2020
DOI: 10.1002/app.49319
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Improvement of the processability and thermal stability of poly(vinyl chloride) with 5,6‐diamino‐1,3‐dimethyluracil

Abstract: Uracil derivatives are potential nontoxic thermal stabilizers of poly(vinyl chloride) (PVC) and have a better stabilization effect. 5,6‐diamino‐1,3‐dimethyluracil (DDU) was investigated as a thermal stabilizer for PVC. The stabilization effect of DDU was measured by thermogravimetric analysis, thermal aging test, and recording the time of the color change of the Congo red paper (Congo red test). Meanwhile, the processability of PVC stabilized by DDU was investigated through dynamic performance test. The result… Show more

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Cited by 9 publications
(10 citation statements)
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“…Figure 3 is the 1 H NMR characterization of AM, 1 H NMR (400 MHz, deuterated DMSO). As shown in Figure 3: chemical shift δ = 2.50 corresponded to the characteristic peak of the solvent deuterated DMSO; chemical shift δ = 6.62 and δ = 6.50 corresponded to 1 hydrogen on carbon–carbon double bond respectively; The singlet at chemical shift δ = 4.68 corresponded to 1 hydrogen on the imino group attached to the carbonyl group; chemical shift δ = 8.08 corresponded to 1 hydrogen on the carbon–carbon double bond in uracil structure; chemical shifts δ = 3.24 and δ = 3.07 [ 10 ] corresponded to the three hydrogens of the two methyl groups on uracil, respectively. According to the structural formula, the corresponding chemical shift parameters were displayed in the molecular structure of the synthesized target product.…”
Section: Resultsmentioning
confidence: 99%
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“…Figure 3 is the 1 H NMR characterization of AM, 1 H NMR (400 MHz, deuterated DMSO). As shown in Figure 3: chemical shift δ = 2.50 corresponded to the characteristic peak of the solvent deuterated DMSO; chemical shift δ = 6.62 and δ = 6.50 corresponded to 1 hydrogen on carbon–carbon double bond respectively; The singlet at chemical shift δ = 4.68 corresponded to 1 hydrogen on the imino group attached to the carbonyl group; chemical shift δ = 8.08 corresponded to 1 hydrogen on the carbon–carbon double bond in uracil structure; chemical shifts δ = 3.24 and δ = 3.07 [ 10 ] corresponded to the three hydrogens of the two methyl groups on uracil, respectively. According to the structural formula, the corresponding chemical shift parameters were displayed in the molecular structure of the synthesized target product.…”
Section: Resultsmentioning
confidence: 99%
“…It can be seen from the TG curve that PVC has two stages of thermal weight loss. [ 10 ] The first stage is in the range of 180 ~ 400°C: the hydrogen chloride is released by thermal decomposition, and the conjugated polyene is gradually formed; the second stage is in the range of 400 ~ 550°C: the long carbon skeleton is broken to generate linear or cyclic low molecular weight hydrocarbons, such as polyene, benzene and other structures. Figure 4 is the TG curve of pure PVC, CaSt 2 /AM‐Zn = 2:1, and CaSt 2 /ZnSt 2 = 2:1 system.…”
Section: Resultsmentioning
confidence: 99%
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“…The thermal stabilizer used in industry now generally consists of a variety of thermal stabilizers. Under the synergistic effect of the main thermal stabilizer, the auxiliary thermal stabilizer has the advantages of small dosage and high efficiency, and has attracted much attention in recent years 9,10 …”
Section: Introductionmentioning
confidence: 99%