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Sample records for azobenzene nanoparticle-embedded polyacrylic

  1. Nanoparticle embedded enzymes for improved lateral flow sensors

    DEFF Research Database (Denmark)

    Özalp, Veli Cengiz; Zeydanlı, Uğur S.; Lunding, Anita;

    2013-01-01

    In this study, combining the nanoparticle embedded sensors with lateral flow assays, a novel strategy for ensuring the quality of signalling in lateral flow assays (LFAs) was developed. A LFA for reactive oxygen species (ROS) is reported that is based on horse radish peroxidase (HRP) which is co...... hydrogen peroxides was quantified with this novel LFA-ROS sensor to obtain a linear range between 1 and 25 μM. Nanoparticle embedding of enzymes is proposed here as a general strategy for developing enzyme-based lateral flow assays, eliminating adverse effects associated with biological samples....

  2. Azobenzene-functionalized cascade molecules

    DEFF Research Database (Denmark)

    Archut, A.; Vogtle, F.; De Cola, L.;

    1998-01-01

    Cascade molecules bearing up to 32 azobenzene groups in the periphery have been prepared from poly(propylene imine) dendrimers and N-hydroxysuccinimide esters. The dendritic azobenzene species show similar isomerization properties as the corresponding azobenzene monomers. The all-E azobenzene den...

  3. Strain Distribution of Au and Ag Nanoparticles Embedded in Al2O3 Thin Film

    Directory of Open Access Journals (Sweden)

    Honghua Huang

    2014-01-01

    Full Text Available Au and Ag nanoparticles embedded in amorphous Al2O3 matrix are fabricated by the pulsed laser deposition (PLD method and rapid thermal annealing (RTA technique, which are confirmed by the experimental high-resolution transmission electron microscope (HRTEM results, respectively. The strain distribution of Au and Ag nanoparticles embedded in the Al2O3 matrix is investigated by the finite-element (FE calculations. The simulation results clearly indicate that both the Au and Ag nanoparticles incur compressive strain by the Al2O3 matrix. However, the compressive strain existing on the Au nanoparticle is much weaker than that on the Ag nanoparticle. This phenomenon can be attributed to the reason that Young’s modulus of Au is larger than that of Ag. This different strain distribution of Au and Ag nanoparticles in the same host matrix may have a significant influence on the technological potential applications of the Au-Ag alloy nanoparticles.

  4. Microwave absorber based on silver nanoparticle-embedded polymer thin film.

    Science.gov (United States)

    Ramesh, G V; Sudheendran, K; Raju, K C James; Sreedhar, B; Radhakrishnan, T P

    2009-01-01

    Silver nanoparticle-embedded poly(vinyl alcohol) films are fabricated through a simple in situ process. The nanocomposite films are a few hundred nanometers thick with silver concentrations below 10% and the nanoparticles 5-10 nm in diameter. These films are shown to exhibit appreciable microwave absorption in the 8-12 GHz range; the return and insertion losses are found to be sensitive to the nanoparticle content. PMID:19441305

  5. Annealing effect on the ultrafast dynamics of Ag nanoparticles embedded in soda-lime silicate glasses

    International Nuclear Information System (INIS)

    Ag nanoparticles embedded in soda-lime silicate glasses were fabricated by the ion-exchange technique. Effects of thermal treatment on the optical nonlinearity and ultrafast dynamics of Ag nanoparticles were investigated by applying time-resolved optical Kerr effect and pump-probe techniques. The results indicate that thermal treatment is an efficient method to improve the nonlinear optical performance of this kind of material.

  6. Surface Wave Velocity of Crosslinked Polyacrylate Gels

    Science.gov (United States)

    Matsuoka, Tatsuro; Kinouchi, Wataru; ShinobuKoda, ShinobuKoda; Nomura, Hiroyasu

    1999-05-01

    Surface wave velocities of crosslinked polyacrylate hydrogelswere measured as a function of water content with differentcompositions of sodium polyacrylate (NaPA) and polyacrylic acid (PAA).The water content and composition dependencies of the surface wavevelocity were discussed.

  7. Irradiation of polyacrylate compositions in air

    International Nuclear Information System (INIS)

    The invention relates to processes for polymerizing polyacrylate functional compositions and in particular to processes for the curing in air of certain polyacrylate functional materials by irradiation

  8. Enhanced antioxidant activity of gold nanoparticle embedded 3,6-dihydroxyflavone: a combinational study

    Science.gov (United States)

    Medhe, Sharad; Bansal, Prachi; Srivastava, Man Mohan

    2012-12-01

    The antioxidative effect of selected dietary compounds (3,6-dihydroxyflavone, lutein and selenium methyl selenocysteine) was determined in single and combination using DPPH (2,2-diphenyl-l-picrylhydrazyl), OH (hydroxyl), H2O2 (hydrogen peroxide) and NO (nitric oxide) radical scavenging assays. Radical scavenging effect of the dietary phytochemicals individually are found to be in the order: ascorbic acid (standard) > lutein > 3,6-dihydroxyflavone > selenium methyl selenocysteine, at concentration 100 μg/ml, confirmed by all the four bioassays (p nanotech enforcement of dietary phytochemicals shows the utility in the architecture of nanoparticle embedded phytoproducts having a wide range of applications in medical science.

  9. Magnetoacoustic imaging of magnetic iron oxide nanoparticles embedded in biological tissues with microsecond magnetic stimulation

    Science.gov (United States)

    Hu, Gang; He, Bin

    2012-01-01

    We present an experimental study on magnetoacoustic imaging of superparamagnetic iron oxide (SPIO) nanoparticles embedded in biological tissues. In experiments, a large-current-carrying coil is used to deliver microsecond pulsed magnetic stimulation to samples. The ultrasound signals induced by magnetic forces on SPIO nanoparticles are measured by a rotating transducer. The distribution of nanoparticles is reconstructed by a back-projection imaging algorithm. The results demonstrated the feasibility to obtain cross-sectional image of magnetic nanoparticle targets with faithful dimensional and positional information, which suggests a promising tool for tomographic reconstruction of magnetic nanoparticle-labeled diseased tissues (e.g., cancerous tumor) in molecular or clinic imaging.

  10. Ultrafast dynamics of copper nanoparticles embedded in soda-lime silicate glass fabricated by ion exchange

    International Nuclear Information System (INIS)

    Copper nanoparticles embedded in soda-lime glass were fabricated by ion exchange followed by thermal treatment in hydrogen. The ultrafast dynamics of the embedded Cu nanoparticles formed under different fabrication conditions were investigated by applying femtosecond pump-probe technique. Non-Fermi electrons were suggested to be dominant in the transient behavior of the nanocomposites far from surface plasmon resonance of Cu. The long ion-exchange processing time was found to benefit and improve the ultrafast response of the fabricated nanocomposites.

  11. Tunneling Anisotropic Magnetoresistance in Fe Nanoparticles Embedded in MgO Matrix

    Science.gov (United States)

    Pham, T. V.; Miwa, S.; Suzuki, Y.

    2016-05-01

    The tunnel magnetoresistance (TMR) effect is related to the relative orientation of the magnetizations of the two ferromagnetic electrodes in magnetic tunnel junctions (MTJs). The tunnel anisotropic magnetoresistance (TAMR) effect is related to the orientation of the magnetization with respect to the current direction or the crystallographic axes. Beyond the TMR, the TAMR is not only present in MTJs in which both electrodes are ferromagnetic but may also appear in tunnel structures with a single magnetic electrode. We investigated the magnetotransport properties in an Au/MgO/Fe nanoparticles/MgO/Cu tunnel junction. We found that both the TMR and TAMR can appear in tunnel junctions with Fe nanoparticles embedded in an MgO matrix. The TMR is attributed to spin-dependent tunneling between Fe nanoparticles, so the device resistance depends on the magnetization directions of adjacent Fe nanoparticles. The TAMR is attributed to the interfacial spin-orbit interaction, so the device resistance depends on each magnetization direction of an Fe nanoparticle. This is the first observation of the TAMR in Fe nanoparticles embedded in an MgO matrix.

  12. Silver nanoparticle-embedded polymersome nanocarriers for the treatment of antibiotic-resistant infections

    Science.gov (United States)

    Geilich, Benjamin M.; van de Ven, Anne L.; Singleton, Gloria L.; Sepúlveda, Liuda J.; Sridhar, Srinivas; Webster, Thomas J.

    2015-02-01

    The rapidly diminishing number of effective antibiotics that can be used to treat infectious diseases and associated complications in a physician's arsenal is having a drastic impact on human health today. This study explored the development and optimization of a polymersome nanocarrier formed from a biodegradable diblock copolymer to overcome bacterial antibiotic resistance. Here, polymersomes were synthesized containing silver nanoparticles embedded in the hydrophobic compartment, and ampicillin in the hydrophilic compartment. Results showed for the first time that these silver nanoparticle-embedded polymersomes (AgPs) inhibited the growth of Escherichia coli transformed with a gene for ampicillin resistance (bla) in a dose-dependent fashion. Free ampicillin, AgPs without ampicillin, and ampicillin polymersomes without silver nanoparticles had no effect on bacterial growth. The relationship between the silver nanoparticles and ampicillin was determined to be synergistic and produced complete growth inhibition at a silver-to-ampicillin ratio of 1 : 0.64. In this manner, this study introduces a novel nanomaterial that can effectively treat problematic, antibiotic-resistant infections in an improved capacity which should be further examined for a wide range of medical applications.

  13. Gold nanoparticles embedded in organic/inorganic hybrid matrix: electrical and electrochemical behavior (withdrawal notice)

    Science.gov (United States)

    Moreira, Sandra D. F. C.; Silva, J. P. B.; Silva, Carlos J. R.; Capan, I.; Gomes, M. J. M.; Costa, Manuel F. M.

    2013-05-01

    Gold nanoparticles (AuNPs) with different diameters, from 3 to 32 nm, were immobilized in amine-alcohol-silicate matrix by mixing a preformed nanoparticle colloid with the precursors of amine-alcohol-silicate (AAs) prior to the solgel transition. These nanocomposites show high optical quality and optical features dictated by the size of the nanoparticle dopants but also present a high degree of flexibility which can largely enhance the range of practical applications. The current-voltage, impedance and capacitance-voltage characteristics of these materials have been measured. The electrochemical and impedimetric results reveal that AuNPs with different sizes give different signals, thus providing useful information that allows the employment of AuNPs in electrochemical biosensors. Capacitance- voltage measurements showed that these composites embedded AuNPs exhibited a large hysteresis window of 2.4V which indicates the possibility of charge storage in the Au nanoparticles embedded AAs hybrids.

  14. Noble metal nanoparticles embedding into polymeric materials: From fundamentals to applications.

    Science.gov (United States)

    Prakash, Jai; Pivin, J C; Swart, H C

    2015-12-01

    This review covers some key concepts related to embedding of the noble metal nanoparticles in polymer surfaces. The metal nanoparticles embedded into the polymer matrix can provide high-performance novel materials that find applications in modern nanotechnology. In particular, the origin of various processes that drive the embedding phenomenon, growth of the nanostructure at the surface, factors affecting the embedding including role of surface, interface energies and thermodynamic driving forces with emphasis on the fundamental and technological applications, under different conditions (annealing and ion beams) have been discussed. In addition to the conventional thermal process for embedding which includes the measure of fundamental polymer surface properties with relevant probing techniques, this review discusses the recent advances carried out in the understanding of embedding phenomenon starting from thin metal films to growth of the nanoparticles and embedded nanostructures using novel ion beam techniques. PMID:26584861

  15. Cobalt nanoparticles-embedded magnetic ordered mesoporous carbon for highly effective adsorption of rhodamine B

    International Nuclear Information System (INIS)

    Highlights: • Cobalt nanoparticles-embedded magnetic ordered mesoporous carbon (Co/OMC) was applied as a novel adsorption material to remove rhodamine B. • Co/OMC was synthesized by directly introducing cobalt into OMC through a simple infusing method. • High removal capacity of rhodamine B: maximum adsorption capacity reaches 468 mg/g at 200 mg/L initial rhodamine B concentration. • Very quick adsorption property: 96% of rhodamine B can be removed within 25 min. - Abstract: Cobalt nanoparticles-embedded magnetic ordered mesoporous carbon (Co/OMC), prepared through a simple method involving infusing and calcination, was used as a highly effective adsorbent for rhodamine B (Rh B) removal. Several techniques, including SEM, HRTEM, nitrogen adsorption–desorption isotherms, XRD, Raman spectra, EDX, zeta potential and VSM measurement, were applied to characterize the adsorbent. Batch tests were conducted to investigate the adsorption performance. The adsorption capacity of the resultant adsorbent was relatively high compared with raw ordered mesoporous carbon (OMC) and reached an equilibrium value of 468 mg/g at 200 mg/L initial Rh B concentration. Removal efficiency even reached 96% within 25 min at 100 mg/L initial Rh B concentration. Besides, the adsorption amount increased with the increase of solution pH, adsorbent dose and initial Rh B concentration. Kinetics study showed that the adsorption agreed well with pseudo-second-order model (R2 = 0.999) and had a significant correlation with intra-particle diffusion model in the both two adsorption periods. Furthermore, thermodynamics research indicated that the adsorption process was endothermic and spontaneous in nature. The adsorption isotherms fitted well with Langmuir model, demonstrating the formation of mono-molecular layer on the surface of Co/OMC during adsorption process. The results confirmed that Co/OMC has the potential superiority in removal of Rh B from aqueous solution

  16. Melting and Solidification Behaviour of Bi-Pb Multiphase Alloy Nanoparticles Embedded in Aluminum Matrix.

    Science.gov (United States)

    Khan, Patan Yousaf; Biswas, Krishanu

    2015-01-01

    The present investigation reports the result of the investigation on the phase transformation of biphasic Bi-Pb alloy nanoparticles embedded in the aluminum matrix. The samples are prepared by rapid solidification route involving melt spinning of Al-6 wt% (Bi55.9Pb44.1) alloy on a rotating copper wheel in an argon-filled evacuated chamber. The detailed transmission electron microscope (TEM) investigation shows presence of near cuboctahedral shaped biphasic nano-inclusions consisting of the (Bi) solid solution and β, the intermediate phase. β constitutes bulk of the nanoparticle with (Bi) forming the cap. Both the phases bear distinct orientation relationship with the matrix. The compositional analysis indicates substantial increase in solid solubilities of Pb in the (Bi) and Bi in the β-phases as compared to the as-cast sample. Differential scanning calorimetric (DSC) studies indicate substantial superheating (16.4 K) of the embedded nanoparticles with appearance of sharp melting peak. The solidification is observed to be diffused, taking place over a large temperature range (344.5 K to 332 K). The in situ heating stage experiments carried out in TEM indicate formation of core shell morphology during heating with β forming the shell around (Bi). The melting starts from Al/β/(Bi) triple point and then the liquid spreads along matrix-particle interface. The solidification occurs in eutectic manner. PMID:26328350

  17. Magnetic properties of Ni nanoparticles embedded in silica matrix (KIT-6) synthesized via novel chemical route

    Energy Technology Data Exchange (ETDEWEB)

    Dalavi, Shankar B.; Panda, Rabi N., E-mail: rnp@goa.bits-pilani.ac.in [Department of Chemistry, BITS-Pilani, K. K. Birla Goa Campus, Zuarinagar, Goa-403726 (India); Raja, M. Manivel [Defence Metallurgical Research Laboratory, Hyderabad-500058 (India)

    2015-06-24

    Thermally stable Ni nanoparticles have been embedded in mesoporous silica matrix (KIT-6) via novel chemical reduction method by using superhydride as reducing agent. X-ray diffraction (XRD) study confirms that pure and embedded Ni nanoparticles crystallize in face centered cubic (fcc) structure. Crystallite sizes of pure Ni, 4 wt% and 8 wt% Ni in silica were estimated to be 6.0 nm, 10.4 nm and 10.5 nm, respectively. Morphology and dispersion of Ni in silica matrix were studied by scanning electron microscopy (SEM). Magnetic study shows enhancement of magnetic moments of Ni nanoparticles embedded in silica matrix compared with that of pure Ni. The result has been interpreted on the basis of size reduction and magnetic exchange effects. Saturation magnetization values for pure Ni, 4 wt% and 8 wt% Ni in silica were found to be 15.77 emu/g, 5.08 emu/g and 2.00 emu/g whereas coercivity values were 33.72 Oe, 92.47 Oe and 64.70 Oe, respectively. We anticipate that the observed magnetic properties may find application as soft magnetic materials.

  18. Transport properties of β-Ga2O3 nanoparticles embedded in Nb thin films

    Directory of Open Access Journals (Sweden)

    L.S. Vaidhyanathan

    2015-01-01

    Full Text Available The origin of ferromagnetism in nanoparticles of nonmagnetic oxides is an interesting area of research. In the present work, transport properties of niobium thin films, with β-Ga2O3 nanoparticles embedded within them, are presented. Nanoparticles of β-Ga2O3 embedded in a Nb matrix were prepared at room temperature by radio frequency co-sputtering technique on Si (100 and glass substrates held at room temperature. The thin films deposited on Si substrates were subjected to Ar annealing at a temperature range of 600-650 C for 1 hour. Films were characterized by X-ray diffraction (XRD, Micro-Raman and elemental identification was performed with an Energy Dispersive X-ray Spectroscopy (EDS. Transport measurements were performed down to liquid helium temperatures by four-probe contact technique, showed characteristics analogous to those observed in the context of a Kondo system. A comparison of the experimental data with the theoretical formalism of Kondo and Hamann is presented. It is suggested that this behavior arises from the existence of magnetic moments associated with the oxygen vacancy defects in the nanoparticles of the nonmagnetic oxide Ga2O3.

  19. FMR study of magnetic nanoparticles embedded in non-magnetic matrix

    Directory of Open Access Journals (Sweden)

    N. Guskos

    2007-09-01

    Full Text Available Purpose: The aim of this review is recapitulating the FMR study of low concentration of magnetic nanoparticles in non-magnetic matrices.Design/methodology/approach: Magnetic nanoparticles exhibit a variety of anomalous magnetic properties and they could be used for forming low concentration in different matrices. This way, they are being found to be allowing for effectively novel applications of FMR (ferromagnetic resonance for easier trustworthy characterisation of a variety of materials. α-Fe, Co, Fe3C, γ- Fe2O3, Fe3O4 magnetic nanoparticles have been used as low concentration fillers in paraffin, concrete, resin and polymers/copolymers.Findings: For all these matrices, the intensities of the FMR spectra are recorded decreasing with temperature lowering in the high temperature region, whilst the resonance locus is shifted to the direction of lower magnetic field, essentially changing the resonance condition. These parameters of the FMR spectra are seen depending upon kind of nanoparticle host in such a way that this method could be useful for studying dynamical processes of the matrices. Interestingly enough, a very low concentration of magnetic nanoparticles embedded in the non-magnetic matrix could modify its glass-state emanation or melting transition.Research limitations/implications: Composite systems containing magnetic nanoparticles promise the potential for high-density data storage, biomedical applications, catalysis, and nanotechnology sensor materialisation, among other envisaged utilisations.Originality/value: Continue attempting to decipher the mystery and fruitfulness of magnetic nanoparticle distributions.

  20. Polymeric nanoparticles-embedded organogel for roxithromycin delivery to hair follicles.

    Science.gov (United States)

    Główka, Eliza; Wosicka-Frąckowiak, Hanna; Hyla, Kinga; Stefanowska, Justyna; Jastrzębska, Katarzyna; Klapiszewski, Łukasz; Jesionowski, Teofil; Cal, Krzysztof

    2014-09-01

    Drug delivery into hair follicles with the use of nanoparticles (NPs) is gaining more importance as drug-loaded NPs may accumulate in hair follicle openings. The aim was to develop and evaluate a pluronic lecithin organogel (PLO) with roxithromycin (ROX)-loaded NPs for follicular targeting. Polymeric NPs were evaluated in terms of particle shape, size, zeta potential, suspension stability, encapsulation efficiency and in vitro drug release. Lyophilized NPs were incorporated into the PLO and rheological measurements of the nanoparticles-embedded organogels were done. The fate of the NPs in the skin was traced by incorporation of a fluorescent dye into the NPs. As a result, ROX was efficiently incorporated into polymeric NPs characterized by the appropriate size (approximately 300 nm) allowing drug delivery to hair follicles. In ex vivo human skin penetration studies, horizontal skin sections revealed fluorescence deep in the hair follicles. Although the organogel has higher affinity to the lipidic follicular area than an aqueous suspension of NPs, it did not seem to improve penetration of the NPs along the hair shaft. The results proved that it was possible to achieve preferential targeting to the pilosebaceous unit using polymeric NPs formulated either into the aqueous suspension or semisolid topical formulation. PMID:25014763

  1. Magnetic properties of Ni nanoparticles embedded in silica matrix (KIT-6) synthesized via novel chemical route

    International Nuclear Information System (INIS)

    Thermally stable Ni nanoparticles have been embedded in mesoporous silica matrix (KIT-6) via novel chemical reduction method by using superhydride as reducing agent. X-ray diffraction (XRD) study confirms that pure and embedded Ni nanoparticles crystallize in face centered cubic (fcc) structure. Crystallite sizes of pure Ni, 4 wt% and 8 wt% Ni in silica were estimated to be 6.0 nm, 10.4 nm and 10.5 nm, respectively. Morphology and dispersion of Ni in silica matrix were studied by scanning electron microscopy (SEM). Magnetic study shows enhancement of magnetic moments of Ni nanoparticles embedded in silica matrix compared with that of pure Ni. The result has been interpreted on the basis of size reduction and magnetic exchange effects. Saturation magnetization values for pure Ni, 4 wt% and 8 wt% Ni in silica were found to be 15.77 emu/g, 5.08 emu/g and 2.00 emu/g whereas coercivity values were 33.72 Oe, 92.47 Oe and 64.70 Oe, respectively. We anticipate that the observed magnetic properties may find application as soft magnetic materials

  2. Unusual photoanisotropic alignment in amorphous azobenzene polymers

    DEFF Research Database (Denmark)

    Ramanujam, P.S.

    2015-01-01

    560 and 630nm, where the absorption is minimal, results in a possible uniaxial hedgehog arrangement of the molecules. Experiments performed with a dye laser, which can be tuned continuously between 560 and 630nm, are described. Not only azobenzene but also another photosensitive molecule...

  3. Photoinduced Deformation of Azobenzene Polyester Films

    DEFF Research Database (Denmark)

    Bublitz, D.; Helgert, M.; Fleck, B.;

    2000-01-01

    We investigate two types of azobenzene side-chain polyesters which have shown opposite behaviour in light-induced surface grating formation experiments. Thin films of these polymers prepared on a water surface undergo opposite changes of shape under the influence of polarized light. We propose this...

  4. Subsurface synthesis and characterization of Ag nanoparticles embedded in MgO

    International Nuclear Information System (INIS)

    Metal nanoparticles exhibit a localized surface plasmon resonance (LSPR) which is very sensitive to the size and shape of the nanoparticle and the surrounding dielectric medium. The coupling between the electromagnetic radiation and the localized surface plasmon in metallic nanoparticles results in a sizable enhancement of the incident fields, making them possible candidates for plasmonic applications. In particular, partially exposed metallic nanoparticles distributed in a dielectric matrix can provide prime locations for LSPR spectroscopy and sensing. We report the synthesis and characterization of a plasmonic substrate consisting of Ag nanoparticles partially buried in MgO. Ag nanoparticles of different shapes and size distributions were synthesized below the surface of MgO by implanting 200 keV Ag+ ions followed by annealing at 1000 °C for 10 and 30 h. A detailed optical and structural characterization was carried out to understand the evolution of the Ag nanoparticle and size distribution inside the MgO matrix. Micro x-ray diffraction (Micro-XRD) was employed to investigate the structural properties and estimate the crystallite size. The nanoparticles evolved from a spherical to a faceted morphology with annealing time, assuming an octahedral shape truncated at the (001) planes, as visualized from aberration-corrected transmission electron microscopy (TEM) images. The nanoparticles embedded in MgO were shown to be pure metallic Ag using atom probe tomography (APT). The nanoparticles were partially exposed to the surface by employing plasma etch techniques to remove the overlaying MgO. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were employed to study the surface morphology and obtain a height distribution for the partially exposed nanoparticles. (paper)

  5. Subsurface synthesis and characterization of Ag nanoparticles embedded in MgO

    Science.gov (United States)

    Vilayurganapathy, S.; Devaraj, A.; Colby, R.; Pandey, A.; Varga, T.; Shutthanandan, V.; Manandhar, S.; El-Khoury, P. Z.; Kayani, Asghar; Hess, W. P.; Thevuthasan, S.

    2013-03-01

    Metal nanoparticles exhibit a localized surface plasmon resonance (LSPR) which is very sensitive to the size and shape of the nanoparticle and the surrounding dielectric medium. The coupling between the electromagnetic radiation and the localized surface plasmon in metallic nanoparticles results in a sizable enhancement of the incident fields, making them possible candidates for plasmonic applications. In particular, partially exposed metallic nanoparticles distributed in a dielectric matrix can provide prime locations for LSPR spectroscopy and sensing. We report the synthesis and characterization of a plasmonic substrate consisting of Ag nanoparticles partially buried in MgO. Ag nanoparticles of different shapes and size distributions were synthesized below the surface of MgO by implanting 200 keV Ag+ ions followed by annealing at 1000 °C for 10 and 30 h. A detailed optical and structural characterization was carried out to understand the evolution of the Ag nanoparticle and size distribution inside the MgO matrix. Micro x-ray diffraction (Micro-XRD) was employed to investigate the structural properties and estimate the crystallite size. The nanoparticles evolved from a spherical to a faceted morphology with annealing time, assuming an octahedral shape truncated at the (001) planes, as visualized from aberration-corrected transmission electron microscopy (TEM) images. The nanoparticles embedded in MgO were shown to be pure metallic Ag using atom probe tomography (APT). The nanoparticles were partially exposed to the surface by employing plasma etch techniques to remove the overlaying MgO. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were employed to study the surface morphology and obtain a height distribution for the partially exposed nanoparticles.

  6. Oxidation behavior of Cu nanoparticles embedded into semiconductive TiO{sub 2} matrix

    Energy Technology Data Exchange (ETDEWEB)

    Stranak, Vitezslav, E-mail: stranak@prf.jcu.cz [University of South Bohemia, Faculty of Science, Branisovska 31, 37005 Ceske Budejovice (Czech Republic); Drache, Steffen; Wulff, Harm [University of Greifswald, Institute of Physics, Felix-Hausdorff-Str. 6, 17489 Greifswald (Germany); Hubicka, Zdenek [Institute of Physics, Academy of Science of the Czech Republic, Na Slovance 2, 18221 Prague (Czech Republic); Tichy, Milan [Charles University in Prague, Faculty of Mathematics and Physics, V Holesovickach 2, 18000 Prague (Czech Republic); Kruth, Angela [Leibniz Institute for Plasma Science and Technology, INP Greifswald e.V., Felix-Hausdorff-Straße 2, 17489 Greifswald (Germany); Helm, Christiane A.; Hippler, Rainer [University of Greifswald, Institute of Physics, Felix-Hausdorff-Str. 6, 17489 Greifswald (Germany)

    2015-08-31

    Metal nanoparticles embedded into a semiconductive matrix represent a promising material for widely sought advanced technological applications. We focused our interest on the preparation of TiO{sub 2} matrix with embedded Cu nanoparticles. In particular, we studied the effect of reactive discharge (Ar/O{sub 2}) exposition on copper oxidation, which can result in two stable forms: cuprous oxide (Cu{sub 2}O) and cupric oxide (CuO). Copper nanoparticles, of size in range 10–50 nm, were produced by magnetron sputtering in combination with gas aggregation. The beam of Cu nanoparticles was impinging onto a silicon substrate which was directly exposed to a reactive Ar/O{sub 2} magnetron discharge providing sputtering of Ti target at the same time. The properties of deposited nanocomposite Cu({sub x}O)–TiO{sub 2} were investigated by X-ray photoelectron spectroscopy, grazing incidence X-ray diffractometry, X-ray reflectometry and scanning electron microscopy techniques to reveal the nanocomposite properties and to understand the oxidation process of embedded Cu nanoparticles. It was found that CuO is preferentially formed if copper is exposed to active oxygen species (O{sup +}, O{sup −}, O{sup ⁎} etc.) produced in the reactive magnetron discharge. On the other hand, Cu{sub 2}O was observed in the case of copper reaction in ambient Ar/O{sub 2} atmosphere. As a result, two possible copper oxidation mechanisms are proposed, employing chemical kinetics. - Highlights: • Cu–TiO{sub 2} nanocomposite was prepared by plasma assisted methods. • Embedded Cu always occurs in oxidized phase depending on the way of oxidation. • CuO is formed if copper is exposed to active oxygen species produced in Ar/O{sub 2} discharge. • Cu{sub 2}O appears in the case of copper reaction in an ambient oxygen-based atmosphere. • Two possible copper oxidation mechanisms are proposed.

  7. Subsurface synthesis and characterization of Ag nanoparticles embedded in MgO.

    Science.gov (United States)

    Vilayurganapathy, S; Devaraj, A; Colby, R; Pandey, A; Varga, T; Shutthanandan, V; Manandhar, S; El-Khoury, P Z; Kayani, Asghar; Hess, W P; Thevuthasan, S

    2013-03-01

    Metal nanoparticles exhibit a localized surface plasmon resonance (LSPR) which is very sensitive to the size and shape of the nanoparticle and the surrounding dielectric medium. The coupling between the electromagnetic radiation and the localized surface plasmon in metallic nanoparticles results in a sizable enhancement of the incident fields, making them possible candidates for plasmonic applications. In particular, partially exposed metallic nanoparticles distributed in a dielectric matrix can provide prime locations for LSPR spectroscopy and sensing. We report the synthesis and characterization of a plasmonic substrate consisting of Ag nanoparticles partially buried in MgO. Ag nanoparticles of different shapes and size distributions were synthesized below the surface of MgO by implanting 200 keV Ag(+) ions followed by annealing at 1000 °C for 10 and 30 h. A detailed optical and structural characterization was carried out to understand the evolution of the Ag nanoparticle and size distribution inside the MgO matrix. Micro x-ray diffraction (Micro-XRD) was employed to investigate the structural properties and estimate the crystallite size. The nanoparticles evolved from a spherical to a faceted morphology with annealing time, assuming an octahedral shape truncated at the (001) planes, as visualized from aberration-corrected transmission electron microscopy (TEM) images. The nanoparticles embedded in MgO were shown to be pure metallic Ag using atom probe tomography (APT). The nanoparticles were partially exposed to the surface by employing plasma etch techniques to remove the overlaying MgO. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were employed to study the surface morphology and obtain a height distribution for the partially exposed nanoparticles. PMID:23403363

  8. Hydrothermal Synthesis and Processing of Barium Titanate Nanoparticles Embedded in Polymer Films.

    Science.gov (United States)

    Toomey, Michael D; Gao, Kai; Mendis, Gamini P; Slamovich, Elliott B; Howarter, John A

    2015-12-30

    Barium titanate nanoparticles embedded in flexible polymer films were synthesized using hydrothermal processing methods. The resulting films were characterized with respect to material composition, size distribution of nanoparticles, and spatial location of particles within the polymer film. Synthesis conditions were varied based on the mechanical properties of the polymer films, ratio of polymer to barium titanate precursors, and length of aging time between initial formulations of the solution to final processing of nanoparticles. Block copolymers of poly(styrene-co-maleic anhydride) (SMAh) were used to spatially separate titanium precursors based on specific chemical interactions with the maleic anhydride moiety. However, the glassy nature of this copolymer restricted mobility of the titanium precursors during hydrothermal processing. The addition of rubbery butadiene moieties, through mixing of the SMAh with poly(styrene-butadiene-styrene) (SBS) copolymer, increased the nanoparticle dispersion as a result of greater diffusivity of the titanium precursor via higher mobility of the polymer matrix. Additionally, an aminosilane was used as a means to retard cross-linking in polymer-metalorganic solutions, as the titanium precursor molecules were shown to react and form networks prior to hydrothermal processing. By adding small amounts of competing aminosilane, excessive cross-linking was prevented without significantly impacting the quality and composition of the final barium titanate nanoparticles. X-ray diffraction and X-ray photoelectron spectroscopy were used to verify nanoparticle compositions. Particle sizes within the polymer films were measured to be 108 ± 5 nm, 100 ± 6 nm, and 60 ± 5 nm under different synthetic conditions using electron microscopy. Flexibility of the films was assessed through measurement of the glass transition temperature using dynamic mechanical analysis. Dielectric permittivity was measured using an impedance analyzer. PMID

  9. Oxidation behavior of Cu nanoparticles embedded into semiconductive TiO2 matrix

    International Nuclear Information System (INIS)

    Metal nanoparticles embedded into a semiconductive matrix represent a promising material for widely sought advanced technological applications. We focused our interest on the preparation of TiO2 matrix with embedded Cu nanoparticles. In particular, we studied the effect of reactive discharge (Ar/O2) exposition on copper oxidation, which can result in two stable forms: cuprous oxide (Cu2O) and cupric oxide (CuO). Copper nanoparticles, of size in range 10–50 nm, were produced by magnetron sputtering in combination with gas aggregation. The beam of Cu nanoparticles was impinging onto a silicon substrate which was directly exposed to a reactive Ar/O2 magnetron discharge providing sputtering of Ti target at the same time. The properties of deposited nanocomposite Cu(xO)–TiO2 were investigated by X-ray photoelectron spectroscopy, grazing incidence X-ray diffractometry, X-ray reflectometry and scanning electron microscopy techniques to reveal the nanocomposite properties and to understand the oxidation process of embedded Cu nanoparticles. It was found that CuO is preferentially formed if copper is exposed to active oxygen species (O+, O−, O⁎ etc.) produced in the reactive magnetron discharge. On the other hand, Cu2O was observed in the case of copper reaction in ambient Ar/O2 atmosphere. As a result, two possible copper oxidation mechanisms are proposed, employing chemical kinetics. - Highlights: • Cu–TiO2 nanocomposite was prepared by plasma assisted methods. • Embedded Cu always occurs in oxidized phase depending on the way of oxidation. • CuO is formed if copper is exposed to active oxygen species produced in Ar/O2 discharge. • Cu2O appears in the case of copper reaction in an ambient oxygen-based atmosphere. • Two possible copper oxidation mechanisms are proposed

  10. Silver nanoparticles embedded polymer sorbent for preconcentration of uranium from bio-aggressive aqueous media

    Energy Technology Data Exchange (ETDEWEB)

    Das, Sadananda [Department of Chemistry, University of Pune, Pune 411 007 (India); Radiochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Pandey, Ashok K., E-mail: ashokk@barc.gov.in [Radiochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Athawale, Anjali A. [Department of Chemistry, University of Pune, Pune 411 007 (India); Subramanian, M. [Bio-organic Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Seshagiri, T.K. [Radiochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Khanna, Pawan K. [Nanoscience Laboratory, Centre for Materials for Electronics Technology, Pune 411 008 (India); Manchanda, Vijay K. [Radiochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India)

    2011-02-28

    Adsorptive sorbent for bio-aggressive natural aqueous media like seawater was developed by one pot simultaneous synthesis of silver nanoparticles (Ag nps) and poly(ethylene glycol methacrylate phosphate) (PEGMP) by UV-initiator induced photo-polymerization. The photo-polymerization was carried out by irradiating N,N'-dimethylformamide (DMF) solution containing appropriate amounts of the functional monomer (ethylene glycol methacrylate phosphate), UV initiator ({alpha},{alpha}'-dimethoxy-{alpha}-phenyl acetophenone), and Ag{sup +} ions with 365 nm UV light in a multilamps photoreactor. To increase mechanical strength, nano-composite sorbent (Ag-PEGMP) was also reinforced with thermally bonded non-woven poly(propylene) fibrous sheet. Transmission electron microscopy (TEM) of the nano-composite sorbent showed uniform distribution of spherical Ag nanoparticles with particles size ranging from 3 to 6 nm. The maximum amount of Ag{sup 0} that could be anchored in the form of nanoparticles were 5 {+-} 1 and 10 {+-} 1 wt.% in self-supported PEGMP and poly(propylene) reinforced PEGMP matrices, respectively. Ag-PEGMP sorbent was found to be stable under ambient conditions for a period of six months. Ag-PEGMP composite sorbent did not exhibit growth at all after incubation with pre-grown Escherichia coli cells, and showed non-adherence of this bacteria to the composite. This indicated that composite sorbent has the bio-resistivity due to bacterial repulsion and bactericidal properties of Ag nanoparticles embedded in the PEGMP. Sorption of U(VI) in PEGMP and Ag-PEGMP nano-composite sorbents from well-stirred seawater was studied to explore the possibility of using it for uranium preconcentration from bio-aggressive aqueous streams. The nano-composite sorbent was used to preconcentrate U(VI) from a process aqueous waste stream.

  11. Graphene oxide catalyzed cis-trans isomerization of azobenzene

    Directory of Open Access Journals (Sweden)

    Dongha Shin

    2014-09-01

    Full Text Available We report the fast cis-trans isomerization of an amine-substituted azobenzene catalyzed by graphene oxide (GO, where the amine functionality facilitates the charge transfer from azobenzene to graphene oxide in contrast to non-substituted azobenzene. This catalytic effect was not observed in stilbene analogues, which strongly supports the existence of different isomerization pathways between azobenzene and stilbene. The graphene oxide catalyzed isomerization is expected to be useful as a new photoisomerization based sensing platform complementary to GO-based fluorescence quenching methods.

  12. Deflocculation of clay suspensions using sodium polyacrylates

    Science.gov (United States)

    Jedlicka, P.

    1984-01-01

    Rheological properties of elutriated kaolin suspensions deflocculated by Na polyacrylate (DAC 3 and DAC 4) were studied and compared to those deflocculated by the conventional Na2CO3 water and glass and imported Dispex N40. The deflocculating effect of Na polyacrylate was comparable to that of Dispex N40. The optimum amounts of Na polyacrylate were determined for suspensions based on 5-type kaolin. The Na polyacrylate can be successfully used for decreasing the water content of ceramic slips for casting and spray drying.

  13. Thin films of metal-organic compounds and metal nanoparticle-embedded polymers for nonlinear optical applications

    Indian Academy of Sciences (India)

    S Philip Anthony; Shatabdi Porel; D Narayana Rao; T P Radhakrishnan

    2005-11-01

    Thin films based on two very different metal-organic systems are developed and some nonlinear optical applications are explored. A family of zinc complexes which form perfectly polar assemblies in their crystalline state are found to organize as uniaxially oriented crystallites in vapor deposited thin films on glass substrate. Optical second harmonic generation from these films is investigated. A simple protocol is developed for the in-situ fabrication of highly monodisperse silver nanoparticles in a polymer film matrix. The methodology can be used to produce free-standing films. Optical limiting capability of the nanoparticle-embedded polymer film is demonstrated.

  14. Phase decomposition of AuFe alloy nanoparticles embedded in silica matrix under swift heavy ion irradiation

    Science.gov (United States)

    Pannu, Compesh; Bala, Manju; Singh, U. B.; Srivastava, S. K.; Kabiraj, D.; Avasthi, D. K.

    2016-07-01

    AuFe alloy nanoparticles embedded in silica matrix are synthesized using atom beam sputtering technique and subsequently irradiated with 100 MeV Au ions at various fluences ranging from 1 × 1013 to 6 × 1013 ions/cm2. The X-ray diffraction, absorption spectroscopy, X-ray photo electron spectroscopy and transmission electron microscopy results show that swift heavy ion irradiation leads to decomposition of AuFe alloy nanoparticles from surface region and subsequent reprecipitation of Au and Fe nanoparticles occur. The process of phase decomposition and reprecipitation of individual element nanoparticles is explained on the basis of inelastic thermal spike model.

  15. Structure and magnetic properties of Fe nanoparticles embedded in a Cr matrix

    Energy Technology Data Exchange (ETDEWEB)

    Qureshi, M.T. [Department of Physics and Astronomy, University of Leicester, Leicester LE1 7RH (United Kingdom); Department of Physics, Hazara University, Mansehra (Pakistan); Baker, S.H. [Department of Physics and Astronomy, University of Leicester, Leicester LE1 7RH (United Kingdom); Binns, C., E-mail: cb12@le.ac.uk [Department of Physics and Astronomy, University of Leicester, Leicester LE1 7RH (United Kingdom); Roy, M. [Department of Physics and Astronomy, University of Leicester, Leicester LE1 7RH (United Kingdom); Laureti, S.; Fiorani, D.; Peddis, D. [ISM-CNR, Area della Ricerca, Via salaria Km 29,500, P.B. 10-00016, Monterotondo Scalo, Roma (Italy)

    2015-03-15

    The structure of 2 nm diameter (340 atoms) Fe nanoparticles embedded in a Cr matrix was determined using X-ray Absorption Fine Structure (EXAFS) and the magnetic properties studied by Superconducting Quantum Interference Device (SQUID) magnetometry. The thin films were produced by the co-deposition of pre-formed gas-phase Fe clusters synthesised by a gas aggregation source with an atomic vapour of Cr produced by an MBE source. The behaviour was studied as a function of Fe nanoparticle volume fraction in the range 5–20% and was compared to previous results on ferromagnetic nanoparticles in antiferromagnetic matrices. EXAFS showed that the atomic structure in the Cr-embedded Fe nanoparticles is the same as the bulk bcc structure. Whereas alloying between the nanoparticles and matrix material has previously been shown to be very pronounced for Co nanoparticles in antiferromagnetic Mn, it was found that any alloying between Fe nanoparticles and Cr matrix material is limited. For dilute samples of Fe nanoparticles in Cr the measured saturation magnetisation (M{sub S}) was 1µ{sub B}/Fe atom, which is significantly less than the bulk M{sub S} value of 2.22µ{sub B}/Fe atom indicating that the surface of Fe nanoparticles is either antiferromagnetic or non-magnetic. An increase in the volume fraction produces an increase in the value of M{sub S} and at a volume fraction of 20%, M{sub S} exceeds the value of bulk Fe showing that some Cr spins provide a ferromagnetic contribution. After field cooling below 30 K, all films show Exchange Bias (EB) and an increase of coercivity, which are both much larger for the most concentrated sample. The Cr spins at the surface of the Fe particles play a key role in determining the overall magnetic behaviour. - Highlights: • Fe nanoparticles in Cr matrices at low volume fraction have bcc structure. • Fe nanoparticles in Cr at low volume fraction have a magnetic moment of 1µB/atom. • At a volume fraction of 20% the interfacial Cr

  16. Photochromic liquid crystalline structures containing azobenzene moieties

    Czech Academy of Sciences Publication Activity Database

    Studenovský, Martin; Sedláková, Zdeňka; Wang, Geng; Nešpůrek, Stanislav; Janus, K.; Boiko, O. P.; Kajzar, F.

    2004-01-01

    Roč. 212, č. 1 (2004), s. 399-406. ISSN 1022-1360. [Electrical and Related Properties of Polymers and Other Organic Solids /9./. Prague, 14.07.2002-18.07.2002] R&D Projects: GA MŠk OC D14.30 Institutional research plan: CEZ:AV0Z4050913 Keywords : azobenzene * liquid crystal * photochromism Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 0.691, year: 2004

  17. DNA compaction by azobenzene-containing surfactant

    International Nuclear Information System (INIS)

    We report on the interaction of cationic azobenzene-containing surfactant with DNA investigated by absorption and fluorescence spectroscopy, dynamic light scattering, and atomic force microscopy. The properties of the surfactant can be controlled with light by reversible switching of the azobenzene unit, incorporated into the surfactant tail, between a hydrophobic trans (visible irradiation) and a hydrophilic cis (UV irradiation) configuration. The influence of the trans-cis isomerization of the azobenzene on the compaction process of DNA molecules and the role of both isomers in the formation and colloidal stability of DNA-surfactant complexes is discussed. It is shown that the trans isomer plays a major role in the DNA compaction process. The influence of the cis isomer on the DNA coil configuration is rather small. The construction of a phase diagram of the DNA concentration versus surfactant/DNA charge ratio allows distancing between three major phases: colloidally stable and unstable compacted globules, and extended coil conformation. There is a critical concentration of DNA above which the compacted globules can be hindered from aggregation and precipitation by adding an appropriate amount of the surfactant in the trans configuration. This is because of the compensation of hydrophobicity of the globules with an increasing amount of the surfactant. Below the critical DNA concentration, the compacted globules are colloidally stable and can be reversibly transferred with light to an extended coil state.

  18. DNA compaction by azobenzene-containing surfactant

    Science.gov (United States)

    Zakrevskyy, Yuriy; Kopyshev, Alexey; Lomadze, Nino; Morozova, Elena; Lysyakova, Ludmila; Kasyanenko, Nina; Santer, Svetlana

    2011-08-01

    We report on the interaction of cationic azobenzene-containing surfactant with DNA investigated by absorption and fluorescence spectroscopy, dynamic light scattering, and atomic force microscopy. The properties of the surfactant can be controlled with light by reversible switching of the azobenzene unit, incorporated into the surfactant tail, between a hydrophobic trans (visible irradiation) and a hydrophilic cis (UV irradiation) configuration. The influence of the trans-cis isomerization of the azobenzene on the compaction process of DNA molecules and the role of both isomers in the formation and colloidal stability of DNA-surfactant complexes is discussed. It is shown that the trans isomer plays a major role in the DNA compaction process. The influence of the cis isomer on the DNA coil configuration is rather small. The construction of a phase diagram of the DNA concentration versus surfactant/DNA charge ratio allows distancing between three major phases: colloidally stable and unstable compacted globules, and extended coil conformation. There is a critical concentration of DNA above which the compacted globules can be hindered from aggregation and precipitation by adding an appropriate amount of the surfactant in the trans configuration. This is because of the compensation of hydrophobicity of the globules with an increasing amount of the surfactant. Below the critical DNA concentration, the compacted globules are colloidally stable and can be reversibly transferred with light to an extended coil state.

  19. Cooperative Switching in Nanofibers of Azobenzene Oligomers.

    Science.gov (United States)

    Weber, Christopher; Liebig, Tobias; Gensler, Manuel; Zykov, Anton; Pithan, Linus; Rabe, Jürgen P; Hecht, Stefan; Bléger, David; Kowarik, Stefan

    2016-01-01

    Next-generation molecular devices and machines demand the integration of molecular switches into hierarchical assemblies to amplify the response of the system from the molecular level to the meso- or macro-scale. Here, we demonstrate that multi-azobenzene oligomers can assemble to form robust supramolecular nanofibers in which they can be switched repeatedly between the E- and Z-configuration. While in isolated oligomers the azobenzene units undergo reversible photoisomerization independently, in the nanofibers they are coupled via intermolecular interactions and switch cooperatively as evidenced by unusual thermal and kinetic behavior. We find that the photoisomerization rate from the Z-isomer to the E-isomer depends on the fraction of Z-azobenzene in the nanofibers, and is increased by more than a factor of 4 in Z-rich fibers when compared to E-rich fibers. This demonstrates the great potential of coupling individual photochromic units for increasing their quantum efficiency in the solid state with potential relevance for actuation and sensing. PMID:27161608

  20. Cooperative Switching in Nanofibers of Azobenzene Oligomers

    Science.gov (United States)

    Weber, Christopher; Liebig, Tobias; Gensler, Manuel; Zykov, Anton; Pithan, Linus; Rabe, Jürgen P.; Hecht, Stefan; Bléger, David; Kowarik, Stefan

    2016-01-01

    Next-generation molecular devices and machines demand the integration of molecular switches into hierarchical assemblies to amplify the response of the system from the molecular level to the meso- or macro-scale. Here, we demonstrate that multi-azobenzene oligomers can assemble to form robust supramolecular nanofibers in which they can be switched repeatedly between the E- and Z-configuration. While in isolated oligomers the azobenzene units undergo reversible photoisomerization independently, in the nanofibers they are coupled via intermolecular interactions and switch cooperatively as evidenced by unusual thermal and kinetic behavior. We find that the photoisomerization rate from the Z-isomer to the E-isomer depends on the fraction of Z-azobenzene in the nanofibers, and is increased by more than a factor of 4 in Z-rich fibers when compared to E-rich fibers. This demonstrates the great potential of coupling individual photochromic units for increasing their quantum efficiency in the solid state with potential relevance for actuation and sensing. PMID:27161608

  1. Dispersion of "guava-like" silica/polyacrylate nanocomposite particles in polyacrylate matrix

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    A series of "guava-like" silica/polyacrylate nanocomposite particles with close silica content and different grafting degrees were prepared via mini-emulsion polymerization using 3-(trimethoxysilyl)propyl methacrylate (TSPM) modified silica/acrylate dispersion.The silica/polyacrylate composite particles were melt-mixed with unfilled polyacrylate (PA) resin to prepare corresponding silica/polyacrylate molded composites and the dispersion mechanism of these silica particles from the "guava-like" composite particles into polyacrylate matrix was studied.It was calculated that about 110 silica particles were accumulated in the bulk of every silica/polyacrylate composite latex particle.Both the solubility tests of silica/polyacrylate composite latex particles in tetrahydrofuran (THF) and the section transmission electron microscope (TEM) micrographs of silica/polyacrylate molded composites indicated that the grafting degree of silica particles played a crucial role in the dispersion of silica/polyacrylate composite particles into the polyacrylate matrix.When the grafting degree of polyacrylate onto silica was in a moderate range (ca.20%-70%),almost all of silica particles in these "guava-like" composite particles were dispersed into the polyacrylate matrix in a primary-particle-level.However,at a lower grafting degree,massive silica aggregations were found in molded composites because of the lack of steric protection.At a greater grafting degree (i.e.,200%),a cross-linked network was formed in the silica/polyacrylate composite particles,which prevented the dispersion of composite particles in THF and polyacrylate matrix as primary particles.

  2. Rewritable azobenzene polyester for polarization holographic data storage

    DEFF Research Database (Denmark)

    Kerekes, A; Sajti, Sz.; Loerincz, Emoeke;

    2000-01-01

    Optical storage properties of thin azobenzene side-chain polyester films were examined by polarization holographic measurements. The new amorphous polyester film is the candidate material for the purpose of rewritable holographic memory system. Temporal formation of anisotropic and topographic...... erasing was tested. The ability of azobenzene polyester for rewriting was found satisfactory after many writing-erasing cycles....

  3. Optically induced surface relief phenomena in azobenzene polymers

    DEFF Research Database (Denmark)

    Holme, NCR; Nikolova, Ludmila; Hvilsted, Søren;

    1999-01-01

    Azobenzene polymers and oligomers show intriguing surface relief features when irradiated with polarized laser light. We show through atomic force microscopic investigation of side-chain azobenzene polymers after irradiation through an amplitude mask that large peaks or trenches result depending ...

  4. Binding of calcium and carbonate to polyacrylates.

    Science.gov (United States)

    Tribello, Gareth A; Liew, CheeChin; Parrinello, Michele

    2009-05-21

    Polyacrylate molecules can be used to slow the growth of calcium carbonate. However, little is known about the mechanism by which the molecules impede the growth rate. A recent computational study (Bulo et al. Macromolecules 2007, 40, 3437) used metadynamics to investigate the binding of calcium to polyacrylate chains and has thrown some light on the coiling and precipitation of these polymers. We extend these simulations to examine the binding of calcium and carbonate to polyacrylate chains. We show that calcium complexed with both carbonate and polyacrylate is a very stable species. The free energies of calcium-carbonate-polyacrylate complexes, with different polymer configurations, are calculated, and differences in the free energy of the binding of carbonate are shown to be due to differences in the amount of steric hindrance about the calcium, which prevents the approach of the carbonate ion. PMID:19400592

  5. Direct electrochemical oxidation of polyacrylates.

    Science.gov (United States)

    Bellagamba, Riccardo; Comninellis, Christos; Vatistas, Nicolaos

    2002-10-01

    A promising elimination treatment of non-biodegradable organic pollutants is the direct electro-oxidation. In this work has been proposed the electrochemical elimination of polyacrylates by using boron-doped diamond (BDD) as anodic material. The complete elimination of organic contaminants has been obtained and this is the first case of successful electrochemical treatment of polymeric and bio-refractory species. The tests of the electrochemical oxidation have been conducted at constant current conditions and a complete elimination of organic species has been reached. The decrease of the COD value with time follows the behaviour of an ideal anode as in the case of low molecular organic compounds. PMID:12489259

  6. Facile Synthesis of Au or Ag Nanoparticles-Embedded Hollow Carbon Microspheres from Metal-Organic Framework Hybrids and Their Efficient Catalytic Activities.

    Science.gov (United States)

    Choi, Sora; Lee, Hee Jung; Oh, Moonhyun

    2016-05-01

    Au or Ag nanoparticles-embedded hollow carbon spheres, which display outstanding catalytic activity and excellent recyclability, are prepared by a one-step pyrolysis of metal-organic framework (MOF) hybrids consisting of polystyrene cores and MOF shells loaded with noble metal ions (polystyrene@ZIF-8/M(n+) ; M(n+) = Au(3+) or Ag(+) ). PMID:27151828

  7. Silver nanoparticles embedded in amine-functionalized silicate sol-gel network assembly for sensing cysteine, adenosine and NADH

    Energy Technology Data Exchange (ETDEWEB)

    Maduraiveeran, Govindhan; Ramaraj, Ramasamy, E-mail: ramarajr@yahoo.com [Madurai Kamaraj University, Centre for Photoelectrochemistry, School of Chemistry (India)

    2011-09-15

    Silver nanoparticles embedded in amine-functionalized silicate sol-gel network were synthesized and used for sensing biomolecules such as cysteine, adenosine, and {beta}-nicotinamide adenine dinucleotide (NADH). The sensing of these biomolecules by the assembly of silver nanoparticles was triggered by the optical response of the surface plasmon resonance (SPR) of the silver nanoparticles. The optical sensor exhibited the lowest detection limit (LOD) of 5, 20, and 5 {mu}M for cysteine, adenosine, and NADH, respectively. The sensing of biomolecules in the micromolar range by using the amine-functionalized silicate sol-gel embedded silver nanoparticles was studied in the presence of interference molecules like uridine, glycine, guanine, and guanosine. Thus, the present approach might open up a new avenue for the development of silver nanoparticles-based optical sensor devices for biomolecules.

  8. Base effects on fabrication of silver nanoparticles embedded silica nanocomposite for surface-enhanced Raman scattering (SERS).

    Science.gov (United States)

    Kang, Homan; Kang, Taegyu; Kim, Seongyong; Kim, Jong-Ho; Jun, Bong-Hyun; Chae, Jinjoo; Park, Juyoung; Jeong, Dae-Hong; Lee, Yoon-Sik

    2011-01-01

    In this paper, we studied on the effect of organic bases in the case of ethylene glycol based fabrication of silver nanoparticles embedded silica nanocomposite (Ag SNC) without heating. Considering their chemical structures, butylamine (BA), ethanolamine (EA), triethanolamine (TEA), tributylamine (TBA), octylamine (OA) and Jeffamine 500 (JA) were used as an organic base. In addition, the effect of the concentrations of AgNO3 and organic bases on the formation of Ag SNC was also examined. In conformity with the characteristics of Ag SNC, SERS signal intensity of benzenethiol on Ag SNC was measured. As a result, the SERS signal intensity of Ag SNCs was strongly dependent on the reaction conditions. Furthermore, when reacted under the best reaction condition with concentrations of AgNO3 and OA, 3 mM and 5 mM, respectively, a large-scale production of Ag SNC was possible under the mild conditions. PMID:21446501

  9. An active nano-supported interface designed from gold nanoparticles embedded on ionic liquid for depositing DNA

    International Nuclear Information System (INIS)

    The use of an active nano-interface designed from gold nanoparticles embedded on ionic liquid for DNA damage resulted from formalehyde (HCHO) is reported in this article. The active nano-interface was fabricated by depositing gold nanoparticles on the ionic liquid 1-butyl-3-methylimidazolium tetrafluroborate ([bmim][BF4]). A glassy carbon electrode modified by this composite film was fabricated to immobilize DNA for probing into the damage resulted from HCHO. The modifying process was characterized by X-ray photoelectron spectroscopy, atomic force microscopy and electrochemistry involving electrochemical impedance spectroscopy. It was found that the modified film performs effectively in studying the DNA damage by electrocatalytic activity toward HCHO oxidation.

  10. Core-shell Au/Ag nanoparticles embedded in silicate sol-gel network for sensor application towards hydrogen peroxide

    Indian Academy of Sciences (India)

    Shanmugam Manivannan; Ramasamy Ramaraj

    2009-09-01

    The electrocatalytic activity of core-shell Au100-Ag ( = 15, 27, 46, and 60) bimetallic nanoparticles embedded in methyl functionalized silicate MTMOS network towards the reduction of hydrogen peroxide was investigated by using cyclic voltammetry and chronoamperometric techniques. Core-shell Au/Ag bimetallic nanoparticles were characterized by absorption spectra and HRTEM. The MTMOS silicate sol-gel embedded Au73Ag27 core-shell nanoparticles modified electrode showed better synergistic electrocatalytic effect towards the reduction of hydrogen peroxide when compared to monometal MTMOS-Aunps and MTMOS-Agnps modified electrodes. These modified electrodes were studied without immobilizing any enzyme in the MTMOS sol-gel matrix. The present study highlights the influence of molar composition of Ag nanoparticles in the Au/Ag bimetallic composition towards the electrocatalytic reduction and sensing of hydrogen peroxide in comparison to monometal Au and Ag nanoparticles.

  11. Plasmonic properties of Ag nanoparticles embedded in GeO2-SiO2 matrix by atom beam sputtering.

    Science.gov (United States)

    Mohapatra, Satyabrata

    2016-02-01

    Nanocomposite thin films containing Ag nanoparticles embedded in the GeO2-SiO2 matrix were synthesized by the atom beam co-sputtering technique. The structural, optical and plasmonic properties and the chemical composition of the nanocomposite thin films were studied by transmission electron microscopy (TEM) with energy dispersive X-ray spectroscopy (EDX), UV-visible absorption spectroscopy and X-ray photoelectron spectroscopy (XPS). UV-visible absorption studies on Ag-SiO2 nanocomposites revealed the presence of a strong localized surface plasmon resonance (LSPR) peak characteristic of Ag nanoparticles at 413 nm, which showed a blue shift of 26 nm (413 to 387 nm) along with a significant broadening and drastic decrease in intensity with the incorporation of 16 at% of Ge into the SiO2 matrix. TEM studies on Ag-GeO2-SiO2 nanocomposite thin films confirmed the presence of Ag nanoparticles with an average size of 3.8 nm in addition to their aggregates with an average size of 16.2 nm. Thermal annealing in air resulted in strong enhancement in the intensity of the LSPR peak, which showed a regular red shift of 51 nm (from 387 to 438 nm) with the increase in annealing temperature up to 500 °C. XPS studies showed that annealing in air resulted in oxidation of excess Ge atoms in the nanocomposite into GeO2. Our work demonstrates the possibility of controllably tuning the LSPR of Ag nanoparticles embedded in the GeO2-SiO2 matrix by single-step thermal annealing, which is interesting for optical applications. PMID:26766559

  12. Photochemical properties of multi-azobenzene compounds.

    Science.gov (United States)

    Bahrenburg, Julia; Sievers, Claudia M; Schönborn, Jan Boyke; Hartke, Bernd; Renth, Falk; Temps, Friedrich; Näther, Christian; Sönnichsen, Frank D

    2013-03-01

    A systematic study is reported of the photochemical properties of the multi-azobenzene compounds bis[4-(phenylazo)phenyl]amine (BPAPA) and tris[4-(phenylazo)phenyl]amine (TPAPA) compared to the parent molecule 4-aminoazobenzene (AAB). The bis- and tris-azobenzenes were synthesised by a variant of the Ullmann reaction and exist in their stable all-E forms at room temperature. Striking changes in the spectral positions and intensities of their first ππ* absorption bands compared to AAB reveal strong electronic coupling between the AB units. The nature of the excited states was explored by quantum chemical calculations at the approximate coupled-cluster (CC2) level. Upon UV/VIS irradiation, the molecules isomerise to the Z-isomer (AAB), ZE- and ZZ-isomers (BPAPA), and ZEE-, ZZE- and ZZZ-isomers (TPAPA), respectively. The photoswitching behaviours were investigated by UV/VIS and NMR spectroscopies. All individual isomers were detected by one-dimensional (1D) (1)H NMR spectroscopy (BPAPA) and two-dimensional (2D) HSQC NMR spectroscopy (TPAPA). A kinetic analysis provided the isomer-specific thermal lifetimes. The variance of the thermal lifetimes demonstrates a dependence of the Z-E isomerisation on the chromophore size and number of AB units. PMID:23224342

  13. Light scattering measurement of sodium polyacrylate products

    Science.gov (United States)

    Lama, Nisha; Norwood, David; Boone, Steven; Massie-Boyer, Valerie

    2015-03-01

    In the presentation, we will describe the use of a multi-detector HPLC incorporating the DAWN EOS multi-angle laser light scattering (MALLS) detector to measure the properties such as molecular weight, RMS radius, contour and persistence length and polydispersity of sodium polyacrylate products. The samples of sodium polyacrylate are used in various industries as thickening agents, coating dispersants, artificial snow, laundry detergent and disposable diapers. Data and results obtained from the experiment will be presented.

  14. The azobenzene optical storage puzzle - Demands on the polymer scaffold?

    DEFF Research Database (Denmark)

    Hvilsted, Søren; Ramanujam, P.S.

    2001-01-01

    The basic mechanism of optical information storage utilizing the azobenzene photoaddressable moiety will briefly be introduced. A synthetically flexible polyester matrix covalently integrating cyanoazobenzene in regularly spaced side chains is particularly well suited for holographic storage. Not...

  15. The Azobenzene Optical Storage Puzzle - Demands on the Polymer Scaffold?

    DEFF Research Database (Denmark)

    Hvilsted, Søren; Ramanujam, PS

    2001-01-01

    The basic mechanism of optical information storage utilizing the azobenzene photoaddressable moiety will briefly be introduced. A synthetically flexible polyester matrix covalently integrating cyanoazobenzene in regularly spaced side chains is particularly well suited for holographic storage. Not...

  16. Azobenzene-based Polymers for Solar Thermal Batteries

    Science.gov (United States)

    Venkataraman, Dhandapani

    Azobenzene exists as two isomers, a higher energy cis-isomer and a lower energy trans-isomer. The isomers interconvert under light or heat. Recently, there is a renewed interest in capturing the difference in the energies of the isomers and using azobenzene-based molecules as active layers for solar thermal batteries. My research group has been exploring azobenzene-based polymers as candidates for solar thermal batteries. In this talk, I will show that the azo-benzene moieties can be converted to the cis-form using light and converted back to the trans form using mechanical force. I will provide some of our recent results that indicate that high energy densities can be achieved in these polymers.

  17. Holographic Gratings in Azobenzene Side-Chain Polymethacrylates

    DEFF Research Database (Denmark)

    Andruzzi, Luisa; Altomare, Angelina; Ciardelli, Francesco; Solaro, Roberto; Hvilsted, Søren; Ramanujam, P.S.

    1999-01-01

    Optical storage properties of thin unoriented liquid crystalline and amorphous side-chain azobenzene polymethacrylate films are examined by polarization holographic measurements. The investigated materials are free radical copolymers derived from two photochromic monomers, 6-(4-oxy-4'-cyanoazoben......Optical storage properties of thin unoriented liquid crystalline and amorphous side-chain azobenzene polymethacrylate films are examined by polarization holographic measurements. The investigated materials are free radical copolymers derived from two photochromic monomers, 6-(4-oxy-4...

  18. Physical processes in azobenzene polymers on irradiation with polarized light

    DEFF Research Database (Denmark)

    Holme, N.C.R.; Nikolova, L.; Norris, T.B.;

    1999-01-01

    Azobenzenes can serve as model compounds for the study of trans-cis isomerization in more complex molecules. We have performed time-resolved spectroscopy in solutions containing free azobenzene chromophores and diols with a view to obtaining the energy levels and lifetimes of the excited states. A...... single beam transmission measurements through a mask, followed by atomic force microscope and profiler investigations. It is concluded that none of the prevalent theories can explain all the observed facts....

  19. Ultrasensitive photoreversible molecular sensors of azobenzene-functionalized plasmonic nanoantennas.

    Science.gov (United States)

    Joshi, Gayatri K; Blodgett, Karl N; Muhoberac, Barry B; Johnson, Merrell A; Smith, Kimberly A; Sardar, Rajesh

    2014-02-12

    This Letter describes an unprecedentedly large and photoreversible localized surface plasmon resonance (LSPR) wavelength shift caused by photoisomerization of azobenzenes attached to gold nanoprisms that act as nanoantennas. The blue light-induced cis to trans azobenzene conformational change occurs in the solid state and controls the optical properties of the nanoprisms shifting their LSPR peak up to 21 nm toward longer wavelengths. This shift is consistent with the increase in thickness of the local dielectric environment (0.6 nm) surrounding the nanoprism and perhaps a contribution from plasmonic energy transfer between the nanoprism and azobenzenes. The effects of the azobenzene conformational change and its photoreversibility were also probed through surface-enhanced Raman spectroscopy (SERS) showing that the electronic interaction between the nanoprisms and bound azobenzenes in their cis conformation significantly enhances the intensity of the Raman bands of the azobenzenes. The SERS data suggests that the isomerization is controlled by first-order kinetics with a rate constant of 1.0 × 10(-4) s(-1). Our demonstration of light-induced photoreversibility of this type of molecular machine is the first-step toward removing present limitations on detection of molecular motion in solid-state devices using LSPR spectroscopy with nanoprisms. Modulating the LSPR peak position and controlling energy transfer across the nanostructure-organic molecule interface are very important for the fabrication of plasmonic-based nanoscale devices. PMID:24393014

  20. Nonlinear optical properties of an azobenzene polymer

    International Nuclear Information System (INIS)

    The nonlinear optical properties of an azobenzene polymer azo12—MO were investigated by a Z-scan technique. The polymer was synthesized by assembling the liquid-crystalline polymer azo12 with methyl orange. The nonlinear refractive index (1.39 × 10−15 cm2/W) and the nonlinear absorption coefficient (0.11 cm/GW) of azo12—MO were determined with 532-nm picosecond laser pulses at the irradiance of 92.40 GW/cm2. When compared to the nonlinear properties of azo12 and methyl orange, azo12—MO possesses the advantages of its two constituents and shows larger nonlinear optical properties. (electromagnetism, optics, acoustics, heat transfer, classical mechanics, and fluid dynamics)

  1. Cobalt nanoparticles embedded in N-doped carbon as an efficient bifunctional electrocatalyst for oxygen reduction and evolution reactions

    Science.gov (United States)

    Su, Yunhe; Zhu, Yihua; Jiang, Hongliang; Shen, Jianhua; Yang, Xiaoling; Zou, Wenjian; Chen, Jianding; Li, Chunzhong

    2014-11-01

    Cobalt based catalysts are promising bifunctional electrocatalysts for both oxygen reduction and oxygen evolution reactions (ORR and OER) in unitized regenerative fuel cells (URFCs) operating with alkaline electrolytes. Here we report a hybrid composite of cobalt nanoparticles embedded in nitrogen-doped carbon (Co/N-C) via a solvothermal carbonization strategy. With the synergistic effect arising from the N-doped carbon and cobalt nanoparticles in the composite, the Co/N-C hybrid catalyst exhibits highly efficient bifunctional catalytic activity and excellent stability toward both ORR and OER. The ΔE (oxygen electrode activity parameter for judging the overall electrocatalytic activity of a bifunctional electrocatalyst) value for Co/N-C is 0.859 V, which is smaller than those of Pt/C and most of the non-precious metal catalysts in previous studies. Furthermore, the Co/N-C composite also shows better bifunctional catalytic activity than its oxidative counterparts, which could be attributed to the high specific surface area and the efficient charge transfer ability of the composite, as well as the good synergistic effect between N-doped carbon and the Co nanoparticles in the Co/N-C composite.Cobalt based catalysts are promising bifunctional electrocatalysts for both oxygen reduction and oxygen evolution reactions (ORR and OER) in unitized regenerative fuel cells (URFCs) operating with alkaline electrolytes. Here we report a hybrid composite of cobalt nanoparticles embedded in nitrogen-doped carbon (Co/N-C) via a solvothermal carbonization strategy. With the synergistic effect arising from the N-doped carbon and cobalt nanoparticles in the composite, the Co/N-C hybrid catalyst exhibits highly efficient bifunctional catalytic activity and excellent stability toward both ORR and OER. The ΔE (oxygen electrode activity parameter for judging the overall electrocatalytic activity of a bifunctional electrocatalyst) value for Co/N-C is 0.859 V, which is smaller than those

  2. Mechano-synthesis, structural and magnetic characterization, and heat release of α-Fe nanoparticles embedded in a wüstite matrix

    Science.gov (United States)

    Batista, S. O. S.; Morales, M. A.; Santos, W. C. dos; Iglesias, C. A.; Baggio-Saitovitch, E.; Carriço, A. S.; Bohn, F.; de Medeiros, S. N.

    2015-10-01

    We report a study of the structural and magnetic properties, as well as of the heat release, of an iron/wüstite composite, prepared from iron powder and water by high energy mechanical milling. We identify that the produced sample consists of α-Fe nanoparticles embedded in a wüstite matrix and has high stability in time. Moreover, we observe that it presents noticeable features, as exchange bias effect at low temperatures and, when an alternating magnetic field is applied, its temperature reaches ∼46 °C in ∼600 s. Thus, the results and the possibility of tuning the magnetic properties of α-Fe nanoparticles embedded in a wüstite matrix, through interface interactions, place this system as a very attractive candidate for biomedical applications such as magnetic hyperthermia agent for cancer therapy.

  3. Cobalt nanoparticle-embedded carbon nanotube/porous carbon hybrid derived from MOF-encapsulated Co3O4 for oxygen electrocatalysis.

    Science.gov (United States)

    Dou, Shuo; Li, Xingyue; Tao, Li; Huo, Jia; Wang, Shuangyin

    2016-08-11

    We successfully obtained a novel bi-functional electrocatalyst towards the ORR and OER: Co nanoparticle-embedded N-doped carbon nanotube (CNT)/porous carbon (PC) by pyrolyzing metal organic framework (MOF) encapsulated Co3O4. The as-obtained hybrid exhibited highly efficient electrocatalytic activity for the ORR and OER. Furthermore, the assembled Zn-air batteries also revealed promising performance and long-term stability. PMID:27411845

  4. 21 CFR 177.1211 - Cross-linked polyacrylate copolymers.

    Science.gov (United States)

    2010-04-01

    ... polyacrylate copolymers consist of: (1) The grafted copolymer of cross-linked sodium polyacrylate identified as... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Cross-linked polyacrylate copolymers. 177.1211... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1211 Cross-linked...

  5. Synthesis and characterization of PVP-capped CdSe nanoparticles embedded in PVA matrix for photovoltaic application

    International Nuclear Information System (INIS)

    Polyvinyl pyrrolidone (PVP) capped cadmium selenide (CdSe) nanoparticles embedded in polyvinyl alcohol (PVA) matrix are reported. PVP-CdSe nanoparticles are prepared by a non-aqueous method wherein cadmium chloride is used as the cadmium source and sodium selenate as the selenium source. The nanocomposites are characterized by x-ray diffraction (XRD) and transmission electron microscopy (TEM) studies. XRD and TEM studies show the formation of cubic CdSe particles with an average size of 2.3 ± 0.2 nm. The synthesized nanoparticles are dispersed in the PVA matrix and cast as self-standing flexible (PVP-CdSe)-PVA films. These films are characterized by optical absorption spectroscopy, by which optical band energy gaps as well as the average particle size of CdSe nanoparticles were calculated. The I-V characteristic curve of the (PVP-CdSe)-PVA film shows a photovoltaic cell-like behaviour. The electromotive force generated from the (PVP-CdSe)-PVA film as a function of light intensity was also studied.

  6. Enhancement in field emission current density of Ni nanoparticles embedded in thin silica matrix by swift heavy ion irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Sarker, Debalaya; Patra, Rajkumar; Srivastava, P.; Ghosh, S., E-mail: santanu1@physics.iitd.ac.in [Nanostech Laboratory, Department of Physics, Indian Institute of Technology Delhi, New Delhi 110016 (India); Kumar, H. [Nanostech Laboratory, Department of Physics, Indian Institute of Technology Delhi, New Delhi 110016 (India); Instituto de Física, Universidade de São Paulo, USP, 05508-090 São Paulo, SP (Brazil); Kabiraj, D.; Avasthi, D. K. [Inter University Accelerator Centre, New Delhi 110067 (India); Vayalil, Sarathlal K.; Roth, S. V. [DESY, Petra III, Hamburg (Germany)

    2014-05-07

    The field emission (FE) properties of nickel nanoparticles embedded in thin silica matrix irradiated with 100 MeV Au{sup +7} ions at various fluences are studied here. A large increase in FE current density is observed in the irradiated films as compared to their as deposited counterpart. The dependence of FE properties on irradiation fluence is correlated with surface roughness, density of states of valence band and size distribution of nanoparticles as examined with atomic force microscope, X-ray photoelectron spectroscopy, and grazing incidence small angle x-ray scattering. A current density as high as 0.48 mA/cm{sup 2} at an applied field 15 V/μm has been found for the first time for planar field emitters in the film irradiated with fluence of 5.0 × 10{sup 13} ions/cm{sup 2}. This significant enhancement in the current density is attributed to an optimized size distribution along with highest surface roughness of the same. This new member of field emission family meets most of the requirements of cold cathodes for vacuum micro/nanoelectronic devices.

  7. PdCo alloy nanoparticle-embedded carbon nanofiber for ultrasensitive nonenzymatic detection of hydrogen peroxide and nitrite.

    Science.gov (United States)

    Liu, Dong; Guo, Qiaohui; Zhang, Xueping; Hou, Haoqing; You, Tianyan

    2015-07-15

    PdCo alloy nanoparticle-embedded carbon nanofiber (PdCo/CNF) prepared by electrospinning and thermal treatment was employed as a high-performance platform for the determination of hydrogen peroxide and nitrite. The as-obtained PdCo/CNF were characterized by transmission electron microscopy, energy-dispersive X-ray spectroscopy and X-ray diffraction. Electrochemical impedance spectroscopy, cyclic voltammetry and differential pulse voltammetry were employed to investigate the electrochemical behaviors of the resultant biosensor. The proposed PdCo/CNF-based biosensor showed excellent analytical performances toward hydrogen peroxide (detection limit: 0.1 μM; linear range: 0.2 μM-23.5 mM) and nitrite (detection limit: 0.2 μM; linear range: 0.4-30 μM and 30-400 μM). The superior analytical properties could be attributed to the synergic effect and firmly embedment of well-dispersed PdCo alloy nanoparticles. These attractive electrochemical properties make this robust electrode material promising for the development of effective electrochemical sensors. PMID:25818356

  8. Two-Solvent Method Synthesis of NiO/ZnO Nanoparticles Embedded in Mesoporous SBA-15: Photocatalytic Properties Study.

    Science.gov (United States)

    Dai, Peng; Yan, Tao-Tao; Yu, Xin-Xin; Bai, Zhi-Man; Wu, Ming-Zai

    2016-12-01

    Different loadings of NiO/ZnO nanoparticles embedded in mesoporous silica (SBA-15) were prepared via a two-solvent method with the ordered hexagonal mesoporous structure of SBA-15 kept. X-ray diffraction, transmission electron microscope, X-ray photoelectron spectroscopy, diffusive reflective UV-vis spectroscopy, and N2 adsorption porosimetry were employed to characterize the nanocomposites. The results indicate that the ordered hexagonal mesoporous structure of SBA-15 is kept and the absorption band edges of the nanocomposites shift into the ultraviolet light regime. The photocatalytic activity of our samples for degradation of methylene orange was investigated under UV light irradiation, and the results show that the nanocomposites have higher photodegradation ability toward methylene orange than commercial pure P-25. The photocatalytic activity of the nanocomposites was found to be dependent on both the adsorption ability of the SBA-15 and the photocatalytic activity of NiO-ZnO nanoparticles encapsulated in SBA-15. In addition, there is an optimal loading of NiO-ZnO nanoparticles. Too high or low loading will lower the photodegradation ability of the nanocomposites. PMID:27119154

  9. Mechano-synthesis, structural and magnetic characterization, and heat release of α-Fe nanoparticles embedded in a wüstite matrix

    International Nuclear Information System (INIS)

    We report a study of the structural and magnetic properties, as well as of the heat release, of an iron/wüstite composite, prepared from iron powder and water by high energy mechanical milling. We identify that the produced sample consists of α-Fe nanoparticles embedded in a wüstite matrix and has high stability in time. Moreover, we observe that it presents noticeable features, as exchange bias effect at low temperatures and, when an alternating magnetic field is applied, its temperature reaches ∼46 °C in ∼600 s. Thus, the results and the possibility of tuning the magnetic properties of α-Fe nanoparticles embedded in a wüstite matrix, through interface interactions, place this system as a very attractive candidate for biomedical applications such as magnetic hyperthermia agent for cancer therapy. - Highlights: • We investigate the structural and magnetic properties, as well as the heat release, of an iron/wüstite composite. • The samples are produced using high energy mechanical milling. • Fe nanoparticles embedded in a wüstite matrix have high stability in time. • When an alternating magnetic field is applied, the sample temperature increases up to ∼46°C. • The composite is an interesting candidate for biomedical applications, such as magnetic hyperthermia agent for cancer therapy

  10. Mechano-synthesis, structural and magnetic characterization, and heat release of α-Fe nanoparticles embedded in a wüstite matrix

    Energy Technology Data Exchange (ETDEWEB)

    Batista, S.O.S.; Morales, M.A.; Santos, W.C. dos; Iglesias, C.A. [Departamento de Física Teórica e Experimental, Universidade Federal do Rio Grande do Norte, 59078-900 Natal, RN (Brazil); Baggio-Saitovitch, E. [Centro Brasileiro de Pesquisas Físicas, Rua Dr. Xavier Sigaud 150, Urca, 22290-180 Rio de Janeiro, RJ (Brazil); Carriço, A.S. [Departamento de Física Teórica e Experimental, Universidade Federal do Rio Grande do Norte, 59078-900 Natal, RN (Brazil); Bohn, F., E-mail: felipebohn@gmail.com [Departamento de Física Teórica e Experimental, Universidade Federal do Rio Grande do Norte, 59078-900 Natal, RN (Brazil); Medeiros, S.N. de [Departamento de Física Teórica e Experimental, Universidade Federal do Rio Grande do Norte, 59078-900 Natal, RN (Brazil)

    2015-10-01

    We report a study of the structural and magnetic properties, as well as of the heat release, of an iron/wüstite composite, prepared from iron powder and water by high energy mechanical milling. We identify that the produced sample consists of α-Fe nanoparticles embedded in a wüstite matrix and has high stability in time. Moreover, we observe that it presents noticeable features, as exchange bias effect at low temperatures and, when an alternating magnetic field is applied, its temperature reaches ∼46 °C in ∼600 s. Thus, the results and the possibility of tuning the magnetic properties of α-Fe nanoparticles embedded in a wüstite matrix, through interface interactions, place this system as a very attractive candidate for biomedical applications such as magnetic hyperthermia agent for cancer therapy. - Highlights: • We investigate the structural and magnetic properties, as well as the heat release, of an iron/wüstite composite. • The samples are produced using high energy mechanical milling. • Fe nanoparticles embedded in a wüstite matrix have high stability in time. • When an alternating magnetic field is applied, the sample temperature increases up to ∼46°C. • The composite is an interesting candidate for biomedical applications, such as magnetic hyperthermia agent for cancer therapy.

  11. Actuation response of polyacrylate dielectric elastomers

    DEFF Research Database (Denmark)

    Kofod, G.; Kornbluh, R.; Pelrine, R.;

    2001-01-01

    Polyacrylate dielectric elastomers have yielded extremely large strain and elastic energy density suggesting that they are useful for many actuator applications. A thorough understanding of the physics underlying the mechanism of the observed response to an electric field can help develop improved...

  12. Photo-induced fluorescence emission enhancement of azobenzene thin films

    OpenAIRE

    Haruta, Osamu; Matsuo, Yasutaka; Ijiro, Kuniharu

    2008-01-01

    UV irradiation-induced fluorescence enhancement of thin films composed of azobenzene amphiphiles, C12AzoC10N+ (AzoN+), was investigated. UV irradiation to Langmuir-Blodgett (LB) monolayers of AzoN+ indicated that the fluorescence emission from an irradiated area was enhanced and the emission was independent of the aggregation structures of an azobenzene moiety. Moreover, UV irradiation to cast films of AzoN+ revealed that the enhancement was increased by increasing the irradiation time. The f...

  13. Two-solvent method synthesis of SnO{sub 2} nanoparticles embedded in SBA-15: Gas-sensing and photocatalytic properties study

    Energy Technology Data Exchange (ETDEWEB)

    Dai, Peng; Zhang, Lili; Li, Guang; Sun, Zhaoqi [Key Laboratory of Information Materials and Device, School of Physics and Materials Science, Anhui University, Hefei 230039 (China); Liu, Xiansong [Engineering Technology Research Center of Magnetic Materials, Hefei 230039 (China); Wu, Mingzai, E-mail: mingzaiwu@gmail.com [Key Laboratory of Information Materials and Device, School of Physics and Materials Science, Anhui University, Hefei 230039 (China); Engineering Technology Research Center of Magnetic Materials, Hefei 230039 (China)

    2014-02-01

    Graphical abstract: Different loadings of SnO{sub 2} nanoparticles embedded in mesoporous silica (sample S1, S2 and S3) show higher response to H{sub 2} at lower operating temperature than pure SnO{sub 2} nanoparticles. - Highlights: • Two-solvent method is firstly used to synthesize SnO{sub 2} nanoparticles embedded in mesoporous silica (SBA-15). • The SnO{sub 2}/SBA-15 nanocomposites show higher response to H{sub 2} at lower operating temperature than pure SnO{sub 2} nanoparticles. • The SnO{sub 2}/SBA-15 nanocomposites have higher photodegradation ability toward methylene blue than pure SnO{sub 2} nanoparticles. - Abstract: Different loadings of SnO{sub 2} nanoparticles embedded in mesoporous silica (SBA-15) were prepared via a two-solvent method with the ordered hexagonal mesoporous structure of SBA-15 kept. X-ray diffraction, transmission electron microscope, X-ray photoelectron spectroscopy and N{sub 2} adsorption porosimetry were employed to characterize the nanocomposites. Compared with pure SnO{sub 2} nanoparticles, the SnO{sub 2}/SBA-15 nanocomposites show higher response to H{sub 2} at lower operating temperature. The photocatalytic activity of as-prepared SnO{sub 2}/SBA-15 for degradation of methylene blue was investigated under UV light irradiation and the results show that the SnO{sub 2}/SBA-15 nanocomposites have higher photodegradation ability toward methylene blue than pure SnO{sub 2} nanoparticles.

  14. Colorimetric Sugar Sensing Using Boronic Acid-Substituted Azobenzenes

    Directory of Open Access Journals (Sweden)

    Yuya Egawa

    2014-02-01

    Full Text Available In association with increasing diabetes prevalence, it is desirable to develop new glucose sensing systems with low cost, ease of use, high stability and good portability. Boronic acid is one of the potential candidates for a future alternative to enzyme-based glucose sensors. Boronic acid derivatives have been widely used for the sugar recognition motif, because boronic acids bind adjacent diols to form cyclic boronate esters. In order to develop colorimetric sugar sensors, boronic acid-conjugated azobenzenes have been synthesized. There are several types of boronic acid azobenzenes, and their characteristics tend to rely on the substitute position of the boronic acid moiety. For example, o-substitution of boronic acid to the azo group gives the advantage of a significant color change upon sugar addition. Nitrogen-15 Nuclear Magnetic Resonance (NMR studies clearly show a signaling mechanism based on the formation and cleavage of the B–N dative bond between boronic acid and azo moieties in the dye. Some boronic acid-substituted azobenzenes were attached to a polymer or utilized for supramolecular chemistry to produce glucose-selective binding, in which two boronic acid moieties cooperatively bind one glucose molecule. In addition, boronic acid-substituted azobenzenes have been applied not only for glucose monitoring, but also for the sensing of glycated hemoglobin and dopamine.

  15. The Volume Holographic Optical Storage Potential in Azobenzene Containing Polymers

    DEFF Research Database (Denmark)

    Hvilsted, Søren; Sanchez, Carlos; Alcalá, Rafael

    2009-01-01

    suitable for holographic storage applications. However, they still present several problems, mainly those related with light sensitivity, response time and stability of the stored information. In this article we review the work performed on volume holographic storage using azobenzene containing polymers as...

  16. Pattern Formation and Quasicrystal Structure in Azobenzene Polymer Film

    Institute of Scientific and Technical Information of China (English)

    XU Ze-Da; CAI Zhi-Gang; ZHANG Ling-Zhi; LIU Yan-Fa; YANG Jie; SHE Wei-Long; ZHOU Jian-Ying

    2000-01-01

    Pattern formation in azobenzene polymer film by degenerate four-wave mixing is reported. Island arrays with specific patterns are analyzed with scanning electron microscopy and polarizing optical microscopy. It is demonstrated that the control of photo-induced nanostructure sized micropattern in the nonlinear organic film is possible by using properly polarized writing beams with the total incident power exceeding a certain threshold.

  17. Photoinduced Circular Anisotropy in Side-Chain Azobenzene Polyesters

    DEFF Research Database (Denmark)

    Nikolova, L.; Todorov, T.; Ivanov, M.;

    1997-01-01

    We report for the first time the inducing of large circular anisotropy in previously unoriented films of side-chain azobenzene polyesters on illumination with circularly polarized light at a wavelength of 488 nm. The circular dichroism and optical activity are measured simultaneously in real time...

  18. Polarisation-sensitive optical elements in azobenzene polyesters and peptides

    DEFF Research Database (Denmark)

    Ramanujam, P.S.; Dam-Hansen, Carsten; Berg, Rolf Henrik;

    2006-01-01

    In this article, we describe fabrication of polarisation holographic optical elements in azobenzene polyesters. Both liquid crystalline and amorphous side-chain polyesters have been utilised. Diffractive optical elements such as lenses and gratings that are sensitive to the polarisation of the in...

  19. Photo-orientation in azobenzene containing polybutadiene based polymer

    Czech Academy of Sciences Publication Activity Database

    Rais, David; Nešpůrek, Stanislav; Zakrevskyy, Y.; Stumpe, J.; Sedláková, Zdeňka; Studenovský, Martin

    2005-01-01

    Roč. 7, č. 3 (2005), s. 1371-1375. ISSN 1454-4164 R&D Projects: GA AV ČR IAA4112401 Institutional research plan: CEZ:AV0Z40500505 Keywords : azobenzene * polybutadien * photo-orientation Subject RIV: CD - Macromolecular Chemistry Impact factor: 1.138, year: 2005

  20. INAA of polyacrylic hydrogels of pharmaceutical grade

    International Nuclear Information System (INIS)

    Polyacrylic acid (PA) and its salts are promising biomaterials used in the pharmaceutical industry. They could be used as pharmaceutical additives, as a burn dressing and also in the slow released implants or trans-derma patch formulations. Polyacrylic acid of pharmaceutical grade can be obtained by gamma irradiation polymerization. The influence of the raw materials and of the technological procedure on the final product purity has been investigated by Instrumental Neutron Activation Analysis (INAA) method. The following materials have been analyzed by INAA: 1) acrylic acid of technical grade; 2) acrylic acid purified by double crystallisation; 3) NaOH of analytical grade; 4) CaCl-2·6H2O of pharmaceutical grade; 5) CaCl2·2H2O of analytical grade; 6) granulated PANa; 7) ungranulated PANa; 8) ungranulated PANaCa; 9) PANaCa granulated by milling in IFIN-HH using the mill nr. 1; 10) PANaCa granulated by milling in Institute of Chemical and Pharmaceutical Research (ICPR); 11) PANaCa granulated by milling in IFIN-HH using the mill nr. 2. The first five samples, marked from 1 to 5, are raw materials and the other six samples, marked from 6 to 11, are the final polyacrylic structures processed by various technological procedures. The samples together with the appropriate reference materials have been irradiated at WWR-S reactor in a neutron flux of 2.5·1012 cm-2s-1 and the induced radioactivity was registered by a HPGe detector (EG/G ORTEC) of 30% efficiency and 2.1 keV resolution. The concentrations of As, Br, Ce, Co, Cr, Fe, La, Sb, Sc, Zn have been determined. For the final polyacrylic structures, except for granulated PANa (sample 6), only the elements Co, Cr, Fe, Sc, Zn were found at the following concentration levels: tens of ppm (Co), ppm (Zn), hundreds of ppb (Cr), tens of ppb (Co), ppb (Co, Sc), 10-1 ppb (Sc). In the granulated PANa, in comparison with the other analyzed final products, similar concentration values were found for Fe, Sc and Zn, higher values

  1. Quantum theory and experimental studies of absorption spectra and photoisomerization of azobenzene polymers

    DEFF Research Database (Denmark)

    Pedersen, Thomas Garm; Ramanujam, P.S.; Johansen, P.M.;

    1998-01-01

    The microscopic properties of azobenzene chromophores are important for a correct description of optical storage systems based on photoinduced anisotropy in azobenzene polymers. A quantum model of these properties is presented and verified by comparison to experimental absorption spectra for trans...... and cis isomers of cyano methoxy azobenzene. In addition, the trans --> cis quantum efficiency is measured, and hence the combined experimental and theoretical work allows one to determine the essential molecular properties, including magnitude and anisotropy of the absorption cross section and...

  2. Geometry Control of Photo-induced Microstructures in an Azobenzene Polymer Film

    Institute of Scientific and Technical Information of China (English)

    Xu Ze-Da; LI Zhen; LIANG Li-Zhen; PENG Zhuo-Lun; CAI Zhi-Gang; ZHOU Jian-Ying; NINULESCU Valerica; ZHANG Ling-Zhi

    2001-01-01

    The mechanisms of photo-induced microstructures in an azobenzene polymer film are presented. They are based on the spatial periodic modulation of optical intensity and the photoisomerization of azobenzene molecules with the movement of main chains. Experiment and theory jointly point out the possibility of photo-inducing desired spatial microstructures in an azobenzene organic polymer via adequate optical lattices and adequately polarized ‘writing' beams.

  3. Surface relief measurements in side-chain azobenzene polyesters with different substituents

    DEFF Research Database (Denmark)

    Helgert, M.; Wenke, L.; Hvilsted, Søren;

    2001-01-01

    Light-induced surface modification of a series of liquid-crystalline side-chain azobenzene polyesters which have the same main- and side-chain structure but eleven different substituents on the azobenzene is investigated. Using a transmission mask as well as single focused beams we show that the...... azobenzene polyester was included in the study for comparison. The results point to a mechanism of the surface relief phenomenon, in which the architecture of the polyesters plays a crucial role....

  4. Influence of hydrogen bonding on the generation and stabilization of liquid crystalline polyesters, poly(esteramide)s and polyacrylates

    Indian Academy of Sciences (India)

    C K S Pillai; K Y Sandhya; J D Sudha; M Saminathan

    2003-08-01

    Induction and stabilization of liquid crystallinity through hydrogen bonding (HB) are now well-established. Interesting observations made on the influence of HB on LC behaviour of amido diol-based poly(esteramide)s, poly(esteramide)s containing nitro groups and azobenzene mesogen-based polyacrylates will be discussed. The use of amido diol as an important precursor for the synthesis of novel PEAs containing inbuilt di-amide linkage enabled generation of extensive hydrogen bondings between the amide–amide and amide–ester groups which stabilized the mesophase structures of the PEAs. The contributions of hydrogen bonding to the generation and stabilization of mesophase structures were plainly evident from the observation of liquid crystallinity even in PEAs prepared from fully aliphatic amido diols. Replacement of terephthaloyl units by isophthaloyl moiety totally vanquished liquid crystalline phases while biphenylene and naphthalene units did only reduce the transition temperatures as expected. The occurrence of the smectic phases in some of the polymers indicated possibly self-assembly through the formation of hetero intermolecular hydrogen bonded networks. A smectic polymorphism and in addition, a smectic-to-nematic transition, were observed in the monomers and polymers based on 1,4-phenylene[bis-(3-nitroanthranilidic acid)] containing nitro groups. A smectic polymorphism was also observed as a combined effect of hydrogen bonded carboxyl groups and laterally substituted alkyl side chains in the case of azobenzene mesogen containing side chain polyacrylates. It was further shown that the presence of the mesophase enhances the non-linear optical (NLO) response of these polymers.

  5. Industrial solution contaminated by polyacrylates: their elimination by electrochemical combustion.

    Science.gov (United States)

    Masci, M; Chiti, L; De Lorenzo, A; Mantione, D; De Battisti, A; Vatistas, N

    2001-01-01

    The electrochemical combustion of polyacrylates was studied through both direct and indirect oxidation. The obtained results indicate the non elimination of the polyacrylates with the direct oxidation, while the indirect oxidation with NaCl completely eliminates these organic compounds. In the last case the effects of different initial concentrations of NaCl, anode materials and current densities was studied. PMID:11381543

  6. Holographic Gratings in Azobenzene Side-Chain Polymethacrylates

    DEFF Research Database (Denmark)

    Andruzzi, Luisa; Altomare, Angelina; Ciardelli, Francesco;

    1999-01-01

    Optical storage properties of thin unoriented liquid crystalline and amorphous side-chain azobenzene polymethacrylate films are examined by polarization holographic measurements. The investigated materials are free radical copolymers derived from two photochromic monomers, 6-(4-oxy-4'-cyanoazoben......Optical storage properties of thin unoriented liquid crystalline and amorphous side-chain azobenzene polymethacrylate films are examined by polarization holographic measurements. The investigated materials are free radical copolymers derived from two photochromic monomers, 6-(4-oxy-4...... polarizing optical microscopy. Atomic force microscopy investigations have been carried out on the polarization holographic gratings recorded in the polymethacrylate films. A surface relief grating has been found to appear in all films after irradiation. The copolymers with 50-75% dye content exhibit the...

  7. Synthesis and characterization of termini azobenzene-dendrimer

    Directory of Open Access Journals (Sweden)

    Omid Louie

    2013-10-01

    Full Text Available Some of the organic molecules can be isomerized upon photoirradiation and when they are accompanied by a change in the visible absorption spectrum, it can be called photochromism. Azobenzenes which are important parts of molecular machines and nanotechnology can be called photoisomerizationazobenzene (azo chromophores, and have been incorporated into a wide variety of materials and molecular architectures, including polymers, dendrimers, and molecular glasses. We synthesized and characterized the AB2 type polyamidoamine (PAMAM dendrimers by single active site. PAMAM diazobenzenedendrimer was synthesized and characterized by FTIR and NMR (1H, 13C and CHN-O Elementary analysis. A simple method can be used for the synthesis of azobenzene derivative PAMAM dendrimer and other similar compounds.

  8. Preparation and Nonlinear Optical Property of Azobenzene Substituted Polyacetylene

    Institute of Scientific and Technical Information of China (English)

    Shou Chun YIN; Gang LI; Hong Yao XU; Ya Chen GAO; Yin Lin SONG

    2005-01-01

    Two new functional polyacetylenes bearing different azobenzene group, -{ HC=C[azo-N(CH3)CH2CH2OH] } n-, [poly(EHAB); azo = 4,4'-azobenzene] and - { HC=C[azo-N(CH3)CH2CH2OCOC3H7]}n-, [poly(EEAB)]} were prepared by [Rh(nbd)Cl]2-Et3N catalysts. Poly(EHAB) has poor solubility while poly(EEAB) can be dissolved in common solvent. The polymers were characterized by FTIR, 1H NMR, UV and GPC. The nonlinear optical property of the soluble poly(EEAB) was investigated with 8 ns width pulse at 532 nm by Z-scan technique. The results show that poly(EEAB) is endowed with the larger third-order nonlinear optical property.

  9. Polymer scaffolds bearing azobenzene - Potential for optical information storage

    DEFF Research Database (Denmark)

    Hvilsted, Søren; Ramanujam, P.S.

    2001-01-01

    The fundamental optical storage mechanism of the laser light addressable azobenzene moiety is briefly introduced. A modular and flexible synthesis design furnishes polyester matrices covalently integrating cyanoazobenzene in regularly spaced side chains. Thin films of these materials are particul......The fundamental optical storage mechanism of the laser light addressable azobenzene moiety is briefly introduced. A modular and flexible synthesis design furnishes polyester matrices covalently integrating cyanoazobenzene in regularly spaced side chains. Thin films of these materials are...... particularly well suited for holographic storage. Notable figures of merits of liquid crystalline polyesters are response time to blue-green laser light of the order of nanoseconds, storage capacity expressed as 5000 lines/mm, and high, permanent (almost nine years) diffraction efficiency of the order of 50...

  10. Glycosylated polyacrylate nanoparticles by emulsion polymerization

    OpenAIRE

    Abeylath, Sampath C.; Turos, Edward

    2007-01-01

    A selection of glycosylated polyacrylate nanoparticles has been prepared by radical-initiated emulsion polymerization in aqueous media. Using ethyl acrylate as a co-monomer, carbohydrate acrylates were incorporated into the poly(ethyl acrylate) framework to give stable emulsions of glyconanoparticles with an average particle size of around 40 nm. Using this technique a variety of glyconanoparticles were prepared from 3-O-acryloyl-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose, 1-O-acryloyl-2,3...

  11. Light-controlled anisotropy in dielectrics containing azobenzene

    Czech Academy of Sciences Publication Activity Database

    Rais, David; Nešpůrek, Stanislav; Sedláková, Zdeňka; Zakrevskyy, Y.; Stumpe, J.

    Vol. Nr 982. Lodz : Department of Molecular Physics, Technical University of Lodz, 2006 - (Socha, A.), s. 270-271 ISSN 0458-1555. [Conference International Dielectric Society /4./ and International Conference Dielectric and Related Phenomena /9./. Poznan (PL), 03.09.2006-07.09.2006] R&D Projects: GA AV ČR IAA4112401 Institutional research plan: CEZ:AV0Z40500505 Keywords : azobenzene * light anisotropy * photochromism Subject RIV: CD - Macromolecular Chemistry

  12. Propagation of polarized light through azobenzene polyester films

    DEFF Research Database (Denmark)

    Nedelchev, L; Matharu, A; Nikolova, Ludmila;

    2002-01-01

    When elliptically polarized light of appropriate wavelength Corresponding to trans-cis-trans isomerisation process is incident on thin films of azobenzene polyesters, a helical structure is induced. We investigate the propagation of the exciting light beam (self-induced) as well as a probe light...... beam outside the absorption band through the polyester films. Investigations are carried out in one amorphous and one liquid crystalline polyester. We show that amorphous polyester after irradiation behaves like classical helical material....

  13. Photoinduced orientation in photochromic polybutadiene containing azobenzene side groups

    Czech Academy of Sciences Publication Activity Database

    Rais, David; Nešpůrek, Stanislav; Zakrevskyy, Y.; Stumpe, J.; Sedláková, Zdeňka; Combellas, C.; Kajzar, F.

    Barcelona : COST Chemistry and Institut de Ciencia de Materials de Barcelona, 2005. s. 67. [Final Evaluation Conference of the Chemistry COST Action D14 ‘Functional Molecular Materials’. 9.6.2005-12.6.2005, San Feliu de Guixols] R&D Projects: GA MŠk 1P04OCD14.30; GA AV ČR IAA4112401 Keywords : azobenzene * photochromic Subject RIV: CD - Macromolecular Chemistry

  14. Dicyclopalladated complexes of asymmetrically substituted azobenzenes: synthesis, kinetics and mechanisms.

    Science.gov (United States)

    Juribašić, Marina; Budimir, Ana; Kazazić, Snježana; Curić, Manda

    2013-11-01

    Two series of new dicyclopalladated complexes {(DMF)PdCl(μ-R(1)C6H3N═NC6H3R(2))PdCl(DMF)} of 4,4'-functionalized azobenzenes with substituents of varying electron-donating or electron-withdrawing strength (R(1) = H, NMe2; R(2) = H, Cl, Br, I, OMe, PhNH, CO2H, SO3Na, or NO2) have been synthesized and fully characterized. (1)H NMR spectroscopy along with the ESI mass spectrometry unambiguously identified the new complexes in the solution, and their solid-state structures were determined by X-ray crystallography. The presence of easily exchangeable solvent ligands was confirmed by (1)H NMR spectroscopy, X-ray experiments, and ESI mass spectrometry. The complexes were additionally characterized by UV-vis and fluorescence spectroscopies. The effect of different 4,4'-substituents on the formation rate of mono- and dicyclopalladated azobenzenes was studied by UV-vis spectroscopy. The experimental results are complemented by the quantum-chemical (DFT) calculations in order to rationalize the kinetic results as well as substituent effects on the reaction rates. It was found that the mono- and dicyclopalladation reactions of azobenzenes proceed in two consecutive processes, adduct formation and palladation steps. The rate-determining step in both palladations is the breaking of the ortho C-H bond, which has been confirmed as an electrophilic substitution process by Hammett correlations and DFT calculations. PMID:24116960

  15. UV/EB crosslinked polyacrylate nanocomposites

    International Nuclear Information System (INIS)

    Nano-sized silica particles were used as fillers for acrylates. Because of their nanometer size and large active surface area radiation cross-linked polyacrylate nanocomposites exhibit markedly improved properties as compared to pure polymers: increased modulus and heat resistance, improved scratch and abrasion resistance as well as reduced gas permeability. This makes them very promising as coatings for technical applications. For favorable embedding of the silica particles within the acrylate matrix the surface of the fillers was chemically modified by reaction with organosilanes such as methacryloxypropyl trimethoxysilane or vinyl trimethoxysilane. As product of a acid catalysed condensation of the organosilanes a polysiloxane shell is formed which is linked to the silica surface via reaction with surface OH groups. The formation of covalent Si-O-Si-R bonds by condensation of silanes and/or by reaction with OH groups on silica was demonstrated by multinuclear MAS NMR, diffuse reflectance FTIR and XPS. From the tentative proposed substructures of the polysiloxane shell, mainly bidental and tridental surface complexes were identified by NMR. These findings are in accordance with fragmentation pattern of the polysiloxane shell as measured by MALDI-TOF. The REM image shows a typical surface topology of a polyacrylate nanocomposite. It can be seen that agglomerates are embedded within the organic matrix. However, coatings with a thickness up to 50 μm remain transparent

  16. Thin Film Encapsulation of Light-Emitting Diodes with Photopolymerized Polyacrylate and Silver Films

    Institute of Scientific and Technical Information of China (English)

    WANG Li-Duo; WU Zhao-Xin; LI Yang; QIU Yong

    2005-01-01

    @@ A thin film encapsulation of organic light-emitting diodes (OLEDs) is investigated with a multi-layer stack of polyacrylate-Ag-polyacrylate-Ag-polyacrylate-Ag-polyacrylate (PAPAPAP). It is shown that the fabrication of polyacrylate films by a wet process does not affect the electroluminescent (EL) characteristics of the devices and polyacrylate films together with the silver layers can perform to minimize oxygen and water diffusion into the organic light-emitting device. The structure of polyacrylate(20 μm)-Ag(200nm)-polyacrylate(20 μm)-Ag(200nm)-polyacrylate(20μm)-Ag(200nm)-polyacrylate(20μm) is demonstrated to enhance dramatically the lifetime of OLEDs.

  17. Plasmonic modification of electron-longitudinal-optical phonon coupling in Ag-nanoparticle embedded InGaN/GaN quantum wells

    Energy Technology Data Exchange (ETDEWEB)

    Llopis, Antonio; Neogi, Arup, E-mail: arup@unt.edu [Department of Physics, University of North Texas, Denton, Texas 76203 (United States); Pereira, Sérgio M. S. [Department of Physics, CICECO, Universidade de Aveiro, 3810-193 Aveiro (Portugal); Watson, Ian M. [Institute of Photonics, University of Strathclyde, Wolfson Centre, 106 Rottenrow East, Glasgow G4 0NW (United Kingdom)

    2014-09-01

    Surface plasmon enhanced GaN and InGaN quantum wells (QWs) show promise for use as room-temperature light emitters. The effectiveness of the plasmon enhancement, however, is limited by the strong electron/hole and longitudinal optical phonon coupling found in the III-V nitrides. The electron-phonon coupling within semiconductor QWs has been modified using silver nanoparticles embedded within the QWs. Direct evidence is provided for this change via confocal Raman spectroscopy of the samples. This evidence is augmented by Angle-dependent photoluminescence experiments which show the alteration of the electron-phonon coupling strength through measurement of the emitted phonon replicas. Together these demonstrate a direct modification of carrier-phonon interactions within the system, opening up the possibility of controlling the coupling strength to produce high-efficiency room-temperature light emitters.

  18. Preparation and optical characteristics of layered perovskite-type lead-bromide-incorporated azobenzene chromophores

    Energy Technology Data Exchange (ETDEWEB)

    Sasai, Ryo, E-mail: rsasai@riko.shimane-u.ac.jp [Department of Applied Chemistry, Graduate School of Engineering, Nagoya University, F3-3(250), Furo-cho, Chikusa-ku, Nagoya 464-8603 (Japan); Shinomura, Hisashi [Department of Applied Chemistry, Graduate School of Engineering, Nagoya University, F3-3(250), Furo-cho, Chikusa-ku, Nagoya 464-8603 (Japan)

    2013-02-15

    Lead bromide-based layered perovskite powders with azobenzene derivatives were prepared by a homogeneous precipitation method. From the diffuse reflectance (DR) and photoluminescence (PL) spectra of the hybrid powder materials, the present hybrids exhibited sharp absorption and PL peaks originating from excitons produced in the PbBr{sub 4}{sup 2-} layer. When the present hybrid powder was irradiated with UV light at 350 nm, the absorption band from the trans-azobenzene chromophore, observed around 350 nm, decreased, while the absorption band from the cis-azobenzene chromophore, observed around 450 nm, increased. These results indicate that azobenzene chromophores in the present hybrid materials exhibit reversible photoisomerization. Moreover, it was found that the PL intensity from the exciton also varied due to photoisomerization of the azobenzene chromophores in the present hybrid. Thus, for the first time we succeeded in preparing the azobenzene derivative lead-bromide-based layered perovskite with photochromism before and after UV light irradiation. - Graphical abstract: For the first time, we succeeded in preparing the azobenzene derivative lead-bromide-based layered perovskite with photochromism before and after UV light irradiation. Highlights: Black-Right-Pointing-Pointer PbBr-based layered perovskite with azobenezene derivatives could be synthesized by a homogeneous precipitation method. Black-Right-Pointing-Pointer Azobenzene derivatives incorporated the present hybrid that exhibited reversible photoisomerization under UV and/or visible light irradiation. Black-Right-Pointing-Pointer PL property of the present hybrid could also be varied by photoisomerization.

  19. Preparation and optical characteristics of layered perovskite-type lead-bromide-incorporated azobenzene chromophores

    International Nuclear Information System (INIS)

    Lead bromide-based layered perovskite powders with azobenzene derivatives were prepared by a homogeneous precipitation method. From the diffuse reflectance (DR) and photoluminescence (PL) spectra of the hybrid powder materials, the present hybrids exhibited sharp absorption and PL peaks originating from excitons produced in the PbBr42− layer. When the present hybrid powder was irradiated with UV light at 350 nm, the absorption band from the trans-azobenzene chromophore, observed around 350 nm, decreased, while the absorption band from the cis-azobenzene chromophore, observed around 450 nm, increased. These results indicate that azobenzene chromophores in the present hybrid materials exhibit reversible photoisomerization. Moreover, it was found that the PL intensity from the exciton also varied due to photoisomerization of the azobenzene chromophores in the present hybrid. Thus, for the first time we succeeded in preparing the azobenzene derivative lead-bromide-based layered perovskite with photochromism before and after UV light irradiation. - Graphical abstract: For the first time, we succeeded in preparing the azobenzene derivative lead-bromide-based layered perovskite with photochromism before and after UV light irradiation. Highlights: ► PbBr-based layered perovskite with azobenezene derivatives could be synthesized by a homogeneous precipitation method. ► Azobenzene derivatives incorporated the present hybrid that exhibited reversible photoisomerization under UV and/or visible light irradiation. ► PL property of the present hybrid could also be varied by photoisomerization.

  20. Kinetic analysis of the thermal isomerisation pathways in an asymmetric double azobenzene switch

    NARCIS (Netherlands)

    Robertus, Jort; Reker, Siebren F.; Pijper, Thomas C.; Deuzeman, Albert; Browne, Wesley R.; Feringa, Ben L.

    2012-01-01

    Here we report a photochemical and kinetic study of the thermal relaxation reaction of a double azobenzene system, in which two azobenzene photochromic units are connected via a phenyl ring. Upon UV irradiation, three thermally unstable isomers are formed. Kinetic studies using arrayed H-1-NMR spect

  1. DESIGN AND STUDY OF NEW AZOBENZENE LIQUID CRYSTAL/POLYMER MATERIALS

    Institute of Scientific and Technical Information of China (English)

    Yue Zhao

    2003-01-01

    Discussion is presented on the use of the photoisomerization of azobenzene chromophore in the design and preparation of novel functional materials. The two systems reviewed are azobenzene polymer-stabilized liquid crystals and azobenzene elastomers. In the first case, a polymer network containing azobenzene moieties is used to optically induce and stabilize a long-range liquid crystal orientation without the need of treating the surfaces of the substrates. This optical and rubbing-free approach was applied to nematic and ferroelectric liquid crystals. In the second case, an azobenzene side-chain liquid crystalline polymer is grafted onto a styrene-butadiene-styrene triblock copolymer to yield a photoactive thermoplastic elastomer. Coupled mechanical and optical effects make possible the formation of diffraction gratings that may be useful for mechanically tunable optical devices.

  2. Damping properties of silicone rubber/polyacrylate sequential interpenetrating networks

    Institute of Scientific and Technical Information of China (English)

    WANG Yan-bing; HUANG Zhi-xiong; ZHANG Lian-meng

    2006-01-01

    Silicone rubber/polyacrylate sequential interpenetrating polymer networks(IPNs) were prepared by silicone rubber sheet dipped into the solution composed of different acrylate monomers and benzoyl peroxides(BPOs) for different time at room temperature and then acrylate polymerized at 80 ℃ for 2 h. The molecular structure and damping properties of sequential IPNs were studied by means of FT-IR and dynamic mechanical analysis(DMA),respectively. The FT-IR spectrum shows that polyacrylate distributes unevenly along the thickness direction of IPNs,i.e. the concentration of polyacrylate decreases from the midst to the surface of the IPNs. The DMA shows that cold crystallization of silicone in the temperature range from -47 ℃ to -30 ℃ is reduced and loss factor of IPNs is improved after interpenetrating with polyacrylate. This suggestes that IPNs can be used as damping materials.

  3. Tuning the Photoinduced Motion of Glassy Azobenzene Polymers and Networks

    Science.gov (United States)

    Vaia, R. A.

    2013-03-01

    Continual innovation at the forefront of soft-matter, in areas such as liquid crystal networks, nano-composites and bio-molecules, is providing exciting opportunities to create smart materials systems that exhibit a controlled, reproducible and reversible modulation of physical properties. These material systems evoke the adaptivity of natural organisms, and inspire radical aerospace notions. A key example is photo-responsive polymers, which convert a light stimulus input into a mechanical output (work). Photoinduced conformational changes, such as within azobenzene, dictate molecular-level distortions that summate into a macroscopic strain, which often manifests as a shape change or motion. The transduction of the molecular-level response to a macroscale effect is regulated by mesoscopic features, such as chain packing, free volume, and local molecular order - factors which depend on chemical composition as well as the process history of the material. For example, physical aging increases the density of the glass, reduces local free volume, and thus decreases the minima in local conformation space which strongly influences the azobenzene photochemistry (trans-cis-trans isomerization). The subsequent change in the energy landscape of the system reduces the fraction of azobenzene able to undergo reconfiguration as well as increases the probability that those photoinduced conformations will relax back to the initial local environment. The result is a tuning of the magnitude of macroscopic strain and the ability to shift from shape fixing to shape recovery, respectively. Work done in collaboration with H. Koerner, K.M. Lee, M. Smith, D. Wang, L-S. Tan. and T. White, Air Force Research Laboratory.

  4. Comparison Between the Elasticity of Polyacrylamide and Polyacrylic Gels

    OpenAIRE

    Benguigui, L.

    1995-01-01

    We measured the Young modulus E of polyacrylamide and polyacrylic gels as a function of the crosslink and polymer concentrations. We found that the variation of E with these two parameters is completely different for the two kinds of gels. For the polyacrylic gels, E is an increasing function of the crosslink and polymer concentrations. However, in the case of the polyacrylamide gels, E increases with polymer concentration but not always with the crosslink concentration. For low polymer conce...

  5. Novel Nanocomposite Optical Plastics: Dispersion of Titanium in Polyacrylates

    OpenAIRE

    Gunjan Suri; Mukti Tyagi; Geetha Seshadri; Gurcharan Lal Verma; Rakesh Kumar Khandal

    2010-01-01

    Polyacrylates have become the preferred materials for optical applications replacing the conventionally used glass due to their superior optical clarity. The major disadvantage with polyacrylates is their low (1.40–1.50) refractive index besides their poor impact resistance. The improvements in refractive index as well as mechanical properties can be achieved by way of incorporation of metals or metal compounds in the matrix. A novel methodology for the incorporation of high refractive index ...

  6. Antitumor activity of polyacrylates of noble metals in experiment

    OpenAIRE

    Larisa A. Ostrovskaya; David B. Korman; Natalia V. Bluhterova; Margarita M. Fomina; Valentina A. Rikova; Claudia A. Abzaeva; Larisa V. Zhilitskaya; Nina O. Yarosh

    2014-01-01

    The aim of this research has been the study of the antitumor activity of polymetalacrylate derivatives containing in their structure noble metals. Metallic derivatives of polyacrylic acid were not previously tested as antitumor agents.The antitumor activity of polyacrylates, containing argentum (argacryl), aurum (auracryl) and platinum (platacryl) against experimental models of murine solid tumors (Lewis lung carcinoma and Acatol adenocarcinoma) as well as acute toxicity have been studied. It...

  7. Electrosynthesis of polyacrylic/polypyrrole composites : formation of polypyrrole wires

    OpenAIRE

    Jérôme, Christine; Labaye, David; Bodart, Isabelle; Jérôme, Robert

    1999-01-01

    A new preparation method is reported for the synthesis of conducting polypyrrole nanowires. This two-step all-electrochemical method consists in the cathodic grafting of a thin polyacrylate film on a carbon electrode, which is then used as an anode for the electropolymerization of pyrrole. Scanning electron microscopy shows the formation of polypyrrole wires (diameter ~600 nm lenght ~300 µm) growing through holes in the polyacrylate precoating. The effect of the experimental conditions, such ...

  8. Intramolecular photoinduced electron-transfer in azobenzene-perylene diimide

    International Nuclear Information System (INIS)

    This paper studies the intramolecular photoinduced electron-transfer (PET) of covalent bonded azobenzene-perylene diimide (AZO-PDI) in solvents by using steady-state and time-resolved fluorescence spectroscopy together with ultrafast transient absorption spectroscopic techniques. Fast fluorescence quenching is observed when AZO-PDI is excited at characteristic wavelengths of AZO and perylene moieties. Reductive electron-transfer with transfer rate faster than 1011 s−1 is found. This PET process is also consolidated by femtosecond transient absorption spectra

  9. Attraction or Repulsion? London Dispersion Forces Control Azobenzene Switches.

    Science.gov (United States)

    Schweighauser, Luca; Strauss, Marcel A; Bellotto, Silvia; Wegner, Hermann A

    2015-11-01

    Large substituents are commonly seen as entirely repulsive through steric hindrance. Such groups have additional attractive effects arising from weak London dispersion forces between the neutral atoms. Steric interactions are recognized to have a strong influence on isomerization processes, such as in azobenzene-based molecular switches. Textbooks indicate that steric hindrance destabilizes the Z isomers. Herein, we demonstrate that increasing the bulkiness of electronically equal substituents in the meta-position decreases the thermal reaction rates from the Z to the E isomers. DFT computations revealed that attractive dispersion forces essentially lower the energy of the Z isomers. PMID:26350759

  10. Photoresponsive Block Copolymers Containing Azobenzenes and Other Chromophores

    Directory of Open Access Journals (Sweden)

    Takaomi Kobayashi

    2010-01-01

    Full Text Available Photoresponsive block copolymers (PRBCs containing azobenzenes and other chromophores can be easily prepared by controlled polymerization. Their photoresponsive behaviors are generally based on photoisomerization, photocrosslinking, photoalignment and photoinduced cooperative motions. When the photoactive block forms mesogenic phases upon microphase separation of PRBCs, supramolecular cooperative motion in liquid-crystalline PRBCs enables them to self-organize into hierarchical structures with photoresponsive features. This offers novel opportunities to photocontrol microphase-separated nanostructures of well-defined PRBCs and extends their diverse applications in holograms, nanotemplates, photodeformed devices and microporous films.

  11. Controlled swelling and adsorption properties of polyacrylate/montmorillonite composites

    Energy Technology Data Exchange (ETDEWEB)

    Natkanski, Piotr [Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Krakow (Poland); Kustrowski, Piotr, E-mail: kustrows@chemia.uj.edu.pl [Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Krakow (Poland); Bialas, Anna; Piwowarska, Zofia [Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Krakow (Poland); Michalik, Marek [Institute of Geological Sciences, Jagiellonian University, Oleandry 2a, 30-063 Krakow (Poland)

    2012-10-15

    A series of novel polyacrylate/montmorillonite composites was synthesized by in situ polymerization in aqueous slurry of clay. Dissociated (obtained by adding ammonium or sodium hydroxide) and undissociated forms of acrylic acid were used as monomers in the hydrogel synthesis. The structure and composition of the samples were studied by powder X-ray diffraction, diffuse reflectance infra-red Fourier transform spectroscopy, thermogravimetry and elemental analysis. It has been found that the kind of monomer influences strongly the location of a polymer chain in the formed composite. Complete intercalation of hydrogel into the interlayer space of montmorillonite was observed for sodium polyacrylate, whereas polyacrylic acid and ammonium polyacrylate mainly occupied the outer surface of the clay. The position of hydrogel determined the swelling and adsorption properties of the studied composites. The important factor influencing the kinetics of Fe(III) cation adsorption was pH. The analysis of adsorption isotherms allowed to propose the mechanism of Fe(III) cation adsorption. Highlights: Black-Right-Pointing-Pointer Polyacrylate hydrogels can be introduced into the interlayers of clay. Black-Right-Pointing-Pointer The position of hydrogel in the composite depends on the polymer type. Black-Right-Pointing-Pointer Ammonium polyacrylate places outside the clay, sodium one is intercalated into it. Black-Right-Pointing-Pointer Swelling and adsorption capacities can be controlled by the polymer position. Black-Right-Pointing-Pointer High adsorption efficiency in Fe(III) removal was observed.

  12. Layer-by-layer deposited organic/inorganic hybrid multilayer films containing noncentrosymmetrically orientated azobenzene chromophores.

    Science.gov (United States)

    Kang, En-Hua; Bu, Tianjia; Jin, Pengcheng; Sun, Junqi; Yang, Yanqiang; Shen, Jiacong

    2007-07-01

    Organic/inorganic hybrid multilayer films with noncentrosymmetrically orientated azobenzene chromophores were fabricated by the sequential deposition of ZrO2 layers by a surface sol-gel process and subsequent layer-by-layer (LbL) adsorption of the nonlinear optical (NLO)-active azobenzene-containing polyanion PAC-azoBNS and poly(diallyldimethylammonium chloride) (PDDA). Noncentrosymmetric orientation of the NLO-active azobenzene chromophores was achieved because of the strong repulsion between the negatively charged ZrO(2) and the sulfonate groups of the azobenzene chromophore in PAC-azoBNS. Regular deposition of ZrO(2)/PAC-azoBNS/PDDA multilayer films was verified by UV-vis absorption spectroscopy and quartz crystal microbalance measurements. Both UV-vis absorption spectroscopy and transmission second harmonic generation (SHG) measurements confirmed the noncentrosymmetric orientation of the azobenzene chromophores in the as-prepared ZrO2/PAC-azoBNS/PDDA multilayer films. The square root of the SHG signal (I(2omega)(1/2)) increases with the increase of the azobenzene graft ratio in PAC-azoBNS as the number of deposition cycles of the ZrO(2)/PAC-azoBNS/PDDA films remains the same, while the second-order susceptibility chi(zzz)(2) of the film decreases with the increase of the azobenzene graft ratio. Furthermore, the present method was successfully extended to realize the noncentrosymmetric orientation of azobenzene chromophores in multilayer films when small organic azobenzene compounds with carboxylic acid and/or hydroxyl groups at one end and sulfonate groups at the other end were used. The present method was characterized by its simplicity and flexibility in film preparation, and it is anticipated to be a facile way to fabricate second-order nonlinear optical film materials. PMID:17555337

  13. Structure dependence of photochromism and thermochromism of azobenzene-functionalized polythiophenes

    Directory of Open Access Journals (Sweden)

    2007-07-01

    Full Text Available Two novel azobenzene-functionalized polythiophenes, poly[4-((4-(phenylazophenoxybutyl-3-thienylacetate] (P4 and the copolymer of 3-hexylthiophene and 4-((4-(phenylazophenoxybutyl-3-thienylacetate (COP64 have been synthesized. The structure dependence of photoluminescence features and thermochromic behaviors of both azobenzene-functionalized polymers was investigated. The results show that polymer structure has a strong influence on the conformation and optical properties of the resulting polythiophene derivatives. The photochemical control of photoluminescence property was achieved with homopolymer P4 using photoactive azobenzene side chains.

  14. Photoisomerization dynamics of azobenzene materials for solar thermal fuels

    Science.gov (United States)

    Strubbe, David; Grossman, Jeffrey

    2013-03-01

    A solar thermal fuel absorbs sunlight and stores the energy chemically via an induced structural change, which can later be reversed to release the energy as heat. Azobenzene molecules have a cis-trans photoisomerization with these properties, and hydrogen-bonding and packing via attachment to rigid template structures have shown promise in increasing the energy stored and the length of time it can be stored [A Kolpak et al, Nano Lett. 11, 3156-3162 (2011)]. Other important factors in determining the efficiency of a solar thermal fuel are the absorption cross-section and the quantum yield for photoisomerization, which must also be optimized for a successful material. We employ time-dependent density-functional theory (TDDFT) and the GW/Bethe-Salpeter formalism to calculate the optical absorption and dynamics in the excited-state to address these two factors. We use excited-state forces to map out potential-energy surfaces and follow the structural change after absorption for azobenzene-derived materials, to correlate the efficiency of photoisomerization with the functionalization and template.

  15. Synthesis and Properties of 2'-Deoxyuridine Analogues Bearing Various Azobenzene Derivatives at the C5 Position

    Directory of Open Access Journals (Sweden)

    Shohei Mori

    2015-03-01

    Full Text Available Nucleic acids that change their properties upon photo-irradiation could be powerful materials for molecular sensing with high spatiotemporal resolution. Recently, we reported a photo-isomeric nucleoside bearing azobenzene at the C5 position of 2'-deoxyuridine (dUAz, whose hybridization ability could be reversibly controlled by the appropriate wavelength of light. In this paper, we synthesized and evaluated dUAz analogues that have various para-substitutions on the azobenzene moiety. Spectroscopic measurements and HPLC analyses revealed that the para-substitutions of the azobenzene moiety strongly affect the photo-isomerization ability and thermal stability of the cis-form. The results suggest that proper substitution of the azobenzene moiety can improve the properties of dUAz as a light-responsive nucleic acid probe.

  16. Studies of azobenzene-containing triazatriangulenium adlayers on Au(111) surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Jung, Ulrich; Kuhn, Sonja; Mueller, Mathias; Filinova, Olena; Baisch, Belinda; Magnussen, Olaf [Institut fuer Experimentelle und Angewandte Physik, Christian-Albrechts-Universitaet zu Kiel, Leibnizstrasse 19, 24118 Kiel (Germany); Kubitschke, Jens; Herges, Rainer [Otto-Diels-Institut fuer Organische Chemie, Christian-Albrechts-Universitaet zu Kiel, Otto-Hahn-Platz 3, 24098 Kiel (Germany)

    2010-07-01

    The attachment of molecular functions such as photoswitches to metal surfaces is of major interest in nanotechnology. One of the most frequently studied class of photoswitches are azobenzenes, which exhibit trans-cis isomerism. The typical method to attach azobenzene to surfaces is self-assembly of thiols on Au. However, in such adlayers the photoisomerization is often totally quenched because of steric effects. To overcome the problems of conventional azobenzene adlayers, we were employing a novel approach using customizable triazatriangulenium (TATA) platforms. Here, we present the structure and photoswitching properties of azobenzene-containing TATA adlayers on Au(111), obtained by structure-sensitive, spectroscopic, and electrochemical methods. Functionalized TATA molecules exhibit a strong tendency to form bilayers. We demonstrate, that it is possible to suppress bilayer formation and thus to form highly-ordered functionalized TATA monolayers. Furthermore, the photoswitching processes in these adlayers obey first order kinetics with quantum efficiencies of <10{sup -3}.

  17. Optical Modulation of the Diffraction Efficiency in an Indoline Azobenzene/Amorphous Polycarbonate Film.

    Science.gov (United States)

    Williams, G V M; Do, My T T; Middleton, A; Raymond, S G; Bhuiyan, M D H; Kay, A J

    2016-12-01

    We have made a diffraction grating in an indoline azobenzene/amorphous polycarbonate film by two-beam interference at 532 nm that periodically photodegrades the indoline azobenzene dye. Subsequent illumination of the film with 532-nm light into the trans-isomer band leads to trans-cis isomerization in the indoline azobenzene dye and results in a decrease in the trans-isomer band absorption coefficient. This causes the diffraction efficiency to decrease when probed at 655 nm. The diffraction efficiency returns to its original value when the 532-nm light is blocked by thermal relaxation from the indoline azobenzene cis-isomer to the trans-isomer. Thus, we have been able to optically modulate the diffraction efficiency in a thin film diffraction grating. PMID:27416904

  18. Theoretical Investigation of Nonlinear Optical Properties of Organic and Transition Metal Hybrid Azobenzene Dendrimers

    Institute of Scientific and Technical Information of China (English)

    LIU Cai-Ping; LIU Ping; WU Ke-Chen

    2008-01-01

    In this work, we report a theoretical exploration of the responses of organic azo-benzene dendrimers. The polarizabilities, the first and second hyperpolarizabilities of the azobenzene monomers (GO), and the first, second and third generation (G1, G2 and G3, respectively) are investigated by semi-empirical methods. The calculated results show that the nonlinear optical (NLO)properties of these organic dendrimers are mainly determined by the azobenzene chromospheres.Additionally, the values of β and γ increase almost in proportion to the number of chromophores. On the other hand, two types of transition metal hybrid azobenzene dendrimers (core-hybrid and branch-end hybrid according to the sites combined with transition metals) are simulated and discussed in detail in the framework of time-dependent density functional theory (TDDFT). The calculated results reveal that the NLO responses of these metal dendrimers distinctly varied as a result of altering the charge transfer transition scale and the excitation energies.

  19. Transformation mechanism of n-butyl terminated Si nanoparticles embedded into Si1-xCx nanocomposites mixed with Si nanoparticles and C atoms

    International Nuclear Information System (INIS)

    Bright-field transmission electron microscopy (TEM) images, high-resolution TEM (HRTEM) images, and fast-Fourier transformed electron-diffraction patterns showed that n-butyl terminated Si nanoparticles were aggregated. The formation of Si1-xCx nanocomposites was mixed with Si nanoparticles and C atoms embedded in a SiO2 layer due to the diffusion of C atoms from n-butyl termination shells into aggregated Si nanoparticles. Atomic force microscopy (AFM) images showed that the Si1-xCx nanocomposites mixed with Si nanoparticles and C atoms existed in almost all regions of the SiO2 layer. The formation mechanism of Si nanoparticles and the transformation mechanism of n-butyl terminated Si nanoparticles embedded into Si1-xCx nanocomposites mixed with Si nanoparticles and C atoms are described on the basis of the TEM, HRTEM, and AFM results. These results can help to improve the understanding of the formation mechanism of Si nanoparticles.

  20. Fabrication of silver nanoparticles embedded into polyvinyl alcohol (Ag/PVA) composite nanofibrous films through electrospinning for antibacterial and surface-enhanced Raman scattering (SERS) activities.

    Science.gov (United States)

    Zhang, Zhijie; Wu, Yunping; Wang, Zhihua; Zou, Xueyan; Zhao, Yanbao; Sun, Lei

    2016-12-01

    Silver nanoparticle-embedded polyvinyl alcohol (PVA) nanofibers were prepared through electrospinning technique, using as antimicrobial agents and surface-enhanced Raman scattering (SERS) substrates. Ag nanoparticles (NPs) were synthesized in liquid phase, followed by evenly dispersing in PVA solution. After electrospinning of the mixed solution at room temperature, the PVA embedded with Ag NPs (Ag/PVA) composite nanofibers were obtained. The morphologies and structures of the as-synthesized Ag nanoparticles and Ag/PVA fibers were characterized by the techniques of transmission electron microscopy (TEM), X-ray diffraction (XRD), ultraviolet-visible absorption spectroscopy (UV-vis), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). Ag NPs have an average diameter of 13.8nm, were found to be uniformly dispersed in PVA nanofibers. The Ag/PVA nanofibers provided robust antibacterial activities against both Gram-positive Staphylococcus aureus (S. aureus) and Gram-negative Escherichia coli (E. coli) microorganisms. It's also found that Ag/PVA nanofibers make a significant contribution to the high sensitivity of SERS to 4-mercaptophenol (4-MPh) molecules. PMID:27612736

  1. Enhanced oxygen sensing properties of Pt(II) complex and dye entrapped core-shell silica nanoparticles embedded in sol-gel matrix.

    Science.gov (United States)

    Chu, Chen-Shane; Lo, Yu-Lung; Sung, Ti-Wen

    2010-08-15

    This paper presents a highly sensitive oxygen sensor that comprises an optical fiber coated at one end with platinum(II) meso-tetrakis(pentafluorophenyl)porphyrin (PtTFPP) and PtTFPP entrapped core-shell silica nanoparticles embedded in an n-octyltriethoxysilane (Octyl-triEOS)/tetraethylorthosilane (TEOS) composite xerogel. The sensitivity of the optical oxygen sensor is quantified in terms of the ratio I(0)/I(100), where I(0) and I(100) represent the detected fluorescence intensities in pure nitrogen and pure oxygen environments, respectively. The experimental results show that the oxygen sensor has a sensitivity (I(0)/I(100)) of 166. The response time was 1.3s when switching from pure nitrogen to pure oxygen, and 18.6s when switching in the reverse direction. The experimental results show that compared to oxygen sensors based on PtTFPP, PtOEP, or Ru(dpp)(3)(2+) dyes, the proposed optical fiber oxygen sensor has the highest sensitivity. In addition to the increased surface area per unit mass of the sensing surface, the dye entrapped in the core of silica nanoparticles also increases the sensitivity because a substantial number of aerial oxygen molecules penetrate the porous silica shell. The dye entrapped core-shell nanoparticles is more prone to oxygen quenching. PMID:20678666

  2. Nonvolatile flexible organic bistable devices fabricated utilizing CdSe/ZnS nanoparticles embedded in a conducting poly N-vinylcarbazole polymer layer

    International Nuclear Information System (INIS)

    The bistable effects of CdSe/ZnS nanoparticles embedded in a conducting poly N-vinylcarbazole (PVK) polymer layer by using flexible poly-vinylidene difluoride (PVDF) and polyethylene terephthalate (PET) substrates were investigated. Transmission electron microscopy (TEM) images revealed that CdSe/ZnS nanoparticles were formed inside the PVK polymer layer. Current-voltage (I-V) measurement on the Al/[CdSe/ZnS nanoparticles+ PVK]/ITO/PVDF and Al/[CdSe/ZnS nanoparticles+ PVK ]/ITO/PET structures at 300 K showed a nonvolatile electrical bistability behavior with a flat-band voltage shift due to the existence of the CdSe/ZnS nanoparticles, indicative of trapping, storing and emission of charges in the electronic states of the CdSe nanoparticles. A bistable behavior for the fabricated organic bistable device (OBD) structures is described on the basis of the I-V results. These results indicate that OBDs fabricated by embedding inorganic CdSe/ZnS nanoparticles in a conducting polymer matrix on flexible substrates are prospects for potential applications in flexible nonvolatile flash memory devices

  3. Induction of molecular chirality by circularly polarized light in cyclic azobenzene with a photoswitchable benzene rotor.

    Science.gov (United States)

    Hashim, P K; Thomas, Reji; Tamaoki, Nobuyuki

    2011-06-20

    New phototriggered molecular machines based on cyclic azobenzene were synthesized in which a 2,5-dimethoxy, 2,5-dimethyl, 2,5-difluorine or unsubstituted-1,4-dioxybenzene rotating unit and a photoisomerizable 3,3'-dioxyazobenzene moiety are bridged together by fixed bismethylene spacers. Depending upon substitution on the benzene moiety and on the E/Z conformation of the azobenzene unit, these molecules suffer various degrees of restriction on the free rotation of the benzene rotor. The rotation of the substituted benzene rotor within the cyclic azobenzene cavity imparts planar chirality to the molecules. Cyclic azobenzene 1, with methoxy groups at both the 2- and 5-positions of the benzene rotor, was so conformationally restricted that free rotation of the rotor was prevented in both the E and Z isomers and the respective planar chiral enantiomers were resolved. In contrast, compound 2, with 2,5-dimethylbenzene as the rotor, demonstrated the property of a light-controlled molecular brake, whereby rotation of the 2,5-dimethylbenzene moiety is completely stopped in the E isomer (brake ON, rotation OFF), while the rotation is allowed in the Z isomer (brake OFF, rotation ON). The cyclic azobenzene 3, with fluorine substitution on the benzene rotor, was in the brake OFF state regardless of E/Z photoisomerization of the azobenzene moiety. More interestingly, for the first time, we demonstrated the induction of molecular chirality in a simple monocyclic azobenzene by circular-polarized light. The key characteristics of cyclic azobenzene 2, that is, stability of the chiral structure in the E isomer, fast racemization in the Z isomer, and the circular dichroism of enantiomers of both E and Z isomers, resulted in a simple reversible enantio-differentiating photoisomerization directly between the E enantiomers. Upon exposure to r- or l-circularly polarized light at 488 nm, partial enrichment of the (S)- or (R)-enantiomers of 2 was observed. PMID:21567494

  4. Self-Driven Bioelectrochemical Mineralization of Azobenzene by Coupling Cathodic Reduction with Anodic Intermediate Oxidation

    International Nuclear Information System (INIS)

    Highlights: • Azobenzene was reduced to aniline at the cathode of an acetate-fueled MFC. • Aniline was degraded at the bioanode of a single-chamber MFC. • Cathodic reduction of azobenzene was coupled with anodic oxidation of aniline. • Self-driven, complete mineralization of azobenzene in an MFC was accomplished. - Abstract: Bioelectrochemical systems have been intensively studied as a promising technology for wastewater treatment and environment remediation. Coupling of the anodic and cathodic electrochemical reactions allows an enhanced degradation of recalcitrant organics, but external power supply is usually needed to overcome the thermodynamic barrier. In this work, we report a self-driven degradation of azobenzene in a microbial fuel cell (MFC), where the cathodic reduction of azobenzene was effectively coupled with the anodic oxidation of its reduction degradation intermediate (i.e., aniline). The anodic degradation rate of aniline, as the sole carbon source, was significantly higher than that under open-circuit conditions, suggesting a considerable bioelectrochemical oxidation of aniline. Output voltages up to 8 mV were obtained in the MFC. However, a shift of cathodic electron acceptor from oxygen to azobenzene resulted in a decreased aniline degradation rate and output voltage. The present work may provide valuable implications for development of sustainable bioelectrochemical technologies for environmental remediation

  5. Light scattering of thin azobenzene side-chain polyester layers

    DEFF Research Database (Denmark)

    Kerekes, Á.; Lörincz, E.; Ramanujam, P.S.;

    2002-01-01

    Light scattering properties of liquid crystalline and amorphous azobenzene side-chain polyester layers used for optical data storage were examined by means of transmissive scatterometry. Comparative experiments show that the amorphous polyester has significantly lower light scattering...... characteristics than the liquid crystalline polyester. The amorphous samples have negligible polarization part orthogonal to the incident beam. the liquid crystalline samples have relative high orthogonal polarization part in light scattering, The light scattering results can be used to give a lower limit for the...... domain size in thin liquid crystalline polyester layers being responsible for the dominant light scattering. The characteristic domain Sizes obtained from the Fourier transformation of polarization microscopic Pictures confirm these values....

  6. Polymer scaffolds bearing azobenzene - Potential for optical information storage

    DEFF Research Database (Denmark)

    Hvilsted, Søren; Ramanujam, P.S.

    2001-01-01

    The fundamental optical storage mechanism of the laser light addressable azobenzene moiety is briefly introduced. A modular and flexible synthesis design furnishes polyester matrices covalently integrating cyanoazobenzene in regularly spaced side chains. Thin films of these materials are...... particularly well suited for holographic storage. Notable figures of merits of liquid crystalline polyesters are response time to blue-green laser light of the order of nanoseconds, storage capacity expressed as 5000 lines/mm, and high, permanent (almost nine years) diffraction efficiency of the order of 50......% or greater, and erasability. The implications of the main chain nature for polyester morphology and for the permanency of the induced anisotropy are discussed. The design and methods of preparation of other significantly different polymer scaffolds supporting cyanoazobenzene are elaborated...

  7. Photomechanical Bending of Azobenzene-Based Photochromic Molecular Fibers

    Directory of Open Access Journals (Sweden)

    Riku Matsui

    2013-03-01

    Full Text Available Microfibers composed of azobenzene-based photochromic amorphous molecular materials, namely low molecular-mass photochromic materials with a glass-forming property, could be fabricated. These fibers were found to exhibit mechanical bending motion upon irradiation with a laser beam. In addition, the bending direction could be controlled by altering the polarization direction of the irradiated light without changing the position of the light source or the wavelength of the light. In-situ fluorescence observation of mass transport induced at the surface of the fiber doped with CdSe quantum dots suggested that the bending motions were related with the photoinduced mass transport taking place near the irradiated surface of the fiber.

  8. Antimicrobial azobenzene compounds and their potential use in biomaterials

    Science.gov (United States)

    Sessa, L.; Concilio, S.; Iannelli, P.; De Santis, F.; Porta, A.; Piotto, S.

    2016-04-01

    We recently synthesized a class of active compounds with azobenzene structure [1] and lowest in silico toxicity values. The antimicrobial activity of these molecules and their thermal stability are very promising and indicate that they may have interesting and therapeutically significant applications. This work aims to develop new materials with antibacterial and antifungal activity inserting different percentages of synthetic antimicrobial azo compounds in commercial polymer matrices. We realized thin films using solvent casting and melt compounding techniques. The obtained materials retained the proprieties of the pure matrices. This means that azo dye dissolved in the matrix does not influence the thermal behavior and the morphology of the material. Tested films exhibited the capability to inhibit biofilms formation of S. aureus and C. albicans. Spectrophotometric investigation of the azo compound released from the polymer matrices confirmed that the realized materials might be interesting for biomedical tools, antibacterial surfaces, and films for active packaging.

  9. Antitumor activity of polyacrylates of noble metals in experiment

    Directory of Open Access Journals (Sweden)

    Larisa A. Ostrovskaya

    2014-08-01

    Full Text Available The aim of this research has been the study of the antitumor activity of polymetalacrylate derivatives containing in their structure noble metals. Metallic derivatives of polyacrylic acid were not previously tested as antitumor agents.The antitumor activity of polyacrylates, containing argentum (argacryl, aurum (auracryl and platinum (platacryl against experimental models of murine solid tumors (Lewis lung carcinoma and Acatol adenocarcinoma as well as acute toxicity have been studied. It is found that the polyacrylates of noble metals are able to inhibit tumor growth up to 50-90% in comparison with the control. Auracryl induced the inhibition of the Lewis lung carcinoma and Acatol adenocarcinoma by 80 and 90% in comparison with the control, results recommending it for further advanced preclinical studies.

  10. Glycosylated polyacrylate nanoparticles by emulsion polymerization.

    Science.gov (United States)

    Abeylath, Sampath C; Turos, Edward

    2007-08-01

    A selection of glycosylated polyacrylate nanoparticles has been prepared by radical-initiated emulsion polymerization in aqueous media. Using ethyl acrylate as a co-monomer, carbohydrate acrylates were incorporated into the poly(ethyl acrylate) framework to give stable emulsions of glyconanoparticles with an average particle size of around 40 nm. Using this technique a variety of glyconanoparticles were prepared from 3-O-acryloyl-1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranose, 1-O-acryloyl-2,3:5,6-di-O-isopropylidene-alpha-D-mannofuranose, 6-O-acryloyl-1,2:3,4-di-O-isopropylidene-alpha-D-galactopyranose, 2-N-acryloyl-1,3,4,6-tetra-O-acetyl-beta-D-glucosamine, 5-O-acryloyl-2,3-isopropylidene-1-methoxy-beta-D-ribofuranose and 4-N-acetyl-5'-O-acryloyl-2',3'-O-isopropylidene cytidine. Scanning electron microscopy, dynamic light scattering and proton NMR analysis of the emulsions indicated essentially 100% incorporation of the carbohydrate acrylate monomer into the polymer with the exception of O-benzyl- and O-benzoyl-protected carbohydrate acrylates, which gave incomplete incorporation. Formation of larger glyconanoparticles of ~80nm with (unprotected) 3-O-acryloyl-D-glucose and 5-O-acryloyl-1-methoxy-beta-D-ribofuranose revealed the influence of free hydroxyl groups in the monomer on the particle size during polymerization, a feature which is also apparently dependent on the amount of carbohydrate in the matrix. This methodology allows for a new, simple route to the synthesis of polymeric glyconanoparticles with potential applications in targeted drug delivery and materials development. PMID:18677404

  11. Novel Nanocomposite Optical Plastics: Dispersion of Titanium in Polyacrylates

    Directory of Open Access Journals (Sweden)

    Gunjan Suri

    2010-01-01

    Full Text Available Polyacrylates have become the preferred materials for optical applications replacing the conventionally used glass due to their superior optical clarity. The major disadvantage with polyacrylates is their low (1.40–1.50 refractive index besides their poor impact resistance. The improvements in refractive index as well as mechanical properties can be achieved by way of incorporation of metals or metal compounds in the matrix. A novel methodology for the incorporation of high refractive index metals into low refractive index polymeric materials to improve the refractive index and impact resistance of the latter has been developed. With the in-situ formation of nanoparticles of TiO2, the refractive index of polyacrylates improved from 1.45 to 1.53 and the Abbe number increased from 40 to 57. One of the interesting dimension of this study pertains to the possibility of tailor-making of the two key optical properties of materials by way of varying the amount of TiO2 being formed in-situ. Thermal stability and impact resistance of nano dispersed (4.3% by wt. of Ti polyacrylates are found to be better than the neat polyacrylates. Moreover, TiO2-containing polyacrylate is of light weight. TEM, SEM, and IR analysis confirms the in-situ formation of nanoparticles of TiO2. Gamma irradiation has been used as an eco-friendly technique for polymerization. The developed compositions can be cast polymerized into clear and bubble free material for optical applications.

  12. Physicochemical and structural studies of clathrate hydrates of tetrabutylammonium polyacrylates.

    Science.gov (United States)

    Terekhova, Irina S; Manakov, Andrey Yu; Komarov, Vladislav Yu; Villevald, Galina V; Burdin, Alexander A; Karpova, Tamara D; Aladko, Eugeny Ya

    2013-03-01

    In this work, physicochemical and structural studies have been carried out for semiclathrate hydrates of linear (un-cross-linked) and cross-linked tetrabutylammonium polyacrylates with different degrees of cross-linking of the polymeric guest molecules (n = 0.5, 1, 2, 3%) and different degrees of substitution of proton ions of carboxylic groups in poly(acrylic acid) for TBA cations (x = 1, 0.8, 0.6). The changes in the hydrates' stability and composition depending on the outlined parameters were examined in the course of phase diagram studies of the binary systems water-tetrabutylammonium polyacrylates using differential thermal analysis method and calorimetric measurements of fusion enthalpies of the hydrates. Phase diagram studies of the binary system water-linear tetrabutylammonium polyacrylate revealed the formation of four hydrates. Based on the data of chemical analysis of hydrate crystals the compositions of all hydrates have been determined. Single-crystal X-ray diffraction studies revealed a tetragonal structure, space group 4/m, and unit cell parameters are close for different hydrates and lie in the ranges a = 23.4289-23.4713 Å and c = 12.3280-12.3651 Å (150 K). The structure can be related to tetragonal structure I typical for the clathrate hydrates of tetraalkylammonium salts with monomeric anions. Powder X-ray diffraction analyses confirmed the identity of the above crystal structure to that of the hydrates with cross-linked tetrabutylammonium polyacrylates. The behavior of TBA polyacrylate hydrates under the pressure of methane was studied and quantitative assessment of the gas content in the hydrates was made using volumetric analysis method. PMID:23383955

  13. [Polyacrylates of noble metals as potential antitumor drugs].

    Science.gov (United States)

    Ostrovskaia, L A; Voronkov, M G; Korman, D B; Bliukhterova, N V; Fomina, M M; Rykova, V A; Abzaeva, K A; Zhilitskaia, L V

    2014-01-01

    The antitumor activity of polyacrylates of the noble metals containing argentum (argacryl), aurum (auracryl) and platinum (platacryl) has been studied using experimental murine solid tumor models (Lewis lung carcinoma and Acatol adenocarcinoma). It has been found that polyacrylates of the noble metals are capable of inhibiting tumor development by 50-90% compared to control. Auracryl that inhibites the growth of Lewis lung carcinoma and Acatol adenocarcinoma by 80 and 90%, respectively, compared to control is the most efficient among the tested compounds and can be recommended for the further profound preclinical studies. PMID:25707247

  14. Photodissociation UV-Vis Spectra of Cold Protonated Azobenzene and 4-(Dimethylamino)azobenzene and Their Benzenediazonium Cation Fragment.

    Science.gov (United States)

    Féraud, Géraldine; Dedonder-Lardeux, Claude; Jouvet, Christophe; Marceca, Ernesto

    2016-06-01

    Gas phase photodissociation electronic spectra of protonated azobenzene (ABH(+)) and 4-(dimethylamino)azobenzene (dmaABH(+)) were measured in a cryogenically cooled ion trap at temperatures of a few tens of Kelvin. Experimental results were complemented with electronic structure calculations in the ground state at the MP2/cc-pVDZ level of theory, and in the low lying excited states using the RI-CC2 method. Calculated energies revealed that only the trans isomers of the azonium molecular ions (protonation site on the azo group) will likely exist in the trap at the temperatures achieved in the experiment. The first transition of trans-ABH(+) is π* ← π, and the absorption band in the spectrum appears strongly red-shifted from that of the neutral molecule. The calculations showed that upon excitation the quasi-planar ground state (S0) transforms into a chairlike excited state (S1) by twisting the CNNC dihedral angle about 96°. A 41 cm(-1) active vibrational progression found in the ABH(+) spectrum may be associated with the twisting of the azo bond. Conversely, the electronic spectrum of dmaABH(+) exhibits a steep and unstructured S1 ← S0 absorption corresponding to a less distorted S1 state. The next two quasi-degenerate bands in the ABH(+) spectrum evidence sharper onsets and a charge transfer character. Using a second fragmentation laser and an additional He cooling pulse in the trap, it was possible to measure the UV spectrum of cold benzenediazonium fragments. PMID:27216229

  15. Effect of heat treatment on optical, dielectric and mechanical properties of silver nanoparticle embedded CaO-CaF2-P2O5 glass

    International Nuclear Information System (INIS)

    Highlights: • Silver nanoparticle embedded glass were synthesized using melt quenching technique. • Red shift in the SPR peak position indicates increase in size of the nanoparticle. • Ag nanoparticle size was estimated using TEM and XRD analysis. • Enhancement in the dielectric and mechanical properties was observed. - Abstract: Silver nanoparticle have been embedded in CaO-CaF2-P2O5 glass using melt quenching technique. The quenched glasses were heat treated at 550 °C for 10, 20, 30, 40 and 50 h. The growth of silver nanoparticle in the glass matrix appeared to be time dependent. FTIR spectra show that silver nanoparticle formation has not affected the vibration bands of basic phosphate tetrahedral network. The increase in compactness of the glass structure is confirmed by increase in measured density of the glasses with increase in the duration of the heat treatment. Glass containing spherical silver nanoparticle shows the red shift and increase in the full width half maxima (FWHM) of the surface plasmon resonance (SPR) in the visible region with increase in the duration of the heat treatment. X-ray diffraction pattern indicated the presence of Ag crystalline peaks along with amorphous structure on heat treating at 550 °C for 50 h. For the glass samples, the increase in dielectric constant and low dielectric loss around 0.005 were observed with increase in duration of the heat treatment. Both Vickers hardness and fracture toughness increased while the brittleness decreased which can be attributed to the increase in size of the nanoparticles in glass matrix

  16. Spontaneous gradual accumulation of hexagonally-aligned nano-silica on gold nanoparticles embedded in stabilized zirconia: a pathway from catalytic to NH3-sensing performance

    Science.gov (United States)

    Plashnitsa, Vladimir V.; Elumalai, Perumal; Fujio, Yuki; Kawaguchi, Toshikazu; Miura, Norio

    2011-05-01

    The present study highlights the influence of nano-impurities on the catalytic/sensing performance of nano-structured Au sensing-electrodes (SEs) housed in a quartz reactor and operated at high temperature over a long period of time. The planar sensor, made from a nano-structured Au-SE on a polished-polycrystalline (pp) yttria-stabilized zirconia (YSZ) substrate exhibited initially negligible electromotive force (emf) response to each of the examined gases (CO, CH4, C3H8, C3H6, NOx and NH3; 400 ppm each) at 700 °C in the presence of 5 vol.% oxygen and 5 vol.% water vapor. Such a poor emf response was attributed to the excellent gas-phase oxidation/reduction ability of Au nanoparticles embedded in the YSZ substrate at high temperature. The response of the planar sensor made up of nano-structured Au-SE was monitored for about 75 days at 700 °C. As a result of this long-term monitoring, we detected the appearance of highly sensitive and selective NH3 gas-sensing properties after 45-75 days of sensor operation. Detailed observation of the morphology and composition of the as-fabricated nano-structured Au-SE after 75 days operation at 700 °C revealed the gradual accumulation of hexagonally-aligned SiO2 nano-impurities on the surface of the Au nanoparticles. The NH3 sensing mechanism of the YSZ-based sensor using the spontaneously-formed composite (nano-Au + nano-SiO2)-SE is therefore proposed to be based on a strong acid-base interaction between gaseous NH3 and SiO2 nano-impurities, followed by spillover of adsorbed NH3 towards the nano-Au/pp-YSZ interface.

  17. 10,000 optical write, read, and erase cycles in an azobenzene sidechain liquid-crystalline polyester

    DEFF Research Database (Denmark)

    Holme, NCR; Ramanujam, P.S.; Hvilsted, Søren

    1996-01-01

    light from a krypton laser at 351 nm. The efficiency of the system shows several exponential decays, presumably associated ci with the azobenzene chromophores' aligning out of the plane of the film and the lifetime of the cis state of the azobenzene. A local temperature increase may also play a role...

  18. Preparation and icephobic properties of polymethyltrifluoropropylsiloxane–polyacrylate block copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Li, Xiaohui; Zhao, Yunhui [School of Materials Science and Engineering, and Tianjin Key Laboratory of Composite and Functional Materials, Tianjin University, Tianjin 300072 (China); Li, Hui [School of Chemistry and Chemical Engineering, Shandong Key Laboratory of Fluorine Chemistry and Chemical Engineering Materials, University of Jinan, Jinan 250022 (China); Yuan, Xiaoyan, E-mail: xyuan28@yahoo.com [School of Materials Science and Engineering, and Tianjin Key Laboratory of Composite and Functional Materials, Tianjin University, Tianjin 300072 (China)

    2014-10-15

    Highlights: • PMTFPS–b-polyacrylate copolymers in five different compositions were synthesized. • Enrichment of PMTFPS amounts at the surface made high F/Si value. • Icing delay time was related to the surface roughness. • Ice shear strength was decreased by the synergistic effect of silicone and fluorine. - Abstract: Five polymethyltrifluoropropylsiloxane (PMTFPS)–polyacrylate block copolymers (PMTFPS–b-polyacrylate) were synthesized by free radical polymerization of methyl methacrylate, n-butyl acrylate and hydroxyethyl methacrylate using PMTFPS macroazoinitiator (PMTFPS-MAI) in range of 10–50 mass percentages. The morphology, surface chemical composition and wettability of the prepared copolymer films were investigated by transmission electron microscopy, atomic force microscopy, X-ray photoelectron spectroscopy, and water contact angle measurement. Delayed icing time and ice shear strength of the films were also detected for the icephobic purpose. The surface morphologies of the copolymers were different from those of the bulk because of the migration of the PMTFPS segments to the air interface during the film formation. Maximal delayed icing time (186 s at −15 °C) and reduction of the ice shear strength (301 ± 10 kPa) which was significantly lower than that of polyacrylates (804 ± 37 kPa) were achieved when the content of PMTFPS-MAI was 20 wt%. The icephobicity of the copolymers was attributed primarily to the enrichment of PMTFPS on the film surface and synergistic effect of both silicone and fluorine. Thus, the results show that the PMTFPS–b-polyacrylate copolymer can be used as icephobic coating materials potentially.

  19. Optically switchable multi-stopband of non-quarter-wavelength dielectric multilayer using azobenzene polymer liquid crystal

    Science.gov (United States)

    Ozaki, Ryotaro; Kadowaki, Kazunori; Hagio, Takashi; Yagi, Ryohei; Kuwahara, Yutaka; Kurihara, Seiji

    2015-09-01

    Non-quarter-wave stacked dielectric multilayers including azobenzene polymer liquid crystal layers are investigated in this study. The azobenzene polymer liquid crystal has a photoinduced reversible refractive index based on photoisomerization. By using the reversible refractive-index change, the reflectance of a stopband can be controlled. In this system, the azobenzene molecules change their conformation when they are irradiated with ultraviolet (UV) or visible light. In general, stacking many layers of different thicknesses can produce broadband or multicolor reflections for a dielectric multilayer. However, in a multilayer having thick azobenzene layers, UV or visible light used for controlling photoisomerization hardly reaches the bottom part of the multilayer because the light is mainly absorbed at its top surface. To solve this problem, the dependence on the thickness ratio of the multilayer is investigated and a non-quarter-wave stacked multilayer having RGB reflections is experimentally demonstrated using thin azobenzene layers.

  20. Local Density Fluctuations Predict Photoisomerization Quantum Yield of Azobenzene-Modified DNA.

    Science.gov (United States)

    Kingsland, Addie; Samai, Soumyadyuti; Yan, Yunqi; Ginger, David S; Maibaum, Lutz

    2016-08-01

    Azobenzene incorporated into DNA has a photoisomerization quantum yield that depends on the DNA sequence near the azobenzene attachment site. We use Molecular Dynamics computer simulations to elucidate which physical properties of the modified DNA determine the quantum yield. We show for a wide range of DNA sequences that the photoisomerization quantum yield is strongly correlated with the variance of the number of atoms in close proximity to the outer phenyl ring of the azobenzene group. We infer that quantum yield is controlled by the availability of fluctuations that enable the conformational change. We demonstrate that these simulations can be used as a qualitative predictive tool by calculating the quantum yield for several novel DNA sequences, and confirming these predictions using UV-vis spectroscopy. Our results will be useful for the development of a wide range of applications of photoresponsive DNA nanotechnology. PMID:27428569

  1. Photoisomerization of azobenzene containing self-assembled monolayers investigated by Kelvin probe work function measurements

    International Nuclear Information System (INIS)

    Photoisomerization of asymmetric azobenzene disulfide self-assembled monolayer (SAM) on gold was characterized by the Kelvin probe work function measurements in ambient atmosphere. The reversible changes in work function between trans and cis azobenzene SAMs are reasonably interpreted by the molecular dipole moments normal to the surface based on the molecular conformational models. The different para-substituents of azobenzene with electron donating and electron-withdrawing properties induce opposite responses in work function against UV-vis photoirradiation, which is a direct evidence of functional SAMs being effective for the energy-level alignment at the organic/electrode interface. The Kelvin probe measurements in atmosphere eventually provide the work function value equivalent to that determined by ultraviolet photoelectron spectroscopy (UPS) in ultrahigh vacuum in our previous study.

  2. Colorimetric response of azobenzene-terminated polydiacetylene vesicles under thermal and photic stimuli

    Science.gov (United States)

    You, Xian; Chen, Xin; Zou, Gang; Su, Wei; Zhang, Qijin; He, Pingsheng

    2009-11-01

    We study the colorimetric reversibility of pure polymerized p-nitro azobenzene moiety-substituted diacetylene (PNADA) and PNADA/polymerized 10,12-pentacosadiynoic acid (PDA) complex vesicles under thermal and photic stimuli. Because of the strong intermolecular interaction among azobenzene mesogens within the vesicles, PNADA vesicles show enhanced stability and completely reversible thermochromic response. Polydiacetylene based complex vesicles with partial reversible chromatic properties under both thermal and photonic stimuli were reported for the first time, which provided a novel model system for the understanding of the chromatic transition mechanism of polydiacetylene materials.

  3. Determination of the Response Time of Photoanisotropy in Azobenzene Side-Chain Polyesters

    DEFF Research Database (Denmark)

    Bublitz, D.; Fleck, B.; Wenke, L.; Ramanujam, P. S.; Ramanujam, P.S.; Hvilsted, Søren

    We present a method which allows the determination of the response time to polarized light of an azobenzene side-chain polyester. This method is based on the measurement of intensities in dependence on the delay time between a pump and a probe pulse. The described method does not need a very...... sophisticated time resolving measuring equipment. The time resolution is in the order 10 ps and is comparable with the laser pulse duration. The response time of the azobenzene side-chain polyester E1aP has determined to be about 40 ps. (C) 2000 Elsevier Science B.V. All rights reserved....

  4. Modulational instability of incoherently coupled beams in azobenzene-containing polymer with photoisomerization nonlinearity

    Institute of Scientific and Technical Information of China (English)

    Zhang Bing-Zhi; Cui Hu; She Wei-Long

    2009-01-01

    The modulational instability of two incoherently coupled beams in azobenzene-containing polymer with photoisomerization nonlinearity is investigated analytically and numerically. Our results show that as a precursor to spatial optical soliton formation, modulational instability can be adjusted and controlled by the wavelength combinations of the signal and background beams. We also discuss the dependences of strength of modulational instability on intensities of two signal beams and background beam. These findings make it possible to predict the formation of incoherently coupled soliton pairs in azobenzene-containing polymer.

  5. Effect of heat and film thickness on a photoinduced phase transition in azobenzene liquid crystalline polyesters

    DEFF Research Database (Denmark)

    Sanchez, C; Alcala, R; Hvilsted, Søren;

    2003-01-01

    The liquid crystal to isotropic phase transition induced with 488 nm light in films of liquid crystalline azobenzene polyesters has been studied as a function of temperature, light intensity, and film thickness. That phase transition is associated with the photoinduced trans-cis-trans isomerizati......The liquid crystal to isotropic phase transition induced with 488 nm light in films of liquid crystalline azobenzene polyesters has been studied as a function of temperature, light intensity, and film thickness. That phase transition is associated with the photoinduced trans...

  6. Modulational instability of incoherently coupled beams in azobenzene-containing polymer with photoisomerization nonlinearity

    International Nuclear Information System (INIS)

    The modulational instability of two incoherently coupled beams in azobenzene-containing polymer with photoisomerization nonlinearity is investigated analytically and numerically. Our results show that as a precursor to spatial optical soliton formation, modulational instability can be adjusted and controlled by the wavelength combinations of the signal and background beams. We also discuss the dependences of strength of modulational instability on intensities of two signal beams and background beam. These findings make it possible to predict the formation of incoherently coupled soliton pairs in azobenzene-containing polymer. (classical areas of phenomenology)

  7. Interaction of neptunium(V) with polyacrylic acid

    International Nuclear Information System (INIS)

    For the quantitative description of the interaction of actinoids with humic substances, it is necessary to clarify the effects of both polyelectrolyte and heterogeneous nature of humic substances. To estimate these effects separately, polyacrylic acid has been selected as representative of well-defined, homogenous polymeric weak acids, and its interaction with Np(V) has been investigated by a solvent extraction method. By expressing the effective concentration of the complexing ligand by the concentration of ionized carboxylate groups, the apparent complex formation constant has been obtained at several pH, ionic strength and average molecular weights. The results indicated that the apparent complex formation constant varied with the degree of ionization(α) of polyacrylic acid and that the manner of variation resembled that of its apparent proton association constant. (author)

  8. Synthesis of Polyacrylate/Polysiloxane Copolymer and Its Damping Performance

    Institute of Scientific and Technical Information of China (English)

    夏宇正; 石淑先; 焦书科; 李素青

    2003-01-01

    The copolymer of polyacrylate/polysiloxane for vibration damping materials was synthesized through emulsion polymerization. The effects of the amount of methyl methacrylate (MMA),polysiloxane containing vinyl, initiator and emulsifier on the conversion, stability of polyacrylate/polysiloxane emulsion were discussed when the emulsion was prepared by pre-emulsifying half continuous method. The graft copolymer has good vibration damping performance. The widest glass transition region of the copolymer spans 100℃, and the highest value of tanδ reached 2.0. The glass transition of the samples was examined by dynamic mechanical analysis (DMA). The vibration damping performance of the graft copolymer was affected by the amount of poly-vinyl dimethylsiloxane (PVMS).

  9. Rheological Characterization of Cataplasm Bases Composed of Cross-Linked Partially Neutralized Polyacrylate Hydrogel

    OpenAIRE

    Wang, Jian; Zhang, Hongqin; An, Dianyun; Yu, Jian; Li, Wei; Shen, Teng; Wang, Jianxin

    2014-01-01

    Viscoelasticity is a useful parameter for characterizing the intrinsic properties of the cross-linked polyacrylate hydrogel used in cataplasm bases. The aim of this study was to investigate the effects of various formulation parameters on the rheological characteristics of polyacrylate hydrogel. The hydrogel layers were formed using a partially neutralized polyacrylate (Viscomate™), which contained acrylic acid and sodium acrylate in different copolymerization ratios, as the cross-linked gel ...

  10. Induction of mesenchymal stem cell chondrogenesis by polyacrylate substrates

    OpenAIRE

    Glennon-Alty, Laurence; Williams, Rachel; Dixon, Simon; Murray, Patricia

    2013-01-01

    Mesenchymal stem cells (MSCs) can generate chondrocytes in vitro, but typically need to be cultured as aggregates in the presence of transforming growth factor beta (TGF-β), which makes scale-up difficult. Here we investigated if polyacrylate substrates modelled on the functional group composition and distribution of the Arg-Gly-Asp (RGD) integrin-binding site could induce MSCs to undergo chondrogenesis in the absence of exogenous TGF-β. Within a few days of culture on the biomimetic polyacry...

  11. Obtaining polyacrylic acid labelled with tritium and deuterium

    International Nuclear Information System (INIS)

    The polyacrylic hydrogels are a technological alternative for the storage of tritium liquid wastes with low and intermediate activity. β radiation emitted by tritium produces destructive radiolytic processes in the polymer networks. These processes can be studied by radiometric techniques using radioisotope labelled compounds or by spectrophotometrical methods by determining the spectral isotopic effects in the IR range. In this work, a method of preparation of polyacrylic acid labelled with tritium (T) and deuterium (D) in α) - positions is presented. The α - T polyacrylic acid has been obtained by radiopolymerization of 30% aqueous solution of acrylic acid which contains α-T sodium acrylate as tracer. The activity concentration was 1mCi/ml. The deuterium labelled polymer was obtained by radiopolymerization of 30% aqueous solution of α - D acrylic acid with an absorbed dose rate of 0.3 Mrad/h from a 60Co γ source. The integral absorbed dose was 0.4 Mrad at room temperature. The labelled monomers were synthesized by heterogeneous catalytic hydrogenation (Pd/C catalyst) of αBr acrylic acid in the presence of Cu 2+ ions as homopolymerization inhibitors. The brominated compound was obtained by reaction of addition of Br2 to the acrylic acid in chloroform solution. (authors)

  12. Triphenyl group containing molecular glasses of azobenzene for photonic applications

    Science.gov (United States)

    Zarins, Elmars; Tokmakovs, Andrejs; Kokars, Valdis; Ozols, Andris; Augustovs, Peteris; Rutkis, Martins

    2016-03-01

    D-π-A type organic molecules have attracted considerable attention of scientists due to their potential applications in nonlinear optics and holographic data storage as light, flexible and low-cost photonic materials. To provide a better understanding on the relation between the compound chemical structure and their physical properties necessary for the mentioned purposes, eight glassy triphenyl group containing derivatives of azobenzene with incorporated 5,5-dimethylcyclohex-2-enylidene or 4H-pyran-4-ylidene structural fragments and dicyanomethylene, indene-1,3-dione and pyrimidine-2,4,6(1H,3H,5H)-trione acceptor groups have been synthesized and investigated. Thermal stability of synthesized glasses is no lower than 250 °C and glass transition in higher than 70 °C which both further increases (up to 120 °C) by additional number of attached triphenyl-moieties and incorporated structural fragments. Almost all of the synthesized azodyes form good optical quality transparent amorphous films from volatile organic solvents with their light absorption in thin solid films in the range of 400-660 nm. Azocompounds with sterically small cyclohex-2-ene-1-ylidene fragment in their molecules proved to be most efficient materials for holographic data storage and nonlinear optics with diffraction efficiency up to 20.40%, self diffraction efficiency up to 12.94% and NLO coefficient d33 up to 125.7 pm/V. Azodyes with no additionally incorporated structural fragments and indene-1,3-dione electron acceptor group were least efficient materials for these purposes, however may show potential as photoactive components in organic solar cells due to their remarkable light absorption properties in the solid state.

  13. Photosensitive response of azobenzene containing films towards pure intensity or polarization interference patterns

    Energy Technology Data Exchange (ETDEWEB)

    Yadavalli, Nataraja Sekhar; Santer, Svetlana, E-mail: santer@uni-potsdam.de [Department of Experimental Physics, Institute of Physics and Astronomy, University of Potsdam, 14476 Potsdam (Germany); Saphiannikova, Marina [Leibniz Institute of Polymer Research Dresden, 01069 Dresden (Germany)

    2014-08-04

    In this paper, we report on differences in the response of photosensitive azobenzene containing films upon irradiation with the intensity or polarization interference patterns. Two materials are studied differing in the molecular weight: an azobenzene-containing polymer and a molecular glass formed from a much smaller molecule consisting of three connected azobenzene units. Topography changes occurring along with the changes in irradiation conditions are recorded using a homemade set-up combining an optical part for generation and shaping of interference patterns and an atomic force microscope for acquiring the kinetics of film deformation. In this way, we could reveal the unique behavior of photosensitive materials during the first few minutes of irradiation: the change in topography is initially driven by an increase in the azobenzene free volume along with the trans-cis isomerization, followed by the mass transport finally resulting in the surface relief grating. This study demonstrates the great potential of our setup to experimentally highlight puzzling processes governing the formation of surface relief gratings.

  14. Determination of the Response Time of Photoanisotropy in Azobenzene Side-Chain Polyesters

    DEFF Research Database (Denmark)

    Bublitz, D.; Fleck, B.; Wenke, L.;

    2000-01-01

    sophisticated time resolving measuring equipment. The time resolution is in the order 10 ps and is comparable with the laser pulse duration. The response time of the azobenzene side-chain polyester E1aP has determined to be about 40 ps. (C) 2000 Elsevier Science B.V. All rights reserved....

  15. Biphotonic holographic gratings in azobenzene polyesters: Surface relief phenomena and polarization effects

    DEFF Research Database (Denmark)

    Sánchez, C.; Alcalá, R.; Hvilsted, Søren;

    2000-01-01

    Biphotonic holographic gratings have been recorded in a side-chain azobenzene liquid crystalline polyester using a blue incoherent source and a He-Ne laser. Intensity gratings and the appearance of surface relief have been observed when two linearly polarized beams from a He-Ne laser are made to...

  16. Theoretical model of photoinduced anisotropy in liquid-crystalline azobenzene side-chain polyesters

    DEFF Research Database (Denmark)

    Pedersen, Thomas Garm; Johansen, Per Michael; Holme, N.C.R.;

    1998-01-01

    A theoretical framework for the temporal behavior of photoinduced anisotropy in liquid-crystalline azobenzene side-chain polyesters is constructed. The domain structure of the material is taken into account and inter molecular interactions are included through a mean-field description. Photoinduced...

  17. Synthesis of azobenzene-containing liquid crystalline gelator for use in liquid crystal gels

    Institute of Scientific and Technical Information of China (English)

    Guang Wang; Xiao Liang Zhao; Yue Zhao

    2008-01-01

    A liquid crystalline gelator containing the azobenzene chromophore was synthesized for the first time; it was used to form self-assembled network in nematic liquid crystals resulting in liquid crystal gels with distinct features.? 2008 Guang Wang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

  18. Diffraction from polarization holographic gratings with surface relief in side-chain azobenzene polyesters

    DEFF Research Database (Denmark)

    Naydenova, I; Nikolova, L; Todorov, T;

    1998-01-01

    We investigate the polarization properties of holographic gratings in side-chain azobenzene polyesters in which an anisotropic grating that is due to photoinduced linear and circular birefringence is recorded in the volume of the material and a relief grating appears on the surface. A theoretical...

  19. Self-assembled monolayers of azobenzene functionalized 1,3,5-triazine-4,6-dithiols

    International Nuclear Information System (INIS)

    Two novel azobenzene-functionalized 1,3,5-triazine-4,6-dithiols were synthesized and their ultrathin films were prepared by self-assembling (SA) technique. The switching between trans-and cis-forms was observed by measuring the surface potential using the Kelvin probe technique while alternating irradiation the SA monolayer (SAM) with ultraviolet or visible light

  20. High diffraction efficiency polarization gratings recorded by biphotonic holography in an azobenzene liquid crystalline polyester

    DEFF Research Database (Denmark)

    Sánchez, C; Alcalá, R; Hvilsted, Søren;

    2001-01-01

    High diffraction efficiencies have been achieved with polarization gratings recorded in thin films of an azobenzene side-chain liquid crystalline polyester by means of biphotonic processes. Efficiency values up to 30% have been reached after an induction period of 300 s and subsequent evolution...

  1. Photoinduced anisotropy measurements in liquid-crystalline azobenzene side-chain polyesters

    DEFF Research Database (Denmark)

    Holme, NCR; Ramanujam, P.S.; Hvilsted, Søren

    1996-01-01

    Reversible photoinduced anisotropy in a series of Liquid-crystalline azobenzene side-chain polyesters is investigated as a function of intensity of the write beam and the sample temperature. Measurements reveal that the erasing takes place at a temperature much higher than the glass transition...... temperature. induced anisotropy can be erased by heating the polyesters to approximately 80 degrees C....

  2. Synthesis of Novel Amphiphilic Azobenzenes and X-ray Scattering Studies of Their Langmuir Monolayers

    DEFF Research Database (Denmark)

    Sørensen, Thomas Just; Kjær, Kristian; Breiby, Dag Werner;

    2008-01-01

    air-water interface, the amphiphilic azobenzenes form noncrystalline but stable Langmuir films that display an unusual reversible monolayer collapse close to 35 mN/m. The structures and phase transitions were studied by X-ray reflectivity (XR) and grazing-incidence X-ray diffraction, both utilizing...

  3. Holographic Gratings and Data Storage in Azobenzene-Containing Block Copolymers and Molecular Glasses

    Science.gov (United States)

    Audorff, Hubert; Kreger, Klaus; Walker, Roland; Haarer, Dietrich; Kador, Lothar; Schmidt, Hans-Werner

    This review covers synthesis, materials development, and photophysics of azobenzene-containing block copolymers as potential media for reversible volume holographic data storage. For high-density holographic data storage, volume gratings must be inscribed in millimeter-thick samples to achieve efficient angle multiplexing. It is demonstrated that block copolymers with azobenzene side-groups in the minority block develop no detrimental surface relief structures and exhibit superior performance regarding volume gratings, compared to homopolymers and statistical copolymers. Several material concepts for optimizing the refractive index modulation and the stability of volume gratings are presented. Stabilities of more than 2 years were achieved. Most important is the development of polymer blends comprising the azobenzene-containing block copolymer and an optically transparent homopolymer. This enables the preparation of millimeter-thick samples with the required optical density of ˜ 0. 7 at the writing wavelength by conventional injection molding techniques. The inscription of up to 200 holograms at the same lateral position was demonstrated. In addition, more than 1,000 write/erase cycles can be performed. This is the first time that the inscription and erasure of the long-term stable angle-multiplexed volume gratings in a rewritable polymeric medium have been achieved by purely optical means. A second important application for azobenzene-containing materials is the controlled preparation of surface relief structures. It is demonstrated that azobenzene-containing molecular glasses are an ideal class for efficient formation of surface relief gratings (SRGs) with amplitude heights of more than 600 nm. Clear relationships can be established between the chemical structure of the molecules and the behavior of SRG formation. All results are in agreement with the gradient force model by Kumar et al. The surface patterns are stable enough to be transferred to a polymer

  4. Azobenzene mesogen-passivated gold nanoparticles: Controlled preparation, self-organized superstructures, thermal behavior and photoisomerization

    International Nuclear Information System (INIS)

    Liquid crystal nanoscience has aroused intensive interests mainly due to their unique and collective properties and a variety of potential applications. In this paper, gold nanoparticles (GNPs) coated with alkoxy azobenzene mesogenic thiol ligands of different length polymethylene spacer and linear alkyl thiol co-ligands have been prepared. The thermal properties, phase behavior of thus obtained hybrid GNPs and photophysical properties of their solid-state films have been investigated by differential scanning calorimetry (DSC), variable-temperature small and wide angle X-ray scattering (SAXS/WAXS) and UV–vis spectroscopy. The hybrid GNPs exclusively passivated with azobenzene mesogenic ligands showed lamellar structure while those with mixed ligands exhibited hexagonal columnar superstructure, and the latter complex hybrid GNPs exhibited noticeably improved thermolysis resistance. Moreover, it is very interesting that the solid-state films of the hybrid GNPs displayed reversible photoresponse owing to the trans–cis transformation of azobenzene mesogenic ligands, and compared with the hybrid GNPs coated with mesogenic ligands only, those with mixed ligands exhibited faster photoisomerization rate upon alternate UV and visible light irradiation, which may have some promising applications. - Graphical abstract: Gold nanoparticles (GNPs) coated with azobenzene mesogenic thiol ligands and linear alkyl thiol co-ligands have been prepared showing lamellar or hexagonal columnar superstructures. The complex hybrid GNPs with co-ligands exhibit much improved thermolysis resistance and the solid-state films of the hybrid GNPs display interesting reversible photoisomerization. - Highlights: • Gold nanoparticles (GNPs) coated with azobenzene thiol ligands have been prepared. • The hybrid GNPs with alkyl thiol co-ligands show enhanced thermolysis resistance. • The hybrid GNPs exhibit lamellar or hexagonal columnar superstructures. • The solid-state films of the hybrid

  5. Studies on the permeability of polyacrylate and phosphate cements by means of 131I

    International Nuclear Information System (INIS)

    The permeability of a zinc phosphate cement and of a typical representative of the polyacrylate cements was studied radiometrically and autoradiographically, using 131I. The permeability of the phosphate cement was considerably greater than that of the polyacrylate cement. However, further studies evidenced that the penetrability of the polyacrylate cement increased markedly, which might be due to the contraction of the material. Compared with the findings of previous studies the permeability of a phosphate cement frequently used revealed to be equal to that of EBA cements and polyacrylate cements during the first day of setting. Thus, the EBA cements and the polyacrylate cements are not superior to zinc phosphate cements in this respect. (author)

  6. Microencapsulation of human fibroblasts in a water-insoluble polyacrylate.

    Science.gov (United States)

    Boag, A H; Sefton, M V

    1987-12-01

    Viable human diploid fibroblasts have been micro-encapsulated in EUDRAGIT RL, a commercially available water-insoluble polyacrylate, by an interfacial precipitation technique. Cells in medium and polymer solution (in diethyl phthalate) were coextruded and formed into droplets by a coaxial air stream. The droplets fell into a corn-oil/mineral-oil mixture to extract the solvent to precipitate the polymer around the cells. Capsules were ca. 500 mum in diameter depending on the air flowrate with a ca. 10-mum thick wall. When collagen (1 mg/mL) was added to the cell suspension prior to encapsulation and base-washed corn oil was used, cell growth occurred with one doubling achieved after five to six days as the collagen gel contracted inside the capsule. In the absence of collagen, cells spread on the inner wall of the capsule but did not grow, presumably because the surface charge on the capsule was inadequate. In similar fashion fibroblasts spread but did not grow on films of EUDRAGIT RL but did grow on blends of EUDRAGIT RL and EUDRAGIT E containing 10-30% of the latter more highly aminated polyacrylate. Although not suitable for anchorage-dependent cell growth by itself, EUDRAGIT RL has been suitable as a model polymer to demonstrate the feasibility of using water insoluble polyacrylates and organic solvents and nonsolvents for the micro-encapsulation of fibroblasts. Such microcapsules are of potential interest as a mode of large scale tissue culture for the production of novel therapeutic agents. PMID:18581534

  7. Characterization of linear and branched polyacrylates by tandem mass spectrometry.

    Science.gov (United States)

    Chaicharoen, Kittisak; Polce, Michael J; Singh, Anirudha; Pugh, Coleen; Wesdemiotis, Chrys

    2008-10-01

    The unimolecular degradation of alkali-metal cationized polyacrylates with the repeat unit CH(2)CH(COOR) and a variety of ester pendants has been examined by tandem mass spectrometry. The fragmentation patterns resulting from collisionally activated dissociation depend sensitively on the size of the ester alkyl substituent (R). With small alkyl groups, as in poly(methyl acrylate), lithiated or sodiated oligomers (M) decompose via free-radical chemistry, initiated by random homolytic C-C bond cleavages along the polymer chain. The radical ions formed this way dissociate further by backbiting rearrangements and beta scissions to yield a distribution of terminal fragments with one of the original end groups and internal fragments with 2-3 repeat units. If the ester alkyl group bears three or more carbon atoms, cleavages within the ester moieties become the predominant decomposition channel. This distinct reactivity is observed if R = t-butyl, n-butyl, or the mesogenic group (CH(2))(11)-O-C(6)H(4)-C(6)H(4)-CN. The [M+alkali metal](+) ions of the latter polyacrylates dissociate largely by charge-remote 1,5-H rearrangements that convert COOR to COOH groups by expulsion of 1-alkenes. The acid groups may displace an alcohol unit from a neighboring ester pendant to form a cyclic anhydride, unless hindered by steric effects. Using atom transfer radical polymerization, hyperbranched polyacrylates were prepared carrying ester groups both within and between the branches. Unique alkenes and alcohols are cleaved from ester groups at the branching points, enabling determination of the branching architecture. PMID:18373231

  8. QSPR Study on the Glass Transition Temperature of Polyacrylates

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Structural parameters of 22 polyacrylic compounds were computed at two levels using Hartree-Fock and DFT methods. Based on the experimental data of glass transition temperature (Tg), four-parameter (energy of the lowest unoccupied molecular orbital (ELOMO), the highest positive charge (Qmax+), dipole moments (μ) and the next highest occupied molecular orbital (ENLOMO)) dependent equations were developed using structural parameters as theoretical descriptors. Especially, Tg dependent equation calculated at the HF/6-31G(d) level is more advantageous than others in view of their correlation and predictive abilities. This dependent equation was validated by variance inflation factors (VIF) and t-test methods.

  9. Complex formation of calcium with humic acid and polyacrylic acid

    International Nuclear Information System (INIS)

    In order to understand the migration behavior of radionuclides in the underground, it is also important to estimate the effect of the competing cations originally present in the groundwater. In this connection, the complexation of Ca(II) with Aldrich humic acid has been examined. For the study at trace concentrations (∝ 10-10 M) of Ca(II), the solvent extraction of 45Ca with TTA and TOPO in cyclohexane has been used. At macro concentrations (10-4 M) of Ca(II), the measurement of the free Ca2+ ion concentration with a calcium selective electrode has been conducted. To estimate the polyelectrolyte effect of humic acid separately from its heterogeneous composition effect, polyacrylic acid ([-CH2CH(COOH)-]n) has been selected as a representative of the homogeneous polymeric weak acids and its complexation with Ca(II) has also been examined. The values of log βα have been obtained at pH 5 ∝ 7 in 0.1, 0.4 and 1.0 M NaCl, where βα is the apparent formation constants defined by βα = [ML]/([M][R]). In this definition, [ML] and [M] are the concentrations of bound and free Ca2+ respectively, [R] is the concentration of dissociated proton exchanging sites. log βα of humate decreases from 2.19 ∝ 2.92 (depending on pH and ionic strength 1.0 α of polyacrylate (1.36 ∝ 3.24 for I = 0.1 ∝ 1.0). For both humate and polyacrylate, log βα decreases linearly with log[Na+], where [Na+] is the bulk concentration of sodium ion. Their dependences of log βα on ionic strength are stronger than those of log β of monomeric carboxylates such as oxalate and EDTA, indicating the large electrostatic effect of crowded negative charges on the macromolecules of humic or polyacrylic acid. (orig.)

  10. Synthesis of polyacrylic-acid-based thermochromic polymers

    Science.gov (United States)

    Srivastava, Jyoti; Alam, Sarfaraz; Mathur, G. N.

    2003-10-01

    Smart materials respond to environmental stimuli with particular changes in some variables (for example temperature, pressure and electric field etc), for that reason they are often called responsive materials. In the present work, we have synthesized thermochromic polymer based on poly acrylic acid cobalt chloride (CoCl2) and phosphoric acid (H3PO4) that visually and reversibly changes color in the temperature range (70 - 130°C). These thermochromic materials can be used as visual sensors of temperature. Thermochromic polymers are based on polyacrylic acid and CoCl2 complex.

  11. The Humidity Sensor Using the Polyacrylic Emulsion Containing Magnesium Chloride

    Institute of Scientific and Technical Information of China (English)

    Ching-Han Yu; Jung-Chuan Chou; Tai-Ping Sun; Shen-Kan Hsiung

    2006-01-01

    An impedance type humidity sensor based on the polyacrylic emulsion containing magnesium chloride (MgCl2)without chemical modification was investigated. The impedances of the sensor were measured from various relative humidity in the frequency range between 0.1kHz and 100 kHz. The sensor has a good sensitivity from 60%RH to 90%RH. According to the experimental results, the response time is about 240 seconds in the adsorption process and 310 seconds in the desorption process.

  12. Radiation synthesis and characterization of polyacrylic acid hydrogels

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The pH-sensitive polyacrylic acid (PAA) hydrogels were synthesized by gamma-ray irradiation at an ambient temperature. The influences of dose, monomer concentration, cross-linking agent content, pH, and ionic strength on the swelling ratio (SR) of the PAA hydrogels were investigated in detail. The results show that the SR of the hydrogel decreases with an increase in the dose, monomer concentration, and cross-linking agent content. In alkaline solution, the SR of the hydrogels is much higher than that in acid solution. Also, the ionic strength can influence the SR of the hydrogels. The more the concentration, the lower the SR.

  13. Nickel adsorption by sodium polyacrylate-grafted activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Ewecharoen, A. [Division of Biotechnology, School of Bioresources and Technology, King Mongkut' s University of Technology Thonburi, 83 Moo 8 Thakham, Bangkhuntien, Bangkok 10150 (Thailand); Thiravetyan, P., E-mail: paitip@hotmail.com [Division of Biotechnology, School of Bioresources and Technology, King Mongkut' s University of Technology Thonburi, 83 Moo 8 Thakham, Bangkhuntien, Bangkok 10150 (Thailand); Wendel, E.; Bertagnolli, H. [Institut fuer Physikalische Chemie, Universitaet Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart (Germany)

    2009-11-15

    A novel sodium polyacrylate grafted activated carbon was produced by using gamma radiation to increase the number of functional groups on the surface. After irradiation the capacity for nickel adsorption was studied and found to have increased from 44.1 to 55.7 mg g{sup -1}. X-ray absorption spectroscopy showed that the adsorbed nickel on activated carbon and irradiation-grafted activated carbon was coordinated with 6 oxygen atoms at 2.04-2.06 A. It is proposed that this grafting technique could be applied to other adsorbents to increase the efficiency of metal adsorption.

  14. Nickel adsorption by sodium polyacrylate-grafted activated carbon.

    Science.gov (United States)

    Ewecharoen, A; Thiravetyan, P; Wendel, E; Bertagnolli, H

    2009-11-15

    A novel sodium polyacrylate grafted activated carbon was produced by using gamma radiation to increase the number of functional groups on the surface. After irradiation the capacity for nickel adsorption was studied and found to have increased from 44.1 to 55.7 mg g(-1). X-ray absorption spectroscopy showed that the adsorbed nickel on activated carbon and irradiation-grafted activated carbon was coordinated with 6 oxygen atoms at 2.04-2.06 A. It is proposed that this grafting technique could be applied to other adsorbents to increase the efficiency of metal adsorption. PMID:19576692

  15. Degradation of Sodium-Polyacrylate in Dilute Aqueous Solution

    Science.gov (United States)

    Saita, Takao

    1980-12-01

    It is shown using a capillary viscometer that the viscosity of a dilute aqueous solution of sodium-polyacrylate at 20°C decreases gradually for each flow time measurement and also decreases with the time of rest. Assuming that the polymer degradation is caused by shearing stress and oxidation, their effects are discussed with the data obtained using a closed-type capillary viscometer derived for this investigation. It is proved from the results that rupture of the Na-PAA molecule is caused by mechanochemical degradation, and also photo-degradation under the usual illumination and sunlight in a laboratory.

  16. Induction of mesenchymal stem cell chondrogenesis by polyacrylate substrates.

    Science.gov (United States)

    Glennon-Alty, Laurence; Williams, Rachel; Dixon, Simon; Murray, Patricia

    2013-04-01

    Mesenchymal stem cells (MSCs) can generate chondrocytes in vitro, but typically need to be cultured as aggregates in the presence of transforming growth factor beta (TGF-β), which makes scale-up difficult. Here we investigated if polyacrylate substrates modelled on the functional group composition and distribution of the Arg-Gly-Asp (RGD) integrin-binding site could induce MSCs to undergo chondrogenesis in the absence of exogenous TGF-β. Within a few days of culture on the biomimetic polyacrylates, both mouse and human MSCs, and a mesenchymal-like mouse-kidney-derived stem cell line, began to form multi-layered aggregates and started to express the chondrocyte-specific markers, Sox9, collagen II and aggrecan. Moreover, collagen II tended to be expressed in the centre of the aggregates, similarly to developing limb buds in vivo. Surface analysis of the substrates indicated that those with the highest surface amine content were most effective at promoting MSC chondrogenesis. These results highlight the importance of surface group functionality and the distribution of those groups in the design of substrates to induce MSC chondrogenesis. PMID:23237986

  17. Photoinduced reversible switching of porosity in molecular crystals based on star-shaped azobenzene tetramers

    Science.gov (United States)

    Baroncini, Massimo; D'Agostino, Simone; Bergamini, Giacomo; Ceroni, Paola; Comotti, Angiolina; Sozzani, Piero; Bassanetti, Irene; Grepioni, Fabrizia; Hernandez, Taylor M.; Silvi, Serena; Venturi, Margherita; Credi, Alberto

    2015-08-01

    The development of solid materials that can be reversibly interconverted by light between forms with different physico-chemical properties is of great interest for separation, catalysis, optoelectronics, holography, mechanical actuation and solar energy conversion. Here, we describe a series of shape-persistent azobenzene tetramers that form porous molecular crystals in their E-configuration, the porosity of which can be tuned by changing the peripheral substituents on the molecule. Efficient E→Z photoisomerization of the azobenzene units takes place in the solid state and converts the crystals into a non-porous amorphous melt phase. Crystallinity and porosity are restored upon Z→E isomerization promoted by visible light irradiation or heating. We demonstrate that the photoisomerization enables reversible on/off switching of optical properties such as birefringence as well as the capture of CO2 from the gas phase. The linear design, structural versatility and synthetic accessibility make this new family of materials potentially interesting for technological applications.

  18. Novel azobenzene-phthalocyanine dyads——design of photo-modulated J-aggregation

    Institute of Scientific and Technical Information of China (English)

    NIU LiHong; ZHONG Cheng; CHEN ZiHui; ZHANG Zhi; LI ZhongYu; ZHANG FuShi; TANG YingWu

    2009-01-01

    Based on the J-aggregation mechanism of α-aryl/alkoxy-subetituted zinc phthalocyanines(Pcs) in non-coordinating solvents, two novel azobenzene-phthalocyanine dyads (3-azo-ZnPc and 4-azo-ZnPc) were synthesized with the aim of developing Pc compounds whose ability to form J-aggregation could be photo-modulated. It was found that 3-azo-ZnPc in chloroform could be effectively photo-controlled in a wide range. This phenomenon could be explained by the changes in the geometry and dipole moment of azobenzene during the photo-isomerization process. 4-azo-ZnPc did not have this ability at all, with or without UV light illumination. The positions of the oxygen atoms to which the aryl/alkoxy substitution was attached relatively were found important in determining the aggregation ability.

  19. Photoresponsive switches at surfaces based on supramolecular functionalization with azobenzene-oligoglycerol conjugates.

    Science.gov (United States)

    Nachtigall, Olaf; Kördel, Christian; Urner, Leonhard H; Haag, Rainer

    2014-09-01

    The synthesis, supramolecular complexation, and switching of new bifunctional azobenzene-oligoglycerol conjugates in different environments is reported. Through the formation of host-guest complexes with surface immobilized β-cyclodextrin receptors, the bifunctional switches were coupled to gold surfaces. The isomerization of the amphiphilic azobenzene derivatives was examined in solution, on gold nanoparticles, and on planar gold surfaces. The wettability of functionalized gold surfaces can be reversibly switched under light-illumination with two different wavelengths. Besides the photoisomerization processes and concomitant effects on functionality, the thermal cis to trans isomerization of the conjugates and their complexes was monitored. Thermal half-lives of the cis isomers were calculated for different environments. Surprisingly, the half-lives on gold nanoparticles were significantly smaller compared to planar gold surfaces. PMID:25044973

  20. Elucidation of Isomerization Pathways of a Single Azobenzene Derivative Using an STM.

    Science.gov (United States)

    Kazuma, Emiko; Han, Mina; Jung, Jaehoon; Oh, Junepyo; Seki, Takahiro; Kim, Yousoo

    2015-11-01

    The predominant pathway for the isomerization between cis- and trans-azobenzenes-either (i) inversion by the bending of an NNC bond or (ii) rotation by the torsion of two phenyl rings-continues to be a controversial topic. To elucidate each isomerization pathway, a strategically designed and synthesized azobenzene derivative was investigated on a Ag(111) surface. This was achieved by exciting the molecule with tunneling electrons from the tip of a scanning tunneling microscope (STM). Structural analyses of the molecularly resolved STM images reveal that both inversion and rotation pathways are available for isomerization on a metal surface and strongly depend on the initial adsorption structures of the molecule. On the basis of the potential energy diagrams for the isomerization, it is concluded that isomerization pathways on a metal surface are not simply related to the excited states. PMID:26722964

  1. Mechanized azobenzene-functionalized zirconium metal-organic framework for on-command cargo release

    Science.gov (United States)

    Meng, Xiangshi; Gui, Bo; Yuan, Daqiang; Zeller, Matthias; Wang, Cheng

    2016-01-01

    Stimuli-responsive metal-organic frameworks (MOFs) have gained increasing attention recently for their potential applications in many areas. We report the design and synthesis of a water-stable zirconium MOF (Zr-MOF) that bears photoresponsive azobenzene groups. This particular MOF can be used as a reservoir for storage of cargo in water, and the cargo-loaded MOF can be further capped to construct a mechanized MOF through the binding of β-cyclodextrin with the azobenzene stalks on the MOF surface. The resulting mechanized MOF has shown on-command cargo release triggered by ultraviolet irradiation or addition of competitive agents without premature release. This study represents a simple approach to the construction of stimuli-responsive mechanized MOFs, and considering mechanized UiO-68-azo made from biocompatible components, this smart system may provide a unique MOF platform for on-command drug delivery in the future. PMID:27493996

  2. Photoresponsive Release from Azobenzene-Modified Single Cubic Crystal NaCl/Silica Particles

    Directory of Open Access Journals (Sweden)

    Xingmao Jiang

    2011-01-01

    Full Text Available Azobenzene ligands were uniformly anchored to the pore surfaces of nanoporous silica particles with single crystal NaCl using 4-(3-triethoxysilylpropylureidoazobenzene (TSUA. The functionalization delayed the release of NaCl significantly. The modified particles demonstrated a photocontrolled release by trans/cis isomerization of azobenzene moieties. The addition of amphiphilic solvents, propylene glycol (PG, propylene glycol propyl ether (PGPE, and dipropylene glycol propyl ether (DPGPE delayed the release in water, although the wetting behavior was improved and the delay is the most for the block molecules with the longest carbon chain. The speedup by UV irradiation suggests a strong dependence of diffusion on the switchable pore size. TGA, XRD, FTIR, and NMR techniques were used to characterize the structures.

  3. Orientation of azobenzene molecules in polymer films induced by all-optical poling

    Institute of Scientific and Technical Information of China (English)

    Xiaoxia Zhong(钟晓霞); Shouyu Luo(罗售余); Xiuqin Yu(虞秀琴); Qu Li(李劬); Yingli Chen(陈英礼); Yu Sui(隋郁); Jie Yin(印杰)

    2003-01-01

    A model of the alignment of azobenzene molecules in polymer film induced by all-optical poling is proposedand verified by experiment. We found that when the writing beams of frequencies ω and 2ω are both linearlypolarized with their polarization directions parallel to each other, azobenzene molecules tend to reorientto the direction perpendicular to the writing beams polarization. At the end of the writing process, moremolecules orient to the direction perpendicular to the writing beams polarization than those which orientto the parallel direction. The alignment of molecules parallel or perpendicular to the polarization of thewriting beams is characteristic of polarity or no polarity, respectively. The alignment of molecules alongthe polarization of writing beams results in the second order nonlinearity in the polymer film. Accordingto the model, a new method to improve the optical poling efficiency is put forward.

  4. Recent advances towards azobenzene-based light-driven real-time information-transmitting materials

    OpenAIRE

    Jaume García-Amorós; Dolores Velasco

    2012-01-01

    Photochromic switches that are able to transmit information in a quick fashion have attracted a growing interest within materials science during the last few decades. Although very fast photochromic switching materials working within hundreds of nanoseconds based on other chromophores, such as spiropyranes, have been successfully achieved, reaching such fast relaxation times for azobenzene-based photochromic molecular switches is still a challenge. This review focuses on the most recent achie...

  5. Kinetics of the photochromic reaction in a polymer containing azobenzene groups

    Czech Academy of Sciences Publication Activity Database

    Mancheva, I.; Zhivkov, I.; Nešpůrek, Stanislav

    2005-01-01

    Roč. 7, č. 1 (2005), s. 253-256. ISSN 1454-4164 R&D Projects: GA MŠk 1P04OCD14.30 Grant ostatní: Bulgarian Ministry of Education and Science(BG) x-1322 Keywords : photochromism * azobenzene * relaxation properties Subject RIV: BG - Nuclear, Atomic and Molecular Physics, Colliders Impact factor: 1.138, year: 2005

  6. Self-assembly of azobenzene bilayer membranes in binary ionic liquid-water nanostructured media.

    Science.gov (United States)

    Kang, Tejwant Singh; Ishiba, Keita; Morikawa, Masa-aki; Kimizuka, Nobuo

    2014-03-11

    Anionic azobenzene-containing amphiphile 1 (sodium 4-[4-(N-methyl-N-dodecylamino)phenylazo]benzenesulfonate) forms ordered bilayer membranes in binary ionic liquid (1-ethyl-3-methylimidazolium ethyl sulfate, [C2mim][C2OSO3])-water mixtures. The binary [C2mim][C2OSO3]-water mixture is macroscopically homogeneous at any mixing ratio; however, it possesses fluctuating nanodomains of [C2mim][C2OSO3] molecules as observed by dynamic light scattering (DLS). These nanodomains show reversible heat-induced mixing behavior with water. Although the amphiphile 1 is substantially insoluble in pure water, it is dispersible in the [C2mim][C2OSO3]-water mixtures. The concentration of [C2mim][C2OSO3] and temperature exert significant influences on the self-assembling characteristics of 1 in the binary media, as shown by DLS, transmission electron microscopy (TEM), UV-vis spectroscopy, and zeta-potential measurements. Bilayer membranes with rod- or dotlike nanostructures were formed at a lower content of [C2mim][C2OSO3] (2-30 v/v %), in which azobenzene chromophores adopt parallel molecular orientation regardless of temperature. In contrast, when the content of [C2mim][C2OSO3] is increased above 60 v/v %, azobenzene bilayers showed thermally reversible gel-to-liquid crystalline phase transition. The self-assembly of azobenzene amphiphiles is tunable depending on the volume fraction of [C2mim][C2OSO3] and temperature, which are associated with the solvation by nanoclusters in the binary [C2mim][C2OSO3]-water media. These observations clearly indicate that mixtures of water-soluble ionic liquids and water provide unique and valiant environments for ordered molecular self-assembly. PMID:24528277

  7. Trans-cis photoisomerization of azobenzene by n→π* excitation:A semiclassical dynamics study

    Institute of Scientific and Technical Information of China (English)

    Shuai Yuan; Wei Feng Wu; Yusheng Dou; Jian She Zhao

    2008-01-01

    A realistic dynamics simulation study is reported for the trans-cis photoisomerization of azobenzene triggered by the n→π*excitation and the results show that the formation of cis isomer follows the rotational motion around the N=N bond.The simulation find that the CNN bond angle bending vibrations also play a significant role in the vibronic coupling between the HOMO and LUMO,which essentially leads a nonadiabatic transition of the molecule to the electronic ground state.

  8. Influence of the substituent on azobenzene side-chain polyester optical storage materials

    DEFF Research Database (Denmark)

    Pedersen, M; Hvilsted, Søren; Holme, NCR;

    1999-01-01

    , chloro, and bromo. C-13 NMR spectroscopic and molecular mass investigations substantiate good film forming characteristics. The optical storage performance of thin polyester films are investigated through polarization holography. The resulting diffraction efficiency is mapped and discussed as a function...... of irradiation power and exposure time. Polytetradecanedioates with cyano-, nitro-, methyl-, fluoro-, or trinuoromethyl-azobenzene reach more than 50% diffraction efficiency. Investigations of anisotropy induced at different temperatures reveal that the polyesters are only photosensitive in a narrow...

  9. Development of a Nonionic Azobenzene Amphiphile for Remote Photocontrol of a Model Biomembrane.

    Science.gov (United States)

    Benedini, Luciano A; Sequeira, M Alejandra; Fanani, Maria Laura; Maggio, Bruno; Dodero, Verónica I

    2016-05-01

    We report the synthesis and characterization of a simple nonionic azoamphiphile, C12OazoE3OH, which behaves as an optically controlled molecule alone and in a biomembrane environment. First, Langmuir monolayer and Brewster angle microscopy (BAM) experiments showed that pure C12OazoE3OH enriched in the (E) isomer was able to form solidlike mesophase even at low surface pressure associated with supramolecular organization of the azobenzene derivative at the interface. On the other hand, pure C12OazoE3OH enriched in the (Z) isomer formed a less solidlike monolayer due to the bent geometry around the azobenzene moiety. Second, C12OazoE3OH is well-mixed in a biological membrane model, Lipoid s75 (up to 20%mol), and photoisomerization among the lipids proceeded smoothly depending on light conditions. It is proposed that the cross-sectional area of the hydroxyl triethylenglycol head of C12OazoE3OH inhibits azobenzenes H-aggregation in the model membrane; thus, the tails conformation change due to photoisomerization is transferred efficiently to the lipid membrane. We showed that the lipid membrane effectively senses the azobenzene geometrical change photomodulating some properties, like compressibility modulus, transition temperature, and morphology. In addition, photomodulation proceeds with a color change from yellow to orange, providing the possibility to externally monitor the system. Finally, Gibbs monolayers showed that C12OazoE3OH is able to penetrate the highly packing biomembrane model; thus, C12OazoE3OH might be used as photoswitchable molecular probe in real systems. PMID:27070294

  10. Characterization of azobenzene polymer networks using in situ solid state NMR and temperature dependent photostriction

    International Nuclear Information System (INIS)

    Azobenzene liquid crystal polymer networks (azo-LCNs) undergo a complex light-driven molecular conformation change of the azobenzene chromophore which imparts a macroscopic shape change within a glassy polymer network. To better understand molecular conformational changes which underlie macroscopic polymer deformation, we have collected solid-state nuclear magnetic resonance (NMR) data on 19F fluorinated side-chain azo-LCNs using an in situ visible light (450–458 nm) LED light source. We illustrate measurable changes in 19F NMR lineshapes under light irradiation, indicating that conformational changes can be probed by NMR. The measured effects of light on NMR spectra are also found to be reversible upon removal of the light source. We further show that sample heating does not affect azobenzene isomerization through analysis of temperature-dependent magic-angle-spinning NMR lineshapes. These results illustrate a narrowing of the lineshapes, but no change in the NMR peak positions, indicating that heating from 30 and 60 ° C affects molecular dynamics but does not change the azobenzene conformation. In addition to NMR data, benchtop photomechanical uni-axial measurements are taken over a temperature range from 23 to 60 ° C. Samples with the fluorinated side-chain azo-LCNs are compared to samples composed only of non-fluorinated main-chain azo-LCN composition. Similar stress relaxation was observed in both compositions under high pre-stretch. The amount of stress relaxation was found to depend on the pre-stretch, the ambient temperature, and the polarization of light. (paper)

  11. Electrochemical characterizations on MnO2 supercapacitors with potassium polyacrylate and potassium polyacrylate-co-polyacrylamide gel polymer electrolytes

    KAUST Repository

    Lee, Kuang-Tsin

    2009-11-01

    MnO2·nH2O supercapacitors with potassium polyacrylate (PAAK) and potassium polyacrylate-co-polyacrylamide (PAAK-co-PAAM) gel polymer electrolytes (GPEs) having the weight compositions of polymer:KCl:H2O = 9%:6.7%:84.3% have been characterized for their electrochemical performance. Compared with the liquid electrolyte (LE) counterpart, the GPE cells exhibit remarkable (∼50-130%) enhancement in specific capacitance of the oxide electrode, and the extent of the enhancement increases with increasing amount of the carboxylate groups in the polymers as well as with increasing oxide/electrolyte interfacial area. In situ X-ray absorption near-edge structure (XANES) analysis indicates that the oxide electrodes of the GPE cells possess higher Mn-ion valences and are subjected to greater extent of valence variation than that of the LE cell upon charging/discharging over the same potential range. Copolymerization of PAAK with PAAM greatly improves the cycling stability of the MnO2·nH2O electrode, and the improvement is attributable to the alkaline nature of the amino groups. Both GPEs exhibit ionic conductivities greater than 1.0 × 10-1 S cm-1 and are promising for high-rate applications. © 2009 Elsevier Ltd. All rights reserved.

  12. Light-enhanced liquid-phase exfoliation and current photoswitching in graphene-azobenzene composites

    Science.gov (United States)

    Döbbelin, Markus; Ciesielski, Artur; Haar, Sébastien; Osella, Silvio; Bruna, Matteo; Minoia, Andrea; Grisanti, Luca; Mosciatti, Thomas; Richard, Fanny; Prasetyanto, Eko Adi; de Cola, Luisa; Palermo, Vincenzo; Mazzaro, Raffaello; Morandi, Vittorio; Lazzaroni, Roberto; Ferrari, Andrea C.; Beljonne, David; Samorì, Paolo

    2016-04-01

    Multifunctional materials can be engineered by combining multiple chemical components, each conferring a well-defined function to the ensemble. Graphene is at the centre of an ever-growing research effort due to its combination of unique properties. Here we show that the large conformational change associated with the trans-cis photochemical isomerization of alkyl-substituted azobenzenes can be used to improve the efficiency of liquid-phase exfoliation of graphite, with the photochromic molecules acting as dispersion-stabilizing agents. We also demonstrate reversible photo-modulated current in two-terminal devices based on graphene-azobenzene composites. We assign this tuneable electrical characteristics to the intercalation of the azobenzene between adjacent graphene layers and the resulting increase in the interlayer distance on (photo)switching from the linear trans-form to the bulky cis-form of the photochromes. These findings pave the way to the development of new optically controlled memories for light-assisted programming and high-sensitive photosensors.

  13. Surface hopping dynamics of direct trans --> cis photoswitching of an azobenzene derivative in constrained adsorbate geometries

    Science.gov (United States)

    Floß, Gereon; Granucci, Giovanni; Saalfrank, Peter

    2012-12-01

    With ongoing miniaturization of electronic devices, the need for individually addressable, switchable molecules arises. An example are azobenzenes on surfaces which have been shown to be switchable between trans and cis forms. Here, we examine the "direct" (rather than substrate-mediated) channel of the trans → cis photoisomerization after ππ* excitation of tetra-tert-butyl-azobenzene physisorbed on surfaces mimicking Au(111) and Bi(111), respectively. In spirit of the direct channel, the electronic structure of the surface is neglected, the latter merely acting as a rigid platform which weakly interacts with the molecule via Van-der-Waals forces. Starting from thermal ensembles which represent the trans-form, sudden excitations promote the molecules to ππ*-excited states which are non-adiabatically coupled among themselves and to a nπ*-excited and the ground state, respectively. After excitation, relaxation to the ground state by internal conversion takes place, possibly accompanied by isomerization. The process is described here by "on the fly" semiclassical surface hopping dynamics in conjunction with a semiempirical Hamiltonian (AM1) and configuration-interaction type methods. It is found that steric constraints imposed by the substrate lead to reduced but non-vanishing, trans → cis reaction yields and longer internal conversion times than for the isolated molecule. Implications for recent experiments for azobenzenes on surfaces are discussed.

  14. Nonadiabatic simulation study of photoisomerization of azobenzene: Detailed mechanism and load-resisting capacity

    CERN Document Server

    Shao, Junfeng; Wen, Zhenyi; Dou, Yusheng; Wang, Zhisong

    2009-01-01

    Nonadiabatic dynamical simulations were carried out to study cis-to-trans isomerization of azobenzene under laser irradiation and/or external mechanical loads. We used a semiclassical electron-radiation-ion dynamics method that is able to describe the coevolution of the structural dynamics and the underlying electronic dynamics in a real-time manner. It is found that azobenzene photoisomerization occurs predominantly by an out-of-plane rotation mechanism even under a nontrivial resisting force of several tens of piconewtons. We have repeated the simulations systematically for a broad range of parameters for laser pulses, but could not find any photoisomerization event by a previously suggested in-plane inversion mechanism. The simulations found that the photoisomerization process can be held back by an external resisting force of 90 - 200 pN depending on the frequency and intensity of the lasers. This study also found that a pure mechanical isomerization is possible from the cis state if the azobenzene molecu...

  15. Optical Input/Electrical Output Memory Elements based on a Liquid Crystalline Azobenzene Polymer.

    Science.gov (United States)

    Mosciatti, Thomas; Bonacchi, Sara; Gobbi, Marco; Ferlauto, Laura; Liscio, Fabiola; Giorgini, Loris; Orgiu, Emanuele; Samorì, Paolo

    2016-03-01

    Responsive polymer materials can change their properties when subjected to external stimuli. In this work, thin films of thermotropic poly(metha)acrylate/azobenzene polymers are explored as active layer in light-programmable, electrically readable memories. The memory effect is based on the reversible modifications of the film morphology induced by the photoisomerization of azobenzene mesogenic groups. When the film is in the liquid crystalline phase, the trans → cis isomerization induces a major surface reorganization on the mesoscopic scale that is characterized by a reduction in the effective thickness of the film. The film conductivity is measured in vertical two-terminal devices in which the polymer is sandwiched between a Au contact and a liquid compliant E-GaIn drop. We demonstrate that the trans → cis isomerization is accompanied by a reversible 100-fold change in the film conductance. In this way, the device can be set in a high- or low-resistance state by light irradiation at different wavelengths. This result paves the way toward the potential use of poly(metha)acrylate/azobenzene polymer films as active layer for optical input/electrical output memory elements. PMID:26890532

  16. Light-enhanced liquid-phase exfoliation and current photoswitching in graphene–azobenzene composites

    Science.gov (United States)

    Döbbelin, Markus; Ciesielski, Artur; Haar, Sébastien; Osella, Silvio; Bruna, Matteo; Minoia, Andrea; Grisanti, Luca; Mosciatti, Thomas; Richard, Fanny; Prasetyanto, Eko Adi; De Cola, Luisa; Palermo, Vincenzo; Mazzaro, Raffaello; Morandi, Vittorio; Lazzaroni, Roberto; Ferrari, Andrea C.; Beljonne, David; Samorì, Paolo

    2016-01-01

    Multifunctional materials can be engineered by combining multiple chemical components, each conferring a well-defined function to the ensemble. Graphene is at the centre of an ever-growing research effort due to its combination of unique properties. Here we show that the large conformational change associated with the trans–cis photochemical isomerization of alkyl-substituted azobenzenes can be used to improve the efficiency of liquid-phase exfoliation of graphite, with the photochromic molecules acting as dispersion-stabilizing agents. We also demonstrate reversible photo-modulated current in two-terminal devices based on graphene–azobenzene composites. We assign this tuneable electrical characteristics to the intercalation of the azobenzene between adjacent graphene layers and the resulting increase in the interlayer distance on (photo)switching from the linear trans-form to the bulky cis-form of the photochromes. These findings pave the way to the development of new optically controlled memories for light-assisted programming and high-sensitive photosensors. PMID:27052205

  17. Photo-induced and thermal reactions in thin films of an azobenzene derivative on Bi(111)

    International Nuclear Information System (INIS)

    Azobenzene is a prototypical molecular switch which can be interconverted with UV and visible light between a trans and a cis isomer in solution. While the ability to control their conformation with light is lost for many molecular photoswitches in the adsorbed state, there are some examples for successful photoisomerization in direct contact with a surface. However, there the process is often driven by a different mechanism than in solution. For instance, photoisomerization of a cyano-substituted azobenzene directly adsorbed on Bi(111) occurs via electronic excitations in the substrate and subsequent charge transfer. In the present study we observe two substrate-mediated trans–cis photoisomerization reactions of the same azobenzene derivative in two different environments within a multilayer thin film on Bi(111). Both processes are associated with photoisomerization and one is around two orders of magnitude more efficient than the other. Furthermore, the cis isomers perform a thermally induced reaction which may be ascribed to a back-isomerization in the electronic ground state or to a phenyl ring rotation of the cis isomer

  18. Tuning the optical emission of MoS2 nanosheets using proximal photoswitchable azobenzene molecules

    International Nuclear Information System (INIS)

    We report photoluminescence measurements performed on monolayer- and two-layer-MoS2 placed on two types of mixed self-assembled monolayers (mSAMs) of photoswitchable azobenzene molecules. The two mSAMs differ via the electronegative character of the azobenzene derivatives. Thin layers of a transition metal dichalcogenide—MoS2—were mechanically exfoliated on mSAM to allow for direct interaction between the molecules and the MoS2 layers. When the MoS2 nanosheet is in contact with the electropositive azobenzene molecules in trans configuration, an emission side band at lower energies and at low excitation powers suggest n-type doping. The photoisomerization of the molecules from trans to cis configuration lowers the doping, quenching the side band and enhancing the overall PL efficiency by a factor of ∼3. Opposite results were observed with the chlorinated, more electronegative molecules, exhibiting a reversed trend in the PL efficiency between trans and cis, but with an overall larger intensity. The type of doping induced by the two types of mSAMs was determined by Kelvin probe force microscopy technique

  19. Photomechanical bending mechanics of polydomain azobenzene liquid crystal polymer network films

    International Nuclear Information System (INIS)

    Glassy, polydomain azobenzene liquid crystal polymer networks (azo-LCNs) have been synthesized, characterized, and modeled to understand composition dependence on large amplitude, bidirectional bending, and twisting deformation upon irradiation with linearly polarized blue-green (440-514 nm) light. These materials exhibit interesting properties for adaptive structure applications in which the shape of the photoresponsive material can be rapidly reconfigured with light. The basis for the photomechanical output observed in these materials is absorption of actinic light by azobenzene, which upon photoisomerization dictates an internal stress within the local polymer network. The photoinduced evolution of the underlying liquid crystal microstructure is manifested as macroscopic deformation of the glassy polymer film. Accordingly, this work examines the polarization-controlled bidirectional bending of highly concentrated azo-LCN materials and correlates the macroscopic output (observed as bending) to measured blocked stresses upon irradiation with blue-green light of varying polarization. The resulting photomechanical output is highly dependent on the concentration of crosslinked azobenzene mesogens employed in the formulation. Experiments that quantify photomechanical bending and photogenerated stress are compared to a large deformation photomechanical shell model to quantify the effect of polarized light interactions with the material during static and dynamic polarized light induced deformation. The model comparisons illustrate differences in internal photostrain and deformation rates as a function of composition and external mechanical constraints.

  20. The Modification of Sodium Polyacrylate Water Solution Cooling Properties by AL2O3

    OpenAIRE

    Wojciech Gęstwa; Małgorzata Przyłęcka

    2010-01-01

    This paper presents a preliminary examination of water cooling ability as a result of its modification by the addition of sodium polyacrylate and AL2O3 nanoparticles. (AL2O3) alumina oxide was present in gamma phase as a form of nanopowder whose particle size was less than 50 nm. Cooling curves in the temperature-time system were marked for the three cooling media: water, 10% water solution of sodium polyacrylate, and 10% water solution of sodium polyacrylate with 1% addition of AL2O3 nanopar...

  1. Synthesis of copper polyacrylate nanocomposites by gamma irradiation

    International Nuclear Information System (INIS)

    This research involves the synthesis of copper nanoparticles with controlled size by the application of gamma radiation with varying polyacrylic acid (PAA) and CuSO4 concentration. An alternative and convenient method was done which employs Co60 irradiation of solutions of copper salt and PAA with irradiation dose of 1.6, 3.6, 6.4, and 9.2 MRad. The effect of polymer and copper sulfate's initial concentrations as well as the effect of the presence of alcohol as radical scavenger and the presence of ethylenediaminetetraacetic acid as stabilizer were evaluated. Characterization of nanocomposite properties such as plasmon resonance band, fluorescence, and particle morphology and size were determined. Layer-by-layer assembly of Cu-PAA nanocomposites and polydiallyl dimethyl ammonium chloride (PDDA) was also constructed. Stability of the synthesized copper-PAA nanocomposites in terms of the disappearance of plasmon band with time was evaluated. (Author)

  2. Nanometer TiO2 Modified Polyacrylic Copolymer Sizing Agent

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A series of new-type nanometer TiO2 modified polyacrylic copolymer sizing agent were synthesized from acrylic acid, ethyl acrylate, nanometer TiO2, oleic acid etc.by orthogonal design method. Results of the studies show that the synthetic method used in this paper was a new way and had never been found in the synthesis of acrylate sizing agent, and that the properties of those new-type size-agent were be improved, which had potential for substituting PVA (polyvinyl alcohol) sizing agent. The technology for solving the problem of nano-scale powder agglomeration and dispersion were also studied. The transmission electron microscope (TEM) observation showed that nano-TiO2 had good dispersion and stability in aqueous solution and in sizing agent solution.

  3. The cis-state of an azobenzene photoswitch is stabilized through specific interactions with a protein surface.

    Science.gov (United States)

    Korbus, Michael; Backé, Sarah; Meyer-Almes, Franz-Josef

    2015-03-01

    The photocontrol of protein function like enzyme activity has been the subject of many investigations to enable reversible and spatiotemporally defined cascading biochemical reactions without the need for separation in miniaturized and parallelized assay setups for academic and industrial applications. A photoswitchable amidohydrolase variant from Bordetella/Alcaligenes with the longest reported half-life (approximately 30 h) for the cis-state of the attached azobenzene group was chosen as a model system to dissect the underlying mechanism and molecular interactions that caused the enormous deceleration of the thermal cis-to-trans relaxation of the azobenzene photoswitch. A systematic site-directed mutagenesis study on the basis of molecular dynamics simulation data was employed to investigate enzyme and thermal cis-to-trans relaxation kinetics in dependence on selected amino acid substitution, which revealed a prominent histidine and a hydrophobic cluster as molecular determinants for the stabilization of the cis-isomer of the attached azobenzene moiety on the protein surface. The nature of the involved interactions consists of polar, hydrophobic, and possibly aromatic Π-Π contributions. The elucidated principles behind the stabilization of the cis-state of azobenzene derivatives on a protein surface can be exploited to design improved biologically inspired photoswitches. Moreover, the findings open the door to highly long-lived cis-states of azobenzene groups yielding improved bistable photoswitches that can be controlled by single light-pulses rather than continuous irradiation with UV light that causes potential photodamage to the employed biomolecules. PMID:25664524

  4. Complex formation of Eu(III) with polyacrylic acid

    International Nuclear Information System (INIS)

    For the quantitative description of the interaction of metal ions with humic substances, it is necessary to clarify the effects of both polyelectrolyte and heterogeneous nature of humic substances. To estimate the polyelectrolyte effect separately, polyacrylic acid (MW = 90 000) has been selected as a representative of well-defined, homogeneous polymeric weak acids, and its interaction with Eu(III) has been investigated by a solvent extraction method using 152Eu (∝ 10-8 M) with TTA and TBP in xylene. By defining the apparent complex formation constant as βα = [ML]/([M][R]), where [M] = [Eu3+], [ML] is the concentration of Eu(III) associated with polyacrylic acid and [R] = CRα (CR is a total concentration of proton exchanging sites and α is a degree of dissociation determined by potentiometric titration), the apparent constants have been obtained at several pcH and ionic strength (0.1 M and 1.0 M NaClO4). The constants increased with pcH and decreased with an increase of ionic strength, that is, the values of log βα varied from 6.0 (at pcH = 4.7) to 7.6 (pcH = 5.5) at 0.1 M NaClO4 and from 4.8 (pcH = 4.4) to 6.5 (pcH = 5.4) at 1.0 M. The plots of log βα versus log α revealed almost linear relationship both at 0.1 and 1.0 M NaClO4. (orig.)

  5. Mechanical behaviour characterizing and simulation of polyacrylate rubber

    Directory of Open Access Journals (Sweden)

    D. dos Santos

    2010-01-01

    Full Text Available Purpose: of this paper is to investigate the influence of EB radiation on the mechanical behaviour of UV curing polyacrylate rubber (ACM and to simulate its behaviour.Design/methodology/approach: The material was irradiated by two different EB doses, 100 kGy and 250 kGy, its mechanical behaviour was investigated with the help of uniaxial, equibiaxial and planar shear experiments. The results were applied to the Ogden’s Model (1972 in order to obtain the parameters to simulate the material behaviour by finite element method (FEM and to compare experimental and FEM curves. The structure molecular changes caused by EB were investigated with the help of infrared spectroscopy.Findings: In most cases the experimental results showed an increase in the strength at rupture and a decrease in the elongation at the rupture with increasing of radiation dose. Equibiaxial and planar shear tests presented similar behaviour like uniaxial results, in terms of elongation decrease and strength increase, with some deviations. Ogden’s Model third order provided simulated curves with similar behaviour in comparison to experimental curves. The infrared spectroscopy showed different chemical group contents in the analyzed regions, surface and middle region.Research limitations/implications: Two doses of EB radiation were applied; higher or lower doses were not investigated.Practical implications: Improved behaviour of UV curing ACM can extend the range of industrial applications, or improve its performance in known applications.Originality/value: Usually EB radiation has been used to modify polymeric structure and to improve thermal and mechanical polymers behaviour. Regarding like rubber materials EB is usually applied as an alternative form of vulcanization. UV is a new type of curing for polyacrylate rubbers, which are usually cured by thermal processes.

  6. STUDIES ON THE BLEND OF POLYACRYLATE EMULSIONS AND TACKIFIER RESIN EMULSIONS

    Institute of Scientific and Technical Information of China (English)

    HU Shuwen; YANG Yukun

    1996-01-01

    A series of polyacrylate emulsions were blended with tackifier resin emulsions such as modified rosin emulsion, C5 resin and C9 resin emulsion. The miscibility of the polyacrylates and tackifier resins was investigated by means of SEM and visual observation. The phase diagrams of the miscibility change systematically with the polarity of polyacrylates and tackifier resins. The influence of the content of the tackifier resins on the adhesion properties of the polyacrylate emulsions were also studied. The results show that the 180℃ peel strength is improved as the amount of the tackifier resin increases and comes to a maximum at a specific content. The ball tack property decreases slightly and the hold strength changes complicatedly as the tackifier resin increases.

  7. Investigation of Polyacrylate Anion-Exchangers for Separation of Rare Earth Element Complexes with EDTA

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The rare earth complexes with EDTA, Ln(edta), show an unusual sequence of affinity for the anion-exchangers. The sorption and chromatographic separation of Y3+ for Nd3+ complexes with EDTA was studied by using the strongly basic gel and macroporous polyacrylate anion-exchangers, Amberlite IRA 458 and Amberlite 958, and the weakly basic gel polyacrylate anion-exchanger, Amberlite IRA-68. The investigations on sorption and separation of rare earth complexes with EDTA on the polyacrylate anion-exchangers applied mainly in the environment protection so far indicate that they can be applied in anionexchange separation of lanthanide complexes with aminopolycarboxylic acids. It was shown that the weakly basic polyacrylate gel anion-exchanger Amberlite IRA-68 is the most effective in purification of Y3+ from Nd3+ in comparison with the strongly basic anion-exchangers of this type.

  8. Research on the chemical mechanism in the polyacrylate latex modified cement system

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Min [The Key Laboratory of Space Applied Physics and Chemistry, Ministry of Education and Shaanxi Key Laboratory of Macromolecular Science and Technology, School of Science, Northwestern Polytechnical University, Xi' an 710072 (China); Wang, Rumin, E-mail: wangmin19@mail.nwpu.edu.cn [The Key Laboratory of Space Applied Physics and Chemistry, Ministry of Education and Shaanxi Key Laboratory of Macromolecular Science and Technology, School of Science, Northwestern Polytechnical University, Xi' an 710072 (China); Zheng, Shuirong [The Key Laboratory of Space Applied Physics and Chemistry, Ministry of Education and Shaanxi Key Laboratory of Macromolecular Science and Technology, School of Science, Northwestern Polytechnical University, Xi' an 710072 (China); Northwestern Polytechnical University–East China University of Science and Technology Combined Research Institute of New High Speed Railway Materials (China); Farhan, Shameel; Yao, Hao; Jiang, Hao [The Key Laboratory of Space Applied Physics and Chemistry, Ministry of Education and Shaanxi Key Laboratory of Macromolecular Science and Technology, School of Science, Northwestern Polytechnical University, Xi' an 710072 (China)

    2015-10-15

    In this paper, the chemical mechanism in the polyacrylate latex modified cement system was investigated by Fourier transform infrared spectra (FT-IR), X-ray photoelectron spectroscopy (XPS), gel permeation chromatography (GPC) and compact pH meter. All results have shown that the chemical reactions in the polyacrylate modified system can be divided into three stages. The hydration reactions of cement can produce large amounts of Ca(OH){sub 2} (calcium hydroxide) and lead the whole system to be alkali-rich and exothermic at the first stage. Subsequently, this environment can do great contributions to the hydrolysis of ester groups in the polyacrylate chains, resulting in the formation of carboxyl groups at the second stage. At the third stage, the final crosslinked network structure of the product was obtained by the reaction between the carboxyl groups in the polyacrylate latex chains and Ca(OH){sub 2}.

  9. Research on the chemical mechanism in the polyacrylate latex modified cement system

    International Nuclear Information System (INIS)

    In this paper, the chemical mechanism in the polyacrylate latex modified cement system was investigated by Fourier transform infrared spectra (FT-IR), X-ray photoelectron spectroscopy (XPS), gel permeation chromatography (GPC) and compact pH meter. All results have shown that the chemical reactions in the polyacrylate modified system can be divided into three stages. The hydration reactions of cement can produce large amounts of Ca(OH)2 (calcium hydroxide) and lead the whole system to be alkali-rich and exothermic at the first stage. Subsequently, this environment can do great contributions to the hydrolysis of ester groups in the polyacrylate chains, resulting in the formation of carboxyl groups at the second stage. At the third stage, the final crosslinked network structure of the product was obtained by the reaction between the carboxyl groups in the polyacrylate latex chains and Ca(OH)2

  10. Cross-linked polyacrylates in post-mining substrates: persistence and effects on plant growth

    OpenAIRE

    Rodionov, A.; S. Nii-Annang; Fischer, T.; Gattinger, A.; Bens, O.; Raab, T.; R. F. Hüttl

    2014-01-01

    Application of hydrophilic polymers composed of cross-linked polyacrylate can improve soil water-holding capacity and accelerate the restoration of post-mining substrates. In this work, we studied the persistence of a polyacrylate polymer incorporated into a soil and its impact on plant nutrients at a reclamation site of former lignite mining in Lusatia (Germany). In contrast to autumn application, the incorporation of the polymer enhanced the sequestration of plant-derived carbon in the soil...

  11. Molecular modeling studies of interactions between sodium polyacrylate polymer and calcite surface

    International Nuclear Information System (INIS)

    The interactions between calcite pigment and sodium polyacrylate dispersing agent, widely used in papermaking as paper coating components, were investigated using classical force field and quantum chemical approaches. The objective was to understand interactions between the calcite surface and sodium polyacrylate polymer at 300 K using molecular dynamics simulations. A quantum mechanical ab initio Hartree–Fock method was also used to obtain detailed information about the sodium polyacrylate polymer structure. The effect of water molecules (moisture) on the interactions was also examined. Calculations showed that molecular weight, branching and the orientation of sodium polyacrylate polymers influence the interactions between the calcite surface and the polymer. The force field applied, and also water molecules, were found to have an impact on all systems studied. Ab initio Hartree–Fock calculations indicated that there are two types of coordination between sodium atoms and carboxylate groups of the sodium polyacrylate polymer, inter- and intra-carboxylate group coordination. In addition, ab initio Hartree–Fock calculations of the structure of the sodium polyacrylate polymer produced important information regarding interactions between the polymers and carboxylated styrene-butadiene latex particles.

  12. Molecular modeling studies of interactions between sodium polyacrylate polymer and calcite surface

    Energy Technology Data Exchange (ETDEWEB)

    Ylikantola, A. [University of Jyväskylä, Department of Chemistry, P.O. Box 35, University of Jyväskylä, FI-40014 (Finland); Linnanto, J., E-mail: juha.m.linnanto@gmail.com [University of Jyväskylä, Department of Chemistry, P.O. Box 35, University of Jyväskylä, FI-40014 (Finland); University of Tartu, Institute of Physics, Riia 142, EE-51014 Tartu (Estonia); Knuutinen, J.; Oravilahti, A. [University of Jyväskylä, Department of Chemistry, P.O. Box 35, University of Jyväskylä, FI-40014 (Finland); Toivakka, M. [Åbo Akademi University, Laboratory of Paper Coating and Converting and Center for Functional Materials, FI-20500 Turku/Åbo (Finland)

    2013-07-01

    The interactions between calcite pigment and sodium polyacrylate dispersing agent, widely used in papermaking as paper coating components, were investigated using classical force field and quantum chemical approaches. The objective was to understand interactions between the calcite surface and sodium polyacrylate polymer at 300 K using molecular dynamics simulations. A quantum mechanical ab initio Hartree–Fock method was also used to obtain detailed information about the sodium polyacrylate polymer structure. The effect of water molecules (moisture) on the interactions was also examined. Calculations showed that molecular weight, branching and the orientation of sodium polyacrylate polymers influence the interactions between the calcite surface and the polymer. The force field applied, and also water molecules, were found to have an impact on all systems studied. Ab initio Hartree–Fock calculations indicated that there are two types of coordination between sodium atoms and carboxylate groups of the sodium polyacrylate polymer, inter- and intra-carboxylate group coordination. In addition, ab initio Hartree–Fock calculations of the structure of the sodium polyacrylate polymer produced important information regarding interactions between the polymers and carboxylated styrene-butadiene latex particles.

  13. Molecular modeling studies of interactions between sodium polyacrylate polymer and calcite surface

    Science.gov (United States)

    Ylikantola, A.; Linnanto, J.; Knuutinen, J.; Oravilahti, A.; Toivakka, M.

    2013-07-01

    The interactions between calcite pigment and sodium polyacrylate dispersing agent, widely used in papermaking as paper coating components, were investigated using classical force field and quantum chemical approaches. The objective was to understand interactions between the calcite surface and sodium polyacrylate polymer at 300 K using molecular dynamics simulations. A quantum mechanical ab initio Hartree-Fock method was also used to obtain detailed information about the sodium polyacrylate polymer structure. The effect of water molecules (moisture) on the interactions was also examined. Calculations showed that molecular weight, branching and the orientation of sodium polyacrylate polymers influence the interactions between the calcite surface and the polymer. The force field applied, and also water molecules, were found to have an impact on all systems studied. Ab initio Hartree-Fock calculations indicated that there are two types of coordination between sodium atoms and carboxylate groups of the sodium polyacrylate polymer, inter- and intra-carboxylate group coordination. In addition, ab initio Hartree-Fock calculations of the structure of the sodium polyacrylate polymer produced important information regarding interactions between the polymers and carboxylated styrene-butadiene latex particles.

  14. Photo-induced morphological winding and unwinding motion of nanoscrolls composed of niobate nanosheets with a polyfluoroalkyl azobenzene derivative

    Science.gov (United States)

    Nabetani, Yu; Takamura, Hazuki; Uchikoshi, Akino; Hassan, Syed Zahid; Shimada, Tetsuya; Takagi, Shinsuke; Tachibana, Hiroshi; Masui, Dai; Tong, Zhiwei; Inoue, Haruo

    2016-06-01

    Photo-responsive nanoscrolls can be successfully fabricated by mixing a polyfluoroalkyl azobenzene derivative and a niobate nanosheet, which is exfoliated from potassium hexaniobate. In this study, we have found that the photo-responsive nanoscroll shows a morphological motion of winding and unwinding, which is basically due to the nanosheet sliding within the nanoscroll, by efficient photo-isomerization reactions of the intercalated azobenzene in addition to the interlayer distance change of the nanoscrolls. The relative nanosheet sliding of the nanoscroll is estimated to be ca. 280 nm from the AFM morphology analysis. The distance of the sliding motion is over 20 times that of the averaged nanosheet sliding in the azobenzene/niobate hybrid film reported previously. Photo-responsive nanoscrolls can be expected to be novel photo-activated actuators and artificial muscle model materials.Photo-responsive nanoscrolls can be successfully fabricated by mixing a polyfluoroalkyl azobenzene derivative and a niobate nanosheet, which is exfoliated from potassium hexaniobate. In this study, we have found that the photo-responsive nanoscroll shows a morphological motion of winding and unwinding, which is basically due to the nanosheet sliding within the nanoscroll, by efficient photo-isomerization reactions of the intercalated azobenzene in addition to the interlayer distance change of the nanoscrolls. The relative nanosheet sliding of the nanoscroll is estimated to be ca. 280 nm from the AFM morphology analysis. The distance of the sliding motion is over 20 times that of the averaged nanosheet sliding in the azobenzene/niobate hybrid film reported previously. Photo-responsive nanoscrolls can be expected to be novel photo-activated actuators and artificial muscle model materials. Electronic supplementary information (ESI) available: Fig. S1. Photo-isomerization reaction of nanoscrolls. See DOI: 10.1039/c6nr02177h

  15. Fabrication of narrow surface relief features in a side-chain azobenzene polyester with a scanning near-field microscope

    DEFF Research Database (Denmark)

    Ramanujam, P.S.; Holme, N. C. R.; Pedersen, M.;

    2001-01-01

    We show that it is possible to fabricate topographic submicron features in a side-chain azobenzene polyester with a scanning near-field optical microscope, Through irradiation at a wavelength of 488 run at intensity levels of 12 W/cm(2), topographic features as narrow as 240 nm and as high as 6 nm...... have been reproducibly recorded in a thin film of the polyester. These observations are consistent with the fact that at low intensities peaks are produced evolving into formation of trenches at high intensities in the case of amorphous side-chain azobenzene polyesters. This may find applications in...

  16. Vibrational spectra study of phosphorus dendrimer containing azobenzene, ammonium and carbamate groups

    Science.gov (United States)

    Furer, V. L.; Vandyukov, A. E.; Majoral, J. P.; Caminade, A. M.; Kovalenko, V. I.

    2013-06-01

    The FTIR and FT Raman spectra of the first generation dendrimers, possessing carbamate (G1) or ammonium (G2) terminal groups were studied. The structural optimization and normal mode analysis were performed for dendrimers on the basis of the density functional theory (DFT). These calculations of G2 gave the frequencies of vibrations, infrared intensities and Raman scattering activities for the E- and Z-forms of azobenzene unit. The energy difference between the E- and Z-forms of G2 is 27.36 kcal/mol. The calculated geometrical parameters and harmonic vibrational frequencies are predicted in a good agreement with the experimental data. It was found that dendrimers molecules have a concave lens structure with planar -O-C6H4-CHdbnd N-N(CH3)Pdbnd S, and -O-C6H4-Ndbnd N-C6H4-CHdbnd N-NH-Cdbnd O-CH2-N fragments and slightly non-planar cyclotriphosphazene core. The experimental IR and Raman spectra of dendrimers G1 and G2 were interpreted by means of potential energy distributions. Relying on DFT calculations a complete vibrational assignment is proposed. The strong band 1605 cm-1 in the IR spectra show marked changes of the optical density in dependence of substituents in the aromatic ring. The differences in the IR and Raman spectra of G2 for the E- and Z-forms of azobenzene units were cleared up. During structural isomerization of azobenzene units, redistribution of band intensities appears to a much higher extent than frequency shifts.

  17. Study on the prediction of visible absorption maxima of azobenzene compounds

    OpenAIRE

    Liu, Jun-Na; Chen, Zhi-Rong; Yuan, Shen-feng

    2005-01-01

    The geometries of azobenzene compounds are optimized with B3LYP/6-311G* method, and analyzed with nature bond orbital, then their visible absorption maxima are calculated with TD-DFT method and ZINDO/S method respectively. The results agree well with the observed values. It was found that for the calculation of visible absorption using ZINDO/S method could rapidly yield better results by adjusting OWFπ-π (the relationship between π-π overlap weighting factor) value than by the TD-DFT method. ...

  18. Influence of the substituent on azobenzene side-chain polyester optical storage materials

    DEFF Research Database (Denmark)

    Pedersen, M; Hvilsted, Søren; Holme, NCR; Berg, RH

    1999-01-01

    A number of poly(1,3-propylenetetradecanedioates) or poly(1,3-propyleneadipates) with pendant p-substitued azobenzenes linked through a hexylene spacer in the 2-position are prepared. The substituents comprise: cyano, nitro, methoxy, hydrogen, methyl, n-butyl, phenyl, fluoro, trifluoromethyl......, chloro, and bromo. C-13 NMR spectroscopic and molecular mass investigations substantiate good film forming characteristics. The optical storage performance of thin polyester films are investigated through polarization holography. The resulting diffraction efficiency is mapped and discussed as a function...

  19. C5-Azobenzene-substituted 2'-Deoxyuridine-containing Oligodeoxynucleotides for Photo-Switching Hybridization

    Directory of Open Access Journals (Sweden)

    Shohei Mori

    2014-04-01

    Full Text Available A new photoisomeric nucleoside dUAz bearing an azobenzene group at the C5-position of 2'-deoxyuridine was designed and synthesized. Photoisomerization of dUAz in oligodeoxynucleotides can be achieved rapidly and selectively with 365 nm (forward and 450 nm (backward irradiation. Thermal denaturation experiments revealed that dUAz stabilized the duplex in the cis-form and destabilized it in the trans-form with mismatch discrimination ability comparable to thymidine. These results indicate that dUAz could be a powerful material for reversibly manipulating nucleic acid hybridization with spatiotemporal control.

  20. Photomechanical Response of Composite Structures Built from Azobenzene Liquid Crystal Polymer Networks

    Directory of Open Access Journals (Sweden)

    Kyung Min Lee

    2011-09-01

    Full Text Available Optically directed shape adaptive responses have been sought after for many decades in photoresponsive polymeric materials. A number of recent examinations have elucidated elucidated the unique opportunities of photomechanical responses realized in azobenzene-functionalized liquid crystalline polymer networks (both elastomers and glasses. This work summarizes and contrasts the photomechanical response of glassy polydomain, monodomain, and twisted nematic azo-LCN materials to blue-green irradiation. Building from this summary, the combinatorial photomechanical response observed upon irradiation of composite cantilevers is examined. Large scale shape adaptations are realized, with novel responses that may be of potential use in future employment of these materials in actuation.

  1. Azobenzene Modified Imidacloprid Derivatives as Photoswitchable Insecticides: Steering Molecular Activity in a Controllable Manner

    Science.gov (United States)

    Xu, Zhiping; Shi, Lina; Jiang, Danping; Cheng, Jiagao; Shao, Xusheng; Li, Zhong

    2015-10-01

    Incorporating the photoisomerizable azobenzene into imidacloprid produced a photoswitchable insecticidal molecule as the first neonicotinoid example of remote control insecticide performance with spatiotemporal resolution. The designed photoswitchable insecticides showed distinguishable activity against Musca both in vivo and in vitro upon irradiation. Molecular docking study further suggested the binding difference of the two photoisomers. The generation of these photomediated insecticides provides novel insight into the insecticidal activity facilitating further investigation on the functions of insect nicotinic acetylcholine receptors and opens a novel way to control and study insect behavior on insecticide poisoning using light.

  2. Photoresponsive Toroidal Nanostructure Formed by Self-Assembly of Azobenzene-Functionalized Tris(phenylisoxazolyl)benzene.

    Science.gov (United States)

    Adachi, Hiroaki; Hirai, Yuko; Ikeda, Toshiaki; Maeda, Makoto; Hori, Ryo; Kutsumizu, Shoichi; Haino, Takeharu

    2016-03-01

    The self-assembly of tris(phenylisoxazolyl)benzene 1b with photochemically addressable azobenzene moieties produced toroidal nanostructures, the formation and dissociation of which were reversibly regulated upon photoirradiation. 1b displayed a mesogenic behavior. In the solution, the stacked assemblies along with their C3 axes were formed. In the mesophase, two molecules of 1b most likely adopted the antiparallel arrangement to stabilize the columnar organization. This assembling behavior most likely triggered the development of the supramolecular toroidal nanostructures. PMID:26910789

  3. Continuously tunable laser based on polarization gratings in azobenzene-containing material

    International Nuclear Information System (INIS)

    Two simple procedures to manufacture continuously tunable miniature lasers in azobenzene-containing material were developed. Both types of lasers rely on the distributed feedback provided by polarization gratings. In a first approach tuning is achieved by changing the thickness of the active wave guiding layer by means of a wedge layer and in a second approach by gradually changing the spatial frequency of the refractive index grating obtained by modification of the Lloyd interferometer set-up used for holographic inscription of the gratings. A continuous tuning range of up to 35 nm has been demonstrated. (paper)

  4. Optical and Physical Applications of Photocontrollable Materials: Azobenzene-Containing and Liquid Crystalline Polymers

    Directory of Open Access Journals (Sweden)

    Takashi Fukuda

    2012-01-01

    Full Text Available Photocontrol of molecular alignment is an exceptionally-intelligent and useful strategy. It enables us to control optical coefficients, peripheral molecular alignments, surface relief structure, and actuation of substances by means of photoirradiation. Azobenzene-containing polymers and functionalized liquid crystalline polymers are well-known photocontrollable materials. In this paper, we introduce recent applications of these materials in the fields of mechanics, self-organized structuring, mass transport, optics, and photonics. The concepts in each application are explained based on the mechanisms of photocontrol. The interesting natures of the photocontrollable materials and the conceptual applications will stimulate novel ideas for future research and development in this field.

  5. Impact of sodium polyacrylate on the amorphous calcium carbonate formation from supersaturated solution.

    Science.gov (United States)

    Liu, J; Pancera, S; Boyko, V; Gummel, J; Nayuk, R; Huber, K

    2012-02-21

    A detailed in situ scattering study has been carried out on the formation of amorphous calcium carbonate (ACC) particles modulated by the presence of small amounts of sodium polyacrylate chains. The work is aiming at an insight into the modulation of ACC formation by means of two polyacrylate samples differing in their molecular weight by a factor of 50. The ACC formation process was initiated by an in situ generation of CO(3)(2-) ions via hydrolysis of 10 mM dimethylcarbonate in the presence of 10 mM CaCl(2). Analysis of the formation process by means of time-resolved small-angle X-ray and light scattering in the absence of any additives provided evidence for a monomer addition mechanism for the growth of ACC particles. ACC formation under these conditions sets in after a lag-period of some 350 s. In the presence of sodium polyacrylate chains, calcium polyacrylate aggregates are formed during the lag-period, succeeded by a modulated ACC growth in a second step. The presence of anionic polyacrylate chains changed the shape of the growing particles toward loose and less homogeneous entities. In the case of low amounts (1.5-7.5 mg/L) of the long chain additive with 97 kDa, the size of the aggregates is comparable to the size of the successively formed hybrid particles. No variation of the lag-period has been observed in this case. Use of the short chain additive with 2 kDa enabled increase of the additive concentration up to 100 mg/L and resulted in a significant increase of the lag-period. This fact, together with the finding that the resulting hybrid particles remained stable in the latter case, identified short chain sodium polyacrylates as more efficient modulators than long chain polyacrylates. PMID:22256962

  6. trans-cis photoisomerization of azobenzene-conjugated dithiolato-bipyridine platinum(II) complexes: extension of photoresponse to longer wavelengths and photocontrollable tristability.

    Science.gov (United States)

    Sakamoto, Ryota; Kume, Shoko; Sugimoto, Manabu; Nishihara, Hiroshi

    2009-01-01

    Azobenzene derivatives modified with dithiolato-bipyridine platinum(II) complexes were synthesized, revealing their highly extended photoresponses to the long wavelength region as well as unique photocontrollable tristability. The absorptions of trans-1 and trans-2 with one azobenzene group on the dithiolene and bipyridine ligands, respectively, cover the range from 300 to 700 nm. These absorptions are ascribed, by means of time-dependent (TD)DFT calculations, to transitions from dithiolene(pi) to bipyridine(pi*), namely, interligand charge transfer (CT), pi-pi*, and n-pi* transitions of the azobenzene unit, and pi-pi* transitions of the bipyridine ligand. In addition, only trans-1 shows distinctive electronic bands, assignable to transitions from the dithiolene(pi) to azobenzene(pi*), defined as intraligand CT. Complex 1 shows photoisomerization behavior opposite to that of azobenzene: trans-to-cis and cis-to-trans conversions proceed with 405 and 312 nm irradiation, which correspond to excitation with the intraligand CT, and pi-pi* bands of the azobenzene and bipyridine units, respectively. In contrast, complex 2 shows photoisomerization similar to that of azobenzene: trans-to-cis and cis-to-trans transformations occur with 365 and 405 nm irradiation, respectively. Irradiation at 578 nm, corresponding to excitation of the interligand CT transitions, results in cis-to-trans conversion of both 1 and 2, which is the longest wavelength ever reported to effect the photoisomerization of the azobenzene group. The absorption and photochromism of 4, which has azobenzene groups on both the dithiolato and bipyridine ligands, have characteristics quite similar to those of 1 and 2, which furnishes 4 with photocontrollable tristability in a single molecule using light at 365, 405, and 578 nm. We also clarified that 1 and 2 have high photoisomerization efficiencies, and good thermal stability of the cis forms. Complexes 3 and 5 have almost the identical photoresponse to those

  7. Omniphobic low moisture permeation transparent polyacrylate/silica nanocomposite.

    Science.gov (United States)

    Hsu, Sheng-Hao; Chang, Yuan-Ling; Tu, Yu-Chieh; Tsai, Chieh-Ming; Su, Wei-Fang

    2013-04-24

    We report the development of low moisture permeation and transparent dense polyacrylate/silica nanocomposite material that can exhibit both superhydrophobic and oleophobic (omniphobic) properties. The material was prepared by a three-step process. The first step involved the preparation of UV polymerizable solventless hybrid resin and the fabrication of nanocomposite. The hybrid resin consisted of a mixture of acrylate monomer, initiator, and acrylate-modified different size silica nanoparticles. The second step was to roughen the surface of the nanocomposite with unique nanotexture by oxygen plasma. In the third step, we applied a low surface tension fluoro monolayer on the treated surface. The nanocomposite exhibits desired superhydrophobicity and oleophobicity with a water contact angle of 158.2° and n-1-octadecene contact angle of 128.5°, respectively; low moisture permeation of 1.44 g·mm/m(2)·day; and good transparency (greater than 82% at 450-800 nm for ~60 μm film). The material has potential applications in optoelectronic encapsulation, self-cleaning coating, etc. PMID:23496768

  8. Antimicrobial activity of poly(acrylic acid) block copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Gratzl, Günther, E-mail: guenther.gratzl@jku.at [Johannes Kepler University Linz, Institute for Chemical Technology of Organic Materials, Altenberger Str. 69, 4040 Linz (Austria); Paulik, Christian [Johannes Kepler University Linz, Institute for Chemical Technology of Organic Materials, Altenberger Str. 69, 4040 Linz (Austria); Hild, Sabine [Johannes Kepler University Linz, Institute of Polymer Science, Altenberger Str. 69, 4040 Linz (Austria); Guggenbichler, Josef P.; Lackner, Maximilian [AMiSTec GmbH and Co. KG, Leitweg 13, 6345 Kössen, Tirol (Austria)

    2014-05-01

    The increasing number of antibiotic-resistant bacterial strains has developed into a major health problem. In particular, biofilms are the main reason for hospital-acquired infections and diseases. Once formed, biofilms are difficult to remove as they have specific defense mechanisms against antimicrobial agents. Antimicrobial surfaces must therefore kill or repel bacteria before they can settle to form a biofilm. In this study, we describe that poly(acrylic acid) (PAA) containing diblock copolymers can kill bacteria and prevent from biofilm formation. The PAA diblock copolymers with poly(styrene) and poly(methyl methacrylate) were synthesized via anionic polymerization of tert-butyl acrylate with styrene or methyl methacrylate and subsequent acid-catalyzed hydrolysis of the tert-butyl ester. The copolymers were characterized via nuclear magnetic resonance spectroscopy (NMR), size-exclusion chromatography (SEC), Fourier transform infrared spectroscopy (FTIR), elemental analysis, and acid–base titrations. Copolymer films with a variety of acrylic acid contents were produced by solvent casting, characterized by atomic force microscopy (AFM) and tested for their antimicrobial activity against Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. The antimicrobial activity of the acidic diblock copolymers increased with increasing acrylic acid content, independent of the copolymer-partner, the chain length and the nanostructure. - Highlights: • Acrylic acid diblock copolymers are antimicrobially active. • The antimicrobial activity depends on the acrylic acid content in the copolymer. • No salts, metals or other antimicrobial agents are needed.

  9. Vesicles prepared with the complex salts dioctadecyldimethylammonium polyacrylates.

    Science.gov (United States)

    Alves, Fernanda Rosa; Loh, Watson

    2012-02-15

    The effect of a polymeric counterion on the thermotropic behavior of sonicated vesicles formed by complex salts in aqueous solution and with decanol (C(10)OH) and tetradecanol (C(14)OH) was investigated. The complex salts were prepared with dioctadecyldimethylammonium bromide (DODAB) and polyacrylic acids (PAA, containing 30 or 6000 repeating units), being referred to as DODAPA(30) and DODAPA(6000). Vesicles containing polymeric counterions presented higher contents of multilamellar vesicles that were dependent on the complex salt concentration and on the counterion chain length. For comparison, studies were performed with DODAAc, with the counterion acetate, resulting in the formation of mostly unilamellar vesicles, as expected due greater dissociation, leading to greater electrical repulsion between bilayers. Mixtures of these complex salts and DODAX (where X=acetate or bromide) were also investigated with respect to their vesicles thermotropic behavior and size. This study opens the possibility of applying the methodology of direct complex salt preparation (as opposed to mixing the surfactant and polymeric components) to produce vesicles with controlled composition and properties. PMID:22172692

  10. XPS study of graphite - Polymer interfaces of polyacrylate composites

    International Nuclear Information System (INIS)

    Complete text of publication follows. Polyacrylate - acrylamide - graphite composite samples were prepared via frontal polymerization. Three different types of acrylate monomers were used to prepare samples and eight different samples were prepared with each type of acrylate monomers. The acrylate/acrylamide monomer ratio was varied between 0.1 and 7.5. The graphite concentration was constant in all samples. To verify or disprove polymer - graphite interactions in the composites, the composite - graphite interfaces were studied by Al K-alpha excited XPS, using a custom made high energy resolution electron spectrometer in fixed retardation mode. Primary spectra showed by 2-4 shouldered structures in the C 1s. O 1s peaks were also studied, however less structured peaks and shoulders were found than in the cases of C 1s. On the basis of literature, a typical bound energy was assign to the C and O atoms in different chemical bond states. On the basis of these facts, the C 1s and O 1s photopeaks were decomposed according to different chemical bond states. Thus an ambiguous connection has been found between the acrylate/acrylamide molar ratio and peak ratio. The chemical bound formed between the polymer and graphite in the composites has also been verified. (author)

  11. Antimicrobial activity of poly(acrylic acid) block copolymers

    International Nuclear Information System (INIS)

    The increasing number of antibiotic-resistant bacterial strains has developed into a major health problem. In particular, biofilms are the main reason for hospital-acquired infections and diseases. Once formed, biofilms are difficult to remove as they have specific defense mechanisms against antimicrobial agents. Antimicrobial surfaces must therefore kill or repel bacteria before they can settle to form a biofilm. In this study, we describe that poly(acrylic acid) (PAA) containing diblock copolymers can kill bacteria and prevent from biofilm formation. The PAA diblock copolymers with poly(styrene) and poly(methyl methacrylate) were synthesized via anionic polymerization of tert-butyl acrylate with styrene or methyl methacrylate and subsequent acid-catalyzed hydrolysis of the tert-butyl ester. The copolymers were characterized via nuclear magnetic resonance spectroscopy (NMR), size-exclusion chromatography (SEC), Fourier transform infrared spectroscopy (FTIR), elemental analysis, and acid–base titrations. Copolymer films with a variety of acrylic acid contents were produced by solvent casting, characterized by atomic force microscopy (AFM) and tested for their antimicrobial activity against Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. The antimicrobial activity of the acidic diblock copolymers increased with increasing acrylic acid content, independent of the copolymer-partner, the chain length and the nanostructure. - Highlights: • Acrylic acid diblock copolymers are antimicrobially active. • The antimicrobial activity depends on the acrylic acid content in the copolymer. • No salts, metals or other antimicrobial agents are needed

  12. Collapse of sodium polyacrylate chains in calcium salt solutions

    Science.gov (United States)

    Schweins, R.; Huber, K.

    The sodium salt of polyacrylic acid (NaPA) precipitates in the presence of Ca^{2+}-ions. This phase behaviour can be represented by a phase diagram where the critical NaPA concentration is plotted versus the critical Ca^{2+} concentration resulting in a straight line as a phase boundary. The location of this phase boundary is influenced by the presence of an inert monovalent salt like NaCl. The present contribution focuses on the coil dimensions of NaPA chains in dilute aqueous solution corresponding to the one phase region of such a phase diagram. A variety of parameters with which the size and shape of the polyelectrolyte chains can be modulated are revealed. Approaching the phase boundary by decreasing the NaPA concentration at a constant Ca^{2+} content leads to a collapse of the NaPA chains. Combined static and dynamic light scattering suggests a compact spherical shape as the final state of this transition, both in 0.1 M NaCl and in 0.01 M NaCl. In the lower NaCl concentration, indication is presented for the existence of a cigar or pearl necklace like intermediate. Most strikingly, the collapsed chains can be reexpanded by increasing the concentration of inert NaCl at constant content of NaPA and Ca^{2+}. Clearly, excessive Na+-ions displace the Ca^{2+}-ions from the NaPA chains.

  13. Properties of Polyacrylate Latex Prepared Under Different Emulsified Systems

    Institute of Scientific and Technical Information of China (English)

    CHEN Lijun; WU Fengqin

    2012-01-01

    The polyacrylate latexes were synthesized via pre-emulsified and semi-continuous seeded emulsion polymerization technology when conventional surfactant or polymerizable surfactant was used as emulsifiers.The resultant latexes and their films were characterized with the contact angle determinator and rheometer.Effect of the polymerizable surfactant on water resistance,stability and rheology of the latex was studied.Results show that the water resistance of film is increased first then decreased with the increase of the amount of the polymerizable surfactant.There exists the optimum value of the amount of the polymerizable surfactant for the water resistance of the film.In comparison with the latex prepared with the conventional surfactant,both the mechanical stability and the freezing-thaw stability of the latex are improved when the polymerizable surfactant is used during the course of the emulsion polymerization.The resultant latex has rheological properties of pseudo-plastic fluid and belongs to non-Newtonian fluid.

  14. Ab initio calculation of the electronic spectrum of azobenzene dyes and its impact on the design of optical data storage materials

    DEFF Research Database (Denmark)

    Åstrand, Per-Olof; Ramanujam, P.S.; Hvilsted, Søren; Bak, K.L.; Sauer, S.P.A.

    2000-01-01

    Electronic excitation energies of 16 azobenzene dyes have been calculated by ab initio methods within the second-order polarization propagator approximation (SOPPA). Good agreement with expriment is found for the lowest singlet and triplet states for both the trans- and cis-azobenzene molecules......V. Furthermore, the experimental singlet π → π* transitions are reproduced for a set of azobenzene dyes with different electron donor and acceptor groups and the correct shifts in excitation energy are obtained for the different substituents. It has also been demonstrated that ab initio methods can be used to...... determine suitable candidates for azo components used in materials for data storage....

  15. Gating the photochromism of an azobenzene by strong host-guest interactions in a divalent pseudo[2]rotaxane.

    Science.gov (United States)

    Lohse, Mirko; Nowosinski, Karol; Traulsen, Nora L; Achazi, Andreas J; von Krbek, Larissa K S; Paulus, Beate; Schalley, Christoph A; Hecht, Stefan

    2015-06-18

    The ability of an E-configured azobenzene guest to undergo photoisomerisation is controlled by the presence of a complementary host. Addition of base/acid allowed for a weakening/strengthening of the interactions in the divalent pseudo[2]rotaxane complex and hence could switch on/off photochromic activity. PMID:25929291

  16. Temperature- and Photocontrolled Unfolding/Folding of a Triple-Helical Azobenzene-Stapled Collagen Peptide Monitored by Infrared Spectroscopy.

    Science.gov (United States)

    Lorenz, Lisa; Kusebauch, Ulrike; Moroder, Luis; Wachtveitl, Josef

    2016-05-01

    The triple-helical structure of a model collagen peptide possessing azobenzene-derived clamps integrated in all three strands as side-chain-to-side-chain crosslinks is analyzed by IR spectroscopy in comparative thermal excursion experiments with the triple helix of a typical reference collagen peptide consisting of only glycine-proline-hydroxyproline repeats. By exploiting the known stabilizing effects of aqueous alcoholic solvents on the unique collagen fold, deuterated ethylene glycol/water (1:1) is used as a solvent to investigate the effect of the light-switchable trans/cis-azobenzene clamp on the stability of the triple helix in terms of H/D exchange rates and thermal unfolding. Results of this comparative analysis clearly reveal only a minor destabilization of the triple helix by the hydrophobic azobenzene moieties compared to the reference collagen peptide as reflected by a lower midpoint of the thermal unfolding and higher rates of H/D exchange. However, it also reveals that the driving force exerted by the trans-to-cis photoisomerization of the azobenzene moieties is insufficient for unfolding of the compact triple-helical collagen fold. Only temperature-dependent untightening of this fold with heating results in a reversible photomodulated unfolding and refolding of the azo-collagen peptide into the original triple helix. PMID:26918674

  17. Synthesis of poly glycidylmethacrylate grafted azobenzene copolymer: Photosensitivity and nonlinear optical properties

    Science.gov (United States)

    Sousani, Abbas; Moghadam, Peyman Najafi; Hasanzadeh, Reza; Motiei, Hamideh; Bagheri, Massoumeh

    2016-01-01

    In this work poly glycidylmethacrylate grafted 4-hydroxy-4‧-methoxy-azobenzene (Azo-PGMA) was synthesized. For this propose firstly 4-hydroxy-4‧-methoxy-azobenzene (AZO) was prepared, then poly glycidylmethacrylate was prepared by free radical polymerization of glycidylmethacrylate in the presence of benzoyl peroxide as initiator under inert atmosphere in dry THF. Finally the homopolymer was functionalized by AZO moieties. The characterization of the synthesized copolymer was carried out by 1H NMR, FT-IR, thermal gravimetric analyze (TGA), differential scanning calorimetry (DSC) and optical polarizing microscope (POM) analysis. The UV-vis studies were carried out on Azo-PGMA copolymer and the results showed that the synthesized Azo-PGMA copolymer has ultra-fast response to UV light and has slow relaxation time. Also the third-order nonlinear optical properties of the Azo-PGMA copolymer and AZO were studied by using Z-scan technique. Nonlinear refraction and absorption coefficients of the above mentioned materials were measured by the closed and open aperture Z-scan method using a continuous wave Nd-YAG laser at 532 nm. The positive nonlinear absorption in Azo-PGMA and AZO was investigated at the wavelength of λ = 532 nm, respectively and the measured values of nonlinear refraction in both of the samples were from the order of 10-8 cm2/W.

  18. Photomodulation of fluoride ion binding through anion-π interactions using a photoswitchable azobenzene system

    Science.gov (United States)

    Rananaware, Anushri; Samanta, Mousumi; Bhosale, Rajesh S.; Kobaisi, Mohammad Al; Roy, Biswajit; Bheemireddy, Varun; Bhosale, Sidhanath V.; Bandyopadhyay, Subhajit; Bhosale, Sheshanath V.

    2016-03-01

    The discovery of photoswitchable azobenzene-systems that undergo trans-to-cis photoisomerisation was a milestone in supramolecular chemistry. Such photoswitches have possible applications in data storage, stimuli responsive delivery systems, and molecular machines due to fast and selective switching. However, the light induced cis isomer of azobenzene is rather unstable and reverts thermally and photochemically to the thermodynamically stable trans configuration. We report, for the first time, controlled photoswitching of an azo-naphthalenediimide (azo-NDI) which can be achieved upon binding of fluoride ions through anion-π interaction. This NDI-F–NDI “sandwich” stabilises the cis configuration through the generation of an NDI•‑ radical anion, and a dianionic, NDI2‑ species that becomes unusually stable in the cis form. The sandwiched cis form reverts to the trans form only upon decomplexation of F‑. A model pollutant was successfully degraded using the photogenerated NDI-F–NDI sandwich. This opens a wide range of applications in molecular and supramolecular nanotechnology.

  19. Surface modification of magnetite nanoparticle with azobenzene-containing water dispersible polymer

    International Nuclear Information System (INIS)

    We here report the synthesis of magnetite nanoparticle (MNP) grafted with poly (ethylene glycol) methyl ether methacrylate (PEGMA)-azobenzene acrylate (ABA) statistical copolymer via atom transfer radical polymerization (ATRP) for drug entrapment and photocontrolled release. MNP was synthesized via thermal decomposition of iron (III) acetylacetonate in benzyl alcohol and surface functionalized to obtain ATRP initiating sites. Molar compositions of the copolymer on MNP surface were systematically varied (100:0, 90:10, 70:30, and 50:50 of PEGMA:ABA, respectively) to obtain water dispersible particles with various amounts of azobenzene. The presence of polymeric shell on MNP core was evidenced by transmission electron microscopy (TEM). Drug loading and entrapment efficiencies as well as drug release behavior of the copolymer–MNP complexes were investigated. It was found that when percent of ABA in the copolymers was increased, entrapment and loading efficiencies of prednisolone model drug were enhanced. Releasing rate and percent of the released prednisolone of the complex exposed in UV light were slightly enhanced as compared to the system without UV irradiation. This copolymer–MNP complex with photocontrollable drug release and magnetic field-directed properties is warranted for further studies for potential uses as a novel drug delivery vehicle.

  20. Nonadiabatic hybrid quantum and molecular mechanic simulations of azobenzene photoswitching in bulk liquid environment.

    Science.gov (United States)

    Böckmann, Marcus; Doltsinis, Nikos L; Marx, Dominik

    2010-01-21

    A nonadiabatic hybrid quantum and molecular mechanical (na-QM/MM) molecular dynamics scheme has been implemented recently combining the nonadiabatic Car-Parrinello molecular dynamics method by Doltsinis and Marx [Phys. Rev. Lett. 2002, 88, 166402] with the QM/MM coupling approach by Laio et al. [J. Chem. Phys. 2002, 116, 6941]. Here an extensive validation of the underlying, density functional theory based, electronic structure methods by comparison to CASPT2 ab initio data is presented for the case of azobenzene. The "on the fly" na-QM/MM method is then applied to study Z-->E and E-->Z photoisomerization of azobenzene in a bulk liquid environment. The isomerization mechanism is found to be a pedal motion of the central CN horizontal lineNC group in both cases. While the Z-->E reaction is barely affected by the environment, E-->Z photoisomerization is slowed down considerably in the liquid compared to the gas phase. This effect is due to the fact that reorientation of the phenyl rings is significantly hindered in the liquid by steric nearest neighbor interactions. Nonradiative decay is found to be substantially faster for Z-AB (subpicosecond regime) than for E-AB (picosecond regime). The main molecular motions responsible for nonadiabatic coupling have been identified as the oscillations in the NN and CN bond lengths, the CNN bond angles, and the CNNC dihedral angle. PMID:19928885

  1. The effect of TiO2/aluminosilicate nanocomposite additives on the mechanical and thermal properties of polyacrylic coatings

    Science.gov (United States)

    Nosrati, Rahimeh; Olad, Ali

    2015-12-01

    The commercial grade polyacrylic latex was modified in order to prepare a mechanical and thermal improved coating. TiO2/Ag-exchanged-aluminosilicate nanocomposites with montmorillonite, zeolite-A and clinoptilolite aluminosilicates were prepared and used as additive in the matrix of polyacrylic latex to achieve a coating with proper mechanical and thermal properties. X-ray diffraction patterns and FESEM were used to characterize the composition, structure, and morphology of the nanocomposite additives. Polyacrylic coatings modified by TiO2/Ag-exchanged-aluminosilicate nanocomposite additives showed higher adhesion strength and hardness compared to unmodified commercial grade polyacrylic coatings. Differential Scanning Calorimetry (DSC) analysis showed lower glass transition temperature for modified polyacrylic coatings than that of unmodified polyacrylic coatings. The tensile tests were also carried out for unmodified and modified polyacrylic coatings. According to the results, the modified polyacrylic based coating with TiO2/Ag-exchanged-clinoptilolite nanocomposite additive was the best coating considering most of useful properties.

  2. Nanosilica and Polyacrylate/Nanosilica: A Comparative Study of Acute Toxicity

    Directory of Open Access Journals (Sweden)

    Ying-Mei Niu

    2016-01-01

    Full Text Available We compared the acute toxicity of nanosilica and polyacrylate/nanosilica instillation in Wistar rats (n=60. Exposure to nanosilica and polyacrylate/nanosilica showed a 30% mortality rate. When compared with saline-treated rats, animals in both exposure groups exhibited a significant reduction of PO2 (P<0.05 at both 24 and 72 hr. after exposure. Both exposure groups exhibited a significant reduction of neutrophils in arterial blood compared to saline controls (P<0.05 24 hr. after exposure. The levels of blood ALT and LDH in exposed groups were found to be significantly increased (P<0.05 24 hr. following exposure. The exposed groups exhibited various degrees of pleural effusion and pericardial effusion. Our findings indicated respiratory exposure to polyacrylate/nanosilica and nanosilica is likely to cause multiple organ toxicity.

  3. Stabilization of magnetorheological suspensions by polyacrylic acid polymers.

    Science.gov (United States)

    Viota, J L; de Vicente, J; Durán, J D G; Delgado, A V

    2005-04-15

    This work is devoted to the synthesis and stabilization of magnetorheological suspensions constituted by monodisperse micrometer-sized magnetite spheres in aqueous media. The electrical double-layer characteristics of the solid/liquid interface were studied in the absence and presence of adsorbed layers of high molecular weight polyacrylic acids (PAA; Carbopol). Since the Carbopol-covered particles can be thought of as "soft" colloids, Ohshima's theory was used to gain information of the surface potential and the charge density of the polymer layer. The effect of the pH of the solution on the double-layer characteristics is related to the different conformations of the adsorbed molecules provoked by the dissociation of the acrylic groups present in polymer molecules. The stability of the suspensions was experimentally studied for different pH and polymer concentrations, and in the absence or presence of a weak magnetic field applied. The stability of the suspensions was explained using the classical DLVO theory of colloidal stability extended to account for hydration, steric, and magnetic interactions between particles. Diagrams of potential energy vs interparticle distance show the predominant effect of steric, hydrophilic/hydrophobic, and magnetic interactions on the whole stability of the system. The best conditions to obtain stable suspensions were found when strong steric and hydrophilic repulsions hinder the coagulation between polymer-covered particles, simultaneously avoiding sedimentation by the thickening effect of the polymer solution. When a not too high molecular weight PAA was employed in a low concentration, the task of a long-time antisettling effect compatible with the desired magnetic response of the fluid was achieved. PMID:15780292

  4. Probing structure-antifouling activity relationships of polyacrylamides and polyacrylates.

    Science.gov (United States)

    Zhao, Chao; Zhao, Jun; Li, Xiaosi; Wu, Jiang; Chen, Shenfu; Chen, Qiang; Wang, Qiuming; Gong, Xiong; Li, Lingyan; Zheng, Jie

    2013-07-01

    We have synthesized two different polyacrylamide polymers with amide groups (polySBAA and polyHEAA) and two corresponding polyacrylate polymers without amide groups (polySBMA and polyHEA), with particular attention to the evaluation of the effect of amide group on the hydration and antifouling ability of these systems using both computational and experimental approaches. The influence of polymer architectures of brushes, hydrogels, and nanogels, prepared by different polymerization methods, on antifouling performance is also studied. SPR and ELISA data reveal that all polymers exhibit excellent antifouling ability to repel proteins from undiluted human blood serum/plasma, and such antifouling ability can be further enhanced by presenting amide groups in polySBAA and polyHEAA as compared to polySBMA and polyHEA. The antifouling performance is positively correlated with the hydration properties. Simulations confirm that four polymers indeed have different hydration characteristics, while all presenting a strong hydration overall. Integration of amide group with pendant hydroxyl or sulfobetaine group in polymer backbones is found to increase their surface hydration of polymer chains and thus to improve their antifouling ability. Importantly, we present a proof-of-concept experiment to synthesize polySBAA nanogels, which show a switchable property between antifouling and pH-responsive functions driven by acid-base conditions, while still maintaining high stability in undiluted fetal bovine serum and minimal toxicity to cultured cells. This work provides important structural insights into how very subtle structural changes in polymers can yield great improvement in biological activity, specifically the inclusion of amide group in polymer backbone/sidechain enables to obtain antifouling materials with better performance for biomedical applications. PMID:23562049

  5. Effects of an AMPS-modifi ed Polyacrylic Acid Superplasticizer on the Performance of Concrete Materials

    Institute of Scientific and Technical Information of China (English)

    CHEN Baofan

    2015-01-01

    A self-made 2-acrylamide-2-methyl propylene sulfonic (AMPS)-modified polyacrylic acid superplasticizer and two other commercially available superplasticizers with different molecular structures are used in this study to investigate the effect of an AMPS-modifi ed polyacrylic acid superplasticizer on the properties of concrete materials. In the experiments, initial and 1.5 h slumps over time after admixtion are determined by adding different dosages of three superplasticizers into the premixed concrete to characterize the slump loss resistance of the premixed concrete. The water-reducing rates of three different types of concrete are determined to characterize the water-reducing capacity of the concrete with each superplasticizer. The 3, 7 and 28 d compressive strength is determined to characterize the mechanical properties of the concrete with each superplasticizer. In the meanwhile, 1, 1.5 and 2.0 h slump loss rates over time after admixtion are determined by adding different dosages of the three superplasticizers into the high-performance concrete (HPC) to characterize the slump loss resistance of HPC. The 7, 28, 60 and 90 d compressive strength is determined to characterize the compressive properties of HPC with each superplasticizer. The dry shrinkage rates of three different types of HPC are determined with each superplasticizer. Electricfl ux after standard curing for 56 d and chloride ion diffusion coeffi cient after curing for 28 d of HPC are determined to characterize the impermeability of HPC with each superplasticizer. The cross-section was examined using a scanning electron microscopy (SEM) system. Results demonstrate that the AMPS-modifi ed polyacrylic acid superplasticizer has better water-reducing effect and slump than the two commercially available polyacrylic acid superplasticizers. The AMPS-modifi ed polyacrylic acid superplasticizer also shows signifi cant improvement of the compressive strength, especially in comprehensive performance of HPC. In

  6. Synthesis, characterization and degradation behavior of admicelled polyacrylate-natural rubber

    International Nuclear Information System (INIS)

    In order to improve weatherability of the cured natural rubber, the novel introduction of good ozone resistant polymers such as polyacrylates (poly(methyl acrylate) (PMA) or poly(methyl methacrylate) (PMMA)) into natural rubber (NR) by admicellar polymerization was investigated in this work. The admicellar polymerization to synthesize polyacrylate layer over the surface of NR latex particles was performed with varying monomer type (PMA and PMMA) and content (50 and 100 mM). The admicelled PMMA showed higher molecular weight than PMA. Fourier transform infrared spectra of the admicellar synthesized natural rubbers exhibited characteristic peaks of those polyacrylates. Micrographs from transmission electron and field emission scanning electron microscopes (FE-SEM) revealed the coatings of PMA and PMMA over the rubber particles, suggesting a core-shell structure. Thermogravimetric analysis revealed that the admicelled rubbers not only showed an improvement in heat stability but also a single decomposition temperature. After vulcanization, FE-SEM results showed the cured admicelled rubbers had phase transformation from core-shell to phase separation (aggregate domains of polyacrylate-rich phase) with smooth interface. This agreed well to their one glass transition temperature (∼−48 °C) which indicated good miscibility between NR and each polyacrylate. The cracks generated after exposure to ozone found in the admicelled rubbers were smaller than those in NR, suggesting better ozone resistance was achieved. Increasing monomer concentration led to less cracks or much better ozone resistance. Furthermore, changes in mechanical properties after ozone exposure of the admicelled PMA-NR were less than those of the admicelled PMMA-NR (having the same shell content) and the NR, respectively. - Highlights: • We use admicellar technique to add polyacrylates to NR in form of core-shell rubber. • This core-shell structure was physically formed as seen by the phase

  7. Synthesis, characterization and degradation behavior of admicelled polyacrylate-natural rubber

    Energy Technology Data Exchange (ETDEWEB)

    Pongpilaipruet, Angkana; Magaraphan, Rathanawan, E-mail: rathanawan.k@chula.ac.th

    2015-06-15

    In order to improve weatherability of the cured natural rubber, the novel introduction of good ozone resistant polymers such as polyacrylates (poly(methyl acrylate) (PMA) or poly(methyl methacrylate) (PMMA)) into natural rubber (NR) by admicellar polymerization was investigated in this work. The admicellar polymerization to synthesize polyacrylate layer over the surface of NR latex particles was performed with varying monomer type (PMA and PMMA) and content (50 and 100 mM). The admicelled PMMA showed higher molecular weight than PMA. Fourier transform infrared spectra of the admicellar synthesized natural rubbers exhibited characteristic peaks of those polyacrylates. Micrographs from transmission electron and field emission scanning electron microscopes (FE-SEM) revealed the coatings of PMA and PMMA over the rubber particles, suggesting a core-shell structure. Thermogravimetric analysis revealed that the admicelled rubbers not only showed an improvement in heat stability but also a single decomposition temperature. After vulcanization, FE-SEM results showed the cured admicelled rubbers had phase transformation from core-shell to phase separation (aggregate domains of polyacrylate-rich phase) with smooth interface. This agreed well to their one glass transition temperature (∼−48 °C) which indicated good miscibility between NR and each polyacrylate. The cracks generated after exposure to ozone found in the admicelled rubbers were smaller than those in NR, suggesting better ozone resistance was achieved. Increasing monomer concentration led to less cracks or much better ozone resistance. Furthermore, changes in mechanical properties after ozone exposure of the admicelled PMA-NR were less than those of the admicelled PMMA-NR (having the same shell content) and the NR, respectively. - Highlights: • We use admicellar technique to add polyacrylates to NR in form of core-shell rubber. • This core-shell structure was physically formed as seen by the phase

  8. Preparation of Polyacrylate-based Conductive Coatings and Its PTC Effect

    Institute of Scientific and Technical Information of China (English)

    XIONG Chuan-xi; HU Hui-rong; ZHOU Zhi-yong; ZHANG Yi; DONG Li-jie

    2004-01-01

    Polyacrylate- based conductive coatings were prepared from polyacrylate emulsion as matrix andcarbon black (CB) whose surface was treated with titanate coupling agent as conducting particles. One kind oforganic crystal was added to study its effects on the electrical conductivity and PTC ( positive temperature coeffi-cient ) effect of the conductive coatings. Experimental results show that the coatings containing only polyacrylateemulsion and CB exhibit an excellent electrical conductivity but bad PTC effect, and when organic crystal is added,PTC effect is characterized and can increase by 2 orders of magtitude. The critical transformation temperature ofpolyacrylate emulsion/CB PTC composites is decided by melting point of organic crystals.

  9. Azo···phenyl stacking: a persistent self-assembly motif guides the assembly of fluorinated cis-azobenzenes into photo-mechanical needle crystals.

    Science.gov (United States)

    Bushuyev, Oleksandr S; Tomberg, Anna; Vinden, Joanna R; Moitessier, Nicolas; Barrett, Christopher J; Friščić, Tomislav

    2016-02-01

    We describe a novel, persistent motif of molecular assembly in photo-mechanical crystals and cocrystals of fluorinated cis-azobenzenes. The azo···phenyl stacking, preserved upon either chemical substitution or halogen-bonded cocrystallization, guides the assembly of fluorinated cis-azobenzenes into columnar stacks and drives the formation of crystals with needle-like morphologies optimal for photo-mechanical motion. PMID:26691226

  10. Poly(esterimide) bearing azobenzene units as photoaligning layer for liquid crystals

    Science.gov (United States)

    Węgłowski, Rafał; Piecek, Wiktor; Kozanecka-Szmigiel, Anna; Konieczkowska, Jolanta; Schab-Balcerzak, Ewa

    2015-11-01

    The custom synthesized azobenzene side-chain poly(esterimide) was used as an aligning material for nematic liquid crystal molecules. The anisotropy of the poly(esterimide) layer was generated by a linearly polarized UV light, as a consequence of multiple trans-cis-trans isomerization cycles. The photoalignment effect was studied by assembling a twisted nematic cell with a proper liquid crystal mixture and geometry to fulfill Mauguin's limit. The polarizing microscope pictures of the fabricated cells confirmed the twisted arrangement of liquid crystal molecules. The results of electro-optic measurements indicated a stronger anchoring of the liquid crystal molecules by photoaligned poly(esterimide) than that obtained in the case of a rubbed polyimide.

  11. Near-field lithography on the azobenzene polymer liquid crystal films

    Institute of Scientific and Technical Information of China (English)

    Douguo Zhang; Jian Liu; Zebo Zhang; Li Cao; Anlian Pan; Pei Wang; Yonghua Lu; Ming Bai; Jun Yang; Lin Tang; Jiangying Zhang; Hai Ming; Qijin Zhang

    2005-01-01

    @@ In this article, we reported near-field research on azobenzene polymer liquid crystal films using scanning near-field optical microscopy (SNOM). Optical writing and subsequently topographic reading of the patterns with subwavelength resolution were carried out in our experiments. Nanometer scale dots and lines were successfully fabricated on the films and the smallest dot diameter is about 120 nm. The width of the line fabricated is about 250 nm. This method is also a choice for nanolithography. The mechanism of the surface deformation on the polymer films was briefly analyzed from the viewpoint of gradient force in the optical near field. The intensity distribution of the electric field near the tip aperture was numerically simulated using finite-difference time-domain (FDTD) method and the numerical simulation results were consistent with the experimental results.

  12. Synthesis of photoresponsive cholesterol-based azobenzene organogels: dependence on different spacer lengths.

    Science.gov (United States)

    Ren, Yuchun; Wang, Bin; Zhang, Xiuqing

    2015-01-01

    A series of azobenzene-cholesterol organogel compounds (M 0 -M 12 ) with different spacers were designed and synthesized. The molecular structures were confirmed by (1)H NMR and (13)C NMR spectroscopy. The rapid and reversible photoresponsive properties of the compounds were investigated by UV-vis spectroscopy. Their thermal phase behaviors were studied by DSC. The length of the spacer plays a crucial role in the gelation. Compound M 6 is the only one that can gelate in ethanol, isopropanol and 1-butanol and the reversible gel-sol transitions are also investigated. To obtain visual insight into the microstructure of the gels, the typical structures of the xerogels were studied by SEM. Morphologies of the aggregates change from flower-like, network and rod with different sizes. By using IR and XRD characterization, it is found that intermolecular H-bonding, the solvents and van der Waals interaction are the main contributions to the specific superstructure. PMID:26199664

  13. MORPHOLOGY STUDY OF A SERIES OF AZOBENZENE-CONTAINING SIDE-ON LIQUID CRYSTALLINE TRIBLOCK COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    Wei Deng; Annie Br(u)let; Pierre-antoine Albouy; Patrick Keller; Xiao-gong Wang; Min-hui Li

    2012-01-01

    A series of azobenzene containing side-on liquid crystalline ABA triblock copolymers were investigated.This triblock series possesses the same central liquid crystal block B and various lengths of the amorphous block A.Transmission electron microscopy (TEM),small angle X-rays and neutron scattering (SAXS and SANS) were used to study their morphologies.Aider annealing the samples over weeks at a temperature within the nematic temperature range of block B,different morphologies (disordered,lamellar,perforated layer and hexagonal cylinder) were observed by TEM.The alignment behavior of these azo triblock copolymers in the magnetic field for artificial muscle application,as well as the phase period and the order-disorder transition (ODT) were studied in situ by SANS.

  14. High diffraction efficiency polarization gratings recorded by biphotonic holography in an azobenzene liquid crystalline polyester

    International Nuclear Information System (INIS)

    High diffraction efficiencies have been achieved with polarization gratings recorded in thin films of an azobenzene side-chain liquid crystalline polyester by means of biphotonic processes. Efficiency values up to 30% have been reached after an induction period of 300 s and subsequent evolution with the sample in darkness. These values are at least two orders of magnitude higher than those previously reported for biphotonic recording. The gratings can be erased with unpolarized blue light and partial recovery of the diffraction efficiency has been observed after the erasure process when the sample is kept in darkness. Red light illumination of the erased film increases the recovered efficiency value and the recovery rate. [copyright] 2001 American Institute of Physics

  15. Photoinduced optical anisotropy in azobenzene methacrylate block copolymers: Influence of molecular weight and irradiation conditions

    DEFF Research Database (Denmark)

    Gimeno, Sofia; Forcen, Patricia; Oriol, Luis;

    2009-01-01

    The photoinduced anisotropy in a series of azomethacrylate block copolymers with different Molecular weights and azo contents has been investigated under several irradiation conditions. Depending on molecular weight and composition, different microstructures (disordered, lamellar, spherical) appear...... the copolymers in which azobenzene units segregate to nano spheres and the lowest (and less stable) Delta n(N) values, appear in disordered systems not showing any defined microstructure. Besides, higher Delta n(N) is obtained in the copolymers with larger molecular weight of the poly (methyl......) and light power (from 100 to 500 mW/cm(2)) also influence the photoinduced response. Photoinduced Delta n(N) growth rate is faster when both temperature and irradiation power increase. Furthermore, birefringence is only induced at temperatures up to 90 degrees C, the maximum value being obtained at...

  16. Research progress of preparation of polyaniline/polyacrylic(polyacrylate) composites%聚苯胺/聚丙烯酸(酯)复合材料制备方法研究进展

    Institute of Scientific and Technical Information of China (English)

    李玉峰; 高晓辉; 祝晶晶; 童丽萍; 樊丽权

    2015-01-01

    Polyaniline/polyacrylic(polyacrylate) composites possess excellent performance of processibility,film-forming properties,adhesion,electrical properties and anti-corrosion properties. In this paper,the research on polyaniline/polyacrylic(polyacrylate) blend composites and polyaniline/polyacrylic (polyacrylate) polymerization composites at home and abroad is reviewed. The preparation methods , properties and applications of various kinds of polyaniline/polyacrylic(polyacrylate) composites are presented. The advantages and disadvantages of these preparation methods are further compared. The blending method is simple and easy to control,so it has wide application. The polymerization method could combine polyaniline with polyacrylic(polyacrylate) at molecular level to improve comprehensive properties. The interpenetrating network polymerization method realizes compatibility of two different molecular chains by network interpenetrating. The paper proposes that composite polyaniline and polyacrylic(polyacrylate) at molecular level is the main development direction in the future.%聚苯胺/聚丙烯酸(酯)复合材料具有良好的可加工性、成膜性、附着力、电学性能以及防腐蚀性能。本文回顾了国内外在聚苯胺/聚丙烯酸(酯)混合复合材料和聚苯胺/聚丙烯酸(酯)聚合复合材料等方面的研究工作,介绍了各种聚苯胺/聚丙烯酸(酯)复合材料的制备方法、性能及应用,并比较了这些制备方法的优缺点。分析结果表明:混合复合法工艺简单、易于控制、适用范围广;聚合复合法将聚苯胺和聚丙烯酸(酯)在分子水平上结合,使聚苯胺和聚丙烯酸(酯)的优异性能得以综合发挥;而互穿网络聚合法通过网络互穿实现了两种差别较大的分子链的强制相溶。提出在分子水平上的复合是聚苯胺/聚丙烯酸(酯)复合材料研究的主要发展方向。

  17. Molecular Understanding and Structural-Based Design of Polyacrylamides and Polyacrylates as Antifouling Materials.

    Science.gov (United States)

    Chen, Hong; Zhao, Chao; Zhang, Mingzhen; Chen, Qiang; Ma, Jie; Zheng, Jie

    2016-04-12

    Design and synthesis of highly bioinert and biocompatible antifouling materials are crucial for a broad range of biomedical and engineering applications. Among antifouling materials, polyacrylamides and polyacrylates have proved so promising because of cheap raw materials, ease of synthesis and applicability, and abundant functional groups. The strong surface hydration and the high surface packing density of polyacrylamides and polyacrylates are considered to be the key contributors to their antifouling property. In this article, we review our studies on the design and synthesis of a series of polyacrylamides and polyacrylates with different molecular structures. These polymers can be fabricated into different architectural forms (brushes, nanoparticles, nanogels, and hydrogels), all of which are highly resistant to the attachment of proteins, cells, and bacteria. We find that small structural changes in the polymers can lead to large enhancement in surface hydration and antifouling performance, both showing a positive correlation. This reveals a general design rule for effective antifouling materials. Furthermore, polyacrylamides and polyacrylates are readily functionalized with other bioactive compounds to achieve different new multifunctionalities. PMID:26986442

  18. FTIR-ATR Monitoring and SEC/RI/MALLS characterization of ATRP synthesized hyperbranched polyacrylates

    OpenAIRE

    Gonçalves, Miguel; Costa, Mário Rui; Dias, Rolando

    2009-01-01

    This work reports the synthesis at 1 L scale of hyperbranched polyacrylates based upon acrylate/diacrylate monomers such as n-butyl acrylate (nBA)/1,6-hexanediol diacrylate (HDDA) and using atom transfer radical polymerization (ATRP). A FTIR-ATR immersion probe was used to monitor the polymerization reaction. FCT

  19. Small Angle Neutron Scattering experiments on “side-on fixed"" liquid crystal polyacrylates

    OpenAIRE

    Leroux, N.; Keller, P.; Achard, M.; Noirez, L.; Hardouin, F.

    1993-01-01

    Small Angle Neutron Scattering experiments were carried out on liquid crystalline “side-on fixed” polyacrylates : we observe that the polymer backbone adopts a prolate conformation in the nematic phase. Such anisotropy of the global backbone is larger for smaller spacer length. In every case we measure at low temperatures a large chain extension as previously described in polysiloxanes.

  20. Mucolysis of the colonic mucus barrier by faecal proteinases: inhibition by interacting polyacrylate.

    Science.gov (United States)

    Hutton, D A; Pearson, J P; Allen, A; Foster, S N

    1990-03-01

    1. Mucolytic (mucus solubilizing) activity in human faeces has been characterized with both purified human and pig colonic mucin and shown to be mediated by proteolysis. 2. Mucolytic activity was demonstrated by: (i) a drop in mucin viscosity; (ii) a substantial reduction in mucin size, from polymer to degraded subunit, as assessed by Sepharose CL-2B gel filtration; (iii) formation of new N-terminal peptides. 3. Mucolytic activity was also followed in faecal extracts by its proteolytic activity using standard succinyl albumin substrate. Proteolysis extended over the pH range 4.5-11.0. Proteolysis was inhibited at pH 7.5 by soybean trypsin inhibitor and phenylmethanesulphonyl fluoride, suggesting the presence of serine proteinases. 4. The polyacrylate carbomer (934P) inhibited both mucolysis of pig colonic mucin and proteolysis of succinyl albumin. 5. Interaction between the polyacrylate (carbomer 934P) and purified human and pig colonic mucin was demonstrated by a marked synergistic increase in solution viscosity (360% above control). 6. The results demonstrate the presence of a mucolytic activity in the human colonic lumen that has the potential to degrade the mucus barrier, and that polyacrylates inhibit this mucolysis and interact to strengthen the colonic mucus barrier. Polyacrylates may therefore have therapeutic potential in inflammatory bowel disease where luminal proteolytic activity can be raised. PMID:2156646

  1. UV gelation of single-component polyacrylates bearing dinitrobenzoate side groups.

    Science.gov (United States)

    Xie, Tongqing; Yang, Li; Sun, Xingxing; Jiang, Jun; Zhang, Xuepeng; Luo, Yi; Zhang, Guoqing

    2016-07-19

    Polyacrylates bearing dinitrobenzoate side groups undergo sol-gel-sol transformations in DMF or THF solutions regulated by alternating UV light and dark conditions. The formation and recombination of radical ionic species via photoinduced electron transfer may be responsible. PMID:27373563

  2. Controlled formation of ag nanoparticles by means of long-chain sodium polyacrylates in dilute solution.

    Science.gov (United States)

    Huber, Klaus; Witte, Thomas; Hollmann, Jutta; Keuker-Baumann, Susanne

    2007-02-01

    A new tool is presented to control formation of Ag nanoparticles. Small amounts of silver ions were added to dilute solutions of long-chain sodium polyacrylates (NaPA). Four NaPA samples covering a molar mass regime of 97 kD polyacrylate coils toward compact structures. Coil shrinking and aggregation was revealed by means of time-resolved static light scattering. If exposed to UV-radiation, small Ag particles formed within the shrunken anionic polyacrylate coils. The Ag nanoparticles were identified by means of an enhanced light scattering and a characteristic plasmon absorption band around 410 nm. No such Ag particle formation could be observed even at 5 times larger concentrations of Ag(+) and NaPA if the two smallest polyacrylate samples have been used under otherwise equal conditions. This molar mass sensitive response of NaPA to Ag(+)-addition suggests an interesting phenomenon: if the coil size of the NaPa chains, which act as Ag(+) collectors, is large enough, local Ag(+) concentration in these coil-shaped Ag(+) containers exceeds a critical value, and irradiation with UV generates Ag nanoparticles. PMID:17263389

  3. Synthetic gene involving azobenzene-tethered T7 promoter for the photocontrol of gene expression by visible light.

    Science.gov (United States)

    Kamiya, Yukiko; Takagi, Toshiki; Ooi, Hideaki; Ito, Hiroshi; Liang, Xingguo; Asanuma, Hiroyuki

    2015-04-17

    In the present study, we demonstrate photoregulation of gene expression in a cell-free translation system from a T7 promoter containing two azobenzene derivatives at specific positions. As photoswitches, we prepared azobenzene-4'-carboxlyic acid (Azo) and 2,6-dimethylazobenzene-4'-carboxylic acid (DM-Azo), which were isomerized from trans to cis upon irradiation with UV light (λ protein from a promoter modified with S-Azo or S-DM-Azo could be induced by harmless visible light whereas that from a promoter modified with Azo or DM-Azo was induced only by UV light (340-360 nm). Thus, efficient photoregulation of green fluorescent protein production was achieved in a cell-free translation system with visible light without photodamage. PMID:25144622

  4. Spectroscopic enhancement in nanoparticles embedded glasses

    International Nuclear Information System (INIS)

    This presentation provides an overview of the recent progress in the enhancement of the spectroscopic characteristics of the glass embedded with nanoparticles (NPs). Some of our research activities with few significantly new results are highlighted and facilely analyzed. The science and technology dealing with the manipulation of the physical properties of rare earth doped inorganic glasses by embedding metallic NPs or nanoclusters produce the so-called 'nanoglass'. Meanwhile, the spectroscopic enhancement relates the intensity of the luminescence measured at certain transition. The enhancement which expectedly due to the 'plasmonics wave' (referring to the coherent coupling of photons to free electron oscillations called plasmon) occurs at the interface between a conductor and a dielectric. Plasmonics being an emerging concept in advanced optical material of nanophotonics has given this material the ability to exploit the optical response at nanoscale and opened up a new avenue in metal-based glass optics. There is a vast array of plasmonic NPs concepts yet to be explored, with applications spanning solar cells, (bio) sensing, communications, lasers, solid-state lighting, waveguides, imaging, optical data transfer, display and even bio-medicine. Localized surface plasmon resonance (LSPR) can enhance the optical response of nanoglass by orders of magnitude as observed. The luminescence enhancement and surface enhanced Raman scattering (SERS) are new paradigm of research. The enhancement of luminescence due to the influence of metallic NPs is the recurring theme of this paper

  5. Spectroscopic enhancement in nanoparticles embedded glasses

    Science.gov (United States)

    Sahar, M. R.; Ghoshal, S. K.

    2014-09-01

    This presentation provides an overview of the recent progress in the enhancement of the spectroscopic characteristics of the glass embedded with nanoparticles (NPs). Some of our research activities with few significantly new results are highlighted and facilely analyzed. The science and technology dealing with the manipulation of the physical properties of rare earth doped inorganic glasses by embedding metallic NPs or nanoclusters produce the so-called 'nanoglass'. Meanwhile, the spectroscopic enhancement relates the intensity of the luminescence measured at certain transition. The enhancement which expectedly due to the 'plasmonics wave' (referring to the coherent coupling of photons to free electron oscillations called plasmon) occurs at the interface between a conductor and a dielectric. Plasmonics being an emerging concept in advanced optical material of nanophotonics has given this material the ability to exploit the optical response at nanoscale and opened up a new avenue in metal-based glass optics. There is a vast array of plasmonic NPs concepts yet to be explored, with applications spanning solar cells, (bio) sensing, communications, lasers, solid-state lighting, waveguides, imaging, optical data transfer, display and even bio-medicine. Localized surface plasmon resonance (LSPR) can enhance the optical response of nanoglass by orders of magnitude as observed. The luminescence enhancement and surface enhanced Raman scattering (SERS) are new paradigm of research. The enhancement of luminescence due to the influence of metallic NPs is the recurring theme of this paper.

  6. Spectroscopic enhancement in nanoparticles embedded glasses

    Energy Technology Data Exchange (ETDEWEB)

    Sahar, M. R., E-mail: mrahim057@gmail.com; Ghoshal, S. K., E-mail: mrahim057@gmail.com [Advanced Optical Material Research Group, Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, 81310, Skudai, Johor Bahru, Johor (Malaysia)

    2014-09-25

    This presentation provides an overview of the recent progress in the enhancement of the spectroscopic characteristics of the glass embedded with nanoparticles (NPs). Some of our research activities with few significantly new results are highlighted and facilely analyzed. The science and technology dealing with the manipulation of the physical properties of rare earth doped inorganic glasses by embedding metallic NPs or nanoclusters produce the so-called 'nanoglass'. Meanwhile, the spectroscopic enhancement relates the intensity of the luminescence measured at certain transition. The enhancement which expectedly due to the 'plasmonics wave' (referring to the coherent coupling of photons to free electron oscillations called plasmon) occurs at the interface between a conductor and a dielectric. Plasmonics being an emerging concept in advanced optical material of nanophotonics has given this material the ability to exploit the optical response at nanoscale and opened up a new avenue in metal-based glass optics. There is a vast array of plasmonic NPs concepts yet to be explored, with applications spanning solar cells, (bio) sensing, communications, lasers, solid-state lighting, waveguides, imaging, optical data transfer, display and even bio-medicine. Localized surface plasmon resonance (LSPR) can enhance the optical response of nanoglass by orders of magnitude as observed. The luminescence enhancement and surface enhanced Raman scattering (SERS) are new paradigm of research. The enhancement of luminescence due to the influence of metallic NPs is the recurring theme of this paper.

  7. Magnetite nanoparticles embedded in biodegradable porous silicon

    Energy Technology Data Exchange (ETDEWEB)

    Granitzer, P., E-mail: petra.granitzer@uni-graz.a [Institute of Physics, Karl Franzens University Graz, Universitaetsplatz 5, 8010 Graz (Austria); Institute for Electron Microscopy, University of Technology Graz, Steyrergasse 17, 8010 Graz (Austria); Rumpf, K. [Institute of Physics, Karl Franzens University Graz, Universitaetsplatz 5, 8010 Graz (Austria); Roca, A.G.; Morales, M.P. [Instituto de Ciencia de Materiales de Madrid, CSIC, Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain); Poelt, P.; Albu, M. [Institute for Electron Microscopy, University of Technology Graz, Steyrergasse 17, 8010 Graz (Austria)

    2010-05-15

    Magnetite nanoparticles, which are coated with oleic acid in a hexane solution and exhibit an average diameter of 7.7 nm, were embedded in a porous silicon (PS) matrix by immersion under defined parameters (e.g. concentration, temperature, time). The porous silicon matrix is prepared by anodization of a highly n-doped silicon wafer in an aqueous HF-solution. Magnetic characterization of the samples has been performed by SQUID-magnetometry. The superparamagnetic behaviour of the magnetite nanoparticles is represented by temperature-dependent magnetization measurements. Zero field (ZFC)/field cooled (FC) experiments indicate magnetic interactions between the particles. For the infiltration into the PS-templates different concentrations of the magnetite nanoparticles are used and magnetization measurements are performed in respect with magnetic interactions between the particles. The achieved porous silicon/magnetite specimens are not only interesting due to their transition between superparamagnetic and ferromagnetic behaviour, and thus for magnetic applications but also because of the non-toxicity of both materials giving the opportunity to employ the system in medical applications as drug delivery or in medical diagnostics.

  8. Magnetite nanoparticles embedded in biodegradable porous silicon

    International Nuclear Information System (INIS)

    Magnetite nanoparticles, which are coated with oleic acid in a hexane solution and exhibit an average diameter of 7.7 nm, were embedded in a porous silicon (PS) matrix by immersion under defined parameters (e.g. concentration, temperature, time). The porous silicon matrix is prepared by anodization of a highly n-doped silicon wafer in an aqueous HF-solution. Magnetic characterization of the samples has been performed by SQUID-magnetometry. The superparamagnetic behaviour of the magnetite nanoparticles is represented by temperature-dependent magnetization measurements. Zero field (ZFC)/field cooled (FC) experiments indicate magnetic interactions between the particles. For the infiltration into the PS-templates different concentrations of the magnetite nanoparticles are used and magnetization measurements are performed in respect with magnetic interactions between the particles. The achieved porous silicon/magnetite specimens are not only interesting due to their transition between superparamagnetic and ferromagnetic behaviour, and thus for magnetic applications but also because of the non-toxicity of both materials giving the opportunity to employ the system in medical applications as drug delivery or in medical diagnostics.

  9. The effect of photoisomerization on the enzymatic hydrolysis of polymeric micelles bearing photo-responsive azobenzene groups at their cores.

    Science.gov (United States)

    Harnoy, Assaf J; Slor, Gadi; Tirosh, Einat; Amir, Roey J

    2016-06-28

    The design of stable polymeric micelles that can respond to specific stimuli is crucial for the development of smart micellar nanocarriers that can release their active cargo selectively at the target site, thus diminishing the therapeutic limitations due to non-selective damage to healthy tissues. Here we report the design and synthesis of photo- and enzyme-responsive amphiphilic PEG-dendron hybrids bearing one, two or four enzymatically cleavable azobenzene end-groups. These dual-responsive hybrids can respond to light through the reversible isomerization of the azobenzene end-groups from the non-polar trans isomer to the highly polar cis isomer and vice versa, upon UV and visible irradiation, respectively. The high structural precision of these hybrids, which emerges from the dendritic architecture, enabled a detailed study of the photoisomerization of the azobenzene end-groups with high molecular resolution. Remarkably, although the transition from trans-to-cis led to a significant increase in the polarity of the micellar cores, the micelles remained stable. Our kinetic studies show that although the trans isomer is a better substrate for the activating enzyme, the UV induced formation of the cis azobenzene end-groups led to significant acceleration of the enzymatic hydrolysis of the end-groups. These results provide strong indication that the enzyme cannot reach the core of the micelles and instead the end-groups have to leave the hydrophobic core in order to be exposed on the micelle's surface or even leave the micelle in order to allow their cleavage by the activating enzymes. PMID:27093537

  10. Luminescence and Magnetic Properties of Two Three -Dimensional Terbium and Dysprosium MOFs Based on Azobenzene-4,4 '-Dicarboxylic Linker

    OpenAIRE

    Fernández, Belén; Oyarzabal Epelde, Itziar; Seco Botana, José Manuel; San Sebastián Larzabal, Eider; Fairen-Jiménez, David; Gómez-Ruiz, Santiago; Salinas-Castillo, Alfonso; Calahorro, Antonio J.; Rodríguez-Diéguez, Antonio

    2016-01-01

    We report the in situ formation of two novel metal-organic frameworks based on terbium and dysprosium ions using azobenzene-4,4-dicarboxylic acid (H(2)abd) as ligand, synthesized by soft hydrothermal routes. Both materials show isostructural three-dimensional networks with channels along a axis and display intense photoluminescence properties in the solid state at room temperature. Textural properties of the metal-organic frameworks (MOFs) have been fully characterized although no appreciable...

  11. Asymmetric Dimers of Chiral Azobenzene Dopants Exhibiting Unusual Helical Twisting Power upon Photoswitching in Cholesteric Liquid Crystals.

    Science.gov (United States)

    Kim, Yuna; Tamaoki, Nobuyuki

    2016-02-01

    In this study, we synthesized asymmetric dimeric chiral molecules as photon-mode chiral switches for reversible tuning of self-assembled helical superstructures. The chiral switches bearing two mesogen units-cholesterol and azobenzene moieties connected through flexible alkylenedioxy bridges-were doped into nematic liquid crystals, resulting in a chiral nematic (cholesteric) phase. Under irradiation with UV light, photoisomerization of the azobenzene units led to unprecedented switching of the cholesteric pitch and helical twisting power (HTP, β), with a higher HTP found in the cis-rich state (bent-form) than in the trans-state (rod-form). We attribute this behavior to the elongated cybotactic smectic clusters disrupting the helical orientation of the molecules in the cholesteric liquid crystals; their reversible decay and reassembly was evidenced upon sequential irradiation with UV and visible light, respectively. In addition to the photoisomerization of the azobenzene units, the odd/even parity of the alkylenedioxy linkers of the dimeric dopants also had a dramatic effect on the transitions of the cybotactic smectic domains. On the basis of the large rotational reorganization of the cholesteric helix and HTP switching (Δβ/βini of up to 50%), we could control the macroscopic rotational motion of microsized glass rods upon irradiating the surface of a cholesteric liquid crystal film featuring a polygonal fingerprint texture using UV and visible light. PMID:26815738

  12. Surface hopping dynamics of direct trans → cis photoswitching of an azobenzene derivative in constrained adsorbate geometries.

    Science.gov (United States)

    Floß, Gereon; Granucci, Giovanni; Saalfrank, Peter

    2012-12-21

    With ongoing miniaturization of electronic devices, the need for individually addressable, switchable molecules arises. An example are azobenzenes on surfaces which have been shown to be switchable between trans and cis forms. Here, we examine the "direct" (rather than substrate-mediated) channel of the trans → cis photoisomerization after ππ∗ excitation of tetra-tert-butyl-azobenzene physisorbed on surfaces mimicking Au(111) and Bi(111), respectively. In spirit of the direct channel, the electronic structure of the surface is neglected, the latter merely acting as a rigid platform which weakly interacts with the molecule via Van-der-Waals forces. Starting from thermal ensembles which represent the trans-form, sudden excitations promote the molecules to ππ∗-excited states which are non-adiabatically coupled among themselves and to a nπ∗-excited and the ground state, respectively. After excitation, relaxation to the ground state by internal conversion takes place, possibly accompanied by isomerization. The process is described here by "on the fly" semiclassical surface hopping dynamics in conjunction with a semiempirical Hamiltonian (AM1) and configuration-interaction type methods. It is found that steric constraints imposed by the substrate lead to reduced but non-vanishing, trans → cis reaction yields and longer internal conversion times than for the isolated molecule. Implications for recent experiments for azobenzenes on surfaces are discussed. PMID:23267492

  13. NAA of ion exchanged sodium polyacrylate for monitoring air quality in the workplace

    International Nuclear Information System (INIS)

    Sodium polyacrylate is a superabsorbent polymer (SAP) which is widely used in the manufacturing of disposable diapers. Workplace exposure to respirable dust produced from the handling of these polymers is becoming more of a concern as more data relating occupational exposures to health effects are becoming available. An approach that utilizes the fundamental ion exchange properties of the polymer combined with the sensitivity of instrumental neutron activation analysis has been developed which eliminates interferences from sodium species that are ubiquitous to manufacturing facilities. The technique involves exchanging the sodium that is associated with the polymer with europium and analyzing the exchanged polymer by neutron activation analysis. The technique is simple to run, provides excellent sensitivity and is specific to sodium polyacrylate. (author)

  14. Research on various factors influencing the moisture absorption property of sodium polyacrylate

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Sodium polyacrylate was synthesized with acrylic acid as the monomer, and sodium bisulfate and ammonium persulfate as the initiator, by means of aqueous solution polymerization. The factors influencing the properties of moisture absorption, such as monomer concentration, dosage of initiator, and reaction temperature were systematically investigated. The experimental results indicate that the moisture-absorbing property of this polymer was better than other traditional material, such as silica gel, and molecular sieve. The best reaction condition and formula are based on the orthogonal experiment design. The optimum moisture absorbency of sodium polyacrylate reaches 1.01 g/g. The mathematical correlation of this polymer with various factors and moisture absorbency is obtained based on the multiple regression analysis. The moisture content intuitive analysis table shows that neutralization degree has the most significant influence on moisture absorbency, followed by monomer concentration and reaction temperature, while other factors have less influence.

  15. SYNTHESIS, CROSSLINKING MECHANISM AND PROPERTIES OF A POLYACRYLATE/POLYURETHANE COMPOSITE COATING

    Institute of Scientific and Technical Information of China (English)

    TANG Liming; GUO Wei; ZHOU Qixiang

    1997-01-01

    A polyacrylate/polyurethane (P(A)/P(U)) composite coating has been prepared by crosslinking an acetoacetylated polyacrylate with a vinylic group terminated polyurethane at room temperature. A model Michael reaction between ethyl acetoacetate (EAA) and methyl acrylate (MA) was designed to study the crosslinking mechanism. It was found that the two active hydrogen atoms in acetoacetyl group can both add to vinylic groups and the yield of mono- and bis-adducts are much affected by the molar ratio of acetoacetyl to vinylic groups. Higher crosslinking degree and better properties could be obtained with decreasing the molar ratio of the two active groups from 1/1 to 0.6/1 in the composite coatings.

  16. Protein partitioning in poly(ethylene glycol)/sodium polyacrylate aqueous two-phase systems.

    Science.gov (United States)

    Johansson, Hans-Olof; Magaldi, Flavio Musa; Feitosa, Eloi; Pessoa, Adalberto

    2008-01-18

    The partition of hemoglobin, lysozyme and glucose-6-phosphate dehydrogenase (G6PDH) in a novel inexpensive aqueous two-phase system (ATPS) composed by poly(ethylene glycol) (PEG) and sodium polyacrylate (NaPA) has been studied. The effect of NaCl and Na(2)SO(4), pH and PEG molecular size on the partitioning has been studied. At high pH (above 9), hemoglobin partitions strongly to the PEG-phase. Although some precipitation of hemoglobin occurs, high recovery values are obtained particularly for lysozyme and G6PDH. The partitioning forces are dominated by the hydrophobic and electrochemical (salt) effects, since the positively charged lysozyme and negatively charged G6PDH partitions to the non-charged PEG and the strongly negatively charged polyacrylate enriched phase, respectively. PMID:18078945

  17. Conjugation, characterization and toxicity of lipophosphoglycan-polyacrylic acid conjugate for vaccination against leishmaniasis

    OpenAIRE

    Topuzogullari, Murat; Cakir Koc, Rabia; Dincer Isoglu, Sevil; Bagirova, Melahat; Akdeste, Zeynep; Elcicek, Serhat; Oztel, Olga N.; Yesilkir Baydar, Serap; Canim Ates, Sezen; Allahverdiyev, Adil M

    2013-01-01

    Research on the conjugates of synthetic polyelectrolytes with antigenic molecules, such as proteins, peptides, or carbohydrates, is an attractive area due to their highly immunogenic character in comparison to classical adjuvants. For example, polyacrylic acid (PAA) is a weak polyelectrolyte and has been used in several biomedical applications such as immunological studies, drug delivery, and enzyme immobilization. However, to our knowledge, there are no studies that document immune-stimulant...

  18. Evidence of Hydrogen Bonding in Chloroform and Polyacrylates from NMR Measurements

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The presence of hydrogen bonding in chloroform and polyacrylate mixtures was demonstrated by observation of 1H- and 13C-NMR chemical shifts. Comparison of the nuclear magnetic resonance (NMR) chemical shift in polymer solutions with their low molecular mass analogues showed the effect of steric hindrance on hydrogen bonding. This initial investigation is helpful for understanding the intermolecular interaction in relatively weak hydrogen bonding polymer solutions.

  19. Comparison of finishing application for aliphatic polyurethane dispersions and polyurethane/polyacrylate composite emulsions

    OpenAIRE

    Chai, S; Zhang, Zhongyi

    2010-01-01

    Aliphatic and aromatic cationic aqueous polyurethane (PU-1, PU-2), aliphatic anionic aqueous polyurethanes (PU-3, PU-4) were prepared with polyether glycol, polyether polyol, toluene diisocyanate and isophorone diisocyanate as raw materials. The core-shell polyurethane/polyacrylate composite emulsions (PUA-5, PUA-6) as well as interpenetrating PUA composite emulsions (PUA-7,PUA-8) were prepared by seeded emulsion polymerization, the aliphatic anionic aqueous PU dispersions were used as seed p...

  20. IN SITU INTERFEROMETRIC STUDY ON THE GELATION PROCESS OF POLYACRYLIC ACID GELS

    Institute of Scientific and Technical Information of China (English)

    Ying Guan; Qiang Chen; Xian-min Zhang; Yu-xing Peng; Jian Xu

    2000-01-01

    In situ interferometry was used to investigate the gelation process of polyacrylic acid (PAA) gels. The basic principle of the in situ interferometry technique is illustrated. It can give sufficient information for non-destructive and successful investigation of the whole gelation process. The effect of initiator concentration on the gelation process was studied. The polymerization rate of AA increases with increasing initiator concentration. The error arising from the thermal effect in the gelation process can be neglected.

  1. Characterization and effects of cross-linked potassium polyacrylate as soil amendment

    OpenAIRE

    Sanz Gómez, Jorge

    2016-01-01

    Falta palabras clave Cross-linked potassium polyacrylate (Luquasorb®1280R) is a granular anionic superabsorbent polymer with the ability to absorb large amounts of water. The objectives of this study were the physicochemical characterization of the material and its effects when used as soil amendment together with the evaluation of the impact on agronomical parameters when it was applied to processing varieties of tomato (Solanum lycopersicum L.) grown under Mediterranean climate condit...

  2. Synthesis and Properties of IPN Hydrogels Based on Konjac Glucomannan and Poly(acrylic acid)

    Institute of Scientific and Technical Information of China (English)

    Bing LIU; Zhi Lan LIU; Ren Xi ZHUO

    2006-01-01

    Novel interpenetrating polymer network (IPN) hydrogels based on konjac glucomannan (KGM) and poly(acrylic acid) (PAA) were prepared by polymerization and cross-linking of acrylic acid (AA) in the pre-fabricated KGM gel. The IPN gel was analyzed by FT-IR. The studies on the equilibrium swelling ratio of IPN hydrogels revealed their sensitive response to environmental pH value. The results of in vitro degradation showed that the IPN hydrogels retain the enzymatic degradation character of KGM.

  3. Effects of sodium polyacrylate on water retention and infiltration capacity of a sandy soil

    OpenAIRE

    Zhuang, Wenhua; Li, Longguo; Liu, Chao

    2013-01-01

    Based on the laboratory study, the effects of sodium polyacrylate (SP) was investigated at 5 rates of 0, 0.08, 0.2, 0.5, and 1%, on water retention, saturated hydraulic conductivity(Ks), infiltration characteristic and water distribution profiles of a sandy soil. The results showed that water retention and available water capacity effectively increased with increasing SP rate. The Ks and the rate of wetting front advance and infiltration under certain pond infiltration was significantly reduc...

  4. Antibiotic-Conjugated Polyacrylate Nanoparticles: New Opportunities for Development of Anti-MRSA Agents

    OpenAIRE

    Turos, Edward; Shim, Jeung-Yeop; Wang, Yang; Greenhalgh, Kerriann; Reddy, G. Suresh Kumar; Dickey, Sonja; Lim, Daniel V

    2006-01-01

    This report describes the preparation of polyacrylate nanoparticles in which an N-thiolated β-lactam antibiotic is covalently conjugated onto the polymer framework. These nanoparticles are formed in water by emulsion polymerization of an acrylated antibiotic pre-dissolved in a liquid acrylate monomer (or mixture of co-monomers) in the presence of sodium dodecyl sulfate as a surfactant and potassium persulfate as a radical initiator. Dynamic light scattering analysis and electron microscopy im...

  5. Methods for Purifying and Detoxifying Sodium Dodecyl Sulfate-Stabilized Polyacrylate Nanoparticles

    OpenAIRE

    Garay-Jimenez, Julio C.; Young, Ashley; Gergeres, Danielle; Greenhalgh, Kerriann; Turos, Edward

    2008-01-01

    Recent research in our laboratory has centered on studies of polyacrylate and polyacrylamide nanoparticle emulsions for use in antibiotic delivery. Our goal is to develop these nanoparticle emulsions for treatment of life-threatening bacterial infections such as those caused by methicillin-resistant Staphylococcus aureus (MRSA). For this intended application, it is necessary to ensure that the biological activity of the emulsion is due only to the drug attached to the polymeric chain, rather ...

  6. Penicillin-Bound Polyacrylate Nanoparticles: Restoring the Activity of β-Lactam Antibiotics Against MRSA

    OpenAIRE

    Turos, Edward; Reddy, G. Suresh Kumar; Greenhalgh, Kerriann; Ramaraju, Praveen; Abeylath, Sampath C.; Jang, Seyoung; Dickey, Sonja; Lim, Daniel V

    2007-01-01

    This report describes the preparation of antibacterially-active emulsified polyacrylate nanoparticles in which a penicillin antibiotic is covalently conjugated onto the polymeric framework. These nanoparticles were prepared in water by emulsion polymerization of an acrylated penicillin analogue pre-dissolved in a 7:3 (w:w) mixture of butyl acrylate and styrene in the presence of sodium dodecyl sulfate (surfactant) and potassium persulfate (radical initiator). Dynamic light scattering analysis...

  7. Endoscopic treatment of vesicoureteral reflux with polyacrylate polyalcohol copolymer and dextranomer/hyaluronic acid in adults

    OpenAIRE

    Akif Turk; Ahmet Selimoglu; Kadir Demir; Osman Celik; Erkin Saglam; Fatih Tarhan

    2014-01-01

    Purpose Aim of this study is to examine the effectiveness of dextranomer/hyaluronic acid copolymer and polyacrylate polyalcohol copolymer in endoscopic treatment of vesicoureteral reflux disease in adult patients with and without chronic renal failure. Materials and Methods Thirty two patients (12 female, 20 male) with a total of 50 renal units were treated for vesicoureteral reflux. There were 26 (81%) chronic renal failure patients. The success of treatment was evaluated by voiding cyst...

  8. Optical storage in azobenzene-containing epoxy polymers processed as Langmuir Blodgett films

    Energy Technology Data Exchange (ETDEWEB)

    Fernández, Raquel; Mondragon, Iñaki [‘Materials - Technologies’ Group, Department of Chemical and Environmental Engineering, Polytechnic School, Universidad País Vasco/Euskal Herriko Unibertsitatea, Pza Europa 1, 20018 Donostia-San Sebastián (Spain); Sanfelice, Rafaela C.; Pavinatto, Felippe J.; Oliveira, Osvaldo N. [Instituto de Física de São Carlos, Universidade de São Paulo, Av. Trabalhador São Carlense, 400, Centro, CEP 13560-970, São Carlos (Brazil); Oyanguren, Patricia [Institute of Materials Science and Technology (INTEMA), University of Mar del Plata and National Research Council (CONICET), J. B. Justo 4302, 7600 Mar del Plata (Argentina); Galante, María J., E-mail: galant@fi.mdp.edu.ar [Institute of Materials Science and Technology (INTEMA), University of Mar del Plata and National Research Council (CONICET), J. B. Justo 4302, 7600 Mar del Plata (Argentina)

    2013-04-01

    In this study, azocopolymers containing different main-chain segments have been synthesized with diglycidyl ether of bisphenol A (DGEBA, DER 332, n = 0.03) and the azochromophore Disperse Orange 3 (DO3) cured with two monoamines, viz. benzylamine (BA) and m-toluidine (MT). The photoinduced birefringence was investigated in films produced with these azopolymers using the spin coating (SC) and Langmuir Blodgett (LB) techniques. In the LB films, birefringence increased with the content of azochromophore and the film thickness, as expected. The nanostructured nature of the LB films led to an enhanced birefringence and faster dynamics in the writing process, compared to the SC films. In summary, the combination of azocopolymers and the LB method may allow materials with tuned properties for various optical applications, including in biological systems were photoisomerization may be used to trigger actions such as drug delivery. Highlights: ► Langmuir Blodgett (LB) films of epoxy-based azopolymers were obtained and analyzed. ► Optical properties of LB and spin coated (SC) films were compared. ► Azo content, structure, laser power and number of layers were main factors studied. ► LB films had larger free volume for the azobenzenes isomerization than SC. ► LB films led to higher birefringence and faster dynamics compared to SC.

  9. Quantitative Structure-activity Relationships for Anaerobic Biodegradation of Substituted Azobenzenes

    Institute of Scientific and Technical Information of China (English)

    ZHANG Xiao-yi; ZHU Huai-wu; LUO Shi-xia; WANG Zheng-wu; XIAO Han

    2004-01-01

    The degradation rates of the azo-bonds of a series of substituted azobenzenes caused by anaerobic sludge digestion were determined by measuring the biggest change of the absorption peak area of the UV-Vis spectra of the anaerobic sludge system before and after degradation. The electronic structure of the molecules was calculated by using the quantum chemistry semiempirical method AM1. The research on the correlation between the biodegradability of the azo-bond and the molecular structure descriptors has led to the following results. (1) There is an obvious relationship between the degradation rate D and the difference Δqπ in π-charge density of the azo-bond. (2) The different substituents in the molecules result in a wave pattern of π-charge distribution and the increasing of the flowability of π-electron. A good flowability of the π-charge favors the reduction between electron contributing azo groups. (3) The effect of the substituents on the π-electron system depends on the electromerization of the substituents in combination with the conjugated systems.

  10. Study on the prediction of visible absorption maxima of azobenzene compounds

    Institute of Scientific and Technical Information of China (English)

    LIU Jun-na; CHEN Zhi-rong; YUAN Shen-feng

    2005-01-01

    The geometries of azobenzene compounds are optimized with B3LYP/6-311 G* method, and analyzed with nature bond orbital, then their visible absorption maxima are calculated with TD-DFT method and ZINDO/S method respectively. The results agree well with the observed values. It was found that for the calculation of visible absorption using ZINDO/S method could rapidly yield better results by adjusting OWFπ-π (the relationship between π-π overlap weighting factor) value than by the TD-DFT method. The method of regression showing the linear relationship between OWFπ-π and BLN-N (nitrogen-nitrogen bond lengths) as OWFπ-π=-8.1537+6.5638BLN-N, can be explained in terms of quantum theory, and also be used for prediction of visible absorption maxima of other azobenzne dyes in the same series. This study on molecules' orbital geometry indicates that their visible absorption maxima correspond to the electron transition from HOMO (the highest occupied molecular orbital) to LUMO (the lowest unoccupied molecular orbital).

  11. Photopatterned surface relief gratings in azobenzene-amorphous polycarbonate thin films

    Science.gov (United States)

    Vollmann, Morten; Getek, Peter; Olear, Kellie; Combs, Cody; Campos, Benjamin; Witkowski, Edmund; Cain, Erin; McGee, David

    Photoinduced orientation of azobenzene chromophores in polymeric host materials has been broadly explored for optical processing applications. Illumination of the chromophore with polarized light rotates the trans isomer perpendicular to the polarization, resulting in spatially modulated birefringence. The photoinduced anisotropy may also drive mass transport, with surface relief patterns being observed in a wide variety of systems. Here we report photoinduced birefringence in a guest-host system of Disperse Red 1- amorphous polycarbonate (DR1-APC). Birefringence was induced with a 490 nm laser and probed at 633 nm, with typical values of Δn = 0.01 in 2 micron thick films. Illumination of DR1-APC with intensity and/or polarization gratings also resulted in sinusoidal surface relief patterns with periodicity 1- 3 micron as controlled by the interbeam crossing angle of the 490 nm writing beams; the surface modulation was +/- 20 nm as measured by atomic force microscopy. Photopatterned DR1-APC is advantageous for applications given the ease of thin-film fabrication and the high glass transition temperature of APC, resulting in robust optically-induced surface gratings. We acknowledge support from NSF-DMR Award No. 1138416.

  12. Photocontrol of Voltage-Gated Ion Channel Activity by Azobenzene Trimethylammonium Bromide in Neonatal Rat Cardiomyocytes.

    Directory of Open Access Journals (Sweden)

    Sheyda R Frolova

    Full Text Available The ability of azobenzene trimethylammonium bromide (azoTAB to sensitize cardiac tissue excitability to light was recently reported. The dark, thermally relaxed trans- isomer of azoTAB suppressed spontaneous activity and excitation propagation speed, whereas the cis- isomer had no detectable effect on the electrical properties of cardiomyocyte monolayers. As the membrane potential of cardiac cells is mainly controlled by activity of voltage-gated ion channels, this study examined whether the sensitization effect of azoTAB was exerted primarily via the modulation of voltage-gated ion channel activity. The effects of trans- and cis- isomers of azoTAB on voltage-dependent sodium (INav, calcium (ICav, and potassium (IKv currents in isolated neonatal rat cardiomyocytes were investigated using the whole-cell patch-clamp technique. The experiments showed that azoTAB modulated ion currents, causing suppression of sodium (Na+ and calcium (Ca2+ currents and potentiation of net potassium (K+ currents. This finding confirms that azoTAB-effect on cardiac tissue excitability do indeed result from modulation of voltage-gated ion channels responsible for action potential.

  13. Fast photodynamics of azobenzene probed by scanning excited-state potential energy surfaces using slow spectroscopy.

    Science.gov (United States)

    Tan, Eric M M; Amirjalayer, Saeed; Smolarek, Szymon; Vdovin, Alexander; Zerbetto, Francesco; Buma, Wybren Jan

    2015-01-01

    Azobenzene, a versatile and polymorphic molecule, has been extensively and successfully used for photoswitching applications. The debate over its photoisomerization mechanism leveraged on the computational scrutiny with ever-increasing levels of theory. However, the most resolved absorption spectrum for the transition to S1(nπ*) has not followed the computational advances and is more than half a century old. Here, using jet-cooled molecular beam and multiphoton ionization techniques we report the first high-resolution spectra of S1(nπ*) and S2(ππ*). The photophysical characterization reveals directly the structural changes upon excitation and the timescales of dynamical processes. For S1(nπ*), we find that changes in the hybridization of the nitrogen atoms are the driving force that triggers isomerization. In combination with quantum chemical calculations we conclude that photoisomerization occurs along an inversion-assisted torsional pathway with a barrier of ~2 kcal mol(-1). This methodology can be extended to photoresponsive molecular systems so far deemed non-accessible to high-resolution spectroscopy. PMID:25562840

  14. Ultrafast vectorial and scalar dynamics of ionic clusters: Azobenzene solvated by oxygen

    Science.gov (United States)

    Paik, D. Hern; Baskin, J. Spencer; Kim, Nam Joon; Zewail, Ahmed H.

    2006-10-01

    The ultrafast dynamics of clusters of trans-azobenzene anion (A-) solvated by oxygen molecules was investigated using femtosecond time-resolved photoelectron spectroscopy. The time scale for stripping off all oxygen molecules from A- was determined by monitoring in real time the transient of the A- rise, following an 800nm excitation of A- (O2)n, where n =1-4. A careful analysis of the time-dependent photoelectron spectra strongly suggests that for n >1 a quasi-O4 core is formed and that the dissociation occurs by a bond cleavage between A- and conglomerated (O2)n rather than a stepwise evaporation of O2. With time and energy resolutions, we were able to capture the photoelectron signatures of transient species which instantaneously rise (rupture of the A--(O2)n nuclear coordinate and a slower component (1.6-36ps, increasing with n) attributed to an indirect channel exhibiting a quasistatistical behavior. The photodetachment transients exhibit a change in the transition dipole direction as a function of time delay. Rotational dephasing occurs on a time scale of 2-3ps, with a change in the sign of the transient anisotropy between A-O2 and the larger clusters. This behavior is a key indicator of an evolving cluster structure and is successfully modeled by calculations based on the structures and inertial motion of the parent clusters.

  15. POLYMER SCAFFOLDS BEARING AZOBENZENE —— POTENTIAL FOR OPTICAL INFORMATION STORAGE

    Institute of Scientific and Technical Information of China (English)

    Sφren Hvilsted; P.S. Ramanujam

    2001-01-01

    The fundamental optical storage mechanism of the laser light addressable azobenzene moiety is briefly introduced.A modular and flexible synthesis design furnishes polyester matrices covalently integrating cyanoazobenzene in regularly spaced side chains. Thin films of these materials are particularly well suited for holographic storage. Notable figures of merits of liquid crystalline polyesters are response time to blue-green laser light of the order of nanoseconds, storage capacity expressed as 5000 lines/mm, and high, permanent (almost nine years) diffraction efficiency of the order of 50% or greater,and erasability. The implications of the main chain nature for polyester morphology and for the permanency of the induced anisotropy are discussed. The design and methods of preparation of other significantly different polymer scaffolds supporting cyanoazobenzene are elaborated. Oligopeptides always result in amorphous materials, whereas copolymethacrylates and dendritic or hyperbranched polyesters provide some materials that exhibit liquid crystallinity. However, none of these scaffolds affords materials that result in permanent anisotropy when exposed to interfering laser light.

  16. Thermal and Electronic Fluctuations of Flexible Adsorbed Molecules: Azobenzene on Ag(111)

    Science.gov (United States)

    Maurer, Reinhard J.; Liu, Wei; Poltavsky, Igor; Stecher, Thomas; Oberhofer, Harald; Reuter, Karsten; Tkatchenko, Alexandre

    2016-04-01

    We investigate the thermal and electronic collective fluctuations that contribute to the finite-temperature adsorption properties of flexible adsorbates on surfaces on the example of the molecular switch azobenzene C12 H10 N2 on the Ag(111) surface. Using first-principles molecular dynamics simulations, we obtain the free energy of adsorption that accurately accounts for entropic contributions, whereas the inclusion of many-body dispersion interactions accounts for the electronic correlations that govern the adsorbate binding. We find the adsorbate properties to be strongly entropy driven, as can be judged by a kinetic molecular desorption prefactor of 1024 s-1 that largely exceeds previously reported estimates. We relate this effect to sizable fluctuations across structural and electronic observables. A comparison of our calculations to temperature-programed desorption measurements demonstrates that finite-temperature effects play a dominant role for flexible molecules in contact with polarizable surfaces, and that recently developed first-principles methods offer an optimal tool to reveal novel collective behavior in such complex systems.

  17. Structure and Hydrogen Bonding of Water in Polyacrylate Gels: Effects of Polymer Hydrophilicity and Water Concentration.

    Science.gov (United States)

    Mani, Sriramvignesh; Khabaz, Fardin; Godbole, Rutvik V; Hedden, Ronald C; Khare, Rajesh

    2015-12-10

    The ability to tune the hydrophilicity of polyacrylate copolymers by altering their composition makes these materials attractive candidates for membranes used to separate alcohol-water mixtures. The separation behavior of these polyacrylate membranes is governed by a complex interplay of factors such as water and alcohol concentrations, water structure in the membrane, polymer hydrophilicity, and temperature. We use molecular dynamics simulations to investigate the effect of polymer hydrophilicity and water concentration on the structure and dynamics of water molecules in the polymer matrix. Samples of poly(n-butyl acrylate) (PBA), poly(2-hydroxyethyl acrylate) (PHEA), and a 50/50 copolymer of BA and HEA were synthesized in laboratory, and their properties were measured. Model structures of these systems were validated by comparing the simulated values of their volumetric properties with the experimental values. Molecular simulations of polyacrylate gels swollen in water and ethanol mixtures showed that water exhibits very different affinities toward the different (carbonyl, alkoxy, and hydroxyl) functional groups of the polymers. Water molecules are well dispersed in the system at low concentrations and predominantly form hydrogen bonds with the polymer. However, water forms large clusters at high concentrations along with the predominant formation of water-water hydrogen bonds and the acceleration of hydrogen bond dynamics. PMID:26514915

  18. Uranium(VI) sequestration by polyacrylic and fulvic acids in aqueous solution

    International Nuclear Information System (INIS)

    Stability data on the formation of dioxouranium(VI) species with polyacrylic (PAA) and fulvic acids (FA) are reported with the aim to define quantitatively the sequestering capacity of these high molecular weight synthetic and naturally occurring ligands toward uranium(VI), in aqueous solution. Investigations were carried out at t = 25 deg C in NaCl medium at different ionic strengths and in absence of supporting electrolyte for uranyl-fulvate (UO22+-FA) and uranyl-polyacrylate (UO22+-PAA, PAA MW 2 kDa) systems respectively. The experimental data are consistent with the following speciation models for the two systems investigated: (i) UO2(FA1), UO2(FA1)(FA2), UO2(FA1)(FA2)(H) for UO22+-fulvate (where FA1 and FA2 represent the carboxylic and phenolic fractions, respectively, both present in the structure of FA), and (ii) UO2(PAA), UO2(PAA)(OH), (UO2)2(PAA)(OH)2 for UO22+-polyacrylate. By using the stability data obtained for all the complex species formed, the uranium(VI) sequestration by PAA and FA was expressed by the pL50 parameter [i.e. the -log(total ligand concentration) necessary to bind 50% of uranyl ion] at different pH values. A comparison between pL50 values of FA and PAA and some low molecular weight carboxylic ligands toward uranyl ion is also given. (author)

  19. Electrical conductivity and electromagnetic interference shielding characteristics of multiwalled carbon nanotube filled polyacrylate composite films

    International Nuclear Information System (INIS)

    Multiwalled carbon nanotubes (MWCNTs) were homogeneously dispersed in pure acrylic emulsion by ultrasonication to prepare MWCNT/polyacrylate composites applied on building interior wall for electromagnetic interference (EMI) shielding applications. The structure and surface morphology of the MWCNTs and MWCNT/polyacrylate composites were studied by field emission scanning microscopy (FESEM) and transmission electron microscopy (TEM). The electrical conductivity at room temperature and EMI shielding effectiveness (SE) of the composite films on concrete substrate with different MWCNT loadings were investigated and the measurement of EMI SE was carried out in two different frequency ranges of 100-1000 MHz (radio frequency range) and 8.2-12.4 GHz (X-band). The experimental results show that a low mass concentration of MWCNTs could achieve a high conductivity and the EMI SE of the MWCNT/polyacrylate composite films has a strong dependence on MWCNTs content in both two frequency ranges. The SE is higher in X-band than that in radio frequency range. For the composite films with 10 wt.% MWCNTs, the EMI SE of experiment agrees well with that of theoretical prediction in far field

  20. The capture and stabilization of curcumin using hydrophobically modified polyacrylate aggregates and hydrogels.

    Science.gov (United States)

    Harada, Takaaki; Pham, Duc-Truc; Lincoln, Stephen F; Kee, Tak W

    2014-08-01

    Hydrophobically modified polyacrylates are shown to suppress the degradation of the medicinal pigment curcumin under physiological conditions. In aqueous solution, the 3% octadecyl randomly substituted polyacrylate, PAAC18, forms micelle-like aggregates at a concentration of 1 wt %. Under both conditions, PAAC18 shows a remarkable ability to suppress the degradation of curcumin at pH 7.4 and 37 °C such that its degradation half-life is increased by 1600-2000-fold. The suppression of degradation is attributed to hydrophobic interactions between curcumin and the octadecyl substituents of PAAC18 within the micelle-like aggregates and the hydrogel, as indicated by 2D NOESY (1)H NMR spectroscopy. UV-visible absorption titration results are consistent with the interaction of curcumin with five octadecyl substituents on average, which appears to substantially exclude water and greatly decrease the curcumin degradation rate. Dynamic light scattering and zeta potential measurements show the average hydrodynamic diameters of the PAAC18 aggregates to be 0.86-1.15 μm with a negative surface charge. In contrast to the octadecyl substitution, the 3% dodecyl randomly substituted polyacrylate, PAAC12, shows a negligible effect on slowing the degradation of curcumin, consistent with the dodecyl substituents being insufficiently long to capture curcumin in a adequately hydrophobic environment. These observations indicate the potential for PAAC18 to act as a model drug delivery system. PMID:25029529

  1. Effect of Molecular Structure on the Performance of Polyacrylic Acid Superplasticizer

    Institute of Scientific and Technical Information of China (English)

    ZHANG Rongguo; GUO Huiling; LEI Jiaheng; ZHANG Anfu; GU Huajun

    2007-01-01

    The effects of structure parameters, such as molecular structure, segment kinds, molecular weight, and organic functional groups, on the performance of polyacrylic acid superplasticizer were discussed. According to the differences of chain sections, functional groups, etc, polyacrylic acid superplasticizer could be divided into A, B, C three parts. Among them, A chain section included sulfonic acid groups, B chain section carboxyl groups, C chain section polyester. Polyacrylic acid superplasticizers with different matching of A, B, C chain sections, different length of C chain section and different molecular weights were synthesized by acrylic acid, polyethylene glycol, sodium methyl allylsulfonate; the relation between the molecular structure and performance was also studied. The expetimental results indicate that the water-reduction ratio increases obviously with the increment of the proportion of sodium methyl allylsulfonate chain section in the molecular; the slump retention increases greatly with the increment of the proportion of acrylic acid chain section; the dispersion of cement particles increases with the increment of the chain length of polyethylene glycol; when the molecular weight is in the range of 5000, the dispersion and slump retentibity increase with the increment of the average molecular weight of polymers.

  2. Calorimetric and X-ray studies of clathrate hydrates of tetraisoamylammonium polyacrylates.

    Science.gov (United States)

    Terekhova, Irina S; Manakov, Andrey Yu; Soldatov, Dmitriy V; Suwinska, Kinga; Skiba, Sergey S; Stenin, Yuri G; Villevald, Galina V; Karpova, Tamara D; Yunoshev, Alexander S

    2009-04-30

    The structure of clathrate hydrates with tetraisoamylammonium polyacrylate salt incorporated as guest has been studied in this work. Also, quantitative studies on the stability changes of the clathrate hydrates with different degrees of cross-linking of the guest polymer (varied from 0 to 3%) have been conducted. A single crystal X-ray diffraction study of a crystal of the hydrate with linear (uncross-linked) tetraisoamylammonium polyacrylate as guest reveals a hexagonal structure (space group P6m2, a = 12.15 A, c =12.58 A at 100 K) with 39 host framework water molecules per one guest monomeric unit. Powder X-ray diffraction analyses confirm the identity of the above crystal structure of the hydrate with linear guest polymer and the crystal structure of the hydrates with cross-linked guest (hexagonal, a = 12.25 A, c =12.72 A at 276 K). In order to quantitatively determine the stability differences of the hydrates with the included guests having various degrees of cross-linking of the anionic chain, a series of differential scanning calorimetry measurements of the fusion enthalpy of the hydrate samples has been carried out. On the basis of the results obtained, a structural model describing the decrease in the stability of the clathrate hydrates with tetraisoamylammonium polyacrylate guest as a function of the degree of cross-linking of the guest polymer has been suggested. PMID:19344169

  3. Electrical conductivity and electromagnetic interference shielding characteristics of multiwalled carbon nanotube filled polyacrylate composite films

    Science.gov (United States)

    Li, Yong; Chen, Changxin; Zhang, Song; Ni, Yuwei; Huang, Jie

    2008-07-01

    Multiwalled carbon nanotubes (MWCNTs) were homogeneously dispersed in pure acrylic emulsion by ultrasonication to prepare MWCNT/polyacrylate composites applied on building interior wall for electromagnetic interference (EMI) shielding applications. The structure and surface morphology of the MWCNTs and MWCNT/polyacrylate composites were studied by field emission scanning microscopy (FESEM) and transmission electron microscopy (TEM). The electrical conductivity at room temperature and EMI shielding effectiveness (SE) of the composite films on concrete substrate with different MWCNT loadings were investigated and the measurement of EMI SE was carried out in two different frequency ranges of 100-1000 MHz (radio frequency range) and 8.2-12.4 GHz (X-band). The experimental results show that a low mass concentration of MWCNTs could achieve a high conductivity and the EMI SE of the MWCNT/polyacrylate composite films has a strong dependence on MWCNTs content in both two frequency ranges. The SE is higher in X-band than that in radio frequency range. For the composite films with 10 wt.% MWCNTs, the EMI SE of experiment agrees well with that of theoretical prediction in far field.

  4. Rheological characterization of cataplasm bases composed of cross-linked partially neutralized polyacrylate hydrogel.

    Science.gov (United States)

    Wang, Jian; Zhang, Hongqin; An, Dianyun; Yu, Jian; Li, Wei; Shen, Teng; Wang, Jianxin

    2014-10-01

    Viscoelasticity is a useful parameter for characterizing the intrinsic properties of the cross-linked polyacrylate hydrogel used in cataplasm bases. The aim of this study was to investigate the effects of various formulation parameters on the rheological characteristics of polyacrylate hydrogel. The hydrogel layers were formed using a partially neutralized polyacrylate (Viscomate(™)), which contained acrylic acid and sodium acrylate in different copolymerization ratios, as the cross-linked gel framework. Dihydroxyaluminum aminoacetate (DAAA), which produces aluminum ions, was used as the cross-linking agent. Rheological analyses were performed using a "stress amplitude sweep" and a "frequency sweep". The results showed that greater amounts of acrylic acid in the structure of Viscomate as well as higher concentrations of DAAA and Viscomate led to an increase in the elastic modulus (G'). However, greater amounts of acrylic acid in the structure of Viscomate and higher concentrations of DAAA had an opposite on the viscous modulus (G″); this might be owing to higher steric hindrance. The results of this study can serve as guidelines for the optimization of formulations for cataplasms. PMID:24865937

  5. Calculated photo-isomerization efficiencies of functionalized azobenzene derivatives in solar energy materials: azo-functional organic linkers for porous coordinated polymers

    International Nuclear Information System (INIS)

    Recently, we used a local orbital density functional theory code called FIREBALL, to study the photoisomerization process in azobenzene derivatives for solar energy materials. Azobenzene functional groups undergo photoisomerization upon light irradiation or application of heat. Zhou et al (2012 J. Am. Chem. Soc. 134 99–102) showed that these azobenzenes can then be introduced into metal–organic frameworks via an organic linker in order to create a reversible switch for CO2 adsorption. In this manuscript, we examined how the addition of organic linkers (isophthalic acid) changes the relaxation times, isomerization mechanism, and quantum yield for both the cis↔trans pathways. We then tuned these properties by substituting functional groups, finding an increase in quantum yield as well as improved optical properties. (paper)

  6. Photo-orientation of azobenzene side chain polymers parallel or perpendicular to the polarization of red HeNe light

    International Nuclear Information System (INIS)

    The mechanism of the light-induced orientation process of azobenzene-containing polymers caused by irradiation with linearly polarized red light is investigated. This process is surprising because there is almost no absorption at 633 nm. Depending on the photochemical pre-treatment and the exposure time, the azobenzene moieties can undergo two different orientation processes resulting in either a parallel or a perpendicular orientation with respect to the electric field vector of the incident light. The fast orientation of the photochromic groups with their long axis in the direction of the light polarization requires a photochemical pre-treatment in which non-polarized UV light generates Z-isomers. Due to this procedure the film becomes 'photochemically activated' for the subsequent polarized irradiation with red light. But on continued exposure a second, much slower reorientation process occurs which establishes an orientation of the azobenzene groups perpendicular to the electric field vector. The fast mechanism is probably caused by an angle-selective photo-isomerization of the Z-isomers to the E-isomers, while the subsequent slow reorientation process is caused by the well-known conventional photo-orientation taking place via the accumulation of a number of photoselection steps and the rotational diffusion minimizing the absorbance of the E-isomer. This process occurs in the steady state but at this wavelength with a very small concentration of Z-isomers. The competing mechanisms take place in the same polymer film under almost identical irradiation conditions, differing only in the actual concentration of the Z-isomers

  7. Base-Catalyzed Hydrophosphination of Azobenzenes with Diarylphosphine Oxides: A Precise Construction of N-N-P Unit.

    Science.gov (United States)

    Hong, Gang; Zhu, Xiaoyan; Hu, Chen; Aruma, Alfred Njasotapher; Wu, Shengying; Wang, Limin

    2016-08-01

    Addition of diarylphosphine oxides to the N═N double bond of azobenzenes leads to the formation of the P-substituted hydrazines in up to 98% yield for 24 examples, and the formation of diphenylphosphinic amides was observed in three substrates. This strategy features tolerance of a wide range of functional groups, simple operation, and mild reaction conditions. Specially, this method can be also applied to the gram-scale synthesis of the product. A polar reaction mechanism is also proposed based on control experiments. PMID:27387595

  8. Covalent functionalization of graphene by azobenzene with molecular hydrogen bonds for long-term solar thermal storage

    OpenAIRE

    Feng, Yiyu; Liu, Hongpo; Luo, Wen; Liu, Enzuo; Zhao, Naiqin; Yoshino, Katsumi; Feng, Wei

    2013-01-01

    Reduced graphene oxide-azobenzene (RGO-AZO) hybrids were prepared via covalent functionalization for long-term solar thermal storage. Thermal barrier (ΔEa ) of cis to tran reversion and thermal storage (ΔH) were improved by molecular hydrogen bonds (H-bonds) through ortho- or para-substitution of AZO. Intramolecular H-bonds thermally stabilized cis-ortho-AZO on RGO with a long-term half-life of 5400 h (ΔEa = 1.2 eV), which was much longer than that of RGO-para-AZO (116 h). RGO-para-AZO with o...

  9. Electrochemical lithiation performance and characterization of silicon-graphite composites with lithium, sodium, potassium, and ammonium polyacrylate binders.

    Science.gov (United States)

    Han, Zhen-Ji; Yamagiwa, Kiyofumi; Yabuuchi, Naoaki; Son, Jin-Young; Cui, Yi-Tao; Oji, Hiroshi; Kogure, Akinori; Harada, Takahiro; Ishikawa, Sumihisa; Aoki, Yasuhito; Komaba, Shinichi

    2015-02-01

    Poly(acrylic acid) (PAH), which is a water soluble polycarboxylic acid, is neutralized by adding different amounts of LiOH, NaOH, KOH, and ammonia (NH4OH) aqueous solutions to fix neutralization degrees. The differently neutralized polyacid, alkali and ammonium polyacrylates are examined as polymeric binders for the preparation of Si-graphite composite electrodes as negative electrodes for Li-ion batteries. The electrode performance of the Si-graphite composite depends on the alkali chemicals and neutralization degree. It is found that 80% NaOH-neutralized polyacrylate binder (a pH value of the resultant aqueous solution is ca. 6.7) is the most efficient binder to enhance the electrochemical lithiation and de-lithiation performance of the Si-graphite composite electrode compared to that of conventional PVdF and the other binders used in this study. The optimum polyacrylate binder highly improves the dispersion of active material in the composite electrode. The binder also provides the strong adhesion, suitable porosity, and hardness for the composite electrode with 10% (m/m) binder content, resulting in better electrochemical reversibility. From these results, the factors of alkali-neutralized polyacrylate binders affecting the electrode performance of Si-graphite composite electrodes are discussed. PMID:25559330

  10. Polyacrylate-water partitioning of biocidal compounds: enhancing the understanding of biocide partitioning between render and water.

    Science.gov (United States)

    Bollmann, Ulla E; Ou, Yi; Mayer, Philipp; Trapp, Stefan; Bester, Kai

    2015-01-01

    In recent years, the application of polymer-based renders and paints for façade coatings of buildings has risen enormously due to the increased mounting of thermal insulation systems. These materials are commonly equipped with biocides - algaecides, fungicides, and bactericides - to protect the materials from biological deterioration. However, the biocides need to be present in the water phase in order to be active and, hence, they are flushed of the material by rain water. In order to increase the knowledge about the partitioning of biocides from render into the water phase, partition constants between the polymer - in this case polyacrylate - and water were studied using glass fibre filters coated with polyacrylate. The polyacrylate-water partition constants (logKAcW) of ten biocides used in construction material varied between 1.66 (isoproturon) and 3.57 (dichloro-N-octylisothiazolinone). The correlation of the polyacrylate-water partition constants with the octanol-water partition constants is significant, but the polyacrylate-water partition constants were predominantly below octanol-water partition constants (Kow). The comparison with render-water distribution constants showed that estimating the leaching of biocides from render based on polymer-water partitioning is a useful and practical tool. PMID:25303663

  11. Azobenzene-aminoglycoside: Self-assembled smart amphiphilic nanostructures for drug delivery.

    Science.gov (United States)

    Deka, Smriti Rekha; Yadav, Santosh; Mahato, Manohar; Sharma, Ashwani Kumar

    2015-11-01

    Here, we have designed and synthesized a novel cationic amphiphilic stimuli-responsive azobenzene-aminoglycoside (a small molecule) conjugate, Azo-AG 5, and characterized it by UV and FTIR. Light responsive nature of Azo-AG 5 was assessed under UV-vis light. Self- assembly of Azo-AG 5 in aqueous solutions into nanostructures and their ability to act as drug carrier were also investigated. The nanostructures of Azo-AG 5 showed average hydrodynamic diameter of ∼ 255 nm with aminoglycoside moiety (neomycin) and 4-dimethylaminoazobenzene forming hydrophilic shell and hydrophobic core, respectively. In the hydrophobic core, eosin and aspirin were successfully encapsulated. Dynamic light scattering (DLS) measurements demonstrated that the nanoassemblies showed expansion and contraction on successive UV and visible light irradiations exhibiting reversible on-off switch for controlling the drug release behavior. Similar behavior was observed when these nanostructures were subjected to pH-change. In vitro drug release studies showed a difference in UV and visible light-mediated release pattern. It was observed that the release rate under UV irradiation was comparatively higher than that observed under visible light. Further, azoreductase-mediated cleavage of the azo moiety in Azo-AG 5 nanoassemblies resulted in the dismantling of the structures into aggregated microstructures. Azo-AG 5 nanostructures having positive surface charge (+9.74 mV) successfully interacted with pDNA and retarded its mobility on agarose gel. Stimuli responsiveness of nanostructures and their on-off switch like behavior ensure the great potential as controlled drug delivery systems and in other biomedical applications such as colon-specific delivery and gene delivery. PMID:26255160

  12. Biocides from façade coatings in urban surface waters: Estimating the leaching of biocides from render by polyacrylate-water partitioning constants?

    DEFF Research Database (Denmark)

    Bollmann, Ulla E.; Styszko, K.; Ou, Yi;

    2015-01-01

    polyacrylate-water partition constants in comparison to render-water distribution constants was introduced for this purpose. The results showed that polyacrylate-water partition constants might serve as a useful and practical tool which would be closer to the reality than the commonly used water solubilty and...

  13. Calculated photo-isomerization efficiencies of functionalized azobenzene derivatives in solar energy materials: azo-functional organic linkers for porous coordinated polymers

    Czech Academy of Sciences Publication Activity Database

    Neukirch, A.J.; Park, J.; Zobač, Vladimír; Wang, H.; Jelínek, Pavel; Prezhdo, O.V.; Zhou, H.-C.; Lewis, J.P.

    2015-01-01

    Roč. 27, č. 13 (2015), s. 134208. ISSN 0953-8984 R&D Projects: GA ČR(CZ) GA14-02079S Institutional support: RVO:68378271 Keywords : photoisomerization * azobenzene * metal - organic frameworks * molecular switches Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 2.346, year: 2014

  14. Cis-trans photoisomerization of azobenzene upon excitation to the S-1 state: An ab initio molecular dynamics and QM/MM study

    Czech Academy of Sciences Publication Activity Database

    Pederzoli, Marek; Pittner, Jiří; Barbatti, M.; Lischka, H.

    Bellingham: SPIE-INT SOC OPTICAL ENGINEERING, 2012 - (Dobisz, E.; Eldada, L.), s. 846318 ISBN 978-0-8194-9180-0. [Conference on Nanoengineering - Fabrication, Properties, Optics, and Devices /9./. San Diego (US), 14.08.2012-16.08.2012] Institutional support: RVO:61388955 Keywords : azobenzene * ab initio molecular dynamics * excited states Subject RIV: CF - Physical ; Theoretical Chemistry

  15. Holographic investigations of azobenzene-containing low-molecular-weight compounds in pure materials and binary blends with polystyrene.

    Science.gov (United States)

    Audorff, Hubert; Walker, Roland; Kador, Lothar; Schmidt, Hans-Werner

    2011-11-01

    This paper reports on the synthesis and the thermal and optical properties of photochromic low-molecular-weight compounds, especially with respect to the formation of holographic volume gratings in the pure materials and in binary blends with polystyrene. Its aim is to provide a basic understanding of the holographic response with regard to the molecular structure, and thus to show a way to obtain suitable rewritable materials with high sensitivity for holographic data storage. The photoactive low-molecular-weight compounds consist of a central core with three or four azobenzene-based arms attached through esterification. Four different cores were investigated that influence the glass transition temperature and the glass-forming properties. Additional structural variations were introduced by the polar terminal substituent at the azobenzene chromophore to fine-tune the optical properties and the holographic response. Films of the neat compounds were investigated in holographic experiments, especially with regard to the material sensitivity. In binary blends of the low-molecular-weight compounds with polystyrene, the influence of a polymer matrix on the behavior in holographic experiments was studied. The most promising material combination was also investigated at elevated temperatures, at which the holographic recording sensitivity is even higher. PMID:21956207

  16. Poly(acrylic acid) to induce competitive crystallization of a theophylline/oxalic acid cocrystal and a theophylline polymorph

    Science.gov (United States)

    Jang, Jisun; Kim, Il Won

    2016-01-01

    Polymeric additives to induce competitive crystallization of pharmaceutical compounds were explored. A cocrystal of theophylline and oxalic acid was used as a model system, and poly(acrylic acid), poly(caprolactone), and poly(ethylene glycol) were the additives. The cocrystal formation was selectively hindered with addition of poly(acrylic acid). First the size of the cocrystals were reduced, and eventually the cocrystallization was inhibited to generate neat theophylline crystals. The theophylline crystals were of a distinctively different crystal structure from known polymorphs, based on powder X-ray diffraction. They were also obtained in nanoscale size, when millimeter-scale crystals formed without poly(acrylic acid). Polymeric additives that could form specific interactions with crystallizing compounds seem to be useful tools for the phase and size control of pharmaceutical crystals.

  17. Antibacterial activity of chitosan and the interpolyelectrolyte complexes of poly(acrylic acid-chitosan

    Directory of Open Access Journals (Sweden)

    Hortensia Ortega-Ortiz

    2010-06-01

    Full Text Available The antimicrobial activity of chitosan and water soluble interpolyelectrolyte complexes of poly(acrylic acid-chitosan was studied. Chitosans of two different molecular weights were tested at different concentration for 0.5 to 5 g·L-1 as antimicrobial agents against P. aeruginosa and P. oleovorans. In both cases, the best microbial inhibition was obtained with the concentration of 5 g·L-1. However, the interpolyelectrolyte complexes of poly(acrylic acid-chitosan with composition φ =2 produced higher antibacterial activity than the two chitosans at the concentration of 0.5 g·L-1. The NPEC2 complex was more effective than chitosans. This could be attributed to the number of moles of the amino groups of chitosan and the carboxylic acid groups of the interpolyelectrolyte complexes poly(acrylic acid.A atividade antimicrobiana de quitosana e complexos interpolieletrolíticos hidrossoluvéis de poli(ácido acrílico-quitosana foi estudada. Quitosanas de dois diferentes pesos moleculares foram testados em diferentes concentrações, 0,5 a 5 g • L-1, como agentes antimicrobianos nas P. aeruginosa e P. oleovorans. Em ambos os casos, obteu-se a melhor inibição microbiana com a concentração de 5 g • L-1, no entanto os complexos interpolieletrolíticos de poli (ácido acrílico-quitosana com composição φ = 2 apresentaram maior atividade antibacteriana do que os dois quitosans na concentração de 0,5 g • L-1. O complexo NPEC2 foi mais eficaz do que as quitosanas, sendo que o resultado pode ser atribuído ao número de moles dos grupos aminos da quitosana e aos grupos carboxílicos dos complexos de poli(ácido acrílico.

  18. Studies of radiolytic and self-radiolytic processes in polyacrylic hydrogels using ESR spectrometry

    International Nuclear Information System (INIS)

    Due to its remarkable capacity of water retaining capacity, polyacrylic (PAA) hydrogels represent an interesting alternative for tritium (tritiated water-HTO) liquid waste trapping. The study was focused on radiolytic processes in PAA:HTO systems derived from irradiation of polymeric network by decay of tritium atoms from HTO. The aim of these studies is to identify the polymeric structures and the optimal storage conditions. ESR studies of radiolytic processes were performed on dry polyacrylic acid (PAA) and polyacrylic based hydrogels samples irradiated at 77 K. In this study we observed the effect of swelling capacity of hydrogel on the formation of free radicals. In the ESR spectra of irradiated PAA a signal with quintet structure was identified and assigned in accordance with the literature, to a radical in α position with respect to the carboxylic group. We also identified a triplet that was ascribed to a radical resulting from fragmentation of polymeric main chain. In case of PAA hydrogels signals were identified and ascribed to the HO radical resulted from water radiolysis, R-OO radicals resulted from the presence of atmospheric O2 in samples as well a signal with quintet structure less split than in the dry polymer. This signal was ascribed to a radical bound to the polymeric main chain in α position relative to carboxylic group. The decrease of split parameter is determined by tension of the main chain as a result of swelling, associated with increase of θ angle between px axis of Cα radical and the Cα Cβ and Hβ plane. The ESR analysis of labelled hydrogels reveals the presence of HO and COO radicals produced by internal primary effect. ESR analysis of PAA:HTO samples indicate the preponderant role of the internal primary effect in selfradiolytic effects in concordance with the role of secondary effects which are blocked in the ESR study due to material freezing. (authors)

  19. Studies of radiolytic and self-radiolytic processes in polyacrylic hydrogels using RES spectrometry

    International Nuclear Information System (INIS)

    Due to the remarkable capacity of retaining water, the polyacrylic (PAA) hydrogels represent an interesting alternative for tritium (tritiated water-HTO) liquid wastes trapping. The study was addressed to radiolytic processes in PAA:HTO systems derived from irradiation of polymeric network by decay of tritium from HTO. The aim of these studies is the identification of polymeric structures and optimal storage conditions. ESR studies of radiolytic processes were carried out on dry polyacrylic acid (PAA) and polyacrylic based hydrogels irradiated and determined at 77 K. In the study we observed the effect of swelling capacity of hydrogel in forming free radicals. In ESR spectra of irradiated PAA a signal with quintet structure was identified and assigned, according to the literature, to radical from a position referred to carboxylic group. We also identified a triplet assigned to a radical resulting from the fragmentation of polymeric main chain. In case of PAA hydrogels signals assigned to HO· radical resulting from water radiolysis were identified, to R-OO· radicals, resulting from the presence of atmospheric O2 in samples as well as a signal with quintet structure more less split like dry polymer. The signal is assigned to a radical from the polymeric main chain in a position referred to carboxylic group. The decrease of split parameter is determined by tension of main chain as result of swelling, associated with increase of θ angle between px axis of Cα radical and the Cα Cβ Hβ plane. ESR analysis of labelled hydrogels indicates the presence of HO and COO radicals resulting from internal primary effect. ESR analysis of PAA:HTO samples indicate the dominant role of the internal primary effect in selfradiolytical effects according with the role of secondary effects stopped in ESR study due to freezing material. (authors)

  20. Studies of radiolytic and self-radiolytic processes in polyacrylic hydrogels using ESR spectrometry

    International Nuclear Information System (INIS)

    Full text: Due to the remarkable capacity of water retaining, polyacrylic (PAA) hydrogels represent an interesting alternative for tritium (tritiated water-HTO) liquid wastes trapping. The study was developed on radiolytic processes in PAA:HTO systems derived from irradiation of polymeric network by decay of tritium atoms from HTO. The aim of these studies is the identification of polymeric structures and optimal storage conditions. ESR studies of radiolytic processes were carried out on dry polyacrylic acid (PAA) and polyacrylic based hydrogels irradiated and determined at 77 K. In the study we observed the effect of swelling capacity of hydrogel on the formation of free radicals. In the ESR spectra of irradiated PAA was identified a signal with quintet structure assigned, according to the literature, to radical from a position referred to the carboxylic group. We also identified a triplet assigned to a radical resulted by fragmentation of polymeric main chain. In the case of PAA hydrogels signals were identified and attributed to HO radical resulted from water radiolysis, R-OO radicals resulted from the presence of atmospheric O2 in samples and a signal with quintet structure more less split like dry polymer. The signal is attributed to a radical from the polymeric main chain in α position referred to carboxylic group. The decrease of split parameter is determined by tension of main chain as result of swelling, associated with increase of θ angle between px axis of Cα radical and the Cα Cβ Hβ plane. ESR analysis of labelled hydrogels indicates the presence of HO and COO radicals resulted from internal primary effect. ESR analysis of PAA:HTO samples indicates the preponderant role of the internal primary effect in self radiolytic effects in concordance with the role of secondary effects stopped in ESR study due to freeze material. (author)

  1. Thiomers: Influence of molecular mass and thiol group content of poly(acrylic acid) on efflux pump inhibition.

    Science.gov (United States)

    Grabovac, Vjera; Laffleur, Flavia; Bernkop-Schnürch, Andreas

    2015-09-30

    The aim of the present study was to investigate the influence of molecular mass and thiol group content of poly(acrylic acid)-cysteine conjugates on the permeation of sulforhodamine 101 and penicillin G. acting as substrates for multidrug resistance-associated protein 2 efflux pump. Poly(acrylic acids) of 2 kDa, 100 kDa, 250 kDa, 450 kDa and 3000 kDa were conjugated with cysteine. The thiol group content of all these polymers was in the range from 343.3 ± 48.4 μmol/g to 450.3 ± 76.1 μmol/g. Transport studies were performed on rat small intestine mounted in Ussing-type chambers. Since 250 kDa poly(acrylic acid) showed the highest permeation enhancing effect, additionally thiolated 250 kDa polyacrylates displaying 157.2 μmol/g, 223.0 ± 18.1 and 355.9 μmol/g thiol groups were synthesized in order to investigate the influence of thiol group content on the permeation enhancement. The permeation of sulforhodamine was 3.93- and 3.85-fold improved using 250 kDa poly(acrylic acid)-cysteine conjugate exhibiting 355.9 ± 39.5 μmol/g and 223.0 ± 18.1 μmol/g thiol groups. Using the same conjugates the permeation of penicillin G was 1.70- and 1.59-fold improved, respectively. The study demonstrates that thiolated poly(acrylic acid) inhibits Mrp2 mediated transport and that the extent of inhibition depends on the molecular mass and degree of thiolation of the polymer. PMID:26238816

  2. Measurement of respirable superabsorbent polyacrylate (SAP) dust by ethanol derivatization using gas chromatography-mass spectrometry (GC-MS) detection.

    Science.gov (United States)

    McCormack, Paul; Lemmo, John S; Macomber, Margaret; Holcomb, Mark L; Lieckfield, Robert

    2011-04-01

    Superabsorbent polyacrylate (SAP) is an important industrial chemical manufactured primarily as sodium polyacrylate but occasionally as potassium salt. It has many applications owing to its intrinsic physical property of very high water absorption, which can be more than 100 times it own weight. SAP is commonly used in disposable diapers and feminine hygiene products and is known by a number of synonyms-sodium polyacrylate, superabsorbent polyacrylate (SAP), polyacrylate absorbent (PA), and superabsorbent material (SAM). Germany and The Netherlands have adopted a nonbinding scientific guideline value 0.05 mg/m³ (8-hr time-weighted average, TWA) as the maximum allowable workplace concentration for the respirable dust of SAP (polyacrylate dust collected on filter cassettes in the workplace environment. This method is an alternative to the commonly used sodium-based method, which is limited owing to potential interference by other sources of sodium from the workplace and laboratory environments. The alcohol derivatization method effectively eliminates sodium interference from several classes of sodium compounds, as shown by their purposeful introduction at two and six times the equivalent amount of SAP present in reference samples. The accuracy of the method, as determined by comparison with sodium analysis of known reference samples, was greater than 80% over the study range of 5-50 μg of SAP dust. The lower reporting limit of the method is 3.0 μg of SAP per sample, which is equivalent to 3 (μg/m³) for an 8-hr sampling period at the recommended flow rate of 2.2 L/min. PMID:21416441

  3. Kinetics and mechanism of photocatalytic aging of polyacrylic acid and polyacrylamide at 770K

    International Nuclear Information System (INIS)

    This work is aimed at elucidating the mechanism of photoradical aging of polyacrylic acid and polyacrylamide, at obtaining quantitative properties of the intermediate stages of this process, and at establishing a relationship between photochemical reactions of macroradicals and changes in molecular weight of the polymers. Radicals were generated by irradiation with a cobalt 60 source at 77 K. High-pressure mercury lamps were used as the light source. Molecular weights were determined by ebulliography and photometry. The accumulation of carbon monoxide and ketenes was monitored as a function of reaction time. ESR spectra and hyperfine structure were also assessed in determining the reaction pathways

  4. Acidic polyanion poly(acrylic acid) prevents calcium oxalate crystal deposition

    OpenAIRE

    Kleinman, Jack G.; Alatalo, Laura J.; Beshensky, Ann M.; Wesson, Jeffrey A.

    2008-01-01

    Acidic macromolecules inhibit calcium oxalate nucleation, growth, aggregation and attachment to cells in vitro. To test for such an effect in vivo we used osmotic minipumps to continuously infuse several doses of the 5.1 kDa poly(acrylic acid) (pAA5.1) into rats fed a diet which causes renal calcium oxalate crystal deposition. Although kidneys of rats receiving the saline control contained calcium oxalate crystals, measured by polarized light microscopy, those of animals given pAA5.1 had sign...

  5. Dynamic Behavior and Mass Transport in Polyacrylic Acid Gel by Dynamic Light Scattering

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Dynamic behaviors on polyacrylic acid (PAA) gels and mass (small molecules) transports in the gels have been studied mainly by dynamic light scattering (DLS). The cross-linking degree (fc), monomer concentration (Cm) and temperature of the gels have significant influences on its dynamic behavior and mass transport in the gels. The increase of fc leads to decrease of the mesh sizes of the gels, thus the obstacle of the gels for mass transport is increased. As a result, small molecular diffusion Dk in the gels is decreased. So even if for small molecules, the Dk also is influenced.

  6. FTIR-ATR monitoring and SEC/RI/MALLS characterization of ATRP synthesized hyperbranched polyacrylates

    OpenAIRE

    Gonçalves, Miguel; Pinto, Virgínia; Dias, Rolando; Costa, Mário Rui

    2010-01-01

    This work reports the synthesis at 1 L scale of hyperbranched polyacrylates based upon acrylate/diacrylate monomers such as n-butyl acrylate (nBA)/1,6-hexanediol diacrylate (HDDA) and using atom transfer radical polymerization (ATRP). A FTIR-ATR immersion probe was used to monitor the polymerization reaction. The dynamics of the build-up of polymer structure was studied by off-line analysis of samples at different reaction times by size exclusion chromatography (SEC) with detection of refract...

  7. Star-Shaped Polyacrylates: Highly Functionalized Architectures via CuAAC Click Conjugation.

    Science.gov (United States)

    Lammens, Mieke; Fournier, David; Fijten, Martin W M; Hoogenboom, Richard; Prez, Filip Du

    2009-12-01

    Well-defined functional star-shaped polymer structures with up to 29 arms have been successfully synthesized by the combination of atom transfer radical polymerization (ATRP) and click chemistry. First, azide end-functionalized poly(isobornyl acrylate) (PiBA) star-shaped polymers were prepared by successive ATRP and bromine substitution. Subsequently, alkyne end-functionalized molecules and polymers were introduced onto the star-shaped PiBA bearing pendant azide moieties by copper-catalyzed azide-alkyne cycloaddition (CuAAC). The possibilities and limits for the CuAAC on such highly branched polyacrylates are described. PMID:21638494

  8. Preparation of carboxymethyl chitosan grafted polyacrylic acid hydrogel and its evaluation in vitro and in vivo

    OpenAIRE

    Yuqin CUI; Yingge ZHAO; Ruiqiong TIAN; Zhang, Xiaoyun; Qing SHANG

    2015-01-01

    A novel pH-sensitive carboxymethyl chitosan graft polyacrylic acid(CMC-g-PAA) hydrogel is fabricated via a free radical heat-initiated graft copolymerization reaction with acrylic acid(AA) and carboxymethyl chitosan(CMC) as monomers. The polymerization is successful, which is confirmed via fourier transform infrared spectroscopy (FT-IR). The result of swelling experiment indicates that the final CMC-g-PAA hydrogel has significant pH-sensitivity. Insulin(INS), as a model drug, is loaded into t...

  9. Ultra-Thin Films of Poly(acrylic acid)/Silver Nanocomposite Coatings for Antimicrobial Applications

    OpenAIRE

    Alaa Fahmy; Eisa, Wael H.; Mohamed Yosef; Ali Hassan

    2016-01-01

    In this work not only colloids of poly(acrylic acid) (PAA) embedded with silver nanoparticles (Ag-NPs) but thin films (10 nm) also were deposited using electrospray deposition technique (ESD). A mixture of sodium borohydride (NaBH4) and ascorbic acid (AA) were utilized to reduce the silver ions to generate Ag-NPs in the PAA matrix. Moreover, sodium tricitrate was used to stabilize the prepared colloids. The obtained colloids and films were characterized using UV-visible, transmission electron...

  10. New composite systems on the base of polyethylene porous films covered by polypyrrole and polyacrylic acid

    Czech Academy of Sciences Publication Activity Database

    Elyashevich, G. K.; Rosova, E. Yu.; Andreeva, D. V.; Polotskaya, G. A.; Trchová, Miroslava; Pientka, Zbyněk

    2005-01-01

    Roč. 97, č. 4 (2005), s. 1410-1417. ISSN 0021-8995 R&D Projects: GA ČR GA202/02/0698 Grant ostatní: Russian Foundation of Basic Research(RU) 01-03-32290; Russian Foundation of Basic Research(RU) 04-03-32229 Institutional research plan: CEZ:AV0Z40500505 Keywords : porous polyethylene films * polypyrrole * polyacrylic acid Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.072, year: 2005

  11. Adsorption of sodium polyacrylate in high solids loading calcium carbonate slurries.

    Science.gov (United States)

    Taylor, Joshua J; Sigmund, Wolfgang M

    2010-01-15

    The adsorption of sodium polyacrylate (NaPAA) in slurries with up to 75 wt.% calcium carbonate was investigated with the use of attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) and adsorption of probe molecules. Analysis of the IR spectra demonstrated that the carboxylate groups of NaPAA adsorbed onto ground calcium carbonate (GCC) in three different modes. These modes were shown to be dependent on the solids loading and age of the slurry. Further investigation lead to the determination of the chelating ability of NaPAA at high solids loading. PMID:19875128

  12. Experimental evidence for two thermodynamic length scales in neutralized polyacrylate gels

    Science.gov (United States)

    Horkay, Ferenc; Hecht, Anne-Marie; Grillo, Isabelle; Basser, Peter J.; Geissler, Erik

    2002-11-01

    The small angle neutron scattering (SANS) behavior of fully neutralized sodium polyacrylate gels is investigated in the presence of calcium ions. Analysis of the SANS response reveals the existence of three characteristic length scales, two of which are of thermodynamic origin, while the third length is associated with the frozen-in structural inhomogeneities. This latter contribution exhibits power law behavior with a slope of about -3.6, reflecting the presence of interfaces. The osmotically active component of the scattering signal is defined by two characteristic length scales, a correlation length ξ and a persistence length L.

  13. Structure and Proton Conductivity in Mixtures of Poly(acrylic acid) and Imidazole

    Science.gov (United States)

    Yang, Han-Chang; Griffin, Philip J.; Winey, Karen I.; University of Pennsylvania Team

    2015-03-01

    Proton conductivity in polymer electrolyte membranes (PEMs) typically involves water, which requires that during operation the humidity of the PEM be carefully controlled. In contrast, anhydrous protic polymer membranes promote proton transport by incorporating heterocyclic molecules, such as imidazole and its derivatives, into acid-containing polymers. In this work, we explore the interplay between nanoscale-structure and proton conduction of poly(acrylic acid) (PAA) blended at varying compositions with 2-ethyl-4-methylimidazole (EMI). We present the glass transition temperature from differential scanning calorimetry, morphology characterization from X-ray scattering, and proton conductivity from electrical impedance spectroscopy.

  14. Bioinspired bioadhesive polymers: dopa-modified poly(acrylic acid) derivatives.

    Science.gov (United States)

    Laulicht, Bryan; Mancini, Alexis; Geman, Nathanael; Cho, Daniel; Estrellas, Kenneth; Furtado, Stacia; Hopson, Russell; Tripathi, Anubhav; Mathiowitz, Edith

    2012-11-01

    The one-step synthesis and characterization of novel bioinspired bioadhesive polymers that contain Dopa, implicated in the extremely adhesive byssal fibers of certain gastropods, is reported. The novel polymers consist of combinations of either of two polyanhydride backbones and one of three amino acids, phenylalanine, tyrosine, or Dopa, grafted as side chains. Dopa-grafted hydrophobic backbone polymers exhibit as much as 2.5 × the fracture strength and 2.8 × the tensile work of bioadhesion of a commercially available poly(acrylic acid) derivative as tested on live, excised, rat intestinal tissue. PMID:23008096

  15. Effects of Polar Organic Solvent on Separation of Y(edta)-/Nd(edta)- Complexes on Polyacrylic Anion Exchangers

    Institute of Scientific and Technical Information of China (English)

    Halina Hubicka; Dorota Kolodynska

    2005-01-01

    The use of polar organic solvents for the separations of rare earth elements (Ⅲ) is effective especially for their extensive separations despite the solubility limitations. The study shows that polyacrylate anion exchangers, particularly the weakly basic, gel anion exchanger Amberlite IRA 68, can be applied to the separation of rare earth complexes with EDTA in H2O-methanol and H2O-ethanol systems. In most cases the determined distribution coefficients of Ln3+ complexes with EDTA in mixed media like water-methanol on polyacrylate anion exchangers are larger than those in pure water media.

  16. Complexation of polyacrylates by Ca2+ ions. Time-resolved studies using attenuated total reflectance Fourier transform infrared dialysis spectroscopy.

    Science.gov (United States)

    Fantinel, Fabiana; Rieger, Jens; Molnar, Ferenc; Hübler, Patrick

    2004-03-30

    The attenuated total reflectance Fourier transform infrared dialysis technique is introduced for the time-resolved investigation of the binding processes of Ca2+ to polyacrylates dissolved in water. We observed transient formation of intermediates in water with various types of coordination of the carboxylate group to Ca2+ throughout the complexation steps. Time-resolved changes in the spectra were analyzed with principal component analysis, from which the spectral species were obtained as well as their formation kinetics. We propose a model for the mechanisms of Ca2+ coordination to polyacrylates. The polymer chain length plays an important role in Ca2+ binding. PMID:15835120

  17. The pH-responsive behaviour of poly(acrylic acid) in aqueous solution is dependent on molar mass.

    OpenAIRE

    Swift, T; Swanson, L.; Geoghegan, M; Rimmer, S.

    2016-01-01

    Fluorescence spectroscopy on a series of aqueous solutions of poly(acrylic acid) containing a luminescent label showed that polymers with molar mass, Mn < 16.5 kDa did not exhibit a pH responsive conformational change, which is typical of higher molar mass poly(acrylic acid). Below this molar mass, polymers remained in an extended conformation, regardless of pH. Above this molar mass, a pH-dependent conformational change was observed. Diffusion-ordered nuclear magnetic resonance spectroscopy ...

  18. The Study of Water Stability for SBS and Polyacrylate Composite Modified Asphalt Mixture

    Directory of Open Access Journals (Sweden)

    HU Qiusheng

    2014-09-01

    Full Text Available Polyacrylate (Polyacrylate, called PAE is a kind of thermoplastic polymer latex, which is easy to form a waterproof membrane and has greater adhesion ,always be used in concrete to enhance its ability to resist water corrosion.SBS is an inorganic modifier for modified asphalt mixture will help to improve the high and low temperature stability and other road performance, ect.However,its ability to enhanced asphalt mixture’s resistance for water damage is not obvious. In order to research the two composite modified asphalt mixture’s resistance effects to water damage , the Marshall Stability Test and Fort Kentucky Flooding Scattering Experiments were used on asphalt mixtures, SBS modified asphalt mixture and composite modified asphalt mixture and the effect of different composite modified PAE content were studied. The results showed that: PAE can significantly improve the water stability of asphalt mixture, what’s more, with the increase use of PAE,the mass loss rate of asphalt mixture decreases steadily.

  19. Thermodynamic Equilibrium Morphology Prediction of Polyurethane/Polyacrylate Composite Latex Particles

    Institute of Scientific and Technical Information of China (English)

    CHAI Shu-Ling; JIN Ming-Martin

    2008-01-01

    Composite particles were prepared by seeded surfactant-free batch emulsion polymerization at 80 ℃ using K2S2O8 as an initiator, and polyurethane aqueous dispersion as seed particles. The acrylate monomers were continuously added into the reactor under a starving condition in the second stage polymerization. The synthesized hybrid emulsions were found to form an inverted core-shell structure with polyacrylate as the core and with polyurethane as the shell from the observation with a transmission electron microscope. The interfacial tensions between polymer and polymer as well as polymer and water were calculated with a simple method according to harmonic mean equation and used in a mathematical model based on the minimum interfacial energy change principle to predict the equilibrium morphology. The observed particle morphologies were in good agreement with the predicted ones. The surface properties of the dried films formed from polyurethane (PU)/polyacrylate (PA) composite emulsions were also studied by contact angle measurements, showing that the shell part of the composite emulsions is preferentially oriented toward the surface layers of the dried films.

  20. Reinforced polyacrylates by UV and EB curing: preparation, structure and possible applications

    International Nuclear Information System (INIS)

    Reinforced polyacrylates were obtained by UV and electron beam (EB) curing using nano-sized silica particles as fillers for acrylates. The surface of the silica was chemically modified to improve embedding of the filler within the acrylate matrix. The modification was done using methacryloxypropyl trimethoxysilane and as product of an acid catalysed condensation of the organosilanes a polysiloxane shell is formed. This shell is linked to the silica via reaction with the surface silanol groups of the silica. The appearance of covalent Si-O-Si-R bonds formed either by the condensation of silanes and / or by the reaction with Si-OH groups on the silica was demonstrated by multinuclear MAS NMR and mass spectroscopy. Typically, an acrylate-nanocomposite formulation contains up to 35 wt.-% of polysiloxane covered nano-sized silica. The polysiloxane shell still carries methacrylate groups, these can copolymerize with acrylates and after UV or EB curing of such a formulation polyacrylate nanocomposites are obtained. These composite materials exhibit markedly improved properties as compared to pure polymers, e.g. an increased modulus and heat resistance, improved scratch and abrasion resistance as well as reduced gas permeabilities. This makes them very promising as coatings for technical applications. (Author)

  1. Investigation of small molecular weight poly(acrylic acid) adsorption on γ-alumina

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Lei; Luo, Shi-Zhong [College of Chemical Engineering, Sichuan University, Chengdu, Sichuan 610065 (China); Wang, Bin, E-mail: bin_wang@scu.edu.cn [College of Chemical Engineering, Sichuan University, Chengdu, Sichuan 610065 (China); Guo, ZhanHu [Chemical and Biomolecular Engineering Department, University of Tennessee, Knoxville, TN 37996 (United States)

    2015-08-01

    Highlights: • Small molecular weight poly(acrylic acid) incorporated on γ-alumina. • PAA adsorbed primarily on outer surface of alumina at low pH. • PAA infiltrated inside alumina pore at high pH. • Polymer chain reptation motion during the infiltration. - Abstract: The interactions between poly(acrylic acid) (PAA) and alumina have been widely investigated. In this study, the pattern of small molecular weight PAA (M{sub W} 3000) interaction with γ-alumina has been dissected. The alumina/PAA hybrids were prepared at pH 4.0, 5.5, and 7.0, respectively. Nitrogen absorption–desorption analysis, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, and elemental analysis were conducted to illustrate the characteristics of the hybrids. At pH 4.0, the coiled PAA conformation yielded polymer adsorption primarily on alumina outer surface. At higher pH values, the more stretched PAA molecules were able to infiltrate inside the alumina pores. The phenomenon is explained by the polymer chain reptation motion model. Coiled polymer chains are not oriented enough to penetrate the oxide pore channels. In contrary, stretched polymer chains are more likely to move along the pore channels.

  2. Research on various factors influencing the moisture absorption property of sodium polyacrylate

    Institute of Scientific and Technical Information of China (English)

    ZHANG ChunXiao; ZHANG WanXi; PAN ZhenYuan; ZHANG XiYao; LIU Jian; YUE ChongWang

    2009-01-01

    Sodium polyacrylate was synthesized with acrylic acid as the monomer,and sodium bisulfate and ammonium persulfate as the initiator,by means of aqueous solution polymerization.The factors influencing the properties of moisture absorption,such as monomer concentration,dosage of initiator,and reaction temperature were systematically investigated.The experimental results indicate that the moisture-absorbing property of this polymer was better than other traditional material,such as silica gel,and molecular sieve.The best reaction condition and formula are based on the orthogonal experiment design.The optimum moisture absorbency of sodium polyacrylate reaches 1.01 g/g.The mathematical correlation of this polymer with various factors and moisture absorbency is obtained based on the multiple regression analysis.The moisture content intuitive analysis table shows that neutralization degree has the most significant influence on moisture absorbency,followed by monomer concentration and reaction temperature,while other factors have less influence.

  3. Investigation of small molecular weight poly(acrylic acid) adsorption on γ-alumina

    International Nuclear Information System (INIS)

    Highlights: • Small molecular weight poly(acrylic acid) incorporated on γ-alumina. • PAA adsorbed primarily on outer surface of alumina at low pH. • PAA infiltrated inside alumina pore at high pH. • Polymer chain reptation motion during the infiltration. - Abstract: The interactions between poly(acrylic acid) (PAA) and alumina have been widely investigated. In this study, the pattern of small molecular weight PAA (MW 3000) interaction with γ-alumina has been dissected. The alumina/PAA hybrids were prepared at pH 4.0, 5.5, and 7.0, respectively. Nitrogen absorption–desorption analysis, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, and elemental analysis were conducted to illustrate the characteristics of the hybrids. At pH 4.0, the coiled PAA conformation yielded polymer adsorption primarily on alumina outer surface. At higher pH values, the more stretched PAA molecules were able to infiltrate inside the alumina pores. The phenomenon is explained by the polymer chain reptation motion model. Coiled polymer chains are not oriented enough to penetrate the oxide pore channels. In contrary, stretched polymer chains are more likely to move along the pore channels

  4. A convenient method to prepare emulsified polyacrylate nanoparticles from powders [corrected] for drug delivery applications.

    Science.gov (United States)

    Garay-Jimenez, Julio C; Turos, Edward

    2011-08-01

    We describe a method to obtain purified, polyacrylate nanoparticles in a homogeneous powdered form that can be readily reconstituted in aqueous media for in vivo applications. Polyacrylate-based nanoparticles can be easily prepared by emulsion polymerization using a 7:3 mixture of butyl acrylate and styrene in water containing sodium dodecyl sulfate as a surfactant and potassium persulfate as a water-soluble radical initiator. The resulting emulsions contain nanoparticles measuring 40-50 nm in diameter with uniform morphology, and can be purified by centrifugation and dialysis to remove larger coagulants as well as residual surfactant and monomers associated with toxicity. These purified emulsions can be lyophilized in the presence of maltose (a non-toxic cryoprotectant) to provide a homogeneous dried powder, which can be reconstituted as an emulsion by addition of an aqueous diluent. Dynamic light scattering and microbiological experiments were carried out on the reconstituted nanoparticles. This procedure allows for ready preparation of nanoparticle emulsions for drug delivery applications. PMID:21704525

  5. Clay-polymer nanocomposite material from the delamination of kaolinite in the presence of sodium polyacrylate.

    Science.gov (United States)

    Letaief, Sadok; Detellier, Christian

    2009-09-15

    A chemical route for the delamination of kaolinite in a polymeric matrix is reported in this work. The strategy that was used is based on mixing polyelectrolytes of opposite charges, an organic polyanion, polyacrylate, with an inorganic polycation resulting from the modification of the internal surfaces of kaolinite. The delamination was carried out by the reaction of sodium polyacrylate (PANa) with kaolinite whose internal aluminol surfaces were previously grafted with triethanolamine and subsequently quaternized with iodomethane (TOIM-K) to form an extended lamellar inorganic polycation. X-ray diffraction as well as scanning electron microscopy (SEM) confirmed the complete delamination of the kaolinite particles. 13C CP/MAS NMR showed the removal of the ammonium groups resulting from hydrolysis of the internal surfaces once exposed, and 29Si CP/MAS NMR spectra were in agreement with the retention of the 1:1 aluminosilicate kaolinite layers structures. From the thermogravimetry (TG) data, the respective percentages in mass of PA and kaolinite in the delaminated nanocomposite could be estimated to be 61% and 39%, respectively, in the conditions of the particular experiment. The procedure was repeated several times to show the reproducibility of the delamination. The interlayer functionalization of kaolinite was crucial for the success of the delamination procedure. SEM pictures show that some individual kaolinite platelets fold and form curved structures. PMID:19518083

  6. A facile one pot strategy for the synthesis of well-defined polyacrylates from acrylic acid via RAFT polymerization.

    Science.gov (United States)

    Li, Qianbiao; Wang, Taisheng; Dai, Jingwen; Ma, Chao; Jin, Bangkun; Bai, Ruke

    2014-03-28

    A facile one pot strategy for the preparation of linear and hyperbranched polyacrylates has been successfully developed by the combination of in situ esterification of acrylic acid with halogenated compounds promoted by 1,1,3,3-tetramethylguanidine (TMG) and RAFT polymerization. PMID:24534953

  7. Sustainable and scalable production of monodisperse and highly uniform colloidal carbonaceous spheres using sodium polyacrylate as the dispersant.

    Science.gov (United States)

    Gong, Yutong; Xie, Lei; Li, Haoran; Wang, Yong

    2014-10-28

    Monodisperse, uniform colloidal carbonaceous spheres were fabricated by the hydrothermal treatment of glucose with the help of a tiny amount of sodium polyacrylate (PAANa). This synthetic strategy is effective at high glucose concentration and for scale-up experiments. The sphere size can be easily tuned by the reaction time, temperature and glucose concentration. PMID:25199065

  8. Comparison of various models to describe the charge-pH dependence of poly(acrylic acid)

    NARCIS (Netherlands)

    Lützenkirchen, J.; Male, van J.; Leermakers, F.A.M.; Sjöberg, S.

    2011-01-01

    The charge of poly(acrylic acid) (PAA) in dilute aqueous solutions depends on pH and ionic strength. We report new experimental data and test various models to describe the deprotonation of PAA in three different NaCl concentrations. A simple surface complexation approach is found to be very success

  9. Detection of NO2 Based on 4-Carboxyl-4'-hydroxy Azobenzene and Its Cu(Ⅱ) Complex

    Institute of Scientific and Technical Information of China (English)

    LI Jian; GONG Yun; QIN Jian-Bo; LIN Jian-Hua

    2013-01-01

    An organic ligand and its Cu(Ⅱ) complex formulated as (C13H10N2O3)·5H2O (H2L·5H2O,1) and Cu(HL)2(phen)·0.125H2O (2,H2L =4-carboxyl-4'-hydroxy azobenzene,phen =1,10-phenanthroline) have been synthesized and structurally characterized by single-crystal X-ray diffraction.In the two compounds,H2L and HL exhibit a trans-conformation.Complex 2 shows a mononuclear Cu(Ⅱ) structure with the hydroxyl group of HL uncoordinated.Complex 2 is assembled into a three-dimensional (3D) supramolecular architecture by hydrogen bonds and π-π stacking interactions,H2L and compound 2 can detect NO2 via reversible and irreversible color changes,respectively.The mechanism for the color changes is investigated.

  10. Engineering Light-Mediated Bistable Azobenzene Switches Bearing Urea d-Aminoglucose Units for Chiral Discrimination of Carboxylates.

    Science.gov (United States)

    Dąbrowa, Kajetan; Niedbała, Patryk; Jurczak, Janusz

    2016-05-01

    The symmetrical molecular receptors 1a and 1b consisting of a photochemically addressable azobenzene tether functionalized with urea hydrogen-bonding groups and d-carbohydrates as chiral selectors were developed to achieve control over the chiral recognition of α-amino acid-derived carboxylates. The photo- and thermally interconvertible planar E-1 and concaved Z-1 were found to exhibit different affinities, selectivities, and binding modes toward these biologically important anions in a highly polar medium (DMSO + 0.5% H2O). Binding affinity for the same enantiomerically pure guest was up to 3 times higher for E-1 than for Z-1 (cf. parameter β). In addition, the rate of thermal Z → E isomerization was found to depend on the chiral binding ability of Z-1, i.e., more strongly bound carboxylate enantiomer as well as higher enantiomer concentration caused faster relaxation to E-1. PMID:27057921

  11. PHOTOINDUCED BIREFRINGENCE AND NUMERICAL SOLUTION OF A NEW DYNAMIC MODEL IN AN AMORPHOUS COPOLYMER CONTAINING AZOBENZENE GROUPS

    Institute of Scientific and Technical Information of China (English)

    Ling-zhi Zhang; Zhi-gang Cai; Valerica Ninulescu; Ke Jin; Zhao-xi Liang

    2001-01-01

    Photoinduced birefringence is investigated in a new amorphous copolymer containing azobenzene groups. The levels of birefringence signal are found to depend on the polarization angle between the pump beam and the probe beam, and on the ellipticity of the pump beam. Both the growth and decay processes of the birefringence signal can be described by known biexponential equations. The rate constants and the amplitudes associated with the growth process of the photoinduced birefringence are observed to display a linear dependence with the pump beam intensity. A new dynamic model of the photoinduced birefringence is presented taking into account the contributions of both the trans and cis isomers ofazobenzene groups and the local polymer segments. The numerical treatment of this model shows good agreement with the experimental data in the whole writing-erasing processes of the photoinduced birefringence conducted in our polymer samples.

  12. Responsive behavior of 4-(N-maleimido)azobenzene in polymers with aromatic main chain and side chain linked units

    Energy Technology Data Exchange (ETDEWEB)

    Airinei, Anton; Rusu, Elena; Barboiu, Virgil, E-mail: airineia@icmpp.r [Romanian Academy, Iasi (Romania). Petru Poni Institute of Macromolecular Chemistry

    2010-07-01

    Polymer matrices with aromatic main chain and side chain linked units (polystyrene, polysulfone) were employed to construct thin films containing maleimidoazobenzene molecules in order to develop new materials with responsive properties. The photochromic behavior of the active compound was studied both in the solid and solution state for comparison. The thermal cis-trans isomerization of azobenzene chromophores in polymer films follows two different kinetic pathways. A double-exponential relaxation process (fast and slow) took place in polystyrene matrix under 70 deg C while the thermal isomerization at 70 deg C and higher follows a first-order kinetics. The cis isomer content corresponding to the photostationary state was found to be lower in polymer films than in solution. (author)

  13. 丙烯酸酯乳液胶粘剂的研究及应用%Research and application of polyacrylate emulsion adhesives

    Institute of Scientific and Technical Information of China (English)

    王善伟; 杜新胜; 徐惠俭; 柳彩霞

    2015-01-01

    综述了近年来我国丙烯酸酯乳液胶粘剂的最新研究现状,并介绍了丙烯酸酯乳液胶粘剂在压敏胶及包装材料中的应用,指出了我国丙烯酸酯乳液胶粘剂的发展方向。%The latest research situation of polyacrylate emulsion adhesives was reviewd and the application of polyacrylate emulsion adhesives in the pressure sensitive adhesives and the packaging materials was described. Finally the development trend of polyacrylate emulsion adhesives was prospected.

  14. Complex formation of Eu(III) with humic acid and polyacrylic acid

    International Nuclear Information System (INIS)

    With the intention of estimating the effect of the heterogeneous composition in the humic acid separately from its polyelectrolyte effect, comparative study on the interaction of Eu(III) with humic acid and polyacrylic acid has been carried out by the solvent extraction method with 10-3 M TTA and 10-3 M TBP in xylene at various total concentrations of Eu(III) (10-8 M to 10-5 M), pcH (5.0 to 5.5) and ionic strengths (0.02 to 1.0 M NaClO4). The interaction has been discussed in terms of the apparent complex formation constants, βα = [ML]/([M][R]), where [M] and [ML] are the concentrations of free and bound Eu3+ ion and [R] is the concentration of dissociated proton exchanging site. For both humate and polyacrylate, log βα increased with pcH or the degree of ionization and decreased with ionic strength. The Eu3+ ion concentration had no appreciable influence on the complex formation of Eu(III)-polyacrylate, and the values of log βα were obtained to be 7.57 ± 0.05 (I = 0.1, pcH = 5.53), 7.13 ± 0.04 (I = 0.1, pcH = 5.20), 6.68 ± 0.04 (I = 1.0, pcH = 5.54) and 5.61 ± 0.09 (I = 1.0, pcH = 4.73). On the other hand, log βα of humate remarkably decreased with the Eu3+ ion concentration; from 9.32 ([Eu3+] = 10-11.9 M) to 7.20 ([Eu3+] = 10-7.5 M) at pcH = 5.53 in 0.02 M NaClO4, from 8.63 ([Eu3+] = 10-12.5 M) to 6.35 ([Eu3+] = 10-7.2 M) at pcH = 5.53 in 0.1 M and from 7.59 ([Eu3+] = 10-10.7 M) to 5.20 ([Eu3+] = 10-7.0 M) at pcH = 5.52 in 1.0 M. The observed dependence of log βα of humate on the concentration of metal ion strongly suggests the heterogeneity of the complexing sites (the coexistence of weak and strong binding sites) in the humic acid. (orig.)

  15. Catalytic transfer hydrogenation of azobenzene by low-valent nickel complexes: a route to 1,2-disubstituted benzimidazoles and 2,4,5-trisubstituted imidazolines.

    Science.gov (United States)

    Zurita, Daniel A; Flores-Alamo, Marcos; García, Juventino J

    2016-06-21

    The one-pot synthesis of 1,2-disubstituted benzimidazoles by the transfer hydrogenation of azobenzene, using benzylamine as a hydrogen donor, sequential rearrangement of hydrazobenzene to semidine and further condensation with N-benzylideneamine is reported, catalyzed by 2 mol% of [Ni(COD)2] : dippe. The N2 substitution on benzimidazole can be controlled by the selection of different azobenzenes and C2 substitution will only depend on the chosen benzylamine. The current methodology avoids the addition of external oxidants, which are needed in the classical benzimidazole synthesis. In addition, the byproduct, N-benzylideneamine, obtained from dehydrogenation of benzylamine produced 2,4,5-trisubstituted imidazolines by cyclization and C-H functionalization, and this route was optimized with the use of 2 mol% of [Ni(COD)2] : 2PPh3. PMID:27254530

  16. Cascade enzymatic catalysis in poly(acrylic acid) brushes-nanospherical silica for glucose detection.

    Science.gov (United States)

    Zhao, Yan; Wang, Ying; Zhang, Xiaobin; Kong, Rongmei; Xia, Lian; Qu, Fengli

    2016-08-01

    The ultrasensitive monitoring of glucose with a fast and accurate method is significant in potential therapeutics and optimizes protein biosynthesis. Incorporation of enzyme into matrix is considered as promising candidates for constructing highly sensitive glucose-responsive systems. In this study, three-dimensional poly(acrylic acid) brushes-nanospherical silica (PAA-nano silica) with high amplification capability and stability were used to covalently immobilize bienzymes for cascade enzymatic catalysis. The major advantages of PAA-nano silica-bienzyme co-incorporation is that the enzymes are proximity distribution, and such close confinement both minimized the diffusion of intermediates among the enzymes in the consecutive reaction and improve the utilization efficiency of enzymes, thereby enhancing the overall reaction efficiency and specificity. Thus, this present bienzymatic biosensor shows robust signal amplification and ultrasensitivity of glucose-responsive properties with a detection limit of 0.04μM. PMID:27216683

  17. IMMOBILIZATION OF GLUCOSE OXIDASE AND CELLULASE BY CHITOSAN-POLYACRYLIC ACID COMPLEX

    Institute of Scientific and Technical Information of China (English)

    WANG Lingzhi; JIANG Yingyan; ZHANG Changde; HUANG Dexiu

    1990-01-01

    This study is concerned with chitosan-polyacrylic acid complex as a carrier to immobilize glucose oxidase (GOD) and cellulase. The optimum temperature of the immobilized GOD (IG) was determined to be 60 ℃ which is higher than that of the native GOD about 40 ℃ . The optimum temperature of the immobilized cellulase (IC) was determined to be about 30 ℃ higher than that of native cellulase. Both of the optimum pH of IG and IC shifted one pH unit to acid. Immobilized enzyme may be used in more wide pH range. Their storage life are much longer compared with their native states. Both of them can be reused at least 12 times.

  18. Effects of postthermal treatment and UV irradiation on the structure of titania-polyacrylate nanocomposites

    Institute of Scientific and Technical Information of China (English)

    Tao Wan; Fei Feng; Yuechuan Wang

    2006-01-01

    The effects of postthermal treatment and irradiation time on the structure and thermal stability of TiO2/polyacrylate nanocomposites by a sol-gel process in reverse micelles and subsequent rapid photopolymerization were investigated, and the hybrid films were characterized by thermal gravimetry analysis (TGA), X-ray photoelectron spectrum (XPS), and atomic force microscopy (AFM).XPS data suggested that the prolongation of irradiation time and the postthermal treatment promoted titania formation, with the former affecting more remarkably. TGA data showed that TiO2-hybrid films could upgrade the decomposition onset temperature (Tonset) as well as the temperature at which there is a maximum mass loss rate (Tmax). AFM data demonstrated that the inorganic titania particles with a mean diameter of 25.26-28.84 nm were homogeneously distributed in the organic matrix.

  19. Isomerization and fluorescence depolarization of merocyanine 540 in polyacrylic acid. Effect of H

    Indian Academy of Sciences (India)

    Dipankar Sukul; Sobhan Sen; Partha Dutta; Kankan Bhattacharyya

    2002-10-01

    Dynamics of isomerization and fluorescence depolarization of merocyanine 540 (MC540) in an aqueous solution of polyacrylic acid (PAA) have been studied using picosecond time resolved fluorescence spectroscopy. It is observed that the dynamics of isomerization and depolarization are sensitive enough to monitor the uncoiling of PAA at high H (> 6). At low H (< 3), when the polymer remains in a hypercoiled form, polymer bound MC540 experiences very high microscopic friction and, hence, the isomerization and depolarization processes are very slow. At high H (> 6) a polyanion is formed and the polymer assumes an extended configuration due to electrostatic repulsion. At high H (> 6), the anionic probe MC540 is expelled from the polyanion to bulk water and the dynamics of isomerization and fluorescence depolarization become faster by 12 and 5 times respectively, compared to those at low H.

  20. CHOLESTERIC LIQUID CRYSTALLINE CHARACTER ON THE SURFACE OF CHITOSAN/POLYACRYLIC ACID COMPOSITES

    Institute of Scientific and Technical Information of China (English)

    Yan-ming Dong; Yu-song; Wu Mian Wang

    2001-01-01

    The cholesteric liquid crystalline structure in chitosan/polyacrylic acid composite films was studied by surface techniques. A periodical lamellar-like structure was observed in the permanganic acid etched film surface by both scanning electron microscopy (SEM) and atomic force microscopy (AFM), instead of the thumb-print texture which can be detected with polarized optical microscopy. It is suggested that the periodical lamellar-like structure is induced by the etching selectivity between cholesteric layers due to different molecular arrangement on the film surface. Four kinds of perpendicular disclinations, I.e. Χ→τ- + λ+, χ→λ- + τ+, χ→τ- + τ+ and χ→λ- + λ+, were found in the composite films from SEM observations. The smallest periodicity of lamellar-like structure (equals to halfpitch) is 20~40 nm measured with AFM.

  1. Poly-Acrylic Acid Derivatives as Diesel Flow Improver for Paraffin-Based Daqing Diesel

    Institute of Scientific and Technical Information of China (English)

    Cuiyu Jiang; Ming Xu; Xiaoli Xi; Panlun Qi; Hongyan Shang

    2006-01-01

    Since the diesel products from paraffin-based Daqing crude oil showed low sensitivity to certain commercial diesel pour point depressant (PPDs) that resulted from the high content of paraffin, certain poly-acrylic acid derivatives (PADE) with-COOR,-COOH,-CONHR, and -COO-NH3+R groups by molecular design on the mechanics of diesel; PPDs were synthesized and evaluated as cold flow improver for Daqing 0# diesel in this paper. The pure PADE was superior to the commercial PPDs and displayed a substantial ability of wax crystals dispersion. There was a synergistic effect among the PADE and T1804 and secondary amine. The synergism clearly improved the low temperature performance of Daqing diesel products and could reduce the cold filter plugging point of 0# diesel by 6-7 ℃.

  2. ABS polymer electroless plating through a one-step poly(acrylic acid) covalent grafting.

    Science.gov (United States)

    Garcia, Alexandre; Berthelot, Thomas; Viel, Pascal; Mesnage, Alice; Jégou, Pascale; Nekelson, Fabien; Roussel, Sébastien; Palacin, Serge

    2010-04-01

    A new, efficient, palladium- and chromium-free process for the electroless plating of acrylonitrile-butadiene-styrene (ABS) polymers has been developed. The process is based on the ion-exchange properties of poly(acrylic acid) (PAA) chemically grafted onto ABS via a simple and one-step method that prevents using classical surface conditioning. Hence, ABS electroless plating can be obtained in three steps, namely: (i) the grafting of PAA onto ABS, (ii) the copper Cu(0) seeding of the ABS surface, and (iii) the nickel or copper metallization using commercial-like electroless plating bath. IR, XPS, and SEM were used to characterize each step of the process, and the Cu loading was quantified by atomic absorption spectroscopy. This process successfully compares with the commercial one based on chromic acid etching and palladium-based seed layer, because the final metallic layer showed excellent adhesion with the ABS substrate. PMID:20361751

  3. Preparation of poly(acrylic acid) particles by dispersion polymerization in an ionic liquid.

    Science.gov (United States)

    Minami, Hideto; Kimura, Akira; Kinoshita, Keigo; Okubo, Masayoshi

    2010-05-01

    Poly(acrylic acid) (PAA) particles were successfully prepared by dispersion polymerization of acrylic acid in ionic liquid, N,N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium bis(trifluoro-methanesulfonyl)amide ([DEME][TFSA]) at 70 degrees C with low hydrolysis grade (35.4%) poly(vinyl alcohol) as stabilizer. Interestingly, the PAA particles were easily extracted as particle state with water. Thus, the PAA particles had a cross-linked structure during the polymerization without cross-linker. Moreover, it was also noted that the cross-linking density of the PAA particles could be controlled by thermal treatment at various temperatures in [DEME][TFSA] utilizing the advantages of nonvolatility and high thermal stability of the ionic liquid. PMID:20043688

  4. Wheat Gluten Blends with Maleic Anhydride-Functionalized Polyacrylate Cross-Linkers for Improved Properties.

    Science.gov (United States)

    Diao, Cheng; Xia, Hongwei; Parnas, Richard S

    2015-10-14

    A family of polyacrylate-based cross-linkers was synthesized to maximize the toughness of high Tg, high modulus wheat gluten blends in the glassy state. Mechanical testing and damping measurements were conducted to provide an example where the work of fracture and strength of the blend substantially exceeds polystyrene while maintaining flexure stiffness in excess of 3 GPa. The new rubbery cross-linkers, polymethyl acrylate-co-maleic anhydride and polyethyl acrylate-co-maleic anhydride, improve WG mechanical properties and reduce water absorption simultaneously. MDSC, FTIR, HPLC, and NMR data confirmed the cross-linking reaction with wheat gluten. Flexural, DMA, and water absorption testing were carried out to characterize the property improvements. DMA was conducted to investigate the relationship between energy damping and mechanical property improvement. If the cross-linker damping temperature is close to the testing temperature, the entire sample exhibits high damping, toughness, and strength. PMID:26394179

  5. Poly(acrylic acid)-stabilized colloidal gold nanoparticles: synthesis and properties

    International Nuclear Information System (INIS)

    Combining the intriguing optical properties of gold nanoparticles with the inherent physical and dynamic properties of polymers can give rise to interesting hybrid nanomaterials. In this study, we report the synthesis of poly(acrylic acid) (PAA)-capped gold nanoparticles. The polyelectrolyte-wrapped gold nanoparticles were fully characterized and studied via a combination of techniques, i.e. UV-vis and infrared spectroscopy, dark field optical microscopy, SEM imaging, dynamic light scattering and zeta potential measurements. Although PAA-capped nanoparticles have been previously reported, this study revealed some interesting aspects of the colloidal stability and morphological change of the polymer coating on the nanoparticle surface in an electrolytic environment, at various pH values and at different temperatures.

  6. Effects of sodium polyacrylate on water retention and infiltration capacity of a sandy soil.

    Science.gov (United States)

    Zhuang, Wenhua; Li, Longguo; Liu, Chao

    2013-01-01

    Based on the laboratory study, the effects of sodium polyacrylate (SP) was investigated at 5 rates of 0, 0.08, 0.2, 0.5, and 1%, on water retention, saturated hydraulic conductivity(Ks), infiltration characteristic and water distribution profiles of a sandy soil. The results showed that water retention and available water capacity effectively increased with increasing SP rate. The Ks and the rate of wetting front advance and infiltration under certain pond infiltration was significantly reduced by increasing SP rate, which effectively reduced water in a sandy soil leaking to a deeper layer under the plough layer. The effect of SP on water distribution was obviously to the up layer and very little to the following deeper layers. Considering both the effects on water retention and infiltration capacity, it is suggested that SP be used to the sandy soil at concentrations ranging from 0.2 to 0.5%. PMID:24701379

  7. Methods for purifying and detoxifying sodium dodecyl sulfate-stabilized polyacrylate nanoparticles.

    Science.gov (United States)

    Garay-Jimenez, Julio C; Young, Ashley; Gergeres, Danielle; Greenhalgh, Kerriann; Turos, Edward

    2008-06-01

    Recent research in our laboratory has centered on studies of polyacrylate and polyacrylamide nanoparticle emulsions for use in antibiotic delivery. Our goal is to develop these nanoparticle emulsions for treatment of life-threatening bacterial infections such as those caused by methicillin-resistant Staphylococcus aureus. For this intended application it is necessary to ensure that the biological activity of the emulsion is due only to the drug attached to the polymeric chain and not to any extraneous components. To investigate this we evaluated cytotoxicity and microbiological activity of the nanoparticle emulsions before and after purification by centrifugation, dialysis, and gel filtration. Depending on the amount of surfactant used, all or most of the microbial and cellular toxicity can be removed by a simple purification procedure. PMID:18472305

  8. Preparation and characterization of interpenetrating networks based on polyacrylates and poly(lactic acid

    Directory of Open Access Journals (Sweden)

    H. Kaczmarek

    2012-01-01

    Full Text Available Three different, multifunctional acrylic monomers were photopolymerized in a matrix of poly(lactic acid, PLA, using 2-hydroxy-2-methyl-1-phenyl-propan-1-one as a photoinitiator. The kinetics of the photopolymerization of monomers in PLA, studied with Fourier Transform Infrared Spectroscopy, has been compared to analogous processes of pure monomers under the same conditions (room temperature, air atmosphere. Additionally, poly(ethylene glycol was added to acrylate/PLA blends as plasticizer.The highly crosslinked networks obtained were characterized by FTIR and optical microscopy. The amount of insoluble gel has been estimated gravimetrically. It was found that the studied systems are characterized by very high polymerization rate, moreover, efficient grafting of polyacrylates on PLA takes place. The observed morphology indicates the heterogeneity of formed networks. The glass transition temperature of PLA in studied blends has been determined by differential scanning calorimetry.

  9. Endoscopic treatment of vesicoureteral reflux with polyacrylate polyalcohol copolymer and dextranomer/hyaluronic acid in adults

    Directory of Open Access Journals (Sweden)

    Akif Turk

    2014-06-01

    Full Text Available Purpose Aim of this study is to examine the effectiveness of dextranomer/hyaluronic acid copolymer and polyacrylate polyalcohol copolymer in endoscopic treatment of vesicoureteral reflux disease in adult patients with and without chronic renal failure. Materials and Methods Thirty two patients (12 female, 20 male with a total of 50 renal units were treated for vesicoureteral reflux. There were 26 (81% chronic renal failure patients. The success of treatment was evaluated by voiding cystouretrography at 3rd and 12th months after subureteric injection. The persistence of reflux was considered as failure. Patients were divided into two groups according to injected material. Age, sex, grade of reflux and treatment results were recorded and evaluated. Results Reflux was scored as grade 1 in seven (14%, grade 2 in 16 (32%, grade 3 in 21 (42% and grade 4 in six (12% renal units. There was not patient with grade 5 reflux. Fourteen renal units (28% were treated with dextranomer/hyaluronic acid copolymer (group 1 and 36 renal units (72% were treated with polyacrylate polyalcohol copolymer (group 2. The overall treatment success was achieved at 40 renal units (80%. The treatment was successful at 11 renal units (79% in group 1 and 29 renal units (81% in group 2 (p = 0.71. There was not statistically significant difference between two groups with patients with chronic renal failure in terms of treatment success (p = 1.00. Conclusions The effectiveness of two bulking agents was similar in treatment of vesicoureteral reflux disease in adult patients and patients with chronic renal failure.

  10. Cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate copolymer

    Directory of Open Access Journals (Sweden)

    Lee KD

    2013-08-01

    Full Text Available Kyung Dong Lee,1,* Young-Il Jeong,2,* Da Hye Kim,3,4 Gyun-Taek Lim,2 Ki-Choon Choi5 1Department of Oriental Medicine Materials, Dongshin University, Naju, South Korea; 2Department of Polymer Engineering, Chonnam National University, Gwangju, South Korea; 3Faculty of Life and Environmental Science, Shimane University, Matsue, Japan; 4United Graduate School of Agricultural Sciences, Tottori University, Tottori, Japan; 5Grassland and Forages Division, National Institute of Animal Science, Rural Development Administration, Cheonan, South Korea *These authors contributed equally to this work Background: Although cisplatin is extensively used in the clinical field, its intrinsic toxicity limits its clinical use. We investigated nanoparticle formations of poly(acrylic acid-co-methyl methacrylate (PAA-MMA incorporating cisplatin and their antitumor activity in vitro and in vivo. Methods: Cisplatin-incorporated nanoparticles were prepared through the ion-complex formation between acrylic acid and cisplatin. The anticancer activity of cisplatin-incorporated nanoparticles was assessed with CT26 colorectal carcinoma cells. Results: Cisplatin-incorporated nanoparticles have small particle sizes of less than 200 nm with spherical shapes. Drug content was increased according to the increase of the feeding amount of cisplatin and acrylic acid content in the copolymer. The higher acrylic acid content in the copolymer induced increase of particle size and decrease of zeta potential. Cisplatin-incorporated nanoparticles showed a similar growth-inhibitory effect against CT26 tumor cells in vitro. However, cisplatin-incorporated nanoparticles showed improved antitumor activity against an animal tumor xenograft model. Conclusion: We suggest that PAA-MMA nanoparticles incorporating cisplatin are promising carriers for an antitumor drug-delivery system. Keywords: cisplatin, nanoparticle, poly(acrylic acid-co-methyl methacrylate, ion complexes

  11. Polyethylenimine-polyacrylic acid nanocomposites: Type of bonding does influence the gene transfer efficacy and cytotoxicity.

    Science.gov (United States)

    Tripathi, Sushil K; Ahmadi, Zeba; Gupta, Kailash C; Kumar, Pradeep

    2016-04-01

    The main aim of the current study is to compare the physicochemical properties, cytotoxicity and gene-transfer ability of electrostatically and covalently linked nanocomposites of polyethylenimine (PEI) and polyacrylic acid (PAA) on mammalian cells. Two series of nanocomposites, ionic PEI-PAA (iPP) and covalent PEI-PAA (cPP), were synthesized by varying the amounts of polyacrylic acid (PAA). Physicochemical characterization revealed that iPP nanopcomposites were of bigger sized than cPP nanocomposites with zeta potential almost comparable. Nucleic acid binding assay displayed that iPP and cPP nanocomposites, having sufficient cationic charge, efficiently interacted with plasmid DNA and completely retarded its electrophoretic mobility on agarose gel. In vitro MTT assay showed slightly higher cell viability of cPP/pDNA complexes over their ionic counterparts. Both the series of nanocomposite/pDNA complexes exhibited considerably higher transfection efficacy compared to pDNA complexes of native bPEI and the standard transfection reagent, Lipofectamine, with cPP/pDNA complexes performed much better than iPP/pDNA complexes. Flow cytometry further confirmed these findings where cPP-4/pDNA complex showed transfection in ∼85% HEK293 cells, while iPP-2/pDNA complex transfected ∼67% HEK293 cells. Lipofectamine/pDNA and bPEI/pDNA complexes could transfect just ∼35% and ∼26% HEK293 cells. All these results demonstrate the superiority of covalently linked nanocomposites (cPP) which could be used as efficient carriers for nucleic acids in future gene delivery applications. PMID:26745638

  12. Magnetic hyperthermia studies on water-soluble polyacrylic acid-coated cobalt ferrite nanoparticles

    International Nuclear Information System (INIS)

    We report on synthesis and hyperthermia studies in the water-soluble ferrofluid made of polyacrylic acid-coated cobalt ferrite (CoFe2O4) nanoparticles with different particle sizes. Magnetic nanoparticles were synthesized using co-precipitation method and particle size was varied as 6, 10, and 14 nm by varying the precursor to surfactant concentration. PAA surfactant bonding and surfactant thickness were studied by FTIR and thermogravimetric analysis. At room temperature, nanoparticles show superparamagnetism and saturation magnetization was found to vary from 33 to 44 emu/g with increase in the particle size from 6 to 14 nm, and this increase was attributed to the presence of a magnetic inert layer of 4 Å thick. Effect of particle size, concentration, and alternating magnetic field strength at 275 kHz on specific absorption rate were studied by preparing ferrofluids in deionized water at different concentrations. Ferrofluids at a concentration of 1.25 g/L, with 10 min of AMF exposure of strength ∼15.7 kA/m show stable temperatures ∼48, 58, and 68 °C with increase in the particle sizes 6, 10, and 14 nm. A maximum specific absorption rate of 251 W/g for ferrofluid with a particle size of 10 nm at 1.25 g/L, 15.7 kA/m, and 275 kHz was observed. Viability of L929 fibroblasts is measured by MTT assay cytotoxicity studies using the polyacrylic acid-coated CoFe2O4 nanoparticles

  13. Magnetic hyperthermia studies on water-soluble polyacrylic acid-coated cobalt ferrite nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Krishna Surendra, M. [Indian Institute of Technology Madras, Department of Physics, Nano Functional Materials Technology Centre, Materials Research Centre (India); Annapoorani, S. [Anna University of Technology, Department of Nanotechnology (India); Ansar, Ereath Beeran; Harikrishna Varma, P. R. [Sree Chitra Tirunal Institute for Medical Sciences and Technology, Bioceramics Laboratory (India); Ramachandra Rao, M. S., E-mail: msrrao@iitm.ac.in [Indian Institute of Technology Madras, Department of Physics, Nano Functional Materials Technology Centre, Materials Research Centre (India)

    2014-12-15

    We report on synthesis and hyperthermia studies in the water-soluble ferrofluid made of polyacrylic acid-coated cobalt ferrite (CoFe{sub 2}O{sub 4}) nanoparticles with different particle sizes. Magnetic nanoparticles were synthesized using co-precipitation method and particle size was varied as 6, 10, and 14 nm by varying the precursor to surfactant concentration. PAA surfactant bonding and surfactant thickness were studied by FTIR and thermogravimetric analysis. At room temperature, nanoparticles show superparamagnetism and saturation magnetization was found to vary from 33 to 44 emu/g with increase in the particle size from 6 to 14 nm, and this increase was attributed to the presence of a magnetic inert layer of 4 Å thick. Effect of particle size, concentration, and alternating magnetic field strength at 275 kHz on specific absorption rate were studied by preparing ferrofluids in deionized water at different concentrations. Ferrofluids at a concentration of 1.25 g/L, with 10 min of AMF exposure of strength ∼15.7 kA/m show stable temperatures ∼48, 58, and 68 °C with increase in the particle sizes 6, 10, and 14 nm. A maximum specific absorption rate of 251 W/g for ferrofluid with a particle size of 10 nm at 1.25 g/L, 15.7 kA/m, and 275 kHz was observed. Viability of L929 fibroblasts is measured by MTT assay cytotoxicity studies using the polyacrylic acid-coated CoFe{sub 2}O{sub 4} nanoparticles.

  14. Low Light CMOS Contact Imager with an Integrated Poly-Acrylic Emission Filter for Fluorescence Detection

    Directory of Open Access Journals (Sweden)

    Yonathan Dattner

    2010-05-01

    Full Text Available This study presents the fabrication of a low cost poly-acrylic acid (PAA based emission filter integrated with a low light CMOS contact imager for fluorescence detection. The process involves the use of PAA as an adhesive for the emission filter. The poly-acrylic solution was chosen due its optical transparent properties, adhesive properties, miscibility with polar protic solvents and most importantly its bio-compatibility with a biological environment. The emission filter, also known as an absorption filter, involves dissolving an absorbing specimen in a polar protic solvent and mixing it with the PAA to uniformly bond the absorbing specimen and harden the filter. The PAA is optically transparent in solid form and therefore does not contribute to the absorbance of light in the visible spectrum. Many combinations of absorbing specimen and polar protic solvents can be derived, yielding different filter characteristics in different parts of the spectrum. We report a specific combination as a first example of implementation of our technology. The filter reported has excitation in the green spectrum and emission in the red spectrum, utilizing the increased quantum efficiency of the photo sensitive sensor array. The thickness of the filter (20 μm was chosen by calculating the desired SNR using Beer-Lambert’s law for liquids, Quantum Yield of the fluorophore and the Quantum Efficiency of the sensor array. The filters promising characteristics make it suitable for low light fluorescence detection. The filter was integrated with a fully functional low noise, low light CMOS contact imager and experimental results using fluorescence polystyrene micro-spheres are presented.

  15. Supramolecular Phase-Selective Gelation by Peptides Bearing Side-Chain Azobenzenes: Effect of Ultrasound and Potential for Dye Removal and Oil Spill Remediation

    OpenAIRE

    Jürgen Bachl; Stefan Oehm; Judith Mayr; Carlos Cativiela; José Juan Marrero-Tellado; David Díaz Díaz

    2015-01-01

    Phase selective gelation (PSG) of organic phases from their non-miscible mixtures with water was achieved using tetrapeptides bearing a side-chain azobenzene moiety. The presence of the chromophore allowed PSG at the same concentration as the minimum gelation concentration (MGC) necessary to obtain the gels in pure organic phases. Remarkably, the presence of the water phase during PSG did not impact the thermal, mechanical, and morphological properties of the corresponding organogels. In the ...

  16. 石墨烯/偶氮杂化材料研究进展%Progress on graphene/azobenzene hybrid materials

    Institute of Scientific and Technical Information of China (English)

    王东瑞; 王晓工

    2012-01-01

    Graphene, a true two dimensional nanomaterial with the layer thickness of one atom, has showed many outstanding properties and aroused tremendous research enthusiasm. Azobenzene-containing polymers and other materials have also attracted considerable attention because of the unique photoresponsive properties. Graphene/ azobenzene hybrids materials can combine interesting properties of graphere and azobenzene-containing materials and have been studied in authors and other laboratories in recent years. This review highlighted some recent research progresses in this area. The content of this article included the preparations of graphene/azobenzene hybrids materials through surface-grafting of azo polymers, covalent-bonding modification with low-molecular-weight azo compounds and electrostatic layer-by-layer deposition. The photoresponsive properties and application in the electronchemical energy storage device of the materials were also reviewed in some detail.%石墨烯作为一种新型二维平面纳米材料,表现出许多优异的物理性质.含偶氮苯的化合物和聚合物作为功能材料具有独特的光响应性质.将石墨烯的特性与偶氮材料的光响应性相结合,有望发展一类具有卓越性能的新型光电功能材料.本文总结了石墨烯/偶氮杂化材料这一研究方向的最新进展,重点介绍了杂化材料的制备、表征和光电功能性质等,并简要展望了这类材料的发展前景.

  17. The influence of poly(acrylic) acid number average molecular weight and concentration in solution on the compressive fracture strength and modulus of a glass-ionomer restorative.

    LENUS (Irish Health Repository)

    Dowling, Adam H

    2011-06-01

    The aim was to investigate the influence of number average molecular weight and concentration of the poly(acrylic) acid (PAA) liquid constituent of a GI restorative on the compressive fracture strength (σ) and modulus (E).

  18. Symmetrical trimeric star-shaped mesogens based on 1,3,5-trisubstituted benzene incorporating Schiff base and azobenzene fragments as the peripheral units: Synthesis and mesomorphic properties

    Indian Academy of Sciences (India)

    Guan-Yeow Yeap; Yew-Hong Ooi; Nozomi Uchida; Masato M Ito

    2014-05-01

    Two series of symmetrical three-armed star-shaped mesogens based on 1,3,5-trihydroxybenzene as a core unit, interconnecting three Schiff base or azobenzene moieties via oxymethylene spacers have been synthesized and characterized by spectroscopic techniques. Every member in these series possesses either chlorine (Cl) or bromine (Br) terminal atom, with different alkyl spacer length (CH2 whereby ranging from 3 to 6). Their thermal stability and mesomorphic properties are investigated by employing DSC and POM. The dependence of phase transition in relation to the alkyl spacer length is shown by both series. These star-shaped mesogens exhibit only nematic and smectic phases. The difference between the two series lies on the structure of linking group in the peripheral units (-CH=N- for series PSB-X- and -N=N- for series PAZ-X-). Therefore, a comparison study of the mesomorphic properties between these two series of star-shaped mesogens is discussed whereby the azobenzene-basedmesogens are thermally more stable than the Schiff base counterpart. In addition, soft crystalline phase is observed for the azobenzene-based star-shaped mesogens possessing hexyl alkyl spacer.

  19. Synthesis and characterization of nano-SiO2 modified fluorine-containing polyacrylate emulsifier-free emulsion

    International Nuclear Information System (INIS)

    Graphical abstract: Nano-SiO2 modified fluorine-containing polyacrylate emulsifier-free emulsion was synthesized by emulsifier-free emulsion polymerization and sol–gel process using ethyl silicate as precursor for nano-SiO2. - Highlights: • Nano-SiO2 modified fluorine-containing polyacrylate emulsifier-free emulsion was successfully synthesized by emulsion polymerization using surfmer and sol–gel process. • The contact angle results showed that the finished fabric had an excellent water and oil repellency. • The nano-SiO2 modified fluorine-containing polyacrylate emulsifier-free emulsion proved to be highly solvent-resistant and water-resistant. • The transmission electron microscopy (TEM) indicated that the nano-SiO2 presented on the surface of latex particles. • The atomic force microscope (AFM) and energy dispersive X-ray spectrometer (EDX) confirmed that the hybrid film had a rough surface and the organic fluorine segment could migrate onto the film–air interface. - Abstract: Nano-SiO2 modified fluorine-containing polyacrylate emulsifier-free emulsion, consisting of methyl methacrylate, butyl acrylate, dodecafluoroheptyl methacrylate and ethyl silicate, was successfully synthesized by emulsion polymerization using surfmer and sol–gel process. When increasing ethyl silicate content, the latex centrifugal stability decreased, and the latex particle size increased. The contact angle results showed that the finished fabric had an excellent water and oil repellency. Furthermore, compared with fluorine-containing polyacrylate emulsifier-free emulsion, the obtained nano-SiO2 modified fluorine-containing polyacrylate emulsifier-free emulsion proved to be highly solvent-resistant and water-resistant. In addition, the transmission electron microscopy (TEM) indicated that the nano-SiO2 presented on the surface of latex particles. The atomic force microscope (AFM) and energy dispersive X-ray spectrometer (EDX) confirmed that the hybrid film had a rough

  20. Synthesis and characterization of nano-SiO{sub 2} modified fluorine-containing polyacrylate emulsifier-free emulsion

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Jianhua, E-mail: zhoujianh@21cn.com [College of Resource and Environment, Shaanxi University of Science and Technology, Xi’an 710021 (China); Shaanxi Research Institute of Agricultural Products Processing Technology, Xi’an 710021 (China); Chen, Xin; Duan, Hao; Ma, Jianzhong; Ma, Yurong [College of Resource and Environment, Shaanxi University of Science and Technology, Xi’an 710021 (China)

    2015-03-15

    Graphical abstract: Nano-SiO{sub 2} modified fluorine-containing polyacrylate emulsifier-free emulsion was synthesized by emulsifier-free emulsion polymerization and sol–gel process using ethyl silicate as precursor for nano-SiO{sub 2}. - Highlights: • Nano-SiO{sub 2} modified fluorine-containing polyacrylate emulsifier-free emulsion was successfully synthesized by emulsion polymerization using surfmer and sol–gel process. • The contact angle results showed that the finished fabric had an excellent water and oil repellency. • The nano-SiO{sub 2} modified fluorine-containing polyacrylate emulsifier-free emulsion proved to be highly solvent-resistant and water-resistant. • The transmission electron microscopy (TEM) indicated that the nano-SiO{sub 2} presented on the surface of latex particles. • The atomic force microscope (AFM) and energy dispersive X-ray spectrometer (EDX) confirmed that the hybrid film had a rough surface and the organic fluorine segment could migrate onto the film–air interface. - Abstract: Nano-SiO{sub 2} modified fluorine-containing polyacrylate emulsifier-free emulsion, consisting of methyl methacrylate, butyl acrylate, dodecafluoroheptyl methacrylate and ethyl silicate, was successfully synthesized by emulsion polymerization using surfmer and sol–gel process. When increasing ethyl silicate content, the latex centrifugal stability decreased, and the latex particle size increased. The contact angle results showed that the finished fabric had an excellent water and oil repellency. Furthermore, compared with fluorine-containing polyacrylate emulsifier-free emulsion, the obtained nano-SiO{sub 2} modified fluorine-containing polyacrylate emulsifier-free emulsion proved to be highly solvent-resistant and water-resistant. In addition, the transmission electron microscopy (TEM) indicated that the nano-SiO{sub 2} presented on the surface of latex particles. The atomic force microscope (AFM) and energy dispersive X-ray spectrometer

  1. Modification method and applications of polyacrylic supperabsorbents%聚丙烯酸类高吸水性树脂的改性方法及应用

    Institute of Scientific and Technical Information of China (English)

    谢洋; 付东; 隋新; 李鹏; 杨帆

    2014-01-01

    In this review,the modification,development direction and application fields of polyacrylic supperabsorbents are introduced in detail. The research trend and development direction of polyacrylic supperabsorbents are also involved.%对聚丙烯酸类高吸水性树脂的改性方法、发展方向及应用领域进行了详细的介绍,并对其研究发展方向进行了展望。

  2. Influence of He/O2 atmospheric pressure plasma jet treatment on subsequent wet desizing of polyacrylate on PET fabrics

    International Nuclear Information System (INIS)

    The influence of He/O2 atmospheric pressure plasma jet (APPJ) treatment on subsequent wet desizing of polyacrylate on PET fabrics was studied in the present paper. Weight loss results indicated that the weight loss increased with an increase of plasma treatment time. Atomic force microscopy (AFM) and scanning electron microscopy (SEM) showed an increased surface roughness after the plasma treatment. SEM also showed that the fiber surfaces were as clean as unsized fibers after 35 s treatment followed by NaHCO3 desizing. X-ray photoelectron spectroscopy (XPS) analysis indicated that oxygen-based functional groups increased for the plasma treated polyacrylate sized fabrics. The percent desizing ratio (PDR) results showed that more than 99% PDR was achieved after 65 s plasma treatment followed by a 5 min NaHCO3 desizing. Compared to conventional wet desizing, indicating that plasma treatment could significantly reduce desizing time.

  3. Poly(acrylic acid) interpolymer complexation: use of a fluorescence time resolved anisotropy as a poly(acrylamide) probe

    OpenAIRE

    Swift, T.; Swanson, L; Rimmer, S.

    2014-01-01

    A low concentration poly(acrylamide) sensor has been developed which uses the segmental mobility of another polymer probe with a covalently attached fluorescent marker. Interpolymer complexation with poly(acrylic acid) leads to reduced segmental mobility which can be used to determine the concentration of polymer in solution. This technique could be useful in detecting the runoff of polymer dispersants and flocculants in fresh water supplies following water purification processes

  4. Blood-Vessel Mimicking Structures by Stereolithographic Fabrication of Small Porous Tubes Using Cytocompatible Polyacrylate Elastomers, Biofunctionalization and Endothelialization

    OpenAIRE

    Birgit Huber; Sascha Engelhardt; Wolfdietrich Meyer; Hartmut Krüger; Annika Wenz; Veronika Schönhaar; Tovar, Günter E. M.; Kluger, Petra J.; Kirsten Borchers

    2016-01-01

    Blood vessel reconstruction is still an elusive goal for the development of in vitro models as well as artificial vascular grafts. In this study, we used a novel photo-curable cytocompatible polyacrylate material (PA) for freeform generation of synthetic vessels. We applied stereolithography for the fabrication of arbitrary 3D tubular structures with total dimensions in the centimeter range, 300 µm wall thickness, inner diameters of 1 to 2 mm and defined pores with a constant diameter of appr...

  5. Rapid 3D Patterning of Poly(acrylic acid) Ionic Hydrogel for Miniature pH Sensors.

    Science.gov (United States)

    Yin, Ming-Jie; Yao, Mian; Gao, Shaorui; Zhang, A Ping; Tam, Hwa-Yaw; Wai, Ping-Kong A

    2016-02-17

    Poly(acrylic acid) (PAA), as a highly ionic conductive hydrogel, can reversibly swell/deswell according to the surrounding pH conditions. An optical maskless -stereolithography technology is presented to rapidly 3D pattern PAA for device fabrication. A highly sensitive miniature pH sensor is demonstrated by in situ printing of periodic PAA micropads on a tapered optical microfiber. PMID:26643765

  6. The Fouling of Zirconium(IV) Hydrous Oxide–Polyacrylate Dynamically Formed Membranes during the Nanofiltration of Lactic Acid Solutions

    OpenAIRE

    Ewa Polom

    2013-01-01

    The results of investigations of flux decline during nanofiltration (NF) of lactic acid solutions using dynamically formed zirconium(IV) hydrous oxide/polyacrylate membranes (Zr(IV)/PAA) under conditions resulting in low and high lactic acid rejection are reported. The experimental permeate flux versus time curves were analyzed in the frame of resistance in a series model with the aim of developing the characteristic of resistances. Analysis of experimental data and results of calculations sh...

  7. Influence of polyacrylic acid nanoparticles on the elastic properties of RBCs membranes in patients with diabetes mellitus type 2

    Czech Academy of Sciences Publication Activity Database

    Melnikova, G.B.; Kuzhel, N.S.; Tolstaya, T.N.; Konstantinova, E.E.; Drozd, E.S.; Shisko, O.N.; Mokhort, T.G.; Antonova, N.; Říha, Pavel; Kowalczuk, A.; Koseva, N.

    2015-01-01

    Roč. 29, č. 4 (2015), s. 12-19. ISSN 1313-2458 Institutional support: RVO:67985874 Keywords : red blood cells * nanoparticles * poly(acrylic acid) * elasticity modulus * atomic force microscopy Subject RIV: BK - Fluid Dynamics http://www.imbm.bas.bg/biomechanics/uploads/Archive2015-4/12-19_Melnikova-Konstantinova_et%20al_abstract-1_18.12.15.pdf

  8. NMR Water Self–Diffusion and Relaxation Studies on Sodium Polyacrylate Solutions and Gels in Physiologic Ionic Solutions

    OpenAIRE

    Bai, Ruiliang; Basser, Peter J.; Briber, Robert M.; Horkay, Ferenc

    2013-01-01

    Water self-diffusion coefficients and longitudinal relaxation rates in sodium polyacrylate solutions and gels were measured by NMR, as a function of polymer content and structure in a physiological concentration range of monovalent and divalent cations, Ca2+ and Na+. Several physical models describing the self-diffusion of the solvent were applied and compared. A free-volume model was found to be in good agreement with the experimental results over a wide range of polymer concentrations. The ...

  9. Influence of ammonia and water sorption on the chemical and electrochemical properties of polyacrylic acid and its derivates

    OpenAIRE

    Hörter, Melanie

    2008-01-01

    The main achievement of this research work is the elaboration of a phenomenological model that describes water vapour and ammonia gas sorption into polyacrylic acid (PAA) films and explains the associated changes of their chemical and electrochemical properties; it was successfully confronted with experimental results either gathered during the author’s work or previously published. By allowing a deeper understanding of sensing, the model will help further developments of PAA as a material fo...

  10. Evaluation of the Physical Stability of Zinc Oxide Suspensions Containing Sodium Poly-(acrylate) and Sodium Dodecylsulfate

    OpenAIRE

    Chabni, Malika; Bougherra, Hadda; Lounici, Hakim; Ahmed-Zaïd, Toudert; Canselier, Jean-Paul; Bertrand, Joël

    2011-01-01

    The physical stability of zinc oxide (ZnO) aqueous suspensions has been monitored during two months by different methods of investigation. The suspensions were formulated with ZnO at a fixed concentration (5 wt%), sodium poly-(acrylate), as a viscosifier, and sodium dodecylsulfate (SDS), as a wetting agent. The rheological study shows that the suspensions exhibit a non-Newtonian, most often shear-thinning behavior and their apparent viscosity increases with polymer concentration. The rheogram...

  11. Small angle neutron scattering experiments on ''side-on fixed'' liquid crystal polyacrylates

    Energy Technology Data Exchange (ETDEWEB)

    Leroux, N. (Centre de Recherche Paul Pascal, Bordeaux-1 Univ., 33 - Pessac (France)); Keller, P. (Lab. Leon Brillouin, CEA-CNRS/CE Saclay, 91 - Gif-sur-Yvette (France)); Achard, M.F. (Centre de Recherche Paul Pascal, Bordeaux-1 Univ., 33 -Pessac (France)); Noirez, L. (Lab. Leon Brillouin, CEA-CNRS/CE Saclay, 91 -Gif-sur-Yvette (France)); Hardouin, F. (Centre de Recherche Paul Pascal, Bordeaux-1 Univ., 33 - Pessac (France))

    1993-08-01

    Small Angle Neutron Scattering experiments were carried out on liquid crystalline ''side-on fixed'' polyacrylates: we observe that the polymer backbone adopts a prolate conformation in the nematic phase. Such anisotropy of the global backbone is larger for smaller spacer lenght. In every case we measure at low temperatures a large chain extension as previously described in polysiloxanes. (orig.).

  12. Improvement in soil and sorghum health following the application of polyacrylate polymers to a Cd-contaminated soil

    Energy Technology Data Exchange (ETDEWEB)

    Guiwei, Q. [Department of Agricultural and Environmental Chemistry, Instituto Superior de Agronomia, Technical University of Lisbon (TULisbon), Tapada da Ajuda, 1349-017 Lisboa (Portugal); Soil and Environmental College, Shenyang Agricultural University, 110161 Shenyang, Liaoning Province (China); Varennes, A. de, E-mail: adevarennes@isa.utl.pt [Department of Agricultural and Environmental Chemistry, Instituto Superior de Agronomia, Technical University of Lisbon (TULisbon), Tapada da Ajuda, 1349-017 Lisboa (Portugal); Martins, L.L.; Mourato, M.P.; Cardoso, A.I. [Department of Agricultural and Environmental Chemistry, Instituto Superior de Agronomia, Technical University of Lisbon (TULisbon), Tapada da Ajuda, 1349-017 Lisboa (Portugal); Mota, A.M. [Department of Chemical Engineering, Instituto Superior Tecnico, Technical University of Lisbon (TULisbon), Av. Rovisco Pais, 1049-001 Lisboa (Portugal); Pinto, A.P. [Instituto de Ciencias Agrarias Mediterranicas (ICAM), University of Evora, R. Romao Ramalho no. 59, 7000 Evora (Portugal); Goncalves, M.L. [Department of Chemical Engineering, Instituto Superior Tecnico, Technical University of Lisbon (TULisbon), Av. Rovisco Pais, 1049-001 Lisboa (Portugal)

    2010-01-15

    Contamination of soils with cadmium (Cd) is a serious global issue due to its high mobility and toxicity. We investigated the application of insoluble polyacrylate polymers to improve soil and plant health. Sorghum was grown in a Cd-contaminated sandy soil. Polyacrylate polymers at 0.2% (w/w) were added to half of the soil. Control soil without plants was also included in the experiment. Growth of sorghum was stimulated in the polymer-amended soil. The concentration of Cd in the shoots, and the activities of catalase and ascorbate peroxidase decreased in plants from polymer-amended soil compared with unamended control. The amount of CaCl{sub 2}-extractable Cd in the polymer-amended soil was 55% of that in the unamended soil. The Cd extracted in sorghum shoots was 0.19 mg per plant grown on soil without polymer and 0.41 mg per plant grown on polymer-amended soil. The total amount of Cd removed from each pot corresponded to 1.5 and more than 6% of soil CaCl{sub 2}-extractable Cd in unamended and polymer-amended soil, respectively. The activities of soil acid phosphatase, {beta}-glucosidase, urease, protease and cellulase were greatest in polymer-amended soil with sorghum. In conclusion, the application of polyacrylate polymers to reduce the bioavailable Cd pool seems a promising method to enhance productivity and health of plants grown on Cd-contaminated soils.

  13. Carbonate minerals in porous media decrease mobility of polyacrylic acid modified zero-valent iron nanoparticles used for groundwater remediation

    International Nuclear Information System (INIS)

    The limited transport of nanoscale zero-valent iron (nZVI) in porous media is a major obstacle to its widespread application for in situ groundwater remediation. Previous studies on nZVI transport have mainly been carried out in quartz porous media. The effect of carbonate minerals, which often predominate in aquifers, has not been evaluated to date. This study assessed the influence of the carbonate minerals in porous media on the transport of polyacrylic acid modified nZVI (PAA-nZVI). Increasing the proportion of carbonate sand in the porous media resulted in less transport of PAA-nZVI. Predicted travel distances were reduced to a few centimeters in pure carbonate sand compared to approximately 1.6 m in quartz sand. Transport modeling showed that the attachment efficiency and deposition rate coefficient increased linearly with increasing proportion of carbonate sand. -- Highlights: •Mobility of nZVI NANOFER 25S was investigated in different saturated porous media. •nZVI transport in carbonate-containing porous media was elucidated and quantified. •Mobility of polyacrylic acid-coated nZVI significantly ceases in carbonate-containing media. •Deposition rate coefficient increases linearly with increasing carbonate content. -- Carbonate minerals in porous aquifers significantly decrease the mobility of commercially available polyacrylic acid modified nanoscale zero-valent iron

  14. Separation of poly(acrylic acid) salts according to topology using capillary electrophoresis in the critical conditions.

    Science.gov (United States)

    Maniego, Alison R; Ang, Dale; Guillaneuf, Yohann; Lefay, Catherine; Gigmes, Didier; Aldrich-Wright, Janice R; Gaborieau, Marianne; Castignolles, Patrice

    2013-11-01

    Branching was detected in polyacrylates synthesised through radical polymerization via solution-state NMR, while inconsistencies have been reported for the determination of the molar mass of hydrophilic polyacrylates using aqueous-phase and organic-phase size-exclusion chromatography. In this work, poly(sodium acrylate)s, PNaAs, of various topologies were separated for the first time using free-solution capillary electrophoresis (CE). Free-solution CE does not separate the PNaAs by their molar mass, similarly to separations by liquid chromatography in the critical conditions, rather by different topologies (linear, star branched, and hyperbranched). The electrophoretic mobility of PNaAs increases as the degree of branching decreases. Separation is shown to be not only by the topology but also by the end groups as expected for a separation in the critical conditions: replacing a relatively bulky nitroxide end group with hydrogen atom yielded a higher electrophoretic mobility. This novel method, capillary electrophoresis in the critical conditions enabled, for the first time, the separation of hydrophilic polyacrylates according to their topology (branching) and their chain ends. This will allow meaningful and accurate characterization of their branched topologies as well as molar masses and progress in for advanced applications such as drug delivery or flocculation. PMID:23732867

  15. Improvement in soil and sorghum health following the application of polyacrylate polymers to a Cd-contaminated soil

    International Nuclear Information System (INIS)

    Contamination of soils with cadmium (Cd) is a serious global issue due to its high mobility and toxicity. We investigated the application of insoluble polyacrylate polymers to improve soil and plant health. Sorghum was grown in a Cd-contaminated sandy soil. Polyacrylate polymers at 0.2% (w/w) were added to half of the soil. Control soil without plants was also included in the experiment. Growth of sorghum was stimulated in the polymer-amended soil. The concentration of Cd in the shoots, and the activities of catalase and ascorbate peroxidase decreased in plants from polymer-amended soil compared with unamended control. The amount of CaCl2-extractable Cd in the polymer-amended soil was 55% of that in the unamended soil. The Cd extracted in sorghum shoots was 0.19 mg per plant grown on soil without polymer and 0.41 mg per plant grown on polymer-amended soil. The total amount of Cd removed from each pot corresponded to 1.5 and more than 6% of soil CaCl2-extractable Cd in unamended and polymer-amended soil, respectively. The activities of soil acid phosphatase, β-glucosidase, urease, protease and cellulase were greatest in polymer-amended soil with sorghum. In conclusion, the application of polyacrylate polymers to reduce the bioavailable Cd pool seems a promising method to enhance productivity and health of plants grown on Cd-contaminated soils.

  16. The Modification of Sodium Polyacrylate Water Solution Cooling Properties by AL2O3

    Directory of Open Access Journals (Sweden)

    Wojciech Gęstwa

    2010-01-01

    Based on cooling curves, it can be concluded that for the water solution of sodium polyacrylate with AL2O3 nanoparticles in comparison to water and 10% polymer water solution lower cooling speed is obtained. The cooling medium containing nanoparticles provides lower cooling speed in the smallest surface austenite occurance (500–600 C in the charts of the CTP for most nonalloy structural steels and low-alloy steels. However lower cooling temperature at the beginning of martensitic transformation causes the formation of smaller internal stresses, leading to smaller dimensional changes and hardening deformation. For the quenching media the wetting angle was appointed by the drop-shape method. These studies showed the best wettability of polymer water solution (sodium polyacrylate with the addition of AL2O3 nanoparticles, whose wetting angle was about 65 degrees. Obtaining the smallest wetting angle for the medium containing nanoparticles suggests that the heat transfer to the cooling medium is larger. This allows slower cooling at the same time ensuring its homogeneity. The obtained values of wetting angle confirm the conclusions drawn on the basis of cooling curves and allowus to conclude that in the case of the heat transfer rate it will have a lower value than for water and 10% polymer water solution. In the research on hardened carburized steel samples C10 and 16MnCr5 surface hardness, impact strength and changes in the size of cracks in Navy C-ring sample are examined. On this basis of the obtained results it can be concluded that polymer water solution with nanoparticles allows to obtain a better impact strength at comparable hardness on the surface. Research on the dimensional changes on the basis of the sample of Navy C-ring also shows small dimensional changes for samples carburized and hardened in 10% polymer water solution with the addition of nanoparticles AL2O3. Smaller dimensional changes were obtained for samples of steel 16MnCr5 thanfar C10. The

  17. Effect of sodium polyacrylate molecular weight on the crystallogenesis of calcium carbonate

    Science.gov (United States)

    Jada, A.; Ait Akbour, R.; Jacquemet, C.; Suau, J. M.; Guerret, O.

    2007-08-01

    Aqueous solutions of sodium polyacrylates (NaPA) series having molecular weights ( Mw) ranging from 2540 to 9890 g mol -1 are used as precipitation media to control the size and shape of calcium carbonate (CaCO 3) particles. The retarding effect of polyacrylates on CaCO 3 nucleation is evidenced by the increase of the induction time, τ, of the precipitated CaCO 3, from τ=55 s in the absence of additives, to τ values in the range 100-2500 s in the presence of NaPA samples. The data also show the coexistence of two polymorphs, calcite and vaterite, for CaCO 3 particles as prepared in the presence of NaPA samples. The vaterite fraction, fv, varies in all instances with the polymer concentration, Cpoly (g. L -1), and reaches its maximum value, fv,max at optimal ratio, R (mol. g -1), of Ca ion to polymer (NaPA), R=[Ca]/([NaPA]=Cpoly). No simple general trend is found to explain the influence of the molecular weight ( Mw) of NaPA on the induction time, τ, and on the vaterite fraction, fv, since these two parameters are found to vary with Cpoly and Mw. However, under certain experimental conditions, an optimum polymer molecular weight ( Mw=5530 g mol -1) of the NaPA series, gives the highest values of fv,max and τ. Such optimum indicates the influence of Mw of NaPA on CaCO 3 nucleation and growth, and it is related to the surface density and the rate of adsorption of the polymer onto the growing crystal. The CaCO 3 particle size is reduced from about 20 μm, as obtained in the control experiment, to sizes varying in the range 2-8 μm in the presence NaPA samples. Polymers having low Mw values ( Mw<5000 g mol -1) are found to be more efficient in reducing the CaCO 3 particle size.

  18. A self-cleaning coating based on commercial grade polyacrylic latex modified by TiO{sub 2}/Ag-exchanged-zeolite-A nanocomposite

    Energy Technology Data Exchange (ETDEWEB)

    Nosrati, Rahimeh, E-mail: ra.nosrati@gmail.com [Polymer Composite Research Laboratory, Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz (Iran, Islamic Republic of); Olad, Ali, E-mail: a.olad@yahoo.com [Polymer Composite Research Laboratory, Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz (Iran, Islamic Republic of); Nofouzi, Katayoon, E-mail: nofouzi@tabrizu.ac.ir [Faculty of Veterinary Medicine, University of Tabriz, Tabriz (Iran, Islamic Republic of)

    2015-08-15

    Graphical abstract: - Highlights: • A novel nanocomposite coating based on polyacrylic was prepared. • Nanostructured TiO{sub 2}/Ag-exchanged-zeolite-A composite material was prepared. • Prepared nanocomposite used as additive for modification of polyacrylic latex. • Modified coatings show self-cleaning and antibacterial properties. • Modified coatings show better stability in water in versus of unmodified polymer. - Abstract: The commercial grade polyacrylic latex was modified in order to prepare a self-cleaning coating. TiO{sub 2}/Ag-exchanged-zeolite-A nanocomposite was prepared and used as additive in the matrix of polyacrylic latex to achieve a hydrophilic and photocatalytic coating. FTIR and UV–visible spectroscopy, X-ray diffraction patterns and FESEM were used to characterize the composition and structure of the nanocomposites and coatings. The acrylic coatings, were prepared by using of TiO{sub 2}/Ag-exchanged-zeolite-A additive, had better UV and visible light absorption, hydrophilic, degradation of organic pollutants, stability in water and antimicrobial properties than pristine commercial grade polyacrylic latex coating. According to the results, the modified polyacrylic based coating containing 0.5 wt% of TiO{sub 2}/Ag-exchanged-zeolite-A nanocomposite additive with TiO{sub 2} to Ag-exchanged-zeolite-A ratio of 1:2 was the best coating considering most of useful properties such as small band gap and low water contact angle. The water contact angle for unmodified polyacrylic latex coating was 68° which was decreased to less than 10° in modified coating after 24 h LED lamp illumination.

  19. A self-cleaning coating based on commercial grade polyacrylic latex modified by TiO2/Ag-exchanged-zeolite-A nanocomposite

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • A novel nanocomposite coating based on polyacrylic was prepared. • Nanostructured TiO2/Ag-exchanged-zeolite-A composite material was prepared. • Prepared nanocomposite used as additive for modification of polyacrylic latex. • Modified coatings show self-cleaning and antibacterial properties. • Modified coatings show better stability in water in versus of unmodified polymer. - Abstract: The commercial grade polyacrylic latex was modified in order to prepare a self-cleaning coating. TiO2/Ag-exchanged-zeolite-A nanocomposite was prepared and used as additive in the matrix of polyacrylic latex to achieve a hydrophilic and photocatalytic coating. FTIR and UV–visible spectroscopy, X-ray diffraction patterns and FESEM were used to characterize the composition and structure of the nanocomposites and coatings. The acrylic coatings, were prepared by using of TiO2/Ag-exchanged-zeolite-A additive, had better UV and visible light absorption, hydrophilic, degradation of organic pollutants, stability in water and antimicrobial properties than pristine commercial grade polyacrylic latex coating. According to the results, the modified polyacrylic based coating containing 0.5 wt% of TiO2/Ag-exchanged-zeolite-A nanocomposite additive with TiO2 to Ag-exchanged-zeolite-A ratio of 1:2 was the best coating considering most of useful properties such as small band gap and low water contact angle. The water contact angle for unmodified polyacrylic latex coating was 68° which was decreased to less than 10° in modified coating after 24 h LED lamp illumination

  20. Reversible switching in self-assembled monolayers of azobenzene thiolates on Au (111) probed by threshold photoemission

    International Nuclear Information System (INIS)

    Highlights: ► Photoelectron spectroscopy of liquid phase prepared SAMs of azobenzene derivative. ► Photo-induced reversible switching in densely packed SAM is monitored. ► Maximum density of switched molecules in SAM is derived from photoemission data. ► Switching reaction only enabled at defects sites within the molecular layer. - Abstract: The reversible photo- and thermally activated isomerization of the molecular switch 3-(4-(4-Hexyl-phenylazo)-phenoxy)-propane-1-thiol (ABT, short for AzoBenzeneThiol) deposited by self-assembly from solution on Au (111) was studied using laser-based photoelectron spectroscopy. Differences in the molecular dipole moment characteristic for the trans and the cis isomer of ABT were monitored via changes in the sample work function, accessible by detection of the threshold energy for photoemission. A quantitative analysis of our data shows that the fraction of molecules within the densely packed monolayer that undergoes a switching process is of the order of 1%. This result indicates the relevance of substrate and film defects required to overcome the steric or electronic hindrance of the isomerization reaction in a densely packed monolayer.

  1. Azobenzene-caged sulforhodamine dyes: a novel class of ‘turn-on’ reactive probes for hypoxic tumor cell imaging

    Science.gov (United States)

    Chevalier, Arnaud; Piao, Wen; Hanaoka, Kenjiro; Nagano, Tetsuo; Renard, Pierre-Yves; Romieu, Anthony

    2015-12-01

    New sulforhodamine-based fluorescent ‘turn-on’ probes have been developed for the direct imaging of cellular hypoxia. Rapid access to this novel class of water-soluble ‘azobenzene-caged’ fluorophores was made possible through an easily-implementable azo-coupling reaction between a fluorescent primary arylamine derived from a sulforhodamine 101 scaffold (named SR101-NaphtNH 2 ) and a tertiary aniline whose N-substituents are neutral, cationic, or zwitterionic. The detection mechanism is based on the bioreductive cleavage of the azo bond that restores strong far-red fluorescence (emission maximum at 625 nm) by regenerating the original sulforhodamine SR101-NaphtNH 2 . This valuable fluorogenic response was obtained for the three ‘smart’ probes studied in this work, as shown by an in vitro assay using rat liver microsomes placed under aerobic and then under hypoxic conditions. Most importantly, the probe namely SR101-NaphtNH 2 -Hyp-diMe was successfully applied for imaging the hypoxic status of tumor cells (A549 cells).

  2. Synthesis, optical and thermal behaviour of palladium(II) complexes with 4-(4-alkoxy-2-hydroxybenzylideneamino)azobenzene

    Indian Academy of Sciences (India)

    Boon-Teck Heng; Guan-Yeow Yeap; Daisuke Takeuchi

    2013-11-01

    A series of new Pd(II) complexes derived from the reaction of palladium acetate with 4-(4-alkoxy-2-hydroxybenzylideneamino)azobenzene having the flexible terminal chain of OCH2+1, in which n are even numbers ranging from 8 to 16, has been successfully synthesized. The physical measurement and spectroscopic techniques (FTIR and 1H-NMR) reveal that the Pd(II) complexes possess the Pd-N and Pd-O coordination modes in which the central Pd(II) adopts square-planar geometry. The observation under the polarized light shows that all the ligands and Pd(II) complexes exhibit enantiotropic mesophases. The ligands with -octyloxy and -decyloxy flexible chains exhibit the nematic (N) and smectic A (SmA) phases whilst the Pd(II) complexes show exclusive SmA phase. The SmA phase observed in Pd(II) complexes can be supported by the presence of focal conic fan-shaped texture with the presence of curved lines which are prominent during the cooling process. On the other hand, the comparison studies show that Pd(II) complexes possess exceptional higher phase transition temperatures as compared to the corresponding Cu(II) and Ni(II) complexes.

  3. Covalent functionalization of graphene by azobenzene with molecular hydrogen bonds for long-term solar thermal storage.

    Science.gov (United States)

    Feng, Yiyu; Liu, Hongpo; Luo, Wen; Liu, Enzuo; Zhao, Naiqin; Yoshino, Katsumi; Feng, Wei

    2013-01-01

    Reduced graphene oxide-azobenzene (RGO-AZO) hybrids were prepared via covalent functionalization for long-term solar thermal storage. Thermal barrier (ΔEa) of cis to tran reversion and thermal storage (ΔH) were improved by molecular hydrogen bonds (H-bonds) through ortho- or para-substitution of AZO. Intramolecular H-bonds thermally stabilized cis-ortho-AZO on RGO with a long-term half-life of 5400 h (ΔEa = 1.2 eV), which was much longer than that of RGO-para-AZO (116 h). RGO-para-AZO with one intermolecular H-bond showed a high density of thermal storage up to 269.8 kJ kg(-1) compared with RGO-ortho-AZO (149.6 kJ kg(-1)) with multiple intra- and intermolecular H-bonds of AZO according to relaxed stable structures. Thermal storage in experiment was the same order magnitude to theoretical data based on ΔH calculated by density functional theory and packing density. Photoactive RGO-AZO hybrid can be developed for high-performance solar thermal storage by optimizing molecular H-bonds. PMID:24247355

  4. Molecular structure and vibrational and chemical shift assignments of 3‧-chloro-4-dimethylamino azobenzene by DFT calculations

    Science.gov (United States)

    Toy, Mehmet; Tanak, Hasan

    2016-01-01

    In the present work, a combined experimental and theoretical study on ground state molecular structure, spectroscopic and nonlinear optical properties of azo compound 3‧-chloro-4-dimethlamino azobenzene are reported. The molecular geometry, vibrational wavenumbers and the first order hyperpolarizability of the title compound were calculated with the help of density functional theory computations. The optimized geometric parameters obtained by using DFT (B3LYP/6-311++G(d,p)) show good agreement with the experimental data. The vibrational transitions were identified based on the recorded FT-IR spectra in the range of 4000-400 cm-1 for solid state. The 1H isotropic chemical shifts with respect to TMS were also calculated using the gauge independent atomic orbital (GIAO) method and compared with the experimental data. Using the TD-DFT method, electronic absorption spectra of the title compound have been predicted, and good agreement is determined with the experimental ones. To investigate the NLO properties of the title compound, the polarizability and the first hyperpolarizability were calculated using the density functional B3LYP method with the 6-311++G(d,p) basis set. According to results, the title compound exhibits non-zero first hyperpolarizability value revealing second order NLO behavior. In addition, DFT calculations of the title compound, molecular electrostatic potential and frontier molecular orbitals were also performed at 6-311++G(d,p) level of theory.

  5. In situ investigations on the preparations of layer-by-layer films containing azobenzene and applications for LC display devices

    International Nuclear Information System (INIS)

    Preparations of alternate layer-by-layer self-assembled films of poly(diallyldimethyl ammonium chloride) (PDADMAC) and Direct Red 80 (DR80, azobenzene dye) and photo-induced surface relief gratings (SRGs) of the films have been investigated in situ using attenuated total reflection (ATR), that is, surface plasmon resonance spectroscopy (SPS) and quartz crystal microbalance (QCM) measurements. Gratings of the PDADMAC/DR80 films were fabricated by exposure to interference patterns of Ar+ laser light at 488 nm for 30 min. The formation of the gratings was observed using atomic force microscopy (AFM). The films were used for applications to liquid crystal (LC) display devices, and aligning properties of nematic liquid crystal molecules, 5CB, on the SRG in the films were also investigated in a hybrid LC cell configuration by monitoring birefringence properties of the LC cell in situ. It was estimated that the LC molecules in the cell did not align immediately after the photo-induced SRG was inscribed, but almost along the gratings after heat treatment at 40 deg. C for 1 min

  6. Nanocomposites of Polyacrylic Acid Nanogels and Biodegradable Polyhydroxybutyrate for Bone Regeneration and Drug Delivery

    Directory of Open Access Journals (Sweden)

    Mikael Larsson

    2014-01-01

    Full Text Available Biodegradable cell scaffolds and local drug delivery to stimulate cell response are currently receiving much scientific attention. Here we present a nanocomposite that combines biodegradation with controlled release of lithium, which is known to enhance bone growth. Nanogels of lithium neutralized polyacrylic acid were synthesized by microemulsion-templated polymerization and were incorporated into a biodegradable polyhydroxybutyrate (PHB matrix. Nanogel size was characterized using dynamic light scattering, and the nanocomposites were characterized with regard to structure using scanning electron microscopy, mechanical properties using tensile testing, permeability using tritiated water, and lithium release in PBS using a lithium specific electrode. The nanogels were well dispersed in the composites and the mechanical properties were good, with a decrease in elastic modulus being compensated by increased tolerance to strain in the wet state. Approximately half of the lithium was released over about three hours, with the remaining fraction being trapped in the PHB for subsequent slow release during biodegradation. The prepared nanocomposites seem promising for use as dual functional scaffolds for bone regeneration. Here lithium ions were chosen as model drug, but the nanogels could potentially act as carriers for larger and more complex drugs, possibly while still carrying lithium.

  7. Conjugation, characterization and toxicity of lipophosphoglycan-polyacrylic acid conjugate for vaccination against leishmaniasis.

    Science.gov (United States)

    Topuzogullari, Murat; Cakir Koc, Rabia; Dincer Isoglu, Sevil; Bagirova, Melahat; Akdeste, Zeynep; Elcicek, Serhat; Oztel, Olga N; Yesilkir Baydar, Serap; Canim Ates, Sezen; Allahverdiyev, Adil M

    2013-01-01

    Research on the conjugates of synthetic polyelectrolytes with antigenic molecules, such as proteins, peptides, or carbohydrates, is an attractive area due to their highly immunogenic character in comparison to classical adjuvants. For example, polyacrylic acid (PAA) is a weak polyelectrolyte and has been used in several biomedical applications such as immunological studies, drug delivery, and enzyme immobilization. However, to our knowledge, there are no studies that document immune-stimulant properties of PAA in Leishmania infection. Therefore, we aimed to develop a potential vaccine candidate against leishmaniasis by covalently conjugating PAA with an immunologically vital molecule of lipophosphoglycan (LPG) found in Leishmania parasites. In the study, LPG and PAA were conjugated by a multi-step procedure, and final products were analyzed with GPC and MALDI-TOF MS techniques. In cytotoxicity experiments, LPG-PAA conjugates did not indicate toxic effects on L929 and J774 murine macrophage cells. We assume that LPG-PAA conjugate can be a potential vaccine candidate, and will be immunologically characterized in further studies to prove its potential. PMID:23731716

  8. Cellulose nanocrystal-filled poly(acrylic acid) nanocomposite fibrous membranes

    Science.gov (United States)

    Lu, Ping; Hsieh, You-Lo

    2009-10-01

    Nanocomposite fibrous membranes have been fabricated by electrospinning cellulose nanocrystal (CNC)-loaded poly(acrylic acid) (PAA) ethanol mixtures. Incorporating CNC in PAA significantly reduced fiber diameters and improved fiber uniformity. The average diameters of the as-spun nanocomposite fibers were significantly reduced from 349 nm to 162 nm, 141 nm, 90 nm and 69 nm at 5%, 10%, 15% and 20% CNC loading (by weight of a constant 4% PAA solution), respectively. CNC was well dispersed in the fibers as isolated rods oriented along the fiber axis and as spheres in the PAA matrix. The Young modulus and stress of the PAA/CNC nanocomposite fibers were significantly improved with increasing CNC loadings by up to 35-fold and 16-fold, respectively. Heat-induced esterification between the CNC surface hydroxyls and PAA carboxyl groups produced covalent crosslinks at the CNC-PAA interfaces, rendering the nanocomposite fibrous membranes insoluble in water, more thermally stable and far more superior in tensile strength. With 20% CNC, the crosslinked nanocomposite fibrous membrane exhibited a very impressive 77-fold increase in modulus and 58-fold increase in stress.

  9. Cellulose nanocrystal-filled poly(acrylic acid) nanocomposite fibrous membranes

    International Nuclear Information System (INIS)

    Nanocomposite fibrous membranes have been fabricated by electrospinning cellulose nanocrystal (CNC)-loaded poly(acrylic acid) (PAA) ethanol mixtures. Incorporating CNC in PAA significantly reduced fiber diameters and improved fiber uniformity. The average diameters of the as-spun nanocomposite fibers were significantly reduced from 349 nm to 162 nm, 141 nm, 90 nm and 69 nm at 5%, 10%, 15% and 20% CNC loading (by weight of a constant 4% PAA solution), respectively. CNC was well dispersed in the fibers as isolated rods oriented along the fiber axis and as spheres in the PAA matrix. The Young modulus and stress of the PAA/CNC nanocomposite fibers were significantly improved with increasing CNC loadings by up to 35-fold and 16-fold, respectively. Heat-induced esterification between the CNC surface hydroxyls and PAA carboxyl groups produced covalent crosslinks at the CNC-PAA interfaces, rendering the nanocomposite fibrous membranes insoluble in water, more thermally stable and far more superior in tensile strength. With 20% CNC, the crosslinked nanocomposite fibrous membrane exhibited a very impressive 77-fold increase in modulus and 58-fold increase in stress.

  10. Direct Synthesis of Hyperbranched Poly(acrylic acid-co-3-hydroxypropionate

    Directory of Open Access Journals (Sweden)

    Efkan Çatıker

    2015-01-01

    Full Text Available Hyperbranched poly(acrylic acid-co-3-hydroxypropionate (PAcHP was synthesized by base-catalyzed hydrogen transfer polymerization of acrylic acid through one step. The copolymers obtained through solution and bulk polymerization were insoluble in water and all organic solvents tried. Structural and compositional characterizations of hyperbranched PAcHP were performed by using FTIR, solid 13C-NMR, TGA, and titrimetric analysis. Acrylate fraction of the hyperbranched PAcHP obtained via bulk polymerization was determined as 60–65% by comparing TGA curves of hyperbranched PAcHP and pure poly(3-hydroxy propionate (PHP. However, analytical titration of the same sample revealed that acrylic acid units were about 47.3%. The results obtained from TGA and analytical titration were used to evaluate the chemical structure of the copolymer. Hyperbranched PAcHP exhibited hydrogel properties. Swelling behavior of the copolymer was investigated at a wide pH range and ionic strength. The dynamic swelling profiles of hyperbranched PAcHP exhibited a fast swelling behavior in the first hour and achieved the equilibrium state within 12 h in PBS. Depending on the conditions, the copolymers exhibited swelling ratios up to 2100%. As the copolymer has easily biodegradable propionate and versatile functional acrylic acid units, it can be used as not only biodegradable material in medical applications but also raw material in personal care commodities.

  11. Interaction of polyacrylates with porcine pepsin and the gastric mucus barrier: a mechanism for mucosal protection.

    Science.gov (United States)

    Foster, S N; Pearson, J P; Hutton, D A; Allen, A; Dettmar, P W

    1994-12-01

    1. The mechanism of interaction of the polyacrylates, carbopols with the mucus barrier in vivo has been investigated in vitro. 2. Carbopol caused a dramatic increase in the viscosity of porcine gastric mucin solutions that was up to 19-fold greater than that of the sum of the individual polymers. 3. The mucin-carbopol interaction was stable after an initial 30 min period for up to 36 h at 25 degrees C or 37 degrees C. It was reduced by increasing the temperature from 20 degrees C to 45 degrees C, was unaffected by pH and ionic strength, but was enhanced by Ca2+. 4. The magnitude of the interaction between mucin and carbopol depended on the polymeric structure of the mucin and the molecular size and level of cross-linking of the carbopol. 5. The interactions were reversible and increased with increasing carbopol and mucin concentration. The dramatic increase in viscosity can be explained in terms of space filling by the mucin molecules leading to predominantly carbopol-carbopol interactions. 6. Carbopol 934P inhibits pepsin hydrolysis and therefore has potential as a mucosal protective agent in vivo. PMID:7874865

  12. A theory-based approach to thermal field-flow fractionation of polyacrylates.

    Science.gov (United States)

    Runyon, J Ray; Williams, S Kim Ratanathanawongs

    2011-09-28

    A theory-based approach is presented for the development of thermal field-flow fractionation (ThFFF) of polyacrylates. The use of ThFFF for polymer analysis has been limited by an incomplete understanding of the thermal diffusion which plays an important role in retention and separation. Hence, a tedious trial-and-error approach to method development has been the normal practice when analyzing new materials. In this work, thermal diffusion theories based on temperature dependent osmotic pressure gradient and polymer-solvent interaction parameters were used to estimate thermal diffusion coefficients (D(T)) and retention times (t(r)) for different polymer-solvent pairs. These calculations identified methyl ethyl ketone as a solvent that would cause significant retention of poly(n-butyl acrylate) (PBA) and poly(methyl acrylate) (PMA). Experiments confirmed retention of these two polymers that have not been previously analyzed by ThFFF. Theoretical and experimental D(T)s and t(r)s for PBA, PMA, and polystyrene in different solvents agreed to within 20% and demonstrate the feasibility of this theory-based approach. PMID:21872869

  13. PREPARATION AND PROPERTIES OF ETHYL-CYANOETHYL CELLULOSE/POLYACRYLIC ACID COMPOSITE FILMS WITH REFLECTION COLORS

    Institute of Scientific and Technical Information of China (English)

    Yong Huang

    2001-01-01

    Ethyl-cyanoethyl cellulose [(E-CE)C]/acrylic acid (AA) becomes a cholesteric liquid crystalline solution with vivid colors when the (E-CE)C concentration is 42 wt% ~52 wt%. (E-CE)C/polyacrylic acid (PAA) composites with cholesteric structure were prepared by polymerizing AA in (E-CE)C/AA liquid crystalline solutions. The layers of ordered polymer chains in the cholesteric phase were inclined during polymerization and the degree of the inclination depended on the polymerization temperature and the concentration of the solution before polymerization. The cholesteric structure in the composites could not be changed when temperature was lower than 100C. Cross-linking of the PAA in composites improved their water-resistance. The cholesteric order of the composites without cross-linking was destroyed when they where immersed in water. The color derived from the selective reflection of the cholesteric phase of the cross-linked composites turned from blue to red after the composites absorbed water. The color of the composites could be returned to the original one when the absorbed water was removed from the swollen composites.

  14. Large area UV casting using diverse polyacrylates of microchannels separated by high aspect ratio microwalls.

    Science.gov (United States)

    Zhou, W X; Chan-Park, Mary B

    2005-05-01

    Large area molding of long and deep microchannels separated by high aspect ratio microwalls is important for high sensitivity and high throughput microfluidic devices. Ultraviolet (UV) casting is a feasible, economical and convenient method of replication of such microstructures in plastics. It is shown that a wide variety of polyacrylates with diverse properties such as those made from epoxy (EP), polyurethane (UR), polyester (ES), poly (ethylene glycol) (EG) and poly(propylene glycol) (PG) can be used for the high aspect ratio (7-9) UV casting of such linear microstructures over a 100 mm diameter, enlarging the range of applications of the replicated microstructures. Some challenges arise. With the EG formulation, wavy microstructures were observed; this can be overcome by stress relaxation. With non-polar PG formulation, poor adhesion between the polyester substrate and resin can lead to delamination of the casting from the substrate during demolding; this can be overcome by pre-coating a partially cured same resin on the polyester substrate. An optimum UV irradiation time was important for cure at the deepest end of the microstructure without excessive crosslinking leading to much increased demolding forces. The viscosity and wetting capability of the formulations were found to affect replication fidelity. PMID:15856087

  15. Preparation and Properties of Moisture-absorbing Film Impregnated with Polyacrylic Acid Partial Sodium Salt Material

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Youn Suk; Park, Insik [Yonsei University, Wonju (Korea, Republic of); Choi, Hong Yeol [CJ Cheiljedang, Seoul (Korea, Republic of)

    2014-08-15

    Moisture is a major factor causing the deteriorative physical change, microbial growth, and chemical reaction of the products. In this study, the moisture absorbing composite films have been prepared with moisture absorbing material of polyacrylic acid partial sodium salt (PAPSS) impregnated on LLDPE polymer for the functional packaging applications. The results showed that PAPSS impregnated film illustrated uniformly dispersed PAPSS particles in the LLDPE polymer matrix. The transparency of the PAPSS impregnated film decreased slightly at higher PAPSS concentrations. An increase in the PAPSS content for moisture-absorbing films showed a similar decrease in tensile strength, percent elongation at break, and tear strength. Their values of films impregnated with PAPSS of 0.5, 1, and 2% showed no significant difference. Meanwhile, 4% PAPSS films significantly decreased the values of mechanical properties compared to the films impregnated with different PAPSS levels. Values of the oxygen permeability and water vapor permeability for PAPSS impregnated films decreased significantly with greater PAPSS. The results indicate that 4% PAPSS impregnated in LLDPE films had high affinity of moisture absorbencies compared to the other films. The mathematical equation that best described the moisture sorption isotherm of each film sample was the GAB equation at 25 .deg. C. The crystallization and melting temperatures of PAPSS films were influenced by the addition of PAPSS material, but showed good thermal stability.

  16. Characterization of bioactive RGD peptide immobilized onto poly(acrylic acid) thin films by plasma polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Seo, Hyun Suk; Ko, Yeong Mu; Shim, Jae Won [Department of Dental Materials, School of Dentistry, MRC Center, Chosun University, Gwangju (Korea, Republic of); Lim, Yun Kyong; Kook, Joong-Ki [Department of Oral Biochemistry, School of Dentistry, Chosun University, Gwangju (Korea, Republic of); Cho, Dong-Lyun [School of Applied Chemical Engineering and Center for Functional Nano Fine Chemicals, Chonnam National University, Gwangju (Korea, Republic of); Kim, Byung Hoon, E-mail: kim5055@chosun.ac.kr [Department of Dental Materials, School of Dentistry, MRC Center, Chosun University, Gwangju (Korea, Republic of)

    2010-11-01

    Plasma surface modification can be used to improve the surface properties of commercial pure Ti by creating functional groups to produce bioactive materials with different surface topography. In this study, a titanium surface was modified with acrylic acid (AA) using a plasma treatment and immobilized with bioactive arginine-glycine-aspartic acid (RGD) peptide, which may accelerate the tissue integration of bone implants. Both terminals containing the -NH{sub 2} of RGD peptide sequence and -COOH of poly(acrylic acid) (PAA) thin film were combined with a covalent bond in the presence of 1-ethyl-3-3-dimethylaminopropyl carbodiimide (EDC). The chemical structure and morphology of AA film and RGD immobilized surface were investigated by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT-IR), atomic force microscopy (AFM), and scanning electron microscopy (SEM). All chemical analysis showed full coverage of the Ti substrate with the PAA thin film containing COOH groups and the RGD peptide. The MC3T3-E1 cells were cultured on each specimen, and the cell alkaline phosphatase (ALP) activity were examined. The surface-immobilized RGD peptide has a significantly increased the ALP activity of MC3T3-E1 cells. These results suggest that the RGD peptide immobilization on the titanium surface has an effect on osteoblastic differentiation of MC3T3-E1 cells and potential use in osteo-conductive bone implants.

  17. Characterization of bioactive RGD peptide immobilized onto poly(acrylic acid) thin films by plasma polymerization

    International Nuclear Information System (INIS)

    Plasma surface modification can be used to improve the surface properties of commercial pure Ti by creating functional groups to produce bioactive materials with different surface topography. In this study, a titanium surface was modified with acrylic acid (AA) using a plasma treatment and immobilized with bioactive arginine-glycine-aspartic acid (RGD) peptide, which may accelerate the tissue integration of bone implants. Both terminals containing the -NH2 of RGD peptide sequence and -COOH of poly(acrylic acid) (PAA) thin film were combined with a covalent bond in the presence of 1-ethyl-3-3-dimethylaminopropyl carbodiimide (EDC). The chemical structure and morphology of AA film and RGD immobilized surface were investigated by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT-IR), atomic force microscopy (AFM), and scanning electron microscopy (SEM). All chemical analysis showed full coverage of the Ti substrate with the PAA thin film containing COOH groups and the RGD peptide. The MC3T3-E1 cells were cultured on each specimen, and the cell alkaline phosphatase (ALP) activity were examined. The surface-immobilized RGD peptide has a significantly increased the ALP activity of MC3T3-E1 cells. These results suggest that the RGD peptide immobilization on the titanium surface has an effect on osteoblastic differentiation of MC3T3-E1 cells and potential use in osteo-conductive bone implants.

  18. Preparation and characterization of aqueous polyurethane oil/polyacrylate latex interpenetrating polymer network

    Science.gov (United States)

    Zhou, M. M.; Ma, L. L.; Du, J.; Cao, F.; Xiao, J. J.

    2015-07-01

    A series of aqueous polyurethane oil (network I)/polyacrylate (network II) latex interpenetrating polymer networks (LIPNs) were synthesized via the technology of latex interpenetrating polymer network combined seed emulsion polymerization process. Fourier transform infrared (FTIR) spectroscopy, laser particle size distributing analyzer and universal tension machine were utilized to characterize the bulk structures and mechanical properties of LIPNs. For used as damping material, the damping performance of LIPNs were analyzed by dynamic mechanical analysis (DMA). It was found that the damping temperature region of LIPN was wider than those of aqueous polyurethane oil, the temperature region with greater tanδ changed with the TPGDA content and hard-/soft-segment mass weight ratio (mMMA/mBA) and the glass transition temperature (Tg) of the network I and network II in LIPN occurred within shift each other, even overlap with increasing mMMA/mBA value. The results show that LIPNs synthesized through the combined process have greater tanδ and wider damping temperature region, which is suitable for the use of damping coatings.

  19. pH-Responsive Behavior of Poly(acrylic acid) Brushes of Varying Thickness

    Science.gov (United States)

    Yadav, Vivek; Robertson, Megan; Conrad, Jacinta

    2015-03-01

    We have investigated the pH-dependent response of polyelectrolyte brushes of varying thickness. Our model system consists of poly(acrylic acid) brushes, which change from hydrophobic and neutral at low pH to hydrophilic and negatively charged at high pH, synthesized using a grafting-from approach at constant grafting density. As the polymer brush thickness increased, the brushes exhibited greater hysteresis in static water contact angle as a function of pH. We extracted the pKa of the polymer brushes from contact angle measurements. The relationship between the pKa and brush thickness depended on the order in which the brushes were exposed to solutions of varying pH: pKa decreased on increasing brush thickness when going from basic to acidic medium whereas pKa increased on increasing brush thickness when going from acidic to basic medium. We speculate that the origin of hysteresis can be explained by pH-dependent conformational changes in these polyelectrolyte brushes.

  20. Biodegradation of New Polymer Foundry Binders for the Example of the Composition Polyacrylic Acid/Starch

    Directory of Open Access Journals (Sweden)

    Beata Grabowska

    2011-04-01

    Full Text Available The investigations on the biodegradation process pathway of the new polymer binders for the example of water soluble compositionpolyacrylic acid/starch are presented in the hereby paper. Degradation was carried out in water environment and in a soil. Thedetermination of the total oxidation biodegradation in water environment was performed under laboratory conditions in accordance with the static water test system (Zahn-Wellens method, in which the mixture undergoing biodecomposition contained inorganic nutrient,activated sludge and the polymer composition, as the only carbon and energy source. The biodecomposition progress of the polymercomposition sample in water environment was estimated on the basis of the chemical oxygen demand (COD measurements and thedetermination the biodegradation degree, Rt, during the test. These investigations indicated that the composition polyacrylic acid/starchconstitutes the fully biodegradable material in water environment. The biodegradation degree Rt determined in the last 29th day of the test duration achieved 65%, which means that the investigated polymer composition can be considered to be fully biodegradable.During the 6 months biodegradation process of the cross-linked sample of the polymer composition in a garden soil several analysis ofsurface and structural changes, resulting from the sample decomposition, were performed. Those were: thermal analyses (TG-DSC,structural analyses (Raman spectroscopy and microscopic analyses (optical microscopy, AFM.

  1. Synthesis and characterization of zinc chloride containing poly(acrylic acid) hydrogel by gamma irradiation

    International Nuclear Information System (INIS)

    In this study, the characterization of zinc chloride incorporated into a poly(acrylic acid) (PAAc) hydrogel prepared by gamma-ray irradiation was investigated. Zinc chloride powder with different concentrations was dissolved in the PAAc solution, and it was crosslinked with gamma-ray irradiation. The effects of various parameters such as zinc ion concentration and irradiation doses on characteristics of the hydrogel formed were investigated in detail for obtaining an antibacterial wound dressing. In addition, the gel content, pH-sensitive (pH 4 or 7) swelling ratio, and UV–vis absorption spectra of the zinc particles in the hydrogels were characterized. Moreover, antibacterial properties of these new materials against Staphylococcus aureus and Escherichia coli strains were observed on solid growth media. The antibacterial tests indicated that the zinc chloride containing PAAc hydrogels have good antibacterial activity. - Highlights: • The characterization of zinc chloride containing PAA hydrogel was investigated. • The gel content increased with an increase in absorbed dose up to 75 kGy. • Finally, the zinc chloride based hydrogels have an antibacterial activity

  2. Inhibited growth of Pseudomonas aeruginosa by dextran- and polyacrylic acid-coated ceria nanoparticles

    Directory of Open Access Journals (Sweden)

    Wang Q

    2013-08-01

    Full Text Available Qi Wang,1 J Manuel Perez,2 Thomas J Webster1,3 1Bioengineering Program, College of Engineering, Northeastern University, Boston, MA, USA; 2Nanoscience Technology Center, University of Central Florida, Orlando, FL, USA; 3Department of Chemical Engineering, College of Engineering, Northeastern University, Boston, MA, USA Abstract: Ceria (CeO2 nanoparticles have been widely studied for numerous applications, but only a few recent studies have investigated their potential applications in medicine. Moreover, there have been almost no studies focusing on their possible antibacterial properties, despite the fact that such nanoparticles may reduce reactive oxygen species. In this study, we coated CeO2 nanoparticles with dextran or polyacrylic acid (PAA because of their enhanced biocompatibility properties, minimized toxicity, and reduced clearance by the immune system. For the first time, the coated CeO2 nanoparticles were tested in bacterial assays involving Pseudomonas aeruginosa, one of the most significant bacteria responsible for infecting numerous medical devices. The results showed that CeO2 nanoparticles with either coating significantly inhibited the growth of Pseudomonas aeruginosa, by up to 55.14%, after 24 hours compared with controls (no particles. The inhibition of bacterial growth was concentration dependent. In summary, this study revealed, for the first time, that the characterized dextran- and PAA-coated CeO2 nanoparticles could be potential novel materials for numerous antibacterial applications. Keywords: antibacterial, biomedical applications

  3. Preparation and properties of poly(acrylic acid) oligomer stabilized superparamagnetic ferrofluid.

    Science.gov (United States)

    Lin, Chia-Lung; Lee, Chia-Fen; Chiu, Wen-Yen

    2005-11-15

    Ferrofluids, which are stable dispersions of magnetic particles, behave as liquids that have strong magnetic properties. Nanoparticles of magnetite with a mean diameter of 10-15 nm, which are in the range of superparamagnetism, are usually prepared by the traditional method of co-precipitation from ferrous and ferric electrolyte solution. When diluted, the ferrofluid dispersions are not stable if anionic or cationic surfactants are used as the stabilizer. This work presents an efficient way to prepare a stable aqueous nanomagnetite dispersion. A stable ferrofluid containing Fe3O4 nanoparticles was synthesized via co-precipitation in the presence of poly(acrylic acid) oligomer. The mechanism, microstructure, and properties of the ferrofluid were investigated. The results indicate that the PAA oligomers promoted the nucleation and inhibited the growth of the magnetic iron oxide, and the average diameter of each individual Fe3O4 particle was smaller than 10 nm. In addition, the PAA oligomers provided both electrostatic and steric repulsion against particle aggregation, and the stability of dispersions could be controlled by adjusting the pH value of solution. A small amount of Fe2O3 was found in the nanoparticles but the superparamagnetic behavior of the nanoparticles was not affected. PMID:16009367

  4. SOYBEAN MEAL-BASED WOOD ADHESIVES ENHANCED BY MODIFIED POLYACRYLIC ACID SOLUTION

    Directory of Open Access Journals (Sweden)

    Qiang Gao,

    2012-01-01

    Full Text Available The effects of using sodium dodecyl sulfate (SDS and a modified polyacrylic acid solution (MPA on a soybean meal adhesive were investigated. Three-ply plywood specimens were fabricated to measure the water resistance of the adhesive (three-cycle soak test. The viscosity and solid content of the adhesive were measured. The cross-section and functional groups of the cured adhesive were evaluated using scanning electron microscope (SEM and Fourier transform infrared (FTIR spectroscopy, respectively. The results showed that using SDS improved the water resistance of the soybean meal adhesive by 30%. After incorporating MPA, the water resistance of the soybean meal/SDS/MPA adhesive was further improved by 60%, the viscosity of the adhesive was reduced by 81%, and the solid content of the adhesive increased by 15%. The plywood bonded by the soybean meal/SDS/MPA adhesive met the interior plywood requirements. SEM results showed no holes and cracks on the cross-section of the cured soybean meal/SDS/ MPA adhesive. FTIR analysis indicated that more peptide linkages were formed in the cured adhesive as MPA was incorporated.

  5. Characterization of bioactive RGD peptide immobilized onto poly(acrylic acid) thin films by plasma polymerization

    Science.gov (United States)

    Seo, Hyun Suk; Ko, Yeong Mu; Shim, Jae Won; Lim, Yun Kyong; Kook, Joong-Ki; Cho, Dong-Lyun; Kim, Byung Hoon

    2010-11-01

    Plasma surface modification can be used to improve the surface properties of commercial pure Ti by creating functional groups to produce bioactive materials with different surface topography. In this study, a titanium surface was modified with acrylic acid (AA) using a plasma treatment and immobilized with bioactive arginine-glycine-aspartic acid (RGD) peptide, which may accelerate the tissue integration of bone implants. Both terminals containing the -NH2 of RGD peptide sequence and -COOH of poly(acrylic acid) (PAA) thin film were combined with a covalent bond in the presence of 1-ethyl-3-3-dimethylaminopropyl carbodiimide (EDC). The chemical structure and morphology of AA film and RGD immobilized surface were investigated by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT-IR), atomic force microscopy (AFM), and scanning electron microscopy (SEM). All chemical analysis showed full coverage of the Ti substrate with the PAA thin film containing COOH groups and the RGD peptide. The MC3T3-E1 cells were cultured on each specimen, and the cell alkaline phosphatase (ALP) activity were examined. The surface-immobilized RGD peptide has a significantly increased the ALP activity of MC3T3-E1 cells. These results suggest that the RGD peptide immobilization on the titanium surface has an effect on osteoblastic differentiation of MC3T3-E1 cells and potential use in osteo-conductive bone implants.

  6. Graphene sheets stacked polyacrylate latex composites for ultra-efficient electromagnetic shielding

    Science.gov (United States)

    Li, Yong; Zhang, Song; Ni, Yuwei

    2016-07-01

    Graphene sheets (GS) are at the forefront of electromagnetic interference (EMI) shielding/attenuation materials science research because of their excellent electrical properties (Wen B et al 2014 Adv. Mater. 26 3484, Zhang Y et al 2015 Adv. Mater. 27 2049). GS/polyacrylate (PA) composites were prepared using a solvent-free latex technology, which favored the build-up of a segregated GS architecture stacked in the polymer matrix. GS were obtained from graphite flakes (GF) via a mechanical delamination approach in water. The microstructure, electrical, dielectric and electromagnetic shielding properties of the GS/PA composites were correlated in this manuscript. A remarkably low percolation threshold of ∼0.11 mass per cent for room-temperature electrical conductivity was obtained in the GS/PA composites owing to the stacked architecture of GS with high aspect ratios. This unique nanostructured GS architecture not only enhanced the electrical conductivity of composites, but also dramatically increased complex permittivity by inducing strong Maxwell–Wagner–Sillars (MWS) polarization at the highly conductive GS/non-conductive PA interfaces. The EMI shielding effectiveness (SE) of these composites was enhanced with increasing GS content, and the composite with 6 wt% GS loading exhibited a high EMI SE of ∼66 dB over a frequency of 8.2–12.4 GHz, resulting from the pronounced conduction loss, dielectric relaxation, and multi-scattering.

  7. Simulated sugar factory wastewater remediation kinetics using algal-bacterial raceway reactor promoted by polyacrylate polyalcohol.

    Science.gov (United States)

    Memon, Abdul Rehman; Andresen, John; Habib, Muddasar; Jaffar, Muhammad

    2014-04-01

    The remediation kinetics of simulated sugar factory wastewater (SFW) using an algal-bacterial culture (ABC) of Chlorella vulgaris in association with Pseudomonas putida in a raceway reactor was found to be enhanced by 89% with the addition of 80ppm of copolymer Polyacrylate polyalcohol (PAPA). This was achieved by efficient suspension of the ABC throughout the water body maintaining optimum pH and dissolved oxygen that led to rapid COD removal and improved algal biomass production. The suspension of the ABC using the co-polymer PAPA maintained a DO of 8-10mgl(-1) compared to 2-3mgl(-1) when not suspended. As a result, the non-suspended ABC only achieved a 50% reduction in COD after 96h compared to a 89% COD removal using 80ppm PAPA suspension. In addition, the algae biomass increased from 0.4gl(-1)d(-1) for the non-suspended ABC to 1.1gl(-1)d(-1) when suspended using 80ppm PAPA. PMID:24530948

  8. Protein absorption and fouling on poly(acrylic acid)-graft-polypropylene microfiltration membrane

    Science.gov (United States)

    Liu, Yanjun; Ma, Huiying; Lv, Chunying; Yang, Jia; Fu, Xueqi

    2009-07-01

    A series of pH-sensitive poly (acrylic acid)-graft-polypropylene hollow fiber microfiltration membranes were prepared by UV-photo-irradiation. Bovine serum albumin (BSA) was chosen as the model protein to investigate its absorption and fouling behaviors on membranes. The results showed that the hydrophilicity of grafted membrane was improved by poly(acrylic acid) chains with parts of membrane pores blocked. The grafted membranes were markedly pH-dependent on the water permeability as pH was altered from 1 to 11. The zeta potential of grafted membranes calculated by streaming potential was negative in most pH range. Electrostatic interaction energy calculated by DLVO theory showed the electric interaction force between grafted membrane and BSA was attractive. With the rise of grafting degree, the electric attractive force between grafted membrane and BSA increased as pH=3 and decreased as pH=8, while it kept basically unchanged as pH=4.7. As a result, most serious fouling was observed as pH=4.7. Grafted membranes had a lower BSA absorption and better antifouling behavior as pH=8, while the opposite result was revealed as pH=3. In conclusion, the absorption and fouling behavior of BSA on membranes was pH-dependent due to the pH-dependence of membrane charge, and the conformation of BSA and grafting chains.

  9. Effect of salt and surfactant concentration on the structure of polyacrylate gel/surfactant complexes.

    Science.gov (United States)

    Nilsson, Peter; Unga, Johan; Hansson, Per

    2007-09-20

    Small-angle X-ray scattering was used to elucidate the structure of crosslinked polyacrylate gel/dodecyltrimethylammonium bromide complexes equilibrated in solutions of varying concentrations of surfactant and sodium bromide (NaBr). Samples were swollen with no ordering (micelle free), or they were collapsed with either several distinct peaks (cubic Pm3n) or one broad correlation peak (disordered micellar). The main factor determining the structure of the collapsed complexes was found to be the NaBr concentration, with the cubic structure existing up to approximately 150 mM NaBr and above which only the disordered micellar structure was found. Increasing the salt concentration decreases the polyion mediated attractive forces holding the micelles together causing swelling of the gel. At sufficiently high salt concentration the micelle-micelle distance in the gel becomes too large for the cubic structure to be retained, and it melts into a disordered micellar structure. As most samples were above the critical micelle concentration, the bulk of the surfactant was in the form of micelles in the solution and the surfactant concentration thereby had only a minor influence on the structure. However, in the region around 150 mM NaBr, increasing the surfactant concentration, at constant NaBr concentration, was found to change the structure from disordered micellar to ordered cubic and back to disordered again. PMID:17715959

  10. Regular and irregular deswelling of polyacrylate and hyaluronate gels induced by oppositely charged surfactants.

    Science.gov (United States)

    Nilsson, Peter; Hansson, Per

    2008-09-15

    The deswelling kinetics of macroscopic polyacrylate (PA) gels in solutions of dodecyltrimethylammonium bromide (C(12)TAB) and cetyltrimethylammonium bromide (C(16)TAB), with and without added sodium bromide, as well as hyaluronate (HA) gels in solutions of cetylpyridinium chloride (CPC) are investigated. Additional data are also provided by small-angle X-ray scattering and microgel experiments. The purpose is to study the deswelling behavior of (1) regularly deswelling gels, for which the deswelling is successfully described using a core/shell model earlier employed for microgels, and (2) irregularly deswelling gels, where the gel turns into a balloon-like structure with a dense outer layer surrounding a liquid-filled core. For regularly deswelling gels, the deswelling of PA/C(12)TAB is found to be controlled by diffusion through both stagnant layer and collapsed surface phase, while for PA/C(16)TAB it is found to be controlled mainly by the latter. The difference in deswelling rate between the two is found to correspond to the difference in surfactant diffusion coefficient in the surface phase. Factors found to promote irregular deswelling, described as balloon formation, are rapid surfactant binding, high bromide and surfactant concentration, longer surfactant chain length, and macroscopic gel size. Scattering data indicating a cubic structure for HA/CPC complexes are reported. PMID:18565536

  11. Efficiency of Sodium Polyacrylate to Improve Durability of Concrete under Adverse Curing Condition

    Directory of Open Access Journals (Sweden)

    Tanvir Manzur

    2015-01-01

    Full Text Available The conventional external curing process requires supply of large amount of water in addition to mixing water as well as strict quality control protocol. However, in a developing country like Bangladesh, many local contractors do not have awareness and required knowledge on importance of curing which often results in weaker concrete with durability issues. Moreover, at times it is difficult to maintain proper external curing process due to nonavailability of water and skilled laborer. Internal curing can be adopted under such scenario since this method is simple and less quality intensive. Usually, naturally occurring porous light weight aggregates (LWA are used as internal curing agent. However, naturally occurring LWA are not available in many countries like Bangladesh. Under these circumstances, Super Absorbent Polymer (SAP can be utilized as an alternative internal curing agent. In this study, sodium polyacrylate (SP as SAP has been used to produce internally cured concrete. Desorption isotherm of SP has been developed to investigate its effectiveness as internal curing agent. Test results showed that internally cured concrete with SP performed better in terms of both strength and durability as compared to control samples when subjected to adverse curing conditions where supply of additional water for external curing was absent.

  12. Recovery of nickel from aqueous solutions by complexation-ultrafiltration process with sodium polyacrylate and polyethylenimine.

    Science.gov (United States)

    Shao, Jiahui; Qin, Shu; Davidson, Joshua; Li, Wenxi; He, Yiliang; Zhou, H Susan

    2013-01-15

    The recovery of nickel from aqueous dilute solutions by complexation-ultrafiltration process with sodium polyacrylate (PAAS) and polyethylenimine (PEI) was studied. Experiments were performed as a function of aqueous pH, polymer/Ni(2+) ratio and background electrolyte concentration. At optimum experimental conditions, the nickel removal rate reaches 99.5% using PAAS and 93.0% using PEI as the complexation agent. The nickel removal rate was found to decrease as the adding salt NaCl concentration increases for both complexation agents. A series of experiments implied that the mechanism could be the compressing electric double layer other than the competitive complexation. Diafiltration technique was further performed to regenerate complexation agents and recover nickel. The nickel removal rates were found to be close to those obtained with the original PEI and PAAS. Finally, Langmuir-type binding isotherm equation was employed to evaluate the extent of nickel bound to PAAS and PEI. The overall results from the two-step process of complexation-UF and decomplexation-UF separation showed that it could be a promising method for nickel removal and recovery from aqueous solutions. PMID:23177250

  13. Superabsorbent biphasic system based on poly(lactic acid) and poly(acrylic acid)

    Science.gov (United States)

    Sartore, Luciana; Pandini, Stefano; Baldi, Francesco; Bignotti, Fabio

    2016-05-01

    In this research work, biocomposites based on crosslinked particles of poly(acrylic acid), commonly used as superabsorbent polymer (SAP), and poly-L-lactic acid (PLLA) were developed to elucidate the role of the filler (i.e., polymeric crosslinked particles) on the overall physico-mechanical behavior and to obtain superabsorbent thermoplastic products. Samples prepared by melt-blending of components in different ratios showed a biphasic system with a regular distribution of particles, with diameter ranging from 5 to 10 μm, within the PLLA polymeric matrix. The polymeric biphasic system, coded PLASA i.e. superabsorbent poly(lactic acid), showed excellent swelling properties, demonstrating that cross-linked particles retain their superabsorbent ability, as in their free counterparts, even if distributed in a thermoplastic polymeric matrix. The thermal characteristics of the biocomposites evidence enhanced thermal stability in comparison with neat PLLA and also mechanical properties are markedly modified by addition of crosslinked particles which induce regular stiffening effect. Furthermore, in aqueous environments the particles swell and are leached from PLLA matrix generating very high porosity. These new open-pore PLLA foams, produced in absence of organic solvents and chemical foaming agents, with good physico-mechanical properties appear very promising for several applications, for instance in tissue engineering for scaffold production.

  14. Mechanically stable thermally crosslinked poly(acrylic acid)/reduced graphene oxide aerogels.

    Science.gov (United States)

    Ha, Heonjoo; Shanmuganathan, Kadhiravan; Ellison, Christopher J

    2015-03-25

    Graphene oxide (GO) aerogels, high porosity (>99%) low density (∼3-10 mg cm(-3)) porous materials with GO pore walls, are particularly attractive due to their lightweight, high surface area, and potential use in environmental remediation, superhydrophobic and superoleophilic materials, energy storage, etc. However, pure GO aerogels are generally weak and delicate which complicates their handling and potentially limits their commercial implementation. The focus of this work was to synthesize highly elastic, mechanically stable aerogels that are robust and easy to handle without substantially sacrificing their high porosity or low density. To overcome this challenge, a small amount of readily available and thermally cross-linkable poly(acrylic acid) (PAA) was intermixed with GO to enhance the mechanical integrity of the aerogel without disrupting other desirable characteristic properties. This method is a simple straightforward procedure that does not include multistep or complicated chemical reactions, and it produces aerogels with mass densities of about 4-6 mg cm(-3) and >99.6% porosity that can reversibly support up to 10,000 times their weight with full recovery of their original volume. Finally, pressure sensing capabilities were demonstrated and their oil absorption capacities were measured to be around 120 g oil per g aerogel(-1) which highlights their potential use in practical applications. PMID:25714662

  15. Structure and properties of mixtures based on long chain polyacrylate and 1-alcohol composites

    International Nuclear Information System (INIS)

    A series of phase change materials (PCMs) based on long chain polyacrylate and 1-alcohol, i.e., poly (stearyl methacrylate) and 1-tetradecanol (PSMA/C14OH) were prepared through the solution-mixing method. Thermal energy storage capacity, thermal stability and morphology of PSMA/C14OH PCMs were characterized by Fourier transform infrared spectroscopy (FTIR), polarized optical microscopy (POM), field emission scanning electron microscopy (FE-SEM), differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). DSC results demonstrated that the heat of fusion of PSMA/C14OH PCMs increased from 85.9 to 172.3 J g−1 with the weight fraction of C14OH increasing from 20 to 80 wt%. And, the thermal stability also enhanced with PSMA weight. The spherulite (ca. 250 μm) in PSMA/C14OH composites containing 60 wt% C14OH proved the compatibility between PSMA and C14OH, indicating the cocrystallization behavior of alkyl side groups appeared. The cocrystallization behavior contributes the enhanced thermal stability of PSMA/C14OH PCMs, and it is suitable as the thermal energy storage materials in the future. - Highlights: • Heat storage capability of PSMA/C14OH PCMs increased with C14OH weight. • The spherulites exhibit the weight-dependence upon C14OH. • The thermal stability of PSMA/C14OH PCMs obviously improved

  16. Poly(acrylic acid) brushes pattern as a 3D functional biosensor surface for microchips

    Science.gov (United States)

    Wang, Yan-Mei; Cui, Yi; Cheng, Zhi-Qiang; Song, Lu-Sheng; Wang, Zhi-You; Han, Bao-Hang; Zhu, Jin-Song

    2013-02-01

    Poly(acrylic acid) (PAA) brushes, a novel three dimensional (3D) precursor layer of biosensor or protein microarrays, possess high protein loading level and low non-specific protein adsorption. In this article, we describe a simple and convenient way to fabricate 3D PAA brushes pattern by microcontact printing (μCP) and characterize it with FT-IR and optical microscopy. The carboxyl groups of PAA brushes can be applied to covalently immobilize protein for immunoassay. Thriving 3D space made by patterning PAA brushes thin film is available to enhance protein immobilization, which is confirmed by measuring model protein interaction between human immunoglobulin G (H-IgG) and goat anti-H-IgG (G-H-IgG) with fluorescence microscopy and surface plasmon resonance imaging (SPRi). As expected, the SPRi signals of H-IgG coating on 3D PAA brushes pattern and further measuring specific binding with G-H-IgG are all larger than that of 3D PAA brushes without pattern and 2D bare gold surface. We further revealed that this surface can be used for high-throughput screening and clinical diagnosis by label-free assaying of Hepatitis-B-Virus surface antibody (HBsAb) with Hepatitis-B-Virus surface antigen (HBsAg) concentration array chip. The linearity range for HBsAb assay is wider than that of conventional ELISA method.

  17. 低分子量聚丙烯酸钠研究进展%Research Progress of the Polyacrylic Acid Sodium with Low Molecular Weight

    Institute of Scientific and Technical Information of China (English)

    田媛媛; 韦莎

    2012-01-01

    The application of polyacrylic acid depended on the size of the molecular weight.The polyacrylic acid with low molecular weight,good water soluble and larger polarity,can combine to the polyvalent metal ion such as calcium and magnesium ions,and formation soluble anionic.Therefore,using polyacrylic acid with low molecular weight as water stabilizer had significant inhibition effect.The polymerization mechanism,synthesis methods and research status of the polyacrylic acid with low molecular weight were reviewed.In addition,the application prospect of polyacrylic acid was briefly introduced.%聚丙烯酸的用途与其分子量的大小有着密切的关系,而低分子量的聚丙烯酸具有良好的水溶性和较大的极性,能够结合水中的钙、镁等多价离子形成可溶的链状阴离子,因此,用其作水质稳定剂具有显著的防垢效果。本文综述了低分子量聚丙烯酸钠的聚合原理、合成方法及其研究现状,并对其在各领域应用前景作了简要介绍。

  18. Application of Series of Polyacrylic Acid Hydrogel Series%聚丙烯酸系列水凝胶的应用∗

    Institute of Scientific and Technical Information of China (English)

    刘展晴

    2015-01-01

    Polyacrylic acid series hydrogel prepared from a kind of water-soluble organic polymer solvent has got extensive application. The applications of polyacrylic acid series hydrogel in adsorption,water absorption and water retention agent,cooling gel, drug carrier and drug release, composite the polyacrylic acid of intelligent hydrogel, etc. ,were introduced in this paper.%聚丙烯酸是一种水溶性有机高分子,用它开发出的系列水凝胶已经得到了广泛的应用。本文介绍了聚丙烯酸系列水凝胶在吸附剂、吸水保水剂、制退热贴、药物释放及复合成智能水凝胶等方面的应用。

  19. Properties of polyacrylic acid-coated silver nanoparticle ink for inkjet printing conductive tracks on paper with high conductivity

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Qijin [Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang 315201 (China); Shen, Wenfeng, E-mail: wfshen@nimte.ac.cn [Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang 315201 (China); Xu, Qingsong [Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang 315201 (China); Tan, Ruiqin [Faculty of Information Science and Engineering, Ningbo University, Ningbo, Zhejiang 315211 (China); Song, Weijie, E-mail: weijiesong@nimte.ac.cn [Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang 315201 (China)

    2014-10-15

    Silver nanoparticles with a mean diameter of approximately 30 nm were synthesized by reduction of silver nitrate with triethanolamine in the presence of polyacrylic acid. Silver nanoparticle-based ink was prepared by dispersing silver nanoparticles into a mixture of water and ethylene glycol. The mechanism for the dispersion and aggregation of silver nanoparticles in ink is discussed. The strong electrostatic repulsions of the carboxylate anions of the adsorbed polyacrylic acid molecules disturbed the aggregation of metal particles in solutions with a high pH value (pH > 5). An inkjet printer was used to deposit this silver nanoparticle-based ink to form silver patterns on photo paper. The actual printing qualities of the silver tracks were then analyzed by variation of printing passes, sintering temperature and time. The results showed that sintering temperature and time are associated strongly with the conductivity of the inkjet-printed conductive patterns. The conductivity of printed patterns sintered at 150 °C increased to 2.1 × 10{sup 7} S m{sup −1}, which was approximately one third that of bulk silver. In addition, silver tracks on paper substrate also showed better electrical performance after folding. This study demonstrated that the resulting ink-jet printed patterns can be used as conductive tracks in flexible electronic devices. - Highlights: • An ink from silver nanoparticles coated with polyacrylic acid was prepared. • The ink was used for inkjet-printed tracks at varying printing parameters. • The conductivity of printed tracks sintered at 150 °C increased to 2.1 × 10{sup 7} S/m. • Mechanism for dispersion and aggregation of the nanoparticles in ink is discussed.

  20. Properties of polyacrylic acid-coated silver nanoparticle ink for inkjet printing conductive tracks on paper with high conductivity

    International Nuclear Information System (INIS)

    Silver nanoparticles with a mean diameter of approximately 30 nm were synthesized by reduction of silver nitrate with triethanolamine in the presence of polyacrylic acid. Silver nanoparticle-based ink was prepared by dispersing silver nanoparticles into a mixture of water and ethylene glycol. The mechanism for the dispersion and aggregation of silver nanoparticles in ink is discussed. The strong electrostatic repulsions of the carboxylate anions of the adsorbed polyacrylic acid molecules disturbed the aggregation of metal particles in solutions with a high pH value (pH > 5). An inkjet printer was used to deposit this silver nanoparticle-based ink to form silver patterns on photo paper. The actual printing qualities of the silver tracks were then analyzed by variation of printing passes, sintering temperature and time. The results showed that sintering temperature and time are associated strongly with the conductivity of the inkjet-printed conductive patterns. The conductivity of printed patterns sintered at 150 °C increased to 2.1 × 107 S m−1, which was approximately one third that of bulk silver. In addition, silver tracks on paper substrate also showed better electrical performance after folding. This study demonstrated that the resulting ink-jet printed patterns can be used as conductive tracks in flexible electronic devices. - Highlights: • An ink from silver nanoparticles coated with polyacrylic acid was prepared. • The ink was used for inkjet-printed tracks at varying printing parameters. • The conductivity of printed tracks sintered at 150 °C increased to 2.1 × 107 S/m. • Mechanism for dispersion and aggregation of the nanoparticles in ink is discussed

  1. Radiation Induced Polyvinylpyrrolidone/Polyacrylic Acid Nano-Gel Formation for Biomedical Applications

    International Nuclear Information System (INIS)

    Adopting polyvinylpyrrolidone as template macromolecules and acrylic acid (AA) as monomers, at a concentration ranged from .05 to 1.5%, pH sensitive nano-particle colloids were successfully prepared via template polymerization using gamma radiation in which polymerization of the monomer and self-assembly between the polymer and the template take place simultaneously. The self-assembly was driven by specific interactions between PVP and PAA produced in-situ, leading to PVP/PAAc nano-particles with insoluble inter-polymer complexes. Dynamic light scattering technique was used to indicate size shrinkage and surface charge increase of the PVP/PAAc nano-particles. Many factors affecting the PVP/PAAc nano-particle size such as irradiation dose rate, exposure dose, irradiation temperature and atmosphere, PVP MWt, and feed composition and concentration were investigated. It was found that the reactant feed composition and irradiation temperatures have a great influence on particle size of the prepared nanogel. The structure and morphology of the nano-particles were characterized by FT-IR, UV, viscometry and AFM methods. The structure stability of the nano-particles was studied at different pH solutions. The nano-particles exhibit excellent pH response. When pH changed from acid to base, the particles‘ volume expanded 100 times depending on the irradiation dose at which the nanogel was prepared. The prepared nanogel was loaded with flutamide anticancer drug in the presence of ethanol-water mixture solution and the amount of loaded flutamide was determined. The prepared nano scale polyvinylpyrrolidone/polyacrylic acid bio-polymeric system loaded with flutamide drug is being investigated as anticancer target drug. Also this system will be tested for the treatment of dry-eye-syndrome. (author)

  2. Comb-shaped single ion conductors based on polyacrylate ethers and lithium alkyl sulfonate

    International Nuclear Information System (INIS)

    Comb-shaped single ion conductors have been synthesized by (1) sulfonation of small molecule chloroethyleneglycols, which, after ion exchange to the Li+ salt were then converted to the acrylate by reaction with acryloyl chloride and copolymerized with polyethylene glycol monomethyl ether acrylate (Mn = 454, n = 8) (PAE8-co-E3SO3Li); (2) sulfonation of chloride end groups grafted on to prepolymers of polyacrylate ethers (PAE8-g-EnSO3Li, n = 2, 3). The highest conductivity at 25 deg. C of 2.0 x 10-7 S cm-1 was obtained for the PAE8-co-E3SO3Li with a salt concentration of EO/Li = 40. The conductivity of PAE8-g-E3SO3Li is lower than that of PAE8-co-E3SO3Li at similar salt concentrations, which is related to the incomplete sulfonation of the grafted polymer that leads to a lower concentration of Li+. The addition of 50 wt.% of plasticizer, PC/EMC (1/1, v/v), to PAE8-g-E2SO3Li increases the ambient conductivity by three orders of magnitude, which is due to the increased ion mobility in a micro-liquid environment and an increase concentration of free ions as a result of the higher dielectric constant of the solvent. A symmetrical Li/Li cell with an electrolyte membrane consisting of 75 wt.% PC/EMC (1/1, v/v) was cycled at a current density of 100 μA cm-2 at 85 deg. C. The cycling profile showed no concentration polarization after a break-in period during the first few cycles, which was apparently due to reaction of the solvent at the lithium metal surface that reacted with lithium metal to form a stable SEI layer

  3. An NMR study of sodium poly(acrylate) adsorption on rutile

    International Nuclear Information System (INIS)

    Adsorption of sodium poly(acrylate) (PA) on rutile particles in aqueous dispersion was studied. Two different molecular weights of PA (2,100 and 30,000) and two different grades of rutile were used. Various pHs, ionic strengths, and PA concentrations were investigated. The main technique employed was measurement of the transverse NMR relaxation of the solvent using the CPMG pulse sequence. Other techniques used to augment these results include electroacoustics, scanning electron microscopy, and measurement of the adsorbed amount of PA by a fluorescence spectroscopy technique using the dye acridine orange. Adsorption of small ions such as Na+, K+, Cl-, and NO3- to the particle surface was found to have a significant effect on the measured transverse relaxation rate, that was dependent on the pH and the concentration of the ions. There was usually an additional effect on the relaxation due to the adsorbed PA, but only qualitative rather than quantitative information about the adsorption could be deduced. At pH 4 especially, it could be seen that the results were consistent with the common assertion that polymers adsorb in a flat conformation at low concentration, and only become looped when all of the surface sites are full. At pH 10 it was found that the relaxation rate for the longer chain PA samples fluctuated over time, indicating metastable PA conformations. There were also unusual trends in the relaxation rate for these samples, which could be due to a previously proposed small ion complexation mechanism for PA adsorption at high pH in this system. It is possible that an extensive and comprehensive study using this technique, investigating all of the relevant parameters, especially the effect of small ion adsorption, may allow a quantitative description of the adsorbed conformation. (author)

  4. Electron-beam induced RAFT-graft polymerization of poly(acrylic acid) onto PVDF

    International Nuclear Information System (INIS)

    This paper explores for the first time the post-radiation-induced-graft polymerization on solid substrate using reversible addition-fragmentation transfer (RAFT) mechanism. Radiation-induced graft polymerization onto polymers is a potentially interesting technique to create easily new materials from highly resistant polymers, e.g. surface graft polymerization of acrylic acid (AA) onto poly(vinylidene difluoride) (PVDF) improves its surface properties without losing its excellent mechanical properties. As a consequence of the radical nature of the polymerization processes it is difficult to control molecular weight of grafted chains, and therefore design and standardize the properties of the final product. RAFT polymerization is a suitable method to obtain monodisperse polymers. The ability of the RAFT agents to control the polymer chain length could be an interesting approach to improve the grafted polymers obtained by post-radiation-induced-graft polymerization technique. In this way, graft polymerization of AA onto electron-beam irradiated α-PVDF was performed using trithiocarbonic acid bis(1-phenylethyl) ester as a RAFT agent to control the radical polymerization. We studied several grafting parameters such as solvent, monomer concentration and grafting time in order to achieve a poly(acrylic acid) (PAA) layer onto PVDF surface. Acetic acid was found to be the best solvent for many reasons, as to drive graft polymerization mainly to the polymer surface, complete solubility and stability of all reactants. Hydrolysis of PAA chains was also studied in order to remove the trithiocarbonate functionality from the grafted polymer. A mild chemical condition was achieved in order to have thiol groups that were detected onto the modified PVDF by specific enzymatic reaction

  5. Electron-beam induced RAFT-graft polymerization of poly(acrylic acid) onto PVDF

    Science.gov (United States)

    Grasselli, M.; Betz, N.

    2005-07-01

    This paper explores for the first time the post-radiation-induced-graft polymerization on solid substrate using reversible addition-fragmentation transfer (RAFT) mechanism. Radiation-induced graft polymerization onto polymers is a potentially interesting technique to create easily new materials from highly resistant polymers, e.g. surface graft polymerization of acrylic acid (AA) onto poly(vinylidene difluoride) (PVDF) improves its surface properties without losing its excellent mechanical properties. As a consequence of the radical nature of the polymerization processes it is difficult to control molecular weight of grafted chains, and therefore design and standardize the properties of the final product. RAFT polymerization is a suitable method to obtain monodisperse polymers. The ability of the RAFT agents to control the polymer chain length could be an interesting approach to improve the grafted polymers obtained by post-radiation-induced-graft polymerization technique. In this way, graft polymerization of AA onto electron-beam irradiated α-PVDF was performed using trithiocarbonic acid bis(1-phenylethyl) ester as a RAFT agent to control the radical polymerization. We studied several grafting parameters such as solvent, monomer concentration and grafting time in order to achieve a poly(acrylic acid) (PAA) layer onto PVDF surface. Acetic acid was found to be the best solvent for many reasons, as to drive graft polymerization mainly to the polymer surface, complete solubility and stability of all reactants. Hydrolysis of PAA chains was also studied in order to remove the trithiocarbonate functionality from the grafted polymer. A mild chemical condition was achieved in order to have thiol groups that were detected onto the modified PVDF by specific enzymatic reaction.

  6. Preparation of carboxymethyl chitosan grafted polyacrylic acid hydrogel and its evaluation in vitro and in vivo

    Directory of Open Access Journals (Sweden)

    Yuqin CUI

    2015-10-01

    Full Text Available A novel pH-sensitive carboxymethyl chitosan graft polyacrylic acid(CMC-g-PAA hydrogel is fabricated via a free radical heat-initiated graft copolymerization reaction with acrylic acid(AA and carboxymethyl chitosan(CMC as monomers. The polymerization is successful, which is confirmed via fourier transform infrared spectroscopy (FT-IR. The result of swelling experiment indicates that the final CMC-g-PAA hydrogel has significant pH-sensitivity. Insulin(INS, as a model drug, is loaded into the hydrogel and 216.5 mg/g incorporation of INS is obtained. In vitro release profiles suggest that INS release is (16.3±2.6% when pH is 1.2 after 2 h. INS release is (57.2±3.5% in PBS with pH of 7.4 after the next 2 h. The study indicates that the CMC-g-PAA hydrogel loaded with INS could targeted deliver INS in intestinal, and avoid that INS is destroyed by gastric acid and pepsin. The experiment result on animals indicates that the CMC-g-PAA hydrogel loaded with INS has hypoglycemic effects. With different concentrations of CMC-g-PAA hydrogel co-cultured with Caco-2 cells, the cell survival rates are close to 100%, which indicates that the hydrogel has no cytotoxicity. In sum, the novel CMC-g-PAA hydrogel has a prospective application in the specific-site delivery of proteins and peptides.

  7. The Fouling of Zirconium(IV Hydrous Oxide–Polyacrylate Dynamically Formed Membranes during the Nanofiltration of Lactic Acid Solutions

    Directory of Open Access Journals (Sweden)

    Ewa Polom

    2013-12-01

    Full Text Available The results of investigations of flux decline during nanofiltration (NF of lactic acid solutions using dynamically formed zirconium(IV hydrous oxide/polyacrylate membranes (Zr(IV/PAA under conditions resulting in low and high lactic acid rejection are reported. The experimental permeate flux versus time curves were analyzed in the frame of resistance in a series model with the aim of developing the characteristic of resistances. Analysis of experimental data and results of calculations showed that the reduction of fouling effects in the investigated system could be achieved due to appropriate hydrodynamic process conditions and regular rinsing with deionized water.

  8. Synthesis of polyacrylate/polyethylene glycol interpenetrating network hydrogel and its sorption of heavy-metal ions

    OpenAIRE

    Qunwei Tang, Xiaoming Sun, Qinghua Li, Jihuai Wu and Jianming Lin

    2009-01-01

    A simple two-step aqueous polymerization method was introduced to synthesize a polyacrylate/polyethylene glycol (PAC/PEG) interpenetrating network (IPN) hydrogel. On the basis of the effects of the ratio of PAC to PEG, neutralization degree, heavy-metal ion concentration, and temperature on the adsorption behavior of PAC/PEG IPN hydrogel toward Ni2 +, Cr3 + and Cd2 +, the preparation conditions were optimized. In our system, the greatest amount of Ni2 +, Cr3 + and Cd2 + adsorbed were 102.34, ...

  9. STUDY ON MAGNETIC FIELD-INDUCED ORIENTATION OF A CHIRAL SIDE-CHAIN LIQUID CRYSTAL POLYACRYLATE USING INFRARED DICHROISM

    Institute of Scientific and Technical Information of China (English)

    HE Liu; JIN Shunzi; ZHANG Shufan; QI Zongneng; WANG Fosong

    1996-01-01

    Magnetic field-induced orientation of a chiral side chain liquid crystalline polyacrylate (P-11) was studied by using IR dichroism. For the investigated P-11, it has been shown that the magnetic alignment takes place over the entire temperature range between its melting point and clearing point and the orientation level is strongly temperature-dependent, the development with time of the magnetic orientation follows an exponential-type relation,and the smectic phase state influences the thermal relaxation process in the absence of the magnetic field.

  10. Phase Diagrams of the Aqueous Two-Phase Systems of Poly(ethylene glycol)/Sodium Polyacrylate/Salts

    OpenAIRE

    Adalberto Pessoa Junior; Hans-Olof Johansson; Eloi Feitosa

    2011-01-01

    Aqueous two-phase systems consisting of polyethylene glycol (PEG), sodium polyacrylate (NaPAA), and a salt have been studied. The effects of the polymer size, salt type (NaCl, Na2SO4, sodium adipate and sodium azelate) and salt concentrations on the position of the binodal curve were investigated. The investigated PEG molecules had a molar mass of 2,000 to 8,000 g/mol, while that of NaPAA was 8,000 g/mol. Experimental phase diagrams, and tie lines and calculated phase diagrams, based on Flory...

  11. Effect of trans-cis photoisomerization on phase equilibria and phase transition of liquid-crystalline azobenzene chromophore and its blends with reactive mesogenic diacrylate.

    Science.gov (United States)

    Kim, Namil; Li, Quan; Kyu, Thein

    2011-03-01

    Photoisomerization-induced phase transition of neat liquid-crystalline azobenzene chromophore (LCAC) and its effect on phase diagrams of its mixtures with reactive mesogenic diacrylate monomer (RM257) have been investigated experimentally and theoretically. Upon irradiation with ultraviolet light, the nematic phase of LCAC transformed to isotropic, while the crystal phase showed corrugated textures on the surface (i.e., ripples). The phase-transition temperatures and corresponding morphologies of the blends have been investigated by means of differential scanning calorimetry and optical microscopy. A theoretical phase diagram of a binary nematic and crystalline system was constructed by self-consistently solving the combined free energies of Flory-Huggins, Maier-Saupe, and phase-field theory. The calculation revealed various coexistence regions such as nematic + liquid (N₁ + L₂), crystal + liquid (Cr₁ + L₂), crystal + nematic (Cr₁ + N₂), and crystal + crystal (Cr₁ + Cr₂) over a broad range of compositions including the single-phase nematic (N₁, N₂) of the corresponding constituents. The calculated liquidus lines were in good accord with the depressed mesophase-isotropic transition points. The present paper demonstrates the effect of trans-cis photoisomerization on the mesophase transitions of neat LCAC and the phase diagram of LCAC-RM257 as well as on the ripple formation (i.e., periodic undulation) on the azobenzene crystals. PMID:21517513

  12. 偶氮苯聚氨酯基抗皱功能高分子染料制备及性能%Synthesis and properties of azobenzene-polyurethane based anti-wrinkle polymeric dye

    Institute of Scientific and Technical Information of China (English)

    冒海燕; 张淼; 强思雨; 杨小祥; 王潮霞; 殷允杰

    2016-01-01

    为同步实现纺织品着色与功能整理并改善低分子染料的耐热迁移性,通过共价键合方式将N, N-二羟乙基偶氮苯发色体引入聚氨酯分子链,制备具有抗皱功能的偶氮苯聚氨酯基高分子染料.结果表明,偶氮苯发色体的反应率为87.81%,占聚氨酯链的3.53%,偶氮苯聚氨酯基高分子染料色光未发生变化,且涂层织物色泽鲜艳饱满,K/S值从1.50提高到4.61,急弹折皱回复角从110º增加到183º,缓弹折皱回复角从136º提高到227º,且热迁移率下降至5%,因此,偶氮苯聚氨酯基高分子染料不仅具有良好的抗皱性及耐热迁移性,而且为缩短纺织品生产工艺流程提供了一条新途径.%Azobenzene-polyurethane based polymeric dye with anti-wrinkle property was prepared by covalently bonding N,N-di(2-hydroxyethyl) azobenzene with polyurethane chain to synchronously realize coloring and functional finishing and enhance the thermal migration. Results showed that reaction rate of azobenzene and its content in polyurethane chain were 87. 81% and 3. 53%, respectively. The color remained unchanged after the azobenzene was introduced into polyurethane. The coated cotton fabric with the azobenzene-polyurethane polymeric dye presented more vivid and richer shade than that with azobenzene physically mixed polyurethane, and the K/S value increased from 1. 50 to 4. 61. The fast and delayed elastic recovery angles of the coated fabric were improved from 110 º to 183 º and 136 º to 227 º , respectively. The thermal migration rate was dramatically reduced to 5%. Consequently, the azobenzene-polyurethane polymeric dye exhibited outstanding anti-wrinkle property and thermal migration property, which provided a novel route for shortening the textile technological process.

  13. Radiation Synthesis of Poly(N-Vinyl Pyrrolidone) Nanogels and Nanoscale Grafting of Poly(Acrylic Acid) from Cellulose

    International Nuclear Information System (INIS)

    Ionizing radiation has long been known to be a very useful tool for the preparation of nanogels. Although preparation is straightforward, the control of the sizes of nanogels has been a challenging issue. This report shows the results of our work on using radiation for the synthesis of PVP nanogels in the range of 40-200nm by making use of the principles of solution thermodynamics of aqueous polymer solutions. Nanoscale grafting of responsive polymers however has been of scientific and industrial importance due to fine control of the molecular weight and molecular weight distribution of grafted polymers. The second part of this report deals with the grafting of poly(acrylic acid) onto the surface of cellulose, thus imparting pH response to the substrate. The use of radiation as a constant source of radical generation and Reversible-Addition-Fragmentation-Chain transfer agents for the control of free radical polymerization provided a full control over the molecular weight and distribution of poly(acrylic acid) grafts on cellulose. (author)

  14. Dye-sensitized solar cell with poly(acrylic acid-co-acrylonitrile)-based gel polymer electrolyte

    International Nuclear Information System (INIS)

    Highlights: ► A nontoxic, easily synthesized poly(acrylic acid-co-acrylonitrile) showed suitable transmittance for dye-sensitized solar cell. ► A cell with relatively large active area fabricated with this polymer material showed acceptable efficiency. ► The gel polymer matrix affected the charge recombination, I3− diffusion, double layer capacitance, and electron lifetime in the cell. - Abstract: A non-conducting, nontoxic poly(acrylic acid-co-acrylonitrile) (PAA) was prepared and used as a supporting matrix for the electrolyte of dye-sensitized solar cells (DSSCs). DSSCs of active area 0.80 cm × 1.10 cm fabricated with PAA, 0.5 M LiI, 0.05 M I2, 0.5 M 3-tert-butylpyridine, and 0.1 M 1-methyl-3-propylimidazolium iodide in 3-methoxypropionitrile solvent showed an average solar energy conversion efficiency of 1.61% under simulated sunlight illumination of 100 mW cm−2, AM 1.5. The effects of the gel polymer matrix on the electrochemical properties of DSSCs were studied using the electrochemical impedance spectroscopy. Relative to the non-gel reference cells, the results showed a decrease in charge recombination, ionic diffusion, and double layer capacitance and an increase in electron lifetime. These results could play an important role in determining the future direction for the development of high-performance gel polymer electrolytes.

  15. Membrane Made of Cellulose Acetate with Polyacrylic Acid Reinforced with Carbon Nanotubes and Its Applicability for Chromium Removal

    Directory of Open Access Journals (Sweden)

    J. A. Sánchez-Márquez

    2015-01-01

    Full Text Available Membranes made of carbon nanotubes and cellulose acetate with polyacrylic acid were designed in order to study their properties and their applicability for chromium removal. The membranes were prepared by phase inversion method using cellulose acetate and polyacrylic acid. Carbon nanotubes were added to the membrane during their process of synthesis in proportions of 1% by weight. The pores in the material are formed in layers, giving the effect of depth and forming a network. Both the carbon nanotubes and membranes were characterized by IR, Raman, and SEM spectroscopy. In addition, the concentration of acidic and basic sites and the surface charge in the materials were determined. The concentration of acid sites for oxidized nanotubes was 4.0 meq/g. The removal of Cr(VI was studied as a function of contact time and of initial concentration of Cr(VI. The removal of Cr(VI (~90% mainly occurs in a contact time from 32 to 64 h when the initial concentration of Cr(VI is 1 mg/L.

  16. Quartz crystal microbalance and infrared reflection absorption spectroscopy characterization of bisphenol A absorption in the poly(acrylate) thin films.

    Science.gov (United States)

    Li, Guifeng; Morita, Shigeaki; Ye, Shen; Tanaka, Masaru; Osawa, Masatoshi

    2004-02-01

    The absorption process of bisphenol A (BPA) in a number of poly(acrylate) thin films, such as poly(2-methoxyethyl acrylate) (PMEA), poly(ethyl acrylate) (PEA), poly(n-butyl methacrylate) (PBMA), and poly(methyl methacrylate) (PMMA), has been investigated by quartz crystal microbalance (QCM) and infrared reflection absorption spectroscopy (IRRAS) measurements. Both QCM and IRRAS measurements show that the BPA molecules absorb in PMEA, PEA, and PBMA thin films but not in PMMA thin film. The differences in the BPA absorption behavior are mainly attributed to the difference in the glass transition temperature (T(g)) between these polymers. This absorption behavior also depends on the BPA concentration and polymer film thickness. Furthermore, IRRAS characterization demonstrates that the hydrogen bonding is formed between the hydroxyl group in BPA and the carbonyl group in the poly(acrylate) thin films. BPA molecule absorbed in these polymer thin films can be removed by ethanol rinse treatment. By optimizing experimental conditions for the QCM electrode modified by PMEA thin film, detection limitation of approximately 1 ppb for BPA can be realized by the in situ QCM measurement. This method is expected to be a sensitive in situ detection way for trace BPA in the environmental study. PMID:14750877

  17. Cobalt magnetic nanoparticles embedded in carbon matrix: biofunctional validation

    International Nuclear Information System (INIS)

    Carbon nanostructures and nanocomposites display versatile allotropic morphologies, physico-chemical properties and have a wide range of applications in mechanics, electronics, biotechnology, structural material, chemical processing, and energy management. In this study we report the synthesis, characterization, and biotechnological application of cobalt magnetic nanoparticles, with diameter approximately 15–40 nm, embedded in carbon structure (Co/C-MN). A single-step chemical process was used in the synthesis of the Co/C-MN. The Co/C-MN has presented superparamagnetic behavior at room temperature an essential property for immunoseparation assays carried out here. To stimulate interactions between proteins and Co/C-MN, this nanocomposite was functionalized with acrylic acid (AA). We have showed the bonding of different proteins onto Co/C-AA surface using immunofluorescence assay. A Co/C-AA coated with monoclonal antibody anti-pathogenic Leptospira spp. was able to capture leptospires, suggesting that it could be useful in immunoseparation assays.

  18. Silver-nanoparticle-embedded antimicrobial paints based on vegetable oil

    Science.gov (United States)

    Kumar, Ashavani; Vemula, Praveen Kumar; Ajayan, Pulickel M.; John, George

    2008-03-01

    Developing bactericidal coatings using simple green chemical methods could be a promising route to potential environmentally friendly applications. Here, we describe an environmentally friendly chemistry approach to synthesize metal-nanoparticle (MNP)-embedded paint, in a single step, from common household paint. The naturally occurring oxidative drying process in oils, involving free-radical exchange, was used as the fundamental mechanism for reducing metal salts and dispersing MNPs in the oil media, without the use of any external reducing or stabilizing agents. These well-dispersed MNP-in-oil dispersions can be used directly, akin to commercially available paints, on nearly all kinds of surface such as wood, glass, steel and different polymers. The surfaces coated with silver-nanoparticle paint showed excellent antimicrobial properties by killing both Gram-positive human pathogens (Staphylococcus aureus) and Gram-negative bacteria (Escherichia coli). The process we have developed here is quite general and can be applied in the synthesis of a variety of MNP-in-oil systems.

  19. Optoelectronic device with nanoparticle embedded hole injection/transport layer

    Science.gov (United States)

    Wang, Qingwu; Li, Wenguang; Jiang, Hua

    2012-01-03

    An optoelectronic device is disclosed that can function as an emitter of optical radiation, such as a light-emitting diode (LED), or as a photovoltaic (PV) device that can be used to convert optical radiation into electrical current, such as a photovoltaic solar cell. The optoelectronic device comprises an anode, a hole injection/transport layer, an active layer, and a cathode, where the hole injection/transport layer includes transparent conductive nanoparticles in a hole transport material.

  20. Laser-generated plasma by carbon nanoparticles embedded into polyethylene

    Czech Academy of Sciences Publication Activity Database

    Torrisi, L.; Ceccio, G.; Cutroneo, Mariapompea

    2016-01-01

    Roč. 375, MAY (2016), s. 93-99. ISSN 0168-583X R&D Projects: GA ČR(CZ) GBP108/12/G108; GA MŠk(CZ) LM2011019 Institutional support: RVO:61389005 Keywords : carbon nanoparticles * laser -generated plasma * Time-of-flight measurements * advanced targets Subject RIV: BG - Nuclear, Atomic and Molecular Physics , Colliders Impact factor: 1.124, year: 2014

  1. Synthesis and characterization of magnetic nanoparticles embedded in polyacrylonitrile nanofibers

    Science.gov (United States)

    Munteanu, Daniel; Ion, Rodica-Mariana; Cocina, George-Costel

    2010-11-01

    Nanomedicine is defined as the monitoring, repair, construction, and control of human biological systems at the molecular level using engineered nanodevices and nanostructures. Polyacrylonitrile (PAN) solution containing the iron oxide precursor iron (III) was electrospun and thermally treated to produce electrically conducting, magnetic carbon nanofiber mats with hierarchical pore structures. This paper discusses the synthesis of magnetite (Fe3O4) nanoparticles with mean crystallite size of 10 nm with polyacrylonitrile (PAN) as the protecting agent, creating nanofiber. The morphology and material properties of the resulting multifunctional nanofiber including the surface area were examined using various characterization techniques. Optical microscopy images show that uniform fibers were produced with a fiber diameter of ~600 nm, and this uniform fiber morphology is maintained after graphitization with a fiber diameter of ~330 nm. X-ray diffraction (XRD) studies reveal the size of Fe3O4 crystals. A combination of XRD and electron microscopy experiments reveals the formation of pores with graphitic nanoparticles in the walls as well as the formation of magnetite nanoparticles distributed throughout the fibers.

  2. Germanium nanowires and germanium nanoparticles embedded into hydrogenated silicon matrix

    Czech Academy of Sciences Publication Activity Database

    Stuchlíková, The-Ha; Dřínek, Vladislav; Remeš, Zdeněk; Stuchlík, Jiří

    Cairn: IPCS International Plasma Chemistry Society, 2013. (IPSC. 21). ISBN N. [International Symposium on Plasma Chemistry (ISPC 21)/21./. Cairns Convention Centre (AU), 04.08.2013-09.08.2013] R&D Projects: GA MŠk LH12236; GA ČR GA13-25747S Grant ostatní: AVČR(CZ) M100101216; AVČR(CZ) M100101217 Institutional support: RVO:68378271 ; RVO:67985858 Keywords : nanowires * quantum dots * matrix * CVD * PECVD * LA Subject RIV: BM - Solid Matter Physics ; Magnetism

  3. Gold nanoparticles embedded silicon channel biosensor for improved sensitivity

    Science.gov (United States)

    Chang, H. Y.; Arshad, M. K. Md.; M. Nuzaihan M., N.; Fathil, M. F. M.; Hashim, U.

    2016-07-01

    This project discusses the fabrication steps of a biosensor device on silicon-on-insulator (SOI) wafer. Conventional photolithography technique is used to fabricate the device. The gold nanoparticles (GNPs) are then used to enhance the sensitivity of the device. By incorporating the GNPs, it is expected to get higher current compared with the device without GNPs due to better conductivity of gold and higher volume-to-ratio. Hence, with the addition of GNPs, it may boost up the signal and enhance the sensitivity of the device.

  4. Optical Fiber Sensors Based on Nanoparticle-Embedded Coatings

    Directory of Open Access Journals (Sweden)

    Aitor Urrutia

    2015-01-01

    Full Text Available The use of nanoparticles (NPs in scientific applications has attracted the attention of many researchers in the last few years. The use of NPs can help researchers to tune the physical characteristics of the sensing coating (thickness, roughness, specific area, refractive index, etc. leading to enhanced sensors with response time or sensitivity better than traditional sensing coatings. Additionally, NPs also offer other special properties that depend on their nanometric size, and this is also a source of new sensing applications. This review focuses on the current status of research in the use of NPs within coatings in optical fiber sensing. Most used sensing principles in fiber optics are briefly described and classified into several groups: absorbance-based sensors, interferometric sensors, fluorescence-based sensors, fiber grating sensors, and resonance-based sensors, among others. For each sensor group, specific examples of the utilization of NP-embedded coatings in their sensing structure are reported.

  5. Nanoparticles embedded in hydrogenated amorphous silicon thin layers

    Czech Academy of Sciences Publication Activity Database

    Remeš, Zdeněk; Stuchlík, Jiří; Stuchlíková, The-Ha; Purkrt, Adam; Fajgar, Radek; Dřínek, Vladislav; Zhuravlev, K.; Galkin, N.G.

    Aachen : ICANS26, 2015 - (Carius, R.). s. 196-197 [International Conference on Amorphous and Nanocrystalline Semiconductors /26./ (ICANS26). 13.09.2015-18.09.2015, Aachen] R&D Projects: GA ČR(CZ) GA14-05053S; GA MŠk(CZ) LD14011; GA MŠk LH12236 Institutional support: RVO:68378271 ; RVO:67985858 Keywords : a-Si:H * LED * RLA * RDE Subject RIV: BM - Solid Matter Physics ; Magnetism

  6. Laser-generated plasma by carbon nanoparticles embedded into polyethylene

    Science.gov (United States)

    Torrisi, L.; Ceccio, G.; Cutroneo, M.

    2016-05-01

    Carbon nanoparticles have been embedded into polyethylene at different concentrations by using chemical-physical processes. The synthesized material was characterized in terms of physical modifications concerning the mechanical, compositional and optical properties. Obtained flat targets have been irradiated by Nd:YAG laser at intensities of the order of 1010 W/cm2 in order to generate non-equilibrium plasma in vacuum. The laser-matter interaction produces charge separation effects with consequent acceleration of protons and carbon ions. Plasma was characterized using time-of-flight measurements of the accelerated ions. Applications of the produced targets in order to generate carbon ion beams from laser-generated plasma are presented and discussed.

  7. Cobalt magnetic nanoparticles embedded in carbon matrix: biofunctional validation

    Energy Technology Data Exchange (ETDEWEB)

    Krolow, Matheus Z., E-mail: matheuskrolow@ifsul.edu.br [Universidade Federal de Pelotas, Engenharia de Materiais, Centro de Desenvolvimento Tecnologico (Brazil); Monte, Leonardo G.; Remiao, Mariana H.; Hartleben, Claudia P.; Moreira, Angela N.; Dellagostin, Odir A. [Universidade Federal de Pelotas, Nucleo de Biotecnologia, Centro de Desenvolvimento Tecnologico (Brazil); Piva, Evandro [Universidade Federal de Pelotas, Faculdade de Odontologia (Brazil); Conceicao, Fabricio R. [Universidade Federal de Pelotas, Nucleo de Biotecnologia, Centro de Desenvolvimento Tecnologico (Brazil); Carreno, Neftali L. V. [Universidade Federal de Pelotas, Engenharia de Materiais, Centro de Desenvolvimento Tecnologico (Brazil)

    2012-09-15

    Carbon nanostructures and nanocomposites display versatile allotropic morphologies, physico-chemical properties and have a wide range of applications in mechanics, electronics, biotechnology, structural material, chemical processing, and energy management. In this study we report the synthesis, characterization, and biotechnological application of cobalt magnetic nanoparticles, with diameter approximately 15-40 nm, embedded in carbon structure (Co/C-MN). A single-step chemical process was used in the synthesis of the Co/C-MN. The Co/C-MN has presented superparamagnetic behavior at room temperature an essential property for immunoseparation assays carried out here. To stimulate interactions between proteins and Co/C-MN, this nanocomposite was functionalized with acrylic acid (AA). We have showed the bonding of different proteins onto Co/C-AA surface using immunofluorescence assay. A Co/C-AA coated with monoclonal antibody anti-pathogenic Leptospira spp. was able to capture leptospires, suggesting that it could be useful in immunoseparation assays.

  8. Fabrication and characterization of stable superhydrophobic fluorinated-polyacrylate/silica hybrid coating

    Energy Technology Data Exchange (ETDEWEB)

    Li, Kunquan; Zeng, Xingrong, E-mail: psxrzeng@gmail.com; Li, Hongqiang; Lai, Xuejun

    2014-04-01

    Graphical abstract: - Highlights: • The superhydrophobic PFA/SiO{sub 2} coating was successfully fabricated by spraying. • The synthesized PFA latex showed core–shell structure and good dispersion. • The PFA/SiO{sub 2} coating showed good resistance to acid and base, weather and heat. • The superhydrophobic coating could be fabricated on various substrates. - Abstract: The core–shell fluorinated-polyacrylate (PFA) emulsion was synthesized through emulsion polymerization method and the superhydrophobic PFA/SiO{sub 2} hybrid coating was successfully fabricated on the slide glass by spraying the mixture of PFA emulsion and hydrophobic SiO{sub 2} particles using ethanol as cosolvent. The PFA emulsion was characterized by Fourier transform infrared spectroscopy (FTIR), dynamic light scattering (DLS), water contact angle (WCA), transmission electron microscopy (TEM), and the effects of SiO{sub 2} content on the wetting behavior and surface morphology of PFA/SiO{sub 2} hybrid coating were investigated. To evaluate the stability of the hybrid coating, the acid and base resistance, weatherability and thermal stability were also studied. Results showed that the obtained PFA latex exhibited a core–shell structure with a particle size of 134.1 nm and a narrow polydispersity of 0.03. With the increase of dodecafluoroheptyl methacrylate (DFMA) content in the latex shell from 0 wt% to 31.8 wt%, the WCA of the PFA film enlarged from 85° to 104°, indicating that the introduction of fluorinated monomer was effective in reducing the surface energy. By adding different amount of SiO{sub 2} particles, the surface morphology and wetting behavior of the PFA/SiO{sub 2} hybrid coatings could be controlled. When the mass ratio of SiO{sub 2} to PFA emulsion was 0.2, the surface roughness (Rq) increased to 173.6 nm and the wetting behavior of the surface became superhydrophobic with a WCA of 153°, resulted from the corporation of low surface energy and the binary nano

  9. Fabrication and characterization of stable superhydrophobic fluorinated-polyacrylate/silica hybrid coating

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • The superhydrophobic PFA/SiO2 coating was successfully fabricated by spraying. • The synthesized PFA latex showed core–shell structure and good dispersion. • The PFA/SiO2 coating showed good resistance to acid and base, weather and heat. • The superhydrophobic coating could be fabricated on various substrates. - Abstract: The core–shell fluorinated-polyacrylate (PFA) emulsion was synthesized through emulsion polymerization method and the superhydrophobic PFA/SiO2 hybrid coating was successfully fabricated on the slide glass by spraying the mixture of PFA emulsion and hydrophobic SiO2 particles using ethanol as cosolvent. The PFA emulsion was characterized by Fourier transform infrared spectroscopy (FTIR), dynamic light scattering (DLS), water contact angle (WCA), transmission electron microscopy (TEM), and the effects of SiO2 content on the wetting behavior and surface morphology of PFA/SiO2 hybrid coating were investigated. To evaluate the stability of the hybrid coating, the acid and base resistance, weatherability and thermal stability were also studied. Results showed that the obtained PFA latex exhibited a core–shell structure with a particle size of 134.1 nm and a narrow polydispersity of 0.03. With the increase of dodecafluoroheptyl methacrylate (DFMA) content in the latex shell from 0 wt% to 31.8 wt%, the WCA of the PFA film enlarged from 85° to 104°, indicating that the introduction of fluorinated monomer was effective in reducing the surface energy. By adding different amount of SiO2 particles, the surface morphology and wetting behavior of the PFA/SiO2 hybrid coatings could be controlled. When the mass ratio of SiO2 to PFA emulsion was 0.2, the surface roughness (Rq) increased to 173.6 nm and the wetting behavior of the surface became superhydrophobic with a WCA of 153°, resulted from the corporation of low surface energy and the binary nano/microstructure on the surface. The as-prepared PFA/SiO2

  10. Probing the extent of the Sr2+ ion condensation to anionic polyacrylate coils: A quantitative anomalous small-angle x-ray scattering study

    Science.gov (United States)

    Goerigk, G.; Huber, K.; Schweins, R.

    2007-10-01

    The shrinking process of anionic sodium polyacrylate (NaPA) chains in aqueous solution induced by Sr2+ counterions was analyzed by anomalous small-angle x-ray scattering. Scattering experiments were performed close to the precipitation threshold of strontium polyacrylate. The pure-resonant scattering contribution, which is related to the structural distribution of the Sr2+ counterions, was used to analyze the extent of Sr2+ condensation onto the polyacrylate coils. A series of four samples with different ratios [Sr2+]/[NaPA] (between 0.451 and 0.464) has been investigated. From the quantitative analysis of the resonant invariant, the amount of Sr cations localized in the collapsed phase was calculated with concentrations v¯ between 0.94×1017 and 2.01×1017cm-3 corresponding to an amount of Sr cations in the collapsed phase between 9% and 23% of the total Sr2+ cations in solution. If compared to the concentration of polyacrylate expressed in moles of monomers [NaPA], a degree of site binding of r =[Sr2+]/[NaPA] between 0.05 and 0.11 was estimated. These values clearly differ from r =0.25, which was established from former light scattering experiments, indicating that the counterion condensation starts before the phase border is reached and increases rather sharply at the border.

  11. Poly(glycidyl methacrylate) microspheres: preparation by poly(acrylic acid)-stabilized dispersion polymerization and effect of some reaction parameters

    Czech Academy of Sciences Publication Activity Database

    Koubková, Jana; Horák, Daniel

    2013-01-01

    Roč. 2, č. 3 (2013), s. 218-225. ISSN 2164-9634 R&D Projects: GA ČR GCP207/12/J013 Institutional support: RVO:61389013 Keywords : glycidyl methacrylate * dispersion polymerization * poly(acrylic acid) Subject RIV: CD - Macromolecular Chemistry

  12. 聚丙烯酸钠吸附含铜废水的研究%Study on copper(Ⅱ) adsorption by sodium polyacrylate in wastewater

    Institute of Scientific and Technical Information of China (English)

    杨帆; 高俊发

    2012-01-01

    用聚丙烯酸钠吸附含铜废水,考察了吸附剂用量、时间、温度、pH值对聚丙烯酸钠吸附铜性能的影响.结果表明,对含200 mg/L的高铜废水,吸附条件为温度50℃,聚丙烯酸钠量30 g/L,时间60 min,pH为6时,聚丙烯酸钠对其的吸附率为97.14%,最大吸附容量为8.35 mg/g.聚丙烯酸钠对Cu2的吸附具有Langmuir吸附特征,分子中的羧基与Cu2+发生了配位作用,吸附机理以单分子层化学吸附为主,吸附量受温度影响不大.%The adsorption properties of sodium polyacrylate ( PAAS ) to the copper (Ⅱ) cation in wastewater,the adsorption effect of sodium polyacrylate were studied by adsorbent dosage,time,temperature and pH. The results showed that the adsorbed ratio of the sodium polyacrylate was 97. 14% ,the adsorption capacity was 8.35 mg/g for the wastewater with the high content of copper (Ⅱ) cation 200 mg/L, the reaction temperature was 50℃ , the adsorbent dosage of the sodium polyacrylate were 30 g/L,the time was 60 min for adsorption,and the pH was 6 for the wastewater sample. The adsorption has Langmuir characteristics for the sodium polyacrylate adsorption of copper( Ⅱ) cation. The adsorption mechanism was mainly monomolecular layer chemical adsorption, the temperature has little effect on adsorption capacity.

  13. Luminescence and Magnetic Properties of Two Three-Dimensional Terbium and Dysprosium MOFs Based on Azobenzene-4,4′-Dicarboxylic Linker

    Directory of Open Access Journals (Sweden)

    Belén Fernández

    2016-02-01

    Full Text Available We report the in situ formation of two novel metal-organic frameworks based on terbium and dysprosium ions using azobenzene-4,4′-dicarboxylic acid (H2abd as ligand, synthesized by soft hydrothermal routes. Both materials show isostructural three-dimensional networks with channels along a axis and display intense photoluminescence properties in the solid state at room temperature. Textural properties of the metal-organic frameworks (MOFs have been fully characterized although no appreciable porosity was obtained. Magnetic properties of these materials were studied, highlighting the dysprosium material displays slightly frequency-dependent out of phase signals when measured under zero external field and under an applied field of 1000 Oe.

  14. Spectral Characteristics of Bent-Core Azobenzen Monomers%含偶氮基团的弯曲型分子的光谱特性研究

    Institute of Scientific and Technical Information of China (English)

    董寅; 沈冬; 郑致刚

    2012-01-01

    The azo (-N =N-) linkage has the particular thermochemistry and actinoche-mistry behavior, the azobenzene group can undergo reversible cis-trans isomerization under light irradiation and its nonlinear optical properties possess the potential applications in the aspects of molecular design, photofixation, photochromics, thermochromism, etc. The UV-Vis absorbance of sixteen bent-core or linear monomers containing azobenzene as side arms and substituted para/m-aminobenzoic acid as central units was studied. The angle of the bent-core molecules was simulated. The trans-form of azo compounds showed a strong band in the UV region (330~370 nm) and a weak band at 440~450 nm. It was found that it has a close relationship between the angle of the molecules and the UV-Vis absorption.%偶氮连接基团(-N=N-)有着特殊的热化学和光化学行为,在适当波长光的照射下,能发生可逆的顺反异构反应,从而发生吸收波长的变化.在分子设计、光定位、光致变色和热致变色等方面,偶氮连接基团的非线性光化学性质都有着潜在的应用价值.文章以含有偶氮基作为侧翼的弯曲型分子作为研究对象,比较了弯曲型和直线型分子的吸收光谱;并用计算机模拟计算了弯曲型分子的角度,发现分子弯曲角和紫外可见吸收光谱存在着密切的关系.

  15. A study on the swelling behavior of poly(acrylic acid) hydrogels obtained by electron beam crosslinking

    Energy Technology Data Exchange (ETDEWEB)

    Sheikh, N., E-mail: nasheikh@aeoi.org.i [Radiation Applications Research School, Nuclear Science and Technology Research Institute, P.O. Box 11365-3486, Tehran (Iran, Islamic Republic of); Jalili, L. [Polymer group, Technology and Engineering Department, Yazd University, Yazd (Iran, Islamic Republic of); Anvari, F. [Radiation Applications Research School, Nuclear Science and Technology Research Institute, Yazd (Iran, Islamic Republic of)

    2010-06-15

    Poly(acrylic acid) (PAA) hydrogels were prepared by using electron beam (EB) crosslinking of PAA homopolymer from its aqueous solutions. The swelling behavior of the hydrogels was studied as a function of the concentration of PAA solution, radiation dose, pH of the swelling medium and swelling time. Also the environmental pH effect on the water diffusion mode into hydrogels was investigated. These hydrogels clearly showed pH-sensitive swelling behavior with Fickian type of diffusion in the stomach-like pH medium (pH 1.3) and non-Fickian type in the intestine-like pH medium (pH 6.8).

  16. Surface grafted chitosan gels. Part I. Molecular insight into the formation of chitosan and poly(acrylic acid) multilayers

    DEFF Research Database (Denmark)

    Liu, Chao; Thormann, Esben; Claesson, Per M.;

    2014-01-01

    Composite polyelectrolyte multilayers of chitosan and low molecular weight poly(acrylic acid) (PAA) have been assembled by sequential adsorption as a first step toward building a surface anchored chitosan gel. Silane chemistry was used to graft the first chitosan layer to prevent film detachment...... and decomposition. The assembly process is characterized by nonlinear growth behavior, with different adsorption kinetics for chitosan and PAA. In situ analysis of the multilayer by means of surface sensitive total internal reflection Raman (TIRR) spectroscopy, combined with target factor analysis of...... steps. The higher molecular weight chitosan shows a similar behavior, although to a much lower extent. Our data demonstrate that the charged monomeric units of chitosan are mainly compensated by carboxylate ions from PAA. Furthermore, the morphology and mechanical properties of the multilayers were...

  17. Decolourization performance in C. I. Vat Yellow 1 aqueous suspension using hydrophobically modified poly(acrylic acid).

    Science.gov (United States)

    Chen, J; Chen, M C

    2011-01-01

    A series of hydrophobically modified poly(acrylic acid) (PAA), poly(2-phenoxyethyl acrylate-co-acrylic acid) (poly(PHEA-co-AA)), have been synthesized and characterized by Ubbelohde type viscometry, Nuclear Magnetic Resonance (1H NMR) spectrometry and Differential Scanning Calorimetry (DSC). The shear thinning Non-Newtonian fluid behavior of their aqueous solution and the dependence on pH and hydrophobic group contents were found through apparent viscosity and rheological property investigating. Decolourization performance in C. I. Vat Yellow 1 aqueous suspension was evaluated through visible absorbance data. Decolourization performance of hydrophobically associated polymer indicates two times better than that of PAA. The quantitative relationship was mainly studied. PMID:21866762

  18. Synthesis of polyacrylate/polyethylene glycol interpenetrating network hydrogel and its sorption of heavy-metal ions

    Directory of Open Access Journals (Sweden)

    Qunwei Tang, Xiaoming Sun, Qinghua Li, Jihuai Wu and Jianming Lin

    2009-01-01

    Full Text Available A simple two-step aqueous polymerization method was introduced to synthesize a polyacrylate/polyethylene glycol (PAC/PEG interpenetrating network (IPN hydrogel. On the basis of the effects of the ratio of PAC to PEG, neutralization degree, heavy-metal ion concentration, and temperature on the adsorption behavior of PAC/PEG IPN hydrogel toward Ni2 +, Cr3 + and Cd2 +, the preparation conditions were optimized. In our system, the greatest amount of Ni2 +, Cr3 + and Cd2 + adsorbed were 102.34, 49.38 and 33.41 mg g- 1, respectively. The adsorption abilities of a dried PAC/PEG composite and a swollen PAC/PEG IPN hydrogel were compared. It was found that the efficiency of removing metal ions using the swollen hydrogel was greater than that using the dried composite. The adsorption mechanism and model are also discussed.

  19. Synthesis of polyacrylate/polyethylene glycol interpenetrating network hydrogel and its sorption of heavy-metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Tang Qunwei; Sun Xiaoming; Li Qinghua; Wu Jihuai; Lin Jianming [Key Laboratory for Functional Materials of Fujian Higher Education, Institute of Material Physical Chemistry, Huaqiao University, Quanzhou 362021 (China)], E-mail: jhwu@hqu.edu.cn

    2009-01-15

    A simple two-step aqueous polymerization method was introduced to synthesize a polyacrylate/polyethylene glycol (PAC/PEG) interpenetrating network (IPN) hydrogel. On the basis of the effects of the ratio of PAC to PEG, neutralization degree, heavy-metal ion concentration, and temperature on the adsorption behavior of PAC/PEG IPN hydrogel toward Ni{sup 2+}, Cr{sup 3+} and Cd{sup 2+}, the preparation conditions were optimized. In our system, the greatest amount of Ni{sup 2 +}, Cr{sup 3 +} and Cd{sup 2 +} adsorbed were 102.34, 49.38 and 33.41 mg g{sup - 1}, respectively. The adsorption abilities of a dried PAC/PEG composite and a swollen PAC/PEG IPN hydrogel were compared. It was found that the efficiency of removing metal ions using the swollen hydrogel was greater than that using the dried composite. The adsorption mechanism and model are also discussed.

  20. The influence of pH, polyethylene glycol and polyacrylic acid on the stability of stem bromelain

    Directory of Open Access Journals (Sweden)

    Letícia Celia de Lencastre Novaes

    2014-04-01

    Full Text Available Enzyme stability is critical in biotechnology, pharmaceutical and cosmetic industries. Investigations on this subject have drawn attention because of its practical application. Bromelain is a thiol-endopeptidase, obtained from pineapple (Ananas comosus, known for its clinical and therapeutic applications, particularly to selective burn debridement and improvement of antibiotic action and anti-inflammatory activities. To date, the use of bromelain in pharmacological or industrial applications is limited, due to commercial availability, costs, and sensitivity to pH and temperature. Therefore, a better understanding of enzyme stability would be of great interest. The aim of this study was to evaluate bromelain activity and stability in several pH (2.0 to 8.0 and in polyethylene glycol and polyacrylic acid solutions. We observed that bromelain was able to maintain its stability at pH 5.0 for the temperatures studied. PEG solutions increased bromelain stability, but PAA solutions had the opposite effect.

  1. Phase Diagrams of the Aqueous Two-Phase Systems of Poly(ethylene glycol/Sodium Polyacrylate/Salts

    Directory of Open Access Journals (Sweden)

    Adalberto Pessoa Junior

    2011-03-01

    Full Text Available Aqueous two-phase systems consisting of polyethylene glycol (PEG, sodium polyacrylate (NaPAA, and a salt have been studied. The effects of the polymer size, salt type (NaCl, Na2SO4, sodium adipate and sodium azelate and salt concentrations on the position of the binodal curve were investigated. The investigated PEG molecules had a molar mass of 2,000 to 8,000 g/mol, while that of NaPAA was 8,000 g/mol. Experimental phase diagrams, and tie lines and calculated phase diagrams, based on Flory-Huggins theory of polymer solutions are presented. Due to strong enthalpic and entropic balancing forces, the hydrophobicity of the added salt has a strong influence on the position of the binodal, which could be reproduced by model calculations.

  2. Synthesis of hollow silver spheres using poly-(styrene-methyl acrylic acid) as templates in the presence of sodium polyacrylate

    Science.gov (United States)

    Wang, Aili; Yin, Hengbo; Ge, Chen; Ren, Min; Liu, Yumin; Jiang, Tingshun

    2010-02-01

    Hollow silver spheres were successfully prepared by reducing AgNO 3 with ascorbic acid and using negatively charged poly-(styrene-methyl acrylic acid) (PSA) spheres as templates in the presence of sodium polyacrylate as a stabilizer. Firstly, silver cations adsorbed on the surface of PSA spheres via electrostatic attraction between the carboxyl groups and silver cations were reduced in situ by ascorbic acid. The silver nanoparticles deposited on the surface of PSA spheres served as seeds for the further growth of silver shells. After that, extra amount of AgNO 3 and ascorbic acid solutions were added to form PSA/Ag composites with thick silver shells. In order to obtain compact silver shells, the as-prepared PSA/Ag composites were heated at 150 °C for 3 h. Then hollow silver spheres were prepared by dissolving PSA templates with tetrahydrofuran.

  3. Determination of superabsorbent polyacrylate dust in workplace atmospheres after derivatization with ethanol and using HPLC with pulsed electrochemical detection.

    Science.gov (United States)

    Wink, O; Schack, F

    2000-10-01

    Superabsorbent polyacrylates (SAPs) have been used in the hygiene industry for many years. A derivatization and analytical method was developed for routine analysis of trace levels of SAP dust in workplace atmospheres. In comparison with existing methods, which are based on the sodium content or the ion exchange properties of the polymer, this method is more specific. It has the advantage of not being influenced by any sodium containing contaminants. Air samples are collected on Teflon filters using air monitoring sampling cassettes. The filters are subsequently placed in quartz vials and a reaction mixture containing hydrochloric acid in ethanol is added. The hydrochloric acid-ethanol solution, when heated, converts the carboxylic acid groups on the backbone of the insoluble polyacrylate into ethyl esters. After reaction, the excess of ethanol and hydrochloric acid is completely removed under vacuum. The sample is then treated with aqueous sodium hydroxide at 80 degrees C to release the bound ethanol. The solution is analyzed by HPLC on an anion exclusion stationary phase using dilute perchloric acid as mobile phase. Ethanol is identified and quantified with a pulsed electrochemical detector. Several environmental samples in addition to laboratory spiked samples were successfully analyzed with this technique. Recoveries averaged > 85% for spiked blank filters at levels from 5 to 50 micrograms per filter with relative standard deviations up to 7%. The instrument's limit of detection (LOD) for ethanol was 0.1 mg l-1. The LOD for derivatization and analysis corresponds to 3 micrograms of SAP per filter (assuming an esterification factor of 0.30 microgram of ethanol per microgram of SAP). PMID:11070542

  4. Matrix tablets based on thiolated poly(acrylic acid): pH-dependent variation in disintegration and mucoadhesion.

    Science.gov (United States)

    Guggi, Davide; Marschütz, Michaela K; Bernkop-Schnürch, Andreas

    2004-04-15

    This study examined the influence of the pH on the mucoadhesive and cohesive properties of polyarcylic acid (PAA) and thiolated PAA. The pH of PAA (molecular mass: 450 kDa) and of a corresponding PAA-cysteine conjugate was adjusted to 3, 4, 5, 6, 7 and 8. The amount of immobilised thiol groups and disulfide bonds was determined via Ellman's reagent. Tablets were compressed out of each pH-batch of both thiolated and unmodified PAA and the swelling behaviour, the disintegration time and the mucoadhesiveness were evaluated. The amount of thiol/disulfide groups per gram thiolated PAA of pH 3 and pH 8 was determined to be 332 +/- 94 micromol and 162 +/- 46 micromol, respectively. The thiolated PAA tablets displayed a minimum four-fold higher water uptake compared to unmodified PAA tablets. A faster and higher water uptake of both polymer types was observed above pH 5. Thiolated polymer tablets showed a 3-20-fold more prolonged disintegration time than unmodified PAA tablets. The cohesiveness of PAA-cysteine conjugate increased at higher pH, whereas the unmodified PAA behaved inversely. A 3-7-fold stronger mucoadhesiveness was observed for the PAA-cysteine conjugate tablets compared to unmodified PAA tablets. For both thiolated and unmodified polymer the mucoadhesiveness was 2-4-fold enhanced below pH 5. The difference in mucoadhesion between the two polymer types was most pronounced at these lower pH values. In this study substantial information regarding the pH-dependence of mucoadhesion and cohesion of unmodified polyacrylates and of thiolated polyacrylates is provided, representing helpful basic information for an ameliorated deployment of these polymers. PMID:15072786

  5. A approximate non-isothermal method to study kinetic processes controlled by a distribution of rate constants: the case of a photochromic azobenzene derivative dissolved in a polymer matrix

    Czech Academy of Sciences Publication Activity Database

    Janus, K.; Koshets, I. A.; Sworakowski, J.; Nešpůrek, Stanislav

    2002-01-01

    Roč. 12, č. 6 (2002), s. 1657-1663. ISSN 0959-9428 R&D Projects: GA AV ČR IAA1050901; GA ČR GA202/01/0518 Institutional research plan: CEZ:AV0Z4050913 Keywords : photochromism * bleaching kinetics * azobenzene Subject RIV: BG - Nuclear, Atomic and Molecular Physics, Colliders Impact factor: 2.683, year: 2002

  6. Mesoporous polyacrylic acid supported silver nanoparticles as an efficient catalyst for reductive coupling of nitrobenzenes and alcohols using glycerol as hydrogen source.

    Science.gov (United States)

    Mandi, Usha; Roy, Anupam Singha; Kundu, Sudipta K; Roy, Susmita; Bhaumik, Asim; Islam, Sk Manirul

    2016-06-15

    Silver nanoparticle immobilized mesoporous cross-linked polyacrylic acid (Ag-MCP-1) has been synthesized via aqueous-phase polymerization of acrylic acid followed by the surface immobilization with silver nanoparticles. The nanocomposite material has been characterized by different spectroscopic techniques. Powder X-ray diffraction patterns revealed the formation of silver nanoparticles, while transmission electron microscope image showed that Ag nanoparticles are formed and uniformly dispersed in the mesoporous polyacrylic acid. The Ag-MCP-1 nanocomposite can be used as an efficient heterogeneous catalyst in the reductive coupling of nitrobenzenes and alcohols using glycerol as hydrogen source. This nanocomposite can be reused more than five times without any significant decrease in its catalytic activity. PMID:27038284

  7. Influence of He/O{sub 2} atmospheric pressure plasma jet treatment on subsequent wet desizing of polyacrylate on PET fabrics

    Energy Technology Data Exchange (ETDEWEB)

    Li Xuming [Key Laboratory of Textile Science and Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); College of Textile and Clothing, Shaoxing University, Shaoxing 312000 (China); Lin Jun [Key Laboratory of Textile Science and Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Qiu Yiping, E-mail: ypqiu@dhu.edu.cn [Key Laboratory of Textile Science and Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China)

    2012-01-15

    The influence of He/O{sub 2} atmospheric pressure plasma jet (APPJ) treatment on subsequent wet desizing of polyacrylate on PET fabrics was studied in the present paper. Weight loss results indicated that the weight loss increased with an increase of plasma treatment time. Atomic force microscopy (AFM) and scanning electron microscopy (SEM) showed an increased surface roughness after the plasma treatment. SEM also showed that the fiber surfaces were as clean as unsized fibers after 35 s treatment followed by NaHCO{sub 3} desizing. X-ray photoelectron spectroscopy (XPS) analysis indicated that oxygen-based functional groups increased for the plasma treated polyacrylate sized fabrics. The percent desizing ratio (PDR) results showed that more than 99% PDR was achieved after 65 s plasma treatment followed by a 5 min NaHCO{sub 3} desizing. Compared to conventional wet desizing, indicating that plasma treatment could significantly reduce desizing time.

  8. Amendment of an acid mine soil with compost and polyacrylate polymers enhances enzymatic activities but may change the distribution of plant species

    OpenAIRE

    de Varennes, Amarilis; Queda, Cristina Cunha; Guiwei, Qu

    2009-01-01

    Many soils derived from pyrite mines spoils are acidic, poor in organic matter and plant nutrients, contaminated with trace elements, and support only sparse vegetation. The establishment of a plant cover is essential to decrease erosion and the contamination of water bodies with acid drainage containing large concentrations of trace elements. We tested the application of compost and polyacrylate polymers to promote the growth of indigenous plant species present in the mine area. Soil t...

  9. Effect of the Spacer and Aliphatic Tail Length on the Conformation of “Side-on Fixed” Liquid Crystal Polyacrylates: “SANS” Experiments

    OpenAIRE

    Lecommandoux, S.; Noirez, L.; Richard, H.; Achard, M.; Strazielle, C.; Hardouin, F.

    1996-01-01

    The backbone conformation of two different “side-on fixed” liquid crystalline polyacrylates is studied by Small Angle Neutron Scattering experiments in the nematic phase. We observe the influence of a very large spacer and a large aliphatic extremities length on the prolate anisotropy of the polymer backbone. In both situations we find a strong decrease in the conformation anisotropy of the main chain.

  10. Influence of hydrogels initial state on their ?lectrochemical and volume-gravimetric properties ?n intergel system polyacrylic acid hydrogel ?nd poly-4-vinylpyridine hydrogel

    OpenAIRE

    Jumadilov, T.; Abilov, Zh.; Kondaurov, R.; Himersen, H.; Yeskalieva, G.; Akylbekova, M.; Akimov, A.

    2015-01-01

    Electrochemical properties of intergel system polyacrylic acid (gPAA) and poly-4-vinylpyridine hydrogels (gP4VP) and conformational properties of initial hydrogels were studied depending on hydrogels initial state. Maximum activation area is: for dry hydrogels ? gPAA:gP4VP ratios 5:1 and 1:5, for swollen ? ratios 5:1, 2:4 and 1:5. ?????????? ?????????????? ??????????? ???????????? ??????? ????????? ????????????? ??????? (????) ? ???? ????-4-????????????? (??4??) ?? ????????????? ???????...

  11. Historical Cohort Study on the Factors Affecting Blood Pressure in Workers of Polyacryl Iran Corporation Using Bayesian Multilevel Modeling with Skew T Distribution

    OpenAIRE

    Gholami Fesharaki, Mohammad; Kazemnejad, Anoshirvan; Zayeri, Farid; Sanati, Javad; Akbari, Hamed

    2013-01-01

    Background Hypertension is considered as a major public health problem in most countries due to its association with ischemic heart disease which causes cerebrovascular disease and death. Objectives The purpose of the present study was to study factors affecting Blood Pressure (BP). Patients and Methods The data were extracted from annual observation of the workers who worked in Polyacryl Iran Corporation (PIC) between 1998 and 2010. In this research, we assessed the effect of Body Mass Index...

  12. Administration of intrapulmonary sodium polyacrylate to induce lung injury for the development of a porcine model of early acute respiratory distress syndrome

    OpenAIRE

    Henderson, William R.; Barnbrook, Julian; Dominelli, Paolo B.; Griesdale, Donald EG; Arndt, Tara; Molgat-Seon, Yannick; Foster, Glen; Ackland, Gareth L; Xu, James; Ayas, Najib T.; Sheel, Andrew W.

    2014-01-01

    Background The loss of alveolar epithelial and endothelial integrity is a central component in acute respiratory distress syndrome (ARDS); however, experimental models investigating the mechanisms of epithelial injury are lacking. The purpose of the present study was to design and develop an experimental porcine model of ARDS by inducing lung injury with intrapulmonary administration of sodium polyacrylate (SPA). Methods The present study was performed at the Centre for Comparative Medicine, ...

  13. Scientific Opinion on the safety evaluation of the active substance, polyacrylic acid, sodium salt, crosslinked, for use in active food contact materials

    Directory of Open Access Journals (Sweden)

    EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF

    2013-02-01

    Full Text Available This scientific opinion of CEF Panel deals with the risk assessment of polyacrylic acid, sodium salt crosslinked, FCM substance No 1015, which is intended to be used as liquid absorber in the packaging of fresh or frozen meat, poultry, and fish as well as fresh fruits and vegetables. Specific migration tests were not performed due to the high absorption of liquids by the substance. The Panel noted that if polyacrylic acid, sodium salt, crosslinked is used not in direct contact with food placed in a pad under conditions where its absorption capacity is not exceeded, then no migration is to be expected and therefore no exposure to the substance from the consumption of the packed food is expected. The CEF Panel concluded that the use of the substance polyacrylic acid, sodium salt, crosslinked does not raise a safety concern when used in absorbent pads in the packaging of fresh or frozen meat, poultry, and fish as well as fresh fruits and vegetables. The absorbent pads must be used only under conditions in which the absorption capacity of the active substance is not exceeded and direct contact with food is excluded.

  14. Scientific Opinion on safety assessment of the active substance, polyacrylic acid, sodium salt, crosslinked, for use in active food contact materials

    Directory of Open Access Journals (Sweden)

    EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF

    2014-05-01

    Full Text Available This scientific opinion of the EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids deals with the safety assessment of the polyacrylic acid, sodium salt, crosslinked, FCM substance No 1015, which is intended to be used as a liquid absorber in the packaging of fresh or frozen foods such as meat, poultry, and seafood as well as fresh fruits and vegetables. Specific migration tests were not performed due to the high absorption of liquids by the substance. The Panel noted that if polyacrylic acid, sodium salt, crosslinked, is used not in direct contact with food placed in a pad under conditions where its absorption capacity is not exceeded, then no migration is to be expected and therefore no exposure from the consumption of the packed food is expected. The Panel also considered that non-crosslinked polymer and the crosslinker do not raise a concern for genotoxicity. The CEF Panel concluded that the use of the substance polyacrylic acid, sodium salt, crosslinked, does not raise a safety concern when used in absorbent pads in the packaging of fresh or frozen meat foods poultry, and seafood as well as fresh fruits and vegetables. The absorbent pads must be used only under conditions in which the liquid absorption capacity is not exceeded and direct contact between the substance and the food is excluded.

  15. Scientific Opinion on safety assessment of the active substance, polyacrylic acid, sodium salt crosslinked, for use in active food contact materials

    Directory of Open Access Journals (Sweden)

    EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF

    2014-07-01

    Full Text Available This scientific opinion of the EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids deals with the safety assessment of polyacrylic acid, sodium salt, crosslinked, FCM substance No 1015, which is intended to be used as a liquid absorber in the packaging of fresh or frozen foods such as meat, poultry, and seafood as well as fresh fruits and vegetables. Specific migration tests were not performed due to the high absorption of liquids by the substance. The Panel noted that if polyacrylic acid, sodium salt, crosslinked is used not in direct contact with food and placed in a pad under conditions where its absorption capacity is not exceeded, then no migration is to be expected and therefore no exposure from the consumption of the packed food is expected. The Panel also considered that non-crosslinked polymer and the crosslinkers do not raise a concern for genotoxicity. The CEF Panel concluded that the use of the substance polyacrylic acid, sodium salt, crosslinked, does not raise a safety concern when used in absorbent pads in the packaging of fresh or frozen foods. The absorbent pads must be used only under conditions in which the absorption capacity of the active substance is not exceeded and direct contact with food is excluded.

  16. Study on Synthesis of Low-middle Molecular Weight Polyacrylate Sodium%中低分子量聚丙烯酸钠的合成研究

    Institute of Scientific and Technical Information of China (English)

    胡长安; 周建飞; 兰云军

    2013-01-01

      以空气-亚硫酸氢钠为引发体系,采用自由基水溶液聚合方法,实现在较低温度下制备中低分子量聚丙烯酸钠。通过正交试验研究了反应条件对聚丙烯酸钠分子量及单体转化率的影响。实验结果表明,通过控制反应条件可以合成中低分子量(5000-20000)的聚丙烯酸钠。%  The low-middle molecular weight polyacrylate sodium has been synthesized with air-sodium bisulfite as initiation system at low temperature by free radical solution polymerization. It was studied through orthogonal experiments that reaction conditions effected the molecular weight of polyacrylate sodium and the conversion ratio of monomer. The experiment results showed that the molecular weight of polyacrylate sodium was 5000~20000 under the different reaction conditions.

  17. 含氟丙烯酸酯拒水剂的制备%Synthesis of fluorine containing polyacrylate water repellent

    Institute of Scientific and Technical Information of China (English)

    赵振; 樊增禄; 李庆

    2012-01-01

    Fluorine containing polyacrylate water repellent was prepared using styrene (SM), isooctyl acry-late (2-EHA), hexafluorobutyl methacrylate (Actyflon-G04) as the monomers with semi-continuous seed emulsion polymerization method. The optimal synthesis process of fluorine containing polyacrylate water repellent was analyzed. The prepared copolymer was characterized by Fourier transform infrared spectroscopy, and was applied in cotton fabric. The results showed that the optimum synthesis condition was: 3:2 of SM and 2-EHA mass ratio, 50% of Actyflon-G04 on the total mass of monomers, 2.5% of emulsifier on the total mass of monomers, 0.8% of initiator on the total mass of monomers, 80 ℃ of polymerization temperature, 1.5 h of holding time. And the synthetic copolymers was applied in cotton fabric, the water contact angle was up to 136.5°, with good water repellency.%以苯乙烯(SM)、丙烯酸异辛酯(2-EHA)与甲基丙烯酸十二氟庚酯(Actyflon-G04)为反应单体,采用半连续种子乳液聚合方式,制备了含氟丙烯酸酯拒水剂.分析了含氟丙烯酸酯拒水剂的最佳合成工艺,对制备的共聚物进行傅立叶转换红外光谱表征,并将其处理到棉织物上.最佳合成工艺为∶m(SM)∶m(2-EHA)=3∶2,Actyflon-G04 50%(对单体总质量),乳化剂2.5%(对单体总质量),引发剂0.8%(对单体总质量),聚合反应温度为80℃,保温时间为1.5 h.将合成的共聚物处理到棉织物上,整理后织物对水的接触角可达136.5°,具有良好的拒水性能.

  18. 含偶氮苯结构聚酯的合成及性能%Synthesis and propertiesof polyesters containing azobenzene unit

    Institute of Scientific and Technical Information of China (English)

    于世钧; 高博; 王璐; 王红; 高永久

    2011-01-01

    Three novel linear polyesters(P1~P3) containing azobenzene unit are synthesized by condensation polymerization of diethyl 5-(4-alkoxy phenylazo) isophthalate and different glycols(l,3-propyl-ene glycol, 1,6-hexylene glycol, polyethylene glycol-400). The structure and properties of the polyes-ters(Pl~P3) are confirmed by IR, UV-vis, 'H NMR, SEC and TG-DTA. Polyesters(Pl~P3) containing azobenzene unit dissolve in common organic solvents such as tetrahydrofuran and chloroform, et al The intrinsic viscosities of polyesters(Pl~P3) in chloroform are 0. 514 6, 0. 463 9,0. 565 7 dL/g, the Mw are 39 200,34 983,45 507 g/mol, 5% weight loss temperature of polyesters(P1~P3) are 287,276,335 V. Polyesters(P1~P3) take place trans-cis photoisomerization under 365 run UV irradiation. With the ultraviolet excitation at 350 nm, polyesters(Pl~P3) emit purple fluorescence at 398 nm.%以间苯二甲酸为原料合成了5-[4-(乙氧基)苯基偶氮]-1,3-苯二甲酸二乙酯,分别与1,3-丙二醇、1,6-己二醇和聚乙二醇-400熔融聚合得到了3种新型含有偶氮苯结构的线型聚酯(P1~P3),采用IR、UV-vis、1H NMR、SEC和TG-DTA等对聚酯结构和性能进行了表征.聚酯(P1~P3)易溶于THF、CHCl3等有机溶剂,特性黏度分别为0.514 6、0.463 9、0.565 7 dL/g,Mw分别为39 200、34 983、45 507 g/mol,5%失重温度分别为287、276、335℃.在365 nm紫外光照射下,聚酯(P1~P3)中偶氮苯结构发生反-顺异构化,在350 nm波长光激发下,聚酯(P1~P3)在398 nm附近发紫色光.

  19. Capture of Tumor Cells on Anti-EpCAM-Functionalized Poly(acrylic acid)-Coated Surfaces.

    Science.gov (United States)

    Andree, Kiki C; Barradas, Ana M C; Nguyen, Ai T; Mentink, Anouk; Stojanovic, Ivan; Baggerman, Jacob; van Dalum, Joost; van Rijn, Cees J M; Terstappen, Leon W M M

    2016-06-15

    The presence of tumor cells in blood is predictive of short survival in several cancers and their isolation and characterization can guide toward the use of more effective treatments. These circulating tumor cells (CTC) are, however, extremely rare and require a technology that is sufficiently sensitive and specific to identify CTC against a background of billions of blood cells. Immuno-capture of cells expressing the epithelial cell adhesion molecule (EpCAM) are frequently used to enrich CTC from blood. The choice of bio conjugation strategy and antibody clone is crucial for adequate cell capture but is poorly understood. In this study, we determined the binding affinity constants and epitope binding of the EpCAM antibodies VU1D-9, HO-3, EpAb3-5, and MJ-37 by surface plasmon resonance imaging (SPRi). Glass surfaces were coated using a poly(acrylic acid) based coating and functionalized with anti-EpCAM antibodies. Binding of cells from the breast carcinoma cell line (SKBR-3) to the functionalized surfaces were compared. Although EpAb3-5 displayed the highest binding affinity HO-3 captured the highest amount of cells. Hence we report differences in the performance of the different antibodies and more importantly that the choice of antibody to capture CTC should be based on multiple assays. PMID:27187784

  20. Gamma radiation synthesis of comb-type graft hydrogels based on poly(acrylic acid) and 4-vinylpyridine

    International Nuclear Information System (INIS)

    A pH-sensitive comb-type hydrogel was obtained by gamma radiation polymerization and crosslinking of acrylic acid (AAc) in solution. The pH-sensitive 4-vinylpyridine (4VP) was then grafted to the poly acrylic acid (PAAc) hydrogel using gamma radiation from a 60Co source. The comb type graft polymers obtained (net-PAAc)-g-4VP has been studied through determination of graft yield and swelling behavior. The critical pH value was found to be 5.6. The apparent mechanical properties appear to be qualitatively better than hydrogels of PAAc upon swelling. The new comb-type system presents faster swelling response (30 h) than the polyacrylic acid hydrogel (50 h). The increase in dose rate from 7.3 to 11.3 kGy h-1, increase the radiation grafting percentage of 4VP in the system. Comb-type polymers were also characterized by DSC, TGA and FTIR-ATR. (author)