功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2010年
1期
96-99
,共4页
谭帼馨%阮雄杰%宁成云%关燕霞%田冶
譚幗馨%阮雄傑%寧成雲%關燕霞%田冶
담귁형%원웅걸%저성운%관연하%전야
N-异丙基丙稀酰胺%聚乙二醇双丙烯酸酯%水凝胶%表征%亲水性
N-異丙基丙稀酰胺%聚乙二醇雙丙烯痠酯%水凝膠%錶徵%親水性
N-이병기병희선알%취을이순쌍병희산지%수응효%표정%친수성
NIPAM%PEGDA%hydrogel%characterization%hydrophilicity
采用烯腈烷基化再部分水解的方法合成的N-异丙基丙烯酰胺(NIPAM)单体,并利用红外光谱(FT-IR)、氢核磁共振谱(~1H NMR)、质谱(MS)进行了表征.以IRGACURE2959为光引光剂,通过紫外光引发光聚合的方法合成了PEGDA/NIPAM共聚物水凝胶,并对共聚物进行FT-IR表征,探讨了凝胶的亲水性能.结果表明,NIAPM单体的FT-IR中含1657.7cm~(-1)的羰基峰、1549.5cm~(-1)氨基上的氢峰、1367.5cm~(-1)的异丙基上的振动氢峰和1621.2cm~(-1)的烯烃双键峰,1H NMR中含δH7.9亚胺基的活泼氢峰及双键中同碳位、顺式位和反式位的氢峰及异丙基特征峰,MS表明m/z=112为分子离子峰,结果符合NIPAM结构式;聚合物FT-IR表明,双键的特征峰减弱,双键打开合成了PEGDA/NIPAM共聚物;随着NIPAM单体含量的增大,共聚物的接触角减小,平衡溶胀率增大,亲水性增强.
採用烯腈烷基化再部分水解的方法閤成的N-異丙基丙烯酰胺(NIPAM)單體,併利用紅外光譜(FT-IR)、氫覈磁共振譜(~1H NMR)、質譜(MS)進行瞭錶徵.以IRGACURE2959為光引光劑,通過紫外光引髮光聚閤的方法閤成瞭PEGDA/NIPAM共聚物水凝膠,併對共聚物進行FT-IR錶徵,探討瞭凝膠的親水性能.結果錶明,NIAPM單體的FT-IR中含1657.7cm~(-1)的羰基峰、1549.5cm~(-1)氨基上的氫峰、1367.5cm~(-1)的異丙基上的振動氫峰和1621.2cm~(-1)的烯烴雙鍵峰,1H NMR中含δH7.9亞胺基的活潑氫峰及雙鍵中同碳位、順式位和反式位的氫峰及異丙基特徵峰,MS錶明m/z=112為分子離子峰,結果符閤NIPAM結構式;聚閤物FT-IR錶明,雙鍵的特徵峰減弱,雙鍵打開閤成瞭PEGDA/NIPAM共聚物;隨著NIPAM單體含量的增大,共聚物的接觸角減小,平衡溶脹率增大,親水性增彊.
채용희정완기화재부분수해적방법합성적N-이병기병희선알(NIPAM)단체,병이용홍외광보(FT-IR)、경핵자공진보(~1H NMR)、질보(MS)진행료표정.이IRGACURE2959위광인광제,통과자외광인발광취합적방법합성료PEGDA/NIPAM공취물수응효,병대공취물진행FT-IR표정,탐토료응효적친수성능.결과표명,NIAPM단체적FT-IR중함1657.7cm~(-1)적탄기봉、1549.5cm~(-1)안기상적경봉、1367.5cm~(-1)적이병기상적진동경봉화1621.2cm~(-1)적희경쌍건봉,1H NMR중함δH7.9아알기적활발경봉급쌍건중동탄위、순식위화반식위적경봉급이병기특정봉,MS표명m/z=112위분자리자봉,결과부합NIPAM결구식;취합물FT-IR표명,쌍건적특정봉감약,쌍건타개합성료PEGDA/NIPAM공취물;수착NIPAM단체함량적증대,공취물적접촉각감소,평형용창솔증대,친수성증강.
The synthesis method of pure N-isopropylacrylamide (NIPAM) monomer was studied in this paper,which was alkylated alkene nitrile and then hydrolyzed.The properties of the synthesis monomer was investigated respectively by fourier transform infrared spectroscopy (FT-IR),1H nuclear magnetic resonance (~1H NMR) and mass spectrometry (MS).The co-polymer hydrogels was synthesized by UV-initiated polymerization of poly(ethylene glycol ) diacrylate (PEGDA) and NIPAM,with IRGACURE2959 as an initiator.The polymer was investigated by FT-IR.And the hydrophilicity of the hydrogel was discussed with contact angle and equilibrium water content.The FT-IR showed that,1657.7cm~(-1) was C=O peak,1549.5cm~(-1) was N-H peak,1367.5cm~(-1) was isopropyl C-H peak and 1621.2cm~(-1) was C=C peak.The 1H NMR showed that δH7.9 was the active hydrogen peak of imino and distinguished the hydrogen peak from the gem-position,cis-position and trans-position of double bond.The MS showed that m/z 112 was the molecular ion peak.All of the above results was in line with the structure of NIPAM.The FT-IR of the PEGDA/NIPAM polymer showed that the double bond peaks was weak.With the double bond was opened,the PEGDA/NIPAM copolymers had been synthesized.The contact angle of the polymers decreased,the equilibrium water content increased and the hydrophilicity enhanced with the increasing of NIPAM monomer.