Noguchi Sarara, Kobayashi Takaomi
Department of Energy and Environment Engineering, Nagaoka University of Technology, 1603-1 Kamitomioka, Nagaoka 940-2188, Niigata, Japan.
Department of Science of Technology Innovation, Nagaoka University of Technology, 1603-1 Kamitomioka, Nagaoka 940-2188, Niigata, Japan.
Gels. 2022 Mar 9;8(3):172. doi: 10.3390/gels8030172.
A viscoelastic rheometer was equipped with a sono-device and a water bath to enable measurement of storage moduli G' and loss moduli G″ of biomass polysaccharide hydrogels such as Kanten agarose, -carrageenan, and konjac glucomannan under ultrasound (US) exposure. The action of low power of 43 kHz US on their hydrogels significantly decreased G' of Kanten agarose and carrageenan after a few seconds of US exposure 0.1% strain. When US with 20 W output power was exposed under mechanical strain at 0.1%, lower values were obtained cyclically for 3 min US intervals. The values then reverted to the original moduli values when US was stopped in cases of Kanten agarose and carrageenan hydrogels. As G″ values were increased during US operation, the anhydro-L-galactose segments in their hydrogels were unable to relax the external US forces within the gel sufficiently, thereby leading to gel structure collapse at a higher strain percentage. These results suggest that US exposure induced deformational change in the hydrogel structure formed by hydrogen-bonded cross-links. However, US deformation was less in the case of deacetylated cross-linkage in konjac glucomannan hydrogel.
一台粘弹性流变仪配备了超声装置和水浴,以便能够在超声(US)作用下测量生物质多糖水凝胶(如石花菜琼脂、κ-卡拉胶和魔芋葡甘露聚糖)的储能模量G'和损耗模量G″。在0.1%应变下,43kHz低功率超声作用于其水凝胶数秒后,石花菜琼脂和卡拉胶的G'显著降低。当20W输出功率的超声在0.1%机械应变下作用时,以3分钟超声间隔循环获得较低的值。在石花菜琼脂和卡拉胶水凝胶的情况下,当超声停止时,这些值随后恢复到原始模量值。由于在超声作用期间G″值增加,其水凝胶中的脱水-L-半乳糖片段无法充分松弛凝胶内的外部超声力,从而导致在较高应变百分比下凝胶结构崩溃。这些结果表明,超声作用诱导了由氢键交联形成的水凝胶结构的变形变化。然而,魔芋葡甘露聚糖水凝胶中脱乙酰化交联的情况下,超声变形较小。