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Sample records for a-533-824 polyethylene terephthalate

  1. Profiles in garbage: Polyethylene terephthalate

    SciTech Connect

    Miller, C.

    1997-11-01

    Polyethylene terephthalate (PET) is a plastic resin used primarily to make bottles. Soft drinks -- along with salad dressing, fruit juices, peanut butter, and other household and consumer products -- use PET bottles. PET also is used for film, sheeting for cups and food trays, oven-safe trays, and other uses. PET is a relatively new packaging resin, first commercialized in the early 1970s. Because it is an ``engineered`` resin, PET is more expensive than commodity resins such as high-density polyethylene (HDPE) and, for the same reason, it is usually the highest valued plastic recyclable.

  2. Waste product profile: Polyethylene terephthalate

    SciTech Connect

    Miller, C.

    1996-02-01

    Polyethylene terephthalate (PET) is a plastic resin used primarily to make bottles. Soft drinks are the primary product packaged in PET. Salad dressing, peanut butter, and other household and consumer products also use PET bottles. PET is also used for film, sheeting for cups and food trays, ovenable trays, and other uses. PET is a relatively new packaging resin, first commercialized in the early `70s. Because it is an ``engineered`` resin, it is more expensive than commodity resins such as high-density polyethylene (HDPE). The primary market for recycled PET is the fiber industry, which uses PET for carpet fiber, sweaters and other clothing, and for other uses. Recycled PET can also be used for food and beverage containers. Export markets, particularly Asian countries, are becoming increasingly important.

  3. Speciation of antimony in polyethylene terephthalate bottles

    SciTech Connect

    Martin, R.R.; Ablett, J.; Shotyk, W.S.; Naftel, S.; Northrup, P.

    2009-12-18

    Antimony contamination has been reported in drinking water from polyethylene terephthalate (PET) bottles. Micro-X-ray fluorescence (XRF) analysis has been used to identify the distribution and chemical form of residual antimony used as a catalyst in the manufacture of PET bottles. The results are consistent with clusters of Sb(III) having dimensions of the order of tens of micrometers, clearly showing the ability of synchrotron radiation analyses to both map elemental distribution and determine oxidation state.

  4. 21 CFR 870.3470 - Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or...

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. 870.3470 Section 870.3470 Food and Drugs... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. (a) Identification. An intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene is a...

  5. 21 CFR 870.3470 - Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or...

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. 870.3470 Section 870.3470 Food and Drugs... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. (a) Identification. An intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene is a...

  6. 21 CFR 870.3470 - Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or...

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. 870.3470 Section 870.3470 Food and Drugs... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. (a) Identification. An intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene is a...

  7. 21 CFR 870.3470 - Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or...

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. 870.3470 Section 870.3470 Food and Drugs... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. (a) Identification. An intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene is a...

  8. 21 CFR 870.3470 - Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or...

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. 870.3470 Section 870.3470 Food and Drugs... polypropylene, polyethylene terephthalate, or polytetrafluoroethylene. (a) Identification. An intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene is a...

  9. Depolymerization of polyethylene terephthalate in supercritical methanol

    NASA Astrophysics Data System (ADS)

    Goto, Motonobu; Koyamoto, Hiroshi; Kodama, Akio; Hirose, Tsutomu; Nagaoka, Shoji

    2002-11-01

    The degradation of polyethylene terephthalate (PET) in supercritical methanol was investigated with the aim of developing a process for chemical recycling of waste plastics. A batch reactor was used at temperatures of 573-623 K under an estimated pressure of 20 MPa for a reaction time of 2-120 min. PET was decomposed to its monomers, dimethyl terephthalate and ethylene glycol, by methanolysis in supercritical methanol. The reaction products were analysed using size-exclusion chromatography, gas chromatography-mass spectrometry, and reversed-phase liquid chromatography. The molecular weight distribution of the products was obtained as a function of reaction time. The yields of monomer components of the decomposition products including by-products were measured. Continuous kinetics analysis was performed on the experimental data.

  10. Polyethylene terephthalate thin films; a luminescence study

    NASA Astrophysics Data System (ADS)

    Carmona-Téllez, S.; Alarcón-Flores, G.; Meza-Rocha, A.; Zaleta-Alejandre, E.; Aguilar-Futis, M.; Murrieta S, H.; Falcony, C.

    2015-04-01

    Polyethylene Terephthalate (PET) films doped with Rare Earths (RE3+) have been deposited on glass by spray pyrolysis technique at 240 °C, using recycled PET and (RE3+) chlorides as precursors. Cerium, terbium, dysprosium and europium were used as dopants materials, these dopants normally produce luminescent emissions at 450, 545, 573 and 612 nm respectively; the doped films also have light emissions at blue, green, yellow and red respectively. All RE3+ characteristic emissions were observed at naked eyes. Every deposited films show a high transmission in the visible range (close 80% T), films surfaces are pretty soft and homogeneous. Films thickness is around 3 μm.

  11. Investigation of Raman spectra of polyethylene terephthalate

    NASA Astrophysics Data System (ADS)

    Zhu, Changjun; Tong, Na; Song, Lixin; Zhang, Guoqing

    2015-08-01

    Raman spectrometry was employed to study the characteristics of Raman spectra of polyethylene terephthalate (PET), which were treated with sodium hydroxide, sulfuric acid and copper sulfate, respectively. Raman spectra under different conditions were obtained and the characteristics of the Raman spectra were analyzed. The morphology structures were observed under different conditions using Atomic Force Microscope. The results show that the spectral intensity of PET treated with sodium hydroxide is higher than that untreated between 200-1750 cm-1, while the intensity of PET treated with sodium hydroxide is lower than that untreated beyond 1750 cm-1 and the fluorescence background of Raman spectra is decreased. The spectral intensity of PET treated with sulfuric acid is remarkably reduced than that untreated, and the intensity of PET treated with copper sulphate is much higher than that untreated.

  12. [Characteristics of Raman Spectra of Polyethylene Terephthalate].

    PubMed

    Tong, Na; Zhu, Chang-jun; Song, Li-xun; Zhang, Chong-hui; Zhang, Guo-qing; Zhang, Yi-xin

    2016-01-01

    Raman spectrometry was employed to study the characteristics of Raman spectra of polyethylene terephthalate (PET), which were treated with sodium hydroxide, sulfuric acid and copper sulfate, respectively. Raman spectra under different conditions were obtained and the characteristics of the Raman spectra were analyzed. The morphology structures were observed under different conditions using Atomic Force Microscope. The results show that the spectral intensity of PET treated with sodium hydroxide is higher than that untreated between 200-1 750 cm(-1), while the intensity of PET treated with sodium hydroxide is lower than that untreated beyond 1 750 cm(-1) and the fluorescence background of Raman spectra is decreased. The spectral intensity of PET treated with sulfuric acid is remarkably reduced than that untreated, and the intensity of PET treated with copper sulphate is much higher than that untreated. The research results obtained by Atomic Force Microscopy show that the variations of the Raman spectra of PET fibers are closely related to. the chemical bonds and molecular structures of PET fibers. The surface of the PET treated with sodium hydroxide is rougher than that untreated, the surface roughness of the PET treated with sulfuric acid is reduced as compared to that untreated, while the surface roughness of the PET treated with copper sulphate is increased. The results obtained by Raman spectroscopy are consistent with those by Atomic Force Microscopy, indicating that the combination of Raman spectroscopy and Atomic Force Microscopy is expected to be a promising characterization technology for polymer characteristics. PMID:27228752

  13. Organocatalytic decomposition of polyethylene terephthalate using triazabicyclodecene

    NASA Astrophysics Data System (ADS)

    Lecuyer, Julien Matsumoto

    This study focuses on the organocatalytic decomposition of polyethylene terephthalate (PET) using 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) to form a diverse library of aromatic amides. The reaction scheme was specifically designed to use low reaction temperatures (>150°C) and avoid using solvents during the reaction to provide a more environmentally friendly process. Of all the amines tested, PET aminolysis with aliphatic and aromatic amines demonstrated the best performance with yields higher than 72%. PET aminolysis with click functionalized and non-symmetric reagents facilitated attack on certain sites on the basis of reactivity. Finally, the performance of the PET degradation reactions with secondary amine and tertiary amine functionalized reagents yielded mixed results due to complications with isolating the product from the crude solution. Four of the PET-based monomers were also selected as modifiers for epoxy hardening to demonstrate the ability to convert waste into monomers for high-value applications. The glass transition temperatures, obtained using differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) of the epoxy composite samples treated with the PET-based monomers, were generally higher in comparison to the samples cured with the basic diamines due to the hydrogen bonding and added rigidity from the aromatic amide group. Developing these monomers provides a green and commercially viable alternative to eradicating a waste product that is becoming an environmental concern.

  14. 75 FR 52717 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-27

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... polyethylene terephthalate film, sheet and strip from India for the period January 1, 2009 through December 31, 2009. See Polyethylene Terephthalate Film, Sheet and Strip from India: Initiation of Antidumping...

  15. A bacterium that degrades and assimilates poly(ethylene terephthalate).

    PubMed

    Yoshida, Shosuke; Hiraga, Kazumi; Takehana, Toshihiko; Taniguchi, Ikuo; Yamaji, Hironao; Maeda, Yasuhito; Toyohara, Kiyotsuna; Miyamoto, Kenji; Kimura, Yoshiharu; Oda, Kohei

    2016-03-11

    Poly(ethylene terephthalate) (PET) is used extensively worldwide in plastic products, and its accumulation in the environment has become a global concern. Because the ability to enzymatically degrade PET has been thought to be limited to a few fungal species, biodegradation is not yet a viable remediation or recycling strategy. By screening natural microbial communities exposed to PET in the environment, we isolated a novel bacterium, Ideonella sakaiensis 201-F6, that is able to use PET as its major energy and carbon source. When grown on PET, this strain produces two enzymes capable of hydrolyzing PET and the reaction intermediate, mono(2-hydroxyethyl) terephthalic acid. Both enzymes are required to enzymatically convert PET efficiently into its two environmentally benign monomers, terephthalic acid and ethylene glycol. PMID:26965627

  16. Ultrasound-enhanced enzymatic hydrolysis of poly(ethylene terephthalate).

    PubMed

    Pellis, Alessandro; Gamerith, Caroline; Ghazaryan, Gagik; Ortner, Andreas; Herrero Acero, Enrique; Guebitz, Georg M

    2016-10-01

    The application of ultrasound was found to enhance enzymatic hydrolysis of poly(ethylene terephthalate) (PET). After a short activation phase up to 6.6times increase in the amount of released products was found. PET powder with lower crystallinity of 8% was hydrolyzed faster when compared to PET with 28% crystallinity. Ultrasound activation was found to be around three times more effective on powders vs. films most likely due to a larger surface area accessible to the enzyme. PMID:27481467

  17. Chemical Recycling of Pop Bottles: The Synthesis of Dibenzyl Terephthalate from the Plastic Polyethylene Terephthalate

    NASA Astrophysics Data System (ADS)

    Donahue, Craig J.; Exline, Jennifer A.; Warner, Cynthia

    2003-01-01

    A laboratory procedure involving the chemical recycling of the plastic polyethylene terephthalate (PET or PETE) from 2-L pop bottles is described. A transesterification reaction is employed to depolymerize PET. At atmospheric pressure in refluxing benzyl alcohol in the presence of a catalyst, PET is converted to dibenzyl terephthalate in moderate yields. This procedure models an industrial process that involves the transesterification reaction of PET with methanol at high temperature and pressure, conditions not normally accessible in an undergraduate laboratory, to yield dimethyl terephthalate and ethylene glycol. A second method of preparing dibenzyl terephthalate starting with terephthaloyl chloride is also described. The diester from these two approaches is characterized using melting points, TLC, and IR and NMR spectroscopy. This experiment has been used in a general chemistry sequence that has sections on organic chemistry and polymer chemistry, but is also well suited for an introductory organic chemistry laboratory course or a polymer chemistry laboratory course. This lab experiment is part of a larger effort to develop a general chemistry sequence for engineering students using the theme of chemistry and the automobile. Student results are presented.

  18. A novel preparation of milk protein/polyethylene terephthalate fabric

    NASA Astrophysics Data System (ADS)

    Zhou, J. F.; Zheng, D. D.; Zhong, L.; Zhang, F. X.; Zhang, G. X.

    2016-07-01

    In this work, -NH2 groups were introduced to polyethylene terephthalate (PET) fibers by nitration and reduction method, and then milk protein was grafted on the nitrated and reduced PET (NR PET) fibers by sucrose glycidyl ether crosslinking agent. FTIR suggested the milk protein was successfully grafted on PET fiber surface. SEM images showed a layer of substance covered on the PET fiber surface. DSC demonstrated an excellent thermal stability of milk protein/PET fiber. The moisture regain was improved by milk protein/PET fiber. Moreover, the crease recovery angle and stiffness were retained by the milk protein/PET fabric.

  19. 76 FR 75870 - Polyethylene Terephthalate Film, Sheet, and Strip From Korea: Notice of Rescission of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-05

    ..., 76 FR 45227 (July 28, 2011) (Initiation Notice). \\2\\ See Polyethylene Terephthalate Film, Sheet, and Strip from Korea: Final Results of Antidumping Duty Administrative Review and Revocation in Part, 76 FR... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Korea: Notice...

  20. 75 FR 10758 - Polyethylene Terephthalate Film, Sheet and Strip from India: Initiation of Antidumping Duty and...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-09

    ... Order: Polyethylene Terephthalate Film, Sheet and Strip (PET Film) from India, 67 FR 44179 (July 1, 2002... India, 67 FR 44175 (July 1, 2002) (Antidumping Duty Order). The notice announcing the countervailing... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip from India: Initiation...

  1. 78 FR 79400 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Initiation...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-12-30

    ... and Amended Final Determination of Sales at Less Than Fair Value for the United Arab Emirates, 73 FR... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic... a request for a new shipper review of the antidumping duty order on polyethylene terephthalate...

  2. 78 FR 2365 - Polyethylene Terephthalate Film, Sheet and Strip From India: Partial Rescission of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-11

    ... Administrative Review, 77 FR 39216, 39217 (July 2, 2012). \\2\\ Petitioners are DuPont Teijin Films, Mitsubishi..., 77 FR 52688 (August 30, 2012). \\6\\ See Polyethylene Terephthalate (PET) Film, Sheet, and Strip from... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India:...

  3. 78 FR 42105 - Polyethylene Terephthalate Film, Sheet, and Strip From India and Taiwan; Notice of Commission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-07-15

    ... COMMISSION Polyethylene Terephthalate Film, Sheet, and Strip From India and Taiwan; Notice of Commission... countervailing duty order on polyethylene terephthalate film, sheet, and strip (``PET'' film) from India and the antidumping duty orders on PET film from India and Taiwan would be likely to lead to continuation...

  4. 78 FR 47276 - Polyethylene Terephthalate (PET) Film, Sheet, and Strip From India: Final Results of the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-05

    ...: Polyethylene Terephthalate Film, Sheet, and Strip From India, 67 FR 44179 (July 1, 2002). On April 2, 2012, the... 1930, as amended (the Act). See Initiation of Five-Year (``Sunset'') Reviews, 78 FR 19647 (April 2... International Trade Administration Polyethylene Terephthalate (PET) Film, Sheet, and Strip From India:...

  5. Polymeric cracking of waste polyethylene terephthalate to chemicals and energy.

    PubMed

    Brems, Anke; Baeyens, Jan; Vandecasteele, Carlo; Dewil, Raf

    2011-07-01

    Polyethylene terephthalate (PET) is a widely used thermoplastic. PET residues represent on average 7.6 wt% of the different polymer wastes in Europe. Pyrolysis of these wastes is attracting increasing interest, and PET is a potential candidate for this thermal process. The paper measures and discusses the kinetics of the pyrolysis reaction in terms of the reaction rate constants as determined by dynamic thermogravimetric analysis, with special emphasis on the required heating rate to obtain relevant results. The product yields and compositions are also determined. Gaseous products represent 16-18 wt%. The amounts of condensables and carbonaceous residue are a function of the operating mode, with slow pyrolysis producing up to 24 wt% of carbonaceous residue. Major condensable components are benzoic acid, monovinyl terephthalate, divinyl terephthalate, vinyl benzoate, and benzene. The present paper complements previous literature findings by (1) the study of the influence of the heating rate on the reaction kinetics in dynamic pyrolysis tests, (2) the isothermal investigation in a fluidized bed reactor to pyrolyze PET, and (3) the assessment of upgrading and recovery of the products. The paper concludes with a proposed reactor recommendation for PET pyrolysis, in either the bubbling or circulating fluidized bed operating mode. PMID:21850826

  6. Properties of Poly (ethylene terephthalate) / Poly(ethylene terephthalate-co-4,4'bibenzoate) Blends

    NASA Astrophysics Data System (ADS)

    Kumar, Satish; Min, Byung-Gil; Schiraldi, David; Collard, David; Hibbs, Michael; Zhou, Chongfu; Ma, Hongming

    2002-03-01

    A blend of poly (ethylene terephthalate) (PET) and a semi-rigid poly(ethylene terephthalate-co-4,4'bibenzoate) (PETBB55), containing 55 mole terephthalate, was melt processed using a twin screw extruder at 285^oC with a resident time of 100 seconds and the PET to PETBB55 blend ratio was 70:30. ^13C NMR spectroscopy showed that little or no transesterification occurred during extrusion due to the short residence time. However, the as-blended sample is optically transparent and exhibited only one Tg. The blend also exhibited only one Tm at 245^oC, which is lower than the Tm for PET (255^oC) as well as that for PETBB55 (259^oC). The Tm further decreased by keeping the polymer for longer time in the melt state, and finally approached a value of 220^oC and at this sate the blend has transesterified to a completely random copolymer as observed by ^13C NMR. The as-blended chip showed much slower crystallization than PET and showed a minimum isothermal crystallization rate at 155^oC when cooled from the melt. The isothermally crystallized sample showed a secondary endothermic peak just above the crystallization temperature but well below Tm. This peaks has been studied using modulated Differential Scanning Calorimetery. The blend has been melt spun into fibers with a modulus higher than that of PET.

  7. [Polyethylene terephthalate (PET)--health aspects and food packaging application].

    PubMed

    Cwiek-Ludwicka, Kazimiera

    2003-01-01

    Polyethylene terephthalate (PET) due to its physicochemical properties, especially regidity and glass-like transparency is widely used as food packaging material. The relevant legislation states that substances may not migrate from food contacting materials in quantities that may cause undesirable changes in organoleptic properties of food coming into contact with such material. The lists of substances authorized for food contact plastic materials and requirements for the final product were established. The requirements concern global migration limits (60 mg/kg or 10 mg/dm2) and specific migration limits (SML) set for substances which, when migrate into food in grater quantities may cause risk for human health. For the products manufactured from PET the specific migration limits were set for terephthalic acid (7.5 mg/kg), for isophthalic acid (5 mg/kg), for isophthalic acid dimethyl ester (0.05 mg/kg) and for ethylene and diethylene glycol (30 mg/kg). PET may undergo thermal degradation resulting in formation of acetaldehyde, which may influence organoleptic characteristics of packaged foods changing taste and smell. PMID:14531083

  8. Dimensionally stable PET fibers for tire reinforcement. [Polyethylene terephthalate (POLYESTERS)

    SciTech Connect

    Rim, P.B.; Nelson, C.J.

    1991-05-01

    High-modulus, high-tenacity polyethylene terephthalate (PET) fibers have gained wide acceptance in reinforcement for rubber products such as tires and hoses; in geotextiles, and in ropes and cordage. Accordingly, a great deal of fundamental research has been conducted on how the processing and resulting morphology of these thermoplastic fibers affect their physical properties. The translation of these starting fiber properties to those in the final end-use product has received much less attention. This article compares the structure-property relationships of recently-developed PET yarns possessing high dimensional stability (i.e., high modulus and low shrinkage) with conventional PET tire yarn. Interest in these materials is stimulated by their ability to improve tire uniformity and, for some tire manufacturers, eliminate the need for post-cure inflation during tire manufacturing. Where possible, cause and effect relationships will be developed.

  9. Texturation and superhydrophobicity of polyethylene terephthalate thanks to plasma technology

    NASA Astrophysics Data System (ADS)

    Tarrade, Jeanne; Darmanin, Thierry; Taffin de Givenchy, Elisabeth; Guittard, Frédéric; Debarnot, Dominique; Poncin-Epaillard, Fabienne

    2014-02-01

    Anti-bioadhesive surfaces were designed from polyethylene terephthalate (PET) by three steps plasma-treatment. First, the nano-pattern is created by oxygen plasma-treatment with controlled dimensions. Then, the plasma-treated polymeric surface was hydrophobized with a tetrafluorocarbon plasma, allowing to obtain a water contact angle of 145 ± 4°. However, the SEM pictures give evidence to show the degradation of the structuration caused by the CF4-plasma and consequently, the superhydrophobicity was not reached. Thus, a plasma-polypyrrole layer was deposited before the plasma-fluorination, which has a protective role against the degradation generated by fluorinated species, preserving the structuration and improving the fluorination rate. Therefore, the obtained surfaces are superhydrophobic with water contact angle of 157 ± 2° and a hysteresis of 65 ± 3°. The ability of these surfaces to reduce bioadhesion will be performed in further work.

  10. Gel permeation chromatography (GPC) of repeatedly extruded polyethylene terephthalate (PET).

    PubMed

    Milana, M R; Denaro, M; Arrivabene, L; Maggio, A; Gramiccioni, L

    1998-04-01

    The paper deals with gel permeation chromatography (GPC) monitoring of the behaviour of PET (polyethylene terephthalate) after repeated extrusions. Virgin PET was submitted to three successive extrusion/drying cycles and then the samples were swelled with hexafluoroisopropanol and treated with chloroform. GPC analysis was carried out at room temperature on a B.C.S. Serial LC 2000 GPC system equipped with a series of four GPC columns with UV detection at 254 nm and chloroform as eluent. GPC results showed that after each extrusion step the molecular weight distribution of the PET was different and Mw, Mn and Mz decreased. These findings suggest that during each extrusion degradation occurs and that repeated extrusions, as in the case of the recycling PET, may cause an alteration of the molecular weight distribution of the original PET. PMID:9666895

  11. 76 FR 57715 - Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea: Revocation of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-16

    ... Terephthalate Film, Sheet, and Strip From the Republic of Korea, 56 FR 25669 (June 5, 1991). On September 1... film from the Republic of Korea. See Initiation of Five-Year (``Sunset'') Review, 75 FR 53664... reasonably foreseeable time. See Polyethylene Terephthalate (PET) Film From Korea, 76 FR 54791 (September...

  12. 75 FR 75172 - Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-02

    ... FR 49900 (August 16, 2010) (Preliminary Results). This administrative review covers one respondent... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Final Results... terephthalate film, sheet, and strip (PET film) from Brazil for the period November 6, 2008, through October...

  13. 76 FR 39855 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-07

    ... Order, Finding, or Suspended Investigation; Opportunity to Request an Administrative Review, 75 FR 38074... Countervailing Duty Administrative Reviews and Deferral of Initiation of Administrative Review, 75 FR 53274... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission,...

  14. 76 FR 39855 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-07

    ... Duty Order, Finding, or Suspended Investigation; Opportunity to Request an Administrative Review, 75 FR... Countervailing Duty Administrative Reviews and Deferral of Initiation of Administrative Review, 75 FR 53274... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission,...

  15. Histological characteristics and ultrastructure of polyethylene terephthalate LARS ligament after the reconstruction of anterior cruciate ligament in rabbits

    PubMed Central

    Yu, Shao-Bin; Yang, Rong-Hua; Zuo, Zhong-Nan; Dong, Qi-Rong

    2014-01-01

    Polyethylene terephthalate LARS ligament were the remnant of LARS ligament used for repairing posterior cruciate ligament obtained from operation. We want to study histological characteristics and ultrastructure of polyethylene terephthalate LARS ligament after the reconstruction of anterior cruciate ligament in rabbits. Therefore, we replaced the original ACL with polyethylene terephthalate LARS ligament which was covering with the remnant of ACL in 9 rabbits (L-LARS group), while just only polyethylene terephthalate LARS ligament were transplanted in 3 rabbits (LARS group) with the remnant of ACL. Compared with group LARS, inflammatory cell reaction and foreign body reaction were more significant in group L-LARS. Moreover, electron microscopy investigation showed the tissue near LARS fibers was highly cellular with a matrix of thin collagen fibrils (50-100 nm) in group L-LARS. These above findings suggest the polyethylene terephthalate LARS ligament possess the high biocompatibility, which contributes to the polyethylene terephthalate LARS covered with recipient connective tissues. PMID:25356104

  16. Solvent-Induced Crystallization in Poly(Ethylene Terephthalate)

    NASA Astrophysics Data System (ADS)

    Ouyang, Hao

    2000-03-01

    The solvent transport in poly(ethylene terephthalate) (PET) and related phase transformation were investigated. Based on Harmon's model for Case I (Fickian), Case II (swelling) and anomalous transport, the data of mass uptake were analyzed. Pure Case I or Case II behavior did not appear in the PET-acetone system. The mass transport in PET is accompanied by a large-scale structural rearrangement, which leads to the induced crystallization of the original amorphous state. Solvent-induced crystallization was studied by wide angle X-ray scattering (WAXS), small angle x-ray scattering (SAXS), Differential Scanning Calorimeter (DSC), and Fourier Transform Infra-Red (FTIR), which is different from the thermal crystallization. During this process, the matrix is under compressive stress which causes different kinetic path of crystallization in comparison with that by thermal annealing. The crystallization process was proposed in terms of the long period L, the crystal thickness lc and the thickness of amorphous layer la, calculated from the linear correlation function and interface distribution function. The variation of trans conformation is used to monitor this process.

  17. Robust identification of polyethylene terephthalate (PET) plastics through Bayesian decision.

    PubMed

    Zulkifley, Mohd Asyraf; Mustafa, Mohd Marzuki; Hussain, Aini; Mustapha, Aouache; Ramli, Suzaimah

    2014-01-01

    Recycling is one of the most efficient methods for environmental friendly waste management. Among municipal wastes, plastics are the most common material that can be easily recycled and polyethylene terephthalate (PET) is one of its major types. PET material is used in consumer goods packaging such as drinking bottles, toiletry containers, food packaging and many more. Usually, a recycling process is tailored to a specific material for optimal purification and decontamination to obtain high grade recyclable material. The quantity and quality of the sorting process are limited by the capacity of human workers that suffer from fatigue and boredom. Several automated sorting systems have been proposed in the literature that include using chemical, proximity and vision sensors. The main advantages of vision based sensors are its environmentally friendly approach, non-intrusive detection and capability of high throughput. However, the existing methods rely heavily on deterministic approaches that make them less accurate as the variations in PET plastic waste appearance are too high. We proposed a probabilistic approach of modeling the PET material by analyzing the reflection region and its surrounding. Three parameters are modeled by Gaussian and exponential distributions: color, size and distance of the reflection region. The final classification is made through a supervised training method of likelihood ratio test. The main novelty of the proposed method is the probabilistic approach in integrating various PET material signatures that are contaminated by stains under constant lighting changes. The system is evaluated by using four performance metrics: precision, recall, accuracy and error. Our system performed the best in all evaluation metrics compared to the benchmark methods. The system can be further improved by fusing all neighborhood information in decision making and by implementing the system in a graphics processing unit for faster processing speed. PMID

  18. Robust Identification of Polyethylene Terephthalate (PET) Plastics through Bayesian Decision

    PubMed Central

    Zulkifley, Mohd Asyraf; Mustafa, Mohd Marzuki; Hussain, Aini; Mustapha, Aouache; Ramli, Suzaimah

    2014-01-01

    Recycling is one of the most efficient methods for environmental friendly waste management. Among municipal wastes, plastics are the most common material that can be easily recycled and polyethylene terephthalate (PET) is one of its major types. PET material is used in consumer goods packaging such as drinking bottles, toiletry containers, food packaging and many more. Usually, a recycling process is tailored to a specific material for optimal purification and decontamination to obtain high grade recyclable material. The quantity and quality of the sorting process are limited by the capacity of human workers that suffer from fatigue and boredom. Several automated sorting systems have been proposed in the literature that include using chemical, proximity and vision sensors. The main advantages of vision based sensors are its environmentally friendly approach, non-intrusive detection and capability of high throughput. However, the existing methods rely heavily on deterministic approaches that make them less accurate as the variations in PET plastic waste appearance are too high. We proposed a probabilistic approach of modeling the PET material by analyzing the reflection region and its surrounding. Three parameters are modeled by Gaussian and exponential distributions: color, size and distance of the reflection region. The final classification is made through a supervised training method of likelihood ratio test. The main novelty of the proposed method is the probabilistic approach in integrating various PET material signatures that are contaminated by stains under constant lighting changes. The system is evaluated by using four performance metrics: precision, recall, accuracy and error. Our system performed the best in all evaluation metrics compared to the benchmark methods. The system can be further improved by fusing all neighborhood information in decision making and by implementing the system in a graphics processing unit for faster processing speed. PMID

  19. Solar Disinfection of Viruses in Polyethylene Terephthalate Bottles

    PubMed Central

    Carratalà, Anna; Dionisio Calado, Alex; Mattle, Michael J.; Meierhofer, Regula; Luzi, Samuel

    2015-01-01

    Solar disinfection (SODIS) of drinking water in polyethylene terephthalate (PET) bottles is a simple, efficient point-of-use technique for the inactivation of many bacterial pathogens. In contrast, the efficiency of SODIS against viruses is not well known. In this work, we studied the inactivation of bacteriophages (MS2 and ϕX174) and human viruses (echovirus 11 and adenovirus type 2) by SODIS. We conducted experiments in PET bottles exposed to (simulated) sunlight at different temperatures (15, 22, 26, and 40°C) and in water sources of diverse compositions and origins (India and Switzerland). Good inactivation of MS2 (>6-log inactivation after exposure to a total fluence of 1.34 kJ/cm2) was achieved in Swiss tap water at 22°C, while less-efficient inactivation was observed in Indian waters and for echovirus (1.5-log inactivation at the same fluence). The DNA viruses studied, ϕX174 and adenovirus, were resistant to SODIS, and the inactivation observed was equivalent to that occurring in the dark. High temperatures enhanced MS2 inactivation substantially; at 40°C, 3-log inactivation was achieved in Swiss tap water after exposure to a fluence of only 0.18 kJ/cm2. Overall, our findings demonstrate that SODIS may reduce the load of single-stranded RNA (ssRNA) viruses, such as echoviruses, particularly at high temperatures and in photoreactive matrices. In contrast, complementary measures may be needed to ensure efficient inactivation during SODIS of DNA viruses resistant to oxidation. PMID:26497451

  20. 75 FR 40776 - Polyethylene Terephthalate Film, Sheet and Strip From the United Arab Emirates: Extension of Time...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-07-14

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From the United Arab... of the antidumping duty order on polyethylene terephthalate film, sheet and strip from the United... Antidumping and Countervailing Duty Administrative Reviews and Requests for Revocation in Part, 74 FR...

  1. 75 FR 76954 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Extension of Time Limit for Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-10

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Extension of... Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary Results of Antidumping Duty Administrative Review, 75 FR 49902 (August 16, 2010) (Preliminary Results). The review covers the period July...

  2. 76 FR 45508 - Polyethylene Terephthalate Film, Sheet and Strip From the United Arab Emirates: Extension of Time...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-29

    ... Antidumping and Countervailing Duty Administrative Reviews and Request for Revocation in Part, 75 FR 81565... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From the United Arab... of the antidumping duty order on polyethylene terephthalate film, sheet and strip from the...

  3. Enhancing the Dyeability of Polypropylene Fibers by Melt Blending with Polyethylene Terephthalate

    PubMed Central

    Moradian, Siamak; Ameri, Farhad

    2013-01-01

    Attempts were made to modify polypropylene fibers by melt blending with polyethylene terephthalate in order to enhance the dyeability of the resultant fiber. Five blends of polypropylene/polyethylene terephthalate/compatibilizer were prepared and subsequently spun into fibers. Three disperse dyes were used to dye such modified fibers at boiling and 130°C. The dyeing performance of the blend fibers, as well as the morphological, chemical, thermal, and mechanical properties, of the corresponding blends was characterized by means of spectrophotometry, polarized optical microscopy, scanning electron microscopy (SEM), FT-IR spectroscopy, differential scanning calorimetry (DSC), and tensile testing. PMID:24288485

  4. Modification of polyethylene terephthalate track membrane properties by ammonia plasma

    NASA Astrophysics Data System (ADS)

    Kravets, Lyubov; Dmitriev, Serguei; Dinescu, George; Lazea, Andrada; Raiciu, Eric

    2004-09-01

    The properties of polyethylene terephthalate track membranes (PET TM) exposed to ammonia are investigated. The influence of the conditions of plasma treatment on the basic characteristics of the membranes, namely pore size and shape, wettability, water permeability, is studied. PET TM of the thickness of 10 μ m with the effective pore diameter of 0.215 μ m (pore density 2\\cdot 10^8 cm-2) were under study. The plasma treatment was performed on a plasma-chemical installation realizing a RF-discharge on the frequency 13.56 MHz. The process was conducted in a dynamic mode. Before delivering vapours of the plasma forming gas, the chamber was beforehand vacuumed down to residual pressure of 10-2 Torr. One side of the membranes was subjected to plasma. The discharge parameters (gas pressure in the vacuum chamber, discharge power) and the duration of plasma action were varied. It has been figured out that when treating the membranes in plasma of the explored gas there are two competing processes: etching of a polymeric matrix and deposition of a polymeric layer on their surface. It has been shown that at a short time of plasma action and low values of the discharge parameters, an etching process is mainly observed. Decrease in the thickness of the membranes and increase in the effective pore diameter testifies it. A result of the gas-discharge etching is also a hydrophilization of the TM surface stipulated by formation of polar function groups in the points of breaking chemical bonds. Here the value of the water contact angle of surface decreases down to 45-50 degrees in some cases. It has been shown that at a longer action of the plasma and increase of the discharge parameters, as accumulation in the chamber of etch products takes place, a process of deposition of a polymeric film becomes dominating, and it is proved by increasing the width of the membranes and changing their color. The value of the water contact angle of surface in this case is grown and, depending

  5. Remote atmospheric-pressure plasma activation of the surfaces of polyethylene terephthalate and polyethylene naphthalate.

    PubMed

    Gonzalez, E; Barankin, M D; Guschl, P C; Hicks, R F

    2008-11-01

    The surfaces of poly(ethylene terephthalate) (PET) and poly(ethylene naphthalate) (PEN) were treated with an atmospheric-pressure oxygen and helium plasma. Changes in the energy, adhesion, and chemical composition of the surfaces were determined by contact angle measurements, mechanical pull tests, and X-ray photoelectron spectroscopy (XPS). Surface-energy calculations revealed that after plasma treatment the polarity of PET and PEN increased 6 and 10 times, respectively. In addition, adhesive bond strengths were enhanced by up to 7 times. For PET and PEN, XPS revealed an 18-29% decrease in the area of the C 1s peak at 285 eV, which is attributable to the aromatic carbon atoms. The C 1s peak area due to ester carbon atoms increased by 11 and 24% for PET and PEN, respectively, while the C 1s peak area resulting from C-O species increased by about 5% for both polymers. These results indicate that oxygen atoms generated in the plasma rapidly oxidize the aromatic rings on the polymer chains. The Langmuir adsorption rate constants for oxidizing the polymer surfaces were 15.6 and 4.6 s(-1) for PET and PEN, respectively. PMID:18834154

  6. 76 FR 76948 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results of Countervailing...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-09

    ... Administrative Review, 76 FR 47558 (August 5, 2011) (Preliminary Results), the following events have occurred... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results... strip (PET Film) from India for Ester Industries Ltd. (Ester), covering the period of review (POR)...

  7. 78 FR 48147 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-07

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary... film, sheet and strip (PET film) from India for the period of review (POR) January 1, 2011, through... Strip from India (Preliminary Decision Memorandum), dated concurrently with these results and...

  8. Comment on "A bacterium that degrades and assimilates poly(ethylene terephthalate)".

    PubMed

    Yang, Yu; Yang, Jun; Jiang, Lei

    2016-08-19

    Yoshida et al (Report, 11 March 2016, p. 1196) reported that the bacterium Ideonella sakaiensis 201-F6 can degrade and assimilate poly(ethylene terephthalate) (PET). However, the authors exaggerated degradation efficiency using a low-crystallinity PET and presented no straightforward experiments to verify depolymerization and assimilation of PET. Thus, the authors' conclusions are rather misleading. PMID:27540159

  9. Dielectric properties of film materials based on polyethylene terephthalate and polycarbonate with ferroelectric inclusions

    NASA Astrophysics Data System (ADS)

    Golitsyna, O. M.; Drozhdin, S. N.

    2012-08-01

    The dielectric properties of film materials based on polyethylene terephthalate and polycarbonate with inclusions of triglycine sulfate (TGS) and TGS with admixture of L, α-alanine (ATGS) have been studied. An increase in the temperature of the phase transition in these materials as compared to in bulk TGS and ATGS has been revealed.

  10. 75 FR 49902 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-16

    ..., Notice of Final Determination of Sales at Less Than Fair Value: 67 FR 35474, May 20, 2002. See also.... See Antidumping Proceedings: Affiliated Party Sales in the Ordinary Course of Trade, 67 FR 69186...: Polyethylene Terephthalate Film, Sheet, and Strip (PET Film) from Taiwan, 67 FR 46566 (July 1, 2002). On July...

  11. The Depolymerization of Poly(Ethylene Terephthalate) (PET) Using N-Heterocyclic Carbenes from Ionic Liquids

    ERIC Educational Resources Information Center

    Kamber, Nahrain E.; Tsujii, Yasuhito; Keets, Kate; Waymouth, Robert M.; Pratt, Russell C.; Nyce, Gregory W.; Hedrick, James L.

    2010-01-01

    The depolymerization of the plastic polyethylene terephthalate (PET or PETE) is described in this laboratory procedure. The transesterification reaction used to depolymerize PET employs a highly efficient N-heterocyclic carbene catalyst derived from a commercially available imidazolium ionic liquid. N-heterocyclic carbenes are potent nucleophilic…

  12. 78 FR 77649 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates; Preliminary...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-12-24

    ... Assessment Rate in Certain Antidumping Proceedings: Final Modification, 77 FR 8101 (February 14, 2012). The... Than Fair Value for the United Arab Emirates, 73 FR 66595, 66597 (November 10, 2008). Notification to... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United...

  13. 76 FR 58244 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-20

    ...; Opportunity To Request Administrative Review, 76 FR 38609, 38610 (July 1, 2010). The Department received a... Initiation of Administrative Review, 76 FR 53404 (August 26, 2011). On August 23, 2011, Vacmet and Polypacks... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission,...

  14. 76 FR 18156 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-01

    ... Deferral of Initiation of Administrative Review, 75 FR 53274 (August 31, 2010). The Department initiated... for Administrative Determination Deadlines Pursuant to the Tariff Act of 1930, As Amended, 70 FR 24533... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension...

  15. 76 FR 58248 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, In Part, of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-20

    ... Suspended Investigation; Opportunity To Request Administrative Review, 76 FR 38609, 38610 (July 1, 2011... Revocation in Part, 76 FR 53404 (August 26, 2011). On August 23, 2011, Vacmet and Polypacks withdrew their... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission,...

  16. 75 FR 14423 - Polyethylene Terephthalate Film, Sheet and Strip from Taiwan: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-25

    ... Revocation in Part, 74 FR 42873 (August 25, 2009). This review covers two producers and/or exporters of the... Act of 1930, As Amended, 70 FR 24533 (May 10, 2005). Accordingly, the deadline for the completion of... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip from Taiwan: Extension...

  17. 78 FR 2369 - Polyethylene Terephthalate Film, Sheet and Strip From India: Partial Rescission of Countervailing...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-11

    ... Duty Order, Finding, or Suspended Investigation; Opportunity To Request Administrative Review, 77 FR... Administrative Reviews and Requests for Revocation in Part, 77 FR 52688 (August 30, 2012). Rescission, in Part... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India:...

  18. 76 FR 18155 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-01

    ... Administrative Review, 75 FR 53274 (August 31, 2010). The Department initiated the review with respect to two..., As Amended, 70 FR 24533 (May 10, 2005). Accordingly, the deadline for the completion of the... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension...

  19. 76 FR 48122 - Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-08

    ... FR 67079 (November 1, 2010). On November 30, 2010, DuPont Teijin Films, Mitsubishi Polyester Film... Sales at Less Than Fair Value: Polyethylene Terephthalate Film, Sheet, and Strip from Brazil, 73 FR... Emirates, 73 FR 66595 (November 10, 2008). On November 1, 2010, the Department published Antidumping...

  20. 78 FR 67113 - Polyethylene Terephthalate Film, Sheet and Strip From India and Taiwan: Preliminary Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-11-08

    ... Value and Antidumping Duty Order: Polyethylene Terephthalate Film, Sheet, and Strip from India, 67 FR... Second Antidumping Duty Sunset Reviews 78 FR 45512 (July 29, 2013) (``PET Film Extension Notice''). \\5...) from Taiwan, 67 FR 44174 (July 1, 2002). \\2\\ See Initiation of Five-Year (``Sunset'') Review, 78...

  1. 77 FR 76456 - Polyethylene Terephthalate Film, Sheet and Strip from Taiwan: Partial Rescission of the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-28

    ..., Finding, or Suspended Investigation; Opportunity To Request Administrative Review, 77 FR 39216, 39217... Reviews and Requests for Revocation in Part, 77 FR 52688 (August 30, 2012). Rescission, In Part Pursuant... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip from Taiwan:...

  2. 76 FR 42113 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Extension...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-18

    ... Revocation in Part, 75 FR 81565 (December 28, 2010). The preliminary results of this review are currently due... the Tariff Act of 1930, as Amended, 70 FR 24533 (May 10, 2005). Accordingly, the deadline for... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's...

  3. 21 CFR 878.5000 - Nonabsorbable poly(ethylene terephthalate) surgical suture.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Nonabsorbable poly(ethylene terephthalate) surgical suture. 878.5000 Section 878.5000 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF... thread prepared from fibers of high molecular weight, long-chain, linear polyesters having...

  4. 21 CFR 878.5000 - Nonabsorbable poly(ethylene terephthalate) surgical suture.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Nonabsorbable poly(ethylene terephthalate) surgical suture. 878.5000 Section 878.5000 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF... thread prepared from fibers of high molecular weight, long-chain, linear polyesters having...

  5. 21 CFR 878.5000 - Nonabsorbable poly(ethylene terephthalate) surgical suture.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Nonabsorbable poly(ethylene terephthalate) surgical suture. 878.5000 Section 878.5000 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF... thread prepared from fibers of high molecular weight, long-chain, linear polyesters having...

  6. 21 CFR 878.5000 - Nonabsorbable poly(ethylene terephthalate) surgical suture.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Nonabsorbable poly(ethylene terephthalate) surgical suture. 878.5000 Section 878.5000 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF... thread prepared from fibers of high molecular weight, long-chain, linear polyesters having...

  7. 21 CFR 878.5000 - Nonabsorbable poly(ethylene terephthalate) surgical suture.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Nonabsorbable poly(ethylene terephthalate) surgical suture. 878.5000 Section 878.5000 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF... thread prepared from fibers of high molecular weight, long-chain, linear polyesters having...

  8. 78 FR 45512 - Polyethylene Terephthalate Film from India and Taiwan: Extension of Time Limits for Preliminary...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-07-29

    ... 1930, As Amended, 70 FR 24533 (May 10, 2005). Extension Of Time Limits In accordance with section 751(c... International Trade Administration Polyethylene Terephthalate Film from India and Taiwan: Extension of Time...'') Review, 78 FR 19647 (April 2, 2013). Within the deadline specified in 19 CFR 351.218(d)(1)(i),...

  9. 75 FR 81574 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-28

    ...The Department of Commerce (the Department) is conducting a new shipper review under the countervailing duty (CVD) order on polyethylene terephthalate film, sheet and strip (PET film) from India in response to a request from SRF Limited (SRF). The period of review (POR) is January 1, 2009, through December 31, 2009. The domestic interested parties for this proceeding are DuPont Teijin Films,......

  10. Evaluating fibrous polyethylene terephthalate (PET) and cellulose as components for soilless substrates

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The objective of this work was to test the suitability of FiberFill, a synthetic fiber made of polyethylene terephthalate, and Tencel, a cellulose-based fiber, as growing mix components by evaluating the growth of a variety of floriculture crops using substrates containing different proportions of t...

  11. Evaluating Performance and Stability of Polyethylene Terephthalate (PET) and Cellulose Polymer as Soilless Mix Components

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In the U.S., concerns over the long-term sustainability of peat, perlite, and other media components have led to searches for alternative materials. FiberFill, a synthetic fiber made of recyclable polyethylene terephthalate, and Tencel, a cellulose fiber, are new materials with potential as substra...

  12. 76 FR 40325 - Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea: Preliminary Results...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-08

    ...The Department of Commerce (the Department) is conducting an administrative review of the antidumping duty order on polyethylene terephthalate film, sheet and strip (PET film) from the Republic of Korea (Korea). This review covers one company, Kolon Industries Inc. (Kolon) for the period of review (POR) of June 1, 2009, through May 31, 2010. We preliminarily determine that Kolon has made sales......

  13. 75 FR 49900 - Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-16

    ...The Department of Commerce (the Department) is conducting an administrative review of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET film) from Brazil. This administrative review covers one respondent, Terphane, Inc. (Terphane) and the period of review (POR) is November 6, 2008 through October 31, 2009. Given Terphane's failure to respond to the......

  14. Supercritical methanol for polyethylene terephthalate depolymerization: observation using simulator.

    PubMed

    Genta, Minoru; Iwaya, Tomoko; Sasaki, Mitsuru; Goto, Motonobu

    2007-01-01

    To apply PET depolymerization in supercritical methanol to commercial recycling, the benefits of supercritical methanol usage in PET depolymerization was investigated from the viewpoint of the reaction rate and energy demands. PET was depolymerized in a batch reactor at 573 K in supercritical methanol under 14.7 MPa and in vapor methanol under 0.98 MPa in our previous work. The main products of both reactions were the PET monomers of dimethyl terephthalate (DMT) and ethylene glycol (EG). The rate of PET depolymerization in supercritical methanol was faster than that of PET depolymerization in vapor methanol. This indicates supercritical fluid is beneficial in reducing reaction time without the use of a catalyst. We depicted the simple process flow of PET depolymerization in supercritical methanol and in vapor methanol, and by simulation evaluated the total heat demand of each process. In this simulation, bis-hydroxyethyl terephthalate (BHET) was used as a model component of PET. The total heat demand of PET depolymerization in supercritical methanol was 2.35 x 10(6)kJ/kmol Produced-DMT. That of PET depolymerization in vapor methanol was 2.84 x 10(6)kJ/kmol Produced-DMT. The smaller total heat demand of PET depolymerization in supercritical methanol clearly reveals the advantage of using supercritical fluid in terms of energy savings. PMID:16914302

  15. Supercritical methanol for polyethylene terephthalate depolymerization: Observation using simulator

    SciTech Connect

    Genta, Minoru; Iwaya, Tomoko; Sasaki, Mitsuru; Goto, Motonobu

    2007-07-01

    To apply PET depolymerization in supercritical methanol to commercial recycling, the benefits of supercritical methanol usage in PET depolymerization was investigated from the viewpoint of the reaction rate and energy demands. PET was depolymerized in a batch reactor at 573 K in supercritical methanol under 14.7 MPa and in vapor methanol under 0.98 MPa in our previous work. The main products of both reactions were the PET monomers of dimethyl terephthalate (DMT) and ethylene glycol (EG). The rate of PET depolymerization in supercritical methanol was faster than that of PET depolymerization in vapor methanol. This indicates supercritical fluid is beneficial in reducing reaction time without the use of a catalyst. We depicted the simple process flow of PET depolymerization in supercritical methanol and in vapor methanol, and by simulation evaluated the total heat demand of each process. In this simulation, bis-hydroxyethyl terephthalate (BHET) was used as a model component of PET. The total heat demand of PET depolymerization in supercritical methanol was 2.35 x 10{sup 6} kJ/kmol Produced-DMT. That of PET depolymerization in vapor methanol was 2.84 x 10{sup 6} kJ/kmol Produced-DMT. The smaller total heat demand of PET depolymerization in supercritical methanol clearly reveals the advantage of using supercritical fluid in terms of energy savings.

  16. Response to Comment on "A bacterium that degrades and assimilates poly(ethylene terephthalate)".

    PubMed

    Yoshida, Shosuke; Hiraga, Kazumi; Takehana, Toshihiko; Taniguchi, Ikuo; Yamaji, Hironao; Maeda, Yasuhito; Toyohara, Kiyotsuna; Miyamoto, Kenji; Kimura, Yoshiharu; Oda, Kohei

    2016-08-19

    Yang et al suggest that the use of low-crystallinity poly(ethylene terephthalate) (PET) exaggerates our results. However, the primary focus of our study was identifying an organism capable of the biological degradation and assimilation of PET, regardless of its crystallinity. We provide additional PET depolymerization data that further support several other lines of data showing PET assimilation by growing cells of Ideonella sakaiensis. PMID:27540160

  17. Controlled change of transport properties of poly(ethylene terephthalate) track membranes by plasma method

    NASA Astrophysics Data System (ADS)

    Kravets, L. I.; Dmitriev, S. N.; Drachev, A. I.; Gilman, A. B.; Lazea, A.; Dinescu, G.

    2007-04-01

    A process of plasma polymerization of dimethylaniline and acrylic acid vapours on the surface of poly(ethylene terephthalate) track membranes has been investigated. The surface and hydrodynamic properties of the composite membranes produced in this case have been studied. It is shown that the water permeability of the obtained polymeric membranes can be controlled by changing the filtrate pH. Membranes with such properties can be used for controllable drug delivery and in sensor control.

  18. [Determination of isophthalic acid in polyethylene glycol terephthalate fiber by high performance liquid chromatography].

    PubMed

    Wang, R; Wang, X Y; Tang, C J; Li, L P

    2001-07-01

    The isophthalic acid(IPA) is present in polyethylene glycol terephthalate(PET) at small level, but plays an important role for the properties of polyester fiber. Thus the PET sample was hydrolysated by 100 g/L of sodium hydrate in methanol at 70 degrees C during 10 h and finally assayed by HPLC. A reversed-phase high performance liquid chromatographic method for the separation of isophthalic acid from terephthalic acid(TPA) has been developed. The operating conditions were Novapak C18 column, methanol-water(15:85, V/V)(pH3) as mobile phase with the flow rate of 1.0 mL/min and UV detection wavelength at 254 nm. PMID:12545507

  19. Layered double hydroxide/polyethylene terephthalate nanocomposites. Influence of the intercalated LDH anion and the type of polymerization heating method

    SciTech Connect

    Herrero, M.; Martinez-Gallegos, S.; Labajos, F.M.; Rives, V.

    2011-11-15

    Conventional and microwave heating routes have been used to prepare PET-LDH (polyethylene terephthalate-layered double hydroxide) composites with 1-10 wt% LDH by in situ polymerization. To enhance the compatibility between PET and the LDH, terephthalate or dodecyl sulphate had been previously intercalated in the LDH. PXRD and TEM were used to detect the degree of dispersion of the filler and the type of the polymeric composites obtained, and FTIR spectroscopy confirmed that the polymerization process had taken place. The thermal stability of these composites, as studied by thermogravimetric analysis, was enhanced when the microwave heating method was applied. Dodecyl sulphate was more effective than terephthalate to exfoliate the samples, which only occurred for the terephthalate ones under microwave irradiation. - Graphical abstract: Conventional and microwave heating routes were used to prepare PET-LDH (polyethylene terephthalate-layered double hydroxide) composites with 1-10 wt% LDH by in situ polymerization. To enhance the compatibility between PET and the LDH, terephthalate or dodecyl sulphate was previously intercalated into the LDH. The microwave process improves the dispersion and the thermal stability of nanocomposites due to the interaction of the microwave radiation and the dipolar properties of EG and the homogeneous heating. Highlights: > LDH-PET compatibility is enhanced by preintercalation of organic anions. > Dodecylsulphate performance is much better than that of terephthalate. > Microwave heating improves the thermal stability of the composites. > Microwave heating improves as well the dispersion of the inorganic phase.

  20. Polymer adsorption on platinum: surface coverage determination using iodide-125. [Polyethylene glycol terephthalate

    SciTech Connect

    Ellis, T.M.; Van de Mark, M.R.; mi, FL

    1981-10-01

    Adsorption of iodide-125, a ..gamma.. emitter, was used as a quantitative methodology for polymer adsorption surface coverage analysis. Adsorption of I-125 on clean platinum produced surface elemental ratios of I:Pt of 1:4. The technique was applied to the adsorption of polyethylene glycol terephthalate from trifluoroacetic acid on platinum flags with a 2-cm/sup 2/ surface area. This polymer adsorption is approximated by a logarithmic relationship similar to the Temkin isotherm. Polymer coverage attained up to 99.6% of the surface.

  1. Poly(ethylene terephthalate) surface modification by deep UV (172 nm) irradiation

    SciTech Connect

    Zhengmao Zhua; Michael J. Kelley

    2004-09-01

    The prospects of obtaining desired surface-mediated characteristics while retaining bulk-mediated physical properties and avoiding potential environmental issues with wet chemical technology lends considerable appeal to photochemical approaches. We investigated the response of poly(ethylene terephthalate) to 172 nm UV from a xenon excimer lamp in the absence of oxygen, using XPS, ToF/SIMS, and AFM. The main effects are increasing loss of a C=O moiety and carboxylic acid production without effect on topography up to a total fluence of 16 J/cm2. Above this level no further change in surface chemistry was evident, but surfaces became rougher, suggesting the onset of etching.

  2. Morphological changes of poly(ethylene terephthalate) on multiple steam sterilization.

    PubMed

    Nair, P D

    1990-01-01

    Poly(ethylene terephthalate) (PET) was steam sterilized by autoclaving for 15, 30 and 60 min. The thermal properties, T m, delta-H and percent crystallinity were determined using differential scanning calorimetry. Molecular weight distribution was determined using gel permeation liquid chromatography. Crystallinity of PET was also monitored by infrared spectrophotometry. The analyses indicate that that chain scission and cyclization reactions take place in PET, forming cyclic oligomers, that can migrate to the polymer surface and which may affect long term performance of PET. PMID:10150080

  3. Molecular dynamics of poly(ethylene terephthalate)/poly(phenylene sulfide) nanocomposites with barium titanate

    NASA Astrophysics Data System (ADS)

    Konieczna, Monika; Woźniak-Braszak, Aneta; Hołderna-Natkaniec, Krystyna; Jurga, Jan

    2011-04-01

    The relaxation processes and the properties of polymer/ceramic nanocomposites have been studied by the 1H nuclear magnetic resonance methods. Nanocomposites of poly(ethylene terephthalate) PET and poly(phenylene sulfide) PPS with 0.25, 2.5 and 5% wt. barium titanate BT were prepared using a twin screw extruder and injection moulding machine. The spin-lattice relaxation time T1, second moment M2 and the motional parameters as e.g. the activation energies in the nanocomposites were investigated.

  4. Effects of ionizing radiation on the viscoelasticity of glassy polyethylene terephthalate films

    NASA Astrophysics Data System (ADS)

    Shaban, A. M.; El-Tonsy, M. M.; Kinawy, N.

    1995-03-01

    The viscoelastic properties of Gamma-ray irradiated polyethylene terephthalate (PET) sheets, extruded in the glassy state, were measured by a method of forced resonance oscillations. Density variations due to ?-irradiation with different doses were found suitable to describe changes of the cross-linking rate. The dynamic Young's modulus of PET-films showed a decrease within the dose range 200-500 kGy which has anomalous behaviour related to the glass transition (alpha-relaxation) by ?-irradiation to a rubberlike state at a dose of 200 kGy. The low frequency velocity of sound showed no correlation with the density of irradiated PET-films.

  5. Flexible metal-insulator-metal capacitors on polyethylene terephthalate plastic substrates

    NASA Astrophysics Data System (ADS)

    Hota, M. K.; Bera, M. K.; Maiti, C. K.

    2012-10-01

    Realization of flexible electronic devices on polyethylene terephthalate flexible plastic substrates is reported. Metal-insulator-metal capacitors have been fabricated using radio frequency sputtered deposited thin films of Nb2O5 on the flexible substrate. Good electrical characteristics have been obtained in terms of quadratic voltage coefficient of capacitance, high capacitance density (˜ 11 fF µm-2), high dielectric constant (˜37) and low dissipation factor (<0.1). Besides, in repetitive bending test, the devices show excellent electrical stability and high mechanical flexibility due to the high ductility of niobium and low-temperature processing used in this study.

  6. Migration into food of polyethylene terephthalate (PET) cyclic oligomers from PET microwave susceptor packaging.

    PubMed

    Begley, T H; Dennison, J L; Hollifield, H C

    1990-01-01

    A quantitative method has been developed to measure the migration of polyethylene terephthalate (PET) cyclic oligomers from aluminized PET susceptor film-type food packaging into several food types. Microwaveable French fries, popcorn, fish sticks, waffles and pizza sold in susceptor-type packaging were purchased in local markets, cooked according to package instructions and analysed for PET oligomers. Appropriate food blanks were cooked in glass containers. Quantities of PET oligomers found in the foods ranged from less than 0.012 micrograms/g to approximately 7 micrograms/g. PMID:2150379

  7. Wood plastic composites based on microfibrillar blends of high density polyethylene/poly(ethylene terephthalate).

    PubMed

    Lei, Yong; Wu, Qinglin

    2010-05-01

    High-melting-temperature poly(ethylene terephthalate) (PET) was successfully introduced into wood plastic composites through a two-step reactive extrusion technology. Wood flour was added into pre-prepared PET/high density polyethylene (HDPE) microfibrillar blends (MFBs) in the second extrusion at the temperature for processing HDPE. Addition of 25% in situ formed PET microfibers obviously increased the mechanical properties of HDPE, and more significant enhancement by the in situ formed recycled PET microfibers was observed for the recycled HDPE. Adding 2% E-GMA improved the compatibility between matrix and microfibers in MFBs, resulting further enhanced mechanical properties. The subsequent addition of 40% wood flour did not influence the size and morphology of PET microfibers, and improved the comprehensive mechanical properties of MFBs. The wood flour increased the crystallinity level of HDPE in the compatibilized MFB in which PET phase did not crystallize. The storage modulus of MFB was greatly improved by wood flour. PMID:20100654

  8. Engineered bacterial polyester hydrolases efficiently degrade polyethylene terephthalate due to relieved product inhibition.

    PubMed

    Wei, Ren; Oeser, Thorsten; Schmidt, Juliane; Meier, René; Barth, Markus; Then, Johannes; Zimmermann, Wolfgang

    2016-08-01

    Recent studies on the enzymatic degradation of synthetic polyesters have shown the potential of polyester hydrolases from thermophilic actinomycetes for modifying or degrading polyethylene terephthalate (PET). TfCut2 from Thermobifida fusca KW3 and LC-cutinase (LCC) isolated from a compost metagenome are remarkably active polyester hydrolases with high sequence and structural similarity. Both enzymes exhibit an exposed active site in a substrate binding groove located at the protein surface. By exchanging selected amino acid residues of TfCut2 involved in substrate binding with those present in LCC, enzyme variants with increased PET hydrolytic activity at 65°C were obtained. The highest activity in hydrolyzing PET films and fibers were detected with the single variant G62A and the double variant G62A/I213S. Both variants caused a weight loss of PET films of more than 42% after 50 h of hydrolysis, corresponding to a 2.7-fold increase compared to the wild type enzyme. Kinetic analysis based on the released PET hydrolysis products confirmed the superior hydrolytic activity of G62A with a fourfold higher hydrolysis rate constant and a 1.5-fold lower substrate binding constant than those of the wild type enzyme. Mono-(2-hydroxyethyl) terephthalate is a strong inhibitor of TfCut2. A determination of the Rosetta binding energy suggested a reduced interaction of G62A with 2PET, a dimer of the PET monomer ethylene terephthalate. Indeed, G62A revealed a 5.5-fold lower binding constant to the inhibitor than the wild type enzyme indicating that its increased PET hydrolysis activity is the result of a relieved product inhibition by mono-(2-hydroxyethyl) terephthalate. Biotechnol. Bioeng. 2016;113: 1658-1665. © 2016 Wiley Periodicals, Inc. PMID:26804057

  9. 75 FR 9579 - Polyethylene Terephthalate Film, Sheet, and Strip from the Republic of Korea: Extension of Time...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-03

    ... Antidumping and Countervailing Duty Administrative Reviews and Deferral of Administrative Review, 74 FR 39690... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip from the Republic of Korea... additional time to gather and analyze information relating to Kolon's cost of production, home market...

  10. 76 FR 4288 - Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea: Extension of Time...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-25

    ... Antidumping and Countervailing Duty Administrative Reviews and Requests for Revocation in Part, 75 FR 44224... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea... because we require additional time to collect and analyze information regarding costs of production...

  11. 77 FR 18206 - Polyethylene Terephthalate Film, Sheet, and Strip (PET Film) From Taiwan: Extension of Time Limit...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-27

    ... Duty Administrative Reviews and Requests for Revocation in Part, 76 FR 53404 (August 26, 2011). This... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip (PET Film) From Taiwan... Department) initiated the administrative review regarding the antidumping duty order on PET Film from...

  12. 77 FR 20357 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates: Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-04-04

    ... Antidumping Duties, 68 FR 23954 (May 6, 2003). \\4\\ See id.; see also Polyethylene Terephthalate Film, Sheet... Administrative Review, 76 FR 76365 (December 7, 2011). DATES: Effective Date: April 4, 2012 FOR FURTHER... FR 66595 (November 10, 2008) (Order). Cash Deposit Requirements The following deposit...

  13. 75 FR 70901 - Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea: Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-11-19

    ... Antidumping Duty Administrative Review, 75 FR 40784 (July 14, 2010) (Preliminary Results). This review covers... Court Decision and Amended Final Determination of Antidumping Duty Investigation, 62 FR 50557 (September... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of...

  14. 78 FR 14266 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Notice of Correction to the Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-03-05

    ... Results of Antidumping Duty Administrative Review; 2010-2011, 78 FR 9668 (February 11, 2013) (Final Results). \\2\\ Id. 78 FR at 9668. This correction is published in accordance with sections 751(h) and 777(i... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Notice...

  15. Glass transition dynamics and cooperativity length of poly(ethylene 2,5-furandicarboxylate) compared to poly(ethylene terephthalate).

    PubMed

    Codou, Amandine; Moncel, Matthieu; van Berkel, Jesper Gabriël; Guigo, Nathanaël; Sbirrazzuoli, Nicolas

    2016-06-22

    The glass transition of poly(ethylene 2,5-furandicarboxylate) (PEF), an emergent bio-based polyester, was investigated in comparison to one of its chemical analogues: poly(ethylene terephthalate) (PET). These investigations were conducted at different crystallinities by means of stochastic modulated differential scanning calorimetry (stochastic TMDSC) and dynamic mechanical analysis (DMA). Amorphous PEF presents a higher ΔCp at the glass transition and a broader relaxation spectrum attributed to a higher free volume. The higher Tg of PEF is then purely related to segmental mobility and specific interactions in PEF. The length of cooperative rearranging regions (CRR) was similar for both materials. Additionally, the variations of the effective activation energy E of PEF and PET at glass transitions were determined by isoconversional kinetic analysis. The rate of decrease in E was similar for the two amorphous polyesters. Upon crystallization, the glass transition of PEF is broadened but its temperature range is not increased as with PET. The creation of the rigid amorphous fraction (RAF) with crystallinity is lower in PEF than in PET. The difference in free volume also explains the lower coupling between the crystalline phase and the amorphous phase in PEF. PMID:27067510

  16. Effect of calcium-ozone treatment on chemical and biological properties of polyethylene terephthalate.

    PubMed

    Rashid, Ahmed Nafis; Tsuru, Kanji; Ishikawa, Kunio

    2015-05-01

    Ozone (O3 ) treatment of polyethylene terephthalate (PET) in distilled water was performed in the presence and absence of calcium (Ca(2+) ). PET was oxidized and thus carboxylic and hydroxyl functional groups were introduced on its surface after O3 treatment, regardless of the presence or absence of Ca(2+) . In the case of O3 treatment with Ca(2+) , PET surface was modified with Ca(2+) . Ca(2+) immobilization was confirmed by X-ray photoelectron spectrometric analysis. Hydrophilicity was investigated by measuring contact angles (CA). CA of PET decreased significantly after ozonation. Surface topography of PET before and after ozone treatment was observed by scanning electron microscopy, and showed no morphological changes. In vitro studies showed enhanced rat bone marrow cell responses on the O3 -treated PET surface. Ca(2+) -O3 oxidation at 37°C for 6 h is expected to be an effective method to fabricate PET with good biocompatibility. PMID:25137565

  17. Plasma sterilization of polyethylene terephthalate bottles by pulsed corona discharge at atmospheric pressure.

    PubMed

    Masaoka, Satoshi

    2007-06-01

    A pulsed power supply was used to generate a corona discharge on a polyethylene terephthalate bottle, to conduct plasma sterilization at atmospheric pressure. Before generating such a discharge, minute quantities of water were attached to the inner surface of the bottle and to the surface of a high voltage (HV) electrode inserted into the bottle. Next, high-voltage pulses of electricity were discharged between electrodes for 6.0s, while rotating the bottle. The resulting spore log reduction values of Bacillus subtilis and Aspergillus niger on the inner surface of the bottle were 5.5 and 6 or higher, respectively, and those on the HV electrode surface were each 6 or higher for both strains. The presence of the by-products gaseous ozone, hydrogen peroxide, and nitric ions resulting from the electrical discharge was confirmed. PMID:17629247

  18. Modification of polyethylene terephthalate under high-energy heavy ion irradiation

    NASA Astrophysics Data System (ADS)

    Zhu, Zhiyong; Liu, Changlong; Sun, Youmei; Liu, Jie; Tang, Yuhua; Jin, Yunfan; Du, Junli

    2002-05-01

    Polyethylene terephthalate films were irradiated with high-energy heavy ions to fluences ranging from 9×10 9 to 5.5×10 12 ions/cm 2. The radiation-induced changes in molecular and crystalline structures were investigated by the Fourier-transform infrared (FTIR) spectroscopy and the X-ray diffraction measurement. FTIR spectra measurements reveal that the material suffers serious degradation through bond breaking. The absorbance of the typical infrared bands decays exponentially with increase of ion fluence and the bond-disruption cross-section shows a sigmoid variation with the electronic energy loss. The semi-crystalline structure of the material is destroyed by the irradiation with processes that are electronic energy loss dependent. At lower electronic energy loss values the amorphization is closely related to the destruction of the trans-configuration of the ethylene glycol residue. At high electronic energy loss, however, other processes determine the amorphization.

  19. Growth and optical properties of Ag clusters deposited on poly(ethylene terephthalate).

    PubMed

    Flores-Camacho, J M; Weidlinger, G; Sun, L D; Schmidegg, K; Hohage, M; Primetzhofer, D; Bauer, P; Zeppenfeld, P

    2011-07-01

    The growth and concomitant evolution of the optical properties of Ag nano-clusters deposited on biaxially extruded poly(ethylene terephthalate) films is studied by reflectance difference spectroscopy. It is demonstrated by low energy ion scattering and simulated optical spectra that the clusters form a two-dimensional layer buried beneath the surface of the substrate. The experimental spectra are described by simulations in which different configurations of the host such as anisotropy, amorphization, and dilution are considered in an effective medium approach. The contribution of the anisotropic substrate is used to explain the resulting line shapes. We also discuss the role of the rate of change of the filling fraction with Ag coverage in the evolution of the spectra and the detection of the onset of coalescence by optical means. PMID:21597154

  20. Determination of the detection threshold for Polyethylene Terephthalate (PET) Nuclear Track Detector (NTD)

    NASA Astrophysics Data System (ADS)

    Bhattacharyya, R.; Dey, S.; Ghosh, Sanjay K.; Maulik, A.; Raha, Sibaji; Syam, D.

    2016-03-01

    In this work we investigated the detection threshold of the polymer material Polyethylene Terephthalate (PET) intended to be used as Nuclear Track Detector (NTD) in the search for rare events (e.g. strangelets) in cosmic rays. 11 MeV 12C and 2 MeV proton beams from the accelerator at the Institute of Physics (IOP), Bhubaneswar were utilized for this study. The results show that the PET detector has a much higher detection threshold (Z / β ∼ 140) compared to many other commercially available and widely used detector materials like CR-39 (Z / β ∼ 6-20) or Makrofol (Z / β ∼ 57). This makes PET a particularly suitable detector material for testing certain phenomenological models which predict the presence of strangelets as low energy, heavily ionizing particles in cosmic radiation at high mountain altitudes.

  1. Ion track symmetric and asymmetric nanopores in polyethylene terephthalate foils for versatile applications

    NASA Astrophysics Data System (ADS)

    Apel, P. Yu.; Blonskaya, I. V.; Dmitriev, S. N.; Orelovich, O. L.; Sartowska, B. A.

    2015-12-01

    In this report we present several fabrication methods which allow production of ion track nanopore membranes with different pore configurations. Polymer foils, typically polyethylene terephthalate with a thickness of 5-23 μm, are irradiated with accelerated heavy ions (energy of 1-10 MeV/u) and then subjected to different physico-chemical treatments. Depending on the procedure, symmetric or asymmetric pores with nanoscale-sized narrowing are obtained. The asymmetric configurations include conical, funnel-like and bullet-like shapes. In electrolyte solutions the asymmetric nanopores exhibit diode-like properties which strongly depend on the pore shape. The peculiar features of such pores provide a basis for various applications.

  2. Bendable ZnO thin film surface acoustic wave devices on polyethylene terephthalate substrate

    SciTech Connect

    He, Xingli; Guo, Hongwei; Chen, Jinkai; Wang, Wenbo; Xuan, Weipeng; Xu, Yang E-mail: jl2@bolton.ac.uk; Luo, Jikui E-mail: jl2@bolton.ac.uk

    2014-05-26

    Bendable surface acoustic wave (SAW) devices were fabricated using high quality c-axis orientation ZnO films deposited on flexible polyethylene terephthalate substrates at 120 °C. Dual resonance modes, namely, the zero order pseudo asymmetric (A{sub 0}) and symmetric (S{sub 0}) Lamb wave modes, have been obtained from the SAW devices. The SAW devices perform well even after repeated flexion up to 2500 με for 100 times, demonstrating its suitability for flexible electronics application. The SAW devices are also highly sensitive to compressive and tensile strains, exhibiting excellent anti-strain deterioration property, thus, they are particularly suitable for sensing large strains.

  3. Non-isothermal melt crystallization behavior of Poly(ethylene terephthalate)/graphene nanocomposites

    NASA Astrophysics Data System (ADS)

    Aoyama, Shigeru; Park, Yong Tae; Ougizawa, Toshiaki; Macosko, Christopher

    2013-03-01

    Poly(ethylene terephthalate)(PET)/graphene nanocomposites were prepared by melt mixing with a goal of reduced gas permeability. With 2 wt% of few layered graphene, PET/graphene composite films show more than 70% decrease in N2 gas permeation. Their non-isothermal crystallization were also investigated by differential scanning calorimetory (DSC). Crystallization temperature, Tc, of PET/graphene nanocomposites was more than 8 °C higher than neat PET and the increment increased along with the concentration of graphene. This suggests that the nucleation effect of graphene enhanced with the increase in concentration of graphene. On the other hand, PET/graphene nanocomposites show shorter half crystallization time, t1/2, than neat PET at lower concentrations, but t1/2 increased along with concentration of graphene. From Raman spectroscopy, it was shown that PET chains in nanocomposites are strongly confined in the presence of an excess of graphene. Restricted mobility of PET chains slowed crystallization.

  4. Positron annihilation lifetime spectroscopy of poly(ethylene terephthalate): Contributions from rigid and mobile amorphous fractions

    NASA Astrophysics Data System (ADS)

    Olson, Brian; Lin, Jun; Nazarenko, Sergei; Jamieson, Alexander

    2004-03-01

    Systematic divergences in the orthopositronium (o-Ps) annihilation lifetimes, τ_3, and intensities, I_3, are observed, when comparing melt-crystallized and cold-crystallized poly(ethylene terephthalate) (PET) as a function of crystallinity. Following a previous analysis of corresponding deviations in oxygen permeability, the divergences in I3 and τ3 are traced to distinct characteristic values for the probability of o-Ps formation and o-Ps lifetime in the rigid amorphous phase (RAF) associated with the crystalline lamellae and the mobile amorphous regions (MAF) which are unperturbed by the presence of the crystal phase. Utilizing independent information on the volume fractions of RAF and MAF, a quantitative analysis of the o-Ps annihilation parameters is possible.

  5. High impact strength polyethylene terephthalate (PET) from virgin and recycled resins

    SciTech Connect

    Abu-Isa, I.A.; Jaynes, C.B.; O`Gara, J.F.

    1995-12-31

    The impact strength of polyethylene terephthalate (PET) have been dramatically improved by blending with a copolyester thermoplastic elastomer, or an acrylate core/shell elastomer. The addition of triphenyl phosphite (TPP) to the polyester elastomer/PET blends, encouraged molecular weight buildup and resulted in improved impact strength and tensile properties. Up to 60 fold increase in impact strength of PET was obtained by blending with elastomers in the presence of TPP. It was suspected that the phosphite interacts chemically with the components of the blend during processing and produces the improvements. Phosphorus-31 ({sup 31}P) NMR techniques have provided a direct spectroscopic probe of the chemical nature of the phosphite additive after the processing steps. Solution and solid state spectra have revealed the presence of products in which the polymer chains are grafted and cross-linked through the phosphorus additive.

  6. Surface modification of poly(ethylene terephthalate) fibers induced by radio frequency air plasma treatment

    NASA Astrophysics Data System (ADS)

    Riccardi, Claudia; Barni, Ruggero; Selli, Elena; Mazzone, Giovanni; Massafra, Maria Rosaria; Marcandalli, Bruno; Poletti, Giulio

    2003-04-01

    The surface chemical and physical modifications of poly(ethylene terephthalate) (PET) fibers induced by radiofrequency air plasma treatments were correlated with the characteristics of the discharge parameters and the chemical composition of the plasma itself, to identify the plasma-induced surface processes prevailing under different operating conditions. Treated polymer surfaces were characterized by water droplet absorption time measurements and XPS analysis, as a function of the aging time in different media, and by AFM analysis. They exhibited a remarkable increase in hydrophilicity, accompanied by extensive etching and by the implantation of both oxygen- and nitrogen-containing polar groups. Etching was mainly a consequence of ion bombardment, yielding low molecular weight, water soluble oxidation products, while surface chemical modifications were mainly due to the action of neutral species on the plasma-activated polymer surface.

  7. Polyethylene terephthalate/poly(vinylidene fluoride) composite separator for Li-ion battery

    NASA Astrophysics Data System (ADS)

    Wu, Dezhi; Huang, Shaohua; Xu, Zhiqin; Xiao, Zhiming; Shi, Chuan; Zhao, Jinbao; Zhu, Rui; Sun, Daoheng; Lin, Liwei

    2015-06-01

    Electrospun nanofiber membranes have been proved to enhance the performance of a Li-ion battery (LIB), but their poor mechanical strength hinders their industrial application. This paper combines a meltblown polyethylene terephthalate (PET) nonwoven and a electrospun poly(vinylidene fluoride) (PVDF) membrane together to improve the mechanical property via hot-pressing, wherein a dried 3 wt% PVDF solution coating on PET nonwoven is used as a binder. The experiment results indicate that the hot-pressing PET/PVDF separator exhibits an excellent mechanical property, whose transverse and longitudinal tensile strength could reach 13.70 MPa and 34.85 MPa respectively. Compared with a commercial PP separator, the hot-pressing PET/PVDF membrane separator shows better wettability, higher thermal shrinkage and excellent discharge capacity as well.

  8. Polyethylene terephthalate/poly (vinylidene fluoride) composite separator for Li-ion battery

    NASA Astrophysics Data System (ADS)

    Wu, Dezhi; Huang, Shaohua; Xu, Zhiqin; Xiao, Zhiming; Shi, Chuan; Zhao, Jinbao; Zhu, Rui; Sun, Daoheng; Lin, Liwei

    2015-07-01

    Electrospun nanofiber membranes have been proved to enhance performances of Li-ion batteries, but their poor mechanical strength hinders their industrial application. This paper combines meltblown polyethylene terephthalate (PET) nonwoven and electrospun poly (vinylidene fluoride) (PVDF) membrane together to improve the mechanical property via hot-pressing, wherein a dried 3 wt% PVDF solution coating on PET nonwoven is used as a binder. The hot-pressing temperature is optimized to be 145 °C and the composite PET/PVDF separator exhibits an excellent mechanical property, whose transverse and longitudinal tensile strength could reach 13.70 and 34.85 MPa respectively. Compared with a commercial PP separator, the hot-pressed PET/PVDF membrane separator shows better wettability, higher thermal shrinkage and improved electrochemical performance as well.

  9. Preparation and characterization of nonfouling polymer brushes on poly(ethylene terephthalate) film surfaces.

    PubMed

    Li, Jiehua; Tan, Dongsheng; Zhang, Xiaoqing; Tan, Hong; Ding, Mingming; Wan, Changxiu; Fu, Qiang

    2010-07-01

    In this study, a surface grafting of nonfouling poly(ethylene glycol) methyl ether acrylate (PEGMA) on poly(ethylene terephthalate) (PET) was carried out via surface-initiated atom-transfer radical polymerization (SI-ATRP) to improve hemocompatibility of polymer based biomaterials. To do this, the coupling agent with hydroxyl groups for the ATRP initiator was first anchored on the surface of PET films using photochemical method, and then these hydroxyl groups were esterified by bromoisobutyryl bromide, from which PET with various main chain lengths of PEGMA was prepared. The structures and properties of modified PET surfaces were investigated using water contact angle (WAC), ATR-FTIR, X-ray photoelectron spectroscopy (XPS) and Atomic force microscopy (AFM). The molecular weights of the free polymer from solution were determined by gel permeation chromatography (GPC). These results indicated that grafting of PEGMA on PET film is a simple way to change its surface properties. The protein adsorption resistance on the surfaces of PET was primarily evaluated by an enzyme-linked immunosorbent assay (ELISA). The result demonstrated that the protein adsorption could be well suppressed by poly(PEGMA) brush structure on the surface of PET. This work provides a new approach for polymers to enhance their biocompatibility. PMID:20399623

  10. Enhanced Cutinase-Catalyzed Hydrolysis of Polyethylene Terephthalate by Covalent Fusion to Hydrophobins

    PubMed Central

    Ribitsch, Doris; Herrero Acero, Enrique; Przylucka, Agnieszka; Zitzenbacher, Sabine; Marold, Annemarie; Gamerith, Caroline; Tscheließnig, Rupert; Jungbauer, Alois; Rennhofer, Harald; Lichtenegger, Helga; Amenitsch, Heinz; Bonazza, Klaus; Kubicek, Christian P.; Guebitz, Georg M.

    2015-01-01

    Cutinases have shown potential for hydrolysis of the recalcitrant synthetic polymer polyethylene terephthalate (PET). We have shown previously that the rate of this hydrolysis can be enhanced by the addition of hydrophobins, small fungal proteins that can alter the physicochemical properties of surfaces. Here we have investigated whether the PET-hydrolyzing activity of a bacterial cutinase from Thermobifida cellulosilytica (Thc_Cut1) would be further enhanced by fusion to one of three Trichoderma hydrophobins, i.e., the class II hydrophobins HFB4 and HFB7 and the pseudo-class I hydrophobin HFB9b. The fusion enzymes exhibited decreased kcat values on soluble substrates (p-nitrophenyl acetate and p-nitrophenyl butyrate) and strongly decreased the hydrophilicity of glass but caused only small changes in the hydrophobicity of PET. When the enzyme was fused to HFB4 or HFB7, the hydrolysis of PET was enhanced >16-fold over the level with the free enzyme, while a mixture of the enzyme and the hydrophobins led only to a 4-fold increase at most. Fusion with the non-class II hydrophobin HFB9b did not increase the rate of hydrolysis over that of the enzyme-hydrophobin mixture, but HFB9b performed best when PET was preincubated with the hydrophobins before enzyme treatment. The pattern of hydrolysis by the fusion enzymes differed from that of Thc_Cut1 as the concentration of the product mono(2-hydroxyethyl) terephthalate relative to that of the main product, terephthalic acid, increased. Small-angle X-ray scattering (SAXS) analysis revealed an increased scattering contrast of the fusion proteins over that of the free proteins, suggesting a change in conformation or enhanced protein aggregation. Our data show that the level of hydrolysis of PET by cutinase can be significantly increased by fusion to hydrophobins. The data further suggest that this likely involves binding of the hydrophobins to the cutinase and changes in the conformation of its active center. PMID:25795674

  11. Fabrication of two dimensional polyethylene terephthalate nanofluidic chip using hot embossing and thermal bonding technique

    PubMed Central

    Yin, Zhifu; Zou, Helin; Chen, Li; Xu, Shenbo

    2014-01-01

    We present in this paper a method for obtaining a low cost and high replication precision 2D (two dimensional) nanofluidic chip with a PET (polyethylene terephthalate) sheet, which uses hot embossing and a thermal bonding technique. The hot embossing process parameters were optimized by both experiments and the finite element method to improve the replication precision of the 2D nanochannels. With the optimized process parameters, 174.67 ± 4.51 nm wide and 179.00 ± 4.00 nm deep nanochannels were successfully replicated into the PET sheet with high replication precision of 98.4%. O2 plasma treatment was carried out before the bonding process to decrease the dimension loss and improve the bonding strength of the 2D nanofluidic chip. The bonding parameters were optimized by bonding rate of the nanofluidic chip. The experiment results show that the bonding strength of the 2D PET nanofluidic chip is 0.664 MPa, and the total dimension loss of 2D nanochannels is 4.34 ± 7.03 nm and 18.33 ± 9.52 nm, in width and depth, respectively. The fluorescence images demonstrate that there is no blocking or leakage over the entire micro- and nanochannels. With this fabrication technology, low cost polymer nanochannels can be fabricated, which allows for commercial manufacturing of nano-components. PMID:25553203

  12. Physical ageing of polyethylene terephthalate under natural sunlight: correlation study between crystallinity and mechanical properties

    NASA Astrophysics Data System (ADS)

    Aljoumaa, Khaled; Abboudi, Maher

    2016-01-01

    Semi-crystalline polyethylene terephthalate (PET) was aged under the effect of natural UV exposure and outdoor temperature during 670 days. The variation in the mechanical and thermal properties beside to the morphology was tracked by applying different analytical techniques, including scanning electron microscopy, infrared spectroscopy, differential scanning calorimetry and wide angle X-ray diffraction, in addition to tensile strength and hardness measurements. It has been confirmed that the ageing process is the results of physical trend only. The aged PET showed a decrease in both tensile strength and strain with an increase in the degree of crystallinity of aged PET samples during the whole period. These changes in crystallinity were examined by various analysis methods: density, calorimetric and infrared spectroscopy. New peaks in FTIR analysis at 1115 and 1090 cm-1 were characterized and proved that this technique is considered to be an easy tool to track the change in the surface crystallinity of aged PET samples directly. The results of this study showed that an augmentation in the degree of crystallinity of outdoor aged PET samples from 18 to 36 %, accompanied with a decrease in tensile strength from 167.9 to 133.7 MPa. Moreover, a good exponential correlation was found between the degree of crystallinity and the mechanical properties of the aged PET.

  13. Leaching of antimony from polyethylene terephthalate (PET) bottles into mineral water.

    PubMed

    Keresztes, Szilvia; Tatár, Eniko; Mihucz, Victor G; Virág, István; Majdik, Cornelia; Záray, Gyula

    2009-08-01

    The Sb leaching from polyethylene terephthalate (PET) package material into 10 different brands of still (non-carbonated) and sparkling (carbonated) Hungarian mineral water purchased in supermarkets was investigated by inductively coupled plasma sector field mass spectrometry (ICP-SF-MS). The Sb concentration measured in PET package materials varied between 210 and 290 mg/kg. Generally, the Sb concentration of still mineral water was lower than that of sparkling in the case of identical storage time. For modelling improper storage conditions, storage time (10-950 days), temperature (22 degrees C-70 degrees C), illumination (dark vs. 23 W daylight lamp for 116 h) as well as bottle volume (0.5, 1.0 and 1.5 L) were taken into consideration. Under certain extreme light and temperature storage conditions, the Sb concentration of some samples exceeded the concentration value of 2 ng/mL. The extent of Sb leaching from the PET recipients of different brands of mineral water can differ by even one order of magnitude in experiments conducted under the same conditions. Thus, the adequate selection of the polymer used for the production of the PET bottle for the solar water disinfection (SODIS) procedure seems to ensure low Sb levels in the water samples. PMID:19467696

  14. Atmospheric pressure synthesis of photoluminescent hybrid materials by sequential organometallic vapor infiltration into polyethylene terephthalate fibers

    SciTech Connect

    Akyildiz, Halil I.; Mousa, Moataz Bellah M.; Jur, Jesse S.

    2015-01-28

    Exposing a polymer to sequential organometallic vapor infiltration (SVI) under low pressure conditions can significantly modify the polymer's chemical, mechanical, and optical properties. We demonstrate that SVI of trimethylaluminum into polyethylene terephthalate (PET) can also proceed readily at atmospheric pressure, and at 60 °C the extent of reaction determined by mass uptake is independent of pressure between 2.5 Torr and 760 Torr. At 120 °C, however, the mass gain is 50% larger at 2.5 Torr relative to that at 760 Torr, indicating that the precursor diffusion in the chamber and fiber matrix decreases at higher source pressure. Mass gain decreases, in general, as the SVI process temperature increases both at 2.5 Torr and 760 Torr attributed to the faster reaction kinetics forming a barrier layer, which prevents further diffusion of the reactive species. The resulting PET/Al-O{sub x} product shows high photoluminescence compared to untreated fibers. A physical mask on the polymer during infiltration at 760 Torr is replicated in the underlying polymer, producing an image in the polymer that is visible under UV illumination. Because of the reduced precursor diffusivity during exposure at 760 Torr, the image shows improved resolution compared to SVI performed under typical 2.5 Torr conditions.

  15. Flotation separation of polyvinyl chloride and polyethylene terephthalate plastics combined with surface modification for recycling.

    PubMed

    Wang, Chongqing; Wang, Hui; Fu, Jiangang; Zhang, Lingling; Luo, Chengcheng; Liu, Younian

    2015-11-01

    Surface modification with potassium permanganate (KMnO4) solution was developed for separation of polyvinyl chloride (PVC) and polyethylene terephthalate (PET) waste plastics. The floatability of PVC decreases with increasing of KMnO4 concentration, treatment time, temperature and stirring rate, while that of PET is unaffected. Fourier transform infrared (FT-IR) analysis confirms that mechanism of surface modification may be due to oxidization reactions occurred on PVC surface. The optimum conditions are KMnO4 concentration 1.25 mM/L, treatment time 50 min, temperature 60°C, stirring rate 300 r/min, frother concentration 17.5 g/L and flotation time 1 min. PVC and PET with different particle sizes were separated efficiently through two-stage flotation. Additionally, after ultrasonic assisted surface modification, separation of PVC and PET with different mass ratios was obtained efficiently through one-stage flotation. The purity and the recovery of the obtained products after flotation separation are up to 99.30% and 99.73%, respectively. A flotation process was designed for flotation separation of PVC and PET plastics combined with surface modification. This study provides technical insights into physical separation of plastic wastes for recycling industry. PMID:26253330

  16. Elasticity and photoelasticity relationships for polyethylene terephthalate fiber networks by molecular simulation.

    PubMed

    Nayak, Kapileswar; Das, Sushanta; Nanavati, Hemant

    2008-01-01

    We present a framework for the development of elasticity and photoelasticity relationships for polyethylene terephthalate fiber networks, incorporating aspects of the primary molecular structure. Semicrystalline polymeric fiber networks are modeled as sequentially arranged crystalline and amorphous regions. Rotational isomeric states-Monte Carlo simulations of amorphous chains of up to 360 bonds (degree of polymerization, DP=60), confined between and bridging infinite impenetrable crystalline walls, have been characterized by Omega, the probability density of the intercrystal separation h, and Deltabeta, the polarizability anisotropy. ln Omega and Deltabeta have been modeled as functions of h, yielding the chain deformation relationships. The development has been extended to the fiber network to yield the photoelasticity relationships. We execute our framework by fitting to experimental stress-elongation data and employing the single fitted parameter to directly predict the birefringence-elongation behavior, without any further fitting. Incorporating the effect of strain-induced crystallization into the framework makes it physically more meaningful and yields accurate predictions of the birefringence-elongation behavior. PMID:18190221

  17. Crystallization processes in poly(ethylene terephthalate) as modified by polymer additives and fiber reinforcement

    SciTech Connect

    Reinsch, V.E.; Rebenfeld, L.

    1993-12-31

    The effect of fiber reinforcement on the crystallization of poly(ethylene terephthalate) (PET) was investigated using differential scanning calorimetry. The objective of the study was to determine how the effects of fiber reinforcement on PET crystallization are modified by the presence of polymer additives. The interaction of fiber effects and nucleating and plasticizing agents was studied. Unidirectional fiber composites were prepared using aramid and glass fibers in PET. The rate of crystallization of PET, as reflected by crystallization half-time, it seem to depend on reinforcing fiber type, crystallization temperature, and presence of nucleant or plasticizer. However, degree of crytallinity of PET is largely unaffected by the presence of additives and reinforcing fibers. Crystallization kinetics are analyzed using a series Avrami model for PET volume crystallized as a function of time. The using a series Arami model for PET volume crystallized as a function of time. The crystalline morphology of fiber reinforced PET was studied using polarized light microscopy. Results concerning nucleation density, chain mobility, and growth morphology are used in explaining differences seen in crystallization kinetics in fiber reinforced systems.

  18. Patterning of Aluminium thin film on polyethylene terephthalate by multi-beam picosecond laser

    NASA Astrophysics Data System (ADS)

    Jin, Y.; Perrie, W.; Harris, P.; Allegre, O. J.; Abrams, K. J.; Dearden, G.

    2015-11-01

    High speed patterning of a 30 nm thick Aluminium thin film on a flexible Polyethylene Terephthalate substrate was demonstrated with the aid of Computer Generated Holograms (CGH's) applied to a phase only Spatial Light Modulator. Low fluence picosecond laser pulses minimise thermal damage to the sensitive substrate and thus clean, single and multi-beam, front side thin film removal is achieved with good edge quality. Interestingly, rear side ablation shows significant Al film delamination. Measured front and rear side ablation thresholds were Fth=0.20±0.01 J cm-2 and Fth=0.15±0.01 J cm-2 respectively. With laser repetition rate of 200 kHz and 8 diffractive spots, a film removal rate of R>0.5 cm2 s-1 was demonstrated during patterning with a fixed CGH and 5 W average laser power. The effective laser repetition rate was feff~1.3 MHz. The application of 30 stored CGH's switching up to 10 Hz was also synchronised with motion control, allowing dynamic large area multi-beam patterning which however, slows micro-fabrication.

  19. Enhanced UV-assisted vertical etching of polyethylene terephthalate for fabrication of microsystems

    NASA Astrophysics Data System (ADS)

    Jahanshahi, A.; Pajouhi, H.; Tamaddon, A. H.; Sadeghi, A.; Mohajerzadeh, S.; Khadem-Hoseiny, B.

    2009-07-01

    The improved ultraviolet (UV)-assisted vertical etching of polyethylene terephthalate (PET) for manufacturing microsystem components is reported. The PET vertical etching is achieved by using a dimethylformamide solution assisted by ultraviolet illumination onto a patterned PET substrate. The process is carried out in low temperature solutions for the benefits of low shrinkage and deformation of PET, yet having high aspect ratio structures and relatively high rates of etching. Furthermore, mask engineering is done for selecting an appropriate mask in order to have crack-free structures. This UV-assisted vertical etching of PET is suitable for the formation of plastic micro-parts as well as metal micro-parts with the aid of electrodeposition. Using this technique, a micromanipulator tool and an electrodeposition setup, all plastic and metallic microsystems can be easily manufactured and assembled. As an example prototype, we have successfully fabricated and assembled an all-plastic microturbine. This microturbine can be used in hydraulic or fluidic applications in microsystems.

  20. Bioinspired polyethylene terephthalate nanocone arrays with underwater superoleophobicity and anti-bioadhesion properties.

    PubMed

    Liu, Wendong; Liu, Xueyao; Fangteng, Jiaozi; Wang, Shuli; Fang, Liping; Shen, Huaizhong; Xiang, Siyuan; Sun, Hongchen; Yang, Bai

    2014-11-21

    This paper presents a facile method to fabricate bioinspired polyethylene terephthalate (PET) nanocone arrays via colloidal lithography. The aspect ratio (AR) of the nanocones can be finely modulated ranging from 1 to 6 by regulating the etching time. The samples with the AR value of 6 can present underwater superoleophobicity with the underwater oil contact angle (OCA) of 171.8°. The as-prepared PET nanocone arrays perform anti-bioadhesion behavior, which inhibits the formation of the actin cytoskeleton when it used as the substrate for cell culture. Moreover, the oil wettability is temperature controlled after modifying the PET nanocone arrays with PNIPAAm film, and the oil wettability of the functionalized nanocone arrays can be transformed from the superoleophobic state with OCA about 151° to the oleophilic state with OCA about 25° reversibly. Due to the high-throughput, parallel fabrication and cost-efficiency of this method, it will be favourable for researchers to introduce oleophobic properties to various substrate and device surfaces. Due to the superoleophobicity and simple functionalizing properties, the PET nanocone arrays are very promising surfaces for anti-adhesion, self-cleaning and have potential applications in material, medical, and biological fields. PMID:25303770

  1. Bacterial growth, detachment and cell size control on polyethylene terephthalate surfaces

    PubMed Central

    Wang, Liyun; Fan, Daming; Chen, Wei; Terentjev, Eugene M.

    2015-01-01

    In medicine and food industry, bacterial colonisation on surfaces is a common cause of infections and severe illnesses. However, the detailed quantitative information about the dynamics and the mechanisms involved in bacterial proliferation on solid substrates is still lacking. In this study we investigated the adhesion and detachment, the individual growth and colonisation, and the cell size control of Escherichia coli (E. coli) MG1655 on polyethylene terephthalate (PET) surfaces. The results show that the bacterial growth curve on PET exhibits the distinct lag and log phases, but the generation time is more than twice longer than in bulk medium. Single cells in the lag phase are more likely to detach than clustered ones in the log phase; clustered bacteria in micro-colonies have stronger adhesive bonds with surfaces and their neighbours with the progressing colonisation. We show that the cell size is under the density-dependent pathway control: when the adherent cells are at low density, the culture medium is responsible for coordinating cell division and cell size; when the clustered cells are at high population density, we demonstrate that the effect of quorum sensing causes the cell size decrease as the cell density on surfaces increases. PMID:26464114

  2. Staged replacement of the canine trachea with ringed polyethylene terephthalate grafts.

    PubMed

    Villegas-Cabello, O; Vázquez-Juárez, J L; Gutiérrez-Pérez, F M; Dávila-Córdova, R F; Díaz-Montemayor, C

    1994-10-01

    The reconstruction of extensive defects of the trachea ist best accomplished by the use of the patient's own tissue. Unfortunately, this is not always feasible and several prosthetic devices for replacement of the trachea have been described. In an experimental study staged tracheal replacements were performed in five dogs using a ringed polyethylene terephthalate (PET) tubular prosthesis previously cultured in the major omentum of the subjects. A set of stainless-steel arches embodied in silicone compound was designed to prevent collapse of the prosthesis. One of the subjects died on the 10th post-operative day of an unidentified cause and the remaining four eventually developed signs of respiratory distress. The cause of the respiratory insufficiency was anastomotic stenosis in every case. Infection, erosion, collapse or displacement were not observed. The rings designed to avoid collapse of the prosthesis represent a suitable alternative for use as external reinforcement in the tracheal situation. The PET grafts implanted as tracheal prosthesis according to the guidelines of this protocol consistently developed anastomotic stenosis and failed to support a functional respiratory epithelium. A further conclusion is that the use of absorbable sutures encourages anastomotic dehiscence and thus must be avoided. PMID:7863494

  3. An approach to the usage of polyethylene terephthalate (PET) waste as roadway pavement material.

    PubMed

    Gürü, Metin; Çubuk, M Kürşat; Arslan, Deniz; Farzanian, S Ali; Bilici, İbrahim

    2014-08-30

    This study investigates an application area for Polyethylene Terephthalate (PET) bottle waste which has become an environmental problem in recent decades as being a considerable part of the total plastic waste bulk. Two novel additive materials, namely Thin Liquid Polyol PET (TLPP) and Viscous Polyol PET (VPP), were chemically derived from waste PET bottles and used to modify the base asphalt separately for this aim. The effects of TLPP and VPP on the asphalt and hot mix asphalt (HMA) mixture properties were detected through conventional tests (Penetration, Softening Point, Ductility, Marshall Stability, Nicholson Stripping) and Superpave methods (Rotational Viscosity, Dynamic Shear Rheometer (DSR), Bending Beam Rheometer (BBR)). Also, chemical structures were described by Scanning Electron Microscope (SEM) equipped with Energy Dispersive Spectrometer (EDS) and Fourier Transform Infrared (FTIR) techniques. Since TLPP and VPP were determined to improve the low temperature performance and fatigue resistance of the asphalt as well as the Marshall Stability and stripping resistance of the HMA mixtures based on the results of the applied tests, the usage of PET waste as an asphalt roadway pavement material offers an alternative and a beneficial way of disposal of this ecologically hazardous material. PMID:25080154

  4. Solvent-Induced Crystallization in Poly(Ethylene Terephthalate) during Mass Transport

    NASA Astrophysics Data System (ADS)

    Ouyang, Hao

    2001-03-01

    The solvent transport in poly(ethylene terephthalate) (PET) and related phase transformation were investigated. The data of mass sorption were analyzed according to Harmon¡¦s model for Case I (Fickian), Case II (swelling) and anomalous transport. This transport process in PET is accompanied by the induced crystallization of the original amorphous state. The transformation was studied by wide angle x-ray scattering (WAXS), small angle x-ray scattering (SAXS), Differential Scanning Calorimeter (DSC), density gradient column, and Fourier Transform Infra-Red (FTIR). During this process, the matrix is under a compressive strain that causes different kinetic path of crystallization as compared to that by thermal annealing. This state of strain will assist the development of the solvent-induced crystallization. It also can be explained in terms of the principle of Le Chatelier if the local equilibrium is assumed. The model regarding the crystallization was proposed in terms of the study of long period L, the crystal thickness lc and the thickness of amorphous layer la, obtained from the linear correlation function and interface distribution function.

  5. Low-cost flexible supercapacitors based on laser reduced graphene oxide supported on polyethylene terephthalate substrate

    NASA Astrophysics Data System (ADS)

    Ghoniem, Engy; Mori, Shinsuke; Abdel-Moniem, Ahmed

    2016-08-01

    A controlled high powered CO2 laser system is used to reduce and pattern graphene oxide (GO) film supported onto a flexible polyethylene terephthalate (PET) substrate. The laser reduced graphene oxide (rGO) film is characterized and evaluated electrochemically in the absence and presence of an overlying anodicaly deposited thin film of pseuodcapactive MnO2 as electrodes for supercapacitor applications using aqueous electrolyte. The laser treatment of the GO film leads to an overlapped structure of defective multi-layer rGO sheets with an electrical conductivity of 273 S m-1. The rGO and MnO2/rGO electrodes exhibit specific capacitance in the range of 82-107 and 172-368 Fg-1 at applied current range of 0.1-1.0 mA cm-2 and retain 98 and 95% of their initial capacitances after 2000 cycles at a current density of 1.0 mA cm-2, respectively. Also, the rGO is assigned as an electrode material for flexible conventionally stacked and interdigitated in-plane supercapacitor structures using gel electrolyte. Three electrode architectures of 2, 4, and 6 sub-electrodes are studied for the interdigital in-plane design. The device with interdigital 6 sub-electrodes architecture I-PS(6) delivers power density of 537.1 Wcm-3 and an energy density of 0.45 mWh cm-3.

  6. Study of the Migration of Stabilizer and Plasticizer from Polyethylene Terephthalate into Food Simulants.

    PubMed

    Li, Bo; Wang, Zhi-Wei; Lin, Qin-Bao; Hu, Chang-Ying

    2016-07-01

    This study investigates the determination and migration of stabilizers and plasticizers from polyethylene terephthalate (PET). Two methods [ultrasonic extraction with dichloromethane or methanol and total dissolution with phenol/tetrachloroethane (m:m/1:1)] for pre-concentration of additives in PET material were performed. The diffusion of these additives from PET was evaluated by immersing in deionized water, acetic acid 3% (w/v), ethanol 20% (v/v), ethanol 50% (v/v) and isooctane at 20, 40, 55 and 70°C, respectively. The amount of additives in PET and food simulants was quantified by high-performance liquid chromatography-photodiode array detector (HPLC-PDA). The optimized HPLC method showed high correlation coefficients (R ≥ 0.9993), good precision, accuracy and reproducibility. Experimental diffusion coefficients (DP) were calculated according to a mathematical model based on Fick's second law, and the DP values of considered compounds ranged from 9.8 × 10(-15) to 1.4 × 10(-8) cm(2) s(-1) The experimental DP values were also compared with that predicted by currently used diffusion models. In addition, the effect of temperature on the diffusion rate was assessed. The effect of temperature on the diffusion coefficients followed an Arrhenius-type model with active energies ranged from 40.4 to 113.8 kJ mol(-1) for the target compounds. PMID:26941413

  7. A study of commercially-available polyethylene terephthalate (PET) and polycarbonate as nuclear track detector materials

    NASA Astrophysics Data System (ADS)

    Espinosa, G.; Golzarri, J. I.; Vazquez-Lopez, C.; Trejo, R.; Lopez, K.; Rickards, J.

    2014-07-01

    In the study of the sensitivity of materials to be used as nuclear track detectors, it was found that commercial polyethylene terephthalate (PET) from Ciel® water bottles, commercial roof cover polycarbonate, and recycled packaging strips (recycled PET), can be used as nuclear track detectors. These three commercial materials present nuclear tracks when bombarded by 2.27 MeV nitrogen ions produced in a Pelletron particle accelerator, and by fission fragments from a 252Cf source (79.4 and 103.8 MeV), after a chemical etching with a 6.25M KOH solution, or with a 6.25M KOH solution with 20% methanol, both solutions at 60±1°C. As an example, the nitrogen ions deposit approximately 1 keV/nm in the form of ionization and excitation at the surface of PET, as calculated using the SRIM code. The fission fragments deposit up to 9 keV/nm at the surface, in both cases generating sufficient free radicals to initiate the track formation process. However, 5 MeV alpha particles, typical of radon (222Rn) emissions, deposit only 0.12 keV/nm, do not present tracks after the chemical etching process. This valuable information could be very useful for further studies of new materials in nuclear track methodology.

  8. Separation of polyethylene terephthalate from municipal waste plastics by froth flotation for recycling industry.

    PubMed

    Wang, Chong-Qing; Wang, Hui; Liu, You-Nian

    2015-01-01

    Recycling is an effective way to manage plastic wastes and receives considerable attention. Since plastic mixtures are difficult to recycle because of their intrinsic characteristics, separation of mixed plastics is the key problem for recycling. Separation of polyethylene terephthalate (PET) from municipal waste plastics (MWP) by froth flotation combined with alkaline pretreatment was investigated for recycling industry. The effect of process variables was estimated by L9 (3(4)) orthogonal array of experiments and single factor experiments. The optimum conditions of alkaline pretreatment are 10 wt% sodium hydroxide, 20 min and 70°C. After alkaline pretreatment under optimum conditions, flotation separation PET from acrylonitrile-butadiene-styrene, polystyrene, polycarbonate or polyvinyl chloride was achieved with high purity and efficiency. The purity of PET is up to 98.46% and the recovery is above 92.47%. A flow sheet of separation PET from MWP by a combination of froth flotation and sink float separation was designed. This study facilitates industrial application of plastics flotation and provides technical insights into recycling of waste plastics. PMID:25449606

  9. [Interlaboratory study on migration test of antimony and germanium for food-contact polyethylene terephthalate].

    PubMed

    Murakami, Ryo; Mutsuga, Motoh; Abe, Takashi; Abe, Yutaka; Ohsaka, Ikue; Ohno, Haruka; Ohno, Hiroyuki; Ohno, Yuichiro; Ozaki, Asako; Kakihara, Yoshiteru; Kawasaki, Hiromi; Kobayashi, Hisashi; Shibata, Hiroshi; Shirono, Katsuhiro; Sekido, Haruko; Sonobe, Hironori; Takasaka, Noriko; Tajima, Yoshiyasu; Tanaka, Aoi; Tanaka, Hideyuki; Nomura, Chie; Haneishi, Nahoko; Hikida, Akinori; Miura, Toshihiko; Watanabe, Kazunari; Akiyama, Hiroshi

    2015-01-01

    An interlaboratory study was performed to evaluate a migration test method of antimony (Sb) and germanium (Ge), based on the Japanese Food Sanitation Law for food- contact polyethylene terephthalate. Eighteen laboratories participated, and quantified Sb and Ge in three test solutions as blind duplicates using graphite furnace atomic absorption spectrometry (GF-AAS), inductively coupled plasma-optical emission spectrometry (ICP-OES) or induced coupled plasma-mass spectrometry (ICP-MS). Statistical analysis revealed that the trueness, repeatability and reproducibility were 98-107%, 1.7-7.5% and 2.0-18.8% by using GF-AAS and ICP-OES. The performance of these methods is sufficient for testing the specifications. The performance parameters of ICP-MS were 99-106%, 0.7-2.2% and 2.2-10.5%, respectively. ICP-MS is available as an alternative measuring method. However, in some laboratories, the quantitative values of Sb were higher than the addition levels. We found that Sb in working solutions is absorbed on glass vessels. Careful control of concentration in working solutions is required for Sb analysis. PMID:25925077

  10. Effect of micro-patterning on bacterial adhesion on polyethylene terephthalate surface.

    PubMed

    Wang, Liyun; Chen, Wei; Terentjev, Eugene

    2015-05-01

    Bacterial adhesion on surfaces commonly used in medicine and food industry could lead to infections and illnesses. Topographically patterned surfaces recently have shown to be a promising alternative to chemical antibacterial methods, which might release cytotoxin and promote antibiotic resistance. In this study, we fabricated micro-patterned polyethylene terephthalate surfaces, and quantitatively explored the amount and localization of Escherichia coli MG1655 cells attached on a series of defined topographies. The adhesion was conducted in static conditions and under a weak flow, in both physiological buffer and nutritious solutions. The results showed that in the presence of weak shear force, live bacteria could still maintain sensing ability in nutritious culture, but not in buffer solution. The finely textured surface, which could inhibit bacterial adhesion in the early stage of attachment, reversed its effect to enhance the adhesion after 24 h incubation, indicating that microbial cells seemed to be able to sense the disadvantageous condition and eventually overcome it. In terms of adhesion localization, bacteria exhibited preferential adhesion onto the edges of topographic features. The patterned substrates that have the most even (homogeneous) bacterial localization on topographic features retained the least attachment after 24 h exposure. PMID:25515774

  11. Surface modification of poly(ethylene terephthalate) fabric via photo-chemical reaction of dimethylaminopropyl methacrylamide

    NASA Astrophysics Data System (ADS)

    Mohamed, Nasser H.; Bahners, Thomas; Wego, Andreas; Gutmann, Jochen S.; Ulbricht, Mathias

    2012-10-01

    Photo-chemical reactions and surface modifications of poly(ethylene terephthalate) (PET) fabrics with the monomer dimethylaminopropyl methacrylamide (DMAPMA) and benzophenone (BP) as photo-initiator using a broad-band UV lamp source were investigated. The tertiary amino groups of the grafted poly(DMAPMA) chains were subsequently quaternized with alkyl bromides of different chain lengths to establish antibacterial activity. The surface composition, structure and morphology of modified PET fabrics were characterized by Fourier transform infrared spectroscopy (FTIR/ATR), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). To evaluate the amount of quaternary and tertiary ammonium groups on the modified surface, PET was dyed with an acid dye which binds to the ammonium groups. Therefore, the color depth is a direct indicator of the amount of ammonium groups. The resulting antibacterial activity of the modified PET fabrics was tested with Escherichia coli. The results of all experiments show that a photochemical modification of PET is possible using DMAPMA, benzophenone and UV light. Also, the quaternization of tertiary amino groups as well as the increase in antibacterial activity of the modified PET by the established quaternary ammonium groups were successful.

  12. Durable grafting of silkworm pupa protein onto the surface of polyethylene terephthalate fibers.

    PubMed

    Zhou, Jianfeng; Zheng, Dandan; Zhang, Fengxiu; Zhang, Guangxian

    2016-12-01

    In this paper, reactive -NH2 groups (8.36×10(-6)mol/g fabric) were introduced to the surface of polyethylene terephthalate (PET) fabrics by a nitration and reduction method, and epoxy groups were introduced to silkworm pupa protein (SPP) by reaction with epoxy chloropropane. PET-SPP composite fabrics were then prepared by reaction of these two precursors. The results showed that the SPP was firmly grafted onto the PET fabric surface and that the hydrophilicity of the fabric was markedly improved by the grafting of SPP. SEM images revealed a layer of substance covering the surface of the PET fibers, and XPS investigation showed that the nitrogen content of the PET-SPP fabric was higher than that of the original PET fabric (2.32% vs 0%). ATR-FTIR adsorption bands at 1653 and 1543cm(-1) suggested the successful grafting of SPP onto the PET fabric surface. The DSC and TG of the PET fibers demonstrated that the thermal stability of the original PET fibers was maintained well by the SPP-grafted PET fibers. The breaking strength, bending rigidity, air permeability, and crease recovery angle of the original PET fabric were also retained by the SPP-grafted PET fabric. PMID:27612829

  13. Flexible piezoelectric pressure sensors using oriented aluminum nitride thin films prepared on polyethylene terephthalate films

    NASA Astrophysics Data System (ADS)

    Akiyama, Morito; Morofuji, Yukari; Kamohara, Toshihiro; Nishikubo, Keiko; Tsubai, Masayoshi; Fukuda, Osamu; Ueno, Naohiro

    2006-12-01

    We have investigated the high sensitive piezoelectric response of c-axis oriented aluminum nitride (AlN) thin films prepared on polyethylene terephthalate (PET) films. The AlN films were deposited using a radio frequency magnetron sputtering method at temperatures close to room temperature. The c axes of the AlN films were perpendicularly oriented to the PET film surfaces. The sensor consisting of the AlN and PET films is flexible like PET films and the electrical charge is linearly proportional to the stress within a wide range from 0to8.5MPa. The sensor can respond to the frequencies from 0.3 to over 100Hz and measures a clear human pulse wave form by holding the sensor between thumb and middle finger. The resolution of the pulse wave form is comparable to a sphygmomanometer at stress levels of 10kPa. We think that the origin of the high performance of the sensor is the deflection effect, the thin thickness and high elastic modulus of the AlN layer, and the thin thickness and low elastic modulus of the PET film.

  14. Separation of polyethylene terephthalate from municipal waste plastics by froth flotation for recycling industry

    SciTech Connect

    Wang, Chong-Qing; Wang, Hui Liu, You-Nian

    2015-01-15

    Highlights: • Factors of NaOH treatment were studied by orthogonal and single factor experiments. • Mechanism of alkaline treatment for facilitating flotation was manifested. • Flotation separation of PET was achieved with high purity and efficiency. • A flow sheet of purification PET from MWP was designed. - Abstract: Recycling is an effective way to manage plastic wastes and receives considerable attention. Since plastic mixtures are difficult to recycle because of their intrinsic characteristics, separation of mixed plastics is the key problem for recycling. Separation of polyethylene terephthalate (PET) from municipal waste plastics (MWP) by froth flotation combined with alkaline pretreatment was investigated for recycling industry. The effect of process variables was estimated by L{sub 9} (3{sup 4}) orthogonal array of experiments and single factor experiments. The optimum conditions of alkaline pretreatment are 10 wt% sodium hydroxide, 20 min and 70 °C. After alkaline pretreatment under optimum conditions, flotation separation PET from acrylonitrile–butadiene–styrene, polystyrene, polycarbonate or polyvinyl chloride was achieved with high purity and efficiency. The purity of PET is up to 98.46% and the recovery is above 92.47%. A flow sheet of separation PET from MWP by a combination of froth flotation and sink float separation was designed. This study facilitates industrial application of plastics flotation and provides technical insights into recycling of waste plastics.

  15. In situ synthesis of TiO2/polyethylene terephthalate hybrid nanocomposites at low temperature

    NASA Astrophysics Data System (ADS)

    Peng, Xinyan; Ding, Enyong; Xue, Feng

    2012-06-01

    TiO2 nanoflowers were in situ grown on polyethylene terephthalate (PET) non-woven fabric by hydrolysis of TiCl4 in aqueous solution in the presence of nanocrystal cellulose grafted PET fabric (NCC-g-PET) at a low temperature of 70 °C. Nanocrystal cellulose (NCC) pre-grafted on PET fabric acted as hydrophilic substrate and morphology inducing agent to promote the nucleation and crystal growth of TiO2. Detailed information on the synthetic process was presented. The resulting samples were characterized using FE-SEM, EDS, ATR-IR, Raman microscopy, XRD and TG analysis. The photocatalytic activity of the samples was evaluated by the degradation of orange methyl under solar light. Characteristic results indicate that rutile TiO2 nanoflowers have grown abundantly on PET non-woven fabric, and the established hydrogen bonding strengthens the interfacial interaction between the inorganic particles and the polymeric substrates. The methyl orange decoloration test under natural solar light demonstrates that this TiO2/PET hybrid nanocomposites exhibit excellent self-cleaning performance which is expected to have a good potential for commercialization.

  16. Morphology and Mechanical Properties of Poly(Ethylene Terephthalate) Stretched Above the Glass Transition Temperature

    NASA Astrophysics Data System (ADS)

    Todorov, Lyudmil V.; Viana, Júlio C.

    2007-04-01

    This study presents an experimental investigation into the development of the strain-induced morphology of amorphous poly(ethylene terephthalate), PET, stretched above its glass transition temperature. The present work aims at: i) defining the most important processing parameters that govern the structure formation and its significance; ii) characterising the mechanical properties of uniaxial stretched glassy PET, as an approach for industrial stretch-blow moulding techniques; iii) establishing structure-properties relationships. Compression moulded amorphous PET was uniaxial stretched with variations of following stretching parameters: stretching temperature, Tst, stretching velocity, Vst, and stretching ratio, λst, that were varied in two levels according to a L8 Taguchi orthogonal array. The developed morphologies were observed by differential scanning calorimetry (DSC), birefringence and Wide-Angle X-ray Scattering (WAXS). The mechanical behaviour was assessed in tensile testing at 15 mm.min-1 and room temperature. The results were treated by a statistical ANOVA tool. A strong thermal and mechanical coupling is evidenced in the stretching process, significantly influencing the morphology development. The main stretching parameters controlling microstructure formation were defined. The relationships between the microstructure and mechanical properties were established too.

  17. Morphological Evolution of Semi-crystalline Poly(ethylene terephthalate) During Large Scale Simple Shear Deformation

    NASA Astrophysics Data System (ADS)

    Xia, Zhiyong; Sue, Hung-Jue

    2001-03-01

    In this study, the morphological evolution of semi-crystalline poly(ethylene terephthalate) (PET) under large scale simple shear is investigated. The equal channel angular extrusion (ECAE) process is used to induce the simple shear deformation. The deformation of semi-crystalline PET at different length scales is studied. At the spherulite scale, optical microscopy (OM) and scanning electron microscopy (SEM) are used. Lamellar scale information is obtained by small-angle X-ray scattering (SAXS) and transmission electron microscopy (TEM). Molecular chains in the crystalline lamellae are obtained by wide-angle X-ray scattering (WAXS), and the molecular chains in the amorphous phase are studied by annealing the sample at temperatures above glass transition but below melting point. Structural characterization shows that PET spherulites are highly elongated into macrofibrils after ECAE. Within the macrofibrils, a "V-type" of crystalline lamellar orientation is induced. Molecular chains in the crystalline lamellae are tilted to the lamellar surface, whereas the molecular chains in the amorphous phase are highly stretched.

  18. Plasma nano-modification of poly(ethylene terephthalate) fabric for pigment adhesion enhancement.

    PubMed

    Pransilp, Porntepin; Kiatkamjornwong, Suda; Bhanthumnavin, Worawan; Paosawatyanyong, Boonchoat

    2012-01-01

    Poly(ethylene terephthalate) (PET) fabrics were modified by treating with radio frequency (RF) plasma of different gases, including argon (Ar), nitrogen (N2), oxygen (O2) and sulfur hexafluoride (SF6), under varied power (50-150 watt) and time period (0.5-20 min). Observations indicated that plasma has affected the morphology and roughness of PET fiber surface in the nano-scale level. After plasma treatment, test patterns were printed by inkjet printer directly onto the sample surface. The enhancement of color printing performance on PET fabric by plasma treatment was evaluated by color spectroscopy. The surface nano-modified PET fabrics by Ar, N2, O2, and SF6 plasmas all exhibited enhanced color yield. AFM, SEM, FTIR-ATR and XPS results suggested that the improved pigment color yield was neither clearly contributed by the wettability of the fabrics nor the polar group induced onto the fiber surfaces but rather mainly by the alteration of surface roughness. PMID:22524006

  19. Human mesenchymal stromal cell-enhanced osteogenic differentiation by contact interaction with polyethylene terephthalate nanogratings.

    PubMed

    Antonini, Sara; Meucci, Sandro; Parchi, Paolo; Pacini, Simone; Montali, Marina; Poggetti, Andrea; Lisanti, Michele; Cecchini, Marco

    2016-01-01

    Among the very large number of polymeric materials that have been proposed in the field of orthopedics, polyethylene terephthalate (PET) is one of the most attractive thanks to its flexibility, thermal resistance, mechanical strength and durability. Several studies have been proposed that interface nano- or micro-structured surfaces with mesenchymal stromal cells (MSCs), demonstrating the potential of this technology for promoting osteogenesis. All these studies were carried out on biomaterials other than PET, which remains almost uninvestigated in terms of cell shaping, alignment and differentiation. Here, we study the effect of PET 350-depth nanogratings (NGs) with a ridge and lateral groove size of 500 nm (T1) or 1 μm (T2), on bone marrow-derived human MSC (hMSC) differentiation in relation to the osteogenic fate. We demonstrate that these substrates, especially T2, can promote the osteogenic phenotype more efficiently than standard flat surfaces and that this effect is more marked if cells are cultured in osteogenic medium than in basal medium. Finally, we show that the shape and disposition of calcium hydroxyapatite granules on the different substrates was influenced by the substrate symmetry, being more elongated and spatially organized on NGs than on flat surfaces. PMID:27388559

  20. Up-cycling of PET (polyethylene terephthalate) to the biodegradable plastic PHA (polyhydroxyalkanoate).

    PubMed

    Kenny, Shane T; Runic, Jasmina Nikodinovic; Kaminsky, Walter; Woods, Trevor; Babu, Ramesh P; Keely, Chris M; Blau, Werner; O'Connor, Kevin E

    2008-10-15

    The conversion of the petrochemical polymer polyethylene terephthalate (PET) to a biodegradable plastic polyhydroxyal-kanoate (PHA) is described here. PET was pyrolised at 450 degrees C resulting in the production of a solid, liquid, and gaseous fraction. The liquid and gaseous fractions were burnt for energy recovery, whereas the solid fraction terephthalic acid (TA) was used as the feedstock for bacterial production of PHA. Strains previously reported to grow on TA were unable to accumulate PHA. We therefore isolated bacteria from soil exposed to PET granules at a PET bottle processing plant From the 32 strains isolated, three strains capable of accumulation of medium chain length PHA (mclPHA) from TA as a sole source of carbon and energy were selected for further study. These isolates were identified using 16S rDNA techniques as P. putida (GO16), P. putida (GO19), and P. frederiksbergensis (GO23). P. putida GO16 and GO19 accumulate PHA composed predominantly of a 3-hydroxydecanoic acid monomer while P. frederiksbergensis GO23 accumulates 3-hydroxydecanoic acid as the predominant monomer with increased amounts of 3-hydroxydodecanoic acid and 3-hydroxydodecenoic acid compared to the other two strains. PHA was detected in all three strains when nitrogen depleted below detectable levels in the growth medium. Strains GO16 and GO19 accumulate PHA at a maximal rate of approximately 8.4 mg PHA/l/h for 12 h before the rate of PHA accumulation decreased dramatically. Strain GO23 accumulates PHA at a lower maximal rate of 4.4 mg PHA/l/h but there was no slow down in the rate of PHA accumulation over time. Each of the PHA polymers is a thermoplastic with the onset of thermal degradation occurring around 308 degrees C with the complete degradation occurring by 370 degrees C. The molecular weight ranged from 74 to 123 kDa. X-ray diffraction indicated crystallinity of the order of 18-31%. Thermal analysis shows a low glass transition (-53 degrees C) with a broad melting

  1. Biological and Tribological Assessment of Poly(Ethylene Oxide Terephthalate)/Poly(Butylene Terephthalate), Polycaprolactone, and Poly (L\\DL) Lactic Acid Plotted Scaffolds for Skeletal Tissue Regeneration.

    PubMed

    Hendrikson, Wilhelmus J; Zeng, Xiangqiong; Rouwkema, Jeroen; van Blitterswijk, Clemens A; van der Heide, Emile; Moroni, Lorenzo

    2016-01-21

    Additive manufactured scaffolds are fabricated from three commonly used biomaterials, polycaprolactone (PCL), poly (L\\DL) lactic acid (P(L\\DL)LA), and poly(ethylene oxide terephthalate)/poly(butylene terephthalate) (PEOT/PBT). Scaffolds are compared biologically and tribologically. Cell-seeded PEOT/PBT scaffolds cultured in osteogenic and chondrogenic differentiation media show statistical significantly higher alkaline phosphatase (ALP) activity/DNA and glycosaminoglycans (GAG)/DNA ratios, followed by PCL and P(L\\DL)LA scaffolds, respectively. The tribological performance is assessed by determining the friction coefficients of the scaffolds at different loads and sliding velocities. With increasing load or decreasing sliding velocity, the friction coefficient value decreases. PEOT/PBT show to have the lowest friction coefficient value, followed by PCL and P(L\\DL)LA. The influence of the scaffold architecture is further determined with PEOT/PBT. Reducing of the fiber spacing results in a lower friction coefficient value. The best and the worst performing scaffold architecture are chosen to investigate the effect of cell culture on the friction coefficient. Matrix deposition is low in the cell-seeded scaffolds and the effect is, therefore, undetermined. Taken together, our studies show that PEOT/PBT scaffolds support better skeletal differentiation of seeded stromal cells and lower friction coefficient compared to PCL and P(L/DL)A scaffolds. PMID:26775915

  2. Bioinspired polyethylene terephthalate nanocone arrays with underwater superoleophobicity and anti-bioadhesion properties

    NASA Astrophysics Data System (ADS)

    Liu, Wendong; Liu, Xueyao; Fangteng, Jiaozi; Wang, Shuli; Fang, Liping; Shen, Huaizhong; Xiang, Siyuan; Sun, Hongchen; Yang, Bai

    2014-10-01

    This paper presents a facile method to fabricate bioinspired polyethylene terephthalate (PET) nanocone arrays via colloidal lithography. The aspect ratio (AR) of the nanocones can be finely modulated ranging from 1 to 6 by regulating the etching time. The samples with the AR value of 6 can present underwater superoleophobicity with the underwater oil contact angle (OCA) of 171.8°. The as-prepared PET nanocone arrays perform anti-bioadhesion behavior, which inhibits the formation of the actin cytoskeleton when it used as the substrate for cell culture. Moreover, the oil wettability is temperature controlled after modifying the PET nanocone arrays with PNIPAAm film, and the oil wettability of the functionalized nanocone arrays can be transformed from the superoleophobic state with OCA about 151° to the oleophilic state with OCA about 25° reversibly. Due to the high-throughput, parallel fabrication and cost-efficiency of this method, it will be favourable for researchers to introduce oleophobic properties to various substrate and device surfaces. Due to the superoleophobicity and simple functionalizing properties, the PET nanocone arrays are very promising surfaces for anti-adhesion, self-cleaning and have potential applications in material, medical, and biological fields.This paper presents a facile method to fabricate bioinspired polyethylene terephthalate (PET) nanocone arrays via colloidal lithography. The aspect ratio (AR) of the nanocones can be finely modulated ranging from 1 to 6 by regulating the etching time. The samples with the AR value of 6 can present underwater superoleophobicity with the underwater oil contact angle (OCA) of 171.8°. The as-prepared PET nanocone arrays perform anti-bioadhesion behavior, which inhibits the formation of the actin cytoskeleton when it used as the substrate for cell culture. Moreover, the oil wettability is temperature controlled after modifying the PET nanocone arrays with PNIPAAm film, and the oil wettability of the

  3. Improvement of barrier properties of poly(ethylene terephthalate)/organoclay nanocomposites

    NASA Astrophysics Data System (ADS)

    Dini, Maryam

    The presence of nanoclays in poly(ethylene terephthalate) (PET) as an impermeable phase and for increasing the tortuous path of permeates can result in outstanding property improvements in terms of decreasing gas permeability. PET nanocomposites can be prepared by in-situ or melt-mixing methods. The latter approach is more economical, practical and environmental friendly due to the absence of monomers and/or organic solvents. The microstructure of polymer nanocomposites substantially plays an important role in the determining macroscopic properties of final products. To achieve significant performance enhancements, good dispersion of the nanoclay in the matrix and thermodynamic compatibility between the nanoclay and the polymer are required. In this work, poly(ethylene terephthalate) (PET) nanocomposites were prepared by water-assisted melt compounding in a twin-screw extruder. In order to facilitate the diffusion of PET molecules into clay galleries, steam was fed into the extruder. Subsequently, the molecular weight (M W) reduction of the PET matrix, due to hydrolysis by water, was compensated by solid-state polymerization (SSP). Effects of feeding rate, compatibility between PET and nanoclay (Cloisite Na+, Cloisite 30B and Nanomer I.28E) and SSP on the microstructure of the nanocomposites were studied. The results revealed more delamination of organoclay platelets in PET-C30B nanocomposites processed at low feeding rate compared to those processed at high feeding rate. The presence of water resulted in a larger number of single and double layers of C30B nanoparticles as well as an increased aspect ratio of clay particles in PET nanocomposites. The effect of water on the microstructure of PET nanocomposites was strongly dependent on the nanoclay modifier. Processing with water had negative effects on the PET-I28E nanocomposites, because of its lower compatibility. Studies on the structure of PET after SSP by rheological measurements, Nuclear magnetic resonance

  4. Decontamination efficiency of a new post-consumer poly(ethylene terephthalate) (PET) recycling concept.

    PubMed

    Welle, Frank

    2008-01-01

    The aim of the study was to investigate and evaluate the cleaning efficiency of a new recycling concept for post-consumer poly(ethylene terephthalate) (PET). The so-called Flake To Resin (FTR) recycling process produces PET pellets or preforms from conventionally recycled PET flakes for the application in new PET packaging in direct food contact. The investigated process can be considered as 'super-clean' recycling process and was developed to introduce conventional recycled post-consumer (PCR) PET flakes up to an amount of 50% into the pellet and preform production. Within the study the cleaning efficiency of the investigated FTR process was determined by a challenge test. The experimental results obtained from three challenge tests with different input concentrations of the surrogates and different amounts of post-consumer PET flakes show that all applied surrogates are very efficiently removed by the investigated recycling process. The cleaning efficiencies for all surrogates are above 99.9%. In the final product of the process no surrogates could be determined above the detection limits (0.5 mg kg(-1)) even if the initial concentrations were in the percentage range. From a migrational point the final product, which are either PET pellets or preforms, was similar to virgin PET. Only the PET typical substances acetaldehyde and ethylene glycol had slightly higher concentrations than found in a conventional PET virgin sample used as reference. The generally accepted migration limit of 10 microg kg(-1) for the surrogates in the final products of the challenge tests is established for all kinds of foodstuffs. PMID:17906995

  5. Ideonella sakaiensis sp. nov., isolated from a microbial consortium that degrades poly(ethylene terephthalate).

    PubMed

    Tanasupawat, Somboon; Takehana, Toshihiko; Yoshida, Shosuke; Hiraga, Kazumi; Oda, Kohei

    2016-08-01

    A Gram-stain-negative, aerobic, non-spore-forming, rod-shaped bacterium, designed strain 201-F6T, was isolated from a microbial consortium that degrades poly(ethylene terephthalate) (PET) collected in Sakai city, Japan, and was characterized on the basis of a polyphasic taxonomic study. The cells were motile with a polar flagellum. The strain contained cytochrome oxidase and catalase. It grew within the pH range 5.5-9.0 (optimally at pH 7-7.5) and at 15-42 ºC (optimally at 30-37 ºC). The major isoprenoid quinone was ubiquinone with eight isoprene units (Q-8). C16 : 0, C17 : 0 cyclo, C18 :1ω7c and C12 : 0 2-OH were the predominant cellular fatty acids. The major polar lipids were phosphatidylethanolamine, lyso-phosphatidylethanolamine, phosphatidylglycerol and diphosphatidylglycerol. The G+C content of genomic DNA was 70.4 mol%. Phylogenetic analysis using the 16S rRNA gene sequences showed that strain 201-F6T was affiliated to the genus Ideonella, and was closely related to Ideonella dechloratans LMG 28178T (97.7 %) and Ideonella azotifigens JCM 15503T (96.6 %). Strain 201-F6T could be clearly distinguished from the related species of the genus Ideonella by its physiological and biochemical characteristics as well as by its phylogenetic position and DNA-DNA relatedness. Therefore, the strain represents a novel species of the genus Ideonella, for which the name Ideonella sakaiensis sp. nov. (type strain 201-F6T=NBRC 110686T=TISTR 2288T) is proposed. PMID:27045688

  6. DC bias effect on alternating current electrical conductivity of poly(ethylene terephthalate)/alumina nanocomposites

    NASA Astrophysics Data System (ADS)

    Nikam, Pravin N.; Deshpande, Vineeta D.

    2016-05-01

    Polymer nanocomposites based on metal oxide (ceramic) nanoparticles are a new class of materials with unique properties and designed for various applications such as electronic device packaging, insulation, fabrication and automotive industries. Poly(ethylene terephthalate) (PET)/alumina (Al2O3) nanocomposites with filler content between 1 wt% and 5 wt% were prepared by melt compounding method using co-rotating twin screw extruder and characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and precision LCR meter techniques. The results revealed that proper uniform dispersion at lower content up to 2 wt% of nano-alumina observed by using TEM. Aggregation of nanoparticles was observed at higher content of alumina examined by using SEM and TEM. The frequency dependences of the alternating current (AC) conductivity (σAC) of PET/alumina nanocomposites on the filler content and DC bias were investigated in the frequency range of 20Hz - 1MHz. The results showed that the AC and direct current (DC) conductivity increases with increasing DC bias and nano-alumina content upto 3 wt%. It follows the Jonscher's universal power law of solids. It revealed that σAC of PET/alumina nanocomposites can be well characterized by the DC conductivity (σDC), critical frequency (ωc), critical exponent of the power law (s). Roll of DC bias potential led to an increase of DC conductivity (σDC) due to the creation of additional conducting paths with the polymer nanocomposites and percolation behavior achieved through co-continuous morphology.

  7. Diffusion behaviour of the acetaldehyde scavenger 2-aminobenzamide in polyethylene terephthalate for beverage bottles.

    PubMed

    Franz, Roland; Gmeiner, Margit; Gruner, Anita; Kemmer, Diana; Welle, Frank

    2016-01-01

    Polyethylene terephthalate (PET) bottles are widely used as packaging material for natural mineral water. However, trace levels of acetaldehyde can migrate into natural mineral water during the shelf life and might influence the taste of the PET bottled water. 2-Aminobenzamide is widely used during PET bottle production as a scavenging agent for acetaldehyde. The aim of this study was the determination of the migration kinetics of 2-aminobenzamide into natural mineral water as well as into 20% ethanol. From the migration kinetics, the diffusion coefficients of 2-aminobenzamide in PET at 23 and 40°C were determined to be 4.2 × 10(-)(16) and 4.2 × 10(-)(15) cm(2) s(-1), respectively. The diffusion coefficient for 20% ethanol at 40°C was determined to be 7.7 × 10(-)(15) cm(2) s(-1), which indicates that 20% ethanol is causing swelling of the PET polymer. From a comparison of migration values between 23 and 40°C, acceleration factors of 9.7 when using water as contact medium and 18.1 for 20% ethanol as simulant can be derived for definition of appropriate accelerated test conditions at 40°C. The European Union regulatory acceleration test based on 80 kJ mol(-1) as conservative activation energy overestimates the experimentally determined acceleration rates by a factor of 1.6 and 3.1, respectively. PMID:26666986

  8. Diffusion behaviour of the acetaldehyde scavenger 2-aminobenzamide in polyethylene terephthalate for beverage bottles

    PubMed Central

    Franz, Roland; Gmeiner, Margit; Gruner, Anita; Kemmer, Diana; Welle, Frank

    2016-01-01

    ABSTRACT Polyethylene terephthalate (PET) bottles are widely used as packaging material for natural mineral water. However, trace levels of acetaldehyde can migrate into natural mineral water during the shelf life and might influence the taste of the PET bottled water. 2-Aminobenzamide is widely used during PET bottle production as a scavenging agent for acetaldehyde. The aim of this study was the determination of the migration kinetics of 2-aminobenzamide into natural mineral water as well as into 20% ethanol. From the migration kinetics, the diffusion coefficients of 2-aminobenzamide in PET at 23 and 40°C were determined to be 4.2 × 10− 16 and 4.2 × 10− 15 cm2 s–1, respectively. The diffusion coefficient for 20% ethanol at 40°C was determined to be 7.7 × 10− 15 cm2 s–1, which indicates that 20% ethanol is causing swelling of the PET polymer. From a comparison of migration values between 23 and 40°C, acceleration factors of 9.7 when using water as contact medium and 18.1 for 20% ethanol as simulant can be derived for definition of appropriate accelerated test conditions at 40°C. The European Union regulatory acceleration test based on 80 kJ mol–1 as conservative activation energy overestimates the experimentally determined acceleration rates by a factor of 1.6 and 3.1, respectively. PMID:26666986

  9. MeV H+ ion irradiation effect on the stoichiometry of polyethylene terephthalate films

    NASA Astrophysics Data System (ADS)

    Abdesselam, M.; Muller, D.; Djebara, M.; Ouichaoui, S.; Chami, A. C.

    2013-07-01

    Appropriate experimental conditions have been chosen to investigate the influence of main H+ ion irradiation parameters on stoichiometry changes induced in polyethylene terephthalate (PET) thin films. Stacks of six self-supporting identical films were irradiated perpendicularly to the target surface. Thus, the irradiations were realized simultaneously at different values of the target electronic stopping power, ɛ+. Indeed, the initial H+ ion energy of 1.1 MeV incident on the front polymer film was degraded down to 0.48 MeV at the entrance of the rear stacked film, which corresponds to an increase of ɛ+ from ˜0.22 up to ˜0.41 MeV cm2 mg-1. Ion fluences in the range (0.05-4) × 1015 cm-2 corresponding to an ion dose interval 1.80-263 MGy were used. The (H, O, C) atomic surface densities of the PET polymeric films were quantitatively determined by IBA techniques using a 1.62 MeV deuteron beam leading to the following main results: for each target film stacked at a given position thus fixed ɛ+, the oxygen atomic density decreases linearly versus ion fluence, ϕ; for the different ɛ+, the hydrogen impoverishment of the PET target is insignificant below critical fluence ϕc ˜ 1.5 × 1015 cm-2 and becomes substantial above ϕc; for fixed ϕ, the hydrogen and oxygen atomic densities exhibit linear decreases versus ɛ+; all measured such data versus ϕ and ɛ+ merge together into a unique decreasing curve for each (H, O, C) polymer content element when represented in function of the H+ ion dose, D, tightly correlating the latter two parameters; the O content element release from the PET target appears to be the most important, followed by the H content depletion, while the target C content is least affected under H+ ion irradiation.

  10. Enhancement of Polyethylene Terephthalate Artificial Ligament Graft Osseointegration using a Periosteum Patch in a Goat Model.

    PubMed

    Dai, Z; Bao, W; Li, S; Li, H; Jiang, J; Chen, S

    2016-06-01

    The purpose of this study is to investigate whether a periosteum patch could enhance polyethylene terephthalate (PET) artificial ligament graft osseointegration in a bone tunnel. 12 female goats underwent ACL reconstruction with a PET artificial ligament graft in the right knees. Right knees in 6 goats were reconstructed with periosteum patch-enveloped PET grafts (Periosteum group) in the tibia bone tunnel, whereas the other 6 goats had no periosteum patch and served as the Control group. All the goats were sacrificed at 12 months after surgery. 3 tibial-graft complex samples in each group were harvested consecutively for microcomputed tomography (micro-CT) scan, magnetic resonance imaging (MRI) scan and histological evaluation. The other 3 tibial-graft complex samples in each group were harvested for biomechanical testing. The mean pull-out load of the Periosteum group (208±25 N) at 12 months was significantly higher than that of the Control group (107±13 N) (p=0.0044). According to the micro-CT scan, more new bone formation was observed at the graft-bone interface in the Periosteum group compared with the Control group. Furthermore, MRI showed that the Periosteum group appeared to have a better graft osseointegration within the bone tunnel compared with the Control group. Histologically, application of a periosteum patch induced more new bone and Sharpey's fiber formation between the graft and bone tunnel compared with the controls. The study has shown that periosteum enveloping of the PET artificial ligament has a positive effect in the induction of artificial ligament osseointegration within the bone tunnel. PMID:26990720

  11. Gas barrier properties of titanium oxynitride films deposited on polyethylene terephthalate substrates by reactive magnetron sputtering

    NASA Astrophysics Data System (ADS)

    Lin, M.-C.; Chang, L.-S.; Lin, H. C.

    2008-03-01

    Titanium oxynitride (TiN xO y) films were deposited on polyethylene terephthalate (PET) substrates by means of a reactive radio frequency (RF) magnetron sputtering system in which the power density and substrate bias were the varied parameters. Experimental results show that the deposited TiN xO y films exhibited an amorphous or a columnar structure with fine crystalline dependent on power density. The deposition rate increases significantly in conjunction as the power density increases from 2 W/cm 2 to 7 W/cm 2. The maximum deposition rate occurs, as the substrate bias is -40 V at a certain power densities chosen in this study. The film's roughness slightly decreases with increasing substrate bias. The TiN xO y films deposited at power densities above 4 W/cm 2 show a steady Ti:N:O ratio of about 1:1:0.8. The water vapor and oxygen transmission rates of the TiN xO y films reach values as low as 0.98 g/m 2-day-atm and 0.60 cm 3/m 2-day-atm which are about 6 and 47 times lower than those of the uncoated PET substrate, respectively. These transmission rates are comparable to those of DLC, carbon-based and Al 2O 3 barrier films. Therefore, TiN xO y films are potential candidates to be used as a gas permeation barrier for PET substrate.

  12. Study on the leaching of phthalates from polyethylene terephthalate bottles into mineral water.

    PubMed

    Keresztes, Szilvia; Tatár, Enikő; Czégény, Zsuzsanna; Záray, Gyula; Mihucz, Victor G

    2013-08-01

    Carbonated and non-carbonated mineral water samples bottled in 0.5-L, 1.5-L and 2.0-L polyethylene terephthalate (PET) containers belonging to three different water brands commercialized in Hungary were studied in order to determine their phthalate content by gas chromatography-mass spectrometry. Among the six investigated phthalates, diisobutyl phthalate, di-n-butyl-phthalate, benzyl-butyl phthalate and di(2-ethyl-hexyl) phthalate (DEHP) were determined in non-carbonated samples as follows: <3.0 ng L(-1)-0.2 μg L(-1), <6.6 ng L(-1)-0.8 μg L(-1), <6.0 ng L(-1)-0.1 μg L(-1) and <16.0 ng L(-1)-1.7 μg L(-1), respectively. Any of the above-mentioned phthalate esters could be detected in carbonated mineral water samples. DEHP was the most abundant phthalate in the investigated samples. It could be detected after 44 days of storage at 22 °C and its leaching was the most pronounced when samples were stored over 1200 days. Mineral water purchased in PET bottles of 0.5L had the highest phthalate concentrations compared to those obtained for waters of the identical brand bottled in 1.5-L or 2.0-L PET containers due to the higher surface/volume ratio. No clear trend could be established for phthalate leaching when water samples were kept at higher temperatures (max. 60 °C) showing improper storage conditions. Phthalate determination by pyrolysis-gas chromatography/mass spectrometric measurements in the plastic material as well as in the aqueous phase proved the importance of the quality of PET raw material used for the production of the pre-form (virgin vs. polymer containing recycled PET). PMID:23688967

  13. High performance protein microarrays based on glycidyl methacrylate-modified polyethylene terephthalate plastic substrate.

    PubMed

    Liu, Yingshuai; Li, Chang Ming; Hu, Weihua; Lu, Zhisong

    2009-01-15

    There is a great challenge to immobilize high density of probe molecules for high performance protein microarrays, and this is achieved in this work by using polyethylene terephthalate (PET) plastic substrate onto which glycidyl methacrylate (GMA) photopolymer is grafted under mild conditions to introduce high density of epoxy groups for covalent immobilization of proteins. The poly(GMA)-grafted PET (PGMA-PET) surface was characterized with atomic force microscope (AFM) and attenuated total reflectance Fourier transform infra-red (ATR-FTIR) spectroscopy. For high density of protein immobilization and good quality of microspots, experiments were conducted to optimize the printing buffer, and an optimal buffer was found out to be PBS with 10% glycerol+0.003% triton X-100. According to the studies of loading capacity and immobilization kinetics, the optimal protein probe concentration and incubation time for the efficient immobilization are 200 microg mL(-1) and 8h, respectively. The performance of the PGMA-PET-based protein microarrays is evaluated with sandwich immunoassay using rat IgG and anti-rat IgG as model proteins, demonstrating a limit of detection (LOD) of 10 pg mL(-1) and a dynamic range of five orders of magnitude which are better than or very comparable with the reported or commercially available immunoassays, while providing a high-throughput approach. The work renders a simple and economic method to manufacture high performance protein microarrays and is expected to have great potentials in broad applications related to clinic diagnosis, drug discovery and proteomic research. PMID:19064107

  14. Use of plastic waste (poly-ethylene terephthalate) in asphalt concrete mixture as aggregate replacement.

    PubMed

    Hassani, Abolfazl; Ganjidoust, Hossein; Maghanaki, Amir Abedin

    2005-08-01

    One of the environmental issues in most regions of Iran is the large number of bottles made from poly-ethylene terephthalate (PET) deposited in domestic wastes and landfills. Due to the high volume of these bottles, more than 1 million m3 landfill space is needed for disposal every year. The purpose of this experimental study was to investigate the possibility of using PET waste in asphalt concrete mixes as aggregate replacement (Plastiphalt) to reduce the environmental effects of PET disposal. For this purpose the mechanical properties of plastiphalt mixes were compared with control samples. This study focused on the parameters of Marshall stability, flow, Marshall quotient (stability-to-flow ratio) and density. The waste PET used in this study was in the form of granules of about 3 mm diameter which would replace (by volume) a portion of the mineral coarse aggregates of an equal size (2.36-4.75 mm). In all prepared mixes the determined 6.6% optimum bitumen content was used. In this investigation, five different percentages of coarse aggregate replacement were used. The results showed that the aggregate replacement of 20% by volume with PET granules would result in a reduction of 2.8% in bulk compacted mix density. The value of flow in the plastiphalt mix was lower than that of the control samples. The results also showed that when PET was used as partial aggregate replacement, the corresponding Marshall stability and Marshall quotient were almost the same as for the control samples. According to most of specification requirement, these results introduce an asphalt mix that has properties that makes it suitable for practical use and furthermore, the recycling of PET for asphalt concrete roads helps alleviate an environmental problem and saves energy. PMID:16200982

  15. Comparative assessment of genotoxicity of mineral water packed in polyethylene terephthalate (PET) and glass bottles.

    PubMed

    Ceretti, Elisabetta; Zani, Claudia; Zerbini, Ilaria; Guzzella, Licia; Scaglia, Mauro; Berna, Vanda; Donato, Francesco; Monarca, Silvano; Feretti, Donatella

    2010-03-01

    The potential migration of genotoxic compounds into mineral water stored in polyethylene terephthalate (PET) bottles was evaluated by an integrated chemical/biological approach using short-term toxicity/genotoxicity tests and chemical analysis. Six commercial brands of still and carbonated mineral water bottled in PET and in glass were stored at 40 degrees C for 10 days in a stove according to the standard EEC total migration test (82/711/EEC), or at room temperature in the dark. After treatment, the samples were analysed using gas-chromatography/mass spectrometry (GC/MS) to detect volatile and non-volatile compounds, the Microtox test to evaluate potential toxicity of the samples, and three mutagenicity tests -Tradescantia and Allium cepa micronucleus tests and the Comet assay on human leukocytes - to detect their genotoxic activity. GC/MS analysis did not detect phthalates or acetaldehyde in the water samples. The Microtox test found no toxic effects. Mutagenicity tests detected genotoxic properties of some samples in both PET and glass bottles. Statistical analyses showed a positive association between mineral content and mutagenicity (micronuclei in A. cepa and DNA damage in human leukocytes). No clear effect of treatment and PET bottle was found. These results suggest the absence of toxic compounds migrating from PET regardless of time and conditions of storage. In conclusion, bottle material and stove treatment were not associated with the genotoxic properties of the water; the genotoxic effects detected in bottled water may be related to the characteristics of the water (minerals and CO(2) content). PMID:19913274

  16. Contamination of bottled waters with antimony leaching from polyethylene terephthalate (PET) increases upon storage.

    PubMed

    Shotyk, William; Krachler, Michael

    2007-03-01

    Antimony concentrations were determined in 132 brands of bottled water from 28 countries. Two of the brands were at or above the maximum allowable Sb concentration for drinking water in Japan (2 microg/L). Elevated concentrations of Sb in bottled waters are due mainly to the Sb2O3 used as the catalyst in the manufacture of polyethylene terephthalate (PET(E)). The leaching of Sb from PET(E) bottles shows variable reactivity. In 14 brands of bottled water from Canada, Sb concentrations increased on average 19% during 6 months storage at room temperature, but 48 brands of water from 11 European countries increased on average 90% under identical conditions. A mineral water from France in PET(E), purchased in Germany, yielded 725 ng/L when first tested, but 1510 ng/L when it was stored for 6 months at room temperature; the same brand of water, purchased in Hong Kong, yielded 1990 ng/L Sb. Pristine groundwater containing 1.7+/-0.4 ng/L Sb (n = 6) yielded 26.6+/-2.3 ng/L Sb (n = 3) after storage in PET(E) bottles from Canada for 6 months versus 281+/-38 ng/L Sb (n = 3) in PET(E) bottles from Germany. Tap water bottled commercially in PET(E) in December 2005 contained 450+/-56 ng/L Sb (n = 3) versus 70.3+/-0.3 ng/L Sb (n = 3) when sampled from a household faucet in the same village (Bammental, Germany), and 25.7+/-1.5 ng/L Sb (n = 3) from a local artesian flow. PMID:17396641

  17. Polyethylene terephthalate membrane grafted with peptidomimetics: endothelial cell compatibility and retention under shear stress.

    PubMed

    Rémy, Murielle; Bareille, Reine; Rerat, Vincent; Bourget, Chantal; Marchand-Brynaert, Jacqueline; Bordenave, Laurence

    2013-01-01

    The present work aimed to treat a polyethylene terephthalate (PET) surface to make the biomaterial more 'attractive' in terms of attachment and shear stress response to endothelial cells with a view to possible applications in vascular grafting. A surface wet-chemistry protocol was applied to graft track-etched PET membranes with RGD peptidomimetics based on the tyrosine template and active at the nano-level vs. isolated human αvβ3 receptor, which was monitored by X-ray photoelectron spectroscopy, contact angle measurement and atomic force microscopy for characterization. A primary culture of human saphenous vein endothelial cells was used before and after sterilization of the membranes (heat treatment or γ-ray irradiation) to test the benefit of grafting. The optimal surface concentrations of grafted molecules were around 50 pmol/cm². Compared to GRGDS, the peptidomimetics promoted cell attachment with similar or slightly better performances. Endothelialized grafted supports were further exposed to 2 h of shear stress mimicking arterial conditions. Cells were lost on non-grafted PET whereas cells on grafted polymers sterilized by γ-ray irradiation withstood forces with no significant difference in focal contacts. At the mRNA level, cells on functionalized PET were able to respond to shear stress with NFkB upregulation. Thus, grafting of peptidomimetics as ligands of the αvβ3 integrin could be a relevant strategy to improve the adhesion of human endothelial cells and to obtain an efficient endothelialized PET for the surgery of small-diameter vascular prostheses. PMID:23565647

  18. Properties of poly(ethylene terephthalate) track membranes with a polymer layer obtained by plasma polymerization of pyrrole vapors

    NASA Astrophysics Data System (ADS)

    Kravets, L.; Dmitriev, S.; Lizunov, N.; Satulu, V.; Mitu, B.; Dinescu, G.

    2010-03-01

    The structure and the charge transport properties of poly(ethylene terephthalate) track membrane modified by pyrrole plasma were studied. It was found that polymer deposition on the surface of a track membrane via plasma polymerization of pyrrole results in the creation of composite nanomembranes that, in the case of the formation of a semipermeable layer, possess asymmetric conductivity in electrolyte solutions - a rectification effect similar to that of a p-n junction in semiconductors. It is caused by presence in the membranes of two layers with different functional groups and also by the pore geometry. Such membranes can be used to create chemical and biochemical sensors.

  19. Roles of inorganic oxide nanoparticles on extraction efficiency of electrospun polyethylene terephthalate nanocomposite as an unbreakable fiber coating.

    PubMed

    Bagheri, Habib; Roostaie, Ali

    2015-01-01

    In the present work, the roles of inorganic oxide nanoparticles on the extraction efficiency of polyethylene terephthalate-based nanocomposites were extensively studied. Four fiber coatings based on polyethylene terephthalate nanocomposites containing different types of nanoparticles along with a pristine polyethylene terephthalate polymer were conveniently electrospun on stainless steel wires. The applicability of new fiber coatings were examined by headspace-solid phase microextraction of some environmentally important volatile organic compound such as benzene, toluene, ethylbenzene and xylene (BTEX), as model compounds, from aqueous samples. Subsequently, the extracted analytes were transferred into a gas chromatography by thermal desorption. Parameters affecting the morphology and capability of the prepared nanocomposites including the type of nanoparticles and their doping levels along with the coating time were optimized. Four types of nanoparticles including Fe3O4, SiO2, CoO and NiO were examined as the doping agents and among them the presence of SiO2 in the prepared nanocomposite was prominent. The homogeneity and the porous surface structure of the SiO2-polyethylene terephthalate nanocomposite were confirmed by scanning electron microscopy indicating that the nanofibers diameters were lower than 300 nm. In addition, important parameters influencing the extraction and desorption process such as temperature and extraction time, ionic strength and desorption conditions were optimized. Eventually, the developed method was validated by gas chromatography-mass spectrometry. Under optimized conditions, the relative standard deviation values for a double distilled water spiked with the selected volatile organic compounds at 50 ng L(-1) were 2-7% (n=3) while the limits of detection were between 0.7 and 0.9 ng L(-1). The method was linear in the concentration range of 10 to 1,000 ng L(-1) (R(2)>0.9992). Finally, the developed method was applied to the analysis of

  20. Mechanical evaluation of newly developed mouthpiece using polyethylene terephthalate glycol for transoral robotic surgery.

    PubMed

    Fujiwara, Kazunori; Fukuhara, Takahiro; Niimi, Koji; Sato, Takahiro; Kataoka, Hideyuki; Kitano, Hiroya; Takeuchi, Hiromi

    2015-12-01

    Transoral robotic surgery (TORS), performed with the da Vinci surgical system (da Vinci), has been classified as a surgical approach for benign and malignant lesions of the oral cavity and laryngopharynx. It provides several unique advantages, which include a three-dimensional magnified view, ability to see and work around curves or angles, and the availability of two or three robotic arms. At present, however, the da Vinci surgical system does not provide haptic feedback. The potential risks specific to the transoral use of the da Vinci include tooth injury, mucosal laceration, ocular injury, and mandibular fracture. To prevent such intra-operative tooth injuries, we created a mouthpiece made of polyethylene terephthalate glycol (PETG) individually shaped for the patient's teeth. We compared the safety and efficacy of the PETG mouthpiece with those of a conventional mouthpiece made of ethylene-vinyl acetate (EVA). To determine the difference in tooth injury resulting from the two types of mouthpiece, we constructed an experimental system to measure load and strain. We measured the dynamic load and the strain from the rod to the tooth using the PETG and EVA mouthpiece. The rod was pressed against the tooth model outfitted with two types of mouthpiece and the dynamic load was measured with a load cell and the strain with a strain gage. The maximum dynamic load was 1.29 ± 0.03 kgf for the PETG mouthpiece and 2.24 ± 0.05 kgf for the EVA mouthpiece. The load against the tooth was thus less for the EVA mouthpiece. The strain was -166.84 ± 3.94 and 48.24 ± 7.77 με, respectively, while the load direction was parallel to that of the tooth axis for the PETG mouthpiece and perpendicular to the tooth axis for the EVA mouthpiece. The PETG mouthpiece reduced the tooth load compared with the EVA mouthpiece and the load direction was in parallel to the tooth axis. The PETG mouthpiece thus enhances tooth safety for TORS. PMID:26530849

  1. Analysis of the thermally stimulated discharge current around glass-rubber transition temperature in polyethylene terephthalate

    NASA Astrophysics Data System (ADS)

    Neagu, Eugen R.; Marat-Mendes, Jose N.; Das-Gupta, Dilip K.; Neagu, Rodica M.; Igreja, Rui

    1997-09-01

    The nature of the thermally stimulated discharge current (TSDC) for polyethylene terephthalate samples in the temperature range from room temperature to above glass-rubber transition temperature of the amorphous phase is analyzed. The well conditioning of the sample is strictly necessary in order to have a good reproducibility and accuracy of results. A main peak was observed whose maximum temperature moves towards a lower value with the decreasing of the amount of charge that flows through the sample during polarization. The peak position changes as well, if the sample is polarized in air or in oxygen and the nature of change is more important in the case of oxygen. The shape of the peak is complex and at least four shoulders have been identified around 85, 90, 105, and 125 °C using the cleaning technique. The activation energy tends to increase with repetition of the TSDC runs, in the glass-rubber transition temperature range, in the case when the cleaning technique is used for the peaks separation. For the conditioned samples, there is a good agreement between the experimental results and the analytical expression of the current, particularly in the region where it reaches a maximum, and so relevant values for the characteristic parameters of the peak are determined. The time interval of the short circuiting of the sample, at room temperature, before the TSDC measurement, strongly influences the initial rise of the current and consequently the parameters of the peak. A possible redistribution of the internal field arising from the injected charge, the heterocharge, and the existing charge in the sample as received, has been put forward to account for the experimental evidences. The conclusion is that the current is mainly determined by the space-charge released from the traps that are likely continuously distributed in energy. For the stated polarization conditions, the charge is released from the shallow traps with an activation energy in the range 0.23-0.32 e

  2. Water permeability of polyethylene terephthalate track membranes modified in plasma of dimethylaniline

    NASA Astrophysics Data System (ADS)

    Kravets, Lyubov; Dmitriev, Serguei; Gilman, Alla; Drachev, Alexander

    2004-09-01

    The surface properties and hydrodynamic characteristics of composite membranes consisting of a porous substrate, on which a polymer layer from a direct current discharge in a mixture of air and vapours of dimethylaniline was deposited, have been investigated. As a substrate, we used poly(ethylene) terephthalate track membrane (PET TM) of the thickness of 10 μ m and the effective pore diameter of 0.215 μ m (pore density is 2\\cdot 10^8 cm-2). The performed researches show that when treating the membranes in plasma, two competing processes are observed: deposition of the polymer layer on a membrane surface, that testifies increase of the mass of sample, and etching of a polymeric matrix which causes growth of effective pore diameter. The last process is stipulated by presence of oxygen in the gas mixture. Decreasing the degree of overweight of the sample at increasing the treatment time leads us to a supposition that a dominating process in this case becomes the process of gas-discharge etching. In all cases, if treating PET TM, a drop of the water contact angle occurs, i.e. hydrophilization of the membrane surface takes place that is connected first of all with a grafting of polymer layer containing polar functional groups. The research in the hydrodynamic characteristics of the initial PET TM and the membranes modified in plasma at neutral and subacid pH value of filtrate leads to a linear dependence of their permeability upon the quantity of applied pressure. It is connected with a viscous character of the flow, that is, when the diameter of the pores of the membrane is much more than the size of the water molecules. This fact shows that the macromolecules of the deposited polymer layer in this case have a compact conformation, which does not hinder the water molecules infiltration. At a lower pH value of the filtrate, the picture cardinally changes. For modified in plasma membranes a diversion from the linear relation is observed. This means that in this case

  3. Elastic and inelastic transmission of electrons through insulating polyethylene terephthalate nanocapillaries

    NASA Astrophysics Data System (ADS)

    Keerthisinghe, D.; Dassanayake, B. S.; Wickramarachchi, S. J.; Stolterfoht, N.; Tanis, J. A.

    2015-07-01

    The transmission of electrons with incident energies of 300, 500, and 800 eV through insulating polyethylene terephthalate (PET) nanocapillaries for small tilt angles near 0° was studied. The exiting electrons showed elastic and inelastic behaviors with the inelasticity increasing with the tilt angle. This paper is an extension of our earlier work for electrons on PET reported by Das et al. [Phys. Rev. A 76, 042716 (2007), 10.1103/PhysRevA.76.042716], but the present study goes further by investigating the transmission for very small tilt angles near 0° with the small step sizes revealing distinct regions of behavior. The work performed here was conducted for two samples with different capillary diameters and pore densities: sample 1 with 100-nm diameter capillaries in a foil of 12-µm thickness and a pore density of 5 ×108/cm2 , and sample 2 with 200-nm diameter capillaries with the same foil thickness and a pore density of 5 ×107/cm2 . Two distinct regions of transmission depending on the sample tilt angle for both samples corresponding to direct and guided electrons as well as the transition region between them were observed. The angular centers and widths of the transmission for each angle investigated were found and are discussed in terms of the tilt angle variation in the foil. For the widths, comparison with the inherent angular width of the electron spectrometer is made. Energy loss of electrons was studied from the centroids of the energy spectra with these energies corresponding to the peak centers of the angular profiles. The broadness of the energy distributions due to inelasticity was investigated from the full width at half maxima (in eV) of the spectra. The results for both samples agreed well despite the differences in capillary diameters and pore densities. The results are in partial agreement with the previous work performed for PET nanocapillaries by Das et al. [Phys. Rev. A 76, 042716 (2007), 10.1103/PhysRevA.76.042716], but differences are

  4. FTIR analysis of polyethylene terephthalate irradiated by MeV He+

    NASA Astrophysics Data System (ADS)

    Djebara, M.; Stoquert, J. P.; Abdesselam, M.; Muller, D.; Chami, A. C.

    2012-03-01

    The degradation induced by MeV He+ ions onto polyethylene terephthalate (PET) is investigated as a function of fluence and electronic stopping power (dE/dx)e. Stack samples of four 3.6 μm PET films are irradiated by 3.5 MeV He+ under vacuum and room temperature at fluence ranging from 1013 to 1.5 × 1015 He+ cm-2. The entrance energies range from 3.5 MeV for the front film to 0.573 MeV for the rear one at the beginning of the irradiation and the corresponding mean (dE/dx)e lie for pristine PET between 158 and 264 keV/μm. A Fourier transform infrared spectroscopy (FTIR) analysis is undertaken. The different stack films present similar damages with magnitude increase as the fluence goes up. Moreover, higher is the electronic stopping power (dE/dx)e more important is the damage. The evolution of the normalized integrated absorbance A(ϕ)/A0 of the internal reference 1410 cm-1 band as a function of the fluence ϕ presents a complex behavior characterized by a two-exponential decay associated to low and high fluence range. The analysis reveals clearly that the A(ϕ)/A0 of the characteristic benzene ring 1577 cm-1 band remains steady till fluence around 3 × 1014 He+ cm-2 and then decreases smoothly as fluence increases. The band appearing at 1610 cm-1, assigned to mono substituted benzene, presents an integrated absorbance A(ϕ) which rises progressively and levels off beyond a critical fluence around 4 × 1014 He+ cm-2. The cross section of the creation of the monosubstituted benzene lies between 3 × 10-15 and 6 × 10-15 cm2 for (dE/dx)e = 158 and 264 keV/μm, respectively. Drastic loss of crystallinity is induced by the MeV He+ ion irradiation in the polymer. The amorphization is monitored by the evolution of the specific bands of the trans and gauche ethylene glycol residue conformations. A sudden drop in the integrated absorbance of the 1340 cm-1 band which characterizes the trans conformation is observed at fluence around 2 × 1014 He+ cm-2. On the other hand, a

  5. 76 FR 47558 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-05

    ...) Resin From India, 70 FR 13460 (March 21, 2005), and accompanying Issues and Decision Memorandum at... Terephthalate Film, Sheet, and Strip (PET Film) from India, 67 FR 44179 (July 1, 2002). On July 1, 2010, the... Administrative Review, 75 FR 38074 (July 1, 2010). The Department received a request for review from...

  6. 76 FR 18519 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Amended Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-04

    ... Terephthalate Film, Sheet, and Strip From Taiwan: Final Results of Antidumping Duty Administrative Review, 76 FR... Proceedings: Assessment of Antidumping Duties, 68 FR 23954 (May 6, 2003). This clarification applies to... Taiwan, 67 FR 44174 (July 1, 2002), as corrected in 67 FR 46566 (July 15, 2002). Cash...

  7. 76 FR 76941 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-09

    ..., Sheet, and Strip From Taiwan: Preliminary Results of Antidumping Duty Administrative Review, 76 FR 47540... Proceedings: Assessment of Antidumping Duties, 68 FR 23954 (May 6, 2003). \\13\\ See Notice of Amended Final... Terephthalate Film, Sheet, and Strip (PET Film) from Taiwan, 67 FR 44174 (July 1, 2002) (Investigation...

  8. Rheological characterization of degradation and polycondensation of poly(ethylene terephthalate) melt in air and in nitrogen

    NASA Astrophysics Data System (ADS)

    Kruse, Matthias; Rolón-Garrido, Víctor H.; Wagner, Manfred H.

    2013-04-01

    Three different poly(ethylene terephthalate) (PET) samples based on dimethyl terephthalate or terephthalic acid, were studied in terms of alterations and mutations caused by thermal exposure during rheological characterization. Thermal stability and frequency sweep experiments were performed in the melt state at a temperature of 280°C, and the influence of the atmosphere (air or nitrogen) as well as the effect of sample preparation (pellets molten directly between the plates of the rheometer vs. samples cut from compression molded sheets) were studied. Thermal stability tests reveal a fundamentally different behavior of the storage (G') and the loss (G″) modulus for measurements in air compared to measurements in a pure nitrogen atmosphere. Samples measured in air show a decrease of both moduli due to thermal degradation, while an unexpected strong increase was observed in nitrogen due to polycondensation. The loading time of the samples caused already a significant change of the rheological properties, which could be reconstructed by extrapolation to zero loading time. Frequency sweep test were significantly affected by the rapid changes of the molecular structure. Frequency sweeps were conducted bidirectional, i.e. by first increasing the angular frequency from 0.05 rad.s-1 to 500 rad.s-1, which was then followed by a decrease from 500 rad.s-1 to 0.05 rad.s-1, and vice versa. These tests confirm the effects of the atmosphere applied, air or nitrogen, causing degradation and condensation, respectively. However, besides these dominating alterations, i.e. reduction of the molecular weight due to chain scission in air and increase of the molecular weight due to condensation reactions in nitrogen, also the opposite effects were detected. This indicates clearly the formation of a bimodal molecular weight distribution whose existence was supported by the rheological characterization of compression molded plates, which were found to show more degradation but also

  9. Bilayered biodegradable poly(ethylene glycol)/poly(butylene terephthalate) copolymer (Polyactive) as substrate for human fibroblasts and keratinocytes.

    PubMed

    van Dorp, A G; Verhoeven, M C; Koerten, H K; van Blitterswijk, C A; Ponec, M

    1999-12-01

    The purpose of this study was to find an optimal polymer matrix and to optimize the culture conditions for human keratinocytes and fibroblasts for the development of a human skin substitute. For this purpose porous, dense bilayers made of a block copolymer of poly(ethylene glycol terephthalate) (PEGT) and poly(butylene terephthalate) (PBT; Polyactivetrade mark) with a PEGT/PBT weight ratio of 55/45 and a PEG molecular weight (MW) of 300, 600, 1000, or 4000 Da were used. The best performance was achieved with PEGT/PBT copolymer with MW of PEG 300 D (300PEG55PBT45). When fibroblasts were seeded into the porous underlayer and cultured for 3 weeks in medium supplemented with 100 microg/mL ascorbic acid, all pores were filled with fibroblasts and with extracellular matrix, which was judged from the presence of collagen types I, III, and IV, and laminin. When seeded onto the dense top layer of the bilayered (cell free or fibroblast populated) copolymer matrix, human keratinocytes grew out into confluent sheets. After subsequent lifting to the air-liquid interface, a multilayered epithelium with a morphology corresponding to that of the native epidermis was formed. Some differences could still be observed: the expression and localization of some differentiation specific proteins was different and close to that seen in hyperproliferative epidermis; a basal lamina and anchoring zone were absent. PMID:10487879

  10. A dual enzyme system composed of a polyester hydrolase and a carboxylesterase enhances the biocatalytic degradation of polyethylene terephthalate films.

    PubMed

    Barth, Markus; Honak, Annett; Oeser, Thorsten; Wei, Ren; Belisário-Ferrari, Matheus R; Then, Johannes; Schmidt, Juliane; Zimmermann, Wolfgang

    2016-08-01

    TfCut2 from Thermobifida fusca KW3 and the metagenome-derived LC-cutinase are bacterial polyester hydrolases capable of efficiently degrading polyethylene terephthalate (PET) films. Since the enzymatic PET hydrolysis is inhibited by the degradation intermediate mono-(2-hydroxyethyl) terephthalate (MHET), a dual enzyme system consisting of a polyester hydrolase and the immobilized carboxylesterase TfCa from Thermobifida fusca KW3 was employed for the hydrolysis of PET films at 60°C. HPLC analysis of the reaction products obtained after 24 h of hydrolysis showed an increased amount of soluble products with a lower proportion of MHET in the presence of the immobilized TfCa. The results indicated a continuous hydrolysis of the inhibitory MHET by the immobilized TfCa and demonstrated its advantage as a second biocatalyst in combination with a polyester hydrolase for an efficient degradation oft PET films. The dual enzyme system with LC-cutinase produced a 2.4-fold higher amount of degradation products compared to TfCut2 after a reaction time of 24 h confirming the superior activity of his polyester hydrolase against PET films. PMID:27214855

  11. Guiding of slow Ne{sup 7+} ions through nanocapillaries in insulating polyethylene terephthalate: Incident current dependence

    SciTech Connect

    Stolterfoht, N.; Hellhammer, R.; Bundesmann, J.; Fink, D.; Kanai, Y.; Kambara, T.; Ikeda, T.; Hoshino, M.; Yamazaki, Y.

    2007-08-15

    The transmission of highly charged ions through nanocapillaries in insulating polyethylene terephthalate (PET) polymers was investigated. In experiments at laboratories in RIKEN (Japan) and HMI (Germany) different detection methods were applied to study the ion current dependence in a wide range covering two orders of magnitude. At HMI an electrostatic ion spectrometer was used and at RIKEN a two-dimensional position sensitive detector was implemented. New PET samples with parallel capillaries and low density were manufactured. For tilted capillaries, the ions are guided along the capillary axis, since the majority of ions are deflected in a charge patch created in the capillary entrance. The results provide insights into the mechanisms of capillary guiding. The fraction of transmitted ions was found to be nearly independent on the incident ion current indicating a sudden increase in the discharge current depleting the entrance charge patch. The experimental results were well-reproduced by model calculations based on a nonlinear (exponential) expression for the discharge current.

  12. Improvement of Permeation of Solvent-Free Multilayer Encapsulation of Thin Films on Poly(ethylene terephthalate)

    NASA Astrophysics Data System (ADS)

    Han, Jin-Woo; Kang, Hee-Jin; Kim, Jong-Yeon; Kim, Gwi-Yeol; Seo, Dae-Shik

    2006-12-01

    In this study, inorganic multilayer thin-film encapsulation is adopted for the first time to protect an organic layer from moisture and oxygen. Inorganic multilayer thin-film encapsulation is deposited onto poly(ethylene terephthalate) (PET) using an electron beam and sputtering. The SiON/SiO2 and parylene layer show the most suitable properties. Under these conditions, the water vapor transmission rate (WVTR) for PET can be reduced from a level of 0.57 g m-2 day-1 (bare substrate) to 1× 10-5 g m-2 day-1 after the application of a SiON and SiO2 layer. These results indicate that PET/parylene/SiO2/SiON barrier coatings have high potential for flexible organic light-emitting diode (OLED) applications.

  13. Tailoring the Properties of Poly(ethylene terephthalate) without Addition of Fillers via Solid-State Shear Pulverization

    NASA Astrophysics Data System (ADS)

    Pierre, Cynthia; Kasimatis, Kosmas; Torkelson, John

    2008-03-01

    We demonstrate the ability to very strongly tune the physical and mechanical properties of poly(ethylene terephthalate) (PET) by changing the processing conditions of neat PET during solid-state shear pulverization without addition of any fillers or nucleating agents. Using differential scanning calorimetry, we observe a roughly factor of 3 increase in crystallinity of PET that has been pulverized and subsequently melted relative to the unprocessed PET. We also observe a dramatic increase in the rate of crystallization of the pulverized samples. Rheological characterization has demonstrated an increase in viscosity of the pulverized material, which can be ascribed to chain branching in the pulverized product. We also observe significant reductions in the oxygen permeability of the PET with pulverization as well as enhancements in mechanical properties that are commensurate with the modified crystallization properties of the pulverized PET.

  14. Pretreatment of polyethylene terephthalate substrate for the growth of Ga-doped ZnO thin film.

    PubMed

    Kim, D W; Kang, J H; Lim, Y S; Lee, M H; Seo, W S; Park, H H; Seo, K H; Park, M G

    2011-02-01

    The effect of the pretreatment of polyethylene terephthalate (PET) substrate on the growth of transparent conducting Ga-doped ZnO (GZO) thin film was investigated. Because of its high gas and moisture absorption and easy gas permeation, PET substrate was annealed at 100 degrees C in a vacuum chamber prior to the sputtering growth of GZO thin film for the outgassing of impurity gases. GZO thin film was deposited on the pretreated PET substrate by rf-magnetron sputtering and significantly improved electrical properties of GZO thin film was achieved. Electrical and structural characterizations of the GZO thin films were carried out by 4-point probe, Hall measurement, and scanning electron microscopy, and the effects of the pretreatment on the improved properties of GZO thin films were discussed. This result is not only useful to PET substrate, but also could be applicable to other plastic substrates which inevitably containing the moisture and impurity gases. PMID:21456250

  15. Treatment of poly(ethylene terephthalate) foils by atmospheric pressure air dielectric barrier discharge and its influence on cell growth

    NASA Astrophysics Data System (ADS)

    Kuzminova, Anna; Vandrovcová, Marta; Shelemin, Artem; Kylián, Ondřej; Choukourov, Andrei; Hanuš, Jan; Bačáková, Lucie; Slavínská, Danka; Biederman, Hynek

    2015-12-01

    In this contribution an effect of dielectric barrier discharge (DBD) sustained in air at atmospheric pressure on surface properties of poly(ethylene terephthalate) (PET) foils is studied. It is found that exposure of PET to DBD plasma leads to rapid changes of surface chemical composition, wettability, surface morphology as well as mechanical properties of PET surface. In addition, based on biological tests that were performed using two cell types (Saos-2 human osteoblast-like cells and HUVEC human umbilical vein endothelial cells), it may be concluded that DBD plasma treatment positively influences cell growth on PET. This effect was found to be connected predominantly with increased surface energy and oxygen content of the surface of treated PET foils.

  16. Construction of antibacterial poly(ethylene terephthalate) films via layer by layer assembly of chitosan and hyaluronic acid.

    PubMed

    Del Hoyo-Gallego, Sara; Pérez-Álvarez, Leyre; Gómez-Galván, Flor; Lizundia, Erlantz; Kuritka, Ivo; Sedlarik, Vladimir; Laza, Jose Manuel; Vila-Vilela, Jose Luis

    2016-06-01

    Polyelectrolytic multilayers (PEMs) with enhanced antibacterial properties were built up onto commercial poly(ethylene terephthalate) (PET) films based on the layer by layer assembling of bacterial contact killing chitosan and bacterial repelling highly hydrated hyaluronic acid. The optimization of the aminolysis modification reaction of PET was carried out by the study of the mechanical properties and the surface characterization of the modified polymers. The layer by layer assembly was successfully monitored by TEM microscopy, surface zeta-potential, contact angle measurements and, after labeling with fluorescein isothiocyanate (FTIC) by absorption spectroscopy and confocal fluorescent microscopy. Beside, the stability of the PEMs was studied at physiological conditions in absence and in the presence of lysozyme and hyaluronidase enzymes. Antibacterial properties of the obtained PEMs against Escherichia coli were compared with original commercial PET. PMID:27083341

  17. Effect of supercritical carbon dioxide as an exfoliation aid on bio-based polyethylene terephthalate glycol-modified/clay nanocomposites

    NASA Astrophysics Data System (ADS)

    Jang, Kwangho; Lee, Jae Wook; Hong, In-Kwon; Lee, Sangmook

    2013-08-01

    Bio-based PETG (bio-based glycol modified polyethylene terephthalate, Ecozen T95) / clay (organo-modified montmorillonite, OMMT, C10A) nanocomposites were prepared by co-rotating twin screw extruder attached with supercritical carbon dioxide (scCO2) injection system. The effects of nano-clay and scCO2 on the properties of PETG/clay nanocomposites were investigated by measuring thermal, rheological, tensile, impact, and barrier properties. The thermal and mechanical properties decreased with increasing nano-clay content, but they recovered or even exceeded the properties of neat PETG as scCO2 was added. It was verified due to a good dispersion of the nano-clay in PETG matrix for PETG/clay nanocomposites by XRD, SEM, and TEM. It was thought that scCO2 could be an effective exfoliation agent for many nanocomposites systems as well as for bio-based PET/clay nanocomposites.

  18. The effect of local fluence on the micropatterning of poly(ethylene terephthalate) foils through proton beam writing

    NASA Astrophysics Data System (ADS)

    de Souza, C. T.; Stori, E. M.; Boufleur, L. A.; Papaléo, R. M.; Dias, J. F.

    2016-07-01

    In this work, we investigate the influence of ion fluence on the development of microstructures produced by 2.2 MeV H+ impinging on 12-μm-thick poly(ethylene terephthalate) (PET, Mylar®) foils. Several lines of 1 × 100 pixels corresponding to approximately 2.5 × 101.5 µm2 were patterned on PET foils using different ion fluences (from 1012 to 1017 H+/cm2) and etching times (from 1 to 60 min). We observe the presence of three different behaviors according to the ion fluence. Long etching times are necessary to open the structure in the low fluence regime, while moderate fluences require shorter etching times. In the high fluence regime, a more complex scenario emerges where short etching times lead to structures either fully or partially developed.

  19. Micromechanical modelling of short-term and long-term large-strain behaviour of polyethylene terephthalate

    NASA Astrophysics Data System (ADS)

    Poluektov, M.; van Dommelen, J. A. W.; Govaert, L. E.; Yakimets, I.; Geers, M. G. D.

    2013-12-01

    A micromechanically based model is used to describe the mechanical behaviour of polyethylene terephthalate (PET) under uniaxial compression up to large strains and at different temperatures. The creep behaviour of isotropic PET is simulated and compared to experimental data to demonstrate the applicability of the model to describe the long-term response. The material is modelled as an aggregate of two-phase layered domains, where different constitutive laws are used for the phases. A hybrid interaction law between the domains is adopted. The crystalline phase is modelled with crystal plasticity and the amorphous phase with the Eindhoven Glassy Polymer model, taking into account material ageing effects. Model parameters for the selected constitutive laws of the phases are identified from uniaxial compression tests for fully amorphous material and semicrystalline material. Texture evolution during the deformation predicted by the model adequately matches previously observed texture evolution.

  20. Design and synthesis of comonomers to enhance the optical, physical, and thermal properties of poly(ethylene terephthalate)

    NASA Astrophysics Data System (ADS)

    Connor, Daniel Martin

    Poly(ethylene terephthalate) (PET) is one of the world's most important commodity plastics. The largest volume applications of PET include textile fiber, tire cord, and packaging materials. There are many opportunities for improving the properties of PET that are associated with its various applications. We address three of the major application driven issues in PET: Increasing the optical brightness, increasing the crystallization rate, and enhancing the optical clarity through inhibition of crystallization. Each of the projects is summarized below. A new class of monomeric fused aromatic fluorescent brightening agents based on pyrene and anthracene have been designed and synthesized. The monomers: dimethyl 1,6-pyrene dicarboxylate, dimethyl 1,8-pyrenedicarboxylate, dimethyl 2,7-pyrenedicarboxylate, 1,9-bis(2-carboxybenzoyl)pyrene dimethyl ester, dimethyl 2,6-anthracenedicarboxylate, dimethyl 2,7-anthracenedicarboxylate and dimethyl 9,10-anthracenedicarboxylate were copolymerized with poly(ethylene terephthalate) and their optical properties were assessed. All of the polymers gave blue fluorescence with the copolymer containing dimethyl 1,6-pyrenedicarboxylate being the brightest. The synthesis of 2,7-substituted pyrene derivatives needed for the optical brightening project and for the crystallization rate enhancement project posed unique challenges. Optimized synthetic procedures for these compounds were developed. Pyrenes derivatized in the 2- and 7-positions were prepared by reduction of pyrene to 4,5,9,10-tetrahydropyrene followed by electrophilic aromatic substitution and re-aromatization. An optimized procedure is presented for hydrogenation of pyrene to provide 4,5,9,10-tetrahydropyene in high yield, which facilitates a convenient synthesis of dimethyl 2,7-pyrenedicarboxylate.

  1. Approaches toward high oxygen barrier poly(ethylene terephthalate) and preparation of di-isocyanate infused clay aerogel composites

    NASA Astrophysics Data System (ADS)

    Somlai, Louis Steven

    The first part of this dissertation discusses the synthesis and characterization of new poly(ethylene terephthalate) (PET) copolymers produced with 5-adamantylisophthalic acid monomer. Both monomer and copolymer syntheses are given in detail. Differential scanning calorimetry analyses of copolymers showed decreased melt transition temperatures with increased comonomer incorporation (0 to 5 mol-%), while copolymer glass transition temperatures increased slightly. Oxygen permeability was shown to increase with higher 5-adamantylisophthalic acid incorporation in the copolymers relative to virgin PET. The second part of this dissertation discusses PET-montmorillonite clay layered nanocomposites. Most commercially available, organically modified clays (OMCs) do not exhibit sufficient thermal stability for processing in commodity polymers such as poly(ethylene terephthalate). Surfactant degradation often leads to polymer discoloration and may be partially responsible for incomplete dispersion of the OMCs into PET. Our goal was to study the thermal stability of 4-(dimethylamino)pyridinium and 1,2-dimethylimidazolium surfactants, with a variety of long aliphatic hydrocarbon based tails on sodium exchanged montmorillonite, laponite, and fluoromica. Surfactant-sodium ion exchange resulted in increased onset of mass loss (OML) temperatures for surfactants on clays. Solvent extraction of unbound surfactant from OMC and lower percent surfactant-sodium ion exchange resulted in increased OML temperatures. Clay substrate also affects the OML temperature and mass loss profile. Preliminary experiments with these new OMCs and PET, at low incorporation via autoclave polymerization and melt-mixing, showed limited dispersion of silicate layers into the PET matrix and negligible changes to polymer thermal properties. The final part of this dissertation discusses diisocyanate infused montmorillonite aerogel composites. A process for the conversion of clay powder to organically modified

  2. Chitosan/poly (vinyl pyrollidone) coatings improve the antibacterial properties of poly(ethylene terephthalate)

    NASA Astrophysics Data System (ADS)

    Wang, Bai-liang; Wang, Jin-lei; Li, Dan-dan; Ren, Ke-feng; Ji, Jian

    2012-08-01

    Chitosan/poly (vinyl pyrollidone) (CHI/PVP) coatings were prepared to improve the antibacterial properties of poly (ethylene terephthalate) (PET) by a simple dip-coating method. The binding capability of CHI/PVP coatings was enhanced by successively pretreatment of PET by polyetherimide and polyacrylic acid and crosslinking. Measurements of water contact angle and atomic force microscope revealed that the coatings created a highly hydrophilic surface with low roughness. Adherences of Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) on PET with CHI/PVP coating were significantly reduced. Bactericidal activity of CHI/PVP coatings was good against E. coli and S. aureus and the adding of PVP obviously increased its antiadhesion property. In vitro cytotoxicity tests, cell morphology and activity evaluation of human umbilical vein endothelial cells showed that CHI/PVP coatings had good biocompatibility.

  3. Surface treatment of poly(ethylene terephthalate) by gamma-ray induced graft copolymerization of methyl acrylate and its toughening effect on poly(ethylene terephthalate)/elastomer blend

    NASA Astrophysics Data System (ADS)

    Ma, Liang; Wang, Mozhen; Ge, Xuewu

    2013-09-01

    To improve the compatibility between ethylene-methyl acrylate-glycidyl methacrylate random terpolymer (E-MA-GMA) elastomer and poly(ethylene terephthalate) (PET), thereby enhance the toughening effect of E-MA-GMA on PET, γ-radiation-induced graft copolymerization technique was used to graft methyl acrylate (MA) monomer onto PET. The produced PET-g-PMA copolymer can be used as a self-compatibilizer in PET/E-MA-GMA blend since the copolymer contains the same segments, respectively, with PET and E-MA-GMA. The impact strength of PET/E-MA-GMA blend increased nearly by 30% in the presence of less than 0.1 wt% PET-g-PMA compared with that of the neat PET/elastomer blend, without loss of the tensile strength of the blends. This work proposed a potential application of radiation-induced grafting copolymerization technique on the in-situ compatibilization of PET/elastomer blends so as to improve the integral mechanical properties of PET based engineering plastic.

  4. Effects of L-arginine immobilization on the anticoagulant activity and hemolytic property of polyethylene terephthalate films

    NASA Astrophysics Data System (ADS)

    Liu, Yun; Yang, Yun; Wu, Feng

    2010-04-01

    Surface modification of polyethylene terephthalate (PET) films was performed with L-arginine ( L-Arg) to gain an improved anticoagulant surface. The surface chemistry changes of modified films were characterized by X-ray photoelectron spectroscopy (XPS) and attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy. The in vitro anticoagulant activities of the surface-modified PET films were evaluated by blood clotting test, hemolytic test, and the measurement of clotting time including plasma recalcification time (PRT), activated partial thromboplastin time (APTT), and prothrombin time (PT). The data of blood coagulation index (BCI) for L-arginine modified PET films (PET-Arg) was larger than that for PET at the same blood-sample contact time. The hemolysis ratio for PET-Arg was less than that for PET and within the accepted standard for biomaterials. The PRT and APTT for PET-Arg were significantly prolonged by 189 s and 25 s, respectively, compared to those for the unmodified PET. All results suggested that the currently described modification method could be a possible candidate to create antithrombogenic PET surfaces which would be useful for further medical applications.

  5. Two-wavelength Raman study of poly(ethylene terephthalate) surfaces modified by helium plasma-based ion implantation

    NASA Astrophysics Data System (ADS)

    Veres, M.; Tóth, A.; Mohai, M.; Bertóti, I.; Szépvölgyi, J.; Tóth, S.; Himics, L.; Koós, M.

    2012-12-01

    The surface of poly(ethylene terephthalate) (PET) was modified by helium plasma-based ion implantation (He PBII). The untreated and surface modified samples were characterised with optical absorption spectroscopy and two-wavelength micro-Raman spectroscopy excited with 488 nm and 785 nm light sources, allowing to examine the chemical bonding configuration of the surface layers on different depths and by selective enhancement of vibrations of different structural units. Upon treatment, simultaneously with the development of the broad D and G bands, a gradual decrease of the peaks corresponding to the Cdbnd C stretching and Cdbnd O stretching modes were observed with both excitations. Downshifting and broadening were detected for the Cdbnd C peak with both excitations and also for the Cdbnd O peak with the 488 nm excitation due to formation of condensed aromatic rings. Oppositely, upshifting was found with 785 nm excitation for the Cdbnd O peak and especially for its broad shoulder newly developed at the high wavenumber side. The latter feature was assigned to Cdbnd O groups attached to polymer chains without conjugation and the bands behaviour was interpreted by breaking of the Cdbnd C bonds of the polymer, leading to the formation of a crosslinked, disordered and stressed structure with still intact Cdbnd O groups, due to the increased nuclear damage at the end of the ion track.

  6. Contaminants and levels of occurrence in washed and shredded poly(ethylene terephthalate) from curbside collection. Part 1: Extraction conditions.

    PubMed

    Konkol, L M; Cross, R F; Harding, I H; Kosior, E

    2003-09-01

    The aim was to determine which contaminants were present in washed and dried shredded poly(ethylene terephthalate) (PET, flake) obtained from curbside collection and whether the concentrations were above the US FDA threshold of 215 ppb. Thirty-two semi-volatile contaminants were extracted from the treated flake by Soxhlet extraction using dichloromethane as a PET swelling solvent and gas chromatography-mass spectrometry (GC-MS) was used for identification and quantification. Soxhlet extraction of flake ground to 0-300 pm was effectively completed in 24 h, whereas sonication reduced the extraction time to 3 h. In contrast, Soxhlet extractions of flake ground to a larger particle size range (300-425 pm) were completed in 4 h, possibly due to less aggregation in the extraction thimble. The levels of 26 contaminants were below 215 ppb, but six were not. Dodecanoic acid was present at about 1200 ppb, 2-butoxyethanol was approximately 1000 ppb, limonene, benzophenone and methyl salicylate were above 800 ppb, and 2-methyl-naphthalene near 215 ppb. PMID:13129782

  7. Fracture mechanism of metal electrode integrated on a chip and fabrication of a poly(ethylene terephthalate) electrophoresis microchip.

    PubMed

    Liu, Chong; Li, Jing-Min; Liu, Jun-Shan; Wang, Li-Ding; Hao, Zhen-Xia; Chen, Heng-Wu

    2009-10-15

    Thermal bonding is an important technique to fabricate polymer electrophoresis microchip. However, the metal electrodes deposited on polymer substrate can readily fracture during the thermal bonding. In this paper, poly(ethylene terephthalate) (PET) was exploited to fabricate the electrophoresis microchip with an integrated gold electrode for amperometric detection. The fracture of the gold electrode was studied through FEA (finite element analysis) simulations, the potentially risk positions on the electrode were shown. The calculation results were tested by bonding experiments and were proven to be consistent with the experiments. Besides, an optimal bonding temperature for PET chip was also presented based on FEA simulations and bonding experiments. Considering the low surface properties of PET, oxygen plasma-assisted thermal bonding technique was used to enhance bonding. Upon treated for 150 s, the PET substrates could be thermally bonded at 62 degrees C without electrode fracture. The fabricated PET chips were demonstrated for detection of standard glucose solution. Satisfactory reproducibility was achieved, and the RSD values of peak height and migration time of the PET CE chips were 0.51% and 2.17%, respectively. PMID:19635368

  8. Biotin-functionalized poly(ethylene terephthalate) capillary-channeled polymer fibers as HPLC stationary phase for affinity chromatography.

    PubMed

    Jiang, Liuwei; Marcus, R Kenneth

    2015-01-01

    Native poly(ethylene terephthalate) (PET) capillary-channeled polymer (C-CP) fibers have been used as the stationary phase for high-performance liquid chromatography (HPLC) of proteins via reversed-phase and ion-exchange processes. Functionalization can be used to bring about greater selectivity through surface modification. PET fibers were treated with ethylenediamine to generate primary amine groups on the fiber surface, enabling subsequent covalent attachment of ligands. The ninhydrin test for primary amines revealed surface densities of 13.9-60.0 μmol m(-2) for PET fibers exposed for periods of 3-12 min. Here, 8-amino-3,6-dioxaoctanoic acid was linked to the EDA-treated PET fiber surface as a hydrophilic spacer, and then D-biotin was attached on the end of the spacer as an affinity ligand. The streptavidin binding capacity and binding homogeneity were studied on the biotin-functionalized PET C-CP fiber microbore column. The selectivity of the biotin surface functionalization was assessed by spiking lysate with Texas Red-labeled streptavidin and enhanced green fluorescent protein. Greater than 99% selectivity was realized. This ligand-coupling strategy from standard solid-phase peptide synthesis used in stationary phase functionalization creates great potential for PET C-CP fiber-packed HPLC columns to perform a variety of chromatographic separations. PMID:25410640

  9. Stepwise crystallization and the layered distribution in crystallization kinetics of ultra-thin poly(ethylene terephthalate) film.

    PubMed

    Zuo, Biao; Xu, Jianquan; Sun, Shuzheng; Liu, Yue; Yang, Juping; Zhang, Li; Wang, Xinping

    2016-06-21

    Crystallization is an important property of polymeric materials. In conventional viewpoint, the transformation of disordered chains into crystals is usually a spatially homogeneous process (i.e., it occurs simultaneously throughout the sample), that is, the crystallization rate at each local position within the sample is almost the same. Here, we show that crystallization of ultra-thin poly(ethylene terephthalate) (PET) films can occur in the heterogeneous way, exhibiting a stepwise crystallization process. We found that the layered distribution of glass transition dynamics of thin film modifies the corresponding crystallization behavior, giving rise to the layered distribution of the crystallization kinetics of PET films, with an 11-nm-thick surface layer having faster crystallization rate and the underlying layer showing bulk-like behavior. The layered distribution in crystallization kinetics results in a particular stepwise crystallization behavior during heating the sample, with the two cold-crystallization temperatures separated by up to 20 K. Meanwhile, interfacial interaction is crucial for the occurrence of the heterogeneous crystallization, as the thin film crystallizes simultaneously if the interfacial interaction is relatively strong. We anticipate that this mechanism of stepwise crystallization of thin polymeric films will allow new insight into the chain organization in confined environments and permit independent manipulation of localized properties of nanomaterials. PMID:27334189

  10. Assessing human exposure to phthalic acid and phthalate esters from mineral water stored in polyethylene terephthalate and glass bottles.

    PubMed

    Montuori, P; Jover, E; Morgantini, M; Bayona, J M; Triassi, M

    2008-04-01

    Phthalic acid and phthalate esters are of growing interest due to their significant usage and potential toxicity. Polyethylene terephthalate (PET) and glass are both widely used materials for bottled drinking water. In this study, phthalic acid (PhA), bis(2-ethylhexyl) phthalate (DEHP), dimethyl phthalate (DMP), diethyl phthalate (DEP), diisobutyl phthalate (DiisoBP) and dibutyl phthalate (DBP) were analysed in a large number of Italian bottled water samples. These samples showed different concentrations of phthalates are nearly 20 times higher in samples bottled in PET than those from glass bottles with total levels of phthalates of 3.52 and 0.19 microg l(-1), respectively. However, the observed levels do not represent a significant exposure pathway when considering the US Environmental Protection Agency (USEPA) reference dose (an estimate of a daily oral exposure to the human population, including sensitive subgroups, that is likely to be without an appreciable risk of deleterious effects during a lifetime). In addition, no significant correlation was found between the phthalate concentrations and the physicochemical properties of the different water samples, apart from the still/sparkling water parameter for the PET samples. In this instance, slightly higher concentrations were observed for the PET bottled still water samples than for the sparkling water samples, although no explanation has been found yet. PMID:18348049

  11. Flat-pressed wood plastic composites from sawdust and recycled polyethylene terephthalate (PET): physical and mechanical properties.

    PubMed

    Rahman, Khandkar-Siddikur; Islam, Md Nazrul; Rahman, Md Mushfiqur; Hannan, Md Obaidullah; Dungani, Rudi; Khalil, Hps Abdul

    2013-01-01

    This study deals with the fabrication of composite matrix from saw dust (SD) and recycled polyethylene terephthalate (PET) at different ratio (w/w) by flat-pressed method. The wood plastic composites (WPCs) were made with a thickness of 6 mm after mixing the saw dust and PET in a rotary type blender followed by flat press process. Physical i.e., density, moisture content (MC), water absorption (WA) and thickness swelling (TS), and mechanical properties i.e., Modulus of Elasticity (MOE) and Modulus of Rupture (MOR) were assessed as a function of mixing ratios according to the ASTM D-1037 standard. WA and TS were measured after 24 hours of immersion in water at 25, 50 and 75°C temperature. It was found that density decreased 18.3% when SD content increased from 40% to 70% into the matix. WA and TS increased when the PET content decreased in the matrix and the testing water temperature increased. MOE and MOR were reached to maximum for the fabricated composites (2008.34 and 27.08 N/mm(2), respectively) when the SD content were only 40%. The results indicated that the fabrication of WPCs from sawdust and PET would technically feasible; however, the use of additives like coupling agents could further enhance the properties of WPCs. PMID:24324927

  12. Nd:YVO4 laser ablation of graphene films on glass and poly(ethylene terephthalate) substrates

    NASA Astrophysics Data System (ADS)

    Lee, Jeong Min; Lee, Jung-Hun; Han, Jae-Hee; Yoo, Ji-Beom; Lee, Jong-Ho; Cho, Seongjae; Kwon, Sang Jik; Cho, Eou Sik

    2014-08-01

    In this work, a novel processing technique for patterning of graphene monolayer prepared on various platforms, glass and poly(ethylene terephthalate) (PET) substrates, is suggested and experimented for its validity evaluation. Two process parameters of the Q-switched 1064 µm Nd:YVO4 laser system, scanning speed and repetition rate, were controlled for investigating the geometric features of the graphene line patterns and obtaining an optimum process conditions in the given laser system. The differences among line patterns acquired by controlled process conditions and substrate materials have been investigated and the underlying physics is contemplated. Multiple tools were utilized for evaluating the results, which included an optical microscopy for dimension check, Raman analysis, and G- and 2D-peak mapping technique. Continuous graphene line patterns have been successfully obtained from the most of the schemed process conditions and it would be revealed that the laser pattering is a plausible technique for patterning the graphene monolayers in fabricating various electronic and optical devices.

  13. A study of the glass transition in the amorphous interlamellar phase of highly crystallized poly(ethylene terephthalate)

    NASA Astrophysics Data System (ADS)

    Sellarès, J.; Diego, J. A.; Belana, J.

    2010-09-01

    The glass transition of poly(ethylene terephthalate) (PET) crystallized for 4 h at temperatures between 413 and 453 K was studied. Secondary crystallization processes were monitored by differential scanning calorimetry and the glass transition of the remaining interlamellar amorphous phase was studied by thermally stimulated depolarization currents measurements. Non-isothermal window polarization is employed to resolve the relaxation in modes with a well-defined relaxation time that is subsequently adjusted to several standard models. An analysis of experimental results reveals that cooperativity can be disregarded in the modelization of data. The evolution of modes during secondary crystallization, once primary crystallization has been completed, gives more weight to lower energy modes. As a consequence, secondary crystallization tends to lower the glass transition temperature of the amorphous interlamellar phase, although remaining noticeably higher than in amorphous samples. The evolution of calorimetric scans of the glass transition is simulated from the obtained results and shows the same behaviour. Regarding the glass transition temperature of the material, it can be concluded that primary and secondary crystallization act in opposite directions even though the effect of secondary crystallization is much smaller. The interpretation of these results in terms of current views about secondary crystallization is discussed.

  14. Covalent immobilization of lysozyme onto woven and knitted crimped polyethylene terephthalate grafts to minimize the adhesion of broad spectrum pathogens.

    PubMed

    Al Meslmani, Bassam M; Mahmoud, Gihan F; Leichtweiß, Thomas; Strehlow, Boris; Sommer, Frank O; Lohoff, Michael D; Bakowsky, Udo

    2016-01-01

    Graft-associated infections entirely determine the short-term patency of polyethylene terephthalate PET cardiovascular graft. We attempted to enzymatically inhibit the initial bacterial adhesion to PET grafts using lysozyme. Lysozyme was covalently immobilized onto woven and knitted forms of crimped PET grafts by the end-point method. Our figures of merit revealed lysozyme immobilization yield of 15.7 μg/cm(2), as determined by the Bradford assay. The activity of immobilized lysozyme on woven and knitted PET manifested 58.4% and 55.87% using Micrococcus lysodeikticus cells, respectively. Noteworthy, the adhesion of vein catheter-isolated Staphylococcus epidermidis decreased by 6- to 8-folds and of Staphylococcus aureus by 11- to 12-folds, while the Gram-negative Escherichia coli showed only a decrease by 3- to 4-folds. The anti-adhesion efficiency was specific for bacterial cells and no significant effect was observed on adhesion and growth of L929 cells. In conclusion, immobilization of lysozyme onto PET grafts can inhibit the graft-associated infection. PMID:26478289

  15. Preparation and in vitro evaluation of a biomimetic nanoscale calcium phosphate coating on a polyethylene terephthalate artificial ligament

    PubMed Central

    CHEN, CHEN; LI, HONG; GUO, CHANGAN; CHEN, SHIYI

    2016-01-01

    In the present study, a polyethylene terephthalate (PET) artificial ligament was coated with an organic layer-by-layer (LBL) self-assembled template of chitosan and hyaluronic acid, and then incubated in a calcium phosphate (CaP) solution to prepare a biomimetic CaP coating. The surface characterization of the ligament was examined using scanning electron microscopy, atomic force microscopy and energy-dispersive X-ray spectroscopy. The effects of CaP coatings on the osteogenic activity of MC3T3 E1 mouse osteoblastic cells were investigated by evaluating their attachment, proliferation and the relative expression levels of alkaline phosphatase. The results revealed that the organic LBL template on the PET artificial ligament was effective for CaP apatite formation. Following incubation for 72 h, numerous nanoscale CaP apatites were deposited on the PET ligament fibers. In addition, the results of the in vitro culture of MC3T3-E1 mouse osteoblastic cells demonstrated that the CaP coating had a good biocompatibility for cell proliferation and adhesion, and the CaP-coated group had a significantly higher alkaline phosphatase activity compared with the uncoated control group after seven days of cell culture. Collectively, these results demonstrated that the biomimetic nanoscale CaP-coated PET artificial ligaments have potential in bone-tissue engineering. PMID:27347053

  16. Evaluating organic compound migration in poly(ethylene terephthalate): a simple test with implications for polymer recycling.

    PubMed

    Sadler, G; Pierce, D; Lawson, A; Suvannunt, D; Senthil, V

    1996-01-01

    The safety of recycled plastics for food contact use is largely dictated by the ability of post-consumer organic contaminants to absorb into recycled materials and later diffuse from containers made from recycled plastics into the food supply. Diffusion and solubility data for organic contaminants in poly(ethylene terephthalate) (PET) are scarce. An approach for determining permeability constants, diffusion coefficients and solubility constants of slowly migrating contaminants in PET is described. Compounds (neat or in admixture) were heat-sealed in packets made from thin (0.00127 cm) PET films. Packets were placed in containers with GC sampling closures. Headspace (volatile compounds) or an external liquid medium (non-volatile compounds) was analysed for emergence of the compound. Diffusion coefficients were determined from non-steady state diffusion equations, permeability constants were determined from steady state permeation, and solubility constants were calculated from diffusion and permeability values. Diffusion coefficients (25 degrees C) ranged from 10(-9) to < 10(-16) cm2/s. The diffusion coefficient of benzene increased dramatically with concentration. Compounds with high permeation increased the transport rate of slower permeating volatiles. PMID:8950117

  17. Organometallic exposure dependence on organic–inorganic hybrid material formation in polyethylene terephthalate and polyamide 6 polymer fibers

    SciTech Connect

    Akyildiz, Halil I.; Jur, Jesse S.

    2015-03-15

    The effect of exposure conditions and surface area on hybrid material formation during sequential vapor infiltrations of trimethylaluminum (TMA) into polyamide 6 (PA6) and polyethylene terephthalate (PET) fibers is investigated. Mass gain of the fabric samples after infiltration was examined to elucidate the reaction extent with increasing number of sequential TMA single exposures, defined as the times for a TMA dose and a hold period. An interdependent relationship between dosing time and holding time on the hybrid material formation is observed for TMA exposure PET, exhibited as a linear trend between the mass gain and total exposure (dose time × hold time × number of sequential exposures). Deviation from this linear relationship is only observed under very long dose or hold times. In comparison, amount of hybrid material formed during sequential exposures to PA6 fibers is found to be highly dependent on amount of TMA dosed. Increasing the surface area of the fiber by altering its cross-sectional dimension is shown to have little on the reaction behavior but does allow for improved diffusion of the TMA into the fiber. This work allows for the projection of exposure parameters necessary for future high-throughput hybrid modifications to polymer materials.

  18. Comparative life cycle assessment and life cycle costing of four disposal scenarios for used polyethylene terephthalate bottles in Mauritius.

    PubMed

    Foolmaun, Rajendra Kumar; Ramjeeawon, Toolseeram

    2012-09-01

    The annual rise in population growth coupled with the flourishing tourism industry in Mauritius has lead to a considerable increase in the amount of solid waste generated. In parallel, the disposal of non-biodegradable wastes, especially plastic packaging and plastic bottles, has also shown a steady rise. Improper disposal of used polyethylene terephthalate (PET) bottles constitutes an eyesore to the environmental landscape and is a threat to the flourishing tourism industry. It is of utmost importance, therefore, to determine a suitable disposal method for used PET bottles which is not only environmentally efficient but is also cost effective. This study investigated the environmental impacts and the cost effectiveness of four selected disposal alternatives for used PET bottles in Mauritius. The four disposal routes investigated were: 100% landfilling; 75% incineration with energy recovery and 25% landfilling; 40% flake production (partial recycling) and 60% landfilling; and 75% flake production and 25% landfilling. Environmental impacts of the disposal alternatives were determined using ISO standardized life cycle assessment (LCA) and with the support of SimaPro 7.1 software. Cost effectiveness was determined using life cycle costing (LCC). Collected data were entered into a constructed Excel-based model to calculate the different cost categories, Net present values, damage costs and payback periods. LCA and LCC results indicated that 75% flake production and 25% landfilling was the most environmentally efficient and cost-effective disposal route for used PET bottles in Mauritius. PMID:23240194

  19. Formation of amorphous carbon on the surface of poly(ethylene terephthalate) by helium plasma based ion implantation

    NASA Astrophysics Data System (ADS)

    Tóth, A.; Veres, M.; Kereszturi, K.; Mohai, M.; Bertóti, I.; Szépvölgyi, J.

    2011-08-01

    The surface modification of poly(ethylene terephthalate) (PET) by helium plasma based ion implantation (He PBII) was studied. The effect of the main process parameters (acceleration voltage, fluence and fluence rate) on the alterations of the surface chemical composition and structure were investigated by X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. According to SRIM calculations, at ion energies above 2 keV the stopping power of PET for He + ions is dominated by the electronic component and the contribution of the nuclear component is relatively small. Degradation of the ester group and carbonisation were observed by XPS due to elimination of O-rich fragments. The total C-content of the modified layer increased with the increase of fluence rate and acceleration voltage of particles, enabling the purposeful alteration of the surface composition. A strong broadening was detected in the Raman spectrum between 1000 and 1700 cm -1, testifying to the intense formation of amorphous carbon. The area ratio of the D (˜1410 cm -1) to G (˜1570 cm -1) band increased with the increase of particle fluence and the increase of acceleration voltage, offering the possibility of tailoring the chemical structure of the amorphous carbon layer created by the He PBII treatment.

  20. Stepwise crystallization and the layered distribution in crystallization kinetics of ultra-thin poly(ethylene terephthalate) film

    NASA Astrophysics Data System (ADS)

    Zuo, Biao; Xu, Jianquan; Sun, Shuzheng; Liu, Yue; Yang, Juping; Zhang, Li; Wang, Xinping

    2016-06-01

    Crystallization is an important property of polymeric materials. In conventional viewpoint, the transformation of disordered chains into crystals is usually a spatially homogeneous process (i.e., it occurs simultaneously throughout the sample), that is, the crystallization rate at each local position within the sample is almost the same. Here, we show that crystallization of ultra-thin poly(ethylene terephthalate) (PET) films can occur in the heterogeneous way, exhibiting a stepwise crystallization process. We found that the layered distribution of glass transition dynamics of thin film modifies the corresponding crystallization behavior, giving rise to the layered distribution of the crystallization kinetics of PET films, with an 11-nm-thick surface layer having faster crystallization rate and the underlying layer showing bulk-like behavior. The layered distribution in crystallization kinetics results in a particular stepwise crystallization behavior during heating the sample, with the two cold-crystallization temperatures separated by up to 20 K. Meanwhile, interfacial interaction is crucial for the occurrence of the heterogeneous crystallization, as the thin film crystallizes simultaneously if the interfacial interaction is relatively strong. We anticipate that this mechanism of stepwise crystallization of thin polymeric films will allow new insight into the chain organization in confined environments and permit independent manipulation of localized properties of nanomaterials.

  1. Nd:YVO4 laser direct ablation of indium tin oxide films deposited on glass and polyethylene terephthalate substrates.

    PubMed

    Wang, Jian-Xun; Kwon, Sang Jik; Han, Jae-Hee; Cho, Eou Sik

    2013-09-01

    A Q-switched diode-pumped neodymium-doped yttrium vanadate (Nd:YVO4, lambda = 1064 nm) laser was applied to obtain the indium tin oxide (ITO) patterns on flexible polyethylene terephthalate (PET) substrate by a direct etching method. After the ITO films were deposited on a soda-lime glass and PET substrate, laser ablations were carried out on the ITO films for various conditions and the laser ablated results on the ITO films were investigated and analyzed considering the effects of substrates on the laser etching. The laser ablated widths on ITO deposited on glass were found to be much narrower than those on ITO deposited on PET substrate, especially, at a higher scanning speed of laser beam such as 1000 mm/s and 2000 mm/s. As the thermal conductivity of glass substrate is about 7.5 times higher than that of PET, more thermal energy would be spread and transferred to lateral direction in the ITO film in case of PET substrate. PMID:24205645

  2. Antimicrobial nano-silver non-woven polyethylene terephthalate fabric via an atmospheric pressure plasma deposition process

    PubMed Central

    Deng, Xiaolong; Yu Nikiforov, Anton; Coenye, Tom; Cools, Pieter; Aziz, Gaelle; Morent, Rino; De Geyter, Nathalie; Leys, Christophe

    2015-01-01

    An antimicrobial nano-silver non-woven polyethylene terephthalate (PET) fabric has been prepared in a three step process. The fabrics were first pretreated by depositing a layer of organosilicon thin film using an atmospheric pressure plasma system, then silver nano-particles (AgNPs) were incorporated into the fabrics by a dipping-dry process, and finally the nano-particles were covered by a second organosilicon layer of 10-50 nm, which acts as a barrier layer. Different surface characterization techniques like SEM and XPS have been implemented to study the morphology and the chemical composition of the nano-silver fabrics. Based on these techniques, a uniform immobilization of AgNPs in the PET matrix has been observed. The antimicrobial activity of the treated fabrics has also been tested using P. aeruginosa, S. aureus and C. albicans. It reveals that the thickness of the barrier layer has a strong effect on the bacterial reduction of the fabrics. The durability and stability of the AgNPs on the fabrics has also been investigated in a washing process. By doing so, it is confirmed that the barrier layer can effectively prevent the release of AgNPs and that the thickness of the barrier layer is an important parameter to control the silver ions release. PMID:25951432

  3. Antimicrobial nano-silver non-woven polyethylene terephthalate fabric via an atmospheric pressure plasma deposition process

    NASA Astrophysics Data System (ADS)

    Deng, Xiaolong; Yu Nikiforov, Anton; Coenye, Tom; Cools, Pieter; Aziz, Gaelle; Morent, Rino; de Geyter, Nathalie; Leys, Christophe

    2015-05-01

    An antimicrobial nano-silver non-woven polyethylene terephthalate (PET) fabric has been prepared in a three step process. The fabrics were first pretreated by depositing a layer of organosilicon thin film using an atmospheric pressure plasma system, then silver nano-particles (AgNPs) were incorporated into the fabrics by a dipping-dry process, and finally the nano-particles were covered by a second organosilicon layer of 10-50 nm, which acts as a barrier layer. Different surface characterization techniques like SEM and XPS have been implemented to study the morphology and the chemical composition of the nano-silver fabrics. Based on these techniques, a uniform immobilization of AgNPs in the PET matrix has been observed. The antimicrobial activity of the treated fabrics has also been tested using P. aeruginosa, S. aureus and C. albicans. It reveals that the thickness of the barrier layer has a strong effect on the bacterial reduction of the fabrics. The durability and stability of the AgNPs on the fabrics has also been investigated in a washing process. By doing so, it is confirmed that the barrier layer can effectively prevent the release of AgNPs and that the thickness of the barrier layer is an important parameter to control the silver ions release.

  4. Antimicrobial nano-silver non-woven polyethylene terephthalate fabric via an atmospheric pressure plasma deposition process.

    PubMed

    Deng, Xiaolong; Nikiforov, Anton Yu; Coenye, Tom; Cools, Pieter; Aziz, Gaelle; Morent, Rino; De Geyter, Nathalie; Leys, Christophe

    2015-01-01

    An antimicrobial nano-silver non-woven polyethylene terephthalate (PET) fabric has been prepared in a three step process. The fabrics were first pretreated by depositing a layer of organosilicon thin film using an atmospheric pressure plasma system, then silver nano-particles (AgNPs) were incorporated into the fabrics by a dipping-dry process, and finally the nano-particles were covered by a second organosilicon layer of 10-50 nm, which acts as a barrier layer. Different surface characterization techniques like SEM and XPS have been implemented to study the morphology and the chemical composition of the nano-silver fabrics. Based on these techniques, a uniform immobilization of AgNPs in the PET matrix has been observed. The antimicrobial activity of the treated fabrics has also been tested using P. aeruginosa, S. aureus and C. albicans. It reveals that the thickness of the barrier layer has a strong effect on the bacterial reduction of the fabrics. The durability and stability of the AgNPs on the fabrics has also been investigated in a washing process. By doing so, it is confirmed that the barrier layer can effectively prevent the release of AgNPs and that the thickness of the barrier layer is an important parameter to control the silver ions release. PMID:25951432

  5. Utilization of waste polyethylene terephthalate as a reducing agent in the reduction of iron ore composite pellets

    NASA Astrophysics Data System (ADS)

    Polat, Gökhan; Birol, Burak; Sarıdede, Muhlis Nezihi

    2014-08-01

    The increasing consumption of plastics inevitably results in increasing amounts of waste plastics. Because of their long degradation periods, these wastes negatively affect the natural environment. Numerous studies have been conducted to recycle and eliminate waste plastics. The potential for recycling waste plastics in the iron and steel industry has been underestimated; the high C and H contents of plastics may make them suitable as alternative reductants in the reduction process of iron ore. This study aims to substitute plastic wastes for coal in reduction melting process and to investigate their performance during reduction at high temperature. We used a common type of waste plastic, polyethylene terephthalate (PET), because of its high carbon and hydrogen contents. Composite pellets containing PET wastes, coke, and magnetite iron ore were reduced at selected temperatures of 1400 and 1450°C for reduction time from 2 to 10 min to investigate the reduction melting behavior of these pellets. The results showed that an increased temperature and reduction time increased the reduction ratio of the pellets. The optimum experimental conditions for obtaining metallic iron (iron nuggets) were reduction at 1450°C for 10 min using composite pellets containing 60% PET and 40% coke.

  6. Chemical modification of poly(ethylene terephthalate) and immobilization of the selected enzymes on the modified film

    NASA Astrophysics Data System (ADS)

    Irena, Gancarz; Jolanta, Bryjak; Karolina, Zynek

    2009-07-01

    Poly(ethylene terephthalate) (PET) film was modified by reaction with hydrazine (HD), ethylenediamine (EDA), 1,2-diaminopropane (1,2-DAP) and 1,3-diaminopropane (1,3-DAP). The maximal amount of amine functionalities introduced in the chosen conditions on the surface was found as 0.07, 3.35, 0.76 and 1.99 nmol cm -2 for HD, EDA, 1,2-DAP and 1,3-DAP respectively. During the modification process etching of the sample and an increase of stiffness takes place. FTIR-ATR spectra prove that the surface chemistry after modification in amine solution is very complex. The lack of clear correlation between the surface tension and surface concentration of amine functionalities seems to confirm that. For immobilization purpose invertase, laccase and tyrosinase were used. The amount of covalently attached proteins at first increases with the increase of surface concentration of amine groups but after reaching a certain level of amine groups, decrease of the immobilization level was observed. All enzymes tested showed highest activity for a moderate level of aminolysis and this activity had the highest values for EDA-modified PET.

  7. Adsorption of surfactin produced from Bacillus subtilis using nonwoven PET (polyethylene terephthalate) fibrous membranes functionalized with chitosan.

    PubMed

    Behary, N; Perwuelz, A; Campagne, C; Lecouturier, D; Dhulster, P; Mamede, A S

    2012-02-01

    This article deals with an alternative method for bio-separation of surfactin produced by Bacillus subtilis using sorption method on nonwoven PET (polyethylene terephthalate) fibrous membranes functionalized with chitosan. In the first part of the study, surface functionalization of the PET nonwoven fibrous membranes is carried out with aqueous 65% deacetylated chitosan solution with or without a prior surface activation using air-atmospheric plasma treatment. Very small modification of the PET fibrous nonwoven air-permeability confirms the functionalization of PET fibre surface with little reduction of membrane porosity. The functionalized membranes are then characterized by physico-chemical methods: X-ray Photoelectron Spectroscopy (XPS), Wettability and zeta potential. Chitosan increases drastically the zeta potential of PET at all pH values though a prior plasma treatment of the PET membrane reduces slightly the increase in zeta potential values. Sorption of surfactin quantified by HPLC shows that the extent of surfactin sorption on PET nonwovens depends on the surface functionalization method. Surface functionalization with chitosan results in immediate sorption of the entire quantity of surfactin. A prior surface activation by air atmospheric plasma treatment of the PET membranes before chitosan application retards the sorption of entire surfactin which takes place after 1.5h, only. Increased zeta potential and increased hydrophobic behavior in the presence of chitosan without plasma activation would explain the interesting surfactin sorption results. PMID:22056081

  8. Solvent-free vapor-phase photografting of acrylamide onto poly(ethylene terephthalate).

    PubMed

    Wirsén, Anders; Sun, Hui; Albertsson, Ann-Christine

    2005-01-01

    Poly(ethylene terphthalate) (PET) films were photografted under reduced pressure in a solvent-free vapor of acrylamide and a co-initiator, benzophenone. Characterization of grafted samples by ESCA and contact angles showed that the grafting increased with grafting time and temperature. The amide groups obtained by the acrylamide grafting were converted into amine groups by the Hofmann rearrangement to be used in coupling reactions. The amine groups were confirmed by reaction with pentafluorobenzoyl chloride, which provides a fluorine label for ESCA. Surface grafting of polymeric substrates in the vapor phase induced by plasma or high energy and UV irradiation is reviewed. PMID:16153108

  9. Deep micro-machining of poly-ethylene terephthalate for plastic MEMS applications

    NASA Astrophysics Data System (ADS)

    Pajouhi, H.; Mohajerzadeh, S.; Nayeri, F.; Sanaee, Z.

    2010-12-01

    Etching of poly-ethylene terephathalate (PET) is achieved using a chemical solution in di-methyl-formamide assisted by ultra-violet illumination. Deep vertical features suitable for plastic micro-machining, are obtained with features of the order of 2 μm and aspect ratios of the order of 10. By using tin (Sn) as the masking layer, the problem of crack formation on the PET surface during this photochemical etching technique is totally resolved. High etch-rates as 20 μm/h are obtained at a low etching temperature of 60 °C. To improve the thermal dissipation during the etching and to minimize the plastic shrinkage, a layer of silicone-rubber is applied on the backside of the PET. We have successfully fabricated and assembled an all-plastic one directional micro-valve. Preliminary plastic-based micro-structures are demonstrated.

  10. On the Diels-Alder approach to solely biomass-derived polyethylene terephthalate (PET): conversion of 2,5-dimethylfuran and acrolein into p-xylene.

    PubMed

    Shiramizu, Mika; Toste, F Dean

    2011-10-24

    Polyethylene terephthalate (PET) is a polymeric material with high global demand. Conventionally, PET is produced from fossil-fuel-based materials. Herein, we explored the feasibility of a sustainable method for PET production by using solely bio-renewable resources. Specifically, 2,5-dimethylfuran (derived from lignocellulosic biomass through 5-(hydroxymethyl)furfural) and acrolein (produced from glycerol, a side product of biodiesel production) were converted into the key intermediate p-xylene (a precursor of terephthalic acid). This synthesis consists of a sequential Diels-Alder reaction, oxidation, dehydration, and decarboxylation. In particular, the pivotal first step, the Diels-Alder reaction, was studied in detail to provide useful kinetic and thermodynamic data. Although it was found that this reaction requires low temperature to proceed efficiently, which presents a limitation on economic feasibility on an industrial scale, the concept was realized and bio-derived p-xylene was obtained in 34% overall yield over four steps. PMID:21922576

  11. Combustion of bisphenol-A-polycarbonate, polyethylene terephthalate and cellulose in a laboratory scale thermal destruction facility

    SciTech Connect

    Missoum, A.; Gupta, A.K.; Keating, E.L.

    1995-12-31

    Results of combustion tests are presented from the laboratory scale thermal destruction facility on samples containing varying composition of bisphenol-A-polycarbonate (PC) and polyethylene terephthalate (PET) mixed with non-plastic material (cellulose). The equivalence ratio was varied from 0.5 to 2.0. Data provides the effect of temperature, equivalence ratio and the chemical composition of the surrogate solid waste on the emissions of NO{sub x}, CO, CO{sub 2}, HC and O{sub 2}. Thermal destruction behavior of the surrogate waste is qualitatively observed to be enhanced with progressive increase in temperature which results in maximum volume reduction and low NO{sub x} emissions for these combustion tests. The numerical calculations using equilibrium conditions show similar trends to those obtained experimentally. The measured CO emissions were lower than the calculated ones but the CO{sub 2} and HC emissions were higher than the calculated values. In all tests the measured O{sub 2} concentrations were higher than the calculated ones and the NO{sub x} concentrations were lower at higher equivalence ratios. Analysis and interpretation of the data reveal that the composition of the waste as well as the conditions under which the thermal destruction process takes place, i.e., temperature, equivalence ratio and process type have significant influence on the emissions. These results show significant effect of controlled combustion on the amount and nature of species formed. This information can assist in developing strategies in the design and operation of thermal destruction systems.

  12. Development of Iron-Chelating Poly(ethylene terephthalate) Packaging for Inhibiting Lipid Oxidation in Oil-in-Water Emulsions.

    PubMed

    Johnson, David R; Tian, Fang; Roman, Maxine J; Decker, Eric A; Goddard, Julie M

    2015-05-27

    Foods such as bulk oils, salad dressings, and nutritionally fortified beverages that are susceptible to oxidative degradation are often packaged in poly(ethylene terephthalate) (PET) bottles with metal chelators added to the food to maintain product quality. In the present work, a metal-chelating active packaging material is designed and characterized, in which poly(hydroxamic acid) (PHA) metal-chelating moieties were grafted from the surface of PET. Biomimetic PHA groups were grafted in a two-step UV-initiated process without the use of a photoinitiator. Surface characterization of the films by attenuated total reflective Fourier transform infrared spectroscopy (ATR-FTIR) and scanning electron microscopy (SEM) suggested successful grafting and conversion of poly(hydroxyethyl acrylate) (PHEA) to PHA chelating moieties from the surface of PET. Colorimetric (ferrozine) and inductively coupled plasma mass spectroscopy (ICP-MS) assays demonstrated the ability of PET-g-PHA to chelate iron in a low-pH (3.0) environment containing a competitive metal chelator (citric acid). Lipid oxidation studies demonstrated the antioxidant activity of PET-g-PHA films in inhibiting iron-promoted oxidation in an acidified oil-in-water (O/W) emulsion model system (pH 3.0). Particle size and ζ-potential analysis indicated that the addition of PET-g-PHA films did not affect the physical stability of the emulsion system. This work suggests that biomimetic chelating moieties can be grafted from PET and effectively inhibit iron-promoted degradation reactions, enabling removal of metal-chelating additives from product formulations. PMID:25985711

  13. Uterotrophic and Hershberger assays for endocrine disruption properties of plastic food contact materials polypropylene (PP) and polyethylene terephthalate (PET).

    PubMed

    Chung, Bu Young; Kyung, Minji; Lim, Seong Kwang; Choi, Seul Min; Lim, Duck Soo; Kwack, Seung Jun; Kim, Hyung Sik; Lee, Byung-Mu

    2013-01-01

    Plasticizers or plastic materials such as phthalates, bisphenol-A (BPA), and styrene are widely used in the plastic industry and are suspected endocrine-disrupting chemicals (EDC). Although plastic materials such as polypropylene (PP) and polyethylene terephthalate (PET) are not EDC and are considered to be safe, their potential properties as EDC have not been fully investigated. In this study, plastic samples eluted from plastic food containers (PP or PET) were investigated in Sprague-Dawley rats using Hershberger and uterotrophic assays. In the Hershberger assay, 6-wk-old castrated male rats were orally treated for 10 consecutive days with plastic effluent at 3 different doses (5 ml/kg) or vehicle control (corn oil, 1 ml/100 g) to determine the presence of both anti-androgenic and androgenic effects. Testosterone (0.4 mg/ml/kg) was subcutaneously administered for androgenic evaluation as a positive control, whereas testosterone (0.4 mg/ml/kg) and flutamide (3 mg/kg/day) were administered to a positive control group for anti-androgenic evaluation. The presence of any anti-androgenic or androgenic activities of plastic effluent was not detected. Sex accessory tissues such as ventral prostate or seminal vesicle showed no significant differences in weight between treated and control groups. For the uterotrophic assay, immature female rats were treated with plastic effluent at three different doses (5 ml/kg), with vehicle control (corn oil, 1 ml/100 g), or with ethinyl estradiol (3 μg/kg/d) for 3 d. There were no significant differences between test and control groups in vagina or uterine weight. Data suggest that effluents from plastic food containers do not appear to produce significant adverse effects according to Hershberger and uterotrophic assays. PMID:23862761

  14. Activated carbons from coal/pitch and polyethylene terephthalate blends for the removal of phenols from aqueous solutions

    SciTech Connect

    Ewa Lorenc-Grabowska; Grazyna Gryglewicz; Jacek Machnikowski

    2009-05-15

    Blends of two bituminous coals and a coal-tar pitch (CTP) with polyethylene terephthalate (PET) were evaluated as precursors of activated carbons (ACs). The intensity of the interactions between the raw materials, coal/CTP and PET during copyrolysis was closely observed by means of thermogravimetric analysis. In addition, the homogeneity of the carbon matrix of the chars produced at 800{sup o}C in a horizontal oven was studied by polarized light optical microscopy. Activated carbons were prepared from single components and their blends (1:1 w/w) by subjecting them to carbonization up to 800{sup o}C in a horizontal oven and then activation with steam at 800{sup o}C to 50% burnoff. The porous structure of the ACs was determined by sorption of N{sub 2} at 77 K and of CO{sub 2} at 273 K. The PET-containing blends produced microporous activated carbons with a maximum BET surface area of nearly 1100 m{sup 2} g{sup -1} and a maximum micropore size distribution of 0.6-0.8 nm in the case of the AC from the CTP/PET blend. The addition of PET to a bituminous coal was compared with the preoxidation of coal P in air as a way to reduce thermoplasticity and to promote the development of the porous structure. The modification of bituminous coals by PET appeared to be more effective than conventional coal preoxidation treatment. The resultant ACs were tested by measuring their effectiveness in removing phenols from an aqueous solution. The adsorption of p-chlorophenol (PCP) by the ACs prepared from the PET-containing blends was slightly higher than for the commercial activated carbon. The ability to adsorb PCP was found to be related to the volume of the super-micropores.

  15. Synergistic Effect of Atmospheric Pressure Plasma Pre-Treatment on Alkaline Etching of Polyethylene Terephthalate Fabrics and Films

    NASA Astrophysics Data System (ADS)

    A. Elabid Amel, E.; Guo, Ying; Shi, Jianjun; Ding, Ke; Zhang, Jing

    2016-04-01

    Dyeing of PET materials by traditional methods presents several problems. Plasma technology has received enormous attention as a solution for the environmental problems related with textile surface modifications, and there has been a rapid development and commercialization of plasma technology over the past decade. In this work, the synergistic effect of atmospheric pressure plasma on alkaline etching and deep coloring of dyeing properties on polyethylene terephthalate (PET) fabrics and films was investigated. The topographical changes of the PET surface were investigated by atomic force microscopy (AFM) images, which revealed a smooth surface morphology of the untreated sample whereas a high surface roughness for the plasma and/or alkaline treated samples. The effects of atmospheric pressure plasma on alkaline etching of the structure and properties of PET were investigated by means of differential scanning calorimetry (DSC), the main objective of performing DSC was to investigate the effect of the plasma pre-treatment on the Tg and Tm. Using a tensile strength tester YG065H and following a standard procedure the maximum force and elongation at maximum force of PET materials was investigated. Oxygen and argon plasma pre-treatment was found to increase the PET fabric weight loss rate. The color strength of PET fabrics was increased by various plasma pre-treatment times. The penetration of plasma and alkaline reactive species deep into the PET structure results in better dyeability and leaves a significant effect on the K/S values of the plasma pre-treated PET. It indicated that plasma pre-treatment has a great synergistic effect with the alkaline treatment of PET.

  16. Polyethylenimine modified poly(ethylene terephthalate) capillary channeled-polymer fibers for anion exchange chromatography of proteins.

    PubMed

    Jiang, Liuwei; Jin, Yi; Marcus, R Kenneth

    2015-09-01

    Native poly(ethylene terephthalate) (PET) capillary-channeled polymer (C-CP) fibers have been previously studied as stationary phases for reversed phase and affinity protein separations. In this study, surface modified PET C-CP fibers were evaluated for the anion exchange separation of proteins. The native PET C-CP fibers were aminated using polyethylenimine (PEI) followed by a 1,4-butanediol diglycidyl ether (BUDGE) cross-linking step. Subsequent PEI/BUDGE treatments can be employed to further develop the polyamine layer on the fiber surfaces. The PEI densities of the modified fibers were quantified through the ninhydrin reaction, yielding values of 0.43-0.89μmolg(-1). The surface modification impact on column permeability was found to be 0.66×10(-11) to 1.33×10(-11)m(2), depending on the modification time and conditions. The dynamic binding capacities of the modified fiber media were determined to be 1.99-8.54mgmL(-1) bed volume, at linear velocities of 88-438cmmin(-1) using bovine serum albumin as the model protein. It was found that increasing the mobile phase linear velocity (up to 438cmmin(-1)) had no effect on the separation quality for a synthetic protein mixture, reflecting the lack of van Deemter C-term effects for the C-CP fiber phase. The low-cost, easy modification method and the capability of fast protein separation illustrate great potential in the use of PEI/BUDGE-modified PET C-CP fibers for high-throughput protein separation and downstream processing. PMID:26253835

  17. Improving the low temperature dyeability of polyethylene terephthalate fabric with dispersive dyes by atmospheric pressure plasma discharge

    NASA Astrophysics Data System (ADS)

    Elabid, Amel E. A.; Zhang, Jie; Shi, Jianjun; Guo, Ying; Ding, Ke; Zhang, Jing

    2016-07-01

    Polyethylene terephthalate (PET) fiber and textile is one of the largest synthetic polymer commodity in the world. The great energy consumption and pollution caused by the high temperature and pressure dyeing of PET fibers and fabrics with disperse dyes has been caused concern these years. In this study, an atmospheric pressure plasma with fine and uniform filament discharge operated at 20 kHz has been used to improve the low temperature dyeability of PET fabric at 95 °C with three cation disperse dyes: Red 73, Blue 183 and Yellow 211. The dyes uptake percentage of the treated PET fabrics was observed to increase as twice as much of untreated fabric. The color strength rate was increased more than 20%. The reducing of the water contact angle and the raising of the capillary height of treated PET fabric strip indicate its hydrophilicity improvement. Scanning electron microscope (SEM) results display nano to micro size of etching pits appeared uniformly on the fiber surface of the treated PET. Simultaneously, X-ray photoelectron spectroscopy (XPS) analysis indicates an increase of the oxygen content in the surface caused by the introduction of polar groups such as Cdbnd O and COOH. The rough surface with improved polar oxygen groups showed hydrophilicity and affinity to C.I. dispersive dyes and is believed to be caused by the strong and very fine filament discharge appearing randomly at one place at an instant but evenly at many places at a longer period. This increases the diffusion and absorption of the C.I. disperse dyes on the PET fiber surface, which improve its low temperature dyeability.

  18. High density polyethylene (HDPE)/poly(ethylene terephthalate) (PET) polymer blend studies related to recycling co-mingled plastics

    NASA Astrophysics Data System (ADS)

    Tsai, Pang-Yen

    Polymer blends of virgin high density polyethylene (HDPE) and poly(ethylene terephthalate) (PET) were studied as an attempt to relate the microstructure to the mechanical properties of the blends. The virgin blends were prepared by extrusion and then injection molded into specimens for characterization. Two of the virgin blends were tested for possible compatibilization using a styrene-ethylene-butylene-styrene (SEBS) block copolymer. In addition, six blends of post-consumer resins (PCRs) of HDPE and PET were included in this work for comparison. The moduli of the virgin blends showed positive deviation from those expected from the rule of mixtures. The synergism of the composite moduli can be explained partly by a Poisson's effect. Yield strengths of the blends molded at low injection chamber temperatures (200sp°, 230sp°, and 250sp°C) followed the rule of mixtures well, because PET filaments found in the composites had very high length to diameter ratios. When the injection chamber temperature was above the PET melting point (˜254sp°C), PET filaments were found to break down into particles, and the yield strengths of the blends coincided with the values expected from the inverse rule of mixtures. Impact strengths of the virgin blends were much less than that of a HDPE homopolymer due to poor interfacial bonding between HDPE and PET. Compatibilization appeared to be advantageous since it dramatically improved the impact strength of the virgin blends. SEM micrographs of impact fractured surfaces revealed that the improved adhesion from compatibilization and the presence of numerous uniaxially aligned PET filaments in the HDPE substrate can account for the significant increases in fracture resistance of the compatibilized blends. Mechanical performance of the PCRs was inferior to that of the virgin blends. Aside from polymer degradation and contamination due to repeated processing and handling, absence of PET filaments and interfacial bonding could be

  19. Waste polyethylene terephthalate (PET) materials as sustainable precursors for the synthesis of nanoporous MOFs, MIL-47, MIL-53(Cr, Al, Ga) and MIL-101(Cr).

    PubMed

    Lo, Sheng-Han; Senthil Raja, Duraisamy; Chen, Chia-Wei; Kang, Yu-Hao; Chen, Jiun-Jen; Lin, Chia-Her

    2016-06-21

    In our novel green approach, the waste polyethylene terephthalate (PET) bottle material has effectively been used as the starting precursor instead of terephthalic acid for the synthesis of five terephthalate based nanoporous trivalent metal-organic frameworks (MOFs) namely MIL-47, MIL-53(Cr), MIL-53(Al), MIL-53(Ga), and MIL-101(Cr). The optimum reaction parameters to achieve the green synthesis were studied. These MOFs were structurally identified by using powder X-ray diffraction (PXRD) measurements. Scanning electron microscopy (SEM) images confirm the particle nature and size of the synthesized MOFs. Nitrogen gas sorption measurements have been done for some of the MOFs to check their porous properties. All the characterization techniques strongly supported that the synthesized MOFs using PET are similar to their literature reports. The gas adsorption studies for the synthesized MIL-53(Cr) and MIL-101(Cr) showed their significant gas uptake capability towards CO2 and H2 gases. Further, the synthesized MIL-47 and MIL-101(Cr) have been tested for their catalytic ability in chemical fixation of CO2 gas through the conversion of CO2 and epoxides to the corresponding cyclic carbonates which shows promising results to use them as catalysts. PMID:27198203

  20. An evaluation of the migration of antimony from polyethylene terephthalate (PET) plastic used for bottled drinking water.

    PubMed

    Chapa-Martínez, C A; Hinojosa-Reyes, L; Hernández-Ramírez, A; Ruiz-Ruiz, E; Maya-Treviño, L; Guzmán-Mar, J L

    2016-09-15

    The leaching of antimony (Sb) from polyethylene terephthalate (PET) bottling material was assessed in twelve brands of bottled water purchased in Mexican supermarkets by atomic fluorescence spectrometry with a hydride generation system (HG-AFS). Dowex® 1X8-100 ion-exchange resin was used to preconcentrate trace amounts of Sb in water samples. Migration experiments from the PET bottle material were performed in water according to the following storage conditions: 1) temperature (25 and 75°C), 2) pH (3 and 7) and 3) exposure time (5 and 15days), using ultrapure water as a simulant for liquid foods. The test conditions were studied by a 2(3) factorial experimental design. The Sb concentration measured in the PET packaging materials varied between 73.0 and 111.3mg/kg. The Sb concentration (0.28-2.30μg/L) in all of the PET bottled drinking water samples examined at the initial stage of the study was below the maximum contaminant level of 5μg/L prescribed by European Union (EU) regulations. The parameters studied (pH, temperature, and storage time) significantly affected the release of Sb, with temperature having the highest positive significant effect within the studied experimental domain. The highest Sb concentration leached from PET containers was in water samples at pH7 stored at 75°C for a period of 5days. The extent of Sb leaching from the PET ingredients for different brands of drinking water can differ by as much as one order of magnitude in experiments conducted under the worst-case conditions. The chronic daily intake (CDI) caused by the release of Sb in one brand exceeded the Environmental Protection Agency (USEPA) regulated CDI value of 400ng/kg/day, with values of 514.3 and 566.2ng/kg/day for adults and children. Thus, the appropriate selection of the polymer used for the production of PET bottles seems to ensure low Sb levels in water samples. PMID:27192700

  1. Impact of temperature and storage duration on the chemical and odor quality of military packaged water in polyethylene terephthalate bottles.

    PubMed

    Greifenstein, Michael; White, Duvel W; Stubner, Alex; Hout, Joseph; Whelton, Andrew J

    2013-07-01

    The impact of temperature and storage time on military packaged water (MPW) quality was examined at four temperatures (23.0 °C to 60.0 °C) for 120 days. Polyethylene terephthalate (PET) bottles were filled in California and Afghanistan with unbuffered water treated by reverse osmosis. The US military's water pH long-term potability standard was exceeded, and US Food and Drug Administration (USFDA) and US Environmental Protection Agency (USEPA) drinking water pH and odor intensity limits were also exceeded. During a 70 day exposure period, Port Hueneme MPW total organic carbon and total trihalomethane levels increased from < 0.25mg/L to 2.0 ± 0.0mg/L and <0.05 μg/L to 51.5 ± 2.1 μg/L, respectively. PET released organic contaminants into MPW and residual disinfectant generated trihalomethane contaminants. After 14 days at 37.7 °C and 60.0 °C, Afghanistan MPW threshold odor number values were 8.0 and 8.6, respectively. Total organic carbon concentration only increased with exposure duration at 60.0 °C. Acetaldehyde and formaldehyde contaminants were not detected likely due to the high method detection limits applied in this study. Phthalate contaminants detected and their maximum levels were butylbenzylphthalate (BBP) 0.43 μg/L, di-n-butylphthalate (DnBP) 0.38 μg/L, di(2-ethylhexyl)phthalate (DEHP) 0.6 μg/L, and diethylphthalate (DEP) 0.32 μg/L. Antimony was only detected in 60.0 °C Afghanistan MPW on Day 28 and beyond, and its maximum concentration was 3.6 ± 0.3 μg/L. No antimony was found in bottles exposed to lesser temperatures. Environmental health, PET synthesis and bottle manufacturers, and bottle users can integrate results of this work to improve health protective decisions and doctrine. PMID:23624011

  2. Safety evaluation of mechanical recycling processes used to produce polyethylene terephthalate (PET) intended for food contact applications.

    PubMed

    Barthélémy, E; Spyropoulos, D; Milana, M-R; Pfaff, K; Gontard, N; Lampi, E; Castle, L

    2014-01-01

    The development of a scheme for the safety evaluation of mechanical recycling processes for polyethylene terephthalate (PET) is described. The starting point is the adoption of a threshold of toxicological concern such that migration from the recycled PET should not give rise to a dietary exposure exceeding 0.0025 μg kg(-1) bw day(-1), the exposure threshold value for chemicals with structural alerts raising concern for potential genotoxicity, below which the risk to human health would be negligible. It is practically impossible to test every batch of incoming recovered PET and every production batch of recycled PET for all the different chemical contaminants that could theoretically arise. Consequently, the principle of the safety evaluation is to measure the cleaning efficiency of a recycling process by using a challenge test with surrogate contaminants. This cleaning efficiency is then applied to reduce a reference contamination level for post-consumer PET, conservatively set at 3 mg kg(-1) PET for a contaminant resulting from possible misuse by consumers. The resulting residual concentration of each contaminant in recycled PET is used in conservative migration models to calculate migration levels, which are then used along with food consumption data to give estimates of potential dietary exposure. The default scenario, when the recycled PET is intended for general use, is that of an infant weighing 5 kg and consuming every day powdered infant formula reconstituted with 0.75 L of water coming from water bottles manufactured with 100% recycled PET. According to this scenario, it can be derived that the highest concentration of a substance in water that would ensure that the dietary exposure of 0.0025 µg kg(-1) bw day(-1) is not exceeded, is 0.017 μg kg(-1) food. The maximum residual content that would comply with this migration limit depends on molecular weight and is in the range 0.09-0.32 mg kg(-1) PET for the typical surrogate contaminants

  3. Static liquid permeation cell method for determining the migration parameters of low molecular weight organic compounds in polyethylene terephthalate.

    PubMed

    Song, Yoon S; Koontz, John L; Juskelis, Rima O; Zhao, Yang

    2013-01-01

    The migration of low molecular weight organic compounds through polyethylene terephthalate (PET) films was determined by using a custom permeation cell assembly. Fatty food simulant (Miglyol 812) was added to the receptor chamber, while the donor chamber was filled with 1% and 10% (v/v) migrant compounds spiked in simulant. The permeation cell was maintained at 40°C, 66°C, 100°C or 121°C for up to 25 days of polymer film exposure time. Migrants in Miglyol were directly quantified without a liquid-liquid extraction step by headspace-GC-MS analysis. Experimental diffusion coefficients (DP) of toluene, benzyl alcohol, ethyl butyrate and methyl salicylate through PET film were determined. Results from Limm's diffusion model showed that the predicted DP values for PET were all greater than the experimental values. DP values predicted by Piringer's diffusion model were also greater than those determined experimentally at 66°C, 100°C and 121°C. However, Piringer's model led to the underestimation of benzyl alcohol (Áp = 3.7) and methyl salicylate (Áp = 4.0) diffusion at 40°C with its revised "upper-bound" Áp value of 3.1 at temperatures below the glass transition temperature (Tg) of PET (<70°C). This implies that input parameters of Piringer's model may need to be revised to ensure a margin of safety for consumers. On the other hand, at temperatures greater than the Tg, both models appear too conservative and unrealistic. The highest estimated Áp value from Piringer's model was 2.6 for methyl salicylate, which was much lower than the "upper-bound" Áp value of 6.4 for PET. Therefore, it may be necessary further to refine "upper-bound" Áp values for PET such that Piringer's model does not significantly underestimate or overestimate the migration of organic compounds dependent upon the temperature condition of the food contact material. PMID:23883310

  4. One-step sonochemical synthesis of a graphene oxide-manganese oxide nanocomposite for catalytic glycolysis of poly(ethylene terephthalate)

    NASA Astrophysics Data System (ADS)

    Park, Gle; Bartolome, Leian; Lee, Kyoung G.; Lee, Seok Jae; Kim, Do Hyun; Park, Tae Jung

    2012-06-01

    Ultrasound-assisted synthesis of a graphene oxide (GO)-manganese oxide nanocomposite (GO-Mn3O4) was conducted without further modification of GO or employing secondary materials. With the GO nanoplate as a support, potassium permanganate oxidizes the carbon atoms in the GO support and gets reduced to Mn3O4. An intensive ultrasound method could reduce the number of reaction steps and temperature, enhance the reaction rate and furthermore achieve a Mn3O4 phase. The composite was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). The coverage and crystallinity of Mn3O4 were controlled by changing the ratio of permanganate to GO dispersion. The synthesized nanocomposite was used as a catalyst for poly(ethylene terephthalate) (PET) depolymerization into its monomer, bis(2-hydroxylethyl) terephthalate (BHET). The highest monomer yield of 96.4% was obtained with the nanocomposite containing the lowest amount of Mn3O4, while PET glycolysis with the Mn3O4 without GO yielded 82.7% BHET.Ultrasound-assisted synthesis of a graphene oxide (GO)-manganese oxide nanocomposite (GO-Mn3O4) was conducted without further modification of GO or employing secondary materials. With the GO nanoplate as a support, potassium permanganate oxidizes the carbon atoms in the GO support and gets reduced to Mn3O4. An intensive ultrasound method could reduce the number of reaction steps and temperature, enhance the reaction rate and furthermore achieve a Mn3O4 phase. The composite was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). The coverage and crystallinity of Mn3O4 were controlled by changing the ratio of permanganate to GO dispersion. The synthesized nanocomposite was used as a catalyst for poly(ethylene

  5. Enhancement of osseointegration of polyethylene terephthalate artificial ligament by coating of silk fibroin and depositing of hydroxyapatite

    PubMed Central

    Jiang, Jia; Wan, Fang; Yang, Jianjun; Hao, Wei; Wang, Yaxian; Yao, Jinrong; Shao, Zhengzhong; Zhang, Peng; Chen, Jun; Zhou, Liang; Chen, Shiyi

    2014-01-01

    Background Application of artificial ligament in anterior cruciate ligament reconstruction is one of the research focuses of sports medicine but the biological tendon–bone healing still remains a problem. The preliminary study of hydroxyapatite (HAP) coating on the polyethylene terephthalate (PET) surface could effectively induce the osteoblast differentiation, but the tendon–bone healing was still not stable. As a green synthesis process, the biomimetic mineralization can simulate the natural bone growth in vitro and in vivo. Methods HAP crystals were grown under the guide of silk fibroin (SF) PET surface by biomimetic route. Several techniques including scanning electron microscopy, attenuated total reflectance Fourier transform infrared spectroscopy, X-ray diffraction, and energy-dispersive X-ray spectroscopy were utilized for proving the introduction of both SF and HAP. The viability and osseointegration of bone marrow stromal cells on the surface of three kinds of ligament, including PET group (non-coating group), PET+SF group (SF-coating group), and PET+SF+HAP group (combined HAP- and SF-coating group), were analyzed by CCK-8 assays and alkaline phosphatase (ALP) detection. Seventy-two mature male New Zealand rabbits were randomly divided into three groups. Among them, 36 rabbits were sacrificed for mechanical testing, and histological examination for the others. Results The SF and SF+HAP were successfully coated on the surface of PET fiber. The CCK-8 assay showed that the cell proliferation on PET+SF+HAP group was better than the other two groups from 24 to 120 hours. After 14 days of culture, the cells in the PET+SF+HAP group delivered higher levels of ALP than the other two groups. After 3 days of culture, the expression level of integrin β1 in the PET+SF+HAP group and PET+SF group were higher than in the PET group. The mean load to failure and the stiffness value of the PET+SF+HAP group were both higher than the other two groups. Hematoxylin and

  6. Characterization of gamma-irradiated polyethylene terephthalate by liquid-chromatography mass-spectrometry (LC MS) with atmospheric-pressure chemical ionization (APCI)

    NASA Astrophysics Data System (ADS)

    Buchalla, Rainer; Begley, Timothy H.

    2006-01-01

    Low-molecular-weight (low-MW) constituents of polyethylene terephthalate (PET), irradiated with 60Co gamma rays at 25 and 50 kGy, were analyzed by HPLC-MS with atmospheric-pressure chemical ionization (APCI). Consistent with earlier results, the concentrations of the major compounds that are present in the non-irradiated PET do not change perceptibly. However, we find a small but significant increase in terephthalic acid ethylester, from less than 1 mg/kg in the non-irradiated control to ca. 2 mg/kg after 50 kGy, which has not been described before. The finding is important because it gives an impression of the sensitivity of the analytical method. Additionally, it shows that even very radiation-resistant polymers can form measurable amounts of low-MW radiolysis products. The potential and limitations of LC-MS for the analysis of radiolysis products and unidentified migrants are briefly discussed in the context of the question: How can we validate our analytical methods for unknown analytes?

  7. One-step sonochemical synthesis of a graphene oxide-manganese oxide nanocomposite for catalytic glycolysis of poly(ethylene terephthalate).

    PubMed

    Park, Gle; Bartolome, Leian; Lee, Kyoung G; Lee, Seok Jae; Kim, Do Hyun; Park, Tae Jung

    2012-07-01

    Ultrasound-assisted synthesis of a graphene oxide (GO)-manganese oxide nanocomposite (GO-Mn(3)O(4)) was conducted without further modification of GO or employing secondary materials. With the GO nanoplate as a support, potassium permanganate oxidizes the carbon atoms in the GO support and gets reduced to Mn(3)O(4). An intensive ultrasound method could reduce the number of reaction steps and temperature, enhance the reaction rate and furthermore achieve a Mn(3)O(4) phase. The composite was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). The coverage and crystallinity of Mn(3)O(4) were controlled by changing the ratio of permanganate to GO dispersion. The synthesized nanocomposite was used as a catalyst for poly(ethylene terephthalate) (PET) depolymerization into its monomer, bis(2-hydroxylethyl) terephthalate (BHET). The highest monomer yield of 96.4% was obtained with the nanocomposite containing the lowest amount of Mn(3)O(4), while PET glycolysis with the Mn(3)O(4) without GO yielded 82.7% BHET. PMID:22592889

  8. Interface and biocompatibility of polyethylene terephthalate knee ligament prostheses. A histological and ultrastructural device retrieval analysis in failed synthetic implants used for surgical repair of anterior cruciate ligaments.

    PubMed

    Kock, H J; Stürmer, K M; Letsch, R; Schmit-Neuerburg, K P

    1994-01-01

    In a prospective clinical study of 54 patients with acute anterior cruciate ligament instability, 56 artificial ligaments made of polyethylene terephthalate (Trevira hochfest) were implanted to restore knee stability. The average follow-up of these artificial knee ligaments was 40.2 (12-79) months; five implants (10%) had to be explanted due to failure after an average of 17.8 (6-50) months. All explants were examined by histological and ultrastructural methods in a device retrieval analysis. With regard to short- and medium-term artificial ligament failure in the human knee joint, a non-isometric surgical implantation technique, inappropriate strain during rehabilitation and implant fatigue and wear were responsible for ligament failures. PMID:7696041

  9. Transparent, flexible surface enhanced Raman scattering substrates based on Ag-coated structured PET (polyethylene terephthalate) for in-situ detection

    NASA Astrophysics Data System (ADS)

    Zuo, Zewen; Zhu, Kai; Gu, Chuan; Wen, Yibing; Cui, Guanglei; Qu, Jun

    2016-08-01

    Transparent, flexible surface-enhanced Raman scattering (SERS) substrates were fabricated by metalization of structured polyethylene terephthalate (PET) sheets. The resultant Ag-coated structured PET SERS substrates were revealed to be highly sensitive with good reproducibility and stability, an enhancement factor of 3 × 106 was acquired, which can be attributed mainly to the presence of plentiful multiple-type hot spots within the quasi-three-dimensional surface of the structured PET obtained by oxygen plasma etching. In addition, detections of model molecules on fruit skin were also carried out, demonstrating the great potential of the Ag-coated structured PET in in-situ detection of analyte on irregular objects. Importantly, the technique used for the preparation of such substrate is completely compatible with well-established silicon device technologies, and large-area fabrication with low cost can be readily realized.

  10. Structure and gas-barrier properties of amorphous hydrogenated carbon films deposited on inner walls of cylindrical polyethylene terephthalate by plasma-enhanced chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Li, Jing; Gong, Chunzhi; Tian, Xiubo; Yang, Shiqin; Fu, Ricky K. Y.; Chu, Paul K.

    2009-01-01

    The influence of radio-frequency (RF) power on the structure and gas permeation through amorphous hydrogenated carbon films deposited on cylindrical polyethylene terephthalate (PET) samples is investigated. The results show that a higher radio-frequency power leads to a smaller sp 3/sp 2 value but produces fewer defects with smaller size. The permeability of PET samples decreases significantly after a-C:H deposition and the RF only exerts a small influence. However, the coating uniformity, color, and wettability of the surface are affected by the RF power. A higher RF power results in to better uniformity and it may be attributed to the combination of the high-density plasma and sample heating.

  11. Grafting of copolymer styrene maleic anhydride on poly(ethylene terephthalate) film by chemical reaction and by plasma method: Optimization of the grafting reaction using experimental design

    NASA Astrophysics Data System (ADS)

    Bigan, Muriel; Bigot, Julien; Mutel, Brigitte; Coqueret, Xavier

    2008-02-01

    This work deals with the chemical grafting of a styrene maleic anhydride copolymer on the surface of a previously hydrolyzed polyethylene terephthalate (PET) film 12 μm thick via covalent bond. Two different ways are studied. The first one involves an activation of the hydrolyzed PET by the triethylamine before the grafting step. In the second one, the copolymer reacts with the 4-dimethylaminopyridine in order to form maleinyl pyridinium salt which reacts with alcohol function of the hydrolyzed PET. Characterization and quantification of the grafting are performed by Fourier transform infrared spectroscopy. Factorial experiment designs are used to optimize the process and to estimate experimental parameters effects. The opportunity to associate the chemical process to a cold remote nitrogen plasma one is also examined.

  12. In-Situ Small-Angle X-Ray Scattering Study of Simple Shear Oriented Poly(ethylene Terephthalate) during Heating

    NASA Astrophysics Data System (ADS)

    Wang, Zhigang; Xia, Zhiyong; Hsiao, Benjamin; Sue, Hj; Han, Charles

    2002-03-01

    An equal channel angular extrusion (ECAE) process was used to prepare poly(ethylene terephthalate) samples with segmental lamellar orientations. In-situ small-angle X-ray scattering measurements were carried out to follow the structure changes during heating of sections of equal-channel-angular-extruded PET samples before and after the transition line. The total scattering power, fractions of anisotropic and isotropic scattering, orientation factors and long periods along the flow directions were obtained. The changes in these parameters revealed the processes of lamellar relaxation, recrystallization and melting during heating in specimens of different orientation and morphology. Acknowledgements. The financial support of this work is provided by a grant from NIST and NSF (DMR 0098104). The Advanced Polymers Beamline is supported by DOE (DE-FG02-99ER 45760).

  13. Hemocompatibility improvement of poly(ethylene terephthalate) via self-polymerization of dopamine and covalent graft of zwitterions.

    PubMed

    Cai, Xianmei; Yuan, Jiang; Chen, Shuangchun; Li, Pengfei; Li, Li; Shen, Jian

    2014-03-01

    Poly (ethylene terephthalate) (PET) has been widely adopted as a scaffold biomaterial, but further hemocompatibility improvement is still needed for wide biomedical applications. Inspired by the composition of adhesive proteins in mussels, we propose to use self-polymerized dopamine to form a surface-adherent polydopamine layer onto PET sheet, followed by Michael addition with N,N-dimethylethylenediamine (DMDA) to build tertiary amine, and final zwitterions(sulfobetaine and carboxybetaine) construction through ring-opening reaction. Physicochemical properties of substrates were demonstrated by water contact angle measurement, attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS). The hemocompatibility was evaluated by platelet adhesion, hemolytic, and protein adsorption. The results showed that the zwitterions immobilized PET endowed with improved resistance to nonspecific protein adsorption and platelet adhesion as well as nonhemolytic. The zwitterions with desirable hemocompatibility can be readily tailored to catheter for various biomedical applications. PMID:24433885

  14. Morphological and Chemical Evolution of Gradually Deposited Diamond-Like Carbon Films on Polyethylene Terephthalate: From Subplantation Processes to Structural Reorganization by Intrinsic Stress Release Phenomena.

    PubMed

    Catena, Alberto; Guo, Qiaochu; Kunze, Michael R; Agnello, Simonpietro; Gelardi, Franco M; Wehner, Stefan; Fischer, Christian B

    2016-04-27

    Diamond-like carbon (DLC) films on polyethylene terephthalate (PET) are nowadays intensively studied composites due to their excellent gas barrier properties and biocompatibility. Despite their applicative features being highly explored, the interface properties and structural film evolution of DLC coatings on PET during deposition processes are still sparsely investigated. In this study two different types of DLC films were gradually deposited on PET by radio frequency plasma-enhanced chemical vapor deposition (RF-PECVD) using acetylene plasma. The surface morphology of the deposited samples has been analyzed by atomic force microscopy (AFM). Their chemical composition was investigated by diffusive reflectance infrared Fourier transform (DRIFT) and Raman spectroscopy analysis and the surface wettability by contact angle measurements. Subplantation processes and interface effects are revealed through the morphological and chemical analysis of both types. During plasma deposition processes the increasing carbon load causes the rise of intrinsic film stress. It is proven that stress release phenomena cause the transition between polymer-like to a more cross-linked DLC network by folding dehydrogenated chains into closed 6-fold rings. These findings significantly lead to an enhanced understanding in DLC film growth mechanism by RF-PECVD processes. PMID:27058762

  15. Disposal of post-consumer polyethylene terephthalate (PET) bottles: comparison of five disposal alternatives in the small island state of Mauritius using a life cycle assessment tool.

    PubMed

    Foolmaun, Rajendra Kumar; Ramjeeawon, Toolseeram

    2012-01-01

    Used polyethylene terephthalate bottles (PET) dumped indiscriminately onto bare lands and water bodies constitute an eyesore. This problem is viewed as a serious impediment to the flourishing tourism industry in Mauritius. Currently, over 100 million PET bottles are generated annually and the only fully operational disposal route is through the sole sanitary landfill. There is no formal segregation of waste and therefore used PET bottles are disposed of commingled with domestic waste. Despite a satisfactory waste collection system, a considerable amount of used PET bottles unfortunately end up in water bodies and on bare lands. An appreciable amount of PET bottles is now being collected separately for flake production prior to export to South Africa. This paper investigated the environmental impact of five waste management scenarios (100% landfill; 100% incineration with energy recovery; 50% incineration and 50% landfill; 34% flake production and 66% landfill; 100% flake production) for used PET bottles in Mauritius. Comparison of the five scenarios was based on the life cycle assessment (LCA) methodology described in ISO 14040 and ISO 14044. SimaPro 7.1 software was used to analyse the data. Comparison of the five scenarios showed that the highest environmental impacts occurred when 100% of used PET bottles were sent to the landfill. The comparison also indicated that there were least impacts on the environment when all used PET bottles were incinerated with energy recovery. PMID:22629630

  16. Effects of storage temperature and duration on release of antimony and bisphenol A from polyethylene terephthalate drinking water bottles of China.

    PubMed

    Fan, Ying-Ying; Zheng, Jian-Lun; Ren, Jing-Hua; Luo, Jun; Cui, Xin-Yi; Ma, Lena Q

    2014-09-01

    We investigated effects of storage temperature and duration on release of antimony (Sb) and bisphenol A (BPA) from 16 brands of polyethylene terephthalate (PET) drinking water bottles in China. After 1-week storage, Sb release increased from 1.88-8.32 ng/L at 4 °C, to 2.10-18.4 ng/L at 25 °C and to 20.3-2604 ng/L at 70 °C. The corresponding releases for BPA were less at 0.26-18.7, 0.62-22.6, and 2.89-38.9 ng/L. Both Sb and BPA release increased with storage duration up to 4-week, but their releasing rates decreased with storage time, indicating that Sb and BPA release from PET bottles may become stable under long term storage. Human health risk was evaluated based on the worst case, i.e., storage at 70 °C for 4-week. Chronic daily intake (CDI) caused by BPA release was below USEPA regulation, Sb release in one brand exceeded USEPA regulated CDI (400 ng/kg bw/d) with values of 409 and 1430 ng/kg bw/d for adult and children. PMID:24907857

  17. Effects of Defects in SiO2 Thin Films Prepared on Polyethylene Terephthalate by High-Temperature E-beam Deposition

    NASA Astrophysics Data System (ADS)

    Han, Jin‑Woo; Kang, Hee‑Jin; Kim, Jong‑Hwan; Seo, Dae‑Shik

    2006-08-01

    In this study, we characterized silicon oxide (SiO2) thin film prepared on polyethylene terephthalate (PET) substrates by electron-beam (e-beam) deposition for transparent barrier application. As the chamber temperature is increased from 30 to 110 °C, the roughness increases while water vapor transmission rate (WVTR) decreases. Under these conditions, WVTR of PET can be reduced from a level of 0.57 g/m2/day (bare subtrate) to 0.05 g/m2/day after application of a 200-nm-thick SiO2 coating at 110 °C. A more efficient way to improve permeation of PET was carried out by using a double sided coating of a 5-μm-thick parylene film. It was found that WVTR for PET substrates can be reduced to a level of -0.2 g/m2/day. The double-sided parylene coating on PET could contribute in lowering the stress of oxide film, which greatly improves the WVTR data. These results indicate that the SiO2/parylene/PET barrier coatings have a high potential for flexible organic light-emitting diode (OLED) applications.

  18. Electrical properties and surface morphology of electron beam evaporated p-type silicon thin films on polyethylene terephthalate for solar cells applications

    SciTech Connect

    Ang, P. C.; Ibrahim, K.; Pakhuruddin, M. Z.

    2015-04-24

    One way to realize low-cost thin film silicon (Si) solar cells fabrication is by depositing the films with high-deposition rate and manufacturing-compatible electron beam (e-beam) evaporation onto inexpensive foreign substrates such as glass or plastic. Most of the ongoing research is reported on e-beam evaporation of Si films on glass substrates to make polycrystalline solar cells but works combining both e-beam evaporation and plastic substrates are still scarce in the literature. This paper studies electrical properties and surface morphology of 1 µm electron beam evaporated Al-doped p-type silicon thin films on textured polyethylene terephthalate (PET) substrate for application as an absorber layer in solar cells. In this work, Si thin films with different doping concentrations (including an undoped reference) are prepared by e-beam evaporation. Energy dispersion X-ray (EDX) showed that the Si films are uniformly doped by Al dopant atoms. With increased Al/Si ratio, doping concentration increased while both resistivity and carrier mobility of the films showed opposite relationships. Root mean square (RMS) surface roughness increased. Overall, the Al-doped Si film with Al/Si ratio of 2% (doping concentration = 1.57×10{sup 16} atoms/cm{sup 3}) has been found to provide the optimum properties of a p-type absorber layer for fabrication of thin film Si solar cells on PET substrate.

  19. Effects of different laser and plasma treatments on the interface and adherence between evaporated aluminium and polyethylene terephthalate films: X-ray photoemission, and adhesion studies

    NASA Astrophysics Data System (ADS)

    Ardelean, H.; Petit, S.; Laurens, P.; Marcus, P.; Arefi-Khonsari, F.

    2005-04-01

    Chemical functionalities, topography and adherence between Al and polyethylene terephthalate (PET) films, modified by laser treatment below the polymer ablation threshold fluence in air and in helium at different wavelengths, fluences, pulse numbers and by low pressure plasma treatment in He 95% with O 2 5%, at 0.2 W/cm 3 were investigated by XPS, AFM, water contact angle and adhesion measurements. XPS results revealed (i) formation of polar-oxygenated functional groups (C dbnd O, O sbnd C dbnd O) by laser treatments in air and (ii) incorporation of ester and ether groups by plasma treatment in He 95% with O 2 5%. After deposition of thermally evaporated Al on laser or plasma treated PET films, U-Peel tests indicated that laser treatment in air at 248 nm and 20 mJ/cm 2, and plasma treatment improved Al/PET adhesion. XPS studies revealed the presence of an increasing number of Al sbnd O sbnd C stable and cohesive interfacial complexes formed by chemical interaction between aluminium and the laser treated in air or plasma treated in He 95% with O 2 5% PET films. These interfacial compounds play an important role in the enhancement of the metal/polymer adhesion.

  20. Effect of Biaxial Stretching at Temperatures and Strain Histories Comparable to Injection Stretch Blow Moulding on Tensile Modulus for Polyethylene Terephthalate (PET)

    NASA Astrophysics Data System (ADS)

    Tan, C. W.; Menary, G. H.; Harkin-Jones, E. M. A.; Armstrong, C. G.; Martin, P. J.

    2007-04-01

    This study is particularly relevant to the injection stretch blow moulding (ISBM) process where PET material is typically biaxially stretched to form bottles for the water and carbonated soft drinks industry. The aim of this paper is to investigate the effect of biaxial stretching on the mechanical properties of Polyethylene Terephthalate (PET) using a custom built biaxial testing machine. An initially amorphous PET sample was prepared via injection moulding to form a square sample (76mm × 76mm) suitable for stretching on the machine. This sample was then subjected to a series of biaxial tests (simultaneous and sequential) within a temperature range between 85°C and 110 °C, strain rates in the range of 1s-1 to 32s-1 and stretch ratios in the range of 1.5 to 3. Specimens were subsequently cut from the biaxial stretched sheets and used to measure the tensile modulus. Results showed that there is almost no effect found for strain rate and temperature on modulus development whilst stretch ratio and mode of deformation played the most important role on modulus development on PET under biaxial deformation.

  1. A disulfide bridge in the calcium binding site of a polyester hydrolase increases its thermal stability and activity against polyethylene terephthalate.

    PubMed

    Then, Johannes; Wei, Ren; Oeser, Thorsten; Gerdts, André; Schmidt, Juliane; Barth, Markus; Zimmermann, Wolfgang

    2016-05-01

    Elevated reaction temperatures are crucial for the efficient enzymatic degradation of polyethylene terephthalate (PET). A disulfide bridge was introduced to the polyester hydrolase TfCut2 to substitute its calcium binding site. The melting point of the resulting variant increased to 94.7 °C (wild-type TfCut2: 69.8 °C) and its half-inactivation temperature to 84.6 °C (TfCut2: 67.3 °C). The variant D204C-E253C-D174R obtained by introducing further mutations at vicinal residues showed a temperature optimum between 75 and 80 °C compared to 65 and 70 °C of the wild-type enzyme. The variant caused a weight loss of PET films of 25.0 ± 0.8% (TfCut2: 0.3 ± 0.1%) at 70 °C after a reaction time of 48 h. The results demonstrate that a highly efficient and calcium-independent thermostable polyester hydrolase can be obtained by replacing its calcium binding site with a disulfide bridge. PMID:27419048

  2. The effect of polystyrene sodium sulfonate grafting on polyethylene terephthalate artificial ligaments on in vitro mineralisation and in vivo bone tissue integration.

    PubMed

    Vaquette, Cédryck; Viateau, Véronique; Guérard, Sandra; Anagnostou, Fani; Manassero, Mathieu; Castner, David G; Migonney, Véronique

    2013-09-01

    This study investigates the impact of polystyrene sodium sulfonate (PolyNaSS) grafting onto the osseo-integration of a polyethylene terephthalate artificial ligament (Ligament Advanced Reinforcement System, LARS™) used for Anterior Cruciate Ligament (ACL). The performance of grafted and non-grafted ligaments was assessed in vitro by culturing human osteoblasts under osteogenic induction and this demonstrated that the surface modification was capable of up-regulating the secretion of ALP and induced higher level of mineralisation as measured 6 weeks post-seeding by Micro-Computed Tomography. Grafted and non-grafted LARS™ were subsequently implanted in an ovine model for ACL reconstruction and the ligament-to-bone interface was evaluated by histology and biomechanical testings 3 and 12 months post-implantation. The grafted ligaments exhibited more frequent direct ligament-to-bone contact and bone formation in the core of the ligament at the later time point than the non-grafted specimens, the grafting also significantly reduced the fibrous encapsulation of the ligament 12 months post-implantation. However, this improved osseo-integration was not translated into a significant increase in the biomechanical pull-out loads. These results provide evidences that PolyNaSS grafting improved the osseo-integration of the artificial ligament within the bone tunnels. This might positively influence the outcome of the surgical reconstructions, as higher ligament stability is believed to limit micro-movement and therefore permits earlier and enhanced healing. PMID:23790438

  3. The Use of Elasto-Visco-Plastic Material Model Coupled with Pressure-Volume Thermodynamic Relationship to Simulate the Stretch Blow Molding of Polyethylene Terephthalate

    NASA Astrophysics Data System (ADS)

    Mir, H.; Benrabah, Z.; Thibault, F.

    2007-05-01

    The use of polyethylene terephthalate (PET) in the stretch blow molding process presents several challenging issues due to various processing parameters and complex behavior of the material, which is both temperature and strain-rate dependent. In this paper, we generalize the G'Sell-Jonas law in 3D to model and simulate the elasto-visco-plastic (EVP) behavior of PET, taking into account strain-hardening and strain-softening. It is observed that the internal pressure (inside the preform) is significantly different from the nominal pressure (imposed in the blowing device upstream) since the internal pressure and the enclosed volume of the preform are fully coupled. In order to accurately simulate this phenomenon, a thermodynamic model was used to characterize the pressure-volume relationship (PVR). The predicted pressure evolution is thus more realistic when imposing only the machine power of the blowing device (air compressor or vacuum pump). Mechanical and temperature equilibrium equations are fully nonlinear and solved separately with implicit schemes on the current deformed configuration, which is updated at each time step. Biaxial characterization tests were used to determine the model parameters in order to simulate the stretch blow molding process using the pressure-volume thermodynamic relationship. To validate this model, thickness predictions for three industrial cases will be presented and compared to experimental measurements.

  4. Radiation induced graft copolymerization of n-butyl acrylate onto poly(ethylene terephthalate) (PET) films and thermal properties of the obtained graft copolymer

    NASA Astrophysics Data System (ADS)

    Ping, Xiang; Wang, Mozhen; Ge, Xuewu

    2011-05-01

    n-Butyl acrylate (BA) was successfully grafted onto poly(ethylene terephthalate) (PET) film using simultaneous radiation induced graft copolymerization with gamma rays. When BA concentration ranges from 20% to 30%, the Degree of Grafting (DG), measured by gravimetry and 1H NMR, increases with the monomer concentration and absorbed dose, but decreases with dose rate from 0.83 to 2.53 kGy/h. The maximum DG can reach up to 22.1%. The thermal transition temperatures such as glass-transition temperature ( Tg) and cold-crystallization temperature ( Tcc) of PET in grafted films were little different from those in original PET film, indicating that microphase separation occurred between PBA side chains and PET backbone. This work implied that if PET/elastomers (e.g., acrylate rubber) blends are radiated by high energy gamma rays under a certain condition, PET-g-polyacrylate copolymer may be produced in-situ, which will improve the compatibility between PET and the elastomers so as to improve the integral mechanical properties of PET based engineering plastic.

  5. Electrical properties and surface morphology of electron beam evaporated p-type silicon thin films on polyethylene terephthalate for solar cells applications

    NASA Astrophysics Data System (ADS)

    Ang, P. C.; Ibrahim, K.; Pakhuruddin, M. Z.

    2015-04-01

    One way to realize low-cost thin film silicon (Si) solar cells fabrication is by depositing the films with high-deposition rate and manufacturing-compatible electron beam (e-beam) evaporation onto inexpensive foreign substrates such as glass or plastic. Most of the ongoing research is reported on e-beam evaporation of Si films on glass substrates to make polycrystalline solar cells but works combining both e-beam evaporation and plastic substrates are still scarce in the literature. This paper studies electrical properties and surface morphology of 1 µm electron beam evaporated Al-doped p-type silicon thin films on textured polyethylene terephthalate (PET) substrate for application as an absorber layer in solar cells. In this work, Si thin films with different doping concentrations (including an undoped reference) are prepared by e-beam evaporation. Energy dispersion X-ray (EDX) showed that the Si films are uniformly doped by Al dopant atoms. With increased Al/Si ratio, doping concentration increased while both resistivity and carrier mobility of the films showed opposite relationships. Root mean square (RMS) surface roughness increased. Overall, the Al-doped Si film with Al/Si ratio of 2% (doping concentration = 1.57×1016 atoms/cm3) has been found to provide the optimum properties of a p-type absorber layer for fabrication of thin film Si solar cells on PET substrate.

  6. Two Novel Class II Hydrophobins from Trichoderma spp. Stimulate Enzymatic Hydrolysis of Poly(Ethylene Terephthalate) when Expressed as Fusion Proteins

    PubMed Central

    Espino-Rammer, Liliana; Ribitsch, Doris; Przylucka, Agnieszka; Marold, Annemarie; Greimel, Katrin J.; Herrero Acero, Enrique; Guebitz, Georg M.; Kubicek, Christian P.

    2013-01-01

    Poly(ethylene terephthalate) (PET) can be functionalized and/or recycled via hydrolysis by microbial cutinases. The rate of hydrolysis is however low. Here, we tested whether hydrophobins (HFBs), small secreted fungal proteins containing eight positionally conserved cysteine residues, are able to enhance the rate of enzymatic hydrolysis of PET. Species of the fungal genus Trichoderma have the most proliferated arsenal of class II hydrophobin-encoding genes among fungi. To this end, we studied two novel class II HFBs (HFB4 and HFB7) of Trichoderma. HFB4 and HFB7, produced in Escherichia coli as fusions to the C terminus of glutathione S-transferase, exhibited subtle structural differences reflected in hydrophobicity plots that correlated with unequal hydrophobicity and hydrophily, respectively, of particular amino acid residues. Both proteins exhibited a dosage-dependent stimulation effect on PET hydrolysis by cutinase from Humicola insolens, with HFB4 displaying an adsorption isotherm-like behavior, whereas HFB7 was active only at very low concentrations and was inhibitory at higher concentrations. We conclude that class II HFBs can stimulate the activity of cutinases on PET, but individual HFBs can display different properties. The present findings suggest that hydrophobins can be used in the enzymatic hydrolysis of aromatic-aliphatic polyesters such as PET. PMID:23645195

  7. Contaminants and levels of occurrence in washed and shredded poly(ethylene terephthalate) from curbside collection. II: Validation of extraction procedures, particle size sampling and crystallinity.

    PubMed

    Konkol, L M; Cross, R F; Harding, I H; Kosior, E

    2003-10-01

    Part I of this study showed that washed and dried, shredded poly(ethylene terephthalate) (PET) (flake) obtained from curbside collection when Soxhlet extracted contained 26 semivolatile contaminants below the US FDA threshold of 215 ppb and six above this level. This paper reports the validation of the Soxhlet extraction technique by comparison with total dissolution with trifluoroacetic acid (TFA). The work was carried out for two of the three particle size ranges obtained by grinding the PET flake (300-425 and 425-700 microm) and for the unground flake. Further validation was undertaken by comparison of contaminant levels determined by total dissolution with TFA and sonication with dichloromethane (DCM) using flake ground to the 0-300 microm size range. The levels of contaminants increased with decreasing particle size range, but X-ray diffraction measurements of degrees of crystallinity were similar for each PET particle size range, thus showing that the differences in contaminant levels were not due to variable percentages of the amorphous material from the tops and bottoms of shredded bottles, relative to the amounts of crystalline PET from the mid-sections of the bottles. Hence, it was postulated that the variations in contaminant levels were due to selective grinding of the more highly contaminated surfaces, whilst the larger particles incorporated the less contaminated interior material. The grinding was also strongly selective with respect to the amorphous flake. Analysis of the segregated amorphous and crystalline flake phases indicated that many contaminants were similarly absorbed into both phases, whilst some were preferred by the amorphous PET and others were preferred by the crystalline PET. PMID:14594681

  8. Facile and efficient poly(ethylene terephthalate) fibers-in-tube for online solid-phase microextraction towards polycyclic aromatic hydrocarbons.

    PubMed

    Bu, Yanan; Feng, Juanjuan; Sun, Min; Zhou, Changli; Luo, Chuannan

    2016-07-01

    Poly(ethylene terephthalate) (polyester) fibers as solid-phase microextraction (SPME) adsorbent were directly filled in a poly(ether ether ketone) (PEEK) tube, for online analysis of polycyclic aromatic hydrocarbons (PAHs) in environmental water samples, coupled with high-performance liquid chromatography. The facile, economic, and environmental polyester fibers-in-tube SPME device exhibited high extraction efficiency, good selectivity for PAHs, and satisfactory durability. Under optimum conditions, the polyester fibers provided satisfactory enhancement factors in the range of 307-1646, and low detection limits ranging from 0.01 to 0.03 μg L(-1). The linearity was in the range of 0.03-80 μg L(-1) with correlation coefficients (r) ranging from 0.9978 to 0.9997. Limit of quantification was defined as a concentration of the analytes with a ten-time signal-to-noise ratio (S/N = 10) and was in the range of 0.03-0.1 μg L(-1). The intra-day and inter-day precisions for quantitative analysis were investigated and the relative standard deviation (RSD) was lower than 5.8 and 6.9 %, respectively. Extraction repeatability was also investigated and its RSD was in the range of 3.8-7.8 %. Finally, the fiber-in-tube SPME device was successfully applied to analyze PAHs in water samples. Graphical abstract Schematic diagrams of polyester fibers-in-tube device and the automated in-tube SPME-HPLC system. PMID:27173390

  9. Development of an LC-MS/MS method for studying migration characteristics of acetaldehyde in polyethylene terephthalate (PET)-packed mineral water.

    PubMed

    Baumjohann, Nina; Harms, Diedrich

    2015-01-01

    During storage, acetaldehyde migration from polyethylene terephthalate (PET) bottles can affect the quality of mineral water even in the low µg l(-1) range negatively, as it features a fruity or plastic-like off-flavour. For a sensitive and fast analysis of acetaldehyde in mineral water, a new analysis method of 2,4-dinitrophenylhydrazine (DNPH) derivatisation followed by HPLC-electrospray tandem mass spectrometry (ESI-MS/MS) was developed. Acetaldehyde was directly derivatised in the mineral water sample avoiding extraction and/or pre-concentration steps and then analysed by reversed-phase HPLC-ESI-MS/MS using multiple reaction monitoring mode (MRM). Along with method development, the optimum molar excess of DNPH in contrast to acetaldehyde was studied for the mineral water matrix, because no specific and robust data were yet available for this critical parameter. Best results were obtained by using a calibration via the derivatisation reaction. Without any analyte enrichment or extraction, an LOD of 0.5 µg l(-1) and an LOQ of 1.9 µg l(-1) were achieved. Using the developed method, mineral water samples packed in PET bottles from Germany were analysed and the correlation between the acetaldehyde concentration and other characteristics of the samples was evaluated illustrating the applicability of the method. Besides a relationship between bottle size and CO2 content of the mineral water and acetaldehyde migration, a correlation with acetaldehyde migration and the material composition of the bottle, e.g. recycled PET, was noted. Investigating the light influence on the acetaldehyde migration with a newly developed, reproducible light exposure setup, a significant increase of the acetaldehyde concentration in carbonated mineral water samples was observed. PMID:26258902

  10. Development of thrombus-resistant and cell compatible crimped polyethylene terephthalate cardiovascular grafts using surface co-immobilized heparin and collagen.

    PubMed

    Al Meslmani, Bassam; Mahmoud, Gihan; Strehlow, Boris; Mohr, Eva; Leichtweiß, Thomas; Bakowsky, Udo

    2014-10-01

    Short-term patency of polyethylene terephthalate (PET) cardiovascular grafts is determined mainly by the inherent thrombogenicity and improper endothelialization following grafts implantation. The aim of the present study was to immobilize heparin to develop thrombus resistant grafts. Additionally, collagen was co-immobilized to enhance the host cell compatibility. The synthetic woven and knitted forms of crimped PET grafts were surface modified by Denier reduction to produce functional carboxyl groups. The produced groups were used as anchor sites for covalent immobilization of heparin or co-immobilization of heparin/collagen by the end-point method. The modified surface was characterized using Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The biological activity of immobilized molecules was investigated in vitro using direct blood coagulation test, and "platelet deposition under flow condition. Furthermore, the biocompatibility of modified grafts with host cells was assessed using L929 cell as model. All modified grafts showed significant resistance against fibrin and clot formation. The number of deposited platelets on heparin-immobilized woven and knitted grafts obviously decreased by 3 fold and 2.8 fold per unit surface area respectively, while the heparin/collagen co-immobilized grafts showed only a decrease by 1.7 and 1.8 fold compared to unmodified PET. Heparin-immobilized grafts reported no significant effect on L929 cells adhesion and growth (P>0.05), conversely, collagen co-immobilization considerably increased cell adhesion almost ~1.3 fold and 2 fold per unit surface area for woven and knitted grafts respectively. Our results emphasize that immobilization of heparin minimized the inherent thrombogenicity of the PET grafts. The simultaneous co-immobilization of collagen supported host cell adhesion and growth required for the grafts biocompatibility. PMID:25175248

  11. An XPS study on the chemical bond structure at the interface between SiO{sub x}N{sub y} and N doped polyethylene terephthalate

    SciTech Connect

    Ding Wanyu; Li Li; Zhang Lina; Chai Weiping; Ju Dongying; Peng Shou

    2013-03-14

    The super-thin silicon oxynitride (SiO{sub x}N{sub y}) films were deposited onto the N doped polyethylene terephthalate (PET) surface. Varying the N doping parameters, the different chemical bond structures were obtained at the interface between the SiO{sub x}N{sub y} film and the PET surface. X-ray photoelectron spectra results showed that at the initial stage of SiO{sub x}N{sub y} film growth, the C=N bonds could be broken and C-N-Si crosslink bonds could be formed at the interface of SiO{sub x}N{sub y}/PET, which C=N bonds could be formed onto the PET surface during the N doping process. At these positions, the SiO{sub x}N{sub y} film could be crosslinked well onto the PET surface. Meanwhile, the doped N could crosslink the [SiO{sub 4}] and [SiN{sub 4}] tetrahedrons, which could easily form the dense layer structure at the initial stage of SiO{sub x}N{sub y} film growth, instead of the ring and/or chain structures of [SiO{sub 4}] tetrahedrons crosslinked by O. Finally, from the point of applying SiO{sub x}N{sub y}/PET complex as the substrate, the present work reveals a simple way to crosslink them, as well as the crosslink model and physicochemical mechanism happened at the interface of complex.

  12. AFM probing of polymer/nanofiller interfacial adhesion and its correlation with bulk mechanical properties in a poly(ethylene terephthalate) nanocomposite.

    PubMed

    Aoyama, Shigeru; Park, Yong Tae; Macosko, Christopher W; Ougizawa, Toshiaki; Haugstad, Greg

    2014-11-01

    The interfacial adhesion between polymer and nanofiller plays an important role in affecting the properties of nanocomposites. The detailed relationship between interfacial adhesion and bulk properties, however, is unclear. In this work, we developed an atomic force microscopy (AFM)-based abrasive scanning methodology, as applied to model laminate systems, to probe the strength of interfacial adhesion relevant to poly(ethylene terephthalate) (PET)/graphene or clay nanocomposites. Graphite and mica substrates covered with ∼2 nm thick PET films were abrasively sheared by an AFM tip as a model measurement of interfacial strength between matrix PET and dispersed graphene and clay, respectively. During several abrasive raster-scan cycles, PET was shear-displaced from the scanned region. At temperatures below the PET glass transition, PET on graphite exhibited abrupt delamination (i.e., full adhesive failure), whereas PET on mica did not; rather, it exhibited a degree of cohesive failure within the shear-displaced layer. Moreover, 100-fold higher force scanning procedures were required to abrade through an ultimate "precursor" layer of PET only ∼0.2-0.5 nm thick, which must be largely disentangled from the matrix polymer. Thus, the adhesive interface of relevance to the strength of clay-filler nanocomposites is between matrix polymer and strongly bound polymer. At 90 °C, above the bulk PET glass transition temperature, the PET film exhibited cohesive failure on both graphite and mica. Our results suggest that there is little difference in the strength of the relevant interfacial adhesion in the two nanocomposites within the rubbery dynamic regime. Further, the bulk mechanical properties of melt mixed PET/graphene and PET/clay nanocomposites were evaluated by dynamic mechanical analysis. The glassy dynamic storage modulus of the PET/clay nanocomposite was higher than that of PET/graphene, correlating with the differences in interfacial adhesion probed by AFM. PMID

  13. Local delivery of controlled-release simvastatin to improve the biocompatibility of polyethylene terephthalate artificial ligaments for reconstruction of the anterior cruciate ligament.

    PubMed

    Zhang, Peng; Han, Fei; Li, Yunxia; Chen, Jiwu; Chen, Tianwu; Zhi, Yunlong; Jiang, Jia; Lin, Chao; Chen, Shiyi; Zhao, Peng

    2016-01-01

    The Ligament Advanced Reinforcement System has recently been widely used as the primary graft of choice in anterior cruciate ligament (ACL) reconstruction. But the biological graft-bone healing still remains a problem. Previous studies have shown that simvastatin (SIM) stimulates bone formation. The objective of this study was to investigate whether surface coating with collagen containing low-dose SIM microsphere could enhance the surface biocompatibility of polyethylene terephthalate (PET) artificial ligaments to accelerate graft-to-bone healing. The in vitro studies demonstrated that bone marrow stromal cells on the collagen-coated PET scaffolds (COL/PET) and simvastatin/collagen-coated PET scaffolds (SIM/COL/PET) proliferated vigorously. Compared with the PET group and the COL/PET group, SIM could induce bone marrow stromal cells' osteoblastic differentiation, high alkaline phosphatase activity, more mineralization deposition, and more expression of osteoblast-related genes, such as osteocalcin, runt-related transcription factor 2, bone morphogenetic protein-2, and vascular endothelial growth factor, in the SIM/COL/PET group. In vivo, rabbits received ACL reconstruction with different scaffolds. Histological analysis demonstrated that graft-bone healing was significantly greater with angiogenesis and osteogenesis in the SIM/COL/PET group than the other groups. In addition, biomechanical testing at the eighth week demonstrated a significant increase in the ultimate failure load and stiffness in the SIM/COL/PET group. The low dose of SIM-sustained release from SIM/COL/PET promoted the graft-bone healing via its effect on both angiogenesis and osteogenesis. This study suggested that collagen containing low-dose SIM microsphere coating on the surface of PET artificial ligaments could be potentially applied for ACL reconstruction. PMID:26869789

  14. Effects of Interphase Modification and Biaxial Orientation on Dielectric Properties of Poly(ethylene terephthalate)/Poly(vinylidene fluoride-co-hexafluoropropylene) Multilayer Films.

    PubMed

    Yin, Kezhen; Zhou, Zheng; Schuele, Donald E; Wolak, Mason; Zhu, Lei; Baer, Eric

    2016-06-01

    Recently, poly(vinylidene fluoride) (PVDF)-based multilayer films have demonstrated enhanced dielectric properties, combining high energy density and high dielectric breakdown strength from the component polymers. In this work, further enhanced dielectric properties were achieved through interface/interphase modulation and biaxial orientation for the poly(ethylene terephthalate)/poly(methyl methacrylate)/poly(vinylidene fluoride-co-hexafluoropropylene) [PET/PMMA/P(VDF-HFP)] three-component multilayer films. Because PMMA is miscible with P(VDF-HFP) and compatible with PET, the interfacial adhesion between PET and P(VDF-HFP) layers should be improved. Biaxial stretching of the as-extruded multilayer films induced formation of highly oriented fibrillar crystals in both P(VDF-HFP) and PET, resulting in improved dielectric properties with respect to the unstretched films. First, the parallel orientation of PVDF crystals reduced the dielectric loss from the αc relaxation in α crystals. Second, biaxial stretching constrained the amorphous phase in P(VDF-HFP) and thus the migrational loss from impurity ions was reduced. Third, biaxial stretching induced a significant amount of rigid amorphous phase in PET, further enhancing the breakdown strength of multilayer films. Due to the synergistic effects of improved interfacial adhesion and biaxial orientation, the PET/PMMA/P(VDF-HFP) 65-layer films with 8 vol % PMMA exhibited optimal dielectric properties with an energy density of 17.4 J/cm(3) at breakdown and the lowest dielectric loss. These three-component multilayer films are promising for future high-energy-density film capacitor applications. PMID:27163929

  15. Isolation of a Novel Cutinase Homolog with Polyethylene Terephthalate-Degrading Activity from Leaf-Branch Compost by Using a Metagenomic Approach

    PubMed Central

    Sulaiman, Sintawee; Yamato, Saya; Kanaya, Eiko; Kim, Joong-Jae; Koga, Yuichi; Takano, Kazufumi

    2012-01-01

    The gene encoding a cutinase homolog, LC-cutinase, was cloned from a fosmid library of a leaf-branch compost metagenome by functional screening using tributyrin agar plates. LC-cutinase shows the highest amino acid sequence identity of 59.7% to Thermomonospora curvata lipase. It also shows the 57.4% identity to Thermobifida fusca cutinase. When LC-cutinase without a putative signal peptide was secreted to the periplasm of Escherichia coli cells with the assistance of the pelB leader sequence, more than 50% of the recombinant protein, termed LC-cutinase*, was excreted into the extracellular medium. It was purified and characterized. LC-cutinase* hydrolyzed various fatty acid monoesters with acyl chain lengths of 2 to 18, with a preference for short-chain substrates (C4 substrate at most) most optimally at pH 8.5 and 50°C, but could not hydrolyze olive oil. It lost activity with half-lives of 40 min at 70°C and 7 min at 80°C. LC-cutinase* had an ability to degrade poly(ε-caprolactone) and polyethylene terephthalate (PET). The specific PET-degrading activity of LC-cutinase* was determined to be 12 mg/h/mg of enzyme (2.7 mg/h/μkat of pNP-butyrate-degrading activity) at pH 8.0 and 50°C. This activity is higher than those of the bacterial and fungal cutinases reported thus far, suggesting that LC-cutinase* not only serves as a good model for understanding the molecular mechanism of PET-degrading enzyme but also is potentially applicable for surface modification and degradation of PET. PMID:22194294

  16. Local delivery of controlled-release simvastatin to improve the biocompatibility of polyethylene terephthalate artificial ligaments for reconstruction of the anterior cruciate ligament

    PubMed Central

    Zhang, Peng; Han, Fei; Li, Yunxia; Chen, Jiwu; Chen, Tianwu; Zhi, Yunlong; Jiang, Jia; Lin, Chao; Chen, Shiyi; Zhao, Peng

    2016-01-01

    The Ligament Advanced Reinforcement System has recently been widely used as the primary graft of choice in anterior cruciate ligament (ACL) reconstruction. But the biological graft–bone healing still remains a problem. Previous studies have shown that simvastatin (SIM) stimulates bone formation. The objective of this study was to investigate whether surface coating with collagen containing low-dose SIM microsphere could enhance the surface biocompatibility of polyethylene terephthalate (PET) artificial ligaments to accelerate graft-to-bone healing. The in vitro studies demonstrated that bone marrow stromal cells on the collagen-coated PET scaffolds (COL/PET) and simvastatin/collagen-coated PET scaffolds (SIM/COL/PET) proliferated vigorously. Compared with the PET group and the COL/PET group, SIM could induce bone marrow stromal cells’ osteoblastic differentiation, high alkaline phosphatase activity, more mineralization deposition, and more expression of osteoblast-related genes, such as osteocalcin, runt-related transcription factor 2, bone morphogenetic protein-2, and vascular endothelial growth factor, in the SIM/COL/PET group. In vivo, rabbits received ACL reconstruction with different scaffolds. Histological analysis demonstrated that graft–bone healing was significantly greater with angiogenesis and osteogenesis in the SIM/COL/PET group than the other groups. In addition, biomechanical testing at the eighth week demonstrated a significant increase in the ultimate failure load and stiffness in the SIM/COL/PET group. The low dose of SIM-sustained release from SIM/COL/PET promoted the graft–bone healing via its effect on both angiogenesis and osteogenesis. This study suggested that collagen containing low-dose SIM microsphere coating on the surface of PET artificial ligaments could be potentially applied for ACL reconstruction. PMID:26869789

  17. European survey on post-consumer poly(ethylene terephthalate) (PET) materials to determine contamination levels and maximum consumer exposure from food packages made from recycled PET.

    PubMed

    Franz, R; Mauer, A; Welle, F

    2004-03-01

    Typical contamination and the frequency of misuse of poly(ethylene terephthalate) (PET) bottles are crucial parameters in the risk assessment of post-consumer recycled (PCR) PET intended for bottle-to-bottle recycling for direct food contact applications. Owing to the fact that misuse of PET bottles is a rare event, sustainable knowledge about the average concentration of hazardous compounds in PCR PET is accessible only by the screening of large numbers of samples. In order to establish average levels of contaminants in PET source materials for recycling, PET flakes from commercial washing plants (689 samples), reprocessed pellets (38) and super-clean pellets (217) were collected from 12 European countries between 1997 and 2001. Analysis of these materials by headspace gas chromatography revealed average and maximum levels in PCR PET of 18.6 and 86.0 mg kg-1 for acetaldehyde and 2.9 and 20 mg kg-1 for limonene, respectively. Acetaldehyde and limonene are typical compounds derived from PET itself and from prior PET bottle contents (flavouring components), respectively. Maximum levels in PCR PET of real contaminants such as misuse chemicals like solvents ranged from 1.4 to 2.7 mg kg-1, and statistically were shown to result from 0.03 to 0.04% of recollected PET bottles that had been misused. Based on a principal component analysis of the experimental data, the impact of the recollecting system and the European Union Member State where the post-consumer PET bottles had been collected on the nature and extent of adventitious contaminants was not significant. Under consideration of the cleaning efficiency of super-clean processes as well as migration from the bottle wall into food, it can be concluded that the consumer will be exposed at maximum to levels < 50 ng total misuse chemicals day-1. Therefore, PCR PET materials and articles produced by modern superclean technologies can be considered to be safe in direct food applications in the same way as virgin food

  18. Solid state structure and gas transport behavior of semicrystalline poly(ethylene terephthalate) and barrier coatings based on polyhydroxylated dendritic polymers

    NASA Astrophysics Data System (ADS)

    Lin, Jun

    The existence of rigid amorphous fraction (RAF) in semicrystalline poly(ethylene terephthalate) (PET) is associated with the lamellar stack crystalline morphology of this polymer, the regions where several crystalline lamellas are separated by very thin (20--40A) amorphous layers. In contrast, regular or mobile amorphous fraction (MAF) is associated with much thicker interstack regions. The specific volume of RAF in cold and melt crystallized PET was probed at 25°C using oxygen solubility measurements, and showed a direct correlation with the crystallization temperature. It was shown that upon crystallization from either melt or glassy state, RAF vitrifies at the crystallization temperature and resembles the glassy behavior despite high temperature. When cooled to room temperature, the RAF preserves a memory about the melt state of polymer, which is uniquely defined by the crystallization temperature. Consistent results were demonstrated by positron annihilation lifetime spectroscopy (PALS) study. Moreover, correlations between PALS and oxygen transport parameters suggested that the dominant free volume parameter which controls the diffusion process is the hole volume, whereas the dominant parameter controlling the solubility is the hole density. Oxygen transport properties were assessed for a series of hydroxyl-functional hyperbranched polyesters (HBPs) at both 0% and 50% relative humidity (RH). At 0% RH, all HBPs showed outstanding oxygen barrier properties, with the permeability coefficients more than one order magnitude smaller than that of the amorphous PET. It was found that the oxygen diffusion process was mainly determined by the free volume and characteristic jump length of gas molecules from one core to another core. On the other hand, the oxygen sorption was related with the glass transition temperature, following dual-sorption model. The different amount of volume fraction of periphery layers contributed to the difference in oxygen solubility among

  19. Migration measurement and modelling from poly(ethylene terephthalate) (PET) into soft drinks and fruit juices in comparison with food simulants.

    PubMed

    Franz, R; Welle, F

    2008-08-01

    Poly(ethylene terephthalate) (PET) bottles are widely used for beverages. Knowledge about the migration of organic compounds from the PET bottle wall into contact media is of interest especially when post-consumer recyclates are introduced into new PET bottles. Using migration theory, the migration of a compound can be calculated if the concentration in the bottle wall is known. On the other hand, for any given specific migration limit or maximum target concentration for organic chemical compounds in the bottled foodstuffs, the maximum allowable concentrations in the polymer CP,0 can be calculated. Since a food simulant cannot exactly simulate the real migration into the foodstuff or beverages, a worse-case simulation behaviour is the intention. However, if the migration calculation should not be too overestimative, the polymer-specific kinetic parameter for migration modelling, the so-called AP value, should be established appropriately. One objective of the study was the kinetic determination of the specific migration behaviour of low molecular weight compounds such as solvents with relatively high diffusion rates and, therefore, with high migration potential from the PET bottle wall into food simulants in comparison with real beverages. For this purpose, model contaminants were introduced into the bottle wall during pre-form production. The volatile compounds toluene and chlorobenzene were established at concentrations from about 20-30 mg kg(-1) to 300-350 mg kg(-1). Phenyl cyclohexane was present at concentrations of 35, 262 and 782 mg kg(-1), respectively. The low volatile compounds benzophenone and methyl stearate have bottle wall concentrations of about 100 mg kg(-1) in the low spiking level up to about 1000 mg kg(-1) in the highly spiked test bottle. From these experimental data, the polymer specific parameters (AP values) from mathematical migration modelling were derived. The experimental determined diffusing coefficients were determined, calculated and

  20. Fabricating metal-oxide-semiconductor field-effect transistors on a polyethylene terephthalate substrate by applying low-temperature layer transfer of a single-crystalline silicon layer by meniscus force

    SciTech Connect

    Sakaike, Kohei; Akazawa, Muneki; Nakamura, Shogo; Higashi, Seiichiro

    2013-12-02

    A low-temperature local-layer technique for transferring a single-crystalline silicon (c-Si) film by using a meniscus force was proposed, and an n-channel metal-oxide-semiconductor field-effect transistor (MOSFET) was fabricated on polyethylene terephthalate (PET) substrate. It was demonstrated that it is possible to transfer and form c-Si films in the required shape at the required position on PET substrates at extremely low temperatures by utilizing a meniscus force. The proposed technique for layer transfer was applied for fabricating high-performance c-Si MOSFETs on a PET substrate. The fabricated MOSFET showed a high on/off ratio of more than 10{sup 8} and a high field-effect mobility of 609 cm{sup 2} V{sup −1} s{sup −1}.

  1. Tissue engineering of fish skin: behavior of fish cells on poly(ethylene glycol terephthalate)/poly(butylene terephthalate) copolymers in relation to the composition of the polymer substrate as an initial step in constructing a robotic/living tissue hybrid.

    PubMed

    Pouliot, Roxane; Azhari, Rosa; Qanadilo, Hala F; Mahmood, Tahir A; Triantafyllou, Michael S; Langer, Robert

    2004-01-01

    This study presents the development of a biosynthetic fish skin to be used on aquatic robots that can emulate fish. Smoothness of the external surface is desired in improving high propulsive efficiency and maneuvering agility of autonomous underwater vehicles such as the RoboTuna (Triantafyllou, M., and Triantafyllou, G. Sci. Am. 272, 64, 1995). An initial step was to determine the seeding density and select a polymer for the scaffolds. The attachment and proliferation of chinook salmon embryo (CHSE-214) and brown bullhead (BB) cells were studied on different compositions of a poly(ethylene glycol terephthalate) (PEGT) and poly(butylene terephthalate) (PBT) copolymer (Polyactive). Polymer films were used, cast of three different compositions of PEGT/PBT (weight ratios of 55/45, 60/40, and 70/30) and two different molecular masses of PEGT (300 and 1000 Da). When a 55 wt% and a 300-Da molecular mass form of PEGT was used, maximum attachment and proliferation of CHSE-214 and BB cells were achieved. Histological studies and immunostaining indicate the presence of collagen and cytokeratins in the extracellular matrix formed after 14 days of culture. Porous scaffolds of PEGT/PBT copolymers were also used for three-dimensional tissue engineering of fish skin, using BB cells. Overall, our results indicate that fish cells can attach, proliferate, and express fish skin components on dense and porous Polyactive scaffolds. PMID:15009926

  2. Sequential pyrolysis of plastic to recover polystyrene HCL and terephthalic acid

    DOEpatents

    Evans, Robert J.; Chum, Helena L.

    1995-01-01

    A process of pyrolyzing plastic waste feed streams containing polyvinyl chloride, polyethylene terephthalate, polystyrene and polyethylene to recover polystyrene HCl and terephthalic acid comprising: heating the plastic waste feed stream to a first temperature; adding an acid or base catalyst on an oxide or carbonate support; heating the plastic waste feed stream to pyrolyze polyethylene terephthalate and polyvinyl chloride; separating terephthalic acid or HCl; heating to a second temperature to pyrolyze polystyrene; separating styrene; heating the waste feed stream to a third temperature to pyrolyze polyethylene; and separating hydrocarbons.

  3. Sequential pyrolysis of plastic to recover polystyrene, HCl and terephthalic acid

    DOEpatents

    Evans, R.J.; Chum, H.L.

    1995-11-07

    A process is described for pyrolyzing plastic waste feed streams containing polyvinyl chloride, polyethylene terephthalate, polystyrene and polyethylene to recover polystyrene, HCl and terephthalic acid comprising: heating the plastic waste feed stream to a first temperature; adding an acid or base catalyst on an oxide or carbonate support; heating the plastic waste feed stream to pyrolyze polyethylene terephthalate and polyvinyl chloride; separating terephthalic acid or HCl; heating to a second temperature to pyrolyze polystyrene; separating styrene; heating the waste feed stream to a third temperature to pyrolyze polyethylene; and separating hydrocarbons. 83 figs.

  4. Unusual Formation of Precursors for Crystallization of Ultra-High Performance Polypropylene and Poly(ethylene terephthalate) Fibers by Utilization of Ecologically Friendly Horizontal Isothermal Bath

    NASA Astrophysics Data System (ADS)

    Avci, Huseyin

    structural development and the production of ultra-high performance as-spun and drawn polypropylene (PP) filaments were investigated. Two different commercial fiber forming PP polymers were used with the melt flow rate of 4.1 and 36 g/10 min. The results demonstrate surprisingly different precursor morphologies for each type of polymer at their optimum process condition. Interestingly, the all treated fibers demonstrated the similar fiber performance having tenacity of about 7 g/d and modulus of 75 g/d for as-spun fibers. After fiber drawing with DR of 1.49, tenacity greater than 12 g/d and modulus higher than 190 g/d were observed. The mean value for the modulus after the drawing process for the high melt flow rate is about 196 g/d. The theoretical modulus of PP is 35--42 GPa17, 275-330 g/d, which demonstrates the hIB fiber's modulus performance is approaching its theoretical maximum values. A key aspect of the third section of this study was to obtain ultra-high performance poly(ethylene terephthalate) fibers (PET) by utilizing a low molecular weight polymer via hIB method. The resulted fibers showed the efficient polymer chain orientation and the highly crystalline and ordered structures. The highest tenacity of more than 8 and 10 g/d were observed for the as-spun and drawn fibers, respectively, after only 1.28 draw ratios. The significant effect of the temperature of hIB spinning system on the fibrillar structure and the precursor's formation of the as-spun fibers was demonstrated. The melting temperature increased 8.51 °C from 254.05 to 262.56 °C when untreated and treated fibers are compared. The most important contribution of this study is that all these various types of polymer precursors for crystallization with different molecular weights after the baths treatments were highly oriented, yet non-crystallized or just showed the initial stages of crystallization. By a subsequent hot drawing process with the low draw ratio (DR< 1.5), the treated fibers showed a well

  5. Evaporation-induced self-assembled silica colloidal particle-assisted nanoporous structural evolution of poly(ethylene terephthalate) nonwoven composite separators for high-safety/high-rate lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Lee, Jung-Ran; Won, Ji-Hye; Kim, Jong Hun; Kim, Ki Jae; Lee, Sang-Young

    2012-10-01

    A facile approach to the fabrication of nanoporous structure-tuned nonwoven composite separators is demonstrated for application in high-safety/high-rate lithium-ion batteries. This strategy is based on the construction of silica (SiO2) colloidal particle-assisted nanoporous structure in a poly(ethylene terephthalate) (PET) nonwoven substrate. The nanoparticle arrangement arising from evaporation-induced self-assembly of SiO2 colloidal particles allows the evolution of the unusual nanoporous structure, i.e. well-connected interstitial voids formed between close-packed SiO2 particles adhered by styrene-butadiene rubber (SBR) binders. Meanwhile, the PET nonwoven serves as a mechanical support that contributes to suppressing thermal shrinkage of the nonwoven composite separator. The aforementioned structural novelty of the nonwoven composite separator plays a key role in providing the separator with advantageous characteristics (specifically, good electrolyte wettability, high ionic conductivity, and benign compatibility with electrodes), which leads to the better cell performance than a commercialized polyethylene (PE) separator.

  6. Effect of Ar Ion Beam Pre-Treatment of Poly(ethylene terephthalate) Substrate on the Mechanical and Electrical Stability of Flexible InSnO Films Grown by Roll-to-Roll Sputtering System

    NASA Astrophysics Data System (ADS)

    Choi, Kwang-Hyuk; Kim, Han-Ki

    2013-10-01

    We investigated the effects of Ar ion beam irradiation on a flexible poly(ethylene terephthalate) (PET) substrate as surface pre-treatment method in the roll-to-roll (R2R) sputtering system and its contribution to the electrical durability of flexible InSnO (ITO) electrode upon that the flexible PET substrate under repeated mechanical stresses. It was found that the Ar ion beam irradiation of the flexible PET surface could improve an adhesion between R2R sputter-grown ITO film and the PET substrate. X-ray photoelectron spectroscopy results showed that the Ar ion beam irradiation lead to an increase of hydrophilic functional groups when the working pressure, Ar ion beam power, and exposure time increases. Repetitive bending stresses for the flexible ITO/PET film which fabricated through the surface pre-treatment by Ar ion beam irradiation showed more stable electrical durability than those of ITO films on the wet-cleaned PET substrate due to enhanced interfacial adhesion between the ITO film and PET surface. This suggests that the Ar ion beam pre-treatment before sputtering of ITO film in R2R sputtering system is an effective technique to improve the adhesion between ITO film and PET substrate.

  7. Exposure of the lysine in the gamma chain dodecapeptide of human fibrinogen is not enhanced by adsorption to poly(ethylene terephthalate) as measured by biotinylation and mass spectrometry.

    PubMed

    Ovod, Vitaliy; Scott, Evan A; Flake, Megan M; Parker, Stanley R; Bateman, Randall J; Elbert, Donald L

    2012-03-01

    Conformational changes in adsorbed fibrinogen may enhance the exposure of platelet adhesive sites that are inaccessible in solution. To test this hypothesis, mass spectrometric methods were developed to quantify chemical modification of lysine residues following adsorption of fibrinogen to biomaterials. The quantitative method used an internal standard consisting of isotope-labeled fibrinogen secreted by human HepG2 cells in culture. Lysine residues in the internal standard were partially reacted with NHS-biotin. For the experimental samples, normal human fibrinogen was adsorbed to poly(ethylene terephthalate) (PET) particles. The adsorbed fibrinogen was reacted with NHS-biotin and then eluted from the particles. Constant amounts of internal standard were added to sample fibrinogen and analyzed by liquid chromatography/tandem mass spectrometry. Biotinylation of the lysine residue in the platelet-adhesive gamma chain dodecapeptide (GCDP) was quantified by comparison with the internal standard. Approximately 80% of the GCDP peptides were biotinylated when fibrinogen was reacted with NHS-biotin in solution or adsorbed onto PET. These results are generally consistent with previous antibody binding studies and suggest that other regions of fibrinogen may be crucial in promoting platelet adhesion to materials. The results do not directly address but are consistent with the hypothesis that only activated platelets adhere to adsorbed fibrinogen. PMID:22213354

  8. Thresholds of Etchable Track Formation and Chemical Damage Parameters in Poly(ethylene terephthalate), Bisphenol A polycarbonate, and Poly(allyl diglycol carbonate) Films at the Stopping Powers Ranging from 10 to 12,000 keV/µm

    NASA Astrophysics Data System (ADS)

    Yamauchi, Tomoya; Mori, Yutaka; Morimoto, Akira; Kanasaki, Masato; Oda, Keiji; Kodaira, Satoshi; Konishi, Teruaki; Yasuda, Nakahiro; Tojo, Sachiko; Honda, Yoshihide; Barillon, Rémi

    2012-05-01

    The damage structure of latent tracks in poly(ethylene terephthalate) (PET) has been examined by Fourier transform infrared (FT-IR) measurements. Results are compared with those from previous studies on bisphenol A polycarbonate (PC) and poly(allyl diglycol carbonate) (PADC). These polymers are exposed to protons and heavy ions (He, C, Ne, Si, Ar, Fe, Kr, and Xe) in air with energies less than 6 MeV/n, as well as gamma rays from an intense Co-60 source. Chemical damage parameters, namely, damage density, which is the number of losses of considered functional groups per unit length of tracks, radial size of the track core, in which the considered chemical groups are lost, and radiation chemical yields (G values) for each group are evaluated as a function of the stopping power. It has been confirmed that latent tracks will be etchable when the radial track core size is larger than the distance between two adjacent breaking points of polymer chains. The predominant breaking points are the C-O bonds in ether, ester, and carbonate ester bonds.

  9. Layer-by-layer hyaluronic acid-chitosan coating promoted new collagen ingrowth into a poly(ethylene terephthalate) artificial ligament in a rabbit medical collateral ligament (MCL) reconstruction model.

    PubMed

    Li, Hong; Jiang, Jia; Ge, Yunsheng; Xu, Jialing; Zhang, Pengyun; Zhong, Wei; Chen, Shiyi

    2013-01-01

    The ideal artificial ligament graft should have favorable biocompatibility to facilitate cell adhesion, proliferation, and collagen regeneration. In this present study, surface modification was performed on a poly(ethylene terephthalate) (PET) artificial ligament graft by layer-by-layer (LBL) self-assembly coating of hyaluronic acid (HA) and chitosan (CS). The surface characterization of the ligament was examined using scanning electron microscopy, atomic force microscopy, and energy-dispersive X-ray spectroscopy. The results of in vitro culturing of human foreskin fibroblast cells supported the hypothesis that the LBL coating of CS-HA could promote the cell proliferation and adhesion on the sheets. A rabbit medical collateral ligament reconstruction model was used to evaluate the effect of this LBL coating in vivo. The final results proved that this LBL coating could significantly promote and enhance new collagen formation among the graft fibers. On the basis of these results, we conclude that such CS-HA assembly coating could enhance PET graft biocompatibility in vitro and in vivo, and a CS-HA-coated PET graft has considerable potential as a desirable substitute for ligament reconstruction. PMID:23565685

  10. Effect of temperature on the release of intentionally and non-intentionally added substances from polyethylene terephthalate (PET) bottles into water: chemical analysis and potential toxicity.

    PubMed

    Bach, Cristina; Dauchy, Xavier; Severin, Isabelle; Munoz, Jean-François; Etienne, Serge; Chagnon, Marie-Christine

    2013-08-15

    The purpose of this study was to investigate the impact of temperature on the release of PET-bottle constituents into water and to assess the potential health hazard using in vitro bioassays with bacteria and human cell lines. Aldehydes, trace metals and other compounds found in plastic packaging were analysed in PET-bottled water stored at different temperatures: 40, 50, and 60°C. In this study, temperature and the presence of CO2 increased the release of formaldehyde, acetaldehyde and antimony (Sb). In parallel, genotoxicity assays (Ames and micronucleus assays) and transcriptional-reporter gene assays for estrogenic and anti-androgenic activity were performed on bottled water extracts at relevant consumer exposure levels. As expected, and in accordance with the chemical formulations specified for PET bottles, neither phthalates nor UV stabilisers were present in the water extracts. However, 2,4-di-tert-butylphenol, a degradation compound of phenolic antioxidants, was detected. In addition, an intermediary monomer, bis(2-hydroxyethyl)terephthalate, was found but only in PET-bottled waters. None of the compounds are on the positive list of EU Regulation No. 10/2011. However, the PET-bottled water extracts did not induce any cytotoxic, genotoxic or endocrine-disruption activity in the bioassays after exposure. PMID:23561160

  11. Safety assessment of modified terephthalate polymers as used in cosmetics.

    PubMed

    Becker, Lillian C; Bergfeld, Wilma F; Belsito, Donald V; Hill, Ronald A; Klaassen, Curtis D; Liebler, Daniel C; Marks, James G; Shank, Ronald C; Slaga, Thomas J; Snyder, Paul W; Andersen, F Alan

    2014-01-01

    The safety of 6 modified terephthalate polymers as cosmetic ingredients was assessed. These ingredients mostly function as exfoliants, bulking agents, hair fixatives, and viscosity-increasing agents-nonaqueous. Polyethylene terephthalate (PET) is used in leave-on products up to 100% and in rinse-off products up to 2%. The Cosmetic Ingredient Review Expert Panel (Panel) considered that the PET used in cosmetics is chemically equivalent to that used in medical devices. The Panel determined that the Food and Drug Administration's determination of safety of PET in several medical devices, which included human and animal safety data, can be used as the basis for the determination of safety of PET and related polymers used in cosmetics. Use studies of cosmetic eye products that contain PET demonstrated no ocular irritation or dermal sensitization. The Panel concluded that modified terephthalate polymers were safe as cosmetic ingredients in the practices of use and concentration described in this safety assessment. PMID:25297907

  12. Dimethyl terephthalate (DMT)

    Integrated Risk Information System (IRIS)

    Dimethyl terephthalate ( DMT ) ; CASRN 120 - 61 - 6 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for No

  13. 21 CFR 177.1630 - Polyethylene phthalate polymers.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... following prescribed conditions: (a) Polyethylene phthalate films consist of a base sheet of ethylene... as constituents of the base sheet or as constituents of coatings applied to the base sheet. (b) Polyethylene phthalate articles consist of a base polymer of ethylene terephthalate polymer, or...

  14. Synthesis and Verification of Biobased Terephthalic Acid from Furfural

    PubMed Central

    Tachibana, Yuya; Kimura, Saori; Kasuya, Ken-ichi

    2015-01-01

    Exploiting biomass as an alternative to petrochemicals for the production of commodity plastics is vitally important if we are to become a more sustainable society. Here, we report a synthetic route for the production of terephthalic acid (TPA), the monomer of the widely used thermoplastic polymer poly(ethylene terephthalate) (PET), from the biomass-derived starting material furfural. Biobased furfural was oxidised and dehydrated to give maleic anhydride, which was further reacted with biobased furan to give its Diels-Alder (DA) adduct. The dehydration of the DA adduct gave phthalic anhydride, which was converted via phthalic acid and dipotassium phthalate to TPA. The biobased carbon content of the TPA was measured by accelerator mass spectroscopy and the TPA was found to be made of 100% biobased carbon. PMID:25648201

  15. Synthesis and Verification of Biobased Terephthalic Acid from Furfural

    NASA Astrophysics Data System (ADS)

    Tachibana, Yuya; Kimura, Saori; Kasuya, Ken-Ichi

    2015-02-01

    Exploiting biomass as an alternative to petrochemicals for the production of commodity plastics is vitally important if we are to become a more sustainable society. Here, we report a synthetic route for the production of terephthalic acid (TPA), the monomer of the widely used thermoplastic polymer poly(ethylene terephthalate) (PET), from the biomass-derived starting material furfural. Biobased furfural was oxidised and dehydrated to give maleic anhydride, which was further reacted with biobased furan to give its Diels-Alder (DA) adduct. The dehydration of the DA adduct gave phthalic anhydride, which was converted via phthalic acid and dipotassium phthalate to TPA. The biobased carbon content of the TPA was measured by accelerator mass spectroscopy and the TPA was found to be made of 100% biobased carbon.

  16. Synthesis and verification of biobased terephthalic acid from furfural.

    PubMed

    Tachibana, Yuya; Kimura, Saori; Kasuya, Ken-ichi

    2015-01-01

    Exploiting biomass as an alternative to petrochemicals for the production of commodity plastics is vitally important if we are to become a more sustainable society. Here, we report a synthetic route for the production of terephthalic acid (TPA), the monomer of the widely used thermoplastic polymer poly(ethylene terephthalate) (PET), from the biomass-derived starting material furfural. Biobased furfural was oxidised and dehydrated to give maleic anhydride, which was further reacted with biobased furan to give its Diels-Alder (DA) adduct. The dehydration of the DA adduct gave phthalic anhydride, which was converted via phthalic acid and dipotassium phthalate to TPA. The biobased carbon content of the TPA was measured by accelerator mass spectroscopy and the TPA was found to be made of 100% biobased carbon. PMID:25648201

  17. Preparation and dyeing of super hydrophilic polyethylene terephthalate fabric

    NASA Astrophysics Data System (ADS)

    Zheng, D. D.; Zhou, J. F.; Xu, F.; Zhang, F. X.; Zhang, G. X.

    2016-07-01

    In this study, the dyeing properties of PET fabrics modified with sulfuric acid was investigated using disperse red E-4B and disperse blue 2BLNG-L at high temperature and high pressure. The results revealed that the sulfuric acid modification improved the K/S value of dyeing PET fabrics, and the modified PET fabric could be dyed uniformly. The a, b, C, L and H of modified PET fabric were almost the same as that of original PET fabric. The water contact angles were still 0o after 10s, indicating that the hydrophilic property of modified PET fabrics still kept excellent. The wash fastness of dyed PET fabrics after modification was generally good.

  18. 76 FR 8770 - Polyethylene Terephthalate (Pet) Film From Korea

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-15

    ... institution (75 FR 53711, September 1, 2010) were adequate. A record of the Commissioners' votes, the... FR 68036 (November 8, 2002). Even where electronic filing of a document is permitted, certain... Electronic Filing Procedures, 67 FR 68168, 68173 (November 8, 2002). Additional written submissions to...

  19. 76 FR 54791 - Polyethylene Terephthalate (PET) Film From Korea

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-02

    ... Procedure (19 CFR 207.2(f)). Background The Commission instituted this review on September 1, 2010 (75 FR 53711) and determined on February 8, 2011 that it would conduct a full review (76 FR 8770, February 15... 15, 2011 (76 FR 8770). The hearing was held in Washington, DC, on June 28, 2011, and all persons...

  20. 75 FR 53711 - Polyethylene Terephthalate (PET) Film From Korea

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-01

    ... Department of Commerce (Commerce) issued an antidumping duty order on imports of PET film from Korea (56 FR..., Commerce issued a continuation of the antidumping duty order on imports of PET film from Korea (65 FR 11984... issued a continuation of the antidumping duty order on imports of PET film from Korea (70 FR 61118)....

  1. Polyethylene Glycol 3350

    MedlinePlus

    Polyethylene glycol 3350 is used to treat occasional constipation. Polyethylene glycol 3350 is in a class of medications ... Polyethylene glycol 3350 comes as a powder to be mixed with a liquid and taken by mouth. ...

  2. The Role of Benzoate in Anaerobic Degradation of Terephthalate

    PubMed Central

    Kleerebezem, Robbert; Pol, Look W. Hulshoff; Lettinga, Gatze

    1999-01-01

    The effects of acetate, benzoate, and periods without substrate on the anaerobic degradation of terephthalate (1,4-benzene-dicarboxylate) by a syntrophic methanogenic culture were studied. The culture had been enriched on terephthalate and was capable of benzoate degradation without a lag phase. When incubated with a mixture of benzoate and terephthalate, subsequent degradation with preference for benzoate was observed. Both benzoate and acetate inhibited the anaerobic degradation of terephthalate. The observed inhibition is partially irreversible, resulting in a decrease (or even a complete loss) of the terephthalate-degrading activity after complete degradation of benzoate or acetate. Irreversible inhibition was characteristic for terephthalate degradation only because the inhibition of benzoate degradation by acetate could well be described by reversible noncompetitive product inhibition. Terephthalate degradation was furthermore irreversibly inhibited by periods without substrate of only a few hours. The inhibition of terephthalate degradation due to periods without substrate could be overcome through incubation of the culture with a mixture of benzoate and terephthalate. In this case no influence of a period without substrate was observed. Based on these observations it is postulated that decarboxylation of terephthalate, resulting in the formation of benzoate, is strictly dependent on the concomitant fermentation of benzoate. In the presence of higher concentrations of benzoate, however, benzoate is the favored substrate over terephthalate, and the culture loses its ability to degrade terephthalate. In order to overcome the inhibition of terephthalate degradation by benzoate and acetate, a two-stage reactor system is suggested for the treatment of wastewater generated during terephthalic acid production. PMID:10049877

  3. Application of several advanced oxidation processes for the destruction of terephthalic acid (TPA).

    PubMed

    Thiruvenkatachari, Ramesh; Kwon, Tae Ouk; Jun, Jung Chul; Balaji, Subramanian; Matheswaran, Manickam; Moon, Il Shik

    2007-04-01

    Terephthalic acid (TPA) is widely applied as a raw material in making polyester fiber, polyethylene terephthalate (PET) bottles, polyester films, etc. TPA is toxic and is known to act as endocrine disruptor. TPA wastewater is traditionally treated by biological process and this study aims to evaluate the effectiveness of several advanced oxidation processes on TPA removal. The oxidation processes studied were: UV-TiO(2), UV-H(2)O(2), UV-H(2)O(2)-Fe, O(3), O(3)/Fe, O(3)/TiO(2), UV-O(3)-H(2)O(2)-Fe and UV-O(3)-H(2)O(2)-Fe-TiO(2). The results indicate that the time required for the complete destruction of 50 ppm of TPA can be minimized from 10h using UV-TiO(2) system, to less than 10 min by UV-H(2)O(2)-Fe-O(3) system. Some of the likely organic intermediates identified during TPA destruction include, benzoquinone, benzene, maleic acid and oxalic acid. Possible destruction pathway of TPA has been proposed. TPA degradation by various systems was also analyzed based on the reaction kinetics and operating costs. PMID:17023113

  4. Production of Diethyl Terephthalate from Biomass-Derived Muconic Acid.

    PubMed

    Lu, Rui; Lu, Fang; Chen, Jiazhi; Yu, Weiqiang; Huang, Qianqian; Zhang, Junjie; Xu, Jie

    2016-01-01

    We report a cascade synthetic route to directly obtain diethyl terephthalate, a replacement for terephthalic acid, from biomass-derived muconic acid, ethanol, and ethylene. The process involves two steps: First, a substituted cyclohexene system is built through esterification and Diels-Alder reaction; then, a dehydrogenation reaction provides diethyl terephthalate. The key esterification reaction leads to improved solubility and modulates the electronic properties of muconic acid, thus promoting the Diels-Alder reaction with ethylene. With silicotungstic acid as the catalyst, nearly 100% conversion of muconic acid was achieved, and the cycloadducts were formed with more than 99.0% selectivity. The palladium-catalyzed dehydrogenation reaction preferentially occurs under neutral or mildly basic conditions. The total yield of diethyl terephthalate reached 80.6% based on the amount of muconic acid used in the two-step synthetic process. PMID:26592149

  5. Pyrolysis and hydrolysis of mixed polymer waste comprising polyethylene-terephthalate and polyethylene to sequentially recover [monomers

    DOEpatents

    Evans, R.J.; Chum, H.L.

    1998-10-13

    A process is described for using fast pyrolysis in a carrier gas to convert a plastic waste feed stream having a mixed polymeric composition in a manner such that pyrolysis of a given polymer to its high value monomeric constituent occurs prior to pyrolysis of other plastic components therein comprising: selecting a first temperature program range to cause pyrolysis of said given polymer to its high value monomeric constituent prior to a temperature range that causes pyrolysis of other plastic components; selecting a catalyst and support for treating said feed streams with said catalyst to effect acid or base catalyzed reaction pathways to maximize yield or enhance separation of said high value monomeric constituent in said temperature program range; differentially heating said feed stream at a heat rate within the first temperature program range to provide differential pyrolysis for selective recovery of optimum quantities of the high value monomeric constituent prior to pyrolysis of other plastic components; separating the high value monomeric constituents; selecting a second higher temperature range to cause pyrolysis of a different high value monomeric constituent of said plastic waste and differentially heating the feed stream at the higher temperature program range to cause pyrolysis of the different high value monomeric constituent; and separating the different high value monomeric constituent. 83 figs.

  6. Polyethylene Glycol 3350

    MedlinePlus

    Polyethylene glycol 3350 comes as a powder to be mixed with a liquid and taken by mouth. It is usually taken once a day as needed for up to ... to produce a bowel movement.To use the powder, follow these steps: If you are using polyethylene ...

  7. 21 CFR 177.1630 - Polyethylene phthalate polymers.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    .... Acrylonitrile. Methacrylonitrile. Vinyl chloride. Itaconic acid. Styrene-maleic anhydride resin, partial 2... terephthalate or terephthalic acid with ethylene glycol, modified with one or more of the following: Azelaic acid, dimethyl azelate, dimethyl sebacate, sebacic acid. Ethylene terephthalate copolymers: Prepared...

  8. Picosecond UV laser induced scribing of polyethylene terephthalate (PET) films for the enhancement of their flexibility

    NASA Astrophysics Data System (ADS)

    Kang, Min Gi; Kim, Changhwan; Lee, Yong Joong; Kim, Sung Yeol; Lee, Ho

    2016-08-01

    Flexible devices has received a great attention due to their high portability, lightness, and ease of shape reconfiguration. To achieve high flexibility, controlling the mechanical properties of the substrate materials is of importance. In this paper, we controlled the local flexibility of PET films via UV laser scribing. The bending test of the films revealed that their bending curvatures, the associated mechanical damages, and the required bending forces could be successfully tuned by controlling the number and the depth of the scribed lines. Our simple strategy of using laser scribing will find its usefulness in flexible device applications where high flexibility and mechanical stability are required.

  9. Oxygen transport through polyethylene terephthalate (PET) coated with plasma-polymerized acetylene at atmospheric pressure

    NASA Astrophysics Data System (ADS)

    Wemlinger, Erik; Pedrow, Patrick; Garcia-Pérez, Manuel; Sablani, Shyam

    2011-10-01

    Moser et al. have shown that oxygen transport through polyethyleneterephthalate (PET) is reduced by a factor of up to 120 when, at reduced pressure, hydrogenated amorphous carbon film with thickness less than 100 nm is applied to the PET substrate. Our work includes using atmospheric pressure cold plasma to grow a plasma-polymerized acetylene film on PET substrate and measuring reductions in oxygen transport. The reactor utilizes corona discharges and is operated at 60 Hz with a maximum voltage of 10 kV RMS. Corona streamers emanate from an array of needles with an average radius of curvature of 50 μm. The reactor utilizes a cylindrical reaction chamber with a vertical orientation such that argon carrier gas and acetylene precursor gas are introduced at the top then pass through the cold plasma activation zone and then through a grounded stainless steel mesh. Acetylene radicals are incident on the PET substrate and form plasma-polymerized acetylene film. Moser et al. have shown that oxygen transport through polyethyleneterephthalate (PET) is reduced by a factor of up to 120 when, at reduced pressure, hydrogenated amorphous carbon film with thickness less than 100 nm is applied to the PET substrate. Our work includes using atmospheric pressure cold plasma to grow a plasma-polymerized acetylene film on PET substrate and measuring reductions in oxygen transport. The reactor utilizes corona discharges and is operated at 60 Hz with a maximum voltage of 10 kV RMS. Corona streamers emanate from an array of needles with an average radius of curvature of 50 μm. The reactor utilizes a cylindrical reaction chamber with a vertical orientation such that argon carrier gas and acetylene precursor gas are introduced at the top then pass through the cold plasma activation zone and then through a grounded stainless steel mesh. Acetylene radicals are incident on the PET substrate and form plasma-polymerized acetylene film. E.M. Moser, R. Urech, E. Hack, H. Künzli, E. Müller, Thin Solid Films, 317, 1998, pp. 388-392.

  10. 78 FR 78333 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-12-26

    ...: Electronic Filing Procedures; Administrative Protective Order Procedures, 76 FR 39263 (July 6, 2011). The... Review and Final Rescission, in Part, 72 FR 58809 (October 17, 2007), and accompanying Issues and... Antidumping Proceedings: Assessment of Antidumping Duties, 76 FR 65694 (October 24, 2011), for a...

  11. Chitosan coatings onto polyethylene terephthalate for the development of potential active packaging material

    NASA Astrophysics Data System (ADS)

    Zemljič, Lidija Fras; Tkavc, Tina; Vesel, Alenka; Šauperl, Olivera

    2013-01-01

    In this paper advanced surface treatment of PET plastic film is presented for introduction of antimicrobial properties as a potential application for food (as for example meat) packaging material. Adsorption/desorption of chitosan onto PET plastic film surface was studied using several analytical techniques such as: X-Ray Photoelectron Spectroscopy (XPS), ATR-FTIR spectroscopy and titrations. Kinetic desorption of chitosan from PET surface was analysed by polyelectrolyte titration and spectrophotometric Ninhydrine reaction. Standard antimicrobial test ASTM E2149-01 was performed for functionalised PET materials in order to determine their antimicrobial properties; i. e. to measure the reductions of some of the meat pathogens; such as bacteria Salmonella enterica, Campylobacter spp., Escherichia coli, Listeria monocytogenes and fungi Candida albicans.

  12. Factors affecting degradation of polyethylene terephthalate (PET) during pre-flotation conditioning

    SciTech Connect

    Caparanga, Alvin R. Basilia, Blessie A.; Dagbay, Kevin B.; Salvacion, Jonathan W.L.

    2009-09-15

    In general, plastics are exposed to different degrading agents in every procedure involved in their recovery from waste mixture and from subsequent recycling. In this study, two methods of pre-flotation conditioning were used to determine how these methods affect the general properties of the pre-conditioned PET particles to be recovered from the PET-PVC mixture. The first method comprised the conditioning of PET samples using an alkaline solution of nonionic surfactant (Triton X-100) based on the patent by the Goodyear Tire and Rubber Company. The second method, developed in this study, was a conditioning process which used an alkali-less solution of the same nonionic surfactant (Triton X-100) used in the first method. The following analytical methods were used to characterize properties of the pre-conditioned PET samples that were correlated to relative degradation of the samples: differential scanning calorimetry (DSC), for thermal behavior of the samples; FT-IR spectroscopy, for functional groups present in the samples; and, Pohl's method, for carboxyl end-group concentration count. Results show that in addition to water the presence of NaOH in the conditioning solution contributes to the further degradation of the polymer.

  13. Chemometric tools to highlight non-intentionally added substances (NIAS) in polyethylene terephthalate (PET).

    PubMed

    Kassouf, Amine; Maalouly, Jacqueline; Chebib, Hanna; Rutledge, Douglas N; Ducruet, Violette

    2013-10-15

    In an effort to identify non-intentionally added substances (NIAS), which is still a challenging task for analytical chemists, PET pellets, preforms and bottles were analyzed by an optimized headspace solid phase microextraction coupled to gas chromatography-mass spectrometry (HS-SPME/GC-MS). Fingerprints obtained by the proposed method were analyzed by three chemometric tools: Principal Components Analysis (PCA), Independent Components Analysis (ICA) and a multi-block method (Common Components and Specific Weights Analysis CCSWA) in order to extract pertinent variations in NIAS concentrations. Total ion current (TIC) chromatograms were used for PCA and ICA while extracted ion chromatograms (EIC) were used for CCSWA, each ion corresponding to a block. PCA managed to discriminate pellets and preforms from bottles due to several NIAS. Volatiles like 2-methyl-1,3-dioxolane, ethylene glycol, ethylbenzene and xylene were responsible for the discrimination of pellets and preforms. Less volatile compounds like linear aldehydes and phthalates were responsible for the discrimination of bottles. ICA showed more specific discriminations especially for bottles and pellets while CCSWA managed to discriminate preforms. The proposed methodology, combining HS-SPME/GC-MS with chemometric tools proved its efficiency in highlighting NIAS in PET samples in a relatively simple and fast approach compared to classical techniques. PMID:24054684

  14. 76 FR 47540 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-05

    ... Antidumping Proceedings: Affiliated Party Sales in the Ordinary Course of Trade, 67 FR 69186, 69187 (November... Determination of Sales at Less Than Fair Value: Static Random Access Memory Semiconductors From Taiwan, 63 FR..., Sheet, and Strip (PET Film) From Taiwan, 67 FR 44174 (July 1, 2002), as corrected in 67 FR 46566...

  15. 75 FR 81570 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-28

    ... FR 44175 (July 1, 2002). On December 24, 2009, the Department received a timely request from SRF, in..., 75 FR 10758 (March 9, 2010) (NSR Initiation).\\1\\ \\1\\ As stated in the initiation notice, due to the... by one week, to March 8, 2010. See NSR Initiation, 75 FR at 10758. On April 6, 2010, the...

  16. 75 FR 40784 - Polyethylene Terephthalate Film, Sheet, and Strip from the Republic of Korea: Preliminary Results...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-07-14

    ... economic planning, sales promotion, order processing, and technical assistance), the level of performance..., Finding, or Suspended Investigation; Opportunity to Request Administrative Review, 74 FR 26202 (June 1... Administrative Reviews and Deferral of Administrative Review, 74 FR 37690 (July 29, 2009). On August 6, 2009,...

  17. 77 FR 46687 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-08-06

    ..., Sheet, and Strip from India, 67 FR 44175 (July 1, 2002). \\2\\ See Antidumping or Countervailing Duty Order, Finding, or Suspended Investigation; Opportunity To Request Administrative Review, 76 FR 38609... Reviews and Requests for Revocation in Part, 76 FR 53404 (August 26, 2011). \\5\\ See...

  18. 76 FR 76365 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates: Preliminary...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-07

    ... Sales at Less Than Fair Value for the United Arab Emirates, 73 FR 66595 (November 10, 2008) (Order). On...; Opportunity to Request Administrative Review, 75 FR 67079 (November 1, 2010). In response, on November 29..., 75 FR 81565, 81570 (December 28, 2010). On January 27, 2011, the Department issued an...

  19. 76 FR 27005 - Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea: Initiation and...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-10

    ...., Industrial Phosphoric Acid from Israel: Final Results of Antidumping Duty Changed Circumstances Review, 59 FR... Korea, 56 FR 25669 (June 5, 1991). On September 26, 1997, the Department published the notice of final... Determination of Antidumping Duty Investigation, 62 FR 50557 (September 26, 1997) (Antidumping...

  20. 75 FR 69629 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Extension...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-11-15

    ... FR 68229 (December 23, 2009). On August 16, 2010, the Department published the preliminary results of...: Preliminary Results and Preliminary Rescission, in Part, of Antidumping Duty Administrative Review, 75...

  1. 77 FR 1668 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-01-11

    ... FR 38609, 38610 (July 1, 2011). The Department received a timely request from Petitioners \\1\\ for a... Requests for Revocation in Part, 76 FR 53404 (August 26, 2011). On August 23, 2011, Vacmet and Polypacks... FR 58248 (September 20, 2011). On November 25, 2011, Petitioners withdrew their request for...

  2. 77 FR 9892 - Polyethylene Terephthalate Film, Sheet and Strip from India: Preliminary Intent to Rescind...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-02-21

    ...; Opportunity To Request Administrative Review, 76 FR 38609, 38610 (July 1, 2011). The Department received a... Countervailing Duty Administrative Reviews and Requests for Revocation in Part, 76 FR 53404 (August 26, 2011... Part, of Countervailing Duty Administrative Review, 76 FR 58248 (September 20, 2011). On September...

  3. 76 FR 72676 - Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-25

    ..., 76 FR 48122 (August 8, 2011) (Preliminary Results). This administrative review covers one respondent... rebuttal briefs within five days after the due date for filing case briefs. See Preliminary Results, 76 FR..., Sheet, and Strip from Brazil, 73 FR 55035, 55036 (September 24, 2008). These deposit requirements,...

  4. 76 FR 61085 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Extension...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-10-03

    ... Revocation in Part, 75 FR 81565 (December 28, 2010). On July 18, 2011, the Department extended the time... Antidumping Duty Administrative Review, 76 FR 42113 (July 18, 2011). The preliminary results of this review... the Tariff Act of 1930, as Amended, 70 FR 24533 (May 10, 2005). The Department will extend...

  5. 77 FR 3730 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in Part, of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-01-25

    ... Order, Finding, or Suspended Investigation; Opportunity To Request Administrative Review, 76 FR 38609... Revocation in Part, 76 FR 53404 (August 26, 2011). On August 23, 2011, Vacmet and Polypacks withdrew their... Strip From India: Rescission, In Part, of Antidumping Duty Administrative Review, 76 FR 58244...

  6. 77 FR 14501 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-12

    ... Requests for Revocation in Part, 76 FR 53404 (August 26, 2011). The Department initiated the review with... Strip From India: Rescission, In Part, of Antidumping Duty Administrative Review, 76 FR 58244 (September... and Strip From India: Rescission, In Part, of Antidumping Duty Administrative Review, 77 FR...

  7. 76 FR 30908 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-27

    ...: Preliminary Results of Antidumping Duty New Shipper Review, 75 FR 81570 (December 28, 2010) (Preliminary..., 75 FR at 81573. See Memorandum To Interested Parties From Elfi Blum, International Trade Compliance... Results of Antidumping Duty New Shipper Review, 76 FR 12937 (March 9, 2011). On April 13, 2011,...

  8. 77 FR 73428 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-10

    ... Administrative Review and Final Rescission, in Part, 72 FR 58809 (October 17, 2007), and accompanying Issues and... Assessment Rate in Certain Antidumping Proceedings: Final Modification, 77 FR 8101 (February 14, 2012). We... Proceedings: Assessment of Antidumping Duties, 76 FR 65694 (October 24, 2011). The final results of...

  9. 76 FR 71512 - Polyethylene Terephthalate Film, Sheet, and Strip From Korea: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-18

    ... Administrative Review, 76 FR 40325 (July 8, 2011) (Preliminary Results). The respondent subject to this review is... Duty Order, 76 FR 57715 (September 16, 2011) (Revocation Notice); see also ``Termination of Suspension... and Deferral of Administrative Reviews, 76 FR 45227 (July 28, 2011). \\5\\ Because Kolon is the...

  10. 77 FR 19634 - Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission of Countervailing Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-04-02

    ... Administrative Review, 76 FR 38609, 38610 (July 1, 2011). The Department received a timely request from... Reviews and Requests for Revocation in Part, 76 FR 53404 (August 26, 2011) (Initiation Notice). Prior to... From India: Rescission, In Part, of Countervailing Duty Administrative Review, 76 FR 58248...

  11. 78 FR 35245 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-06-12

    ...-2011, 77 FR 73428 (December 10, 2012), and accompanying Decision Memorandum (``Preliminary Results..., Green Packing, DuPont Group, and Wanhua et al.\\6\\ \\2\\ See id., 77 FR at 73429. \\3\\ In the Preliminary... Emirates, 73 FR 66595 (November 10, 2008). Changes Since the Preliminary Results Based on the...

  12. 78 FR 9670 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results of Administrative...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-11

    ... Strip From India: Preliminary Results of Antidumping Duty Administrative Review, 77 FR 46687 (August 6... Preliminary Results, see Preliminary Results, 77 FR at 46692. Weighted- average Manufacturer/ exporter dumping... Certain Antidumping Duty Proceedings; Final Modification, 77 FR 8101 (February 14, 1012)...

  13. 76 FR 30910 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results of Countervailing...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-27

    ... Shipper Review, 75 FR 81574 (December 28, 2010) (Preliminary Results), the following events have occurred... accordance with 19 CFR 351.309(c) and the Preliminary Results, 75 FR at 81583. See Memorandum To Interested... From India: Extension of Time Limit for Final Results of Countervailing Duty New Shipper Review, 76...

  14. 78 FR 48143 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-07

    ... Results of New Shipper Review and Partial Rescission of Administrative Review, 73 FR 8273 (February 13... Antidumping Duty Administrative Review and New Shipper Review, 73 FR 49162 (August 20, 2008). In this review... Polyplex is the non- selected respondent. The Department preliminarily determines that SRF did, and...

  15. 77 FR 73010 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates; Preliminary...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-07

    ...: Final Modification, 77 FR 8101 (February 14, 2012). The final results of this review shall be the basis... and Amended Final Determination of Sales at Less Than Fair Value for the United Arab Emirates, 73 FR... determines that sales of subject merchandise have been made below normal value by JBF and that FLEX did...

  16. 76 FR 47546 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-05

    ... Strip from India, 67 FR 44175 (July 1, 2002) (PET Film India Order). On July 1, 2010, the Department... FR 38074 (July 1, 2010). In response, on July 27, 2010, and August 2, 2010, Ester and SRF Limited... Deferral of Initiation of Administrative Review, 75 FR 53274, 53276 (August 31, 2010). The...

  17. 76 FR 76943 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-09

    ..., 76 FR 47546 (August 5, 2011) (Preliminary Results). DATES: Effective Date: December 9, 2011. FOR...: Ester Industries Ltd. (Ester). Based on the results of our analysis of the comments received, we did not make any changes to the preliminary results. However, the Department did make changes to...

  18. Spray coating of carbon nanotube on polyethylene terephthalate film for touch panel application.

    PubMed

    Park, Chul; Kim, Seok Won; Lee, Yun-Su; Lee, Sung Ho; Song, Kyu Ho; Park, Lee Soon

    2012-07-01

    From a technical perspective, the major limiting factors for the wide adoption of CNT films are the DC conductivity, uniformity of sheet resistance and good adhesion of CNT on film substrate. In this study, the effects of sonificator and process time on the zeta potential and sheet resistance of the CNT-PET film show that although the dispersing power of horn-type sonificator is stronger than that of bath-type, the SWCNT solution obtained with horn-type sonificator agglomerates faster. Likewise, it has been noted that the SWCNT solutions with low enough zeta potentials exhibit higher sheet resistance after making CNT-PET films due to the damage to SWCNTs caused by high dispersion force. Since the spray coating of SWCNT solution gives the SWCNT-SDS composite layer on PET film after drying, the excess SDS should be washed off. The removal of excess SDS was conducted by dipping in the 3 N HNO3 and SOCl2 solution and washing with deionized water followed by heat treatment in a 120 degrees C convection oven for 30 min. The lift-off of SWCNT-SDS composite layer after 40 min dipping in the 3 N HNO3 solution appeared to be due to the continued permeation leading to swelling of the SDS layer by the 3 N HNO3 aqueous solution. It was found that ten times of spray coating cycle gave CNT-PET film the sheet resistance of 310 Ω/[square] and transmittance of 81%. The TSP made with CNT-PET film exhibited a performance equal to the one made with ITO-PET film. PMID:22966570

  19. 78 FR 9668 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-11

    ... Antidumping Duty Administrative Review, 77 FR 46704 (August 6, 2012) (Preliminary Results). DATES: Effective... Antidumping Duty Proceedings; Final Modification, 77 FR 8101 (February 14, 2012) (Final Modification for... Duties, 68 FR 23954 (May 6, 2003). Cash Deposit Requirements The following deposit requirements will...

  20. 77 FR 31833 - Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Notice of Rescission of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-05-30

    ..., 76 FR 82268 (December 30, 2011). This review covers Terphane, Inc. and Terphane, Ltda. Petitioners... Polyester Film, Inc., SKC, Inc., and Toray Plastics (America), Inc. (collectively, petitioners),...

  1. 76 FR 9745 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-22

    ...: Preliminary Results of Antidumping Duty Administrative Review, 75 FR 49902 (August 16, 2010) (Preliminary... Duty Administrative Review, 75 FR 76954 (December 10, 2010). On December 22, 2010, the Department... Proceedings: Assessment of Antidumping Duties, 68 FR 23954 (May 6, 2003). This clarification will apply...

  2. 78 FR 50029 - Polyethylene Terephthalate Film, Sheet and Strip From Brazil: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-16

    ... Revoke the Order (in Part); 2011-2012, 78 FR 15686 (March 12, 2013) and the accompanying Decision... Countervailing Duty Proceedings: Assessment of Antidumping Duties, 68 FR 23954 (May 6, 2003). We intend to issue..., Inc., SKC, Inc., and Toray Plastics (America), Inc. (collectively, Petitioners), the Department...

  3. 78 FR 48651 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan; Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-09

    ... of the Antidumping Duty Administrative Review, 77 FR 76456 (December 28, 2012). DATES: Effective Date... Assessment Rate in Certain Antidumping Proceedings: Final Modification, 77 FR 8101 (February 14, 2012). The... and Countervailing Duty Proceedings: Assessment of Antidumping Duties, 68 FR 23954 (May 6, 2003)....

  4. Thermal properties of Poly(ethylene terephthalate) recovered from municipal solid waste by steam autoclaving

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The goal of this study was to evaluate the effects of steam autoclaving on the properties of PET, data which could ultimately be applied to determine the most likely end use of this potentially huge waste stream. Through the course of the study it was determined that stretch blow molding in bottle ...

  5. Chemical recycling of poly(ethylene terephthalate) (PET) by hydrolysis and glycolysis.

    PubMed

    Carta, Daniela; Cao, Giacomo; D'Angeli, Claudio

    2003-01-01

    In this paper we review an interesting method of PET recycling, i.e. chemical recycling; it is based on the concept of depolymerizing the condensation polymer through solvolytic chain cleavage into low molecular products which can be purified and reused as raw materials for the production of high-quality chemical products. In this work our attention is confined to the hydrolysis (neutral, acid and alkaline) and glycolysis processes of PET chemical recycling; operating conditions and mechanism of each method are reported and described. The neutral hydrolysis has an auto accelerating character; two kinetic models have been proposed: an half-order and a second order kinetic model. The acid hydrolysis could be explained by a modified shrinking core model under chemical reaction control and the alkaline hydrolysis by a first-order model with respect to hydroxide ion concentration. To describe glycolysis, two different kinetic models have been proposed where EG can act or not as internal catalyst. Further experimental and theoretical investigations are required to shed light on the promising processes of PET chemical recycling reviewed in this work. PMID:14699998

  6. Migration of antimony from polyethylene terephthalate used in mineral water bottles.

    PubMed

    Carneado, S; Hernández-Nataren, E; López-Sánchez, J F; Sahuquillo, A

    2015-01-01

    The influence of storage time and temperature on Sb migration from PET bottles into mineral water was studied in short-term tests lasting up to 15 days and long-term studies lasting up to 220 days. Samples purchased were stored in three different coloured bottles: clear (CL), light blue (LB) and dark blue (DB). Sb migration was assayed by HG-AFS for total determination and HPLC-ICP-MS for speciation analysis. Migration studies showed that waters stored at 4 and 20 °C were not subject to Sb migration. At 40 °C there was a significant increase in Sb concentration, although the maximum limit established by the European Union (5.0 μgL(-)(1)) was not exceeded, whereas at 60 °C samples were subject to considerable Sb migration after 30 days of storage. In this case, the maximum limit established by the European Union was exceeded and both Sb (V) and Sb (III) were detected. PMID:25053092

  7. Factors affecting degradation of polyethylene terephthalate (PET) during pre-flotation conditioning.

    PubMed

    Caparanga, Alvin R; Basilia, Blessie A; Dagbay, Kevin B; Salvacion, Jonathan W L

    2009-09-01

    In general, plastics are exposed to different degrading agents in every procedure involved in their recovery from waste mixture and from subsequent recycling. In this study, two methods of pre-flotation conditioning were used to determine how these methods affect the general properties of the pre-conditioned PET particles to be recovered from the PET-PVC mixture. The first method comprised the conditioning of PET samples using an alkaline solution of nonionic surfactant (Triton X-100) based on the patent by the Goodyear Tire and Rubber Company. The second method, developed in this study, was a conditioning process which used an alkali-less solution of the same nonionic surfactant (Triton X-100) used in the first method. The following analytical methods were used to characterize properties of the pre-conditioned PET samples that were correlated to relative degradation of the samples: differential scanning calorimetry (DSC), for thermal behavior of the samples; FT-IR spectroscopy, for functional groups present in the samples; and, Pohl's method, for carboxyl end-group concentration count. Results show that in addition to water the presence of NaOH in the conditioning solution contributes to the further degradation of the polymer. PMID:19394808

  8. Laser transmission welding of Clearweld-coated polyethylene glycol terephthalate by incremental scanning technique

    NASA Astrophysics Data System (ADS)

    Wang, Y. Y.; Wang, A. H.; Weng, Z. K.; Xia, H. B.

    2016-06-01

    Transmission laser welding using Incremental Scanning Technique(TWIST) mode and conventional contour welding mode were adopted to investigate laser transmission welding of 0.5 mm thick PET plate. A 1064 nm fiber laser was used to weld PET at the (TWIST) mode, and an 808 nm diode laser was applied to conduct the conventional contour welding. The Clearweld coating was used as laser absorbing material. The influences of laser parameters (i.e. defocusing distance, distance between two circles) on the quality of weld seams were analyzed by optical microscopy. Moreover, geometry and shear strength of the weld zone were tested to optimize laser parameters. Additionally, the water vapor permeability (WVP) of weld seams was measured to test hermetical capacity. Results show that the shear strength and hermetic capacity of weld seam by TWIST mode are at the same level in comparison with that of the conventional contour welding.

  9. 75 FR 69400 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-11-12

    ... Duty New Shipper Reviews, 75 FR 10758 (March 9, 2010). This new shipper review covers one producer and... Preliminary Results of Countervailing Duty New Shipper Review, 75 FR 52717 (August 27, 2010). The Department... issues pertaining to the bona fides of this new shipper. In addition, we need further information...

  10. 75 FR 65450 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-10-25

    ... India: Initiation of Antidumping Duty and Countervailing Duty New Shipper Reviews, 75 FR 10758 (March 9... Limit for Preliminary Results of Antidumping Duty New Shipper Review, 75 FR 52717 (August 27, 2010). The... the bona fides of the new shipper, including the examination of importer and customer information....

  11. 75 FR 80457 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-22

    ... bona fides of the new shipper and SRF Limited's reported sales data. See First Extension, 75 FR at... Duty New Shipper Reviews, 75 FR 10758 (March 9, 2010). This new shipper review covers one producer and... Antidumping Duty New Shipper Review, 75 FR 52717 (August 27, 2010) (First Extension). On October 18, 2010,...

  12. 75 FR 52717 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-27

    ... Duty New Shipper Reviews, 75 FR 10758 (March 9, 2010). This new shipper review covers one producer and..., As Amended, 70 FR 24533 (May 10, 2005). Extension of Time Limit for the Preliminary Results Section... SRF's supplemental questionnaire response in its examination of the bona fides of SRF's...

  13. 75 FR 79336 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-20

    ... Shipper Reviews, 75 FR 10758 (March 9, 2010). This new shipper review covers one producer and exporter of... Preliminary Results of Countervailing Duty New Shipper Review, 75 FR 52717 (August 27, 2010). On November 12...: Extension of Time Limit for Preliminary Results of Countervailing Duty New Shipper Review, 75 FR...

  14. 77 FR 14493 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-12

    ... Administrative Review, 76 FR 68140 (November 3, 2011) (``Preliminary Results''). DATES: Effective Date: March 12... the People's Republic of China: Final Determination of Sales at Less Than Fair Value, 73 FR 55039... margin calculations for Tianjin Wanhua Co., Ltd. (``Wanhua'') and Sichuan Dongfang Insulating Material...

  15. 76 FR 68140 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-03

    ... Than Fair Value for the United Arab Emirates, 73 FR 66595 (November 10, 2008) (``Orders''). \\2\\ See... Administrative Review, 75 FR 67079 (November 1, 2010). \\3\\ See Initiation of Antidumping and Countervailing Duty Administrative Reviews and Requests for Revocation in Part, 75 FR 81565 (December 28, 2010) (``Initiation...

  16. 75 FR 49893 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-16

    ...''), Shanghai Xishu Electric Material Co., Ltd. (``Xishu''), and Shanghai Uchem Co., Ltd. (``Uchem'').\\1\\ The... Emirates, 73 FR 66595 (November 10, 2008) (``Orders''). \\2\\ See Initiation of Antidumping and Countervailing Duty Administrative Reviews and Request for Revocation in Part, 74 FR 68229 (December 23,...

  17. 77 FR 46704 - Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary Results of Antidumping...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-08-06

    ... Film) from Taiwan, 67 FR 44174 (July 1, 2002), as corrected in 67 FR 46566 (July 15, 2002). \\2\\ See... Administrative Review, 76 FR 38609, 38610 (July 1, 2011). \\3\\ Petitioners are DuPont Teijin Films, Mitsubishi... Administrative Determination Deadlines Pursuant to the Tariff Act of 1930, As Amended,70 FR 24533 (May 10,...

  18. 78 FR 60311 - Polyethylene Terephthalate Film, Sheet, and Strip From Brazil, China, and the United Arab...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-10-01

    ..., China, and the United Arab Emirates (73 FR 66595). The Commission is conducting reviews to determine... employees, and Commission rule 201.15(b) (19 CFR 201.15(b)), 73 FR 24609 (May 5, 2008). This advice was... machinery in place and ready to operate), normal operating levels (hours per week/weeks per year), time...

  19. 75 FR 78968 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates: Preliminary...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-17

    ... Quality ] Steel Products from Brazil, 70 FR 48668, 48670 (August 19, 2005), unchanged in Notice of Final... Quality Steel Products from Brazil, 70 FR 62297 (October 31, 2005). The Department found that pursuant to... during the same shorter averaging periods. See Stainless Steel Plate in Coils From Belgium: Final...

  20. 76 FR 9753 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-22

    ... polyester chips and master batch chips by using the simple-average of the two weighted average surrogate...'') classification 3907.60.20 to value Bright Polyester Chip and Master Batch Chip. Issue 4: Whether the Department..., of Antidumping Duty Administrative Review, 75 FR 49893 (August 16, 2010) (``Preliminary...

  1. 75 FR 6634 - Polyethylene Terephthalate Film, Sheet, and Strip from India: Final Results of Countervailing...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-02-10

    ... Countervailing Duty Administrative Review, 74 FR 39631 (August 7, 2009) (Preliminary Results). Based on the... EPCGS licenses treated as contingent liability loans, we will deducted the relevant application...

  2. Biodegradable poly(terephthalate-co-phosphate)s: synthesis, characterization and drug-release properties

    PubMed Central

    Mao, Hai-Quan; Shipanova-Kadiyala, Irina; Zhao, Zhong; Dang, Wenbin; Brown, Angela; Leong, Kam W.

    2008-01-01

    To develop biodegradable polymers with favorable physicochemical and biological properties, we have synthesized a series of poly(terephthalate-co-phosphate)s using a two-step polycondensation. The diol 1,4-bis(2-hydroxyethyl) terephthalate was first reacted with ethylphosphorodichloridate (EOP), and then chain-extended with terephthaloyl chloride (TC). Incorporation of phosphate into the poly(ethylene terephthalate) backbone rendered the co-polymers soluble in chloroform and biodegradable, lowered the Tg, decreased the crystallinity and increased the hydrophilicity. With an EOP/TC molar feed ratio of 80 : 20, the polymer exhibited good film-forming property, yielding at 86.6 ± 1.6% elongation with an elastic modulus of 13.76 ± 2.66 MPa. This polymer showed a favorable toxicity profile in vitro and good tissue biocompatibility in the muscular tissue of mice. In vitro the polymer lost 21% of mass in 21 days, but only 20% for up to 4 months in vivo. It showed no deterioration of properties after sterilization by γ -irradiation at 2.5 Mrad on solid CO2. Release of FITC-BSA from the microspheres was diffusion-controlled and exceeded 80% completion in two days. Release of the hydrophobic cyclosporine-A from microspheres was however much more sustained and near zero-ordered, discharging 60% in 70 days. A limited structure–property relationship has been established for this co-polymer series. The co-polymers became more hydrolytically labile as the phosphate component (EOP) was increased and the side chains were switched from the ethoxy to the methoxy structure. Converting the methoxy group to a sodium salt further increased the degradation rate significantly. The chain rigidity as reflected in the Tg values of the co-polymers decreased according to the following diol structure in the backbone: ethylene glycol > 2-methylpropylene diol > 2,2-dimethylpropylene diol. The wide range of physicochemical properties obtainable from this co-polymer series should help the

  3. 40 CFR 721.10352 - Dimethyl terephthalate, polymer with alkyl diol and substituted benzoates (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Dimethyl terephthalate, polymer with... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10352 Dimethyl terephthalate, polymer... subject to reporting. (1) The chemical substance identified generically as dimethyl terephthalate,...

  4. 40 CFR 721.10352 - Dimethyl terephthalate, polymer with alkyl diol and substituted benzoates (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Dimethyl terephthalate, polymer with... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10352 Dimethyl terephthalate, polymer... subject to reporting. (1) The chemical substance identified generically as dimethyl terephthalate,...

  5. 40 CFR 721.10352 - Dimethyl terephthalate, polymer with alkyl diol and substituted benzoates (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Dimethyl terephthalate, polymer with... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10352 Dimethyl terephthalate, polymer... subject to reporting. (1) The chemical substance identified generically as dimethyl terephthalate,...

  6. Synthesis of terephthalic acid via Diels-Alder reactions with ethylene and oxidized variants of 5-hydroxymethylfurfural

    PubMed Central

    Pacheco, Joshua J.; Davis, Mark E.

    2014-01-01

    Terephthalic acid (PTA), a monomer in the synthesis of polyethylene terephthalate (PET), is obtained by the oxidation of petroleum-derived p-xylene. There is significant interest in the synthesis of renewable, biomass-derived PTA. Here, routes to PTA starting from oxidized products of 5-hydroxymethylfurfural (HMF) that can be produced from biomass are reported. These routes involve Diels-Alder reactions with ethylene and avoid the hydrogenation of HMF to 2,5-dimethylfuran. Oxidized derivatives of HMF are reacted with ethylene over solid Lewis acid catalysts that do not contain strong Brønsted acids to synthesize intermediates of PTA and its equally important diester, dimethyl terephthalate (DMT). The partially oxidized HMF, 5-(hydroxymethyl)furoic acid (HMFA), is reacted with high pressure ethylene over a pure-silica molecular sieve containing framework tin (Sn-Beta) to produce the Diels-Alder dehydration product, 4-(hydroxymethyl)benzoic acid (HMBA), with 31% selectivity at 61% HMFA conversion after 6 h at 190 °C. If HMFA is protected with methanol to form methyl 5-(methoxymethyl)furan-2-carboxylate (MMFC), MMFC can react with ethylene in the presence of Sn-Beta for 2 h to produce methyl 4-(methoxymethyl)benzenecarboxylate (MMBC) with 46% selectivity at 28% MMFC conversion or in the presence of a pure-silica molecular sieve containing framework zirconium (Zr-Beta) for 6 h to produce MMBC with 81% selectivity at 26% MMFC conversion. HMBA and MMBC can then be oxidized to produce PTA and DMT, respectively. When Lewis acid containing mesoporous silica (MCM-41) and amorphous silica, or Brønsted acid containing zeolites (Al-Beta), are used as catalysts, a significant decrease in selectivity/yield of the Diels-Alder dehydration product is observed. PMID:24912153

  7. Synthesis of terephthalic acid via Diels-Alder reactions with ethylene and oxidized variants of 5-hydroxymethylfurfural.

    PubMed

    Pacheco, Joshua J; Davis, Mark E

    2014-06-10

    Terephthalic acid (PTA), a monomer in the synthesis of polyethylene terephthalate (PET), is obtained by the oxidation of petroleum-derived p-xylene. There is significant interest in the synthesis of renewable, biomass-derived PTA. Here, routes to PTA starting from oxidized products of 5-hydroxymethylfurfural (HMF) that can be produced from biomass are reported. These routes involve Diels-Alder reactions with ethylene and avoid the hydrogenation of HMF to 2,5-dimethylfuran. Oxidized derivatives of HMF are reacted with ethylene over solid Lewis acid catalysts that do not contain strong Brønsted acids to synthesize intermediates of PTA and its equally important diester, dimethyl terephthalate (DMT). The partially oxidized HMF, 5-(hydroxymethyl)furoic acid (HMFA), is reacted with high pressure ethylene over a pure-silica molecular sieve containing framework tin (Sn-Beta) to produce the Diels-Alder dehydration product, 4-(hydroxymethyl)benzoic acid (HMBA), with 31% selectivity at 61% HMFA conversion after 6 h at 190 °C. If HMFA is protected with methanol to form methyl 5-(methoxymethyl)furan-2-carboxylate (MMFC), MMFC can react with ethylene in the presence of Sn-Beta for 2 h to produce methyl 4-(methoxymethyl)benzenecarboxylate (MMBC) with 46% selectivity at 28% MMFC conversion or in the presence of a pure-silica molecular sieve containing framework zirconium (Zr-Beta) for 6 h to produce MMBC with 81% selectivity at 26% MMFC conversion. HMBA and MMBC can then be oxidized to produce PTA and DMT, respectively. When Lewis acid containing mesoporous silica (MCM-41) and amorphous silica, or Brønsted acid containing zeolites (Al-Beta), are used as catalysts, a significant decrease in selectivity/yield of the Diels-Alder dehydration product is observed. PMID:24912153

  8. Simultaneous recovery of benzene-rich oil and metals by steam pyrolysis of metal-poly(ethylene terephthalate) composite waste.

    PubMed

    Kumagai, Shogo; Grause, Guido; Kameda, Tomohito; Yoshioka, Toshiaki

    2014-03-18

    The possibility of simultaneous recovery of benzene and metals from the hydrolysis of poly(ethylene terephthalate) (PET)-based materials such as X-ray films, magnetic tape, and prepaid cards under a steam atmosphere at a temperature of 450 °C was evaluated. The hydrolysis resulted in metal-containing carbonaceous residue and volatile terephthalic acid (TPA). The effects of metals and additives on the recovery process were also investigated. All metals were quantitatively recovered, and silver, maghemite (γ-Fe2O3), and anatase (TiO2) were recovered without any changes in their crystal structures or compositions. In a second step, TPA was decarboxylized in the presence of calcium oxide (CaO) at 700 °C, producing benzene with an average yield of 34% and purity of 76%. Maghemite (γ-Fe2O3) incorporated in magnetic tape and prepaid cards could decarboxylate TPA. Aluminum present in the prepaid cards produced hydrogen by the reaction with steam. However, the presence of metals had no adverse influence on the recovery of benzene-rich oil in the presence of CaO. Therefore, this method can be applied to PET-based materials containing inorganic substances, which cannot be recycled effectively otherwise. PMID:24527803

  9. 120 MeV Ni Ion beam induced modifications in poly (ethylene terephthalate) used in commercial bottled water

    SciTech Connect

    Kumar, Vijay; Sonkawade, R. G.; Ali, Yasir; Dhaliwal, A. S.

    2012-06-05

    We report the effects of heavy ion irradiation on the optical, structural, and chemical properties of polyethylene terephthalate (PET) film used in commercial bottled water. PET bottles were exposed with 120 MeV Ni ions at fluences varying from 3 x 10{sup 10} to 3 x 10{sup 12} ion/cm{sup 2}. The modifications so induced were analyzed by using UV-Vis, X-ray diffraction (XRD) and Fourier Transform Infrared (FTIR) spectroscopy. Substantial decrease in optical band gap is observed with the increase in ion fluence. In the FTIR spectra, most of bands are decreased due the degradation of the molecular structure. XRD measurements show the decrease in peak intensity, which reflects the loss of crystallinity after irradiation.

  10. 120 MeV Ni Ion beam induced modifications in poly (ethylene terephthalate) used in commercial bottled water

    NASA Astrophysics Data System (ADS)

    Kumar, Vijay; Sonkawade, R. G.; Ali, Yasir; Dhaliwal, A. S.

    2012-06-01

    We report the effects of heavy ion irradiation on the optical, structural, and chemical properties of polyethylene terephthalate (PET) film used in commercial bottled water. PET bottles were exposed with 120 MeV Ni ions at fluences varying from 3 × 1010 to 3 × 1012 ion/cm2. The modifications so induced were analyzed by using UV-Vis, X-ray diffraction (XRD) and Fourier Transform Infrared (FTIR) spectroscopy. Substantial decrease in optical band gap is observed with the increase in ion fluence. In the FTIR spectra, most of bands are decreased due the degradation of the molecular structure. XRD measurements show the decrease in peak intensity, which reflects the loss of crystallinity after irradiation.

  11. Modeling cutinase enzyme regulation in polyethylene terepthalate plastic biodegradation

    NASA Astrophysics Data System (ADS)

    Apri, M.; Silmi, M.; Heryanto, T. E.; Moeis, M. R.

    2016-04-01

    PET (Polyethylene terephthalate) is a plastic material that is commonly used in our daily life. The high production of PET and others plastics that can be up to three hundred million tons per year, is not matched by its degradation rate and hence leads to environmental pollution. To overcome this problem, we develop a biodegradation system. This system utilizes LC Cutinase enzyme produced by engineered escherichia coli bacteria to degrade PET. To make the system works efficaciously, it is important to understand the mechanism underlying its enzyme regulation. Therefore, we construct a mathematical model to describe the regulation of LC Cutinase production. The stability of the model is analyzed. We show that the designated biodegradation system can give an oscillatory behavior that is very important to control the amount of inclusion body (the miss-folded proteins that reduce the efficiency of the biodegradation system).

  12. 21 CFR 177.1660 - Poly (tetramethylene terephthalate).

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Poly (tetramethylene terephthalate). 177.1660 Section 177.1660 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated...

  13. 21 CFR 177.1660 - Poly (tetramethylene terephthalate).

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1660 Poly (tetramethylene terephthalate). Poly(tetramethylene... part. (c) Specifications. (1) Inherent viscosity of a 0.50 percent solution of the polymer in...

  14. Method for casting polyethylene pipe

    NASA Technical Reports Server (NTRS)

    Elam, R. M., Jr.

    1973-01-01

    Short lengths of 7-cm ID polyethylene pipe are cast in a mold which has a core made of room-temperature-vulcanizable (RTV) silicone. Core expands during casting and shrinks on cooling to allow for contraction of the polyethylene.

  15. Method for shaping polyethylene tubing

    NASA Technical Reports Server (NTRS)

    Kramer, R. C.

    1981-01-01

    Method forms polyethylene plastic tubing into configurations previously only possible with metal tubing. By using polyethylene in place of copper or stain less steel tubing inlow pressure systems, fabrication costs are significantly reduced. Polyethylene tubing can be used whenever low pressure tubing is needed in oil operations, aircraft and space applications, powerplants, and testing laboratories.

  16. Polyethylene Glycol Propionaldehydes

    NASA Technical Reports Server (NTRS)

    Harris, Joe M.; Sedaghat-Herati, Mohammad R.; Karr, Laurel J.

    1992-01-01

    New class of compounds derived from polyethylene glycol (PEG's) namely, PEG-propionaldehydes, offers two important advantages over other classes of PEG aldehyde derivatives: compounds exhibit selective chemical reactivity toward amino groups and are stable in aqueous environment. PEG's and derivatives used to couple variety of other molecules, such as, to tether protein molecules to surfaces. Biotechnical and biomedical applications include partitioning of two phases in aqueous media; immobilization of such proteins as enzymes, antibodies, and antigens; modification of drugs; and preparation of protein-rejecting surfaces. In addition, surfaces coated with PEG's and derivatives used to control wetting and electroosmosis. Another potential application, coupling to aminated surfaces.

  17. Disintegration of porous polyethylene prostheses.

    PubMed

    Kerr, A G; Riley, D N

    1999-06-01

    A Plastipore (porous polyethylene) Total Ossicular Replacement Prosthesis gave an excellent initial hearing result which was maintained for 14 years. Hearing then began to deteriorate and revision surgery showed disintegration of the prosthesis and a defect in the stapes footplate. Histological examination confirmed previous findings in porous polyethylene with multinucleated foreign body giant cells and breakdown of the material. PMID:10384839

  18. A novel hierarchically structured and highly hydrophilic poly(vinyl alcohol-co-ethylene)/poly(ethylene terephthalate) nanoporous membrane for lithium-ion battery separator

    NASA Astrophysics Data System (ADS)

    Xia, Ming; Liu, Qiongzhen; Zhou, Zhou; Tao, Yifei; Li, MuFang; Liu, Ke; Wu, Zhihong; Wang, Dong

    2014-11-01

    A novel hierarchically structured and highly hydrophilic poly(vinyl alcohol-co-ethylene)/poly(ethylene terephthalate) nanoporous separator (referred to NFs/PET/NFs) composed of a poly(ethylene terephthalate) (PET) nonwoven sandwiched between two interconnected poly(vinyl alcohol-co-ethylene) (PVA-co-PE) nanofibrous membranes is successfully developed for lithium-ion battery. Systematical investigations including structural characterization, porosity measurement, water contact angle testing, electrolyte uptake, and thermal shrinkage testing demonstrate that the notable feature of this NFs/PET/NFs nanofibrous separator is an electrolyte-philic, highly porous and hierarchically nanoscaled structure, thus resulting in superior electrolyte wettability, lower thermal shrinkage, and higher ion conductivity, in comparison to the commercial Polypropylene (PP) separator. These structural characteristics enable the NFs/PET/NFs separator to offer an excellent cell performance including outstanding C-rate capability, high capacity and excellent cycling performance. This suggests that the NFs/PET/NFs separator is a promising material for practical application in lithium-ion battery due to it low cost production and high performance.

  19. Interaction between polyethylene films and bromhexine HCl in solid dosage form. V. Effect of packaging materials on the sorption of bromhexine HCl.

    PubMed

    Kukita, T; Furuuchi, S; Nemoto, M; Yoshida, T

    1992-11-01

    A prevention method of the sorption of bromhexine HCl to plastic materials used in packaging was investigated. Four kinds of plastic packaging materials were used: Polyethylene (PE), polyethylene terephthalate (PET), polypropylene (PP) and polyacrylonitrile (PAN). Three polyethylenes having different densities were used. No effect of PE density on the sorption of bromhexine HCl from granules was observed. The effects of different kinds of plastics on the sorption of bromhexine HCl from solution and granules were studied. The sorption of bromhexine HCl to PAN, which had a high relative dielectric constant, was the most depressed among the four plastics. The sorption of meclizine HCl to PAN from the solution was also lowest, the same as bromhexine HCl. PMID:1477930

  20. Preparation of hydroxylated polyethylene surfaces.

    PubMed

    Zand, A; Walter, N; Bahu, M; Ketterer, S; Sanders, M; Sikorski, Y; Cunningham, R; Beholz, L

    2008-01-01

    The surfaces of high-density or ultra-high-molecular-weight polyethylenes were hydroxylated using a two-step process. The wetting and wear properties of the untreated (virgin) and surface hydroxylated polyethylenes were compared. The introduction of hydroxyl groups provided an increase in surface hydrophilicity resulting in reduced wear. Hydrophilicity was analyzed by optical analysis of water contact angle. Wear was determined by weight loss under conditions of a reciprocating pin-on-plate apparatus with the panels immersed in water or calf serum. These results suggest that hydroxylation of polyethylene friction-bearing orthopedic surfaces may lead to a longer joint life. PMID:18318959

  1. Identification of di-2-ethylhexyl terephthalate (DEHTP) metabolites using human liver microsomes for biomonitoring applications.

    PubMed

    Silva, Manori J; Samandar, Ella; Calafat, Antonia M; Ye, Xiaoyun

    2015-06-01

    Di-2-ethylhexyl terephthalate (DEHTP), a structural isomer of the plasticizer di-2-ethylhexyl phthalate (DEHP), is used in food packaging and medical devices, among other applications, and is a potential replacement for DEHP and other ortho-phthalate plasticizers. Identifying sensitive and specific biomarkers of DEHTP is necessary to assess humans' background exposure to DEHTP. Using mass spectrometry, we investigated the metabolism of DEHTP by human liver microsomes to identify in vitro DEHTP metabolites. We unequivocally identified terephthalic acid (TPA) and mono-2-ethylhydroxyhexyl terephthalate (MEHHTP), using authentic standards, and tentatively identified mono-2-ethylhexyl terephthalate (MEHTP) and two other oxidative metabolites of DEHTP: mono-2-ethyloxohexyl terephthalate (MEOHTP), and mono-2-ethyl-5-carboxypentyl terephthalate (MECPTP) from their mass spectrometry fragmentation patterns. We also evaluated the formation of in vitro metabolites of DEHP. DEHTP and DEHP produced similar metabolites, but their metabolite profiles differed considerably. DEHTP metabolized to form TPA, a metabolite of several terephthalates, as the major in vitro metabolite, followed by MEHTP, MEHHTP, MEOHTP and MECPTP. MEHTP, MEHHTP, MEOHTP and MECPTP, which are specific metabolites of DEHTP, may be suitable biomarkers for assessing exposure to DEHTP. Nonetheless, data on the urinary excretion fraction and temporal stability of these metabolites, among other considerations, are needed to demonstrate their utility as exposure biomarkers. PMID:25687528

  2. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph... prescribed conditions: (a) Fluorinated polyethylene food-contact articles are produced by modifying...

  3. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620... Contact Surfaces § 177.1620 Polyethylene, oxidized. Oxidized polyethylene identified in paragraph (a) of... following prescribed conditions: (a) Oxidized polyethylene is the basic resin produced by the mild...

  4. Effect of SiO2-acryl nanohybrid coating layers on transparent conducting oxide-poly(ethylene terephthalate) superstrate.

    PubMed

    Kang, Y T; Kang, D P; Kang, D J; Chung, I D

    2013-05-01

    SiO2-acryl nanohybrid coating layers were produced by hybridizing acrylic resin and surface-modified colloidal silica (CS) nanoparticles. First, CS nanoparticles were modified with methyltrimethoxysilane (MTMS) and vinyltrimethoxysilane (VTMS) by a sol-gel process. The surface-modified CS nanoparticles were then solvent-exchanged to be homogeneous in acrylic resin. The Hybrid materials were mixed in variation with the amount of surface-modified CS nanoparticles, coated with poly(ethylene terephthalate) (PET), then finally cured by UV light to obtain a hybrid coating layer. Field emission scanning electron microscopy (FE-SEM), particle size analysis (using a Zetasizer), and atomic force microscopy (AFM) were performed to determine the morphology of the hybrid thin-films. Thermogravimetric analysis (TGA) was used to investigate the thermal properties. Fourier-transform infrared (FTIR), ultraviolet-visible (UVNis) spectroscopies, and pencil hardness were used to obtain the details of chemical structures, optical properties, and hardness, respectively. The hybrid thin films had shown to be enhanced properties compared to their urethane acrylate prepolymer (UAP) coating film. PMID:23858925

  5. Transient Current Behaviour of Poly (p-hydroxybenzoic acid-co-ethylene terephthalate) Liquid Crystal Polymers

    NASA Astrophysics Data System (ADS)

    Yarramaneni, Sridharbabu; Sharma, Anu; Quamara, J. K.

    2011-07-01

    Transient current behaviour of pristine Poly (p-hydroxybenzoic acid-co-ethylene terephthalate) Liquid crystal polymer which is a copolymer of poly ethylene terephthalate and poly p-hydroxybenzoic acid referred as PET/x.PHB polymer liquid crystals have been studied at different biasing electric fields ranging from 13 kV/cm to 104.3 kV/cm and at temperatures 120° C and 250° C for molar ratio x =0.8.

  6. Electromagnetic Characteristics of Thin Polyethylene-Carbon-Polyethylene Films

    NASA Astrophysics Data System (ADS)

    Volynets, N. I.; Lyubimov, A. G.; Plyushch, A. O.; Poddubskaya, O. G.; Kuzhir, P. P.; Korovin, E. Yu.; Suslyaev, V. I.; Macutkevic, J.; Pikutskaya, E. S.; Baturkin, S. A.; Klochkov, A. Ya.

    2015-09-01

    A method of manufacturing a polyethylene - expanded carbon - polyethylene layered structures which allows thin (down to 90 μm) and flexible sandwiches to be easily made, is suggested. The electromagnetic properties of the manufactured composite materials at frequencies from 1 MHz to 3 GHz, 26-37.5 GHz, and 0.1-1.4 THz are analyzed. It is established that the material so obtained is opaque for the Ka microwave band due to high reflectivity (96-97%), does not transmit electromagnetic radiation of the terahertz range, has a high conductivity (up to 1 S/m) in the frequency range from 1 MHz to 1 GHz, and retains the main physical polyethylene properties (light weight, elasticity, and flexibility).

  7. 76 FR 1135 - Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea: Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-07

    ..., 75 FR 53664 (September 1, 2010) (Notice of Initiation). The Department received a notice of intent to...; Notice of Final Court Decision and Amended Final Determination of Antidumping Duty Investigation, 62 FR... expedited (120-day) sunset review pursuant to 19 CFR 351.218(e)(1)(ii)(C)(2). As a result of this...

  8. Nano-scale temperature dependent visco-elastic properties of polyethylene terephthalate (PET) using atomic force microscope (AFM).

    PubMed

    Grant, Colin A; Alfouzan, Abdulrahman; Gough, Tim; Twigg, Peter C; Coates, Phil D

    2013-01-01

    Visco-elastic behaviour at the nano-level of a commonly used polymer (PET) is characterised using atomic force microscopy (AFM) at a range of temperatures. The modulus, indentation creep and relaxation time of the PET film (thickness=100 μm) is highly sensitive to temperature over an experimental temperature range of 22-175°C. The analysis showed a 40-fold increase in the amount of indentation creep on raising the temperature from 22°C to 100°C, with the most rapid rise occurring above the glass-to-rubber transition temperature (T(g)=77.1°C). At higher temperatures, close to the crystallisation temperature (T(c)=134.7°C), the indentation creep reduced to levels similar to those at temperatures below T(g). The calculated relaxation time showed a similar temperature dependence, rising from 0.6s below T(g) to 1.2s between T(g) and T(c) and falling back to 0.6s above T(c). Whereas, the recorded modulus of the thick polymer film decreases above T(g), subsequently increasing near T(c). These visco-elastic parameters are obtained via mechanical modelling of the creep curves and are correlated to the thermal phase changes that occur in PET, as revealed by differential scanning calorimetry (DSC). PMID:22750040

  9. 76 FR 22867 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates: Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-25

    ... FR 78968 (December 17, 2010) (Preliminary Results). A sales verification of JBF was conducted from... Antidumping Duties, 68 FR 23954 (May 6, 2003). This clarification will apply to entries of subject merchandise... from the United Arab Emirates: Final Determination of Sales at Less Than Fair Value, 73 FR...

  10. 78 FR 19524 - Polyethylene Terephthalate Film, Sheet, and Strip From India and Taiwan; Institution of Five-Year...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-04-01

    ... Department of Commerce issued a countervailing duty order on imports of PET film from India (67 FR 44179) and antidumping duty orders on imports of PET film from India (67 FR 44175) and Taiwan (67 FR 44174). Following... continuation of the countervailing duty order on imports of PET film from India (73 FR 26080) and...

  11. 78 FR 29700 - Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab Emirates: Final Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-05-21

    ... Arab Emirates: Preliminary Results of Antidumping Duty Administrative Review; 2010-2011, 77 FR 73010... Assessment Rate in Certain Antidumping Proceedings: Final Modification, 77 FR 8101 (February 14, 2012). For... Countervailing Duty Proceedings: Assessment of Antidumping Duties, 68 FR 23954 (May 6, 2003). \\7\\ See id.;...

  12. DNA purification using dynamic solid-phase extraction on a rotationally-driven polyethylene-terephthalate microdevice.

    PubMed

    Jackson, K R; Borba, J C; Meija, M; Mills, D L; Haverstick, D M; Olson, K E; Aranda, R; Garner, G T; Carrilho, E; Landers, J P

    2016-09-21

    We report the development of a disposable polyester toner centrifugal device for semi-automated, dynamic solid phase DNA extraction (dSPE) from whole blood samples. The integration of a novel adhesive and hydrophobic valving with a simple and low cost microfabrication method allowed for sequential addition of reagents without the need for external equipment for fluid flow control. The spin-dSPE method yielded an average extraction efficiency of ∼45% from 0.6 μL of whole blood. The device performed single sample extractions or accommodate up to four samples for simultaneous DNA extraction, with PCR-readiness DNA confirmed by effective amplification of a β-globin gene. The purity of the DNA was challenged by a multiplex amplification with 16 targeted amplification sites. Successful multiplexed amplification could routinely be obtained using the purified DNA collected post an on-chip extraction, with the results comparable to those obtained with commercial DNA extraction methods. This proof-of-principle work represents a significant step towards a fully-automated low cost DNA extraction device. PMID:27590539

  13. 76 FR 12937 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-09

    ... Film, Sheet and Strip from India: Preliminary Results of Antidumping Duty New Shipper Review, 75 FR... Preliminary Results concerning the bona fides of the new ] shipper sale. Due to this issue, the Department...

  14. 76 FR 12938 - Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for Final...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-09

    ..., 75 FR 81574 (December 28, 2010) (Preliminary Results). The final results of review are currently due... Preliminary Results concerning the bona fides of the new shipper's sale. Due to this issue, the Department...

  15. 78 FR 9363 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Notice of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-08

    ... People's Republic of China: Final Results of the First Antidumping Duty Administrative Review, 76 FR 9753... Determination Deadlines Pursuant to the Tariff Act of 1930, as Amended, 70 FR 24533 (May 10, 2005). FOR FURTHER... of Production: Labor, 76 FR 36092 (June 21, 2011) (``Labor Methodologies''). Finally, the...

  16. 78 FR 52500 - Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic of China: Notice of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-23

    ... People's Republic of China: Final Results of the First Antidumping Duty Administrative Review, 76 FR 9753... Final Results of Administrative Review Pursuant to Court Decision, 78 FR 9363 (February 8, 2013). \\4... Than Fair Value, 73 FR 55039, 55041 (September 24, 2008). Timken Notice In its decision in Timken,...

  17. Chemical compounds and toxicological assessments of drinking water stored in polyethylene terephthalate (PET) bottles: A source of controversy reviewed.

    PubMed

    Bach, Cristina; Dauchy, Xavier; Chagnon, Marie-Christine; Etienne, Serge

    2012-03-01

    A declaration of conformity according to European regulation No. 10/2011 is required to ensure the safety of plastic materials in contact with foodstuffs. This regulation established a positive list of substances that are authorized for use in plastic materials. Some compounds are subject to restrictions and/or specifications according to their toxicological data. Despite this, the analysis of PET reveals some non-intentionally added substances (NIAS) produced by authorized initial reactants and additives. Genotoxic and estrogenic activities in PET-bottled water have been reported. Chemical mixtures in bottled water have been suggested as the source of these toxicological effects. Furthermore, sample preparation techniques, such as solid-phase extraction (SPE), to extract estrogen-like compounds in bottled water are controversial. It has been suggested that inappropriate extraction methods and sample treatment may result in false-negative or positive responses when testing water extracts in bioassays. There is therefore a need to combine chemical analysis with bioassays to carry out hazard assessments. Formaldehyde, acetaldehyde and antimony are clearly related to migration from PET into water. However, several studies have shown other theoretically unexpected substances in bottled water. The origin of these compounds has not been clearly established (PET container, cap-sealing resins, background contamination, water processing steps, NIAS, recycled PET, etc.). Here, we surveyed toxicological studies on PET-bottled water and chemical compounds that may be present therein. Our literature review shows that contradictory results for PET-bottled water have been reported, and differences can be explained by the wide variety of analytical methods, bioassays and exposure conditions employed. PMID:22196043

  18. Temperature-modulated calorimetry of the frequency dependence of the glass transition of poly(ethylene terephthalate) and ....

    SciTech Connect

    Wunderlich, B.; Okazaki, I.

    1997-03-01

    Temperature-modulated differential scanning calorimetry, TMDSC, is new technique that permits to measure the apparent heat capacity vs modulation frequency. The method is briefly described and a quasi- isothermal measurement method is used to derive the kinetic parameters for PET and PS. A first-order kinetics expression was used to describe the approach to equilibrium and point out the limits caused by asymmetry and cooperativity of the kinetics. Use of a complex description of heat capacity and entropy is discussed. Activation energies vary from 75 to 350 kJ/mol, dependent on thermal pretreatment and the preexponential factor is correlated with the activation energy.

  19. 76 FR 13128 - Polyethylene Terephthalate Film, Sheet, and Strip (PET Film) From Taiwan: Extension of Time Limit...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-10

    ... Duty Administrative Reviews and Deferral of Initiation of Administrative Review, 75 FR 53274 (August 31... Determination Deadlines Pursuant to the Tariff Act of 1930, As Amended, 70 FR 24533 (May 10, 2005). Accordingly...: March 10, 2011. FOR FURTHER INFORMATION CONTACT: Emily Halle or Gene Calvert, AD/CVD Operations,...

  20. Degradable polyethylene: fantasy or reality.

    PubMed

    Roy, Prasun K; Hakkarainen, Minna; Varma, Indra K; Albertsson, Ann-Christine

    2011-05-15

    Plastic waste disposal is one of the serious environmental issues being tackled by our society today. Polyethylene, particularly in packaging films, has received criticism as it tends to accumulate over a period of time, leaving behind an undesirable visual footprint. Degradable polyethylene, which would enter the eco-cycle harmlessly through biodegradation would be a desirable solution to this problem. However, the "degradable polyethylene" which is presently being promoted as an environmentally friendly alternative to the nondegradable counterpart, does not seem to meet this criterion. This article reviews the state of the art on the aspect of degradability of polyethylene containing pro-oxidants, and more importantly the effect these polymers could have on the environment in the long run. On exposure to heat, light, and oxygen, these polymers disintegrate into small fragments, thereby reducing or increasing the visual presence. However, these fragments can remain in the environment for prolonged time periods. This article also outlines important questions, particularly in terms of time scale of complete degradation, environmental fate of the polymer residues, and possible accumulation of toxins, the answers to which need to be established prior to accepting these polymers as environmentally benign alternatives to their nondegradable equivalents. It appears from the existing literature that our search for biodegradable polyethylene has not yet been realized. PMID:21495645

  1. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... chlorination of polyethylene conforming to the density, maximum n-hexane extractable fraction, and maximum... polyethylene is limited to use only as a modifier admixed at levels not exceeding 15 weight percent in...

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

    PubMed

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

    2015-10-01

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

  3. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  4. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  5. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  6. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620... Components of Single and Repeated Use Food Contact Surfaces § 177.1620 Polyethylene, oxidized. Oxidized polyethylene identified in paragraph (a) of this section may be safely used as a component of...

  7. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Polyethylene. 573.780 Section 573.780 Food and... Listing § 573.780 Polyethylene. (a) Identity. Polyethylene consists of basic polymers manufactured by the catalytic polymerization of ethylene. (b) Specifications. (1) For the purposes of this section,...

  8. 21 CFR 177.1615 - Polyethylene, fluorinated.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene, fluorinated. 177.1615 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1615 Polyethylene, fluorinated. Fluorinated polyethylene, identified in paragraph (a) of this section, may be safely used as food-contact articles...

  9. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620... Components of Single and Repeated Use Food Contact Surfaces § 177.1620 Polyethylene, oxidized. Oxidized polyethylene identified in paragraph (a) of this section may be safely used as a component of...

  10. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Polyethylene. 573.780 Section 573.780 Food and... Listing § 573.780 Polyethylene. (a) Identity. Polyethylene consists of basic polymers manufactured by the catalytic polymerization of ethylene. (b) Specifications. (1) For the purposes of this section,...

  11. Chemical and toxicological evaluation of pyrotechnically disseminated terephthalic acid smoke.

    PubMed

    Muse, W T; Anthony, J S; Bergmann, J D; Burnett, D C; Crouse, C L; Gaviola, B P; Thomson, S A

    1997-11-01

    The terephthalic acid (TPA) smoke obscurants (M-83 grenade and M-8 smoke pot) were developed by the U.S. Army for training purposes to replace the more toxic hexachloroethane (HC) smoke. Inhalation toxicity testing and chemical characterization of pyrotechnically generated TPA was conducted to assess the health hazard potential of TPA and its combustion products. Fisher 344 rats were subjected to acute and repeated exposures to TPA smoke generated from the M-83 grenade. Acute exposure levels ranged from 150-1,900 mg/m3 for 30 minutes and repeated dose exposures ranged from 128-1,965 mg/m3 for 30 min/day for 5 days. Exposed and control rats were evaluated for toxic signs, and histopathologic changes. During exposure, the rats exhibited slight to moderate lacrimation, rhinorrhea, lethargy and dyspnea, which reversed within 1-hr post-exposure. No deaths occurred, even at the highest smoke concentrations. Histopathological changes were confined to exposure related nasal necrosis and inflammation in both the acute and repeated dose exposures at levels above 900 mg/m3. Chemical characterization of the M-83 grenade and the M-8 smoke pot showed that formaldehyde, benzene and carbon monoxide were the major organic vapor by-products formed. These by-products were above their respective ACGIH threshold limit values at various concentrations, but should not pose a hazard if the smoke is deployed in an open area. Overall, TPA is a safer training smoke to replace the HC smoke. PMID:9433658

  12. Community and Proteomic Analysis of Methanogenic Consortia Degrading Terephthalate

    PubMed Central

    Wu, Feng-Yau; Chuang, Hui-Ping; Chen, Wei-Yu; Huang, Hung-Jen; Chen, Shu-Hui; Liu, Wen-Tso

    2013-01-01

    Degradation of terephthalate (TA) through microbial syntrophy under moderately thermophilic (46 to 50°C) methanogenic conditions was characterized by using a metagenomic approach (A. Lykidis et al., ISME J. 5:122–130, 2011). To further study the activities of key microorganisms responsible for the TA degradation, community analysis and shotgun proteomics were used. The results of hierarchical oligonucleotide primer extension analysis of PCR-amplified 16S rRNA genes indicated that Pelotomaculum, Methanosaeta, and Methanolinea were predominant in the TA-degrading biofilms. Metaproteomic analysis identified a total of 482 proteins and revealed a distinctive distribution pattern of microbial functions expressed in situ. The results confirmed that TA was degraded by Pelotomaculum spp. via the proposed decarboxylation and benzoyl-coenzyme A-dependent pathway. The intermediate by-products, including acetate, H2/CO2, and butyrate, were produced to support the growth of methanogens, as well as other microbial populations that could further degrade butyrate. Proteins related to energy production and conservation, and signal transduction mechanisms (that is, chemotaxis, PAS/GGDEF regulators, and stress proteins) were highly expressed, and these mechanisms were important for growth in energy-limited syntrophic ecosystems. PMID:23064332

  13. Multiple Syntrophic Interactions in a Terephthalate-Degrading Methanogenic Consortium

    SciTech Connect

    Lykidis, Athanasios; Chen, Chia-Lung; Tringe, Susannah G.; McHardy, Alice C.; Copeland, Alex 5; Kyrpides, Nikos C.; Hugenholtz, Philip; Liu, Wen-Tso

    2010-08-05

    Terephthalate (TA) is one of the top 50 chemicals produced worldwide. Its production results in a TA-containing wastewater that is treated by anaerobic processes through a poorly understood methanogenic syntrophy. Using metagenomics, we characterized the methanogenic consortium tinside a hyper-mesophilic (i.e., between mesophilic and thermophilic), TA-degrading bioreactor. We identified genes belonging to dominant Pelotomaculum species presumably involved in TA degradation through decarboxylation, dearomatization, and modified ?-oxidation to H{sub 2}/CO{sub 2} and acetate. These intermediates are converted to CH{sub 4}/CO{sub 2} by three novel hyper-mesophilic methanogens. Additional secondary syntrophic interactions were predicted in Thermotogae, Syntrophus and candidate phyla OP5 and WWE1 populations. The OP5 encodes genes capable of anaerobic autotrophic butyrate production and Thermotogae, Syntrophus and WWE1 have the genetic potential to oxidize butyrate to COsub 2}/H{sub 2} and acetate. These observations suggest that the TA-degrading consortium consists of additional syntrophic interactions beyond the standard H{sub 2}-producing syntroph ? methanogen partnership that may serve to improve community stability.

  14. Exposure to the polyester PET precursor—terephthalic acid induces and perpetuates DNA damage-harboring non-malignant human breast cells

    PubMed Central

    Luciani-Torres, Maria Gloria; Moore, Dan H.; Dairkee, Shanaz H.

    2015-01-01

    Identification of early perturbations induced in cells from non-cancerous breast tissue is critical for understanding possible breast cancer risk from chemical exposure. We have demonstrated previously that exposure to the ubiquitous xenoestrogens, bisphenol A (BPA) and methyl paraben, promotes the hallmarks of cancer in non-malignant human high-risk donor breast epithelial cells (HRBECs) isolated from several donors. Here we show that terephthalic acid (TPA), a major chemical precursor of polyethylene terephthalate (PET) containers used for the storage of food and beverages, increased the ERα: ERβ ratio in multiple HRBEC samples, suggesting an estrogenic effect. Although, like BPA and methyl paraben, TPA also promoted resistance to tamoxifen-induced apoptosis, unlike these chemicals instead of inducing an increased S-phase fraction, TPA treatment arrested cell proliferation. DNA-PK, ATM and members of the MRN complex, known to be involved in DNA damage sensor and effector proteins, were elevated indicating induction of DNA strand breaks. Early DNA damage checkpoint response, mediated through p53/p21, led to G1 arrest in TPA-exposed cells. Removal of TPA from the growth medium resulted in the rapid induction of BCL2, increasing the ratio of anti-: pro-apoptotic proteins, together with overexpression of Cyclin A/CDK2 proteins. Consequently, despite elevated p53pSer15 and H2AXpSer139, indicating sustained DNA damage, TPA exposed cells resumed robust growth rates seen prior to TPA exposure. The propensity for the perpetuation of DNA aberrations that activate DNA damage pathways in non-malignant breast cells justifies careful consideration of human exposure to TPA, particularly at vulnerable life stages. PMID:25411358

  15. Single electron states in polyethylene

    SciTech Connect

    Wang, Y.; MacKernan, D.; Cubero, D. E-mail: n.quirke@imperial.ac.uk; Coker, D. F.; Quirke, N. E-mail: n.quirke@imperial.ac.uk

    2014-04-21

    We report computer simulations of an excess electron in various structural motifs of polyethylene at room temperature, including lamellar and interfacial regions between amorphous and lamellae, as well as nanometre-sized voids. Electronic properties such as density of states, mobility edges, and mobilities are computed on the different phases using a block Lanczos algorithm. Our results suggest that the electronic density of states for a heterogeneous material can be approximated by summing the single phase density of states weighted by their corresponding volume fractions. Additionally, a quantitative connection between the localized states of the excess electron and the local atomic structure is presented.

  16. Single electron states in polyethylene

    NASA Astrophysics Data System (ADS)

    Wang, Y.; MacKernan, D.; Cubero, D.; Coker, D. F.; Quirke, N.

    2014-04-01

    We report computer simulations of an excess electron in various structural motifs of polyethylene at room temperature, including lamellar and interfacial regions between amorphous and lamellae, as well as nanometre-sized voids. Electronic properties such as density of states, mobility edges, and mobilities are computed on the different phases using a block Lanczos algorithm. Our results suggest that the electronic density of states for a heterogeneous material can be approximated by summing the single phase density of states weighted by their corresponding volume fractions. Additionally, a quantitative connection between the localized states of the excess electron and the local atomic structure is presented.

  17. Poly(ethylene oxide) functionalization

    DOEpatents

    Pratt, Russell Clayton

    2014-04-08

    A simple procedure is provided by which the hydroxyl termini of poly(ethylene oxide) can be appended with functional groups to a useful extent by reaction and precipitation. The polymer is dissolved in warmed toluene, treated with an excess of organic base and somewhat less of an excess of a reactive acylating reagent, reacted for several hours, then precipitated in isopropanol so that the product can be isolated as a solid, and salt byproducts are washed away. This procedure enables functionalization of the polymer while not requiring laborious purification steps such as solvent-solvent extraction or dialysis to remove undesirable side products.

  18. 21 CFR 177.1345 - Ethylene/1,3-phenylene oxyethylene isophthalate/ terephthalate copolymer.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ethylene/1,3-phenylene oxyethylene isophthalate/ terephthalate copolymer. 177.1345 Section 177.1345 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as...

  19. 21 CFR 177.1660 - Poly (tetra-methyl-ene tere-phtha-late).

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Poly (tetra-methyl-ene tere-phtha-late). 177.1660 Section 177.1660 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and...

  20. 1,4-Diazo­niabicyclo­[2.2.2]octane terephthalate

    PubMed Central

    Yang, E; Song, Xu-Chun; Zhu, Jian-Wei

    2008-01-01

    In the title compound, C6H14N2+·C8H4O4 2−, the protonated 1,4-diazo­niabicyclo­[2.2.2]octane cations and the deprotonated terephthalate anions are alternately linked by N—H⋯O hydrogen bonds into chains. PMID:21201746

  1. 21 CFR 177.1660 - Poly (tetra-methylene tereph-thalate).

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Poly (tetra-methylene tereph-thalate). 177.1660 Section 177.1660 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated...

  2. A solvent induced crystallisation method to imbue bioactive ingredients of neem oil into the compact structure of poly (ethylene terephthalate) polyester.

    PubMed

    Ali, Wazed; Sultana, Parveen; Joshi, Mangala; Rajendran, Subbiyan

    2016-07-01

    Neem oil, a natural antibacterial agent from neem tree (Azadarichtaindica) has been used to impart antibacterial activity to polyester fabrics. Solvent induced polymer modification method was used and that facilitated the easy entry of neem molecules into the compact structure of polyethylene terephthalate (PET) polyester. The polyester fabric was treated with trichloroacetic acid-methylene chloride (TCAMC) solvent system at room temperature prior to treatment with neem oil. The concentration of TCAMC and the treatment time were optimised. XRD and SEM results showed that the TCAMC treatment causes polymer modification and morphological changes in the PET polyester. Antibacterial activity of TCAMC pre-treated and neem-oil-treated polyester fabric was tested using AATCC qualitative and quantitative methods. Both Gram-positive and Gram-negative organisms were used to determine the antimicrobial activity. It was observed that the treated fabric registers substantial antimicrobial activity against both the Staphylococcus aureus (Gram-positive) and the Escherichia coli (Gram-negative) and the effect increases with the increase in concentration of TCAMC treatment. The antibacterial effect remains substantial even after 25 launderings. A kinetic growth study involving the effect of antibacterial activity at various incubation times was carried out. PMID:27127070

  3. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Polyethylene. 573.780 Section 573.780 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food Additive Listing § 573.780 Polyethylene. (a)...

  4. 21 CFR 177.1240 - 1,4-Cyclohexylene dimethylene terephthalate and 1,4-cyclohexylene dimethylene isophthalate...

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... condensation of dimethyl terephthalate and dimethyl isophthalate with 1,4-cyclohexanedimethanol, to which may...) The copolymer, when extracted with distilled water at reflux temperature for 2 hours, yields...

  5. Porous heterometallic Cd(II)-Ca(II)-terephthalate: Synthesis, structure, luminescent and gas adsorption properties

    NASA Astrophysics Data System (ADS)

    Liu, Haiping; Dong, Yanli; Ren, Hailiang

    2016-03-01

    A new heterometallic poly(dihydrate-one and a half terephthalate-cadmium calcium) coordination polymer, namely [CdCa(pdc)1.5(H2O)2]n (1, H2pdc = terephthalic acid), has been successfully obtained by the solvothermal reactions of H2pdc, Cd(NO3)2·4H2O and Ca(NO3)2·4H2O. Single crystal X-ray diffraction analysis reveals that compound 1 features a 3D porous framework based on 1D chain subunits. Moreover, compound 1 is luminescent and exhibits high adsorption capacities for H2, CH4 and CO2 at room temperature.

  6. Crystallization studies of polyethylene -poly(ethylene glycol) graft copolymers

    NASA Astrophysics Data System (ADS)

    Mark, P. R.; Hovey, G. E.; Murthy, N. S.; Breitenkamp, K.; Kade, M.; Emerick, T.

    2006-03-01

    Structure and crystallization behavior of three copolymers obtained by grafting poly (ethylene glycol) (PEG) chains to polyethylene (PE) main chain was investigated by variable temperature x-ray diffraction and thermal analysis. The results show that PEG side chains and PE main chains crystallize into separate domains. This is especially true when grafted chains are long (50 and 100 repeat units), in which the PEG domains are same as in PEG homopolymer both in structure and in melting behavior. In the copolymer with shorter chains (25 repeat units), the PEG crystals are not distinct and melting is broad. The PEG domains can be dissolved in water or ethanol without altering the mechanical integrity of the film. PE crystallites in both samples are similar to that in PE homopolymer. For instance, the thermal expansion of the basal cell plane (a- and b-axes) of the PE domains agrees well with that of PE homopolymer over the entire temperature range from ambient to melt. However, the chain-axis dimension PE-lattice in the copolymer is shorter by ˜ 0.05 å and the basal dimensions are larger by ˜ 0.05 å. The changes in these dimensions due to the changes in the length of the grafted PEG chains were investigated.

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

    PubMed Central

    Perz, Veronika; Bleymaier, Klaus; Sinkel, Carsten; Kueper, Ulf; Bonnekessel, Melanie; Ribitsch, Doris; Guebitz, Georg M.

    2016-01-01

    The aliphatic-aromatic copolyester poly(butylene adipate-co-butylene terephthalate) (PBAT), also known as ecoflex, contains adipic acid, 1,4-butanediol and terephthalic acid and is proven to be compostable [1], [2], [3]). We describe here data for the synthesis and analysis of poly(butylene adipate-co-butylene terephthalate variants with different adipic acid:terephatalic acid ratios and 6 oligomeric PBAT model substrates. Data for the synthesis of the following oligomeric model substrates are described: mono(4-hydroxybutyl) terephthalate (BTa), bis(4-(hexanoyloxy)butyl) terephthalate (HaBTaBHa), bis(4-(decanoyloxy)butyl) terephthalate (DaBTaBDa), bis(4-(tetradecanoyloxy)butyl) terephthalate (TdaBTaBTda), bis(4-hydroxyhexyl) terephthalate (HTaH) and bis(4-(benzoyloxy)butyl) terephthalate (BaBTaBBa). Polymeric PBAT variants were synthesized with adipic acid:terephatalic acid ratios of 100:0, 90:10, 80:20, 70:30, 60:40 and 50:50. These polymeric and oligomeric substances were used as ecoflex model substrates in enzymatic hydrolysis experiments in the article “Substrate specificities of cutinases on aliphatic-aromatic polyesters and on their model substrates” [4]. PMID:26981550

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

    PubMed

    Perz, Veronika; Bleymaier, Klaus; Sinkel, Carsten; Kueper, Ulf; Bonnekessel, Melanie; Ribitsch, Doris; Guebitz, Georg M

    2016-06-01

    The aliphatic-aromatic copolyester poly(butylene adipate-co-butylene terephthalate) (PBAT), also known as ecoflex, contains adipic acid, 1,4-butanediol and terephthalic acid and is proven to be compostable [1], [2], [3]). We describe here data for the synthesis and analysis of poly(butylene adipate-co-butylene terephthalate variants with different adipic acid:terephatalic acid ratios and 6 oligomeric PBAT model substrates. Data for the synthesis of the following oligomeric model substrates are described: mono(4-hydroxybutyl) terephthalate (BTa), bis(4-(hexanoyloxy)butyl) terephthalate (HaBTaBHa), bis(4-(decanoyloxy)butyl) terephthalate (DaBTaBDa), bis(4-(tetradecanoyloxy)butyl) terephthalate (TdaBTaBTda), bis(4-hydroxyhexyl) terephthalate (HTaH) and bis(4-(benzoyloxy)butyl) terephthalate (BaBTaBBa). Polymeric PBAT variants were synthesized with adipic acid:terephatalic acid ratios of 100:0, 90:10, 80:20, 70:30, 60:40 and 50:50. These polymeric and oligomeric substances were used as ecoflex model substrates in enzymatic hydrolysis experiments in the article "Substrate specificities of cutinases on aliphatic-aromatic polyesters and on their model substrates" [4]. PMID:26981550

  9. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... polyethylene has a minimum number average molecular weight of 1,200, as determined by high temperature vapor pressure osmometry; contains a maximum of 5 percent by weight of total oxygen; and has an acid value of...

  10. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... produced by the direct chlorination of polyethylene conforming to the density, maximum n-hexane extractable... percent in plastic articles prepared from polyvinyl chloride and/or from vinyl chloride...

  11. Protein adsorption and cell adhesion on nanoscale bioactive coatings formed from poly(ethylene glycol) and albumin microgels

    PubMed Central

    Scott, Evan A.; Nichols, Michael D.; Cordova, Lee H.; George, Brandon J.; Jun, Young-Shin; Elbert, Donald L.

    2008-01-01

    Late-term thrombosis on drug-eluting stents is an emerging problem that might be addressed using extremely thin, biologically-active hydrogel coatings. We report a dip-coating strategy to covalently link poly(ethylene glycol) (PEG) to substrates, producing coatings with <≈100 nm thickness. Gelation of PEG-octavinylsulfone with amines in either bovine serum albumin (BSA) or PEG-octaamine was monitored by dynamic light scattering (DLS), revealing the presence of microgels before macrogelation. NMR also revealed extremely high end group conversions prior to macrogelation, consistent with the formation of highly crosslinked microgels and deviation from Flory-Stockmayer theory. Before macrogelation, the reacting solutions were diluted and incubated with nucleophile-functionalized surfaces. Using optical waveguide lightmode spectroscopy (OWLS) and quartz crystal microbalance with dissipation (QCM-D), we identified a highly hydrated, protein-resistant layer with a thickness of approximately 75 nm. Atomic force microscopy in buffered water revealed the presence of coalesced spheres of various sizes but with diameters less than about 100 nm. Microgel-coated glass or poly(ethylene terephthalate) exhibited reduced protein adsorption and cell adhesion. Cellular interactions with the surface could be controlled by using different proteins to cap unreacted vinylsulfone groups within the coating. PMID:18771802

  12. Osmotic effects of polyethylene glycol.

    PubMed

    Schiller, L R; Emmett, M; Santa Ana, C A; Fordtran, J S

    1988-04-01

    Polyethylene glycol (PEG) has been used to increase the osmotic pressure of fluids used to cleanse the gastrointestinal tract. However, little is known about its osmotic activity. To investigate this activity systematically, solutions of PEG of differing molecular weights were made and subjected to measurement of osmolality by both freezing point depression and vapor pressure osmometry. Measured osmolality was increasingly greater than predicted from average molecular weight as PEG concentration increased. Measurement of sodium activity in NaCl/PEG solutions by means of an ion-selective electrode suggested that the higher than expected osmolality could be due in part to interactions that, in effect, sequestered water from the solution. Osmolality was consistently greater by freezing point osmometry than by vapor pressure osmometry. To determine which osmometry method reflected biologically relevant osmolality, normal subjects underwent steady-state total gut perfusion with an electrolyte solution containing 105 g/L of PEG 3350. This produced rectal effluent that was hypertonic by freezing point osmometry but isotonic by vapor pressure osmometry. Assuming that luminal fluid reaches osmotic equilibrium with plasma during total gut perfusion, this result suggests that the vapor pressure osmometer accurately reflects the biologically relevant osmolality of intestinal contents. We conclude that PEG exerts more of an osmotic effect than would be predicted from its molecular weight. This phenomenon may reflect interactions between PEG and water molecules that alter the physical chemistry of the solution and sequester water from the solution. PMID:3345895

  13. Maxillofacial prostheses of chlorinated polyethylene.

    PubMed

    May, P D

    1978-05-01

    There is clearly a need for maxillofacial prosthetic materials with improved properties. The chlorinated polyethylenes are thermoplastic elastomers which have particularly promising properties, and were used by us to prepare improved maxillofacial prostheses. Suitable CPE resins were compounded with other polymers and with pigments on a heated rubber mill to form thin sheets in a variety of shades. These were heated at 190 degrees C for 10 min and placed between heated linotype mold halves. The prosthesis was formed in a hand press. Sometimes heating and pressing were repeated. After cooling in water, the prosthesis was removed and hand-shaded with oil-soluble dyes. Physical properties were evaluated using standard techniques; skin irritation studies were conducted by 14-day insult patch tests on rabbits. Clinical evaluations were conducted on human volunteers. Parallel evaluations were conducted on commerically available materials for comparison. The CPE was superior to all of the three commerical materials in most properties, and comparable to the better of the three in the remaining properties. On balance, CPE was significantly superior. Early results indicate that the materials and techniques required are easily handled in the dental lab and that the final prosthesis has excellent aesthetic and patient acceptability. PMID:670262

  14. Charge packets modeling in polyethylene

    NASA Astrophysics Data System (ADS)

    Baudoin, F.; Laurent, C.; Teyssedre, G.; Le Roy, S.

    2014-04-01

    Charge packets in insulating polymers have been reported by many groups within the last two decades, especially in polyethylene-based materials. They consist in a pulse of net charge that remains in the form of a pulse as it crosses the insulation. In spite of a variety of characteristics depending on material properties and experimental conditions, one of the puzzling aspects of the packets is their repetitive character until they eventually die away. Several theories have been proposed to explain their formation and propagation. Two of them have the advantage of simplicity and of being physically based, being the existence of an hysteresis loop in the injection mechanism or a negative differential mobility of carriers with the electric field. Based on these descriptions, some progress has been done recently by discussing the shape of the packets during their propagation but none of the concepts has been incorporated into a transport model to describe the full evolution from the packet generation to their vanishing. Here, we used a simplified transport model featuring bipolar charge injection and transport coupled to specific conditions in charge injection or carrier mobility to reproduce experimental results. One of the salient features of the results is that both models are able to reproduce the repetitive character and the dying away of the packets that appear to be linked with the internal field distribution modulated by a bipolar space charge.

  15. Interchain electron states in polyethylene

    NASA Astrophysics Data System (ADS)

    Serra, S.; Tosatti, E.; Iarlori, S.; Scandolo, S.; Santoro, G.

    2000-08-01

    We present a theoretical study of the nature of the lowest empty conduction-band states in crystalline polyethylene (PE), conducted through density-functional electronic structure calculations. Results reveal that the wave function of the conduction-band edge is of interchain character, as opposed to the intrachain character of all the filled valence-band states. Thus, while a hole added to neutral PE will mainly belong to the PE chain backbone bonds, an added electron in PE will mostly reside between the chains, and far from the existing bonds. Moreover, the added electron state charge centroid is predicted to move further out from the chain backbone towards the low-density interstitial region, if and when the chains are pried apart. This suggests that injected electrons will naturally flow to low-density regions inside real PE, and that the experimentally established propensity of PE to expel electrons out of the bulk, should be directly related to the interchain nature of the conduction states.

  16. Acute polyethylene fracture in an uncemented acetabular cup

    PubMed Central

    Gross, Allan E.; Dust, William N.

    1997-01-01

    The smaller acetabular components used in total hip replacement may have a polyethylene liner that is too thin, resulting in higher polyethylene stress and an increased potential for wear. The authors present a case that highlights the problem of acute polyethylene fracture. To compensate for the thinness of the polyethylene, the authors recommend the use of a smaller head size to allow polyethylene thickness of at least 8 mm. PMID:9267302

  17. Development of biodegradable and injectable macromers based on poly(ethylene glycol) and diacid monomers.

    PubMed

    Kim, Jinku; Yaszemski, Michael J; Lu, Lichun

    2009-09-15

    Novel biodegradable injectable poly(ethylene glycol)-(PEG) based macromers were synthesized by reacting low-molecular weight PEG (MW: 200) and dicarboxylic acids such as sebacic acid or terephthalic acid. Chemical structures of the resulting polymers were confirmed by Fourier transform infrared (FTIR) and nuclear magnetic resonance (NMR) spectroscopy characterizations. Differential scanning calorimetry (DSC) showed that these polymers were completely amorphous above room temperature. After photopolymerization, dynamic elastic shear modulus of the crosslinked polymers was up to 1.5 MPa and compressive modulus was up to 2.2 MPa depending on the polymer composition. The in vitro degradation study showed that mass losses of these polymers were gradually decreased over 23 weeks of period in simulated body fluid. By incorporating up to 30 wt % of 2-hydroxyethyl methylmethacrylate (HEMA) into the crosslinking network, the dynamic elastic modulus and compressive modulus was significantly increased up to 7.2 and 3.2 MPa, respectively. HEMA incorporation also accelerated the degradation as indicated by substantially higher mass loss of up to 27% after 20 weeks of incubation. Cytocompatability studies using osteoblasts and neural cells revealed that cell metabolic activity on these polymers with or without HEMA was close to the control tissue culture polystyrene. The PEG-based macromers developed in this study may be useful as scaffolds or cell carriers for tissue engineering applications. PMID:18655146

  18. Polyethylene glycol enhanced protein refolding.

    PubMed

    Cleland, J L; Builder, S E; Swartz, J R; Winkler, M; Chang, J Y; Wang, D I

    1992-09-01

    Previous studies on the refolding of recombinant bovine carbonic anhydrase B (CAB) indicated that polyethylene glycol (PEG) significantly enhanced the recovery of active protein by reducing aggregation. To further test the ability of PEG to enhance refolding, three recombinant human proteins, deoxyribonuclease (rhDNAse), tissue plasminogen activator (rhtPA), and interferon-gamma (rhIFN-gamma) were refolded in the presence of PEG (3350 MW). rhDNAse produced from CHO cells was denatured in 7.2 M urea and refolded by rapid dilution to 4.0 M urea and 0.20 mg/ml protein. When a final PEG to rhDNAse molar ratio of 5 to 1 (0.1 milligram PEG, 3350 MW) was used in the dilution buffer, refolding was improved by 30% to yield complete recovery of active protein. Impure E. coli derived inclusion body preparations of rhDNAse were solubilized in 8 M urea and refolded by dilution to 4 M urea and 0.10 mg/ml protein. Refolding with a dilution buffer which yielded a final PEG to rhDNAse molar ratio of 10 to 1 (0.1 milligram PEG, 3350 MW) resulted in a three-fold increase in the recovery of active protein. When PEG was used in the dilution buffer, aggregation of rhDNAse did not occur during refolding in either case. rhtPA produced from CHO cells was denatured in 5 M guanidine hydrochloride (GuHCl) and refolded by rapid dilution to 0.10 M GuHCl and 0.20 mg/ml protein.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:1368998

  19. Catastrophic Failure of the Acetabular Polyethylene Liner in Ceramic-on-Polyethylene Total Hip Arthroplasty

    PubMed Central

    Manzano, Givenchy; Levin, Rayna A. C.; Mayor, Michael B.; Schwarzkopf, Ran

    2014-01-01

    Introduction: Catastrophic polyethylene failure is a rare complication of ceramic-on-polyethylene total hip arthroplasty due to the favorable tribological characteristics of ceramic. Failure of the polyethylene liner can be disastrous, increasing periprosthetic osteolysis, metallosis, and risk of dislocation. Complications associated with ceramic-on-polyethylene articulations have been studied extensively, however, only few reports have described its catastrophic wear. We report such a case of complete wear of the acetabular liner in a ceramic-on-polyethylene prosthesis in a 57-year adult male. Case Report: A 57-year adult male with a history of bilateral total hip arthroplasty presented to our institution with bilateral hip pain worst on the right. Range of motion was limited by pain on the right hip at the extremes of motion. Radiographs revealed severe osteolysis, heterotopic ossification, complete wear of the acetabular liner, bony impingement of the femoral greater trochanter on the acetabular rim and superior migration of the femoral head. All findings were confirmed intraoperatively. Revision of the acetabular components was performed, which successfully alleviated the patient’s symptoms. Conclusion: Failure of the ceramic-on-polyethylene liner in our patient is due to the use of a non-cross linked polyethylene liner, a highly active lifestyle, and poor follow up. Arthroplasty surgeons should be aware of this complication especially in highly active patients with a conventional polyethylene liner and chronic hip pain. PMID:27298960

  20. Polymeric compositions incorporating polyethylene glycol as a phase change material

    DOEpatents

    Salyer, Ival O.; Griffen, Charles W.

    1989-01-01

    A polymeric composition comprising a polymeric material and polyethylene glycol or end-capped polyethylene glycol as a phase change material, said polyethylene glycol and said end-capped polyethylene glycol having a molecular weight greater than about 400 and a heat of fusion greater than about 30 cal/g; the composition is useful in making molded and/or coated materials such as flooring, tiles, wall panels and the like; paints containing polyethylene glycols or end-capped polyethylene glycols are also disclosed.

  1. Elongational rheology of polyethylene melts

    NASA Astrophysics Data System (ADS)

    Seyfzadeh, Bijan

    Elongational melt flow behavior is an important and fundamental concept underlying many industrial plastics operations which involve a rapid change of shape as for example fiber spinning and stretching, bottle blow molding, and film blowing and stretching. Under high process loads polymeric materials experience enormous stresses causing the molecular structure to gain considerable orientation. This event has significant effects on the melt flow behavior and can be measured in terms of elongational viscosity and changes in enthalpy and entropy. Different polymeric materials with unique molecular characteristics are expected to respond uniquely to the elongational deformation; hence, molecular parameters such as molecular weight and degree of branching were related to the measurable elongational flow variables. Elongational viscosities were measured for high and low density polyethylenes using an advanced capillary extrusion rheometer fitted with semi-hyperbolic dies. Said dies establish a purely elongational. flow field at constant elongational strain rate. The elongational viscosities were evaluated under influence of process strain rate, Hencky strain (natural logarithm of area reduction of the extrusion die), and temperature. Enthalpy and entropy changes associated with the orientation development of semi-hyperbolic processed melts were also determined. Results showed that elongational viscosities were primarily affected by differences in weight average molecular weight rather than degree of branching. This effect was process strain rate as well as temperature dependent. An investigation of melt relaxation and the associated first decay time constants revealed that with increasing strain rate the molecular field of the melt asymptotically gained orientation in approaching a limit. As a result of this behavior molecular uniqueness vanished at high process strain rates, yielding to orientation development and the associated restructuring of the melt's molecular

  2. Recent advances in polyethylene separator technology

    NASA Astrophysics Data System (ADS)

    Weighall, M. J.

    The well known technical and production benefits of polyethylene separator materials over other separator materials have prompted a dramatic increase in polyethylene separator usage in recent years. Separator trends in the United States from 1980 to 1996, and in Europe from 1987 to 1992, are shown. The manufacturing process for polyethylene separators is outlined, with particular emphasis on the latest advances in manufacturing technology. These improvements have resulted in a higher quality product, and also benefit the environment because of the sophisticated oil extraction and solvent recovery system. The product quality improvements resulting from the latest manufacturing technology include consistent conformance to dimensional specifications, low electrical resistance, close control of residual oil content, virtual elimination of pinholes, and good running properties on the battery manufacturers' plate enveloping machines. The material can also be manufactured with a very thin backweb to reduce electrical resistance still further.

  3. Thorium terephthalates coordination polymers synthesized in solvothermal DMF/H2O system.

    PubMed

    Falaise, Clément; Charles, Jean-Sébastien; Volkringer, Christophe; Loiseau, Thierry

    2015-03-01

    A series of thorium-based terephthalates have been solvothermaly synthesized in N,N-dimethylformamide (DMF) with different amounts of water and various temperatures (100-150 °C). Without the addition of water, the Th-H2bdc-DMF system gives rise to the formation of two phases, Th(bdc)2(DMF)2 (1) and Th6O4(OH)4(H2O)6(bdc)6·6DMF·12H2O (3) (bdc = 1,4-benzenedicarboxylate or terephthalate). Their structures are built up of isolated thorium centers ThO8(DMF)2 for (1) and the hexanuclear core Th6O4(OH)4(H2O)6 for (3). The latter adopts the UiO-66 metal-organic framework topology and exhibits a very high porosity for an actinides-based porous material (BET surface up to 730(6) m(2)·g(-1)). The synthesis of (3) is also favored upon adding water. However, for pure aqueous solutions or for a very low amount of water, a third solid Th(bdc)2 (2) crystallizes and contains thorium monomers ThO8. The main similitude with the parent system dedicated to tetravalent uranium concerns the possibility to stabilize the An6O8(H2O)6 core by terephthalate linkers and to reproduce An(bdc)2(DMF)2 for both actinides U(4+) and Th(4+). The thermal treatment of the latter shows a structural transition into the crystalline Th(bdc)2 (2) solid. PMID:25668215

  4. Tensile Deformation of Polyethylenes: Crystallinity Effects

    NASA Astrophysics Data System (ADS)

    Crist, Buckley; Metaxas, Costas

    2004-03-01

    The crystalline fraction of polyethylene can be reduced by increasing the cooling rate, the molecular weight or the fraction of comonomer. All three methods have been used in this study of tensile deformation which shows that true stress - true strain behavior depends systematically on morphology. The dependence of uniaxial yield stress on crystal thickness is well understood in terms of dislocation nucleation. Post yield flow is dominated by the strain hardening rate that is larger in polyethylenes of lower crystallinity. Noncrystalline polymer evidently reduces the plastic compliance while providing for elastic (reversible) strains. These observations are examined in terms of old and new theories for deformation of semicrystalline polymers.

  5. Polyethylene glycol-electrolyte solution (PEG-ES)

    MedlinePlus

    Polyethylene glycol-electrolyte solution (PEG-ES) is used to empty the colon (large intestine, bowel) before a ... Polyethylene glycol-electrolyte solution (PEG-ES) comes as a powder to mix with water and take by ...

  6. 40 CFR 721.6493 - Amidoamine modified polyethylene glycol (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Amidoamine modified polyethylene... Specific Chemical Substances § 721.6493 Amidoamine modified polyethylene glycol (generic). (a) Chemical... as an amidoamine modified polyethylene glycol (PMN P-99-0645) is subject to reporting under...

  7. 40 CFR 721.6493 - Amidoamine modified polyethylene glycol (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Amidoamine modified polyethylene... Specific Chemical Substances § 721.6493 Amidoamine modified polyethylene glycol (generic). (a) Chemical... as an amidoamine modified polyethylene glycol (PMN P-99-0645) is subject to reporting under...

  8. 40 CFR 721.6493 - Amidoamine modified polyethylene glycol (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Amidoamine modified polyethylene... Specific Chemical Substances § 721.6493 Amidoamine modified polyethylene glycol (generic). (a) Chemical... as an amidoamine modified polyethylene glycol (PMN P-99-0645) is subject to reporting under...

  9. 21 CFR 178.3760 - Polyethylene glycol (400) monolaurate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene glycol (400) monolaurate. 178.3760... SANITIZERS Certain Adjuvants and Production Aids § 178.3760 Polyethylene glycol (400) monolaurate. Polyethylene glycol (400) monolaurate containing not more than 0.1 percent by weight of ethylene...

  10. 21 CFR 178.3760 - Polyethylene glycol (400) monolaurate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene glycol (400) monolaurate. 178.3760 Section 178.3760 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES... Production Aids § 178.3760 Polyethylene glycol (400) monolaurate. Polyethylene glycol (400)...

  11. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  12. 21 CFR 178.3760 - Polyethylene glycol (400) monolaurate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene glycol (400) monolaurate. 178.3760... SANITIZERS Certain Adjuvants and Production Aids § 178.3760 Polyethylene glycol (400) monolaurate. Polyethylene glycol (400) monolaurate containing not more than 0.1 percent by weight of ethylene...

  13. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface of articles intended for use in contact...

  14. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  15. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  16. 40 CFR 721.6493 - Amidoamine modified polyethylene glycol (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Amidoamine modified polyethylene... Specific Chemical Substances § 721.6493 Amidoamine modified polyethylene glycol (generic). (a) Chemical... as an amidoamine modified polyethylene glycol (PMN P-99-0645) is subject to reporting under...

  17. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  18. 40 CFR 721.6493 - Amidoamine modified polyethylene glycol (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Amidoamine modified polyethylene... Specific Chemical Substances § 721.6493 Amidoamine modified polyethylene glycol (generic). (a) Chemical... as an amidoamine modified polyethylene glycol (PMN P-99-0645) is subject to reporting under...

  19. 21 CFR 178.3760 - Polyethylene glycol (400) monolaurate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene glycol (400) monolaurate. 178.3760... SANITIZERS Certain Adjuvants and Production Aids § 178.3760 Polyethylene glycol (400) monolaurate. Polyethylene glycol (400) monolaurate containing not more than 0.1 percent by weight of ethylene...

  20. Computational method for analysis of polyethylene biodegradation

    NASA Astrophysics Data System (ADS)

    Watanabe, Masaji; Kawai, Fusako; Shibata, Masaru; Yokoyama, Shigeo; Sudate, Yasuhiro

    2003-12-01

    In a previous study concerning the biodegradation of polyethylene, we proposed a mathematical model based on two primary factors: the direct consumption or absorption of small molecules and the successive weight loss of large molecules due to β-oxidation. Our model is an initial value problem consisting of a differential equation whose independent variable is time. Its unknown variable represents the total weight of all the polyethylene molecules that belong to a molecular-weight class specified by a parameter. In this paper, we describe a numerical technique to introduce experimental results into analysis of our model. We first establish its mathematical foundation in order to guarantee its validity, by showing that the initial value problem associated with the differential equation has a unique solution. Our computational technique is based on a linear system of differential equations derived from the original problem. We introduce some numerical results to illustrate our technique as a practical application of the linear approximation. In particular, we show how to solve the inverse problem to determine the consumption rate and the β-oxidation rate numerically, and illustrate our numerical technique by analyzing the GPC patterns of polyethylene wax obtained before and after 5 weeks cultivation of a fungus, Aspergillus sp. AK-3. A numerical simulation based on these degradation rates confirms that the primary factors of the polyethylene biodegradation posed in modeling are indeed appropriate.

  1. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene, oxidized. 177.1620 Section 177.1620 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as...

  2. 21 CFR 177.1620 - Polyethylene, oxidized.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene, oxidized. 177.1620 Section 177.1620 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as...

  3. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Oxidized polyethylene. 172.260 Section 172.260 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Coatings, Films and Related Substances...

  4. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Oxidized polyethylene. 172.260 Section 172.260 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Coatings, Films and Related Substances...

  5. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Polyethylene. 573.780 Section 573.780 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food...

  6. 21 CFR 573.780 - Polyethylene.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Polyethylene. 573.780 Section 573.780 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food...

  7. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Oxidized polyethylene. 172.260 Section 172.260 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Coatings, Films and Related...

  8. POLYETHYLENE ENCAPSULATES FOR HAZARDOUS WASTE DRUMS

    EPA Science Inventory

    This capsule report summarizes studies of the use of polyethylene (P.E.) for encapsulating drums of hazardous wastes. Flat PE sheet is welded to roto moded PE containers which forms the encapsulates. Plastic pipe welding art was used, but the prototype welding apparatus required ...

  9. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Oxidized polyethylene. 172.260 Section 172.260 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Coatings, Films and Related Substances...

  10. DNP with Trityl Radicals in Deuterated Polyethylene

    NASA Astrophysics Data System (ADS)

    Wang, Li; Meyer, W.; Berlin, A.; Herick, J.; Hess, C.; Reicherz, G.

    2016-02-01

    Chemically doping with trityl radicals was performed in fully deuterated polyethylene. The behavior of paramagnetic centers has been investigated by ESR X-band spectrometer. The highest deuteron polarization was 8% at 2.5 T and 1 K with a spin concentration of 3 × 1019 spins/g.

  11. Herbicide dissipation from low density polyethylene mulch

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Field and laboratory studies were conducted to examine herbicide dissipation when applied to low density polyethylene (LDPE) mulch for dry scenarios vs. washing off with water. In field studies, halosulfuron, paraquat, carfentrazone, glyphosate, and flumioxazin were applied to black 1.25-mil LDPE at...

  12. Preservation of Mercury in Polyethylene Containers.

    ERIC Educational Resources Information Center

    Piccolino, Samuel Paul

    1983-01-01

    Reports results of experiments favoring use of 0.5 percent nitric acid with an oxidant (potassium dichromate or potassium permanganate) to preserve samples in polyethylene containers for mercury analysis. Includes procedures used and statistical data obtained from the experiments. (JN)

  13. STRESS CRACK TESTING OF POLYETHYLENE GEOMEMBRANES

    EPA Science Inventory

    The sensitivity of high density polyethylene (HDPE) geomembranes to stress cracking is evaluated under accelerated conditions at a constant stress. he test specimens are according to ASTM D-1822, and are of the dumbbell shape with a constant length in the central section. he acce...

  14. Modification of N-Methyl-N-Nitrosourea initiated bladder carcinogenesis in Wistar rats by terephthalic acid

    SciTech Connect

    Cui Lunbiao; Shi Yuan; Dai Guidong; Pan Hongxin; Chen Jianfeng; Song Ling; Wang Shouling; Chang, Hebron C.; Sheng Hongbing; Wang Xinru . E-mail: xrwang@njmu.edu.cn

    2006-01-15

    The effect of terephthalic acid (TPA) on urinary bladder carcinogenesis was examined. Male Wistar rats were initiated by injection of N-Methyl-N-Nitrosourea (MNU) (20 mg/kg b.w. ip) twice a week for 4 weeks, then given basal diet containing 5% TPA, 5% TPA plus 4% Sodium bicarbonate (NaHCO{sub 3}) or 1% TPA for the next 22 weeks, and then euthanized. 5% TPA treatment induced a high incidence of urinary bladder calculi and a large amount of precipitate. Though 5% TPA plus 4% Sodium bicarbonate (NaHCO{sub 3}) and 1% TPA treatment did not induce urinary bladder calculi formation, they resulted in a moderate increase in urinary precipitate. Histological examination of urinary bladder revealed that MNU-5% TPA treatment resulted in a higher incidence of simple hyperplasia, papillary or nodular hyperplasia (PN hyperplasia), papilloma and cancer than MNU control. MNU-5% TPA plus 4% Sodium bicarbonate (NaHCO{sub 3}) and 1% TPA treatment increased slightly the incidence of simple hyperplasia and PN hyperplasia (not statistically significant). The major elements of the precipitate are phosphorus, potassium, sulfur, chloride, calcium and TPA. The present study indicated that the calculi induced by TPA had a strong promoting activity on urinary bladder carcinogenesis and the precipitate containing calcium terephthalate (CaTPA) may also have weak promoting activity on urinary bladder carcinogenesis.

  15. Application of Universal Stress Proteins in Probing the Dynamics of Potent Degraders in Complex Terephthalate Metagenome

    PubMed Central

    Mbah, Andreas N.; Isokpehi, Raphael D.

    2013-01-01

    The culture-independent strategies to study microbial diversity and function have led to a revolution in environmental genomics, enabling fundamental questions about the distribution of microbes and their influence on bioremediation to be addressed. In this research we used the expression of universal stress proteins as a probe to determine the changes in degrading microbial population from a highly toxic terephthalate wastewater to a less toxic activated sludge bioreactor. The impact of relative toxicities was significantly elaborated at the levels of genus and species. The results indicated that 23 similar prokaryotic phyla were represented in both metagenomes irrespective of their relative abundance. Furthermore, the following bacteria taxa Micromonosporaceae, Streptomyces, Cyanothece sp. PCC 7822, Alicyclobacillus acidocaldarius, Bacillus halodurans, Leuconostoc mesenteroides, Lactococcus garvieae, Brucellaceae, Ralstonia solanacearum, Verminephrobacter eiseniae, Azoarcus, Acidithiobacillus ferrooxidans, Francisella tularensis, Methanothermus fervidus, and Methanocorpusculum labreanum were represented only in the activated sludge bioreactor. These highly dynamic microbes could serve as taxonomic biomarkers for toxic thresholds related to terephthalate and its derivatives. This paper, highlights the application of universal stress proteins in metagenomics analysis. Dynamics of microbial consortium of this nature can have future in biotechnological applications in bioremediation of toxic chemicals and radionuclides. PMID:24151583

  16. Macrophage phagocytosis of polyethylene particulate in vitro.

    PubMed

    Voronov, I; Santerre, J P; Hinek, A; Callahan, J W; Sandhu, J; Boynton, E L

    1998-01-01

    In this study, an in vitro model has been developed to examine the interactions of macrophages with ultrahigh molecular-weight polyethylene (UHMWPE) and high-density polyethylene (HDPE) particles. Polyethylene particles are the major constituent of the material debris formed as a result of orthopedic implant wear. However, the study of polyethylene particle interactions with cells has been limited. UHMWPE (18-20 microns) and HDPE (4-10 microns) were suspended in soluble collagen type I and subsequently solidified on glass coverslips. The particle chemistry was characterized by Fourier transform infra-red spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS). Mouse cell line macrophages (IC-21) were established on the collagen-particle substrata and maintained for up to 24 h. The response of the cells to the particles was examined by light and transmission electron microscopy (LM and TEM), as well as by scanning electron microscopy (SEM), and compared to cells on control collagen surfaces without particles. Histological analysis of the samples revealed that the macrophages surrounded larger particles (18-20 microns) and the cells appeared to be attached to the surface of the particles, and the smaller particles (4-10 microns) had been phagocytosed within 2 h. Inflammatory cytokines (TNF-alpha, IL-1 alpha, IL-1 beta, and IL-6), lysosomal enzymes (beta-galactosidase and hexosaminidase), and prostaglandin E2 were released into the medium, and IL-1 alpha, IL-1 beta, PGE2, beta-galactosidase, and hexosaminidase levels were significantly increased over collagen control values. The results demonstrate active phagochemotaxis by macrophages for wear particulates and validate this model as a means of studying the specific in vitro interactions of polyethylene with cells. PMID:9429095

  17. ON THE UV CURABILITY AND MECHANICAL PROPERTIES OF NOVEL BINDER SYSTEMS DERIVED FROM POLY(ETHYLENE TEREPHTHALATE) PET WASTE FOR SOLVENTLESS MAGNETIC TAPE MANUFACTURING: ACRYLATED OLIGOESTERS. (R827121)

    EPA Science Inventory

    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...

  18. NOVEL BINDER SYSTEMS DERIVED FROM POLY(ETHYLENE TEREPHTHALATE) PET WASTE FOR SOLVENTLESS MAGNETIC TAPE MANUFACTURING: INVESTIGATION ON THE MECHANICAL PROPERTIES OF THE METHACRYLATED OLIGOESTERS. (R826728)

    EPA Science Inventory

    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...

  19. ON THE UV CURABILITY AND MECHANICAL PROPERTIES OF NOVEL BINDER SYSTEMS DERIVED FROM POLY(ETHYLENE TEREPHTHALATE) PET WASTE FOR SOLVENTLESS MAGNETIC TAPE MANUFACTURING: ACRYLATED OLIGOESTERS. (R826728)

    EPA Science Inventory

    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...

  20. ON THE UV CURABILITY AND MECHANICAL PROPERTIES OF NOVEL BINDER SYSTEMS DERIVED FROM POLY(ETHYLENE TEREPHTHALATE) PET WASTE FOR SOLVENTLESS MAGNETIC TAPE MANUFACTURING: METHACRYLATED OLIGOESTERS. (R827121)

    EPA Science Inventory

    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...

  1. NOVEL BINDER SYSTEMS DERIVED FROM POLY(ETHYLENE TEREPHTHALATE) PET WASTE FOR SOLVENTLESS MAGNETIC TAPE MANUFACTURING I: INVESTIGATION OF THE MECHANICAL PROPERTIES OF THE ACRYLATED OLIGOMERS. (R826728)

    EPA Science Inventory

    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...

  2. Aminolysis of polyethylene terephthalate surface along with in situ synthesis and stabilizing ZnO nanoparticles using triethanolamine optimized with response surface methodology.

    PubMed

    Poortavasoly, Hajar; Montazer, Majid; Harifi, Tina

    2016-01-01

    This research concerned the simultaneous polyester surface modification and synthesis of zinc oxide nano-reactors to develop durable photo-bio-active fabric with variable hydrophobicity/hydrophilicity under sunlight. For this purpose, triethanolamine (TEA) was applied as a stabilizer and pH adjusting chemical for the aminolysis of polyester surface and enhancing the surface reactivity along with synthesis and deposition of ZnO nanoparticles on the fabric. Therefore, TEA played a crucial role in providing the alkaline condition for the preparation of zinc oxide nanoparticles and acting as stabilizer controlling the size of the prepared nanoparticles. The stain-photodegradability regarded as self-cleaning efficiency, wettability and weight change under the process was optimized based on zinc acetate and TEA concentrations, using central composite design (CCD). Findings also suggested the potential of the prepared fabric in inhibiting Staphylococcus aureus and Escherichia coli bacteria growth with greater than 99.99% antibacterial efficiency. Besides, the proposed treatment had no detrimental effect on tensile strength and hand feeling of the polyester fabric. PMID:26478337

  3. Morphological changes in semicrystalline poly(ether ether ketone) and poly(ethylene terephthalate) during heating and structures of blends with poly(ether imide)

    SciTech Connect

    Jonas, A.M.; Russell, T.P.; Yoon, D.Y.

    1995-12-01

    Structural changes occurring during heating of cold crystallized PEEK and PET have been studied by real-time x-ray scattering using synchrotron radiation. Rapid melting/recrystallization is found when the semicrystalline PEEK and PET samples are heated above the previous highest annealing temperatures, Such melting/recrystallization results in irreversible increases in the lamellar long period, the crystal thickness and the density difference between the crystalline and amorphous regions. Throughout the entire temperature range up to the melting point, the linear crystallinity of lamellar stacks remains nearly constant around 0.3. The fact that both PEEK and PET form miscible blends with poly(ether imide) (PEI) in amorphous melts has been utilized to identify and to investigate the noncrystalline inter-lamellar region in the semicrystalline samples. For the semicrystalline blends of PEEK/PEI, both the small-angle x-ray scattering and dielectric loss measurements show that only a small amount of PEI is mixed in the inter-lamellar region. The majority of PEI, expelled from the lamellar stacks, is totally demixed from PEEK, demonstrating that the inter-lamellar region of semicrystalline PEEK is significantly different from the random amorphous melt. Therefore, the level of linear crystallinity and the miscibility characteristics indicate the presence of thick ordered interfacial layer on the lamellar surface, most likely due to the presence of rigid aromatic groups in PEEK and PET chains.

  4. The effect of reaction processing on the physical, morphological, and barrier properties of poly(ethylene 2,6-naphthalene dicarboxylate)/poly(ethylene terephthalate) blends

    NASA Astrophysics Data System (ADS)

    Uthaisombut, Rujida

    PET/PEN blends have been considered as a new material, combining the economic advantages of PET with the high barrier and thermal properties of PEN, which can extend the limitation of PET packaging applications. However, PET and PEN are inherently incompatible. Extrusion of PET/PEN blends above the melting temperature of both polymers results in transesterification, which was shown to enhance the miscibility of the blend and improve both the clarity and barrier properties of the resultant films. This research focused on the study of the effect of the processing conditions and the blend composition on the transesterification reaction. In addition, the effect of degree of transesterification, the blend composition, and the orientation on the blend characteristics was also studied. The results showed that the primary factors controlling the transesterification reaction were blending time and temperature, whereas the composition of the blends was found to have little or no effect on the interchange reaction. The PET/PEN blends with a degree of transesterification of at least 6% were miscible, homogeneous and optically clear. Further the transesterification reaction had less of an effect on the Tg, the barrier, and the mechanical properties. However, the Tm, % crystallinity, density, and molecular weight average were dependent on the degree of transesterification, regardless of how this degree of transesterification was achieved. The blend composition was a very important factor controlling the thermal, mechanical, and barrier properties of the blends. A depression of the T m, % crystallinity, and molecular weight was found, when a small amount of PEN was added to the PET rich phase, or vice versa. The Tm, % crystallinity and molecular weight average were lowest, when the PEN composition was 40--50 mole %. Moreover, the density of the blends decreased, as the PEN composition increased. However, the Tg, the gas barrier properties and the tensile strength of the blends improved when the PEN composition increased. Orientation process enhanced the barrier and the mechanical properties of the blend films. The water vapor, the oxygen, and the carbon dioxide barrier properties of the PET/PEN blend films improved 1.5--2 times, as the blend films were 3 x 3 biaxially oriented. The tensile strength of the oriented blend films was 4 times greater than that of the non-oriented blend films. Moreover, oriented PEN, and the oriented blend films were flexible, while the non-oriented films were very brittle.

  5. Gene Silencing In Human Aortic Smooth Muscle Cells Induced by PEI siRNA Complexes Released From Dip-Coated Electrospun Poly(ethylene Terephthalate) Grafts

    PubMed Central

    Nabzdyk, Christoph S.; Chun, Maggie; Oliver-Allen, Hunter; Pathan, Saif G.; Phaneuf, Matthew D.; You, Jin-Oh; Pradhan-Nabzdyk, Leena; LoGerfo, Frank W.

    2014-01-01

    An excessive tissue response to prosthetic arterial graft material leads to intimal hyperplasia (IH), the leading cause of late graft failure. Seroma and abnormal capsule formation may also occur after prosthetic material implantation. The matricellular protein Thrombospondin-2 (TSP-2) has shown to be upregulated in response to biomaterial implantation. This study evaluates the uptake and release of small interfering RNA (siRNA) from unmodified and surface functionalized electrospun PET graft materials. ePET graft materials were synthesized using electrospinning technology. Subsets of the ePET materials were then chemically modified to create surface functional groups. Unmodified and surface-modified ePET grafts were dip-coated in siRNAs alone or siRNAs complexed with transfection reagents polyethyleneimine (PEI) or Lipofectamine RNAiMax. Further, control and TSP-2 siRNA-PEI complex treated ePET samples were placed onto a confluent layer of human aortic smooth muscle cells (AoSMCs). Complexation of all siRNAs with PEI led to a significant increase in adsorption to unmodified ePET. TSP-2 siRNA-PEI released from unmodified-ePET silenced TSP-2 in AoSMC. Regardless of the siRNA-PEI complex evaluated, AoSMC migrated into the ePET. siRNA-PEI complexes delivered to AoSMC from dip-coated ePET can result in gene knock-down. This methodology for siRNA delivery may improve the tissue response to vascular and other prosthetics. PMID:24397987

  6. 21 CFR 177.1240 - 1,4-Cyclohexylene dimethylene terephthalate and 1,4-cyclohexylene dimethylene isophthalate...

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false 1,4-Cyclohexylene dimethylene terephthalate and 1,4-cyclohexylene dimethylene isophthalate copolymer. 177.1240 Section 177.1240 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES:...

  7. 21 CFR 177.1240 - 1,4-Cyclohexylene dimethylene terephthalate and 1,4-cyclohexylene dimethylene isophthalate...

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false 1,4-Cyclohexylene dimethylene terephthalate and 1,4-cyclohexylene dimethylene isophthalate copolymer. 177.1240 Section 177.1240 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR...

  8. 21 CFR 177.1240 - 1,4-Cyclohexylene dimethylene terephthalate and 1,4-cyclohexylene dimethylene isophthalate...

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false 1,4-Cyclohexylene dimethylene terephthalate and 1,4-cyclohexylene dimethylene isophthalate copolymer. 177.1240 Section 177.1240 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) INDIRECT FOOD...

  9. Controlled and high throughput fabrication of poly(trimethylene terephthalate) nanofibers via melt extrusion of immiscible blends

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Immiscible blends of cellulose acetate butyrate (CAB) and poly(trimethylene terephthalate) (PTT) were melt extruded through a two strand rod die. The extrudates were hot-drawn at the die exit at different draw ratios. PTT fibers were obtained by removal of the CAB matrix from the drawn extrudates, a...

  10. Atomic/Molecular Layer Deposition of Lithium Terephthalate Thin Films as High Rate Capability Li-Ion Battery Anodes.

    PubMed

    Nisula, Mikko; Karppinen, Maarit

    2016-02-10

    We demonstrate the fabrication of high-quality electrochemically active organic lithium electrode thin films by the currently strongly emerging combined atomic/molecular layer deposition (ALD/MLD) technique using lithium terephthalate, a recently found anode material for lithium-ion battery (LIB), as a proof-of-the-concept material. Our deposition process for Li-terephthalate is shown to well comply with the basic principles of ALD-type growth including the sequential self-saturated surface reactions, a necessity when aiming at micro-LIB devices with three-dimensional architectures. The as-deposited films are found crystalline across the deposition temperature range of 200-280 °C, which is a trait highly desired for an electrode material but rather unusual for hybrid inorganic-organic thin films. Excellent rate capability is ascertained for the Li-terephthalate films with no conductive additives required. The electrode performance can be further enhanced by depositing a thin protective LiPON solid-state electrolyte layer on top of Li-terephthalate; this yields highly stable structures with capacity retention of over 97% after 200 charge/discharge cycles at 3.2 C. PMID:26812433

  11. 21 CFR 177.1240 - 1,4-Cyclohexylene dimethylene terephthalate and 1,4-cyclohexylene dimethylene isophthalate...

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false 1,4-Cyclohexylene dimethylene terephthalate and 1,4-cyclohexylene dimethylene isophthalate copolymer. 177.1240 Section 177.1240 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES:...

  12. Molecular mechanism of viscoelasticity in aligned polyethylene

    NASA Astrophysics Data System (ADS)

    Hammad, Ali; Hasan, Hikmatyar; Swinburne, Thomas; Del Rosso, Stefano; Iannucci, Lorenzo; Sutton, Adrian

    2014-03-01

    Aligned polyethylene is used in industrial and medical applications due to its low density and high tensile strength. Extensive experimental work has been done to determine its mechanical properties, notably its viscoelasticity. However, the molecular processes that underlie these macroscopic properties are poorly understood. We develop a united atom model of aligned chains, in which intermolecular interactions are modelled by a Lennard-Jones potential, and the elastic energy within chains is modelled with harmonic springs. Using this simple model, we demonstrate the nucleation of solitons from chain ends, as one molecular chain is stretched with respect to another, and how load is transferred between chains in disregistry by intermolecular interactions. We develop an equation of motion for the movement of solitons along molecular chains, allowing us to replace a collection of aligned chains with a gas of solitons. Although solitons have been invoked to account for dielectric relaxation in crystalline regions of polyethylene, we believe this may be the first time they are discussed in the context of mechanical properties of aligned polyethylene.

  13. Extensional Flow Induced Crystallization of Polyethylene

    NASA Astrophysics Data System (ADS)

    Nicholson, David; Locker, C. Rebecca; Tsou, Andy; Rutledge, Gregory

    2014-03-01

    The majority of manufactured polyethylene is used in films mostly through the blown film fabrication process where extensional flow induced crystallization is a critical component in affecting the development of crystalline morphology and amorphous topology. In order to optimize the blown film performance, it is critical to understand the mechanism of extensional flow induced crystallization of polyethylene. Model high density polyethylene with a Mn of 20,000 g/mol and a PDI (polydispersity) of 2 and lower were synthesized by organometallic catalysts. Extensional flow induced crystallization of these materials was measured using the SER (Sentmanat Extensional Rheometer) either at a given rate with varying temperatures or vice versa. A continuum model was applied to analyze the flow induced crystallization data. All samples after extensional flow were quenched in ice water and the resulting morphology was characterized using SAXS and WAXS. The extensional rate was found to be effective in modifying morphology whereas the temperature was not; neither temperature nor strain rate affected the final film crystallinity. With an increase in extensional rate, crystallites became thinner and narrower with potentially higher connectivity which could lead to higher toughness.

  14. Grafting functional antioxidants on highly crosslinked polyethylene

    NASA Astrophysics Data System (ADS)

    Al-Malaika, S.; Riasat, S.; Lewucha, C.

    2016-05-01

    The problem of interference of antioxidants, such as hindered phenols, with peroxide-initiated crosslinking of polyethylene was addressed through the use of functional (reactive) graftable antioxidants (g-AO). Reactive derivatives of hindered phenol and hindered amine antioxidants were synthesised, characterised and used to investigate their grafting reactions in high density polyethylene; both non-crosslinked (PE) and highly peroxide-crosslinked (PEXa). Assessment of the extent of in-situ grafting of the antioxidants, their retention after exhaustive solvent extraction in PE and PEXa, and the stabilising performance of the grafted antioxidants (g-AO) in the polymer were examined and benchmarked against conventionally stabilised crosslinked & non-crosslinked polyethylene. It was shown that the functional antioxidants graft to a high extent in PEXa, and that the level of interference of the g-AOs with the polymer crosslinking process was minimal compared to that of conventional antioxidants which bear the same antioxidant function. The much higher level of retention of the g-AOs in PEXa after exhaustive solvent extraction, compared to that of the corresponding conventional antioxidants, accounts for their superior long-term thermal stabilising performance under severe extractive conditions.

  15. Polyethylene solidification of low-level wastes

    SciTech Connect

    Kalb, P.D.; Colombo, P.

    1985-02-01

    This topical report describes the results of an investigation on the solidification of low-level radioactive waste in polyethylene. Waste streams selected for this study included those which result from advanced volume reduction technologies (dry evaporator concentrate salts and incinerator ash) and those which remain problematic for solidification using contemporary agents (ion exchange resins). Four types of commercially available low-density polyethylenes were employed which encompass a range of processing and property characteristics. Process development studies were conducted to ascertain optimal process control parameters for successful solidification. Maximum waste loadings were determined for each waste and polyethylene type. Property evaluation testing was performed on laboratory-scale specimens to assess the potential behavior of actual waste forms in a disposal environment. Waste form property tests included water immersion, deformation under compressive load, thermal cycling and radionuclide leaching. Recommended waste loadings of 70 wt % sodium sulfate, 50 wt % boric acid, 40 wt % incinerator ash, and 30 wt % ion exchange resins, which are based on process control and waste form performance considerations are reported. 37 refs., 33 figs., 22 tabs.

  16. Lipase-catalyzed synthesis of a pure macrocyclic polyester from dimethyl terephthalate and diethylene glycol.

    PubMed

    Lavalette, Arnaud; Lalot, Thierry; Brigodiot, Maryvonne; Maréchal, Ernest

    2002-01-01

    The polymerization of dimethyl terephthalate and diethylene glycol by enzymic catalysis in toluene is described. The potential pi-pi interactions of the aromatic rings together with the relative flexibility of the diol segment have been regarded as synergy factors responsible for the formation of a pure cyclic compound. The so-called C2 macrocycle was characterized by (1)H and (13)C NMR, size-exclusion chromatography, differential scanning calorimetry, mass spectrometry, and X-ray diffraction on powder. Structurally speaking, it is made of two repeating units. The substitution of the central oxygen atom of the diol by -CH(2)- or -S- as well as the presence of ortho-substituents (-NH(2) or -NO(2)) on the phthalate were expected to disrupt the stacking of the phenyl groups more or less. PMID:11888304

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

    NASA Astrophysics Data System (ADS)

    Hwang, In-Tae; Jung, Chan-Hee; Kuk, In-Seol; Choi, Jae-Hak; Nho, Young-Chang

    2010-11-01

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

  18. Determination of the Thermal Decomposition Products of Terephthalic Acid by Using Curie-Point Pyrolyzer

    NASA Astrophysics Data System (ADS)

    Begüm Elmas Kimyonok, A.; Ulutürk, Mehmet

    2016-04-01

    The thermal decomposition behavior of terephthalic acid (TA) was investigated by thermogravimetry/differential thermal analysis (TG/DTA) and Curie-point pyrolysis. TG/DTA analysis showed that TA is sublimed at 276°C prior to decomposition. Pyrolysis studies were carried out at various temperatures ranging from 160 to 764°C. Decomposition products were analyzed and their structures were determined by gas chromatography-mass spectrometry (GC-MS). A total of 11 degradation products were identified at 764°C, whereas no peak was observed below 445°C. Benzene, benzoic acid, and 1,1‧-biphenyl were identified as the major decomposition products, and other degradation products such as toluene, benzophenone, diphenylmethane, styrene, benzaldehyde, phenol, 9H-fluorene, and 9-phenyl 9H-fluorene were also detected. A pyrolysis mechanism was proposed based on the findings.

  19. Formation mechanism of the secondary building unit in a chromium terephthalate metal-organic framework

    SciTech Connect

    Cantu Cantu, David; McGrail, B. Peter; Glezakou, Vassiliki Alexandra

    2014-09-18

    Based on density functional theory calculations and simulation, a detailed mechanism is presented on the formation of the secondary building unit (SBU) of MIL-101, a chromium terephthalate metal-organic framework (MOF). SBU formation is key to MOF nucleation, the rate-limiting step in the formation process of many MOFs. A series of reactions that lead to the formation of the SBU of MIL-101 is proposed in this work. Initial rate-limiting reactions form the metal cluster with three chromium (III) atoms linked to a central bridging oxygen. Terephthalate linkers play a key role as chromium (III) atoms are joined to linker carboxylate groups prior to the placement of the central bridging oxygen. Multiple linker addition reactions, which follow in different paths due to structural isomers, are limited by the removal of water molecules in the first chromium coordination shell. The least energy path is identified were all linkers on one face of the metal center plane are added first. A simple kinetic model based on transition state theory shows the rate of secondary building unit formation similar to the rate metal-organic framework nucleation. The authors are thankful to Dr. R. Rousseau for a critical reading of the manuscript. This research would not have been possible without the support of the Office of Fossil Energy, U.S. Department of Energy. This research was performed using EMSL, a national scientific user facility sponsored by the Department of Energy's Office of Biological and Environmental Research and the PNNL Institutional Computing (PIC) program located at Pacific Northwest National Laboratory.

  20. Comparison of Oxygen Gauche Effects in Poly(Oxyethylene) and Poly(ethylene terephtylene) Based on Quantum Chemistry Calculations

    NASA Technical Reports Server (NTRS)

    Jaffe, Richard; Han, Jie; Yoon, Do; Langhoff, Stephen R. (Technical Monitor)

    1997-01-01

    The so-called oxygen gauche effect in poly(oxyethylene) (POE) and its model molecules such as 1,2-dimethoxyethane (DME) and diglyme (CH3OC2H4OC2H4OCH3) is manifested in the preference for gauche C-C bond conformations over trans. This has also been observed for poly(ethylene terephthalate) (PET). Our previous quantum chemistry calculations demonstrated that the large C-C gauche population in DME is due, in part, to a low-lying tg +/- g+ conformer that exhibits a substantial 1,5 CH ... O attraction. New calculations will be described that demonstrate the accuracy of the original quantum chemistry calculations. In addition, an extension of this work to model molecules for PET will be presented. It is seen that the C-C gauche preference is much stronger in 1,2 diacetoxyethane than in DME. In addition, there exist low-lying tg +/- g+/- and g+/-g+/-g+/- conformers that exhibit 1,5 CH ... O attractions involving the carbonyl oxygens. It is expected that the -O-C-C-O- torsional properties will be quite different in these two polymers. The quantum chemistry results are used to parameterize rotational isomeric states models (RIS) and force fields for molecular dynamics simulations of these polymers.

  1. Bisoxalamide Clarifiers to Improve Optical Performance of Polyethylene Resins

    NASA Astrophysics Data System (ADS)

    Wang, Lin; Hill, Martin; Santos, Nestor, Jr.; Banks, Andrew; Huang, Jessica; Keene, Ellen; Keaton, Rich

    The use of special nucleating agents, often referred to as clarifying agents, to improve optical performance of polyethylene is not widely used in the industry. A series of bisoxalamide compounds were synthesized and mixed with linear low density polyethylene (LLDPE) to test clarification effects. In this talk, we will discuss structure/property relationship of these molecules on optical and thermal properties of LLDPE. Bisoxalamide clarifiers to improve optical performance of polyethylene resins.

  2. The yield behavior of polyethylene tubes subjected to biaxial loadings

    NASA Technical Reports Server (NTRS)

    Semeliss, M.; Wong, R.; Tuttle, M.

    1990-01-01

    High-density polyethylene is subjected to biaxial states of stress to examine the yield behavior of the semicrystalline thermoplastic under constant octahedral shear-stress rates. Combinations of internal pressures and axial loads are applied to thin-walled tubes of polyethylene, and the strain response in the axial and hoop directions are measured. The polyethylene specimens are found to be anisotropic, and the experimental measurements are compared to yield criteria that are applicable to isotropic and anisotropic materials.

  3. Radioprotection by polyethylene glycol-protein complexes in mice

    SciTech Connect

    Gray, B.H.; Stull, R.W.

    1983-03-01

    Polyethylene glycol of about 5000 D was activated with cyanuric chloride, and the activated compound was complexed to each of three proteins. Polyethylene glycol-superoxide dismutase and polyethylene glycol-catalase were each radioprotectants when administered prophylactically to female B6CBF1 mice before irradiation. The dose reduction factor for these mice was 1.2 when 5000 units of polyethylene glycol-catalase was administered before /sup 60/Co irradiation. Female B6CBF1 mice administered prophylactic intravenous injections of catalase, polyethylene glycol-albumin, or heat-denatured polyethylene glycol-catalase had survival rates similar to phosphate-buffered saline-injected control mice following /sup 60/Co irradiation. Polyethylene glycol-superoxide dismutase and polyethylene glycol-catalase have radioprotective activity in B6CBF1 mice, which appears to depend in part on enzymatic activities of the complex. However, no radioprotective effect was observed in male C57BL/6 mice injected with each polyethylene glycol-protein complex at either 3 or 24 hr before irradiation. The mechanism for radioprotection by these complexes may depend in part on other factors.

  4. Chemical interaction of polyethylene matrix with vegetable fillers in biocomposites

    NASA Astrophysics Data System (ADS)

    Pantyukhov, Petr; Monakhova, Tatiana; Popov, Anatoly; Zykova, Anna

    2016-05-01

    The paper studies the diffusion of low molecular weight components from vegetable fillers into polyethylene matrix during the preparation of biocomposites. In order to identify the diffusible substances a model experiment used where the hexadecane acted as a model of polyethylene. It was determined that polyphenolic compounds and chlorophyll penetrate from vegetable fillers to hexadecane to the maximum extent. There was found a correlation between the amount of polyphenolic compounds diffusible from the fillers to hexadecane and thermal oxidation kinetics of real biocomposites based on polyethylene and vegetable fillers. Thus, it has been assumed the diffusion of polyphenols and chlorophyll from vegetable fillers into polyethylene matrix during the preparation of biocomposites.

  5. Comparison of cross-linked polyethylene materials for orthopaedic applications.

    PubMed

    Collier, John P; Currier, Barbara H; Kennedy, Francis E; Currier, John H; Timmins, Graham S; Jackson, Simon K; Brewer, Robin L

    2003-09-01

    Cross-linked polyethylenes are being marketed by orthopaedic manufacturers to address the problem of osteolysis caused by polyethylene particulate wear debris. Wear testing of these cross-linked polyethylenes in hip simulators has shown dramatic reduction in wear rate compared with standard ultrahigh molecular weight polyethylene, either gamma irradiated in air or nitrogen - or ethylene oxide-sterilized. However, this reduction in wear rate is not without cost. The cross-linking processes can result in materials with lower mechanical properties than standard ultrahigh molecular weight polyethylene. To evaluate the effect of the various cross-linking processes on physical and mechanical properties of ultrahigh molecular weight polyethylene, commercially available cross-linked polyethylenes from six orthopaedic manufacturers were tested. This study was the culmination of collaboration with these manufacturers, who provided cross-linked polyethylene for this study, wear characteristics of the material they provided, and review of the physical and mechanical properties measure for their polyethylene. Cross-linked materials were evaluated as received and after an accelerated aging protocol. Free radical identity and concentration, oxidation, crystallinity, melt temperature, ultimate tensile strength, elongation at break, tensile stress at yield, and toughness are reported for each material. By comparing these physical and mechanical properties, surgeons can evaluate the trade-off that results from developing materials with substantially lower wear rates. PMID:12966304

  6. Anaerobic degradation of purified terephthalic acid wastewater using a novel, rapid mass-transfer circulating fluidized bed.

    PubMed

    Feng, Yangyang; Lu, Beibei; Jiang, Yu; Chen, Yinwen; Shen, Shubao

    2012-01-01

    The anaerobic treatability of purified terephthalic acid (PTA) wastewater in a novel, rapid mass-transfer fluidized bed reactor using brick particles as porous carrier materials was investigated. The reactor operation was stable after a short 34 day start-up period, with chemical oxygen demand (COD) removal efficiency between 65 and 75%, terephthalate (TA) removal efficiency between 60% and 70%, and system organic loading rate (OLR) increasing from 7.37 to 18.52 kg COD/m(3) d. The results demonstrate that the reactor is very efficient, and requires a low hydraulic retention time (HRT) of 8 h to remove both TA and COD from the high-concentration PTA wastewater. The system also has high resistance capacity to varied OLR. PMID:22592469

  7. Patterned functional carbon fibers from polyethylene

    SciTech Connect

    Hunt, Marcus A; Saito, Tomonori; Brown, Rebecca H; Kumbhar, Amar S; Naskar, Amit K

    2012-01-01

    Patterned, continuous carbon fibers with controlled surface geometry were produced from a novel melt-processible carbon precursor. This portends the use of a unique technique to produce such technologically innovative fibers in large volume for important applications. The novelties of this technique include ease of designing and fabricating fibers with customized surface contour, the ability to manipulate filament diameter from submicron scale to a couple of orders of magnitude larger scale, and the amenable porosity gradient across the carbon wall by diffusion controlled functionalization of precursor. The geometry of fiber cross-section was tailored by using bicomponent melt-spinning with shaped dies and controlling the melt-processing of the precursor polymer. Circular, trilobal, gear-shaped hollow fibers, and solid star-shaped carbon fibers of 0.5 - 20 um diameters, either in self-assembled bundle form, or non-bonded loose filament form, were produced by carbonizing functionalized-polyethylene fibers. Prior to carbonization, melt-spun fibers were converted to a char-forming mass by optimizing the sulfonation on polyethylene macromolecules. The fibers exhibited distinctly ordered carbon morphologies at the outside skin compared to the inner surface or fiber core. Such order in carbon microstructure can be further tuned by altering processing parameters. Partially sulfonated polyethylene-derived hollow carbon fibers exhibit 2-10 fold surface area (50-500 m2/g) compared to the solid fibers (10-25 m2/g) with pore sizes closer to the inside diameter of the filaments larger than the sizes on the outer layer. These specially functionalized carbon fibers hold promise for extraordinary performance improvements when used, for example, as composite reinforcements, catalyst support media, membranes for gas separation, CO2 sorbents, and active electrodes and current collectors for energy storage applications.

  8. Nonlinear viscoelastic characterization of thin polyethylene film

    NASA Technical Reports Server (NTRS)

    Wilbeck, J. S.

    1981-01-01

    In order to understand the state of stress and strain in a typical balloon fabricated from thin polyethylene film, experiment data in the literature reviewed. It was determined that the film behaves as a nonlinear viscoelasticity material and should be characterized accordingly. A simple uniaxial, nonlinear viscoelastic model was developed for predicting stress given a certain strain history. The simple model showed good qualitative agreement with results of constant rate, uniaxial accurately predicting stresses for cyclic strain histories typical of balloon flights. A program was outlined which will result in the development of a more complex nonlinear viscoelastic model.

  9. Biocompatible composites of ultrahigh molecular weight polyethylene

    NASA Astrophysics Data System (ADS)

    Panin, S. V.; Kornienko, L. A.; Suan, T. Nguen; Ivanova, L. P.; Korchagin, M. A.; Chaikina, M. V.; Shilko, S. V.; Pleskachevskiy, Yu. M.

    2015-10-01

    Mechanical and tribotechnical characteristics of biocompatible, antifriction and extrudable composites based on ultrahigh molecular weight polyethylene (UHMWPE) as well as hybrid matrix "UHMWPE + PTFE" with biocompatible hydroxyapatite filler under the dry friction and boundary lubrication were investigated. A comparative analysis of effectiveness of adding the hydroxyapatite to improve the wear resistance of composites based on these two matrices was performed. It is shown that the wear intensity of nanocomposites based on the hybrid matrix is lower than that for the composites based on pure UHMWPE. Possibilities of using the composites of the polymer "UHMWPE-PTFE" mixture as a material for artificial joints implants are discussed.

  10. Characterization of Polyethylene Glycol Modified Hemoglobins

    NASA Astrophysics Data System (ADS)

    Salazar, Gil; Barr, James; Morgan, Wayne; Ma, Li

    2011-03-01

    Polyethylene glycol modified hemoglobins (PEGHbs) was characterized by liquid chromatography and fluorescence methods. We prepared four samples of two different molecular weight PEG, 5KDa and 20KDa, modified bovine and human hemoglobin. We studied the oxygen affinities, stabilities, and peroxidase activities of PEGHbs. We have related oxygen affinities with different degrees of modifications. The data showed that the modification on the beta subunits was less stable than that of the alpha subunits on the human Hb based samples especially. We also compared peroxidase activities among different modified PEGHbs.

  11. Initial Stages of the Pyrolysis of Polyethylene.

    PubMed

    Popov, Konstantin V; Knyazev, Vadim D

    2015-12-10

    An experimental study of the kinetics of the initial stages of the pyrolysis of high-density polyethylene (PE) was performed. Quantitative yields of gas-phase products (C1-C8 alkanes and alkenes) and functional groups within the remaining polyethylene melt (methyl, vinyl, vinylene, vinylidene, and branching sites) were obtained as a function of time (0-20 min) at five temperatures in the 400-440 °C range. Gas chromatography and NMR ((1)H and (13)C) were used to detect the gas- and condensed-phase products, respectively. Modeling of polyethylene pyrolysis was performed, with the primary purpose of determining the rate constants of several critical reaction types important at the initial pyrolysis stages. Detailed chemical mechanisms were created (short and extended mechanisms) and used with both the steady-state approximation and numerical integration of the differential kinetic equations. Rate constants of critical elementary reactions (C-C backbone scission, two kinds of H-atom transfer, radical addition to the double bond, and beta-scission of tertiary alkyl radicals) were adjusted, resulting in an agreement between the model and the experiment. The values of adjusted rate constants are in general agreement with those of cognate reactions of small molecules in the gas phase, with the exception of the rate constants of the backbone C-C scission, which is found to be approximately 1-2 orders of magnitude lower. This observation provides tentative support to the hypothesis that congested PE melt molecular environment impedes the tumbling motions of separating fragments in C-C bond scission, thus resulting in less "loose" transition state and lower rate constant values. Sensitivity of the calculations to selected uncertainties in model properties was studied. Values and estimated uncertainties of four combinations of rate constants are reported as derived from the experimental results via modeling. The dependence of the diffusion-limited rate constant for radical

  12. Polyethelene terephthalate (PET) scrap recycling. (Latest citations from the Rubber and Plastics Research Association database). Published Search

    SciTech Connect

    Not Available

    1994-07-01

    The bibliography contains citations concerning the recycling of polyethelene terephthalate (PET) products. Discarded bottles and household PET scrap are primary sources of this material. Recycling machinery, processes, and programs are discussed. Cable insulation, sheet films, foam products, and other products made from recycled PET are described. The impact of recycling on resource conservation and waste disposal problems is evaluated. (Contains a minimum of 73 citations and includes a subject term index and title list.)

  13. Thermoluminescence Measurements of Medical Grade Polyethylene

    NASA Astrophysics Data System (ADS)

    Lewis, Scott; Dunlap, Greg; Palmer, Jeane; Jahan, M. S.

    1999-11-01

    Ultra-high molecular weight polyethylene (UHMWPE) is a biomaterial used in hip and knee joint replacements. Because this material is implanted into the body the material must be sterilized to prevent infection after implantation. Gamma irradiation is the most common method of sterilization, but it has one drawback; it causes the formation of free radicals and subsequent oxidative degradation of PE. By using thermoluminescence (TL) technique, free radical quenching temperature can be determined. In this study, UHMWPE was X-irradiated ( ~1 MRad at 10 keV) at 32 ^oC and subsequently heated to 200 ^oC at 1 ^oC / sec. The resulting luminescence known as thermoluminescence (TL) was recorded using a commercial TL dosimeter. The TL output, known as a glow curve, consists of two glow peaks, the prominent one occurs at 70 ^oC and a second one at 120 ^oC. It is suggested that the peak at 70 ^oC results from the recombination of free radicals due to molecular motion in the amorphous region, and the 120 ^oC peak is due to the motion of crystalline medium of the polyethylene matrix. Thermal annealing of free radicals as detected by TL can be a useful technique for diagnostic test of stabilization of radiation-sterilized medical joint components. *Supported by NSF REU Program (grant number EEC9619821) at the University of Memphis.

  14. Degradation of Green Polyethylene by Pleurotus ostreatus

    PubMed Central

    da Luz, José Maria Rodrigues; Paes, Sirlaine Albino; Ribeiro, Karla Veloso Gonçalves; Mendes, Igor Rodrigues; Kasuya, Maria Catarina Megumi

    2015-01-01

    We studied the biodegradation of green polyethylene (GP) by Pleurotus ostreatus. The GP was developed from renewable raw materials to help to reduce the emissions of greenhouse gases. However, little information regarding the biodegradation of GP discarded in the environment is available. P. ostreatus is a lignocellulolytic fungus that has been used in bioremediation processes for agroindustrial residues, pollutants, and recalcitrant compounds. Recently, we showed the potential of this fungus to degrade oxo-biodegradable polyethylene. GP plastic bags were exposed to sunlight for up to 120 days to induce the initial photodegradation of the polymers. After this period, no cracks, pits, or new functional groups in the structure of GP were observed. Fragments of these bags were used as the substrate for the growth of P. ostreatus. After 30 d of incubation, physical and chemical alterations in the structure of GP were observed. We conclude that the exposure of GP to sunlight and its subsequent incubation in the presence of P. ostreatus can decrease the half-life of GP and facilitate the mineralization of these polymers. PMID:26076188

  15. Polyethylene nanofibres with very high thermal conductivities.

    PubMed

    Shen, Sheng; Henry, Asegun; Tong, Jonathan; Zheng, Ruiting; Chen, Gang

    2010-04-01

    Bulk polymers are generally regarded as thermal insulators, and typically have thermal conductivities on the order of 0.1 W m(-1) K(-1). However, recent work suggests that individual chains of polyethylene--the simplest and most widely used polymer--can have extremely high thermal conductivity. Practical applications of these polymers may also require that the individual chains form fibres or films. Here, we report the fabrication of high-quality ultra-drawn polyethylene nanofibres with diameters of 50-500 nm and lengths up to tens of millimetres. The thermal conductivity of the nanofibres was found to be as high as approximately 104 W m(-1) K(-1), which is larger than the conductivities of about half of the pure metals. The high thermal conductivity is attributed to the restructuring of the polymer chains by stretching, which improves the fibre quality toward an 'ideal' single crystalline fibre. Such thermally conductive polymers are potentially useful as heat spreaders and could supplement conventional metallic heat-transfer materials, which are used in applications such as solar hot-water collectors, heat exchangers and electronic packaging. PMID:20208547

  16. Polyethylene wear in uncemented acetabular components.

    PubMed

    Hernandez, J R; Keating, E M; Faris, P M; Meding, J B; Ritter, M A

    1994-03-01

    We measured polyethylene wear in 231 porous-coated uncemented acetabular cups. We divided the hips into two groups according to the fixation of the femoral component, by cementing (n = 97) or press-fit (n = 134). Follow-up was from three to five years. The patients in two sub-groups were matched for weight, diagnosis, sex, age and length of follow-up. The linear wear rate of cups articulated with uncemented femoral components (0.22 mm/year) was significantly higher than the wear rate (0.15 mm/year) of cups articulated within cemented femoral components (p < 0.05). These results can be compared with previously reported wear rates of 0.08 mm/year for cemented all-polyethylene cups and 0.11 mm/year for cemented metal-backed cups. The higher wear rates of uncemented arthroplasties could jeopardize the long-term results of this type of hip replacement. PMID:8113288

  17. Nanostructurization and thermal properties of polyethylenes' welds

    NASA Astrophysics Data System (ADS)

    Galchun, Anatoliy; Korab, Nikolay; Kondratenko, Volodymyr; Demchenko, Valeriy; Shadrin, Andriy; Anistratenko, Vitaliy; Iurzhenko, Maksym

    2015-03-01

    As it is known, polyethylene (PE) is one of the common materials in the modern world, and PE products take the major share on industrial and trade markets. For example, various types of technical PE like PE-63, PE-80, and PE-100 have wide industrial applications, i.e., in construction, for pipeline systems etc. A rapid development of plastics industry outstrips detailed investigation of welding processes and welds' formation mechanism, so they remain unexplored. There is still no final answer to the question how weld's microstructure forms. Such conditions limit our way to the understanding of the problem and, respectively, prevent scientific approaches to the welding of more complicated (from chemical point of view) types of polymers than PE. Taking into account state-of-the-art, the article presents results of complex studies of PE weld, its structure, thermophysical and operational characteristics, analysis of these results, and basing on that some hypotheses of welded joint and weld structure formation. It is shown that welding of dissimilar types of polyethylene, like PE-80 and PE-100, leads to the formation of better-ordered crystallites, restructuring the crystalline phase, and amorphous areas with internal stresses in the welding zone.

  18. Degradation of Green Polyethylene by Pleurotus ostreatus.

    PubMed

    da Luz, José Maria Rodrigues; Paes, Sirlaine Albino; Ribeiro, Karla Veloso Gonçalves; Mendes, Igor Rodrigues; Kasuya, Maria Catarina Megumi

    2015-01-01

    We studied the biodegradation of green polyethylene (GP) by Pleurotus ostreatus. The GP was developed from renewable raw materials to help to reduce the emissions of greenhouse gases. However, little information regarding the biodegradation of GP discarded in the environment is available. P. ostreatus is a lignocellulolytic fungus that has been used in bioremediation processes for agroindustrial residues, pollutants, and recalcitrant compounds. Recently, we showed the potential of this fungus to degrade oxo-biodegradable polyethylene. GP plastic bags were exposed to sunlight for up to 120 days to induce the initial photodegradation of the polymers. After this period, no cracks, pits, or new functional groups in the structure of GP were observed. Fragments of these bags were used as the substrate for the growth of P. ostreatus. After 30 d of incubation, physical and chemical alterations in the structure of GP were observed. We conclude that the exposure of GP to sunlight and its subsequent incubation in the presence of P. ostreatus can decrease the half-life of GP and facilitate the mineralization of these polymers. PMID:26076188

  19. SECURING CONTAINERIZED HAZARDOUS WASTES WITH POLYETHYLENE RESIN AND FIBERGLASS ENCAPSULATES

    EPA Science Inventory

    This study investigates the fabrication and use of polyethylene resin and fiberglass to encapsulate and secure containerized hazardous wastes. Laboratory-scale encapsulates of composite structure were made from powdered, high-density polyethylene (HDPE) and epoxy-resin-wetted fib...

  20. 21 CFR 177.1630 - Polyethylene phthalate polymers.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene phthalate polymers. 177.1630 Section... (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as... polymers. Polyethylene phthalate polymers identified in this section may be safely used as, or...