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| 003 | MY-KuUP | ||
| 005 | 20260420185027.0 | ||
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| 008 | 260420t20252025my a|||fr|||| 000 0 eng d | ||
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_aTHE0010483 (Local) _qHardback |
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_aUMPSA _beng _cUMPSA _erda |
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| 090 | _aFIST .S95 2025 r Bc. | ||
| 100 | 1 |
_aPeggy, Ngu Shi Ying, _eauthor. |
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| 245 | 1 | 0 |
_aSynthesis and characteristics of biobased epoxy from vanillin / _cPeggy Ngu Shi Ying |
| 264 | 1 |
_aKuantan, Pahang : _bUMPSA, _c2025 |
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| 264 | 4 | _c© 2025 | |
| 300 |
_axii, 52 pages : _billustrations ; |
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_2rdacontent _atext |
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_2rdamedia _aunmediated |
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_2rdacarrier _avolume |
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_2rda _atext file _bPDF |
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| 500 | _aFaculty of Industrial Sciences and Technology | ||
| 502 | _aFinal Year Report (Bachelor of Applied Science of Industrial Chemistry) -- Universiti Malaysia Pahang Al-Sultan Abdullah - 2025 | ||
| 504 | _aInclude bibliographical reference | ||
| 520 | 3 | _aIn this research, there are three objectives needed to be achieved which are investigation of percentage yield of divanillin and chemical structure of vanillin and divanillin, the synthesis process of vanillin-based epoxies by differentiate their curing time, and the study the chemical structure and solvent resistance of vanillin-based epoxies which cured for different duration. In the synthesis process, heating process, and gravity filtration is the major method to get the synthesized products which are divanillin and epoxidized divanillin. The percentage yield of divanillin is calculated by using theoretical and actual yield. Comparison between vanillin and divanillin are studied through carbon-13 Nuclear Magnetic Resonance (NMR) Spectra. The curing time of the vanillin-based epoxy resins are categorized into 1 hour and 2 hours to find out its solvent resistance to four distinct solvents. Fourier Transform Infrared Spectroscopy in Attenuated total reflectance (ATR-FTIR) is used to investigate the possible functional groups in the EDV/IPDA epoxy. In conclusion, there are similarity and difference between vanillin and divanillin due to divanillin is the synthesized product of vanillin. ATR-FTIR method in the wavenumber range of 400-4000 cm-1 can recognize the key functional groups of the epoxidized divanillin (EDV) such as epoxy groups which indicated the successfully cured process in of the EDV/IPDA epoxy. Solvent resistance of the EDV/IPDA with longer curing time is more excellent due to the crosslinking network structure is more rigid and tight than the crosslinking network structure of EDV/IPDA with 1 hour curing time. These results in these experiments provide valuable insights into the synthesis process, chemical structure, solvent resistance, and percentage yield of synthesized products. | |
| 610 | 2 | 0 |
_aFaculty of Industrial Sciences and Technology _xDissertations |
| 650 | 0 |
_aUniversities and colleges _xDissertations |
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| 856 | _uhttps://umpir.ump.edu.my/id/eprint/46119 | ||
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_2lcc _cPSM |
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_c104761 _d104767 |
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