting polymer electrolytes. Ammonical hydrolysis of organosilicate precursor is used for both silica preparation and their surface tailoring. The composite solid polymer electrolyte films are prepared by solution mixing of PEO with lithium salt in presence of silica nanofillers and cast into film by solvent drying, which are then characterized by impedance measurement for conductivity study and wide angle x-ray diffraction for change in polymer crystallinity. Room temperature impedance measurement reveals Li+ ion conductivity in the order of 10-4 S cm-1, which is correlated to the decrease in PEO crystallinity. The enhancement of conductivity is further observed to be dependent on the amount of silica as well as on their surface characteristics.

  18. 21 CFR 888.3535 - Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Knee joint femorotibial (uni-compartmental) metal... Devices § 888.3535 Knee joint femorotibial (uni-compartmental) metal/polymer porous-coated uncemented prosthesis. (a) Identification. A knee joint femorotibial (uni-compartmental) metal/polymer...

  19. Chemical structure, synthesis, and physical and chemical properties of porous polymers as materials applied in analytical chemistry and environmental protection

    Directory of Open Access Journals (Sweden)

    Goś Piotr

    2016-12-01

    Full Text Available This article is part of a series devoted to discussing strategies for the synthesis of ion-imprinted polymers and molecularly imprinted polymers, their chemical structure and great potential, which may be used in porous material design, analytical chemistry, environmental protection and other areas of science. The presented work constitutes a basis for a better understanding of what porous polymers are, how we can synthesise them and how to foresee their properties, which can be later used in studies of environmental pollution and analytical chemistry.

  20. Rapid removal of organic micropollutants from water by a porous β-cyclodextrin polymer

    Science.gov (United States)

    Alsbaiee, Alaaeddin; Smith, Brian J.; Xiao, Leilei; Ling, Yuhan; Helbling, Damian E.; Dichtel, William R.

    2016-01-01

    The global occurrence in water resources of organic micropollutants, such as pesticides and pharmaceuticals, has raised concerns about potential negative effects on aquatic ecosystems and human health. Activated carbons are the most widespread adsorbent materials used to remove organic pollutants from water but they have several deficiencies, including slow pollutant uptake (of the order of hours) and poor removal of many relatively hydrophilic micropollutants. Furthermore, regenerating spent activated carbon is energy intensive (requiring heating to 500-900 degrees Celsius) and does not fully restore performance. Insoluble polymers of β-cyclodextrin, an inexpensive, sustainably produced macrocycle of glucose, are likewise of interest for removing micropollutants from water by means of adsorption. β-cyclodextrin is known to encapsulate pollutants to form well-defined host-guest complexes, but until now cross-linked β-cyclodextrin polymers have had low surface areas and poor removal performance compared to conventional activated carbons. Here we crosslink β-cyclodextrin with rigid aromatic groups, providing a high-surface-area, mesoporous polymer of β-cyclodextrin. It rapidly sequesters a variety of organic micropollutants with adsorption rate constants 15 to 200 times greater than those of activated carbons and non-porous β-cyclodextrin adsorbent materials. In addition, the polymer can be regenerated several times using a mild washing procedure with no loss in performance. Finally, the polymer outperformed a leading activated carbon for the rapid removal of a complex mixture of organic micropollutants at environmentally relevant concentrations. These findings demonstrate the promise of porous cyclodextrin-based polymers for rapid, flow-through water treatment.

  1. Rapid removal of organic micropollutants from water by a porous β-cyclodextrin polymer.

    Science.gov (United States)

    Alsbaiee, Alaaeddin; Smith, Brian J; Xiao, Leilei; Ling, Yuhan; Helbling, Damian E; Dichtel, William R

    2016-01-14

    The global occurrence in water resources of organic micropollutants, such as pesticides and pharmaceuticals, has raised concerns about potential negative effects on aquatic ecosystems and human health. Activated carbons are the most widespread adsorbent materials used to remove organic pollutants from water but they have several deficiencies, including slow pollutant uptake (of the order of hours) and poor removal of many relatively hydrophilic micropollutants. Furthermore, regenerating spent activated carbon is energy intensive (requiring heating to 500-900 degrees Celsius) and does not fully restore performance. Insoluble polymers of β-cyclodextrin, an inexpensive, sustainably produced macrocycle of glucose, are likewise of interest for removing micropollutants from water by means of adsorption. β-cyclodextrin is known to encapsulate pollutants to form well-defined host-guest complexes, but until now cross-linked β-cyclodextrin polymers have had low surface areas and poor removal performance compared to conventional activated carbons. Here we crosslink β-cyclodextrin with rigid aromatic groups, providing a high-surface-area, mesoporous polymer of β-cyclodextrin. It rapidly sequesters a variety of organic micropollutants with adsorption rate constants 15 to 200 times greater than those of activated carbons and non-porous β-cyclodextrin adsorbent materials. In addition, the polymer can be regenerated several times using a mild washing procedure with no loss in performance. Finally, the polymer outperformed a leading activated carbon for the rapid removal of a complex mixture of organic micropollutants at environmentally relevant concentrations. These findings demonstrate the promise of porous cyclodextrin-based polymers for rapid, flow-through water treatment.

  2. Thermal diffusivity measurements on porous carbon fiber reinforced polymer tubes

    Science.gov (United States)

    Gruber, Jürgen; Gresslehner, Karl Heinz; Mayr, Günther; Hendorfer, Günther

    2017-02-01

    This work presents the application of methods for the determination of the thermal diffusivity well suited for flat bodies adapted to cylindrical bodies. Green's functions were used to get the temperature time history for small and large times, for the approach of intersecting these two straight lines. To verify the theoretical considerations noise free data are generated by finite element simulations. Furthermore effects of inhomogeneous excitation and the anisotropic heat conduction of carbon fiber reinforced polymers were taken into account in these numerical simulations. It could be shown that the intersection of the two straight lines is suitable for the determination of the thermal diffusivity, although the results have to be corrected depending on the ratio of the cylinders inner and outer radii. Inhomogeneous excitation affects the results of this approach as it lead to multidimensional heat flux. However, based on the numerical simulations a range of the azimuthal angle exists, where the thermal diffusivity is nearly independent of the angle. The method to determine the thermal diffusivity for curved geometries by the well suited Thermographic Signal Reconstruction method and taking into account deviations from the slab by a single correction factor has great advantages from an industrial point of view, just like an easy implementation into evaluation software and the Thermographic Signal Reconstruction methods rather short processing time.

  3. Polymer composites and porous materials prepared by thermally induced phase separation and polymer-metal hybrid methods

    Science.gov (United States)

    Yoon, Joonsung

    The primary objective of this research is to investigate the morphological and mechanical properties of composite materials and porous materials prepared by thermally induced phase separation. High melting crystallizable diluents were mixed with polymers so that the phase separation would be induced by the solidification of the diluents upon cooling. Theoretical phase diagrams were calculated using Flory-Huggins solution thermodynamics which show good agreement with the experimental results. Porous materials were prepared by the extraction of the crystallized diluents after cooling the mixtures (hexamethylbenzene/polyethylene and pyrene/polyethylene). Anisotropic structures show strong dependence on the identity of the diluents and the composition of the mixtures. Anisotropic crystal growth of the diluents was studied in terms of thermodynamics and kinetics using DSC, optical microscopy and SEM. Microstructures of the porous materials were explained in terms of supercooling and dendritic solidification. Dual functionality of the crystallizable diluents for composite materials was evaluated using isotactic polypropylene (iPP) and compatible diluents that crystallize upon cooling. The selected diluents form homogeneous mixtures with iPP at high temperature and lower the viscosity (improved processability), which undergo phase separation upon cooling to form solid particles that function as a toughening agent at room temperature. Tensile properties and morphology of the composites showed that organic crystalline particles have the similar effect as rigid particles to increase toughness; de-wetting between the particle and iPP matrix occurs at the early stage of deformation, followed by unhindered plastic flow that consumes significant amount of fracture energy. The effect of the diluents, however, strongly depends on the identity of the diluents that interact with the iPP during solidification step, which was demonstrated by comparing tetrabromobisphenol-A and

  4. Data on bone marrow stem cells delivery using porous polymer scaffold

    Directory of Open Access Journals (Sweden)

    Ramasatyaveni Geesala

    2016-03-01

    Full Text Available Low bioavailability and/or survival at the injury site of transplanted stem cells necessitate its delivery using a biocompatible, biodegradable cell delivery vehicle. In this dataset, we report the application of a porous biocompatible, biodegradable polymer network that successfully delivers bone marrow stem cells (BMSCs at the wound site of a murine excisional splint wound model. In this data article, we are providing the additional data of the reference article “Porous polymer scaffold for on-site delivery of stem cells – protects from oxidative stress and potentiates wound tissue repair” (Ramasatyaveni et al., 2016 [1]. This data consists of the characterization of bone marrow stem cells (BMSCs showing the pluripotency and stem cell-specific surface markers. Image analysis of the cellular penetration into PEG–PU polymer network and the mechanism via enzymatic activation of MMP-2 and MMP-13 are reported. In addition, we provide a comparison of various routes of transplantation-mediated BMSCs engraftment in the murine model using bone marrow transplantation chimeras. Furthermore, we included in this dataset the engraftment of BMSCs expressing Sca-1+Lin−CD133+CD90.2+ in post-surgery day 10.

  5. Trapping of a spatial transient state during the framework transformation of a porous coordination polymer.

    Science.gov (United States)

    Kondo, Mio; Furukawa, Shuhei; Hirai, Kenji; Tsuruoka, Takaaki; Reboul, Julien; Uehara, Hiromitsu; Diring, Stéphane; Sakata, Yoko; Sakata, Osami; Kitagawa, Susumu

    2014-04-01

    Structural transformability accompanied by molecular accommodation is a distinguished feature of porous coordination polymers (PCPs) among porous materials. Conventional X-ray crystallography allows for the determination of each structural phase emerged during transformation. However, the propagation mechanism of transformation through an entire crystal still remains in question. Here we elucidate the structural nature of the spatial transient state, in which two different but correlated framework structures, an original phase and a deformed phase, simultaneously exist in one crystal. The deformed phase is distinctively generated only at the crystal surface region by introducing large guest molecules, while the remaining part of crystal containing small molecules maintains the original phase. By means of grazing incidence diffraction techniques we determine that the framework is sheared with sharing one edge of the original primitive cubic structure, leading to the formation of crystal domains with four mirror image relationships.

  6. Structure of porous electrodes in polymer electrolyte membrane fuel cells: An optical reconstruction technique

    Science.gov (United States)

    Berejnov, Viatcheslav; Sinton, David; Djilali, Ned

    Computing flows and phase transport in porous media requires a physically representative geometric model. We present a simple method of digitizing the structure of fibrous porous media commonly used in polymer electrolyte membrane (PEM) fuel cells, the so-called gas diffusion layer (GDL). Employing an inverted microscope and image recognition software we process images of the GDL surface collected manually at different focal lengths with micrometer accuracy. Processing the series of images allows retrieval of local depths of the salient in-focus structural elements in each of the different images. These elements are then recombined into a depth-map representing the three-dimensional structure of the GDL surface. Superimposition of the in-focus portions of the structural elements distributed throughout the stack of images yields digitized data describing the geometry and structural attributes of the 3D surface of the GDL fibrous material.

  7. Novel thiophene-bearing conjugated microporous polymer honeycomb-like porous spheres with ultrahigh iodine uptake.

    Science.gov (United States)

    Ren, Feng; Zhu, Zhaoqi; Qian, Xin; Liang, Weidong; Mu, Peng; Sun, Hanxue; Liu, Jiehua; Li, An

    2016-07-28

    Two conjugated microporous polymers containing thiophene-moieties (SCMPs) were obtained by the polymerization of 3,3',5,5'-tetrabromo-2,2'-bithiophene and ethynylbenzene monomers through the palladium-catalyzed Sonogashira-Hagihara crosscoupling reaction. The resulting SCMPs show high thermal stability with a decomposition temperature above 300 °C. Scanning electron microscopy images show that the resulting SCMPs formed as an aggregation composed of micrometer-sized SCMP spheres, in which honeycomb-like porous spheres with penetrated pores on the surface were observed. Taking advantage of such a unique honeycomb-like porous morphology as well as π-conjugated structures, the SCMPs show ultrahigh absorption performance for iodine vapour with an uptake of up to 345 wt% obtained, which is the highest value reported to date for CMPs, thus making the resulting SCMPs ideal absorbent materials for reversible iodine capture to address environmental issues.

  8. Effects of Calcination Condition on Porous Reduced Titanium Oxides and Oxynitrides via Preceramic Polymer Route

    Energy Technology Data Exchange (ETDEWEB)

    Hasegawa, George; Sato, Tatsuya; Kanamori, Kazuyoshi; Sun, Cheng-Jun; Ren, Yang; Kobayashi, Yoji; Kageyama, Hiroshi; Abe, Takeshi; Nakanishi, Kazuki

    2015-03-16

    The preceramic polymer route from titanium-based inorganic-organic hybrid networks provides electro conductive N-doped reduced titanium oxides (TinO2n–1) and titanium oxynitrides (TiOxNy) with a monolithic shape as well as well-defined porous structure. This methodology demonstrates advantageously lower temperature of crystal phase transition compared to the reduction of TiO2 by carbon or H2. In this study, effects of calcination condition on various features of the products have been explored by adopting three different atmospheric conditions and varying the calcination temperature. The detailed crystallographic and elemental analyses disclose the distinguished difference in phase transition behavior with respect to calcination atmosphere. Correlation between the crystallization and nitridation behaviors, porous properties and electric conductivities in the final products has been discussed.

  9. A Mathematical Model of Repeated Impregnation of Porous Bodies with Solutions of Polymers

    Directory of Open Access Journals (Sweden)

    I. V. Glebov

    2015-01-01

    Full Text Available The paper describes basic methods of impregnating porous bodies with solutions of polymers and their use to manufacture prepregs. It also describes the existing methods of manufacturing multilayer prepregs to produce aerospace coating of the spacecraft "Soyuz". It is shown that these prepregs have to meet high requirements for the content of the polymer, as compared with other composite materials, about 35 - 40% of the mass. Methods used for their manufacturing are long-term and non-controllable. The assumption is made that using the vacuum impregnation technology of a woven material will allow to accelerate the manufacturing process of these prepregs and improve their quality.In reviewing the technical literature have been found works on modeling the processes of impregnation, but they are aimed only at studying the speed of the woven material impregnation by various fluids and determining the time of impregnation. There were no models found to define prepreg parameters during the process of multiple impregnations. The aim of this work is to develop the simple mathematical model, which enables us to predict the polymer content of volatile products in the prepreg after each cycle of multiple impregnation of woven material with a solution of the polymer.To consider the vacuum impregnation method are used the prepregs based on silica and silica-nylon stitch-bonding fabric and bakelite varnish LBS-4 containing 50 - 60% of phenol resin and the solvent with minor impurities of pure phenol and water, as an example. To describe the process of vacuum impregnation of the porous work-piece is developed a mathematical description of the process of filling the porous space of the material with a varnish. It is assumed that the varnish components fill the porous space of the material in the same proportion as they are contained in the varnish.It is shown that a single impregnation cannot ensure the content of phenol resin in the prepreg over 32%, which does

  10. Selective Adsorption of CO2 from Light Gas Mixtures Using a Structurally Dynamic Porous Coordination Polymer**

    Energy Technology Data Exchange (ETDEWEB)

    Kristi L. Kauffman, Jeffrey T. Culp, Andrew J. Allen, Laura Espinal, Winnie Wong-Ng, Thomas D.

    2010-01-01

    The selective adsorption of CO{sub 2} from mixtures with N{sub 2}, CH{sub 4}, and N{sub 2}O in a dynamic porous coordination polymer (see monomer structure) was evaluated by ATR-FTIR spectroscopy, GC, and SANS. All three techniques indicate highly selective adsorption of CO{sub 2} from CO{sub 2}/CH{sub 4} and CO{sub 2}/N{sub 2} mixtures at 30 C, with no selectivity observed for the CO{sub 2}/N{sub 2}O system.

  11. Evaluation of Metal-Organic Frameworks and Porous Polymer Networks for CO2 -Capture Applications.

    Science.gov (United States)

    Verdegaal, Wolfgang M; Wang, Kecheng; Sculley, Julian P; Wriedt, Mario; Zhou, Hong-Cai

    2016-03-21

    This manuscript presents experimental data for 20 adsorption materials (metal-organic frameworks, porous polymer networks, and Zeolite-5A), including CO2 and N2 isotherms and heat capacities. With input from only experimental data, working capacities per energy for each material were calculated. Furthermore, by running seven different carbon-capture scenarios in which the initial flue-gas composition and process temperature was systematically changed, we present a range of performances for each material and quantify how sensitive each is to these varying parameters. The presented calculations provide researchers with a tool to investigate promising carbon-capture materials more easily and completely.

  12. Spatially isolated palladium in porous organic polymers by direct knitting for versatile organic transformations

    KAUST Repository

    Wang, Xinbo

    2017-10-03

    We report here a direct knitting Method for preparation of highly robust, effective while air- and moisture-tolerant, and readily recyclable three-dimensional (3D) porous polymer-Pd network (PPPd) from the widely used Pd(PPh3)4. Electro-beam induced Pd atom crystallization was observed for the first time in organic polymer and revealed the ultrafine dispersion of palladium atoms. Challenging types of Suzuki-Miyaura couplings, reductive coupling of aryl halides and oxidative coupling of arylboronic acid were successively catalyzed by PPPd in aqueous media. Also catalytically selective CH functionalization reactions were achieved with orders of magnitude more efficient than conventional Pd homogeneous catalysts. The strategy developed here provides a practical method for easy-to-make yet highly efficient heterogeneous catalysis.

  13. Hard coating for polymer substrates through lamination and peeling of porous anodized zirconia.

    Science.gov (United States)

    Masheder, Benjamin

    2014-04-01

    Transparent and hard zirconia (ZrO2) films with thicknesses in the range of 1.5 to 1.8 microm were successfully formed on various polymer surfaces, i.e., polycarbonate (PC), polystyrene (PS), polyethylene terephthalate (PET) and polymethylmethacrylate (PMMA) with excellent adhesion and without cracking, while preserving their bulk properties. Our process is based on a lamination of porous anodized ZrO2 membranes (PAZMs) to the polymer surfaces through capillary action, followed by simple peeling with tweezers to remove the unanodized metal Zr foil. The resulting PAZM-laminated surfaces exhibited excellent surface chemical and physical durability. Our technique also allowed the reuse of a single Zr foil piece multiple times for several anodization and lamination cycles.

  14. Method of Manufacturing A Porous Polymer Component Involving Use of A Dissolvable, Sacrificial Material

    DEFF Research Database (Denmark)

    2015-01-01

    The present invention relates to a method of manufacturing a porous polymer component 1 with structured and/or random pores 4 and/or channels 5. The method comprises arranging a dissolvable, sacrificial material 2 in a geometrical arrangement corresponding to an inner structure to be obtained...... in the polymer component 1. A component material 3, which is to form the final component 1, is arranged so that it surrounds at least a majority of the sacrificial material 2, and subsequently the sacrificial material 2 is dissolved and removed from the component material 3. The sacrificial material 2...... and thereby the resulting inner structure of the component 1 is arranged in a controlled and reproducible manner. The sacrificial material 2 and possibly also the component material 3 may e.g. be arranged by use of a 3D-printer or manually. The method may e.g. be used to manufacture a three...

  15. Compressive behavior and energy absorption of metal porous polymer composite with interpenetrating network structure

    Institute of Scientific and Technical Information of China (English)

    LIU Yu; GONG Xiao-lu

    2006-01-01

    Interpenetrating phase composites (IPCs) are a new class of composite materials with improved combinations of mechanical and physical properties. This study was performed on a new type of IPC called metal porous polymer composite (MPPC) with an interpenetrating network structure. Aluminum-polypropylene (Al-PE) and Aluminum-epoxy resin (Al-Ep) composites were produced by infiltrating the polymer in the aluminum foam. The composite microstructures were characterized using SEM observation. The compressive behavior and energy absorption characteristics of MPPC were investigated and compared with the aluminum foams. The compressive modulus of composite was compared with the VOIGT-REUSS bounds and HASHIN-SHTRIKMAN (H-S) bounds models. The experimental modulus of compressive tests falls well within the theoretical models.

  16. "Thunderstruck": Plasma-Polymer-Coated Porous Silicon Microparticles As a Controlled Drug Delivery System.

    Science.gov (United States)

    McInnes, Steven J P; Michl, Thomas D; Delalat, Bahman; Al-Bataineh, Sameer A; Coad, Bryan R; Vasilev, Krasimir; Griesser, Hans J; Voelcker, Nicolas H

    2016-02-01

    Controlling the release kinetics from a drug carrier is crucial to maintain a drug's therapeutic window. We report the use of biodegradable porous silicon microparticles (pSi MPs) loaded with the anticancer drug camphothecin, followed by a plasma polymer overcoating using a loudspeaker plasma reactor. Homogenous "Teflon-like" coatings were achieved by tumbling the particles by playing AC/DC's song "Thunderstruck". The overcoating resulted in a markedly slower release of the cytotoxic drug, and this effect correlated positively with the plasma polymer coating times, ranging from 2-fold up to more than 100-fold. Ultimately, upon characterizing and verifying pSi MP production, loading, and coating with analytical methods such as time-of-flight secondary ion mass spectrometry, scanning electron microscopy, thermal gravimetry, water contact angle measurements, and fluorescence microscopy, human neuroblastoma cells were challenged with pSi MPs in an in vitro assay, revealing a significant time delay in cell death onset.

  17. Effective Viscosity in Porous Media and Applicable Limitations for Polymer Flooding of an Associative Polymer

    Directory of Open Access Journals (Sweden)

    Zhang Peng

    2015-11-01

    Full Text Available Hydrophobically associating polyacrylamide (HAPAM is considered to be a promising candidate for polymer flooding because of its excellent apparent viscosifying capability. Compared with partially hydrolyzed polyacrylamide (HPAM, the resistance factor and residual resistance factor caused by HAPAM tend to be higher. However, the effective viscosity of HAPAM is lower than that of conventional polymer at a concentration of 2 000 mg/L. The dynamic retention capacity of HAPAM is about 2.3 times that of HPAM. The oil displacement efficiency of HAPAM is lower than that of conventional polymer at a concentration of 2 000 mg/L in the homogeneous sandpack model. The oil displacement efficiency of HAPAM is higher than that of HPAM only in the heterogeneous model (permeability ratio 2.8. Neither high nor low permeability ratios are good for the oil displacement efficiency of HAPAM.

  18. Manufacture of porous biodegradable polymer conduits by an extrusion process for guided tissue regeneration

    Science.gov (United States)

    Widmer, M. S.; Gupta, P. K.; Lu, L.; Meszlenyi, R. K.; Evans, G. R.; Brandt, K.; Savel, T.; Gurlek, A.; Patrick, C. W. Jr; Mikos, A. G.; McIntire, L. V. (Principal Investigator)

    1998-01-01

    We have fabricated porous, biodegradable tubular conduits for guided tissue regeneration using a combined solvent casting and extrusion technique. The biodegradable polymers used in this study were poly(DL-lactic-co-glycolic acid) (PLGA) and poly(L-lactic acid) (PLLA). A polymer/salt composite was first prepared by a solvent casting process. After drying, the composite was extruded to form a tubular construct. The salt particles in the construct were then leached out leaving a conduit with an open-pore structure. PLGA was studied as a model polymer to analyze the effects of salt weight fraction, salt particle size, and processing temperature on porosity and pore size of the extruded conduits. The porosity and pore size were found to increase with increasing salt weight fraction. Increasing the salt particle size increased the pore diameter but did not affect the porosity. High extrusion temperatures decreased the pore diameter without altering the porosity. Greater decrease in molecular weight was observed for conduits manufactured at higher temperatures. The mechanical properties of both PLGA and PLLA conduits were tested after degradation in vitro for up to 8 weeks. The modulus and failure strength of PLLA conduits were approximately 10 times higher than those of PLGA conduits. Failure strain was similar for both conduits. After degradation for 8 weeks, the molecular weights of the PLGA and PLLA conduits decreased to 38% and 43% of the initial values, respectively. However, both conduits maintained their shape and did not collapse. The PLGA also remained amorphous throughout the time course, while the crystallinity of PLLA increased from 5.2% to 11.5%. The potential of seeding the conduits with cells for transplantation or with biodegradable polymer microparticles for drug delivery was also tested with dyed microspheres. These porous tubular structures hold great promise for the regeneration of tissues which require tubular scaffolds such as peripheral nerve

  19. A Novel Micro-porous Polymer Electrolyte Comprising SnO_2 Nanorods and P(MMA-AN)

    Institute of Scientific and Technical Information of China (English)

    P.Zhang; H.P.Zhang; Z.H.Li; Y.P.Wu

    2007-01-01

    1 Results Micro-porous polymer electrolytes(MPEs), which almost obtained by the conventional methods of phase inversion process or immersion precipitation method, have significant advantages such as high ionic conductivity and excellent mechanical properties[1].In our work, micro-porous structure is obtained by adding SnO2 nanorods usually used as gas senor materials into the polymer matrix, which proves a new way to prepare MPEs.SnO2 nanorods were synthesized by microemulsion hydrothermal method[2]. Th...

  20. Highly porous organic polymers bearing tertiary amine group and their exceptionally high CO2 uptake capacities

    Science.gov (United States)

    Gomes, Ruth; Bhaumik, Asim

    2015-02-01

    We report a very simple and unique strategy for synthesis of a tertiary amine functionalized high surface area porous organic polymer (POP) PDVTA-1 through the co-polymerization of monomers divinylbenzene (DVB) and triallylamine (TAA) under solvothermal reaction conditions. Two different PDVTA-1 samples have been synthesized by varying the molar ratio of the monomers. The porous polymeric materials have been thoroughly characterized by solid state 13C CP MAS-NMR, FT-IR and UV-vis spectroscopy, N2 sorption, HR TEM and FE SEM to understand its chemical environment, nanostructure, bonding, morphology and related surface properties. PDVTA-1 with higher amine content (DVB/TAA=4.0) showed exceptionally high CO2 uptake capacity of 85.8 wt% (19.5 mmol g-1) at 273 K and 43.69 wt% (9.93 mmol g-1) at 298 K under 3 bar pressure, whereas relatively low amine loaded material (DVB/TAA=7.0) shows uptake capacity of 59.2 wt% (13.45 mmol g-1) at 273 K and 34.36 wt% (7.81 mmol g-1) at 298 K. Highly porous nanostructure together with very high surface area and basicity at the surface due to the presence of abundant basic tertiary amine N-sites in the framework of PDVTA-1 could be responsible for very high CO2 adsorption.

  1. Large deformation ionic polymer-metal composites actuators based on porous Nafion membranes

    Science.gov (United States)

    Zhao, Dongxu; Li, Dichen; Wang, Yanjie; Luo, Meng; Chen, Hualing

    2016-04-01

    With advantages of low driving voltage, good flexibility and high electromechanical efficiency, ionic polymer-metal composites (IPMCs), which are one of the most attractive smart materials, have been research hotspot in actuators, sensors and artificial muscles. However, a serious drawback of little deformation of thick IPMC actuator limits its application. In this paper, we fabricated thick porous Nafion membranes by freeze-drying process. A series of Thermogravimetric analyses (TGA), Field emission scanning electron microscopy (FE-SEM) and Water uptake (WUP) tests were performed to examine the validity of the freeze-drying process and the pore size and the porosity. Then, the porous IPMCs were fabricated with the freeze-drying processed Nafion membranes by the solution casting and reducing plating. Finally, the IPMC actuators with the dimensions of 25× 5× 1 in millimeters were achieved and tested. The terminal deformation of the porous IPMC actuator increased by 739.7%, compared with the ordinary IPMC actuator with the same dimensions under the driving voltage of 2VDC.

  2. Vinyl Ester Oligomer Crosslinked Porous Polymers Prepared via Surfactant-Free High Internal Phase Emulsions

    Directory of Open Access Journals (Sweden)

    Yun Zhu

    2012-01-01

    Full Text Available Using vinyl ester resin (VER containing styrene (or methyl methacrylate and vinyl ester oligomer (VEO as external phase, Pickering high internal phase emulsions (Pickering HIPEs having internal phase volume fraction of up to 95 vol% were prepared with copolymer particles as sole stabilizer. Polymerizing the external phase of these Pickering HIPEs led to porous polymers (poly-Pickering-HIPEs. Compared to the polystyrene- (PS- based poly-Pickering-HIPEs which were prepared with mixture of styrene and divinylbenzene (DVB as crosslinker, the poly-Pickering-HIPEs herein showed much higher elastic modulus and toughness. The elastic modulus of these poly-Pickering-HIPEs increased with increasing the VEO concentration in the external phase, while it decreased with increasing internal phase volume fraction. Increasing VEO concentration in the external phase also resulted in a decrease in the average void diameter as well as a narrow void diameter distribution of the resulting poly-Pickering-HIPEs. In addition, there were many small pores in the voids surface caused by the volume contraction of VER during the polymerization, which suggests a new method to fabricate porous polymers having a well-defined hierarchical pore structure.

  3. Rational Design of Porous Conjugated Polymers and Roles of Residual Palladium for Photocatalytic Hydrogen Production.

    Science.gov (United States)

    Li, Lianwei; Cai, Zhengxu; Wu, Qinghe; Lo, Wai-Yip; Zhang, Na; Chen, Lin X; Yu, Luping

    2016-06-22

    Developing highly efficient photocatalyts for water splitting is one of the grand challenges in solar energy conversion. Here, we report the rational design and synthesis of porous conjugated polymer (PCP) that photocatalytically generates hydrogen from water splitting. The design mimics natural photosynthetics systems with conjugated polymer component to harvest photons and the transition metal part to facilitate catalytic activities. A series of PCPs have been synthesized with different light harvesting chromophores and transition metal binding bipyridyl (bpy) sites. The photocatalytic activity of these bpy-containing PCPs can be greatly enhanced due to the improved light absorption, better wettability, local ordering structure, and the improved charge separation process. The PCP made of strong and fully conjugated donor chromophore DBD (M4) shows the highest hydrogen production rate at ∼33 μmol/h. The results indicate that copolymerization between a strong electron donor and weak electron acceptor into the same polymer chain is a useful strategy for developing efficient photocatalysts. This study also reveals that the residual palladium in the PCP networks plays a key role for the catalytic performance. The hydrogen generation activity of PCP photocatalyst can be further enhanced to 164 μmol/h with an apparent quantum yield of 1.8% at 350 nm by loading 2 wt % of extra platinum cocatalyst.

  4. Thermomechanical analysis and durability of commercial micro-porous polymer Li-ion battery separators

    Science.gov (United States)

    Love, Corey T.

    2011-03-01

    Static and dynamic thermomechanical analysis was performed with a dynamic mechanical analyzer (DMA) to identify thermal and mechanical transitions for commercially available polymer separators under mechanical loading. Clear transitions in deformation mode were observed at elevated temperatures. These transitions identified the onset of separator "shutdown" which occurred at temperatures below the polymer melting point. Mechanical loading direction was critical to the overall integrity of the separator. Anisotropic separators (Celgard 2320, 2400 and 2500) were mechanically limited when pulled in tensile in the transverse direction. The anisotropy of these separators is a result of the dry technique used to manufacture the micro-porous membranes. Separators prepared using the wet technique (Entek Gold LP) behaved more uniformly, or biaxially, where all mechanical properties were nearly identical within the separator plane. The information provided by the DMA can also be useful for predicting the long-term durability of polymer separators in lithium-ion batteries exposed to electrolyte (solvent and salt), thermal fluctuations and electrochemical cycling. Small losses in mechanical integrity were observed for separators exposed to the various immersion environments over the 4-week immersion time.

  5. Microfluidic Fabrication of Porous Polymer Microspheres: Dual Reactions in Single Droplets

    KAUST Repository

    Gong, Xiuqing

    2009-06-16

    We report the microfluidic fabrication of macroporous polymer microspheres via the simultaneous reactions within single droplets, induced by LTV irradiation. The aqueous phase of the reaction is the decomposition of H 2O2 to yield oxygen, whereas the organic phase is the polymerization of NO A 61, ethylene glycol dimethacrylate (EGDMA), and tri (propylene glycol) diacrylate (TPGDA) precursors. We first used a liquid polymer precursor to encapsulate a multiple number of magnetic Fe3O 4 colloidal suspension (MCS) droplets in a core-shell structure, for the purpose of studying the number of such encapsulated droplets that can be reliably controlled through the variation of flow rates. It was found that the formation of one shell with one, two, three, or more encapsulated droplets is possible. Subsequently, the H2O2 solution was encapsulated in the same way, after which we investigated its decomposition under UV irradiation, which simultaneously induces the polymerization of the encapsulating shell. Because the H2O2 decomposition leads to the release of oxygen, porous microspheres were obtained from a combined H2O2 decomposition/polymer precursor polymerization reaction. The multiplicity of the initially encapsulated H2O 2 droplets ensures the homogeneous distribution of the pores. The pores inside the micrometer-sized spheres range from several micrometers to tens of micrometers, and the maximum internal void volume fraction can attain 70%, similar to that of high polymerized high internal phase emulsion (polyHIPE). © 2009 American Chemical Society.

  6. In vivo bone biocompatibility and degradation of porous fumarate-based polymer/alumoxane nanocomposites for bone tissue engineering.

    NARCIS (Netherlands)

    Mistry, A.S.; Pham, Q.P.; Schouten, C.; Yeh, T.; Christenson, E.M.; Mikos, A.G.; Jansen, J.A.

    2010-01-01

    The objective of this study was to determine how the incorporation of surface-modified alumoxane nanoparticles into a biodegradable fumarate-based polymer affects in vivo bone biocompatibility (characterized by direct bone contact and bone ingrowth) and in vivo degradability. Porous scaffolds were f

  7. Analysis of Void Growth and Coalescence in Porous Polymer Materials. Coalescence in Polymer Materials

    Directory of Open Access Journals (Sweden)

    S. A. Reffas

    2013-06-01

    Full Text Available The use of polymeric materials in engineering applications is growing more and more all over the world. This issue requests new methodologies of analysis in order to assess the material’s capability to withstand complex loads. The use of polyacetal in engineering applications has increased rapidly in the last decade. In order to evaluate the behavior, the damage and coalescence of this type of polymer, a numerical method based on damage which occurs following several stages (nucleation of cavities, their growth and coalescence in more advanced stages of deformation is proposed in this work. A particular attention is given on the stress-strain and the volumetric strain evolution under different triaxiality and for three initial void shapes. Its application to polyacetal allows approving this approach for technical polymers. Finally, this method allow us to compare the obtained results of basic calculations at different triaxiality and to discuss their possible influence on the initial size and the geometrical shape of the porosity on the material failure.

  8. Nanocrystalline porous TiO2 electrode with ionic liquid impregnated solid polymer electrolyte for dye sensitized solar cells.

    Science.gov (United States)

    Singh, Pramod K; Kim, Kang-Wook; Kim, Ki-Il; Park, Nam-Gyu; Rhee, Hee-Woo

    2008-10-01

    This communication reports the detailed fabrication of electrodes and solid polymer electrolyte with ionic liquid (IL) as an electrolyte for dye sensitized solar cell (DSSC). Thick porous TiO2 film has been obtained by spreading and sintering TiO2 colloidal paste using "doctor blade" and characterized by SEM, TEM and XRD. The polymer electrolyte was PEO:KI/I2 incorporated with 1-ethyl 3-methylimidazolium thiocyanate (EMImSCN) as IL. Dispersal of IL in the polymer electrolyte improved the ionic conductivity and cell efficiency.

  9. Porous polymers bearing functional quaternary ammonium salts as efficient solid catalysts for the fixation of CO2 into cyclic carbonates

    Science.gov (United States)

    Cai, Sheng; Zhu, Dongliang; Zou, Yan; Zhao, Jing

    2016-07-01

    A series of porous polymers bearing functional quaternary ammonium salts were solvothermally synthesized through the free radical copolymerization of divinylbenzene (DVB) and functionalized quaternary ammonium salts. The obtained polymers feature highly cross-linked matrices, large surface areas, and abundant halogen anions. These polymers were evaluated as heterogeneous catalysts for the synthesis of cyclic carbonates from epoxides and CO2 in the absence of co-catalysts and solvents. The results revealed that the synergistic effect between the functional hydroxyl groups and the halide anion Br- afforded excellent catalytic activity to cyclic carbonates. In addition, the catalyst can be easily recovered and reused for at least five cycles without significant loss in activity.

  10. Facile Carbonization of Microporous Organic Polymers into Hierarchically Porous Carbons Targeted for Effective CO2 Uptake at Low Pressures.

    Science.gov (United States)

    Gu, Shuai; He, Jianqiao; Zhu, Yunlong; Wang, Zhiqiang; Chen, Dongyang; Yu, Guipeng; Pan, Chunyue; Guan, Jianguo; Tao, Kai

    2016-07-20

    The advent of microporous organic polymers (MOPs) has delivered great potential in gas storage and separation (CCS). However, the presence of only micropores in these polymers often imposes diffusion limitations, which has resulted in the low utilization of MOPs in CCS. Herein, facile chemical activation of the single microporous organic polymers (MOPs) resulted in a series of hierarchically porous carbons with hierarchically meso-microporous structures and high CO2 uptake capacities at low pressures. The MOPs precursors (termed as MOP-7-10) with a simple narrow micropore structure obtained in this work possess moderate apparent BET surface areas ranging from 479 to 819 m(2) g(-1). By comparing different activating agents for the carbonization of these MOPs matrials, we found the optimized carbon matrials MOPs-C activated by KOH show unique hierarchically porous structures with a significant expansion of dominant pore size from micropores to mesopores, whereas their microporosity is also significantly improved, which was evidenced by a significant increase in the micropore volume (from 0.27 to 0.68 cm(3) g(-1)). This maybe related to the collapse and the structural rearrangement of the polymer farmeworks resulted from the activation of the activating agent KOH at high temperature. The as-made hierarchically porous carbons MOPs-C show an obvious increase in the BET surface area (from 819 to 1824 m(2) g(-1)). And the unique hierarchically porous structures of MOPs-C significantly contributed to the enhancement of the CO2 capture capacities, which are up to 214 mg g(-1) (at 273 K and 1 bar) and 52 mg g(-1) (at 273 K and 0.15 bar), superior to those of the most known MOPs and porous carbons. The high physicochemical stabilities and appropriate isosteric adsorption heats as well as high CO2/N2 ideal selectivities endow these hierarchically porous carbon materials great potential in gas sorption and separation.

  11. Sulfonate-grafted porous polymer networks for preferential CO2 adsorption at low pressure.

    Science.gov (United States)

    Lu, Weigang; Yuan, Daqiang; Sculley, Julian; Zhao, Dan; Krishna, Rajamani; Zhou, Hong-Cai

    2011-11-16

    A porous polymer network (PPN) grafted with sulfonic acid (PPN-6-SO(3)H) and its lithium salt (PPN-6-SO(3)Li) exhibit significant increases in isosteric heats of CO(2) adsorption and CO(2)-uptake capacities. IAST calculations using single-component-isotherm data and a 15/85 CO(2)/N(2) ratio at 295 K and 1 bar revealed that the sulfonate-grafted PPN-6 networks show exceptionally high adsorption selectivity for CO(2) over N(2) (155 and 414 for PPN-6-SO(3)H and PPN-6-SO(3)Li, respectively). Since these PPNs also possess ultrahigh physicochemical stability, practical applications in postcombustion capture of CO(2) lie well within the realm of possibility.

  12. Poly-functional porous-organic polymers to access functionality – CO 2 sorption energetic relationships

    KAUST Repository

    Alkordi, Mohamed H.

    2015-09-21

    Herein, we report a facile approach towards the construction of poly-functional porous organic polymers (POPs). The functional groups employed were selected to span the range of Lewis-base to neutral to Lewis-acid character. Our results underline the effect of chemical functionality on the observed Q for CO adsorption inside the material, being largest for functional groups with electron donating O- and N-centered Lewis base sites. Our systematic investigation within a family of POPs revealed a wide range for CO heat of adsorption (23.8-53.8 kJ mol) that is clearly associated with the chemical nature of the functional groups present. In addition, post-synthetic modification of POPs reported herein demonstrated a facile pathway to dramatically enhance carbon dioxide uptake energetics.

  13. Preparation of Carbon Nanotubes by the Catalysis of Polymer Metal Complex on Porous Al203 Matrix

    Institute of Scientific and Technical Information of China (English)

    SHI YanLi; ZHANG XiaoGang; LI HuLin

    2001-01-01

    @@ At present, synthesis of carbon nanotubes (CNTs) is normally conducted on a vapor-to-solid interface at ca. 500-3500℃ via various vapor phase methods, such as are discharge, laser ablation, catalytic pyrolysis and chemical vapor deposition, etc.1-2 Recently, channel materials (such as channels of alumina and of AlPO4-5 zeolite) 3 have been utilized as solid-state templates to grow CNTs inside the channel. Here we described a novel method to prepare the carbon nanotubes based on the decomposition of C2H2 gas on the Co-Ni catalyst anchored by polymer complex on the porous A12O3 matrix. The degree of graphitization of synthesized CNTs and catalysts are of great interest.

  14. Preparation of Carbon Nanotubes by the Catalysis of Polymer Metal Complex on Porous Al203 Matrix

    Institute of Scientific and Technical Information of China (English)

    SHI; YanLi

    2001-01-01

    At present, synthesis of carbon nanotubes (CNTs) is normally conducted on a vapor-to-solid interface at ca. 500-3500℃ via various vapor phase methods, such as are discharge, laser ablation, catalytic pyrolysis and chemical vapor deposition, etc.1-2 Recently, channel materials (such as channels of alumina and of AlPO4-5 zeolite) 3 have been utilized as solid-state templates to grow CNTs inside the channel. Here we described a novel method to prepare the carbon nanotubes based on the decomposition of C2H2 gas on the Co-Ni catalyst anchored by polymer complex on the porous A12O3 matrix. The degree of graphitization of synthesized CNTs and catalysts are of great interest.  ……

  15. Synthesis of Nanoscale Lithium-Ion Battery Cathode Materials Using a Porous Polymer Precursor Method

    KAUST Repository

    Deshazer, H.D.

    2011-01-01

    Fine particles of metal oxides with carefully controlled compositions can be easily prepared by the thermal decomposition of porous polymers, such as cellulose, into which solutions containing salts of the desired cations have been dissolved. This is a simple and versatile method that can be used to produce a wide variety of materials with a range of particle sizes and carefully controlled chemical compositions. Examples of the use of this method to produce fine particles of LiCoO2 and Li(NiMnCo)1/3O2, which are used in the positive electrodes of lithium-ion batteries, are shown. Experiments have demonstrated that materials made using this method can have electrochemical properties comparable to those typically produced by more elaborate procedures. © 2011 The Electrochemical Society.

  16. Nanospace-Mediated Self-Organization of Nanoparticles in Flexible Porous Polymer Templates.

    Science.gov (United States)

    Kuroda, Yoshiyuki; Muto, Itaru; Shimojima, Atsushi; Wada, Hiroaki; Kuroda, Kazuyuki

    2017-08-31

    Self-organization is a fundamental process for the construction of complex hierarchically ordered nanostructures, which are widespread in biological systems. However, precise control of size, shape, and surface properties is required for self-organization of nanoparticles. Here, we demonstrate a novel self-organization phenomenon mediated by flexible nanospaces in templates. Inorganic nanoparticles (e.g., silica, zirconia, and titania) are deposited in porous polymer thin films with randomly distributed pores on the surface, leaving a partially filled nanospace in each pore. Heating at temperatures beyond the glass transition temperature of the template leads to self-organization of the inorganic nanoparticles into one-dimensional chainlike networks. The self-organization is mediated by the deformation and fusion of the residual nanospaces, and it can be rationally controlled by sequential heat treatments. These results show that a nanospace, defined by the nonexistence of matter, interacts indirectly with matter and can be used as a component of self-organization systems.

  17. Measurement of creatinine in human plasma using a functional porous polymer structure sensing motif.

    Science.gov (United States)

    Nanda, Sitansu Sekhar; An, Seong Soo A; Yi, Dong Kee

    2015-01-01

    In this study, a new method for detecting creatinine was developed. This novel sensor comprised of two ionic liquids, poly-lactic-co-glycolic acid (PLGA) and 1-butyl-3-methylimidazolium (BMIM) chloride, in the presence of 2',7'-dichlorofluorescein diacetate (DCFH-DA). PLGA and BMIM chloride formed a functional porous polymer structure (FPPS)-like structure. Creatinine within the FPPS rapidly hydrolyzed and released OH(-), which in turn converted DCFH-DA to DCFH, developing an intense green color or green fluorescence. The conversion of DCFH to DCF(+) resulted in swelling of FPPS and increased solubility. This DCF(+)-based sensor could detect creatinine levels with detection limit of 5 µM and also measure the creatinine in blood. This novel method could be used in diagnostic applications for monitoring individuals with renal dysfunction.

  18. Singlet oxygen generation using a porous monolithic polymer supported photosensitizer: potential application to the photodynamic destruction of melanoma cells.

    Science.gov (United States)

    Burguete, M Isabel; Galindo, Francisco; Gavara, Raquel; Luis, Santiago V; Moreno, Miguel; Thomas, Paul; Russell, David A

    2009-01-01

    Photogeneration of singlet oxygen (1O2) by rose bengal is improved through the use of a porous monolithic polymer (PMP) as a support, as compared to a classic gel-type resin matrix. This type of monolithic polymeric matrix can be made at a multigram scale in quantitative yields enabling the preparation of large amounts of supported photosensitizer at low cost. The singlet oxygen induced oxidation of 9,10-diphenylanthracene has been used as a benchmark reaction, and a comparative study using rose bengal in solution, entrapped within gel-type derived polymer and entrapped within a porous monolithic polymer (PMP) has been performed. The enhanced photoreactivity of the PMP-rose bengal conjugates has been utilised for the successful photodynamic therapy (PDT) of melanoma cells.

  19. In-syringe extraction using dissolvable layered double hydroxide-polymer sponges templated from hierarchically porous coordination polymers.

    Science.gov (United States)

    Ghani, Milad; Frizzarin, Rejane M; Maya, Fernando; Cerdà, Víctor

    2016-07-01

    Herein we report the use of cobalt porous coordination polymers (PCP) as intermediates to prepare advanced extraction media based on layered double hydroxides (LDH) supported on melamine polymer foam. The obtained dissolvable Ni-Co LDH composite sponges can be molded and used as sorbent for the in-syringe solid-phase extraction (SPE) of phenolic acids from fruit juices. The proposed sorbent is obtained due to the surfactant-assisted self-assembly of Co(II)/imidazolate PCPs on commercially available melamine foam, followed by the in situ conversion of the PCP into the final dissolvable LDH coating. Advantageous features for SPE are obtained by using PCPs with hierarchical porosity (HPCPs). The LDH-sponge prepared using intermediate HPCPs (HLDH-sponge) is placed in the headspace of a glass syringe, enabling flow-through extraction followed by analyte elution by the dissolution of the LDH coating in acidic conditions. Three phenolic acids (gallic acid, p-hydroxybenzoic acid and caffeic acid) were extracted and quantified using high performance liquid chromatography. Using a 5mL sample volume, the obtained detection limits were 0.15-0.35μgL(-1). The proposed method for the preparation of HLDH-sponges showed a good reproducibility as observed from the intra- and inter-day RSD's, which were <10% for all analytes. The batch-to-batch reproducibility for three different batches of HLDH-sponges was 10.6-11.2%. Enrichment factors of 15-21 were obtained. The HLDH-sponges were applied satisfactorily to the determination of phenolic acids in natural and commercial fruit juices, obtaining relative recoveries among 89.7-95.3%.

  20. Phospholipid arrays on porous polymer coatings generated by micro-contact spotting

    Directory of Open Access Journals (Sweden)

    Sylwia Sekula-Neuner

    2017-03-01

    Full Text Available Nanoporous poly(2-hydroxyethyl methacrylate-co-ethylene dimethacrylate (HEMA-EDMA is used as a 3D mesh for spotting lipid arrays. Its porous structure is an ideal matrix for lipid ink to infiltrate, resulting in higher fluorescent signal intensity as compared to similar arrays on strictly 2D substrates like glass. The embedded lipid arrays show high stability against washing steps, while still being accessible for protein and antibody binding. To characterize binding to polymer-embedded lipids we have applied Streptavidin as well as biologically important biotinylated androgen receptor binding onto 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-(cap biotinyl (Biotinyl Cap PE and anti-DNP IgE recognition of 2,4-dinitrophenyl[1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-[6-[(2,4-dinitrophenylamino]hexanoyl] (DNP] antigen. This approach adds lipid arrays to the range of HEMA polymer applications and makes this solid substrate a very attractive platform for a variety of bio-applications.

  1. Superficially porous particles with 1000Å pores for large biomolecule high performance liquid chromatography and polymer size exclusion chromatography.

    Science.gov (United States)

    Wagner, Brian M; Schuster, Stephanie A; Boyes, Barry E; Shields, Taylor J; Miles, William L; Haynes, Mark J; Moran, Robert E; Kirkland, Joseph J; Schure, Mark R

    2017-03-17

    To facilitate mass transport and column efficiency, solutes must have free access to particle pores to facilitate interactions with the stationary phase. To ensure this feature, particles should be used for HPLC separations which have pores sufficiently large to accommodate the solute without restricted diffusion. This paper describes the design and properties of superficially porous (also called Fused-Core(®), core shell or porous shell) particles with very large (1000Å) pores specifically developed for separating very large biomolecules and polymers. Separations of DNA fragments, monoclonal antibodies, large proteins and large polystyrene standards are used to illustrate the utility of these particles for efficient, high-resolution applications.

  2. Augmented cellular trafficking and endosomal escape of porous silicon nanoparticles via zwitterionic bilayer polymer surface engineering.

    Science.gov (United States)

    Shahbazi, Mohammad-Ali; Almeida, Patrick V; Mäkilä, Ermei M; Kaasalainen, Martti H; Salonen, Jarno J; Hirvonen, Jouni T; Santos, Hélder A

    2014-08-01

    The development of a stable vehicle with low toxicity, high cellular internalization, efficient endosomal escape, and optimal drug release profile is a key bottleneck in nanomedicine. To overcome all these problems, we have developed a successful layer-by-layer method to covalently conjugate polyethyleneimine (PEI) and poly(methyl vinyl ether-co-maleic acid) (PMVE-MA) copolymer on the surface of undecylenic acid functionalized thermally hydrocarbonized porous silicon nanoparticles (UnTHCPSi NPs), forming a bilayer zwitterionic nanocomposite containing free positive charge groups of hyper-branched PEI disguised by the PMVE-MA polymer. The surface smoothness, charge and hydrophilicity of the developed NPs considerably improved the colloidal and plasma stabilities via enhanced suspensibility and charge repulsion. Furthermore, despite the surface negative charge of the bilayer polymer-conjugated NPs, the cellular trafficking and endosomal escape were significantly increased in both MDA-MB-231 and MCF-7 breast cancer cells. Remarkably, we also showed that the conjugation of surface free amine groups of the highly toxic UnTHCPSi-PEI (Un-P) NPs to the carboxylic groups of PMVE-MA renders acceptable safety features to the system and preserves the endosomal escape properties via proton sponge mechanism of the free available amine groups located inside the hyper-branched PEI layer. Moreover, the double layer protection not only controlled the aggregation of the NPs and reduced the toxicity, but also sustained the drug release of an anticancer drug, methotrexate, with further improved cytotoxicity profile of the drug-loaded particles. These results provide a proof-of-concept evidence that such zwitterionic polymer-based PSi nanocomposites can be extensively used as a promising candidate for cytosolic drug delivery.

  3. Efficacy and safety of a novel nano-porous polymer-free sirolimuseluting stent in pigs

    Institute of Scientific and Technical Information of China (English)

    CHEN Ming; ZHENG Bo; WU Zheng; PENG Hong-yu; WANG Xin-gang; ZHANG bin; HUO Yong

    2013-01-01

    Background Drug-eluting stents represent a major advance in interventional cardiology.However,the current drugeluting stents have significant limitations.One of the major problems is very late stent thrombosis,which is likely caused by inflammation and a hypersensitivity reaction related to a polymer on the stent.A polymer-free sirolimus-eluting stent with a unique nano-porous surface has been developed.This study aimed to evaluate this novel polymer-free sirolimuseluting stent for its efficacy and safety in a pig model.Methods Stents were directly coated with sirolimus (a drug concentration of 2.2 μg/mm2 on the stent surface).The polymer-free sirolimus-eluting stents (PFSES) were compared to standard polymer-coated sirolimus-eluting stents (PCSES) and bare-metal stents (BMS) in 18 pigs.Results At one month the degree of neointimal hyperplasia was similar between the two sirolimus-eluting stent groups and was significantly less compared to BMS ((1.93±0.51) mm2,(1.57±0.69) mm2 vs.(4.45±1.05) mm2,P <0.05) At three months,PFSES maintained the low level of neointima ((2.41±0.99) mm2 vs.(4.32±1.16) mm2,P <0.05),whereas PCSES had developed significant neointimal proliferation similar to BMS.The inflammation level was significantly higher in PCSES when compared with BMS three months post-implantation (2.50±0.55 vs.0.83±0.75,P <0.05) whereas PFSES showed a low level of inflammation comparable to PCSES (1.33±0.52 vs.2.50±0.55,P <0.05).Conclusion The PFSES is effective and safe,and appears to be superior to standard PCSEs.

  4. Infiltration Behaviour of Polymer-Modified Porous Concrete and Porous Asphalt Surfaces Used in SuDS Techniques

    OpenAIRE

    Sañudo Fontaneda, Luis Ángel; Rodríguez Hernández, Jorge; Calzada Pérez, Miguel Ángel; Castro Fresno, Daniel

    2014-01-01

    Permeable pavements are one of the world’s most widely applied techniques for source control in sustainable drainage systems. Porous concrete (PC) and porous asphalt (PA) are two of the most studied surfaces in terms of runoff reduction. Nevertheless, previous research has highlighted a lack of a comprehensive laboratory methodology for the analysis of the topographical variables, runoff surface length (RSL) and surface slope (SS), and their impact on the infiltration behaviour of these porou...

  5. Surface-Localized Sealing of Porous Ultralow-k Dielectric Films with Ultrathin (<2 nm) Polymer Coating.

    Science.gov (United States)

    Yoon, Seong Jun; Pak, Kwanyong; Nam, Taewook; Yoon, Alexander; Kim, Hyungjun; Im, Sung Gap; Cho, Byung Jin

    2017-08-22

    Semiconductor integrated circuit chip industries have been striving to introduce porous ultralow-k (ULK) dielectrics into the multilevel interconnection process in order to improve their chip operation speed by reducing capacitance along the signal path. To date, however, highly porous ULK dielectrics (porosity >40%, dielectric constant (k) <2.4) have not been successfully adopted in real devices because the porous nature causes many serious problems, including noncontinuous barrier deposition, penetration of the barrier metal, and reliability issues. Here, a method that allows porous ULK dielectrics to be successfully used with a multilevel interconnection scheme is presented. The surface of the porous ULK dielectric film (k = 2.0, porosity ∼47%) could be completely sealed by a thin (<2 nm) polymer deposited by a multistep initiated chemical vapor deposition (iCVD) process. Using the iCVD process, a thin pore-sealing layer was localized only to the surface of the porous ULK dielectric film, which could minimize the increase of k; the final effective k was less than 2.2, and the penetration of metal barrier precursors into the dielectric film was completely blocked. The pore-sealed ULK dielectric film also exhibited excellent long-term reliability comparable to a dense low-k dielectric film.

  6. Porous organic polymers with anchored aldehydes: A new platform for post-synthetic amine functionalization en route for enhanced CO2 adsorption properties

    KAUST Repository

    Guillerm, Vincent

    2014-01-01

    A novel porous organic polymer has been synthesized using the molecular building block approach to deliberately encompass aldehyde functionalities amenable to post functionalization. The resultant porous framework allows a facile, one-step quantitative and post-synthetic functionalization by amines, permitting enhanced CO2 sorption properties. © 2014 The Royal Society of Chemistry.

  7. Biodegradable polymer for sealing porous PEO layer on pure magnesium: An in vitro degradation study

    Energy Technology Data Exchange (ETDEWEB)

    Alabbasi, Alyaa; Mehjabeen, Afrin [Biomaterials and Engineering Materials (BEM) Laboratory, James Cook University, Townsville 4811, Queensland (Australia); Kannan, M. Bobby, E-mail: bobby.mathan@jcu.edu.au [Biomaterials and Engineering Materials (BEM) Laboratory, James Cook University, Townsville 4811, Queensland (Australia); Ye, Qingsong [Discipline of Dentistry, James Cook University, Townsville 4811, Queensland (Australia); Blawert, Carsten [Magnesium Innovation Centre, Institute of Materials Research, Helmholtz-Zentrum Geesthacht, Geesthacht 21502 (Germany)

    2014-05-01

    Graphical abstract: - Highlights: • Poly(L-lactide) was used to seal the porous PEO layer on Mg. • The dual-layer coating improved the in vitro degradation resistance of Mg. • Localized degradation was inhibited in the dual-layer coated Mg. - Abstract: An attempt was made to seal the porous silicate-based plasma electrolytic oxidation (PEO) layer on pure magnesium (Mg) with a biodegradable polymer, poly(L-lactide) (PLLA), to delay the localized degradation of magnesium-based implants in body fluid for better in-service mechanical integrity. Firstly, a silicate-based PEO coating on pure magnesium was performed using a pulsed constant current method. In order to seal the pores in the PEO layer, PLLA was coated using a two-step spin coating method. The performance of the PEO–PLLA Mg was evaluated using electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization. The EIS results showed that the polarization resistance (R{sub p}) of the PEO–PLLA Mg was close to two orders of magnitude higher than that of the PEO Mg. While the corrosion current density (i{sub corr}) of the pure Mg was reduced by 65% with the PEO coating, the PEO–PLLA coating reduced the i{sub corr} by almost 100%. As expected, the R{sub p} of the PEO–PLLA Mg decreased with increase in exposure time. However, it was noted that the R{sub p} of the PEO–PLLA Mg even after 100 h was six times higher than that of the PEO Mg after 48 h exposure, and did not show any visible localized attack.

  8. Periodic porous stripe patterning in a polymer blend film induced by phase separation during spin-casting.

    Science.gov (United States)

    Kim, Jae-Kyung; Taki, Kentaro; Nagamine, Shinsuke; Ohshima, Masahiro

    2008-08-19

    A periodic striping pattern with microscale pore size is observed on the surface of thin films prepared by spin-casting from a polystyrene (PS) and polyethylene glycol (PEG) blend solution. The pattern is created by the convection generated by thermal gradients in the solution between the substrate and film solution during solvent evaporation, the radial flow of the spin-coated solution, and the primary and secondary phase separation of the PS and PEG solutions. The formation mechanism of the periodic porous stripe pattern is discussed, wherein the effects of the polymer blend weight ratio, polymer concentration, and drying rate on the formation of the periodic porous striping pattern are investigated using scanning electron and atomic force microscopy.

  9. Post-Synthesis Functionalization of Porous Organic Polymers for CO2 Capture

    KAUST Repository

    Al Otaibi, Mona S.

    2014-07-01

    Solid porous materials are network materials that contain space void. Porous Organic Polymers (POPs) are porous materials, which are constructed from organic building blocks and exhibit large surface area with low densities. Due to these characteristics, POPs have attracted attentions because of their potential use in application such as gas storage and chemical separation. This thesis presents a study of the synthesis of novel POP being a network based on 2,5- dibromobenzaldehyde and 1,3,5-triethynylbenzene linked together via Sonogashira- Hagihara (SH) coupling. This network showed a relatively good surface area of 770 m2/g and total pore volume of 0.59 cc/g. In addition, it proved to be chemically and thermally stable, maintaining the thermal stability up to 350oC. In addition to synthesize novel aldehyde-POP network, it was also possible to post synthetically modify a network via one-step post synthetic functionalization by amine. Ethelynediamine (EDA), Diethylenetriamine (DETA), and Tris(2-aminoethyl)amine (Tris-amine) are three different amines used for aldehyde-POP functionalization. The produced networks were aminated via different amine species substitution the aldehyde group present within the network. Modification to these networks resulted in a decrease in surface area from 770 m2.g-1 to 333 m2.g-1, 162 m2.g-1, and 211 m2.g-1 in respective to EDA, DETA, and Tris-amine. Although the surface areas were decreased, the CO2 adsorption was enhanced as evidenced by the increase of Qst (i.e., from 25 to 45 kJ.mol-1 for DETA at low coverage). Our findings are expected to strengthen existing research areas of the influence of different type of amines (e.g aromatic amine) on CO2 adsorption. Although amine grafting has been studied in other systems (e.g., PAFs and MOFs), we are the first to reported amine functionalized POPs using a novel one-step amine grafting PSM procedure. Future research might extend to study the interaction between CO2 and amine species under

  10. Fabrication of interfacial functionalized porous polymer monolith and its adsorption properties of copper ions.

    Science.gov (United States)

    Han, Jiaxi; Du, Zhongjie; Zou, Wei; Li, Hangquan; Zhang, Chen

    2014-07-15

    The interfacial functionalized poly (glycidyl methacrylate) (PGMA) porous monolith was fabricated and applied as a novel porous adsorbent for copper ions (Cu(2+)). PGMA porous material with highly interconnected pore network was prepared by concentrated emulsion polymerization template. Then polyacrylic acid (PAA) was grafted onto the interface of the porous monolith by the reaction between the epoxy group on PGMA and a carboxyl group on PAA. Finally, the porous monolith was interfacial functionalized by rich amount of carboxyl groups and could adsorb copper ions effectively. The chemical structure and porous morphology of the porous monolith were measured by Fourier transform infrared spectroscopy and scanning electron microscopy. Moreover, the effects of pore size distribution, pH value, co-existing ions, contacting time, and initial concentrations of copper ions on the adsorption capacity of the porous adsorbents were studied.

  11. Synthesis of porous molecularly imprinted polymers for selective adsorption of glutathione

    Science.gov (United States)

    Song, Renyuan; Hu, Xiaoling; Guan, Ping; Li, Ji; Qian, Liwei; Wang, Chaoli; Wang, Qiaoli

    2015-03-01

    An effective approach overcome the classical deficiencies of biomolecules molecularly imprinted polymers (MIPs), that is, low binding capacity and slow mass transfer rate, is proposed. With glutathione (GSH) as target molecule, porous imprinted layers were fabricated according to our newly developed method the introduction of a mixture of acetontrile and dimethylsulfoxide as porogen in surface-initiated polymerization systems. The resultant MIPs particles exhibited a large surface area could remarkably improve the imprinting effect in relation to a significantly increased imprinting factor and mass transfer rate, compared to the MIPs prepared by using aqueous solution as solvent. The batch static binding tests were carried out to evaluate the adsorption kinetics, adsorption isotherms and selective recognition of the MIPs particles. The binding behavior followed the pseudo-second order kinetic model, revealing that the process was chemically carried out. Two binding isotherm models were applied to analyze equilibrium data, obtaining the best description by Langmuir isotherm model. In addition, the selective of separation and extraction of GSH from a mixture of GSH and its structural analogs could be achieved on the MIPs solid-phase extraction cartridge, indicating that the possibility for the separation and enrichment of the template from complicated matrices.

  12. Viscoelastic polymer flows and elastic turbulence in three-dimensional porous structures.

    Science.gov (United States)

    Mitchell, Jonathan; Lyons, Kyle; Howe, Andrew M; Clarke, Andrew

    2016-01-14

    Viscoelastic polymer solutions flowing through reservoir rocks have been found to improve oil displacement efficiency when the aqueous-phase shear-rate exceeds a critical value. A possible mechanism for this enhanced recovery is elastic turbulence that causes breakup and mobilization of trapped oil ganglia. Here, we apply nuclear magnetic resonance (NMR) pulsed field gradient (PFG) diffusion measurements in a novel way to detect increased motion of disconnected oil ganglia. The data are acquired directly from a three-dimensional (3D) opaque porous structure (sandstone) when viscoelastic fluctuations are expected to be present in the continuous phase. The measured increase in motion of trapped ganglia provides unequivocal evidence of fluctuations in the flowing phase in a fully complex 3D system. This work provides direct evidence of elastic turbulence in a realistic reservoir rock - a measurement that cannot be readily achieved by conventional laboratory methods. We support the NMR data with optical microscopy studies of fluctuating ganglia in simple two-dimensional (2D) microfluidic networks, with consistent apparent rheological behaviour of the aqueous phase, to provide conclusive evidence of elastic turbulence in the 3D structure and hence validate the proposed flow-fluctuation mechanism for enhanced oil recovery.

  13. Preparation of porous polymer monoliths featuring enhanced surface coverage with gold nanoparticles

    KAUST Repository

    Lv, Yongqin

    2012-10-01

    A new approach to the preparation of porous polymer monoliths with enhanced coverage of pore surface with gold nanoparticles has been developed. First, a generic poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith was reacted with cystamine followed by the cleavage of its disulfide bonds with tris(2-carboxylethyl)phosphine, which liberated the desired thiol groups. Dispersions of gold nanoparticles with sizes varying from 5 to 40. nm were then pumped through the functionalized monoliths. The materials were then analyzed using both energy dispersive X-ray spectroscopy and thermogravimetric analysis. We found that the quantity of attached gold was dependent on the size of nanoparticles, with the maximum attachment of more than 60. wt% being achieved with 40. nm nanoparticles. Scanning electron micrographs of the cross sections of all the monoliths revealed the formation of a non-aggregated, homogenous monolayer of nanoparticles. The surface of the bound gold was functionalized with 1-octanethiol and 1-octadecanethiol, and these monolithic columns were used successfully for the separations of proteins in reversed phase mode. The best separations were obtained using monoliths modified with 15, 20, and 30. nm nanoparticles since these sizes produced the most dense coverage of pore surface with gold. © 2012 Elsevier B.V.

  14. Highly Stable and Porous Cross-Linked Polymers for Efficient Photocatalysis

    Energy Technology Data Exchange (ETDEWEB)

    Xie, Zhigang; Wang, Cheng; deKrafft, Kathryn E.; Lin, Wenbin

    2011-02-23

    Porous cross-linked polymers (PCPs) with phosphorescent [Ru(bpy)₃]{sup 2+} and [Ir(ppy)₂(bpy)]{sup +} building blocks were obtained via octacarbonyldicobalt (Co₂(CO)₈)-catalyzed alkyne trimerization reactions. The resultant Ru- and Ir-PCPs exhibited high porosity with specific surface areas of 1348 and 1547 m²/g, respectively. They are thermally stable at up to 350 °C in air and do not dissolve or decompose in all solvents tested, including concentrated hydrochloric acid. The photoactive PCPs were shown to be highly effective, recyclable, and reusable heterogeneous photocatalysts for aza-Henry reactions, α-arylation of bromomalonate, and oxyamination of an aldehyde, with catalytic activities comparable to those of the homogeneous [Ru(bpy)₃]{sup 2+} and [Ir(ppy)₂(bpy)]{sup +} photocatalysts. This work highlights the potential of developing photoactive PCPs as highly stable, molecularly tunable, and recyclable and reusable heterogeneous photocatalysts for a variety of important organic transformations.

  15. Highly porous polymer-derived wollastonite-hydroxycarbonate apatite ceramics for bone regeneration.

    Science.gov (United States)

    Fiocco, L; Li, S; Bernardo, E; Stevens, M M; Jones, J R

    2016-04-12

    A novel strategy was employed to synthesize highly porous wollastonite-hydroxycarbonate apatite ceramic scaffolds for bone regeneration. A commercial liquid preceramic polymer filled with micro-CaCO3 powders was foamed at low temperature (at 350 °C), using the decomposition of a hydrazine additive, and then converted into ceramic by a treatment at 700 °C. Hydroxycarbonate apatite was later developed by a phosphatization treatment of ceramized foams, in a P-rich solution, while wollastonite was obtained by a second firing, at 900 °C. The effectiveness of the method was proven by x-ray diffraction analysis, showing the presence of the two expected crystalline phases. Porosity, interconnect size distribution and mechanical strength were in the range that is thought to be suitable for bone regeneration in non-load bearing sites (compressive strength ≈ 3 MPa, porosity ≈ 90%, modal interconnect diameter ≈ 130-160 μm). In addition, bioactivity and ion release rate were assessed in simulated body fluid (SBF). MC3T3 osteoblast precursor cells were able to colonize the material in vitro through the pore architecture and expressed osteogenic markers.

  16. Natural gas purification using a porous coordination polymer with water and chemical stability.

    Science.gov (United States)

    Duan, Jingui; Jin, Wanqin; Krishna, Rajamani

    2015-05-04

    Porous coordination polymers (PCPs), constructed by bridging the metals or clusters and organic linkers, can provide a functional pore environment for gas storage and separation. But the rational design for identifying PCPs with high efficiency and low energy cost remains a challenge. Here, we demonstrate a new PCP, [(Cu4Cl)(BTBA)8·(CH3)2NH2)·(H2O)12]·xGuest (PCP-33⊃guest), which shows high potential for purification of natural gas, separation of C2H2/CO2 mixtures, and selective removal of C2H2 from C2H2/C2H4 mixtures at ambient temperature. The lower binding energy of the framework toward these light hydrocarbons indicates the reduced net costs for material regeneration, and meanwhile, the good water and chemical stability of it, in particular at pH = 2 and 60 °C, shows high potential usage under some harsh conditions. In addition, the adsorption process and effective site for separation was unravelled by in situ infrared spectroscopy studies.

  17. Biodegradable polymer for sealing porous PEO layer on pure magnesium: An in vitro degradation study

    Science.gov (United States)

    Alabbasi, Alyaa; Mehjabeen, Afrin; Kannan, M. Bobby; Ye, Qingsong; Blawert, Carsten

    2014-05-01

    An attempt was made to seal the porous silicate-based plasma electrolytic oxidation (PEO) layer on pure magnesium (Mg) with a biodegradable polymer, poly(L-lactide) (PLLA), to delay the localized degradation of magnesium-based implants in body fluid for better in-service mechanical integrity. Firstly, a silicate-based PEO coating on pure magnesium was performed using a pulsed constant current method. In order to seal the pores in the PEO layer, PLLA was coated using a two-step spin coating method. The performance of the PEO-PLLA Mg was evaluated using electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization. The EIS results showed that the polarization resistance (Rp) of the PEO-PLLA Mg was close to two orders of magnitude higher than that of the PEO Mg. While the corrosion current density (icorr) of the pure Mg was reduced by 65% with the PEO coating, the PEO-PLLA coating reduced the icorr by almost 100%. As expected, the Rp of the PEO-PLLA Mg decreased with increase in exposure time. However, it was noted that the Rp of the PEO-PLLA Mg even after 100 h was six times higher than that of the PEO Mg after 48 h exposure, and did not show any visible localized attack.

  18. Selective, ultrathin membrane skins prepared by deposition of novel polymer films on porous alumina supports

    Science.gov (United States)

    Balachandra, Anagi Manjula

    Membrane-based separations are attractive in industrial processes because of their low energy costs and simple operation. However, low permeabilities often make membrane processes uneconomical. Since flux is inversely proportional to membrane thickness, composite membranes consisting of ultrathin, selective skins on highly permeable supports are required to simultaneously achieve high throughput and high selectivity. However, the synthesis of defect-free skins with thicknesses less than 50 nm is difficult, and thus flux is often limited. Layer-by-layer deposition of oppositely charged polyelectrolytes on porous supports is an attractive method to synthesize ultrathin ion-separation membranes with high flux and high selectivity. The ion-transport selectivity of multilayer polyelectrolyte membranes (MPMs) is primarily due to Donnan exclusion; therefore increase in fixed charge density should yield high selectivity. However, control over charge density in MPMs is difficult because charges on polycations are electrostatically compensated by charges on polyanions, and the net charge in the bulk of these films is small. To overcome this problem, we introduced a templating method to create ion-exchange sites in the bulk of the membrane. This strategy involves alternating deposition of a Cu2+-poly(acrylic acid) complex and poly(allylamine hydrochloride) on a porous alumina support followed by removal of Cu2+ and deprotonation to yield free -COO- ion-exchange sites. Diffusion dialysis studies showed that the Cl-/SO42-. Selectivity of Cu2+-templated membranes is 4-fold higher than that of membranes prepared in the absence of Cu2+. Post-deposition cross-linking of these membranes by heat-induced amide bond formation further increased Cl-/SO42- selectivity to values as high as 600. Room-temperature, surface-initiated atom transfer radical polymerization (ATRP) provides another convenient method for formation of ultrathin polymer skins. This process involves attachment of

  19. Preparation of porous, chemically cross-linked, PVdF-based gel polymer electrolytes for rechargeable lithium batteries

    Science.gov (United States)

    Cheng, C. L.; Wan, C. C.; Wang, Y. Y.

    This study reports the development of a new system of porous, chemically cross-linked, gel polymer electrolytes based on poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) copolymer as a polymer matrix, polyethylene glycol (PEG) as a plasticizer, and polyethylene glycol dimethacrylate (PEGDMA) as a chemical cross-linking oligomer. The electrolytes are prepared by a combination of controlled evaporation and thermal polymerization of PEGDMA. PVdF-HFP/PEG/PEGDMA gel polymer electrolytes with a composition of 5/3/2 exhibit both high ambient ionic conductivity, viz., >1 mS cm -1, and a high tensile modulus of 52 MPa, because of their porous and network structures. All the blends of electrolytes are electrochemically stable up to 5 V versus Li/Li + in the presence of 1 M LiPF 6/ethylene carbonate-diethyl carbonate (EC-DEC). With these polymer electrolytes, rechargeable lithium batteries composed of carbon anode and LiCoO 2 cathode have acceptable cycleability and a good rate capability.

  20. Fabrication of interfacial functionalized porous polymer monolith and its adsorption properties of copper ions

    Energy Technology Data Exchange (ETDEWEB)

    Han, Jiaxi; Du, Zhongjie; Zou, Wei; Li, Hangquan; Zhang, Chen, E-mail: zhangch@mail.buct.edu.cn

    2014-07-15

    Highlights: • Interface functionalized PGMA porous monolith was fabricated. • The adsorption capacity of Cu{sup 2+} was 35.3 mg/g. • The effects of porous structure on the adsorption of Cu{sup 2+} were studied. • The adsorption behaviors of porous monolith were studied. - Abstract: The interfacial functionalized poly (glycidyl methacrylate) (PGMA) porous monolith was fabricated and applied as a novel porous adsorbent for copper ions (Cu{sup 2+}). PGMA porous material with highly interconnected pore network was prepared by concentrated emulsion polymerization template. Then polyacrylic acid (PAA) was grafted onto the interface of the porous monolith by the reaction between the epoxy group on PGMA and a carboxyl group on PAA. Finally, the porous monolith was interfacial functionalized by rich amount of carboxyl groups and could adsorb copper ions effectively. The chemical structure and porous morphology of the porous monolith were measured by Fourier transform infrared spectroscopy and scanning electron microscopy. Moreover, the effects of pore size distribution, pH value, co-existing ions, contacting time, and initial concentrations of copper ions on the adsorption capacity of the porous adsorbents were studied.

  1. Solvent-free fabrication of porous polymer for tissue engineering applications

    Science.gov (United States)

    Wang, Xiaoxi

    Tissue engineering scaffold is one of the basic components of all tissue engineering approaches. Most of the existing fabrication techniques for tissue engineering scaffolds require the use of organic solvents that may never be fully removed, even after long processing hours. The residuals of these organic solvents reduce the ability of cells to form new tissues in vivo. In this research, a solvent-free approach to fabricating porous polymers was developed for potential tissue engineering applications. The method includes solid-state foaming and ultrasound treatment. PLA (Polylactic acid), one of the most popular materials in tissue engineering applications, was investigated. The PLA-CO2 system was characterized in this study for the solid-state foaming process with a particular goal of producing low density foams. The results show that low relative density foams (lower than 10%) could be achieved in a wide processing window. To better control the solid-state foaming process and tailor the material properties, a systematic study was carried out on the crystallization behavior of PLA at different stages of the solid-state foaming process. It is found that crystallinity increased linearly with the square root of the area strain of the porous structures. Ultrasound of 20 and 40 kHz was applied to the solid-state foams. Both dye diffusion tests and permeability measurements show that ultrasound could enhance the interconnectivity of solid-state foams. Effects of ultrasound processing time, ultrasound frequency, ultrasound power, bath temperature, and pore size were investigated. For PLA and PETG (Polyethylene Terephthalate Glycol) foams, interconnected microstructures were obtained, with permeability on the level of 10-12 m2 or higher for the pore sizes ranging from 230 mum to 430 mum. Ultrasound heating in the specimen was studied. The maximum temperature induced by the ultrasound heating was found to be below the Tg of PLA. It is proposed that ultrasound cavitation

  2. Water Transport in the Micro Porous Layer and Gas Diffusion Layer of a Polymer Electrolyte Fuel Cell

    Science.gov (United States)

    Qin, C.; Hassanizadeh, S. M.

    2015-12-01

    In this work, a recently developed dynamic pore-network model is presented [1]. The model explicitly solves for both water pressure and capillary pressure. A semi-implicit scheme is used in updating water saturation in each pore body, which considerably increases the numerical stability at low capillary number values. Furthermore, a multiple-time-step algorithm is introduced to reduce the computational effort. A number of case studies of water transport in the micro porous layer (MPL) and gas diffusion layer (GDL) are conducted. We illustrate the role of MPL in reducing water flooding in the GDL. Also, the dynamic water transport through the MPL-GDL interface is explored in detail. This information is essential to the reduced continua model (RCM), which was developed for multiphase flow through thin porous layers [2, 3]. C.Z. Qin, Water transport in the gas diffusion layer of a polymer electrolyte fuel cell: dynamic pore-network modeling, J Electrochimical. Soci., 162, F1036-F1046, 2015. C.Z. Qin and S.M. Hassanizadeh, Multiphase flow through multilayers of thin porous media: general balance equations and constitutive relationships for a solid-gas-liquid three-phase system, Int. J. Heat Mass Transfer, 70, 693-708, 2014. C.Z. Qin and S.M. Hassanizadeh, A new approach to modeling water flooding in a polymer electrolyte fuel cell, Int. J. Hydrogen Energy, 40, 3348-3358, 2015.

  3. Three-dimensional culture of rat calvarial osteoblasts in porous biodegradable polymers

    Science.gov (United States)

    Ishaug-Riley, S. L.; Crane-Kruger, G. M.; Yaszemski, M. J.; Mikos, A. G.

    1998-01-01

    Neonatal rat calvarial osteoblasts were cultured in 90% porous, 75:25 poly(DL-lactic-co-glycolic acid) (PLGA) foam scaffolds for up to 56 days to examine the effects of the cell seeding density, scaffold pore size, and foam thickness on the proliferation and function of the cells in this three-dimensional environment. Osteoblasts were seeded at either 11.1 x 10(5) or 22.1 x 10(5) cells per cm2 onto PLGA scaffolds having pore sizes in the range of 150-300 or 500-710 microm with a thickness of either 1.9 or 3.2 mm. After 1 day in culture, 75.6 and 68.6% of the seeded cells attached and proliferated on the 1.9 mm thick scaffolds of 150-300 microm pore size for the low and high seeding densities, respectively. The number of osteoblasts continued to increase throughout the study and eventually leveled off near 56 days, as indicated by a quantitative DNA assay. Osteoblast/foam constructs with a low cell seeding density achieved comparable DNA content and alkaline phosphatase (ALPase) activity after 14 days, and mineralization results after 56 days to those with a high cell seeding density. A maximum penetration depth of osseous tissue of 220+/-40 microm was reached after 56 days in the osteoblast/foam constructs of 150-300 microm pore size initially seeded with a high cell density. For constructs of 500-710 microm pore size, the penetration depth was 190+/-40 microm under the same conditions. Scaffold pore size and thickness did not significantly affect the proliferation or function of osteoblasts as demonstrated by DNA content, ALPase activity, and mineralized tissue formation. These data show that comparable bone-like tissues can be engineered in vitro over a 56 day period using different rat calvarial osteoblast seeding densities onto biodegradable polymer scaffolds with pore sizes in the range of 150-710 microm. When compared with the results of a previous study where similar polymer scaffolds were seeded and cultured with marrow stromal cells, this study

  4. High CO2-capture ability of a porous organic polymer bifunctionalized with carboxy and triazole groups.

    Science.gov (United States)

    Xie, Lin-Hua; Suh, Myunghyun Paik

    2013-08-26

    A new porous organic polymer, SNU-C1, incorporating two different CO2 -attracting groups, namely, carboxy and triazole groups, has been synthesized. By activating SNU-C1 with two different methods, vacuum drying and supercritical-CO2 treatment, the guest-free phases, SNU-C1-va and SNU-C1-sca, respectively, were obtained. Brunauer-Emmett-Teller (BET) surface areas of SNU-C1-va and SNU-C1-sca are 595 and 830 m(2) g(-1), respectively, as estimated by the N2-adsorption isotherms at 77 K. At 298 K and 1 atm, SNU-C1-va and SNU-C1-sca show high CO2 uptakes, 2.31 mmol  g(-1) and 3.14 mmol  g(-1), respectively, the high level being due to the presence of abundant polar groups (carboxy and triazole) exposed on the pore surfaces. Five separation parameters for flue gas and landfill gas in vacuum-swing adsorption were calculated from single-component gas-sorption isotherms by using the ideal adsorbed solution theory (IAST). The data reveal excellent CO2-separation abilities of SNU-C1-va and SNU-C1-sca, namely high CO2-uptake capacity, high selectivity, and high regenerability. The gas-cycling experiments for the materials and the water-treated samples, experiments that involved treating the samples with a CO2-N2 gas mixture (15:85, v/v) followed by a pure N2 purge, further verified the high regenerability and water stability. The results suggest that these materials have great potential applications in CO2 separation.

  5. Structures and properties of porous coordination polymers based on lanthanide carboxylate building units.

    Science.gov (United States)

    Han, Yinfeng; Li, Xiaoyan; Li, Liqing; Ma, Chunlin; Shen, Zhen; Song, You; You, Xiaozeng

    2010-12-06

    A series of 3-D lanthanide porous coordination polymers, [Ln(6)(BDC)(9)(DMF)(6)(H(2)O)(3)·3DMF](n) [Ln = La, 1; Ce, 2; Nd, 3], [Ln(2)(BDC)(3)(DMF)(2)(H(2)O)(2)](n) [Ln = Y, 4; Dy, 5; Eu, 6], [Ln(2)(ADB)(3)(DMSO)(4)·6DMSO·8H(2)O](n) [Ln = Ce, 7; Sm, 8; Eu, 9; Gd, 10], {[Ce(3)(ADB)(3)(HADB)(3)]·30DMSO·29H(2)O}(n) (11), and [Ce(2)(ADB)(3)(H(2)O)(3)](n) (12) (H(2)BDC = benzene-1,4-dicarboxylic acid and H(2)ADB = 4,4'-azodibenzoic acid), have been synthesized and characterized. In 1-3, the adjacent Ln(III) ions are intraconnected to form 1-D metal-carboxylate oxygen chain-shaped building units, [Ln(4)(CO(2))(12)](n), that constructed a 3-D framework with 4 × 7 Å rhombic channels. In 4-6, the dimeric Ln(III) ions are interlinked to yield scaffolds with 3-D interconnecting tunnels. Compounds 7-10 are all 3-D interpenetrating structures with the CaB6-type topology structure. Compound 11 is constructed by ADB spacers and trinulcear Ce nodes with a NaCl-type topology structure and a 1.9-nm open channel system. In 12, the adjacent Ce(III) ions are intraconnected to form 1-D metal-carboxylate oxygen chain-shaped building units, [Ln(4)(CO(2))(12)](n), and give rise to a 3-D framework. Moreover, 6 exhibits characteristic red luminescence properties of Eu(III) complexes. The magnetic susceptibilities, over a temperature range of 1.8-300 K, of 3, 6, and 7 have also been investigated; the results show paramagnetic properties.

  6. Fabrication of enzyme reactor utilizing magnetic porous polymer membrane for screening D-Amino acid oxidase inhibitors.

    Science.gov (United States)

    Jiang, Jun Fang; Qiao, Juan; Mu, Xiao Yu; Moon, Myeong Hee; Qi, Li

    2017-04-01

    In this work, a unique D-amino acid oxidase reactor for enhanced enzymolysis efficiency is presented. A kind of magnetic polymer matrices, composed of iron oxide nanoparticles and porous polymer membrane (poly styrene-co-maleic anhydride), was prepared. With covalent bonding D-Amino acid oxidase on the surface of the matrices and characterization of scanning electron microscope and vibrating sample magnetometer, it demonstrated that the membrane enzyme reactor was successfully constructed. The enzymolysis efficiency of the enzyme reactor was evaluated and the apparent Michaelis-Menten constants of D-Amino acid oxidase were determined (Km was 1.10mM, Vmax was 23.8mMmin(-1)) by a chiral ligand exchange capillary electrophoresis protocol with methionine as the substrate. The results indicated that the enzyme reactor could exhibit good stability and excellent reusability. Importantly, because the enzyme and the substrate could be confined into the pores of the matrices, the enzyme reactor displayed the improved enzymolysis efficiency due to the confinement effect. Further, the prepared enzyme reactor was applied for D-Amino acid oxidase inhibitors screening. It has displayed that the proposed protocol could pave a new way for fabrication of novel porous polymer membrane based enzyme reactors to screen enzyme inhibitors.

  7. Correlation to Predict Collision Efficiency of Natural Organic Matter (NOM)- and Polymer- coated Nanoparticles in Porous Media

    Science.gov (United States)

    Lowry, G. V.; Phenrat, T.; Cisneros, C. M.; Schoenfelder, D. P.; Fagerlund, F.; Kim, H.; Illangasekare, T.; Tilton, R. D.

    2008-12-01

    The fate of manufactured nanoparticles released to the environment is of great interest due to their increasing use in consumer products and their potential risk to the environment and human health. Manufactured nanomaterials typically have a polymeric surface coating to provide specific functionality, or will adsorb natural organic matter (NOM) once released into the environment. Adsorbed polymer and NOM can provide electrosteic repulsions that enhance the migration of nanoparticles in porous media. Semi-empirical correlations to predict the collision efficiency of electrostatically stabilized (uncoated) colloids are available, however, they are not applicable to nanomaterials coated with polymeric or NOM layers. We present a semi- empirical correlation to predict the collision efficiency of NOM and polymer-coated nanomaterials in saturated porous media. The adsorbed mass and adsorbed layer properties (including thickness) are determined and particle breakthrough curves are generated for a number of particle and coating types. Regression analysis is then used to develop a semi-empirical correlation that includes a parameter (NLEK) representing electrosteric repulsions afforded by adsorbed NOM or polymer. The correlation appears robust over a range of four particle and four coating types and should be a valuable tool for predicting the relative mobility of different manufactured and natural nanomaterials based on a few measurable properties.

  8. Highly Efficient Electrocatalysts for Oxygen Reduction Reaction Based on 1D Ternary Doped Porous Carbons Derived from Carbon Nanotube Directed Conjugated Microporous Polymers

    KAUST Repository

    He, Yafei

    2016-10-11

    © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.One-dimensional (1D) porous materials have shown great potential for gas storage and separation, sensing, energy storage, and conversion. However, the controlled approach for preparation of 1D porous materials, especially porous organic materials, still remains a great challenge due to the poor dispersibility and solution processability of the porous materials. Here, carbon nanotube (CNT) templated 1D conjugated microporous polymers (CMPs) are prepared using a layer-by-layer method. As-prepared CMPs possess high specific surface areas of up to 623 m2 g-1 and exhibit strong electronic interactions between p-type CMPs and n-type CNTs. The CMPs are used as precursors to produce heteroatom-doped 1D porous carbons through direct pyrolysis. As-produced ternary heteroatom-doped (B/N/S) 1D porous carbons possess high specific surface areas of up to 750 m2 g-1, hierarchical porous structures, and excellent electrochemical-catalytic performance for oxygen reduction reaction. Both of the diffusion-limited current density (4.4 mA cm-2) and electron transfer number (n = 3.8) for three-layered 1D porous carbons are superior to those for random 1D porous carbon. These results demonstrate that layered and core-shell type 1D CMPs and related heteroatom-doped 1D porous carbons can be rationally designed and controlled prepared for high performance energy-related applications.

  9. Ion conductivity and transport by porous coordination polymers and metal-organic frameworks.

    Science.gov (United States)

    Horike, Satoshi; Umeyama, Daiki; Kitagawa, Susumu

    2013-11-19

    Ion conduction and transport in solids are both interesting and useful and are found in widely distinct materials, from those in battery-related technologies to those in biological systems. Scientists have approached the synthesis of ion-conductive compounds in a variety of ways, in the areas of organic and inorganic chemistry. Recently, based on their ion-conducting behavior, porous coordination polymers (PCPs) and metal-organic frameworks (MOFs) have been recognized for their easy design and the dynamic behavior of the ionic components in the structures. These PCP/MOFs consist of metal ions (or clusters) and organic ligands structured via coordination bonds. They could have highly concentrated mobile ions with dynamic behavior, and their characteristics have inspired the design of a new class of ion conductors and transporters. In this Account, we describe the state-of-the-art of studies of ion conductivity by PCP/MOFs and nonporous coordination polymers (CPs) and offer future perspectives. PCP/MOF structures tend to have high hydrophilicity and guest-accessible voids, and scientists have reported many water-mediated proton (H(+)) conductivities. Chemical modification of organic ligands can change the hydrated H(+) conductivity over a wide range. On the other hand, the designable structures also permit water-free (anhydrous) H(+) conductivity. The incorporation of protic guests such as imidazole and 1,2,4-triazole into the microchannels of PCP/MOFs promotes the dynamic motion of guest molecules, resulting in high H(+) conduction without water. Not only the host-guest systems, but the embedding of protic organic groups on CPs also results in inherent H(+) conductivity. We have observed high H(+) conductivities under anhydrous conditions and in the intermediate temperature region of organic and inorganic conductors. The keys to successful construction are highly mobile ionic species and appropriate intervals of ion-hopping sites in the structures. Lithium (Li

  10. Highly porous organic polymers bearing tertiary amine group and their exceptionally high CO{sub 2} uptake capacities

    Energy Technology Data Exchange (ETDEWEB)

    Gomes, Ruth; Bhaumik, Asim, E-mail: msab@iacs.res.in

    2015-02-15

    We report a very simple and unique strategy for synthesis of a tertiary amine functionalized high surface area porous organic polymer (POP) PDVTA-1 through the co-polymerization of monomers divinylbenzene (DVB) and triallylamine (TAA) under solvothermal reaction conditions. Two different PDVTA-1 samples have been synthesized by varying the molar ratio of the monomers. The porous polymeric materials have been thoroughly characterized by solid state {sup 13}C CP MAS-NMR, FT-IR and UV–vis spectroscopy, N{sub 2} sorption, HR TEM and FE SEM to understand its chemical environment, nanostructure, bonding, morphology and related surface properties. PDVTA-1 with higher amine content (DVB/TAA=4.0) showed exceptionally high CO{sub 2} uptake capacity of 85.8 wt% (19.5 mmol g{sup −1}) at 273 K and 43.69 wt% (9.93 mmol g{sup −1}) at 298 K under 3 bar pressure, whereas relatively low amine loaded material (DVB/TAA=7.0) shows uptake capacity of 59.2 wt% (13.45 mmol g{sup −1}) at 273 K and 34.36 wt% (7.81 mmol g{sup −1}) at 298 K. Highly porous nanostructure together with very high surface area and basicity at the surface due to the presence of abundant basic tertiary amine N-sites in the framework of PDVTA-1 could be responsible for very high CO{sub 2} adsorption. - Graphical abstract: Exceptionally high CO2 uptake (85.8 wt % at 273 K) has been observed over a high surface area porous organic polymer PDVTA-1 synthesized through copolymerization of divinylbenzene and triallyl amine. - Highlights: • Designing the synthesis of a new N-rich cross-linked porous organic polymer PDVTA-1. • PDVTA-1 showed mesoporosity with very high surface area of 903 m{sup 2} g{sup −1}. • High surface area and presence of basic sites facilitates the CO{sub 2} uptake. • PDVTA-1 showed exceptionally high CO{sub 2} adsorption capacity of 85.8 wt% at 273 K, 3 bar pressure.

  11. Polymeric molecular sieve membranes via in situ cross-linking of non-porous polymer membrane templates

    Science.gov (United States)

    Qiao, Zhen-An; Chai, Song-Hai; Nelson, Kimberly; Bi, Zhonghe; Chen, Jihua; Mahurin, Shannon M.; Zhu, Xiang; Dai, Sheng

    2014-04-01

    High-performance polymeric membranes for gas separation are attractive for molecular-level separations in industrial-scale chemical, energyand environmental processes. Molecular sieving materials are widely regarded as the next-generation membranes to simultaneously achieve high permeability and selectivity. However, most polymeric molecular sieve membranes are based on a few solution-processable polymers such as polymers of intrinsic microporosity. Here we report an in situ cross-linking strategy for the preparation of polymeric molecular sieve membranes with hierarchical and tailorable porosity. These membranes demonstrate exceptional performance as molecular sieves with high gas permeabilities and selectivities for smaller gas molecules, such as carbon dioxide and oxygen, over larger molecules such as nitrogen. Hence, these membranes have potential for large-scale gas separations of commercial and environmental relevance. Moreover, this strategy could provide a possible alternative to ‘classical’ methods for the preparation of porous membranes and, in some cases, the only viable synthetic route towards certain membranes.

  12. PEG encapsulated by porous triamide-linked polymers as support for solid-liquid phase change materials for energy storage

    Science.gov (United States)

    Andriamitantsoa, Radoelizo S.; Dong, Wenjun; Gao, Hongyi; Wang, Ge

    2017-03-01

    A series of porous triamide-linked polymers labeled as PTP were prepared by condensation of 1,3,5-benzenetricarbonyl trichloride with benzene-1,4-diamine (A), 4,4‧-methylenediamine (B) and 1,3,5-triazine-2,4,6-triamine (C) respectively. The as-synthesized polymers exhibit permanent porosity and high surface areas which guarantee to hold polyethylene glycol (PEG) molecules in their network for shape-stabilized phase change materials. They possess different effects on the phase change properties of the composite due to their different porosities. PTP-A have intrinsic well-ordered morphology, microstructure and good enough pores to keep the PCMs compared to PTP-B and PTP-C. PEG 2000 used as PCMs could be retained up to 85 wt% in PTP-A polymer materials and these composites were defined as form-stable composite PCMs without the leakage of melted PCM. The thermal study revealed a good storage effect of encapsulated polymer and the enthalpy of melting increases in the order PTP-C storage capacity. The latent heats for melting and freezing was found to be 155 and 141.7 kJ/kg with a peak appearing at around 53.13 and 29.67 °C respectively. The study suggests that pore size is important for the preparation of shape-stabilized PCMs.

  13. Porous polymer coatings as substrates for the formation of high-fidelity micropatterns by quill-like pens

    Directory of Open Access Journals (Sweden)

    Michael Hirtz

    2013-06-01

    Full Text Available We explored the potentials of microarray printing using quill-like microcantilevers onto solid supports that are typically used in microspot printing, including paper, polymeric nitrocellulose and nylon membranes. We compared these membranes with a novel porous poly(2-hydroxyethyl methacrylate-co-ethylene dimethacrylate support (HEMA with narrow pore size distribution in the 150 nm range, which demonstrated advantages in pattern definition, spot homogeneity, and consistent spot delivery of different dyes (phloxine B and bromophenol blue with diameters of several micrometres. The bromophenol blue arrays on HEMA support were used to detect the presence of bovine serum albumin (BSA. In the presence of BSA, the fluorescence spectrum observed from the bromophenol blue microarray exhibited a significant red shift of the maximum emission wavelength. Our results show that the porous HEMA substrates can improve the fidelity and quality of microarrays prepared by using the quill-like microcantilevers. The presented method sets the stage for further studies using chemical and biochemical recognition elements, along with colorimetric and fluorometric sensors that can be spotted by this method onto flat porous polymer substrates.

  14. Metallosalen-Based Ionic Porous Polymers as Bifunctional Catalysts for the Conversion of CO2 into Valuable Chemicals.

    Science.gov (United States)

    Luo, Rongchang; Chen, Yaju; He, Qian; Lin, Xiaowei; Xu, Qihang; He, Xiaohui; Zhang, Wuying; Zhou, Xiantai; Ji, Hongbing

    2016-12-31

    A series of new metallosalen-based ionic porous organic polymers (POPs) were synthesized for the first time using a simple unique strategy based on the free-radical copolymerization reaction. Various techniques were used to characterize the physicochemical properties of these catalysts. These well-designed materials endowed high surface area, hierarchical porous structures, and enhanced CO2 /N2 adsorptive selectivity. Moreover, these POPs having both metal centers (Lewis acid) and ionic units (nucleophile) could serve as bifunctional catalysts in the catalytic conversion of CO2 into high value-added chemicals without any additional co-catalyst under mild and solvent-free conditions, for example, CO2 /epoxides cycloaddition and Nformylation of amines from CO2 and hydrosilanes. The results demonstrated that the irregular porous structure was very favorable for the diffusion of substrates and products, and the microporous structural property resulted in the enrichment of CO2 near the catalytic centers in the CO2 -involved transformations. Additionally, the superhydrophobic property could not only enhance the chemoselectivity of products but also promote the stability and recyclability of catalysts.

  15. Improved manufacturing technology for producing porous Nafion for high-performance ionic polymer-metal composite actuators

    Science.gov (United States)

    Zhao, Dongxu; Li, Dichen; Wang, Yanjie; Chen, Hualing

    2016-07-01

    The current actuation performance of ionic polymer-metal composites (IPMCs) limits their further application in the aerospace, energy, and optics fields, among others. To overcome this issue, we developed a freeze-drying process to generate Nafion membranes with a porous structure, the characteristics of which were investigated using thermogravimetric analysis, Fourier transform infrared spectrometry, field-emission scanning electron microscopy, and water uptake tests. The pores fabricated using the developed freeze-drying process had a diameter of approximately 270 nm, and a porosity of nearly 40.45%. The displacement and the central angle were introduced as variables to evaluate the bending deformation of an IPMC actuator based on the porous Nafion membrane. Compared with conventional actuators, this IPMC actuator showed an increase in displacement of 4963.6% at 2 V, and an increase in central angle of 73.35% at 3 V. Although the blocking forces of this IPMC actuator decreased to some extent, it was confirmed that the integrated actuation performance, which was evaluated using the strain energy density increment, was improved. The performance of the IPMC actuator was enhanced as a result of the porous Nafion structure manufactured using the developed freeze-drying process.

  16. Porous Ionic Polymers as a Robust and Efficient Platform for Capture and Chemical Fixation of Atmospheric CO2.

    Science.gov (United States)

    Sun, Qi; Jin, Yingyin; Aguila, Briana; Meng, Xiangju; Ma, Shengqian; Xiao, Feng-Shou

    2017-03-22

    Direct use of atmospheric CO2 as a C1 source to synthesize high-value chemicals through environmentally benign processes is of great interest, yet challenging. Porous heterogeneous catalysts that are capable of simultaneously capturing and converting CO2 are promising candidates for such applications. Herein, a family of organic ionic polymers with nanoporous structure, large surface area, strong affinity for CO2 , and very high density of catalytic active sites (halide ions) was synthesized through the free-radical polymerization of vinylfunctionalized quaternary phosphonium salts. The resultant porous ionic polymers (PIPs) exhibit excellent activities in the cycloaddition of epoxides with atmospheric CO2 , outperforming the corresponding soluble phosphonium salt analogues and ranking among the highest of known metal-free catalytic systems. The high CO2 uptake capacity of the PIPs facilitates the enrichment of CO2 molecules around the catalytic centers, thereby benefiting its conversion. We have demonstrated for the first time that atmospheric CO2 can be directly converted to cyclic carbonates at room temperature using a heterogeneous catalytic system under metal-solvent free conditions. Moreover, the catalysts proved to be robust and fully recyclable, demonstrating promising potential for practical utilization for the chemical fixation of CO2 . Our work thereby paves a way to the advance of PIPs as a new type of platform for capture and conversion of CO2 .

  17. Modulation of anabolic and catabolic responses via a porous polymer scaffold manufactured using thermally induced phase separation

    Directory of Open Access Journals (Sweden)

    A Schindeler

    2013-02-01

    Full Text Available We describe two studies encompassing the iterative refinement of a polymer-based rhBMP-2 delivery system for bone tissue engineering. Firstly, we compared the bone-forming capacity of porous poly(D,L-lactic-co-glycolic acid (PLGA scaffolds produced by thermally induced phase separation (TIPS with non-porous solvent cast poly(D,L-lactic acid (PDLLA used previously. Secondly, we examined the potential synergy between rhBMP-2 and local bisphosphonate in the PLGA scaffold system.In vivo ectopic bone formation studies were performed in C57BL6/J mice. Polymer scaffolds containing 0, 5, 10 or 20 µg rhBMP-2 were inserted into the dorsal musculature. At all rhBMP-2 doses, porous PLGA produced significantly higher bone volume (BV, mm3 than the solid PDLLA scaffolds. Next, porous PLGA scaffolds containing 10 µg rhBMP-2 ± 0.2, or 2 µg zoledronic acid (ZA were inserted into the hind-limb musculature. Co-delivery of local 10 µg rhBMP-2/2 µg ZA significantly augmented bone formation compared with rhBMP-2 alone (400 % BV increase, p < 0.01. Hydroxyapatite microparticle (HAp addition (2 % w/w to the 10 µg rhBMP-2/0.2 µg ZA group increased BV (200 %, p < 0.01. We propose that this was due to controlled ZA release of HAp-bound ZA. Consistent with this, elution analyses showed that HAp addition did not alter the rhBMP-2 elution, but delayed ZA release. Moreover, 2 % w/w HAp addition reduced the scaffold’s compressive properties, but did not alter ease of surgical handling.In summary, our data show that refinement of the polymer selection and scaffold fabrication can enhance rhBMP-2 induced bone formation in our bone tissue engineering implant, and this can be further optimised by the local co-delivery of ZA/HAp.

  18. The measurement of the shear modulus for polymer porous layer with two microphones

    OpenAIRE

    2009-01-01

    International audience; An experimental method is described for measuring the shear modulus of thin porous layer. An acoustical excitation with a loudspeaker and a simulation performed with the Biot theory allow measurement without any mechanical excitation.

  19. Fabrication of a multifunctional nano-in-micro drug delivery platform by microfluidic templated encapsulation of porous silicon in polymer matrix.

    Science.gov (United States)

    Zhang, Hongbo; Liu, Dongfei; Shahbazi, Mohammad-Ali; Mäkilä, Ermei; Herranz-Blanco, Bárbara; Salonen, Jarno; Hirvonen, Jouni; Santos, Hélder A

    2014-07-01

    A multifunctional nano-in-micro drug delivery platform is developed by conjugating the porous silicon nanoparticles with mucoadhesive polymers and subsequent encapsulation into a pH-responsive polymer using microfluidics. The multistage platform shows monodisperse size distribution and pH-responsive payload release, and the released nanoparticles are mucoadhesive. Moreover, this platform is capable of simultaneously loading and releasing multidrugs with distinct properties.

  20. Self-diffusion of nonfreezing water in porous carbohydrate polymer systems studied with nuclear magnetic resonance.

    Science.gov (United States)

    Topgaard, Daniel; Söderman, Olle

    2002-12-01

    Water is an integral part of the structure in biological porous materials such as wood and starch. A problem often encountered in the preparation of samples for, e.g., electron microscopy is that removal of water leads to a decreasing distance between supermolecular structural elements and a distortion of the structure. It is, therefore, of interest to find methods to investigate these materials in the native water-swollen state. We present a method to study water-swollen biological porous structures using NMR to determine the amount and self-diffusion of water within the porous objects. The contribution of bulk water to the NMR signal is eliminated by performing experiments below the bulk freezing temperature. Further decrease of the temperature leads to a gradual freezing of water within the porous objects. The contribution of the freezing water fraction to the migration of water through the porous network is, thus, estimated. The results are rationalized in terms of the ultrastructure of the samples studied, namely, wood pulp fibers and potato starch granules.

  1. PVdF-HFP/metal oxide nanocomposites: The matrices for high-conducting, low-leakage porous polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Chun-Guey; Lu, Ming-I.; Tsai, Chung-Chih [Department of Chemistry, National Central University, Chung-Li, Taiwan 32054 (ROC); Chuang, Huey-Jan [Chung-Shan Institute of Science and Technology, Materials and Electro-Optics Research Division, Lung-Tan, Taiwan 325 (ROC)

    2006-09-13

    Highly conducting porous polymer electrolytes comprised of poly(vinylidene-fluoride-co-hexafluoropropylene) (PVdF-HFP), metal oxide (TiO{sub 2}, MgO, ZnO)/or mesoporous zeolite (MCM-41, SBA-15), ethylene carbonate (EC), propylene carbonate (PC), and LiClO{sub 4} were fabricated with a simple direct evaporation method. It was found that when metal oxide or mesoporous zeolite was mixed with PVdF-HFP, the impedance spectroscopy showed that the room temperature conductivity increased from 1.2x10{sup -3}Scm{sup -1} (for pure PVdF-HFP) to 2.1x10{sup -3}Scm{sup -1}. SEM micrographs showed that the pore size of the composite membrane was similar to that of pure PVdF-HFP membrane but the porosity decreased, nevertheless the solution uptake increased. The increasing in solution uptake is not related directly to the surface area or dielectric constant of the oxides. It may be due to the affinity of the metal oxide toward the electrolyte solution. Furthermore, the solution leakage of PVdF-HFP/MgO and PVdF-HFP/SBA-15 composite electrolytes also decreased compared to pure PVdF-HFP electrolyte. These polymer composite electrolytes were stable up to 5.5V (versus Li/Li{sup +}) and the lithium ion cells assembled with these polymer electrolyte show a good performance at a discharge rate below C/2. (author)

  2. PVdF-HFP/metal oxide nanocomposites: The matrices for high-conducting, low-leakage porous polymer electrolytes

    Science.gov (United States)

    Wu, Chun-Guey; Lu, Ming-I.; Tsai, Chung-Chih; Chuang, Huey-Jan

    Highly conducting porous polymer electrolytes comprised of poly(vinylidene-fluoride-co-hexafluoropropylene) (PVdF-HFP), metal oxide (TiO 2, MgO, ZnO)/or mesoporous zeolite (MCM-41, SBA-15), ethylene carbonate (EC), propylene carbonate (PC), and LiClO 4 were fabricated with a simple direct evaporation method. It was found that when metal oxide or mesoporous zeolite was mixed with PVdF-HFP, the impedance spectroscopy showed that the room temperature conductivity increased from 1.2 × 10 -3 S cm -1 (for pure PVdF-HFP) to 2.1 × 10 -3 S cm -1. SEM micrographs showed that the pore size of the composite membrane was similar to that of pure PVdF-HFP membrane but the porosity decreased, nevertheless the solution uptake increased. The increasing in solution uptake is not related directly to the surface area or dielectric constant of the oxides. It may be due to the affinity of the metal oxide toward the electrolyte solution. Furthermore, the solution leakage of PVdF-HFP/MgO and PVdF-HFP/SBA-15 composite electrolytes also decreased compared to pure PVdF-HFP electrolyte. These polymer composite electrolytes were stable up to 5.5 V (versus Li/Li +) and the lithium ion cells assembled with these polymer electrolyte show a good performance at a discharge rate below C/2.

  3. The influence of surface topography of a porous perfluoropolyether polymer on corneal epithelial tissue growth and adhesion.

    Science.gov (United States)

    Evans, Margaret D M; Chaouk, Hassan; Wilkie, John S; Dalton, Beatrice A; Taylor, Sarah; Xie, Ruo Zhong; Hughes, Timothy C; Johnson, Graham; McFarland, Gail A; Griesser, Hans H; Steele, John G; Meijs, Gordon F; Sweeney, Deborah F; McLean, Keith M

    2011-12-01

    Design principles for corneal implants are challenging and include permeability which inherently involves pore openings on the polymer surface. These topographical cues can be significant to a successful clinical outcome where a stratified epithelium is needed over the device surface, such as with a corneal onlay or corneal repair material. The impact of polymer surface topography on the growth and adhesion of corneal epithelial tissue was assessed using porous perfluoropolyether membranes with a range of surface topography. Surfaces were characterised by AFM and XPS, and the permeability and water content of membranes was measured. Biological testing of membranes involved a 21-day in vitro tissue assay to evaluate migration, stratification and adhesion of corneal epithelium. Similar parameters were monitored in vivo by surgically implanting membranes into feline corneas for up to 5 months. Data showed optimal growth and adhesion of epithelial tissue in vitro when polymer surface features were below a 150 nm RMS value. Normal processes of tissue growth and adhesion were disrupted when RMS values approached 300 nm. Data from the in vivo study confirmed these findings. Together, outcomes demonstrated the importance of surface topography in the design of implantable devices that depend on functional epithelial cover.

  4. Enrichment of steroid hormones in water with porous and hydrophobic polymer-based SPE followed by HPLC-UV determination.

    Science.gov (United States)

    Hu, Yinfen; Zhang, Man; Tong, Changlun; Wu, Jianmin; Liu, Weiping

    2013-10-01

    There have been great concerns about the persistence of steroid hormones in surface water. Since the concentrations of these compounds in water samples are usually at a trace level, the efficient enrichment of steroid hormones is vital for further analysis. In this work, a porous and hydrophobic polymer was synthesized and characterized. The composition of solvent used as porogen in the synthetic process was shown to have an effect on the morphology of the polymer, which was successfully used as an SPE sorbent for simultaneously enriching steroid hormones in surface water samples. The recoveries of the steroid hormones on the custom-made polymer ranged from 93.4 to 106.2%, whereas those on commercialized ENVI-18, LC-18, and Oasis HLB ranged from 54.8 to 104.9, 66 to 93.6, and 77.2 to 106%, respectively. Five types of steroid hormones were simultaneously measured using HPLC-UV after they were enriched by the custom-made sorbent. Based on these findings, the SPE-HPLC method was developed. The LODs of this method for estriol, estradiol, estrone, androstenedione, progesterone were 0.07, 0.43, 0.61, 0.27, and 0.42 μg/L, respectively, while precision and reproducibility RSDs were <6.40 and 7.49%, respectively.

  5. High-performance supercapacitor based on nitrogen-doped porous carbon derived from zinc(II)-bis(8-hydroxyquinoline) coordination polymer.

    Science.gov (United States)

    Chen, Xiang Ying; Xie, Dong Hua; Chen, Chong; Liu, Jian Wei

    2013-03-01

    Nitrogen-doped porous carbon electrodes with remarkable specific capacitance have been fabricated by the rational carbonization of zinc(II)-bis(8-hydroxyquinoline) (abbr. Znq(2)) coordination polymer, and heating treatment with CO(NH(2))(2). The experimental results demonstrate that the mass ratio of carbon precursor and CO(NH(2))(2) plays a key role in the formation of porous carbon with various nitrogen content as well as specific surface areas and pore structures. The cyclic voltammetry and galvanostatic charge-discharge measurements show that the capacitive performance has been remarkably improved by doping with nitrogen. The specific capacitance of 219.2 F g(-1) is achieved at the current density of 1 A g(-1) with nitrogen-doped porous carbon, increasing up to ca. 56.8% compared to that with pristine porous carbon. The nitrogen-doped porous carbon electrode exhibits enhance capacitance retention as ca. 45.2% at 20 A g(-1) as well as cycling stability (ca. 7.6% loss after 3000 cycles). The present carbonization method as well as the nitrogen-doping method for porous carbon from coordination polymer can enrich the strategies for the production of carbon-based electrodes materials in the application of electrochemical capacitors.

  6. Highly selective CO2 adsorption accompanied with low-energy regeneration in a two-dimensional Cu(II) porous coordination polymer with inorganic fluorinated PF6(-) anions.

    Science.gov (United States)

    Noro, Shin-ichiro; Hijikata, Yuh; Inukai, Munehiro; Fukushima, Tomohiro; Horike, Satoshi; Higuchi, Masakazu; Kitagawa, Susumu; Akutagawa, Tomoyuki; Nakamura, Takayoshi

    2013-01-01

    High selectivity and low-energy regeneration for adsorption of CO(2) gas were achieved concurrently in a two-dimensional Cu(II) porous coordination polymer, [Cu(PF(6))(2)(4,4'-bpy)(2)](n) (4,4'-bpy = 4,4'-bipyridine), containing inorganic fluorinated PF(6)(-) anions that can act as moderate interaction sites for CO(2) molecules.

  7. POROUS POLYMER IMPLANTS FOR REPAIR OF FULL-THICKNESS DEFECTS OF ARTICULAR-CARTILAGE - AN EXPERIMENTAL-STUDY IN RABBIT AND DOG

    NARCIS (Netherlands)

    JANSEN, HWB; VETH, RPH; NIELSEN, HKL; DEGROOT, JH; PENNINGS, AJ

    1992-01-01

    Full-thickness defects of articular cartilage were repaired by implantation of porous polymer implants in rabbits and dogs. The quality of the repair tissue was determined by collagen typing with antibodies. Implants with varying pore sizes and chemical composition were used. The effect of loading

  8. Pore-Network Modeling of Water and Vapor Transport in the Micro Porous Layer and Gas Diffusion Layer of a Polymer Electrolyte Fuel Cell

    NARCIS (Netherlands)

    Qin, C.; Hassanizadeh, S.M.; van Oosterhout, L.M.

    2016-01-01

    In the cathode side of a polymer electrolyte fuel cell (PEFC), a micro porous layer (MPL) added between the catalyst layer (CL) and the gas diffusion layer (GDL) plays an important role in water management. In this work, by using both quasi-static and dynamic pore-network models, water and vapor tra

  9. The development of a high-throughput gradient array apparatus for the study of porous polymer networks.

    Energy Technology Data Exchange (ETDEWEB)

    Majumdar, Partha (North Dakota State University, Fargo, ND); Lee, Elizabeth (North Dakota State University, Fargo, ND); Chisholm, Bret J. (North Dakota State University, Fargo, ND); Dirk, Shawn M.; Weisz, Michael (North Dakota State University, Fargo, ND); Bahr, James (North Dakota State University, Fargo, ND); Schiele, Kris (North Dakota State University, Fargo, ND)

    2010-01-01

    A gradient array apparatus was constructed for the study of porous polymers produced using the process of chemically-induced phase separation (CIPS). The apparatus consisted of a 60 element, two-dimensional array in which a temperature gradient was placed in the y-direction and composition was varied in the x-direction. The apparatus allowed for changes in opacity of blends to be monitored as a function of temperature and cure time by taking images of the array with time. The apparatus was validated by dispense a single blend composition into all 60 wells of the array and curing them for 24 hours and doing the experiment in triplicate. Variations in micron scale phase separation were readily observed as a function of both curing time and temperature and there was very good well-to-well consistency as well as trial-to-trial consistency. Poragen of samples varying with respect to cure temperature was removed and SEM images were obtained. The results obtained showed that cure temperature had a dramatic affect on sample morphology, and combining data obtained from visual observations made during the curing process with SEM data can enable a much better understanding of the CIPS process and provide predictive capability through the relatively facile generation of composition-process-morphology relationships. Data quality could be greatly enhanced by making further improvements in the apparatus. The primary improvements contemplated include the use of a more uniform light source, an optical table, and a CCD camera with data analysis software. These improvements would enable quantification of the amount of scattered light generated from individual elements as a function of cure time. In addition to the gradient array development, porous composites were produced by incorporating metal particles into a blend of poragen, epoxy resin, and crosslinker. The variables involved in the experiment were metal particle composition, primary metal particle size, metal concentration

  10. Preparation and Characterization of Nano-polymer Porous MgO

    Institute of Scientific and Technical Information of China (English)

    Xue Liang ZHAI; Ai Dong ZHAO; Mi Ying JIA

    2004-01-01

    Porous carrier MgO which was aggregated by nano-particles has been firstly prepared by using a normal technology route. The MgO was rod-shaped and had large surface area. The factors which affect grain size and microstructure of MgO were explored.

  11. Solvent-free porous framework resulted from 3D entanglement of 1D zigzag coordination polymer

    KAUST Repository

    Kole, Goutam Kumar Umar

    2010-01-01

    A solvent-free porous metal organic framework is constructed by the 3D entanglement of 1D zigzag coordination polymeric chains. The role of solvents and the effect of reaction conditions on such unique entanglement are addressed. © 2010 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.

  12. Dye-sensitized solar cell derived from nano-porous polymer

    DEFF Research Database (Denmark)

    Li, Tao; Ndoni, Sokol

    Nano-porous cross-linked polybutadiene has been used as the template which has good wetting properties with various inorganic precursors. A novel and facile nanocasting process has been developed to fabricate of a thin film with 10-nm wide titania network which is compact, inter-connected, and co...

  13. Hepatic Differentiation of Human Induced Pluripotent Stem Cells in a Perfused 3D Porous Polymer Scaffold for Liver Tissue Engineering

    DEFF Research Database (Denmark)

    Hemmingsen, Mette; Muhammad, Haseena Bashir; Mohanty, Soumyaranjan

    A huge shortage of liver organs for transplantation has motivated the research field of tissue engineering to develop bioartificial liver tissue and even a whole liver. The goal of NanoBio4Trans is to create a vascularized bioartificial liver tissue, initially as a liver-support system. Due...... to limitations of primary hepatocytes regarding availability and maintenance of functionality, stem cells and especially human induced pluripotent stem cells (hIPS cells) are an attractive cell source for liver tissue engineering. The aim of this part of NanoBio4Trans is to optimize culture and hepatic...... differentiation of hIPS-derived definitive endoderm (DE) cells in a 3D porous polymer scaffold built-in a perfusable bioreactor. The use of a microfluidic bioreactor array enables the culture of 16 independent tissues in one experimental run and thereby an optimization study to be performed....

  14. Preparation of hybrid thiol-acrylate emulsion-templated porous polymers by interfacial copolymerization of high internal phase emulsions.

    Science.gov (United States)

    Langford, Caitlin R; Johnson, David W; Cameron, Neil R

    2015-05-01

    Emulsion-templated highly porous polymers (polyHIPEs), containing distinct regions differing in composition, morphology, and/or properties, are prepared by the simultaneous polymerization of two high internal phase emulsions (HIPEs) contained within the same mould. The HIPEs are placed together in the mould and subjected to thiol-acrylate photopolymerization. The resulting polyHIPE material is found to contain two distinct semicircular regions, reflecting the composition of each HIPE. The original interface between the two emulsions becomes a copolymerized band between 100 and 300 μm wide, which is found to be mechanically robust. The separate polyHIPE layers are distinguished from one another by their differing average void diameter, chemical composition, and extent of contraction upon drying.

  15. Porous polymer composite membrane based nanogenerator: A realization of self-powered wireless green energy source for smart electronics applications

    Science.gov (United States)

    Ghosh, Sujoy Kumar; Sinha, Tridib Kumar; Mahanty, Biswajit; Jana, Santanu; Mandal, Dipankar

    2016-11-01

    An efficient, flexible and unvaryingly porous polymer composite membrane based nanogenerator (PPCNG) without any electrical poling treatment has been realised as wireless green energy source to power up smart electronic gadgets. Owing to self-polarized piezo- and ferro-electretic phenomenon of in situ platinum nanoparticles (Pt-NPs) doped porous poly(vinylidenefluoride-co-hexafluoropropylene)-membrane, a simple, inexpensive and scalable PPCNG fabrication is highlighted. The molecular orientations of the -CH2/-CF2 dipoles that cause self-polarization phenomenon has been realized by angular dependent near edge X-ray absorption fine structure spectroscopy. The square-like hysteresis loop with giant remnant polarization, Pr ˜ 68 μC/cm2 and exceptionally high piezoelectric charge coefficient, d33 ˜ - 836 pC/N promises a best suited ferro- and piezo-electretic membrane. The PPCNG exhibits a high electrical throughput such as, ranging from 2.7 V to 23 V of open-circuit voltage (Voc) and 2.9 μA to 24.7 μA of short-circuit current (Isc) under 0.5 MPa to 4.3 MPa of imparted stress amplitude by periodic human finger motion. The harvested mechanical and subsequent electrical energy by PPCNG is shown to transfer wirelessly via visible and infrared transmitter-receiver systems, where 17% and 49% of wireless power transfer efficiency, respectively, has been realized to power up several consumer electronics.

  16. Experimental investigations on the fluid flow mechanism in porous media of enhanced oil recovery by alkli/surfactant/polymer flooding

    Institute of Scientific and Technical Information of China (English)

    WANG Jialu; SHEN Pingping; CHEN Yongzhong; ZHANG Zubo; JIA Xu; TIAN Yuling

    2005-01-01

    The fluid flow mechanism in porous media of enhanced oil recovery by Alkli/ Surfactant/ Polymer (ASP) flooding is investigated by measuring production performance, pressure distribution and saturation distribution through installing differential pressure transducers and saturation measuring probes in a physical model of vertical heterogeneous reservoir. The fluid flow variation in porous media is the main reason of enhanced oil recovery of ASP flooding. The pressure field and saturation field are nonlinearly coupled together and the interaction between them results in the fluid flow variation in the reservoir. In a vertical heterogeneous reservoir, the ASP agents initially flow in the high permeability layer, and fluid changes the flow direction toward the low and the middle permeability layers because the resistance in the high permeability layer is increased under the physical and chemical action of adsorption, retention and emulsion. ASP flooding displaces out not only the residual oil in the high permeability layer, but also the remaining oil in the low and the middle permeability layers by increasing swept volume and displacing efficiency.

  17. Infiltrated Porous Polymer Sheets as Free-Standing Flexible Lithium-Sulfur Battery Electrodes.

    Science.gov (United States)

    Wu, Feixiang; Zhao, Enbo; Gordon, Daniel; Xiao, Yiran; Hu, Chenchen; Yushin, Gleb

    2016-08-01

    Free-standing, high-capacity Li2 S electrodes with capacity loadings in the range from 1.5 to 3.8 mA h cm(-2) are produced by using infiltration of active materials into porous carbonized biomass sheets. The proposed electrode design can be effectively utilized for the low-cost fabrication of flexible lithium batteries with high specific energy.

  18. Effect of the porous structure of polymer foams on the remediation of oil spills

    Science.gov (United States)

    Pinto, Javier; Athanassiou, Athanassia; Fragouli, Despina

    2016-04-01

    Current approaches for the remediation of oil spills propose the utilization of functionalized polymeric foams as efficient oil absorbents. However, for the majority of the materials employed, the studies are focused on sophisticated surface treatments while the significant role of the morphological parameters of the porous structure of the pristine foams remains unexplored. Herein, we prove that the structural parameters of the pores of the polymeric foams play a fundamental role for the efficient removal of oil from water. The presented experimental and theoretical study shows that pristine polyurethane foams with highly interconnected open porous structures, and pore sizes below 500 μm are able to reach oil absorption capacities as high as 30 gr of oil per gr of polyurethane. Chemical functionalization of the porous structure does not increase further the oil absorption efficiency but it significantly contributes to the increase of the selectivity of the process. The current findings demonstrate the importance of the right choice of the pristine foams for the fabrication of cost-effective absorbents with high water-oil separation performance.

  19. Nafion-porous cerium oxide nanotubes composite membrane for polymer electrolyte fuel cells operated under dry conditions

    Science.gov (United States)

    Ketpang, Kriangsak; Oh, Kwangjin; Lim, Sung-Chul; Shanmugam, Sangaraju

    2016-10-01

    A composite membrane operated in polymer electrolyte fuel cells (PEFCs) under low relative humidity (RH) is developed by incorporating cerium oxide nanotubes (CeNT) into a perfluorosulfonic acid (Nafion®) membrane. Porous CeNT is synthesized by direct heating a precursor impregnated polymer fibers at 500 °C under an air atmosphere. Compared to recast Nafion and commercial Nafion (NRE-212) membranes, the Nafion-CeNT composite membrane generates 1.1 times higher power density at 0.6 V, operated at 80 °C under 100% RH. Compared to Nafion-cerium oxide nanoparticles (Nafion-CeNP) membrane, the Nafion-CeNT provides 1.2 and 1.7 times higher PEFC performance at 0.6 V when operated at 80 °C under 100% and 18% RH, respectively. Additionally, the Nafion-CeNT composite membrane exhibits a good fuel cell operation under 18% RH at 80 °C. Specifically, the fluoride emission rate of Nafion-CeNT composite membrane is 20 times lower than that of the commercial NRE-212 membrane when operated under 18% RH at 80 °C for 96 h. The outstanding PEFC performance and durability operated under dry conditions is mainly attributed to the facile water diffusion capability as well as the effective hydroxyl radical scavenging property of the CeNT filler, resulting in significantly mitigating both the ohmic resistance and Nafion membrane degradation.

  20. Flexible porous coordination polymer of Ni(II) for developing nanoparticles through acid formation and redox activity of the framework

    Science.gov (United States)

    Agarwal, Rashmi A.

    2017-10-01

    Immobilization of the nanoparticles (NPs) in a two dimensional porous coordination polymer (PCP) is currently an emerging field for a number of applications. But still it is a great challenge to fabricate any specified metal NPs in a single network. Herein the synthesis of Au, Pd, Mn, Fe, Cu, Zn, Mg, Li, Fe/Cu, Zn/Mg etc, NPs in a highly flexible PCP of Ni(II); {[Ni3(TBIB)2(BTC)2(H2O)6]·5C2H5OH·9H2O}n [TBIB = 1,3,5-tri(1H-benzo[d]imidazol-1-yl)benzene, H3BTC = 1,3,5-benzenetricarboxylic acid] have been reported. This universal host is able to grow mixed metal NPs from mixed metal precursors. Monodentate carboxylate groups of BTC linker act as anchoring sites for the metal ions of the metal precursors. This is the main driving force to grow NPs within the cavities along with the high flexibility of this polymer at room temperature. Mechanism involves acid formation followed by redox reaction to synthesize metal NPs explained by EPR and FTIR. Paramagnetic properties have been shown by as-synthesized Fe NPs integrated framework at room temperature under applied magnetic field up to 17,500 Oe.

  1. Impact of redox-active polymer molecular weight on the electrochemical properties and transport across porous separators in nonaqueous solvents.

    Science.gov (United States)

    Nagarjuna, Gavvalapalli; Hui, Jingshu; Cheng, Kevin J; Lichtenstein, Timothy; Shen, Mei; Moore, Jeffrey S; Rodríguez-López, Joaquín

    2014-11-19

    Enhancing the ionic conductivity across the electrolyte separator in nonaqueous redox flow batteries (NRFBs) is essential for improving their performance and enabling their widespread utilization. Separating redox-active species by size exclusion without greatly impeding the transport of supporting electrolyte is a potentially powerful alternative to the use of poorly performing ion-exchange membranes. However, this strategy has not been explored possibly due to the lack of suitable redox-active species that are easily varied in size, remain highly soluble, and exhibit good electrochemical properties. Here we report the synthesis, electrochemical characterization, and transport properties of redox-active poly(vinylbenzyl ethylviologen) (RAPs) with molecular weights between 21 and 318 kDa. The RAPs reported here show very good solubility (up to at least 2.0 M) in acetonitrile and propylene carbonate. Ultramicroelectrode voltammetry reveals facile electron transfer with E1/2 ∼ -0.7 V vs Ag/Ag(+)(0.1 M) for the viologen 2+/+ reduction at concentrations as high as 1.0 M in acetonitrile. Controlled potential bulk electrolysis indicates that 94-99% of the nominal charge on different RAPs is accessible and that the electrolysis products are stable upon cycling. The dependence of the diffusion coefficient on molecular weight suggests the adequacy of the Stokes-Einstein formalism to describe RAPs. The size-selective transport properties of LiBF4 and RAPs across commercial off-the-shelf (COTS) separators such as Celgard 2400 and Celgard 2325 were tested. COTS porous separators show ca. 70 times higher selectivity for charge balancing ions (Li(+)BF4(-)) compared to high molecular weight RAPs. RAPs rejection across these separators showed a strong dependence on polymer molecular weight as well as the pore size; the rejection increased with both increasing polymer molecular weight and reduction in pore size. Significant rejection was observed even for rpoly/rpore (polymer

  2. Formation of Foam-like Microstructural Carbon Material by Carbonization of Porous Coordination Polymers through a Ligand-Assisted Foaming Process.

    Science.gov (United States)

    Kongpatpanich, Kanokwan; Horike, Satoshi; Fujiwara, Yu-Ichi; Ogiwara, Naoki; Nishihara, Hirotomo; Kitagawa, Susumu

    2015-09-14

    Porous carbon material with a foam-like microstructure has been synthesized by direct carbonization of porous coordination polymer (PCP). In situ generation of foaming agents by chemical reactions of ligands in PCP during carbonization provides a simple way to create lightweight carbon material with a foam-like microstructure. Among several substituents investigated, the nitro group has been shown to be the key to obtain the unique foam-like microstructure, which is due to the fast kinetics of gas evolution during carbonization. Foam-like microstructural carbon materials showed higher pore volume and specific capacitance compared to a microporous carbon.

  3. Grafting of molecularly imprinted polymer to porous polyethylene filtration membranes by plasma polymerization.

    Science.gov (United States)

    Cowieson, D; Piletska, E; Moczko, E; Piletsky, S

    2013-08-01

    An application of plasma-induced grafting of polyethylene membranes with a thin layer of molecularly imprinted polymer (MIP) was presented. High-density polyethylene (HDPE) membranes, "Vyon," were used as a substrate for plasma grafting modification. The herbicide atrazine, one of the most popular targets of the molecular imprinting, was chosen as a template. The parameters of the plasma treatment were optimized in order to achieve a good balance between polymerization and ablation processes. Modified HDPE membranes were characterized, and the presence of the grafted polymeric layer was confirmed based on the observed weight gain, pore size measurements, and infrared spectrometry. Since there was no significant change in the porosity of the modified membranes, it was assumed that only a thin layer of the polymer was introduced on the surface. The experiments on the re-binding of the template atrazine to the membranes modified with MIP and blank polymers were performed. HDPE membranes which were grafted with polymer using continuous plasma polymerization demonstrated the best result which was expressed in an imprinted factor equal to 3, suggesting that molecular imprinting was successfully achieved.

  4. Copper Capture in a Thioether-Functionalized Porous Polymer Applied to the Detection of Wilson's Disease.

    Science.gov (United States)

    Lee, Sumin; Barin, Gokhan; Ackerman, Cheri M; Muchenditsi, Abigael; Xu, Jun; Reimer, Jeffrey A; Lutsenko, Svetlana; Long, Jeffrey R; Chang, Christopher J

    2016-06-22

    Copper is an essential nutrient for life, but at the same time, hyperaccumulation of this redox-active metal in biological fluids and tissues is a hallmark of pathologies such as Wilson's and Menkes diseases, various neurodegenerative diseases, and toxic environmental exposure. Diseases characterized by copper hyperaccumulation are currently challenging to identify due to costly diagnostic tools that involve extensive technical workup. Motivated to create simple yet highly selective and sensitive diagnostic tools, we have initiated a program to develop new materials that can enable monitoring of copper levels in biological fluid samples without complex and expensive instrumentation. Herein, we report the design, synthesis, and properties of PAF-1-SMe, a robust three-dimensional porous aromatic framework (PAF) densely functionalized with thioether groups for selective capture and concentration of copper from biofluids as well as aqueous samples. PAF-1-SMe exhibits a high selectivity for copper over other biologically relevant metals, with a saturation capacity reaching over 600 mg/g. Moreover, the combination of PAF-1-SMe as a material for capture and concentration of copper from biological samples with 8-hydroxyquinoline as a colorimetric indicator affords a method for identifying aberrant elevations of copper in urine samples from mice with Wilson's disease and also tracing exogenously added copper in serum. This divide-and-conquer sensing strategy, where functional and robust porous materials serve as molecular recognition elements that can be used to capture and concentrate analytes in conjunction with molecular indicators for signal readouts, establishes a valuable starting point for the use of porous polymeric materials in noninvasive diagnostic applications.

  5. USE OF POROUS BIODEGRADABLE POLYMER IMPLANTS IN MENISCUS RECONSTRUCTION .1. PREPARATION OF POROUS BIODEGRADABLE POLYURETHANES FOR THE RECONSTRUCTION OF MENISCUS LESIONS

    NARCIS (Netherlands)

    DEGROOT, JH; NIJENHUIS, AJ; BRUIN, P; PENNINGS, AJ; VETH, RPH; JANSEN, HWB

    1990-01-01

    Porous biodegradable poly(urethanes) for reconstructing menisci have been prepared using two different combinations of techniques: freeze-drying/salt-leaching and in-situ polymerization/salt-leaching. Using these methods, homogenous porous materials with a controllable and reproducible morphology ca

  6. Preparation and characterization of a micro-porous polymer electrolyte with cross-linking network structure for dye-sensitized solar cell

    Energy Technology Data Exchange (ETDEWEB)

    Wei, T.C.; Wan, C.C.; Wang, Y.Y. [Department of Chemical Engineering, National Tsing-Hua University, 101, Section 2, Kuang Fu Road, Hsin-Chu 300 (China)

    2007-12-14

    A PVdF-HFP/PEG/PEGDMA cross-linking film has been prepared as the electrolyte for dye-sensitized solar cell (DSSC). The film can be made porous by controlling the evaporation behavior of solvents. Room temperature ionic conductivity of the micro-porous film exceeds 1 mS/cm. In addition, we also evaluated the significance of cell gap in DSSC by analyzing the impedance spectroscopy of the cell with polymer electrolyte. Finally, by decreasing the film thickness, the DSSC equipped with 11 {mu}m, micro-porous and cross-linked film showed a conversion efficiency over 4% and 5% under 1 and 0.16 Sun, respectively. (author)

  7. Nitrogen-doped biomass/polymer composite porous carbons for high performance supercapacitor

    Science.gov (United States)

    Shu, Yu; Maruyama, Jun; Iwasaki, Satoshi; Maruyama, Shohei; Shen, Yehua; Uyama, Hiroshi

    2017-10-01

    Nitrogen-doped porous monolithic carbon (NDPMC) is obtained from biomass-derived activated carbon/polyacrylonitrile composite for the first time via a template-free thermally induced phase separation (TIPS) approach followed by KOH activation. The electrochemical results indicate that NDPMC possesses ultrahigh specific capacitance of 442 F g-1 at 1 A g-1, excellent rate capability with 81% retention rate from 1 to 100 A g-1 and outstanding cycling stability with 98% capacitance retention at 20 A g-1 after 5000 cycles. Furthermore, the evaluation of NDPMC on the practical symmetrical system also exhibits desired electrochemical performances. The novel composite carbon displays remarkable capacitance properties and the feasible, low-cost synthetic route demonstrates great potential for large-scale production of high-performance electrode materials for supercapacitors.

  8. Polymer functionalized nanostructured porous silicon for selective water vapor sensing at room temperature

    Science.gov (United States)

    Dwivedi, Priyanka; Das, Samaresh; Dhanekar, Saakshi

    2017-04-01

    This paper highlights the surface treatment of porous silicon (PSi) for enhancing the sensitivity of water vapors at room temperature. A simple and low cost technique was used for fabrication and functionalization of PSi. Spin coated polyvinyl alcohol (PVA) was used for functionalizing PSi surface. Morphological and structural studies were conducted to analyze samples using SEM and XRD/Raman spectroscopy respectively. Contact angle measurements were performed for assessing the wettability of the surfaces. PSi and functionalized PSi samples were tested as sensors in presence of different analytes like ethanol, acetone, isopropyl alcohol (IPA) and water vapors in the range of 50-500 ppm. Electrical measurements were taken from parallel aluminium electrodes fabricated on the functionalized surface, using metal mask and thermal evaporation. Functionalized PSi sensors in comparison to non-functionalized sensors depicted selective and enhanced response to water vapor at room temperature. The results portray an efficient and selective water vapor detection at room temperature.

  9. High-Sensitivity and Low-Hysteresis Porous MIM-Type Capacitive Humidity Sensor Using Functional Polymer Mixed with TiO2 Microparticles

    Science.gov (United States)

    Liu, Ming-Qing; Wang, Cong; Kim, Nam-Young

    2017-01-01

    In this study, a high-sensitivity and low-hysteresis porous metal–insulator–metal-type capacitive humidity sensor is investigated using a functional polymer mixed with TiO2 microparticles. The humidity sensor consists of an optimally designed porous top electrode, a functional polymer humidity sensitive layer, a bottom electrode, and a glass substrate. The porous top electrode is designed to increase the contact area between the sensing layer and water vapor, leading to high sensitivity and quick response time. The functional polymer mixed with TiO2 microparticles shows excellent hysteresis under a wide humidity-sensing range with good long-term stability. The results show that as the relative humidity ranges from 10% RH to 90% RH, the proposed humidity sensor achieves a high sensitivity of 0.85 pF/% RH and a fast response time of less than 35 s. Furthermore, the sensor shows an ultra-low hysteresis of 0.95% RH at 60% RH, a good temperature dependence, and a stable capacitance value with a maximum of 0.17% RH drift during 120 h of continuous test. PMID:28157167

  10. Highly stable CO2/N2 and CO2/CH4 selectivity in hyper-cross-linked heterocyclic porous polymers.

    Science.gov (United States)

    Saleh, Muhammad; Lee, Han Myoung; Kemp, K Christian; Kim, Kwang S

    2014-05-28

    The largest obstacles for landfill/flue gas separation using microporous materials are small adsorption values and low selectivity ratios. This study demonstrates that these adsorption and selectivity challenges can be overcome by utilizing a series of hyper-cross-linked heterocyclic polymer networks. These microporous organic polymers (MOPs) were synthesized in a single step by inexpensive Friedel-Crafts-catalyzed reactions using dimethoxymethane as an external linker. The amorphous networks show moderate Brunauer-Emmett-Teller surface areas up to 1022 m(2) g(-1), a narrow pore size distribution in the range from 6 to 8 Å, and high physicochemical stability. Owing to the presence of the heteroatomic pore surfaces in the networks, they exhibit maximum storage capacities for CO2 of 11.4 wt % at 273 K and 1 atm. Additionally, remarkable selectivity ratios for CO2 adsorption over N2 (100) and CH4 (15) at 273 K were obtained. More importantly, as compared with any other porous materials, much higher selectivity for CO2/N2 (80) and CO2/CH4 (15) was observed at 298 K, showing that these selectivity ratios remain high at elevated temperature. The very high CO2/N2 selectivity values are ascribed to the binding affinity of abundantly available electron-rich basic heteroatoms, high CO2 isoteric heats of adsorption (49-38 kJ mol(-1)), and the predominantly microporous nature of the MOPs. Binding energies calculated using the high level of ab initio theory showed that the selectivity is indeed attributed to the heteroatom-CO2 interactions. By employing an easy and economical synthesis procedure these MOPs with high thermochemical stability are believed to be a promising candidate for selective CO2 capture.

  11. Studies of the influence of nonequilibrium plasma thermal exposure on the characteristics of the capillary-porous polymer material

    Science.gov (United States)

    Makhotkina, L. Yu; Khristoliubova, V. I.

    2017-01-01

    Capillary-porous materials, which include natural macromolecular tanning material, are exposed to a number of factors during the treatment by a nonequilibrium plasma. Plasma particles exchange the charge and energy with the atoms of the material during the interaction of the plasma with the surface. The results of treatment are desorption of atoms and molecules from the body surface, sputtering and evaporation of material’s particles, changes of the structure and phase state. In real terms during the modification of solids by nonequilibrium low-temperature plasma thermal effect influences the process. The energy supplied from the discharge during the process with low pressure, which is converted into heat, is significantly less than during the atmospheric pressure, but the thermal stability of high-molecular compounds used in the manufacture of materials and products of the tanning industry, is very limited and depends on the duration of the effect of temperature. Even short heating of hydrophilic polymers (proteins) (100-180 °C) causes a change in their properties. It decreases the collagen ability to absorb water vapor, to swell in water, acids, alkalis, and thus decreases their durability. Prolonged heating leads to a deterioration of the physical and mechanical properties. Higher heating temperatures it leads to the polymer degradation. The natural leather temperature during plasma exposure does not rise to a temperature of collagen degradation and does not result in changes of physical phase of the dermis. However, the thermal plasma exposure must be considered, since the high temperatures influence on physical and mechanical properties.

  12. The triazine-based porous organic polymer: Novel synthetic strategy for high specific surface area

    Energy Technology Data Exchange (ETDEWEB)

    Park, Jin Kuen [Dept. of Chemistry, Hankuk University of Foreign Studies, Yongin (Korea, Republic of)

    2017-02-15

    A new type of microporous polymer has been successively synthesized via a simple polycondensation reaction with the 2,4-diaminotriazine moiety and dianhydride monomer. Diaminotriazine moieties in M1 especially can provide effective branching sites, resulting in high surface areas up to 1150 m{sup 2} /g. In addition, the specific pore structure of the polyimide POP in its solid state can be modified by the surface activation method. Therefore, it can be expected that the resulting material will be a promising candidate for gas storage, and with this synthetic strategy, various type of derivatives will also be optimized.

  13. Hierarchical Porous Polymer Beads Prepared by Polymerization-induced Phase Separation and Emulsion-template in a Microfluidic Device

    Institute of Scientific and Technical Information of China (English)

    Wei-cai Wang; Yan-xiong Pan; Kai Shi; Chao Peng; Xiang-ling Ji

    2014-01-01

    Porous polymer beads (PPBs) containing hierarchical bimodal pore structure with gigapores and meso-macropores were prepared by polymerization-induced phase separation (PIPS) and emulsion-template technique in a glass capillary microfluidic device (GCMD).Fabrication procedure involved the preparation of water-in-oil emulsion by emulsifying aqueous solution into the monomer solution that contains porogen.The emulsion was added into the GCMD to fabricate the (water-in-oil)-in-water double emulsion droplets.The flow rate of the carrier continuous phase strongly influenced the formation mechanism and size of droplets.Formation mechanism transformed from dripping to jetting and size of droplets decreased from 550 μm to 250 μm with the increase in flow rate of the carrier continuous phase.The prepared droplets were initiated for polymerization by on-line UV-irradiation to form PPBs.The meso-macropores in these beads were generated by PIPS because of the presence ofporogen and gigapores obtained from the emulsion-template.The pore morphology and pore size distribution of the PPBs were investigated extensively by scanning electron microscopy and mercury intrusion porosimetry (MIP).New pore morphology was formed at the edge of the beads different from traditional theory because of different osmolarities between the water phase of the emulsion and the cartier continuous phase.The morphology and proportion of bimodal pore structure can be tuned by changing the kind and amount of porogen.

  14. Development of Molecularly Imprinted Polymer in Porous Film Format for Binding of Phenol and Alkylphenols from Water

    Directory of Open Access Journals (Sweden)

    Andriy O. Gryshchenko

    2014-01-01

    Full Text Available Molecularly imprinted polymers (MIPs were fabricated on glass slides with a “sandwich” technique giving ~20 µm thick films. Methanol/water as a solvent, and polyethyleneglycol and polyvinylacetate as solvent modifiers, were used to give a porous morphology, which was studied with scanning electron microscopy and gravimetric analysis. Various MIPs were synthesized through non-covalent imprinting with phenol as the template; itaconic acid, 4-vinylpyridine, and styrene as monomers; ethylene glycol dimethacrylate, triethylene glycol dimethacrylate, and pentaerythritol triacrylate (PETA as cross-linkers. Binding and imprinting properties of the MIPs were evaluated based on phenol adsorption isotherms. Since phenol has only one weakly acidic hydroxyl group and lacks unique structural characteristics necessary for binding specificity, the preparation of selective MIPs was challenging. The recognition of phenol via hydrogen bonding is suppressed in water, while hydrophobic interactions, though promoted, are not specific enough for highly-selective phenol recognition. Nevertheless, the styrene-PETA MIP gave modest imprinting effects, which were higher at lower concentrations (Imprinting Factor (IF = 1.16 at 0.5 mg·L−1. The isotherm was of a Freundlich type over 0.1–40 mg·L−1 and there was broad cross-reactivity towards other structurally similar phenols. This shows that phenol MIPs or simple adsorbents can be developed based on styrene for hydrophobic binding, and PETA to form a tighter, hydrophilic network.

  15. Syntheses, crystal structures, and water adsorption behaviors of jungle-gym-type porous coordination polymers containing nitro moieties

    Science.gov (United States)

    Uemura, Kazuhiro; Onishi, Fumiaki; Yamasaki, Yukari; Kita, Hidetoshi

    2009-10-01

    NO 2 containing dicarboxylate bridging ligands, nitroterephthalate (bdc-NO 2) and 2,5-dinitroterephthalate (bdc-(NO 2) 2), afford porous coordination polymers, {[Zn 2(bdc-NO 2) 2(dabco)]· solvents} n ( 2⊃ solvents) and {[Zn 2(bdc-(NO 2) 2) 2(dabco)]· solvents} n ( 3⊃ solvents). Both compounds form jungle-gym-type regularities, where a 2D square grid composed of dinuclear Zn 2 units and dicarboxylate ligands is bridged by dabco molecules to extend the 2D layers into a 3D structure. In 2⊃ solvents and 3⊃ solvents, a rectangle pore surrounded by eight Zn 2 corners contains two and four NO 2 moieties, respectively. Thermal gravimetry (TG) and X-ray powder diffraction (XRPD) measurements reveal that both compounds maintain the frameworks regularities without guest molecules and with solvents such as MeOH, EtOH, i-PrOH, and Me 2CO. Adsorption measurements reveal that dried 2 and 3 adsorb H 2O molecules to be {[Zn 2(bdc-NO 2) 2(dabco)]·4H 2O} n ( 2⊃4H 2O) and {[Zn 2(bdc-(NO 2) 2) 2(dabco)]·6H 2O} n ( 3⊃6H 2O), showing the pore hydrophilicity enhancement caused by NO 2 group introduction.

  16. Eliminating micro-porous layer from gas diffusion electrode for use in high temperature polymer electrolyte membrane fuel cell

    Science.gov (United States)

    Su, Huaneng; Xu, Qian; Chong, Junjie; Li, Huaming; Sita, Cordellia; Pasupathi, Sivakumar

    2017-02-01

    In this work, we report a simple strategy to improve the performance of high temperature polymer electrolyte membrane fuel cell (HT-PEMFC) by eliminating the micro-porous layer (MPL) from its gas diffusion electrodes (GDEs). Due to the absence of liquid water and the general use of high amount of catalyst, the MPL in a HT-PEMFC system works limitedly. Contrarily, the elimination of the MPL leads to an interlaced micropore/macropore composited structure in the catalyst layer (CL), which favors gas transport and catalyst utilization, resulting in a greatly improved single cell performance. At the normal working voltage (0.6 V), the current density of the GDE eliminated MPL reaches 0.29 A cm-2, and a maximum power density of 0.54 W cm-2 at 0.36 V is obtained, which are comparable to the best results yet reported for the HT-PEMFCs with similar Pt loading and operated using air. Furthermore, the MPL-free GDE maintains an excellent durability during a preliminary 1400 h HT-PEMFC operation, owing to its structure advantages, indicating the feasibility of this electrode for practical applications.

  17. Integration of porous coordination polymers and gold nanorods into core-shell mesoscopic composites toward light-induced molecular release.

    Science.gov (United States)

    Khaletskaya, Kira; Reboul, Julien; Meilikhov, Mikhail; Nakahama, Masashi; Diring, Stéphane; Tsujimoto, Masahiko; Isoda, Seiji; Kim, Franklin; Kamei, Ken-ichiro; Fischer, Roland A; Kitagawa, Susumu; Furukawa, Shuhei

    2013-07-31

    Besides conventional approaches for regulating in-coming molecules for gas storage, separation, or molecular sensing, the control of molecular release from the pores is a prerequisite for extending the range of their application, such as drug delivery. Herein, we report the fabrication of a new porous coordination polymer (PCP)-based composite consisting of a gold nanorod (GNR) used as an optical switch and PCP crystals for controlled molecular release using light irradiation as an external trigger. The delicate core-shell structures of this new platform, composed of an individual GNR core and an aluminum-based PCP shell, were achieved by the selective deposition of an aluminum precursor onto the surface of GNR followed by the replication of the precursor into aluminum-based PCPs. The mesoscopic structure was characterized by electron microscopy, energy dispersive X-ray elemental mapping, and sorption experiments. Combination at the nanoscale of the high storage capacity of PCPs with the photothermal properties of GNRs resulted in the implementation of unique motion-induced molecular release, triggered by the highly efficient conversion of optical energy into heat that occurs when the GNRs are irradiated into their plasmon band. Temporal control of the molecular release was demonstrated with anthracene as a guest molecule and fluorescent probe by means of fluorescence spectroscopy.

  18. Porous organic polymer/RGO composite as high performance cathode for half and full sodium ion batteries

    Science.gov (United States)

    Li, Aihua; Feng, Zhenyu; Sun, Yan; Shang, Limei; Xu, Liqiang

    2017-03-01

    Redox-active organic polymers are promising cathode electrodes owing to the advantages of open and flexible frame-works, renewability and environmental friendliness. Sodium salt of poly (2, 5-dihydroxy-p-benzoquinonyl sulfide)/RGO (Na2PDHBQS/RGO) composite has been fabricated via a convenient route and applied as a high performance and stable cathode for sodium ion batteries. The Na2PDHBQS/RGO was investigated in ether-based electrolyte, which demonstrated better electrochemical performances (228, 214, 203, 193, 172 and 147 mAh g-1 at 0.1, 0.2, 0.4, 0.8, 2 and 4C, respectively) than that in traditional ester-based ones. The high specific capacity, excellent cycle stability and reversibility of Na2PDHBQS/RGO may be attributed to the special porous structure, enhanced electronic conductivity by the introduction of RGO and fast sodium ion and electron diffusion rate in ether-based electrolyte. In addition, the Na2PDHBQS/RGO cathode has been assembled with disodium terephthalate (Na2TP) anode to compose a full cell for the first time, which presents an initial reversible capacity of 210 mAh g-1 at 0.1C.

  19. A 3D porous polymer monolith-based platform integrated in poly(dimethylsiloxane) microchips for immunoassay.

    Science.gov (United States)

    Kang, Qin-Shu; Shen, Xiao-Fan; Hu, Na-Na; Hu, Meng-Jia; Liao, Hui; Wang, Han-Zhong; He, Zhi-Ke; Huang, Wei-Hua

    2013-05-01

    In this work, we demonstrate the immunocapture and on-line fluorescence immunoassay of protein and virus based on porous polymer monoliths (PPM) in microfluidic devices. Poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate) [poly(GMA-co-EGDMA)] monoliths were successfully synthesized in the polydimethylsiloxane (PDMS) microfluidic channels by in situ UV-initiated free radical polymerization. After surface modification, PPM provides a high-surface area and specific affinity 3D substrate for immunoassays. Combining with well controlled microfluidic devices, the direct immunoassay of IgG and sandwich immunoassay of inactivated H1N1 influenza virus using 5 μL sample has been accomplished, with detection limits of 4 ng mL(-1) and less than 10 pg mL(-1), respectively. The enhanced detection sensitivity is due to both high surface area of PPM and flow-through design. The detection time was obviously decreased mainly due to the shortened diffusion distance and improved convective mass transfer inside the monolith, which accelerates the reaction kinetics between antigen and antibody. This work provides a novel microfluidic immunoassay platform with high efficiency thereby enabling fast and sensitive immunoassay.

  20. The Paramagnetic 2D Chiral-porous Polymer of L-Phenylalanine and Manganese

    Institute of Scientific and Technical Information of China (English)

    翁家宝; 洪茂椿; 曹荣; 时茜; 陈新滋

    2003-01-01

    [Mn(L-Phe)2@ H2O]n (Phe=phenylalanine) with a single stranded coordination polymer has been synthesized by self-assembly of manganese salt and phenylalanine and characterized by X-ray single-crystal diffraction method. The complex crystallizes in the orthorhombic, space group P212121 with a = 6.0911(1), b = 10.3642(1), c = 30.4321(7) A, V= 1921.16(6) A3, Z= 4, Dc= 1.387 g/cm3, C18H22N2O5Mn, Mr = 401.32, F(000) = 836 and μ(MoKoα) = 0.717 mm-1. The final R = 0.0614 and wR = 0.1412 for 2291 observed reflections with L> 2σ(I). The magnetic behavior study shows that there exist super-exchange antiferromagnetic interactions between the magnetic centers through the effective exchange pathway of the carboxylate group.

  1. Molecularly imprinted polymer grafted to porous polyethylene frits: a new selective solid-phase extraction format.

    Science.gov (United States)

    Barahona, Francisco; Turiel, Esther; Martín-Esteban, Antonio

    2011-10-07

    In this paper, a novel format for selective solid-phase extraction based on a molecularly imprinted polymer (MIP) is described. A small amount of MIP has been synthesized within the pores of commercial polyethylene (PE) frits and attached to its surface using benzophenone (BP), a photo-initiator capable to start the polymerisation from the surface of the support material. Key properties affecting the obtainment of a proper polymeric layer, such as polymerisation time and kind of cross-linker were optimised. The developed imprinted material has been applied as a selective sorbent for cleaning extracts of thiabendazole (TBZ), as model compound, from citrus samples. The use of different solvents for loading the analyte in the imprinted frits was investigated, as well as the binding capacity of the imprinted polymer. Imprinted frits showed good selectivity when loads were performed using toluene and a linear relationship was obtained for the target analyte up to 1000 ng of loaded analyte. Prepared composite material was applied to the SPE of TBZ in real samples extracts, showing an impressive clean-up ability. Calibrations showed good linearity in the concentration range of 0.05-5.00 μg g(-1), referred to the original solid sample, and the regression coefficients obtained were greater than 0.996. The calculated detection limit was 0.016 μg g(-1), low enough to satisfactory analysis of TBZ in real samples. RSDs at different spiking levels ranged below 15% in all the cases and imprinted frits were reusable without loss in their performance.

  2. Development of Porous Polymers via Pickering HIPEs Template%Pickering HIPEs 模板构建多孔聚合物的研究进展

    Institute of Scientific and Technical Information of China (English)

    陈香; 潘建明; 闫永胜

    2016-01-01

    对近年来Pickering ( high internal phase emulsions , HIPEs )模板法制备多孔聚合物的工作进行了总结,阐述了Pickering HIPEs模板的形成机理和影响稳定性的因素,介绍了多孔材料( PolyHIPEs )的形貌控制和改性的有效手段,初步探讨了PolyHIPEs的应用现状和前景。 Pickering HIPEs模板法具有乳液稳定性好、形成过程环境友好、获得的多孔聚合物孔结构易控制等优点,有望应用于工业催化、能源转化、生物医学和化工分离等领域。%The porous polymers via Pickering HIPEs template were studied .The formation mechanism of Pickering HIPEs template and effects to the stability of template were discussed .The methods for controlling the porous structure and modification were demonstrated.Finally, the application status and prospect of porous polymers resulted from Pickering HIPEs template were also introduced .Pickering HIPEs possessed the advantages of stable emulsion , environment-friendly formation process , easy controlled the structure of as-prepared porous polymers.Thus, Pickering HIPEs had the potential to the fields of industrial catalysis , energy conversion , biomedicine and chemical separation .

  3. A key factor in modern protection of historic buildings: the assessment of penetration of water-repellent polymers into porous stone-materials.

    Science.gov (United States)

    Toniolo, L; Casadio, F; Cariati, F

    2001-01-01

    From the 1960s on, the conservation of monuments and stone masonry has witnessed an increasing use of polymeric products during restoration interventions. Actual penetration depths reached by different polymers within the porous stone matrix are supposed to be key factors in determining the efficacy of the treatments themselves (besides, of course, the chemical-mineralogical nature of the stone and the chemical-physical characteristics of the various polymers). This work presents some preliminary results obtained on specimens of Noto calcarenite treated with various polymeric protective products. Samples were investigated with direct analytical methods (micro-ATR spectroscopy, SEM) in order to assess penetration depths reached by polymers inside the stone while reducing to a minimum the necessary manipulation of specimens. The obtained results highlighted the following trend in penetration depths for the various products tested: siloxane product > partially fluorinated acrylic resin > acrylic resin. Moreover, data obtained allowed to establish direct correlation between long term efficacy of products and relative penetration depths.

  4. Selective Ag(I) binding, H2S sensing, and white-light emission from an easy-to-make porous conjugated polymer.

    Science.gov (United States)

    Liu, Jie; Yee, Ka-Kit; Lo, Kenneth Kam-Wing; Zhang, Kenneth Yin; To, Wai-Pong; Che, Chi-Ming; Xu, Zhengtao

    2014-02-19

    Separating silver (Ag(+)) from lead (Pb(2+)) is one of the many merits of the porous polymer framework reported here. The selective metal binding stems from the well-defined chelating unit of N-heterocycles, which consists of a triazine (C3N3) ring bonded to three 3,5-dimethylpyrazole moieties. Such a rigid and open triad also serves as the distinct building unit in the fully conjugated 3D polymer scaffold. Because of its strong fluorescence and porosity (e.g., BET surface area: 355 m(2)/g), and because of the various types of metal species that can be readily taken up, this versatile framework is especially fit for functionalization. For example, with AgNO3 loaded, the framework solid exhibits a brown color in response to water solutions of H2S, even at the dilution of 5.0 μM (0.17 ppm); whereas cysteine and other biologically relevant thiols do not cause notable change in color. In another example, tunable white-light emission was produced when an Ir(III) complex was doped (e.g., about 0.02% of the polymer weight) onto the framework. Mechanistically, the bound Ir(III) centers become highly emissive in the orange-red region, complementing the broad, bluish emission from the polymer host to result in the overall white-light quality: the color attributes of the emission are therefore easily tunable by the Ir(III) dopant concentration. With this exemplary study, we intend to highlight metal uptake as an effective approach to modify and enrich the properties of porous polymer frameworks and to stimulate interest in further examining metal-polymer interactions in the context of sensing, separation, catalyzes, and other applications.

  5. Modeling Polymer Stabilized Nano-scale Zero Valent Iron Transport Experiments in Porous Media to Understand the Transport Behavior

    Science.gov (United States)

    Mondal, P.; Krol, M.; Sleep, B. E.

    2015-12-01

    A wide variety of groundwater contaminants can be treated with nano-scale zero valent iron (nZVI). However, delivery of nZVI in the subsurface to the treatment zones is challenging as the bare nZVI particles have a higher tendency to agglomerate. The subsurface mobility of nZVI can be enhanced by stabilizing nZVI with polymer, such as carboxymethyl cellulose (CMC). In this study, numerical simulations were conducted to evaluate CMC stabilized nZVI transport behavior in porous media. The numerical simulations were based on a set of laboratory-scale transport experiments that were conducted in a two-dimensional water-saturated glass-walled sandbox (length - 55 cm; height - 45 cm; width - 1.4 cm), uniformly packed with silica sand. In the transport experiments: CMC stabilized nZVI and a non-reactive dye tracer Lissamine Green B (LGB) were used; water specific discharge and CMC concentration were varied; movements of LGB, and CMC-nZVI in the sandbox were tracked using a camera, a light source and a dark box. The concentrations of LGB, CMC, and CMC-nZVI at the sandbox outlet were analyzed. A 2D multiphase flow and transport model was applied to simulate experimental results. The images from LGB dye transport experiments were used to determine the pore water velocities and media permeabilities in various layers in the sand box. These permeability values were used in the subsequent simulations of CMC-nZVI transport. The 2D compositional simulator, modified to include colloid filtration theory (CFT), treated CMC as a solute and nZVI as a colloid. The simulator included composition dependent viscosity to account for CMC injection and mixing, and attachment efficiency as a fitting parameter for nZVI transport modeling. In the experiments, LGB and CMC recoveries were greater than 95%; however, CMC residence time was significantly higher than the LGB residence time and the higher CMC concentration caused higher pressure drops in the sandbox. The nZVI recovery was lower than 40

  6. Ultrathin, freestanding, stimuli-responsive, porous membranes from polymer hydrogel-brushes

    Science.gov (United States)

    Kang, Chengjun; Ramakrishna, Shivaprakash N.; Nelson, Adrienne; Cremmel, Clement V. M.; Vom Stein, Helena; Spencer, Nicholas D.; Isa, Lucio; Benetti, Edmondo M.

    2015-07-01

    The fabrication of freestanding, sub-100 nm-thick, pH-responsive hydrogel membranes with controlled nano-morphology, based on modified poly(hydroxyethyl methacrylate) (PHEMA) is presented. Polymer hydrogel-brush films were first synthesized by surface-initiated atom transfer radical polymerization (SI-ATRP) and subsequently detached from silicon substrates by UV-induced photo-cleavage of a specially designed linker within the initiator groups. The detachment was also assisted by pH-induced osmotic forces generated within the films in the swollen state. The mechanical properties and morphology of the freestanding films were studied by atomic force microscopy (AFM). Inclusion of nanopores of controlled diameter was accomplished by performing SI-ATRP from initiator-coated surfaces that had previously been patterned with polystyrene nanoparticles. Assembly parameters and particle sizes could be varied, in order to fabricate nanoporous hydrogel-brush membranes with tunable pore coverage and characteristics. Additionally, due to the presence of weak polyacid functions within the hydrogel, the membranes exhibited pH-dependent thickness in water and reversible opening/closing of the pores.The fabrication of freestanding, sub-100 nm-thick, pH-responsive hydrogel membranes with controlled nano-morphology, based on modified poly(hydroxyethyl methacrylate) (PHEMA) is presented. Polymer hydrogel-brush films were first synthesized by surface-initiated atom transfer radical polymerization (SI-ATRP) and subsequently detached from silicon substrates by UV-induced photo-cleavage of a specially designed linker within the initiator groups. The detachment was also assisted by pH-induced osmotic forces generated within the films in the swollen state. The mechanical properties and morphology of the freestanding films were studied by atomic force microscopy (AFM). Inclusion of nanopores of controlled diameter was accomplished by performing SI-ATRP from initiator-coated surfaces that had

  7. 3D-printed silicate porous bioceramics using a non-sacrificial preceramic polymer binder.

    Science.gov (United States)

    Zocca, A; Elsayed, H; Bernardo, E; Gomes, C M; Lopez-Heredia, M A; Knabe, C; Colombo, P; Günster, J

    2015-05-22

    Silicate bioceramics possess an excellent bioactivity; however, shaping them into complex geometries is still challenging. Therefore, this paper aims to present a new strategy for the shaping of a bioglass-ceramic with controlled geometry and properties starting from a glass powder combined with a preceramic polymer, i.e. a silicon resin, and reactive fillers. The powder-based three-dimensional (3D)-printing of wollastonite (CaSiO3)-based silicate bioceramic parts was demonstrated in this work. The resin plays a dual role, as it not only acts as a non-sacrificial binder for the filler powders in the printing process but it also reacts with the fillers to generate the desired bioceramic phases. The mechanical and physical properties, i.e. ball-on-three-balls test, density, porosity and morphology, were evaluated in 3D-printed discs. These samples possessed a total porosity around 64 vol% and a biaxial flexural strength around 6 MPa. The raw materials used in this work also enabled the 3D-printing of scaffolds possessing a designed multi-scale porosity, suitable bioceramic phase assemblage and a compressive strength of 1 MPa (for cylindrical scaffolds with total porosity ~80 vol%). Solubility in TRIS/HCl and in vitro assays, i.e. viability, cytotoxicity and apoptosis assays, were also performed. In vitro tests indicated good cell viability and no cytotoxicity effect on the cells.

  8. Liquid water transport characteristics of porous diffusion media in polymer electrolyte membrane fuel cells: A review

    Science.gov (United States)

    Liu, Xunliang; Peng, Fangyuan; Lou, Guofeng; Wen, Zhi

    2015-12-01

    Fundamental understanding of liquid water transport in gas diffusion media (GDM) is important to improve the material and structure design of polymer electrolyte membrane (PEM) fuel cells. Continuum methods of two-phase flow modeling facilitate to give more details of relevant information. The proper empirical correlations of liquid water transport properties, such as capillary characteristics, water relative permeability and effective contact angle, are crucial to two phase flow modeling and cell performance prediction. In this work, researches on these properties in the last decade are reviewed. Various efforts have been devoted to determine the water transport properties for GDMs. However, most of the experimental studies are ex-situ measurements. In-situ measurements for GDMs and extending techniques available to study the catalyst layer and the microporous layer will be further challenges. Using the Leverett-Udell correlation is not recommended for quantitative modeling. The reliable Leverett-type correlation for GDMs, with the inclusion of the cosine of effective contact angle, is desirable but hard to be established for modeling two-phase flow in GDMs. A comprehensive data set of liquid water transport properties is needed for various GDM materials under different PEM fuel cell operating conditions.

  9. Porous nitrogen doped carbon fiber with churros morphology derived from electrospun bicomponent polymer as highly efficient electrocatalyst for Zn-air batteries

    Science.gov (United States)

    Park, Gi Su; Lee, Jang-Soo; Kim, Sun Tai; Park, Soojin; Cho, Jaephil

    2013-12-01

    Highly porous nitrogen doped carbon fibers like churros morphology are prepared from a simple and cost-effective fabrication process, electrospinning with bicomponent polymer consisting of polystyrene (PS) and polyacrylonitrile (PAN). From appropriate ratio of two polymer and pyrolysis at 1100 °C, newly churros morphology with extremely high surface area (1271 m2 g-1) is prepared. During carbonization, more unstable PS than PAN plays a critical role in forming such morphology by acting as sacrifice materials, thus providing additional formation of inner pores and outer etched surfaces. Furthermore, it demonstrates excellent electrocatalytic activity toward ORR, which is attributed to highly meso- and macro porous nitrogen-doped large surface area and enhanced graphitic-nitrogen groups of carbon fibers. For example, the performance of a Zn-air cell based on the nitrogen-doped porous carbon nanofibers exhibits a peak power density of 194 mW cm-2, comparable to that based on a commercial Pt/C catalyst (192 mW cm-2). Further, the generation of hydrogen peroxide ions (<20%) in a half cell is similar to that on the commercial Pt/C catalyst.

  10. Magnetic porous β-cyclodextrin polymer for magnetic solid-phase extraction of microcystins from environmental water samples.

    Science.gov (United States)

    Zhang, Wenmin; Lin, Mingxia; Wang, Meili; Tong, Ping; Lu, Qiaomei; Zhang, Lan

    2017-06-23

    Microcystins (MCs) are cyclic heptapeptide toxins and tumor promoters produced by cyanobacteria, which threaten the health of humans. In this study, magnetic porous β-cyclodextrin polymer (Fe3O4@SiO2@P-CDP) was synthesized and characterized by transmission electron microscopy, scanning electron microscopy, energy dispersive X-ray spectrometry, Fourier transform infrared spectrometry, X-ray diffraction, nitrogen adsorption porosimetry and vibrating sample magnetometer. The synthesized Fe3O4@SiO2@P-CDP particles were then used for magnetic solid-phase extraction (MSPE) of MCs from environmental water samples, and exhibited excellent extraction performance, especially for MC-RR. Coupled with high-performance liquid chromatography with tandem mass spectrometry (HPLC-MS/MS), a simple, efficient and sensitive method for determination of trace levels of MCs was established. After the optimization of conditions, wide linear ranges (2.0-1000pgmL(-1)), good linearity (r(2)≥0.9996) and acceptable repeatability (RSD≤9.4%, n=5) were obtained. The limits of detection (LODs, S/N=3) and limits of quantification (LOQs, S/N=10) for three MCs (MC-LR, MC-RR and MC-YR) were in the range of 1.0-2.0pgmL(-1) and 2.0-5.0pgmL(-1), respectively. Typical water samples were analyzed by the developed method, and trace levels of MC-LR and MC-RR were detected. The results demonstrate that the developed method has great potential for the determination of MCs in complicated matrix. Copyright © 2017 Elsevier B.V. All rights reserved.

  11. Porous polymer scaffold for on-site delivery of stem cells--Protects from oxidative stress and potentiates wound tissue repair.

    Science.gov (United States)

    Geesala, Ramasatyaveni; Bar, Nimai; Dhoke, Neha R; Basak, Pratyay; Das, Amitava

    2016-01-01

    Wound healing by cell transplantation techniques often suffer setbacks due to oxidative stress encountered at injury sites. A porous polyethyleneglycol-polyurethane (PEG-PU) scaffold that facilitates cell delivery and boosts tissue repair was developed through semi-interpenetrating polymer network approach. The key physico-chemical properties assessed confirms these polymeric matrices are highly thermostable, barostable, degrade at an acidic pH (5.8), biodegradable, cytocompatible and possess excellent porosity. Mechanism of cellular penetration into porous polymer networks was evident by a ≥6 - fold increase in gene expression of MMP-13 and MMP-2 via activation of Akt and Erk. H2O2-induced apoptosis of mouse bone marrow stem cells (BMSCs) was abrogated in presence of polymer networks indicating a protective effect from oxidative stress. Transplantation of BMSC + PEG-PU at murine excisional splint wound site depicted significant increase in fibroblast proliferation, collagen deposition, anti-oxidant enzyme activities of catalase, SOD and GPx. Furthermore it significantly decreased expression of pro-inflammatory cytokines (IL-1β, TNF-α, IL-8, etc) with a concomitant increase in anti-inflammatory cytokines (IL-10, IL-13) at an early healing period of day 7. Finally, immunostaining revealed an enhanced engraftment and vascularity indicating an accelerated wound tissue closure. This pre-clinical study demonstrates the proof-of-concept and further necessitates their clinical evaluation as potential cell delivery vehicle scaffolds.

  12. Functionalization of alkyne-terminated thermally hydrocarbonized porous silicon nanoparticles with targeting peptides and antifouling polymers: effect on the human plasma protein adsorption.

    Science.gov (United States)

    Wang, Chang-Fang; Mäkilä, Ermei M; Bonduelle, Colin; Rytkönen, Jussi; Raula, Janne; Almeida, Sérgio; Närvänen, Ale; Salonen, Jarno J; Lecommandoux, Sebastien; Hirvonen, Jouni T; Santos, Hélder A

    2015-01-28

    Porous silicon (PSi) nanomaterials combine a high drug loading capacity and tunable surface chemistry with various surface modifications to meet the requirements for biomedical applications. In this work, alkyne-terminated thermally hydrocarbonized porous silicon (THCPSi) nanoparticles were fabricated and postmodified using five bioactive molecules (targeting peptides and antifouling polymers) via a single-step click chemistry to modulate the bioactivity of the THCPSi nanoparticles, such as enhancing the cellular uptake and reducing the plasma protein association. The size of the nanoparticles after modification was increased from 176 to 180-220 nm. Dextran 40 kDa modified THCPSi nanoparticles showed the highest stability in aqueous buffer. Both peptide- and polymer-functionalized THCPSi nanoparticles showed an extensive cellular uptake which was dependent on the functionalized moieties presented on the surface of the nanoparticles. The plasma protein adsorption study showed that the surface modification with different peptides or polymers induced different protein association profiles. Dextran 40 kDa functionalized THCPSi nanoparticles presented the least protein association. Overall, these results demonstrate that the "click" conjugation of the biomolecules onto the alkyne-terminated THCPSi nanoparticles is a versatile and simple approach to modulate the surface chemistry, which has high potential for biomedical applications.

  13. Hydrogen-bonded porous coordination polymers: structural transformation, sorption properties, and particle size from kinetic studies.

    Science.gov (United States)

    Uemura, Kazuhiro; Saito, Kazuya; Kitagawa, Susumu; Kita, Hidetoshi

    2006-12-20

    Three new coordination polymers, [CoCl2(4-pmna)2]n (1), {[Co(NCS)2(4-pmna)2].2Me2CO}n (2 superset 2Me2CO), and {[Co(4-pmna)2(H2O)2](NO3)2.2CH3OH}n (3 superset 2H2O.2MeOH) (4-pmna = N-(pyridin-4-ylmethyl)nicotinamide), have been synthesized and characterized using single-crystal X-ray diffraction. The cobalt(II) atoms are bridged by 4-pmna ligands in all three compounds to form double-stranded one-dimensional "repeated rhomboid-type" chains with rectangular-shaped cavities. In 1, each chain slips and obstructs the neighboring cavities so that there are no guest-incorporated pores. Both 2 superset 2Me2CO and 3 superset 2H2O.2MeOH do not have such a staggered arrangement and have pores that can be filled with a guest molecule. Compound 3 superset 2H2O.2MeOH traps guest molecules with multiple hydrogen bonds and shows a reversible structural rearrangement during adsorption and desorption. The new crystalline compound, 3, is stabilized by forming hydrogen bonds with the amide moieties of the 4-pmna ligands and was characterized using infrared spectroscopy. The clathration enthalpy of the reaction 3 + 2H2O(l) + 2MeOH(l) 3 superset 2H2O.2MeOH (approximately 35 kJ/mol) was estimated from differential scanning calorimetry data by considering the vaporization enthalpies of H2O and MeOH. The desorption process of 3 superset 2H2O.2MeOH --> 3 follows a single zero-order reaction mechanism under isothermal conditions. The activation energy of ca. 100 kJ/mol was obtained by plotting the logarithm of the reaction time for the same reacted fraction versus the reciprocal of the temperature. Moreover, the distribution of the one-dimensional channels in 3 superset 2H2O.2MeOH was estimated using the observation that the reaction rate is directly proportional to the total sectional area.

  14. Design of superhydrophobic porous coordination polymers through the introduction of external surface corrugation by the use of an aromatic hydrocarbon building unit.

    Science.gov (United States)

    Rao, Koya Prabhakara; Higuchi, Masakazu; Sumida, Kenji; Furukawa, Shuhei; Duan, Jingui; Kitagawa, Susumu

    2014-07-28

    We demonstrate a new approach to superhydrophobic porous coordination polymers by incorporating an anisotropic crystal morphology featuring a predominant surface that is highly corrugated and terminated by aromatic hydrocarbon moieties. The resulting low-energy surface provides particularly promising hydrophobic properties without the need for postsynthetic modifications or surface processing that would block the porosity of the framework. Consequently, hydrophobic organic molecules and water vapor are able to penetrate the surface and be densely accommodated within the pores, whereas bulk water is repelled as a result of the exterior surface corrugation derived from the aromatic surface groups. This study provides a new strategy for the design and development of superhydrophobic porous materials. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. One-pot synthesis of N-methylimidazolium-based porous polymer monolith for capillary electrochromatography via free radical copolymerization and quaterisation.

    Science.gov (United States)

    Li, Yi; Chen, Yingzhuang; Wang, Keyi; Nie, Lihua; Yao, Shouzhuo

    2012-07-01

    One-pot synthesis of porous polymer monolith decorated with N-methylimidazolium in a capillary was described. The polymer matrix was synthesized by in situ copolymerization and quaterization of 3-chloro-2-hydroxylpropyl methacrylate (CHPMA), ethylene dimethacrylate (EDMA), and N-methylimidazole (N-MIz). The influencing factors including amount of cross-linkers, composition of porogenic solvents, and polymerization temperature on the formation of the monolithic column were investigated. The monolithic column exhibited high column efficiency for thiourea, up to 135 000 plates per meter, and phenylmethanol, up to 102 000 plates per meter. Different types of compounds including alkylbenzenes, phenols, and inorganic anions were successfully baseline separated by capillary electrochromatography (CEC). The separation of theses analytes on the column indicated typical reversed-phase and anion-exchange chromatographic retention mechanism.

  16. Flows of Carreau fluid with pressure dependent viscosity in a variable porous medium: Application of polymer melt

    Directory of Open Access Journals (Sweden)

    M.Y. Malik

    2014-06-01

    Full Text Available The present work concerns the pressure dependent viscosity in Carreau fluid through porous medium. Four different combinations of pressure dependent viscosity and pressure dependent porous medium parameters are considered for two types of flow situations namely (i Poiseuille flow and (ii Couette flow. The solutions of non-linear equations have been evaluated numerically by Shooting method along with Runge-Kutta Fehlberg method. The physical features of pertinent parameters have been discussed through graphs.

  17. Porous polymer monolithic col

    Directory of Open Access Journals (Sweden)

    Lydia Terborg

    2015-05-01

    Full Text Available A new approach has been developed for the preparation of mixed-mode stationary phases to separate proteins. The pore surface of monolithic poly(glycidyl methacrylate-co-ethylene dimethacrylate capillary columns was functionalized with thiols and coated with gold nanoparticles. The final mixed mode surface chemistry was formed by attaching, in a single step, alkanethiols, mercaptoalkanoic acids, and their mixtures on the free surface of attached gold nanoparticles. Use of these mixtures allowed fine tuning of the hydrophobic/hydrophilic balance. The amount of attached gold nanoparticles according to thermal gravimetric analysis was 44.8 wt.%. This value together with results of frontal elution enabled calculation of surface coverage with the alkanethiol and mercaptoalkanoic acid ligands. Interestingly, alkanethiols coverage in a range of 4.46–4.51 molecules/nm2 significantly exceeded that of mercaptoalkanoic acids with 2.39–2.45 molecules/nm2. The mixed mode character of these monolithic stationary phases was for the first time demonstrated in the separations of proteins that could be achieved in the same column using gradient elution conditions typical of reverse phase (using gradient of acetonitrile in water and ion exchange chromatographic modes (applying gradient of salt in water, respectively.

  18. Cation-Dependent Stabilization of Electrogenerated Naphthalene Diimide Dianions in Porous Polymer Thin Films and Their Application to Electrical Energy Storage.

    Science.gov (United States)

    DeBlase, Catherine R; Hernández-Burgos, Kenneth; Rotter, Julian M; Fortman, David J; Abreu, Dieric dos S; Timm, Ronaldo A; Diógenes, Izaura C N; Kubota, Lauro T; Abruña, Héctor D; Dichtel, William R

    2015-11-02

    Porous polymer networks (PPNs) are attractive materials for capacitive energy storage because they offer high surface areas for increased double-layer capacitance, open structures for rapid ion transport, and redox-active moieties that enable faradaic (pseudocapacitive) energy storage. Here we demonstrate a new attractive feature of PPNs--the ability of their reduced forms (radical anions and dianions) to interact with small radii cations through synergistic interactions arising from densely packed redox-active groups, only when prepared as thin films. When naphthalene diimides (NDIs) are incorporated into PPN films, the carbonyl groups of adjacent, electrochemically generated, NDI radical anions and dianions bind strongly to K(+), Li(+), and Mg(2+), shifting the formal potentials of NDI's second reduction by 120 and 460 mV for K(+) and Li(+)-based electrolytes, respectively. In the case of Mg(2+), NDI's two redox waves coalesce into a single two-electron process with shifts of 240 and 710 mV, for the first and second reductions, respectively, increasing the energy density by over 20 % without changing the polymer backbone. In contrast, the formal reduction potentials of NDI derivatives in solution are identical for each electrolyte, and this effect has not been reported for NDI previously. This study illustrates the profound influence of the solid-state structure of a polymer on its electrochemical response, which does not simply reflect the solution-phase redox behavior of its monomers.

  19. Polymer-modified Fe0 nanoparticles target entrapped NAPL in two dimensional porous media: effect of particle concentration, NAPL saturation, and injection strategy.

    Science.gov (United States)

    Phenrat, Tanapon; Fagerlund, Fritjof; Illangasekare, Tissa; Lowry, Gregory V; Tilton, Robert D

    2011-07-15

    Polymer-modified nanoscale zerovalent iron (NZVI) particles are delivered into porous media for in situ remediation of nonaqueous phase liquid (NAPL) source zones. A systematic and quantitative evaluation of NAPL targeting by polymer-modified NZVI in two-dimensional (2-D) porous media under field-relevant conditions has not been reported. This work evaluated the importance of NZVI particle concentration, NAPL saturation, and injection strategy on the ability of polymer-modified NZVI (MRNIP2) to target the NAPL/water interface in situ in a 2-D porous media model. Dodecane was used as a NAPL model compound for this first demonstration of source zone targeting in 2-D. A driving force for NAPL targeting, the surface activity of MRNIP2 at the NAPL/water interface was verified ex situ by its ability to emulsify NAPL in water. MRNIP2 at low particle concentration (0.5 g/L) did not accumulate in or near entrapped NAPL, however, MRNIP2 at moderate and high particle concentrations (3 and 15 g/L) did accumulate preferentially at entrapped NAPL, i.e., it was capable of in situ targeting. The amount of MRNIP2 that targets a NAPL source depends on NAPL saturation (S(n)), presumably because the saturation controls the available NAPL/water interfacial area and the flow field through the NAPL source. At effective S(n) close or equal to 100%, MRNIP2 bypassed NAPL and accumulated only at the periphery of the entrapped NAPL region. At lower S(n), flow also carries MRNIP2 to NAPL/water interfaces internal to the entrapped NAPL region. However, the mass of accumulated MRNIP2 per unit available NAPL/water interfacial area is relatively constant (∼0.8 g/m(2) for MRNIP2 = 3 g/L) from S(n) = 13 to ∼100%, suggesting that NAPL targeting is mostly controlled by MRNIP2 sorption onto the NAPL/water interface.

  20. Solid polymer electrolyte composite membrane comprising a porous support and a solid polymer electrolyte including a dispersed reduced noble metal or noble metal oxide

    Science.gov (United States)

    Liu, Han; Mittelsteadt, Cortney K; Norman, Timothy J; Griffith, Arthur E; LaConti, Anthony B

    2015-02-24

    A solid polymer electrolyte composite membrane and method of manufacturing the same. According to one embodiment, the composite membrane comprises a thin, rigid, dimensionally-stable, non-electrically-conducting support, the support having a plurality of cylindrical, straight-through pores extending perpendicularly between opposing top and bottom surfaces of the support. The pores are unevenly distributed, with some or no pores located along the periphery and more pores located centrally. The pores are completely filled with a solid polymer electrolyte, the solid polymer electrolyte including a dispersed reduced noble metal or noble metal oxide. The solid polymer electrolyte may also be deposited over the top and/or bottom surfaces of the support.

  1. Porous bodies of hydroxyapatite produced by a combination of the gel-casting and polymer sponge methods.

    Science.gov (United States)

    González Ocampo, Jazmín I; Escobar Sierra, Diana M; Ossa Orozco, Claudia P

    2016-03-01

    A combination of gel-casting and polymeric foam infiltration methods is used in this study to prepare porous bodies of hydroxyapatite (HA), to provide a better control over the microstructures of samples. These scaffolds were prepared by impregnating a body of porous polyurethane foam with slurry containing HA powder, and using a percentage of solids between 40% and 50% w/v, and three different types of monomers to provide a better performance. X-Ray Diffraction (XRD), and Fourier Transformed Infrared (FTIR) and Scanning Electron Microscopy (SEM) were employed to evaluate both the powder hydroxyapatite and the scaffolds obtained. In addition, porosity and interconnectivity measurements were taken in accordance with the international norm. Bioactivity was checked using immersion tests in Simulated Body Fluids (SBF). After the sintering process of the porous bodies, the XRD results showed peaks characteristic of a pure and crystalline HA (JCPDS 9-432) as a single phase. SEM images indicate open and interconnected pores inside the material, with pore sizes between 50 and 600 μm. Also, SEM images demonstrate the relatively good bioactivity of the HA scaffolds after immersion in SBF. All results for the porous HA bodies suggest that these materials have great potential for use in tissue engineering.

  2. Bioresorbable Ca-phosphate-polymer/metal and Fe-Ag nanocomposites for macro-porous scaffolds with tunable degradation and drug release

    Science.gov (United States)

    Gotman, I.; Swain, S. K.; Sharipova, A.; Gutmanas, E. Y.

    2016-11-01

    Bioresorbable implants are increasingly gaining popularity as an attractive alternative to traditional permanent bone healing devices. The advantage of bioresorbable implantable devices is that they slowly degrade over time and disappear once their "mission" is accomplished. Thus, no foreign material is left behind that can cause adverse effects on the host, such as long term local or systemic immune response and stress-shielding related bone atrophy. Resorbable materials considered for surgical implant applications include degradable polymers, Ca phosphate ceramics (CaP) and corrodible metals. Degradable polymers, such as polycaprolactone and lactic acid are weak, lack osteoconductivity and degrade to acidic products that can cause late inflammation. Resorbable CaP ceramics (e.g., β-TCP) are attractive materials for bone regeneration bear close resemblance to the bone mineral, however they are intrinsically brittle and thus unsuitable for use in load-bearing sites. Moreover, introducing high porosity required to encourage better cellular ingrowth into bone regeneration scaffolds is detrimental to the mechanical strength of the material. In present work we review and discuss our results on development of strong bioresorbable Ca-phosphate-polymer/metal nanonocomposites and highly porous scaffolds from them. By introduction of nanoscale ductile polymer or metal phase into CaP ceramic an attempt was made to mimic structure of natural bone, where nanocrystallites of CaP ceramic are bonded by thin collagen layers. Recent results on development of high strength scaffolds from Fe-Ag nanocomposites are also reported. High energy milling of powders followed by cold sintering—high pressure consolidation at ambient temperature in combination with modified porogen leaching method was employed for processing. The developed nanocomposites and scaffolds exhibited high mechanical strength coupled with measurable ductility, gradual lost weight and strength during immersion in

  3. Incorporation of ionic liquid into porous polymer monoliths to enhance the separation of small molecules in reversed-phase high-performance liquid chromatography.

    Science.gov (United States)

    Wang, Jiafei; Bai, Ligai; Wei, Zhen; Qin, Junxiao; Ma, Yamin; Liu, Haiyan

    2015-06-01

    An ionic liquid was incorporated into the porous polymer monoliths to afford stationary phases with enhanced chromatographic performance for small molecules in reversed-phase high-performance liquid chromatography. The effect of the ionic liquid in the polymerization mixture on the performance of the monoliths was studied in detail. While monoliths without ionic liquid exhibited poor resolution and low efficiency, the addition of ionic liquid to the polymerization mixture provides highly increased resolution and high efficiency. The chromatographic performances of the monoliths were demonstrated by the separations of various small molecules including aromatic hydrocarbons, isomers, and homologues using a binary polar mobile phase. The present column efficiency reached 27 000 plates/m, which showed that the ionic liquid monoliths are alternative stationary phases in the separation of small molecules by high-performance liquid chromatography.

  4. Hollow porous ionic liquids composite polymers based solid phase extraction coupled online with high performance liquid chromatography for selective analysis of hydrophilic hydroxybenzoic acids from complex samples.

    Science.gov (United States)

    Dai, Xingping; Wang, Dongsheng; Li, Hui; Chen, Yanyi; Gong, Zhicheng; Xiang, Haiyan; Shi, Shuyun; Chen, Xiaoqing

    2017-02-10

    Polar and hydrophilic properties of hydroxybenzoic acids usually made them coelute with interferences in high performance liquid chromatography (HPLC) analysis. Then selective analysis of them was necessary. Herein, hollow porous ionic liquids composite polymers (PILs) based solid phase extraction (SPE) was firstly fabricated and coupled online with HPLC for selective analysis of hydroxybenzoic acids from complex matrices. Hollow porous PILs were firstly synthesized using Mobil Composition of Matter No. 48 (MCM-48) spheres as sacrificial support, 1-vinyl-3-methylimidazolium chloride (VMIM(+)Cl(-)) as monomer, and ethylene glycol dimethacrylate (EGDMA) as cross-linker. Various parameters affecting synthesis, adsorption and desorption behaviors were investigated and optimized. Steady-state adsorption studies showed the resulting hollow porous PILs exhibited high adsorption capacity, fast adsorption kinetics, and excellent specific adsorption. Subsequently, the application of online SPE system was studied by selective analysis of protocatechuic acid (PCA), 4-hydroxybenzoic acid (4-HBA), and vanillic acid (VA) from Pollen Typha angustifolia. The obtained limit of detection (LOD) varied from 0.002 to 0.01μg/mL, the linear range (0.05-5.0μg/mL) was wide with correlation coefficient (R) from 0.9982 to 0.9994, and the average recoveries at three spiking levels ranged from 82.7 to 102.4%, with column-to-column relative standard deviation (RSD) below 8.1%. The proposed online method showed good accuracy, precision, specificity and convenience, which opened up a universal and efficient route for selective analysis of hydroxybenzoic acids from complex samples.

  5. Porous rod-like MgO complex membrane with good anti-bacterial activity directed by conjugated linolenic acid polymer

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Hua-Jie, E-mail: wanghuajie972001@163.com; Chen, Meng [Henan Normal University, College of Chemistry and Chemical Engineering (China); Mi, Li-Wei, E-mail: mlwzzu@163.com [Zhongyuan University of Technology, Center for Advanced Materials Research (China); Shi, Li-Hua [Anyang 101 Education Center (China); Cao, Ying, E-mail: caoying1130@sina.com [Zhongyuan University of Technology, Center for Advanced Materials Research (China)

    2016-02-15

    The problem of infection in the tissue engineering substitutes is driving us to seek new coating materials. We previously found that conjugated linolenic acid (CLnA) has well biocompatibility and excellent membrane-forming property. The objective of this study is to endow the anti-bacterial activity to CLnA membra ne by linking with MgO. The results showed that the CLnA polymer membrane can be loaded with porous rod-like MgO and such complex membrane showed anti-bacterial sensitivity against gram-positive bacteria (Staphylococcus aureus) even at the low concentration (0.15 μg/mm{sup 2}). In the present study, the best zone of inhibition got to 18.2 ± 0.8 mm when the amount of MgO reach 2.42 ± 0.58 μg/mm{sup 2}. It was deduced that the porous rod-like structure of MgO was directed by CLnA in its polymerization process. Such CLnA/MgO complex membrane can be helpful in the tissue engineering, medicine, food engineering, food preservation, etc. on the basis of its good anti-bacterial activity.

  6. Finite Element Study on Performance of Piezoelectric Bimorph Cantilevers Using Porous/Ceramic 0-3 Polymer Composites

    Science.gov (United States)

    Kiran, Raj; Kumar, Anuruddh; Chauhan, Vishal S.; Kumar, Rajeev; Vaish, Rahul

    2017-09-01

    Finite element analysis of 0-3 composites made of piezoceramic particles and pores embedded in polyvinylidene difluoride (PVDF) has been carried out. The representative volume element (RVE) approach was used to calculate the effective elastic and piezoelectric properties of the periodic isotropic 0-3 piezoelectric composites. It was observed that the elastic and piezoelectric properties increased with the volume fraction of {K}_{0.475} {Na}_{0.475} {Li}_{0.05} ( {{Nb}_{0.92} {Ta}_{0.05} {Sb}_{0.03} } ){O}3 (KNLNTS) particles but decreased for the porous composites. These effective properties were further used to analyze the potential use of such bimorph cantilever beams in sensing and energy harvesting applications. Sensing voltage continuously increased for KNLNTS filled composites while for porous materials it increased up to 15% volume fraction porosity and then decreased. The same trend was also observed for the power produced by the harvester. However, the sensing voltage and power produced by harvesters made of porous composites were lower than for harvesters made of pure PVDF.

  7. Use of peak sharpening effects to improve the separation of chiral compounds with molecularly imprinted porous polymer layer open-tubular capillaries.

    Science.gov (United States)

    Kulsing, Chadin; Yang, Yuanzhong; Chowdhury, Jamil M; Boysen, Reinhard I; Hearn, Milton T W

    2017-02-17

    This investigation demonstrates the application of a new peak sharpening technique to improve the separation of difficult-to-resolve racemic mixtures in capillary electro-chromatography. Molecularly imprinted porous layer open tubular (MIP-PLOT) capillaries, prepared by a layer-on-layer polymerization approach with Z-l-Asp-OH as the template, were selected to validate the approach. SEM revealed that the polymer film thickness can be varied by changes in both the polymer composition and the layer-on-layer regime. Capillaries made with methacrylic acid as the functional monomer could not separate the Z-Asp-OH racemate, due to weak interactions between the MIP-PLOT material and the target analytes. In contrast, MIP-PLOT capillaries prepared with 4-vinylpyridine as the functional monomer resulted in increased ionic interactions with the target analytes. Separation of the enantiomers could be enhanced when a peak zone sharpening effect was exploited through the use of specific BGE compositions and by taking advantage of eigenpeak phenomena. In this manner, the position of a sharpening zone and the peak shape of the sample analytes could be fine-tuned, so that when the sharpening zone and the target analyte co-migrated the separation of the Z-l-Asp-OH enantiomer from its d-enantiomer in a racemic mixture could be achieved under overloading conditions.

  8. Selective metallization of polymers using laser induced surface activation (LISA)—characterization and optimization of porous surface topography

    DEFF Research Database (Denmark)

    Zhang, Yang; Hansen, Hans Nørgaard; De Grave, Arnaud

    2011-01-01

    Laser induced selective activation (LISA) is a molded interconnected devices technique for selective metallization of polymers. On the working piece, only the laser-machined area can be metalized in the subsequent plating. The principle of the technology is introduced. Surface analysis was perfor...

  9. Properties of the surface of a porous polymer modified with 5-fluorouracil, according to data of gas chromatography

    Science.gov (United States)

    Gus'kov, V. Yu.; Gainullina, Yu. Yu.; Ivanov, S. P.; Kudasheva, F. Kh.

    2014-06-01

    The effect or modification with 5-fluorouracil on the sorption activity of porous polymeric adsorbent is studied. It is demonstrated that the supramolecular structure formed on the surface is able to addition-ally contribute to the values of the specific retention volumes. It is found that the structure of 5-fluorouracil is capable of size effects corresponding to a molecular window of approximately 7-8 Å. It is concluded that surface polarity diminishes after modification, due to the shielding effect of four fluorine atoms present in the cavity.

  10. Imine-Linked Polymer Based Nitrogen-Doped Porous Activated Carbon for Efficient and Selective CO2 Capture

    Science.gov (United States)

    Alabadi, Akram; Abbood, Hayder A.; Li, Qingyin; Jing, Ni; Tan, Bien

    2016-12-01

    The preparation of nitrogen-doped activated carbon (NACs) has received significant attention because of their applications in CO2 capture and sequestration (CCS) owing to abundant nitrogen atoms on their surface and controllable pore structures by carefully controlled carbonization. We report high-surface-area porous N-doped activated carbons (NAC) by using soft-template-assisted self-assembly followed by thermal decomposition and KOH activation. The activation process was carried out under different temperature conditions (600–800 °C) using polyimine as precursor. The NAC-800 was found to have a high specific surface area (1900 m2 g‑1), a desirable micropore size below 1 nm and, more importantly, a large micropore volume (0.98 cm3 g‑1). NAC-800 also exhibits a significant capacity of CO2 capture i.e., over 6. 25 and 4.87 mmol g‑1 at 273 K and 298 K respectively at 1.13 bar, which is one of among the highest values reported for porous carbons so far. Moreover, NAC also shows an excellent separation selectivity for CO2 over N2.

  11. Theoretical examination of effective oxygen diffusion coefficient and electrical conductivity of polymer electrolyte fuel cell porous components

    Science.gov (United States)

    Inoue, Gen; Yokoyama, Kouji; Ooyama, Junpei; Terao, Takeshi; Tokunaga, Tomomi; Kubo, Norio; Kawase, Motoaki

    2016-09-01

    The reduction of oxygen transfer resistance through porous components consisting of a gas diffusion layer (GDL), microporous layer (MPL), and catalyst layer (CL) is very important to reduce the cost and improve the performance of a PEFC system. This study involves a systematic examination of the relationship between the oxygen transfer resistance of the actual porous components and their three-dimensional structure by direct measurement with FIB-SEM and X-ray CT. Numerical simulations were carried out to model the properties of oxygen transport. Moreover, based on the model structure and theoretical equations, an approach to the design of new structures is proposed. In the case of the GDL, the binder was found to obstruct gas diffusion with a negative effect on performance. The relative diffusion coefficient of the MPL is almost equal to that of the model structure of particle packing. However, that of CL is an order of magnitude less than those of the other two components. Furthermore, an equation expressing the relative diffusion coefficient of each component can be obtained with the function of porosity. The electrical conductivity of MPL, which is lower than that of the carbon black packing, is considered to depend on the contact resistance.

  12. Imine-Linked Polymer Based Nitrogen-Doped Porous Activated Carbon for Efficient and Selective CO2 Capture

    Science.gov (United States)

    Alabadi, Akram; Abbood, Hayder A.; Li, Qingyin; Jing, Ni; Tan, Bien

    2016-01-01

    The preparation of nitrogen-doped activated carbon (NACs) has received significant attention because of their applications in CO2 capture and sequestration (CCS) owing to abundant nitrogen atoms on their surface and controllable pore structures by carefully controlled carbonization. We report high-surface-area porous N-doped activated carbons (NAC) by using soft-template-assisted self-assembly followed by thermal decomposition and KOH activation. The activation process was carried out under different temperature conditions (600–800 °C) using polyimine as precursor. The NAC-800 was found to have a high specific surface area (1900 m2 g−1), a desirable micropore size below 1 nm and, more importantly, a large micropore volume (0.98 cm3 g−1). NAC-800 also exhibits a significant capacity of CO2 capture i.e., over 6. 25 and 4.87 mmol g−1 at 273 K and 298 K respectively at 1.13 bar, which is one of among the highest values reported for porous carbons so far. Moreover, NAC also shows an excellent separation selectivity for CO2 over N2. PMID:27958305

  13. Modified MODFLOW-based model for simulating the agglomeration and transport of polymer-modified Fe(0) nanoparticles in saturated porous media.

    Science.gov (United States)

    Babakhani, Peyman; Fagerlund, Fritjof; Shamsai, Abolfazl; Lowry, Gregory V; Phenrat, Tanapon

    2015-08-25

    The solute transport model MODFLOW has become a standard tool in risk assessment and remediation design. However, particle transport models that take into account both particle agglomeration and deposition phenomena are far less developed. The main objective of the present study was to evaluate the feasibility of adapting the standard code MODFLOW/MT3D to simulate the agglomeration and transport of three different types of polymer-modified nanoscale zerovalent iron (NZVI) in one-dimensional (1-D) and two-dimensional (2-D) saturated porous media. A first-order decay of the particle population was used to account for the agglomeration of particles. An iterative technique was used to optimize the model parameters. The model provided good matches to 1-D NZVI-breakthrough data sets, with R (2) values ranging from 0.96 to 0.99, and mass recovery differences between the experimental results and simulations ranged from 0.1 to 1.8 %. Similarly, simulations of NZVI transport in the heterogeneous 2-D model demonstrated that the model can be applied to more complicated heterogeneous domains. However, the fits were less good, with the R (2) values in the 2-D modeling cases ranging from 0.75 to 0.95, while the mass recovery differences ranged from 0.7 to 6.5 %. Nevertheless, the predicted NZVI concentration contours during transport were in good agreement with the 2-D experimental observations. The model provides insights into NZVI transport in porous media by mathematically decoupling agglomeration, attachment, and detachment, and it illustrates the importance of each phenomenon in various situations. Graphical Abstract ᅟ.

  14. From microporous regular frameworks to mesoporous materials with ultrahigh surface area: dynamic reorganization of porous polymer networks.

    Science.gov (United States)

    Kuhn, Pierre; Forget, Aurélien; Su, Dangsheng; Thomas, Arne; Antonietti, Markus

    2008-10-08

    High surface area organic materials featuring both micro- and mesopores were synthesized under ionothermal conditions via the formation of polyaryltriazine networks. While the polytrimerization of nitriles in zinc chloride at 400 degrees C produces microporous polymers, higher reaction temperatures induce the formation of additional spherical mesopores with a narrow dispersity. The nitrogen-rich carbonaceous polymer materials thus obtained present surface areas and porosities up to 3300 m(2) g(-1) and 2.4 cm(3) g(-1), respectively. The key point of this synthesis relies on the occurrence of several high temperature polymerization reactions, where irreversible carbonization reactions coupled with the reversible trimerization of nitriles allow the reorganization of the dynamic triazine network. The ZnCl2 molten salt fulfills the requirement of a high temperature solvent, but is also required as catalyst. Thus, this dynamic polymerization system provides not only highly micro- and mesoporous materials, but also allows controlling the pore structure in amorphous organic materials.

  15. Polymer@MOF@MOF: "grafting from" atom transfer radical polymerization for the synthesis of hybrid porous solids.

    Science.gov (United States)

    McDonald, Kyle A; Feldblyum, Jeremy I; Koh, Kyoungmoo; Wong-Foy, Antek G; Matzger, Adam J

    2015-08-04

    The application of a core-shell architecture allows the formation of a polymer-coated metal-organic framework (MOF) maintaining high surface area (2289-2857 m(2) g(-1)). The growth of a MOF shell from a MOF core was used to spatially localize initiators by post-synthetic modification. The confinement of initiators ensures that polymerization is restricted to the outer shell of the MOF.

  16. Reversible Guest Binding in a Non-Porous FeII Coordination Polymer Host Toggles Spin Crossover

    DEFF Research Database (Denmark)

    Lennartson, Anders; Southon, Peter; Sciortino, Natasha F.

    2015-01-01

    )4 CN)2 ](SbF6 )4 ( 2 ) are low spin at room temperature, as are those in the polymeric adiponitrile-linked acetone solvate polymer {[Fe(bpte)(μ2-NC(CH2)4CN)]-(BPh4)2⋅Me2CO} ( 3⋅ Me2 CO). On heating 3⋅ Me2CO to 80 °C, the acetone is abruptly removed with an accompanying purple to dull lavender colour...

  17. Nanoparticle-Directed Metal-Organic Framework/Porous Organic Polymer Monolithic Supports for Flow-Based Applications.

    Science.gov (United States)

    Darder, María Del Mar; Salehinia, Shima; Parra, José B; Herrero-Martinez, José M; Svec, Frantisek; Cerdà, Víctor; Turnes Palomino, Gemma; Maya, Fernando

    2017-01-18

    A two-step nanoparticle-directed route for the preparation of macroporous polymer monoliths for which the pore surface is covered with a metal-organic framework (MOF) coating has been developed to facilitate the use of MOFs in flow-based applications. The flow-through monolithic matrix was prepared in a column format from a polymerization mixture containing ZnO-nanoparticles. These nanoparticles embedded in the precursor monolith were converted to MOF coatings via the dissolution-precipitation equilibrium after filling the pores of the monolith with a solution of the organic linker. Pore surface coverage with the microporous zeolitic imidazolate framework ZIF-8 resulted in an increase in surface area from 72 to 273 m(2) g(-1). Monolithic polymer containing ZIF-8 coating was implemented as a microreactor catalyzing the Knoevenagel condensation reaction and also in extraction column format enabling the preconcentration of trace levels of toxic chlorophenols in environmental waters. Our approach can be readily adapted to other polymers and MOFs thus enabling development of systems for flow-based MOF applications.

  18. Two-step adsorption on jungle-gym-type porous coordination polymers: dependence on hydrogen-bonding capability of adsorbates, ligand-substituent effect, and temperature.

    Science.gov (United States)

    Uemura, Kazuhiro; Yamasaki, Yukari; Onishi, Fumiaki; Kita, Hidetoshi; Ebihara, Masahiro

    2010-11-01

    A preliminary study of isopropanol (IPA) adsorption/desorption isotherms on a jungle-gym-type porous coordination polymer, [Zn(2)(bdc)(2)(dabco)](n) (1, H(2)bdc = 1,4-benzenedicarboxylic acid, dabco =1,4-diazabicyclo[2.2.2]octane), showed unambiguous two-step profiles via a highly shrunk intermediate framework. The results of adsorption measurements on 1, using probing gas molecules of alcohol (MeOH and EtOH) for the size effect and Me(2)CO for the influence of hydrogen bonding, show that alcohol adsorption isotherms are gradual two-step profiles, whereas the Me(2)CO isotherm is a typical type-I isotherm, indicating that a two-step adsorption/desorption is involved with hydrogen bonds. To further clarify these characteristic adsorption/desorption behaviors, selecting nitroterephthalate (bdc-NO(2)), bromoterephthalate (bdc-Br), and 2,5-dichloroterephthalate (bdc-Cl(2)) as substituted dicarboxylate ligands, isomorphous jungle-gym-type porous coordination polymers, {[Zn(2)(bdc-NO(2))(2)(dabco)]·solvents}(n) (2 ⊃ solvents), {[Zn(2)(bdc-Br)(2)(dabco)]·solvents}(n) (3 ⊃ solvents), and {[Zn(2)(bdc-Cl(2))(2)(dabco)]·solvents}(n) (4 ⊃ solvents), were synthesized and characterized by single-crystal X-ray analyses. Thermal gravimetry, X-ray powder diffraction, and N(2) adsorption at 77 K measurements reveal that [Zn(2)(bdc-NO(2))(2)(dabco)](n) (2), [Zn(2)(bdc-Br)(2)(dabco)](n) (3), and [Zn(2)(bdc-Cl(2))(2)(dabco)](n) (4) maintain their frameworks without guest molecules with Brunauer-Emmett-Teller (BET) surface areas of 1568 (2), 1292 (3), and 1216 (4) m(2) g(-1). As found in results of MeOH, EtOH, IPA, and Me(2)CO adsorption/desorption on 2-4, only MeOH adsorption on 2 shows an obvious two-step profile. Considering the substituent effects and adsorbate sizes, the hydrogen bonds, which are triggers for two-step adsorption, are formed between adsorbates and carboxylate groups at the corners in the pores, inducing wide pores to become narrow pores. Interestingly, such

  19. Extra dissipation and flow uniformization due to elastic instabilities of shear-thinning polymer solutions in model porous media

    Science.gov (United States)

    Machado, Anaïs; Bodiguel, Hugues; Beaumont, Julien; Clisson, Gérald; Colin, Annie

    2016-01-01

    We study flows of hydrolized polyacrylamide solutions in two dimensional porous media made using microfluidics, for which elastic effects are dominant. We focus on semi-dilute solutions (0.1%–0.4%) which exhibit a strong shear thinning behavior. We systematically measure the pressure drop and find that the effective permeability is dramatically higher than predicted when the Weissenberg number is greater than about 10. Observations of the streamlines of the flow reveal that this effect coincides with the onset of elastic instabilities. Moreover, and importantly for applications, we show using local measurements that the mean flow is modified: it appears to be more uniform at high Weissenberg number than for Newtonian fluids. These observations are compared and discussed using pore network simulations, which account for the effect of disorder and shear thinning on the flow properties. PMID:27478522

  20. Porous polymer monoliths functionalized through copolymerization of a C60 fullerene-containing methacrylate monomer for highly efficient separations of small molecules

    KAUST Repository

    Chambers, Stuart D.

    2011-12-15

    Monolithic poly(glycidyl methacrylate-co-ethylene dimethacrylate) and poly(butyl methacrylate-co-ethylene dimethacrylate) capillary columns, which incorporate the new monomer [6,6]-phenyl-C 61-butyric acid 2-hydroxyethyl methacrylate ester, have been prepared and their chromatographic performance have been tested for the separation of small molecules in the reversed phase. While addition of the C60-fullerene monomer to the glycidyl methacrylate-based monolith enhanced column efficiency 18-fold, to 85 000 plates/m at a linear velocity of 0.46 mm/s and a retention factor of 2.6, when compared to the parent monolith, the use of butyl methacrylate together with the carbon nanostructured monomer afforded monolithic columns with an efficiency for benzene exceeding 110 000 plates/m at a linear velocity of 0.32 mm/s and a retention factor of 4.2. This high efficiency is unprecedented for separations using porous polymer monoliths operating in an isocratic mode. Optimization of the chromatographic parameters affords near baseline separation of 6 alkylbenzenes in 3 min with an efficiency of 64 000 plates/m. The presence of 1 wt % or more of water in the polymerization mixture has a large effect on both the formation and reproducibility of the monoliths. Other factors such as nitrogen exposure, polymerization conditions, capillary filling method, and sonication parameters were all found to be important in producing highly efficient and reproducible monoliths. © 2011 American Chemical Society.

  1. Hyper-crosslinked β-cyclodextrin porous polymer: an adsorption-facilitated molecular catalyst support for transformation of water-soluble aromatic molecules.

    Science.gov (United States)

    Li, Haiying; Meng, Bo; Chai, Song-Hai; Liu, Honglai; Dai, Sheng

    2016-02-01

    A hyper-crosslinked β-cyclodextrin porous polymer (BnCD-HCPP) was designed and synthesized facilely by β-cyclodextrin benzylation and subsequent crosslinking via a Friedel-Crafts alkylation route. The BnCD-HCPP shows an extremely high BET surface area, large pore volume, and high thermal stability, making it a highly efficient adsorbent for removal of aromatic pollutants from water. The adsorption efficiency in terms of distribution coefficient, defined as the ratio of adsorption capacity to equilibrium adsorbate concentration, ranged from 10(3) to 10(6) mL g(-1) within a concentration of 0-100 ppm, one order of magnitude higher than that of other β-cyclodextrin-based adsorbents reported previously. The molar percentage of adsorbate to β-cyclodextrin exceeded 300%, suggesting that the adsorption occurred not only in the cyclodextrin cavities via a 1 : 1 complexation, but also in the nanopores of the BnCD-HCPP created during the hyper-crosslinking. The BnCD-HCPP can be further functionalized by incorporation of gold nanoparticles for catalytic transformation of adsorbed phenolic compounds such as 4-nitrophenol to 4-aminophenol.

  2. An effective and in-situ method based tresyl-functionalized porous polymer material for enrichment and digestion of membrane proteins and its application in extraction tips.

    Science.gov (United States)

    Wang, Jiaxi; Gao, Mingxia; Yan, Guoquan; Zhang, Xiangmin

    2015-06-23

    Membrane proteins are one of promising targets for drug discovery because of the unique properties in physiological processes. Due to their low abundance and extremely hydrophobic nature, the analysis of membrane proteins is still a great challenge. In this work, an effective and in-situ method were developed to enrich and digest membrane proteins by adopting tresyl-functionalized porous polymer material. With tresyl groups, the material can effectively immobilize membrane proteins via covalent bonding on the surface. The material became a facile carrier to enrich membrane proteins from the rat liver in detergents and organic solvents owing to its outstanding binding capacity and excellent biocompatibility. Moreover, it was further applied in extraction tips to capture and in-situ digest the pretreatment membrane proteins in two different solutions. A total of 600 membrane proteins (51% of total protein groups) and 359 transmembrane proteins were identified by nano-LC-ESI-MS/MS in 4% sodium dodecyl sulfate (SDS), and similar results were achieved in the 60% methanol solution. All these results demonstrated that the new approach is of great promise for large-scale characterization of membrane proteins.

  3. Effect of porous structure of catalyst layer on effective oxygen diffusion coefficient in polymer electrolyte fuel cell

    Science.gov (United States)

    Inoue, Gen; Kawase, Motoaki

    2016-09-01

    It is important to reduce the oxygen diffusion resistance through PEFC porous electrode, because it is the key to reduce the PEFC cost. However, the gas diffusion coefficient of CL is lower than MPL in spite of framework consisted of same carbon blacks. In this study, in order to understand the reasons of the lower gas diffusion performance of CL, the relationship between a carbon black agglomerate structure and ionomer adhesion condition is evaluated by a numerical analysis with an actual reconstructed structure and a simulated structure. As a result, the gas diffusion property of CL strongly depends on the ionomer adhesion shape. In the case of adhesion shape with the same curvature of ionomer interface, each pore can not be connected enough. So the pore tortuosity increases. Moreover, in the case of existence of inefficient large pores formed by carbon black agglomerate and ununiformly coated ionomer, the gas diffusion performance decrease rapidly. As the measurement values in actual CL are almost equal to that with model structure with inefficient large pores. These characteristics can be confirmed by actual cross-section image obtained by FIB-SEM.

  4. Divergent kinetic and thermodynamic hydration of a porous Cu(II) coordination polymer with exclusive CO₂ sorption selectivity.

    Science.gov (United States)

    Du, Miao; Li, Cheng-Peng; Chen, Min; Ge, Zhi-Wei; Wang, Xi; Wang, Lei; Liu, Chun-Sen

    2014-08-06

    Selective adsorption and separation of CO2 are of great importance for different target applications. Metal-organic frameworks (MOFs) represent a promising class of porous materials for this purpose. Here we present a unique MOF material, [Cu(tba)2]n (tba = 4-(1H-1,2,4-triazol-1-yl)benzoate), which shows high CO2 adsorption selectivity over CH4/H2/O2/Ar/N2 gases (with IAST selectivity of 41-68 at 273 K and 33-51 at 293 K). By using a critical point dryer, the CO2 molecules can be well sealed in the 1D channels of [Cu(tba)2]n to allow a single-crystal X-ray analysis, which reveals the presence of not only C(δ+)-H···O(δ-) bonds between the host framework and CO2 but also quadrupole-quadrupole (CO2(δ-)···(δ+)CO2) interactions between the CO2 molecules. Furthermore, [Cu(tba)2]n will suffer divergent kinetic and thermodynamic hydration processes to form its isostructural hydrate {[Cu(tba)2](H2O)}n and a mononuclear complex [Cu(tba)2(H2O)4] via single-crystal to single-crystal transformations.

  5. Pickering乳液模板法制备多孔分子印迹聚合物的进展%Development of Porous Imprinted Polymers Synthesized via Pickering Emulsion Template

    Institute of Scientific and Technical Information of China (English)

    潘建明; 殷毅杰

    2016-01-01

    This work reviews the studies about porous imprinted polymers via Pickering emulsion template .The hollow imprinted polymers , porous imprinted polymers and imprinted polymer foams can be prepared by Pickering single emulsion ,Pickering double emulsion and Pickering high internal phase emulsion ,respectively , and their interface behaviors and structure-activity relationship were described .Meanwhile, the merits, disadvantages and application fields of three emulsion template were commented .Finally ,the expectation of this research containing the selection of micro/nano particles ,formation ways of stable emulsion was illustrated .%对近年来Pickering乳液模板法制备多孔分子印迹聚合物的工作进行了总结,阐述了Pickering单乳液、Pickering双乳液以及Pickering高内相乳液法分别制备中空、多孔微球以及泡沫的结构分子印迹聚合物的过程、界面行为调控和对应构效关系;指出了3类方法的优势、适用范围与存在的不足之处,并对微纳米稳定粒子选择、乳液形成方式、应用领域拓展等方面的研究设想进行了展望。

  6. Hydrophobic, Porous Battery Boxes

    Science.gov (United States)

    Bragg, Bobby J.; Casey, John E., Jr.

    1995-01-01

    Boxes made of porous, hydrophobic polymers developed to contain aqueous potassium hydroxide electrolyte solutions of zinc/air batteries while allowing air to diffuse in as needed for operation. Used on other types of batteries for in-cabin use in which electrolytes aqueous and from which gases generated during operation must be vented without allowing electrolytes to leak out.

  7. Porous and Magnetic Molecularly Imprinted Polymers via Pickering High Internal Phase Emulsions Polymerization for Selective Adsorption of λ-Cyhalothrin

    Science.gov (United States)

    Wu, Yunlong; Ma, Yue; Pan, Jianming; Gu, Runxing; Luo, Jialu

    2017-01-01

    A novel macroporous magnetic molecularly imprinted polymer (MMIPs) of was prepared by W/O Pickering (high internal phase emulsions) HIPEs polymerization, and then it was adopted as adsorbent for selective adsorption of λ-cyhalothrin (LC). In static conditions, adsorption capacity of LC increased rapidly in the first 60 min and reached to equilibrium in ~2.0 h. Excellent conformity of the second-order model confirmed the chemical nature of the interaction between the LC and imprinted sites. The fitting adsorption isotherm was a Langmuir type, and the maximum monolayer adsorption capacity at 298 K was 404.4 μmol g−1. Thermodynamic parameters suggested the specific adsorption at 298 K was an exothermic, spontaneous, and entropy decreased process. Competitive recognition studies of the MMIPs were performed with diethyl phthalate (DEP) and the structurally similar compound fenvalerate (FL), and the MMIPs, which displayed high selectivity for LC.

  8. Effect of Solvent Molecule in Pore for Flexible Porous Coordination Polymer upon Gas Adsorption and Iodine Encapsulation.

    Science.gov (United States)

    Arıcı, Mürsel; Yeşilel, Okan Zafer; Taş, Murat; Demiral, Hakan

    2015-12-07

    Four new Zn(II)-coordination polymers, namely, [Zn2(μ6-ao2btc)(μ-obix)2]n (1), [Zn2(μ4-ao2btc)(μ-obix)2]n (2), [Zn2(μ4-ao2btc)(μ-mbix)2]n (3), and {[Zn2(μ4-ao2btc)(μ-pbix)2] · 2DMF · 8H2O}n (4), where ao2btc = dioxygenated form of 3,3',5,5'-azobenzenetetracarboxylate and obix, mbix, and pbix = 1,2-, 1,3-, and 1,4-bis(imidazol-1-ylmethyl)benzene, have been synthesized with azobenzenetetracarboxylic acid and isomeric bis(imidazole) ligands and characterized by elemental analyses, IR spectra, single-crystal X-ray diffraction, powder X-ray diffraction, and thermal analyses. X-ray results showed that 1, 2, and 4 had two-dimensional structures with 3,4L13 topology, while 3 was a three-dimensional coordination polymer with bbf topology. For 4, two types of activation strategies, solvent exchange + heating (which produced 4a) and direct heating (which produced 4b), were used to investigate the effect of a guest molecule in a flexible framework. Gas adsorption and iodine encapsulation properties of activated complexes were studied. The CO2 uptake capacities for 4a and 4b were 3.62% and 9.50%, respectively, and Langmuir surface areas calculated from CO2 isotherms were 167.4 and 350.7 m(2)/g, respectively. Moreover, 4b exhibited 19.65% and 15.27% iodine uptake in vapor phase and cyclohexane solution, respectively, which corresponded to 1.47 and 0.97 molecules of iodine/formula unit, respectively. Moreover, photoluminescence properties of the complexes were studied.

  9. Embedding nano-Li{sub 4}Ti{sub 5}O{sub 12} in hierarchical porous carbon matrixes derived from water soluble polymers for ultra-fast lithium ion batteries anodic materials

    Energy Technology Data Exchange (ETDEWEB)

    Lan, Chun-Kai; Bao, Qi; Huang, Yao-Hui; Duh, Jenq-Gong, E-mail: jgd@mx.nthu.edu.tw

    2016-07-15

    Li{sub 4}Ti{sub 5}O{sub 12}/hierarchical porous carbon matrixes composites are successfully prepared by a facile and fast polymers assisted sol–gel method, aiming to promote both electronic and ionic conductivity. As indicated by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy analysis, three less expensive cost and available water soluble polymers (e.g. PAA, CMC, and SA) can homogeneously react with Li–Ti–O precursor to incorporate into interior of nano-scale lithium titanate and provide a continues conductive network after pyrolysis. In addition, the results of scanning electron microscopy and transmission electron microscopy also prove that the Li{sub 4}Ti{sub 5}O{sub 12} nanoparticles are firmly embedded in porous carbon matrix with no obvious agglomeration. EIS measurement and cyclic voltammetry further reveal that the facilitated electrode kinetics and better ionic transport of Li{sub 4}Ti{sub 5}O{sub 12}/hierarchical porous carbon matrixes composites than that of Li{sub 4}Ti{sub 5}O{sub 12}. The c-CMC-LTO exhibits a superior capacity of 92 mAh g{sup −1} and retains its initial value with no obviously capacity decay over 200 cycles under an ultra-high C rate (50 C). - Graphical abstract: Schematic illustrations of the formation process of embedding LTO into Carbon matrixes derived from water soluable polymers (upper) and the electrochemical reaction paths in LTO/Carbon composites during charging/discharging processes (lower). - Highlights: • Hierarchical porous carbon matrixes were used to improve the Li{sub 4}Ti{sub 5}O{sub 12} anodes. • Carbon matrixes could suppress the agglomeration of Li{sub 4}Ti{sub 5}O{sub 12} nanoparticles. • meso-nanoporous carbon structure was beneficial for filtration of electrolyte. • The c-CMC-LTO exhibited superior high rate capability and cycling durability.

  10. Composite solid polymer electrolyte membranes

    Energy Technology Data Exchange (ETDEWEB)

    Formato, Richard M. (Shrewsbury, MA); Kovar, Robert F. (Wrentham, MA); Osenar, Paul (Watertown, MA); Landrau, Nelson (Marlborough, MA); Rubin, Leslie S. (Newton, MA)

    2001-06-19

    The present invention relates to composite solid polymer electrolyte membranes (SPEMs) which include a porous polymer substrate interpenetrated with an ion-conducting material. SPEMs of the present invention are useful in electrochemical applications, including fuel cells and electrodialysis.

  11. Peclet number analysis of cross-flow in porous gas diffusion layer of polymer electrolyte membrane fuel cell (PEMFC).

    Science.gov (United States)

    Suresh, P V; Jayanti, Sreenivas

    2016-10-01

    Adoption of hydrogen economy by means of using hydrogen fuel cells is one possible solution for energy crisis and climate change issues. Polymer electrolyte membrane (PEM) fuel cell, which is an important type of fuel cells, suffers from the problem of water management. Cross-flow is induced in some flow field designs to enhance the water removal. The presence of cross-flow in the serpentine and interdigitated flow fields makes them more effective in proper distribution of the reactants on the reaction layer and evacuation of water from the reaction layer than diffusion-based conventional parallel flow fields. However, too much of cross-flow leads to flow maldistribution in the channels, higher pressure drop, and membrane dehydration. In this study, an attempt has been made to quantify the amount of cross-flow required for effective distribution of reactants and removal of water in the gas diffusion layer. Unit cells containing two adjacent channels with gas diffusion layer (GDL) and catalyst layer at the bottom have been considered for the parallel, interdigitated, and serpentine flow patterns. Computational fluid dynamics-based simulations are carried out to study the reactant transport in under-the-rib area with cross-flow in the GDL. A new criterion based on the Peclet number is presented as a quantitative measure of cross-flow in the GDL. The study shows that a cross-flow Peclet number of the order of 2 is required for effective removal of water from the GDL. Estimates show that this much of cross-flow is not usually produced in the U-bends of Serpentine flow fields, making these areas prone to flooding.

  12. Bimodal porous TiO2 structures templated by graft copolymer/homopolymer blend for dye-sensitized solar cells with polymer electrolyte

    Science.gov (United States)

    Kim, Jin Kyu; Lee, Chang Soo; Lee, Sang-Yup; Cho, Hyung Hee; Kim, Jong Hak

    2016-12-01

    Bimodal porous TiO2 (BP-TiO2) with large surface area, high porosity, good interconnectivity, and excellent light-scattering ability are synthesized via a facile one-step method using a self-assembled blend template consisting of an amphiphilic poly(vinyl chloride)-g-poly(oxyethylene methacrylate) (PVC-g-POEM) graft copolymer and a hydrophobic poly(vinyl chloride) (PVC) homopolymer. The hydrophilically surface-modified TiO2 nanoparticles selectively interact with the hydrophilic POEM chains, while the addition of the PVC homopolymer increases the hydrophobic domain size, resulting in the formation of dual pores (i.e., macropores and mesopores). The sizes and numbers of macropores can easily be controlled by changing the molecular weight and amount of the PVC homopolymer. The polymer electrolyte dye-sensitized solar cells (DSSCs) fabricated with BP-TiO2 photoanodes exhibited energy conversion efficiencies of up to 7.6% at 100 mW cm-2, which is much higher than those of mesoporous TiO2 (5.8%) with PVC-g-POEM only and conventional nanocrystalline TiO2 (4.9%) with commercial Dyesol paste. The enhanced energy conversion efficiencies mostly resulted from the light-scattering effects of the macropores, which increased the light-harvesting efficiencies. The improved light-harvesting and photovoltaic performances of the DSSCs were characterized by UV-vis spectroscopy, incident photon-to-current conversion efficiency analysis, electrochemical impedance spectroscopy, intensity-modulated photocurrent spectroscopy, and intensity-modulated photovoltage spectroscopy.

  13. Shape-anchored porous polymer monoliths for integrated online solid-phase extraction-microchip electrophoresis-electrospray ionization mass spectrometry.

    Science.gov (United States)

    Nordman, Nina; Barrios-Lopez, Brianda; Laurén, Susanna; Suvanto, Pia; Kotiaho, Tapio; Franssila, Sami; Kostiainen, Risto; Sikanen, Tiina

    2015-02-01

    We report a simple protocol for fabrication of shape-anchored porous polymer monoliths (PPMs) for on-chip SPE prior to online microchip electrophoresis (ME) separation and on-chip (ESI/MS). The chip design comprises a standard ME separation channel with simple cross injector and a fully integrated ESI emitter featuring coaxial sheath liquid channel. The monolith zone was prepared in situ at the injection cross by laser-initiated photopolymerization through the microchip cover layer. The use of high-power laser allowed not only maskless patterning of a precisely defined monolith zone, but also faster exposure time (here, 7 min) compared with flood exposure UV lamps. The size of the monolith pattern was defined by the diameter of the laser output (∅500 μm) and the porosity was geared toward high through-flow to allow electrokinetic actuation and thus avoid coupling to external pumps. Placing the monolith at the injection cross enabled firm anchoring based on its cross-shape so that no surface premodification with anchoring linkers was needed. In addition, sample loading and subsequent injection (elution) to the separation channel could be performed similar to standard ME setup. As a result, 15- to 23-fold enrichment factors were obtained already at loading (preconcentration) times as short as 25 s without sacrificing the throughput of ME analysis. The performance of the SPE-ME-ESI/MS chip was repeatable within 3.1% and 11.5% RSD (n = 3) in terms of migration time and peak height, respectively, and linear correlation was observed between the loading time and peak area.

  14. Fabricating porous materials using interpenetrating inorganic-organic composite gels

    Science.gov (United States)

    Seo, Dong-Kyun; Volosin, Alex

    2016-06-14

    Porous materials are fabricated using interpenetrating inorganic-organic composite gels. A mixture or precursor solution including an inorganic gel precursor, an organic polymer gel precursor, and a solvent is treated to form an inorganic wet gel including the organic polymer gel precursor and the solvent. The inorganic wet gel is then treated to form a composite wet gel including an organic polymer network in the body of the inorganic wet gel, producing an interpenetrating inorganic-organic composite gel. The composite wet gel is dried to form a composite material including the organic polymer network and an inorganic network component. The composite material can be treated further to form a porous composite material, a porous polymer or polymer composite, a porous metal oxide, and other porous materials.

  15. Gradient-porous structure of silicon

    Energy Technology Data Exchange (ETDEWEB)

    Starkov, V.; Gavrilin, E. [Institute of Microelectronics Technology and High Purite Materials RAS, Institutskya str. 6, Chernogolovka 142432 (Russian Federation)

    2007-07-01

    Silicon membranes with through pores have been manufactured based on silicon plates with a gradient-porous structure (GPSi), in which the pore cross section and structure varies with depth. The obtained structure can serve a basis for the development of electrodes for solid polymer fuel cells. The developed technology allows to change porosity and porous morphology on all thickness of a porous membrane. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  16. Sulfur cathode hosted in porous organic polymeric matrices

    Science.gov (United States)

    Zhang, Zhengcheng; Weng, Wei; Yuan, Shengwen; Amine, Khalil

    2016-02-09

    A composite material includes a porous organic polymer and an electrochemically active material, wherein the porous organic polymer contains a plurality of pores having a diameter of from about 0.1 nm to about 100 nm, and the electrochemically active material is disposed within the pores.

  17. Porous bioactive materials

    Science.gov (United States)

    Zhang, Kai

    Bioactive materials chemically bond to tissues through the development of biologically active apatite. Porous structures in biomaterials are designed to enhance bioactivity, grow artificial tissues and achieve better integration with host tissues in the body. The goal of this research is to design, fabricate and characterize novel porous bioactive materials. 3D ordered macroporous bioactive glasses (3DOM-BGs, pore size: 200--1000 nm) were prepared using a sol-gel process and colloidal crystal templates. 3DOM-BGs are more bioactive and degradable than mesoporous (pore size simulated body fluid (SBF). Apatite formation and 3DOM-BG degradation rates increased with the decrease of soaking ratio. Apatite induction time in SBF increased with 3DOM-BG calcination temperature (600--800°C). Apatite formation and 3DOMBG degradation were slightly enhanced for a phosphate containing composition. Large 3DOM-BG particles formed less apatite and degraded less completely as compared with small particles. An increase in macropore size slowed down 3DOM-BG degradation and apatite formation processes. After heating the converted apatite at a temperature higher than 700°C, highly crystalline hydroxyapatite and a minor tri-calcium phosphate phase formed. 3DOM-BGs have potential applications as bone/periodontal fillers, and drugs and biological factors delivery agents. Anchoring artificial soft tissues (e.g., cartilage) to native bone presents a challenge. Porous polymer/bioactive glass composites are candidate materials for engineering artificial soft tissue/bone interfaces. Porous composites consisting of polymer matrices (e.g., polysulfone, polylactide, and polyurethane) and bioactive glass particles were prepared by polymer phase separation techniques adapted to include ceramic particles. Composites (thickness: 200--500 mum) have asymmetric structures with dense top layers and porous structures beneath. Porous structures consist of large pores (>100 mum) in a network of smaller (<10

  18. Progress of CO2 capture and separation by porous organic polymers%有机多孔聚合物CO2捕集及分离性能的研究进展

    Institute of Scientific and Technical Information of China (English)

    朱祥; 吕文杰; 胡军; 汪华林; 刘洪来

    2014-01-01

    有机多孔聚合物(porous organic polymers,POPs)是一类由有机构建单元连接而形成的新型多孔材料。由于其优异的物理化学稳定性以及CO2吸附能力,近年来有关POPs在CO2捕集和分离的研究成为一大研究热点。大量具有优异孔性质(比表面积和孔容)的POPs通过不同有机合成反应被成功地开发出来应用于CO2吸附分离过程。本文介绍了POPs材料的CO2捕集与分离性能的研究现状,总结了提高POPs材料CO2分离性能的合成策略,重点分析了可以通过功能化增强吸附剂与二氧化碳分子之间的相互作用,来提高材料的CO2分离能力的方法。%Porous organic polymers (POPs), a new type of porous materials constructed by organic building blocks, have attracted attention and shown significant potential for CO2 capture and separation due to their high physicochemical stability and excellent adsorption capacity. Numerous POPs with good porosity (both surface area and pore volume) are preparedvia different organic reactions. The progress of capture and separation of CO2 by POPs is reviewed. Several potential strategies like increasing isosteric heats between sorbent and CO2 molecules by chemical functionalization for enhancing CO2 separation performance are summarized.

  19. Preparation and characterisation of porous poly(2,5benzimidazole) (ABPBI) membranes using surfactants as templates for polymer electrolyte membrane fuel cells

    CSIR Research Space (South Africa)

    Zheng, H

    2010-04-01

    Full Text Available properties on mechanical strengths, thermal stability and electrochemical performance when compared with those of the original ABPBI membrane, suggestive of a promising polymer electrolyte for fuel cells at high temperature....

  20. Small, porous polyacrylate beads

    Science.gov (United States)

    Rembaum, Alan (Inventor); Yen, Shiao-Ping Siao (Inventor); Dreyer, William J. (Inventor)

    1976-01-01

    Uniformly-shaped, porous, round beads are prepared by the co-polymerization of an acrylic monomer and a cross-linking agent in the presence of 0.05 to 5% by weight of an aqueous soluble polymer such as polyethylene oxide. Cross-linking proceeds at high temperature above about 50.degree.C or at a lower temperature with irradiation. Beads of even shape and even size distribution of less than 2 micron diameter are formed. The beads will find use as adsorbents in chromatography and as markers for studies of cell surface receptors.

  1. Crosslinked, porous, polyacrylate beads

    Science.gov (United States)

    Rembaum, Alan (Inventor); Yen, Shiao-Ping S. (Inventor); Dreyer, William J. (Inventor)

    1977-01-01

    Uniformly-shaped, porous, round beads are prepared by the co-polymerization of an acrylic monomer and a cross-linking agent in the presence of 0.05 to 5% by weight of an aqueous soluble polymer such as polyethylene oxide. Cross-linking proceeds at high temperature above about 50.degree. C or at a lower temperature with irradiation. Beads of even shape and even size distribution of less than 2 micron diameter are formed. The beads will find use as adsorbents in chromatography and as markers for studies of cell surface receptors.

  2. Novel PVA/SiO2 Alkaline Micro-porous Polymer Electrolytes for Polymer Ni-MH Batteries%用于聚合物镍氢电池的新型PVA/SiO2碱性微孔聚合物电解质

    Institute of Scientific and Technical Information of China (English)

    陆霞; 吴仁香; 李波波; 朱云峰; 李李泉

    2013-01-01

    New po1y(vinyl alcohol)/silica (designated as PVA/SiO2) alkaline micro-porous polymer electrolytes (AMPEs)were prepared by soaking PVA/SiO2 micro-porous composite membranes,obtained by solution casting of PVA/PEG/SiO2 membrane in acetone solution,into an electrolyte solution of 6 mol/L KOH aqueous solution.The morphology and structure of PVA/SiO2 composite polymer membranes were characterized by scanning electron microscopy (SEM) and X-Ray diffraction (XRD).The SEM photographs showed that the nano-SiO2 filler content was a crucial issue for the well-dispersed and optimal-sized pores which could storage charge carrier durably.Meanwhile,the crystalline of PVA decreased effectively for a large number of crystal defects and free volume appeared in the interface of inorganic particles and polymer for the addition of nann-SiO2 filler.The electrochemical properties of the AMPEs were measured by the alternating current impedance (AC impedance) and the cyclic voltammetry (CV) techniques.The results indicated that the PVA/SiO2 AMPEs containing 5 ωnano-SiO2 filler exhibited good performances at room temperature,such as 1.62 × 10-2 S·cm-1 for ionic conductivity and 2.20 V for electrochemical stability window.What's more,we used the gravimetric method to obtain the electrolyte uptake of various PVA/SiO2 composite micro-porous polymer membranes.From the data,we learned that the maximum electrolyte uptake could reach to 102.7% and it had very relevance to the size of pores in PVA/SiO2 composite polymer membranes,andthen influenced the ionic conductivity.Each polymer Ni-MH battery was assembled by three parts:the new AMPE,Mg-based hydrogen storage alloy and the commercial sintered Ni(OH)2/NiOOH electrode,in which each part did for electrolyte and diaphragm,negative electrode and positive electrode,respectively.The cycle experiments of the batteries exhibited a high first-cycle discharge capacity of 613 mAh·g-1 and stable discharge capacities about 330 mAh·g-1 for the

  3. Biogenic Cracks in Porous Rock

    Science.gov (United States)

    Hemmerle, A.; Hartung, J.; Hallatschek, O.; Goehring, L.; Herminghaus, S.

    2014-12-01

    Microorganisms growing on and inside porous rock may fracture it by various processes. Some of the mechanisms of biofouling and bioweathering are today identified and partially understood but most emphasis is on chemical weathering, while mechanical contributions have been neglected. However, as demonstrated by the perseverance of a seed germinating and cracking up a concrete block, the turgor pressure of living organisms can be very significant. Here, we present results of a systematic study of the effects of the mechanical forces of growing microbial populations on the weathering of porous media. We designed a model porous medium made of glass beads held together by polydimethylsiloxane (PDMS), a curable polymer. The rheological properties of the porous medium, whose shape and size are tunable, can be controlled by the ratio of crosslinker to base used in the PDMS (see Fig. 1). Glass and PDMS being inert to most chemicals, we are able to focus on the mechanical processes of biodeterioration, excluding any chemical weathering. Inspired by recent measurements of the high pressure (~0.5 Mpa) exerted by a growing population of yeasts trapped in a microfluidic device, we show that yeast cells can be cultured homogeneously within porous medium until saturation of the porous space. We investigate then the effects of such an inner pressure on the mechanical properties of the sample. Using the same model system, we study also the complex interplay between biofilms and porous media. We focus in particular on the effects of pore size on the penetration of the biofilm within the porous sample, and on the resulting deformations of the matrix, opening new perspectives into the understanding of life in complex geometry. Figure 1. Left : cell culture growing in a model porous medium. The white spheres represent the grains, bonds are displayed in grey, and microbes in green. Right: microscopy picture of glass beads linked by PDMS bridges, scale bar: 100 μm.

  4. Investigation of the role of the micro-porous layer in polymer electrolyte fuel cells with hydrogen deuterium contrast neutron radiography.

    Science.gov (United States)

    Cho, Kyu Taek; Mench, Matthew M

    2012-03-28

    In this study, the high resolution hydrogen-deuterium contrast radiography method was applied to elucidate the impact of the micro-porous layer (MPL) on water distribution in the porous fuel cell media. At the steady state, deuterium replaced hydrogen in the anode stream, and the large difference in neutron attenuation of the D(2)O produced at the cathode was used to track the produced water. It was found that the water content peaked in the cathode-side diffusion media (DM) for the cell without MPL, but with an MPL on the anode and cathode DM, the peak water amount was pushed toward the anode, resulting in a relatively flattened water profile through components and demonstrating a liquid barrier effect. Additionally, the dynamic water behavior in diffusion media was analyzed to understand the effect of a MPL and operating conditions. The water content in the DM changed with applied current, although there is a significant amount of residual liquid content that does not appear to be part of capillary channels. The effect of the MPL on irreducible saturation in DM and cell performance was also investigated.

  5. Study of a novel porous gel polymer electrolyte based on thermoplastic polyurethane/poly(vinylidene fluoride-co-hexafluoropropylene) by electrospinning technique

    Science.gov (United States)

    Zhou, Ling; Cao, Qi; Jing, Bo; Wang, Xianyou; Tang, Xiaoli; Wu, Na

    2014-10-01

    A novel electrospun gel polymer electrolyte (GPE) consisting of thermoplastic polyurethane (TPU) and poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) is prepared and investigated. Its characteristics are investigated by scanning electron microscopy (SEM), thermal analysis (TGA). The GPE shows a maximum ionic conductivity of 4.1 × 10-3 S cm-1 with electrochemical stability up to 5.5 V versus Li+/Li at room temperature. In addition, it shows a first charge-discharge capacity of 168.8 mAh g-1 when the gel polymer electrolyte (GPE) is evaluated in a Li/PE/LiFePO4 cell under 0.1 C-rate at the first cycle. What's more, there is microscale attenuation (1%) in the 30 cycles of charge and discharge tests. The TPU/PVDF-HFP membrane has a high tensile strength (8.4 ± 0.3 MPa) and elongation at break (118.7 ± 0.2)%. With the outstanding electrochemical and mechanical performance, it is very suitable for application in polymer lithium ion batteries.

  6. Novel Polymer Microfluidics Technology for In Situ Planetary Exploration Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Los Gatos Research proposes to develop a novel microfluidic device that combines rigid monolithic porous polymer based micro-capillary electrochromatography...

  7. Sorption properties of porous melamine formaldehyde resins

    Science.gov (United States)

    Deryło-Marczewska, Anna; Goworek, Jacek; Kusak, Ryszard; Zgrajka, Wojciech

    2002-07-01

    Three types of melamine-formaldehyde porous sorbents were synthesized by using the fumed silica as an inorganic template. The changes in polymerization conditions lead to a differentiation of the porosity and surface area of these materials. This synthesis allowed preparing the materials of narrow pore size distributions with pore sizes over the range 2.8-6.8 nm, and specific surface areas up to 250 m 2/g. The analysis of pore structure was based on the comparison of nitrogen adsorption isotherms on a given porous sorbent and a standard nonporous polymer. Additionally the measurements of thermal stability and swelling of synthesized polymers were made. Adsorption of organic substances from aqueous solutions on porous polymers was also investigated.

  8. Ending Aging in Super Glassy Polymer Membranes

    Energy Technology Data Exchange (ETDEWEB)

    Lau, CH; Nguyen, PT; Hill, MR; Thornton, AW; Konstas, K; Doherty, CM; Mulder, RJ; Bourgeois, L; Liu, ACY; Sprouster, DJ; Sullivan, JP; Bastow, TJ; Hill, AJ; Gin, DL; Noble, RD

    2014-04-16

    Aging in super glassy polymers such as poly(trimethylsilylpropyne) (PTMSP), poly(4-methyl-2-pentyne) (PMP), and polymers with intrinsic microporosity (PIM-1) reduces gas permeabilities and limits their application as gas-separation membranes. While super glassy polymers are initially very porous, and ultra-permeable, they quickly pack into a denser phase becoming less porous and permeable. This age-old problem has been solved by adding an ultraporous additive that maintains the low density, porous, initial stage of super glassy polymers through absorbing a portion of the polymer chains within its pores thereby holding the chains in their open position. This result is the first time that aging in super glassy polymers is inhibited whilst maintaining enhanced CO2 permeability for one year and improving CO2/N-2 selectivity. This approach could allow super glassy polymers to be revisited for commercial application in gas separations.

  9. Composition suitable for decontaminating a porous surface contaminated with cesium

    Science.gov (United States)

    Kaminski, Michael D.; Finck, Martha R.; Mertz, Carol J.

    2010-06-15

    A method of decontaminating porous surfaces contaminated with water soluble radionuclides by contacting the contaminated porous surfaces with an ionic solution capable of solubilizing radionuclides present in the porous surfaces followed by contacting the solubilized radionuclides with a gel containing a radionuclide chelator to bind the radionuclides to the gel, and physically removing the gel from the porous surfaces. A dry mix is also disclosed of a cross-linked ionic polymer salt, a linear ionic polymer salt, a radionuclide chelator, and a gel formation controller present in the range of from 0% to about 40% by weight of the dry mix, wherein the ionic polymer salts are granular and the non cross-linked ionic polymer salt is present as a minor constituent.

  10. Porous silicon technology for integrated microsystems

    Science.gov (United States)

    Wallner, Jin Zheng

    With the development of micro systems, there is an increasing demand for integrable porous materials. In addition to those conventional applications, such as filtration, wicking, and insulating, many new micro devices, including micro reactors, sensors, actuators, and optical components, can benefit from porous materials. Conventional porous materials, such as ceramics and polymers, however, cannot meet the challenges posed by micro systems, due to their incompatibility with standard micro-fabrication processes. In an effort to produce porous materials that can be used in micro systems, porous silicon (PS) generated by anodization of single crystalline silicon has been investigated. In this work, the PS formation process has been extensively studied and characterized as a function of substrate type, crystal orientation, doping concentration, current density and surfactant concentration and type. Anodization conditions have been optimized for producing very thick porous silicon layers with uniform pore size, and for obtaining ideal pore morphologies. Three different types of porous silicon materials: meso porous silicon, macro porous silicon with straight pores, and macro porous silicon with tortuous pores, have been successfully produced. Regular pore arrays with controllable pore size in the range of 2mum to 6mum have been demonstrated as well. Localized PS formation has been achieved by using oxide/nitride/polysilicon stack as masking materials, which can withstand anodization in hydrofluoric acid up to twenty hours. A special etching cell with electrolytic liquid backside contact along with two process flows has been developed to enable the fabrication of thick macro porous silicon membranes with though wafer pores. For device assembly, Si-Au and In-Au bonding technologies have been developed. Very low bonding temperature (˜200°C) and thick/soft bonding layers (˜6mum) have been achieved by In-Au bonding technology, which is able to compensate the potentially

  11. Investigation of Ester- and Amide-Linker-Based Porous Organic Polymers for Carbon Dioxide Capture and Separation at Wide Temperatures and Pressures.

    Science.gov (United States)

    Ullah, Ruh; Atilhan, Mert; Anaya, Baraa; Al-Muhtaseb, Shaheen; Aparicio, Santiago; Patel, Hasmukh; Thirion, Damien; Yavuz, Cafer T

    2016-08-17

    Organic compounds, such as covalent organic framework, metal-organic frameworks, and covalent organic polymers have been under investigation to replace the well-known amine-based solvent sorption technology of CO2 and introduce the most efficient and economical material for CO2 capture and storage. Various organic polymers having different function groups have been under investigation both for low and high pressure CO2 capture. However, search for a promising material to overcome the issues of lower selectivity, less capturing capacity, lower mass transfer coefficient and instability in materials performance at high pressure and various temperatures is still ongoing process. Herein, we report synthesis of six covalent organic polymers (COPs) and their CO2, N2, and CH4 adsorption performances at low and high pressures up to 200 bar. All the presented COPs materials were characterized by using elemental analysis method, Fourier transform infrared spectroscopy (FTIR) and solid state nuclear magnetic resonance (NMR) spectroscopy techniques. Physical properties of the materials such as surface areas, pore volume and pore size were determined through BET analysis at 77 K. All the materials were tested for CO2, CH4, and N2 adsorption using state of the art equipment, magnetic suspension balance (MSB). Results indicated that, amide based material i.e. COP-33 has the largest pore volume of 0.2 cm(2)/g which can capture up to the maximum of 1.44 mmol/g CO2 at room temperature and at pressure of 10 bar. However, at higher pressure of 200 bar and 308 K ester-based compound, that is, COP-35 adsorb as large as 144 mmol/g, which is the largest gas capturing capacity of any COPs material obtained so far. Importantly, single gas measurement based selectivity of COP-33 was comparatively better than all other COPs materials at all condition. Nevertheless, overall performance of COP-35 rate of adsorption and heat of adsorption has indicated that this material can be considered for

  12. Synthesis, characterisation and adsorption properties of a porous copper(II) 3D coordination polymer exhibiting strong binding enthalpy and adsorption capacity for carbon dioxide.

    Science.gov (United States)

    Eckold, Pierre; Gee, William J; Hill, Matthew R; Batten, Stuart R

    2012-11-21

    The synthesis and characterisation of microporous coordination polymers containing copper(II) or cobalt(II) and 2-(pyridin-4-yl)malonaldehyde (Hpma) is described and the gas adsorption properties evaluated. Single-crystal X-ray structure determinations identified the structures as [M(pma)(2)]·2X (M = Cu, 1; Co, 2; X = MeOH, MeCN), which contain 3D networks with rutile topology and continuous 1D rectangular channels with diameters ranging from 3 to 4 Å. The materials exhibit low BET surface areas of 143 m(2) g(-1), but possess large capacities for carbon dioxide capture of 14.1 wt%. The small pore channels are shown to account for this, delivering a particularly strong binding enthalpy to adsorbed CO(2) of 38 kJ mol(-1), and a very large adsorption capacity relative to the low surface area.

  13. Porous carbons

    Indian Academy of Sciences (India)

    Satish M Manocha

    2003-02-01

    Carbon in dense as well as porous solid form is used in a variety of applications. Activated porous carbons are made through pyrolysis and activation of carbonaceous natural as well as synthetic precursors. Pyrolysed woods replicate the structure of original wood but as such possess very low surface areas and poor adsorption capacities. On activation, these exhibit increased adsorption volumes of 0.5–0.8 cm3 /gm and surface areas of 700–1800 m2 /gm depending on activation conditions, whether physical or chemical. Former carbons possess mixed pore size distribution while chemically activated carbons predominantly possess micropores. Thus, these carbons can be used for adsorption of wide distributions of molecules from gas to liquid. The molecular adsorption within the pores is due to single layer or multilayer molecule deposition at the pore walls and hence results in different types of adsorption isotherm. On the other hand, activated carbon fibres with controlled microporous structure and surface area in the range of 2500 m2 /gm can be developed by controlled pyrolysis and physical activation of amorphous carbon fibres. Active carbon fibres with unmatchable pore structure and surface characteristics are present and futuristic porous materials for a number of applications from pollution control to energy storage.

  14. Evaluation of a novel microextraction technique for aqueous samples: porous membrane envelope filled with multiwalled carbon nanotubes coated with molecularly imprinted polymer.

    Science.gov (United States)

    Tan, Feng; Deng, Minjie; Liu, Xue; Zhao, Hongxia; Li, Xiaona; Quan, Xie; Chen, Jingwen

    2011-03-01

    A novel microextraction technique based on membrane-protected multiwalled carbon nanotubes coated with molecularly imprinted polymer (MWCNTs-MIP) was developed. In this technique, MWCNTs-MIP were packed inside a polypropylene membrane envelope, which was then clamped onto a paper clip. For extraction, the packed membrane envelope was first impregnated with toluene and then placed in sample solutions. Target analytes in the solutions were first extracted into toluene in the membrane envelope, and were then extracted specifically onto the MWCNTs-MIP. After the extraction, target analytes were desorbed in methanol for liquid chromatography analysis. MWCNTs-MIP of prometryn were used as a model to demonstrate the feasibility of this novel microextraction technique. Factors affecting the extraction including organic solvent, stirring rate, extraction time, salt concentration, and pH were investigated. Under the optimized conditions, the limits of detection (a signal-to-noise ratio of 3) for the selected triazine herbicides were 0.08-0.38 μg/L. The prepared membrane envelope could be used at least 50 times. The developed method was used for the analysis of the triazines spiked in river water, wastewater, and liquid milk, with recoveries ranging from 79.3-97.4, 58.9-110.3 and 76.2-104.9%, respectively.

  15. 倒相法制备PVDF-HFP基复合微孔聚合物电解质%PVDF-HFP matrix complex micro-porous polymer electrolyte prepared by phase inversion method

    Institute of Scientific and Technical Information of China (English)

    刘辉; 顾大明; 白继元

    2012-01-01

    To improve the distribution properties of nanoparticles in the polymer electrolyte,micro-porous polymer electrolyte PVDF-HFP-SiO2(OP-10) was prepared with phase inversion method by adopting nano-sized SiO2 as the inorganic filler and OP-10 as dispersant.The morphology,crystal structure and electrochemical properties of the electrolyte were characterized by scanning electron microscope(SEM),X-ray diffraction(XRD),electrochemical impedance spectra(EIS).The results showed that the addition of nano-SiO2 suppressed the crystallinity of polymer electrolyte and enhanced the tensile intensity.The ionic conductivity was improved,the highest ionic conductivity(20 ℃) of the PVDF-HFP-SiO2(OP-10) polymer electrolyte was 4.90×10-3S·cm-1,with a high electrochemical stability window of 5.3 V,and the corresponding cation transference number was 0.83.The distribution of SiO2 and interfacial compatibility of nanometer particles were improved by the addition of OP-10.%为改善纳米粒子在聚合物电解质中的分散效果,采用倒相制膜法,以纳米SiO2为填料,以OP-10为分散剂,制备复合微孔聚偏氟乙烯-六氟丙烯基电解质PVDF-HFP-SiO2(OP-10).用SEM、XRD、交流阻抗法等测试手段对电解质的微观形貌、内部结构和电化学相关性能等进行表征,结果表明:SiO2的加入降低了聚合物电解质膜的结晶度,增强了电解质的拉伸强度,提高了PVDF-HFP-SiO2(OP-10)聚合物电解质的电导率,在20℃时,可达到4.90×10-3S.cm-1,电化学稳定窗口为5.3 V,电解质的离子迁移数为0.83.分散剂OP-10的加入改善了纳米SiO2与基质的界面相容性,改善了SiO2在基质中的分散度.

  16. 手性有机多孔材料在多相不对称催化中的应用研究进展%Advances in Chiral Porous Organic Polymers for Heterogeneous Asymmetric Catalysis

    Institute of Scientific and Technical Information of China (English)

    李延伟; 王昌安

    2015-01-01

    Porous organic polymers ( POPs) have become one of a frontier of the research in recent years . POPs include amorphous ( eg CMP, HCP, PIM, etc.) and crystalline ( eg COFs etc.) porous organic poly-mers.Due to their inherent porosity , large specific surface area , light weight and easy functionalization at the molecular level , POPs have recently received significant attention for potential applications in gas storage /sep-aration, organic photoelectric, sensoring and heterogeneous catalysis .Here, this review focuses on recent ad-vances of Chiral POPs in heterogeneous asymmetric catalysis .Currently , the research on the application of Chiral POPs for heterogeneous asymmetric catalysis is classified into two sections: a ) "bottom-up"embed-ding chiral metal-ligand catalyst into POPs for heterogeneous asymmetric catalysis; b) "bottom -up"em-bedding chiral organocatalyst into POPs for heterogeneous asymmetric organocatalyst .Benefiting from its struc-tural superiority , these functional POPs exhibit excellent catalytic activity .%近年来,有机多孔材料成为研究的前沿和热点领域之一。有机多孔材料POPs ( Porous Organic Polymers)包括非晶型有机多孔材料(比如CMP,HCP,PIM等)和晶型有机多孔材料(比如COFs等)。由于其具有优异的孔性质、较大的比表面积、稳定性好、重量轻以及易与功能化等诸多优点,有机多孔材料被广泛应用于气体存储分离、传感、有机光电和多相催化等重要领域。伴随着均相催化尤其是不对称催化的巨大发展,将有机多孔材料与手性催化剂结合起来构建手性有机多孔材料,并将其应用于多相不对称催化的研究越来越受到重视。目前,关于手性有机多孔材料在多相不对称催化领域应用的研究工作主要有两类:一类是通过“bottom-up”策略将手性配体-金属类催化剂嵌入有机多孔材料骨架来构建多相催化剂;一类是通过

  17. Three new three-dimensional organic-inorganic hybrid compounds based on PMo12O40(n-) (n = 3 or 4) polyanions and Cu(I)-pyrazine/Cu(I)-pyrazine-Cl porous coordination polymers.

    Science.gov (United States)

    Qi, Ming-Li; Yu, Kai; Su, Zhan-Hua; Wang, Chun-Xiao; Wang, Chun-Mei; Zhou, Bai-Bin; Zhu, Chun-Cheng

    2013-06-07

    Three new organic-inorganic hybrid compounds based on PMo12O40(n-) (n = 3 or 4) polyanions and Cu(I)-pz/Cu(I)-pz-Cl porous coordination polymers: [Cu(I)(pz)]3[PMo(VI)12O40] (1), [Cu(I)(pz)1.5]4[PMo(V)Mo(VI)11O40]·pz·2H2O (2), [Cu(I)3(pz)3Cl][Cu(I)2(pz)3(H2O)][PMo(V)Mo(VI)11O40] (3) (pz = pyrazine) have been hydrothermally prepared and characterized by elemental analysis, IR, TG, XRD, XPS and single-crystal X-ray diffraction. Compound 1 presents a three-dimensional Cu(I)-pz framework with cube-like chambers, into which PMo(VI)12O40(3-) Keggin ions are incorporated. Compound 2 shows a three-dimensional sandwich-like framework, and PMo(V)Mo(VI)11O40(4-) polyanions are located in the octagonal voids of every two-dimensional Cu(I)-pz 4(1)8(2) network structure. Compound 3 exhibits a two-dimensional Cl-bridged Cu(I)-pz-Cl double-layer structure, and two kinds of PMo(V)Mo(VI)11O40(4-) polyanions as bridging linkers connect two adjacent double-layers to form a three-dimensional organic-inorganic framework through Cu(I)-O bonds. Additionally, their electrochemical characters, electrocatalytic behaviors and solid state fluorescent properties at room temperature have been investigated in detail.

  18. polyMOFs: A Class of Interconvertible Polymer-Metal-Organic-Framework Hybrid Materials.

    Science.gov (United States)

    Zhang, Zhenjie; Nguyen, Ha Thi Hoang; Miller, Stephen A; Cohen, Seth M

    2015-05-18

    Preparation of porous materials from one-dimensional polymers is challenging because the packing of polymer chains results in a dense, non-porous arrangement. Herein, we demonstrate the remarkable adaptation of an amorphous, linear, non-porous, flexible organic polymer into a three-dimensional, highly porous, crystalline solid, as the organic component of a metal-organic framework (MOF). A polymer with aromatic dicarboxylic acids in the backbone functioned as a polymer ligand upon annealing with Zn(II), generating a polymer-metal-organic framework (polyMOF). These materials break the dogma that MOFs must be prepared from small, rigid ligands. Similarly, polyMOFs contradict conventional polymer chemistry by demonstrating that linear and amorphous polymers can be readily coaxed into a highly crystalline, porous, three-dimensional structure by coordination chemistry.

  19. Porous Ascend

    DEFF Research Database (Denmark)

    Riiber, Jacob; Tamke, Martin; Ramsgaard Thomsen, Mette

    2012-01-01

    The Porous Ascend project investigates how algorithmic and generative approaches allows for the utilization of complex, and by other means inaccessible, ways of devising the schema by which we arrange the parts of an architectural object. It does so by pursuing to physically realize a structure...... of folded elements, based on the concept of applying recursion to the geometry of the non-periodic Penrose tiling. Within this process the project explores questions regarding the making of bespoke digital design tools, digital production, material behaviour and assemblage strategies. The project points...... with an outside and an efficient distribution of specific material behaviour....

  20. Macroporous polymer foams by hydrocarbon templating

    OpenAIRE

    Shastri, Venkatram Prasad; Martin, Ivan; Langer, Robert

    2000-01-01

    Porous polymeric media (polymer foams) are utilized in a wide range of applications, such as thermal and mechanical insulators, solid supports for catalysis, and medical devices. A process for the production of polymer foams has been developed. This process, which is applicable to a wide range of polymers, uses a hydrocarbon particulate phase as a template for the precipitation of the polymer phase and subsequent pore formation. The use of a hydrocarbon template allows for enhanced control ov...

  1. Preparation and Gas Adsorption of Porous Materials from Molecular Precursors

    DEFF Research Database (Denmark)

    Hu, Xinming

    ABSTRACT This thesis deals with the synthesis of porous materials and their applications in gas adsorption. The thesis consists of eight chapters as follows: The first two chapters provide a brief introduction to porous materials and gas adsorption. Chapter 1 gives an overview of construction...... and characteristics of various porous materials, including activated carbons, zeolites, metal-organic frameworks (MOFs), covalent organic frameworks (COFs), and organic porous polymers (POPs). Chapter 2 briefly introduces gas adsorption theory, such as physical and chemical adsorption, adsorption isotherms...

  2. Synthesis and characterization of porous microspheres bearing pyrrolidone units

    Energy Technology Data Exchange (ETDEWEB)

    Maciejewska, M., E-mail: mmacieje@umcs.pl; Kołodyńska, D.

    2015-01-15

    Porous microspheres of glycydyl methacrylate (GMA) cross-linked with trimethylolpropane trimethacrylate (TRIM) were prepared with toluene as porogen by suspension-emulsion polymerization. With increasing molar ratio of the functional monomer to cross-linker, the epoxy group content increases significantly whereas the parameters of porous structure (specific surface area and total pore volume) decreases. In order to obtain adsorbents bearing functional groups the porous methacrylate network was modified by subsequent reaction with pyrrolidone. The materials were studied using elemental analysis, infrared spectroscopy, atomic force microscopy (AFM), attenuated total reflection (ATR) spectroscopy, Raman spectroscopy, thermal gravimetry. Additionally, polymers sorption capacity towards Cu(II) was investigated. - Highlights: • Porous microspheres with reactive epoxy group were synthesized. • Highly developed porous structure was created. • Pyrrolidone units were incorporated during ring–opening reaction. • Polymers sorption capacity towards Cu (II) was investigated.

  3. Methane storage in advanced porous materials.

    Science.gov (United States)

    Makal, Trevor A; Li, Jian-Rong; Lu, Weigang; Zhou, Hong-Cai

    2012-12-07

    The need for alternative fuels is greater now than ever before. With considerable sources available and low pollution factor, methane is a natural choice as petroleum replacement in cars and other mobile applications. However, efficient storage methods are still lacking to implement the application of methane in the automotive industry. Advanced porous materials, metal-organic frameworks and porous organic polymers, have received considerable attention in sorptive storage applications owing to their exceptionally high surface areas and chemically-tunable structures. In this critical review we provide an overview of the current status of the application of these two types of advanced porous materials in the storage of methane. Examples of materials exhibiting high methane storage capacities are analyzed and methods for increasing the applicability of these advanced porous materials in methane storage technologies described.

  4. Face-Centered-Cubic Nanostructured Polymer Foams

    Science.gov (United States)

    Cui, C.; Baughman, R. H.; Liu, L. M.; Zakhidov, A. A.; Khayrullin, I. I.

    1998-03-01

    Beautifully iridescent polymer foams having Fm-3m cubic symmetry and periodicities on the scale of the wavelength of light have been synthesized by the templating of porous synthetic opals. These fabrication processes involve the filling of porous SiO2 opals (with typical cubic lattice parameters of 250 nm) with either polymers or polymer precursors, polymerization of the precursors if necessary, and removal of the fcc array of SiO2 balls to provide an all-polymer structure. The structures of these foams are similar to periodic minimal surfaces, although the Gaussian curvature can have both positive and negative values. Depending upon whether the internal surfaces of the opal are polymer filled or polymer coated, the polymer replica has either one or two sets of independent channels. We fill these channels with semiconductors, metals, or superconductors to provide electronic and optical materials with novel properties dependent on the nanoscale periodicity.

  5. Controlled Morphology of Porous Polyvinyl Butyral Nanofibers

    Directory of Open Access Journals (Sweden)

    Daniela Lubasova

    2011-01-01

    Full Text Available A simple and effective method for the fabrication of porous nanofibers based on the solvent evaporation methods in one-step electrospinning process from the commercial polyvinyl butyral (PVB is presented. The obtained nanofibers are prevalently amorphous with diameters ranging from 150 to 4350 nm and specific surface area of approximately 2–20 m2/g. Pore size with irregular shape of the porous PVB fibers ranged approximately from 50 to 200 nm. The effects of polymer solution concentration, composition of the solvents mixture, and applied voltage on fiber diameter and morphology were investigated. The theoretical approach for the choice of poor and good solvents for PVB was explained by the application Hansen solubility parameter (HSP and two-dimensional graph. Three basic conditions for the production of porous PVB nanofibers were defined: (i application of good/poor solvent mixture for spinning solution, (ii differences of the evaporation rate between good/poor solvent, and (iii correct ratios of good/poor solvent (v/v. The diameter of prepared porous PVB fibers decreased as the polymer concentration was lowered and with higher applied voltage. These nanofiber sheets with porous PVB fibers could be a good candidate for high-efficiency filter materials in comparison to smooth fibers without pores.

  6. Polyphosphazine-based polymer materials

    Science.gov (United States)

    Fox, Robert V.; Avci, Recep; Groenewold, Gary S.

    2010-05-25

    Methods of removing contaminant matter from porous materials include applying a polymer material to a contaminated surface, irradiating the contaminated surface to cause redistribution of contaminant matter, and removing at least a portion of the polymer material from the surface. Systems for decontaminating a contaminated structure comprising porous material include a radiation device configured to emit electromagnetic radiation toward a surface of a structure, and at least one spray device configured to apply a capture material onto the surface of the structure. Polymer materials that can be used in such methods and systems include polyphosphazine-based polymer materials having polyphosphazine backbone segments and side chain groups that include selected functional groups. The selected functional groups may include iminos, oximes, carboxylates, sulfonates, .beta.-diketones, phosphine sulfides, phosphates, phosphites, phosphonates, phosphinates, phosphine oxides, monothio phosphinic acids, and dithio phosphinic acids.

  7. Controlled Morphology of Porous Polyvinyl Butyral Nanofibers

    OpenAIRE

    2011-01-01

    A simple and effective method for the fabrication of porous nanofibers based on the solvent evaporation methods in one-step electrospinning process from the commercial polyvinyl butyral (PVB) is presented. The obtained nanofibers are prevalently amorphous with diameters ranging from 150 to 4350 nm and specific surface area of approximately 2–20 m2/g. Pore size with irregular shape of the porous PVB fibers ranged approximately from 50 to 200 nm. The effects of polymer solution concentration,...

  8. Flow of polymer solutions through porous media

    NARCIS (Netherlands)

    Denys, K.F.J.

    2003-01-01

    These days leading oil and gas producing companies are investing increasing amounts of money into the development of non-fossil energy sources like wind-, solar-, biomass energy and forestry. On the other hand these companies are persisting in developing techniques to make energy recovery more effic

  9. Flow of polymer solutions through porous media

    NARCIS (Netherlands)

    Denys, K.F.J.

    2003-01-01

    These days leading oil and gas producing companies are investing increasing amounts of money into the development of non-fossil energy sources like wind-, solar-, biomass energy and forestry. On the other hand these companies are persisting in developing techniques to make energy recovery more

  10. Flow of polymer solutions through porous media

    NARCIS (Netherlands)

    Denys, K.F.J.

    2003-01-01

    These days leading oil and gas producing companies are investing increasing amounts of money into the development of non-fossil energy sources like wind-, solar-, biomass energy and forestry. On the other hand these companies are persisting in developing techniques to make energy recovery more effic

  11. Preparation and Gas Adsorption of Porous Materials from Molecular Precursors

    DEFF Research Database (Denmark)

    Hu, Xinming

    ABSTRACT This thesis deals with the synthesis of porous materials and their applications in gas adsorption. The thesis consists of eight chapters as follows: The first two chapters provide a brief introduction to porous materials and gas adsorption. Chapter 1 gives an overview of construction...... and characteristics of various porous materials, including activated carbons, zeolites, metal-organic frameworks (MOFs), covalent organic frameworks (COFs), and organic porous polymers (POPs). Chapter 2 briefly introduces gas adsorption theory, such as physical and chemical adsorption, adsorption isotherms...... rise to significant red-shift of absorption/emission and reduction of fluorescence lifetime and quantum yield Transition-metal-catalyzed and organolithium-mediated reactions provide polymers with only macroporous interparticle voids and thus very low surface areas (4−51 m2 g−1). Attempts have been also...

  12. Amine Functionalized Porous Network

    KAUST Repository

    Eddaoudi, Mohamed

    2015-05-28

    Amine groups can be introduced in porous materials by a direct (one pot) or post-synthetic modification (PSM) process on aldehyde groups, and the resulting porous materials have increased gas affinity.

  13. Polymer films

    Science.gov (United States)

    Granick, Steve; Sukhishvili, Svetlana A.

    2004-05-25

    A film contains a first polymer having a plurality of hydrogen bond donating moieties, and a second polymer having a plurality of hydrogen bond accepting moieties. The second polymer is hydrogen bonded to the first polymer.

  14. Polymer films

    Science.gov (United States)

    Granick, Steve; Sukhishvili, Svetlana A.

    2008-12-30

    A film contains a first polymer having a plurality of hydrogen bond donating moieties, and a second polymer having a plurality of hydrogen bond accepting moieties. The second polymer is hydrogen bonded to the first polymer.

  15. Nano-porous ultra-high specific surface ultrafine fibers

    Institute of Scientific and Technical Information of China (English)

    LI Xinsong; NIE Guangyu

    2004-01-01

    Nano-porous ultra-high specific surface ultrafine fibers are created by the method of "electrospinning-phase separation-leaching" (EPL) for the first time. First of all, polymer solutions of polyacrylonitrile (PAN) and polyvinylpyrrolidone (PVP) blends dissolved in co-solvent are electrospun to make ultrafine fibers when charged to high voltages. The incompatibility of PAN and PVP induces phase separation to form microdomains of PVP in the polymer blend ultrafine fibers. Then, PVP microdomains in the blend fibers are leached out in water, and porous PAN ultrafine fibers are obtained. Lastly, the surface and cross-section of the porous ultrafine fibers are observed in detail by field emission scanning electron microscope (FESEM), and the specific surface of the ultrafine fibers is measured by means of nitrogen absorption. With increasing the content of PVP, the specific surface area of the ultrafine fibers increases apparently. The specific surface area of the porous ultrafine fibers with the diameter of 2130 nm is more than 70 m2·g-1. The cross-section of the PAN porous ultrafine fibers after leaching of PVP microdomains from polymer blend fibers with the feed ratio of PAN/PVP of 10/20 shows the characteristic of porous structure with pore diameter of ca 30 nm according to FESEM photo.

  16. Tailored Porous Materials

    Energy Technology Data Exchange (ETDEWEB)

    BARTON,THOMAS J.; BULL,LUCY M.; KLEMPERER,WALTER G.; LOY,DOUGLAS A.; MCENANEY,BRIAN; MISONO,MAKOTO; MONSON,PETER A.; PEZ,GUIDO; SCHERER,GEORGE W.; VARTULI,JAMES C.; YAGHI,OMAR M.

    1999-11-09

    Tailoring of porous materials involves not only chemical synthetic techniques for tailoring microscopic properties such as pore size, pore shape, pore connectivity, and pore surface reactivity, but also materials processing techniques for tailoring the meso- and the macroscopic properties of bulk materials in the form of fibers, thin films and monoliths. These issues are addressed in the context of five specific classes of porous materials: oxide molecular sieves, porous coordination solids, porous carbons, sol-gel derived oxides, and porous heteropolyanion salts. Reviews of these specific areas are preceded by a presentation of background material and review of current theoretical approaches to adsorption phenomena. A concluding section outlines current research needs and opportunities.

  17. Thermal Spray Formation of Polymer Coatings

    Science.gov (United States)

    Coquill, Scott; Galbraith, Stephen L.; Tuss. Darren L.; Ivosevic, Milan

    2008-01-01

    This innovation forms a sprayable polymer film using powdered precursor materials and an in-process heating method. This device directly applies a powdered polymer onto a substrate to form an adherent, mechanically-sound, and thickness-regulated film. The process can be used to lay down both fully dense and porous, e.g., foam, coatings. This system is field-deployable and includes power distribution, heater controls, polymer constituent material bins, flow controls, material transportation functions, and a thermal spray apparatus. The only thing required for operation in the field is a power source. Because this method does not require solvents, it does not release the toxic, volatile organic compounds of previous methods. Also, the sprayed polymer material is not degraded because this method does not use hot combustion gas or hot plasma gas. This keeps the polymer from becoming rough, porous, or poorly bonded.

  18. [FTIR investigation of new polymer solid electrolytes].

    Science.gov (United States)

    Yang, Shu-ting; Chen, Hong-jun; Dong, Hong-yu; Jia, Jun-hua; Cao, Zhao-xia

    2004-04-01

    The conductivity of the porous polymer solid electrolyte blended with PVDF and PMMA, which was made by a micro-wave hot-cross-linking method, reached 2.05 x 10(-3) S x cm(-1) at room temperature. The polymer solid electrolyte was analyzed and investigated by FTIR. The results show that the PVDF, PMMA and LiClO4 in the polymer solid electrolyte were not simply blended, but certain kind of effect existed which was strengthened only when the polymer solid electrolyte came into being.

  19. Polymer fractionation

    Energy Technology Data Exchange (ETDEWEB)

    Hadermann, A. F.

    1985-04-09

    Soluble polymers are fractionated according to molecular weight by cryogenically comminuting the polymer and introducing the polymer particles, while still in the active state induced by cryogenic grinding, into a liquid having a solvent power selected to produce a coacervate fraction containing high molecular weight polymer species and a dilute polymer solution containing lower molecular weight polymer species. The coacervate may be physically separated from the solution and finds use in the production of antimisting jet fuels and the like.

  20. Biodegradable Polymers

    OpenAIRE

    Isabelle Vroman; Lan Tighzert

    2013-01-01

    Biodegradable materials are used in packaging, agriculture, medicine and other areas. In recent years there has been an increase in interest in biodegradable polymers. Two classes of biodegradable polymers can be distinguished: synthetic or natural polymers. There are polymers produced from feedstocks derived either from petroleum resources (non renewable resources) or from biological resources (renewable resources). In general natural polymers offer fewer advantages than synthetic polymers. ...

  1. How methylhydroxyethylcellulose (MHEC) influences drying in porous media

    NARCIS (Netherlands)

    Faiyas, A.P.A.; Erich, S.J.F.; Soestbergen, M. van; Huinink, H.P.; Adan, O.C.G.; Nijland, T.G.

    2015-01-01

    This article presents both an experimental as well as a theoretical study on the effect of MethylHy droxyEthylCellulose (MHEC) on drying in porous materials using Nuclear Magnetic Resonance Imaging (NMR). MHEC, a water soluble polymer, is normally added to glue mortars as a water retention agent in

  2. High-strength porous carbon and its multifunctional applications

    Science.gov (United States)

    Wojtowicz, Marek A; Rubenstein, Eric P; Serio, Michael A; Cosgrove, Joseph E

    2013-12-31

    High-strength porous carbon and a method of its manufacture are described for multifunctional applications, such as ballistic protection, structural components, ultracapacitor electrodes, gas storage, and radiation shielding. The carbon is produced from a polymer precursor via carbonization, and optionally by surface activation and post-treatment.

  3. Hierarchical Porous Structures

    Energy Technology Data Exchange (ETDEWEB)

    Grote, Christopher John [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-06-07

    Materials Design is often at the forefront of technological innovation. While there has always been a push to generate increasingly low density materials, such as aero or hydrogels, more recently the idea of bicontinuous structures has gone more into play. This review will cover some of the methods and applications for generating both porous, and hierarchically porous structures.

  4. Using ion-selective electrodes to study the drug release from porous cellulose matrices

    DEFF Research Database (Denmark)

    Vakili, Hossein; Genina, Natalja; Ehlers, Henrik;

    2012-01-01

    -polymer solutions were prepared with the model drugs, using different blend ratios of ethylcellulose (EC) and hydroxypropyl cellulose (HPC). Two different solid dosage forms were used. Polymer films were produced by solvent casting method and drug containing porous cellulose samples were prepared by depositing...... method \\r\

  5. Porous silicon gettering

    Energy Technology Data Exchange (ETDEWEB)

    Tsuo, Y.S.; Menna, P.; Al-Jassim, M. [National Renewable Energy Lab., Golden, CO (United States)] [and others

    1995-08-01

    We have studied a novel extrinsic gettering method that utilizes the very large surface areas, produced by porous silicon etch on both front and back surfaces of the silicon wafer, as gettering sites. In this method, a simple and low-cost chemical etching is used to generate the porous silicon layers. Then, a high-flux solar furnace (HFSF) is used to provide high-temperature annealing and the required injection of silicon interstitials. The gettering sites, along with the gettered impurities, can be easily removed at the end the process. The porous silicon removal process consists of oxidizing the porous silicon near the end the gettering process followed by sample immersion in HF acid. Each porous silicon gettering process removes up to about 10 {mu}m of wafer thickness. This gettering process can be repeated so that the desired purity level is obtained.

  6. Preparation of bioactive porous HA/PCL composite scaffolds

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, J.; Guo, L.Y.; Yang, X.B. [Key Laboratory of Advanced Technologies of Materials (Ministry of Education), School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Weng, J. [Key Laboratory of Advanced Technologies of Materials (Ministry of Education), School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China)], E-mail: jweng@swjtu.cn

    2008-12-30

    Porous hydroxyapatite (HA) bioceramic scaffold has been widely attracted the attention to act as a three-dimensional (3D) template for cell adhesion, proliferation, differentiation and thus promoting bone and cartilage regeneration because of its osteoinduction. However, the porous bioceramic scaffold is fragile so that it is not suitable to be applied in clinic for bone repair or replacement. Therefore, it is significant to improve the mechanical property of porous HA bioceramics while the interconnected structure is maintained for tissue ingrowth in vivo. In the present research, a porous composite scaffold composed of HA scaffold and polycaprolactone (PCL) lining was fabricated by the method of polymer impregnating to produce HA scaffold coated with PCL lining. Subsequently, the composite scaffolds were deposited with biomimetic coating for improving the bioactivity. The HA/PCL composite scaffolds with improved mechanical property and bioactivity is expected to be a promising bone substitute in tissue engineering applications.

  7. Preparation of bioactive porous HA/PCL composite scaffolds

    Science.gov (United States)

    Zhao, J.; Guo, L. Y.; Yang, X. B.; Weng, J.

    2008-12-01

    Porous hydroxyapatite (HA) bioceramic scaffold has been widely attracted the attention to act as a three-dimensional (3D) template for cell adhesion, proliferation, differentiation and thus promoting bone and cartilage regeneration because of its osteoinduction. However, the porous bioceramic scaffold is fragile so that it is not suitable to be applied in clinic for bone repair or replacement. Therefore, it is significant to improve the mechanical property of porous HA bioceramics while the interconnected structure is maintained for tissue ingrowth in vivo. In the present research, a porous composite scaffold composed of HA scaffold and polycaprolactone (PCL) lining was fabricated by the method of polymer impregnating to produce HA scaffold coated with PCL lining. Subsequently, the composite scaffolds were deposited with biomimetic coating for improving the bioactivity. The HA/PCL composite scaffolds with improved mechanical property and bioactivity is expected to be a promising bone substitute in tissue engineering applications.

  8. Physical characterization of hydroxyapatite porous scaffolds for tissue engineering

    Energy Technology Data Exchange (ETDEWEB)

    Teixeira, S., E-mail: smsilva@ineb.up.pt [INEB - Instituto de Engenharia Biomedica, Divisao de Biomateriais, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto (Portugal); Universidade do Porto, Faculdade de Engenharia, Departamento de Engenharia Metalurgica e Materiais, Porto (Portugal); Rodriguez, M.A.; Pena, P.; De Aza, A.H.; De Aza, S. [Instituto de Ceramica y Vidrio, CSIC, 28049-Cantoblanco, Madrid (Spain); Ferraz, M.P. [INEB - Instituto de Engenharia Biomedica, Divisao de Biomateriais, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto (Portugal); Faculdade de Ciencias da Saude da Universidade Fernando Pessoa, Rua Carlos da Maia, 296, 4200-150 Porto (Portugal); Monteiro, F.J. [INEB - Instituto de Engenharia Biomedica, Divisao de Biomateriais, Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto (Portugal); Universidade do Porto, Faculdade de Engenharia, Departamento de Engenharia Metalurgica e Materiais, Porto (Portugal)

    2009-06-01

    The present study refers to the preparation and characterization of porous hydroxyapatite scaffolds to be used as matrices for bone regeneration or as specific release vehicles. Ceramics are widely used for bone tissue engineering purposes and in this study, hydroxyapatite porous scaffolds were produced using the polymer replication method. Polyurethane sponges were used as templates and impregnated with a ceramic slurry at different ratios, and sintered at 1300 deg. C following a specific thermal cycle. The characteristics of the hydroxyapatite porous scaffolds and respective powder used as starting material, were investigated by using scanning electron microscopy, particle size distribution, X-ray diffraction, Fourier transformed infrared spectroscopy and compressive mechanical testing techniques. It was possible to produce highly porous hydroxyapatite scaffolds presenting micro and macropores and pore interconnectivity.

  9. Conducting polyheterocycle composites based on porous hosts

    Science.gov (United States)

    Park, J. S.; Ruckenstein, E.

    1992-02-01

    Conducting composites based on porous substrates (cotton fiber, non-woven polypropylene mat and porous crosslinked polystyrene) have been prepared by a two step imbibition technique. First, the substrate was imbibed with a solution of monomer (pyrrole or bithiophene) in acetonitrile, followed by partial drying. Subsequently, the substrate was again imbibed, this time with an oxidant dissolved in a suitable solvent. The polymerization of the monomer inside the host in the presence of the oxidant and the doping of the polymer with the oxidant leads to the conducting composite. The highly hydrophobic and porous crosslinked polystyrene, prepared by the concentrated emulsion polymerization method, is the most efficient. The solvent employed for the oxidant plays a major role. A FeCl3-methanol system and porous crosslinked polystyrene lead to conductivities of polythiophene and polypyrrole based composites of 3.63 and 0.65 S/cm, respectively. Copper perchlorate and iron perchlorate are also suitable oxidants. The environmental and thermal stabilities of polypyrrole based composites are lower than those of polythiophene based composites. The thermal stability of polypyrrole based composites can be enhanced by including a small amount of an organic antioxidant, such as amides or substituted phenols, in the composite.

  10. Deformation of Linked Polymer Coils

    Institute of Scientific and Technical Information of China (English)

    董朝霞; 李明远; 吴肇亮; 林梅钦

    2003-01-01

    Linked polymer solution (LPS) is defined as the solution of linked polymer coils (LPCs) dispersed in water, composed of low concentration partially hydrolyzed polyacrylamide (HPAM) and aluminum citrate (crosslinker). In the work, the conformational changes of LPCs under different conditions were investigated by the methods of membrane filtering under low pressure, dynamic light scattering and core flooding experiments. The results showed that in some conditions the LPCs could be compressed mechanically to 1/158.5 of their original volume because of relatively lower HPAM cross-linking. The hydration property of LPCs was similar to that of normal polymer coils. The deformation of LPCs was more restricted than that of ordinary polymer coils under the flow shear stress or the shift of hydration equilibrium caused in the variation of the electrolyte concentration which is responsible for the effective plugging in the throats of porous media when LPCs are used for deep diverting.

  11. MULTILAYER POROUS COMPOSITE FROM WASTE GLASS FOR WATER FILTRATION

    Directory of Open Access Journals (Sweden)

    M. P. Aji

    2015-07-01

    Full Text Available Multilayer porous composite have been produced through the heating process at temperature T=700oC for 2.5 h. Single layered porous composite was made with a varied mass percentage of from PEG polymer  1% to 10%. Double-layered porous composite were made by the arrangement of porosity (4:3%, (4:2% and (3:2%, while the three-layers porous composite have an arrangement (4:3:2%. Performance of multilayer porous composite for water filtration with pollutants of methylene blue 100 ppm was estimated from the absorbance spectrum. Rejection of methylene blue pollutants from single layered porous composite increases when the fraction of PEG polymer tend to be smaller in the matrix. Meanwhile, the double layered porous composite has a degradation of methylene blue pollutants are better than one layer. Triple layered porous composite have good performance for the water filtration where all the pollutants of methylene blue be able to be filtered.   Komposit pori berlapis telah dihasilkan dengan proses pemanasan pada temperatur T=700oC selama 2.5 jam. Komposit pori satu lapis dibuat dengan variasi persen massa polimer PEG 1% hingga 10%. Komposit pori dua lapis dibuat dengan susunan porositas (4:3%, (4:2% dan (3:2%, sedangkan komposit pori tiga lapis memiliki susunan porositas (4:3:2%. Kinerja komposit pori berlapis untuk filter air dengan polutan methylene blue 100 ppm diestimasi dari spektrum absorbansi. Rejeksi polutan methylene blue dari komposit pori satu lapis meningkat saat fraksi polimer PEG cenderung lebih kecil dalam matrik komposit. Sedangkan, komposit pori dua lapis memiliki kemampuan untuk degradasi polutan methylene blue yang lebih baik dari satu lapis. Komposit pori tiga lapis memiliki kinerja yang baik untuk filter air dimana seluruh polutan methylene blue mampu disaring. 

  12. Biodegradable Polymers

    Directory of Open Access Journals (Sweden)

    Isabelle Vroman

    2009-04-01

    Full Text Available Biodegradable materials are used in packaging, agriculture, medicine and other areas. In recent years there has been an increase in interest in biodegradable polymers. Two classes of biodegradable polymers can be distinguished: synthetic or natural polymers. There are polymers produced from feedstocks derived either from petroleum resources (non renewable resources or from biological resources (renewable resources. In general natural polymers offer fewer advantages than synthetic polymers. The following review presents an overview of the different biodegradable polymers that are currently being used and their properties, as well as new developments in their synthesis and applications.

  13. Polymer electronics

    CERN Document Server

    Hsin-Fei, Meng

    2013-01-01

    Polymer semiconductor is the only semiconductor that can be processed in solution. Electronics made by these flexible materials have many advantages such as large-area solution process, low cost, and high performance. Researchers and companies are increasingly dedicating time and money in polymer electronics. This book focuses on the fundamental materials and device physics of polymer electronics. It describes polymer light-emitting diodes, polymer field-effect transistors, organic vertical transistors, polymer solar cells, and many applications based on polymer electronics. The book also disc

  14. 水溶性聚合物在多孔介质中动态滞留量研究%Research on dynamic hold-up of water-soluble polymer in porous medium

    Institute of Scientific and Technical Information of China (English)

    李宜强; 曲成永

    2011-01-01

    During the oil extraction process, liquid hold-up is one of the key factors in influencing the effect of polymer flooding.Directing at the application conditions limitation of water- soluble polymer on site, the dynamical hold up law of polyacrylamide solution in artificial core was conducted with starch-cadmium iodide colorimetry in this paper, and the effect of kaolin clay, surfactant on liquid hold up was inspected. The results show that the retention volume of polymer was decreased when surfactant have been contained in the solution, on the other hand, the exist of kaolin clay in solution raised retention volume of polymer in the core, and the hold- up volume was increased with the increasing of kaolin content. When both the surfactant and polymer were included in solution, these two would react to each other which resulted in competitive adsorption in rock surface and reduced their effective content. So, in order to enhance the flooding efficiency, the concentration of surfactant and polymer should adjust based on the contribution of the two to EOR and their differences of adsorption and liquid hold up.%滞留量是影响聚合物驱油效果的关键因素之一.针对水溶性聚合物在现场应用条件的局限性,利用淀粉一碘化锅比色法研究了聚丙烯酰胺水溶液在人造均质岩心中的动态滞留规律,并考察了高岭土、表面活性剂对其滞留量产生的影响.结果表明,溶液中含有表面活性剂时,聚合物的滞留量减少;高岭土的存在使聚合物在岩心中的滞留量增加,随着高岭土含量的增加,滞留量增大.表活剂与聚合物同时存在时,二者之间会发生一定的相互作用,在岩石表面会产生竞争吸附,造成其有效含量降低,因此要保证驱油效率的提高,应当依据二者时提高采收率的贡献及吸附滞留的差异对其浓度进行适当的调高.

  15. Stochastic porous media equations

    CERN Document Server

    Barbu, Viorel; Röckner, Michael

    2016-01-01

    Focusing on stochastic porous media equations, this book places an emphasis on existence theorems, asymptotic behavior and ergodic properties of the associated transition semigroup. Stochastic perturbations of the porous media equation have reviously been considered by physicists, but rigorous mathematical existence results have only recently been found. The porous media equation models a number of different physical phenomena, including the flow of an ideal gas and the diffusion of a compressible fluid through porous media, and also thermal propagation in plasma and plasma radiation. Another important application is to a model of the standard self-organized criticality process, called the "sand-pile model" or the "Bak-Tang-Wiesenfeld model". The book will be of interest to PhD students and researchers in mathematics, physics and biology.

  16. Nano/macro porous bioactive glass scaffold

    Science.gov (United States)

    Wang, Shaojie

    Bioactive glass (BG) and ceramics have been widely studied and developed as implants to replace hard tissues of the musculo-skeletal system, such as bones and teeth. Recently, instead of using bulk materials, which usually do not degrade rapidly enough and may remain in the human body for a long time, the idea of bioscaffold for tissue regeneration has generated much interest. An ideal bioscaffold is a porous material that would not only provide a three-dimensional structure for the regeneration of natural tissue, but also degrade gradually and, eventually be replaced by the natural tissue completely. Among various material choices the nano-macro dual porous BG appears as the most promising candidate for bioscaffold applications. Here macropores facilitate tissue growth while nanopores control degradation and enhance cell response. The surface area, which controls the degradation of scaffold can also be tuned by changing the nanopore size. However, fabrication of such 3D structure with desirable nano and macro pores has remained challenging. In this dissertation, sol-gel process combined with spinodal decomposition or polymer sponge replication method has been developed to fabricate the nano-macro porous BG scaffolds. Macropores up to 100microm are created by freezing polymer induced spinodal structure through sol-gel transition, while larger macropores (>200um) of predetermined size are obtained by the polymer sponge replication technique. The size of nanopores, which are inherent to the sol-gel method of glass fabrication, has been tailored using several approaches: Before gel point, small nanopores are generated using acid catalyst that leads to weakly-branched polymer-like network. On the other hand, larger nanopores are created with the base-catalyzed gel with highly-branched cluster-like structure. After the gel point, the nanostructure can be further modified by manipulating the sintering temperature and/or the ammonia concentration used in the solvent

  17. Unconventional High Density Vertically Aligned Conducting Polymer

    Science.gov (United States)

    2014-08-21

    CNTs also provide a porous scaffold to deposit PEDOT via CVD. To fabricate PEDOT/ A-CNT electrodes, the conducting polymer was conformally deposited on...250μm long A-CNTs using oCVD, varying thickness from few to ten nm by controlling deoposition and polymerization times. Electron microscopy

  18. Non-conjugate potential-stepping phenothiazine and phenoxazine based polymer hole-transport material for dye-sensitized solar cells & increasing void space in porous titanium dioxide: To study diffusion properties of a cobalt mediator

    Science.gov (United States)

    Persson, Kristoffer

    As energy demands increase so has the search for alternative sources of energy. Although, fossil fuels have proven useful in energy production, they are also detrimental due to the negative impact on our environment. Considering the current alternative energy sources, such as wind, hydroelectric, biofuels, etc, one source of alternative energy shines above the rest, solar energy. Solar energy provides a possible solution to the energy demands of our modern world with little effect on the environment. The only waste produced from the solar cell industry is from producing and recycling the cells. After production, solar cells require no resources to function other than solar radiation, and no waste is produced. The sun has been powering life on this planet for billions of years, and bombards the earth with 3x1024 J of energy per year. Only 0.02% of this energy is currently needed to power the world, thus making the sun a viable solution to energy demands, while decreasing current pollution issues. This thesis focuses on dye sensitized solar cell (DSSCs), in particular, the Grätzel cell, which incorporates thin films of TiO2 as the semiconductor, DSSC's work very similarly to a battery, but instead of using chemical energy to drive electrons through the circuit, it uses photons. Several issues have arisen with these types of solar cells and their use in the modern world. One particular problem is that the iodide/triiodide (I -/I3-) mediator, which currently produces the most efficient DSSCs, is corrosive and volatile. To address this and other issues, a conductive phenothiazine (PTZ) and phenoxazine (POZ) based polymer is hypothesized to be a suitable replacement for the mediator and solvent by acting as a charge separator and hole transport material, without any volatile or corrosive problems. This polymer would hypothetically function similarly to proposed electron transport in DNA. When charges are injected into a DNA strand they are transferred through

  19. Nitrogen-rich porous adsorbents for CO2 capture and storage.

    Science.gov (United States)

    Li, Pei-Zhou; Zhao, Yanli

    2013-08-01

    The construction of physical or chemical adsorbents for CO2 capture and sequestration (CCS) is a vital technology in the interim period on the way towards a sustainable low-carbon future. The search for efficient materials to satisfy the increasing demand for CCS has become extremely important. Porous materials, including porous silica, porous carbons, and newly developed metal-organic frameworks and porous organic polymers, possessing regular and well-defined porous geometry and having a high surface area and pore volume, have been widely studied for separations on laboratory scale. On account of the dipole-quadrupole interactions between the polarizable CO2 molecule and the accessible nitrogen site, the investigations have indicated that the incorporation of accessible nitrogen-donor groups into the pore walls of porous materials can improve the affinity to CO2 and increase the CO2 uptake capacity and selectivity. The CO2 -adsorption process based on solid nitrogen-rich porous adsorbents does generally not require heating of a large amount of water (60-70 wt%) for regeneration, while such a heating approach cannot be avoided in the regeneration of amine-based solution absorption processes. Thus, nitrogen-rich porous adsorbents show good regeneration properties without sacrificing high separation efficiency. As such, nitrogen-rich porous materials as highly promising CO2 adsorbents have been broadly fabricated and intensively investigated. This Focus Review highlights recent significant advances in nitrogen-rich porous materials for CCS.

  20. PHOTOREFRACTIVE POLYMERS

    NARCIS (Netherlands)

    Morichere, D; Malliaras, G.G; Krasnikov, V.V.; Bolink, H.J; Hadziioannou, G

    1995-01-01

    The use of polymers as photorefractive materials offers many advantages : flexibility in synthesis, doping, processing and low cost. The required functionalities responsible for photorefractivity, namely charge generation, transport, trapping and linear electrooptic effect are given in the polymer w

  1. PHOTOREFRACTIVE POLYMERS

    NARCIS (Netherlands)

    Morichere, D; Malliaras, G.G; Krasnikov, V.V.; Bolink, H.J; Hadziioannou, G

    1995-01-01

    The use of polymers as photorefractive materials offers many advantages : flexibility in synthesis, doping, processing and low cost. The required functionalities responsible for photorefractivity, namely charge generation, transport, trapping and linear electrooptic effect are given in the polymer w

  2. Field Study of Infiltration Capacity Reduction of Porous Mixture Surfaces

    Directory of Open Access Journals (Sweden)

    Luis A. Sañudo-Fontaneda

    2014-03-01

    Full Text Available Porous surfaces have been used all over the world in source control techniques to minimize flooding problems in car parks. Several studies highlighted the reduction in the infiltration capacity of porous mixture surfaces after several years of use. Therefore, it is necessary to design and develop a new methodology to quantify this reduction and to identify the hypothetical differences in permeability between zones within the same car park bay due to the influence of static loads in the parked vehicles. With this aim, nine different zones were selected in order to check this hypothesis (four points under the wheels of a standard vehicle and five points between wheels. This article presents the infiltration capacity reduction results, using the LCS permeameter, of Polymer-Modified Porous Concrete (9 bays and Porous Asphalt (9 bays surfaces in the University of Cantabria Campus parking area (Spain 5 years after their construction. Statistical analysis methodology was proposed for assessing the results. Significant differences were observed in permeability and reduction in infiltration capacity in the case of porous concrete surfaces, while no differences were found for porous asphalt depending on the measurement zone.

  3. Polymer Brushes

    NARCIS (Netherlands)

    Vos, de W.M.; Kleijn, J.M.; Keizer, de A.; Cosgrove, T.; Cohen Stuart, M.A.

    2010-01-01

    A polymer brush can be defined as a dense array of polymers end-attached to an interface that stretch out into the surrounding medium. Polymer brushes have been investigated for the past 30 years and have shown to be an extremely useful tool to control interfacial properties. This review is intended

  4. Colorometric detection of water using MOF-polymer films and composites

    Energy Technology Data Exchange (ETDEWEB)

    Allendorf, Mark D.; Talin, Albert Alec

    2016-05-24

    A method including exposing a mixture of a porous metal organic framework (MOF) and a polymer to a predetermined molecular species, wherein the MOF has an open metal site for the predetermined molecular species and the polymer has a porosity for the predetermined molecular species; and detecting a color change of the MOF in the presence of the predetermined molecular species. A method including combining a porous metal organic framework (MOF) and a polymer, wherein the MOF has an open metal site for a predetermined molecular species and the polymer has a porosity for the predetermined molecular species. An article of manufacture including a mixture of a porous metal organic framework (MOF) and a polymer, wherein the MOF has an open metal site for a predetermined molecular species and the polymer has a porosity for the predetermined molecular species.

  5. Colorometric detection of water using MOF-polymer films and composites

    Science.gov (United States)

    Allendorf, Mark D.; Talin, Albert Alec

    2016-05-24

    A method including exposing a mixture of a porous metal organic framework (MOF) and a polymer to a predetermined molecular species, wherein the MOF has an open metal site for the predetermined molecular species and the polymer has a porosity for the predetermined molecular species; and detecting a color change of the MOF in the presence of the predetermined molecular species. A method including combining a porous metal organic framework (MOF) and a polymer, wherein the MOF has an open metal site for a predetermined molecular species and the polymer has a porosity for the predetermined molecular species. An article of manufacture including a mixture of a porous metal organic framework (MOF) and a polymer, wherein the MOF has an open metal site for a predetermined molecular species and the polymer has a porosity for the predetermined molecular species.

  6. A microporous gel electrolyte based on poly(vinylidene fluoride-co-hexafluoropropylene)/fully cyanoethylated cellulose derivative blend for lithium-ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Ren Zhong [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China); Liu Yuyan [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China)], E-mail: liuyy@hit.edu.cn; Sun Kening; Zhou Xiaoliang; Zhang Naiqing [Science Reseach Center, Harbin Institute of Technology, Harbin 150001 (China)

    2009-02-15

    A gel polymer electrolyte based on the blend of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and fully cyanoethylated cellulose derivative (DH-4-CN) was prepared and characterized. Thermal, mechanical, swelling, liquid electrolyte retention and electrochemical properties, as well as microstructures of the prepared polymer electrolytes, were investigated using thermogravimetric analysis, electrochemical impedance spectroscopy, linear sweep voltammetry, and scanning electron microscopy. The results showed that the addition of DH-4-CN could obviously improve the conductivity of PVDF-HFP based electrolyte. The maximum ionic conductivity of 4.36 mS cm{sup -1} at 20 deg. C can be obtained for PVDF-HFP/DH-4-CN 14:1 in the presence of 1 M LiPF{sub 6} in EC and DMC (1:1, w/w). The dry blend membranes exhibit excellent thermal behavior. All the blend electrolytes are electrochemically stable up to about 4.8 V vs. Li/Li{sup +} for all compositions. The results reveal that the composite polymer electrolyte qualifies as a potential application in lithium-ion battery.

  7. Method of porous diamond deposition on porous silicon

    Science.gov (United States)

    Baranauskas, Vitor; Peterlevitz, Alfredo C.; Chang, Dahge C.; Durrant, Steven F.

    2001-12-01

    In this paper, we discuss the experimental results of the fabrication of porous diamond/porous silicon and porous diamond structures by chemical vapor deposition of diamond over a skeleton of porous silicon, replicating the porous surface geometry around the Si pores and also creating new porous diamond structures. Scanning electron microscopy (SEM) revealed that the diamond nuclei are deposited on the top of the porous silicon skeleton, forming isolated grains in the first nucleation stages, and then growing like the usual structure of most ceramic materials, making a self-sustained porous diamond structure. Raman spectroscopy revealed that the diamond films are of good quality, close to that of diamond films grown on crystalline silicon.

  8. The Research of Biomedical Intelligent Polymer Materials

    Institute of Scientific and Technical Information of China (English)

    ZHANG Zhi-bin; CHEN Yuan-wei; TANG Chang-wei; QIU Kai; LUO Juan; XU Cheng-yin; WAN Chang-xiu

    2004-01-01

    The properties of biomedical intelligent polymer materials can be changed obviously when there is a little physical or chemical change caused by external condition. They are in the forms of solids, solutions and the polymers on the surface of carrier, and include water solution of hydrophilic polymers, cross-linking hydrophilic polymers(i.e. hydrogels) and the polymers on the surface of carrier. The environmental stimulating factors are temperature, pH value, composition of solution, ionic intention, light intention, electric field, stress field and magnetic field etc.. The properties of intelligent polymer are those of phase, photics, mechanics, electric field, surface energy,reaction ratio, penetrating ratio and recognition etc..Stimulation-response of intelligent water-soluble polymerWater-soluble intelligent polymer can be separated out from solution under special external condition. It can be used as the switch of temperature or pH indicator. When water-soluble intelligent polymer is mixed with soluble-enzyme matter or cell suspension, the polymer can bring phase separation and react with soluble-enzyme matter or cell membrane through accepting some external stimulation. Other water-soluble intelligent polymer is that can make the main chemical group of some natural biomolecular recognition sequence section to arrange on skeleton of polymer at random. It is the same ratio as natural biomolecules.Stimulation-response of intelligent polymer of carrier surface Intelligent polymer can be fixed on the surface of solid polymer carrier through chemical grafting or physical adsorption. When the external conditions are changed, the thickness, humidity and electric field of the surface layer will be changed. Intelligent polymer can be preparated the permanence switch by precipitating into the hole of porous surface, and it can control on-off state of the hole. When protein or cell interacts with intelligent polymer surface to be placed in to open or close, they can be

  9. A review: fabrication of porous polyurethane scaffolds.

    Science.gov (United States)

    Janik, H; Marzec, M

    2015-03-01

    The aim of tissue engineering is the fabrication of three-dimensional scaffolds that can be used for the reconstruction and regeneration of damaged or deformed tissues and organs. A wide variety of techniques have been developed to create either fibrous or porous scaffolds from polymers, metals, composite materials and ceramics. However, the most promising materials are biodegradable polymers due to their comprehensive mechanical properties, ability to control the rate of degradation and similarities to natural tissue structures. Polyurethanes (PUs) are attractive candidates for scaffold fabrication, since they are biocompatible, and have excellent mechanical properties and mechanical flexibility. PU can be applied to various methods of porous scaffold fabrication, among which are solvent casting/particulate leaching, thermally induced phase separation, gas foaming, emulsion freeze-drying and melt moulding. Scaffold properties obtained by these techniques, including pore size, interconnectivity and total porosity, all depend on the thermal processing parameters, and the porogen agent and solvents used. In this review, various polyurethane systems for scaffolds are discussed, as well as methods of fabrication, including the latest developments, and their advantages and disadvantages.

  10. Functional Nanoporous Polymers from Block Copolymer Precursors

    DEFF Research Database (Denmark)

    Guo, Fengxiao

    functionalities remains a great challenge due to the limitation of available polymer synthesis and the nanoscale confinement of the porous cavities. The main topic of this thesis is to develop methods for fabrication of functional nanoporous polymers from block copolymer precursors. A method has been developed...... functional nanoporous polymers based on nanoporous 1,2- polybuatdiene 1,2-PB, which is derived from a 1,2-PB-b-PDMS diblock copolymer precursor. As a result, nanoporous 1,2-PB with pores decorated of polyacrylates, sulfonated polymers and poly(ethylene glycol) are created. A method of vapor phase deposition...... has also been generated to obtain nanoporous polymers with functional coatings on pore walls. Vapor phase polymerization of pyrrole is performed to incorporate an ultra thin film of polypyrrole into nanoporous 1,2-PB. The preliminary test shows that nanoporous 1,2-PB gains conductivity. Generally...

  11. Effects of Forming Pressure on the Porosity of Polyimide Porous Materials

    Institute of Scientific and Technical Information of China (English)

    PU Yu-ping; L(U) Guang-shu; ZHAO Peng; XIAO Han-cheng

    2008-01-01

    Based on a series of experiments,the theory of relationship between normal pressure and pores' characters fit for polymer was set up for the first time.On the study of relation between normal pressure and porosity,experience model of polyimide porous materials was proposed which is similar to the traditional experience model of the metal porous material.While being pressed.polyimide was found soon to come into elastoplastic deformation progress in this paper,so the theory model of metal porous material based on Hooker's law Was not fit for the polymer any more.A new elasto-plastic deformation and exhausting model is proposed which shows better agreement with polymer material's pressing process.

  12. Porous block nanofiber composite filters

    Energy Technology Data Exchange (ETDEWEB)

    Ginley, David S.; Curtis, Calvin J.; Miedaner, Alexander; Weiss, Alan J.; Paddock, Arnold

    2016-08-09

    Porous block nano-fiber composite (110), a filtration system (10) and methods of using the same are disclosed. An exemplary porous block nano-fiber composite (110) includes a porous block (100) having one or more pores (200). The porous block nano-fiber composite (110) also includes a plurality of inorganic nano-fibers (211) formed within at least one of the pores (200).

  13. Development and characterization of porous functionalized collagen scaffolds for delivery of FGF-2

    OpenAIRE

    Pokholenko Ia. O.; Chetyrkina M. D.; Dubey L. V.; Dubey I. Ya.; Moshynets O. V.; Sheludko E. V.; Shpylova S. P.; Degtiarova M. I.; Kordium V. A.

    2014-01-01

    Aim. To develop the porous functionalized collagen scaffold for the delivery of FGF-2 and studying its properties in vitro and in vivo. Methods. Porous collagen scaffolds were prepared by freeze- drying collagen I solutions containing the polymer developed on the basis of cross-linked modified heparin. The scaffolds have been analyzed by SEM, AFM and SCLM. The angiogenic activity of these scaffolds loaded with FGF-2 was tested in a CAM assay. Results. The data obtained by SEM and SCLM analysi...

  14. A New Method of Hierarchical Porous HAP/Polyacrylic Acid Hydrogel Composite by in Situ Precipitation

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    1IntroductionBiological hardtissues ,such as the bone andteeth,are composite fabricated by nano-structure porous hydrox-yapatite (HAP) and collagenfibers . Herein,the investi-gation of newinorganic/organic composite nanomaterialsisa rapidly developing and expanding area of research withtremendous potential for biomedical applications .Becauseof applicationof pre HAPis verylimited duetoits brittle-ness ,soit is of most importance to synthesize nano-com-posites of porous HAP/organic polymer in order to havego...

  15. Porous silicon gettering

    Energy Technology Data Exchange (ETDEWEB)

    Tsuo, Y.S.; Menna, P.; Pitts, J.R. [National Renewable Energy Lab., Golden, CO (United States)] [and others

    1996-05-01

    The authors have studied a novel extrinsic gettering method that uses the large surface areas produced by a porous-silicon etch as gettering sites. The annealing step of the gettering used a high-flux solar furnace. They found that a high density of photons during annealing enhanced the impurity diffusion to the gettering sites. The authors used metallurgical-grade Si (MG-Si) prepared by directional solidification casing as the starting material. They propose to use porous-silicon-gettered MG-Si as a low-cost epitaxial substrate for polycrystalline silicon thin-film growth.

  16. 4-Nitrobenzene Grafted in Porous Silicon: Application to Optical Lithography.

    Science.gov (United States)

    Tiddia, Mariavitalia; Mula, Guido; Sechi, Elisa; Vacca, Annalisa; Cara, Eleonora; De Leo, Natascia; Fretto, Matteo; Boarino, Luca

    2016-12-01

    In this work, we report a method to process porous silicon to improve its chemical resistance to alkaline solution attacks based on the functionalization of the pore surface by the electrochemical reduction of 4-nitrobenzendiazonium salt. This method provides porous silicon with strong resistance to the etching solutions used in optical lithography and allows the fabrication of tailored metallic contacts on its surface. The samples were studied by chemical, electrochemical, and morphological methods. We demonstrate that the grafted samples show a resistance to harsh alkaline solution more than three orders of magnitude larger than that of pristine porous silicon, being mostly unmodified after about 40 min. The samples maintained open pores after the grafting, making them suitable for further treatments like filling by polymers. Optical lithography was performed on the functionalized samples, and electrochemical characterization results are shown.

  17. Porous Biodegradable Metals for Hard Tissue Scaffolds: A Review

    Directory of Open Access Journals (Sweden)

    A. H. Yusop

    2012-01-01

    Full Text Available Scaffolds have been utilized in tissue regeneration to facilitate the formation and maturation of new tissues or organs where a balance between temporary mechanical support and mass transport (degradation and cell growth is ideally achieved. Polymers have been widely chosen as tissue scaffolding material having a good combination of biodegradability, biocompatibility, and porous structure. Metals that can degrade in physiological environment, namely, biodegradable metals, are proposed as potential materials for hard tissue scaffolding where biodegradable polymers are often considered as having poor mechanical properties. Biodegradable metal scaffolds have showed interesting mechanical property that was close to that of human bone with tailored degradation behaviour. The current promising fabrication technique for making scaffolds, such as computation-aided solid free-form method, can be easily applied to metals. With further optimization in topologically ordered porosity design exploiting material property and fabrication technique, porous biodegradable metals could be the potential materials for making hard tissue scaffolds.

  18. 己二酸/酚醛树脂共聚炭化制备多孔炭材料及其电性能研究%Preparation of Porous Carbon by Polymer Blending of Phenolic Resin and Adipic Diacid

    Institute of Scientific and Technical Information of China (English)

    夏笑虹; 刘洪波; 黄衍瑞; 杨丽; 石磊

    2011-01-01

    Porous carbons used for electric double layer capacitors (EDLCs) were prepared by chemical blending of phenolic resin (PF) and adipic diacid (DA). Chemical reaction of PF with diacid is manifested by a shift of carbonyl stretching peak of diacid to a higher frequency in FT-IR spectra and a higher decomposition temperature of diacid in TG curves. The influences of the ratio of vv(DA) to vv(PF) on pore structure, adsorption behavior and capacity performance were investigated. The specific surface area and total pore volume increase with the ratio of w(DA) to w(PF) at first and then decrease, reach the maximum at the value of w(PF)/w(DA), which are 550 cm2/g and 0.27 cm3/g, respectively. When the porous carbon used for the electrodes of electrochemical double layer capacitor (EDLC), a satisfied specific capacitances of 145 F/g in 30 wt% KOH aqueous electrolytes is acquired and the capacitance maintenance achieve 70% while the current density enlarged 50 times.%以酚醛树脂(PF)为炭前驱体,己二酸(DA)为致孔链段,利用聚合物共聚炭化法制备双电层电容器用多孔炭材料:通过红外和热重分析证实己二酸与酚醛树脂发生了化学反应,DA以链段或支链的形式存在于酚醛树脂固化体系中,并在后续炭化过程中热解逸出.氮气吸附分析表明酚醛树脂固化体系中的DA起到了一定的造孔作用,随着DA加入量增加,多孔炭比表面积先增大后减小,当w(PF)/w(DA )=3∶1时所得多孔炭的比表面积为550 cm2/g,孔容为0.27 cm3/g.采用直流充放电法、交流阻抗法和循环伏安法测定以上述多孔炭为电极材料的双电层电容器的电化学性能,结果表明:w(PF)/w(DA)=3:1时制得的多孔炭电极在30% KOH电解液中比电容为145 F/g,电流密度增大50倍,比电容保持率达到70%.

  19. Effect of Spin-Crossover-Induced Pore Contraction on CO2–Host Interactions in the Porous Coordination Polymers [Fe(pyrazine)M(CN)4] (M = Ni, Pt)

    Energy Technology Data Exchange (ETDEWEB)

    Culp, Jeffrey T; Chen, De-Li; Liu, Jinchen; Chirdon, Danielle; Kauffman, Kristi; Goodman, Angela; Johnson, J Karl

    2013-02-01

    Variable-temperature in situ ATR-FTIR spectra are presented for the porous spin-crossover compounds [Fe(pyrazine)Ni(CN)4] and [Fe(pyrazine)Pt(CN)4] under CO2 pressures of up to 8 bar. Significant shifts in the ν3 and ν2 IR absorption bands of adsorbed CO2 are observed as the host materials undergo transition between low- and high-spin states. Computational models used to determine the packing arrangement of CO2 within the pore structures show a preferred orientation of one of the adsorbed CO2 molecules with close O=C=O···H contacts with the pyrazine pillar ligands. The interaction is a consequence of the commensurate distance of the inter-pyrazine separations and the length of the CO2 molecule, which allows the adsorbed CO2 to effectively bridge the pyrazine pillars in the structure. The models were used to assign the distinct shifts in the IR absorption bands of the adsorbed CO2 that arise from changes in the O=C=O···H contacts that strengthen and weaken in correlation with changes in the Fe–N bond lengths as the spin state of Fe changes. The results indicate that spin-crossover compounds can function as a unique type of flexible sorbent in which the pore contractions associated with spin transition can affect the strength of CO2–host interactions.

  20. Thermoforming techniques for manufacturing porous scaffolds for application in 3D cell cultivation.

    Science.gov (United States)

    Borowiec, Justyna; Hampl, Jörg; Gebinoga, Michael; Elsarnagawy, Tarek; Elnakady, Yasser A; Fouad, Hassan; Almajhadi, Fahd; Fernekorn, Uta; Weise, Frank; Singh, Sukhdeep; Elsarnagawy, Dief; Schober, Andreas

    2015-04-01

    Within the scientific community, there is an increasing demand to apply advanced cell cultivation substrates with increased physiological functionalities for studying spatially defined cellular interactions. Porous polymeric scaffolds are utilized for mimicking an organ-like structure or engineering complex tissues and have become a key element for three-dimensional (3D) cell cultivation in the meantime. As a consequence, efficient 3D scaffold fabrication methods play an important role in modern biotechnology. Here, we present a novel thermoforming procedure for manufacturing porous 3D scaffolds from permeable materials. We address the issue of precise thermoforming of porous polymer foils by using multilayer polymer thermoforming technology. This technology offers a new method for structuring porous polymer foils that are otherwise available for non-porous polymers only. We successfully manufactured 3D scaffolds from solvent casted and phase separated polylactic acid (PLA) foils and investigated their biocompatibility and basic cellular performance. The HepG2 cell culture in PLA scaffold has shown enhanced albumin secretion rate in comparison to a previously reported polycarbonate based scaffold with similar geometry.

  1. Porous multi-component material for the capture and separation of species of interest

    Energy Technology Data Exchange (ETDEWEB)

    Addleman, Raymond S.; Chouyyok, Wilaiwan; Li, Xiaohong S.; Cinson, Anthony D.; Gerasimenko, Aleksandr A

    2016-06-21

    A method and porous multi-component material for the capture, separation or chemical reaction of a species of interest is disclosed. The porous multi-component material includes a substrate and a composite thin film. The composite thin film is formed by combining a porous polymer with a nanostructured material. The nanostructured material may include a surface chemistry for the capture of chemicals or particles. The composite thin film is coupled to the support or device surface. The method and material provides a simple, fast, and chemically and physically benign way to integrate nanostructured materials into devices while preserving their chemical activity.

  2. A Perspective on the Synthesis, Purification, and Characterization of Porous Organic Cages.

    Science.gov (United States)

    Briggs, Michael E; Cooper, Andrew I

    2017-01-10

    Porous organic cages present many opportunities in functional materials chemistry, but the synthetic challenges for these molecular solids are somewhat different from those faced in the areas of metal-organic frameworks, covalent-organic frameworks, or porous polymer networks. Here, we highlight the practical methods that we have developed for the design, synthesis, and characterization of imine porous organic cages using CC1 and CC3 as examples. The key points are transferable to other cages, and this perspective should serve as a practical guide to researchers who are new to this field.

  3. Optical and electrical properties of blue-light polyfluorence/porous silicon composites

    Institute of Scientific and Technical Information of China (English)

    ZHONG Fu-ru; SHI Wei; LV Xiao-yi; JIA Zhen-hong

    2011-01-01

    Optical and electrical properties of composites formed by mixing porous silicon (PS) and poly (9, 9- diocty-2, 7-fiuoreneco4, 4'-butoxydiphenyl) (PFP) have been studied by Fourier transform-infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and photoluminescence (PL) spectroscopy. The optical spectra show that porous silicon is incorporated into the polymer without significant change in the polymer properties. The FT-IR spectroscopy has detected the existence of specific interactions, which may be attributed to non-conjugated alkoxy segment. By fitting the current-voltage (Ⅰ-Ⅴ)curve of PFP/PS structure with the modified standard equation, the n factor and I0 are determined.

  4. Formulation of porous poly(lactic-co-glycolic acid) microparticles by electrospray deposition method for controlled drug release

    Energy Technology Data Exchange (ETDEWEB)

    Hao, Shilei; Wang, Yazhou; Wang, Bochu, E-mail: wangbc2000@126.com; Deng, Jia; Zhu, Liancai; Cao, Yang

    2014-06-01

    In the present study, the electrospray deposition was successfully applied to prepare the porous poly(lactic-co-glycolic acid) (PLGA) microparticles by one-step processing. Metronidazole was selected as the model drug. The porous PLGA microparticles had high drug loading and low density, and the porous structure can be observed by scanning electron microscope (SEM) and transmission electron microscopy (TEM). The production time has been shortened considerably compared with that of the traditional multi-emulsion method. In addition, no chemical reaction occurred between the drug and polymer in the preparation of porous microparticles, and the crystal structure of drug did not change after entrapment into the porous microparticles. The porous microparticles showed a sustained release in the simulated gastric fluid, and the release followed non-Fickian or case II transport. Furthermore, porous microparticles showed a slight cytotoxicity in vitro. The results indicated that electrospray deposition is a good technique for preparation of porous microparticles, and the low-density porous PLGA microparticles has a potential for the development of gastroretentive systems or for pulmonary drug delivery. - Highlights: • The porous PLGA microparticles were successfully prepared by the electrospray deposition method at one step. • The porous microparticles had high loading capacity and low density. • The microparticle showed a sustained release in the simulated gastric liquid. • The microparticles showed a slight cytotoxicity in vitro.

  5. Prediction and improvement of the lifetime of polymer pressure casting moulds

    NARCIS (Netherlands)

    Dortmans, L.J.M.G.; Fischer, H.R.; Nelissen, R.

    2002-01-01

    The lifetime of porous polymer moulds used for pressure casting of sanitaryware has been analysed, modelled and improved. The mechanical behaviour of the existing porous PMMA mould material was analysed using mechanical tests to assess the lifetime under cyclic loading. The relevant stress levels we

  6. STAR POLYMERS

    OpenAIRE

    Ch. von Ferber; Yu.Holovatch

    2002-01-01

    It is our great pleasure to present a collection of papers devoted to theoretical, numerical, and experimental studies in the field of star polymers. Since its introduction in the early 80-ies, this field has attracted increasing interest and has become an important part of contemporary polymer physics. While research papers in this field appear regularly in different physical and chemical journals, the present collection is an attempt to join together the studies of star polymers showing the...

  7. Surfactant-templating of Ordered Mesoporous Polymers and Carbons

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    1 Results Ordered mesoporous materials possess enormous potential for many high-tech applications[1] such as bioreactors, microelectrophoresis, thermal insulation and catalysts. In general, organic porous materials can be prepared by phase-separation and hard templating approach such as those employing colloidal particles[2]. However, due to the volume contraction and swelling, and the structured defects formed during template removal, most of the resulting porous polymer structures are disordered with ...

  8. Polymer Chemistry

    Science.gov (United States)

    Williams, Martha; Roberson, Luke; Caraccio, Anne

    2010-01-01

    This viewgraph presentation describes new technologies in polymer and material chemistry that benefits NASA programs and missions. The topics include: 1) What are Polymers?; 2) History of Polymer Chemistry; 3) Composites/Materials Development at KSC; 4) Why Wiring; 5) Next Generation Wiring Materials; 6) Wire System Materials and Integration; 7) Self-Healing Wire Repair; 8) Smart Wiring Summary; 9) Fire and Polymers; 10) Aerogel Technology; 11) Aerogel Composites; 12) Aerogels for Oil Remediation; 13) KSC's Solution; 14) Chemochromic Hydrogen Sensors; 15) STS-130 and 131 Operations; 16) HyperPigment; 17) Antimicrobial Materials; 18) Conductive Inks Formulations for Multiple Applications; and 19) Testing and Processing Equipment.

  9. 0.4Ah class graphite/LiMn{sub 2}O{sub 4} lithium-ion battery prototypes

    Energy Technology Data Exchange (ETDEWEB)

    Appetecchi, Giovanni Battista; Prosini, Pier Paolo [ENEA, IDROCOMB, C.R. Casaccia, Via Anguillarese 301, 00060 Rome (Italy)

    2005-08-26

    0.4Ah lithium-ion battery prototypes, developed within a national project devoted to development of power sources for consumer applications, have been fabricated and tested. A novel, intrinsically porous, PVdF-HFP/MgO composite separator, capable to be hot-laminated onto PVDF-HFP-based electrodes without losing its ability to retain liquid electrolyte, was developed. The devices were assembled by direct lamination of the components, namely graphite anode tapes, PVDF-HFP/MgO separators and LiMn{sub 2}O{sub 4} cathode films. The prototypes, formed by a stack of 12 single cells connected in parallel, need no external pressure to maintain contact between the layers. The battery performance was evaluated in terms of capacity, cycle life, energy and power density at different rates. The capability of prototypes to uptake liquid electrolyte was also investigated. The results have indicated the feasibility to scale-up lithium-ion cells to manufacture 0.4Ah class battery prototypes showing good cycling performance. (author)

  10. 0.4 Ah class graphite/LiMn 2O 4 lithium-ion battery prototypes

    Science.gov (United States)

    Appetecchi, Giovanni Battista; Prosini, Pier Paolo

    0.4 Ah lithium-ion battery prototypes, developed within a national project devoted to development of power sources for consumer applications, have been fabricated and tested. A novel, intrinsically porous, PVdF-HFP/MgO composite separator, capable to be hot-laminated onto PVDF-HFP-based electrodes without losing its ability to retain liquid electrolyte, was developed. The devices were assembled by direct lamination of the components, namely graphite anode tapes, PVDF-HFP/MgO separators and LiMn 2O 4 cathode films. The prototypes, formed by a stack of 12 single cells connected in parallel, need no external pressure to maintain contact between the layers. The battery performance was evaluated in terms of capacity, cycle life, energy and power density at different rates. The capability of prototypes to uptake liquid electrolyte was also investigated. The results have indicated the feasibility to scale-up lithium-ion cells to manufacture 0.4 Ah class battery prototypes showing good cycling performance.

  11. Poly(acrylic acid) coating induced 2-line ferrihydrite nanoparticle transport in saturated porous media

    Science.gov (United States)

    Xiang, Aishuang; Yan, Weile; Koel, Bruce E.; Jaffé, Peter R.

    2013-07-01

    Iron oxide and iron nanoparticles (NPs) have been used effectively for environmental remediation, but are limited in their applications by strong retention in groundwater-saturated porous media. For example, delivery of NPs to large groundwater reservoirs would require large numbers of injection wells. To address this problem, we have explored polymer coatings as a surface engineering strategy to enhance transport of oxide nanoparticles in porous media. We report here on our studies of 2-line ferrihydrite NPs and the influence of poly (acrylic acid) (PAA) polymer coatings on the colloidal stability and transport in natural sand-packed column tests simulating flow in groundwater-saturated porous media. Measurements were also made of zeta potential, hydrodynamic diameter, and polymer adsorption and desorption properties. The coated NPs have a diameter range of 30-500 nm. We found that NP transport was improved by PAA coating and that the transport properties could be tuned by adjusting the polymer concentration. Our results demonstrate that a high stability of oxide particles and improved transport can be achieved in groundwater-saturated porous media by introducing negatively charged polyelectrolytes and optimizing polymer concentrations.

  12. Poly(acrylic acid) coating induced 2-line ferrihydrite nanoparticle transport in saturated porous media

    Energy Technology Data Exchange (ETDEWEB)

    Xiang, Aishuang [Princeton University, Chemical and Biological Engineering Department (United States); Yan, Weile [Texas Tech University, Civil and Environmental Engineering (United States); Koel, Bruce E., E-mail: bkoel@princeton.edu [Princeton University, Chemical and Biological Engineering Department (United States); Jaffe, Peter R., E-mail: jaffe@princeton.edu [Princeton University, Civil and Environmental Engineering Department (United States)

    2013-07-15

    Iron oxide and iron nanoparticles (NPs) have been used effectively for environmental remediation, but are limited in their applications by strong retention in groundwater-saturated porous media. For example, delivery of NPs to large groundwater reservoirs would require large numbers of injection wells. To address this problem, we have explored polymer coatings as a surface engineering strategy to enhance transport of oxide nanoparticles in porous media. We report here on our studies of 2-line ferrihydrite NPs and the influence of poly (acrylic acid) (PAA) polymer coatings on the colloidal stability and transport in natural sand-packed column tests simulating flow in groundwater-saturated porous media. Measurements were also made of zeta potential, hydrodynamic diameter, and polymer adsorption and desorption properties. The coated NPs have a diameter range of 30-500 nm. We found that NP transport was improved by PAA coating and that the transport properties could be tuned by adjusting the polymer concentration. Our results demonstrate that a high stability of oxide particles and improved transport can be achieved in groundwater-saturated porous media by introducing negatively charged polyelectrolytes and optimizing polymer concentrations.

  13. Polymers & People

    Science.gov (United States)

    Lentz, Linda; Robinson, Thomas; Martin, Elizabeth; Miller, Mary; Ashburn, Norma

    2004-01-01

    Each Tuesday during the fall of 2002, teams of high school students from three South Carolina counties conducted a four-hour polymer institute for their peers. In less than two months, over 300 students visited the Charleston County Public Library in Charleston, South Carolina, to explore DNA, nylon, rubber, gluep, and other polymers. Teams of…

  14. Preparation and characterization of monodisperse large-porous silica microspheres as the matrix for protein separation.

    Science.gov (United States)

    Xia, Hongjun; Wan, Guangping; Zhao, Junlong; Liu, Jiawei; Bai, Quan

    2016-11-04

    High performance liquid chromatography (HPLC) is a kind of efficient separation technology and has been used widely in many fields. Micro-sized porous silica microspheres as the most popular matrix have been used for fast separation and analysis in HPLC. In this paper, the monodisperse large-porous silica microspheres with controllable size and structure were successfully synthesized with polymer microspheres as the templates and characterized. First, the poly(glycidyl methacrylate-co-ethyleneglycol dimethacrylate) microspheres (PGMA-EDMA) were functionalized with tetraethylenepentamine (TEPA) to generate amino groups which act as a catalyst in hydrolysis of tetraethyl orthosilicate (TEOS) to form Si-containing low molecular weight species. Then the low molecular weight species diffused into the functionalized PGMA-EDMA microspheres by induction force of the amino groups to form polymer/silica hybrid microspheres. Finally, the organic polymer templates were removed by calcination, and the large-porous silica microspheres were obtained. The compositions, morphology, size distribution, specific surface area and pore size distribution of the porous silica microspheres were characterized by infrared analyzer, scanning-electron microscopy, dynamic laser scattering, the mercury intrusion method and thermal gravimetric analysis, respectively. The results show that the agglomeration of the hybrid microspheres can be overcome when the templates were functionalized with TEPA as amination reagent, and the yield of 95.7% of the monodisperse large-porous silica microspheres can be achieved with high concentration of polymer templates. The resulting large-porous silica microspheres were modified with octadecyltrichlorosilane (ODS) and the chromatographic evaluation was performed by separating the proteins and the digest of BSA. The baseline separation of seven kinds of protein standards was achieved, and the column delivered a better performance when separating BSA digests

  15. Graded/Gradient Porous Biomaterials

    Directory of Open Access Journals (Sweden)

    Xigeng Miao

    2009-12-01

    Full Text Available Biomaterials include bioceramics, biometals, biopolymers and biocomposites and they play important roles in the replacement and regeneration of human tissues. However, dense bioceramics and dense biometals pose the problem of stress shielding due to their high Young’s moduli compared to those of bones. On the other hand, porous biomaterials exhibit the potential of bone ingrowth, which will depend on porous parameters such as pore size, pore interconnectivity, and porosity. Unfortunately, a highly porous biomaterial results in poor mechanical properties. To optimise the mechanical and the biological properties, porous biomaterials with graded/gradient porosity, pores size, and/or composition have been developed. Graded/gradient porous biomaterials have many advantages over graded/gradient dense biomaterials and uniform or homogenous porous biomaterials. The internal pore surfaces of graded/gradient porous biomaterials can be modified with organic, inorganic, or biological coatings and the internal pores themselves can also be filled with biocompatible and biodegradable materials or living cells. However, graded/gradient porous biomaterials are generally more difficult to fabricate than uniform or homogenous porous biomaterials. With the development of cost-effective processing techniques, graded/gradient porous biomaterials can find wide applications in bone defect filling, implant fixation, bone replacement, drug delivery, and tissue engineering.

  16. Fabrication of Porous Materials from Natural/Synthetic Biopolymers and Their Composites

    OpenAIRE

    Udeni Gunathilake T.M. Sampath; Yern Chee Ching; Cheng Hock Chuah; Johari J. Sabariah; Pai-Chen Lin

    2016-01-01

    Biopolymers and their applications have been widely studied in recent years. Replacing the oil based polymer materials with biopolymers in a sustainable manner might give not only a competitive advantage but, in addition, they possess unique properties which cannot be emulated by conventional polymers. This review covers the fabrication of porous materials from natural biopolymers (cellulose, chitosan, collagen), synthetic biopolymers (poly(lactic acid), poly(lactic-co-glycolic acid)) and the...

  17. Convection in Porous Media

    CERN Document Server

    Nield, Donald A

    2013-01-01

    Convection in Porous Media, 4th Edition, provides a user-friendly introduction to the subject, covering a wide range of topics, such as fibrous insulation, geological strata, and catalytic reactors. The presentation is self-contained, requiring only routine mathematics and the basic elements of fluid mechanics and heat transfer. The book will be of use not only to researchers and practicing engineers as a review and reference, but also to graduate students and others entering the field. The new edition features approximately 1,750 new references and covers current research in nanofluids, cellular porous materials, strong heterogeneity, pulsating flow, and more. Recognized as the standard reference in the field Includes a comprehensive, 250-page reference list Cited over 2300 times to date in its various editions Serves as an introduction for those entering the field and as a comprehensive reference for experienced researchers Features new sections on nanofluids, carbon dioxide sequestration, and applications...

  18. Porous Electrode Studies.

    Science.gov (United States)

    1980-07-01

    representation and analysis for their observed current distributions. Simonsson won the young author’s award of the Electrochemical Society for his paper...and T. Katan, Proc. Symp. Energy Storage and Conversion, the Electrochemical Society 77-6, 770 (1977) The optimum thickness of porous electrodes is...Chloride Electrodes; Surface Morphology on Charging and Dis- charging," T. Katan, S. Szpak, and D. N. Bennion, The Electrochemical Society , 143rd National

  19. Platelets self-assemble into porous nacre during freeze casting.

    Science.gov (United States)

    Hunger, Philipp M; Donius, Amalie E; Wegst, Ulrike G K

    2013-03-01

    Nacre possesses a remarkable combination of mechanical properties. Its high stiffness, strength and toughness are attributed to a highly aligned structure of aragonite platelets "glued" together by a small fraction (∼5vol%) of polymer; theoretically it can be described by a shear-lag model of staggered tensile elements between which loads are transferred via shear. Despite extensive research, it has not been possible yet to manufacture this aligned structure as a bulk material of considerable volume with a fast and easy production process. Particularly porous materials would benefit from enhanced wall material properties to compensate for performance loss due to their high porosity. An important application for such porous materials are tissue scaffolds for bone substitution. Bone, like nacre, exhibits excellent mechanical properties, particularly an exceptionally high toughness, because of its composite structure of hydroxyapatite platelets aligned in a ∼35vol% polymer matrix. Through the freeze casting process, which results in a fast and straightforward self-assembly of platelet-shaped particles during directional solidification, highly porous bulk materials with nacre-like cell walls can now be created. This porous nacre outperforms by a factor of 1.5-4 in terms of stiffness, strength and toughness materials that have the same amount of porosity but do not exhibit the nacre-like microarchitecture. The self-assembly process presented in this study thus has tremendous potential for the creation of highly porous, yet mechanically strong tissue scaffolds for low or medium load bearing bone substitute materials. Due to the versatility of the freeze casting process, materials with a self-assembled cell wall structure can be created from high-aspect ratio particles of all material classes. This enables material optimization for a great variety of applications such as impact protection, filtration, catalysis, energy generation and storage, in addition to those with

  20. Biopolymer system for permeability modification in porous media

    Energy Technology Data Exchange (ETDEWEB)

    Stepp, A.K.; Bryant, R.S.; Llave, F.M. [BMD-Oklahoma, Inc., Bartlesville, OK (United States)] [and others

    1995-12-31

    New technologies are needed to reduce the current high rate of well abandonment. Improved sweep efficiency, reservoir conformance, and permeability modification can have a significant impact on oil recovery processes. Microorganisms can be used to selectively plug high-permeability zones to improve sweep efficiency and impart conformance control. Studies of a promising microbial system for polymer production were conducted to evaluate reservoir conditions in which this system would be effective. Factors which can affect microbial growth and polymer production include salinity, pH, temperature, divalent ions, presence of residual oil, and rock matrix. Flask tests and coreflooding experiments were conducted to optimize and evaluate the effectiveness of this system. Nuclear magnetic resonance imaging (NMRI) was used to visualize microbial polymer production in porous media. Changes in fluid distribution within the pore system of the core were detected.

  1. Porous poly(methylmethacrylate and poly(methylmethacrylate-co-acrylamide

    Directory of Open Access Journals (Sweden)

    Nikolić Ljubiša

    2006-01-01

    Full Text Available The characteristics of two types of porous polymers: poly(methyl methacrylate and copolymers of methyl methacrylate and acrylamide were investigated in this study. Poly(methyl methacrylate was synthesized in suspension, using ethylene glycol dimethacrylate as the cross-linking agent, poly(vinyl pyrrolidone as the protective colloid, and benzoyl peroxide as the initiator. The synthesis of poly(methyl methacrylate-co-acrylamide was initiated in emulsion in the presence of dioctyl sulfosuccinate sodium salt, followed by a sol-gel process, and completely reacted to the solid state. Potassium persulfate was used as the initiator, and tetramethylol glycoluril as the cross-linking agent. Both types of syntheses were carried out in the presence of ethyl acetate. The porosity, specific surface and distribution of the pore sizes of the obtained polymers were determined by mercury porosimetry. The polymers were used as inert carriers for the immobilization of enzymes and whole cells of Saccharomyces cerevisiae yeast.

  2. Shock Electrodeposition in Charged Porous Media

    CERN Document Server

    Han, Ji-Hyung

    2015-01-01

    It is shown that surface conduction in porous media can drastically alter the stability and morphology of electrodeposition at high rates, above the diffusion-limited current. Copper electrodeposits are visualized by scanning electron microscopy and energy dispersive spectroscopy in cellulose nitrate membranes, whose pores are coated with positive or negative charged polymers. Above the limiting current, surface conduction inhibits growth in the positive membrane and produces irregular dendrites, while it enhances growth and suppresses dendrites behind a deionization shock in the negative membrane. The discovery of uniform growth contradicts quasi-steady leaky membrane models, which are in the same universality class as unstable Laplacian growth, and indicates the importance of transient electro-diffusion or electro-osmotic dispersion. Shock electrodeposition could be exploited for high-rate recharging of metal batteries or manufacturing of metal matrix composite coatings.

  3. Porous Silicon Structures as Optical Gas Sensors

    Directory of Open Access Journals (Sweden)

    Igor A. Levitsky

    2015-08-01

    Full Text Available We present a short review of recent progress in the field of optical gas sensors based on porous silicon (PSi and PSi composites, which are separate from PSi optochemical and biological sensors for a liquid medium. Different periodical and nonperiodical PSi photonic structures (bares, modified by functional groups or infiltrated with sensory polymers are described for gas sensing with an emphasis on the device specificity, sensitivity and stability to the environment. Special attention is paid to multiparametric sensing and sensor array platforms as effective trends for the improvement of analyte classification and quantification. Mechanisms of gas physical and chemical sorption inside PSi mesopores and pores of PSi functional composites are discussed.

  4. Porous polyoxadiazole membranes for harsh environment

    KAUST Repository

    Maab, Husnul

    2013-10-01

    A series of polyoxadiazoles with exceptionally high stability at temperatures as high as 370°C and in oxidative medium has been synthesized by polycondensation and manufactured into porous membranes by phase inversion. The membranes were characterized by thermal analysis (TGA), chemical stability was measured by immersion test, oxidative stability by Fenton\\'s test, pore diameter by porosimetry and the morphology by FESEM. The polymers are soluble only in sulfuric acid and are stable in organic solvents like NMP, THF and isopropanol. The membranes selectivity was confirmed by separation of polystyrene standards with different molecular weights. Most membranes were characterized as having a cut-off of 60,000. g/mol. Being stable under harsh environments, the membranes have incomparable characteristics with perspectives of application in chemical and pharmaceutical industry, catalytic reactors, in combination with oxidative processes and other applications so far envisioned only for ceramic membranes. © 2013.

  5. Statistics of linear polymers in disordered media

    CERN Document Server

    Chakrabarti, Bikas K

    2005-01-01

    With the mapping of the partition function graphs of the n-vector magnetic model in the n to 0 limit as the self-avoiding walks, the conformational statistics of linear polymers was clearly understood in early seventies. Various models of disordered solids, percolation model in particular, were also established by late seventies. Subsequently, investigations on thestatistics of linear polymers or of self-avoiding walks in, say, porous medium or disordered lattices were started in early eighties. Inspite of the brilliant ideas forwarded and extensive studies made for the next two decades, the

  6. Formation of porous networks on polymeric surfaces by femtosecond laser micromachining

    Science.gov (United States)

    Assaf, Youssef; Kietzig, Anne-Marie

    2017-02-01

    In this study, porous network structures were successfully created on various polymer surfaces by femtosecond laser micromachining. Six different polymers (poly(tetrafluoroethylene) (PTFE), poly(methyl methacrylate) (PMMA), high density poly(ethylene) (HDPE), poly(lactic acid) (PLA), poly(carbonate) (PC), and poly(ethylene terephthalate) (PET)) were machined at different fluences and pulse numbers, and the resulting structures were identified and compared by lacunarity analysis. At low fluence and pulse numbers, porous networks were confirmed to form on all materials except PLA. Furthermore, all networks except for PMMA were shown to bundle up at high fluence and pulse numbers. In the case of PC, a complete breakdown of the structure at such conditions was observed. Operation slightly above threshold fluence and at low pulse numbers is therefore recommended for porous network formation. Finally, the thickness over which these structures formed was measured and compared to two intrinsic material dependent parameters: the single pulse threshold fluence and the incubation coefficient. Results indicate that a lower threshold fluence at operating conditions favors material removal over structure formation and is hence detrimental to porous network formation. Favorable machining conditions and material-dependent parameters for the formation of porous networks on polymer surfaces have thus been identified.

  7. Porous media for catalytic renewable energy conversion

    Science.gov (United States)

    Hotz, Nico

    2012-05-01

    A novel flow-based method is presented to place catalytic nanoparticles into a reactor by sol-gelation of a porous ceramic consisting of copper-based nanoparticles, silica sand, ceramic binder, and a gelation agent. This method allows for the placement of a liquid precursor containing the catalyst into the final reactor geometry without the need of impregnating or coating of a substrate with the catalytic material. The so generated foam-like porous ceramic shows properties highly appropriate for use as catalytic reactor material, e.g., reasonable pressure drop due to its porosity, high thermal and catalytic stability, and excellent catalytic behavior. The catalytic activity of micro-reactors containing this foam-like ceramic is tested in terms of their ability to convert alcoholic biofuel (e.g. methanol) to a hydrogen-rich gas mixture with low concentrations of carbon monoxide (up to 75% hydrogen content and less than 0.2% CO, for the case of methanol). This gas mixture is subsequently used in a low-temperature fuel cell, converting the hydrogen directly to electricity. A low concentration of CO is crucial to avoid poisoning of the fuel cell catalyst. Since conventional Polymer Electrolyte Membrane (PEM) fuel cells require CO concentrations far below 100 ppm and since most methods to reduce the mole fraction of CO (such as Preferential Oxidation or PROX) have CO conversions of up to 99%, the alcohol fuel reformer has to achieve initial CO mole fractions significantly below 1%. The catalyst and the porous ceramic reactor of the present study can successfully fulfill this requirement.

  8. Polymer-Enhanced Subsurface Delivery and Distribution of Permanganate

    Science.gov (United States)

    2013-02-01

    molecules can become trapped within narrow pores during transport with porous media, reducing the permeability to polymer and in severe cases to water...result of filtration and entrapment of these large polymer molecules within narrow pores and pore pathways. Transport experiments utilizing site aquifer...and the surrounding paved and grassy areas, located on Post Lane Road, approximately 500 feet east of the intersection of Post Lane Road and McHugh

  9. Guest-responsive reversible swelling and enhanced fluorescence in a super-absorbent, dynamic microporous polymer.

    Science.gov (United States)

    Rao, K Venkata; Mohapatra, Sudip; Maji, Tapas Kumar; George, Subi J

    2012-04-10

    A swell idea! The guest-responsive reversible swelling and fluorescence enhancement of a dynamic, microporous polymer network is presented. Guest-induced breathing of hydrophobic pores imparts multi-functional properties, such as super-absorbency, phase-selective swelling of oil from water and encapsulation of C(60) (see figure), to this soft micro-porous organic polymer.

  10. Organometallic Polymers.

    Science.gov (United States)

    Carraher, Charles E., Jr.

    1981-01-01

    Reactions utilized to incorporate a metal-containing moiety into a polymer chain (addition, condensation, and coordination) are considered, emphasizing that these reactions also apply to smaller molecules. (JN)

  11. Electrochemical Synthesis of a Microporous Conductive Polymer Based on a Metal-Organic Framework Thin Film

    KAUST Repository

    Lu, Chunjing

    2014-05-22

    A new approach to preparing 3D microporous conductive polymer has been demonstrated in the electrochemical synthesis of a porous polyaniline network with the utilization of a MOF thin film supported on a conducting substrate. The prepared porous polyaniline with well-defined uniform micropores of 0.84 nm exhibits a high BET surface area of 986 m2 g−1 and a high electric conductivity of 0.125 S cm−1 when doped with I2, which is superior to existing porous conducting materials of porous MOFs, CMPs, and COFs.

  12. Polymers All Around You!

    Science.gov (United States)

    Gertz, Susan

    Background information on natural polymers, synthetic polymers, and the properties of polymers is presented as an introduction to this curriculum guide. Details are provided on the use of polymer products in consumer goods, polymer recycling, polymer densities, the making of a polymer such as GLUEP, polyvinyl alcohol, dissolving plastics, polymers…

  13. Preparation and characterization of porous titania-grafted poly(styrene-divinylbenzene)/maleic anhydride nanocomposite microspheres

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Mesoporous titania-grafted poly(styrene-divinylbenzene)/maleic anhydride [P(St-DVB)/MA] nanocomposite microspheres were prepared by an open ring reaction method.The titania nanoparticles were first modified by attachment of amino groups to their surface to prevent particle aggregation,and to allow the nanoparticles to covalently bond the polymer microspheres,the surface of which was modified by attachment of MA functional groups to enable the polymer to retain their porous structures and to react with the amino groups on the surface of the titania particles.The porous nanocomposite microspheres were detected by FTIR,SEM,TEM,XRD and UV-Vis spectrophotometry.The results indicated that the nanocomposite microspheres were composed of nanosized titania uniformly distributed on the surface,and exhibited better UV absorbing property than pure polymer microspheres or unmodified titania.Furthermore,compared with pure porous polymer microspheres,the nanocomposite microspheres showed more efficient UV protection and slow release of Parsol-1789(a photo-reactive and cosmetic agent) held inside the porous network of the microspheres.

  14. Rapid Production of a Porous Cellulose Acetate Membrane for Water Filtration Using Readily Available Chemicals

    Science.gov (United States)

    Kaiser, Adrian; Stark, Wendelin J.; Grass, Robert N.

    2017-01-01

    A chemistry laboratory experiment using everyday items and readily available chemicals is described to introduce advanced high school students and undergraduate college students to porous polymer membranes. In a three-step manufacturing process, a membrane is produced at room temperature. The filtration principle of the membrane is then…

  15. Phase-inversion tape casting and synchrotron-radiation computed tomography analysis of porous alumina

    NARCIS (Netherlands)

    Fang, H.; Ren, C.; Liu, Yaoge; Lu, D.; Winnubst, A.J.A.; Chen, Chusheng

    2013-01-01

    A variant of tape casting based on the phase inversion phenomenon was adopted for fabrication of porous ceramic wafer. A slurry was prepared by dispersing alumina powder in an N-methyl-2-pyrrolidone (NMP) solution of the polymers polyethersulfone (PES) and polyvinylpyrrolidone (PVP). The slurry was

  16. Porous stainless steel hollow fibers with shrinkage-controlled small radial dimensions

    NARCIS (Netherlands)

    Luiten-Olieman, Mieke W.J.; Raaijmakers, Michiel J.T.; Winnubst, Louis; Wessling, Matthias; Nijmeijer, Arian; Benes, Nieck E.

    2011-01-01

    A method is presented for the preparation of thin (∼250 μm) porous stainless steel hollow fiber membranes based on dry–wet spinning of a particle-loaded polymer solution followed by heat treatment. Extraordinarily small radial dimensions were achieved by controlled shrinkage during thermal treatment

  17. Phase-inversion tape casting and synchrotron-radiation computed tomography analysis of porous alumina

    NARCIS (Netherlands)

    Fang, Hong; Ren, Chunlei; Liu, Yaoge; Lu, Detang; Winnubst, Aloysius J.A.; Chen, Chusheng

    2013-01-01

    A variant of tape casting based on the phase inversion phenomenon was adopted for fabrication of porous ceramic wafer. A slurry was prepared by dispersing alumina powder in an N-methyl-2-pyrrolidone (NMP) solution of the polymers polyethersulfone (PES) and polyvinylpyrrolidone (PVP). The slurry was

  18. Preparation of advanced porous structures by stereolithography for application in tissue engineering

    NARCIS (Netherlands)

    Melchels, Ferry Petrus Wilhelmus

    2010-01-01

    Stereolithography is a solid freeform fabrication technique, with which computer-designed objects can be automatically fabricated from photo-curable polymer resins in a layer-by-layer manner. In tissue engineering, there is a need for porous structures with well-defined external geometries and inte

  19. Preparation and characteristics of porous ceramics

    Institute of Scientific and Technical Information of China (English)

    Dongmei SHAO; Peiping ZHANG; Liyan MA; Juanjuan LIU

    2007-01-01

    Pyrophyllite is always used for making porous ceramics. In order to design the preparation technics of porous ceramics with pyrophyllite reasonably we must know the classifications, characteristics, properties and applications of porous ceramics. The classification and characteristics of porous ceramics are reviewed in this article; and several common preparations with their advantages and disadvantages are also introduced. The authors discussed the problems existing in researching and developing process for porous ceramics, and forecasted the development prospect of porous ceramics.

  20. Nanoporous polymers for hydrogen storage.

    Science.gov (United States)

    Germain, Jonathan; Fréchet, Jean M J; Svec, Frantisek

    2009-05-01

    The design of hydrogen storage materials is one of the principal challenges that must be met before the development of a hydrogen economy. While hydrogen has a large specific energy, its volumetric energy density is so low as to require development of materials that can store and release it when needed. While much of the research on hydrogen storage focuses on metal hydrides, these materials are currently limited by slow kinetics and energy inefficiency. Nanostructured materials with high surface areas are actively being developed as another option. These materials avoid some of the kinetic and thermodynamic drawbacks of metal hydrides and other reactive methods of storing hydrogen. In this work, progress towards hydrogen storage with nanoporous materials in general and porous organic polymers in particular is critically reviewed. Mechanisms of formation for crosslinked polymers, hypercrosslinked polymers, polymers of intrinsic microporosity, and covalent organic frameworks are discussed. Strategies for controlling hydrogen storage capacity and adsorption enthalpy via manipulation of surface area, pore size, and pore volume are discussed in detail.

  1. Light Emitting Porous Silicon

    Science.gov (United States)

    1993-05-01

    ml - mm m lm m ~ m m ThO report Page 14 preparation method which has been originally described by Wohler [23] leads to a bright yellow substance with...Solid State Commun. 81, 307 (1992). [221 H. Kautsky, and H. Zocher, Z. Phys. 9,267 (1992). L TNO report Page 28 [231 F. Wohler , Lieb. Ann. 127, 275 (1863...Netherlands Fax + 31 70 328 09 61 Phone + 31 70 326 42 21 TNO- report copy no. e FEL-93eo047r Lh Emitting Porous Silicon sitho(s): DTICHMi.P.Th

  2. Porous Thermoelectric Materials

    Directory of Open Access Journals (Sweden)

    Hiroshi Julian Goldsmid

    2009-08-01

    Full Text Available Thermoelectric materials are sometimes prepared using a sintering process in which the achievement of a high density is often one of the objectives. However, it has recently been shown that the introduction of a highly porous material is desirable in synthetic transverse thermoelements. Porosity may also be an advantage in conventional longitudinal thermoelectric modules in which a high thermal flux density creates problems, but heat transfer within the pores can degrade the thermoelectric figure of merit. The amount of this degradation is calculated and it is shown that it can be small enough to be acceptable in practical devices.

  3. Tortuosity of porous particles.

    Science.gov (United States)

    Barrande, M; Bouchet, R; Denoyel, R

    2007-12-01

    Tortuosity is often used as an adjustable parameter in models of transfer properties through porous media. This parameter, not reducible to classical measured microstructural parameters like specific surface area, porosity, or pore size distribution, reflects the efficiency of percolation paths, which is linked to the topology of the material. The measurement of the effective conductivity of a bed of particles saturated with an electrolyte is a simple way to evaluate tortuosity. Nevertheless, it received only little attention because of the real difficulties in both getting reliable results and interpreting data. Notably, the discrimination between the contribution of interparticle and intraparticle porosities to the tortuosity is not resolved. To our knowledge, there is no model able to fit the experimental data of the tortuosity of a suspension, and a fortiori of a particle bed, in the whole porosity range. Only empirical expressions have been proposed, but they do not allow deriving intratortuosity of a porous particle. For a dilute system, Maxwell's equation predicts the effective conductivity of suspensions of spherical particles as a function of the bulk electrolyte conductivity and of particle conductivity. The intraparticle tortuosity can be derived from the particle conductivity obtained from the Maxwell equation applied to data at infinite dilution of particles. Then, by assuming that the Maxwell equation is a first-order approximation of the conductivity as a function of porosity, we propose an explicit relation of the tortuosity tau of a suspension of porous particles, obtained by conductivity measurement, as tau = tau(epsilon, epsilon(p), tau(p)), where epsilon is the total porosity of the suspension, tau(p) is the intraparticle tortuosity, and epsilon(p) is the particle porosity. This relationship fits the experimental data in the whole porosity range and can be used to determine tau(p) from an experiment at only one porosity. Finally, the obtained

  4. Fullerene-doped porous glasses

    Science.gov (United States)

    Joshi, M. P.; Kukreja, L. M.; Rustagi, K. C.

    We report the doping of C60 in porous glass by diffusion in solution phase at room temperature. The presence of C60 in the doped porous glass was confirmed spectroscopically. We also report the changes in optical absorption spectrum and intensity-dependent transmission of 30 ns laser pulses at 527 nm in these materials.

  5. Fullerene-doped porous glasses

    Energy Technology Data Exchange (ETDEWEB)

    Joshi, M.P. [Center for Adv. Technol., Indore (India). Nonlinear Optics Group; Kukreja, L.M. [Center for Adv. Technol., Indore (India). Nonlinear Optics Group; Rustagi, K.C. [Center for Adv. Technol., Indore (India). Nonlinear Optics Group

    1997-07-01

    We report the doping of C{sub 60} in porous glass by diffusion in solution phase at room temperature. The presence of C{sub 60} in the doped porous glass was confirmed spectroscopically. We also report the changes in optical absorption spectrum and intensity-dependent transmission of 30 ns laser pulses at 527 nm in these materials. (orig.)

  6. Moisture Sorption in Porous Materials

    DEFF Research Database (Denmark)

    Nielsen, Lauge Fuglsang

    2007-01-01

    Abstract: Information on pore geometry is very important in any study of the mechanical and physical behavior of porous materials. Unfortunately pores are not very accessible for direct measurements. Indirect methods have to be used which involve impregnation (sorption) experiments from which...... in the subject considered this software is available on request to the author. Keywords: Porous materials, moisture, adsorption, desorption, BET-parameters....

  7. Aerosol dynamics in porous media

    NARCIS (Netherlands)

    Ghazaryan, Lilya

    2014-01-01

    In this thesis, a computational model was developed for the simulation of aerosol formation through nucleation, followed by condensation and evaporation and filtration by porous material. Understanding aerosol dynamics in porous media can help improving engineering models that are used in various in

  8. An Overview of Recent Development in Composite Catalysts from Porous Materials for Various Reactions and Processes

    Directory of Open Access Journals (Sweden)

    Zaiku Xie

    2010-05-01

    Full Text Available Catalysts are important to the chemical industry and environmental remediation due to their effective conversion of one chemical into another. Among them, composite catalysts have attracted continuous attention during the past decades. Nowadays, composite catalysts are being used more and more to meet the practical catalytic performance requirements in the chemical industry of high activity, high selectivity and good stability. In this paper, we reviewed our recent work on development of composite catalysts, mainly focusing on the composite catalysts obtained from porous materials such as zeolites, mesoporous materials, carbon nanotubes (CNT, etc. Six types of porous composite catalysts are discussed, including amorphous oxide modified zeolite composite catalysts, zeolite composites prepared by co-crystallization or overgrowth, hierarchical porous catalysts, host-guest porous composites, inorganic and organic mesoporous composite catalysts, and polymer/CNT composite catalysts.

  9. Solution electrospinning of particle-polymer composite fibres

    DEFF Research Database (Denmark)

    Christiansen, Lasse; Fojan, Peter

    2016-01-01

    into scaffolds. The formation of a particle/polymer composite results in improved mechanical stability, without compromising the porosity. In the presented study, aerogel and poly(ethylene oxide) are mixed into a solution, and spun to thin fibres. Thereby a porous membrane, on the micro- and nano...

  10. Sulfamides and sulfamide polymers directly from sulfur dioxide.

    Science.gov (United States)

    Leontiev, Alexander V; Dias, H V Rasika; Rudkevich, Dmitry M

    2006-07-21

    SO2 gas is effectively used for the preparation of N,N'-diarylsulfamides and shape-persistent sulfamide polymers, which utilize a network of intermolecular N-H...O=S hydrogen bonds to self-assemble into soft porous materials.

  11. PREPARATION OF CARBON NANOFIBERS BY POLYMER BLEND TECHNIQUE

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The polymer blend technique is a novel method to produced carbon nanofibers. In this paper, we have prepared fine carbon fibers and porous carbon materials by this technique, and we will discuss the experiment results by means of SEM, TGA, Element Analysis, etc.

  12. Electrospun a-Si using Liquid Silane/Polymer Inks

    Energy Technology Data Exchange (ETDEWEB)

    Doug Schulz

    2010-12-09

    Amorphous silicon nanowires (a-SiNWs) were prepared by electrospinning cyclohexasilane (Si{sub 6}H{sub 12}) admixed with polymethylmethacrylate (PMMA) in toluene. Raman spectroscopy characterization of these wires (d {approx} 50-2000 nm) shows 350 C treatment yields a-SiNWs. Porous a-SiNWs are obtained using a volatile polymer.

  13. Local mobility of polymer chain grafted onto polyethylene monitored by fluorescence depolarization

    Science.gov (United States)

    Tsuneda, Satoshi; Endo, Toshihiro; Saito, Kyoichi; Sugita, Kazuyuki; Horie, Kazuyuki; Yamashita, Takashi; Sugo, Takanobu

    1997-08-01

    The fluorescence depolarization method was used for investigating the local mobility of polymer chains grafted onto a porous polyethylene membrane. The real value of the rotational diffusion coefficient of a dansyl probe attached to the grafted polymer chain was obtained by using a correction method which eliminated the effect of multiple scattering on fluorescence anisotropy. The rotational mobility of the dansyl probe attached to the grafted polymer chain was sensitive to both degree of grafting and solvent polarity, which indicated that the conformation of the grafted polymer chain and the pore size of the base membrane strongly governed the dynamic parameters of the grafted polymer chain.

  14. Fabrication of Porous Materials from Natural/Synthetic Biopolymers and Their Composites

    Directory of Open Access Journals (Sweden)

    Udeni Gunathilake T.M. Sampath

    2016-12-01

    Full Text Available Biopolymers and their applications have been widely studied in recent years. Replacing the oil based polymer materials with biopolymers in a sustainable manner might give not only a competitive advantage but, in addition, they possess unique properties which cannot be emulated by conventional polymers. This review covers the fabrication of porous materials from natural biopolymers (cellulose, chitosan, collagen, synthetic biopolymers (poly(lactic acid, poly(lactic-co-glycolic acid and their composite materials. Properties of biopolymers strongly depend on the polymer structure and are of great importance when fabricating the polymer into intended applications. Biopolymers find a large spectrum of application in the medical field. Other fields such as packaging, technical, environmental, agricultural and food are also gaining importance. The introduction of porosity into a biomaterial broadens the scope of applications. There are many techniques used to fabricate porous polymers. Fabrication methods, including the basic and conventional techniques to the more recent ones, are reviewed. Advantages and limitations of each method are discussed in detail. Special emphasis is placed on the pore characteristics of biomaterials used for various applications. This review can aid in furthering our understanding of the fabrication methods and about controlling the porosity and microarchitecture of porous biopolymer materials.

  15. Fabrication of Porous Materials from Natural/Synthetic Biopolymers and Their Composites.

    Science.gov (United States)

    Sampath, Udeni Gunathilake T M; Ching, Yern Chee; Chuah, Cheng Hock; Sabariah, Johari J; Lin, Pai-Chen

    2016-12-07

    Biopolymers and their applications have been widely studied in recent years. Replacing the oil based polymer materials with biopolymers in a sustainable manner might give not only a competitive advantage but, in addition, they possess unique properties which cannot be emulated by conventional polymers. This review covers the fabrication of porous materials from natural biopolymers (cellulose, chitosan, collagen), synthetic biopolymers (poly(lactic acid), poly(lactic-co-glycolic acid)) and their composite materials. Properties of biopolymers strongly depend on the polymer structure and are of great importance when fabricating the polymer into intended applications. Biopolymers find a large spectrum of application in the medical field. Other fields such as packaging, technical, environmental, agricultural and food are also gaining importance. The introduction of porosity into a biomaterial broadens the scope of applications. There are many techniques used to fabricate porous polymers. Fabrication methods, including the basic and conventional techniques to the more recent ones, are reviewed. Advantages and limitations of each method are discussed in detail. Special emphasis is placed on the pore characteristics of biomaterials used for various applications. This review can aid in furthering our understanding of the fabrication methods and about controlling the porosity and microarchitecture of porous biopolymer materials.

  16. Characterization and Optimization of Polymer-Ceramic Pressure-Sensitive Paint by Controlling Polymer Content

    Directory of Open Access Journals (Sweden)

    Hitoshi Ishikawa

    2011-07-01

    Full Text Available A pressure-sensitive paint (PSP with fast response characteristics that can be sprayed on a test article is studied. This PSP consists of a polymer for spraying and a porous particle for providing the fast response. We controlled the polymer content (% from 10 to 90% to study its effects on PSP characteristics: the signal level, pressure sensitivity, temperature dependency, and time response. The signal level and temperature dependency shows a peak in the polymer content around 50 to 70%. The pressure sensitivity was fairly constant in the range between 0.8 and 0.9 %/kPa. The time response is improved by lowering the polymer content. The variation of the time response is shown to be on the order of milliseconds to ten seconds. A weight coefficient is introduced to optimize the resultant PSPs. By setting the weight coefficient, we can optimize the PSP for sensing purposes.

  17. Fabrication of Porous Scaffolds Using NaHCO3 Particulates as the Porogen Material

    Institute of Scientific and Technical Information of China (English)

    SHEN Xiongjun; RUAN Jianming; ZHOU Zhongcheng; ZHANG Haipo; ZHOU Zhihua

    2007-01-01

    A new method of fabricating porous polymer scaffolds was developed, using sodium hydrogen carbonate particulates as the porogen to foam. The pore structure of polymer scaffolds can easily be manipulated by controlling the size and weight fraction of sodium hydrogen carbonate particulates. The scaffolds are highly porous with a porosity greater than 90% and with a larger pore size ranging from 100-400 μm, and are well distributed with the interconnected and open pore wall structure which is necessary for tissue engineering. We investigated the effect of the porosity of scaffolds, the pore size of scaffolds and material of polymer on the mechanical properties of scaffolds. The scaffolds fabricated by the method have more big pores than those by the convenient method of salt leaching.

  18. Characterization of Elastic Properties of Porous Graphene Using an Ab Initio Study

    Directory of Open Access Journals (Sweden)

    Reza Ansari

    2016-12-01

    Full Text Available Importance of covalent bonded two-dimensional monolayer nanostructures and also hydrocarbons is undeniably responsible for creation of new fascinating materials like polyphenylene polymer, a hydrocarbon super honeycomb network, so-called porous graphene. The mechanical properties of porous graphene such as its Young’s modulus, Poisson’s ratio and the bulk modulus as the determinative properties are calculated in this paper using ab initio calculations. To accomplish this aim, the density functional theory on the basis of generalized gradient approximation and the Perdew–Burke–Ernzerhof exchange correlation is employed. Density functional theory calculations are used to calculate strain energy of porous graphene with respect to applied strain. Selected numerical results are then presented to study the properties of porous graphene. Comparisons are made between the properties of porous graphene and those of other analogous nanostructures. The results demonstrated lower stiffness of porous graphene than those of graphene and graphyne, and higher stiffness than that of graphdyine and other graphyne families. Unlikely, Poisson’s ratio is observed to be more than that of graphene and also less than that of graphyne. It is further observed that the presence of porosity and also formation of C-H bond in the pore sites is responsible for these discrepancies. Porous graphene is found to behave as the isotropic material.

  19. A study on improving mechanical properties of porous HA tissue engineering scaffolds by hot isostatic pressing

    Energy Technology Data Exchange (ETDEWEB)

    Zhao Jing [Key Laboratory of Advanced Technologies of Materials (Ministry of Education), School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Xiao Suguang [Key Laboratory of Advanced Technologies of Materials (Ministry of Education), School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Lu Xiong [Key Laboratory of Advanced Technologies of Materials (Ministry of Education), School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Wang Jianxin [Key Laboratory of Advanced Technologies of Materials (Ministry of Education), School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Weng Jie [Key Laboratory of Advanced Technologies of Materials (Ministry of Education), School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China)

    2006-12-15

    Various interconnected porous hydroxyapatite (HA) ceramic scaffolds are universally used to induct the tissue growth for bone repair and replacement, and serve to support the adhesion, transfer, proliferation and differentiation of cells. Impregnation of polyurethane sponges with a ceramic slurry is adopted to produce highly porous HA ceramic scaffolds with a 3D interconnected structure. However, high porosity always accompanies a decrease in the strength of the HA ceramic scaffolds. Therefore, it is significant to improve the strength of the HA ceramic scaffolds with highly interconnected porosity so that they are more suitable in clinical applications. In this work, highly porous HA ceramic scaffolds are first produced by the polymer impregnation approach, and subsequently further sintered by hot isostatic pressing (HIP). The phase composition, macro- and micro-porous structure, sintering and mechanical properties of the porous HA scaffolds are investigated by x-ray diffraction (XRD), scanning electron microscopy (SEM), nanoindentation analysis and compressive test. The experimental results show that the nanohardness and compressive strength of HIP-sintered porous HA ceramics are higher than those of commonly sintered HA scaffolds. The HIP technique can effectively improve the sintering property and densification of porous HA ceramic scaffolds, so inducing an increase in the compression strength.

  20. Porous poly(perfluorosulfonic acid) membranes for alkaline water electrolysis

    DEFF Research Database (Denmark)

    Aili, David; Hansen, Martin Kalmar; Andreasen, Jens Wenzel;

    2015-01-01

    and washed out and the obtained porous materials allowed for swelling to reach water contents up to λ=85 [H2O] [−SO3K]−1. After equilibration in 22 wt% aqueous KOH, ion conductivity of 0.2 S cm−1 was recorded for this membrane type at room temperature, which is significantly higher than 0.01 S cm−1......Poly(perfluorosulfonic acid) (PFSA) is one of a few polymer types that combine excellent alkali resistance with extreme hydrophilicity. It is therefore of interest as a base material in separators for alkaline water electrolyzers. In the pristine form it, however, shows high cation selectivity....... To increase its ion conductivity in aqueous KOH, a method for the preparation of porous PFSA membranes was developed. It was based on an approach where PFSA was co-cast with poly(vinylpyrrolidone) (PVP) at different ratios to give transparent and colorless blend membranes. The PVP was subsequently dissolved...

  1. Preparation of porous carbon particle with shell/core structure

    Directory of Open Access Journals (Sweden)

    2007-05-01

    Full Text Available Porous carbon particles with a shell/core structure have been prepared successfully by controlled precipitation of the polymer from droplets of oil-in-water emulsion, followed by curing and carbonization. The droplets of the oil phase are composed of phenolic resin (PFR, a good solvent (ethyl acetate and porogen (Poly(methyl methacrylate, PMMA. The microstructure was characterized in detail by scanning electron microscopy (SEM, transmission electron microscopy (TEM, nitrogen adsorption, and thermo gravimetric analysis (TGA. The obtained carbon particles have a capsular structure with a microporous carbon shell and a mesoporous carbon core. The BET surface area and porous volume are calculated to be 499 m2g-1 and 0.56 cm3g-1, respectively. The effects of the amount of porogen (PMMA, co-solvent (acetone and surfactant on the resultant structure were studied in detail.

  2. Piezoelectrets from sandwiched porous polytetrafluoroethylene (ePTFE) films: influence of porosity and geometry on charging properties

    Energy Technology Data Exchange (ETDEWEB)

    Zhukov, Sergey; Von Seggern, Heinz [Institute of Materials Science, Technische Universitaet Darmstadt, Petersenstrasse 23, 64287 Darmstadt (Germany); Fedosov, Sergey, E-mail: zhukov@e-mat.tu-darmstadt.de [Department of Physics and Materials Science, Odessa National Academy of Food Technologies, Kanatnaya 112, 65039 Odessa (Ukraine)

    2011-03-16

    Sandwiched structures of open-porous and solid polymer dielectrics reveal a strong piezoelectric response after proper charging by high electric fields. Here, the electrical properties of corona-poled three-layer FEP/ePTFE/FEP sandwiches are studied theoretically and experimentally with the objective of its possible optimization for the highest piezoelectric activity. Modelling of the charging properties is performed for different sandwich geometries. It is shown that the maximum value of the remanent interface charge density accumulated during poling depends mainly on the ratio of the solid and porous layers thicknesses and on parameter E{sub B}, which characterizes the electric breakdown strength of air in the porous layer. E{sub B} exhibits specific dependences on porosity and thickness of the porous layer. For a given porous layer E{sub B} is independent of the solid film thickness. The obtained results can be utilized to further optimize the sandwich structure as an electromechanically active device.

  3. Antimocrobial Polymer

    Energy Technology Data Exchange (ETDEWEB)

    McDonald, William F. (Utica, OH); Huang, Zhi-Heng (Walnut Creek, CA); Wright, Stacy C. (Columbus, GA)

    2005-09-06

    A polymeric composition having antimicrobial properties and a process for rendering the surface of a substrate antimicrobial are disclosed. The composition comprises a crosslinked chemical combination of (i) a polymer having amino group-containing side chains along a backbone forming the polymer, (ii) an antimicrobial agent selected from quaternary ammonium compounds, gentian violet compounds, substituted or unsubstituted phenols, biguanide compounds, iodine compounds, and mixtures thereof, and (iii) a crosslinking agent containing functional groups capable of reacting with the amino groups. In one embodiment, the polymer is a polyamide formed from a maleic anhydride or maleic acid ester monomer and alkylamines thereby producing a polyamide having amino substituted alkyl chains on one side of the polyamide backbone; the crosslinking agent is a phosphine having the general formula (A)3P wherein A is hydroxyalkyl; and the antimicrobial agent is chlorhexidine, dimethylchlorophenol, cetyl pyridinium chloride, gentian violet, triclosan, thymol, iodine, and mixtures thereof.

  4. Polymer inflation

    CERN Document Server

    Hassan, Syed Moeez; Seahra, Sanjeev S

    2014-01-01

    We consider the semi-classical dynamics of a free massive scalar field in a homogeneous and isotropic cosmological spacetime. The scalar field is quantized using the polymer quantization method assuming that it is described by a gaussian coherent state. For quadratic potentials, the semi-classical equations of motion yield a universe that has an early "polymer inflation" phase which is generic and almost exactly de Sitter, followed by a epoch of slow-roll inflation. We compute polymer corrections to the slow roll formalism, and discuss the probability of inflation in this model using a physical Hamiltonian arising from time gauge fixing. These results show the extent to which a quantum gravity motivated quantization method affects early universe dynamics.

  5. Actuator device utilizing a conductive polymer gel

    Science.gov (United States)

    Chinn, Douglas A.; Irvin, David J.

    2004-02-03

    A valve actuator based on a conductive polymer gel is disclosed. A nonconductive housing is provided having two separate chambers separated by a porous frit. The conductive polymer is held in one chamber and an electrolyte solution, used as a source of charged ions, is held in the second chamber. The ends of the housing a sealed with a flexible elastomer. The polymer gel is further provide with electrodes with which to apply an electrical potential across the gel in order to initiate an oxidation reaction which in turn drives anions across the porous frit and into the polymer gel, swelling the volume of the gel and simultaneously contracting the volume of the electrolyte solution. Because the two end chambers are sealed the flexible elastomer expands or contracts with the chamber volume change. By manipulating the potential across the gel the motion of the elastomer can be controlled to act as a "gate" to open or close a fluid channel and thereby control flow through that channel.

  6. Polymer electronics

    CERN Document Server

    Geoghegan, Mark

    2013-01-01

    Polymer electronics is the science behind many important new developments in technology, such as the flexible electronic display (e-ink) and many new developments in transistor technology. Solar cells, light-emitting diodes, and transistors are all areas where plastic electronics is likely to, or is already having, a serious impact on our daily lives. With polymer transistors and light-emitting diodes now being commercialised, there is a clear need for a pedagogic text thatdiscusses the subject in a clear and concise fashion suitable for senior undergraduate and graduate students. The content

  7. Ceramic-in-polymer versus polymer-in-ceramic polymeric electrolytes - A novel approach

    Energy Technology Data Exchange (ETDEWEB)

    Syzdek, Jaroslaw [Warsaw University of Technology, Faculty of Chemistry, ul. Noakowskiego 3, 00-664 Warszawa (Poland); Universite de Picardie Jules Verne, Laboratoire de Reactivite et de Chimie des Solides, 33 Rue Saint-Leu, F-80039 Amiens Cedex (France); Armand, Michel [Universite de Picardie Jules Verne, Laboratoire de Reactivite et de Chimie des Solides, 33 Rue Saint-Leu, F-80039 Amiens Cedex (France); Gizowska, Magdalena; Marcinek, Marek; Sasim, Elzbieta; Szafran, Mikolaj; Wieczorek, Wladyslaw [Warsaw University of Technology, Faculty of Chemistry, ul. Noakowskiego 3, 00-664 Warszawa (Poland)

    2009-10-20

    A new type of composites, i.e. polymer-in-ceramic (as opposed to the ''classical'' ceramic-in-polymer approach) was introduced into the field of composite polymeric electrolytes. In this work the preparation of porous ceramic samples based on alumina is designed and their properties are characterised by XRD, porosimetry and SEM. Special setup was developed for the preparation of electrolytes in vacuum/controlled atmosphere conditions and it was used for preparing the composites. The studied systems exhibited excellent mechanical properties, high conductivities and good stability vs. Li metal electrodes under prolonged storage. (author)

  8. Multiphase flow in porous media using CFD

    DEFF Research Database (Denmark)

    Hemmingsen, Casper Schytte; Walther, Jens Honore

    We present results from a new Navier-Stokes model for multiphase flow in porous media implemented in Ansys Fluent 16.2 [1]. The model includes the Darcy-Forchheimer source terms in the momentum equations and proper account for relative permeability and capillary pressure in the porous media...... to model both the non-porous and porous media using the same formulation....

  9. Optimized manufacturable porous materials

    DEFF Research Database (Denmark)

    Andreassen, Erik; Andreasen, Casper Schousboe; Jensen, Jakob Søndergaard

    Topology optimization has been used to design two-dimensional material structures with specific elastic properties, but optimized designs of three-dimensional material structures are more scarsely seen. Partly because it requires more computational power, and partly because it is a major challenge...... to include manufacturing constraints in the optimization. This work focuses on incorporating the manufacturability into the optimization procedure, allowing the resulting material structure to be manufactured directly using rapid manufacturing techniques, such as selective laser melting/sintering (SLM....../S). The available manufacturing methods are best suited for porous materials (one constituent and void), but the optimization procedure can easily include more constituents. The elasticity tensor is found from one unit cell using the homogenization method together with a standard finite element (FE) discretization...

  10. Superhydrophobic Porous Silicon Surfaces

    Directory of Open Access Journals (Sweden)

    Paolo NENZI

    2011-12-01

    Full Text Available In this paper, we present an inexpensive technique to produce superhydrophobic surfaces from porous silicon. Superhydrophobic surfaces are a key technology for their ability to reduce friction losses in microchannels and their self cleaning properties. The morphology of a p-type silicon wafer is modified by a electrochemical wet etch to produce pores with controlled size and distribution and coated with a silane hydrophobic layer. Surface morphology is characterized by means of scanning electron microscope images. Large contact angles are observed on such surfaces and the results are compared with classical wetting models (Cassie and Wenzel suggesting a mixed Wenzel-Cassie behavior. The presented technique represents a cost-effective means for friction reduction in microfluidic applications, such as lab-on-a-chip.

  11. Filtration in Porous Media

    DEFF Research Database (Denmark)

    Yuan, Hao; Shapiro, Alexander

    There is a considerable and ongoing effort aimed at understanding the transport and the deposition of suspended particles in porous media, especially non-Fickian transport and non-exponential deposition of particles. In this work, the influential parameters in filtration models are studied...... to understand their effects on the non-Fickian transport and the non-exponential deposition. The filtration models are validated by the comparisons between the modelling results and the experimental data.The elliptic equation with distributed filtration coefficients may be applied to model non-Fickian transport...... and hyperexponential deposition. The filtration model accounting for the migration of surface associated particles may be applied for non-monotonic deposition....

  12. Convection in porous media

    CERN Document Server

    Nield, Donald A

    1992-01-01

    This book provides a user-friendly introduction to the topic of convection in porous media The authors as- sume that the reader is familiar with the basic elements of fluid mechanics and heat transfer, but otherwise the book is self-contained The book will be useful both as a review (for reference) and as a tutorial work, suitable as a textbook in a graduate course or seminar The book brings into perspective the voluminous research that has been performed during the last two decades The field has recently exploded because of worldwide concern with issues such as energy self-sufficiency and pollution of the environment Areas of application include the insulation of buildings and equipment, energy storage and recovery, geothermal reservoirs, nuclear waste disposal, chemical reactor engineering, and the storage of heat-generating materials such as grain and coal Geophysical applications range from the flow of groundwater around hot intrusions to the stability of snow against avalanches

  13. Porous media geometry and transports

    CERN Document Server

    Adler, Pierre

    1992-01-01

    The goal of ""Porous Media: Geometry and Transports"" is to provide the basis of a rational and modern approach to porous media. This book emphasizes several geometrical structures (spatially periodic, fractal, and random to reconstructed) and the three major single-phase transports (diffusion, convection, and Taylor dispersion).""Porous Media"" serves various purposes. For students it introduces basic information on structure and transports. Engineers will find this book useful as a readily accessible assemblage of al the major experimental results pertaining to single-phase tr

  14. Regeneratively Cooled Porous Media Jacket

    Science.gov (United States)

    Mungas, Greg (Inventor); Fisher, David J. (Inventor); London, Adam Pollok (Inventor); Fryer, Jack Merrill (Inventor)

    2013-01-01

    The fluid and heat transfer theory for regenerative cooling of a rocket combustion chamber with a porous media coolant jacket is presented. This model is used to design a regeneratively cooled rocket or other high temperature engine cooling jacket. Cooling jackets comprising impermeable inner and outer walls, and porous media channels are disclosed. Also disclosed are porous media coolant jackets with additional structures designed to transfer heat directly from the inner wall to the outer wall, and structures designed to direct movement of the coolant fluid from the inner wall to the outer wall. Methods of making such jackets are also disclosed.

  15. Properties of polymer - and fibre-modified porous asphalt mixes

    CSIR Research Space (South Africa)

    Verhaeghe, Benoit MJA

    1994-10-01

    Full Text Available In view of the increasing traffic volumes in South Africa and especially with regard to the impact of that on noise pollution and wet-weather accident rates in urban areas, the Southern African Bitumen and Tar Association expressed a need...

  16. Electroactive polymer based porous membranes for energy storage applications

    OpenAIRE

    Costa, Carlos Miguel da Silva

    2014-01-01

    Tese de doutoramento em Ciências (ramo de conhecimento em Física) In the field of mobile applications the efficient storage of energy is one of the most critical issues. Lithium ion batteries are lighter, cheaper, show higher energy density (210Wh kg-1), no memory effect, longer service-life and higher number of charge/discharge cycles than other battery solutions. The separator membrane is placed between the anode and cathode and serves as the medium for the transfer of charge, being a c...

  17. Molecularly Imprinted Polymers and Highly Porous Materials in Sensing Applications

    Science.gov (United States)

    2007-04-01

    microspheres from dilute dispersion polymerization systems (52). MIPs have also been prepared as imprinted membranes by precipitation of linear...and 1200m2/g. Supercritical drying of polysilsesquioxanes results in the formation of aerogels . These very low density materials have been

  18. Additive manufacturing of polymer-derived ceramics

    Science.gov (United States)

    Eckel, Zak C.; Zhou, Chaoyin; Martin, John H.; Jacobsen, Alan J.; Carter, William B.; Schaedler, Tobias A.

    2016-01-01

    The extremely high melting point of many ceramics adds challenges to additive manufacturing as compared with metals and polymers. Because ceramics cannot be cast or machined easily, three-dimensional (3D) printing enables a big leap in geometrical flexibility. We report preceramic monomers that are cured with ultraviolet light in a stereolithography 3D printer or through a patterned mask, forming 3D polymer structures that can have complex shape and cellular architecture. These polymer structures can be pyrolyzed to a ceramic with uniform shrinkage and virtually no porosity. Silicon oxycarbide microlattice and honeycomb cellular materials fabricated with this approach exhibit higher strength than ceramic foams of similar density. Additive manufacturing of such materials is of interest for propulsion components, thermal protection systems, porous burners, microelectromechanical systems, and electronic device packaging.

  19. Additive manufacturing of polymer-derived ceramics.

    Science.gov (United States)

    Eckel, Zak C; Zhou, Chaoyin; Martin, John H; Jacobsen, Alan J; Carter, William B; Schaedler, Tobias A

    2016-01-01

    The extremely high melting point of many ceramics adds challenges to additive manufacturing as compared with metals and polymers. Because ceramics cannot be cast or machined easily, three-dimensional (3D) printing enables a big leap in geometrical flexibility. We report preceramic monomers that are cured with ultraviolet light in a stereolithography 3D printer or through a patterned mask, forming 3D polymer structures that can have complex shape and cellular architecture. These polymer structures can be pyrolyzed to a ceramic with uniform shrinkage and virtually no porosity. Silicon oxycarbide microlattice and honeycomb cellular materials fabricated with this approach exhibit higher strength than ceramic foams of similar density. Additive manufacturing of such materials is of interest for propulsion components, thermal protection systems, porous burners, microelectromechanical systems, and electronic device packaging.

  20. Antimicrobial polymers.

    Science.gov (United States)

    Jain, Anjali; Duvvuri, L Sailaja; Farah, Shady; Beyth, Nurit; Domb, Abraham J; Khan, Wahid

    2014-12-01

    Better health is basic requirement of human being, but the rapid growth of harmful pathogens and their serious health effects pose a significant challenge to modern science. Infections by pathogenic microorganisms are of great concern in many fields such as medical devices, drugs, hospital surfaces/furniture, dental restoration, surgery equipment, health care products, and hygienic applications (e.g., water purification systems, textiles, food packaging and storage, major or domestic appliances etc.) Antimicrobial polymers are the materials having the capability to kill/inhibit the growth of microbes on their surface or surrounding environment. Recently, they gained considerable interest for both academic research and industry and were found to be better than their small molecular counterparts in terms of enhanced efficacy, reduced toxicity, minimized environmental problems, resistance, and prolonged lifetime. Hence, efforts have focused on the development of antimicrobial polymers with all desired characters for optimum activity. In this Review, an overview of different antimicrobial polymers, their mechanism of action, factors affecting antimicrobial activity, and application in various fields are given. Recent advances and the current clinical status of these polymers are also discussed.

  1. Polymer physics

    CERN Document Server

    Gedde, Ulf W

    1999-01-01

    This book is the result of my teaching efforts during the last ten years at the Royal Institute of Technology. The purpose is to present the subject of polymer physics for undergraduate and graduate students, to focus the fundamental aspects of the subject and to show the link between experiments and theory. The intention is not to present a compilation of the currently available literature on the subject. Very few reference citations have thus been made. Each chapter has essentially the same structure: starling with an introduction, continuing with the actual subject, summarizing the chapter in 30D-500 words, and finally presenting problems and a list of relevant references for the reader. The solutions to the problems presented in Chapters 1-12 are given in Chapter 13. The theme of the book is essentially polymer science, with the exclusion of that part dealing directly with chemical reactions. The fundamentals in polymer science, including some basic polymer chemistry, are presented as an introduction in t...

  2. Polymer/Carbon-Based Hybrid Aerogels: Preparation, Properties and Applications

    Directory of Open Access Journals (Sweden)

    Lizeng Zuo

    2015-10-01

    Full Text Available Aerogels are synthetic porous materials derived from sol-gel materials in which the liquid component has been replaced with gas to leave intact solid nanostructures without pore collapse. Recently, aerogels based on natural or synthetic polymers, called polymer or organic aerogels, have been widely explored due to their porous structures and unique properties, such as high specific surface area, low density, low thermal conductivity and dielectric constant. This paper gives a comprehensive review about the most recent progresses in preparation, structures and properties of polymer and their derived carbon-based aerogels, as well as their potential applications in various fields including energy storage, adsorption, thermal insulation and flame retardancy. To facilitate further research and development, the technical challenges are discussed, and several future research directions are also suggested in this review.

  3. Polymer-Coated Graphene Aerogel Beads and Supercapacitor Application.

    Science.gov (United States)

    Ouyang, An; Cao, Anyuan; Hu, Song; Li, Yanhui; Xu, Ruiqiao; Wei, Jinquan; Zhu, Hongwei; Wu, Dehai

    2016-05-01

    Graphene aerogels are highly porous materials with many energy and environmental applications; tailoring the structure and composition of pore walls within the aerogel is the key to those applications. Here, by freeze casting the graphene oxide sheets, we directly fabricated freestanding porous graphene beads containing radially oriented through channels from the sphere center to its surface. Furthermore, we introduced pseudopolymer to make reinforced, functional composite beads with a unique pore morphology. We showed that polymer layers can be coated smoothly on both sides of the pore walls, as well as on the junctions between adjacent pores, resulting in uniform polymer-graphene-polymer sandwiched structures (skeletons) throughout the bead. These composite beads significantly improved the electrochemical properties, with specific capacitances up to 669 F/g and good cyclic stability. Our results indicate that controlled fabrication of homogeneous hierarchical structures is a potential route toward high performance composite electrodes for various energy applications.

  4. The analysis of thermoplastic characteristics of special polymer sulfur composite

    Science.gov (United States)

    Książek, Mariusz

    2017-01-01

    Specific chemical environments step out in the industry objects. Portland cement composites (concrete and mortar) were impregnated by using the special polymerized sulfur and technical soot as a filler (polymer sulfur composite). Sulfur and technical soot was applied as the industrial waste. Portland cement composites were made of the same aggregate, cement and water. The process of special polymer sulfur composite applied as the industrial waste is a thermal treatment process in the temperature of about 150-155°C. The result of such treatment is special polymer sulfur composite in a liquid state. This paper presents the plastic constants and coefficients of thermal expansion of special polymer sulfur composites, with isotropic porous matrix, reinforced by disoriented ellipsoidal inclusions with orthotropic symmetry of the thermoplastic properties. The investigations are based on the stochastic differential equations of solid mechanics. A model and algorithm for calculating the effective characteristics of special polymer sulfur composites are suggested. The effective thermoplastic characteristics of special polymer sulfur composites, with disoriented ellipsoidal inclusions, are calculated in two stages: First, the properties of materials with oriented inclusions are determined, and then effective constants of a composite with disoriented inclusions are determined on the basis of the Voigt or Rice scheme. A brief summary of new products related to special polymer sulfur composites is given as follows: Impregnation, repair, overlays and precast polymer concrete will be presented. Special polymer sulfur as polymer coating impregnation, which has received little attention in recent years, currently has some very interesting applications.

  5. The analysis of thermoplastic characteristics of special polymer sulfur composite

    Science.gov (United States)

    Książek, Mariusz

    2016-07-01

    Specific chemical environments step out in the industry objects. Portland cement composites (concrete and mortar) were impregnated by using the special polymerized sulfur and technical soot as a filler (polymer sulfur composite). Sulfur and technical soot was applied as the industrial waste. Portland cement composites were made of the same aggregate, cement and water. The process of special polymer sulfur composite applied as the industrial waste is a thermal treatment process in the temperature of about 150-155°C. The result of such treatment is special polymer sulfur composite in a liquid state. This paper presents the plastic constants and coefficients of thermal expansion of special polymer sulfur composites, with isotropic porous matrix, reinforced by disoriented ellipsoidal inclusions with orthotropic symmetry of the thermoplastic properties. The investigations are based on the stochastic differential equations of solid mechanics. A model and algorithm for calculating the effective characteristics of special polymer sulfur composites are suggested. The effective thermoplastic characteristics of special polymer sulfur composites, with disoriented ellipsoidal inclusions, are calculated in two stages: First, the properties of materials with oriented inclusions are determined, and then effective constants of a composite with disoriented inclusions are determined on the basis of the Voigt or Rice scheme. A brief summary of new products related to special polymer sulfur composites is given as follows: Impregnation, repair, overlays and precast polymer concrete will be presented. Special polymer sulfur as polymer coating impregnation, which has received little attention in recent years, currently has some very interesting applications.

  6. A novel strategy for the preparation of porous microspheres and its application in peptide drug loading.

    Science.gov (United States)

    Wei, Yi; Wang, Yuxia; Zhang, Huixia; Zhou, Weiqing; Ma, Guanghui

    2016-09-15

    A new strategy is developed to prepare porous microspheres with narrow size distribution for peptides controlled release, involving a fabrication of porous microspheres without any porogens followed by a pore closing process. Amphiphilic polymers with different hydrophobic segments (poly(monomethoxypolyethylene glycol-co-d,l-lactide) (mPEG-PLA), poly(monomethoxypolyethylene glycol-co-d,l-lactic-co-glycolic acid) (mPEG-PLGA)) are employed as microspheres matrix to prepare porous microspheres based on a double emulsion-premix membrane emulsification technique combined with a solvent evaporation method. Both microspheres possess narrow size distribution and porous surface, which are mainly caused by (a) hydrophilic polyethylene glycol (PEG) segments absorbing water molecules followed by a water evaporation process and (b) local explosion of microspheres due to fast evaporation of dichloromethane (MC). Importantly, mPEG-PLGA microspheres have a honeycomb like structure while mPEG-PLA microspheres have a solid structure internally, illustrating that the different hydrophobic segments could modulate the affinity between solvent and matrix polymer and influence the phase separation rate of microspheres matrix. Long term release patterns are demonstrated with pore-closed microspheres, which are prepared from mPEG-PLGA microspheres loading salmon calcitonin (SCT). These results suggest that it is potential to construct porous microspheres for drug sustained release using permanent geometric templates as new porogens.

  7. Gelatin functionalised porous titanium alloy implants for orthopaedic applications

    Energy Technology Data Exchange (ETDEWEB)

    Vanderleyden, E. [Polymer Chemistry and Biomaterials Research Group, Department of Organic Chemistry, University of Ghent, Krijgslaan 281 S4, 9000 Ghent (Belgium); Van Bael, S. [Prometheus, Division of Skeletal Tissue Engineering, Katholieke Universiteit Leuven, O and N 1, Herestraat 49, Box 813, 3000 Leuven (Belgium); Department of Mechanical Engineering, Division of Production Engineering, Machine Design and Automation, Katholieke Universiteit Leuven, Celestijnenlaan 300b, 3001 Leuven (Belgium); Department of Mechanical Engineering, Division of Biomechanics and Engineering Design, Katholieke Universiteit Leuven, Celestijnenlaan 300c, Box 2419, 3001 Heverlee (Belgium); Chai, Y.C. [Prometheus, Division of Skeletal Tissue Engineering, Katholieke Universiteit Leuven, O and N 1, Herestraat 49, Box 813, 3000 Leuven (Belgium); Tissue Engineering Laboratory, Skeletal Biology and Engineering Research Center, Katholieke Universiteit Leuven, O and N 1, Herestraat 49, Box 813, 3000 Leuven (Belgium); Kruth, J.-P. [Department of Mechanical Engineering, Division of Production Engineering, Machine Design and Automation, Katholieke Universiteit Leuven, Celestijnenlaan 300b, 3001 Leuven (Belgium); Schrooten, J. [Prometheus, Division of Skeletal Tissue Engineering, Katholieke Universiteit Leuven, O and N 1, Herestraat 49, Box 813, 3000 Leuven (Belgium); Department of Metallurgy and Materials Engineering, Katholieke Universiteit Leuven, Kasteelpark Arenberg 44, Bus 2450, 3001 Leuven (Belgium); Dubruel, P., E-mail: pbmugent@gmail.com [Polymer Chemistry and Biomaterials Research Group, Department of Organic Chemistry, University of Ghent, Krijgslaan 281 S4, 9000 Ghent (Belgium)

    2014-09-01

    In the present work, we studied the immobilisation of the biopolymer gelatin onto the surface of three dimensional (3D) regular Ti6Al4V porous implants to improve their surface bio-activity. The successful immobilisation of the gelatin coating was made possible by a polydopamine interlayer, a polymer coating inspired by the adhesive nature of mussels. The presence of both coatings was first optimised on two dimensional titanium (2D Ti) substrates and confirmed by different techniques including X-ray photelectron spectroscopy, contact angle measurements, atomic force microscopy and fluorescence microscopy. Results showed homogeneous coatings that are stable for at least 24 h in phosphate buffer at 37 °C. In a next step, the coating procedure was successfully transferred to 3D Ti6Al4V porous implants, which indicates the versatility of the applied coating procedure with regard to complex surface morphologies. Furthermore, the bio-activity of these stable gelatin coatings was enhanced by applying a third and final coating using the cell-attractive protein fibronectin. The reproducible immobilisation process allowed for a controlled biomolecule presentation to the surrounding tissue. This newly developed coating procedure outperformed the previously reported silanisation procedure for immobilising gelatin. In vitro cell adhesion and culture studies with human periosteum-derived cells showed that the investigated coatings did not compromise the biocompatible nature of Ti6Al4V porous implants, but no distinct biological differences between the coatings were found. - Highlights: • Ti6Al4V porous implants were produced by selective laser melting. • A procedure to obtain a stable gelatin coating was developed. • Successful transfer of the coating procedure from 2D to 3D Ti6Al4V porous implants. • In vitro cell studies showed that the developed coatings supported cell growth.

  8. Transport phenomena in porous media

    CERN Document Server

    Ingham, Derek B

    1998-01-01

    Research into thermal convection in porous media has substantially increased during recent years due to its numerous practical applications. These problems have attracted the attention of industrialists, engineers and scientists from many very diversified disciplines, such as applied mathematics, chemical, civil, environmental, mechanical and nuclear engineering, geothermal physics and food science. Thus, there is a wealth of information now available on convective processes in porous media and it is therefore appropriate and timely to undertake a new critical evaluation of this contemporary information. Transport Phenomena in Porous Media contains 17 chapters and represents the collective work of 27 of the world's leading experts, from 12 countries, in heat transfer in porous media. The recent intensive research in this area has substantially raised the expectations for numerous new practical applications and this makes the book a most timely addition to the existing literature. It includes recent major deve...

  9. Porous substrates filled with nanomaterials

    Science.gov (United States)

    Worsley, Marcus A.; Baumann, Theodore F.; Satcher, Jr., Joe H.; Stadermann, Michael

    2014-08-19

    A composition comprising: at least one porous carbon monolith, such as a carbon aerogel, comprising internal pores, and at least one nanomaterial, such as carbon nanotubes, disposed uniformly throughout the internal pores. The nanomaterial can be disposed in the middle of the monolith. In addition, a method for making a monolithic solid with both high surface area and good bulk electrical conductivity is provided. A porous substrate having a thickness of 100 microns or more and comprising macropores throughout its thickness is prepared. At least one catalyst is deposited inside the porous substrate. Subsequently, chemical vapor deposition is used to uniformly deposit a nanomaterial in the macropores throughout the thickness of the porous substrate. Applications include electrical energy storage, such as batteries and capacitors, and hydrogen storage.

  10. Diffusion in porous crystalline materials

    NARCIS (Netherlands)

    Krishna, R.

    2012-01-01

    The design and development of many separation and catalytic process technologies require a proper quantitative description of diffusion of mixtures of guest molecules within porous crystalline materials. This tutorial review presents a unified, phenomenological description of diffusion inside meso-

  11. Porosity of porous Al alloys

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Two porosity models of porous Al alloys with different pore types (ball and polygon shape) were established. The experimental results coincide well with theoretical computations. The porosity of Al alloys (Prc) consists of three parts, porosity caused by preform particles (Prp), additional porosity (Pra), and porosity caused by solidification shrinkage (Prs). Prp is the main part of Prc while Pra is the key for fabricating porous Al alloys successfully in spite of its little contribution to Prc.

  12. A Green Method for Processing Polymers using Dense Gas Technology

    Directory of Open Access Journals (Sweden)

    Roshan B. Yoganathan

    2010-05-01

    Full Text Available Dense CO2 can be used as an environmentally-benign polymer processing medium because of its liquid-like densities and gas-like mass transfer properties.In this work, polymer bio-blends of polycarbonate (PC, a biocompatible polymer, and polycaprolactone (PCL, a biodegradable polymer were prepared. Dense CO2 was used as a reaction medium for the melt-phase PC polymerization in the presence of dense CO2-swollen PCL particles and this method was used to prepare porous PC/PCL blends. To extend the applicability of dense CO2 to the biomedical industry and polymer blend processing, the impregnation of ibuprofen into the blend was conducted and subsequent dissolution characteristics were observed.

  13. Nanostructured conducting polymer hydrogels for energy storage applications.

    Science.gov (United States)

    Shi, Ye; Peng, Lele; Yu, Guihua

    2015-08-14

    Conducting polymer hydrogels are emerging as a promising class of polymeric materials for various technological applications, especially for energy storage devices due to their unique combination of advantageous features of conventional polymers and organic conductors. To overcome the drawbacks of conventional synthesis, new synthetic routes in which acid molecules are adopted as both crosslinkers and dopants have been developed for conducting polymer hydrogels with unique 3D hierarchical porous nanostructures, resulting in high electrical conductivity, large surface area, structural tunability and hierarchical porosity for rapid mass/charge transport. The newly developed conducting polymer hydrogels exhibit high performance when applied as active electrode materials for electrochemical capacitors or as functional binder materials for high-energy lithium-ion batteries. This feature article summarizes the synthesis of conducting polymer hydrogels, presents their applications in energy storage, and discusses further opportunities and challenges.

  14. Concept of porous wire anemometer

    Energy Technology Data Exchange (ETDEWEB)

    Afgan, N.H.; Pereira, J.C. [Inst. Superior Tecnico, Lisbon (Portugal); Leontiev, A.I.; Puzach, S.V. [Moscow Technical Univ. (Russian Federation)

    1997-05-01

    The paper presents a new scheme of the anemometer sensing element for the gas mean and fluctuation velocity measurement. The sensing element is a porous tube with gas suction through porous tube wall. The outside surface of the porous tube is at the gas temperature. The analysis, based on the heat balance at steady and unsteady state is performed in order to define the sensitivity and time constant of the porous sensing element. Two cases are considered, namely, the constant current and constant temperature anemometer. Comparison is made with the solid wire anemometer and shown that the proposed porous sensing element can have sensitivity four times higher than the standard hot wire anemometer with the same geometrical dimensions. With the respective selection of the physical properties of the sensing element, it could be possible to obtain higher frequency range of the measurement. Particular attention is devoted to the low gas velocity measurement. It is recognized that the minimum gas velocity to be measured with the solid hot wire anemometer is determined by the local heat transfer coefficient. For the low gas velocity, it was proved that the minimum is around .20 cm/sec. The proposed concept of the sensing element can be used for the very low velocity measurement due to the higher sensitivity obtained by the porous sensing element.

  15. Load-Induced Hydrodynamic Lubrication of Porous Films.

    Science.gov (United States)

    Khosla, Tushar; Cremaldi, Joseph; Erickson, Jeffrey S; Pesika, Noshir S

    2015-08-19

    We present an exploratory study of the tribological properties and mechanisms of porous polymer surfaces under applied loads in aqueous media. We show how it is possible to change the lubrication regime from boundary lubrication to hydrodynamic lubrication even at relatively low shearing velocities by the addition of vertical pores to a compliant polymer. It is hypothesized that the compressed, pressurized liquid in the pores produces a repulsive hydrodynamic force as it extrudes from the pores. The presence of the fluid between two shearing surfaces results in low coefficients of friction (μ ≈ 0.31). The coefficient of friction is reduced further by using a boundary lubricant. The tribological properties are studied for a range of applied loads and shear velocities to demonstrate the potential applications of such materials in total joint replacement devices.

  16. Controlling shockwave dynamics using architecture in periodic porous materials

    Science.gov (United States)

    Branch, Brittany; Ionita, Axinte; Clements, Bradford E.; Montgomery, David S.; Jensen, Brian J.; Patterson, Brian; Schmalzer, Andrew; Mueller, Alexander; Dattelbaum, Dana M.

    2017-04-01

    Additive manufacturing (AM) is an attractive approach for the design and fabrication of structures capable of achieving controlled mechanical response of the underlying deformation mechanisms. While there are numerous examples illustrating how the quasi-static mechanical responses of polymer foams have been tailored by additive manufacturing, there is limited understanding of the response of these materials under shockwave compression. Dynamic compression experiments coupled with time-resolved X-ray imaging were performed to obtain insights into the in situ evolution of shockwave coupling to porous, periodic polymer foams. We further demonstrate shock wave modulation or "spatially graded-flow" in shock-driven experiments via the spatial control of layer symmetries afforded by additive manufacturing techniques at the micron scale.

  17. Facile fabrication and adsorption property of a nano/microporous coordination polymer with controllable size and morphology.

    Science.gov (United States)

    Liu, Qing; Jin, Li-Na; Sun, Wei-Yin

    2012-09-11

    A porous coordination polymer [Cu(3)(btc)(2)] with controllable size and morphology from nanocube to microoctahedron was readily synthesized in an ethanol-water mixture at room temperature by adjusting the concentration of the surfactant and the polymer shows size- and morphology-dependent sorption properties.

  18. Porous Membranes Built Up from Hydrophilic Poly(ionic liquid)s.

    Science.gov (United States)

    Täuber, Karoline; Zimathies, Annett; Yuan, Jiayin

    2015-12-01

    Porous polymer membranes made via electrostatic complexation are fabricated from a water-soluble poly(ionic liquid) (PIL) for the first time. The porous structure is formed as a consequence of simultaneous phase separation of the PIL and ionic complexation with an acid, which occurred in a basic solution of a nonsolvent for the PIL. These membranes have a stimuli-responsive porosity, with open and closed pores in isopropanol and in water, respectively. This property is quantitatively demonstrated in filtration experiments, where water is passing much slower through the membranes than isopropanol.

  19. Preparation and hydrogen storage capacity of highly porous activated carbon materials derived from polythiophene

    OpenAIRE

    2011-01-01

    [EN] Highly porous carbons have been successfully synthesized by chemical activation of polythiophene with KOH. The activation process was performed under relatively mild activation conditions, i. e., a KOH/polymer weight ratio of 2 and reaction temperatures in the 600–850 °C range. The porous carbons thus obtained possess very large surface areas, up to 3000 m2/g, and pore volumes of up to 1.75 cm3/g. The pore size distribution of these carbons can be tuned via modification of the activation...

  20. On effective transport coefficients in PEM fuel cell electrodes: Anisotropy of the porous transport layers

    Science.gov (United States)

    Pharoah, J. G.; Karan, K.; Sun, W.

    This paper reviews the approach taken in the literature to model the effective transport coefficients - mass diffusivity, electrical conductivity, thermal conductivity and hydraulic permeability - of carbon-fibre based porous electrode of polymer electrolyte membrane fuel cells (PEMFCs). It is concluded that current PEMFC model do not account for the inherent anisotropic microstructure of the fibrous electrodes. Simulations using a 2-D PEMFC cathode model show that neglecting the anisotropic nature and associated transport coefficients of the porous electrodes significantly influences both the nature and the magnitude of the model predictions. This emphasizes the need to appropriately characterize the relevant anisotropic properties of the fibrous electrode.

  1. Synthesis and gas adsorption study of porous metal-organic framework materials

    Science.gov (United States)

    Mu, Bin

    Metal-organic frameworks (MOFs) or porous coordination polymers (PCPs) have become the focus of intense study over the past decade due to their potential for advancing a variety of applications including air purification, gas storage, adsorption separations, catalysis, gas sensing, drug delivery, and so on. These materials have some distinct advantages over traditional porous materials such as the well-defined structures, uniform pore sizes, chemically functionalized sorption sites, and potential for postsynthetic modification, etc. Thus, synthesis and adsorption studies of porous MOFs have increased substantially in recent years. Among various prospective applications, air purification is one of the most immediate concerns, which has urgent requirements to improve current nuclear, biological, and chemical (NBC) filters involving commercial and military purposes. Thus, the major goal of this funded project is to search, synthesize, and test these novel hybrid porous materials for adsorptive removal of toxic industrial chemicals (TICs) and chemical warfare agents (CWAs), and to install the benchmark for new-generation NBC filters. The objective of this study is three-fold: (i) Advance our understanding of coordination chemistry by synthesizing novel MOFs and characterizing these porous coordination polymers; (ii) Evaluate porous MOF materials for gasadsorption applications including CO2 capture, CH4 storage, other light gas adsorption and separations, and examine the chemical and physical properties of these solid adsorbents including thermal stability and heat capacity of MOFs; (iii) Evaluate porous MOF materials for next-generation NBC filter media by adsorption breakthrough measurements of TICs on MOFs, and advance our understanding about structureproperty relationships of these novel adsorbents.

  2. A POROUS, LAYERED HELIOPAUSE

    Energy Technology Data Exchange (ETDEWEB)

    Swisdak, M.; Drake, J. F. [Institute for Research in Electronics and Applied Physics, University of Maryland, College Park, MD 20742 (United States); Opher, M., E-mail: swisdak@umd.edu, E-mail: drake@umd.edu, E-mail: mopher@bu.edu [Department of Astronomy, Boston University, 725 Commonwealth Avenue, Boston, MA 02215 (United States)

    2013-09-01

    The picture of the heliopause (HP)-the boundary between the domains of the Sun and the local interstellar medium (LISM)-as a pristine interface with a large rotation in the magnetic field fails to describe recent Voyager 1 (V1) data. Magnetohydrodynamic (MHD) simulations of the global heliosphere reveal that the rotation angle of the magnetic field across the HP at V1 is small. Particle-in-cell simulations, based on cuts through the MHD model at V1's location, suggest that the sectored region of the heliosheath (HS) produces large-scale magnetic islands that reconnect with the interstellar magnetic field while mixing LISM and HS plasma. Cuts across the simulation reveal multiple, anti-correlated jumps in the number densities of LISM and HS particles, similar to those observed, at the magnetic separatrices. A model is presented, based on both the observations and simulations, of the HP as a porous, multi-layered structure threaded by magnetic fields. This model further suggests that contrary to the conclusions of recent papers, V1 has already crossed the HP.

  3. Polymer blends

    Energy Technology Data Exchange (ETDEWEB)

    Allen, Scott D.; Naik, Sanjeev

    2017-08-22

    The present invention provides, among other things, extruded blends of aliphatic polycarbonates and polyolefins. In one aspect, provided blends comprise aliphatic polycarbonates such as poly(propylene carbonate) and a lesser amount of a crystalline or semicrystalline polymer. In certain embodiments, provided blends are characterized in that they exhibit unexpected improvements in their elongation properties. In another aspect, the invention provides methods of making such materials and applications of the materials in applications such as the manufacture of consumer packaging materials.

  4. Fabrication of highly porous biodegradable biomimetic nanocomposite as advanced bone tissue scaffold

    Directory of Open Access Journals (Sweden)

    Abdalla Abdal-hay

    2017-02-01

    Full Text Available Development of bioinspired or biomimetic materials is currently a challenge in the field of tissue regeneration. In-situ 3D biomimetic microporous nanocomposite scaffold has been developed using a simple lyophilization post hydrothermal reaction for bone healing applications. The fabricated 3D porous scaffold possesses advantages of good bonelike apatite particles distribution, thermal properties and high porous interconnected network structure. High dispersion bonelike apatite nanoparticles (NPs rapidly nucleated and deposited from surrounding biological minerals within chitosan (CTS matrices using hydrothermal technique. After that, freeze-drying method was applied on the composite solution to form the desired porous 3D architecture. Interestingly, the porosity and pore size of composite scaffold were not significantly affected by the particles size and particles content within the CTS matrix. Our results demonstrated that the compression modulus of porous composite scaffold is twice higher than that of plain CTS scaffold, indicating a maximization of the chemical interaction between polymer matrix and apatite NPs. Cytocompatibility test for MC3T3-E1 pre-osteoblasts cell line using MTT-indirect assay test showed that the fabricated 3D microporous nanocomposite scaffold possesses higher cell proliferation and growth than that of pure CTS scaffold. Collectively, our results suggest that the newly developed highly porous apatite/CTS nanocomposite scaffold as an alternative of hydroxyapatite/CTS scaffold may serve as an excellent porous 3D platform for bone tissue regeneration.

  5. Preparation of porous carboxymethyl chitosan grafted poly (acrylic acid) superabsorbent by solvent precipitation and its application as a hemostatic wound dressing.

    Science.gov (United States)

    Chen, Yu; Zhang, Yong; Wang, Fengju; Meng, Weiwei; Yang, Xinlin; Li, Peng; Jiang, Jianxin; Tan, Huimin; Zheng, Yongfa

    2016-06-01

    The volume phase transition of a hydrogel initiated by shrinking may result in complex patterns on its surface. Based on this unique property of hydrogel, we have developed a novel solvent precipitation method to prepare a kind of novel superabsorbent polymers with excellent hemostatic properties. A porous carboxymethyl chitosan grafted poly (acrylic acid) (CMCTS-g-PAA) superabsorbent polymer was prepared by precipitating CMCTS-g-PAA hydrogel with ethanol. Its potential application in hemostatic wound dressing was investigated. The results indicate that the modified superabsorbent polymer is non-cytotoxic. It showed a high swelling capacity and better hemostatic performance in the treatments of hemorrhage model of ear artery, arteria cruralis and spleen of the New Zealand white rabbit than the unmodified polymer and other commonly used clinic wound dressings. The hemostatic mechanism of the porous CMCTS-g-PAA polymer was also discussed.

  6. Preparation of porous carboxymethyl chitosan grafted poly (acrylic acid) superabsorbent by solvent precipitation and its application as a hemostatic wound dressing

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Yu, E-mail: cylsy@163.com [School of Material Science and Engineering, Beijing Institute of Technology, Beijing 100081 (China); Zhang, Yong [School of Life Science, Beijing Institute of Technology, Beijing 100081 (China); Wang, Fengju [School of Material Science and Engineering, Beijing Institute of Technology, Beijing 100081 (China); Meng, Weiwei; Yang, Xinlin [School of Life Science, Beijing Institute of Technology, Beijing 100081 (China); Li, Peng [School of Material Science and Engineering, Beijing Institute of Technology, Beijing 100081 (China); Jiang, Jianxin [State Key Laboratory of Trauma Burns and Combined Injury, The Third Military Medical University, Chongqing 400042 (China); Tan, Huimin [School of Material Science and Engineering, Beijing Institute of Technology, Beijing 100081 (China); Zheng, Yongfa [Guangdong Fuyang Biotechnology Co., Ltd., Heyuan, Guangdong 517000 (China)

    2016-06-01

    The volume phase transition of a hydrogel initiated by shrinking may result in complex patterns on its surface. Based on this unique property of hydrogel, we have developed a novel solvent precipitation method to prepare a kind of novel superabsorbent polymers with excellent hemostatic properties. A porous carboxymethyl chitosan grafted poly (acrylic acid) (CMCTS-g-PAA) superabsorbent polymer was prepared by precipitating CMCTS-g-PAA hydrogel with ethanol. Its potential application in hemostatic wound dressing was investigated. The results indicate that the modified superabsorbent polymer is non-cytotoxic. It showed a high swelling capacity and better hemostatic performance in the treatments of hemorrhage model of ear artery, arteria cruralis and spleen of the New Zealand white rabbit than the unmodified polymer and other commonly used clinic wound dressings. The hemostatic mechanism of the porous CMCTS-g-PAA polymer was also discussed. - Highlights: • The novel solvent precipitation method was developed to prepare the porous superabsorbent polymer. • The swelling rate was promoted and the harmful residual monomer was leached after modification. • The modified polymer showed good biological safety. • It showed good hemostasis to arterial hemorrhage model of the animal. • The hemostatic mechanism of the modified superabsorbent polymer was discussed.

  7. Polymer/Solvent and Polymer/Polymer Interaction Studies

    Science.gov (United States)

    1980-09-01

    DCM and ATS are completely miscible. The sorption data described 1 2Jones, E. G., Pedrick , D. L., and Benadum, P. A., Polymer Characteri- zation Using...Encyclopedia of Polymer Science and Technology, Vol. 11, Wiley-Interscience, N.Y. (1969), p. 447. 12. Jones, E.G., Pedrick , D.L., and Benadum, P.A., Polymer

  8. Conjugated microporous polymers: design, synthesis and application.

    Science.gov (United States)

    Xu, Yanhong; Jin, Shangbin; Xu, Hong; Nagai, Atsushi; Jiang, Donglin

    2013-10-21

    Conjugated microporous polymers (CMPs) are a class of organic porous polymers that combine π-conjugated skeletons with permanent nanopores, in sharp contrast to other porous materials that are not π-conjugated and with conventional conjugated polymers that are nonporous. As an emerging material platform, CMPs offer a high flexibility for the molecular design of conjugated skeletons and nanopores. Various chemical reactions, building blocks and synthetic methods have been developed and a broad variety of CMPs with different structures and specific properties have been synthesized, driving the rapid growth of the field. CMPs are unique in that they allow the complementary utilization of π-conjugated skeletons and nanopores for functional exploration; they have shown great potential for challenging energy and environmental issues, as exemplified by their excellent performance in gas adsorption, heterogeneous catalysis, light emitting, light harvesting and electrical energy storage. This review describes the molecular design principles of CMPs, advancements in synthetic and structural studies and the frontiers of functional exploration and potential applications.

  9. Preparation of porous poly(trimethylene carbonate structures for controlled release applications using high pressure CO2

    NARCIS (Netherlands)

    Nalawade, S.P.; Hennink, W.E.; Westerman, D.; Feijen, J.; Sam, A.P.; Leeke, G.; Santos, R.C.D.; Grijpma, Dirk W.; Feijen, Jan

    2008-01-01

    Porous poly(trimethylene carbonate) structures can readily be prepared using high pressure CO2. Differences in CO2 solubility in the polymer matrix at the different processing temperatures and pressures lead to different pore morphologies upon depressurization. Furthermore, crystallization of the

  10. Preparation of porous poly(trimethylene carbonate) structures for controlled release applications using high pressure CO2

    NARCIS (Netherlands)

    Nalawade, S.P.; Westerman, D.; Leeke, G.; Santos, R.C.D.; Grijpma, D.W.; Feijen, J.

    2008-01-01

    Porous poly(trimethylene carbonate) structures can readily be prepared using high pressure CO2. Differences in CO2 solubility in the polymer matrix at the different processing temperatures and pressures lead to different pore morphologies upon depressurization. Furthermore, crystallization of the in

  11. Constructing Post-Permeation Method to Fabricate Polymer/Nanocrystals Hybrid Solar Cells with PCE Exceeding 6.

    Science.gov (United States)

    Du, Xiaohang; Zeng, Qingsen; Jin, Gan; Liu, Fangyuan; Ji, Tianjiao; Yue, Yuanyuan; Yang, Yi; Zhang, Hao; Yang, Bai

    2017-01-11

    A post-permeation method is constructed for fabricating bulk-heterojunction hybrid solar cells. Porous CdTe film is prepared by annealing the mixture solution of aqueous CdTe nanocrystals and cetyltrimethyl ammonium bromide, after which the post-permeation of polymer is employed. By this method, kinds of polymers can be applied regardless of the intermiscibility with the nanoparticles. The inorganic nanocrystals and the polymer can be treated under respective optimized annealing temperatures, which can facilitate the growth of nanocrystals without damaging the polymers. A high power conversion efficiency of 6.36% in the polymer/nanocrystals hybrid solar cells is obtained via systematical optimization.

  12. Plasmon assisted synthesis of highly fluorescing silver quantum cluster/polymer composites for biochemical sensing

    DEFF Research Database (Denmark)

    Bernard, S.; Kutter, J. P.; Mogensen, K. B.

    2014-01-01

    Plasmonics is combined with polymer synthesis for rapid fabrication of highly fluorescing silver quantum cluster/polymer composites inside microfluidic channels. UV-light assisted synthesis of polymers has been investigated by a number of groups previously [1], however, plasmon assisted synthesis...... has not been presented before. This should allow highly localized fabrication of porous polymers that are defined by the location of the nanoplasmonic metal film. Silver quantum clusters (AgQCs) consisting of 2-10 atoms can be highly fluorescing in the visible wavelength range and possess a greater...

  13. Nanoporous materials modified with biodegradable polymers as models for drug delivery applications

    DEFF Research Database (Denmark)

    Gruber, Mathias F; Schulte, Lars; Ndoni, Sokol

    2013-01-01

    Polymers play a central role in the development of carriers for diagnostic and therapeutic agents. Especially the use of either degradable polymers or porous materials to encapsulate drug compounds in order to obtain steady drug release profiles has received much attention. We present here a proof...... of principle for a system combining these two encapsulation methods and consisting of a nanoporous polymer (NP) with the pores filled with a degradable polymer mixed with a drug model. Rhodamine 6G (R6G) mixed with Poly(l-Lactic Acid) (PLLA) were confined within the 14nm pores of a NP with gyroid morphology...

  14. Plasmon assisted synthesis of highly fluorescing silver quantum cluster / polymer composites for biochemical sensing

    DEFF Research Database (Denmark)

    Bernard, S.; Kutter, J.P.; Mogensen, Klaus Bo

    2014-01-01

    has not been presented before. This should allow highly localized fabrication of porous polymers that are defined by the location of the nanoplasmonic metal film. Silver quantum clusters (AgQCs) consisting of 2-10 atoms can be highly fluorescing in the visible wavelength range and possess a much......Plasmonics is combined with polymer synthesis for rapid fabrication of highly fluorescing silver quantum cluster / polymer composites inside microfluidic channels. UV-light assisted synthesis of polymers has been investigated by a number of groups previously [1], however, plasmon assisted synthesis...

  15. Porous microsphere and its applications

    Directory of Open Access Journals (Sweden)

    Cai Y

    2013-03-01

    Full Text Available Yunpeng Cai,1,2* Yinghui Chen,3* Xiaoyun Hong,2 Zhenguo Liu,1 Weien Yuan2 1Department of Neurology, Xinhua Hospital affiliated to Shanghai Jiaotong University School of Medicine, 2School of Pharmacy, Shanghai JiaoTong University, 3Department of Neurology Jinshan Hospital, Fudan University, Shanghai, People's Republic of China *These authors contributed equally to this workAbstract: Porous microspheres have drawn great attention in the last two decades for their potential applications in many fields, such as carriers for drugs, absorption and desorption of substances, pulmonary drug delivery, and tissue regeneration. The application of porous microspheres has become a feasible way to address existing problems. In this essay, we give a brief introduction of the porous microsphere, its characteristics, preparation methods, applications, and a brief summary of existing problems and research tendencies.Keywords: pore, porosity, porogen, suspension polymerization, seed swelling, pulmonary drug delivery, tissue regeneration

  16. Formation of porous gas hydrates

    CERN Document Server

    Salamatin, Andrey N

    2015-01-01

    Gas hydrates grown at gas-ice interfaces are examined by electron microscopy and found to have a submicron porous texture. Permeability of the intervening hydrate layers provides the connection between the two counterparts (gas and water molecules) of the clathration reaction and makes further hydrate formation possible. The study is focused on phenomenological description of principal stages and rate-limiting processes that control the kinetics of the porous gas hydrate crystal growth from ice powders. Although the detailed physical mechanisms involved in the porous hydrate formation still are not fully understood, the initial stage of hydrate film spreading over the ice surface should be distinguished from the subsequent stage which is presumably limited by the clathration reaction at the ice-hydrate interface and develops after the ice grain coating is finished. The model reveals a time dependence of the reaction degree essentially different from that when the rate-limiting step of the hydrate formation at...

  17. Nonequilibrium Thermodynamics of Porous Electrodes

    CERN Document Server

    Ferguson, Todd R

    2012-01-01

    We review classical porous electrode theory and extend it to non-ideal active materials, including those capable of phase transformations. Using principles of non-equilibrium thermodynamics, we relate the cell voltage, ionic fluxes, and Faradaic charge-transfer kinetics to the variational electrochemical potentials of ions and electrons. The Butler-Volmer exchange current is consistently expressed in terms of the activities of the reduced, oxidized and transition states, and the activation overpotential is defined relative to the local Nernst potential. We also apply mathematical bounds on effective diffusivity to estimate porosity and tortuosity corrections. The theory is illustrated for a Li-ion battery with active solid particles described by a Cahn-Hilliard phase-field model. Depending on the applied current and porous electrode properties, the dynamics can be limited by electrolyte transport, solid diffusion and phase separation, or intercalation kinetics. In phase-separating porous electrodes, the model...

  18. On strength of porous material

    DEFF Research Database (Denmark)

    Nielsen, Lauge Fuglsang

    1999-01-01

    quality without damaging or destroying the material or the building component considered. The efficiency of MOE-MOR relations for this purpose depends very much on the homogeneity of porous material considered. For building materials like wood and concrete of normal or lower quality with a number......The question of non-destructive testing of porous materials has always been of interest for the engineering profession. A number of empirically based MOE-MOR relations between stiffness (Modulus Of Elasticity) and strength (Modulus OF Rupture) of materials have been established in order to control...... of irregularities only scattered MOE-MOR relations (clouds) can be established from which no really results can be read.For homogeneously produced porous materials, however, like modern ceramics and high performance concretes MOE-MOR relations can be presented which are reliable. The present paper contributes...

  19. Acoustic Absorption in Porous Materials

    Science.gov (United States)

    Kuczmarski, Maria A.; Johnston, James C.

    2011-01-01

    An understanding of both the areas of materials science and acoustics is necessary to successfully develop materials for acoustic absorption applications. This paper presents the basic knowledge and approaches for determining the acoustic performance of porous materials in a manner that will help materials researchers new to this area gain the understanding and skills necessary to make meaningful contributions to this field of study. Beginning with the basics and making as few assumptions as possible, this paper reviews relevant topics in the acoustic performance of porous materials, which are often used to make acoustic bulk absorbers, moving from the physics of sound wave interactions with porous materials to measurement techniques for flow resistivity, characteristic impedance, and wavenumber.

  20. Plasma deposited fluorinated films on porous membranes

    Energy Technology Data Exchange (ETDEWEB)

    Gancarz, Irena [Department of Polymer and Carbon Materials, Wrocław University of Technology, 50-370 Wrocław (Poland); Bryjak, Marek, E-mail: marek.bryjak@pwr.edu.pl [Department of Polymer and Carbon Materials, Wrocław University of Technology, 50-370 Wrocław (Poland); Kujawski, Jan; Wolska, Joanna [Department of Polymer and Carbon Materials, Wrocław University of Technology, 50-370 Wrocław (Poland); Kujawa, Joanna; Kujawski, Wojciech [Nicolaus Copernicus University, Faculty of Chemistry, 7 Gagarina St., 87-100 Torun (Poland)

    2015-02-01

    75 KHz plasma was used to modify track etched poly(ethylene terephthalate) membranes and deposit on them flouropolymers. Two fluorine bearing monomers were used: perflourohexane and hexafluorobenzene. The modified surfaces were analyzed by means of attenuated total reflection infra-red spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, atomic force microscopy and wettability. It was detected that hexaflourobenxene deposited to the larger extent than perflourohaxane did. The roughness of surfaces decreased when more fluoropolymer was deposited. The hydrophobic character of surface slightly disappeared during 20-days storage of hexaflourobenzene modified membrane. Perfluorohexane modified membrane did not change its character within 120 days after modification. It was expected that this phenomenon resulted from post-reactions of oxygen with radicals in polymer deposits. The obtained membranes could be used for membrane distillation of juices. - Highlights: • Plasma deposited hydrophobic layer of flouropolymers. • Deposition degree affects the surface properties. • Hydrohilization of surface due to reaction of oxygen with entrapped radicals. • Possibility to use modified porous membrane for water distillation and apple juice concentration.

  1. Hydrothermal synthesis of 3D porous architectures

    Institute of Scientific and Technical Information of China (English)

    XIAO Wanyan; GU Xiaojun; XUE Dongfeng

    2009-01-01

    A novel porous lanthanide-organic coordination polymer, [Nd(H2O)(HnicO)(TP)]·2H2O (1) (H2nicO=2-hydroxynieotinic acid, TP= terephthalate), was prepared under hydrothermai condition and characterized by single-crystal X-ray diffraction, thermogravimetrie analysis and infrared spectroscopy. Compound 1 exhibited a flexible coordination geometry of lanthanide ions, which possessed a three-dimensional (3D) open framework with one-dimensional (1D) channels containing lattice water molecules. This framework structure exhibited a high stability up to 330 ℃ after removing free water molecules. A homometallic supramolecular framework (Zn(HnicO)2(H2O)2 (2)) was obtained due to the competitive reaction between organic ligands, Nd3+ and Zn2+ ions. The results showed that on the basis of the soft-hard/acid-base principle the coordination selection between metal ions and organic ligands played an essential role in the smart construc-tion of lanthanide architectures.

  2. Composite polymer electrolyte membranes supported by non-woven fabrics for lithium-ion polymer batteries

    Institute of Scientific and Technical Information of China (English)

    TANG Dingguo; LIU Jianhong; QI Lu; CHEN Hui; CI Yunxiang

    2005-01-01

    Poly(vinylidene fluoride-co-hexafluoropropyle- ne) (PVDF-HFP) is one of the most popular polymers for polymer electrolyte membranes because of its excellent operating characteristics and superior electrochemical properties. The electrochemical performances of polymer electrolyte membrane can be enhanced by evenly dispersing nano-meter SiO2 particles in the polymer. In this paper, non-woven fabrics were immersed in the mixed solution of PVDF-HFP/ SiO2/butanone/butanol/plasticizer, and then dried in a vacuum oven to remove the solvents and the plasticizer and to make porous composite polymer electrolyte membranes. The prepared composite membranes supported by non-woven fabrics boast good mechanical strength and excellent electrochemical properties: the electrochemical stability window is 4.8 V vs. Li+/Li, and the ionic conductivity is 3.35×10-4 S/cm (around 60% of that of a common PE membrane) at room temperature. The lithium-ion polymer battery assembled by the composite membrane exhibits high rate capability and excellent cycling performance.

  3. Integrated Analysis of Permeability Reduction Caused by Polymer Retention for Better Understanding Polymer Transport

    Directory of Open Access Journals (Sweden)

    ByungIn Choi

    2015-01-01

    Full Text Available Polymer retention is one of the most important factors to govern polymer propagation through porous media, determining whether successful or not. The focus of previous studies has been limited to polymer concentration loss caused by the retention; not only change in polymer concentration, but also reduction in reservoir permeability is the main issue for theoretical transport study. Due to the lack of accuracy of Langmuir isotherm describing the polymer retention mechanisms, this study proposes a new type of matching interpretation method to correlate the permeability reduction factors from experiments to permeability. In order to solve the problem of poorly matching results between estimation and observation, use of nonadsorptive constant conditionally selected in matching process was made. Based on the threshold permeability reduction factors, approximate critical permeability can be calculated to which nonadsorptive constant would be applied. Results showed significant improvements in the estimation of permeability reduction for both low and high permeability cores. In addition, effects of permeability reduction on polymer transport in field scale were analyzed using the proposed matching model. Thus, not only does this interpretation method help to evaluate prediction for accurate flow behavior, but also unwanted risk can be evaluated.

  4. Effects of Porous Throat on Transonic Diffuser

    OpenAIRE

    屋我, 実; 永井, 實; 富田, 教夫; 芳賀, 剛; 宮良, 透; Yaga, Minoru; Nagai, Minoru; Tomita, Norio; Haga, Tsuyoshi; Miyara, Tooru

    1995-01-01

    The effects of the porous throat on a transonic diffuser were investigated experimentally by wall static pressure measurements and by schlieren optical observations. The porous throat consists of a wall with 126 holes and a cavity underneath it so that the flow around the shock wave can circulate through the porous wall. The results show that no shock wave was observed at 80% of the porous region from the throat and that the pressure fluctuations in the transonic diffuser were greatly reduced...

  5. Luminescence decay of porous silicon

    Science.gov (United States)

    Chen, X.; Uttamchandani, D.; Sander, D.; O'Donnell, K. P.

    1993-04-01

    The luminescence decay pattern of porous silicon samples prepared by electrochemical etching is characterised experimentally by a non-exponential profile, a strong dependence on temperature and an absence of spectral diffusion. We describe this luminescence as carrier-dopping-assisted recombination. Following the correlation function approach to non-dispersive transport developed by Scher and co-workers [Physics Today 41 (1991) 26], we suggest a simple derivation of analytical functions which accurately describes the anomalous luminescence decay of porous silicon, and show that this model includes exponential and Kohlrausch [Pogg. Ann. Phys. 119 (1863) 352] (stretched-exponential) relaxations as special cases.

  6. Porous Materials - Structure and Properties

    DEFF Research Database (Denmark)

    Nielsen, Anders

    1997-01-01

    The paper presents some viewpoints on the description of the pore structure and the modelling of the properties of the porous building materials. Two examples are given , where it has been possible to connect the pore structure to the properties: Shrinkage of autoclaved aerated concrete and the p......The paper presents some viewpoints on the description of the pore structure and the modelling of the properties of the porous building materials. Two examples are given , where it has been possible to connect the pore structure to the properties: Shrinkage of autoclaved aerated concrete...

  7. Drastic difference in porous structure of calcium alginate microspheres prepared with fresh or hydrolyzed sodium alginate.

    Science.gov (United States)

    Akamatsu, Kazuki; Maruyama, Kaho; Chen, Wei; Nakao, Aiko; Nakao, Shin-ichi

    2011-11-15

    Fresh or hydrolyzed sodium alginate was used as a material for preparing calcium alginate microspheres, and a drastic difference in porous structure was observed between them, even though the other materials and the preparation method except for the sodium alginate were exactly the same. When fresh sodium alginate was used, nonporous microspheres were obtained. In contrast, when 82-day-hydrolyzed sodium alginate, whose molecular weight became 7% of the molecular weight of the fresh sodium alginate, was used, porous microspheres with 6.5 times larger BET surface area were obtained. XPS studies indicated that the atomic ratio of Ca, the crosslinker of the alginic acid polymer, was almost the same in both cases. Therefore, the difference in porous structure was not attributed to the amount of crosslinking points, but to the low-molecular-weight compounds formed by hydrolysis, and they would work as pore-generating agents. Copyright © 2011 Elsevier Inc. All rights reserved.

  8. Sol-gel derived porous bioactive nanocomposites: Synthesis and in vitro bioactivity

    Science.gov (United States)

    Shankhwar, Nisha; Kothiyal, G. P.; Srinivasan, A.

    2013-06-01

    Porous bioactive composites consisting of SiO2-CaO-Na2O-P2O5 bioactive glass-ceramic and synthetic water soluble polymer Polyvinylpyrrolidone [PVP (C6H9NO)n, MW˜40000 g/mol] have been synthesized by sol-gel route. As-prepared polymeric composites were characterized by X-ray diffraction (XRD) technique. Two major bone mineral phases, viz., hydroxyapatite [Ca10(PO4)6(OH)2] and wollastonite [calcium silicate (CaSiO3)] have been identified in the XRD patterns of the composites. Presence of these bone minerals indicates the bioactive nature of the composites. In vitro bioactivity tests confirm bioactivity in the porous composites. The flexibility offered by these bioactive polymer composites is advantageous for its application as implant material.

  9. Comparison on mechanical properties of single layered and bilayered chitosan-gelatin coated porous hydroxyapatite scaffold prepared through freeze drying method

    Science.gov (United States)

    Effendi, M. D.; Gustiono, D.; Lukmana; Ayu, D.; Kurniawati, F.

    2017-02-01

    Biopolymer coated porous hydroxyapatite (HA) scaffolds were prepared for tissue engineering trough freeze drying method and impregnation. in this study, to mimic the mineral and organic component of natural bone, synthetic hydroxapatite (HA) scaffolds coated by polymer were prepared. Highly porous Hap scaffolds, fabricated by synthetic HA impregnation method on polyurethane foam, were coated with polymer coating solution, consisting of chitosan, Gelatin, and bilayered chitosan-gelatin prepared by aging and impregnating technique. For the purpose of comparison, The bare scaffolds without polymer coating layer were investigated. The Bare scaffolds were highly porous and interconnected with a pore size of around 150 µm–714 µm, has porosity at around 67,7% -85,7%, and has mechanical strength at around 0.06 Mpa - 0.071 Mpa, which is suitable for osteoblast cell Proliferation. Chitosan coated porous HA scaffold and gelatin coated porous HA scaffold had mechanical strength at around 0.81-0.85 Mpa, and 1.32-1.34 Mpa, respectively, with weight ratio of biopolymer and Hap was around 18%-22%. To compare these results, the coating on the bare scaffold with gelatin and chitosan had been conducted. Based on the result of FTIR, it could be concluded that coating procedure applied on porous hydroxy apatite (HA) coated by gelatin, chitosan coated HA scaffold, and bilayered Gelatin-chitosan coated porous HA scaffold, confirming that for allsampleshad no significant chemical effect on the coating structure. The compressive strength of bilayered Gelatin-chitosan coated HA scaffold had middle values between the rest, at around 1,06-1.2 Mpa for the samples at the same weight ratio of biopolymer: HA (around 18% - 22%). These results also confirming that coating by gelatin on porous hydroxyapatite was highest compresive strength and can be applied to improve mechanical properties of porous hydroxyapatite bare scaffold

  10. Fabrication of a porous fiber cladding material using microsphere templating for improved response time with fiber optic sensor arrays.

    Science.gov (United States)

    Henning, Paul E; Rigo, M Veronica; Geissinger, Peter

    2012-01-01

    A highly porous optical-fiber cladding was developed for evanescent-wave fiber sensors, which contains sensor molecules, maintains guiding conditions in the optical fiber, and is suitable for sensing in aqueous environments. To make the cladding material (a poly(ethylene) glycol diacrylate (PEGDA) polymer) highly porous, a microsphere templating strategy was employed. The resulting pore network increases transport of the target analyte to the sensor molecules located in the cladding, which improves the sensor response time. This was demonstrated using fluorescein-based pH sensor molecules, which were covalently attached to the cladding material. Scanning electron microscopy was used to examine the structure of the templated polymer and the large network of interconnected pores. Fluorescence measurements showed a tenfold improvement in the response time for the templated polymer and a reliable pH response over a pH range of five to nine with an estimated accuracy of 0.08 pH units.

  11. Restructuring of porous nickel electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Lenhart, S.J.; Macdonald, D.D.; Pound, B.G.

    1984-08-01

    A transmission line model for the electrochemical impedance of porous electrodes was used to study the degradation of nickel battery plates throughout their cycle life. The model was shown to successfully account for changes in the observed electrode properties in terms of simultaneous restructuring of the active mass and rupture of particleparticle ohmic contacts.

  12. Additively manufactured porous tantalum implants

    NARCIS (Netherlands)

    Wauthle, Ruben; Van Der Stok, Johan; Yavari, Saber Amin; Van Humbeeck, Jan; Kruth, Jean Pierre; Zadpoor, Amir Abbas; Weinans, Harrie; Mulier, Michiel; Schrooten, Jan

    2015-01-01

    The medical device industry's interest in open porous, metallic biomaterials has increased in response to additive manufacturing techniques enabling the production of complex shapes that cannot be produced with conventional techniques. Tantalum is an important metal for medical devices because of it

  13. Plasmon assisted synthesis of highly fluorescing silver quantum cluster/polymer composites for biochemical sensing

    DEFF Research Database (Denmark)

    Bernard, S.; Kutter, J. P.; Mogensen, K. B.

    2014-01-01

    has not been presented before. This should allow highly localized fabrication of porous polymers that are defined by the location of the nanoplasmonic metal film. Silver quantum clusters (AgQCs) consisting of 2-10 atoms can be highly fluorescing in the visible wavelength range and possess a greater......Plasmonics is combined with polymer synthesis for rapid fabrication of highly fluorescing silver quantum cluster/polymer composites inside microfluidic channels. UV-light assisted synthesis of polymers has been investigated by a number of groups previously [1], however, plasmon assisted synthesis...... photostability than organic fluorophores [2]. In this work AgQCs are embedded into the oligoaniline porous matrix and is tested for indirect fluorescence detection of cyanide in a simple microfluidic device (Fig. 1). Imaging of individual silver clusters inside the channel (Fig. 1) is made possible by using 100x...

  14. Functional Ag porous films prepared by electrospinning

    Science.gov (United States)

    Dong, Guoping; Xiao, Xiudi; Liu, Xiaofeng; Qian, Bin; Liao, Yang; Wang, Chen; Chen, Danping; Qiu, Jianrong

    2009-06-01

    Face-centered cubic Ag porous films have been prepared directly from the heat treatment of AgNO 3-doped poly(vinyl alcohol) (PVA) electrospun nanofibers. Using Rhodamine B (RB) as the probing molecule, the surface-enhanced Raman scattering (SERS) effect of Ag porous films was demonstrated. The antibacterial activity of Ag porous films was also studied in this work. The propagation and biological activity of yeast cells were effectively inhibited by Ag porous films. These functional Ag porous films were expected to be applied in many fields, such as catalysis, diagnostics, sensors and antibacterial, etc.

  15. Macroporous Monolithic Polymers: Preparation and Applications

    Directory of Open Access Journals (Sweden)

    Cecilia Inés Alvarez Igarzabal

    2009-12-01

    Full Text Available In the last years, macroporous monolithic materials have been introduced as a new and useful generation of polymers used in different fields. These polymers may be prepared in a simple way from a homogenous mixture into a mold and contain large interconnected pores or channels allowing for high flow rates at moderate pressures. Due to their porous characteristics, they could be used in different processes, such as stationary phases for different types of chromatography, high-throughput bioreactors and in microfluidic chip applications. This review reports the contributions of several groups working in the preparation of different macroporous monoliths and their modification by immobilization of specific ligands on the products for specific purposes.

  16. Performance of polymer nano composite membrane electrode assembly using Alginate as a dopant in polymer electrolyte membrane fuel cell

    Science.gov (United States)

    Mulijani, S.

    2017-01-01

    Polymer membrane and composite polymer for membrane electrode assembly (MEAs) are synthesized and studied for usage in direct methanol fuel cell (DMFC). In this study, we prepared 3 type of MEAs, polystyrene (PS), sulfonated polystyrene (SPS) and composite polymer SPS-alginat membrane via catalyst hot pressed method. The performance and properties of prepared MEAs were evaluated and analyzed by impedance spectrometry and scanning electron microscopy (SEM). The result showed that, water up take of MEA composite polymer SPS-alginate was obtained higher than that in SPS and PS. The proton conductivity of MEA-SPS-alginate was also higher than that PS and PSS. SEM characterization revealed that the intimate contact between the carbon catalyst layers (CL) and the membranes, and the uniformly porous structure correlate positively with the MEAs prepared by hot pressed method, exhibiting high performances for DMFC.

  17. Performance of polymer nano composite membrane electrode assembly using Alginate as a dopant in polymer electrolyte membrane fuel cell

    Science.gov (United States)

    Mulijani, S.

    2016-11-01

    Polymer membrane and composite polymer for membrane electrode assembly (MEAs) are synthesized and studied for usage in direct methanol fuel cell (DMFC). In this study, we prepared 3 type of MEAs, polystyrene (PS), sulfonated polystyrene (SPS) and composite polymer SPS-alginat membrane via catalyst hot pressed method. The performance and properties of prepared MEAs were evaluated and analyzed by impedance spectrometry and scanning electron microscopy (SEM). The result showed that, water up take of MEA composite polymer SPS-alginate was obtained higher than that in SPS and PS. The proton conductivity of MEA-SPS-alginate was also higher than that PS and PSS. SEM characterization revealed that the intimate contact between the carbon catalyst layers (CL) and the membranes, and the uniformly porous structure correlate positively with the MEAs prepared by hot pressed method, exhibiting high performances for DMFC.

  18. Flexible High-Energy Polymer-Electrolyte-Based Rechargeable Zinc-Air Batteries.

    Science.gov (United States)

    Fu, Jing; Lee, Dong Un; Hassan, Fathy Mohamed; Yang, Lin; Bai, Zhengyu; Park, Moon Gyu; Chen, Zhongwei

    2015-10-07

    A thin-film, flexible, and rechargeable zinc-air battery having high energy density is reported particularly for emerging portable and wearable electronic applications. This freeform battery design is the first demonstrated by sandwiching a porous-gelled polymer electrolyte with a freestanding zinc film and a bifunctional catalytic electrode film. The flexibility of both the electrode films and polymer electrolyte membrane gives great freedom in tailoring the battery geometry and performance.

  19. Shape memory polymers

    Energy Technology Data Exchange (ETDEWEB)

    Wilson, Thomas S.; Bearinger, Jane P.

    2017-08-29

    New shape memory polymer compositions, methods for synthesizing new shape memory polymers, and apparatus comprising an actuator and a shape memory polymer wherein the shape memory polymer comprises at least a portion of the actuator. A shape memory polymer comprising a polymer composition which physically forms a network structure wherein the polymer composition has shape-memory behavior and can be formed into a permanent primary shape, re-formed into a stable secondary shape, and controllably actuated to recover the permanent primary shape. Polymers have optimal aliphatic network structures due to minimization of dangling chains by using monomers that are symmetrical and that have matching amine and hydroxl groups providing polymers and polymer foams with clarity, tight (narrow temperature range) single transitions, and high shape recovery and recovery force that are especially useful for implanting in the human body.

  20. Shape memory polymers

    Science.gov (United States)

    Wilson, Thomas S.; Bearinger, Jane P.

    2015-06-09

    New shape memory polymer compositions, methods for synthesizing new shape memory polymers, and apparatus comprising an actuator and a shape memory polymer wherein the shape memory polymer comprises at least a portion of the actuator. A shape memory polymer comprising a polymer composition which physically forms a network structure wherein the polymer composition has shape-memory behavior and can be formed into a permanent primary shape, re-formed into a stable secondary shape, and controllably actuated to recover the permanent primary shape. Polymers have optimal aliphatic network structures due to minimization of dangling chains by using monomers that are symmetrical and that have matching amine and hydroxyl groups providing polymers and polymer foams with clarity, tight (narrow temperature range) single transitions, and high shape recovery and recovery force that are especially useful for implanting in the human body.