木薯染料提取物的稳定性。早期的pH处理和储存温度

Sinta Anggraeni, N. Wartini, N. P. Suwariani
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引用次数: 0

摘要

木薯叶可以作为天然染料的来源。木薯叶含有相当高的叶绿素含量,可以提取成绿色染料提取物。本研究旨在确定木薯叶染料提取液在初始pH处理和储存温度下的稳定性,并确定为木薯叶染料提取液在储存过程中提供最佳稳定性的初始pH和温度。本实验采用双因素完全随机设计。第一个因素是初始pH值,它由pH 9、pH 10和pH 11组成。第二个因素是储存温度,包括低温(8±2℃)和室温(28±2℃)。对数据进行方差分析,以确定治疗对观察变量的影响。结果表明,贮藏过程中初始pH和温度处理及其相互作用影响了木薯叶色素提取物的总叶绿素含量、叶绿素a含量、叶绿素b含量、抗氧化能力、亮度值(L*)、红度值(a*)和黄度值(b*)。木薯叶染料提取液在初始pH为9、低温(8±2℃)条件下最稳定。木薯叶染料提取物贮藏7 d后,总叶绿素含量下降48.44%,叶绿素a下降46.86%,叶绿素b下降49.35%,抗氧化能力下降30.87%,红度值(a*)下降62.91%,但红度值(a*)、亮度值(L*)和黄度值(b*)分别比对照提高了62.91%、29.28%和49.02%。
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Stabilitas Ekstrak Pewarna Daun Singkong (Manihot esculenta C.) Pada Perlakuan pH Awal dan Suhu Penyimpanan
Cassava leaves are leaves that can be used as a source of natural dye. Cassava leaves have a fairly high chlorophyll content and can be extracted into green dye extract. This study aimed to determine how the stability of the cassava leaf dye extract at the initial pH treatment and storage temperature and to determine the initial pH and temperature that provide the best stability to the cassava leaf dye extract during storage. This experiment  used a completely randomized design with two factors. The first factor is the initial pH which consists of pH 9, pH 10 and pH 11. The second factor is the storage temperature consisting of cold temperature (8±2ºC) and room temperature (28±2ºC). The data were analyzed by analysis of variance to determine the effect of treatment on the observed variables. The results showed the initial pH and temperature treatment during storage and their interactions affected the total chlorophyll content, chlorophyll a content, chlorophyll b content, antioxidant capacity, brightness level value (L*), redness level value (a*) and yellowness level value ( b*) cassava leaf coloring extract. Cassava leaf dye extract was most stable at initial pH 9 and cold temperature (8±2ºC) during storage. Storage of cassava leaf dye extract for 7 days caused a decrease in total chlorophyll content of 48.44%, chlorophyll a by 46.86%, chlorophyll b by 49.35%, antioxidant capacity by 30.87%, redness level value (a*) by 62.91%, but caused an increase in the value of the redness level (a*) of 62.91%, the value of the brightness level (L*) of 29.28% and the value of the yellowness level (b*) of 49.02% against the control.
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