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008 150108t2014 my a f m 000 0 eng d
020 _aTHE0004473(Local)
039 9 _a201905161617
_brohana
_c201712051639
_dhuda
_y201501081616
_zfawwaz
040 _aUMP
090 _aTP248.27.M53 A85 2014 r Bc.
100 0 _aNurul Atiqah Abdul Hamid
245 1 0 _aSynthesis of molecularly imprinted polymer for glucose binding /
_cNurul Atiqah Abdul Hamid
260 _aKuantan, Pahang :
_bUMP,
_c2014
300 _axi, 35 p. :
_bill. ;
_c30 cm. +
_e1 CD-ROM
500 _aFaculty of Chemical & Natural Resources Engineering
502 _aProject paper (Bachelor of Chemical Engineering) -- Universiti Malaysia Pahang – 2014
504 _aBibliography : p. 28-30
520 3 _aMolecularly imprinted polymer (MIP) is an attractive technique for the synthesis of highly selective polymeric receptors having artificial generated recognition sites. These materials were synthesized with polymerizable functional monomers and crosslinker that were surrounded around the template molecule. After polymerization, a template molecule was removed leaving in the polymer selective recognition sites with shape, size and functionalities complementary to the template. This study presents a synthesis of MIP selectively for glucose binding. Glucose phosphate salt (GPS) was used as a template molecule with poly(allylamine hydrochloride) (PAA.HCl) as a functional monomer. Three types of crosslinkers which are epichlorohydrin (EPI), ethylene glycol diglycidyl ether (EDGE) and glycerol diglycidyl ether (GDE) were studied during the MIP synthesis. MIP prepared using EPI as a crosslinking showed the highest glucose binding capacity around 0.84 mg glucose/mg dried gel. The binding capacity of MIP prepared using EGDE and GDE are 0.78 mg glucose/mg gel and 0.38 mg glucose/mg gel respectively. It is also found that the increase on GPS monomer concentration will contribute to increase in glucose binding
650 0 _aFermentation
650 0 _aGlucose
856 4 0 _uhttp://ecollib.ump.edu.my/18392/
_zAccess in library only
999 _aVIRTUA40
_c5298
_d5304
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