2021
DOI: 10.1016/j.polymdegradstab.2020.109420
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Characterising plasticised cellulose acetate-based historic artefacts by NMR spectroscopy: A new approach for quantifying the degree of substitution and diethyl phthalate contents

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Cited by 14 publications
(13 citation statements)
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“…PyGCMS of a sample of plastic taken from the degraded hip joint plastic of CA doll C13 identified diethyl phthalate (DEP) and triphenyl phosphate (TPP) (see S.I. Figure S6 and Table S5 ), both of which are commonly encountered external plasticisers in CA artefacts [ 48 ], with TPP also having flame retardant properties [ 26 , 27 ]. CA doll C13 also had distinct needle-shaped white crystalline efflorescence visible on the hands (see Figure 4 below).…”
Section: Resultsmentioning
confidence: 99%
“…PyGCMS of a sample of plastic taken from the degraded hip joint plastic of CA doll C13 identified diethyl phthalate (DEP) and triphenyl phosphate (TPP) (see S.I. Figure S6 and Table S5 ), both of which are commonly encountered external plasticisers in CA artefacts [ 48 ], with TPP also having flame retardant properties [ 26 , 27 ]. CA doll C13 also had distinct needle-shaped white crystalline efflorescence visible on the hands (see Figure 4 below).…”
Section: Resultsmentioning
confidence: 99%
“…Instrumental analysis allows identifying and characterising the different plastic components in artefacts, comprising polymeric blends, and additives (including dyes and pigments). Further, additives may migrate from the polymeric material and degrade at different rates compared to bulk polymers, and being able to identify and quantify them has proven to be extremely informative [ 26 ]. Molecular weight distributions and polymer microstructure affect physical properties and also plastic stability and degradability; therefore, quantitative analyses of such features can lead to more informed preservation strategies in collections [ 27 , 28 ].…”
Section: Identification and Compositional Analysis Of Plastics In mentioning
confidence: 99%
“…Alternatively, 1 H and 13 C NMR spectroscopy is a very useful method for DS determination as it is a direct, nondestructive method and applicable to a broad range of cellulose derivatives. [10][11][12][13][14][15][16][17][18][19][20][21] One of the main limitations of this method is the necessity for solubilization, which is especially challenging for cellulose derivatives with a low DS, which are often insoluble in common organic solvents. Furthermore, it is limited to cellulose derivatives with substituents that show signals in the 1 H NMR spectrum that do not overlap with those of the AGU protons that are typically used as reference for DS calculations.…”
Section: Introductionmentioning
confidence: 99%