2019
DOI: 10.1016/j.mtcomm.2019.100678
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Grafting of poly(methacrylic acid-co-acrylamide) film on silicon surface via a simultaneous hydrolysis process

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Cited by 4 publications
(4 citation statements)
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“…In Figure (b), the core-level N 1s behavior is depicted with the divided components of N–H (401.27 eV), N–O (402.62 eV), and N–H 2 (400.19 eV) corresponding to MIP immobilized with the serotonin template. The assigned N–H and N–H 2 components at 401.27 and 400.19 eV, respectively, were found to have originated from our targeted biomolecule 5-HT, whereas the assigned N–O (402.62 eV) along with the N–H (401.27 eV) peak had its source in the AM monomer present in our synthesized polymer. , However, in Figure (c), the N 1s spectrum exhibits two peaks of N–H and N–O along with the emergence of a novel feature N*, which proves the removal of the template molecule 5-HT from the MIP structure. The occurrence of the above feature (marked with *) evidenced at low binding energy is most likely to happen due to the deprotonation of the few N–H bonds.…”
Section: Resultsmentioning
confidence: 76%
“…In Figure (b), the core-level N 1s behavior is depicted with the divided components of N–H (401.27 eV), N–O (402.62 eV), and N–H 2 (400.19 eV) corresponding to MIP immobilized with the serotonin template. The assigned N–H and N–H 2 components at 401.27 and 400.19 eV, respectively, were found to have originated from our targeted biomolecule 5-HT, whereas the assigned N–O (402.62 eV) along with the N–H (401.27 eV) peak had its source in the AM monomer present in our synthesized polymer. , However, in Figure (c), the N 1s spectrum exhibits two peaks of N–H and N–O along with the emergence of a novel feature N*, which proves the removal of the template molecule 5-HT from the MIP structure. The occurrence of the above feature (marked with *) evidenced at low binding energy is most likely to happen due to the deprotonation of the few N–H bonds.…”
Section: Resultsmentioning
confidence: 76%
“…The use of gamma rays as an energy source is a less harmful, less toxic, and more sustainable option for the planet because the preparation, reaction time, and chemical waste are reduced [24]. Therefore, producing high-quality and pure materials is of utmost importance to meet the worldwide demand for disposables and biomedical devices [25].…”
Section: Introductionmentioning
confidence: 99%
“…The following study focuses on the grafting of bioactive polymers bearing carboxylate groups such as polyacrylic acid (PAAc) and methacrylic acid (PMAc) and their chemical and mechanical characterizations. These compounds are chosen as non-toxic, biocompatible and hydrophilic polymers [10,[36][37][38][39][40][41][42]. These bioactive polymers are also very reactive [43], they have the ability to form strong bonds with various materials and are also used as surgical adhesives [44].…”
Section: Introductionmentioning
confidence: 99%