2011
DOI: 10.1002/app.34318
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Melt functionalization of LDPE with thio ester, amino ester, and hydroxy ester by thermolysis method—An FTIR study

Abstract: Low density poly(ethylene) (LDPE) was melt functionalized with three different esters namely, thio ester, amino ester, and hydroxy ester under inert atmosphere at 160 C with different experimental conditions. During the functionalization reaction, crosslinking (C.L) and C¼ ¼C formation are the simultaneous competitive reactions. FTIR-RI analysis method was used to determine the % functionalization onto LDPE backbone and the order of functionalization reaction. Thermogravemetric analysis (TGA) and Differential … Show more

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Cited by 4 publications
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“…The peaks at 1590–1607 (Figure B) and 1578 cm –1 (Figure C) are assigned to the adsorbed acetate v as (COO) species. ,, The peaks from 1681 to 1714 cm –1 (Figure C) and 1672 cm –1 (Figure B) can be assigned to the acetone v (CO) stretching mode . The bands at 1737 cm –1 (Figure B) and 1720–1730 cm –1 (Figure A) are likely due to the absorption of the carbonyl group with the aliphatic ester function υ (CO). , The band at 1650 cm –1 (Figure A) is in agreement with the bicarbonate v as (OCO – ) species stretching bond. , The enolate species (CH 2 CH–O) exhibit bands at 1636, 1653, and 1400 cm –1 (Figure C). , The band at 1591 cm –1 is consistent with the absorption of the formate v as (COO) species (Figure A). The peaks at 1464 (Figure A) and 1470 cm –1 (Figure B) are attributed to the adsorbed methoxy δ as (CH 3 ) groups. , The bands at 1500, 1532, and 1256 cm –1 (Figure C), 1544 (Figure B), and 1549 cm –1 (Figure A) are most likely attributed to v as (COO) and v s (OCO) monodentate carbonate species .…”
Section: Results and Discussionmentioning
confidence: 96%
“…The peaks at 1590–1607 (Figure B) and 1578 cm –1 (Figure C) are assigned to the adsorbed acetate v as (COO) species. ,, The peaks from 1681 to 1714 cm –1 (Figure C) and 1672 cm –1 (Figure B) can be assigned to the acetone v (CO) stretching mode . The bands at 1737 cm –1 (Figure B) and 1720–1730 cm –1 (Figure A) are likely due to the absorption of the carbonyl group with the aliphatic ester function υ (CO). , The band at 1650 cm –1 (Figure A) is in agreement with the bicarbonate v as (OCO – ) species stretching bond. , The enolate species (CH 2 CH–O) exhibit bands at 1636, 1653, and 1400 cm –1 (Figure C). , The band at 1591 cm –1 is consistent with the absorption of the formate v as (COO) species (Figure A). The peaks at 1464 (Figure A) and 1470 cm –1 (Figure B) are attributed to the adsorbed methoxy δ as (CH 3 ) groups. , The bands at 1500, 1532, and 1256 cm –1 (Figure C), 1544 (Figure B), and 1549 cm –1 (Figure A) are most likely attributed to v as (COO) and v s (OCO) monodentate carbonate species .…”
Section: Results and Discussionmentioning
confidence: 96%