NIRS determination of carbohydrates from hydrothermal-treated rice straw

TAPPI Journal ◽  
2012 ◽  
Vol 11 (4) ◽  
pp. 27-32 ◽  
Author(s):  
ANA MORAL ◽  
MARIA DOLORES HERNÁNDEZ ◽  
ANTONIO TIJERO ◽  
ZOILO GONZÁLEZ ◽  
JUAN GARCÍA ◽  
...  

Increasingly stringent environmental standards and the need for sustainable development are forcing pulp and paper mills to study methods to maximize the use of process wastes. Several studies have shown that “hydrothermal process” wastes might serve as raw material to obtain monosaccharides and oligosaccharides. High-performance liquid chromatography (HPLC) traditionally has been used to study these carbohydrates. However, HPLC has a series of disadvantages that could be avoided by use of other methods. This study evaluated the potential use of near infrared spectroscopy (NIRS) as a substitute analysis method for HPLC, using rice straw as raw material. The results showed that NIRS analysis can be used as a prediction method for monosaccharides and oligosaccharides. This method has the additional advantage of being a fast, nondestructive technique that does not require pretreatment of samples, and therefore, decreases the costs and the environmental impact of the analyses process.

Author(s):  
А.В. Вураско ◽  
Е.И. Симонова ◽  
А.Р. Минакова ◽  
Д.Д. Манойлович

Получение доступных сорбентов на основе природных материалов, для визуального колористического определения содержания ионов металлов в загрязненных природных и сточных водах является актуальным направлением исследований. Сорбенты на основе технической целлюлозы удовлетворяют этим требованиям. В работе для получения технической целлюлозы предложено использовать биомассу соломы риса. Для удаления из соломы риса минерального компонента при проведении окислительно-органосольвентной варки используют стадию щелочной обработки, которая приводит к деструкции полисахаридов, снижая выход технической целлюлозы. В связи с этим целью работы является изучение закономерностей проведения щелочной обработки соломы риса для максимального сохранения высокого выхода технической целлюлозы, извлечения минеральной части и возможности применения данной целлюлозы в качестве колористического сорбента. С учетом предварительных исследований найдены оптимальные значения технологических факторов, обеспечивающих высокий выход волокнистого материала из соломы риса при минимальном содержании в нем минеральных компонентов. Последующая органосольвентная варка позволяет получить техническую целлюлозу с выходом – 48,8% от абсолютно сухого сырья (а.с.с), зольностью 0,05% от а.с.с., содержанием лигнина 2,5% от а.с.с., удовлетворительными прочностными характеристиками, высокими сорбционными свойствами, необходимой белизной и рН водной вытяжки. Выявлено, что техническая целлюлоза из соломы риса содержит металлы, накопленные биомассой за вегетативный период. Щелочная обработка и окислительно-органосольвентная делигнификация в большинстве случаев приводят к снижению концентрации металлов в технической целлюлозе. Исключение составляют алюминий, железо и свинец, содержание которых в технической целлюлозе увеличивается. Таким образом, целлюлоза, полученная в оптимальных условиях щелочной обработки и последующей окислительно-органосольвентной варки из соломы риса, с учетом содержащихся в ней металлов, пригодна для использования в качестве сорбента для визуального колористического определения содержания ионов металлов в загрязненных природных и сточных водах. Receive available sorbents based on natural materials for visual color determination of the content of metal ions in contaminated natural and waste waters is a topical area of research. Sorbents on the basis of technical cellulose satisfy these requirements. In the process of obtaining technical cellulose is proposed to use biomass straw rice. Removal of straw rice mineral component when carrying out the oxidation-organosolvent use the cooking stage alkali treatment, which leads to degradation of polysaccharides, reducing the output of technical cellulose. In this regard, the aim of this work is to study the regularities of the alkaline treatment of rice straw for maximum preservation of the high output technical cellulose, extracting the mineral and the possibility of using the cellulose as the colour of the sorbent. Taking into account the preliminary studies, optimal conditions of technological factors were found ensuring a high yield of fibrous material from rice straw with a minimum content of mineral components in it. Subsequent organosolvent pulping yields technical pulp with a yield of 48.8% bone dry raw material (BDRM), an mineral ash content of 0.05% of BDRM, a lignin content of 2.5% of BDRM, satisfactory strength properties, high sorption properties, the necessary whiteness and pH of aqueous extract. It is revealed that the technical cellulose from straw of rice contains metals accumulated biomass during the vegetation period. Alkaline treatment and oxidative-organosolvent the delignification in most cases leads to a decrease of metal concentrations in pulp technical. With the exception of aluminum, iron and lead, the content of which is technical cellulose increases. Thus, cellulose obtained in optimum conditions of alkaline treatment and subsequent oxidation-organosolvent pulping of straw of rice, taking into account the contained metals suitable for use as a sorbent for visual color determination of the content of metal ions in polluted natural and sewage waters.


1998 ◽  
Vol 6 (A) ◽  
pp. A13-A19 ◽  
Author(s):  
T.G. Axon ◽  
R. Brown ◽  
S.V. Hammond ◽  
S.J. Maris ◽  
F. Ting

The early use of near infrared (NIR) spectroscopy in the pharmaceutical industry was for raw material identification, later moving on to some conventional “calibrations” for various ingredients in a variety of sample types. The approach throughout this development process has always been “conventional” with one measurement by NIR directly replacing some other slower method, be it Mid-IR identification, or determinations by Karl Fischer, high performance liquid chromatography (HPLC)etc. A significant change in approach was demonstrated by Plugge and Van der Vlies1 in 1993, where a qualitative system was used to provide “quantitative like” answers for potency of a drug substance. Following on from that key paper, there has been a realisation that the qualitative analysis ability of NIR, has the potential to be a powerful tool for process investigation, control and validation. The final step has been to develop “model free” approaches, that consider individual data sets as unique systems, and present the opportunity for NIR to escape the shackles of “calibration” in one form or another. The use of qualitative, or model free, approaches to NIR spectroscopy provides an effective tool for satisfying many of the demands of modern pharmaceutical production. “Straight through production,” “right first time,” “short cycle time” and “total quality management” philosophies can be realised. Eventually the prospect of parametric release may be materialised with a strong contribution from NIR spectroscopy. This paper will illustrate the above points with some real life examles.


2019 ◽  
Vol 13 (6) ◽  
pp. 1753-1766 ◽  
Author(s):  
Adam Schneider ◽  
Mark Flanner ◽  
Roger De Roo ◽  
Alden Adolph

Abstract. Broadband snow albedo can range from 0.3 to 0.9 depending on microphysical properties and light-absorbing particle (LAP) concentrations. Beyond the widely observed direct and visibly apparent effect of darkening snow, it is still unclear how LAPs influence snow albedo feedbacks. To investigate LAPs' indirect effect on snow albedo feedbacks, we developed and calibrated the Near-Infrared Emitting and Reflectance-Monitoring Dome (NERD) and monitored bidirectional reflectance factors (BRFs) hourly after depositing dust and black carbon (BC) particles onto experimental snow surfaces. After comparing snow infrared BRFs to snow specific surface areas (SSAs), we found that both measured and modeled snow infrared BRFs are correlated with snow SSA. These results, however, demonstrate a considerable uncertainty of ±10 m2 kg−1 in the determination of snow SSA from our BRF measurements. The nondestructive technique for snow SSA retrieval that we present here can be further developed for science applications that require rapid in situ snow SSA measurements. After adding large amounts of dust and BC to snow, we found more rapid decreasing of snow BRFs and SSAs in snow with added LAPs compared to natural (clean) snow but only during clear-sky conditions. These results suggest that deposition of LAPs onto snow can accelerate snow metamorphism via a net positive snow grain-size feedback.


2008 ◽  
Vol 91 (4) ◽  
pp. 739-743 ◽  
Author(s):  
Andréia de Haro Moreno ◽  
Hérida Regina Nunes Salgado

Abstract A rapid, accurate, and sensitive high-performance liquid chromatographic (HPLC) method was developed and validated for the determination of ceftazidime in pharmaceuticals. The method validation parameters yielded good results and included range, linearity, precision, accuracy, specificity, and recovery. The excipients in the commercial powder for injection did not interfere with the assay. Reversed-phase chromatography was used for the HPLC separation on a Waters C18 (WAT 054275; Milford, MA) column with methanolwater (70 + 30, v/v) as the mobile phase pumped isocratically at a flow rate of 1.0 mL/min. The effluent was monitored at 245 nm. The calibration graph for ceftazidime was linear from 50.0 to 300.0 g/mL. The values for interday and intraday precision (relative standard deviation) were <1. The results obtained by the HPLC method were calculated statistically by analysis of variance. We concluded that the HPLC method is satisfactory for the determination of ceftazidime in the raw material and pharmaceuticals.


Author(s):  
LAKSHMI NARASIMHA RAO KATAKAM ◽  
THIRUPATHI DONGALA

Objective: A novel study on a new liquid chromatographic approach has been developed and validated for simultaneous determination of trace level determination of sodium chloride and sodium sulfate measures its impurities using counter cation-exchange high-performance liquid chromatography with indirect ultraviolet (UV) detection. Methods: Chromatographic separation is developed and validated on a Hamilton PRP-X100 column with a mobile phase contained a mixture of the para-hydroxybenzoic acid buffer with a pH of 9.0 and methanol. Chromatography is developed at a flow rate of 2.0 mL/min with an indirect UV determination at 310 nm at a sensitivity level of 0.5%. The optimized method was validated as per the ICH Q2 guidelines. Results: The retention times of chloride and sulfate were about 2.8 and 7.6 min, respectively. The resolution between chloride and sulfate peaks is >4. Regression analysis confers a correlation coefficient for the stated compounds that are found to be >0.999. Conclusion: A novel analytical method was validated as per the ICH method validation guidelines and found to be selective. Hence, the validated analytical method was precise, specific, and accurate, and it is more economic and simple for the determination of inorganic impurities.


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