TY - JOUR A1 - Tan, Yi A1 - Wachtendorf, Volker A1 - Kukofka, Tobias A1 - Klack, Patrick A1 - Ruder, J. A1 - Lin, Xuebao A1 - Schartel, Bernhard T1 - Degradation of flame retardance: A comparison of ethylene‐vinyl acetate and low‐density polyethylene cables with two different metal hydroxides JF - Journal of Applied Polymer Science N2 - The durability of flame retardancy is a challenge for cables over long lifetimes. The degradation of flame retardance is investigated in two kinds of exposures, artificial weathering and humidity. In this basic study, typical mineral flame retardants in two polymers frequently used in cable jackets are investigated to get the fundamental picture. Aluminum hydroxide (ATH) and magnesium hydroxide (MDH) are compared in ethylene‐vinyl acetate (EVA), and further in EVA and linear low‐density polyethylene (LLDPE) cables containing the same ATH. The changes in chemical structure at the surface are studied through attenuated total reflectance Fourier transform infrared spectroscopy (ATR‐FTIR), the formation of cracks, and changes in color are investigated. The cone calorimeter and a bench scale fire testing cable module are utilized to evaluate the fire behavior of the cables. Although the flame retardancy deteriorated slightly, it survived harsh exposure conditions for 2000 h. Compared to EVA/MDH and LLDPE/ATH, the fire behavior of EVA/ATH is the least sensitive. Taken together, all of the results converge to estimate that there will be no problem with flame retardancy performance, for materials subjected to natural exposure for several years; the durability of fire retardancy is questionable for longer periods, and thus requires further investigation. KW - Durability KW - Flame retardant KW - Aluminum hydroxide (ATH) KW - Magnesium hydroxide KW - Ethylene-vinyl acetate KW - Cables KW - Weathering PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-519573 DO - https://doi.org/10.1002/app.50149 VL - 138 IS - 14 SP - 50149 PB - Wiley AN - OPUS4-51957 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bandow, Nicole A1 - Will, Verena A1 - Wachtendorf, Volker A1 - Simon, Franz-Georg T1 - Contaminant release from aged microplastic JF - Environmental Chemistry N2 - Recycled plastic granules of high-density polyethylene, polyvinyl chloride and polystyrene the size of microplastics were exposed to artificial aging conditions (2000 h; photooxidative and thermo-oxidative) to simulate their fate outdoors. Their potential to leach into water during the aging process was investigated using column percolation tests. Aging-related changes on the surface of the material were characterised by IR measurements indicating oxidation reactions with the formation of new adsorption bands (C=O, C–O and OH), especially in the case of photooxidative aging. These findings were confirmed by the identification of leachable organic compounds. Leaching of total organic carbon, Cl, Ca, Cu and Zn is clearly affected by changes due to aging, and their release is increased after photooxidative aging. In general, exposure to photooxidative conditions shows a greater influence on aging and thus on leaching and seems to be the more important mechanism for the aging of microplastic in the environment. Comparison with the total content of inorganic species revealed that, for most elements, less than 3% of the total content is released after 2000 h of photooxidative aging. KW - Column percolation tests KW - Heavy metals KW - Photo-oxidation KW - Thermo-oxidation PY - 2017 DO - https://doi.org/10.1071/EN17064 SN - 1448-2517 SN - 1449-8979 VL - 14 IS - 6 SP - 394 EP - 405 AN - OPUS4-43222 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Geburtig, Anja A1 - Wachtendorf, Volker A1 - Falkenhagen, Jana T1 - Combined impact of UV radiation and nitric acid on high‐density polyethylene containers as a laboratory test JF - Packaging Technology and Science N2 - In a laboratory test, transparent high‐density polyethylene (HDPE) jerrycans have been exposed to both UV radiation and 55 wt‐% nitric acid solution at (41 ± 2)°C, for up to 20 days. For comparison, UV radiant exposure (21 days) and nitric acid exposure (up to 6 weeks) were performed separately, at nearly equal temperatures. The damages are compared with FTIR spectroscopy in ATR and HT‐gel permeation chromatography(GPC) on a molecular level and with hydraulic internal pressure testing as a component test. For the used jerrycans, relevant oxidation can only be found after the combined exposure. This is caused by the decomposition of nitric acid into nitrous gases by UV radiation, which is also observed at lower concentrations (28 wt‐%). After 6 days of laboratory exposure, this is rated as critical, which corresponds to about 1/10 year in Central Europe, according to the UV radiant exposure. The gradual increase in oxidative damage shows the reproducibility of the test. KW - Molecular mass distribution KW - High-density polyethylene KW - Nitric acid KW - UV radiation PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-550141 DO - https://doi.org/10.1002/pts.2673 SN - 0894-3214 SP - 1 EP - 7 PB - John Wiley & Sons Ltd AN - OPUS4-55014 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Geburtig, Anja A1 - Wachtendorf, Volker A1 - Schmidt, Anita A1 - Goedecke, Thomas T1 - Combined impact of UV radiation and nitric acid on HDPE containers during outdoor exposure T1 - Kombinierte Einwirkung von UV-Strahlung und Salpetersäure auf HDPE-Behälter bei der Freibewitterung JF - Materials Testing N2 - Unpigmented HDPE jerrycans filled with nitric acid (55%) and water respectively had been exposed to outdoor conditions for one Berlin summer season. As both liquids underwent equal temperature progression, exposure effects of UV radiation and nitric acid as well as of their combination can be separated and compared. On the basis of various property changes after these exposures, synergistic action is evaluated and compared to a damaged Intermediate Bulk Container (IBC) from a transport accident. It is found that carbonyl formation goes along with lightness increase in color measurement due to microcracking and with a worsening in mechanical behavior, all of them showing synergistic effects of UV and nitric acid exposure. In contrast, embedding nitrogen compounds goes along with yellowing of the material but cannot be correlated to oxidation. The reason for intensified damaging is the decomposition of the 55-percent nitric acid and formation of nitrogen oxides even at ambient temperatures, caused by UV radiation. Thus, damaging effects become similar to those caused by fuming nitric acid exposure at temperatures above 60 °C, with the result of strong oxidative degradation of the polyethylene. In contrast, exclusive exposure to the 55-percent nitric acid at 40 °C does not cause any failure. It can therefore be assumed that also the damaged IBC had been exposed to both UV radiation and nitric acid, probably outdoors. KW - Polyethylene KW - Nitric acid KW - UV radiation KW - Outdoor weathering KW - Resistance PY - 2018 DO - https://doi.org/10.3139/120.111148 SN - 0025-5300 VL - 60 IS - 3 SP - 257 EP - 264 PB - Carl Hanser Verlag CY - München AN - OPUS4-44567 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Geburtig, Anja A1 - Goedecke, Thomas A1 - Wachtendorf, Volker T1 - Combined impact of ultraviolet and chemical fluids on high-density polyethylene packaging material JF - Packaging technology & science N2 - To investigate the ageing behaviour of filled plastic containers outdoors, square cuts of the wall of two high-density polyethylene (HDPE) types were exposed to ultraviolet (UV) radiation at their front side and to specific liquid chemicals (de-ionized water, surfactant or White Spirit) at their back. The UV radiant exposure at the front side was 80 MJ/m². To compare the actions of the different exposures, separate dark backside fluid exposures were performed, in parallel. Besides, UV weathering was carried out until a UV radiant exposure of 325 MJ/m², being roughly comparable to outdoor exposure of one year in Northern Australia. An unpigmented HDPE included in the investigation gave no sufficient protection for the White Spirit. In addition, it showed clear degradation after several of these exposures. In combination with the White Spirit, an increase of carbonyl bonds was measured, presumably assignable to degradation products of the White Spirit. For a pigmented HDPE material, with the implemented combined exposures, no relevant damage was observed, within applied the exposure period. KW - Weathering KW - UV KW - HDPE KW - Packaging PY - 2012 DO - https://doi.org/10.1002/pts.959 SN - 0894-3214 VL - 25 IS - 1 SP - 53 EP - 61 PB - Wiley CY - Chichester, UK AN - OPUS4-25417 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Appajaiah, Anilkumar A1 - Wachtendorf, Volker A1 - Daum, Werner T1 - Climatic exposure of polymer optical fibers: Thermooxidative stability characterization by chemiluminescence JF - Journal of applied polymer science N2 - The optical transmission stability was investigated for commercially available polymer optical fibers (POFs) which were exposed to a climate of 92°C and 95% relative humidity for about 3300 h. The optical transmission stability of POFs was correlated to their thermooxidative stability. POFs possessed identical core material, poly(methyl methacrylate), but they differed in the materials used for the claddings. The optical transmission was measured online using a prototype device called multiplexer. The chemiluminescence (CL) technique was applied to characterize the thermooxidative stability and degradation of POFs. CL analysis reveals the thermooxidative degradation of bare POFs (core and cladding), predominantly of the claddings, as a result of climatic exposure. Ultraviolet-visible transmittance measurements demonstrated more changes in the claddings as compared to the cores due to degradation. The CL and optical measurements data indicated that the optical transmission stability of POFs was dependent mainly on the thermooxidative stability of the claddings and their chemical compositions. KW - Ageing KW - Polymer optical fiber KW - Degradation KW - Chemiluminescence KW - Transparency PY - 2007 DO - https://doi.org/10.1002/app.23955 SN - 0021-8995 SN - 1097-4628 VL - 103 IS - 3 SP - 1593 EP - 1601 PB - Wiley InterScience CY - Hoboken, NJ AN - OPUS4-19072 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schartel, Bernhard A1 - Krüger, Simone A1 - Wachtendorf, Volker A1 - Hennecke, Manfred T1 - Chemiluminescence: A promising new testing method for plastic optical fibers JF - Journal of lightwave technology N2 - The thermo-oxidative degradation of a polymeric optical cable is investigated by chemiluminescence, The results are reliable and reproducible. Two distinct processes are reported marked by a peak and a plateau behavior versus the time, respectively. Both processes are ruled by thermally activated processes. Beside the dependencies of temperature and time, the influence of absorbed water is discussed. Chemiluminescence is proposed as a promising candidate for a suitable testing method assessing the thermo-oxidative stability of plastic optical fibers and cables. it requires not more than a simple one-day testing procedure and has the advantage that it can be carried out even within the lo cv temperature ranges of the cables' intended use. KW - Chemiluminescence KW - Chemilumineszenz PY - 1999 DO - https://doi.org/10.1109/50.803022 SN - 0733-8724 SN - 1558-2213 VL - 17 IS - 11 SP - 2291 EP - 2296 PB - Institute of Electrical and Electronics Engineers CY - New York, NY AN - OPUS4-718 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wachtendorf, Volker A1 - Geburtig, Anja T1 - Chemiluminescence for the early detection of weathering effects of coatings - Part II: Experimental set-up and examination JF - JCT coatingsTech KW - Chemiluminescence KW - Weathering KW - Polymer KW - Oxidation PY - 2010 SN - 1547-0083 VL - 7 IS - 5 SP - 38 EP - 44 PB - Federation of Societies for Coatings Technology CY - Blue Bell, Pa. AN - OPUS4-21494 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wachtendorf, Volker A1 - Geburtig, Anja T1 - Chemiluminescence for the early detection of weathering effects of coatings - Part I: Fundamentals JF - JCT coatingsTech KW - Chemiluminescence KW - Weathering KW - Polymer KW - Oxidation PY - 2010 SN - 1547-0083 VL - 7 IS - 4 SP - 66 EP - 71 PB - Federation of Societies for Coatings Technology CY - Blue Bell, Pa. AN - OPUS4-21493 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Appajaiah, Anilkumar A1 - Wachtendorf, Volker A1 - Daum, Werner T1 - Characterization of thermo-oxidative stability of polymer optical fibers using chemiluminescence technique JF - Polymer degradation and stability N2 - The thermo-oxidative stability of commercially available polymer optical fibers (POFs) and their components (cores and claddings) was investigated. All the bare POFs (core and cladding only) studied here were based on poly(methyl methacrylate) (PMMA) core. The fibers were exposed to 100 °C/low humidity for about 4200 h. Chemiluminescence (CL) technique was applied to investigate the thermo-oxidative stability and for measuring the transmission loss during exposure a prototype device called multiplexer was used. POFs exhibited variation in thermo-oxidative stability although they possessed identical core material PMMA. This was due to difference in the chemical compositions of claddings. Claddings were more susceptible to the thermo-oxidative degradation compared to cores. The thermo-oxidative degradation of both the cladding and the core was found in POFs as a result of climatic exposure. POFs showed an early drop-off followed by a slow decline of transmission. The early drop-off of transmission was attributed to physical changes like thermal expansion and the slow decline of transmission to chemical changes like oxidative degradation of POFs. A good linear relationship between optical transmission stability and thermo-oxidative stability of POFs was established from these studies. KW - Polymer optical fibers (POFs) KW - Chemiluminescence (CL) KW - Thermo-oxidative stability KW - Aging KW - Optical transmission stability PY - 2006 DO - https://doi.org/10.1016/j.polymdegradstab.2006.05.006 SN - 0141-3910 SN - 1873-2321 VL - 91 IS - 11 SP - 2605 EP - 2613 PB - Applied Science Publ. CY - London AN - OPUS4-13984 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -