Scandola M, Ceccorulli G, Doi Y
Centro di Studio per la Fisica delle Macromolecole CNR, Universita di Bologna, Italy.
Int J Biol Macromol. 1990 Apr;12(2):112-7. doi: 10.1016/0141-8130(90)90062-f.
3-Hydroxybutyrate-3-hydroxyvalerate (3HB-3HV) as well as 3-hydroxybutyrate-4-hydroxybutyrate (3HB-4HB) copolyesters have been investigated by differential scanning calorimetry, thermogravimetric analysis and dynamic mechanical spectroscopy, over a wide range of compositions (0-95 mol% 3HV; 0-82 mol% 4HB). Both series of isolated copolyesters are partially crystalline at all compositions. Quenched samples show a glass transition that decreases linearly with increasing co-monomer molar fraction, more markedly when the co-monomer is 4HB. Above Tg, all copolyesters, rich in 3HB units, show a cold crystallization phenomenon followed by melting, while at the other end crystallization on heating is observed only in 3HB-3HV copolymers. The viscoelastic spectrum, strongly affected by thermal history, shows two relaxation regions: the glass transition, whose location depends on copolymer type and composition, and a secondary dispersion region at low temperatures (-130/-80 degrees C). The latter results from a water-related relaxation analogous to that of P(3HB) and, in 3HB-4HB copolymers, from another overlapping absorption peak centered at -130 degrees C, attributed to local motion of the methylene groups in the linear 4HB units.
通过差示扫描量热法、热重分析和动态力学光谱法,在广泛的组成范围内(3HV含量为0 - 95摩尔%;4HB含量为0 - 82摩尔%)对3 - 羟基丁酸 - 3 - 羟基戊酸(3HB - 3HV)以及3 - 羟基丁酸 - 4 - 羟基丁酸(3HB - 4HB)共聚酯进行了研究。两个系列的分离共聚酯在所有组成下均为部分结晶。淬火样品显示出玻璃化转变,其随着共聚单体摩尔分数的增加而线性降低,当共聚单体为4HB时更为明显。在玻璃化转变温度以上,所有富含3HB单元的共聚酯都呈现出冷结晶现象,随后是熔融,而在另一端,仅在3HB - 3HV共聚物中观察到加热时的结晶。受热历史强烈影响的粘弹性光谱显示出两个弛豫区域:玻璃化转变,其位置取决于共聚物类型和组成,以及在低温(-130 / -80℃)下的二级分散区域。后者源于与聚(3HB)类似的与水相关的弛豫,并且在3HB - 4HB共聚物中,源于另一个以-130℃为中心的重叠吸收峰,这归因于线性4HB单元中亚甲基的局部运动。