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- Biofuels (3)
- Polyethylene grades (3)
- Change in MFR and tensile properties (2)
- Coating (2)
- Compatibility (2)
- NO2 (2)
- Ringversuch (2)
- Spurenverunreinigungen (2)
- ATR-FTIR (1)
- Al2O3 (1)
Organisationseinheit der BAM
- 1 Analytische Chemie; Referenzmaterialien (2)
- 1.4 Prozessanalytik (2)
- 3 Gefahrgutumschließungen; Energiespeicher (1)
- 3.2 Gefahrguttanks und Unfallmechanik (1)
- 4 Material und Umwelt (1)
- 4.5 Kunst- und Kulturgutanalyse (1)
- 5 Werkstofftechnik (1)
- 5.6 Glas (1)
- 7 Bauwerkssicherheit (1)
- 7.6 Korrosion und Korrosionsschutz (1)
IR and Raman study of calcium aluminosilicate glasses of the composition xCaO.xAl2O3.(100-2x)SiO2
(2002)
Delta-Hexabromocyclododecane
(2007)
Improved wetting of bare and pre-coated steels by aqueous alumina sols for optimum coating success
(2010)
Alumina coatings are a promising candidate for
the protection of metals prone to high temperature corrosion.
If applied via sol–gel process, especially by using so
called aqueous modified Yoldas-sols, the deposition is
hardened by differences in surface free energy of substrate
and sol. In this paper the apparent surface properties of
samples to be coated and sols were examined by contact
angle measurements, IR-spectroscopy and tensiometry.
The results imply, after consideration of possible uncertainties,
the use of surface tension reducing 2-butanol
already present during hydrolysis of the sols to obtain an
easy and successful coating process.
The aim of this work was to study the interaction between high density polyethylene (HDPE) grades as material for dangeraus goods packagings and biofuels such as E10 (fuel with 10% ethanol), E85 (fuel with 85% ethanol), biodiesei and 810 (heating oil with 10% biodiesel). Jerricans made of two polyethylene grades were filled with these fuels and exposed to temperatures of 20 oc and 40 oc for more than one year. Tensile properlies (tensile strength, breaking elongation and elasticity modulus) and Melt Flow Rate (MFR) were determined, and Fourier Transform Infrared Spectroscopy (FTIR) was used to evaluate changes in the chemical structure.
Measurements of the MFR and tensile properlies of the polyethylene grades after exposure to E1 0, E85 and 810 showed only a slightly damaging influence. A n increase in the peak of 1585 cm·1 for the (C=C) stretching vibrations was visible in the FTIR spectra after immersion tests with E85. A n increase in the MFR with the immersion time of the grades in biodiesei was measured - in parlicular, after one year of exposure. The elasticity modulus of the polyethylene grades was reduced with the immersion time too. The FTIR spectra showed a broadening of the C=O peak of 1740 cm·1 and the appearance of the hydroxyl group at 3500 cm·1.
8iofuels including ethanol and biodiesel (fatty acid methyl ester) represent an important renewable fuel alternative to petroleum-derived transport fuels. lncreasing biofuels use would bring some benefits, such as a reduction in oil demands and greenhause gas emissions, and an improvement in air quality.
Biofuels including ethanol and biodiesel (FAME) represent a renewable fuel alternative to petroleum-derived transport fuels. The aim of this work was to study the interaction between high density polyethylene (HDPE) with permeation barriers in form of polyamide (PA) and fluorination, and biofuels such as E85 (fuel with 85 % ethanol), biodiesel and B10 (heating oil with 10 % biodiesel). 10 l jerrycans made of polyethylene with permeation barrier of PA were filled with E85 and biodiesel and exposed to temperatures of 20 °C and 40 °C for 5 years. Half of the 20 l jerrycans of HDPE for filling with B10 were fluorinated at the inner layer to prevent permeation before the exposure. Tensile properties were determined once a year, and FTIR-spectroscopy was used to evaluate possible changes.
The tensile properties tensile strength and breaking elongation of HDPE jerrycan cuttings with permeation barrier decreased, but not significantly, after immersion in E85, biodiesel and B10. The elasticity modulus of the polyethylene grades was especially reduced during exposure to E85.
The FTIR spectra of HDPE jerrycan cuttings with permeation barrier showed that immersion tests for five years with the test fuels at 20 °C and 40 °C did not lead to a decomposition of the permeation barriers.
Resistance to oxidative degradation by nitric acid has been selected for a comparison of polyethylene grades in a European standard on suitability proof for alternative plastic resins used for packagings and intermediate bulk containers (IBCs) for the transport of dangerous goods. Measurements of the infrared (IR) absorption spectra of microtome slices cut from the walls of jerricans, which were pre-stored with 55% nitric acid for 21 and 42 days at 40°C, showed changes in the structure of the polyethylene. The penetration depths of 55% nitric acid into the polyethylene grades are, in principle, suitable for evaluating the resistance to oxidative degradation of polyethylene grades after pre-storage of the packagings for 21 days. After this period the packaging wall is not fully penetrated. The intensities of the IR bands at 1565 cm-1 (-NO2), 1630 cm-1 (-C=C) and 1654 cm-1 (-O-NO2) increased with the treatment time with 55% nitric acid as a result of oxidative damage by the nitric acid. The high increase in absorbance of the -C=C band in the region 1630 - 1690 cm-1 is attributable to paraffinic chain cracks. The absorbance of the -O-NO2 band, formed as result of the nitration process was still low at a test temperature of 40°C.
The assessment of quantification results of the alcohol abuse marker ethyl glucuronide (EtG) in hair in comparison to the cut-off values for the drinking behavior may be complicated by cosmetic hair bleaching. Thus, the impact of increasing exposure to hydrogen peroxide on the EtG content of hair was investigated. Simultaneously, the change of absorbance in the range of 1000–1100 cm-1 indicative for the oxidation of cystine was investigated non-destructively by attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) using pulverized portions of the respective hair samples. Hair samples treated with hydrogen peroxide consistently displayed a significantly increased absorbance at 1040 cm-1 associated with the formation of cysteic acid. The EtG content decreased significantly if the hair was treated with alkaline hydrogen peroxide as during cosmetic bleaching. It could be shown that ATR-FTIR is capable of detecting an exposure to hydrogen peroxide when still no brightening was visible and already before the EtG content deteriorated significantly. Thus, hair samples suspected of having been exposed to oxidative treatment may be checked non-destructively by a readily available technique. This assay is also possible retrospectively after EtG extraction and using archived samples.