WorldWideScience

Sample records for butylenes

  1. Poly(butylene succinate-co-butylene adipate)/cellulose nanocrystal composites modified with phthalic anhydride.

    Science.gov (United States)

    Zhang, Xuzhen; Zhang, Yong

    2015-12-10

    As a kind of biomass nanofiller for polymers, cellulose nanocrystal (CNC) has good mechanical properties and reinforcing capability. To improve the compatibility of poly(butylene succinate-co-butylene adipate) (PBSA)/CNC composites, phthalic anhydride was used as a compatilizer during melt mixing, leading to the significant improvement of the mechanical properties and thermal stability of the composites, which is related to the better dispersion of CNC in the composites. The addition of phthalic anhydride could accelerate the crystallization of PBSA component as evidenced by the curves of isothermal crystallization of the composites, but had little effect on the crystalline polymorphs of PBSA component. The addition of phthalic anhydride could strongly improve the hydrophobicity of the composites. The good mechanical properties, fast crystallization and improved hydrophobicity of PBSA/CNC composites with phthalic anhydride are favor to their practical commercial utilization.

  2. Design, Synthesis and Characterisation of Novel Biodegradable Aliphatic Copolyesters- Poly(ethylene sebacate-co-butylene succinate and Poly(ethylene sebacate-co-butylene adipate

    Directory of Open Access Journals (Sweden)

    L. SOWBAGYALAKSHMI PRABHA

    2012-12-01

    Full Text Available Synthesis of novel aliphatic biodegradable copolyesters namely Poly (ethylene sebacate-co-butylene succinate and Poly (ethylene sebacate-co-butylene adipate were carried out using Poly (butylene Succinate, Poly (Butylene Adipate and Poly (Ethylene Sebacate in presence of Poly Phosphoric acid. Synthesis of Poly (Butylene Succinate, Poly (Butylene Adipate and Poly (Ethylene Sebacate were carried out using respective diols and diacids in presence of titanium tetrabutoxide as catalyst. Newly synthesized copolyesters were characterized by solubility studies, viscosity measurements, thermal analysis, IR Spectroscopy and Nuclear Magnetic Resonance Spectroscopy (1H-NMR and 13C-NMR. The characteristic peaks present in the homopolyesters were recorded in the copolymers as well. DSC analysis of the copolyesters showed multiple melting peaks, while increase of methylene units in the di-acid decreased the Tg.

  3. Amide-modified poly(butylene terephthalate): polycondensation

    NARCIS (Netherlands)

    Bennekom, van A.C.M.; Gaymans, R.J.

    1996-01-01

    The synthesis of poly(ester amide) copolymers (PBTA) based on poly(butylene terephthalate) (PBT) and nylon-4,T with the diamide of butanediamine and dimethyl terephthelate (N,N′-bis(p-carbomethoxybenzoyl)butanediamine) has been carried out. Different melt and solid state condensation reactors were u

  4. Effect of organo-modified montmorillonite on poly(butylene succinate/poly(butylene adipate-co-terephthalate nanocomposites

    Directory of Open Access Journals (Sweden)

    2010-07-01

    Full Text Available The composite material based on poly(butylene succinate (PBS, poly(butylene adipate-co-terephthalate (PBAT and organo-modified montmorillonite (OMMT were prepared by melt blending technique and characterized. Sodium montmorillonite (Na-MMT was successfully modified by octadecylammonium (ODA and dimethyldioctadecylammonium (DDOA salts to become OMMT through cation exchange technique which is shown by the increase of basal spacing of clay by XRD. The addition of the OMMT to the PBS/PBAT blends produced nanocomposites which is proved by XRD and TEM. Tensile tests showed increase in tensile strength and modulus which is attributed to the existence of strong interactions between PBS/PBAT and clay, particularly with OMMT. Highest tensile strength of nanocomposite was observed at 1 wt% of OMMT incorporated. TGA study showed that the thermal stability of the blend increased after the addition of clays. SEM micrographs of the fracture surfaces show that the morphology of the blend becomes homogeneous and smoother with presence of OMMT.

  5. COMPOSITIONAL HETEROGENEITY OF ETHYLENE OXIDE-BUTYLENE TEREPHTHALATE SEGMENTED COPOLYMER

    Institute of Scientific and Technical Information of China (English)

    De-zhu Ma; Dong-sheng Li; Ming-chuan Zhao; Mo-zhen Wang; Ran Ye; Xiao-lie Luo

    1999-01-01

    A series of ethylene oxide-butylene terephthalate (EOBT) segmented copolymers with different soft segment length and hard segment content were synthesized. The compositional heterogeneity was studied by solvent extraction. The results show that the compositional heterogeneity increases when soft segment length and hard segment content increase. The compositional heterogeneity is also reflected in the crystallization behavior and morphology of soft and hard segment in EOBT segmented copolymer. The more compositional heterogeneous the EOBT segmented copolymer is, the more different the morphology and the crystallization behavior between separated fractions. Compared with ethylene oxide-ethylene terephthalate (EOET) segmented copolymer, compositional heterogeneity in EOBT segmented copolymer is weaker. But the compositional heterogeneity in EOBT segmented copolymer with long soft segment and high hard segment content is still obvious.

  6. Synthesis by ATRP of poly(ethylene-co-butylene)-block-polystyrene, poly(ethylene-co-butylene)-block-poly(4-acetoxystyrene) and its hydrolysis product poly(ethylene-co-butylene)-block-poly(hydroxystyrene)

    DEFF Research Database (Denmark)

    Jankova, Katja; Kops, Jørgen; Chen, Xianyi;

    1999-01-01

    Diblock copolymers of poly(ethylene-co-butylene) and polystyrene or poly(4-acetoxystyrene) are synthesized by atom transfer radical polymerization (ATRP) using a 2-bromopropionic ester macroinitiator prepared from commercial monohydroxyl functional narrow dispersity hydrogenated polybutadiene...... copolymer with poly(4-acetoxystyrene) was hydrolyzed to the corresponding poly(4-hydroxystyrene) sequence....

  7. Data on synthesis of oligomeric and polymeric poly(butylene adipate-co-butylene terephthalate model substrates for the investigation of enzymatic hydrolysis

    Directory of Open Access Journals (Sweden)

    Veronika Perz

    2016-06-01

    Full Text Available The aliphatic-aromatic copolyester poly(butylene adipate-co-butylene terephthalate (PBAT, also known as ecoflex, contains adipic acid, 1,4-butanediol and terephthalic acid and is proven to be compostable [1–3]. We describe here data for the synthesis and analysis of poly(butylene adipate-co-butylene terephthalate variants with different adipic acid:terephatalic acid ratios and 6 oligomeric PBAT model substrates. Data for the synthesis of the following oligomeric model substrates are described: mono(4-hydroxybutyl terephthalate (BTa, bis(4-(hexanoyloxybutyl terephthalate (HaBTaBHa, bis(4-(decanoyloxybutyl terephthalate (DaBTaBDa, bis(4-(tetradecanoyloxybutyl terephthalate (TdaBTaBTda, bis(4-hydroxyhexyl terephthalate (HTaH and bis(4-(benzoyloxybutyl terephthalate (BaBTaBBa. Polymeric PBAT variants were synthesized with adipic acid:terephatalic acid ratios of 100:0, 90:10, 80:20, 70:30, 60:40 and 50:50. These polymeric and oligomeric substances were used as ecoflex model substrates in enzymatic hydrolysis experiments in the article “Substrate specificities of cutinases on aliphatic-aromatic polyesters and on their model substrates” [4].

  8. Organoclay nanocomposites of post-industrial waste poly(butylene terephthalate) from automotive parts.

    Science.gov (United States)

    Quispe, Noe B; Fernandes, Elizabeth G; Zanata, Fernanda; Bartoli, Julio R; Souza, Diego H S; Ito, Edson N

    2015-10-01

    Polymeric nanocomposites are novel materials of huge interest owing to their favourable cost/performance ratio with low amount of nanofillers, improved thermal resistance, flame retardancy and mechanical properties in relation to their matrices. In this work, composites based on post-industrial waste or primary recycled poly(butylene terephthalate) and 5 wt.% of organic modified montmorillonite clays were melt compounded using a twin-screw extruder. A 2(2) factorial experimental design was used to study the compounding and processing variables: Organic modified montmorillonite with one or two hydrogenated tallow (initial basal spacing) and screw speed of the extruder. X-ray diffraction and transmission electron microscopy suggest that a partial exfoliation of the organoclay in the recycled poly(butylene terephthalate) matrix was achieved for organic modified montmorillonite with lower initial basal spacing. On the other hand, formulations containing organic modified montmorillonite with higher initial basal spacing showed only intercalated structure. The recycled poly(butylene terephthalate)-organic modified montmorillonite nanocomposites did not drip flaming material during burning tests. Storage of dynamic-mechanical, tensile and flexural moduli of the recycled poly(butylene terephthalate)-organic modified montmorillonite were improved when compared with both virgin and recycled poly(butylene terephthalate)s, mainly for nanocomposites formulated at a lower initial basal spacing organoclay. This could be related to a better diffusion of polymer into organic modified montmorillonite layers compared with the higher initial basal spacing organoclay. The improvements on the physical properties of recycled poly(butylene terephthalate) showed the feasibility to add value to primary recycled engineering thermoplastics with a very small amount of organic modified montmorillonite. PMID:26341637

  9. Organoclay nanocomposites of post-industrial waste poly(butylene terephthalate) from automotive parts.

    Science.gov (United States)

    Quispe, Noe B; Fernandes, Elizabeth G; Zanata, Fernanda; Bartoli, Julio R; Souza, Diego H S; Ito, Edson N

    2015-10-01

    Polymeric nanocomposites are novel materials of huge interest owing to their favourable cost/performance ratio with low amount of nanofillers, improved thermal resistance, flame retardancy and mechanical properties in relation to their matrices. In this work, composites based on post-industrial waste or primary recycled poly(butylene terephthalate) and 5 wt.% of organic modified montmorillonite clays were melt compounded using a twin-screw extruder. A 2(2) factorial experimental design was used to study the compounding and processing variables: Organic modified montmorillonite with one or two hydrogenated tallow (initial basal spacing) and screw speed of the extruder. X-ray diffraction and transmission electron microscopy suggest that a partial exfoliation of the organoclay in the recycled poly(butylene terephthalate) matrix was achieved for organic modified montmorillonite with lower initial basal spacing. On the other hand, formulations containing organic modified montmorillonite with higher initial basal spacing showed only intercalated structure. The recycled poly(butylene terephthalate)-organic modified montmorillonite nanocomposites did not drip flaming material during burning tests. Storage of dynamic-mechanical, tensile and flexural moduli of the recycled poly(butylene terephthalate)-organic modified montmorillonite were improved when compared with both virgin and recycled poly(butylene terephthalate)s, mainly for nanocomposites formulated at a lower initial basal spacing organoclay. This could be related to a better diffusion of polymer into organic modified montmorillonite layers compared with the higher initial basal spacing organoclay. The improvements on the physical properties of recycled poly(butylene terephthalate) showed the feasibility to add value to primary recycled engineering thermoplastics with a very small amount of organic modified montmorillonite.

  10. Amorphous/crystal and polymer/filler interphases in biocomposites from poly(butylene succinate)

    Energy Technology Data Exchange (ETDEWEB)

    Signori, Francesca [Consiglio Nazionale delle Ricerche - Istituto per i Processi Chimico-Fisici (CNR-IPCF), Via G. Moruzzi 1, I-56124 Pisa (Italy); Pelagaggi, Martina [Universita di Pisa - Dipartimento di Chimica e Chimica Industriale, Via Risorgimento 35, I-56126 Pisa (Italy); Bronco, Simona [Consiglio Nazionale delle Ricerche - Istituto per i Processi Chimico-Fisici (CNR-IPCF), Via G. Moruzzi 1, I-56124 Pisa (Italy); Righetti, Maria Cristina, E-mail: righetti@ipcf.cnr.it [Consiglio Nazionale delle Ricerche - Istituto per i Processi Chimico-Fisici (CNR-IPCF), Via G. Moruzzi 1, I-56124 Pisa (Italy)

    2012-09-10

    Highlights: Black-Right-Pointing-Pointer The existence of intermolecular interactions between poly(butylene succinate) and hemp fibres was proved from specific heat capacities data. Black-Right-Pointing-Pointer Different degrees of mobility of the poly(butylene succinate) amorphous segments were evidenced at the amorphous/crystal interphase. Black-Right-Pointing-Pointer Devitrification of the rigid amorphous fraction in poly(butylene succinate) was found to occur before and simultaneously with the fusion. - Abstract: Poly(butylene succinate)-hemp composites (PBS-hemp), with hemp content in the range 0-40 wt.%, were prepared in the melt and characterized. This paper focuses on the detailed analysis of the thermal behaviour of the PBS-hemp composites, investigated by differential scanning calorimetry (DSC), to enlighten the polymer/fibre interphase features. The occurrence of specific intermolecular interactions between PBS and hemp was assessed from specific heat capacity data. Different degrees of mobility of the PBS amorphous segments were found at the amorphous/crystal interphases. A broadening of the bulk glass transition was observed, and attributed to the presence of polymer segments slightly constrained. Moreover, a rigid amorphous fraction that devitrifies at temperatures higher than the bulk glass transition, partly before the melting region and partly simultaneously with the fusion, was observed and quantified, and attributed to the presence of major constraints probably occurring in geometrically restricted areas.

  11. Crystallization of poly(ethylene terephthalate) and poly (butylene terephthalate) modified by diamides

    NARCIS (Netherlands)

    Bouma, Krista; Gaymans, Reinoud J.

    2001-01-01

    Poly(ethylene terephthalate) (PET) and poly (butylene terephthalate) have been modified by diamide units (0.1-1 mol%) in an extrusion process and the crystallization behavior studied. The diamides used were: for PET, T2T-dimethyl (N, N-bis(p-carbomethoxybenzoyl)ethanediamine) and for PBT, T4T-dimeth

  12. Water vapor and gas transport through a poly (butylene terephthalate) poly (ethylene oxide) block copolymer

    NARCIS (Netherlands)

    Metz, S.J.; Potreck, J.; Mulder, M.H.V.; Wessling, M.

    2002-01-01

    In this paper the transport behavior of water vapor and nitrogen in a poly(butylene terephthalate) poly (ethylene oxide) block copolymer is discussed. This polymer has a high solubility for water (300 cm3 (STP)/cm3 polymer at activity 0.9). A new permeation set up has been built to determine the wat

  13. Electrospun Nanoporous Poly(butylenes succinate-co-bytylene terephthalate Nonwoven Mats

    Directory of Open Access Journals (Sweden)

    Liang Wang

    2011-01-01

    Full Text Available A traditional Chinese drug “Yunnan Baiyao” is used as an additive in poly(butylenes succinate-co-bytylene terephthalate (PBST solution, which is a kind of biodegradable aliphatic-aromatic copolyesters, to produce microspheres with nanoporosity by electrospinning; the tunable size of nanoporosity can be controlled by changing the voltage applied in the electrospinning process.

  14. Poly(ethylene-co-butylene) functionalized multi walled carbon nanotubes applied in polypropylene nanocomposites

    DEFF Research Database (Denmark)

    Daugaard, Anders Egede; Jankova Atanasova, Katja; Marín, Jose Manuel Roman;

    2012-01-01

    A novel functionalized multi walled carbon nanotube (MWCNT) was prepared through grafting with α-azido-poly(ethylene-co-butylene) (PEB-N3). The PEB-N3 was prepared through a two step procedure and grafted onto an industrial grade multi walled carbon nanotube (MWCNT) through a highly efficient...

  15. Biodegradation of poly(lactic acid), poly(hydroxybutyrate-co-hydroxyvalerate), poly(butylene succinate) and poly(butylene adipate-co-terephthalate) under anaerobic and oxygen limited thermophilic conditions

    OpenAIRE

    Jutakan Boonmee; Charnwit Kositanont; Thanawadee Leejarkpai

    2016-01-01

    In order to study the biodegradation behavior of biodegradable plastics in landfill conditions, four types of biodegradable plastics including poly(lactic acid) (PLA), poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV), poly(butylene succinate) (PBS), and poly(butylene adipate-co-terephthalate) (PBAT) were tested by burying in sludge mixed soil medium under anaerobic and oxygen limited conditions. The experiments were operated at 52 ± 2ºC in dark conditions according to ISO15985. The degree of b...

  16. Synthesis and properties of novel aliphatic polycarbonate from carbon dioxide with 1,2-butylene oxide and ε-caprolactone

    Institute of Scientific and Technical Information of China (English)

    Yan Fei Liu; Ke Long Huang; Dong Ming Peng; Su Qin Liu; Hong Wu

    2007-01-01

    A new degradable aliphatic poly(butylene-co-ε-caprolactone carbonate) (PBCL) was synthesized through the terpolymerization of carbon dioxide, 1,2-butylene oxide (BO) and ε-caprolactone (CL), a polymer supported bimetallic complex (PBM) was used as a catalyst. The terpolymers prepared were characterized by FT-IR, 1H NMR, 13C NMR, WXRD and DSC. The hydrolysis tests were carried out to appraise the degradability of the copolymers.

  17. Production of 2,3-butylene glycol from citrus wastes. II. The Bacillus polymyxa fermentation.

    Science.gov (United States)

    Long, S K; Patrick, R

    1965-11-01

    The conditions required for production of levo 2,3-butylene glycol by Bacillus polymyxa from citrus molasses were studied. Starter cultures required acclimatization to the substrate prior to inoculation of the fermentation medium. Maximal production of butylene glycol with minimal residual sugar was obtained with a medium consisting of molasses, diluted to 20 degrees Brix, and 0.4% urea. Optimal environmental conditions included aeration at 0.11 volumes of air per volume of medium per minute, maintenance of pH at 6.0 to 6.2, a fermentation temperature of 30 C, and a stirring rate of 420 rev/min. The concentration of butylene glycol obtained in the fermentation beer ranged from 2.3 to 4.4%. The optical rotation of the glycol ranged from [alpha](D) (23 degrees ) = -1.01 degrees to -10.45 degrees . The variation in rotation was probably due to the presence of contaminating substances in the distillate. PMID:5866043

  18. Reactive processing of maleic anhydride-grafted poly(butylene succinate and the compatibilizing effect on poly(butylene succinate nanocomposites

    Directory of Open Access Journals (Sweden)

    Z. A. Mohd Ishak

    2013-04-01

    Full Text Available In this study, maleic anhydride-grafted poly(butylene succinate (PBS-g-MA was synthesized via reactive meltgrafting process using different initiator contents. The grafting efficiency was increased with the initiator content, manifested by the higher degree of grafting in PBS-g-MA. The grafting reaction was confirmed through Fourier transform infrared (FTIR spectroscopy and nuclear magnetic resonance (NMR spectroscopy. Then, PBS-g-MA was incorporated into organo-montmorillonite (OMMT filled poly(butylene succinate (PBS nanocomposites as compatibilizer. Mechanical properties of PBS nanocomposites were enhanced after compatibilized with PBS-g-MA, due to the better dispersion of OMMT in PBS matrix and the improved filler-matrix interfacial interactions. This was verifiable through X-ray diffraction (XRD, transmission electron microscopy (TEM and scanning electron microscopy (SEM. Differential scanning calorimetry (DSC showed that the degree of crystallinity and melting temperature increased after addition of PBS-g-MA. However, the presence of PBS-g-MA did not favor the thermal stability of the nanocomposites, as reported in the thermogravimetry (TGA.

  19. Complex self-assembly of reverse poly(butylene oxide)-poly(ethylene oxide)-poly(butylene oxide) triblock copolymers with long hydrophobic and extremely lengthy hydrophilic blocks.

    Science.gov (United States)

    Cambón, Adriana; Figueroa-Ochoa, Edgar; Juárez, Josué; Villar-Álvarez, Eva; Pardo, Alberto; Barbosa, Silvia; Soltero, J F Armando; Taboada, Pablo; Mosquera, Víctor

    2014-05-15

    Amphiphilic block copolymers have emerged during last years as a fascinating substrate material to develop micellar nanocontainers able to solubilize, protect, transport, and release under external or internal stimuli different classes of cargos to diseased cells or tissues. However, this class of materials can also induce biologically relevant actions, which complement the therapeutic activity of their cargo molecules through their mutual interactions with biologically relevant entities (cellular membranes, proteins, organelles...); these interactions at the same time, are regulated by the nature, conformation, and state of the copolymeric chains. For these reasons, in this paper we investigated the self-assembly process and physico-chemcial properties of two reverse triblock poly(butylene oxide)-poly(ethylene oxide)-poly(butylene oxide) block copolymers, BO14EO378BO14 and BO21EO385BO21, which have been recently found to be very useful as drug delivery nanovehicles and biological response modifiers under certain conditions (A. Cambón et al. Int. J. Pharm. 2013, 445, 47-57) in order to obtain a clear picture of the solution behavior of this class or block copolymers and to understand their biological activity. These block copolymers are characterized by possessing long BO blocks and extremely lengthy central EO ones, which provide them with a rich rheological behavior characterized by the formation of flowerlike micelles with sizes ranging from 20 to 40 nm in aqueous solution and the presence of intermicellar bridging even at low copolymers concentrations as denoted by atomic force microscopy. Bridging is also clearly observed by analyzing the rheological response of these block copolymers both storage and loss moduli upon changes on time, temperature, and or concentration. Strikingly, the relatively wide Poisson distribution of the polymeric chains make the present copolymers behave rather distinctly to conventional associative thickeners. The observed rich

  20. Lenghty reverse poly(butylene oxide)-poly(ethylene oxide)-poly(butylene oxide) polymeric micelles and gels for sustained release of antifungal drugs.

    Science.gov (United States)

    Figueroa-Ochoa, Edgar B; Villar-Alvarez, Eva M; Cambón, Adriana; Mistry, Dharmista; Llovo, José; Attwood, David; Barbosa, Silvia; Soltero, J F Armando; Taboada, Pablo

    2016-08-20

    In this work, we present a detailed study of the potential application of polymeric micelles and gels of four different reverse triblock poly(butylene oxide)-poly(ethylene oxide)-poly(butylene oxide) copolymers (BOnEOmBOn, where n denotes the respective block lengths), specifically BO8EO90BO8, BO14EO378BO14, BO20EO411BO20 and BO21EO385BO21, as effective drug transport nanocarriers. In particular, we tested the use of this kind of polymeric nanostructures as reservoirs for the sustained delivery of the antifungals griseofulvin and fluconazole for oral and topical administration. Polymeric micelles and gels formed by these copolymers were shown to solubilize important amounts of these two drugs and to have a good stability in physiologically relevant conditions for oral or topical administration. These polymeric micellar nanocarriers were able to release drugs in a sustained manner, being the release rate slower as the copolymer chain hydrophobicity increased. Different sustained drug release profiles were observed depending on the medium conditions. Gel nanocarriers were shown to display longer sustained release rates than micellar formulations, with the existence of a pulsatile-like release mode under certain solution conditions as a result of their inner network structure. Certain bioadhesive properties were observed for the polymeric physical gels, being moderately tuned by the length and hydrophobicity of the polymeric chains. Furthermore, polymeric gels and micelles showed activity against the yeast Candida albicans and the mould demartophytes (Trichophyton rubrum and Microsporum canis) and, thus, may be useful for the treatment of different cutaneous fungal infections. PMID:27289012

  1. THERMALLY STIMULATED SHAPE MEMORY BEHAVIOR OF (ETHYLENE OXIDE-BUTYLENE TEREPHTHALATE) SEGMENTED COPOLYMER

    Institute of Scientific and Technical Information of China (English)

    Xiao-lie Luo; Ming-chuan Zhao; Mo-zhen Wang; Lu-na Ding; De-zhu Ma

    2000-01-01

    The thermally stimulated shape memory behavior of ethylene oxide-butylene terephthalate (EOBT) segmented copolymers with different soft segment molecular weight and hard segment content was investigated. The deformation recovery ratio Rf of the EOBT samples increases with the soft segment molecular weight and the hard segment weight content, while the average overall deformation recovery speed Vr increases with the hard segment content. The temperature of maximum deformation recovery speed (TM) is determined by the melting temperature of the soft segment crystals and the stability of the crystallized hard segment domains.

  2. Alternating polyesteramides based on 1,4-butylene terephthalamide: 4. Alternating polyetheresteramides based on glycols (4NTglycol)

    NARCIS (Netherlands)

    Serrano, P.J.M.; Gaymans, R.J.

    1998-01-01

    Polyetheresteramides (PEEAs) have been synthesised in the melt from 1,4-butylene terephthalamide and ethylene or propylene glycols. The ethylene glycols were ethylenediol, diethylene glycol, triethylene glycol and tetraethylene glycol. The propylene glycols were 1,3-propanediol and the mixtures of 1

  3. Alternating polyesteramides based on 1,4-butylene terephthalamide: 2. alternating polyesteramides based on a single, linear diol (4NTm)

    NARCIS (Netherlands)

    Serrano, P.J.M.; Thuss, E.H.L.; Gaymans, R.J.

    1997-01-01

    Strictly alternating polyesteramides consisting of 1,4-butylene terephthalamide and aliphatic diols have been synthesized in the melt in the presence of a titanium catalyst. The influence of diol length on the thermal and mechanical properties was studied. Depending on its structure, the diol took p

  4. Preparation of nanocomposites based on poly(Butylene Succinate) and montmorillonite organoclay via in situ polymerization

    International Nuclear Information System (INIS)

    Nanocomposites based on poly(butylene succinate) (PBS) and organophilic montmorillonite were synthesized via in situ polymerization using three different clay compositions (4, 6 and 8 wt%). The products were characterized by several different techniques. X-ray diffraction was useful to confirm the increase of the interlayer spacing of the clay due to the presence of the polymer chains among layers. Thermal analysis indicated that the polymerization method chosen led to materials with lower thermal stability compared to the pure PBS, due to the difficulty of chain growth in the presence of the clay. Low-field NMR technique was used to assess clay dispersion in the polymer, with exfoliated structures predominating in the nanocomposites. (author)

  5. STUDIES ON EPOXY RESINS MODIFIED WITH POLY (BUTYLENE TEREPHTHALATE)-b-POLY (TETRAMETHYLENE GLYCOL)

    Institute of Scientific and Technical Information of China (English)

    WANG Xia; ZHAO Binyi; LI Zhengyi; YU Yunzhao

    1997-01-01

    Poly(butylene terephthalate)-b-poly(tetramethylene glycol) (PBT-b-PTMG) was used as rheology modifier for the epoxy resin. The segmental copolymer formed spherulites in the epoxy medium. This copolymer was very effective in endowing yield stresses to the liquid resin. The PTMG segment brought in a lowering of the dissolution temperature of the spherulites in the epoxy gel. The cured resin with PBT-b-PTMG as modifier was twophase materials. The rheology modifier improved the mechanical properties of the cured resin as well. The flexible PTMG segments, however, were not in favour of the toughening effect of the modifier. This was attributed to the large domain size of the dispersed phase.

  6. Influence of Teflon substrate on crystallization and enzymatic degradation of polymorphic poly(butylene adipate)

    DEFF Research Database (Denmark)

    Ning, Zhenbo; Nielsen, Ronnie Bo Højstrup; Zhao, Lifen;

    2014-01-01

    Oriented and non-oriented Teflon films, which were found to have the same crystalline structure, but different surface morphologies, were used to sandwich poly(butylene adipate) (PBA) films during isothermal crystallization. It was found that both the Teflon surface structure and the PBA...... polymorphic structure are the determining factors to induce epitaxial crystallization. The oriented Teflon film was able to induce epitaxial crystallization of PBA alpha crystal, while the non-oriented Teflon did not induce any epitaxial crystallization of PBA. Epitaxial crystallization did not occurred for...... PBA beta crystals between neither the oriented nor the non-oriented Teflon films. The enzymatic degradation rate of PBA films was not determined by the epitaxial crystallization, in fact it was still dependent on the polymorphic crystal structure of PBA. The morphological changes of PBA films after...

  7. Effect of coke formation on the transformations of butylenes on a high-silica zeolite catalyst

    Science.gov (United States)

    Gashimov, F. A.; Kozharov, A. I.; Nadirov, P. A.; Mirzai, J. I.

    2010-08-01

    The transformations of butylenes on a high-silica zeolite catalyst (HHSZC) at 423-773 K were studied. Liquid reaction products formed above 443 K. The liquid phase of the reaction products mainly consisted of aliphatic hydrocarbons at 448-523 K and aromatic hydrocarbons at 623-723 K. The catalyst activity in the formation of liquid products did not show itself until 4-6% consolidation products (CPs) accumulated on its surface. DTA and gravimetric studies showed that CPs were nonuniform in composition. Some of the CPs were removed by decomposition under nitrogen, while others by oxidation with oxygen. It was inferred from ammonia adsorption data that the accumulation of CPs on the surface of HHSZC led to a decrease in the number of acid centers.

  8. Poly(Butylene Terephthalate Based Composites Containing Alumina Whiskers: Influence of Filler Functionalization on Dielectric Properties

    Directory of Open Access Journals (Sweden)

    Pietro Russo

    2014-01-01

    Full Text Available Poly(butylene terephthalate (PBT is one of the most widely used semicrystalline thermoplastics polyester because of its superior thermal and mechanical properties, high dimensional stability and excellent processability. In this research PBT-based nanocomposites, including various amounts (up to 10 wt% of commercial alumina whiskers, have been prepared by using a Brabender internal chamber mixer and analysed in terms of morphological features and dielectric properties. Specific attention has been focused on the effect of the filler functionalization considering 3-glycidoxy propylmethoxysilane (GPS or 3-methacryloxypropyltrimethoxysilane (MPS as coupling agents. Tests, performed on compounds filled with neat and functionalized alumina whiskers, show a clear dependence of relative dielectric permittivity εr, invariance of dissipation factor (tgδ, and a sensible increase of volume electrical resistivity (ρv with the filler’s content and are encouraging for a future introduction of such composites in many electrical applications.

  9. MELT BLENDS OF POLY(BUTYLENE TEREPHTHALATE) AND A THERMOTROPIC LIQUID CRYSTALLINE POLYMER

    Institute of Scientific and Technical Information of China (English)

    HE Jiasong; BU Wensheng; ZHANG Hongzhi; ZHENG Suyun; XU Xiangqin

    1994-01-01

    With the help of differential scanning calorimetry, cone-plate and capillary rheometry and scanning electron microscopy, a research has been conducted on rheological behavior,crystallization and morphology of poly (butylene terephthalate) (PBT) blends containing a thermotropic LCP. The blend has zero entrance pressure loss, although the LCP has rather large one. The viscosity curve of the blend lies between those of the LCP and PBT. The crystallization of PBT is not affected by the presence of the LCP together with no indication of transesterification between the two ingredients. LCP spheres and ellipsoids with the size of 0.5-1. 5 μm disperse in PBT matrix uniformly, which is related to the viscosity ratio of the two components.

  10. Electron beam-induced crosslinking of poly(butylene adipate-co-terephthalate)

    International Nuclear Information System (INIS)

    Biodegradable poly(butylene adipate-co-terephthalate) (PBAT) was crosslinked by electron beam irradiation and their properties were investigated in this research. PBAT films prepared by a solution casting method were crosslinked by electron beam under various absorbed doses ranging 20-200 kGy and their properties were characterized by using a crosslinking degree measurement, a thermogravimetric analyzer (TGA), universal testing machine (UTM), dynamic mechanical analyzer (DMA), and thermal mechanical analyzer (TMA). The results of the crosslinking degree measurement revealed that the PBAT could be crosslinked by electron beam irradiation and its crosslinking degree was dependant on the absorbed dose. In addition, the results of the UTM, DMA, TMA, and TGA analyses revealed that the thermal and mechanical properties of the crosslinked PBS was much improved in comparison to those of the control PBAT.

  11. Characterization of clay filled poly (butylene terephthalate nanocomposites prepared by solution blending

    Directory of Open Access Journals (Sweden)

    Khalid Saeed

    2015-01-01

    Full Text Available Abstract Kaolin clay/poly (butylene terephthalate (clay/PBT composites films were prepared by solution casting technique. The scanning electron microscope (SEM study showed that clay particles were well dispersed and embedded within the PBT matrix. The TGA thermograms showed that the thermal stability of PBT matrix was slightly improved by the incorporation of clay into the polymer matrix. The polarized optical microscopy (POM study presented that the size of spherulites of PBT was decreased by the incorporation of clay into matrix, which might be due to nucleation effect of kaolin clay. The tensile strength and modulii of PBT polymer matrix were also significantly improved by the addition of clay polymer matrix. The solvent uptake study showed that the uptake of various solvents by clay/PBT nanocomposite were lower than neat PBT.

  12. Biocompatibility and characterization of polylactic acid/styrene-ethylene-butylene-styrene composites.

    Science.gov (United States)

    Tsou, Chi-Hui; Kao, Bo-Jyue; Yang, Ming-Chien; Suen, Maw-Cherng; Lee, Yi-Hsuan; Chen, Jui-Chin; Yao, Wei-Hua; Lin, Shang-Ming; Tsou, Chih-Yuan; Huang, Shu-Hsien; De Guzman, Manuel; Hung, Wei-Song

    2015-01-01

    Polylactic acid (PLA)/styrene-ethylene-butylene-styrene (SEBS) composites were prepared by melt blending. Differential scanning calorimetry (DSC) and wide angle X-ray diffraction (WXRD) were used to characterize PLA and PLA/SEBS composites in terms of their melting behavior and crystallization. Curves from thermal gravimetric analysis (TGA) illustrated that thermostability increased with SEBS content. Further morphological analysis of PLA/SEBS composites revealed that SEBS molecules were not miscible with PLA molecules in PLA/SEBS composites. The tensile testing for PLA and PLA/SEBS composites showed that the elongation at the break was enhanced, but tensile strength decreased with increasing SEBS content. L929 fibroblast cells were chosen to assess the cytocompatibility; the cell growth of PLA was found to decrease with increasing SEBS content. This study proposes possible reasons for these properties of PLA/SEBS composites.

  13. Poly(lactide)-g-poly(butylene succinate-co-adipate) with High Crystallization Capacity and Migration Resistance

    OpenAIRE

    Xi Yang; Huan Xu; Karin Odelius; Minna Hakkarainen

    2016-01-01

    Plasticized polylactide (PLA) with increased crystallization ability and prolonged life-span in practical applications due to the minimal plasticizer migration was prepared. Branched plasticized PLA was successfully obtained by coupling poly(butylene succinate-co-adipate) (PBSA) to crotonic acid (CA) functionalized PLA. The plasticization behavior of PBSA coupled PLA (PLA-CA-PBSA) and its counterpart PBSA blended PLA (PLA/PBSA) were fully elucidated. For both PLA-CA-PBSA and PLA/PBSA, a decre...

  14. DIGITAL IMAGE ANALYSIS OF PHASE STRUCTURE IN THE BLEND OF POLY(BUTYLENE TEREPHTHALATE-COCAPROLACTONE) WITH POLYCARBONATE

    Institute of Scientific and Technical Information of China (English)

    MA Dezhu; HE Liling; ZOU Yingfang; LUO Xiaolie; Takafumi Hayashi; Toshio Nishi

    1992-01-01

    The digital image processing technique was used for the extraction of physical information from the temporal image of phase structure in the process of phase separation in the blend of poly (butylene terephthalate-co-caprolactone )with polycarbonate. The power spectrum images of the two-dimensional Fourier transformation (2DFT) of the temporal image of phase structure reflect the change of the phase size with time.

  15. Ethylene oxide-block-butylene oxide copolymer uptake by silicone hydrogel contact lens materials

    Energy Technology Data Exchange (ETDEWEB)

    Huo, Yuchen [Department of Materials Science and Engineering, University of Florida, Rhines Hall 100, Gainesville, FL 32611 (United States); Ketelson, Howard [Alcon Inc., Research and Development, Vision Care, 6201 South Freeway, Fort Worth, TX 76134 (United States); Perry, Scott S., E-mail: ssp@mse.ufl.edu [Department of Materials Science and Engineering, University of Florida, Rhines Hall 100, Gainesville, FL 32611 (United States)

    2013-05-15

    Four major types of silicone hydrogel contact lens material have been investigated following treatments in aqueous solutions containing poly(ethylene oxide) and poly(butylenes oxide) block copolymer (EO–BO). The extent of lens surface modification by EO–BO and the degree of bulk uptake were studied using X-ray photoelectron spectroscopy (XPS) and ultra-performance liquid chromatography (UPLC), respectively. The experimental results suggest that different interaction models exist for the lenses, highlighting the influence of both surface and bulk composition, which greatly differs between the lenses examined. Specifically, lenses with hydrophilic surface treatments, i.e., PureVision{sup ®} (balafilcon A) and O{sub 2}OPTIX (lotrafilcon B), demonstrated strong evidence of preferential surface adsorption within the near-surface region. In comparison, surface adsorption on ACUVUE{sup ®} Oasys{sup ®} (senofilcon A) and Biofinity{sup ®} (comfilcon A) was limited. As for bulk absorption, the amount of EO–BO uptake was the greatest for balafilcon A and comfilcon A, and least for lotrafilcon B. These findings confirm the presence of molecular concentration gradients within the silicone hydrogel lenses following exposure to EO–BO solutions, with the nature of such concentration gradients found to be lens-specific. Together, the results suggest opportunities for compositional modifications of lenses for improved performance via solution treatments containing surface-active agents.

  16. The degradation and adsorption behaviors of enzyme on poly(butylene succinate) single crystals.

    Science.gov (United States)

    Jiang, Xi; Yang, Ju-Ping; Wang, Xiao-Hong; Zhou, Jian-Jun; Li, Lin

    2009-12-01

    The enzymatic degradation behavior of poly(butylene succinate) (PBS) single crystals with a lipase from Pseudomonas cepacia (lipase PS) is monitored using atomic force microscopy (AFM) in phosphate buffer at pH 6.8 and 40 degrees C. In-situ AFM results show that enzymatic degradation of the single crystal starts from the crystal edges rather than the chain-folded surfaces and the lamellar thickness remains constant during the whole degradation process. Total internal reflection fluorescence microscopy (TIRFM) is used for the first time to study the adsorption behavior of lipase onto the PBS crystal surface. The results clearly show that the enzyme molecules preferentially adsorb on the lateral surfaces of the single crystal but not on the chain-folded surfaces. AFM force-distance curve measurements and force-volume imaging obtained using a lipase-immobilized AFM tip show that small and large adhesive forces exist in the flat-on and edge-on areas of a PBS banded spherulite, respectively, which correspond to the chain-folded surface and lateral edges of a single crystal. PMID:19953521

  17. Solubilization of docetaxel in poly(ethylene oxide)-block-poly(butylene/styrene oxide) micelles.

    Science.gov (United States)

    Elsabahy, Mahmoud; Perron, Marie-Eve; Bertrand, Nicolas; Yu, Ga-Er; Leroux, Jean-Christophe

    2007-07-01

    Poly(ethylene oxide)-block-poly(styrene oxide) (PEO-b-PSO) and PEO-b-poly(butylene oxide) (PEO-b-PBO) of different chain lengths were synthesized and characterized for their self-assembling properties in water by dynamic/static light scattering, spectrofluorimetry, and transmission electron microscopy. The resulting polymeric micelles were evaluated for their ability to solubilize and protect the anticancer drug docetaxel (DCTX) from degradation. The drug release kinetics as well as the cytotoxicity of the loaded micelles were assessed in vitro. All polymers formed micelles with a highly viscous core at low critical association concentrations (<10 mg/L). Micelle morphology depended on the nature of the hydrophobic block, with PBO- and PSO-based micelles yielding monodisperse spherical and cylindrical nanosized aggregates, respectively. The maximum solubilization capacity for DCTX ranged from 0.7 to 4.2% and was the highest for PSO micelles exhibiting the longest hydrophobic segment. Despite their high affinity for DCTX, PEO-b-PSO micelles were not able to efficiently protect DCTX against hydrolysis under accelerated stability testing conditions. Only PEO-b-PBO bearing 24 BO units afforded significant protection against degradation. In vitro, DCTX was released slower from the latter micelles, but all formulations possessed a similar cytotoxic effect against PC-3 prostate cancer cells. These data suggest that PEO-b-P(SO/BO) micelles could be used as alternatives to conventional surfactants for the solubilization of taxanes. PMID:17579476

  18. Preparation and characterization of nanocomposite of maleated poly(butylene adipate-co-terephthalate) with organoclay.

    Science.gov (United States)

    Chen, Jung-Hung; Yang, Ming-Chien

    2015-01-01

    Nanocomposites of poly(butylene adipate-co-terephthalate) (PBAT) with montmorillonite (MMT) nanoparticles were prepared via melt blending. Natural MMT was modified by either octadecylamine (ODA) or dihexylamine (DHA). Neat PBAT was grafted with maleic anhydride via melt grafting process. Intercalation of the organoclay in the PBAT matrix was studied by X-ray diffraction (XRD). From the results of transmission electron microscope (TEM), the dispersion of ODA-modified MMT in the PBAT matrix was more homogeneous than that of neat MMT. The addition of organoclay can increase the cooling crystallization temperature of PBAT, as observed by differential scanning calorimetry (DSC). Furthermore, the results of thermogravimetric analyzer (TGA) showed that the addition of ODA-modified MMT can improve the thermal stability of PBAT nanocomposites. The tensile strength was little affected, while the Young's modulus was increased with the addition of nanoclays. The grafting of PBAT with MA resulted in improved interaction between polymer matrix and the silicate layer due to the formation of chemical/physical bonds, thus the dispersion of organoclays was enhanced. By grafting PBAT with MA, the enzymatic biodegradation of the nanocomposite was increased, while the photodegradation of PBAT was little affected. Furthermore, the transmission of water vapor was reduced by the addition of organically modified MMT. PMID:25491991

  19. Dispersion study of nanofibrillated cellulose based poly(butylene adipate-co-terephthalate) composites.

    Science.gov (United States)

    Mukherjee, Tapasi; Czaka, Michael; Kao, Nhol; Gupta, Rahul K; Choi, Hyoung Jin; Bhattacharya, Sati

    2014-02-15

    The production of lower cost bionanocomposites based on nanofibrillated cellulose (NFC) is a promising source to develop the next generation of light weight and high performance materials for a variety of defense, infrastructure and energy applications. In this study, a series of bio-nanocomposites were developed by reinforcing NFC from regenerated wood fiber into poly(butylene adipate-co-terephthalate) (PBAT) by injection molding. The incorporation of NFC in PBAT matrix (0.2-1 wt%) increased the storage modulus (G') and dynamic viscosity (η') as revealed by shear rheology, indicating a percolation threshold around 0.2-0.5 wt% region. DSC analysis showed similar trends with slight improvement of glass transition (Tg) and crystallization temperature (Tc). Percentage crystallinity, as calculated from heat of fusion equation and taking into account 100% crystallized PBAT data improved in overall. This is a fundamental study aimed at understanding the morphological, rheological and thermal evaluation of such nanocomposites for an improved dispersion of NFC as filler in the matrix. PMID:24507316

  20. Thermal and Mechanical Properties of Poly(butylene succinate Films Reinforced with Silica

    Directory of Open Access Journals (Sweden)

    Sangviroon Nanthaporn

    2015-01-01

    Full Text Available In recent year, bioplastics have become more popular resulting from the growing concerns on environmental issues and the rising fossil fuel price. However, their applications were limited by its mechanical and thermal properties. The aim of this research is thus to improve mechanical and thermal properties of PBS bioplastic films by reinforcing with silica. Due to the poor interfacial interaction between the PBS matrix and silica, glycidyl methacrylate grafted poly(butylene succinate (PBS-g-GMA was used as a compatibilizer in order to improve the interaction between bioplastic films and filler. PBS-g-GMA was prepared in a twin-screw extruder and analyzed by the FTIR spectrometer. PBS and silica were then mixed in a twin-screw extruder and processed into films by a chill-roll cast extruder. The effects of silica loading on thermal and mechanical properties of the prepared bioplastic films were investigated. It was found that the mechanical properties of PBS/silica composite films were improved when 1%wt of silica was added. However, the mechanical properties decreased with increasing silica loading due to the agglomeration of silica particles. The results also show that the silica/PBS films with PBS-g-GMA possessed improved mechanical properties over the films without the compatibilizer.

  1. Dispersion of multi-walled carbon nanotubes in biodegradable poly(butylene succinate) matrix.

    Science.gov (United States)

    Ray, Suprakas Sinha; Vaudreuil, Sébastien; Maazouz, Abderrahim; Bousmina, Mosto

    2006-07-01

    This communication describes the preparation, characterization and properties of biodegradable poly(butylene succinate) (PBS)/multi-walled carbon nanotubes (MWCNTs) nanocomposite. Nanocomposite was prepared by melt-blending in a batch mixer and the amount of MWCNTs loading was 3 wt%. State of dispersion-distribution of the MWCNTs in the PBS matrix was examined by scanning and transmission electron microscopic observations that revealed homogeneous distribution of stacked MWCNTs in PBS matrix. The investigation of the thermomechanical behavior was performed by dynamic mechanical thermal analysis. Results demonstrated substantial enhancement in the mechanical properties of PBS, for example, at room temperature, storage flexural modulus increased from 0.64 GPa for pure PBS to 1.2 GPa for the nanocomposite, an increase of about 88% in the value of the elastic modulus. The tensile modulus and thermal stability of PBS were moderately improved after nanocomposite preparation with 3 wt% of MWCNTs, while electrical conductivity of neat PBS dramatically increased after nanocomposite formation. For example, the in plane conductivity increased from 5.8 x 10(-9) S/cm for neat PBS to 4.4 x 10(-3) for nanocomposite, an increase of 10(6) fold in value of the electrical conductivity. PMID:17025148

  2. Effect of gamma irradiation on poly(butylene naphthalate) based polyesters

    Science.gov (United States)

    Malavasi, I.; Consolati, G.; Quasso, F.; Soccio, M.; Gigli, M.; Negrin, M.; Macerata, E.; Giacobbo, F.; Lotti, N.; Munari, A.; Mariani, M.

    2016-07-01

    The present work investigates the effect of gamma radiation on the properties of three naphthalate-based polyesters, i.e. poly(butylene naphthalate) (PBN), poly(diethylene naphthalate) (PDEN) and poly(thiodiethylene naphthalate) (PTDEN). In addition, the analogous terephthalate-based polymers of PDEN and PTDEN, i.e. poly(diethylene terephthalate) (PDET) and poly(thiodiethylene terephthalate) (PTDET), are also investigated, in order to check the effect of a lower number of aromatic rings. All the polymers, irradiated in air at different absorbed doses, were characterized by several techniques. The data obtained indicate that all the polymers, except PBN, show a decrease of molecular weight with the dose increase. The thermal behavior and the morphology confirm the previous results and show that the higher the crystallinity degree and number of aromatic rings, the higher the radiation resistance. The introduction of heteroatoms decreases the ability of a polymer to crystallize due to a reduction of polymer chain symmetry, thus worsening their radiation resistance.

  3. NONISOTHERMAL CRYSTALLIZATION AND MORPHOLOGY OF POLY(BUTYLENE SUCCINATE)/LAYERED DOUBLE HYDROXIDE NANOCOMPOSITES

    Institute of Scientific and Technical Information of China (English)

    Mei-qiu Zhan; Guang-yi Chen; Zhi-yong Wei; Yu-mei Shi; Wan-xi Zhang

    2013-01-01

    Biodegradable poly(butylene succinate) (PBS) and layered double hydroxide (LDH) nanocomposites were prepared via melt blending in a twin-screw extruder.The morphology and dispersion of LDH nanoparticles within PBS matrix were characterized by transmission electron microscopy (TEM),which showed that LDH nanoparticles were found to be well distributed at the nanometer level.The nonisothermal crystallization behavior of nanocomposites was extensively studied using differential scanning calorimetry (DSC) technique at various cooling rates.The crystallization rate of PBS was accelerated by the addition of LDH due to its heterogeneous nucleation effect; however,the crystallization mechanism and crystal structure of PBS remained almost unchanged.In kinetics analysis of nonisothermal crystallization,the Ozawa approach failed to describe the crystallization behavior of PBS/LDH nanocomposites,whereas both the modified Avrami model and the Mo method well represented the crystallization behavior of nanocomposites.The effective activation energy was estimated as a function of the relative degree of crystallinity using the isoconversional analysis.The subsequent melting behavior of PBS and PBS/LDH nanocomposites was observed to be dependent on the cooling rate.The POM showed that the small and less perfect crystals were formed in nanocomposites.

  4. Analysis of Gas Permeability Characteristics of Poly(Lactic Acid/Poly(Butylene Succinate Nanocomposites

    Directory of Open Access Journals (Sweden)

    Amita Bhatia

    2012-01-01

    Full Text Available Gas permeability and morphological properties of nanocomposites prepared by the mixing of poly(lactic acid (PLA, poly(butylene succinate (PBS, and clay was investigated. While the composition of PLA and PBS polymers was fixed as 80% and 20% by weight, respectively, for all the nanocomposites, clay contents varied from 1 to 10 wt%. From the morphological studies using both wide angle X-ray diffraction and transmission electron microscopy, the nanocomposite having 1 wt% of clay was considered to have a mixed morphology of intercalated and delaminated structure, while some clusters or agglomerated particles were detected for nanocomposites having 3 and more than 3 wt% of clay content. However, the average particle size of the dispersed PBS phase was reduced significantly from 7 μm to 30–40 nm with the addition of clay in the blend. The oxygen barrier property was improved significantly as compared to the water vapor. A model based on gas barrier property was used for the validation of the oxygen relative permeabilities of PLA/PBS/clay nanocomposites. PLA/PBS/clay nanocomposites validated the Bharadwaj model up to 3 wt% of clay contents only, while for nanocomposites of higher clay contents the Bharadwaj model was invalid due to the clusters and agglomerates formed.

  5. Poly(butylene cyclohexanedicarboxylate/diglycolate random copolymers reinforced with SWCNTs for multifunctional conductive biopolymer composites

    Directory of Open Access Journals (Sweden)

    E. Fortunati

    2016-02-01

    Full Text Available The objective of this work was to develop a versatile strategy for preparing multifunctional composite films with tunable properties. Novel conductive composites based on the combination of single walled carbon nanotubes (SWCNTs and biodegradable poly(butylene cyclohexanedicarboxylate/diglycolate random copolymers (P(BCEmBDGn are here presented. In particular, synthesized PBCE homopolymer and two copolymers containing different amounts of ether–oxygen containing co-units, P(BCE90BDG10 and P(BCE70BDG30, have been considered as matrices of SWCNTs based composites. The effect of incorporation of different amounts of SWCNTs (0.1–0.5–0.75–1 wt% on morphological, thermal, mechanical and electrical properties was deeply investigated. The morphology of the fracture surfaces is affected by the SWCNT presence, while the increase in the SWCNT content does not provide significant microstructure modifications. The thermal properties underlined that nanotubes can act as nucleating agents, favouring the polymer crystallization process. The mechanical behavior demonstrated that the introduction of carbon nanotubes both in the case of PBCE homopolymer and in random copolymers based formulations exerted a reinforcing effect. All composites exhibit high electrical conductivity in comparison to the neat polymers. This work demonstrates that this combinatorial approach can be used to develop materials with tunable and advanced functional properties.

  6. Effects of Radiation on Mechanical Properties of Poly (butylene succinate) and Cassava Starch Blends

    International Nuclear Information System (INIS)

    This research compared the effects of gamma and electron beam irradiation at different doses on the mechanical properties of polymer blends between poly(butylene succinate) (PBS) and cassava starch. Two types of starch were used to prepare thermoplastic starch (TPS), native cassava starch and hydrophobic starch. PBS/TPS blends were compounded at five different weight ratios using a twin-screw extruder. Mechanical properties and degradation were evaluated in comparison to unirradiated samples. Results indicated that the incorpora- tion of TPS prepared from native cassava starch decreased the mechanical properties of PBS/TPS blends, whereas the addition of TPS prepared from hydrophobic starch improved the mechanical properties of the blends. In addition, the maximum mechanical properties of PBS/TPS blends were achieved when samples were exposed to irradiation at 120 kGy. Using soil burial evaluation, the degradation rate of blends was found to increase with the addition of TPS. Therefore we have demonstrated in this study that the type of TPS and irradiation treatment can significantly alter the mechanical properties and degradation of PBS/TPS blends.

  7. Surface analysis of BPA-polycarbonate/ poly(butylene terephthalate) blends by X-ray photoelectron spectroscopy

    Science.gov (United States)

    Burrell, Michael C.; Chera, John J.

    1988-10-01

    X-ray photoelectron spectroscopy is used to measure the surface composition of polycarbonate/ poly(butylene terephthalate) blends. The blend surface is enriched in PC compared to the bulk, with the surface PC/PBT ratio equal to about 1.6 times to bulk formation. For blends containing an impact modifier as a third component, the XPS spectra of the molded surface indicates that no impact modifier is present within the XPS sampling depth. A spectral simulation scheme improves the accuracy of the computed PC/PBT ratio over conventional data reduction schemes involving curve fitting.

  8. The Electroluminescence Characterization of Poly(p-phenyleneethynylene)——The π-conjugated Backbone Interrupted by a Butylene Unit

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    π-Conjugated poly(p-phenyleneethynylene) with the interruption of the conjugation by a butylene unit was synthesized. Its absorption, PL and EL spectra were investigated respectively. The spectral peaks shifted to the higher energy side with the interruption of the conjugation lengths. The model compound was synthesized, by which the results were proved. The thermal characteristics of the polymer was determined by DSC and TGA, indicating that the polymer has a good thermal stability. The electroluminescence(EL) in the green region of the spectrum with a maximum at 500 nm was observed from the polymer films sandwiched between indium-tin-oxide and an Al electrode.

  9. Effect of Anodic Alumina Oxide Pore Diameter on the Crystallization of Poly(butylene adipate).

    Science.gov (United States)

    Sun, Xiaoli; Fang, Qunqun; Li, Huihui; Ren, Zhongjie; Yan, Shouke

    2016-04-01

    Poly(butylene adipate) (PBA) was infiltrated into the anodic alumina oxide (AAO) templates with the pore diameter of around 30, 70, and 100 nm and PBA nanotubes with different diameters were prepared. The crystallization and phase transition behavior of the obtained PBA nanotubes capped in the nanopores have been explored by using X-ray diffraction and differential scanning calorimetry. Only α-PBA crystals form in the bulk sample during nonisothermal crystallization. By contrast, predominant β-PBA crystals form in the AAO templates. The β-PBA crystals formed in the nanopores with pore diameter less than 70 nm prefer to adopt an orientation with their b-axis parallel to the long axis of the pore. During the melt recrystallization, it was found that the critical temperature (Tβ), below which pure β-crystals form, is 20 °C for bulk PBA. It drops down significantly with the pore diameter for the PBA in the AAO template. Moreover, the β-crystals in the porous template exhibit larger lattice parameters compared with the bulk crystals. By monitoring the change of β-crystals in the heating process, it was found that β-crystals in the AAO template with the pore diameter of 30 nm (D30) melt directly while the β-crystals transform to α-crystals in the template with the pore diameter of 100 nm (D100). The intensity of (020) Bragg peak of β-crystals decreases at a similar rate in both D30 and D100 but disappears at a relatively lower temperature in D30. On the other hand, the β(110) peak intensity of β-PBA crystals formed in the D100 template decreases first at slower rate before α crystals appear, and then at a faster rate once the β to α phase transition takes place. PMID:27008378

  10. Preparation and characterization of nanocomposite of maleated poly(butylene adipate-co-terephthalate) with organoclay

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Jung-Hung [Graduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, Taipei 10607, Taiwan (China); Yang, Ming-Chien, E-mail: myang@mail.ntust.edu.tw [Graduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, Taipei 10607, Taiwan (China); Department of Materials Science and Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan (China)

    2015-01-01

    Nanocomposites of poly(butylene adipate-co-terephthalate) (PBAT) with montmorillonite (MMT) nanoparticles were prepared via melt blending. Natural MMT was modified by either octadecylamine (ODA) or dihexylamine (DHA). Neat PBAT was grafted with maleic anhydride via melt grafting process. Intercalation of the organoclay in the PBAT matrix was studied by X-ray diffraction (XRD). From the results of transmission electron microscope (TEM), the dispersion of ODA-modified MMT in the PBAT matrix was more homogeneous than that of neat MMT. The addition of organoclay can increase the cooling crystallization temperature of PBAT, as observed by differential scanning calorimetry (DSC). Furthermore, the results of thermogravimetric analyzer (TGA) showed that the addition of ODA-modified MMT can improve the thermal stability of PBAT nanocomposites. The tensile strength was little affected, while the Young's modulus was increased with the addition of nanoclays. The grafting of PBAT with MA resulted in improved interaction between polymer matrix and the silicate layer due to the formation of chemical/physical bonds, thus the dispersion of organoclays was enhanced. By grafting PBAT with MA, the enzymatic biodegradation of the nanocomposite was increased, while the photodegradation of PBAT was little affected. Furthermore, the transmission of water vapor was reduced by the addition of organically modified MMT. - Highlights: • Nanocomposites of PBAT and clay nanoparticles were prepared via melting blending. • Maleated PBAT/organoclays exhibited higher Young's moduli than neat PBAT/neat MMT. • The enzymatic degradation of PBAT composites was improved by maleation. • Maleation caused little effect on the photodegradation of PBAT. • Organoclays retarded the permeation of water vapor through PBAT composites.

  11. Biodegradation of poly(lactic acid, poly(hydroxybutyrate-co-hydroxyvalerate, poly(butylene succinate and poly(butylene adipate-co-terephthalate under anaerobic and oxygen limited thermophilic conditions

    Directory of Open Access Journals (Sweden)

    Jutakan Boonmee

    2016-01-01

    Full Text Available In order to study the biodegradation behavior of biodegradable plastics in landfill conditions, four types of biodegradable plastics including poly(lactic acid (PLA, poly(hydroxybutyrate-co-hydroxyvalerate (PHBV, poly(butylene succinate (PBS, and poly(butylene adipate-co-terephthalate (PBAT were tested by burying in sludge mixed soil medium under anaerobic and oxygen limited conditions. The experiments were operated at 52 ± 2ºC in dark conditions according to ISO15985. The degree of biodegradation after 75 days was investigated by weight loss determination, visual examination, and surface appearance by scanning electronic microscopy (SEM. Under both anaerobic and oxygen limited conditions, the complete degradation (100% weight loss was found only in PHBV after 75 days. The plastic degradations were ranked in the order of PHBV> PLA> PBS> PBAT. The percentage of weight losses were significantly different at p ≤ 0.05. However, for all studied plastics, the degradation under anaerobic and oxygen limited conditions did not significantly different at 95% confidence.

  12. TRANSESTERIFICATION OF POLY(BISPHENOL A CARBONATE) WITH AROMATIC AND ALIPHATIC SEGMENTS IN BUTYLENE TEREPHTHALATE-CAPROLACTONE COPOLYESTER

    Institute of Scientific and Technical Information of China (English)

    Song Wang; Yi-ping Huang; Xiao-lie Luo; De-zhu Ma

    2004-01-01

    In this article, the transesterification ofpoly(bisphenol A carbonate) (PC) with butylene terephthalate-caprolactone copolyester at a weight ratio 50/50 (BCL(21)) was thoroughly investigated by proton nuclear magnetic resonance spectroscopy (1H-NMR), in conjunction with a model compound. The 1H-NMR results of the annealed blend PC/BCL(21)show that the formation of bisphenol A-terephthalate ester units is the same as in the annealed blend of PC with PBT, and the transesterification actually occurs between PC and butylene terephthalate (BT) segments in BCL(21). By comparison with the model compound bisphenol A dibutyrate, the new signal appearing at δ = 2.56 in the 1H-NMR spectrum confirms the existence of bisphenol A caprolactone ester units resulting from the exchange reaction of PC with caprolactone (CL)segments. 1H-NMR analysis of the transesterification rates reveals that the reaction of PC with aromatic and aliphatic segments in BCL(21) proceeds in a random manner. The miscibility of the blend PC/BCL(21) copolyester is favorable for the transesterification of PC with BT segments and CL segments.

  13. Effect of peroxide and chain extender on mechanical properties and morphology of poly (butylene succinate)/poly (lactic acid) blends

    Science.gov (United States)

    Cherykhunthod, W.; Seadan, M.; Suttiruengwong, S.

    2015-07-01

    Poly (butylene succinate) (PBS) and poly (lactic acid) (PLA) are biodegradable polymers with high potential to replace commodity fossil-based polymers in a wide range of applications. However, these two polymers are immiscible in most ratios, but partially miscible when one of the two is a major phase. In this study, a one-step process in a twin-screw extruder was used to prepare the blends between poly (butylene succinate) (PBS) as a matrix and poly (lactic acid) (PLA) as a dispersed phase. To improve mechanical properties and morphology of blends, two reactive agents, peroxide (Perkadox) and multifunctional epoxide chain extender (Joncryl) were selected and compared. All samples were characterized for melt flow index (MFI), morphology, tensile, and impact properties. The results showed that the mechanical properties and morphology of PBS/PLA blends were improved when using both reactive agents. It was demonstrated that the increased mechanical properties resulted from good interfacial adhesion between PBS and finely dispersed PLA particles. The addition of 0.075 phr Perkadox to PBS/PLA (75:25 and 80:20) blends increased elongation at break by 7.2% and 38.4%, respectively compared with the blends without reactive agents. The results from gel content also revealed the graft copolymer existed at the interface when reactive agents were added. In the case of using multifunctional epoxide chain extender, the impact strength of the blends increased.

  14. Controlled-release fertilizer prepared using a biodegradable aliphatic copolyester of poly(butylene succinate) and dimerized fatty acid.

    Science.gov (United States)

    Lubkowski, Krzysztof; Smorowska, Aleksandra; Grzmil, Barbara; Kozłowska, Agnieszka

    2015-03-18

    The preparation and characterization of a controlled-release multicomponent (NPK) fertilizer with the coating layer consisting of a biodegradable copolymer of poly(butylene succinate) and a butylene ester of dilinoleic acid (PBS/DLA) is reported. The morphology and structure of the resulting polymer-coated materials and the thickness of the covering layers were examined using X-ray diffraction and scanning electron microscopy coupled with energy dispersive X-ray analysis. The mechanical properties of these materials were determined with a strength-testing machine. Nutrient release was measured in water using spectrophotometry, potentiometry, and conductivity methods. The results of the nutrient release experiments from these polymer-coated materials were compared with the requirements for controlled-release fertilizers. A conceptual model is presented describing the mechanism of nutrient release from the materials prepared in this study. This model is based on the concentrations of mineral components inside the water-penetrated fertilizer granules, the diffusion properties of the nutrients in water, and a diffusion coefficient through the polymer layer. The experimental kinetic data on nutrient release were interpreted using the sigmoidal model equation developed in this study. PMID:25715823

  15. Effect of planar extension on the structure and mechanical properties of polystyrene-poly(ethylene-¤co¤-butylene)-polystyrene triblock copolymers

    DEFF Research Database (Denmark)

    Daniel, C.; Hamley, I.W.; Mortensen, K.

    2000-01-01

    Two thermoplastic poly(styrene)-poly(ethylene-co-butylene) -poly(styrene) triblock copolymers containing either spherical or cylindrical poly(styrene) microdomains were pre-oriented through extensional flow. Small angle neutron scattering (SANS) measurements revealed that the pre-oriented triblock...

  16. Alternating polyesteramides based on 1,4-butylene terephthalamide: 3. Alternating polyesteramides based on mixtures of linear diols (4NTm,p)

    NARCIS (Netherlands)

    Serrano, P.J.M.; Werff, van der B.A.; Gaymans, R.J.

    1998-01-01

    Strictly alternating polyesteramides consisting of 1,4-butylene terephthalamide diester and mixtures of aliphatic diols have been synthesised in the melt in the presence of a titanium catalyst. To increase the molecular weight a solid state post condensation was applied. The composition was determin

  17. Morphology, melting behavior, and non-isothermal crystallization of poly(butylene terephthalate)/poly(ethylene-co-methacrylic acid) blends

    Energy Technology Data Exchange (ETDEWEB)

    Huang, J.-W. [Department of Styling and Cosmetology, Tainan University of Technology, 529 Chung Cheng Rd., Yung Kang City 710, Taiwan (China)], E-mail: jw.huang@msa.hinet.net; Wen, Y.-L. [Department of Nursing, Meiho Institute of Technology, 23 Ping Kuang Rd., Neipu Hsiang, Pingtung 912, Taiwan (China); Department of Resources Engineering, National Cheng Kung University, No. 1, University Rd., Tainan City 701, Taiwan (China); Kang, C.-C. [R and D Center, Hi-End Polymer Film Co., Ltd. 15-1 Sin Jhong Rd., Sin Ying City 730, Taiwan (China); Yeh, M.-Y. [Department of Chemistry, National Cheng Kung University, No. 1, University Rd., Tainan City 701, Taiwan (China); Sustainable Environment Research Centre, National Cheng Kung University, Taiwan (China); Wen, S.-B. [Department of Nursing, Meiho Institute of Technology, 23 Ping Kuang Rd., Neipu Hsiang, Pingtung 912, Taiwan (China); Department of Resources Engineering, National Cheng Kung University, No. 1, University Rd., Tainan City 701, Taiwan (China)

    2007-12-15

    The morphology, melting behavior, and non-isothermal crystallization of poly(butylene terephthalate) (PBT) and poly(ethylene-co-methacrylic acid) (PEMA) blends were studied with scanning electron microscopy, X-ray diffraction and differential scanning calorimetry (DSC). PEMA forms immiscible, yet compatible, blends with PBT. Subsequent DSC scans on melt-crystallized samples exhibited two melting endotherms (T{sub mI} and T{sub mII}). The presence of PEMA would facilitate the recrystallization during heating scan and retard PBT molecular chains to form a perfect crystal in cooling crystallization. The dispersion phases of molten PEMA acts as nucleating agents to enhance the crystallization rate of PBT. The solidified PBT could act as nucleating agents to enhance the crystallization of PEMA, but also retard the molecular mobility to reduce crystallization rate. The U* and K{sub g} of Hoffman-Lauritzen theory were also determined by Vyazovkin's methods to support the interpretation.

  18. Effect of Anorganic Substance on Physical Properties of Poly (Butylene Succinate -co- Adipate) Irradiated by Electron Beam

    International Nuclear Information System (INIS)

    Poly(butylene succinate-co-adipate), PBSA were electron beam irradiated in the presence of inorganic materials. The samples gave high gel fraction by irradiation in the presence of 2% silicon dioxide and 2% carbon black. It was found that addition of carbon black (CB) was effective for improving the heat stability of the sample. This is because of three-dimensional carbon black- polymer networks. Irradiated PBSA sheets broke immediately at 110 oC with load 6.67 kgf/cm2, while irradiated the same sample mixed with 2% carbon black did not break at the same condition. Biodegradability of crosslinked PBSA by soil burial tests was accelerated by addition of carbon black. (author)

  19. Stabilization of polypropylene, polypropylene blends with poly (styrene-b-(ethylene-co-butylene)-b-styrene) under irradiation: A comparative investigation

    Energy Technology Data Exchange (ETDEWEB)

    Luan Shifang; Yang Huawei; Shi Hengchong; Zhao Jie [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Wang Jianwei [Shandong Weigao Group Medical Polymer Company Limited, Weihai 264209 (China); Yin Jinghua, E-mail: yinjh@ciac.jl.c [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China)

    2011-01-15

    The aim of this paper is to investigate the stabilization of polypropylene in the poly (styrene-b-(ethylene-co-butylene)-b-styrene) (SEBS)/polypropylene (PP) blends under irradiation with respect to PP. The PP films, SEBS/PP films were subjected to electron beam irradiation and characterized by wide angle X-ray diffraction (WAXD), differential scanning calorimetry (DSC), gel permeation chromatography (GPC), and dynamic mechanical thermal analysis (DMTA). It demonstrated that upon irradiation, the molecular weight of PP had a pronounced decrease due to the major chain scission, and the minor chain cross-linking or chain branching occurred at the higher irradiation dose. Stabilization of PP was improved in the presence of SEBS, exhibiting an enhanced irradiation resistance.

  20. Non-isothermal crystallization kinetics and characterization of biodegradable poly(butylene succinate-co-neopentyl glycol succinate) copolyesters.

    Science.gov (United States)

    Xie, Wen-Jie; Zhou, Xiao-Ming

    2015-01-01

    Both biodegradable aliphatic neat poly(butylene succinate) (PBS) and poly(butylene succinate-co-neopentyl glycol succinate) (P(BS-co-NPGS)) copolyesters with different 1,4-butanediol/neopentyl glycol ratios were synthesized through a two-step process of transesterification and polycondensation using stannous chloride and 4-Methylbenzenesulfonic acid as the co-catalysts. The structure, non-isothermal crystallization behavior, crystalline morphology and crystal structure of neat PBS and P(BS-co-NPGS) copolyesters were characterized by (1)H NMR, differential scanning calorimetry (DSC), polarized optical microscope (POM) and wide angle X-ray diffraction (WAXD), respectively. The Avrami equation modified by Jeziorny and Mo's method was employed to describe the non-isothermal crystallization kinetics of the neat PBS and its copolyesters. The modified Avrami equation could adequately describe the primary stage of non-isothermal crystallization kinetics of the neat PBS and its copolyesters. Mo's method provided a fairly satisfactory description of the non-isothermal crystallization of neat PBS and its copolyesters. Interestingly, the values of 1/t1/2, Zc and F(T) obtained by the modified Avrami equation and Mo's method analysis indicated that the crystallization rate increased first and then decreased with an increase of NPGS content compared that of neat PBS, whereas the crystallization mechanism almost kept unchanged. The results of tensile testing showed that the ductility of PBS was largely improved by incorporating NPGS units. The elongation at break increased remarkably with increasing NPGS content. In particular, the sample with 20% NPGS content showed around 548% elongation at break. PMID:25491999

  1. Degradation studies of 1, 6-diisocyanatohexane-extended poly (1, 4-butylene succinate) - bioactive glass scaffolds for bone tissue repair applications

    Science.gov (United States)

    Kaur, Kulwinder; Singh, K. J.; Anand, Vikas

    2016-05-01

    Bio composite scaffolds prepared from polymer and bio glass provide necessary sites for bone tissue regeneration. In the presented work, bioactive glass scaffolds have been prepared from 1, 6-diisocyanatohexane-extended poly (1, 4-butylene succinate) with different amount of bioactive glass powder by solvent casting method. Prepared scaffolds have been characterized by XRD, FTIR and FESEM techniques. Effect of content of bioactive glass on biodegradability has been investigated in detail.

  2. Enhancement of Mechanical and Thermal Properties of Oil Palm Empty Fruit Bunch Fiber Poly(butylene adipate-co-terephtalate) Biocomposites by Matrix Esterification Using Succinic Anhydride

    OpenAIRE

    Samira Siyamak; Nor Azowa Ibrahim; Sanaz Abdolmohammadi; Wan Md Zin Bin Wan Yunus; Mohamad Zaki AB Rahman

    2012-01-01

    In this work, the oil palm empty fruit bunch (EFB) fiber was used as a source of lignocellulosic filler to fabricate a novel type of cost effective biodegradable composite, based on the aliphatic aromatic co-polyester poly(butylene adipate-co-terephtalate) PBAT (EcoflexTM), as a fully biodegradable thermoplastic polymer matrix. The aim of this research was to improve the new biocomposites’ performance by chemical modification using succinic anhydride (SAH) as a coupling agent in the presence ...

  3. Effect of Fiber Esterification on Fundamental Properties of Oil Palm Empty Fruit Bunch Fiber/Poly(butylene adipate-co-terephthalate) Biocomposites

    OpenAIRE

    Mohamad Zaki AB Rahman; Wan Md Zin Wan Yunus; Nor Azowa Ibrahim; Sanaz Abdolmohammadi; Samira Siyamak

    2012-01-01

    A new class of biocomposites based on oil palm empty fruit bunch fiber and poly(butylene adipate-co-terephthalate) (PBAT), which is a biodegradable aliphatic aromatic co-polyester, were prepared using melt blending technique. The composites were prepared at various fiber contents of 10, 20, 30, 40 and 50 wt% and characterized. Chemical treatment of oil palm empty fruit bunch (EFB) fiber was successfully done by grafting succinic anhydride (SAH) onto the EFB fiber surface, and the modified fib...

  4. Non-isothermal crystallization kinetics and characterization of biodegradable poly(butylene succinate-co-neopentyl glycol succinate) copolyesters

    Energy Technology Data Exchange (ETDEWEB)

    Xie, Wen-Jie; Zhou, Xiao-Ming, E-mail: xiaomingzhou@tust.edu.cn

    2015-01-01

    Both biodegradable aliphatic neat poly(butylene succinate) (PBS) and poly(butylene succinate-co-neopentyl glycol succinate) (P(BS-co-NPGS)) copolyesters with different 1,4-butanediol/neopentyl glycol ratios were synthesized through a two-step process of transesterification and polycondensation using stannous chloride and 4-Methylbenzenesulfonic acid as the co-catalysts. The structure, non-isothermal crystallization behavior, crystalline morphology and crystal structure of neat PBS and P(BS-co-NPGS) copolyesters were characterized by {sup 1}H NMR, differential scanning calorimetry (DSC), polarized optical microscope (POM) and wide angle X-ray diffraction (WAXD), respectively. The Avrami equation modified by Jeziorny and Mo's method was employed to describe the non-isothermal crystallization kinetics of the neat PBS and its copolyesters. The modified Avrami equation could adequately describe the primary stage of non-isothermal crystallization kinetics of the neat PBS and its copolyesters. Mo's method provided a fairly satisfactory description of the non-isothermal crystallization of neat PBS and its copolyesters. Interestingly, the values of 1/t{sub 1/2}, Z{sub c} and F(T) obtained by the modified Avrami equation and Mo's method analysis indicated that the crystallization rate increased first and then decreased with an increase of NPGS content compared that of neat PBS, whereas the crystallization mechanism almost kept unchanged. The results of tensile testing showed that the ductility of PBS was largely improved by incorporating NPGS units. The elongation at break increased remarkably with increasing NPGS content. In particular, the sample with 20% NPGS content showed around 548% elongation at break. - Highlights: • The incorporation of NPGS units reduced the spherulite size of BS unit. • The existence of NPGS units did not change the crystal structure of BS unit. • The NPGS units incorporated in PBS could significantly improve the ductility of

  5. Production and characterization of novel starch and poly(butylene adipate-co-terephthalate)-based materials and their applications

    Science.gov (United States)

    Stagner, Jacqueline Ann

    This work focuses on the production and characterization of blends of maleated thermoplastic starch (MTPS) and poly(butylenes adipate-co-terephthalate) and their application for use as thermoformed objects, films, and foams. First, by the production and characterization of maleated thermoplastic starch (MTPS) synthesized by reactive extrusion in a twin-screw extruder, a better understanding of MTPS was gained. This reactive thermoplastic starch was prepared with glycerol as the plasticizer, maleic anhydride (MA), and free-radical initiator, 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane (Luperox 101). Dynamic light scattering (DLS), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), soxhlet extraction in acetone, and environmental scanning electron microscopy (ESEM) were performed to determine the effect of maleation, extrusion temperature, initiator concentration, and maleic anhydride concentration on the resulting MTPS. Next, maleated thermoplastic starch (MTPS) and thermoplastic starch (TPS) were reactively blended in a twin-screw extruder with a biodegradable polyester, poly(butylene adipate-co-terephthalate) (PBAT). The blends were extruded to produce thermoformable sheets. The mechanical properties of the sheets were characterized by tensile and puncture tests. Proof of grafting was determined by soxhlet extraction in dichloromethane and FTIR analysis. Observations of the thermal properties were made using DSC, while the surface of the sheets was imaged using ESEM. Blends of MTPS and PBAT were also extruded to produce films. Mechanical testing (tensile and puncture tests) and barrier performance testing (carbon dioxide, oxygen, and water vapor permeability) were performed on the films. Transmission electron microscopy (TEM) was used to image the blends and to view the dispersion of the various phases. Finally, blends of MTPS and PBAT were extruded with an endothermic chemical blowing agent to produce foams. The foams were

  6. The influence of manganese-cobalt oxide/graphene on reducing fire hazards of poly(butylene terephthalate).

    Science.gov (United States)

    Wang, Dong; Zhang, Qiangjun; Zhou, Keqing; Yang, Wei; Hu, Yuan; Gong, Xinglong

    2014-08-15

    By means of direct nucleation and growth on the surface of graphene and element doping of cobalt oxide (Co3O4) nano-particles, manganese-cobalt oxide/graphene hybrids (MnCo2O4-GNS) were synthesized to reduce fire hazards of poly(butylene terephthalate) (PBT). The structure, elemental composition and morphology of the obtained hybrids were surveyed by X-ray diffraction, X-ray photoelectron spectrometer and transmission electron microscopy, respectively. Thermogravimetric analysis was applied to simulate and study the influence of MnCo2O4-GNS hybrids on thermal degradation of PBT during combustion. The fire hazards of PBT and its composites were assessed by the cone calorimeter. The cone test results had showed that peak HRR and SPR values of MnCo2O4-GNS/PBT composites were lower than that of pure PBT and Co3O4-GNS/PBT composites. Furthermore, the incorporation of MnCo2O4-GNS hybrids gave rise to apparent decrease of pyrolysis products containing aromatic compounds, carbonyl compounds, carbon monoxide and carbon dioxide, attributed to combined impact of physical barrier for graphene and cat O4 for organic volatiles and carbon monoxide.

  7. Preparation and Properties of a New Type of Poly (butylene-terephthalate) with Layered Silicate Nanocomposites

    Institute of Scientific and Technical Information of China (English)

    柯扬船

    2003-01-01

    In this paper, poly(butylene-terephthalate)-layered silicate of clay nanocomposites (NPBT) are reported. Their thermal properties, heat distortion temperature (HDT) and crystallization nucleation are investigated. NPBT samples have apparent viscosity over 0.85, HDT of 30℃ to 50℃ higher than that of poly (butyleneterephthalate) (PBT) for clay load from 1.0% to 10.0% (by mass), and higher capability to accommodate clay than other polymers. The nonisothermal crystallization experiments indicate that the better thermal degradation behavior and crystallization rate of NPBT are 50% higher than PBT, and its injection mould processing temperature is lowered from ll0℃ to 55℃. NPBT samples are characterized by several techniques. X-ray shows an original clay interlayer distance enlarged from 1.0 nm to 2.5 nm, while both TEM and AFM indicate an average size from 30nm to 100nm of exfoliated clay layers, and 3%(by mass) of particle agglomeration being phase separated from PBT matrix, which are factors on some mechanical properties decrease of NPBT. The disappearance of spherulitic morphology in NPBT resulted from layers nucleation is detected. Improving NPBT properties by treating clay with long chain organic reagent and controlling the way to load it is suggested.

  8. Biological denitrification using poly(butylene succinate) as carbon source and biofilm carrier for recirculating aquaculture system effluent treatment.

    Science.gov (United States)

    Zhu, Song-Ming; Deng, Ya-Le; Ruan, Yun-Jie; Guo, Xi-Shan; Shi, Ming-Ming; Shen, Jia-Zheng

    2015-09-01

    Nitrate removal is essential for the sustainable operation of recirculating aquaculture system (RAS). This study evaluated the heterotrophic denitrification using poly(butylene succinate) as carbon source and biofilm carrier for RAS wastewater treatment. The effect of varied operational conditions (influent type, salinity and nitrate loading) on reactor performance and microbial community was investigated. The high denitrification rates of 0.53 ± 0.19 kg NO3(-)-N m(-3) d(-1) (salinity, 0‰) and 0.66 ± 0.12 kg NO3(-)-Nm(-3) d(-1) (salinity, 25‰) were achieved, and nitrite concentration was maintained below 1mg/L. In addition, the existence of salinity exhibited more stable nitrate removal efficiency, but caused adverse effects such as excessive effluent dissolved organic carbon (DOC) and dissimilation nitrate reduce to ammonia (DNRA) activity. The degradation of PBS was further confirmed by SEM and FTIR analysis. Illumina sequencing revealed the abundance and species changes of functional denitrification and degradation microflora which might be the primary cause of varied reactor performance. PMID:26093254

  9. The influence of manganese-cobalt oxide/graphene on reducing fire hazards of poly(butylene terephthalate).

    Science.gov (United States)

    Wang, Dong; Zhang, Qiangjun; Zhou, Keqing; Yang, Wei; Hu, Yuan; Gong, Xinglong

    2014-08-15

    By means of direct nucleation and growth on the surface of graphene and element doping of cobalt oxide (Co3O4) nano-particles, manganese-cobalt oxide/graphene hybrids (MnCo2O4-GNS) were synthesized to reduce fire hazards of poly(butylene terephthalate) (PBT). The structure, elemental composition and morphology of the obtained hybrids were surveyed by X-ray diffraction, X-ray photoelectron spectrometer and transmission electron microscopy, respectively. Thermogravimetric analysis was applied to simulate and study the influence of MnCo2O4-GNS hybrids on thermal degradation of PBT during combustion. The fire hazards of PBT and its composites were assessed by the cone calorimeter. The cone test results had showed that peak HRR and SPR values of MnCo2O4-GNS/PBT composites were lower than that of pure PBT and Co3O4-GNS/PBT composites. Furthermore, the incorporation of MnCo2O4-GNS hybrids gave rise to apparent decrease of pyrolysis products containing aromatic compounds, carbonyl compounds, carbon monoxide and carbon dioxide, attributed to combined impact of physical barrier for graphene and cat O4 for organic volatiles and carbon monoxide. PMID:24997255

  10. Poly(lactide-g-poly(butylene succinate-co-adipate with High Crystallization Capacity and Migration Resistance

    Directory of Open Access Journals (Sweden)

    Xi Yang

    2016-04-01

    Full Text Available Plasticized polylactide (PLA with increased crystallization ability and prolonged life-span in practical applications due to the minimal plasticizer migration was prepared. Branched plasticized PLA was successfully obtained by coupling poly(butylene succinate-co-adipate (PBSA to crotonic acid (CA functionalized PLA. The plasticization behavior of PBSA coupled PLA (PLA-CA-PBSA and its counterpart PBSA blended PLA (PLA/PBSA were fully elucidated. For both PLA-CA-PBSA and PLA/PBSA, a decrease of Tg to around room temperature and an increase in the elongation at break of PLA from 14% to 165% and 460%, respectively, were determined. The crystallinity was increased from 2.1% to 8.4% for PLA/PBSA and even more, to 10.6%, for PLA-CA-PBSA. Due to the inherent poor miscibility between the PBSA and PLA, phase separation occurred in the blend, while PLA-CA-PBSA showed no phase separation which, together with the higher crystallinity, led to better oxygen barrier properties compared to neat PLA and PLA/PBSA. A higher resistance to migration during hydrolytic degradation for the PLA-CA-PBSA compared to the PLA/PBSA indicated that the plasticization effect of PBSA in the coupled material would be retained for a longer time period.

  11. Simultaneous ammonia and nitrate removal in an airlift reactor using poly(butylene succinate) as carbon source and biofilm carrier.

    Science.gov (United States)

    Ruan, Yun-Jie; Deng, Ya-Le; Guo, Xi-Shan; Timmons, Michael B; Lu, Hui-Feng; Han, Zhi-Ying; Ye, Zhang-Ying; Shi, Ming-Ming; Zhu, Song-Ming

    2016-09-01

    In this study, an airlift inner-loop sequencing batch reactor using poly(butylene succinate) as the biofilm carrier and carbon source was operated under an alternant aerobic/anoxic strategy for nitrogen removal in recirculating aquaculture system. The average TAN and nitrate removal rates of 47.35±15.62gNH4-Nm(-3)d(-1) and 0.64±0.14kgNO3-Nm(-3)d(-1) were achieved with no obvious nitrite accumulation (0.70±0.76mg/L) and the dissolved organic carbon in effluents was maintained at 148.38±39.06mg/L. Besides, the activities of dissimilatory nitrate reduction to ammonium and sulfate reduction activities were successfully inhibited. The proteome KEGG analysis illustrated that ammonia might be removed through heterotrophic nitrification, while the activities of nitrate and nitrite reductases were enhanced through aeration treatment. The microbial community analysis revealed that denitrifiers of Azoarcus and Simplicispira occupied the dominate abundance which accounted for the high nitrate removal performance. Overall, this study broadened our understanding of simultaneous nitrification and denitrification using biodegradable material as biofilm carrier. PMID:27343453

  12. Crystallization behavior and thermal stability of poly(butylene succinate)/poly(propylene carbonate) blends prepared by novel vane extruder

    Science.gov (United States)

    Chen, Rongyuan; Zou, Wei; Zhang, Haichen; Zhang, Guizhen; Qu, Jinping

    2016-03-01

    This work focused on the study of crystallization behavior and thermal stability of degradable poly(butylene succinate) (PBS) and poly(propylene carbonate) (PPC) blends prepared by vane extruder based on elongation force field, which is novel equipment for polymer processing. Dicumyl peroxide (DCP) was applied in this work as compatibilizer for PBS/PPC blend. Crystallization behavior and melting behavior of the blends were investigated by differential scanning calorimetry (DSC) testing. Thermal stability of the blends was studied by thermogravimetric (TG) testing. Furthermore, the melt flow indices (MFI) of the blends were examined by a MFI instrument. The results showed that the crystallization temperature of PBS decreased with the addition of PPC and DCP. The glass transition temperature of PPC increased and the melting temperature of the blend increased with the addition of PPC and DCP, which indicated that the entanglement between the molecular chains of PBS and PPC was enhanced. Thermogravimetric analysis showed that a two-step decomposition process of the blend occurred due to the different thermal resistance of PBS and PPC, and the addition of PBS reduced the decomposition rate of PPC. Moreover, the addition of PBS improved the melt flow property of PPC.

  13. Fabrication of Chitin/Poly(butylene succinate/Chondroitin Sulfate Nanoparticles Ternary Composite Hydrogel Scaffold for Skin Tissue Engineering

    Directory of Open Access Journals (Sweden)

    S. Deepthi

    2014-12-01

    Full Text Available Skin loss is one of the oldest and still not totally resolved problems in the medical field. Since spontaneous healing of the dermal defects would not occur, the regeneration of full thickness of skin requires skin substitutes. Tissue engineering constructs would provide a three dimensional matrix for the reconstruction of skin tissue and the repair of damage. The aim of the present work is to develop a chitin based scaffold, by blending it with poly(butylene succinate (PBS, an aliphatic, biodegradable and biocompatible synthetic polymer with excellent mechanical properties. The presence of chondroitin sulfate nanoparticles (CSnp in the scaffold would favor cell adhesion. A chitin/PBS/CSnp composite hydrogel scaffold was developed and characterized by SEM (Scanning Electron Microscope, FTIR (Fourier Transform Infrared Spectroscopy, and swelling ratio of scaffolds were analyzed. The scaffolds were evaluated for the suitability for skin tissue engineering application by cytotoxicity, cell attachment, and cell proliferation studies using human dermal fibroblasts (HDF. The cytotoxicity and cell proliferation studies using HDF confirm the suitability of the scaffold for skin regeneration. In short, these results show promising applicability of the developed chitin/PBS/CSnps ternary composite hydrogel scaffolds for skin tissue regeneration.

  14. Preparation and characterization of crosslinked poly(butylene adipate-co-terephthalate)/polyhedral oligomeric silsesquioxane nanocomposite by electron beam irradiation

    International Nuclear Information System (INIS)

    The electron beam-induced crosslinking of poly(butylene adipate-co-terephthalate) (PBAT)/polyhedral oligomeric silsesquioxane (POSS) nanocomposites was investigated in this study. PBAT/POSS nanocomposites prepared by a solution blending with various compositions were crosslinked by electron beam irradiation at various absorbed doses ranging from 20 to 200 kGy and their properties were characterized in terms of their degree of crosslinking, morphology, thermal and mechanical properties, and biodegradability. The results of the degree of crosslinking measurements revealed that PBAT/POSS nanocomposites were more effectively crosslinked than the pure PBAT and that the degree of crosslinking was dependent on the absorbed dose and POSS content. From the results of the FE-SEM and EDX analyses, the POSS was found to be uniformly dispersed in the PBAT matrix. Based on the results of the UTM, DMA, and TMA, the crosslinked PBAT/POSS nanocomposites exhibited much higher thermal and mechanical properties compared to those of the pure PBAT. - Highlights: ► Crosslinked PBAT/POSS nanocomposites were prepared by electron beam irradiation. ► The POSS as a nanofillers was homogeneously dispersed in the PBAT matrix. ► The crosslinked nanocomposites exhibited improved thermal and mechanical properties.

  15. Toughening of biodegradable polylactide/poly(butylene succinate-co-adipate) blends via in situ reactive compatibilization.

    Science.gov (United States)

    Ojijo, Vincent; Ray, Suprakas Sinha; Sadiku, Rotimi

    2013-05-22

    Polylactide and poly(butylene succinate-co-adipate) (PLA/PBSA) were melt-blended in the presence of triphenyl phosphite (TPP). An increase in the torque during melt mixing was used to monitor the changes in viscosity as compatibilization of the blends occurred. Scanning electron micrographs showed not only a reduction in the dispersed-phase size with increased TPP content but also fibrillated links between the PLA and PBSA phases, signifying compatibilization. Moreover, optimization of parameters such as the mixing sequence and time, TPP content, and PBSA concentration revealed that blends containing 30 and 10 wt % PBSA and 2 wt % TPP, which were processed for 30 min, were optimal in terms of thermomechanical properties. The impact strength increased from 6 kJ/m(2) for PLA to 11 and 16 kJ/m(2) for blends containing 30 and 10 wt % PBSA, respectively, whereas the elongation-at-break increased from 6% for PLA to 20 and 37% for blends containing 30 and 10 wt % PBSA, respectively. Upon compatibilization, the failure mode shifted from the brittle fracture of PLA to ductile deformation, effected by the debonding between the two phases. With improved phase adhesion, compatibilized blends not only were toughened but also did not significantly lose tensile strength and thermal stability.

  16. Phase Morphology and Mechanical Properties of Cyclic Butylene Terephthalate Oligomer-Containing Rubbers: Effect of Mixing Temperature

    Directory of Open Access Journals (Sweden)

    István Zoltán Halász

    2016-08-01

    Full Text Available In this work, the effect of mixing temperature (Tmix on the mechanical, rheological, and morphological properties of rubber/cyclic butylene terephthalate (CBT oligomer compounds was studied. Apolar (styrene butadiene rubber, SBR and polar (acrylonitrile butadiene rubber, NBR rubbers were modified by CBT (20 phr for reinforcement and viscosity reduction. The mechanical properties were determined in tensile, tear, and dynamical mechanical analysis (DMTA tests. The CBT-caused viscosity changes were assessed by parallel-plate rheometry. The morphology was studied by scanning electron microscopy (SEM. CBT became better dispersed in the rubber matrices with elevated mixing temperatures (at which CBT was in partially molten state, which resulted in improved tensile properties. With increasing mixing temperature the size of the CBT particles in the compounds decreased significantly, from few hundred microns to 5–10 microns. Compounding at temperatures above 120 °C and 140 °C for NBR and SBR, respectively, yielded reduced tensile mechanical properties most likely due to the degradation of the base rubber. The viscosity reduction by CBT was more pronounced in mixes with coarser CBT dispersions prepared at lower mixing temperatures.

  17. Morphology and mechanical properties of poly(butylene adipate-co-terephthalate)/potato starch blends in the presence of synthesized reactive compatibilizer or modified poly(butylene adipate-co-terephthalate).

    Science.gov (United States)

    Wei, Dafu; Wang, Hao; Xiao, Huining; Zheng, Anna; Yang, Yang

    2015-06-01

    The biodegradable poly(butylene adipate-co-terephthalate)(PBAT)/thermoplastic starch (TPS) composite has received considerable attention because of the environmental concerns raised by solid waste disposal. However, the application of PBAT/TPS blends was limited due to the poor mechanical properties originating from the incompatibility between PBAT and TPS. In this work, two approaches were developed to improve the mechanical properties of PBAT/TPS blends. One approach is to use compatibilizers, including the synthesized reactive compatibilizer - a styrene-maleic anhydride-glycidyl methacrylate (SMG) terpolymer, and the commercial compatibilizer (Joncryl-ADR-4368). The chemical structures of SMG were analyzed with (1)H NMR and FT-IR. The other approach is to use the modified PBAT (M-PBAT) to replace part of PBAT in the PBAT/TPS blends. M-PBATs with higher molecular weight were obtained via reactive extrusion of PBAT in the presence of a chain extender. The better dispersion of TPS in PBAT was observed in SEM images when using M-PBAT, leading to the higher tensile strength and elongation at break of PBAT/TPS blends. However, the elongation at break decreased in the presence of compatibilizer (SMG or 4368), though the tensile strength remained in a similar level or slightly higher. Overall, the tensile strength and the elongation at break of the resulting biodegradable PBAT/M-PBAT/TPS blends (TPS=40wt%) were above 27.0MPa and 500%, respectively, which is promising for various applications, including packaging and agricultural mulching films.

  18. Surface modification of poly(styrene-b-(ethylene-co-butylene)-b-styrene) elastomer via photo-initiated graft polymerization of poly(ethylene glycol)

    Science.gov (United States)

    Li, Xiaomeng; Luan, Shifang; Yang, Huawei; Shi, Hengchong; Zhao, Jie; Jin, Jing; Yin, Jinghua; Stagnaro, Paola

    2012-01-01

    Poly(styrene-b-(ethylene-co-butylene)-b-styrene) (SEBS) copolymer biomedical elastomer was covalently grafted with poly(ethylene glycol) methyl ether methacrylate (PEGMA) via a photo-initiated graft polymerization technique. The surface graft polymerization of SEBS with PEGMA was verified by ATR-FTIR and XPS. Effect of graft polymerization parameters, i.e., monomer concentration, UV irradiation time and initiator concentration on the grafting density was investigated. Comparing with the virgin SEBS film, the PEGMA-modified SEBS film presented an enhanced wettability and a larger surface energy. Besides, the surface grafting of PEGMA imparted excellent anti-platelet adhesion and anti-protein adsorption to the SEBS surface.

  19. THERMAL PROPERTY, MISCIBILITY AND CRYSTALLIZATION BEHAVIOR OF POLY(3-HYDROXYBUTYRATE-co 3-YDROXYHEXANOATE) AND POLY(BUTYLENE SUCCINATE-ADIPATE) (PHBHHX/PBSA) BLENDS

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    Blends of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHHx) and poly(butylene succinate-adipate) (PBSA), both biodegradable semicrystalline polyesters, were prepared with the ratio of PHBHHx/PBSA ranging from 80/20 to 20/80 by melt mixing method. Differential scanning calorimetry (DSC), thermogravimetry analysis (TGA), dynamic mechanical thermal analysis (DMA), polarizing optical microscopy (POM) and wide angle X-ray diffractometer (WAXD) were used to study the miscibility and crystallization behavior of PHBHHx/PBSA blends. Experimental results indicate that PHBHHx is immiscible with PBSA as shown by the almost unchanged glass transition temperature and the biphasic melt.

  20. Surface modification of poly(styrene-b-(ethylene-co-butylene)-b-styrene) elastomer via photo-initiated graft polymerization of poly(ethylene glycol)

    Energy Technology Data Exchange (ETDEWEB)

    Li Xiaomeng [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Luan Shifang, E-mail: sfluan@ciac.jl.cn [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Yang Huawei; Shi Hengchong; Zhao Jie; Jin Jing [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Yin Jinghua, E-mail: yinjh@ciac.jl.cn [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Stagnaro, Paola [Istituto per Io Studio delle Macromolecole, Consiglio Nazionale delle Ricerche, Via de Marini 6, 16149 Genova (Italy)

    2012-01-15

    Poly(styrene-b-(ethylene-co-butylene)-b-styrene) (SEBS) copolymer biomedical elastomer was covalently grafted with poly(ethylene glycol) methyl ether methacrylate (PEGMA) via a photo-initiated graft polymerization technique. The surface graft polymerization of SEBS with PEGMA was verified by ATR-FTIR and XPS. Effect of graft polymerization parameters, i.e., monomer concentration, UV irradiation time and initiator concentration on the grafting density was investigated. Comparing with the virgin SEBS film, the PEGMA-modified SEBS film presented an enhanced wettability and a larger surface energy. Besides, the surface grafting of PEGMA imparted excellent anti-platelet adhesion and anti-protein adsorption to the SEBS surface.

  1. The effect of epoxidized soybean oil on mechanical and rheological properties of poly(butylene succinate)/lignin via vane extruder

    Science.gov (United States)

    Liu, Huanyu; Huang, Zhaoxia; Qu, Jinping; Meng, Cong

    2016-03-01

    Epoxidized Soybean Oil (ESO) have been used as the compatilizer in the Poly (butylene succinate)/lignin (PBS/lignin) composites. Compatibilized composites were fabricated by a novel vane extruder (VE) which can generate global and dynamic elongational flow. The effects of ESO on the mechanical, rheological properties and morphology of PBS/lignin were studied. The results indicated that the use of ESO had plasticizing effect on the matrix PBS while the addition reduced tensile strength. From SEM micrographs it could be clearly observed that there was a better interfacial adhesion between lignin and matrix. Meanwhile, rheological tests showed the incorporation of ESO improved its Newtonian behavior and can enhance PBS's flexibility.

  2. Ionic polymer-metal composite actuators employing sulfonated poly (styrene-ethylene-butylene-styrene) as ionic-exchange membranes

    Science.gov (United States)

    Wang, Xuan-Lun; Oh, Il-Kwon; Lu, Jun; Ju, Jin-Hun; Lee, Sun-Woo

    2007-07-01

    There is growing interest in biomimetic motions by employing ionic polymer-metal composites (IPMCs) as the candidates for the fabrication of artificial muscle. However, the membrane materials currently used in IPMC actuators have been limited to a few commercially available perfluorinated ionic polymers, such as Nafion, and they suffer from several shortcomings among which their high cost presents a major obstacle for wide application. With excellent proton conductivity and high water uptake capacity, commercially available Sulfonated poly (styrene-ethylene-butylene-styrene) (SEBS) of low cost has been investigated for many years as a fuel cell membrane. Herein, we report the preparation of a novel IPMC actuator based on the sulfonated SEBS (SSEBS) membrane. The platinum electrodes of the SEBS actuators were obtained with electroless plating procedure, and the cation exchange with lithium was performed by soaking the composite membranes into a 1.5N LiCl solution. The surface and cross-sectional morphologies of the SSEBS actuators were observed by using scanning electron microscopy (SEM), which revealed that the platinum layer up to 8µm was deposited on the top and bottom surfaces of the SSEBS membrane. The electromechanical bending responses were investigated under alternating current excitations with various driving frequencies and voltage amplitudes, which showed high electrical strains under sinusoidal signal. The effect of the membrane thickness on the performance of the actuators was also addressed in this presentation. This kind of IPMC has great potentials for the applications in biomimetic sensors and actuators, which can be utilized to mimic the locomotion of fish and insects and can be applied to micro-robots and bio-medical devices as well.

  3. Reinforcement effect of poly(butylene succinate) (PBS)-grafted cellulose nanocrystal on toughened PBS/polylactic acid blends.

    Science.gov (United States)

    Zhang, Xuzhen; Zhang, Yong

    2016-04-20

    Poly(butylene succinate) (PBS)/polylactic acid (PLA) blends modified with dicumyl peroxide (DCP) were reinforced by PBS-g-cellulose nanocrystal (CNC) through melt mixing. PBS-g-CNC was prepared through in situ polymerization and its structure was confirmed by FTIR, (13)C NMR, XPS and GPC analysis after saponification. The morphological analysis of PBS/PLA/PBS-g-CNC composites before and after etched by CH2Cl2 shows that the addition of DCP and PBS-g-CNC could decrease the size of PBS as a dispersed phase in PLA matrix and improve the dispersion of PBS-g-CNC in both PBS and PLA phases, which could affect the crystallization and mechanical properties of composites. The crystallinity of PLA α'-phase crystal in PBS/PLA/PBS-g-CNC composites is increased obviously by the addition of PBS-g-CNC, leading to an increase of the crystallinity of the composites. PBS/PLA blends modified by DCP have high Notched Izod impact strength and moduli, and the values are increased by the addition of PBS-g-CNC. Both storage modulus and glass translation temperature of PBS/PLA blend are increased by DCP and PBS-g-CNC, which is proved by DMA results, showing a weak molecular segment mobility of PBS/PLA matrix. The addition of DCP decreases the crystallization temperature and crystallinity of PBS/PLA composite, but increases the thermal stability of composites, mostly because of the crosslink effect of DCP on PBS/PLA matrix.

  4. Reinforcement effect of poly(butylene succinate) (PBS)-grafted cellulose nanocrystal on toughened PBS/polylactic acid blends.

    Science.gov (United States)

    Zhang, Xuzhen; Zhang, Yong

    2016-04-20

    Poly(butylene succinate) (PBS)/polylactic acid (PLA) blends modified with dicumyl peroxide (DCP) were reinforced by PBS-g-cellulose nanocrystal (CNC) through melt mixing. PBS-g-CNC was prepared through in situ polymerization and its structure was confirmed by FTIR, (13)C NMR, XPS and GPC analysis after saponification. The morphological analysis of PBS/PLA/PBS-g-CNC composites before and after etched by CH2Cl2 shows that the addition of DCP and PBS-g-CNC could decrease the size of PBS as a dispersed phase in PLA matrix and improve the dispersion of PBS-g-CNC in both PBS and PLA phases, which could affect the crystallization and mechanical properties of composites. The crystallinity of PLA α'-phase crystal in PBS/PLA/PBS-g-CNC composites is increased obviously by the addition of PBS-g-CNC, leading to an increase of the crystallinity of the composites. PBS/PLA blends modified by DCP have high Notched Izod impact strength and moduli, and the values are increased by the addition of PBS-g-CNC. Both storage modulus and glass translation temperature of PBS/PLA blend are increased by DCP and PBS-g-CNC, which is proved by DMA results, showing a weak molecular segment mobility of PBS/PLA matrix. The addition of DCP decreases the crystallization temperature and crystallinity of PBS/PLA composite, but increases the thermal stability of composites, mostly because of the crosslink effect of DCP on PBS/PLA matrix. PMID:26876864

  5. Biocompatibility and drug release behavior of scaffolds prepared by coaxial electrospinning of poly(butylene succinate) and polyethylene glycol

    Energy Technology Data Exchange (ETDEWEB)

    Llorens, E.; Ibañez, H. [Departament d' Enginyeria Química, Universitat Politècnica de Catalunya, Av. Diagonal 647, Barcelona E-08028 (Spain); Valle, L.J. del, E-mail: luis.javier.del.valle@upc.edu [Departament d' Enginyeria Química, Universitat Politècnica de Catalunya, Av. Diagonal 647, Barcelona E-08028 (Spain); Puiggalí, J. [Departament d' Enginyeria Química, Universitat Politècnica de Catalunya, Av. Diagonal 647, Barcelona E-08028 (Spain); Center for Research in Nano-Engineering (CrNE), Universitat Politècnica de Catalunya, Edifici C, C/Pasqual i Vila s/n, Barcelona E-08028 (Spain)

    2015-04-01

    Scaffolds constituted by electrospun microfibers of poly(ethylene glycol) (PEG) and poly(butylene succinate) (PBS) were studied. Specifically, coaxial microfibers having different core–shell distributions and compositions were considered as well as uniaxial micro/nanofibers prepared from mixtures of both polymers. Processing conditions were optimized for all geometries and compositions and resulting morphologies (i.e. diameter and surface texture) characterized by scanning electron microscopy. Chemical composition, molecular interactions and thermal properties were evaluated by FTIR, NMR, XPS and differential scanning calorimetry. The PEG component of electrospun fibers could be solubilized by immersion of scaffolds in aqueous medium, giving rise to high porosity and hydrophobic samples. Nevertheless, a small amount of PEG was retained in the PBS matrix, suggesting some degree of mixing. Solubilization was slightly dependent on fiber structure; specifically, the distribution of PEG in the core or shell of coaxial fibers led to higher or lower retention levels, respectively. Scaffolds could be effectively loaded with hydrophobic drugs having antibacterial and anticarcinogenic activities like triclosan and curcumin, respectively. Their release was highly dependent on their chemical structure and medium composition. Thus, low and high release rates were observed in phosphate buffer saline (SS) and SS/ethanol (30:70 v/v), respectively. Slight differences in the release of triclosan were found depending on fiber distribution and composition. Antibacterial activity and biocompatibility were evaluated for both loaded and unloaded scaffolds. - Highlights: • Coaxial microfibers with different hydrophobicities were studied. • The surface morphology of the coaxial fiber shows the distribution of polymers. • Coaxial fiber microstructure favors the polymer molecular orientation. • These hybrid materials have greater advantages for loading and drug release. • PEG

  6. IPA改性PBT共聚酯结晶性能研究%Studies on crystallization behavior of poly(butylene terephthalate-co-isophthalate)

    Institute of Scientific and Technical Information of China (English)

    张军; 张建; 李红芳

    2012-01-01

    Poly(butylene terephthalate)(PBT) is an important semi-crystallization thermoplastic polyester.Various uses of PBT require different crystallization characteristic.In this papers some samples of Poly(butylene terephthalate-co-isophthalate) with 0~20% isophthalate units contents have been prepared and their crystallization property has been analyzed by using DSC.The result shows that the crystallization melting temperature and melting enthalpy of copolyester reduces approximate-linearly with increasing of isophthalate unit content.%聚对苯二甲酸丁二醇酯(PBT)是重要的半结晶性热塑性聚酯,差别化的聚酯产品需要差别化的结晶性能。文章合成得到间苯二甲酸(IPA)含量0~20%改性PBT共聚酯样品,DSC分析表明改性共聚酯的结晶熔点及结晶熔融焓下降,且随IPA含量的增加近似呈线性减小。

  7. Effect of rare earth hypophosphite and melamine cyanurate on fire performance of glass-fiber reinforced poly(1,4-butylene terephthalate) composites

    International Nuclear Information System (INIS)

    Highlights: ► We synthesize and characterize two types of rare earth hypophosphite (REHP). ► REHP and melamine cyanurate are used as flame retardants. ► We prepare fire retarded glass-fiber/poly(1,4-butylene terephthalate) composites. ► The flammability of these composites is significantly reduced. - Abstract: This work mainly deals with a novel flame retardant system for glass-fiber reinforced poly(1,4-butylene terephthalate) (GRPBT) composites using trivalent rare earth hypophosphite (REHP) and melamine cyanurate (MC) through melt blending method. Firstly, two types of REHP, lanthanum hypophosphite and cerium hypophosphite, were synthesized and characterized. Thermal gravimetric analysis (TGA) was employed to investigate the thermal decomposition behavior of REHP and flame retardant treated GRPBT composites. Thermal combustion properties were measured using microscale combustion calorimeter. Fire performance was evaluated by limiting oxygen index, Underwriters Laboratories 94 and cone calorimeter. The results showed that the flammability of GRPBT is significantly reduced by the incorporation of the flame retardant mixture. Mechanism analysis revealed that the addition of MC reduces the condensed phase effect of REHP, but improves the flame inhibition in gas phase.

  8. The influence of antioxidant and post-synthetic treatment on the properties of biodegradable poly(butylene succinates modified with poly(propylene oxide

    Directory of Open Access Journals (Sweden)

    DRAGANA PEPIC

    2007-12-01

    Full Text Available Novel poly(ester–ethers based on poly(butylene succinate (PBS as the hard segments and 30 mass % of poly(propylene oxide (PPO as the soft segments were synthesized with varying amount of the antioxidant (N,N'-diphenyl-p-phenylenediamine, DPPD. The influences of the addition of DPPD and the impact of post-synthetic treatment by precipitation on the molecular structure, thermal and physical properties, as well as on the storage stability of the biodegradable aliphatic copolyesters, were investigated. The structure and composition of the copolymers were determined by means of 1H-NMR spectroscopy. The molecular weight and polydispersity of the poly(ester–ethers were evaluated from solution viscosity and GPC measurements. The thermal properties and stability were evaluated, respecttively, by means of DSC and non-isothermal thermogravimetry in an inert nitrogen atmosphere. The biodegradability potential of the polymers was studied in hydrolytic and enzymatic degradation tests with Candida cylindracea lipase by monitoring the weight loss of polymer films after incubation. The weight losses of the samples increased with time and were in the range from 1 to 5 mass % after 4 weeks. GPC analysis confirmed that there were changes in the molecular weight of the copolyesters during both hydrolytic and enzymatic degradation tests, leading to the conclusion that the degradation mechanism of poly(butylenes succinate modified with PPO occurred through surface erosion and bulk degradation.

  9. The influence of manganese–cobalt oxide/graphene on reducing fire hazards of poly(butylene terephthalate)

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Dong; Zhang, Qiangjun; Zhou, Keqing; Yang, Wei [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026 (China); Hu, Yuan, E-mail: yuanhu@ustc.edu.cn [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026 (China); USTC-CityU Joint Advanced Research Centre, Suzhou Key Laboratory of Urban Public Safety, Suzhou Institute for Advanced Study, University of Science and Technology of China, 166 Ren’ai Road, Suzhou, Jiangsu 215123 (China); Gong, Xinglong, E-mail: gongxl@ustc.edu.cn [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026 (China); CAS Key Laboratory of Mechanical Behaviour and Design of Materials, Department of Modern Mechanics, University of Science and Technology of China, Hefei, Anhui 230026 (China)

    2014-08-15

    Highlights: • MnCo{sub 2}O{sub 4}–GNS hybrids are synthesized by a two-stage liquid phase method. • MnCo{sub 2}O{sub 4}–GNS/PBT composites were prepared via a masterbatch-melt blending method. • Fire hazards are monitored and evaluated by cone calorimeter and TG-IR. • MnCo{sub 2}O{sub 4}–GNS hybrids decrease thermal hazards and smoke hazards of PBT composites. • MnCo{sub 2}O{sub 4}–GNS hybrids perform better catalytic oxidation of CO and organic volatile. - Abstract: By means of direct nucleation and growth on the surface of graphene and element doping of cobalt oxide (Co{sub 3}O{sub 4}) nano-particles, manganese–cobalt oxide/graphene hybrids (MnCo{sub 2}O{sub 4}–GNS) were synthesized to reduce fire hazards of poly(butylene terephthalate) (PBT). The structure, elemental composition and morphology of the obtained hybrids were surveyed by X-ray diffraction, X-ray photoelectron spectrometer and transmission electron microscopy, respectively. Thermogravimetric analysis was applied to simulate and study the influence of MnCo{sub 2}O{sub 4}–GNS hybrids on thermal degradation of PBT during combustion. The fire hazards of PBT and its composites were assessed by the cone calorimeter. The cone test results had showed that peak HRR and SPR values of MnCo{sub 2}O{sub 4}–GNS/PBT composites were lower than that of pure PBT and Co{sub 3}O{sub 4}–GNS/PBT composites. Furthermore, the incorporation of MnCo{sub 2}O{sub 4}–GNS hybrids gave rise to apparent decrease of pyrolysis products containing aromatic compounds, carbonyl compounds, carbon monoxide and carbon dioxide, attributed to combined impact of physical barrier for graphene and cat O{sub 4} for organic volatiles and carbon monoxide.

  10. STUDY ON PHOTO-DEGRADATION OF NEW PESTICIDE BUTYLENE FIPRONIL%新型农药丁烯氟虫腈的光降解研究

    Institute of Scientific and Technical Information of China (English)

    曹维强; 吕飞; 余优军; 吴云普; 佘永新; 王静

    2011-01-01

    为了解丁烯氟虫腈在液体中的降解趋势,采用液液萃取气相色谱-质谱(GC-MS)测定水中丁烯氟虫腈含量,研究丁烯氟虫腈在紫外光和太阳光照射下,在不同液体中的降解动态和降解产物.研究结果表明,在紫外光照射下,丁烯氟虫腈在水、0.01mol·L-1氯化钙溶液、甲醇、乙酸乙酯以及正己烷中的降解过程均符合一级反应动力学,27℃下丁烯氟虫腈溶液的降解半衰期分别为2.69 h、2.67h、6.30h、5.63 h和1.52 h,在丙酮中几乎不降解;丁烯氟虫腈在紫外光照射下的降解速率要快于在阳光照射下的降解速率,随着温度的升高,光解速率增加,随着pH值的增加或者降低,降解速率有所降低.采用气相色谱质谱仪对丁烯氟虫腈的3种光产物结构进行了初步鉴定,以期对丁烯氟虫腈的科学应用提供理论依据.%A method was developed for the determination of butylene fipronil residues in aqueous solution with liquid-liquid extraction and gas chromatography/mass spectrometry (C,C/MS) in order to investigate the photo-degradation dynamic of butylene fipronil in different solutions under ultraviolet(UV) light and sun light.The results of the study showed that the photo-degradation of butylene fipronil could be described by first-order kinetics in water, 0.01 mol. L-1CaCl2 solution, methanol, ethyl acetate and hexane under UV light. The half life of photo-degradation was 2.69 h,2.67 h,6.30 h,5.63 h and 1.52 h respectively at 27 ℃. But it hardly degraded in acetone. The effect of light source, temperature and pH value on degradation rate was also studied. The results showed that the photo-degradation rate under UV light was faster than that under sun light, photo-degradation rate were accelerated with temperature, but slowed when pH value was increased or decreased. Three photo-degradation products of butylene fipronil were indentified with (CC/MS).

  11. Surface modification of poly(styrene-b-(ethylene-co-butylene)-b-styrene) (SEBS) elastomer via covalent immobilization of nonionic sugar-based Gemini surfactants.

    Science.gov (United States)

    Xin, Zhirong; Du, Binbin; Yan, Shunjie; Du, Shanshan; Ding, Jiaotong; Yang, Zongfeng; Ren, Wanzhong

    2014-07-01

    Gemini surfactants (GS) with sugar-containing head-groups and different alkyl chains were successfully prepared. Poly(styrene-b-(ethylene-co-butylene)-b-styrene) (SEBS) elastomer was grafted with glycidyl methacrylate (GMA) by means of UV-induced graft polymerization, and then the pGMA-grafted film was chemically immobilized with the GS. The surface graft polymerization was confirmed by ATR-FTIR and XPS. The wettability and hemocompatibility of the modified surface were characterized by means of water contact angle, protein adsorption, and platelet adhesion assays. The results showed that amphiphilic surfactant-containing polymer surfaces presented protein-resistant behavior and anti-platelet adhesion after functionalization with GS, GS1 and GS2. Besides, the hemocompatibility of the modified surface deteriorated as the length of hydrophobic chain of GS increased. PMID:24854325

  12. Surface modification of poly(styrene-b-(ethylene-co-butylene)-b-styrene) elastomer via UV-induced graft polymerization of N-vinyl pyrrolidone.

    Science.gov (United States)

    Luan, Shifang; Zhao, Jie; Yang, Huawei; Shi, Hengchong; Jin, Jing; Li, Xiaomeng; Liu, Jingchuan; Wang, Jianwei; Yin, Jinghua; Stagnaro, Paola

    2012-05-01

    Poly(N-vinyl pyrrolidone) (PNVP) was covalently grafted onto the surface of biomedical poly(styrene-b-(ethylene-co-butylene)-b-styrene) (SEBS) elastomer via a technique of UV-induced graft polymerization combined with plasma pre-treatment. The surface graft polymerization of N-vinyl pyrrolidone (NVP) was confirmed by ATR-FTIR and XPS. Effect of the parameters of graft polymerization, i.e., the initiator concentration, the UV irradiation time and the monomer concentration on the grafting density was investigated. The morphology and the wettability of the PNVP-modified surfaces were characterized by AFM and DSA, respectively. Protein adsorption and platelet adhesion were obviously suppressed after PNVP was grafted onto the SEBS substrates. PMID:22264686

  13. Novel membrane-based biotechnological alternative process for succinic acid production and chemical synthesis of bio-based poly (butylene succinate).

    Science.gov (United States)

    Wang, Caixia; Ming, Wei; Yan, Daojiang; Zhang, Congcong; Yang, Maohua; Liu, Yilan; Zhang, Yu; Guo, Baohua; Wan, Yinhua; Xing, Jianmin

    2014-03-01

    Succinic acid was produced in a novel membrane-based fermentation and separation integrated system. With this integrated system, product inhibition was alleviated by removing acids and replenishing fresh broth. High cell density maintain for a longer time from 75 to 130h and succinic acid concentration increased from 53 to 73g/L. In the developed separation process, succinic acid was crystallized at a recovery of 85-90%. The purity of the obtained succinic acid crystals reached 99.4% as found by HPLC and (1)H NMR analysis. A crystallization experiment indicated that among by-products glucose had a negative effect on succinic acid crystallization. Poly (butylene succinate) (PBS) was synthesized using the purified succinic acid and (1)H NMR analysis confirmed that the composition of the synthesized PBS is in agreement with that from petro-based succinic acid. PMID:24472699

  14. Effects of thermal history in the ring opening polymerization of CBT and its mixtures with montmorillonite on the crystallization of the resulting poly(butylene terephthalate)

    Energy Technology Data Exchange (ETDEWEB)

    Lanciano, Giuseppina [Department of Innovation Engineering, University of Salento, Via per Arnesano, 73100 Lecce (Italy); Greco, Antonio, E-mail: antonio.greco@unile.it [Department of Innovation Engineering, University of Salento, Via per Arnesano, 73100 Lecce (Italy); Maffezzoli, Alfonso [Department of Innovation Engineering, University of Salento, Via per Arnesano, 73100 Lecce (Italy); Mascia, Leno [Department of Materials, Loughborough University, Loughborough, LE 11 3TU (United Kingdom)

    2009-09-10

    Differential scanning calorimetry was used to study the thermal characteristics and morphological structure of species produced during the ring opening polymerization of cyclic butylene terephthalate (CBT). Thermal programs consisting of a first ramp heating scan and an isothermal step, followed by cooling and a second ramp heating step, were used to study the effects of thermal history, catalyst (butyl chlorotin dihydroxide) at concentrations between 0.1 and 1.3% (w/w), and the presence of a layered silicate nanofiller (montmorillonite at 4.0%, w/w) on the structure of the resulting polymer (poly(butylene terephthalate), pCBT). Wide angle X-ray diffraction was used to monitor the degree of exfoliation of the nanocomposites. It was found that pCBT is formed in the amorphous state, and crystallizes during the heating step or during the isothermal step at temperatures lower than the equilibrium melting temperature of the polymer (T{sub m}{sup 0}). When premixed with the nanofiller, irrespective of whether this was previously intercalated with a tallow surfactant or used in its pristine form, polymerization took place at higher temperatures and most of the crystallization was found to occur during the cooling stage. In those cases where crystallization took place during either the first heating scan, or during a prolonged isothermal step below the T{sub m}{sup 0} of the polymer, the resulting crystals were found to have a higher lamellar thickness, as compared with the same polymer crystallized from the melt during the cooling step from temperatures above the polymer T{sub m}{sup 0}.

  15. Poly(butylene terephthalate)/montmorillonite nanocomposites: Effect of montmorillonite on the morphology, crystalline structure, isothermal crystallization kinetics and mechanical properties

    Energy Technology Data Exchange (ETDEWEB)

    Kalkar, Arun K., E-mail: drarunkalkar@gmail.com; Deshpande, Vineeta D.; Vatsaraj, Bhakti S.

    2013-09-20

    Graphical abstract: - Highlights: • Effect of amount of clay content, its dispersion on crystalline structure of PBT. • Regime break temperature shifts to lower temperature for PCN4 up to 197 °C. • Tensile modulus enhanced up to 95% for PCN3 compared to PBT. - Abstract: Nanocomposites (PCNs), based on poly(butylene terephthalte) (PBT) and organoclay (Cloisite-15A) MMT were prepared by melt intercalation compounding process. The nanoscale dispersion and the microcrystal structure studied qualitatively using; X-ray diffraction (XRD) and electron microscopy (SEM, TEM and AFM). The XRD results indicated that the crystal size is highly dependent on the crystallization temperature. The isothermal crystallization kinetics of PBT in PCNs analysis indicated that the overall crystallization of PBT involved heterogeneous nucleated three-dimensional spherical primary crystallization growth process. The crystallization rate, however, is dependent on the PCN-composition, crystallization temperature and the dispersion state of clay in PCNs. Further analysis, based on Hoffman-Lauritzen theory revealed that the neat PBT and PBT in PCNs crystallization follow regime-II kinetics for temperature 195 °C–205 °C and enters the regime-III kinetics in lower T{sub c} range, 185 °C–195 °C. The improvement in mechanical properties is highly dependent on the level of clay exfoliation in PBT matrix.

  16. Investigation on Polylactide (PLA/Poly(butylene adipate-co-terephthalate (PBAT/Bark Flour of Plane Tree (PF Eco-Composites

    Directory of Open Access Journals (Sweden)

    Qiang Dou

    2016-05-01

    Full Text Available Polylactide (PLA/poly(butylene adipate-co-terephthalate (PBAT/bark flour of plane tree (PF eco-composites were prepared via melt blending. The morphologies, mechanical properties, crystal structures and melting and crystallization behaviors of the eco-composites were investigated by means of scanning electron microscopy (SEM, mechanical tests, polarized light microscopy (PLM, wide angle X-ray diffraction (WAXD and differential scanning calorimetry (DSC, respectively. It is shown that the interfacial adhesion between PLA matrix and PF is weak and the mechanical properties of PLA/PF eco-composites are poor. The titanate treatment improves the adhesion between the matrix and the filler and enhances the stiffness of the eco-composites. The toughness is improved by PBAT and ductile fractured surfaces can be found. The spherulitic size of PLA is decreased by the addition of PF. The α crystalline form of PLA remains in the composites. Compared with PF, T-PF (PF treated by a titanate coupling agent and PBAT have negative effects on the crystallization of PLA.

  17. Active biodegradable films produced with blends of rice flour and poly(butylene adipate co-terephthalate): effect of potassium sorbate on film characteristics.

    Science.gov (United States)

    Sousa, G M; Soares Júnior, M S; Yamashita, F

    2013-08-01

    The objective of work was to produce and characterize biodegradable films from rice flour, poly(butylene adipate co-terephthalate) (PBAT), glycerol and potassium sorbate, for application as active packaging for fresh lasagna pasta. The films were evaluated with respect to their optical, water vapor barrier, mechanical and microstructural properties. The mechanical properties and microstructure were evaluated after use as packaging material for fresh pasta for 45 days at 7°C. The blends of rice flour, PBAT, glycerol and potassium sorbate showed good processability and allowed for the pilot scale production of films by blow extrusion process. The addition of 1 to 5% potassium sorbate as plasticizer agent of films in place of glycerol did not alter the film mechanical properties and a sorbate concentration greater or equal than 3% reduced the opacity, although increasing the water vapor permeability. The films could be used as active packaging for fresh food pasta, since they remained integral and easy to handle after application. The rice flour was shown to be an excellent material for the formulation of biodegradable films, since it is a low-cost raw material from a renewable source. The addition of potassium sorbate did not affect the extrusion process, and could be used in the production of packaging for use with foods. PMID:23706195

  18. Effect of Chain-Extenders on the Properties and Hydrolytic Degradation Behavior of the Poly(lactide/ Poly(butylene adipate-co-terephthalate Blends

    Directory of Open Access Journals (Sweden)

    Mingqing Chen

    2013-10-01

    Full Text Available Biodegradable poly(lactide/poly(butylene adipate-co-terephthalate (PLA/PBAT blends were prepared by reactive blending in the presence of chain-extenders. Two chain-extenders with multi-epoxy groups were studied. The effect of chain-extenders on the morphology, mechanical properties, thermal behavior, and hydrolytic degradation of the blends was investigated. The compatibility between the PLA and PBAT was significantly improved by in situ formation of PLA-co-PBAT copolymers in the presence of the chain-extenders, results in an enhanced ductility of the blends, e.g., the elongation at break was increased to 500% without any decrease in the tensile strength. The differential scanning calorimeter (DSC results reveal that cold crystallization of PLA was enhanced due to heterogeneous nucleation effect of the in situ compatibilized PBAT domains. As known before, PLA is sensitive to hydrolysis and in the presence of PBAT and the chain-extenders, the hydrolytic degradation of the blend was evident. A three-stage hydrolysis mechanism for the system is proposed based on a study of weight loss and molecular weight reduction of the samples and the pH variation of the degradation medium.

  19. Heat Treatment Effects on the Mechanical Properties and Morphologies of Poly (Lactic Acid/Poly (Butylene Adipate-co-terephthalate Blends

    Directory of Open Access Journals (Sweden)

    Hsien-Tang Chiu

    2013-01-01

    Full Text Available In this study the relationships between mechanicals properties and morphology of the poly (lactic acid (PLA/poly (butylene adipate-co-terephthalate (PBAT blends with or without heat treatment were investigated. The differential scanning calorimetry (DSC analysis showed that blends have a two-phase structure indicating that they are immiscible. On the other hand, the PLA/PBAT (30/70 blend achieved the best tensile and impact strength because of its sea-island morphology, except for high PBAT content. The PLA/PBAT (70/30 and PLA/PBAT (50/50 blends showed irregular and directive-layer morphologies, in scanning electron microscopy (SEM analysis, producing a break cross-section with various fiber shapes. Both blends showed lower tensile strength and impact strength than the PLA/PBAT (30/70. After heat treatment, the PLA/PBAT blends showed high modulus of tensile and HDT because of a high degree of crystallization. The high degree of crystallization in the blends, which originated in the heat treatment, reduced their impact strength and elongation. However, the effect of high degree of crystallization on the PLA/PBAT (30/70 blend was small because of its sea-island morphology.

  20. Cross-Linked Quaternized Poly(styrene-b-(ethylene-co-butylene)-b-styrene) for Anion Exchange Membrane: Synthesis, Characterization and Properties.

    Science.gov (United States)

    Dai, Pei; Mo, Zhao-Hua; Xu, Ri-Wei; Zhang, Shu; Wu, Yi-Xian

    2016-08-10

    Poly(styrene-b-(ethylene-co-butylene)-b-styrene) triblock copolymer (SEBS) was selected for functionalization and cross-linking reaction to prepare the anion exchange membrane. The cross-linked quaternized SEBS (QSEBS-Cn) membranes were synthesized by simultaneous of quaternization and cross-linking of chloromethylated SEBS with α,ω-difunctional tertiary amines. The spacer groups of (-CH2-)n in diamines did affect the functionalization, micromorphology and properties of the resulting QSEBS-Cn membranes. The ionic conductivity of QSEBS-Cn membranes greatly increased and methanol resistance slightly decreased with increasing the length of spacer groups in the cross-linked structures from -(CH2)- to -(CH2)6-. Compared to the un-cross-linked QSEBS, the QSEBS-Cn membranes behaved much higher mechanical property, service temperature, chemical stability and thermal stability. Moreover, the hybrid composite membrane of QSEBS-C6 with 0.5% of graphene oxide could also be in situ prepared. This hybrid membrane had both relatively high ionic conductivity of 2.0 × 10(-2) S·cm(-1) and high selectivity of 7.6 × 10(4) S·s·cm(-3) at 60 °C due to its low methanol permeability. PMID:27459593

  1. Influence of melt processing induced orientation on the morphology and mechanical properties of poly(styrene-b-ethylene/butylene-b-styrene) block copolymers and their composites with graphite

    International Nuclear Information System (INIS)

    Highlights: • Orientation was induced during processing of SEBS, SEBS-MA and their composites. • Static and dynamic mechanical tests in perpendicular directions were performed. • 400–1600% difference in Young’s or storage modulus in function of orientation. • Micro/nanoscale morphology and orientation investigated by POM, SEM and AFM. • A method to improve the mechanical behavior by morphology control was proposed. - Abstract: The effect of orientation induced during the manufacturing process on the self-assembled morphology and mechanical properties of poly(styrene-b-ethylene/butylene-b-styrene) block copolymer (SEBS), maleated SEBS (SEBS-MA) and their composites with graphite was examined in this paper. The roll milling process induced higher stiffness along the rolling direction, emphasized by the increase of Young’s modulus with 645% in this direction relative to the perpendicular one and the increase of storage modulus at room temperature with one order of magnitude. The addition of graphite particles diminished the anisotropy of static and dynamic mechanical properties but contributed to the increase of the total energy absorbed till break. The different self-assembled morphologies and degree of order observed by polarized optical microscopy (POM), scanning electron microscopy (SEM) and atomic force microscopy (AFM) in SEBS and SEBS-MA explained some of the differences in their static and dynamic mechanical behavior. For the first time the anisotropy was emphasized by the different glass transition values obtained on the two stretching directions

  2. Effect of nanoclay loading on the thermal and mechanical properties of biodegradable polylactide/poly[(butylene succinate)-co-adipate] blend composites.

    Science.gov (United States)

    Ojijo, Vincent; Sinha Ray, Suprakas; Sadiku, Rotimi

    2012-05-01

    Polylactide/poly[(butylene succinate)-co-adipate] (PLA/PBSA)-organoclay composites were prepared via melt compounding in a batch mixer. The weight ratio of PLA to PBSA was kept at 70:30, while the weight fraction of the organoclay was varied from 0 to 9%. Small angle X-ray scattering patterns showed slightly better dispersion in PBSA than PLA, and there was a tendency of the silicate layers to delaminate in PBSA at low clay content. Thermal analysis revealed that crystallinity was dependent on the clay content as well its localization within the composite. On the other hand, thermal stability marginally improved for composites with 2 wt %. Tensile properties showed dependence on clay content and localization. Composite with 2 wt % clay content showed slight improvement in elongation at break. Overall, the optimum property was found for a composite with 2 wt % of the organoclay. This paper therefore has demonstrated the significance of the clay content and localization on the properties of the PLA/PBSA blends.

  3. Role of specific interfacial area in controlling properties of immiscible blends of biodegradable polylactide and poly[(butylene succinate)-co-adipate].

    Science.gov (United States)

    Ojijo, Vincent; Sinha Ray, Suprakas; Sadiku, Rotimi

    2012-12-01

    Binary blends of two biodegradable polymers: polylactide (PLA), which has high modulus and strength but is brittle, and poly[(butylene succinate)-co-adipate] (PBSA), which is flexible and tough, were prepared through batch melt mixing. The PLA/PBSA compositions were 100/0, 90/10, 70/30, 60/40, 50/50, 40/60, 30/70, 10/90, and 0/100. Fourier-transform infrared measurements revealed the absence of any chemical interaction between the two polymers, resulting in a phase-separated morphology as shown by scanning electron microscopy (SEM). SEM micrographs showed that PLA-rich blends had smaller droplet sizes when compared to the PBSA-rich blends, which got smaller with the reduction in PBSA content due to the differences in their melt viscosities. The interfacial area of PBSA droplets per unit volume of the blend reached a maximum in the 70PLA/30PBSA blend. Thermal stability and mechanical properties were not only affected by the composition of the blend, but also by the interfacial area between the two polymers. Through differential scanning calorimetry, it was shown that molten PBSA enhanced crystallization of PLA while the stiff PLA hindered cold crystallization of PBSA. Optimal synergies of properties between the two polymers were found in the 70PLA/30PBSA blend because of the maximum specific interfacial area of the PBSA droplets.

  4. The Influence of Green Surface Modification of Oil Palm Mesocarp Fiber by Superheated Steam on the Mechanical Properties and Dimensional Stability of Oil Palm Mesocarp Fiber/Poly(butylene succinate) Biocomposite

    OpenAIRE

    Yoon Yee Then; Nor Azowa Ibrahim; Norhazlin Zainuddin; Hidayah Ariffin; Wan Md Zin Wan Yunus; Buong Woei Chieng

    2014-01-01

    In this paper, superheated steam (SHS) was used as cost effective and green processing technique to modify oil palm mesocarp fiber (OPMF) for biocomposite applications. The purpose of this modification was to promote the adhesion between fiber and thermoplastic. The modification was carried out in a SHS oven at various temperature (200–230 °C) and time (30–120 min) under normal atmospheric pressure. The biocomposites from SHS-treated OPMFs and poly(butylene succinate) (PBS) at a weight ratio ...

  5. Enhancement of Mechanical and Thermal Properties of Oil Palm Empty Fruit Bunch Fiber Poly(butylene adipate-co-terephtalate Biocomposites by Matrix Esterification Using Succinic Anhydride

    Directory of Open Access Journals (Sweden)

    Samira Siyamak

    2012-02-01

    Full Text Available In this work, the oil palm empty fruit bunch (EFB fiber was used as a source of lignocellulosic filler to fabricate a novel type of cost effective biodegradable composite, based on the aliphatic aromatic co-polyester poly(butylene adipate-co-terephtalate PBAT (EcoflexTM, as a fully biodegradable thermoplastic polymer matrix. The aim of this research was to improve the new biocomposites’ performance by chemical modification using succinic anhydride (SAH as a coupling agent in the presence and absence of dicumyl peroxide (DCP and benzoyl peroxide (BPO as initiators. For the composite preparation, several blends were prepared with varying ratios of filler and matrix using the melt blending technique. The composites were prepared at various fiber contents of 10, 20, 30, 40 and 50 (wt % and characterized. The effects of fiber loading and coupling agent loading on the thermal properties of biodegradable polymer composites were evaluated using thermal gravimetric analysis (TGA. Scanning Electron Microscopy (SEM was used for morphological studies. The chemical structure of the new biocomposites was also analyzed using the Fourier Transform Infrared (FTIR spectroscopy technique. The PBAT biocomposite reinforced with 40 (wt % of EFB fiber showed the best mechanical properties compared to the other PBAT/EFB fiber biocomposites. Biocomposite treatment with 4 (wt % succinic anhydride (SAH and 1 (wt % dicumyl peroxide (DCP improved both tensile and flexural strength as well as tensile and flexural modulus. The FTIR analyses proved the mechanical test results by presenting the evidence of successful esterification using SAH/DCP in the biocomposites’ spectra. The SEM micrograph of the tensile fractured surfaces showed the improvement of fiber-matrix adhesion after using SAH. The TGA results showed that chemical modification using SAH/DCP improved the thermal stability of the PBAT/EFB biocomposite.

  6. Effect of fiber esterification on fundamental properties of oil palm empty fruit bunch fiber/poly(butylene adipate-co-terephthalate) biocomposites.

    Science.gov (United States)

    Siyamak, Samira; Ibrahim, Nor Azowa; Abdolmohammadi, Sanaz; Yunus, Wan Md Zin Wan; Rahman, Mohamad Zaki Ab

    2012-01-01

    A new class of biocomposites based on oil palm empty fruit bunch fiber and poly(butylene adipate-co-terephthalate) (PBAT), which is a biodegradable aliphatic aromatic co-polyester, were prepared using melt blending technique. The composites were prepared at various fiber contents of 10, 20, 30, 40 and 50 wt% and characterized. Chemical treatment of oil palm empty fruit bunch (EFB) fiber was successfully done by grafting succinic anhydride (SAH) onto the EFB fiber surface, and the modified fibers were obtained in two levels of grafting (low and high weight percentage gain, WPG) after 5 and 6 h of grafting. The FTIR characterization showed evidence of successful fiber esterification. The results showed that 40 wt% of fiber loading improved the tensile properties of the biocomposite. The effects of EFB fiber chemical treatments and various organic initiators content on mechanical and thermal properties and water absorption of PBAT/EFB 60/40 wt% biocomposites were also examined. The SAH-g-EFB fiber at low WPG in presence of 1 wt% of dicumyl peroxide (DCP) initiator was found to significantly enhance the tensile and flexural properties as well as water resistance of biocomposite (up to 24%) compared with those of untreated fiber reinforced composites. The thermal behavior of the composites was evaluated from thermogravimetric analysis (TGA)/differential thermogravimetric (DTG) thermograms. It was observed that, the chemical treatment has marginally improved the biocomposites' thermal stability in presence of 1 wt% of dicumyl peroxide at the low WPG level of grafting. The improved fiber-matrix surface enhancement in the chemically treated biocomposite was confirmed by SEM analysis of the tensile fractured specimens. PMID:22408394

  7. Osteoconductive bio-based meshes based on Poly(hydroxybutyrate-co-hydroxyvalerate) and poly(butylene adipate-co-terephthalate) blends

    Energy Technology Data Exchange (ETDEWEB)

    Nar, Mangesh; Staufenberg, Gerrit; Yang, Bing [Department of Material Science and Engineering, University of North Texas, 1155 Union Circle #305310, Denton, TX 76203-5017 (United States); Robertson, Lesli [Department of Fibers, College of Visual Arts and Design, 1155 Union Circle #305100, Denton, TX 76203-5017 (United States); Patel, Rinkesh H. [Department of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A and M University Baylor College of Dentistry, Dallas, TX 75246 (United States); Varanasi, Venu G., E-mail: vvaranasi@bcd.tamhsc.edu [Department of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A and M University Baylor College of Dentistry, Dallas, TX 75246 (United States); D' Souza, Nandika Anne, E-mail: nandika.dsouza@unt.edu [Department of Material Science and Engineering, University of North Texas, 1155 Union Circle #305310, Denton, TX 76203-5017 (United States); Department of Mechanical and Energy Engineering, University of North Texas, 1155 Union Circle # 311098, Denton, TX 76203-5017 (United States)

    2014-05-01

    Poly(butylene adipate-co-terephthalate) (PBAT) and Poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV) are biopolymers that have the potential to be used in applications of bone healing. In this study, it is hypothesized that the polymer blend has the combined strength and osteoconductivity to support osteoblast collagen formation. PBAT (PBAT 100), and a blend with 20% PHBV (PBAT 80) were extruded in the form of fibers and then knitted in the form of mesh. These were tested in the warp as well as weft direction for the tensile properties; these showed that the weft direction had higher performance than the warp. The individual fibers were kept in phosphate buffered saline (PBS) over the period of 8 weeks and were tested for the storage and loss modulus using a dynamic mechanical analyser (DMA). The results indicated that mechanical relaxation strength showed a decrease and then an increase. In vitro osteoconductivity studies were done by using differentiating osteoblasts (MC3T3-E1 subclone 4 cells). Environmental Scanning Electron Microscopy (ESEM) showed that pre-soaking the samples in α-MEM for two weeks resulted in cell attachment and growth. X-ray diffraction (XRD) was used to determine the change in structure of polymers due to in vitro degradation for two weeks. Raman spectroscopy showed that all scaffolds supported the formation of a collagenous network over the scaffold surfaces. For a combination of knittable manufacturing, mechanical performance and osteoconductivity, blends offer an effective route. - Highlights: • PBAT and PHBV blend can be knitted to form mesh with good mechanical properties. • PBAT and PHBV blend do not show significant weight loss over a period of 8 weeks in PBS. • Osteoblast cell culture was done on these samples. • They support extracellular matrix and growth and hence are osteoconductive.

  8. Super-Robust Polylactide Barrier Films by Building Densely Oriented Lamellae Incorporated with Ductile in Situ Nanofibrils of Poly(butylene adipate-co-terephthalate).

    Science.gov (United States)

    Zhou, Sheng-Yang; Huang, Hua-Dong; Ji, Xu; Yan, Ding-Xiang; Zhong, Gan-Ji; Hsiao, Benjamin S; Li, Zhong-Ming

    2016-03-01

    Remarkable combination of excellent gas barrier performance, high strength, and toughness was realized in polylactide (PLA) composite films by constructing the supernetworks of oriented and pyknotic crystals with the assistance of ductile in situ nanofibrils of poly(butylene adipate-co-terephthalate) (PBAT). On the basis that the permeation of gas molecules through polymer materials with anisotropic structure would be more frustrated, we believe that oriented crystalline textures cooperating with inerratic amorphism can be favorable for the enhancement of gas barrier property. By taking full advantage of intensively elongational flow field, the dispersed phase of PBAT in situ forms into nanofibrils, and simultaneously sufficient row-nuclei for PLA are induced. After appropriate thermal treatment with the acceleration effect of PBAT on PLA crystallization, oriented lamellae of PLA tend to be more perfect in a preferential direction and constitute into a kind of network interconnecting with each other. At the same time, the molecular chains between lamellae tend to be more extended. This unique structure manifests superior ability in ameliorating the performance of PLA film. The oxygen permeability coefficient can be achieved as low as 2 × 10(-15) cm(3) cm cm(-2) s(-1) Pa(-1), combining with the high strength, modulus, and ductility (104.5 MPa, 3484 MPa, and 110.6%, respectively). The methodology proposed in this work presents an industrially scalable processing method to fabricate super-robust PLA barrier films. It would indeed push the usability of biopolymers forward, and certainly prompt wider application of biodegradable polymers in the fields of environmental protection such as food packaging, medical packaging, and biodegradable mulch. PMID:26959220

  9. Poly(trimethylene terephthalate)/Poly(butylenes succinate) blend: Phase behavior and mechanical property control using its transesterification system as the compatibilizer

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Jianxiang [School of Chemistry and Chemical Engineering, Yangzhou University, Jiangsu 225002 (China); Provincial Key Laboratory of Environmental Material and Engineering, Jiangsu 225002 (China); Wu, Defeng, E-mail: dfwu@yzu.edu.cn [School of Chemistry and Chemical Engineering, Yangzhou University, Jiangsu 225002 (China); Provincial Key Laboratory of Environmental Material and Engineering, Jiangsu 225002 (China)

    2014-12-15

    Poly(trimethylene terephthalate)/poly(butylenes succinate) (PTT/PBS) blends and their ester-exchanged system were prepared by melt mixing for the phase behavior and the viscoelasticity studies. A typical two-phase structure can be seen on the blends because two polymers are immiscible thermodynamically. The phase inversion behavior of the blends can be well determined by the blending ratio dependence of their dynamic rheological responses, which can also be predicted by the viscous Utracki model based on the viscosity ratio. However, the dynamic viscoelastic responses of the blends cannot be well described by the emulsion model because two polymers are highly asymmetric in their viscoelasticity. Besides, transesterification is an effective approach of reducing interfacial tension and improving final phase morphology of the blends, which can be evaluated qualitatively from viscoelastic response alterations after ester exchange reaction. The mechanical properties of PTT/PBS blends were also studied. The results reveal that the ester-exchanged blends show mechanical strengths even lower than the pristine ones because of bulk degradation accompanied with transesterification, despite their improved phase structure. However, they can be used as the good compatibilizer to improve phase adhesion of the pristine blends, enhancing strengths of the PTT based blends or toughness of the PBS based blends evidently. - Highlights: • Phase inversion of the blends can be determined by their rheological responses. • Improved phase morphology can be evaluated from viscoelasticity alterations. • The ester-exchanged system is suitable to be used as the compatibilizer. • Mechanical properties can be controlled by introducing ester-exchanged system.

  10. Novel ether-linkages containing aliphatic copolyesters of poly(butylene 1,4-cyclohexanedicarboxylate) as promising candidates for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Gigli, Matteo [Department of Civil, Chemical, Environmental and Materials Engineering (DICAM), University of Bologna, Via Terracini 28, 40131 Bologna (Italy); Lotti, Nadia, E-mail: nadia.lotti@unibo.it [Department of Civil, Chemical, Environmental and Materials Engineering (DICAM), University of Bologna, Via Terracini 28, 40131 Bologna (Italy); Vercellino, Marco [Department of Molecular Medicine, UdR of INSTM, Viale Taramelli 3/B, University of Pavia, Pavia (Italy); Visai, Livia [Department of Molecular Medicine, UdR of INSTM, Viale Taramelli 3/B, University of Pavia, Pavia (Italy); Department of Occupational Medicine, Ergonomics and Disability, Salvatore Maugeri Foundation, IRCCS, Laboratory of Nanotechnology, Via S. Maugeri 8, 27100 Pavia (Italy); Munari, Andrea [Department of Civil, Chemical, Environmental and Materials Engineering (DICAM), University of Bologna, Via Terracini 28, 40131 Bologna (Italy)

    2014-01-01

    A new class of biodegradable and biocompatible poly(butylene 1,4-cyclohexanedicarboxylate) based random copolymers are proposed for biomedical applications. The introduction of ether–oxygen containing BDG sequences along the PBCE macromolecular chain is expected to remarkably improve chain flexibility and surface hydrophilicity due to the presence of highly electronegative oxygen atoms. P(BCExBDGy) copolymers were synthesized by polycondensation. The homopolymer PBCE and three copolymers, namely (P(BCE70BDG30), P(BCE55BDG45) and P(BCE40BDG60)) were characterized from the molecular, thermal, structural and mechanical point of view. Hydrolytic degradation studies in the presence and absence of hog-pancreas lipase were performed under physiological conditions. To evaluate the diffusion profile of small molecules through the polymer matrix, the release behaviour of fluorescein isothiocyanate (FITC) was investigated. For biocompatibility studies, cell adhesion and proliferation of murine fibroblast (L929) and endocrine pancreatic (INS-1) cells were performed on each polymeric film. Results showed that solid-state properties can be tailored by simply varying copolymers' composition. Crystallinity degree and hydrophobicity significantly decreased with the increase of BDG co-unit mol%. Moreover, mechanical properties and biodegradability of PBCE, both depending on crystallinity degree, were remarkably improved: P(BCE40BDG60) showed an elastomeric behaviour with ε{sub b} over 600% and, as regard to biodegradability, after 98 days it lost over 60% of its initial weight if incubated in the presence of the pancreatic lipase. Lastly, the newly developed biomaterials resulted not cytotoxic with both types of cells and could be properly tailored for biomedical applications varying the content of BDG co-unit mol%. - Highlights: • Ether–oxygen atoms along PBCE chain as winning strategy to improve its properties • Adjustable solid-state properties of copolymers simply

  11. Novel electrospun nanofibrous matrices prepared from poly(lactic acid)/poly(butylene adipate) blends for controlled release formulations of an anti-rheumatoid agent.

    Science.gov (United States)

    Siafaka, Panoraia I; Barmbalexis, Panagiotis; Bikiaris, Dimitrios N

    2016-06-10

    In the present work, a series of novel formulations consisting of poly(lactic acid)/poly(butylene adipate) (PLA/PBAd) electrospun blends was examined as controlled release matrices for Leflunomide's active metabolite, Teriflunomide (TFL). The mixtures were prepared using different ratios of PLA and PBAd in order to produce nanofibrous matrices with different characteristics. Miscibility studies of the blended polymeric fibers were performed through differential scanning calorimetry (DSC) and X-ray diffractometry (XRD). Hydrolytic degradation in the prepared fibers was evaluated at 37°C using a phosphate buffered saline solution. Different concentrations of (TFL) (5, 10, 15wt.%) were incorporated into nanofibers for examining the drug release behavior in simulated body fluids (SBF), at 37°C. The drug-loaded nanofibrous formulations were further characterized by Fourier Transform Infrared Spectroscopy (FTIR) spectroscopy, DSC and XRD. Gel permeation chromatography (GPC) analysis was used to evaluate the mechanism of TFL release. Artificial neural networks (ANN) and multi-linear-regression (MLR) models were used to evaluate the effect of % content of PBAd (X1) and TFL (X2) on an initial burst effect and a dissolution behavior. It was found that PLA/PBAd nanofibers have different diameters depending on the ratio of used polyesters and added drug. TFL was incorporated in an amorphous form inside the polymeric nanofibers. In vitro release studies reveal that a drug release behavior is correlated with the size of the nanofibers, drug loading and matrix degradation after a specific time. ANN dissolution modeling showed increased correlation efficacy compared to MLR. PMID:27039136

  12. Influence of low contents of superhydrophilic MWCNT on the properties and cell viability of electrospun poly (butylene adipate-co-terephthalate) fibers.

    Science.gov (United States)

    Rodrigues, Bruno V M; Silva, Aline S; Melo, Gabriela F S; Vasconscellos, Luana M R; Marciano, Fernanda R; Lobo, Anderson O

    2016-02-01

    The use of poly (butylene adipate-co-terephthalate) (PBAT) in tissue engineering, more specifically in bone regeneration, has been underexplored to date due to its poor mechanical resistance. In order to overcome this drawback, this investigation presents an approach into the preparation of electrospun nanocomposite fibers from PBAT and low contents of superhydrophilic multi-walled carbon nanotubes (sMWCNT) (0.1-0.5wt.%) as reinforcing agent. We employed a wide range of characterization techniques to evaluate the properties of the resulting electrospun nanocomposites, including Field Emission Scanning Electronic Microscopy (FE-SEM), Transmission Electronic Microscopy (TEM), tensile tests, contact angle measurements (CA) and biological assays. FE-SEM micrographs showed that while the addition of sMWCNT increased the presence of beads on the electrospun fibers' surfaces, the increase of the neat charge density due to their presence reduced the fibers' average diameter. The tensile test results pointed that sMWCNT acted as reinforcement in the PBAT electrospun matrix, enhancing its tensile strength (from 1.3 to 3.6MPa with addition of 0.5wt.% of sMWCNT) and leading to stiffer materials (lower elongation at break). An evaluation using MG63 cells revealed cell attachment into the biomaterials and that all samples were viable for biomedical applications, once no cytotoxic effect was observed. MG-63 cells osteogenic differentiation, measured by ALP activity, showed that mineralized nodules formation was increased in PBAT/0.5%CNTs when compared to control group (cells). This investigation demonstrated a feasible novel approach for producing electrospun nanocomposites from PBAT and sMWCNT with enhanced mechanical properties and adequate cell viability levels, which allows for a wide range of biomedical applications for these materials. PMID:26652433

  13. Effect of Fiber Esterification on Fundamental Properties of Oil Palm Empty Fruit Bunch Fiber/Poly(butylene adipate-co-terephthalate Biocomposites

    Directory of Open Access Journals (Sweden)

    Mohamad Zaki AB Rahman

    2012-01-01

    Full Text Available A new class of biocomposites based on oil palm empty fruit bunch fiber and poly(butylene adipate-co-terephthalate (PBAT, which is a biodegradable aliphatic aromatic co-polyester, were prepared using melt blending technique. The composites were prepared at various fiber contents of 10, 20, 30, 40 and 50 wt% and characterized. Chemical treatment of oil palm empty fruit bunch (EFB fiber was successfully done by grafting succinic anhydride (SAH onto the EFB fiber surface, and the modified fibers were obtained in two levels of grafting (low and high weight percentage gain, WPG after 5 and 6 h of grafting. The FTIR characterization showed evidence of successful fiber esterification. The results showed that 40 wt% of fiber loading improved the tensile properties of the biocomposite. The effects of EFB fiber chemical treatments and various organic initiators content on mechanical and thermal properties and water absorption of PBAT/EFB 60/40 wt% biocomposites were also examined. The SAH-g-EFB fiber at low WPG in presence of 1 wt% of dicumyl peroxide (DCP initiator was found to significantly enhance the tensile and flexural properties as well as water resistance of biocomposite (up to 24% compared with those of untreated fiber reinforced composites. The thermal behavior of the composites was evaluated from thermogravimetric analysis (TGA/differential thermogravimetric (DTG thermograms. It was observed that, the chemical treatment has marginally improved the biocomposites’ thermal stability in presence of 1 wt% of dicumyl peroxide at the low WPG level of grafting. The improved fiber-matrix surface enhancement in the chemically treated biocomposite was confirmed by SEM analysis of the tensile fractured specimens.

  14. Enhancement of mechanical and thermal properties of oil palm empty fruit bunch fiber poly(butylene adipate-co-terephtalate) biocomposites by matrix esterification using succinic anhydride.

    Science.gov (United States)

    Siyamak, Samira; Ibrahim, Nor Azowa; Abdolmohammadi, Sanaz; Yunus, Wan Md Zin Bin Wan; Rahman, Mohamad Zaki Ab

    2012-01-01

    In this work, the oil palm empty fruit bunch (EFB) fiber was used as a source of lignocellulosic filler to fabricate a novel type of cost effective biodegradable composite, based on the aliphatic aromatic co-polyester poly(butylene adipate-co-terephtalate) PBAT (Ecoflex™), as a fully biodegradable thermoplastic polymer matrix. The aim of this research was to improve the new biocomposites' performance by chemical modification using succinic anhydride (SAH) as a coupling agent in the presence and absence of dicumyl peroxide (DCP) and benzoyl peroxide (BPO) as initiators. For the composite preparation, several blends were prepared with varying ratios of filler and matrix using the melt blending technique. The composites were prepared at various fiber contents of 10, 20, 30, 40 and 50 (wt %) and characterized. The effects of fiber loading and coupling agent loading on the thermal properties of biodegradable polymer composites were evaluated using thermal gravimetric analysis (TGA). Scanning Electron Microscopy (SEM) was used for morphological studies. The chemical structure of the new biocomposites was also analyzed using the Fourier Transform Infrared (FTIR) spectroscopy technique. The PBAT biocomposite reinforced with 40 (wt %) of EFB fiber showed the best mechanical properties compared to the other PBAT/EFB fiber biocomposites. Biocomposite treatment with 4 (wt %) succinic anhydride (SAH) and 1 (wt %) dicumyl peroxide (DCP) improved both tensile and flexural strength as well as tensile and flexural modulus. The FTIR analyses proved the mechanical test results by presenting the evidence of successful esterification using SAH/DCP in the biocomposites' spectra. The SEM micrograph of the tensile fractured surfaces showed the improvement of fiber-matrix adhesion after using SAH. The TGA results showed that chemical modification using SAH/DCP improved the thermal stability of the PBAT/EFB biocomposite. PMID:22343368

  15. Effect of nanofiller’s size and shape on the solid state microstructure and thermal properties of poly(butylene succinate) nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Papageorgiou, Dimitrios G.; Chrissafis, Konstantinos; Pavlidou, Eleni [Solid State Physics Section, Physics Department, Aristotle University of Thessaloniki, 541 24 Thessaloniki (Greece); Deliyanni, Eleni A.; Papageorgiou, George Z.; Terzopoulou, Zoi [Department of Chemistry, Aristotle University of Thessaloniki, 541 24 Thessaloniki (Greece); Bikiaris, Dimitrios N., E-mail: dbic@chem.auth.gr [Department of Chemistry, Aristotle University of Thessaloniki, 541 24 Thessaloniki (Greece)

    2014-08-20

    Highlights: • The microstructure and thermal properties of PBSu-based nanocomposites were studied. • Ag and SiO{sub 2} were dispersed more uniformly, compared to GO and MWCNTs. • PBSu/Ag nanocomposites exhibited higher nucleation activity and faster rates. • The order of nucleation efficiency of the fillers was GO < MWCNTs < SiO{sub 2} < Ag. • The activation energy of nanocomposite samples was lower than that of PBSu. - Abstract: We report a study of the solid state microstructure and crystallization kinetics of poly(butylene succinate) (PBSu) reinforced with nanofillers of different shapes, sizes and geometries such as silver, silica (SiO{sub 2}), multi-walled carbon nanotubes (MWCNTs) and graphene oxide (GO). The solid state structure of neat polymer and nanocomposites were investigated by X-ray diffraction (XRD), polarized optical microscopy (POM) and transmission electron microscopy (TEM). The results indicated that the nanocomposite samples exhibited enhanced crystallinity and nucleation density, along with smaller spherulite size. Additionally, the spherical nanofillers were dispersed more uniformly in the polymeric matrix, than the other two filler types. The crystallization kinetics under both isothermal and dynamic conditions were also studied and as was expected, the nanocomposite samples, crystallize at higher rates due to the increased number of nucleation sites, as was calculated with Avrami, Dobreva and Friedman’s methods. From the crystallization study it was found that the nanocomposite filled with Ag nanoparticles exhibited the highest rates from all other fillers followed from SiO{sub 2} and MWCNTs while GO showed the lowest rates.

  16. Modification of poly (butylene succinate-co-butylene adipate) (PBSA) by physical blending with poly (1,2-propylene succiate) (PPSu)%聚(丁二酸-1,2-丙二酯)(PPSu)对聚(丁二酸丁二酯-共聚-己二酸丁二酯)(PBSA)的物理改性的研究

    Institute of Scientific and Technical Information of China (English)

    王瑞冬; 徐军; 郭宝华

    2012-01-01

    聚(丁二酸丁二酯-共聚-己二酸丁二酯)(PBSA)是一种全生物降解材料,但由于其结晶度较高,无定形区比例较少,导致韧性不足.聚(丁二酸-1,2-丙二酯)(PPSu)是一种非结晶的生物可降解聚酯,在室温下处于无定型态.研究了PPSu对于PBSA的物理改性作用,通过DSC、DMA、POM、SEM测试对PBSA/PPSu的共混体系进行了表征,发现这2种脂肪族聚酯的共混物为部分相容体系,少量PPSu和PBSA相容.随PPSu质量分数的增加,共混体系玻璃化转变温度稍有升高,结晶速率下降.PPSu质量分数达10%时,断面刻蚀的SEM图片显示相分离结构.力学性能测试结果表明,在混入少量PPSu后,PBSA的抗冲击强度得到了较大提升.%Poly (butylene succinate-co-butylene adipate) (PBSA) is a kind of biodegradable material. However, due to its high degree of crystallinity and a low proportion of amorphou region,PBSA has low impact resistance. Poly( 1, 2-propylene succiate) (PPSu) is a kind of amorphous polymer,which can also be fully degraded in environment. In this study, PPSu is blended with PBSA. The miscibility, crystallization kinetics and the mechanical properties of the blends are investigated. Differential scanning caloreroetry, thermomechanical analysis, phase contrast optical microscopy and scanning electron microscopy have been adopted to study the miscibility of the two polymer components. The results show that PBSA and PPSu are miscible partially. When PPSu content is larger than 10 wt% , phase separation is observed in the blends. Increasing the amount of PPSu,the blends have higher glass transition temperature and slower crystallization rate. Compared with PBSA,the impact strength of the blends is greatly improved.

  17. Preparation of nanocomposites based on poly(Butylene Succinate) and montmorillonite organoclay via in situ polymerization; Preparo de nanocompositos de poli(succinato de butileno) (PDS) e argila motmorilonita organofilica via polimerizaco in situ

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Leticia P.; Moreira, Andrei N.; Souza Junior, Fernando G. de, E-mail: fgsj@ufrj.br [Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ (Brazil). Inst. de Macromoleculas; Pinto, Jose Carlos Costa da Silva [Coordenacao dos Cursos de Pos-Graduacao em Engenharia (COPPE/UFRJ), Rio de Janeiro, RJ (Brazil). Programa de Engenharia Quimica

    2014-09-15

    Nanocomposites based on poly(butylene succinate) (PBS) and organophilic montmorillonite were synthesized via in situ polymerization using three different clay compositions (4, 6 and 8 wt%). The products were characterized by several different techniques. X-ray diffraction was useful to confirm the increase of the interlayer spacing of the clay due to the presence of the polymer chains among layers. Thermal analysis indicated that the polymerization method chosen led to materials with lower thermal stability compared to the pure PBS, due to the difficulty of chain growth in the presence of the clay. Low-field NMR technique was used to assess clay dispersion in the polymer, with exfoliated structures predominating in the nanocomposites. (author)

  18. 丙烯-1-丁烯共聚BOPP结构及其薄膜拉伸工艺%Propylene-1-butylene copolymer structure and BOPP film stretching process

    Institute of Scientific and Technical Information of China (English)

    高达利; 张师军; 郭梅芳; 施红伟; 宋文波; 张丽英; 邹浩; 邵静波

    2015-01-01

    选取一种丙烯-1-丁烯共聚双向拉伸聚丙烯(BOPP)原料进行了薄膜双向拉伸加工实验,在不同工艺条件下制得BOPP薄膜,并对所制薄膜试样的拉伸过程、力学性能、光学性能等进行研究,建立了丙烯-1-丁烯共聚BOPP原料的薄膜拉伸工艺与薄膜拉伸成型和薄膜性能间的对应关系.研究表明:所采用的丙烯-1-丁烯共聚BOPP原料的拉伸成膜性好,拉伸工艺可调节范围宽.拉伸温度较高时薄膜的雾度升高,力学性能降低;而拉伸温度较低时,薄膜易出现拉伸不均匀的情况.此外,BOPP中丙烯-1-丁烯共聚结构的存在降低了薄膜结晶度,使得薄膜的光学性能较好.%A kind of biaxial oriented polypropylene(BOPP)of propylene-1-butylene copolymer was used to prepare BOPP film in different processing conditions. The stretching process,mechanical properties, optical properties of the film were studied. The relationships of the raw material stretching technology,film stretch forming and film properties were established.The results indicate that the BOPP has wider processing temperatures. The haze of the film increases and mechanical property decreases at higher stretching temperature,while the film becomes uneven at lower temperature. In addition,the crystallization degree of the film is decreased and the optical property is improved because of the existence of propylene-1-butylene copolymer.

  19. Biodegradation of poly(butylene succinate) powder in a controlled compost at 58°C evaluated by naturally-occurring carbon 14 amounts in evolved CO(2) based on the ISO 14855-2 method.

    Science.gov (United States)

    Kunioka, Masao; Ninomiya, Fumi; Funabashi, Masahiro

    2009-10-01

    The biodegradabilities of poly(butylene succinate) (PBS) powders in a controlled compost at 58 degrees C have been studied using a Microbial Oxidative Degradation Analyzer (MODA) based on the ISO 14855-2 method, entitled "Determination of the ultimate aerobic biodegradability of plastic materials under controlled composting conditions-Method by analysis of evolved carbon dioxide-Part 2: Gravimetric measurement of carbon dioxide evolved in a laboratory-scale test". The evolved CO(2) was trapped by an additional aqueous Ba(OH)(2) solution. The trapped BaCO(3) was transformed into graphite via a serial vaporization and reduction reaction using a gas-tight tube and vacuum manifold system. This graphite was analyzed by accelerated mass spectrometry (AMS) to determine the percent modern carbon [pMC (sample)] based on the (14)C radiocarbon concentration. By using the theory that pMC (sample) was the sum of the pMC (compost) (109.87%) and pMC (PBS) (0%) as the respective ratio in the determined period, the CO(2) (respiration) was calculated from only one reaction vessel. It was found that the biodegradabilities determined by the CO(2) amount from PBS in the sample vessel were about 30% lower than those based on the ISO method. These differences between the ISO and AMS methods are caused by the fact that part of the carbons from PBS are changed into metabolites by the microorganisms in the compost, and not changed into CO(2). PMID:20057944

  20. 高韧性PET/PBT合金的制备及性能%Preparation and Properties of Poly(Ethylene Terephthalate) / Poly(Butylene Terephthalate) Alloys with High Toughness

    Institute of Scientific and Technical Information of China (English)

    曹宇飞; 孙树林; 沙莎; 郭菲; 郝润佳; 张会轩

    2009-01-01

    甲基丙烯酸环氧丙酯接枝乙烯-辛烯共聚物(POE-g-GMA)用于聚时苯二甲酸乙二醇酯(PET)/聚对苯二甲酸丁二醇酯(PBT)共混物的增韧改性,同时考察了PET、PBT组成变化对共混体系性能的影响.结果表明,加入15%~20%(质量分数,下同)的POE-g-GMA共混体系发生脆韧转变,冲击强度最高可达890 J/m,实现超韧;基体的剪切屈服和橡胶粒子的空洞化是增韧PET/PBT共混物主要形变机理.%Glycidyl methacrylate grafted poly(ethylene octane) copolymer (POE-g-GMA) was used as modifiers to improve the toughness of poly(ethylene terephthalate) (PET)/Poly (butylene terephthalate) (PBT) blends. The influence of PET and PBT ratio change on the properties of the blends was investigated. The results show that brittle-ductile transition takes place with 15%~20% POE-g-GMA addition. Impact strength value of 890 J/m is achieved which displays the super-toughness. Shear yielding of matrix and cavitation of rubber particles are the major toughening mechanisms of the rubber toughened PET/PBT blends.

  1. The Influence of Green Surface Modification of Oil Palm Mesocarp Fiber by Superheated Steam on the Mechanical Properties and Dimensional Stability of Oil Palm Mesocarp Fiber/Poly(butylene succinate Biocomposite

    Directory of Open Access Journals (Sweden)

    Yoon Yee Then

    2014-08-01

    Full Text Available In this paper, superheated steam (SHS was used as cost effective and green processing technique to modify oil palm mesocarp fiber (OPMF for biocomposite applications. The purpose of this modification was to promote the adhesion between fiber and thermoplastic. The modification was carried out in a SHS oven at various temperature (200–230 °C and time (30–120 min under normal atmospheric pressure. The biocomposites from SHS-treated OPMFs and poly(butylene succinate (PBS at a weight ratio of 70:30 were prepared by melt blending technique. The mechanical properties and dimensional stability of the biocomposites were evaluated. This study showed that the SHS treatment increased the roughness of the fiber surface due to the removal of surface impurities and hemicellulose. The tensile, flexural and impact properties, as well as dimensional stability of the biocomposites were markedly enhanced by the presence of SHS-treated OPMF. Scanning electron microscopy analysis showed improvement of interfacial adhesion between PBS and SHS-treated OPMF. This work demonstrated that SHS could be used as an eco-friendly and sustainable processing method for modification of OPMF in biocomposite fabrication.

  2. 聚丁二酸丁二醇酯环状二聚物的纯化、表征及其开环聚合%Purification, Characterization and Ring-opening Polymerization of Cyclic Dimer of Poly (butylenes succinate)

    Institute of Scientific and Technical Information of China (English)

    杨群; 崔进; 陆大年

    2013-01-01

    从聚丁二酸丁二醇酯(PBS)的环状低聚物中分离提纯出了PBS的环状二聚物[cyclic dimer of poly(butylene succinate),CDBS],采用核磁、质谱对该环状二聚物进行了表征,研究表明,通过分离纯化得到了纯度高的PBS的环状二聚物.以纯化的CDBS为原料、十二醇为初始剂、辛酸锡作催化剂,采用开环聚合的方法合成了PBS,采用核磁、红外光谱对合成的PBS的结构进行了表征,并研究了开环聚合温度、聚合时间以及催化剂用量对PBS的分子量、单体转化率的影响,结果表明,开环反应温度220℃左右,反应3h,PBS的相对分子质量(简称分子量,下同)可达到63 300,与直接酯化-缩聚法相比,采用开环聚合法能提高PBS的制备效率.

  3. The influence of green surface modification of oil palm mesocarp fiber by superheated steam on the mechanical properties and dimensional stability of oil palm mesocarp fiber/poly(butylene succinate) biocomposite.

    Science.gov (United States)

    Then, Yoon Yee; Ibrahim, Nor Azowa; Zainuddin, Norhazlin; Ariffin, Hidayah; Yunus, Wan Md Zin Wan; Chieng, Buong Woei

    2014-01-01

    In this paper, superheated steam (SHS) was used as cost effective and green processing technique to modify oil palm mesocarp fiber (OPMF) for biocomposite applications. The purpose of this modification was to promote the adhesion between fiber and thermoplastic. The modification was carried out in a SHS oven at various temperature (200-230 °C) and time (30-120 min) under normal atmospheric pressure. The biocomposites from SHS-treated OPMFs and poly(butylene succinate) (PBS) at a weight ratio of 70:30 were prepared by melt blending technique. The mechanical properties and dimensional stability of the biocomposites were evaluated. This study showed that the SHS treatment increased the roughness of the fiber surface due to the removal of surface impurities and hemicellulose. The tensile, flexural and impact properties, as well as dimensional stability of the biocomposites were markedly enhanced by the presence of SHS-treated OPMF. Scanning electron microscopy analysis showed improvement of interfacial adhesion between PBS and SHS-treated OPMF. This work demonstrated that SHS could be used as an eco-friendly and sustainable processing method for modification of OPMF in biocomposite fabrication. PMID:25177865

  4. Ti-MSU分子筛催化1-丁烯氧化制环氧丁烷的研究%Research on Epoxybutane from 1-Butylene by Ti-MSU Molecular Sieve Catalytic Oxidation

    Institute of Scientific and Technical Information of China (English)

    吴美玲; 周灵杰; 陈玮娜

    2014-01-01

    通过液相浸渍法制备Ti 质量分数为5�5%的Ti-MSU分子筛催化剂,并采用X射线衍射、N2吸附-脱附对催化剂样品进行表征。考察了Ti-MSU催化剂对以过氧化氢异丙苯( CHP)、1-丁烯为原料制备环氧丁烷的反应工艺条件的影响。结果表明,当催化剂床层温度为100℃、反应压力为3�0 MPa、1-丁烯/CHP摩尔比为10∶1、CHP空速为2 h-1时,CHP的转化率达到81�2%,1,2-环氧丁烷( BO)选择性为60�2%,苄醇( DMBA)选择性为87�2%。%5.5%Ti-MSU molecular sieve catalyst was prepared by liquid phase impregnation method. The sam-ple was characterized by X-ray diffraction and N2 adsorption-desorption. With cumene hydroperoxide ( CHP) ,1-bu-tene as raw material,the influence of the process conditions of 5.5%Ti-MSU catalyst on epoxybutane had been in-vestigated. The conversion of CHP was 81.2%,1,2-epoxybutane ( BO) selectivity was 60.2%, benzyl alcohol ( DMBA) selectivity was 87.2%, when the optimum reaction conditions was 100℃ catalyst bed,3.0 MPa reactivity pressure,10∶1 1-butylene/CHP molar ratio and 2h-1 space velocity of CHP.

  5. Biodegradation of Poly(butylene succinate Powder in a Controlled Compost at 58 °C Evaluated by Naturally-Occurring Carbon 14 Amounts in Evolved CO2 Based on the ISO 14855-2 Method

    Directory of Open Access Journals (Sweden)

    Masahiro Funabashi

    2009-09-01

    Full Text Available The biodegradabilities of poly(butylene succinate (PBS powders in a controlled compost at 58 °C have been studied using a Microbial Oxidative Degradation Analyzer (MODA based on the ISO 14855-2 method, entitled “Determination of the ultimate aerobic biodegradability of plastic materials under controlled composting conditions—Method by analysis of evolved carbon dioxide—Part 2: Gravimetric measurement of carbon dioxide evolved in a laboratory-scale test”. The evolved CO2 was trapped by an additional aqueous Ba(OH2 solution. The trapped BaCO3 was transformed into graphite via a serial vaporization and reduction reaction using a gas-tight tube and vacuum manifold system. This graphite was analyzed by accelerated mass spectrometry (AMS to determine the percent modern carbon [pMC (sample] based on the 14C radiocarbon concentration. By using the theory that pMC (sample was the sum of the pMC (compost (109.87% and pMC (PBS (0% as the respective ratio in the determined period, the CO2 (respiration was calculated from only one reaction vessel. It was found that the biodegradabilities determined by the CO2 amount from PBS in the sample vessel were about 30% lower than those based on the ISO method. These differences between the ISO and AMS methods are caused by the fact that part of the carbons from PBS are changed into metabolites by the microorganisms in the compost, and not changed into CO2.

  6. 热塑性淀粉/PBS共混物的微生物降解性研究%Biodegradation of starch/poly(butylene succinate) blends by the selected cultured fungi

    Institute of Scientific and Technical Information of China (English)

    李陶; 李辉章; 曾建兵; 王玉忠

    2009-01-01

    In recent years,much progress has been achieved in the development of biodegradable products using agricultural materials as basis,for the environmental threats restrict the use of non-degradable polymers.In order to obtain a cost-effective biodegradable plastic,a novel environmental-friendly starch/poly(butylene succinate) (PBS) blends with improved compatibility were successfully prepared using glycerol as plasticizer.In this work,the biodegradation behavior of starch/PBS blends was studied by the selected cultured fungi according to the ISO846-1997.The ultimate biodegradation percentage revealed that the blends showed good biodegradability.Rates of weight loss increased with the decrease of PBS contents or the increase of the molecular weight of PBS,which is ascribed to the fact that the dispersed PBS blocked the fungi to attack starch matrix.Moreover,the presence of plasticizer such as glycerol can further influence the biodegradation percentage.For all samples,the weight loss was accompanied by a rapid deterioration in tensile strength and elongation at break.In addition,biodegradation resulted in an increase of crystallinity and melting point in starch/PBS blends.%以甘油作为增塑剂,采用玉米淀粉与改性后的聚丁二酸丁二醇酯(PBS)熔融共混制备出淀粉/PBS共混材料.对这种改善了两相相容性的共混材料在特定微生物条件下的降解行为进行了研究.结果显示,共混物降解28天后,含有30%PBS的共混物质量损失达到35%左右,其力学性能只有降解前的20%,甘油含量减小和PBS含量增加均能减缓材料的降解.且随着降解时间的延长,PBS的结晶度和熔点有所提高.

  7. Fungi screening and degradation characteristics for efficient poly(butylenes succinate)degradation%聚丁二酸丁二醇酯高效降解菌的筛选及降解特性

    Institute of Scientific and Technical Information of China (English)

    梅雪立; 梁英梅; 田呈明; 董骞; 孙琪

    2011-01-01

    A fungal strain BFM-X1 was isolated from air environment on vegetable field, which had a strong ability to degrade poly (butylenes succinate, PBS). Morphological and phylogenetic analysis revealed that strain BFM-X1 was closely related to Bionectria ochroleuca. The optimum temperature for strain BFM-X1 degrading PBS film ranged from 25 ℃ to 30 ℃ and the initial pH of medium was 4.0. A high degradation rate for PBS film was observed with glucose, glycerole, soybean oil or PBS emulsion as a single carbon source for this strain. The curve of PBS film degradation rate with the increase of the PBS emulsion concentration showed a resupinate "U", and the optimum PBS emulsion concentration was 1 g/L. Three phases were exhibited during PBS degradation by BFM-X1. Scanning electron micrographs showed that the surface of PBS film firstly became rough, then some holes appeared on the PBS film and the PBS film gradually disintegrated, at last the PBS film completely degraded.%从蔬菜地表微环境空气微生物中分离筛选获得了一株高效降解聚丁二酸丁二醇酯(PBs)的真菌菌株BFM-X1,通过形态学和ITS rDNA序列测定分析,确认该菌株为淡色生赤壳属真菌(Bionectria ochroleuca).该菌株降解PBS薄膜的最适温度为25℃-30℃,培养基初始pH为4.0,以甘油、大豆油、葡萄糖及PBS乳剂分别作为唯一碳源时对PBS薄膜均具有很高的降解率;菌株对PBS薄膜的降解率随PBS乳剂含量变化的曲线呈倒"U"型,最佳PBS乳剂浓度为1g/L,且对PBS的降解呈现诱导期、指数降解期和加速降解期等3个阶段.降解初期薄膜表面首先粗糙化,失去原有的黑色光泽,随后出现孔洞,逐渐呈现破碎化,最后薄膜被完全降解,降解部位仅残留黑色色素.

  8. Denitrification of saline water with poly butylene succinate as carbon source and biofilm carriers%以聚丁酸丁二醇酯为碳源去除含盐水体硝酸盐的研究

    Institute of Scientific and Technical Information of China (English)

    罗国芝; 董明来; 刘倩; 邓棚文; 谭洪新

    2013-01-01

    以可生物降解聚合物为碳源和生物膜载体可以解决异养反硝化有机碳源的添加不足或过量的问题.在序批式反应条件下,以聚丁酸丁二醇酯(PBS)为碳源和生物膜载体,对含盐水体异养反硝化过程中的细菌群落特征进行了研究.结果表明,试验条件下硝酸盐可以得到很好的去除,虽然有亚硝酸盐的明显积累,但最终被降低.硝酸盐的存在会降低含PBS水体中溶解性有机物的含量.应用变性梯度凝胶电泳和16S rDNA的方法鉴别到的细菌包括:Pseudomonas stutzeri,Pseudomonas sp.,Alteromonas sp.,Marinobacter salsuginis,Thalassospira xianheensis,Itellibacter vladivostokensis,Euplotopsis encysticus,Alcanivorax venustensis,Halomonas sp.,Agrobacterium tume aciens,Pannonibacter phragmitetus,Vitellibacter vladivostokensis.试验结果表明,反硝化条件下PBS具有较好的可生物降解性和明显的NO3--N去除能力,是比较理想的低C/N含盐水体异养反硝化碳源.%The problem of improper addition of organic carbon source in heterotrophic denitrification process could be well solved by using biodegradable polymer as both solid carbon source and biofilm carriers. Batch experiments were carried out to use poly butylene succinate (PBS) as solid carbon source and biofilm carriers to remove nitrate-nitrogen from saline wastewater. The bacterial community was identified using denaturing gradient gel electro-phoresis (DGGE) and 16S rDNA sequencing. The results showed that large amount of nitrate was removed under the experiment condition, although the obvious nitrite accumulation was found during denitrification process, but they eventually be removed. The existence of nitrate could reduce the content of dissolving organic matter in PBS containing wastewater. The bacteria found in bioreactor were assigned to Pseudomonas stutzri, Pseudomonas sp. , Alteromonas sp. ,Marinobacter salsuginis , Thalassospira xianheensis , Itellibacter vladivostokensis

  9. 静电纺丝素/聚丁二酸丁二醇酯血管材料的结构与性能%Structure and properties of electrospun silk fibroin-poly( butylene succinate) artificial blood vessel

    Institute of Scientific and Technical Information of China (English)

    吴斌伟; 朱海霖; 张乐伟; 冯新星; 陈建勇

    2011-01-01

    为制备组织工程血管支架,以丝素蛋白(SF)和聚丁二酸丁二醇酯(PBS)为原料,通过静电纺丝法,以具有三维结构的收集模板取代传统的二维平板作为静电纺丝收集基板,构建丝素/PBS血管支架材料.研究纺丝条件和三维收集模板对管状支架形貌的影响,采用FT-IR对丝素蛋白二级结构进行表征,测试血管支架材料的孔隙率和力学性能.结果表明,通过改变电压、纺丝间距以及三维收集模板的宏观结构,可制备出具有不同直径和长度的血管支架材料.这种支架材料的孔隙率达84.6%,拉伸应力为4.31 MPa,断裂伸长率为46.21%,爆破压力为358kPa.%To develop a small-diameter tissue engineering blood vessel, the silk fibroin (SF)/poly( butylene succinate) (PBS) tubular scaffolds were fabricated via electrospinning. During the electrospinning process, the electrospun SF/PBS composite tubular scaffolds were collected on a 3-D collector instead of traditional 2-D collector. The effects of 3-D collector and process parameters of electrospinning on the morphologies of the tubular scaffolds were investigated. FT-IR was used to study the secondary structure of SF. The mechanical properties and porosities of the tubular fiber materials were characterized. The results showed that SF/PBS composite tubular materials with different sizes and shapes could be prepared by changing the voltage, TCD and the structure of 3-D collectors. The porosity, tensile stress, elongation at break and burst pressure of the composite tubular scaffold were 84. 6%, 4. 31 MPa,46. 21% and 358 kPa, respectively.

  10. Catalytic Effects Comparison of Several Catalysts Used to Synthesize Poly (Butylene Succinate)%几种合成聚丁二酸丁二酯用催化剂的催化效果比较

    Institute of Scientific and Technical Information of China (English)

    高艳; 赖仕全; 刘兴南; 岳莉; 赵雪飞

    2014-01-01

    Poly(butylene succinate) (PBS) was synthesized respectively from 1,4-succinic acid and 1,4-butanediol using SnCl2,Sn(Oct)2,ZnCl2,Zn(OAc)2,Sb2O3 or SO42-/ZrO2 as catalyst by direct melt polycondensation method. The catalytic effects of the 6 kinds of catalysts in the polymerization reaction of PBS were compared by measuring liquid yield in the esterification reaction stage,yield and properties of PBS,such as intrinsic viscosity,molecular weight and melting temperature. Taking SnCl2 as example, the structure and thermal stability of PBS synthesized by SnCl2 were studied with FTIR and TG. The results show that the synthesized product is hydroxyl-capped PBS. The 6 kinds of catalysts all can promote dehydration esterification reaction of 1,4-succinic acid and 1,4-butanedio. Except for Sn(Oct)2,several other catalysts can effectively reduce the formation of tetrahydrofuran by-product. Overall,the catalytic effects of stannum compound are best among these catalyst and when SnCl2 is used as catalyst,the yield, intrinsic viscosity,number average molecular weight and original melting temperature of the synthesized PBS are best and it’s decomposition temperature is 280℃. Taking molecular weight of PBS as index,the order of the catalytic effects of the 6 catalysts is SnCl2>Sn(Oct)2>Sb2O3>SO42-/ZrO2>ZnCl2>Zn(OAc)2.%以1,4-丁二酸和1,4-丁二醇为原料,分别以SnCl2,异辛酸亚锡[Sn(Oct)2],ZnCl2,乙酸锌[Zn(OAc)2], Sb2O3和SO42-/ZrO2固体超强酸为催化剂,采用直接熔融缩聚法合成了聚丁二酸丁二酯(PBS)。通过测试酯化反应阶段的出液量、PBS的收率及其特性黏度、数均分子量和熔融温度等性质,比较了6种催化剂在PBS聚合反应中的催化效果。以SnCl2为例,利用傅立叶变换红外光谱和热重分析研究了由其催化合成的PBS的结构和热稳定性能。结果表明,实验合成的产物为羟基封端PBS;6种催化剂都能促进1,4-丁二酸和1,4-丁二醇分子间

  11. 一种新型聚对苯二甲酸丁二醇酯-层状硅酸盐纳米复合材料的制备与性能%Preparation and Properties of a New Type of Poly (butylene-terephthalate) with Layered Silicate Nanocomposites

    Institute of Scientific and Technical Information of China (English)

    柯扬船

    2003-01-01

    In this paper, poly(butylene-terephthalate)-layered silicate of clay nanocomposites (NPBT) are reported. Their thermal properties, heat distortion temperature (HDT) and crystallization nucleation are investigated. NPBT samples have apparent viscosity over 0.85, HDT of 30℃ to 50℃ higher than that of poly (butyleneterephthalate) (PBT) for clay load from 1.0% to 10.0% (by mass), and higher capability to accommodate clay than other polymers. The nonisothermal crystallization experiments indicate that the better thermal degradation behavior and crystallization rate of NPBT are 50% higher than PBT, and its injection mould processing temperature is lowered from 110℃ to 55℃. NPBT samples are characterized by several techniques. X-ray shows an original clay interlayer distance enlarged from 1.0 nm to 2.5 nm, while both TEM and AFM indicate an average size from 30nm to 100nm of exfoliated clay layers, and 3%(by mass) of particle agglomeration being phase separated from PBT matrix, which are factors on some mechanical properties decrease of NPBT. The disappearance of spherulitic morphology in NPBT resulted from layers nucleation is detected. Improving NPBT properties by treating clay with long chain organic reagent and controlling the way to load it is suggested.

  12. 1,4-环己烷二甲醇改性生物可降解聚酯PBS的合成与性能表征%Synthesis and Characterization of Biodegradable Poly butylenes succinate Modified by 1,4-Cyclohexane Dimethanol

    Institute of Scientific and Technical Information of China (English)

    李修莲; 周艺峰; 聂王焰; 宋林勇

    2012-01-01

    A series of poly(butylene succinate-co-1,4-cyclohexane dimethanol succinate) random copolyes- ters were synthesized by melt polycodensation. The structure and physical properties of the aliphatic poly- esters were characterized by hydrogen nuclear magnetic resonance spectrum (1 H-NMR), Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), thermogravimetry analysis (TGA), X-ray diffraction (XRD) and lipase enzymatic degradation test. Results show that the synthetic copolyesters are the expected products, the crystal structure of copolyesters has been changed and the cocrystallization behavior has appeared. The melting point of the product decreases from 113.7 ℃ to 64.6℃, and then increases to 114.2 ℃. Moreover, the glass transition temperature increases monotonously from -33.8 ℃ to 5.4 ℃ along with the increasing of 1,4-cyclohexane dimethanol succinate (CHDM) component. With the increasing of 1,4-cyclohexane dimethanol component, the eopolyesters have better thermal stability. The lipase enzymatic degradation tests indicate that the copolyesters PS1 and P31 have better degradability, and P51 has the fastest degradation.%用熔融缩聚法合成了一系列聚(丁二酸丁二醇酯丁二酸-1,4-环己烷二甲醇酯)无规共聚物。通过。H—NMR、FT—IR、DSC、TGA、XRD、酶降解测试等方法表征了材料的结构与性能。结果表明:合成得到的共聚酯为预期产物;共聚酯的晶体结构发生了改变,并产生了共晶行为;随着1,4-环己烷二甲醇(CHDM)含量的增加,产物的熔点由113.7℃降至64.6℃,然后升至114.2℃,玻璃化转变温度由-33.8℃单调升高至5.4℃;CHDM的引入增强了共聚酯的热稳定性;酶降解测试得出产物P51、P31具有良好的生物降解性,且P51降解最快。

  13. Hidrofilicidade de filmes de amido/poli(butileno adipato co-tereftalato (Pbat adicionados de tween 80 e óleo de soja Hydrophilicity of starch and poly(butylene adipate-co-terephthalate (Pbat films containing tween 80 and soybean oil

    Directory of Open Access Journals (Sweden)

    Renata P. Herrera Brandelero

    2013-01-01

    Full Text Available A incorporação de amido ao polímero poli (butilenoadipatoco-tereftalato (PBAT através de blendas com alto teor de amido pode ser uma alternativa para obter embalagens biodegradáveis, minimizar custos e o uso de recursos não renováveis. No entanto, a adição de amido aumenta a permeabilidade ao vapor de água (PVA. A incorporação em filmes com amido de substâncias como óleos vegetais e surfactantes pode diminuir a hidrofilicidade, favorecendo as aplicações destes como embalagens. A hidrofilicidade dos filmes elaborados por blendas de amido/PBAT adicionados de óleo de soja (OS e tween 80 (TW foi avaliada considerando o efeito do OS e TW nas isotermas de sorção dos filmes, na PVA e nos coeficientes de difusão (Dw e solubilidade (β do vapor de água. Filmes com OS com ou sem TW apresentaram menor quantidade de água de sorção, sendo os filmes com menores quantidades de OS e sem TW menos hidrofílicos e menos permeáveis aos vapores de água. A adição de OS reduziu os valores de β e Dw dos filmes de amido/PBAT. O efeito foi relacionado com o aumento das porções hidrofóbicas e da compatibilidade entre o amido e PBAT na presença de OS.Incorporating starch into the poly(butylene adipate-co-terephthalate (PBAT polymer by means of blends with high starch contents is a possible option for producing biodegradable packaging using renewable resources and reducing costs. However, the addition of starch increases the water vapour permeability (WVP. The incorporation of substances as lipids and surfactants can reduce the hydrophilicity of films containing starch, favouring their use as packaging. The hydrophilicity of films produced from blends of starch/PBAT with added soybean oil (SO and tween 80 (TW was studied. The effects of these substances on the sorption isotherm, on the WVP and on the water vapour diffusion (Dw and solubility (β coefficients of the films were evaluated. The water sorption in films with SO, with or without TW

  14. 高剪切应力对苯乙烯-乙烯/丁烯-苯乙烯三嵌段聚合物马来酸酐化反应的影响%Influence of high shear stress on functionalization of maleic anhydride with styrene-ethylene/butylene-styrene terblock polymer

    Institute of Scientific and Technical Information of China (English)

    杜丽; 张玲; 张云灿

    2013-01-01

    The functionalization reaction of styrene-ethylene/butylene-styrene terblock polymer (SEBS) with maleic anhydride (MAH) was investigated through the high shear stress-induced initiation by increasing the screw rotation speed of twin-screw extruder.The results showed that the percent of grafting and the melt flow rate of functionalized products (SEBS-g-MAH) increased obviously with the increase of screw rotation speed,indicating that the high shear stress produced by increasing screw rotation speed led to the chain scission and the macro-radical,thus initiating the grafting reaction between SEBS and MAH.The crosslinking reaction could be effectively suppressed through increasing screw rotation speed to prepare the functionalized product SEBS-g-MAH with higher percent of grafting (mass fraction 0.79%-0.89%) and appropriate melt flow rate (1.859-4.398 g/min) and lower gel content (no more than mass fraction 0.32%).Meanwhile,the toughening effect of SEBS-g-MAH on nylon (PA 66) was much better.The Izod notched impact strength of the blend reached up to 94 kJ/m2,which was 30 times more than that of pure PA 66 without significant decrease of tensile and flexural strengthes.%通过提高双螺杆挤出机螺杆转速的应力引发方法,研究了高剪切应力下马来酸酐(MAH)与苯乙烯-乙烯/丁烯-苯乙烯三嵌段聚合物(SEBS)的官能化反应.结果表明,随着双螺杆挤出机螺杆转速的提高,官能化产物的接枝率和熔体流动速率明显增大.高剪切应力的作用引起大分子链断链,形成大分子自由基,从而引发SEBS的接枝反应.通过提高螺杆转速可有效地抑制交联副反应,制得接枝率较高(质量分数0.79%~0.89%)、熔体流动速率适宜(1.859 ~4.398 g/min)和凝胶含量较低(质量分数不大于0.32%)的官能化产物.同时,由应力诱导引发所得官能化产物SEBS-g-MAH对尼龙(PA 66)的增韧效果较好,其共混物的悬臂梁缺口冲击强度能达到约94 kJ/m2,

  15. INVESTIGATION ON CRYSTALLIZATION AND MECHANICAL PROPERTIES OF POLY( BUTYLENE SUCCINATE)/NANO KAOLIN BLENDS%聚丁二酸丁二酯/纳米高岭土共混体系结晶及力学性能研究

    Institute of Scientific and Technical Information of China (English)

    唐义祥; 楼白杨; 梁多平

    2011-01-01

    用熔融共混法制备聚丁二酸丁二酯(PBS)/纳米高岭土(nano kaolin)复合降解材料,利用FTIR、DSC、万能拉力机和SEM对其微观结构、结晶、力学性能及分散性进行研究.FTIR光谱分析结果表明,改性剂与nano kaolin发生了化学键合作用;DSC结果表明,在PBS中加入nano kaolin,提高了结晶起始(T0,c)、结晶峰(Tp,c)以及结晶结束温度(Te,c),结晶度随着nano kaolin的增加呈先增大后下降的趋势,另外通过二次升温曲线发现PBS/nano kaolin复合材料存在双重熔融行为即存在低温峰L和高温峰H;力学性能测试表明,PBS/nano kaolin复合降解材料中nano kaolin添加量较少时,材料的缺口冲击性能、断裂伸长率和拉伸强度有明显的改善;SEM结果表明,添加的少量nano kaolin可以均匀的分散在PBS树脂中,但其含量较高时会有明显的团聚的现象.综上述结果表明,在PBS中添加适量的nano kaolin能显著提高PBS的结晶和力学性能.%In order to improve the performance of poly( butylenes succinate) (PBS) like the crystallinity and mechanical properties, PBS/nano kaolin blends were prepared by mechanical melting mixing. The microstructure, crystallinity, mechanical properties and dispersion of the PBS/nano kaolin were studied respectively with infrared spectrometer ( FTIR ), differential scanning calorimeter ( DSC ), universal material testing machine and scanning electron microscope ( SEM ). Infrared spectra showed picture shown that the modifier could be bonded to nano kaolin. The DSC results indicated that the onset ( denoted as To .c ), peak (denoted as Tp .c ) and end crystallization temperature (denoted as Te .c) of PBS were increased respectively.DSC melting curves for the melt-crystallized samples were obtained at 10 K min-1. Double endothermic peaks,a high-temperature peak H and a low-temperature peak L, and an exothermic peak located between them appeared. At the same time, the crystallization degree rose first

  16. 21 CFR 172.712 - 1,3-Butylene glycol.

    Science.gov (United States)

    2010-04-01

    ...: (a) It is prepared by the aldol condensation of acetaldehyde followed by catalytic hydrogenation. (b... reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies are available from the Office...

  17. Investigation on mechanical properties, rheological behavior and degradation performance of poly(butylenes succinate)/poly(3-hydroxybutyrate-co-4-hydroxybutyrate)/nano Kaolin blends%聚丁二酸丁二酯/聚(3-羟基丁酸酯-co-4-羟基丁酸酯)/纳米高岭土熔融共混力学性能、流变及降解行为研究

    Institute of Scientific and Technical Information of China (English)

    唐义祥; 孙万里; 何宏; 梁多平

    2013-01-01

    用熔融共混挤出法制备的聚丁二酸丁二酯(PBS)/聚(3-羟基丁酸酯co-4-羟基丁酸酯)[poly (3 HB-co-4 HB)]/纳米高岭土(nano Kaolin)复合降解材料;利用万能拉力机、旋转流变仪和SEM对其力学性能、流变行为、微观结构及降解性能进行研究.结果表明,PBS/poly(3HB co-4HB)/nano Kaolin(100/10/8)复合降解材料的缺口冲击强度、断裂伸长率达到最大,此后随着nano Kaolin质量百分比增加,而呈下降趋势;在室外自然条件下,经过土埋一段时间后的降解实验,PBS/poly(3 HB-co-4 HB)/nano Kaolin(100/10/12)复合材料发生了明显的降解,复合降解材料的失重率也已经降到64%左右,说明材料的降解性能较好;纳米复合降解材料熔融剪切储能模量(G'),剪切损耗模量(G")随着频率的增大呈单增趋势.%In order to improve the combinatorial performance of poly ( butylenes succinate) (PBS)/poly (3-hydroxybutyrate-co-4-hydroxybutyrate)(poly(3HB-co-4HB)) like the mechanical properties and rheological be-haviors, PBS/poly(3HB-co-4HB)/nano Kaolin blends were prepared by mechanically melting mixing. The me-chanical and degradation properties and rheological behaviors of the PBS/poly(3HB-co-4HB)/nano Kaolin were studied respectively with universal material testing machine, rheometer and scanning electron microscope (SEM). The mechanical properties testing of universal material testing machine shown that the relative mass ratio of nano Kaolin was 8, the notched impact strength and elongation at break of PBS/poly (3HB-co-4HB)/ nano Kaolin blends were improved obviously. However,the relative mass ratio of nano Kaolin increased, their properties decreased in a way. At the same time, the tensile strengths of PBS/poly (3HB-co-4HB)/nano Kaolin blends were declined clearly. The rheology experiments indicated the storage modulus (G') and loss modulus (G") increased significantly with the increase of frequency. The SEM shown that degradation performances

  18. Aerogel Poly(butylene succinate) Biomaterial Substrate for RF and Microwave Applications

    Science.gov (United States)

    Habib Ullah, M.; Mahadi, W. N. L.; Latef, T. A.

    2015-08-01

    Polybutylene succinate (PBS) has become a potential candidate, similar to polypropylene (PP) and acrylonitrile butadiene styrene (ABS), for use as an organic plastic material due to its outstanding mechanical properties as well as high thermal deformation characteristics. A new composition of silica aerogel nanoparticles extracted from rice waste with PBS is proposed for use as a dielectric (ɛr = 4.5) substrate for microwave applications. A microstrip patch antenna was fabricated on the proposed dielectric substrate for multi-resonant ultra-wideband (UWB) applications. The performance characteristics of the proposed biomaterial-based antenna were investigated in a far-field measurement environment. The results indicate that the proposed biocompatible material-based antenna covered a bandwidth of 9.4 (2.3-11.7) GHz with stop bands from 5.5 GHz to 5.8 GHz and 7.0 GHz to 8.3 GHz. Peak gains of 9.82 dBi, 7.59 dBi, 8.0 dBi and 7.68 dBi were measured at resonant frequencies of 2.7 GHz, 4.6 GHz, 6.3 GHz and 9.5 GHz, respectively.

  19. Structural relaxation accompanied by photo-induced chromatic phase transition of polydiacetylenes with butylene-N-difluorophenyl carbamate side chains

    Energy Technology Data Exchange (ETDEWEB)

    Maekawa, Yuuki; Sakamoto, Naoya; Kokado, Ryousuke; Kajimoto, Naoshi; Izumi, Yuuichiro [Department of Materials Science and Chemistry, Wakayama University, 930 Sakaedani, Wakayama (Japan); Itoh, Chihiro, E-mail: citoh@sys.wakayama-u.ac.jp [Department of Materials Science and Chemistry, Wakayama University, 930 Sakaedani, Wakayama (Japan)

    2013-01-15

    We have studied the phase transition of poly-5,7-dodecadiyne-1,12-diol bis[2,4-difluorophenyl carbamate] (PDA-2,4-DFPC) and poly-5,7-dodecadiyne-1,12-diol bis[3,4-difluorophenyl carbamate] (PDA-3,4-DFPC) by visible reflection spectroscopy and mid-infrared absorption spectroscopy. Both PDA-2,4-DFPC and PDA-3,4-DFPC show the reflection spectra characterized by a sharp peak at around 1.9 eV at room temperature. While PDA-3,4-DFPC shows thermochromic phase transition to the phase showing the reflection spectrum with a peak around 2.2 eV above 120 Degree-Sign C, PDA-2,4-DFPC shows no abrupt change of the reflection spectrum. However, PDA-2,4-DFPC shows drastic change of the reflection spectrum under 532-nm CW-laser excitation. Based on these results, we can draw the following two conclusions. First, the phase transition behavior of PDA can be controlled by modifying the side-chain structure. Second, we demonstrate that thermally inaccessible phase of PDA is induced by the photo-excitation. By measuring mid-infrared absorption of PDAs, we elucidated that conformational change of side chains is accompanied with the phase transition. Based on the results, we discussed the role of the side chain in the phase transition. - Highlights: Black-Right-Pointing-Pointer We have synthesized polydiacetylene (PDA) with difluorophenyl carbamate side chain. Black-Right-Pointing-Pointer PDAs show distinct phase transition (PT) depending on the side-chain structure. Black-Right-Pointing-Pointer PDA with 3,4-difluorophenyl carbamate shows PT by thermal stimulation. Black-Right-Pointing-Pointer However, PDA with 2,4-difluorophenyl carbamate shows PT only under photo-excitation.

  20. Biodegradation of poly(lactic acid) and poly(butylene succinate-co-adipate) by Paenibacillus amylolyticus strain TB-13

    OpenAIRE

    Teeraphatpornchai, Teerawat

    2003-01-01

    Polymer materials developed during the last 80 years are generally resistant to microbial attack, a property that is now currently regarded as a shortcoming concerning solid waste management. As a source of alternative environmental friendly materials, the synthesis of degradable polymers is becoming of considerable interest.Recently, increasing iterest has been devoted to understanding the degradation mechanisms of polymers in the environment. A number of synthetic polymers have been referre...

  1. The effect of chitosan on the in vitro biological performance of chitosan-poly(butylene succinate) blends

    OpenAIRE

    Coutinho, Daniela F.; Pashkuleva, I.; Alves, Catarina M.; Marques, A.P.; Neves, N. M.; Reis, R. L.

    2008-01-01

    Chitosan blends with synthetic biodegradable polymers have been proposed for various biomedical applications due to their versatile mechanical properties and easier processing. However, details regarding the main surface characteristics that may benefit from the blending of these two types of materials are still missing. Hence, this work aims at investigating the surface properties of chitosan-based blends, illustrating the way these properties determine the material-proteins inte...

  2. Synthesis and characterization of polyester copolymers based on poly(butylene succinate) and poly(ethylene glycol)

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Xiao-Ming, E-mail: xiaomingzhou@tust.edu.cn

    2012-12-01

    A series of polyester copolymers was synthesized from 1,4-succinic acid with 1,4-butanediol and poly(ethylene glycol) through a two-step process of esterification and polycondensation in this article. The composition and physical properties of copolyesters were investigated via GPC, {sup 1}HNMR, DSC and PLM. The copolymer composition was in good agreement with that expected from the feed composition of the reactants. The melting temperature (T{sub m}), crystallization temperature (T{sub c}), and crystallinity (X{sub c}) of these copolyesters decreased gradually as the content of PEG unit increased. Otherwise, experimental results also showed that the contents of PEG in copolymers had an effect on the molecular weight, distribution, thermal properties, hydrolysis degradation properties, and crystalline morphology of polyester copolymers. - Graphical abstract: The composition of polyester copolymer was determined from the {sup 1}H NMR spectra using the relative intensities of the proton peaks. As a sample, the {sup 1}H NMR spectrum of polyester copolymer with 10 mol% of PEG is shown in Fig. 2: CO-(CH{sub 2}){sub 2}-CO; O-CH{sub 2}- and C-(CH{sub 2}){sub 2}-C from the SA and BD unit at {delta}2.59; {delta} 4.08 and {delta}1.67; O-(CH{sub 2}CH{sub 2}){sub n}-O from the PEG unit at {delta} 3.61. The molar composition of polyester copolymer was measured as the area ratio of {delta}3.61/({delta}4.08 + {delta}1.67) peak. The PEG unit is incorporated into the copolymers in an amount of about 9.12mol% less than that of the feed proportion. These results showed that the composition of the copolymers is in good agreement with that expected from the feed proportion. Highlights: Black-Right-Pointing-Pointer The introduction of PEG unit changed the flexibility of PBS main chain. Black-Right-Pointing-Pointer PEG unit did not alter the crystal form of PBS in copolymers. Black-Right-Pointing-Pointer PEG unit hindered the formation of ring-banded spherulite morphology in copolymers. Black-Right-Pointing-Pointer The copolyesters had good in vitro degradation performance. Black-Right-Pointing-Pointer The composition ratio of PEG unit can adjust the in vitro degradation performance.

  3. Synthesis and characterization of polyester copolymers based on poly(butylene succinate) and poly(ethylene glycol)

    International Nuclear Information System (INIS)

    A series of polyester copolymers was synthesized from 1,4-succinic acid with 1,4-butanediol and poly(ethylene glycol) through a two-step process of esterification and polycondensation in this article. The composition and physical properties of copolyesters were investigated via GPC, 1HNMR, DSC and PLM. The copolymer composition was in good agreement with that expected from the feed composition of the reactants. The melting temperature (Tm), crystallization temperature (Tc), and crystallinity (Xc) of these copolyesters decreased gradually as the content of PEG unit increased. Otherwise, experimental results also showed that the contents of PEG in copolymers had an effect on the molecular weight, distribution, thermal properties, hydrolysis degradation properties, and crystalline morphology of polyester copolymers. - Graphical abstract: The composition of polyester copolymer was determined from the 1H NMR spectra using the relative intensities of the proton peaks. As a sample, the 1H NMR spectrum of polyester copolymer with 10 mol% of PEG is shown in Fig. 2: CO-(CH2)2-CO; O-CH2- and C-(CH2)2-C from the SA and BD unit at δ2.59; δ 4.08 and δ1.67; O-(CH2CH2)n-O from the PEG unit at δ 3.61. The molar composition of polyester copolymer was measured as the area ratio of δ3.61/(δ4.08 + δ1.67) peak. The PEG unit is incorporated into the copolymers in an amount of about 9.12mol% less than that of the feed proportion. These results showed that the composition of the copolymers is in good agreement with that expected from the feed proportion. Highlights: ► The introduction of PEG unit changed the flexibility of PBS main chain. ► PEG unit did not alter the crystal form of PBS in copolymers. ► PEG unit hindered the formation of ring-banded spherulite morphology in copolymers. ► The copolyesters had good in vitro degradation performance. ► The composition ratio of PEG unit can adjust the in vitro degradation performance.

  4. Effect of uncoated calcium carbonate and stearic acid coated calcium carbonate on mechanical, thermal and structural properties of poly(butylene terephthalate) (PBT)/calcium carbonate composites

    Indian Academy of Sciences (India)

    G S Deshmukh; S U Pathak; D R Peshwe; J D Ekhe

    2010-06-01

    PBT/CaCO3 composites were prepared in a single screw extruder with particle content varying from 0–30% by weight. The influence of surface treatment of the particles, with and without stearic acid (SA), on the mechanical, thermal and structural properties was studied. The experiments included tensile tests, impact tests, differential scanning calorimetry (DSC), scanning electron microscopy (SEM), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy. The composite systems containing SA coated CaCO3 were found to exhibit better mechanical properties as compared to composite systems containing uncoated CaCO3, with the S3 system (20% of SA coated CaCO3) exhibiting best combination of mechanical properties. Thermal study revealed that particle type and content had no influence on the melting temperature but the crystallization temperature, % crystallinity and thermal stability increased on increasing the CaCO3 content in PBT matrix. Morphological observation indicated that in PBT composites containing SA coated CaCO3, the coupling agent favours a better polymer filler interaction rendering inorganic polymer interface compatible, which is also evident from better mechanical and thermal properties.

  5. Biodegradability of Poly (Butylene Succinate)%聚丁二酸丁二醇酯生物降解性能研究

    Institute of Scientific and Technical Information of China (English)

    孙炳新; 揣成智; 韩春阳; 罗思; 郭迎

    2014-01-01

    目的 研究酶解与水解对聚丁二酸丁二醇酯(PBS)生物降解性能的影响.方法 将PBS薄膜分别置于酶液与磷酸缓冲液中进行酶解与水解试验,利用热失重分析(TG)、X射线衍射(X-RD)、扫描电镜(SEM)以及失重率等测试手段或指标,对材料的生物降解性能进行表征.结果 TG与X-RD的测试结果表明,酶解后材料的热稳定性下降,热分解温度由308.83℃降低到282.85℃,同时材料的结晶度呈现一定程度的下降.水解后材料的热稳定性呈现出先降低再升高的趋势,而结晶度则基本维持不变.SEM与失重率结果证实,PBS的酶解主要通过表面侵蚀的方式进行,材料的失重率呈线性增长的趋势,降解10周后失重率约为33.2%;而水解则主要以整体侵蚀的方式进行,材料的失重率变化并不明显,降解20周后失重率仅为4.7%.结论 PBS的酶解与水解是2个截然不同的过程,酶解是表面侵蚀,而水解则是整体侵蚀.

  6. Effect of Hydroxyapatite Nanoparticles on the Degradability of Random Poly(butylene terephthalate-co-aliphatic dicarboxylates Having a High Content of Terephthalic Units

    Directory of Open Access Journals (Sweden)

    Nina Heidarzadeh

    2016-07-01

    Full Text Available Copolyesters derived from 1,4-butanediol and constituted also of aliphatic and aromatic dicarboxylate units in a molar ratio of 3:7 were synthesized by a two-step polycondensation procedure. Succinic, adipic, and sebacic acids were specifically selected as the aliphatic component whereas terephthalic acid was chosen as the aromatic moiety. The second synthesis step was a thermal transesterification between the corresponding homopolymers, always attaining a random distribution as verified by NMR spectroscopy. Hybrid polymer composites containing 2.5 wt % of hydroxyapatite (HAp were also prepared by in situ polymerization. Hydroxyl groups on the nanoparticle surface allowed the grafting of polymer chains in such a way that composites were mostly insoluble in the typical solvents of the parent copolyesters. HAp had some influence on crystallization from the melt, thermal stability, and mechanical properties. HAp also improved the biocompatibility of samples due to the presence of Ca2+ cations and the damping effect of phosphate groups. Interestingly, HAp resulted in a significant increase in the hydrophilicity of samples, which considerably affected both enzymatic and hydrolytic degradability. Slight differences were also found in the function of the dicarboxylic component, as the lowest degradation rates was found for the sample constituted of the most hydrophobic sebacic acid units.

  7. Performance comparison of poly(butylene succinate)modified by PTA and CHDM%PTA和CHDM改性聚丁二酸丁二醇酯的性能比较研究

    Institute of Scientific and Technical Information of China (English)

    张敏; 赵研; 惠媛媛; 张若琳; 邱建辉

    2012-01-01

    将含有苯环的对苯二甲酸(PTA)和六元环的1,4-环己烷二甲醇(1,4-CHDM)引入PBS分子主链中,得到PBS-co-PTA和PBS-co-CHDM的无规共聚物.1H-NMR鉴定了共聚物为预期产物,并对共聚物的热性能、结晶性和力学性能进行了对比研究.结果表明:PTA和1,4-CHDM改性后共聚物的结晶度变化截然不同,随着PTA含量的增加,PBS-co-PTA的结晶度、结晶尺寸逐渐增大,同时Tg逐渐降低;而随1,4-CHDM含量的增加,PBS-co-CHDM的结晶度和结晶尺寸却减小,Tg逐渐上升.当1,4-CHDM增至30%时,其断裂伸长率可达到PBS的3倍,证明了共聚物PBS-co-CHDM比PBS-co-PTA具有更好的柔韧性.%PBS-co-PTA and PBS-co-CHDM random copolymers are obtained, taking tereph-thalic acid (PTA) containing benzene ring and 1, 4-Cyclohexanedimethanol (1,4-CHDM) with six- membered ring into PBS main chain. The product copolymers are identified to be expected by ]HNMR, and molecular weight, thermal properties, mechanical performance and degradations of them are also compared. The results show that PTA and 1,4-CHDM modified copolymers present different crystallinities; with increasing contents of PTA, crys-tallinity and crystal size of PBS-co-PTA increase, while Tg gradually reduces; and along with the increase of 1,4-CHDM, crystallinity and crystal size of PBS-co-CHDM decrease, but Te gradually increases. When the content of 1,4-CHDM is to 30%, the elongation at break of PBS-co-CHDM is three times that of PBS, which proves PBS-co-CHDM has better flexibility than PBS-co-PTA.

  8. Synthesis and Characterization of Biodegradable Poly(butylene succinate-co-diethylene succinate)%生物降解聚丁二酸丁二醇/二甘醇酯的合成与性能研究

    Institute of Scientific and Technical Information of China (English)

    肖峰; 王庭慰; 丁培; 包艳华; 王景春

    2011-01-01

    以丁二酸(SA)、1,4-丁二醇(BD)和二甘醇(DEG)为原料,通过直接聚合法合成了可生物降解的聚丁二酸丁二醇/二甘醇酯(PBDGS).采用 1H-NMR,GPC,DSC等对产物进行了表征,研究了物料配比对共聚酯热性能、力学性能、降解性能和亲水性的影响.结果表明,DEG的引入能够有效抑制聚酯链段的结晶能力,同时改善材料的亲水性,使其降解性能较纯PBS有显著提高.

  9. Feasibility study of naphthalene removal: Naphthalene solubilization in aqueous solutions of a triblock copolymer of ethylene oxide and 1,2-butylene oxide, E64B20E64

    OpenAIRE

    Colin Booth; Proespichaya Kanatharana; Chiraphon Chaibundit

    2003-01-01

    Block copolymer E64B20E64, where E denotes oxyethylene, OCH2CH2, B denotes oxybutylene, OCH2CH (C2H5), and the subscripts denote number-average block lengths in repeat units, was synthesized by sequential anionic polymerization. Characterization was by gel permeation chromatography (for molar mass distribution) and 13C-NMR spectroscopy (for absolute molar mass and conformation of block architecture). Dynamic and static light scattering were used to study micellization and micelle properties o...

  10. Feasibility study of naphthalene removal: Naphthalene solubilization in aqueous solutions of a triblock copolymer of ethylene oxide and 1,2-butylene oxide, E64B20E64

    Directory of Open Access Journals (Sweden)

    Colin Booth

    2003-11-01

    Full Text Available Block copolymer E64B20E64, where E denotes oxyethylene, OCH2CH2, B denotes oxybutylene, OCH2CH (C2H5, and the subscripts denote number-average block lengths in repeat units, was synthesized by sequential anionic polymerization. Characterization was by gel permeation chromatography (for molar mass distribution and 13C-NMR spectroscopy (for absolute molar mass and conformation of block architecture. Dynamic and static light scattering were used to study micellization and micelle properties of this copolymer in dilute aqueous solution and in the presence of naphthalene. Dynamic light scattering was used to analyze hydrodynamic radius, rh and hydrodynamic expansion factor, δh. Static light scattering was used to study micelle association number, Nw, thermodynamic expansion factor, δt, and thermodynamic radius, rt. The presence of naphthalene in micellar core increased Nw by 50% and increased micellar size.

  11. 改性淀粉纳米晶对聚丁二酸丁二醇酯的增强改性研究%Study on Reinforcing of Poly(Butylene Succinate)by Modified Starch Nanocrystals

    Institute of Scientific and Technical Information of China (English)

    高山俊; 尹凯凯

    2011-01-01

    通过2,4-甲苯二异氰酸酯(TDl)与淀粉纳米晶(NST)在有机溶剂中的接枝反应制备了TDI改性淀粉纳米晶(NTST),然后将其与聚丁二酸丁二醇酯(PBS)熔融共混制备了PBS/NTST复合材料.改性淀粉纳米晶的红外光谱分析、X-射线衍射分析、润湿性实验和接触角测试结果表明,接枝反应成功进行,改性后的淀粉纳米粒子具有亲油性、低表面能的特点.复合材料的红外光谱分析、力学性能测试、热性能分析和扫描电镜测试结果表明,改性淀粉纳米晶均匀分散在PBS基体中,复合材料的力学性能和热性能均得到提高.%The modified starch nanocrystals(NTST) were prepared by the grafting reaction of toluene 2,4diisocyanate(TDI) and starch nanocrystals in organic solvents, then NTST were used as fillers to prepare PBS/ NTST nanocomposites by melt blending. NTST was characterized by infrared spectroscopy analysis, X-ray diffraction analysis, wettability tests and contact angle measurements. The results showed that the grafting reaction of TDI and starch nanocrystals was successful and NTST was hydrophobic with low surface energy. The PBS/NTST nanocomposites were characterized by FTIR, differential thermal analysis (DTA), tensile tests and scanning electron microscopy. The results showed that NTST dispersed uniformly in the PBS matrix and the obtained nanocomposites were increased in thermal stability and in strength.

  12. 单宁与聚磷酸铵复配体系对聚丁二酸丁二酯的催化成炭作用%Catalytic Charring Effect of Tannin and Ammonium Polyphosphate on Poly(Butylene Succinate)

    Institute of Scientific and Technical Information of China (English)

    冉诗雅; 陈超; 徐灵钢; 郭正虹

    2014-01-01

    采用热失重分析仪、微型量热仪及扫描电镜研究了单宁(Tannin)与聚磷酸铵(APP)复配体系对聚丁二酸丁二酯(PBS)的催化成炭作用以及炭层对其燃烧行为的影响.热失重分析表明,无论在空气还是氮气下,APP与Tannin复配使用都可以催化PBS体系成炭.当APP与Tannin的质量比为3∶1时,在空气中PBS体系700℃时残炭的实验值为9.3%,在氮气中残炭的实验值为11.3%,都远远高于理论计算值.微型量热仪分析显示,炭层可以作为基体与火焰之间的屏障,尤其当APP与Tannin的比例为5∶1时,PHRR降低了33%.此外,残炭形貌分析表明,APP和Tannin复配使用后,材料表面形成较为均匀、致密的炭层结构.

  13. Evaluation on the effect of the poly (butylenes succinate) biodegradation process on plant growth%聚丁二酸丁二醇酯(PBS)生物降解过程对植物生长的影响评价

    Institute of Scientific and Technical Information of China (English)

    李成涛; 张敏; 欧阳亮; 刘俊玲; 苏康宇; 邱建辉

    2011-01-01

    通过苏丹草(Sorghum sudanense Stapf)、籽粒笕(Amaranthus hypochondriacus L.)、豇豆(Vigna sesquipedalis Wight)种子的发芽试验及其盆栽试验,考察了PBS在土壤浸提液中的生物降解性能,探讨了PBS高聚物、低聚物和合成单体对植物的发芽和生长影响.研究结果表明:①在土壤浸提液中微生物对PBS有一定的降解作用,且在降解过程中,降解液的pH变化不明显;②PBS高聚物的降解产物对植物生长没有影响;③PBS低聚物在降解初期抑制部分植物的幼苗生长,后期对植物的生长没有影响;④当丁二酸的质量浓度低于200 mg·L-1时,对植物种子的发芽和幼苗生长不会产生影响,当质量浓度高于500mg·L-1时,将抑制幼苗生长;当1,4-丁二醇的质量浓度低于2 000mg·L-1时,对种子的发芽和生长没有影响.%In this paper, we have do experiment of the seed germination and plant growth such as Sudan grass, Purple grainjian and cowpea to investigate the degradation of PBS in the soil extract liquid, discuss the effect of polymers, oligomers and monomers of PBS on the germination and growth of plants. The results show that: ①Microorganisms in the soil extract liquid can degrade PBS and the pH of the degradation liquid did not change significantly. ②The degradation progress of polymer has no effect on the plant growth. ③The degradation products of PBS oligomers inhibit the growth of some seedlings in initial stages, but have no effect in later stage. ④When the succinate concentration is lower than 200 mg·L-1, it has no effect to the plant seed germination and seedling growth, but when it is higher than 500 mg·L-1, it will inhibit the seedling growth. When the 1, 4 - butanediol concentration is less than 2 000 mg·L-1, it has no effect to the seed germination and growth.

  14. An Efficient Catalyst for the Direct Synthesis of N-Phenylpyrrolidine

    Institute of Scientific and Technical Information of China (English)

    Chun Mei LI; Zhi Li MIAO; Lei SHI; Qi SUN; Yu Hong HE

    2006-01-01

    N-Phenylpyrrolidine was efficiently synthesized over the mesoporous Al2O3 catalyst by the reaction of the aniline and 1,4-butylene-glycol at atmospheric pressure. The catalyst exhibited very high activity and selectivity. At the reaction temperature of 300℃, 1,4-butylene glycol conversion attained 100% and the selectivity of N-phenylpyrrolidine could exceed 98%.

  15. Microbial degradation of aliphatic and aliphatic-aromatic co-polyesters.

    Science.gov (United States)

    Shah, Aamer Ali; Kato, Satoshi; Shintani, Noboru; Kamini, Numbi Ramudu; Nakajima-Kambe, Toshiaki

    2014-04-01

    Biodegradable plastics (BPs) have attracted much attention since more than a decade because they can easily be degraded by microorganisms in the environment. The development of aliphatic-aromatic co-polyesters has combined excellent mechanical properties with biodegradability and an ideal replacement for the conventional nondegradable thermoplastics. The microorganisms degrading these polyesters are widely distributed in various environments. Although various aliphatic, aromatic, and aliphatic-aromatic co-polyester-degrading microorganisms and their enzymes have been studied and characterized, there are still many groups of microorganisms and enzymes with varying properties awaiting various applications. In this review, we have reported some new microorganisms and their enzymes which could degrade various aliphatic, aromatic, as well as aliphatic-aromatic co-polyesters like poly(butylene succinate) (PBS), poly(butylene succinate)-co-(butylene adipate) (PBSA), poly(ε-caprolactone) (PCL), poly(ethylene succinate) (PES), poly(L-lactic acid) (PLA), poly(3-hydroxybutyrate) and poly(3-hydoxybutyrate-co-3-hydroxyvalterate) (PHB/PHBV), poly(ethylene terephthalate) (PET), poly(butylene terephthalate) (PBT), poly(butylene adipate-co-terephthalate (PBAT), poly(butylene succinate-co-terephthalate) (PBST), and poly(butylene succinate/terephthalate/isophthalate)-co-(lactate) (PBSTIL). The mechanism of degradation of aliphatic as well as aliphatic-aromatic co-polyesters has also been discussed. The degradation ability of microorganisms against various polyesters might be useful for the treatment and recycling of biodegradable wastes or bioremediation of the polyester-contaminated environments. PMID:24522729

  16. Morphology and properties of PBT/SEBS and PBT/SEBS-G-MAH blends

    Science.gov (United States)

    Lu, Xiang; Qu, Jinping

    2016-03-01

    A series of poly (butylene terephthlate) (PBT)/ styrene-ethylene/butylene-styrene (SEBS) and PBT/ (styrene-ethylene/butylene-styrene)-G-(Maleic anhydride) (SEBS-G-MAH) blends were prepared by melt blending method. And the morphology, mechanical properties were studied to identify the effect of SEBS or SEBS-G-MAH weight fraction on the properties of blends. SEM show that the minor phase was hardly distinguishable in the blend of PBT/SEBS-G-MAH as the result of the improvement in dispersibility, compared with PBT/SEBS blends. These results lead to the different mechanical properties between PBT/SEBS and PBT/SEBS-G-MAH blends.

  17. Preparation, Mechanical, and Thermal Properties of Biodegradable Polyesters/Poly(Lactic Acid Blends

    Directory of Open Access Journals (Sweden)

    Peng Zhao

    2010-01-01

    Full Text Available Series of biodegradable polyesters poly(butylene adipate (PBA, poly(butylene succinate (PBS, and poly(butylene adipate-co-butylene terephthalate (PBAT were synthesized successfully by melt polycondensation. The polyesters were characterized by Fourier transform infrared spectroscopy (FTIR, 1H-NMR, differential scanning calorimetry (DSC, and gel permeation chromatography (GPC, respectively. The blends of poly(lactic acid (PLA and biodegradable polyester were prepared using a twin screw extruder. PBAT, PBS, or PBA can be homogenously dispersed in PLA matrix at a low content (5–20 wt%, yielding the blends with much higher elongation at break than homo-PLA. DSC analysis shows that the isothermal and nonisothermal crystallizabilities of PLA component are promoted in the presence of a small amount of PBAT.

  18. Metal cleaner poisoning

    Science.gov (United States)

    Metal cleaners are very strong chemical products that contain acids. This article discusses poisoning from swallowing or ... Metal cleaners contain organic compounds called hydrocarbons, including: 1,2-butylene oxide Boric acid Cocoyl sarcosine Dicarboxylic ...

  19. Estudio del comportamiento mecánico de gelés físicos termorreversibles obtenidos a partir de copolímeros tribloques de PS-b-poli(etileno/butileno)-PS en un disolvente selectivo del bloque central

    OpenAIRE

    Hernáez, E.; Inchausti, I; Quintana, J. R.; Katime, I.

    2001-01-01

    The thermoreversible gelation of three triblock copolymers polystyrene-bpoly( ethylene/butylene)-b-polystyrene, with different molar mass and a similar chemical composition, in n-octane was studied. The solvent is selective for the middle poly(ethylene/butylene) block of the copolymers. The influence of the molar mass of the three copolymers on the gelation and on the mechanical properties of the gels was analysed. The sol-gel transition temperatures, Tgel, have been de...

  20. Hydroxyapatite reinforced chitosan and polyester blends for biomedical applications

    OpenAIRE

    Correlo, V.M.; Boesel, L. F.; Bhattacharya, Mrinal; Mano, J. F.; Neves, N. M.; Reis, R. L.

    2005-01-01

    Hydroxyapatite, chitosan, and aliphatic polyester were compounded using a twin-screw extruder. The polyesters include poly(e-caprolactone) (PCL), poly(lactic acid) , poly(butylene succinate) (PBS), and poly(butylene terephthalate adipate). The mass fraction of chitosan ranged from 17.5 to 45%, while that of HA ranged from 10 to 30%. These blends were injection molded and evaluated for thermal, morphological, and mechanical properties. The addition of hydroxyapatite dec...

  1. Analise térmica e microscópica de laminados biodegradáveis obtidos a partir de farinha de mandioca, sorbitol e poli (butileno adipato co-tereftalato PBAT. Thermal and microscopic analysis of biodegradable laminates made from cassava flour, sorbitol and poly (butylene adipate-co-terephthalate PBAT - doi: 10.4025/actascitechnol.v35i4.13183

    Directory of Open Access Journals (Sweden)

    Henrique Tirolli Rett

    2013-10-01

    Full Text Available O objetivo deste trabalho foi desenvolver blendas de materiais laminados biodegradáveis, utilizando farinha de mandioca como fonte de amido, fibras naturais, sorbitol como plastificante e PBAT. Primeiro obteve-se peletes de três formulações diferentes e a partir destes, utilizou-se a termoprensagem a alta temperatura como alternativa na formação dos laminados. A caracterização foi feita através de microscopia eletrônica de varredura (MEV e calorimetria diferencia de varredura (CDV. A quantidade se sorbitol que melhor se ajustou à extrusão foi a de 15% (peso/peso; a formulação do laminado mais homogêneo, observada pela microscopia, foi de 55:40:15 (farinha/sorbitol/PBAT. As fibras ficaram dispersas por toda a superfície nos três tratamentos estudados, porém, por dentre eles, observaram-se zonas dispersas das fibras. Conforme se aumentou o teor de farinha, houve aumento no ponto de fusão dos laminados em comparação ao PBAT puro.Blends of biodegradable laminated materials were developed using cassava flour as starch and natural fibers source, sorbitol as a plasticizer and PBAT as a biodegradable polyester. After obtaining pellets from three different formulations, high temperature thermopressure was used to form laminates. The characterization was performed by scanning electron microscopy (SEM and by differential scanning calorimetry (DSC. The amount of sorbitol for the best extrusion process was 15% (weight/weight and the formulation of the best homogeneity observed by microscopy was 55:40:15 (flour/sorbitol/PBAT. Although fibers were dispersed throughout the surface in the three treatments, scattered areas of fibers could be found among them. As rates of flour increased, an increase in the melting point of the laminates occurred when compared to pure PBAT.  

  2. 嵌段聚合物聚乳酸-聚丁二酸丁二醇酯-聚乳酸的制备及其性能研究%Study on the Properties of Block Copolymer Polylactide-poly(butylene succinate)-polylactide and Its Preparation

    Institute of Scientific and Technical Information of China (English)

    段久芳; 郭宝华

    2009-01-01

    采用熔融聚合法以聚丁二酸丁二醇膏(PBS)引发外消旋丙交酯(D,L-LA)成功制备了嵌段聚合物聚乳酸-聚丁二酸丁二醇酯-聚乳酸(PBSLA),采用核磁共振、DSC和偏光显微镜(POM)对聚合物的结构进行了表征.结果表明:外消旋聚乳酸(PDLA)嵌段部分的引入影响PBS分子链的规整排列,嵌段聚合物不再形成规整球晶,结晶度为41.5%,Tm为98.7℃.

  3. Biomineralization of Engineered Spider Silk Protein-Based Composite Materials for Bone Tissue Engineering

    Directory of Open Access Journals (Sweden)

    John G. Hardy

    2016-07-01

    Full Text Available Materials based on biodegradable polyesters, such as poly(butylene terephthalate (PBT or poly(butylene terephthalate-co-poly(alkylene glycol terephthalate (PBTAT, have potential application as pro-regenerative scaffolds for bone tissue engineering. Herein, the preparation of films composed of PBT or PBTAT and an engineered spider silk protein, (eADF4(C16, that displays multiple carboxylic acid moieties capable of binding calcium ions and facilitating their biomineralization with calcium carbonate or calcium phosphate is reported. Human mesenchymal stem cells cultured on films mineralized with calcium phosphate show enhanced levels of alkaline phosphatase activity suggesting that such composites have potential use for bone tissue engineering.

  4. Advances in Application of New Catalytic Materials in Petroleum Refining and Petrochemicals Production

    Institute of Scientific and Technical Information of China (English)

    He Yigong; Lin Min; Mu Xuhong; Shu Xingtian

    2006-01-01

    This article introduces the solid acid catalyst for isobutene/butylenes alkylation, the HTS Ti/Si zeolite for ammonoxidation of cyclohexanone and the noncrystalline alloy catalyst and magnetically stabilized bed for hydrofining of caprolactam that were developed recently by SINOPEC Research Institute of Petroleum Processing (RIPP).

  5. Biodegradable composites from polyester and sugar beet pulp with antimicrobial coating for food packaging

    Science.gov (United States)

    Totally biodegradable, double-layered antimicrobial composite Sheets were introduced for food packaging. The substrate layers of the sheets were prepared from poly (lactic acid) (PLA) and sugar beet pulp (SBP) or poly (butylene adipate-co-terephthalate (PBAT) and SBP by a twin-screw extruder. The ac...

  6. Gas plasma etching of PEO/PBT segmented block copolymer films

    NARCIS (Netherlands)

    Olde Riekerink, M.B.; Claase, M.B.; Engbers, G.H.M.; Grijpma, D.W.; Feijen, J.

    2003-01-01

    A series of poly(ethylene oxide)/poly(butylene terephthalate) (PEO/PBT) segmented block copolymer films was treated with a radio-frequency carbon dioxide (CO2) or with argon (Ar) plasma. The effects of (preferential) etching on surface structure, topography, chemistry, and wettability were studied b

  7. Polypropylene/organoclay/SEBS nanocomposites with toughness-stiffness properties

    DEFF Research Database (Denmark)

    Sanporean (nee Potarniche), Catalina-Gabriela; Vuluga, Zina; Radovici, Constantin;

    2014-01-01

    Polypropylene nanocomposites with a different amount of styrene-ethylene-butylene-styrene block copolymer (SEBS)/clay were prepared via a melt mixing technique. To improve the dispersion of commercial organoclay (denoted as OMMT), various amounts of SEBS were incorporated. At a fixed content of O...

  8. Are reactive thermoplastic polymers suitable for future wind turbine composite materials blades?

    DEFF Research Database (Denmark)

    Raghavalu Thirumalai, Durai Prabhakaran

    2014-01-01

    , it was found that only two potential reactive thermoplastic resin systems qualify for different processing requirements for blade manufacturing. Hence, the article focuses on the issues with the use of reactive polymers like APA-6 (Caprolactam) and CBT (Cyclic Butylene Terephtalate) resin systems for composite...

  9. CO2-selective PEO–PBT (PolyActive™)/graphene oxide composite membranes

    KAUST Repository

    Karunakaran, M.

    2015-07-31

    CO2-selective graphene oxide (GO) nano-composite membranes were prepared for the first time by embedding GO into a commercially available poly(ethylene oxide)–poly(butylene terephthalate) (PEO–PBT) copolymer (PolyActive™). The as-prepared GO membrane shows high CO2 permeability (143 Barrer) and CO2/N2 selectivity (α = 73).

  10. PEOT/PBT based scaffolds with low mechanical properties improve cartilage repair tissue formation in osteochondral defects

    NARCIS (Netherlands)

    Jansen, Edwin J. P.; Pieper, Jeroen; Gijbels, Marion J. J.; Guldemond, Nick A.; Riesle, Jens; Van Rhijn, Lodewijk W.; Bulstra, Sjoerd K.; Kuijer, Roel

    2009-01-01

    The aim of our Study was to compare the healing response of biomechanically and biochemically different scaffolds in osteochondral defects created in rabbit medial femoral condyles. A block copolymer comprised of poly(ethylene oxide terephthalate) and poly(butylene terephthalate) was used to prepare

  11. Direct production of lower olefins from synthesis gas using supported iron catalysts

    NARCIS (Netherlands)

    Torres Galvis, H.M.

    2013-01-01

    Lower olefins (ethylene, propylene and butylenes) are important commodity chemicals used for the manufacture of, amongst others, plastics, solvents and lubricants to cosmetics and drugs. C2 to C4 olefins are conventionally produced by steam cracking of naphtha. In view of economic, strategic, and en

  12. Isolation and characterization of a bacterium that degrades various polyester-based biodegradable plastics.

    Science.gov (United States)

    Teeraphatpornchai, T; Nakajima-Kambe, T; Shigeno-Akutsu, Y; Nakayama, M; Nomura, N; Nakahara, T; Uchiyama, H

    2003-01-01

    Microorganisms isolated from soil samples were screened for their ability to degrade various biodegradable polyester-based plastics. The most active strain, designated as strain TB-13, was selected as the best strain for degrading these plastics. From its phenotypic and genetic characteristics, strain TB-13 was closely related to Paenibacillus amyloyticus. It could degrade poly(lactic acid), poly(butylene succinate), poly(butylene succinate-co-adipate), poly(caprolactone) and poly(ethylene succinate) but not poly(hydroxybutylate-co-valerate). However, it could not utilize these plastics as sole carbon sources. Both protease and esterase activities, which may be involved in the degradation of plastic, were constitutively detected in the culture broth. PMID:12882301

  13. A calibration test for latent fingerprint development on thermal paper.

    Science.gov (United States)

    Spencer, Caroline A; Bond, John W

    2014-11-01

    A calibration test is described for monitoring the operation of equipment used to develop latent fingerprints on thermal paper by the application of either controlled or uncontrolled heat. A working solution of a water/glycerol emulsion and butylene glycol is applied to thermal paper by means of either a vinyl stamp and pad, or a marker pen. Varying the amount of butylene glycol enables the thermal paper to change color at different temperatures between approximately 40 and 60°C, which is below the normal color change temperature of the paper. The described test may be used to verify the correct operation, at different temperatures, of a controlled heat source during and after fingerprint development (such as the Hot Print System) or to monitor the paper temperature with an uncontrolled heat source (such as a warm air blower), thereby avoiding unintentional coloring of the entire paper surface.

  14. Direct production of lower olefins from synthesis gas using supported iron catalysts

    OpenAIRE

    Torres Galvis, H.M.

    2013-01-01

    Lower olefins (ethylene, propylene and butylenes) are important commodity chemicals used for the manufacture of, amongst others, plastics, solvents and lubricants to cosmetics and drugs. C2 to C4 olefins are conventionally produced by steam cracking of naphtha. In view of economic, strategic, and environmental reasons there is a growing necessity to produce these key chemical building blocks from non-oil derived sources. Many processes have been devised to obtain lower olefins from synthesis ...

  15. Conductivity of microfibrillar polymer-polymer composites with CNT-loaded microfibrils or compatibilizer: A comparative study

    OpenAIRE

    Fakirov, S.; S. M. Panamoottil; P. Potschke; R. J. T. Lin; Bhattacharyya, D

    2013-01-01

    Conductive polymer composites have wide ranging applications, but when they are produced by conventional melt blending, high conductive filler loadings are normally required, hindering their processability and reducing mechanical properties. In this study, two types of polymer-polymer composites were studied: i) microfibrillar composites (MFC) of polypropylene (PP) and 5 wt% carbon nanotube (CNT) loaded poly(butylene terephthalate) (PBT) as reinforcement, and ii) maleic anhydride-grafted poly...

  16. Development and Commercial Application of Methyl-ethyl-ketone Production Technology%甲乙酮成套技术开发及工业应用

    Institute of Scientific and Technical Information of China (English)

    刘振华; 霍稳周; 马皓; 乔凯

    2006-01-01

    A synthetic technology for the production of methyl-ethyl-ketone (MEK) is introduced, which makes use of butylene catalytic hydration to produce secondary butanol (SBA) and this is followed by dehydrogenation of SBA. By optimizing the operating conditions of a commercial unit, the running results showed that the recommended process was successful and that the catalysts had high activity, good selectivity, and long lifespan, which ensured long-term running in commercial units.

  17. Cyclic derivatives of D-glucose and tartaric acid as building blocks for renewable polyesters

    OpenAIRE

    Japu, Cristina

    2014-01-01

    Three series of aromatic copolyesters derived from poly(ethylene terephthalate) (PET), poly(butylene terephthalate) (PBT) and poly(hexamethylene terephthalate) (PHT) have been synthesized by melt polycondensation in which the terephthalate and oxyalkylene units have been partially or totally replaced by monocyclic and bicyclic diacids and diols obtained by derivatization of renewable monomers such as tartaric acid and D-glucose respectively. Another series of aliphatic copolyesters derived f...

  18. Mejora de la inercia térmica de mezclas de sebs mediante la adición de materiales con cambio de fase (PCMs) a 28 ºC

    OpenAIRE

    Juárez Varón, David; Ferrándiz Bou, Santiago; Fenollar Gimeno, Octavio Ángel; Fombuena Borrás, Vicent; Balart Gimeno, Rafael Antonio

    2012-01-01

    [EN] In this work, microencapsulated phase change materials (PCMs) with a melting temperature of 28 ºC have been used to improve thermal inertia phenomena on an elastomeric matrix of styrene-ethylene/butylenes-styrene (SEBS) material. The amount of PCMs has varied in the 1- 10 wt. % and these materials have been processed by conventional injection molding without PCM degradation. Mechanical characterization of SEBS-PCM compounds has been carried out and the obtained results...

  19. Développement de mélanges à base de polylactide à durée de vie contrôlée. Étude des relations microstructure / propriétés / mise en œuvre

    OpenAIRE

    Berthé, Vincente

    2010-01-01

    Co-encadrement de la thèse : Laurent Ferry et Jean-Charles Benezet This study is a part of a global research program aiming at developing innovative bio-composites based on biodegradable matrix (poly-lactide, poly-epsilon-caprolactone (PCL) and poly-butylen-succinate (PBS)) with controlled mechanical properties and life times in different weathering conditions. Besides, the blend end of life fragmentation are also studied. Different aspects of this global research program are developed in ...

  20. Novel Zn(II) ladder-like coordination polymer constructed from designed ferrocenyl ligand

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Reaction of Zn(NO3)2.6H2O with 3-(4-carboxylphenylamino)-1-ferrocenyl-2-butylen-1-one (HL) and 4,4'-bipyridine (4,4'-bipy) in methanol solution resulted in a novel ladder-like coordination polymer {[Zn2L2(μ2-L)2(4,4'-bipy)2].MeOH}n (1). Its crystal structure, thermal and electrochemical properties axe presented.

  1. Proton transport in proton exchange membranes

    OpenAIRE

    Schmeisser, Jennifer Mary

    2007-01-01

    This work investigated several proton exchange membranes (PEMs): perfluorosulfonic acid-based polymers (Nafion®), sulfonated poly(ether ether ketone) (S-PEEK), radiation-grafted ethylenetetrafluoroethylene-grafted-poly(styrene sulfonic) acid (ETFE-g-PSSA), sulfonated trifluorostyrene-co-substituted trifluorostyrene (BAM®), sulfonated polystyrene-b-poly(ethylene-r-butylene)-b-polystyrene triblock copolymer (S-SEBS), and a series of novel photocurable polyelectrolytes. These polymer systems dif...

  2. Significant Enhancement of Mechanical and Thermal Properties of Thermoplastic Polyester Elastomer by Polymer Blending and Nanoinclusion

    OpenAIRE

    Manwar Hussain; Young Hui Ko; Yong Ho Choa

    2016-01-01

    Thermoplastic elastomer composites and nanocomposites were fabricated via melt processing technique by blending thermoplastic elastomer (TPEE) with poly(butylene terephthalate) (PBT) thermoplastic and also by adding small amount of organo modified nanoclay and/or polytetrafluoroethylene (PTFE). We study the effect of polymer blending on the mechanical and thermal properties of TPEE blends with and without nanoparticle additions. Significant improvement was observed by blending only TPEE and v...

  3. Structure–property relationship of specialty elastomer–clay nanocomposites

    Indian Academy of Sciences (India)

    Anirban Ganguly; Madhuchhanda Maiti; Anil K Bhowmick

    2008-06-01

    The present work deals with the synthesis of specialty elastomer [fluoroelastomer and poly (styrene--ethylene-co-butylene--styrene (SEBS)]–clay nanocomposites and their structure–property relationship as elucidated from morphology studies by atomic force microscopy, transmission electron microscopy and X-ray diffraction and physico-mechanical properties. Due to polarity match, hydrophilic unmodified montmorillonite clay showed enhanced properties in resulting fluoroelastomer nanocomposites, while hydrophobic organo-clay showed best results in SEBS nanocomposites.

  4. 不同链结构的双酚A聚碳酸酯对脂肪族聚碳酸酯结晶行为的影响%EFFECT OF BISPHENOL A POLYCARBONATE WITH DIFFERENT CHAIN STRUCTURE ON THE CRYSTALLIZATION BEHAVIOR OF ALIPHATIC POLYCARBONATE

    Institute of Scientific and Technical Information of China (English)

    宁炜; 刘琛阳; 朱文祥; 李春成; 王笃金

    2012-01-01

    脂肪族聚碳酸酯(APC)是一类可降解的高分子材料,因其生产工艺可固定温室气体的主要成分二氧化碳,这种可降解塑料得到了越来越多的关注.作为半结晶高分子材料,脂肪族聚碳酸酯的结晶性能和结晶结构对成型加工、力学性能和降解性能具有重要的影响.借助热分析(示差扫描量热仪DSC)和形态学观察(偏光显微镜POM)两种方法研究了不同链结构的双酚A型聚碳酸酯对半结晶脂肪族聚碳酸酯——聚碳酸1,4-丁二醇酯结晶动力学行为的影响.实验发现质量分数1%的双酚A聚碳酸酯的加入促进了聚碳酸1,4-丁二醇酯的成核,但不同链结构的双酚A聚碳酸酯对其晶体生长具有相反的作用,线形双酚A聚碳酸酯(PC-L)能够促进晶体生长,而支化双酚A聚碳酸酯(PC-B)则抑制晶体生长.用原子力显微镜在轻敲模式下研究了两种双酚A聚碳酸酯与APC共混物熔融状态下的相结构,发现熔体结构的不同是导致两种共混物与纯的APC相比,结晶速率呈现相反变化趋势的主要原因.%In the present investigation, the effect of the chain structure and aggregation state of bisphenol A polycarbonate ( PC) on the crystallization kinetics and morphology of the poly ( butylene carbonate) has been studied by DSC and POM. It was found that the addition of bisphenol A polycarbonate A promoted the nucleation of the poly( butylene carbonate) , while the chain structure of PC had the opposite influence on the crystal growth rate of the poly ( butylene carbonate). The linear bisphenol A polycarbonate polycarbonate accelerates the crystal growth rate of poly ( butylene carbonate) , while the long chain-branched bisphenol A polycarbonate decelerates it. The phase images of the blends of aliphatic polycarbonates and bisphenol A polycarbonate were obtained under the tapping mode by atomic force microscopy ( AFM). The linear bisphenol A polycarbonate shows isolated irregular

  5. Synthesis of thermoplastic poly(ester-olefin elastomers

    Directory of Open Access Journals (Sweden)

    Tanasijević Branka

    2004-01-01

    Full Text Available A series of thermoplastic poly(ester-olefin elastomers, based on poly(ethylene-stat-butylene, HO-PEB-OH, as the soft segment and poly (butylene terephthalate, PBT, as the hard segment, were synthesized by a catalyzed transesterification reaction in solution. The incorporation of soft hydrogenated poly(butadiene segments into the copolyester backbone was accomplished by the polycondensation of α, ω-dihydroxyl telechelic HO-PEB-OH, (PEB Mn = 3092 g/mol with 1,4-butanediol (BD and dimethyl terephthalate (DMT in the presence of a 50 wt-% high boiling solvent i.e., 1,2,4-trichlorobenzene. The molar ratio of the starting comonomers was selected to result in a constant hard to soft weight ratio of 60:40. The synthesis was optimized in terms of both the concentration of catalyst, tetra-n-butyl-titanate (Ti(OBu4, and stabilizer, N,N'-diphenyl-p-phenylenediamine (DPPD, as well as the reaction time. It was found that the optimal catalyst concentration (Ti(OBu4 for the synthesis of these thermoplastic elastomers was 1.0 mmol/mol ester and the optimal DPPD concentration was 1.0 wt-%. The extent of the reaction was followed by measuring the inherent viscosity of the reaction mixture. The effectiveness of the incorporation of the soft segments into the copolymer chains was proved by Soxhlet extraction with chloroform. The molecular structures, composition and the size of the synthesized poly(ester-butylenes were verified by 1H NMR spectroscopy, viscometry of dilute solutions and the complex dynamic melt viscosity. The thermal properties of poly(ester-olefins were investigated by differential scanning calorimetry (DSC. The degree of crystallinity was also determined by DSC. The thermal and thermo-oxidative stability were investigated by thermogravimetric analysis (TGA. The rheological properties of poly(ester-olefins were investigated by dynamic mechanical spectroscopy in the melt and solid state.

  6. Atomistic modeling of bio-based polymeric fibers

    Science.gov (United States)

    Yeh, In-Chul; Rinderspacher, B. Christopher; Andzelm, Jan W.; Cureton, Lashonda T.; La Scala, John

    2013-03-01

    We performed molecular dynamics simulations on the amorphous phase of two bio-based polymers, poly (butylene furanamide) and poly (hexamethylene furanamide). Simulations of corresponding petroleum-based polymers, nylon 4, 6 and nylon 6, 6, were also performed. Glass transition temperatures estimated from a series of simulations were in good agreement with experimental measurements. Stress-strain relationships under uniaxial deformation were also analyzed. Bio-based polymers show higher glass transition temperatures and comparable yield points despite having overall weaker hydrogen bonds compared with their counterparts nylons. This result suggests that the furan ring plays an important role in the thermodynamic and mechanical properties of bio-based polymers.

  7. Environment-induced self-assembly in phase separated block copolymer systems: A SANS investigation

    International Nuclear Information System (INIS)

    In this research, we examine the effect of non-selective solvent on the large-scale mesoscopic ordering in asymmetric block copolymers, poly(styrene-block-ethylene/butylene-block-styrene) (SEBS) using small angle neutron scattering technique (SANS). SANS measurements were carried out over a wide range of concentrations and temperatures. Evolution of the self-assembled phase morphology in such polymer with the thermodynamic selectivity of solvent, temperature and concentration has been discussed. Correlation between morphology and thermorheological behavior of the gels has also been established

  8. Aesthetic laser marking assessment

    Science.gov (United States)

    Ng, T. W.; Yeo, S. C.

    2000-04-01

    In this paper, the CIE color difference formula was applied to evaluate four types of material surfaces; anodized aluminium, stainless steel, poly-butylene tetra-phthalate (PBT), and phenol formaldehyde, marked using a Nd:YAG laser, and viewed under three common modes of illumination; tungsten, fluorescent and daylight. The color difference values were based on the spectral reflectance readings obtained from a spectrophotometer. Each material exhibited different color difference trends in relation to marking speed for the different modes of illumination. Nevertheless, general comparisons could be made in terms of operational marking speeds and the maximal color difference values for each material.

  9. PROPERTIES OF POLYURETHANE ELASTOMERS BASED ON POLY (OXYETHYLENE-co-OXYTETRAMETHYLENE) DIOL

    Institute of Scientific and Technical Information of China (English)

    Chen-yu Su; Guang-li Zhang; Hong-zhi Zhang

    2001-01-01

    Polyurethane elastomers derived from 4,4′-methylene bis(phenyl isocyanate), butylene glycol and the low oxyethylene moiety content copolyether of tetrahydrofuran and ethylene oxide, obtained by copolymerization using heteropolyacid-ethylene oxide initiator system, were prepared. The polyurethanes exhibited an increased water absorption and much better low temperature resilience, which remained high even at a temperature of-3℃, while that of polyurethane based upon poly(tetramethylene ether) glycol of the same molecular weight, I.e. Being 2000, and molecular weight distribution, I.e. In the range of 1.4-1.5, starts to decrease dramatically at 5℃.``

  10. Allergic contact dermatitis to propyl gallate and pentylene glycol in an emollient cream.

    Science.gov (United States)

    Foti, Caterina; Bonamonte, Domenico; Cassano, Nicoletta; Conserva, Anna; Vena, Gino A

    2010-05-01

    A 62-year-old man, with a 20-year history of seborrhoeic dermatitis, presented with a worsening of his dermatitis. He had previously been demonstrated to be allergic to various topical corticosteroids, so he had been using an emollient cream (Sebclair), containing piroctone olamine and various anti-inflammatory substances, for 6 months, with good effect. Patch testing to the cream and its ingredients revealed positive reactions to both propyl gallate and pentylene glycol. A positive reaction to propylene glycol was also detected, whereas patch testing to butylene glycol was negative. Complete remission followed avoidance of the offending substances. PMID:20546226

  11. Enhanced propylene production in FCC by novel catalytic materials

    Energy Technology Data Exchange (ETDEWEB)

    Kelkar, C.P.; Harris, D.; Xu, M.; Fu, J. [BASF Catalyst LLC, Iselin, NJ (United States)

    2007-07-01

    Fluid catalytic cracking is expected to increasingly supply the additional incremental requirements for propylene. The most efficient route to increase propylene yield from an FCC unit is through the use of medium pore zeolites such as ZSM-5. ZSM-5 zeolite cracks near linear olefins in the gasoline range to LPG olefins such as propylene and butylenes. This paper will describe catalytic approaches to increase gasoline range olefins and the chemistry of ZSM-5 to crack those olefins. The paper will also describe novel catalytic materials designed to increase propylene. (orig.)

  12. Kinetics and Mechanism of Oxidation of Some Diols by Dihydroxydiperiodatoargentate(Ⅲ) in Alkaline Medium

    Institute of Scientific and Technical Information of China (English)

    SHAN, Jin-Huan; LI, Sheng-Min; HUO, Shu-Ying; SHEN, Shi-Gang; SUN, Han-Wen

    2006-01-01

    The kinetics of oxidation of ethylene glycol and 1,3-butylene glycol by dihydroxydiperiodatoargentate(Ⅲ) in alkaline medium have been studied by spectrophotometry in the range of 298.2-318.2 K. It is shown that the reaction was first order with respect to each reductant and Ag(Ⅲ), and kobs increased with an increase of [OH-]. A plausible mechanism of reaction involving a pre-equilibrium of adduct formation between complex and reductants was proposed, which could be applied to explain all experimental phenomena, and the activation parameters of the ratedetermining step have been also calculated.

  13. Study of the structure and the mechanical properties of dynamically cured PP/MAH-g-SEBS/epoxy blends

    Institute of Scientific and Technical Information of China (English)

    Xue Liang Jiang; Yin Xi Zhang

    2009-01-01

    A new method concerning with the simultaneous reinforcing and toughening of polypropylene (PP) was reported. Dynamical cure of the epoxy resin was successfully applied in the PP/maleic anhydride-grafted styrene--ethylene-butylene-styrene (SEBS) triblock copolymer, and the obtained blends named as dynamically cured PP/MAH-g-SEBS/epoxy blends. The stiffness and toughness of the blends are in a good balance, and MAH-g-SEBS was acted as not only an impact modifier but also a compatibilizer. The structure of the dynamically cured PP/MAH-g-SEBS/epoxy blends is the embedding of the epoxy particles by the MAH-gSEBS.

  14. Rheological characterization and mathematical modeling of a SEBS blend for industrial applications where nowadays liquid silicone rubber is used

    OpenAIRE

    Juárez Varón, David; Ferrándiz Bou, Santiago; Balart Gimeno, Rafael Antonio; Reig Pérez, Miguel Jorge; Peydro, M. A.

    2012-01-01

    SEBS (styrene-ethylene/butylene-styrene) is a hydrogenated SBS used as a compatibilizer of other thermoplastic or as a blend to improve the properties (mainly impact). There is very little information about SEBS's research, independent of other materials. This study focuses on a blend from the provider's SEBS extreme hardness (50% Shore-A 5 and 50% Shore-A 90) in order to analyze the miscibility of mixed materials from the storage of 2 references only. It has been used the thermoplastic e...

  15. Composites structures for bone tissue reconstruction

    Energy Technology Data Exchange (ETDEWEB)

    Neto, W.; Santos, João [Universidade Federal de São Carlos, Departament of Materials Engineering - Rd. Washington Luis, Km 235, 13565-905, São Carlos-SP (Brazil); Avérous, L.; Schlatter, G.; Bretas, Rosario, E-mail: bretas@ufscar.br [Université de Strasbourg, ECPM-LIPHT - 25 rue Becquerel, 67087, Strasbourg (France)

    2015-05-22

    The search for new biomaterials in the bone reconstitution field is growing continuously as humane life expectation and bone fractures increase. For this purpose, composite materials with biodegradable polymers and hydroxyapatite (HA) have been used. A composite material formed by a film, nanofibers and HA has been made. Both, the films and the non-woven mats of nanofibers were formed by nanocomposites made of butylene adipate-co-terephthalate (PBAT) and HA. The techniques used to produce the films and nanofibers were spin coating and electrospinning, respectively. The composite production and morphology were evaluated. The composite showed an adequate morphology and fibers size to be used as scaffold for cell growth.

  16. Process for the reduction of nitrogen oxides in an effluent

    Energy Technology Data Exchange (ETDEWEB)

    Epperly, W.R.; Sullivan, J.C.; Sprague, B.N.

    1989-07-04

    This patent describes a process for the reduction of the concentration of nitrogen oxides in the effluent from the combustion of a carbonaceous fuel. The process comprises introducing a treatment agent which comprises a composition selected from the group consisting of NH/sub 4/-lignosulfonate, calcium lignosulfonate, 2-furoic acid, 1,3 dioxolane, tetrahydrofuran, furfurylamine, furfurylalcohol, gluconic acid, citric acid, n-butyl acetate, 1,3 butylene glycol, methylal, tetrahydrofuryl alcohol, furan, fish oil, coumalic acid, furfuryl acetate, tetrahydrofuran 2,3,4,5-tetracarboxylic acid, tetrahydrofurylamine, furylacrylic acid, tetrahydropyran, 2,5-furandimethanol, mannitol, hexamethylenediamine, barbituric acid, acetic anhydride, oxalic acid, mucic acid and d-galactose.

  17. The influence of chemical composition of aliphatic-aromatic copolyesters on their properties

    Energy Technology Data Exchange (ETDEWEB)

    Wojtczak, Malgorzata; Galeski, Andrzej; Piorkowska, Ewa [Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz (Poland); Dutkiewicz, Slawomir [Institute of Biopolymers and Chemical Fibres, Marii Sklodowskiej-Curie 19/27, 90-570 Lodz (Poland)

    2014-05-15

    The chain microstructure and properties of a series of aliphatic-aromatic copolyesters in a range of compositions from 10 to 100% of aromatic components were studied by examining melting and crystallization behaviors, dynamic mechanical response, morphology, wide- (WAXS) and small-angle X-ray scattering (SAXS), and tensile deformation. Chain microstructure was analyzed by {sup 1}H NMR. The results indicate that most of copolyesters used in this study have essentially random distribution of comonomers. Copolyesters with more than 30 mol% of aromatic part crystallize with a crystal structure characteristic for homopolymer poly(butylene terephthalate) (PBT). However, some of the reflections from crystal planes are shifted towards lower diffraction angles as compared to butylene terephthalate homoplymer. The phase transition temperatures decrease with increasing aliphatic content. By means of polarized light microscopy (PLM), small-angle light scattering (SALS) and SAXS, crystallization behavior of a selected aliphatic-aromatic copolyester was further explored. Selected copolyester crystallizes in the form of thin fibrous crystals, few nanometers thick, which is the main factor influencing the depression of its melting temperature.

  18. Simple replica micromolding of biocompatible styrenic elastomers.

    Science.gov (United States)

    Borysiak, Mark D; Bielawski, Kevin S; Sniadecki, Nathan J; Jenkel, Colin F; Vogt, Bryan D; Posner, Jonathan D

    2013-07-21

    In this work, we introduce a simple solvent-assisted micromolding technique for the fabrication of high-fidelity styrene-ethylene/butylene-styrene (SEBS) microfluidic devices with high polystyrene (PS) content (42 wt% PS, SEBS42). SEBS triblock copolymers are styrenic thermoplastic elastomers that exhibit both glassy thermoplastic and elastomeric properties resulting from their respective hard PS and rubbery ethylene/butylene segments. The PS fraction gives SEBS microdevices many of the appealing properties of pure PS devices, while the elastomeric properties simplify fabrication of the devices, similar to PDMS. SEBS42 devices have wettable, stable surfaces (both contact angle and zeta potential) that support cell attachment and proliferation consistent with tissue culture dish substrates, do not adsorb hydrophobic molecules, and have high bond strength to wide range of substrates (glass, PS, SEBS). Furthermore, SEBS42 devices are mechanically robust, thermally stable, as well as exhibit low auto-fluorescence and high transmissivity. We characterize SEBS42 surface properties by contact angle measurements, cell culture studies, zeta potential measurements, and the adsorption of hydrophobic molecules. The PS surface composition of SEBS microdevices cast on different substrates is determined by time-of-flight secondary ion mass spectrometry (ToF-SIMS). The attractive SEBS42 material properties, coupled with the simple fabrication method, make SEBS42 a quality substrate for microfluidic applications where the properties of PS are desired but the ease of PDMS micromolding is favoured. PMID:23670166

  19. Affinity purification and characterization of a biodegradable plastic-degrading enzyme from a yeast isolated from the larval midgut of a stag beetle, Aegus laevicollis.

    Science.gov (United States)

    Suzuki, Ken; Sakamoto, Hironori; Shinozaki, Yukiko; Tabata, Jun; Watanabe, Takashi; Mochizuki, Atsushi; Koitabashi, Motoo; Fujii, Takeshi; Tsushima, Seiya; Kitamoto, Hiroko K

    2013-09-01

    Two yeast strains, which have the ability to degrade biodegradable plastic films, were isolated from the larval midgut of a stag beetle, Aegus laevicollis. Both of them are most closely related to Cryptococcus magnus and could degrade biodegradable plastic (BP) films made of poly(butylene succinate) (PBS) and poly(butylene succinate-co-adipate) (PBSA) effectively. A BP-degrading enzyme was purified from the culture broth of one of the isolated strains employing a newly developed affinity purification method based on the binding action of the enzyme to the substrate (emulsified PBSA) and its subsequent degradative action toward the substrate. Partial amino acid sequences of this enzyme suggested that it belongs to the cutinase family, and thus, the enzyme was named CmCut1. It has a molecular mass of 21 kDa and a degradative activity for emulsified PBSA which was significantly enhanced by the simultaneous presence of Ca(2+) or Mg(2+) at a concentration of about 2.5 mM. Its optimal pH was 7.5, and the optimal temperature was 40 °C. It showed a broad substrate specificity for p-nitrophenyl (pNP)-fatty acid esters ranging from pNP-acetate (C2) to pNP-stearate (C18) and films of PBSA, PBS, poly(ε-caprolactone), and poly(lactic acid). PMID:23224497

  20. Phyllosphere yeasts rapidly break down biodegradable plastics.

    Science.gov (United States)

    Kitamoto, Hiroko K; Shinozaki, Yukiko; Cao, Xiao-Hong; Morita, Tomotake; Konishi, Masaaki; Tago, Kanako; Kajiwara, Hideyuki; Koitabashi, Motoo; Yoshida, Shigenobu; Watanabe, Takashi; Sameshima-Yamashita, Yuka; Nakajima-Kambe, Toshiaki; Tsushima, Seiya

    2011-01-01

    The use of biodegradable plastics can reduce the accumulation of environmentally persistent plastic wastes. The rate of degradation of biodegradable plastics depends on environmental conditions and is highly variable. Techniques for achieving more consistent degradation are needed. However, only a few microorganisms involved in the degradation process have been isolated so far from the environment. Here, we show that Pseudozyma spp. yeasts, which are common in the phyllosphere and are easily isolated from plant surfaces, displayed strong degradation activity on films made from poly-butylene succinate or poly-butylene succinate-co-adipate. Strains of P. antarctica isolated from leaves and husks of paddy rice displayed strong degradation activity on these films at 30°C. The type strain, P. antarctica JCM 10317, and Pseudozyma spp. strains from phyllosphere secreted a biodegradable plastic-degrading enzyme with a molecular mass of about 22 kDa. Reliable source of biodegradable plastic-degrading microorganisms are now in our hands. PMID:22126328

  1. Effects of Thermal and Solvent Aging on Breakdown Voltage of TPE, PBT/PET Alloy, and PBT Insulated Low Voltage Electric Wire

    Directory of Open Access Journals (Sweden)

    Eun-Soo Park

    2013-01-01

    Full Text Available Tests were performed to evaluate the effects of thermal and solvent aging on the mechanical and dielectric breakdown properties of four types of polyester resins, namely, the insulation layer of poly(butylene terephthalat (PBT- based thermoplastic elastomer (TPE, TPE1, poly(butylene 2,6-naphthalate-based TPE (TPE2, PBT/poly(ethylene terephthalate alloy (Alloy, and PBT extruded onto a copper conductor of low voltage electric wire. The tensile specimens used in this series were prepared from the same extruded resins. The prepared electric wires and tensile specimens were thermally aged in air and in toluene, xylene, TCB, and NMP. When Alloy and PBT were thermally aged in toluene, xylene and TCB at 120°C for 6 h, the tensile properties were significantly decreased compared to TPE1 and TPE2 at the same condition. The reduction of elongation at break of Alloy was more discernible than that of PBT. This result indicated that Alloy is more affected by thermal and solvent ageing. Among them, TPE2 showed the highest breakdown voltage (BDV, and it has also the highest BDV after thermal and solvent aging.

  2. Catalyst Activity Comparison of Alcohols over Zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Ramasamy, Karthikeyan K.; Wang, Yong

    2013-01-01

    Alcohol transformation to transportation fuel range hydrocarbon on HZSM-5 (SiO2 / Al2O3 = 30) catalyst was studied at 360oC and 300psig. Product distributions and catalyst life were compared using methanol, ethanol, 1-propanol or 1-butanol as a feed. The catalyst life for 1-propanol and 1-butanol was more than double compared to that for methanol and ethanol. For all the alcohols studied, the product distributions (classified to paraffin, olefin, napthene, aromatic and naphthalene compounds) varied with time on stream (TOS). At 24 hours TOS, liquid product from 1-propanol and 1-butanol transformation primarily contains higher olefin compounds. The alcohol transformation process to higher hydrocarbon involves a complex set of reaction pathways such as dehydration, oligomerization, dehydrocyclization, and hydrogenation. Compared to ethylene generated from methanol and ethanol, oligomerization of propylene and butylene has a lower activation energy and can readily take place on weaker acidic sites. On the other hand, dehydrocyclization of propylene and butylene to form the cyclic compounds requires the sits with stronger acid strength. Combination of the above mentioned reasons are the primary reasons for olefin rich product generated in the later stage of the time on stream and for the extended catalyst life time for 1 propanol and 1 butanol compared to methanol and ethanol conversion over HZSM-5.

  3. Enzymatic Hydrolysis of Polyester Thin Films: Real-Time Analysis of Film Mass Changes and Dissipation Dynamics.

    Science.gov (United States)

    Zumstein, Michael Thomas; Kohler, Hans-Peter E; McNeill, Kristopher; Sander, Michael

    2016-01-01

    Cleavage of ester bonds by extracellular microbial hydrolases is considered a key step during the breakdown of biodegradable polyester materials in natural and engineered systems. Here we present a novel analytical approach for simultaneous detection of changes in the masses and rigidities of polyester thin films during enzymatic hydrolysis using a Quartz Crystal Microbalance with Dissipation monitoring (QCM-D). In experiments with poly(butylene succinate) (PBS) and the lipase of Rhizopus oryzae (RoL), we detected complete hydrolysis of PBS thin films at pH 5 and 40 °C that proceeded through soft and water-rich film intermediates. Increasing the temperature from 20 to 40 °C resulted in a larger increase of the enzymatic hydrolysis rate of PBS than of nonpolymeric dibutyl adipate. This finding was ascribed to elevated accessibility of ester bonds to the catalytic site of RoL due to increasing polyester chain mobility. When the pH of the solution was changed from 5 to 7, initial hydrolysis rates were little affected, while a softer film intermediate that lead to incomplete film hydrolysis was formed. Hydrolysis dynamics of PBS, poly(butylene adipate), poly(lactic acid), and poly(ethylene terephthalate) in assays with RoL showed distinct differences that we attribute to differences in the polyester structure. PMID:26599203

  4. Hydrolysis of synthetic polyesters by Clostridium botulinum esterases.

    Science.gov (United States)

    Perz, Veronika; Baumschlager, Armin; Bleymaier, Klaus; Zitzenbacher, Sabine; Hromic, Altijana; Steinkellner, Georg; Pairitsch, Andris; Łyskowski, Andrzej; Gruber, Karl; Sinkel, Carsten; Küper, Ulf; Ribitsch, Doris; Guebitz, Georg M

    2016-05-01

    Two novel esterases from the anaerobe Clostridium botulinum ATCC 3502 (Cbotu_EstA and Cbotu_EstB) were expressed in Escherichia coli BL21-Gold(DE3) and were found to hydrolyze the polyester poly(butylene adipate-co-butylene terephthalate) (PBAT). The active site residues (triad Ser, Asp, His) are present in both enzymes at the same location only with some amino acid variations near the active site at the surrounding of aspartate. Yet, Cbotu_EstA showed higher kcat values on para-nitrophenyl butyrate and para-nitrophenyl acetate and was considerably more active (sixfold) on PBAT. The entrance to the active site of the modeled Cbotu_EstB appears more narrowed compared to the crystal structure of Cbotu_EstA and the N-terminus is shorter which could explain its lower activity on PBAT. The Cbotu_EstA crystal structure consists of two regions that may act as movable cap domains and a zinc metal binding site. Biotechnol. Bioeng. 2016;113: 1024-1034. © 2015 Wiley Periodicals, Inc. PMID:26524601

  5. Application of reactive siloxane prepolymers for the synthesis of thermoplastic poly(ester–siloxanes and poly(ester–ether–siloxanes

    Directory of Open Access Journals (Sweden)

    VESNA V. ANTIC

    2007-02-01

    Full Text Available Thermoplastic poly(ester–siloxanes (TPES and poly(ester–ether–siloxane s, (TPEES, based on poly(butylene terephthalate (PBT as the hard segment and different siloxane-prepolymers as the soft segments, were prepared. The TPES and TPEES were synthesized by catalyzed two-step transesterification from dimethyl terephthalate, (DMT, 1,4-butanediol, (BD and a siloxane-prepolymer. Incorporation of dicarboxypropyl- or disilanol-terminated poly(dimethylsiloxanes (PDMS into the polar poly(butylene terephthalate chains resulted in rather inhomogeneous TPES copolymers, which was a consequence of a prononuced phase separation of the polar and non-polar reactants during synthesis. Two concepts were employed to avoid or reduce phase separation: 1 the use of siloxane-containing triblock prepolymers with hydrophilic terminal blocks, such as ethylene oxide (EO, poly(propylene oxide (PPO or poly(caprolactone (PLC when the terminal blocks serve as a compatibilizer between the extremely non-polar PDMS and the polar DMT and BD, and 2 the use of a high-boiling solvent (1,2,4-trichlorobenzene during the first phase of the reaction. Homogeneity was significantly improved in the case of copolymers based on PCL–PDMS–PCL.

  6. Decay kinetics of benzophenone triplets and corresponding free radicals in soft and rigid polymers studied by laser flash photolysis.

    Science.gov (United States)

    Levin, Peter P; Efremkin, Alexei F; Sultimova, Natalie B; Kasparov, Valery V; Khudyakov, Igor V

    2014-01-01

    The kinetics of transients formed under photoexcitation of benzophenone (B) dissolved in three different polymers was studied by ns laser flash photolysis. These polymers were the soft rubbers poly (ethylene-co-butylene) (EB), polystyrene block-poly(ethylene-ran-butylene)-block-polystyrene (SEBS) and hard polystyrene (PS). We monitored the decay kinetics of triplet state (3)B(*) and of ketyl radicals BH(●). We observed exponential decay of (3)B(*) and two-stage decay kinetics of BH(●) in EB. The first stage is a fast cage recombination of a radical pair (BH(●), radical of polymer R(●)). The second slow stage of BH(●) decay follows the second-order law with a relatively high rate constant, which corresponds to recombination of BH(●) in a homogeneous liquid with a viscosity of only ~0.1 P (about five times of 2-propanol viscosity). Application of a magnetic field (MF) of 0.2 T leads to deceleration of both stages of BH(●) decay in EB by approximately 20%. Decay kinetics of both transients were observed in SEBS. There was no MF effect on BH(●) decay in SEBS. We only observed (3)B(*) in PS. Decay kinetics of (3)B(*) in this case were described as polychromatic dispersive first-order kinetics. We discuss the effects of polymer structure on transient kinetics and the MF effect.

  7. SIMULATION OF EFFECTS OF REACTIVE IMPURITIES ON PROPYLENE POLYMERIZATION IN LOOP REACTORS THROUGH GENERATION FUNCTION TECHNIQUE

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The estimation of the amount of reactive impurities in a loop reactor is of strategic importance to the propylene polymerization industry. It is essential to investigate the level of impurities in order to develop reliable monitoring and control strategies. This paper described one approach based on generation function technique with the following two steps. First, a new mechanism for propylene polymerization was proposed by considering the effects of the reactive impurities in the material on the propylene polymerization. Second, a series of equations of population balance for the propylene polymerization in loop reactors were established based on the proposed mechanism. Accordingly, the equations were transformed into the mathematic matrix through the generation function technique to investigate the effects of the reactive impurities on the propylene polymerization. Significant effects of the reactive impurities were analyzed through computational simulation. The results show that the concentration of active centre on catalysts and the polymerization conversion both decrease with the increase of the initial concentration of any reactive impurity; hydrogen concentration decreases with the increase of the initial concentration of ethylene or butylenes, whereas, it increases with the increase of the initial concentration of propadiene; the simulated weight average molecular weight and the molecular weight distribution index of polymer resins both increase with the increase of the initial concentration of ethylene or butylenes. They decrease with the increase of the initial concentration of propadiene.

  8. Isocyanate toughened pCBT: Reactive blending and tensile properties

    Directory of Open Access Journals (Sweden)

    T. Abt

    2013-02-01

    Full Text Available Cyclic butylene terephthalate oligomers (CBT were reacted in a ring-opening polymerization with three types of isocyanates: a bifunctional aromatic type, a bifunctional aliphatic type and a polymeric aromatic isocyanate. All reactions took place in a batch mixer. The use of 0.5 to 1 wt% isocyanate led to a dramatic increase in elongation at break of polymerized cyclic butylene terephthalate (pCBT, from 8 to above 100%. The stiffness and strength of the modified pCBT, however, were found to slightly decrease. Proton nuclear magnetic resonance (NMR analysis shows that the formation of thermally stable amide groups is the dominant chain extension reaction mechanism. Gel content measurements suggest a linear structure for samples containing bifunctional isocyanates while pCBT modified with polyfunctional isocyanate exhibited some gel formation at higher isocyanate content. Melting and crystallization temperatures as well as degree of crystallinity were found to decrease with increasing isocyanate content. No phase separation was detected by scanning electron microscopy (SEM analysis. Moreover, a high degree of polymerization is deduced due to the absence of CBT oligomer crystals.

  9. 催化剂对二元醇伯仲羟基氨酯化反应的影响%Effect of the Catalyst on the Urethane Reaction Selectivity of Different Hydroxyl in Diol

    Institute of Scientific and Technical Information of China (English)

    王顺平; 杨鹏飞; 赵超; 李俊英; 李天铎

    2012-01-01

    The urethane reaction of 1,2-propylene glycol or 1,3-butylene glycol with phenyl isocyanate was investigated with toluene,butyl acetate or N,N-dimethylformamide as solvents and trimethylamine(TEA) or 1,4-Diazabicyclooctane(DABCO) as catalyst,respectively.A comparative research between the primary and secondary hydroxyl groups in diol was done.It showed that the reactivity difference between the two hydroxyl groups was affected by amine catalyst.The reactivity difference of hydroxyl groups in 1,2-propylene glycol was nearly 11 when TEA was used as catalyst and toluene was used as solvent.When reacting with phenyl isocyanate at the same condition,1,3-butylene glycol showed similar rate constants compared with 1,2-propylene glycol,the reactivity difference of primary and secondary hydroxyl group in 1,3-butylene glycol was also very similar to 1,2-propylene glycol.%分别以甲苯、乙酸丁酯和N,N-二甲基甲酰胺作溶剂,以三乙胺(TEA)、1,4-二氮杂二环[2.2.2]辛烷(DABCO)作催化剂,进行1,2-丙二醇、1,3-丁二醇与苯基异氰酸酯的反应。用在线红外光谱监测反应过程,研究了二元醇中不同类型羟基的反应活性。结果表明,催化剂能够扩大伯羟基与仲羟基的反应活性差异。以甲苯作溶剂、TEA作催化剂时,1,2-丙二醇中伯羟基与仲羟基的活性差异最大,可达11倍左右。在相同条件下与苯基异氰酸酯反应时,1,2-丙二醇、1,3-丁二醇的反应速率相近,两者伯羟基与仲羟基的活性差异也相近。

  10. 高效液相色谱在葡萄糖加氢裂解中的应用%The Application of HPLC in Glucose Hydrogenation Cracking

    Institute of Scientific and Technical Information of China (English)

    罗文杰; 闫锁; 陈世鑫; 陆启明; 仵闫闫

    2012-01-01

    Taking glucose as raw material,with catalysts,the reaction liguid contained 1,2-propanediol,propylene glycol,glycols,2,3-butylene glycol,1,2-butylene glycol,1,4-butylene glycol(be called binary alcohol,sorbic alcohol,third three alcohol,formic acid for short hereinafter) stopping,(be called restructuring share for short under) acetic acid salt,lactate and others,was got through hydrogenation crauking Adopting Aminex HPX-87H Lon exclusion colour spectrum post,0.006 mol/L sulfuric acid as mobile under flow rate of 0.5 mL/min,by the differential refractive power chemistry detector checks,be able to separate binary alcohol in reaction liquid as well as restructuring share was complete,assume and a linearity without exception within certain mass thickness range.The coefficient of recovery owing method binary alcohol and restructuring share in analysing reaction liquid was 97%~103%.The method was able to determine middle binary reaction liquid alcohol and the contents re-organizing share speedy and accurately.%对于以葡萄糖为原料,在催化剂的作用下,通过加氢裂解得到含有1,2-丙二醇、乙二醇、2,3-丁二醇、1,2-丁二醇、1,4-丁二醇(以下简称二元醇)、山梨醇、丙三醇、甲酸盐、乙酸盐、乳酸盐以及其他未知物(以下简称重组份)的反应液,采用AminexHPX-87H Lon exclusion色谱柱,以0.006 mol/L的硫酸作为流动相,在流速0.5 mL/min的流量下,经示差折光化学检测器检测,能够将反应液中的二元醇以及重组份完全分离,且均在一定质量浓度范围内呈线性[1]。该方法分析反应液中的二元醇及重组份的回收率在97%~103%之间。本方法能够快速、精确测定反应液中二元醇与重组份的含量。

  11. Biodegradable polyester-based eco-composites containing hemp fibers modified with macrocyclic oligomers

    Science.gov (United States)

    Conzatti, Lucia; Utzeri, Roberto; Hodge, Philip; Stagnaro, Paola

    2016-05-01

    An original compatibilizing pathway for hemp fibers/poly(1,4-butylene adipate-co-terephtalate) (PBAT) eco-composites was explored exploiting the capability of macrocyclic oligomers (MCOs), obtained by cyclodepolymerization (CDP) of PBAT at high dilution, of being re-converted into linear chains by entropically-driven ring-opening polymerization (ED-ROP) that occurs simply heating the MCOS in the bulk. CDP reaction of PBAT was carried out varying solvent, catalyst and reaction time. Selected MCOs were used to adjust the conditions of the ED-ROP reaction. The best experimental conditions were then adopted to modify hemp fibers. Eco-composites based on PBAT and hemp fibers as obtained or modified with PBAT macrocyclics or oligomers were prepared by different process strategies. The best fiber-PBAT compatibility was observed when the fibers were modified with PBAT oligomers before incorporation in the polyester matrix.

  12. Application of radiation technology to develop green tea leaf as a natural resource for the cosmetic industry

    Science.gov (United States)

    Byun, Myung Woo; Jo, Cheorun; Lee, Ju Woon; Jo, Sung Kee; Kim, Kwan Soo

    2004-09-01

    The irradiation of natural resources such as green tea leaf, persimmon leaf, licorice root and stolon or Lonicera japonica improved the color of the extract, resulting in a higher applicability without any adverse change to the beneficial functions such as the inhibitory effects of oxidation, melanin hyperpigmentation on the skin, and others. To investigate the application of irradiated natural resources for a real cosmetic composition, the physiological activities of irradiated green tea leaf extract powder dissolved in butylene glycol and ethanol were compared to a commercial green tea extract product. Furthermore, a cream lotion was manufactured using the powder and the physiological activities were compared. Results showed that the irradiation of the green tea leaf extract and the freeze-dried powder from the extract had the same physiological activities as the commercial product in a cosmetic composition.

  13. Mechanical and Antibacterial Properties of Injection Molded Polypropylene/TiO2 Nano-Composites: Effects of Surface Modification

    Institute of Scientific and Technical Information of China (English)

    Mirigul Altan; Huseyin Yildirim

    2012-01-01

    Polypropylene (PP)/titanium dioxide (TiO2) nano-composites were prepared by melt compounding with a twin screw extruder. Nanoparticles were modified prior to melt mixing with maleic anhydride grafted styreneethylene-butylene-styrene (SEBS-g-MA) and silane. The composites were injection molded and mechanical tests were applied to obtain tensile strength, elastic modulus and impact strength. Antibacterial efficiency test was applied on the injection molded composite plaques by viable cell counting technique. The results showed that the composites including SEBS-g-MA and silane coated TiO2 gave better mechanical properties than the composites without SEBS-g-MA. Antibacterial efficiency of the composites varied according to the dispersion and the concentration of the particles and it was observed that composites at low content of TiO2 showed higher antibacterial property due to the better photocatalytic activity of the particles during UV exposure.

  14. Luminescence-Based Spectroelectrochemical Sensor for [Tc(dmpe)3]2+/+ (dmpe = 1,2-bis(dimethylphosphino)ethane) within a Charge-Selective Polymer Film

    Energy Technology Data Exchange (ETDEWEB)

    Chatterjee, Sayandev; Del Negro, Andrew S.; Edwards, Matthew K.; Bryan, Samuel A.; Kaval, Necati; Pantelic, Nebojsa; Morris, Laura K.; Heineman, W. R.; Seliskar, Carl J.

    2011-03-01

    A spectroelectrochemical sensor consisting of an indium tin oxide (ITO) optically transparent electrode (OTE) coated with a thin film of sulfonated polystyrene-blockpoly(ethylene-ran-butylene)-block-polystyrene (SSEBS) was developed for [Tc(dmpe)3]+.. [Tc(dmpe)3]+ preconcentrated by ion-exchange into the SSEBS film after 20 min exposure to aqueous [Tc(dmpe)3]+ solution, resulting in a 14-fold increase in cathodic peak current compared to a bare OTE. Colorless [Tc(dmpe)3]+ was reversibly oxidized to colored [Tc(dmpe)3]2+ by cyclic voltammetry. Detection of [Tc(dmpe)3]2+ was accomplished by electrochemically cycling the complex between non-emissive [Tc(dmpe)3]+ and emissive [Tc(dmpe)3]2+ and monitoring the modulated emission (λexc = 532 nm; λem = 660 nm). The sensor gave a linear response over the range of 0.16 to 340.0 µM.

  15. The influence of polychromic light on the surface of MDI based polyurethane elastomer

    Science.gov (United States)

    Rosu, Dan; Ciobanu, Constantin; Rosu, Liliana; Teaca, Carmen-Alice

    2009-09-01

    A polyurethane elastomer was synthesized starting from 4,4' diphenylmethane diisocyanate and poly(ethyleneadipate)diol. Butylene glycol was used as chain extender. Surface properties after photo-degradation of the elastomer under the action of the radiation with λ > 300 nm was monitored by FT-IR spectroscopy and contact angle measurements. The quality of polymer surface was observed under optical microscope. The formation of photo-Fries rearrangement and Norrish II reaction products during irradiation was associated with the gloss loss (from 100% for non-irradiated sample to 27% after 200 h irradiation time) and modification of wettability. There were also found significant modifications with irradiation time of both the glass transition temperature ( Tg decreases from 64 °C for non-irradiated sample to 53 °C after 200 h irradiation) and the swelling coefficient (an increase from 1.2% up to 2.5% is observed after 200 h irradiation).

  16. The influence of polychromic light on the surface of MDI based polyurethane elastomer

    Energy Technology Data Exchange (ETDEWEB)

    Rosu, Dan, E-mail: drosu@icmpp.ro [' Petru Poni' Institute of Macromolecular Chemistry, 41A Gr. Ghica-Voda Alley, Iasi, 700487 Romania (Romania); Ciobanu, Constantin; Rosu, Liliana; Teaca, Carmen-Alice [' Petru Poni' Institute of Macromolecular Chemistry, 41A Gr. Ghica-Voda Alley, Iasi, 700487 Romania (Romania)

    2009-09-15

    A polyurethane elastomer was synthesized starting from 4,4' diphenylmethane diisocyanate and poly(ethyleneadipate)diol. Butylene glycol was used as chain extender. Surface properties after photo-degradation of the elastomer under the action of the radiation with {lambda} > 300 nm was monitored by FT-IR spectroscopy and contact angle measurements. The quality of polymer surface was observed under optical microscope. The formation of photo-Fries rearrangement and Norrish II reaction products during irradiation was associated with the gloss loss (from 100% for non-irradiated sample to 27% after 200 h irradiation time) and modification of wettability. There were also found significant modifications with irradiation time of both the glass transition temperature (T{sub g} decreases from 64 deg. C for non-irradiated sample to 53 deg. C after 200 h irradiation) and the swelling coefficient (an increase from 1.2% up to 2.5% is observed after 200 h irradiation).

  17. Lignin-based cement fluid loss control additive

    Energy Technology Data Exchange (ETDEWEB)

    Schilling, P.

    1990-05-22

    This patent describes a hydraulic cement slurry composition. It comprises: a hydraulic cement, and the following expressed as parts by weight per 100 parts of the hydraulic cement, water from about 25 to 105 parts, and from abut 0.5 to 2.5 parts of a compound selected from the group consisting of a sulfonated lignin and a sulfomethylated lignin, wherein the lignin has been sequentially crosslinked by reacting the lignin with a member of the group consisting of formaldehyde and epichlorohydrin and alkoxylated with between about 2 to about 6 moles of a compound selected from the group consisting of ethylene oxide, propylene oxide, butylene oxide and a combination thereof per 1000 g of the lignin.

  18. Effects of P content in a P/HZSM-5 catalyst on the conversion of ethanol to hydrocarbons

    Institute of Scientific and Technical Information of China (English)

    Jiangyin Lu; Yancong Liu

    2011-01-01

    A series of P/HZSM-5 catalysts prepared by impregnation method were used for ethanol conversion to lower olefins.The catalysts were characterized by X-ray diffraction(XRD),NH3-temperature-programmed desorption(NH3-TPD)and N2 adsorption-desorption measurements.It was found that the P/HZSM-5 catalysts showed high activity and selectivity toward light olefins.The selectivities of propylene and butylene can be improved with the introduction of phosphorus(P).When the content of P reached 3.0 wt%,more than 18.9% propylene in the gaseous products was obtained over the P/HZSM-5 catalyst at 450 ℃.The introduction of P modified the strong Br()nsted acid sites of the original HZSM-5 catalysts and P/HZSM-5 catalysts could resist coke formation and showed good stability.

  19. Mechanism of nanocapsules of Matricaria recutita L. extract formation by the emulsion-diffusion process

    Science.gov (United States)

    Esmaeili, Akbar; Saremnia, Betsabe; Koohian, Ata; Rezazadeh, Shamsali

    2011-10-01

    Nanocapsules coated by medicinal plants have many applications in drug manufacturing. Medicinal plants can be loaded on nanocapsules with polyesteric triblock copolymer poly ethylene glycol-poly butylene adipate-poly ethylene glycol (PEG-PBA-PEG) as shell and olive oil can be introduced as a core of nanocapsules by a method known as polymer deposition solvent evaporation method. In this research, first, certain amount of polymer, Matricaria recutita extract and olive oil were mixed with acetone and then, water was added to the solution using magnetic stirrer. After which the acetone was removed by vacuuming and finally nanocapsules were found by freezing-drier. The study showed the size of nanocapsules depends on variety of factors such as the ratio of polymer to oil and concentration of polymers and plant extract. The nanocapsules were identified by scanning electron microscopy (SEM) and zeta potential sizer (ZPS), Fourier-transform infrared spectroscopy (FT-IR), and nuclear magnetic resonance (NMR).

  20. A "catalyst switch" Strategy for the sequential metal-free polymerization of epoxides and cyclic Esters/Carbonate

    KAUST Repository

    Zhao, Junpeng

    2014-06-24

    A "catalyst switch" strategy was used to synthesize well-defined polyether-polyester/polycarbonate block copolymers. Epoxides (ethylene oxide and/or 1,2-butylene oxide) were first polymerized from a monoalcohol in the presence of a strong phosphazene base promoter (t-BuP4). Then an excess of diphenyl phosphate (DPP) was introduced, followed by the addition and polymerization of a cyclic ester (ε-caprolactone or δ-valerolactone) or a cyclic carbonate (trimethylene carbonate), where DPP acted as both the neutralizer of phosphazenium alkoxide (polyether chain end) and the activator of cyclic ester/carbonate. This work has provided a one-pot sequential polymerization method for the metal-free synthesis of block copolymers from monomers which are suited for different types of organic catalysts. © 2014 American Chemical Society.

  1. Using glycerol produced from biodiesel as a plasticiser in extruded biodegradable films

    Directory of Open Access Journals (Sweden)

    Ana Paula Bilck

    2015-08-01

    Full Text Available AbstractThe demand for renewably sourced biodegradable materials has increased the need to produce materials that combine appropriate functional properties at competitive costs. Thermoplastic starch and polyester blends are an interesting alternative to current materials due to the low cost of starch and the functional properties and processability of the resulting blends. Producing thermoplastic starch (TPS requires using a plasticiser at concentrations between 20 and 30%wt (in relation to starch. Glycerol is the most common plasticiser due to its high plasticising capacity and thermal stability at processing temperatures. The objective of this study was to evaluate glycerol waste from the biodiesel industry, with different degrees of purification, as plasticisers for TPS / poly (butylene adipate-co-terephthalate (PBAT blends. Different purities of glycerol produced films with similar mechanical, optical and barrier properties to those made with purified glycerol (99.7%. Therefore, crude glycerol is a renewable alternative plasticiser that reduces the cost of plasticisation by 6-fold.

  2. Effects of SEBS-g-MAH on the properties of injection moulded poly(lactic acid/nano-calcium carbonate composites

    Directory of Open Access Journals (Sweden)

    W. S. Chow

    2012-06-01

    Full Text Available Poly(lactic acid/nano-precipitated calcium carbonate (PLA/NPCC composites toughened with maleated styrene-ethylene/butylene-styrene (SEBS-g-MAH were prepared by melt-compounding on a co-rotating twin-screw extruder followed by injection moulding. The mechanical properties of the PLA nanocomposites were characterized by tensile, flexural and impact tests, while their morphology were investigated using transmission electron microscopy (TEM. The thermal properties of the composites were examined with differential scanning calorimeter (DSC and thermogravimetric analyzer (TGA. The elongation at break and impact strength of the PLA/NPCC nanocomposites increased significantly after addition of SEBS-g-MAH. Both nano-dispersed NPCC and small NPCC clusters were found in PLA matrix. Also, some SEBS-g-MAH encapsulated NPCC can be observed. Thermal stability of PLA/NPCC was enhanced prominently by the addition of SEBS-g-MAH.

  3. Determination of constituents of essential oil from Angelica sinensis by gas chromatography-mass spectrometry

    Institute of Scientific and Technical Information of China (English)

    WU Ming-jian; SUN Xian-jun; DAI Yuan-hui; GUO Fang-qiu; HUANG Lan-fang; LIANG Yi-zeng

    2005-01-01

    Gas chromatography-mass spectrometry (GC-MS) coupled with chemometric resolution upon two-dimensional data was employed to analyze the constituents of essential oils of Angelica sinensis. Constituents in essential oils of Angelica sinensis root were identified by GC-MS with the help of subwindow factor analysis (SFA) method resolving two-dimensional original data into mass spectra and chromatograms. 76 of 97 separated constituents in essential oil of Angelica sinensis root were identified and quantified, and they account for about 91.36% of the total content. The results show that ligustilide, butylene phthalide, 2-methoxy-4-vinylphenol, carvacrol, allo-ocimene,2,6,6-trimethylbicyclo-[3,1,1]hept-2-ene are the main constituents in essential oil of Angelica sinensis root.

  4. 重油催化裂解汽柴油二次裂解性能研究%Secondary Cracking of Gasoline and Diesel from Heavy Oil Catalytic Pyrolysis

    Institute of Scientific and Technical Information of China (English)

    刘植昌; 孟祥海; 徐春明; 高金森

    2007-01-01

    This paper investigated the secondary cracking of gasoline and diesel from the catalytic pyrolysis of Daqing atmospheric residue on catalyst CEP-1 in a fluidized bed reactor.The results show that the secondary cracking reactivity of gasoline and diesel is poor, and the yield of total light olefins is only about 10% (by mass).As reaction temperature increases, ethylene yield increases, butylene yield decreases, and propylene yield shows a maximum.The optimal reaction temperature is about 670 ℃ for the production of light olefins.With the enhancement of catalyst-to-oil mass ratio and steam-to-oil mass ratio, the yields of light olefins increase to some extent.About 6.30% of the mass of total aromatic rings is converted by secondary cracking, indicating that aromatic hydrocarbons are not easy to undergo ring-opening reactions under the present experimental conditions.

  5. Significant Breakthrough in Industrial Test of the "Methanol to Olefins" Process Developed by Dalian Institute of Chemical Physics, Chinese Academy of Sciences

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    @@ A process of "Methanol or Dimethylether to Olefins" developed by Dalian Institute of Chemical Physics (DICP), designated as the DMTO process, has attained great success in industrial scaling up testing. DICP, by collaborating with the Xinxing Coal Chemical Co., Ltd. of Shaanxi Province and the Luoyang Petrochemical Engineering Co. of the SINOPEC Group, operated successfully a 50t(methanol)/d unit for the conversion of methanol to lower olefins, with a methanol conversion of close to 100%, and a selectivity to lower olefins(ethylene, propylene and butylenes) of higher than 90%. On 23rd August, the industrial test project has passed a state appraisal. The experts of the Appraisal Group, headed by Prof.

  6. Study on reformulation of fluid catalytic cracking gasoline and increasing production of light olefins

    Institute of Scientific and Technical Information of China (English)

    Pingxiang YAN; Xianghai MENG; Jinsen GAO; Chunmin XU; Zhiyu SUI

    2008-01-01

    The effects of reaction temperature, mass ratio of catalyst to oil, space velocity, and mass ratio of water to oil on the product distribution, the yields of light olefins (light olefins including ethylene, propylene and butylene) and the composition of the fluid catalytic cracking (FCC) gasoline upgraded over the self-made catalyst GL in a confined fluidized bed reactor were investigated. The experimental results showed that FCC gasoline was obviously reformulated under appropriate reaction con-ditions. The olefins (olefins with C atom number above 4) content of FCC gasoline was markedly reduced, and the aromatics content and octane number were increased. The upgraded gasoline met the new standard of gasoline, and meanwhile, higher yields of light olefins were obtained. Furthermore, higher reaction temperature, higher mass ratio of catalyst to oil, higher mass ratio of water to oil, and lower space velocity were found to be beneficial to FCC gasoline reformulation and light olefins production.

  7. Mechanical Properties and Morphology of the Clay/Waterborne Polyurethane Nanocomposite

    Institute of Scientific and Technical Information of China (English)

    ZHANG Yongcheng; WANG Junwei; ZHAO Yuhua; KANG maoqing; WANG Xinkui

    2006-01-01

    Stable clay/waterborne polyurethane nanocompostie dispersions were synthesized by sulfonated poly ( butylene adipate ) diol , 4,4-diphenylmethane diisocyanate , dimethyl propionic acid, 1,4-butanediol, triethyl anine and clay-water dispersion through a route named prepolymer acetone mixing progress. The reinforced mechanical properties and thermal resistance of films casting from it were examined by dynamic mechanical analyses (DMA), thermogravimetric analyses (TGA) and tensile tests. Furthermore, the morphology of these nanocompostie films and dispersions were observed by transmission electron microscopy (TEM), scanning electron microscopy( SEM), wide-angle X-ray diffraction analyses( WXRD ). The experimental results reveal that the clay could be predominantly dispersed in the pristine polymer forming nanocomposties, and evidendy enhanced the tensile properties and modulus of it. Additionally, the best-reinforced effect could occur when the clay content was near 1 wt% .

  8. Networks of gel-forming triblock copolymer solutions: In situ SANS and rheological measurements

    DEFF Research Database (Denmark)

    Mortensen, K.; Almdal, K.; Kleppinger, R.;

    1998-01-01

    Triblock copolymers in a solvent, selective for their middle blocks provide the basis for the formation of novel physical networks where cross-links are formed by self-assembled domains of the end-blocks. Triblock copolymers of poly(styrene)-poly(ethylene,butylene)-poly(styrene) (SEBS) dissolved...... in a mixture of aliphatic and alicyclic compounds constitute such a network system. Using a Rheometrics RSA-2 instrument modified for in situ measurements of small-angle neutron scattering and rheology provides a unique possibility far detailed understanding thermodynamics of such a gel. The self......-association of the PS-blocks do not only promote formation of highly inter-connected end-block domains, but within a narrow temperature range these domains furthermore constitute a network with body-centered cubic (BCC) microstructure. Upon large amplitude oscillating shear the polycrystalline soft gel can be aligned...

  9. Morphology and Dynamic Mechanical Properties of Styrene Containing Tri-Block Copolymers for Electromagnetic Wave Interaction Applications

    Science.gov (United States)

    Peddini, S.; Mauritz, K.; Nikles, D.; Weston, J.

    2008-03-01

    Styrene containing triblock copolymers, namely poly(styrene-ethylene/butylene-styrene) (SEBS) and poly(styrene-butadiene-styrene)] (SBS), were selectively modified by attaching polar groups to facilitate the in-growth of an inorganic component. In case of SEBS, the styrene block was sulfonated, and in SBS, the butadiene block was hydroxylated. The extent of modification was determined by analytical and spectroscopic methods. This presentation shows the morphology and dynamical mechanical properties of both block copolymers before and after modification. Nanocomposites of these block copolymers were prepared by inclusion of magnetic metal oxides via an in-situ precipitation and self assembly processes and their morphology and dynamical mechanical properties were studied. Magnetic properties of these polymers filled with iron oxide nanoparticles were measured using an alternating gradient magnetometer (AGM) at room temperature to observe the magnetic hysteresis.

  10. Silica reinforced triblock copolymer gels

    DEFF Research Database (Denmark)

    Theunissen, E.; Overbergh, N.; Reynaers, H.;

    2004-01-01

    The effect of silica and polymer coated silica particles as reinforcing agents on the structural and mechanical properties of polystyrene-poly(ethylene/butylene)-polystyrene (PS-PEB-PS) triblock gel has been investigated. Different types of chemically modified silica have been compared in order...... to evaluate the influence of the compatibility between gel and filler. Time-resolved SANS and small-angle X-ray scattering (SAXS) shows that the presence of silica particles affects the ordering of the polystyrene domains during gelsetting. The scattering pattern of silica-reinforced gels reveals strong...... scattering at very low q, but no structure and formfactor information. However, on heating above the viscoelastic to plastic transition, the 'typical' scattering pattern of the copolymer gel builds-up. All reinforced gels are strengthened by the addition of the reinforcing agent. The transitions from...

  11. Application of radiation technology to develop green tea leaf as a natural resource for the cosmetic industry

    International Nuclear Information System (INIS)

    The irradiation of natural resources such as green tea leaf, persimmon leaf, licorice root and stolon or Lonicera japonica improved the color of the extract, resulting in a higher applicability without any adverse change to the beneficial functions such as the inhibitory effects of oxidation, melanin hyperpigmentation on the skin, and others. To investigate the application of irradiated natural resources for a real cosmetic composition, the physiological activities of irradiated green tea leaf extract powder dissolved in butylene glycol and ethanol were compared to a commercial green tea extract product. Furthermore, a cream lotion was manufactured using the powder and the physiological activities were compared. Results showed that the irradiation of the green tea leaf extract and the freeze-dried powder from the extract had the same physiological activities as the commercial product in a cosmetic composition

  12. Application of electron accelerator for thin film in Indonesia

    International Nuclear Information System (INIS)

    Electron accelerator is widely used for the crosslinking of wire and cable insulation, the treatment of heat shrinkable products, precuring of tire components, and the sterilization of medical products. Research and development the use of electron accelerator for thin film in Indonesia covered radiation curing of surface coating, crosslinking of poly (butylenes succinate), crosslinking of wire, cable and heat shrinkable, sterilization of wound dressing, and prevulcanization of tire. In general, comparing with conventional method, electron beam processing have some advantages, such as, less energy consumption, much higher production rate, processing ability at ambient temperature and environmental friendly. Indonesia has a great potential to develop the application of electron accelerator, due to the remarkable growth industrial sector, the abundant of natural resources and the increasing demand of the high quality products. This paper describes the activities concerning with R and D, and application of electron accelerator for processing of thin film. (author)

  13. Absorbance-based spectroelectrochemical sensor for [Re(dmpe)3]+ (dmpe = dimethylphosphinoethane)

    Energy Technology Data Exchange (ETDEWEB)

    Morris, Laura K; Seliskar, Carl J; Heineman, William R; Del Negro, Andrew S; Bryan, Samuel A

    2009-10-01

    A spectroelectrochemical sensor was developed for [Re(dmpe)3]+ as a non radioactive analog for [Tc(dmpe)3]+. The sensor consists of an optically transparent electrode (OTE) coated with a thin film of sulfonated polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SSEBS). Colorless [Re(dmpe)3]+ was reversibly oxidized to [Re(dmpe)3]2+ (λmax = 530 nm). [Re(dmpe)3]+ preconcentrated by ion-exchange into the SSEBS film, resulting in a 20-fold increase in peak current compared to a bare OTE after 1 h of exposure to aqueous [Re(dmpe)3]+ solution. Detection of [Re(dmpe)3]+ at concentrations down to 2 x 10 6 M was accomplished by electrochemical modulation of the complex and monitoring absorbance by attenuated total reflectance (ATR).

  14. Biodegradable starch-based films containing saturated fatty acids: thermal, infrared and raman spectroscopic characterization

    Directory of Open Access Journals (Sweden)

    Marcelo M. Nobrega

    2012-01-01

    Full Text Available Biodegradable films of thermoplastic starch and poly (butylene adipate co-terephthalate (PBAT containing fatty acids were characterized thermally and with infrared and Raman spectroscopies. The symmetrical character of the benzene ring in PBAT provided a means to illustrate the difference between these spectroscopic techniques, because a band appeared in the Raman spectrum but not in the infrared. The thermal analysis showed three degradation stages related to fatty acids, starch and PBAT. The incorporation of saturated fatty acids with different molecular mass (caproic, lauric and stearic did not change the nature of the chemical bonds among the components in the blends of starch, PBAT and glycerol, according to the thermal analysis, infrared and Raman spectroscopies.

  15. Evaluation of biodegradable plastics for rubber seedling applications

    Science.gov (United States)

    Mansor, Mohd Khairulniza; Dayang Habibah A. I., H.; Kamal, Mazlina Mustafa

    2015-08-01

    The main negative consequence of conventional plastics in agriculture is related to handling the wastes plasticand the associated environmental impact. Hence, a study of different types of potentially biodegradable plastics used for nursery applications have been evaluated on its mechanical,water absorption propertiesand Fourier transform infra-red (FTIR) spectroscopy. Supplied samples from different companies were designated as SF, CF and CO. Most of the polybags exhibited mechanical properties quite similar to the conventional plastics (polybag LDPE). CO polybag which is based on PVA however had extensively higher tensile strength and water absorption properties. FTIR study revealed a characteristics absorbance of conventional plastic, SF, CF and CO biodegradable polybag are associated with polyethylene, poly(butylene adipate-co-terephthalate) (PBAT), polyethylene and polyvinyl alcohol (PVA) structures respectively.

  16. One-pot synthesis of linear- and three-arm star-tetrablock quarterpolymers via sequential metal-free ring-opening polymerization using a "catalyst switch" strategy

    KAUST Repository

    Zhao, Junpeng

    2014-08-06

    A "catalyst switch" strategy has been used to sequentially polymerize four different heterocyclic monomers. In the first step, epoxides (1,2-butylene oxide and ethylene oxide) were successively polymerized from a monohydroxy or trihydroxy initiator in the presence of a strong phosphazene base promoter (t-BuP4). Then, an excess of diphenyl phosphate (DPP) was introduced, followed by addition and polymerization of a cyclic carbonate (trimethylene carbonate) and a cyclic ester (δ-valerolactone or ε-caprolactone). DPP acted as both neutralizer of the phosphazenium alkoxide (polyether chain end) and activator of the cyclic carbonate/ester. Using this method, linear- and star-tetrablock quarterpolymers were prepared in one pot. This work is emphasizing the strength of the previously developed catalyst switch strategy for the facile metal-free synthesis of complex macromolecular architectures. © 2014 Wiley Periodicals, Inc.

  17. Advances in catalytic production of bio-based polyester monomer 2,5-furandicarboxylic acid derived from lignocellulosic biomass.

    Science.gov (United States)

    Zhang, Junhua; Li, Junke; Tang, Yanjun; Lin, Lu; Long, Minnan

    2015-10-01

    Recently, the production and utilization of 2,5-furandicarboxylic acid (FDCA) have become a hot research topic in catalyst field and polyester industry for its special chemical structure and a wide range of raw material source. FDCA is a potential replacement for the terephthalic acid monomer used in the production of poly(ethylene terephthalate) (PET) and poly(butylene terephthalate) (PBT), which opens up a new pathway for obtaining biomass-based polyester to replace or partially replace petroleum based polyester. Here, we mainly reviewed the catalytic pathway for the synthesis of FDCA derived from lignocellulosic biomass or from the related downstream products, such as glucose, 5-hydroxymethylfurfural (HMF). Moreover, the utilization of oxidation catalysts, the reaction mechanism, the existing limitations and unsolved challenges were also elaborated in detail. Therefore, we hope this mini review provides a helpful overview and insight to readers in this exciting research area. PMID:26076643

  18. Synthesis and Drug Release Properties of Thermosensitive Poly(N-vinylacetamide-co-vinylacctate) Hydrogels

    Institute of Scientific and Technical Information of China (English)

    YANG Li-he; CHU Hong; CHEN Ming-qing; HU Na; ZHAO Yi-fan

    2011-01-01

    Thermosensitive poly[N-vinylacetamide-co-vinylacetate][P(NVA-co-VAc)] hydrogels were prepared via free radical copolymerization from hydrophilic NVA and hydrophobic VAc in the presence of butylenes-bis (N-vinylacetamide)(Bis-NVA) as crosslinker. Scanning electron microscopy(SEM) images reveal that the as-prepared hydrogels were of three-dimensional network with irregular cave structure. The prepared hydrogels with more NVA in the feed swelled faster and the swelling ratio of the hydrogels gradually decreased with temperature increasing from 10 ℃ to 60 ℃. The dynamic swelling studies indicate that the swelling process of the hydrogels was controlled by diffusion of water molecules considered as Fickian-controlled case. The adsorption amount of model drug, sodium salicylate(SS) was higher in the hydrogels containing more NVA units, whose corresponding release could reach equilibrium in about 6 h.

  19. Complementary study of molecular dynamics and domain sizes in heterogenous nanocomposites PBT/DA-C60 and PBT/TCNEO-C60

    International Nuclear Information System (INIS)

    A comprehensive study of molecular dynamics and structure in new heterogenous nanocomposites based on poly(butylene terephthalate) and nanoparticles C60 modified by n-decylamine or tetracyanoethylene oxide has been performed. The domain structure of new nanocomposites has been investigated by Fourier transform infrared spectroscopy, wide-angle X-ray scattering, and differential scanning calorimetry techniques. Solid-state 1H NMR techniques were used to study molecular dynamics and domain sizes in new nanocomposites. Information about the electronic properties of these nanocomposites was obtained by means of electron paramagnetic resonance method. It was shown that the structure and molecular dynamics of new nanocomposites were strongly dependent on the properties and concentration of fullerene derivates.

  20. Hybrid ion-exchange membranes for fuel cells and separation processes

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez-Carretero, F.J.; Compan, V. [Departamento de Termodinamica Aplicada, ETSII, Universidad Politecnica de Valencia, 46020 Valencia (Spain); Riande, E. [Instituto de Ciencia y Tecnologia de Polimeros (CSIC), 28006 Madrid (Spain)

    2007-11-08

    This work reports the preparation and characterization of hybrid membranes cast from dispersions of inorganic fillers in sulfonated polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene solutions. Silica gel, SBA-15 and sepiolite, all of them functionalized with phenylsulfonic acid groups, were used as fillers. For comparative purposes, the performance of composite membranes cast from dispersions of functionalized inorganic fillers in Nafion {sup registered} solutions was investigated. Inspection of the texture of the membranes by using SEM techniques shows that the fillers are better dispersed in sulfonated polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene than in Nafion {sup registered}. The value of the water uptake for the membranes prepared from the former polyelectrolyte is in most cases at least three times that measured for hybrid Nafion {sup registered} membranes. The conductivity of the membranes was measured at 80 C by impedance spectroscopy obtaining values of 3.44, 6.90 and 3.54 S m{sup -1} for the hybrid membranes based on the triblock copolymer containing functionalized silica gel, SBA-15 and sepiolite fillers, respectively. These results compare very favourably with those obtained at 80 C for Nafion {sup registered} hybrid membranes containing silica gel, SBA-15 and sepiolite, all of them fuctionalized with phenylsulfonic acid groups, whose conductivities are, 2.84, 6.75 and 3.31 S m{sup -1}, respectively. Resistance measurements carried out under controlled humidity conditions show that the conductivity of sulfonated triblock copolymer membranes containing functionalized SBA-15 filler undergoes a rather sharp increase when they are conditioned under an atmosphere of 75%, or larger, relative humidity. (author)

  1. Enhancing the Mechanical Properties of Biodegradable Polymer Blends Using Tubular Nanoparticle Stitching of the Interfaces.

    Science.gov (United States)

    Guo, Yichen; He, Shan; Yang, Kai; Xue, Yuan; Zuo, Xianghao; Yu, Yingjie; Liu, Ying; Chang, Chung-Chueh; Rafailovich, Miriam H

    2016-07-13

    "Green" polymer nanocomposites were made by melt blending biodegradable poly(lactic acid) (PLA) and poly(butylene adipate-co-butylene terephthalate) (PBAT) with either montmorillonite clays (Cloisite Na(+)), halloysite nanotubes (HNTs), the resorcinol diphenyl phosphate (RDP)-coated Cloisite Na(+), and coated HNTs. A technique for measuring the work of adhesion (Wa) between nanoparticles and their matrixes was used to determine the dispersion preference of the nanoparticles in the PLA/PBAT blend system. Transmission electron microscopy (TEM) images of thin sections indicated that even though both RDP-coated nanotubes and clay platelets segregated to the interfacial regions between the two immiscible polymers, only the platelets, having the larger specific surface area, were able to reduce the PBAT domain sizes. The ability of clay platelets to partially compatibilize the blend was further confirmed by the dynamic mechanical analysis (DMA) which showed that the glass transition temperatures of two polymers tended to shift closer. No shift was observed with either coated or uncoated HNTs samples. Izod impact testing demonstrated that the rubbery PBAT phase greatly increased the impact strength of the unfilled blend, but addition of only 5% of treated clay decreased the impact strength by nearly 50%. On the other hand, an increase of 9% relative to the unfilled blend sample was observed with the addition of 5% treated nanotubes. TEM cross-section analysis confirmed that the RDP-coated clay platelets covered most of the interfacial area. On one hand, this enabled them to reduce the interfacial tension effectively; on the other hand, it prevented chain entanglements across the phase boundary and increased the overall brittleness, which was confirmed by rheology measurements. In contrast, the RDP-coated HNTs were observed to lie perpendicular to the interface, which made them less effective in reducing interfacial tension but encouraged interfacial entanglements across

  2. Blends of polyester ionomers with polar polymers: Interactions, reactions, and compatibilization

    Science.gov (United States)

    Boykin, Timothy Lamar

    The compatibility of amorphous and semicrystalline polyester ionomers with various polar polymers (i.e., polyesters and polyamides) has been investigated for their potential use as minor component compatibilizers. The degree of compatibility (i.e., ranging from incompatible to miscible) between the polyester ionomers and the polar polymers was determined by evaluating the effect of blend composition on the melting behavior and phase behavior of binary blends. In addition, the origin of compatibility and/or incompatibility for each of the binary blends (i.e., polyamide/ionomer and polyester/ionomer) was determined by evaluating blends prepared by both solution and melt mixed methods. Subsequent to investigation of the binary blends, the effect of polyester ionomer addition on the compatibility of polyamide/polyester blends was investigated by evaluating the mechanical properties and phase morphology of ionomer compatibilized polyamide/polyester blends. Polyester ionomers (amorphous and semicrystalline) were shown to exhibit a high degree of compatibility (even miscibility) with polyamides, such as nylon 6,6 (N66). Compatibility was attributed to specific interactions between the metal counterion of the polyester ionomer and the amide groups of N66. The degree of compatibility (or miscibility) was shown to be dependent on the counterion type of the ionomer, with the highest degree exhibited by blends containing the divalent form of the polyester ionomers. Although polyester ionomers were shown to exhibit incompatibility with both poly(ethylene terephthalate) (PET) and poly(butylene terephthalate) (PBT), increasing the time of melt processing significantly enhanced the compatibility of the polyester ionomers with both PET and PBT. The observed enhancement in compatibility was attributed to ester-ester interchange between the polyester blend components, which was confirmed by NMR spectroscopy. The addition of polyester ionomers as a minor component compatibilizer (i

  3. Morphological Structure and Properties of PLA/PBAT/PLA-g-MAH Biodegradable Composites%PLA/PBAT/PLA-g-MAH可生物降解复合材料的形态结构与性能分析

    Institute of Scientific and Technical Information of China (English)

    周志斌; 刘跃军; 谭海英

    2016-01-01

    Poly(lactic acid)-graft-maleic anhydride (PLA-g-MAH) prepared by melt blending was used to compatiblize poly(lactic acid)/poly(butylene adipate-co-butylene terephthalate) (PLA/PBAT) blends. The structure and properties of PLA/PBAT/PLA-g-MAH composites were investigated by fourier transform infrared spectroscopy (FTIR), scanning elec-tron microscope (SEM), universal testing machine, pendulum impact tester, differential scanning calorimeter (DSC) and the hydrolysis of alkaline solution. SEM results showed that the phase interface became blurry between PLA and PBAT in PLA/PBAT blends with compatibilizer PLA-g-MAH, indicated that the PLA-g-MAH had certain compatibilized effect on PLA/PBAT blends. The incorporation of PLA-g-MAH resulted in a slight decrease of tensile strength and flexural strength compared with pure PLA, but improved impact strength and elongation at break about 17 times compared with pure PLA with added PLA-g-MAH. Moreover, the adding of PLA-g-MAH improved the biodegradability of PLA/PBAT blend.%通过熔融共混法制备马来酸酐接枝聚乳酸(PLA-g-MAH)用于改善聚乳酸/聚己二酸-对苯二甲酸丁二酯共混物(PLA/PBAT)的相容性,并对复合材料的形态结构、力学性能和生物降解性能进行研究。SEM结果显示,添加增容剂PLA-g-MAH后,PLA/PBAT共混物两相间的界面明显变得模糊,说明PLA-g-MAH对共混物有一定的增容作用;增容剂PLA-g-MAH的加入,使复合材料的拉伸强度和弯曲强度相比于纯PLA略有下降,但其冲击强度有一定程度的提高,断裂伸长率有显著提高,比纯PLA 的断裂伸长率提高了约17倍,表现出良好的力学性能;另外,PLA-g-MAH的加入提高了共混物的生物降解性能。

  4. Estudio del comportamiento mecánico de gelés físicos termorreversibles obtenidos a partir de copolímeros tribloques de PS-b-poli(etileno/butileno-PS en un disolvente selectivo del bloque central

    Directory of Open Access Journals (Sweden)

    Hernáez, E.

    2001-04-01

    Full Text Available The thermoreversible gelation of three triblock copolymers polystyrene-bpoly( ethylene/butylene-b-polystyrene, with different molar mass and a similar chemical composition, in n-octane was studied. The solvent is selective for the middle poly(ethylene/butylene block of the copolymers. The influence of the molar mass of the three copolymers on the gelation and on the mechanical properties of the gels was analysed. The sol-gel transition temperatures, Tgel, have been determined and they increase with the copolymer concentration and the copolymer molar mass. On the other hand, the mechanical properties of the different gels were examined through oscillatory shear and compressive stress relaxation measurements. The concentration dependence of the elastic storage modulus, G’, for the three copolymer studied fit a sole straight line in a doublelogarithmic scale and its slope (2.22 is close to that expected for systems in good solvents (2.25. As the temperature is near to the sol-gel transition temperature, the elastic modulus are smaller and the relaxation rates are higher.

    Se ha estudiado la influencia del peso molecular del copolímero en la formación de geles físicos termoreversibles de copolímeros tribloque de la forma poliestireno-b-poli(etileno/butileno-b-poliestireno (SEBS en n-octano y en sus propiedades mecánicas. Se ha determinado la temperatura de formación de los geles, Tgel, concluyendo que éstas aumentan con la concentración y el peso molecular del copolímero. Por otra parte, se han medido las propiedades mecánicas de los geles empleando ensayos de torsión y relajación de tensión, en función de la concentración de copolímero. La dependencia doble logarítmica del módulo G' con la concentración de copolímero para los tres SEBS se ajusta a una línea recta de pendiente 2,22, próxima a la predicha para geles preparados químicamente (2,25. Cuanto más próxima está la temperatura de medida

  5. Isolation and screening of biopolymer-degrading microorganisms from northern Thailand.

    Science.gov (United States)

    Penkhrue, Watsana; Khanongnuch, Chartchai; Masaki, Kazuo; Pathom-Aree, Wasu; Punyodom, Winita; Lumyong, Saisamorn

    2015-09-01

    Forty agricultural soils were collected from Chiang Mai and Lampang provinces in northern Thailand. Bacteria, actinomycetes and fungi were isolated and screened for their ability to degrade polylactic acid (PLA), polycaprolactone (PCL) and poly(butylene succinate) (PBS) by the agar diffusion method. Sixty-seven actinomycetes, seven bacteria and five fungal isolates were obtained. The majority of actinomycetes were Streptomyces based on morphological characteristic, chemotaxonomy and 16S rRNA gene data. Seventy-nine microorganisms were isolated from 40 soil samples. Twenty-six isolates showed PLA-degradation (32.9 %), 44 isolates showed PBS-degradation (55.7 %) and 58 isolates showed PCL-degradation (73.4 %). Interestingly, 16 isolates (20.2 %) could degrade all three types of bioplastics used in this study. The Amycolatopsis sp. strain SCM_MK2-4 showed the highest enzyme activity for both PLA and PCL, 0.046 and 0.023 U/mL, respectively. Moreover, this strain produced protease, esterase and lipase on agar plates. Approximately, 36.7 % of the PLA film was degraded by Amycolatopsis sp. SCM_MK2-4 after 7 days of cultivation at 30 °C in culture broth. PMID:26135516

  6. RADIOPHARMACEUTICALS FOR IMAGING OF HYPOXIC TUMORS: A REVIEW

    Directory of Open Access Journals (Sweden)

    Chaitanya Prasad Meher

    2012-11-01

    Full Text Available Radiopharmaceuticals are drugs containing a radionuclide and are used routinely in nuclear medicine for the diagnosis and therapy of various diseases. The mechanism of localization of the radiopharmaceutical in different organs provides the clue for designing of the agent meant for a specific organ or pathway. Various agent like F-18, Cu-64/67, I-123, and Tc-99m are used as imaging of hypoxic tumors. Of these, F-18-fluoromisonidazole and I-123-iodoazomycin arabinoside (IAZA have been most widely studied clinically. Non-nitro-containing bioreductive complexes, such as the Cu-60/62/64 thiosemicarbazone ATSM and Tc-99m butylene amineoxime (BnAO or HL91, have also been evaluated. In particular, I-123-IAZA and Cu-60-ATSM have shown correlation with response to radiotherapy in preliminary clinical studies. However, more preclinical studies comparing imaging with validated invasive methods and clinical studies with outcome measures are required. Nuclear medicine is poised to play an important role in optimizing the therapy of patients with hypoxic tumors. The present review is concern with the various radiopharmaceuticals used for imaging of hypoxia.

  7. Synthesis and Characterizations of Poly(trimethylene terephthalate-b-poly(tetramethylene glycol Copolymers

    Directory of Open Access Journals (Sweden)

    Feng Liu

    2013-01-01

    Full Text Available A series of poly(trimethylene terephthalate-b-poly(tetramethylene glycol (PTT-PTMEG copolymers were synthesized by two-step melt-polycondensation. The copolymers were characterized by using Fourier transform infrared spectroscopy (FTIR, 1H NMR spectroscopy, rheometer, differential scanning calorimetry (DSC, polarized optical microscopy (POM, thermal gravimetric analysis (TGA, and mechanical properties. The results suggest that by increasing the flexible PTMEG contents from 0% to 60 wt%, the copolymers show decreased glass transition temperatures, melting points, melt-crystallization temperatures, hardness, tensile strength, thermostability, and smaller spherulites dimensions; however it has much increased impact strength and elongation at breaking point. Compared with commercial poly(butylene terephthalate (PBT-type TPEE with 25 mol% flexible segments, PTT-type TPEE having 25 mol% flexible segments has a lower glass transition temperature, melting point, crystallization temperature, and much lower tensile strength although it has a much higher impact strength than that of PBT-type TPEE, and it is not suitably used as a commercial TPEE.

  8. Biopolymer Blends Based on Poly (lactic acid: Shear and Elongation Rheology/Structure/Blowing Process Relationships

    Directory of Open Access Journals (Sweden)

    Racha Al-Itry

    2015-05-01

    Full Text Available This study was dedicated to the blown film extrusion of poly(lactic acid, which mainly presents poor shear and elongation viscosities, and its blends. In order to enhance its melt strength, two main routes were selected (i a structural modification through chain extension and branching mechanisms by adding a reactive multifunctional epoxide (named Joncryl and (ii blending with poly(butylene adipate-co-terephtalate, named PBAT in presence (or not of Joncryl. The effects of the reactive agent on the shear and elongation rheology, morphological, and interfacial properties of the blends were systematically investigated. A decrease of the interfacial tension has been also demonstrated according to the deformed drop retraction method (DDRM. Hence, the role of Joncryl as a compatibilizer was highlighted. Consequently, finer morphology of the dispersed phase was obtained. Furthermore, the impact of the two modification routes on the blown film extrusion ability of PLA has been studied. Based on the improved shear and elongational rheological properties, a great enlargement of the blowing processing window of PLA modified with Joncryl was demonstrated. Indeed, with the addition of Joncryl into PLA–PBAT blends, a reduction of the instability defects has been detected. Finally, the induced crystalline structure and the thermo-mechanical properties of blown films were shown to be improved.

  9. Luminescence-based spectroelectrochemical sensor for [Tc(dmpe)3]2+/+ (dmpe = 1,2-bis(dimethylphosphino)ethane) within a charge-selective polymer film.

    Science.gov (United States)

    Chatterjee, Sayandev; Del Negro, Andrew S; Edwards, Matthew K; Bryan, Samuel A; Kaval, Necati; Pantelic, Nebojsa; Morris, Laura K; Heineman, William R; Seliskar, Carl J

    2011-03-01

    A spectroelectrochemical sensor consisting of an indium tin oxide (ITO) optically transparent electrode (OTE) coated with a thin film of partially sulfonated polystyrene-blockpoly(ethylene-ran-butylene)-block-polystyrene (SSEBS) was developed for [Tc(dmpe)(3)](+) (dmpe = 1,2-bis(dimethylphosphino)ethane). [Tc(dmpe)(3)](+) was preconcentrated by ion-exchange into the SSEBS film after a 20 min exposure to aqueous [Tc(dmpe)(3)](+) solution, resulting in a 14-fold increase in cathodic peak current compared to a bare OTE. Colorless [Tc(dmpe)(3)](+) was reversibly oxidized to colored [Tc(dmpe)(3)](2+) by cyclic voltammetry. Detection of [Tc(dmpe)(3)](2+) was accomplished through emission spectroscopy by electrochemically oxidizing the complex from nonemissive [Tc(dmpe)(3)](+) to emissive [Tc(dmpe)(3)](2+). The working principle of the sensor consisted of electrochemically cycling between nonemissive [Tc(dmpe)(3)](+) and emissive [Tc(dmpe)(3)](2+) and monitoring the modulated emission (λ(exc) = 532 nm; λ(em) = 660 nm). The sensor gave a linear response over the concentration range of 0.16-340.0 μM of [Tc(dmpe)(3)](2+/+) in aqueous phase with a detection limit of 24 nM.

  10. Effects of different level addition of zeolite ZSM-5 additive on quality and composition of the dry gas, LPG (Liquefied Petroleum Gas) and gasoline, produced in FCC (Fluid Catalytic Cracking); Efeito dos diferentes niveis de adicao de aditivos de ZSM-5 na qualidade e composicao do gas combustivel, GLP e gasolina produzidos em FCC

    Energy Technology Data Exchange (ETDEWEB)

    Bastiani, Raquel; Pimenta, Ricardo D.M.; Almeida, Marlon B.B.; Lau, Lam Y. [PETROBRAS S.A., Rio de Janeiro, RJ (Brazil)

    2004-07-01

    The effects of the addition of different level of ZSM-5 additives on different FCC catalysts formulations have been studied on laboratory scale FST (Fluidized Simulation Test). The main objective of the present work is to perform a qualitative identification of the main parameters of FCC catalyst which affect the ZSM-5 additives performance concerning quality and composition of Dry Gas, LPG and Gasoline. The product composition of each test was analyzed by PIANO groups separated by carbon number. The effect of ZSM-5 on products composition was evaluated. The results showed that the ZSM-5 additive cracks gasoline range olefins and isoparaffins into Dry Gas and LPG, favoring the formation of ethylene, propylene and butylenes, while the absolute yield of gasoline aromatics changes little. The aromatics fraction in gasoline, MON and RON numbers in gasoline increase. The ZSM-5 effectiveness is negatively affected by high levels of rare earth on FCC catalyst (RE-USY). Higher hydrogen transfer provides lower olefins (higher than C6) formation, which are the most reactive species for ZSM-5 cracking. (author)

  11. Laser ultrasonic furnace tube coke monitor. Quarterly technical progress report No. 1, May 1--August 1, 1998

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-08-15

    The overall aim of the project is to demonstrate the performance and practical use of a laser ultrasonic probe for measuring the thickness of coke deposits located within the high temperature tubes of a thermal cracking furnace. This aim will be met by constructing an optical probe that will be tested using simulated coke deposits that are positioned inside of a bench-scale furnace. Successful development of the optical coke detector will provide industry with the only available method for on-line measurement of coke deposits. The optical coke detector will have numerous uses in the refining and petrochemical sectors including monitoring of visbreakers, hydrotreaters, delayed coking units, vacuum tower heaters, and various other heavy oil heating applications where coke formation is a problem. The coke detector will particularly benefit the olefins industry where high temperature thermal crackers are used to produce ethylene, propylene, butylene and other important olefin intermediates. The ethylene industry requires development of an on-line method for gauging the thickness of coke deposits in cracking furnaces because the current lack of detailed knowledge of coke deposition profiles introduces the single greatest uncertainty in the simulation and control of modern cracking furnaces. The laser ultrasonic coke detector will provide operators with valuable new information allowing them to better optimize the decoking turnaround schedule and therefore maximize production capacity.

  12. Maximizing light olefins production in fluid catalytic cracking (FCC) units; Maximizacao de olefinas leves em unidades de craqueamento catalitico fluido

    Energy Technology Data Exchange (ETDEWEB)

    Pimenta, Ricardo D.M.; Pinho, Andrea de Rezende [PETROBRAS, Rio de Janeiro, RJ (Brazil)

    2004-07-01

    The Fluid Catalytic Cracking (FCC) process is widely spread over the ten PETROBRAS refineries in its thirteen industrial units. The importance of the FCC process resides on its high gasoline output, being the main supplier of this important product to the system. Additionally, FCC process is the main source of light hydrocarbons in the LPG range, including light olefins. The increasing demand for ethylene, propylene and butylenes was encouraging to concentrate the research efforts on studies about alternatives for the traditional FCC process. In the present work, the proposals from main licensors (UOP, KBR, Stone and Webster) for a light-olefins-driven FCC process (Petrochemical FCC) will be compared. Furthermore, the catalytic route for light olefins production in FCC units is also described. An additive based on ZSM- 5 zeolite, which is produced following a PETROBRAS proprietary technology, is being largely applied into the catalyst inventories of all FCC units. An analysis of different scenarios was performed to estimate the maximum potential of light olefins production from the highest possible ZSM-5 additive usage. More specifically for the case of ethylene, which production is also boosted by the same type of additive, studies are being conducted with the objective of recovering it from a C2 stream using specific units to do the splitting (UPGR). The search for increasing light olefins production in the refining processes is in line with PETROBRAS strategic plan which targeted for the company a more intense activity in the Brazilian petrochemical market (author)

  13. Amphiphilic Beads as Depots for Sustained Drug Release Integrated into Fibrillar Scaffolds

    Science.gov (United States)

    Gaharwar, Akhilesh K.; Mihaila, Silvia M.; Kulkarni, Ashish A.; Patel, Alpesh; Di Luca, Andrea; Reis, Rui L.; Gomes, Manuela E.; van Blitterswijk, Clemens; Moroni, Lorenzo; Khademhosseini, Ali

    2014-01-01

    Native extracellular matrix (ECM) is a complex fibrous structure loaded with bioactive cues that affects the surrounding cells. A promising strategy to mimicking native tissue architecture for tissue engineering applications is to engineer fibrous scaffolds using electrospinning. By loading appropriate bioactive cues within these fibrous scaffolds, various cellular functions such as cell adhesion, proliferation and differentiation can be regulated. Here, we report on the encapsulation and sustained release of model hydrophobic drug (dexamethasone (Dex)) within beaded fibrillar scaffold of poly(ethylene oxide terephthalate)-poly(butylene terephthalate) (PEOT/PBT), a polyether-ester multiblock copolymer to direct differentiation of human mesenchymal stem cells (hMSCs). The amphiphilic beads act as depots for sustained drug release that is integrated into the fibrillar scaffolds. The entrapment of Dex within the beaded structure results in sustained release of drug over the period of 28 days. This is mainly attributed to the diffusion driven release of Dex from the amphiphilic electrospun scaffolds. In vitro results indicate that hMSCs cultured on Dex containing beaded fibrillar scaffolds exhibit an increase in osteogenic differentiation potential, as evidenced by increased alkaline phosphatase (ALP) activity, compared to the direct infusion of Dex in culture medium. The formation of mineralized matrix is also significantly enhanced due to the controlled Dex release from the fibrous scaffolds. This approach can be used to engineer scaffolds with appropriate chemical cues to direct tissue regeneration. PMID:24794894

  14. Development of an active biodegradable film containing tocopherol and avocado peel extract

    Directory of Open Access Journals (Sweden)

    J.C.F. Fidelis

    2015-12-01

    Full Text Available Thermoplastic starch (TPS films and poly(butylene adipate co-terephthalate (PBAT (60/40 m/m containing TOCO-70 (tocopherol/soybean oil 70/30 m/m and avocado peel extract (ExA were produced using blown film extrusion. The formulations of the 5 films (FC/F1/F2/F3 and F4 were established through mixture design with constraints maintaining constant PBAT and TPS proportion, and varying the antioxidant concentrations. Adding antioxidants reduced the water vapour permeability (Kw of the films, with formulation F2 presenting higher decrease in relationto FC, 77.8%. The presence of ExA improved the mechanical properties of the films. The production of the films was determined to be viable after they presented good processability in a pilotextruder, as well as mechanical properties appropriate to production and utilization in industry.The presence of ExA and TOCO 70 provided the films with antioxidant activity; their application as active packaging requires further studies.

  15. Interaction of the organic tin chloride with the liquid model membranes

    Science.gov (United States)

    Podolak, M.; Engel, G.; Man, D.

    2007-08-01

    The objective of the work was to investigate the effect of organic tin chloride (C3H7)3SnCl on the electric parameters of membranes in the form of filters of the company Synpor (Czech Republic) impregnated with various fatty acids, dissolved with carbon tetrachloride (CCl4). Three carboxylic acids were used in the study: palmitic, arachidic and oleic, and dissolvent of the acids (CCl4) as well as butylene ester of lauric acid. In all cases, introduction of tin chloride of constant concentration amounting to 0.15 mM to the measurement chamber resulted in induction of membrane voltage. In case of pure lauric acid and CCl4, the voltage reached the maximum value and then decreased to a certain constant value. In the case of all acids dissolved in CCl4, the voltage increased only up to a certain constant value. Voltage drop (below the value) was observed after application of appropriately high concentration of tin chloride, in case of membranes impregnated with the mixture of lauric acid ester with CCl4 and palmitic acid with CCl4. The study also demonstrated that electrical resistance of membranes impregnated with carboxylic acid increased in the presence of tin chloride and decreased in case of membranes impregnated with lauric acid ester. However, electric capacities of membranes did not significant change.

  16. Interaction of the organic tin chloride with the liquid model membranes

    Energy Technology Data Exchange (ETDEWEB)

    Podolak, M; Engel, G; Man, D [Institute of Physics, Opole University, Oleska 48, 45-052 Opole (Poland)

    2007-08-15

    The objective of the work was to investigate the effect of organic tin chloride (C{sub 3}H{sub 7}){sub 3}SnCl on the electric parameters of membranes in the form of filters of the company Synpor (Czech Republic) impregnated with various fatty acids, dissolved with carbon tetrachloride (CCl{sub 4}). Three carboxylic acids were used in the study: palmitic, arachidic and oleic, and dissolvent of the acids (CCl{sub 4}) as well as butylene ester of lauric acid. In all cases, introduction of tin chloride of constant concentration amounting to 0.15 mM to the measurement chamber resulted in induction of membrane voltage. In case of pure lauric acid and CCl{sub 4}, the voltage reached the maximum value and then decreased to a certain constant value. In the case of all acids dissolved in CCl{sub 4}, the voltage increased only up to a certain constant value. Voltage drop (below the value) was observed after application of appropriately high concentration of tin chloride, in case of membranes impregnated with the mixture of lauric acid ester with CCl{sub 4} and palmitic acid with CCl{sub 4}. The study also demonstrated that electrical resistance of membranes impregnated with carboxylic acid increased in the presence of tin chloride and decreased in case of membranes impregnated with lauric acid ester. However, electric capacities of membranes did not significant change.

  17. Effect of Organic Tin Compounds on Electric Properties of Model Membranes

    Energy Technology Data Exchange (ETDEWEB)

    Podolak, M.; Engel, G.; Man, D. [Inst. of Physics, Opole Univ., Opole (Poland)

    2006-05-15

    The objective of the present work was to investigate the effect of selected organic tin compounds and potassium chloride (used as a reference substance) on the trans-membrane electric voltage and electric resistance of model membranes, the latter being nitrocellulose filters impregnated with butylene ester of lauric acid. The increasing KCl concentration (in the measurement chambers) caused a rapid rise of the negative trans-membrane voltage, whose value stabilized afterwards. In the case of (C{sub 3}H{sub 7}){sub 3}SnCl an abrupt maximum of the negative voltage was observed followed by a monotonic drop to zero. In the case of highest concentrations of this compound the voltages, after having reached zero, changed their polarization to the opposite. Within the range of small concentrations two slight voltage maxima were observed. Non-ionic tin compounds like (CH{sub 3}){sub 4}Sn and (C{sub 2}H{sub 5}){sub 4}Sn had an insignificant influence on the electric properties of the studied membranes. (orig.)

  18. Preparation and characterization of biodegradable aliphatic-aromatic copolyesters/nano-SiO_2 hybrids via in situ melt polycondensation

    Institute of Scientific and Technical Information of China (English)

    Yan Zhang; Bing Tao Wang; Zheng Hong Guo; Jie Chen; Zheng Ping Fang

    2009-01-01

    In situ melt polycondensation was proposed to prepare biodegradable aliphatic-aromatic copolyesters/nano-SiO_2 hybrids based on terephthalic acid (TPA), poly(L-lactic acid) oligomer (OLLA), 1,4-butanediol (BDO) and nano-SiO_2. TEM and FT-IR characterizations confirmed that TPA, OLLA and BDO copolymerized to obtain biodegradable copolyesters, poly(butylene terephthalate-co-lactate) (PBTL), and the abundant hydroxyl groups on the surface of nano-SiO_2 provided potential sites for in situ grafting with the simultaneous resulted PBTL. The nano-SiO_2 particles were chemically wrapped with PBTL to form PBTL/nano-SiO2 hybrids. Due to the good dispersion and interfacial adhesion of nano-SiO_2 particles with the copolyester matrix, the tensile strength and the Young's modulus increased from 5.4 and 5.6 Mpa for neat PBTL to 16 and 390 Mpa for PBTL/nano-SiO_2 hybrids with 5 wt.% nano-SiO_2, respectively. The mechanical properties of PBTL/nano-SiO_2 hybrids were substantially improved.

  19. Towards predicting the solubility of CO2 and N2 in different polymers using a quasi-SMILES based QSPR approach.

    Science.gov (United States)

    Toropov, A A; Toropova, A P; Begum, S; Achary, P G R

    2016-04-01

    The solubility of gases in various polymers plays an important role for the design of new polymeric materials. Quantitative structure-property relationship (QSPR) models were designed to predict the solubility of gases such as CO2 and N2 in polyethylene (PE), polypropylene (PP), polystyrene (PS), polyvinyl acetate (PVA) and poly (butylene succinate) (PBS) at different temperatures and pressures by using quasi-SMILES codes. The dataset of 315 systems was split randomly into training, calibration and validation sets; random split 1 led to 214 training (r(2) = 0.870 and RMSE = 0.019), 51 calibration (r(2) = 0.858 and RMSE = 0.020) and 50 validation (r(2) = 0.869 and RMSE = 0.017) sets. The suggested approach based on the quasi-SMILES, which are analogues of the traditional SMILES gives reasonable good predictions for solubility of CO2 and N2 in different polymers. The described methodology is universal for situations where the aim is to predict the response of an eclectic system upon a variety of physicochemical and/or biochemical conditions. PMID:27097272

  20. The micro thermal analysis of polymers

    CERN Document Server

    Grandy, D B

    2002-01-01

    This study is concerned with the development of micro-thermal analysis as a technique for characterising heterogeneous polymers. It is divided into two main parts. In the first part, the use of miniature Wollaston wire near-field thermal probes mounted in an atomic force microscope (AFM) to carry out highly localised thermal analysis (L-TA) of amorphous and semi-crystalline polymers is investigated. Here, the temperature of the probe sensor or tip is scanned over a pre-selected temperature range while in contact with the surface of a sample. It is thereby used to heat a volume of material of the order of several cubic micrometres. The effect of the glass transition, cold crystallisation, melting and degree of crystallinity on L-TA measurements is investigated. The materials used are poly(ethylene terephthalate), polystyrene and fluorocarbon-coated poly(butylene terephthalate). The primary measurements are the micro- or localised analogues of thermomechanical analysis (L-TMA) and differential thermal analysis ...

  1. Purification and Properties of an Extracellular Polyhydroxybutyrate Depolymerase from Pseudomonas mendocina DSWY0601

    Institute of Scientific and Technical Information of China (English)

    WANG Yan; LI Fan; WANG Zhan-yong; LIU Dong-bo; XIA Hong-mei; LIU Ling-fei; CHEN Shan

    2012-01-01

    An extracellular polyhydroxybutyrate(PHB) depolymerase was purified to homogeneity from the culture supematant of a PHB-degrading bacterium,Pseudomonas mendocina DSWY0601,which was isolated from brewery sewage for the ability to form clear zones on the PHB mineral agar plates.The molecular weight of the purified PHB depolymerase as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis(SDS-PAGE) was approximately 59800 at the optimal temperature and pH value being 50℃ and 8.5,respectively.PHB depolymerase was stable in a temperature rangc of 20--50℃ and sensitive to pH value within a pH range of 8.0--9.5.PHB depolymerase degraded poly-3-hydroxybutyrate-co-4-hydroxybutyrate(P3/4HB) and poly-3-hydroxybutyrate-co-3-hydroxyvalerate(PHBV) but did not degrade poly(lactic acid)(PLA),poly(butylene succinate)(PBS) or poly(caprolactone)(PCL).PHB depolymerase was sensitive to phenylmethylsulfonyl fluoride(PMSF),H2O2 and SDS.The main product after enzymatic degradation of PHB was indentified as 3-hydroxbutyrate monomer(3HB) by mass spectrometric analysis,suggesting that PHB depolymerase acted as an exo-type hydrolase.Analysis ofphaZpm gene reveals that PHB depolymerase is a typical denatured short-chain-length PHA(dPHAscL,PHA=polyhydroxyalkanoate)depolymerase containing catalytic domain,linker and substrate-binding domain.

  2. Droplet immobilization within a polymeric organogel improves lipid bilayer durability and portability.

    Science.gov (United States)

    Venkatesan, Guru A; Sarles, Stephen A

    2016-05-24

    The droplet interface bilayer (DIB) is a promising technique for assembling lipid membrane-based materials and devices using water droplets in oil, but it has largely been limited to laboratory environments due to its liquid construction. With a vision to transform this lab-based technique into a more-durable embodiment, we investigate the use of a polymer-based organogel to encapsulate DIBs within a more-solid material matrix to improve their handling and portability. Specifically, a temperature-sensitive organogel formed from hexadecane and poly[styrene-b-(ethylene-co-butylene)-b-styrene] (SEBS) triblock copolymer is used to replace the liquid solvent that surrounds the lipid-coated droplets to establish a novel liquid-in-gel DIB system. Through specific capacitance measurements and single-channel recordings of the pore forming peptide alamethicin, we verify that the structural and functional membrane properties are retained when DIBs are assembled within SEBS organogel. In addition, we demonstrate that organogel encapsulation offers improved handling of droplets and yields DIBs with a near 3× higher bilayer durability, as quantified by the lateral acceleration required to rupture the membrane, compared to liquid-in-liquid DIBs in oil. This encapsulated DIB system provides a barrier against contamination from the environment and offers a new material platform for supporting multilayered DIB-based devices as well as other digital microfluidic systems that feature water droplets in oil. PMID:27164314

  3. Starch/polyester films: simultaneous optimisation of the properties for the production of biodegradable plastic bags

    Directory of Open Access Journals (Sweden)

    J. B. Olivato

    2013-01-01

    Full Text Available Blends of starch/polyester have been of great interest in the development of biodegradable packaging. A method based on multiple responses optimisation (Desirability was used to evaluate the properties of tensile strength, perforation force, elongation and seal strength of cassava starch/poly(butylene adipate-co-terephthalate (PBAT blown films produced via a one-step reactive extrusion using tartaric acid (TA as a compatibiliser. Maximum results for all the properties were set as more desirable, with an optimal formulation being obtained which contained (55:45 starch/PBAT (88.2 wt. (%, glycerol (11.0 wt. (% and TA (0.8 wt. (%. Biodegradable plastic bags were produced using the film with this formulation, and analysed according to the standard method of the Associação Brasileira de Normas Técnicas (ABNT. The bags exhibited a 45% failure rate in free-falling dart impact tests, a 10% of failure rate in dynamic load tests and no failure in static load tests. These results meet the specifications set by the standard. Thus, the biodegradable plastic bags fabricated with an optimised formulation could be useful as an alternative to those made from non-biodegradable materials if the nominal capacity declared for this material is considered.

  4. Novel High Performance Ziegler-Natta Catalyst for Ethylene Slurry Polymerization%新型高性能Ziegler-Natta催化剂用于乙烯淤浆聚合

    Institute of Scientific and Technical Information of China (English)

    郭子芳; 陈伟; 周俊领; 杨红旭

    2009-01-01

    A novel high performance MgCl2/TiCl4 catalyst with tetrabutyloxsilicane as electron donor was pre-pared for ethylene slurry polymerization process. The properties of the catalyst such as particle size distribution, catalytic activity, hydrogen responsibility and copolymerization performance were investigated and compared with commercial catalyst (imported catalyst). Copolymerization of ethylene and 1-butylene using the catalyst was stud-ied in a pilot plant. The composition, structure and property of the copolymer were characterized by 13C nuclear magnetic resonance (13C NMR) and gel permeation chromatography-Infrared (GPC-IR), and compared with those of the copolymer obtained from a commercial catalyst. In comparison with the commercial catalyst, the novel cata-lyst had a higher activity (up to 34.6 kg·g-1) and a better particle size distribution (PSD), and produced polymers having higher bulk density (up to 0.37 g·cm-3) with less fine resin. Meanwhile, the novel catalyst showed a higher hydrogen r sponsibility and better copolymerization performance. The results indicated that the copolymer obtained from the novel catalyst has a higher branch in the high molecular weight fraction and lower branch in the low mo-lecular weight fraction.

  5. Effects of mercaptans and disulfides on photochemical and high energy radiation induced reactions. Progress report, November 1, 1974--October 31, 1975

    International Nuclear Information System (INIS)

    A chain reaction may be formulated at alkaline pH in terms of e-/sub aq/ acting as a source of -OH as a reactant and H. regenerating e-/sub aq/. This may account for radiolytic conversion of CO to formate with high G. 60Co γ-radiolysis of alkaline aqueous acetonitrile and acetamide gave no evidence of a chain; extensive hydrolysis of methyl acetate is now attributed to non-radiolytic, normal hydrolysis. Aromatic mercaptans are found to retard photoreduction of a benzophenone by aliphatic amines, largely by hydrogen atom-transfer repair reactions. Aliphatic mercaptans accelerate photoreduction, apparently by affecting the reduction to quenching ratio in the intermediate charge-transfer complex. In photoreduction of a benzophenone by 2,3-butylene glycol at pH 3, the glycol is converted, not to 3-hydroxy-2-butanone, but to 2-butanone, and about 4 molecules of this are formed per molecule of ketone reduced. A short chain appears to be established. Mercaptan appears to accelerate the reduction of the ketone and retard the formation of 2-butanone

  6. Effect of reinforcement nanoparticles addition on mechanical properties of SBS/curaua fiber composites

    Energy Technology Data Exchange (ETDEWEB)

    Borba, Patricia M. [Servico Nacional de Aprendizagem Industrial (CETEPO/SENAI/RS), Sao Leopoldo, RS (Brazil). Centro Tecnologico de Polimeros; Tedesco, Adriana [Braskem S. A., III Polo Petroquimico, Triunfo, RS (Brazil); Lenz, Denise M., E-mail: denise.lenz@gmail.com [Universidade Luterana do Brasil (ULBRA), Canoas, RS (Brazil). Programa de Pos-graduacao em Engenharia de Materiais e Processos Sustentaveis

    2014-03-15

    Composites of styrene-butadiene-styrene triblock copolymer (SBS) matrix with curauá fiber and/or a nanoparticulated mineral (montmorillonite clay - MMT) used as reinforcing agents were prepared by melt-mixing. The influence of clay addition on properties like tensile and tear strength, rebound resilience, flex fatigue life, abrasion loss, hardness and water absorption of composites with 5, 10 and 20 wt% of curauá fiber was evaluated in presence of maleic anhydride grafted styrene-(ethylene-co-butylene)-styrene triblock copolymer (MA-g-SEBS) coupling agent. Furthermore, the effect of mineral plasticizer loading on tensile strength of selected composites was investigated. The hybrid SBS composite that showed the best overall mechanical performance was composed by 2 wt% of MMT and 5 wt% of curauá fiber. Increasing fiber content up to 20 wt% resulted in a general decrease in all mechanical properties as well as incorporation of 5 wt% MMT caused a decrease in the tensile strength in all fiber contents. The hybrid composites showed clay agglomerates (tactoids) poorly dispersed that could explain the poor mechanical performance of composites at higher concentrations of curauá fiber and MMT nanoparticles. The addition of plasticizer further decreased the tensile strength while the addition of MMT nanoparticles decreased water absorption for all SBS composites. (author)

  7. Binary Mixed Homopolymer Brushes Tethered to Cellulose Nanocrystals: A Step Towards Compatibilized Polyester Blends.

    Science.gov (United States)

    Mincheva, Rosica; Jasmani, Latifah; Josse, Thomas; Paint, Yoann; Raquez, Jena-Marie; Gerbaux, Pascal; Eyley, Samuel; Thielemans, Wim; Dubois, Philippe

    2016-09-12

    This article reports on the successful preparation and characterization of cellulose nanocrystals (CNCs) surface-modified with polylactide (PLA) and poly(butylene succinate) (PBS) binary mixed homopolymer brushes. Their synthesis was designed as a three-step procedure combining polyester synthesis and surface-modification of CNCs with simultaneous polyester grafting via a heterogeneous copper(I)-catalyzed azide-alkyne cycloaddition reaction. For comparison, single homopolymer brushes tethered to CNCs (PLLA-g-CNC and PBSBDEMPAM-g-CNC) were obtained applying the same procedure. The hairy nanoparticles were characterized in terms of chemical composition and thermal properties. Spectroscopic analyses suggested "rippled" microphase separation of both immiscible homopolyesters in the mixed brushes, while others showed impeded homopolyester crystallization after surface-grafting. A synergistic relationship between the polyesters and CNCs was also suggested, i.e., the polyester grafting increases the CNC thermal resistance, while CNC presence imparts char formation. The as-obtained binary homopolymer brushes tethered to nanoparticles makes these surface-modified cellulosic nanomaterials attractive as compatibilization/reinforcement agents for PLA/PBS blends.

  8. An open source image processing method to quantitatively assess tissue growth after non-invasive magnetic resonance imaging in human bone marrow stromal cell seeded 3D polymeric scaffolds.

    Directory of Open Access Journals (Sweden)

    Anne M Leferink

    Full Text Available Monitoring extracellular matrix (ECM components is one of the key methods used to determine tissue quality in three-dimensional (3D scaffolds for regenerative medicine and clinical purposes. This is even more important when multipotent human bone marrow stromal cells (hMSCs are used, as it could offer a method to understand in real time the dynamics of stromal cell differentiation and eventually steer it into the desired lineage. Magnetic Resonance Imaging (MRI is a promising tool to overcome the challenge of a limited transparency in opaque 3D scaffolds. Technical limitations of MRI involve non-uniform background intensity leading to fluctuating background signals and therewith complicating quantifications on the retrieved images. We present a post-imaging processing sequence that is able to correct for this non-uniform background intensity. To test the processing sequence we investigated the use of MRI for in vitro monitoring of tissue growth in three-dimensional poly(ethylene oxide terephthalate-poly(butylene terephthalate (PEOT/PBT scaffolds. Results showed that MRI, without the need to use contrast agents, is a promising non-invasive tool to quantitatively monitor ECM production and cell distribution during in vitro culture in 3D porous tissue engineered constructs.

  9. Gamma Irradiation of Polyesters Film

    International Nuclear Information System (INIS)

    Experimental investigations on the effects of gamma irradiation in air of aromatic polyesters are carried out, in order to evaluate the influence of aromatic density and the role of oxygen on the radiation resistance. The thermoplastic polyesters PolyEthyleneTerephthalate (PET), PolyButylene Terephthalate (PBT), PolyEthyleneNaphthalate (PEN), Poly1,4-cyclohexanedimethylen terephthalate-co-ethyleneterephthalate (PCT-co-ET) are moulded in thin films of 50 micron and irradiated at different absorbed doses, ranging from 0 to 1000 kGy, using a Co-60 gamma source. The structural changes in the polymers are studied by means of several physical-chemical and nuclear techniques. Electron Paramagnetic Resonance analyses are carried out to detect the radicals induced by irradiation and to follow their decay by oxygen permeation. Viscometric measurements show a similar trend for the different irradiated polyesters: in particular, chain scission induced by irradiation depends on the aromatic density contained in the polymer and shows a saturation effect at the highest doses. Positron Annihilation Lifetime Spectroscopy points out a decrease of the ortho-positronium signal caused by the production of oxidized species inhibiting the positronium formation. Finally, the experimental results obtained on the irradiated films are compared with previous studies carried out on the same polyesters moulded in sheets of 1-2 mm of thickness and γ-irradiated at the same adsorbed doses

  10. Structure and properties of SEBS/PP/OMMT nanocomposites

    Institute of Scientific and Technical Information of China (English)

    WANG Xia; PANG Shao-long; YANG Jun-he; YANG Fan

    2006-01-01

    Nanocomposites based on styrene-b-(ethylene-co-butylenes)-b-styrene triblock copolymer(SEBS),polypropylene (PP) and organomontmorillonite (OMMT) were prepared using melt intercalation by a twin mill. The nanostructure of SEBS/PP/OMMT hybrids was characterized by X-ray diffractometry(XRD) and transmission electron microscopy(TEM). The d001 space of OMMT and SEBS/PP/OMMT hybrid increases from 1.30 nm to 3.52 nm and 4.06 nm,respectively which indicate,that the C16 and SEBS/PP could intercalate in the silicate layers and expand the basal spacing. The formation of intercalated structure was also confirmed by TEM. The results show that the individual silicates are well dispersed in the elastomer matrix. The glass transition temperature (tg) of PS block of SEBS was investigated by dynamic mechanical analysis (DMA). It is shown that there are remarkable enhancements in tg of PS block containing a small mass fraction of OMMT. tg of PS in SEBS of the nanocomposites has been increased about 39 ℃ when containing 4% OMMT. The influence of OMMT on the dynamic storage moduli is temperature dependent. Below 50 ℃ the SEBS/PP/OMMT composites with higher OMMT contents show higher dynamic storage moduli. OMMT has the function of reinforcing SEBS/PP elastomers. However,the influence of OMMT on the mechanical properties of the nanocomposites is not significant according to the tensile test and tear test.

  11. Influence of Flame Retardants on the Melt Dripping Behaviour of Thermoplastic Polymers

    Directory of Open Access Journals (Sweden)

    Melissa Matzen

    2015-08-01

    Full Text Available Melt flow and dripping of the pyrolysing polymer melt can be both a benefit and a detriment during a fire. In several small-scale fire tests addressing the ignition of a defined specimen with a small ignition source, well-adjusted melt flow and dripping are usually beneficial to pass the test. The presence of flame retardants often changes the melt viscosity crucially. The influence of certain flame retardants on the dripping behaviour of four commercial polymers, poly(butylene terephthalate (PBT, polypropylene (PP, polypropylene modified with ethylene-propylene rubber (PP-EP and polyamide 6 (PA 6, is analysed based on an experimental monitoring of the mass loss due to melt dripping, drop size and drop temperature as a function of the furnace temperature applied to a rod-shaped specimen. Investigating the thermal transition (DSC, thermal and thermo-oxidative decomposition, as well as the viscosity of the polymer and collected drops completes the investigation. Different mechanisms of the flame retardants are associated with their influence on the dripping behaviour in the UL 94 test. Reduction in decomposition temperature and changed viscosity play a major role. A flow limit in flame-retarded PBT, enhanced decomposition of flame-retarded PP and PP-EP and the promotion of dripping in PA 6 are the salient features discussed.

  12. Study of cerium-promoted rhodium alumina catalyst as a steam reforming catalyst for treatment of spent solvents

    Institute of Scientific and Technical Information of China (English)

    Hee-Chul Yang; Min-Woo Lee; Ho-Sang Hwang; Jei-Kwon Moon; Dong-Yong Chung

    2014-01-01

    This study attempted to develop an appropriate catalyst used for the steam reforming of gasified spent solvents. Rh2O3/ CeO2-Al2O3 catalysts with various CeO2 loadings were prepared and heated at different temperatures of 500 and 800 ºC, and their surface properties were studied using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron mi-croscopy (TEM), temperature programmed reduction (TPR) and Brumauer-Emmett-Teller (BET) analyses. Rhodium existed in the form of Rh2O3, regardless of the sample composition as well as the heating temperature. In the tested range of cerium addition (up to 12 times the rhodium mass), no significant changes in BET surface areas and binding energy corresponding to Rh 3d5/2were observed. Instead, the addition of cerium led to a greatly enhanced dispersion of rhodium nanoparticles, and no agglomeration of rhodium was observed for samples heated even at 800 ºC. Honeycomb monolith rhodium catalysts promoted with cerium were fabricated and tested for the steam reforming of a gasified spent solvent, mainly consisting of butylene (C4H8). The test results suggested that a ce-rium-promoted rhodium catalyst could be used as an appropriate reforming catalyst for treating low-quality non-methane hydrocar-bons without the formation of coke at high temperatures of up to 900 ºC.

  13. CO2-Philic polymer membrane with extremely high separation performance

    KAUST Repository

    Yave, Wilfredo

    2010-01-12

    Polymeric membranes are attractive for CO2 separation and concentration from different gas streams because of their versatility and energy efficiency; they can compete with, and they may even replace, traditional absorption processes. Here we describe a simple and powerful method for developing nanostructured and CO2-philic polymer membranes for CO2 separation. A poly(ethylene oxide)-poly(butylene terephthalate) multiblock copolymer is used as membrane material. Smart additives such as polyethylene glycol dibutyl ether are incorporated as spacers or fillers for producing nanostructured materials. The addition of these specific additives produces CO2-philic membranes and increases the CO2 permeability (750 barrer) up to five-fold without the loss of selectivity. The membranes present outstanding performance for CO2 separation, and the measured CO2 flux is extremely high ( > 2 m3 m -2 h-1 bar-1) with selectivity over H2 and N2 of 10 and 40, respectively, making them attractive for CO 2 capture. © 2009 American Chemical Society.

  14. Application of polymer nanocomposites in the nanomedicine landscape: envisaging strategies to combat implant associated infections.

    Science.gov (United States)

    Dwivedi, Poushpi; Narvi, Shahid S; Tewari, Ravi P

    2013-01-01

    This review article presents an overview of the potential biomedical application of polymer nanocomposites arising from different chemistries, compositions, and constructions. The interaction between the chosen matrix and the filler is of critical importance. The existing polymer used in the biomedical arena includes aliphatic polyesters such as polylactide (PLA), poly(ε-caprolactone) (PCL), poly(p-dioxanone) (PPDO), poly(butylenes succinate) (PBS), poly(hydroxyalkanoate)s, and natural biopolymers such as starch, cellulose, chitin, chitosan, lignin, and proteins. The nanosized fillers utilized to fabricate the nanocomposites are inorganic, organic, and metal particles such as clays, magnetites, hydroxyapatite, nanotubes chitin whiskers, lignin, cellulose, Au, Ag, Cu, etc. These nanomaterials are taking root in a variety of diverse healthcare applications in the sector of nanomedicine including the domain of medical implants and devices. Despite sterilization and aseptic procedures the use of these biomedical devices and prosthesis to improve the patient's 'quality of life' is facing a major impediment because of bacterial colonization causing nosocomial infection, together with the multi-drug-resistant 'super-bugs' posing a serious threat to its utility. This paper discusses the current efforts and key research challenges in the development of self-sterilizing nanocomposite biomaterials for potential application in this area. PMID:24127037

  15. Identification and Comparative Quantification of Bio-Active Phthalides in Essential Oils from Si-Wu-Tang, Fo-Shou-San, Radix Angelica and Rhizoma Chuanxiong

    Directory of Open Access Journals (Sweden)

    Yin Lu

    2010-01-01

    Full Text Available Phthalides are important bio-active constituents in Si-Wu-Tang and Fo-Shou-San, two commonly used Traditional Chinese Medicine (TCM combined prescriptions mainly derived from Radix Angelica and Rhizoma Chuanxiong. In this paper, the contents of eight phthalides, including Z-ligustilide, E-ligustilide, Z-butylenephthalide, E-butylene-phthalide, 3-butylphthalide, neocnidilide and senkyunolide A were determined or estimated by gas chromatography–mass spectrometry (GC-MS. The results showed GC-MS was a simple, rapid, and high sensitive method for analyzing phthalides in Si-Wu-Tang, Fo-Shou-San, Radix Angelica and Rhizoma Chuanxiong, and the extractable contents of each phthalides including Z-ligustilide, E-ligustilide, Z-butylenephthalide, etc. varied after Radix Angelica, Rhizoma Chuanxiong were combined into a formulation, such as Si-Wu-Tang and Fo-Shou-San. Furthermore, inhibition activity of essential oils from Si-Wu-Tang, Fo-Shou-San, Radix Angelica and Rhizoma Chuanxiong on uterine contraction was tested in an in vitro assay, and the results showed that the activity of the essential oil is higher as the content of the phthalides increase, which demonstrated that phthalides are possibly main active components inhibiting mice uterine contraction in vitro. All of the results suggested that comparative analysis of chemical components and pharmacological activities of each herb and formula is possibly helpful to elucidate the active components in traditional Chinese medicine, and to reveal the compatibility mechanism of TCM formulae.

  16. MISCIBILITY, CRYSTALLIZATION AND MECHANICAL PROPERTIES OF PPC/PBS BLENDS

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    In this paper, melt blends of poly(propylene carbonate) (PPC) with poly(butylene succinate) (PBS) were characterized by dynamic mechanical analysis (DMA), differential scanning calorimetry (DSC), tensile testing, wide-angle X-ray diffraction (WAXD), polarized optical microscopy and thermogravimetric analysis (TGA). The results indicated that the glass transition temperature of PPC in the 90/10 PPC/PBS blend was decreased by about 11 K comparing with that of pure PPC. The presence of 10% PBS was partially miscible with PPC. The 90/10 PPC/PBS blend had better impact and tensile strength than those of the other PPC/PBS blends. The glass transition temperature of PPC in the 80/20, 70/30, and 60/40 PPC/PBS blends was improved by about 4.9 K, 4.2 K, and 13 K comparing with that of pure PPC, respectively; which indicated the immiscibility between PPC and PBS. The DSC results indicated that the crystallization of PBS became more difficult when the PPC content increased. The matrix of PPC hindered the crystallization process of PBS. While the content of PBS was above 20%, significant crystallization-induced phase separation was observed by polarized optical microscopy.It was found from the WAXD analysis that the crystal structure of PBS did not change, and the degree of crystallinity increased with increasing PBS content in the PPC/PBS blends.

  17. Mechanical and thermal properties of PP/PBT blends compatibilized with triblock thermoplastic elastomer

    Directory of Open Access Journals (Sweden)

    Ignaczak Wojciech

    2015-09-01

    Full Text Available A linear triblock copolymer, poly(styrene-b-etylene/butylene-b-styrene(SEBS thermoplastic elastomer (TPE grafted with maleic anhydride was used for compatibilization of PP/PBT blends. PP/PBT blends of different mass ratios 60/40, 50/50, 40/60 were mixed with 2.5, 5.0 and 7.5 wt.% of SEBS copolymer in a twin screw extruder. Differential scanning calorimetry and dynamic mechanical analysis were performed to define the phase structure of PP/PBT blends. TPE with a rubbery mid-block shifted the glass transition of PP/PBT blend towards lower temperatures, and significant decrease the crystallization temperature of a crystalline phase of PP component was observed. The influence of the amount of compatibilizer and the blend composition on the mechanical properties (tensile and flexural strengths, toughness and moduli was determined. Addition of 5 wt.% of a triblock TPE led to a three-fold increase of PP/PBT toughness. A significant increase of impact properties was observed for all materials compatibilized with the highest amount of SEBS copolymer.

  18. Synthesis and characterization of biodegradable aliphatic copolyesters with hydrophilic soft segments

    Directory of Open Access Journals (Sweden)

    JASNA DJONLAGIC

    2004-12-01

    Full Text Available In this study, the synthesis, structure and physical properties of two series of segmented poly(ester-ethers based on poly(butylene succinate and two different types of polyethers were investigated. The poly(ester-ethers were synthesized by transesterification reaction of dimethyl succinate, 1,4-butanediol and poly(ethylene oxide (PEO, Mn = 1000 g/mol in the first series, and poly(tetramethylene oxide (PTMO, Mn = 1000 g/mol in the second. The mass fraction of soft segments was varied between 10 and 50 mass. %. The effect of the introduction of two different polyether soft segments on the structure, thermal and rheological properties were investigated. The composition of the poly(ester-ethers, determined from their 1H-NMR spectra, showed that incorporation of soft polyether segments was successfully performed by the transesterification reaction in bulk. The molecular weight was estimated from solution viscosity measurements and complex dynamic viscosities. The thermal properties investigated by DSC indicated that the presence of soft segments lowers the melting and crystallization temperature of the hard phase, as well as the degree of crystallinity. Dynamical mechanical analysis was used to investigate the influence of composition on the rheological behavior of the segmented poly(ester-ethers. The results obtained from an enzymatic degradation test performed on some of the synthesized polymers showed that the biodegradability is enhanced with increasing hydrophilicity.

  19. [The determination of glucose, sucrose and fructose by the method of capillary electrophoresis].

    Science.gov (United States)

    Yakuba, Yu F; Markovsky, M G

    2015-01-01

    The possibilities of different regimes of micellar capillary electrophoresis using negative polarity and alkaline electrolyte for determination of glucose, sucrose, fructose in extracts of vegetative organs of plants and products of fruits and grapes processing have been studied. A comparative evaluation of the limits of detection of glucose, sucrose, fructose for developed electrolytes have been performed, the advantages and disadvantages of techniques have been discussed. It is recommended to use an aqueous electrolyte containing 0.5% potassium sorbate, 0.62% cetyltrimethylammonium bromide, and 0.02% potassium hydroxide. The analyzed components were detected at 254 nm. The sample was dosed hydrodynamically (30 mbar, 5 sec). Negative voltage 16 kV is recommended, current--54 ± 4 µA, capillary thermostating at 24 °C is applied, the analysis time--15 min. The detection limits for fructose and glucose is 0.03 g/dm3 to 0.07 g of sucrose/dm3. Linearity is stored for each component to 5.0 g/dm 3 inclusive. Electrophoretic mobility of carbohydrates was (10(-4) sm2V(-1)sec(-1)): fructose--3.12, glucose--3.03, sucrose--2.74. Approximate time of release: glucose--13 min, sucrose--13.5 min, fructose--12.5 min. The developed options for mass concentration determining of mono- and disaccharides provide complete separation of the components. Anions, glycerol, ethylene glycol, propylene glycol and butylene isomers do not affect the analysis results. PMID:26402948

  20. Significant Enhancement of Mechanical and Thermal Properties of Thermoplastic Polyester Elastomer by Polymer Blending and Nanoinclusion

    Directory of Open Access Journals (Sweden)

    Manwar Hussain

    2016-01-01

    Full Text Available Thermoplastic elastomer composites and nanocomposites were fabricated via melt processing technique by blending thermoplastic elastomer (TPEE with poly(butylene terephthalate (PBT thermoplastic and also by adding small amount of organo modified nanoclay and/or polytetrafluoroethylene (PTFE. We study the effect of polymer blending on the mechanical and thermal properties of TPEE blends with and without nanoparticle additions. Significant improvement was observed by blending only TPEE and virgin PBT polymers. With a small amount (0.5 wt.% of nanoclay or PTFE particles added to the TPEE composite, there was further improvement in both the mechanical and thermal properties. To study mechanical properties, flexural strength (FS, flexural modulus (FM, tensile strength (TS, and tensile elongation (TE were all investigated. Thermogravimetric analysis (TGA and differential scanning calorimetry (DSC were used to analyze the thermal properties, including the heat distortion temperature (HDT, of the composites. Scanning electron microscopy (SEM was used to observe the polymer fracture surface morphology. The dispersion of the clay and PTFE nanoparticles was confirmed by transmission electron microscopy (TEM analysis. This material is proposed for use as a baffle plate in the automotive industry, where both high HDT and high modulus are essential.

  1. Hybrid organotin and tin oxide-based thin films processed from alkynylorganotins: synthesis, characterization, and gas sensing properties.

    Science.gov (United States)

    Renard, Laetitia; Brötz, Joachim; Fuess, Hartmut; Gurlo, Aleksander; Riedel, Ralf; Toupance, Thierry

    2014-10-01

    Hydrolysis-condensation of bis(triprop-1-ynylstannyl)butylene led to nanostructured bridged polystannoxane films yielding tin dioxide thin layers upon UV-treatment or annealing in air. According to Fourier transform infrared (FTIR) spectroscopy, contact angle measurements, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and scanning electron microscopy (SEM) data, the films were composed of a network of aggregated "pseudo-particles", as calcination at 600 °C is required to form cassiterite nanocrystalline SnO2 particles. In the presence of reductive gases such as H2 and CO, these films gave rise to highly sensitive, reversible, and reproducible responses. The best selectivity toward H2 was reached at 150 °C with the hybrid thin films that do not show any response to CO at 20-200 °C. On the other hand, the SnO2 films prepared at 600 °C are more sensitive to H2 than to CO with best operating temperature in the 300-350 °C range. This organometallic approach provides an entirely new class of gas-sensing materials based on a class II organic-inorganic hybrid layer, along with a new way to include organic functionality in gas sensing metal oxides.

  2. Phase morphological study on SEBS compatibilized PS/LDPE blends

    Directory of Open Access Journals (Sweden)

    Chatchai Kunyawut

    2014-09-01

    Full Text Available The co-continuous phase morphology of polystyrene (PS/low density polyethylene (LDPE blends compatibilized with poly(styrene-block-ethylene/butylene-block-styrene triblock copolymers (SEBS with varying molecular weights has been investigated. The blend samples were prepared in a mini-twin screw extruder. The barrel length and diameter are 224 and 16 mm, respectively. The diameter of the capillary die is 1 mm. The concentration of the blends was 70/30 wt% of PS/LDPE while that of the SEBS used was 5 wt% of the blend. The mixing temperatures used were 180, 250, and 280o C, and a screw speed of 60 rpm. The morphology of the blends was investigated using an AFM technique. Average droplet diameters of the blend samples were determined using an OM technique. The co-continuous morphology has not been obtained in all the blends, although the mixing temperature used is as high as 280o C. The experimental results indicated that the model prediction of the co-continuous morphology proposed by Willemse and co-worker was not applicable to the blend systems studied. Only droplet-type dispersion was observed. This is considered to arise from the processing conditions and the mixing device used. The blend compatibilized with the high molecular weight SEBS had higher dispersed phase size than that of the blend compatibilized with the medium and low molecular weight SEBSs. This behaviour is likely to arise from coalescence during melt processing.

  3. A Facile Strategy to Fabricate Multishape Memory Polymers with Controllable Mechanical Properties.

    Science.gov (United States)

    Zhang, Qinglong; Hua, Wenqiang; Feng, Jiachun

    2016-08-01

    A facile blending strategy to fabricate multishape memory polymers (SMPs) with only one sort of phase transition material has been reported. In this work, olefin block copolymer (OBC) and styrene-b-(ethylene-co-butylene)-b-styrene (SEBS), which are both physically crosslinked, are blended with crystalline paraffin together. Due to the different interactions between polymer matrices and paraffin, the paraffin penetrated in OBC and SEBS exhibit separated melting transitions. It is quite interesting that merely paraffin distributed in OBC also shows two distinct melting transitions with enough OBC content in composites. Therefore, excellent quadruple shape memory effect can be achieved with a maximum of three melting transitions. Furthermore, through adjusting the polymer species and content, the mechanical and rheological properties can be conveniently tuned to a great extent. Compared with the reported strategies, this simple and controllable method sheds light on rapid design of multi-SMPs using inexpensive raw materials, which greatly paves the way for multi-SMPs from laboratory to factory.

  4. BLEND MEMBRANES FOR DIRECT METHANOL AND PROTON EXCHANGE MEMBRANE FUEL CELLS

    Institute of Scientific and Technical Information of China (English)

    Perurnal Bhavani; Dharmalingam Sangeetha

    2012-01-01

    Sulphonated polystyrene ethylene butylene polystyrene (SPSEBS) prepared with 35% sulphonation was found to be highly elastic and enlarged up to 300%-400% of its initial length.It absorbed over 110% of water by weight.A major drawback of this membrane is its poor mechanical properties which are not adequate for use as polymer electrolytes in fuel cells.To overcome this,SPSEBS was blended with poly(vinylidene fluoride) (PVDF),a hydrophobic polymer.The blend membranes showed better mechanical properties than the base polymer.The effect of PVDF content on water uptake,ion exchange capacity and proton conductivity of the blend membranes was investigated.This paper presents the results of recent studies applied to develop an optimized in-house membrane electrode assembly (MEA) preparation technique combining catalyst ink spraying and assembly hot pressing.Easy steps were chosen in this preparation technique in order to simplify the method,aiming at cost reduction.The open circuit voltage for the cell with SPSEBS is 0.980 V which is higher compared to that of the cell with Nafion 117 (0.790 V).From this study,it is concluded that a polymer electrolyte membrane suitable for proton exchange membrane fuel cell (PEMFC) and direct methanol fuel cell (DMFC) application can be obtained by blending SPSEBS and PVDF in appropriate proportions.The methanol permeability and selectivity showed a strong influence on DMFC performance.

  5. Study and development of nanocomposites PBT/bentonite clay treated by ionizing radiation: preparation and characterization

    International Nuclear Information System (INIS)

    This work describes the preparation and characterization of composites based on poly (butylene terephthalate) - PBT and brazilian modified clay prepared by the melt intercalation. PBT nanocomposites with 3 and 5 % by weight of organically modified clay, by the addition of a quaternary ammonium salt, were prepared by extrusion using a twin-screw extruder machine. After the extrusion process, the materials were injected to obtain specimens tests samples for the characterization tests. Part of the specimens samples were irradiated using an electron beam accelerator with 1.5 MeV at room temperature in the presence of air. Samples of pure PBT and irradiated and non-irradiated nanocomposites were characterized by mechanical tests of tensile, flexural and impact, heat distortion temperature (HDT), X - ray diffraction (XRD), scanning electron microscopy (SEM), melt flow index (MFI) thermogravimetry (TG) and differential scanning calorimetry (DSC) and the correlation between the properties was discussed. The results showed that the addition of clay, in both percentages, promoted an increase greater than 50 % in tensile strength at break and a gain of around 35% in heat distortion temperature when compared to the pure polymer. The treatment with ionizing radiation of electron beam at the doses used in this study showed no significant changes in material properties. (author)

  6. Preparation and Characterization of Polycarbonate Modified Multiple-walled Carbon Nanotubes

    Institute of Scientific and Technical Information of China (English)

    YU Jin-Gang; HUANG Ke-Long; LIU Su-Qin; TANG Jin-Chun

    2008-01-01

    To prepare polymer/carbon nanotube composites, polycarbonate was chosen to modify multiple-walled carbon nanotubes. Poly[(propylene oxide)-(carbon dioxide)-(ε-caprolactone)], poly(butylene-co-ε-caprolactone carbonate),and poly[(propylene oxide)-co-(carbon dioxide)-co-(maleic anhydride)] were the polycarbonates which were used to modify multiple-walled carbon nanotubes, but only soluble poly[(propylene oxide)-(carbon dioxide)-(ε-caprolactone)] modified multiple-walled carbon nanotubes could be obtained. Thermogravimetric analysis clearly indicated that more polycarbonates were attached to soluble poly[(propylene oxide)-(carbon dioxide)-(ε-caprolactone)] modified multiple-walled carbon nanotubes. The formation of surface functional groups and changes of nanotube structures and morphology were monitored by infrared spectroscopy, scanning electron microscopy and transmission electron microscopy, respectively. Because of their solubility and bioactive moieties,poly[(propylene oxide)-(carbon dioxide)-(ε-caprolactone)] modified multiple-walled carbon nanotubes may find their potential use in drug delivery.

  7. Functional groups grafted nonwoven fabrics for blood filtration-The effects of functional groups and wettability on the adhesion of leukocyte and platelet

    Energy Technology Data Exchange (ETDEWEB)

    Yang Chao [State Key Lab of Metal Matrix Composites, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240 (China); Cao Ye [Institute of Blood Transfusion, Chinese Academy of Medical Sciences and Peking Union Medical College, Chengdu 610081 (China); Sun Kang, E-mail: ksun@sjtu.edu.cn [State Key Lab of Metal Matrix Composites, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240 (China); Liu Jiaxin; Wang Hong [Institute of Blood Transfusion, Chinese Academy of Medical Sciences and Peking Union Medical College, Chengdu 610081 (China)

    2011-01-15

    In this work, the effects of grafted functional groups and surface wettability on the adhesion of leukocyte and platelet were investigated by the method of blood filtration. The filter materials, poly(butylene terephthalate) nonwoven fabrics bearing different functional groups including hydroxyl (OH), carboxyl (COOH), sulfonic acid group (SO{sub 3}H) and zwitterionic sulfobetaine group ({sup +}N((CH{sub 3}){sub 2})(CH{sub 2}){sub 3}SO{sub 3}{sup Circled-Minus }) with controllable wettability were prepared by UV radiation grafting vinyl monomers with these functional groups. Our results emphasized that both surface functional groups and surface wettability had significant effects on the adhesion of leukocyte and platelet. In the case of filter materials with the same wettability, leukocytes adhering to filter materials decreased in the order: the surface bearing OH only > the surface bearing both OH and COOH > the surface bearing sulfobetaine group > the surface bearing SO{sub 3}H, while platelets adhering to filter materials decreased as the following order: the surface bearing SO{sub 3}H > the surface bearing both OH and COOH > the surface bearing OH only > the surface bearing sulfobetaine group. As the wettability of filter materials increased, both leukocyte and platelet adhesion to filter materials declined, except that leukocyte adhesion to the surface bearing OH only remained unchanged.

  8. Biodegradable compounds: Rheological, mechanical and thermal properties

    Science.gov (United States)

    Nobile, Maria Rossella; Lucia, G.; Santella, M.; Malinconico, M.; Cerruti, P.; Pantani, R.

    2015-12-01

    Recently great attention from industry has been focused on biodegradable polyesters derived from renewable resources. In particular, PLA has attracted great interest due to its high strength and high modulus and a good biocompatibility, however its brittleness and low heat distortion temperature (HDT) restrict its wide application. On the other hand, Poly(butylene succinate) (PBS) is a biodegradable polymer with a low tensile modulus but characterized by a high flexibility, excellent impact strength, good thermal and chemical resistance. In this work the two aliphatic biodegradable polyesters PBS and PLA were selected with the aim to obtain a biodegradable material for the industry of plastic cups and plates. PBS was also blended with a thermoplastic starch. Talc was also added to the compounds because of its low cost and its effectiveness in increasing the modulus and the HDT of polymers. The compounds were obtained by melt compounding in a single screw extruder and the rheological, mechanical and thermal properties were investigated. The properties of the two compounds were compared and it was found that the values of the tensile modulus and elongation at break measured for the PBS/PLA/Talc compound make it interesting for the production of disposable plates and cups. In terms of thermal resistance the compounds have HDTs high enough to contain hot food or beverages. The PLA/PBS/Talc compound can be, then, considered as biodegradable substitute for polystyrene for the production of disposable plates and cups for hot food and beverages.

  9. Reduction of Noise from Disc Brake Systems Using Composite Friction Materials Containing Thermoplastic Elastomers (TPEs)

    Science.gov (United States)

    Masoomi, Mohsen; Katbab, Ali Asghar; Nazockdast, Hossein

    2006-09-01

    Attempts have been made for the first time to prepare a friction material with the characteristic of thermal sensitive modulus, by the inclusion of thermoplastic elastomers (TPE) as viscoelastic polymeric materials into the formulation in order to the increase the damping behavior of the cured friction material. Styrene butadiene styrene (SBS), styrene ethylene butylene styrene (SEBS) and nitrile rubber/polyvinyl chloride (NBR/PVC) blend system were used as TPE materials. In order to evaluate the viscoelastic parameters such as loss factor (tan δ) and storage modulus (E‧) for the friction material, dynamic mechanical analyzer (DMA) were used. Natural frequencies and mode shapes of friction material and brake disc were determined by modal analysis. However, NBR/PVC and SEBS were found to be much more effective in damping behavior. The results from this comparative study suggest that the damping characteristics of commercial friction materials can be strongly affected by the TPE ingredients. This investigation also confirmed that the specimens with high TPE content had low noise propensity.

  10. Fabrication and characterization of thermoplastic elastomer dry adhesives with high strength and low contamination.

    Science.gov (United States)

    Bin Khaled, Walid; Sameoto, Dan

    2014-05-14

    Polydimethylsiloxane (PDMS) and polyurethane elastomers have commonly been used to manufacture mushroom shaped gecko-inspired dry adhesives with high normal adhesion strength. However, the thermosetting nature of these two materials severely limits the commercial viability of their manufacturing due to long curing times and high material costs. In this work, we introduce poly(styrene-ethylene/butylene-styrene) (SEBS) thermoplastic elastomers as an alternative for the manufacture of mushroom shaped dry adhesives with both directional and nondirectional performance. These materials are attractive for their potential to be less contaminating via oligomer transfer than thermoset elastomers, as well as being more suited to mass manufacturing. Low material transfer properties are attractive for adhesives that could potentially be used in cleanroom environments for microscale assembly and handling in which device contamination is a serious concern. We characterized a thermoplastic elastomer in terms of oligomer transfer using X-ray photoelectron spectroscopy and found that the SEBS transfers negligible amounts of its own oligomers, during contact with a gold-coated silicon surface, which may be representative of the metallic bond pads found in micro-electro-mechanical systems devices. We also demonstrate the fabrication of mushroom shaped isotropic and anisotropic adhesive fibers with two different SEBS elastomer grades using thermocompression molding and characterize the adhesives in terms of their shear-enhanced normal adhesion strength. The overall adhesion of one of the thermoplastic elastomer adhesives was found to be stronger or comparable to their polyurethane counterparts with identical dimensions.

  11. Laser-induced breakdown spectroscopy for polymer identification.

    Science.gov (United States)

    Grégoire, Sylvain; Boudinet, Marjorie; Pelascini, Frédéric; Surma, Fabrice; Detalle, Vincent; Holl, Yves

    2011-07-01

    This study aims at differentiating several organic materials, particularly polymers, by laser induced breakdown spectroscopy. The goal is to apply this technique to the fields of polymer recycling and cultural heritage conservation. We worked with some usual polymers families: polyethylene (PE), polypropylene (PP), polyoxymethylene, (POM), poly(vinyl chloride), polytetrafluoroethylene, polyoxyethylene (POE), and polyamide for the aliphatic ones, and poly(butylene terephthalate), acrylonitrile-butadiene-styrene, polystyrene, and polycarbonate for the aromatic ones. The fourth harmonic of a Nd:YAG laser (266 nm) in ambient air at atmospheric pressure was used. A careful analysis of the C(2) Swan system (0,0) band in polymers containing no C-C (POM), few C-C (POE), or aromatic C-C linkages led us to the conclusion that the C(2) signal might be native, i.e., the result of direct ablation from the sample. With use of these results, aliphatic and aromatic polymers could be differentiated. Further data treatments, such as properly chosen line ratios, principal component analysis, and partial least squares regression, were evaluated. It was shown that many polymers could be separated, including PE and PP, despite their similar chemical structures.

  12. Microwell scaffolds for the extrahepatic transplantation of islets of Langerhans.

    Directory of Open Access Journals (Sweden)

    Mijke Buitinga

    Full Text Available Allogeneic islet transplantation into the liver has the potential to restore normoglycemia in patients with type 1 diabetes. However, the suboptimal microenvironment for islets in the liver is likely to be involved in the progressive islet dysfunction that is often observed post-transplantation. This study validates a novel microwell scaffold platform to be used for the extrahepatic transplantation of islet of Langerhans. Scaffolds were fabricated from either a thin polymer film or an electrospun mesh of poly(ethylene oxide terephthalate-poly(butylene terephthalate (PEOT/PBT block copolymer (composition: 4000PEOT30PBT70 and were imprinted with microwells, ∼400 µm in diameter and ∼350 µm in depth. The water contact angle and water uptake were 39±2° and 52.1±4.0 wt%, respectively. The glucose flux through electrospun scaffolds was three times higher than for thin film scaffolds, indicating enhanced nutrient diffusion. Human islets cultured in microwell scaffolds for seven days showed insulin release and insulin content comparable to those of free-floating control islets. Islet morphology and insulin and glucagon expression were maintained during culture in the microwell scaffolds. Our results indicate that the microwell scaffold platform prevents islet aggregation by confinement of individual islets in separate microwells, preserves the islet's native rounded morphology, and provides a protective environment without impairing islet functionality, making it a promising platform for use in extrahepatic islet transplantation.

  13. Fluorinated Amphiphilic Polymers and Their Blends for Fouling-Release Applications: The Benefits of a Triblock Copolymer Surface

    KAUST Repository

    Sundaram, Harihara S.

    2011-09-28

    Surface active triblock copolymers (SABC) with mixed polyethylene glycol (PEG) and two different semifluorinated alcohol side chains, one longer than the other, were blended with a soft thermoplastic elastomer (TPE), polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SEBS). The surface composition of these blends was probed by X-ray photoelectron spectroscopy (XPS) and near edge X-ray absorption fine structure (NEXAFS) spectroscopy. The surface reconstruction of the coatings in water was monitored qualitatively by dynamic water contact angles in air as well as air bubble contact angle measurements in water. By blending the SABC with SEBS, we minimize the amount of the SABC used while achieving a surface that is not greatly different in composition from the pure SABC. The 15 wt % blends of the SABC with long fluoroalkyl side chains showed a composition close to that of the pure SABC while the SABC with shorter perfluoroakyl side chains did not. These differences in surface composition were reflected in the fouling-release performance of the blends for the algae, Ulva and Navicula. © 2011 American Chemical Society.

  14. Enhancement of Biodegradable Plastic-degrading Enzyme Production from Paraphoma-like Fungus, Strain B47-9.

    Science.gov (United States)

    Sameshima-Yamashita, Yuka; Koitabashi, Motoo; Tsuchiya, Wataru; Suzuki, Ken; Watanabe, Takashi; Shinozaki, Yukiko; Yamamoto-Tamura, Kimiko; Yamazaki, Toshimasa; Kitamoto, Hiroko

    2016-01-01

    To improve the productivity of Paraphoma-like fungal strain B47-9 for biodegradable plastic (BP)-degrading enzyme (PCLE), the optimal concentration of emulsified poly(butylene succinate-co-adipate) (PBSA) in the medium was determined. Emulsified PBSA was consumed as a sole carbon source and an inducer of PCLE production by strain B47-9. Among the various concentrations of emulsified PBSA [0.09-0.9% (w/v)] used in flask cultivation, 0.27% yielded the maximum enzyme activity within a short cultivation period. To evaluate the residual concentration of emulsified PBSA in culture, emulsified PBSA in aliquots of culture supernatant was digested in vitro, and the concentration of released monomerised succinic acid was determined. Regardless of the initial concentration of emulsified PBSA in medium, PCLE activity was detected after residual succinic acid decreased below 0.04 mg/mL in culture broth. Jarfermentation was performed at a 0.27% PBSA concentration. Among the various airflow rates tested, 1 LPM resulted in a PCLE production rate of 1.0 U/mL/day. The enzyme activity in the resulting culture filtrate (4.2 U/2 mL) was shown to degrade commercial BP films (1 × 1 cm, 20 µm thickness) within 8 hours. PMID:26876678

  15. Electron beam damage in high temperature polymers

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, S. (Dayton Univ., OH (USA). Research Inst.); Adams, W.W. (Air Force Materials Lab., Wright-Patterson AFB, OH (USA))

    1990-01-01

    Electron microscopic studies of polymers are limited due to beam damage. Two concerns are the damage mechanism in a particular material, and the maximum dose for a material before damage effects are observed. From the knowledge of the dose required for damage to the polymer structure, optimum parameters for electron microscopy imaging can be determined. In the present study, electron beam damage of polymers has been quantified by monitoring changes in the diffraction intensity as a function of electron dose. The beam damage characteristics of the following polymers were studied: poly(p-phenylene benzobisthiazole) (PBZT); poly(p-phenylene benzobisoxazole) (PBO); poly(benzoxazole) (ABPBO); poly(benzimidazole) (ABPBI); poly(p-phenylene terephthalamide) (PPTA); and poly(aryl ether ether ketone) (PEEK). Previously published literature results on polyethylene (PE), polyoxymethylene (POM), nylon-6, poly(ethylene oxide) (PEO), PBZT, PPTA, PPX, iPS, poly(butylene terephthalate) (PBT), and poly(phenylene sulphide) (PPS) were reviewed. This study demonstrates the strong dependence of the electron beam resistivity of a polymer on its thermal stability/melt temperature. (author).

  16. Performance and environmental impact of biodegradable polymers as agricultural mulching films.

    Science.gov (United States)

    Touchaleaume, François; Martin-Closas, Lluís; Angellier-Coussy, Hélène; Chevillard, Anne; Cesar, Guy; Gontard, Nathalie; Gastaldi, Emmanuelle

    2016-02-01

    In the aim of resolving environmental key issues such as irreversible soil pollution by non-biodegradable and non-recoverable polyethylene (PE) fragments, a full-scale field experiment was set up to evaluate the suitability of four biodegradable materials based on poly(butylene adipate-co-terephtalate) (PBAT) to be used as sustainable alternatives to PE for mulching application in vineyard. Initial ultimate tensile properties, functional properties during field ageing (water vapour permeability and radiometric properties), biodegradability and agronomical performance of the mulched vines (wood production and fruiting yield) were studied. In spite of their early loss of physical integrity that occurred only five months after vine planting, the four materials satisfied all the requested functional properties and led to agronomic performance as high as polyethylene. In the light of the obtained results, the mulching material lifespan was questioned in the case of long-term perennial crop such as grapevine. Taking into account their mulching efficiency and biodegradability, the four PBAT-based studied materials are proven to constitute suitable alternatives to the excessively resistant PE material. PMID:26386433

  17. Modification of Biodegradable Polyesters Using Electron Beam

    International Nuclear Information System (INIS)

    Poly(4-Hydroxybutyrate) P4HB, Poly(butylene succinate-co-adipate) PBSA and Poly(ε-caprolactone) PCL were electron beam (EB)-irradiated. Poly(4-Hydroxybutyrate) was irradiated without any polyfunctional monomers (PFM). While PBSA and PCL were irradiated in the presence of polyfunctional monomers such as Trimethallyl isocyanurate (TMAIC), Polyethyleneglycol dimethacrylate (2G, 4G), Trimethylolpropane trimethacrylate (TMPT) and Tetramethylolmethane tetraacrylate (A-TMMT) at ambient temperature. Aim of the study is to improve the properties of biodegradable polyester. It was pointed out that crosslinking yield of P4HB (6.39% gel) was formed at dose of 90 kGy irradiated in vacuum conditions. Radiation degradation promoted, when P4HB was irradiated in air. The optimum crosslinking yield of PCL and PBSA respectively, were formed in the presence of 1% TMAIC at dose of 50 kGy. The biodegradability of the crosslinked PBSA evaluated by soil burial test is slightly retarded by increasing crosslinking yields. (author)

  18. Radiation crosslinking of polymer materials and its functional properties

    International Nuclear Information System (INIS)

    It was found out that radiation crosslinking of biodegradable polymer such as poly (butylene succinate, PBS) and poly(ε-caprolactone, PCL) could be achieved by radiation in the presence of small amount of trimethallyl isocyanurate (TMAIC) or 1% triallyl isocyanurate (TAIC). Such modification is very effective to improve heat resistance for PBS and PCL. Poly (lactic acid, PLA) undergoes crosslinking effectively with 3% TAIC by radiation. Outstanding feature of these polymers is their biodegradability even after crosslinking. Radiation crosslinking of polysaccharide derivatives such as carboxymethyl-cellulose (CMC) is also achieved in aqueous solution at high concentration (paste-like state). The crosslinking behavior was largely affected by the degree of substitution (DS) and polymer concentration. After removal of water the dry CMC gel is used as water absorbent material. This dry gel is the most effective for removal of large amounts of water from organic wastes, resulting in the acceleration of their fermentation. Measurement of swelling ratio of the dry CMC gel in 0.9% NaCl aqueous solution was carried out to expand application fields for this material. Radiation crosslinked poly (vinyl alcohol) hydrogel was successfully commercialized from July 2004 as wound dressing for accelerated healing. Furthermore, this material was also used as gel protector to prevent shore sore and was further commercialized. (author)

  19. Performance and environmental impact of biodegradable polymers as agricultural mulching films.

    Science.gov (United States)

    Touchaleaume, François; Martin-Closas, Lluís; Angellier-Coussy, Hélène; Chevillard, Anne; Cesar, Guy; Gontard, Nathalie; Gastaldi, Emmanuelle

    2016-02-01

    In the aim of resolving environmental key issues such as irreversible soil pollution by non-biodegradable and non-recoverable polyethylene (PE) fragments, a full-scale field experiment was set up to evaluate the suitability of four biodegradable materials based on poly(butylene adipate-co-terephtalate) (PBAT) to be used as sustainable alternatives to PE for mulching application in vineyard. Initial ultimate tensile properties, functional properties during field ageing (water vapour permeability and radiometric properties), biodegradability and agronomical performance of the mulched vines (wood production and fruiting yield) were studied. In spite of their early loss of physical integrity that occurred only five months after vine planting, the four materials satisfied all the requested functional properties and led to agronomic performance as high as polyethylene. In the light of the obtained results, the mulching material lifespan was questioned in the case of long-term perennial crop such as grapevine. Taking into account their mulching efficiency and biodegradability, the four PBAT-based studied materials are proven to constitute suitable alternatives to the excessively resistant PE material.

  20. Phase diagrams in blends of poly(3-hydroxybutyric acid with various aliphatic polyesters

    Directory of Open Access Journals (Sweden)

    2011-07-01

    Full Text Available Phase behavior with immiscibility, miscibility, crystalline morphology, and kinetic analysis in blends of poly(3-hydroxybutyric acid (PHB with aliphatic polyesters such as poly(butylene adipate (PBA, poly(ethylene adipate (PEA, poly(trimethylene adipate (PTA, or poly(ethylene succinate (PESu, respectively, were explored mainly using differential scanning calorimeter (DSC and polarized-light optical microscopy (POM. Immiscibility phase behavior with reversible upper-critical-solution-temperature (UCST is common in the PHB/polyester blends. The polyester/polyester blend of PHB/PTA is partially miscible with no UCST in melt and amorphous glassy states within a composition range of PTA less than 50 wt%. The miscible crystalline/crystalline blend exhibits ring-banded spherulites at Tc = 50~100°C, with inter-ring spacing dependent on Tc. All immiscible or partially miscible PHB/polyester blends, by contrast, exhibit disrupted ringbanded spherulites or discrete spherical phase domains upon cooling from UCST to crystallization. The blends of PHB with all other aliphatic polyesters, such as PESu, PEA, PBA, etc. are only partially miscible or immiscible with an upper critical solution temperature (UCST at 180~221°C depending on blend composition. UCST with reversibility was verified.

  1. Study and development of nanocomposites PBT/bentonite clay treated by ionizing radiation: preparation and characterization; Estudo e desenvolvimento de nanocompositos PBT/argila bentonita tratados por radiacao ionizante: preparacao e caracterizacao

    Energy Technology Data Exchange (ETDEWEB)

    Sartori, Mariana do Nascimento

    2014-07-01

    This work describes the preparation and characterization of composites based on poly (butylene terephthalate) - PBT and brazilian modified clay prepared by the melt intercalation. PBT nanocomposites with 3 and 5 % by weight of organically modified clay, by the addition of a quaternary ammonium salt, were prepared by extrusion using a twin-screw extruder machine. After the extrusion process, the materials were injected to obtain specimens tests samples for the characterization tests. Part of the specimens samples were irradiated using an electron beam accelerator with 1.5 MeV at room temperature in the presence of air. Samples of pure PBT and irradiated and non-irradiated nanocomposites were characterized by mechanical tests of tensile, flexural and impact, heat distortion temperature (HDT), X - ray diffraction (XRD), scanning electron microscopy (SEM), melt flow index (MFI) thermogravimetry (TG) and differential scanning calorimetry (DSC) and the correlation between the properties was discussed. The results showed that the addition of clay, in both percentages, promoted an increase greater than 50 % in tensile strength at break and a gain of around 35% in heat distortion temperature when compared to the pure polymer. The treatment with ionizing radiation of electron beam at the doses used in this study showed no significant changes in material properties. (author)

  2. Assessing a Spectroelectrochemical Sensor's Performance for Detecting [Ru(bpy)3]2+ in Natural and Treated Water

    Energy Technology Data Exchange (ETDEWEB)

    Abu, Eme A.; Bryan, Samuel A.; Seliskar, Carl J.; Heineman, William R.

    2012-07-01

    A spectroelectrochemical sensor that combines three modes of selectivity in a single device was evaluated in natural and treated water samples using tris-(2,2’-bipyridyl) ruthenium(II) dichloride hexahydrate, [Ru(bpy)3]2+, as a model analyte. The sensor was an optically transparent indium tin oxide (ITO) electrode coated with a thin film of partially sulfonated polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SSEBS). As the potential of the ITO electrode was cycled from +0.7 to +1.3 V, the analyte changed from the colored [Ru(bpy)3]2+ complex to colorless [Ru(bpy)3]3+ complex and the change in absorbance at 450 nm was used as the optical signal for quantification. Calibration curves were obtained for [Ru(bpy)3]2+ in natural well water, river water and treated tap water with detection limits of 108, 139 and 264 nM, respectively. A standard addition method was developed to determine an *unknown* spike addition concentration of [Ru(bpy)3]2+ in well water. The spectroelectrochemical sensor determined the concentration of [Ru(bpy)3]2+ spiked into a sample of Hanford well water to be 0.39*0.03 mM versus the actual concentration of 0.40 mM.

  3. Surfactant-modified nickel zinc iron oxide/polymer nanocomposites for radio frequency applications

    International Nuclear Information System (INIS)

    Low loss, flexible, polymer nanocomposites with improved magneto-dielectric properties at radio frequencies (RF) were successfully fabricated. Surfactant-modified nickel zinc iron oxide (NiZnFe2O4) nanoparticles with ferrimagnetic behavior at room temperature were synthesized by a seed-mediated growth method. The surfactant prevented NiZnFe2O4 particle aggregation and provided compatibility with [styrene-b-ethylene/butylene-b-styrene] block copolymer matrices. NiZnFe2O4/polymer composites were prepared by a solution-casting method. Experimental results showed that the dielectric permittivity (εr) and magnetic permeability (μr) of the polymer composite increased with increasing amount of NiZnFe2O4 doping. The dielectric loss (tanδ) was less than 0.010 at 1 GHz frequency. The increased miniaturization factor ((εrμr)1/2) and relative wave impedance ((μr/εr)1/2) of the NiZnFe2O4 nanocomposites could potentially lead to a reduced RF device's physical size with ease in impedance matching. Dynamic mechanical analysis (DMA) revealed that nanocomposites maintained 125% strain (elongation at break) with 30% nanoparticle doping.

  4. FADS2 function loss at the cancer hotspot 11q13 locus diverts lipid signaling precursor synthesis to unusual eicosanoid fatty acids.

    Directory of Open Access Journals (Sweden)

    Woo Jung Park

    Full Text Available BACKGROUND: Genes coding for the fatty acid desaturases (FADS1, 2, 3 localized at the cancer genomic hotspot 11q13 locus are required for the biosynthesis of 20 carbon polyunsaturated fatty acids (PUFA that are direct eicosanoid precursors. In several cancer cell lines, FADS2 encoded Δ6 and Δ8 desaturation is not functional. METHODOLOGY/PRINCIPAL FINDINGS: Analyzing MCF7 cell fatty acids with detailed structural mass spectrometry, we show that in the absence of FADS2 activity, the FADS1 product Δ5-desaturase operates to produce 5,11,14-20∶3 and 5,11,14,17-20∶4. These PUFA are missing the 8-9 double bond of the eicosanoid signaling precursors arachidonic acid (5,8,11,14-20∶4 and eicosapentaenoic acid (5,8,11,14,17-20∶5. Heterologous expression of FADS2 restores Δ6 and Δ8-desaturase activity and normal eicosanoid precursor synthesis. CONCLUSIONS/SIGNIFICANCE: The loss of FADS2-encoded activities in cancer cells shuts down normal PUFA biosynthesis, deleting the endogenous supply of eicosanoid and downstream docosanoid precursors, and replacing them with unusual butylene-interrupted fatty acids. If recapitulated in vivo, the normal eicosanoid and docosanoid cell signaling milieu would be depleted and altered due to reduction and substitution of normal substrates with unusual substrates, with unpredictable consequences for cellular communication.

  5. Study on the Synthesis Process and Performance Comparison of Aliphatic Polyester%脂肪族聚酯的合成工艺及性能比较研究∗

    Institute of Scientific and Technical Information of China (English)

    寇莹; 郭鹏; 陈红亮

    2015-01-01

    In this paper,for the poly butylene succinate,succinic acid glycol ester,succinic acid glycol ester/top adipic acid glycol ester copolymer,PLA and PCL aliphatic polyester,the synthesis process and properties of them were compared. By comparing the relationship between synthesis and material properties of aliphatic polyester,for the synthesis and modification to provide train of thought.%对聚丁二酸丁二醇酯、聚丁二酸乙二醇酯、聚丁二酸己二醇酯/己二酸己二醇酯共聚物、聚乳酸以及聚己内酯等脂肪族聚酯的合成工艺及性能进行比较,通过比较探讨合成工艺和材料性能之间的关系,得出力学性能和分子量,性能和结晶度以及降解性之间的关系,为脂肪族聚酯的合成改性及降解研究提供思路。

  6. Gelatin-Modified Polyurethanes for Soft Tissue Scaffold

    Directory of Open Access Journals (Sweden)

    Justyna Kucińska-Lipka

    2013-01-01

    Full Text Available Recently, in the field of biomaterials for soft tissue scaffolds, the interest of their modification with natural polymersis growing. Synthetic polymers are often tough, and many of them do not possess fine biocompatibility. On the other hand, natural polymers are biocompatible but weak when used alone. The combination of natural and synthetic polymers gives the suitable properties for tissue engineering requirements. In our study, we modified gelatin synthetic polyurethanes prepared from polyester poly(ethylene-butylene adipate (PEBA, aliphatic 1,6-hexamethylene diisocyanate (HDI, and two different chain extenders 1,4-butanediol (BDO or 1-ethoxy-2-(2-hydroxyethoxyethanol (EHEE. From a chemical point of view, we replaced expensive components for building PU, such as 2,6-diisocyanato methyl caproate (LDI and 1,4-diisocyanatobutane (BDI, with cost-effective HDI. The gelatin was added in situ (in the first step of synthesis to polyurethane to increase biocompatibility and biodegradability of the obtained material. It appeared that the obtained gelatin-modified PU foams, in which chain extender was BDO, had enhanced interactions with media and their hydrolytic degradation profile was also improved for tissue engineering application. Furthermore, the gelatin introduction had positive impact on gelatin-modified PU foams by increasing their hemocompatibility.

  7. Synthesis of thermoplastic poly(ester-siloxanes in the melt and in solution

    Directory of Open Access Journals (Sweden)

    BILJANA P. DOJCINOVIC

    2005-12-01

    Full Text Available Two series of thermoplastic elastomers, based on poly(dimethylsiloxane, PDMS, as the soft segment and poly(butylene terephthalate, PBT, as the hard segment, were synthesized by catalyzed transesterification, from dimethyl terephthalate, DMT, silanol-terminated poly(dimethylsiloxane, PDMS-OH, Mn = 1750 g/mol, and 1,4-butanediol, BD. The mole ratio of the starting comonomers was selected to result in a constant hard to soft weight ratio of 55:45. The first series was synthesized in order to determine the optimal mole ratio of BD and DMT for the synthesis of high molecular weight thermoplastic poly(ester-siloxanes, TPESs. The second series was performed in the presence of the high-boiling solvent, 1,2,4-trichlorbenzene in order to increase the mixing between the extremely non-polar siloxane prepolymer and the polar reactants, DMT and BD, and, therefore, avoid phase separation during synthesis. The structure and composition of the synthesized poly(ester- siloxanes were verified by 1H-NMR spectroscopy, while the melting temperatures and degree of crystallinity were determined by differential scanning calorimetry (DSC. The effectiveness of the incorporation of the silanol-terminated poly( dimethylsiloxane into the polyester chains was verified by chloroform extraction. The rheological properties of the poly(ester-siloxanes were investigated by dynamic mechanical spectroscopy (DMA.

  8. Synthesis, structure and properties of thermoplastic poly(ester–siloxane elastomers

    Directory of Open Access Journals (Sweden)

    VESNA V. ANTIC

    2006-07-01

    Full Text Available Two series of thermoplastic poly(ester–siloxane elastomers (TPES, with hard segments based on poly(butylene terephthalate (PBT and soft segments based on poly(dimethylsiloxane (PDMS, were synthesized by high-temperature, two-step transesterification reaction in the melt. In series I, themass ratio of hard and soft segments was kept constant (57:43, while the length of the segments was varied, whereas in series II, the mass ratio of hard and soft segments was varied in range from 70:30 to 40:60, with a constant length of the soft segments. The segmented structure of the poly(ester–siloxane copolymers was verified by 1H-NMR spectroscopy of the soluble and insoluble fractions, obtained after extraction of the samples with chloroform. The influence of the structure and composition of the TPES on the melting temperatures and degrees of crystallinity was investigated by differential scanning calorimetry (DSC. The rheological properties were investigated by dynamic mechanical analysis (DMA.

  9. Application of polymer nanocomposites in the nanomedicine landscape: envisaging strategies to combat implant associated infections.

    Science.gov (United States)

    Dwivedi, Poushpi; Narvi, Shahid S; Tewari, Ravi P

    2013-12-16

    This review article presents an overview of the potential biomedical application of polymer nanocomposites arising from different chemistries, compositions, and constructions. The interaction between the chosen matrix and the filler is of critical importance. The existing polymer used in the biomedical arena includes aliphatic polyesters such as polylactide (PLA), poly(ε-caprolactone) (PCL), poly(p-dioxanone) (PPDO), poly(butylenes succinate) (PBS), poly(hydroxyalkanoate)s, and natural biopolymers such as starch, cellulose, chitin, chitosan, lignin, and proteins. The nanosized fillers utilized to fabricate the nanocomposites are inorganic, organic, and metal particles such as clays, magnetites, hydroxyapatite, nanotubes chitin whiskers, lignin, cellulose, Au, Ag, Cu, etc. These nanomaterials are taking root in a variety of diverse healthcare applications in the sector of nanomedicine including the domain of medical implants and devices. Despite sterilization and aseptic procedures the use of these biomedical devices and prosthesis to improve the patient's 'quality of life' is facing a major impediment because of bacterial colonization causing nosocomial infection, together with the multi-drug-resistant 'super-bugs' posing a serious threat to its utility. This paper discusses the current efforts and key research challenges in the development of self-sterilizing nanocomposite biomaterials for potential application in this area.

  10. Mechanical and dielectric properties of SEBS modified by graphite inclusion and composite interface

    Science.gov (United States)

    Grigorescu, Ramona Marina; Ciuprina, Florin; Ghioca, Paul; Ghiurea, Marius; Iancu, Lorena; Spurcaciu, Bogdan; Panaitescu, Denis Mihaela

    2016-02-01

    Tough and flexible dielectrics were prepared using graphite (G), a natural and low-cost resource, as filler in polystyrene-b-(ethylene-co-butylene)-b-polystyrene (SEBS) and maleinized SEBS (SEBS-MA) matrices. The disintegration of graphite in submicron particles was accomplished by the shear forces during the melt processing step and it was highlighted by atomic force microscopy. Simultaneous increase of tensile strain, strength and Young's modulus was noticed for SEBS/G and SEBS-MA/G composites compared to unfilled matrices, this remarkable feature being previously reported only for some nanocomposites. Moreover, an exponential variation of the dielectric permittivity with the volume fraction of G was obtained. Higher reinforcing efficiency and better dielectric properties were observed in SEBS-MA/G composites, compared to the corresponding SEBS/G composites, due to the stronger polymer-filler interface and better dispersion of graphite. This study brings new insights into nanolevel properties of SEBS composites and it opens new perspectives on high performance composites by using graphite instead of expensive graphene and efficient melt mixing process.

  11. X-ray scattering studies of ordered block copolymer melts during uniaxial extensional flow

    Science.gov (United States)

    Burghardt, Wesley; Mao, Ruinan; McCready, Erica

    2012-02-01

    We present the design and implementation of a new apparatus for in situ x-ray scattering studies of polymer melts during homogenous uniaxial extensional flow. The instrument is based on the commercial SER extensional flow fixture, which employs counter-rotating drums to deform a strip of polymer melt, which is incorporated into a custom-built convection oven designed to facilitate x-ray access to the sample and operation in a synchrotron environment. Here we report measurements of extensional flow-induced structural changes in a cylindrically ordered styrene-ethylene butylene-styrene triblock copolymer melt. At early stages, SAXS data reveal that the ordered microstructure deforms affinely until Hencky strains of ˜ 0.2. A global re-orientation process leads to alignment of microdomains predominantly along the stretching direction after Hencky strains of ˜ 1. Further stretching does not lead to further qualitative changes in 2-D SAXS patterns. Relaxation of both microdomain orientation and d-spacing is observed following cessation of extensional flow, albeit with different characteristic time scales. In situ x-ray scattering data are compared with off-line measurements of transient extensional viscosity, performed using the SER fixture in a rotational rheometer.

  12. Association behavior of mixed triblock copoly(oxyalkylene)s (type EBE and ESE) in aqueous solution.

    Science.gov (United States)

    Ricardo, Nágila M P S; Chaibundit, Chiraphon; Yang, Zhuo; Attwood, David; Booth, Colin

    2006-01-31

    The micellization of binary mixtures of water-soluble block copolymers E(m)B(n)E(m) and E(m)S(n)E(m) in dilute solution was investigated by light-scattering methods. We use the notation E, B, and S to denote chain units derived, respectively, from ethylene oxide, butylene oxide, and styrene oxide and the subscripts to denote number-average chain lengths in chain units. Two distinct distributions of micelles were formed in solutions of a 50:50 wt % mixture of copolymers E64B20E64 and E137S18E137, which had hydrophobic blocks of similar length but very different hydrophobicity. One distribution of micelles was formed in solutions of a mixture (50:50 wt %) of copolymers E135B20E135 and E82S9E82, which had hydrophobic blocks of different length but similar hydrophobicity. In this case, the properties of the micelles formed in solutions of the mixture were very similar to those of micelles of E82S9E82 alone. This result extended to concentrated solutions, because the hard-gel boundary for the mixture proved to be very similar to that of solutions of E82S9E82 alone.

  13. Study of Syngas Conversion to Light Olefins by Response Surface Methodology

    Directory of Open Access Journals (Sweden)

    Hossein Atashi

    2013-01-01

    Full Text Available The effect of adding MgO to a precipitated iron-cobalt-manganese based Fischer-Tropsch synthesis (FTS catalyst was investigated via response surface methodology. The catalytic performance of the catalysts was examined in a fixed bed microreactor at a total pressure of 1–7 bar, temperature of 280–380°C, MgO content of 5–25% and using a syngas having a H2 to CO ratio equal to 2.The dependence of the activity and product distribution on MgO content, temperature, and pressure was successfully correlated via full quadratic second-order polynomial equations. The statistical analysis and response surface demonstrations indicated that MgO significantly influences the CO conversion and chain growth probability as well as ethane, propane, propylene, butylene selectivity, and alkene/alkane ratio. A strong interaction between variables was also evidenced in some cases. The decreasing effect of pressure on alkene to alkane ratio is investigated through olefin readsorption effects and CO hydrogenation kinetics. Finally, a multiobjective optimization procedure was employed to calculate the best amount of MgO content in different reactor conditions.

  14. Engineering Biodegradable Flame Retardant Wood-Plastic Composites

    Science.gov (United States)

    Zhang, Linxi

    Wood-plastic composites (WPCs), which are produced by blending wood and polymer materials, have attracted increasing attentions in market and industry due to the low cost and excellent performance. In this research, we have successfully engineered WPC by melt blending Polylactic Acid (PLA) and Poly(butylene adipate-co-terphthalate) (PBAT) with recycled wood flour. The thermal property and flammability of the composite are significantly improved by introducing flame retardant agent resorcinol bis(biphenyl phosphate) (RDP). The mechanical and morphological properties are also investigated via multiple techniques. The results show that wood material has increased toughness and impact resistance of the PLA/PBAT polymer matrix. SEM images have confirmed that PLA and PBAT are immiscible, but the incompatibility is reduced by the addition of wood. RDP is initially dispersed in the blends evenly. It migrates to the surface of the sample after flame application, and serves as a barrier between the fire and underlying polymers and wood mixture. It is well proved in the research that RDP is an efficient flame retardant agent in the WPC system.

  15. Fatigue damage mechanisms in short fiber reinforced PBT+PET GF30

    International Nuclear Information System (INIS)

    Research highlights: → Final macroscopic cracking only affects the few last percent of the lifetime → Classical approach based on fracture surface observation is not sufficient to characterize micro-mechanisms → Different techniques (scanning electron microscopy, replica technique, infra-red imaging) are compared to the macroscopic mechanical behavior evolution (stiffness, viscous damping, ratcheting effect) → The influence of surrounding fibers on some observed damage processes is being evidenced for the first time. - Abstract: The fatigue damage of a glass-reinforced PolyButylene Terephthalate and PolyEthylene Terephthalate with the fiber volume fraction of 30% (PBT+PET GF30) is investigated by means of various techniques. Fatigue tests at R = 0.1 are carried out on dogbone specimens and tubular specimens with different fiber orientations. The macroscopic evolution of the material behavior is evaluated and fatigue damage mechanisms are observed with a replica technique, Infrared imaging and scanning electron microscopy. A fatigue damage scenario is finally proposed. It is shown that the propagation of a single macroscopic crack is not the major fatigue mechanism under fatigue loading. Damage is spatially distributed in the material and the classical circular crack at the end of the fiber is confirmed as the based fatigue mechanisms. It is also shown that the damage observed alongside the fibers is related to spatial distribution of fiber rather than stress distribution around one single fiber.

  16. Morphology and Mechanical Properties of Nylon 6/PBT Blends Compatibilized with Styrene/Maleic Anhydride Copolymer

    Institute of Scientific and Technical Information of China (English)

    QIN Shu-hao; YU Jie; ZHENG Qiang; HE Min; ZHU Hong

    2007-01-01

    The mechanical properties and dynamic mechanical properties of blends composed of Nylon 6 and poly( butylenes terephthalate) (PBT), with styrene/maleic anhydride(SMA) as compatibilizer, were studied. The observation on the morphologies of the etched surfaces of the cryogenically fractured specimens via scanning electron microscopy(SEM)demonstrated that in the compatibilized Nylon 6/PBT blends, there exists a finer and more uniform dispersion induced by thein-situ interfacial chemical reactions during the preparation than that in the corresponding uncompatibilized blends. On the other hand, the overall mechanical properties of the compatibilized blends could be remarkably improved compared with those of the uncompatibilized ones. Moreover, increasing the amount of the compatibilizer SMA leads to a more efficient dispersion of the PBT phase in Nylon 6/PBT blends. Furthermore, there exists an optimum level of SMA added to achieve the maximum mechanical properties. As far as the mechanism of this reactive compatibilization is concerned, the enhanced interfacial adhesion is necessary to obtain improved dispersion, stable phase morphology, and better mechanical properties.

  17. Preparation and application of conducting polymer/Ag/clay composite nanoparticles formed by in situ UV-induced dispersion polymerization.

    Science.gov (United States)

    Zang, Limin; Qiu, Jianhui; Yang, Chao; Sakai, Eiichi

    2016-02-03

    In this work, composite nanoparticles containing polypyrrole, silver and attapulgite (PPy/Ag/ATP) were prepared via UV-induced dispersion polymerization of pyrrole using ATP clay as a templet and silver nitrate as photoinitiator. The effects of ATP concentration on morphology, structure and electrical conductivity were studied. The obtained composite nanoparticles with an interesting beads-on-a-string morphology can be obtained in a short time (10 min), which indicates the preparation method is facile and feasible. To explore the potential applications of the prepared PPy/Ag/ATP composite nanoparticles, they were served as multifunctional filler and blended with poly(butylene succinate) (PBS) matrix to prepare biodegradable composite material. The distribution of fillers in polymer matrix and the interfacial interaction between fillers and PBS were confirmed by scanning electron microscope, elemental mapping and dynamic mechanical analysis. The well dispersed fillers in PBS matrix impart outstanding antibacterial property to the biodegradable composite material as well as enhanced storage modulus due to Ag nanoparticles and ATP clay. The biodegradable composite material also possesses modest surface resistivity (10(6)~ 10(9) Ω/◻).

  18. Catalytic reactions of C4 hydrocarbons on the fluid catalytic cracking catalyst%C4烃类在催化裂化催化剂上催化转化反应的研究

    Institute of Scientific and Technical Information of China (English)

    闫平祥; 孟祥海; 徐春明; 高金森

    2008-01-01

    The catalytic reactions of C4 hydrocarbons on a fluid catalytic cracking (FCC) catalyst were studied in a confined fluidized bed reactor. The effect of reaction temperature and space velocity on product yields and distribution was investigated. The results show that the FCC catalyst has the good performance of aromatization and cracking of C4 hydrocarbons and can be used to produce propylene and aromatics under the suitable reaction conditions. It is mainly the butylene in the C4 hydrocarbons that undergoes catalytic reactions over the FCC catalyst and butane is hard to convert. Low reaction temperature favors the production of aromatics, while high reaction temperature favors the production of propylene. Low space velocity is beneficial to promote the conversion of butylene and the production of both aromatics and propylene. According to the bimolecular mechanism and reaction results, the reaction network for the catalytic reactions of C4 hydrocarbons on the FCC catalyst is proposed. The analysis on the this reaction mechanism indicates that the main reason of resulting in the lower yields of ethylene and propylene could be the poor secondary cracking performances of C5 and C6 olefins formed in the catalytic conversion of C4 hydrocarbons on the FCC catalyst.%利用小型固定流化床实验装置,对C4烃类在催化裂化催化剂上催化转化反应规律进行了实验研究,考察了不同反应温度及空速对C4烃类催化转化反应的产物分布和组成的影响.实验结果表明,催化裂化催化剂对C4烃类具有一定芳构化和裂化性能,在适宜的反应条件下,可增产芳烃和丙烯;在C4烃类催化转化过程中,丁烯是主要的反应物,而丁烷几乎不反应;低反应温度有利于增产芳烃,高反应温度有利于增产丙烯.较低的空速对增产芳烃和丙烯都有利.根据双分子反应机理和反应结果 ,建立了C4烃类在催化裂化催化剂上催化转化过程的反应网络.对C4烃类催化转化

  19. Caracterização de géis termorreversíveis de SEBS Characterization of thermoreversible gels of SEBS

    Directory of Open Access Journals (Sweden)

    Antonio José F. Carvalho

    2000-03-01

    Full Text Available RESUMO: Géis termorreversíveis preparados a partir de um copolímero em bloco de estireno - etileno/butileno - estireno (SEBS e polietileno de baixa densidade dissolvidos em óleos minerais parafínicos e óleos polibutênicos, bem como em suas misturas, foram preparados e caracterizados por calorimetria diferencial de varredura (DSC e análise dinâmico mecânica (DMA. Os termogramas obtidos por DMA mostraram um comportamento bastante distinto em função do óleo utilizado como solvente. O valor de Tg e o módulo de estocagem, G' correspondente à temperatura de "onset" variaram de 25 a 47ºC e 0,25 a 9 MPa, respectivamente. Os géis compostos com óleos parafínicos apresentaram os maiores valores de Tg e de G'. As análises de DSC revelaram um pico endotérmico que foi designado como sendo de dissolução, entre 75°C e 90°C e o correspondente pico exotérmico (60°C e 40°C verificado durante o resfriamento. Esse processo de dissolução foi atribuído aos processos de fusão e solvatação dos cristalitos de polietileno. As transições observadas por DMA estão relacionadas aos domínios de poliestireno do copolímero em bloco, em conjunto com as transições do polietileno e são muito afetadas pelo tipo de solvente. Os géis estudados apresentam dois mecanismos distintos de gelificação, via formação de cristalitos de polietileno e via formação de agregados de poliestireno dos blocos terminais do SEBS. O efeito dos óleos aromáticos e naftênicos sobre o módulo dos materiais foi relacionado com um aumento na interação entre os agregados de poliestireno e a fase etileno-butileno.Thermoreversible gels of styrene-ethylene/butylene-styrene block copolymers (SEBS and low density polyethylene dissolved in mineral paraffinic and polybutene oils, as well its mixtures, were prepared and characterized by differential scanning calorimetry (DSC and dynamic mechanical analysis (DMA. DMA analysis showed distinct behavior depending on the

  20. 可降解聚酯酰胺共聚物的合成及其性能研究%The synthesis and performance of biodegradable polyester amide copolymer

    Institute of Scientific and Technical Information of China (English)

    刘跃军; 冯正洋; 戴红; 石璞

    2015-01-01

    以丁二酸、丁二醇、1,6-己二胺为原料,二丁基二月桂酸锡为催化剂,甲苯二异氰酸酯(TDI)为扩链剂,通过熔融共聚,合成了 M w为40~65 k 的聚丁二酸-丁二醇-1,6-己二胺共聚物,并采用压延成膜法制得聚酯酰胺薄膜.研究了1,6-己二胺含量对聚酯酰胺的热性能、结晶性能、降解性能和流变性能的影响.结果表明,合成了聚酯酰胺,其熔点达到100.97℃,热分解温度为317.85℃;随着1,6-己二胺添加量增加,聚酯酰胺的拉伸强度不断变大,断裂伸长率略有下降;1,6-己二胺的加入并未改变聚酯酰胺的晶型,但降低了其结晶度;1,6-己二胺的加入提高了聚酯酰胺降解性能,而且改善了其流变性能,这有利于聚酯酰胺的成型加工和应用.%Succinic acid-butanediol-1,6-hexamethylenediamine polyester amide copolymers with Mw from 40 000 to 65 000 were synthesized by succinic acid,1,4-butylene and 1,6-hexamethylenediamine,through high temper-ature melt reaction.Meanwhile,the second dibutyl tin laurate was selected as catalyst,and the toluene disocya-nate (TDI)was selected as chain extender.The succinic acid-butylene-adipic amine copolymer films were pre-pared by calendering film-forming method.The influences of the content of 1,6-adipic amine on the copolymer performance of thermal,crystallization,degradation and rheological properties were researched.The results showed that the polyester amide copolymers were synthesized successfully,whose melting point is 100.97 ℃and the thermal decomposition temperature is 317.85 ℃.With the increasing of 1,6-adipic amine,the tensile strength of copolymers increased accordingly,and the elongation at break decreased slightly.1,6-adipic amine did not change the crystal type of copolymer,but the crystallinity of copolymer decreased.With adding the 1,6-adipic amine in copolymer,the degradation performance and rheological properties of the copolymers were im-proved,which is useful for the

  1. Temperature-dependent absorption cross-section measurements of 1-butene (1-C4H8) in VUV and IR

    KAUST Repository

    Es-sebbar, Et-touhami

    2013-01-01

    Vacuum ultraviolet (VUV) and infrared (IR) absorption cross-section measurements of 1-butene (1-C4H8; CH2=CHCH2CH3; Butylene) are reported over the temperature range of 296-529K. The VUV measurements are performed between 115 and 205nm using synchrotron radiation as a tunable VUV light source. Fourier Transform Infrared (FTIR) spectroscopy is employed to measure absorption cross-section and band strengths in the IR region between 1.54 and 25μm (~6500-400cm-1). The measured room-temperature VUV and IR absorption cross-sections are compared with available literature data and are found to be in good agreement. The oscillator strength for the electronic transition (A1A\\'→X1A\\') around 150-205nm is determined to be 0.32±0.01.The gas temperature has a strong effect on both VUV and IR spectra. Measurements made in the VUV region show that the peak value of the band cross-section decreases and the background continuum increases with increasing gas temperature. This behavior is due to a change in the rotational and vibrational population distribution of 1-butene molecule. Similar changes in rotational population are observed in the IR spectra. Moreover, variation of the IR spectra with temperature is used to measure the enthalpy difference between syn and skew conformations of 1-butene and is found to be 0.24±0.03. kcal/mol, which is in excellent agreement with values reported in the literature. The measurements reported in this work will provide the much-needed spectroscopic information for the development of high-temperature quantitative diagnostics in combustion applications and validation of atmospheric chemistry models of extra-solar planets. © 2012 Elsevier Ltd.

  2. Effect of the Modified Fiber on the Performance of PBS Composite%秸秆纤维的改性对PBS复合材料性能的影响

    Institute of Scientific and Technical Information of China (English)

    丁芳芳; 张敏; 李成涛; 葛正浩; 梁金生

    2011-01-01

    Composite made by modified corn stalk fiber/poly butylene succinate (PBS) were prepared by hot-pressing technology, and the effect of five different modifiers such as phenylformic acid, stearic acid, silane, chitosan and acetic acid on the fiber/PBS composite was studied. Energy disperse spectroscopy, scanning electron microscopy,infrared spectroscopy and Xray diffraction were used to characterize the modified fiber and the composite. The results showed that every modifier showed some effects on the modified fiber. Compared with the different modifiers and its addition on the properties of composite,found that when the acid content was 2 % ~ 3 % ,the performance of the composite was the best.%采用改性剂改性后的玉米秸秆纤维增强聚丁二酸丁二醇酯(PBS),利用热压工艺得到了秸秆纤维/PBS复合材料;研究了苯甲酸、硬脂酸、硅烷、壳聚糖及乙酸5种改性剂对经超声波处理后的秸秆纤维/PBS复合材料性能的影响;采用EDS、SEM、FTIR及WXRD对改性前后的纤维及复合材料进行了分析.研究结果表明:5种改性剂对纤维均有改性效果,苯甲酸质量分数为2%-3%时,复合材料力学性能最优.

  3. Extremely supercharged proteins in mass spectrometry: profiling the pH of electrospray generated droplets, narrowing charge state distributions, and increasing ion fragmentation.

    Science.gov (United States)

    Zenaidee, Muhammad A; Donald, William A

    2015-03-21

    The effects of 12 acids, 4 solvents, and 8 low-volatility additives that increase analyte charging (i.e., superchargers) on the charge state distributions (CSDs) of protein ions in ESI-MS were investigated. We discovered that (i) relatively low concentrations [5% (v/v)] of 1,2-butylene carbonate (and 4-vinyl-1,3-dioxolan-2-one) can be added to ESI solutions to form higher charge states of cytochrome c and myoglobin ions than by using more traditional additives (e.g., propylene carbonate, sulfolane, or m-nitrobenzyl alcohol) under these conditions and (ii) the width of CSDs narrow as the effectiveness of superchargers increase, which concentrates protein ions into fewer detection channels. The use of strong acids (pKa values 0) results in significantly higher protein ion charging, less acid adduction, and narrower CSDs, indicating that protein ion supercharging in ESI can be significantly limited by the binding of conjugate base anions of acids that neutralize charge sites and broaden CSDs. The extent of protein charging as a function of acid identity (HA) does not strongly correlate with gas-phase proton transfer data (i.e., gas-phase basicity and proton affinity values for HA and A(-)), solution-phase protein secondary structures (as determined by circular dichroism spectroscopy), and/or acid molecule volatility data. For protein-denaturing solutions, these data were used to infer that the "effective" pH of ESI generated droplets near the moment of ion formation can be ∼0, which is ca. 1 to 3 pH units lower than the pH of the solutions prior to ESI. Electron capture dissociation (ECD) of [ubiquitin, 17H](17+) resulted in the identification of 223 cleavages, 74 of 75 inter-residue sites, and 92% ECD fragmentation efficiency, which correspond to highest of these values that have been obtained by ECD of a single isolated charge state of ubiquitin.

  4. Principles of hierarchical meso- and macropore architectures by liquid crystalline and polymer colloid templating.

    Science.gov (United States)

    Sel, Ozlem; Kuang, Daibin; Thommes, Matthias; Smarsly, Bernd

    2006-02-28

    The generation of porous silica with hierarchically organized bimodal mesoporosity of adjustable size and well-defined shape was investigated by using surfactant mixtures and the nanocasting procedure (liquid crystalline templating). A systematic study of combinations of various block copolymers (Pluronics F127, KLE (poly(omega-hydroxypoly(ethylene-co-butylene)-co-poly(ethylene oxide))) and SE (PS-co-PEO)) with smaller surfactants (Pluronics P123, C16mimCl, and CTAB) revealed that hierarchical bimodal mesopore architectures could only be obtained by the usage of block copolymers with a strong hydrophilic-hydrophobic contrast, such as KLE and SE, giving rise to pores between 6 and 22 nm. Furthermore, the ionic liquid (IL) C16mimCl appeared to have advantageous templating properties, resulting in 2-3-nm pores being located between the block copolymer mesopores, whereas phase separation was observed for Pluronics and CTAB as small templates. Thereby, the study provided also general insights into the mixing and co-self-assembly behavior of block copolymers and ionic surfactants in water and confirmed the special templating properties of ILs, as recently proposed. In addition to the bimodal mesoporosity, additional tunable macroporosity was created by the presence of poly(styrene) or poly(methyl methacrylate) spheres, leading to well-defined trimodal hierarchical pore architectures with the small pores being located in the walls of the respective larger pores. As a major improvement, due to the pore hierarchy, these large-pore materials showed relatively large surface areas and pore volumes, and the size of densely packed macropores could even be decreased down to 90 nm. The materials were characterized by electron microscopy, small-angle X-ray scattering, and nitrogen sorption using a proper NLDFT (nonlocal density functional theory) approach for calculations of the pore size distribution in the entire range of micro- and mesopores. PMID:16489823

  5. Conductive porous scaffolds as potential neural interface materials.

    Energy Technology Data Exchange (ETDEWEB)

    Hedberg-Dirk, Elizabeth L.; Cicotte, Kirsten N.; Buerger, Stephen P.; Reece, Gregory; Dirk, Shawn M.; Lin, Patrick P.

    2011-11-01

    Our overall intent is to develop improved prosthetic devices with the use of nerve interfaces through which transected nerves may grow, such that small groups of nerve fibers come into close contact with electrode sites, each of which is connected to electronics external to the interface. These interfaces must be physically structured to allow nerve fibers to grow through them, either by being porous or by including specific channels for the axons. They must be mechanically compatible with nerves such that they promote growth and do not harm the nervous system, and biocompatible to promote nerve fiber growth and to allow close integration with biological tissue. They must exhibit selective and structured conductivity to allow the connection of electrode sites with external circuitry, and electrical properties must be tuned to enable the transmission of neural signals. Finally, the interfaces must be capable of being physically connected to external circuitry, e.g. through attached wires. We have utilized electrospinning as a tool to create conductive, porous networks of non-woven biocompatible fibers in order to meet the materials requirements for the neural interface. The biocompatible fibers were based on the known biocompatible material poly(dimethyl siloxane) (PDMS) as well as a newer biomaterial developed in our laboratories, poly(butylene fumarate) (PBF). Both of the polymers cannot be electrospun using conventional electrospinning techniques due to their low glass transition temperatures, so in situ crosslinking methodologies were developed to facilitate micro- and nano-fiber formation during electrospinning. The conductivity of the electrospun fiber mats was controlled by controlling the loading with multi-walled carbon nanotubes (MWNTs). Fabrication, electrical and materials characterization will be discussed along with initial in vivo experimental results.

  6. 聚(丁二酸丁二醇酯丁二酸环己烷二甲醇酯)的合成与表征%Synthesis and Characterization of Copolyesters of Succinic Acid-1,4-Butanediol/Succinic Acid-1,4-Cyclohexanedimethanol

    Institute of Scientific and Technical Information of China (English)

    余瑾; 程小苗; 周艺峰; 聂王焰

    2009-01-01

    用熔融缩聚法合成了一系列聚(丁二酸丁二醇酯丁二酸环己烷二甲醇酯)的无规共聚物.用FT-IR,~1H-NMR,DSC,TGA,XRD及水降解测试等方法表征了材料的结构与性能.通过DSC和TGA分析得到产物的熔点虽然较聚丁二酸丁二醇酯(PBS)有所降低,但是热分解温度却得到了提高;XRd测试结果表明,共聚物的晶体结构并没有发生改变;水降解测试结果表明,共聚物较PBS的降解速率有所提高.%A series of copolyesters of succinic acid-1,4-butanediol/succinic acid-1,4-cycl- ohexanedimethanol were synthesized and characterized by means of Fourier transform infrared spectroscopic(FT-IR), hydrogen nuclear magnetic resonance spectrum (~1H-NMR), differential scanning calorimetry ( DSC), thermogravimetry analysis (TGA), X-ray diffraction (XRD) and hydrolytic degradation. Though the melting temperature decreased, the copolymers showed the higher thermal decomposition temperature which was justified by TGA. X-ray diffraction shows that the crystal structure of copolymers is the same as poly (butylene succinate) (PBS). The results of hydrolytic degradation show that the rate of biodegradation of copolymers are higher than that of PBS.

  7. Interfacing polymeric scaffolds with primary pancreatic ductal adenocarcinoma cells to develop 3D cancer models.

    Science.gov (United States)

    Ricci, Claudio; Mota, Carlos; Moscato, Stefania; D'Alessandro, Delfo; Ugel, Stefano; Sartoris, Silvia; Bronte, Vincenzo; Boggi, Ugo; Campani, Daniela; Funel, Niccola; Moroni, Lorenzo; Danti, Serena

    2014-01-01

    We analyzed the interactions between human primary cells from pancreatic ductal adenocarcinoma (PDAC) and polymeric scaffolds to develop 3D cancer models useful for mimicking the biology of this tumor. Three scaffold types based on two biocompatible polymeric formulations, such as poly(vinyl alcohol)/gelatin (PVA/G) mixture and poly(ethylene oxide terephthalate)/poly(butylene terephthalate) (PEOT/PBT) copolymer, were obtained via different techniques, namely, emulsion and freeze-drying, compression molding followed by salt leaching, and electrospinning. In this way, primary PDAC cells interfaced with different pore topographies, such as sponge-like pores of different shape and size or nanofiber interspaces. The aim of this study was to investigate the influence played by the scaffold architecture over cancerous cell growth and function. In all scaffolds, primary PDAC cells showed good viability and synthesized tumor-specific metalloproteinases (MMPs) such as MMP-2, and MMP-9. However, only sponge-like pores, obtained via emulsion-based and salt leaching-based techniques allowed for an organized cellular aggregation very similar to the native PDAC morphological structure. Differently, these cell clusters were not observed on PEOT/PBT electrospun scaffolds. MMP-2 and MMP-9, as active enzymes, resulted to be increased in PVA/G and PEOT/PBT sponges, respectively. These findings suggested that spongy scaffolds supported the generation of pancreatic tumor models with enhanced aggressiveness. In conclusion, primary PDAC cells showed diverse behaviors while interacting with different scaffold types that can be potentially exploited to create stage-specific pancreatic cancer models likely to provide new knowledge on the modulation and drug susceptibility of MMPs.

  8. Control of enzymatic degradation of biodegradable polymers by treatment with biosurfactants, mannosylerythritol lipids, derived from Pseudozyma spp. yeast strains.

    Science.gov (United States)

    Fukuoka, Tokuma; Shinozaki, Yukiko; Tsuchiya, Wataru; Suzuki, Ken; Watanabe, Takashi; Yamazaki, Toshimasa; Kitamoto, Dai; Kitamoto, Hiroko

    2016-02-01

    Cutinase-like esterase from the yeasts Pseudozyma antarctica (PaE) shows strong degradation activity in an agricultural biodegradable plastic (BP) model of mulch films composed of poly(butylene succinate-co-adipate) (PBSA). P. antarctica is known to abundantly produce a glycolipid biosurfactant, mannosylerythritol lipid (MEL). Here, the effects of MEL on PaE-catalyzed degradation of BPs were investigated. Based on PBSA dispersion solution, the degradation of PBSA particles by PaE was inhibited in the presence of MEL. MEL behavior on BP substrates was monitored by surface plasmon resonance (SPR) using a sensor chip coated with polymer films. The positive SPR signal shift indicated that MEL readily adsorbed and spread onto the surface of a BP film. The amount of BP degradation by PaE was monitored based on the negative SPR signal shift and was decreased 1.7-fold by MEL pretreatment. Furthermore, the shape of PBSA mulch films in PaE-containing solution was maintained with MEL pretreatment, whereas untreated films were almost completely degraded and dissolved. These results suggest that MEL covering the surface of BP film inhibits adsorption of PaE and PaE-catalyzed degradation of BPs. We applied the above results to control the microbial degradation of BP mulch films. MEL pretreatment significantly inhibited BP mulch film degradation by both PaE solution and BP-degradable microorganism. Moreover, the degradation of these films was recovered after removal of the coated MEL by ethanol treatment. These results demonstrate that the biodegradation of BP films can be readily and reversibly controlled by a physical approach using MEL. PMID:26512003

  9. DSC and X-ray diffraction studies on the physicochemical changes occurring in polyester films exposed to heavy ion irradiation

    International Nuclear Information System (INIS)

    Poly(ethylene terephthalate) (PET) (commercial biaxially oriented Mylar and Hostaphan, 23 and 19 μm thick) and poly(butylene terephthalate) (PBT) (80μm thick) films were exposed to heavy ion irradiation and the resulting structural transformations were studied by differential scanning calorimetry (Perkin-Elmer DSC-7, heating rate in nitrogen flow , 2 or 3 K/min, open pans; heating cooling-heating cycles run at rates of 10-10-10 K/min, and 2-20-2 K/min, closed pans), wide-angle and small angle X-ray scattering (WAXS and SAXS), Fourier transform infrared spectroscopy (FTIR), gel permeation chromatography (GPC), and density measurements. The PBT film was prepared from the molten phase and then heated at 150oC. They were irradiated with Ar ions (5.5 MeV/amu, 1011 ions /cm2), Dy ions (13 MeV/amu, 1-5x1010 and 1011 ions/cm2), and Pb ions (11.4 MeV/amu, 1010 ions/cm2). The calculated radiation doses were found to be contained with the range of (1.1-22.0)x105 Gy. The irradiation-effected different film melting and crystallization courses detected by DSC and the changes in reflection intensities in WAXS diffractograms indicated to a reduced crystal phase content in the irradiated polyester films. The amorphization of the PET film was confirmed by SAXS and FTIR spectra and also by density measurements. As found by GPC, the molecular weight of the soluble fraction in PET decreases on irradiation and the accompanying increase in the content of the insoluble phase indicates that cross-linking process occur. The DSC and X-ray techniques proved to be helpful in following the structural changes induced in polymer films by irradiation with heavy ions. (author)

  10. DSC analysis of EB-cured polyurethane-acrylate

    International Nuclear Information System (INIS)

    The gel films obtained by electron beam (EB) solid-state polymerization of urethane-acrylate prepolymers were characterized by differential scanning calorimetry (DSC). Two kinds of urethane-acrylates were synthesized by reaction of poly(butylene adipate)diol (PBAD), 4,4'-diphenylmethane diisocyanate (MDI) and 2-hydroxyethyl acrylate (HEA) for this purpose. One is a semicrystalline prepolymer (UA-251M) with a number average molecular weight (M-barn) of 3200, and the other is an amorphous one (UA-071M) with M-barn of 1450. The M-barn varied by changing M-barn of PBAD. UA-251M gel film decreased in glass transition temperature (Tg) and increased in heat capacity change (ΔCp) at Tg with increasing irradiation dose, while the Tg and ΔCp values of UA-071M gel film changed in the opposite way to those of UA-251M gel film. Above 5 Mrad, gel fraction reached more than 90 %, and the Tg and ΔCp values changed steeply for both prepolymers. This steep change in Tg and ΔCp was attributed to the crosslinking of PBAD chains as well as of terminal acryloyl groups. Since the Tg change of UA-071M gel film depends merely on the crosslinking, the crosslinking structure was evaluated using two equations which relate the shift in Tg to crosslinking. The molecular weight between crosslinking junctions was found to be larger than the M-barn of the prepolymer. The crosslinking by the EB polymerization restricted the mobility of the polymer chain less strongly than the crosslinking by the three-functional isocyanate and α,ω-dihydroxy(polypropylene oxide) with a molecular weight of 1000 did. (author)

  11. DSC analysis of EB-cured polyurethane-acrylate

    Energy Technology Data Exchange (ETDEWEB)

    Ando, Masayuki; Uryu, Toshiyuki

    1987-10-01

    The gel films obtained by electron beam (EB) solid-state polymerization of urethane-acrylate prepolymers were characterized by differential scanning calorimetry (DSC). Two kinds of urethane-acrylates were synthesized by reaction of poly(butylene adipate)diol (PBAD), 4,4'-diphenylmethane diisocyanate (MDI) and 2-hydroxyethyl acrylate (HEA) for this purpose. One is a semicrystalline prepolymer (UA-251M) with a number average molecular weight (M-bar/sub n/) of 3200, and the other is an amorphous one (UA-071M) with M-bar/sub n/ of 1450. The M-bar/sub n/ varied by changing M-bar/sub n/ of PBAD. UA-251M gel film decreased in glass transition temperature (T/sub g/) and increased in heat capacity change (..delta..C/sub p/) at T/sub g/ with increasing irradiation dose, while the T/sub g/ and ..delta..C/sub p/ values of UA-071M gel film changed in the opposite way to those of UA-251M gel film. Above 5 Mrad, gel fraction reached more than 90 %, and the T/sub g/ and ..delta..C/sub p/ values changed steeply for both prepolymers. This steep change in T/sub g/ and ..delta..C/sub p/ was attributed to the crosslinking of PBAD chains as well as of terminal acryloyl groups. Since the T/sub g/ change of UA-071M gel film depends merely on the crosslinking, the crosslinking structure was evaluated using two equations which relate the shift in T/sub g/ to crosslinking. The molecular weight between crosslinking junctions was found to be larger than the M-bar/sub n/ of the prepolymer. The crosslinking by the EB polymerization restricted the mobility of the polymer chain less strongly than the crosslinking by the three-functional isocyanate and ..cap alpha..,..omega..-dihydroxy(polypropylene oxide) with a molecular weight of 1000 did.

  12. 静电纺丝法制备PBS纳米纤维膜及缓释血小板内生长因子的PBS纳米纤维膜的生物活性评价%Preparation and Bioactivities of Electrospun PBS Nanofiber Membrane and Hybrid PBS Nanofiber Membrane of Sustained Release Growth Factors in Platelet

    Institute of Scientific and Technical Information of China (English)

    孙淑芬; 李男男; 刘敏; 刘译聪; 张英超; 周延民

    2012-01-01

    利用静电纺丝法制备了聚丁二酸丁二醇酯(PBS)纳米纤维膜及PBS和富血小板血浆(PRP)的混合纳米纤维膜.通过扫描电子显微镜、3-(4,5-甲基噻唑-2)-2,5-二苯基四氮唑溴盐(MTT)比色法、支架表面细胞荧光染色法、材料溶血行为及Elisa法检测体外释放综合评价了支架材料的性能及生物活性.结果表明,纳米纤维膜对人骨肉瘤细胞系MG63细胞增殖具有促进作用;生长因子在最初的突释后,随材料降解而缓释;支架材料溶血率为0.1475%(<5%),符合医用材料的溶血实验要求.%Poly(butylene succinate) (PBS) nanofiber membrane and hybrid nanofiber membrane of PBS and platelet-rich plasma(PRP) were prepared by electrospinning. The properties and bioactivities of scaffold materials were evaluated by means of scanning electron microscope ( SEM) , methyl thiazolyl tetrazolium ( MIT) , fluorescent staining and laser scanning co-focal microscope, hemolytic properties of materials and enzyme-linked immunosorbent assay(ELISA). The experiment results show that nanofiber membranes can accelerate the proliferation of human osteosarcoma MG63 cells line. Also, in vitro the growth factors in the scaffold material display a sustained release with the scaffold degrading after the initial burst release. In addition, hemolytic rate of scaffold material is 0. 1475% ( <5% ) , which meets the demand of hemolytic rate of medial materials.

  13. PBS对PLA/凹凸棒石黏土复合材料性能的影响%The Influence of PBS on the Properties of PLA/Attapulgite Clay Composite

    Institute of Scientific and Technical Information of China (English)

    卢玉献; 徐惠; 程晓春; 金叶玲; 吴洁

    2012-01-01

    在140℃,氮气保护的条件下,使L-丙交酯开环与凹凸棒石黏土(AT)表面上的(Si-OH)发生反应,生成的低分子量聚乳酸接枝到经过处理的凹凸棒石黏土上,然后将接枝凹凸棒石黏土与聚乳酸(PLA)聚丁二酸丁二醇酯(PBS)进行熔融共混,制备PLA/PBS/凹凸棒石黏土(AT)复合材料.通过FTIR、SEM、力学性能测试及维卡软化测试仪对复合材料进行分析和表征.实验结果表明,凹凸棒石黏土的最佳加入量为1.5%;PBS的加入可以大大提高PLA的韧性,当加入量为25%时,综合力学性能最佳.%The L-lactide was reacted with Si-OH on attapulgite clay surface via a ring-opening under the protection of nitrogen at 140 ℃ to produce polylactic acid oligomers, which were grafted onto the treated attapulgite clay(AT),and then they melted blending with polylactic acid (PLA) and poly (butylene succi-nate) (PBS) to obtain PLA/PBS/attapulgite clay (AT) composites. They were analysed and characterized by means of FTIR ,SEM .mechanical property testing and Vicat softening tester . The results showed that the best content of attapulgite was 1. 5%. The addition of PBS could greatly improve the toughness of PLA;for best mechanical properties,the optimal amount was 25%.

  14. 傅立叶变换红外吸收光谱法测定改性聚丙烯材料中苯乙烯-乙烯-丁烯-苯乙烯含量%Determination of SEBS in modified polypropylene materials by fourier transform infrared absorption spectrometry

    Institute of Scientific and Technical Information of China (English)

    蔡荣; 徐俊

    2012-01-01

    Objective: To establish a method for determination of the content of styrene - ethylene - butylene - sty-rene(SEBS) in modified polypropylene materials. Methods:The materials were hot - pressed into membranes and infrared absorption spectra were acquired. According to the Lambert - Beer law, the ratio of the specific peak height of styrene to that of polypropylene was calculated to determine SEBS content. Results: The linear range of SEBS content was from 2% to 20% with a correlation coefficient of 0. 9997. The LOD and the LOQ of SEBS were 0. 3% and 1. 0% respectively. The average recovery of the method was 103. 1%. Conclusions:The FT -infrared absorption spectrometric method is suitable for the determination of SEBS content in modified polypropylene materials.%目的:建立改性聚丙烯材料中苯乙烯-乙烯-丁烯-苯乙烯(SEBS)含量的测定方法.方法:将实验材料热压成膜,记录红外吸收光谱图,根据朗伯-比尔定律,用苯乙烯与聚丙烯对应特征吸收校正峰高的相对比值直接测定改性聚丙烯材料中SEBS含量.结果:SEBS含量在2% ~20%范围内与吸收峰高的线性关系良好,r=0.9996;SEBS的LOD和LOQ分别为0.3%和1.0%;平均回收率为103.1%.结论:傅立叶变换红外吸收光谱法可用于改性聚丙烯材料中SEBS含量的测定.

  15. Bare and Polymer-Coated Indium Tin Oxide as Working Electrodes for Manganese Cathodic Stripping Voltammetry.

    Science.gov (United States)

    Rusinek, Cory A; Bange, Adam; Warren, Mercedes; Kang, Wenjing; Nahan, Keaton; Papautsky, Ian; Heineman, William R

    2016-04-19

    Though an essential metal in the body, manganese (Mn) has a number of health implications when found in excess that are magnified by chronic exposure. These health complications include neurotoxicity, memory loss, infertility in males, and development of a neurologic psychiatric disorder, manganism. Thus, trace detection in environmental samples is increasingly important. Few electrode materials are able to reach the negative reductive potential of Mn required for anodic stripping voltammetry (ASV), so cathodic stripping voltammetry (CSV) has been shown to be a viable alternative. We demonstrate Mn CSV using an indium tin oxide (ITO) working electrode both bare and coated with a sulfonated charge selective polymer film, polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene-sulfonate (SSEBS). ITO itself proved to be an excellent electrode material for Mn CSV, achieving a calculated detection limit of 5 nM (0.3 ppb) with a deposition time of 3 min. Coating the ITO with the SSEBS polymer was found to increase the sensitivity and lower the detection limit to 1 nM (0.06 ppb). This polymer modified electrode offers excellent selectivity for Mn as no interferences were observed from other metal ions tested (Zn(2+), Cd(2+), Pb(2+), In(3+), Sb(3+), Al(3+), Ba(2+), Co(2+), Cu(2+), Ni(3+), Bi(3+), and Sn(2+)) except Fe(2+), which was found to interfere with the analytical signal for Mn(2+) at a ratio 20:1 (Fe(2+)/Mn(2+)). The applicability of this procedure to the analysis of tap, river, and pond water samples was demonstrated. This simple, sensitive analytical method using ITO and SSEBS-ITO could be applied to a number of electroactive transition metals detectable by CSV. PMID:26980322

  16. NOTE: Spectra from 2.5-15 µm of tissue phantom materials, optical clearing agents and ex vivo human skin: implications for depth profiling of human skin

    Science.gov (United States)

    Viator, John A.; Choi, Bernard; Peavy, George M.; Kimel, Sol; Nelson, J. Stuart

    2003-01-01

    Infrared measurements have been used to profile or image biological tissue, including human skin. Usually, analysis of such measurements has assumed that infrared absorption is due to water and collagen. Such an assumption may be reasonable for soft tissue, but introduction of exogenous agents into skin or the measurement of tissue phantoms has raised the question of their infrared absorption spectrum. We used Fourier transform infrared spectroscopy in attenuated total reflection mode to measure the infrared absorption spectra, in the range of 2-15 µm, of water, polyacrylamide, Intralipid, collagen gels, four hyperosmotic clearing agents (glycerol, 1,3-butylene glycol, trimethylolpropane, TopicareTM), and ex vivo human stratum corneum and dermis. The absorption spectra of the phantom materials were similar to that of water, although additional structure was noted in the range of 6-10 µm. The absorption spectra of the clearing agents were more complex, with molecular absorption bands dominating between 6 and 12 µm. Dermis was similar to water, with collagen structure evident in the 6-10 µm range. Stratum corneum had a significantly lower absorption than dermis due to a lower content of water. These results suggest that the assumption of water-dominated absorption in the 2.5-6 µm range is valid. At longer wavelengths, clearing agent absorption spectra differ significantly from the water spectrum. This spectral information can be used in pulsed photothermal radiometry or utilized in the interpretation of reconstructions in which a constant μir is used. In such cases, overestimating μir will underestimate chromophore depth and vice versa, although the effect is dependent on actual chromophore depth.

  17. Glyceryl monooleyl ether-based liquid crystalline nanoparticles as a transdermal delivery system of flurbiprofen: characterization and in vitro transport.

    Science.gov (United States)

    Uchino, Tomonobu; Murata, Akiko; Miyazaki, Yasunori; Oka, Toshihiko; Kagawa, Yoshiyuki

    2015-01-01

    Liquid crystalline nanoparticles (LCNs) were prepared using glyceryl monooleyl ether (GME) by the modified film rehydration method. Hydrogenated lecithin (HL), 1,3-butylene glycol (1,3-BG), and Poloxamer 407 were used as additives. The prepared LCN formulations were evaluated based on particle size, small-angle X-ray diffraction (SAXS) analysis, (1)H- and (19)F-NMR spectra, and in vitro skin permeation across Yucatan micropig skin. The composition (weight percent) of the LCN formulations were GME-HL-1,3-BG (4 : 1 : 15), 4% GME-based LCN and GME-HL-1,3-BG (8 : 1 : 15), 8% GME-based LCN and their mean particle sizes were 130-175 nm. Flurbiprofen 5 and 10 mg was loaded into 4% GME-based LCN and 8% GME-based LCN systems, respectively. The results of SAXS and NMR suggested that both flurbiprofen-loaded formulations consist of particles with reverse type hexagonal phase (formation of hexosome) and flurbiprofen molecules were localized in the lipid domain through interaction of flurbiprofen with the lipid components. Flurbiprofen transport from the LCN systems across the Yucatan micropig skin was increased compared to flurbiprofen in citric buffer (pH=3.0). The 8% GME-based LCN systems was superior to the 4% GME-based LCN for flurbiprofen transport. Since the internal hexagonal phase in the 8% GME-based LCN systems had a higher degree of order compared to the 4% GME-based LCN in SAXS patterns, the 8% GME-based LCN system had a larger surface area, which might influence flurbiprofen permeation. These results indicated that the GME-based LCN system is effective in improving the skin permeation of flurbiprofen across the skin.

  18. Heat Treatment of Polylactide-based Ternary Blends%聚乳酸基三元共混物的热处理

    Institute of Scientific and Technical Information of China (English)

    宋庆林; 桂宗彦; 程树军; 陆冲

    2012-01-01

    Three different kinds of heat treatment methods were applied to the blends of poly(lactic acid) (PLA)/poly(butylene adipate-co-terephthalate)(PBAT)/poly(propylene carbonate) (PPC). The blends were characterized with wide angle X-ray diffraction, differential scanning calorimetry, polarized optical microscopy, and scanning electron microscope, and the effects of the heat treatment process on the structures and properties of the blends were studied. The results show that: the crystallization of PLA in the blends promotes and the water vapour barrier property enhances after been annealed. The vapour barrier property of blends treated with first quenched and then annealed is better than that of blends treated with direct annealing.%采用3种热处理过程对聚乳酸(PLA)、聚(己二酸-对苯二甲酸丁二酯)(PBAT)和聚丙撑碳酸酯(PPC)的共混物进行了热处理.采用广角X射线衍射仪、差示扫描食热仪、偏光显微镜和扫描电子显微镜等对共混物进行了表征,研究了热处理过程对共混物结构和性能的影响.结果表明:退火处理促进了共混物中PLA的结晶,提高了共混物的水蒸气阻隔性;先淬火再退火相对于直接退火处理,共混物的水蒸气阻隔性较好.

  19. Cyclization Phenomena in the Sol-Gel Polymerization of a,w-Bis(triethoxysilyl)alkanes and Incorporation of the Cyclic Structures into Network Silsesquioxane Polymers

    Energy Technology Data Exchange (ETDEWEB)

    Alam, T.M.; Carpenter, J.P.; Dorhout, P.K.; Greaves, J.; Loy, D.A.; Shaltout, R.; Shea, K.J.; Small, J.H.

    1999-01-04

    Intramolecular cyclizations during acid-catalyzed, sol-gel polymerizations of ct,co- bis(tietioxysilyl)aWmes substintidly lengtien gelties formonomers witietiylene- (l), propylene- (2), and butylene-(3)-bridging groups. These cyclizations reactions were found, using mass spectrometry and %i NMR spectroscopy, to lead preferentially to monomeric and dimeric products based on six and seven membered disilsesquioxane rings. 1,2- Bis(triethoxysilyl)ethane (1) reacts under acidic conditions to give a bicyclic drier (5) that is composed of two annelated seven membered rings. Under the same conditions, 1,3- bis(triethoxysilyl)propane (2), 1,4-bis(triethoxysilyl)butane (3), and z-1,4- bis(triethoxysilyl)but-2-ene (10) undergo an intramolecular condensation reaction to give the six membemd and seven membered cyclic disilsesquioxanes 6, 7, and 11. Subsequently, these cyclic monomers slowly react to form the tricyclic dirners 8,9 and 12. With NaOH as polymerization catalyst these cyclic silsesquioxanes readily ~aeted to afford gels that were shown by CP MAS z%i NMR and infr=d spectroscopes to retain some cyclic structures. Comparison of the porosity and microstructwe of xerogels prepared from the cyclic monomers 6 and 7 with gels prepared directly from their acyclic precursors 2 and 3, indicate that the final pore structure of the xerogels is markedly dependent on the nature of the precursor. In addition, despite the fact that the monomeric cyclic disilsesquioxane species can not be isolated from 1-3 under basic conditions due to their rapid rate of gelation, spectroscopic techniques also detected the presence of the cyclic structures in the resulting polymeric gels.

  20. 基于流程模拟器和列队竞争算法的蒸馏优化设计%Optimization design of distillation process based on process simulator and line-up competition algorithm

    Institute of Scientific and Technical Information of China (English)

    李振华; 林子雄; 罗艳玲; 张宇; 鄢烈祥; 史彬

    2013-01-01

    An optimal method for distillation process design was proposed based on the process simulator and the line up competition algorithm (LCA).Taking the minimal total cost as the objective function,a non-convex mixed-integer nonlinear programming model for the optimization design of distillation process was set up,in which the distillation sequence and heat integration were considered.The simulation of distillation process and the optimal search by LCA were alternately implemented until the optimal solution was acquired.The method proposed was applied to the optimal design of separating 1-butylene from C4 mixture.The optimal distillation sequence and heat integration process structure as well as the optimal design and the operating parameters of each column were obtained.%文章提出了基于流程模拟器与列队竞争算法的蒸馏过程优化设计方法.以总费用最少为目标函数,建立了蒸馏过程优化设计的混合整数非线性规划模型,其中考虑了蒸馏序列和热集成情况.流程模拟器对蒸馏过程的模拟与列队竞争算法的优化搜索交替进行,迭代计算直到收敛到最优解.将文中提出的方法应用于从C4混合物中分离1-丁烯的蒸馏过程优化设计,得到了最优的蒸馏序列和热集成流程结构,以及各塔的最优设计与操作参数.

  1. Additive manufactured polymeric 3D scaffolds with tailored surface topography influence mesenchymal stromal cells activity.

    Science.gov (United States)

    Neves, Sara C; Mota, Carlos; Longoni, Alessia; Barrias, Cristina C; Granja, Pedro L; Moroni, Lorenzo

    2016-06-01

    Additive manufactured three-dimensional (3D) scaffolds with tailored surface topography constitute a clear advantage in tissue regeneration strategies to steer cell behavior. 3D fibrous scaffolds of poly(ethylene oxide terephthalate)/poly(butylene terephthalate) block copolymer presenting different fiber surface features were successfully fabricated by additive manufacturing combined with wet-spinning, in a single step, without any post-processing. The optimization of the processing parameters, mainly driven by different solvent/non-solvent combinations, led to four distinct scaffold types, with average surface roughness values ranging from 0.071 ± 0.012 μm to 1.950 ± 0.553 μm, average pore sizes in the x- and y-axis between 351.1 ± 33.6 μm and 396.1 ± 32.3 μm, in the z-axis between 36.5 ± 5.3 μm and 70.7 ± 8.8 μm, average fiber diameters between 69.4 ± 6.1 μm and 99.0 ± 9.4 μm, and porosity values ranging from 60.2 ± 0.8% to 71.7 ± 2.6%. Human mesenchymal stromal cells (hMSCs) cultured on these scaffolds adhered, proliferated, and produced endogenous extracellular matrix. The effect of surface roughness and topography on hMSCs differentiation was more evident for cells seeded at lower density, where the percentage of cells in direct contact with the surface was higher compared to more densely seeded scaffolds. Under osteogenic conditions, lower surface roughness values (0.227 ± 0.035 μm) had a synergistic effect on hMSCs behavior, while chondrogenesis was favored on rougher surfaces (1.950 ± 0.553 μm). PMID:27219645

  2. Spectra from 2.5-15 μm of tissue phantom materials, optical clearing agents and ex vivo human skin: implications for depth profiling of human skin

    International Nuclear Information System (INIS)

    Infrared measurements have been used to profile or image biological tissue, including human skin. Usually, analysis of such measurements has assumed that infrared absorption is due to water and collagen. Such an assumption may be reasonable for soft tissue, but introduction of exogenous agents into skin or the measurement of tissue phantoms has raised the question of their infrared absorption spectrum. We used Fourier transform infrared spectroscopy in attenuated total reflection mode to measure the infrared absorption spectra, in the range of 2-15 μm, of water, polyacrylamide, Intralipid, collagen gels, four hyperosmotic clearing agents (glycerol, 1,3-butylene glycol, trimethylolpropane, TopicareTM), and ex vivo human stratum corneum and dermis. The absorption spectra of the phantom materials were similar to that of water, although additional structure was noted in the range of 6-10 μm. The absorption spectra of the clearing agents were more complex, with molecular absorption bands dominating between 6 and 12 μm. Dermis was similar to water, with collagen structure evident in the 6-10 μm range. Stratum corneum had a significantly lower absorption than dermis due to a lower content of water. These results suggest that the assumption of water-dominated absorption in the 2.5-6 μm range is valid. At longer wavelengths, clearing agent absorption spectra differ significantly from the water spectrum. This spectral information can be used in pulsed photothermal radiometry or utilized in the interpretation of reconstructions in which a constant μir is used. In such cases, overestimating μir will underestimate chromophore depth and vice versa, although the effect is dependent on actual chromophore depth. (note)

  3. Identification of dominant lactic acid bacteria isolated from grape juices. Assessment of its biochemical activities relevant to flavor development in wine

    Directory of Open Access Journals (Sweden)

    Fabiana Maria Saguir

    2009-06-01

    Full Text Available Fabiana Maria Saguir1,3, Iris Eleonora Loto Campos1, Carmen Maturano1, Maria Cristina Manca de Nadra1,2,31Facultad de Bioquímica, Química y Farmacia, Universidad Nacional de Tucumán, Tucumán, Argentina; 2Centro de Referencia para Lactobacilos (Cerela, Tucumán, Argentina; 3Career Investigators from Consejo Nacional de Investigaciones Científicas y Técnicas, ArgentinaAbstract: We investigated the dominant lactic acid bacteria (LAB from grape juice and commencement of malolactic fermentation (MLF samples of a cellar located in Argentina and assessment of its β-glucosidase activity and butter aroma compounds production. LAB number found in grape juice (approximately log10 3.3 was lower than that obtained in the MLF samples. Oenococcus oeni was predominant, accounting for 68% of the 81 LAB isolated. Majority of whole cells derived from O. oeni cultures at the end of the exponential growth showed detectable β-glucosidase activity. Contrarily, the highest proportion of them did not produce diacetyl, acetoin, and 2,3-butylene glycol. A direct relation between both properties among the O. oeni strains could not be established. In the selected MS25 strain, L-malic acid was compatible with good enzyme activity and was partially able to annul the negative influence of the low pH (3.8. In different conditions, the aroma compounds were lower than 4 mg/ml, especially at pH 3.8 and in presence of L-malic acid (2.5 g/l. This strain could have adequate characteristics for potential use in winemaking. Finally, the assessment of both biochemical properties in O. oeni should be considered as a quality criterion for selecting starter cultures for the improvement of the wines aroma.Keywords: isolation, lactic acid bacteria, biochemical properties, aroma, wine

  4. Improving the Surface Wettability of PET Fiber by Epitaxial Crystallization%聚酯纤维的附生结晶法改善纤维的表面浸润性

    Institute of Scientific and Technical Information of China (English)

    王海军; 赵庭山; 石宝; 任龙芳; 强涛涛; 王学川

    2012-01-01

    将聚对苯二甲酸乙二醇酯(PET)纤维置入过冷态的聚乙二醇(PEG)和聚己二酸丁二酯(PBA)熔体,制备了PET纤维/PEG基体和PET纤维/PBA基体复合体系。使用偏光显微镜和原子力显微镜研究了这两种异质复合体系的界面结晶形态,利用接触角测量仪测量了附生结晶法改性前后PET纤维织物的接触角。结果表明,纤维置入温度和结晶等条件决定附生体系的横穿晶体形态结构,选取合适的树脂并采用附生结晶的方法可明显改善PET纤维织物的表面浸润性,并有望改善PET纤维增强复合材料内部的界面结构。%By introducing poly(ethylene terephthalate)(PET) fibers into supercooled molten poly(ethylene glycol)(PEG) and poly(butylene adipate)(PBA) matrices,fiber/matrix composites of PET/PBA and PET/PEG have been prepared.Their interfacial supermolecular structure was studied by polarizing microscope(POM) and atomic force microscope(AFM).The contact angle of water on PET fiber fabric was analyzed before and after epitaxial crystallization.The results show that the fiber introduction temperature and crystallization temperature control the interfacial transcrystallinity structure between PET fiber and the matrix.Epitaxial crystallization and employment of suitable resin matrix can significantly improve the surface wettability of PET fiber,which can probably improve the interfacial compatibility in PET fiber reinforced composite.

  5. Influence of processing sequence on the tribological properties of VGCF-X/PA6/SEBS composites

    Science.gov (United States)

    Osada, Yu; Nishitani, Yosuke; Kitano, Takeshi

    2016-03-01

    In order to develop the new tribomaterials for mechanical sliding parts with sufficient balance of mechanical and tribological properties, we investigated the influence of processing sequence on the tribological properties of the ternary nanocomposites: the polymer blends of polyamide 6 (PA6) and styrene-ethylene/butylene-styrene copolymer (SEBS) filled with vapor grown carbon fiber (VGCF-X), which is one of carbon nanofiber (CNF) and has 15nm diameter and 3μm length. Five different processing sequences: (1) VGCF-X, PA6 and SEBS were mixed simultaneously (Process A), (2) Re-mixing (Second compounding) of the materials prepared by Process A (Process AR),(3) SEBS was blended with PA6 (PA6/SEBS blends) and then these blends were mixed with VGCF-X (Process B), (4) VGCF-X was mixed with PA6 (VGCF-X/PA6 composites) and then these composites were blended with SEBS (Process C), and (5) VGCF-X were mixed with SEBS (VGCF-X/SEBS composites) and then these composites were blended with PA6 (Process D) were attempted for preparing of the ternary nanocomposites (VGCF-X/PA6/SEBS composites). These ternary polymer nanocomposites were extruded by a twin screw extruder and injection-molded. Their tribological properties were evaluated by using a ring-on-plate type sliding wear tester under dry condition. The tribological properties such as the frictional coefficient and the specific wear rate were influenced by the processing sequence. These results may be attributed to the change of internal structure formation, which is a dispersibility of SEBS particle and VGCF-X in ternary nanocomposites (VGCF-X/PA6/SEBS) by different processing sequences. In particular, the processing sequences of AR, B and D, which are those of re-mixing of VGCF-X, have a good dispersibility of VGCF-X for the improvement of tribological properties.

  6. Conductivity of microfibrillar polymer-polymer composites with CNT-loaded microfibrils or compatibilizer: A comparative study

    Directory of Open Access Journals (Sweden)

    S. Fakirov

    2013-07-01

    Full Text Available Conductive polymer composites have wide ranging applications, but when they are produced by conventional melt blending, high conductive filler loadings are normally required, hindering their processability and reducing mechanical properties. In this study, two types of polymer-polymer composites were studied: i microfibrillar composites (MFC of polypropylene (PP and 5 wt% carbon nanotube (CNT loaded poly(butylene terephthalate (PBT as reinforcement, and ii maleic anhydride-grafted polypropylene (PP-g-MA compatibilizer, loaded with 5 wt% CNTs introduced into an MFC of PP and poly(ethylene terephthalate (PET in concentrations of 5 and 10 wt%. For the compatibilized composite type, PP and PET were melt-blended, cold-drawn and pelletized, followed by dry-mixing with PP-g-MA/CNT, re-extrusion at 200°C, and cold-drawing. The drawn blends produced were compression moulded to produce sheets with MFC structure. Using scanning electron microscopy, CNTs coated with PP-g-MA could be observed at the interface between PP matrix and PET microfibrils in the compatibilized blends. The volume resistivities tested by four-point test method were: 2.87•108 and 9.93•107 Ω•cm for the 66.5/28.5/5 and 63/27/10 (by wt% PP/PET/(PP-g-MA/CNT blends, corresponding to total CNT loadings (in the composites of 0.07 vol% (0.24 wt% and 0.14 vol% (0.46 wt%, respectively. For the non-compatibilized MFC types based on PP/(PBT/CNT with higher and lower melt flow grades of PP, the resistivities of 70/(95/5 blends were 1.9•106 and 1.5•107 Ω•cm, respectively, corresponding to a total filler loading (in the composite of 0.44 vol% (1.5 wt% in both MFCs.

  7. Analysis of Flavoring Compositions in Persimmon Fruit Wine by GC/MS%柿子果酒香气成分的GC/MS分析

    Institute of Scientific and Technical Information of China (English)

    凌育赵; 刘经亮

    2011-01-01

    The flavoring compositions in persimmon fruit wine was extracted by solid phase microextraction (SPME), separated and analyzed by GC-MS. 62 Peaks were separated and 56 components were identified, accounting for 86.66% of the total area of chromatogram eluting peaks. Alcohols, esters and acids were the main flavoring compositions, including isoamyl alcohol (38.55%), Phenylethanol (14.50%), isoamyl formate (7.44%), 2-methy1-1- butanol (4.72%), 2-methoxybutyl acetate (2.25%), isobatyalcohol (1.98%), acetic acid (1.39%), tryptophol (1.22%), 1,3-butylene glycol (1.20%) and 2-hydroxy butyric acid (1.02%).%采用固相微萃取法提取、富集柿子果酒中的香气成分,经GC-MS分析,分离出62个峰,鉴定出56种化合物,占总峰面积86.66%,包括醇类、酯类、酸类等化合物.其中主要成分为异戊醇(38.55%)、苯乙醇(14.50%)、甲酸异戊酯(7.44%)、2-甲基-1-丁醇(4.72%)、乙酸-3-甲基丁酯(2.25%)、异丁醇(1.98%)、乙酸乙酯(1.39%)、吲哚-3-乙醇(1.22%)、1,3-丁二醇(1.20%)、4-羟基丁酸(1.02%).

  8. Six-month clinical outcomes of Firebird 2TM sirolimus-eluting stent implantation in real-world patients with coronary artery diseases

    Institute of Scientific and Technical Information of China (English)

    GE Jun-bo; ZHANG Feng; QIAN Ju-ying; GE Lei; LIU Xue-bo; ZHOU Jun

    2011-01-01

    Background The Firebird 2TM sirolimus-eluting stent (Firebird 2 stent) is a second-generation sirolimus-eluting stent which has a cobalt-chromium alloy stent platform, a brand new bracket structure, and two layers of styrene-butylenes-styrene polymer coatings with better biocompatibility. The Firebird 2TM cObalt-Chromium alloy sirolimus-elUting Stent registry (FOCUS registry) aimed to evaluate the safety and efficacy of the Firebird 2 stent in patients with coronary artery disease in daily practice.Methods The FOCUS registry is a prospective, non-randomized, international multi-center, single-arm clinical registry.Between March 2009 and February 2010, 5084 patients receiving at least 1 Firebird 2 stent during daily clinical practice at 83 medical centers were enrolled.Results Of the 5084 patients enrolled in the registry, 5077 and 5058 were respectively available for 30 days and 6 months follow-up. The 30-day rate of major adverse cardiac events (MACE) was 1.20%, including 13 cardiac deaths, 46 non-fatal myocardial infarction (MI), and 6 target vessel revascularization (TVR). At 6 months follow-up, the rate of MACE was 1.80%. There were 32 cardiac deaths, 48 non-fatal MI, and 15 TVR. According to the Academic Research Consortium definition, definite/probable stent thrombosis (ST) occurred in 0.43% (22/5058) of patients, including 8 cases of acute ST, 11 subacute ST, and 3 late ST.Conclusion The Firebird 2 stent showed the promising efficacy and safety at 30 days and 6 months in a real-world population of patients with coronary artery diseases.

  9. STUDY ON THE CRYSTALLIZATION BEHAVIOR OF PLA/PBS/DCP REACTIVE BLENDS%PLA/PBS/DCP反应共混体系的结晶行为研究

    Institute of Scientific and Technical Information of China (English)

    季得运; 刘正英; 兰小蓉; 吴枫; 华笋; 杨鸣波

    2012-01-01

    The poly ( lactic acid ) /poly ( butylene succinate ) ( PLA/PBS ) blends with and without dicumyl peroxide ( DCP) were prepared by melt mixing and the crystallization behaviors of the blends were investigated using a differential scanning calorimeter ( DSC ) . The results showed that the crystallization ability of PLA was not improved when it was blended with PBS because of the higher molecular weight of PBS than that of PLA in this research,which was not in accord with results of some other researchers. However,the crystallization ability of PLA in the reactive blends (PLA/PBS/DCP) was promoted after the addition of different amount of DCP, because some crosslinked ( or grafted) structures were generated in this matrix, and the crosslinked ( or grafted) structures acted as nucleating points. It is found that when the content of DCP was from 0. 1 phr to 0. 3 phr, the crystallization was mostly caused by PBS, and this crystallization reduced with increasing the DCP content. When the content of DCP was above 0. 3 phr,that is to say,PLA began to crystallize when the DCP content was 0. 4 phr. The crystallization of PLA was enhanced with further increasing the content of DCP,while the crystallization of PBS was weakened in the same situation. In other words, the crystallization behavior of PLA and PBS in the PLA/PBS/DCP reactive blends was mostly depended on the DCP content.%通过熔融共混法制备了一系列聚乳酸(PLA)/聚丁二酸丁二醇酯(PBS)物理共混试样及PLA/PBS/过氧化二异丙苯(DCP)反应共混试样,采用示差扫描量热分析(DSC)法研究了物理共混试样结晶行为及反应共混试样的特殊结晶行为.结果发现,PLA与PBS的物理共混并未改善PLA的结晶性,而PLA/PBS/DCP反应共混时生成的交联/支化结构可起到异相成核作用,从而明显改善了反应共混体系的结晶性能,且随着DCP含量的增加,共混体系中两相结晶行为出现交替变化.

  10. High density polyethylene (HDPE)/poly(ethylene terephthalate) (PET) polymer blend studies related to recycling co-mingled plastics

    Science.gov (United States)

    Tsai, Pang-Yen

    Polymer blends of virgin high density polyethylene (HDPE) and poly(ethylene terephthalate) (PET) were studied as an attempt to relate the microstructure to the mechanical properties of the blends. The virgin blends were prepared by extrusion and then injection molded into specimens for characterization. Two of the virgin blends were tested for possible compatibilization using a styrene-ethylene-butylene-styrene (SEBS) block copolymer. In addition, six blends of post-consumer resins (PCRs) of HDPE and PET were included in this work for comparison. The moduli of the virgin blends showed positive deviation from those expected from the rule of mixtures. The synergism of the composite moduli can be explained partly by a Poisson's effect. Yield strengths of the blends molded at low injection chamber temperatures (200sp°, 230sp°, and 250sp°C) followed the rule of mixtures well, because PET filaments found in the composites had very high length to diameter ratios. When the injection chamber temperature was above the PET melting point (˜254sp°C), PET filaments were found to break down into particles, and the yield strengths of the blends coincided with the values expected from the inverse rule of mixtures. Impact strengths of the virgin blends were much less than that of a HDPE homopolymer due to poor interfacial bonding between HDPE and PET. Compatibilization appeared to be advantageous since it dramatically improved the impact strength of the virgin blends. SEM micrographs of impact fractured surfaces revealed that the improved adhesion from compatibilization and the presence of numerous uniaxially aligned PET filaments in the HDPE substrate can account for the significant increases in fracture resistance of the compatibilized blends. Mechanical performance of the PCRs was inferior to that of the virgin blends. Aside from polymer degradation and contamination due to repeated processing and handling, absence of PET filaments and interfacial bonding could be

  11. 上海石化碳四资源利用现状及发展探讨%Discussion on Utilization and Development of C_4 Hydrocarbon Resources in SINOPEC Shanghai Petrochemical Company Limited

    Institute of Scientific and Technical Information of China (English)

    张彩娟; 秦朝晖; 周欢华

    2012-01-01

    The sources,compositions,separation process and utilization of C4 hydroacarbon in SINOPEC Shanghai Petrochemical Company Limited were analyzed.For the compositions in C4 hydrocarbon which were by-products of refining and chemical plants and were not utilized rationally,proposal was raised to integrate the surplus C4 resources and build a light hydrocarbon aromatization plant to produce aromatics.And for the problem of comprehensive utilization of C4 hydrocarbon in capacity expansion project of 1# ethylene plant,proposals were raised on adopting combining process of synthesizing MTBE through etherification of isobutylene-producing high purified isobutylene through MTBE cracking,and process of producing methyl-ethyl-ketone from butylene by hydration and hydrogenaion.Meanwhile,proposals were raised on developing down-stream products of butadiene and building a synthetic rubber production plant.%分析了中国石化上海石油化工股份有限公司C4烃的来源、组成、分离工艺和利用途径;针对炼油系统和化工系统副产的C4烃中未被合理利用的组分,提出了整合剩余C4资源,建设一套轻烃芳构化生产芳烃装置的建议;针对1#乙烯装置扩能改造工程C4烃综合利用问题,提出了采用异丁烯醚化合成甲基叔丁基醚(MTBE)-MTBE裂解制高纯异丁烯组合工艺、正丁烯水合脱氢制甲乙酮工艺等建议,同时提出了发展丁二烯下游产品,建设一套生产合成橡胶装置的设想。

  12. 聚酯型水性紫外光固化聚氨酯的制备与性能%Preparation and properties of water-borne UV-curing polyester polyurethane

    Institute of Scientific and Technical Information of China (English)

    石耀东; 魏燕彦; 张颖颖; 沈泰龙; 唐洁珍

    2013-01-01

    合成了以聚己二酸丁二醇酯二元醇、聚己内酯二元醇(PCL)、聚碳酸酯二元醇(PCDL)为软段的水性紫外光固化聚氨酯树脂,通过红外光谱、乳液粒径、稳定性以及涂膜力学、耐水、耐溶剂性测试研究了软段类型、软段含量和交联剂对合成的乳液和涂膜性能的影响.通过调整分子结构,得到了粒径<30 nm的乳液,其储存稳定期> 12个月,冻融稳定性>5个循环.涂膜的硬度5H且180°对折无裂痕,抗划伤性好,耐水和溶剂性能优良,PCL和PCDL型树脂的涂膜耐丙酮擦拭35次以上,在木材、玻璃和塑料表面有很好的应用效果.%The water-borne UV-curing polyurethanes with poly (butylene adipate),polycaprolactone diol (PCL) and polycarbonate-diol (PCDL) as their soft segments were synthesized.The effects of soft segment,soft segment content and crosslinking agent on the properties of synthesized emulsion and film were investigated by their FT-IR spectra and and the testings of emulsion particle size and stability,mechanical properties,water resistance and solvent resistance of coatings.The emulsion with particle size < 30 nm was obtained by adjusting the molecular structure.The storage stability of emulsion was longer than 12 months and freeze-thaw stability was longer than 5 cycles.The coating hardness was 5H and no cracks after 180° folding.The coatings had good resistance of scratching,water and solvent.The resistance of acetone wipping of PCL and PCDL resin matrix coatings were more than 35 times.The coatings had a good application results on wood,glass and plastic surface.

  13. Surface science studies of thermal- and electron-induced reactions on metal and semiconductor surfaces

    Science.gov (United States)

    Tsai, Yi-Li

    The chemisorption of alkenes (ethylene, propylene, and butylene isomers) was systematically investigated on Pt(111) and the (2x2)Sn/Pt(111) and (sqrt3 xsqrt3)R30sp°Sn/Pt(111) surface alloys using temperature programmed desorption (TPD), Auger electron spectroscopy (AES) and low energy electron diffraction (LEED). Alloying Sn with Pt decreases the adsorption bond strength and decomposition of alkenes. Sn site-blocking within the alloy layer may play a key role in the chemistry of these surface alloys. The importance of pure Pt 3-fold sites and adjacent pure Pt 3-fold sites was proposed. Electrons for electron-induced dissociation (EID) of cycloalkane (C5-C8) multilayers was used to prepare monolayer coverages of adsorbed cycloalkyl intermediates on Pt(111) and two Sn/Pt(111) surface alloys. The subsequent thermal reaction products of these cycloalkyls include benzene and various cycloalkenes. We observed a high selectivity for desorption of these products on the Pt-Sn alloys. TPD results allowed us to conclude that the dominant mechanism for the formation of these surface alkyl groups is for the hydrocarbon fragment from EID to diffuse to the metal surface. The adsorption and desorption of several N-containing molecules for the growth of GaN, i.e., NHsb3, monomethylamine (MMA), dimethylamine (DMA) and trimethylamine (TMA), were investigated on the GaAs(100)-(4x6) surface under UHV conditions. TPD and AES results indicate essentially reversible adsorption for all and no GaN is formed by thermal activation. The desorption activation energies, and adsorption energies, are 19, 22, 24 and 23.5 kcal/mol for NHsb3, MMA, DMA and TMA, respectively. These similar energies indicate that all of these precursors chemisorbed via a weak dative bond between the N lone pair and an empty orbital on Ga sites. EID of MMA was also explored briefly. Low energy electrons (50 eV, 1 ×10sp{15}electrons/cmsp2) dissociate MMA, giving a large yield of Hsb2\\ and\\ NHsb3 desorption, but little

  14. New results of studying of the Devonian shale formation in the Volga-Ural region

    Science.gov (United States)

    Plotnikova, Irina; Pronin, Nikita; Morozov, Vladimir; Nosova, Fidania

    2015-04-01

    matter). Organic matter is characteristic mainly of the most siliceous formations. In "pure" carbonates, which are represented by micro-layers with different capacities, OM is not observed at all or its content is quite low. We found a connection between the type of organic matter and the composition of adsorbed gas. The study of adsorbed gases show the following: all samples have increased, high and abnormally high concentration of selected gases. Their common characteristic is that the gases are heavy, fatty, and have low methane content and hydrocarbons of unsaturated series (ethylene, propylene and butylene). Heavy hydrocarbons of saturated series are dominating, their share is changing irregularly in the homologous series. The use of aromatic carotenoids and alkyl toluenes can restore paleo facies conditions of sedimentation of the Domanik strata and paleo geodynamics of the part passive continental margin of the Baltica Late-Proterozoic continent.

  15. Effect of Straw Fiber Modification on Properties for Wheat Straw Fiber/PBS Composite%纤维改性对小麦秸秆纤维/PBS复合材料性能的影响

    Institute of Scientific and Technical Information of China (English)

    强琪; 张敏; 徐丹; 何文清; 宋吉青

    2013-01-01

    利用NaOH对小麦秸秆纤维进行处理,同时采用了不同的蒸煮助剂和改性剂,以改变纤维自身物理性能及其表面化学性质.将改性纤维与聚丁二酸丁二醇酯(PBS)共混,制备了秸秆纤维/PBS复合材料,并通过X射线能谱仪(EDS)、X射线衍射仪(XRD)和扫描电子显微镜(SEM)对改性前后的纤维进行了分析和观测,研究分析了助剂和改性剂对复合材料性能的影响.结果表明:秸秆纤维经NaOH/4%Na2SO3处理,以及碱处理纤维经钛酸酯偶联剂NDZ201、环氧树脂E44改性,所得纤维增强复合材料的性能较为优异.%Wheat straw fiber was treated with NaOH, meanwhile different additives and modifiers were used to alter the physical properties and surface chemical properties of wheat straw fiber, and the composites were prepared through the blending between the fibers and poly (butylene succinate) (PBS). Through analysis and observation of modified fibers by energy disperse spectroscopy (EDS), X-ray diffraction (XRD) and scanning electron microscopy (SEM), the effects of type and addition for additives and modifies on the properties of straw fiber and the straw fiber/PBS composites were studied. The results show that the property of the composite is better when the raw fiber is treated by NaOH/4%Na2SO3, and the NaOH treated fiber is modified by NOZ201 or E44.

  16. Study on Impact of Modified Wheat Straw Fibers on PBS Composites Properties%改性小麦秸秆纤维对PBS复合材料性能的影响研究

    Institute of Scientific and Technical Information of China (English)

    强琪; 张敏; 徐丹; 邱建辉

    2012-01-01

    Wheat straw fiber was treated by NaOH,on this basis,the Na 2 S 2 O 4 and coupling agents (KH550,KH560) were used to modify the fiber,then the wheat straw fiber/PBS composites were prepared through the blending with poly(butylene succinate) (PBS).The effects of addition of Na2S2O4,and modification of KH550 and KH560 after NaOH treatment on the properties of the straw fiber/PBS composites were studied.Energy disperse spectroscopy (EDS) ,X-ray diffraction and SEM were used to characterize and observe the modified fibers and composites before and after modification.The results indicated that the properties of the composite would be the best when the fiber was treated by NaOH-3% Na2S2O4,compared with KH550,the mechanical properties of composite modified by KH560 could been improved more effectively,and the properties would be the best when the addition of KH560 was 2%.%采用NaOH对小麦秸秆纤维进行处理,在此基础上使用蒸煮助剂Na2S2O4和偶联剂(KH550、KH560)改性秸秆纤维,并将其分别与聚丁二酸丁二醇酯(PBS)共混,制备了秸秆纤维/PBS复合材料.研究了NaOH处理中Na2S2O4的添加以及NaOH处理后KH550、KH560的改性对复合材料性能的影响.采用EDS、WXRD和SEM对改性前后的纤维及复合材料分别进行了分析和观测.研究结果表明:NaOH同3% Na2S2O4混合处理得到的复合材料的性能最好,KH560较KH550更能有效地改善复合材料的力学性能,当KH560质量分数为2%时,复合材料的力学性能最好.

  17. Leveraging material properties in fluorescence anion sensor arrays: a general approach.

    Science.gov (United States)

    Anzenbacher, Pavel; Liu, Yuanli; Palacios, Manuel A; Minami, Tsuyoshi; Wang, Zhuo; Nishiyabu, Ryuhei

    2013-06-24

    As the demand for probes suitable for sensor development increases, investigation of approaches that utilize known successful receptors gains in general importance. This study describes a two-prong approach that can be used as a guide to developing sensors from known receptors. First, the conversion of a simple receptor, calix[4]pyrrole, into a fluorescent probe to establish a ratiometric signal is described. Secondly, the sensors that employ an output from a single ratiometric calix[4]pyrrole probe are fabricated by using poly(ether-urethane) hydrogel copolymers. These hydrogels are designed to absorb, internalize and transport aqueous electrolytes. A sensor array of ten different poly(ether-urethane) matrices with varying comonomer proportions were doped with a single probe and were exposed to eight different anions: acetate, benzoate, fluoride, chloride, phosphate, pyrophosphate, hydrogen sulfide, and cyanide, eight urine samples and anti-inflammatory drugs (NSAIDs). The poly(ether-urethane) matrices comprise different proportions of anion-binding urethane moieties and different hydrophilicity given by the ratio between ethylene glycol ether and butylene glycol ether. This diversity in the hydration behavior provides different environment polarity, in which the recognition and self-assembly processes display enough diverse behavior to allow for unique response of the probe to the analytes. Furthermore, a single probe is shown to recognize eight different aqueous anions and eight urine samples when embedded in ten different polyurethanes in an array that displays 100 % classification accuracy. To demonstrate the potential of the concept for quantitative studies, an estimation of non-steroidal anti-inflammatory drugs ibuprofen and diclofenac in water and in saliva was performed. A limit of detection of 0.1 ppm and a dynamic range of 0.1-0.6 and 0.05-60 ppm was observed, respectively. Given the general difficulty of chemosensors to recognize aqueous anions

  18. 油溶性聚醚的制备及其抗氧化性能考察%PREARATION AND ANTIOXIDANT CHARACTERISTICS OF OIL-SOLUCLE POLYETHER

    Institute of Scientific and Technical Information of China (English)

    程亮; 李洪伟; 孔令杰; 张东恒

    2014-01-01

    以氢氧化钾作为催化剂,环氧丙烷与环氧丁烷共聚制备了分别符合黏度级别 OSP-18,OSP-46, OSP-150要求的油溶性聚醚,并通过红外光谱(IR)、核磁共振(NMR)和凝胶渗透色谱(GPC)对其进行表征。利用旋转氧弹测试方法考察了油溶性聚醚的抗氧化性能,结果表明油溶性聚醚本身的抗氧化性能较差。通过考察不同抗氧剂与油溶性聚醚的互配性,开发了α-苯胺与氨基甲酸酯组成的复合抗氧剂,该复合抗氧剂与油溶性聚醚有较好的互配性,可使油溶性聚醚的旋转氧弹时间达到1200 min,复合抗氧剂可使油溶性聚醚在不同配方体系中得到应用。%Oil-soluble polyether (OSP)was prepared by the copolymerization of propylene oxide and butylene oxide using KOH as a catalyst.The viscosity grades of the prepared oil-soluble polyether are OSP-18,OSP-46,OSP-150,respectively.The structures of the products were defined by means of infra-red spectroscopy (IR),nuclear magnetic resonance (NMR)and gel permeation chromatography (GPC). The anti-oxidation performance of OSPs were investigated by rotary oxygen bomb test method (ROBT).The results indicate that the oil-soluble polyether is poor in anti-oxidation with short induc-tion period.However,the performance of the oil-soluble polyether is greatly improved by addition of the composite antioxidant,composed of α-aniline (AOA-4 )and carbamate (AOL-1 ). The ROBT can reach to 1 200 minutes.The performance of this composite antioxidant makes OSP the best application in different formulations.

  19. PP/Talc/MA-SEBS复合材料的力学性能研究%The Mechanical Properties of PP/Talc/MA-SEBS Composite

    Institute of Scientific and Technical Information of China (English)

    谢晓春

    2011-01-01

    PP/Talc composites compatibilized by MA-SEBS(maleic anhydride grafted styrene-(ethylene-co-butylene)-styrene copolymer) were prepared by melt extrusion, followed by injection molding. The effects of Talc and MA-SEBS on mechanical properties of PP/Talc/MA-SEBS composites were systematically investigated. The results indicated that Talc mixing into PP could obviously improve the impact strength of PP at room temperature. After the entry of MA-SEBS to the PP/Talc composites, the impact strength increased even more. MA-SEBS acted as a toughening agent as well as a compatilizer, enhancing the toughening effect of Talc. The rigid Talc particles made the flexural strength increase markedly, and the flexural moduls go up with the increase of Talc content; and elastomer MA-SEBS got the flexural performance of composites obviously deteriorated. Talc had no bad effect on the PP tensile properties; if adding Talc and MA-SEBS at the same time,the tensile strength would go down, and tend to decrease with increasing MA-SEBS content in the composites.%选用MA-SEBS为增容剂,制备了PP/滑石粉(Talc)/MA-SEBS复合材料,研究了Talc和MA-SEBS的含量对复合材料力学性能的影响.结果表明,单纯加入一定量Talc可以明显提高PP冲击强度,再加入MA-SEBs后,复合材料的冲击强度进一步增加.MA-SEBS除了作为相容剂.也充当增韧剂.刚性粒子Talc使材料的弯曲强度明显增大,弯曲模量随Talc含量增加而增大;而弹性体MA-SEBS使材料弯曲性能明显变差.单纯加入Talc对PP的拉伸性能无负面影响;若同时加入Tak和MA-SEBS,材料的拉伸强度明显下降,且MA-SEBS含量越大降幅越大.

  20. Adjustment of surface chemical and physical properties with functionalized polymers to control cell adhesion

    Science.gov (United States)

    Zhou, Zhaoli

    Cell-surface interaction is crucial in many cellular functions such as movement, growth, differentiation, proliferation and survival. In the present work, we have developed several strategies to design and prepare synthetic polymeric materials with selected cues to control cell attachment. To promote neuronal cell adhesion on the surfaces, biocompatible, non-adhesive PEG-based materials were modified with neurotransmitter acetylcholine functionalities to produce hydrogels with a range of porous structures, swollen states, and mechanical strengths. Mice hippocampal cells cultured on the hydrogels showed differences in number, length of processes and exhibited different survival rates, thereby highlighting the importance of chemical composition and structure in biomaterials. Similar strategies were used to prepare polymer brushes to assess how topographical cues influence neuronal cell behaviors. The brushes were prepared using the "grown from" method through surface-initiated atom transfer radical polymerization (SI-ATRP) reactions and further patterned via UV photolithography. Protein absorption tests and hippocampal neuronal cell culture of the brush patterns showed that both protein and neuronal cells can adhere to the patterns and therefore can be guided by the patterns at certain length scales. We also prepared functional polymers to discourage attachment of undesirable cells on the surfaces. For example, we synthesized PEG-perfluorinated alkyl amphiphilic surfactants to modify polystyrene-block-poly(ethylene-ran-butylene)- block-polyisoprene (SEBI or K3) triblock copolymers for marine antifouling/fouling release surface coatings. Initial results showed that the polymer coated surfaces can facilitate removal of Ulva sporelings on the surfaces. In addition, we prepared both bioactive and dual functional biopassive/bioactive antimicrobial coatings based on SEBI polymers. Incubating the polymer coated surfaces with gram-positive bacteria (S. aureus), gram

  1. PBS/EVOH共混物制备与性能研究%Preparation and Properties of Polybutylene Succinate/Ethylene-Vinyl Alcohol Blends

    Institute of Scientific and Technical Information of China (English)

    赵芸芳

    2012-01-01

    利用熔融共混法制备了综合性能优良的聚丁二酸丁二醇酯/乙烯-乙烯醇共聚物( PBS/EVOH)共混物,并通过扫描电子显微镜、傅立叶转变红外光谱( FTIR)仪、万能试验机以及差示扫描量热分析仪分别研究了共混体系的微观形态、两相间的作用情况、力学性能以及热性能.结果表明,共混体系为两相“海-岛”结构,分散相以“球状”均匀地分布于连续相中,且两相界面结合比较好;FTIR结果证实了PBS与EVOH之间存在强烈的氢键作用,且氢键作用降低了PBS结晶度,从而可以加快PBS的降解过程.PBS/EVOH共混物可用于制造可降解的包装薄膜材料.%Poly butylenes succinate / ethyTene-vinyl alcohol ( PBS / EVOH ) blends were prepared by melt blending.The morphology, interaction between two phase, mechanical and thermal properties of the composites were investigated via scanning electron microscopy ( SEM X fourier transform infrared chromatograph ( FTIR )> universal testing machine and differential scanning calorimetry ( DSC) respectively.The result showed that the composite was two-phase "sea-island" structure, the interaction between the sphere dispersed phase and continuous phase was good.FTIR analysis verified the existence of H-bonding between PBS and EVOH, and H-bonding reduced the crystallization of PBS, so accelerated the degradation of PBS.PBS / EVOH blends could be used to make biodegradable packing film.

  2. Final report on the safety assessment of Arnica montana extract and Arnica montana.

    Science.gov (United States)

    2001-01-01

    Arnica Montana Extract is an extract of dried flowerheads of the plant, Arnica montana. Arnica Montana is a generic term used to describe a plant material derived from the dried flowers, roots, or rhizomes of A. montana. Common names for A. montana include leopard's bane, mountain tobacco, mountain snuff, and wolf's bane. Two techniques for preparing Arnica Montana Extract are hydroalcoholic maceration and gentle disintegration in soybean oil. Propylene glycol and butylene glycol extractions were also reported. The composition of these extracts can include fatty acids, especially palmitic, linoleic, myristic, and linolenic acids, essential oil, triterpenic alcohols, sesquiterpene lactones, sugars, phytosterols, phenol acids, tannins, choline, inulin, phulin, arnicin, flavonoids, carotenoids, coumarins, and heavy metals. The components present in these extracts are dependent on where the plant is grown. Arnica Montana Extract was reported to be used in almost 100 cosmetic formulations across a wide range of product types, whereas Arnica Montana was reported only once. Extractions of Arnica Montana were tested and found not toxic in acute toxicity tests in rabbits, mice, and rats; they were not irritating, sensitizing, or phototoxic to mouse or guinea pig skin; and they did not produce significant ocular irritation. In an Ames test, an extract of A. montana was mutagenic, possibly related to the flavenoid content of the extract. No carcinogenicity or reproductive/developmental toxicity data were available. Clinical tests of extractions failed to elicit irritation or sensitization, yet Arnica dermatitis, a delayed type IV allergy, is reported in individuals who handle arnica flowers and may be caused by sesquiterpene lactones found in the flowers. Ingestion of A. montana-containing products has induced severe gastroenteritis, nervousness, accelerated heart rate, muscular weakness, and death. Absent any basis for concluding that data on one member of a botanical

  3. Propriedades mecânicas e morfologia de uma blenda polimérica de PP/HIPS compatibilizada com SEBS Mechanical properties and morphology of a PP/HIPS polymer blend compatibilized with SEBS

    Directory of Open Access Journals (Sweden)

    Tomás J. A. de Mélo

    2000-06-01

    Full Text Available Neste trabalho o efeito da adição de 2 a 7% em peso de um copolímero tribloco estireno-b-etileno-co-butileno-b-estireno (SEBS em uma blenda polipropileno/poliestireno de alto impacto (PP/HIPS 70:30 foi determinado. As propriedades em tração e impacto, temperatura de amolecimento Vicat e morfologia da blenda PP/HIPS (70:30 em função da concentração de SEBS foram determinadas. As blendas foram processadas em extrusora dupla-rosca contra-rotativa interpenetrante e as amostras moldadas por compressão. Os resultados mostraram que, embora a adição do SEBS tenha promovido um aumento muito leve na resistência tênsil e no módulo elástico, observou-se um expressivo aumento no alongamento na ruptura e na resistência ao impacto das blendas; a temperatura Vicat das blendas foi superior à do HIPS e que a adição do SEBS promoveu uma redução significativa do tamanho de partícula, indicando que o SEBS exerceu um efeito emulsificante e estabilizador na morfologia das blendas investigadas. Resultados otimizados foram obtidos para a composição contendo 5% de SEBS, o que foi atribuido à uma maior compatibilidade entre as fases.In this work the effect of a 2-7% w/w styrene-b-ethylene-co-butylene-b-styrene triblock copolymer (SEBS addition on the properties of a 70:30 polypropylene/high impact polystyrene (PP/HIPS polymer blend was investigated. Tensile and impact properties, the Vicat temperature and blend morphology were determined as a function of SEBS content. Processing was carried out in a twin-screw intermeshing counter-rotating extruder and the samples were compression moulded. Our results indicate that the SEBS addition, albeit promoting very slight increases on tensile strenght and modulus, led to increases on the elongation at break and impact strenght of the blends, and the Vicat temperature of the blends was higher than that of HIPS. The SEM analysis showed that SEBS addition promotes a significant reduction on particle size

  4. Alkaline degradation studies of anion exchange polymers to enable new membrane designs

    Science.gov (United States)

    Nunez, Sean Andrew

    Current performance targets for anion-exchange membrane (AEM) fuel cells call for greater than 95% alkaline stability for 5000 hours at temperatures up to 120 °C. Using this target temperature of 120 °C, an incisive 1H NMR-based alkaline degradation method to identify the degradation products of n-alkyl spacer tetraalkylammonium cations in various AEM polymers and small molecule analogs. Herein, the degradation mechanisms and rates of benzyltrimethylammonium-, n-alkyl interstitial spacer- and n-alkyl terminal pendant-cations are studied on several architectures. These findings demonstrate that benzyltrimethylammonium- and n-alkyl terminal pendant cations are more labile than an n-alkyl interstitial spacer cation and conclude that Hofmann elimination is not the predominant mechanism of alkaline degradation. Additionally, the alkaline stability of an n-alkyl interstitial spacer cation is enhanced when combined with an n-alkyl terminal pendant. Interestingly, at 120 °C, an inverse trend was found in the overall alkaline stability of AEM poly(styrene) and AEM poly(phenylene oxide) samples than was previously shown at 80 °C. Successive small molecule studies suggest that at 120 °C, an anion-induced 1,4-elimination degradation mechanism may be activated on styrenic AEM polymers bearing an acidic alpha-hydrogen. In addition, an ATR-FTIR based method was developed to assess the alkaline stability of solid membranes and any added resistance to degradation that may be due to differential solubilities and phase separation. To increase the stability of anion exchange membranes, Oshima magnesate--halogen exchange was demonstrated as a method for the synthesis of new anion exchange membranes that typically fail in the presence of organolithium or Grignard reagents alone. This new chemistry, applied to non-resinous polymers for the first time, proved effective for the n-akyl interstitial spacer functionalization of poly(phenylene oxide) and poly(styrene- co-ethylene-co-butylene

  5. Efeito da adição de diferentes copolímeros em blendas HDPE/HIPS pós-consumo: morfologia de fases e propriedades térmicas The effect of different block copolymers on post consumer HDPE/HIPS Blends: phase morphology and thermal properties

    Directory of Open Access Journals (Sweden)

    Igor S. B. Perez

    2008-09-01

    Full Text Available Blendas de poliolefinas/HIPS têm sido exploradas para obter filmes especiais com determinadas propriedades desejadas, tornando imperativo desenvolver vários estudos para um melhor conhecimento do comportamento desses materiais. Neste trabalho, efeitos da adição dos copolímeros comerciais de estireno-butadieno multibloco (SBS e de estireno-(etileno-co-butileno-estireno (SEBS tribloco linear em blendas pós-consumo de HDPE e HIPS são reportados. A diminuição nas dimensões da microfase dispersa, aliada à rugosidade superficial da fase HDPE após extração seletiva do HIPS, independentemente de a fase matriz ser HIPS ou HDPE, mostraram mais eficiência do SEBS como modificador interfacial de tensão ou como surfactante entre os diferentes domínios quando comparado com o SBS. Os resultados das caracterizações térmicas, por exemplo, menor Tm e menor grau de cristalinidade do HDPE, e maior Tg do poliestireno na presença de SEBS corroboraram esta conclusão, como será discutido posteriormente.Blending of post-consumer polyolefins/HIPS has been exploited for obtaining special films with a desired set of properties, which has required studies to understand the behavior of these materials. In this work the effects of commercial multiblock styrene-butadiene (SBS and linear triblock styrene-(ethylene-co-butylene-styrene (SEBS copolymers in blends of post-consumer high density polyethylene (HDPE and HIPS are reported. Thermal properties and phase morphology were comparatively analyzed for the additives aiming at verifying possible correlations between them. Decreased dimensions of the minor micro phase along with HDPE surface roughness after HIPS selective extraction, independently of the matrix being HIPS or HDPE, showed better effectiveness for SEBS as interfacial tension modifier or as surfactant at the different domains interface when compared with SBS. The results of thermal characterizations, e.g. lower HDPE melting temperature, lower

  6. Effect of anti-inflamentation extracts from Korean traditional medicinal herb

    Directory of Open Access Journals (Sweden)

    Zhang Xiaowan

    2014-09-01

    Full Text Available Five Mix Plant Extracts according to different extraction solvents were assessed for its cell viability and anti-inflammatory activity by in vitro methods. The single plant extract was extracted with 70% ethanol(EtOH and the mix plants(C.kousa, R.multiflora, T.nucifera, M.basjoo and S.glabra were extracted with EtOH 30%, 70%; Butylene Glycol(BG 30%, 70%; Propylene Glycol(PG 30%, 70%; Distilled Water(D.W. Cell viability was measured using the Micro culture tetrazolium (MTT assay method and Human fibroblast cells, CCD 1102 KERTr were used. The plant extracts with the maximum concentration that none toxic to the cells were evaluated for anti-inflammatory activity. Anti-inflammatory activity was evaluated using lipoxygenase inhibition assay method. A dose response curve was plotted to determine the IC50 values. Results showed that, at the 5 kinds of single plant extracts by 70% EtOH extraction solvent, it showed the IC50 was 280ug/ml of S1, 370ug/ml of S2, 380ug/ml of S3, 170ug/ml of S4 and 190ug/ml of S5. At the mix plant extracts by 7 kinds of extraction solvents (70%, 30% EtOH; 70%, 30% BG; 70%, 30% PG; D.W, it showed the IC50 was 140ug/ml of M E70, 140ug/ml of M E30, 120ug/ml of M BG70, 110ug/ml of M BG30, 120ug/ml of M PG70, 136ug/ml of M PG30 and 120ug/ml of M D.W. From the results, it is concluded that when these five plants mixed before extraction, it will extract more active ingredients with anti-inflammatory effects. Further study we will analyzing plants effective single compound using high performance liquid chromatography (HPLC profiling and progressing the experiments in vivo.

  7. Environmental effects of poly(phenylene ether) blends after long-term exposure to potable hot water

    Science.gov (United States)

    Maclean, Steven

    In recent years, engineering thermoplastic resins have been contemplated for use in a variety pressurized fluid handling components such as potable water delivery pipes, fitting and valves. In this research, rigid blends of glassy poly(phenylene ether) (PPE) polymer are studied to assess their suitability in long-term, potable, hot water environments. Three distinct PPE-based model compounds were prepared for this research: (i) a 50/50 blend of PPE and high impact polystyrene (HIPS); (ii) a 50/50 blend of PPE and HIPS with the inclusion of an anti-oxidant package and; (iii) a blend consisting of capped PPE, crystal polystyrene and styrene-ethyelene-butylene-styrene (SEBS) rubber. A fourth engineering thermoplastic, namely bisphenol-A polysulfone (PSU), was incorporated into the study as a benchmark material due to its proven reliability in hot water applications. Aging experiments were carried out for 8,000 hours in an 80°C water bath and an 80°C convection oven to characterize physical property retention and degradation mechanisms in each material. During water bath immersion, excessive, non-Fickian water diffusion occurred in both PPE/HIPS blends which led to water clustering and disc shaped microcavities on the order of 50 to 100 mum in diameter. These voids in the bulk caused appreciable losses in tensile elongation and fatigue resistance. The capped PPE/PS/SEBS blend, however, managed water uptake more effectively and its chemistry deterred water clustering. With further improvements to the formulation, such as larger rubber domains or an alternative impact modifier, the capped PPE blend may be able to offer physical property retention equal to that of PSU. With the exception of slight craze formation at sharp specimen edges during hot water immersion, the PSU material proved to be an exceptional material candidate throughout the entire experimentation. Surprisingly long-term hot water exposure did not cause gross chemical degradation in any of the materials

  8. Processing and characterization of solid and microcellular biobased and biodegradable PHBV-based polymer blends and composites

    Science.gov (United States)

    Javadi, Alireza

    Petroleum-based polymers have made a significant contribution to human society due to their extraordinary adaptability and processability. However, due to the wide-spread application of plastics over the past few decades, there are growing concerns over depleting fossil resources and the undesirable environmental impact of plastics. Most of the petroleum-based plastics are non-biodegradable and thus will be disposed in landfills. Inappropriate disposal of plastics may also become a potential threat to the environment. Many approaches, such as efficient plastics waste management and replacing petroleum-based plastics with biodegradable materials obtained from renewable resources, have been put forth to overcome these problems. Plastics waste management is at its beginning stages of development which is also more expensive than expected. Thus, there is a growing interest in developing sustainable biobased and biodegradable materials produced from renewable resources such as plants and crops, which can offer comparable performance with additional advantages, such as biodegradability, biocompatibility, and reducing the carbon footprint. Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) is one of the most promising biobased and biodegradable polymers, In fact many petroleum based polymers such as poly(propylene) (PP) can be potentially replaced by PHBV because of the similarity in their properties. Despite PHBV's attractive properties, there are many drawbacks such as high cost, brittleness, and thermal instability, which hamper the widespread usage of this specific polymer. The goals of this study are to investigate various strategies to address these drawbacks, including blending with other biodegradable polymers such as poly (butylene adipate-coterephthalate) (PBAT) or fillers (e.g., coir fiber, recycled wood fiber, and nanofillers) and use of novel processing technologies such as microcellular injection molding technique. Microcellular injection molding technique

  9. Defeating anisotropy in material extrusion 3D printing via materials development

    Science.gov (United States)

    Torrado Perez, Angel Ramon

    ABS, UHMWPE (Ultra High Molecular Weight Polyethylene) and SEBS (Styrene Ethylene Butylene Styrene) were further examined due to the potential they demonstrated as low anisotropic materials in terms of strength. Also, the geometrical influence of different standard tensile specimens was studied. The development of materials that lead to lowered anisotropy on the strength of 3D printed parts has been successfully demonstrated, and alternative methodologies for the evaluation of anisotropic characteristics has been proposed as well. The present work shows the beginning to a better understanding of the mechanics taking place during the fusion of deposited material in MEAM.

  10. Synthesis of High Solid Content Polyurethane Dispersion Adhesive by Pellet Process%粒料法合成高固含量聚氨酯分散体胶粘剂

    Institute of Scientific and Technical Information of China (English)

    贺丽娜; 孙东成

    2012-01-01

    Polyurethane inomer was prepared by isophorone diisocyanate(IPDI) and 1,4-butanediol(BG)as hard segments,poly(1,4-butylene adipate glycol)(PBA) with an average molecular weight of 3000 as soft segments,polyether diol containing sulfonate(SPPG) as hydrophilic monomer in soft segment,and dibutyltin dilaurate(DBTDL) as catalysts through bulk polymerization.Polyurethane dispersions(PUDs) adhesive with a solid content of 50% was synthesized by granulation,dissolution in acetone,dispersion in water,distillation of acetone of polymerization.The effect of hard segment content and molecular weight on mean particle size and particle distribution,thermodynamics performance of cast films,and adhesive performance was researched in this paper.The results show that the maximum I-Peel strength and T-Peel strength is 6N/mm and 10.24 N/mm,respectively and the cast films has good heat resitence.%以聚己二酸1,4-丁二醇酯(PBA-3000)为软段、异佛尔酮二异氰酸酯(IPDI)、1,4-丁二醇(BG)为硬段、聚醚二元醇磺酸盐(SPPG)作为亲水单体,采用本体聚合方法合成了聚氨酯离子聚合物。聚氨酯离子聚合物经造粒、丙酮溶解、水分散、去丙酮得到固含量为50%的高固含量聚氨酯分散体胶粘剂。研究了硬段含量、分子量对分散体平均粒径和粒径分布、胶膜的热学性能以及粘合性能的影响。聚氨酯分散体胶粘剂的最高初粘力为6N/mm,最高剥离强度为10.24 N/mm。

  11. Preparation of Two-Component Cationic Polyurethane Electrophoresis Paint and Optimization for the Electrophoresis Technology%双组分水性阴极聚氨酯电泳漆的制备及其工艺优化

    Institute of Scientific and Technical Information of China (English)

    曹玉阳; 吴元; 李再峰

    2013-01-01

    A queous hydroxyl-terminated cationic polyurethane resin which based on low relative molecular weight polymer diols,isophorone diisocyanate (IPDI) , methyldiethanolamine(MDEA)and 1,4-butylene glycol(BDO) were synthesized. The resin was mixed and dispersed with end-capped crosslinking agent which based on IPDI, MDEA, BDO and 2-butanone oxime(MEKO) ,then the obtained emulsion was electroplated. The influence of electrophoresis process parameters, the dosage of PPH cosolvent ,the types of low relative molecular weight polymer diols, the influence of nNCO/nOH on the appearance and performance of the PU film were investigated. The result showed that the excellent performance could be obtained under the condition of 60 V for the electrophoresis voltage,40 s for the electrophoresis time,the mass ratio at about 3. 0% for cosolvent PPH,PTMG-1000 as the soft segment and the nNC0/nOH ratio at 1.1.%以低聚物二元醇、异佛尔酮二异氰酸酯(IPDI)、N-甲基二乙醇胺(MDEA)和1,4-丁二醇(BDO)为主要原料制备了阳离子型端羟基聚氨酯树脂;再以IPDI、MDEA、BDO以及甲乙酮肟(MEKO)为主要原料制备了阳离子型端异氰酸酯固化剂,将树脂与固化剂混合、分散乳化后进行电泳成膜.考察了电泳工艺参数、助溶剂丙二醇苯醚(PPH)用量、低聚物二元醇种类、树脂与固化剂的nNCO/nOH对漆膜表观及性能的影响.结果表明,电泳电压为60 V,电泳时间为40 s,PPH质量分数为3.0%(相对于树脂),以聚四氢呋喃醚二醇(PTMG-1000)为二元醇组分,nNCO/nOH为1.1时,漆膜表现出较好的性能及表观.

  12. Reactivity of Benzophenone Ketyl Free Radicals in an Elongated Elastomer Film.

    Science.gov (United States)

    Levin, Peter P; Efremkin, Alexei F; Kasparov, Valery V; Khudyakov, Igor V

    2016-09-29

    The effect of polymer film elongation leading to the thinning of the film up to three times on the decay of transients was studied. Kinetics of benzophenone (B) triplet state (3)B* and ketyl free radical BH• in soft rubber poly(ethylene-co-butylene) (abbreviated as E) was investigated by nanosecond laser flash photolysis. We monitored decay kinetics of the triplet state of (3)B* and of BH• decay in the polymer cage and decay of BH• in the polymer bulk. The fast exponential decay of (3)B*(lifetime τT ≈ 200 ns) is accompanied by hydrogen atom abstraction from E with the formation of BH• and a polymer free radical R•. The decay of BH• in the polymer cage occurs during τc ≈ 1 μs. Cage recombination, in turn, was followed by a cross-termination of BH• in the polymer bulk (τb ≈ 100 μs under our conditions) and is characterized by a rate constant kb ≈ 10(8) M(-1) s(-1). We studied changes of rates of transients decay upon elongation (thinning) of E. Decay of (3)B* is practically independent of elongation of the film. Recombination of BH• in the solvent bulk occurs with a two times lower kb than in a nonelongated E. The decrease in kb is ascribed mainly to a lower fractional polymer free volume Vf in elongated E compared with that in nonelongated E. Dependencies of log10 kb versus [Formula: see text], where [Formula: see text] is the thickness of the film, turned out to be linear with a negative slope. At the same [Formula: see text] recombination proceeds slower in the elongated elastomer compared with the nonelongated elastomer. Cage effect increases twice as well due to a lower rate of radicals escape from the polymer cage in the elongated film. We observed relatively large effects of external magnetic field (B = 0.2T) on the kinetics of cage recombination and recombination in the polymer bulk. Magnetic field effect on recombination rates in the cage and in the solvent bulk does not depend on elongation.

  13. Water-enhanced solvation of organics

    Energy Technology Data Exchange (ETDEWEB)

    Lee, J.H.

    1993-07-01

    Water-enhanced solvation (WES) was explored for Lewis acid solutes in Lewis base organic solvents, to develop cheap extract regeneration processes. WES for solid solutes was determined from ratios of solubilities of solutes in water-sat. and low-water solvent; both were determined from solid-liquid equilibrium. Vapor-headspace analysis was used to determine solute activity coefficients as function of organic phase water concentration. WES magnitudes of volatile solutes were normalized, set equal to slope of log {gamma}{sub s} vs x{sub w}/x{sub s} curve. From graph shape {Delta}(log {gamma}{sub s}) represents relative change in solute activity coefficient. Solutes investigated by vapor-headspace analysis were acetic acid, propionic acid, ethanol, 1,2-propylene glycol, 2,3-butylene glycol. Monocarboxylic acids had largest decrease in activity coefficient with water addition followed by glycols and alcohols. Propionic acid in cyclohexanone showed greatest water-enhancement {Delta} (log {gamma}{sub acid})/{Delta}(x{sub w}/x{sub acid}) = {minus}0.25. In methylcyclohexanone, the decrease of the activity coefficient of propionic acid was {minus}0.19. Activity coefficient of propionic acid in methylcyclohexanone stopped decreasing once the water reached a 2:1 water to acid mole ratio, implying a stoichiometric relation between water, ketone, and acid. Except for 2,3-butanediol, activity coefficients of the solutes studied decreased monotonically with water content. Activity coefficient curves of ethanol, 1,2-propanediol and 2,3-butanediol did not level off at large water/solute mole ratio. Solutes investigated by solid-liquid equilibrium were citric acid, gallic acid, phenol, xylenols, 2-naphthol. Saturation concentration of citric acid in anhydrous butyl acetate increased from 0.0009 to 0.087 mol/L after 1.3 % (g/g) water co-dissolved into organic phase. Effect of water-enhanced solvation for citric acid is very large but very small for phenol and its derivatives.

  14. CBT/PA6共混物等温及非等温结晶动力学%Isothermal and non-isothermal crystallization kinetics of CBT/PA6 blends

    Institute of Scientific and Technical Information of China (English)

    董红星; 赵庆晨; 佟丽莉; 刘文婧; 张进; 杨晓光; 刘立佳; 张春红; 李峻青

    2015-01-01

    利用溶液共混法制备了尼龙6( PA6)/对苯二甲酸丁二醇酯( CBT)的共混物,研究了PA6和CBT/PA6体系粘度随温度的变化、结晶形态以及等温和非等温结晶动力学. 流变结果表明,CBT的加入可以明显降低PA6的粘度. DSC结果表明:等温结晶时,加入CBT后,PA6的Avrami指数n、t1/2、tmax均降低,结晶速率G提高;非等温结晶时,共混物的Jeziorny指数n有所降低,相比于PA6,结晶速率加快. POM结果表明:CBT的加入能有效地增加PA6的成核密度. 可见CBT有望成为PA6结晶过程促进剂.%This paper studied the blends that were produced by the way of solution mixing of nylon 6 ( PA6) and cyclic butylenes terephthalate ( CBT) , the viscosity of the PA6 and CBT/PA6 blends changing with temperature, the crystalline form, and the isothermal and non-isothermal crystallization kinetics. The rheological results showed that with the addition of CBT it could significantly reduce the viscosity of PA6. The DSC results showed that in iso-thermal crystallization the Avrami indices n, t1/2, tmax of PA6 were reduced while the crystallization rate G increased as the CBT was added into the blend. In non-isothermal crystallization, the blend's Jeziorny index n was reduced and comparing with PA6 the crystallization rate was faster. Based on the studies in this paper, CBT is expected to become an accelerator, which can effectively increase nucleation density of PA6.

  15. Chemical and enzymatic catalytic routes to polyesters and oligopeptides biobased materials

    Science.gov (United States)

    Zhu, Jianhui

    My Ph.D research focuses on the synthesis and property studies of different biobased materials, including polyesters, polyurethanes and oligopeptides. The first study describes the synthesis, crystal structure and physico-mechanical properties of a bio-based polyester prepared from 2,5-furandicarboxylic acid (FDCA) and 1,4-butanediol. Melt-polycondensation experiments were conducted by a two-stage polymerization using titanium tetraisopropoxide (Ti[OiPr] 4) as catalyst. Polymerization conditions (catalyst concentration, reaction time and 2nd stage reaction temperature) were varied to optimize poly(butylene furan dicarboxylate), PBF, molecular weight. A series of PBFs with different Mw were characterized by Differential Scanning Calorimetry (DSC), Thermogravimetric Analysis (TGA), Dynamic Mechanical Thermal Analysis (DMTA), X-Ray diffraction and tensile testing. Influence of molecular weight and melting/crystallization enthalpy on PBF material tensile properties was explored. Cold-drawing tensile tests at room temperature for PBF with Mw 16K to 27K showed a brittle-to-ductile transition. When Mw reaches 38K, the Young's Modulus of PBF remains above 900 MPa, and the elongation at break increases to above 1000%. The mechanical properties, thermal properties and crystal structures of PBF were similar to petroleum derived poly(butylenes terephthalate), PBT. Fiber diagrams of uniaxially stretched PBF films were collected, indexed, and the unit cell was determined as triclinic (a=4.78(3) A, b=6.03(5) A, c=12.3(1) A, alpha=110.1(2)°, beta=121.1(3)°, gamma=100.6(2)°). A crystal structure was derived from this data and final atomic coordinates are reported. We concluded that there is a close similarity of the PBF structure to PBT alpha- and beta-forms. In the second study, a biobased long chain polyester polyol (PC14-OH) was synthesized from o-hydroxytetradecanoic acid (o-HOC14) and 1,4-butanediol. The first section about polyester polyurethanes describes the synthesis

  16. PBT/CF导热复合材料的制备与研究%Preparation and Research of Thermally Conductive PBT/CF Composites

    Institute of Scientific and Technical Information of China (English)

    洪玉琢; 朱健; 冯正明; 戚嵘嵘

    2015-01-01

    为了提高聚对苯二甲酸丁二酯(PBT)的热导率,采用碳纤维(CF)作为导热填料,制备了PBT/CF复合材料,并研究了复合材料的热导率和力学性能等。结果表明,CF的加入能够显著提高PBT/CF复合材料的热导率,且热导率具有方向性,PBT/CF复合材料层内方向的热导率高于层间方向的热导率;当CF用量为50份时,PBT/CF复合材料的层内热导率和层间热导率分别为1.034 W/(m · K)和0.635 W/(m · K),相比于纯PBT的0.237 W/(m · K),分别提高了336%和168%;随CF用量的增加,复合材料的拉伸强度呈现先上升后降低的趋势,当CF用量为20份时,复合材料的拉伸强度达到最大值,为91.5 MPa,断裂伸长率逐渐降低;Lewis-Nielsen模型对PBT/CF复合材料热导率的模拟效果较好,可以预测不同CF用量时复合材料的热导率。%In order to improve the thermal conductivity of poly(butylene terephthalate)(PBT),carbon fiber(CF) was chosen as the conductive filler. PBT/CF composites were prepared,and the thermal conductivity,and the mechanical properties of the composites were researched. The results show that CF can enhance observably the thermal conductivity of PBT/CF composites,and the thermal conductivity is different in different direction. The in-plane and through-plane thermal conductivity is 1.034 W/(m · K) and 0.635 W/(m · K) with 50 phr CF,which is increased by 336%and 168%compared with the pure PBT. The tensile strength of PBT/CF composites first increases and then decreases with the increase of CF,the tensile strength is 91.5 MPa with 20 phr CF, reaching the maximum strength;the elongation at break decreases with the increase of CF. The Lewis-Nielsen model simulates thermal conductivity of the composites well and can be used to predicted the thermal conductivity well with different CF content.

  17. MA-SEBS对超高分子量聚乙烯/碳纳米管复合材料结晶和熔融行为的影响%Effect of MA-SEBS on crystallization and melting behavior of ultra high molecular weight polyethylene/carbon nanotube composites

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    以马来酸酐接枝SEBS (MA-SEBS)作相容剂,采用溶液共混的方法制备超高分子量聚乙烯(UHMWPE)/碳纳米管(CNTs)复合材料.熔融结晶的UHMWPE/CNT复合材料是将其熔体以20℃/分的速率降温结晶而成.采用差示扫描量热法(DSC)研究了以不同方式结晶制备的UHMWPE/CNT复合材料的结晶和熔融行为.结果表明UHMWPE/CNT复合材料中UHMWPE相在溶液态结晶比在熔融态结晶形成的晶片厚,因而表现出更高的熔点(Tm)和结晶度(Xc).随着CNTs含量增加,UHMWPE/CNT复合材料中UHMWPE相的结晶温度(Tc)趋于提高.而且MA-SEBS的加入降低了UHMWPE/CNT复合材料中UHMWPE相的Tm 和 Tc. 此外UHMWPE/CNT复合材料中UHMWPE相的结晶速率随CNTs的引入而提高; MA-SEBS起相容剂的作用,改善了CNTs在UHMWPE基体中的分散性,使UHMWPE相的结晶速率进一步提高.%Ultra-high molecular weight polyethylene (UHMWPE) is filled with carbon nano-tubes (CNTs) by solution in the presence of maleic anhydride grafted styrene-(ethylene-co-butylene)-styrene copolymer (MA-SEBS) as a compatibilizer. The UHMWPE/CNT composites crystallized in melting state were prepared at a cooling rate of 20 ℃ min-1. The melting and crystallization behaviors of UHMWPE/CNT composites were investigated by differential scanning calorimetry. The results showed that Tm and Xc of UHMWPE/CNT composites crystallized in solution state are higher than those in melting state due to the larger crystalline lamellar thickness. Tc of UHMWPE/CNT composites tends to shift to higher temperature region with increasing CNTs content in the composites. Tm and Tc of UHMWPE phase in UHMWPE/CNT composites decrease with the addition of MA-SEBS. Moreover, the crystallization rate of UHMWPE phase in UHMWPE/CNT composite is accelerated due to the introduction of CNTs. MA-SEBS acts as compatilizer, enhances the dispersion of CNTs in the UHMWPE matrix. Thereby, the crystallization rate of UHMWPE phase in UHMWPE

  18. INVESTIGATION ON THE PHASE INVERSION BEHAVIOR OF WATERBORNE POLYURETHANE DURING EMULSIFICATION PROCESS%水性聚氨酯乳化过程中相转变的研究

    Institute of Scientific and Technical Information of China (English)

    鹿秀山; 郝广杰; 郭天瑛; 宋谋道; 张邦华

    2001-01-01

    本文合成了单官能团小分子物质封端的脂肪族水性聚氨酯预聚物,通过考察预聚物加水乳化过程中粘度及电导率的变化,研究了其相转变行为.实验结果表明,随着软段分子量升高,体系的相转变点后延;聚酯体系的相转变比聚醚体系的相转变发生得早;[NCO]/[OH]值越接近1,体系的粘度就越高,相转变发生所需的水含量也越高;羧基含量及中和度也会对分散体系的相转变产生影响.通过选择合适的条件,可以实现对乳化过程的优化.%Several aliphatic waterborne polyurethane prepolymers are prepared from isophorone diisocyanate,dimethylolpropanic acid,poly(butylene adipate) (PBA) and polypropylene glyco (PPG).The prepolymers are blocked with 2-methoxyethanol,followed by neutralization pendant carboxyl by triethylamine,then diluted to 50?wt% with methyl ethyl ketone,emulsified by adding deionized water under constant agitation.The principle of emulsification is explained.The aggregated structure of prepolymers in organic solvent is discussed.The prepolymer molecules with ionic groups can form segment microionic lattices.The emulsification process and phase inversion are characterized by using the variation of viscosity and conductivity.The emulsification process includes the dissociation of the segment microionic lattices and the aggregation of the hydrophobic segments.The inversion process can be clearly divided into three regions depending upon the variation of viscosity and conductivity.The experimental results show that several factors can affect the phase inversion heavily,including the molecular weight and type of soft segments,the [NCO]/[OH] ratio,carboxyl content and neutralization degree.With the increasing of the molecular weight of soft segment,the phase inversion delays.In addition,the phase inversion of PBA-based prepolymer occurs earlier than that of PPG-based prepolymer,while their soft

  19. 正辛烷热裂化和催化裂化生成甲烷反应机理%Mechanism of methane formation in thermal and catalytic cracking of n-octane

    Institute of Scientific and Technical Information of China (English)

    李福超; 张久顺; 袁起民

    2014-01-01

    The thermal and catalytic cracking reactions of n-octane were carried out in a temperature range of 550~650℃ with low conversions ( x<15%) in a pulse micro-reactor over quartz and ZRP zeolite. Reaction mechanism of methane formation was analyzed. The results showed that ethylene, propylene and n-butylene were primary products and four paths contributed to methane formation in thermal cracking of n-octane. At 600 ℃, dehydrogenation of terminal C-H bond in the chain attacked by methyl radical led to methane production. Due to higher activation energy of cleavage of terminal C-C bond in octyl radical formed via dehydrogenation of central C-C bond, only methane can form at higher temperature. Protolytic cracking was predominant with relatively remarkable yield of normal paraffin in catalytic cracking of n-octane over ZRP zeolite. Methane was produced by protolytic cracking route as well. By comparison of methane formation between thermal and protolytic cracking, it revealed that methane formed through protolytic cracking below 600℃ while thermal cracking dominated the selectivity of methane at higher reaction temperatures.%采用脉冲微反装置,在反应温度为550~650℃,低转化率(小于15%)下,研究了正辛烷在石英砂和ZRP分子筛上的热裂化和催化裂化反应,分析了甲烷的生成机理。结果表明,正辛烷热裂化时,乙烯、丙烯和正丁烯是初始产物,甲烷由4种反应路径生成。当反应温度为600℃时,甲基自由基攻击碳链端部C-H键生成甲烷。中部C-H键脱氢形成的辛基自由基在端部C-C键断裂的活化能较高,仅在高温下生成甲烷。正辛烷在ZRP分子筛上主要发生质子化裂化反应,正构烷烃占有相当比重,甲烷由质子化裂化步骤生成。热裂化与质子化裂化对甲烷贡献的对比可知,当反应温度低于600℃时,甲烷由质子化裂化反应生成;在高温下,热裂化反应决定甲烷选择性。

  20. 食品包装材料生态化发展下的非石油基降解塑料%Non-Petroleum Based Biodegradable Plastic with the Development of Ecologicalization in Food Packaging Materials

    Institute of Scientific and Technical Information of China (English)

    戴宏民; 戴佩燕

    2015-01-01

    -toxic, non-irritating, high strength, easy process-ing and good biocompatibility. Polylactic acid is a kind of biodegradable plastic which could truly realize the dual benefits in ecology and economy with the fastest development. The biodegradable plastic comprehensive properties of butylene succinate are excellent with reasonable cost performance, so it has good application prospect in the fields of food packaging, disposable tableware, packing bottle for medicine, biomedical polymer materials, and auto parts etc. As the packing material, non-petroleum based biodegradable plastic is the inevitable trend with the focus in improving the modified technology and cost control, ensuring non-toxic and harmless to human body, emphasizing individuality, and paying attention to improving the market adoption.

  1. Development of Modified Pag (Polyalkylene Glycol) High VI High Fuel Efficient Lubricant for LDV Applications

    Energy Technology Data Exchange (ETDEWEB)

    Gangopadhyay, Arup [Ford Motor Company, Dearborn, MI (United States); McWatt, D. G. [Ford Motor Company, Dearborn, MI (United States); Zdrodowski, R. J. [Ford Motor Company, Dearborn, MI (United States); Liu, Zak [Ford Motor Company, Dearborn, MI (United States); Elie, Larry [Ford Motor Company, Dearborn, MI (United States); Simko, S. J. [Ford Motor Company, Dearborn, MI (United States); Erdemir, Ali [Argonne National Lab. (ANL), Argonne, IL (United States); Ramirez, Giovanni [Argonne National Lab. (ANL), Argonne, IL (United States); Cuthbert, J. [Dow Chemical Company, Midland, MI (United States); Hock, E. D. [Dow Chemical Company, Midland, MI (United States)

    2015-09-30

    Test Procedure) metro/highway cycles. Five different PAG chemistries were selected by varying the starting alcohol, the oxide monomers (ethylene oxide, propylene oxide, or butylene oxide), capped or uncapped, homopolymer or random copolymer. All formulations contained a proprietary additive package and one which contained additional antiwear and friction modifier additives. Laboratory bench tests (Pin-on-Disk, High Frequency Reciprocating Rig (HFRR), Block-on-Ring, Mini-Traction Machine (MTM) identified formulations having friction, wear, and load carrying characteristics similar to or better than baseline GF-5 SAE 5W-20 oil. Motored valvetrain and motored piston ring friction tests showed nearly 50% friction reduction for some of the PAG formulations compared to GF-5 SAE 5W-20 oil. Motored engine tests showed up to 15% friction benefit over GF-5 SAE 5W-20 oil. It was observed that friction benefits are more related to PAG base oil chemistry than their lower viscosity compared to GF-5 SAE 5W-20 oil. Analysis of wear surfaces from laboratory bench tests and bucket tappets from motored valvetrain tests confirmed the presence of PAG molecules. The adsorption of these polar molecules is believed to be reason for friction reduction. However, the wear surfaces also had thin tribo-film derived from additive components. The tribo-film consisting of phosphates, sulfides, and molybdenum disulfide (when molybdenum additive was present) were observed for both GF-5 SAE 5W-20 and PAG fluids. However, when using PAG fluids, motored valvetrain tests showed high initial wear, which is believed to be due to delay in protective tribo-film formation. After the initial wear, the wear rate of PAG fluids was comparable to GF-5 SAE 5W-20 oil. The PAG oil containing additional antiwear and friction reducing additives showed low initial wear as expected. However, when this oil was evaluated in Sequence IVA test, it showed initially low wear comparable to GF-5 oil but wear accelerated with oil

  2. Viabilidade celular de nanofibras de polímeros biodegradáveis e seus nanocompósitos com argila montmorilonita Cell viability of nanofibers from biodegradable polymers and their nanocomposites with montmorillonite

    Directory of Open Access Journals (Sweden)

    Alfredo M. Goes

    2012-01-01

    Full Text Available Mantas não tecidas de nanofibras de três polímeros biodegradáveis poli(ácido láctico, PDLLA, poli(Ε-caprolactona, PCL, e poli(butileno adipato-co-tereftalato, PBAT e seus nanocompósitos com uma nanoargila montmorilonita (MMT foram produzidas por eletrofiação. A morfologia, o comportamento térmico e a estrutura interna das nanofibras foram analisados por microscopia eletrônica de varredura e transmissão, calorimetria diferencial de varredura e difração de raios X, respectivamente. Observou-se que as nanofibras dos nanocompósitos possuíam diâmetros menores do que os correspondentes polímeros puros e que as nanofibras de PBAT puro e de PBAT/MMT apresentavam a menor cristalinidade de todas as mantas. A viabilidade celular de todas as nanofibras foi analisada pela técnica de redução do sal de tetrazolium pelo complexo enzimático piruvato desidrogenase presente na matriz de mitocôndrias (teste MTT. Os resultados mostraram que nenhuma manta nanofibrílica apresentou toxicidade às células e que as nanofibras de PBAT puro e seu nanocompósito propiciaram ainda um ambiente mais favorável ao desenvolvimento celular de fibroblastos de cardiomiócitos do que as condições oferecidas pelo controles, provavelmente por apresentarem menores diâmetros e baixa cristalinidade em relação às demais nanofibras. Estes resultados mostram o potencial de uso destas mantas nanofibrílicas como suportes de crescimento celular.Non-woven mats of nanofibers of three biodegradable polymers, viz. poly(lactic acid, PDLLA, poly(Ε-caprolactone, PCL, and poly(butylene adipate-co-terephthalate, PBAT, and their nanocomposites with montmorillonite nanoclay (MMT were produced by electrospinning. The morphology, thermal behavior and internal structure of the nanofibers were analyzed by scanning and transmission electron microscopy, differential scanning calorimetry and wide angle X-ray diffraction, respectively. The nanofibers of the nanocomposites had

  3. 含氟丙烯酸酯乳液整理剂的合成及其在织物防水防油整理中的应用%Synthesis of fluoridated acrylic emulsion finishing agent and application in water and oil proofing finish on cotton fabric

    Institute of Scientific and Technical Information of China (English)

    何彦萱; 刘金华; 郭玉良; 刘军; 卢霜

    2014-01-01

    以甲基丙烯酸甲酯、丙烯酸异冰片酯、甲基丙烯酸十二烷基酯、六氟丙烯酸丁酯、二甲基丙烯酸丁二醇酯、3-氯-2-羟丙基甲基丙烯酸酯为单体,偶氮二异丁基脒盐酸盐为引发剂,合成阳离子含氟丙烯酸酯乳液,并应用于棉织物的拒水拒油整理.用红外光谱对聚合物进行表征,研究了交联剂对胶膜接触角及整理棉织物拒水拒油性能的影响.结果表明:未加交联剂,胶膜接触角达111.58°;加2%的三官能团氮丙啶交联剂,胶膜接触角可以提高到118.35°.经该乳液整理后的织物不仅具有较好的拒水性能,而且有突出的拒油性能,拒水达100分,拒油达6级;同时,耐久性良好,水洗30次以后,拒水为90分,拒油为5级.%Cationic fluorinated acrylic emulsions were synthesized with methyl methacrylate, isobornyl ac⁃rylate, lauryl methacrylate, hexafluorobutyl acrylate, butylene glycol dimethacrylate, 3- chloro- 2- hydroxypropyl methacrylate as monomers and azobis isobutyl amidine hydrochloride as the initiator, which was applied in wa⁃ter and oil repel ent finishing of cotton fabrics. The polymer emulsion properties were characterized with infra⁃red spectrometer. The effects of the crosslinking agent on the contact angle of the film and the water and oil repel ent properties of the finished fabrics were investigated. The results showed that the contact angle of the film was 111.58°, when 2% tri- functional aziridine crosslinking agent was added, the contact angle of the film was increased to 118.35°. The results showed that the finished fabric not only had good water repel ence but also had outstanding oil repel ence. The waterproofing level was 100 points, the oil repel ent level was grade 6; at the same time, the durability was excellent, after 30 times of washing, the waterproofing level was 90 points, and the oil repel ent level was grade 5.

  4. SYNTHESIS AND CRYTALLIZATION PROPERTIES OF CATIONIC DYEABLE POLY ( TRIMETHYLENE TEREPHTHALATE) COPOLYESTERS%阳离子染料可染聚对苯二甲酸丙二酯共聚酯的合成及结晶性能的研究

    Institute of Scientific and Technical Information of China (English)

    姚玉元; 江长明; 吕汪洋; 刘恒山; 王秀华; 陈文兴

    2011-01-01

    通过直接酯化-缩聚工艺,在聚对苯二甲酸丙二酯(PTT)聚合的酯化过程中加入第三组分间苯二甲酸丙二酯-5-磺酸钠(SIPP),在缩聚过程中加入第四组分聚1,6-己二酸-1,4-丁二醇酯(PBA)或聚乙二醇(PEG)合成了一系列不同的阳离子染料可染PTT,采用氢核磁共振波谱(1H-NMR)、差示扫描量热仪(DSC)和热重分析(TG)表征了产物的结构和性能.与常规PTT相比,经SIPP、PBA或PEG改性后的阳离子染料可染PTT热降解性能影响不大.利用差示扫描量热仪(DSC)进一步研究了PTT及改性后阳离子染料可染PTT的非等温结晶性能,结果表明PTT的Avrami指数n在4.24~4.50之间,表明PTT的非等温结晶成核受均相成核和异相成核的双重影响,结晶比较复杂;PTT经SIPP、PBA和PEG改性后的Avrami指数n在1.72~2.64之间,推测它的成核机理主要是异相成核,并且结晶活化能高于常规PTT,说明阳离子染料可染PTT的结晶对温度比较敏感,因此在纺丝过程中控制温度至关重要.%The third component of 5-sulfoisophthalic acid dihydroxy propyl ester sodium salt (SIPP) and the fourth component of poly( butylene adipate) (PBA) or polyethylene glycol (PEG) were added respectively in the process of esterification and polycondensation for the polymerization of 1,3-propanediol ( or trimethylene glycol) and terephthalic acid. Three kinds of cationic dyeable poly (trimethylene terephtalate) copolyesters (PTTs) were synthesized by direct esterification-polycondensation process, and were characterized by differential scanning calorimetry ( DSC ),1 H-nuclear magnetic resonance ( 1 H-NMR ) and thermogravimetric analysis (TGA), respectively. Compared to PTT, the thermal degrodation properties for PTTs modified by SIPP, PBA and PEG almost kept invariant. DSC was used to further investigate the nonisothermal crystallization properties of PTT and the cationic dyeable PTTs, and the experimental results indicated that the Avrami

  5. Preparation and characterization of biodegradable polymer-coated urea%可生物降解树脂包膜尿素的研制及性能

    Institute of Scientific and Technical Information of China (English)

    王州; 张坤; 徐静; 张民

    2013-01-01

    Two kinds of biodegradable polymers, poly(propylene carbonate)(PPC) and poly(butylenes succinate) ( PBS) , were used as slow-released film for urea , and ratios of PPC/PBS in solution are adjusted in range of 12∶0-0∶12.After evaporating the solvent , the PPC/PBS membranes were obtained in various ratios .The PPC/PBS-coated slow-released urea was prepared by spouted-spraying method , nitrogen release was investigated by Ultraviolet Spectrophotometry method , and scanning electronic microscopy ( SEM ) was used to observe the structure of the coating film.The results show that the flexible and compatible membrane is the best under the ratio of 7∶5.When the weight ratio of PPC∶PBS is about 7∶5 , the composite material possesses strong film characteristic , comparable and flexible .The PPC/PBS film is found suitable to the rugged surface of urea and combined tightly with the surface of urea .The PPC/PBS coated urea shows remarkable controlling function of urea nitrogen release .These results also prove that reducing envelope time or increasing resin quality can enhance the quality of controlled release effect .%以聚碳酸亚丙酯( PPC)与聚丁二酸丁二醇酯( PBS)两种可生物降解树脂作为包膜材料,研制不同PPC/PBS组方包膜溶液,铺膜后初步确定两种材料混合的最佳比例;采用流化喷涂分别制备包膜尿素。通过分光光度法研究不同肥料的初期溶出率,采用扫描电镜观察包膜结构。结果表明,PPC与PBS的质量比在7∶5时,材料之间融合较好,质地较柔软,适合作为肥料包膜材料。实验证明此包膜材料在尿素表面能够形成细腻光滑致密的膜,可以适应尿素颗粒表面的外形轮廓而将其紧密覆盖。尿素包膜后,对尿素氮的释放有明显的控释作用,且在一定范围内,减少包膜所用时间或增加树脂用量都能增强控释效果。

  6. Preparation of Porous Composite Membrane Based on Surface Grafting of Modified Chitosan by Waterborne Polyurethane%多孔水性聚氨酯表面接枝改性硫酸化壳聚糖复合膜的制备

    Institute of Scientific and Technical Information of China (English)

    王晓静; 李国明; 刘聪; 谢胜; 董玉雪

    2015-01-01

    Waterborne polyurethane was synthesized by the reaction of HDI trimmers (HT),toluene diisocyanate (TDI) and polyethylene glycol(PEG800) as raw materials,1,4-butylene glycol(BDO),2,2-dimethylol propionic acid( DMPA) and ethylenediamine( EDA) as hydrophilic chain extender.CaCO3 was used as pore-foaming agent to prepare the WPU porous composite membrane.Then,the WPU/SCS porous composite membrane was generated by surface grafting of sulfated chitosan onto the WPU porous composite membrane.The effects of the contents of pore-foaming agent on the porosity and water absorption of WPU/SCS porous composite membrane have been studied. The structure of the composite membrane was studied by Fourier transformation infrared spectrometer( FTIR) ,and the morphologies of the composite membrane were characterized by optical polarization micrograph ( OPM ) .The recalification time test and dynamic blood-clotting test were used to characterize the blood compatibility of the com-posite membrane.The results showed that the porosity and water absorption of the composite membrane were 68.3%and 112.5%respectively when the content of CaCO3 was 12%,the composite membrane possesed excellent blood compatibility.It was expected to be an excellent biomedical material.%采用己二异氰酸酯三聚体( HT)、2,4-甲苯二异氰酸酯( TDI)、聚乙二醇800为基本原料,以1,4-丁二醇、2,2-二甲基丙酸和乙二胺为亲水扩链剂,合成了水性聚氨酯( WPU),以CaCO3作为致孔剂制备多孔WPU膜,并与硫酸化壳聚糖( SCS)接枝,制得多孔WPU/SCS复合膜,探讨了致孔剂的用量对WPU/SCS复合膜孔隙率和吸水率的影响.利用红外光谱仪和光学显微镜对复合膜的结构和形态进行了表征,并通过复钙化时间和动态凝血时间对其血液相容性进行了表征.结果表明,致孔剂CaCO3使用量为12%时,孔隙率为68.3%,吸水率达112.5%,多孔WPU/SCS复合膜具有较好的

  7. Design of biobased and biodegradable - compostable engineered plastics based on poly(lactide)

    Science.gov (United States)

    Schneider, Jeffrey Samuelson

    Poly(lactide) (PLA) is a biobased and biodegradable - compostable plastic that is derived from renewable resources such as corn and sugar cane. It possesses excellent strength and stiffness properties and is recognized as safe for biomedical and food packaging applications. Commercially, it costs $1/lb and is now competitive with petroleum based polymers that have dominated the industry for decades. However, the material has some inherently weak properties that prevent it from certain applications - most notably, its rheological properties, brittleness, and poor high temperature performance. Cost effective modifications of the polymer to enhance these deficiencies could allow for increased applications and further its commercial growth. Multiple synthetic strategies have been developed to address PLA's performance property deficiencies. PLA typically exhibits poor melt strength and does not have the ability to strain harden, partially a result of its highly linear nature. Strain hardening and high melt strength are crucial elements of a material when producing blown films, a large untapped market for PLA. By increasing molecular weight and introducing long-chain branching into the material, these properties can be improved. Epoxy-functionalized PLA (EF-PLA) was synthesized by reacting PLA with a multifunctional epoxy polymer (MEP) using reactive extrusion processing (REX). These modified PLA polymers can function as a rheology modifier for PLA and a compatibilizer for blends with other biopolyesters. The modified PLA showed an increased melt strength and exhibited significant strain hardening, thus making it more suited for blown film applications. Blown films comprised of PLA and poly(butylene adipate-co-terephthalate) (PBAT) were produced using EF-PLA as a reactive modifier for rheological enhancement and compatibilization. This resulted in films with better processability (as seen by increased bubble stability) and improved mechanical properties, compared to a

  8. 催化干气制乙苯和高辛烷值汽油组分技术开发与应用%Development and application of producing technology for ethylbenzene and high-octane rating gasoline component from FCC dry gas

    Institute of Scientific and Technical Information of China (English)

    刘文杰; 杨为民

    2015-01-01

    Aiming to fully utilize the dilute ethylene of FCC off gas of the refinery,the process technology for ethylbenzene production from dilute ethylene was developed. The technique used the pre-treatment process to remove propylene and butylenes from raw dry gas,and SEB series catalysts for the vapor phase alkylation of benzene with dilute ethylene. Under the condition of reaction temperature(320 - 380)℃,reaction pressure(0. 7 - 1. 0)MPa,benzene / ethylene molar ratio 5. 0 - 7. 0,ethylene conversion was more than 99% . For production of 1 ton ethylbenzene,the consumption of benzene and ethylene in FCC off-gas,and the energy consumption were 0. 75 t,0. 275 t and 150 kilograms of standard oil,respectively. The purity of ethylbenzene was over 99. 8% and the content of main impurity xylene in the product was < 0. 08% . This process technology had been applied successfully in 9 plants. Because the octane rating in the blended gasoline was insufficient,the process for dilute ethylene to produce ethylbenzene was optimized,in which the pre-treatment unit of removing propylene was omitted and other distillation units following benzene column were cut,and therefore benzene / ethylene molar ratio could be reduced to 4. 0 - 5. 0. Energy consumption of per ton product was reduced to about 80 kilograms of standard oil,and the octane rating of the obtained blended gasoline was up to 108. 1,which met the requirement of octane rating of the blended gasoline. The resource of dilute ethylene was effectively utilized. The two techniques could help the comprise to flexibly produce ethylbenzene or high-octane rating gasoline component according to the market and plant’s operation situation.%为充分利用炼油厂干气中的稀乙烯资源,设计开发了稀乙烯制乙苯成套技术(SGEB)。该技术采用预处理工艺脱除原料干气中的丙烯和丁烯,苯和乙烯气相烷基化反应部分使用高效 SEB系列稀乙烯制乙苯催化剂,在反应温度(320~380

  9. Spectroelectrochemical Sensor for Pertechnetate Applicable to Hanford and Other DOE Sites

    Energy Technology Data Exchange (ETDEWEB)

    Heineman, William R; Seliskar, Carl J; Bryan, Samuel A

    2012-09-18

    The general aim of our work funded by DOE is the design and implementation of a new sensor technology that offers unprecedented levels of specificity needed for analysis of the complex chemical mixtures found at DOE sites nationwide. The specific goal of this project was the development of a sensor for technetium (Tc) that is applicable to characterizing and monitoring the vadose zone and associated subsurface water at the Hanford Site and other DOE sites. The concept for the spectroelectrochemical sensor is innovative and represents a breakthrough in sensor technology. The sensor combines three modes of selectivity (electrochemistry, spectroscopy, and selective partitioning) into a single sensor to substantially improve selectivity. The sensor consists of a basic spectroelectrochemical configuration that we have developed under our previous DOE grants: a waveguide with an optically transparent electrode (OTE) that is coated with a thin chemically-selective film that preconcnetrates the analyte. The key to adapting this generic sensor to detect TcO4- and Tc complexes lies in the development of chemically-selective films that preconcentrate the analyte and, when necessary, chemically convert it into a complex with electrochemical and spectroscopic properties appropriate for sensing. Significant accomplishments were made in the general areas of synthesis and characterization of polymer films that efficiently preconcentrate the analyte, development and characterization of sensors and associated instrumentation, and synthesis and characterization of relevant Re and Tc complexes. Two new polymer films for the preconcentration step in the sensor were developed: partially sulfonated polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SSEBS) and phosphine containing polymer films. The latter was a directed polymer film synthesis that combined the proper electrostatic properties to attract TcO4- and also incorporated a suitable ligand for covalently trapping a

  10. Development of Modified Pag (Polyalkylene Glycol) High VI High Fuel Efficient Lubricant for LDV Applications

    Energy Technology Data Exchange (ETDEWEB)

    Gangopadhyay, Arup [Ford Motor Company, Dearborn, MI (United States); McWatt, D. G. [Ford Motor Company, Dearborn, MI (United States); Zdrodowski, R. J. [Ford Motor Company, Dearborn, MI (United States); Liu, Zak [Ford Motor Company, Dearborn, MI (United States); Elie, Larry [Ford Motor Company, Dearborn, MI (United States); Simko, S. J. [Ford Motor Company, Dearborn, MI (United States); Erdemir, Ali [Argonne National Lab. (ANL), Argonne, IL (United States); Ramirez, Giovanni [Argonne National Lab. (ANL), Argonne, IL (United States); Cuthbert, J. [Dow Chemical Company, Midland, MI (United States); Hock, E. D. [Dow Chemical Company, Midland, MI (United States)

    2015-09-30

    Test Procedure) metro/highway cycles. Five different PAG chemistries were selected by varying the starting alcohol, the oxide monomers (ethylene oxide, propylene oxide, or butylene oxide), capped or uncapped, homopolymer or random copolymer. All formulations contained a proprietary additive package and one which contained additional antiwear and friction modifier additives. Laboratory bench tests (Pin-on-Disk, High Frequency Reciprocating Rig (HFRR), Block-on-Ring, Mini-Traction Machine (MTM) identified formulations having friction, wear, and load carrying characteristics similar to or better than baseline GF-5 SAE 5W-20 oil. Motored valvetrain and motored piston ring friction tests showed nearly 50% friction reduction for some of the PAG formulations compared to GF-5 SAE 5W-20 oil. Motored engine tests showed up to 15% friction benefit over GF-5 SAE 5W-20 oil. It was observed that friction benefits are more related to PAG base oil chemistry than their lower viscosity compared to GF-5 SAE 5W-20 oil. Analysis of wear surfaces from laboratory bench tests and bucket tappets from motored valvetrain tests confirmed the presence of PAG molecules. The adsorption of these polar molecules is believed to be reason for friction reduction. However, the wear surfaces also had thin tribo-film derived from additive components. The tribo-film consisting of phosphates, sulfides, and molybdenum disulfide (when molybdenum additive was present) were observed for both GF-5 SAE 5W-20 and PAG fluids. However, when using PAG fluids, motored valvetrain tests showed high initial wear, which is believed to be due to delay in protective tribo-film formation. After the initial wear, the wear rate of PAG fluids was comparable to GF-5 SAE 5W-20 oil. The PAG oil containing additional antiwear and friction reducing additives showed low initial wear as expected. However, when this oil was evaluated in Sequence IVA test, it showed initially low wear comparable to GF-5 oil but wear accelerated with oil

  11. Phenolic resin-based porous carbons for adsorption and energy storage applications

    Science.gov (United States)

    Wickramaratne, Nilantha P.

    view. So far, carbons with high surface area and nitrogen content have been vastly studied. Also, there are several reports showing the importance of pore size towards CO2 adsorption at ambient conditions. In the case of nitrogen containing carbons, it was shown that the incorporation of nitrogen into carbon matrix is a challenging task. In chapter 3, we discussed how to improve the surface area and pore size distribution of phenolic resin-based carbons to obtain optimum CO 2 adsorption capacities at ambient conditions. The chemical and physical activation of polymer/carbon particles is used to generate necessary physical properties of the final carbons, which display unprecedented CO2 adsorption capacities at ambient conditions. Moreover, the modified Stober-like methods are used for the synthesis of nitrogen containing carbon particles. These facile synthesis methods afford highly porous nitrogen containing carbons with comparatively high CO2 adsorption capacities at ambient conditions. Chapter 4 begins with synthesis of ultra large mesoporous carbons using (ethylene oxide)38 (butylene oxide)46 (ethylene oxide) 38 triblock copolymer as a soft template and phenolic resins as the carbon precursors. Even though, there are many reports dealing with the synthesis of mesoporous silica with large pores for bio-molucular adsorption their high cost discourage them to use in industrial applications. However, cheap mesoporous carbons with large pores (>15 nm) are potential materials for bio-molecular adsorption on large scale. The first part of chapter 4 is demonstrates the synthesis of mesoporous carbons with ultra large pores for bio-molecular adsorption. Lysozyme was selected as a model biomolecule for adsorption processes. The second part of Chapter 4 is focused on functionalized polymer spheres for heavy metal ions adsorption. It is shown that the synthesis of functionalized polymer spheres can be achieved by using modified Stober method; the reacting spheres show very

  12. Spectroelectrochemical Sensor for Pertechnetate Applicable to Hanford and Other DOE Sites

    Energy Technology Data Exchange (ETDEWEB)

    Heineman, William R; Seliskar, Carl J; Bryan, Samuel A

    2012-09-18

    The general aim of our work funded by DOE is the design and implementation of a new sensor technology that offers unprecedented levels of specificity needed for analysis of the complex chemical mixtures found at DOE sites nationwide. The specific goal of this project was the development of a sensor for technetium (Tc) that is applicable to characterizing and monitoring the vadose zone and associated subsurface water at the Hanford Site and other DOE sites. The concept for the spectroelectrochemical sensor is innovative and represents a breakthrough in sensor technology. The sensor combines three modes of selectivity (electrochemistry, spectroscopy, and selective partitioning) into a single sensor to substantially improve selectivity. The sensor consists of a basic spectroelectrochemical configuration that we have developed under our previous DOE grants: a waveguide with an optically transparent electrode (OTE) that is coated with a thin chemically-selective film that preconcnetrates the analyte. The key to adapting this generic sensor to detect TcO4- and Tc complexes lies in the development of chemically-selective films that preconcentrate the analyte and, when necessary, chemically convert it into a complex with electrochemical and spectroscopic properties appropriate for sensing. Significant accomplishments were made in the general areas of synthesis and characterization of polymer films that efficiently preconcentrate the analyte, development and characterization of sensors and associated instrumentation, and synthesis and characterization of relevant Re and Tc complexes. Two new polymer films for the preconcentration step in the sensor were developed: partially sulfonated polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SSEBS) and phosphine containing polymer films. The latter was a directed polymer film synthesis that combined the proper electrostatic properties to attract TcO4- and also incorporated a suitable ligand for covalently trapping a