scholarly journals Are agricultural plastic covers a source of plastic debris in soil? A first screening study

2021 ◽  
Author(s):  
Zacharias Steinmetz ◽  
Paul Löffler ◽  
Silvia Eichhöfer ◽  
Jan David ◽  
Katherine Muñoz ◽  
...  

Abstract. Agricultural plastic covers made from polyethylene (PE) and polypropylene (PP) offer increased yields and an improved crop quality. However, such covers are suspected of partially breaking down into smaller debris and thereby contributing to soil pollution with microplastics. To scrutinize this, we randomly sampled 240 topsoil cores (0–5 cm) from eight fields covered with fleeces, perforated foils, and plastic mulches for less than two years. Samples from the field periphery (50 m perimeter) served as reference. Visual plastic debris > 2 mm was analyzed by Fourier transformed infrared spectroscopy with attenuated total reflection (FTIR–ATR). Smaller, soil-associated plastic debris was dispersed from 50 g of fine soil (≤ 2 mm) using sodium hexametaphosphate solution and density-separated with saturated NaCl solution. The collected PE, PP, and polystyrene (PS) debris was selectively dissolved in a mixture of 1,2,4-trichlorobenzene and p-xylene at 150 °C and quantified by pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). We counted six PE and PS fragments > 2 mm in two out of eight fields. By contrast, Py-GC/MS analysis revealed PE, PP, and PS contents > 1 µg g−1 in seven fields (17 % of all samples). In three fields, PE levels of 3–35 µg g−1 were associated with the use of thinner and less durable perforated foils (40 µm thickness). This was slightly more pronounced at field edges where the plastic covers are turned and weighted down. By contrast, 50 µm thick PE films were not indicated to emit any plastic debris. PP contents of 5–10 µg g−1 were restricted to single observations in the field centers of three sites. On one site, we found expanded PS particles >2 mm that concurred with elevated PS levels (8–19 µg g−1) in the fine soil. Both PP and PS were distributed indistinctly across sites so that their source remained unresolved. In addition, the extent to which plastic contents of up to 7 µg g−1 in the field periphery of some sites were attributed to wind drift from the covered fields or from external sources needs to be investigated in future studies. Yet, our results suggest that the short-term use of thicker and more durable plastic covers should be preferred to limit plastic emissions and accumulation in soil.

2019 ◽  
Author(s):  
Zacharias Steinmetz ◽  
Aaron Kintzi ◽  
Katherine Muñoz ◽  
Gabriele E. Schaumann

The lack of adequate analytical methods for the quantification of plastic debris in soil challenges a better understanding of their occurrence and fate in the terrestrial environment. With this study, we developed and validated a simple and fast method for the selective quantification of the three most environmentally relevant polymers polyethylene (PE), polypropylene (PP), and polystyrene (PS) in soil using pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). In order to facilitate the preparation of calibration series and to better account for the heterogeneity of soil matrix, polymers were dissolved in 1,2,4-trichlorobenzene (TCB) at 120 °C. Thereby, liquid sample aliquots from up to 4 g of solid sample became amenable to pyrolysis without further preparation. To evaluate the performance of this approach, three reference soils with 1.73–5.16 % organic carbon (Corg) were spiked at 50 and 250 μg g−1 of each polymer and extracted with TCB. A prior cleanup step with methanol, flocculation with KAl(SO4)2, and Fenton digestion were tested for their suitability to reduce potentially interfering Corg. Calibration curves responded linearly (adj. R2 > 0.996) with instrumental detection limits of 1–86 ng corresponding to method detection limits of 1–86 μg g−1. The measurement repeatability was 3.2–7.2 % relative standard deviation. The best recoveries (70–128 %) were achieved for plastic contents of 250 μg g−1 extracted with TCB without prior cleanup from soils with less than 2.5 % Corg. A higher Corg particularly interfered with the quantification of PE. The addition of non-target polymers (polyethylene terephthalate, polyvinyl chloride, poly(methyl methacrylate), and tire wear particles) did not interfere with the quantification of the analytes highlighting the selectivity of the method. Further research is needed to determine low plastic contents in soils exceeding 2.5 % Corg. With less than 3 h processing time per sample, our method is particularly suitable for routine analyses and screening studies of agricultural systems to be complemented with microspectroscopic techniques for additional information on particle shapes and sizes.


Polymers ◽  
2021 ◽  
Vol 14 (1) ◽  
pp. 121
Author(s):  
Till Krieg ◽  
Cristian Mazzon ◽  
Elena Gómez-Sánchez

Identifying the most vulnerable plastics and monitoring their deterioration is one of the main problems within heritage collections with historical synthetic polymers. Gathering and interpreting data about material and degradation phenomena in a collection reveals its conservation needs. A systematic survey of the collection can help towards this purpose. Surveys aiming at inspecting and documenting damages rely on several tools in order to fulfill their purpose. Firstly, objective descriptions of the damages that may appear, and secondly, the means of acquiring and interpreting material information. To address these needs, this article presents (a) a visual damage catalogue of degradation phenomena in plastic and rubber materials, and (b) the implementation of Fourier-transform infrared spectroscopy (FTIR) and pyrolysis–gas chromatography–mass spectrometry (py-GCMS) for the identification of analytically challenging rubber materials and of blooming phenomena. The damage catalogue is based solely on visual and olfactory signs, so that the assessment is independent of possible causes of damages and underlying processes, with the purpose of allowing objectivity to prime over interpretation. The limitations of the use of FTIR in the identification of heavily compounded rubbers in museum surveys is highlighted, and examples are presented. The use of py-GCMS on these cases conveniently allowed the identification of the constituting monomers of several rubber materials where FTIR could not provide a univocal classification of the material present. The study of several cases of blooming allowed the identification of diverse compositions and origins, showing that the description of a degradation phenomenon is only the first step towards its understanding. Unveiling the nature of a particular case of blooming is particularly critical when conservation treatments, such as the removal of a (potentially protecting) layer, are planned. For this purpose, attenuated total reflection-FTIR (ATR-FTIR) as a surface technique was particularly useful.


Materials ◽  
2019 ◽  
Vol 12 (12) ◽  
pp. 1946 ◽  
Author(s):  
Qilan Fu ◽  
Alain Cloutier ◽  
Aziz Laghdir ◽  
Tatjana Stevanovic

The aim of this study was to investigate the effects of heat and steam on the chemical properties of thermo-hygromechanical (THM)-densified sugar maple wood. The THM densification process was performed at two different temperatures (180 °C and 200 °C) with and without steam. The functional groups, surface chemical composition and internal structure and components of the control and densified samples were investigated using attenuated total reflection Fourier transform infrared (ATR-FTIR), X-ray photoelectron (XPS) spectroscopy and pyrolysis gas chromatography-mass spectrometry (Py-GC/MS). The obtained results suggest that the THM densification treatment resulted in significant chemical changes on the wood surface. The results of the ATR-FTIR spectra confirmed the decomposition of hemicelluloses and the relative increase of cellulose and lignin contents on the wood surface. The Py-GC/MS and XPS results show an increase of the oxygen/carbon atomic (O/C) ratio, which indicated that chemical substances containing oxygenated functionality were formed through the densification process. The densification treatment favored the depolymerization of hemicelluloses and cellulose as indicated by an increased anhydrous sugar (levoglucosan) release during the pyrolysis process. Densification also facilitated the cleavage of the lignin side chains, resulting in increased phenyl units with short chains released during the pyrolysis process.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
H. Lee ◽  
D. Lee ◽  
J. M. Seo

AbstractAlthough there have been many instances of ship collision at sea in recent times, not much research has been conducted on the topic. In this study, paint from an actual site of ship collision was collected and analyzed as evidence. The amount of evidence collected from the ships involved in the collision is either small or has inconsistent morphology. In addition, the contaminants and samples are often mixed in this evidence, making its analysis difficult. Paint traces of the damaged ship and the ship suspected to be responsible for the collision were compared through scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM–EDS), attenuated total reflection–Fourier transform infrared spectroscopy (ATR–FTIR), thermogravimetry (TG) and derivative thermogravimetry (DTG), and pyrolysis–gas chromatography/mass spectrometry (Py–GC/MS) analyses. The ship responsible for the collision could be identified by characterization and by performing a comparative analysis of the extracted paint. Among the methods used in this study, Py–GC/MS can sensitively analyze even similar paints, and identified styrene and phthalic anhydride as the most prominent components of the paint used as evidence. The results obtained can be used to investigate the evidence collected from collision sites and to determine the ship responsible for the collision.


2019 ◽  
Author(s):  
Zacharias Steinmetz ◽  
Aaron Kintzi ◽  
Katherine Muñoz ◽  
Gabriele E. Schaumann

The lack of adequate analytical methods for the quantification of plastic debris in soil challenges a better understanding of their occurrence and fate in the terrestrial environment. With this proof-of-principle study, we developed a simple and fast method for the selective quantification of the three most environmentally relevant polymers polyethylene (PE), polypropylene (PP), and polystyrene (PS) in soil using pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). In order to facilitate the preparation of calibration series and to better account for the heterogeneity of soil matrix, polymers were dissolved in 1,2,4-trichlorobenzene (TCB) at 120 °C. Thereby, liquid sample aliquots from up to 4 g of solid sample became amenable to pyrolysis without further preparation. To evaluate the performance of this approach, three reference soils with 1.73–5.16 % organic carbon (Corg) were spiked at 50 and 250 μg g−1 of each polymer and extracted with TCB. A prior cleanup step with methanol, flocculation with KAl(SO4)2, and Fenton digestion were tested for their suitability to reduce potentially interfering Corg. Calibration curves responded linearly (adj. R2 > 0.996) with instrumental detection limits of 1–86 ng corresponding to method detection limits of 1–86 μg g−1. The measurement repeatability was 3.2–7.2 % relative standard deviation. Recoveries of 70–128 % were achieved for plastic contents of 250 μg g−1 extracted with TCB without prior cleanup from soils with less than 2.5 % Corg. A higher Corg particularly interfered with the quantification of PE. The addition of non-target polymers (polyethylene terephthalate, polyvinyl chloride, poly(methyl methacrylate), and tire wear particles) did not interfere with the quantification of the analytes highlighting the selectivity of the method. Further research is needed to determine low plastic contents in soils exceeding 2.5 % Corg. With 1–3 h processing time per sample, our method has the potential for routine analyses and screening studies of agricultural systems to be complemented with microspectroscopic techniques for additional information on particle shapes and sizes.


2019 ◽  
Author(s):  
Zacharias Steinmetz ◽  
Aaron Kintzi ◽  
Katherine Muñoz ◽  
Gabriele E. Schaumann

The lack of adequate analytical methods for the quantification of plastic debris in soil challenges a better understanding of their occurrence and fate in the terrestrial environment. With this proof-of-principle study, we developed a simple and fast method for the selective quantification of the three most environmentally relevant polymers polyethylene (PE), polypropylene (PP), and polystyrene (PS) in soil using pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). In order to facilitate the preparation of calibration series and to better account for the heterogeneity of soil matrix, polymers were dissolved in 1,2,4-trichlorobenzene (TCB) at 120 °C. Thereby, liquid sample aliquots from up to 4 g of solid sample became amenable to pyrolysis without further preparation. To evaluate the performance of this approach, three reference soils with 1.73–5.16 % organic carbon (Corg) were spiked at 50 and 250 μg g−1 of each polymer and extracted with TCB. A prior cleanup step with methanol, flocculation with KAl(SO4)2, and Fenton digestion were tested for their suitability to reduce potentially interfering Corg. Calibration curves responded linearly (adj. R2 > 0.996) with instrumental detection limits of 1–86 ng corresponding to method detection limits of 1–86 μg g−1. The measurement repeatability was 3.2–7.2 % relative standard deviation. Recoveries of 70–128 % were achieved for plastic contents of 250 μg g−1 extracted with TCB without prior cleanup from soils with less than 2.5 % Corg. A higher Corg particularly interfered with the quantification of PE. The addition of non-target polymers (polyethylene terephthalate, polyvinyl chloride, poly(methyl methacrylate), and tire wear particles) did not interfere with the quantification of the analytes highlighting the selectivity of the method. Further research is needed to determine low plastic contents in soils exceeding 2.5 % Corg. With 1–3 h processing time per sample, our method has the potential for routine analyses and screening studies of agricultural systems to be complemented with microspectroscopic techniques for additional information on particle shapes and sizes.


TAPPI Journal ◽  
2017 ◽  
Vol 16 (03) ◽  
pp. 145-152
Author(s):  
Raquel Prado ◽  
Lisa Weigand ◽  
Shikh M.S.N.S. Zahari ◽  
Xabier Erdocia ◽  
Jason Hallett ◽  
...  

Lignin structure elucidation is one of the main targets for biorefinery related research. Because of its complexity, obtaining reproducible results in a straight-forward way is very important. One of the values that is used to compare different lignins is the syringyl:guaiacyl (S/G) ratio, which has been measured in different ways. The most reliable result is obtained for nitrobenzene oxidation, but this involves a complex process. In this work, the S/G ratios measured by pyrolysis-gas chromatography mass spectrometry (py-GCMS) and heteronuclear single quantum coherence-nuclear magnetic resonance (HSQC-NMR) spectroscopy were compared with attenuated total reflection infrared (ATR-IR) spectroscopy results to establish a reliable, quick, and simple method for the measurement. To achieve this, two mathematical models were applied with multivariate data analysis software. A partial least squares regression model for py-GCMS gave the best result.


Author(s):  
Emma Jakab ◽  
Zoltán Sebestyén ◽  
Bence Babinszki ◽  
Eszter Barta-Rajnai ◽  
Zsuzsanna Czégény ◽  
...  

SummaryThe thermo-oxidative decomposition of lovage (Levisticum officinale) and davana (Artemisia pallens) essential oils has been studied by pyrolysis-gas chromatography/mass spectrometry in 9% oxygen and 91% nitrogen atmosphere at 300 °C to simulate low-temperature tobacco heating conditions. Both lovage and davana oils contain numerous chemical substances; the main components of both oils are various oxygen-containing compounds. Isobenzofuranones are the most important constituents of lovage oil, and their relative intensity changed significantly during oxidative pyrolysis. (Z)-ligustilide underwent two kinds of decomposition reactions: an aromatization reaction resulting in the formation of butylidenephthalide and the scission of the lactone ring with the elimination of carbon dioxide or carbon monoxide. Davanone is the main component of davana oil, which did not decompose considerably during low-temperature oxidative pyrolysis. However, the relative yield of the second most intensive component, bicyclogermacrene, reduced markedly due to bond rearrangement reactions. Davana ether underwent oxidation reactions leading to the formation of various furanic compounds. The changes in the composition of both essential oils could be interpreted in terms of bond splitting, intramolecular rearrangement mechanisms and oxidation reactions of several constituents during low-temperature oxidative pyrolysis. The applied thermo-oxidative method was found to be suitable to study the stability of the essential oils and monitor the decomposition products under simulated tobacco heating conditions. In spite of the complicated composition of the essential oils, no evidence for interaction between the oil components was found. [Beitr. Tabakforsch. Int. 29 (2020) 27–43]


2008 ◽  
Vol 6 (1) ◽  
Author(s):  
Markus Heryanto Langsa

<p>Penelitian ini bertujuan untuk menentukan senyawa organik khususnya organic karbon terlarut (DOC) dari dua spesies daun tumbuhan (<em>wandoo eucalyptus </em>and <em>pinus radiate, conifer</em>) yang larut dalam air selama periode 5 bulan leaching eksperimen. Kecepatan melarutnya senyawa organic ditentukan secara kuantitatif dan kualitatif menggunakan kombinasi dari beberapa teknik diantaranya Total Organic Carbon (TOC) analyser, Ultraviolet-Visible (UV-VIS) spektrokopi dan pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS).</p><p>Hasil analisis DOC dan UV menunjukkan peningkatan yang tajam dari kelarutan senyawa organic di awal periode pengamatan yang selanjutnya berkurang seiring dengan waktu secara eksponensial. Jumlah relatif senyawa organic yang terlarut tergantung pada luas permukaan, aktifitas mikrobiologi dan jenis sampel tumbuhan (segar atau kering) yang digunakan. Fluktuasi profil DOC dan UV<sub>254</sub> disebabkan oleh aktifitas mikrobiologi. Diperoleh bahwa daun kering lebih mudah terdegradasi menghasilkan senyawa organic dalam air dibandingkan dengan daun segar. Hasil pyrolysis secara umum menunjukkan bahwa senyawa hidrokarbon aromatic dan fenol (dan turunannya) lebih banyak ditemukan pada residue sampel setelah proses leaching kemungkinan karena adanya senyawa lignin atau aktifitas humifikasi mikrobiologi membuktikan bahwa senyawa-senyawa tersebut merupakan komponen penting dalam proses karakterisasi DOC.</p>


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