On a molecular basis pelleting-induced changes on carbohydrate structure of co-products from bio-oil production revealed with vibrational molecular spectroscopy plus chemometrics: Sensitivity and response to conditioning temperature and time

IF 0.3 Q4 SPECTROSCOPY Biomedical Spectroscopy and Imaging Pub Date : 2017-01-05 DOI:10.3233/BSI-160153
Xuewei Huang, P. Yu
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Abstract

Molecular structure changes are closely related to nutrient utilization and availability. However, so far little research was found to determine the processing induced changes on carbohydrate structure in co-products from bio-oil processing. The objectives of this study were to investigate synergistic effects of conditioning temperature (70, 80 and 90°C) and time (50 and 75 s) during the pelleting process on carbohydrate structure profile of the co-products from bio-oil processing (canola meal). The vibrational molecular spectroscopy (ATR-VMS) with chemometrics was used to determine the impact of pelleting at different conditions on the inherent molecular structure changes. The molecular spectral analyses, Univariate and Multivariate spectral analyses, were used in this study. Multivariate spectral analyses included cluster analysis and principal analysis. The chemical functional groups mainly associated with carbohydrate structure profile in this lipid-free co-products (or with very little lipid) included cellulosic compounds (CEL, ranged at ca. 1302-1186 cm −1 ), structural CHO (SCHO, ranged at ca. 1488- 1186 cm −1 ) and total CHO (TCHO, ranged at ca. 1193-879 cm −1 ). The results showed that the pelleting process was able to alter inherent structures of CHO functional groups in the co-products from bio-oil processing. The univariate molecular analysis indicated that spectral intensities of CHO functional groups in the co-products were significantly affected by the pelleting process in the current study ( P< 0.05). Altering processing conditions resulted changes in molecular structure features of CHO functional groups except TCHO. The results of multivariate spectral analysis of CHO indicated that inherent CHO structural characteristics of all functional groups were not fully distinguished. This study demonstrated that the pelleting process under the conditions investigated caused partial changes in carbohydrate structures in terms of the spectral features of specific functional groups. These changes were not sufficient enough to make the entire spectral region of CHO functional groups become fully distinguishable. Future research is needed to investigate the interactive relationships between the absorption intensities of carbohydrate functional groups (TCHO, SCHO, CEL) and biodegradation and digestion of the co-products in order to reveal how carbohydrate molecular structure changes induced by processing affect nutritive availability.
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在分子基础上,振动分子光谱和化学计量学揭示了生物油生产副产物碳水化合物结构的变化:对调节温度和时间的敏感性和响应
分子结构的变化与养分的利用和有效性密切相关。然而,到目前为止,很少有研究确定加工引起的生物油加工副产物中碳水化合物结构的变化。本研究的目的是研究造粒过程中调节温度(70、80和90°C)和时间(50和75 s)对生物油加工副产物(油菜籽粕)碳水化合物结构特征的协同影响。采用化学计量的振动分子光谱(ATR-VMS)测定了不同条件下造粒对固有分子结构变化的影响。本研究采用分子光谱分析,单变量和多变量光谱分析。多元谱分析包括聚类分析和主成分分析。在这种无脂共产物中,主要与碳水化合物结构特征相关的化学官能团(或与很少的脂质相关)包括纤维素化合物(CEL,范围约1302-1186 cm−1)、结构CHO(SCHO,范围约1488-1186 cm−2)和总CHO(TCHO,范围约1193-879 cm−3)。结果表明,造粒工艺能够改变生物油加工副产物中CHO官能团的固有结构。单变量分子分析表明,在本研究中,共产物中CHO官能团的光谱强度受到造粒过程的显著影响(P<0.05)。改变加工条件会导致除TCHO外的CHO官能团分子结构特征发生变化。CHO的多变量谱分析结果表明,所有官能团固有的CHO结构特征没有完全区分。这项研究表明,在所研究的条件下,造粒过程导致碳水化合物结构在特定官能团的光谱特征方面发生部分变化。这些变化不足以使CHO官能团的整个光谱区域变得完全可区分。未来的研究需要研究碳水化合物官能团(TCHO、SCHO、CEL)的吸收强度与副产物的生物降解和消化之间的相互关系,以揭示加工引起的碳水化合物分子结构变化如何影响营养有效性。
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期刊介绍: Biomedical Spectroscopy and Imaging (BSI) is a multidisciplinary journal devoted to the timely publication of basic and applied research that uses spectroscopic and imaging techniques in different areas of life science including biology, biochemistry, biotechnology, bionanotechnology, environmental science, food science, pharmaceutical science, physiology and medicine. Scientists are encouraged to submit their work for publication in the form of original articles, brief communications, rapid communications, reviews and mini-reviews. Techniques covered include, but are not limited, to the following: • Vibrational Spectroscopy (Infrared, Raman, Teraherz) • Circular Dichroism Spectroscopy • Magnetic Resonance Spectroscopy (NMR, ESR) • UV-vis Spectroscopy • Mössbauer Spectroscopy • X-ray Spectroscopy (Absorption, Emission, Photoelectron, Fluorescence) • Neutron Spectroscopy • Mass Spectroscopy • Fluorescence Spectroscopy • X-ray and Neutron Scattering • Differential Scanning Calorimetry • Atomic Force Microscopy • Surface Plasmon Resonance • Magnetic Resonance Imaging • X-ray Imaging • Electron Imaging • Neutron Imaging • Raman Imaging • Infrared Imaging • Terahertz Imaging • Fluorescence Imaging • Near-infrared spectroscopy.
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