Science.gov

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

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-15

    ... From the Federal Register Online via the Government Publishing Office ] INTERNATIONAL TRADE COMMISSION Polyethylene Terephthalate (Pet) Film From Korea AGENCY: United States International Trade... full five-year review concerning the antidumping duty order on polyethylene terephthalate (PET)...

  4. 76 FR 54791 - Polyethylene Terephthalate (PET) Film From Korea

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-02

    ... COMMISSION Polyethylene Terephthalate (PET) Film From Korea Determination On the basis of the record \\1... antidumping duty order on polyethylene terephthalate (PET) film from Korea would not be likely to lead to... contained in USITC Publication 4254 (August 2011), entitled Polyethylene Terephthalate (PET) Film from...

  5. Powder Production From Waste Polyethylene Terephthalate (PET) Water Bottles

    DTIC Science & Technology

    2014-06-01

    Powder Production From Waste Polyethylene Terephthalate (PET) Water Bottles by Anit Giri, Frank Kellogg, Kyu Cho, and Marc Pepi ARL-MR...871 June 2014 Powder Production From Waste Polyethylene Terephthalate (PET) Water Bottles Anit Giri and Frank Kellogg Bowhead Science and...Polyethylene Terephthalate (PET) Water Bottles 5a. CONTRACT NUMBER 5b. GRANT NUMBER 5c. PROGRAM ELEMENT NUMBER 6. AUTHOR(S) Anit Giri, * Frank

  6. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Partial... request an administrative review of the antidumping duty (AD) order on polyethylene terephthalate film... Polyester Film, Inc., SKC, Inc., and Toray Plastics (America), Inc. \\3\\ See Polyethylene Terephthalate...

  7. 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...

  8. 78 FR 48147 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-07

    ...] Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Countervailing Duty... the countervailing duty (CVD) order on polyethylene terephthalate film, sheet and strip (PET film..., the products covered are all gauges of raw, pretreated, or primed polyethylene terephthalate...

  9. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results... polyethylene terephthalate film (PET Film) from Taiwan.\\1\\ This review covers two respondents, Shinkong.... \\1\\ See Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary Results...

  10. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary... semiannual new shipper review (NSR) under the antidumping duty order on polyethylene terephthalate film... Fair Value and Antidumping Duty Order: Polyethylene Terephthalate Film, Sheet, and Strip from India,...

  11. 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...

  12. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip from India: Preliminary... polyethylene terephthalate film, sheet and strip from India covering the period January 1, 2010, through... Vacmet and Polypacks. See Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission,...

  13. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan; Preliminary... conducting an administrative review of the antidumping duty order on polyethylene terephthalate film, sheet... preliminary results. \\1\\ See Polyethylene Terephthalate Film, Sheet and Strip from Taiwan: Partial...

  14. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic... the antidumping duty order on polyethylene terephthalate film, sheet, and strip (``PET film'') from... Duty Administrative Review: Polyethylene Terephthalate Film, Sheet, and Strip from the...

  15. 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...

  16. 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...

  17. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab...) is conducting an administrative review of the antidumping duty order on polyethylene terephthalate... from the UAE. See Polyethylene Terephthalate Film, Sheet, and Strip From Brazil, the People's...

  18. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results...) issued the preliminary results of the administrative review of polyethylene terephthalate film, sheet and... Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Countervailing...

  19. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission of... an administrative review of the countervailing duty (CVD) order on polyethylene terephthalate film... administrative review with respect to Vacmet and Polypacks. See Polyethylene Terephthalate Film, Sheet and...

  20. 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...

  1. 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.

  2. 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.

  3. 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.

  4. Acetone transport in poly(ethylene terephthalate)

    NASA Astrophysics Data System (ADS)

    Ouyang, Hao; Chen, Che-Chen

    1997-05-01

    Organic solvents like acetone can penetrate into poly(ethylene terephthalate) (PET). The model of case I (Fickian) and case II (swelling) is employed to study the phenomenon of mass transport. This model is successful in explaining the behavior of mass transport in an amorphous polymer, for example, poly(methyl methacrylate) (PMMA). The characteristic parameters, diffusivity D and velocity v, can be obtained from the analysis of experimental data. The mass transport in PET is different from that in PMMA. It is accompanied by a large-scale structural rearrangement, which leads to induced crystallization of the original amorphous state. This is the so-called "solvent-induced crystallization." Acetone-induced crystallization was confirmed by x-ray diffraction. The differential scanning calorimetry thermograms of acetone-treated PET show that the crystallization peak disappears and the glass transition temperature decreases.

  5. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab... (the Department) is conducting an administrative review of the antidumping duty order on polyethylene...- treated, or primed polyethylene terephthalate film, whether extruded or co-extruded. Excluded...

  6. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip from India: Final Results... the preliminary results of administrative review of the countervailing duty order on polyethylene..., 2007. See Polyethylene Terephthalate Film, Sheet, and Strip from India: Preliminary Results...

  7. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From Brazil: Preliminary... Commerce (the Department) initiated an administrative review of the antidumping duty order on polyethylene... Preliminary Results of the Antidumping Duty Administrative Review of Polyethylene Terephthalate Film,...

  8. Polyethylene terephthalate degradation under reactor neutron irradiation

    NASA Astrophysics Data System (ADS)

    Chikaoui, K.; Izerrouken, M.; Djebara, M.; Abdesselam, M.

    2017-01-01

    This paper is devoted to study the defects generated by reactor neutron in polyethylene terephthalate (PET) films. The explored fast neutron fluence ranges from 2.02×1016 to 2.07×1018 n cm-2. The induced damages were investigated using ultraviolet-visible spectrophotometry (UV-vis), Fourier Transform Infrared spectrometry (FTIR) and X-ray diffraction (XRD). The UV-vis spectra show important changes indicating the degradation of the chemical structure and the creation of new chromophores. FTIR spectra reveal that the intensities of the different absorption bands decrease linearly under fast neutron irradiation. The internal reference band at 1410 cm-1 is used to follow the overall damage during irradiation. The 1342 cm-1 band corresponding to CH2 wagging of trans conformation of crystalline phase show a sharpe linear decrease as the fast neutrons fluence goes up. The creation of the monosubstituted benzene, investigated using the 1610 cm-1 band. It shows a linear increase with fast neutron fluence. It is found from XRD analysis that the diffraction peak (100) intensity is drastically reduced after irradiation at 2.02×1016 n cm-2.

  9. 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

    ... From the Federal Register Online via the Government Publishing Office ] DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet and strip...

  10. 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

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in... administrative review of the countervailing duty order on polyethylene terephthalate film, sheet and strip...

  11. 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

    ... From the Federal Register Online via the Government Publishing Office ] DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, In... (CVD) order on polyethylene terephthalate film, sheet and strip from India covering the period...

  12. 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

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Partial... (CVD) order on polyethylene terephthalate film, sheet and strip from India covering the period...

  13. 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

    ... International Trade Administration Polyethylene Terephthalate (PET) Film, Sheet, and Strip From India: Final... of the countervailing duty order on polyethylene terephthalate (PET) film, sheet, and strip (``PET film'') from India. The Department finds that revocation of this countervailing duty order...

  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

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... polyethylene terephthalate film, sheet and strip from India covering the period January 1, 2009,...

  15. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET... Determination of Sales at Less Than Fair Value and Antidumping Duty Order: Polyethylene Terephthalate...

  16. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet and strip (PET Film... are listed in the ``Final Results of Review'' section, below. \\1\\ See Polyethylene Terephthalate...

  17. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results... order on polyethylene terephthalate film (PET Film) from India.\\1\\ This review covers three respondents... the ``Final Results of Review'' section below. \\1\\ See Polyethylene Terephthalate Film, Sheet,...

  18. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Final Results...) published the preliminary results of administrative review of the antidumping duty order on polyethylene terephthalate film (PET Film) from Taiwan. See Polyethylene Terephthalate Film, Sheet, and Strip From...

  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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab...) is conducting an administrative review of the antidumping duty order on polyethylene terephthalate... on PET Film from the UAE. See Polyethylene Terephthalate Film, Sheet, and Strip From Brazil,...

  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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip from India: Initiation of...) orders on Polyethylene Terephthalate Film, Sheet and Strip (PET Film) from India. The Department... Less Than Fair Value and Antidumping Duty Order: Polyethylene Terephthalate Film, Sheet, and Strip...

  1. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Preliminary... ] administrative review of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET...: Polyethylene Terephthalate Film, Sheet, and Strip (PET Film) from Taiwan, 67 FR 46566 (July 1, 2002). On July...

  2. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET... Determination of Sales at Less Than Fair Value and Antidumping Duty Order: Polyethylene Terephthalate...

  3. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab... antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET Film) from the United Arab... primed polyethylene terephthalate film, whether extruded or co-extruded. Excluded are metallized...

  4. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results...) issued the preliminary results of the new shipper review of polyethylene terephthalate film, sheet and... INFORMATION: Background Since the issuance of Polyethylene Terephthalate Film, Sheet, and Strip From...

  5. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Final Results...) issued the preliminary results of the new shipper review of polyethylene terephthalate film, sheet and... Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Countervailing Duty...

  6. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... the antidumping duty order on polyethylene terephthalate film, sheet and strip from India for the period July 1, 2009 through December 31, 2009. See Polyethylene Terephthalate Film, Sheet and Strip...

  7. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of...) order on polyethylene terephthalate film, sheet and strip from India covering the period July 1, 2010... respect to Vacmet and Polypacks on September 20, 2011. See Polyethylene Terephthalate Film, Sheet...

  8. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Korea: Notice of... polyethylene terephthalate film, sheet, ] and strip from Korea on July 28, 2011.\\1\\ This review covers one... the antidumping duty order on polyethylene terephthalate film, sheet, and strip from Korea with...

  9. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India and Taiwan...'') initiated the second sunset review of the antidumping duty orders on Polyethylene Terephthalate Film, Sheet... Value and Antidumping Duty Order: Polyethylene Terephthalate Film, Sheet, and Strip from India, 67...

  10. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Preliminary... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET... Department published the antidumping duty order on PET film from Brazil. See Polyethylene Terephthalate...

  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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea... its third sunset review of the antidumping duty order on polyethylene terephthalate film, sheet, and... existing antidumping duty order on polyethylene terephthalate film, sheet, and strip from the Republic...

  12. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in... administrative review of the antidumping duty (AD) order on polyethylene terephthalate film, sheet and strip from... respect to Vacmet and Polypacks on September 20, 2011. See Polyethylene Terephthalate Film, Sheet...

  13. 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

    ... 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 film.... SUPPLEMENTARY INFORMATION: Background The antidumping duty order on polyethylene terephthalate film, sheet,...

  14. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic... review of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (``PET film... review (``POR'') is November 1, 2010, through October 31, 2011. \\1\\ See Polyethylene Terephthalate...

  15. 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... Devices § 878.5000 Nonabsorbable poly(ethylene terephthalate) surgical suture. (a) Identification. Nonabsorbable poly(ethylene terephthalate) surgical suture is a multifilament, nonabsorbable, sterile,...

  16. 75 FR 53711 - Polyethylene Terephthalate (PET) Film From Korea

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-01

    ... [Federal Register Volume 75, Number 169 (Wednesday, September 1, 2010)] [Notices] [Pages 53711-53714] [FR Doc No: 2010-21366] INTERNATIONAL TRADE COMMISSION [Investigation No. 731-TA-459 (Third Review)] Polyethylene Terephthalate (PET) Film From Korea AGENCY: United States International...

  17. Laser transmission welding of poly(ethylene terephthalate) and biodegradable poly(ethylene terephthalate) - Based blends

    NASA Astrophysics Data System (ADS)

    Gisario, Annamaria; Veniali, Francesco; Barletta, Massimiliano; Tagliaferri, Vincenzo; Vesco, Silvia

    2017-03-01

    Joining of Poly(Ethylene Terephthalate) PET and its biodegradable derivatives is of high relevance to ensure good productive rate, low cost and operational safety for fabrication of medical and electronic devices, sport equipments as well as for manufacturing of food and drug packaging solutions. In the present investigation, granules of PET and PETs modified by organic additives, which promote biodegradation of the polymeric chains, were prepared by extrusion compounding. The achieved granules were subsequently re-extruded to shape thin (330 μm) flat sheets. Substrates cut from these sheets were joined by Laser Transmission Welding (LTW) with a continuous wave High Power Diode Laser (cw-HPDL). First, based on a qualitative evaluation of the welded joints, the most suitable operational windows for PETs laser joining were identified. Second, characterization of the mechanical properties of the welded joints was performed by tensile tests. Accordingly, Young's modulus of PET and biodegradable PET blends was studied by Takayanagi's model and, based on the experimental results, a novel predicting analytical model derived from the mixture rule was developed. Lastly, material degradation of the polymeric joints was evaluated by FT-IR analysis, thus allowing to identify the main routes to thermal degradation of PET and, especially, of biodegradable PET blends during laser processing.

  18. 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

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

  19. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... 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 Duty and...

  20. 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.

  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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in... administrative review of the countervailing duty (CVD) order on polyethylene terephthalate film, sheet and strip... administrative review with respect to Vacmet and Polypacks on September 20, 2011. See Polyethylene...

  2. Manufacturing, structure and properties of recycled polyethylene terephthalate /liquid crystal polymer/montmorillonite clay nanocomposites

    NASA Astrophysics Data System (ADS)

    Japins, Guntis; Berzina, Rita; Zicans, Janis; Merijs Meri, Remo; Ivanova, Tatjana; Kalkis, Valdis; Reinholds, Ingars

    2013-12-01

    Polyethylene terephthalate (PET)/liquid crystal polymer (LCP)/monthmorillonite clay (MMT) compositions were obtained by melt mixing. Their mechanical, structural, rheological and thermal properties were investigated.

  3. 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.

  4. 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

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE 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...

  5. 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.

  6. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip from Taiwan: Extension of... polyethylene terephthalate film, sheet and strip from Taiwan for the period July 1, 2008 through June 30, 2009... time that the Department conducted an administrative review of the antidumping order on...

  7. 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

    ... From the Federal Register Online via the Government Publishing Office INTERNATIONAL TRADE 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...

  8. 76 FR 47558 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-05

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary... administrative review under the countervailing duty (CVD) order on polyethylene terephthalate film, sheet and... Register the CVD order on PET Film from India. See Notice of Countervailing Duty Order:...

  9. 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

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Notice of... polyethylene terephthalate film, sheet, and strip (PET Film) from Brazil for the period November 1,...

  10. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Korea: Final Results... of the antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET film) from Korea, covering the June 1, 2009, to May 31, 2010, period of review (POR).\\1\\ \\1\\ See...

  11. 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

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Rescission, in...) order on polyethylene terephthalate film, sheet and strip from India covering the period July 1,...

  12. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic... of polyethylene terephthalate film, sheet, and strip (``PET film'') from the People's Republic of... notice of initiation of the second administrative review of the antidumping duty order on PET film...

  13. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the People's Republic... review of polyethylene terephthalate film, sheet, and strip (``PET film'') from the People's Republic of... notice of initiation of the second administrative review of the antidumping duty order on PET film...

  14. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip from the Republic of Korea... administrative review of the antidumping duty order on polyethylene terephthalate film, sheet and strip (PET film... the antidumping duty order on PET film from Korea. See Antidumping or Countervailing Duty...

  15. Qualitative comparison of polyethylene terephthalate flakes from various collection systems in Germany.

    PubMed

    Snell, H; Nassour, A; Nelles, M

    2017-02-01

    In 2003, a deposit system for one-way packaging was introduced in Germany. Since that time, polyethylene terephthalate beverage packaging is collected through various collection systems, a deposit system, a reusable packaging system and the 'Green Dot' (the dual system) with the yellow bag. The manner of collection had a decisive influence on the quality of the generated recycled materials. The research at hand shows for the first time how the quality of polyethylene terephthalate flakes depends on the type of collection system. The results are based on a 14-year time frame, during which the quality of the polyethylene terephthalate flakes was examined using the different collection systems. The criterion used was the amount of contamination of polyethylene terephthalate flakes with various polymers, metals and other substances. Grain size and bulk density were also compared. The outcome shows that material from the deposit systems resulted in a better quality of polyethylene terephthalate (PET) flakes.

  16. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea... polyethylene terephthalate film, sheet and strip (PET film) from the Republic of Korea (Korea). See Polyethylene Terephthalate Film, Sheet, and Strip from the Republic of Korea: Preliminary Results...

  17. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab... duty order on polyethylene terephthalate film (PET Film) from the United Arab Emirates.\\1\\ This review... ``Final Results of Review.'' \\1\\ See Polyethylene Terephthalate Film, Sheet, and Strip from the...

  18. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab... duty order on polyethylene terephthalate film (PET Film) from the United Arab Emirates. This review... preliminary results, the following events have taken place. See Polyethylene Terephthalate Film, Sheet,...

  19. Electron beam induced modification of poly(ethylene terephthalate) films

    NASA Astrophysics Data System (ADS)

    Vasiljeva, I. V.; Mjakin, S. V.; Makarov, A. V.; Krasovsky, A. N.; Varlamov, A. V.

    2006-10-01

    Electron beam processing of poly(ethylene terephthalate) (PET) films is found to promote significant changes in the melting heat, intrinsic viscosity and polymer film-liquid (water, isooctane and toluene) boundary surface tension. These properties are featured with several maximums depending on the absorbed dose and correlating with the modification of PET surface functionality. Studies using adsorption of acid-base indicators and IR-spectroscopy revealed that the increase of PET surface hydrophilicity is determined by the oxidation of methylene and methyne groups. Electron beam treatment of PET films on the surface of N-vinylpyrrolidone aqueous solution provided graft copolymerization with this comonomer at optimum process parameters (energy 700 keV, current 1 mA, absorbed dose 50 kGy).

  20. CO2 laser ablative etching of polyethylene terephthalate

    NASA Astrophysics Data System (ADS)

    Dyer, P. E.; Oldershaw, G. A.; Sidhu, J.

    1989-06-01

    Films of polyethylene terephthalate (PET) can be successfully etched with 9 μm radiation from a pulsed TEA CO2 laser. The relationship between etch depth and fluence is broadly similar to that observed for excimer laser etching but with a less well-defined threshold. Time-resolved photoacoustic measurements of stress waves generated in the interaction show that at a fluence of 1.8 J cm-2 ablation occurs 100 200 ns after the start of the laser pulse, a time which is consistent with the rate of thermal decomposition of PET. The volatile products of ablation are carbon monoxide, carbon dioxide, methane, ethyne, ethene, benzene, ethanal, and small quantities of other products. For fluences close to and appreciably above the threshold the ablated material consists predominantly of involatile species of relatively high molecular weight, whereas at higher fluences substantial fragmentation of the polymer to small molecules occurs.

  1. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... under the countervailing duty order on polyethylene terephthalate film, sheet and strip from India for... Terephthalate Film, Sheet, and Strip From India: Preliminary Results of Countervailing Duty New Shipper...

  2. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Final Results...) published the preliminary results of the administrative review of the antidumping duty order on polyethylene... covering PET film from Brazil and invited interested parties to comment. See Polyethylene...

  3. 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

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... terephthalate film, sheet and strip from India covering the period July 1, 2009, through June 30, 2010....

  4. Novel beta-emitting poly(ethylene terephthalate) surface modification.

    PubMed

    Qu, X; Weinberger, J

    2000-12-05

    Restenosis after percutaneous interventions in coronary and peripheral arteries leads to repeat procedures and surgery in a significant number of patients. We have previously demonstrated that irradiation of an arterial site using an endovascular source (brachytherapy) is highly effective in preventing the restenotic process. To this end, a novel beta radiation delivery system was developed, based on the adsorption of (32)P (o-phosphoric acid) by pH-sensitive chitosan hydrogel on a poly(ethylene terephthalate) (PET) balloon surface. The PET balloon surface was treated with oxygen plasma and coated with chitosan hydrogel. Covalent bonds, ionic bonds, and hydrogen bonds all contribute to the adhesion between chitosan hydrogel and PET. In the aqueous phosphoric acid (PA) solution, the -NH(2) groups of chitosan were protonated by PA and the adsorption of PA occurred at the same time. The effect of PA concentration and temperature on adsorption efficiency and kinetics were studied. More than 70% PA was adsorbed on the sample surface in 0.2 mM PA solution. The surface of samples was also investigated by attenuated total reflection-Fourier transform infrared spectroscopy and scanning electron microscopy. PET surface may be modified to carry high activity beta emitters; such materials may be useful in a therapeutic setting

  5. Surface modification on polyethylene terephthalate films with 2-methacryloyloxyethyl phosphorylcholine.

    PubMed

    Zheng, Zhiwen; Ren, Li; Zhai, Zhichen; Wang, Yingjun; Hang, Fei

    2013-07-01

    In this study, the surface of polyethylene terephthalate (PET) was modified to improve the protein and cell adhesion behavior with low temperature ammonia plasma treatment followed by 2-methacryloyloxyethyl phosphorylcholine (MPC) grafting. The x-ray photoelectron spectroscopy (XPS) results showed that the -COO(-), -N-C=O and -P-O-H groups were successfully incorporated onto the sample surface after MPC grafting. Furthermore, formation of new bonds, -N= and N-H on the sample surface grafted with MPC was recorded by Fourier transform infrared spectroscopy (FTIR). A large number of spherical particles at submicron to nanometer scale were also observed on the surface by atomic force microscopy (AFM). The cell adhesion experiments on PET film surfaces were evaluated and the highly hydrophilic surfaces could not promote cell adhesion and spreading. All results achieved in this study have clearly indicated that the method combining low temperature ammonia plasma treatment and MPC grafting is an effective way of producing a suitably hydrophilic PET surface with the capability of weakening the protein adsorption greatly.

  6. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Brazil: Final Results...) published the preliminary results of the administrative review of the antidumping duty order on polyethylene... duty order covering PET film from Brazil and invited interested parties to comment. See...

  7. 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

    ... [Federal Register Volume 77, Number 249 (Friday, December 28, 2012)] [Notices] [Page 76456] [FR Doc No: 2012-31320] DEPARTMENT OF COMMERCE International Trade Administration [A-583-837] Polyethylene... an administrative review of the antidumping duty (AD) order on polyethylene terephthalate film,...

  8. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Amended Final... Department) published the final results of the antidumping duty administrative review of polyethylene...), pursuant to section 751(h) of the Tariff Act of 1930, as amended (the Act). \\1\\ See...

  9. 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

  10. 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

  11. Surface pre-treatment for barrier coatings on polyethylene terephthalate

    NASA Astrophysics Data System (ADS)

    Bahre, H.; Bahroun, K.; Behm, H.; Steves, S.; Awakowicz, P.; Böke, M.; Hopmann, Ch; Winter, J.

    2013-02-01

    Polymers have favourable properties such as light weight, flexibility and transparency. Consequently, this makes them suitable for food packaging, organic light-emitting diodes and flexible solar cells. Nonetheless, raw plastics do not possess sufficient barrier functionality against oxygen and water vapour, which is of paramount importance for most applications. A widespread solution is to deposit thin silicon oxide layers using plasma processes. However, silicon oxide layers do not always fulfil the requirements concerning adhesion and barrier performance when deposited on films. Thus, plasma pre-treatment is often necessary. To analyse the influence of a plasma-based pre-treatment on barrier performance, different plasma pre-treatments on three reactor setups were applied to a very smooth polyethylene terephthalate film before depositing a silicon oxide barrier layer. In this paper, the influence of oxygen and argon plasma pre-treatments towards the barrier performance is discussed examining the chemical and topological change of the film. It was observed that a short one-to-ten-second plasma treatment can reduce the oxygen transmission rate by a factor of five. The surface chemistry and the surface topography change significantly for these short treatment times, leading to an increased surface energy. The surface roughness rises slowly due to the development of small spots in the nanometre range. For very long treatment times, surface roughness of the order of the barrier layer's thickness results in a complete loss of barrier properties. During plasma pre-treatment, the trade-off between surface activation and roughening of the surface has to be carefully considered.

  12. 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.

  13. 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

    ... From the Federal Register Online via the Government Publishing Office INTERNATIONAL TRADE COMMISSION Polyethylene Terephthalate Film, Sheet, and Strip From India and Taiwan; Institution of Five-Year... polyethylene terephthalate film, sheet, and strip (``PET film'') from India and the antidumping duty orders...

  14. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From the United Arab... duty order on polyethylene terephthalate film (PET Film) from the United Arab Emirates.\\1\\ This review... final dumping margins, see the ``Final Results of Review'' section below. \\1\\ See...

  15. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of... under the antidumping duty order on polyethylene terephthalate film, sheet and strip from India for SRF... Film, Sheet and Strip from India: Preliminary Results of Antidumping Duty New Shipper Review, 75...

  16. 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

    ... International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip From Taiwan: Notice of... antidumping duty order on polyethylene terephthalate film, sheet, and strip (PET Film) from Taiwan.\\1\\ The... contained a clerical error, in that it identified an incorrect case number associated with PET Film...

  17. 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

  18. 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...

  19. 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...

  20. 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...

  1. 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...

  2. 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.

  3. 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…

  4. 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...

  5. 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...

  6. 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

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet and Strip From India: Extension of Time Limit for Preliminary Results of Countervailing Duty New Shipper Review AGENCY: Import Administration, International Trade...

  7. 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

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film from India and Taiwan: Extension of Time Limits for Preliminary and Final Results of the Second Antidumping Duty Sunset Reviews AGENCY: Import Administration, International...

  8. 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

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE International Trade Administration Polyethylene Terephthalate Film, Sheet, and Strip (PET Film) From Taiwan: Extension of Time Limit for the Preliminary Results of the Antidumping Duty Administrative Review...

  9. 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.

  10. Use of polyethylene terephthalate for temporal recompression of intense femtosecond laser pulses

    NASA Astrophysics Data System (ADS)

    Mironov, S. Yu; Ginzburg, V. N.; Gacheva, E. I.; Silin, D. E.; Kochetkov, A. A.; Mamaev, Yu A.; Shaykin, A. A.; Khazanov, E. A.; Mourou, G. A.

    2015-02-01

    The linear characteristics of polyethylene terephthalate, such as index of refraction, spectral transmittance and transverse distribution of phase and polarization distortions, have been measured. Spectrum broadening of laser pulses (intensity over 1.3 ТW cm-2) after propagation through a 0.7 mm thick sample has been demonstrated in experiment. Taking into consideration almost unlimited aperture, submillimeter thickness and the low cost of polyethylene terephthalate, the obtained results demonstrate that it is a prospective material to be used for spectrum broadening and subsequent time compression of petawatt laser pulses to single cycle regime (Mourou et al 2014 Single cycle thin film compressor opening the door to zeptosecond-exawatt physics Eur. Phys. J. Spec. Top. 223 1181-8).

  11. 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.

  12. Synthesis and characterization of azo acrylates grafted onto polyethylene terephthalate by gamma irradiation

    NASA Astrophysics Data System (ADS)

    Bucio, Emilio; Skewes, Phill; Burillo, Guillermina

    2005-07-01

    Polyethylene terephthalate (PET) films were grafted with acryloyl chloride by gamma irradiation, and the grafted films were reacted with Disperse Red 1 or 4-phenylazophenol. The films where characterized by atomic force microscopy, differential scanning calorimetry, FTIR-ATR, light polarized microscopy, elemental analysis and UV spectroscopy. The surface of the films was homogeneous, and the dye underwent trans to cis photoreaction, whereby the red films became colorless by the irradiation of UV light at room temperature.

  13. 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.

  14. Grafting onto poly(ethylene terephthalate) driven by 172 nm UV light

    NASA Astrophysics Data System (ADS)

    Zhu, Zhengmao; Kelley, Michael J.

    2005-10-01

    The reactivity of the surface of poly(ethylene terephthalate) (PET) film under 172 nm UV irradiation (xenon excimer lamp) towards nitrogen-borne 1-octene, n-nonane and heptafluorodecene vapor was investigated. Materials receiving from 0 to 24 J/cm 2 of UV were examined by X-ray photoelectron spectroscopy (XPS), time of flight secondary ion mass spectroscopy (ToF/SIMS), water and mineral oil contact angle measurement and atomic force microscopy (AFM). A uniform nanoscale layer developed on PET surface attributed to the grafting reaction between photolytically-produced polymer radicals and vapor phase molecules.

  15. Determination of potential migrants from commercial amber polyethylene terephthalate bottle wall

    SciTech Connect

    Kim, H.; Gilbert, S.G.; Johnson, J.B. )

    1990-02-01

    Potential migrants were isolated from commercial polyethylene terephthalate (PET) bottles using Soxhlet extraction. The concentrated extract was then subjected to GC/MS analysis. A total of 19 migrants has been identified. The majority of compounds appeared to be intermediate reaction products or residual monomers of their dehydration and transesterification products. Several processing aids such as fatty acids and commonly used plasticizers were also identified. The amount of seven compounds present in the major portion of exhaustive extract of the PET bottle wall ranged from 800 micrograms/g polymer to as low as 0.6 microgram/g.

  16. 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.

  17. 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

    ... 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 Taiwan... it is not practicable to complete the preliminary results of the administrative review of PET...

  18. 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.

  19. Western blot membrane composed of electrospun polyvinylidene fluoride nanofiber membrane and polyethylene terephthalate sheet.

    PubMed

    Cho, Eugene; Kim, Chan; Hwang, Cheol Ho; Chang, Duck Rye; Kook, Joong-Ki

    2013-06-01

    In a previous study, an electrospun polyvinylidene fluoride (PVDF) nanofiber membrane was developed for Western blotting. The membrane exhibited high sensitivity and high binding capacity for the detection of protein bands that was unlike that observed for conventional, microphase separation-based porous PVDF membranes. Nevertheless, the PVDF nanofiber membrane is quite expensive. The objective of this study was to develop an economical Western blot membrane using a hybrid electrospun PVDF nanofiber and polyethylene terephthalate (PET) sheet. The results showed that the detection sensitivity of the 4 gram per square meter (gsm) membrane was similar to those of the electrospun PVDF nanofiber membrane only, and the 7 gsm PVDF nanofiber membranes on a PET sheet and the electrospun PVDF nanofiber membrane. This means the protein detection sensitivity is not proportional to the thickness of the PVDF nanofiber membrane. The 4 gsm PVDF nanofiber membrane on a PET sheet can be used to detect proteins with high sensitivity and economic efficiency.

  20. 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.

  1. 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.

  2. Effect of sterilization on non-woven polyethylene terephthalate fiber structures for vascular grafts.

    PubMed

    Dimitrievska, Sashka; Petit, Alain; Doillon, Charles J; Epure, Laura; Ajji, Abdellah; Yahia, L'Hocine; Bureau, Martin N

    2011-01-10

    Non-woven polyethylene terephthalate (PET) fibers produced via melt blowing and compounded into a 6 mm diameter 3D tubular scaffold were developed with artery matching mechanical properties. This work compares the effects of ethylene oxide (EtO) and low temperature plasma (LTP) sterilization on PET surface chemistry and biocompatibility. As seen through X-ray photoelectron spectroscopy (XPS) analysis, LTP sterilization led to an increase in overall oxygen content and the creation of new hydroxyl groups. EtO sterilization induced alkylation of the PET polymer. The in vitro cytotoxicity showed similar fibroblastic viability on LTP- and EtO-treated PET fibers. However, TNF-α release levels, indicative of macrophage activation, were significantly higher when macrophages were incubated on EtO-treated PET fibers. Subcutaneous mice implantation revealed an inflammatory response with foreign body reaction to PET grafts independent of the sterilization procedure.

  3. 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.

  4. Heating rate effect on char yield from cotton, poly(ethylene terephthalate) and blend fabrics.

    PubMed

    Alongi, Jenny; Camino, Giovanni; Malucelli, Giulio

    2013-02-15

    Thermal behaviour of polymers is generally assessed by relatively low heating rate, such as in thermogravimetry (typically at 10 °C/min), which leads to progressive decomposition of chemical bonds with increasing dissociation energy under thermodynamic control. However, polymer materials may be accidentally exposed to high heating rates such as in a fire, when their thermal decomposition, occurring through competing paths, becomes kinetically controlled and may lead to heating rate dependence of their degradation mechanisms and products. In the present paper, thermogravimetry at 100, 200 and 300 °C/min heating rates has been carried out on cotton, poly(ethylene terephthalate) and their blend fabrics, which decompose with partial charring. The obtained results show that the char, produced by thermal and thermo-oxidative degradation of such polymer materials, is affected by the heating rate essentially in terms of thermal stability and yield, depending on the type of polymer and the absence or presence of air oxygen.

  5. 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.

  6. Development of high shrinkage polyethylene terephthalate (PET) shape memory polymer tendons for concrete crack closure

    NASA Astrophysics Data System (ADS)

    Teall, Oliver; Pilegis, Martins; Sweeney, John; Gough, Tim; Thompson, Glen; Jefferson, Anthony; Lark, Robert; Gardner, Diane

    2017-04-01

    The shrinkage force exerted by restrained shape memory polymers (SMPs) can potentially be used to close cracks in structural concrete. This paper describes the physical processing and experimental work undertaken to develop high shrinkage die-drawn polyethylene terephthalate (PET) SMP tendons for use within a crack closure system. The extrusion and die-drawing procedure used to manufacture a series of PET tendon samples is described. The results from a set of restrained shrinkage tests, undertaken at differing activation temperatures, are also presented along with the mechanical properties of the most promising samples. The stress developed within the tendons is found to be related to the activation temperature, the cross-sectional area and to the draw rate used during manufacture. Comparisons with commercially-available PET strip samples used in previous research are made, demonstrating an increase in restrained shrinkage stress by a factor of two for manufactured PET filament samples.

  7. Material characterization and thermoforming of polyethylene terephthalate film for electrical insulation: Topical report

    SciTech Connect

    Carey, D.A.; Smith, B.P.

    1987-12-01

    Differential scanning calorimetry (DSC) was used to determine as-received glass transition, crystallization, and melting temperatures of polyethylene terephthalate (PET). A Box-Behnken statistical designed experiment was used to evaluate the effect of forming temperature, forming rate, and heat-set temperature on shrinkage, tear resistance, and thermal properties. At a forming temperature of 88/sup 0/C and heat-set temperature of 180/sup 0/C, good-quality PET parts were produced. The optimum forming time appears to be either 0.5 min or 5.0 min. In addition, inductively coupled argon plasma emission spectroscopy (ICAP) was used to determine the catalyst system for both PET sheets from two vendors.

  8. Determination of intrinsic viscosity of poly(ethylene terephthalate) using infrared spectroscopy and multivariate calibration method.

    PubMed

    Silva Spinacé, M A; Lucato, M U; Ferrão, M F; Davanzo, C U; De Paoli, M-A

    2006-05-15

    A methodology was developed to determine the intrinsic viscosity of poly(ethylene terephthalate) (PET) using diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and multivariate calibration (MVC) methods. Multivariate partial least squares calibration was applied to the spectra using mean centering and cross validation. The results were correlated to the intrinsic viscosities determined by the standard chemical method (ASTM D 4603-01) and a very good correlation for values in the range from 0.346 to 0.780dLg(-1) (relative viscosity values ca. 1.185-1.449) was observed. The spectrophotometer detector sensitivity and the humidity of the samples did not influence the results. The methodology developed is interesting because it does not produce hazardous wastes, avoids the use of time-consuming chemical methods and can rapidly predict the intrinsic viscosity of PET samples over a large range of values, which includes those of recycled materials.

  9. 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

    2011-07-08

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

  11. 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.

  12. 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

  13. Scanning-probe-microscopy of polyethylene terephthalate surface treatment by argon ion beam

    NASA Astrophysics Data System (ADS)

    Espinoza-Beltran, Francisco; Sanchez, Isaac C.; España-Sánchez, Beatriz L.; Mota-Morales, Josué D.; Carrillo, Salvador; Enríquez-Flores, C. I.; Poncin-Epaillard, Fabienne; Luna-Barcenas, Gabriel

    2015-11-01

    The effect of argon (Ar+) ion beam treatment on the surface of polyethylene terephthalate (PET) samples was studied by scanning probe microscopy (SPM) and the changes in surface topography were assessed by atomic force microscopy (AFM). Kelvin probe force microscopy (KPFM) sheds light of adhesion force between treated polymer films and a Pt/Cr probe under dry conditions, obtaining the contact potential difference of material. As a result of Ar+ ion bombardment, important surface chemical changes were detected by X-ray photoelectron spectroscopy (XPS) measurements such as chains scission and incorporation of nitrogen species. Ion beam treatment increases the surface roughness from 0.49 ± 0.1 nm to 7.2 ± 0.1 nm and modify the surface potential of PET samples, decreasing the adhesive forces from 12.041 ± 2.1 nN to 5.782 ± 0.06 nN, and producing a slight increase in the electronic work function (Φe) from 5.1 V (untreated) to 5.2 V (treated). Ar+ ion beam treatment allows to potentially changing the surface properties of PET, modifying surface adhesion, improving surface chemical changes, wetting properties and surface potential of polymers.

  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. 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.

  16. 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.

  17. 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.

  18. [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.

  19. Electroless plating of nickel phosphorous on surface-modified poly(ethylene terephthalate) films

    NASA Astrophysics Data System (ADS)

    Domenech, S. C.; Lima, E.; Drago, V.; De Lima, J. C.; Borges, N. G.; Avila, A. O. V.; Soldi, V.

    2003-12-01

    Chemical surface preparation for Ni-P electroless metallization of poly(ethylene terephthalate) (PET) films without using Chromium-based chemicals, was studied. The applicability of this method was verified by a subsequent metallization process. Thermal analysis was conducted to observe the main thermal transitions and stability of the polymer and metallized films. Contact angle analysis was performed to assess the surface hydrophilicity so as to optimize the substrate preparation process. X-ray diffraction, EDAX and SEM analysis were used to understand the composition and morphology of the polymeric substrate and Ni-P coat growing process. Adherence strength, contact sheet resistivity and optical diffuse reflection were measured on the metallized films. The time of chemical etching affects the polymer surface hydrophilicity, polymer/metal adherence strength, surface resistance and optical diffuse reflection, while Ni coating morphology is controlled by the pH of the electroless bath. High wettability of the polymer surface, adherence strength of 800 N cm -2, high optical diffuse reflection and low surface resistivity of the Ni coating, were found for films etched for 60 min. Metallizations performed at pH 7.5 produce Ni-P coatings with 12.0 wt.% phosphorous content, which were amorphous and flexible. The contact sheet resistivity of the plated films is sensitive to roughness variations of the substrate. The method proposed in this work allows the production of metallized films appropriate for the fabrication of flexible circuits.

  20. Comparison of Self-Expanding Polyethylene Terephthalate and Metallic Stents Implanted in Porcine Iliac Arteries

    SciTech Connect

    Wilczek, Krzysztof; Scheerder, Ivan de; Wang Kai; Verbeken, Eric; Piessens, Jan

    1996-05-15

    Purpose: Comparison of the biocompatibility of self-expanding polyethylene terephthalate (PET) stents with self-expanding metallic stents (Wallstents). Methods: Diameter- and length-matched PET stents and Wallstents were symmetrically implanted in the paired iliac arteries of 13 crossbred domestic swine. Stent deployment was studied angiographically and with intravascular ultrasound immediately after stent implantation. The angiographic stented lumen diameter was measured using quantitative vessel analysis before, immediately after stenting, and at 6-week follow-up. Cross-section histopathology and area morphometry were performed. Results: Immediately poststenting, intravascular ultrasound revealed proximal dislocation of 5 of the 13 PET stents, whereas all metal stents were firmly embedded at the implantation site. At 6-week follow-up, three of the remaining PET stents were totally or subtotally occluded by organized thrombus, whereas all metal stents were patent. Compared with immediately poststenting, the angiographic lumen diameter within the five remaining PET stents was reduced by 30%, and that of the metallic stents was virtually unaltered (p < 0.02). This observation was confirmed by postmortem morphometry, wherein the PET-stented vessel segments a diameter stenosis of 40% was measured vs only 9% in the metallic stents (p < 0.0001). Conclusion: PET-stent deployment is difficult to control due to the lack of radiopacity of this stent. PET stents seem to be more thrombogenic and lead to significantly more neointimal proliferation than metallic stents.

  1. The stable hydrogen and oxygen isotope variation of water stored in polyethylene terephthalate (PET) bottles.

    PubMed

    Spangenberg, Jorge E; Vennemann, Torsten W

    2008-01-01

    A set of bottled waters from a single natural spring distributed worldwide in polyethylene terephthalate (PET) bottles has been used to examine the effects of storage in plastic polymer material on the isotopic composition (delta18O and delta2H values) of the water. All samples analyzed were subjected to the same packaging procedure but experienced different conditions of temperature and humidity during storage. Water sorption and the diffusive transfer of water and water vapor through the wall of the PET bottle may cause isotopic exchange between water within the bottle and water vapor in air near the PET-water interface. Changes of about +4 per thousand for delta2H and +0.7 per thousand for delta18O have been measured for water after 253 days of storage within the PET bottle. The results of this study clearly indicate the need to use glass bottles for storing water samples for isotopic studies. It is imperative to transfer PET-bottled natural waters to glass bottles for their use as calibration material or potential international working standards.

  2. Fog Collection on Polyethylene Terephthalate (PET) Fibers: Influence of Cross Section and Surface Structure.

    PubMed

    Azad, M A K; Krause, Tobias; Danter, Leon; Baars, Albert; Koch, Kerstin; Barthlott, Wilhelm

    2017-03-22

    Fog-collecting meshes show a great potential in ensuring the availability of a supply of sustainable freshwater in certain arid regions. In most cases, the meshes are made of hydrophilic smooth fibers. Based on the study of plant surfaces, we analyzed the fog collection using various polyethylene terephthalate (PET) fibers with different cross sections and surface structures with the aim of developing optimized biomimetic fog collectors. Water droplet movement and the onset of dripping from fiber samples were compared. Fibers with round, oval, and rectangular cross sections with round edges showed higher fog-collection performance than those with other cross sections. However, other parameters, for example, width, surface structure, wettability, and so forth, also influenced the performance. The directional delivery of the collected fog droplets by wavy/v-shaped microgrooves on the surface of the fibers enhances the formation of a water film and their fog collection. A numerical simulation of the water droplet spreading behavior strongly supports these findings. Therefore, our study suggests the use of fibers with a round cross section, a microgrooved surface, and an optimized width for an efficient fog collection.

  3. 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.

  4. 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.

  5. 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.

  6. Effects of selected process parameters on the morphology of poly(ethylene terephthalate) preforms and bottles

    SciTech Connect

    Hanley, Tracey; Sutton, David; Karatchevtseva, Inna; Cookson, David; Burford, Robert; Knott, Robert

    2008-10-03

    Small-angle X-ray scattering (SAXS) studies and polarized optical microscopy were undertaken to explore possible morphological explanations for the poor mechanical strength in the petaloid bases of poly(ethylene terephthalate) bottles. With a standard commercial production line, one set of injection-molded preforms was overpacked by 1.1 wt % to investigate the effect on the molecular morphology with respect to a set of control samples. Both sets of preforms showed highly crystalline and oriented areas corresponding to the injection gate region. The main body of the control preform was amorphous, and although the overpacked preform was essentially amorphous, there was some evidence for weak crystallinity. The SAXS patterns of the bottle petaloid base blown from the corresponding preforms produced similar SAXS patterns for overpacked and control bottle bases, indicating that the commercial process is robust at least to this degree of overpacking. Optical microscopy showed detailed crystalline features around the gate region and thin crystalline layers sandwiched between a quenched skin layer in direct contact with the cold mold walls and the main flow of material into the mold.

  7. 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.

  8. 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.

  9. Improved blood compatibility of poly(ethylene terephthalate) films modified with L-arginine.

    PubMed

    Liu, Yun; Chen, Jie-Rong; Yang, Yun; Wu, Feng

    2008-01-01

    In order to improve the blood compatibility of the commonly used blood-contacting biomaterial poly(ethylene terephthalate) (PET), in this study PET films were chemically modified with L-arginine (L-Arg) by a three-step-procedure using glutaraldehyde (GA) as a cross-linker. The composition and chemical structure of PET and its change with surface modification were examined by X-ray photoelectron spectroscopy (XPS) and attenuated total reflection Fourier transform infrared (ATR-FT-IR) spectroscopy, while the change in hydrophilicity was judged by water contact angles measurement. The result of water contact measurement indicated that the modified films became more hydrophilic than PET with the contact angle decreasing from 78.5 degrees for PET to 43.7 degrees for PET-Arg. The protein adsorption on the film surface was evaluated by bicinchoninic acid assay (BCA) method, and the result showed that the L-Arg-modified films decreased the amount of protein adsorption by about 25%. The in vitro blood compatibility such as platelet adhesion (observed by scanning electron microscopy) and thrombus formation was also investigated, and the results demonstrated that the L-Arg-modified films significantly suppressed platelet adhesion and aggregation and reduced the thrombus formation by about 67% compared with PET.

  10. 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.

  11. 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.

  12. New process for preparing complex-shaped dielectric film similar to Mylar. [Polyethylene terephthalate

    SciTech Connect

    Lagasse, R.R.; Kraynik, A.M.

    1982-02-01

    A new thermoforming/heat-treatment process yields complex-shaped dielectric film having electrical and shrinkage properties similar to those of flat Mylar film. This similarity should extend to other physical properties because the new process is directly analogous to the process used to prepare Mylar. Commercially available poly(ethylene terephthalate) film is formed into a cavity at approx. 110/sup 0/C and then heat treated at approx. 180/sup 0/C. A laboratory-scale forming apparatus has produced cylindrically shaped films having depth/diameter ratio approx. 1, a tapered wall-section, and variation in wall thickness of < 3X. Evaluation of other forming methods suggests that the production rate and thickness uniformity can be improved with existing technology. Thermal shrinkage at 150/sup 0/C, 1 kHz dielectric constant from -55 to +70/sup 0/C, leakage current at 1 kV, and breakdown voltage have been measured for both the complex-shaped film and Mylar. These comparative measurements indicate that the complex-shaped film could replace the flat Mylar dielectric currently used in energy-storage capacitors. A complex-shaped energy-storage capacitor could enhance safety in certain nuclear weapon applications by allowing strong-link devices in a firing set to be enclosed by a weak link.

  13. Antimicrobial brass coatings prepared on poly(ethylene terephthalate) textile by high power impulse magnetron sputtering.

    PubMed

    Chen, Ying-Hung; Wu, Guo-Wei; He, Ju-Liang

    2015-03-01

    The goal of this work is to prepare antimicrobial, corrosion-resistant and low-cost Cu65Zn35 brass film on poly(ethylene terephthalate) (PET) fabric by high-power impulse magnetron sputtering (HIPIMS), which is known to provide high-density plasma, so as to generate a strongly adherent film at a reduced substrate temperature. The results reveal that the brass film grows in a layer-plus-island mode. Independent of their deposition time, the obtained films retain a Cu/Zn elemental composition ratio of 1.86 and exhibit primarily an α copper phase structure. Oxygen plasma pre-treatment for 1min before coating can significantly increase film adhesion such that the brass-coated fabric of Grade 5 or Grade 4-5 can ultimately be obtained under dry and wet rubbing tests, respectively. However, a deposition time of 1min suffices to provide effective antimicrobial properties for both Staphylococcus aureus and Escherichia coli. As a whole, the feasibility of using such advanced HIPIMS coating technique to develop durable antimicrobial textile was demonstrated.

  14. 78 FR 13857 - Antidumping or Countervailing Duty Order, Finding, or Suspended Investigation; Advance...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-03-01

    ... Terephthalate (Pet) Film from Dana Mermelstein, (202) 482-1391. India (A-533-824) (2nd Review). Polyethylene Terephthalate (Pet) Film from Dana Mermelstein, (202) 482-1391. Taiwan (A-583-837) (2nd Review). Countervailing Duty Proceedings Polyethylene Terephthalate (Pet) Film from Dana Mermelstein, (202) 482-1391. India...

  15. 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

  16. Materials characterization of explanted polypropylene, polyethylene terephthalate, and expanded polytetrafluoroethylene composites: spectral and thermal analysis.

    PubMed

    Cozad, Matthew J; Grant, David A; Bachman, Sharon L; Grant, Daniel N; Ramshaw, Bruce J; Grant, Sheila A

    2010-08-01

    This study utilized spectral and thermal analysis of explanted hernia mesh materials to determine material inertness and elucidate reasons for hernia mesh explantation. Composite mesh materials, comprised of polypropylene (PP) and expanded polytetrafluoroethylene (ePTFE) mesh surrounded by a polyethylene terephthalate (PET) ring, were explanted from humans. Scanning electron microscopy (SEM) was conducted to visually observe material defects while attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) was used to find chemical signs of surface degradation. Modulated differential scanning calorimetry (MDSC) and thermogravimetric analysis (TGA) gave thermal stability profiles that showed changes in heat of fusion and rate of percent weight loss, respectively. ATR-FTIR scans showed higher carbonyl peak areas as compared to pristine for 91% and 55% of ePTFE and PP explants, respectively. Ninety-one percent of ePTFE explants also exhibited higher C--H stretch peak areas. Seventy-three percent of ePTFE explants had higher heats of fusion while 64% of PP explants had lower heats of fusion with respect to their corresponding pristines. Only 9% of PET explants exhibited a lower heat of fusion than pristine. Seventy-three percent of ePTFE explants, 73% of PP explants, and only 18% of PET explants showed a decreased rate of percent weight loss as compared to pristine. The majority of the PP and ePTFE mesh explants demonstrated oxidation and crosslinking, respectively, while the PET ring exhibited breakdown at the sites of high stress. The results showed that all three materials exhibited varied degrees of chemical degradation suggesting that a lack of inertness in vivo contributes to hernia mesh failure.

  17. 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.

  18. 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.

  19. 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.

  20. Nano/micro electro-spun polyethylene terephthalate fibrous mat preparation and characterization.

    PubMed

    Hadjizadeh, Afra; Ajji, Abdellah; Bureau, Martin N

    2011-04-01

    Electro-spun polyethylene terephthalate (PET) fibrous mats are potential substrates for biotechnological and biomedical applications. In this regard, substrate characteristics including, fiber diameter, orientation and mechanical properties play an important role in controlling the interaction of substrate with biological entities. However, few studies reporting the preparation of electro-spun PET substrates with such controlled characteristics have been published. In this study, electro-spun PET fibrous mats with fiber diameters in the nanometer and micrometer range were produced by varying polymer solution concentration and flow rate. Fiber orientation within the mats was also varied by varying collector surface velocities in rotation and translation. Their morphological, mechanical, thermal and structural properties were evaluated as a function of fiber diameter and collector speed using scanning electron microscopy (SEM), a micromechanical tester, differential scanning calorimetry (DSC) and X-ray diffraction (XRD), respectively. Varying polymer solution concentration and flow rate allowed the production of matrices with fiber diameters ranging from 400 nm to 2 μm. Tensile properties increased with fiber diameter and collector surface velocity. Thermal properties of electro-spun PET fibers were different from the structure of as received raw PET in the form of pellets, revealing an amorphous structure for the entire electro-spun PET. This was also confirmed by XRD analysis. No considerable differences were observed between electro-spun PET fibers, in terms of crystalline and thermal properties, produced under various conditions. These electro-spun mats with different fiber diameters, orientation and mechanical properties can be used for various applications including tissue engineering scaffolds.

  1. 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).

  2. 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).

  3. 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.

  4. Environmentally Assisted Cracking in Silicon Nitride Barrier Films on Poly(ethylene terephthalate) Substrates.

    PubMed

    Kim, Kyungjin; Luo, Hao; Singh, Ankit K; Zhu, Ting; Graham, Samuel; Pierron, Olivier N

    2016-10-03

    A singular critical onset strain value has been used to characterize the strain limits of barrier films used in flexible electronics. However, such metrics do not account for time-dependent or environmentally assisted cracking, which can be critical in determining the overall reliability of these thin-film coatings. In this work, the time-dependent channel crack growth behavior of silicon nitride barrier films on poly(ethylene terephthalate) (PET) substrates is investigated in dry and humid environments by tensile tests with in situ optical microscopy and numerical models. The results reveal the occurrence of environmentally assisted crack growth at strains well below the critical onset crack strain and in the absence of polymer-relaxation-assisted, time-dependent crack growth. The crack growth rates in laboratory air are about 1 order of magnitude larger than those tested in dry environments (dry air or dry nitrogen). In laboratory air, crack growth rates increase from ∼200 nm/s to 60 μm/s for applied stress intensity factors, K, ranging from 1.0 to 1.4 MPa·m(1/2), below the measured fracture toughness Kc of 1.8 MPa·m(1/2). The crack growth rates in dry environments were also strongly dependent on the prior storage of the specimens, with larger rates for specimens exposed to laboratory air (and therefore moisture) prior to testing compared to specimens stored in a dry environment. This behavior is attributed to moisture-assisted cracking, with a measured power law exponent of ∼22 in laboratory air. This study also reveals that much larger densities of channel cracks develop in the humid environment, suggesting an easier initiation of channel cracks in the presence of water vapor. The results obtained in this work are critical to address the time-dependent and environmental reliability issues of thin brittle barriers on PET substrates for flexible electronics applications.

  5. 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

  6. 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.

  7. Preparation of activated carbon from waste plastics polyethylene terephthalate as adsorbent in natural gas storage

    NASA Astrophysics Data System (ADS)

    Yuliusman; Nasruddin; Sanal, A.; Bernama, A.; Haris, F.; Ramadhan, I. T.

    2017-02-01

    The main problem is the process of natural gas storage and distribution, because in normal conditions of natural gas in the gas phase causes the storage capacity be small and efficient to use. The technology is commonly used Compressed Natural Gas (CNG) and Liquefied Natural Gas (LNG). The weakness of this technology safety level is low because the requirement for high-pressure CNG (250 bar) and LNG requires a low temperature (-161°C). It takes innovation in the storage of natural gas using the technology ANG (Adsorbed Natural Gas) with activated carbon as an adsorbent, causing natural gas can be stored in a low pressure of about 34.5. In this research, preparation of activated carbon using waste plastic polyethylene terephthalate (PET). PET plastic waste is a good raw material for making activated carbon because of its availability and the price is a lot cheaper. Besides plastic PET has the appropriate characteristics as activated carbon raw material required for the storage of natural gas because the material is hard and has a high carbon content of about 62.5% wt. The process of making activated carbon done is carbonized at a temperature of 400 ° C and physical activation using CO2 gas at a temperature of 975 ° C. The parameters varied in the activation process is the flow rate of carbon dioxide and activation time. The results obtained in the carbonization process yield of 21.47%, while the yield on the activation process by 62%. At the optimum process conditions, the CO2 flow rate of 200 ml/min and the activation time of 240 minutes, the value % burn off amounted to 86.69% and a surface area of 1591.72 m2/g.

  8. 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.

  9. 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

    ... volatility for purified terephthalic acid (PTA) and mono ethylene glycol (MEG),\\37\\ the main inputs consumed... chemically different than MEG. b. Linkage Between Cost and Sales Information The Department also...

  10. 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

  11. Antimony leaching from polyethylene terephthalate (PET) plastic used for bottled drinking water.

    PubMed

    Westerhoff, Paul; Prapaipong, Panjai; Shock, Everett; Hillaireau, Alice

    2008-02-01

    Antimony is a regulated contaminant that poses both acute and chronic health effects in drinking water. Previous reports suggest that polyethylene terephthalate (PET) plastics used for water bottles in Europe and Canada leach antimony, but no studies on bottled water in the United States have previously been conducted. Nine commercially available bottled waters in the southwestern US (Arizona) were purchased and tested for antimony concentrations as well as for potential antimony release by the plastics that compose the bottles. The southwestern US was chosen for the study because of its high consumption of bottled water and elevated temperatures, which could increase antimony leaching from PET plastics. Antimony concentrations in the bottled waters ranged from 0.095 to 0.521 ppb, well below the US Environmental Protection Agency (USEPA) maximum contaminant level (MCL) of 6 ppb. The average concentration was 0.195+/-0.116 ppb at the beginning of the study and 0.226+/-0.160 ppb 3 months later, with no statistical differences; samples were stored at 22 degrees C. However, storage at higher temperatures had a significant effect on the time-dependent release of antimony. The rate of antimony (Sb) release could be fit by a power function model (Sb(t)=Sb 0 x[Time, h]k; k=8.7 x 10(-6)x[Temperature ( degrees C)](2.55); Sb 0 is the initial antimony concentration). For exposure temperatures of 60, 65, 70, 75, 80, and 85 degrees C, the exposure durations necessary to exceed the 6 ppb MCL are 176, 38, 12, 4.7, 2.3, and 1.3 days, respectively. Summertime temperatures inside of cars, garages, and enclosed storage areas can exceed 65 degrees C in Arizona, and thus could promote antimony leaching from PET bottled waters. Microwave digestion revealed that the PET plastic used by one brand contained 213+/-35 mgSb/kg plastic; leaching of all the antimony from this plastic into 0.5L of water in a bottle could result in an antimony concentration of 376 ppb. Clearly, only a small

  12. 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

  13. 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.

  14. 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.

  15. Indium tin oxide films deposited by thermionic-enhanced DC magnetron sputtering on unheated polyethylene terephthalate polymer substrate

    SciTech Connect

    Lan, Y.F.; Peng, W.C.; Lo, Y.H.; He, J.L.

    2009-08-05

    Indium tin oxide thin films were deposited onto polyethylene terephthalate substrates via thermionic enhanced DC magnetron sputtering at low substrate temperatures. The structural, optical and electrical properties of these films are methodically investigated. The results show that compared with traditional sputtering, the films deposited with thermionic emission exhibit higher crystallinity, and their optical and electrical properties are also improved. Indium tin oxide films deposited by utilizing thermionic emission exhibit an average visible transmittance of 80% and an electrical resistivity of 4.5 x 10{sup -4} {Omega} cm, while films made without thermionic emission present an average visible transmittance of 74% and an electrical resistivity of 1.7 x 10{sup -3} {Omega} cm.

  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

    2016-06-05

    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.

  17. Variable-angle ATR-FTIR studies of depth distribution of amidation in surface modified poly(ethylene terephthalate)

    NASA Astrophysics Data System (ADS)

    Avadanei, Mihaela

    2011-05-01

    Variable - angle ATR-FTIR spectroscopy was applied to the evaluation of the in-depth homogeneity of amidation within superficial layers of poly(ethylene terephthalate) (PET) surfaces. Thin films of PET were subjected to aminolysis with triethylenetetramine and tetraethylenepentamine by wet chemistry and using air plasma as precursor, respectively, in order to create surface functionalities. By varying the incidence angle of the infrared radiation, chemical changes were investigated from layers of different thicknesses. The amide II band has been selected as a marker for monitoring the aminolysis products and for depth profiling. The choice of an exponential decay of the in-depth amide distribution was justified by the quite regular decreasing of the angular absorbance with depth of penetration of the evanescent wave.

  18. Transparent ultra water-repellent poly(ethylene terephthalate) substrates fabricated by oxygen plasma treatment and subsequent hydrophobic coating

    NASA Astrophysics Data System (ADS)

    Teshima, Katsuya; Sugimura, Hiroyuki; Inoue, Yasushi; Takai, Osamu; Takano, Atsushi

    2005-05-01

    Wettability of solid surfaces with water is well-known to be governed by chemical properties and nanotextures of the surfaces. A proper nanotexture of surfaces enhances their hydrophobicity. In this study, a novel method consisting of two dry process techniques, that is, nanotexturing by an oxygen plasma treatment and subsequent hydrophobic coating by means of low temperature chemical vapor deposition or plasma-enhanced chemical vapor deposition, was employed to form ultra water-repellent polymer sheets. A nanotexture was formed on a poly(ethylene terephthalate) substrate surface via selective oxygen plasma etching. This surface nanotexture remained after the hydrophobic coatings using organosilane precursors. The surface-modified substrate was transparent and ultra water-repellent, showing a water contact angle greater than 150°.

  19. Local segmental dynamics of cis-1,4-polybutadiene, polypropylene, and polyethylene terephthalate via molecular dynamics simulations

    NASA Astrophysics Data System (ADS)

    Whitley, David; Adolf, David

    2011-03-01

    NPT molecular dynamics simulations of cis-1,4-polybutadiene, polypropylene, and polyethylene terephthalate have been performed. The simulation pressure was 1 atmosphere for all systems, with all simulation temperatures being well above each polymer's glass transition temperature. The trajectories have been analysed via autocorrelation functions (ACFs) of chord vectors spanning different numbers of chain backbone bonds. Inverse Laplace transformations of these ACFs using the CONTIN algorithm afforded the corresponding distributions of relaxation times (DRTs) for the simulated dynamics. All DRTs illustrated a peak on fast time scales corresponding to short length scale segmental motion and a peak at longer time scales corresponding to longer length scale relaxations. An intermediate peak between the fast and slow peaks appears as the relaxation dynamics of longer chord vectors are analysed. The temperature dependence of the relaxation dynamics has also been investigated.

  20. Fe-Si-Cr/PTFE magnetic composite thick films on polyethylene terephthalate sheets for near field communications by aerosol deposition.

    PubMed

    Kim, Hyung-Jun; Nam, Song-Min; Koh, Jung-Hyuk

    2014-10-01

    Thick film growth of Fe-Si-Cr/poly-tetra-fluoro-ethylene (PTFE) composite films on polyethylene terephthalate (PET) sheets was investigated by aerosol deposition (AD) as a magnetic absorber for near field communication. The Fe-Si-Cr flakes were crushed to micro flakes smaller than 1 μm after the deposition, and formed dense microstructure on the PET sheets. The Fe-Si-Cr/PTFE composite thick films using 0.2 wt.% PTFE starting powder showed dense and uniform microstructure compared to the 0.5 wt.% film. The real relative permeability /' and the imaginary permeability μ" of Fe-Si-Cr/PTFE composite thick films using the 0.2 wt.% PTFE starting powder were 13.1 and 2.9 at 13.56 MHz, respectively. In the case of 0.5 wt.%, μ' and μ" respectively decreased to 7.4 and 1.0 at 13.56 MHz caused by adding PTFE.

  1. A novel one-step synthesis for carbon-based nanomaterials from polyethylene terephthalate (PET) bottles waste.

    PubMed

    El Essawy, Noha A; Konsowa, Abdelaziz H; Elnouby, Mohamed; Farag, Hassan A

    2017-03-01

    Nowadays our planet suffers from an accumulation of plastic products that have the potential to cause great harm to the environment in the form of air, water, and land pollution. Plastic water bottles have become a great problem in the environment because of the large numbers consumed throughout the world. Certain types of plastic bottles can be recycled but most of them are not. This paper describes an economical solvent-free process that converts polyethylene terephthalate (PET) bottles waste into carbon nanostructure materials via thermal dissociation in a closed system under autogenic pressure together with additives and/or catalyst, which can act as cluster nuclei for carbon nanostructure materials such as fullerenes and carbon nanotubes. This research succeeded in producing and controlling the microstructure of various forms of carbon nanoparticles from the PET waste by optimizing the preparation parameters in terms of time, additives, and amounts of catalyst.

  2. Influence of flavour absorption by food-packaging materials (low-density polyethylene, polycarbonate and polyethylene terephthalate) on taste perception of a model solution and orange juice.

    PubMed

    Van Willige, R W G; Linssen, J P H; Legger-Huysman, A; Voragen, A G J

    2003-01-01

    The influence of flavour absorption by low-density polyethylene (LDPE), polycarbonate (PC) and polyethylene terephthalate (PET) on taste perception of a model solution containing seven flavour compounds and orange juice in glass bottles was studied with and without pieces of the respective plastic films after dark storage at 20 degrees C. Owing to absorption, the amount of flavour compounds in the model solution exposed to LDPE decreased substantially. From the model flavour solution valencene was almost completely absorbed by LDPE, followed to a lesser extent by decanal, hexyl acetate, octanal and nonanone. Less flavour compounds were absorbed from the model solution by PC and PET. In contrast to LDPE, valencene was absorbed in the lowest amounts and decanal in the highest. Limonene was readily absorbed from orange juice by LDPE, while myrcene, valencene, pinene and decanal were absorbed in smaller quantities. Only three flavour compounds were absorbed from orange juice by PC and PET in very small amounts: limonene, myrcene and decanal. Although the flavour content between controls and polymer-treated samples differed substantially, the loss of flavour compounds due to absorption by LDPE, PC and PET did not influence taste perception of a model solution and orange juice significantly up to 29 days of dark storage at 20 degrees C as determined by triangular taste panel tests.

  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. 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.

  6. 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.

  7. The effect of RGD density on osteoblast and endothelial cell behavior on RGD-grafted polyethylene terephthalate surfaces.

    PubMed

    Chollet, Celine; Chanseau, Christel; Remy, Murielle; Guignandon, Alain; Bareille, Reine; Labrugère, Christine; Bordenave, Laurence; Durrieu, Marie-C

    2009-02-01

    Hybrid materials combining polyethylene terephthalate and different types of cells (endothelial and osteoblastic cells) have been developed thanks to the covalent grafting of different densities of RGD containing peptides onto the polymer surface. Biomimetic modifications were performed by means of a three-step reaction procedure: creation of COOH functions, coupling agent grafting and the immobilization of the RGDC peptides. High resolution mu-imager was used to evaluate RGD densities (varying between 0.6 and 2.4 pmol/mm(2)) and has exhibited the stability of the surface grafted peptides when treated in harsh conditions. The efficiency of this route for biomimetic modification of a PET surface was demonstrated by measuring the adhesion of MC3T3 and HSVEC cells and by focal adhesion observation. Results obtained prove that a minimal RGDC density of 1 pmol/mm(2) is required to improve MC3T3 and HSVEC cells responses. Indeed, cells seeded onto a RGDC-modified PET with a density higher than 1 pmol/mm(2) were able to establish focal adhesion as visualized by fluorescence microscope compared to cells immobilized onto unmodified PET and RGDC-modified PET with densities lower than 1 pmol/mm(2). Moreover, the number of focal contacts was enhanced by the increase of RGDC peptide densities grafted onto the material surface. With this study we proved that the density of peptides immobilized on the surface is a very important parameter influencing osteoblast or endothelial cell adhesion and focal contact formation.

  8. Recycled poly(ethylene terephthalate) for direct food contact applications: challenge test of an inline recycling process.

    PubMed

    Franz, R; Welle, F

    2002-05-01

    Of all the plastics used for packaging, due to its low diffusivity and chemical inertness, poly(ethylene terephthalate) (PET) is one of the favoured candidate plastics for closed-loop recycling for new packaging applications. In the work reported here, a PET-recycling process was investigated with respect to its cleaning efficiency and compliance of the PET recyclate with food law. The key technology of the investigated PET-recycling process to remove contaminants consists of a predecontamination-extruder combination. At the end of the recycling process, there is either a pelletizing system or downstream equipment to produce preforms or flat sheets. Therefore, the process has two process options, an inline production of PET preforms and a batch option producing PET pellets. In the case of possible misuse of PET bottles by the consumer, the inline process produces higher concentrations in the bottle wall of the recyclate containing preforms. Owing to the dilution of the PET output material by large amounts of uncontaminated PET, the batch option is the less critical process in terms of consumer protection. Regarding an appropriate testing procedure for the evaluation of a bottle-to-bottle recycling process, both process options have their own specific requirements with respect to the design of a challenge test. A novel challenge test approach to the inline mode of a recycling process is presented here.

  9. Radiation grafting of glycidyl methacrylate and divinylbenzene onto polyethylene terephthalate fabrics for improving anti-dripping performance

    NASA Astrophysics Data System (ADS)

    Chen, Xu; Wang, Yue; Dai, Guoliang; Peng, Jing; Li, Jiuqiang; Shi, Meiwu; Zhai, Maolin

    2016-10-01

    A new kind of anti-dripping polyethylene terephthalate (PET) fabric was successfully prepared by simultaneous gamma radiation-induced grafting polymerization of glycidyl methacrylate (GMA) and divinylbenzene (DVB) onto the surface of PET fabrics. The grafting yield (GY) and anti-dripping effect were optimized by changing the total absorbed dose, dose rate, concentration and the feed ratio of GMA and DVB. The grafting yield increased with the increase of absorbed dose and GMA monomer concentration, and decreased with the dose rate. It is confirmed that PET fabrics had been modified by Fourier transform infrared spectroscopy analysis. The tensile strength and elongation at break of modified PET fabrics were improved compared with original PET fabrics. The limiting oxygen index (LOI) of modified PET fabrics with the GY of 23-25% was 21.5, which was similar to that of unmodified PET fabrics. However, the anti-dripping performance of PET fabrics was improved remarkably after radiation modification due to the crosslinking of the sidechains grafted on the PET surface. This anti-dripping fabric may be promising for fire protective clothing.

  10. 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.

  11. 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.

  12. 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

  13. Flexible IZO/Ag/IZO/Ag multilayer electrode grown on a polyethylene terephthalate substrate using roll-to-roll sputtering

    PubMed Central

    2012-01-01

    We investigated the optical, electrical, structural, and surface properties of roll-to-roll [R2R] sputter-grown flexible IZO/Ag/IZO/Ag [IAIA] multilayer films on polyethylene terephthalate substrates as a function of the top indium zinc oxide [IZO] thickness. It was found that the optical transmittance of the IAIA multilayer was significantly influenced by the top IZO layer thickness, which was grown on identical AIA multilayers. However, the sheet resistance of the IAIA multilayer was maintained between the range 5.01 to 5.1 Ω/square regardless of the top IZO thickness because the sheet resistance of the IAIA multilayer was mainly dependent on the thickness of the Ag layers. Notably, the optimized IAIA multilayer had a constant resistance change (ΔR/R0) under repeated outer bending tests with a radius of 10 mm. The mechanical integrity of the R2R-sputtered IAIA multilayer indicated that hybridization of an IZO and Ag metal layer is a promising flexible electrode scheme for the next-generation flexible optoelectronics. PMID:22222144

  14. 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.

  15. Optimization and continuous fabrication of moth-eye nanostructure array on flexible polyethylene terephthalate substrate towards broadband antireflection.

    PubMed

    Zhang, Chengpeng; Yi, Peiyun; Peng, Linfa; Ni, Jun

    2017-04-01

    Reflection loss can cause harmful effects on the performance of optoelectronic devices, such as cell phones, notebooks, displays, solar cells, and light-emitting diode (LED) devices. In order to obtain broadband antireflection (AR) properties, many researchers have utilized surface texture techniques to produce AR subwavelength structures on the interfaces. Among the AR subwavelength structures, the moth-eye nanostructure is one of the most promising structures, with the potential for commercialization in the near future. In this research, to obtain broadband AR performance, the optimization of moth-eye nanostructures was first carried out using the finite difference time domain method within the spectral ranges of 400-800 nm, including the optimization of shape, height, pitch, and residual layer thickness. In addition, the continuous production of moth-eye nanostructure array upon a flexible polyethylene terephthalate substrate was demonstrated by using the roll-to-roll ultraviolet nanoimprint lithography (R2R UV-NIL) process and anodic aluminum oxide mold, which provided a solution for the cost-effective fabrication of moth-eye nanostructure array. The AR performance of moth-eye nanostructure array obtained by the R2R UV-NIL process was also investigated experimentally, and good consistence was shown with the simulated results. This research can provide a beneficial direction for the optimization and cost-effective production of the moth-eye nanostructure array.

  16. Effects of UV Aging on the Cracking of Titanium Oxide Layer on Poly(ethylene terephthalate) Substrate: Preprint

    SciTech Connect

    Zhang, Chao; Gray, Matthew H.; Tirawat, Robert; Larsen, Ross E.; Chen, Fangliang

    2016-04-18

    Thin oxide and metal films deposited on polymer substrates is an emerging technology for advanced reflectors for concentrated solar power applications, due to their unique combination of light weight, flexibility and inexpensive manufacture. Thus far, there is little knowledge on the mechanical integrity or structural persistence of such multi-layer thin film systems under long-term environmental aging. In this paper, the cracking of a brittle titanium dioxide layer deposited onto elasto-plastic poly(ethylene terephthalate) (PET) substrate is studied through a combination of experiment and modeling. In-situ fragmentation tests have been conducted to monitor the onset and evolution of cracks both on pristine and on samples aged with ultraviolet (UV) light. An analytical model is presented to simulate the cracking behavior and to predict the effects of UV aging. Based on preliminary experimental observation, the effect of aging is divided into three aspects and analyzed independently: mechanical property degradation of the polymer substrate; degradation of the interlayer between substrate and oxide coating; and internal stress-induced cracks on the oxide coating.

  17. 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.

  18. 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.

  19. 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.

  20. Room temperature crystallization of indium tin oxide films on glass and polyethylene terephthalate substrates using rf plasma

    SciTech Connect

    Ohsaki, H.; Suzuki, M.; Shibayama, Y.; Kinbara, A.; Watanabe, T.

    2007-07-15

    The crystallization of amorphous indium tin oxide (ITO) films was achieved by rf (13.56 MHz) plasma treatment. Although the films were crystallized after 2 min, the sample temperature was lower than 90 deg. C without compulsory cooling even after 10 min of treatment and polyethylene terephthalate (PET) substrates had no damage. Plasma-crystallized sputtered ITO films have a bixbite structure and the resistivity reached to 1.6x10{sup -4} {omega}{center_dot}cm. ITO thin films have almost the same resistivity in both cases of PET and glass substrates used and plasma-treated PET ITO films have a bit higher resistivity than that of glass ITO films, while mass spectroscopy measurements indicated that ITO films deposited on PET substrates are expected to include no apparent gas species ejected from PET substrate. It was found that the plasma gas pressure is the key parameter for the effective crystallization and the appropriate gas pressure depends on the plasma gas species.

  1. Plasma treated polyethylene terephthalate/polypropylene films assembled with chitosan and various preservatives for antimicrobial food packaging.

    PubMed

    Lei, Jieqiong; Yang, Lingxiao; Zhan, Yingfei; Wang, Yuntao; Ye, Ting; Li, Yan; Deng, Hongbing; Li, Bin

    2014-02-01

    In this study, polyethylene terephthalate/polypropylene (PET/PP) films were treated via atmospheric pressure plasma, assembled with chitosan and various preservatives and applied for antimicrobial food packaging. Surface properties of these obtained films were studied by contact angle measurement, atomic force microscopy (ATM), X-ray photoelectron spectroscopy (XPS), Fourier transformed infrared spectroscopy (FT-IR) and dynamic laser scattering (DLS). The above results showed that the surface hydrophilicity and roughness of the films increased after the plasma treatment. Besides, chitosan and the preservatives were successfully assembled onto the surface of the films. In addition, the antimicrobial activities of the films against three kinds of microorganisms (Staphylococcus aureus, Bacillus subtilis and Escherichia coli) were investigated and the results indicated that the inhibition ratios against B. subtilis and E. coli reached almost 100% while the inhibition ratios against S. aureus were lower than 85%. Moreover, the accumulative release profiles of the antimicrobial substances migrating from the assembled films into the release solutions revealed that their release speed increased with the increment of temperature and acidity, but decreased with enhancing the ionic strength regulated by sodium chloride or with lowering the ionic mobility regulated by sucrose.

  2. 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.

  3. 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.

  4. The low-temperature endotherm in poly(ethylene terephthalate): partial melting and rigid amorphous fraction mobilization.

    PubMed

    Righetti, Maria Cristina; Lorenzo, Maria Laura Di; Tombari, Elpidio; Angiuli, Marco

    2008-04-10

    A detailed investigation of the low-temperature endotherm of poly(ethylene terephthalate) (PET) performed by temperature-modulated differential scanning calorimetry is presented. The origin of the small endotherm, generally observed a few degrees above the crystallization temperature in PET and in many other polymers, is a widely discussed matter. The most frequent interpretation considers it the result of partial fusion with superposition of a recrystallization process even if it has also been proposed that it can originate from enthalpic recovery connected to mobilization of the rigid amorphous fraction. In an attempt to resolve the question, a new method for the interpretation of the modulated heat-flow-rate curve resulting from a temperature modulation program is proposed. The procedure consists of the analysis of the initial points of the steady-state heat-flow-rate signals in the heating and cooling semiperiods with the temperature modulation being performed with a sawtooth profile. The study conducted in parallel on the reversing specific heat capacity and the heat-flow-rate curves, observed on heating after isothermal crystallization at various temperatures, showed that multiple processes, involving both the crystalline and the rigid amorphous fraction, overlap in the temperature range in which the low-temperature endotherm is observed. The origin of the endotherm under investigation is therefore connected with both partial fusion of the crystalline portions and enthalpy recovery subsequent to structural relaxation of the rigid amorphous fraction. An estimation of the relative percentages of the two different processes is presented and discussed.

  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. 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

    2015-05-07

    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.

  7. 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.

  8. Effects of ph ON Ni Coating on Poly(ethylene Terephthalate) Substrate by Printing Prime in Combination with Palladium Activating

    NASA Astrophysics Data System (ADS)

    Huang, Junjun; Sun, Zhiping; Huang, Hongzhi; Liu, Qi; Gao, Min; Li, Mengyu; Zhao, Feng; Chen, Zhenming

    2016-04-01

    In this work, the primer-printed and then self-assembled poly(ethylene terephthalate) (PET) sheets were plated when the bath pH increased from 7 to 11. The effects of bath pH on the structural and electrical properties of electroless nickel plating were investigated systematically using X-ray diffraction (XRD) and scanning electron microscopy (SEM). Results showed that the crystallographic structures of Ni-plated PET (NPP) sheets were face centered cubic, the preferential orientation of the coatings changes from (200) plane to (111) plane, the growth rate of plated nickel coating increased from 3.71μm/min to 8.13μm/min, the average Ni crystal size was increased from 0.23μm to 0.92μm, the average EMI-SE of NPP sheets was increased from 37.2dB to 38.6dB and the surface electrical resistivity of NPP sheets was decreased from 6235ohm ṡ cm to 0.03ohm ṡ cm with the increase of bath pH. The changes in structural and electrical properties were most possibly due to the fact that the thickness of coating increased.

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

    PubMed

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

    2015-09-04

    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.

  11. Leak detection in polyethylene terephthalate bottles filled with water and pulped and unpulped orange juice using a vacuum decay system.

    PubMed

    Sivaramakrishna, Vijaykrishna; Mehta, Anish; Schramm, Gerhard; Pascall, Melvin A

    2007-10-01

    This research evaluated an offline vacuum decay leak detection system for 1775-ml polyethylene terephthalate (PET) bottles. These bottles were filled with water and pulped and unpulped orange juice and induction sealed with an aluminum liner and an outer 38-mm continuous thread polypropylene cap. The objectives of this study were to evaluate (i) minimum leak size sensitivity of the instrument; (ii) ability to identify weak but nonleaking seals; (iii) effect of varying fill heights on the equipment's sensitivity; and (iv) percentage of false-positive and negative results likely to be obtained during a normal test run. To meet these objectives, leaks 5, 10, 15, 20, 30, 40, and 50 microm were created in the PET bottles. A second set of bottles was induction sealed at high voltage and 1, 1.5, 2, 2.5, 3, 3.5, and 4 s of dwell time. A third set of bottles with good seals was filled with differing headspace measurements of brimful, 1, 2, 3, 4, and 5 cm. After optimizing the equipment, leak tests on random sets of leaking and nonleaking bottles showed 0.0% false-positive and 0.0% negative identifications. Results showed 5-microm minimum leak size detection for bottles filled with all products. Optimum seal conditions were >2 but <3 s at high voltage. Product fill heights >2 to < or =3 cm did not affect the efficiency of the equipment. These results show that this vacuum decay system has potential for use in identifying leaks in PET bottles used for food packaging.

  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.

  13. Characteristics and anticoagulation behavior of polyethylene terephthalate modified by C2H2 plasma immersion ion implantation-deposition

    NASA Astrophysics Data System (ADS)

    Wang, J.; Pan, C. J.; Kwok, S. C. H.; Yang, P.; Chen, J. Y.; Wan, G. J.; Huang, N.; Chu, P. K.

    2004-01-01

    Acetylene (C2H2) plasma immersion ion implantation-deposition (PIII-D) is conducted on polyethylene terephthalate (PET) to improve its blood compatibility. The structural and physicochemical properties of the modified surface are characterized by, Raman spectroscopy, x-ray photoelectron spectroscopy (XPS), and static contact angle measurement. Atomic force microscopy discloses that the average roughness (Ra) of film surface decreases from 58.9 nm to 11.4 nm after C2H2 PIII-D treats PET. Attenuated total reflection Fourier transform infrared spectroscopy shows that the specfic adsorption peaks for PET decrease after ion implantation and deposition. Raman spectroscopy indicates that a thin amorphous polymerlike carbon (PLC) film is formed in the PET. The effects of the surface modification on the chemical bonding of C, H, and O are examined by XPS and the results show that the ratio of sp3 C-C to sp2 C=C is 0.25. After C2H2 PIII-D, the polar component γp of surface energy increases from 2.4 mN/m to 12.3 mN/m and γp/γd increases from 0.06 to 0.35. The wettability of the modified surfaces is improved. Scanning electron microscopy and optical microscopy reveal that the amounts of adhered, aggregated and morphologically changed platelets are reduced by the deposition of an amorphous polymer-like carbon film. The thrombin time, prothrombin time, and activated partial thromboplastin time of the modified PET are longer than those of the untreated PET. Our result thus shows that the amorphous PLC film deposited on the PET surface by C2H2 PIII-D improves platelet adhesion and activation. .

  14. 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.

  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. Efficient immobilization and patterning of biomolecules on poly(ethylene terephthalate) films functionalized by ion irradiation for biosensor applications.

    PubMed

    Hwang, In-Tae; Kuk, In-Seol; Jung, Chan-Hee; Choi, Jae-Hak; Nho, Young-Chang; Lee, Young-Moo

    2011-07-01

    The surface of a poly(ethylene terephthalate) (PET) film was selectively irradiated with proton beams at various fluences to generate carboxylic acid groups on the surface; the resulting functionalized PET surface was then characterized in terms of its wettability, chemical structure, and chemical composition. The results revealed that (i) carboxylic acid groups were successfully generated in the irradiated regions of the PET surface, and (ii) their relative amounts were dependent on the fluence. A capture biomolecule, anthrax toxin probe DNA, was selectively immobilized on the irradiated regions on the PET surface. Cy3-labeled DNA as a target biomolecule was then hybridized with the probe DNA immobilized on the PET surface. Liver-cancer-specific α-fetoprotein (AFP) antigen, as a target biomolecule, was also selectively immobilized on the irradiated regions on the PET surface. Texas Red-labeled secondary antibody was then reacted with an AFP-specific primary antibody prebound to the AFP antigen on the PET surface for the detection of the target antigen, using an indirect immunoassay method. The results revealed that (i) well-defined micropatterns of biomolecules were successfully formed on the functionalized PET surfaces and (ii) the fluorescence intensity of the micropatterns was dependent mainly on the concentrations of the target DNA hybridized to the probe DNA and the target AFP antigen immobilized on the PET films. The lowest detectable concentrations of the target DNA and target AFP antigen in this study were determined to be 4 and 16 ng/mL, respectively, with the PET film prepared at a fluence of 5 × 10(14) ions/cm(2).

  17. Effect of Tris, MOPS, and phosphate buffers on the hydrolysis of polyethylene terephthalate films by polyester hydrolases.

    PubMed

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

    2016-09-01

    The enzymatic degradation of polyethylene terephthalate (PET) occurs at mild reaction conditions and may find applications in environmentally friendly plastic waste recycling processes. The hydrolytic activity of the homologous polyester hydrolases LC cutinase (LCC) from a compost metagenome and TfCut2 from Thermobifida fusca KW3 against PET films was strongly influenced by the reaction medium buffers tris(hydroxymethyl)aminomethane (Tris), 3-(N-morpholino)propanesulfonic acid (MOPS), and sodium phosphate. LCC showed the highest initial hydrolysis rate of PET films in 0.2 m Tris, while the rate of TfCut2 was 2.1-fold lower at this buffer concentration. At a Tris concentration of 1 m, the hydrolysis rate of LCC decreased by more than 90% and of TfCut2 by about 80%. In 0.2 m MOPS or sodium phosphate buffer, no significant differences in the maximum initial hydrolysis rates of PET films by both enzymes were detected. When the concentration of MOPS was increased to 1 m, the hydrolysis rate of LCC decreased by about 90%. The activity of TfCut2 remained low compared to the increasing hydrolysis rates observed at higher concentrations of sodium phosphate buffer. In contrast, the activity of LCC did not change at different concentrations of this buffer. An inhibition study suggested a competitive inhibition of TfCut2 and LCC by Tris and MOPS. Molecular docking showed that Tris and MOPS interfered with the binding of the polymeric substrate in a groove located at the protein surface. A comparison of the K i values and the average binding energies indicated MOPS as the stronger inhibitor of the both enzymes.

  18. Evaluation of removal of model particulate and oily soils from poly(ethylene terephthalate) films by microscopic image analysis.

    PubMed

    Gotoh, Keiko; Yu, Nagai; Tagawa, Yumiko

    2013-01-01

    The soil removal behavior from poly(ethylene terephthalate) (PET) films was investigated using a microscopic image analysis system. Carbon black or stearic acid as a model soil was deposited onto a PET film. The PET film was cleaned in various aqueous and non-aqueous solutions by applying stirring or frequency-modulated ultrasound as a mechanical action of soil removal. The amounts of soil deposited on the PET film before and after cleaning were obtained via binary processing of microscopic images, from which the removal efficiency was calculated. Most of the carbon black was deposited on the PET film as submicron aggregates and ultrasound removed them efficiently in a short time, even for relatively smaller aggregates. The removal efficiencies with stirring were less than ca. 10% in all solutions, whereas the removal using ultrasound had high efficiencies that exceeded 80% in the surfactant-free systems. In the case of stearic acid, the removal efficiency with stirring was below 30% in the aqueous solutions, although stearic acid was removed completely in ethanol and n-decane. For ultrasonic cleaning, the removal efficiencies of stearic acid in aqueous solutions became 2-3 times as large as those with the stirring action. To improve soil release in aqueous solutions, the PET film was treated by the dry processing using an atmospheric pressure plasma jet (APPJ) equipment. The wettability and the surface free energy of the PET film were found to increase due to surface oxidation via the APPJ treatment, which resulted in enhanced removal of carbon black and stearic acid in any aqueous solutions.

  19. Quantitative evaluation of radiation damage to polyethylene terephthalate by soft X-rays and high-energy electrons.

    PubMed

    Wang, Jian; Botton, Gianluigi A; West, Marcia M; Hitchcock, Adam P

    2009-02-19

    The chemical changes and absolute rates in radiation damage to polyethylene terephthalate (PET) caused by soft X-rays and energetic electrons have been measured using a scanning transmission X-ray microscope (STXM). Electron beam damage at two different dose rates and a range of doses was performed in an 80 keV transmission electron microscope (TEM). The STXM beam was used to create damage patterns with systematically varied doses of monochromatic soft X-rays on an adjacent piece of the same PET sample. NEXAFS spectroscopy at the C 1s and O 1s edges was used to study the chemistry of the radiation damage and to determine quantitative critical doses for PET damage by both types of radiation. The spectral changes were similar for damage by electrons and X-rays, indicating the radiation chemistry is dominated by secondary processes, not the primary event. The critical dose for chemical changes determined from C 1s spectral features is 4.2(6) x 10(8) Gy and was the same for soft X-rays and electrons within measurement uncertainties. The critical dose for specific damage processes (as defined by changes in several different, bond-specific spectral features) was found to be similar in the C 1s region and was comparable between C 1s and O 1s edges for electron beam damage. There were statistically different critical doses for soft X-ray damage as probed by changes in O 1s spectral features related to carbonyl and ester bonds.

  20. 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

  1. Characteristics of radio frequency-sputtered ZnS on the flexible polyethylene terephthalate (PET) substrate.

    PubMed

    Yoo, Dongjun; Choi, Moon-Suk; Chung, Chulwon; Heo, Seung Chan; Kim, Dohyung; Choi, Changhwan

    2013-12-01

    Zinc sulfide (ZnS) thin film was deposited on the flexible polyethylene-terephtalate (PET) polymer substrate by radio frequency (RF) magnetron sputtering system. ZnS film has a critical thickness range affecting crystal structure where it shows preferred orientation with intensity peak of X-ray diffractometer at 28.4 degrees for ZnS thinner than 200 nm while hexagonal wurtzite and cubic zinc-blend (101) are co-existed for film thicker than 200 nm. Optical band gap energy (Eg) decreases with increasing RF-powers, resulting from increase in film thickness. Eg of ZnS films on PET is 3.68-3.86 eV, which is lower than that of ZnS on the rigid substrate by 0.27-0.28 eV. This is attributed to amount of incorporated oxygen to ZnS material as well as residual strain and disorder of grain boundary. Transmittance of ZnS on PET degrades due to surface defects and complex internal structure. Energy dispersive spectroscopy reveals out that ZnS film does not have a unity of Zn to S ratio, but it is close to stoichiometric composition with increasing thickness.

  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. 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.

  4. 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.

  5. Toxic effects of polyethylene terephthalate microparticles and Di(2-ethylhexyl)phthalate on the calanoid copepod, Parvocalanus crassirostris.

    PubMed

    Heindler, Franz M; Alajmi, Fahad; Huerlimann, Roger; Zeng, Chaoshu; Newman, Stephen J; Vamvounis, George; van Herwerden, Lynne

    2017-03-30

    Large amounts of plastic end up in the oceans every year where they fragment into microplastics over time. During this process, microplastics and their associated plasticizers become available for ingestion by different organisms. This study assessed the effects of microplastics (Polyethylene terephthalate; PET) and one plasticizer (Di(2-ethylhexyl)phthalate; DEHP) on mortality, productivity, population sizes and gene expression of the calanoid copepod Parvocalanus crassirostris. Copepods were exposed to DEHP for 48h to assess toxicity. Adults were very healthy following chemical exposure (up to 5120µg L(-1)), whereas nauplii were severely affected at very low concentrations (48h LC50value of 1.04 ng L(-1)). Adults exposed to sub-lethal concentrations of DEHP (0.1-0.3µg L(-1)) or microplastics (10,000-80,000 particles mL(-1)) exhibited substantial reductions in egg production. Populations were exposed to either microplastics or DEHP for 6 days with 18 days of recovery or for 24 days. Populations exposed to microplastics for 24 days significantly depleted in population size (60±4.1%, p<0.001) relative to controls, whilst populations exposed for only 6 days (with 18 days of recovery) experienced less severe depletions (75±6.0% of control, p<0.05). Populations exposed to DEHP, however, exhibited no recovery and both treatments (6 and 24 days) yielded the same average population size at the termination of the experiment (59±4.9% and 59±3.4% compared to control; p<0.001). These results suggest that DEHP may induce reproductive disorders that can be inherited by subsequent generations. Histone 3 (H3) was significantly (p<0.05) upregulated in both plastic and DEHP treatments after 6 days of exposure, but not after 18 days of recovery. Hsp70-like expression showed to be unresponsive to either DEHP or microplastic exposure. Clearly, microplastics and plasticizers pose a serious threat to zooplankton and potentially to higher trophic levels.

  6. The Effect of Sodium Hyaluronate on Ligamentation and Biomechanical Property of Tendon in Repair of Achilles Tendon Defect with Polyethylene Terephthalate Artificial Ligament: A Rabbit Tendon Repair Model

    PubMed Central

    Li, Shengkun; Jiang, Jia; Chen, Shiyi

    2016-01-01

    The Achilles tendon is the most common ruptured tendon of human body. Reconstruction with polyethylene terephthalate (PET) artificial ligament is recommended in some serious cases. Sodium hyaluronate (HA) is beneficial for the healing of tendon injuries. We aimed to determine the effect of sodium hyaluronate in repair of Achilles tendon defect with PET artificial ligament in an animal tendon repair model. Sixteen New Zealand White rabbits were divided into two groups. Eight rabbits repaired with PET were assigned to PET group; the other eight rabbits repaired with PET along with injection of HE were assigned to HA-PET group. All rabbits were sacrificed at 4 and 8 weeks postoperatively for biomechanical and histological examination. The HA-PET group revealed higher biomechanical property compared with the PET group. Histologically, more collagen tissues grew into the HA-PET group compared with PET group. In conclusion, application of sodium hyaluronate can improve the healing of Achilles tendon reconstruction with polyethylene terephthalate artificial ligament. PMID:28105436

  7. Low-cost, acid/alkaline-resistant, and fluorine-free superhydrophobic fabric coating from onionlike carbon microspheres converted from waste polyethylene terephthalate.

    PubMed

    Hu, Haibo; Gao, Lei; Chen, Changle; Chen, Qianwang

    2014-01-01

    Onionlike carbon microspheres composed of many nanoflakes have been prepared by pyrolyzing waste polyethylene terephthalate in supercritical carbon dioxide at 650 °C for 3 h followed by subsequent vacuum annealing at 1500 °C for 0.5 h. The obtained onionlike carbon microspheres have very high surface roughness and exhibit unique hydrophobic properties. Considering their structural similarities with a lotus leaf, we further developed a low-cost, acid/alkaline-resistant, and fluorine-free superhydrophobic coating strategy on fabrics by employing the onionlike carbon microspheres and polydimethylsiloxane as raw materials. This provides a novel technique to convert waste polyethylene terephthalate to valuable carbon materials. At the same time, we demonstrate a novel application direction of carbon materials by taking advantage of their unique structural properties. The combination of recycling waste solid materials as carbon feedstock for valuable carbon material production, with the generation of highly value-added products such as superhydrophobic fabrics, may provide a feasible solution for sustainable solid waste treatment.

  8. 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

  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. Hybrid radio-frequency/direct-current plasma-enhanced chemical vapor deposition system for deposition on inner surfaces of polyethylene terephthalate bottles

    SciTech Connect

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

    2009-12-15

    A hybrid radio-frequency (rf)/direct-current (dc) system has been developed to control the biasing effects during deposition of diamondlike carbon (DLC) films onto the inner wall of polyethylene terephthalate (PET) bottles. An additional dc bias is coupled to the rf electrode to produce the effect of equivalent rf self-biasing. This allows more flexible control of the deposition of the DLC films which are intended to improve the gas barrier characteristics. The experimental results demonstrate that the additional dc bias improves the adhesion strength between the DLC film and PET, although the enhancement in the gas barrier properties is not significantly larger compared to the one without dc bias. The apparatus and methodology have practical importance in the food and beverage industry.

  11. Possibility of Solid-State Graft Copolymerization on Poly(ethylene terephthalate) Films by Plasma Irradiation and Effects of Surface Modification

    NASA Astrophysics Data System (ADS)

    Narushima, Kazuo; Matsuda, Noriko; Mizutani, Chie; Yamashita, Nanami; Inagaki, Norihiro; Iio, Kokoro; Isono, Yoshihiro; Islam, Mohammed Rafiqul

    2007-07-01

    A solid-state graft copolymerization for poly(ethylene terephthalate) (PET) films was proposed for a new surface modification technique. The functional groups included in graft monomers can be introduced on a PET surface. Allylbiguanide hydrochloric acid salt (ABG), N-methylol acrylamide (NM-AAm), and N-isopropyl acrylamide (NIP-AAm) were used as graft monomers. This technique led to a large change in the N/C atomic ratio on the PET film surfaces, which shows that nitrogen functional groups were introduced on PET surfaces. On the grafted PET films, a new N 1s spectrum appeared. This N 1s spectrum contained two components, namely, amino and amido groups, which suggests that the two groups were introduced onto the PET surfaces. In particular, isopropyl groups were introduced on the PET surface in the case of NIP-AAm. The formation of these functional groups demonstrated changes in the surface properties of PET, such as improved wettability.

  12. Characterization of polyester films used in capacitors. 2: Effects of heat treatments on transient and steady-state charging currents in polyethylene terephthalate thin films

    NASA Astrophysics Data System (ADS)

    Thielen, A.; Cerfontaine, J.; Niezette, J.; Feyder, G.; Vanderschueren, J.

    1994-10-01

    The effects of various heat treatments performed before or after the vacuum deposition of aluminum electrodes on the charging currents flowing through polyethylene terephthalate (PET) thin films (6 and 12 micrometers) were studied. The amorphous phase of the PET films was characterized by the use of thermally stimulated current/relaxation map analysis spectrometry, allowing precise determination of thermodynamic and thermokinetic parameters. Density measurements were used to calculate the rate of crystallinity achieved after annealing. A correlation was found between the relaxation parameters of the alpha dipolar relaxation of PET, the rate of crystallinity, and the properties of the charging currents observed from room temperature to 200 C. Strain-induced crystallization has been put forward to account for the experimental evidences.

  13. Low-temperature layer transfer of midair cavity silicon films to a poly(ethylene terephthalate) substrate by meniscus force

    NASA Astrophysics Data System (ADS)

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

    2014-01-01

    A single-crystalline-silicon (c-Si) layer (supported by columns on a starting Si-on-insulator wafer) and a counter-poly(ethylene terephthalate) (PET) substrate were placed in close face-to-face contact, and pure water was sandwiched in between the c-Si layer and the PET substrate. The samples formed in this manner were heated on a hot plate at 80 °C. By the meniscus force generated during the evaporation of the sandwiched water from the samples, the c-Si films were completely transferred to the PET substrate. A (100)-oriented c-Si thin film that shows good adhesion was successfully formed on PET substrates at low process temperatures.

  14. 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.

  15. 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.

  16. 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

  17. 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.

  18. A novel easy-driving and easy-signal-processing electrostatic field sensor based on a piezoresistance and polyethylene terephthalate lever

    NASA Astrophysics Data System (ADS)

    Bai, Minyu; Zhao, Yulong; Jiao, Binbin; Zhai, Xiaoshe; Geng, Yingsan

    2017-03-01

    A novel electrostatic field sensor with compact structure and a simple signal processing circuit is proposed in this paper. The sensor is based on a piezoresistive force meter and a lathy polyethylene terephthalate (PET) lever for electrostatic force generation and transformation. The force meter with a rectangular membrane supported by four beams was fabricated and one end of the PET lever was attached to the center of the membrane surface. The other end of the lever was free for electrostatic force generation. Only a low voltage DC source was required for the whole sensor, rather than sophisticated driving circuits. The lever magnified the electrostatic force effecting upon the force meter, and thus the output of the sensor was large enough for a simple processing circuit to be sufficient, rather than requiring complicated instruments. Characteristics of the sensor formation make it appropriate to adopt this sensor in various applications, in particular in high voltage power systems monitoring and meteorology measurements. The experiment results showed agreement with simulation results of the sensor. Sensitivity of the prototype of this sensor was 0.06  √mV (kV · m-1)-1 which can be greatly promoted by design optimization and fabrication improvement.

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

    PubMed Central

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

    2013-01-01

    This study investigates the impact of polystyrene sodium sulfonate (PolyNaSS) grafting onto the osseointegration 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 testing 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 nongrafted 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

  20. Programme on the recyclability of food-packaging materials with respect to food safety considerations: polyethylene terephthalate (PET), paper and board, and plastics covered by functional barriers.

    PubMed

    Franz, R

    2002-01-01

    Stimulated by new ecology-driven European and national regulations, news routes of recycling waste appear on the market. Since food packages represent a large percentage of the plastics consumption and since they have a short lifetime, an important approach consists in making new packages from post-consumer used packages. On the other hand, food-packaging regulations in Europe require that packaging materials must be safe. Therefore, potential mass transfer (migration) of harmful recycling-related substances to the food must be excluded and test methods to ensure the safety-in-use of recycled materials for food packaging are needled. As a consequence of this situation, a European research project FAIR-CT98-4318, with the acronym 'Recyclability', was initiated. The project consists of three sections each focusing on a different class of recycled materials: polyethylene terephthalate (PET), paper and board, and plastics covered by functional barriers. The project consortium consists of 28 project members from 11 EU countries. In addition, the project is during its lifetime in discussion with the US Food and Drug Administrations (FDA) to consider also US FDA regulatory viewpoints and to aim, as a consequence, to harmonizable conclusions and recommendations. The paper introduces the project and presents an overview of the project work progress.

  1. 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.

  2. High-resolution poly(ethylene terephthalate) (PET) hot embossing at low temperature: thermal, mechanical, and optical analysis of nanopatterned films.

    PubMed

    Cecchini, Marco; Signori, Francesca; Pingue, Pasqualantonio; Bronco, Simona; Ciardelli, Francesco; Beltram, Fabio

    2008-11-04

    In this work we present controlled, low-damage nanotopographic surface modification of poly(ethylene terephthalate) (PET). High-resolution nanopatterning over macroscopic areas was performed by " low-temperature" hot embossing lithography (HEL). While for standard HEL the temperature is typically raised up to many tens of Celsius degrees above the polymer glass transition temperature (Tg), we demonstrate optimal results at a temperature very close to the bulk Tg of PET (72 degrees C). Nanopits and nanobarcodes were transferred onto the surface of PET commercial sheets, demonstrating reliable sub-100 nm resolution over macroscopic areas. Sample optical, mechanical, and thermal characteristics were systematically analyzed before and after embossing at low (75 degrees C) and high (150 degrees C) temperature by attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, tensile tests, and differential scanning calorimetry (DSC). We show that, while conventional high-temperature HEL can lead to dramatic degradation of the polymer in terms of transparency, flexibility, and crystallinity content, our low-temperature process fully maintains original surface and bulk substrate properties.

  3. 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.

  4. Ca2+ and Mg2+ binding site engineering increases the degradation of polyethylene terephthalate films by polyester hydrolases from Thermobifida fusca.

    PubMed

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

    2015-04-01

    Several bacterial polyester hydrolases are able to hydrolyze the synthetic polyester polyethylene terephthalate (PET). For an efficient enzymatic degradation of PET, reaction temperatures close to the glass transition temperature of the polymer need to be applied. The esterases TfH, BTA2, Tfu_0882, TfCut1, and TfCut2 produced by the thermophilic actinomycete Thermobifida fusca exhibit PET-hydrolyzing activity. However, these enzymes are not sufficiently stable in this temperature range for an efficient degradation of post-consumer PET materials. The addition of Ca2+ or Mg2+ cations to the enzymes resulted in an increase of their melting points between 10.8 and 14.1°C determined by circular dichroism spectroscopy. The thermostability of the polyester hydrolases was sufficient to degrade semi-crystalline PET films at 65°C in the presence of 10 mM Ca2+ and 10 mM Mg2+ resulting in weight losses of up to 12.9% after a reaction time of 48 h. The residues Asp174, Asp204, and Glu253 were identified by molecular dynamics simulations as potential binding residues for the two cations in TfCut2. This was confirmed by their substitution with arginine, resulting in a higher thermal stability of the corresponding enzyme variants. The generated variants of TfCut2 represent stabilized catalysts suitable for PET hydrolysis reactions performed in the absence of Ca2+ or Mg2+.

  5. Application of sample-sample two-dimensional correlation spectroscopy to determine the glass transition temperature of poly(ethylene terephthalate) thin films.

    PubMed

    Hu, Yun; Zhang, Ying; Li, Boyan; Ozaki, Yukihiro

    2007-01-01

    The glass transition temperatures (Tg) of poly(ethylene terephthalate) (PET) thin films with different thicknesses are determined by analyzing their in situ reflection-absorption infrared (RAIR) spectra measured over a temperature range of 28 to 84 degrees C. The criterion of standard deviation of the covariance matrices is used as a graphical indicator for the determination of the Tg present in the sample-sample two-dimensional (2D) correlation spectra calculated from the temperature-dependent RAIR spectra. After two data pretreatments of the first derivative of the spectral absorbance versus temperature and the mean normalization over the wavenumbers are sequentially carried out on the RAIR spectra, an abrupt change of the first-derivative correlation spectra with respect to temperature is quickly obtained. It reflects the temperature at which the apparent intensity changes in pertinent absorption bands of PET thin films take place due to the dramatic segmental motion of PET chain conformation. The Tg of the thin PET films is accordingly determined. The results reveal that it decreases with a great dependence on the film thickness and that sample-sample 2D correlation spectroscopy enables one to determine the transition temperature of polymer thin films in an easy and valid way.

  6. Silk fibroin immobilization on poly(ethylene terephthalate) films: comparison of two surface modification methods and their effect on mesenchymal stem cells culture.

    PubMed

    Liang, Meini; Yao, Jinrong; Chen, Xin; Huang, Lei; Shao, Zhengzhong

    2013-04-01

    Silk fibroin (SF) has played a curial role for the surface modification of conventional materials to improve the biocompatibility, and SF modified poly(ethylene terephthalate) (PET) materials have potential applications on tissue engineering such as artificial ligament, artificial vessel, artificial heart valve sewing cuffs dacron and surgical mesh engineering. In this work, SF was immobilized onto PET film via two different methods: 1) plasma pretreatment followed by SF dip coating (PET-SF) and 2) plasma-induce acrylic acid graft polymerization and subsequent covalent immobilization of SF on PET film (PET-PAA-SF). It could be found that plasma treatment provided higher surface roughness which was suitable for further SF dip coating, while grafted poly(acrylic acid) (PAA) promised the covalent bonding between SF and PAA. ATR-FTIR adsorption band at 3284 cm(-1), 1623 cm(-1) and 1520 cm(-1) suggested the successful introduction of SF onto PET surface, while the amount of immobilized SF of PET-SF was higher than PET-PAA-SF according to XPS investigation (0.29 vs 0.23 for N/C ratio). Surface modified PET film was used as substrate for mesenchymal stem cells (MSCs) culture, the cells on PET-SF surface exhibited optimum density compared to PET-PAA-SF according to CCK-8 assays, which indicated that plasma pretreatment followed by SF dip coating was a simple and effective way to prepare biocompatible PET surface.

  7. Broad-band conductivity and dielectric spectroscopy of composites of multiwalled carbon nanotubes and poly(ethylene terephthalate) around their low percolation threshold.

    PubMed

    Nuzhnyy, D; Savinov, M; Bovtun, V; Kempa, M; Petzelt, J; Mayoral, B; McNally, T

    2013-02-08

    Composites of multiwalled carbon nanotubes with poly(ethylene terephthalate) (PET-MWCNT) with up to 3 vol% MWCNTs were prepared and characterized by broad-band AC conductivity and dielectric spectroscopy up to the infrared range using several techniques. A very low electrical percolation threshold of 0.07 vol% MWCNTs was revealed from the low-frequency conductivity plateau as well as from DC conductivity, whose values show the same critical power dependence on MWCNT concentration with the exponent t = 4.3. Above the plateau, the AC conductivity increases with frequency up to the THz range, where it becomes overlapped with the absorption of vibrational modes. The temperature dependence down to ~5 K has shown semiconductor behaviour with a concentration-independent but weakly temperature-dependent small activation energy of ~3 meV. The behaviour is compatible with the previously suggested fluctuation-induced tunnelling conductivity model through a thin (~1 nm) polymer contact layer among the adjacent MWCNTs within percolated clusters. At higher frequencies, deviations from the simple universal conductivity behaviour are observed, indicating some distribution of energy barriers for an electron hopping mechanism.

  8. 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.

  9. 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.

  10. Radiation induced deposition of copper nanoparticles inside the nanochannels of poly(acrylic acid)-grafted poly(ethylene terephthalate) track-etched membranes

    NASA Astrophysics Data System (ADS)

    Korolkov, Ilya V.; Güven, Olgun; Mashentseva, Anastassiya A.; Atıcı, Ayse Bakar; Gorin, Yevgeniy G.; Zdorovets, Maxim V.; Taltenov, Abzal A.

    2017-01-01

    Poly(ethylene terephthalate) PET, track-etched membranes (TeMs) with 400 nm average pore size were UV-grafted with poly(acrylic acid) (PAA) after oxidation of inner surfaces by H2O2/UV system. Carboxylate groups of grafted PAA chains were easily complexed with Cu2+ ions in aqueous solutions. These ions were converted into metallic copper nanoparticles (NPs) by radiation-induced reduction of copper ions in aqueous-alcohol solution by gamma rays in the dose range of 46-250 kGy. Copper ions chelating with -COOH groups of PAA chains grafted on PET TeMs form polymer-metal ion complex that prevent the formation of agglomerates during reduction of copper ions to metallic nanoparticles. The detailed analysis by X-Ray diffraction technique (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX) confirmed the deposition of copper nanoparticles with the average size of 70 nm on the inner surface of nanochannels of PET TeMs. Samples were also investigated by FTIR, ESR spectroscopies to follow copper ion reduction.

  11. Manipulation of chemical composition and architecture of non-biodegradable poly(ethylene terephthalate)/chitosan fibrous scaffolds and their effects on L929 cell behavior.

    PubMed

    Veleirinho, Beatriz; Berti, Fernanda V; Dias, Paulo F; Maraschin, Marcelo; Ribeiro-do-Valle, Rosa M; Lopes-da-Silva, José A

    2013-01-01

    Microporous, non-woven fibrous scaffolds made of poly(ethylene terephthalate) and chitosan were produced by electrospinning. Fiber morphology, diameter, pore size, and wettability were manipulated by varying the chemical composition of the electrospinning solution, i.e. chitosan concentration and molecular weight, and by post-electrospinning treatment with glutaraldehyde. In vitro studies were conducted using a fibroblast cell line toward a comprehensive understanding of how scaffolds characteristics can modulate the cell behavior, i.e. viability, adhesion, proliferation, extracellular matrix secretion, and three-dimensional colonization. Substantial differences were found as a result of scaffold morphological changes. Higher levels of adhesion, spreading, and superficial proliferation were achieved for scaffolds with smaller fiber and pore diameters while cell penetration and internal colonization were enhanced for scaffolds with larger pores. Additionally, the available area for cell adhesion, which is related to fiber and pore size, was a crucial factor for the viability of L929 cells. This paper provides significant insights for the development and optimization of electrospun scaffolds toward an improved biological performance.

  12. Quantitative investigation of the photodegradation of polyethylene terephthalate film by friction force microscopy, contact-angle goniometry, and X-ray photoelectron spectroscopy.

    PubMed

    Hurley, Claire R; Leggett, Graham J

    2009-08-01

    Studies of the UV-induced photodegradation of poly(ethylene terephthalate) (PET) have been carried out using contact-angle goniometry, X-ray photoelectron spectroscopy (XPS), and friction force microscopy (FFM). The advancing contact angle of water, theta, decreased following exposure of free-standing PET films to UV light. Measurements of surface friction by FFM showed that the coefficient of friction mu increased as the degradation proceeded, reaching a limiting value after ca 200 min, in agreement with the contact angle data. Using a modified form of the Cassie equation, a quantitative analysis of the extent of modification could be carried out. There was a very close correlation between the coefficient of friction determined by FFM and the value of cos theta. XPS provided more detailed information on surface bonding that also correlated closely with the FFM data. Although FFM provides quantitative data on surface modification with nanometer-scale spatial resolution, it does not provide detailed structural information such as is provided by XPS. The oxygen content at the surface was found to increase as photo-generated radicals within the PET reacted with atmospheric oxygen. Increases in both ester and carbonyl contributions within XPS data accompanied this increase. It was concluded that the photodegradation process follows mainly Norrish type I reaction pathways, following previous work by Fechine et al and Grosstete et al.

  13. 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.

  14. Comparison of bacterial adhesion to dental materials of polyethylene terephthalate (PET) and polymethyl methacrylate (PMMA) using atomic force microscopy and scanning electron microscopy.

    PubMed

    Fang, Jie; Wang, Chuanyong; Li, Yifei; Zhao, Zhihe; Mei, Li

    2016-11-01

    The aim of this study was to compare the bacterial adhesion to denture materials of polyethylene terephthalate (PET) and polymethyl methacrylate (PMMA) using atomic force microscopy and scanning electron microscopy. The adhesion forces of living Streptococcus sanguinis and Streptococcus mutans to PET and PMMA were directly measured using atomic force microscopy (AFM) in liquid. Streptococcal biofilms formed on the two material surfaces were investigated and compared using scanning electron microscopy (SEM) and colony-forming units (CFU) counting. Surface roughness and hydrophobicity of PET and PMMA were also measured. The results showed that PET surfaces were significantly smoother and more hydrophilic than PMMA surfaces both with and without a salivary film (p < 0.01). The adhesion forces of S. sanguinis and S. mutans to PET surfaces were significantly stronger than to PMMA surfaces in the absence of a salivary film (p < 0.01). In the presence of a salivary film, the adhesion forces of both bacterial strains to PET and PMMA were significantly decreased (p < 0.01). The adhesion forces of S. mutans to PET surfaces (0.14 nN) were still significantly stronger than to PMMA surfaces (0.09 nN) (p < 0.01). The biofilm formed on PET surfaces was also significantly denser and more than on PMMA surfaces (p < 0.05). In conclusion, the bacterial adhesion to PMMA was significantly less in comparison with PET. PMMA may be preferable for patients who have poor oral hygiene, caries susceptibility, periodontosis, and halitosis. SCANNING 38:665-670, 2016. © 2016 Wiley Periodicals, Inc.

  15. Surface hydrophilic modification of acrylonitrile-butadiene-styrene terpolymer by poly(ethylene glycol-co-1,4-cyclohexanedimethanol terephthalate): Preparation, characterization, and properties studies

    NASA Astrophysics Data System (ADS)

    Chen, Tingting; Zhang, Jun

    2016-12-01

    Surface hydrophilic modified acrylonitrile-butadiene-styrene (ABS) terpolymer was prepared by melt blending with poly(ethylene glycol-co-1,4-cyclohexanedimethanol terephthalate) (PETG) random copolymer as the modifier. Attenuated total reflectance-Fourier transform-infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS) were used for surface analysis. Through the contact angle measurement, the relationship between surface properties of the ABS/PETG blends and PETG content was investigated. Scanning electron microscope (SEM) and dynamical mechanical thermal analysis (DMTA) were used to characterize interface morphology and compatibility of the blends. The effect of PETG content on the mechanical and rheological properties was examined. The ATR-FTIR and XPS analysis suggested that the hydrophilic groups were enriched on the surface with increasing PETG content in the blend. The decrease of the water contact angle and the increase of the polarity for the blends with increasing PETG content indicated that the hydrophilic property of the blends was enhanced with increasing PETG content. The ABS/PETG blends were partially miscible. And the blends with ≤50 wt% PETG had better compatibility than the blends with above 50 wt% PETG. It was clear that below 50 wt% PETG, the PETG phase was dispersed in spherical form and the ABS phase was continuous. Above 50 wt% PETG, the PETG phase became continuous and the ABS phase was dispersed in irregular form. Moreover, the tensile strength and flexural strength of the blends were enhanced with increasing PETG content. The flexural modulus almost remained constant. And the impact strength was decreased when the content of PETG was increasing.

  16. 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.

  17. 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.

  18. Modification of amorphous poly(ethylene terephthalate) surface by UV light and plasma for fabrication of an electrophoresis chip with an integrated gold microelectrode.

    PubMed

    Hao, Zhenxia; Chen, Hengwu; Zhu, Xiaoying; Li, Jingmin; Liu, Chong

    2008-10-31

    Amorphous poly(ethylene terephthalate) (PET), which possess a low softening temperature (T(s)=75 degrees C), was exploited to fabricate the electrophoresis chip with an integrated gold electrode for amperometric detection, with emphases being focused on the PET surface modification via UV light and air plasma. Both UV irradiation and plasma treatment were found to be able to improve the surface wettability, enhance the supported electroosmotic flow (EOF), and increase thermal bonding strength of PET sheets, with the latter being more efficient and less time-consuming than the former in the surface modification. Upon treated with plasma for 2 min, the PET sheets could be thermally bonded at 65 degrees C. T-peer test showed that the bonding strength increased from 10 g/cm for native PET sheets to 1250 g/cm for the plasma treated sheets when chips were bonded at the softening point, Attenuated-total-internal-reflection spectrum showed that, after being exposed to the UV light, carboxylic groups site-selectively formed in the UV-exposed region on PET surface. These UV-induced carboxylic groups were further utilized as the scaffold for preparation of micro-gold electrode via electroless gold plating. By using this established UV-directed electroless plating and the plasma-assisted thermal bonding techniques, the full PET electrophoresis chip with an integrated micro-gold electrode could be fabricated in common chemistry laboratory without the need of clean rooms. The fabricated PET chips were demonstrated for separation and detection of model analytes of dopamine (DA) and catechol (CA). Satisfactory resolution of the two analytes was achieved within 40s, and detection limits of 0.87 microM and 1.28 microM for DA and CA were obtained, respectively.

  19. 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.

  20. The effects of mechanical milling and alloying on poly(ethylene terephthalate) and its blends with Vectra(TM) liquid crystalline polymer

    NASA Astrophysics Data System (ADS)

    Bai, Changhe

    Poly(ethylene terephthalate) (PET) has been subjected to high-energy ball-milling (mechanical milling) performed at three different temperatures. The resulting milled powder is characterized by molecular weight measurements, differential scanning calorimetry and wide-angle x-ray scattering. Regardless of the initial degree of crystallinity or milling temperature employed, mechanical milling of PET yields an "oriented amorphous" morphology in which the PET chains are aligned but rotationally disordered, which explains the amorphous wide-angle x-ray pattern from mechanically milled (MM) PET and the small, broad crystallization exotherm. and a large melting endotherm. Evidence is also presented to suggest that extended-chain crystals of PET are produced after crystallization of MM PET. Mechanical alloying of PET and a liquid crystalline polymer VectraTM has been performed at either room temperature or cryogenic temperature. Morphological studies using optical microscopy, TEM, and x-ray microscopy reveal that intimate mixing of PET and Vectra on a sub-micrometer scale has been achieved by mechanical alloying. No prior reports of preparing PET/Vectra blends on such a fine scale have been documented, which shows the efficacy of solid state mixing via mechanical alloying. The milled alloy is thermally unstable and severe phase separation ensues during post thermal processing. The scale of mixing can be largely preserved by compaction at a temperature below the melting point of either constituent polymer, which gives rise to rule-of-mixtures behavior in alloy hardness. Vectra does not function as a nucleation agent for PET, as evidenced from isothermal crystallization. Hot-melt adhesives may be a potential application for MA PET/Vectra blends. The scale of mixing, however, does not correlate with interfacial fracture toughness.

  1. 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

  2. Inactivation of Escherichia coli O157:H7 and Aerobic Microorganisms in Romaine Lettuce Packaged in a Commercial Polyethylene Terephthalate Container Using Atmospheric Cold Plasma.

    PubMed

    Min, Sea C; Roh, Si Hyeon; Boyd, Glenn; Sites, Joseph E; Uknalis, Joseph; Fan, Xuetong; Niemira, Brendan A

    2017-01-01

    The effects of dielectric barrier discharge atmospheric cold plasma (DACP) treatment on the inactivation of Escherichia coli O157:H7 and aerobic microorganisms in romaine lettuce packaged in a conventional commercial plastic container were evaluated during storage at 4°C for 7 days. Effects investigated included the color, carbon dioxide (CO2) generation, weight loss, and surface morphology of the lettuce during storage. Romaine lettuce pieces, with or without inoculation with a cocktail of three strains of E. coli O157:H7 (~6 log CFU/g of lettuce), were packaged in a polyethylene terephthalate commercial clamshell container and treated at 34.8 kV at 1.1 kHz for 5 min by using a DACP treatment system equipped with a pin-type high-voltage electrode. Romaine lettuce samples were analyzed for inactivation of E. coli O157:H7, total mesophilic aerobes, and yeasts and molds, color, CO2 generation, weight loss, and surface morphology during storage at 4°C for 7 days. The DACP treatment reduced the initial counts of E. coli O157:H7 and total aerobic microorganisms by ~1 log CFU/g, with negligible temperature change from 24.5 ± 1.4°C to 26.6 ± 1.7°C. The reductions in the numbers of E. coli O157:H7, total mesophilic aerobes, and yeasts and molds during storage were 0.8 to 1.5, 0.7 to 1.9, and 0.9 to 1.7 log CFU/g, respectively. DACP treatment, however, did not significantly affect the color, CO2 generation, weight, and surface morphology of lettuce during storage (P > 0.05). Some mesophilic aerobic bacteria were sublethally injured by DACP treatment. The results from this study demonstrate the potential of applying DACP as a postpackaging treatment to decontaminate lettuce contained in conventional plastic packages without altering color and leaf respiration during posttreatment cold storage.

  3. 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

  4. 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.

  5. 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}.

  6. 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.

  7. 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.

  8. 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

  9. Structure property relationships in polymer blends and composites. Part I. Polymer/POSS composites. Part II. Poly(ethylene terephthalate) ionomer/polyamide 6 blends. Part III. Elastomer/boron nitride composites

    NASA Astrophysics Data System (ADS)

    Iyer, Subramanian

    Multiphase polymer systems are an increasingly important technical area of polymer science. By definition, a multiphase system is one that has two or more distinct phases. From the standpoint of commercial applications and developments, polymer blending represents one of the easiest ways to achieve properties not available in individual materials. This work discusses the structure property relationships in polymer certain blends and composites. Polymer/polyhedral oligomeric silsesquioxanes (POSSRTM) blends and copolymers have gained significant attention in the last decade due the unique properties of the inorganic-organic hybrid structure of POSS. The majority of the research in polymer/POSS has been in the form of copolymers and thermosets. The criteria for the reinforcement of polymers using POSS as a filler material is not been discussed in literature. Part I of the thesis will highlight the effect of blending POSS with different polymers and discuss the rules for reinforcement of polymers when using POSS as a filler material. Part II of the thesis will discuss the structure property relationships in poly(ethylene terephthalate) ionomer/polyamide 6 blends. Part III will discuss the control of coefficient of thermal expansion of elastomers using boron nitride as a filler material.

  10. The use of layer by layer self-assembled coatings of hyaluronic acid and cationized gelatin to improve the biocompatibility of poly(ethylene terephthalate) artificial ligaments for reconstruction of the anterior cruciate ligament.

    PubMed

    Li, Hong; Chen, Chen; Zhang, Shurong; Jiang, Jia; Tao, Hongyue; Xu, Jialing; Sun, Jianguo; Zhong, Wei; Chen, Shiyi

    2012-11-01

    In this study layer by layer (LBL) self-assembled coatings of hyaluronic acid (HA) and cationized gelatin (CG) were used to modify polyethylene terephthalate (PET) artificial ligament grafts. Changes in the surface properties were characterized by scanning electron microscopy, attenuated total reflection Fourier transform infrared spectroscopy, energy-dispersive X-ray spectroscopy, and contact angle and biomechanical measurements. The cell compatibility of this HA-CG coating was investigated in vitro on PET films seeded with human foreskin dermal fibroblasts over 7days. The results of our in vitro studies demonstrated that the HA-CG coating significantly enhanced cell adhesion, facilitated cell growth, and suppressed the expression of inflammation-related genes relative to a pure PET graft. Furthermore, rabbit and porcine anterior cruciate ligament reconstruction models were used to evaluate the effect of this LBL coating in vivo. The animal experiment results proved that this LBL coating significantly inhibited inflammatory cell infiltration and promoted new ligament tissue regeneration among the graft fibers. In addition, the formation of type I collagen in the HA-CG coating group was much higher than in the control group. Based on these results we conclude that PET grafts coated with HA-CG have considerable potential as substitutes for ligament reconstruction.

  11. 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.

  12. Conducting polymer films fabricated by oxidative graft copolymerization of aniline on poly(acrylic acid) grafted poly(ethylene terephthalate) surfaces.

    PubMed

    Wang, Jiku; Liu, Xuyan; Choi, Ho-Suk; Kim, Jong-Hoon

    2008-11-27

    A conductive polyaniline/poly(ethylene terephthalate) (PANI/PET) composite film was fabricated via the oxidative graft copolymerization of aniline (ANI) onto the plasma-induced poly(acrylic acid) (PAAc) grafted PET surface. The attenuated total reflectance Fourier transform infrared spectroscopy spectra (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS) results confirmed that PANI was successfully grafted onto the surface of the PAAc-g-PET films. The effects of the experimental conditions on the percentage of PANI grafted onto the PAAc-g-PET films were extensively investigated. A very high grafting percentage of ANI can be obtained through the acid-base reaction between the aniline monomer and PAAc on the PAAc-g-PET surface at high temperature. As a result, the grafting percentage of PANI can be increased to as high as 12.18 wt %, which causes the surface resistance of the PANI-g-PAAc-g-PET film to be reduced to about 1000 Omega/sq. We predicted that this is because of the high flexibility of the PAAc molecular chains and high solubility of aniline, both of which facilitate the binding of aniline to PAAc during this high temperature acid-base reaction. It was observed by atomic force microscopy (AFM) that the PANI-modified PET surface exhibits higher size irregularity and surface roughness, which further indicated that a much greater number of aniline molecules can be reactively bonded to and distributed along the grafted AAc chains and that the PANI-g-PAAc-g-PET surface resulting from the sequential oxidative graft copolymerization can possess higher electrical conductivity.

  13. Radiation damage and recovery properties of common plastics PEN (Polyethylene Naphthalate) and PET (Polyethylene Terephthalate) using a 137Cs gamma ray source up to 1.4 Mrad and 14 Mrad

    NASA Astrophysics Data System (ADS)

    Wetzel, J.; Tiras, E.; Bilki, B.; Onel, Y.; Winn, D.

    2016-08-01

    Polyethylene naphthalate (PEN) and polyethylene teraphthalate (PET) are cheap and common polyester plastics used throughout the world in the manufacturing of bottled drinks, containers for foodstuffs, and fibers used in clothing. These plastics are also known organic scintillators with very good scintillation properties. As particle physics experiments increase in energy and particle flux density, so does radiation exposure to detector materials. It is therefore important that scintillators be tested for radiation tolerance at these generally unheard of doses. We tested samples of PEN and PET using laser stimulated emission on separate tiles exposed to 1 Mrad and 10 Mrad gamma rays with a 137Cs source. PEN exposed to 1.4 Mrad and 14 Mrad emit 71.4% and 46.7% of the light of an undamaged tile, respectively, and maximally recover to 85.9% and 79.5% after 5 and 9 days, respectively. PET exposed to 1.4 Mrad and 14 Mrad emit 35.0% and 12.2% light, respectively, and maximally recover to 93.5% and 80.0% after 22 and 60 days, respectively.

  14. 76 FR 50456 - Notice of Final Results of Antidumping Duty Changed Circumstances Review: Polyethylene...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-15

    ...: Polyethylene Terephthalate Film, Sheet, and Strip From the Republic of Korea AGENCY: Import Administration... polyethylene terephthalate film, sheet, and strip (PET film) from Korea, effective as of the date of... Department published an antidumping duty order on PET film from Korea on June 5, 1991. See Antidumping...

  15. 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

  16. 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.

  17. 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.

  18. 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

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

    PubMed

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

    2015-02-04

    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.

  20. Toxicological review and oral risk assessment of terephthalic acid (TPA) and its esters: A category approach.

    PubMed

    Ball, Gwendolyn L; McLellan, Clifton J; Bhat, Virunya S

    2012-01-01

    Polyethylene terephthalate, a copolymer of terephthalic acid (TPA) or dimethyl terephthalate (DMT) with ethylene glycol, has food, beverage, and drinking water contact applications. Di-2-ethylhexyl terephthalate (DEHT) is a plasticizer in food and drinking water contact materials. Oral reference doses (RfDs) and total allowable concentrations (TACs) in drinking water were derived for TPA, DMT, and DEHT. Category RfD and TAC levels were also established for nine C(1)-C(8) terephthalate esters. The mode of action of TPA, and of DMT, which is metabolized to TPA, involves urinary acidosis, altered electrolyte elimination and hypercalciuria, urinary supersaturation with calcium terephthalate or calcium hydrogen terephthalate, and crystallization into bladder calculi. Weanling rats were more sensitive to calculus formation than dams. Calculi-induced irritation led to bladder hyperplasia and tumors in rats fed 1000 mg/kg-day TPA. The lack of effects at 142 mg/kg-day supports a threshold for urine saturation with calcium terephthalate, a key event for calculus formation. Chronic dietary DMT exposure in rodents caused kidney inflammation, but not calculi. Chronic dietary DEHT exposure caused general toxicity unrelated to calculi, although urine pH was reduced suggesting the TPA metabolite was biologically-active, but of insufficient concentration to induce calculi. Respective oral reference doses of 0.5, 0.5, and 0.2 mg/kg-day and total allowable drinking water concentrations of 3, 3, and 1 mg/L were derived for TPA, DMT, and DEHT. An oral RfD of 0.2 mg/kg-day for the terephthalate category chemicals corresponded to a drinking water TAC of 1 mg/L.

  1. 21 CFR 177.1660 - Poly (tetramethylene terephthalate).

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... (tetramethylene terephthalate) is the reaction product of dimethyl terephthalate with 1,4-butanediol to which may... in phenol/tetrachloroethane (60/40 weight ratio) solvent is not less than 0.6 as determined using...

  2. 21 CFR 177.1660 - Poly (tetramethylene terephthalate).

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... (tetramethylene terephthalate) is the reaction product of dimethyl terephthalate with 1,4-butanediol to which may... in phenol/tetrachloroethane (60/40 weight ratio) solvent is not less than 0.6 as determined using...

  3. Renal handling of terephthalic acid

    SciTech Connect

    Tremaine, L.M.; Quebbemann, A.J.

    1985-01-01

    By use of the Sperber in vivo chicken preparation method, infusion of radiolabeled terephthalic acid ((/sup 14/C)TPA) into the renal portal circulation revealed a first-pass excretion of the unchanged compound into the urine. This model was utilized further to characterize the excretory transport of (/sup 14/C)TPA and provide information on the structural specificity in the secretion of dicarboxylic acids. At an infusion rate of 0.4 nmol/min. 60% of the (/sup 14/C)TPA which reached the kidney was directly excreted. An infusion rate of 3 or 6 mumol/min resulted in complete removal of (/sup 14/C)TPA by the kidney. These results indicate that TPA is both actively secreted and actively reabsorbed when infused at 0.4 nmol/min and that active reabsorption is saturated with the infusion of TPA at higher concentrations. The secretory process was saturated with the infusion of TPA at 40 mumol/mn. The excretory transport of TPA was inhibited by the infusion of probenecid, salicylate, and m-hydroxybenzoic acid, indicating that these organic acids share the same organic anion excretory transport process. m-Hydroxybenzoic acid did not alter the simultaneously measured excretory transport of p-aminohippuric acid (PAH), suggesting that there are different systems involved in the secretion of TPA and PAH. The structural specificity for renal secretion of dicarboxylic acids was revealed by the use of o-phthalic acid and m-phthalic acid as possible inhibitors of TPA secretion.

  4. Enzymatic hydrolysis of poly(ethylene furanoate).

    PubMed

    Pellis, Alessandro; Haernvall, Karolina; Pichler, Christian M; Ghazaryan, Gagik; Breinbauer, Rolf; Guebitz, Georg M

    2016-10-10

    The urgency of producing new environmentally-friendly polyesters strongly enhanced the development of bio-based poly(ethylene furanoate) (PEF) as an alternative to plastics like poly(ethylene terephthalate) (PET) for applications that include food packaging, personal and home care containers and thermoforming equipment. In this study, PEF powders of various molecular weights (6, 10 and 40kDa) were synthetized and their susceptibility to enzymatic hydrolysis was investigated for the first time. According to LC/TOF-MS analysis, cutinase 1 from Thermobifida cellulosilytica liberated both 2,5-furandicarboxylic acid and oligomers of up to DP4. The enzyme preferentially hydrolyzed PEF with higher molecular weights but was active on all tested substrates. Mild enzymatic hydrolysis of PEF has a potential both for surface functionalization and monomers recycling.

  5. 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. ...

  6. Acute Inhalation Toxicity of Pyrotechnically Disseminated Terephthalic Acid

    DTIC Science & Technology

    1988-07-01

    calcium concentrations in the bladder, followed by urolithiasis with irritation induced hyperplasia and neoplasms. However, these effects only occur...R.W., Popp, J.A., Heck, H., "Chemical Urolithiasis , 1. Characteristics of Bladder Stone Induction by Terephthalic Acid and Dimethyl Terephthalate in

  7. Development of biodegradable metaloxide/polymer nanocomposite films based on poly-ε-caprolactone and terephthalic acid.

    PubMed

    Varaprasad, Kokkarachedu; Pariguana, Manuel; Raghavendra, Gownolla Malegowd; Jayaramudu, Tippabattini; Sadiku, Emmanuel Rotimi

    2017-01-01

    The present investigation describes the development of metal-oxide polymer nanocomposite films from biodegradable poly-ε-caprolactone, disposed poly(ethylene terephthalate) oil bottles monomer and zinc oxide-copper oxide nanoparticles. The terephthalic acid and zinc oxide-copper oxide nanoparticles were synthesized by using a temperature-dependent precipitation technique and double precipitation method, respectively. The terephthalic acid synthesized was confirmed by FTIR analysis and furthermore, it was characterized by thermal analysis. The as-prepared CuO-ZnO nanoparticles structure was confirmed by XRD analysis and its morphology was analyzed by SEM/EDS and TEM. Furthermore, the metal-oxide polymer nanocomposite films have excellent mechanical properties, with tensile strength and modulus better than pure films. The metal-oxide polymer nanocomposite films that were successfully developed show a relatively brighter colour when compared to CuO film. These new metal-oxide polymer nanocomposite films can replace many non-degradable plastics. The new metal-oxide polymer nanocomposite films developed are envisaged to be suitable for use in industrial and domestic packaging applications.

  8. 21 CFR 177.1660 - Poly (tetramethylene terephthalate).

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... reaction product of dimethyl terephthalate with 1,4-butanediol to which may have been added certain... part. (c) Specifications. (1) Inherent viscosity of a 0.50 percent solution of the polymer in...

  9. 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.

  10. 21 CFR 177.1660 - Poly (tetra-methylene tereph-thalate).

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ..., poly (tetramethylene terephthalate) is the reaction product of dimethyl terephthalate with 1,4... percent solution of the polymer in phenol/tetrachloroethane (60/40 weight ratio) solvent is not less...

  11. 21 CFR 177.1660 - Poly (tetra-methyl-ene tere-phtha-late).

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... (tetramethylene terephthalate) is the reaction product of dimethyl terephthalate with 1,4-butanediol to which may... in phenol/tetrachloroethane (60/40 weight ratio) solvent is not less than 0.6 as determined using...

  12. 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

  13. 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

    ... factors of production (``FOP'') valued in a surrogate market-economy country or countries considered... using ``to the extent possible, the prices or costs of factors of production in one or more market.... Specifically, `` * * * if more than one country has survived the selection process to this point, the...

  14. 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.

  15. 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.

  16. 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

    ..., 2011 (``Wanhua Report''). Non-Market Economy Country Status The Department has treated the PRC as a non-market economy (``NME'') country in all past antidumping duty investigations and administrative reviews and continues to do so in this case.\\12\\ The Department has previously examined the PRC's...

  17. 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.

  18. 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.

  19. 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

    ... calculated surrogate overhead, selling, general and administrative expenses, and profit applicable to... of merchandise comparable to subject merchandise; \\9\\ (2) revised the surrogate value for bright polyester chips and master batch chips by using the simple-average of the two weighted average...

  20. 75 FR 81574 - Polyethylene Terephthalate Film, Sheet, and Strip From India: Preliminary Results of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-28

    ...\\ SRF Original Response of June 10, 2010 (QR-SRF), at Exhibits 9(a)(i-ii). Benchmark Interest Rates and... Original Response of May 27, 2010 (QR-GOI), at 19. In the 2005 administrative review of this proceeding... from those specified in the original license. \\5\\ See QR-SRF, at 65-66, and Exhibits 31(a)-(c). \\6\\...

  1. Determination of benzene residues in recycled polyethylene terephthalate (PETE) by dynamic headspace-gas chromatography.

    PubMed

    Komolprasert, V; Hargraves, W A; Armstrong, D J

    1994-01-01

    A dynamic headspace-gas chromatography (HS/GC) method was developed to quantitate benzene in recycled PETE material derived from 21 PETE beverage bottles. The analytical system consisted of a purge-and-trap apparatus which was interfaced directly with a gas chromatograph/flame ionization detector. Cryofocusing and non-cryofocusing GC systems were used. The technique was applied to spiked PETE test samples which were prepared at various benzene concentrations ranging from 100 ppb to 117 ppm. The initial spiked benzene concentration in the PETE test samples was determined gravimetrically. The HS/GC technique was limited by the slow desorption rate of benzene from the PETE matrix; as a result, multipurges were performed at 60 degrees C. Regression analysis was done on the multipurge data to develop a desorption model which would predict the total amount of benzene in the PETE. The calculated results agreed with the experimental recoveries within +/- 10%. Recovery depended on the initial benzene level in the PETE and ranged from 70 to 90% after the first five purges.

  2. 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

    ..., through October 31, 2012. The review covers two mandatory respondents (Shaoxing Xiangyu Green Packing Co... for the POR: Weighted- average Exporter dumping margin (percent) Shaoxing Xiangyu Green Packing Co... the record.\\9\\ Furthermore, the Department generally will not accept business proprietary...

  3. 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

    ..., and strip (``PET film'') from the People's Republic of China (``PRC'').\\1\\ The period of review (``POR... administrative review of PET film from the People's Republic of China.\\2\\ On November 28, 2011, DuPont Teijin... raw, pre- treated, or primed PET film, whether extruded or co-extruded. Excluded are metalized...

  4. 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

    ... failed to cooperate to the best of its ability in this proceeding by refusing to respond to the... the Department's disposal. Secondary information is described as `` nformation derived from the... Department will consider information reasonably at its disposal to determine whether a margin continues...

  5. 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

    .... The Department preliminarily determines that SRF did, and that Jindal did not, make sales of subject...\\ However, where the respondent did not report the entered value for its sales, we will calculate...

  6. 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

    ...: 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 the... content. Changes Since the Preliminary Results Based on our analysis of the comments received, we did...

  7. 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

    ... exporter of PET Film from India. The Department preliminarily determines that Ester did not make sales of..., Ester provided a chart of its selling functions.\\2\\ However, it did not provide a breakout of sales... chart to include the level of degree of the selling activities, but did not break out the...

  8. 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

    ... value (NV), we compared Kolon's constructed export price (CEP) or export price (EP) sales made in the United States to unaffiliated purchasers to NV, as described in the ``United States Price'' and ``Normal... ordinary course of trade in the home market to compare to a U.S. sale, we compared the price of the...

  9. 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

    ...-Length Carbon Steel Plate from Romania: Initiation and Preliminary Results of Changed Circumstances Antidumping Duty Administrative Review, 70 FR 22847 (May 3, 2005) (Plate from Romania), unchanged in Notice of... from Romania 70 FR 35624 (June 21, 2005). While no single factor or combination of factors...

  10. 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.

  11. 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.

  12. Thermal Properties and Morphological Analyses of poly(ethylene terephthalate)[PET] Solid State Polymerized

    NASA Astrophysics Data System (ADS)

    Medellin-Rodriguez, F. J.; Lopez-Guillen, R.

    1997-03-01

    High molecular weight PET was obtained through solid state polymerization of commercial PET. After optimizing synthesis variables such as time and reaction temperature, catalyst and gas flow rate, bulk crystallization studies were made with the products in terms of crystallization time and temperature. Molecular crystallization analyses were then performed for the highest molecular weight PET and also for the commercial reference. Isothermal crystallization and melting experiments were systematically practiced in order to characterize the high molecular weight PET. Bulk crystallization studies indicated changes in nucleation patterns from instantaneous to sporadic as the molecular weight was increased. When the molecular crystallization results were correlated with secondary nucleation theory and Regime III, a proportional relationship between the elementary jump activation energy and molecular weight was found. Melting experiments indicated that the main effect of increasing molecular weight is an increase in the second melting endotherm when this feature is present. The support by CONACyT through grant No. 0667P-A is greatly appreciated.

  13. 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.

  14. 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

    ... Commission defined a single Domestic Like Product coextensive with Commerce's scope. (4) The Domestic... the product. In its original determinations, the Commission defined a single Domestic Industry... person or firm engaged, either directly or through a parent company or subsidiary, in importing...

  15. 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.

  16. 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 ...

  17. 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,...

  18. 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,...

  19. 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,...

  20. Heat capacity of poly(trimethylene terephthalate)

    SciTech Connect

    Pyda, M.; Boller, A.; Wunderlich, B. |; Grebowicz, J.; Chuah, H.

    1997-12-01

    Thermal analysis of poly(trimethylene terephthalate) (PTT) has been carried out using standard differential scanning calorimetry and temperature-modulated differential scanning calorimetry. Heat capacities of the solid and liquid states of semicrystalline PTT are reported from 190 K to 570 K. The semicrystalline PTT has a glass transition temperature of about 331 K. Between 460 K and 480 K, PTT shows an exothermic ordering. The melting endotherm occurs between 480 K and 505 K with an onset temperature of 489.15 K (216 C). The heat of fusion of typical semicrystalline samples is 13.8 kJ/mol. For 100% crystalline PTT the heat of fusion is estimated to be 28--30 kJ/mol. The heat capacity of solid PTT is linked to an approximate group vibrational spectrum, and the Tarasov equation is used to estimate the skeletal vibrational heat capacity ({Theta}{sub 1} = 542 K and {Theta}{sub 3} = 42 K). A comparison of calculation and experimental heat capacities show agreement of better than {+-}2% between 190--300 K. The experimental heat capacity of liquid PTT can be expressed as a linear function of temperature: C{sub p} {sup L}(exp) = 211.6 + 0.434 T J/(K mol) and compares well with estimations from the ATHAS data bank using group contributions of other polymers with the same constituent groups ({+-} 0.5%). The change of heat capacity at T{sub g} of amorphous PTT has been estimated from the heat capacities of liquid and solid to be 86.4 J/(K mol). Knowing C{sub p} of the solid, liquid, and the transition parameters, the thermodynamic functions: enthalpy, entropy and Gibbs function were obtained.

  1. 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.

  2. Cellular polyethylene-naphthalate ferroelectrets: Foaming in supercritical carbon dioxide, structural and electrical preparation, and resulting piezoelectricity

    NASA Astrophysics Data System (ADS)

    Fang, P.; Wegener, M.; Wirges, W.; Gerhard, R.; Zirkel, L.

    2007-05-01

    Polymer foams with electrically charged cellular voids, the so-called ferroelectrets, are soft piezoelectric transducer materials. Several polymers such as polyethylene terephthalate or cyclo-olefin copolymers are under investigation with respect to their suitability as ferroelectrets. Here, the authors report an additional ferroelectret polymer, cellular polyethylene-naphthalate (PEN), which was prepared from commercial uniform polymer films by means of foaming in supercritical carbon dioxide, inflation, biaxial stretching, electrical charging, and metallization. Piezoelectric d33 coefficients of up to 140pC/N demonstrate the suitability of such cellular PEN films for transducer applications. Their piezoelectricity is partially stable at elevated temperatures as high as 100°C.

  3. 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.

  4. [Biodegradation of polyethylene].

    PubMed

    Yang, Jun; Song, Yi-ling; Qin, Xiao-yan

    2007-05-01

    Plastic material is one of the most serious solid wastes pollution. More than 40 million tons of plastics produced each year are discarded into environment. Plastics accumulated in the environment is highly resistant to biodegradation and not be able to take part in substance recycle. To increase the biodegradation efficiency of plastics by different means is the main research direction. This article reviewed the recent research works of polyethylene biodegradation that included the modification and pretreatment of polyethylene, biodegradation pathway, the relevant microbes and enzymes and the changes of physical, chemical and biological properties after biodegradation. The study directions of exploiting the kinds of life-forms of biodegradation polyethylene except the microorganisms, isolating and cloning the key enzymes and gene that could produce active groups, and enhancing the study on polyethylene biodegradation without additive were proposed.

  5. 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).

  6. Gas Diffusion in Polyethylene Terepthalate By Molecular Dynamics

    NASA Astrophysics Data System (ADS)

    Butler, Simon; Adolf, David

    2006-03-01

    Molecular dynamics simulations of the diffusion of small penetrants through PET have been performed utilising the anisotropic united atom model [1] and a virtual liquid technique. [2] The accuracy and reliability of these two approaches has been assessed in terms of the improvement in equation of state behaviour and of diffusion co-efficients and solubilities. The effect of the diffusion of nitrogen, carbon dioxide, and oxygen on the local dynamics of PET have been investigated as a result. Attention has been focused on the dual mode effect [3] observed during mixed gas diffusion. [1] Molecular dynamics calculation of the equation of state of alkanes, J. Chem. Phys. 93, 6 (1990) [2] Kikuchi, Kuwajima, Fukada, Novel method to estimate the solubility of small molecules in cis-polyisoprene by molecular dynamics simulations, J. Chem. Phys, 115, 13 (2001) [3] Lewis, Duckett, Ward, Fairclough, Ryan, The barrier properties of polyethylene terephthalate to mixtures of oxygen, carbon dioxide and nitrogen, Polymer, 1631, 44 (2003)

  7. A Sustainable Route to a Terephthalic Acid Precursor.

    PubMed

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

    2016-05-10

    A new synthetic pathway for the production of p-toluic acid has been developed starting from reagents derived from renewable resources. A Diels-Alder reaction between sorbic and acrylic acids is followed by a combined dehydrogenation/ decarboxylation process, providing p-toluic acid in high yields. This route permits to use milder conditions compared to other Diels-Alder approaches reported in the literature, and therefore can contribute to a more sustainable terephthalic acid production.

  8. 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.

  9. 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.

  10. 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... CONSUMPTION Coatings, Films and Related Substances § 172.260 Oxidized polyethylene. Oxidized polyethylene may... polyethylene is the basic resin produced by the mild air oxidation of polyethylene. The polyethylene used...

  11. 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... CONSUMPTION Coatings, Films and Related Substances § 172.260 Oxidized polyethylene. Oxidized polyethylene may... polyethylene is the basic resin produced by the mild air oxidation of polyethylene. The polyethylene used...

  12. 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... CONSUMPTION Coatings, Films and Related Substances § 172.260 Oxidized polyethylene. Oxidized polyethylene may... polyethylene is the basic resin produced by the mild air oxidation of polyethylene. The polyethylene used...

  13. 21 CFR 177.1345 - Ethylene/1,3-phenylene oxyethylene isophthalate/ terephthalate copolymer.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ethylene/1,3-phenylene oxyethylene isophthalate... Components of Single and Repeated Use Food Contact Surfaces § 177.1345 Ethylene/1,3-phenylene oxyethylene isophthalate/ terephthalate copolymer. Ethylene/1,3-phenylene oxyethylene isophthalate/terephthalate...

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

    PubMed

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

    2014-05-07

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

  15. 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.

  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. 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.

  18. Nanofibers drawing and nanodevices assembly in poly(trimethylene terephthalate).

    PubMed

    Xing, Xiaobo; Wang, Yuqing; Li, Baojun

    2008-07-07

    We report flexible and elastic enough nanofibers with diameters down to 60 nm and lengths up to 500 mm, fabricated by one-step drawing process from molten poly(trimethylene terephthalate) (PTT), exhibiting high surface smoothness and length uniformity. A series of ultracompact devices (such as optical beam splitters, couplers, rings, resonators, and tweezer/scissor-shaped structures) and nanophotonic device arrays have been assembled by the PTT nanofibers. Quantitative studies demonstrate that the PTT nanofibers/nanofiber devices exhibit good guiding properties with low optical loss from visible to near infrared region. The results suggest that the PTT nanophotonic fibers/wires would be promising candidates in constructing miniaturized photonic devices and ultracompact photonic integrated circuits (PICs), and a one-step drawing as an alternative to the standard optical bench technique.

  19. 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.

  20. 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... § 172.260 Oxidized polyethylene. Oxidized polyethylene may be safely used as a component of food, subject to the following restrictions: (a) Oxidized polyethylene is the basic resin produced by the...

  1. 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...

  2. 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...

  3. 21 CFR 172.260 - Oxidized polyethylene.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Oxidized polyethylene. 172.260 Section 172.260 Food... Coatings, Films and Related Substances § 172.260 Oxidized polyethylene. Oxidized polyethylene may be safely used as a component of food, subject to the following restrictions: (a) Oxidized polyethylene is...

  4. Ethylenediammonium dication: H-bonded complexes with terephthalate, chloroacetate, phosphite, selenite and sulfamate anions. Detailed vibrational spectroscopic and theoretical studies of ethylenediammonium terephthalate.

    PubMed

    Marchewka, M K; Drozd, M

    2012-12-01

    Crystalline complexes between ethylenediammonium dication and terephthalate, chloroacetate, phosphite, selenite and sulfamate anions were obtained by slow evaporation from water solution method. Room temperature powder infrared and Raman measurements were carried out. For ethylenediammonium terephthalate theoretical calculations of structure were performed by two ways: ab-initio HF and semiempirical PM3. In this case the PM3 method gave more accurate structure (closer to X-ray results). The additional PM3 calculations of vibrational spectra were performed. On the basis theoretical approach and earlier vibrational studies of similar compounds the vibrational assignments for observed bands have been proposed. All compounds were checked for second harmonic generation (SHG).

  5. 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.

  6. Reaction in the Melt of Post-consumer Poly(ethylene terephthalate) (PET) with Ester Functionalized Polyolefins

    NASA Astrophysics Data System (ADS)

    Coltelli, Maria-Beatrice; Savi, Stefania; Aglietto, Mauro; Ciardelli, Francesco

    2010-06-01

    The blending of PET from post-consumer packaging products with polyolefins can provide toughened materials. PET and polyolefins are immiscible polymers and to the above purpose, different method of reactive compatibilization are investigated to achieve a fine dispersion of polyolefin domains into a PET matrix. The use of a functionalized polyolefin, bearing reactive groups toward PET terminals, is a promising route to obtain grafted copolymers acting as interface stabilizers. In particular the use in the melt blending of ester or hydroxyl functionalized polyolefins in the presence of transesterification catalysts and or anhydride functionalized polyolefins as compatibilizer precursors were both investigated by focusing onto the relevant chemical aspects. The prepared blends were analyzed through suitable fractionation methods, such as selective extractions, and spectroscopic analysis in order to identify the molecular architecture of the PET-polyolefin copolymers macromolecules resulting from the process and study their effectiveness at the interface region. Moreover the phase morphology and the thermo-mechanical properties were investigated and correlated to structure of the macromolecular species in the system.

  7. 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

    ... of China: Notice of Court Decision Not in Harmony With Final Results of Administrative Review and... Sawblades''), the Department is notifying the public that the final judgment in this case is not in harmony...: Notice of Court Decision Not in Harmony With Final Results of Administrative Review and Notice of...

  8. 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.

  9. 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.

  10. 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

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF COMMERCE...: Import Administration, International Trade Administration, Department of Commerce. SUMMARY: On September 1, 2010, the Department of Commerce (the Department) initiated the third sunset review of...

  11. 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

    ...., Ltd. v. United States, Slip Op. 13-10 (CIT 2013).\\1\\ \\1\\ See Final Results of Redetermination Pursuant.../remands (``PET Film Final Remand''); see also Fuwei Films (Shandong) Co., Ltd. v. United States, Consol... decision of the United States Court of Appeals for the Federal Circuit (``CAFC'') in Timken Co. v....

  12. 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.

  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. 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.

  15. 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

  16. Effects of compatibilization on the essential work of fracture parameters of in situ microfiber reinforced poly(ethylene terephtahalate)/polyethylene blend

    SciTech Connect

    Li Zhongming; Yang Wei; Xie Banghu; Yang, S.Y.; Yang Mingbo; Feng Jianmin; Huang Rui

    2003-11-26

    A novel in situ microfiber reinforced blend (MRB) based on poly(ethylene terephthalate) (PET) and polyethylene (PE) was prepared by extrusion-hot stretching-quenching process, and was compatibilized with ethylene vinyl acetate copolymer (EVA) in the presence of the transesterification reaction catalyst, dibutyltin oxide (DBTO). The effects of compatibilization on the essential work of fracture parameters in PET/PE MRB were examined. It is found that the specific essential work of fracture (w{sub e}) and the specific non-essential work of fracture (w{sub p}) were significantly increased, when adding 1 and 2.5 phr of EVA to PET/PE MRB and it was further increased with the addition of 0.5 phr of DBTO as the catalyst of the transesterification reaction. The fracture surfaces study by scanning electron microscope (SEM) further proved that EVA is a successful compatibilizer for PET/PP blend. The morphology study of the blends shows that the well-defined fibers with the diameter of several microns were generated in situ during melt extrusion-hot stretch-quenching processing.

  17. 21 CFR 177.1345 - Ethylene/1,3-phenylene oxyethylene iso-phtha-late/ tere-phtha-late copolymer.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ethylene/1,3-phenylene oxyethylene iso-phtha-late... § 177.1345 Ethylene/1,3-phenylene oxyethylene iso-phtha-late/ tere-phtha-late copolymer. Ethylene/1, 3..., ethylene/1,3-phenylene oxyethylene isophthalate/terephthalate copolymer consists of the basic...

  18. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene, chlorinated. 177.1610 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1610 Polyethylene, chlorinated. Chlorinated polyethylene identified in this section may be safely used as articles or components of articles that...

  19. 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...

  20. 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...

  1. 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...

  2. 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,...

  3. 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... 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...

  4. 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... 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...

  5. 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...

  6. 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...

  7. 76 FR 70896 - Polyethylene Glycol; Tolerance Exemption

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-16

    ... AGENCY 40 CFR Part 180 Polyethylene Glycol; Tolerance Exemption AGENCY: Environmental Protection Agency... amu), 17,000; also known as polyethylene glycol, when used as an inert ingredient in a pesticide...(oxyethylene, minimum number average molecular weight (in amu), 17,000; also known as polyethylene...

  8. 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... 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,...

  9. 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,...

  10. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene, chlorinated. 177.1610 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1610 Polyethylene, chlorinated. Chlorinated polyethylene identified in this section may be safely used as articles or components of articles that...

  11. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene, chlorinated. 177.1610 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1610 Polyethylene, chlorinated. Chlorinated polyethylene identified in this section may be safely used as articles or components of articles that...

  12. 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... 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,...

  13. 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... 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,...

  14. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene, chlorinated. 177.1610 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1610 Polyethylene, chlorinated. Chlorinated polyethylene identified in this section may be safely used as articles or components of articles that...

  15. 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...

  16. 21 CFR 177.1345 - Ethylene/1,3-phenylene oxyethylene isophthalate/ terephthalate copolymer.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ethylene/1,3-phenylene oxyethylene isophthalate... Ethylene/1,3-phenylene oxyethylene isophthalate/ terephthalate copolymer. Ethylene/1, 3-phenylene... polymers complying with § 177.1630. (a) Identity. For the purpose of this section,...

  17. 21 CFR 177.1345 - Ethylene/1,3-phenylene oxyethylene isophthalate/ terephthalate copolymer.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ethylene/1,3-phenylene oxyethylene isophthalate... Ethylene/1,3-phenylene oxyethylene isophthalate/ terephthalate copolymer. Ethylene/1, 3-phenylene... polymers complying with § 177.1630. (a) Identity. For the purpose of this section,...

  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... Ethylene/1,3-phenylene oxyethylene isophthalate/ terephthalate copolymer. Ethylene/1, 3-phenylene... polymers complying with § 177.1630. (a) Identity. For the purpose of this section,...

  19. 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.

  20. Determination of Young's modulus of epoxy coated polyethylene micro-cantilever using phase-shift shadow moiré method

    NASA Astrophysics Data System (ADS)

    Lim, J. H.; Ratnam, M. M.; Azid, I. A.; Mutharasu, D.

    2011-11-01

    Young's moduli of various epoxy coated polyethylene terephthalate (PET) micro-cantilevers were determined from the deflection results obtained using the phase-shift shadow moiré (PSSM) method. The filler materials for epoxy coatings were aluminum and graphite powders that were mixed with epoxy at various percentages. Young's moduli were calculated from theory based on the deflection results. The PET micro-cantilever coated with aluminum-epoxy coating showed increasing value of Young's modulus when the ratios of the aluminum-epoxy were increased. The graphite-epoxy coating on the PET micro-cantilever also showed the same trend. The experimental results also show that Young's modulus of the graphite-epoxy coating is higher than aluminum-epoxy coating in comparison at the same mixing ratio.

  1. Raman spectroscopy of biomedical polyethylenes.

    PubMed

    Pezzotti, Giuseppe

    2017-03-27

    With the development of three-dimensional Raman algorithms for local mapping of oxidation and plastic strain, and the ability to resolve molecular orientation patterns with microscopic spatial resolution, there is an opportunity to re-examine many of the foundations on which our understanding of biomedical grade ultra-high molecular weight polyethylenes (UHMWPEs) are based. By implementing polarized Raman spectroscopy into an automatized tool with an improved precision in non-destructively resolving Euler angles, oxidation levels, and microscopic strain, we become capable to make accurate and traceable measurements of the in vitro and in vivo tribological responses of a variety of commercially available UHMWPE bearings for artificial hip and knee joints. In this paper, we first review the foundations and the main algorithms for Raman analyses of oxidation and strain of biomedical polyethylene. Then, we critically re-examine a large body of Raman data previously collected on different polyethylene joint components after in vitro testing or in vivo service, in order to shed new light on an area of particular importance to joint orthopedics: the microscopic nature of UHMWPE surface degradation in the human body. A complex scenario of physical chemistry appears from the Raman analyses, which highlights the importance of molecular-scale phenomena besides mere microstructural changes. The availability of the Raman microscopic probe for visualizing oxidation patterns unveiled striking findings related to the chemical contribution to wear degradation: chain-breaking and subsequent formation of carboxylic acid sites preferentially occur in correspondence of third-phase regions, and they are triggered by emission of dehydroxylated oxygen from ceramic oxide counterparts. These findings profoundly differ from more popular (and simplistic) notions of mechanistic tribology adopted in analyzing joint simulator data.

  2. 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.

  3. Shock induced dissociation of polyethylene

    SciTech Connect

    Morris, C.E.; Loughran, E.D.; Mortensen, G.F.; Gray, G.T. III; Shaw, M.S.

    1989-01-01

    To identify the physical processes occurring on the Hugoniot, shock-recovery experiments were performed. Cylindrical recovery systems were used that enabled a wide range of single-shock Hugoniot states to be examined. Mass spectroscopy was used to examine the gaseous dissociation products. X-ray and TEM measurements were made to characterize the post-shock carbon structures. A dissociation product equation of state is presented to interpret the observed results. Polyethylene (PE) samples that were multiply shocked to their final states dissociated at much higher pressures than single-shocked samples. 5 refs., 2 figs., 1 tab.

  4. 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.

  5. Dynamics in entangled polyethylene melts

    NASA Astrophysics Data System (ADS)

    Salerno, K. Michael; Agrawal, Anupriya; Peters, Brandon L.; Perahia, Dvora; Grest, Gary S.

    2016-10-01

    Polymer dynamics creates distinctive viscoelastic behavior as a result of a coupled interplay of motion at the atomic length scale and motion of the entire macromolecule. Capturing the broad time and length scales of polymeric motion however, remains a challenge. Using linear polyethylene as a model system, we probe the effects of the degree of coarse graining on polymer dynamics. Coarse-grained (CG) potentials are derived using iterative Boltzmann inversion with λ methylene groups per CG bead (denoted CGλ) with λ = 2,3,4 and 6 from a fully-atomistic polyethylene melt simulation. By rescaling time in the CG models by a factor α, the chain mobility for the atomistic and CG models match. We show that independent of the degree of coarse graining, all measured static and dynamic properties are essentially the same once the dynamic scaling factor α and a non-crossing constraint for the CG6 model are included. The speedup of the CG4 model is about 3 times that of the CG3 model and is comparable to that of the CG6 model. Using these CG models we were able to reach times of over 500 μs, allowing us to measure a number of quantities, including the stress relaxation function, plateau modulus and shear viscosity, and compare directly to experiment.

  6. Diffusion of limonene in polyethylene.

    PubMed

    Limm, W; Begley, T H; Lickly, T; Hentges, S G

    2006-07-01

    Diffusion coefficients of limonene in various linear low-density polyethylene (LLDPE) and low-density polyethylene (LDPE) resins have been determined from sorption data using a thermogravimetric methodology. From these data, one can determine whether polymer synthesis parameters such as the choice of catalytic process or co-monomer result in substantial differences in how much food packaging additives might migrate to food. For example, LLDPE is currently manufactured using either one of two distinct catalytic processes: Ziegler-Natta (ZN) and metallocene, a single-site catalyst. ZN catalysis is a heterogeneous process that has dominated polyolefin synthesis over the last half-century. It involves a transition metal compound containing a metal-carbon bond that can handle repeated insertion of olefin units. In contrast, metallocene catalysis has fewer than 20 years of history, but has generated much interest due to its ability to produce highly stereospecific polymers at a very high yield. In addition to high stereospecificity, metallocene-catalysed polymers are significantly lower in polydispersity than traditional ZN counterparts. Absorption and desorption testing of heat-pressed films made from LLDPE and LDPE resins of varying processing parameters indicates that diffusion coefficients of limonene in these resins do not change substantially.

  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. 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.

  9. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... chlorinated polyethylene contains a maximum of 60 percent by weight of total chlorine, as determined by ASTM 1method D1303-55 (Reapproved 1979), “Standard Test Method for Total Chlorine in Vinyl Chloride...

  10. Structure and properties of radiation modified polyethylene

    NASA Astrophysics Data System (ADS)

    Ancharova, U. V.; Mikhailenko, M. A.; Sharafutdinov, M. R.; Tolochko, B. P.; Gerasimov, K. B.; Korobeynikov, M. V.; Bryazgin, A. A.

    2017-01-01

    Polyethylene was irradiated with intensive electron beam with different doses. Structure changes after irradiation ex situ and in situ during heating up to its melting point were studied using synchrotron radiation X-Ray diffraction and thermal analysis.

  11. Reuse of polyethylene waste in road construction.

    PubMed

    Raju, S S S V Gopala; Murali, M; Rengaraju, V R

    2007-01-01

    The cost of construction of flexible pavements depends on thickness of the pavement layers. The thickness of pavement mainly depends on the strength of the subgrade. By suitable improvement to the strength of the subgrade, considerable saving in the scarce resources and economy can be achieved. Because of their lightweight, easy handling, non-breakable and corrosion free nature, polyethylene have surpassed all other materials in utility. But polyethylene waste has been a matter of concern to environmentalists as it is non-biodegradable. In this investigation, an attempt has been made to study the improvement of California Bearing Ratio (CBR) value of soils stabilized with waste polyethylene bags. This alternative material is mixed in different proportions to the gravel and clay to determine the improvement ofCBR value. Use of the waste polyethylene bags observed to have a significant impact on the strength and economy in pavement construction, when these are available locally in large quantities.

  12. Safety and durability of low-density polyethylene bags in solar water disinfection applications.

    PubMed

    Danwittayakul, Supamas; Songngam, Supachai; Fhulua, Tipawan; Muangkasem, Panida; Sukkasi, Sittha

    2016-10-19

    Solar water disinfection (SODIS) is a simple point-of-use process that uses sunlight to disinfect water for drinking. Polyethylene terephthalate (PET) bottles are typically used as water containers for SODIS, but a new SODIS container design has recently been developed with low-density polyethylene (LDPE) bags and can overcome the drawbacks of PET bottles. Two nesting layers of LDPE bags are used in the new design: the inner layer containing the water to be disinfected and the outer one creating air insulation to minimize heat loss from the water to the surroundings. This work investigated the degradation of LDPE bags used in the new design in actual SODIS conditions over a period of 12 weeks. The degradation of the LDPE bags was investigated weekly using a scanning electron microscope, Fourier transform infrared spectroscopy, ultraviolet-visible spectrophotometer, and tensile strength tester. It was found that the LDPE bags gradually degraded under the sunlight due to photo-oxidation reactions, especially in the outer bags, which were directly exposed to the sun and surroundings, leading to the reduction of light transmittance (by 11% at 300 nm) and tensile strength (by 33%). In addition, possible leaching of organic compounds into the water contained in the inner bags was examined using gas chromatography-mass spectrometer. 2,4-Di-tert-butylphenol was found in some SODIS water samples as well as the as-received water samples, in the concentration range of 1-4 μg/L, which passes the Environmental Protection Agency Drinking Water Guidance on Disinfection By-Products.

  13. Radiation resistivity of polyacenaphthylene-grafted polyethylene

    NASA Astrophysics Data System (ADS)

    Hayakawa, Kiyoshi; Kawase, Kaoru; Yamakita, Hiromi

    Thin poly (ethylene-g-acenaphthylene) films prepared by the vapor-phase grafting method were subjected to the γ-irradiation in air, and various changes in tensile and structural properties of the film were investigated by comparing with those of the untreated or crosslinked polyethylene film. Polyethylene got to lose its inherent necking property by oxidative degradation and to be brittle-fractured by the irradiation dose less than 100 Mrad in air. The polyacenaphthylene-grafted polyethylenes (extent of grafting, ˜ 54 by {100( P-P°) }/{P°}), however, kept their ductility up to 200 Mrad or more, and the rate of increase in elastic modulus as well as yield strength with the increasing irradiation dose was considerably lower than that of untreated or crosslinked polyethylene. The effect of the grafting extent, and that of the irradiation dose-rate on the fracture energy were also examined. The weight increase of polyethylene due to the oxygen consumption and the resulting formation of carbonyl group which proceeded proportionally with the irradiation dose were remarkably suppressed by the grafting, whereas the double bond formation seemed to be unaffected by it. The grafted film held the original content of gel fraction unchanged during the irradiation in air, but the average molecular weight of the sol fraction decreased gradually. Meanwhile, the gel fraction of the crosslinked polyethylene was degenerated by a small dose of irradiation. The analysis of gaseous products revealed the formation of water, methanol, acetaldehyde and so forth from the irradiated grafted film. The grafting procedure and the subsequent irradiation of the grafted film did not affect the degree of crystallinity of the backbone polyethylene. The role played by the grafted polyacenaphthylene for endowing the radiation resistivity to polyethylene and its inherent limitation in effect were discussed from the structural point of view of the grafted film.

  14. Which polyesters can mimic polyethylene?

    PubMed

    Stempfle, Florian; Ortmann, Patrick; Mecking, Stefan

    2013-01-11

    Self-metathesis of erucic acid by [(PCy(3))(η-C-C(3)H(4)N(2)Mes(2))Cl(2)Ru = CHPh] (Grubbs second- generation catalyst) followed by catalytic hydrogenation and purification via the ester yields 1,26-hexacosanedioate (>99% purity). Polyesterification with 1,26-hexacosanediol, generated from the diester, affords polyester-26,26, which features a T(m) of 114 °C (T(c) = 92 °C, ΔH(m) = 160 J g(-1)). Ultralong-chain model polyesters-38,23 (T(m) = 109 °C) and -44,23 (T(m) = 111 °C), generated via multistep procedures including acyclic diene metathesis polymerization, underline that melting points of such aliphatic polyesters do not gradually increase with methylene sequence chain length. Available data suggest that to mimic linear polyethylenes thermal properties, even longer sequences, amounting to at least four times a fatty acid chain, fully incorporated in a linear fashion are required.

  15. 40 CFR 721.1729 - Boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... polyethylene glycol mono-Bu ether and polyethylene glycol mono Me ether. 721.1729 Section 721.1729 Protection... acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol mono Me ether... identified as boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene...

  16. 40 CFR 721.1729 - Boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... polyethylene glycol mono-Bu ether and polyethylene glycol mono Me ether. 721.1729 Section 721.1729 Protection... acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol mono Me ether... identified as boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene...

  17. 40 CFR 721.1729 - Boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... polyethylene glycol mono-Bu ether and polyethylene glycol mono Me ether. 721.1729 Section 721.1729 Protection... acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol mono Me ether... identified as boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene...

  18. 40 CFR 721.1729 - Boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... polyethylene glycol mono-Bu ether and polyethylene glycol mono Me ether. 721.1729 Section 721.1729 Protection... acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol mono Me ether... identified as boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene...

  19. 40 CFR 721.1729 - Boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... polyethylene glycol mono-Bu ether and polyethylene glycol mono Me ether. 721.1729 Section 721.1729 Protection... acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene glycol mono Me ether... identified as boric acid (H3BO3), mixed esters with polyethylene glycol mono-Bu ether and polyethylene...

  20. 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.

  1. Incorporation of isosorbide into poly(butylene terephthalate) via solid-state polymerization.

    PubMed

    Sablong, Rafaël; Duchateau, Robbert; Koning, Cor E; de Wit, Gert; va Es, Daan; Koelewijn, Roelof; van Haveren, Jacco

    2008-11-01

    The biomass-based monomer isosorbide was incorporated into poly(butylene terephthalate) (PBT) by solid-state polymerization (SSP) using the macrodiol monomer BTITB-(OH) 2, which consists of isosorbide (I), terephthalic acid (T), and 1,4-butandiol (B) residues. This macromonomer can be synthesized by a simple one-pot, two-step reaction. Polymers with number-average molecular weights up to 100,000 g x mol (-1) were readily synthesized from various ratios of PBT/BTITB-(OH) 2. Their molecular weights, thermal properties, and colors were compared with corresponding copolyesters that were obtained by melt polycondensation. We found that T m, T c, and especially T g were superior for materials that were obtained by SSP. This is ascribed to differences in the microstructures of both types of copolyesters; the SSP products exhibit a more blocky structure than do the more random melt-polymerized counterparts. The SSP method resulted in much higher molecular weights and much less colored polymers, and it seems to be the preferred route for incorporating biobased monomers that exhibit limited thermal stability into engineering plastics.

  2. Biodegradability enhancement of purified terephthalic acid wastewater by coagulation-flocculation process as pretreatment.

    PubMed

    Karthik, Manikavasagam; Dafale, Nishant; Pathe, Pradyumna; Nandy, Tapas

    2008-06-15

    In this work, the coagulation-flocculation process was used as pretreatment for purified terephthalic acid (PTA) wastewater with the objective of improving its overall biodegradability. PTA production generates wastewaters with toxicants p-xylene [1,4-dimethyl-benzene (C8H10)], a major raw material used in the production process, along with some of the intermediates, viz., p-toluic acid, benzoic acid, 4-carboxybenzaldehyde, phthalic acid and terephthalic acid. These compounds affect the bio-oxidation process of wastewater treatment; hence removal of these constituents is necessary, prior to conventional aerobic treatment. This paper addresses the application of coagulation-flocculation process using chemical coagulants, viz., aluminium sulphate (alum), polyaluminium chloride (PAC), ferrous sulphate and ferric chloride in combination with anionic polyelectrolyte. Polyaluminium chloride (PAC) in conjunction with lime and polyelectrolyte removed about 63.1% chemical oxygen demand (COD) and 45.2% biochemical oxygen demand (BOD) from PTA wastewater. Coagulation-flocculation process coupled with aerobic bio-oxidation treatment of PTA wastewater achieved, COD & BOD removals of 97.4% and 99.4%, respectively. The biodegradability enhancement evaluated in terms of the BOD5/COD ratio, increased from 0.45 to 0.67 at the optimum conditions. The results obtained from these studies indicate that the coagulation-flocculation process could be a suitable pretreatment method in reducing toxicity of PTA wastewater whilst enhancing biodegradability for aerobic biological treatment scheme.

  3. 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

  4. 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.

  5. Polyethylene Glycol Camouflaged Earthworm Hemoglobin

    PubMed Central

    Moges, Selamawit; Nacharaju, Parimala; Roche, Camille; Dantsker, David; Palmer, Andre; Friedman, Joel M.

    2017-01-01

    Nearly 21 million components of blood and whole blood and transfused annually in the United States, while on average only 13.6 million units of blood are donated. As the demand for Red Blood Cells (RBCs) continues to increase due to the aging population, this deficit will be more significant. Despite decades of research to develop hemoglobin (Hb) based oxygen (O2) carriers (HBOCs) as RBC substitutes, there are no products approved for clinical use. Lumbricus terrestris erythrocruorin (LtEc) is the large acellular O2 carrying protein complex found in the earthworm Lumbricus terrestris. LtEc is an extremely stable protein complex, resistant to autoxidation, and capable of transporting O2 to tissue when transfused into mammals. These characteristics render LtEc a promising candidate for the development of the next generation HBOCs. LtEc has a short half-life in circulation, limiting its application as a bridge over days, until blood became available. Conjugation with polyethylene glycol (PEG-LtEc) can extend LtEc circulation time. This study explores PEG-LtEc pharmacokinetics and pharmacodynamics. To study PEG-LtEc pharmacokinetics, hamsters instrumented with the dorsal window chamber were subjected to a 40% exchange transfusion with 10 g/dL PEG-LtEc or LtEc and followed for 48 hours. To study the vascular response of PEG-LtEc, hamsters instrumented with the dorsal window chamber received multiple infusions of 10 g/dL PEG-LtEc or LtEc solution to increase plasma LtEc concentration to 0.5, then 1.0, and 1.5 g/dL, while monitoring the animals’ systemic and microcirculatory parameters. Results confirm that PEGylation of LtEc increases its circulation time, extending the half-life to 70 hours, 4 times longer than that of unPEGylated LtEc. However, PEGylation increased the rate of LtEc oxidation in vivo. Vascular analysis verified that PEG-LtEc showed the absence of microvascular vasoconstriction or systemic hypertension. The molecular size of PEG-LtEc did not change the

  6. 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.

  7. 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...

  8. Ear reconstruction with porous polyethylene implants.

    PubMed

    Berghaus, Alexander; Stelter, Klaus; Naumann, Andreas; Hempel, John Martin

    2010-01-01

    This article describes a surgical technique using porous polyethylene as the framework material for ear reconstruction. In comparison to the use of rib cartilage, porous polyethylene - first described by Berghaus in 1982 - provides better definition and projection as well as congruency with the opposite side. Hospitalization time is significantly shorter. There are less surgical interventions than with traditional microtia operations that use rib cartilage, and the patient is spared the additional procedure needed to remove the rib cartilage, with all the associated complications as well as the resulting thorax scar. Also, reconstruction can take place at an earlier age, which is advantageous for those concerned. Using porous polyethylene as the frame material, a temporoparietal flap and full-thickness skin cover, we have been able to achieve very convincing results over recent years.

  9. 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.

  10. Contact urticaria due to polyethylene gloves.

    PubMed

    Sugiura, Keiji; Sugiura, Mariko; Shiraki, Rika; Hayakawa, Ritsuko; Shamoto, Mikihiro; Sasaki, Kazumi; Itoh, Akira

    2002-05-01

    We report a rare case of contact urticaria due to polyethylene gloves. The patient, a 46-year-old cook, had had had chronic urticaria since 1985, and first visited our hospital in June 2000. We began by prescribing antihistamine and antiallergenic drugs for him, but his condition did not improve. From a detailed interview, we established that when he put on polyethylene gloves at work, his condition worsened. We suspected some component of his gloves to be the cause of his symptoms. Prick and scratch tests with a solution extracted from his gloves showed a wheal-and-flare reaction at 15 min. We advised him to wear a cotton shirt under his clothes in daily life, and to put on cotton gloves under his polyethylene gloves while at work. Subsequently, the size and the number of wheals were markedly smaller and the subject's symptoms were reduced.

  11. Nasal reconstruction using porous polyethylene implants.

    PubMed

    Romo, T; Sclafani, A P; Jacono, A A

    2000-01-01

    Nasal reconstruction presents a significant challenge to the facial plastic surgeon. The dual goals of reconstruction are restoration of the desired aesthetic nasal contour and an improved nasal airway. Autologous cartilage and bone are considered optimal grafting material, but their supply is often limited and harvesting entails additional morbidity. Many synthetic materials have been introduced in nasal reconstruction, but high infection and extrusion rates limited their use. Porous high density polyethylene implants present an alternative to autologous material as they allow for fibrovascular ingrowth, leading to stability of the implant and decreased rates of infection. Herein we describe the use of porous high density polyethylene implants for reconstruction of the platyrrhine nose and in revision rhinoplasty. The use of preformed nasal-dorsal tip and alar batten implants are described, as well as the use of columellar strut and premaxillary plumper implants. We believe that porous high density polyethylene implants provide a safe, desirable alternative in functional and aesthetic nasal reconstruction.

  12. Radiative Cooling With Pigmented Polyethylene Foils

    NASA Astrophysics Data System (ADS)

    Niklasson, Gunnar A.; Eriksson, Tord S.

    1989-03-01

    Polyethylene foils containing a nonabsorbing pigment can be suitable for radiative cooling because of their high reflectance of solar radiation combined with a high transmittance in the atmospheric window region in the thermal infrared. We have studied the optical properties in the wavelength range 0.3-50 μm of extruded polyethylene foils containing various amounts of 0.23 μm diameter Ti02 particles. It appears that the foils can prevent heating of an underlying material, even when directly illuminated by the sun. The total transmittance and reflectance of the Ti02-polyethylene foils were compared with multiple scattering calculations. Lorenz-Mie theory was used to model the scattering and absorption of a single TiO2 sphere. The single scattering parameters were then introduced into the four flux theory, by which the transmittance and reflectance were calculated. We find a satisfactory agreement between theory and experiments in most cases.

  13. 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...

  14. NOVEL BINDER SYSTEMS DERIVED FROM POLY(ETHYLENE TEREPHTHALATE) PET WASTE FOR SOLVENTLESS MAGNETIC TAPE MANUFACTURING: INVESTIGATION OF THE MECHANICAL PROPERTIES OF THE ACRYLATED OLIGOMERS. (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...

  15. 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...

  16. NOVEL BINDER SYSTEMS DERIVED FROM POLY(ETHYLENE TEREPHTHALATE) PET WASTE FOR SOLVENTLESS MAGNETIC TAPE MANUFACTURING: INVESTIGATION ON THE MECHANICAL PROPERTIES OF THE 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...

  17. 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...

  18. 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...

  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. SiOx layer as functional barrier in polyethylene terephthalate (PET) bottles against potential contaminants from post-consumer recycled PET.

    PubMed

    Welle, Frank; Franz, Roland

    2008-06-01

    The barrier effect of a silicon oxide (SiOx) coating on the inner surface of PET bottles, in terms of the ability to reduce the migration of post-consumer compounds from the PET bottle wall into food simulants (3% acetic acid and 10% ethanol), was investigated. The barrier effect was examined by artificially introducing model substances (surrogates) into the PET bottle wall to represent a worst-case scenario. Test bottles with three different spiking levels up to approximately 1000 mg kg(-1) per surrogate were blown and coated on the inner surface. The SiOx-coated bottles and the non-coated reference bottles were filled with food simulants. From the specific migration of the surrogates with different bottles wall concentrations, the maximum surrogate concentrations in the bottle wall corresponding to migration of 10 microg l(-1) were determined. It was shown that the SiOx coating layer is an efficient barrier to post-consumer compounds. The maximum bottle wall concentrations of the surrogates corresponding to migration of 10 microg l(-1) were in the range of 200 mg kg(-1) for toluene and approximately 900 mg kg(-1) for benzophenone. Consequently, the SiOx coating allows use of conventionally recycled post-consumer PET flakes (without a super-clean recycling process) for packaging aqueous and low alcoholic foodstuffs (under cold-fill conditions) and protects food from migration of unwanted contaminants from post-consumer PET.

  1. 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.

  2. The Effects of Sugars on the Biofilm Formation of Escherichia coli 185p on Stainless Steel and Polyethylene Terephthalate Surfaces in a Laboratory Model

    PubMed Central

    Khangholi, Mahdi; Jamalli, Ailar

    2016-01-01

    Background Bacteria utilize various methods in order to live in protection from adverse environmental conditions. One such method involves biofilm formation; however, this formation is dependent on many factors. The type and concentration of substances such as sugars that are present in an environment can be effective facilitators of biofilm formation. Methods First, the physico-chemical properties of the bacteria and the target surface were studied via the MATS and contact angle measurement methods. Additionally, adhesion to different surfaces in the presence of various concentrations of sugars was compared in order to evaluate the effect of these factors on the biofilm formation of Escherichia coli, which represents a major food contaminant. Results Results showed that the presence of sugars has no effect on the bacterial growth rate; all three concentrations of sugars were hydrophilic and demonstrated a high affinity toward binding to the surfaces. Conclusions The impact of sugars and other factors on biofilm formation can vary depending on the type of bacteria present. PMID:27800149

  3. Atmospheric cold plasma inactivation of Escherichia coli 0157:H7 and aerobic microorganisms in cold-stored romaine lettuce packaged in a commerical polyethylene terephthalate container

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Leafy greens continue to be a significant vector for foodborne pathogens, including Escherichia coli O157:H7. Dielectric barrier discharge atmospheric cold plasma (ACP) treatment is a promising method for microbial decontamination of produce. An important aspect of this technology is the potential f...

  4. Inactivation of Escherichia coli 0157:H7 and aerobic microorganisms in Romaine lettuce packaged in a commercial polyethylene terephthalate container using atmospheric cold plasma

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The effects of dielectric barrier discharge atmospheric cold plasma (DACP) treatment on the inactivation of Escherichia coli O157:H7 and aerobic microorganisms in Romaine lettuce packaged in a conventional commercial plastic container were evaluated during storage at 4 degrees C for 7 days. Effects ...

  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 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...

  7. 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...

  8. 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...

  9. 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...

  10. 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...

  11. 21 CFR 178.3760 - Polyethylene glycol (400) monolaurate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true 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...

  12. 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)...

  13. 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...

  14. 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...

  15. 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...

  16. 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...

  17. 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...

  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 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...

  20. 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...

  1. 21 CFR 177.1630 - Polyethylene phthalate polymers.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene phthalate polymers. 177.1630 Section... (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1630 Polyethylene phthalate polymers. Polyethylene phthalate...

  2. Evaluation of Paulownia elongata wood polyethylene composites

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Paulownia wood flour (PWF), a byproduct of milling lumber, was employed as a bio-filler and blended with high density polyethylene (HDPE) via extrusion. Paulownia wood (PW) shavings were milled through a 1-mm screen then separated via shaking into various particle fractions using sieves (#30 - < #2...

  3. 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.

  4. 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)

  5. 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...

  6. High-pressure vibrational properties of polyethylene

    NASA Astrophysics Data System (ADS)

    Fontana, Luca; Santoro, Mario; Bini, Roberto; Vinh, Diep Q.; Scandolo, Sandro

    2010-11-01

    The pressure evolution of the vibrational spectrum of polyethylene was investigated up to 50 GPa along different isotherms by Fourier-transform infrared and Raman spectroscopy and at 0 K by density-functional theory calculations. The infrared data allow for the detection of the orthorhombic Pnam to monoclinic P21/m phase transition which is characterized by a strong hysteresis both on compression and decompression experiments. However, an upper and lower boundary for the transition pressure are identified. An even more pronounced hysteresis is observed for the higher-pressure transition to the monoclinic A2/m phase. The hysteresis does not allow in this case the determination of a well defined P-T transition line. The ambient structural properties of polyethylene are fully recovered after compression/decompression cycles indicating that the polymer is structurally and chemically stable up to 50 GPa. A phase diagram of polyethylene up to 50 GPa and 650 K is proposed. Analysis of the pressure evolution of the Davydov splittings and of the anomalous intensification with pressure of the IR active wagging mode provides insight about the nature of the intermolecular interactions in crystalline polyethylene.

  7. 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.

  8. Treatment of the terephthalic acid-containing wastewater using a biological-aerated filter.

    PubMed

    Zhang, Wen-Yi; Zhang, Cai-Qin; Liu, Liang; Shen, Rong-Yan; Han, Xiao-Jing

    2014-01-01

    In this paper, the biological-aerated filter (BAF) was employed to treat the wastewater containing terephthalic acid (TA). Factors that affected the efficiency of TA and CODCr removal were evaluated experimetally, including pH, hydraulic loading, hydraulic retention time (HRT) and TA volume loading. At pH 7-8, hydraulic loading rate 0.067-0.48 m3/(m2 h), HRT more than 3.5h and TA loading 0.04-0.15g/(m3 d), the TA and CODCr removal efficiency was more than 93% and 87%, respectively. The mathematical model of matrix (TA) was obtained by Monod's relation and the experimental parameters of the model were 1.972 g/(m2d) and 9.782 mg/L.

  9. 4-[(E)-2-(Pyridin-2-yl)ethen-yl]pyridine-terephthalic acid (2/1).

    PubMed

    Castro-Montes, Paola; Guerrero-Alvarez, Jorge A; Hopfl, Herbert; Campos-Gaxiola, Jose J; Cruz-Enriquez, Adriana

    2012-12-01

    The title 2:1 co-crystal, 2C12H10N2·C8H6O4, crystallizes with one mol-ecule of 4-[(E)-2-(pyridin-2-yl)ethen-yl]pyridine (A) and one half-mol-ecule of terephthalic acid (B) in the asymmetric unit. In the crystal, the components are linked through heterodimeric COOH⋯Npyridine synthons, forming linear aggregates of composition -A-B-A-B-. Further linkage through weak C-H⋯O and C-H⋯π inter-actions gives two-dimensional hydrogen-bonded undulating sheets propagating in the [100] and [010] directions. These layers are connected through additional weak C-H⋯O contacts, forming a three-dimensional structure.

  10. [Analysis on the components of rat urinary stone induced by terephthalic acid].

    PubMed

    Qi, Shaoting; Wang, Xinru; Xu, Xikun; Yao, Hongwei

    2002-04-01

    In order to analyze the components of rat urinary stone and to explore the possible mechanism of chemically induced bladder cancer, terephthalic acid (TPA) is orally administrated to rats at the doses of 5000 and 500 mg/kg/BW/everyday for consecutive 90 days and stones in bladder and kidney are collected. Inductive Coupled Plasma Quantomer (ICP), Element Analyzer (EA) and Fourier Transform Infared Spectrometer (FT-IR) are applied for the analysis on the components of stone in bladder and kidney. The results showed that the main components of the stone are calcium, carbon, nitrogen, hydrogen and phosphorus. The FT-IR showed that the stones both in bladder and kidney might contain nitrous, carbonate, ammonium salt, and para-position replaced benzene-ring compounds, but no original TPA is detected. The findings indicate that TPA might have a metabolic turnover inside the rat body, and, at least, might not be completely excreted in its original form.

  11. Bis(2-amino-4-methyl­pyridinium) terephthalate tetra­hydrate

    PubMed Central

    Hemamalini, Madhukar; Fun, Hoong-Kun

    2010-01-01

    In the crystal structure of the title salt, 2C6H9N2 +·C8H4O4 2−·4H2O, the terephthalate carboxyl­ate groups inter­acts with the 2-amino-4-methyl­pyridinium cations via a pair of N—H⋯O hydrogen bonds, forming an R 2 2(8) ring motif. The water mol­ecules form an R 6 6(12) ring motif through O—H⋯O hydrogen bonds and these motifs are fused, forming a supra­molecular chain along the c axis. The R 2 2(8) and R 6 6(12) ring motifs are connected via O—H⋯O hydrogen bonds. In addition, π–π stacking inter­actions are observed between the pyridinium rings [centroid–centroid distance = 3.522 (12) Å]. PMID:21588255

  12. 1,4-Bis(imidazol-1-yl)benzene–terephthalic acid (1/1)

    PubMed Central

    Zhang, Shiyong; Tang, Yurong; Mao, Zhihua; Li, Mingliang; Lan, Jingbo; Su, Xiaoyu

    2009-01-01

    In the title compound, C12H10N4·C8H6O4, 1,4-bis­(imidazol-1-yl)benzene and terephthalic acid mol­ecules are joined via strong O—H⋯N hydrogen bonds to form infinite zigzag chains. Both mol­ecules are located on crystallographic inversion centers. The O—H⋯N hydrogen-bonded chains are assembled into two-dimensional layers through weak C—H⋯O and strong π–π stacking inter­actions [centroid–centroid distance = 3.818 (2) Å], leading to the formation of a three-dimensional supra­molecular structure. PMID:21581669

  13. 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.

  14. Analytical rheology of metallocene-catalyzed polyethylenes

    NASA Astrophysics Data System (ADS)

    Shanbhag, Sachin; Takeh, Arsia

    2011-03-01

    A computational algorithm that seeks to invert the linear viscoelastic spectrum of single-site metallocene-catalyzed polyethylenes is presented. The algorithm uses a general linear rheological model of branched polymers as its underlying engine, and is based on a Bayesian formulation that transforms the inverse problem into a sampling problem. Given experimental rheological data on unknown single-site metallocene- catalyzed polyethylenes, it is able to quantitatively describe the range of values of weight-averaged molecular molecular weight, MW , and average branching density, bm , consistent with the data. The algorithm uses a Markov-chain Monte Carlo method to simulate the sampling problem. If, and when information about the molecular weight is available through supplementary experiments, such as chromatography or light scattering, it can easily be incorporated into the algorithm, as demonstrated. Financial support from NSF DMR 0953002.

  15. 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.)

  16. Comparative wear tests of ultra-high molecular weight polyethylene and cross-linked polyethylene.

    PubMed

    Harsha, A P; Joyce, Tom J

    2013-05-01

    Wear particle-induced osteolysis is a major concern in hip implant failure. Therefore, recent research work has focussed on wear-resistant materials, one of the most important of which is cross-linked polyethylene. In view of this, the objective of this study was to compare the in vitro wear performance of cross-linked polyethylene to traditional ultra-high molecular weight polyethylene. In order to mimic appropriate in vivo conditions, a novel high-capacity wear tester called a circularly translating pin-on-disc was used. The results of this in vitro study demonstrated that the wear rate for cross-linked polyethylene was about 80% lower than that of conventional ultra-high molecular weight polyethylene. This difference closely matches in vivo results reported in the literature for total hip replacements that use the two biopolymers. The in vitro results were also verified against ASTM F732-00 (standard test method for wear testing of polymeric materials for use in total joint prostheses). The 50-station circularly translating pin-on-disc proved to be a reliable device for in vitro wear studies of orthopaedic biopolymers.

  17. 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.

  18. 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.

  19. Degradability of dimethyl terephthalate by Variovorax paradoxus T4 and Sphingomonas yanoikuyae DOS01 isolated from deep-ocean sediments.

    PubMed

    Wang, Yu Ping; Gu, Ji-Dong

    2006-08-01

    Two strains of bacteria were isolated from deep-ocean sediments of the South China Sea using enrichment culturing technique and they were identified as Sphingomonas yanoikuyae DOS01 (AY878409) and Variovorax paradoxus T4 (AY878410) based on 16S rRNA gene sequences. S. yanoikuyae DOS01 was only capable of transforming dimethyl terephthalate (DMTP) to monomethyl terephthalate (MMTP) without further degradation while V. paradoxus T4 exhibited ability in mineralizing DMTP as the sole source of carbon and energy. The biochemical pathway of DMTP degradation was through MMTP and terephthalic acid (TA) as major detectable degradation intermediates in the culture media by both microorganisms. V. paradoxus T4 utilized DMTP and MMTP via hydrolysis of diester and monoester in the initial steps in degradation as confirmed by total organic carbon analysis of the culture medium and esterase activity assay of the lysed cells and fraction. The specific hydrolysis activity of esterase induced by DMTP or MMTP showed that greater hydrolysis of p-nitrophenyl acetate by esterase induced by DMTP-grown cells than that induced by MMTP. Results of this research suggest that the cleavage of the two identical carboxylic ester groups of phthalate diester are carried out by highly specific esterases of the same bacteria in the environment.

  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. Preparation of extruded polyethylene/chitosan blends compatibilized with polyethylene-graft-maleic anhydride.

    PubMed

    Quiroz-Castillo, J M; Rodríguez-Félix, D E; Grijalva-Monteverde, H; Del Castillo-Castro, T; Plascencia-Jatomea, M; Rodríguez-Félix, F; Herrera-Franco, P J

    2014-01-30

    Novel films of polyethylene and chitosan were obtained using extrusion. These polymers have interesting properties, and processing them with methods that are of high use in the industry, such as the extrusion method, can have a significant effect on the potential applications of these materials. The individual materials were thermally characterized; after this, extruded films of low density polyethylene and chitosan mixtures were prepared with the addition of polyethylene-graft-maleic anhydride as a compatibilizer for the blends, and glycerol, as a plasticizer for chitosan. The use of compatibilizer and plasticizer agents improved the processability and compatibility of the mixtures, as well as their mechanical properties, as revealed by mechanical property measurements and scanning electron microscopy. It was possible to prepare blends with a maximum chitosan content of 20 wt%. The material stiffness increased with the increase of chitosan in the sample. FTIR studies revealed the existence of an interaction between the compatibilizer and chitosan.

  2. Patient sensitivity to polyethylene particles with cemented total hip arthroplasty.

    PubMed

    Ise, Kentaro; Kawanabe, Keiichi; Matsusaki, Takashi; Shimizu, Motoyuki; Onishi, Eijiro; Nakamura, Takashi

    2007-10-01

    To determine whether sensitivity to polyethylene particles varies among patients, we studied 25 patients who had undergone total hip arthroplasty. We used pelvic radiographs to measure annual polyethylene wear and the area of osteolysis. The ratio of the area of osteolysis to the volumetric polyethylene wear was defined as sensitivity index. Adherent cells from peripheral blood were cocultured with polyethylene particles, and the amount of bone-resorptive cytokines was measured. The amount of interleukin-6, but not of interleukin-1beta or tumor necrosis factor-alpha, released from adherent cells in the in vitro experiment correlated with the in vivo sensitivity indices. This technique appears capable of predicting the development of polyethylene-induced osteolysis, allowing surgeons to avoid using polyethylene as the bearing surface in patients at risk for osteolysis.

  3. Lewis acid/base character and crystallisation properties of poly(butylene terephthalate).

    PubMed

    Santos, José M R C A; Guthrie, James T

    2015-01-30

    Two grades of poly(butylene terephthalate) were analysed by means of inverse gas chromatography (IGC) and the results correlated with the respective crystallisation properties. The following parameters were determined by IGC: the dispersive component of the surface tension, the enthalpy and the entropy of adsorption of selected polar and apolar probes, and the Lewis acidity and basicity constants, Ka and Kb respectively. The interpretation of the values determined for Ka and Kb is in agreement with the FTIR spectra relating to the carboxyl end-group and the hydroxyl end-group concentrations in these polymers. The differences in the molecular weight values and in the end-group type and concentration, between the two grades of PBT, do not cause differences in the crystallisation activation energy. This observation suggests that there is a leading contribution of the Lewis basic sites to the crystallisation activation energy of the grades of PBT that were analysed. However, the lower value of Ka and the greater molar mass of one of the PBT grades lead to a corresponding lower crystallisation degree.

  4. A new brominated polymeric additive for flame retardant glass-filled polybutylene terephthalate

    NASA Technical Reports Server (NTRS)

    Nir, Z.; Kourtides, D. A.; Parker, J. A.; Bar-Yaacov, Y.; Minke, R.; Touval, I.

    1982-01-01

    Attention is called to the undesirable effects (poor ultraviolet light stability and blooming) sometimes introduced by brominated flame retarders. A brominated polymeric additive (BPA) with little or none of these undesirable side effects is compared with decabromobiphenyl oxide (DBBPO). The additive bears the product name F-2300. It is found to be more easily dispersed than DBBPO. The F-2300 is as effective as the DBBPO in the oxygen index test. The improved efficiency of the F-2300 may be explained by its better dispersion in polybutylene terephthalate (PBT). Glass-filled PBT containing F-2300 is found to be more resistant to UV degradation than DBBPO-containing formulas. Formulations with F-2300 therefore have a longer useful outdoor life. F-2300 is a diglycidyl-type polymer containing 50 percent aromatically bound bromine. Its melting point is 112 C, and it is stable up to 372 C. It is pointed out that since its melts at a relatively low temperature, it can be introduced into the formulation as a large agglomerate and still be dispersed evenly throughout the polymer.

  5. Toxicity of purified terephthalic acid manufacturing wastewater on reproductive system of male mice (Mus musculus).

    PubMed

    Zhang, Xu-Xiang; Sun, Shi-Lei; Zhang, Yan; Wu, Bing; Zhang, Zong-Yao; Liu, Bo; Yang, Liu-Yan; Cheng, Shu-Pei

    2010-04-15

    Reproductive toxicity of purified terephthalic acid (PTA) manufacturing wastewater on the male mice (Mus musculus) was investigated after 35-day intragastric perfusion treatment with the wastewater. Fluorescein diacetate and propidium iodide staining, and flow cytometry were used to assess the toxicity of PTA wastewater on spermatogenic cells. PTA wastewater induced significant variations in the relative percentages of immature haploid, diploid, tetraploid and S-phase spermatogonia. Percentage of viable spermatogenic cells was reduced from 93.1+/-2.3 in control group to 90.4+/-1.9 in the wastewater-treated group. Testicular histopathology revealed expansion of interstitial space and reduction in the number and size of Leydig cells induced by the wastewater, which was further certified by the decrease (10.6%) in relative testes weight and the increase (101.3%) in sperm shape abnormality in the wastewater-treated group. In this study, PTA wastewater was found to have reproductive toxicity on male mice, and public health problems may potentially arise from the discharge of the wastewater into the environment.

  6. [Electricity generation using high concentration terephthalic acid solution by microbial fuel cell].

    PubMed

    Ye, Ye-Jie; Song, Tian-Shun; Xu, Yuan; Chen, Ying-Wen; Zhu, She-Min; Shen, Shu-Bao

    2009-04-15

    The high concentration terephthalic acid (TA) solution as the substrate of microbial fuel cell (MFC) was studied to generate electricity. The open circuit voltage was 0.54 V after inoculating for 210 h with anaerobic activated sludge, which proved that TA can be the substrate of microbial fuel cell to generate electricity. The influence of pH and substrate concentration on generating electricity was studied deeply. The voltage output of external resistance (R = 1,000 Omega) was the highest when pH was 8.0. It increased as the substrate concentration increasing and tended towards a maximum value. The maximum voltage output Umax was 0.5 V and Ks was 785.2 mg/L by Monod equation regression. When the substrate concentration (according to COD) was 4000 mg/L, the maximum power density was 96.3 mW/m2, coulomb efficiency was 2.66% and COD removal rate was 80.3%.

  7. Pulse respirometry in two-phase partitioning bioreactors: case study of terephthalic acid biodegradation.

    PubMed

    Ordaz, Alberto; Quijano, Guillermo; Thalasso, Frederic; Garibay-Orijel, Claudio

    2013-02-01

    Two-phase partitioning bioreactors (TPPBs) are based on the addition of an organic phase, often called vector, to a bioreactor in order to increase mass transfer of oxygen or gaseous substrates from the gaseous phase to the aqueous phase. In TPPBs, like in any other reactor design, the characterization of the bioprocess is often required for design, control, and operation purposes. Pulse respirometry is a method that allows for microbial processes characterization through the determination of several stoichiometric and kinetic parameters with relatively little experimental effort. Despite its interest and its previous application in countless applications, pulse respirometry has never been applied in TPPBs. In this work, pulse respirometry was assessed in a model TPPB degrading terephthalic acid and using Elvax™ as solid vector to enhance oxygen transfer. The results indicated that the addition of 10 to 20% Elvax increased oxygen transfer by up to 97%, compared to control with no vector. Pulse respirometry was successfully applied and allowed for the determination of the growth yield, the substrate affinity constant, and the maximum growth rate, within other. It is concluded that pulse respirometry is a useful method, not only for the characterization of processes in TPPBs but also for the selection of a vector within several brands commercially available.

  8. Characterization of a poly(butylene adipate-co-terephthalate)- hydrolyzing lipase from Pelosinus fermentans.

    PubMed

    Biundo, Antonino; Hromic, Altijana; Pavkov-Keller, Tea; Gruber, Karl; Quartinello, Felice; Haernvall, Karolina; Perz, Veronika; Arrell, Miriam S; Zinn, Manfred; Ribitsch, Doris; Guebitz, Georg M

    2016-02-01

    Certain α/β hydrolases have the ability to hydrolyze synthetic polyesters. While their partial hydrolysis has a potential for surface functionalization, complete hydrolysis allows recycling of valuable building blocks. Although knowledge about biodegradation of these materials is important regarding their fate in the environment, it is currently limited to aerobic organisms. A lipase from the anaerobic groundwater organism Pelosinus fermentans DSM 17108(PfL1) was cloned and expressed in Escherichia coli BL21-Gold (DE3) and purified from the cell extract. Biochemical characterization with small substrates showed thermoalkalophilic properties (Topt=50 °C, pHopt=7.5) and higher activity towards para-nitrophenyl octanoate (12.7 U mg(-1)) compared to longer and shorter chain lengths (C14 0.7 U mg(-1) and C2 4.3 U mg(-1), respectively). Crystallization and determination of the 3-D structure displayed the presence of a lid structure and a zinc ion surrounded by an extra domain. These properties classify the enzyme into the I.5 lipase family. PfL1 is able to hydrolyze poly(1,4-butylene adipate-co-terephthalate) (PBAT) polymeric substrates. The hydrolysis of PBAT showed the release of small building blocks as detected by liquid chromatography mass spectrometry (LC-MS). Protein dynamics seem to be involved with lid opening for the hydrolysis of PBAT by PfL1.

  9. 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.

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. Polyethylene glycol as a solid polymer electrolyte

    SciTech Connect

    Cha, D.K.; Park, S.M.

    1997-12-01

    Polymer electrolytes were prepared from polyethylene glycol (PEG)-lithium perchlorate complexes and characterized at a stainless steel electrode using a variety of electrochemical techniques. The charge transfer process was affected by the oxide film on the stainless steel electrode surface in the early stages of redox processes. The polymer electrolytes showed a transference number of 0.2 for Li{sup +}. The conductivity of the PEG-10000 electrolyte has been determined to be 4.7 {times} 10{sup {minus}5} S/cm. This rather high value is attributed to the anionic end groups increasing the polarity of the matrix.

  15. 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.

  16. 78 FR 28192 - Polyethylene Retail Carrier Bags From Thailand: Preliminary Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-05-14

    ... International Trade Administration Polyethylene Retail Carrier Bags From Thailand: Preliminary Results of... administrative review of the antidumping duty order on polyethylene retail carrier bags (PRCBs) from Thailand... antidumping duty order is polyethylene retail carrier bags, which are currently classified under...

  17. 78 FR 76567 - Tall Oil, Polymer With Polyethylene Glycol and Succinic Anhydride Monopolyisobutylene Derivs...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-12-18

    ... AGENCY 40 CFR Part 180 Tall Oil, Polymer With Polyethylene Glycol and Succinic Anhydride... oil, polymer with polyethylene glycol and succinic anhydride monopolyisobutylene derivs. (CAS Reg. No... residues of tall oil, polymer with polyethylene glycol and succinic anhydride monopolyisobutylene...

  18. Self-Healing of Polyethylene Oxide

    NASA Astrophysics Data System (ADS)

    Chipara, Dorina Magdalena; Flores, Maritza; Puente, Nancy; Lozano, Karen

    2011-03-01

    Autonomic self-healing is expected to enhance the lifetime of polymeric materials, resins, and composites subjected to long term mechanical stresses. The self-healing process is initiated by the rupture of some polyurea-formaldehyde microcapsules filled with monomer. The self-healing polymer is actually a compound containing microcapsules filled with monomer and catalyst particles. The monomer released from these broken microcapsules is diffusing within the polymer, reacting with the catalyst and starting a polymerization reaction. This new polymer, growing within the propagating crack, stops the mechanical failure. While the process is pretty slow (timescale of the order of 10 to 100 s), there are many important technological applications that would benefit from the availability of self-healing polymers. We report about the addition of self-healing capabilities to polyethylene oxide by using polyurea formaldehyde microcapsules filled with dicyclopentadiene and first generation Grubbs catalysts. Details regarding the physical and chemical steps used to add self-healing capabilities to polyethylene oxide will be presented. Self-healing efficiency was assessed by fatigues tests.

  19. 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

  20. 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.

  1. Recycling of irradiated high-density polyethylene

    NASA Astrophysics Data System (ADS)

    Navratil, J.; Manas, M.; Mizera, A.; Bednarik, M.; Stanek, M.; Danek, M.

    2015-01-01

    Radiation crosslinking of high-density polyethylene (HDPE) is a well-recognized modification of improving basic material characteristics. This research paper deals with the utilization of electron beam irradiated HDPE (HDPEx) after the end of its lifetime. Powder of recycled HDPEx (irradiation dose 165 kGy) was used as a filler into powder of virgin low-density polyethylene (LDPE) in concentrations ranging from 10% to 60%. The effect of the filler on processability and mechanical behavior of the resulting mixtures was investigated. The results indicate that the processability, as well as mechanical behavior, highly depends on the amount of the filler. Melt flow index dropped from 13.7 to 0.8 g/10 min comparing the lowest and the highest concentration; however, the higher shear rate the lower difference between each concentration. Toughness and hardness, on the other hand, grew with increasing addition of the recycled HDPEx. Elastic modulus increased from 254 to 450 MPa and material hardness increased from 53 to 59 ShD. These results indicate resolving the problem of further recycling of irradiated polymer materials while taking advantage of the improved mechanical properties.

  2. 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.

  3. 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...

  4. 21 CFR 177.1630 - Polyethylene phthalate polymers.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false 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...

  5. 21 CFR 177.1630 - Polyethylene phthalate polymers.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false 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...

  6. 21 CFR 177.1630 - Polyethylene phthalate polymers.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false 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...

  7. Preparation and Electrical Property of Polypyrrole-Polyethylene Composite

    NASA Astrophysics Data System (ADS)

    Yoshino, Katsumi; Yin, Xiao Hong; Morita, Shigenori; Nakanishi, Yutaka; Nakagawa, Shinichi; Yamamoto, Hideo; Watanuki, Toshiro; Isa, Isao

    1993-02-01

    Polypyrrole-polyethylene composites have been prepared by pressing the mixture of polypyrrole coated and non-coated polyethylene spheres. Electrical conductivity is enhanced by more than 16 orders of magnitude and its activation energy decreases remarkably at concentration of polypyrrole coated polyethylene above around 10-20%, which corresponds to effective polypyrrole concentration of 0.1-0.2%. These characteristics can be explained by a percolation model. That is, at this concentration electrodes are bridged by conducting channel of doped polypyrrole. Thermoelectric power increases in proportion to absolute temperature and is independent on concentration of polypyrrole coated polyethylene sphere above 30%, which support the percolation model. The electrical property of this polypyrrole-polyethylene composite is found to be stable up to 160°C. The application of this composite to the semiconducting layer of a cable has been proposed.

  8. Synthesis, Spectroscopic Properties and Antioxidant Activity of Bis-Hydrazones and Schiff's bases Derived from Terephthalic Dihydrazide.

    PubMed

    Jois, H S Vidyashree; Kalluraya, Balakrishna; Vishwanath, T

    2015-05-01

    A series of novel Schiff base containing bis-1,2,4-triazole and bis-hydrazone derived from terephthalic dihydrazide was synthesized. All the newly synthesized compounds were characterized by (1)H, (13)C NMR, mass spectra, FTIR and elemental analysis. UV-vis spectra and fluorescent spectra of the compounds were recorded. The effect of substituent such as electron withdrawing and electron donating groups on the fluorescent spectra was studied. Also, the comparative discussion on fluorescent spectra of Schiff's base and hydrazones has been described. The antioxidant activity of the compounds revealed that compound 5c and 5f are the most potent compounds in this series.

  9. The adhesion of oxygen-plasma treated poly(ethylene) and poly(ethylene terephthlate) films

    SciTech Connect

    Holton, S.L.; Kinloch, A.J.; Watts, J.F.

    1996-12-31

    The effects of low-pressure oxygen-plasma treatment on the surfaces of poly(ethylene) (PE) and poly(ethylene terephthlate) (PET) films and its influence on the adhesion of PE/PET laminates were assessed. The 90{degree} peel test was used to estimate the adhesive fracture energy, G{sub c} for the laminates. XPS, SEM and AFM were used to analyse the treated films and fracture surfaces. Significant improvements in bond strength occurred within very short treatment times (5s at 50W) with the maximum adhesion occurring after 300s. For longer treatment times the bond strengths decrease slightly. G{sub c} values were found to be low when PET was the peel arm. When PE was the peel arm, the G{sub c} values were substantially larger using the current analysis.

  10. Crystallization Studies of Blends of Low Density Polyethylene and High Density Polyethylene

    NASA Astrophysics Data System (ADS)

    Puig, C.; Gomez, S.; Castañeda, R.

    1997-03-01

    The incorporation of low density polyethylene (LDPE) segments within the high density polyethylene (HDPE) lamellae on cooling from the molten state is investigated using differential scanning calorimetry. Rich LDPE blends (>80%) on quenching from the melt exhibited partial cocrystallization. Two endotherms on heating are observed, the LDPE is the main component of the low melting endotherm whereas the HDPE is the main component of the high melting endotherm. A depression in the high melting temperature peak is observed. In addition, on subsequent treatment the crystallization behaviour under controlled conditions of the low melting component in quenched blends is studied and it shows a shift in the crystallization temperature when compared with pure LDPE. After reheating a depression in the low melting temperature with increasing HDPE content in the blend is observed. The effect of cooling conditions used from the melt on the cocrystallization between the two polymers is studied.

  11. Polyethylene glycol-grafted polystyrene particles.

    PubMed

    Meng, Fenghua; Engbers, Gerard H M; Feijen, Jan

    2004-07-01

    Densely pegylated particles that can serve as a model system for artificial cells were prepared by covalently grafting amino polyethylene glycol (PEG, molecular weight 3400 or 5000) onto carboxyl polystyrene particles (PS-COOH) using carbodiimide chemistry. PEG-modified particles (PS-PEG) were characterized by determination of the PEG surface concentration, zeta-potential, size, and morphology. Under optimized grafting conditions, a dense "brush-like" PEG layer was formed. A PEG surface concentration of approximately 60 pmol/cm2, corresponding with an average distance between grafted PEG chains of approximately 17 A can be realized. It was shown that grafting of PEG onto PS-COOH reduced the adsorption of proteins from human plasma (85 vol %) in phosphate-buffered saline up to 90%.

  12. Polyethylene oxide hydration in grafted layers

    NASA Astrophysics Data System (ADS)

    Dormidontova, Elena; Wang, Zilu

    Hydration of water soluble polymers is one of the key-factors defining their conformation and properties, similar to biopolymers. Polyethylene oxide (PEO) is one of the most important biomedical-applications polymers and is known for its reverse temperature solubility due to hydrogen bonding with water. As in many practical applications PEO chains are grafted to surfaces, e.g. of nanoparticles or planar surfaces, it is important to understand PEO hydration in such grafted layers. Using atomistic molecular dynamic simulations we investigate the details of molecular conformation and hydration of PEO end-grafted to gold surfaces. We analyze polymer and water density distribution as a function of distance from the surface for different grafting densities. Based on a detailed analysis of hydrogen bonding between polymer and water in grafted PEO layers, we will discuss the extent of PEO hydration and its implication for polymer conformation, mobility and layer properties. This research is supported by NSF (DMR-1410928).

  13. Impact behavior of hydroxyapatite reinforced polyethylene composites.

    PubMed

    Zhang, Y; Tanner, K E

    2003-01-01

    Hydroxyapatite particulate reinforced high density polyethylene composite (HA-HDPE) has been developed as a bone replacement material. The impact behavior of the composites at 37 degrees C has been investigated using an instrumented falling weight impact testing machine. The fracture surfaces were examined using SEM and the fracture mechanisms are discussed. It was found that the fracture toughness of HA-HDPE composites increased with HDPE molecular weight, but decreased with increasing HA volume fraction. Examination of fracture surfaces revealed weak filler/matrix interfaces which can debond easily to enable crack initiation and propagation. Increasing HA volume fraction increases the interface area, and more cracks can form and develop, thus decreasing the impact resistance of the composites. Another important factor for the impact behavior of the composites is the matrix. At higher molecular weight, HDPE is able to sustain more plastic deformation and dissipates more impact energy, hence improving the impact property.

  14. Li + grafting of ion irradiated polyethylene

    NASA Astrophysics Data System (ADS)

    Švorčík, V.; Rybka, V.; Vacík, J.; Hnatowicz, V.; Öchsner, R.; Ryssel, H.

    1999-02-01

    Foils of oriented polyethylene (PE) were irradiated with 63 keV Ar + and 155 keV Xe + ions to different fluences at room temperature and then doped from water solution of LiCl. The as irradiated and irradiated plus doped samples were examined by IR, EPR and neutron depth profiling (NDP) technique. The sheet resistance was also measured by the standard two points method. After Li salt doping of ion modified layer of PE, a reaction between degraded macromolecules and Li occur and thus a new chemical structure C-Li + is formed. Owing to the presence of these cations on the polymer chain, the irradiated plus doped layer exhibits higher electric conductivity compared to as-irradiated ones.

  15. Simulation of melting in crystalline polyethylene

    NASA Astrophysics Data System (ADS)

    Zubova, E. A.; Balabaev, N. K.; Musienko, A. I.; Gusarova, E. B.; Mazo, M. A.; Manevitch, L. I.; Berlin, A. A.

    2012-06-01

    We carry out a molecular dynamics simulation of the first stages of constrained melting in crystalline polyethylene (PE). When heated, the crystal undergoes two structural phase transitions: from the orthorhombic (O) phase to the monoclinic (M) phase, and then to the columnar (C), quasi-hexagonal, phase. The M phase represents the tendency to the parallel packing of planes of PE zigzags, and the C phase proves to be some kind of oriented melt. We follow both the transitions O→M and M→C in real time and establish that, at their beginning, the crystal tries (and fails) to pass into the partially ordered phases similar to the RI and RII phases of linear alkanes, correspondingly. We discuss the molecular mechanisms and driving forces of the observed transitions, as well as the reasons why the M and C phases in PE crystals substitute for the rotator phases in linear alkanes.

  16. Vacuum Outgassing of High Density Polyethylene

    SciTech Connect

    Dinh, L N; Sze, J; Schildbach, M A; Chinn, S C; Maxwell, R S; Raboin, P; McLean II, W

    2008-08-11

    A combination of thermogravimetric analysis (TGA) and temperature programmed decomposition (TPD) was employed to identify the outgassing species, the total amount of outgassing, and the outgassing kinetics of high density polyethylene (HDPE) in a vacuum environment. The isoconversional kinetic analysis was then used to analyze the outgassing kinetics and to predict the long-term outgassing of HDPE in vacuum applications at ambient temperature. H{sub 2}O and C{sub n}H{sub x} with n as high as 9 and x centering around 2n are the major outgassing species from solid HDPE, but the quantities evolved can be significantly reduced by vacuum baking at 368 K for a few hours prior to device assembly.

  17. Thermal analysis of polyethylene + X% carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Lozovyi, Fedir; Ivanenko, Kateryna; Nedilko, Sergii; Revo, Sergiy; Hamamda, Smail

    2016-02-01

    The aim of this research is to study the influence of the multi-walled carbon nanotubes (MWCNTs) on the thermomechanical and structural properties of high-density polyethylene. Several, complementary experimental techniques were used, namely, dilatometry, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), Raman spectroscopy, and infrared (IR) spectroscopy. Dilatometry data showed that nanocomposites exhibit anisotropic behavior, and intensity of the anisotropy depends on the MWCNT concentration. The shapes of the dilatometric curves of the nanocomposites under study differ significantly for the radial and longitudinal directions of the samples. DSC results show that MWCNTs weekly influence calorimetry data, while Raman spectra show that the I D/ I G ratio decreases when MWCNT concentration increases. The IR spectra demonstrate improvement of the crystallinity of the samples as the content in MWCNTs rises.

  18. Stress crack testing of polyethylene geomembranes

    NASA Astrophysics Data System (ADS)

    Halse, Y. H.; Koerner, R. M.; Lord, A. E., Jr.

    The sensitivity of high density polyethylene (HDPE) geomembranes to stress cracking is evaluated under accelerated conditions at a constant stress. The test specimens are in accordance with ASTM D-1822, and are of the dumbbell shape with a constant length in the central section. The accelerated testing conditions consist of a 10 percent Igepal wetting solution in tap water, at a constant temperature of 50 C. The applied stresses are from 30 to 50 percent of the yield stress. It was found that most commercially available HDPE sheet material performs quite well in this type of test. Only one specimen in 80 showed any evidence of cracking and this may have been caused by other reasons. Testing of field fabricated seams, however, resulted in relatively large numbers of cracked specimens. Many of these test specimens showed signs of overgrinding and/or overheating. The results indicate that great care and excellent workmanship are required in the field fabrication of HDPE seams.

  19. Renewable polyethylene mimics derived from castor oil.

    PubMed

    Türünç, Oĝuz; Montero de Espinosa, Lucas; Meier, Michael A R

    2011-09-01

    An increasing number of reports on the syntheses of carbohydrate- and plant oil-based polymers has been published in ongoing efforts to produce plastic materials from renewable resources. Although many of these polymers are biodegradable and this is a desirable property for certain applications, in some cases non-degradable polymers are needed for long-term use purposes. Polyolefins are one of the most important classes of materials that have already taken their places in our daily life. On the other hand, their production relies on fossil resources. Therefore, within this contribution, we discuss synthetic routes toward a number of polyethylene mimics derived from fatty acids via thiol-ene and ADMET polymerization reactions in order to establish more sustainable routes toward this important class of polymers. Two different diene monomers were thus prepared from castor oil derived platform chemicals, their polymerization via the two mentioned routes was optimized and compared to each other, and their thermal properties were investigated.

  20. Viscoplastic tearing of polyethylene thin film

    NASA Astrophysics Data System (ADS)

    Hegyi, Dezso; Pellegrino, Sergio

    2015-05-01

    Recent advances in noncontact strain measurement techniques and large-strain constitutive modeling of the linear low-density polyethylene film used in NASA superpressure balloons StratoFilm 420 are combined to provide a novel measurement technique for the tear propagation critical value of the J-integral. Previously these measurements required complex test configurations and procedures. It is found that the critical value of the J-integral increases by approximately 50 % when the strain rate is decreased from 1.33×10-4 s-1 to 1.33×10-5 s-1. It is shown that there is good correlation between measurements made on uniaxially loaded dogbone samples and circular diaphragms loaded by pressure, both with a 2-mm-wide slit in the middle. This result indicates that more extensive studies of strain-rate dependence may be made with the simpler, uniaxial test configuration.