功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2012年
10期
1247-1250
,共4页
田晓飞%严永刚%李鸿%张刚%张其翼%吕国玉
田曉飛%嚴永剛%李鴻%張剛%張其翼%呂國玉
전효비%엄영강%리홍%장강%장기익%려국옥
氨基酸共聚物%合成%表征%降解%环保材料
氨基痠共聚物%閤成%錶徵%降解%環保材料
안기산공취물%합성%표정%강해%배보재료
poly(amino acid) (PAA)%preparation%characterization%degradation%eco-friendly materials
采用熔融缩聚法制备了一种新型可降解的6-氨基己酸(6N)和β-丙氨酸(βA)的二元共聚物(PAA),并研究了该共聚物的性能。采用红外光谱分析(FT-IR)、X射线衍射分析(XRD)、差示扫描量热分析(DSC)、热重分析(TGA)等手段对其结构进行了表征,结果表明,所合成的材料是2种单体的聚酰胺共聚物;随β-丙氨酸含量的增加,共聚物的结晶度、熔融温度呈先减小后增大的趋势,而分解温度呈依次减小的趋势,当共聚物中2种单体摩尔比为1∶1时,其为无定形共聚物。共聚物在去离子水中的降解实验结果表明,材料具有良好的降解性能;不同单体比例合成的共聚物中,共聚物的降解速率与共聚物的结晶度成反比,当聚合物中2种单体摩尔比为1∶1时,聚合物的降解速度最快,2周后几乎完全降解;整个降解过程中,降解液的pH值都维持在相对稳定的水平。在环保方面,该材料可望有良好的应用前景。
採用鎔融縮聚法製備瞭一種新型可降解的6-氨基己痠(6N)和β-丙氨痠(βA)的二元共聚物(PAA),併研究瞭該共聚物的性能。採用紅外光譜分析(FT-IR)、X射線衍射分析(XRD)、差示掃描量熱分析(DSC)、熱重分析(TGA)等手段對其結構進行瞭錶徵,結果錶明,所閤成的材料是2種單體的聚酰胺共聚物;隨β-丙氨痠含量的增加,共聚物的結晶度、鎔融溫度呈先減小後增大的趨勢,而分解溫度呈依次減小的趨勢,噹共聚物中2種單體摩爾比為1∶1時,其為無定形共聚物。共聚物在去離子水中的降解實驗結果錶明,材料具有良好的降解性能;不同單體比例閤成的共聚物中,共聚物的降解速率與共聚物的結晶度成反比,噹聚閤物中2種單體摩爾比為1∶1時,聚閤物的降解速度最快,2週後幾乎完全降解;整箇降解過程中,降解液的pH值都維持在相對穩定的水平。在環保方麵,該材料可望有良好的應用前景。
채용용융축취법제비료일충신형가강해적6-안기기산(6N)화β-병안산(βA)적이원공취물(PAA),병연구료해공취물적성능。채용홍외광보분석(FT-IR)、X사선연사분석(XRD)、차시소묘량열분석(DSC)、열중분석(TGA)등수단대기결구진행료표정,결과표명,소합성적재료시2충단체적취선알공취물;수β-병안산함량적증가,공취물적결정도、용융온도정선감소후증대적추세,이분해온도정의차감소적추세,당공취물중2충단체마이비위1∶1시,기위무정형공취물。공취물재거리자수중적강해실험결과표명,재료구유량호적강해성능;불동단체비례합성적공취물중,공취물적강해속솔여공취물적결정도성반비,당취합물중2충단체마이비위1∶1시,취합물적강해속도최쾌,2주후궤호완전강해;정개강해과정중,강해액적pH치도유지재상대은정적수평。재배보방면,해재료가망유량호적응용전경。
Amino acid polymers (PAA) based onβ-aminocaproic acid and β-alanine were prepared by melt con- densation polymerization and characterized by fourier transform infrared spectrometry (FT-IR), X-ray diffrac- tion (XRD) and differential scanning calorimetry (DSC). The results show that PAA is a kind of comonomers of polyamide polymers. The comonomers were amorphous polymers when the ratio of the two monomers was 1 : 1. The crystallization degree and melting point decrease first and then increase with β-alanine content of the comonomers increasing, while its decomposition temperature decreases gradually. The results of degradation of comonomers in water show that its degradation rate decreases first and then increases with β-alanine content of the comonomers increasing. The comonomers were degraded fastest and completely degraded in two weeks wile the monomer ratio is 1 : 1. The pH value of degradation liquid was relatively stable during the whole process. The comonomers would be potentially applied as eco-friendly materials.