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Sample records for crystal polyester monomers

  1. Liquid crystal polyester thermosets

    Science.gov (United States)

    Benicewicz, Brian C.; Hoyt, Andrea E.

    1992-01-01

    The present invention provides (1) curable liquid crystalline polyester monomers represented by the formula: R.sup.1 --A.sup.1 --B.sup.1 --A.sup.2 --B.sup.2 --A.sup.3 --R.sup.2 where R.sup.1 and R.sup.2 are radicals selected from the group consisting of maleimide, substituted maleimide, nadimide, substituted naimide, ethynyl, and (C(R.sup.3).sub.2).sub.2 where R.sup.3 is hydrogen with the proviso that the two carbon atoms of (C(R.sup.3).sub.2).sub.2 are bound on the aromatic ring of A.sup.1 or A.sup.3 to adjacent carbon atoms, A.sup.1 and A.sup.3 are 1,4-phenylene and the same where said group contains one or more substituents selected from the group consisting of halo, e.g., fluoro, chloro, bromo, or iodo, nitro lower alkyl, e.g., methyl, ethyl, or propyl, alkoxy, e.g., methoxy, ethoxy, or propoxy, and fluoroalkyl, e.g., trifluoromethyl, pentafluoroethyl and the like, A.sup.2 is selected from the group consisting of 1,4-phenylene, 4,4'-biphenyl, 2,6-naphthylene and the same where said groups contain one or more substituents selected from the group consisting of halo, e.g., fluoro, chloro, bromo, or iodo, nitro, lower alkyl, e.g., methyl, ethyl, and propyl, lower alkoxy, e.g., methoxy, ethoxy, or propoxy, and fluoroalkyl or fluoroalkoxy, e.g., trifluoromethyl, pentafluoroethyl and the like, and B.sup.1 and B.sup.2 are selected from the group consisting of --C(O)--O-- and --O--C(O)--, (2) thermoset liquid crystalline polyester compositions comprised of heat-cured segments derived from monomers represented by the formula: R.sup.1 --A.sup.1 --B.sup.1 --A.sup.2 --B.sup.2 --A.sup.3 --R.sup.2 as described above, (3) curable blends of at least two of the polyester monomers and (4) processes of preparing the curable liquid crystalline polyester monomers.

  2. Design and Applications of Biodegradable Polyester Tissue Scaffolds Based on Endogenous Monomers Found in Human Metabolism

    Directory of Open Access Journals (Sweden)

    Devin G. Barrett

    2009-10-01

    Full Text Available Synthetic polyesters have deeply impacted various biomedical and engineering fields, such as tissue scaffolding and therapeutic delivery. Currently, many applications involving polyesters are being explored with polymers derived from monomers that are endogenous to the human metabolism. Examples of these monomers include glycerol, xylitol, sorbitol, and lactic, sebacic, citric, succinic, α-ketoglutaric, and fumaric acids. In terms of mechanical versatility, crystallinity, hydrophobicity, and biocompatibility, polyesters synthesized partially or completely from these monomers can display a wide range of properties. The flexibility in these macromolecular properties allows for materials to be tailored according to the needs of a particular application. Along with the presence of natural monomers that allows for a high probability of biocompatibility, there is also an added benefit that this class of polyesters is more environmentally friendly than many other materials used in biomedical engineering. While the selection of monomers may be limited by nature, these polymers have produced or have the potential to produce an enormous number of successes in vitro and in vivo.

  3. Facile synthesis of polyester dendrimers from sequential click coupling of asymmetrical monomers.

    Science.gov (United States)

    Ma, Xinpeng; Tang, Jianbin; Shen, Youqing; Fan, Maohong; Tang, Huadong; Radosz, Maciej

    2009-10-21

    Polyester dendrimers are attractive for in vivo delivery of bioactive molecules due to their biodegradability, but their synthesis generally requires multistep reactions with intensive purifications. A highly efficient approach to the synthesis of dendrimers by simply "sticking" generation by generation together is achieved by combining kinetic or mechanistic chemoselectivity with click reactions between the monomers. In each generation, the targeted molecules are the major reaction product as detected by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS). The only separation needed is to remove the little unreacted monomer by simple precipitation or washing. This simple clicklike process without complicated purification is particularly suitable for the synthesis of custom-made polyester dendrimers.

  4. Qualitative and quantitative analysis of monomers in polyesters for food contact materials.

    Science.gov (United States)

    Brenz, Fabrian; Linke, Susanne; Simat, Thomas

    2017-02-01

    Polyesters (PESs) are gaining more importance on the food contact material (FCM) market and the variety of properties and applications is expected to be wide. In order to acquire the desired properties manufacturers can combine several FCM-approved polyvalent carboxylic acids (PCAs) and polyols as monomers. However, information about the qualitative and quantitative composition of FCM articles is often limited. The method presented here describes the analysis of PESs with the identification and quantification of 25 PES monomers (10 PCA, 15 polyols) by HPLC with diode array detection (HPLC-DAD) and GC-MS after alkaline hydrolysis. Accurate identification and quantification were demonstrated by the analysis of seven different FCM articles made of PESs. The results explained between 97.2% and 103.4% w/w of the polymer composition whilst showing equal molar amounts of PCA and polyols. Quantification proved to be precise and sensitive with coefficients of variation (CVs) below 6.0% for PES samples with monomer concentrations typically ranging from 0.02% to 75% w/w. The analysis of 15 PES samples for the FCM market revealed the presence of five different PCAs and 11 different polyols (main monomers, co-monomers, non-intentionally added substances (NIAS)) showing the wide variety of monomers in modern PESs. The presented method provides a useful tool for commercial, state and research laboratories as well as for producers and distributors facing the task of FCM risk assessment. It can be applied for the identification and quantification of migrating monomers and the prediction of oligomer compositions from the identified monomers, respectively.

  5. Synthesis of poly(ethylene furandicarboxylate) polyester using monomers derived from renewable resources: thermal behavior comparison with PET and PEN.

    Science.gov (United States)

    Papageorgiou, George Z; Tsanaktsis, Vasilios; Bikiaris, Dimitrios N

    2014-05-07

    Poly(ethylene-2,5-furandicarboxylate) (PEF) is a new alipharomatic polyester that can be prepared from monomers derived from renewable resources like furfural and hydroxymethylfurfural. For this reason it has gained high interest recently. In the present work it was synthesized from the dimethylester of 2,5-furandicarboxylic acid and ethylene glycol by applying the two-stage melt polycondensation method. The thermal behavior of PEF was studied in comparison to its terephthalate and naphthalate homologues poly(ethylene terephthalate) (PET) and poly(ethylene naphthalate) (PEN), which were also synthesized following the same procedure. The equilibrium melting point of PEF was found to be 265 °C while the heat of fusion for the pure crystalline PEF was estimated to be about 137 J g(-1). The crystallization kinetics was analyzed using various models. PET showed faster crystallization rates than PEN and this in turn showed faster crystallization than PEF, under both isothermal and non-isothermal conditions. The spherulitic morphology of PEF during isothermal crystallization was investigated by polarized light microscopy (PLM). A large nucleation density and a small spherulite size were observed for PEF even at low supercoolings, in contrast to PET or PEN. Thermogravimetric analysis indicated that PEF is thermally stable up to 325 °C and the temperature for the maximum degradation rate was 438 °C. These values were a little lower than those for PET or PEN.

  6. Non-isothermal Crystallization Kinetics of Kaolin Modified Polyester

    Institute of Scientific and Technical Information of China (English)

    ZHANG Ruixin; GU Mingbo; CHEN Guoqiang

    2011-01-01

    Fiber-class modified kaolin and PET have been blended in the twin-screw and granulated to chips containing 4 wt% of kaolin.Non-isothermal crystallization process of kaolin modified polyester was investigated using a differential scanning calorimetry (DSC),and the addition of kaolin enhances either the melting temperature (Tm) or the crystallization temperature (Tc).The morphology of kaolin modified polyester,the melt of which is cooled at different cooling rate,was observed by scanning electron microscope (SEM).The relationship between Tc and cooling rate F was studied.Semi-crystalline phase t1/2 makes an exponential decline with increasing F,and the higher the cooling rate,the shorter the time of crystallization completion.Non-isothermal crystallization kinetics parameters and the activation energy were calculated,indicating that the higher rate of cooling needs the higher relative crystallinity in the unit crystallization time,the crystallization rate increased while speeding up the temperature reduction,and the activation energy AE was calculated to be -204.1566 kJ/mol for the non-isothermal crystallization processes by the Kissinger's methods.

  7. Environmentally benign synthesis of saturated and unsaturated aliphatic polyesters via enzymatic polymerization of biobased monomers derived from renewable resources

    NARCIS (Netherlands)

    Jiang, Yi; Woortman, Albert J. J.; van Ekenstein, Gert O. R. Alberda; Loos, Katja

    2015-01-01

    Aliphatic polyesters are of great interest due to their broad potential applications and sustainability. Itaconate-based aliphatic polyesters are even more appealing in biomedical and pharmaceutical fields, as they are renewable functional polymers that can be biodegradable, biocompatible, and

  8. Enzyme-catalyzed synthesis of unsaturated aliphatic polyesters based on green monomers from renewable resources.

    Science.gov (United States)

    Jiang, Yi; Woortman, Albert J J; van Ekenstein, Gert O R Alberda; Loos, Katja

    2013-08-12

    Bio-based commercially available succinate, itaconate and 1,4-butanediol are enzymatically co-polymerized in solution via a two-stage method, using Candida antarctica Lipase B (CALB, in immobilized form as Novozyme® 435) as the biocatalyst. The chemical structures of the obtained products, poly(butylene succinate) (PBS) and poly(butylene succinate-co-itaconate) (PBSI), are confirmed by 1H- and 13C-NMR. The effects of the reaction conditions on the CALB-catalyzed synthesis of PBSI are fully investigated, and the optimal polymerization conditions are obtained. With the established method, PBSI with tunable compositions and satisfying reaction yields is produced. The 1H-NMR results confirm that carbon-carbon double bonds are well preserved in PBSI. The differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA) results indicate that the amount of itaconate in the co-polyesters has no obvious effects on the glass-transition temperature and the thermal stability of PBS and PBSI, but has significant effects on the melting temperature.

  9. Enzyme-Catalyzed Synthesis of Unsaturated Aliphatic Polyesters Based on Green Monomers from Renewable Resources

    Directory of Open Access Journals (Sweden)

    Yi Jiang

    2013-08-01

    Full Text Available Bio-based commercially available succinate, itaconate and 1,4-butanediol are enzymatically co-polymerized in solution via a two-stage method, using Candida antarctica Lipase B (CALB, in immobilized form as Novozyme® 435 as the biocatalyst. The chemical structures of the obtained products, poly(butylene succinate (PBS and poly(butylene succinate-co-itaconate (PBSI, are confirmed by 1H- and 13C-NMR. The effects of the reaction conditions on the CALB-catalyzed synthesis of PBSI are fully investigated, and the optimal polymerization conditions are obtained. With the established method, PBSI with tunable compositions and satisfying reaction yields is produced. The 1H-NMR results confirm that carbon-carbon double bonds are well preserved in PBSI. The differential scanning calorimetry (DSC and thermal gravimetric analysis (TGA results indicate that the amount of itaconate in the co-polyesters has no obvious effects on the glass-transition temperature and the thermal stability of PBS and PBSI, but has significant effects on the melting temperature.

  10. Environmentally benign synthesis of saturated and unsaturated aliphatic polyesters via enzymatic polymerization of biobased monomers derived from renewable resources

    NARCIS (Netherlands)

    Jiang, Yi; Woortman, Albert J. J.; van Ekenstein, Gert O. R. Alberda; Loos, Katja

    2015-01-01

    Aliphatic polyesters are of great interest due to their broad potential applications and sustainability. Itaconate-based aliphatic polyesters are even more appealing in biomedical and pharmaceutical fields, as they are renewable functional polymers that can be biodegradable, biocompatible, and photo

  11. Proton-Transfer Polymerization by N-Heterocyclic Carbenes: Monomer and Catalyst Scopes and Mechanism for Converting Dimethacrylates into Unsaturated Polyesters

    KAUST Repository

    Hong, Miao

    2016-01-18

    This contribution presents a full account of experimental and theoretical/computational investigations into the N-heterocyclic carbene (NHC)-catalyzed proton-transfer polymerization (HTP) that converts common dimethacrylates (DMAs) containing no protic groups into unsaturated polyesters. This new HTP proceeds through the step-growth propagation cycles via enamine intermediates, consisting of the proposed conjugate addition–proton transfer–NHC release fundamental steps. This study examines the monomer and catalyst scopes as well as the fundamental steps involved in the overall HTP mechanism. DMAs having six different types of linkages connecting the two methacrylates have been polymerized into the corresponding unsaturated polyesters. The most intriguing unsaturated polyester of the series is that based on the biomass-derived furfuryl dimethacrylate, which showed a unique self-curing ability Four MeO– and Cl–substituted TPT (1,3,4-triphenyl-4,5-dihydro-1H-1,2,4-triazol-5-ylidene) derivatives as methanol insertion products, RxTPT(MeO/H) (R = MeO, Cl; x = 2, 3), and two free carbenes (catalysts), OMe2TPT and OMe3TPT, have been synthesized, while OMe2TPT(MeO/H) and OMe2TPT have also been structurally characterized. The structure/reactivity relationship study revealed that OMe2TPT, being both a strong nucleophile and a good leaving group, exhibits the highest HTP activity and also produced the polyester with the highest Mn, while the Cl–substituted TPT derivatives are least active and efficient. Computational studies have provided mechanistic insights into the tail-to-tail dimerization coupling step as a suitable model for the propagation cycle of the HTP. The extensive energy profile was mapped out and the experimentally observed unicity of the TPT-based catalysts was satisfactorily explained with the thermodynamic formation of key spirocyclic species.

  12. Enzymatic Polymerization of Cyclic Monomers in Ionic Liquids as a Prospective Synthesis Method for Polyesters Used in Drug Delivery Systems

    Directory of Open Access Journals (Sweden)

    Urszula Piotrowska

    2014-12-01

    Full Text Available Biodegradable or bioresorbable polymers are commonly used in various pharmaceutical fields (e.g., as drug delivery systems, therapeutic systems or macromolecular drug conjugates. Polyesters are an important class of polymers widely utilized in pharmacy due to their biodegradability and biocompatibility features. In recent years, there has been increased interest in enzyme-catalyzed ring-opening polymerization (e-ROP of cyclic esters as an alternative method of preparation of biodegradable or bioresorbable polymers. Ionic liquids (ILs have been presented as green solvents in enzymatic ring-opening polymerization. The activity, stability, selectivity of enzymes in ILs and the ability to catalyze polyester synthesis under these conditions are discussed. Overall, the review demonstrates that e-ROP of lactones or lactides could be an effective method for the synthesis of useful biomedical polymers.

  13. Chemistry of Discotic Liquid Crystals From Monomers to Polymers

    CERN Document Server

    Kumar, Sandeep

    2010-01-01

    Compiling the scattered literature into a single seminal work, this book describes the basic design principles, synthesis, and mesomorphic properties of discotic liquid crystals. Of fundamental importance as models for the study of energy and charge migration in self-organized systems, discotic liquid crystals find functional application as one-dimensional conductors, photoconductors, light emitting diodes, photovoltaic solar cells, field-effect transistors, and gas sensors. This book highlights the scientific concepts behind the hierarchical self-assembly of these disc-shaped molecules alongs

  14. Non-isothermal crystallization kinetics of polypropylene and hyperbranched polyester blends☆

    Institute of Scientific and Technical Information of China (English)

    Qingchun Fan; Feihong Duan; Huaibing Guo; Tian Wu

    2015-01-01

    Polypropylene (PP) with different contents of the second generation hyperbranched polyester (HBP) is prepared by melt blending method. The non-isothermal crystallization kinetics of PP and PP/HBP blends is investigated under differential scanning calorimetry (DSC). The Mo equation is used to analyze the DSC data. The results show that the Mo theory is suitable for crystal ization kinetics of the blends. Fast cooling rate is not good for crys-tallizing and nucleating. The values of half crystal ization time (t1/2), crystal ization enthalpy (ΔHc) and temper-ature range (ΔT) of PP/HBP blends decrease when HBP is added. The required cooling rate of PP is higher than that of PP/HBP blends in order to reach the same relative crystal inity. Crystallization rate increases with the ad-dition of HBP. The crystallization rate reaches a maximum when the content of HBP is 5%. In addition, the activa-tion energies of PP and PP/HBP blends are calculated by Kissinger equation, revealing that the content of HBP has a little effect on the crystallization activation energy.

  15. Molecular alignment enhancement phenomenon of polymer formed from a liquid crystal monomer in a liquid crystal solvent

    Science.gov (United States)

    Fujikake, Hideo; Murashige, Takeshi; Sato, Hiroto; Kawakita, Masahiro; Kikuchi, Hiroshi

    2003-03-01

    We report an abnormal alignment enhancement phenomenon of polymer molecules. The alignment order of a rigid-skeleton polymer made from a liquid crystalline monomer in a low-molecular-weight liquid crystal solvent was drastically enhanced with increasing temperature, even though the alignment order of the solution of the liquid crystal and monomer decreased. From polymer molecular alignment observations using polarizing Raman scattering microscopy, it was found that the polymer alignment order was three times greater than that of the original aligned monomer and polymer. This super alignment technique of polymer using a molecular-scaled self-assembly mechanism is applicable to the formation of electrically and/or optically functional nanopolymer wires.

  16. Close-packed polymer crystals from two-monomer-connected precursors

    Science.gov (United States)

    Lee, Hong-Joon; Jo, Yong-Ryun; Kumar, Santosh; Yoo, Seung Jo; Kim, Jin-Gyu; Kim, Youn-Joong; Kim, Bong-Joong; Lee, Jae-Suk

    2016-09-01

    The design of crystalline polymers is intellectually stimulating and synthetically challenging, especially when the polymerization of any monomer occurs in a linear dimension. Such linear growth often leads to entropically driven chain entanglements and thus is detrimental to attempts to realize the full potential of conjugated molecular structures. Here we report the polymerization of two-monomer-connected precursors (TMCPs) in which two pyrrole units are linked through a connector, yielding highly crystalline polymers. The simultaneous growth of the TMCP results in a close-packed crystal in polypyrrole (PPy) at the molecular scale with either a hexagonal close-packed or face-centred cubic structure, as confirmed by high-voltage electron microscopy, and the structure that formed could be controlled by simply changing the connector. The electrical conductivity of the TMCP-based PPy is almost 35 times that of single-monomer-based PPy, demonstrating its promise for application in diverse fields.

  17. Phase separation of monomer in liquid crystal mixtures and surface morphology in polymer-stabilized vertical alignment liquid crystal displays

    Energy Technology Data Exchange (ETDEWEB)

    Lyu, Jae Jin; Lee, Jun Hyup; Kim, Kyeong Hyeon [Development Center, LCD Business, SAMSUNG Electronics Co. LTD., Tangjeong-Myeon, Asan, Chungnam 336-741 (Korea, Republic of); Kikuchi, Hirotsuku; Higuchi, Hiroki [Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasuga-Koen, Kasuga 816-8580 (Japan); Kim, Dae Hyun; Lee, Seung Hee, E-mail: jsquare.lyu@samsung.com, E-mail: lsh1@chonbuk.ac.kr [Department of BIN Fusion Technology and Department of Polymer-Nano Science and Technology, Chonbuk National University, Jeonju, Jeonbuk 561-756 (Korea, Republic of)

    2011-08-17

    The polymer-stabilized vertically aligned (PS-VA) liquid crystal display (LCD) driving mode has high potential for manufacturing low power consuming displays due to the higher transmittance and fast response as compared with the existing patterned vertically aligned and multi-domain vertically aligned modes. In this paper we have investigated the reaction mechanisms of monomer-liquid crystal blends to form a surface pre-tilt angle of liquid crystal in vertical alignment LCD associated with a fishbone electrode structure. The observed sizes of polymer bumps formed on the substrates were found to be dependent on the exposed UV wavelength and were almost equal in both top and bottom substrates. When a large UV wavelength was used, the phase separation mechanism of monomer in PS-VA mode was found nearly isotropic rather than anisotropic in contrast to the previous studies.

  18. Effect of Molecular Weight on Liquid Crystal Photoalignment by Photosensitive Polyester Containing Thrifluoromethyl Moieties

    Institute of Scientific and Technical Information of China (English)

    FEI Chun-Hong; PENG Zeng-Hui; LV Feng-Zhen; ZHANG Ling-Li; YAO Li-Shuang; XUAN Li

    2006-01-01

    @@ We investigate the liquid-crystal (LC) alignment direction on photoalignment films formed from photosensitive polyester containing thrifluoromethyl moieties (PPDA ) with various molecular weights by crossed polarized optical microscopy. It is found that LC alignment behaviour changes with molecular weight of PPDA. The LC alignment on PPDA irradiated films with the highest molecular weight is homogeneous, while those with low and intermediate molecular weights are homeotropic. However, surface morphologies show weak dependence on molecular weight. The surfaces are smooth and there is no clear morphological anisotropy on these aligned films observed by an atomic force microscope. The surface energies of the irradiated films are also measured by using an indirect contact-angle method where both surface energy and its polar componentincrease with increasing molecular weight. Different polar surface energies can be considered as a main reason for different alignment characteristics.

  19. Morphology, Crystallization, and Melting of Single Crystals and Thin Films of Star-branched Polyesters with Poly(ε-caprolactone) Arms as Revealed by Atomic Force Microscopy

    NARCIS (Netherlands)

    Nunez, E.; Vancso, G.J.; Gedde, U.W.

    2008-01-01

    The morphology and thermal stability of different sectors in solution- and melt-grown crystals of star-branched polyesters with poly(ε-caprolactone) (PCL) arms, and of a reference linear PCL, have been studied by tapping-mode atomic-force microscopy (AFM). Real-time monitoring of melt-crystallizati

  20. Thermal and Optical Properties of CdS Nanoparticles in Thermotropic Liquid Crystal Monomers

    Directory of Open Access Journals (Sweden)

    Marc Alnot

    2010-03-01

    Full Text Available Two new mesogenic monomers, namely 3,3’-dimethoxy-4,4’-di(hydroxyhexoxy-N-benzylidene-o-Tolidine (Ia and 4,4’-di(6-hydroxyhexoxy-N-benzylidene-o-Tolidine (IIa, were reacted with cadmium sulfide (CdS via an in situ chemical precipitation method in ethanol to produce CdS nanocomposites. A series of different mass compositions of CdS with Ia and IIa ranging from 0.1:1.0 to 1.0:1.0 (w/w were prepared and characterized using X-ray Diffraction (XRD, Raman spectroscopy, Fourier Transform Infrared Spectroscopy (FT-IR, Transmission Electron Microscopy (TEM, Polarizing Optical Microscopy (POM and Differential Scanning Calorimetry (DSC, X-ray Photoelectron Spectroscopy (XPS and Photoluminescence Spectroscopy (PL. XRD showed that the broad peaks are ascribed to the formation of cubic CdS nanoparticles in both Ia and IIa. The average particle size for both nanocomposites was less than 5 nm with a narrower size distribution when compared with pure CdS nanoparticles. The analyses from POM and DSC demonstrated that mass composition from 0.1:1.0 up to 0.5:1.0 of CdS:Ia nanocomposites showed their enantiotropic nematic phase. On the other hand, polarizing optical microscopy (POM for IIa nanocomposites showed that the liquid crystal property vanished completely when the mass composition was at 0.2:1.0. PL emissions for CdS: Ia or IIa nanocomposites indicated deep trap defects occurred in these both samples. The PL results revealed that addition of CdS to Ia monomers suppressed the photoluminescence intensity of Ia. However, the introduction of CdS to IIa monomers increased the photoluminescence and was at a maximum when the mass composition was 0.3:1.0, then decreased in intensity as more CdS was added. The XPS results also showed that the stoichiometric ratios of S/Cd were close to 1.0:1.0 for both types of nanocomposites for a mass composition of 1.0:1.0 (CdS:matrix.

  1. Polyester monomers lack ability to bind and activate both androgenic and estrogenic receptors as determined by in vitro and in silico methods.

    Science.gov (United States)

    Osimitz, Thomas G; Welsh, William J; Ai, Ni; Toole, Colleen

    2015-01-01

    The paper presents results from the screening of seven monomers used by Eastman Chemical to make various polymers. Ethylene glycol, diethylene glycol, polytetramethylene glycol, isophthalic acid, monosodium-5-sulfoisophthalic acid, 1,4-cyclohexanedicarboxylic acid, and dimethylcyclohexanedicarboxylate were screened for potential androgenicity or estrogenicity. The following studies were conducted: QSAR for binding to the AR and ER, in vitro Androgen Receptor Binding Assay, in vitro Estrogen Receptor Binding Assays (alpha and beta isoforms), in vitro Androgen Receptor Transactivation Assay in human cells, and in vitro Estrogen Receptor Transactivation Assay in human cells. None of the QSAR models predicted that any of the monomers possessed appreciable binding affinity for either AR or ER. Binding assays showed no evidence of interaction with either the AR or the alpha or beta ER receptors. Similarly, the AR and ER transactivation assays were negative. Moreover, six of the seven monomers have been subjected to 13-week and developmental toxicity studies in rats with no androgen- or estrogen-related effects being noted. Given the negative results of the in vitro screening assays (except PMG which demonstrated cytotoxicity) as well as available repeated dose and developmental and reproductive studies, the data suggest that none of the monomers tested exhibit androgenic or estrogenic hazards.

  2. Effect of sucrose polyesters on crystallization rate of vegetable ghee: solid fat content study

    Directory of Open Access Journals (Sweden)

    Ibrahim Nasir, Mohammad

    2003-12-01

    Full Text Available Crystallization rate of partial hydrogenated blend of soybean oil and cottonseed oil used for making vegetable ghee (vanaspati was investigated, by solid fat content (SFC using pulsed nuclear magnetic resonance (p-NMR. The effects of adding sucrose fatty acid esters or sucrose polyesters (SPE on the crystallization rate of the blend fat were studied. Sucrose tetrastearate DK ester F-10 (stearate 70% - palmitate 30% was added to the fat at different concentration, namely 0.5% and 1.0%. Blank sample and sample containing 0.5% and 1.0% DK ester F-10 / (DK F-10 were chosen to measure the change in SFC at constant temperature of 15ºC for a period of 25 hr. Five determinations of SFC were taken to the fat samples during the 25 hr i.e. 2,5,9,13 and 25th hr. SFC vs. time of crystallization of the three samples showed continuous increasing in SFC in all samples during the 25 hr, with sharp increasing at the first two hours. Samples containing 0.0% and 0.5% DK F-10, showed no significant difference in SFC during the first thirteen hours, while sample containing 1.0% DK F-10, showed higher SFC than the other two samples, through out the period. The amount of SFC for 1.0% DK F-10 sample at the 13th hour is equal to the SFC of the blank (0.0% sample at the 25th hour. Melting point of the same samples increased with the increasing DK F-10 concentration in the fat samples. The results of SFC make it sure that the addition of 1.0% DK F- 10 will shorten the time required for the crystallization of vegetable ghee while the addition of 0.5% will not have significant effect.Se ha investigado, mediante el contenido en grasa sólida (SFC por resonancia magnética nuclear pulsada (p-NMR, la velocidad de cristalización de mezcla de aceite de la soja y aceite de semilla del algodón parcialmente hidrogenada utilizada en la elaboración de ghee vegetal (vanaspati. Se han estudiado los efectos de añadir ésteres de sacarosa de ácidos grasos o poliésteres de

  3. Isothermal Cold Crystallization, Heat Resistance, and Tensile Performance of Polylactide/Thermoplastic Polyester Elastomer (PLA/TPEE) Blends: Effects of Annealing and Reactive Compatibilizer

    OpenAIRE

    Sisi Wang; Sujuan Pang; Lisha Pan; Nai Xu; Tan Li

    2016-01-01

    The combined influences of crystallinity and reactive compatibilizer—a multifunctional epoxide (ADR)—on morphology, tensile performance, and heat resistance of polylactide/thermoplastic polyester elastomer (PLA/TPEE) (80/20) blends were investigated. Annealing involved an isothermal cold crystallization of PLA matrix was performed to increase crystallinity of the samples. First, isothermal cold crystallization kinetics were investigated using differential scanning calorimetry measurement. It ...

  4. Organic Crystal Engineering of Thermosetting Cyanate Ester Monomers: Influence of Structure on Melting Point

    Science.gov (United States)

    2016-05-27

    heating baseline does show a modest non - linearity due to its nearness to the onset of the wide melting peak. Because we elected not to use heating...Guenthner, Sean M. Ramirez , Michael D. Ford, Denisse Soto, Jerry A. Boatz, Kamran B. Ghiassi and Joseph M. Mabry 5d. PROJECT NUMBER 5e. TASK...longer Si-C bonds for C-C bonds in the monomer chemical structure results in the “unlocking” of new degrees of freedom in non -interlocking molecules

  5. Degradation of microbial polyesters.

    Science.gov (United States)

    Tokiwa, Yutaka; Calabia, Buenaventurada P

    2004-08-01

    Microbial polyhydroxyalkanoates (PHAs), one of the largest groups of thermoplastic polyesters are receiving much attention as biodegradable substitutes for non-degradable plastics. Poly(D-3-hydroxybutyrate) (PHB) is the most ubiquitous and most intensively studied PHA. Microorganisms degrading these polyesters are widely distributed in various environments. Although various PHB-degrading microorganisms and PHB depolymerases have been studied and characterized, there are still many groups of microorganisms and enzymes with varying properties awaiting various applications. Distributions of PHB-degrading microorganisms, factors affecting the biodegradability of PHB, and microbial and enzymatic degradation of PHB are discussed in this review. We also propose an application of a new isolated, thermophilic PHB-degrading microorganism, Streptomyces strain MG, for producing pure monomers of PHA and useful chemicals, including D-3-hydroxycarboxylic acids such as D-3-hydroxybutyric acid, by enzymatic degradation of PHB.

  6. Synthesis and Properties of Hyperbranched Polyesters with Diol as a Core Monomer%二元醇为核单体的超支化聚酯的合成与性能

    Institute of Scientific and Technical Information of China (English)

    王勇; 朱延安; 孔霞; 瞿金清

    2013-01-01

      分别以乙基丁基丙二醇(BEPD)、1,4-丁二醇(BDO)和新戊二醇(NPG)为核单体,二羟甲基丙酸为AB2型单体,对甲苯磺酸为催化剂,采用准一步法合成了第三代超支化聚酯(HBP-1、HBP-2和HBP-3)。采用FT-IR、1H-NMR和GPC对其结构和分子量进行表征并测定了超支化聚酯的特性黏度。以甲苯二异氰酸酯加成物为固化剂,研究了超支化聚酯的固化涂膜性能,使用热重分析仪(TGA)考察了超支化聚酯涂膜的热稳定性能。结果表明,三种核单体成功合成了超支化聚酯,以BEPD为核单体的超支化聚酯HBP-1具有最高的支化度达到0.55。GPC测得的分子量与理论分子量接近,且以BEPD为核的HBP-1分子量分布最低为1.68。超支化聚酯在极性溶剂中有较好的溶解性能,在非极性溶剂中不溶,其中HBP-1具有更好的溶解性能和较低的特性黏度(4.24 mL⋅g−1)。超支化聚酯的固化涂膜具有较好的热稳定性、优异的附着力、柔韧性和较高的硬度。%  The third generation hyperbranched polyesters (HBPs) were synthesized by the pseudo-one step method with 2,2-bis(hydroxyl-methyl) propionic acid as AB2 monomer, p-toluene sulfonic acid as catalyst, in which 2-butyl-2-ethyl-1,3-propanediol (BEPD, HBP-1), 1,4-butanediol (BDO, HBP-2), and neopentyl glycol (NPG, HBP-3) were used as the core monomers, respectively. The structures and molecular weights of HBPs were characterized with FT-IR, NMR and GPC as well as their intrinsic viscosities were also given. The film properties of HBPs cured by the toluene diisocyanate adduct were tested. The thermal stability of cured HBPs films were also examined by thermogravimetric analysis (TGA). It was found that HBPs are successfully synthesized and HBP-1 displays the highest branching degree up to 0.55. The GPC measured molecular weights of HBPs approach to the theoretical values, and HBP-1 exhibits the lowest polydispersity index up to 1

  7. Influence of substitution on the optical properties of functionalized pentacene monomers and crystals: Experiment and theory

    KAUST Repository

    Saeed, Yasir

    2013-10-01

    The influence of solubilizing substitutional groups on the electronic structure of prototypical functionalized pentacene molecules and crystals is studied by a combined experimental and theoretical approach. We experimentally establish characteristic effects of substituents on the electronic structure and relate those to theoretical optical spectra in order to explain the experimental results and provide a comprehensive picture of the substitution effects. Bands associated to C/Si atoms connecting the functional side group to the pentacene in the (6,13)-positions are the main contributors to the optical transitions. The amplitude of the redshift between the crystals and molecules provides insight in the packing structure. © 2013 Elsevier B.V. All rights reserved.

  8. Effect of Silicon Substitution on the Crystal Properties of Cyanate Ester Monomers (Briefing Charts)

    Science.gov (United States)

    2015-08-17

    with 2 phr nonylphenol All samples were melted, blended, and de-gassed for 30 min. prior to cure in silicone molds under N2, cure schedule for 1 hr at...g ) Temperature (°C) BADCy (1st heating) BADCy (2nd Heating) Si-Containing Cyanate Esters: Non-isothermal DSC 9 114 kJ/mol Post- cure Tg: 305 °C BADCy...Charts 3. DATES COVERED (From - To) July 2015-August 2015 4. TITLE AND SUBTITLE EFFECT OF SILICON SUBSTITUTION ON THE CRYSTAL PROPERTIES OF

  9. Reinvestigation on the Reaction of Salicylic Chloride with Salicylic Amide and X-ray Crystal Structure of a New Macrocyclic Polyester

    Institute of Scientific and Technical Information of China (English)

    DU Da-Ming; CHEN Xiao; HUA Wen-Ting; JIN Xiang-Lin

    2003-01-01

    The reaction of salicylic chloride and salicylic amide at 170 ℃ gave benzoxazine and a new macrocyclic polyester 3, whose crystal structure has been determined by single-crystal X-ray diffraction analysis. Compound 3: C28H16O8, Mr = 480.41, monoclinic, space group P21/n, a = 15.353(3), b = 14.196(3), c = 21.147(4) A, β = 103.32(3)°, V = 4485(2) A3, Z = 8, F(000) = 1984, Dc = 1.423 g/cm3 and μ = 0.106 mm-1. The final R = 0.0535 and Wr = 0.1275 for 7903 observed reflections (I ≥ 2σ(I)). In the asymmetric unit of the compound there exist two independent molecules which are connected by weak aromatic C-H…O hydrogen bonding between C(47)- H(47) and atom O(7) of the carbonyl group.

  10. Self-assembly and UV-curing Property of Polymerized Lyotropic Liquid Crystal Monomer of Sodium 3,4,5-tris(11-acryloxyundecyloxy)benzoate

    Institute of Scientific and Technical Information of China (English)

    Yu-qin Bai; Jin-bao Guo; Ying Wang; Jie Wei

    2013-01-01

    A polymerized lyotropic liquid crystal monomer of sodium 3,4,5-tris (11-acryloxyundecyloxy)benzoate was synthesized by a convenient route starting from 3,4,5-trihydroxybenzoic acid via esterification followed by etherification,acylation and finally neutralization.The chemical structure was confirmed by Fourier transform infrared (FT-IR) and 1H nuclear magnetic resonance spectral analysis.The self-organization behavior of the monomer with deionized water in methanol at room temperature was also demonstrated.The assemblies were characterized by polarized optical microscope and X-ray diffraction.The results show that a solution containing 80∶20 of the monomer to water was found to be able to self-organize into Lamellar (La) phase and 92∶8 with inverted hexagonal (HⅡ) phase,which was in accordance with the theoretical calculation of critical packing parameter.It suggests that the concentration of the monomer was the key factor to influence assembly structure.Additionally,the acrylate conversion with different photoinitiators and nanostructure retention after polymerization were investigated.The research shows that the acrylate conversion of the monomer with Darocur2959 could reach up to 78% when irradiated by 30 mW/cm2 UV light of 365 nm for 30 min characterized by Real-time FT-IR as well as the sol-gel method.Meanwhile,the La and HⅡI phase nanostructures were both retained after polymerization.

  11. Isothermal Cold Crystallization, Heat Resistance, and Tensile Performance of Polylactide/Thermoplastic Polyester Elastomer (PLA/TPEE Blends: Effects of Annealing and Reactive Compatibilizer

    Directory of Open Access Journals (Sweden)

    Sisi Wang

    2016-12-01

    Full Text Available The combined influences of crystallinity and reactive compatibilizer—a multifunctional epoxide (ADR—on morphology, tensile performance, and heat resistance of polylactide/thermoplastic polyester elastomer (PLA/TPEE (80/20 blends were investigated. Annealing involved an isothermal cold crystallization of PLA matrix was performed to increase crystallinity of the samples. First, isothermal cold crystallization kinetics were investigated using differential scanning calorimetry measurement. It was found that the addition of ADR decreased the crystallization rate of the samples. The maximum crystallinity of the annealed samples also decreased from 40% to 34% while ADR loading increased from zero to 1.0 phr. Furthermore, influence of crystallinity on mechanical performances of the PLA/TPEE sample was researched. The heat resistance of the sample showed a significant enhancement while increasing its crystallinity. Meanwhile, the tensile ductility of the crystallized PLA/TPEE sample became very poor due to the embrittlement with increased crystallinity and the incompatibility between PLA and TPEE. However, the annealed PLA/TPEE/ADR samples with high crystallinity kept a higher tensile ductility because ADR greatly improved the interfacial compatibility. Differences in tensile fracture behaviors of the quenched and annealed PLA/TPEE samples with and without ADR were discussed in detail. At last, crystallized PLA/TPEE/ADR blends with excellent heat resistance and high tensile ductility were obtained by annealing and reactive compatibilization.

  12. From polymer to monomer: cleavage and rearrangement of Si-O-Si bonds after oxidation yielded an ordered cyclic crystallized structure.

    Science.gov (United States)

    Zuo, Yujing; Gou, Zhiming; Cao, Jinfeng; Yang, Zhou; Lu, Haifeng; Feng, Shengyu

    2015-07-27

    Polymerization reactions are very common in the chemical industry, however, the reaction in which monomers are obtained from polymers is rarely invesitgated. This work reveals for the first time that oxone can break the Si-O-Si bond and induce further rearrangement to yield an ordered cyclic structure. The oxidation of P1, which is obtained by reaction of 2,2'-1,2-ethanediylbis(oxy)bis(ethanethiol) (DBOET) with 1,3-divinyl-1,1,3,3-tetramethyldisiloxane (MM(Vi)), with oxone yielded cyclic crystallized sulfone-siloxane dimer (P1-ox) after unexpected cleavage and rearrangement of the Si-O-Si bond.

  13. Biocatalytic synthesis of silicone polyesters.

    Science.gov (United States)

    Frampton, Mark B; Subczynska, Izabela; Zelisko, Paul M

    2010-07-12

    The immobilized lipase B from Candida antarctica (CALB) was used to synthesize silicone polyesters. CALB routinely generated between 74-95% polytransesterification depending on the monomers that were used. Low molecular weight diols resulted in the highest rates of esterification. Rate constants were determined for the CALB catalyzed polytransesterifications at various reaction temperatures. The temperature dependence of the CALB-mediated polytransesterifications was examined. A lipase from C. rugosa was only successful in performing esterifications using carboxy-modified silicones that possessed alkyl chains greater than three methylene units between the carbonyl and the dimethylsiloxy groups. The proteases alpha-chymotrypsin and papain were not suitable enzymes for catalyzing any polytransesterification reactions.

  14. An Undergraduate Experiment in Polyester (PET) Synthesis

    Science.gov (United States)

    Cammidge, Andrew N.

    1999-02-01

    The most important polyester manufactured industrially is PET (polyethyleneterephthalate). We describe an experiment that conveniently mimics the industrial synthesis in the undergraduate laboratory. The first step of the reaction is a base-catalyzed transesterification between ethane diol and dimethylterephthalate. Methanol is distilled off to drive the reaction to completion. Excess ethane diol is employed to suppress formation of higher oligomers. The intermediate (bis-(2-hydroxyethyl)terephthalate) is isolated by crystallization and filtration and characterized by 1H NMR spectroscopy. In the second step the monomer is heated (with and without acid catalyst) to form polymer. Samples are removed at intervals and their physical properties are recorded as they cool. These properties are used to qualitatively monitor polymerization. This experiment reinforces some fundamental chemical concepts and introduces the students to new laboratory procedures. The students perform a distillation and apply their knowledge of the reaction equilibrium to calculate the volume of distillate (methanol) expected. The reversible nature of esterification reactions is emphasized during the polymerization step (acid-catalyzed), where the process is driven towards polymer formation by the removal (evaporation) of ethane diol.

  15. The Crystal and Molecular Structure of an Asymmetric Diacetylene Monomer, 6-(2-methyl-4-nitroanilino)-2,4-hexadiyne-1-ol

    Science.gov (United States)

    Vlasse, Marcus; Paley, Mark S.

    1993-01-01

    The crystal and molecular structure of an asymmetric diacetylene monomer has been determined from x-ray diffraction data. The crystals, obtained from an acetone/pentane solution, are orthorhombic, Fdd2 with Z = 16 in a unit cell having dimensions of a = 42.815(6) A, b = 22.224(5) A, c = 4.996(l) A. The structure was solved by direct methods and refined by least- squares techniques to an R(sub F) of 6.4% for 988 reflections and 171 variables. The diacetylene chains are disposed in the unit cell in a complex manner in order to satisfy the hydrogen- bonding, crystal packing, and symmetry requirements of the system. The solid state polymerization mechanism is discussed with respect to the geometric disposition of the diacetylene chains. These chains are far apart and incorrectly oriented with respect to each other to permit polymerization in the crystal by means of 1,4-addition, consistent with the Baughman mechanistic model.

  16. Fully Biobased Unsaturated Aliphatic Polyesters from Renewable Resources : Enzymatic Synthesis, Characterization, and Properties

    NARCIS (Netherlands)

    Jiang, Yi; Alberda van Ekenstein, Gerhard; Woortman, Albert J. J.; Loos, Katja

    2014-01-01

    Fully biobased saturated and unsaturated aliphatic polyesters and oligoesters are successfully prepared by Candida antarctica lipase B (CALB)-catalyzed polycondensations of succinate, itaconate, and 1,4-butanediol. The effects of monomer substrates and polymerization methods on enzymatic polycondens

  17. Fully Biobased Unsaturated Aliphatic Polyesters from Renewable Resources : Enzymatic Synthesis, Characterization, and Properties

    NARCIS (Netherlands)

    Jiang, Yi; Alberda van Ekenstein, Gerhard; Woortman, Albert J. J.; Loos, Katja

    2014-01-01

    Fully biobased saturated and unsaturated aliphatic polyesters and oligoesters are successfully prepared by Candida antarctica lipase B (CALB)-catalyzed polycondensations of succinate, itaconate, and 1,4-butanediol. The effects of monomer substrates and polymerization methods on enzymatic

  18. Novel organometallic aromatic polyester based on ferrocene

    Institute of Scientific and Technical Information of China (English)

    Wei

    2010-01-01

    A novel polyester containing ferrocenyl was prepared by low-temperature interface polycondensation of 1,1'-ferrocenedi-carboxylic acid chloride with 4-(4-hydroxyphenyl)-2,3-phthalazin-l-one(DHPZ), which is a twisted non-coplanar heterocyclic bisphenol-like monomer. The newly generated polymer was evaluated based on characterization of its solubility, viscosity measurements, elemental analysis, FTIR spectroscopy, differential scanning calorimetric and thermogravimetric studies.

  19. Synthesis and Characterization of Aliphatic-Aromatic Hyperbranched Polyesters

    Institute of Scientific and Technical Information of China (English)

    唐黎明; 张晓龙; 邱藤; 刘德山

    2002-01-01

    Hyperbranched polymers possess special architectures and have potential applications in various areas. In this study, two AB2 monomers, dipropyl 5-(hydroxyethoxy) isophthalate (I) and 5-hydroxyethoxyisophthaic acid (II), were prepared. By bulk polycondensation of each monomer, two aliphatic-aromatic hyperbranched polyesters were prepared and characterized by 1H-nuclear magnetic resonance (1H-NMR), differential scanning calorimetry (DSC), thermogravimetry analysis (TGA), and scanning electron microscopy (SEM). Compared with all-aromatic hyperbranched polyesters, the prepared polymers showed lower glass transition temperatures in connection with the moderate decrease in their decomposition temperatures.

  20. Study on Alternating Copolymerization of Polyester-amides

    Institute of Scientific and Technical Information of China (English)

    WEI Wen-liang; LI Jian-mei; ZHU Fang-liang

    2002-01-01

    The preparing methods, choice of catalysts and reaction kinetics of one of the monomers, diesteramide(DEA), of polyester-amides were investigated in details. The chemical structure of DEA was analyzed. And the Polyester-amides (PEA) were obtained by melt copolymerization with DEA. It is shown that DEA can be synthesized by DMT and hexamethylene diamine with the catalyst EX - 1 or EX - 2. The relationship between reaction rate of synthesizing monomer and concentration of hexamethylene diamine is first order kinetic relation.

  1. Enhancement of Adhesion between EPDM and Polyester Fabric by Using Natural Rubber Modified by Maleic Anhydride

    Directory of Open Access Journals (Sweden)

    A. A. El-Wakil

    2011-01-01

    Full Text Available This study presents a new method for improving adhesion between ethylene propylene diene monomer (EPDM rubber and polyester fabric. In this work, natural rubber was modified by maleic anhydride in order to improve the adhesion force between ethylene propylene diene monomer rubber and polyester fabric. The effect of thermal aging and ionizing radiation on the stability of the rubber mix as well as on the peel strength of the rubber-coated fabric was investigated. It was observed that the natural rubber modified by maleic anhydride improved the peel strength of the EPDM rubber-coated polyester fabric.

  2. Design of Functional Polyesters for Electronic and Biological Applications

    OpenAIRE

    Nelson, Ashley Marie

    2015-01-01

    Melt polymerization and novel monomers enabled the synthesis of polyesters for electronic and biological applications. Inspiration from nature and a passion for environmental preservation instigated an emphasis on the incorporation of renewable resources into polymeric materials. Critical analysis of current research surrounding bisphenol-A replacements and ion-containing segmented polyurethanes aided in identifying benchmark polymers, including limitations, challenges, and future needs. S...

  3. Liquid Crystalline Furandicarboxylic Acid-based Aaromatic Polyesters

    NARCIS (Netherlands)

    WILSENS, CAROLUS HENRICUS R. MARIA; RASTOGI, SANJAY; VELD, MARTIJN ARNOLDUS JOHANNES; KLOP, ENNO ANTON; NOORDOVER, BART ADRIANUS JOHANNES

    2013-01-01

    The invention pertains to a fully aromatic liquid crystalline furandicarboxylic acid- based aromatic polyester obtainable from a mixture of monomers comprising 2,5- furandicarboxylic acid, p-hydroxybenzoic acid, an aromatic diol, and 5-40 mol% of an aromatic monocarboxylic acid selected from vanilli

  4. Biochemical and Structural Insights into Enzymatic Depolymerization of Polylactic Acid and Other Polyesters by Microbial Carboxylesterases.

    Science.gov (United States)

    Hajighasemi, Mahbod; Nocek, Boguslaw P; Tchigvintsev, Anatoli; Brown, Greg; Flick, Robert; Xu, Xiaohui; Cui, Hong; Hai, Tran; Joachimiak, Andrzej; Golyshin, Peter N; Savchenko, Alexei; Edwards, Elizabeth A; Yakunin, Alexander F

    2016-06-13

    Polylactic acid (PLA) is a biodegradable polyester derived from renewable resources, which is a leading candidate for the replacement of traditional petroleum-based polymers. Since the global production of PLA is quickly growing, there is an urgent need for the development of efficient recycling technologies, which will produce lactic acid instead of CO2 as the final product. After screening 90 purified microbial α/β-hydrolases, we identified hydrolytic activity against emulsified PLA in two uncharacterized proteins, ABO2449 from Alcanivorax borkumensis and RPA1511 from Rhodopseudomonas palustris. Both enzymes were also active against emulsified polycaprolactone and other polyesters as well as against soluble α-naphthyl and p-nitrophenyl monoesters. In addition, both ABO2449 and RPA1511 catalyzed complete or extensive hydrolysis of solid PLA with the production of lactic acid monomers, dimers, and larger oligomers as products. The crystal structure of RPA1511 was determined at 2.2 Å resolution and revealed a classical α/β-hydrolase fold with a wide-open active site containing a molecule of polyethylene glycol bound near the catalytic triad Ser114-His270-Asp242. Site-directed mutagenesis of both proteins demonstrated that the catalytic triad residues are important for the hydrolysis of both monoester and polyester substrates. We also identified several residues in RPA1511 (Gln172, Leu212, Met215, Trp218, and Leu220) and ABO2449 (Phe38 and Leu152), which were not essential for activity against soluble monoesters but were found to be critical for the hydrolysis of PLA. Our results indicate that microbial carboxyl esterases can efficiently hydrolyze various polyesters making them attractive biocatalysts for plastics depolymerization and recycling.

  5. The use of DSC to study isothermal crystallization behavior of super bright polyester chips with high intrinsic viscosity%DSC法研究高粘度超有光聚酯切片的等温结晶

    Institute of Scientific and Technical Information of China (English)

    王玉合; 王树霞; 司虎; 戴钧明

    2012-01-01

    The crystallization behavior of PET with different intrinsic viscosity was investigated using differential scanning calorimetry(DSC).The results show that the cold crystallization peaks(T c) increased and the melting crystallization peaks(T mc) decreased with the intrinsic viscosity increasing.It also shows that Avrami equation was satisfying in describing the isothermal crystallization kinetics of polyesters.Half-time crystallization t 1 /2 increased with the intrinsic viscosity increasing in the same crystallization temperature.These illustrated PET crystallization speed decreased with the intrinsic viscotisy increasing.%采用差示扫描量热法(DSC)对自制不同特性粘数的超有光聚酯切片进行结晶行为研究。分析结果表明:特性粘数增加,冷结晶温度Tc升高,熔融结晶温度Tmc降低,即结晶变慢;等温结晶行为较好地符合了Avrami方程。在同样的结晶温度下,特性粘数升高,半结晶周期t1/2增加,结晶变慢;相同时间内随着聚酯样品特性粘数的升高,结晶速率变慢。

  6. Bio-based liquid crystalline polyesters

    Science.gov (United States)

    Wilsens, Carolus; Rastogi, Sanjay; Dutch Collaboration

    2013-03-01

    The reported thin-film polymerization has been used as a screening method in order to find bio-based liquid crystalline polyesters with convenient melting temperatures for melt-processing purposes. An in depth study of the structural, morphological and chemical changes occurring during the ongoing polycondensation reactions of these polymers have been performed. Structural and conformational changes during polymerization for different compositions have been followed by time resolved X-ray and Infrared spectroscopy. In this study, bio-based monomers such as vanillic acid and 2,5-furandicarboxylic acid are successfully incorporated in liquid crystalline polyesters and it is shown that bio-based liquid crystalline polymers with high aromatic content and convenient processing temperatures can be synthesized. Special thanks to the Dutch Polymer Institute for financial support

  7. Cutin and suberin monomers are membrane perturbants.

    Science.gov (United States)

    Douliez, Jean-Paul

    2004-03-15

    The interaction between cutin and suberin monomers, i.e., omega -hydroxylpalmitic acid, alpha, omega -hexadecanedioic acid, alpha, omega --hexadecanediol, 12-hydroxylstearic acid, and phospholipid vesicles biomimicking the lipid structure of plant cell membranes has been studied by optical and transmission electron microscopy, quasielastic light scattering, differential scanning calorimetry, and (31)P solid-state NMR. Monomers were shown to penetrate model membranes until a molar ratio of 30%, modulating their gel to fluid-phase transition, after which monomer crystals also formed in solution. These monomers induced a decrease of the phospholipid vesicle size from several micrometers to about 300 nm. The biological implications of these findings are discussed.

  8. Enzyme-catalysis breathes new life into polyester condensation polymerizations.

    Science.gov (United States)

    Gross, Richard A; Ganesh, Manoj; Lu, Wenhua

    2010-08-01

    Traditional chemical catalysts for polyester synthesis have enabled the generation of important commercial products. Undesirable characteristics of chemically catalyzed condensation polymerizations include the need to conduct reactions at high temperatures (150-280 degrees C) with metal catalysts that are toxic and lack selectivity. The latter is limiting when aspiring towards synthesis of increasingly complex and well-defined polyesters. This review describes an exciting technology that makes use of immobilized enzyme-catalysts for condensation polyester synthesis. Unlike chemical catalysts, enzymes function under mild conditions (< or =100 degrees C), which enables structure retention when polymerizing unstable monomers, circumvents the introduction of metals, and also provides selectivity that avoids protection-deprotection steps and presents unique options for structural control. Examples are provided that describe the progress made in enzyme-catalyzed polymerizations, as well as current limitations and future prospects for developing more efficient enzyme-catalysts for industrial processes.

  9. Biosynthesis of Polyhydroxyalkanoates Consisting of Short-chain-length Monomers and Medium-chain-length Monomers by Pseudomonas YS1

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    A strain capable of producing polyhydroxyalkanoates (PHAs) consisting of short- and medium-chain-length monomers was identified as Pseudomonas sp.coded as YS1.The strain synthesized PHAs containing monomers of hydroxybutyrate(HB or C4) and/or hydroxyoctanoate (HO or C8) and/or hydroxydecanoate (HD or C10) when grown in various substrates including glucose, raw sugar, molasses and various fatty acids.It was found that growth temperature affected the HB and HO monomer contents in the PHA.HB content in PHA increased from mole fraction 69% at 26℃ to mole fraction 85% at 37℃ while HO content decreased from mole fraction 29% at 26℃ to mole fraction 12% at 37℃.The temperature effect provides a simple and effective way to control the PHA composition and hence control the PHA mechanical and other physical properties.Also, the fermentor experiment indicated that PHB formation was growth associated and HO monomer production was in fact promoted by N-limitation.This conclusion was further supported by the fact that the formation of PHB only polyester was observed only when C/N molar ratio was smaller than 20.Higher C/N ratio led to the formation of HO monomers in the polyesters.

  10. Recovery of olefin monomers

    Science.gov (United States)

    Golden, Timothy Christoph; Weist, Jr., Edward Landis; Johnson, Charles Henry

    2004-03-16

    In a process for the production of a polyolefin, an olefin monomer is polymerised said polyolefin and residual monomer is recovered. A gas stream comprising the monomer and nitrogen is subjected to a PSA process in which said monomer is adsorbed on a periodically regenerated silica gel or alumina adsorbent to recover a purified gas stream containing said olefin and a nitrogen rich stream containing no less than 99% nitrogen and containing no less than 50% of the nitrogen content of the gas feed to the PSA process.

  11. Aliphatic polyester block polymers: renewable, degradable, and sustainable.

    Science.gov (United States)

    Hillmyer, Marc A; Tolman, William B

    2014-08-19

    Nearly all polymers are derived from nonrenewable fossil resources, and their disposal at their end of use presents significant environmental problems. Nonetheless, polymers are ubiquitous, key components in myriad technologies and are simply indispensible for modern society. An important overarching goal in contemporary polymer research is to develop sustainable alternatives to "petro-polymers" that have competitive performance properties and price, are derived from renewable resources, and may be easily and safely recycled or degraded. Aliphatic polyesters are particularly attractive targets that may be prepared in highly controlled fashion by ring-opening polymerization of bioderived lactones. However, property profiles of polyesters derived from single monomers (homopolymers) can limit their applications, thus demanding alternative strategies. One such strategy is to link distinct polymeric segments in an A-B-A fashion, with A and B chosen to be thermodynamically incompatible so that they can self-organize on a nanometer-length scale and adopt morphologies that endow them with tunable properties. For example, such triblock copolymers can be useful as thermoplastic elastomers, in pressure sensitive adhesive formulations, and as toughening modifiers. Inspired by the tremendous utility of petroleum-derived styrenic triblock copolymers, we aimed to develop syntheses and understand the structure-property profiles of sustainable alternatives, focusing on all renewable and all readily degradable aliphatic polyester triblocks as targets. Building upon oxidation chemistry reported more than a century ago, a constituent of the peppermint plant, (-)-menthol, was converted to the ε-caprolactone derivative menthide. Using a diol initiator and controlled catalysis, menthide was polymerized to yield a low glass transition temperature telechelic polymer (PM) that was then further functionalized using the biomass-derived monomer lactide (LA) to yield fully renewable PLA

  12. A critical review of algal biomass: A versatile platform of bio-based polyesters from renewable resources.

    Science.gov (United States)

    Noreen, Aqdas; Zia, Khalid Mahmood; Zuber, Mohammad; Ali, Muhammad; Mujahid, Mohammad

    2016-05-01

    Algal biomass is an excellent renewable resource for the production of polymers and other products due to their higher growth rate, high photosynthetic efficiency, great potential for carbon dioxide fixation, low percentage of lignin and high amount of carbohydrates. Algae contain unique metabolites which are transformed into monomers suitable for development of novel polyesters. This review article mainly focuses on algal bio-refinery concept for polyester synthesis and on exploitation of algae-based biodegradable polyester blends and composites in tissue engineering and controlled drug delivery system. Algae-derived hybrid polyester scaffolds are extensively used for bone, cartilage, cardiac and nerve tissue regeneration due to their biocompatibility and tunable biodegradability. Microcapsules and microspheres of algae-derived polyesters have been used for controlled and continuous release of several pharmaceutical agents and macromolecules to produce humoral and cellular immunity with efficient intracellular delivery. Copyright © 2016 Elsevier B.V. All rights reserved.

  13. Lipase-catalyzed polyester synthesis--a green polymer chemistry.

    Science.gov (United States)

    Kobayashi, Shiro

    2010-01-01

    This article is a short comprehensive review describing in vitro polyester synthesis catalyzed by a hydrolysis enzyme of lipase, most of which has been developed for these two decades. Polyesters are prepared by repeated ester bond-formation reactions; they include two major modes, ring-opening polymerization (ROP) of cyclic monomers such as cyclic esters (lactones) and condensation polymerization via the reaction between a carboxylic acid or its ester group and an alcohol group. Polyester synthesis is, therefore, a reaction in reverse way of in vivo lipase catalysis of ester bond-cleavage with hydrolysis. The lipase-catalyzed polymerizations show very high chemo-, regio-, and enantio-selectivities and involve various advantageous characteristics. Lipase is robust and compatible with other chemical catalysts, which allows novel chemoenzymatic processes. New syntheses of a variety of functional polyesters and a plausible reaction mechanism of lipase catalysis are mentioned. The polymerization characteristics are of green nature currently demanded for sustainable society, and hence, desirable for conducting 'green polymer chemistry'.

  14. Lipase-catalyzed polyester synthesis – A green polymer chemistry

    Science.gov (United States)

    Kobayashi, Shiro

    2010-01-01

    This article is a short comprehensive review describing in vitro polyester synthesis catalyzed by a hydrolysis enzyme of lipase, most of which has been developed for these two decades. Polyesters are prepared by repeated ester bond-formation reactions; they include two major modes, ring-opening polymerization (ROP) of cyclic monomers such as cyclic esters (lactones) and condensation polymerization via the reaction between a carboxylic acid or its ester group and an alcohol group. Polyester synthesis is, therefore, a reaction in reverse way of in vivo lipase catalysis of ester bond-cleavage with hydrolysis. The lipase-catalyzed polymerizations show very high chemo-, regio-, and enantio-selectivities and involve various advantageous characteristics. Lipase is robust and compatible with other chemical catalysts, which allows novel chemo-enzymatic processes. New syntheses of a variety of functional polyesters and a plausible reaction mechanism of lipase catalysis are mentioned. The polymerization characteristics are of green nature currently demanded for sustainable society, and hence, desirable for conducting ‘green polymer chemistry’. PMID:20431260

  15. Preparation and properties of high storage stability polyester polyol dispersion for two-component waterborne polyurethane coating

    Science.gov (United States)

    Hao, H.; Hu, J. Q.; Wang, F.; Tu, W. P.

    2017-01-01

    A new type of polyester polyol dispersion with good storage stability was prepared based on a hydrophilic monomer 5-sodium sulfodimethyl isophthalate (5-SIPM), and frequently-used monomers such as neopentyl glycol (NPG), dimethyl terephthalate (DMT), dimethyl phthalate (DMP) and trimethylolpropane (TMP) by the transpolycondensation and polycondensation method. The polyester polyol dispersion was characterized by FTIR and GPC. The proper content of these monomers were determined by the performance of polyester dispersion: the content of TMP was 15wt%, the content of NPG was 7.5wt% and the hydrophilic monomer 5-SIPM content was 5wt%. Two-component waterborne polyurethane (2K-WPU) coatings were prepared by Bayhydur® XP2487/1 and polyester polyol dispersions, which were stored before and after at 40 ° for 6 weeks, the prepared films have no differences in drying time, adhesion, pencil hardness, gloss and chemical resistance, the result also reveals that the polyester polyol dispersion have excellent storage stability resistance.

  16. SYNTHESIS AND CHARACTERIZATION OF Si-CONTAINING POLYESTER-POLYETHER MULTIBLOCK COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    LI Zhenyi; ZHU Jin

    1996-01-01

    A series of Si-containing polyester-polyether multiblock copolymers were synthesized by transesterification and melt copolycondensation of organosilicon monomers [1, 1, 3, 3-tetramethyl-1, 3-bis (p-carbomethoxyphenyl) disiloxane] (I) or dimethyl bis (p-carbomethoxyphenyl) silane] (II) and dimethyl terephthalate (DMT), with 1, 4-butanediol, polytetramethylene glycol (PTMG) respectively. The organosilicon monomers were prepared by Grinard reaction, oxidation and esterification. The structures of the above monomers (Ⅰ), (Ⅱ) and the copolymers were characterized by MS anal. and 1H-NMR.

  17. 21 CFR 177.1590 - Polyester elastomers.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyester elastomers. 177.1590 Section 177.1590... Components of Single and Repeated Use Food Contact Surfaces § 177.1590 Polyester elastomers. The polyester...) For the purpose of this section, polyester elastomers are those produced by the ester...

  18. Functional bio-based polyesters by enzymatic polymerization

    DEFF Research Database (Denmark)

    Daugaard, Anders Egede; Hoffmann, Christian; Andersen, Christian

    During recent years enzymatic polymerization has become increasingly popular as an alternative to classical polyesterification processes. The high regioselectivity observed for lipases permits preparation of novel polyesters with a high number of functional groups.1 This is particularly interesting...... polymerization was applied to prepare functional water soluble polyesters based on dimethyl itaconate and poly(ethyleneglycol).2 The monomer permits postfunctionalization using thiol-ene chemistry or aza-michael additions, which was used to illustrate the possibilites of preparing functional hydrogels. Hydrogels...... was copolymerized together with ethyl-6-hydroxyhexanoate yielding copolymers with molecular weights of up to 12,000 g/mol. The polymers were postfunctionalized using trifluoroacetic anhydride, which resulted in 100% conversion of the secondary alcohols, illustrating the possibility to use the secondary alcohol...

  19. Synthetic polyester from algae oil.

    Science.gov (United States)

    Roesle, Philipp; Stempfle, Florian; Hess, Sandra K; Zimmerer, Julia; Río Bártulos, Carolina; Lepetit, Bernard; Eckert, Angelika; Kroth, Peter G; Mecking, Stefan

    2014-06-23

    Current efforts to technically use microalgae focus on the generation of fuels with a molecular structure identical to crude oil based products. Here we suggest a different approach for the utilization of algae by translating the unique molecular structures of algae oil fatty acids into higher value chemical intermediates and materials. A crude extract from a microalga, the diatom Phaeodactylum tricornutum, was obtained as a multicomponent mixture containing amongst others unsaturated fatty acid (16:1, 18:1, and 20:5) phosphocholine triglycerides. Exposure of this crude algae oil to CO and methanol with the known catalyst precursor [{1,2-(tBu2 PCH2)2C6H4}Pd(OTf)](OTf) resulted in isomerization/methoxycarbonylation of the unsaturated fatty acids into a mixture of linear 1,17- and 1,19-diesters in high purity (>99 %). Polycondensation with a mixture of the corresponding diols yielded a novel mixed polyester-17/19.17/19 with an advantageously high melting and crystallization temperature.

  20. Modification of Biodegradable Polyesters Using Electron Beam

    Directory of Open Access Journals (Sweden)

    M. Suhartini

    2013-12-01

    Full Text Available Poly(4-Hydroxybutirat P4HB, Poly(butylene succinate-co-adipate PBSA and Poly(-caprolactone PCL were electron beam (EB-irradiated. Poly(4-Hydroxybutirat 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.

  1. Pressure polymerization of polyester

    Science.gov (United States)

    Maurer, Charles J.; Shaw, Gordon; Smith, Vicky S.; Buelow, Steven J.; Tumas, William; Contreras, Veronica; Martinez, Ronald J.

    2000-08-29

    A process is disclosed for the preparation of a polyester polymer or polyester copolymer under superatmospheric pressure conditions in a pipe or tubular reaction under turbannular flow conditions. Reaction material having a glycol equivalents to carboxylic acid equivalents mole ratio of from 1.0:1 to 1.2:1, together with a superatmospheric dense gaseous medium are fed co-currently to the reactor. Dicarboxylic acid and/or diol raw materials may be injected into any of the reaction zones in the process during operation to achieve the overall desired mole ratio balance. The process operates at temperatures of from about 220.degree. C. to about 320.degree. C., with turbannular flow achieved before the polymer product and gas exit the reactor process. The pressure in the reaction zones can be in the range from 15 psia to 2500 psia. A polymer product having a DP of a greater than 40, more preferably at least about 70, is achieved by the transfer of water from the reacting material polymer melt to the gaseous medium in the reactor.

  2. Synthesis of Functional Polyester Based on Polylactic Acid and Its Effect on PC12 Cells after Coupling with Small Peptides

    Directory of Open Access Journals (Sweden)

    Na Qiang

    2016-01-01

    Full Text Available Polyesters containing functional groups are a suitable candidate matrix for cell culture in tissue engineering. Three types of semicrystalline copolymer poly(L-lactide-co-β-malic acid [P(LA-co-BMD] with pendent carboxyl groups were synthesized in this study. The functional monomer 3(S-[(benzyloxycarbonylmethyl]-1,4-dioxane-2,5-dione (BMD was synthesized using L-aspartic acid. The copolymer P(LA-co-BMD was then synthesized through ring-opening copolymerization of L-LA and BMD, with dodecanol as initiator and stannous octoate as catalyst. Copolymer structure was characterized by 1H nuclear magnetic resonance (1H NMR, gel permeation chromatography (GPC, and differential scanning calorimetry (DSC analyses. Results of 1H NMR and GPC analyses showed that the copolymers were synthesized successfully. DSC curves showed that the crystal melting peak and enthalpy decreased with increased BMD. The crystallinity of the copolymer was destroyed by the presence of the functional monomer. After deprotection, carboxyl groups were coupled with the isoleucine-lysine-valine-alanine-valine peptide through N-hydroxysuccinimide/dicyclohexylcarbodiimide method. The small peptide was beneficial to the axon growth of PC12 cells.

  3. Cell debris self-immobilized thermophilic lipase: a biocatalyst for synthesizing aliphatic polyesters.

    Science.gov (United States)

    Sun, Yang; Yang, Yan; Wang, Chenhui; Liu, Jiaming; Shi, Wei; Zhu, Xiaobo; Lu, Laijin; Li, Quanshun

    2013-05-01

    The paper explored the catalytic activity of a cell debris self-immobilized thermophilic lipase for polyester synthesis, using the ring-opening polymerization of ε-caprolactone as model. Effects of biocatalyst concentration, temperature, and reaction medium on monomer conversion and product molecular weight were systematically evaluated. The biocatalyst displayed high catalytic activity at high temperatures (70-90 °C), with 100 % monomer conversion. High monomer conversion values (>90 %) were achieved in both hydrophobic and hydrophilic solvents, and also in solvent-free system, with the exception of dichloromethane. Poly(ε-caprolactone) was obtained in 100 % monomer conversion, with a number-average molecular weight of 1,680 g/mol and a polydispersity index of 1.35 in cyclohexane at 70 °C for 72 h. Furthermore, the biocatalyst exhibited excellent operational stability, with monomer conversion values exceeding 90 % over the course of 15 batch reactions.

  4. SYNTHESIS OF AN EPOXY-TERMINATED HYPERBRANCHED AROMATIC POLYESTER

    Institute of Scientific and Technical Information of China (English)

    Xia Wang; W.J. Feast

    2002-01-01

    An epoxy-terminated hyperbranched aromatic polyester (P3) was synthesized from a hyperbranched aromaticpolyester containing carboxylic acid end groups (P1), which was derived from the condensation polymerization of the AB2monomer, 5-acetoxyisophthalic acid. Polymer P1 was converted into the polymeric acid chloride by reaction with thionylchloride. The acid chloride was reacted with ethanol and glycidol to form a poly(ethyl ester) (P2) and an epoxy terminatedmaterial (P3), respectively. The reaction conditions in each step of these processes had to be controlled very carefully toavoid unwanted cross-linking reactions. The characterization of products and intermediates, including molecular weightdistributions and thermal properties, are reported.

  5. Kinetics of monomer biodegradation in soil.

    Science.gov (United States)

    Siotto, Michela; Sezenna, Elena; Saponaro, Sabrina; Innocenti, Francesco Degli; Tosin, Maurizio; Bonomo, Luca; Mezzanotte, Valeria

    2012-01-01

    In modern intensive agriculture, plastics are used in several applications (i.e. mulch films, drip irrigation tubes, string, clips, pots, etc.). Interest towards applying biodegradable plastics to replace the conventional plastics is promising. Ten monomers, which can be applied in the synthesis of potentially biodegradable polyesters, were tested according to ASTM 5988-96 (standard respirometric test to evaluate aerobic biodegradation in soil by measuring the carbon dioxide evolution): adipic acid, azelaic acid, 1,4-butanediol, 1,2-ethanediol, 1,6-hexanediol, lactic acid, glucose, sebacic acid, succinic acid and terephthalic acid. Eight replicates were carried out for each monomer for 27-45 days. The numerical code AQUASIM was applied to process the CO₂ experimental data in order to estimate values for the parameters describing the different mechanisms occurring to the monomers in soil: i) the first order solubilization kinetic constant, K(sol) (d⁻¹); ii) the first order biodegradation kinetic constant, K(b) (d⁻¹); iii) the lag time in biodegradation, t(lag) (d); and iv) the carbon fraction biodegraded but not transformed into CO₂, Y (-). The following range of values were obtained: [0.006 d⁻¹, 6.9 d⁻¹] for K(sol), [0.1 d⁻¹, 1.2 d⁻¹] for K(b), and [0.32-0.58] for Y; t(lag) was observed for azelaic acid, 1,2-ethanediol, and terephthalic acid, with estimated values between 3.0 e 4.9 d. Copyright © 2011 Elsevier Ltd. All rights reserved.

  6. Biomedical Applications of Biodegradable Polyesters

    Directory of Open Access Journals (Sweden)

    Iman Manavitehrani

    2016-01-01

    Full Text Available The focus in the field of biomedical engineering has shifted in recent years to biodegradable polymers and, in particular, polyesters. Dozens of polyester-based medical devices are commercially available, and every year more are introduced to the market. The mechanical performance and wide range of biodegradation properties of this class of polymers allow for high degrees of selectivity for targeted clinical applications. Recent research endeavors to expand the application of polymers have been driven by a need to target the general hydrophobic nature of polyesters and their limited cell motif sites. This review provides a comprehensive investigation into advanced strategies to modify polyesters and their clinical potential for future biomedical applications.

  7. Polyester based hybrid organic coatings

    Science.gov (United States)

    Wang, Xiaojiang

    Polyesters are a class of polymers widely used in organic coatings applications. In this work, four types of organic coatings based on polyester polyols were prepared: UV-curable polyester/poly(meth)acrylate coatings, thermal curable polyester polyurethane-urea coatings, thermal curable non-isocyanate polyurethane coatings, and UV-curable non-isocyanate polyurethane coatings. Polyester/poly(meth)acrylate block copolymers are synthesized using a combination of polycondensation and Atom-Transfer Radical Polymerization (ATRP). All block copolymers are characterized by means of Nuclear Magnetic Resonance (NMR) and Gel Permeation Chromatography (GPC). In the case of unsaturated-polyester-based block copolymers the main chain double bond in the polyester backbone remains almost unaffected during ATRP. The unsaturated block copolymers are crosslinkable and can form networks upon photo-irradiation in the presence of a suitable photoinitiator. These copolymers might be interesting candidates for coatings with better overall properties than those based on neat polyesters. Thermal curable polyester polyol based Polyurethane-Urea (PUU) coatings were formulated using Partially Blocked HDI isocyanurate (PBH), Isophorone Diamine (IPDA), and polyester polyol. As a comparison, the polyurethane coatings (PU) without adding IPDA were also prepared. The mechanical and viscoelastic properties of the PUU and PU coating were investigated by using tensile test and Dynamic Mechanical Thermal Analyzer (DMTA). It was found that PUU coating exhibited higher crosslink density, Tg, tensile modulus and strength than the corresponding PU coating. Thermal curable non-isocyanate polyurethane coatings were prepared by using polyamine and cyclic carbonate terminated polyester. Cyclic carbonate terminated polyester was synthesized from the reaction of the carbon dioxide and epoxidized polyester which was prepared from the polyester polyol. The properties of the epoxidized and cyclic carbonate

  8. Biomedical Applications of Biodegradable Polyesters

    OpenAIRE

    Iman Manavitehrani; Ali Fathi; Hesham Badr; Sean Daly; Ali Negahi Shirazi; Fariba Dehghani

    2016-01-01

    The focus in the field of biomedical engineering has shifted in recent years to biodegradable polymers and, in particular, polyesters. Dozens of polyester-based medical devices are commercially available, and every year more are introduced to the market. The mechanical performance and wide range of biodegradation properties of this class of polymers allow for high degrees of selectivity for targeted clinical applications. Recent research endeavors to expand the application of polymers have be...

  9. The Use of Commercial Non-Hazardous Air Pollutant Monomers to Optimize the Properties of Fatty Acid-Based Resins

    Science.gov (United States)

    2009-05-01

    Reviewing all of the data, it was found that the di-functional monomers produced resins with lower viscosities, higher modulus, and higher Tg than the...to storage modulus Tg Glass transition temperature of polymer TGA Thermogravimetric analysis UPE Unsaturated polyester VE Vinyl ester...The Use of Commercial Non-Hazardous Air Pollutant Monomers to Optimize the Properties of Fatty Acid-Based Resins by John J. La Scala, Priya

  10. Solid-State [2+2] Photodimerization and Photopolymerization of α,ω-Diarylpolyene Monomers: Effective Utilization of Noncovalent Intermolecular Interactions in Crystals

    Directory of Open Access Journals (Sweden)

    Yoriko Sonoda

    2010-12-01

    Full Text Available [2+2] Photocycloaddition of olefins is a very useful reaction in synthetic organic chemistry to obtain cyclobutane-containing molecules, which are almost inaccessible by other methods. The reaction, when performed in the crystalline state, occurs more efficiently and selectively than in homogeneous solution due to tight and regular molecular arrangement in the crystal state. Despite numerous examples for the solid-state [2+2] photodimerization of monoenes, however, it is still a challenge to prepare not only dimers but also higher oligomers and polymers from conjugated polyenes, which have multiple reactive double bonds in a molecule. In our recent studies of the solid-state photoreactions of α,ω-diarylpolyenes, noncovalent intermolecular interactions in crystals were effectively utilized to prealign molecules in stacking arrangements, suitable for the [2+2] reaction. With appropriate ring-substituents, [2+2] photodimerization and photopolymerization of the polyenes took place, although the degree of polymerization was relatively low. This review will describe the details of these reactions.

  11. 液相增黏再生聚酯非等温结晶动力学研究%Non-isothermal crystallization kinetic study of recycled polyester by liquid phase tackifying

    Institute of Scientific and Technical Information of China (English)

    秦丹; 高旭东; 王朝生; 王华平

    2016-01-01

    Post-consumer polyester (PET) fabrics were subjected to friction forming into friction material and were produced in-to blend friction material through screw melting extrusion .The blend friction material was subjected to liquid phase tackifying to produce recycled PET ( R-PET) with a vertical and horizontal double kettle series system .Thus, the recycling utilization of post-consumer PET fabrics was realized .The non-isothermal crystallization kinetics of R-PET was studied and compared with that of traditional PET chips by differential scanning calorimetry ( DSC) .The results showed that the intrinsic viscosity of R-PET was in-creased from 0.580-0.595 dL/g to 0.635-0.655 dL/g after tackification;R-PET had the higher crystalline peak temperatures and shorter semicrystalline time than traditional PET chips at the same cooling rate;and Mo method could well describe the non-isothermal crystallization process of R-PET and traditional PET chips .%将废旧聚酯( PET)纺织品摩擦成形制成摩擦料,再经螺杆熔融挤出制得其共混摩擦料,然后采用立卧双釜串联系统对共混摩擦料进行液相增黏制得再生PET( R-PET),实现废旧PET纺织品的再生利用;利用差示扫描量热( DSC)对 R-PET 进行非等温结晶动力学研究,并与常规 PET 切片进行比较。结果表明:R-PET的特性黏数由未增黏前的0.580~0.595 dL/g增加至0.635~0.655 dL/g;DSC分析中,在同一降温速率下,R-PET的结晶峰温度高于常规PET切片,半结晶时间小于常规PET切片;利用 Mo法可以较好地描述R-PET及常规PET切片的非等温结晶过程。

  12. Reduced toxicity polyester resins and microvascular pre-preg tapes for advanced composites manufacturing

    Science.gov (United States)

    Poillucci, Richard

    Advanced composites manufacturing broadly encapsulates topics ranging from matrix chemistries to automated machines that lay-up fiber-reinforced materials. Environmental regulations are stimulating research to reduce matrix resin formulation toxicity. At present, composites fabricated with polyester resins expose workers to the risk of contact with and inhalation of styrene monomer, which is a potential carcinogen, neurotoxin, and respiratory irritant. The first primary goal of this thesis is to reduce the toxicity associated with polyester resins by: (1) identification of potential monomers to replace styrene, (2) determination of monomer solubility within the polyester, and (3) investigation of approaches to rapidly screen a large resin composition parameter space. Monomers are identified based on their ability to react with polyester and their toxicity as determined by the Globally Harmonized System (GHS) and a green screen method. Solubilities were determined by the Hoftyzer -- Van Krevelen method, Hansen solubility parameter database, and experimental mixing of monomers. A combinatorial microfluidic mixing device is designed and tested to obtain distinct resin compositions from two input chemistries. The push for safer materials is complemented by a thrust for multifunctional composites. The second primary goal of this thesis is to design and implement the manufacture of sacrificial fiber materials suitable for use in automated fiber placement of microvascaular multifunctional composites. Two key advancements are required to achieve this goal: (1) development of a roll-to-roll method to place sacrificial fibers onto carbon fiber pre-preg tape; and (2) demonstration of feasible manufacture of microvascular carbon fiber plates with automated fiber placement. An automated method for placing sacrificial fibers onto carbon fiber tapes is designed and a prototype implemented. Carbon fiber tows with manual placement of sacrificial fibers is implemented within an

  13. The Plant Polyester Cutin: Biosynthesis, Structure, and Biological Roles.

    Science.gov (United States)

    Fich, Eric A; Segerson, Nicholas A; Rose, Jocelyn K C

    2016-04-29

    Cutin, a polyester composed mostly of oxygenated fatty acids, serves as the framework of the plant cuticle. The same types of cutin monomers occur across most plant lineages, although some evolutionary trends are evident. Additionally, cutins from some species have monomer profiles that are characteristic of the related polymer suberin. Compositional differences likely have profound structural consequences, but little is known about cutin's molecular organization and architectural heterogeneity. Its biological importance is suggested by the wide variety of associated mutants and gene-silencing lines that show a disruption of cuticular integrity, giving rise to numerous physiological and developmental abnormalities. Mapping and characterization of these mutants, along with suppression of gene paralogs through RNA interference, have revealed much of the biosynthetic pathway and several regulatory factors; however, the mechanisms of cutin polymerization and its interactions with other cuticle and cell wall components are only now beginning to be resolved.

  14. Enzymatic Synthesis of Biobased Polyesters Using 2,5-Bis(hydroxymethyl)furan as the Building Block

    NARCIS (Netherlands)

    Jiang, Yi; Woortman, Albert J. J.; Alberda van Ekenstein, Gerhard; Petrovic, Dejan M.; Loos, Katja

    2,5-Bis(hydroxymethyl)furan is a highly valuable biobased rigid diol resembling aromatic monomers in polyester synthesis. In this work, it was enzymatically polymerized with various diacid ethyl esters by Candida antarctica Lipase B (CALB) via a three-stage method. A series of novel biobased furan

  15. Degradation of Polyester Polyurethane by Bacterial Polyester Hydrolases

    Directory of Open Access Journals (Sweden)

    Juliane Schmidt

    2017-02-01

    Full Text Available Polyurethanes (PU are widely used synthetic polymers. The growing amount of PU used industrially has resulted in a worldwide increase of plastic wastes. The related environmental pollution as well as the limited availability of the raw materials based on petrochemicals requires novel solutions for their efficient degradation and recycling. The degradation of the polyester PU Impranil DLN by the polyester hydrolases LC cutinase (LCC, TfCut2, Tcur1278 and Tcur0390 was analyzed using a turbidimetric assay. The highest hydrolysis rates were obtained with TfCut2 and Tcur0390. TfCut2 also showed a significantly higher substrate affinity for Impranil DLN than the other three enzymes, indicated by a higher adsorption constant K. Significant weight losses of the solid thermoplastic polyester PU (TPU Elastollan B85A-10 and C85A-10 were detected as a result of the enzymatic degradation by all four polyester hydrolases. Within a reaction time of 200 h at 70 °C, LCC caused weight losses of up to 4.9% and 4.1% of Elastollan B85A-10 and C85A-10, respectively. Gel permeation chromatography confirmed a preferential degradation of the larger polymer chains. Scanning electron microscopy revealed cracks at the surface of the TPU cubes as a result of enzymatic surface erosion. Analysis by Fourier transform infrared spectroscopy indicated that the observed weight losses were a result of the cleavage of ester bonds of the polyester TPU.

  16. 1D zigzag chain and 0D monomer Cd(II)/Zn(II) compounds based on flexible phenylenediacetic ligand: Synthesis, crystal structures and fluorescent properties

    Science.gov (United States)

    Yang, Fang; Ren, Yixia; Li, Dongsheng; Fu, Feng; Qi, Guangcai; Wang, Yaoyu

    2008-12-01

    Three novel Cd(II)/Zn(II) compounds, [Cd 2(poda) 2(phen) 3(H 2O)] n· nEtOH·3 nH 2O (1), [Zn(poda) 2(bpy)(H 2O)] n(2) and [Zn(Hpoda) 2(bpy)] (3) (H 2poda = 1,2-phenylenediacetic acid, phen = 1,10-phenanthroline, bpy = 2,2'-bipyridyl), have been synthesized and characterized by IR, TG, fluorescent spectrum and single-crystal X-ray diffraction techniques. In 1, poda 2- anions link the adjacent Cd(II) centers to generate a 1D zigzag chain. Furthermore, an unprecedented four-footed "8-shaped" mixed water-ethanol (H 2O) 6(C 2H 5OH) 2 cluster connects four double chains based on 1D zigzag chain into 3D supramolecular architecture. By bis(chelate-monodentate) fashion of poda 2- ligand, compound 2 exhibits 1D zigzag chains, which forming a dense zipper-like 2D structure via strong π-π stacking interactions. Differed from 1 and 2, compound 3 has a mononuclear motif, and displays a 3D 6-connected α-Po net hydrogen-bonded topology. The structure-related solid-state fluorescence spectra of compounds 1 and 2 have been determined.

  17. Proton-transfer polymerization (HTP): converting methacrylates to polyesters by an N-heterocyclic carbene.

    Science.gov (United States)

    Hong, Miao; Chen, Eugene Y-X

    2014-10-27

    A new polymerization termed proton (H)-transfer polymerization (HTP) has been developed to convert dimethacrylates to unsaturated polyesters. HTP is catalyzed by a selective N-heterocyclic carbene capable of promoting intermolecular Umpolung condensation through proton transfer and proceeds through the step-growth propagation cycles via enamine intermediates. The role of the added suitable phenol, which is critical for achieving an effective HTP, is twofold: shutting down the radically induced chain-growth addition polymerization under HTP conditions (typically at 80-120 °C) and facilitating proton transfer after each monomer enchainment. The resulting unsaturated polyesters have a high thermal stability and can be readily cross-linked to robust polyester materials. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. 40 CFR 721.9507 - Polyester silane.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Polyester silane. 721.9507 Section 721... Polyester silane. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as a polyester silane (P-95-1022) is subject to reporting under this section for...

  19. Intrinsically microporous polyesters from betulin - toward renewable materials for gas separation made from birch bark.

    Science.gov (United States)

    Jeromenok, Jekaterina; Böhlmann, Winfried; Antonietti, Markus; Weber, Jens

    2011-11-15

    Betulin, an abundant triterpene, can be extracted from birch bark and can be used as a renewable monomer in the synthesis of microporous polyesters. Cross-linked networks and hyperbranched polymers are accessible by an A(2) + B(3) reaction, with betulin being the A(2) monomer and B(3) being a trifunctional acid chloride. Reaction of betulin with a diacid dichloride results in linear, soluble polyesters. The present communication proves that the polyreaction follows the classic schemes of polycondensation reactions. The resulting polymers are analyzed with regard to their micro-porosity by gas sorption, NMR spectroscopy, and X-ray scattering methods. The polymers feature intrinsic microporosity, having ultrasmall pores, which makes them candidates for gas separation membranes, e.g., for the separation of CO(2) from N(2) .

  20. Going greener: Synthesis of fully biobased unsaturated polyesters for styrene crosslinked resins with enhanced thermomechanical properties

    Directory of Open Access Journals (Sweden)

    C. S. M. F. Costa

    2017-11-01

    Full Text Available The main goal of this work was the development of fully biobased unsaturated polyesters (UPs that upon crosslinking with unsaturated monomers (UM could lead to greener unsaturated polyester resins (UPRs with similar thermomechanical properties to commercial fossil based UPR. After the successful synthesis of the biobased UPs, those were crosslinked with styrene (Sty, the most commonly used monomer, and the influence of the chemical structure of the UPs on the thermomechanical characteristics of UPRs were evaluated. The properties were compared with those of a commercial resin (Resipur 9837©. The BioUPRs presented high gel contents and contact angles that are similar to the commercial resin. The thermomechanical properties were evaluated by dynamic mechanical thermal analysis (DMTA and it was found that the UPR synthesized using propylene glycol (PG, succinic acid (SuAc and itaconic acid (ItAc presented very close thermomechanical properties compared to the commercial resin.

  1. PEGylated polyester-based nanoncologicals.

    Science.gov (United States)

    Conte, Claudia; d'Angelo, Ivana; Miro, Agnese; Ungaro, Francesca; Quaglia, Fabiana

    2014-01-01

    Several PEGylated polyester-based nanoncologicals have been proposed in the literature, some of them nowadays being under preclinical/clinical trials or marketed. In this review, we describe the main features of PEGylated polyesters and their correspondent nanocarriers. A first part is devoted to intravenously injectable PEGylated nanocarriers, which represent the systems most investigated so far. After describing fundamental design rules dictated by the administration route, PEGylated nanocarriers currently under preclinical/clinical investigation or in the market will be described from a technological point of view and related therapeutic implications discussed. Finally, new perspective of use of PEGylated nanocarriers for oral and pulmonary delivery of anticancer drugs will be considered.

  2. Rapid Synthesis of a Lipocationic Polyester Library via Ring-Opening Polymerization of Functional Valerolactones for Efficacious siRNA Delivery.

    Science.gov (United States)

    Hao, Jing; Kos, Petra; Zhou, Kejin; Miller, Jason B; Xue, Lian; Yan, Yunfeng; Xiong, Hu; Elkassih, Sussana; Siegwart, Daniel J

    2015-07-29

    The ability to control chemical functionality is an exciting feature of modern polymer science that enables precise design of drug delivery systems. Ring-opening polymerization of functional monomers has emerged as a versatile method to prepare clinically translatable degradable polyesters.1 A variety of functional groups have been introduced into lactones; however, the direct polymerization of tertiary amine functionalized cyclic esters has remained elusive. We report a strategy that enabled the rapid synthesis of >130 lipocationic polyesters directly from functional monomers without protecting groups. These polymers are highly effective for siRNA delivery at low doses in vitro and in vivo.

  3. Renewable Aliphatic Polyester Block Polymer Thermoplastic Elastomers

    Science.gov (United States)

    Martello, Mark Thomas

    The performance of thermoplastic elastomers is predicated on their ability to form mechanically tough physically crosslinked elastomeric networks at low temperatures and be able to flow at elevated temperatures. This dissertation focuses on renewable aliphatic polyester block polymers with amorphous polylactide (PLA) and their performance as TPEs. The goal of this work was to enhance the mechanical toughness of PLA containing TPEs; fundamental properties ranging from chemical composition and phase behavior, molecular architecture and melt processability, to melt polymerization strategies were investigated. ABA triblock polymers with PLA end-blocks and rubbery mid-blocks from substituted lactones comprised of poly(6-methyl-epsilon-caprolactone)(PMCL), poly(delta-decalactone), and poly(epsilon-decalactone)(PDL) were produced by sequential ring-opening polymerizations in the bulk. The bulk microstructure of symmetric PLA-PMCL-PLA and PLA-PDL-PLA triblock polymers formed long-range ordered morphologies and the interaction parameter of the repeat units was determined. High molar mass triblocks exhibited elastomeric behavior with good tensile strengths and high elongations. Small triblocks were coupled to produced (PLA-PDL-PLA)n multiblock polymers with high molar mass and accessible order-disorder transitions allowing for melt processing via injection molding. The mechanical toughness of the multiblocks was comparable to the high molar mass triblocks. The controlled polymerization of renewable delta-decalactone was accomplished with an organocatalyst at low temperatures in the bulk to maximize the equilibrium conversion of the monomer.

  4. Recent developments and future prospects on bio-based polyesters derived from renewable resources: A review.

    Science.gov (United States)

    Zia, Khalid Mahmood; Noreen, Aqdas; Zuber, Mohammad; Tabasum, Shazia; Mujahid, Mohammad

    2016-01-01

    A significantly growing interest is to design a new strategy for development of bio-polyesters from renewable resources due to limited fossil fuel reserves, rise of petrochemicals price and emission of green house gasses. Therefore, this review aims to present an overview on synthesis of biocompatible, biodegradable and cost effective polyesters from biomass and their prospective in different fields including packaging, coating, tissue engineering, drug delivery system and many more. Isosorbide, 2,4:3,5-di-O-methylene-d-mannitol, bicyclic diacetalyzed galactaric acid, 2,5-furandicarboxylic acid, citric, 2,3-O-methylene l-threitol, dimethyl 2,3-O-methylene l-threarate, betulin, dihydrocarvone, decalactone, pimaric acid, ricinoleic acid and sebacic acid, are some important monomers derived from biomass which are used for bio-based polyester manufacturing, consequently, replacing the petrochemical based polyesters. The last part of this review highlights some recent advances in polyester blends and composites in order to improve their properties for exceptional biomedical applications i.e. skin tissue engineering, guided bone regeneration, bone healing process, wound healing and wound acceleration. Copyright © 2015 Elsevier B.V. All rights reserved.

  5. A fast degrading odd-odd aliphatic polyester-5,7 made by condensation polymerization for biomedical applications.

    Science.gov (United States)

    Chen, Fei; Nölle, Jan Martin; Wietzke, Steffen; Reuter, Marco; Chatterjee, Sangam; Koch, Martin; Agarwal, Seema

    2012-01-01

    A fast enzymatic degradable aliphatic all-odd-polyester-5,7, based on 1,7-heptanedioic acid (pimelic acid) and 1,5-pentanediol, was synthesized by polycondensation. The structural characterization of the polyester was done using 1D- and 2D-NMR spectroscopic techniques. The properties of the resulting polyester-like crystallization behavior, enzymatic degradation, thermal stability, etc., were investigated using differential scanning calorimetry, wide-angle X-ray diffraction, scanning electron microscopy and gel-permeation chromatography. Terahertz time-domain spectroscopy was employed to determine the glass transition temperature, which could not be revealed reliably by conventional thermal analysis. The properties of all-odd-polyester-5,7 were compared with a well-known enzymatic degradable polyester (polycaprolactone). The results indicated that polyester-5,7 has a crystal structure similar to PCL, but a much faster degradation rate. The morphology of polyester-5,7 film during enzymatic degradation showed a fibrillar structure and degradation began by surface erosion.

  6. 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.

  7. Bacterial contamination of nurses' white coats made from polyester and polyester cotton blend fabrics.

    Science.gov (United States)

    Gupta, P; Bairagi, N; Priyadarshini, R; Singh, A; Chauhan, D; Gupta, D

    2016-09-01

    In India, nurses wear white coats over their uniform. In this small study, patches of polyester and polyester cotton blend fabrics were attached to the white coats of nurses and sampled for contamination after one shift. Results showed that microbial adhesion is influenced by fabric type, with the microbial load on the polyester cotton blend fabric being 60% higher than that on the polyester fabric. Further studies need to be conducted to establish the correlation between fabric properties and microbial contamination.

  8. Properties of honeycomb polyester knitted fabrics

    Science.gov (United States)

    Feng, A. F.

    2016-07-01

    The properties of honeycomb polyester weft-knitted fabrics were studied to understand their advantages. Seven honeycomb polyester weft-knitted fabrics and one common polyester weft-knitted fabric were selected for testing. Their bursting strengths, fuzzing and pilling, air permeability, abrasion resistance and moisture absorption and perspiration were studied. The results show that the honeycomb polyester weft-knitted fabrics have excellent moisture absorption and liberation. The smaller their thicknesses and area densities are, the better their moisture absorption and liberation will be. Their anti-fuzzing and anti-pilling is good, whereas their bursting strengths and abrasion resistance are poorer compared with common polyester fabric's. In order to improve the hygroscopic properties of the fabrics, the proportion of the honeycomb microporous structure modified polyester in the fabrics should not be less than 40%.

  9. Monomers of cutin biopolymer: sorption and esterification on montmorillonite surfaces

    Science.gov (United States)

    Olshansky, Yaniv; Polubesova, Tamara; Chefetz, Benny

    2013-04-01

    One of the important precursors for soil organic matter is plant cuticle, a thin layer of predominantly lipids that cover all primary aerial surfaces of vascular plants. In most plant species cutin biopolymer is the major component of the cuticle (30-85% weight). Therefore cutin is the third most abundant plant biopolymer (after lignin and cellulose). Cutin is an insoluble, high molecular weight bio-polyester, which is constructed of inter-esterified cross linked hydroxy-fatty acids and hydroxyepoxy-fatty acids. The most common building blocks of the cutin are derivatives of palmitic acid, among them 9(10),16 dihydroxy palmitic acid (diHPA) is the main component. These fatty acids and their esters are commonly found in major organo-mineral soil fraction-humin. Hence, the complexes of cutin monomers with minerals may serve as model of humin. Both cutin and humin act as adsorption efficient domains for organic contaminants. However, only scarce information is available about the interactions of cutin with soil mineral surfaces, in particular with common soil mineral montmorillonite. The main hypothesize of the study is that adsorbed cutin monomers will be reconstituted on montmorillonite surface due to esterification and oligomerization, and that interactions of cutin monomers with montmorillonite will be affected by the type of exchangeable cation. Cutin monomers were obtained from the fruits of tomato (Lycopersicon esculentum). Adsorption of monomers was measured for crude Wyoming montmorillonites and montmorillonites saturated with Fe3+ and Ca2+. To understand the mechanism of monomer-clay interactions and to evaluate esterification on the clay surface, XRD and FTIR analyses of the montmorillonite-monomers complexes were performed. Our results demonstrated that the interactions of cutin monomers with montmorillonite are affected by the type of exchangeable cation. Isotherms of adsorption of cutin monomers on montmorillonites were fitted by a dual mode model of

  10. some tensile properties of unsaturated polyester resin reinforced wi

    African Journals Online (AJOL)

    Dr Obe

    This study investigated the tensile response of polyester composites ... SOME TENSILE PROPERTIES OF UNSATURATED POLYESTER RESIN REINFORCED WITH VARYING VOLUME ... the characterization of the particles and their.

  11. Aza‐Michael addition reaction: Post‐polymerization modification and preparation of PEI/PEG‐based polyester hydrogels from enzymatically synthesized reactive polymers

    DEFF Research Database (Denmark)

    Hoffmann, Christian; Stuparu, Mihaiela C.; Daugaard, Anders Egede

    2015-01-01

    monomers provides the polyesters, which carry an activated carbon‐carbon double bond in the polymer backbone. These electron deficient alkenes represent suitable aza‐Michael acceptors and can be engaged in a nucleophilic addition reaction with small molecular mono‐amines (aza‐Michael donors) to yield...

  12. Biodegradable polyesters based on succinic acid

    Directory of Open Access Journals (Sweden)

    Nikolić Marija S.

    2003-01-01

    Full Text Available Two series of aliphatic polyesters based on succinic acid were synthesized by copolymerization with adipic acid for the first series of saturated polyesters, and with fumaric acid for the second series. Polyesters were prepared starting from the corresponding dimethyl esters and 1,4-butanediol by melt transesterification in the presence of a highly effective catalyst tetra-n-butyl-titanate, Ti(0Bu4. The molecular structure and composition of the copolyesters was determined by 1H NMR spectroscopy. The effect of copolymer composition on the physical and thermal properties of these random polyesters were investigated using differential scanning calorimetry. The degree of crystallinity was determined by DSC and wide angle X-ray. The degrees of crystallinity of the saturated and unsaturated copolyesters were generally reduced with respect to poly(butylene succinate, PBS. The melting temperatures of the saturated polyesters were lower, while the melting temperatures of the unsaturated copolyesters were higher than the melting temperature of PBS. The biodegradability of the polyesters was investigated by enzymatic degradation tests. The enzymatic degradation tests were performed in a buffer solution with Candida cylindracea lipase and for the unsaturated polyesters with Rhizopus arrhizus lipase. The extent of biodegradation was quantified as the weight loss of polyester films. Also the surface of the polyester films after degradation was observed using optical microscopy. It could be concluded that the biodegradability depended strongly on the degree of crystallinity, but also on the flexibility of the chain backbone. The highest biodegradation was observed for copolyesters containing 50 mol.% of adipic acid units, and in the series of unsaturated polyesters for copolyesters containing 5 and 10 mol.% of fumarate units. Although the degree of crystallinity of the unsaturated polyesters decreased slightly with increasing unsaturation, the biodegradation

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

    DEFF Research Database (Denmark)

    Sanchez, C; Alcala, R; Hvilsted, Søren

    2003-01-01

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

  14. Ionic Liquid Epoxy Resin Monomers

    Science.gov (United States)

    Paley, Mark S. (Inventor)

    2013-01-01

    Ionic liquid epoxide monomers capable of reacting with cross-linking agents to form polymers with high tensile and adhesive strengths. Ionic liquid epoxide monomers comprising at least one bis(glycidyl) N-substituted nitrogen heterocyclic cation are made from nitrogen heterocycles corresponding to the bis(glycidyl) N-substituted nitrogen heterocyclic cations by a method involving a non-nucleophilic anion, an alkali metal cation, epichlorohydrin, and a strong base.

  15. Synthesis and Characterization of Branched Poly(ester urea)s with Different Branch Density

    Science.gov (United States)

    Yu, Jiayi; Becker, Matthew

    2015-03-01

    A new class of L-phenylalanine-based poly(ester urea)s (PEU) was developed that possess tunable mechanical properties, water uptake ability and degradation rates. Our preliminary data has shown that 1,6-hexanediol L - phenylalanine-based poly(ester urea)s possesses an elastic modulus nearly double that of poly(lactic acid). My work details the synthesis of a series of L - phenylalanine-based poly(ester urea)s possessing a variation in diol chain length and in branch density and shows how these subtle structural differences influence the mechanical properties and in vitro biodegradation rates. The elastic moduli span a range of values that overlap with several currently clinically available degradable polymers. Increasingly the diol chain lengths increases the amount of flexible segment in the chemical structure, which results in reduced elastic modulus values and increased values of elongation at break. Increasing the amount of branch monomer incorporated into the system reduces the molecular entanglement, which also results in decreased elastic modulus values and increased values of elongation at break. The L - phenylalanine-based poly(ester urea)s also exhibited a diol length dependent degradation process that varied between 1-5 % over 16 weeks. Compared with PLLA, PEUs degrade more quickly and the rate can be tuned by changing the diol chain length. PEUs absorb more water and the water uptake ability can be tuned by changing the branch density. This work was supported by Akron Functional Materials Center.

  16. Analysis of adhesion of radiation curable compositions to polyester substrate. [. gamma. rays or electrons

    Energy Technology Data Exchange (ETDEWEB)

    Walsh, W.K.; Barbery, J.; Gupta, B.S.

    1977-07-01

    Properties of bonds produced by radiation curing of adhesives on polyester film were studied. Investigation of bonding in polyester non-wovens had revealed that adhesion of binders to fibers was weak, which resulted in interfacial failures, judged from electron micrographs. If a binder droplet surrounds a cluster of fibers, tearing of binder took place but fibers still peeled out of droplets with interfacial separation. In order to understand the failure mechanism, a study was carried out on Mylar film bonded with adhesives cured by electron beam or gamma-rays from /sup 60/Co. Mixtures of isodecyl acrylate and methyl methacrylate were copolymerized between Mylar films to produce adhesives with a wide range of glass transition temperatures. Hexanediol diacrylate was added in various amounts to produce different degrees of cross-linking. Small amounts of fumed silica (Cab-O-Sil) were added to thicken the monomers used in the /sup 60/Co experiments. By varying rheological properties in this fashion, a maximum peel force of 3.5 lb/in. was obtained. This value is in line with peel strengths from polyester using commercial, prepolymerized adhesives with solubility parameters similar to those used here delta = 8.3 to 9.3). These results show that the primary reason for the poor adhesion of radiation curable adhesives to polyester is their high degree of cross-linking and that radiation curable adhesives are not basically different from other types, except in cases where their unique properties could be utilized with advantage.

  17. Enhancing the functionality of biobased polyester coating resins through modification with citric acid.

    Science.gov (United States)

    Noordover, Bart A J; Duchateau, Robbert; van Benthem, Rolf A T M; Ming, Weihua; Koning, Cor E

    2007-12-01

    Citric acid (CA) was evaluated as a functionality-enhancing monomer in biobased polyesters suitable for coating applications. Model reactions of CA with several primary and secondary alcohols and diols, including the 1,4:3,6-dianhydrohexitols, revealed that titanium(IV) n-butoxide catalyzed esterification reactions involving these compounds proceed at relatively low temperatures, often via anhydride intermediates. Interestingly, the facile anhydride formation from CA at temperatures around CA's melting temperature ( T m = 153 degrees C) proved to be crucial in modifying sterically hindered secondary hydroxyl end groups. OH-functional polyesters were reacted with CA in the melt between 150 and 165 degrees C, yielding slightly branched carboxylic acid functional materials with strongly enhanced functionality. The acid/epoxy curing reaction of the acid-functional polymers was simulated with a monofunctional glycidyl ether. Finally, the CA-modified polyesters were applied as coatings, using conventional cross-linking agents. The formulations showed rapid curing, resulting in chemically and mechanically stable coatings. These results demonstrate that citric acid can be applied in a new way, making use of its anhydride formation to functionalize OH-functional polyesters, which is an important new step toward fully biobased coating systems.

  18. RHEOLOGY OF CONCENTRATED SOLUTIONS OF HYPERBRANCHED POLYESTERS

    Science.gov (United States)

    The solution rheology of different generations of hyperbranched polyesters in N-methyl-2- pyrrolidinone (NMP) solvent was examined in this study. The solutions exhibited Newtonian behavior over a wide range of polyester concentrations. Also, the relative viscosities of poly(amido...

  19. Polyester Dendrimers: Smart Carriers for Drug Delivery

    Directory of Open Access Journals (Sweden)

    Jean–d’Amour K. Twibanire

    2014-01-01

    Full Text Available Polyester dendrimers have been shown to be outstanding candidates for biomedical applications. Compared to traditional polymeric drug vehicles, these biodegradable dendrimers show excellent advantages especially as drug delivery systems because they are non-toxic. Here, advances on polyester dendrimers as smart carriers for drug delivery applications have been surveyed. Both covalent and non-covalent incorporation of drugs are discussed.

  20. RHEOLOGY OF CONCENTRATED SOLUTIONS OF HYPERBRANCHED POLYESTERS

    Science.gov (United States)

    The solution rheology of different generations of hyperbranched polyesters in N-methyl-2- pyrrolidinone (NMP) solvent was examined in this study. The solutions exhibited Newtonian behavior over a wide range of polyester concentrations. Also, the relative viscosities of poly(amido...

  1. Derivatives of 10,16-Dihydroxyhexadecanoic Acid Isolated from Tomato (Solanum lycopersicum as Potential Material for Aliphatic Polyesters

    Directory of Open Access Journals (Sweden)

    L. Gerardo Zepeda-Vallejo

    2011-06-01

    Full Text Available The main monomer of tomato cuticle, 10,16-dihydroxyhexadecanoic acid (or 10,16-dihydroxypalmitic acid; 10,16-DHPA, was isolated and used to efficiently synthesize two different monomers (16-hydroxy-10-oxo-hexadecanoic and 7-oxohexa-decanedioic acids in addition to a dimer and linear and branched trimers. These compounds were fully characterized using NMR and MS techniques and could be used as starting materials for the synthesis of a wide range of chemicals and bio-polyesters, particularly the latter due to their physical properties, non-toxicity, and relative abundance among raw materials.

  2. Enzymatic polymerization of bio-based monomers for applications in hydrogels and coatings

    DEFF Research Database (Denmark)

    Hoffmann, Christian; Nguyen, Hiep Dinh; Storgaard, Thomas

    Enzymatic polymerization has been gradually building up during the last 30 years as an alternative to classical polyesterificaiton processes, which permits preparation of polyesters under more benign conditions with high selectivity1. In particular, the high selectivity is an interesting property...... of the enzymatic catalysts that can provide control over polymer structure in functional polymers. Lipase catalyzed polymerizations (specifically CALB) has been applied to prepare functional polyesters and to evaluate the possibilities of using less stable bio-based monomers such as itaconic acid or its...... on PEG have been prepared and functionalized through aza-michael additions as well as through thiol-ene chemistry2. Thereby the enzymatically prepared polymer backbone can be considered a scaffold for functional water soluble materials. Finally, these polymers have been applied for preparation...

  3. Monomer Migration and Annihilation Processes

    Institute of Scientific and Technical Information of China (English)

    KE Jian-Hong; LIN Zhen-Quan; ZHUANG You-Yi

    2005-01-01

    We propose a two-species monomer migration-annihilation model, in which monomer migration reactions occur between any two aggregates of the same species and monomer annihilation reactions occur between two different species. Based on the mean-field rate equations, we investigate the evolution behaviors of the processes. For the case with an annihilation rate kernel proportional to the sizes of the reactants, the aggregation size distribution of either species approaches the modified scaling form in the symmetrical initial case, while for the asymmetrical initial case the heavy species with a large initial data scales according to the conventional form and the light one does not scale. Moreover,at most one species can survive finally. For the case with aconstant annihilation rate kernel, both species may scale according to the conventional scaling law in the symmetrical case and survive together at the end.

  4. Iterative tandem catalysis of secondary diols and diesters to chiral polyesters.

    Science.gov (United States)

    van As, Bart A C; van Buijtenen, Jeroen; Mes, Tristan; Palmans, Anja R A; Meijer, E W

    2007-01-01

    The well-known dynamic kinetic resolution of secondary alcohols and esters was extended to secondary diols and diesters to afford chiral polyesters. This process is an example of iterative tandem catalysis (ITC), a polymerization method where the concurrent action of two fundamentally different catalysts is required to achieve chain growth. In order to procure chiral polyesters of high enantiomeric excess value (ee) and good molecular weight, the catalysts employed need to be complementary and compatible during the polymerization reaction. We here show that Shvo's catalyst and Novozym 435 fulfil these requirements. The optimal polymerization conditions of 1,1'-(1,3-phenylene) diethanol (1,3-diol) and diisopropyl adipate required 2 mol% Shvo's catalyst and 12 mg Novozym 435 per mmol alcohol group in the presence of 0.5 M 2,4-dimethyl-3-pentanol as the hydrogen donor. With these conditions, chiral polyesters were obtained with peak molecular weights up to 15 kDa, an ee value up to 99% and with 1-3 % ketone end groups. Also with the structural isomer, 1,4-diol, a chiral polyester was obtained, albeit with lower molecular weight (8.3 kDa) and slightly lower ee (94%). Aliphatic secondary diols also resulted in enantio-enriched polymers but at most an ee of 46 % was obtained with molecular weights in the range of 3.3-3.7 kDa. This low ee originates from the intrinsic low enantioselectivity of Novozym 435 for this type of secondary aliphatic diols. The results presented here show that ITC can be applied to procure chiral polyesters with good molecular weight and high ee from optically inactive AA-BB type monomers.

  5. Castor Oil-Based Biodegradable Polyesters.

    Science.gov (United States)

    Kunduru, Konda Reddy; Basu, Arijit; Haim Zada, Moran; Domb, Abraham J

    2015-09-14

    This Review compiles the synthesis, physical properties, and biomedical applications for the polyesters based on castor oil and ricinoleic acid. Castor oil has been known for its medicinal value since ancient times. It contains ∼90% ricinoleic acid, which enables direct chemical transformation into polyesters without interference of other fatty acids. The presence of ricinoleic acid (hydroxyl containing fatty acid) enables synthesis of various polyester/anhydrides. In addition, castor oil contains a cis-double bond that can be hydrogenated, oxidized, halogenated, and polymerized. Castor oil is obtained pure in large quantities from natural sources; it is safe and biocompatible.

  6. SYNTHESIS, CHARACTERIZATION OF CHIRAL POLY(ESTER AMIDE)S DERIVED FROM L-ISOLEUCINE

    Institute of Scientific and Technical Information of China (English)

    Xing-He Fan; Jing-Lun Zhou; Xiao-Fang Chen; Xin-Hua Wan; Qi-Feng Zhou

    2004-01-01

    A series of new optically active aromatic poly(ester amide)s containing a chiral group in the side chain prepared from the p-toluenesulfonic acid salt of o,o'-bis(leucyl)-hexanediol (TS-+LHD+TS-) and p-phthaloyl chloride and styrene-2,5-dicarbonyl chloride styrene have been synthesized by interfacial polymerization. The structure of the monomer is elucidated by FT-IR and elemental analysis. The thermal properties of the polymers were studied by DSC and TGA. The chiroptical properties of the above polymer have also been studied by circular dichroism (CD) spectroscopy. Results indicated that these polymers form helical structures.

  7. Cyclic polyesters prepared by poly(oxypropylene oxymaloyl ring-chain reactions

    Directory of Open Access Journals (Sweden)

    2007-01-01

    Full Text Available The synthesis of cyclic polyesters of poly(oxypropylene oxymaloyl from a ring-chain reaction was carried out at 40°C with 'Maghnite' an acid exchanged montmorillonite as acid solid ecocatalyst (Mag–H+. 'Maghnite' is already used as catalyst for polymerization of many vinylic and heterocyclic monomers [1]. The effect of amount of catalyst on yield and molecular weight of polymer was studied.A typical reaction product was analyzed by gel permeation chromatography (GPC as well as by nuclear magnetic resonance spectroscopy (1H-NMR and the existence of cyclic species was proven.

  8. Influence of Cobalte Octoate on Degree of Cure and Flexural Strength of an Unsaturated Polyester Resin

    Institute of Scientific and Technical Information of China (English)

    R; M; Gengan; K; Moodley

    2007-01-01

    1 Introduction In the GRP (Glass fibre Reinforced Product) industry Cobalt Octoate is the promoter of choice for cross-linking unsaturated polyester (UPE) and styrene monomer.UPE's are often prepared to contain a concentration of 0.04%-0.05% of Cobalt ions so that faster cross-linking of the resin is achieved and ultimately faster manufacturing of the GRP component is achieved.These products sometimes fail prematurely after being manufactured and dispatched to the end user.The influence of Cobalt Octoat...

  9. Enzyme-catalyzed synthesis of unsaturated aliphatic polyesters based on green monomers from renewable resources

    NARCIS (Netherlands)

    Jiang, Yi; Woortman, Albert J J; van Ekenstein, Gert O R Alberda; Loos, Katja

    2013-01-01

    Bio-based commercially available succinate, itaconate and 1,4-butanediol are enzymatically co-polymerized in solution via a two-stage method, using Candida antarctica Lipase B (CALB, in immobilized form as Novozyme® 435) as the biocatalyst. The chemical structures of the obtained products,

  10. Base-catalyzed depolymerization of lignin : separation of monomers

    Energy Technology Data Exchange (ETDEWEB)

    Vigneault, A. [Sherbrooke Univ., PQ (Canada). Dept. of Chemical Engineering; Johnson, D.K. [National Renewable Energy Laboratory, Golden, CO (United States); Chornet, E. [Sherbrooke Univ., PQ (Canada). Dept. of Chemical Engineering; National Renewable Energy Laboratory, Golden, CO (United States)

    2007-12-15

    Biofuels produced from residual lignocellulosic biomass range from ethanol to biodiesel. The use of lignin for the production of alternate biofuels and green chemicals has been studied with particular emphasis on the structure of lignin and its oxyaromatic nature. In an effort to fractionate lignocellulosic biomass and valorize specific constitutive fractions, the authors developed a strategy for the separation of 12 added value monomers produced during the hydrolytic base catalyzed depolymerization (BCD) of a Steam Exploded Aspen Lignin. The separation strategy was similar to vanillin purification to obtain pure monomers, but combining more steps after the lignin depolymerization such as acidification, batch liquid-liquid-extraction (LLE), followed by vacuum distillation, liquid chromatography (LC) and crystallization. The purpose was to develop basic data for an industrial size process flow diagram, and to evaluate both the monomer losses during the separation and the energy requirements. Experimentally testing of LLE, vacuum distillation and flash LC in the laboratory showed that batch vacuum distillation produced up to 4 fractions. Process simulation revealed that a series of 4 vacuum distillation columns could produce 5 distinct monomer streams, of which 3 require further chromatography and crystallization operations for purification. 22 refs., 4 tabs., 8 figs.

  11. GENERAL: Cluster Growth Through Monomer Adsorption Processes

    Science.gov (United States)

    Ke, Jian-Hong; Lin, Zhen-Quan; Chen, Xiao-Shuang

    2010-02-01

    We propose a monomer adsorption model, in which only the monomers are allowed to diffuse and adsorb onto other clusters. By means of the generalized rate equation we investigate the kinetic behavior of the system with a special rate kernel. For the system without monomer input, the concentration aj(t) of the Aj clusters (j > 1) asymptotically retains a nonzero quantity, while for the system with monomer input, it decays with time and vanishes finally. We also investigate the kinetics of an interesting model with fixed-rate monomer adsorption. For the case without monomer source, the evolution of the system will halt at a finite time; while the system evolves infinitely in time in the case with monomer source. Finally, we also suggest a connection between the fixed-rate monomer adsorption systems and growing networks.

  12. Hyperbranched polyester: single route synthesis, characterization and evaluation as impact modifier of an epoxy resin; Poliester hiperramificado: sintese por uma rota simples, caracterizacao e avaliacao como modificador de impacto de uma resina epoxi

    Energy Technology Data Exchange (ETDEWEB)

    Miranda, B.H.S.; Sousa, A.R., E-mail: rangel@deii.cefetmg.br [Centro Federal de Educacao Tecnologica de Minas Gerais (DEMAT/CEFET-MG), Belo Horizonte (Brazil). Departamento de Engenharia de Materiais; Alves, A.P.P.; Silva, G.G. [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte (Brazil). Departamento de Quimica. Lab. de Materiais Polimericos Multicomponentes

    2015-07-01

    Two hyperbranched polyesters were obtained using glycerol and adipic acid as monomers, they were characterized through nuclear magnetic resonance ({sup 13}C NMR) to branching degree determination, size exclusion chromatography to molar mass obtention and thermogravimetric analysis (TGA) to evaluate the thermal stability. The polyesters synthesized were added to epoxy resin, at 10% by weight, to evaluate the implication on mechanical properties, impact and stress strain, and thermal (glassy transition temperature - Tg). We observed that rising the synthesis time from 6 to 15,5 hours the degree of branching, molar mass and thermal stability of the polyester increased. The addition of hyperbranched polyesters did not change the mechanical properties of epoxy resin significantly, but the Tg was reduced. (author)

  13. Analytical approaches to identify potential migrants in polyester-polyurethane can coatings.

    Science.gov (United States)

    Louise Bradley, Emma; Driffield, Malcolm; Guthrie, James; Harmer, Nick; Thomas Oldring, Peter Kenneth; Castle, Laurence

    2009-12-01

    The safety of a polyester-polyurethane can coating has been assessed using a suite of complementary analytical methods to identify and estimate the concentrations of potential chemical migrants. The polyester was based on phthalic acids and aliphatic diols. The polyisocyanate cross-linking agent was 1-isocyanato-3-isocyanatomethyl-3,5,5-trimethyl cyclohexane homopolymer (IPDI) blocked with methylethylketone oxime (MEKO) to make a one-part formulation. The overall migrate, obtained using solvent extraction of cured films, comprised almost completely of 12 cyclic and one linear polyester oligomer up to molecular weight 800 and containing up to six monomer units. These 13 oligomers covered a total of 28 isomeric forms. Other minor components detected were plasticisers and surfactants as well as impurities present in the starting materials. There was no detectable residue of either the blocked isocyanate (<0.01 microg/dm(2)) used as the starting substance or the unblocked isocyanate (<0.02 microg/dm(2)). The level of extractable IPDI was used as an indicator of the completeness of cure in experimental coatings. These studies revealed that there was an influence of time, temperature and catalyst content. Polymerisation was also influenced by the additives used and by the ageing of the wet coating formulation over several months. These studies allow parameters to be specified to ensure that commercial production coatings receive a full cure giving low migration characteristics.

  14. Cure characterization of an unsaturated polyester resin using near-infrared, fluorescence and UV/visible reflection spectroscopies

    Science.gov (United States)

    Grunden, Bradley Lyn

    This dissertation seeks to characterize the cure reaction of an unsaturated polyester resin using near-infrared, fluorescence and UV/Visible reflection spectroscopies. The results will provide a foundation for developing fiber-optic in-situ cure monitoring techniques based on near-infrared, fluorescence, and UV/Visible reflection spectroscopies for an unsaturated polyester resin system. Near-infrared spectra of the unsaturated polyester resin during cure showed a decrease in absorption at 1629, 2087, 2117, and 2227 nm. Model compounds representing the reactants and products of the cure reaction were characterized, and assignment of peaks in the NIR were made. Conversion of styrene and vinylene, determined from NIR measurements, were compared with values obtained using conventional FTIR measurements. Discrepancies between conversion values determined from NIR and FTIR measurements were attributed to a difference in sample sizes used for measurement. Using a microgel based reaction mechanism, the effects of temperature on the conversion of styrene and vinylene was discussed. A strong fluorescence emission was found during cure of the unsaturated polyester resin. As the reaction proceeded, the emission intensity at 306 nm increased. Model compound studies confirmed that the unsaturated polyester vinylene component exhibits negligible fluorescence when excited at 250 nm. The fluorescence emission at 306 nm was attributed to a reduced self-quenching effect of styrene monomer. In-situ fluorescence characterization of the cure reaction was also attempted. Fiber-optic fluorescence measurements taken in-situ at 75°C were found to be higher than those taken by fiber-optics at room temperature, indicating a temperature effect on the fluorescence emission. These results may be a consequence of the static quenching behavior of styrene monomer. UV/Visible reflection spectra of styrene showed a decrease in the % Reflectance at 255 nm with reaction time. This decrease was

  15. ADVANCES IN LIQUID CRYSTALLINE POLYESTERS

    Institute of Scientific and Technical Information of China (English)

    W. J. Jackson

    1992-01-01

    Advances have been made in understanding the interactions of composition, molecular weight,liquid crystallinity, orientation, and three-dimensional crystallinity on the properties of injection-molded and melt-spun liquid crystalline polyesters (LCP's). Two classes of potentially low-cost LCP's were compared : (1) semiflexible LCP's prepared from 1,6-hexanediol and the dimethyl ester of either trans-4, 4'-stilbenedicarboxylic acid or 4.4 ′-biphenyldicarboxylic acid and (2) all-aromatic LCP's prepared from terephthalic acid, 2, 6-naphthalenedicarboxylic acid, the diacetate of hydroquinone,and the acetate of p-hydroxybenzoic acid. The effects of composition on the plastic properties of the 4-component all-aromatic LCP's were determined with the aid of a 3 × 3 factorial statistically designed experiment, the generation of equations with a computer program, and the plotting of three-dimensional figures and contour diagrams. The effects of absolute molecular weight (Mw) on the tensile strengths of the semiflexible LCP's and one of the all-aromatic LCP's having an excellent balance of plastic properties were also compared, and it was observed that the semiflexible LCP's required Mw's about 4 times higher than the all-aromatic LCP to attain a given strength. Persistence lengths and molecular modeling were used to explain these differences.

  16. Evaluation of Long-Term Migration Testing from Can Coatings into Food Simulants: Polyester Coatings.

    Science.gov (United States)

    Paseiro-Cerrato, Rafael; Noonan, Gregory O; Begley, Timothy H

    2016-03-23

    FDA guidance for food contact substances recommends that for food packaging intended for use at sterilized, high temperature processed, or retorted conditions, a migration test with a retort step at 121 °C for 2 h followed by a 10 day migration test at 40 °C should be performed. These conditions are in intended to simulate processing and long-term storage. However, can coatings may be in contact with food for years, and there are very few data evaluating if this short-term testing accurately simulates migration over extended time periods. A long-term migration test at 40 °C with retorted and non-retorted polyester cans using several food simulants (water, 3% acetic acid, 10% ethanol, 50% ethanol, and isooctane) was conducted to verify whether traditional migration testing protocols accurately predict migration from food contact materials used for extended time periods. Time points were from 1 day to 515 days. HPLC-MS/MS was used to analyze polyester monomers, and oligomer migration was monitored using HPLC-DAD/CAD and HPLC-MS. Concentrations of monomers and oligomers increased during the migration experiments, especially in ethanol food simulants. The data suggest that current FDA migration protocols may need to be modified to address changes in migrants as a result of long-term storage conditions.

  17. The aliphatic counterpart of PET, PPT and PBT aromatic polyesters: effect of the molecular structure on thermo-mechanical properties

    Directory of Open Access Journals (Sweden)

    Morgane Albanese

    2016-02-01

    Full Text Available The aliphatic counterparts of the most used aromatic polyesters (PET, PPT, and PBT have been synthesized by a two-stage polycondensation process, starting from dimethyl 1,4-cyclohexane dicarboxylate and different diols. The fully aliphatic polyesters are characterized by two cis/trans isomeric ratios (50 and 90 mol% of the 1,4-cycloaliphatic rings. According to the cis/trans content, the properties of the materials notably change. Indeed, polymers rich in trans isomer are semicrystalline, whereas polymers with low trans content are fully amorphous, due to the presence of kinks along the chain. Trans isomer is characterized by higher rigidity than the cis one and the corresponding polymers have high glass transition temperatures. Moreover, the length of the methylene sequences in the diol has a notable influence on the final thermal and mechanical properties. Therefore, tunable properties can be easily obtained. This characteristic, in association with good mechanical performances, potential sustainability of the monomers and biodegradability, makes these aliphatic polyesters an interesting class of polyesters for some specific applications.

  18. 77 FR 60720 - Certain Polyester Staple Fiber From China

    Science.gov (United States)

    2012-10-04

    ... COMMISSION Certain Polyester Staple Fiber From China Determination On the basis of the record \\1\\ developed... antidumping duty order on certain polyester staple fiber from China would be likely to lead to continuation or... USITC Publication 4351 (September 2012), entitled Certain Polyester Staple Fiber from...

  19. Rewritable azobenzene polyester for polarization holographic data storage

    DEFF Research Database (Denmark)

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

    2000-01-01

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

  20. 40 CFR 721.8082 - Polyester polyurethane acrylate.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Polyester polyurethane acrylate. 721... Substances § 721.8082 Polyester polyurethane acrylate. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as polyester polyurethane...

  1. Advanced bacterial polyhydroxyalkanoates: towards a versatile and sustainable platform for unnatural tailor-made polyesters.

    Science.gov (United States)

    Park, Si Jae; Kim, Tae Wan; Kim, Min Kyung; Lee, Sang Yup; Lim, Sung-Chul

    2012-01-01

    Polyhydroxyalkanoates (PHAs) are biopolyesters that generally consist of 3-, 4-, 5-, and 6-hydroxycarboxylic acids, which are accumulated as carbon and energy storage materials in many bacteria in limited growth conditions with excess carbon sources. Due to the diverse substrate specificities of PHA synthases, the key enzymes for PHA biosynthesis, PHAs with different material properties have been synthesized by incorporating different monomer components with differing compositions. Also, engineering PHA synthases using in vitro-directed evolution and site-directed mutagenesis facilitates the synthesis of PHA copolymers with novel material properties by broadening the spectrum of monomers available for PHA biosynthesis. Based on the understanding of metabolism of PHA biosynthesis, recombinant bacteria have been engineered to produce different types of PHAs by expressing heterologous PHA biosynthesis genes, and by creating and enhancing the metabolic pathways to efficiently generate precursors for PHA monomers. Recently, the PHA biosynthesis system has been expanded to produce unnatural biopolyesters containing 2-hydroxyacid monomers such as glycolate, lactate, and 2-hydroxybutyrate by employing natural and engineered PHA synthases. Using this system, polylactic acid (PLA), one of the major commercially-available bioplastics, can be synthesized from renewable resources by direct fermentation of recombinant bacteria. In this review, we discuss recent advances in the development of the PHA biosynthesis system as a platform for tailor-made polyesters with novel material properties. Copyright © 2011 Elsevier Inc. All rights reserved.

  2. Radiopaque, iodine functionalized, phenylalanine-based poly(ester urea)s.

    Science.gov (United States)

    Li, Shan; Yu, Jiayi; Wade, Mary Beth; Policastro, Gina M; Becker, Matthew L

    2015-02-01

    The synthesis and characterization of iodine-functionalized phenylalanine-based poly(ester urea)s (PEUs) are reported. 4-Iodo-L-phenylalanine and L-phenylalanine were separately reacted with 1,6-hexanediol to produce two monomers, bis-4-I-L-phenylalanine-1,6-hexanediol-diester (1-IPHE-6 monomer) and bis-L-phenylalanine-1,6-hexanediol-diester (1-PHE-6 monomer). By varying the feed ratio of the 1-IPHE-6 and 1-PHE-6 monomers, the copolymer composition was modulated resulting in a wide variation in thermal, mechanical and radiopacity properties. Microcomputed tomography (μ-CT) projections demonstrate that increasing iodine content results in greater X-ray contrast. Compression tests of dry and wet porous scaffolds indicate that the poly(1-IPHE-6)0.24-co-poly(1-PHE-6)0.76 material results in the highest compression modulus. MC3T3 cell viability and spreading studies show PEUs are nontoxic to cells. As most medical device procedures require placement verification via fluoroscopic imaging, materials that possess inherent X-ray contrast are valuable for a number of applications.

  3. 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.

  4. Functional polyester fabric through simultaneous aminolysis and nano ZnO synthesis

    Directory of Open Access Journals (Sweden)

    Hajar Poortavasoly

    2014-12-01

    Full Text Available Here, in situ synthesis of nano zinc oxide, along with aminolysis of polyester fabric, has simultaneously been carried out by using triethanol amine (TEA and zinc acetate. The ZnO nano particles (NPs were formed and stabilized on the fabric surface by amine compound at 130 °C for 1 h. The synthesis of nano ZnO particles on the polyester fabric were confirmed by X-ray diffraction (XRD patterns and scanning electron microscopy (SEM images. The mean size of ZnO NP was obtained with SEM about 51.38 nm, however, XRD data indicated the crystalline ZnO NPs with a mean crystal size of 14.68 nm on the fabric surface. Further, self-cleaning performance of the treated fabrics was studied by degradation of methylene blue (MB in aqueous solution under daylight irradiation. The stability of ZnO NPs on the fabric surface was studied by evaluating the self-cleaning and hydrophilicity properties of the samples after standard washing. Also, the hydrophilicity of the treated polyester fabric was improved due to aminolysis of the fabric and the required time for water droplet to spread on the treated fabric after one week exposure to daylight reduced. Overall, TEA was a suitable reducing agent to prepare homogenous ZnO NPs on the polyester fabric.

  5. Biodegradable polyesters reinforced with triclosan loaded polylactide micro/nanofibers: Properties, release and biocompatibility

    Directory of Open Access Journals (Sweden)

    L. J. del Valle

    2012-04-01

    Full Text Available Mechanical properties and drug release behavior were studied for three biodegradable polyester matrices (polycaprolactone, poly(nonamethylene azelate and the copolymer derived from 1,9-nonanediol and an equimolar mixture of azelaic and pimelic acids reinforced with polylactide (PLA fibers. Electrospinning was used to produce suitable mats constituted by fibers of different diameters (i.e. from micro- to nanoscale and a homogeneous dispersion of a representative hydrophobic drug (i.e. triclosan. Fabrics were prepared by a molding process, which allowed cold crystallization of PLA micro/nanofibers and hot crystallization of the polyester matrices. The orientation of PLA molecules during electrospinning favored the crystallization process, which was slightly enhanced when the diameter decreased. Incorporation of PLA micro/nanofibers led to a significant increase in the elastic modulus and tensile strength, and in general to a decrease in the strain at break. The brittle fracture was clearer when high molecular weight samples with high plastic deformation were employed. Large differences in the release behavior were detected depending on the loading process, fiber diameter size and hydrophobicity of the polyester matrix. The release of samples with the drug only loaded into the reinforcing fibers was initially fast and then became slow and sustained, resulting in longer lasting antimicrobial activity. Biocompatibility of all samples studied was demonstrated by adhesion and proliferation assays using HEp-2 cell cultures.

  6. New chemically reworkable epoxy coatings obtained by the addition of polyesters with star topologies to diglycidyl ether of bisphenol A resins

    OpenAIRE

    Tomuta, Adrian Marius; Ramis Juan, Xavier; Fernández Francos, Xavier; Ferrando Piera, Francesc; Serra Albet, Àngels

    2013-01-01

    A new multiarm star with hyperbranched aromatic–aliphatic polyester core and poly(ɛ-caprolactone) arms (HBPCL) was synthesized and characterized. Mixtures of diglycidyl ether of bisphenol A (DGEBA) resin and different proportions of this star type modifier were cured using a thermal cationic curing agent, Yb(OTf)3. The HBPCL prepared has hydroxyl groups as chain ends, which are capable of chemically incorporating to the epoxy matrix by means of the monomer activated mechanism. This, together ...

  7. Properties of Surface Cyclic Oligomers Present on Polyester Fiber

    Institute of Scientific and Technical Information of China (English)

    郑敏; 宋心远

    2003-01-01

    The effects of different treatments, such as dry heat,wet heat, solvent vapor and ultrasonic, on properties of the cyclic oligomers on the surface of polyester fiber are studied. The components of surface oligomers are analyzed through Thin-Layer Chromatograph. The result shows that: all of the treatments, especially solvent vapor treatment, can significantly increase the content of surface cyclic oligomers. The content of cyclic trimer is increased more considerably than other oligomers. Moreover, the morphology and the distribution of surface cyclic oligomers are also different from different treatments: Dry heat and wet heat cause larger polygonal solids distributed evenly on the surface of fiber; solvent vapor makes fiber surface exhibit irregular rodlike crystal shapes randomly; ultrasonic treatment induces some obscure and smaller deposits on the surface of fiber.

  8. UV curable hard coatings on polyesters

    Science.gov (United States)

    Datashvili, Tea; Brostow, Witold; Kao, David

    2006-10-01

    UV curable, hard and transparent hybrid inorganic-organic coatings with covalent links between the inorganic and the organic networks were prepared using organically crosslinked heteropolysiloxanes based on the sol-gel process. The materials were applied onto polyester sheets and UV cured. The deposition was followed by a thermal treatment to improve mechanical properties of the coatings. High light transmission and the resulting thermophysical properties indicate the presence of a nanoscale hybrid composition. The coatings show excellent adhesion to polyesters even without using primers. Further mechanical characterization shows that the coatings provide high hardness and good abrasion resistance.

  9. Synthesis, Properties and Applications of Biodegradable Polymers Derived from Diols and Dicarboxylic Acids: From Polyesters to Poly(ester amides

    Directory of Open Access Journals (Sweden)

    Angélica Díaz

    2014-04-01

    Full Text Available Poly(alkylene dicarboxylates constitute a family of biodegradable polymers with increasing interest for both commodity and speciality applications. Most of these polymers can be prepared from biobased diols and dicarboxylic acids such as 1,4-butanediol, succinic acid and carbohydrates. This review provides a current status report concerning synthesis, biodegradation and applications of a series of polymers that cover a wide range of properties, namely, materials from elastomeric to rigid characteristics that are suitable for applications such as hydrogels, soft tissue engineering, drug delivery systems and liquid crystals. Finally, the incorporation of aromatic units and α-amino acids is considered since stiffness of molecular chains and intermolecular interactions can be drastically changed. In fact, poly(ester amides derived from naturally occurring amino acids offer great possibilities as biodegradable materials for biomedical applications which are also extensively discussed.

  10. Surface active monomers synthesis, properties, and application

    CERN Document Server

    Borzenkov, Mykola

    2014-01-01

    This brief includes information on the background?of and development of synthesis of various types of surface active monomers. The authors explain the importance of utilization of surface active monomers for creation of surface active polymers? and the various biomedical applications of such compounds . This brief introduces techniques for the synthesis of novel types of surface active monomers, their colloidal and polymerizable properties and application for needs of medicine and biology.

  11. Resisting protein adsorption on biodegradable polyester brushes.

    Science.gov (United States)

    Hu, Xinfang; Gorman, Christopher B

    2014-08-01

    The protein adsorption and degradation behaviors of poly(lactic acid), poly(glycolic acid) (PGA) and poly(ε-caprolactone) (PCL) brushes and their co-polymer brushes with oligo(ethylene glycol) (OEG) were studied. Both brush structure and relative amount of OEG and polyester were found to be important to the protein resistance of the brushes. A protein-resisting surface can be fabricated either by using OEG as the top layer of a copolymer brush or by increasing the amount of OEG relative to polyester when using a hydroxyl terminated OEG (OEG-OH) and a methoxy terminated OEG (OEG-OMe) mixture as the substrate layer. The degradation of single polyester brushes and their co-polymer brushes using OEG-OH as a substrate layer or using OEG as a top layer was hindered. This phenomenon was rationalized by the inhibition of the proposed back-biting process as the hydroxy end groups of polyester were blocked by OEG molecules. Among these brushes tested, PGA co-polymer brushes using the methoxy/hydroxyl OEG mixture as the substrate layer proved to be both protein-resistant and degradable due to the relatively large amount of OEG moieties and the good biodegradability of PGA.

  12. Micro-thermal analysis of polyester coatings

    NARCIS (Netherlands)

    Fischer, H.R.

    2010-01-01

    The application and suitability of micro-thermal analysis to detect changes in the chemical and physical properties of coating due to ageing and especially photo-degradation is demonstrated using a model polyester coating based on neopentyl glycol isophthalic acid. The changes in chemical structure

  13. Holographic recording in thiophene-based polyester

    DEFF Research Database (Denmark)

    Matharu, Avtar Singh; Chambers-Asman, David; Jeeva, Shehzad

    2008-01-01

    The synthesis and optical data storage properties of a side-chain thiophene-phenyl azopolyester ThPhAzoP.ol is reported. The polyester is derived from diphenyl tetradecanedioate and a thiophenebased liquid crystalline diol which exhibits a short-lived enantiotropic SmA phase (Cryst 177.7 SmA 180...

  14. Micro-thermal analysis of polyester coatings

    NARCIS (Netherlands)

    Fischer, H.R.

    2010-01-01

    The application and suitability of micro-thermal analysis to detect changes in the chemical and physical properties of coating due to ageing and especially photo-degradation is demonstrated using a model polyester coating based on neopentyl glycol isophthalic acid. The changes in chemical structure

  15. Photoinduced Deformation of Azobenzene Polyester Films

    DEFF Research Database (Denmark)

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

    2000-01-01

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

  16. Carboxylated Polyurethanes Containing Hyperbranched Polyester Soft Segments

    Directory of Open Access Journals (Sweden)

    Žigon, M.

    2006-09-01

    Full Text Available hyperbranched polyester soft segments (HB PU with functional carboxylic groups in order to enable the preparation of stable HB PU dispersions. Carboxylated hyperbranched polyurethanes were synthesized using a hyperbranched polyester based on 2,2-bis(methylolpropionic acid of the fourth pseudo-generation (Boltorn H40 and hexamethylene (HDI or isophorone diisocyanate (IPDI. The reactivity of hyperbranched polyester with HDI was lower than expected, possibly due to the presence of less reactive hydroxyl groups in the linear repeat units. A gel was formed at mole ratios rNCO/OH = 1:2 or 1:4. The synthesis of HB PU was performed with partly esterified hyperbranched polyester with lowered hydroxyl functionality. The carboxyl groups were incorporated in the HB PU backbone by reaction of residual hydroxyl groups with cis-1,2-cyclohexanedicarboxylic anhydride. HB PU aqueous dispersions were stable at least for two months, although their films were brittle. The tensile strength and Young's modulus of blends of linear and HB PU decreased with increasing content of HB PU whereas elongation at break remained nearly constant, which was explained in terms of looser chain packing due to more open tree-like hyperbranched structures.

  17. Correlation spectroscopy applied to glycerol polyester spectra

    Science.gov (United States)

    The recent development of glycerol polyesters for use as controlled release matrix materials in the nutraceuticals and pharmaceuticals industries presented a unique opportunity to apply correlation spectroscopy. In a typical formulation the glycerol is reacted with a polyfunctional acid such as citr...

  18. New poly(ester urea) derived from L-leucine: Electrospun scaffolds loaded with antibacterial drugs and enzymes

    Energy Technology Data Exchange (ETDEWEB)

    Díaz, Angélica; Valle, Luis J. del [Departament d' Enginyeria Química, Universitat Politècnica de Catalunya, Av. Diagonal 647, Barcelona E-08028 (Spain); Tugushi, David; Katsarava, Ramaz [Institute of Chemistry and Molecular Engineering, Agricultural University of Georgia, 13 km. David Aghmashenebeli Alley, Tblisi 0131, Georgia (United States); Puiggalí, Jordi, E-mail: Jordi.Puiggali@upc.edu [Departament d' Enginyeria Química, Universitat Politècnica de Catalunya, Av. Diagonal 647, Barcelona E-08028 (Spain)

    2015-01-01

    Electrospun scaffolds from an amino acid containing poly(ester urea) (PEU) were developed as promising materials in the biomedical field and specifically in tissue engineering applications. The selected poly(ester urea) was obtained with a high yield and molecular weight by reaction of phosgene with a bis(α-aminoacyl)-α,ω-diol-diester monomer. The polymer having L-leucine, 1,6-hexanediol and carbonic acid units had a semicrystalline character and relatively high glass transition and melting temperatures. Furthermore it was highly soluble in most organic solvents, an interesting feature that facilitated the electrospinning process and the effective incorporation of drugs with bactericidal activity (e.g. biguanide derivatives such as clorhexidine and polyhexamethylenebiguanide) and enzymes (e.g. α-chymotrypsin) that accelerated the degradation process. Continuous micro/nanofibers were obtained under a wide range of processing conditions, being diameters of electrospun fibers dependent on the drug and solvent used. Poly(ester urea) samples were degradable in media containing lipases and proteinases but the degradation rate was highly dependent on the surface area, being specifically greater for scaffolds with respect to films. The high hydrophobicity of new scaffolds had repercussions on enzymatic degradability since different weight loss rates were found depending on how samples were exposed to the medium (e.g. forced or non-forced immersion). New scaffolds were biocompatible, as demonstrated by adhesion and proliferation assays performed with fibroblast and epithelial cells. - Highlights: • Electrospun scaffolds from a biodegradable poly(ester urea) have been prepared. • Scaffolds were effectively loaded with bactericide agents. • Enzymatic degradability of the L-leucine derived poly(ester urea) was demonstrated. • Enzymes that accelerate degradation were incorporated in the electrospun fibers. • Cell adhesion/proliferation assays demonstrated

  19. An Esterase from Anaerobic Clostridium hathewayi Can Hydrolyze Aliphatic-Aromatic Polyesters.

    Science.gov (United States)

    Perz, Veronika; Hromic, Altijana; Baumschlager, Armin; Steinkellner, Georg; Pavkov-Keller, Tea; Gruber, Karl; Bleymaier, Klaus; Zitzenbacher, Sabine; Zankel, Armin; Mayrhofer, Claudia; Sinkel, Carsten; Kueper, Ulf; Schlegel, Katharina; Ribitsch, Doris; Guebitz, Georg M

    2016-03-15

    Recently, a variety of biodegradable polymers have been developed as alternatives to recalcitrant materials. Although many studies on polyester biodegradability have focused on aerobic environments, there is much less known on biodegradation of polyesters in natural and artificial anaerobic habitats. Consequently, the potential of anaerobic biogas sludge to hydrolyze the synthetic compostable polyester PBAT (poly(butylene adipate-co-butylene terephthalate) was evaluated in this study. On the basis of reverse-phase high-performance liquid chromatography (RP-HPLC) analysis, accumulation of terephthalic acid (Ta) was observed in all anaerobic batches within the first 14 days. Thereafter, a decline of Ta was observed, which occurred presumably due to consumption by the microbial population. The esterase Chath_Est1 from the anaerobic risk 1 strain Clostridium hathewayi DSM-13479 was found to hydrolyze PBAT. Detailed characterization of this esterase including elucidation of the crystal structure was performed. The crystal structure indicates that Chath_Est1 belongs to the α/β-hydrolases family. This study gives a clear hint that also micro-organisms in anaerobic habitats can degrade manmade PBAT.

  20. Nanoprecipitation and Spectroscopic Characterization of Curcumin-Encapsulated Polyester Nanoparticles.

    Science.gov (United States)

    Leung, Mandy H M; Harada, Takaaki; Dai, Sheng; Kee, Tak W

    2015-10-27

    Curcumin-encapsulated polyester nanoparticles (Cur-polyester NPs) of approximately 100 nm diameter with a negatively charged surface were prepared using a one-step nanoprecipitation method. The Cur-polyester NPs were prepared using polylactic acid, poly(D,L-lactic-co-glycolic acid) and poly(ϵ-caprolactone) without any emulsifier or surfactant. The encapsulation of curcumin in these polyester NPs greatly suppresses curcumin degradation in the aqueous environment due to its segregation from water. In addition, the fluorescence of curcumin in polyester NPs has a quantum yield of 4 to 5%, which is higher than that of curcumin in micellar systems and comparable to those in organic solvents, further supporting the idea that the polyester NPs are capable of excluding water from curcumin. Furthermore, the results from femtosecond fluorescence upconversion spectroscopy reveal that there is a decrease in the signal amplitude corresponding to solvent reorganization of excited state curcumin in the polyester NPs compared with curcumin in micellar systems. The Cur-polyester NPs also show a lack of deuterium isotope effect in the fluorescence lifetime. These results indicate that the interaction between curcumin and water in the polyester NPs is significantly weaker than that in micelles. Therefore, the aqueous stability of curcumin is greatly improved due to highly effective segregation from water. The overall outcome suggests that the polyester NPs prepared using the method reported herein are an attractive system for encapsulating and stabilizing curcumin in the aqueous environment.

  1. Enzymatic Synthesis and Characterization of Hydrophilic Sugar Based Polyesters and Their Modification with Stearic Acid

    Directory of Open Access Journals (Sweden)

    Muhammad Humayun Bilal

    2016-03-01

    Full Text Available Biodegradable and hydrophilic functional polyesters were synthesized enzymatically using xylitol or d-sorbitol together with divinyl adipate and lipase B from Candida antartica (CAL-B. The resulting polyesters had pendant OH-groups from their sugar units which were esterified to different degrees with stearic acid chloride. The structure and the degrees of polymerization of the resulting graft copolymers based on poly(xylitol adipate and poly(d-sorbitol adipate were characterized by 1H NMR spectroscopy and SEC. DSC, WAXS and SAXS measurements indicated that a phase separation between polymer backbone and stearoyl side chains occurred in the graft copolymers, and, additionally, the side chains were able to crystallize which resulted in the formation of a lamellar morphology. Additionally, nanoparticles of the graft copolymers in an aqueous environment were studied by DLS and negative stain TEM.

  2. Synthesis and characterization of poly(ester amide from remewable resources through melt polycondensation

    Directory of Open Access Journals (Sweden)

    B. B. Wang

    2014-01-01

    Full Text Available Biodegradable poly(ester amides (PEAs were synthesized from lactic acid and 11-aminoundecanoic acid via melt polycondensation. Molecular weights, chemical structures and thermal properties of the poly(ester amides were characterized in terms of gel permeation chromatography (GPC, Fourier transform infrared spectroscopy (FTIR, 1H nuclear magnetic resonance (1H NMR, differential scanning calorimetry (DSC and thermogravimetric analysis (TGA, respectively. The PEAs have low molecular weights and display a lower cold crystallization temperature as well as smaller crystallinity by comparison with the pure poly(lactic acid (PLA. The incorporation of the 11-aminoundecanoic acid into the PLA chain not only improved the thermal stability but changed the decomposition process.

  3. Synthesis and characterization of oleophobic fluorinated polyester films

    Science.gov (United States)

    Demir, Tugba

    The study presented in this dissertation is dedicated to the synthesis and characterization of oleophobic fluorinated polyester films. Specifically, the blending of oleophilic polyethylene terephthalate (PET) with low surface energy materials such as fluorinated polyesters has been used in order to fabricate oleophobic PET films. First, fluorinated polyesters (P(PF-oate-R)) possessing different end-groups (-COOH, -OH and -CF3) are synthesized via polycondensation reaction of isophthaloyl chloride with perfluoro ether alcohols. Then, they are solvent-blended with PET at various concentrations to obtain oleophobic polyester films of different compositions. In addition, the films are annealed to investigate the effect of annealing on surface properties of the films. The results show that the obtained PET/P(PF-oate-R) polyester films demonstrate low wettability that depended on the polyester end-groups, film compositions, and annealing. It is found that PET blended with fluorinated polyesters terminated with CF3 groups exhibit higher contact angle (CA) with water and oils than other polyesters. In addition, CA increases with increasing P(PF-oate-R) polyester content in blends. To facilitate the oleophobicity of PET films, the fluorinated polyesters terminated with -CF3 groups with two different Mw were synthesized and blended with PET. The results reveal that at low concentrations, low molecular weight polyesters migrate to the surface easily, resulting in higher surface coverage. Thus, it leads to higher water and oil repellency. On the other hand, when they are used at high concentrations, higher molecular weight polyesters in blends reduce the wettability of the surface to the higher level. It is found that the wettability of the PET film surface depends on not only the Mw of polyesters, but also on annealing protocol. To this end, the effects of the annealing temperature on surface wettability are also examined.

  4. Polyelectrolyte properties of proteoglycan monomers

    Science.gov (United States)

    Li, Xiao; Reed, Wayne F.

    1991-03-01

    Light scattering measurements were made on proteoglycan monomers (PGM) over a wide range of ionic strengths Cs, and proteoglycan concentrations [PG]. At low Cs there were clear peaks in the angular scattering intensity curve I(q), which moved towards higher scattering wave numbers q, as [PG]1/3. This differs from the square root dependence of scattering peaks found by neutron scattering from more concentrated polyelectrolyte solutions. The peaks remained roughly fixed as Cs increased, but diminished in height, and superposed I(q) curves yielded a sort of isosbestic point. Under certain assumptions the static structure factor S(q) could be extracted from the measured I(q), and was found to retain a peak. A simple hypothesis concerning coexisting disordered and liquidlike correlated states is presented, which qualitatively accounts for the most salient features of the peaks. There was evidence of a double component scattering autocorrelation decay at low Cs, which, when resolved into two apparent diffusion coefficients, gave the appearance of simultaneous ``ordinary'' and ``extraordinary'' phases. The extraordinary phase was ``removable,'' however, by filtering. At higher Cs the proteoglycans appear to behave as random nonfree draining polyelectrolyte coils, with a near constant ratio of 0.67 between hydrodynamic radius and radius of gyration. The apparent persistence length varied as roughly the -0.50 power of ionic strength, similar to various linear synthetic and biological polyelectrolytes. Electrostatic excluded volume theory accounted well for the dependence of A2 on Cs.

  5. Controlling monomer-sequence using supramolecular templates

    OpenAIRE

    ten Brummelhuis, Niels

    2014-01-01

    The transcription and translation of information contained in nucleic acids that has been perfected by nature serves as inspiration for chemists to devise strategies for the creation of polymers with welldefined monomer sequences. In this review the various approaches in which templates (either biopolymers or synthetic ones) are used to influence the monomer-sequence are discussed.

  6. Development of Polyester/Eggshell Particulate Composites

    Directory of Open Access Journals (Sweden)

    S.N. Patrick

    2012-12-01

    Full Text Available The development of Polyester/Eggshell particulate composites has been carried out. Uncarbonized and carbonized eggshell particles were used as reinforcement in polyester matrix. 10 to 50 wt% eggshell particles at intervals of 10 wt% were added to polyester as reinforcement. The microstructural analyses of the polyester/eggshell particulate composites were carried out using SEM and EDS. The mechanical properties and density were carried out by standard methods. The results showed that the density and hardness values of the polyester/eggshell particulate composite increased steadily with increasing eggshell addition. The tensile strength increased from 15.182 N/mm2 at 0 wt% eggshell addition to a maximum of 23.4 N/mm2 at 40 wt% eggshell addition for uncarbonized eggshell; while it increased to a maximum of 28.378 N/mm2 at 20 wt% eggshell addition for carbonized eggshell. Compressive strength increased steadily from 90.3 N/mm2 at 0 wt% eggshell additions to a maximum of 103.6 at 50 wt% eggshell addition for uncarbonized eggshell and 116.5N/mm2 at 50 % eggshell addition for carbonized eggshell. Hardness value increased from 91 HRF at 0 % eggshell addition to a maximum of 120.05HRF at 50 wt% eggshell addition for uncarbonized eggshell and 149.45HRF at 50 wt% eggshell for the carbonized eggshell. Flexural strength increased from 76.06 N/mm2 at 0 wt% eggshell addition to a maximum of 97.06 N/mm2 at 40 wt% eggshell addition for uncarbonized eggshell; however, it increased to a maximum of 106.66 N/mm2 at 20 wt% eggshell addition for the carbonized eggshell. The impact energy also increased from 0.1 Joules at 0 wt% eggshell addition to a maximum of 0.35 Joules at 30 wt% eggshell addition for uncarbonized eggshell; it however increased to a maximum of 0.45 Joules at 20 wt% eggshell addition for the carbonized eggshell. Hence the development of polyester/eggshell particulate composites material with good mechanical properties and light weight which is

  7. 75 FR 64694 - Second Antidumping Duty Administrative Review of Certain Polyester Staple Fiber From the People's...

    Science.gov (United States)

    2010-10-20

    ... International Trade Administration Second Antidumping Duty Administrative Review of Certain Polyester Staple... the Preliminary Results of the second administrative review of certain polyester staple fiber (``PSF... Polyester Staple Fiber From the People's Republic of China: Notice of Preliminary Results and...

  8. Thermotropic liquid crystalline polyesters derived from 2-chloro hydroquinone

    Indian Academy of Sciences (India)

    NAGESH MANURKAR; SAYAJI MORE; KHUDBUDIN MULANI; NITIN GANJAVE; NAYAKU CHAVAN

    2017-09-01

    Synthesis of thermotropic liquid crystalline polyesters derived from bis[4-hydroxy benzoyloxy]- 2-chloro-1,4-benzene (BHBOCB) and aliphatic dicarboxylic acid chlorides by interfacial polycondensation methodology is presented. Synthesised polyesters consist of bis[4-hydroxy benzoyloxy]-2-chloro-1,4-benzeneas a mesogen and aliphatic diacid chloride as flexible spacer. The length of oligomethylene units in the polymer was varied from the trimethylene to the dodecamethylene groups. Synthesized polyesters were characterizedby differential scanning calorimetry and optical microscopy. The transition temperatures and thermodynamic properties were studied for all these polymers. These polyesters exhibited thermotropic liquid crystalline behavior and showed nematic texture except decamethylene spacer. Decamethylene spacer based polyester showed marble texture of smectic C. Mesophase stability of these polyesters was higher than 123◦C (except first heating cycle of PE-1).

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

    DEFF Research Database (Denmark)

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

    2006-01-01

    In this article, we describe fabrication of polarisation holographic optical elements in azobenzene polyesters. Both liquid crystalline and amorphous side-chain polyesters have been utilised. Diffractive optical elements such as lenses and gratings that are sensitive to the polarisation...... of the incident light have been fabricated with polarisation holography. Computer-generated optical elements and patterns have also been written with a single polarised laser beam. Recording of polarisation defects enabling easy visualisation is also shown to be feasible in azobenzene polyesters....

  10. Side-chain liquid crystalline polyesters for optical information storage

    DEFF Research Database (Denmark)

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

    1996-01-01

    Azobenzene side-chain liquid crystalline polyester structures suitable for permanent optical storage are described. The synthesis and characterization of the polyesters together with differential scanning calorimetry and X-ray investigations are discussed. Optical anisotropic investigations...... and holographic storage in one particular polyester are described in detail and polarized Fourier transform infrared spectroscopic data complementing the optical data are presented. Optical and atomic force microscope investigations point to a laser-induced aggregation as responsible for permanent optical storage....

  11. Thermal stability of aliphatic hyperbranched polyesters

    Directory of Open Access Journals (Sweden)

    Vuković Jasna

    2002-01-01

    Full Text Available The influence of the molar mass (generation, number and type of end groups on the thermal stability of aliphatic hyperbranched polyesters are presented in this study. Different end groups were obtained by modification of the samples with chlorides of propionic acid and stearic acid. The thermal stability of the hyperbranched polyesters was determined by thermogravimetry using a NET-ZSCH TG 209 instrument in nitrogen atmosphere at a heating rate of 10°C/min. A comparison of the temperatures obtained for mass losses of 5 20 and 40 wt% for unmodified samples showed that the thermal stability increased up to the fourth generation and then remained practically constant. An increase in the thermal stability of modified samples of the second, third and fourth generation was observed.

  12. Studies on Wicking Behaviour of Polyester Fabric

    Directory of Open Access Journals (Sweden)

    Arobindo Chatterjee

    2014-01-01

    Full Text Available This paper aims to investigate vertical wicking properties of polyester fabric based on change in sample direction and change in tension. Also experimental results are compared with theoretical results. Polyester fabric made out of spun yarn with four types of variation in pick density was used. Theoretical values of vertical wicking were calculated by using Lucas-Washburn equation and experimental results were recorded using strip test method. Maximum height reached experimentally in both warp way and weft way is more than that of the theoretical values. The maximum height attained by fabric experimentally in weft is more as compared to warp way. Vertical wicking increases with increase in tension. This paper is focused on wicking which plays a vital role in determining comfort and moisture transport behavior of fabric.

  13. STUDIES ON THE KINETICS OF PHASE TRANSITIONS OF A MAIN CHAIN THERMOTROPIC POLYESTER

    Institute of Scientific and Technical Information of China (English)

    LIU Xiaoping; HU Shiru; SHI Lianghe; XU Mao

    1989-01-01

    The kinetics of phase transitions including a transition between mesophases were studied for a main-chain thermotropic polyester by means of DSC and depolarizing transmittance techniques. The isothermal process of these transitions was found to be described by the Avrami equation to high conversions. The Avrami exponents n are about 2.4, 5.3 and 2.2 for liquid crystallization, transition between mesophases and crystallization from mesophase respectively. The liquid crystallization from isotropic liquid phase occurs at very low undercoolings with high transformation rate. This behavior is explained as the results of the smaller value of the surface free energy for mesophase than that for crystallites which is evidenced by the very weak temperature dependence of liquid crystallization rate.

  14. 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.

  15. Critical behavior in the cubic dimer model at nonzero monomer density

    Science.gov (United States)

    Sreejith, G. J.; Powell, Stephen

    2014-01-01

    We study critical behavior in the classical cubic dimer model (CDM) in the presence of a finite density of monomers. With attractive interactions between parallel dimers, the monomer-free CDM exhibits an unconventional transition from a Coulomb phase to a dimer crystal. Monomers act as charges (or monopoles) in the Coulomb phase and, at nonzero density, lead to a standard Landau-type transition. We use large-scale Monte Carlo simulations to study the system in the neighborhood of the critical point, and find results in agreement with detailed predictions of scaling theory. Going beyond previous studies of the transition in the absence of monomers, we explicitly confirm the distinction between conventional and unconventional criticality, and quantitatively demonstrate the crossover between the two. Our results also provide additional evidence for the theoretical claim that the transition in the CDM belongs in the same universality class as the deconfined quantum critical point in the SU (2) JQ model.

  16. Cyclic Polymer with Alternating Monomer Sequence.

    Science.gov (United States)

    Zhu, Wen; Li, Zi; Zhao, Youliang; Zhang, Ke

    2015-11-01

    Cyclic polymers with alternating monomer sequence are synthesized for the first time based on the ring-closure strategy. Well-defined telechelic alternating polymers are synthesized by reversible addition-fragmentation chain transfer polymerization by copolymerizing the electron acceptor monomer of N-benzylmaleimide and donor monomer of styrene with a feed ratio of 1 between them. The corresponding cyclic alternating polymers are then produced by the UV-induced Diels-Alder click reaction to ring-close the linear alternating polymer precursors under highly diluted reaction solution.

  17. Immobilized Candida antarctica lipase B: Hydration, stripping off and application in ring opening polyester synthesis.

    Science.gov (United States)

    Idris, Ani; Bukhari, Attaullah

    2012-01-01

    This work reviews the stripping off, role of water molecules in activity, and flexibility of immobilized Candida antarctica lipase B (CALB). Employment of CALB in ring opening polyester synthesis emphasizing on a polylactide is discussed in detail. Execution of enzymes in place of inorganic catalysts is the most green alternative for sustainable and environment friendly synthesis of products on an industrial scale. Robust immobilization and consequently performance of enzyme is the essential objective of enzyme application in industry. Water bound to the surface of an enzyme (contact class of water molecules) is inevitable for enzyme performance; it controls enzyme dynamics via flexibility changes and has intensive influence on enzyme activity. The value of pH during immobilization of CALB plays a critical role in fixing the active conformation of an enzyme. Comprehensive selection of support and protocol can develop a robust immobilized enzyme thus enhancing its performance. Organic solvents with a log P value higher than four are more suitable for enzymatic catalysis as these solvents tend to strip away very little of the enzyme surface bound water molecules. Alternatively ionic liquid can work as a more promising reaction media. Covalent immobilization is an exclusively reliable technique to circumvent the leaching of enzymes and to enhance stability. Activated polystyrene nanoparticles can prove to be a practical and economical support for chemical immobilization of CALB. In order to reduce the E-factor for the synthesis of biodegradable polymers; enzymatic ring opening polyester synthesis (eROPS) of cyclic monomers is a more sensible route for polyester synthesis. Synergies obtained from ionic liquids and immobilized enzyme can be much effective eROPS.

  18. Identification of unknown compounds from polyester cans coatings that may potentially migrate into food or food simulants.

    Science.gov (United States)

    Paseiro-Cerrato, Rafael; MacMahon, Shaun; Ridge, Clark D; Noonan, Gregory O; Begley, Timothy H

    2016-04-29

    Cross-linked polyester resins are being introduced into the market as alternatives to epoxy resins as coatings for metal food cans. Identification of potential migrants, from these coatings into food, is a significant analytical challenge due to the diversity of substances employed in the manufacture of the coatings. However, such identification is required to assess migration from the can coating into the food and quantify dietary exposure. Polyester can coatings were extracted with acetonitrile at 40°C for 24h and the extracts were analyzed by a variety of analytical techniques, including GC-MS, HPLC-DAD/MS, HPLC-DAD/CAD and UHPL C-HRMS. Twenty nine non-volatile oligomers were tentatively identified using retention times, UV spectra, and accurate mass measurements. Identified oligomers suggest the coating in use for food cans is a polyester coating and is mainly based on the monomers isophthalic acid, terephthalic acid and nadic acid. To give confidence in the identification, one of the tentatively identified oligomer was synthetized and analyzed by (13)C and (1)H NMR and UHPL C-HRMS. The NMR and HRMS results, confirmed the presence of this compound in the can extracts. Finally, to determine if rapid, direct detection of the oligomers was practical, the coatings were analyzed by DART-HRMS. Twenty three out of the 29 oligomers were identified in the coating by direct measurement with DART-HRMS in few minutes.

  19. New poly(ester urea) derived from L-leucine: electrospun scaffolds loaded with antibacterial drugs and enzymes.

    Science.gov (United States)

    Díaz, Angélica; del Valle, Luis J; Tugushi, David; Katsarava, Ramaz; Puiggalí, Jordi

    2015-01-01

    Electrospun scaffolds from an amino acid containing poly(ester urea) (PEU) were developed as promising materials in the biomedical field and specifically in tissue engineering applications. The selected poly(ester urea) was obtained with a high yield and molecular weight by reaction of phosgene with a bis(α-aminoacyl)-α,ω-diol-diester monomer. The polymer having L-leucine, 1,6-hexanediol and carbonic acid units had a semicrystalline character and relatively high glass transition and melting temperatures. Furthermore it was highly soluble in most organic solvents, an interesting feature that facilitated the electrospinning process and the effective incorporation of drugs with bactericidal activity (e.g. biguanide derivatives such as clorhexidine and polyhexamethylenebiguanide) and enzymes (e.g. α-chymotrypsin) that accelerated the degradation process. Continuous micro/nanofibers were obtained under a wide range of processing conditions, being diameters of electrospun fibers dependent on the drug and solvent used. Poly(ester urea) samples were degradable in media containing lipases and proteinases but the degradation rate was highly dependent on the surface area, being specifically greater for scaffolds with respect to films. The high hydrophobicity of new scaffolds had repercussions on enzymatic degradability since different weight loss rates were found depending on how samples were exposed to the medium (e.g. forced or non-forced immersion). New scaffolds were biocompatible, as demonstrated by adhesion and proliferation assays performed with fibroblast and epithelial cells.

  20. Enzymatic Synthesis and Chemical Recycling of Novel Polyester-Type Thermoplastic Elastomers

    Directory of Open Access Journals (Sweden)

    Tsukuru Yagihara

    2012-06-01

    Full Text Available Novel polyester-type thermoplastic elastomers based on poly(alkylene succinates were synthesized by the lipase-catalyzed copolymerization of cyclic diol/succinate oligomer and cyclic diol/alkylthiosuccinate oligomer. These copolymers exhibited biodegradabilities by activated sludge and a wide range of thermal and mechanical properties that were dependent on the molecular structure and the content of side alkylthio groups. The degree of crystallinity of the copolymer decreased with increasing content of alkylthio groups, which were introduced into the polymer chain as a soft segment. Furthermore, lipase-catalyzed depolymerization of these copolymers into cyclic oligomers and repolymerization of the oligomers was carried out. A repolymerized copolymer having the same Mw and monomer composition as the initial copolymer was obtained, indicating the chemical recyclability of the copolymer.

  1. Preparation and properties of new flame retardant hydrophilic polyester%新型阻燃亲水聚酯纤维的制备及其性能

    Institute of Scientific and Technical Information of China (English)

    方孝芬; 王朝生

    2013-01-01

    由于聚酯纤维回潮率低,染色性差,易积聚静电,易起球,易燃烧,使其应用受限.为了提高聚酯纤维的亲水性和阻燃性能,采用PTA、EG并添加第三单体(SIPE)、第四单体(PEG)和第五单体(亲水剂)进行共聚反应制备高亲水聚酯切片.通过亲水聚酯切片和含共聚阻燃剂(CEPPA,2-羧乙基苯基次膦酸)的阻燃母粒共混熔融纺丝的方法制备具有阻燃功能和高亲水功能的聚酯纤维,并对其阻燃性能和亲水性能进行测试.结果表明,经改性后的聚酯切片热稳定性能与PET相比变化不大,表面接触角小于65°,极限氧指数大于30%,得到的亲水阻燃聚酯的亲水性、热稳定性及阻燃性能良好.%The application of polyester fiber is restricted because of its disadvantages, mainly the low moisture regain, short of chromaticity, easy accumulation of electrostatic charge, easy pilling and easy burning. In order to improve the hydrophilicity of polyester fiber and flame retardant properties, highly hydrophilic polyester chips were prepared by using PTA, EG, the third monomer ( SIPE ) , the fourth monomer ( PEG ) and the fifth monomer ( hydrophilc agent) . Flame-retardant and high hydrophilic polyester fibers were prepared by melt blend spinning of hydrophilic chips and flame retardant masterbatch containing CEPPA. Its flame retardant properties and hydrophilic properties were tested. The analysis results showed that the modified polyester chips exhibited similar thermal stability to that of PET, with contact angle smaller than 65°and limit oxygen index greater than 30% . The hydrophilic polyester has good hydrophilicity, thermal stability and flame retardant properties.

  2. Cross-Linkable Epoxidized Maleinated Castor Oil: A Renewable Resin Alternative to Unsaturated Polyesters

    Directory of Open Access Journals (Sweden)

    Yeşim Müge Şahin

    2016-01-01

    Full Text Available As an alternative resin to conventional synthetic unsaturated polyesters (UPEs, epoxidized maleinated castor oil (EMACO was synthesized in two steps. For this purpose, castor oil was reacted with maleic anhydride at 70°C to obtain maleinated castor oil (MACO. Then, epoxidation of MACO was carried out by using a mixture of formic acid and hydrogen peroxide at 0–5°C. Then, the free carboxyl groups of the synthesized EMACO were further reacted with free epoxide groups of EMACO at 90°C. At the end of the reaction, an unsaturated polyester precursor-prepolymer was obtained (P-EMACO. FTIR and 1H NMR spectroscopic techniques were used to characterize the monomers synthesized. The P-EMACO was then mixed with styrene and cross-linked in the presence of AIBN at 50°C. Thermal and mechanical properties of the final cross-linked product were investigated by thermogravimetric analysis (TGA and dynamic mechanical analysis (DMA techniques. The degradation onset temperature of the material at which cross-linked X-EMACO loses 5% of its weight was found to be 209°C. Its dynamic Tg and storage modulus at 25°C were determined as 72°C and 1.08 GPa, respectively. These results are higher than some of the different oil based polymers reported in the literature.

  3. Local and systemic effects of unpolymerised monomers

    Directory of Open Access Journals (Sweden)

    Sulekha Siddharth Gosavi

    2010-01-01

    Full Text Available Methyl methacrylate (MMA, a widely used monomer in dentistry and medicine has been reported to cause abnormalities or lesions in several organs. Experimental and clinical studies have documented that monomers may cause a wide range of adverse health effects such as irritation to skin, eyes, and mucous membranes, allergic dermatitis, stomatitis, asthma, neuropathy, disturbances of the central nervous system, liver toxicity, and fertility disturbances.

  4. A biocatalytic approach towards sustainable furanic-aliphatic polyesters

    NARCIS (Netherlands)

    Jiang, Yi; Woortman, Albert J. J.; van Ekenstein, Gert O. R. Alberda; Loos, Katja

    2015-01-01

    An eco-friendly approach towards furanic-aliphatic polyesters as sustainable alternatives to aromatic-aliphatic polyesters is presented. In this approach, biobased dimethyl 2,5-furandicarboxylate (DMFDCA) is polymerized with various (potentially) renewable aliphatic diols via Candida antarctica

  5. 40 CFR 721.6485 - Hydroxy terminated polyester.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Hydroxy terminated polyester. 721.6485... Substances § 721.6485 Hydroxy terminated polyester. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a hydroxy terminated...

  6. 75 FR 23300 - Greige Polyester/Cotton Printcloth From China

    Science.gov (United States)

    2010-05-03

    ... COMMISSION Greige Polyester/Cotton Printcloth From China AGENCY: United States International Trade Commission.../cotton printcloth from China. SUMMARY: The Commission hereby gives notice that it has instituted a review... revocation of the antidumping duty order on greige polyester/cotton printcloth from China would be likely...

  7. 75 FR 42784 - Greige Polyester/Cotton Printcloth From China

    Science.gov (United States)

    2010-07-22

    ... COMMISSION Greige Polyester/Cotton Printcloth From China AGENCY: United States International Trade Commission... to determine whether revocation of the antidumping duty order on greige polyester/cotton printcloth from China would be likely to lead to continuation or recurrence of material injury. On July 2,...

  8. Surface modification of polyester biomaterials for tissue engineering.

    Science.gov (United States)

    Jiao, Yan-Peng; Cui, Fu-Zhai

    2007-12-01

    Surfaces play an important role in a biological system for most biological reactions occurring at surfaces and interfaces. The development of biomaterials for tissue engineering is to create perfect surfaces which can provoke specific cellular responses and direct new tissue regeneration. The improvement in biocompatibility of biomaterials for tissue engineering by directed surface modification is an important contribution to biomaterials development. Among many biomaterials used for tissue engineering, polyesters have been well documented for their excellent biodegradability, biocompatibility and nontoxicity. However, poor hydrophilicity and the lack of natural recognition sites on the surface of polyesters have greatly limited their further application in the tissue engineering field. Therefore, how to introduce functional groups or molecules to polyester surfaces, which ideally adjust cell/tissue biological functions, becomes more and more important. In this review, recent advances in polyester surface modification and their applications are reviewed. The development of new technologies or methods used to modify polyester surfaces for developing their biocompatibility is introduced. The results of polyester surface modifications by surface morphological modification, surface chemical group/charge modification, surface biomacromolecule modification and so on are reported in detail. Modified surface properties of polyesters directly related to in vitro/vivo biological performances are presented as well, such as protein adsorption, cell attachment and growth and tissue response. Lastly, the prospect of polyester surface modification is discussed, especially the current conception of biomimetic and molecular recognition.

  9. Mechanism of Reduction Action of Unsaturated Polyester Resin

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The reduction action mechanism of the unsatrurated polyester resin reducer is analysed by the free space volume theory.Through measuring the reduction magnitude in each phase of solidification,the authors predicted the rate of reduction is in concordance with the results from experiments.From this we presented corresponding solutions to different causes of the reduction action of the unsaturated polyester resin.

  10. Vanadium Trineodecanoate Promoter for Fiberglass-Polyester Soil Surfacings.

    Science.gov (United States)

    1980-06-01

    surfaces for soils consists of a polyester resin, cumene hydroperoxide catalyst and a promoter solution containing a vanadium salt and N,N-dimethyl-p-tolui...4 Synthesis of Vanadium Trineodecanoate .. .... ......... 4 Reactions Using Various Reagents. ..... ........... 4 Analysis of Vanadium...polymer system consists of a polyester resin, a peroxide cata- lyst ( cumene hydroperoxide) and a two-part, premixed, promoter solution. The promoter

  11. Microbial degradation of polyurethane, polyester polyurethanes and polyether polyurethanes.

    Science.gov (United States)

    Nakajima-Kambe, T; Shigeno-Akutsu, Y; Nomura, N; Onuma, F; Nakahara, T

    1999-02-01

    Polyurethane (PUR) is a polymer derived from the condensation of polyisocyanate and polyol and it is widely used as a base material in various industries. PUR, in particular, polyester PUR, is known to be vulnerable to microbial attack. Recently, environmental pollution by plastic wastes has become a serious issue and polyester PUR had attracted attention because of its biodegradability. There are many reports on the degradation of polyester PUR by microorganisms, especially by fungi. Microbial degradation of polyester PUR is thought to be mainly due to the hydrolysis of ester bonds by esterases. Recently, polyester-PUR-degrading enzymes have been purified and their characteristics reported. Among them, a solid-polyester-PUR-degrading enzyme (PUR esterase) derived from Comamonas acidovorans TB-35 had unique characteristics. This enzyme has a hydrophobic PUR-surface-binding domain and a catalytic domain, and the surface-binding domain was considered as being essential for PUR degradation. This hydrophobic surface-binding domain is also observed in other solid-polyester-degrading enzymes such as poly(hydroxyalkanoate) (PHA) depolymerases. There was no significant homology between the amino acid sequence of PUR esterase and that of PHA depolymerases, except in the hydrophobic surface-binding region. Thus, PUR esterase and PHA depolymerase are probably different in terms of their evolutionary origin and it is possible that PUR esterases come to be classified as a new solid-polyester-degrading enzyme family.

  12. 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

    2016-01-05

    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.

  13. Synthesis of the diazonium (perfluoroalkyl) benzenesulfonimide monomer from Nafion monomer for proton exchange membrane fuel cells

    Science.gov (United States)

    Mei, Hua; D'Andrea, Dan; Nguyen, Tuyet-Trinh; Nworie, Chima

    2014-02-01

    One diazonium (perfluoroalkyl) benzenesulfonimide monomer, perfluoro-3, 6-dioxa-4-methyl-7-octene benzenesulfonyl imide, has been synthesized from Nafion monomer for the first time. With trifluorovinyl ether and diazonium precursors, the partially-fluorinated diazonium PFSI monomer can be polymerized and will provide chemically bonding with carbon electrode in proton exchange membrane fuel cells. A systematic study of the synthesis and characterization of this diazonium PFSI monomer has been conducted by varying reaction conditions. The optimized synthesis method has been established in the lab.

  14. Polyester mooring stiffness modeling for deepwater floating system

    Institute of Scientific and Technical Information of China (English)

    Chen Yongjun; Qu Yan; Zhang Tianyu

    2013-01-01

    Polyester mooring has become increasing popular to serve as permanent station-keeping system for deepwater floating system during recent years.Comparing to the traditional steel wire mooring,polyester mooring provides significant benefits in deepwater,such as reduced installed capital expenditure (CAPEX) and smaller vertical loads on host platform.Polyester rope is a visco-elastic material,and its stiffness is nonlinear and affected by mean load,load range,loading period and loading history.There is a perception that the polyester stiffness model has significant impact on the floating system' s performance.This paper presents a detailed description and comparison of two stiffness models and three analytic approaches,and provides a systematic study of the impact of polyester mooring stiffness modeling on the deepwater floating system performance.

  15. 聚酯水性化技术及水性聚酯稳定性研究进展%Development in waterborn technology and product stability of waterborne polyester resins

    Institute of Scientific and Technical Information of China (English)

    刘身凯; 胡剑青; 涂伟萍

    2009-01-01

    The water-borne technology for polyester is reviewed with using different hydrophilic monomers, including trimellitic anhydride, dimethylmalonic acid, UV curable hyperbranched waterborne polyester, as well as sulphonate monomer. Methods to enhance the water resistant performance of the waterborne polyester and the related theory are summarized. The possible trends in development of waterborne polyester resins are prospected.%综述了4种含有不同亲水单体的聚酯水性化技术,包括传统型的以偏苯三酸酐为亲水性单体的水性聚酯、二羟甲基丙酸为亲水性单体的水性聚酯、紫外固化超支化水性聚酯以及磺酸盐型单体的水性聚酯.在此基础上,叙述了提高水性聚酯耐水解稳定性的方法及原理,并指出了水性聚酯的发展趋势.

  16. High-Throughput Analysis of Enzymatic Hydrolysis of Biodegradable Polyesters by Monitoring Cohydrolysis of a Polyester-Embedded Fluorogenic Probe.

    Science.gov (United States)

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

    2017-02-14

    Biodegradable polyesters have the potential to replace nondegradable, persistent polymers in numerous applications and thereby alleviate plastic accumulation in the environment. Herein, we present an analytical approach to study enzymatic hydrolysis of polyesters, the key step in their overall biodegradation process. The approach is based on embedding fluorescein dilaurate (FDL), a fluorogenic ester substrate, into the polyester matrix and on monitoring the enzymatic cohydrolysis of FDL to fluorescein during enzymatic hydrolysis of the polyester. We validated the approach against established techniques using FDL-containing poly(butylene adipate) films and Fusarium solani cutinase (FsC). Implemented on a microplate reader platform, the FDL-based approach enabled sensitive and high-throughput analysis of the enzymatic hydrolysis of eight aliphatic polyesters by two fungal esterases (FsC and Rhizopus oryzae lipase) at different temperatures. While hydrolysis rates for both enzymes increased with decreasing differences between the polyester melting temperatures and the experimental temperatures, this trend was more pronounced for the lipase than the cutinase. These trends in rates could be ascribed to a combination of temperature-dependent polyester chain flexibility and accessibility of the enzyme active site. The work highlights the capability of the FDL-based approach to be utilized in both screening and mechanistic studies of enzymatic polyester hydrolysis.

  17. Polyester textile functionalization through incorporation of pH/thermo-responsive microgels. Part II: polyester functionalization and characterization

    NARCIS (Netherlands)

    Glampedaki, P.; Calvimontes, A.; Dutschk, V.; Warmoeskerken, M.M.C.G.

    2012-01-01

    A new approach to functionalize the surface of polyester textiles is described in this study. Functionalization was achieved by incorporating pH/temperature-responsive polyelectrolyte microgels into the textile surface layer using UV irradiation. The aim of functionalization was to regulate polyeste

  18. 78 FR 51707 - Certain Polyester Staple Fiber From the Republic of Korea: Rescission of Antidumping Duty...

    Science.gov (United States)

    2013-08-21

    ... International Trade Administration Certain Polyester Staple Fiber From the Republic of Korea: Rescission of... administrative review of the antidumping duty order on certain polyester staple fiber (polyester staple fiber... antidumping duty order on polyester staple fiber from Korea for the period May 1, 2012, through April 30,...

  19. 76 FR 57955 - Certain Polyester Staple Fiber From Taiwan: Final Results of Antidumping Duty Administrative Review

    Science.gov (United States)

    2011-09-19

    ... International Trade Administration Certain Polyester Staple Fiber From Taiwan: Final Results of Antidumping Duty... administrative review of the antidumping duty order on certain polyester staple fiber from Taiwan. The period of... certain polyester staple fiber from Taiwan. See Certain Polyester Staple Fiber From Taiwan:...

  20. Reactive modification of polyesters and their blends

    Science.gov (United States)

    Wan, Chen

    2004-12-01

    As part of a broader research effort to investigate the chemical modification of polyesters by reactive processing a low molecular weight (MW) unsaturated polyester (UP) and a higher MW saturated polyester, polyethylene terephthalate (PET), alone or blended with polypropylene (PP) were melt processed in a batch mixer and continuous twin screw extruders. Modification was monitored by on-line rheology and the products were characterized primarily by off-line rheology, morphology and thermal analysis. Efforts were made to establish processing/property relationships and provide an insight of the accompanying structural changes. The overall response of the reactively modified systems was found to be strongly dependent on the component characteristics, blend composition, type and concentrations of reactive additives and processing conditions. The work concluded that UP can be effectively modified through reactive melt processing. Its melt viscosity and MW can be increased through chemical reactions between organic peroxides (POX) and chain unsaturation or between MgO and carboxyl/hydroxyl end groups. Reactive blending of PP/UP blends through peroxide modification gave finer and more uniform morphology than unreacted blends and at a given PP/UP weight ratio more thermoplastic elastomers-like rheological behavior. This is due to the continuously decreasing viscosity ratio of PP/UP towards unity by the competing reactions between POX and the blend components and formation of PP-UP copolymers which serve as in-situ compatibilizers to promote better interfacial adhesion. Kinetics of the competing reactions were analyzed through a developed model. In addition to POX concentration and mixing efficiency, rheology and morphology of UP/PP bends were significantly affected by the addition of inorganic and organic coagents. Addition of coagents such as a difunctional maleimide, MgO and/or an anhydride functionalized PP during reactive blending offers effective means for tailoring

  1. Preparation of Polyester-Based Metal-Cross Linked Polymeric Composites as Novel Materials Resistant to Bacterial Adhesion and Biofilm Formation

    Directory of Open Access Journals (Sweden)

    Mutasem O. Taha

    2011-01-01

    Full Text Available Bacterial biofilms constitute an extremely resistant form of bacterial colonization with dire health and economical implications. Towards achieving polymeric composites capable of resisting bacterial adhesion and biofilm formation, we prepared five 2,6-pyridinedicarboxylate-based polyesters employing five different diol monomers. The resulting polyesters were complexed with copper (II or silver (I. The new polymers were characterized by proton and carbon nuclear magnetic resonance spectroscopy, inherent viscosity, infrared spectroscopy, differential scanning calorimetry and thermogravimetric analysis. The corresponding metal complexes were characterized by differential scanning calorimery and infrared spectroscopy. The amounts of complexed copper and silver were determined by atomic absorption spectrophotometry. Finally, the resulting composites were tested for their antibacterial potential and were found to effectively resist bacterial attachment and growth.

  2. Polymerization of 10,16-dihydroxyhexadecanoic acid, main monomer of tomato cuticle, using the Lewis acidic ionic liquid choline chloride.2ZnCl2

    Directory of Open Access Journals (Sweden)

    Mayra Beatriz eGómez-Patiño

    2015-11-01

    Full Text Available 10,16-dihydroxyhexadecanoic acid, main monomer of the tomato cuticle obtained from agro-residual wastes, was polymerized using (choline chloride.2ZnCl2 ionic liquid as catalyst at three different temperatures (80, 90 and 100 °C. The resulting polyesters obtained under these conditions were insoluble in most of the organic solvents and showed different physicochemical properties. While at 80 °C polymers were obtained as powder, at higher temperature they were found in viscous consistency. According with the CP MAS 13C NMR and FTIR-ATR analysis, polymers showed a linear structure with an increasing degree of esterification in position C-10. Polyesters were analyzed by means of differential scanning calorimetry (DSC, atomic force microscopy (AFM and X ray diffraction (small- and wide-angle scattering, SWAXS techniques.

  3. Probing the molecular design of hyper-branched aryl polyesters towards lubricant applications

    Science.gov (United States)

    Robinson, Joshua W.; Zhou, Yan; Bhattacharya, Priyanka; Erck, Robert; Qu, Jun; Bays, J. Timothy; Cosimbescu, Lelia

    2016-01-01

    We report novel polymeric materials that may be used as viscosity index improvers (VII) for lubricant applications. Our efforts included probing the comb-burst hyper-branched aryl polyester architecture for beneficial viscosity and friction behavior when utilized as an additive in a group I oil. The monomer was designed as to undergo polymerization via polycondensation within the architectural construct (AB2), typical of hyperbranched polymers. The monomer design was comprised of aliphatic arms (12 or 16 methylenes) to provide the necessary lipophilicity to achieve solubility in a non-polar medium. Once polymerized, via catalyst and heat, the surface alcohols were functionalized with fatty acids (lauric and palmitic). Controlling the aliphatic nature of the internal arms and peripheral end-groups provided four unique flexible polymer designs. Changing the reaction time and concentration provided opportunities to investigate the influence of molecular weight and branching density on oil-solubility, viscosity, and friction. Oil-solubility was found to decrease with fewer internal carbons, but the number of internal carbons appears to have little influence on the bulk solution viscosity. At concentrations of 2 wt % in a group I base oil, these polymer additives demonstrated an improved viscosity index and reduced friction coefficient, validating the basic approach.

  4. Probing the molecular design of hyper-branched aryl polyesters towards lubricant applications.

    Science.gov (United States)

    Robinson, Joshua W; Zhou, Yan; Bhattacharya, Priyanka; Erck, Robert; Qu, Jun; Bays, J Timothy; Cosimbescu, Lelia

    2016-01-01

    We report novel polymeric materials that may be used as viscosity index improvers (VII) for lubricant applications. Our efforts included probing the comb-burst hyper-branched aryl polyester architecture for beneficial viscosity and friction behavior when utilized as an additive in a group I oil. The monomer was designed as to undergo polymerization via polycondensation within the architectural construct (AB2), typical of hyperbranched polymers. The monomer design was comprised of aliphatic arms (12 or 16 methylenes) to provide the necessary lipophilicity to achieve solubility in a non-polar medium. Once polymerized, via catalyst and heat, the surface alcohols were functionalized with fatty acids (lauric and palmitic). Controlling the aliphatic nature of the internal arms and peripheral end-groups provided four unique flexible polymer designs. Changing the reaction time and concentration provided opportunities to investigate the influence of molecular weight and branching density on oil-solubility, viscosity, and friction. Oil-solubility was found to decrease with fewer internal carbons, but the number of internal carbons appears to have little influence on the bulk solution viscosity. At concentrations of 2 wt % in a group I base oil, these polymer additives demonstrated an improved viscosity index and reduced friction coefficient, validating the basic approach.

  5. Cationically polymerizable monomers derived from renewable sources

    Energy Technology Data Exchange (ETDEWEB)

    Crivello, J.V.

    1992-10-01

    The objectives of this project are to design and synthesize novel monomers which orginate from renewable biological sources and to carry out their rapid, efficient, pollution-free and energy efficient cationic polymerization to useful products under the influence of ultraviolet light or heat. A summary of the results of the past year's research on cationically polymerizable monomers derived from renewable sources is presented. Three major areas of investigation corresponding to the different classes of naturally occurring starting materials were investigated; epoxidized terpenes and natural rubber and vinyl ethers from alcohols and carbohydrates.

  6. Cationically polymerizable monomers derived from renewable sources

    Energy Technology Data Exchange (ETDEWEB)

    Crivello, J.V.

    1992-10-01

    The objectives of this project are to design and synthesize novel monomers which orginate from renewable biological sources and to carry out their rapid, efficient, pollution-free and energy efficient cationic polymerization to useful products under the influence of ultraviolet light or heat. A summary of the results of the past year's research on cationically polymerizable monomers derived from renewable sources is presented. Three major areas of investigation corresponding to the different classes of naturally occurring starting materials were investigated; epoxidized terpenes and natural rubber and vinyl ethers from alcohols and carbohydrates.

  7. Lipase-catalyzed synthesis of aliphatic polyesters via copolymerization of lactone, dialkyl diester, and diol.

    Science.gov (United States)

    Jiang, Zhaozhong

    2008-11-01

    Candida antarctica lipase (CALB) has been successfully used as catalyst for copolymerization of dialkyl diester with diol and lactone to form aliphatic polyesters. The polymerization reactions were performed using a two stage process: first stage oligomerization under low vacuum followed by second stage polymerization under high vacuum. Use of the two-stage process is required to obtain products with high molecular weights at high yields for the following reasons: (i) the first stage reaction ensures that the monomer loss via evaporation is minimized to maintain 1:1 diester to diol stoichiometric ratio, and the monomers are converted to nonvolatile oligomers; (ii) use of high vacuum during the second stage accelerates equilibrium transesterification reactions to transform the oligomers to high molecular weight polymers. Thus, terpolymers of omega-pentadecalactone (PDL), diethyl succinate (DES), and 1,4-butanediol (BD) with a M w of whole product (nonfractionated) up to 77000 and M w/ M n between 1.7 and 4.0 were synthesized in high yields (e.g., 95% isolated yield). A desirable reaction temperature for the copolymerizations was found to be around 95 degrees C. At 1:1:1 PDL/DES/BD monomer molar ratio, the resultant terpolymers contained equal moles of PDL, succinate, and butylene repeat units in the polymer chains. (1)H and (13)C NMR analyses were used to determine the polyester microstructures. The synthesized PDL-DES-BD terpolymers possessed near random structures with all possible combinations of PDL, succinate, and butylene units via ester linkages in the polymer backbone. Furthermore, thermal stability and crystallinity of a pure PDL-DES-BD terpolymer with 1:1:1 PDL to succinate to butylene unit ratio and M w of 85400 were studied by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The copolyester was found to be a semicrystalline material with a T g of -34 degrees C and a T m of 64 degrees C, which degrades in a single weight loss

  8. Phase separation during radiation crosslinking of unsaturated polyester resin

    Science.gov (United States)

    Pucić, Irina; Ranogajec, Franjo

    2003-06-01

    Phase separation during radiation-initiated crosslinking of unsaturated polyester resin was studied. Residual reactivity of liquid phases and gels of partially cured samples was determined by DSC. Uncured resin and liquid phases showed double reaction exotherm, gels had a single maximum that corresponded to higher-temperature maximum of liquid parts. The lower-temperature process was attributed to styrene-polyester copolymerization. At higher temperatures, polyester unsaturations that remained unreacted due to microgel formation homopolymerized. FTIR revealed different composition of phases. In thicker samples, reaction heat influenced microgel formation causing delayed appearance of gel and faster increase in conversion.

  9. Softening and elution of monomers in ethanol

    DEFF Research Database (Denmark)

    Benetti, Ana Raquel; Asmussen, Erik; Munksgaard, E Christian;

    2009-01-01

    The purpose of this study was to investigate the effect of light-curing protocol on softening and elution of monomers in ethanol as measured on a model polymer. It was a further aim to correlate the measured values with previously reported data on degree of conversion and glass transition tempera...

  10. Producing monomers and polymers from plant oils

    Science.gov (United States)

    The integration of biobased industrial products into existing markets, where petrochemically-derived materials currently dominate, is a worthy objective. This chapter reviews some technologies that have been developed including olefins of various chain lengths, photo-curable polymers, vinyl monomers...

  11. Nanoridges that characterize the surface morphology of flowers require the synthesis of cutin polyester.

    Science.gov (United States)

    Li-Beisson, Yonghua; Pollard, Mike; Sauveplane, Vincent; Pinot, Franck; Ohlrogge, John; Beisson, Fred

    2009-12-22

    Distinctive nanoridges on the surface of flowers have puzzled plant biologists ever since their discovery over 75 years ago. Although postulated to help attract insect pollinators, the function, chemical nature, and ontogeny of these surface nanostructures remain uncertain. Studies have been hampered by the fact that no ridgeless mutants have been identified. Here, we describe two mutants lacking nanoridges and define the biosynthetic pathway for 10,16-dihydroxypalmitate, a major cutin monomer in nature. Using gene expression profiling, two candidates for the formation of floral cutin were identified in the model plant Arabidopsis thaliana: the glycerol-3-phosphate acyltransferase 6 (GPAT6) and a member of a cytochrome P450 family with unknown biological function (CYP77A6). Plants carrying null mutations in either gene produced petals with no nanoridges and no cuticle could be observed by either scanning or transmission electron microscopy. A strong reduction in cutin content was found in flowers of both mutants. In planta overexpression suggested GPAT6 preferentially uses palmitate derivatives in cutin synthesis. Comparison of cutin monomer profiles in knockouts for CYP77A6 and the fatty acid omega-hydroxylase CYP86A4 provided genetic evidence that CYP77A6 is an in-chain hydroxylase acting subsequently to CYP86A4 in the synthesis of 10,16-dihydroxypalmitate. Biochemical activity of CYP77A6 was demonstrated by production of dihydroxypalmitates from 16-hydroxypalmitate, using CYP77A6-expressing yeast microsomes. These results define the biosynthetic pathway for an abundant and widespread monomer of the cutin polyester, show that the morphology of floral surfaces depends on the synthesis of cutin, and identify target genes to investigate the function of nanoridges in flower biology.

  12. Release of monomers from composite dust.

    Science.gov (United States)

    Cokic, S M; Duca, R C; Godderis, L; Hoet, P H; Seo, J W; Van Meerbeek, B; Van Landuyt, K L

    2017-05-01

    Dental personnel are more at risk to develop asthmatic disease, but the exact reason is so far unknown. During abrasive procedures, dental personnel are exposed to nano-sized dust particles released from dental composite. The aim of this study was to investigate whether respirable composite dust may also release monomers. Respirable (composite dust was collected and the release of methacrylate monomers and Bisphenol A (BPA) in water and ethanol was evaluated by liquid chromatography/mass spectroscopy (LC-MS/MS). The dust was ultra-morphologically and chemically analyzed by transmission electron microscopy and energy-dispersive X-ray spectroscopy (TEM-EDS). LC-MS/MS analysis revealed that, irrespective of the type of composite, the respirable fraction of composite dust may release relatively high concentrations of unpolymerized methacrylate monomers, both in water and ethanol. Higher release was observed in ethanol. The endocrine disruptor BPA also emanated from the composite dust particles. TEM showed that most particles were nano-sized, although particle size ranged between 6nm and 5μm with a mode value between 12 and 39nm. Most particles consisted of several filler particles in resin matrix, although single nano-filler particles could also be observed. Elemental analysis by TEM-EDS proved that the particles collected on the filters originated from the dental composites. Theoretically, composite dust may function as a vehicle to transport monomers deeply into the respiratory system. The results of this study may shed another light on the increasing incidence of respiratory disease among dental personnel, and more care should be taken to prevent inhalation of composite dust. Special care should be taken to prevent inhalation of composite dust, as the dust particles may release methacrylate monomers. Copyright © 2017 Elsevier Ltd. All rights reserved.

  13. Anchoring Strength of Thin Aligned-Polymer Films Formed by Liquid Crystalline Monomer

    Science.gov (United States)

    Murashige, Takeshi; Fujikake, Hideo; Ikehata, Seiichiro; Sato, Fumio

    2003-04-01

    We have evaluated the polar anchoring strength of a thin molecule-aligned polymer film formed by a liquid crystalline monomer. The polymer film was obtained by photopolymerization of the monomer oriented by a rubbed polyimide alignment layer in a chamber filled with N2 gas. We fabricated a nematic liquid crystal cell using the thin aligned-polymer films as alignment layers, and then evaluated the anchoring strength of the polymer by measuring the optical retardation curve of the cell driven by voltages. The experimental result showed that the anchoring strength was one order of magnitude lower than that of a conventional rubbed polyimide alignment layer, and decreased with increasing the cure temperature of the monomer film.

  14. Synthetic polyester-hydrolyzing enzymes from thermophilic actinomycetes.

    Science.gov (United States)

    Wei, Ren; Oeser, Thorsten; Zimmermann, Wolfgang

    2014-01-01

    Thermophilic actinomycetes produce enzymes capable of hydrolyzing synthetic polyesters such as polyethylene terephthalate (PET). In addition to carboxylesterases, which have hydrolytic activity predominantly against PET oligomers, esterases related to cutinases also hydrolyze synthetic polymers. The production of these enzymes by actinomycetes as well as their recombinant expression in heterologous hosts is described and their catalytic activity against polyester substrates is compared. Assays to analyze the enzymatic hydrolysis of synthetic polyesters are evaluated, and a kinetic model describing the enzymatic heterogeneous hydrolysis process is discussed. Structure-function and structure-stability relationships of actinomycete polyester hydrolases are compared based on molecular dynamics simulations and recently solved protein structures. In addition, recent progress in enhancing their activity and thermal stability by random or site-directed mutagenesis is presented.

  15. Highly Branched Bio-Based Unsaturated Polyesters by Enzymatic Polymerization

    DEFF Research Database (Denmark)

    Nguyen, Hiep Dinh; Löf, David; Hvilsted, Søren

    2016-01-01

    A one-pot, enzyme-catalyzed bulk polymerization method for direct production of highly branched polyesters has been developed as an alternative to currently used industrial procedures. Bio-based feed components in the form of glycerol, pentaerythritol, azelaic acid, and tall oil fatty acid (TOFA....... This allows simple variations in the molar mass and structure of the polyester without premature gelation, thus enabling easy tailoring of the branched polyester structure. The postpolymerization crosslinking of the polyesters illustrates their potential as binders in alkyds. The formed films had good UV...... stability, very high water contact angles of up to 141° and a glass transition temperature that could be controlled through the feed composition....

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

    DEFF Research Database (Denmark)

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

    2002-01-01

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

  17. STUDY ON THE SYNTHESIS AND PHYSICOCHEMICAL PROPERTIES OF SUCROSE POLYESTER

    Institute of Scientific and Technical Information of China (English)

    LIU Zhongdong; LIU Huihua; LUO Peng; LIU Peng; Xiao Fugang

    2006-01-01

    Orthogonal test was used to evaluate the effects of synthetic such as temperature (120~140 ℃), reaction time (4-6) and substrate molar ratio of methyl oleate to sucrose (8:1-12:1) on the percent quantity conversion to sucrose polyester. Sucrose polyester was synthesized by a solvent-free one-stage interesterification. The optimum reaction conditions are as follows: methyl oleate/sucrose = 10∶1 (mol/mol); reaction temperature is 140 ℃;yield reaches 88.15%, and the degree of esterification (DE) is over 7 in the conditions. Thin layer chromatography (TLC), column chromatography (CC), High-performance liquid chromatography (HPLC) were used to analyze the product, the results show that the percent of sucrose polyoleate is over 70% in the product. The physicochemical properties of sucrose polyesters were compared with cooking oil. The results show that the qualities of sucrose polyesters are all up to the triglyceride.

  18. Bright Prospect for the Polyester Industrial Filament Sector

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    @@ Some large companies from Americaand Europe have constructed plantsin China or established long-termstable cooperation relationship withChinese enterprises. A bright devel-opment prospect has therefore beenbrought to the polyester industrial fila-ment sector in China.

  19. Nano-biocomposites based on synthetic aliphatic polyesters and nanoclay

    CSIR Research Space (South Africa)

    Ojijo, Vincent O

    2014-05-01

    Full Text Available This article gives an overview of the recent developments in the preparation, characterisation, properties, crystallisation behaviour, and melt rheology of clay-containing composites of biodegradable synthetic aliphatic polyesters such as poly...

  20. Amino alcohol-based degradable poly(ester amide) elastomers

    NARCIS (Netherlands)

    C.J. Bettinger (Christopher); J.P. Bruggeman (Joost); J.T. Borenstein (Jeffrey); R.S. Langer (Robert)

    2008-01-01

    textabstractCurrently available synthetic biodegradable elastomers are primarily composed of crosslinked aliphatic polyesters, which suffer from deficiencies including (1) high crosslink densities, which results in exceedingly high stiffness, (2) rapid degradation upon implantation, or (3) limited c

  1. STUDY ON POLYSULFONE-POLYESTER BLOCK COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    DING Youjun; QI Daquan

    1988-01-01

    Synthesis and characterization of a series of Polysulfone (PSF)-Polyester (PEs) block copolymers were studied.The degree of randomness (B) of these block copolymers was calculated from the intensities of their proton signals in 1H NMR spectra and lies in the region of 0 < B < 1. It was shown that the degree of randomness (B) and the average sequence length (L) in block copolymers were relatively dependent on the reaction conditions, various feed ratios and structure of diols.The phenomenon was observed, when the PSF-PEs block copolymers dissolved in different solvents they had different viscosities and molecular conformations.The PSF-PEs block copolymers had better solvent resistance than homo-polysulfone.

  2. Intra- And Inter-Monomer Interactions are Required to Synergistically Facilitate ATP Hydrolysis in HSP90

    Energy Technology Data Exchange (ETDEWEB)

    Cunningham, C.N.; Krukenberg, K.A.; Agard, D.A.

    2009-05-12

    Nucleotide-dependent conformational changes of the constitutively dimeric molecular chaperone Hsp90 are integral to its molecular mechanism. Recent full-length crystal structures (Protein Data Bank codes 2IOQ, 2CG9, AND 2IOP) of Hsp90 homologs reveal large scale quaternary domain rearrangements upon the addition of nucleotides. Although previous work has shown the importance of C-terminal domain dimerization for efficient ATP hydrolysis, which should imply cooperativity, other studies suggest that the two ATPases function independently. Using the crystal structures as a guide, we examined the role of intra- and intermonomer interactions in stabilizing the ATPase activity of a single active site within an intact dimer. This was accomplished by creating heterodimers that allow us to differentially mutate each monomer, probing the context in which particular residues are important for ATP hydrolysis. Although the ATPase activity of each monomer can function independently, we found that the activity of one monomer could be inhibited by the mutation of hydrophobic residues on the trans N-terminal domain (opposite monomer). Furthermore, these trans interactions are synergistically mediated by a loop on the cis middle domain. This loop contains hydrophobic residues as well as a critical arginine that provides a direct linkage to the {gamma}-phosphate of bound ATP. Small angle x-ray scattering demonstrates that deleterious mutations block domain closure in the presence of AMPPNP (5{prime}-adenylyl-{beta},{gamma}-imidodiphosphate), providing a direct linkage between structural changes and functional consequences. Together, these data indicate that both the cis monomer and the trans monomer and the intradomain and interdomain interactions cooperatively stabilize the active conformation of each active site and help explain the importance of dimer formation.

  3. Characterization of material composite marble-polyester

    Directory of Open Access Journals (Sweden)

    Corpas, F. A.

    2002-12-01

    Full Text Available In this work we characterize a new material composite, formed with a polyester and crushed white marble mixture. The final purpose is double: to obtain a material for applications sufficiently competitive after an economic viability study, increasing the yield of the main commodity, using waste marble and improving the jobs in the quarries area. From the results obtained, we deduce then that this material could be used to inside and outside adornment.

    En este trabajo, caracterizamos un nuevo material compuesto, formado con una mezcla de poliéster y de mármol blanco triturado. El propósito final es doble: por un lado obtener un material para aplicaciones lo suficientemente competitivas como para que se pueda iniciar un estudio económico de viabilidad, aumentando el rendimiento de la materia prima y mejorando las salidas laborales de las comarcas extractoras. Para la caracterización del material se ha determinado el porcentaje adecuado de poliéster. Así como las propiedades mecánicas (flexión, compresión y dureza, químicas, fatiga térmica y su influencia a la exposición solar In order to characterized of material, we have determined the suitable porcentage of polyester Also we have carried out a study of the mechanical (stretching, resistance to traction, hardeness and thermal fatigue chemicals properties and solar radiation influence. De los resultados obtenidos, este material podría ser utilizado para ornamentación tanto de interior como de exterior.

  4. WATER-BASED CROSSLINKABLE COATINGS VIA MINIEMULSION POLYMERIZATION OF ACRYLIC MONOMERS IN THE PRESENCE OF UNSATURATED POLYESTER RESIN. (R825326)

    Science.gov (United States)

    The perspectives, information and conclusions conveyed in research project abstracts, progress reports, final reports, journal abstracts and journal publications convey the viewpoints of the principal investigator and may not represent the views and policies of ORD and EPA. Concl...

  5. THE GAS TRANSPORT BEHAVIOR IN AROMATIC POLYESTER MEMBRANES

    Institute of Scientific and Technical Information of China (English)

    ZHANG Jian; SUN Qiushi; HOU Xiaohuai

    1996-01-01

    Six aromatic polyesters were prepared for gas separation membranes, and their permeation properties for hydrogen, oxygen, nitrogen, carbon dioxide, and methane were measured at 30℃ and 1 atmosphere by low pressure manometric method. The correlation between the gas transport behavior and molecular structure of aromatic polyester membrane is discussed. These data are interpreted qualitatively in terms of the calculated packing density, gas-polymer interaction, concentration of aryl bromine on backbone, and effect of silane group on main chain of polymer.

  6. Synthesis and characterization of gelatin based polyester urethane scaffold

    Indian Academy of Sciences (India)

    S Sarkar; A Chourasia; S Maji; S Sadhukhan; S Kumar; B Adhikari

    2006-10-01

    For tissue engineering purpose two gelatin based polyester urethane scaffolds of different compositions were prepared from lactic acid, polyethylene glycol 400 (PEG 400) and characterized by FTIR, XRD for their mechanical and morphological properties using SEM and optical microscopic analyses. Degradation and swelling studies of gelatin based polyester urethane scaffolds in phosphate buffer saline (PBS) were performed. Human keratinocyte cells were cultured within these scaffolds, which showed good cell adherence and proliferation.

  7. Metal-catalyzed simultaneous chain- and step-growth radical polymerization: marriage of vinyl polymers and polyesters.

    Science.gov (United States)

    Mizutani, Masato; Satoh, Kotaro; Kamigaito, Masami

    2010-06-02

    All polymerization reactions are categorized into two large different families, chain- and step-growth polymerizations, which are typically incompatible. Here, we report the simultaneous chain- and step-growth polymerization via the metal-catalyzed radical copolymerization of conjugated vinyl monomers and designed monomers possessing unconjugated C horizontal lineC and active C-Cl bonds. Especially, almost ideal linear random copolymers containing both vinyl polymer and polyester units in a single polymer chain were formed by the CuCl/1,1,4,7,10,10-hexamethyltriethylenetetramine- or RuCp*Cl(PPh(3))(2)-catalyzed copolymerization of methyl acrylate (MA) for the chain-growth polymerization and 3-butenyl 2-chloropropionate (1) for the step-growth polymerization. In contrast, other transition metal catalysts, such as CuCl with tris[2-(dimethylamino)ethyl]amine or N,N,N',N'',N''-pentamethyldiethylenetriamine and FeCl(2)/PnBu(3), resulted in branched structures via the concomitant chain-growth copolymerization of 1 with MA. The polymerization mechanism was studied in detail by NMR and MALDI-TOF-MS analyses of the polymerizations as well as the model reactions. Furthermore, a series of copolymers changing from random to multiblock polymer structures were obtained by varying the feed ratios of the two monomers. These copolymers can be easily degraded into lower molecular weight oligomers or polymers via methanolysis of the ester-linkages in the main chain using sodium carbonate.

  8. Rheological behaviour of nanocellulose reinforced unsaturated polyester nanocomposites.

    Science.gov (United States)

    Chirayil, Cintil Jose; Mathew, Lovely; Hassan, P A; Mozetic, Miran; Thomas, Sabu

    2014-08-01

    Nanocellulose (NC) reinforced unsaturated polyester (UPR) composites were prepared by mechanical mixing process. Effect of isora nanocellulose on the properties of polyester composites has been studied in detail. Rheological properties of unsaturated polyester resin suspensions containing various amounts (0.5, 1 and 3wt%) of nanocellulose were investigated by oscillatory rheometer with parallel plate geometry. Analysis of curing revealed that the time required for gelation in NC filled UPR is lower than neat resin, which describe the catalytic action of NC on cure reaction. NC reinforced polyester suspensions showed shear thinning behaviour initially and at higher shear rates they showed Newtonian behaviour. Tensile and impact properties showed superior behaviour revealing improved interfacial bonding between nanofiller and the polymer matrix. With respect to the neat polyester the percentage increase in tensile strength of 0.5wt% NC reinforced composite is 57%. Optical and atomic force microscopic studies confirmed that the dispersion state of NC within the polyester matrix was adequate. Maximum glass transition temperature is obtained for 0.5wt% NC reinforced composite, which showed an increase of 10°C than neat resin.

  9. A new approach to the synthesis of monomers and polymers incorporating furan/maleimide Diels-Alder adducts

    Science.gov (United States)

    Banella, Maria Barbara; Gioia, Claudio; Vannini, Micaela; Colonna, Martino; Celli, Annamaria; Gandini, Alessandro

    2016-05-01

    The Diels-Alder reaction between furan and maleimide moieties is a well-known and widely used strategy to build bio-based macromolecular structures with peculiar properties. The furan-maleimide adducts are thermally reversible because they can be broken above about 120°C and recombined at lower temperatures. At the moment only the monomers exhibiting the furan or the maleimide moieties on their extremity are used in order to get linear or cross-linked polymeric structures. The innovative idea described here consists in using a monomer bearing two carboxylic acidic groups on its extremities and a furan-maleimide Diels-Alder adduct within its structure. This monomer can give rise to classical polycondensation reactions leading to polymers. These polymers (which are polyesters in the present case) can be broken at high temperatures in correspondence of the furane-maleimide Diels-Alder adduct leading to segments exhibiting furan or maleimide moieties at their extremities, which at lower temperature recombine leading to random or block copolymers.

  10. Enzymatic Synthesis of Biobased Polyesters and Polyamides

    Directory of Open Access Journals (Sweden)

    Yi Jiang

    2016-06-01

    Full Text Available Nowadays, “green” is a hot topic almost everywhere, from retailers to universities to industries; and achieving a green status has become a universal aim. However, polymers are commonly considered not to be “green”, being associated with massive energy consumption and severe pollution problems (for example, the “Plastic Soup” as a public stereotype. To achieve green polymers, three elements should be entailed: (1 green raw materials, catalysts and solvents; (2 eco-friendly synthesis processes; and (3 sustainable polymers with a low carbon footprint, for example, (biodegradable polymers or polymers which can be recycled or disposed with a gentle environmental impact. By utilizing biobased monomers in enzymatic polymerizations, many advantageous green aspects can be fulfilled. For example, biobased monomers and enzyme catalysts are renewable materials that are derived from biomass feedstocks; enzymatic polymerizations are clean and energy saving processes; and no toxic residuals contaminate the final products. Therefore, synthesis of renewable polymers via enzymatic polymerizations of biobased monomers provides an opportunity for achieving green polymers and a future sustainable polymer industry, which will eventually play an essential role for realizing and maintaining a biobased and sustainable society.

  11. Photokopolimerisasi monomer akrilat degan kulit kras sapi

    Directory of Open Access Journals (Sweden)

    Dwi Wahini Nurhajati

    1997-06-01

    Full Text Available The research on photocopolymerization of acrylate monomer with cow crust hide had object to observe the resulted copolymer onto cow crust hide. Crust hides, saturated with aqueous emulsions containing 25 wt % of n-butyl acrylate (n-BA or tripropylene glycol diacrylate (TPGDA were irradiated by cobalt – 60 gamma rays with doses ranges from 5 to 25 kGy. The irradiated hides were washed with water, dried in air and extracted in soxhlet apparatus for 48 hours to remove homopolymer. The highest yield of photocopolymerization of n – butyl acrylate monomer with crust hides was found 17,7878% at dose 25 kGy, and for photocopolymerization of tripropylene glycol diacrylate with crust hides was found 39,4245% at dose 20 kGy.

  12. Functionalization of nanodiamond with epoxy monomer

    Institute of Scientific and Technical Information of China (English)

    Huan Huan Zhang; Ya Ting Liu; Rong Wang; Xiao Yan Yu; Xiong Wei Qu; Qing Xin Zhang

    2011-01-01

    A novel nanodiamond-epoxy derivative (ND-EP) was synthesized by grafting epoxy monomers onto the surface of nanodiamond (ND), and characterized by FTIR and TGA. The ratio of grafted epoxy groups was determined to be 32.5 wt% by TGA. The developed methodology provides an efficient method for the functionalization of nanodiamond material, which enables a variety of advanced engineering and biomedical applications of ND.

  13. Identification of acyltransferases required for cutin biosynthesis and production of cutin with suberin-like monomers.

    Science.gov (United States)

    Li, Yonghua; Beisson, Fred; Koo, Abraham J K; Molina, Isabel; Pollard, Mike; Ohlrogge, John

    2007-11-13

    Cutin and suberin are the two major lipid-based polymers of plants. Cutin is the structural polymer of the epidermal cuticle, the waterproof layer covering primary aerial organs and which is often the structure first encountered by phytopathogens. Suberin contributes to the control of diffusion of water and solutes across internal root tissues and in periderms. The enzymes responsible for assembly of the cutin polymer are largely unknown. We have identified two Arabidopsis acyltransferases essential for cutin biosynthesis, glycerol-3-phosphate acyltransferase (GPAT) 4 and GPAT8. Double knockouts gpat4/gpat8 were strongly reduced in cutin and were less resistant to desiccation and to infection by the fungus Alternaria brassicicola. They also showed striking defects in stomata structure including a lack of cuticular ledges between guard cells, highlighting the importance of cutin in stomatal biology. Overexpression of GPAT4 or GPAT8 in Arabidopsis increased the content of C16 and C18 cutin monomers in leaves and stems by 80%. In order to modify cutin composition, the acyltransferase GPAT5 and the cytochrome P450-dependent fatty acyl oxidase CYP86A1, two enzymes associated with suberin biosynthesis, were overexpressed. When both enzymes were overexpressed together the epidermal polyesters accumulated new C20 and C22 omega-hydroxyacids and alpha,omega-diacids typical of suberin, and the fine structure and water-barrier function of the cuticle were altered. These results identify GPATs as partners of fatty acyl oxidases in lipid polyester synthesis and indicate that their cooverexpression provides a strategy to probe the role of cutin composition and quantity in the function of plant cuticles.

  14. 21 CFR 888.4220 - Cement monomer vapor evacuator.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Cement monomer vapor evacuator. 888.4220 Section... (CONTINUED) MEDICAL DEVICES ORTHOPEDIC DEVICES Surgical Devices § 888.4220 Cement monomer vapor evacuator. (a) Identification. A cement monomer vapor evacuator is a device intended for use during surgery to contain or...

  15. 77 FR 54562 - Certain Polyester Staple Fiber From the Republic of Korea: Rescission of Antidumping Duty...

    Science.gov (United States)

    2012-09-05

    ...] Certain Polyester Staple Fiber From the Republic of Korea: Rescission of Antidumping Duty Administrative...'') initiated an administrative review of the antidumping duty order on certain polyester staple fiber from...

  16. SOLUTION RHEOLOGY OF HYPERBRANCHED POLYESTERS AND THEIR BLENDS WITH LINEAR POLYMERS

    Science.gov (United States)

    In this study, the rheological properties of different generations of hyperbranched polyesters in 1-methyl-2-pyrrolidinone solvent and their blends with poly(2-hydroxyethyl methacrylate) have ben investigated. All the hyperbranched polyester solutions exhibited Newtonian behavior...

  17. Mechanism and Effectiveness of Reduction Action of Unsaturated Polyester Resin Reducer

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The reduction action mechanism of unsaturated polyester resin reducer is analysed.The experimental results show that the active reducer bearing reactive functional group on the ends of molecules effectively lowers the curing shrinkage of unvaturated polyester resin.

  18. SOLUTION RHEOLOGY OF HYPERBRANCHED POLYESTERS AND THEIR BLENDS WITH LINEAR POLYMERS

    Science.gov (United States)

    In this study, the rheological properties of different generations of hyperbranched polyesters in 1-methyl-2-pyrrolidinone solvent and their blends with poly(2-hydroxyethyl methacrylate) have ben investigated. All the hyperbranched polyester solutions exhibited Newtonian behavior...

  19. 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

  20. SYNTHESIS OF A GROUP OF MESOGEN-JACKETED LIQUID CRYSTAL POLYMERS

    Institute of Scientific and Technical Information of China (English)

    ZHU Xinlong; YANG Qingchuan; ZHOU Qifeng

    1992-01-01

    A group of the mesogen jacketed liquid crystal polymers based on the monomers 2,5-bis (4-substituted benzoyl)oxystyrenes are synthesized. The substituents include alkoxy, alkyl, and cyano groups. The synthesis and the primary characterization of the liquid crystal phase of the monomers and the polymers are described. While some of the monomers give smectic textures the polymers are found to be nematic above their melting or glass transition temperatures. Interestingly the unsubstituted monomer and its polymer poly 2,5-di( benzoyloxy ) styrene are also liquid crystalline. The single crystal structure of one of the monomers is also discussed.

  1. Compression Properties of Polyester Needlepunched Fabric

    Directory of Open Access Journals (Sweden)

    Sanjoy Debnath, Ph.D.

    2009-12-01

    Full Text Available In the present paper, a study of the effects of fabricweight, fiber cross-sectional shapes (round, hollowand trilobal and presence of reinforcing materialon the compression properties (initial thickness,percentage compression, percentage thickness lossand percentage compression resilience of polyesterneedle punched industrial nonwoven fabrics ispresented. It was found that for fabrics with noreinforcing material, the initial thickness,compression, and thickness loss were higher thanfabrics with reinforcing material, irrespectiveoffiber cross-section. Compression resilience datashowed the reverse trend. Initial thickness fortrilobal cross-sectional fabric sample was highestfollowed by round and hollow cross-sectionedpolyester needle punched fabrics. The polyesterfabric made from hollow cross-sectioned fibersshowed the least percentage compression at everylevel of fabric weights. The trilobal cross-sectionedpolyester fabric sample showed higher thicknessloss followed by round and hollow cross-sectionedpolyester fabric samples respectively. The hollowcross-sectioned polyester fabric samples showedmaximum compression resilience followed byround and trilobal cross-sectioned polyestersamples irrespective of fabric weights. The initialthickness increases, but percentage compression,thickness loss and compression resilience decreaseswith the increase in fabric weight irrespective offiber cross-sectional shapes.

  2. Shock Wave Profiles in Glass Reinforced Polyester

    Science.gov (United States)

    Boteler, J. Michael; Rajendran, A. M.; Grove, David

    1999-06-01

    The promise of lightweight armor which is also structurally robust is of particular importance to the Army for future combat vehicles. Fiber reinforced organic matrix composites such as Glass Reinforced Polyester (GRP) are being considered for this purpose due to their lower density and promising dynamic response. The work discussed here extends the prior work of Boteler who studied the delamination strength of GRP and Dandekar and Beaulieu who investigated the compressive and tensile strengths of GRP. In a series of shock wave experiments, the wave profile was examined as a function of propagation distance in GRP. Uniaxial strain was achieved by plate impact in the ARL 102 mm bore single-stage light gas gun. Embedded polyvinylidene flouride (PVDF) stress-rate gauges provided a stress history at three unique locations in the GRP and particle velocity history was recorded with VISAR. The use of Lagrange gauges embedded in such a manner provides a means of calculating the constitutive relationships between specific volume, stress, and particle velocity uniquely with no prior assumptions of the form of constitutive relation. The Lagrangian analysis will be discussed and compared to Lagrangian hydrocode (EPIC) results employing a model to describe the viscoelastic response of the composite material in one-dimension.

  3. Biodegradation of Polyester Polyurethane by Endophytic Fungi▿

    Science.gov (United States)

    Russell, Jonathan R.; Huang, Jeffrey; Anand, Pria; Kucera, Kaury; Sandoval, Amanda G.; Dantzler, Kathleen W.; Hickman, DaShawn; Jee, Justin; Kimovec, Farrah M.; Koppstein, David; Marks, Daniel H.; Mittermiller, Paul A.; Núñez, Salvador Joel; Santiago, Marina; Townes, Maria A.; Vishnevetsky, Michael; Williams, Neely E.; Vargas, Mario Percy Núñez; Boulanger, Lori-Ann; Bascom-Slack, Carol; Strobel, Scott A.

    2011-01-01

    Bioremediation is an important approach to waste reduction that relies on biological processes to break down a variety of pollutants. This is made possible by the vast metabolic diversity of the microbial world. To explore this diversity for the breakdown of plastic, we screened several dozen endophytic fungi for their ability to degrade the synthetic polymer polyester polyurethane (PUR). Several organisms demonstrated the ability to efficiently degrade PUR in both solid and liquid suspensions. Particularly robust activity was observed among several isolates in the genus Pestalotiopsis, although it was not a universal feature of this genus. Two Pestalotiopsis microspora isolates were uniquely able to grow on PUR as the sole carbon source under both aerobic and anaerobic conditions. Molecular characterization of this activity suggests that a serine hydrolase is responsible for degradation of PUR. The broad distribution of activity observed and the unprecedented case of anaerobic growth using PUR as the sole carbon source suggest that endophytes are a promising source of biodiversity from which to screen for metabolic properties useful for bioremediation. PMID:21764951

  4. Aliphatic polyesters for medical imaging and theranostic applications.

    Science.gov (United States)

    Nottelet, Benjamin; Darcos, Vincent; Coudane, Jean

    2015-11-01

    Medical imaging is a cornerstone of modern medicine. In that context the development of innovative imaging systems combining biomaterials and contrast agents (CAs)/imaging probes (IPs) for improved diagnostic and theranostic applications focuses intense research efforts. In particular, the classical aliphatic (co)polyesters poly(lactide) (PLA), poly(lactide-co-glycolide) (PLGA) and poly(ɛ-caprolactone) (PCL), attract much attention due to their long track record in the medical field. This review aims therefore at providing a state-of-the-art of polyester-based imaging systems. In a first section a rapid description of the various imaging modalities, including magnetic resonance imaging (MRI), optical imaging, computed tomography (CT), ultrasound (US) and radionuclide imaging (SPECT, PET) will be given. Then, the two main strategies used to combine the CAs/IPs and the polyesters will be discussed. In more detail we will first present the strategies relying on CAs/IPs encapsulation in nanoparticles, micelles, dendrimers or capsules. We will then present chemical modifications of polyesters backbones and/or polyester surfaces to yield macromolecular imaging agents. Finally, opportunities offered by these innovative systems will be illustrated with some recent examples in the fields of cell labeling, diagnostic or theranostic applications and medical devices. Copyright © 2015 Elsevier B.V. All rights reserved.

  5. Study on the Synthesis and Biodegradation of Aliphatic Polyester

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    An aliphatic polyester, poly(hexalene adipate) (PHA) and an aliphatic copolyester, poly (hexalene adipate succinate) (PHAS) were synthesized by direct condensation of corresponding binary acid and binary alcohol in the presence of a catalyst, p-toluene sulfonic acid. The biodegradation of these polyesters were studied in the laboratory by enzyme attack and outdoor soil burial. The results show that these polyesters have good biodegradability and the copolyester PHAS, even displayed a better biodegradability than the polyester PHA. In the presence of Penicillium chrysogenum the weight loss reached 18.3% for the PHAS (film thickness 1.0 mm)and 9.1% for the PHA (film thickness 1.0 mm) after 28 days. Outdoor soil burial tests indicate that these polyesters also have good biodegradability in natural conditions. The weight loss reached 14.2% for PHAS (film thickness 0.1 mm) and 6.7% for PHA (film thickness 0.1mm) after burying in soil for 36 days.

  6. Interior microelectrolysis oxidation of polyester wastewater and its treatment technology.

    Science.gov (United States)

    Yang, Xiaoyi

    2009-09-30

    This paper has investigated the effects of interior microelectrolysis pretreatment on polyester wastewater treatment and analyzed its mechanism on COD and surfactant removal. The efficiency of interior microelectrolysis is mainly influenced by solution pH, aeration and reaction time. Contaminants can be removed not only by redox reaction and flocculation in the result of ferrous and ferric hydroxides but also by electrophoresis under electric fields created by electron flow. pH confirms the chemical states of surfactants, Fe(II)/Fe(III) ratio and the redox potential, and thus influences the effects of electrophoresis, flocculation and redox action on contaminant removal. Anaerobic and aerobic batch tests were performed to study the degradation of polyester wastewater. The results imply that interior microelectrolysis and anaerobic pretreatment are lacking of effectiveness if applied individually in treating polyester wastewater in spite of their individual advantages. The interior microelectrolysis-anaerobic-aerobic process was investigated to treat polyester wastewater with comparison with interior microelectrolysis-aerobic process and anaerobic-aerobic process. High COD removal efficiencies have been gotten by the combination of interior microelectrolysis with anaerobic technology and aerobic technology. The results also imply that only biological treatment was less effective in polyester wastewater treatment.

  7. Static and dynamical critical behavior of the monomer-monomer reaction model with desorption

    Science.gov (United States)

    da Costa, E. C.; Rusch, Flávio Roberto

    2016-06-01

    We studied in this work the monomer-monomer reaction model on a linear chain. The model is described by the following reaction: A + B → AB, where A and B are two monomers that arrive at the surface with probabilities yA and yB, respectively, and we have considered desorption of the monomer B with probability α. The model is studied in the adsorption controlled limit where the reaction rate is infinitely larger than the adsorption rate. We employ site and pair mean-field approximations as well as static and dynamical Monte Carlo simulations. We show that the model exhibits a continuous phase transition between an active steady state and an A-absorbing state, when the parameter yA is varied through a critical value, which depends on the value of α. Monte Carlo simulations and finite-size scaling analysis near the critical point are used to determine the static critical exponents β and ν⊥ and the dynamical critical exponents ν∥ and z. The results found for the monomer-monomer reaction model with B desorption, in the linear chain, are different from those found by E. V. Albano (Albano, 1992) and are in accordance with the values obtained by Jun Zhuo and Sidney Redner (Zhuo and Redner, 1993), and endorse the conjecture of Grassberger, which states that any system undergoing a continuous phase transition from an active steady state to a single absorbing state, exhibits the same critical behavior of the directed percolation universality class.

  8. 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

  9. 77 FR 19619 - Certain Polyester Staple Fiber from the People's Republic of China: Extension of Preliminary...

    Science.gov (United States)

    2012-04-02

    ... International Trade Administration Certain Polyester Staple Fiber from the People's Republic of China: Extension... polyester staple fiber from the People's Republic of China (``PRC''). This review covers the period June 1... administrative review of the antidumping duty order on certain polyester staple fiber from the PRC.\\1\\...

  10. 75 FR 47795 - Certain Polyester Staple Fiber from Korea: Rescission of Antidumping Duty Administrative Review

    Science.gov (United States)

    2010-08-09

    ... International Trade Administration Certain Polyester Staple Fiber from Korea: Rescission of Antidumping Duty... (June 30, 2010). Scope of the Order Polyester staple fiber (``PSF'') covered by the scope of the order... polyesters measuring 3.3 decitex (3 denier, inclusive) or more in diameter. This merchandise is cut...

  11. 75 FR 6352 - Certain Polyester Staple Fiber from the People's Republic of China: Extension of Preliminary...

    Science.gov (United States)

    2010-02-09

    ... International Trade Administration Certain Polyester Staple Fiber from the People's Republic of China: Extension... polyester staple fiber from the People's Republic of China (``PRC''). This review covers the period June 1... duty order on certain polyester staple fiber from the PRC. See Initiation of Antidumping...

  12. 76 FR 7532 - Certain Polyester Staple Fiber From the People's Republic of China: Extension of Preliminary...

    Science.gov (United States)

    2011-02-10

    ... International Trade Administration Certain Polyester Staple Fiber From the People's Republic of China: Extension... polyester staple fiber from the People's Republic of China (``PRC''). This review covers the period June 1... duty order on certain polyester staple fiber from the PRC. See Initiation of Antidumping...

  13. 75 FR 30373 - Certain Polyester Staple Fiber From the People's Republic of China: Extension of Preliminary...

    Science.gov (United States)

    2010-06-01

    ... International Trade Administration Certain Polyester Staple Fiber From the People's Republic of China: Extension... polyester staple fiber from the People's Republic of China (``PRC''). This review covers the period June 1... polyester staple fiber from the PRC. See Initiation of Antidumping and Countervailing Duty...

  14. 75 FR 39208 - Polyester Staple Fiber from Taiwan: Final Results of Changed-Circumstances Antidumping Duty...

    Science.gov (United States)

    2010-07-08

    ... International Trade Administration Polyester Staple Fiber from Taiwan: Final Results of Changed- Circumstances... antidumping duty order on polyester staple fiber from Taiwan. DATES: Effective Date: July 8, 2010. FOR FURTHER... changed-circumstances review of the antidumping duty order on polyester staple fiber from Taiwan...

  15. 76 FR 11268 - Certain Polyester Staple Fiber From Korea and Taiwan

    Science.gov (United States)

    2011-03-01

    ... COMMISSION Certain Polyester Staple Fiber From Korea and Taiwan AGENCY: United States International Trade Commission. ACTION: Institution five-year reviews concerning the antidumping duty orders on certain polyester... whether revocation of the antidumping duty orders on certain polyester staple fiber from Korea and...

  16. 77 FR 54561 - Certain Polyester Staple Fiber From Taiwan: Final Results of Antidumping Duty Administrative Review

    Science.gov (United States)

    2012-09-05

    ...] Certain Polyester Staple Fiber From Taiwan: Final Results of Antidumping Duty Administrative Review AGENCY... antidumping duty order on certain polyester staple fiber from Taiwan. The period of review is May 1, 2010... administrative review of the antidumping duty order on certain polyester staple fiber from Taiwan. See...

  17. 75 FR 4044 - Polyester Staple Fiber From Taiwan: Initiation and Preliminary Results of Changed-Circumstances...

    Science.gov (United States)

    2010-01-26

    ... International Trade Administration Polyester Staple Fiber From Taiwan: Initiation and Preliminary Results of... antidumping duty order on polyester staple fiber from Taiwan. We have preliminarily concluded that Far Eastern... the antidumping duty order on polyester staple fiber from Taiwan. Interested parties are invited...

  18. 75 FR 51442 - Polyester Staple Fiber from Taiwan: Rescission of Antidumping Duty Administrative Review in Part

    Science.gov (United States)

    2010-08-20

    ... International Trade Administration Polyester Staple Fiber from Taiwan: Rescission of Antidumping Duty... Commerce initiated an administrative review of the antidumping duty order on polyester staple fiber from...) initiated an ] administrative review of the antidumping duty order on polyester staple fiber from...

  19. 78 FR 17637 - Polyester Staple Fiber From Taiwan: Preliminary Results of Antidumping Duty Administrative Review...

    Science.gov (United States)

    2013-03-22

    ... International Trade Administration Polyester Staple Fiber From Taiwan: Preliminary Results of Antidumping Duty... the antidumping duty order on polyester staple fiber (PSF) from Taiwan. The period of review (POR) is... Antidumping Duty Administrative Review: Polyester Staple Fiber from Taiwan'' dated concurrently with...

  20. 78 FR 14512 - Certain Polyester Staple Fiber From the People's Republic of China: Preliminary Results and...

    Science.gov (United States)

    2013-03-06

    ... International Trade Administration Certain Polyester Staple Fiber From the People's Republic of China... order on certain polyester staple fiber from the People's Republic of China (``PRC''). The period of... Sichuan Chemical Fiber Corp. and Huvis Sichuan Polyester Fiber Ltd. (``Huvis Sichuan'') are part of...

  1. 77 FR 6783 - Certain Polyester Staple Fiber From the People's Republic of China: Extension of Preliminary...

    Science.gov (United States)

    2012-02-09

    ... International Trade Administration Certain Polyester Staple Fiber From the People's Republic of China: Extension... polyester staple fiber from the People's Republic of China (``PRC''). This review covers the period June 1... administrative review of the antidumping duty order on certain polyester staple fiber from the PRC....

  2. 77 FR 62217 - Certain Polyester Staple Fiber From the People's Republic of China: Continuation of Antidumping...

    Science.gov (United States)

    2012-10-12

    ... Polyester Staple Fiber From the People's Republic of China: Continuation of Antidumping Duty Order AGENCY... certain polyester staple fiber from the People's Republic of China (``PRC'') would likely lead to a... the sunset review of the antidumping duty order on certain polyester staple fiber from the...

  3. 76 FR 58040 - Certain Polyester Staple Fiber From Korea and Taiwan

    Science.gov (United States)

    2011-09-19

    ... COMMISSION Certain Polyester Staple Fiber From Korea and Taiwan Determination On the basis of the record \\1... antidumping duty orders on certain polyester staple fiber from Korea and Taiwan would be likely to lead to...), entitled Certain Polyester Staple Fiber From Korea and Taiwan: Investigation Nos. 731-TA-825 and...

  4. 78 FR 38938 - Polyester Staple Fiber From Taiwan: Final Results of Antidumping Duty Administrative Review; 2011...

    Science.gov (United States)

    2013-06-28

    ... International Trade Administration Polyester Staple Fiber From Taiwan: Final Results of Antidumping Duty... results of the administrative review of the antidumping duty order on polyester staple fiber (PSF) from... Preliminary Results. None were received. \\1\\ See Polyester Staple Fiber From Taiwan: Preliminary Results...

  5. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Partial phosphoric acid esters of polyester resins... COMPONENTS OF COATINGS Substances for Use as Components of Coatings § 175.260 Partial phosphoric acid esters of polyester resins. Partial phosphoric acid esters of polyester resins identified in this section...

  6. Research on Electroless Silver Conductive Polyester Fabric%化学镀银导电涤纶织物的研究

    Institute of Scientific and Technical Information of China (English)

    董猛; 田俊莹; 江红

    2016-01-01

    Conductive polyester fabric was prepared by electroless silver plating with glucose as a reducing a-gent.The effects of concentration of silver nitrate, glucose concentration, ethanol concentration and reaction time on the conductive properties of polyester fabric were studied.The surface morphology and crystal structure of the silver coating were investigated by SEM and XRD.And electromagnetic shielding performance was also tested. The results showed that electroless silver plating polyester fabric had excellent electrical conductivity and electro-magnetic shielding performance of polyester fabric was remarkably improved by electroless silver plating.%以葡萄糖为还原剂,采用化学镀银法制备导电涤纶织物,研究了硝酸银浓度、葡萄糖浓度、乙醇浓度及反应时间对涤纶织物导电性能的影响,通过SEM和XRD图谱分析导电织物表面形貌与晶体结构,并测试其电磁屏蔽性能。结果表明,化学镀银涤纶织物具有优异的导电性能,且化学镀银后涤纶织物的电磁屏蔽性能明显增加。

  7. Probing the potential of polyester for CO₂ capture.

    Science.gov (United States)

    Zulfiqar, Sonia; Sarwar, Muhammad Ilyas

    2014-07-01

    Global warming, the major environmental issue confronted by humanity today, is caused by rising level of green house gases. Carbon capture and storage technologies offer potential for tapering CO₂ emission in the atmosphere. Adsorption is believed to be a promising technology for CO₂ capture. For this purpose, a polyester was synthesized by polycondensation of 1,3,5-benzenetricarbonyl trichloride and cyanuric acid in pyridine and dichloromethane mixture. The polymer was then characterized using FT-IR, TGA, BET surface area and pore size analysis, FESEM and CO₂ adsorption measurements. The CO₂ adsorption capacities of the polyester were evaluated at a pressure of 1bar and two different temperatures (273 and 298K). The performance of these materials to adsorb CO₂ at atmospheric pressure was measured by optimum CO₂ uptake of 0.244 mmol/g at 273K. The synthesized polyester, therefore, has the potential to be exploited as CO₂ adsorbent in pre-combustion capture process.

  8. Biodegradation of polyester polyurethane by Aspergillus tubingensis.

    Science.gov (United States)

    Khan, Sehroon; Nadir, Sadia; Shah, Zia Ullah; Shah, Aamer Ali; Karunarathna, Samantha C; Xu, Jianchu; Khan, Afsar; Munir, Shahzad; Hasan, Fariha

    2017-03-15

    The xenobiotic nature and lack of degradability of polymeric materials has resulted in vast levels of environmental pollution and numerous health hazards. Different strategies have been developed and still more research is being in progress to reduce the impact of these polymeric materials. This work aimed to isolate and characterize polyester polyurethane (PU) degrading fungi from the soil of a general city waste disposal site in Islamabad, Pakistan. A novel PU degrading fungus was isolated from soil and identified as Aspergillus tubingensis on the basis of colony morphology, macro- and micro-morphology, molecular and phylogenetic analyses. The PU degrading ability of the fungus was tested in three different ways in the presence of 2% glucose: (a) on SDA agar plate, (b) in liquid MSM, and (c) after burial in soil. Our results indicated that this strain of A. tubingensis was capable of degrading PU. Using scanning electron microscopy (SEM), we were able to visually confirm that the mycelium of A. tubingensis colonized the PU material, causing surface degradation and scarring. The formation or breakage of chemical bonds during the biodegradation process of PU was confirmed using Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR) spectroscopy. The biodegradation of PU was higher when plate culture method was employed, followed by the liquid culture method and soil burial technique. Notably, after two months in liquid medium, the PU film was totally degraded into smaller pieces. Based on a comprehensive literature search, it can be stated that this is the first report showing A. tubingensis capable of degrading PU. This work provides insight into the role of A. tubingensis towards solving the dilemma of PU wastes through biodegradation.

  9. Tandem synthesis of alternating polyesters from renewable resources.

    Science.gov (United States)

    Robert, Carine; de Montigny, Frédéric; Thomas, Christophe M

    2011-12-13

    The vast majority of commodity materials are obtained from petrochemical feedstocks. These resources will plausibly be depleted within the next 100 years, and the peak in global oil production is estimated to occur within the next few decades. In this regard, biomass represents an abundant carbon-neutral renewable resource for the production of polymers. Here we report a new strategy, based on tandem catalysis, to obtain renewable materials. Commercially available complexes are found to be efficient catalysts for alternating polyesters from the cyclization of dicarboxylic acids followed by alternating copolymerization of the resulting anhydrides with epoxides. This operationally simple method is an attractive strategy for the production of new biodegradable polyesters.

  10. Copolymerization of Carbon–carbon Double-bond Monomer (Styrene with Cyclic Monomer (Tetrahydrofuran

    Directory of Open Access Journals (Sweden)

    Sari Fouad

    2012-12-01

    Full Text Available We reported in this work that the cationic copolymerization in one step takes place between carbon–carbon double-bond monomer styrene with cyclic monomer tetrahydrofuran. The comonomers studied belong to different families: vinylic and cyclic ether. The reaction is initiated with maghnite-H+ an acid exchanged montmorillonite as acid solid ecocatalyst. Maghnite-H+ is already used as catalyst for polymerization of many vinylic and heterocyclic monomers. The oxonium ion of tetrahydrofuran and carbonium ion of styrene propagated the reaction of copolymerization. The acetic anhydride is essential for the maintenance of the ring opening of tetrahydrofuran and the entry in copolymerization. The temperature was kept constant at 40°C in oil bath heating for 6 hours. A typical reaction product was analyzed by 1H-NMR, 13C-NMR and IR and the formation of the copolymer was confirmed. The reaction was proved by matched with analysis. The maghnite-H+ allowed us to obtain extremely pure copolymer in good yield by following a simples operational conditions. Copyright © 2012 by BCREC UNDIP. All rights reservedReceived: 29th October 2012; Revised: 29th November 2012; Accepted: 29th November 2012[How to Cite: S. Fouad, M.I. Ferrahi, M. Belbachir. (2012. Copolymerization of Carbon–carbon Double-bond Monomer (Styrene with Cyclic Monomer (Tetrahydrofuran. Bulletin of Chemical Reaction Engineering & Catalysis, 7(2: 165-171. (doi:10.9767/bcrec.7.2.4074.165-171][How to Link / DOI: http://dx.doi.org/10.9767/bcrec.7.2.4074.165-171 ] | View in 

  11. Development of Photocrosslinkable Urethane-Doped Polyester Elastomers for Soft Tissue Engineering.

    Science.gov (United States)

    Zhang, Yi; Tran, Richard T; Gyawali, Dipendra; Yang, Jian

    2011-01-01

    Finding an ideal biomaterial with the proper mechanical properties and biocompatibility has been of intense focus in the field of soft tissue engineering. This paper reports on the synthesis and characterization of a novel crosslinked urethane-doped polyester elastomer (CUPOMC), which was synthesized by reacting a previously developed photocrosslinkable poly (octamethylene maleate citrate) (POMC) prepolymers (pre-POMC) with 1,6-hexamethylene diisocyanate (HDI) followed by thermo- or photo-crosslinking polymerization. The mechanical properties of the CUPOMCs can be tuned by controlling the molar ratios of pre-POMC monomers, and the ratio between the prepolymer and HDI. CUPOMCs can be crosslinked into a 3D network through polycondensation or free radical polymerization reactions. The tensile strength and elongation at break of CUPOMC synthesized under the known conditions range from 0.73±0.12MPa to 10.91±0.64MPa and from 72.91±9.09% to 300.41±21.99% respectively. Preliminary biocompatibility tests demonstrated that CUPOMCs support cell adhesion and proliferation. Unlike the pre-polymers of other crosslinked elastomers, CUPOMC pre-polymers possess great processability demonstrated by scaffold fabrication via a thermally induced phase separation method. The dual crosslinking methods for CUPOMC pre-polymers should enhance the versatile processability of the CUPOMC used in various conditions. Development of CUPOMC should expand the choices of available biodegradable elastomers for various biomedical applications such as soft tissue engineering.

  12. Study on the control of the compositions and properties of a biodegradable polyester elastomer

    Energy Technology Data Exchange (ETDEWEB)

    Liu Quanyong; Weng Jingyi; Zhang Liqun [Key Laboratory of Beijing City on Preparation and Processing of Novel Polymer Materials, Beijing University of Chemical Technology, Beijing 100029 (China); Tan Tianwei, E-mail: liu_quanyong@126.co, E-mail: zhanglq@mail.buct.edu.c [Key Laboratory of Bioprocess of Beijing, Beijing University of Chemical Technology, Beijing 100029 (China)

    2009-04-15

    Biodegradable polyester elastomers are widely reported to be applied in varied biomedical fields. In this paper, we attempt to investigate how both the thermal-curing time and molar ratio of the monomers affect the final compositions and properties of the novel poly(glycerol-sebacate-citrate) (PGSC) elastomers. First, PGSC elastomers are obtained after the thermal curing of the moldable mixtures consisting of citric acid and poly(glycerol-sebacate) (PGS) prepolymers synthesized in the lab. Then further studies show that, on the one hand, the control of longer thermal-curing time results in elastomers with less sol, lower swelling degree, slower degradation, greater mechanical strength and higher glass transition temperature and, on the other hand, the crosslink with more citric acid is advantageous to greatly improving their mechanical strength and glass transition temperatures, simultaneously decreasing their sol contents, swelling degrees and degradation rates. The PGSC elastomers show thermosetting properties, certain strength, mass losses lower than 20% after 4-week degradation and durative water absorption during degradation. Thus they might be potentially used as degradable bio-coatings, varied soft biomedical membranes and drug delivery matrices.

  13. Study on the control of the compositions and properties of a biodegradable polyester elastomer.

    Science.gov (United States)

    Liu, Quanyong; Tan, Tianwei; Weng, Jingyi; Zhang, Liqun

    2009-04-01

    Biodegradable polyester elastomers are widely reported to be applied in varied biomedical fields. In this paper, we attempt to investigate how both the thermal-curing time and molar ratio of the monomers affect the final compositions and properties of the novel poly(glycerol-sebacate-citrate) (PGSC) elastomers. First, PGSC elastomers are obtained after the thermal curing of the moldable mixtures consisting of citric acid and poly(glycerol-sebacate) (PGS) prepolymers synthesized in the lab. Then further studies show that, on the one hand, the control of longer thermal-curing time results in elastomers with less sol, lower swelling degree, slower degradation, greater mechanical strength and higher glass transition temperature and, on the other hand, the crosslink with more citric acid is advantageous to greatly improving their mechanical strength and glass transition temperatures, simultaneously decreasing their sol contents, swelling degrees and degradation rates. The PGSC elastomers show thermosetting properties, certain strength, mass losses lower than 20% after 4-week degradation and durative water absorption during degradation. Thus they might be potentially used as degradable bio-coatings, varied soft biomedical membranes and drug delivery matrices.

  14. Degradation of polyester polyurethane by a newly isolated soil bacterium, Bacillus subtilis strain MZA-75.

    Science.gov (United States)

    Shah, Ziaullah; Krumholz, Lee; Aktas, Deniz Fulya; Hasan, Fariha; Khattak, Mutiullah; Shah, Aamer Ali

    2013-11-01

    A polyurethane (PU) degrading bacterial strain MZA-75 was isolated from soil through enrichment technique. The bacterium was identified through 16S rRNA gene sequencing, the phylogenetic analysis indicated the strain MZA-75 belonged to genus Bacillus having maximum similarity with Bacillus subtilis strain JBE0016. The degradation of PU films by strain MZA-75 in mineral salt medium (MSM) was analyzed by scanning electron microscopy (SEM), fourier transform infra-red spectroscopy (FT-IR) and gel permeation chromatography (GPC). SEM revealed the appearance of widespread cracks on the surface. FTIR spectrum showed decrease in ester functional group. Increase in polydispersity index was observed in GPC, which indicates chain scission as a result of microbial treatment. CO2 evolution and cell growth increased when PU was used as carbon source in MSM in Sturm test. Increase in both cell associated and extracellular esterases was observed in the presence of PU indicated by p-Nitrophenyl acetate (pNPA) hydrolysis assay. Analysis of cell free supernatant by gas chromatography-mass spectrometry (GC-MS) revealed that 1,4-butanediol and adipic acid monomers were produced. Bacillus subtilis strain MZA-75 can degrade the soft segment of polyester polyurethane, unfortunately no information about the fate of hard segment could be obtained. Growth of strain MZA-75 in the presence of these metabolites indicated mineralization of ester hydrolysis products into CO2 and H2O.

  15. Development of novel electrically conductive scaffold based on hyperbranched polyester and polythiophene for tissue engineering applications.

    Science.gov (United States)

    Jaymand, Mehdi; Sarvari, Raana; Abbaszadeh, Parisa; Massoumi, Bakhshali; Eskandani, Morteza; Beygi-Khosrowshahi, Younes

    2016-11-01

    A novel electrically conductive scaffold containing hyperbranched aliphatic polyester (HAP), polythiophene (PTh), and poly(ε-caprolactone) (PCL) for regenerative medicine application was succesfully fabricated via electrospinning technique. For this purpose, the HAP (G4; fourth generation) was synthesized via melt polycondensation reaction from tris(methylol)propane and 2,2-bis(methylol)propionic acid (bis-MPA). Afterward, the synthesized HAP was functionalized with 2-thiopheneacetic acid in the presence of N,N-dicyclohexyl carbodiimide, and N-hydroxysuccinimide as coupling agent and catalyst, respectively, to afford a thiophene-functionalized G4 macromonomer. This macromonomer was subsequently used in chemical oxidation copolymerization with thiophene monomer to produce a star-shaped PTh with G4 core (G4-PTh). The solution of the G4-PTh, and PCL was electrospun to produce uniform, conductive, and biocompatible nanofibers. The conductivity, hydrophilicity, and mechanical properties of these nanofibers were investigated. The biocompatibility of the electrospun nanofibers were evaluated by assessing the adhesion and proliferation of mouse osteoblast MC3T3-E1 cell line and in vitro degradability to demonstrate their potential uses as a tissue engineering scaffold. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 2673-2684, 2016.

  16. Research on Influence Factors of Surfactivity of Polyester Polyether Block Copolymer

    Institute of Scientific and Technical Information of China (English)

    WU Ming-hua; LIN He-ming

    2008-01-01

    Polyester polyether block copolymer (PPBC) was synthesized by ester-exchange and polycodensation reactions using dimethyl terephthalate (DMT), ethylene glycol (EG) and polyethylene glycol (PEG) as monomer. The effects of PEG molecular weight, mol ratio of DMT to PEG (nDMT/nPEG), temperature and time of polycondensation reaction and vacuum degree in the reaction system on the surface tension and critical micelle concentration (CMC) of PPBC aqueous solution were studied. It was found that both the molecular weight and the concentration of PEG can affect PPBC'S surface activity obviously, and the optimum synthesis condition of PPBC used as surfactant is as follows: PEG molecular weight is 1500, mol ratio of DMT to PEG is 3, temperature and time of polycondensation reaction is 260°C×1h, vacuum degree of condensation reaction is 0.03-0.05 MPa. It was proved by surface tension measurement of PPBC aqueous solution that the PPBC synthesized in this condition is a good surfactant with excellent surfactivity.

  17. Synthesis of Unsaturated Polyester Resins from Various Bio-Derived Platform Molecules

    Directory of Open Access Journals (Sweden)

    Thomas J. Farmer

    2015-07-01

    Full Text Available Utilisation of bio-derived platform molecules in polymer synthesis has advantages which are, broadly, twofold; to digress from crude oil dependence of the polymer industry and secondly to reduce the environmental impact of the polymer synthesis through the inherent functionality of the bio-derived platform molecules. Bulk polymerisation of bio-derived unsaturated di-acids has been employed to produce unsaturated polyester (UPEs which have been analysed by GPC, TGA, DSC and NMR spectroscopy, advancing on the analysis previously reported. UPEs from the diesters of itaconic, succinic, and fumaric acids were successfully synthesised with various diols and polyols to afford resins of MN 480–477,000 and Tg of −30.1 to −16.6 °C with solubilities differing based on starting monomers. This range of properties allows for many applications and importantly due to the surviving Michael acceptor moieties, solubility and cross-linking can be specifically tailored, post polymerisation, to the desired function. An improved synthesis of itaconate and succinate co-polymers, via the initial formation of an itaconate bis-diol, is also demonstrated for the first time, resulting in significantly improved itaconate incorporation.

  18. The catalytic microwave synthesis of biodegradable polyester polyols based on castor oil and l-lactide

    Science.gov (United States)

    Kojić, D.; Erceg, T.; Vukić, N.; Teofilović, V.; Ristić, I.; Budinski-Simendić, J.; Aleksić, V.

    2017-01-01

    Various strategies for achieving a functional poly(lactic acid) (PLA) have been developed such as ring-opening copolymerization with a functional monomer, the use of functional initiator and various post polymerization modifications. It is possible to obtain the star shaped polymer using natural oil with at least three OH groups as an initiator. It was estimated that despite of low-molecular mass of star-shaped PLA, the hydrophobic castor oil central core influenced the slow degradation rate in the case of injectable biomedical application. The star-shaped polymers with low-molecular-mass have a lower melt viscosity correlated with linear counterparts. In soft tissue reparation the polymer viscosity increases with fluid body contact and the solid implant can be formed. To ensure liquid state at injection temperature the low molar mass polymer is favorable. There is a particular size for each macromolecular chains at which chain entanglement occurs. In this work the influence of the l-lactide (LA) and the castor oil (CO) contents on the size of biodegradable branched polyester polyols was studied. The average molecular masses of synthesized polymers were estimated by GPC procedure. In sample formulations the [LA]/[CO] ratios were from to 113 to 533. Mn values for obtained polymers were from 5000 to 20000 Da. The molecular mass distribution for the resulting polymers was between 1.09 and 1.37.

  19. Evaluation of biodegradable polyester-co-lactone microparticles for protein delivery.

    Science.gov (United States)

    Tawfeek, Hesham M; Khidr, Sayed H; Samy, Eman M; Ahmed, Sayed M; Gaskell, Elsie E; Hutcheon, Gillian A

    2014-09-01

    Abstract Poly(glycerol adipate-co-ω-pentadecalactone) (PGA-co-PDL) was previously evaluated for the colloidal delivery of α-chymotrypsin. In this article, the effect of varying polymer molecular weight (MW) and chemistry on particle size and morphology; encapsulation efficiency; in vitro release; and the biological activity of α-chymotrypsin (α-CH) and lysozyme (LS) were investigated. Microparticles were prepared using emulsion solvent evaporation and evaluated by various methods. Altering the MW or monomer ratio of PGA-co-PDL did not significantly affect the encapsulation efficiency and overall poly(1,3-propanediol adipate-co-ω-pentadecalactone) (PPA-co-PDL) demonstrated the highest encapsulation efficiency. In vitro release varied between polymers, and the burst release for α-CH-loaded microparticles was lower when a higher MW PGA-co-PDL or more hydrophobic PPA-co-PDL was used. The results suggest that, although these co-polyesters could be useful for protein delivery, little difference was observed between the different PGA-co-PDL polymers and PPA-co-PDL generally provided a higher encapsulation and slower release of enzyme than the other polymers tested.

  20. Corrosion Protection Performance of Polyester-Melamine Coating with Natural Wood Fiber Using EIS Analysis

    Energy Technology Data Exchange (ETDEWEB)

    Shin, PyongHwa; Shon, MinYoung [Pukyong National University, Busan (Korea, Republic of); Jo, DuHwan [POSCO, Gwangyang (Korea, Republic of)

    2016-04-15

    In the present study, polyester-melamine coating systems with natural wood fiber (NWF) were prepared and the effects of NWF on the corrosion protectiveness of the polyester-melamine coating were examined using EIS analysis. From the results, higher average surface roughness was observed with increase of NWF content. Water diffusivity and water uptake into the polyester-melamine coatings with NWF were much higher than that into the pure polyester-melamine coating. The decrease in the impedance modulus |Z| was associated with the localized corrosion on carbon steel, confirming that corrosion protection of the polyester-melamine coatings with NWF well agrees with its water transport behavior.

  1. Structural Analysis of Aromatic Liquid Crystalline Polyesters

    Directory of Open Access Journals (Sweden)

    Arpad Somogyi

    2011-01-01

    Full Text Available Laboratory preparations of liquid crystalline prepolymers, distillates accompanying prepolymers, final polymers, and sublimates accompanying final polymers were examined. NaOD/D2O depolymerization of prepolymers and polymers back to monomers with integration of the 1H NMR spectra showed up to 6% excess of carboxyls over phenol groups, caused partly by loss of the low-boiling comonomer hydroquinone through distillation during prepolymerization and leaving anhydride units in the polymer chain. ESI− MS and MS/MS of hexafluoroisopropanol extracts of the prepolymer detected small molecules including some containing anhydride groups; ESI+ MS showed the presence of small cyclic oligomers. 1H NMR (including TOCSY spectra provided more quantitative analyses of these oligomers. The final polymerization increases the length of the polymer chains and sublimes out the small oligomers. Anhydride linkages remaining in the polymer must make LCP’s more susceptible to degradation by nucleophilic reagents such as water, alkalis, and amines.

  2. Laparoscopic-assisted Ventral Hernia Repair: Primary Fascial Repair with Polyester Mesh versus Polyester Mesh Alone.

    Science.gov (United States)

    Karipineni, Farah; Joshi, Priya; Parsikia, Afshin; Dhir, Teena; Joshi, Amit R T

    2016-03-01

    Laparoscopic-assisted ventral hernia repair (LAVHR) with mesh is well established as the preferred technique for hernia repair. We sought to determine whether primary fascial closure and/or overlap of the mesh reduced recurrence and/or complications. We conducted a retrospective review on 57 LAVHR patients using polyester composite mesh between August 2010 and July 2013. They were divided into mesh-only (nonclosure) and primary fascial closure with mesh (closure) groups. Patient demographics, prior surgical history, mesh overlap, complications, and recurrence rates were compared. Thirty-nine (68%) of 57 patients were in the closure group and 18 (32%) in the nonclosure group. Mean defect sizes were 15.5 and 22.5 cm(2), respectively. Participants were followed for a mean of 1.3 years [standard deviation (SD) = 0.7]. Recurrence rates were 2/39 (5.1%) in the closure group and 1/18 (5.6%) in the nonclosure group (P = 0.947). There were no major postoperative complications in the nonclosure group. The closure group experienced four (10.3%) complications. This was not a statistically significant difference (P = 0.159). The median mesh-to-hernia ratio for all repairs was 15.2 (surface area) and 3.9 (diameter). Median length of stay was 14.5 hours (1.7-99.3) for patients with nonclosure and 11.9 hours (6.9-90.3 hours) for patients with closure (P = 0.625). In conclusion, this is one of the largest series of LAVHR exclusively using polyester dual-sided mesh. Our recurrence rate was about 5 per cent. Significant mesh overlap is needed to achieve such low recurrence rates. Primary closure of hernias seems less important than adequate mesh overlap in preventing recurrence after LAVHR.

  3. 全消光阻燃聚酯切片工业制造及性能表征%Study on Synthesis and Properties of Dull Flame-Retardant Polyester

    Institute of Scientific and Technical Information of China (English)

    陆慧良

    2012-01-01

    采用2-羧乙基苯基次磷酸(CEPPA)、[(6-氧(6H)-二苯并(c,e) (1,2)-氧磷杂己环-6-酮)甲基]-丁二酸(DDP),在连续化聚酯装置上工业化生产全消光阻燃聚酯切片.介绍了全消光阻燃聚酯切片的生产过程,并对产品性能进行了表征.结果表明:生产过程稳定,产品质量优异,全消光阻燃聚酯切片的结晶性能低于常规全消光切片,热稳定性能优于常规全消光切片,阻燃性能优良.%The phosphorus -containing flame -retardant polyesters from CEPPA and DDP in continuous polyester unit were produced. The production process of phosphorus-containing flame-retardant polyester and it's product properties were introduced. The results showed that the production process was steady and product quality was excellent. As compared with regular dull PET, the synthesized phosphorus-containing flame-retardant polyester had lower crystallization capacity, and better thermal stability. The synthesized phosphorus-containing flame-retardant polyester had excellent flame-retardant property.

  4. Synthesis and photoactivity of phenylazonaphthalene peptide nucleic acid monomers

    Institute of Scientific and Technical Information of China (English)

    Jin Du Li; Miao Chen; Sheng Liu; Hao Bo Zhang; Zhi Lu Liu

    2008-01-01

    Phenylazonaphthalene peptide nucleic acid (PNA) monomers were successfully synthesized,and their photoisomerization was examined.The new PNA monomers showed reversible trans-cis isomerization with UV and visible light irradiation,which might be the foundation of photo-regulating the hybridization between PNA containing phenylazonaphthalene unit and DNA.Simultaneously,the fluorescence of the new PNA monomers might make them especially useful as structural probes.

  5. Computational screening of oxetane monomers for novel hydroxy terminated polyethers.

    Science.gov (United States)

    Sarangapani, Radhakrishnan; Ghule, Vikas D; Sikder, Arun K

    2014-06-01

    Energetic hydroxy terminated polyether prepolymers find paramount importance in search of energetic binders for propellant applications. In the present study, density functional theory (DFT) has been employed to screen the various novel energetic oxetane derivatives, which usually construct the backbone for these energetic polymers. Molecular structures were investigated at the B3LYP/6-31G* level, and isodesmic reactions were designed for calculating the gas phase heats of formation. The condensed phase heats of formation for designed compounds were calculated by the Politzer approach using heats of sublimation. Among the designed oxetane derivatives, T4 and T5 possess condensed phase heat of formation above 210 kJ mol(-1). The crystal packing density of the designed oxetane derivatives varied from 1.2 to 1.6 g/cm(3). The detonation velocities and pressures were evaluated using the Kamlet-Jacobs equations, utilizing the predicted densities and HOFCond. It was found that most of the designed oxetane derivatives have detonation performance comparable to the monomers of benchmark energetic polymers viz., NIMMO, AMMO, and BAMO. The strain energy (SE) for the oxetane derivatives were calculated using homodesmotic reactions, while intramolecular group interactions were predicted through the disproportionation energies. The concept of chemical hardness is used to analyze the susceptibility of designed compounds to reactivity and chemical transformations. The heats of formation, density, and predicted performance imply that the designed molecules are expected to be candidates for polymer synthesis and potential molecules for energetic binders.

  6. Solubilities of sub- and supercritical carbon dioxide in polyester resins

    NARCIS (Netherlands)

    Nalawade, SP; Picchioni, F; Janssen, LPBM; Patil, VE; Keurentjes, JTF; Staudt, R; Nalawade, Sameer P.; Patil, Vishal E.; Keurentjes, Jos T.F.

    In supercritical carbon dioxide (CO2) assisted polymer processes the solubility of CO2 in a polymer plays a vital role. The higher the amount of CO2 dissolved in a polymer the higher is the viscosity reduction of the polymer. Solubilities Of CO2 in polyester resins based on propoxylated bisphenol

  7. Investigation on Water Jet Treated Polyester/cotton Blended Cambric

    Institute of Scientific and Technical Information of China (English)

    黄故

    2004-01-01

    Analytical examination was made to ascertain the effect of the high pressure water flow on the fabric properties.Polyester/cotton blended cambric was spurted by high pressure water flow. Fabric properties such as handle,thickness, tensile strength , stiffness and air permeability after the water treatment were investigated.

  8. Mechanical and Morphological Properties of Nano Filler Polyester Composites

    Directory of Open Access Journals (Sweden)

    Bonnia Noor Najmi

    2016-01-01

    Full Text Available This research is focusing on mechanical and morphological properties of unsaturated polyester (UP reinforced with two different types of filler which is nano size clay Cloisite 30B (C30B and Carbon Black (CB. Samples were fabricated via hand lay-up and open molding technique. Percentages of Cloisite 30B & Carbon Black (CB used vary from 0, 2, 4, 6, 8 and 10 wt%. The mechanical properties were evaluated by impact, flexural and hardness testing. Result shows that the mechanical strength of C30B was better compare to CB filled composite. The combination of UP with C30B helps to improve the properties due to the high surface area of nanosize filler in the matrix. The result shows that increasing of filler content had increased mechanical properties of composites. Optimum percentage represent good mechanical properties are 4% for both fillers. SEM images showed that rough surface image indicate to agglomeration of filler in the matrix for CB sample and smooth surface image on C30B sample indicate to homogenous blending between filler and matrix polyester. SEM images proved that mechanical properties result indicate that C30B polyester composite is a good reinforcement compare to CB polyester composite.

  9. Propagation of polarized light through azobenzene polyester films

    DEFF Research Database (Denmark)

    Nedelchev, L; Matharu, A; Nikolova, Ludmila

    2002-01-01

    When elliptically polarized light of appropriate wavelength Corresponding to trans-cis-trans isomerisation process is incident on thin films of azobenzene polyesters, a helical structure is induced. We investigate the propagation of the exciting light beam (self-induced) as well as a probe light...

  10. Adsorption of proteins from plasma at polyester non-wovens

    NARCIS (Netherlands)

    Klomp, A.J.A.; Engbers, G.H.M.; Mol, J.; Terlingen, J.G.A.; Feijen, J.

    1999-01-01

    Polyester non-wovens in filters for the removal of leukocytes from platelet concentrates (PCs) must be platelet compatible. In PC filtration, the adsorption of proteins at the plasma–non-woven interface can be of great importance with respect to the yield of platelets. Unmodified and radio frequency

  11. Blends of Amphiphilic, Hyperbranched Polyesters and Different Polyolefins

    NARCIS (Netherlands)

    Schmaljohann, D.; Pötschke, P.; Hässler, R.; Voit, B.I.; Froehling, P.E.; Mostert, B.; Loontjens, J.A.

    1999-01-01

    A hyperbranched polyester based on 3,5-dihydroxybenzoic acid was completely modified with dodecanoyl chloride to result in an amphiphilic, globular polymer, which has a polar core and a nonpolar outer sphere with the ability both to incorporate an organic dye and to interact with a nonpolar matrix.

  12. Advanced microgel-functionalized polyester textiles adaptive to ambient conditions

    NARCIS (Netherlands)

    Glampedaki, Pelagia

    2011-01-01

    A new approach toward textile-based multi-functional and stimuli-responsive materials is proposed. Polyelectrolyte microgel technology is combined with conventional functionalization methods of photo- and thermo-crosslinking to activate the surface of polyester textiles, making them interactive with

  13. Photoinduced Circular Anisotropy in Side-Chain Azobenzene Polyesters

    DEFF Research Database (Denmark)

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

    1997-01-01

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

  14. Solubilities of sub- and supercritical carbon dioxide in polyester resins

    NARCIS (Netherlands)

    Nalawade, SP; Picchioni, F; Janssen, LPBM; Patil, VE; Keurentjes, JTF; Staudt, R; Nalawade, Sameer P.; Patil, Vishal E.; Keurentjes, Jos T.F.

    2006-01-01

    In supercritical carbon dioxide (CO2) assisted polymer processes the solubility of CO2 in a polymer plays a vital role. The higher the amount of CO2 dissolved in a polymer the higher is the viscosity reduction of the polymer. Solubilities Of CO2 in polyester resins based on propoxylated bisphenol (P

  15. Microcellular processing of polylactide-hyperbranched polyester-nanoclay composites

    Science.gov (United States)

    Srikanth Pilla; Adam Kramschuster; Jungjoo Lee; Craig Clemons; Shaoqin Gong; Lih-Sheng Turng

    2010-01-01

    The effects of addition of hyperbranched polyesters (HBPs) and nanoclay on the material properties of both solid and microcellular polylactide (PLA) produced via a conventional and microcellular injection-molding process, respectively, were investigated. The effects of two different types of HBPs (i.e., Boltorn H2004® and Boltorn H20®) at the same...

  16. MERSILENE (POLYESTER), A NEW SUTURE FOR PENETRATING KERATOPLASTY

    NARCIS (Netherlands)

    RAMSELAAR, JAM; BEEKHUIS, WH; RIJNEVELD, WJ; VANANDEL, MV; DIJK, F; JONGEBLOED, WL

    1992-01-01

    Mersilene (polyester monofilament) seems to be suitable for penetrating keratoplasty because it is strong, shows no degradation by ultraviolet light, is insoluble, so that it can be left in situ, and offers the possibility of regulating postoperative astigmatism by suture adjustment. In 12 patients

  17. Highly Branched Bio-Based Unsaturated Polyesters by Enzymatic Polymerization

    Directory of Open Access Journals (Sweden)

    Hiep Dinh Nguyen

    2016-10-01

    Full Text Available A one-pot, enzyme-catalyzed bulk polymerization method for direct production of highly branched polyesters has been developed as an alternative to currently used industrial procedures. Bio-based feed components in the form of glycerol, pentaerythritol, azelaic acid, and tall oil fatty acid (TOFA were polymerized using an immobilized Candida antarctica lipase B (CALB and the potential for an enzymatic synthesis of alkyds was investigated. The developed method enables the use of both glycerol and also pentaerythritol (for the first time as the alcohol source and was found to be very robust. This allows simple variations in the molar mass and structure of the polyester without premature gelation, thus enabling easy tailoring of the branched polyester structure. The postpolymerization crosslinking of the polyesters illustrates their potential as binders in alkyds. The formed films had good UV stability, very high water contact angles of up to 141° and a glass transition temperature that could be controlled through the feed composition.

  18. The practice of using Phenol inhibitors in obtaining monomers

    Energy Technology Data Exchange (ETDEWEB)

    Kurbatov, V.A.; Kirpichnikov, P.A.; Likumovich, A.G.

    1983-01-01

    Phenol antioxidants are promising stabilizers for the industrial production of monomers. Their potential may be considerably improved by searching for optimum compositions and conditions of application.

  19. Can the hydrophilicity of functional monomers affect chemical interaction?

    Science.gov (United States)

    Feitosa, V P; Ogliari, F A; Van Meerbeek, B; Watson, T F; Yoshihara, K; Ogliari, A O; Sinhoreti, M A; Correr, A B; Cama, G; Sauro, S

    2014-02-01

    The number of carbon atoms and/or ester/polyether groups in spacer chains may influence the interaction of functional monomers with calcium and dentin. The present study assessed the chemical interaction and bond strength of 5 standard-synthesized phosphoric-acid ester functional monomers with different spacer chain characteristics, by atomic absorption spectroscopy (AAS), ATR-FTIR, thin-film x-ray diffraction (TF-XRD), scanning electron microscopy (SEM), and microtensile bond strength (μTBS). The tested functional monomers were 2-MEP (two-carbon spacer chain), 10-MDP (10-carbon), 12-MDDP (12-carbon), MTEP (more hydrophilic polyether spacer chain), and CAP-P (intermediate hydrophilicity ester spacer). The intensity of monomer-calcium salt formation measured by AAS differed in the order of 12-MDDP=10-MDP>CAP-P>MTEP>2-MEP. FTIR and SEM analyses of monomer-treated dentin surfaces showed resistance to rinsing for all monomer-dentin bonds, except with 2-MEP. TF-XRD confirmed the weaker interaction of 2-MEP. Highest µTBS was observed for 12-MDDP and 10-MDP. A shorter spacer chain (2-MEP) of phosphate functional monomers induced formation of unstable monomer-calcium salts, and lower chemical interaction and dentin bond strength. The presence of ester or ether groups within longer spacer carbon chains (CAP-P and MTEP) may affect the hydrophilicity, μTBS, and also the formation of monomer-calcium salts.

  20. Interference of functional monomers with polymerization efficiency of adhesives.

    Science.gov (United States)

    Hanabusa, Masao; Yoshihara, Kumiko; Yoshida, Yasuhiro; Okihara, Takumi; Yamamoto, Takatsugu; Momoi, Yasuko; Van Meerbeek, Bart

    2016-04-01

    The degree of conversion (DC) of camphorquinone/amine-based adhesives is affected by acidic functional monomers as a result of inactivation of the amine co-initiator through an acid-base reaction. During bonding, functional monomers of self-etch adhesives chemically interact with hydroxyapatite (HAp). Here, we tested in how far the latter interaction of functional monomers with HAp counteracts the expected reduction in DC of camphorquinone/amine-based adhesives. The DC of three experimental adhesive formulations, containing either of the two functional monomers [10-methacryloyloxydecyl dihydrogen phosphate (10-MDP) or 4-methacryloxyethyl trimellitic acid anhydride (4-META)] or no functional monomer (no-FM; control), was measured with and without HAp powder added to the adhesive formulations. Both the variables 'functional monomer' and 'HAp' were found to be significant, with the functional monomer reducing the DC and HAp counteracting this effect. It is concluded that the functional monomers 10-MDP and 4-META interfere with the polymerization efficiency of adhesives. This interference is less prominent in the presence of HAp, which would clinically correspond to when these two functional monomers of the adhesive simultaneously interact with HAp in tooth tissue.

  1. Dyeing of Polyester with Disperse Dyes: Part 2. Synthesis and Dyeing Characteristics of Some Azo Disperse Dyes for Polyester Fabrics

    Directory of Open Access Journals (Sweden)

    Alya M. Al-Etaibi

    2016-06-01

    Full Text Available The goal of this study was to utilize carrier for accelerating the rate of dyeing not only to enhance dyeing of polyester fabrics dyed with disperse dyes 3a,b, but also to save energy. Both the color strength expressed as dye uptake and the fastness properties of the dyed fabrics were evaluated.

  2. A review of the developments of multi-purpose primers and adhesives comprising novel dithiooctanoate monomers and phosphonic acid monomers.

    Science.gov (United States)

    Ikemura, Kunio; Endo, Takeshi; Kadoma, Yoshinori

    2012-02-03

    This paper reviews the developments of dithiooctanoate monomers and acidic adhesive monomers, and their roles in multi-purpose primers and adhesives in promoting adhesion to multiple substrate materials. Novel dithiooctanoate monomers exhibited excellent bonding to precious metals and alloys when compared against conventional sulfur-containing monomers. Newly developed phosphonic acid monomers, endowed with a water-soluble nature, enabled sufficient demineralization of dental hard tissues and thus improved bonding to both ground enamel and dentin. The optimal combination for bonding to dental hard tissues and precious and non-precious metals and alloys was 5.0 wt% 10-methacryloyloxydecyl 6,8-dithiooctanoate (10-MDDT) and 1.0 wt% 6-methacryloyloxyhexyl phosphonoacetate (6-MHPA). For bonding to dental porcelain, alumina, zirconia, and gold (Au) alloy, a ternary combination of silane coupling agent, acidic adhesive monomers, and dithiooctanoate monomers seemed promising. The latest development was a single-bottle, multi-purpose, self-etching adhesive which contained only acidic adhesive monomers and dithiooctanoate monomers but which produced strong adhesion to ground enamel and dentin, sandblasted zirconia, and Au alloy.

  3. Macromolecular Engineering: New Routes Towards the Synthesis of Well-??Defined Polyethers/Polyesters Co/Terpolymers with Different Architectures

    KAUST Repository

    Alamri, Haleema

    2016-05-18

    styrene oxide (SO) monomer has been less investigated than other well-known epoxide monomers. The new one?pot synthesis of polyether?b?polyester block copolymers allowed a high degree of control with respect to the molecular weight and molecular weight distribution. It also eliminates the need for a multi-step process in which the first block must be isolated and purified prior to its subsequent use as a macroinitiator for the second block. It is also worth noting that this approach is based primarily on the use of organocatalyst because this class of block copolymers has greater potential in biomedical and pharmaceutical applications and because organocatalysts are believed to be less toxic than their metallic counterparts. The fourth part of the thesis describes the extension of the scope of the newly developed catalyst?switching approach in the synthesis of different macromolecular architectures, with a special focus on styrene oxide as a monomer, which had not previously been explored either as a linear copolymer with other monomers (except with EO) or with a macromolecular architecture such as block star or mikto arm star. The results detailed in Chapter 4 demonstrate the validity of extending the newly developed strategy to the synthesis of a variety of polymers with different macromolecular architectures. Since organic catalysts (phoshazene bases) have been utilized in this work for the synthesis of polyethers and polyesters with the aim of alleviating the toxic properties associated with metal-based catalysts, it was necessary to investigate the toxicity of this class of organocatalyst since, until now, no evidence has appeared of any attempt to address this issue. The objective of the work presented in the fifth part of this thesis was therefore to assess whether this class of organocatalysts are safe with respect to human health and whether their structure and concentration are dependent on an evaluation of the level of cytotoxicity or on other parameters. Both

  4. 水性聚酯对氧化淀粉膜力学性能的影响%Effect of Water-soluble Polyester on Mechanical Property of Oxidized Starch Film

    Institute of Scientific and Technical Information of China (English)

    陈试伟; 朱谱新; 胡晓

    2012-01-01

    Effect of water-soluble polyester on structure and mechanical property of starch film were studied. Oxidized starch/water-soluble polyester blend film with different polyester contents was prepared by adopting casting method. Effect of water-soluble polyester on starch film structure was discussed through ATR-FTIR method and X-ray diffraction method, and mechanical property of starch film was tested. The result shows that formation of hydrogen bonds in oxidized corn starch can be enhanced by water-soluble polyester, and amorphous region and chain entanglement of oxidized corn starch molecules were increased, while there was no hydrogen bond formed between oxidized corn starch and water-soluble polyester molecules. Crystallinity of the starch films is decreased with the increase of the water-soluble polyester content, while the crystallization shape is not affected. Initial modulus of the starch films is decreased by water-soluble polyester,while the breaking elongation of the film is improved. It is pointed out that water-soluble polyester is helpful to modify brittle defect of the starch film.%研究水性聚酯对淀粉浆膜结构和力学性能的影响.采用浇注成膜法制备了不同水性聚酯含量的氧化淀粉/水溶性聚酯混合膜.通过衰减全反射红外法、X-射线衍射法探讨了水性聚酯对淀粉浆膜结构的影响,并测定了浆膜的机械性能.结果表明,水性聚酯促进了氧化玉米淀粉分子间氢键的形成,增加了玉米氧化淀粉分子的链缠结和无定形区,而氧化玉米淀粉与水性聚酯之间并没有氢键形成;水性聚酯含量增加会使浆膜结晶度逐渐下降,但并未对其结晶形态造成影响;水性聚酯降低了浆膜的初始模量,提高了浆膜的断裂伸长.指出:水性聚酯的加入有助于改善淀粉浆膜的脆硬性.

  5. Plasma-Enhanced Copolymerization of Amino Acid and Synthetic Monomers

    Science.gov (United States)

    2011-12-16

    end cap containing a second inlet for the liquid monomer delivery (Scheme 1). The solid L-tyrosine monomer was placed in a resistively heated tantalum ...microroughness, which is indicative of uniform cross-linking and wetting of the deposits of all components. These films are free of pinhole defects as well

  6. The influence of molecular structure on the hydrolysability of unsaturated polyester resins; Influence de la structure moleculaire sur l`hydrolysabilite des resines polyester insature

    Energy Technology Data Exchange (ETDEWEB)

    Spiteri, P.; Denis, V.; Fontanille, M.; Villenave, J.J.

    1993-04-01

    The influence of the structure of polyester resins on their water absorption processes has been evidenced. Correlations have been established between the kinetics of the absorption of water and the hydrolytic degradation of the materials. They allow to propose a method for predicting the life time of unsaturated polyester materials. (authors). 1 tab., 5 figs., 5 refs.

  7. Oligonucleotides with 1,4-dioxane-based nucleotide monomers

    DEFF Research Database (Denmark)

    Madsen, Andreas S; Wengel, Jesper

    2012-01-01

    An epimeric mixture of H-phosphonates 5R and 5S has been synthesized in three steps from known secouridine 1. Separation of the epimers has been accomplished by RP-HPLC, allowing full characterization and incorporation of monomers X and Y into 9-mer oligonucleotides using H-phosphonates building...... blocks 5R and 5S, respectively. A single incorporation of either monomer X or monomer Y in the central position of a DNA 9-mer results in decreased thermal affinity toward both DNA and RNA complements (ΔT(m) = -3.5 °C/-3.5 °C for monomer X and ΔT(m) = -11.0 °C/-6.5 °C for monomer Y). CD measurements do...

  8. Monomer-dimer tatami tilings of square regions

    CERN Document Server

    Erickson, Alejandro

    2011-01-01

    We prove that the number of monomer-dimer tilings of an $n\\times n$ square grid, with $mmonomers in which no four tiles meet at any point is $m2^m+(m+1)2^{m+1}$, when $m$ and $n$ have the same parity. In addition, we present a new proof of the result that there are $n2^{n-1}$ such tilings with $n$ monomers, which divides the tilings into $n$ classes of size $2^{n-1}$. The sum of these tilings over all monomer counts has the closed form $2^{n-1}(3n-4)+2$ and, curiously, this is equal to the sum of the squares of all parts in all compositions of $n$. We also describe two algorithms and a Gray code ordering for generating the $n2^{n-1}$ tilings with $n$ monomers, which are both based on our new proof.

  9. Evaluation Study of Glass Fiber Reinforced Polyester and Kevlar Reinforced Polyester by Taguchi Method

    Directory of Open Access Journals (Sweden)

    Osama Sultan M.

    2012-01-01

    Full Text Available In the present investigation two different types of fiber reinforced polymer composites were prepared by hand lay-up method using three different parameters (curing temperature, pressing load and fiber volume fraction. These composites were prepared from the polyester resin as the matrix material reinforced with glass fibers as first group of samples and mat Kevlar fibers as the second group, both with different volume fractions (4%, 8%, and 12% of fibers. They were then tested by tensile strength and impact strength. The main objective in this study is to use Taguchi method for predicting the better parameters that give the better tensile and impact strength to the composites, and then preparing composites at these parameters and comparing them with the randomly used once. The experimental and analytical results showed that the Taguchi method was successful in optimizing the parameters that give the highest properties and it can find the most influential parameter regardless of the material used. Also it showed that the volume fraction was the most influential parameter on the tensile and impact strength. The difference between these composites was in the properties values and that the Kevlar composites have higher tensile and impact strength.

  10. STUDY ON SYNTHESIS AND RELAXIVITY OF PARAMAGNETIC POLYESTER METAL COMPLEXES FOR MRI

    Institute of Scientific and Technical Information of China (English)

    Ouyangming; ZhuoRenxi; 等

    1995-01-01

    Fifteen new polyester ligands were prepared by copolymerization of EDTA (ethylenediaminetertraacetic acid)dianhydride or DTPA (diethylenetriamine pentaacetic acid) dianhydride and dihydric alcohol or dihydric phenol.Their paramagnetic metal complexes were also synthesized.All polyester ligands and metal complexes were characterized by 1HNMR,IR spectra and elemental analyses.Preliminary study showed that the polyester metal complexes had higher relaxation effectiveness as compared to corresponding small molecular metal complexes.

  11. Study on the improvement of hydrophilic character on polyvinylalcohol treated polyester fabric

    OpenAIRE

    S. Pitchai; J. Jeyakodi Moses; Natarajan Swarna

    2014-01-01

    Polyester fabric was treated with polyvinyl alcohol in alkaline medium. The moisture regain, water retention and wettability of the PVA treated polyester fabric were tested. The PVA treated PET fabric was dyed with disperse dye. The presence of PVA in the treated PET fabric was assessed by spot test. The treated fabric was also characterized by scanning electron microscope, FTIR and differential scanning calorimetry. The PVA treated polyester fabric showed improved hydrophilic character over ...

  12. Transcaval access for TAVR across a polyester aortic graft.

    Science.gov (United States)

    Lederman, Robert J; O'Neill, William W; Greenbaum, Adam B

    2015-06-01

    Transcaval access to the aorta allows transcatheter aortic valve replacement in patients without other good access options. The resulting aorto-caval fistula is closed with a nitinol cardiac occluder device. There is no experience traversing a synthetic aortic graft to perform transcaval access and closure. We describe a patient who underwent successful traversal of a polyester aortic graft using radiofrequency energy applied from the tip of a guidewire, to allow retrograde transcatheter aortic valve replacement from a femoral vein, along with details of our technique. The patient did well and was discharged home after 3 days. There was residual aorto-caval fistulous flow immediately after implantation of a polyester-seeded nitinol muscular ventricular septal defect occluder device, but this fistula spontaneously occluded within one month.

  13. Drilling analysis of coir–fibre-reinforced polyester composites

    Indian Academy of Sciences (India)

    S Jayabal; U Natarajan

    2011-12-01

    An investigation has been carried out to make use of coir, a natural fibre abundantly available in India. Coir–polyester composites were prepared and their mechanical and machinability characteristics were studied. The short coir–fibre-reinforced composites exhibited the tensile, flexural and impact strength of 16.1709 MPa, 29.2611 MPa and 46.1740 J/m, respectively. The regression equations were developed and optimized for studying drilling characteristics of coir–polyester composites using the Taguchi approach. A drill bit diameter of 6 mm, spindle speed of 600 rpm and feed rate of 0.3 mm/rev gave the minimum value of thrust force, torque and tool wear in drilling analysis.

  14. Recent developments in lipase-catalyzed synthesis of polyesters.

    Science.gov (United States)

    Kobayashi, Shiro

    2009-02-18

    Polyester synthesis by lipase catalyst involves two major polymerization modes: i) ring-opening polymerization of lactones, and, ii) polycondensation. Ring-opening polymerization includes the finding of lipase catalyst; scope of reactions; polymerization mechanism; ring-opening polymerization reactivity of lactones; enantio-, chemo- and regio-selective polymerizations; and, chemoenzymatic polymerizations. Polycondensation includes polymerizations involving condensation reactions between carboxylic acid and alcohol functional groups to form an ester bond. In most cases, a carboxylic acid group is activated as an ester form, such as a vinyl ester. Many recently developed polymerizations demonstrate lipase catalysis specific to enzymatic polymerization and appear very useful. Also, since lipase-catalyzed polyester synthesis provides a good opportunity for conducting "green polymer chemistry", the importance of this is described.

  15. Rear Bumper Laminated In Jute Fiber With Polyester Resin.

    Directory of Open Access Journals (Sweden)

    Braga, R. A

    2014-09-01

    Full Text Available Today, a growing interest exists in the use of natural of fibers (sisal, coconut, banana, and jute, as reinforcement in composites. The aim of the present study is shows the use of jute fiber agglutinated with polyester resin in the automobile industry in the production of a rear bumper of hatch vehicle. A simplified mathematical model was used for evaluation of the flaw on trunk center cover submitted to dynamic loads. The traverse section of the referred bumper is simplified by a channel formation. This study shows that a rear bumper made using jute fiber agglutinated with polyester resin will be possible. The molded part obtained good visual characteristics, good geometric construction and surface without bubbles and imperfections in the fiber and resin composite. The mathematical model to failure criterion showed that the rear bumper in jute fiber will not resist to an impact equivalent at 4.0 km/h.

  16. Neutron shielding performance of water-extended polyester

    Energy Technology Data Exchange (ETDEWEB)

    Vega Carrillo, H.R.; Manzanares-Acuna, E.; Hernandez-Davila, V.M. [Zacatecas Univ. Autonoma, Nuclear Studies (Mexico); Vega Carrillo, H.R.; Hernandez-Davila, V.M. [Zacatecas Univ. Autonoma, Electric Engineering Academic Units (Mexico); Gallego, E.; Lorente, A. [Madrid Univ. Politecnica, cNuclear Engineering Department (Mexico)

    2006-07-01

    A Monte Carlo study to determine the shielding features to neutrons of water-extended polyester (WEP) was carried out. Materials with low atomic number are predominantly used for neutron shielding because these materials effectively attenuate neutrons, mainly through elastic and inelastic collisions. In addition to neutron attenuation properties, other desirable properties for neutron shielding materials include mechanical strength, stability, low cost, and ease of handling. During the selection of materials to design a neutron shield, prompt gamma production as well as radionuclide induced by neutron activation must be considered. In this investigation the Monte Carlo method (MCNP code) was used to evaluate the performance of a water-extended polyester shield designed for the transportation, storage, and use of a {sup 252}Cf isotopic neutron source, for comparison the calculations were extended to water shielding, the bare source in vacuum and in air. (authors)

  17. Synthesis and Application of Easy Hydrolysis Degradable Polyester

    Institute of Scientific and Technical Information of China (English)

    张大省; 李燕立; 陈英; 付中玉; 王锐; 李梅

    2001-01-01

    An easy hydrolysis degradable polyester (EHDP) is synthesized; the fiber produced from which can be hydrolyzed by dilute basic solution easily. The properties of these kind polyesters are measured. The results show that this kind polymer is suitable to be spun into filament The EHDP can be spun into staple fiber and manufactured into non-woven fabric. This fabric is used as disposable clothes. In composite spinning, the PET (polyethylen glycol terephthalate) or PA (polyamide) is used as continuous phase, and EHDP used as dispersed phase. Then the fabric of this kind fiber is treated by basic solution; the ultra-fine fiber fabric is obtained.The fineness of the fiber is about 0.045 dtex. In blend spinning, EHDP is mixed with polypropylene (PP) to produce hollow fiber with micro-holes in radical direction. This fiber is a usable material in filter especially in medical use.

  18. Tensile strength of woven yarn kenaf fiber reinforced polyester composites

    Directory of Open Access Journals (Sweden)

    A.E. Ismail

    2015-12-01

    Full Text Available This paper presents the tensile strength of woven kenaf fiber reinforced polyester composites. The as-received yarn kenaf fiber is weaved and then aligned into specific fiber orientations before it is hardened with polyester resin. The composite plates are shaped according to the standard geometry and uni-axially loaded in order to investigate the tensile responses. Two important parameters are studied such as fiber orientations and number of layers. According to the results, it is shown that fiber orientations greatly affected the ultimate tensile strength but it is not for modulus of elasticity for both types of layers. It is estimated that the reductions of both ultimate tensile strength and Young’s modulus are in the range of 27.7-30.9% and 2.4-3.7% respectively, if the inclined fibers are used with respect to the principal axis.

  19. Fabrication of Biodegradable Polyester Nanocomposites by Electrospinning for Tissue Engineering

    Directory of Open Access Journals (Sweden)

    Zhi-Cai Xing

    2011-01-01

    Full Text Available Recently, nanocomposites have emerged as an efficient strategy to upgrade the structural and functional properties of synthetic polymers. Polyesters have attracted wide attention because of their biodegradability and biocompatibility. A logic consequence has been the introduction of natural extracellular matrix (ECM molecules, organic or inorganic nanostructures to biodegradable polymers to produce nanocomposites with enhanced properties. Consequently, the improvement of the interfacial adhesion between biodegradable polymers and natural ECM molecules or nanostructures has become the key technique in the fabrication of nanocomposites. Electrospinning has been employed extensively in the design and development of tissue engineering scaffolds to generate nanofibrous substrates of synthetic biodegradable polymers and to simulate the cellular microenvironment. In this paper, several types of biodegradable polyester nanocomposites were prepared by electrospinning, with the aim of being used as tissue engineering scaffolds. The combination of biodegradable nanofibrous polymers and natural ECM molecules or nanostructures opens new paradigms for tissue engineering applications.

  20. HEMA inhibits interfacial nano-layering of the functional monomer MDP.

    Science.gov (United States)

    Yoshida, Y; Yoshihara, K; Hayakawa, S; Nagaoka, N; Okihara, T; Matsumoto, T; Minagi, S; Osaka, A; Van Landuyt, K; Van Meerbeek, B

    2012-11-01

    Previous research showed that the functional monomer 10-methacryloxydecyl dihydrogen phosphate (MDP) ionically bonds to hydroxyapatite (HAp) and forms a nano-layered structure at the interface with HAp-based substrates. Such hydrophobic nano-layering is considered to contribute to the long-term durability of the bond to tooth tissue. However, dental adhesives are complex mixtures usually containing different monomers. This study investigated the effect of the monomer 2-hydroxyethylmethacrylate (HEMA) on the chemical interaction of MDP with HAp by x-ray diffraction (XRD), nuclear magnetic resonance (NMR), and quartz crystal microbalance (QCM). We examined the chemical interaction of 5 experimental MDP solutions with increasing concentrations of HEMA. XRD revealed that addition of HEMA inhibits nano-layering at the interface, while NMR confirmed that MDP remained adsorbed onto the HAp surface. QCM confirmed this adsorption of MDP to HAp, as well as revealed that the demineralization rate of HAp by MDP was reduced by HEMA. It was concluded that even though the adsorption of MDP to HAp was not hindered, addition of HEMA inhibited interfacial nano-layering. Potential consequences with regard to bond durability necessitate further research.

  1. Fiberglass wastes/polyester resin composites: mechanical properties and water sorption

    Directory of Open Access Journals (Sweden)

    Edcleide M. Araújo

    2006-12-01

    Full Text Available The mechanical properties of polyester/fiberglass composites were studied. The aim of this work was to evaluate the possibility of reusing the wastes taken from spray-up processing of Paraíba state Industries as reinforcement in polyester matrix composites. Composites with 20, 30, 40, 50 and 60 wt. (% of recycled fiberglass were prepared by compression molding and compared with polyester/ virgin glass fiber composites. The mechanical properties and water sorption behavior were evaluated. The results showed that fiberglass wastes are promising to be reused in polyester resin composites. The impact strength was excellent. It can be concluded that the reusing of the fiberglass wastes is viable.

  2. Healthy Functions and Mechanisms of Bamboo-Charcoal Modified Polyesters

    Institute of Scientific and Technical Information of China (English)

    WANG Qi; HE Shu-cai

    2007-01-01

    In this paper, healthy fuactions and mechanismof bamboo-charcoal modified polyesters arc studied. Theresults show that there are five healthy functionsincorporated effectively in bamboo-charcoal modifiedpolyesters, such as good far-lnfrared radiation, good UVprotection, certain negative ion emission, certain anti-bacteria and good absorption functions. The metal elementsand carburets are mainly responsible for far-infrared,negative ion emission functions. UV prevention functionresults mainly from the carbon elements. The absorbabilityand bacteriostasis functions lie in the porous structures.

  3. The interlaminar strength of the glass fiber polyester composite

    Directory of Open Access Journals (Sweden)

    S. Putić

    2009-01-01

    Full Text Available The paper outlines the method and the results of the experimental investigation of interlaminar strength of glass fibre reinforced polyester composites, with the aim of determining the influence that the structure, a reinforcement type and a sort of resin exert upon the interlaminar strength. The tested specimens were fabricated under different formation conditions, namely in eight composition patterns and with three sorts of resin used for polymerization.

  4. SYNTHESIS AND CHARACTERIZATION OF AN ORDERED LADDER POLYESTER

    Institute of Scientific and Technical Information of China (English)

    Ping-ping Zhang; Tao-yi Zhang; Chuan-feng Zhu; Yu-xia Diao; You-zhi Wan; Ping Xie; Rong-ben Zhang

    2006-01-01

    An ordered ladder polyester (LPE) was first synthesized through the ladder superstructure (LS) constructed by concerted interactions of hydroxyl- and aramide-based H-bonding and p-terphenyl (TP)-based π-stacking by dehydrochlorination condensation using phosgene (COCl2) as coupling agent. LPE was characterized by GPC, FTIR, NMR,XRD, DSC and AFM. Among them, a distinct image of regularly linear alignment corresponding to the ladder main chain of LPE was first revealed by high-resolution AFM.

  5. Study on the preirradiation polymerization of vinyl monomers

    Science.gov (United States)

    Yu-Ming, Liu; Yue-Qi, Yang; Zue-Teh, Ma

    This paper presents mainly the polymerization, copolymerization and crosslinking of monomers off-source induced by peroxides which are formed by high energy irradiation of vinyl monomers such as styrene (St), acrylonitrile (AN), methylmethacrylate (MMA), vinyl acetate (VAc) and 2-hydroxyethyl methacrylate (HEMA). The peroxides produced by irradiation of the above-mentioned monomers can not only induce the monomers themselves, but also another non-irradiated monomer to carry out copolymerization efficiently. The activation energy of peroxide formation, the apparent activation energy of polymerization and the activation energy of peroxide initiation by irradiation of vinyl monomers are: Ef(MMA) = 11, Ef(St) = 9.6, Ef(AN) = 8.5, EMMA = EVA = 11.4, Ei(MMA) = Ei(VA) = 13 kcal/mol. The rate of decomposition of monomer peroxides is smoother than that of BPO during the polymerization and so a smooth kinetic progress is obtained. The initiating ability of forming peroxides by irradiation of the vinyl monomers depends mainly on the chemical structure of the monomers. For instance, the main structure of peroxides formed during preirradiation MMA are: alternating peroxy-copolymer ? and random peroxy-copolymer ? Owing to the peroxy-bond which is unstable and in which homolytic breakage easily occurs to yield a pair of radicals, RO . is formed within the above-mentioned structural compounds, so that they possess stronger initiating reactivity. It is quite evident that the initiating reactivity of AN peroxide will be greatly reduced because of the conjugate double bond. In other words, the initiating ability of AN peroxide is lower than MMA peroxide and St peroxide.

  6. A multi-scale method for modeling degradation of bioresorbable polyesters.

    Science.gov (United States)

    Zhang, Taohong; Zhou, Shaonan; Gao, Xiaohao; Yang, Zhiyong; Sun, Leran; Zhang, Dezheng

    2017-03-01

    A multi-scale model using the cellular automata (CA) and kinetic Monte Carlo (KMC) methods is presented to simulate the degradation process of bioresorbable polyesters such as polylactide (PLA), polyglycolide (PGA) and their copolymers. The model considers the underlying chemical and physical events such as polymer chain scission, oligomer production, crystallization induced by polymer chain scissions, oligomer diffusion and microstructure evolution due to erosion of the small chains. A macroscopic device is discretized into an array of mesoscopic cells. Each cellular lattice is assumed to be made of one polymer chain, which undergoes hydrolysis reaction. The polymer chain scission is modeled using a kinetic Monte Carlo method. Oligomer production, chain crystallization and formation of cavities due to polymer collapse are also modeled on the cellular lattice. Oligomer diffusion is modeled by using Fick's laws at the macroscopic scale. The diffusion coefficient is taken as dependent on the porosity caused by the formation of the cavities. The interactions among the microscopic hydrolysis reaction, mesoscopic formation of cavities and macroscopic diffusion are taken into account. The proposed method forms Multi Scale Cellular Monte Carlo Automata (MS-CMCA). The three-scale approach consists of continuous method and discrete method to deal with certainty problem with underlying stochastic phenomenon. Demonstration examples are provided which show that the model can fit with experimental data in the literature very well.

  7. Structure and morphology of thin films of linear aliphatic polyesters prepared by spin-coating.

    Science.gov (United States)

    Hernández, J J; Rueda, D R; García-Gutiérrez, M C; Nogales, A; Ezquerra, T A; Soccio, M; Lotti, N; Munari, A

    2010-07-06

    Thin films, with thicknesses from 10 to 400 nm of linear aliphatic polyesters (X, Y), based on propylenediol (X = 3) and on dicarboxylic acid of different chain length (Y = 2, 3, and 4 CH(2) units) were prepared by spin coating of CHCl(3) polymer solutions with different polymer concentrations. Morphology and structure of the spin coated thin films were investigated by atomic force microscopy (AFM) and by grazing incidence X-ray scattering techniques at small, (GISAXS) and wide angles (GIWAXS). AFM revealed a strong dewetting for all three polymers for coatings thinner than 100 nm. The polymer films are clearly semicrystalline for thicknesses higher than 50 nm. GIWAXS of the thicker films revealed their oriented crystalline nature. An edge-on-lamellae morphology is clearly shown by the AFM-phase images even for relatively thin films. SAXS with the beam parallel to the sample plane also support the presence of lamellae perpendicular to the substrate. The use of a mu-beam helped to interpret the GIWAXS patterns and allowed to obtain oriented WAXS patterns from melt solidified filaments. Thus, a crystal chain packing is proposed for the three polymers and consequently the indexing of the observed reflections. Accordingly, the polymer chains lie parallel to the substrate being the bc plane of the monoclinic crystal unit cell parallel to the substrate.

  8. Highly Efficient Synthesis of Allopurinol Locked Nucleic Acid Monomer by C6 Deamination of 8-Aza-7-bromo-7-deazaadenine Locked Nucleic Acid Monomer

    DEFF Research Database (Denmark)

    Kosbar, Tamer Reda El-Saeed; Sofan, M.; Abou-Zeid, L.;

    2013-01-01

    An allopurinol locked nucleic acid (LNA) monomer was prepared by a novel strategy through C6 deamination of the corresponding 8-aza-7-bromo-7-deazaadenine LNA monomer with aqueous sodium hydroxide. An 8-aza-7-deazaadenine LNA monomer was also synthesized by a modification of the new synthetic pat...... the required LNA monomers. © Georg Thieme Verlag....

  9. Thermally-responsive poly(ester urethane)s

    Science.gov (United States)

    Pierce, Benjamin Franklin

    Thermally-responsive materials are quite useful in the biomedical field, but their full potential has yet to be realized. For example, polyurethanes are capable of exhibiting shape-memory properties, or the ability to change shape upon the application of a stimulus, but only a few practical thermally responsive polyurethanes have been reported due to the lack of novel starting materials and optimized systems. This work describes the synthesis of several degradable polymers and the characterization of their thermally responsive behavior. First, several amorphous polyester prepolymers are synthesized and incorporated in thermoplastic poly(ester urethane)s, which are highly elastic but display impractical thermal properties. Their potential as degradable implants is investigated, as well as their bulk and surface properties. These systems are then optimized and tailored for more practical purposes, resulting in the synthesis of thermoset elastomers based on poly(1,4-cyclohexanedimethanol 1,4-cyclohexanedicarboxylate) (PCCD) prepolymers that display a broad range of useful mechanical properties, thermal properties, and shape-memory properties. A novel method for controlling a microscopic and nanoscopic topographical shape-memory phenomenon is presented. Finally, the synthesis of amine-functionalized polyesters is presented. All materials are characterized by 1H and 13C NMR, GPC, DSC, TGA, and Instron.

  10. Mechanical Characterization of Cotton Fiber/Polyester Composite Material

    Directory of Open Access Journals (Sweden)

    Altaf Hussain Rajper

    2014-04-01

    Full Text Available Development of composite from natural fiber for lower structural application is growing for long-term sustainable perspective. Cotton fiber composite material has the added advantages of high specific strength, corrosion resistance, low cost and low weight compared to glass fiber on the expense of internal components of IC engines. The primary aim of the research study is to examine the effect of the cotton fiber on mechanical properties of lower structural applications when added with the polyester resin. In this paper composite material sample has been prepared by hand Lay-Up process. A mould is locally developed in the laboratory for test sample preparation. Initially samples of polyester resin with appropriate ratio of the hardener were developed and tested. At the second stage yarns of cotton fiber were mixed with the polyester resin and sample specimens were developed and tested. Relative effect of the cotton as reinforcing agent was examined and observed that developed composite specimen possess significant improvement in mechanical properties such as tensile strength was improved as 19.78 % and modulus of elasticity was increased up to 24.81%. Through this research it was also observed that developed composite material was of ductile nature and its density decreases up to 2.6%. Results from this study were compared with relevant available advanced composite materials and found improved mechanical properties of developed composite material

  11. Corrosion inhibition property of polyester-groundnut shell biodegradable composite.

    Science.gov (United States)

    Sounthari, P; Kiruthika, A; Saranya, J; Parameswari, K; Chitra, S

    2016-12-01

    The use of natural fibers as reinforcing materials in thermoplastics and thermoset matrix composites provide optimistic environmental profits with regard to ultimate disposability and better use of raw materials. The present work is focused on the corrosion inhibition property of a polymer matrix composite produced by the use of groundnut shell (GNS) waste. Polyester (PE) was synthesized by condensation polymerization of symmetrical 1,3,4-oxadiazole and pimelic acid using sodium lauryl sulfate as surfactant. The polyester-groundnut shell composite (PEGNS) was prepared by ultrasonication method. The synthesized polyester-groundnut shell composite was characterized by FT-IR, TGA and XRD analysis. The corrosion inhibitory effect of PEGNS on mild steel in 1M H2SO4 was investigated using gravimetric method, electrochemical impedance spectroscopy, potentiodynamic polarization, atomic absorption spectroscopy and scanning electron microscopy. The results showed that PEGNS inhibited mild steel corrosion in acid solution and indicated that the inhibition efficiency increased with increasing inhibitor concentration and decrease with increasing temperature. The composite inhibited the corrosion of mild steel through adsorption following the Langmuir adsorption isotherm. Changes in the impedance parameters Rt, Cdl, Icorr, Ecorr, ba and bc suggested the adsorption of PEGNS onto the mild steel surface, leading to the formation of protective film.

  12. The effect of autoclave resterilisation on polyester vascular grafts.

    Science.gov (United States)

    Riepe, G; Whiteley, M S; Wente, A; Rogge, A; Schröder, A; Galland, R B; Imig, H

    1999-11-01

    polyester grafts are expensive, single-use items. Some manufacturers of uncoated, woven grafts include instructions for autoclave resterilisation to be performed at the surgeon's own request. Others warn against such manipulation. Theoretically, the glass transition point of polyester at 70-80 degrees C and the possible acceleration of hydrolysis suggest that autoclave resterilisation at 135 degrees C might be a problem. a DeBakey Soft Woven Dacron Vascular Prosthesis (Bard) and a Woven Double Velour Dacron Graft (Meadox) were autoclave-resterilised 0 to 20 times, having been weighed before and after sterilisation. Tactile testing was performed. Mechanical properties were examined by probe puncture and single-filament testing, the surface was examined by scanning electron microscopy and the degree of hydrolysis by infra-red spectroscopy. tactile testing revealed a change of feeling with increasing cycles of resterilisation. Investigation of weight, textile strength, single-filament strength, electron microscopy of the surface and infra-red spectroscopy showed no change of the material. changes felt are presumably a surface phenomenon, not measurably affecting strength or chemistry of material after autoclave resterilisation. We therefore feel that it is safe to use once-autoclave-resterilised surplus uncoated polyester grafts, provided that sterility is guaranteed. Copyright 1999 Harcourt Publishers Ltd.

  13. Electronic Effects of Aluminum Complexes in the Copolymerization of Propylene Oxide with Tricyclic Anhydrides: Access to Well-Defined, Functionalizable Aliphatic Polyesters.

    Science.gov (United States)

    Van Zee, Nathan J; Sanford, Maria J; Coates, Geoffrey W

    2016-03-02

    The synthesis of well-defined and functionalizable aliphatic polyesters remains a key challenge in the advancement of emerging drug delivery and self-assembly technologies. Herein, we investigate the factors that influence the rates of undesirable transesterification and epimerization side reactions at high conversion in the copolymerization of tricyclic anhydrides with excess propylene oxide using aluminum salen catalysts. The structure of the tricyclic anhydride, the molar ratio of the aluminum catalyst to the nucleophilic cocatalyst, and the Lewis acidity of the aluminum catalyst all influence the rates of these side reactions. Optimal catalytic activity and selectivity against these side reactions requires a careful balance of all these factors. Effective suppression of undesirable transesterification and epimerization was achieved even with sterically unhindered monomers using a fluorinated aluminum salph complex with a substoichiometric amount of a nucleophilic cocatalyst. This process can be used to synthesize well-defined block copolymers via a sequential addition strategy.

  14. 近年来阻燃不饱和聚酯树脂的研究进展%Recent advances in research of flame retardant unsaturated polyester resins

    Institute of Scientific and Technical Information of China (English)

    齐双春; 兰丽琴; 张彦; 程海涛

    2011-01-01

    The research advances tor recent years in preparation of flame retardant unsaturated polyester resins (UPR) adding flame retardant containing aluminum, magnesium and phosphours or intumescent flame retardant in UPR and using flame retardant containing phosphours or monomers containing flame retardant elements as reactants were reviewed.%综述了近年来在不饱和聚酯树脂中添加含铝、镁、磷及膨胀型阻燃剂阻燃不饱和聚酯树脂以及以含磷元素的阻燃剂或含阻燃元素的单体为反应物制备阻燃型不饱和聚酯树脂的研究进展.

  15. MtgA Deletion-Triggered Cell Enlargement of Escherichia coli for Enhanced Intracellular Polyester Accumulation.

    Directory of Open Access Journals (Sweden)

    Ryosuke Kadoya

    Full Text Available Bacterial polyester polyhydroxyalkanoates (PHAs have been produced in engineered Escherichia coli, which turned into an efficient and versatile platform by applying metabolic and enzyme engineering approaches. The present study aimed at drawing out the latent potential of this organism using genome-wide mutagenesis. To meet this goal, a transposon-based mutagenesis was carried out on E. coli, which was transformed to produce poly(lactate-co-3-hydroxybutyrate from glucose. A high-throughput screening of polymer-accumulating cells on Nile red-containing plates isolated one mutant that produced 1.8-fold higher quantity of polymer without severe disadvantages in the cell growth and monomer composition of the polymer. The transposon was inserted into the locus within the gene encoding MtgA that takes part, as a non-lethal component, in the formation of the peptidoglycan backbone. Accordingly, the mtgA-deleted strain E. coli JW3175, which was a derivate of superior PHA-producing strain BW25113, was examined for polymer production, and exhibited an enhanced accumulation of the polymer (7.0 g/l compared to the control (5.2 g/l. Interestingly, an enlargement in cell width associated with polymer accumulation was observed in this strain, resulting in a 1.6-fold greater polymer accumulation per cell compared to the control. This result suggests that the increase in volumetric capacity for accumulating intracellular material contributed to the enhanced polymer production. The mtgA deletion should be combined with conventional engineering approaches, and thus, is a promising strategy for improved production of intracellularly accumulated biopolymers.

  16. Comb-shaped polyesters of aliphatic dicarboxylic acids and 2-octadecyl-1,3-propanediol: 1. Synthesis and microstructure

    DEFF Research Database (Denmark)

    Andruzzi, F.; Hvilsted, S.

    1991-01-01

    Comb-shaped polyesters are prepared by polytransesterification of 2-octadecyl-1,3-propanediol and diphenyl suberate, sebacate, dodecanedioate, tetradecanedioate and hexadecanedioate in turn. The developed melt polycondensation procedure generally results in polyesters with intrinsic viscosities i...

  17. 21 CFR 864.7300 - Fibrin monomer paracoagulation test.

    Science.gov (United States)

    2010-04-01

    ... to detect fibrin monomer in the diagnosis of disseminated intravascular coagulation (nonlocalized clotting within a blood vessel) or in the differential diagnosis between disseminated intravascular coagulation and primary fibrinolysis (dissolution of the fibrin in a blood clot). (b) Classification. Class...

  18. PHOTOINDUCED GRAFTING OF ACRYLIC AND ALLYL MONOMERS ON POLYETHYLENE SURFACE

    Institute of Scientific and Technical Information of China (English)

    ZHANG Zhenfeng; HU Xingzhou; YAN Qing

    1995-01-01

    Photoinduced grafting of acrylic and allyl monomers on polyethylene surface was generally studied by using benzophenone (BP) as a photoinitiator. The grafting process was carried out either in vapor-phase or in solution of the monomers. In the vapor-phase reaction with a filter used to cut off the short wavelength UV light, allyl amine is the most reactive of the four monomers used and acrylic amide is comparatively more reactive than acrylic acid and allyl alcohol. Acetone, as a solvent and carrier for initiator and monomers, however, shows its reactivity to participate the reaction. The solution grafting with a filter is much faster than the corresponding vapor-phase reaction, and a fully covered surface by the grafted polymer can be achieved in this way.

  19. PREPARATION AND SURFACE PROPERTIES OF ACRYLIC COPOLYMERS CONTAINING FLUORINATED MONOMERS

    Institute of Scientific and Technical Information of China (English)

    Tai-jiang Gui; Hao Wei; Ying Zhao; Xiu-lin Wang; Du-jin Wang; Duan-fu Xu

    2006-01-01

    A series of copolymers comprising butylmethacrylate, styrene, butylacrylate, hydroxypropyl acrylate and perfluoroalkyl methacrylate were synthesized by the free radical polymerization using BPO as an initiator. The surface property of the copolymer films was subsequently characterized. The contact angle measurements and energy dispersive analysis of X-ray (EDAX) show that the length and content ofperfluoroalkyl side chains in the copolymers are crucial for the preparation of the film with low surface energy. At a given content of fluorinated monomers in the copolymers, the longer the perfluoroalkyl side chain, the larger the water contact angle of the copolymer films will be. On the other hand, the higher the content of fluorinated monomers, the lower the surface energy is. The water contact angle increases with the increase of the fluorinated monomer content and reaches a plateau at 3 wt% of fluorinated monomer content.

  20. Composition of amino acids, fatty acids and dietary fibre monomers ...

    African Journals Online (AJOL)

    Composition of amino acids, fatty acids and dietary fibre monomers in kernels of ... Nuts are rich in protein and essential amino acids, and have a high energy value ... of protein, especially when combined with foods with high lysine content.

  1. Characterizing the sorption of polybrominated diphenyl ethers (PBDEs) to cotton and polyester fabrics under controlled conditions

    Energy Technology Data Exchange (ETDEWEB)

    Saini, Amandeep [Department of Physical and Environmental Sciences, University of Toronto Scarborough, 1265 Military trail, Toronto, ON M1C 1A4 (Canada); Rauert, Cassandra [School of Geography, Earth and Environmental Sciences, University of Birmingham, Birmingham B15 2TT (United Kingdom); Simpson, Myrna J. [Department of Physical and Environmental Sciences, University of Toronto Scarborough, 1265 Military trail, Toronto, ON M1C 1A4 (Canada); Harrad, Stuart [School of Geography, Earth and Environmental Sciences, University of Birmingham, Birmingham B15 2TT (United Kingdom); Diamond, Miriam L., E-mail: miriam.diamond@utoronto.ca [Department of Earth Sciences, 22 Russell Street, University of Toronto, Toronto, ON M5S 3B1 (Canada); Department of Physical and Environmental Sciences, University of Toronto Scarborough, 1265 Military trail, Toronto, ON M1C 1A4 (Canada)

    2016-09-01

    Cotton and polyester, physically and chemically different fabrics, were characterized for sorption of gas-phase polybrominated diphenyl ethers (PBDEs). Scanning electron microscopic (SEM) images and BET specific surface area (BET-SSA) analysis showed cotton's high microsurface area; NMR analysis showed richness of hexose- and aromatic-carbon in cotton and polyester, respectively. Cotton and polyester sorbed similar concentrations of gas-phase PBDEs in chamber studies, when normalized to planar surface area. However, polyester concentrations were 20–50 times greater than cotton when normalized to BET-SSA, greater than the 10 times difference in BET-SSA. The difference in sorption between cotton and polyester is hypothesized to be due to ‘dilution’ due to cotton's large BET-SSA and/or greater affinity of PBDEs for aromatic-rich polyester. Similar fabric-air area normalized distribution coefficients (K'{sub D}, 10{sup 3} to 10{sup 4} m) for cotton and polyester support air-side controlled uptake under non-equilibrium conditions. K'{sub D} values imply that 1 m{sup 2} of cotton or polyester fabrics would sorb gas-phase PBDEs present in 10{sup 3} to 10{sup 4} m{sup 3} of equivalent air volume at room temperature over one week, assuming similar air flow conditions. Sorption of PBDEs to fabrics has implications for their fate indoors and human exposure. - Highlights: • Sorption of gas-phase PBDEs by cotton and polyester fabrics • Similar sorption to cotton and polyester per unit planar surface area • Greater sorption by polyester/BET-SSA; cotton's dilution or polyester’s affinity • 1 m{sup 2} fabric sorbs PBDEs in 10{sup 3} to 10{sup 4} m{sup 3} of equivalent air volume • Clothing likely a large indoor sink of PBDEs and influence human exposure.

  2. Synthesis of Functional Polyethylene Copolymers via Reactive Monomer

    Institute of Scientific and Technical Information of China (English)

    Hua-yi Li; Shu-qing Zhang; Ling-zhi Wang; You-liang Hu

    2005-01-01

    @@ 1Introduction Polyolefins are used widely due to their good performance and low price, but the poor compatibility and adhesion with other materials limits their applications in broader areas. Reactive monomer approach is effective to synthesize functional polyolefins[1]. In this case, olefin is copolymerized with a reactive comonomer to produce reactive intermediary which is then converted to functional group or initiator to initiate graft-from polymerization of polar monomer.

  3. High-resolution structure of a retroviral protease folded as a monomer

    Energy Technology Data Exchange (ETDEWEB)

    Gilski, Miroslaw [A. Mickiewicz University, 60-780 Poznan (Poland); Polish Academy of Sciences, 61-704 Poznan (Poland); Kazmierczyk, Maciej; Krzywda, Szymon [A. Mickiewicz University, 60-780 Poznan (Poland); Zábranská, Helena [Academy of Sciences of the Czech Republic, 166 10 Prague (Czech Republic); Cooper, Seth; Popović, Zoran [University of Washington, Box 352350, Seattle, WA 98195 (United States); Khatib, Firas; DiMaio, Frank; Thompson, James; Baker, David [University of Washington, Box 357350, Seattle, WA 98195 (United States); Pichová, Iva [Academy of Sciences of the Czech Republic, 166 10 Prague (Czech Republic); Jaskolski, Mariusz, E-mail: mariuszj@amu.edu.pl [A. Mickiewicz University, 60-780 Poznan (Poland); Polish Academy of Sciences, 61-704 Poznan (Poland)

    2011-11-01

    The crystal structure of Mason–Pfizer monkey virus protease folded as a monomer has been solved by molecular replacement using a model generated by players of the online game Foldit. The structure shows at high resolution the details of a retroviral protease folded as a monomer which can guide rational design of protease dimerization inhibitors as retroviral drugs. Mason–Pfizer monkey virus (M-PMV), a D-type retrovirus assembling in the cytoplasm, causes simian acquired immunodeficiency syndrome (SAIDS) in rhesus monkeys. Its pepsin-like aspartic protease (retropepsin) is an integral part of the expressed retroviral polyproteins. As in all retroviral life cycles, release and dimerization of the protease (PR) is strictly required for polyprotein processing and virion maturation. Biophysical and NMR studies have indicated that in the absence of substrates or inhibitors M-PMV PR should fold into a stable monomer, but the crystal structure of this protein could not be solved by molecular replacement despite countless attempts. Ultimately, a solution was obtained in mr-rosetta using a model constructed by players of the online protein-folding game Foldit. The structure indeed shows a monomeric protein, with the N- and C-termini completely disordered. On the other hand, the flap loop, which normally gates access to the active site of homodimeric retropepsins, is clearly traceable in the electron density. The flap has an unusual curled shape and a different orientation from both the open and closed states known from dimeric retropepsins. The overall fold of the protein follows the retropepsin canon, but the C{sup α} deviations are large and the active-site ‘DTG’ loop (here NTG) deviates up to 2.7 Å from the standard conformation. This structure of a monomeric retropepsin determined at high resolution (1.6 Å) provides important extra information for the design of dimerization inhibitors that might be developed as drugs for the treatment of retroviral infections

  4. Perturbation of the Monomer-Monomer Interfaces of the Benzoylformate Decarboxylase Tetramer

    Energy Technology Data Exchange (ETDEWEB)

    Andrews, Forest H.; Rogers, Megan P.; Paul, Lake N.; McLeish, Michael J. [IUPUI; (Purdue)

    2014-08-14

    The X-ray structure of benzoylformate decarboxylase (BFDC) from Pseudomonas putida ATCC 12633 shows it to be a tetramer. This was believed to be typical of all thiamin diphosphate-dependent decarboxylases until recently when the structure of KdcA, a branched-chain 2-keto acid decarboxylase from Lactococcus lactis, showed it to be a homodimer. This lent credence to earlier unfolding experiments on pyruvate decarboxylase from Saccharomyces cerevisiae that indicated that it might be active as a dimer. To investigate this possibility in BFDC, we sought to shift the equilibrium toward dimer formation. Point mutations were made in the noncatalytic monomer–monomer interfaces, but these had a minimal effect on both tetramer formation and catalytic activity. Subsequently, the R141E/Y288A/A306F variant was shown by analytical ultracentrifugation to be partially dimeric. It was also found to be catalytically inactive. Further experiments revealed that just two mutations, R141E and A306F, were sufficient to markedly alter the dimer–tetramer equilibrium and to provide an ~450-fold decrease in kcat. Equilibrium denaturation studies suggested that the residual activity was possibly due to the presence of residual tetramer. The structures of the R141E and A306F variants, determined to <1.5 Å resolution, hinted that disruption of the monomer interfaces will be accompanied by movement of a loop containing Leu109 and Leu110. As these residues contribute to the hydrophobicity of the active site and the correct positioning of the substrate, it seems that tetramer formation may well be critical to the catalytic activity of BFDC.

  5. 78 FR 2366 - Certain Polyester Staple Fiber From the People's Republic of China: Final Results of Antidumping...

    Science.gov (United States)

    2013-01-11

    ... International Trade Administration Certain Polyester Staple Fiber From the People's Republic of China: Final... of the antidumping duty order on certain polyester staple fiber (``PSF'') from the People's Republic... Polyester Staple Fiber From the People's Republic of China: Preliminary Results of the Antidumping...

  6. 76 FR 28420 - Certain Polyester Staple Fiber From the People's Republic of China: Full Extension of Preliminary...

    Science.gov (United States)

    2011-05-17

    ... International Trade Administration Certain Polyester Staple Fiber From the People's Republic of China: Full... polyester staple fiber from the People's Republic of China (``PRC''). This review covers the period June 1... duty order on certain polyester staple fiber from the PRC. See Initiation of Antidumping...

  7. 77 FR 54898 - Certain Polyester Staple Fiber From the People's Republic of China: Final Results of Expedited...

    Science.gov (United States)

    2012-09-06

    ... International Trade Administration Certain Polyester Staple Fiber From the People's Republic of China: Final... certain polyester staple fiber from the People's Republic of China (``PRC'') pursuant to section 751(c) of... duty order on certain polyester staple fiber from the PRC would be likely to lead to continuation...

  8. 78 FR 38939 - Certain Polyester Staple Fiber From the People's Republic of China: Final Results of Antidumping...

    Science.gov (United States)

    2013-06-28

    ... International Trade Administration Certain Polyester Staple Fiber From the People's Republic of China: Final... antidumping duty order on certain polyester staple fiber (``PSF'') from the People's Republic of China (``PRC... below. \\1\\ See Certain Polyester Staple Fiber From the People's Republic of China: Preliminary...

  9. 75 FR 5763 - Notice of Correction to the First Administrative Review of Certain Polyester Staple Fiber From...

    Science.gov (United States)

    2010-02-04

    ... International Trade Administration Notice of Correction to the First Administrative Review of Certain Polyester... antidumping duty order on certain polyester staple fiber from the People's Republic of China (``PRC''). See First Administrative Review of Certain Polyester Staple Fiber From the People's Republic of China:...

  10. 75 FR 34097 - Certain Polyester Staple Fiber From Taiwan: Extension of the Final Results of Antidumping Duty...

    Science.gov (United States)

    2010-06-16

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Certain Polyester Staple Fiber From Taiwan: Extension of the Final Results of... certain polyester staple fiber from Taiwan. See Certain Polyester Staple Fiber from Taiwan:...

  11. 76 FR 38612 - Certain Polyester Staple Fiber From the Republic of Korea and Taiwan: Final Results of the...

    Science.gov (United States)

    2011-07-01

    ... International Trade Administration Certain Polyester Staple Fiber From the Republic of Korea and Taiwan: Final... Commerce (the Department) initiated the second sunset reviews of the antidumping duty orders on polyester... otherwise processed for spinning, of polyesters measuring 3.3 decitex (3 denier, inclusive) or more...

  12. 76 FR 60802 - Certain Polyester Staple Fiber From the Republic of Korea and Taiwan: Continuation of Antidumping...

    Science.gov (United States)

    2011-09-30

    ... International Trade Administration Certain Polyester Staple Fiber From the Republic of Korea and Taiwan... certain polyester staple fiber from the Republic of Korea (Korea) and Taiwan would likely lead to a... orders on polyester staple fiber from Korea and Taiwan \\1\\ pursuant to section 751(c) of the Tariff...

  13. 75 FR 76954 - Certain Polyester Staple Fiber From the People's Republic of China: Extension of Time Limit for...

    Science.gov (United States)

    2010-12-10

    ... International Trade Administration Certain Polyester Staple Fiber From the People's Republic of China: Extension... Register the Preliminary Results of the second administrative review of certain polyester staple fiber.... See Certain Polyester Staple Fiber From the People's Republic of China: Notice of Preliminary...

  14. 76 FR 37830 - Polyester Staple Fiber From Korea and Taiwan; Scheduling of Expedited Five-Year Reviews...

    Science.gov (United States)

    2011-06-28

    ... COMMISSION Polyester Staple Fiber From Korea and Taiwan; Scheduling of Expedited Five-Year Reviews Concerning the Antidumping Duty Orders on Polyester Staple Fiber From Korea and Taiwan AGENCY: United States...) to determine whether revocation of the antidumping duty orders on polyester staple fiber from...

  15. 77 FR 21733 - Certain Polyester Staple Fiber From Taiwan: Extension of Time Limit for Preliminary Results of...

    Science.gov (United States)

    2012-04-11

    ... International Trade Administration Certain Polyester Staple Fiber From Taiwan: Extension of Time Limit for... antidumping duty order on certain polyester staple fiber from Taiwan for the period May 1, 2010, through April 30, 2011.\\1\\ In Certain Polyester Staple Fiber From Taiwan: Extension of Time Limit for...

  16. 75 FR 64252 - Certain Polyester Staple Fiber From the Republic of Korea: Final Results of the 2008-2009...

    Science.gov (United States)

    2010-10-19

    ... International Trade Administration Certain Polyester Staple Fiber From the Republic of Korea: Final Results of... certain polyester staple fiber from the Republic of Korea and invited interested parties to comment. The... 15, 2010, the Department of Commerce (``the Department'') published Certain Polyester Staple...

  17. 76 FR 2886 - Certain Polyester Staple Fiber From the People's Republic of China: Final Results and Partial...

    Science.gov (United States)

    2011-01-18

    ... International Trade Administration Certain Polyester Staple Fiber From the People's Republic of China: Final... second administrative review of the antidumping duty order on certain polyester staple fiber (``PSF'') from the People's Republic of China (``PRC''). See Certain Polyester Staple Fiber From the...

  18. 77 FR 50530 - Polyester Staple Fiber From China; Scheduling of an Expedited Five-Year Review Concerning the...

    Science.gov (United States)

    2012-08-21

    ... COMMISSION Polyester Staple Fiber From China; Scheduling of an Expedited Five-Year Review Concerning the Antidumping Duty Order on Polyester Staple Fiber From China AGENCY: United States International Trade... determine ] whether revocation of the antidumping duty order on polyester staple fiber from China would...

  19. 77 FR 71579 - Polyester Staple Fiber From Taiwan: Notice of Court Decision Not in Harmony With Final Results of...

    Science.gov (United States)

    2012-12-03

    ... International Trade Administration Polyester Staple Fiber From Taiwan: Notice of Court Decision Not in Harmony... order on polyester staple fiber from Taiwan covering the period of review (``POR'') May 1, 2009, through... Certain Polyester Staple Fiber From Taiwan: Final Results of Antidumping Duty Administrative Review, 76...

  20. 75 FR 38463 - Greige Polyester Cotton Printcloth From the People's Republic of China: Final Results of Sunset...

    Science.gov (United States)

    2010-07-02

    ... International Trade Administration Greige Polyester Cotton Printcloth From the People's Republic of China: Final... Order; Greige Polyester Cotton Printcloth from the People's Republic of China, 70 FR 36927 (June 27... Antidumping Duty Order; Greige Polyester Cotton Printcloth from the People's Republic of China, 70 FR...

  1. 76 FR 52935 - Certain Polyester Staple Fiber From Korea: Rescission of Antidumping Duty Administrative Review

    Science.gov (United States)

    2011-08-24

    ... International Trade Administration Certain Polyester Staple Fiber From Korea: Rescission of Antidumping Duty... to request an administrative review of the antidumping order on polyester staple fiber from Korea... Reviews and Request for Revocation in Part, 76 FR 37781 (June 28, 2011). Scope of the Order...

  2. Incorporation of different crystallizable amide blocks in segmented poly(ester amide)s

    NARCIS (Netherlands)

    Lips, P.A.M.; Broos, R.; Heeringen, van M.J.M.; Dijkstra, P.J.; Feijen, J.

    2005-01-01

    High molecular weight segmented poly(ester amide)s were prepared by melt polycondensation of dimethyl adipate, 1,4-butanediol and a symmetrical bisamide-diol based on ε-caprolactone and 1,2-diaminoethane or 1,4-diaminobutane. FT-IR and WAXD analysis revealed that segmented poly(ester amide)s based

  3. Prevention of primary vascular graft infection with silver-coated polyester graft in a porcine model

    DEFF Research Database (Denmark)

    Gao, H; Sandermann, J; Prag, J;

    2010-01-01

    To evaluate the efficacy of a silver-coated vascular polyester graft in the prevention of graft infection after inoculation with Staphylococcus aureus in a porcine model.......To evaluate the efficacy of a silver-coated vascular polyester graft in the prevention of graft infection after inoculation with Staphylococcus aureus in a porcine model....

  4. Light-induced circular birefringence in cyanoazobenzene side-chain liquid-crystalline polyester films

    DEFF Research Database (Denmark)

    Naydenova, I; Nikolova, L; Ramanujam, P.S.;

    1999-01-01

    We report the inducement of large circular birefringence (optical activity) in films of a cyanoazobenzene side-chain liquid-crystalline polyester on illumination with circularly polarized light. The polyester has no chiral groups and is initially isotropic. The induced optical rotation is up to 5...

  5. Life-cycle assessment of textiles manufacture of polyester shirt (VB)

    DEFF Research Database (Denmark)

    Othman, Samer; Peter, Oduro Justice; Hassan, Osama;

    1998-01-01

    According to the EDIP (Environmental Design of Industrial Products), It is made possible to perform resource and environmental profile analysis of the 100% polyester shirt. In order to understand the true life-cycle consequences, life-cycle analysis of a typical 100% polyester shirt was carried out...

  6. Techno-economic analysis of unsaturated polyester production from waste PET

    OpenAIRE

    Drah, Abdusalam; Rusmirović, Jelena D.; Milošević, Milena; Kalifa, Mustafa; Stojiljković, Ivana; Rančić, Milica; Aleksandar D. Marinković

    2016-01-01

    Unsaturated polyester resins (UPe) were synthesized from maleic anhydride and products of glycolysis, obtained by polyethylene terephthalate (PET) depolymerization with dipropylene glycol (DPG) in the presence of tetrabutyl titanate catalyst. Waste PET glycolyzed product and UPes were characterized by FTIR and NMR spectroscopy, elemental analysis, acid value (AV), hydroxyl value (HV) and iodine value. Nanocomposites, based on unsaturated polyester resins and hexamethyldisilazane modified sili...

  7. Azobenzene side-chain liquid crystalline polyesters with outstanding optical storage properties

    DEFF Research Database (Denmark)

    Hvilsted, Søren; Pedersen, M; Holme, NCR

    1998-01-01

    on azobenzene, iii- the methylene main-chain segment length, and iv-the polyester molecular mass, all influence the optical storage properties. A general synthetic route to novel mesogenic azobenzene diols comprising parameters i and ii is outlined. Polyesters with molecular masses (parameter iv) up to 100...

  8. 含光敏剂的高支化碱溶性感光聚合物的合成及性能%SYNTHESIS AND PHOTOCURING OF HIGHLY BRANCHED ACRYLATED POLYESTERS CONTAINING PHOTOINITIATOR

    Institute of Scientific and Technical Information of China (English)

    冯宗财; 王跃川; 赵凌

    2001-01-01

    以1,2,4-苯三甲酸酐、环氧氯丙烷和光敏剂1173合成了分子内带有光敏单元的高支化碱溶性聚酯,聚合反应转化率在1 h内可达90%以上;以甲基丙烯酸缩水甘油酯与高支化聚酯反应制得分子内带有光敏单元的高支化碱溶性光固化树脂;树脂的热转变温度在160~210 ℃,在碱水溶液中溶解性好,无需外加光敏剂在紫外光照射下便可固化、交联,光固化的反差γ可达到7.30。%Highly branched acrylated polyesters containing photoinitiator were synthesized from 1,2,4-trimellitic anhydride, epichlorohydrin and glycidyl methacrylate and photoinititor 1173. Conversions of monomers to the aqueous soluble polyesters were over 90% within one hour. The acrylated polyesters were obtained by the reaction of aqueous soluble polyesters with glycidyl methacrylate. These resins were aqueous soluble, showed thermal transition at 160~210 ℃, and could be photocured by UV irradiation without additional photoinitiators. Photocuring of these resins were studied with sensitivity E0 40~160 mJ/cm2, and contract value γ 1.4~7.

  9. Synthesis of unsaturated polyesters for improved interfacial strength in carbon fibre composites

    DEFF Research Database (Denmark)

    Gamstedt, E.K.; Skrifvars, M.; Jacobsen, T. K.

    2002-01-01

    Carbon fibres are gaining use as reinforcement in glass fibre/polyester composites for increased stiffness as a hybrid composite. The mechanics and chemistry of the carbon fibre–polyester interface should be addressed to achieve an improvement also in fatigue performance and off-axis strength....... To make better use of the versatility of unsaturated polyesters in a carbon fibre composite, a set of unsaturated polyester resins have been synthesized with different ratios of maleic anhydride, o-phthalic anhydride and 1,2-propylene glycol as precursors. The effective interfacial strength was determined...... by micro-Raman spectroscopy of a single-fibre composite tested in tension. The interfacial shear strength with untreated carbon fibres increased with increasing degree of unsaturation of the polyester, which is controlled by the relative amount of maleic anhydride. This can be explained by a contribution...

  10. Flame Retardance and Physical Properties of Novel Cured Blends of Unsaturated Polyester and Furan Resins

    Directory of Open Access Journals (Sweden)

    Baljinder Kaur Kandola

    2015-02-01

    Full Text Available Novel blends of two furan resins with an unsaturated polyester have been prepared and cured by parallel free radical (for the unsaturated polyester and acid-catalysed crosslinking (for the furan resin to give co-cured composite materials. Although these materials have inferior physical properties, such as low Tg and low storage modulus compared with those of unsaturated polyester and furan resins alone, they show markedly improved flame retardance compared with that of the normally highly flammable unsaturated polyester. This increased flame retardance arises from a condensed phase mechanism in which the furanic component forms a semi-protective char, reducing rates of thermal degradation and total heat release and heat of combustion. The blends also burn with reduced smoke output compared with that from unsaturated polyester alone.

  11. Biodegradation of polyester polyurethane during commercial composting and analysis of associated fungal communities.

    Science.gov (United States)

    Zafar, Urooj; Nzeram, Petrus; Langarica-Fuentes, Adrian; Houlden, Ashley; Heyworth, Alan; Saiani, Alberto; Robson, Geoff D

    2014-04-01

    In this study the biodegradation of polyurethane (PU) during the maturation stage of a commercial composting process was investigated. PU coupons were buried in the centre and at the surface of a 10 m high compost pile. Fungal communities colonising polyester PU coupons were compared with the native compost communities using culture based and molecular techniques. Putative polyester PU degrading fungi were ubiquitous in compost and rapidly colonised the surface of polyester PU coupons with significant deterioration. As the temperature decreased, fungal diversity in the compost and on the surface of the polyester PU coupons increased and selection of fungal community on the polyester PU coupons occurs that is different from the surrounding compost. Copyright © 2014 Elsevier Ltd. All rights reserved.

  12. Enzymatic saccharification coupling with polyester recovery from cotton-based waste textiles by phosphoric acid pretreatment.

    Science.gov (United States)

    Shen, Fei; Xiao, Wenxiong; Lin, Lili; Yang, Gang; Zhang, Yanzong; Deng, Shihuai

    2013-02-01

    In order to recycle the cotton-based waste textiles, a novel process was designed for pretreating waste textiles with phosphoric acid to recover polyester and fermentable sugar. The effects of pretreatment conditions including, phosphoric acid concentration, pretreatment temperature, time, and ratio of textiles and phosphoric acid were thoroughly investigated. Results indicated the mentioned four factors had significant influences on sugar and polyester recovery. Almost complete polyester recovery was achieved by enhancing phosphoric acid concentration, temperature and pretreatment time or reducing the ratio of textiles and phosphoric acid. However, these behaviors decreased the sugar recovery seriously. 100% polyester recovery with a maximum sugar recovery of 79.2% was achieved at the optimized conditions (85% phosphoric acid, 50°C, 7h, and the ratio of 1:15). According to the technical and cost-benefit analysis, it was technically feasible and potentially profitable to recover polyester and sugar from waste textiles by phosphoric acid pretreatment.

  13. Fungal Communities Associated with Degradation of Polyester Polyurethane in Soil▿

    OpenAIRE

    Cosgrove, Lee; McGeechan, Paula L.; Robson, Geoff D.; Handley, Pauline S.

    2007-01-01

    Soil fungal communities involved in the biodegradation of polyester polyurethane (PU) were investigated. PU coupons were buried in two sandy loam soils with different levels of organic carbon: one was acidic (pH 5.5), and the other was more neutral (pH 6.7). After 5 months of burial, the fungal communities on the surface of the PU were compared with the native soil communities using culture-based and molecular techniques. Putative PU-degrading fungi were common in both soils, as 80% of cultiv...

  14. Mechanical and Morphological Properties of Nano Filler Polyester Composites

    OpenAIRE

    Bonnia Noor Najmi; Redzuan Aein Afina; Shuhaimeen Nurul Shakirah

    2016-01-01

    This research is focusing on mechanical and morphological properties of unsaturated polyester (UP) reinforced with two different types of filler which is nano size clay Cloisite 30B (C30B) and Carbon Black (CB). Samples were fabricated via hand lay-up and open molding technique. Percentages of Cloisite 30B & Carbon Black (CB) used vary from 0, 2, 4, 6, 8 and 10 wt%. The mechanical properties were evaluated by impact, flexural and hardness testing. Result shows that the mechanical strength of ...

  15. Bending Mechanical Behavior of Polyester Matrix Reinforced with Fique Fiber

    Science.gov (United States)

    Altoé, Giulio Rodrigues; Netto, Pedro Amoy; Barcelos, Mariana; Gomes, André; Margem, Frederico Muylaert; Monteiro, Sergio Neves

    Environmentally correct composites, made from natural fibers, are among the most investigated and applied today. In this paper, we investigate the mechanical behavior of polyester matrix composites reinforced with continuous fique fibers, through bending tensile tests. Specimens containing 0, 10, 20 and 30% in volume of fique fiber were aligned along the entire length of a mold to create plates of these composites, those plates were cut following the ASTM standard to obtained bending tests specimens. The test was conducted in a Instron Machine and the fractured specimens were analyzed by SEM, the results showed the increase in the materials tensile properties with the increase of fiber amount.

  16. Post-irradiation crosslinking of partially cured unsaturated polyester resin

    Energy Technology Data Exchange (ETDEWEB)

    Jurkin, Tanja [Ruder Boskovic Institute, POB 180, Zagreb (Croatia); Pucic, Irina [Ruder Boskovic Institute, POB 180, Zagreb (Croatia)]. E-mail: pucic@rudjer.irb.hr

    2006-09-15

    The post-irradiation crosslinking of unsaturated polyester (UP) resin samples irradiated to different doses was monitored during the 15-days period. The post-reaction sensitivity of three experimental techniques was evaluated. Significant changes were detected by extraction analysis that also included determination of the free styrene content. The most substantial changes were detected by differential scanning calorimetry, even up to 5 days after the irradiation. The sensitivity and reproducibility of FTIR was the lowest. The first two techniques detected the influence of particular reaction periods, at which the radiation crosslinking was terminated, on the post-reaction.

  17. Post-irradiation crosslinking of partially cured unsaturated polyester resin

    Science.gov (United States)

    Jurkin, Tanja; Pucić, Irina

    2006-09-01

    The post-irradiation crosslinking of unsaturated polyester (UP) resin samples irradiated to different doses was monitored during the 15-days period. The post-reaction sensitivity of three experimental techniques was evaluated. Significant changes were detected by extraction analysis that also included determination of the free styrene content. The most substantial changes were detected by differential scanning calorimetry, even up to 5 days after the irradiation. The sensitivity and reproducibility of FTIR was the lowest. The first two techniques detected the influence of particular reaction periods, at which the radiation crosslinking was terminated, on the post-reaction.

  18. Thiophene based monoazo disperse dyes for polyester fabric

    Directory of Open Access Journals (Sweden)

    VITHAL SOMA PATEL

    2002-01-01

    Full Text Available A series of monoazo disperse dyes have been prepared by coupling 2-amino-3-carbethoxy-4,5-dimethylthiophene with various N-arylmaleimides. The monoazo disperse dyes were characterised by IR spectral studies and elemental analysis. These dyes were applied at 2 % depth on polyester fabrics and gave light yellow to brown colour hues with fair fastness to light and very good to excellent fastness to washing, rubbing, perspiration and sublimation. The percentage exhaustion of the dyebath and fixation on the fabric were found to be very good.

  19. Comparative study on adhesive performance of functional monomers.

    Science.gov (United States)

    Yoshida, Y; Nagakane, K; Fukuda, R; Nakayama, Y; Okazaki, M; Shintani, H; Inoue, S; Tagawa, Y; Suzuki, K; De Munck, J; Van Meerbeek, B

    2004-06-01

    Mild self-etch adhesives demineralize dentin only partially, leaving hydroxyapatite around collagen within a submicron hybrid layer. We hypothesized that this residual hydroxyapatite may serve as a receptor for chemical interaction with the functional monomer and, subsequently, contribute to adhesive performance in addition to micro-mechanical hybridization. We therefore chemically characterized the adhesive interaction of 3 functional monomers with synthetic hydroxyapatite, using x-ray photoelectron spectroscopy and atomic absorption spectrophotometry. We further characterized their interaction with dentin ultra-morphologically, using transmission electron microscopy. The monomer 10-methacryloxydecyl dihydrogen phosphate (10-MDP) readily adhered to hydroxyapatite. This bond appeared very stable, as confirmed by the low dissolution rate of its calcium salt in water. The bonding potential of 4-methacryloxyethyl trimellitic acid (4-MET) was substantially lower. The monomer 2-methacryloxyethyl phenyl hydrogen phosphate (phenyl-P) and its bond to hydroxyapatite did not appear to be hydrolytically stable. Besides self-etching dentin, specific functional monomers have additional chemical bonding efficacy that is expected to contribute to their adhesive potential to tooth tissue.

  20. Synthesis and characterization of polyester thin film composite membrane via interfacial polymerization: Fouling behaviour of uncharged solute

    Science.gov (United States)

    Mah, K. H.; Yussof, H. W.; Seman, M. N. A.; Mohammad, A. W.

    2016-11-01

    Most hydrolysis studies on biomass in Malaysia produce high amount of xylose and glucose compared to other monosaccharides and most of them are acidic. Thin film composite (TFC) membrane developed via interfacial polymerization using triethanolamine (TEOA) and trimesoyl chloride (TMC) as monomers allows separation at low pH to occur without damaging its performance. Comparative studies were carried out on membranes with and without the thin film layer formed via interfacial polymerization on the polyethersulfone (PES) support. The surfaces of the membranes were characterized by field emission scanning electronic microscopy (FESEM), attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy, and hydrophilicity via contact angle measurement. In addition, the performance and uncharged solute fouling behaviour of TFC membrane were also investigated. The TFC membrane used for characterization purposes was prepared at TEOA concentration of 4 % w/v in 1 × 10-6 M sodium hydroxide solution, TMC concentration of 0.25 % w/v in pure hexane, reaction time of 45 minutes, and cured at temperature of 60 °C. Characterization results showed a huge different between the synthesized TFC membrane and the un-synthesized PES membrane in term of surface properties and morphology. Nanofiltration results indicate that the formation of thin layer on top of PES support membrane improved the separation performance compared to PES support membrane. The synthesised polyester TFC membrane have irreversible fouling of 11.02 (±5.60) % and reversible fouling of 5.59 % using water as cleaning agent.

  1. Synthesis of Cu/SiO2 Core-Shell Particles Using Hyperbranched Polyester as Template and Dispersant

    Science.gov (United States)

    Han, Wensong

    2017-07-01

    Third-generation hyperbranched polyester (HBPE3) was synthesized by stepwise polymerization with N, N-diethylol-3-amine methylpropionate as AB2 monomer and pentaerythritol as core molecule. Then, Cu particles were prepared by reduction of copper nitrate with ascorbic acid in aqueous solution using HBPE3 as template. Finally, Cu/SiO2 particles were prepared by coating silica on the surface of Cu particles. The structure and morphology of the samples were characterized by Fourier-transform infrared (FT-IR) spectrometry, x-ray diffraction (XRD) analysis, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). The results confirmed the formation of the silica coating on the surface of Cu and that the Cu/SiO2 particles had spherical shape with particle size in the range of 0.8 μm to 2 μm. Compared with pure Cu, the synthesized Cu/SiO2 core-shell particles exhibited better oxidation resistance at high temperature. Moreover, the oxidation resistance of the Cu/SiO2 particles increased significantly with increasing tetraethyl orthosilicate (TEOS) concentration.

  2. Synthesis of High Solid Polyester Resin%高固体分聚酯树脂的合成

    Institute of Scientific and Technical Information of China (English)

    晏莉

    2011-01-01

    A high solid polyester resin was synthesized by polybasic acid and polyols using melting condensation reaction. The synthetic products were characterized by Fourier transform infrared spectrometry ( FTIR ) and gel permeation chromatography ( GPC ). The effects of monomers, the molar ratio of alcohol and acid, reaction temperature, reaction time and charging method on the performance of the synthetic products were researched.%以多元酸和多元醇为反应单体,采用熔融缩聚的方法合成了高固体分聚酯树脂。对合成产物进行了傅里叶变换红外光谱(FTIR)和凝胶渗透色谱(GPC)等表征。研究了反应单体、n醇/n酸、反应温度、反应时间、加料方法对合成产物性能的影响。

  3. OGP functionalized phenylalanine-based poly(ester urea) for enhancing osteoinductive potential of human mesenchymal stem cells.

    Science.gov (United States)

    Policastro, Gina M; Lin, Fei; Smith Callahan, Laura A; Esterle, Andrew; Graham, Matthew; Sloan Stakleff, Kimberly; Becker, Matthew L

    2015-04-13

    Amino acid-based poly(ester urea)s (PEU) are high modulus, resorbable polymers with many potential uses, including the surgical repair of bone defects. In vitro and in vivo studies have previously shown that phenylalanine-based PEUs have nontoxic hydrolytic byproducts and tunable degradation times. Phenylalanine PEUs (poly(1-PHE-6)) have been further modified by tethering osteogenic growth peptide (OGP) to tyrosine-based monomer subunits. These OGP-tethered PEUs have been fabricated into porous scaffolds and cultured in vitro to examine their effect on differentiation of human mesenchymal stem cells (hMSCs) toward the osteogenic lineage. The influence of tethered OGP on the hMSC proliferation and differentiation profile was measured using immunohistochemistry, biochemistry, and quantitative real time polymerase chain reaction (qRT-PCR). In vitro data indicated an enhanced expression of BSP by 130-160% for hMSCs on OGP-tethered scaffolds compared to controls. By 4 weeks, there was a significant drop (60-85% decrease) in BSP expression on OGP-functionalized scaffolds, which is characteristic of osteogenic differentiation. ALP and OSC expression was significantly enhanced for OGP-functionalized scaffolds by week 4, with values reaching 145% and 300% greater, respectively, compared to nonfunctionalized controls. In vivo subcutaneous implantation of poly(1-PHE-6) scaffolds revealed significant tissue-scaffold integration, as well as the promotion of both osteogenesis and angiogenesis.

  4. Abaca/polyester nonwoven fabric functionalization for metal ion adsorbent synthesis via electron beam-induced emulsion grafting

    Science.gov (United States)

    Madrid, Jordan F.; Ueki, Yuji; Seko, Noriaki

    2013-09-01

    A metal ion adsorbent was developed from a nonwoven fabric trunk material composed of both natural and synthetic polymers. A pre-irradiation technique was used for emulsion grafting of glycidyl methacrylate (GMA) onto an electron beam irradiated abaca/polyester nonwoven fabric (APNWF). The dependence of degree of grafting (Dg), calculated from the weight of APNWF before and after grafting, on absorbed dose, reaction time and monomer concentration were evaluated. After 50 kGy irradiation with 2 MeV electron beam and subsequent 3 h reaction with an emulsion consisting of 5% GMA and 0.5% polyoxyethylene sorbitan monolaurate (Tween 20) surfactant in deionized water at 40 °C, a grafted APNWF with a Dg greater than 150% was obtained. The GMA-grafted APNWF was further modified by reaction with ethylenediamine (EDA) in isopropyl alcohol at 60 °C to introduce amine functional groups. After a 3 h reaction with 50% EDA, an amine group density of 2.7 mmole/gram adsorbent was achieved based from elemental analysis. Batch adsorption experiments were performed using Cu2+ and Ni2+ ions in aqueous solutions with initial pH of 5 at 30 °C. Results show that the adsorption capacity of the grafted adsorbent for Cu2+ is four times higher than Ni2+ ions.

  5. 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.

  6. The limits of precision monomer placement in chain growth polymerization

    Science.gov (United States)

    Gody, Guillaume; Zetterlund, Per B.; Perrier, Sébastien; Harrisson, Simon

    2016-02-01

    Precise control over the location of monomers in a polymer chain has been described as the `Holy Grail' of polymer synthesis. Controlled chain growth polymerization techniques have brought this goal closer, allowing the preparation of multiblock copolymers with ordered sequences of functional monomers. Such structures have promising applications ranging from medicine to materials engineering. Here we show, however, that the statistical nature of chain growth polymerization places strong limits on the control that can be obtained. We demonstrate that monomer locations are distributed according to surprisingly simple laws related to the Poisson or beta distributions. The degree of control is quantified in terms of the yield of the desired structure and the standard deviation of the appropriate distribution, allowing comparison between different synthetic techniques. This analysis establishes experimental requirements for the design of polymeric chains with controlled sequence of functionalities, which balance precise control of structure with simplicity of synthesis.

  7. Monomer release from nanofilled and microhybrid dental composites after bleaching.

    Directory of Open Access Journals (Sweden)

    Masumeh Hasani Tabatabaee

    2014-02-01

    Full Text Available The aim of this study was to assess the effect of bleaching on elution of monomers from nanofilled and microhybrid composites.80 samples (5mm diameter and 3mm thickness of each composite were prepared. After curing, half of them were randomly polished. Each group was divided into 8 subgroups and immersed in water or 10%, 20% and 30% H2O2 for 3 or 8 hours. Eluted Bis-GMA (Bis-phenol A Glycidyl Dimethacrylate, TEGDMA (Triethyleneglycol Dimethacrylate, UDMA (Urethane Dimethacrylate and BisEMA (Bis-phenol A ethoxylate Dimethacrylate were quantified by high performance liquid chromatography and the results were analyzed by univariate ANOVA and t-test (P<0.05.Bleach significantly increased the overall release of monomers (P<0.001; TEGDMA was released more than Bis-GMA (P<0.001. Supreme released more TEGDMA compared to Z250 (P<0.001. Bleaching increased the release of this monomer (P<0.001. Increasing both the concentration of H2O2, and the immersion time, increased the release of TEGDMA (P<0.001. Polishing had no effect on release of this monomer (P=0.952. Supreme released more Bis-GMA than Z250 (P=0.000. The more concentrated H2O2 caused more elution of Bis-GMA (P= 0.003; while the effect of immersion time was not significant (P=0.824. Polishing increased the release of Bis-GMA (P=0.001. Neither the type of composite nor Bleaching had any effect on release of UDMA (P=0.972 and (P=0.811 respectively. Immersion duration increased the release of UDMA (P=0.002, as well as polishing (P=0.024.Bleaching increased the release of monomers. Nanofilled composites released more monomer than the microfilled.

  8. The Quest for Converting Biorenewable Bifunctional α-Methylene-γ-butyrolactone into Degradable and Recyclable Polyester: Controlling Vinyl-Addition/Ring-Opening/Cross-Linking Pathways

    KAUST Repository

    Tang, Xiaoyan

    2016-10-04

    α-Methylene-γ-butyrolactone (MBL), a naturally occurring and biomass-sourced bifunctional monomer, contains both a highly reactive exocyclic C═C bond and a highly stable five-membered γ-butyrolactone ring. Thus, all previous work led to exclusive vinyl-addition polymerization (VAP) product P(MBL)VAP. Now, this work reverses this conventional chemoselectivity to enable the first ring-opening polymerization (ROP) of MBL, thereby producing exclusively unsaturated polyester P(MBL)ROP with Mn up to 21.0 kg/mol. This elusive goal was achieved through uncovering the thermodynamic, catalytic, and processing conditions. A third reaction pathway has also been discovered, which is a crossover propagation between VAP and ROP processes, thus affording cross-linked polymer P(MBL)CLP. The formation of the three types of polymers, P(MBL)VAP, P(MBL)CLP, and P(MBL)ROP, can be readily controlled by adjusting the catalyst (La)/initiator (ROH) ratio, which is determined by the unique chemoselectivity of the La–X (X = OR, NR2, R) group. The resulting P(MBL)ROP is degradable and can be readily postfunctionalized into cross-linked or thiolated materials but, more remarkably, can also be fully recycled back to its monomer thermochemically. Computational studies provided the theoretical basis for, and a mechanistic understanding of, the three different polymerization processes and the origin of the chemoselectivity.

  9. Micropatterned coumarin polyester thin films direct neurite orientation.

    Science.gov (United States)

    McCormick, Aleesha M; Maddipatla, Murthy V S N; Shi, Shuojia; Chamsaz, Elaheh A; Yokoyama, Hiroshi; Joy, Abraham; Leipzig, Nic D

    2014-11-26

    Guidance and migration of cells in the nervous system is imperative for proper development, maturation, and regeneration. In the peripheral nervous system (PNS), it is challenging for axons to bridge critical-sized injury defects to achieve repair and the central nervous system (CNS) has a very limited ability to regenerate after injury because of its innate injury response. The photoreactivity of the coumarin polyester used in this study enables efficient micropatterning using a custom digital micromirror device (DMD) and has been previously shown to be biodegradable, making these thin films ideal for cell guidance substrates with potential for future in vivo applications. With DMD, we fabricated coumarin polyester thin films into 10×20 μm and 15×50 μm micropatterns with depths ranging from 15 to 20 nm to enhance nervous system cell alignment. Adult primary neurons, oligodendrocytes, and astrocytes were isolated from rat brain tissue and seeded onto the polymer surfaces. After 24 h, cell type and neurite alignment were analyzed using phase contrast and fluorescence imaging. There was a significant difference (ppolyester thin films has proven beneficial as an axon guidance platform for future nervous system regenerative strategies.

  10. Sponge Gourd (Luffa Cylindrica Reinforced Polyester Composites: Preparation and Properties

    Directory of Open Access Journals (Sweden)

    Valcineide O.A. Tanobe

    2014-05-01

    Full Text Available Increasing environmental concern along with the drive to find substitutes for synthetic fibers and value added applications for low cost and renewable plant fibers have led to the development of composites based on biomaterials. One of the drawbacks encountered in such exercise is the lack of adhesion between the incorporated plant fibers and synthetic polymeric matrices. Such drawback can be reduced by appropriate treatment of fibers. This paper describes the chemical treatments used on sponge gourd (Luffa cylindrica fibers of Brazil to prepare their composites with polyester resin. Production of short fiber-polymer composite as well as mat-polyester composites is presented here. Characterization of the composites in respect of evaluation of density, water absorption, thermalstability, tensile properties and impact strength were made and the results are discussed. Observed impact strengthand tensile properties are discussed based on the fractographic studies of the composites.Defence Science Journal, Vol. 64, No. 3, May 2014, pp. 273-280, DOI:http://dx.doi.org/ 10.14429/dsj.64.7327

  11. MICROWAVE RADIATIONS FOR HEAT-SETTING OF POLYESTER FIBERS

    Directory of Open Access Journals (Sweden)

    Ajit V.Gore

    2009-12-01

    Full Text Available The use of radio and microwave frequency is gainingimportance for industrial applications such asheating, drying, and other processing. The mostimportant advantage of using microwave is that it isnon-contact or localized heating and the heat isproduced within the material. This can be much moreeffective than indirect heating where the heatpropagation is by heat conduction through thematerial. We have been investigating the influence ofmicrowave radiation on different fibers for the lastfew years. In the present investigation we usedmicrowave frequency of 2450 MHz to investigate itseffect on polyester fibers. The polyester fibers wereheat set in air as well as a liquid, which acted as alossy substances. The liquid was chosen on the basisof earlier experiments, which showed the maximumeffect. A comparative study was also carried outusing conventional heating in silicone oil.Using the method of X-ray Diffraction (XRD wecalculated the changes in % crystallinity andorientation. It was found that as the time of treatmentunder microwave radiation increased from 15 sec. to120 sec. the order factor was found to increase from0.32 to 0.71.The crystalline orientation as determinedfrom the azimuthal scan was also found to increase.Such structural changes can be highly beneficial forthe processing of fabric in industry. The microwaveradiation process is fast, reliable and energy saving.

  12. Glass fibres reinforced polyester composites degradation monitoring by surface analysis

    Energy Technology Data Exchange (ETDEWEB)

    Croitoru, Catalin [“Transilvania” University of Brasov, Materials Engineering and Welding Department, Eroilor 29 Str., 500036 Brasov (Romania); Patachia, Silvia, E-mail: st.patachia@unitbv.ro [“Transilvania” University of Brasov, Product Design Environment and Mechatronics Department, Eroilor 29 Str., 500036 Brasov (Romania); Papancea, Adina [“Transilvania” University of Brasov, Product Design Environment and Mechatronics Department, Eroilor 29 Str., 500036 Brasov (Romania); Baltes, Liana; Tierean, Mircea [“Transilvania” University of Brasov, Materials Engineering and Welding Department, Eroilor 29 Str., 500036 Brasov (Romania)

    2015-12-15

    Highlights: • Glass fibre-reinforced polyester composites surface analysis by photographic method. • The composites are submitted to accelerated ageing by UV irradiation at 254 nm. • The UV irradiation promotes differences in the surface chemistry of the composites. • MB dye is differently adsorbed on surfaces with different degradation degrees. • Good correlation between the colouring degree and surface chemistry. - Abstract: The paper presents a novel method for quantification of the modifications that occur on the surface of different types of gel-coated glass fibre-reinforced polyester composites under artificial UV-ageing at 254 nm. The method implies the adsorption of an ionic dye, namely methylene blue, on the UV-aged composite, and computing the CIELab colour space parameters from the photographic image of the coloured composite's surface. The method significantly enhances the colour differences between the irradiated composites and the reference, in contrast with the non-coloured ones. The colour modifications that occur represent a good indicative of the surface degradation, alteration of surface hydrophily and roughness of the composite and are in good correlation with the ATR-FTIR spectroscopy and optical microscopy results. The proposed method is easier, faster and cheaper than the traditional ones.

  13. The study on mechanism of holographic recording in photopolymer with dual monomer

    Science.gov (United States)

    Zhai, Qianli; Tao, Shiquan; Wang, Dayong

    2010-06-01

    In this paper we study the dynamics of refractive index modulation in a dual-monomer photopolymer through grating growth under different experiment stages. By using different sets of parameters for vinyl monomers (NVC) and acrylate monomers (POEA) respectively, a composite dual-monomer model, extended from the uniform post-exposure (UPE) model for single monomer photopolymer, is proposed and fitted with the experiment data very well. Further discussions indicate that the dominant contribution to the total index modulation is made by NVC monomers, and a brief explanation of the function of POEA monomers is given.

  14. PMR polyimide composites for aerospace applications. [Polymerization of Monomer Reactants

    Science.gov (United States)

    Serafini, T. T.

    1984-01-01

    A novel class of addition-type polyimides has been developed in response to the need for high temperature polymers with improved processability. The new plastic materials are known as PMR (for in situ polymerization of monomer reactants) polyimides. The highly processable PMR polyimides have made it possible to realize much of the potential of high temperature resistant polymers. Monomer reactant combinations for several PMR polyimides have been identified. The present investigation is concerned with a review of the current status of PMR polyimides. Attention is given to details of PMR polyimide chemistry, the processing of composites and their properties, and aerospace applications of PMR-15 polyimide composites.

  15. Cationically polymerizable monomers derived from renewable sources. Annual performance report

    Energy Technology Data Exchange (ETDEWEB)

    Crivello, J.V.

    1992-10-01

    The objectives of this project are to design and synthesize novel monomers which orginate from renewable biological sources and to carry out their rapid, efficient, pollution-free and energy efficient cationic polymerization to useful products under the influence of ultraviolet light or heat. A summary of the results of the past year`s research on cationically polymerizable monomers derived from renewable sources is presented. Three major areas of investigation corresponding to the different classes of naturally occurring starting materials were investigated; epoxidized terpenes and natural rubber and vinyl ethers from alcohols and carbohydrates.

  16. [Influence Factors on Monomer Conversion of Dental Composite Resin].

    Science.gov (United States)

    Wang, Shuang; Gao, Yan; Wang, Jing; Zhang, Yan; Zhang, Yuntao; Wang, Fanghui; Wang, Qingshan

    2015-04-01

    Dental composite resin is a kind of material which has been widely used in dental restoration. Research has found that the influence of residual monomer on the material mechanical, chemical and biological properties cannot be ignored. This paper elaborates these harms of residual monomers. The effects of resin matrix, inorganic filler and initiating system, illumination, secondarily treatment on the degree of conversion were also analyzed. The paper also discusses the effective measures to increase the conversion, and offers theoretical basis for the clinical application and development of composite resin.

  17. Breathing zone concentrations of methylmethacrylate monomer during joint replacement operations

    DEFF Research Database (Denmark)

    Darre, E; Jørgensen, L G; Vedel, P;

    1992-01-01

    By use of a methylmethacrylate (MMA) Dräger tube and bellow bump, the breathing zone concentrations of MMA monomer were measured for the operating surgeon during cementation of the components of hip and knee joint prostheses. The highest recordings (50-100 p.p.m.) were encountered during cementat......By use of a methylmethacrylate (MMA) Dräger tube and bellow bump, the breathing zone concentrations of MMA monomer were measured for the operating surgeon during cementation of the components of hip and knee joint prostheses. The highest recordings (50-100 p.p.m.) were encountered during...

  18. Functional finishing of aminated polyester using biopolymer-based polyelectrolyte microgels.

    Science.gov (United States)

    Glampedaki, Pelagia; Dutschk, Victoria; Jocic, Dragan; Warmoeskerken, Marijn M C G

    2011-10-01

    This study focuses on a microgel-based functionalization method applicable to polyester textiles for improving their hydrophilicity and/or moisture-management properties, eventually enhancing wear comfort. The method proposed aims at achieving pH-/temperature-controlled wettability of polyester within a physiological pH/temperature range. First, primary amine groups are created on polyester surfaces using ethylenediamine; second, biopolymer-based polyelectrolyte microgels are incorporated using the natural cross-linker genipin. The microgels consist of the pH-responsive natural polysaccharide chitosan and pH/thermoresponsive poly(N-isopropylacrylamide-co-acrylic acid) microparticles. Scanning electron microscopy confirmed the microgel presence on polyester surfaces. X-ray photoelectron spectroscopy revealed nitrogen concentration, supporting increased microscopy results. Electrokinetic analysis showed that functionalized polyester surfaces have a zero-charge point at pH 6.5, close to the microgel isoelectric point. Dynamic wetting measurements revealed that functionalized polyester has shorter total water absorption time than the reference. This absorption time is also pH dependent, based on dynamic contact angle and micro-roughness measurements, which indicated microgel swelling at different pH values. Furthermore, at 40 °C functionalized polyester has higher vapor transmission rates than the reference, even at high relative humidity. This was attributed to the microgel thermoresponsiveness, which was confirmed through the almost 50% decrease in microparticle size between 20 and 40 °C, as determined by dynamic light scattering measurements.

  19. The biomechanical evaluation of polyester as a tension band for the internal fixation of patellar fractures.

    LENUS (Irish Health Repository)

    McGreal, G

    2012-02-03

    We use a braided polyester suture in place of cerclage wire in tension band fixations. The objective of this study was to test the biomechanical properties of this technique. Sixteen cadaveric patellae were fractured and repaired by modified tension band fixation. Eight were fixed using eighteen gauge stainless steel wire as a tension band and eight using braided polyester. All specimens were subjected to tensile testing. Polyester was 75.0% as strong as wire. For dynamic testing, the patellae of seven cadaveric knees were fractured and then fixed with polyester tension bands. These were mounted in a device capable of extending the knees from 90 degrees to neutral against an applied force. None of the fixations failed. Three of the specimens fixed using 18 gauge stainless steel wire were compared with three fixed using polyester over 2000 cycles of knee flexion and extension. Polyester performed as well as wire. We conclude that polyester is an acceptable alternative to wire in tension band fixation.

  20. 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.

  1. Influence of pressure on the ferroelectric phase transition in a symmetrical polymerizable diacetylene crystal DNP

    Science.gov (United States)

    Even, J.; Bertault, M.; Girard, A.; Délugeard, Y.

    1996-12-01

    DNP is a symmetrical disubstituted polymerizable diacetylene RCCCCR where R is CH 2O(NO 2) 2. The monomer crystal of DNP undergoes a ferroelectric phase transition at low temperature; it disappears in fully polymerized DNP crystal because polymerization changes the diacetylene backbone conformation. We show that hydrostatic isotropic pressure also stabilizes the ferroelectric phase in the DNP monomer crystal by enhancing van der Waals interactions between side groups.

  2. Recent Advances in the Design of Water Based-Flame Retardant Coatings for Polyester and Polyester-Cotton Blends

    Directory of Open Access Journals (Sweden)

    Jenny Alongi

    2016-10-01

    Full Text Available Over the last ten years a new trend of research activities regarding the flame retardancy of polymeric materials has arisen. Indeed, the continuous search for new flame retardant systems able to replace the traditional approaches has encouraged alternative solutions, mainly centred on nanotechnology. In this context, the deposition of nanostructured coatings on fabrics appears to be the most appealing and performance suitable approach. To this aim, different strategies can be exploited: from the deposition of a single monolayer consisting of inorganic nanoparticles (single-step adsorption to the building-up of more complex architectures derived from layer by layer assembly (multi-step adsorption. The present paper aims to review the application of such systems in the field of polyester and polyester-cotton blend fabrics. The results collated by the authors are discussed and compared with those published in the literature on the basis of the different deposition methods adopted. A critical analysis of the advantages and disadvantages exhibited by these approaches is also presented.

  3. STUDY ON THE BLENDS OF NYLON 66 AND LIQUID CRYSTALLINE POLYESTERS

    Institute of Scientific and Technical Information of China (English)

    Zhang Shufan; Ren Jinghong

    1991-01-01

    Blends of polyamide (Nylon 66 ) with two different kinds of liquid crystalline polyesters were studied in all the composition range. Homogeneous samples were obtained by coprecipitation from 2wt%. solution of blends. The thermal properties, crystallinity and morphology of these blends were studied by using DSC, polarizing microscopy, and scanning electron microscopy. The phase transition and morphology of the blends are markedlyinfluenced by the composition of liquid crystalline polyesters. The mechanical behaviour of PHB/HNA-Nylon 66 blend was improved .although polyamide (Nylon 66)with the liquid crystalline polyesters were incompatible, but a rather strong interaction between the polymers did exist.

  4. Investigation of Mechanical Properties of Unidirectional Steel Fiber/Polyester Composites: Experiments and Micromechanical Predictions

    DEFF Research Database (Denmark)

    Raghavalu Thirumalai, Durai Prabhakaran; Løgstrup Andersen, Tom; Bech, Jakob Ilsted

    2016-01-01

    The article introduces steel fiber reinforced polymer composites, which is considered new for composite product developments. These composites consist of steel fibers or filaments of 0.21 mm diameter embedded in a polyester resin. The goal of this investigation is to characterize the mechanical...... performance of steel fiber reinforced polyester composites at room temperature. The mechanical properties of unidirectional steel fiber reinforced polyester composites (SFRP) are evaluated experimentally and compared with the predicted values by micro-mechanical models. These predictions help to understand...

  5. Effect of Blending Ratio on the Properties of Ramie/Polyester Blended Yarn

    Institute of Scientific and Technical Information of China (English)

    YU Wen

    2002-01-01

    The effects of the blending ratio on the properties of Ramie/Polyester blended yarns are discussed in this paper. The experimental results show that the elongation of the yarn with the polyester content more than 40% is better than that of others. There is a lowest tenacity of the yarn corresponding to the blending ratio of 50/50 or so. The other properties of the yarn, such as the evenness and hairiness, will be improved with the increasing of the polyester content.

  6. Study on the improvement of hydrophilic character on polyvinylalcohol treated polyester fabric

    Directory of Open Access Journals (Sweden)

    S. Pitchai

    2014-12-01

    Full Text Available Polyester fabric was treated with polyvinyl alcohol in alkaline medium. The moisture regain, water retention and wettability of the PVA treated polyester fabric were tested. The PVA treated PET fabric was dyed with disperse dye. The presence of PVA in the treated PET fabric was assessed by spot test. The treated fabric was also characterized by scanning electron microscope, FTIR and differential scanning calorimetry. The PVA treated polyester fabric showed improved hydrophilic character over intact and sodium hydroxide treated PET fabrics.

  7. One-bath Dyeing of Polyester/Wool Blend with Disperse Dyes

    Institute of Scientific and Technical Information of China (English)

    蔡翔; 宋心远

    2001-01-01

    The role of auxiliary LAB as vehicle in dyeing polyester/wool blends with disperse dyes is described. Dye exhaustion and bonding on polyester/wool samples are studied under different experimental conditions - the LAB amount, the temperature and pH value- to achieve optimum conditions. The results are compared with those obtained with and without conventional dyeing auxiliary products. Although dye exhaustion is higher in the presence of commercial carriers, the dye bonded increases markedly in the presence of auxiliary LAB in both fibers. The role played by auxiliary LAB in polyester/wool blend dyeing can provide a new method for this process.

  8. The antifungal activity of corona treated polyamide and polyester fabrics loaded with silver nanoparticles

    Science.gov (United States)

    Saponjic, Z.; Ilic, V.; Vodnik, V.; Mihailovic, D.; Jovancic, P.; Nedeljkovic, J.; Radetic, M.

    2008-07-01

    This study is aimed to highlight the possibility of using the corona treatment for fiber surface activation that can facilitate the loading of silver nanoparticles from colloids onto the polyester and polyamide fabrics and thus enhance their antifungal activity against Candida albicans. Additionally, the laundering durability of achieved effects was studied. Corona activated polyamide and polyester fabrics loaded with silver nanoparticles showed better antifungal properties compared to untreated fabrics. The positive effect of corona treatment became even more prominent after 5 washing cycles, especially for polyester fabrics.

  9. WH2 domain: a small, versatile adapter for actin monomers.

    Science.gov (United States)

    Paunola, Eija; Mattila, Pieta K; Lappalainen, Pekka

    2002-02-20

    The actin cytoskeleton plays a central role in many cell biological processes. The structure and dynamics of the actin cytoskeleton are regulated by numerous actin-binding proteins that usually contain one of the few known actin-binding motifs. WH2 domain (WASP homology domain-2) is a approximately 35 residue actin monomer-binding motif, that is found in many different regulators of the actin cytoskeleton, including the beta-thymosins, ciboulot, WASP (Wiskott Aldrich syndrome protein), verprolin/WIP (WASP-interacting protein), Srv2/CAP (adenylyl cyclase-associated protein) and several uncharacterized proteins. The most highly conserved residues in the WH2 domain are important in beta-thymosin's interactions with actin monomers, suggesting that all WH2 domains may interact with actin monomers through similar interfaces. Our sequence database searches did not reveal any WH2 domain-containing proteins in plants. However, we found three classes of these proteins: WASP, Srv2/CAP and verprolin/WIP in yeast and animals. This suggests that the WH2 domain is an ancient actin monomer-binding motif that existed before the divergence of fungal and animal lineages.

  10. Microstructure Control in the emulsion polymerization of fluorinated monomers

    Energy Technology Data Exchange (ETDEWEB)

    Apostolo, Marco [Ausimont R and D, Bollate (Italy); Morbidelli, Massimo [ETH Zentrum, Zuerich (Switzerland)

    1997-03-01

    In this paper a mathematical model able to evaluate the microstructure of fluorinated polymers is presented. The model uses the pseudo-homo polymerization approach to describe the kinetic evolution of polymerization reactions involving any number of monomer species. The molecular weight distribution is evaluated combining the classical leading moments method with a recently proposed model based on the numerical fractionation technique.

  11. Synthesis of a benzoxazine monomer containing maleimide and allyloxy groups

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A novel benzoxazine monomer 3-(4-allyloxy)phenyl-3,4-dihydro-2H-6-(N-maleimido)-1,3-benzoxazine (AMB) was synthesized and structure was confirmed by FT-IR, 1H NMR. Thermal analysis (DSC) of AMB showed the introduction of allyloxy group decreased melting point and exhibited a narrow and symmetric curing exothermic window.

  12. Influence of the Diene Monomer on Devulcanization of EPDM Rubber

    NARCIS (Netherlands)

    Verbruggen, M.A.L.; van der Does, L.; Noordermeer, Jacobus W.M.; van Duin, M.

    2008-01-01

    Ethylene–propylene–diene rubbers (EPDM) with 2-ethylidene-5-norbornene (ENB), dicyclopentadiene (DCPD), and 1,4-hexadiene (HD) as third monomers have been vulcanized with peroxide and with a conventional sulfur vulcanization recipe, and their devulcanization was subsequently investigated for

  13. Epoxy resin monomers with reduced skin sensitizing potency.

    Science.gov (United States)

    O'Boyle, Niamh M; Niklasson, Ida B; Tehrani-Bagha, Ali R; Delaine, Tamara; Holmberg, Krister; Luthman, Kristina; Karlberg, Ann-Therese

    2014-06-16

    Epoxy resin monomers (ERMs), especially diglycidyl ethers of bisphenol A and F (DGEBA and DGEBF), are extensively used as building blocks for thermosetting polymers. However, they are known to commonly cause skin allergy. This research describes a number of alternative ERMs, designed with the aim of reducing the skin sensitizing potency while maintaining the ability to form thermosetting polymers. The compounds were designed, synthesized, and assessed for sensitizing potency using the in vivo murine local lymph node assay (LLNA). All six epoxy resin monomers had decreased sensitizing potencies compared to those of DGEBA and DGEBF. With respect to the LLNA EC3 value, the best of the alternative monomers had a value approximately 2.5 times higher than those of DGEBA and DGEBF. The diepoxides were reacted with triethylenetetramine, and the polymers formed were tested for technical applicability using thermogravimetric analysis and differential scanning calorimetry. Four out of the six alternative ERMs gave polymers with a thermal stability comparable to that obtained with DGEBA and DGEBF. The use of improved epoxy resin monomers with less skin sensitizing effects is a direct way to tackle the problem of contact allergy to epoxy resin systems, particularly in occupational settings, resulting in a reduction in the incidence of allergic contact dermatitis.

  14. Aggregation processes with catalysis-driven monomer birth/death

    Institute of Scientific and Technical Information of China (English)

    Chen Yu; Han An-Jia; Ke Jian-Hong; Lin Zhen-Quan

    2006-01-01

    We propose two solvable cluster growth models, in which an irreversible aggregation spontaneously occurs between any two clusters of the same species; meanwhile, monomer birth or death of species A occurs with the help of species B. The system with the size-dependent monomer birth/death rate kernel K(i,j) = Jijv is then investigated by means of the mean-field rate equation. The results show that the kinetic scaling behaviour of species A depends crucially on the value of the index v. For the model with catalysis-driven monomer birth, the cluster-mass distribution of species A obeys the conventional scaling law in the v ≤ 0 case, while it satisfies a generalized scaling form in the v>0 case; moreover, the total mass of species A is a nonzero value in the v< 0 case while it grows continuously with time in the v>0 case. For the model with catalysis-driven monomer death, the cluster-mass distribution also approaches the conventional scaling form in the v < 0 case, while the conventional scaling description of the system breaks down in the v ≥ 0 case. Additionally, the total mass of species A retains a nonzero quantity in the v <0 case, but it decreases to zero with time in the v ≥ 0 case.

  15. Influence of the diene monomer on devulcanization of EPDM rubber

    NARCIS (Netherlands)

    Verbruggen, M.; Does, van der L.; Noordermeer, J.W.M.; Duin, van M.

    2008-01-01

    Ethylene–propylene–diene rubbers (EPDM) with 2-ethylidene-5-norbornene (ENB), dicyclopentadiene (DCPD), and 1,4-hexadiene (HD) as third monomers have been vulcanized with peroxide and with a conventional sulfur vulcanization recipe, and their devulcanization was subsequently investigated for recycli

  16. Binding interactions between suberin monomer components and pesticides

    Energy Technology Data Exchange (ETDEWEB)

    Olivella, M.À., E-mail: angels.olivella@udg.edu [Department of Chemical Engineering, Escola Politècnica Superior, Universitat de Girona, Maria Aurèlia Capmany, 61, 17071 Girona (Spain); Bazzicalupi, C.; Bianchi, A. [Department of Chemistry “Ugo Schiff”, University of Florence, Via della Lastruccia, 3, 50019 Sesto Fiorentino (Italy); Río, J.C. del [Instituto de Recursos Naturales y Agrobiología de Sevilla, Consejo Superior de Investigaciones Científicas, P.O. Box 1052, 41080 Seville (Spain); Fiol, N.; Villaescusa, I. [Department of Chemical Engineering, Escola Politècnica Superior, Universitat de Girona, Maria Aurèlia Capmany, 61, 17071 Girona (Spain)

    2015-09-15

    Understanding the role of biomacromolecules and their interactions with pollutants is a key for elucidating the sorption mechanisms and making an accurate assessment of the environmental fate of pollutants. The knowledge of the sorption properties of the different constituents of these biomacromolecules may furnish a significant contribution to this purpose. Suberin is a very abundant biopolymer in higher plants. In this study, suberin monomers isolated from cork were analyzed by thermally-assisted methylation with tetramethylammonium hydroxide (TMAH) in a pyrolysis unit coupled to gas chromatography–mass spectrometry (GC/MS). The isolated monomer mixture was used to study the sorption of three pesticides (isoproturon, methomyl and oxamyl). The modes of pesticide–sorbent interactions were analyzed by means of two modeling calculations, the first one representing only the mixture of suberin monomers used in the sorption study, and the second one including glycerol to the mixture of suberin monomers, as a building block of the suberin molecule. The results indicated that the highest sorption capacity exhibited by the sorbent was for isoproturon (33%) being methomyl and oxamyl sorbed by the main suberin components to a lesser extent (3% and < 1%, respectively). In addition to van der Waals interactions with the apolar region of sorbent and isoproturon, modeling calculations evidenced the formation of a hydrogen bond between the isoproturon NH group and a carboxylic oxygen atom of a suberin monomer. In the case of methomyl and oxamyl only weak van der Waals interactions stabilize the pesticide–sorbent adducts. The presence of glycerol in the model provoked significant changes in the interactions with isoproturon and methomyl. - Highlights: • Suberin has low affinity to retain pesticides of aliphatic character. • Suberin has a moderate affinity to adsorb isoproturon. • Modeling calculations show that apolar portion of suberin interacts with isoproturon.

  17. [Modification of the composite resin with the hyperbranched polyester and evaluation of the mechanical properties of the modified composite resin].

    Science.gov (United States)

    Luo, Y C; Sun, S; Xiao, Y H

    2016-04-09

    To study the effect of hyperbranched polyester(HBP)on mechanical properties of the conventional resin matrix. Two hyperbranched monomers(HBP2-X and HBP2-Y)were synthesized and incorporated at 40%(by mass)into a 2∶1(by mass)bisphenol-A diglycidyl methacrylate(Bis-GMA): triethylene glycol dimethacrylate(TEGDMA)resin. Bis-GMA/TEGDMA without the incorporation of hyperbranched polyester was used as control(n=8 per group). The mechanical properties of the modified neat resin, including polymerization volumetric shrinkage, Vickers hardness, water absorption and dissolution rate, as well as the flexural strength, compressive strength and diametral tensile strength of the composite resin with different content of filler(0%, 30%, 50%, 70%)were measured. Mechanical properties of the composite resin were measured by universal testing machine. The results were analyzed by the ANOVA and LSD-t-test. The resin with HBP greatly decreased the polymerization shrinkage of the composite resin, and the value of group X was(6.32±0.49)%, and that of group Y was(6.31±0.68)%, whereas that of the control group was(8.14 ± 0.53)%. The value of volumetric shrinkage of the modified groups were significantly lower than that of the control group(Presin(Pcomposite materials, with 70% inorganic filler, there were no significant difference in the value of flexural strength among the groups(P>0.05). There was no significant difference in the value of compressive strength, between group X([244 ± 13]MPa)and the standard group([234 ± 17]MPa)(P>0.05). However, they were significantly higher than that in group Y([204 ± 24]MPa)(P0.05), but both were significantly lower than that in group X([41.1 ± 3.0]MPa)(Presin that was modified with the HBP, we should make further analysis and study based on the property of low volumetric shrinkage, to strive for the development of low volumetric shrinkage of HBP, without affecting its mechanical properties.

  18. Morphological and biodegradability studies of Euphorbia latex modified polyester - Banana fiber composites

    Science.gov (United States)

    Rai, Bhuvneshwar; Kumar, Gulshan; Diwan, R. K.

    2016-05-01

    The composites of Banana fiber were prepared using polyester resin blended Euphorbia coagulum, morphology and the degree of rate of aerobic biodegradation of the prepared composites were studied. Polyester resin blended Euphorbia coagulum containing Banana fiber, Euphorbia coagulum and polyester resin taken in the ratio 40: 24: 36 was used for the study, which was the optimum composition of the composite reported in a previous study by the authors. In the biodegradability study cellulose has been used as positive reference material. Result shows that Euphorbia coagulum modified polyester - Banana fiber composites exhibited biodegradation to the extent of around 40%. The use of developed green composites may help in reducing the generation of non-biodegradable polymeric wastes.

  19. Azobenzene Polyesters Used as Gate‐Like Scaffolds in Nanoscopic Hybrid Systems

    DEFF Research Database (Denmark)

    Bernardos, Andrea; Mondragón, Laura; Javakhishvili, Irakli

    2012-01-01

    The synthesis and characterisation of new capped silica mesoporous nanoparticles for on‐command delivery applications is reported. Functional capped hybrid systems consist of MCM‐41 nanoparticles functionalised on the external surface with polyesters bearing azobenzene derivatives and rhodamine B...

  20. Plasma treatment of polyester fabric to impart the water repellency property

    Indian Academy of Sciences (India)

    C J Jahagirdar; L B Tiwari

    2007-04-01

    Polyester fabric is treated with DCDMS solution by two methods: dipping the fabric directly in DCDMS solution for different intervals and dipping the fabric in DCDMS solution after its exposure into RF plasma chamber for different durations at optimized exposure power conditions. The physical properties of polyester fabric treated with DCDMS in the presence or absence of air plasma have been compared with control fabric. Different characterization techniques like scanning electron microscope, attenuated total reflectance-IR and Dataflash 100 colour measurement spectrophotometer are used to assess the surface morphology, composition and change in colour parameters. Water repellency property of both untreated and modified polyester fabric is studied using AATCC test method 39 (1971). The effectiveness of the water repellency property of modified polyester fabric is checked by repeated washing up to ten cycles.

  1. Research of Kinetics of Electroless Ni-Cu-P Alloy Plating on Polyester Fabric

    Institute of Scientific and Technical Information of China (English)

    CHEN Zhen-bing; CHEN Xiao-li

    2002-01-01

    All the variables that may affect the Ni- Cu-P alloy deposition rate on polyester fabric were studied, and the activation energy and the reaction orders were determined. The deposition rate equation was also derived.

  2. Effect of polyester fiber reinforcement on the mechanical properties of interim fixed partial dentures

    Directory of Open Access Journals (Sweden)

    N. Gopichander

    2015-10-01

    Conclusion: Within the limitations of this study, polyester fiber reinforcements improved the mechanical properties of heat-polymerized PMMA, cold-polymerized PMMA, and bis-acrylic provisional FPD materials.

  3. Dyeing of UV irradiated cotton and polyester fabrics with multifunctional reactive and disperse dyes

    Directory of Open Access Journals (Sweden)

    Ijaz Ahmad Bhatti

    2016-03-01

    Full Text Available The dyeing behaviour of UV irradiated cotton and polyester fabrics using multifunctional reactive and disperse dyes has been investigated. The plain, woven, mercerized, bleached, cotton and polyester fabrics were exposed to UV radiation (180 w, 254 nm for 30, 60, 90 and 120 min. Dyeing was performed using irradiated fabric with a dye solution of un-irradiated reactive and disperse/azo dyes. The dyeing parameters such as, temperature, time, pH and salt concentration have been optimized. The colour strength values of dyed fabrics were evaluated by comparing irradiated and un-irradiated cotton and polyester fabrics in CIE Lab systems using spectra flash SF600. Finally ISO standard methods were employed to observe the effect of UV radiation on fastness properties. It was found that UV radiation has a potential to improve the colour strength values of cotton and polyester fabrics by using reactive and disperse dyes.

  4. Catalytic water dissociation using hyperbranched aliphatic polyester (Boltorn series) as the interface of a bipolar membrane.

    Science.gov (United States)

    Xue, Yanhong; Xu, Tongwen; Fu, Rongqiang; Cheng, Yiyun; Yang, Weihua

    2007-12-15

    The effect of hyperbranched aliphatic polyester (Boltorn series) on the water dissociation in bipolar membranes was firstly investigated in this paper. The bipolar membranes were prepared by immersing the anion exchange layer in a hyperbranched aliphatic polyester solution and then coating on the layer a polyphenylene oxide (SPPO) solution. The SEM observations proved the existence of hyperbranched aliphatic polyester at the membrane intermediate layer. The adsorption amount was evaluated by the oxygen content via XPS. The junction thickness of the prepared bipolar membrane was determined by electrochemical impedance spectroscopy (EIS), and the membrane performances were evaluated by current-voltage curves. The results showed that the amount and generation of Boltorn series, and temperature all affected I-V behaviors of the fabricated bipolar membranes, and the former two played the critical role. These effects were explained on the basis of the water dissociation theory and the characteristics of hyperbranched aliphatic polyester.

  5. Eco-friendly surface modification on polyester fabrics by esterase treatment

    Science.gov (United States)

    Wu, Jindan; Cai, Guoqiang; Liu, Jinqiang; Ge, Huayun; Wang, Jiping

    2014-03-01

    Currently, traditional alkali deweighting technology is widely used to improve the hydrophilicity of polyester fabrics. However, the wastewater and heavy chemicals in the effluent cause enormous damage to the environment. Esterase treatment, which is feasible in mild conditions with high selectivity, can provide a clean and efficient way for polyester modification. Under the optimum conditions, the polyester fabric hydrolysis process of esterase had a linear kinetics. X-ray photoelectron spectrometry (XPS) results showed that hydroxyl and carboxyl groups were produced only on the surface of modified fiber without changing the chemical composition of the bulk. These fibers exhibited much improved fabric wicking, as well as greatly improved oily stain removal performance. Compared to the harsh alkali hydrolysis, the enzyme treatment led to smaller weight loss and better fiber integrity. The esterase treatment technology is promising to produce higher-quality polyester textiles with an environmental friendly approach.

  6. Study of the indoor decontamination using nanocoated woven polyester fabric

    Science.gov (United States)

    Memon, Hafeezullah; Kumari, Naveeta; Jatoi, Abdul Wahab; Khoso, Nazakat Ali

    2016-11-01

    This research primarily deals with the photocatalytic degradation of methanol in indoor air using nanocoated indoor textiles used for curtains as household textiles. The woven polyester was coated by titanium dioxide by sol gel method, using silicon-based binder. The characterization of the coating has been done using scanning electron microscopy (SEM) image analysis, energy dispersive analysis using X-ray (EDAX) and Fourier transform infrared spectroscopy (FTIR). The DIY instrument providing the similar environment as of indoor was designed to assess the performance of the degradation of formaldehyde under UV light. The photocatalytic degradation rate was measured using the absorption value of the solutions obtained in the result of liquid chromatography of test solution and reagent solution. Different amount of dosages (1-3 %) and different time period of coatings (half hour to 3 h) have been evaluated for optimization.

  7. Tensile properties of bacterial cellulose nanofibers - polyester composites

    Science.gov (United States)

    Abral, H.; Mahardika, M.

    2016-07-01

    The paper shows tensile properties of bacterial cellulose (BC) nanofibers and polyester (PO) matrix composites. Tensile properties including tensile strength (TS), modulus elasticity (ME), and elongation (EL) were observed respectively. BC nanofibers exist in the form of a sheet that was then varied in matrix PO. The BC sheet was mounted by one, three, five and seven pieces respectively in the matrix PO. The tensile strength of the composites was conducted by using the tensile equipment. The results showed that the tensile strength of the composite with a single sheet of BC was lower than that of pure PO. The ST value achieved maximum level in the number of layers of BC three pieces, but then it decreased for the composites reinforced five and seven pieces of BC nanofiber, respectively. Scanning Electron Microscope (SEM) observation exhibits bad interface bonding between BC nanofibers and PO matrix.

  8. The research of far infrared flame retardant polyester staple fiber

    Science.gov (United States)

    Li, Qingshan; Zhang, Kaijun; Luo, Jinqong; Li, Ji’an; Jiang, Jian; Liang, Qianqian; Jin, Yongxia; Liu, Bing

    2017-01-01

    Far infrared flame retardant slices was prepared, fiber with far infrared flame retardant composite function was also prepared by the method of melt spinning. Scanning electron microscopy (SEM) was used to observe the fibrous microscopic structure. In the SEM images, functional ultrafine powder particle size and distribution in the fiber were visible. The results show that the functional ultrafine powder is evenly distributed on the fibrous surface, which is closely combined with fiber, and the far infrared emissivity is F, which is more than (8 to 14 microns) 0.88. Far infrared flame retardant polyester fiber has not only good flame retardant, but also environmental health effect: releasing negative ions and launch far-infrared, which shows wide application prospect. The fiber was processed into far-infrared flame retardant electric blanket, whose functional indicators and flame retardant properties are not reduced.

  9. Polyester Sulphonic Acid Interstitial Nanocomposite Platform for Peroxide Biosensor

    Directory of Open Access Journals (Sweden)

    Emmanuel I. Iwuoha

    2009-12-01

    Full Text Available A novel enzyme immobilization platform was prepared on a platinum disk working electrode by polymerizing aniline inside the interstitial pores of polyester sulphonic acid sodium salt (PESA. Scanning electron microscopy study showed the formation of homogeneous sulphonated polyaniline (PANI nanotubes (~90 nm and thermogravimetric analysis (TGA confirmed that the nanotubes were stable up to 230 °C. The PANI:PESA nanocomposite showed a quasi-reversible redox behaviour in phosphate buffer saline. Horseradish peroxidase (HRP was immobilized on to this modified electrode for hydrogen peroxide detection. The biosensor gave a sensitivity of 1.33 μA (μM-1 and a detection limit of 0.185 μM for H2O2. Stability experiments showed that the biosensor retained more than 64% of its initial sensitivity over four days of storage at 4 °C.

  10. Glass fibres reinforced polyester composites degradation monitoring by surface analysis

    Science.gov (United States)

    Croitoru, Catalin; Patachia, Silvia; Papancea, Adina; Baltes, Liana; Tierean, Mircea

    2015-12-01

    The paper presents a novel method for quantification of the modifications that occur on the surface of different types of gel-coated glass fibre-reinforced polyester composites under artificial UV-ageing at 254 nm. The method implies the adsorption of an ionic dye, namely methylene blue, on the UV-aged composite, and computing the CIELab colour space parameters from the photographic image of the coloured composite's surface. The method significantly enhances the colour differences between the irradiated composites and the reference, in contrast with the non-coloured ones. The colour modifications that occur represent a good indicative of the surface degradation, alteration of surface hydrophily and roughness of the composite and are in good correlation with the ATR-FTIR spectroscopy and optical microscopy results. The proposed method is easier, faster and cheaper than the traditional ones.

  11. Application of polyester derived from biomass in petroleum asphalt cement

    Directory of Open Access Journals (Sweden)

    Fernando de Araújo

    Full Text Available Abstract This study evaluated the effects of the incorporation of a new additive to asphalt cement oil (CAP. A polyol product was obtained through the oxypropylation reaction of sugarcane bagasse. This polyol was polymerised with pyromellitic anhydride in order to obtain a polyester (BCP to test its suitability in terms of the material properties to be applied as additives. FTIR spectra of the polymerised material (BCP confirmed the occurrence of chemical modification due to the appearance of a new band at 1750 cm-1, characteristic of ester groups. The TGA data showed that the BCP product had higher thermal stability than the polyol. According to the softening point and elastic recovery tests, the incorporation of 11% and 16% w/w BCP in conventional CAP met the specifications of regulatory standards.

  12. Simulation of Continuous Esterification Process of Polyester Polyols

    Institute of Scientific and Technical Information of China (English)

    CHEN Like; XI Zhenhao; QIN Zhen; ZHAO Ling; YUAN Weikang

    2013-01-01

    Based on the kinetic and thermodynamic equations,a comprehensive mathematical model for the continuous esterification process of polyester polyols was developed,which was carried out in an innovational bubbling reactive distillation tower (BRDT) at atmospheric pressure.In this new type of reactor,direct esterification between ethylene glycol and adipic acid was accomplished efficiently and rapidly.A bench BRDT with the height of 2 m was applied for the esterification process of poly (ethylene adipate) (PEA).In the continuous operation,linear oligomers were discharged from the bottom of the column,while water passed a few column trays and a packing section as a condensation byproduct.The influence of major operating conditions on reactor performance was also simulated.Simulation results were in good agreement with experimental data,providing a strategy for developing and optimizing this process.

  13. Polypropylene Fibers as Reinforcements of Polyester-Based Composites

    Directory of Open Access Journals (Sweden)

    Gonzalo Martínez-Barrera

    2013-01-01

    Full Text Available Effects of gamma radiation and the polypropylene fibers on compressive properties of polymer concrete composites (PC were studied. The PCs had a composition of 30 wt% of unsaturated polyester resin and 70 wt% of marble particles which have three different sizes (small, medium, and large. The PCs were submitted to 200, 250, and 300 kGy of radiation doses. The results show that the compressive properties depend on the combination of the polypropylene fiber concentration and the applied radiation dose. The compressive strength value is highest when using medium particle size, 0.1 vol% of polypropylene fibers and 250 kGy of dose; moreover, the compressive modulus decreases when increasing the particle size.

  14. Synthesis of functionalized CNTs/hyperbranched polyester nanocomposites

    Science.gov (United States)

    Pan, Yufeng; Cui, Xiaokun; Zhang, Yue

    2017-01-01

    Carbon nanotubes (CNTs) were unzipped using the modified Hummer method to prepare the CNTs-GO microstructure (see Fig. 1). A new type of CNTs-GO-H20 nanocomposite has been synthesized by grafting hyperbranched (HB) polyester (Boltorn H20) brushes on the CNTs-GO by coupling agent (KH560). The morphology of CNTs-GO-H20 was characterized by FTIR, TEM, XPS and TGA. The FT-IR data and XPS data evidenced that CNTs-GO-H20 nanocomposites were synthesized successfully. The addition of CNTs improved the thermal stability of the nanocomposites. The TEM data showed that the CNTs-GO microstructure was also prepared. These electrochemical measurements results indicated that coatings provided greater protection against corrosion behavior. Moreover, the nanocomposite material improved corrosion resistance of the coating.

  15. Effect of Charge and Hydrophobicity on Adsorption of Modified Starches on Polyester.

    Science.gov (United States)

    Samu; Moulee; Kumar

    1999-12-15

    Polyester fabric (poly(ethylene terephthalate)) is a hydrophobic polymer. Its hydrophobic nature can be a disadvantage for certain applications like dyeing, finishing, detergency, etc. Physical or chemical modification of the polyester to make it more hydrophilic is therefore desirable for certain performance characteristics. Surface modification of polyester to make it hydrophilic can be achieved by adsorbing polymers on the polyester surface. Starch is a commonly available, hydrophilic polymer used in many textile applications that can be used to modify polyester. However, it needs to be chemically modified so that it can adsorb on the polyester fabric and physically modify the fabric characteristics. The polymers used in this study are two different modified starches-cationic and anionic starches and mixtures of the two. The adsorption kinetics on a polyester substrate was studied. The effect of charge and hydrophobicity on adsorption was investigated. Cationic starches were shown to readily adsorb on polyester and this was attributed to electrostatic interactions. Hydrophobic substituents on the cationic moiety resulted in increased adsorption. This was attributed to the weak hydrophobic interaction between the polymer chains which could result in a more coiled polymer conformation. It is hypothesized that more starch molecules are required for surface coverage of the polyester, resulting in an increase in adsorption. Anionic starch was adsorbed on the substrate but at a slower rate than the cationic starches. It is likely that there is a H bonding between acid groups on the starch and the ester groups of the polyester. However, the anionic starch is desorbed when the polyester is placed in an aqueous medium. When a blend of cationic starch and anionic starch was used, a low concentration of anionic starch was seen to increase adsorption, indicating that the polyelectrolyte complex itself may be adsorbing on the substrate. Further increases cause a decrease in

  16. Polyester-based thin films with high photosensitivity

    Energy Technology Data Exchange (ETDEWEB)

    POTTER,KELLY SIMMONS; POTTER JR.,BARRETT G.; WHEELER,DAVID R.; JAMISON,GREGORY M.

    2000-02-29

    A great deal of research has been done to understand the photosensitive optical response of inorganic glasses, which exhibit a permanent, photo-induced refractive index change due to the presence of optically active point defects in the glass structure. In the present work, the authors have performed a preliminary study of the intrinsic photosensitivity of a polyester containing a cinnamylindene malonate group (CPE, a photo- and thermal-crosslinkable group) for use in photonic waveguide devices. Thin films of CPE (approximately 0.5 microns thick) were spun onto fused silica substrates. Optical absorption in the thin films was evaluated both before and after exposure to UV radiation sources. It was found that the polyester exhibits two dominant UV absorption bands centered about 240 nm and 330 nm. Under exposure to 337 nm radiation (nitrogen laser) a marked bleaching of the 330 nm band was observed. This band bleaching is a direct result of the photo-induced crosslinking in the cinnamylindene malonate group. Exposure to 248 nm radiation (excimer laser), conversely, resulted in similar bleaching of the 330 nm band but was accompanied by nearly complete bleaching of the higher energy 240 nm band. Based on a Kramers-Kronig analysis of the absorption changes, refractive index changes on the order of {minus}10{sup {minus}2} are estimated. Confirmation of this calculation has been provided via ellipsometry which estimates a refractive index change at 632 nm of {minus}0.061 {+-} 0.002. Thus, the results of this investigation confirm the photosensitive potential of this type of material.

  17. Polyester-based (bio)degradable polymers as environmentally friendly materials for sustainable development.

    Science.gov (United States)

    Rydz, Joanna; Sikorska, Wanda; Kyulavska, Mariya; Christova, Darinka

    2014-12-29

    This review focuses on the polyesters such as polylactide and polyhydroxyalkonoates, as well as polyamides produced from renewable resources, which are currently among the most promising (bio)degradable polymers. Synthetic pathways, favourable properties and utilisation (most important applications) of these attractive polymer families are outlined. Environmental impact and in particular (bio)degradation of aliphatic polyesters, polyamides and related copolymer structures are described in view of the potential applications in various fields.

  18. The identification of cutin synthase: formation of the plant polyester cutin

    DEFF Research Database (Denmark)

    Yeats, Trevor H.; Martin, Laetitia B. B.; Viart, Helene Marie-France;

    2012-01-01

    A hydrophobic cuticle consisting of waxes and the polyester cutin covers the aerial epidermis of all land plants, providing essential protection from desiccation and other stresses. We have determined the enzymatic basis of cutin polymerization through characterization of a tomato extracellular...... acyltransferase, CD1, and its substrate, 2-mono(10,16-dihydroxyhexadecanoyl)glycerol. CD1 has in vitro polyester synthesis activity and is required for cutin accumulation in vivo, indicating that it is a cutin synthase....

  19. The identification of cutin synthase: formation of the plant polyester cutin.

    Science.gov (United States)

    Yeats, Trevor H; Martin, Laetitia B B; Viart, Hélène M-F; Isaacson, Tal; He, Yonghua; Zhao, Lingxia; Matas, Antonio J; Buda, Gregory J; Domozych, David S; Clausen, Mads H; Rose, Jocelyn K C

    2012-07-01

    A hydrophobic cuticle consisting of waxes and the polyester cutin covers the aerial epidermis of all land plants, providing essential protection from desiccation and other stresses. We have determined the enzymatic basis of cutin polymerization through characterization of a tomato extracellular acyltransferase, CD1, and its substrate, 2-mono(10,16-dihydroxyhexadecanoyl)glycerol. CD1 has in vitro polyester synthesis activity and is required for cutin accumulation in vivo, indicating that it is a cutin synthase.

  20. The identification of cutin synthase: formation of the plant polyester cutin

    OpenAIRE

    Yeats, Trevor H.; Martin, Laetitia B. B.; Viart, Hélène M.-F.; Isaacson, Tal; He, Yonghua; Zhao, Lingxia; Matas, Antonio J.; Buda, Gregory J.; Domozych, David S.; Clausen, Mads H.; Rose, Jocelyn K. C.

    2012-01-01

    A hydrophobic cuticle consisting of waxes and the polyester cutin covers the aerial epidermis of all land plants, providing essential protection from desiccation and other stresses. We have determined the enzymatic basis of cutin polymerization through characterization of a tomato extracellular acyltransferase, CD1, and its substrate, 2-mono(10,16-dihydroxyhexadecanoyl)glycerol (2-MHG). CD1 has in vitro polyester synthesis activity and is required for cutin accumulation in vivo, indicating th...

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

    DEFF Research Database (Denmark)

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

    1999-01-01

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

  2. Optimizing the Dyeing Process of Alkali-Treated Polyester Fabric with Dolu Natural Dye

    OpenAIRE

    M. F. Shahin; Ahmed, R. M.

    2014-01-01

    An attempt has been made to optimize the process of dyeing polyester (PET) fabric with natural dyes. Polyester has been first treated with NaOH solution in order to study its impact on the dyeability to the natural dye. The required and used colour component was extracted from a natural plant, namely: Rhubarb; Rheum officinale. The chemical structure of the used colouring matter is observed to have all the characteristics of a typical disperse dye. The colour strength of PE...

  3. Polyester-Based (Biodegradable Polymers as Environmentally Friendly Materials for Sustainable Development

    Directory of Open Access Journals (Sweden)

    Joanna Rydz

    2014-12-01

    Full Text Available This review focuses on the polyesters such as polylactide and polyhydroxyalkonoates, as well as polyamides produced from renewable resources, which are currently among the most promising (biodegradable polymers. Synthetic pathways, favourable properties and utilisation (most important applications of these attractive polymer families are outlined. Environmental impact and in particular (biodegradation of aliphatic polyesters, polyamides and related copolymer structures are described in view of the potential applications in various fields.

  4. Near-ultraviolet tyrosyl circular dichroism of pig insulin monomers, dimers, and hexamers. Dipole-dipole coupling calculations in the monopole approximation.

    Science.gov (United States)

    Strickland, E H; Mercola, D

    1976-08-24

    The tyrosyl circular dichroism (CD) has been calculated using the conformation of pig insulin observed in rhombohedral crystals containing 2 zinc atoms per hexamer. These calculations predict that the tyrosyl CD at 275 nm will be enhanced disproportionally as monomers interact to form dimers and as dimers interact to form hexamers. This enhanced tyrosyl CD (delta epsilon per 5800 molecular weight) results from new coupling interactions generated in the regions of contact between monomers and between dimers. These calculations illustrate that a large CD enhancement may accompany aggregation even in the absence of a conformation change in eith monomer. The tyrosyl CD intensities calculated for monomers, dimers, and hexamers of 2-zinc pig insulin are compatible with the experimentally observed CD spectra which are enhanced about fourfold in the hexamer compared with the monomer. Zinc ions and other metals do not contribute directly to the tyrosyl CD but only influence the optical properties by promoting the hexameric state. The relation of the integrity of the molecule to dimer formation and the biological activity of the molecules are discussed. The largest calculated contributions to tryosyl CD arise from interactions with far-ultraviolet transitions of neighboring aromatic groups. In the hexamer, about half of the tyrosyl CD intensity is calculated to arise from Tyr-A14.

  5. STUDIES ON THE PERMEABILITY OF PVC /EBBA OVERLAPPED ULTRATHIN COMPOSITE MEMBRANES MODIFIED BY PLASMA- POLYMERIZATION WITH FLUOROCARBON MONOMERS

    Institute of Scientific and Technical Information of China (English)

    FU Xiucheng; JIN Xigao; Tisato KAJIYAMA

    1989-01-01

    The PVC/EBBA ultrathin composite membranes with thickness of about 100 nm were prepared by spreading the solution on water surface. The overlapped composite membrane showed a characteristic aggregation structure in which the polymer matrix exists as a three-dimensional spongy network and the liquid crystal domains were observedThe surface modification for the overlapped membranes was carried out by means of plasma-polymerization with the monomers of fluorocarbon compounds. Both Arrhenius plots of permeability coefficients for oxygen (-Po2) in the membrane samples before and after modification showed significant increase in the vicinity of the TKN of EBBA.

  6. Polymer as a function of monomer: Analytical quantum modeling

    CERN Document Server

    Nakhaee, Mohammad

    2016-01-01

    To identify an analytical relation between the properties of polymers and their's monomer a Metal-Molecule-Metal (MMM) junction has been presented as an interesting and widely used object of research in which the molecule is a polymer which is able to conduct charge. The method used in this study is based on the Green's function approach in the tight-binding approximation using basic properties of matrices. For a polymer base MMM system, transmission, density of states (DOS) and local density of states (LDOS) have been calculated as a function of the hamiltonian of the monomer. After that, we have obtained a frequency for LDOS variations in pass from a subunit to the next one which is a function of energy.

  7. Formaldehyde stabilization facilitates lignin monomer production during biomass depolymerization.

    Science.gov (United States)

    Shuai, Li; Amiri, Masoud Talebi; Questell-Santiago, Ydna M; Héroguel, Florent; Li, Yanding; Kim, Hoon; Meilan, Richard; Chapple, Clint; Ralph, John; Luterbacher, Jeremy S

    2016-10-21

    Practical, high-yield lignin depolymerization methods could greatly increase biorefinery productivity and profitability. However, development of these methods is limited by the presence of interunit carbon-carbon bonds within native lignin, and further by formation of such linkages during lignin extraction. We report that adding formaldehyde during biomass pretreatment produces a soluble lignin fraction that can be converted to guaiacyl and syringyl monomers at near theoretical yields during subsequent hydrogenolysis (47 mole % of Klason lignin for beech and 78 mole % for a high-syringyl transgenic poplar). These yields were three to seven times those obtained without formaldehyde, which prevented lignin condensation by forming 1,3-dioxane structures with lignin side-chain hydroxyl groups. By depolymerizing cellulose, hemicelluloses, and lignin separately, monomer yields were between 76 and 90 mole % for these three major biomass fractions. Copyright © 2016, American Association for the Advancement of Science.

  8. Dynamics of Aggregate Growth Through Monomer Birth and Death

    Institute of Scientific and Technical Information of China (English)

    KE Jian-Hong; LIN Zhen-Quan

    2004-01-01

    @@ We investigate the kinetic behaviour of the growth of aggregates through monomer birth and death and propose a simple model with the rate kernels K(k) ∝ ku and K′(k) ∝ kv at which the aggregate Ak of size k respectively yields and loses a monomer. For the symmetrical system with K(k) = K′(k), the aggregate size distribution approaches the conventional scaling form in the case of u < 2, while the system may undergo a gelation-like transition in the u > 2 case. Moreover, the typical aggregate size S(t) grows as t1/(2-u) in the u < 2 case and increases exponentially with time in the u = 2 case. We also investigate several solvable systems with asymmetrical rate kernels and find that the scaling of the aggregate size distribution may break down in most cases.

  9. Dielectric Response and Broadband Microwave Absorption Properties of Three-Layer Graded ZnO Nanowhisker/Polyester Composites

    Institute of Scientific and Technical Information of China (English)

    ZHOU Yan; SHI Xiao-Ling; YUAN Jie; FANG Xiao-Yong; CAO Mao-Sheng

    2007-01-01

    We design and prepare three-layer graded ZnO nanowhisker/polyester composites. The dispersion configuration of ZnO nanowhiskers in the polyester is investigated, and their microwave reflectivity curves are also measured. Experimental results have shown that the graded dispersion with ZnO nanowhiskers contributes to broadband microwave absorption. In other words, the absorption band depends on the graded dispersion configuration of ZnO nanowhiskers in polyester matrix.

  10. Effect of fiber loading on the mechanical and physical properties of “green” bagasse–polyester composite

    OpenAIRE

    2015-01-01

    The main aim of this work is to fill unsaturated polyester resin with bagasse agricultural waste, as reinforcement, to prepare green wooden–polymer composites. Bagasse fibers were treated with 5% sodium hydroxide and then with dilute sulfuric acid. Bagasse–polyester composites were prepared by addition of 5, 10 and 15% of untreated and alkali treated bagasse fibers to polyester. The crosslinking reaction was performed using methyl ethyl ketone peroxide as a catalyst and cobalt octoate as an a...

  11. Novel fluoro-carbon functional monomer for dental bonding.

    Science.gov (United States)

    Yoshihara, K; Yoshida, Y; Hayakawa, S; Nagaoka, N; Kamenoue, S; Okihara, T; Ogawa, T; Nakamura, M; Osaka, A; Van Meerbeek, B

    2014-02-01

    Among several functional monomers, 10-methacryloxydecyl dihydrogen phosphate (10-MDP) bonded most effectively to hydroxyapatite (HAp). However, more hydrolysis-resistant functional monomers are needed to improve bond durability. Here, we investigated the adhesive potential of the novel fluoro-carbon functional monomer 6-methacryloxy-2,2,3,3,4,4,5,5-octafluorohexyl dihydrogen phosphate (MF8P; Kuraray Noritake Dental Inc., Tokyo, Japan) by studying its molecular interaction with powder HAp using solid-state nuclear magnetic resonance ((1)H MAS NMR) and with dentin using x-ray diffraction (XRD) and by characterizing its interface ultrastructure at dentin using transmission electron microscopy (TEM). We further determined the dissolution rate of the MF8P_Ca salt, the hydrophobicity of MF8P, and the bond strength of an experimental MF8P-based adhesive to dentin. NMR confirmed chemical adsorption of MF8P onto HAp. XRD and TEM revealed MF8P_Ca salt formation and nano-layering at dentin. The MF8P_Ca salt was as stable as that of 10-MDP; MF8P was as hydrophobic as 10-MDP; a significantly higher bond strength was recorded for MF8P than for 10-MDP. In conclusion, MF8P chemically bonded to HAp. Despite its shorter size, MF8P possesses characteristics similar to those of 10-MDP, most likely to be associated with the strong chemical bond between fluorine and carbon. Since favorable bond strength to dentin was recorded, MF8P can be considered a good candidate functional monomer for bonding.

  12. Syntheses of New Functionalized Monomers for π-Conjugated Polymers

    Institute of Scientific and Technical Information of China (English)

    D.VYPRACHTICKY; V.CIMRO; P.PAVLKOVA; I.KMNEK

    2007-01-01

    1 Results Tailored monomers based on the activated esters of 2,5-dibromobenzoic (sulfonic) acid derivatives, the 3-substituted 2,5-dibromothiophenes, the 9-substituted 2,7-dibromocarbazoles, and on the brominated 1,10-phenanthrolines suitable for Suzuki, Yamamoto or Grignard metathesis (GRIM) coupling reactions were synthesized and characterized by melting point, elemental analysis, 1H NMR, FTIR and TLC. The Horner-Wadsworth-Emmons reaction mechanism was utilized for the preparation of the 3-[2-(pyren-1...

  13. Development of high performance vinyl acetate monomer (VAM) catalysts

    OpenAIRE

    2009-01-01

    The focus of this study was to develop high performance catalysts for the synthesis of vinyl acetate monomer (VAM). By systematic variation of different preparation parameters a multitude of shell catalysts consisting of PdAu nanoparticles supported on a bentonite carrier was explored. In order to investigate the influence of these alterations on catalytic performance, a catalyst classification was accomplished in a high-throughput Temkin test unit by comparison with a highly efficient commer...

  14. Synthesis of a new aromatic dianhydride monomer and related polyimide

    Institute of Scientific and Technical Information of China (English)

    Yun Xia Wei; Ming Guang Ma; Guo Hu Zhao; Sheng Ying Li; Ming Kai Chen

    2009-01-01

    A novel aromatic dianhydride monomer,3,3'-oxybis[(3,4-dicarboxyphenoxy)phenol]dianhydride,was successfully synthe-sized in three steps using 3,3'-oxybis(phenol)as starting material,which was reacted with 4,4'-oxydianiline(ODA)via a conventional thermal or chemical imidization method to produce a new polyimide.The resulting polyimide exhibited excellent solubility,and film-forming capability.

  15. Polymerization in Liquid Crystal Medium: Preparation of Polythiophene Derivatives Bearing a Bulky Pyrimidine Substituent

    Directory of Open Access Journals (Sweden)

    Hiromasa Goto

    2010-10-01

    Full Text Available We carried out polycondensation of monomers bearing a bulky pyrimidine substituent in a liquid crystal solvent. The resultant polymers formed nematic liquid crystals. The polymers prepared in liquid crystals had higher coplanarity than the polymers prepared in toluene. This can be due to the fact that the ordered medium of the liquid crystal produces an aggregated structure with well-developed π-stacking between the main chains. The present results demonstrated that polymerization of bulky monomers is possible in liquid crystal solvents.

  16. Ortho-substituted triptycene-based diamines, monomers, and polymers, methods of making and uses thereof

    KAUST Repository

    Ghanem, Bader Saleh

    2017-04-13

    Described herein are ortho-dimethyl-substituted and tetramethyi-substituted triptycene-containing diamine monomers and microporous triptycene-based poiyimides and poiyamides, and methods of making the monomers and polymers.

  17. Thermally stable drilling fluid additive comprised of a copolymer of catechol-based monomer

    Energy Technology Data Exchange (ETDEWEB)

    Patel, A.D.

    1986-06-17

    A water soluble polymer is described having thermal stability and exhibiting utility as an aqueous drilling fluid additive comprising: (a) a major portion of a catechol based monomer; (b) a minor portion of a dicarboxylic acid monomer.

  18. 脂肪族超支化聚酯的合成与性能研究%STUDY ON SYNTHESIS AND PROPERTIES OF HYPERBRANCHED ALIPHATIC POLYESTER

    Institute of Scientific and Technical Information of China (English)

    肖文清; 程万里; 胡剑青; 涂伟萍

    2008-01-01

    The different generation hyperbranched aliphatic polyesters were synthesized based upon 2,2-Bis(methylol)propionic acid as a AB2 monomer, and Neopentyl glycol as a core molecule through one step polymerization process. The structure and properties of the product were characterized by FTIR, 1H NMR, GPC and TGA. It was shown that the third generation hyperbranched polyester has narrow molecular weight distribution with Mw=2 615 g/mol, Mn=1 536 g/mol, PDI=1.41 by GPC. The degree of branching, as determined by quantitative 1H NMR spectroscopy, was found to be 0.49. TGA analysis showed that the polymer exhibited high thermal stability, the decomposition temperature is more than 300 ℃. The conversion of carboxyl groups of the third generation hyperbranched polyeste was discussed. Because the water which is produced in this reaction could't be emitted totally, as a result, the final carboxyl groups conversation rate still could't get to 100% .%以新戊二醇为核,2,2-二羟甲基丙酸为支化单体,通过准一步熔融缩聚法合成了不同代数的脂肪族超支化聚酯.采用FT-IR、1H NMR、GPC及TGA方法对所合成的超支化聚酯的结构与性能进行了表征和分析.对第三代超支化聚酯而言,GPC分析测得重均分子量为2 615 g/mol,质均分子量为1 536 g/mol,分子量分布为1.41;1H NMR分析测得其支化度为0.49,热重分析表明温度高达300 ℃该聚酯才失重5wt%.此外还讨论了第三代脂肪族超支化聚酯熔融缩聚过程羧基的变化,结果表明,由于反应生成的水不能完全除去,羧基的最终转化率不可能达到100%.

  19. SYNTHESIS AND CHARACTERIZATION OF A NOVEL STYRYLTHIOPHENE MONOMER AND CORRESPONDING POLYURETHANE FOR NLO MATERIALS

    Institute of Scientific and Technical Information of China (English)

    Jiang-hong Wang; Jian-feng Zhai; Jia-yun Zhou; Yu-xia Zhao; Yu-quan Shen

    1999-01-01

    A novel monomer,(trans)-7-[4-N,N-(di-β-hydroxyethyl) amino-benzene]-ethenyl-3,5-dinitro-thiophene (HBDT), was synthesized and characterized. The details of synthesizing the monomer and prepolymer, polyurethane with the monomer covalently incorporated are presented. The prepolymer and polyurethane exhibited good solubility in common organic solvents. Molecular nonlinear optical properties of the monomer (HBDT) substituted thiophene based stilbenes is presented.

  20. Electromagnetic wave control of ceramic/resin photonic crystals with diamond structure

    Directory of Open Access Journals (Sweden)

    Soshu Kirihara, Mitsuo Takeda, Kazuaki Sakoda and Yoshinari Miyamoto

    2004-01-01

    Full Text Available Millimeter-order photonic crystals with the periodic arrangement of the dielectric constant were fabricated by infiltrating the mixed slurry of ceramics and polyester into the epoxy molds with an inverse form of a diamond structure. The epoxy molds are designed and processed by using a CAD/CAM process of stereolithography. The photonic crystals were prepared to have the diamond structure of the ceramic/polyester composite lattice, which is embedded in the epoxy matrix. The ceramic powders mixed with polyester are TiO2, SrTiO3, and BaTiO3 with high dielectric constant. It is possible to control more freely and widely the dielectric constant of the photonic crystals by this method. These ceramic/resin photonic crystals formed the complete photonic band gaps in the microwave band of 7–11 GHz, which can totally reflect the electromagnetic wave for all crystal directions. Attenuation profiles of the transmission amplitude in the band gaps were controlled with the dielectric constant of the composite lattice. The obtained results fairly agreed with the theoretical simulation of the electromagnetic wave propagation through photonic crystals.

  1. Frustrated polymer crystal structures

    Science.gov (United States)

    Lotz, B.; Strasbourg, 67083

    1997-03-01

    Several crystal structures or polymorphs of chiral or achiral polymers and biopolymers with three fold conformation of the helix have been found to conform to a common and -with one exception(Puterman, M. et al, J. Pol. Sci., Pol. Phys. Ed., 15, 805 (1977))- hitherto unsuspected packing scheme. The trigonal unit-cell contains three isochiral helices; the azimuthal setting of one helix differs significantly from that of the other two, leading to a so-called frustrated packing scheme, in which the environment of conformationally identical helices differs. Two variants of the frustrated scheme are analyzed. Similarities with frustrated two dimensional magnetic systems are underlined. Various examples of frustration in polymer crystallography are illustrated via the elucidation or reinterpretation of crystal phases or polymorphs of polyolefins, polyesters, cellulose derivatives and polypeptides. Structural manifestations (including AFM evidence) and morphological consequences of frustration are presented, which help diagnose the existence of this original packing of polymers.(Work done with L. Cartier, D. Dorset, S. Kopp, T. Okihara, M. Schumacher, W. Stocker.)

  2. 稀土元素化合物在聚酯聚合工艺中的催化作用%The Catalytic Property of Rare-Earth Element Compound on Polyester Polymerisation Process

    Institute of Scientific and Technical Information of China (English)

    蒋志勇

    2012-01-01

    Rare-earth compound and rare-earth/Sb2O3 complex catalysts for polyester transesterification and polycondensation by DMT route were studied. Also the properties of polyesters and process parameters were analyzed. The results showed that rare-earth compound was used as catalysts for polyester transesterification and associate catalysts for polyester polycondensation. Rare-earth compound/Sb2O3 complex catalyst could enhance the reaction efficiency, reduce the reaction time and lower initial temperature of transesterification. At the same time, the L value and crystallization capabilities of polyester by rare-earth com-pound/Sb2O3 complex catalyst was higher than stibium compound catalysts. Efficiency of polyester catalyzed by heavy organic rare-earth compound-was better than light inorganic rare-earth compound.%以不同的稀土金属元素化合物及稀土化合物/三氧化二锑复合物分别用作聚酯酯交换和缩聚催化剂,对各工艺参数进行分析,并对产品性能进行测试与表征.结果表明:稀土化合物可作为聚酯酯交换的催化剂和缩聚助催化剂;使用稀土化合物/三氧化二锑复合催化剂,能有效提高酯交换效率,缩短反应时间,降低酯交换开始温度,所得聚酯产品的色相优于普通三氧化二锑催化所得聚酯,结晶度比普通三氧化二锑催化所得聚酯的高,且重稀土有机化合物比轻稀土无机化合物催化效率更高.

  3. Bioengineering of bacteria to assemble custom-made polyester affinity resins.

    Science.gov (United States)

    Hay, Iain D; Du, Jinping; Burr, Natalie; Rehm, Bernd H A

    2015-01-01

    Proof of concept for the in vivo bacterial production of a polyester resin displaying various customizable affinity protein binding domains is provided. This was achieved by engineering various protein binding domains into a bacterial polyester-synthesizing enzyme. Affinity binding domains based on various structural folds and derived from molecular libraries were used to demonstrate the potential of this technique. Designed ankyrin repeat proteins (DARPins), engineered OB-fold domains (OBodies), and VHH domains from camelid antibodies (nanobodies) were employed. The respective resins were produced in a single bacterial fermentation step, and a simple purification protocol was developed. Purified resins were suitable for most lab-scale affinity chromatography purposes. All of the affinity domains tested produced polyester beads with specific affinity for the target protein. The binding capacity of these affinity resins ranged from 90 to 600 nmol of protein per wet gram of polyester affinity resin, enabling purification of a recombinant protein target from a complex bacterial cell lysate up to a purity level of 96% in one step. The polyester resin was efficiently produced by conventional lab-scale shake flask fermentation, resulting in bacteria accumulating up to 55% of their cellular dry weight as polyester. A further proof of concept demonstrating the practicality of this technique was obtained through the intracellular coproduction of a specific affinity resin and its target. This enables in vivo binding and purification of the coproduced "target protein." Overall, this study provides evidence for the use of molecular engineering of polyester synthases toward the microbial production of specific bioseparation resins implementing previously selected binding domains.

  4. Poly(ester amide)s from Poly(ethylene terephthalate) Waste for Enhancing Bone Regeneration and Controlled Release.

    Science.gov (United States)

    Natarajan, Janeni; Madras, Giridhar; Chatterjee, Kaushik

    2017-08-30

    The present study elucidates the facile synthesis and exceptional properties of a family of novel poly(ester amide)s (PEAs) based on bis(2-hydroxy ethylene) terephthalamide that was obtained from the poly(ethylene terephthalate) waste. Fourier transform infrared and (1)H NMR were used to verify the presence of ester and amide in the polymer backbone. Differential scanning calorimetry data showed that the glass transition temperature decreased with as the chain length of dicarboxylic acids increased. Dynamic mechanical analysis and contact angle studies proved that the modulus values and hydrophobicity increased with as the chain lengths of dicarboxylic acids increased. In vitro hydrolytic degradation and dye release studies demonstrated that the degradation and release decreased with as the chain lengths of dicarboxylic acids increased. Modeling these data illustrated that degradation and release follow first-order degradation and zero-order release, respectively. The in vitro cytocompatibility studies confirmed the minimal toxicity characteristic of these polymers. Osteogenic studies proved that these polymers can be highly influential in diverting the cells toward osteogenic lineage. Alizarin red staining evinced the presence of twice the amount of calcium phosphate deposits by the cells on these polymers when compared to the control. The observed result was also corroborated by the increased expression of alkaline phosphatase. These findings were further validated by the markedly higher mRNA expressions for known osteogenic markers using real time polymerase chain reaction. Therefore, these polymers efficiently promoted osteogenesis. This study demonstrates that the physical properties, degradation, and release kinetics can be altered to meet the specific requirements in organ regeneration as well as facilitate simultaneous polymer resorption through control of the chain length of the monomers. The findings of this study have significant implications for

  5. A High-hydrophobic Polyester Prepared by Polymerization-Dissolution-Precipitation Method%用聚合-溶解-析出法制备强疏水性聚酯

    Institute of Scientific and Technical Information of China (English)

    金剑; 王雪; 肖长发

    2011-01-01

    Hydrophobically-modified polyester (MPET) was synthesized by employing poly(ethylene terephthalate) (PET) as the major components of molecular chain and hydroxy-fluorosilicone polymer (FGX) as the third monomer, was characterized by 1H-NMR and ESCA, and the influence of dissolutionprecipitation factors on the surface morphology, hydrophobicity and tensile strength were investigated. It was found that the likeness of the surface particles and the hydrophobicity of the samples were connected with the dissolving time. The high-hydrophobic polyester prepared by dissolution-precipitation method has the similar micro- and nanostructured surface to loft surface.%以聚对苯二甲酸乙二酯(PET)为分子链主要成分,引入第三单体聚羟基氟硅油(FGX),共聚出疏水改性共聚酯(MPET).用1H-NMR、ESCA对MPET进行表征,研究了溶解-析出条件对MPET材料表面形貌、疏水性能及力学性能的影响.结果表明,样品表面结晶析出粒子的形状和疏水效果与溶解时间相关.用溶解-析出法制备的强疏水聚酯具有与荷叶相类似的微纳米阶层结构.

  6. Liquid crystals in tribology.

    Science.gov (United States)

    Carrión, Francisco-José; Martínez-Nicolás, Ginés; Iglesias, Patricia; Sanes, José; Bermúdez, María-Dolores

    2009-09-18

    Two decades ago, the literature dealing with the possible applications of low molar mass liquid crystals, also called monomer liquid crystals (MLCs), only included about 50 references. Today, thousands of papers, conference reports, books or book chapters and patents refer to the study and applications of MLCs as lubricants and lubricant additives and efforts are made to develop new commercial applications. The development of more efficient lubricants is of paramount technological and economic relevance as it is estimated that half the energy consumption is dissipated as friction. MLCs have shown their ability to form ordered boundary layers with good load-carrying capacity and to lower the friction coefficients, wear rates and contact temperature of sliding surfaces, thus contributing to increase the components service life and to save energy. This review includes the use of MLCs in lubrication, and dispersions of MLCs in conventional polymers (PDMLCs). Finally, new lubricating system composed of MLC blends with surfactants, ionic liquids or nanophases are considered.

  7. Recycling polyester from waste polyester-cotton blends%利用废弃涤棉混纺纤维回收涤纶

    Institute of Scientific and Technical Information of China (English)

    孔伟; 于永玲; 吕丽华

    2012-01-01

    The separation process of waste polyester-cotton fiber blends with dilute acid was studied to recycle polyester. The effect of hydrochloric acid concentration, reaction time, reaction temperature and solid-liquid ratio on the separation and recovery of polyester was studied through orthogonal experiment. The results showed that the impact factors order were: reaction time > mass fraction > reaction temperature > ratio of solid to liquid. The optimal conditions were: 10% of hydrochloric acid concentration, 40 g/L of liquid, 95 ℃ and 90 min. The polyester fibers were hydrolyzed into fibrous and cotton fiber were hydrolyzed into small powders after reaction so that the polyester was got.%对稀酸法分离废弃涤棉混纺纤维,回收涤纶的工艺过程进行了研究.采用正交试验考察了盐酸质量分数、反应时间、反应温度及固液比等因素对分离回收涤纶效果的影响.研究表明,影响因素的显著性大小依次为:反应时间、盐酸质量分数、反应温度、固液比.最优工艺为:盐酸质量分数10%,固液比40 g/L,温度95℃,反应时间90 min.反应后的涤纶成纤维状,棉纤维水解成细小粉末,通过过滤分离达到了回收涤纶的目的.

  8. Optimizing the delamination failure in bamboo fiber reinforced polyester composite

    Directory of Open Access Journals (Sweden)

    N. Abilash

    2016-01-01

    Full Text Available Delamination is represented to be the most prevalent failure in composite structures. The use of composites in the manufacturing sector plays a very important role in the industry in general. Moreover these materials have unique characteristics when analyzed separately from constituents which are a part of them. In this paper, a partially ecological composite was made, using natural fibers as reinforcement (bamboo fiber, in the polyester resin matrix to form a composite, seeking to improve the mechanical behavior among its class of materials. The characteristics of a composite material are determined by how it behaves while machining, Drilling is the most predominant machining process because of its cost effectiveness when compared with other processes. Obviously delamination is the major problem that is focused by many researchers while selecting drilling as the machining process in polymeric composites. This research mainly emphasizes on the critical parameters by varying its speed, feed, and diameter of the cutting tool, their contribution to delamination was analyzed. Reduced delaminations were identified by varying the speed and feed rate.

  9. Fungal communities associated with degradation of polyester polyurethane in soil.

    Science.gov (United States)

    Cosgrove, Lee; McGeechan, Paula L; Robson, Geoff D; Handley, Pauline S

    2007-09-01

    Soil fungal communities involved in the biodegradation of polyester polyurethane (PU) were investigated. PU coupons were buried in two sandy loam soils with different levels of organic carbon: one was acidic (pH 5.5), and the other was more neutral (pH 6.7). After 5 months of burial, the fungal communities on the surface of the PU were compared with the native soil communities using culture-based and molecular techniques. Putative PU-degrading fungi were common in both soils, as soil, and only a few species in the PU communities were detectable in the soil, indicating that only a small subset of the soil fungal communities colonized the PU. Soil type influenced the composition of the PU fungal communities. Geomyces pannorum and a Phoma sp. were the dominant species recovered by culturing from the PU buried in the acidic and neutral soils, respectively. Both fungi degraded Impranil and represented >80% of cultivable colonies from each plastic. However, PU was highly susceptible to degradation in both soils, losing up to 95% of its tensile strength. Therefore, different fungi are associated with PU degradation in different soils but the physical process is independent of soil type.

  10. Identification and comparison of cutinases for synthetic polyester degradation.

    Science.gov (United States)

    Baker, Peter James; Poultney, Christopher; Liu, Zhiqiang; Gross, Richard; Montclare, Jin Kim

    2012-01-01

    Cutinases have been exploited for a broad range of reactions, from hydrolysis of soluble and insoluble esters to polymer synthesis. To further expand the biotechnological applications of cutinases for synthetic polyester degradation, we perform a comparative activity and stability analysis of five cutinases from Alternaria brassicicola (AbC), Aspergillus fumigatus (AfC), Aspergillus oryzae (AoC), Humicola insolens (HiC), and the well-characterized Fusarium solani (FsC). Of the cutinases, HiC demonstrated enhanced poly(ε-caprolactone) hydrolysis at high temperatures and under all pH values, followed by AoC and AfC. Both AbC and FsC are least stable and function poorly at high temperatures as well as at acidic pH conditions. Surface charge calculations and phylogenetic analysis reveal two important modes of cutinase stabilization: (1) an overall neutral surface charge within the "crowning area" by the active site and (2) additional disulfide bond formation. These studies provide insights useful for reengineering such enzymes with improved function and stability for a wide range of biotransformations.

  11. Enthalpy-Entropy Compensation in Polyester Degradation Reactions

    Directory of Open Access Journals (Sweden)

    Adam Al-Mulla

    2012-01-01

    Full Text Available In an earlier work the author had studied the degradation kinetics of polyethylene terephthalate (PET, polytrimethylene terephthalate (PTT, and polybutylene terephthalate (PBT under nonisothermal conditions in air and N2 at heating rates of 5, 10, 15, and 20°C/min. In this paper the kinetic degradation parameters of PET, PTT, and PBT were estimated using the Coats-Redfern method for two different weight loss regions ranging from 2–8% (Zone I and 8–40% (Zone II. A comparative analysis of the enthalpy-entropy compensation effect for these polyesters in air and N2 is presented. A linear relationship was found to exist between entropy and enthalpy values. The following criteria were applied to establish an enthalpy-entropy compensation effect and to check the presence of an isokinetic temperature: (a Exner’s plot of log k3T1 versus log k3T2, and (b Krug et al. linear regression of ΔH versus ΔG. By the use of the latter two methods, varying isokinetic temperatures were obtained. These temperatures were not in the range of the experimental work conducted, indicating that these systems do not display compensation phenomena.

  12. Development of Glass/Jute Fibers Reinforced Polyester Composite

    Directory of Open Access Journals (Sweden)

    Amit Bindal

    2013-01-01

    Full Text Available Composites play significant role as engineering material and their use has been increasing day by day due to their specific properties such as high strength to weight ratios, high modulus to weight ratio, corrosion resistance, and wear resistance. In present work, an attempt is made to hybridize the material using synthetic (glass as well as natural fibres (chemically treated jute, such that to reduce the overall use of synthetic reinforcement, to reduce the overall cost, and to enhance the mechanical properties. All composite specimens with different weight percentages of fibres were manufactured using hand lay-up process and testing was done by using ASTM standards. Experimental results revealed that hybridization of composite with natural and synthetic fibres shows enhanced tensile strength, flexural strength, and impact strength. The content of natural reinforcement was found to be in the range of 25–33.3% for best results. The effect of treated jute on flexural properties was more than that on tensile properties, which was due to greater stiffness of jute fibers. Chemical treatment of jute fibers lowers the water absorption and results were comparable to glass fiber reinforced polyester composites. The addition of jute also reduced the overall cost by 22.18%.

  13. Raman spectroscopy of thin-film silicon on woven polyester

    Energy Technology Data Exchange (ETDEWEB)

    Lind, Helena; Wilson, John [Department of Physics, School of Engineering and Physical Sciences, Heriot-Watt University, Riccarton, Edinburgh EH14 4AS (United Kingdom); Mather, Robert [Power Textiles Limited, Upland House, Ettrick Road, Selkirk TD7 5AJ (United Kingdom)

    2011-12-15

    Thin-film silicon deposited by plasma-enhanced chemical vapour deposition (PECVD), encompasses both hydrogenated amorphous silicon (a-Si:H) and 'nanocrystalline silicon' (nc-Si), the latter being a two-phase mixture of discrete nanocrystallites in an amorphous matrix. It is distinguished from a-Si:H by a characteristic Raman spectrum. As the film structure moves from amorphous to more crystalline, the Raman TO phonon spectral region no longer consists of a broad amorphous peak at {proportional_to}480 cm{sup -1} but instead has an obvious narrower peak located at higher wavenumber. The accepted signature peak for nc-Si lies between these two and most probably arises from the hexagonal, wurtzite structure of the nanocrystals. Here we use Raman spectroscopy to show how the structure of thin-film silicon on woven polyester is influenced by the substrate as well as by the deposition conditions. We find that the rough surface of the textile substrate enables nc-Si formation, provided that the correct deposition conditions are employed and that the substrate temperature does not exceed 210 C. Although the gas mixture is the dominant parameter for determining the film structure, and input power also has a significant effect, we find that a specific combination of these interrelated parameters is essential to control the final structure. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  14. Adsorption of proteins from plasma at polyester non-wovens.

    Science.gov (United States)

    Klomp, A J; Engbers, G H; Mol, J; Terlingen, J G; Feijen, J

    1999-07-01

    Polyester non-wovens in filters for the removal of leukocytes from platelet concentrates (PCs) must be platelet compatible. In PC filtration, the adsorption of proteins at the plasma-non-woven interface can be of great importance with respect to the yield of platelets. Unmodified and radio frequency glow discharge (RFGD) treated poly(ethylene terephthalate) non-woven (NW-PET) and two commercial surface-modified non-wovens were contacted with human plasma. Protein desorption by sodium dodecyl sulphate (SDS) was evaluated by X-ray photoelectron spectroscopy (XPS). The desorbed proteins were characterized by gel electrophoresis and immunoblotting. Compared to the commercial surface-modified non-wovens, unmodified and RFGD-treated NW-PETs adsorbed a relatively high amount of protein. Significantly more protein was removed from the hydrophobic NW-PET by SDS than from the hydrophilic RFGD-treated non-wovens. RFGD treatment of NW-PET reduces the reversibility of protein adsorption. Less albumin and fibrinogen were removed from the RFGD-treated non-wovens than from NW-PET. In addition, a large amount of histidine-rich glycoprotein was removed from RFGD-treated non-wovens, but not from NW-PET. The different behaviour of RFGFD-treated non-wovens towards protein adsorption is probably caused by differences in the chemical reactivity of the non-woven surfaces.

  15. Viscoelastic properties of kenaf reinforced unsaturated polyester composites

    Science.gov (United States)

    Osman, Ekhlas A.; Mutasher, Saad A.

    2014-03-01

    In order to quantify the effect of temperature on the mechanical and dynamic properties of kenaf fiber unsaturated polyester composites, formulations containing 10 wt.% to 40 wt.% kenaf fiber were produced and tested at two representative temperatures of 30°C and 50°C. Dynamic mechanical analysis was performed, to obtain the strain and creep compliance for kenaf composites at various styrene concentrations. It is possible to obtain creep curves at different temperature levels which can be shifted along the time axis to generate a single curve known as a master curve. This technique is known as the time-temperature superposition principle. Shift factors conformed to a William-Landel-Ferry (WLF) equation. However, more long term creep data was needed in order to further validate the applicability of time-temperature superposition principle (TTSP) to this material. The primary creep strain model was fitted to 60 min creep data. The resulting equation was then extrapolated to 5.5 days; the creep strain model of power-law was successfully used to predict the long-term creep behavior of natural fiber/thermoset composites.

  16. Semipermeable membranes based on specified tetrabromobisphenol type polyesters

    Energy Technology Data Exchange (ETDEWEB)

    Kawakami, J.H.; Muruganandam, N.; Brode, G.L.

    1991-10-08

    This patent describes a process for separating a component from an O{sub 2}/N or CO{sub 2}/CH{sub 4} gas mixture containing. It comprises: contracting the gas mixture with one side of a gas separation membrane comprising a thin layer predominantly of a polyester or copolyester derived form the reaction of an aromatic dicarboxylic acid or derivative thereof and greater than 50 mol percent of a tetrabromobisphenol, or divalent cyclododecyl and wherein the aromatic discarboxylic acid or divalent cyclododecyl and wherein the aromatic dicarboxylic acid or derivative thereof comprises 80 mole percent or more of isophthalic acid or its dichloride and/or 4-bromoisophthalic acid or its dichloride and 20 mole percent or less of terephthalic acid or its dichlorid and/or 2-bromoterephthalic acid or its dichloride as the dicarboxylic acid compound, or 30 mole percent or less of isophthaloyl dichloride and/or 4-homoisophthalic acid or its dichloride and 70 mole percent or more of terephthalic acid or its dichloride and/or 2-bromoterepohthalic acid or is dichloride; the membrane having a combination of high selectivity and high permeation rate values, while maintaining a pressure differential across the two sides of the membrane and removing the permeated component from the other side of the membrane.

  17. Disposable polyester-toner electrophoresis microchips for DNA analysis.

    Science.gov (United States)

    Duarte, Gabriela R M; Coltro, Wendell K T; Borba, Juliane C; Price, Carol W; Landers, James P; Carrilho, Emanuel

    2012-06-07

    Microchip electrophoresis has become a powerful tool for DNA separation, offering all of the advantages typically associated with miniaturized techniques: high speed, high resolution, ease of automation, and great versatility for both routine and research applications. Various substrate materials have been used to produce microchips for DNA separations, including conventional (glass, silicon, and quartz) and alternative (polymers) platforms. In this study, we perform DNA separation in a simple and low-cost polyester-toner (PeT)-based electrophoresis microchip. PeT devices were fabricated by a direct-printing process using a 600 dpi-resolution laser printer. DNA separations were performed on PeT chip with channels filled with polymer solutions (0.5% m/v hydroxyethylcellulose or hydroxypropylcellulose) at electric fields ranging from 100 to 300 V cm(-1). Separation of DNA fragments between 100 and 1000 bp, with good correlation of the size of DNA fragments and mobility, was achieved in this system. Although the mobility increased with increasing electric field, separations showed the same profile regardless of the electric field. The system provided good separation efficiency (215,000 plates per m for the 500 bp fragment) and the separation was completed in 4 min for 1000 bp fragment ladder. The cost of a given chip is approximately $0.15 and it takes less than 10 minutes to prepare a single device.

  18. [Migration of monomers and primary aromatic amines from nylon products].

    Science.gov (United States)

    Mutsuga, Motoh; Yamaguchi, Miku; Ohno, Hiroyuki; Kawamura, Yoko

    2010-01-01

    Migration of 2 kinds of monomer and 21 kinds of primary aromatic amines (PAAs) from 21 kinds of nylon products such as turners, ladles and wrap film were determined. Samples were classified as regards materials by mean of pyrolysis-GC/MS. One sample was classified as nylon 6, 15 samples as nylon 66 and three samples as nylon 6/66 copolymers, while two samples were laminate of nylon 6 with polyethylene or polypropylene. All of the nylon 66 samples contained a small amount of ε-caprolactam (CPL), which is the nylon 6 monomer. Migration levels of monomers and PAAs at 60°C for 30 min into 20% ethanol were measured by LC/MS/MS. CPL was detected at the level of 0.015-38 µg/mL from all samples, excluding one wrap film sample, and 1,6-hexamethylenediamine was detected at the level of 0.002-0.013 µg/mL from all nylon 66 samples and one nylon 6/66 sample. In addition, 0.006-4.3 µg/mL of 4,4'-diaminodiphenylmethane from three samples, 0.032-0.23 µg/mL of aniline from four samples, 0.001 µg/mL of 4-chloroaniline from two samples, and 0.002 µg/mL of 2-toluidine and 0.066 mg/mL of 1-naphthylamine from one sample each were detected. The migration levels at 95 or 121°C were about 3 and 10 times the 60°C levels, respectively.

  19. Evaluating the effects of crystallinity in new biocompatible polyester nanocarriers on drug release behavior.

    Science.gov (United States)

    Karavelidis, Vassilios; Karavas, Evangelos; Giliopoulos, Dimitrios; Papadimitriou, Sofia; Bikiaris, Dimitrios

    2011-01-01

    Four new polyesters based on 1,3-propanediol and different aliphatic dicarboxylic acids were used to prepare ropinirole HCl-loaded nanoparticles. The novelty of this study lies in the use of polyesters with similar melting points but different degrees of crystallinity, varying from 29.8% to 67.5%, as drug nanocarriers. Based on their toxicity to human umbilical vein endothelial cells, these aliphatic polyesters were found to have cytotoxicity similar to that of polylactic acid and so may be considered as prominent drug nanocarriers. Drug encapsulation in polyesters was performed via an emulsification/solvent evaporation method. The mean particle size of drug-loaded nanoparticles was 164-228 nm, and the drug loading content was 16%-23%. Wide angle X-ray diffraction patterns showed that ropinirole HCl existed in an amorphous state within the nanoparticle polymer matrices. Drug release diagrams revealed a burst effect for ropinirole HCl in the first 6 hours, probably due to release of drug located on the nanoparticle surface, followed by slower release. The degree of crystallinity of the host polymer matrix seemed to be an important parameter, because higher drug release rates were observed in polyesters with a low degree of crystallinity.

  20. An experimental study of shock wave propagation through a polyester film

    Science.gov (United States)

    Eliasson, Veronica; Jeon, Hongjoo

    2016-11-01

    A polyester film is available in a variety of uses such as packaging, protective overlay, barrier protection, and other industrial applications. In the current study, shock tube experiments are performed to study the influence of a polyester film on the propagation of a planar shock wave. A conventional shock tube is used to create incident shock Mach numbers of Ms = 1.34 and 1.46. A test section of the shock tube is designed to hold a 0.009 mm, 0.127 mm, 0.254 mm, or 0.508 mm thick polyester film (Dura-Lar). High-temporal resolution schlieren photography is used to visualize the shock wave mitigation caused by the polyester film. In addition, four pressure transducers are used to measure the elapsed time of arrival and overpressure of the shock wave both upstream and downstream of the test section. Results show that the transmitted shock wave in the polyester film is clearly observed and the transmitted shock Mach number is decreased by increasing film thickness. This study is supported by the National Science Foundation under Grant No. CBET-1437412.

  1. Thermo-Responsive Injectable MPEG-Polyester Diblock Copolymers for Sustained Drug Release

    Directory of Open Access Journals (Sweden)

    Hoon Hyun

    2014-10-01

    Full Text Available Thermo-responsive diblock copolymers composed of hydrophilic methoxy poly(ethylene glycol (MPEG and hydrophobic biodegradable polyesters were prepared for application as injectable drug delivery systems, because they show a thermo-responsive sol-to-gel transition, especially around body temperature, when dispersed in aqueous solutions. The thermogelling hydrogels formed by hydrophobic aggregation could be varied by changing the components of the hydrophobic polyester part. For the polyester block in the present study, 95 mol% of ε-caprolactone (CL was used for the main polyester chain and 5 mol% of p-dioxanone (DO was copolymerized randomly by the MPEG initiator in the presence of HCl as the catalyst. By adding a small portion of DO into the poly ε-caprolactone (PCL chains, the temperature range of gelation, the intensity of viscosity and the drug release behavior were changed. The MPEG-b-poly(ε-caprolactone-ran-p-dioxanone (MPEG-b-PCDO hydrogel showed the enhanced drug release in vitro and in vivo compared to MPEG-b-PCL hydrogel. Therefore, MPEG-polyester hydrogels may serve as minimally invasive and therapeutic, injectable hydrogel systems with adjustable temperature-responsive and biodegradable windows, as well as sustained release of drugs over a certain time period.

  2. Mechanical performance of hybrid polyester composites reinforced Cloisite 30B and kenaf fibre

    Science.gov (United States)

    Bonnia, N. N.; Surip, S. N.; Ratim, S.; Mahat, M. M.

    2012-06-01

    Hybridization of rubber toughened polyester-kenaf nanocomposite was prepared by adding various percentage of kenaf fiber with 4% Cloisite 30B in unsaturated polyester resin. Composite were prepared by adding filler to modified polyester resin subsequently cross-linked using methyl ethyl ketone peroxide and the accelerator cobalt octanoate 1%. Three per hundred rubbers (phr) of liquid natural rubber (LNR) were added in producing this composite. This composite expected to be applied in the interior of passenger cars and truck cabins. This is a quality local product from a combination of good properties polyester and high performance natural fiber, kenaf that is suitable for many applications such as in automotive sector and construction sector. The mechanical and thermal properties of composite were characterized using Durometer Shore-D hardness test, Izod impact test, Scanning electron microscopy, thermogravimetry (TGA) and differential scanning calorimetry (DSC). Result shows that addition of LNR give good properties on impact, flexural and hardness compare to without LNR composite. DSC curve shows that all composition of composites is fully cured and good in thermal properties. Addition of higher percentage of kenaf will lead the composite to elastic behavior and decrease the toughened properties of the composite. Hybrid system composite showed the flexural properties within the flexural properties of kenaf - polyester and Cloisite 30B.

  3. Liquefaction of corn stover and preparation of polyester from the liquefied polyol.

    Science.gov (United States)

    Yu, Fei; Liu, Yuhuan; Pan, Xuejun; Lin, Xiangyang; Liu, Chengmei; Chen, Paul; Ruan, Roger

    2006-01-01

    This research investigated a novel process to prepare polyester from corn stover through liquefaction and crosslinking processes. First, corn stover was liquefied in organic solvents (90 wt% ethylene glycol and 10 wt% ethylene carbonate) with catalysts at moderate temperature under atmospheric pressure. The effect of liquefaction temperature, biomass content, and type of catalyst, such as H2SO4, HCl, H3PO4, and ZnCl2, was evaluated. Higher liquefaction yield was achieved in 2 wt% sulfuric acid, 1/4 (w/w) stover to liquefying reagent ratio; 160 degrees C temperature, in 2 h. The liquefied corn stover was rich in polyols, which can be directly used as feedstock for making polymers without further separation or purification. Second, polyester was made from the liquefied corn stover by crosslinking with multifunctional carboxylic acids and/or cyclic acid anhydrides. The tensile strength of polyester is about 5 MPa and the elongation is around 35%. The polyester is stable in cold water and organic solvents and readily biodegradable as indicated by 82% weight loss when buried in damp soil for 10 mo. The results indicate that this novel polyester could be used for the biodegradable garden mulch film production.

  4. The Degradation of Mechanical Properties in Halloysite Nanoclay-Polyester Nanocomposites Exposed in Seawater Environment

    Directory of Open Access Journals (Sweden)

    Mohd Shahneel Saharudin

    2016-01-01

    Full Text Available Polyester based polymers are extensively used in aggressive marine environments; however, inadequate data is available on the effects of the seawater on the polyester based nanocomposites mechanical properties. This paper reports the effect of seawater absorption on the mechanical properties degradation of halloysite nanoclay-polyester nanocomposites. Results confirmed that the addition of halloysite nanoclay into polyester matrix was found to increase seawater uptake and reduce mechanical properties compared to monolithic polyester. The maximum decreases in microhardness, tensile and flexural properties, and impact toughness were observed in case of 1 wt% nanoclay. The microhardness decreased from 107 HV to 41.7 HV (61% decrease. Young’s modulus decreased from 0.6 GPa to 0.4 GPa (33% decrease. The flexural modulus decreased from 0.6 GPa to 0.34 GPa (43% decrease. The impact toughness dropped from 0.71 kJ/m2 to 0.48 kJ/m2 (32% decrease. Interestingly, the fracture toughness KIC increased with the addition of halloysite nanoclay due to the plasticization effect of the resin matrix. SEM images revealed the significant reduction in mechanical properties in case of 1 wt% reinforcement which is attributed to the degradation of the nanoclay-matrix interface influenced by seawater absorption and agglomeration of halloysite nanoclay.

  5. Recovery of Monomer from Nylon waste powder for its Recycling

    Directory of Open Access Journals (Sweden)

    Dilip B.Patil

    2014-03-01

    Full Text Available Recovery of monomer hexamethylene diamine(HMD in the form of dibenzoyl derivative of hexamethylene diamine (DBHMD from Nylon waste rope powder was carried out by degradation of Nylon waste powder of nylon rope waste.The molecular weight of nylon waste powder was found to be 26582.The minimum amount of nylon waste powder and hydrochloric acid required for maximum recovery of HMD and DBHMD was found to be 5g and 5N,50ml hydrochloric acid respectively. Further it was observed that the maximum time and temperature required for getting maximum yield of DBHMD was 120 minutes and 800C respectively.

  6. DDA Computations of Porous Aggregates with Forsterite Crystals: Effects of Crystal Shape and Crystal Mass Fraction

    Science.gov (United States)

    Wooden, Diane H.; Lindsay, Sean S.; Harker, David; Woodward, Charles; Kelley, Michael S.; Kolokolova, Ludmilla

    2015-01-01

    Porous aggregate grains are commonly found in cometary dust samples and are needed to model cometary IR spectral energy distributions (SEDs). Models for thermal emissions from comets require two forms of silicates: amorphous and crystalline. The dominant crystal resonances observed in comet SEDs are from Forsterite (Mg2SiO4). The mass fractions that are crystalline span a large range from 0.0 25 AU at 1E6 yr) by inner disk materials (crystals) are challenged to yield the highend-range of cometary crystal mass fractions. However, in current thermal models, Forsterite crystals are not incorporated into larger aggregate grains but instead only are considered as discrete crystals. A complicating factor is that Forsterite crystals with rectangular shapes better fit the observed spectral resonances in wavelength (11.0-11.15 microns, 16, 19, 23.5, 27, and 33 microns), feature asymmetry and relative height (Lindley et al. 2013) than spherically or elliptically shaped crystals. We present DDA-DDSCAT computations of IR absorptivities (Qabs) of 3 micron-radii porous aggregates with 0.13 crystals. We can produce crystal resonances with similar appearance to the observed resonances of comet Hale- Bopp. Also, a lower mass fraction of crystals in aggregates can produce the same spectral contrast as a higher mass fraction of discrete crystals; the 11micron and 23 micron crystalline resonances appear amplified when crystals are incorporated into aggregates composed otherwise of spherically shaped amorphous Fe-Mg olivines and pyroxenes. We show that the optical properties of a porous aggregate is not linear combination of its monomers, so aggregates need to be computed. We discuss the consequence of lowering comet crystal mass fractions by modeling IR SEDs with aggregates with crystals, and the implications for radial transport models of our protoplanetary disk.

  7. Comparison of monofunctional and multifunctional monomers in phosphate binding molecularly imprinted polymers.

    Science.gov (United States)

    Wu, Xiangyang; Goswami, Kisholoy; Shimizu, Ken D

    2008-01-01

    In this study, molecularly imprinted polymers (MIPs) prepared using a multifunctional and a monofunctional monomer were compared with respect to their affinities, selectivities, and imprinting efficiencies for organophosphates. This is of interest because multifunctional monomers have higher affinities than traditional monofunctional monomers for their target analytes and thus should yield MIPs with higher affinities and selectivities. However, polymers containing multifunctional monomer may also have a higher number of unselective, non-templated binding sites. This increase in background binding sites could lead to a decrease in the magnitude of the imprinting effect and in the selectivity of the MIP. Therefore, phosphate selective imprinted and non-imprinted polymers (NIPs) were prepared using a novel multifunctional triurea monomer. The binding properties of these polymers were compared with polymers prepared using a monofunctional monourea monomer. The binding affinities and selectivities of the monomers, imprinted polymers, and NIPs were characterized by NMR titration, binding uptake studies, and binding isotherms. MIPs prepared with the triurea monomer showed higher binding affinity and selectivity for the diphenylphosphate anion in organic solvents than the MIPs prepared with the monofunctional monomer. Surprisingly, the binding properties of the NIPs revealed that the polymers prepared using the multifunctional and monofunctional monomers were very similar in affinity and selectivity. Thus, the multifunctional monomers increase not only the affinity of the MIP but also enhance the imprinting effect.

  8. Synthesis of acrylic and allylic bifunctional cross-linking monomers derived from PET waste

    Science.gov (United States)

    Cruz-Aguilar, A.; Herrera-González, A. M.; Vázquez-García, R. A.; Navarro-Rodríguez, D.; Coreño, J.

    2013-06-01

    An acrylic and two novel allylic monomers synthesized from bis (hydroxyethyl) terephthalate, BHET, are reported. This was obtained by glycolysis of post-consumer PET with boiling ethylene glycol. The bifunctional monomer bis(2-(acryloyloxy)ethyl) terephthalate was obtained from acryloyl chloride, while the allylic monomers 2-(((allyloxi)carbonyl)oxy) ethyl (2-hydroxyethyl) terephthalate and bis(2-(((allyloxi)carbonyl)oxy)ethyl) terephthalate, from allyl chloroformate. Cross-linking was studied in bulk polymerization using two different thermal initiators. Monomers were analyzed by means of 1H NMR and the cross-linked polymers by infrared spectroscopy. Gel content higher than 90% was obtained for the acrylic monomer. In the case of the mixture of the allylic monomers, the cross-linked polymer was 80 % using BPO initiator, being this mixture 24 times less reactive than the acrylic monomer.

  9. 77 FR 4543 - Certain Polyester Staple Fiber From Taiwan: Extension of Time Limit for Preliminary Results of...

    Science.gov (United States)

    2012-01-30

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Certain Polyester Staple Fiber From Taiwan: Extension of Time Limit for... antidumping duty order on certain polyester staple fiber from Taiwan for the period May 1, 2010, through...

  10. 75 FR 70906 - Certain Polyester Staple Fiber From the People's Republic of China: Partial Rescission of the...

    Science.gov (United States)

    2010-11-19

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Certain Polyester Staple Fiber From the People's Republic of China: Partial... certain polyester staple fiber (``PSF'') from the People's Republic of China (``PRC'') for the period...

  11. 76 FR 5331 - Certain Polyester Staple Fiber From Taiwan: Extension of Time Limit for Preliminary Results of...

    Science.gov (United States)

    2011-01-31

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Certain Polyester Staple Fiber From Taiwan: Extension of Time Limit for... antidumping duty order on certain polyester staple fiber from Taiwan for the period May 1, 2009, through...

  12. 76 FR 69702 - Certain Polyester Staple Fiber From the People's Republic of China: Final Results of Antidumping...

    Science.gov (United States)

    2011-11-09

    ....20.0025 and known to the industry as polyester staple fiber for spinning and generally used in woven... carpeting; and (3) low-melt polyester staple fiber defined as a bi- component fiber with an outer, non... and non-PRC exporters not listed above that have separate rates, the cash deposit rate will...

  13. Effect of microheterogeneity on horse spleen apoferritin crystallization

    Science.gov (United States)

    Thomas, B. R.; Carter, D.; Rosenberger, F.

    1998-05-01

    Apoferritin (APO) is an interesting model protein for crystal growth studies, as an alternative to the widely used hen egg white lysozyme. The effect of naturally occurring oligomers on the crystallization of isolated, microhomogeneous APO monomers (24 subunits, Mr=440 000) was investigated. SDS PAGE analysis and immunoblotting showed that commercial APO was free of foreign proteins (>99.9% w/w). The quaternary structure of APO oligomers that form prior to the addition of precipitant was analyzed in native 4-15% T (1-2% C) gradient PAGE. Optical densitometry of these gels showed that oligomers (>24 subunit monomer) constituted approximately 45% w/w of the total APO. The primary oligomeric contaminants were dimers (48 subunits) with 35% w/w, and several bands constituting trimers (˜72 subunits) with 10% w/w. Directly determined physical molecular weights ( Mw) and conformational data for oligomers obtained by analytical gel filtration fast protein-liquid-chromatography separations utilizing UV and multi-angle laser light scattering detectors (GF-FPLC-MALLS) confirmed and expanded the native PAGE results. This technique allowed the discovery of large oligomers ( Mw=5 000 000 and 80 000 000) present in concentrations contamination to 5% w/w, and to produce 0.25 g of microhomogeneous monomers from 0.5 g APO. Crystallization from microhomogeneous monomer solutions yielded large crystals 0.5-1.0 mm in size. These crystals yielded an X-ray diffraction resolution of 1.8 Å. Reconstitutive experiments in which isolated oligomers were added to monomer preparations showed that dimers perturb the growth habit and reduce the crystal growth, without significantly affecting the nucleation. On trimer addition, the nucleation was increased and the crystal growth decreased. Addition of cadmium sulfate precipitant to unpurified APO did not affect the nature or quantity of the oligomers. These effects of oligomers on crystallization underline microheterogeneity as a

  14. Effects of acrylic resin monomers on porcine coronary artery reactivity.

    Science.gov (United States)

    Abebe, Worku; West, Daniel; Rueggeberg, Frederick A; Pashley, David; Mozaffari, Mahmood S

    2016-07-01

    The purpose of the present investigation was to assess the reactivity of porcine coronary arteries under in vitro conditions following their exposure to methyl methacrylate (MMA) and hydroxyethyl methacrylate (HEMA) monomers. Confirming previous studies using rat aortas, both MMA and HEMA induced acute/direct relaxation of coronary ring preparations, which was partly dependent on the endothelium. With prolonged tissue exposure, both monomers caused time- and concentration-dependent inhibition of receptor-mediated contraction of the vascular smooth muscle caused by prostaglandin F2∝ (PGF2∝), with HEMA causing more inhibition than MMA. Hydroxyethyl methacrylate, but not MMA, also produced impairment of non-receptor-mediated contraction of the coronary smooth muscle induced by KCl. On the other hand, neither HEMA nor MMA altered relaxation of the smooth muscle produced by the direct-acting pharmacological agent, sodium nitroprusside (SNP). While exposure to HEMA impaired endothelium-dependent vasorelaxation caused by bradykinin (BK), MMA markedly enhanced this endothelial-mediated response of the arteries. The enhanced endothelial response produced by MMA was linked to nitric oxide (NO) release. In conclusion, with prolonged tissue exposure, MMA causes less pronounced effects/adverse consequences on coronary smooth muscle function relative to the effect of HEMA, while enhancing vasorelaxation associated with release of NO from the endothelium. Accordingly, MMA-containing resin materials appear to be safer for human applications than materials containing HEMA.

  15. Wet air oxidation of epoxy acrylate monomer industrial wastewater.

    Science.gov (United States)

    Yang, Shaoxia; Liu, Zhengqian; Huang, Xiaohui; Zhang, Beiping

    2010-06-15

    Epoxy acrylate monomer industrial wastewater contained highly concentrated and toxic organic compounds. The wet air oxidation (WAO) and catalytic wet air oxidation (CWAO) were used to eliminate pollutants in order to examine the feasibility of the WAO/CWAO as a pre-treatment method for the industrial wastewater. The results showed that in the WAO 63% chemical oxygen demand (COD) and 41% total organic carbon (TOC) removals were achieved and biological oxygen demand (BOD(5))/COD ratio increased from 0.13 to 0.72 after 3h reaction at 250 degrees C, 3.5MPa and the initial concentration of 100g(COD)/L. Among homogenous catalysts (Cu(2+), Fe(2+), Fe(3+) and Mn(2+) salts), Cu(2+) salt exhibited better performance. CuO catalyst was used in the CWAO of the wastewater, COD and TOC conversion were 77 and 54%, and good biodegradability was achieved. The results proved that the CWAO was an effective pre-treatment method for the epoxy acrylate monomer industrial wastewater.

  16. Shelf Life of PMR Polyimide Monomer Solutions and Prepregs Extended

    Science.gov (United States)

    Alston, William B.; Scheiman, Daniel A.

    2000-01-01

    PMR (Polymerization of Monomeric Reactants) technology was developed in the mid-1970's at the NASA Glenn Research Center at Lewis Field for fabricating high-temperature stable polyimide composites. This technology allowed a solution of polyimide monomers or prepreg (a fiber, such as glass or graphite, impregnated with PMR polyimide monomers) to be thermally cured without the release of volatiles that cause the formation of voids unlike the non-PMR technology used for polyimide condensation type resins. The initial PMR resin introduced as PMR 15 is still commercially available and is used worldwide by aerospace industries as the state-of-the-art resin for high-temperature polyimide composite applications. PMR 15 offers easy composite processing, excellent composite mechanical property retention, a long lifetime at use temperatures of 500 to 550 F, and relatively low cost. Later, second-generation PMR resin versions, such as PMR II 50 and VCAP 75, offer improvements in the upper-use temperature (to 700 F) and in the useful life at temperature without major compromises in processing and property retention but with significant increases in resin cost. Newer versions of nontoxic (non-methylene dianiline) PMR resins, such as BAX PMR 15, offer similar advantages as originally found for PMR 15 but also with significant increases in resin cost. Thus, the current scope of the entire PMR technology available meets a wide range of aeronautical requirements for polymer composite applications.

  17. Effect of cationic monomer on properties of fluorinated acrylate latex

    Institute of Scientific and Technical Information of China (English)

    Li Jun Chen

    2012-01-01

    Cationic fluorinated acrylate latex was prepared via semi-continuous emulsion copolymerization of cationic monomer and other monomers.The resultant latex and its film were characterized with dynamic light scattering detector and contact angle meter.Influences of amount of DMDAAC on the properties of resultant latex and its film were investigated in detail.Results show that the particle size of the latex has the minimum value and the zeta potential of the latex is increased when the amount of DMDAAC is increased.In addition,the particle size of the latex is unimodal distribution when the amount of DMDAAC is not more than 2.5%.However,the particle size of the latex is bimodal distribution when the amount of DMDAAC is more than 2.5%.The contact angle is varied slightly with the increase of amount of DMDAAC when it is not more than 2.5%.Nevertheless,the contact angle is decreased with the increase of the amount of DMDAAC when it is more than 25%.

  18. Induced DNA damage by dental resin monomers in somatic cells.

    Science.gov (United States)

    Arossi, Guilherme Anziliero; Lehmann, Mauricio; Dihl, Rafael Rodrigues; Reguly, Maria Luiza; de Andrade, Heloisa Helena Rodrigues

    2010-02-01

    The present in vivo study investigated the genotoxicity of four dental resin monomers: triethyleneglycoldimethacrylate (TEGDMA), hydroxyethylmethacrylate (HEMA), urethanedimethacrylate (UDMA) and bisphenol A-glycidylmethacrylate (BisGMA). The Somatic Mutation and Recombination Test (SMART) in Drosophila melanogaster was applied to analyse their genotoxicity expressed as homologous mitotic recombination, point and chromosomal mutation. SMART detects the loss of heterozygosity of marker genes expressed phenotypically on the fly's wings. This fruit fly has an extensive genetic homology to mammalians, which makes it a suitable model organism for genotoxic investigations. The present findings provide evidence that the mechanistic basis underlying the genotoxicity of UDMA and TEGDMA is related to homologous recombination and gene/chromosomal mutation. A genotoxic pattern can correspondingly be discerned for both UDMA and TEGDMA: their genotoxicity is attributed respectively to 49% and 44% of mitotic recombination, as well as 51% and 56% of mutational events, including point and chromosomal alterations. The monomer UDMA is 1.6 times more active than TEGDMA to induce mutant clones per treatment unit. BisGMA and HEMA had no statistically significant effect on total spot frequencies - suggesting no genotoxic action in the SMART assay. The clinical significance of these observations has to be interpreted for data obtained in other bioassays.

  19. The Kinetics of Cellulose Grafting with Vinyl Acetate Monomer

    Directory of Open Access Journals (Sweden)

    Éva Borbély

    2005-11-01

    Full Text Available Cellulose is a natural raw material recurring in a great quantity. The demand touse it more and more widely is increasing. The production of cellulose derivates started asearly as the 19th century, however the modification of these materials meant the breakingup the fibrous structure, which made their use more difficult in paper industry. Themodified cellulose made by graft copolymerization, however, keeps its fibrous character,which provides a great advantage regarding its use. Grafting of industrial cellulose pulpwith vinyl-acetate allows for the production of grafted wood cellulose fibres that have athermoplastic layer on their surface. The binder fibre (fibrid produced in this way can beexcellently used for producing synthetic papers.In the first part of my experiments I dealt with choosing the parameters of graftcopolymerization which are best suited to various uses and after that I studied thedependence of graft reaction on the composition and properties of industrial celluloseapplied. The selection of the suitable reaction parameters was followed by the study ofreaction speed and activation energy. I have stated that the gross reaction of graftingindustrial cellulose with vinyl-acetate monomer is a second order reaction, which is provenby the fact that the invert of the momentary monomer concentration of the system plottedagainst time is a linear function. The rise of the curves, that is, the reaction speed increaseswhen the temperature in the range of 293–323 K is increasing, while the average activationenergy decreases.

  20. Thermotropic liquid crystalline polyesters derived from bis-(4-hydroxybenzoyloxy)-2-methyl-1,4-benzene and aliphatic dicarboxylic acid chlorides

    Indian Academy of Sciences (India)

    Khudbudin Mulani; Mohasin Momin; Nitin Ganjave; Nayaku Chavan

    2015-09-01

    A series of thermotropic liquid crystalline polyesters derived from bis-(4-hydroxybenzoyloxy)-2-methyl-1,4-benzene (BHBOMB) and aliphatic dicarboxylic acid chlorides were investigated. All these polyesters were synthesized by interfacial polycondensation method and characterized by differential scanning calorimetry and wide-angle X-ray diffractometer. These polyesters consist of BHBOMB as a mesogenic diol and aliphatic diacid chlorides were used as flexible spacers. The length of oligomethylene units in polymer was varied from the trimethylene to the dodecamethylene groups. The transition temperatures and thermodynamic properties were studied for all these polymers. All these polyesters were soluble in chlorinated solvents such as chloroform, dichloromethane, dichloroethane, etc. More importantly, all these polyesters exhibited very large mesophase stability.

  1. Photoinduced anisotropy in a family of amorphous azobenzene polyesters for optical storage

    DEFF Research Database (Denmark)

    Nedelchev, Lian; Matharu, Avtar S.; Hvilsted, Søren

    2003-01-01

    We investigate parameters associated with optical data storage in a variety of amorphous side-chain azobenzene-containing polyesters denoted as E1aX. The polyesters possess a common cyano-substituted azobenzene chromophore as a side chain, but differ in their main-chain polyester composition....... Seventeen different polymers from the E1aX family divided into four classes, depending on the type of the main-chain substituent (one-, two-, and three-ring aromatic or alicyclic) have been thoroughly investigated. Various parameters characterizing the photoinduced birefringence in these materials...... of E1aX polymers characterized by two-ring aromatic substituent in the main chain is a good candidate for optical data storage media. A recording energy of approximately 2 J/cm(2) is sufficient to induce high refractive-index modulations of Deltan = 0.13 in these materials, which is retained even...

  2. Synthesis and Characterization of Anionic Polyester-Polyurethane Dispersion as Environmentally-Friendly Waterbased Resins

    Directory of Open Access Journals (Sweden)

    Najaf i F. Manouchehri F., and Shaabanz

    2012-01-01

    Full Text Available Aqueous polyurethane dispersions (PUDs have recently emerged as important alternatives to their solvent-based counterparts for various applications due to increasing health and environmental awareness (green chemistry. Anionic polyester-polyurethane dispersions were synthesized by three steps. In the first step, macromonomer diisocyanate having carboxylic acid was prepared by isophorone diisocyanate (IPDI, dimethylol propionic acid (DMPA in percent of acetone as solvent and dibutyldtin dilaurate (DBTDL as catalyst. Then, carboxylic polyurethane was prepared by reaction macromonomer diisocyanate having carboxylic acid with linear aliphatic polyester (Mw=2000, trifunctional polyester (Mw=2800 and butanediol (BDO as chain extender. The next step involved neutralization and dispersion in water, where acidic polyurethane was neutralized by the addition of triethylamine (TEA.  Factors influencing the synthesis of polyurethane dispersion mainly involve reaction temperature, reaction time, the concentration of catalyst, DMPA content and BDO content, were studied. The polymers have been characterized with DSC and FTIR.

  3. Ammonium Y zeolite applied as a thermochemolysis reagent for identification of polyethers and polyesters.

    Science.gov (United States)

    Blazsó, Marianne; Bozi, János

    2013-01-04

    A potential thermochemolysis reagent has been tested for the pyrolysis gas chromatographic identification of polyether, polyester and polyether- or polyester-based thermoplastic polyurethane. The main advantage of ammonium Y zeolite over liquid reagents is that it does not react prior to pyrolysis, and its reactions have no incomplete products. The procedure of the thermochemolysis is as simple as running a pyrolysis-GC/MS analysis sampling a powder mixture of roughly equal mass of polymer and ammonium Y zeolite. The GC/MS chromatograms obtained show that the products of thermochemolysis are specific to the diol and dicarboxylic units of the polymer. It was observed that ethanal or 1,4-dioxane forms from ethylene oxide components of polyethers and polyesters, tetrahydrofuran from butylene oxide units, hexanedinitrile from adipate groups, and benzodinitrile from terephthalate groups.

  4. A model for biodegradation of composite materials made of polyesters and tricalcium phosphates.

    Science.gov (United States)

    Pan, Jingzhe; Han, Xiaoxiao; Niu, Wenjuan; Cameron, Ruth E

    2011-03-01

    A saturation behaviour has been observed when incorporating tricalcium phosphate (TCP) in various polyesters to control the degradation rate. This paper presents an understanding of this behaviour using a mathematical model. The coupled process of hydrolysis reaction of the ester bonds, acid dissociation of the carboxylic end groups, dissolution of the calcium phosphates and buffering reactions by the dissolved phosphate ions is modelled together using a set of differential equations. Two non-dimensional groups of the material and chemical parameters are identified which control the degradation rate of the composites. An effectiveness map is established to show the conditions under which incorporating TCP into polyesters is effective, saturated or ineffective. Comparisons are made between the model predictions and existing experimental data in the literature. The map provides a useful tool to guide the design of polyester/TCP composites for tissue engineering and orthopaedic fixation applications.

  5. Tribological Behaviour of E-Glass /Epoxy & E-Glass /polyester Composites for Automotive Body Application

    Directory of Open Access Journals (Sweden)

    Esmael Adem

    2015-10-01

    Full Text Available Experimental characterization of the mechanical properties of E-glass/Epoxy & Eglass/Polyester composite was conducted. The objectives of this paper is to present processing techniques of specimen preparation, conducting experiment to obtain mechanical properties and conduct experimental observation using Scanning Electron Microscopy (SEM to know in homogeneity, porosity and fracture behavior. The effect of strain rate on E-glass/epoxy and E-glass/polyester has been investigated & experimentation was performed to determine property data for material specifications. E-glass/polyester laminates were obtained by compression moulding process and E-glass/epoxy laminate by hand lay-up vacuum assisted technique. The laminates were cut to obtain ASTM standards. This investigation deals with the testing of tensile, compression, shear and flexural strength on a universal testing machine. The graphs that are obtained from the tests were documented. This research indicates that the mechanical properties are mainly dependent on the strain rate.

  6. 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.

  7. Nature Inspired Solutions for Polymers: Will Cutinase Enzymes Make Polyesters and Polyamides Greener?

    Directory of Open Access Journals (Sweden)

    Valerio Ferrario

    2016-12-01

    Full Text Available The polymer and plastic sectors are under the urge of mitigating their environmental impact. The need for novel and more benign catalysts for polyester synthesis or targeted functionalization led, in recent years, to an increasing interest towards cutinases due to their natural ability to hydrolyze ester bonds in cutin, a natural polymer. In this review, the most recent advances in the synthesis and hydrolysis of various classes of polyesters and polyamides are discussed with a critical focus on the actual perspectives of applying enzymatic technologies for practical industrial purposes. More specifically, cutinase enzymes are compared to lipases and, in particular, to lipase B from Candida antarctica, the biocatalyst most widely employed in polymer chemistry so far. Computational and bioinformatics studies suggest that the natural role of cutinases in attacking natural polymers confer some essential features for processing also synthetic polyesters and polyamides.

  8. Synthesis and characterization of saturated polyester and nanocomposites derived from glycolyzed PET waste with varied compositions

    Indian Academy of Sciences (India)

    Sunain Katoch; Vinay Sharma; P P Kundu

    2013-04-01

    Saturated polyester resin, derived from the glycolysis of polyethyleneterephthalate (PET) was examined as an effective way for PET recycling. The glycolyzed PET (GPET) was reacted with the mixture of phthalic anhydride and ethylene glycol (EG) with varied compositions and their reaction kinetic were studied. During polyesterification of GPET, acid and EG, the parameters like degree of polymerization (DP), extent of reaction () acid value and hydroxyl values were measured. The thermomechanical properties and the morphologies of the saturated polyester nanocomposites were examined by using a differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), wide angle X-ray diffraction (WAXRD) and transmission electron spectroscopy (TEM). There were significant differences observed in g, m and c before and after addition of GPET and clay content. Nanocomposites with lower content of organoclay showed intercalated morphology while by increasing the amount of organoclay, the exfoliated morphology was more prevalent. Water vapour transmission (WVT) was determined for saturated polyester nanocomposite sheets according to ASTM E96-80.

  9. Crystallization and crystal manipulation of the Pterocarpus angolensis seed lectin.

    Science.gov (United States)

    Loris, Remy; Garcia-Pino, Abel; Buts, Lieven; Bouckaert, Julie; Beeckmans, Sonia; De Greve, Henri; Wyns, Lode

    2005-06-01

    The Man/Glc-specific legume lectin from the seeds of the African bloodwood tree (Pterocarpus angolensis) was crystallized in the presence of the disaccharide ligand Man(alpha1-3)ManMe. Small crystals initially appeared from a preliminary screen, but proved difficult to reproduce. The initial crystals were used to prepare microseeds, leading to a reproducible crystallization protocol. All attempts to obtain crystals directly of the ligand-free protein or of other carbohydrate complexes failed. However, the Man(alpha1-3)ManMe co-crystals withstand soaking with ten other carbohydrates known to bind to the lectin. Soaking for 15 min in 100 mM carbohydrate typically resulted in complete replacement of Man(alpha1-3)ManMe by the desired carbohydrate despite the involvement of lattice contacts at the binding site. Transferring the crystals for two weeks in carbohydrate-free artificial mother liquor resulted in the complete removal of the sugar from one of the two monomers in the asymmetric unit. Additional treatment of these crystals with 100 mM EDTA for two weeks resulted in removal of the structural calcium and manganese ions, which is accompanied by significant structural rearrangements of the loops that constitute the carbohydrate-binding site.

  10. Approach to formation of multifunctional polyester particles in controlled nanoscopic dimensions.

    Science.gov (United States)

    van der Ende, Alice E; Kravitz, Evan J; Harth, Eva

    2008-07-09

    We present the synthesis of discrete functionalized polyester nanoparticles in selected nanoscale size dimensions via a controlled intermolecular chain cross-linking process. The novel technique involves the controlled coupling of epoxide functionalized polyesters with 2,2'-(ethylenedioxy)bis(ethylamine) to give well-defined nanoparticles with narrow size distribution and selected nanoscopic size dimensions. Diverse functionalized polyesters, synthesized with pendant functionalities via ring-opening copolymerization of delta-valerolactone with alpha-allyl-delta-valerolactone, alpha-propargyl-delta-valerolactone and 2-oxepane-1,5-dione, were prepared as linear precursors which facilitated 3-D nanoparticles with functionalities such as amines, keto groups, and alkynes for post modification reactions. We found that the nanoparticle formation and the control over the nanoscopic dimension is primarily influenced by the degree of the epoxide entity implemented in the precursor polymers and the amount of 2,2'-(ethylenedioxy)bis(ethylamine) as cross-linking reagent. The other functionalities in the linear polyester do not participate in the nanoparticle formation and particles with defined functionalities can be prepared from batches of identical linear polymers containing various functionalities or by mixing different polyester materials to achieve controlled amounts of specific functional groups. The utilization of integrated functionalities was demonstrated in one post-modification reaction with N-Boc-ethylenediamine via reductive amination. This work describes the development of a novel methodology to prepare functionalized well-defined 3-D nanoparticle polyester materials in targeted nanoscopic ranges with amorphous morphologies or tailored crystallinities that offer a multitude of utilizations as a result of their unique properties and control in preparation.

  11. Análise de peças anatômicas preservadas com resina de poliester para estudo em anatomia humana Analysis of anatomical pieces preservation with polyester resin for human anatomy study

    Directory of Open Access Journals (Sweden)

    Ítalo Martins de Oliveira

    2013-02-01

    Full Text Available OBJETIVO: avaliar o uso da resina de poliéster na preservação de peças anatômicas para estudo da anatomia humana. MÉTODOS: foram utilizadas 150 peças anatômicas, sendo as mesmas não fixadas (frescas, fixadas em formol a 10% e moldes vasculares de órgãos injetados com acetato de vinil e a resina de poliéster. A solução utilizada foi composta de resina de poliéster com seu diluente monômero de estireno e catalisador (peroxol. Foram obtidos, após a inclusão nesta solução, modelos em resina transparente, que permitiam a plena observação das estruturas e conservação da peça utilizada. RESULTADOS: na avaliação das peças, foi observado grau de extrema transparência, promovendo uma completa visualização das estruturas com a perfeita preservação da anatomia. A duração média para a completa finalização da inclusão foi 48 horas. Apenas 14 peças (9,3% foram inutilizadas durante o preparo. CONCLUSÃO: a resina de poliéster pode ser utilizada para a preservação de peças anatômicas para o ensino da anatomia humana, de maneira prática, estética e duradoura.OBJECTIVE: To evaluate the use of polyester resin in preserving anatomical specimens for the study of human anatomy. METHODS: We used 150 anatomical specimens, comprised of unfixed (fresh, fixed in 10% formalin and vascular casts of organs injected with vinyl acetate and polyester resin. The solution used consisted of polyester resin with the diluent styrene monomer and catalyst (peroxol. After embedding in this solution, models in transparent resin were obtained, allowing full observation of structures and conservation of the specimens used. RESULTS: upon evaluation of the specimens, we observed a high degree of transparency, which promoted a complete visualization of structures with perfect preservation of the anatomy. The average time for the completion of the embedding was 48 hours. Only 14 specimens (9.3% were lost during the preparation. CONCLUSION

  12. Flexible polyester cellulose paper supercapacitor with a gel electrolyte.

    Science.gov (United States)

    Karthika, Prasannan; Rajalakshmi, Natarajan; Dhathathreyan, Kaveripatnam S

    2013-11-11

    A low-cost polyester cellulose paper has been used as a substrate for a flexible supercapacitor device that contains aqueous carbon nanotube ink as the electrodes and a polyvinyl alcohol (PVA)-based gel as the electrolyte. Gel electrolytes have attracted much interest due to their solvent-holding capacity and good film-forming capability. The electrodes are characterized for their conductivity and morphology. Because of its high conductivity, the conductive paper is studied in supercapacitor applications as active electrodes and as separators after coating with polyvinylidene fluoride. Carbon nanotubes deposited on porous paper are more accessible to ions in the electrolyte than those on flat substrates, which results in higher power density. A simple fabrication process is achieved and paper supercapacitors are tested for their performance in both aqueous and PVA gel electrolytes by using galvanostatic and cyclic voltammetry methods. A high specific capacitance of 270 F g(-1) and an energy density value of 37 W h kg(-1) are achieved for devices with PVA gel electrolytes. Furthermore, this device can maintain excellent specific capacitance even under high currents. This is also confirmed by another counter experiment with aqueous sulfuric acid as the electrolyte. The cycle life, one of the most critical parameters in supercapacitor operations, is found to be excellent (6000 cycles) and less than 0.5 % capacitance loss is observed. Moreover, the supercapacitor device is flexible and even after twisting does not show any cracks or evidence of breakage, and shows almost the same specific capacitance of 267 F g(-1) and energy density of 37 W h kg(-1) . This work suggests that a paper substrate can be a highly scalable and low-cost solution for high-performance supercapacitors.

  13. Preliminary Discussion on Improving Tensile Strength of Polyester Bulked Continuous Filament%提高涤纶膨体变形长丝断裂强度初探

    Institute of Scientific and Technical Information of China (English)

    胡子坡

    2013-01-01

    Polyester (PET) bulked continuous filament (BCF) is made on the imported special spinning machine with conventional PET chips.The PET BCF with tensile strength higher than 2.5 cN/dtex is obtained by selecting suitable PET chips,optimum pre-crystallization and drying process,proper spinning temperature,improving drawing unit and process.%采用常规聚酯(PET)切片为原料,在进口专用纺丝机上生产PET膨体变形长丝(BCF).选择合适的聚酯切片,优选预结晶和干燥工艺,合理设计纺丝温度,改进牵伸装置,优化牵伸工艺,生产出断裂强度大于2.5 cN/dtex的PET BCF.

  14. Surface modification of polyester film by glow discharge tunnel at atmospheric pressure

    Institute of Scientific and Technical Information of China (English)

    XU Xiang-yu; WANG Shou-guo; YE Tian-chun; JING Guang-yin; YU Da-peng

    2004-01-01

    A large-area improved dielectric barrier glow discharge tunnel has been developed for modifying the surface of polyester film at atmospheric pressure with argon and oxygen gas mixtures. The electrical properties of the glow discharge tunnel were studied by simultaneous measurement of the voltage and current. In addition, the effect of the glow discharge tunnel treatment on the surface of polyester film were studied. The resultant modifications of the surface properties of the treated samples were investigated through scanning probe microscopy and contact angle measurement.

  15. Synthesis of lipase-catalysed silicone-polyesters and silicone-polyamides at elevated temperatures.

    Science.gov (United States)

    Frampton, Mark B; Zelisko, Paul M

    2013-10-18

    More and more enzymes are being explored as alternatives to conventional catalysts in chemical reactions. To utilize these biocatalysts to their fullest, it is incumbent on researchers to gain a complete understanding of the reaction conditions that particular enzymes will tolerate. To this end siloxane-containing polyesters and polyamides have been produced via N435-mediated catalysis at temperatures well above the normal denaturation temperature for free CalB. Low molecular weight disiloxane-based acceptors release the enzyme from its acylated state with equal proficiency while longer chain siloxanes favours polyester synthesis. The thermal tolerance of the enzyme catalyst is increased using longer chain diesters and generally more hydrophobic substrates.

  16. Sound Absorbing Property of Porous Material by Using Polyester Fiber Waste

    Science.gov (United States)

    Kurahashi, Naoya; Kimura, Teruo

    Polyester waste generated from a water jet loom in the weaving process is one of the typical industrial fiber wastes. The development of a recycling system for such fiber wastes has been strongly expected so far. In this study, the recyclability of polyester wastes as a sound absorption material was discussed. As a result, it was cleared that the sound absorption material can be obtained by heated compression molding combined with a PLA binder and fiber wastes, and higher sound absorption properties are obtainable if the defiberization of the waste is increased.

  17. Measurement of salivary cortisol--effects of replacing polyester with cotton and switching antibody

    DEFF Research Database (Denmark)

    Hansen, Ase Marie; Garde, Anne Helene; Persson, Roger;

    2008-01-01

    measurements in our laboratory were affected by: 1) changes in the tampon material and 2) changes in the antibody of the analytical kit. In study 1, saliva from healthy subjects (n = 19) was split and spiked to Salivette polyester and cotton tampons, respectively, and treated as ordinary samples before being...... analysed for cortisol using a Spectria RIA kit for cortisol. In study 2, 68 anonymous saliva samples were analysed with the Spectria Cortisol RIA kit both before and after the manufacturer changed the antibody. The change from polyester to cotton tampons reduced the measured concentration of salivary...

  18. Towards a Guided Regeneration of Renal Tubules at a Polyester Interstitium

    Directory of Open Access Journals (Sweden)

    Will W. Minuth

    2010-03-01

    Full Text Available Stem/progenitor cells are promising candidates for a therapy of renal failure. However, sound knowledge about implantation and regeneration is lacking. Therefore, mechanisms leading from stem/progenitor cells into tubules are under research. Renal stem/progenitor cells were isolated from neonatal rabbit kidney and mounted between layers of polyester fleece. It creates an artificial interstitium and replaces coating by extracellular matrix proteins. Tubulogenic development is induced by aldosterone. Electron microscopy illuminates growth of tubules in close vicinity to polyester fibers. Tubules contain a differentiated epithelium. The spatial extension of tubules opens a new strategy for testing morphogenic drugs and biocompatible fleece materials.

  19. STUDY ON SOME PROPERTIES OF Si-CONTAINING POLYESTER-POLYETHER MULTIBLOCK COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    LI Zhenyi; ZHU Jin

    1997-01-01

    Some physical properties of the polyester-polyether multiblock copolymers with Si-containing hard segment were further examined by a series of physical methods. The hydrophobicity of the copolymers was improved with the incorporation of increasing amount of orgauosilicone, XPS test proved that silicon element was enriched at the surface of the Si-containing polyester-polyether copolymers. It was also found that their heat resistance and gas permeability for O2 and N2 were greatly improved. The study on semipermeability of films made of the Si-containing copolymers was also followed with interest.

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

    DEFF Research Database (Denmark)

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

    2001-01-01

    that the formation of the surface relief is dependent on the substituents. In both experiments irradiation with p-polarized light generates peaks for the CN, CF3, CH3 and F substituents, while fur a Cl substituent valleys art: observed. Also s-polarized light is found to produce surface deformations. An amorphous...... azobenzene polyester was included in the study for comparison. The results point to a mechanism of the surface relief phenomenon, in which the architecture of the polyesters plays a crucial role....