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Sample records for microcrystalline cellulose prepared

  1. Preparation and Characterization of Microcrystalline Cellulose (MCC from Kenaf and Cotton Stem

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    Farshad Mirehki

    2013-11-01

    Full Text Available Cellulose, microcrystalline cellulose (MCC and nanofiber cellulose are the ones of materials which are being used recently as biodegradable filler and reinforcing agent for making composites. In this research, microcrystalline cellulose were prepared from kenaf and cotton bast by hydrochloric acid hydrolysis. The effects of hydrolysis condition on amount of crystallinity and crystal size of MCC were investigated by infrared spectroscopy (FT-IR, X-ray diffraction (XRD and scanning electron microscopy (SEM. Results have shown that in both samples increasing the acid ratio increased the crystallinity; however, the size of crystals did not change. SEM results have shown that after hydrolysis the size of sample particles was micro.

  2. Crystallinity and thermal resistance of microcrystalline cellulose prepared from manau rattan (Calamusmanan)

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    Rizkiansyah, Raden Reza; Mardiyati, Steven, Suratman, R.

    2016-04-01

    The objective of this study was to prepare microcrystalline cellulose from Manau rattan (Calamusmanan) and to investigate the influence of concentration of sulfuric acid and hydrolysis time on crystallinity and thermal resistance of the microcrystalline cellulose (MCC). In this research, MCC was extracted through two stages, which is alkalization and acid hydrolysis. Alkalization was prepared by soaking manau rattan powder into sodium hydroxide (NaOH) 17.5wt% at 100°C for 8 hours. Acid hydrolysis was prepared by using sulfuric acid with concentration 0.1 M; 0.3 M; and 0.5 M for 4, 6, 8 and 10 hours. Crystallinity of MCC was measured by XRD, and thermal resistance was characterized by TGA. MCC was successfully extracted from manau rattan. The highest crystallinity of MCC obtained was 72.42% which prepared by acid hydrolysis with concentration 0.5 M for 10 hours. MCC prepared by acid hydrolysis with concentration 0.5 M for 10 hours not only resulted the highest crystallinity but also the best thermal resistance.

  3. Novel co-processed excipients of mannitol and microcrystalline cellulose for preparing fast dissolving tablets of glipizide

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    Jacob S

    2007-01-01

    Full Text Available Co-processed particles of microcrystalline cellulose and mannitol were fabricated by spray drying technique to be used as a direct compression excipient in fast dissolving tablet formulation. Microcrystalline cellulose passed through sieve no.80, having a volumetric mean diameter (d 50 of 28.35 µm, was used to form composite particles with powdered mannitol which was previously passed through sieve no. 80, in various mixing ratios. The composite particles were evaluated for their powder and compression properties. An increase in the microcrystalline cellulose proportion imparted greater compressibility to the composite particles, but the flowability of these mixtures was decreased. Although microcrystalline cellulose and mannitol have been extensively used in the formulation of fast dissolving tablets, the non-wetting property of the hard compact central core may delay the disintegration time. Optimized co-processed formulation containing mannitol and microcrystalline cellulose in the ratio of 1.25:1 was found to have optimized powder and compressibility characteristics with fast disintegrating property (< 15 s. Photomicrographs have shown that the mannitol crystals are fine and uniformly distributed in the microcrystalline matrix in spray dried form compared to physical mixture of the same combination. The fast disintegration may be due to the partial amorphization and formation of submicron particles of mannitol. These results indicated that improved fast dissolving tablets could be prepared by the co-processed mixture of microcrystalline cellulose and mannitol. Finally fast dissolving tablets of glipizide were prepared by blending with other excipients and compressed into tablets. Sensory study on disintegration time and mouth feel attributes ranked the present formulation based on grittiness, chalkiness and overall preference as the best.

  4. Preparation and Characterization of Cellulose Microcrystalline (MCC) from Fiber of Empty Fruit Bunch Palm Oil

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    Nasution, H.; Yurnaliza; Veronicha; Irmadani; Sitompul, S.

    2017-03-01

    Alpha cellulose which was isolated from cellulose of fiber empty fruit bunch palm oil was hidrolized with hydrochloric acid (2,5N) at 80°C to produce microcrystalline cellulose (MCC). Microcrystalline cellulose is an important additional ingredient in the pharmaceutical, food, cosmetics, and structural composites. In this study, MCC, alpha cellulose, and cellulose were characterized and thereafter were compared. Characterizations were made using some equipment such as x-ray diffraction (XRD), Fourier transform infrared (FTIR), scanning electron microscopy (SEM) and thermogravimetry analyzer (TGA). X-ray diffraction and infrared spectroscopy were studied to determine crystallinity and molecular structure of MCC, where scanning electron microscopy images were conducted for information about morfology of MCC. Meanwhile, thermal resistance of MCC was determined using thermogravimetry analyzer (TGA). From XRD and FTIR, the obtained results showed that the crystalline part was traced on MCC, where the –OH and C-O groups tended to reduced as alpha cellulose has changed to MCC. From SEM the image showed the reduction of particle size of MCC, while the thermal resistance of MCC was found lower as compared with cellulose and alpha cellulose as well, which was attributed to the lower molecular weight of MCC.

  5. 芦笋皮微晶纤维素的制备%Preparation of microcrystalline cellulose from asparagus peel

    Institute of Scientific and Technical Information of China (English)

    宋美玲

    2012-01-01

    以芦笋皮为原料,酶法制得膳食纤维后,采用盐酸水解,以溶胀性为指标确定制备微晶纤维素的工艺条件,为芦笋皮的加工利用提供一个新的途径。试验结果表明:在75℃下,盐酸浓度4 mol/L,料酸比1g∶5 mL,酸解时间5 h,制备出的微晶纤维素溶胀性可达6.90 mL/g,比芦笋皮中膳食纤维的溶胀性(4.80 mL/g)高2.10 mL/g。%Using asparagus as raw materials,microcrystalline cellulose was prepared in the best experimental conditions,determined by hydrochloric acid in different acidolysis time,acid concentration and proportion of material to acid,which took swelling as an index.And the best experimental conditions for preparation of microcrystalline cellulose provides a new way to process the asparagus.The results show that the best preparation conditions were the concentration of hydrochloric acid 4 mol/L,the proportion of material to acid 1∶5,acidolysis time 5 h,at 75 ℃.In the above conditions,the swelling of microcrystalline cellulose can be up to 6.90 mL/g,which is 2.10 mL/g more than the swelling(4.80 mL/g)of dietary fiber from the asparagus peel.

  6. Exploring the potential of polacrilin potassium as a novel superdisintegrant in microcrystalline cellulose based pellets prepared by extrusion-spheronization

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    Amita K Joshi

    2011-01-01

    Full Text Available Polacrilin potassium (PP, an ion exchange resin, was used as a superdisintegrant to improve the dissolution of rifampicin, from microcrystalline cellulose (MCC based pellets prepared by extrusion-spheronization. Production of fast release pellets by extrusion-spheronization using MCC is a complicated process. In the present study, pellets were prepared containing 50% w/w rifampicin (BCS class II drug and 40% w/w MCC as extrusion-spheronization aid. Different levels of PP and lactose ratio investigated were 0:10, 2:8, 4:6, 6:4, 8:2, and 10:0. Pellets were evaluated for yield, size, size distribution, shape, porosity, friability, residual moisture, and dissolution efficiency (DE at 30 minutes. Incorporation of this novel superdisintegrant had no adverse effect on the mechanical and micromeritic characteristics of pellets. All the batches of pellets showed high yields′, ~90%; narrow particle size distribution; aspect ratio, 1.0-1.1; friability, <1%; and porosity, 45.51-49.84%. Dissolution profiles were compared using model-independent approaches; DE and similarity factor, f 2 . Addition of Polacrilin results in significant improvement in the DE of rifampicin. The dissolution profiles were significantly different from the dissolution profile of pellets formulated without PP. This preliminary study indicates that PP can serve as an effective superdisintegrant in MCC pellets prepared by extrusion-spheronization.

  7. Preparation of nanocellulose from micro-crystalline cellulose: The effect on the performance and properties of agar-based composite films.

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    Shankar, Shiv; Rhim, Jong-Whan

    2016-01-01

    A facile approach has been performed to prepare nanocellulose (NC) from micro-crystalline cellulose (MCC) and test their effect on the performance properties of agar-based composite films. The NC was characterized by STEM, XRD, FTIR, and TGA. The NC was well dispersed in distilled water after sonication and their size was in the range of 100-500nm. The XRD results revealed the crystallinity of NC. The crystallinity index of NC (0.71) was decreased compared to the MCC (0.81). The effect of NC or MCC content (1, 3, 5 and 10wt% based on agar) on the mechanical, water vapor permeability (WVP), and thermal properties of the composites were studied. The NC obtained from MCC can be used as a reinforcing agent for the preparation of biodegradable composites films for their potential use in the development of biodegradable food packaging materials.

  8. Microcrystalline Cellulose from Plant Wastes through Sodium Hydroxide-Anthraquinone-Ethanol Pulping

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    Olugbenga Oludayo Oluwasina

    2014-08-01

    Full Text Available Microcrystalline cellulose was prepared from wastes of Tithonia diversifolia, inflorescence stems of Musa sapientum, and Musa paradisiaca by soda-anthraquinone–ethanol pulping method. They were bleached by sodium chlorite and then alpha-cellulose was isolated, followed by preparation of microcrystalline cellulose. The study revealed the effect of various processing stages on the properties of the cellulose obtained. Yields of more than 80% of microcrystalline cellulose were obtained. Fourier transform infrared (FTIR and solid state 13C Nuclear magnetic resonance (13C NMR confirmed the presence of the major expected peaks in microcrystalline cellulose. Scanning electron microscopy (SEM revealed that Musa species had short fiber length and mixtures of non-aggregated spherical, rod-shaped and thread like microcrystalline cellulose, but Tithonia diversifolia had aggregate crystal packed formation. The results compared well with those of other authors and were able to meet most of the requirements specified in British Pharmacopoeia. The study revealed that a drug excipient like microcrystalline cellulose that could protect thermo-labile active ingredients could be successfully obtained from abundant non-woody agricultural wastes.

  9. Fine granules showing sustained drug release prepared by high-shear melt granulation using triglycerin full behenate and milled microcrystalline cellulose.

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    Aoki, Hajime; Iwao, Yasunori; Uchimoto, Takeaki; Noguchi, Shuji; Kajihara, Ryusuke; Takahashi, Kana; Ishida, Masayuki; Terada, Yasuko; Suzuki, Yoshio; Itai, Shigeru

    2015-01-30

    This study aimed to prepare fine granules with a diameter less than 200μm and sustained drug release properties by melt granulation. Triglycerin full behenate (TR-FB) was examined as a new meltable binder (MB) by comparison of its properties with those of glycerin monostearate (GM), widely used as MB. The effect of milling microcrystalline cellulose (MCC), an excipient for melt granulation, on the granule properties was also investigated. TR-FB was more stable during heating and storage than GM, and produced smaller granules with narrower particle size distribution, larger yield in the 106-200μm range, uniform roundness and better sustained drug release profile than those prepared with GM. Granules prepared with milled MCC had almost the same physicochemical properties as those produced with intact MCC. However, milled MCC produced granules with a more rigid structure and smaller void space than intact MCC. Consequently, the granules produced with milled MCC showed better sustained drug release behavior than those prepared with intact MCC. We successfully prepared fine granules with sustained drug release properties and diameter of less than 200μm using TR-FB and milled MCC. Copyright © 2014 Elsevier B.V. All rights reserved.

  10. Physicotechnical, spectroscopic and thermogravimetric properties of powdered cellulose and microcrystalline cellulose derived from groundnut shells

    OpenAIRE

    Chukwuemeka P. Azubuike; Jimson O. Odulaja; Augustine O Okhamafe

    2012-01-01

    α-Cellulose and microcrystalline cellulose powders, derived from agricultural waste products, that have for thepharmaceutical industry, desirable physical (flow) properties were investigated. α–Cellulose (GCN) wasextracted from groundnut shell (an agricultural waste product) using a non-dissolving method based oninorganic reagents. Modification of this α -cellulose was carried out by partially hydrolysing it with 2Nhydrochloric acid under reflux to obtain microcrystalline cellulose (MCGN). Th...

  11. Visible light activated TiO2/microcrystalline cellulose nanocatalyst to destroy organic contaminants in water.

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    Hybrid TiO2/microcrystalline cellulose (MC) nanophotocatalyst was prepared in situ by a facile and simple synthesis utilizing benign precursors such as MC and TiCl4. The as-prepared nanocomposite was characterized by XRD, XPS, BET surface area analyzer, UV–vis DRS and TGA. Surfac...

  12. Visible light activated TiO2/microcrystalline cellulose nanocatalyst to destroy organic contaminants in water.

    Science.gov (United States)

    Hybrid TiO2/microcrystalline cellulose (MC) nanophotocatalyst was prepared in situ by a facile and simple synthesis utilizing benign precursors such as MC and TiCl4. The as-prepared nanocomposite was characterized by XRD, XPS, BET surface area analyzer, UV–vis DRS and TGA. Surfac...

  13. Structural changes in microcrystalline cellulose in subcritical water treatment.

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    Tolonen, Lasse K; Zuckerstätter, Gerhard; Penttilä, Paavo A; Milacher, Walter; Habicht, Wilhelm; Serimaa, Ritva; Kruse, Andrea; Sixta, Herbert

    2011-07-11

    Subcritical water is a high potential green chemical for the hydrolysis of cellulose. In this study microcrystalline cellulose was treated in subcritical water to study structural changes of the cellulose residues. The alterations in particle size and appearance were studied by scanning electron microscopy (SEM) and those in the degree of polymerization (DP) and molar mass distributions by gel permeation chromatography (GPC). Further, changes in crystallinity and crystallite dimensions were quantified by wide-angle X-ray scattering and (13)C solid-state NMR. The results showed that the crystallinity remained practically unchanged throughout the treatment, whereas the size of the remaining cellulose crystallites increased. Microcrystalline cellulose underwent significant depolymerization in subcritical water. However, depolymerization leveled off at a relatively high degree of polymerization. The molar mass distributions of the residues showed a bimodal form. We infer that cellulose gets dissolved in subcritical water only after extensive depolymerization.

  14. Compaction mechanism and tablet strength of unlubricated and lubricated (silicified) microcrystalline cellulose

    NARCIS (Netherlands)

    van Veen, B; Bolhuis, G K; Wu, Y S; Zuurman, K; Frijlink, H W

    This paper describes the differences in compaction properties between microcrystalline cellulose (MCC) and microcrystalline cellulose co-processed with colloidal silicon dioxide (SMCC). The different compaction parameters are not only compared for the pure materials, but also for the lubricated

  15. Comparison of microcrystalline characterization results from oil palm midrib alpha cellulose using different delignization method

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    Yuliasmi, S.; Pardede, T. R.; Nerdy; Syahputra, H.

    2017-03-01

    Oil palm midrib is one of the waste generated by palm plants containing 34.89% cellulose. Cellulose has the potential to produce microcrystalline cellulose can be used as an excipient in tablet formulations by direct compression. Microcrystalline cellulose is the result of a controlled hydrolysis of alpha cellulose, so the alpha cellulose extraction process of oil palm midrib greatly affect the quality of the resulting microcrystalline cellulose. The purpose of this study was to compare the microcrystalline cellulose produced from alpha cellulose extracted from oil palm midrib by two different methods. Fisrt delignization method uses sodium hydroxide. Second method uses a mixture of nitric acid and sodium nitrite, and continued with sodium hydroxide and sodium sulfite. Microcrystalline cellulose obtained by both method was characterized separately, including organoleptic test, color reagents test, dissolution test, pH test and determination of functional groups by FTIR. The results was compared with microcrystalline cellulose which has been available on the market. The characterization results showed that microcrystalline cellulose obtained by first method has the most similar characteristics to the microcrystalline cellulose available in the market.

  16. FTIR spectroscopy and X-ray powder diffraction characterization of microcrystalline cellulose obtained from alfa fibers

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    Trache D.

    2013-07-01

    Full Text Available Many cereal straws have been used as raw materials for the preparation of microcrystalline cellulose (MCC. These raw materials were gradually replaced with wood products; nevertheless about 10% of the world overall pulp production is obtained from non-wood raw material. The main interest in pulp made from straw is that it provides excellent fibres for different industries with special properties, and that it is the major available source of fibrous raw material in some geographical areas. The aim of the present work was to characterize microcrystalline cellulose prepared from alfa fibers using the hydrolysis process. The products obtained are characterized with FTIR spectroscopy and X-ray powder diffraction. As a result, FTIR spectroscopy is an appropriate technique for studying changes occurred by any chemical treatment. The spectrum of alfa grass stems shows the presence of lignin and hemicelluloses. However, the cellulose spectrum indicates that the extraction of lignin and hemicellulose was effective. The X-ray analysis indicates that the microcrystalline cellulose is more crystalline than the source material.

  17. Non-wood Fibre Production of Microcrystalline Cellulose from Sorghum caudatum: Characterisation and Tableting Properties

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    Ohwoavworhua, F. O.; Adelakun, T. A.

    2010-01-01

    The microcrystalline cellulose is an important ingredient in pharmaceutical, food, cosmetic and other industries. In this study, the microcrystalline cellulose, obtained from the stalk of Sorghum caudatum was evaluated for its physical and tableting characteristics with a view to assessing its usefulness in pharmaceutical tableting. The microcrystalline cellulose, obtained from the stalk of Sorghum caudatum, obtained by sodium hydroxide delignification followed by sodium hypochlorite bleachin...

  18. Characterization of Epoxy Composites Reinforced with Wax Encapsulated Microcrystalline Cellulose

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    Yuanfeng Pan

    2016-11-01

    Full Text Available The effect of paraffin wax encapsulated microcrystalline cellulose (EMC particles on the mechanical and physical properties of EMC/epoxy composites were investigated. It was demonstrated that the compatibility between cellulose and epoxy resin could be maintained due to partial encapsulation resulting in an improvement in epoxy composite mechanical properties. This work was unique because it was possible to improve the physical and mechanical properties of the EMC/epoxy composites while encapsulating the microcrystalline cellulose (MCC for a more homogeneous dispersion. The addition of EMC could increase the stiffness of epoxy composites, especially when the composites were wet. The 1% EMC loading with a 1:2 ratio of wax:MCC demonstrated the best reinforcement for both dry and wet properties. The decomposition temperature of epoxy was preserved up to a 5% EMC loading and for different wax:MCC ratios. An increase in wax encapsulated cellulose loading did increase water absorption but overall this absorption was still low (<1% for all composites.

  19. To prepare and characterize microcrystalline cellulose granules using water and isopropyl alcohol as granulating agents and determine its end-point by thermal and rheological tools.

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    Chaudhari, Smruti P; Dave, Rutesh H

    2015-05-01

    Microcrystalline cellulose (MCC-102) is one of the most commonly used excipient in the pharmaceutical industry. For this research purpose, authors have developed a different technique to determine the end point for MCC-102 using water and isopropyl alcohol 70% (IPA) as granulating agent. Wet and dry granules obtained were characterized for their flow properties using the powder rheometer and thermal analysis. Powder rheometer was used to measure basic flowability energy (BFE), specific energy (SE), percentage compressibility, permeability and aeration. Thermal analysis includes effusivity and differential scanning calorimetry (DSC) measurements. BFE and SE results showed water granules requires high energy as compared to IPA granules. Permeability and compressibility results suggest IPA forms more porous granules and have better compressibility as compared to water granules. Hardness data reveals interesting phenomena in which as the amount of water increases, hardness decreases and vice-versa for IPA. Optimal granules were obtained in the range of 45-55% w/w. DSC data supported the formation of optimal granules. Empirical measurements like angle of repose did not reveal any significant differences between powder flow among various granules. In this paper, with the help of thermal effusivity and powder rheology we were able to differentiate between various powder flows and determine the optimal range for granule formation.

  20. Facile synthesis of TiO2/microcrystalline cellulose nanocomposites: photocatalytically active material under visible light irradiation

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    Doped TiO2 nanocomposites were prepared in situ by a facile and simple synthesis utilizing benign and renewable precursors such as microcrystalline cellulose (MC) and TiCl4 through hydrolysis in alkaline medium without the addition of organic solvents. The as-prepared nanocompos...

  1. Facile synthesis of TiO2/microcrystalline cellulose nanocomposites: photocatalytically active material under visible light irradiation

    Science.gov (United States)

    Doped TiO2 nanocomposites were prepared in situ by a facile and simple synthesis utilizing benign and renewable precursors such as microcrystalline cellulose (MC) and TiCl4 through hydrolysis in alkaline medium without the addition of organic solvents. The as-prepared nanocompos...

  2. Compactibility of agglomerated mixtures of calcium carbonate and microcrystalline cellulose.

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    Garzón Serra, María de Lourdes; Villafuerte Robles, Leopoldo

    2003-06-04

    The tablet tensile strength (T) of agglomerated mixtures of microcrystalline cellulose-Avicel PH 102 (MC), calcium carbonate (CC) and polyvinylpyrrolidone (Povidone, PVP), lubricated with magnesium stearate (MS), and formed under a compaction pressure (P(c)) ranging up to 618MPa has been determined. The compactibility was defined through: ln(-ln(1-T/T(max)))=Slope x lnP(c)+Intercept. MC/CC mixtures added of an agglutinant, before and after lubrication, show an important positive effect on their tablet tensile strength compared to a lineal relationship. This positive effect becomes smaller with decreasing compaction pressures. By different mixing methods, the higher the mixing efficiency the higher the compactibility, following the order: spray-dried>wet massing>tumble mixing. The compactibility of MC/CC/PVP spray-dried mixtures with calcium carbonate content from 20 to 60% was equal to or greater than that of pure microcrystalline cellulose. After lubrication with 2% MS the compactibility decreased, only the mixture with the maximal tablet tensile strength attained the tensile strength of pure microcrystalline cellulose. The presence of the binder, the lubricant and higher compaction pressures allow the accommodation of higher calcium carbonate proportions in the mixtures, at the maximal tablet tensile strength of the series. The lubricant decreases in a greater extent the compactibility of mixtures with a continuous phase of MC/PVP than that of CC/PVP. This is attributed to the plastic behavior of the MC/PVP continuous phase compared to a calcium carbonate continuous phase able to disrupt the Povidone and the possible lubricant coatings allowing a stronger interparticle interaction.

  3. Application of ethyl cellulose, microcrystalline cellulose and octadecanol for wax based floating solid dispersion pellets.

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    Yan, Hong-Xiang; Zhang, Shuang-Shuang; He, Jian-Hua; Liu, Jian-Ping

    2016-09-01

    The present study aimed to develop and optimize the wax based floating sustained-release dispersion pellets for a weakly acidic hydrophilic drug protocatechuic acid to achieve prolonged gastric residence time and improved bioavailability. This low-density drug delivery system consisted of octadecanol/microcrystalline cellulose mixture matrix pellet cores prepared by extrusion-spheronization technique, coated with drug/ethyl cellulose 100cp solid dispersion using single-step fluid-bed coating method. The formulation-optimized pellets could maintain excellent floating state without lag time and sustain the drug release efficiently for 12h based on non-Fickian transport mechanism. Observed by SEM, the optimized pellet was the dispersion-layered spherical structure containing a compact inner core. DSC, XRD and FTIR analysis revealed drug was uniformly dispersed in the amorphous molecule form and had no significant physicochemical interactions with the polymer dispersion carrier. The stability study of the resultant pellets further proved the rationality and integrity of the developed formulation.

  4. Microcrystalline cellulose-carboxymethyl cellulose sodium as an effective dispersant for drug nanocrystals: A case study.

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    Dan, JiXiu; Ma, YueQin; Yue, PengFei; Xie, YuanBiao; Zheng, Qin; Hu, PengYi; Zhu, WeiFeng; Yang, Ming

    2016-01-20

    This study is aimed at seeking an alternative dispersant for spray drying of drug nanosuspensions. The ideal dispersant is not only able to prevent the agglomeration of drug nanocrystals in the suspension state, but also it is able to preserve redispersibility of drug nanocrystals after drying. An active pharmaceutical ingredient (API) was used as a model drug. API nanosuspensions were prepared by homogenization and converted into nanocrystals powder (API-NP) with microcrystalline cellulose-carboxymethyl cellulose sodium (MCCS) via spray drying. It was found that MCCS was able to prevent the aggregation of API-NP in the suspension state and the agglomeration during spray-drying process, possibility due to its high Zeta potential and steric barrier from network structure, and reduction of API size at nanoscale and incorporation into MCCS network structure did not affect the solid state of API as evidenced by DSC and XRD analysis. The spray-dried API-NP/MCCS powders exhibited excellent sphere-shape performance, and could easily redispersed to API-NC suspensions state. Dissolution of the spray-dried API-NP was distinctly superior to those of the crude powder and physical mixture, respectively. Within 30 min, approximate 85.87% of API was dissolved from the API-NP/MCCS. MCCS was demonstrated to be an effective dispersant for spray-dried drug nanocrystals and preservation of the nanocrystals associated with excellent redispersibility.

  5. Phloxine B as a Probe for Entrapment in Microcrystalline Cellulose

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    Enrique San Román

    2012-02-01

    Full Text Available The photophysical behaviour of phloxine B adsorbed onto microcrystalline cellulose was evaluated by reflectance spectroscopy and laser induced time-resolved luminescence in the picosecond-nanosecond and microsecond-millisecond ranges. Analysis of the absorption spectral changes with concentration points to a small tendency of the dye to aggregate in the range of concentrations under study. Prompt fluorescence, phosphorescence and delayed fluorescence spectral decays were measured at room temperature and 77 K, without the need of sample degassing because cellulose protects triplet states from oxygen quenching. In all cases, spectral changes with time and lifetime distribution analysis were consistent with the dye coexisting in two different environments: dyes tightly entrapped between polymer chains in crystalline regions of cellulose showed longer fluorescence and phosphorescence lifetimes and more energetic triplet states, while dyes adsorbed in more amorphous regions of the support showed shorter lifetimes and less energetic triplet states. This behaviour is discussed in terms of the different dye-support interactions in both kinds of adsorption sites.

  6. Dielectric barrier discharge plasma pretreatment on hydrolysis of microcrystalline cellulose

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    Fangmin, HUANG; Zhouyang, LONG; Sa, LIU; Zhenglong, Qin

    2017-04-01

    Dielectric barrier discharge (DBD) plasma was used as a pretreatment method for downstream hydrolysis of microcrystalline cellulose (MCC). The degree of polymerization (DP) of MCC decreased after it was pretreated by DBD plasma under a carrier gas of air/argon. The effectiveness of depolymerization was found to be influenced by the crystallinity of MCC when under the pretreatment of DBD plasma. With the addition of tert-butyl alcohol in the treated MCC water suspension solution, depolymerization effectiveness of MCC was inhibited. When MCC was pretreated by DBD plasma for 30 min, the total reducing sugar concentration (TRSC) and liquefaction yield (LY) of pretreated-MCC (PMCC) increased by 82.98% and 34.18% respectively compared with those for raw MCC.

  7. Dielectric barrier discharge plasma pretreatment on hydrolysis of microcrystalline cellulose

    Science.gov (United States)

    Huang, Fangmin; Long, Zhouyang; Liu, Sa; Qin, Zhenglong

    2017-04-01

    Dielectric barrier discharge (DBD) plasma was used as a pretreatment method for downstream hydrolysis of microcrystalline cellulose (MCC). The degree of polymerization (DP) of MCC decreased after it was pretreated by DBD plasma under a carrier gas of air/argon. The effectiveness of depolymerization was found to be influenced by the crystallinity of MCC when under the pretreatment of DBD plasma. With the addition of tert-butyl alcohol in the treated MCC water suspension solution, depolymerization effectiveness of MCC was inhibited. When MCC was pretreated by DBD plasma for 30 min, the total reducing sugar concentration (TRSC) and liquefaction yield (LY) of pretreated-MCC (PMCC) increased by 82.98% and 34.18% respectively compared with those for raw MCC.

  8. Silicone Rubber and Microcrystalline Cellulose Composites with Antimicrobial Properties

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    Virginija JANKAUSKAITĖ

    2014-04-01

    Full Text Available The goal of this study was to create polydimethylsiloxane (PDMS and microcrystalline cellulose (MCC composites with high mechanical properties and antimicrobial activity. Vinyl-terminated PDMS was mixed with bifunctional filler, which combines MCC stiffness and antimicrobial properties of silver nanoparticles. To provide antimicrobial properties the silver nanoparticles in situ were synthesized by chemical reducing method in MCC aqueous suspension. Silver nanoparticles (AgNPs concentration deposited on MCC particles surface was varied. The morphology, antimicrobial activity and mechanical properties of PDMS/MCC composites and their components have been investigated. It was shown that the combination of MCC/AgNPs as a filler and PDMS as matrix advantages bring multifunctional properties to polymer matrix composite. DOI: http://dx.doi.org/10.5755/j01.ms.20.1.4397

  9. Processing pharmaceutical grade microcrystalline cellulose from groundnut husk: Extraction methods and characterization

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    Ohwoavworhua Frank

    2009-01-01

    Full Text Available Microcrystalline cellulose (MCC is an important ingredient in pharmaceutical, food, cosmetic and other industries. In this work, MCC was prepared from the alpha cellulose content of groundnut husk, a renewable natural resource that has no industrial utilization yet. The effects of pulping methods (sodium hydroxide and multistage pulping and varying bleaching time on yield and amorphous properties of obtained alpha cellulose were examined. The prepared MCC (groundnut husk-MCC was characterized using scanning electron microscopy (SEM, infrared spectroscopy (FTIR, X-ray powder diffractometer (X-RPD, differential scanning calorimetry (DSC and compared with commercial-grade MCC. The results showed that complete pulping was achieved only by the use of the multistage pulping method and its yield was 15%. It was also found that the duration of bleaching affected the polymeric form of the processed alpha cellulose and hence, it is suggested that X-ray diffraction analysis should form an in-process check in the production of cellulose to ensure batch-to-batch consistency and performance. It was concluded that GH-MCC compared favourably with the commercial-grade MCC as well as conform to official specifications for MCC in the British Pharmacopoeia.

  10. Non-wood fibre production of microcrystalline cellulose from Sorghum caudatum: Characterisation and tableting properties

    OpenAIRE

    Ohwoavworhua F; Adelakun T

    2010-01-01

    The microcrystalline cellulose is an important ingredient in pharmaceutical, food, cosmetic and other industries. In this study, the microcrystalline cellulose, obtained from the stalk of Sorghum caudatum was evaluated for its physical and tableting characteristics with a view to assessing its usefulness in pharmaceutical tableting. The microcrystalline cellulose, obtained from the stalk of Sorghum caudatum, obtained by sodium hydroxide delignification followed by sodium hypochlorite bleachin...

  11. Compactibility of mixtures of calcium carbonate and microcrystalline cellulose.

    Science.gov (United States)

    Garzón, M de Lourdes; Villafuerte, Leopoldo

    2002-01-01

    A patented coprocessed mixture of microcrystalline cellulose (MC) and calcium carbonate (CC) is claimed to perform, as a pharmaceutical excipient, equal or better than pure MC. To investigate it, the tensile strength (T) of tablets made of mixtures of MC type 102, CC, magnesium stearate (MS) and polyvinylpyrrolidone (PVP) and formed under a compaction pressure (P(c)) ranging up to 618 MPa has been determined. The compactibility of the mixtures was defined through regression parameters obtained with ln(-ln(1-T/T(max)))=slope x lnP(c) + intercept. MC/CC mixtures, P(c)=618 MPa, show a small decrease in tablet tensile strength with CC proportions up to about 20%, falling considerably thereafter. Lower compaction pressures, P(c)tablet tensile strength due to 2%-MS, P(c)=487 MPa, was recovered to 35% of its original value admixing about 25% CC. This maximal value of recovery showed a shift to lower proportions of CC, up to 10%, as compaction pressure decreased. This was attributed to lower CC-particles fragmentation or agglomerates spreading at lower compaction pressures. Mixtures with increased plasticity (MC/CC/PVP and MC/CC/PVP/MS) showed an increased compactibility, which was more evident at higher compaction pressures and higher CC proportions, presumably due to higher deformation and erosion of PVP particles. Inclusion of about 40% CC in a MC/PVP/MS mixture showed 60% recovery of the original MC tablet tensile strength. Lower MS proportions are expected to allow a higher recovery.

  12. Physicochemical properties and characteristics of microcrystalline cellulose derived from the cellulose of oil palm empty fruit bunch

    Science.gov (United States)

    Nasution, H.; Yurnaliza; Veronicha; Irmadani; Sitompul, S.

    2017-07-01

    Cellulose from oil palm empty fruit bunch was hydrolyzed with different concentration of hydrochloric acid (HCl) viz. 2; 2.5; 3; 3.5 N to prepare microcrystalline cellulose (MCC). The temperature of hydrolysis process was at 75 °C. The physicochemical properties such as organoleptic characteristic, water soluble substance, and loss on drying were conducted during this study. Infrared, x-ray diffraction, and scanning electron microscope (SEM) image were also performed to investigate the effect of hydrolysis on the molecular structure, crystal structure and morphology of the MCC, respectively. The results have showed, in term of the physicochemical properties, for all concentrations of HCl the MCC was obtained. The FTIR results showed the -OH functional group tended to reduced as alpha cellulose has changed to MCC. The x-ray diffraction pattern revealed that the crystal structure was traced on MCC where the highest was observed at hydrolysis process of 2.5N HCl. The image from SEM displayed an individualized and fibrous MCC on the treatment of 2.5N HCl.

  13. Influence of Tableting on Enzymatic Activity of Papain along with Determination of Its Percolation Threshold with Microcrystalline Cellulose.

    Science.gov (United States)

    Sharma, Manu; Sharma, Vinay; Majumdar, Dipak K

    2014-01-01

    The binary mixture tablets of papain and microcrystalline cellulose (MCC), dicalcium phosphate dihydrate (DCP), carrageenan, tragacanth, and agar were prepared by direct compression. Carrageenan, tragacanth, and agar provided maximum protection to enzyme activity compared to MCC and DCP. However, stability studies indicated highest loss of enzyme activity with carrageenan, tragacanth, and agar. Therefore, compression behaviour of different binary mixtures of papain with MCC at different compaction pressures, that is, 40-280 MPa, was studied according to Heckel equation. The compressibility studies of binary mixtures indicated brittle behavior of papain. The application of percolation theory on the relationship between critical density as a function of enzyme activity and mixture composition revealed the presence of percolation threshold for binary mixture. Papain-MCC mixture composition showed significant percolation threshold at 18.48% (w/w) papain loading. Microcrystalline cellulose provided higher protection during stability study. However, higher concentrations of microcrystalline cellulose, probably as dominant particles, do not protect the enzyme with their plastic deformation. Below the percolation threshold, that is, 18.48% (w/w) papain amount in mixture with plastic excipient, activity loss increases strongly because of higher shearing forces during compaction due to system dominance of plastic particles. This mixture range should therefore be avoided to get robust formulation of papain.

  14. Extraction of microcrystalline cellulose from rice straw and its effect on polyvinyl alcohol biocomposites film

    Science.gov (United States)

    Chin, Kwok-Mern; Ting, Sam Sung; Lin, Ong Hui; Owi, Wei Tieng

    2017-07-01

    The poor management and underutilization of agricultural wastes had proliferated interest of researchers around the world to find alternatives to utilize them as potential value-added products. One of the green alternatives is by extracting cellulose from these waste materials and incorporating them in polymer as reinforcement fillers. The surging amount of plastic waste also posed major issues to the environment due to its recalcitrance to degrade. Microcrystalline cellulose (MCC-RS) was extracted from rice straw through cyclic alkaline and bleaching treatment to remove hemicellulose and lignin respectively. Polyvinyl alcohol (PVOH) was chosen as the matrix and different ratios of PVOH / MCC-RS films were prepared (2.5, 5.0, 7.5 and 10.0wt% of MCC) through solution casting method and its tensile, thermal and morphological properties were studied. X-ray powder diffraction (XRD) results showed increased crystallinity of MCC-RS after chemical treatment (from 44.5% to 60.8%) due to the successful removal of lignin and hemicellulose, which was then confirmed with Fourier transform infrared spectroscopy (FTIR) results. For the biocomposites, both tensile strength and Young's modulus of the films increased with increasing MCC-RS content up until 7.5wt%, supported with scanning electron microscopy (SEM) results which depicted improvement in the interfacial adhesion between MCC-RS and PVOH. From the overall results, the improvement in properties of biocomposite from cellulose-based microfiller had shown promising future in application of the water soluble plastic packaging industry.

  15. Optimisation of the composition and production of mannitol/microcrystalline cellulose tablets

    NARCIS (Netherlands)

    Westerhuis, J.A; de Haan, P; Zwinkels, J; Jansen, W.T; Coenegracht, P.M J; Lerk, C.F

    1996-01-01

    Mixtures of mannitol and microcrystalline cellulose (MCC) were investigated on a small-production scale by granulation in a high-shear mixer and compression into tablets. For both excipients only a few cases of incompatibilities with active ingredients are known. Tablets with only MCC as the filler

  16. The rheological properties of modified microcrystalline cellulose containing high levels of model drugs.

    Science.gov (United States)

    Knight, Paul E; Podczeck, Fridrun; Newton, J Michael

    2009-06-01

    The rheological properties of different types of microcrystalline cellulose (MCC) mixed with model drugs and water have been evaluated to identify the influence of sodium carboxymethylcellulose (SCMC) added to the cellulose during preparation. A ram extruder was used as a capillary rheometer. The mixtures consisted of 20% spheronizing agent (standard grade MCC or modified types with 6% or 8% of low viscosity grade SCMC) and 80% of ascorbic acid, ibuprofen or lactose monohydrate. The introduction of SCMC changed all rheological parameters assessed. It produced more rigid systems, requiring more stress to induce and maintain flow. Degree of non-Newtonian flow, angle of convergence, extensional viscosity, yield and die land shear stress at zero velocity, and static wall friction were increased, but recoverable shear and compliance were decreased. The presence of SCMC did not remove the influence of the type of drug. The mixture of ibuprofen and standard MCC had the lowest values for shear stress as a function of the rate of shear, extensional viscosity, and angle of convergence, but the highest values for recoverable shear and compliance. The findings indicate that the system has insufficient rigidity to form pellets.

  17. 微晶纤维素的研究进展%Research progress of microcrystalline cellulose

    Institute of Scientific and Technical Information of China (English)

    吴伟兵; 庄志良; 景宜; 戴红旗

    2013-01-01

    Microcrystalline cellulose (MCC) is an important research area in material and polymer science because of their particular size and structure,and the abundant,renewable,biodegradable and biocompatible cellulose matrix.Acid hydrolysis and enzymatic hydrolysis are the main methods for preparing MCC.Besides the wide applications in traditional industries,MCC has important applications in the areas of reinforced composite,biomedicine,photoelectric science,etc.Finally,the future development of MCC is prospected.%微晶纤维素具有独特的尺寸结构,其基质纤维素丰富价廉、可再生降解并具有良好的生物相容性,是天然高分子材料的重要分支.微晶纤维素的制备方法主要有酸水解法和酶解法;微晶纤维素除在传统行业有广泛应用外,还在增强复合、生物医学和光电科学等新兴领域有重要应用.最后对微晶纤维素的未来发展进行了展望和期待.

  18. Influence of Water on the Structure and Dielectric Properties of the Microcrystalline and Nano-Cellulose

    Science.gov (United States)

    Kovalov, Kostiantyn M.; Alekseev, Olexander M.; Lazarenko, Maxim M.; Zabashta, Yu F.; Grabovskii, Yurii E.; Tkachov, Sergii Yu

    2017-07-01

    Influence of water in the different states on a structure and dielectric properties of microcrystalline cellulose were studied by of X-ray, thermogravimetry, and dielectric spectroscopy. At research of microcrystalline cellulose (MCC) with different content of water, it is shown that the molecules of water are located in the macropores of MCC and in multimolecular hydrated layers. It is shown that at the increase of concentration of water in a hydrated shell, the reorganization of molecules of cellulose in the surface of crystallites takes place, and as a result, their transversal size and crystallinity increase. It is shown that during the concentration of water, more than 13% in a continuous hydrated shell of crystallites appears. Temperature dependences of actual and imaginary parts of complex dielectric permittivity were studied in the interval of temperatures [-180 ÷ 120] °C on frequencies of f = 5, 10, 20, and 50 kHz. A low-temperature relaxation process and high-temperature transition were observed. Low-temperature relaxation process which is related to transition of surface methylol groups of molecules of cellulose conformation from tg to tt is shifted toward low temperatures at the increase of concentration of water in microcrystalline cellulose.

  19. Microwave assisted conversion of microcrystalline cellulose into value added chemicals using dilute acid catalyst.

    Science.gov (United States)

    Ching, Teck Wei; Haritos, Victoria; Tanksale, Akshat

    2017-02-10

    One of the grand challenges of this century is to transition fuels and chemicals production derived from fossil feedstocks to renewable feedstocks such as cellulosic biomass. Here we describe fast microwave conversion of microcrystalline cellulose (MCC) in water, with dilute acid catalyst to produce valuable platform chemicals. Single 10min microwave assisted treatment was able to convert >60% of MCC, with >50mol% yield of desirable products such as glucose, HMF, furfural and levulinic acid. Recycling of residual MCC with make-up fresh MCC resulted in an overall conversion of >93% after 5 cycles while maintaining >60% conversion in each cycle. Addition of isopropanol (70%v/v) as a co-solvent increased the yields of HMF and levulinic acid. This work shows for the first time proof of concept for complete conversion of recalcitrant microcrystalline cellulose in mild conditions of low temperature, dilute acid and short residence time using energy efficient microwave technology.

  20. Preparation of microcrystalline single junction and amorphous-microcrystalline tandem silicon solar cells entirely by hot-wire CVD

    Energy Technology Data Exchange (ETDEWEB)

    Kupich, M.; Grunsky, D.; Kumar, P.; Schroeder, B. [University of Kaiserslautern (Germany). Department of Physics

    2004-01-25

    The hot-wire chemical vapour deposition (HWCVD) has been used to prepare highly conducting p- and n-doped microcrystalline silicon thin layers as well as highly photoconducting, low defect density intrinsic microcrystalline silicon films. These films were incorporated in all-HWCVD, all-microcrystalline nip and pin solar cells, achieving conversion efficiencies of {eta}=5.4% and 4.5%, respectively. At present, only the nip-structures are found to be stable against light-induced degradation. Furthermore, microcrystalline nip and pin structures have been successfully incorporated as bottom cells in all-hot-wire amorphous-microcrystalline nipnip- and pinpin-tandem solar cells for the first time. So far, the highest conversion efficiencies of the 'micromorph' tandem structures are {eta}=5.7% for pinpin-solar cells and 7.0% for nipnip solar cells. (author)

  1. Green synthesis of hybrid graphene oxide/microcrystalline cellulose aerogels and their use as superabsorbents

    Energy Technology Data Exchange (ETDEWEB)

    Wei, Xiao; Huang, Ting; Yang, Jing-hui; Zhang, Nan; Wang, Yong, E-mail: yongwang1976@163.com; Zhou, Zuo-wan

    2017-08-05

    Highlights: • Hybrid GO/MCC aerogels were prepared using LiBr aqueous solution as the solvent. • GO was exfoliated by MCC through the strong interaction between them. • The adsorption ability of GO per unit mass in the hybrid aerogels was greatly enhanced. - Abstract: In this work, we developed a green synthesis method to prepare the hybrid aerogels containing graphene oxide (GO) and microcrystalline cellulose (MCC) using lithium bromide (LiBr) aqueous solution as the solvent, which insured the complete dissolution of MCC. The interaction between GO and MCC was investigated through different methods The results demonstrate that there is a strong interaction between GO and MCC molecules, which promotes the exfoliation of GO in the hybrid aerogels. The hybrid GO/MCC aerogels exhibit typical three dimensional porous structure and the pore morphology can be well adjusted by changing the content of GO. The adsorption ability of the hybrid aerogels was measured using methylene blue (MB) as an adsorbate. The results show that the adsorption ability of GO per unit mass is greatly enhanced compared with the pure GO aerogel, especially at relatively low GO content the adsorption amount of GO per unit mass is enhanced up to 2630 mg/g. Further results demonstrate that the hybrid GO/MCC aerogels still obey the pseudo-second-order adsorption model, which is similar to that of the pure GO aerogel. The mechanism for the amplified adsorption ability of GO in the hybrid GO/MCC aerogels is then analyzed.

  2. Supramolecular elucidation of the quality attributes of microcrystalline cellulose and isomalt composite pellet cores.

    Science.gov (United States)

    Antal, István; Kállai, Nikolett; Luhn, Oliver; Bernard, Jörg; Nagy, Zsombor Kristóf; Szabó, Barnabás; Klebovich, Imre; Zelkó, Romána

    2013-10-01

    The major objective of this study was to disclose the relationships between the physical quality attributes and supramolecular structure of novel composite pellet cores containing microcrystalline cellulose (MCC) and isomalt in different ratios. The novel composite pellet cores were manufactured by an extrusion/spheronisation process. The micro or supramolecular structure of pellets was tracked by positron annihilation lifetime spectroscopy (PALS) based on the o-Ps lifetime values. The results indicate a correlation between the examined macro and microstructural properties of the inert cores. The higher free volume holes indicated by the higher o-Ps lifetime values resulted in a more mobile micro- and supramolecular structure of MCC cores thus increasing the plastic deformation and the tensile strength of the cores. A physical interaction was found between the microcrystalline cellulose and isomalt which supports the osmotic effect of the water soluble sugar alcohol in the composite pellet cores regarding drug release.

  3. Evaluation of Drug Release From Coated Pellets Based on Isomalt, Sugar, and Microcrystalline Cellulose Inert Cores

    OpenAIRE

    2010-01-01

    The objective of the present study was to investigate the effect of the pellet core materials isomalt, sugar, and microcrystalline cellulose on the in vitro drug release kinetics of coated sustained-release pellets as well as to evaluate the influence of different ratios of polymethacrylate copolymers exhibiting different permeability characteristics on the drug release rate. For characterization of the drug release process of pellets, the effect of osmolality was studied using glucose as an ...

  4. Densification-induced conductivity percolation in high-porosity pharmaceutical microcrystalline cellulose compacts

    Science.gov (United States)

    Strømme, M.; Niklasson, G. A.; Ek, R.

    2003-01-01

    The percolation theory is established as a useful tool in the field of pharmaceutical materials science. It is shown that percolation theory, developed for analyzing insulator-conductor transitions, can be applied to describe imperfect dc conduction in pharmaceutical microcrystalline cellulose during densification. The system, in fact, exactly reproduces the values of the percolation threshold and exponent estimated for a three-dimensional random continuum. Our data clearly show a crossover from a power-law percolation theory region to a linear effective medium theory region at a cellulose porosity of ˜0.7.

  5. The effect of wax on compaction of microcrystalline cellulose beads made by extrusion and spheronization.

    Science.gov (United States)

    Iloañusi, N O; Schwartz, J B

    1998-01-01

    The effect of wax on the deformation behavior and compression characteristics of microcrystalline cellulose (Avicel PH-101) and acetaminophen (APAP) beads is described. Beads of Avicel PH-101 and APAP formulations were prepared using extrusion and spheronization technology. A waxy material, glyceryl behenate, N.F. (Compritol), was added to the formulations in amounts ranging from 10% to 70% of total solid weight. Beads with a selected particle size range of 16-30 mesh were compressed with an instrumented single punch Manesty F press utilizing a 7/16-in. flat-faced tooling set. Compaction profiles were generated for the tablets to evaluate the effect of wax on the densification of beads containing wax. Beads made without wax (the control formulation) required greater compression forces to form cohesive tablets. As the amount of wax in the bead formulation was increased, the beads become more plastic and compressible. The Heckel equation which relates densification to compression pressure was used to evaluate the deformation mechanisms of the bead formulations. The analysis shows that as the level of wax in the bead formulation is increased, the yield pressure decreases, indicating that the beads densify by a plastic deformation mechanism.

  6. Formulation of ranitidine pellets by extrusion-spheronization with little or no microcrystalline cellulose.

    Science.gov (United States)

    Basit, A W; Newton, J M; Lacey, L F

    1999-01-01

    The present study was concerned with the feasibility of formulating ranitidine into pellets with a range of alternative excipients in place of microcrystalline cellulose (MCC). Eight ranitidine formulations employing two or more of the excipients lactose, barium sulfate, glyceryl monostearate, and MCC were processed by extrusion-spheronization, and characterized according to a series of physico-mechanical and dissolution criteria. Formulations containing lactose produced unsatisfactory pellets of wide size distribution and irregular shape, whereas formulations incorporating barium sulfate and glyceryl monostearate with or without MCC resulted in relatively spherical pellets of narrow size distribution and good mechanical properties. Ranitidine release was found to be rapid and virtually complete within 15 min, regardless of the pellet formulation. A direct relationship was observed between the concentration of MCC in the formulation and the properties of the pellets. In general, the higher the concentration of MCC, the rounder, stronger, and less friable the pellets. However, even pellets without MCC were also successfully prepared with a superior size distribution and shape over those with MCC. Overall, these results confirm that ranitidine can be formulated into pellet dosage forms with little or no MCC by the extrusion-spheronization process.

  7. Melt-processed poly(vinyl alcohol) composites filled with microcrystalline cellulose from waste cotton fabrics.

    Science.gov (United States)

    Sun, Xunwen; Lu, Canhui; Liu, Yong; Zhang, Wei; Zhang, Xinxing

    2014-01-30

    Waste cotton fabrics (WCFs), which are generated in a large volume from the textile industry, have caused serious disposal problem. Recycling WCFs into value-added products is one of the vital measures for both environmental and economic benefits. In this study, microcrystalline cellulose (MCC) was prepared by acid hydrolysis of WCFs, and used as reinforcement for melt-processed poly(vinyl alcohol) (PVA) with water and formamide as plasticizer. The microstructure and mechanical properties of the melt-processed PVA/MCC composites were characterized by Fourier transform infrared spectra, Raman spectra, differential scanning calorimetry, thermal gravimetric analysis, X-ray diffraction, tensile tests and dynamic mechanical analysis. The results indicated that MCC could establish strong interfacial interaction with PVA through hydrogen bonding. As a result, the crystallization of PVA was confined and its melting temperature was decreased, which was beneficial for the melt-processing of PVA. Compared with the unfilled PVA, the PVA/MCC composites exhibited remarkable improvement in modulus and tensile strength.

  8. A novel process for synthesis of spherical nanocellulose by controlled hydrolysis of microcrystalline cellulose using anaerobic microbial consortium.

    Science.gov (United States)

    Satyamurthy, P; Vigneshwaran, N

    2013-01-10

    Degradation of cellulose by anaerobic microbial consortium is brought about either by an exocellular process or by secretion of extracellular enzymes. In this work, a novel route for synthesis of nanocellulose is described where in an anaerobic microbial consortium enriched for cellulase producers is used for hydrolysis. Microcrystalline cellulose derived from cotton fibers was subjected to controlled hydrolysis by the anaerobic microbial consortium and the resultant nanocellulose was purified by differential centrifugation technique. The nanocellulose had a bimodal size distribution (43±13 and 119±9 nm) as revealed by atomic force microscopy. A maximum nanocellulose yield of 12.3% was achieved in a span of 7 days. While the conventional process of nanocellulose preparation using 63.5% (w/w) sulfuric acid resulted in the formation of whisker shaped nanocellulose with surface modified by sulfation, controlled hydrolysis by anaerobic microbial consortium yielded spherical nanocellulose also referred to as nano crystalline cellulose (NCC) without any surface modification as evidenced from Fourier transform infrared spectroscopy. Also, it scores over chemo-mechanical production of nanofibrillated cellulose by consuming less energy due to enzyme (cellulase) assisted catalysis. This implies the scope for use of microbial prepared nanocellulose in drug delivery and bio-medical applications requiring bio-compatibility. Copyright © 2012 Elsevier Inc. All rights reserved.

  9. EPR response of sucrose and microcrystalline cellulose to measure high doses of gamma radiation; Respuesta EPR de sacarosa y celulosa micro cristalina para medir altas dosis de radiacion gamma

    Energy Technology Data Exchange (ETDEWEB)

    Torijano, E.; Cruz, L.; Gutierrez, G.; Azorin, J.; Aguirre, F. [Universidad Autonoma Metropolitana, Unidad Iztapalapa, Av. San Rafael Atlixco 186, Col. Vicentina, 09340 Mexico D. F. (Mexico); Cruz Z, E., E-mail: eftc@xanum.uam.mx [UNAM, Instituto de Ciencias Nucleares, Circuito Exterior, Ciudad Universitaria, 04510 Mexico D. F. (Mexico)

    2015-10-15

    Solid dosimeters of sucrose and microcrystalline cellulose (Avicel Ph-102) were prepared, following the same process, in order to compare their EPR response against that of the l-alanine dosimeters considered as reference. All lots of dosimeters were irradiated with gamma radiation in Gamma beam irradiator with 8 kGy/h of the Nuclear Sciences Institute of UNAM. Doses ranged from 1 to 10 kGy respectively. We found that both the response of sucrose as microcrystalline cellulose were linear; however, the response intensity was, on average, twenty times more for sucrose. Comparing this against the EPR response of l-alanine in the range of doses, it was found that the response to sucrose is a third part; and microcrystalline cellulose is a sixtieth, approximately. The results agree with those found in the literature for sucrose, leaving open the possibility of investigating other dosage ranges for cellulose. (Author)

  10. FRACTIONATION OF HYDROLYZED MICROCRYSTALLINE CELLULOSE BY ULTRAFILTRATION MEMBRANE

    Directory of Open Access Journals (Sweden)

    NGUYEN HUYNH THAO THY

    2016-01-01

    Full Text Available Bioethanol process using cellulosic materials have been emerging an interesting field with a high potential of replacing petroleum-based fuel, as a future alternative. This work emphasised on improvement of enzymatic hydrolysis of alkaline NaOH-pretreated cellulose by applying an ultrafiltration membrane 10 kDa cutoff in order to minimise sugar inhibition on enzymes, reuse enzyme in hydrolysis and recover sugar for the subsequent fermentation. An improvement in the methodology of the enzymatic hydrolysis with ultrafiltration was made that the membrane was installed at the end of a tube connecting with a peristaltic pump to continuously remove glucose from hydrolysis reaction hence sugar was unable to inhibit enzyme activity and enzyme was retained inside the reactor for the reusing purpose. The combination of NaOH 1M alkaline pretreatment, enzymatic hydrolysis of cellulose with the optimum 3% enzyme dosage, ultrafiltration 10 kDa cutoff was evaluated to obtain the highest sugar concentration at 9 mg/ml after 6 hour hydrolysis. In comparison between hydrolysis with ultrafiltration and hydrolysis without ultrafiltration, the sugar concentration in hydrolysis with ultrafiltration was very much higher than that in hydrolysis without ultrafiltration in all enzyme dosages (1.5%, 3%, 6%. The hydrolysis with filtration produced a time profile in six hours with continuously significant increase in the sugar concentration. Only a small reduction initially for 1.5% dosage and no reduction in sugar concentration in 3% and 6% dosages. Hence the effect of product inhibition in hydrolysis was minimised as a result. In addition, a direct relationship between sugar concentration inside hydrolysis reactor, enzyme dosage and rate of sugar removal was observed during the hydrolysis process. Higher enzyme dosage in hydrolysis required a higher rate of sugar removal sufficiently to avoid inhibition in hydrolysis reaction.

  11. Preparation of 5-HMF directly from microcrystalline cellulose in ionic liquid system%在离子液体体系中由微晶纤维素直接制得5-羟甲基糠醛

    Institute of Scientific and Technical Information of China (English)

    杨伟伟; 王少君

    2012-01-01

    Process of microcrystalline cellulose(MC) dehydration to 5-hydroxymethyl-furaldehyde(5-HMF) using [Bmim][Cl] as solvent and acid ionic liquid [Bmim][HSO4] and CrCl3 as catalysts was studied. The effect of the temperature, reaction time,catalyst content, water content were investigated respectively. When [BmimJ[Cl] content is 4 g, MC content is 0.02 g, adding [Bmim][HSO4] content is 1 g and CrCl3 content is 0. 4 g at 130 ℃ , reaction time 4 h at normal conditions the molar ratio of 5-HMF is 37%. Experimental results demonstrate that the reaction system is active for the dehydration of MC into HMF under mild conditions.%研究了以自制的离子液体[Bmim][CI]为溶剂,酸性离子液体[Bmim-][HSO4]和CrCI3为催化剂,催化微晶纤维素脱水制备5-羟甲基糠醛的过程.分别考察了温度、时间、催化剂量、水含量对反应的影响.反应的优化条件为:常压下,[Bmim][CI]用量为4 g,微晶纤维素为0.02 g,在130℃下加入1 g[Bmim][HSO4]和0.4 g CrCI3,不加水,反应4h,5-HMF的摩尔收率可以达到37%.结果表明,在较温和的离子液体体系中直接转化微晶纤维素制得5-HMF是可行的.

  12. Physicochemical of microcrystalline cellulose from oil palm fronds as potential methylene blue adsorbents.

    Science.gov (United States)

    Hussin, M Hazwan; Pohan, Nurul Aqilah; Garba, Zaharaddeen N; Kassim, M Jain; Rahim, Afidah Abdul; Brosse, Nicolas; Yemloul, Mehdi; Fazita, M R Nurul; Haafiz, M K Mohamad

    2016-11-01

    The present study sheds light on the physical and chemical characteristics of microcrystalline cellulose (MCC) isolated from oil palm fronds (OPF) pulps. It was found that the OPF MCC was identified as cellulose II polymorph, with higher crystallinity index than OPF α-cellulose (CrIOPFMCC: 71%>CrIOPFα-cellulose: 47%). This indicates that the acid hydrolysis allows the production of cellulose that is highly crystalline. BET surface area of OPF MCC was found to be higher than OPF α-cellulose (SBETOPFMCC: 5.64m(2)g(-1)>SBETOPFα-cellulose:Qa(0) 2.04m(2)g(-1)), which corroborates their potential as an adsorbent. In batch adsorption studies, it was observed that the experimental data fit well with Langmuir adsorption isotherm in comparison to Freundlich isotherm. The monolayer adsorption capacity (Qa(0)) of OPF MCC was found to be around 51.811mgg(-1) and the experimental data fitted well to pseudo-second-order kinetic model.

  13. Isolation and characterization of microcrystalline cellulose from oil palm biomass residue.

    Science.gov (United States)

    Mohamad Haafiz, M K; Eichhorn, S J; Hassan, Azman; Jawaid, M

    2013-04-02

    In this work, we successfully isolated microcrystalline cellulose (MCC) from oil palm empty fruit bunch (OPEFB) fiber-total chlorine free (TCF) pulp using acid hydrolysis method. TCF pulp bleaching carried out using an oxygen-ozone-hydrogen peroxide bleaching sequence. Fourier transform infrared (FT-IR) spectroscopy indicates that acid hydrolysis does not affect the chemical structure of the cellulosic fragments. The morphology of the hydrolyzed MCC was investigated using scanning electron microscopy (SEM), showing a compact structure and a rough surface. Furthermore, atomic force microscopy (AFM) image of the surface indicates the presence of spherical features. X-ray diffraction (XRD) shows that the MCC produced is a cellulose-I polymorph, with 87% crystallinity. The MCC obtained from OPEFB-pulp is shown to have a good thermal stability. The potential for a range of applications such as green nano biocomposites reinforced with this form of MCC and pharmaceutical tableting material is discussed.

  14. Joint action of ultrasonic and Fe³⁺ to improve selectivity of acid hydrolysis for microcrystalline cellulose.

    Science.gov (United States)

    Li, Jinbao; Qiang, Dandan; Zhang, Meiyun; Xiu, Huijuan; Zhang, Xiangrong

    2015-09-20

    In this study, the combination of Fe(3+)/HCl and ultrasonic treatment was applied to selectively hydrolyze cellulose for the preparation of microcrystalline cellulose (MCC). It was found that the crystallinity and specific surface area of hydrocellulose samples were higher (78.92% and 2.23581 m(2)g(-1), respectively), compared with the method that only used Fe(3+)/HCl catalyst without ultrasonic treatment. Meanwhile, the hydrolysate can be extracted and reused for cellulose hydrolysis for three runs, which was effective in saving the dosage of chemicals and reducing the pollution of the environment without affecting the properties of hydrocellulose. Moreover, the increased concentration of total reducing sugar (TRS) after three runs may be used as a valuable source in biofuels production. The technology of cellulose hydrolysis, by retaining the crystalline region for MCC products while promoting hydrolysis of amorphous region for further utilization is of great novelty, which may prove valuable in converting biomass into chemicals and biofuels, environmentally and economically. Copyright © 2015 Elsevier Ltd. All rights reserved.

  15. Development and characterization of hybrid materials based on biodegradable PLA matrix, microcrystalline cellulose and organophilic silica

    Directory of Open Access Journals (Sweden)

    Fernanda Abbate dos Santos

    2014-10-01

    Full Text Available The goal of this work was to investigate the production and properties of hybrid materials based on poly(lactic acid (PLA, employing microcrystalline cellulose (MCC and organophilic silica (R972 as fillers. The composites were obtained by solution casting to form films. Each nanoparticle was incorporated at 3 wt. %, relative to the polymer matrix. In this experiment, four films were obtained (PLA, PLA/MCC, PLA/R972 and PLA/MCC/R972. The films properties were evaluated by X-ray diffractometry, nuclear magnetic resonance, Fourier transform infrared spectroscopy and mechanical properties. The results showed that each nanoparticle, added individually or both combined, had different effect on the final properties of the films. Microcrystalline cellulose can act as nucleating agent for the crystallization of PLA. Silica promoted an increase in rigidity, due to the strong intermolecular forces, while MCC addition promoted an increase in the molecular mobility of the polymeric chains. The PLA/MCC/R972 film showed the highest crystallinity degree and tensile modulus. This film presented a T1H value between both values found for PLA/MCC and PLA/R972 films. The results indicated that silica R972 could promote a decrease of the surface tension between PLA and cellulose.

  16. Small-angle x-ray scattering study on the structure of microcrystalline and nanofibrillated cellulose

    Energy Technology Data Exchange (ETDEWEB)

    Leppaenen, Kirsi; Pirkkalainen, Kari; Penttilae, Paavo; Serimaa, Ritva [Division of Materials Physics, Department of Physics, P.O.B. 64, FI-00014 University of Helsinki (Finland); Sievaenen, Jenni [VTT, Espoo (Finland); Kotelnikova, Nina, E-mail: kirsi.leppanen@helsinki.f [Institute of Macromolecular Compounds, Russian Academy of Sciences, Bolshoy pr. 31, St. Petersburg 199004 (Russian Federation)

    2010-10-01

    The effects of different solvents on the structure of microcrystalline and nanofibrillated cellulose (MCC, NFC) were studied using small-angle x-ray scattering (SAXS). MCC was immersed in water, ethanol, and acetone, and NFC was immersed only in water and ethanol, but studied also in the form of foam-like water-NFC-gel in wet, air-dried and re-wet states. The solvent affected the average chord length, which reveals the typical length scale of the structure of the sample: 2.4 {+-} 0.1 nm was obtained for MCC-water, 2.5 {+-} 0.1 nm for re-wet NFC-gel, 1.6 {+-} 0.1 nm for MCC-ethanol, 1.2 {+-} 0.1 nm for NFC-ethanol, and 1.3 {+-} 0.1 nm for MCC-acetone. The specific surface of cellulose increased strongly when MCC and NFC were immersed in the solvents compared to dry cellulose. The specific surface of cellulose was determined to be larger for NFC-water than MCC-water, and slightly larger for dry NFC powder than for dry MCC, which can be explained by the fact that the width of cellulose crystallites perpendicular to the cellulose chain direction was slightly larger in MCC than in NFC on the basis of wide-angle x-ray scattering results.

  17. Exploration of melt granulation technique for the development of coprocessed directly compressible adjuvant containing lactose and microcrystalline cellulose.

    Science.gov (United States)

    Gohe, Mukesh C; Jogani, Pranav D

    2003-01-01

    The objective of the present investigation was to prepare and evaluate lactose and microcrystalline cellulose based, directly compressible adjuvant using melt granulation technique. The percentage of polymer blend (PVP K 30 and PEG 4000; 5, 10, or 15%) and the polymer blend ratio (9:1, 1:1, or 1:9) were selected as independent variables in a 3(2) full factorial design. The lactose and microcrystalline cellulose blend (3:1) was mixed with the meltable binder on a water bath at 90 degrees C. The agglomerates were cooled to 35 degrees C and subsequently passed through 30 mesh. A batch containing 12.5% of the polymer blend containing 1:9 ratio of PVP:PEG was used for further studies. In an another 3(2) full factorial design, disintegrant (crospovidone, croscarmellose sodium, or sodium starch glycolate) and mode of addition of disintegrant (intragranular, extragranular, or combination of intragranular and extragranular) were used as independent variables. The agglomerates were evaluated for percentage fines and Carr's index. Tablets were prepared on a single-punch tablet machine, and they were evaluated for tensile strength, friability, and disintegration time. Regression analysis was carried out to evolve full and refined models. Contour plots are presented for graphical expression of the results. The use of composite index is demonstrated for the selection of an appropriate batch. The disintegration time of tablets reduced from 18 min to 6 min when 6% crospovidone was included in the product. The optimized adjuvant was characterized for particle size distribution, granular friability, Kawakita's and Kuno's equation, and dilution potential study. Turmeric, glycyrrhiza, acetaminophen, and metformin HCl were used as model drugs for the preparation of tablets. The present study underlines the fact that melt granulation technique may be adopted for the development of multifunctional directly compressible adjuvant for use in pharmaceuticals. The advantages of melt

  18. Fractal analysis of SEM images and mercury intrusion porosimetry data for the microstructural characterization of microcrystalline cellulose-based pellets

    Energy Technology Data Exchange (ETDEWEB)

    Gomez-Carracedo, A.; Alvarez-Lorenzo, C.; Coca, R.; Martinez-Pacheco, R.; Concheiro, A. [Departamento de Farmacia y Tecnologia Farmaceutica, Universidad de Santiago de Compostela, Santiago de Compostela 15782 (Spain); Gomez-Amoza, J.L. [Departamento de Farmacia y Tecnologia Farmaceutica, Universidad de Santiago de Compostela, Santiago de Compostela 15782 (Spain)], E-mail: joseluis.gomez.amoza@usc.es

    2009-01-15

    The microstructure of theophylline pellets prepared from microcrystalline cellulose, carbopol and dicalcium phosphate dihydrate, according to a mixture design, was characterized using textural analysis of gray-level scanning electron microscopy (SEM) images and thermodynamic analysis of the cumulative pore volume distribution obtained by mercury intrusion porosimetry. Surface roughness evaluated in terms of gray-level non-uniformity and fractal dimension of pellet surface depended on agglomeration phenomena during extrusion/spheronization. Pores at the surface, mainly 1-15 {mu}m in diameter, determined both the mechanism and the rate of theophylline release, and a strong negative correlation between the fractal geometry and the b parameter of the Weibull function was found for pellets containing >60% carbopol. Theophylline mean dissolution time from these pellets was about two to four times greater. Textural analysis of SEM micrographs and fractal analysis of mercury intrusion data are complementary techniques that enable complete characterization of multiparticulate drug dosage forms.

  19. Isolation and Characterization of Microcrystalline Cellulose (MCC from Rice Husk (RH

    Directory of Open Access Journals (Sweden)

    Ahmad Zuliahani

    2016-01-01

    Full Text Available Microcrystalline cellulose (MCC was extracted from local agricultural residues, rice husk (RH. RH undergone alkaline, bleaching and acid hydrolysis treatments. Nitric acid was used in the hydrolysis process as a potential acid to replace strong acids such as hydrochloric and sulphuric acids. Hydrolysis of RH was carried out by using different molarity of nitric and hydrochloric acids (control. The properties of MCC obtained such as % yield, crystallinity index (CrI and functional group present were studied. % yield shown a comparable result regardless of different acid used. Whilst Fourier transform infrared (FTIR spectroscopy showed the progressive removal of non-cellulosic constituents. X-ray diffraction (XRD analysis revealed that the crystallinity increased with successive treatments regardless different molarity and acids used. The results showed potential of nitric acid to be used in MCC isolation process.

  20. Statistical Optimization for Acid Hydrolysis of Microcrystalline Cellulose and Its Physiochemical Characterization by Using Metal Ion Catalyst

    Directory of Open Access Journals (Sweden)

    Md. Ziaul Karim

    2014-10-01

    Full Text Available Hydrolyzing the amorphous region while keeping the crystalline region unaltered is the key technology for producing nanocellulose. This study investigated if the dissolution properties of the amorphous region of microcrystalline cellulose can be enhanced in the presence of Fe3+ salt in acidic medium. The process parameters, including temperature, time and the concentration of metal chloride catalyst (FeCl3, were optimized by using the response surface methodology (RSM. The experimental observation demonstrated that temperature and time play vital roles in hydrolyzing the amorphous sections of cellulose. This would yield hydrocellulose with higher crystallinity. The factors that were varied for the production of hydrocellulose were the temperature (x1, time (x2 and FeCl3 catalyst concentration (x3. Responses were measured in terms of percentage of crystallinity (y1 and the yield (y2 of the prepared hydrocellulose. Relevant mathematical models were developed. Analysis of variance (ANOVA was carried out to obtain the most significant factors influencing the responses of the percentage of crystallinity and yield. Under optimum conditions, the percentage of crystallinity and yield were 83.46% and 86.98% respectively, at 90.95 °C, 6 h, with a catalyst concentration of 1 M. The physiochemical characteristics of the prepared hydrocellulose were determined in terms of XRD, SEM, TGA and FTIR analyses. The addition of FeCl3 salt in acid hydrolyzing medium is a novel technique for substantially increasing crystallinity with a significant morphological change.

  1. The Effect of Various Acids on Properties of Microcrystalline Cellulose (MCC) Extracted from Rice Husk (RH)

    Science.gov (United States)

    Nur Hanani, A. S.; Zuliahani, A.; Nawawi, W. I.; Razif, N.; Rozyanty, A. R.

    2017-05-01

    Microcrystalline cellulose (MCC) was successfully extracted from rice husk (RH) via acid hydrolysis process using nitric acid (HNO3) in comparison with sulphuric acid (H2SO4) and hydrochloric acid (HCl). MCC-RH extracted using HNO3 produced the highest percentage yield at 83.5% as compared to H2SO4 and HCl at 80.6% and 81.8% respectively. Analysis of Fourier Transform Infrared (FTIR) spectroscopy affirmed the successive elimination of non-cellulosic material from RH cellulose resulting highly purified MCC-RH. X-ray Diffraction (XRD) analysis showed MCC-RH treated with HCl gives the highest crystallinity index value of 54.2% while HNO3 and H2SO4 produced comparable results of 52.4% and 49.7% respectively. The results indicate successive extraction of MCC-RH using HNO3 that has great potential to replace strong acid such as H2SO4 and HCl in acid hydrolysis.

  2. Effect of Mild Acid Hydrolysis Parameters on Properties of Microcrystalline Cellulose

    Directory of Open Access Journals (Sweden)

    Kari Mikael Vanhatalo

    2014-06-01

    Full Text Available The effects of mild kraft pulp hydrolysis conditions (reaction time, temperature, pulp consistency, and acid dosage with sulfuric acid (H2SO4 on the properties of microcrystalline cellulose (MCC were investigated. The degree of polymerization (DP of cellulose rapidly decreased at the initiation of hydrolysis and leveled off after a certain reaction time, depending on the hydrolysis conditions. The intensity of the hydrolysis treatment greatly affected the cellulose particle size. Compared to the intensive treatment, the mild conditions resulted in a broader particle size distribution, while smaller particles with a narrow size distribution were obtained under severe conditions. However, the particle size leveled off at a hydrolysis factor (P-factor of 300. The results suggest that after a certain P-factor (300, severe hydrolysis conditions have no advantage over mild ones as related to the MCC particle properties. Because of favourable reaction conditions (short delay time, moderate temperature, and small amounts of chemicals, this method can be implemented on an industrial scale in a chemical pulp mill.

  3. Dissolution profile of novel composite pellet cores based on different ratios of microcrystalline cellulose and isomalt.

    Science.gov (United States)

    Luhn, Oliver; Kállai, Nikolett; Nagy, Zsombor Kristóf; Kovács, Kristóf; Fritzsching, Bodo; Klebovich, Imre; Antal, István

    2012-08-01

    There is a growing interest towards the application of inert cores as starting materials for pharmaceutical pellet manufacturing. They serve as alternatives to develop and adapt a relatively simple manufacturing technology compared with an extrusion/spheronisation process. The major objective of this study was to investigate the effect of the compositions of core materials on the drug release profile. Pure microcrystalline cellulose (MCC), isomalt and different types of novel composite MCC-isomalt cores were layered with model drug (sodium diclofenac) and were coated with acrylic polymer. The effect of the osmolality in the gastrointestinal tract was simulated using glucose as osmotically active agent during in vitro dissolution tests. The results demonstrated the dependence of drug dissolution profile on the ratio of MCC and isomalt in the core and the influence of osmotic properties of the dissolution medium. Isomalt used in the composite core was able to decrease the vulnerability of the dissolution kinetics to the changes in the osmotic environment.

  4. Microcrystalline cellulose: Isolation, characterization and bio-composites application-A review.

    Science.gov (United States)

    Trache, Djalal; Hussin, M Hazwan; Hui Chuin, Caryn Tan; Sabar, Sumiyyah; Fazita, M R Nurul; Taiwo, Owolabi F A; Hassan, T M; Haafiz, M K Mohamad

    2016-12-01

    Considering its widespread usage in various fields, such as food, pharmaceutical, medical, cosmetic and polymer composites industries, microcrystalline cellulose (MCC) is becoming impellent due to increasing demand of alternatives to non-renewable and scarce fossil materials. Although it still suffers from some drawbacks, MCC has recently gained more interest owing to its renewability, non-toxicity, economic value, biodegradability, high mechanical properties, high surface area and biocompatibility. New sources, new isolation processes, and new treatments are currently under development to satisfy the increasing demand of producing new types of MCC-based materials on an industrial scale. Therefore, this review assembles the current knowledge on the isolation of MCC from different sources using various procedures, its characterization, and its application in bio-composites. Challenges and future opportunities of MCC-based composites are discussed as well as obstacles remaining for their extensive uses.

  5. Microcrystalline-cellulose and polypropylene based composite: A simple, selective and effective material for microwavable packaging.

    Science.gov (United States)

    Ummartyotin, S; Pechyen, C

    2016-05-20

    Cellulose based composite was successfully designed as active packaging with additional feature of microwavable properties. Small amount of cellulose with 10 μm in diameter was integrated into polypropylene matrix. The use of maleic anhydride was employed as coupling agent. Thermal and mechanical properties of cellulose based composite were superior depending on polypropylene matrix. Crystallization temperature and compressive strength were estimated to be 130 °C and 5.5 MPa. The crystal formation and its percentage were therefore estimated to be 50% and it can be predicted on the feasibility of microwavable packaging. Morphological properties of cellulose based composite presented the good distribution and excellent uniformity. It was remarkable to note that cellulose derived from cotton can be prepared as composite with polypropylene matrix. It can be used as packaging for microwave application.

  6. Effect of phosphoric acid pretreatment on enzymatic hydrolysis of microcrystalline cellulose.

    Science.gov (United States)

    Zhang, Juanhua; Zhang, Beixiao; Zhang, Jingqiang; Lin, Lu; Liu, Shijie; Ouyang, Pingkai

    2010-01-01

    Microcrystalline cellulose (MCC) was pretreated with phosphoric acid at 323K for 10h. X-ray diffraction (XRD) and Atomic Force Microscope (AFM) analyses revealed that the fiber surface morphology of pretreated MCC (P-MCC) were uneven and rough with the crystalline diffraction peaks of P-MCC decreased to a distinct range. The X-ray Photoelectron Spectroscopy (XPS) analysis showed that the uneven and rough surface of P-MCC could enhance the adsorption of cellulose to the molecular surface of cellulose, which is one of the key factors affecting enzymatic hydrolysis of cellulose. A reversible first order kinetics was employed to describe the adsorption kinetics of cellulase to MCC and P-MCC, and the adsorption rate constants of MCC and P-MCC were found to be 0.016, 0.024, 0.041, and 0.095, 0.149, 0.218min(-1), respectively at 278K, 293K and 308K. The activation energies of MCC and P-MCC hydrolysis reactions were found to be 22.257 and 19.721kJ mol(-1). The major hydrolysis products of MCC and P-MCC were cellobiose and glucose. Hydrolysis of MCC for 120h resulted in yields of glucose (7.21%), cellobiose (13.16%) and total sugars (20.37%). However, after the pretreatment with phosphoric acid, the corresponding sugar yields resulted from enzymatic hydrolysis of P-MCC were increased to 24.10%, 41.42%, and 65.52%; respectively, which were 3.34, 3.15, and 3.22 times of the sugars yields from enzymatic hydrolysis of MCC. Copyright 2010 Elsevier Inc. All rights reserved.

  7. Composite edible films based on hydroxypropyl methyl cellulose reinforced with microcrystalline cellulose nanoparticles

    Science.gov (United States)

    It has been stated that hydroxypropyl methyl cellulose (HPMC) based films have promising applications in the food industry because of their environmental appeal, low cost, flexibility and transparency. Nevertheless, their mechanical and moisture barrier properties should be improved. The aim of th...

  8. Hydrolysis of microcrystalline cellulose using functionalized Bronsted acidic ionic liquids - A comparative study.

    Science.gov (United States)

    Parveen, Firdaus; Patra, Tanmoy; Upadhyayula, Sreedevi

    2016-01-01

    Cellulose conversion to platform chemicals is required to meet the demands of increasing population and modernization of the world. Hydrolysis of microcrystalline cellulose was studied with SO3H, COOH and OH functionalized imidazole based ionic liquid using 1-butyl-3-methylimidazolium chloride [BMIM]Cl as a solvent. The influence of temperature, time, acidity of ionic liquids and catalyst loading was studied on hydrolysis reaction. The maximum %TRS yield 85%, was obtained at 100°C and 90min with 0.2g of SO3H functionalized ionic liquid. UV-vis spectroscopy using 4-nitro aniline as an indicator was performed to find out the Hammett function of ionic liquid and acidity trends are as follows: SO3H>COOH>OH. Density functional theory (DFT) calculations were performed to optimize the ionic liquid and their conjugate bases at B3LYP 6-311G++ (d, p) level using Gaussian 09 program. Theoretical findings are in agreement with the experimental results. Copyright © 2015 Elsevier Ltd. All rights reserved.

  9. The influence of the moisture content of microcrystalline cellulose on the coating process in a fluidized bed

    Directory of Open Access Journals (Sweden)

    Silva O. S.

    2004-01-01

    Full Text Available The objective of this work was to study the coating of microcrystalline cellulose with a polymeric suspension in a fluidized bed. The coating operation was carried out using a fluidized bed with top spraying by a double-fluid nozzle. The fluidized bed consists of a cylindrical column made of plexiglass with a height of 0.6 m and an inner diameter of 0.14 m. The polymeric coating suspension was formulated using Eudragit® as the basic component. As the quality of the coating product is greatly affected by the spraying characteristics, the influence of the flow rate of the coating suspension and the moisture content of the particles on the agglomeration index and efficiency of the process of coating microcrystalline cellulose was analyzed.

  10. Preparation, Characterization, and Cationic Functionalization of Cellulose-Based Aerogels for Wastewater Clarification

    Directory of Open Access Journals (Sweden)

    Yang Hu

    2016-01-01

    Full Text Available Aerogels are a series of materials with porous structure and light weight which can be applied to many industrial divisions as insulators, sensors, absorbents, and cushions. In this study, cellulose-based aerogels (aerocelluloses were prepared from cellulosic material (microcrystalline cellulose in sodium hydroxide/water solvent system followed by supercritical drying operation. The average specific surface area of aerocelluloses was 124 m2/g. The nitrogen gas (N2 adsorption/desorption isotherms revealed type H1 hysteresis loops for aerocelluloses, suggesting that aerocelluloses may possess a porous structure with cylindrically shaped pores open on both ends. FTIR and XRD analyses showed that the crystallinity of aerocelluloses was significantly decreased as compared to microcrystalline cellulose and that aerocelluloses exhibited a crystalline structure of cellulose II as compared to microcrystalline cellulose (cellulose I. To perform cationic functionalization, a cationic agent, (3-chloro-2-hydroxypropyl trimethylammonium chloride, was used to introduce positively charged sites on aerocelluloses. The cationized aerocelluloses exhibited a strong ability to remove anionic dyes from wastewater. Highly porous and low cost aerocelluloses prepared in this study would be also promising as a fast absorbent for environmental pollutants.

  11. Enhanced Photocatalytic Activity of CdS-Decorated TiO2/Carbon Core-Shell Microspheres Derived from Microcrystalline Cellulose

    Directory of Open Access Journals (Sweden)

    Xin Liu

    2016-03-01

    Full Text Available The fabrication of reusable and biodegradation materials from renewable resources such as cellulose is essential for a sustainable world. The core-shell structured CdS-decorated TiO2/Carbon microspheres (CdS/TiO2/Carbon MS photocatalyst was synthesized with controlled hydrolysis and a novel sonochemical method. It was prepared by using crosslinked microcrystalline cellulose as the core, tetrabutyl titanate as the titania source and CdS as the photosensitizer. The morphology, chemical structure and properties of the obtained material were characterized by many means. Additionally, the photocatalytic activity of the CdS/TiO2/Carbon MS was evaluated by the photodegradation efficiency of Rhodamine B solution, which reached 95.24% under visible light irradiation. This study demonstrated the excellent photocatalytic performance of CdS/TiO2/Carbon MS, which might have promising applications in environmental treatments.

  12. Evaluation of drug release from coated pellets based on isomalt, sugar, and microcrystalline cellulose inert cores.

    Science.gov (United States)

    Kállai, Nikolett; Luhn, Oliver; Dredán, Judit; Kovács, Kristóf; Lengyel, Miléna; Antal, István

    2010-03-01

    The objective of the present study was to investigate the effect of the pellet core materials isomalt, sugar, and microcrystalline cellulose on the in vitro drug release kinetics of coated sustained-release pellets as well as to evaluate the influence of different ratios of polymethacrylate copolymers exhibiting different permeability characteristics on the drug release rate. For characterization of the drug release process of pellets, the effect of osmolality was studied using glucose as an osmotically active agent in the dissolution medium. The pellet cores were layered with diclofenac sodium as model drug and coated with different ratios of Eudragit RS30D and Eudragit RL30D (ERS and ERL; 0:1 and 0.5:0.5 and 1:0 ratio) in a fluid bed apparatus. Physical characteristics such as mechanical strength, shape, and size proved that the inert cores were adequate for further processing. The in vitro dissolution tests were performed using a USP Apparatus I (basket method). The results demonstrated that, besides the ratio of the coating polymers (ERS/ERL), the release mechanism was also influenced by the type of starter core used. Sugar- and isomalt-type pellet cores demonstrated similar drug release profiles.

  13. Evaluation of several microcrystalline celluloses obtained from agricultural by-products

    Directory of Open Access Journals (Sweden)

    John Rojas

    2011-01-01

    Full Text Available Microcrystalline cellulose (MCCI has been widely used as an excipient for direct compression due to its good flowability, compressibility, and compactibility. In this study, MCCI was obtained from agricultural by-products, such as corn cob, sugar cane bagasse, rice husk, and cotton by pursuing acid hydrolysis, neutralization, clarification, and drying steps. Further, infrared spectroscopy (IR, X-ray diffraction (XRD, optical microscopy, degree of polymerization (DP, and powder and tableting properties were evaluated and compared to those of Avicel PH101, Avicel PH102, and Avicel PH200. Except for the commercial products, all materials showed a DP from 55 to 97. Particles of commercial products and corn cob had an irregular shape, whereas bagasse particles were elongated and thick. Rice and cotton particles exhibited a flake-like and fiber-like shape, respectively. MCCI as obtained from rice husk and cotton was the most densified material, while that produced from corn cob and bagasse was bulky, porous, and more compressible. All products had a moisture content of less than 10% and yields from 7.4% to 60.4%. MCCI as obtained from bagasse was the most porous and compressible material among all materials. This product also showed the best tableting properties along with Avicel products. Likewise, all MCCI products obtained from the above-mentioned sources showed a more rapid disintegration time than that of Avicel products. These materials can be used as a potential source of MCCI in the production of solid dosage forms.

  14. Evaluation of several microcrystalline celluloses obtained from agricultural by-products.

    Science.gov (United States)

    Rojas, John; Lopez, Alvin; Guisao, Santiago; Ortiz, Carlos

    2011-07-01

    Microcrystalline cellulose (MCCI) has been widely used as an excipient for direct compression due to its good flowability, compressibility, and compactibility. In this study, MCCI was obtained from agricultural by-products, such as corn cob, sugar cane bagasse, rice husk, and cotton by pursuing acid hydrolysis, neutralization, clarification, and drying steps. Further, infrared spectroscopy (IR), X-ray diffraction (XRD), optical microscopy, degree of polymerization (DP), and powder and tableting properties were evaluated and compared to those of Avicel PH101, Avicel PH102, and Avicel PH200. Except for the commercial products, all materials showed a DP from 55 to 97. Particles of commercial products and corn cob had an irregular shape, whereas bagasse particles were elongated and thick. Rice and cotton particles exhibited a flake-like and fiber-like shape, respectively. MCCI as obtained from rice husk and cotton was the most densified material, while that produced from corn cob and bagasse was bulky, porous, and more compressible. All products had a moisture content of less than 10% and yields from 7.4% to 60.4%. MCCI as obtained from bagasse was the most porous and compressible material among all materials. This product also showed the best tableting properties along with Avicel products. Likewise, all MCCI products obtained from the above-mentioned sources showed a more rapid disintegration time than that of Avicel products. These materials can be used as a potential source of MCCI in the production of solid dosage forms.

  15. Impact of microcrystalline cellulose material attributes: a case study on continuous twin screw granulation.

    Science.gov (United States)

    Fonteyne, Margot; Correia, Ana; De Plecker, Sofie; Vercruysse, Jurgen; Ilić, Ilija; Zhou, Qi; Vervaet, Chris; Remon, Jean Paul; Onofre, Fernanda; Bulone, Vincent; De Beer, Thomas

    2015-01-30

    The International Conference on Harmonisation (ICH) states in its Q8 'Pharmaceutical Development' guideline that the manufacturer of pharmaceuticals should have an enhanced knowledge of the product performance over a range of material attributes, manufacturing process options and process parameters. The present case study evaluates the effect of unspecified variability of raw material properties upon the quality attributes of granules; produced using a continuous from-powder-to-tablet wet granulation line (ConsiGma™ 25). The impact of different material attributes of six samples of microcrystalline cellulose (MCC) was investigated. During a blind study the different samples of MCC were used separately and the resulting granules were evaluated in order to identify the differences between the six samples. Variation in size distribution due to varying water binding capacity of the MCC samples was observed. The cause of this different water binding capacity was investigated and was caused by a different degree of crystallinity. Afterwards, an experimental design was conducted in order to evaluate the effect of both product and process variability upon the granule size distribution. This model was used in order to calculate the required process parameters to obtain a preset granule size distribution regardless of the type of MCC used. The difference in water binding capacity and its effect on granular properties was still present when combining the MCC grades with different binders. Copyright © 2014 Elsevier B.V. All rights reserved.

  16. Supercritical water treatment for cello-oligosaccharide production from microcrystalline cellulose.

    Science.gov (United States)

    Tolonen, Lasse K; Juvonen, Minna; Niemelä, Klaus; Mikkelson, Atte; Tenkanen, Maija; Sixta, Herbert

    2015-01-12

    Microcrystalline cellulose was treated in supercritical water at 380 °C and at a pressure of 250 bar for 0.2, 0.4, and 0.6s. The yield of the ambient-water-insoluble precipitate and its average molar mass decreased with an extended treatment time. The highest yield of 42 wt% for DP2-9 cello-oligosaccharides was achieved after the 0.4s treatment. The reaction products included also 11 wt% ambient-water-insoluble precipitate with a DP(w) of 16, and 6.1 wt% monomeric sugars, and 37 wt% unidentified degradation products. Oligo- and monosaccharide-derived dehydration and retro-aldol fragmentation products were analyzed via a combination of HPAEC-PAD-MS, ESI-MS/MS, and GC-MS techniques. The total amount of degradation products increased with treatment time, and fragmented (glucosyl(n)-erythrose, glucosyl(n)-glycolaldehyde), and dehydrated (glucosyl(n)-levoglucosan) were identified as the main oligomeric degradation products from the cello-oligosaccharides.

  17. [Quality by design based high shear wet granulation process development for the microcrystalline cellulose].

    Science.gov (United States)

    Luo, Gan; Xu, Bing; Sun, Fei; Cui, Xiang-long; Shi, Xin-yuan; Qiao, Yan-jiang

    2015-03-01

    The design space of the high shear wet granulation process was established and validated within the framework of quality by design (QbD). The system of microcrystalline cellulose-de-ioned water was used in this study. The median granule size and bulk density of granules were identified as critical quality attributes. Plackeet-Burmann experimental design was used to screen these factors as follows: dry mixing time, the impeller and chopper speed of dry mixing, water amount, water addition time, wet massing time, the impeller and chopper speed of wet massing and drying time. And the optimization was implemented with the central composite experimental design based on screened critical process parameters. The design space of the high shear wet granulation process was established based on the quadratic polynomial regression model. Since the P-values of both models were less than 0.05 and values of lack of fit were more than 0.1, the relationship between critical quality attributes and critical process parameters could be well described by the two models. The reliability of design space, illustrated by overlay plot, was improved with the addition of 95% confidence interval. For those granules whose process parameters were in the design space, the granule size could be controlled within 250 to 355 μm, and the bulk density could be controlled within a range of 0.4 to 0.6 g x cm(-3). The robustness and flexibility of the high shear wet granulation process have been enhanced via the establishment of the design space based on the QbD concept.

  18. Influence of alkaline hydrogen peroxide pre-hydrolysis on the isolation of microcrystalline cellulose from oil palm fronds.

    Science.gov (United States)

    Owolabi, Abdulwahab F; Haafiz, M K Mohamad; Hossain, Md Sohrab; Hussin, M Hazwan; Fazita, M R Nurul

    2017-02-01

    In the present study, microcrystalline cellulose (MCC) was isolated from oil palm fronds (OPF) using chemo-mechanical process. Wherein, alkaline hydrogen peroxide (AHP) was utilized to extract OPF fibre at different AHP concentrations. The OPF pulp fibre was then bleached with acidified sodium chlorite solution followed by the acid hydrolysis using hydrochloric acid. Several analytical methods were conducted to determine the influence of AHP concentration on thermal properties, morphological properties, microscopic and crystalline behaviour of isolated MCC. Results showed that the MCC extracted from OPF fibres had fibre diameters of 7.55-9.11nm. X-ray diffraction (XRD) analyses revealed that the obtained microcrystalline fibre had both celluloses I and cellulose II polymorphs structure, depending on the AHP concentrations. The Fourier transmission infrared (FTIR) analyses showed that the AHP pre-hydrolysis was successfully removed hemicelluloses and lignin from the OPF fibre. The crystallinity of the MCC was increased with the AHP concentrations. The degradation temperature of MCC was about 300°C. The finding of the present study showed that pre-treatment process potentially influenced the quality of the isolation of MCC from oil palm fronds. Copyright © 2016 Elsevier B.V. All rights reserved.

  19. Photophysical Studies of a New Water Soluble Indocarbocyanine Dye Adsorbed onto Microcrystalline Cellulose and b-Cyclodextrin

    Directory of Open Access Journals (Sweden)

    Luis F. Vieira Ferreira

    2013-05-01

    Full Text Available A water-soluble indocarbocyanine dye was synthesized and its photophysics were studied for the first time on two solid hosts, microcrystalline cellulose and b-cyclodextrin, as well as in homogeneous media. The inclusion of the indocarbocyanine moiety onto microcrystalline cellulose increased the dye aggregation with both H and J aggregates being formed. Adsorption on b-cyclodextrin enhanced aggregation in a similar way. The fluorescence quantum yields were determined for the powdered samples of the cyanine dye on the two hosts and a significant increase was observed relative to homogeneous solution. A remarkable concentration dependence was also detected in both cases. A lifetime distribution analysis has shown that the indocarbocyanine dye mainly occupies the amorphous part of cellulose and is not entrapped in the crystalline part of this host. In the b-CD case, the adsorption occurs outside the host cavity. In both hosts a strong concentration quenching effect is observed and only monomers emit. Both adsorptions may be explained by stereochemical constraints imposed by the two long sulphoethyl tails linked to nitrogen atoms of the indocarbocyanine dye.

  20. The effect of pulping concentration treatment on the properties of microcrystalline cellulose powder obtained from waste paper.

    Science.gov (United States)

    Okwonna, Okumneme O

    2013-10-15

    Microcrystalline cellulose (MCC) powder was isolated from three grades of waste paper: book, Groundwood/Newsprint and paperboard, through the processes of pulping and hydrolysis. Pulping treatment on these grades of waste paper was done using varying concentrations of caustic soda. Effects of the concentration of the pulping medium on the thermal and kinetic properties were investigated. Also determined were the effects of this on the physico-chemical properties. The chemical structure was characterized using an infrared spectroscopy (FTIR). Results showed these properties to be affected by the concentration of the pulping medium. Copyright © 2013 Elsevier Ltd. All rights reserved.

  1. MORPHOLOGY, IN VITRO - DEGRADATION AND DRUG RELEASE PROFILE OF POLY (ETHYLENE-CO-VINYL ACETATE / MICROCRYSTALLINE CELLULOSE ACETATE

    Directory of Open Access Journals (Sweden)

    K. Lakshmi Narayana

    2011-06-01

    Full Text Available Microcrystalline cellulose acetate (MCC was incorporated in poly (ethylene-co-vinyl acetate (EVA at different loading. The morphology, swelling properties and drug release profile were studied with respect to MCC loading to study its potential application as ocular inserts. The XRD patterns showed a good compatibility between the components. However swelling ratio and in-vitro degradation of EVA increase with MCC loading. This has been explained in terms of the hygroscopic nature of cellulose acetate. The study shows that EVA/MCC system can be tuned in terms of important parameters such as swelling behavior, in vitro release and degradation by varying blend composition, thus fulfilling specific biomedical requirements.

  2. Functionalization of Microcrystalline Cellulose with N,N-dimethyldodecylamine for the Removal of Congo Red Dye from an Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Dongying Hu

    2014-08-01

    Full Text Available Microcrystalline cellulose (MCC was functionalized with quaternary amine groups for use as an adsorbent to remove Congo Red dye (CR from aqueous solution. The ultrasonic pretreatment of MCC was investigated during its functionalization. Characterization was conducted using infrared spectroscopy (FT-IR, X-ray photoelectron spectroscopy (XPS, X-ray diffraction (XRD, and scanning electron microscopy (SEM. The batch adsorption of the functionalized MCC was studied to evaluate the effects of dye concentration, pH of solution, temperature, and NaCl concentration on the adsorption CR. The adsorbent (FM-1 obtained using ultrasonic pretreatment of MCC under 10.8 kJ•g–1 exhibited an adsorption capacity of 304 mg•g–1 at initial pH under a dose of 0.1 g•L–1 and initial concentration of 80 mg•L–1. After functionalization, the FT-IR and XPS results indicated that the quaternary amine group was successfully grafted onto the cellulose, the surface was transformed to be coarse and porous, and the crystalline structure of the original cellulose was disrupted. FM-1 has been shown to be a promising and efficient adsorbent for the removal of CR from an aqueous solution.

  3. Enzymatic properties of Thermoanaerobacterium thermosaccharolyticum β-glucosidase fused to Clostridium cellulovorans cellulose binding domain and its application in hydrolysis of microcrystalline cellulose.

    Science.gov (United States)

    Zhao, Linguo; Pang, Qian; Xie, Jingcong; Pei, Jianjun; Wang, Fei; Fan, Song

    2013-11-14

    The complete degradation of the cellulose requires the synergistic action of endo-β-glucanase, exo-β-glucanase, and β-glucosidase. But endo-β-glucanase and exo-β-glucanase can be recovered by solid-liquid separation in cellulose hydrolysis by their cellulose binding domain (CBD), however, the β-glucosidases cannot be recovered because of most β-glucosidases without the CBD, so additional β-glucosidases are necessary for the next cellulose degradation. This will increase the cost of cellulose degradation. The glucose-tolerant β-glucosidase (BGL) from Thermoanaerobacterium thermosaccharolyticum DSM 571 was fused with cellulose binding domain (CBD) of Clostridium cellulovorans cellulosome anchoring protein by a peptide linker. The fusion enzyme (BGL-CBD) gene was overexpressed in Escherichia coli with the maximum β-glucosidase activity of 17 U/mL. Recombinant BGL-CBD was purified by heat treatment and following by Ni-NTA affinity. The enzymatic characteristics of the BGL-CBD showed optimal activities at pH 6.0 and 65°C. The fusion of CBD structure enhanced the hydrolytic efficiency of the BGL-CBD against cellobiose, which displayed a 6-fold increase in Vmax/Km in comparison with the BGL. A gram of cellulose was found to absorb 643 U of the fusion enzyme (BGL-CBD) in pH 6.0 at 50°C for 25 min with a high immobilization efficiency of 90%. Using the BGL-CBD as the catalyst, the yield of glucose reached a maximum of 90% from 100 g/L cellobiose and the BGL-CBD could retain over 85% activity after five batches with the yield of glucose all above 70%. The performance of the BGL-CBD on microcrystalline cellulose was also studied. The yield of the glucose was increased from 47% to 58% by adding the BGL-CBD to the cellulase, instead of adding the Novozyme 188. The hydrolytic activity of BGL-CBD is greater than that of the Novozyme 188 in cellulose degradation. The article provides a prospect to decrease significantly the operational cost of the hydrolysis process.

  4. Bioaugmented hydrogen production from microcrystalline cellulose using co-culture - Clostridium acetobutylicumX{sub 9} and Ethanoigenens harbinenseB{sub 49}

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Aijie; Ren, Nanqi; Shi, Yinguen [School of Municipal and Environmental Engineering, Harbin Institute of Technology, P.O. Box 2614, 202 Haihe Road, Harbin 150090 (China); Lee, Duu-Jong [School of Municipal and Environmental Engineering, Harbin Institute of Technology, P.O. Box 2614, 202 Haihe Road, Harbin 150090 (China); Department of Chemical Engineering, National Taiwan University, Taipei (China)

    2008-01-15

    Dark fermentation of microcrystalline cellulose to produce biohydrogen using mono-culture or co-culture of isolated strains was studied. A strain (X{sub 9}) with high hydrogen yield from microcrystalline cellulose was isolated and identified to be closely affiliated with Clostridium acetobutylicum, ATCC 824. At 37{sup o}C and pH 5.0, the mono-culture of X{sub 9} yields hydrogen with a 5-h time lag and end liquid products primarily of acetate and butyrate. The co-culture of X{sub 9} with another strain, Ethanoigenens harbinenseB{sub 49}, which can produce hydrogen efficiently from monosaccharides but directly from microcrystalline cellulose, produced more efficiently the biohydrogen via ethanol-type fermentation metabolism compared with mono-culture X{sub 9} test. Bioaugmentation with X{sub 9}+B{sub 49} improved cellulose hydrolysis and subsequent hydrogen production rates as compared with that of mono-culture bioaugmentation with X{sub 9}. (author)

  5. Enzymatic membrane reactor for full saccharification of ionic liquid-pretreated microcrystalline cellulose.

    Science.gov (United States)

    Lozano, Pedro; Bernal, Berenice; Jara, Antonio G; Belleville, Marie-Pierre

    2014-01-01

    Ultrafiltration reactors based on polymeric or ceramic membranes were shown to be suitable catalytic systems for fast enzymatic saccharification of cellulose, allowing the full recovery and reuse of enzymes. By pre-treating cellulose with the IL 1-butyl-3-methylimidazolium chloride, the suitability of this substrate for enzymatic saccharification in a reactor based on polymeric ultrafiltration membranes was demonstrated, leading to 95% cellulose hydrolysis in 4h at 50°C. The filtration process gave a clear glucose solution (up to 113 mM) at constant permeate flow (24.7 L h(-1) m(-2)), allowing the enzyme to be reused for 9 operation cycles under semi-continuous operation, without any loss of enzyme activity. Under continuous operation mode and using ceramic ultrafiltration membranes at different residence times, the enzymatic reactor showed constant profiles in both the permeate flow rate and the glucose concentration, demonstrating the excellent suitability of the proposed approach for the saccharification of cellulose.

  6. Controlled silver delivery by silver-cellulose nanocomposites prepared by a one-pot green synthesis assisted by microwaves

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Ana Rosa; Unali, Gianfranco, E-mail: ana.rosa.silva@ua.pt [Structured Materials Expertise Group, Unilever Discover Port Sunlight, Quarry Road East, Bebington CH63 3JW (United Kingdom)

    2011-08-05

    Controlled silver release from cellulosic nanocomposites was achieved by synthesizing silver nanoparticles, under microwave heating for 1-15 min, in a one-pot, versatile and sustainable process in which microcrystalline cellulose simultaneously functions as reducing, stabilizing and supporting agent in water; chitin, starch and other cellulose derivatives could also be used as reducing, stabilizing and supporting agents for silver nanoparticles and the method was also found to be extensible to the preparation of noble metal (Au, Pt) and metal oxide nanoparticle (ZnO, Cu, CuO and Cu{sub 2}O) nanocomposites.

  7. Preparation of microcrystalline mixtures for calibration of laser microbeam ionisation mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Ignatova, V. E-mail: velislav@uia.ua.ac.be; Vaeck, L. van; Ham, R. van; Adriaens, A.; Adams, F

    2002-03-11

    In this paper we describe the optimized experimental procedure and the apparatus to prepare microcrystalline samples of inorganic salt mixtures to be used as molecular standards in Laser Microprobe Mass Spectrometry (LMMS). Experimental data show the suitability of the approach for preparation of solid mixtures of various inorganic salts. The structure and homogeneity of the samples are studied by Scanning Electron Microscopy and Fourier Transform LMMS. Specifically, the in-sample and between-sample reproducibility reveals that the method allows the local sample composition to be sufficiently homogeneous for subsequent use in the semi-quantitative calibration of the molecular signals in LMMS.

  8. Preparation of microcrystalline mixtures for calibration of laser microbeam ionisation mass spectrometry

    CERN Document Server

    Ignatova, V A; Ham, R V; Adriaens, A; Adams, F

    2002-01-01

    In this paper we describe the optimized experimental procedure and the apparatus to prepare microcrystalline samples of inorganic salt mixtures to be used as molecular standards in Laser Microprobe Mass Spectrometry (LMMS). Experimental data show the suitability of the approach for preparation of solid mixtures of various inorganic salts. The structure and homogeneity of the samples are studied by Scanning Electron Microscopy and Fourier Transform LMMS. Specifically, the in-sample and between-sample reproducibility reveals that the method allows the local sample composition to be sufficiently homogeneous for subsequent use in the semi-quantitative calibration of the molecular signals in LMMS.

  9. To Evaluate the Effect of Solvents and Different Relative Humidity Conditions on Thermal and Rheological Properties of Microcrystalline Cellulose 101 Using METHOCEL™ E15LV as a Binder.

    Science.gov (United States)

    Jagia, Moksh; Trivedi, Maitri; Dave, Rutesh H

    2016-08-01

    The solvent used for preparing the binder solution in wet granulation can affect the granulation end point and also impact the thermal, rheological, and flow properties of the granules. The present study investigates the effect of solvents and percentage relative humidity (RH) on the granules of microcrystalline cellulose (MCC) with hydroxypropyl methyl cellulose (HPMC) as the binder. MCC was granulated using 2.5% w/w binder solution in water and ethanol/water mixture (80:20 v/v). Prepared granules were dried until constant percentage loss on drying, sieved, and further analyzed. Dried granules were exposed to different percentage RH for 48 h at room temperature. Powder rheometer was used for the rheological and flow characterization, while thermal effusivity and differential scanning calorimeter were used for thermal analysis. The thermal effusivity values for the wet granules showed a sharp increase beginning 50% w/w binder solution in both cases, which reflected the over-wetting of granules. Ethanol/water solvent batches showed greater resistance to flow as compared to the water solvent batches in the wet granule stage, while the reverse was true for the dried granule stage, as evident from the basic flowability energy values. Although the solvents used affected the equilibration kinetics of moisture content, the RH-exposed granules remained unaffected in their flow properties in both cases. This study indicates that the solvents play a vital role on the rheology and flow properties of MCC granules, while the different RH conditions have little or no effect on them for the above combination of solvent and binder.

  10. Dissolution and regeneration of microcrystalline cellulose in 1-ethyl-3-methylimidazolium diethylphosphate%微晶纤维素在EMIM-DEP中的溶解与再生

    Institute of Scientific and Technical Information of China (English)

    陶伟娜; 王少君; 李飞

    2012-01-01

    1-Ethyl-3-methylimidazolium diethylphosphate (EMIM-DEP) is synthesized with microwave method and is used to dissolve microcrystalline cellulose in this study. Its dissolution process is observed by polarizing microscope. With the rise of temperature the solubility of cellulose increases. Ultrasonic auxiliary can improve well the solubility of microcrystalline cellulose in ionic liquids. The regenerated cellulose is characterized by FT-IR, XRD, SEM and TGA. The results show that the microcrystalline cellulose in EMIM-DEP is dissolved directly without derivative reaction. The regenerated cellulose is changed from cellulose I into cellulose II in crystal style. Recovered ionic liquid has no change in structure and can be reused with good dissolving ability for microcrystalline cellulose.%通过微波法合成1-乙基-3-甲基咪唑磷酸二乙酯离子液体(EMIM-DEP)并用其溶解微晶纤维素.用偏光显微镜观察微晶纤维素在离子液体中的溶解.随温度的升高纤维素的溶解度增加,超声辅助可以很好地提高微晶纤维素在离子液体中的溶解度.溶解之后再生的纤维素通过红外光谱(FT-IR)、X-射线衍射(XRD)、扫描电镜(SEM)和热重分析(TGA)表征,结果显示微晶纤维素在EMIM-DEP中是直接溶解没有发生衍生反应;再生的纤维素晶型由纤维素Ⅰ型转化为纤维素Ⅱ型;回收后的离子液体结构没发生变化,重复利用仍保持较好的溶解微晶纤维素的能力.

  11. Enzymatic hydrolysis of microcrystalline cellulose and pretreated wheat straw: a detailed comparison using convenient kinetic analysis.

    Science.gov (United States)

    Monschein, Mareike; Reisinger, Christoph; Nidetzky, Bernd

    2013-01-01

    Marked slow-down of soluble sugar production at low degree of substrate conversion limits the space-time yield of enzymatic hydrolysis of ligno-cellulosic materials. A simple set of kinetic descriptors was developed to compare reducing sugar release from pure crystalline cellulose (Avicel) and pretreated wheat straw by Trichoderma reesei cellulase at 50 °C. The focus was on the rate-retarding effect of maximum hydrolysis rate at reaction start (r(max)), limiting hydrolysis rate (r(lim)) at extended reaction time (24h), and substrate conversion, marking the transition between the r(max) and r(lim) kinetic regimes (C(trans)). At apparent saturation of substrate (12.2g cellulose/L) with enzyme, r(max) for pretreated wheat straw (~9.6g/L/h) surpassed that for Avicel by about 1.7-fold whereas their r(lim) were almost identical (~0.15 g/L/h). C(trans) roughly doubled as enzyme/substrate loading was increased from 3.8 to 75FPU/g, suggesting C(trans) to be a complex manifestation of cellulase-cellulose interaction, not an intrinsic substrate property. A low-temperature adsorption step preceding hydrolysis at 50 °C resulted in enhanced cellulase binding at reaction start without increasing r(max). C(trans) was higher for pretreated wheat straw (~30%) than for Avicel (~20%) under these conditions. Copyright © 2012 Elsevier Ltd. All rights reserved.

  12. Chitosan-kaolin coprecipitate as disintegrant in microcrystalline cellulose-based pellets elaborated by extrusion-spheronization.

    Science.gov (United States)

    Goyanes, Alvaro; Souto, Consuelo; Martínez-Pacheco, Ramón

    2013-02-01

    The usefulness of a coprecipitate of chitosan and kaolin as disintegrant in the pellets of microcrystalline cellulose (MCC) and hydrochlorothiazide (HCT) (as a model of poorly water-soluble drug) produced by extrusion-spheronization was evaluated in this study. The effectiveness of chitosan-kaolin coprecipitate to increase the dissolution rate was compared with that of kaolin and chitosan. A possible synergy effect was also evaluated between the coprecipitate, kaolin or chitosan and sorbitol, added to the pellets as a very water-soluble diluent. The chitosan-kaolin coprecipitate, the kaolin or the chitosan allowed pellets to be obtained of adequate size, roundness, mechanical strength and flow properties. Furthermore, the incorporation of chitosan-kaolin coprecipitate or chitosan significantly increased the dissolution rate of HCT independently of the sorbitol content. The effects on the dissolution of HCT derived from the incorporation of coprecipitate to the pellets can be attributed to its content of chitosan. However, the addition of kaolin into the pellets did not significantly affect the HCT dissolution process. The pellets incorporating coprecipitated chitosan-kaolin or chitosan and the maximum proportion of sorbitol (50%) led to the highest HCT dissolution rate and experienced a rapid and complete disintegration in the dissolution medium.

  13. Preparation of zeolite covered cellulose fibers

    Energy Technology Data Exchange (ETDEWEB)

    Mintova, S.; Valtchev, V. [Institute of Applied Mineralogy, Sofia (Bulgaria)

    1995-12-01

    Membrane separation has proved to be an important technology in chemical industry. That is why the design of different type of zeolite containing membranes has received much attention during the last decade. Zeolite containing filters and membranes were prepared by embedding zeolite crystals with adhesive substances in the cellulose matrix. This communication discussed the preparation of zeolite containing cellulose materials by in situ crystallization. Discussed axe: (1) the effect of the vegetal fiber structure and chemical composition (2) the effect of the type of the zeolite coating; (3) the effect of the mechanical and chemical treatment of the fibers on the process of the fiber zeolite coating.

  14. PREPARATION AND CHARACTERIZATION OF BAMBOO NANOCRYSTALLINE CELLULOSE

    Directory of Open Access Journals (Sweden)

    Mengjiao Yu,

    2012-02-01

    Full Text Available Nanocrystalline cellulose (NCC has many potential applications because of its special properties. In this paper, NCC was prepared from bamboo pulp. Bamboo pulp was first pretreated with sodium hydroxide, followed by hydrolysis with sulfuric acid. The concentration of sulfuric acid and the hydrolysis time on the yield of NCC were studied. The results showed that sulfuric acid concentration had larger influence than the hydrolysis time on the yield of NCC. When the temperature was 50oC, the concentration of sulfuric acid was 48wt% and the reaction time was 30 minutes, a high quality of nanocrystalline cellulose was obtained; under these conditions, the length of the nanocrystalline cellulose ranged from 200 nm to 500 nm, the diameter was less than 20 nm, the yield was 15.67wt%, and the crystallinity was 71.98%, which is not only higher than those of cellulose nanocrystals prepared from some non-wood materials, but also higher than bamboo cellulose nanocrystals prepared by other methods.

  15. Preparation of hydrogenated microcrystalline silicon films with hot-wire-assisted MWECR-CVD system

    Institute of Scientific and Technical Information of China (English)

    He Bin; Chen Guang-Hua; Zhu Xiu-Hong; Zhang Wen-Li; Ding Yi; Ma Zhan-Jie; Gao Zhi-Hua; Song Xue-Mei; Deng Jin-Xiang

    2006-01-01

    Intrinsic hydrogenated microcrystalline silicon (μc-Si:H) films have been prepared by hot-wire-assisted microwave electron-cyclotron-resonance chemical vapour deposition (Hw-MwECR-CVD) under different deposition conditions.Fourier-transform infrared spectra and Raman spectra were measured.Optical band gap WaS determined by Tauc plots,and experiments of photo-induced degradation were performed.It was observed that hydrogen dilution plays a more essential role than substrate temperature in microcrystalline transformation at low temperatures. Crystalline volume fraction and mean grain size in the films increase with the dilution ratio (R=H2/(H2+SiH4)).With the rise of crystallinity in the films,the optical band gap tends to become narrower while the hydrogen content and photo-induced degradation decrease dramatically.The samples,were identified as μc-Si:H films,by calculating the optical band gap.It is considered that hydrogen dilution has an effect on reducing the crystallization activation energy of the material,which promotes the heterogeneous solid-state phase transition characterized by the Johnson-Mehl-Avrami (JMA) equation.The films with the needed structure can be prepared by balancing deposition and crystaUization through controlling process parameters.

  16. 微晶纤维素在离子液体[Bmim]Cl中的溶解与再生%Dissolution and regeneration of microcrystalline cellulose in ionic liquid [Bmim]Cl

    Institute of Scientific and Technical Information of China (English)

    邹鑫; 杨继涛; 胡国新

    2013-01-01

    利用氯化1-丁基-3-甲基咪唑([Bmim]Cl)溶解微晶纤维素,考察了温度、时间以及[Bmim]Cl与微晶纤维素质量比对微晶纤维素在[Bmim]Cl中的溶解率的影响.研究结果表明,[Bmim]Cl与微晶纤维素质量比为5∶0.5,溶解温度为90℃,溶解时间为1.5 h时,微晶纤维素在[Bmim]Cl中的溶解率最高,为48.7%.同时,借助扫描电镜和X射线衍射仪对再生纤维素的形貌和结晶性进行了分析,结果表明,微晶纤维素在[Bmim]Cl中的溶解属于直接溶解,结晶强度减弱.%1-Butyl-3-methylimidazolium chloride ([Bmim]Cl) was used to dissolve microcrystalline cellulose.Temperature,time and mass ratio of [Bmim]Cl and microcrystalline cellulose which had influence on the dissolving rate of microcrystalline cellulose were investigated.The results showed that the highest dissolving rate of microcrystalline cellulose in [Bmim]Cl achieved 48.7% when the mass ratio of [Bmim]Cl and microcrystalline cellulose was 5:0.5,solution temperature was 90 ℃,lysis time was 1.5 h.The appearance and crystallinity of regenerated cellulose were analyzed by using scanning electron microscope and X-ray diffraction.The results showed that the dissolution of microcrystalline cellulose in [Bmim]Cl was a physical process,and the regenerated cellulose exhibited declining of the crystallization intensity.

  17. A novel cellulose hydrogel prepared from its ionic liquid solution

    Institute of Scientific and Technical Information of China (English)

    LI Lu; LIN ZhangBi; YANG Xiao; WAN ZhenZhen; CUI ShuXun

    2009-01-01

    A novel cellulose hydrogel is prepared by regenerating cellulose from its ionic liquid solution. The transparency cellulose hydrogel presents a good chemical stability and an acceptable mechanical property. This non-toxic cellulose hydrogel should be biocompatibie and may be useful in the future as a biomaterial.

  18. Microcrystalline B-doped window layers prepared near amorphous to microcrystalline transition by HWCVD and its application in amorphous silicon solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, P. [Department of Physics/Center of Optical Technologies and Laser Controlled Processes, University of Kaiserslautern, P.O. Box 3049, Kaiserslautern D-67653 (Germany)]. E-mail: kumarp@rhrk.uni-kl.de; Kupich, M. [Department of Physics/Center of Optical Technologies and Laser Controlled Processes, University of Kaiserslautern, P.O. Box 3049, Kaiserslautern D-67653 (Germany); Grunsky, D. [Department of Physics/Center of Optical Technologies and Laser Controlled Processes, University of Kaiserslautern, P.O. Box 3049, Kaiserslautern D-67653 (Germany); Schroeder, B. [Department of Physics/Center of Optical Technologies and Laser Controlled Processes, University of Kaiserslautern, P.O. Box 3049, Kaiserslautern D-67653 (Germany)

    2006-04-20

    The electronic and structural properties of p-type microcrystalline silicon films prepared near the microcrystalline to amorphous ({mu}c-amorphous) transition by hot-wire chemical vapor deposition are studied. Silane is used as a source gas while H{sub 2} as diluent and trimethylboron (TMB) and boron trifluoride (BF{sub 3}) as doping gases. Increasing TMB concentration from 0.01% to 5% favors the amorphous growth whereas for BF{sub 3} the crystalline fraction remains constant. The dark conductivity ({sigma} {sub d}) of {mu}c-Si:H p-layers remains approximately constant for TMB 1-5% at constant crystalline fraction X {sub c}. This dark conductivity behavior is attributed to the decrease in doping efficiency with increasing TMB concentration. The best initial efficiency obtained for a 400 nm amorphous pin solar cell with optimized {mu}c-Si:H p-layer is 7.7% (V {sub oc} = 874 mV, J {sub sc} = 12.91 mA/cm{sup 2}, FF = 68%)

  19. Preparation and characterization agar-based nanocomposite film reinforced by nanocrystalline cellulose.

    Science.gov (United States)

    Atef, Maryam; Rezaei, Masoud; Behrooz, Rabi

    2014-09-01

    Nanocrystalline cellulose (NCC) was prepared from microcrystalline cellulose (MCC) with particle size of 24.7 μm using sulfuric acid hydrolysis technique. The obtained NCC revealed size of 0-100 nm, which the major part of them was about 30 nm. Then different contents (2.5, 5 and 10 wt%) of these NCC incorporated in agar film solution and the morphology, structure, and properties of the nanocomposite films were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier transforms infrared (FTIR) spectroscopy, differential scanning calorimetry (DSC), mechanical, physical and optical testing. Results showed that the water vapor permeability (WVP) and water solubility (WS) of the agar-based nanocomposite films significantly (P0.05). In addition, swelling percentage, transparency and light transmission of the films were decreased by incorporating NCC into polymer matrix.

  20. Preparation and characterization of nanocrystal cellulose%纳米纤维素的制备与表征

    Institute of Scientific and Technical Information of China (English)

    刘慧芳; 毛海龙; 王战勇

    2015-01-01

    Nanocrystal cellulose was prepared by sulfuric acid hydrolysis microcrystalline cellulose .The optimal conditions for the preparation of nanocrystal cellulose were chosen as follows :sulfuric acid initial concentration is 35%,reaction temperature is 40℃,and reaction time is 90 min.Under this condition ,the yield of nanocrystal cellulose reached 83.55%.The morphological structure of the product is verified to be nano-scale by SEM and TEM .Crystallinity of nanocrystal cellulose is higher than that of nanocrystal cellulose according to the results of XRD .The analysis of thermo gravimetric shows the thermal stability of nanocrystal cellulose is worse than microcrystalline cellulose .%以微晶纤维素为原料,通过硫酸酸解制备获得了纳米纤维素。实验优选获得了酸解制备纳米纤维素的优化条件为:硫酸初始浓度35%,反应温度40℃,酸解时间90 min,此优化条件下,纳米纤维素的产率可达83.55%;SEM和TEM观察产物的形态外貌,确定为纳米级纤维素;XRD分析显示纳米纤维素的结晶度要高于微晶纤维素,而TG分析显示NCC的热稳定性要低于微晶纤维素。

  1. Use of cellobiohydrolase-free cellulase blends for the hydrolysis of microcrystalline cellulose and sugarcane bagasse pretreated by either ball milling or ionic liquid [Emim][Ac].

    Science.gov (United States)

    Teixeira, Ricardo Sposina Sobral; da Silva, Ayla Sant'Ana; Kim, Han-Woo; Ishikawa, Kazuhiko; Endo, Takashi; Lee, Seung-Hwan; Bon, Elba P S

    2013-12-01

    This study investigated the requirement of cellobiohydrolases (CBH) for saccharification of microcrystalline cellulose and sugarcane bagasse pretreated either by ball milling (BM) or by ionic liquid (IL) [Emim][Ac]. Hydrolysis was done using CBH-free blends of Pyrococcus horikoshii endoglucanase (EG) plus Pyrococcus furiosus β-glucosidase (EGPh/BGPf) or Optimash™ BG while Acremonium Cellulase was used as control. IL-pretreated substrates were hydrolyzed more effectively by CBH-free enzymes than were the BM-pretreated substrates. IL-treatment decreased the crystallinity and increased the specific surface area (SSA), whereas BM-treatment decreased the crystallinity without increasing the SSA. The hydrolysis of IL-treated cellulose by EGPh/BGPf showed a saccharification rate of 3.92 g/Lh and a glucose yield of 81% within 9h. These results indicate the efficiency of CBH-free enzymes for the hydrolysis of IL-treated substrates. Copyright © 2013 Elsevier Ltd. All rights reserved.

  2. Activation of Microcrystalline Cellulose by Two-step Method and Its Use in Immobilization of Papain%两步法活化微晶纤维素及在固定木瓜蛋白酶中的应用

    Institute of Scientific and Technical Information of China (English)

    郭刚军; 马林; 谢文林; 陈国雄; 古练权

    2001-01-01

    Immobilized papain was prepared using microcrystalline cellulos as support which was activated by two-step method.The microcrystalline cellulose was first activated with p-toluenesulfonyl chloride, followed by coupling with ethyl diamine.After treated with glutaraldehyde, papain was immobilized to the support.Immobilized papain was obtained with activity 103 U/g support and high stability.%微晶纤维素经过两步活化,可在温和条件下实现木瓜蛋白酶固定化.用对甲基苯磺酰氯活化微晶纤维素后,与乙二胺反应向载体引入有机胺基团,再用戊二醒处理所得的二次活化载体可在温和条件固定木瓜蛋白酶.所得固定化酶活力为103 U/g载体,与溶液酶比较,热稳定性有明显提高.

  3. Preparation of carboxymethyl cellulose produced from purun tikus (Eleocharis dulcis)

    Science.gov (United States)

    Sunardi, Febriani, Nina Mutia; Junaidi, Ahmad Budi

    2017-08-01

    Sodium carboxymethyl cellulose (Na-CMC) is one of the important modified cellulose, a water-soluble cellulose, which is widely used in many application of food, pharmaceuticals, detergent, paper coating, dispersing agent, and others. The main raw material of modified cellulose is cellulose from wood and cotton. Recently, much attention has been attracted to the use of various agriculture product and by-product, grass, and residual biomass as cellulose and modified cellulose source for addressing an environmental and economic concern. Eleocharis dulcis, commonly known as purun tikus (in Indonesia), is a native aquatic plant of swamp area (wetland) in Kalimantan, which consists of 30-40% cellulose. It is significantly considered as one of the alternative resources for cellulose. The aims of present study were to isolate cellulose from E. dulcis and then to synthesise Na-CMC from isolated cellulose. Preparation of carboxymethyl cellulose from E. dulcis was carried out by an alkalization and etherification process of isolated cellulose, using various concentration of sodium hydroxide (NaOH) and monochloroacetic acid (MCA). The results indicated that the optimum reaction of alkalization was reached at 20% NaOH and etherification at the mass fraction ratio of MCA to cellulose 1.0. The optimum reaction has the highest solubility and degree of substitution. The carboxymethylation process of cellulose was confirmed by Fourier Transform Infrared spectroscopy (FTIR). In addition, changes in crystallinity of cellulose and Na-CMC were evaluated by X-ray diffraction (XRD).

  4. Preparation and Characterization of Jute Cellulose Crystals-Reinforced Poly(L-lactic acid Biocomposite for Biomedical Applications

    Directory of Open Access Journals (Sweden)

    Mohammed Mizanur Rahman

    2014-01-01

    Full Text Available Crystalline cellulose was extracted from jute by hydrolysis with 40% H2SO4 to get mixture of micro/nanocrystals. Scanning electron microscope (SEM showed the microcrystalline structure of cellulose and XRD indicated the Iβ polymorph of cellulose. Biodegradable composites were prepared using crystalline cellulose (CC of jute as the reinforcement (3–15% and poly(lactic acid (PLA as a matrix by extrusion and hot press method. CC was cellulose derived from mercerized and bleached jute fiber by acid hydrolysis to remove the amorphous regions. FT-IR studies showed hydrogen bonding between the CC and the PLA matrix. The X-ray diffraction (XRD and differential scanning calorimetry (DSC studies showed that the percentage crystallinity of PLA in composites was found to be higher than that of neat PLA as a result of the nucleating ability of the crystalline cellulose. Furthermore, Vicker hardness and yield strength were found to increase with increasing cellulose content in the composite. The SEM images of the fracture surfaces of the composites were indicative of poor adhesion between the CC and the PLA matrix. The composite with 15% CC showed antibacterial effect though pure films but had no antimicrobial effect; on the other hand its cytotoxicity in biological medium was found to be medium which might be suitable for its potential biomedical applications.

  5. Comparison of γ-irradiation with other pretreatments followed with simultaneous saccharification and fermentation on bioconversion of microcrystalline cellulose for bioethanol production.

    Science.gov (United States)

    Liu, Yun; Zhou, Hua; Wang, Shihui; Wang, Keqin; Su, Xiaojun

    2015-04-01

    The effect of γ-irradiation pretreatment was compared with other pretreatment methods including ionic liquids (ILs), 1% HCl, 1% H2SO4, acidic aqueous Ils (AA-ILs), on the bioconversion efficiency of microcrystalline cellulose (MCC) for bioethanol production. The efficiency of MCC pretreatment followed with simultaneous saccharification and fermentation (SSF) was firstly evaluated according to the variations of the irradiation-derived compounds and structure of MCC, as well as yeast growth curve and bioethanol yield. Results showed that the appropriate irradiation dose (891 kGy used in our work) could eliminate the negative effect of toxic irradiation-derived compounds on SSF for ethanol bioconversion with the yield value of 67%. Analyses of SEM, FT-IR, reducing sugar and bioethanol yield showed that the efficiency of pretreatment on MCC was ILs ≈ irradiation pretreatment > AA-ILs pretreatment > 1% HCl pretreatment > 1% H2SO4 pretreatment.

  6. Performance Study about Film of Mercerizing Reguar and Microcrystalline Cellulose in the Ionic Liquids%丝瓜络和微晶纤维素在离子液体中成膜性能研究

    Institute of Scientific and Technical Information of China (English)

    陈梅; 魏莉; 王迎; 赵吉祥

    2011-01-01

    [ Objective] The aim was to study performance about film of mercerizing reguar and mierocrystalline cellulose in the ionic liquids. [Method] Regenerated cellulose film was prepared from mercerizing reguar in 1-butyl, 3-methylimidazolium chloride ionic liquid. Properties and structures of the mercerizing reguar and obtained regenerated cellulose films were investigated by FTIR and polarized light microscopy, then contrasted by microcrystalline cellulose. At last, the performance of film was evaluatied. [Result] The results showed that, 1-butyl, 3-methylimidazolium chloride ionic liquid was good non-derivatizing solvents for mercerizing reguar. Mercerizing reguar and mierocrystalline cellulose were compared, it found that dissolve time and solubility in ionic liquids were serious influenced by the degree of polymerization. [ Conclusion] Cellulose film had a certain hole rate and aperture, could be used in permeation and separation field.%[目的]研究丝瓜络和微晶纤维素在离子液体中成膜性能.[方法]以离子液体[BMIM]Cl为溶剂溶解预处理过的丝瓜络,制得纤维素膜,用红外光谱和偏光显微镜对溶解前后的丝瓜络纤维进行表征,并对纤维素膜作了基本的性能评价.[结果]与微晶纤维素为原料的对比试验表明,[BMIM]Cl是丝瓜络纤维的直接溶剂,溶解过程中没有衍生物生成.原料聚合度的大小严重影响纤维素在离子液体中的溶解时间和溶解度.[结论]制备的纤维素平板膜具备一定的空隙率和孔径,可广泛应用于渗透、分离等领域.

  7. Size- and dose-dependent toxicity of cellulose nanocrystals (CNC) on human fibroblasts and colon adenocarcinoma.

    Science.gov (United States)

    Hanif, Zahid; Ahmed, Farrukh R; Shin, Seung Won; Kim, Young-Kee; Um, Soong Ho

    2014-07-01

    A controlled preparation of cellulose nanocrystals of different sizes and shapes has been carried out by acid hydrolysis of microcrystalline cellulose. The size- and concentration-dependent toxicity effects of the resulting cellulose nanocrystals were evaluated against two different cell lines, NIH3T3 murine embryo fibroblasts and HCT116 colon adenocarcinoma. It could serve as a therapeutic platform for cancer treatment.

  8. Combined effects of raw materials and solvent systems on the preparation and properties of regenerated cellulose fibers.

    Science.gov (United States)

    Chen, Jinghuan; Guan, Ying; Wang, Kun; Zhang, Xueming; Xu, Feng; Sun, Runcang

    2015-09-05

    To investigate the combined effects of materials and solvents on the preparation, structural and mechanical properties of regenerated cellulose fibers, four cellulosic materials (microcrystalline cellulose, cotton linter pulp, bamboo pulp and bleached softwood sulfite dissolving pulp) and six non-derivative solvents (NaOH/urea aqueous solution, N,N-dimethylacetamide/lithium chloride, N-methyl-morpholine-N-oxide, 1-butyl-3-methylimidazolium chloride, 1-allyl-3-methylimidazolium chloride and 1-ethyl-3-methylimidazolium acetate) were used to prepare fibers with wet spinning method. The results showed that the dissolvability of solvent was the determining factor in cellulose dissolution, and the dissolving time was influenced by the raw materials' properties, such as molecular weight, exposed area and hemicellulose content. The crystallinity and elongation at break of the fibers were almost fixed and not affected by the materials and solvents. However, the tensile strength of the fibers was directly proportional to the molecular weight of the raw materials, and varied with the type of solvents through cellulose degradation.

  9. Preparation and Characterization of Super Absorbent Resin from Natural Cellulose

    Institute of Scientific and Technical Information of China (English)

    李杰; 马凤国; 谭惠民

    2003-01-01

    The grafting polyacrylamide onto wood pulp cellulose (cell-g-PAM) was performed with cerous ammonium nitrate as the initiator and hydrolyzed to produce the super absorbent resin. The FTIR shows that the polyacrylamide is grafted on the cellulose. After hydrolyzation, part of acrylamino groups are transformed into carboxyl groups. The XRD analysis shows that the graft polymerization occurred at the amorphous section and the surface of the crystal section of cellulose. The SEM graph reveals that there is a layer of polymer on the surface of cellulose fiber and the fibril structure of the cellulose surface is covered. After hydrolyzation, the surface of the product is different from that of cell-g-PAM's and the surface is scraggy. The technical conditions to prepare high water absorbent resin were confirmed. Through the radical graft copolymerization, the high water absorbent resin can be produced from wood pulp cellulose.

  10. Preparation of cellulose from corncobs I: Study on cellulose extraction

    Directory of Open Access Journals (Sweden)

    Pongnoree, J.

    2006-01-01

    Full Text Available The extraction of fat from corncob powder was determined using hexane and 95% ethanol solution for 4, 8 and 12 hrs. The selected powder was subjected to protein separation using 10, 15 and 20% NaOH for 15, 30 and 45 min. The obtained product was then bleached using 10, 15 and 20% H2O2 for 1.5, 3.0 and 4.5 hrs. It was found that the suitable condition for fat extraction was using 95% ethanol for 8 hrs. The optimal condition for protein extraction was using 15% NaOH for 30 min. and the bleaching condition was using 10% H2O2 for 1.5 hrs. The obtained product contained 76.90% cellulose (dry basis and the chemical composition and physical properties were also determined.

  11. Preparation and physical properties of tara gum film reinforced with cellulose nanocrystals.

    Science.gov (United States)

    Ma, Qianyun; Hu, Dongying; Wang, Lijuan

    2016-05-01

    Cellulose nanocrystals (CNC) prepared from microcrystalline cellulose were blended in tara gum solution to prepare nanocomposite films. The morphology, crystallinity, and thermal properties of the CNC and films were evaluated by using transmission electron microscopy, X-ray diffractometry, and thermogravimetric analysis, respectively. The resultant CNC was rod-shaped with diameters of around 8.6 nm. The effect of CNC content on physical and thermal properties of films was studied. The composite film tensile strength increased from 27.86 to 65.73 MPa, elastic modulus increased from 160.98 MPa to 882.49 MPa and the contact angle increased from 55.8° to 98.7° with increasing CNC content from 0 to 6 wt%. However, CNC addition increased the thermal stability slightly and CNC content above 6 wt% decreased the tensile strength by CNC aggregation in the matrix. The nanocomposite film containing 6 wt% CNC possessed the highest light transmittance, mechanical properties, and lowest oxygen permeability. CNC addition is a suitable method to modify tara gum matrix polymer properties.

  12. The effect of microcrystalline cellulose crystallinity on the hydrophilic property of tablets and the hydrolysis of acetylsalicylic acid as active pharmaceutical ingredient inside tablets.

    Science.gov (United States)

    Awa, Kimie; Shinzawa, Hideyuki; Ozaki, Yukihiro

    2015-08-01

    The crystal structures of active pharmaceutical ingredients and excipients should be strictly controlled because they influence pharmaceutical properties of products which cause the change in the quality or the bioavailability of the products. In this study, we investigated the effects of microcrystalline cellulose (MCC) crystallinity on the hydrophilic properties of tablets and the hydrolysis of active pharmaceutical ingredient, acetylsalicylic acid (ASA), inside tablets by using tablets containing 20% MCC as an excipient. Different levels of grinding were applied to MCC prior to tablet formulation, to intentionally cause structural variation in the MCC. The water penetration and moisture absorbability of the tablets increased with decreasing the crystallinity of MCC through higher level of grinding. More importantly, the hydrolysis of ASA inside tablets was also accelerated. These results indicate that the crystallinity of MCC has crucial effects on the pharmaceutical properties of tablets even when the tablets contain a relatively small amount of MCC. Therefore, controlling the crystal structure of excipients is important for controlling product qualities.

  13. Ultrasound-assisted ionic liquid-based micellar extraction combined with microcrystalline cellulose as sorbent in dispersive microextraction for the determination of phenolic compounds in propolis.

    Science.gov (United States)

    Cao, Jun; Peng, Li-Qing; Du, Li-Jing; Zhang, Qi-Dong; Xu, Jing-Jing

    2017-04-22

    An ionic liquid-(IL) based micellar extraction combined with microcrystalline cellulose- (MCC) assisted dispersive micro solid-phase extraction method was developed to extract phenolic compounds from propolis. A total of 20 target compounds were identified by ultra-high- performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry. The main extraction parameters were optimized and included the ultrasonic power, ultrasonic time, sample pH, type of IL, the concentration of [C12mim]Br, extraction time, concentration of MCC, type of sorbent and type of elution solvents. Under the optimum conditions, the proposed method exhibited good linearities (r(2) ≥ 0.999) for all plant phenolic compounds with the lower limits of detection in the range of 0.21-0.41 ng/mL. The recoveries ranged from 82.74% to 97.88% for pinocembrin, chrysin and galangin. Compared with conventional solvent extraction, the present method was simpler and more efficient and required less organic solvent and a shorter extraction time. Finally, the methodology was successfully used for the extraction and enrichment of phenolic compounds in propolis. Copyright © 2017 Elsevier B.V. All rights reserved.

  14. Microcrystalline cellulose, a useful alternative for sucrose as a matrix former during freeze-drying of drug nanosuspensions - a case study with itraconazole.

    Science.gov (United States)

    Van Eerdenbrugh, Bernard; Vercruysse, Sofie; Martens, Johan A; Vermant, Jan; Froyen, Ludo; Van Humbeeck, Jan; Van den Mooter, Guy; Augustijns, Patrick

    2008-10-01

    Itraconazole nanosuspensions, stabilized with 10% TPGS (relative to the weight of itraconazole), were transformed into nanoparticulate powders by freeze-drying. The crystalline itraconazole nanoparticles showed peak broadening in the X-ray powder diffraction spectra and a lower melting point as inferred from differential scanning calorimetry. As it was found that freeze-drying compromised dissolution behavior, sucrose was added as a matrix, former (50,100 and 200%, relative to the weight of itraconazole). Higher amounts of sucrose unexpectedly resulted in a decrease in the dissolution rate. After thorough evaluation of the powders, it was found that whereas higher sucrose content showed a cryoprotective effect, agglomeration during the final phase of the subsequent drying step tended to increase with higher amounts of sucrose. Therefore, microcrystalline cellulose (MCC) was evaluated as an alternative matrix former. The inclusion of MCC resulted in fast dissolution that increased with increasing amounts of MCC [for powders containing 50%,100% and 200% MCC, (relative to the weight of itraconazole), the times required for 63.2% release were 10.5+/-0.7, 6.4+/-1.2 and 3.1+/-0.5min, respectively]. The dissolution profiles showed an initial phase of burst dissolution, followed by a phase of slower release. As the fraction showing burst dissolution increased with higher MCC content, the system holds promise to maintain the dissolution enhancing properties of nanoparticles in the dry form.

  15. Preparation and characterization of gelatin scaffold containing microorganism fermented cellulose

    Energy Technology Data Exchange (ETDEWEB)

    Lim, Youn Mook; Gwon, Hui Jeong; Park, Jong Seok; Nho, Young Chang; Lee, Byeong Heon [Korea Atomic Energy Research Institute, Jeongeup (Korea, Republic of); Kim, Mi Yeong; Lee, Jong Dae; Song, Sung Gi [Quegenbiotech, Co., Incheon (Korea, Republic of)

    2010-12-15

    Cellulose, chitin, chitosan and hyaluronic acid are well known as polysaccharides. These polysaccharides have many effects on cell growth and differentiation. Cell activation increases with increasing the polysaccharides concentration. In this study, gelatin scaffold containing microorganism fermented cellulose, citrus gel were prepared by using irradiation technique. Physical properties of the scaffolds were investigated as a function of the concentrations of gelatin and citrus gel and the cell attachment, cell morphology and inflammation of the scaffolds also were characterized for regeneration of skin tissue.

  16. A técnica da reflectância difusa aplicada ao estudo da fluorescência de 2,3-naftalimidas n-substituídas com grupos alquila incluídas em b-ciclodextrina e adsorvidas em celulose microcristalina Diffuse reflectance technique applied to a fluorescence study of n-alkyl substituted 2,3-naphthalimides included in b-ciclodextrin and adsorbed in microcrystalline cellulose

    Directory of Open Access Journals (Sweden)

    Luis Filipe Vieira Ferreira

    1999-07-01

    Full Text Available The solution fluorescence of N-alkyl-2,3-naphthalimides (1-4 in polar protic and aprotic solvents was compared to the emission from solid samples resulting from the imide complexation with b-cyclodextrin or adsorption on the surface of microcrystalline cellulose. Solid samples of the inclusion complex 2,3-naphthalimides/b-cyclodextrin show maximum for fluorescence emission significantly different to the observed in methanolic solution. Beside this, a clear effect on the alkyl chain length could be observed for these samples which is probably due to differences in probe location inside the cyclodextrin cavity. The constancy for fluorescence quantum yield and fluorescence lifetime for the imides 1 - 4 adsorbed on microcrystalline cellulose suggests that, independently of the polarity of the solvent used for sample preparation, the probe is preferentially located on the cellulose surface. An increase of fluorescence quantum yield and fluorescence lifetime for solid samples, when compared to the values obtained in solution for the different solvents employed in this study (acetonitrile, methanol and water, is fully in accordance with a decrease of the probe mobility due to inclusion in b-cyclodextrin or to adsorption on cellulose.

  17. Influence of total gas flow rate on microcrystalline silicon films prepared by VHF-PECVD

    Institute of Scientific and Technical Information of China (English)

    Gao Yan-Tao; Zhang Xiao-Dan; Zhao Ying; Sun Jian; Zhu Feng; Wei Chang-Chun; Chen Fei

    2006-01-01

    Hydrogenated microcrystalline silicon (μc-Si:H) films are fabricated by very high frequency plasma enhanced chemical vapour deposition (VHF-PECVD) at a silane concentration of 7% and a varying total gas flow rate (H2+SiH4).Relations between the total gas flow rate and the electrical and structural properties as well as deposition rate of the films are studied. The results indicate that with the total gas flow rate increasing the photosensitivity and deposition rate increase, but the crystalline volume fraction (Xc) and dark conductivity decrease. And the intensity of (220) peak first increases then decreases with the increase of the total gas flow rate. The cause for the changes in the structure and deposition rate of the films with the total gas flow rate is investigated using optical emission spectroscopy (OES).

  18. High Yield Preparation Method of Thermally Stable Cellulose Nanofibers

    Directory of Open Access Journals (Sweden)

    Hongli Zhu

    2014-02-01

    Full Text Available The preparation of nanocellulose fibers (NFs is achieved through pretreating cellulose in a NaOH/urea/thiourea solution, and then defibrillating the fibers through ultrasonication, resulting in a high yield of 85.4%. Extensive work has been done to optimize the preparation parameters. The obtained NFs are about 30 nm in diameter with cellulose II crystal structure. They possess high thermal stability with an onset of thermal degradation at 270 °C and a maximum degradation temperature of 370 °C. Such NFs have potential applications in transistors and batteries with high thermal stability. NFs-H were obtained by homogenizing undefibrillated fibers separated from the preparation of NFs. NFs-H were also in cellulose II crystal form but with lower thermal stability due to low crystallinity. They can be applied to make highly transparent paper.

  19. [Tableting technology of a dry extract from Solidago virgaurea L. with the use of silicified microcrystalline cellulose (Prosolv) and other selected auxiliary substances].

    Science.gov (United States)

    Marczyiński, Zbigniew

    2009-01-01

    Direct tableting is simpler and more cost-effective from the point of view of good manufacturing practice (GMP) than wet granulation or dry compacting. Moreover, the use of dry plant extracts in the process of direct tableting, omitting granulation, decreases the possibility of biological activity loss of active substances. Thus, pharmaceutical industry uses this particular process more and more frequently. Only few therapeutic substances form under compression tablets meeting current requirements. Very often addition of auxiliary substances appears to be indispensable. The aim of this study was to obtain uncoated tablets by the method of direct tableting with the use of selected auxiliary substances. Dry extract from Solidago virgaurea L. was the study material. Shrimp chitosan, silicified microcrystalline cellulose (Prosolv), polyvinylpyrrolidone, calcium carbonate and sodium stearyl fumarate were used as auxiliary substances. Eleven tablet batches were manufactured in a reciprocating instrumented tableting machine (Ewreka). The produced tablets were subjected to morphological tests comprising the tablet size, determination of batching accuracy (determination of mass uniformity of individual tablets), test of mechanical resistance (crushing strength), determination of disintegration time. The statistical hardness of the manufactured tablets was also estimated. Pharmaceutical availability tests were performed of the biologically active substances released from tablets to the acceptor fluid. The study was based on general and detailed regulations of Polish Pharmacopoeia VII (PP VII). The obtained results allow to conclude that the applied auxiliary substances appeared to be useful in adequate proportions in manufacturing tablets containing dry extract from Solidago virgaurea L. The properties of the obtained batches of tablets were in majority consistent with the current requirements. The applied method provides technological reproducibility and high durability of

  20. Conformation of Sodium Microcrystalline Cellulose Sulfate in Aqueous Solution%微晶纤维素硫酸钠溶液的构象

    Institute of Scientific and Technical Information of China (English)

    李琳; 熊文雯; 王兆梅

    2006-01-01

    Sodium microcrystalline cellulose sulfate ( NaCSMC) is a new type of effective anti-coagulant, whose anti-coagulant activity is closely related to the conformation in solution. In order to reveal the anti-coagulant activity of NaCSMC, the conformation of NaCSMC in aqueous solution was investigated by the optical rotation measurement, the viscosity analysis and the Congo red helix-coil transition analysis. The measurement results of optical rotation show that the conformation of NaCSMC is regular in neutral or weak alkaline solution. The same results can also be obtained by means of viscosity analysis. Moreover, it is indicated by the Congo red helix-coil transition analysis that the conformation of NaCSMC in aqueous solution is of not only regular conformation but also single helix and multi-helix structures.%微晶纤维素硫酸钠是一种具有显著抗凝血活性的物质,其抗凝活性与其在溶液中的构象密切相关.为了解其抗凝活性,文中通过旋光度分析、粘度分析和刚果红螺旋-线团过渡分析,研究了微晶纤维素硫酸钠溶液的构象.旋光度分析表明,微晶纤维素硫酸钠在水溶液或弱碱溶液中具有规则的空间构象;由粘度分析也可得出同样的结果;刚果红螺旋-线团过渡分析表明,微晶纤维素硫酸钠在溶液中具有规则的空间构象,同时具有单螺旋结构与高级螺旋结构.

  1. Characterization of microcrystalline I-layer for solar cells prepared in low temperature - plastic compatible process

    KAUST Repository

    Sliz, Rafal

    2012-06-01

    Microcrystalline silicon (mc-Si) lms deposited using a Plasma Enhanced Chemical Vapour Deposition (PECVD) process constitute an important material for manufacturing low-cost, large-area thin-lm devices, such as solar cells or thin-lm transistors. Although the deposition of electronic-grade mc-Si using the PECVD process is now well established, the high substrate temperature required (~400°C) does not lend itself to electronic devices with exible form factors fabricated on low-cost plastic substrates. In this study, we rst investigated an intrinsic mc-Si layer deposited at plastic-compatible substrate temperatures (~150°C) by characterising the properties of the lm and then evaluated its applicability to p-i-n solar cells though device characterisation. When the performance of the solar cell was correlated with lm properties, it was found that, although it compared unfavourably with mc-Si deposited at higher temperatures, it remained a very promising option. Nonetheless, further development is required to increase the overall eciency of mc-Si exible solar cells.

  2. Characteristics of microcrystalline cellulose and its application in neutral dairy beverage%微晶纤维素特性及其在中性乳饮料中的应用研究

    Institute of Scientific and Technical Information of China (English)

    薛玉清; 舒成亮; 余立意; 杨忻怡; 欧凯; 李言郡; 马海然

    2016-01-01

    目的:研究胶态微晶纤维素(microcrystalline cellulose, MCC)的流变特性及在中性乳饮料中的应用。方法通过使用流变仪、粘度仪分析研究胶态微晶纤维素的特性,包括触变性、粘度、悬浮能力和对抗热的稳定性。以中性乳饮料为体系,并结合产品离心沉淀率和体系浊度保留率状况,归纳微晶纤维素作为稳定剂使用时的关键影响因素。结果中性乳饮料体系选择微晶纤维素作为稳定剂,产品最终的离心沉淀率大大下降,浊度保留率有所提高。结论微晶纤维素复配卡拉胶、结冷胶对中性乳饮料的稳定性有明显的改善。%Objective To investigate the rheological properties of the gel microcrystalline cellulose (MCC) and its application in neutral dairy beverage.MethodsThe properties including thixotropy, viscosity, suspending ability and thermal stability of microcrystalline cellulose were analyzed using rheometer and viscosity meter. Based on neutral beverage system, the key factors affecting the properties of stabilizer MCC were summarized by combining centrifugal sedimentation rate and system turbidity retention rate.ResultsWith a proper selection of MCC as the stabilizer in neutral dairy beverage system, the centrifugal sedimentation rate of final product greatly reduced with an increased turbidity retention rate.ConclusionMCC combined with carrageenan and gellan gum can improve the stability of the neutral dairy beverage.

  3. Characteristics of microcrystalline cellulose and its application in neutral dairy beverage%微晶纤维素特性及其在中性乳饮料中的应用研究

    Institute of Scientific and Technical Information of China (English)

    薛玉清; 舒成亮; 余立意; 杨忻怡; 欧凯; 李言郡; 马海然

    2016-01-01

    ABSTRACT:Objective To investigate the rheological properties of the gel microcrystalline cellulose (MCC) and its application in neutral dairy beverage. Methods The properties including thixotropy, viscosity, suspending ability and thermal stability of microcrystalline cellulose were analyzed using rheometer and viscosity meter. Based on neutral beverage system, the key factors affecting the properties of stabilizer MCC were summarized by combining centrifugal sedimentation rate and system turbidity retention rate. Results With a proper selection of MCC as the stabilizer in neutral dairy beverage system, the centrifugal sedimentation rate of final product greatly reduced with an increased turbidity retention rate. Conclusion MCC combined with carrageenan and gellan gum can improve the stability of the neutral dairy beverage.%目的:研究胶态微晶纤维素(microcrystalline cellulose, MCC)的流变特性及在中性乳饮料中的应用。方法通过使用流变仪、粘度仪分析研究胶态微晶纤维素的特性,包括触变性、粘度、悬浮能力和对抗热的稳定性。以中性乳饮料为体系,并结合产品离心沉淀率和体系浊度保留率状况,归纳微晶纤维素作为稳定剂使用时的关键影响因素。结果中性乳饮料体系选择微晶纤维素作为稳定剂,产品最终的离心沉淀率大大下降,浊度保留率有所提高。结论微晶纤维素复配卡拉胶、结冷胶对中性乳饮料的稳定性有明显的改善。

  4. 大豆皮胶态微晶纤维素的流变学性质研究%Study on the rheological properties of microcrystalline cellulose from soybean hulls

    Institute of Scientific and Technical Information of China (English)

    李爱军; 张丽君; 胡丽娜; 欧仕益

    2012-01-01

    研究了浓度、剪切速率、剪切时间、静置时间、温度、金属离子等对大豆皮胶态微晶纤维素溶液粘度的影响。结果表明:大豆皮胶态MCC在水中可形成凝胶,低浓度的凝胶(小于2%)具有触变性;大豆皮胶态MCC溶液具有典型的剪切稀变性、良好的时变性和热稳定性;二价金属离子会使大豆皮胶态MCC溶液的粘度显著下降,当其浓度达到0.15mol/L或以上时,其假塑性会降低。%Effects of thickness, shearing rate,temperature, metal ion, shearing and stewing time on the rheological characteristics of microcrystalline cellulose from soybean hull were studied in this paper. Results showed that colloidal microcrystalline cellulose from soybean hulls formed gel in water and the low concentration solution( less than 2%)had the character of thixtropy. The solutions of colloidal soybean hulls microcrystalline cellulose had pseudoplastic behaviour and good thermal stability. Bivalent metal ions made the viscosity of the solutions decrease a lot and when the concentrations of bivalent metal ions rose to O.lSmol/L or more,the pseudoplastic behavior of the solution reduced.

  5. Cellulose nanowhiskers from coconut husk fibers: effect of preparation conditions on their thermal and morphological behavior

    Science.gov (United States)

    Cellulose nanowhiskers were prepared by sulfuric acid hydrolysis from coconut husk fibers which had previously been submitted to a delignification process. The effects of preparation conditions on the thermal and morphological behavior of the nanocrystals were investigated. Cellulose nanowhisker sus...

  6. Preparation of food grade carboxymethyl cellulose from corn husk agrowaste.

    Science.gov (United States)

    Mondal, Md Ibrahim H; Yeasmin, Mst Sarmina; Rahman, Md Saifur

    2015-08-01

    Alpha-cellulose extracted from corn husks was used as the raw material for the production of food-grade carboxymethyl cellulose (CMC). Preparation of CMC from husk cellulose was carried out by an etherification process, using sodium hydroxide and monochloroacetic acid (MCA), with ethanol as the supporting medium. Characterizations of CMC were carried out by analyzing the spectra of FTIR, XRD patterns and SEM photomicrographs. Degree of substitution (DS) was determined with respect to particle size using chemical methods. Solubility, molecular weight and DS of CMC increased with decreased cellulose particle sizes. Microbiological testing of the prepared CMC was done by the pour plate method. Concentrations of heavy metals such as arsenic, lead, cadmium and mercury in the purified CMC were measured by Atomic Absorption Spectroscopy technique and found to be within the WHO/FAO recommended value. A comparative study with CMC available in the international market was conducted. The purity of the prepared CMC was higher, at 99.99% well above the purity of 99.5% for standard CMC. High purity CMC showed a yield 2.4 g/g with DS 2.41, water holding capacity 5.11 g/g, oil holding capacity 1.59 g/g. The obtained product is well suited for pharmaceutical and food additives.

  7. Preparation and characterization of transparent PMMA-cellulose-based nanocomposites.

    Science.gov (United States)

    Kiziltas, Esra Erbas; Kiziltas, Alper; Bollin, Shannon C; Gardner, Douglas J

    2015-01-01

    Nanocomposites of polymethylmethacrylate (PMMA) and cellulose were made by a solution casting method using acetone as the solvent. The nanofiber networks were prepared using three different types of cellulose nanofibers: (i) nanofibrillated cellulose (NFC), (ii) cellulose nanocrystals (CNC) and (iii) bacterial cellulose from nata de coca (NDC). The loading of cellulose nanofibrils in the PMMA varied between 0.25 and 0.5 wt%. The mechanical properties of the composites were evaluated using a dynamic mechanical thermal analyzer (DMTA). The flexural modulus of the nanocomposites reinforced with NDC at the 0.5 wt% loading level increased 23% compared to that of pure PMMA. The NFC composite also exhibited a slightly increased flexural strength around 60 MPa while PMMA had a flexural strength of 57 MPa. The addition of NDC increased the storage modulus (11%) compared to neat PMMA at room temperature while the storage modulus of PPMA/CNC nanocomposite containing 0.25 and 0.5 wt% cellulose increased about 46% and 260% to that of the pure PMMA at the glass transition temperature, respectively. Thermogravimetric analysis (TGA) indicated that there was no significant change in thermal stability of the composites. The UV-vis transmittance of the CNF nanocomposites decreased by 9% and 27% with the addition of 0.25 wt% CNC and NDC, respectively. This work is intended to spur research and development activity for application of CNF reinforced PMMA nanocomposites in applications such as: packaging, flexible screens, optically transparent films and light-weight transparent materials for ballistic protection.

  8. Chemical modification of cellulose extracted from sugarcane bagasse: Preparation of hydroxyethyl cellulose

    Directory of Open Access Journals (Sweden)

    E.S. Abdel-Halim

    2014-07-01

    Full Text Available Cellulose was extracted from sugarcane bagasse by alkaline extraction with sodium hydroxide followed by delignification/bleaching using sodium chlorite/hexamethylenetetramine system. Factors affecting extraction process, including sodium hydroxide concentration, hexamethylenetetramine concentration and temperature were studied and optimum conditions for alkaline extraction were found to be boiling finely ground bagasse under reflux in 1 N sodium hydroxide solution and then carrying out the delignification/bleaching treatment at 95 °C using 5 g/l sodium chlorite together with 0.02 g/l hexamethylenetetramine. The extracted cellulose was used in the preparation of hydroxyethyl cellulose through reaction with ethylene oxide in alkaline medium. Factors affecting the hydroxyethylation reaction, like sodium hydroxide concentration during the alkali formation step, ethylene oxide concentration, reaction temperature and reaction duration were studied. Optimum conditions for hydroxyethylation reaction were using 20% NaOH solution and 200% ethylene oxide (based on weight of cellulose, carrying out the reaction at 100 °C for 60 min.

  9. Preparation of bacterial cellulose based hydrogels and their viscoelastic behavior

    OpenAIRE

    2015-01-01

    Bacterial cellulose (BC) based hydrogels have been prepared in blended with carboxymethylcellulose and polyvinyl pyrrolidone by using heat treatment. The properties of BC-CMC and BC-PVP hydrogels were compared with pure BC, CMC and PVP hydrogels. These hydrogels were investigated by measuring their structural, morphological and viscoelastic properties. Through the morphological images, alignment of the porous flake like structures could be seen clearly within the inter-polymeric network of th...

  10. Investigation on artificial blood vessels prepared from bacterial cellulose.

    Science.gov (United States)

    Zang, Shanshan; Zhang, Ran; Chen, Hua; Lu, Yudong; Zhou, Jianhai; Chang, Xiao; Qiu, Guixing; Wu, Zhihong; Yang, Guang

    2015-01-01

    BC (bacterial cellulose) exhibits quite distinctive properties than plant cellulose. The outstanding properties make BC a promising material for preparation of artificial blood vessel. By taking advantage of the high oxygen permeability of PDMS (polydimethylsiloxane) as a tubular template material, a series of BC tubes with a length of 100 mm, a thickness of 1mm and an outer diameter of 4 or 6mm were biosynthesized with the help of Gluconacetobacter xylinum. Through characterization by SEM (scanning electron microscope), tensile testing and thermal analysis, it is demonstrated that BC tubes are good enough for artificial blood vessel with elaborated nano-fiber architecture, qualified mechanical properties and high thermal stability. In addition, measurement of biocompatibility also shows that BC tubes are greatly adaptable to the in vivo environment. The results indicate that BC tubes have great potential for being utilized as tubular scaffold materials in the field of tissue engineering.

  11. Preparation of 14C Radiolabelled Sodium Carboxymethyl Cellulose

    Institute of Scientific and Technical Information of China (English)

    CHEN; Bao-jun; YANG; Hong-wei; LI; Shuai

    2013-01-01

    Carboxymethyl cellulose(CMC)is a kind of cellulose derivative.CMC has wide applications,including food,daily chemicals,pharmaceutical industry and chemical industry,etc.In order to study the metabolism of CMC,the sodium carboxymethyl cellulose was labelled with 14C.The carboxymethyl cellulose was labelled with 14C by treatment with alkalized cellulose and 14C-

  12. Investigation on artificial blood vessels prepared from bacterial cellulose

    Energy Technology Data Exchange (ETDEWEB)

    Zang, Shanshan; Zhang, Ran; Chen, Hua; Lu, Yudong; Zhou, Jianhai [Department of Biomedical Engineering, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074 (China); Chang, Xiao; Qiu, Guixing; Wu, Zhihong [Department of Orthopaedics, Peking Union Medical College Hospital, Beijing 100730 (China); Yang, Guang, E-mail: yang_sunny@yahoo.com [Department of Biomedical Engineering, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074 (China)

    2015-01-01

    BC (bacterial cellulose) exhibits quite distinctive properties than plant cellulose. The outstanding properties make BC a promising material for preparation of artificial blood vessel. By taking advantage of the high oxygen permeability of PDMS (polydimethylsiloxane) as a tubular template material, a series of BC tubes with a length of 100 mm, a thickness of 1 mm and an outer diameter of 4 or 6 mm were biosynthesized with the help of Gluconacetobacter xylinum. Through characterization by SEM (scanning electron microscope), tensile testing and thermal analysis, it is demonstrated that BC tubes are good enough for artificial blood vessel with elaborated nano-fiber architecture, qualified mechanical properties and high thermal stability. In addition, measurement of biocompatibility also shows that BC tubes are greatly adaptable to the in vivo environment. The results indicate that BC tubes have great potential for being utilized as tubular scaffold materials in the field of tissue engineering. - Highlights: • Bacterial cellulose (BC) can be made into tubular shape through PDMS mold. • BC represents a fine nanofiber network. • The mechanical and thermal properties of BC mimic the situation of real vessel. • BC exhibits attractive biocompatible properties as a substitution of vessel.

  13. A novel method for preparing microfibrillated cellulose from bamboo fibers

    Science.gov (United States)

    Dat Nguyen, Huu; Thanh Thuy Mai, Thi; Bich Nguyen, Ngoc; Duy Dang, Thanh; Loan Phung Le, My; Dang, Tan Tai; Tran, Van Man

    2013-03-01

    The bamboo fiber is a potential candidate for biomass and power source application. In this study, microfibrillated cellulose (MFC) is prepared from raw fibers of bamboo tree (Bambusa Blumeana J A & J H Schultes) by an alkali treatment at room temperature in association with a bleaching treatment followed by a sulfuric acid hydrolysis. Field-emission scanning electron microscopy (FESEM) images indicated that final products ranged from 20 to 40 nm in diameter. The chemical composition measurement and Fourier transform infrared (FTIR) spectroscopy showed that both hemicellulose and lignin are mostly removed in the MFC. The x-ray diffraction (XRD) results also show that MFC has crystallinity of more than 70%. The thermogravimetric analysis (TGA) curves revealed that cellulose microfibers have a two-step thermal decomposition behavior owing to the attachment of sulfated groups onto the cellulose surface in the hydrolysis process with sulfuric acid. The obtained MFCs may have potential applications in alternative power sources as biomass, in pharmaceutical and optical industries as additives, as well as in composite fields as a reinforcement phase.

  14. Immobilization of lysozyme-cellulose amide-linked conjugates on cellulose i and ii cotton nanocrystalline preparations

    Science.gov (United States)

    Lysozyme was attached through an amide linkage between some of the protein’s aspartate and glutamate residues to amino-glycine-cellulose (AGC), which was prepared by esterification of glycine to preparations of cotton nanocrystals (CNC). The nanocrystalline preparations were produced through acid h...

  15. Ionic Liquids and Cellulose: Dissolution, Chemical Modification and Preparation of New Cellulosic Materials

    Directory of Open Access Journals (Sweden)

    Mehmet Isik

    2014-07-01

    Full Text Available Due to its abundance and a wide range of beneficial physical and chemical properties, cellulose has become very popular in order to produce materials for various applications. This review summarizes the recent advances in the development of new cellulose materials and technologies using ionic liquids. Dissolution of cellulose in ionic liquids has been used to develop new processing technologies, cellulose functionalization methods and new cellulose materials including blends, composites, fibers and ion gels.

  16. Preparation and Characterisation of Amorphous-silicon Photovoltaic Devices Having Microcrystalline Emitters; Preparacion y Caracterizacion de Dispositivos Fotovoltaicos de Silicio Amorfo con Emisiones Microcristalinos

    Energy Technology Data Exchange (ETDEWEB)

    Gutierrez, M. T.; Gandia, J. J.; Carabe, J. [CIEMAT. Madrid (Spain)

    1999-11-01

    The present work summarises the essential aspects of the research carried out so far at CIEMAT on amorphous-silicon solar cells. The experience accumulated on the preparation and characterisation of amorphous and microcrystalline silicon has allowed to start from intrinsic (absorbent) and p-and n-type (emitters) materials not only having excellent optoelectronic properties, but enjoying certain technological advantages with respect to those developed by other groups. Among these are absorbent-layer growth rates between 5 and 10 times as fast as conventional ones and microcrystalline emitters prepared without using hydrogen. The preparation of amorphous-silicon cells has required the solution of a number of problems, such as those related to pinholes, edge leak currents and diffusion of metals into the semiconductor. Once such constraints have been overcome, it has been demonstrated not only that the amorphous-silicon technology developed at CIEMAT is valid for making solar cells, but also that the quality of the semiconductor material is good for the application according to the partial results obtained. The development of thin-film laser-scribing technology is considered essential. Additionally it has been concluded that cross contamination, originated by the fact of using a single-chamber reactor, is the basic factor limiting the quality of the cells developed at CIEMAT. The present research activity is highly focused on the solution of this problem. (Author)

  17. Preparation of cellulose II and III{sub I} films by allomorphic conversion of bacterial cellulose I pellicles

    Energy Technology Data Exchange (ETDEWEB)

    Faria-Tischer, Paula C.S., E-mail: paula.tischer@pq.cnpq.br [BioPol, Departamento de Química, UFPR, Cx. Postal 19081, 81531-980 Curitiba, PR (Brazil); Université Grenoble Alpes, Centre de Recherches sur les Macromolécules Végétales (CERMAV), F-38000 Grenoble (France); CNRS, CERMAV, F-38000 Grenoble (France); UMR 5628 (LMGP), CNRS and Grenoble Institute of Technology, 3 Parvis Louis Néel, F-38016 Grenoble Cedex 1 (France); Tischer, Cesar A. [BioPol, Departamento de Química, UFPR, Cx. Postal 19081, 81531-980 Curitiba, PR (Brazil); Université Grenoble Alpes, Centre de Recherches sur les Macromolécules Végétales (CERMAV), F-38000 Grenoble (France); CNRS, CERMAV, F-38000 Grenoble (France); CIME Nanotech, 3 Parvis Louis Néel, F-38016 Grenoble Cedex 1 (France); Heux, Laurent [Université Grenoble Alpes, Centre de Recherches sur les Macromolécules Végétales (CERMAV), F-38000 Grenoble (France); CNRS, CERMAV, F-38000 Grenoble (France); Le Denmat, Simon; Picart, Catherine [UMR 5628 (LMGP), CNRS and Grenoble Institute of Technology, 3 Parvis Louis Néel, F-38016 Grenoble Cedex 1 (France); Sierakowski, Maria-R. [BioPol, Departamento de Química, UFPR, Cx. Postal 19081, 81531-980 Curitiba, PR (Brazil); and others

    2015-06-01

    The structural changes resulting from the conversion of native cellulose I (Cel I) into allomorphs II (Cel II) and III{sub I} (Cel III{sub I}) have usually been studied using powder samples from plant or algal cellulose. In this work, the conversion of Cel I into Cel II and Cel III{sub I} was performed on bacterial cellulose films without any mechanical disruption. The surface texture of the films was observed by atomic force microscopy (AFM) and the morphology of the constituting cellulose ribbons, by transmission electron microscopy (TEM). The structural changes were characterized using solid-state NMR spectroscopy as well as X-ray and electron diffraction. The allomorphic change into Cel II and Cel III{sub I} resulted in films with different crystallinity, roughness and hydrophobic/hydrophilicity surface and the films remained intact during all process of allomorphic conversion. - Highlights: • Description of a method to modify the allomorphic structure of bacterial cellulose films • Preparation of films with specific morphologies and hydrophobic/hydrophilic surface characters • First report on cellulose III films from bacterial cellulose under swelling conditions • Detailed characterization of cellulose II and III films with complementary techniques • Development of films with specific properties as potential support for cells, enzymes, and drugs.

  18. Electro-mechanical properties of hydrogel composites with micro- and nano-cellulose fillers

    Science.gov (United States)

    N, Mohamed Shahid U.; Deshpande, Abhijit P.; Lakshmana Rao, C.

    2015-09-01

    Stimuli responsive cross-linked hydrogels are of great interest for applications in diverse fields such as sensors and biomaterials. In this study, we investigate polymer composites filled with cellulose fillers. The celluloses used in making the composites were a microcrystalline cellulose of commercial grade and cellulose nano-whiskers obtained through acid hydrolysis of microcrystalline cellulose. The filler concentration was varied and corresponding physical, mechanical and electro-mechanical characterization was carried out. The electro-mechanical properties were determined using a quasi-static method. The fillers not only enhance the mechanical properties of the composite by providing better reinforcement but also provide a quantitative electric potential in the composite. The measurements reveal that the polymer composites prepared from two different cellulose fillers possess a quantitative electric potential which can be utilized in biomedical applications. It is argued that the mechanism behind the quantitative electric potential in the composites is due to streaming potentials arising due to electrical double layer formation.

  19. Liquid crystalline solutions of cellulose in phosphoric acid for preparing cellulose yarns

    NARCIS (Netherlands)

    Boerstoel, H.

    2006-01-01

    The presen thesis describes a new process for manufacturing high tenacity and high modulus cellulose yarns. A new direct solvent for cellulose has been discovered, leading to liquid crystalline solutions. This new solvent, superphosphoric acid, rapidly dissolves cellulose. These liquid crystalline s

  20. Preparation of cellulose fibres with antibacterial Ag-loading nano-SiO2

    Indian Academy of Sciences (India)

    Wang Shuhua; Niu Runlin; Jia Husheng; Wei Liqiao; Daijinming; Liu Xuguang; Xu Bingshe

    2011-07-01

    The antibacterial cellulose fibres with acrylamide polymerization and Ag-loading SiO2 nanoantibacterial materials were successfully prepared. The chemical structures and morphologies of antibacterial cellulose fibres were characterized by Fourier transformation infrared spectrum (FTIR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The results showed that acrylamide was adsorbed on the surface of the cellulose fibres and formed a layer with thickness of 50–100 nm. The nano-SiO2 composite antibacterial materials were combined with cellulose fibres firmly by infiltrating into polyacrylamide layer about 100 nm. The antibacterial cellulose fibres with antibacterial layer owned excellent antibacterial effect.

  1. 微晶纤维素在食品工业中的应用研究进展%Research Development of the Application of Microcrystalline Cellulose in Food Industry

    Institute of Scientific and Technical Information of China (English)

    陆红佳; 郑龙辉; 刘雄

    2011-01-01

    微晶纤维素是由天然纤维素经水解至极限聚合度得到的白色粉末状物质,具有特殊的理化性质,被广泛的应用于化工、医药、食品等行业.文中主要综述了微晶纤维素的理化性质及其在食品工业中的应用,并对其发展前景进行了展望.%Microcrystalline cellulose(MCC) is produced by acid hydrolysis of natural cellulose to a level off degrees of polymerization(LODP).It had wide applications in food, pharmaceuticals, and other industries.This paper mainly reviews its physicochemical properties, its application in food industry, and the prospect of its future development.It also provides theoretical references for researchers for further in-depth study.

  2. Nanocrystalline cellulose from coir fiber: preparation, properties, and applications

    Science.gov (United States)

    Nanocrystalline cellulose derived from various botanical sources offers unique and potentially useful characteristics. In principle, any cellulosic material can be considered as a potential source of a nanocrystalline material, including crops, crop residues, and agroindustrial wastes. Because of t...

  3. Preparation and characterizations of cellulose-polylactic acid blending material%纤维素-聚乳酸共混改性膜材料的制备及其性能的研究

    Institute of Scientific and Technical Information of China (English)

    肖舒; 戴林; 申越; 何静

    2011-01-01

    将微晶纤维素溶于离子液体中,加入不同质量的聚乳酸,配制成共混溶液并成膜。通过红外光谱对其结构进行测定,证明共混物制备成功。X-衍射、SEM及DSC测试结果表明,共混物之间具有较好的相容性,当微晶纤维素与聚乳酸的质量比为60:40时共混效果较好,较易成膜,且二者的结晶过程得到互相促进,结晶完美度及晶体尺寸提高。同时,DSC测试结果表明,不同质量比的纤维素-聚乳酸共混物具有不同的结晶度,且纤维素与聚乳酸的质量比为60:40时亦具有较好的化学及生物降解性。%The cellulose-polylactie acid blending membrane was prepared via mixed solvent method.Firstly, microcrystalline cellulose was dissolved in ionic liquid,and then a different quality of polylactic acid was added. Infrared spectroscopy(FTIR) determined that blending membrane was prepared successfully.According to the results of X-ray diffraction,SEM and DSC,the microcrystalline cellulose and polylactic acid showed good compatibility with each other.When the mass ratio of microcrystalline cellulose to polylactic acid was 60:40,the membrane was easily obtained.At the same time,the crystallization process was promoted,and crystallization degree and crystal size were also increased.The results of DSC also showed that different mass ratio of cellulosepolylactic acid membrane had different degree of crystallinity.When the mass ratio of microcrystalline cellulose to polylactic acid was 60:40,the membrane also had good chemical and biological degradation.

  4. Preparation and Characterization of Cellulose Nanofibers from Two Commercial Hardwood and Softwood Pulps

    DEFF Research Database (Denmark)

    Stelte, Wolfgang; Sanadi, Anand R.

    2009-01-01

    The aim of this work was to study the mechanical fibrillation process for the preparation of cellulose nanofibers from two commercial hard- and softwood cellulose pulps. The process consisted of initial refining and subsequent high-pressure homogenization. The progress in fibrillation was studied...... using different microscopy techniques, mechanical testing, and fiber density measurements of cellulose films prepared after different processing stages. The mechanical properties of cellulose films showed an increase in strength and stiffness with decreasing fiber size, and this stabilized after...... a certain number of passes in the homogenizer. Atomic force microscopy studies showed that the obtained cellulose nanofibers had diameters in the 10−25-nm range. The significant difference between the two samples was that the ultimate failure strain for cellulose films made of softwood fibers increased...

  5. Preparation of carboxymethyl cellulose based microgels for cell encapsulation

    Directory of Open Access Journals (Sweden)

    Y. Ke

    2014-11-01

    Full Text Available Biocompatible and biodegradable carboxymethyl cellulose (CMC has been modified with 4-hydroxybenzylamine (CMC-Ph in order to prepare CMC-based microgels through the horseradish peroxidise/hydrogen peroxide enzymatic reaction. CMC-Ph was identified as a blend, and the amount of the grafted 4-hydroxybenzylamine per 100 units of CMC was between 17 and 23 according to the molecular weight of CMC. Through a special designed co-flowing microfluidic device, CMC-Ph microgels were prepared with the radius from 100 to 500 μm via adjusting the flow rates of the disperse phase and the continuous phase, respectively. The chondrocytic cell line ATDC5 was encapsulated in the CMC-Ph microgels. The cell-laden microgels were cultured for up to 40 days, illustrating the biocompatibility of CMC-Ph and the microfluidic approach through the enzymatic crosslinking reaction primarily. CMC-Ph showed a great promise to encapsulate the cells for further fabrication of the injectable scaffolds.

  6. Effects of Crystal Orientation on Cellulose Nanocrystals−Cellulose Acetate Nanocomposite Fibers Prepared by Dry Spinning

    Science.gov (United States)

    Si Chen; Greg Schueneman; R. Byron Pipes; Jeffrey Youngblood; Robert J. Moon

    2014-01-01

    This work presents the development of dry spun cellulose acetate (CA) fibers using cellulose nanocrystals (CNCs) as reinforcements. Increasing amounts of CNCs were dispersed into CA fibers in efforts to improve the tensile strength and elastic modulus of the fiber. A systematic characterization of dispersion of CNCs in the polymer fiber and their effect on the...

  7. Preparation and characterization of a novel micro- and nanocomposite hydrogels containing cellulosic fibrils

    Science.gov (United States)

    In recent years, the preparation of cellulosic composites and nanocomposites has become an important approach because of the wide abundance of cellulose, its biodegradability, renewability, and the ability to effectively reinforce a polymer matrix in an environmentally benign nature. The main object...

  8. Preparation of bacterial cellulose based hydrogels and their viscoelastic behavior

    Science.gov (United States)

    Shah, Rushita; Vyroubal, Radek; Fei, Haojei; Saha, Nabanita; Kitano, Takeshi; Saha, Petr

    2015-04-01

    Bacterial cellulose (BC) based hydrogels have been prepared in blended with carboxymethylcellulose and polyvinyl pyrrolidone by using heat treatment. The properties of BC-CMC and BC-PVP hydrogels were compared with pure BC, CMC and PVP hydrogels. These hydrogels were investigated by measuring their structural, morphological and viscoelastic properties. Through the morphological images, alignment of the porous flake like structures could be seen clearly within the inter-polymeric network of the hydrogels. Also, the detail structure analysis of the polymers blended during the hydrogel formation confirms their interactions with each other were studied. Further, the viscoelastic behavior of all the hydrogels in terms of elastic and viscous property was studied. It is observed that at 1% strain, including CMC and PVP hydrogels, all the BC based hydrogels exhibited the linear trend throughout. Also the elastic nature of the material remains high compared to viscous nature. Moreover, the changes could be noticed in case of blended polymer based hydrogels. The values of complex viscosity (η*) decreases with increase in angular frequency within the range of ω = 0.1-100 rad.s-1.

  9. Preparation and properties of cellulose nanocrystals reinforced collagen composite films.

    Science.gov (United States)

    Li, Weichang; Guo, Rui; Lan, Yong; Zhang, Yi; Xue, Wei; Zhang, Yuanming

    2014-04-01

    Collagen films have been widely used in the field of biomedical engineering. However, the poor mechanical properties of collagen have limited its application. Here, rod-like cellulose nanocrystals (CNCs) were fabricated and used to reinforce collagen films. A series of collagen/CNCs films were prepared by collagen solution with CNCs suspensions homogeneously dispersed at CNCs: collagen weight ratios of 1, 3, 5, 7, and 10. The morphology of the resulting films was analyzed by scanning electron microscopy (SEM), the enhancement of the thermomechanical properties of the collagen/CNCs composites were demonstrated by thermal gravimetric analysis (TGA) and mechanical testing. Among the CNCs contents used, a loading of 7 wt % led to the maximum mechanical properties for the collagen/CNCs composite films. In addition, in vitro cell culture studies revealed that the CNCs have no negative effect on the cell morphology, viability, and proliferation and possess good biocompatibility. We conclude that the incorporation of CNCs is a simple and promising way to reinforce collagen films without impairing biocompatibility. This study demonstrates that the composite films show good potential for use in the field of skin tissue engineering.

  10. Radiation preparation and swelling behavior of sodium carboxymethyl cellulose hydrogels

    Energy Technology Data Exchange (ETDEWEB)

    Liu Pengfei; Zhai Maolin; Li Jiuqiang; Peng Jing; Wu Jilan E-mail: wangwq@sun.ihep.ac.cn

    2002-03-01

    Sodium carboxymethyl cellulose (CMC) is a kind of degraded polymer under {gamma}-irradiation. However, in this work, it has been found that CMC crosslinks partially to form hydrogel by radiation technique at more than 20% CMC aqueous solution. The gel fraction increases with the dose. The crosslinking reaction of CMC is promoted in the presence of N{sub 2} or N{sub 2}O due to the increase of free radicals on CMC backbone, but gel fraction of CMC hydrogel is not high (<40%). Some important values related to this kind of new CMC hydrogel synthesized under different conditions, such as radiation yield of crosslinking G(x), gelation dose R{sub g}, number average molecular weight of network M{sub c} were calculated according to the Charlesby-Pinner equation. The results indicated that although crosslinked CMC hydrogel could be prepared by radiation method, the rate of radiation degradation of CMC was faster than that of radiation crosslinking due to the character of CMC itself. Swelling dynamics of CMC hydrogel and its swelling behavior at different conditions, such as acidic, basic, inorganic salt as well as temperature were also investigated. Strong acidity, strong basicity, small amount of inorganic salts and lower temperature can reduce swelling ratio.

  11. Preparation and characterization of aminosilane-functionalized cellulose nanocrystal aerogel

    Science.gov (United States)

    Wu, Yu; Cao, Fei; Jiang, Hua; Zhang, Yang

    2017-08-01

    In this study, cellulose nanocrystal (CNC) extracted from hybrid poplar residue was grafted with an aminosilane, N-(2-aminoethyl)-3-aminopropylmethyldimethoxysilane (AEAPMDS). Supercritical CO2 drying was employed to produce polymer aerogels. The effects of AEAPMDS on the properties of the aerogel were investigated. Fourier transform infrared spectroscopy confirmed that the aminosilane had been grafted on CNC. The crystallinity decreased due to the introduction of amorphous AEAPMDS on the surface of CNC. Analysis of specific surface areas and pore diameters indicated that the modification failed to destroy the inner structure of the aerogel. Scanning electron microscopy and thermogravimetry revealed that three-dimensional network structure was conserved after modification but had a lower thermal stability. High CO2 adsorption capacities (1.7 and 2.6 mmol g-1) were measured at 1 bar and two temperatures, 25 and 0 °C, respectively. Therefore, the modification procedure could be a promising avenue for the preparation of aminosilane-functionalized CNC aerogels as a novel adsorption material.

  12. Effect on Dissolvability of Microcrystalline Cellulose through Activation%微晶纤维素的活化对其溶解性能的影响

    Institute of Scientific and Technical Information of China (English)

    任丹; 李丹; 刘萍; 孙晓; 张瑞涵; 方健

    2012-01-01

    Microcrystalline cellulose(MCC) was activation treated by amine,water and ultrasonic respectively.The dissolve time in NaOH-Urea-Thiourea solution,degree of polymerization(DP),solubility,the surface of fiber,crystallinity and effect on molecule hydrogen bonding of MCC before and after activation were studied.The result showed that ultrasonic activation is better than the other two activation methods,which is more convenient to improve the dissolvability of MCC with treating power from 60 to 99 percent and treating time from 60 to 120 minutes.%用胺活化、水活化与超声波活化分别处理了微晶纤维素(MCC)。研究了活化前后微晶纤维素在氢氧化钠-尿素-硫脲中的溶解时间、聚合度、溶解度、纤维表面形态、结晶度以及对分子氢键的影响。结果表明,超声波活化较其他2种活化方法效果更好,且处理功率为60%~99%、处理时间在60~120min内更有利于改善微晶纤维素的溶解性能。

  13. Microcrystalline cellulose based matrix solid phase dispersion microextration for isomeric triterpenoid acids in loquat leaves by ultrahigh-performance liquid chromatography and quadrupole time-of-flight mass spectrometry.

    Science.gov (United States)

    Cao, Jun; Peng, Li-Qing; Xu, Jing-Jing

    2016-11-11

    An analytical procedure based on matrix solid phase dispersion (MSPD) microextration and ultrahigh-performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry was developed for the determination of isomeric triterpenoid acids (maslinic acid, corosolic acid, oleanolic acid and ursolic acid) in loquat leaves. Microcrystalline cellulose was used for the first time as a solid sorbent in MSPD microextration. Compared with the traditional extraction methods, the proposed method possessed the advantages of shorter extraction time, and lower consumption of sample, sorbent and organic solvent. The MSPD parameters that influenced the extraction efficiency of isomeric analytes were investigated and optimized in detail. Under the optimized conditions, good linearity was obtained with correlation coefficients higher than 0.9990. The limits of detection and quantification were 19.6-51.6μg/kg and 65.3-171.8μg/kg, respectively. Meanwhile, the recoveries obtained for all the analytes were ranging from 90.1% to 107.5%. Finally, the optimized method was successfully applied for analyzing these isomeric acids in loquat leaves samples obtained from different cultivated areas.

  14. A terahertz time-domain study on the estimation of opto-mechanical properties of pharmaceutical tablets using the Hashin-Shtrikman bounds for refractive index: a case study of microcrystalline cellulose and starch acetate compacts

    Science.gov (United States)

    Bawuah, Prince; Peiponen, Kai-Erik

    2016-06-01

    This work highlights the use of Hashin-Shtrikman (H-S) bounds in the prediction and verification of the effective refractive index, the height and the Young's modulus of given training sets of pharmaceutical compacts using the measured time delay of a THz pulse traversing the compacts. Set A consisted of 13 microcrystalline cellulose (MCC) compacts whereas set B was made up of 5 starch acetate (SA) compacts. MCC is a typical ingredient of many pharmaceutical tablets. In the case of the MCC compacts, tight and closely matched bounds were obtained between the experimental, the calculated upper, lower bound values for the effective refractive index, and the height values. This promising outcome has shown the high possibility of utilizing H-S bounds in the verification and prediction of the decision level of useful parameters, which can serve as a quality check for pharmaceutical tablets. For the SA compacts, although less tight bounds were observed, the experimental values for the effective refractive index and the Young's modulus were closely matched with the upper and the lower bounds, respectively. We therefore speculate based on the above observations that the MCC tablets contain an almost evenly distributed spherically shaped air voids whereas in the SA compacts, this assumption might not necessary be true.

  15. A METHOD OF PREPARING SPHERICAL NANO-CRYSTAL CELLULOSE WITH MIXED CRYSTALLINE FORMS OF CELLULOSE Ⅰ AND Ⅱ

    Institute of Scientific and Technical Information of China (English)

    Xiao-fang Li; En-yong Ding; Guo-kang Li

    2001-01-01

    A new kind of nano-crystal cellulose (NCC) prepared from natural cotton fiber has been obtained by the method of acid hydrolysis. Compared to most other nanophase materials that derive from inorganic materials, our products are prepared from natural cotton fibers. The products are of spherical shape with mixed crystal forms of cellulose Ⅰ and Ⅱ. The preparation conditions determine the properties of the products. Prior treatment is a critical procedure. The properties of the products are also strongly affected by such conditions as the kinds of acids used, the ratio of the acid mixture, the acid concentration, the ultrasonic agitation time and hydrolysis temperature. The number average molecular weight of NCC is determined by gel permeation chromatography (GPC). The particle size and shape were determined by transmission electron microscopy (TEM). X-ray diffraction was used to detect the crystallinity and average crystallite size of the particle.

  16. Poly(lactic acid)/natural rubber/cellulose nanocrystal bionanocomposites part I. Processing and morphology.

    Science.gov (United States)

    Bitinis, Natacha; Verdejo, Raquel; Bras, Julien; Fortunati, Elena; Kenny, Jose Maria; Torre, Luigi; López-Manchado, Miguel Angel

    2013-07-25

    PLA/NR/cellulose nanowhisker composites were prepared using three types of cellulose nanocrystals (CNC), i.e. unmodified CNC obtained from acid hydrolysis of microcrystalline cellulose and two surface modified CNC. The two modification reactions, consisting on the grafting of long alkyl chains and of PLA chains onto the cellulose nanocrystals were carried out in order to facilitate the incorporation of the nanocrystals in the PLA/NR blend. A novel processing method was optimized combining solvent casting and extrusion in order to obtain a homogeneous dispersion of the nanofillers in the blend. The CNC modifications determined their location in the PLA/NR blend and influenced its morphology.

  17. Physical properties and morphology of films prepared from microfibrillated cellulose and microfibrillated cellulose in combination with amylopectin

    DEFF Research Database (Denmark)

    Plackett, David; Anturi, Harvey; Hedenqvist, Mikael

    2010-01-01

    Two types of microfibrillated cellulose (MFC) were prepared using either a sulfite pulp containing a high amount of hemicellulose (MFC 1) or a carboxymethylated dissolving pulp (MFC 2). MFC gels were then combined with amylopectin solutions to produce solvent-cast MFC-reinforced amylopectin films...... to illustrate the morphology of MFC nanofibers in pure films and in an amylopectin matrix. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010...

  18. The preparation and study of cellulose carbamates and their regenerated membranes.

    Science.gov (United States)

    Yu, Guomin; Teng, Yun; Lai, Weidong; Yin, Cuiyu

    2016-12-01

    Using wood pulps with the average degree of polymerization 300-350 and urea as raw materials, cellulose carbamates were successfully synthesized by esterification reaction in N, N-dimethylacetamide(DMAc), an inexpensive, high boiling aprotic and polar solvent, for the purpose of improving the solubility of cellulose, reducing costs and environmental pollution. The products were dissolved in 9% sodium hydroxide solution at a low temperature after washing and drying and the cellulose carbamates solutions were obtained. The solutions were uniformly casted on a glass support after degassing. The regenerated cellulose membranes (CMs) were prepared by immersing the support in coagulation bath for some minutes. The structures of cellulose carbamates were characterized by Fourier transform infrared spectroscopy (FT-IR), (13)C solid state nuclear magnetic resonance spectrometry ((13)C NMR), Thermal gravimetric analysis(TG), Scanning electron microscopy (SEM) and X-ray diffractometry(XRD). The filtration performances of CMs were tested. The results reveal that part groups of cellulose were substituted by amino in the medium, the cellulose carbamates were prepared with the reducing crystallinity and thermal decomposition temperature. The CMs have good separation performance for methylene blue. Copyright © 2016 Elsevier B.V. All rights reserved.

  19. A novel ultrasonication method in the preparation of zirconium impregnated cellulose for effective fluoride adsorption.

    Science.gov (United States)

    Barathi, M; Kumar, A Santhana Krishna; Rajesh, N

    2014-05-01

    In the present work, we propose for the first time a novel ultrasound assisted methodology involving the impregnation of zirconium in a cellulose matrix. Fluoride from aqueous solution interacts with the cellulose hydroxyl groups and the cationic zirconium hydroxide. Ultrasonication ensures a green and quick alternative to the conventional time intensive method of preparation. The effectiveness of this process was confirmed by comprehensive characterization of zirconium impregnated cellulose (ZrIC) adsorbent using Fourier transform infrared spectroscopy (FT-IR), energy dispersive X-ray spectrometry (EDX) and X-ray diffraction (XRD) studies. The study of various adsorption isotherm models, kinetics and thermodynamics of the interaction validated the method.

  20. Preparation and characterization of bacterial cellulose nano crystals; Preparacao e caracterizacao de nanocristais de celulose bacteriana

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Daniele B. dos; Lima, Lais R. de; Barud, Hernane S.; Messaddeq, Younes; Ribeiro, Sidney J.L. [Universidade Estadual Paulista Julio de Mesquita Filho. Unesp, Instituto de Quimica, Araraquara, SP (Brazil)

    2011-07-01

    In this work we described the preparation of bacterial cellulose nano crystals (BCNC) by hydrolysis of bacterial cellulose with concentrated sulfuric acid. The influence of hydrolysis time in the nano crystals formation was evaluated and the materials characterized by scanning electron microscopy (SEM), thermogravimetric analysis (TG) and X-ray diffraction analysis. The SEM images showed the whiskers formation and its reveal that the morphology and size of BCNC not changes significantly with hydrolysis time. The X-rays diffractogram analysis showed an increase on BCNC crystallinity as compared with pure bacterial cellulose. The TG curves revealed a decreasing on thermal stability of BCNC samples with increase of the hydrolysis time. (author)

  1. Preparative displacement electrophoresis (isotachophoresis) of proteins on cellulose columns.

    Science.gov (United States)

    Johansson, G; Ofverstedt, L G; Hjertén, S

    1987-11-01

    This paper describes the separation of proteins by displacement electrophoresis on columns packed with cellulose powder as a stabilizing medium. Cellulose has virtually no molecular sieving properties and thus differs from dextran, polyacrylamide, and agarose in this respect. Therefore, without the risk of unstacking, columns packed with cellulose permit conventional elution of the protein zones and the use of a counter flow (to increase the effective length of the bed). For the same reason, electroosmotic flow is less disturbing. A continuous elution-migration technique adapted to suit the special requirements of displacement electrophoresis gave better separation than was obtainable by conventional elution. Normal human serum and a fresh hemolysate from human erythrocytes were used as samples. An expression for the volume velocity of the boundaries is derived. This parameter can be used to determine the maximum duration of a run and a suitable pump speed when continuous elution or a counter flow is employed. The special advantages of displacement electrophoresis in cellulose beds are discussed as well as general disadvantages of the displacement technique, including the risk that proteins precipitate during a run.

  2. Hot-wire chemical vapor deposition prepared aluminum doped p-type microcrystalline silicon carbide window layers for thin film silicon solar cells

    Science.gov (United States)

    Chen, Tao; Köhler, Florian; Heidt, Anna; Carius, Reinhard; Finger, Friedhelm

    2014-01-01

    Al-doped p-type microcrystalline silicon carbide (µc-SiC:H) thin films were deposited by hot-wire chemical vapor deposition at substrate temperatures below 400 °C. Monomethylsilane (MMS) highly diluted in hydrogen was used as the SiC source in favor of SiC deposition in a stoichiometric form. Aluminum (Al) introduced from trimethylaluminum (TMAl) was used as the p-type dopant. The material property of Al-doped p-type µc-SiC:H thin films deposited with different deposition pressure and filament temperature was investigated in this work. Such µc-SiC:H material is of mainly cubic (3C) SiC polytype. For certain conditions, like high deposition pressure and high filament temperature, additional hexagonal phase and/or stacking faults can be observed. P-type µc-SiC:H thin films with optical band gap E04 ranging from 2.0 to 2.8 eV and dark conductivity ranging from 10-5 to 0.1 S/cm can be prepared. Such transparent and conductive p-type µc-SiC:H thin films were applied in thin film silicon solar cells as the window layer, resulting in an improved quantum efficiency at wavelengths below 480 nm.

  3. Preparation and characterization of oil palm frond based cellulose hydrogel and its swelling properties

    Science.gov (United States)

    Selvakumaran, Nesha; Lazim, Mohd Azwani Shah bin Mat

    2016-11-01

    Malaysia is one of the largest producer of palm oil thus the quantity of biomass each year from this industry is very large. The oil palm frond from palm oil industry can be used as a source of cellulose which can be incorporated into hydrogel to be used as adsorbent. This research reported how to disperse 2 % cellulose in a `green-solution' prepared by using urea and sodium hydroxide. Polymerization is carried out between the monomers polyacrylamide and cellulose using microwave to form hydrogel. Hydrogel with 2 % cellulose have a swelling index of 1814 %. Meanwhile, zero hydrogel which is made with only polyacrylamide has swelling index of 15 %. Scanning electron microscope shows that cellulose hydrogel have a rough surface compared with zero hydrogel. This might attribute to the high swelling index for cellulose hydrogel compared with zero hydrogel. Meanwhile, FTIR shows that successful polymerization has occurred between polyacrylamide and cellulose with the characteristic band at 1657.99 cm-1 which is for N-H bond.

  4. Preparation and characterization of nano-cellulose with new shape from different precursor.

    Science.gov (United States)

    Maiti, Sonakshi; Jayaramudu, J; Das, Kunal; Reddy, Siva Mohan; Sadiku, Rotimi; Ray, Suprakas Sinha; Liu, Dagang

    2013-10-15

    Three different precursor materials - 1. China cotton, 2. South African cotton, 3. Waste tissue papers were used to produce nano-cellulose by acid hydrolysis route. No chemical pretreatment has been done for the production of nano-cellulose from these precursors. Prepared nano-cellulose and their corresponding precursor materials were characterized by transmission electron microscopy (TEM), particle size analysis, X-ray diffraction (XRD) study, thermo gravimetric analysis (TGA), differential scanning calorimetric (DSC) analysis and Fourier transformed infra red (FTIR) spectroscopy. A comparative study of the characteristics was done with the properties of raw materials and with that of nano-cellulose. Shape and size of the nano cellulose generally depends on nature of the precursor and hydrolysis condition. Morphology study of nano-cellulose from different sources revealed range of length from 50 to 200 nm and diameter from 10 to 90 nm. Higher thermal stability and crystallinity of nano-cellulose were observed compared to that of precursor from TGA/DSC study.

  5. Porous cellulose spheres: Preparation, modification and adsorption properties.

    Science.gov (United States)

    Ma, Xiaofei; Liu, Congzhi; Anderson, Debbie P; Chang, Peter R

    2016-12-01

    Porous cellulose spheres (PCS) were fabricated by precipitating the spheres from a cellulose ionic liquid solution, followed by freezing, solvent exchange, and drying. PCS had low crystallinity and a large surface area that facilitated modification with trisodium trimetaphosphate (STMP) to introduce phosphate ester groups into the porous structure of the heterogeneous system. The STMP-modified PCS (SPCS) were used to remove heavy metal ions from aqueous solution. With increasing STMP dosage, the adsorption capacity of SPCS obviously improved due to chelation between Pb(2+) and phosphate ester groups. The kinetic adsorption and isotherm data matched the pseudo-second order model and the Langmuir model well. The maximum adsorption capacity reached 150.6 mg g(-1) for SPCS. SPCS were competitive with other absorbents because the phosphate ester groups and porous structure contributed to Pb(2+) adsorption. Moreover, SPCS can be regenerated with ethylenediamine tetraacetic acid disodium salt (EDTA) solution for repetitious adsorption of Pb(2+).

  6. Improved Procedure for Preparation of Covalently Bonded Cellulose Tris-phenylcarbamate Chiral Stationary Phases

    Institute of Scientific and Technical Information of China (English)

    秦峰; 陈小明; 刘月启; 邹汉法; 王俊德

    2005-01-01

    The classical method for preparation of covalently boned cellulose derivative chiral stationary phases (CSP) with diisocyanate as spacer was improved. Diisocyanate was firstly allowed to react with 3-aminopropyltriethoxysilane, and the resulting product was then applied as the spacer reagent to immobilize cellulose derivatives onto silica gel. Influences of the amount and the length of the spacer on the optical resolution ability of the CSP were investigated. Comparing improved procedure to classical diisocyanate method, the cross-linking between the glucose units of the cellulose derivatives was avoided to the most extent. With the improved procedure, regio-nonselective ways could be adooted to prepare covalently bonded CSP, which showed an advantage for the rapid preparation.

  7. Cellulose acetate fibers prepared from different raw materials with rapid synthesis method.

    Science.gov (United States)

    Chen, Jinghuan; Xu, Jikun; Wang, Kun; Cao, Xuefei; Sun, Runcang

    2016-02-10

    Transesterification is a mild process to prepare cellulose acetate (CA) as compared with the traditional method. In this study, CA fibers were produced from six cellulose raw materials based on a simple and rapid transesterification method. The properties of the CA solutions and the obtained CA fibers were investigated in detail. Results showed that all of the cellulose raw materials were esterified within 15 min, and spinning dopes could be obtained by concentrating the CA solutions via vacuum distillation. The XRD, FT-IR, (1)H, (13)C and HSQC NMR analysis confirmed the successful synthesis of CA. The degree of substitution (DS) of the obtained CA was significantly affected by the degree of polymerization (DP) of cellulose raw materials, which further influenced the viscosity of CA solutions as well as the structural, thermal and mechanical properties of the CA fibers.

  8. Highly flexible magnetic composite aerogels prepared by using cellulose nanofibril networks as templates.

    Science.gov (United States)

    Liu, Shilin; Yan, Qiufang; Tao, Dandan; Yu, Tengfei; Liu, Xiaoya

    2012-06-20

    Nanostructured cellulose nanofibrils can form ductile or tough networks that are suitable templates for the creation of materials with functional properties. In this work, a facile method has been developed for the preparation of magnetic hybrid cellulose aerogels. The preparation processes followed by two steps, firstly, preparation of cellulose hydrogel films from LiOH/urea solvent, then CoFe2O4 nanoparticles were synthesized in the porous structured cellulose scaffolds. After being freeze-dried, CoFe2O4/cellulose magnetic aerogels were obtained. The porosity of the composite aerogels ranged from 78 to 52% with pore size distribution in a few tens of nanometers. The internal specific surface areas were around 300-320 m2/g, and the densities were in the range of 0.25-0.39 g/cm3. The hybrid aerogels showed improved mechanical strength, superparamagnetic properties. Unlike solvent-swollen gels and ferrogels, the magnetic composite aerogels were lightweight, flexibility, high porosity and with large specific surface area and could be expected to be used in many fields. Copyright © 2012 Elsevier Ltd. All rights reserved.

  9. A novel approach for the preparation of nanocrystalline cellulose by using phosphotungstic acid.

    Science.gov (United States)

    Liu, Yefei; Wang, Haisong; Yu, Guang; Yu, Qingxue; Li, Bin; Mu, Xindong

    2014-09-22

    In this work, a sustainable and green process to prepare nanocrystalline cellulose (NCC) from bleached hardwood pulp was demonstrated. Rod-like nanocrystalline cellulose with the size of 15-40 nm in width and hundreds of nanometers in length was obtained through H3PW12O40 (HPW)-catalyzed hydrolysis of bleached pulp fibers under the mild reaction conditions. Thermogravimetric analysis revealed that the resulting NCC exhibited much higher thermal stability than the partially sulfated NCC (prepared by sulfuric acid). In addition, the concentrated HPW could be easily recovered and recycled through the extraction with diethyl ether, and the recovered HPW could be reused for several rounds of cellulose hydrolysis without activity lost. These fundamental studies are of crucial importance for the development and application of NCC products/NCC-based biomaterials with good thermal stability.

  10. Preparation and Characterization of Cellulose and Nanocellulose from Agro-industrial Waste - Cassava Peel

    Science.gov (United States)

    Widiarto, S.; Yuwono, S. D.; Rochliadi, A.; Arcana, I. M.

    2017-02-01

    Cassava peel is an agro-industrial waste which is available in huge quantities in Lampung Province of Indonesia. This work was conducted to evaluate the potential of cassava peel as a source of cellulose and nanocellulose. Cellulose was extracted from cassava peel by using different chemical treatment, and the nanocellulose was prepared by hydrolysis with the use of sulfuric acid. The best methods of cellulose extraction from cassava peels are using alkali treatment followed by a bleaching process. The cellulose yield from this methods was 17.8% of dry base cassava peel, while the yield from nitric and sulfuric methods were about 10.78% and 10.32% of dry base cassava peel respectively. The hydrolysis was performed at the temperature of 50 °C for 2 hours. The intermediate reaction product obtained after each stage of the treatments was characterized. Fourier transform infrared spectroscopy showed the removal of non-cellulosic constituent. X-ray Diffraction (XRD) analysis revealed that the crystallinity of cellulose increased after hydrolysis. Morphological investigation was performed using Scanning Electron Microscopy (SEM). The size of particle was confirmed by Particle Size Analyzer (PSA) and Transmission Electron Microscopy (TEM).

  11. Preparation and characterization of regenerated cellulose membranes from natural cotton fiber

    Directory of Open Access Journals (Sweden)

    Yanjuan CAO

    2015-06-01

    Full Text Available A series of organic solutions with different cellulose concentrations are prepared by dissolving natural cotton fibers in lithium chloride/dimethyl acetamide (LiCl/DMAC solvent system after the activation of cotton fibers. Under different coagulating bath, the regenerated cellulose membranes are formed in two kinds of coagulation baths, and two coating methods including high-speed spin technique (KW-4A spin coating machine and low-speed scraping (AFA-Ⅱ Film Applicator are selected in this paper. The macromolecular structure, mechanical properties, crystallinity, thermal stability and wetting property of the regenerated cellulose membrane are characterized by Scanning Electron Microscope(SEM, Fourier Transform Infrared Spectroscopy (FT-IR,X-ray diffraction (XRD, Thermogravimetric analysis (TG and contacting angle tester. The effects of mass fraction, coagulation bath type, membrane forming process on the regenerated membrane properties are investigated. Experimental results show that the performance of regenerated cellulose membrane is relatively excellent under the condition of using the KW-4A high-speed spin method, water coagulation bath, and when mass fraction of cellulose is 3.5%. The crystallinity of the regenerated cellulose membrane changes a lot compared with natural cotton fibers. The variation trend of thermal stability is similar with that of cotton fiber. But thermal stability is reduced to some degree, while the wetting ability is improved obviously.

  12. A CHEMICAL PROCESS FOR PREPARING CELLULOSIC FIBERS HIERARCHICALLY FROM KENAF BAST FIBERS

    Directory of Open Access Journals (Sweden)

    Jinshu Shi

    2011-02-01

    Full Text Available The objective of this research was to evaluate an all-chemical process to prepare nano-scale to macro-scale cellulosic fibers from kenaf bast fibers, for polymer composite reinforcement. The procedure used in this all-chemical process included alkaline retting to obtain single cellulosic retted fiber, bleaching treatment to obtain delignified bleached fiber, and acidic hydrolysis to obtain both pure-cellulose microfiber and cellulose nanowhisker (CNW. At each step of this chemical process, the resultant fibers were characterized for crystallinity using X-ray diffraction (XRD, for functional groups using the Fourier Transform Infrared spectroscopy (FTIR, and for surface morphology using both the scanning electron microscopy (SEM and transmission electron microscopy (TEM. The chemical components of the different scale fibers were analyzed. Based on the raw kenaf bast fibers, the yields of retted fibers and bleached fibers were 44.6% and 41.4%. The yield of the pure cellulose microfibers was 26.3%. The yield of CNWs was 10.4%, where about 22.6% α-cellulose had been converted into CNWs. The fiber crystallinity increased as the scale of the fiber decreased, from 49.9% (retted single fibers to 83.9% (CNWs. The CNWs had fiber lengths of 100 nm to 1400 nm, diameters of 7 to 84 nm, and aspect ratios of 10 to 50. The incorporation of 9% (wt% CNWs in polyvinyl alcohol (PVA composites increased the tensile strength by 46%.

  13. Preparation of cellulose based microspheres by combining spray coagulating with spray drying.

    Science.gov (United States)

    Wang, Qiao; Fu, Aiping; Li, Hongliang; Liu, Jingquan; Guo, Peizhi; Zhao, Xiu Song; Xia, Lin Hua

    2014-10-13

    Porous microspheres of regenerated cellulose with size in range of 1-2 μm and composite microspheres of chitosan coated cellulose with size of 1-3 μm were obtained through a two-step spray-assisted approach. The spray coagulating process must combine with a spray drying step to guarantee the formation of stable microspheres of cellulose. This approach exhibits the following two main virtues. First, the preparation was performed using aqueous solution of cellulose as precursor in the absence of organic solvent and surfactant; Second, neither crosslinking agent nor separated crosslinking process was required for formation of stable microspheres. Moreover, the spray drying step also provided us with the chance to encapsulate guests into the resultant cellulose microspheres. The potential application of the cellulose microspheres acting as drug delivery vector has been studied in two PBS (phosphate-buffered saline) solution with pH values at 4.0 and 7.4 to mimic the environments of stomach and intestine, respectively.

  14. Microcrystalline Silicon Films and Solar Cells Prepared by Photochemical Vapor Deposition on Textured SnO2 with High Haze Factors

    Science.gov (United States)

    Zhao, Ying; Miyajima, Shinsuke; Ide, Yoshinori; Yamada, Akira; Konagai, Makoto

    2002-11-01

    Microcrystalline silicon (μc-Si) films and solar cells were prepared by mercury-sensitized photochemical vapor deposition (photo-CVD). The changes in the structural properties of a series of μc-Si films grown under various H2 dilution and deposition pressure conditions were discussed. The results indicated that the properties of μc-Si films depend strongly on the atomic hydrogen. The microstructures of μc-Si films on textured SnO2 with different haze factors (from 13% to 65%) were observed with a scanning electron microscope and a transmission electron microscope. The observations revealed that the μc-Si layers grew from the initial stage of deposition with columnar grains and that they were conformal to the surface of textured SnO2. The grain boundary density of μc-Si film on SnO2 with higher haze factors was lower than that on SnO2 with lower haze factors. The effect of textured SnO2 with different haze ratios on p-i-n μc-Si cell characteristics was discussed and it was found that the higher haze factors showed a higher degree of light trapping in our μc-Si cells. We deposited μc-Si cells with an intrinsic μc-Si layer thickness of 430 nm on a textured SnO2 sample with a haze factor of 42% and achieved a conversion efficiency of 6.55%.

  15. High coercivity microcrystalline Nd-rich Nd-Fe-Co-Al-B bulk magnets prepared by direct copper mold casting

    Science.gov (United States)

    Zhao, L. Z.; Hong, Y.; Fang, X. G.; Qiu, Z. G.; Zhong, X. C.; Gao, X. S.; Liu, Z. W.

    2016-06-01

    High coercivity Nd25Fe40Co20Al15-xBx (x=7-15) hard magnets were prepared by a simple process of injection casting. Different from many previous investigations on nanocomposite compositions, the magnets in this work contain hard magnetic Nd2(FeCoAl)14B, Nd-rich, and Nd1+ε(FeCo)4B4 phases. The magnetic properties, phase evolution, and microstructure of the as-cast and annealed magnets were investigated. As the boron content increased from 7 to 11 at%, the intrinsic coercivity Hcj of the as-cast magnet increased from 816 to 1140 kA/m. The magnets annealed at 750 °C have shown more regular and smaller grains than the as-cast alloys, especially for the x=11 alloy. The high intrinsic coercivities for the annealed alloys with x=8~11 result from the presence of small-sized grains in the microstructure. The highest Hcj of 1427 kA/m was obtained for the heat treated alloy with x=10. This work provides an alternative approach for preparing fully dense Nd-rich bulk hard magnets with relatively good properties.

  16. Preparation and characterization of cellulose acetate organic/inorganic hybrid films

    Science.gov (United States)

    Saeed S. Shojaie; Timothy G. Rials; Stephen S. Kelley

    1995-01-01

    A series of organic/inorganic hybrid (OIH) films were prepared using cellulose acetate (CA) as the organic component and tetraethyl orthosilicate (TEOS) as the inorganic component. The chemical, morphological, and mechanical properties of these films were evaluated with a variety of analytical techniques. The results of these evaluations showed that crosslinked CA OIH...

  17. Radiation preparation and swelling behavior of sodium carboxymethyl cellulose hydrogels

    Science.gov (United States)

    Liu, Pengfei; Zhai, Maolin; Li, Jiuqiang; Peng, Jing; Wu, Jilan

    2002-03-01

    Sodium carboxymethyl cellulose (CMC) is a kind of degraded polymer under γ-irradiation. However, in this work, it has been found that CMC crosslinks partially to form hydrogel by radiation technique at more than 20% CMC aqueous solution. The gel fraction increases with the dose. The crosslinking reaction of CMC is promoted in the presence of N 2 or N 2O due to the increase of free radicals on CMC backbone, but gel fraction of CMC hydrogel is not high (radiation crosslinking due to the character of CMC itself. Swelling dynamics of CMC hydrogel and its swelling behavior at different conditions, such as acidic, basic, inorganic salt as well as temperature were also investigated. Strong acidity, strong basicity, small amount of inorganic salts and lower temperature can reduce swelling ratio.

  18. Study on the Preparation and Characteristics of Cellulose/Silver Iodide Nanocomposite Film.

    Science.gov (United States)

    Lee, Yang Hun; Han, Sung Soo; Kang, Young Ah; Shin, Eun Joo

    2016-06-01

    In this study, the structure and properties of an organic-inorganic composite material prepared from cellulose doped with fine particles of silver iodide (AgI) were examined. The preparation of the composite involved the complexation of cellulose with polyiodide ions, such as I- and 13-, by immersion in iodine/potassium iodide (I2/KI: 0.2, 0.4, 0.6, 0.8, 1.0 M) or potassium iodide (KI: 0.6, 1.2, 1.8, 2.4, 3.0 M) aqueous solutions followed by reaction in a silver nitrate (AgNO3:1.0 M) aqueous solution. These procedures resulted in the in situ formation of fine β-AgI particles within the cellulose matrix. The characteristics and conductivities of prepared cellulose/silver iodide (AgI) nanocomposite films with different I2/KI and KI concentrations were investigated. AgI particle formation and aggregation increased on increasing I2/KI and KI concentrations as determined by SEM. X-ray results showed that KI could penetrate the cellulose crystal region and form AgI particles. The electrical conductivities of nanocomposite films treated with KI were higher than that of I2/KI at < 1.0 M of I2/KI and 3 M of KI, although the weight gain by AgI formation was lower than that of I2/KI. This was also attributed to the formation of smaller AgI particles and crystal defects. Highest electrical conductivity (3.8 x 10(-7) Ω(-1) cm(-1)) was obtained from the cellulose films (1.25 x 10(-11) Ω(-1) cm(-1)) treated with the aqueous solutions of 1.0 M I2/KI and 1.0 M AgNO3.

  19. Preparation of durable hydrophobic cellulose fabric from water glass and mixed organosilanes

    Science.gov (United States)

    Shang, Song-Min; Li, Zhengxiong; Xing, Yanjun; Xin, John H.; Tao, Xiao-Ming

    2010-12-01

    Durable superhydrophobic cellulose fabric was prepared from water glass and n-octadecyltriethoxysilane (ODTES) with 3-glycidyloxypropyltrimethoxysilane (GPTMS) as crosslinker by sol-gel method. The result showed that the addition of GPTMS could result in a better fixation of silica coating from water glass on cellulose fabric. The silanization of hydrolyzed ODTES at different temperatures and times was studied and optimized. The results showed that silanization time was more important than temperature in forming durable hydrophobic surface. The durability of superhydrophobicity treatment was analyzed by XPS. As a result, the superhydrophobic cotton treated under the optimal condition still remained hydrophobic properties after 50 washing cycles.

  20. Preparation and Determination of Drug-Polymer Interaction and In-vitro Release of Didanosine Microspheres made of Cellulose Acetate Phthalate or Ethyl cellulose Polymers

    OpenAIRE

    Sethi R. K; Barik B. B.; Sahoo S. K.

    2013-01-01

    The objective of this study was to formulate and evaluate the drug-polymer interaction of Didanosine using two polymers with different characteristics as Ethyl cellulose or Cellulose acetate phthalate. Microspheres were prepared by the emulsion solvent evaporation. The effect of drug-polymer interaction was studied for each of microspheres. Important parameters in the evaluation of a microencapsulation technique are encapsulation efficiency, yield production, particle size, surface characteri...

  1. Preparation and Application as the Filler for Elastomers of Flake-Shaped Cellulose Particles and Nanofibers

    Science.gov (United States)

    Nagatani, Asahiro; Lee, Seung-Hwan; Endo, Takashi; Tanaka, Tatsuya

    Fibrous cellulose made from wood pulp was mechanically milled into flake-shaped cellulose particles(FS-CPs) using a planetary ball mill with additives under several conditions. The average particle diameter of the FS-CPs was ca. 15μm, and the particles were available in a variety of thicknesses by changing the kind of the additives used in the milling process. FS-CPs-reinforced olefinic thermoplastic elastomer composites were prepared under melt mixing and passed through an open roll to orient the particles. The tensile modulus of the composites with a compatibilizer increased with increasing the particle content. The damping properties of the composites improved, compared to the neat elastomer. On the other hand, the fibrous cellulose was suspended in water, followed by wet disk-milled to prepare cellulose nanofibers(CNFs). The wet ground products showed nanoscopic fine morphology. CNFs-reinforced natural rubber(NR) composites were prepared by mixing the water suspension of CNFs with NR latex using a homogenizer. Then, it was dried in an oven and mixed again with vulcanizing ingredients of rubber using an open roll. The tensile properties of the composites improved remarkably by the addition of small amount of CNFs.

  2. MWCNTs/Cellulose Hydrogels Prepared from NaOH/Urea Aqueous Solution with Improved Mechanical Properties

    Directory of Open Access Journals (Sweden)

    Yingpu Zhang

    2015-01-01

    Full Text Available Novel high strength composite hydrogels were designed and synthesized by introducing multiwalled carbon nanotubes (MWCNTs into cellulose/NaOH/urea aqueous solution and then cross-linked by epichlorohydrin. MWCNTs were used to modify the matrix of cellulose. The structure and morphology of the hydrogels were characterized by Fourier transform infrared (FT-IR spectroscopy, high resolution transmission electron microscopy (HR-TEM, and scanning electron microscopy (SEM. The results from swelling testing revealed that the equilibrium swelling ratio of hydrogels decreased with the increment of MWCNTs content. Thermogravimetric analysis (TGA and dynamic mechanical analysis (DMA results demonstrated that the introduction of MWCNT into cellulose hydrogel networks remarkably improved both thermal and mechanical properties of the composite hydrogels. The preparation of MWCNTs modifiedcellulose-based composites with improved mechanical properties was the first important step towards the development of advanced functional materials.

  3. Preparation of membranes from cellulose obtained of sugarcane bagasse; Preparacao de membranas a partir de celulose obtida do bagaco de cana-de-acucar

    Energy Technology Data Exchange (ETDEWEB)

    Pereira, Paulo Henrique Fernandes; Cioffi, Maria Odila Hilario; Voorwald, Herman Jacobus Cornelis, E-mail: fernandes_eng@yahoo.com.b [UNESP, Guaratingueta, SP (Brazil). Fac. de Engenharia; Pinho, Maria Noberta de [Instituto Superior Tecnico de Lisboa (IST) (Portugal), Dept. de Engenharia; Silva, Maria Lucia Caetano Pinto da [Universidade de Sao Paulo (EEL/USP), Lorena, SP (Brazil). Escola de Engenharia

    2010-07-01

    In this work, cellulose obtained from sugarcane bagasse to produce both cellulose and acetylated cellulose to prepare asymmetric membranes. Membranes was procedure used a mixture of materials of DMAc/ LiCl systemic in different conditions. Cellulose and acetylated cellulose were characterized by thermogravimetric (TG), Xray diffraction (XRD) and scanning Electron Microscopy (SEM). Observed less stability thermal of acetylated cellulose when compared of cellulose. All membranes procedure were asymmetric, characterized by presence of a dense skin and porous support can be observed. SEM showed that the morphology of the superficial of membranes depends on the method preparation. (author)

  4. Cellulose aerogels prepared from an aqueous zinc chloride salt hydrate melt.

    Science.gov (United States)

    Schestakow, Maria; Karadagli, Ilknur; Ratke, Lorenz

    2016-02-10

    Monolithic cellulose aerogels are prepared using a salt hydrate melt based on cheap zinc chloride tetrahydrate (ZnCl2·4H2O) that can be washed out of the wet gel-body by using common solvents such as water, ethanol, isopropanol or acetone. Cellulose aerogels with concentrations of 1-5 wt.% cellulose were produced. These aerogels are characterized with respect to shrinkage, density and surface area as well as mechanical properties and micro-structure via SEM. Cellulose aerogels regenerated in acetone show a specific surface area of around 340 m(2)g(-1) being 60% higher than those regenerated in water. The onset of irreversible plastic deformation under compressive load is around 0.8 MPa for acetone-regenerated aerogels and thus a factor of two larger compared to ethanol regenerated ones. The Young's modulus depends almost linearly on the cellulose concentration which is observed for all regenerative fluids with the exception of water. The results achieved are presented in light of the polarity and ability of solvation of ZnCl2·4H2O in the regenerative fluids used.

  5. Regenerated cellulose/halloysite nanotube nanocomposite films prepared with an ionic liquid

    Energy Technology Data Exchange (ETDEWEB)

    Soheilmoghaddam, Mohammad [Department of Polymer Engineering, Faculty of Chemical Engineering, Universiti Teknologi Malaysia (UTM), Johor (Malaysia); Wahit, Mat Uzir, E-mail: mat.uzir@cheme.utm.my [Center for Composites, Universiti Teknologi Malaysia (UTM), 81310 Skudai, Johor (Malaysia); Mahmoudian, Shaya [Department of Textile Engineering, Kashan Branch, Islamic Azad University, Kashan (Iran, Islamic Republic of); Hanid, Nurbaiti Abdul [Department of Polymer Engineering, Faculty of Chemical Engineering, Universiti Teknologi Malaysia (UTM), Johor (Malaysia)

    2013-09-16

    Regenerated cellulose/halloysite nanotube (RC/HNT) nanocomposite films were successfully prepared in ionic liquid, 1-butyl-3-methylimidazolium chloride (BMIMCl) using solution casting method. The structural, morphological, thermal and mechanical properties of RC/HNT nanocomposites were investigated. X-ray diffraction analysis revealed a cellulose II crystalline structure and well dispersed HNT in RC/HNT nanocomposite films. At 6 wt.% HNT film, tensile strength and Young's modulus of RC films improved by 55.3% and 100%, respectively. Moisture absorption by the nanocomposites in an environment with 75% constant relative humidity was reduced by the addition of HNT to the RC. The presence of HNT enhanced the thermal stability and char yield of RC. The significant reinforcing effects of HNTs demonstrated that there is a possible interface interaction between cellulose and HNT which yielded better thermal and mechanical properties of the nanocomposite films as compared to pure RC. - Highlights: • The RC/HNT nanocomposite films were prepared via ionic liquid, BMIMCl. • XRD diffraction patterns and FESEM revealed well dispersed HNT in cellulose matrix. • The nanocomposite films exhibited excellent mechanical properties. • Moisture absorption and diffusion coefficient of RC reduced by HNT incorporation. • Addition of HNT enhanced thermal stability and activation energy of the RC.

  6. Green synthesis of a typical chiral stationary phase of cellulose-tris(3, 5-dimethylphenylcarbamate)

    Science.gov (United States)

    2013-01-01

    Background At present, the study on the homogeneous-phase derivatization of cellulose in ionic liquid is mainly focused on its acetylation. To the best of our knowledge, there has been no such report on the preparation of cellulose-tris(3,5-dimethylphenylcarbamate) (CDMPC) with ionic liquid 1-allyl-3-methyl-imidazolium chloride (AmimCl) so far. Results With ionic liquid 1-allyl-3-methylimidazolium chloride (AmimCl) as a reaction solvent, cellulose-tris(3,5-dimethylphenylcarbamate) (CDMPC) was synthesized by the reaction of 3,5-dimethylphenyl isocyanate and soluble microcrystalline cellulose in a homogeneous phase. The synthesized CDMPC was then coated onto the surfaces of aminopropyl silica gel to prepare a chiral stationary phase (CSP). The prepared CSP was successfully used in chiral separation of seven racemic pesticides by high performance liquid chromatography (HPLC). Good chiral separation was obtained using n-hexane and different modifiers as the mobile phases under the optimal percentage and column temperature, with the resolution of metalaxyl, diniconazole, flutriafol, paclobutrazol, hexaconazole, myclobutanil and hexythiazox of 1.73, 1.56, 1.26, 1.00, 1.18, 1.14 and 1.51, respectively. The experimental results suggested it was a good choice using a green solvent of AmimCl for cellulose functionalization. Conclusion CDMPC was successfully synthesized as the chiral selector by reacting 3, 5-dimethylphenyl isocyanate with dissolved microcrystalline cellulose in a green ionic liquid of AmimCl. PMID:23890199

  7. Method for depositing high-quality microcrystalline semiconductor materials

    Science.gov (United States)

    Guha, Subhendu; Yang, Chi C.; Yan, Baojie

    2011-03-08

    A process for the plasma deposition of a layer of a microcrystalline semiconductor material is carried out by energizing a process gas which includes a precursor of the semiconductor material and a diluent with electromagnetic energy so as to create a plasma therefrom. The plasma deposits a layer of the microcrystalline semiconductor material onto the substrate. The concentration of the diluent in the process gas is varied as a function of the thickness of the layer of microcrystalline semiconductor material which has been deposited. Also disclosed is the use of the process for the preparation of an N-I-P type photovoltaic device.

  8. The Preparation of Cellulose/Collagen Composite Films using 1-Ethyl-3-Methylimidazolium Acetate as a Solvent

    Directory of Open Access Journals (Sweden)

    Min Zhang

    2013-12-01

    Full Text Available Cellulose/collagen composite films with weight ratios of 30/1 (Blend-1 and 10/1 (Blend-2 were prepared using 1-ethyl-3-methylimidazolium acetate as a common solvent. The morphology of the films observed with a field-emission scanning electron microscope displayed a dependence on the ratio of cellulose/collagen. Collagen was successfully composited with cellulose without degradation and showed a denaturation temperature (Td higher than that of native collagen. Fourier transform infrared spectroscopy suggested that there were hydrogen-bond interactions between collagen and cellulose in the regenerated composite films. Thermogravimetric analysis revealed that the maximum decomposition temperature (Tmax of cellulose decreased after regeneration, while the Tmax of Blend-1 increased; however, it was reduced again for Blend-2. Elastic moduli from dynamic mechanical analysis exhibited a trend similar to that of Tmax. As indicated by X-ray diffraction, the distance between cellulose molecular chains was shortened for Blend-1 and elongated for Blend-2. Furthermore, the crystallization indices were calculated to be 75.3%, 68.3%, 66.2%, and 55.4% for native cellulose, regenerated films of cellulose, Blend-1, and Blend-2, respectively. These results confirm the dependence of the structural properties of composite films on cellulose/collagen ratios through the interactions between cellulose and collagen.

  9. Adsorption of Heavy Metals by Graphene Oxide/Cellulose Hydrogel Prepared from NaOH/Urea Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Xiong Chen

    2016-07-01

    Full Text Available By taking advantage of cellulose, graphene oxide (GO, and the process for crosslinking using epichlorohydrin (ECH, we propose a simple and novel method to prepare GO/cellulose hydrogel with good potential to adsorb metal ions. GO nanosheets containing carboxyl and hydroxyl groups were introduced into the surface of the cellulose hydrogel with retention of the gel structure and its nanoporous property. Due to the introduction of GO, the GO/cellulose composite hydrogels exhibited good compressive strength. Adsorption capacity of Cu2+ significantly increases with an increase in the GO/cellulose ratio and GO/cellulose hydrogel showed high adsorption rates. The calculated adsorption capacities at equilibrium ( q e cal for GO/cellulose hydrogel (GO:cellulose = 20:100 in weight was up to 94.34 mg·g−1, which was much higher than that of the pristine cellulose hydrogels. Furthermore, GO/cellulose hydrogel exhibited high efficient regeneration and metal ion recovery, and high adsorption capacity for Zn2+, Fe3+, and Pb2+.

  10. Effects of Ultrasound Irradiation on the Preparation of Ethyl Cellulose Nanocapsules Containing Spirooxazine Dye

    Directory of Open Access Journals (Sweden)

    Julija Volmajer Valh

    2017-01-01

    Full Text Available This article presents the influence of low frequency, high intensity ultrasonic irradiation on the characteristics (average size, polydispersity index of ethyl cellulose nanocapsules encapsulating a photochromic dye. Photochromic nanocapsules were prepared by the emulsion-solvent evaporation method. The acoustic densities entering the system were systematically studied with respect to their abilities to modify and reduce the average sizes and polydispersity indexes of the nanocapsules. Scanning electron microscope, confocal laser microscope, and dynamic light scattering were utilised to characterise the structure, shape, size, and polydispersity of ethyl cellulose photochromic nanocapsules. We were able to tailor the size of the photochromic nanocapsules simply by varying the acoustic densities entering the system. At an acoustic density of 1.5 W/mL and 60 s of continuous irradiation, we were able to prepare an almost monodispersed population of the nanocapsules with an average size of 193 nm.

  11. The Preparation of Salbutamol Sulfate Controlled Release TabletsCoated with Cellulose Acetate Aqueous Dispersion

    Institute of Scientific and Technical Information of China (English)

    ZhangFengyu; WuTao; PanWeisan; ChenJimin; ZhangRuhua

    2001-01-01

    In this study, emulsion-solvent evaporation method was applied to prepare the cellulose acetate(CA) aqueous dispersion. Upon the analyzing of the character of the aqueous dispersion, a controlled releaseformulation of salbutamol sulfate coated with cellulose acetate aqueous dispersion was prepared through orthogonalexperiment design. The factors that control the drug release character of the tablets were investigated. The drugrelease mechanism of the formulation was also studied. The experimental results indicated that CA aqueousdispersion had excellent film-forming ability under the effect of plasticizer. The drug release profile of the controlledrelease tablets coated with CA aqueous dispersion exhibited zero-order release character and the drug release rate wasmodulated by the osmotic pressure of the dissolution medium.

  12. Preparation of amino-functionalized regenerated cellulose membranes with high catalytic activity.

    Science.gov (United States)

    Wang, Wei; Bai, Qian; Liang, Tao; Bai, Huiyu; Liu, Xiaoya

    2017-09-01

    The modification of regenerated cellulose (RC) membranes was carried out by using silane coupling agents presenting primary and secondary amino-groups. The grafting of the amino groups onto the modified cellulose molecule was confirmed by X-ray photoelectron spectroscopies and (13)C nuclear magnetic resonance spectroscopic analyses. The crystallinity of the cellulose membranes (CM) decreased after chemical modification as indicated by the X-ray diffraction results. Moreover, a denser structure was observed at the surface and cross section of the modified membranes by SEM images. The contact angle measurements showed that the silane coupling treatment enhanced the hydrophobicity of the obtained materials. Then the catalytic properties of two types of modified membranes were studied in a batch process by evaluating their catalytic performance in a Knoevenagel condensation. The results indicated that the cellulose membrane grafted with many secondary amines exhibited a better catalytic activity compared to the one grafted only by primary amines. In addition, the compact structure of the modified membranes permitted their application in a pervaporation catalytic membrane reactor. Therefore, functional CM that prepared in this paper represented a promising material in the field of industrial catalysis. Copyright © 2017 Elsevier B.V. All rights reserved.

  13. Characterization and behavior of composite hydrogel prepared from bamboo shoot cellulose and β-cyclodextrin.

    Science.gov (United States)

    Liu, Shumin; Luo, Wenchao; Huang, Huihua

    2016-08-01

    Carboxymethyl cellulose was derived from bamboo shoot cellulose via chemical modification and was prepared into composite hydrogels by cross-linkage with β-cyclodextrin using epichlorohydrin as crossing agent. The structure of the prepared hydrogel was characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis and scanning electron microscopy. The results showed that the prepared composite hydrogel was sensitive to surrounding changes in pH value, temperature and ionic strength. Under the surroundings of low temperatures and high pH values, the prepared hydrogel had significant high swelling ratios (23338±988% at 15°C and 6937±112% at pH 8.0, respectively). In the solution of 0.1mol/L NaCl, the hydrogel showed the maximum water retention rate (48.73%). Sodium salicylate was used as the model drug to study the behaviors of hydrogel adsorption and release in simulated intestinal (at pH 7.4) and gastric liquid (at pH 1.8) surroundings. The prepared composite hydrogel exhibited higher drug release ratio in simulated intestinal liquid (63.09% after 380min) than in gastric liquid (22.09% after 400min). These pH responses of the prepared composite hydrogel showed its potential applications, especially as the drug carrier to attain control release of drugs under different surrounding conditions or organs in human body.

  14. Preparation and characterization of silver nanoparticles in methyl cellulose matrix and their antibacterial activity

    Science.gov (United States)

    Kolarova, Katerina; Samec, Daniel; Kvitek, Ondrej; Reznickova, Alena; Rimpelova, Silvie; Svorcik, Vaclav

    2017-06-01

    In this work we present in situ preparation of silver nanoparticles (NPs) by reduction of silver nitrate by methyl cellulose (MC). The aim of this study was to prepare a stable solution of MC-Ag, convert it to solid film, redissolve it and determine how this process influences the form and properties of the prepared NPs. MC was analysed by UV-vis spectrometry, transmission electron microscopy and X-ray photoelectron spectroscopy; it was studied in forms of a solution and as a solid film. We also evaluated the antibacterial activity and material properties of prepared films. Our results indicate that the size and distribution of particles are not negatively influenced by the conversion process. These findings can be used for preparation of antibacterial films or as a way of nanoparticle storage.

  15. Facile Method to Prepare Superhydrophobic and Water Repellent Cellulosic Paper

    Directory of Open Access Journals (Sweden)

    Ioannis Karapanagiotis

    2015-01-01

    Full Text Available Silica nanoparticles (7 nm were dispersed in solutions of a silane/siloxane mixture. The dispersions were applied, by brush, on four types of paper: (i modern, unprinted (blank paper, (ii modern paper where a text was printed using a common laser jet printer, (iii a handmade paper sheet detached from an old book, and (iv Japanese tissue paper. It is shown that superhydrophobicity and water repellency were achieved on the surface of the deposited films, when high particle concentrations were used (≥1% w/v, corresponding to high static (θS ≈ 162° and low tilt (θt < 3° contact angles. To interpret these results, scanning electron microscopy (SEM was employed to observe the surface morphologies of the siloxane-nanoparticle films. Static contact angles, measured on surfaces that were prepared from dilute dispersions (particle concentration <1% w/v, increased with particle concentration and attained a maximum value (162° which corresponds to superhydrophobicity. Increasing further the particle concentration did not have any effect on θS. Colourimetric measurements showed that the superhydrophobic films had negligible effects on the aesthetic appearance of the treated papers. Furthermore, it is shown that the superhydrophobic character of the siloxane-nanoparticle films was stable over a wide range of pH.

  16. Preparation and Characterization of Graphene Oxide / Cellulose Triacetate Forward Osmosis Membranes

    Directory of Open Access Journals (Sweden)

    Li Fang

    2016-01-01

    Full Text Available Forward osmosis (FO is an emerging membrane separation technology in environmental and industrial process. This paper presents cellulose triacetate (CTA membrane containing graphene oxide (GO nanosheets via blending to enhance membrane performance in forward osmosis (FO process. GO nanosheets with various loading were added into the casting solution to prepare the modified FO membranes. The prepared membranes were characterized by morphology analysis and permeability measurement. The result showed that the GO nanosheets effectively improved the performance of the CTA membranes. The CTA-0.2GO membrane had the highest water flux, reached 1.5 times as high as that of CTA membrane.

  17. Evaluation of roll compaction as a preparation method for hydroxypropyl cellulose-based matrix tablets

    Directory of Open Access Journals (Sweden)

    Imjak Jeon

    2011-01-01

    Full Text Available Roll compaction was applied for the preparation of hydroxypropyl cellulose (HPC-based sustained-release matrix tablets. Matrix tablets made via roll compaction exhibited higher dosage uniformity and faster drug release than direct-compacted tablets. HPC viscosity grade, roll pressure, and milling speed affected tablet properties significantly. Roll compaction seems to be an adequate granulation method for the preparation of HPC-based matrix tablets due to the simplicity of the process, less handling difficulty from HPC tackiness as well as easier particle size targeting. Selecting the optimum ratio of plastic excipients and the particle size of starting materials can however be critical issues in this method.

  18. Insights into the nucleation role of cellulose crystals during crystallization of poly(β-hydroxybutyrate).

    Science.gov (United States)

    Chen, Jianxiang; Xu, Chunjiang; Wu, Defeng; Pan, Keren; Qian, Aiwen; Sha, Yulu; Wang, Li; Tong, Wei

    2015-12-10

    Cellulose crystals, including microcrystalline cellulose (MCC) and nanocrystalline cellulose (NCC), were used as the fillers to prepare green composites with poly(β-hydroxybutyrate) (PHB) by melt mixing for crystallization study. The results reveal that the spherulite morphology of PHB and its composites depends highly on the crystallization temperature, evolving from bundle shaped to ring-banded and finally to irregular or zigzag textures with increase of temperature. However, the ring-banded structure is strongly affected by the presence of cellulose crystals, and the average band space decreases evidently with the addition of MCC or NCC. Compared with PHB/MCC composite, PHB/NCC composite shows degraded spherulite structure with smaller band space and higher flocculation level of peak-to-valley height because of stronger unbalanced stresses in this system. Besides, cellulose crystals can act as good heterogeneous nucleating agent to accelerate the crystallization of PHB, which is further confirmed by the polarized optical microscopy observations and the kinetic analyses.

  19. Cellulose aerogels prepared from cellulose/AmimCl solutions%以纤维素/AmimCl溶液制备纤维素气凝胶

    Institute of Scientific and Technical Information of China (English)

    吕玉霞; 李小艳; 米勤勇; 王德修; 余坚; 张军

    2011-01-01

    利用离子液体AmimC1溶解结合超临界CO2干燥的方法制备了纤维素气凝胶材料.研究了不同初始浓度的纤维素溶液及其在不同凝固浴中制备的纤维素凝胶的流变行为,进一步考察了纤维素溶液浓度和凝固浴种类对纤维素气凝胶材料结构的影响.结果表明,随着初始纤维素溶液浓度的增大,气凝胶的孔结构逐渐致密,比表面积随之减小;凝固浴的组成对纤维素气凝胶的结构也有较大影响.采用适当的制备条件,可以制备出高比表面积的纤维素气凝胶材料.对纤维素气凝胶的热性能进行了表征,结果表明所得到的气凝胶材料具有较好的热稳定性和较高的炭残余含量.%Cellulose aerogel materials were prepared by combining dissolving cellulose in an ionic liquid, 1-allyl-3-methylimidazolium chloride (AmimCl), and drying in supercritical CO2. The rheological properties of the cellulose solutions of different concentrations and their gels regenerated in different coagulation baths were studied. The porous structure and morphology of cellulose aerogels were found to be affected by cellulose concentration and nature of the coagulation bath. With increasing initial cellulose concentration, the porous structure of cellulose aerogels became more dense and uniform, leading to the gradual decrease of the specific surface area. Further, it was also observed that, both viscosity and the polarity of coagulation bath affected the structure of cellulose aerogels. High specific surface area cellulose aerogel materials could be prepared by controlling the experimental conditions. The obtained cellulose aerogels had relatively high char yield at elevated temperature, which makes them potential precursors for fabrication of novel mesoporous carbon materials.

  20. Preparation and physicochemical characterization of cellulose nanocrystals from industrial waste cotton

    Science.gov (United States)

    Thambiraj, S.; Ravi Shankaran, D.

    2017-08-01

    We aimed to develop a simple and low-cost method for the production of high-performance cellulose nanomaterials from renewable and sustainable resources. Here, cellulose microcrystals (CMCs) were prepared by controlled acidic and basic hydrolysis of cotton from textile industry wastes. The resulted CMCs were further converted into cellulose nanocrystals (CNCs) with high crystallinity by acidic hydrolysis. The physicochemical characteristics and morphological feature of CMCs and CNCs were studied by various analytical techniques such as UV-vis spectroscopy, Fourier-transform infrared spectroscopy (FT-IR), Scanning electron microscope (SEM), Fluorescence spectroscopy, Atomic force microscopy (AFM), High-resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The isolated CNCs possess a needle-like morphological structure with the longitudinal and lateral dimensions of 180 ± 60 nm, 10 ± 1 nm, respectively. The AFM result reveals that the CNCs have a high aspect ratio of 40 ± 14 nm and the average thickness of 6.5 nm. The XRD and TEM analysis indicate that the synthesized CNCs possess face-centered cubic crystal structure. Preliminary experiments were carried out to fabricate CNCs incorporated poly (vinyl alcohol) (PVA) film. The results suggest that the concept of waste to wealth could be well executed from the prepared CNCs, which have great potential for various applications including bio-sensors, food packaging and drug delivery applications.

  1. Porous starch/cellulose nanofibers composite prepared by salt leaching technique for tissue engineering.

    Science.gov (United States)

    Nasri-Nasrabadi, Bijan; Mehrasa, Mohammad; Rafienia, Mohammad; Bonakdar, Shahin; Behzad, Tayebeh; Gavanji, Shahin

    2014-08-08

    Starch/cellulose nanofibers composites with proper porosity pore size, mechanical strength, and biodegradability for cartilage tissue engineering have been reported in this study. The porous thermoplastic starch-based composites were prepared by combining film casting, salt leaching, and freeze drying methods. The diameter of 70% nanofibers was in the range of 40-90 nm. All samples had interconnected porous morphology; however an increase in pore interconnectivity was observed when the sodium chloride ratio was increased in the salt leaching. Scaffolds with the total porogen content of 70 wt% exhibited adequate mechanical properties for cartilage tissue engineering applications. The water uptake ratio of nanocomposites was remarkably enhanced by adding 10% cellulose nanofibers. The scaffolds were partially destroyed due to low in vitro degradation rate after more than 20 weeks. Cultivation of isolated rabbit chondrocytes on the fabricated scaffold proved that the incorporation of nanofibers in starch structure improves cell attachment and proliferation.

  2. Preparation and characterization of nanocrystalline cellulose from Acacia mangium and its reinforcement potential.

    Science.gov (United States)

    Jasmani, Latifah; Adnan, Sharmiza

    2017-04-01

    Acacia mangium, a fast growing tree is widely planted in Malaysia. Converting Acacia wood into nanocellulose could create new value added products for forest-based industry. Nanocrystalline cellulose (NCC) was prepared from Acacia mangium wood pulp via 64wt% sulfuric acid hydrolysis. Prior to acid hydrolysis, Acacia mangium was subjected to pulping followed by bleaching in order to remove non-cellulosic fragments. Acid hydrolysis was carried out on bleached pulp to produce the needle-like NCC with 79% crystallinity and aspect ratio of 26. The resulting NCC was mixed with PVA as a reinforcement material. Incorporation of 2% NCC improved the tensile of the NCC-PVA film by 30%. Copyright © 2016 Elsevier Ltd. All rights reserved.

  3. Preparation and characterization of cellulose paper/polypyrrole/bromophenol blue composites for disposable optical sensors

    Directory of Open Access Journals (Sweden)

    Gonçalves Débora

    2016-01-01

    Full Text Available This manuscript describes a novel approach for the preparation of composites based on cellulose paper (CP modified with polypyrrole (PPy and bromophenol blue (BPB (CP/PPy/BPB. Cellulose fibers are suitable for uniformly retaining the polymer in its doped form, once BPB can be used as a negatively charged dye. The CP/PPy/BPB composites were characterized by Raman Spectroscopy, Scanning Electron Microscopy, Spectroscopy and Dispersive Energy, and X-ray Diffraction. After characterization, they were studied for the quantification of pH and ammonia by diffuse reflectance spectroscopy. Under varying pH, different colors were verified, which ranged from yellow to blue, and an optical response for ammonia at concentrations as high as 25 ppm. The replacement of BPB by bromothymol blue (BTB did not produce efficient color transitions and showed no sensitivity to changes in pH and ammonia concentration.

  4. Cellulose-based graft copolymers prepared by simplified electrochemically mediated ATRP

    Directory of Open Access Journals (Sweden)

    P. Chmielarz

    2017-02-01

    Full Text Available Brush-shaped block copolymer with a dual hydrophilic poly(acrylic acid-block-poly(oligo(ethylene glycol acrylate (PAA-b-POEGA arms was synthesized for the first time via a simplified electrochemically mediated ATRP (seATRP under both constant potential electrolysis and constant current electrolysis conditions, utilizing only 30 ppm of catalyst complex. The polymerization conditions were optimized to provide fast reactions while employing low catalyst concentrations and preparation of cellulose-based brush-like copolymers with narrow molecular weight distributions. The results from proton nuclear magnetic resonance (1H NMR spectral studies support the formation of cellulose-based graft (copolymers. It is expected that these new polymer brushes may find application as pH- and thermo-sensitive drug delivery systems.

  5. Preparation, Characterization and Activity of a Peptide-Cellulosic Aerogel Protease Sensor from Cotton

    Directory of Open Access Journals (Sweden)

    J. Vincent Edwards

    2016-10-01

    Full Text Available Nanocellulosic aerogels (NA provide a lightweight biocompatible material with structural properties, like interconnected high porosity and specific surface area, suitable for biosensor design. We report here the preparation, characterization and activity of peptide-nanocellulose aerogels (PepNA made from unprocessed cotton and designed with protease detection activity. Low-density cellulosic aerogels were prepared from greige cotton by employing calcium thiocyanate octahydrate/lithium chloride as a direct cellulose dissolving medium. Subsequent casting, coagulation, solvent exchange and supercritical carbon dioxide drying afforded homogeneous cellulose II aerogels of fibrous morphology. The cotton-based aerogel had a porosity of 99% largely dominated by mesopores (2–50 nm and an internal surface of 163 m2·g−1. A fluorescent tripeptide-substrate (succinyl-alanine-proline-alanine-4-amino-7-methyl-coumarin was tethered to NA by (1 esterification of cellulose C6 surface hydroxyl groups with glycidyl-fluorenylmethyloxycarbonyl (FMOC, (2 deprotection and (3 coupling of the immobilized glycine with the tripeptide. Characterization of the NA and PepNA included techniques, such as elemental analysis, mass spectral analysis, attenuated total reflectance infrared imaging, nitrogen adsorption, scanning electron microscopy and bioactivity studies. The degree of substitution of the peptide analog attached to the anhydroglucose units of PepNA was 0.015. The findings from mass spectral analysis and attenuated total reflectance infrared imaging indicated that the peptide substrate was immobilized on to the surface of the NA. Nitrogen adsorption revealed a high specific surface area and a highly porous system, which supports the open porous structure observed from scanning electron microscopy images. Bioactivity studies of PepNA revealed a detection sensitivity of 0.13 units/milliliter for human neutrophil elastase, a diagnostic biomarker for inflammatory

  6. STUDY ON PREPARATION, COMPLEX PERMITTIVITY,PERMEABILITY AND MICROWAVE PROPERTIES OF BaZnzCo2- zFe16O27/SiO2 MICROCRYSTALLINE GLASS CERAMICS

    Institute of Scientific and Technical Information of China (English)

    H.J. Zhang; X.L. Jia; X. Yao; L. Y. Zhang

    2003-01-01

    BaZnz Co2- z Fe16 O27 /SiO2 microcrystalline glass ceramics with Z=0.0, 0.5, 0.8 and 1.1 were prepared at temperature 1200℃ for 5h by citrate sol-gel process. The complex dielectric constant and complex permeability of BaZnzCo2-zFe16O27/SiO2-paraffin wax composites had been measured. Both the complex dielectric constant and dielectric loss exhibit almost no variation with frequency in 0.1-6.0GHz. The real part of permeability decreases with increasing frequency for all samples, and the imaginary part of permeability exhibits a clear resonance peak at 1.44GHz for Co2 W/SiO2,1.32GHz for Zn0.5 Co1.5 W/SiO2, 1.20GHz for Zn0.8Co1.2 W/SiO2, and 1.08GHz for Zn1.1 Co0.9 W/SiO2. It is also showed that the content of zinc has a close effect on the magnetic properties of BaZnz Co2-zFe16 O27/SiO2 microcrystalline glass ceramics,the greater the zinc content, the higher the values of imaginary part of permeability and magnetic loss.

  7. Improved Cellulose Adsorption Method for the Preparation of Perovskite Oxides with Large Specific Surface Area at Low Temperature

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Perovskite-type La1-xSrxMO3-d (x=0,0.1,0.2, B=Co,Fe,Mn) oxides were prepared by pyrolysis of metal salt-(organic acid)-cellulose compound precursors. Low calcination temperatures, usually lower than 600oC, were needed. The specific surface area of the as-prepared oxides is higher than that prepared by the cellulose adsorption method, and is comparable to that prepared by sol-gel method. The effective organic acid could be EDTA acid, citric acid or DL-hydroxysuccinic acid, among them, EDTA acid is the best one.

  8. Stimuli-responsive cellulose modified by epoxy-functionalized polymer nanoparticles with photochromic and solvatochromic properties.

    Science.gov (United States)

    Abdollahi, Amin; Rad, Jaber Keyvan; Mahdavian, Ali Reza

    2016-10-05

    Photoresponsive papers are among the fast and simple tools for detection of polarity by solvatochromic and photochromic behaviors upon UV irradiation. Here, a new, green and facile modification strategy was employed to prepare novel stimuli-responsive cellulose materials containing spiropyran by mixing microcrystalline cellulose (MCC), as a model compound, with epoxy-functionalized photochromic latex. FTIR analysis, thermal and thermo-mechanical properties were used to confirm the microstructral properties. Crystallographic analysis revealed a decrease in crystallinity of cellulose matrix and approved the incorporation of photochromic copolymer. Then stimuli-responsive papers were prepared by using pulp paper as the cellulosic matrix and their smart characteristics were studied under UV irradiation while dried or immersed into some polar and non-polar solvents. Different color changes were observed and investigated by solid-state UV-vis spectroscopy. These significant results were attributed to the efficient chemical modification and confirmed by SEM, EDX and nitrogen mapping analyses.

  9. Preparation and properties of self-reinforced cellulose composite films from Agave microfibrils using an ionic liquid.

    Science.gov (United States)

    Reddy, K Obi; Zhang, Jinming; Zhang, Jun; Rajulu, A Varada

    2014-12-19

    The applications of natural fibers and their microfibrils are increasing rapidly due to their environment benefits, specific strength properties and renewability. In the present work, we successfully extracted cellulose microfibrils from Agave natural fibers by chemical method. The extracted microfibrils were characterized by chemical analysis. The cellulose microfibrils were found to dissolve in an ionic liquid 1-allyl-3-methylimidazolium chloride (AmimCl) to larger extent along with little quantity of undissolved microfibrils. Using this solution, the self-reinforced regenerated cellulose composite films were prepared. The raw fiber, extracted cellulose microfibrils and regenerated cellulose composite films were characterized by FTIR, (13)C CP-MAS NMR, XRD, TGA and SEM techniques. The average tensile strength, modulus and elongation at break of the self-reinforced cellulose composite films were found to be 135 MPa, 8150 MPa and 3.2%, respectively. The high values of tensile strength and modulus were attributed to the self-reinforcement of Agave fibers in their generated matrix. These self-reinforced cellulose biodegradable composite films prepared from renewable source can find applications in packaging field.

  10. Influence of coagulation bath on morphology of cellulose membranes prepared by NMMO method

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    To control the morphology of cellulose membranes used for separation,they were prepared by the NMMO method using water,methanol,ethanol and their binary solution as coagulation baths.Morphologies of the surface and cross section of dry membranes were observed.The pore structure parameters of wet membranes were determined.By comparison,the process and mechanism of pore formation in dry membranes were suggested,and the relativity of cellulose crystal size to average pore diameter in wet membranes and their influences were discussed.The results show that the morphology of dry membranes is clearly varied with coagulation baths,while the porosity of wet membranes is almost constant.Porous structures can appear in the compact region of dry membranes due to swelling from water.These pores have a virtual effect on the average pore diameter of wet membranes.By changing the composition of coagulation baths,the microstructure of cellulose membranes in a dry or wet environment can be adjusted separately.

  11. PREPARATION OF BIODEGRADABLE FLAX SHIVE CELLULOSE-BASED SUPERABSORBENT POLYMER UNDER MICROWAVE IRRADIATION

    Directory of Open Access Journals (Sweden)

    Hao Feng

    2010-05-01

    Full Text Available Superabsorbent polymer was prepared by graft polymerization of acrylic acid onto the chain of cellulose from flax shive by using potassium persulfate (KPS as an initiator and N,N’-methylenebisacrylamide (MBA as a crosslinker under microwave irradiation. SEM photographs were also studied for more information about the shive, cellulose from shive, and the superabsorbent polymer. The structure of the graft copolymer was confirmed by FT-IR spectroscopy and thermogravimetric analysis (TGA. The biodegradability in soil was measured at 32 and 40 oC. The polymer was porous, and thermal stability of the polymer was observed up to approximately 200 oC. FT-IR analysis indicated that acrylic acid in polymer was successfully grafted onto the cellulose. The graft copolymer was found to be an effective superabsorbent resin, rapidly absorbing water to almost 1000 times its own dry weight at pH around 7.3. The water absorbency in 0.9% NaCl, KCl, FeCl3 solutions and urine were 56.47 g/g, 54.71g/g, 9.89g/g and 797.21g/g, respectively. The product biologically degraded up to 40% at 40 oC in 54 days, which shows good biodegradability.

  12. Preparation of biocompatible magnetite-carboxymethyl cellulose nanocomposite: Characterization of nanocomposite by FTIR, XRD, FESEM and TEM

    Science.gov (United States)

    Habibi, Neda

    2014-10-01

    The preparation and characterization of magnetite-carboxymethyl cellulose nano-composite (M-CMC) material is described. Magnetite nano-particles were synthesized by a modified co-precipitation method using ferrous chloride tetrahydrate and ferric chloride hexahydrate in ammonium hydroxide solution. The M-CMC nano-composite particles were synthesized by embedding the magnetite nanoparticles inside carboxymethyl cellulose (CMC) using a freshly prepared mixture of Fe3O4 with CMC precursor. Morphology, particle size, and structural properties of magnetite-carboxymethyl cellulose nano-composite was accomplished using X-ray powder diffraction (XRD), transmission electron microscopy (TEM), Fourier transformed infrared (FTIR) and field emission scanning electron microscopy (FESEM) analysis. As a result, magnetite nano-particles with an average size of 35 nm were obtained. The biocompatible Fe3O4-carboxymethyl cellulose nano-composite particles obtained from the natural CMC polymers have a potential range of application in biomedical field.

  13. Porous Spherical Cellulose Composites Coated by Aluminum (Ⅲ) Oxide and Silicone: Preparation,Characterization and Adsorption Behavior

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Porous spherical cellulose composite (PSCA) coated by aluminum (Ⅲ) oxide was prepared andmodified by organosilicone. SEM images of the surface morphology of the bead cellulose shows that it hasspherical shape and abundant porous structure on its surface. The mapping images of aluminum and silicon ofthe composite (PSCAS) present aluminum( Ⅲ ) oxide and silicone are uniformly dispersed on the surface. Theadsorption behavior of PSCAS toward metal ions was determined.

  14. Preparation and microwave properties of Y-type magnetoplumbite microcrystalline glass ceramic with the composition 0.5(Ba{sub 2}Zn{sub Z}Co{sub 2-Z}Fe{sub 12}O{sub 22}).0.5SiO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, H.; Yao, X.; Zhang, L. [High Temperature Ceramics Inst., Zhengzhou Univ., Henan (China)

    2002-02-01

    The citrate sol-gel synthesis technique was used to prepared Ba{sub 2}Zn{sub Z}Co{sub 2-Z}Fe{sub 12}O{sub 22}/SiO{sub 2} microcrystalline glass ceramic with Z=2.0,1.6,1.2, and 0.8. Several methods such as X-ray diffractometry, scanning electron microscopy and HP vector network analyzer were used to obtain detailed information on the crystallography and magnetic properties of Ba{sub 2}Zn{sub Z}Co{sub 2-Z}Fe{sub 12}O{sub 22}/SiO{sub 2} microcrystalline glass ceramic. The correlation of the formation of Ba{sub 2}Zn{sub Z}Co{sub 2-Z}Fe{sub 12}O{sub 22}/SiO{sub 2} microcrystalline glass ceramic with thermal treatment was studied. The complex dielectric constant and complex permeability of microcrystalline glass ceramic-paraffin wax composites were measured by the transmission/reflection coaxial line method in the range from 100MHz to 6 GHz. The effects of composition, annealing temperature and measuring frequency on complex permittivity and permeability of Ba{sub 2}Zn{sub Z}Co{sub 2-Z}Fe{sub 12}O{sub 22}/SiO{sub 2} microcrystalline glass ceramic were also investigated. (orig.)

  15. SYNTHESIS AND CHARACTERIZATION OF CELLULOSE-SILICA COMPOSITE FIBER IN ETHANOL/WATER MIXED SOLVENTS

    Directory of Open Access Journals (Sweden)

    Ning Jia

    2011-04-01

    Full Text Available Cellulose-silica composite fiber samples have been successfully synthesized using cellulose solution, tetraethoxysilane, and NH3•H2O in ethanol/water mixed solvents at room temperature for 24 h. The cellulose solution was previously prepared by the dissolution of microcrystalline cellulose in a solvent mixture of N,N-dimethylacetamide (DMAc/lithium chloride (LiCl. The effect of the tetraethoxysilane concentration on the product was investigated. The products were characterized by X-ray powder diffraction (XRD, thermogravimetric analysis (TG, differential scanning calorimetric analysis (DSC, scanning electron microscopy (SEM, Fourier transform infrared spectrometry (FT-IR, energy-dispersive X-ray spectrum (EDS, and cross polarization magic angle spinning (CP/MAS solid state 13C-NMR. The morphology of the cellulose-silica composite fiber was investigated by SEM, while their composition was established from EDS measurements combined with the results of FT-IR spectral analysis and XRD patterns. The XRD, FT-IR and EDS results indicated that the obtained product was cellulose-silica composite fiber. The SEM micrographs showed that the silica particles were homogeneously dispersed in the cellulose fiber. The CP/MAS solid state 13C-NMR results indicated that the silica concentration had an influence on the crystallinity of the cellulose. This method is simple for preparation of cellulose-based composites.

  16. Preparation and characterization of nanocomposites of the carboxymethyl cellulose reinforced with cellulose nanocrystals; Preparacao e caracterizacao de nanocompositos de carboximetilcelulose reforcados com nanocristais de celulose

    Energy Technology Data Exchange (ETDEWEB)

    Flauzino Neto, Wilson P.; Silverio, Hudson A.; Vieira, Julia G.; Silva, Heden C.; Rosa, Joyce R.; Pasquini, Daniel, E-mail: wilsonpfneto@yahoo.com.br [Instituto de Quimica - Universidade Federal de Uberlandia - UFU, MG (Brazil); Assuncao, Rosana M.N. [Fac. de Ciencias Integradas do Pontal - FACIP, Universidade Federal de Uberlandia, Ituiutaba, MG (Brazil)

    2011-07-01

    Nanocrystals of cellulose (NCC) isolated from Eucalyptus urograndis Kraft pulp were used to prepare nanocomposites employing carboxymethyl cellulose (CMC) as matrix. The nanocrystals were isolated by hydrolysis with H{sub 2}SO{sub 4} 64% solution, for 20 minutes at 45 deg C. The nanocrystals were characterized by X-ray diffraction to evaluate the crystallinity of them. The amount of NCC used in the preparation of nanocomposites varied from 0 to 15%. The nanocomposites were characterized by thermal and mechanical analysis. A large reinforcing effect of NCC on the CMC matrix was observed. With the incorporation of the NCC, the tensile strength of nanocomposites was significantly improved by 107%, the elongation at break decreased by 48% and heat resistance to decomposition increased subtle. The improvement in thermo-mechanical properties are attributed to strong interactions between nanoparticles and CMC matrix. (author)

  17. Synthesis and characterization of a porous and hydrophobic cellulose-based composite for efficient and fast oil-water separation.

    Science.gov (United States)

    Wang, Xiangyun; Xu, Shimei; Tan, Yun; Du, Juan; Wang, Jide

    2016-04-20

    Oily wastewater is generated in diverse industrial processes, and its treatment has become crucial due to increasing environmental concerns. Herein, silanized cellulose was prepared by sol-gel reaction between microcrystalline cellulose (MCC) and hexadecyltrimethoxysilane (HDTMS) using for oil-water separation. The silanized cellulose was characterized by Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and thermal gravimetric analysis (TGA). A higher mass ratio of HDTMS to MCC made silanized cellulose become looser, and showed lower water absorbency. The silanized cellulose exhibited specific separation performance towards vegetable oil-water mixture (not for mineral oil-water mixture) with separation efficiency of 99.93%. Moreover, the separation was fast with a water flux of 4628.5Lm(-2)h(-1). The separation efficiency still remained at 99.77% even after recycling for 10 times.

  18. Preparation and characterization of poly(acrylic acid)-hydroxyethyl cellulose graft copolymer.

    Science.gov (United States)

    Abdel-Halim, E S

    2012-10-01

    Poly(acrylic acid) hydroxyethyl cellulose [poly(AA)-HEC] graft copolymer was prepared by polymerizing acrylic acid (AA) with hydroxyethyl cellulose (HEC) using potassium bromate/thiourea dioxide (KBrO(3)/TUD) as redox initiation system. The polymerization reaction was carried out under a variety of conditions including concentrations of AA, KBrO(3) and TUD, material to liquor ratio and polymerization temperature. The polymerization reaction was monitored by withdrawing samples from the reaction medium and measuring the total conversion. The rheological properties of the poly(AA)-HEC graft copolymer were investigated. The total conversion and rheological properties of the graft copolymer depended on the ratio of KBrO(3) to TUD and on acrylic acid concentration as well as temperature and material to liquor ratio. Optimum conditions of the graft copolymer preparation were 30 mmol KBrO(3) and 30 mmol TUD/100g HEC, 100% AA (based on weight of HEC), duration 2h at temperature 50 °C using a material to liquor ratio of 1:10.

  19. Preparation of hybrid nano biocomposite κ-carrageenan/cellulose nanocrystal/nanoclay

    Science.gov (United States)

    Zakuwan, Siti Zarina; Ahmad, Ishak; Ramli, Nazaruddin

    2013-11-01

    Biodegradable composites film based on κ-carrageenan and nano particles as filler was prepared to study the mechanical strength of carrageenan composites. Solution casting technique was used to prepare_this biocomposite. Preparation of composite film and nano filler involve two stages, preparation of cellulose nanocrystals (CNC) from kenaf with alkali treatment, bleaching, and hydrolysis followed by the preparation of two types of nano composite. Tensile test was carried on the composite film based on κ-carrageenan with the variation percentage of CNC and nano clay to obtain the optimum CNC and nano clay loading. After that hybrid nano-biocomposite film based on κ-carrageenan with the variation percentage of CNC/nano clay (OMMT) according to optimum value of composite carrageenan/CNC and composite carrageenan/nano clay film was prepared. The effect of nano filler on the mechanical properties of carrageenan films was examined. κ-carrageenan biocomposite increased with the optimum at 4% CNC and nano clay composition. Additional improvement of tensile strength with hybridization of CNC and nanoclay indicated better mechanical properties.

  20. Preparation and evaluation adsorption capacity of cellulose xanthate of sugarcane bagasse for removal heavy metal ion from aqueous solutions

    Science.gov (United States)

    Iryani, D. A.; Risthy, N. M.; Resagian, D. A.; Yuwono, S. D.; Hasanudin, U.

    2017-05-01

    The discharge of heavy metals from industrial effluents into aquatic system in surrounding area of Lampung bay become a serious problem today. The data shows that the concentrations of heavy metals in this area are above allowable limits for the discharge of toxic heavy metals in the aquatic systems. The most common of heavy metal pollutant is divalent metal ions. Cellulose xanthate is one of the selective adsorbent to solve this problem, since xanthate contains two negative sulfur atoms that is capable to catch divalent metal ions. Preparation of cellulose xanthate was conducted by reacting carbon disulfide (CS2) and cellulose from sugarcane bagasse. The morphological characteristics of cellulose xanthate were visualized via Scanning Electron Microscope (SEM) and the presence of sulfur groups on sugarcane bagasse xanthate were identified by FTIR spectroscopic study. The degree of substitution (DS), degree of polymerization (DP), and adsorption capacities of cellulose xanthate for Cu2+ and Pb2+ metal were studied. The results of study reveals that the maximum adsorption capacities of Cu2+ and Pb2+ metal on cellulose xanthate are 54.226 mg Cu2+/g, and 51.776 mg Pb2+/g, respectively. This study reveals that cellulose xanthate could be a solution to reduce environmental pollution caused by industrial wastewater.

  1. Preparation and Characterization of Palmitoyl Grafted Cellulose Nano Absorbent for the Efficient Adsorption of Pyrene from Aqueous Solution.

    Science.gov (United States)

    Jadhav, Arvind H; Mai, Xuan Thang; Appiah-Ntiamoah, Richard; Lee, Hanyeong; Momade, Francis W Y; Seo, Jeong Gil; Kim, Hern

    2015-10-01

    Palmitoyl grafted modified cellulose were prepared by simple chemical grafting method and applied as nano adsorbent for removal of pyrene from aqueous solution. The chemical properties and morphology of prepared nano-adsorbent were characterized by FT-IR, XRD, SEM, EDX, TGA, and contact angle. Results showed that palmitoyl successfully grafted on the surface of cellulose and possess effective organic functional groups for the adsorption of pyrene from aqueous solution. The adsorption performance of modified cellulose was significantly improved toward pyrene in aqueous solution. It is worthy to note that 0.25 g of palmitoyl grafted cellulose (PMC) removed 92% pyrene compared to unmodified cellulose which adsorbed 36% pyrene from 1.65 ppm aqueous solution of pyrene in very short contact time at room temperature. Results showed that, presence of various organic functional groups from palmitoyl chains grafted on cellulose backbone affected to pyrene removal. After completion of adsorption phenomenon nano-adsorbent can be removed by simply filtration process and reused several times. The adsorption capacity was studied under different experimental conditions and their effects on adsorption such as temperature, pH, and contact time were also studied. The kinetics and isotherms of material were also determined.

  2. High Performance Regenerated Cellulose Membranes from Trimethylsilyl Cellulose

    KAUST Repository

    Ali, Ola

    2013-05-01

    Regenerated cellulose (RC) membranes are extensively used in medical and pharmaceutical separation processes due to their biocompatibility, low fouling tendency and solvent resistant properties. They typically possess ultrafiltration and microfiltration separation characteristics, but recently, there have been attempts to widen their pool of applications in nanofiltration processes. In this work, a novel method for preparing high performance composite RC membranes was developed. These membranes reveal molecular weight cut-offs (MWCO) of less than 250 daltons, which possibly put them ahead of all commercial RC membranes and in competition with high performance nanofiltration membranes. The membranes were prepared by acidic hydrolysis of dip-coated trimethylsilyl cellulose (TMSC) films. TMSC, with a degree of silylation (DS) of 2.8, was prepared from microcrystalline cellulose by reaction with hexamethyldisilazane under the homogeneous conditions of LiCl/DMAC solvent system. Effects of parameters, such as coating solution concentration and drying rates, were investigated. It was concluded that higher TMSC concentrations as well as higher solvent evaporation rates favor better MWCOs, mainly due to increase in the selective layer thickness. Successful cross-linking of prepared membranes with glyoxal solutions, in the presence of boric acid as a catalyst, resulted in MWCOs less than 250 daltons. The suitability of this crosslinking reaction for large scale productions was already proven in the manufacturing of durable-press fabrics. For us, the inexpensive raw materials as well as the low reaction times and temperatures were of interest. Moreover, the non-toxic nature of glyoxal is a key advantage in medical and pharmaceutical applications. The membranes prepared in this work are strong candidates for separation of small organic solutes from organic solvents streams in pharmaceutical industries. Their hydrophilicity, compared to typical nanofiltration membranes, offer

  3. Biocomposites of cellulose reinforced starch: improvement of properties by photo-induced crosslinking.

    Science.gov (United States)

    Kumar, Annamalai Pratheep; Singh, Raj Pal

    2008-12-01

    In the present study, the composite films have been prepared from the aqueous dispersions of starch with microcrystalline cellulose using glycerol as plasticizer and irradiated under ultraviolet (UV) light using sodium benzoate as photo-sensitizer. Photo-crosslinking was characterized by measuring the water absorption under 100% relative humidity, swelling degree and gel fraction in dimethylsulphoxide (DMSO), upon irradiation time. Both, the incorporation of cellulose and photo-irradiation were found to decrease the water absorption, swelling in DMSO and increase the gel fraction. Thermal transitions indicated the anti-plasticization of amylopectin chains at the fiber/matrix interface. With increasing content of cellulose and photo-irradiation time, the tensile modulus and strength were found to improve. It is summarized that the combination of cellulose reinforcement and photo-crosslinking of matrix has improved the physical and mechanical properties.

  4. Preparing cationic cotton linter cellulose with high substitution degree by ultrasonic treatment.

    Science.gov (United States)

    Zhang, Fulong; Pang, Zhiqiang; Dong, Cuihua; Liu, Zong

    2015-11-05

    As an important cellulose derivative, cationic cellulose has becoming an attractive material. However, it remains challenging to produce cationic cellulose with high substitute degree. In this paper, we successfully increased the substitute degree of cationic cellulose by introducing ultrasonic treatment, which efficiently breaks hydrogen bonds of the chemical structure of cationic cellulose. Properties of cationic cellulose were studied by scanning electron spectroscope (SEM), contact angle, X-ray diffraction (XRD) and thermogravimetric analysis (TGA). Experimental results show that the cationic cellulose has rougher surface and lower crystallinity degree as compared to the original sample. TGA analysis verifies that the thermostability of CLC decreases after the cationic modification. The residual of the cationic cellulose (25 wt%) after pyrolysis increases significantly as compared to that of the original cellulose (15 wt%).

  5. FORMULATION OF FUROSEMIDE SOLID DISPERSION WITH MICRO CRYSTALLINE CELLULOSE FOR ACHIEVE RAPID DISSOLUTION

    Directory of Open Access Journals (Sweden)

    Rajanikant C. Patel

    2010-06-01

    Full Text Available Furosemide, a weekly acidic, loop diuretic drug indicated for treatment of edema and hypertension having high permeability through stomach. It is practically insoluble in gastric fluid (0.006 mg/mL and having highly permeability through stomach but due to its solubility limitation it can’t enter into systemic circulation. It was logically decided to design experiment, so as to achieve the set objectives. Attempt was made to prepare solid dispersion of furosemide with Poly ethylene glycol (PEG 6000 containing microcrystalline cellulose (MCC as adsorbent which would dissolve completely in less than 30 minutes (target selected by considering minimum gastric empting time. Microcrystalline cellulose converted sticky dispersion in to free flow powder hence increase surface area which responsible for dissolution improvement. Factorial design was applied to optimize formulation. Amount of poly ethylene glycol 6000 and microcrystalline cellulose were selected as an Independent variable while angle of repose and T100% were selected as dependent variable. Attempts for dissolution rate of furosemide improve bioavailability and consequently dose reduction would possible.

  6. SANS studies of solutions and molecular composites prepared from cellulose tricarbanilate

    CERN Document Server

    Alava, C; Cameron, J D; Cowie, J M G; Vaqueiro, P; Möller, A; Triolo, A

    2002-01-01

    We report on SANS measurements carried out on the instrument SANS1 (V4) at the BENSC facility on solutions and composites of cellulose tricarbanilate (CTC). This cellulose derivative exhibits lyotropic behaviour in methylacrylate (MA). The SANS data indicate that in the isotropic liquid state (up to 25% wt CTC in MA) the CTC chains behave like rods of mass per unit length (M/L). In the liquid crystalline (LC) phase (at and above 35% wt CTC in MA), the Q dependence varies from Q sup - sup 1 to Q sup - sup 4 , probably as a result of self-assembling of the CTC chains. The general aim of our work is to prepare molecular composites, i.e. miscible blends of rigid-rod and flexible-coil polymers, from CTC solutions in polymerizable media. To establish the degree of homogeneity of the composites, we performed SANS measurements on UV-cured CTC/MA solutions. Here, we compare the SANS data of CTC/monomer solutions with those of the corresponding composites. (orig.)

  7. Preparation of cellulose nanocrystals from Humulus japonicus stem and the influence of high temperature pretreatment.

    Science.gov (United States)

    Jiang, Yani; Zhou, Jiping; Zhang, Qi; Zhao, Guoqi; Heng, Lin; Chen, Dongdong; Liu, Dongfang

    2017-05-15

    As one of the most abundant wild herbs in nature, the Humulus japonicus stem (HJS) is a new low-cost source of cellulosic material. In this work, cellulose nanocrystals (CNCs) were isolated from HJS using acid hydrolysis. The influence of high temperature pretreatment (HT pretreatment) on the properties and yields of these HT-HJS (HJS fibers after HT pretreatment at different temperatures) and HT-CNCs (CNCs prepared from the HT-HJS) was studied. The results showed that there was no variation of the chemical structure among the HT-HJS and HT-CNCs. The thermal stabilities and crystallinities of the HT-HJS were higher than bleached HJS. The average diameters of the HT-CNCs were significantly smaller while the average aspect ratios of them were obviously bigger than the CNCs, and the biggest average aspect ratio of HT140-CNCs (63.40) was almost twice of CNCs (32.00). Compared with the CNCs (70.05%, 212.8°C), the crystallinity and initial degradation temperature also showed increase for the HT-CNCs and increased up to maximum of 86.93% and 227.5°C for the HT160-CNCs. Copyright © 2017 Elsevier Ltd. All rights reserved.

  8. SANS studies of solutions and molecular composites prepared from cellulose tricarbanilate

    Energy Technology Data Exchange (ETDEWEB)

    Alava, C.; Arrighi, V.; Cameron, J.D.; Cowie, J.M.G.; Vaqueiro, P. [Department of Chemistry, Heriot-Watt University, Edinburgh EH14 4AS (United Kingdom); Moeller, A.; Triolo, A. [Hahn-Meitner-Institut-BENSC, Glienicker Strasse 100, 14109 Berlin (Germany)

    2002-07-01

    We report on SANS measurements carried out on the instrument SANS1 (V4) at the BENSC facility on solutions and composites of cellulose tricarbanilate (CTC). This cellulose derivative exhibits lyotropic behaviour in methylacrylate (MA). The SANS data indicate that in the isotropic liquid state (up to 25% wt CTC in MA) the CTC chains behave like rods of mass per unit length (M/L). In the liquid crystalline (LC) phase (at and above 35% wt CTC in MA), the Q dependence varies from Q{sup -1} to Q{sup -4}, probably as a result of self-assembling of the CTC chains. The general aim of our work is to prepare molecular composites, i.e. miscible blends of rigid-rod and flexible-coil polymers, from CTC solutions in polymerizable media. To establish the degree of homogeneity of the composites, we performed SANS measurements on UV-cured CTC/MA solutions. Here, we compare the SANS data of CTC/monomer solutions with those of the corresponding composites. (orig.)

  9. Mechanical, Microstructure and Surface Characterizations of Carbon Fibers Prepared from Cellulose after Liquefying and Curing

    Directory of Open Access Journals (Sweden)

    Xiaojun Ma

    2013-12-01

    Full Text Available In this study, Cellulose-based carbon fibers (CBCFs were prepared from cellulose after phenol liquefaction and curing. The characteristics and properties of CBCFs were examined by scanning electron microscopy (SEM, Fourier transform infrared spectroscopy (FTIR, X-ray diffraction (XRD, Raman spectroscopy and X-ray photoelectron spectroscopy (XPS. The results showed that, with increasing carbonization temperature, the La, Lc, and Lc/d(002 of CBCFs increased gradually, whereas the degree of disorder R decreased. The –OH, –CH2–, –O–C– and phenyl group characteristic absorption peaks of CBCFs reduced gradually. The cross-linked structure of CBCFs was converted into a graphite structure with a six-ring carbon network during carbonization. The surface of CBCFs were mainly comprised of C–C, C–O, and C=O. The tensile strength, carbonization yield and carbon content of CBCFs obtained at 1000 °C were 1015 MPa, 52%, and 95.04%, respectively.

  10. Alexa Fluor-labeled Fluorescent Cellulose Nanocrystals for Bioimaging Solid Cellulose in Spatially Structured Microenvironments

    Energy Technology Data Exchange (ETDEWEB)

    Grate, Jay W.; Mo, Kai-For; Shin, Yongsoon; Vasdekis, Andreas; Warner, Marvin G.; Kelly, Ryan T.; Orr, Galya; Hu, Dehong; Dehoff, Karl J.; Brockman, Fred J.; Wilkins, Michael J.

    2015-03-18

    Cellulose nanocrystal materials have been labeled with modern Alexa Fluor dyes in a process that first links the dye to a cyanuric chloride molecule. Subsequent reaction with cellulose nanocrystals provides dyed solid microcrystalline cellulose material that can be used for bioimaging and suitable for deposition in films and spatially structured microenvironments. It is demonstrated with single molecular fluorescence microscopy that these films are subject to hydrolysis by cellulose enzymes.

  11. 十字型微通道制备粒径均一的纤维素层析介质%Preparation of cellulose-based chromatography matrix with uniform size by cross-flow microchannel chip

    Institute of Scientific and Technical Information of China (English)

    童芳丽; 林东强; 刘川; 贠军贤; 姚善泾

    2013-01-01

    为了满足层析介质对粒径单分散的要求,利用十字型微通道的聚焦效应,形成粒径均一的纤维素微液滴,经固化成纤维素微球,再偶联配基制成了纤维素层析介质.以离子液体1-乙基-3-甲基咪唑甲基磷酸直接溶解微晶纤维素为水相,葵花籽油为油相,考察了微通道内微液滴的形成条件,优化了纤维素浓度、分散剂浓度、油水两相流速等因素,得到粒径约100 μm的纤维素微液滴,CV值小于0.2.微液滴固化再生,得到球形度良好的纤维素微球,湿真密度1.019 g.ml-1,孔度94.6%,体均粒径105.5 μm;进一步偶联DEAE配基,制得了离子交换层析介质,离子交换容量为123.3 μmol·g-1,牛血清白蛋白的饱和吸附容量Qm达到220 mg·g-1,有效扩散系数De为1.8×10-11m2·s-1,体现出较好的蛋白质吸附性能.%To prepare the cellulose-based chromatography matrix with uniform size, a cross-flow microchannel chip was used to control the droplet size of cellulose solution and then the microdroplets were solidified to obtain the monodisperse cellulose beads. In the present work, ionic liquid, [EMIM] MP, was used to dissolve the microcrystalline cellulose as water phase and sunflower oil was used as oil phase. The effects of cellulose concentration, surfactant addition, flow rates of oil phase and water phase were investigated. The optimized preparation condition was 2% cellulose solution as water phase, flow rate of water phase of 6 μl · min-1 and flow rate of oil phase of 200 μl · min-1. The microdroplets of cellulose solution thus obtained could be about 100 μm with the variation coefficient less than 0. 2. After solidification and regeneration, cellulose beads were obtained with good sphericity. Wet density of beads was 1. 019 g · ml-1 , porosity was 94. 6%, and mean size was about 105.5 μm. The cellulose beads were coupled with DEAE ligand and used as weak anion-exchange resin. The ion exchange capacity was 123. 3 μmol

  12. Preparation of Waterborne Nanoscale Carbon Black Dispersion with Sodium Carboxymethyl Cellulose

    Institute of Scientific and Technical Information of China (English)

    YUAN Xia; FANG Kuan-jun

    2006-01-01

    Waterborne nanoscale carbon black dispersion (NCBD) was widely used in inkjet printing, spun-dyeing fibers and coloration fabrics. In this paper, NCBD was prepared using sodium carboxymethyl cellulose (CMC) as dispersant.Effects of CMC viscosity, ultrasonic time and oxidation with hydrogen peroxide on carbon black (CB) particle size were discussed. The results showed that CB particle size decreased by mechanical agitation while it increased by ultrasonic with the increase of CMC viscosity. Ultrasonic is a more effective method to disperse CB particles than that of mechanical agitation. CB particle size obviously decreased with increasing ultrasonic time and arrived at about 160 nm for 60 min. In addition, oxidation with 2 mol/L of H2O2 and 0.2 wt% of CMC300 reduced CB particle size to 160 nm at 90℃ for 2.5 h.

  13. Modified coaxial electrospinning for the preparation of high-quality ketoprofen-loaded cellulose acetate nanofibers.

    Science.gov (United States)

    Yu, Deng-Guang; Yu, Jia-Hui; Chen, Lan; Williams, Gareth R; Wang, Xia

    2012-10-01

    This study investigates the use of a modified coaxial electrospinning process in the production of drug-loaded cellulose acetate (CA) nanofibers. With CA employed as a filament-forming matrix and ketoprofen (KET) as an active pharmaceutical ingredient, modified coaxial processes using sheath fluids comprising only mixed solvents were undertaken. With a sheath-to-core flow rate ratio of 0.2:1, the nanofibers prepared from the coaxial process had a smaller average diameter, narrower size distribution, more uniform structures, and smoother surface morphologies than those generated from single fluid electrospinning. In addition, the coaxial fibers provided a better zero-order drug release profile. The use of a sheath solvent means that the core jet is subjected to electrical drawing for a longer period, facilitating homogeneous core jet solidification and retarding the formation of wrinkles on the surface of the nanofibers. This modified coaxial electrospinning protocol allows the systematic fabrication of functional polymer nanofibers with improved quality.

  14. Preparation and characterization of aminoethyl hydroxypropyl methyl cellulose modified with nisin.

    Science.gov (United States)

    Fan, Lihong; Hu, Jin; Hu, Zhihai; Peng, Min; Wen, Huigao; Li, Ya; Wang, Tan

    2016-08-01

    Nisin grafted aminoethyl hydroxypropyl methyl cellulose (AEHPMC) was prepared by an enzyme-catalyzed reaction in the presence of microbial transglutaminase (MTGase). AEHPMC was synthesized with 2-chloroethylamine hydrochloride (CEH) which was as an intermediate reactant. The parameters, which influenced the NH2% and the degree of substitution (DS), including reaction time, reaction temperature and the mass ratio of the reactants were investigated. Antioxidant activities of AEHPMC-nisin were evaluated by the scavenging activity of hydroxyl and 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical. With the DS and concentration increasing of AEHPMC-nisin, the radical scavenging activity increased. The Methylthiazol tetrazolium (MTT) assay indicated that AEHPMC-nisin had low-toxicity to L929 cells. Therefore, the derivative of HPMC may show a promising potential application in biomedical, food and pharmaceutical fields.

  15. Methods for the Selective Oxidation of Cellulose: Preparation of 2,3-Dicarboxycellulose and 6-Carboxycellulose

    NARCIS (Netherlands)

    Besemer, A.C.; Nooy, A.E.J. de; Bekkum, H. van

    1998-01-01

    Three methods for the selective oxidation of cellulose are described. The classical method consists of consecutive oxidation with sodium periodate, leading to 2,3-dialdehyde cellulose and sodium chlorite, giving 2,3-dicarboxy cellulose. This material, which is obtained in high yield and has a high

  16. Methods for the Selective Oxidation of Cellulose: Preparation of 2,3-Dicarboxycellulose and 6-Carboxycellulose

    NARCIS (Netherlands)

    Besemer, A.C.; Nooy, A.E.J. de; Bekkum, H. van

    1998-01-01

    Three methods for the selective oxidation of cellulose are described. The classical method consists of consecutive oxidation with sodium periodate, leading to 2,3-dialdehyde cellulose and sodium chlorite, giving 2,3-dicarboxy cellulose. This material, which is obtained in high yield and has a high c

  17. Chitosan-cellulose composite materials: Preparation, Characterization and application for removal of microcystin

    Energy Technology Data Exchange (ETDEWEB)

    Tran, Chieu D., E-mail: chieu.tran@marquette.edu [Department of Chemistry, Marquette University, P.O. Box 1881, Milwaukee, WI 53201 (United States); Duri, Simon [Department of Chemistry, Marquette University, P.O. Box 1881, Milwaukee, WI 53201 (United States); Delneri, Ambra; Franko, Mladen [Laboratory for Environmental Research, University of Nova Gorica, Vipavska 13, 5001 Nova Gorica (Slovenia)

    2013-05-15

    Highlights: •A novel and recyclable synthetic method using an ionic liquid, a Green Solvent. •Ecocomposite materials were synthesized from cellulose (CEL) and chitosan (CS). •Adding CEL into CS substantially increases tensile strength of the composite. •The composite is much better adsorbent for cyanotoxins than other materials. •The composite can be reused because adsorbed microcystin can be desorbed. -- Abstract: We developed a simple and one-step method to prepare biocompatible composites from cellulose (CEL) and chitosan (CS). [BMIm{sup +}Cl{sup −}], an ionic liquid (IL), was used as a green solvent to dissolve and prepare the [CEL + CS] composites. Since majority (>88%) of IL used was recovered for reuse by distilling the aqueous washings of [CEL + CS], the method is recyclable. XRD, FTIR, NIR, {sup 13}C CP-MAS-NMR and SEM were used to monitor the dissolution and to characterize the composites. The composite was found to have combined advantages of their components: superior mechanical strength (from CEL) and excellent adsorption capability for microcystin-LR, a deadly toxin produced by cyanobacteria (from CS). Specifically, the mechanical strength of the composites increased with CEL loading; e.g., up to 5× increase in tensile strength was achieved by adding 80% of CEL into CS. Kinetic results of adsorption confirm that unique properties of CS remain intact in the composite, i.e., it is not only a very good adsorbent for microcystin but also is better than all other available adsorbents. For example, it can adsorb 4× times more microcystin than the best reported adsorbent. Importantly, the microcystin adsorbed can be quantitatively desorbed to enable the composite to be reused with similar adsorption efficiency.

  18. Preparation of micro-fibrillated cellulose based on sugar palm ijuk (Arenga pinnata) fibres through partial acid hydrolysis

    Science.gov (United States)

    Saputro, A.; Verawati, I.; Ramahdita, G.; Chalid, M.

    2017-07-01

    The aim of this study was to isolate and characterized micro-fibrillated cellulose (MFC) from sugar palm/ijuk fibre (Arenga pinnata) by partial sulfuric acid hydrolysis. Cellulose fibre was prepared by repeated treatments with 5 wt% sodium hydroxide 2 h at 80°C, followed by bleaching with 1.7 wt% sodium chlorite for 2 h at 80°C in acidic environment under stirring. MFC was prepared by partial hydrolysis with sulfuric acid in various concentrations (30, 40, 50, and 60 % for 45 min at 45 °C) under stirring. Fourier Transform Infrared, Field Emission Scanning Electron Microscope, Thermo Gravimetric Analyzer and X-ray Diffraction characterized cellulose fibre and MFC. FTIR measurements showed that alkaline and bleaching treatments were effective to remove non-cellulosic constituents such as wax, lignin and hemicellulose. FESEM observation revealed conversion into more clear surface and defibrillation of cellulosic fibre after pre-treatments. XRD measurement revealed increase in crystallinity after pre-treatments and acid hydrolysis from 54.4 to 87.8%. Thermal analysis showed that increasing acid concentration reduced thermal stability.

  19. Enantioseparation Using Cellulose Tris(3,5-dimethylphenylcarbamate as Chiral Stationary Phase for HPLC: Influence of Molecular Weight of Cellulose

    Directory of Open Access Journals (Sweden)

    Yuji Okada

    2016-11-01

    Full Text Available The cellulose oligomers with different degrees of polymerization (DP, 7, 11, 18, 24, 26, 40 and 52, were prepared by hydrolysis of microcrystalline cellulose with phosphoric acid. These oligomers including the starting microcrystalline cellulose (DP 124 were converted to tris(3,5-dimethylphenylcarbamate (CDMPC derivatives by the reaction with an excess of 3,5-dimethylphenyl isocyanate to be used as the chiral stationary phase (CSP in high-performance liquid chromatography (HPLC. The structures of the CDMPC derivatives were investigated by infrared spectroscopy (IR, 1H-NMR, circular dichroism (CD and size exclusion chromatography (SEC, and the DPs of the derivatives estimated by SEC agreed with those estimated by 1H-NMR. After coating the derivatives on silica gel, their chiral recognition abilities were evaluated using eight racemates under a normal phase condition with a hexane-2-propanol (99/1 mixture as an eluent. The chiral recognition abilities of 7- and 11-mers, particularly the former, were lower than those of the higher oligomers from DP 18 to 52, which had rather similar abilities to that of 124-mer, although the abilities depended on the racemates. DP 18 seems to be sufficient for CDMPC to exhibit chiral recognition similar to that of the CDMPC with larger DPs.

  20. Nanocellulose prepared by acid hydrolysis of isolated cellulose from sugarcane bagasse

    Science.gov (United States)

    Wulandari, W. T.; Rochliadi, A.; Arcana, I. M.

    2016-02-01

    Cellulose in nanometer range or called by nano-cellulose has attracted much attention from researchers because of its unique properties. Nanocellulose can be obtained by acid hydrolysis of cellulose. The cellulose used in this study was isolated from sugarcane bagasse, and then it was hydrolyzed by 50% sulfuric acid at 40 °C for 10 minutes. Nanocellulose has been characterized by Transmission Electron Microscope (TEM), Particle Size Analyzer (PSA), Fourier Transform Infrared Spectroscopy (FTIR) and X-Ray Diffraction (XRD). Analysis of FTIR showed that there were not a new bond which formed during the hydrolysis process. Based on the TEM analysis, nano-cellulose has a spherical morphology with an average diameter of 111 nm and a maximum distribution of 95.9 nm determined by PSA. The XRD analysis showed that the crystallinity degree of nano-cellulose was higher than cellulose in the amount of 76.01%.

  1. Preparation and Characterization of Immobilized Lipase from Pseudomonas Cepacia onto Magnetic Cellulose Nanocrystals

    Science.gov (United States)

    Cao, Shi-Lin; Huang, Yu-Mei; Li, Xue-Hui; Xu, Pei; Wu, Hong; Li, Ning; Lou, Wen-Yong; Zong, Min-Hua

    2016-02-01

    Magnetic cellulose nanocrystals (MCNCs) were prepared and used as an enzyme support for immobilization of Pseudomonas cepacialipase (PCL). PCL was successfully immobilized onto MCNCs (PCL@MCNC) by a precipitation-cross-linking method. The resulting PCL@MCNC with a nanoscale size had high enzyme loading (82.2 mg enzyme/g) and activity recovery (95.9%). Compared with free PCL, PCL@MCNC exhibited significantly enhanced stability and solvent tolerance, due to the increase of enzyme structure rigidity. The observable optimum pH and temperature for PCL@MCNC were higher than those of free PCL. PCL@MCNC manifested relatively higher enzyme-substrate affinity and catalytic efficiency. Moreover, PCL@MCNC was capable of effectively catalyzing asymmetric hydrolysis of ketoprofenethyl ester with high yield of 43.4% and product e.e. of 83.5%. Besides, immobilization allowed PCL@MCNC reuse for at least 6 consecutive cycles retaining over 66% of its initial activity. PCL@MCNC was readily recycled by magnetic forces. Remarkably, the as-prepared nanobiocatalyst PCL@MCNC is promising for biocatalysis.

  2. Preparation of Pd/Bacterial Cellulose Hybrid Nanofibers for Dopamine Detection

    Directory of Open Access Journals (Sweden)

    Dawei Li

    2016-05-01

    Full Text Available Palladium nanoparticle-bacterial cellulose (PdBC hybrid nanofibers were synthesized by in-situ chemical reduction method. The obtained PdBC nanofibers were characterized by a series of analytical techniques. The results revealed that Pd nanoparticles were evenly dispersed on the surfaces of BC nanofibers. Then, the as-prepared PdBC nanofibers were mixed with laccase (Lac and Nafion to obtain mixture suspension, which was further modified on electrode surface to construct novel biosensing platform. Finally, the prepared electrochemical biosensor was employed to detect dopamine. The analysis result was satisfactory, the sensor showed excellent electrocatalysis towards dopamine with high sensitivity (38.4 µA·mM−1, low detection limit (1.26 µM, and wide linear range (5–167 µM. Moreover, the biosensor also showed good repeatability, reproducibility, selectivity and stability and was successfully used in the detection of dopamine in human urine, thus providing a promising method for dopamine analysis in clinical application.

  3. Biotemplated preparation of CdS nanoparticles/bacterial cellulose hybrid nanofibers for photocatalysis application.

    Science.gov (United States)

    Yang, Jiazhi; Yu, Junwei; Fan, Jun; Sun, Dongping; Tang, Weihua; Yang, Xuejie

    2011-05-15

    In this work, we describe a novel facile and effective strategy to prepare micrometer-long hybrid nanofibers by deposition of CdS nanoparticles onto the substrate of hydrated bacterial cellulose nanofibers (BCF). Hexagonal phase CdS nanocrystals were achieved via a simple hydrothermal reaction between CdCl(2) and thiourea at relatively low temperature. The prepared pristine BCF and the CdS/BCF hybrid nanofibers were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), UV-vis absorption spectroscopy (UV-vis), and X-ray photoelectron spectroscopy (XPS). The results reveal that the CdS nanoparticles were homogeneously deposited on the BCF surface and stabilized via coordination effect. The CdS/BCF hybrid nanofibers demonstrated high-efficiency photocatalysis with 82% methyl orange (MO) degradation after 90 min irradiation and good recyclability. The results indicate that the CdS/BCF hybrid nanofibers are promising candidate as robust visible light responsive photocatalysts.

  4. Synthesis and characterization of quaternized bacterial cellulose prepared in homogeneous aqueous solution.

    Science.gov (United States)

    Zhang, Hairong; Guo, Haijun; Wang, Bo; Shi, Silan; Xiong, Lian; Chen, Xinde

    2016-01-20

    In this work, bacterial cellulose (BC) was activated by ethylenediamine (EDA) and then dissolved in lithium chloride/N,N-dimethylacetamide (LiCl/DMAc) aqueous solutions. The resulting transparent solution was cast on a glass plate to prepare regenerated BC. Then cationic BC was prepared homogeneously by the reaction between regenerated BC and 3-chloro-2-hydroxypropyl-trimethyl ammonium chloride (CHPTAC) in a NaOH/urea aqueous solution. Structure and properties of the BC and its products were characterized by different techniques such as X-ray diffraction (XRD), Fourier transform spectroscopy (FT-IR), scanning electron microscopy (SEM) and thermo-gravimetric analysis (TGA). The results showed that there was no significant difference between the structures of BC, activated BC and regenerated BC. The effects of different temperature and molar ratio of CHPTAC to anhydroglucose unit (AGU) on the degree of substitution (DS) value were examined. The DS values of cationic BC ranged between 0.21 and 0.51.

  5. Conductive cable fibers with insulating surface prepared by co-axial electrospinning of multi-walled nanotubes and cellulose

    Science.gov (United States)

    Miyauchi, Minoru; Miao, Jianjun; Simmons, Trevor J.; Lee, Jong-Won; Doherty, Thomas V.; Dordick, Jonathan S.; Linhardt, Robert J.

    2010-01-01

    A core-sheath of multi-walled carbon nanotube (MWNT)-cellulose fibers of diameters from several hundreds nm to several µm were prepared by co-axial electrospinning from a non-valatile, non-flammable ionic liquid (IL) solvent, 1-methyl-3-methylimidazolium acetate ([EMIM][Ac]). MWNTs were dispersed in IL to form a gel solution. This gel core solution was electrospun surrounded by a sheath solution of cellulose disolved in the same IL. Electrospun fibers were collected in a coagulation bath containing ethanol-water to completely remove the IL and dried to form a core-sheath MWNT-cellulose fibers having a cable structure with a conductive core and insulating sheath. Enzymatic treatment of a portion of a mat of these fibers with cellulase selectively removed the cellulose sheath exposing the MWNT core for connection to an electrode. These MWNT-cellulose fiber mats demonstrated excellent conductivity due to a conductive pathway of bundleled MWNTs. Fiber mat conductivity increased with increasing ratio of MWNT in the fibers with a maximum conductivity of 10.7 S/m obtained at 45 wt% MWNT loading. PMID:20690644

  6. Tert-butyl alcohol used to fabricate nano-cellulose aerogels via freeze-drying technology

    Science.gov (United States)

    Wang, Xiaoyu; Zhang, Yang; Jiang, Hua; Song, Yuxuan; Zhou, Zhaobing; Zhao, Hua

    2017-06-01

    Aerogel, a highly porous material, is attracting increasing attention owing to low thermal conductivity and high specific surface area. Freeze-drying technology has been employed to produce nano-cellulose aerogels; however, the resultant product has low specific surface areas. Here, a modified approach to prepare nano-cellulose aerogels was reported, which involves tert-butyl alcohol as a solvent. Nano-cellulose aerogels were prepared via a spontaneous gelation fashion using calcium chloride solution, followed by tert-butyl alcohol solvent displacement and freeze drying. Addition of calcium chloride (0.25%) accelerated the physical gelation process. The application of tert-butyl alcohol as a solvent contributed to preservation of gel network. The obtained spherical nano-cellulose aerogels had a shrinkage rate of 5.89%. The specific surface area and average pore size was 164. 9666 m2 g-1 and 10.01 nm, respectively. Additionally, nano-cellulose aerogels had a comparable thermal degradation property when compared to microcrystalline cellulose. These biophysical properties make nano-cellulose aerogels as a promising absorption material.

  7. Device-quality Intrinsic Microcrystalline Silicon Prepared by 13.56MHz PECVD at High Pressure%高压13.56MHz PECVD法沉积器件质量级本征微晶硅材料

    Institute of Scientific and Technical Information of China (English)

    侯国付; 李以钢; 郭群超; 王岩; 薛俊明; 任慧志; 宋建; 张晓丹; 赵颖; 耿新华

    2005-01-01

    In this paper intrinsic hydrogenated microcrystalline silicon (μc-Si: H) thin films and solar cells prepared by radio-frequency plasma-enhanced chemical vapor deposition (RF-PECVD) method at high pressure are reported. Our experimental results demonstrated that either increasing plasma power or decreasing silane concentration always can lead to structural transition from amorphous silicon to microcrystalline silicon, and then the electrical properties changed along with the micro-structural evolution. By optimizing process parameters and using gas purifier, the oxygen concentration was prohibited effectively and then device-qualityμc-Si: H thin films have been got at a relative high deposition rate. Their applications as absorber layers in single-junctionμc-Si: H solar cells with 1.5μm i-layer yielded conversion efficiency of 5.22% without ZnO back reflector and without optimizing p-layer and p/i interface.%本文国内首次报道了采用高压RF-PECVD技术沉积本征微晶硅材料的结果.实验表明,增大等离子体激发功率和减小硅烷浓度都能够使薄膜材料由非晶硅逐渐向微晶硅转变,而结构上的改变使得电学特性也随之改变.通过工艺参数的优化和纯化器的使用,有效地控制了氧的掺杂,在较高的生长速度下得到了器件质量级的本征微晶硅材料.将实验得到的微晶硅作为太阳电池光吸收层,在没有ZnO背电极和没有优化窗口层材料以及p/i界面时,电池的效率达到5.22%,这进一步表明本征微晶硅材料的良好性能.

  8. Manufacture of cellulose nanocrystals by cation exchange resin-catalyzed hydrolysis of cellulose.

    Science.gov (United States)

    Tang, Li-rong; Huang, Biao; Ou, Wen; Chen, Xue-rong; Chen, Yan-dan

    2011-12-01

    Cellulose nanocrystals (CNC) were prepared from microcrystalline cellulose (MCC) by hydrolysis with cation exchange resin (NKC-9) or 64% sulfuric acid. The cation exchange resin hydrolysis parameters were optimized by using the Box-Behnken design and response surface methodology. An optimum yield (50.04%) was achieved at a ratio of resin to MCC (w/w) of 10, a temperature of 48 °C and a reaction time of 189 min. Electron microscopy (EM) showed that the diameter of CNCs was about 10-40 nm, and the length was 100-400 nm. Regular short rod-like CNCs were obtained by sulfuric acid hydrolysis, while long and thin crystals of cellulose were obtained with the cation exchange resin. X-ray diffraction (XRD) showed that, compared with MCC, the crystallinity of H2SO4-CNC and resin-CNC increased from 72.25% to 77.29% and 84.26%, respectively. The research shows that cation exchange resin-catalyzed hydrolysis of cellulose could be an excellent method for manufacturing of CNC in an environmental-friendly way. Copyright © 2011 Elsevier Ltd. All rights reserved.

  9. Optimized Monitoring of Production of Cellulose Nanowhiskers from Opuntia ficus-indica (Nopal Cactus

    Directory of Open Access Journals (Sweden)

    Horacio Vieyra

    2015-01-01

    Full Text Available Preparation of cellulose nanowhiskers (CNWs has grown significantly because they are useful for a wide range of applications. Additional advantage in their design requires that they meet the following characteristics: nontoxicity, abundance, sustainability, renewability, and low cost. To address these requirements, nanowhiskers were prepared from Opuntia ficus-indica (nopal cellulose by acid hydrolysis. Monitoring the process of CNWs preparation is necessary to ensure maximum yield and purity of the end product. In this study, the cellulose preparation was monitored by analyzing microscopic morphology by SEM; the purity degree was determined by fluorescence microscopy as a novel and rapid technique, and FTIR spectroscopy was used for confirmation. The additional parameters that monitored the process were the crystallinity index by X-ray diffraction and the size of the particle by dynamic light scattering (DLS. Nopal cellulose was found to be comparable to commercial microcrystalline cellulose. The use of Opuntia ficus-indica is a viable alternative for the production of highly pure CNWs and the strategy to supervise the preparation process was rapid.

  10. PREPARATION AND CHARACTERISTICS OF ANIONIC POLYACRYLAMIDES CONTAINING DIRECT DYE WITH A HIGH AFFINITY FOR CELLULOSE

    Directory of Open Access Journals (Sweden)

    Shingo Yokota

    2009-05-01

    Full Text Available Direct dye with a high affinity for cellulose substrate was utilized as a cellulose anchor to promote retention of paper strengthening additives under various conditions associated with the wet end of a paper machine. Direct Red 28 (DR was covalently linked to anionic polyacrylamide (A-PAM via a condensation reaction using water-soluble carbodiimide. The DR-conjugated A-PAM (DR-A-PAM demonstrated good retention efficiency, resulting in strength enhancement of handsheets. Anionic trash showed no interference with the performance of DR-A-PAM in the wet end, while the additive performance was sensitive to calcium ions. Surface plasmon resonance analysis gave useful information on the cellulose-anchoring ability of DR-A-PAM. Dye molecules were irreversibly adsorbed onto the cellulose substrate under aqueous conditions, while A-PAM possessed no significant affinity for cellulose. These results suggest that anionic DR moieties in DR-A-PAM molecules served as a cellulose-anchor, possibly due to multiple CH-π interaction between hydrophobic face of cellulose substrate and π-conjugated system of dye molecules. Such a unique interaction of direct dye and cellulose provides a new insight into the wet end system, and does not depend on conventional electrostatic attraction.

  11. Synthesis and properties of regenerated cellulose-based hydrogels with high strength and transparency for potential use as an ocular bandage

    Energy Technology Data Exchange (ETDEWEB)

    Patchan, M. [Research and Exploratory Development Department, The Johns Hopkins University Applied Physics Laboratory, 11100 Johns Hopkins Road, Laurel, MD 20723 (United States); Graham, J.L. [Department of Biomedical Engineering, Johns Hopkins University, School of Medicine, 720 Rutland Avenue/Ross 720, Baltimore, MD 21205 (United States); Xia, Z.; Maranchi, J.P. [Research and Exploratory Development Department, The Johns Hopkins University Applied Physics Laboratory, 11100 Johns Hopkins Road, Laurel, MD 20723 (United States); McCally, R. [Research and Exploratory Development Department, The Johns Hopkins University Applied Physics Laboratory, 11100 Johns Hopkins Road, Laurel, MD 20723 (United States); Wilmer Eye Institute, Johns Hopkins Medical Institutions, 600 N. Wolfe Street, Baltimore, MD 21287 (United States); Schein, O. [Wilmer Eye Institute, Johns Hopkins Medical Institutions, 600 N. Wolfe Street, Baltimore, MD 21287 (United States); Elisseeff, J.H. [Department of Biomedical Engineering, Johns Hopkins University, School of Medicine, 720 Rutland Avenue/Ross 720, Baltimore, MD 21205 (United States); Trexler, M.M., E-mail: morgana.trexler@jhuapl.edu [Research and Exploratory Development Department, The Johns Hopkins University Applied Physics Laboratory, 11100 Johns Hopkins Road, Laurel, MD 20723 (United States)

    2013-07-01

    Cellulose is a biologically derived material with excellent wound-healing properties. The high strength of cellulose fibers and the ability to synthesize gels with high optical transparency make these materials suitable for ocular applications. In this study, cellulose materials derived from wood pulp, cotton, and bacterial sources were dissolved in lithium chloride/N,N-dimethylacetamide to form regenerated cellulose hydrogels. Material properties of the resulting hydrogels, including water content, optical transparency, and tensile and tear strengths, were evaluated. Synthesis parameters, including activation time, dissolution time, relative humidity, and cellulose concentration, were found to impact the material properties of the resulting hydrogels. Overnight activation time improves the optical transparency of the hydrogels from 77% to 97% at 550 nm, whereas controlling cellulose concentration improves their tear strength by as much as 200%. On the basis of the measured transmittance and strength values of the regenerated hydrogels prepared via the optimized synthesis parameters, Avicel PH 101, Sigma-Aldrich microcrystalline cellulose 435236, and bacterial cellulose types were prioritized for future biocompatibility testing and potential clinical investigation. - Highlights: • Hydrogels were prepared (via LiCl/DMAc) from 7 different types of cellulose. • Synthesis parameters (activation, gelation, and concentration) were optimized. • Impact of synthesis parameters on transparency and strength was explored.

  12. Production of Starch Based Bioplastic from Cassava Peel Reinforced with Microcrystalline Celllulose Avicel PH101 Using Sorbitol as Plasticizer

    Science.gov (United States)

    Maulida; Siagian, M.; Tarigan, P.

    2016-04-01

    The production of starch based bioplastics from cassava peel reeinforced with microcrystalline cellulose using sorbitol as plasticizer were investigated. Physical properties of bioplastics were determined by density, water uptake, tensile strength and Fourier Transform Infrared Spectroscopy. Bioplastics were prepared from cassava peel starch plasticized using sorbitol with variation of 20; 25; 30% (wt/v of sorbitol to starch) reinforced with microcrystalline celllulose (MCC) Avicel PH101 fillers with range of 0 to 6% (wt/wt of MCC to starch). The results showed improvement in tensile strength with higher MCC content up to 9, 12 mpa compared to non-reinforced bioplastics. This could be mainly attributed to the strong hydrogen bonds between MCC and starch. On the contrary, the addition of MCC decreased the elongation at break, density and water uptake. Fourier Transform Infrared Spectroscopy showed the functional groups of bioplastics, which the majority of O-H groups were found at the bioplastics with reinforcing filler MCC that represented substantial hydrogen bonds. The highest tensile strength value was obtained for bioplastic with MCC content 6% and sorbitol content 20%. With good adhesion between MCC and starch the production of bioplastics could be widely used as a substitute for conventional plastics with more benefits to the environment.

  13. Preparation and characterization of nanoparticles of carboxymethyl cellulose acetate butyrate containing acyclovir

    Science.gov (United States)

    Vedula, Venkata Bharadwaz; Chopra, Maulick; Joseph, Emil; Mazumder, Sonal

    2016-02-01

    Nanoparticles of carboxymethyl cellulose acetate butyrate complexed with the poorly soluble antiviral drug acyclovir (ACV) were produced by precipitation process and the formulation process and properties of nanoparticles were investigated. Two different particle synthesis methods were explored—a conventional precipitation method and a rapid precipitation in a multi-inlet vortex mixer. The particles were processed by rotavap followed by freeze-drying. Particle diameters as measured by dynamic light scattering were dependent on the synthesis method used. The conventional precipitation method did not show desired particle size distribution, whereas particles prepared by the mixer showed well-defined particle size ~125-450 nm before and after freeze-drying, respectively, with narrow polydispersity indices. Fourier transform infrared spectroscopy showed chemical stability and intactness of entrapped drug in the nanoparticles. Differential scanning calorimetry showed that the drug was in amorphous state in the polymer matrix. ACV drug loading was around 10 wt%. The release studies showed increase in solution concentration of drug from the nanoparticles compared to the as-received crystalline drug.

  14. Preparation and Characterization of Blended Films from Quaternized Hemicelluloses and Carboxymethyl Cellulose

    Directory of Open Access Journals (Sweden)

    Xian-Ming Qi

    2015-12-01

    Full Text Available Utilization of hemicelluloses from biomass energy is an important approach to explore renewable resources. A convenient, quick, and inexpensive method for the preparation of blended films from quaternized hemicelluloses (QH and carboxymethyl cellulose (CMC was introduced into this study. QH and CMC solution were first mixed to form homogeneous suspension, and then were dried under vacuum to fabricate the blended films. The FT-IR and XRD results indicated that the linkage between QH and CMC was due to the hydrogen bonding and electrostatic interaction. From the results of mechanical properties and water vapor permeability (WVP, the tensile strength of the blended films increased with the QH/CMC content ratio increasing in appropriate range, and the WVP of the blended films decreased. The maximum value of tensile strength of blend film achieved was 27.4 MPa. In addition, the transmittances of the blended films increased with the decreasing of QH/CMC content ratio. When the weight ratio (QH: CMC was 1:1.5, the blend film showed the best light transmittance (45%. All the results suggested that the blended films could be used in areas of application in the coating and packaging fields from the good tensile strength, transmittance, and low WVP.

  15. Preparation and characterization of a bacterial cellulose/silk fibroin sponge scaffold for tissue regeneration.

    Science.gov (United States)

    Oliveira Barud, H G; Barud, Hernane da S; Cavicchioli, Maurício; do Amaral, Thais Silva; de Oliveira Junior, Osmir Batista; Santos, Diego M; Petersen, Antonio Luis de Oliveira Almeida; Celes, Fabiana; Borges, Valéria Matos; de Oliveira, Camila I; de Oliveira, Pollyanna Francielli; Furtado, Ricardo Andrade; Tavares, Denise Crispim; Ribeiro, Sidney J L

    2015-09-05

    Bacterial cellulose (BC) and silk fibroin (SF) are natural biopolymers successfully applied in tissue engineering and biomedical fields. In this work nanocomposites based on BC and SF were prepared and characterized by scanning electron microscopy (SEM), infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). In addition, the investigation of cytocompatibility was done by MTT, XTT and Trypan Blue dye technique. Cellular adhesion and proliferation were detected additionally. The evaluation of genotoxicity was realized by micronucleus assay. In vitro tests showed that the material is non-cytotoxic or genotoxic. SEM images revealed a greater number of cells attached at the BC/SF:50% scaffold surface than the pure BC one, suggesting that the presence of fibroin improved cell attachment. This could be related to the SF amino acid sequence that acts as cell receptors facilitating cell adhesion and growth. Consequently, BC/SF:50% scaffolds configured an excellent option in bioengineering depicting its potential for tissue regeneration and cultivation of cells on nanocomposites.

  16. Preparation and properties of environmental-friendly coatings based on carboxymethyl cellulose nitrate ester & modified alkyd.

    Science.gov (United States)

    Duan, Hongtao; Shao, Ziqiang; Zhao, Ming; Zhou, Zhenwen

    2016-02-10

    Amphipathic coating basic film-forming material carboxymethyl cellulose nitrate ester (CMCN) was synthesized and characterizations of CMCN with different ratio of functional groups were studied. Ratios of functional groups on each repeating units of CMCN have great importance in the decision of CMCN properties using as an amphipathic coating basic film-forming material and ratios of functional groups were the most concerned of the study. Ratios of functional groups on each repeating units of CMCN were measured by elemental analyzer and calculated. Series of experiments were conducted using different ratios of functional groups of CMCN. Thermal properties of CMCN were measured by FT-IR and TG. Densities of CMCN powders were measured. Aqueous coatings based on CMCN/alkyd (after chemical modified by coconut oil) were prepared and morphology & rheology of CMCN hydrophilic dispersions were measured using an Anton-Paar-Strasse 20A-8054 Graz analyzer. Contact angles between films based on CMCN and deionized water were recorded. Other properties of films were measured. CMCN with the etherification of carboxymethyl groups at 0.35-0.40, nitrate ester groups at 1.96-2.19 and hydroxyl groups at 0.46-0.64 per d-glucose was considered as the best film forming material.

  17. PREPARATION AND PROPERTIES OF ETHYL-CYANOETHYL CELLULOSE/POLYACRYLIC ACID COMPOSITE FILMS WITH REFLECTION COLORS

    Institute of Scientific and Technical Information of China (English)

    Yong Huang

    2001-01-01

    Ethyl-cyanoethyl cellulose [(E-CE)C]/acrylic acid (AA) becomes a cholesteric liquid crystalline solution with vivid colors when the (E-CE)C concentration is 42 wt% ~52 wt%. (E-CE)C/polyacrylic acid (PAA) composites with cholesteric structure were prepared by polymerizing AA in (E-CE)C/AA liquid crystalline solutions. The layers of ordered polymer chains in the cholesteric phase were inclined during polymerization and the degree of the inclination depended on the polymerization temperature and the concentration of the solution before polymerization. The cholesteric structure in the composites could not be changed when temperature was lower than 100C. Cross-linking of the PAA in composites improved their water-resistance. The cholesteric order of the composites without cross-linking was destroyed when they where immersed in water. The color derived from the selective reflection of the cholesteric phase of the cross-linked composites turned from blue to red after the composites absorbed water. The color of the composites could be returned to the original one when the absorbed water was removed from the swollen composites.

  18. Nanostructured zirconium titanate fibers prepared by particulate sol–gel and cellulose templating techniques

    Energy Technology Data Exchange (ETDEWEB)

    Rouhani, P. [Helmerich Advanced Technology Research Center, School of Electrical and Computer Engineering, Oklahoma State University, OK 74106 (United States); Salahinejad, E. [Helmerich Advanced Technology Research Center, School of Material Science and Engineering, Oklahoma State University, OK 74106 (United States); Department of Materials Science and Engineering, School of Engineering, Shiraz University, Zand Blvd., 7134851154 Shiraz (Iran, Islamic Republic of); Kaul, R. [Department of Biochemistry and Microbiology, Center for Health Sciences, Oklahoma State University, OK 74107 (United States); Vashaee, D. [Helmerich Advanced Technology Research Center, School of Electrical and Computer Engineering, Oklahoma State University, OK 74106 (United States); Tayebi, L., E-mail: lobat.tayebi@okstate.edu [Helmerich Advanced Technology Research Center, School of Material Science and Engineering, Oklahoma State University, OK 74106 (United States); School of Chemical Engineering, Oklahoma State University, Stillwater, OK 74078 (United States)

    2013-08-15

    Highlights: •A method to produce zirconium titanate fibers was introduced. •The resultant structure and photocatalytic activity of the fiber were investigated. •The fiber exhibited higher photocatalytic characteristics, compared with the powders. -- Abstract: In this paper, a method for cost-effective production of nanostructured zirconium titanate (ZrTiO{sub 4}) fibers is introduced. In this method, ZrTiO{sub 4} fibers were synthesized by a sol–gel technique using cellulose fibers as the template. The resultant structures were studied by transmission electron microscopy, X-ray diffraction, scanning electron microscopy, and Brunauer–Emmett–Teller (BET) analyses. The photocatalytic activity of the fiber was compared to that of ZrTiO{sub 4} powders prepared by the same sol–gel method, in dark and under UVA and UVC radiations. According to the results, after calcination accompanied by the template removal, the ZrTiO{sub 4} fiber consists of uniformly-deposited, crystalline nanoparticles. This nanostructured fiber exhibited a higher surface area and a higher porosity compared with the ZrTiO{sub 4} powders, resulting in considerably higher photocatalytic characteristics, as confirmed by the experiment. The large surface area and the enhanced photocatalytic activity of the ZrTiO{sub 4} fibers also offer applications in sensors and bioactive films.

  19. The role of cellulose nanocrystals incorporation route in waterborne polyurethane for preparation of electrospun nanocomposites mats.

    Science.gov (United States)

    Santamaria-Echart, Arantzazu; Ugarte, Lorena; Gonzalez, Kizkitza; Martin, Loli; Irusta, Lourdes; Gonzalez, Alba; Corcuera, Maria Angeles; Eceiza, Arantxa

    2017-06-15

    Electrospinning offers the possibility of obtaining fibers mats from polymer solutions. The use of environmentally-friendly waterborne polyurethane (WBPU) allows obtaining electrospun polyurethane mats in water medium. Furthermore, the incorporation of water dispersible nanoentities, like renewable cellulose nanocrystals (CNC), is facilitated. Therefore, in this work, a WBPU was synthesized and CNC were isolated for preparing WBPU-CNC dispersions nanocomposites with 1 and 3wt% of CNC following both the classical mixing by sonication, and the innovative in-situ route. The dispersions were used for obtaining electrospun mats assisted by poly(ethylene oxide) (PEO) as polymer template. Moreover, the extraction of PEO with water resulted in continuous WBPU-CNC mats, showing different properties respect to WBPU-CNC mats containing PEO. The effective addition of CNC led to more defined cylindrical morphologies and the two alternative incorporation routes induced to different CNC dispositions in the matrix, which modified fibers diameters, and thus, mats final properties. Copyright © 2017 Elsevier Ltd. All rights reserved.

  20. Surface and Adsorption Properties of Activated Carbon Fabric Prepared from Cellulosic Polymer: Mixed Activation Method

    Energy Technology Data Exchange (ETDEWEB)

    Bhati, Surendra; Mahur, J. S.; Choubey, O. N. [Barkatullah Univ., Bhopal (India); Dixit, Mahur Savita [Maulana Azad National Institute of Technology, Bhopla (India)

    2013-02-15

    In this study, activated carbon fabric was prepared from a cellulose-based polymer (viscose rayon) via a combination of physical and chemical activation (mixed activation) processes by means of CO{sub 2} as a gasifying agent and surface and adsorption properties were evaluated. Experiments were performed to investigate the consequence of activation temperature (750, 800, 850 and 925 .deg. C), activation time (15, 30, 45 and 60 minutes) and CO{sub 2} flow rate (100, 200, 300 and 400 mL/min) on the surface and adsorption properties of ACF. The nitrogen adsorption isotherm at 77 K was measured and used for the determination of surface area, total pore volume, micropore volume, mesopore volume and pore size distribution using BET, t-plot, DR, BJH and DFT methods, respectively. It was observed that BET surface area and TPV increase with rising activation temperature and time due to the formation of new pores and the alteration of micropores into mesopores. It was also found that activation temperature dominantly affects the surface properties of ACF. The adsorption of iodine and CCl{sub 4} onto ACF was investigated and both were found to correlate with surface area.

  1. Preparation and Characterization of Polymeric Surfactants Based on Epoxidized Soybean Oil Grafted Hydroxyethyl Cellulose.

    Science.gov (United States)

    Huang, Xujuan; Liu, He; Shang, Shibin; Rao, Xiaoping; Song, Jie

    2015-10-21

    Epoxidized soybean oil (ESO) grafted hydroxyethyl cellulose (HEC) was prepared via ring-opening polymerization, in which the hydroxyl groups of HEC acted as initiators and the polymeric ESO were covalently bonded to the HEC. Hydrolysis of ESO-grafted HEC (ESO-HEC) was performed with sodium hydroxide, and the hydrolyzed ESO-HEC (H-ESO-HEC) products were characterized via Fourier transform infrared (FT-IR) and (1)H and (13)C nuclear magnetic resonance (NMR) spectroscopies, high-temperature gel permeation chromatography (HT-GPC), and differential scanning calorimetry (DSC). The results indicated that ring-opening polymerization of ESO occurred with the hydroxyl groups of HEC as initiators. The molecular weights of the H-ESO-HEC products were varied by adjusting the mass ratio of HEC and ESO. Through neutralizing the carboxylic acid of H-ESO-HEC with sodium hydroxide, novel polymeric surfactants (H-ESO-HEC-Na) were obtained, and the effects of polymeric surfactants on the surface tension of water were investigated as a function of concentration of H-ESO-HEC-Na. The H-ESO-HEC-Na was effective at lowering the surface tension of water to 26.33 mN/m, and the critical micelle concentration (CMC) value decreased from 1.053 to 0.157 g/L with increases in molecular weights of the polymeric surfactants. Rheological measurements indicated that the H-ESO-HEC-Na solutions changed from pseudoplastic property to Newtonian with increasing shear rate.

  2. Two-Sided Surface Oxidized Cellulose Membranes Modified with PEI: Preparation, Characterization and Application for Dyes Removal

    OpenAIRE

    Wei Wang; Qian Bai; Tao Liang; Huiyu Bai; Xiaoya Liu

    2017-01-01

    Porous regenerated cellulose (RC) membranes were prepared with cotton linter pulp as a raw material. These membranes were first oxidized on both sides by a modified (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) oxidation system using a controlled oxidation reaction technique. Then, the oxidized RC membranes were functionalized with polyethylenimine (PEI) via the glutaraldehyde crosslinking method to obtain bifunctional (carboxyl and amino) porous RC membranes, as revealed by Fourier transfo...

  3. Poly(hydroxybutyrate)/cellulose acetate blend nanofiber scaffolds: Preparation, characterization and cytocompatibility

    Energy Technology Data Exchange (ETDEWEB)

    Zhijiang, Cai, E-mail: caizhijiang@hotmail.com [School of Textiles, Tianjin Polytechnic University, Tianjin 300387 (China); State Key Laboratory of Hollow Fiber Membrane Material and Processes, No 399 BingShuiXi Street, XiQing District, Tianjin, China, 300387 (China); Yi, Xu; Haizheng, Yang; Jia, Jianru; Liu, Yuanpei [School of Textiles, Tianjin Polytechnic University, Tianjin 300387 (China)

    2016-01-01

    Poly(hydroxybutyrate) (PHB)/cellulose acetate (CA) blend nanofiber scaffolds were fabricated by electrospinning using the blends of chloroform and DMF as solvent. The blend nanofiber scaffolds were characterized by SEM, FTIR, XRD, DSC, contact angle and tensile test. The blend nanofibers exhibited cylindrical, uniform, bead-free and random orientation with the diameter ranged from 80–680 nm. The scaffolds had very well interconnected porous fibrous network structure and large aspect surface areas. It was found that the presence of CA affected the crystallization of PHB due to formation of intermolecular hydrogen bonds, which restricted the preferential orientation of PHB molecules. The DSC result showed that the PHB and CA were miscible in the blend nanofiber. An increase in the glass transition temperature was observed with increasing CA content. Additionally, the mechanical properties of blend nanofiber scaffolds were largely influenced by the weight ratio of PHB/CA. The tensile strength, yield strength and elongation at break of the blend nanofiber scaffolds increased from 3.3 ± 0.35 MPa, 2.8 ± 0.26 MPa, and 8 ± 0.77% to 5.05 ± 0.52 MPa, 4.6 ± 0.82 MPa, and 17.6 ± 1.24% by increasing PHB content from 60% to 90%, respectively. The water contact angle of blend nanofiber scaffolds decreased about 50% from 112 ± 2.1° to 60 ± 0.75°. The biodegradability was evaluated by in vitro degradation test and the results revealed that the blend nanofiber scaffolds showed much higher degradation rates than the neat PHB. The cytocompatibility of the blend nanofiber scaffolds was preliminarily evaluated by cell adhesion studies. The cells incubated with PHB/CA blend nanofiber scaffold for 48 h were capable of forming cell adhesion and proliferation. It showed much better biocompatibility than pure PHB film. Thus, the prepared PHB/CA blend nanofiber scaffolds are bioactive and may be more suitable for cell proliferation suggesting that these scaffolds can be used for

  4. Fermentative hydrogen production from hydrolyzed cellulosic feedstock prepared with a thermophilic anaerobic bacterial isolate

    Energy Technology Data Exchange (ETDEWEB)

    Lo, Yung Chung [Department of Chemical Engineering, National Cheng Kung University, No. 1 University Road, Tainan 701 (China); Huang, Chi-Yu.; Fu, Tzu-Ning [Department of Environmental Engineering and Science, Tunghai University, Taichung 407 (China); Chen, Chun-Yen; Chang, Jo-Shu [Department of Chemical Engineering, National Cheng Kung University, No. 1 University Road, Tainan 701 (China); Sustainable Environment Research Center, National Cheng Kung University, Tainan (China)

    2009-08-15

    Hydrogen gas was produced via dark fermentation from natural cellulosic materials and {alpha}-cellulose via a two-step process, in which the cellulosic substrates were first hydrolyzed by an isolated cellulolytic bacterium Clostridium strain TCW1, and the resulting hydrolysates were then used as substrate for fermentative H{sub 2} production. The TCW1 strain was able to hydrolyze all the cellulosic materials examined to produce reducing sugars (RS), attaining the best reducing sugar production yield of 0.65 g reducing sugar/g substrate from hydrolysis of {alpha}-cellulose. The hydrolysates of those cellulosic materials were successfully converted to H{sub 2} via dark fermentation using seven H{sub 2}-producing bacterial isolates. The bioH{sub 2} production performance was highly dependent on the type of cellulosic feedstock used, the initial reducing sugar concentration (C{sub RS,o}) (ranging from 0.7 to 4.5 mg/l), as well as the composition of sugar and soluble metabolites present in the cellulosic hydrolysates. It was found that Clostridium butyricum CGS5 displayed the highest H{sub 2}-producing efficiency with a cumulative H{sub 2} production of 270 ml/l from {alpha}-cellulose hydrolysate (C{sub RS,o} = 4.52 mg/l) and a H{sub 2} yield of 7.40 mmol/g RS (or 6.66 mmol/g substrate) from napier grass hydrolysate (C{sub RS,o} = 1.22 g/l). (author)

  5. Preparation of CeO2 Nanoparticles and Its Application to Ion-selective Electrodes Based on Acetyl Cellulose

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    CeO2 nanoparticles with an average diameter of about 30 nm were prepared by sol-gel method at lower temperature. The gel, transformed from the aqueous solution of metal nitrate and citric acid, can be combusted completely at lower temperature. The redox behavior and the crystallization process of the dried gel were studied by thermogravimetric analysis and infrared spectroscopy. The synthesized powders were characterized by X-ray powder diffraction and transmission electron microscopy. In addition, rare earth elements ion-selective electrodes based on acetyl cellulose were prepared using ultra fine cerium oxide powders.

  6. Preparation and Evaluation of a Novel Cellulose Tris(N-3,5-dimethylphenylcarbamate) Chiral Stationary Phase

    Institute of Scientific and Technical Information of China (English)

    GE,Jin; ZHAO,Liang; SHI,Yan-Ping

    2008-01-01

    A novel cellulose tris(N-3,5-dimethylphenylcarbamate) (CDMPC) chiral stationary phase (CSP) was prepared by coating CDMPC on TiO2/SiO2, which was prepared by coating titania nanoparticles on silica through a self-assemble technique. At first, 2-hydroxyl-phenyl acetonitrile and α-phenylethanol were separated on this new CSP to evaluate the chiral separation ability. Then, two pesticides, matalaxyl and diclofop-methyl were separated.The influence of the mobile phase composition on the enantioselectivity was discussed, and the repeatability and stability of the CSP were studied too.

  7. Cellulose whiskers: preparation, characterization and surface modification; Whiskers de celulose: preparacao, caracterizacao e modificacao de superficie

    Energy Technology Data Exchange (ETDEWEB)

    Taipina, Marcia O.; Ferrarezi, Marcia M.F.; Goncalves, Maria C., E-mail: maria@iqm.unicamp.br [Instituto de Quimica, Universidade Estadual de Campinas, Campinas, SP (Brazil)

    2011-07-01

    The main objectives of this work were to produce cellulose whiskers (from cotton fibers) by acid hydrolysis and subsequently modify the surface of these whiskers with 3-iso-cyanate-propyltrietoxy-silane. Cellulose whiskers structures were characterized by X-ray diffraction and Fourier transform infrared and their morphologies were investigated by scanning and transmission electron microscopy. Due to the hydrophilic nature of native cellulose, the formation of cellulose whisker nanocomposites is limited to water-soluble polymers. The applied methodology for surface modification of the whiskers allowed to obtain nanofibers with surface features more appropriate to allow the adhesion at fiber-matrix interface, which may result in a better performance of these fibers as reinforcing agents of hydrophobic polymer matrices. (author)

  8. Preparation and properties of biodegradable films from Sterculia urens short fiber/cellulose green composites.

    Science.gov (United States)

    Jayaramudu, J; Reddy, G Siva Mohan; Varaprasad, K; Sadiku, E R; Sinha Ray, S; Varada Rajulu, A

    2013-04-02

    The development of commercially viable "green products", based on natural resources for the matrices and reinforcements, in a wide range of applications, is on the rise. The present paper focuses on Sterculia urens short fiber reinforced pure cellulose matrix composite films. The morphologies of the untreated and 5% NaOH (alkali) treated S. urens fibers were observed by SEM. The effect of 5% NaOH treated S. urens fiber (5, 10, 15 and 20% loading) on the mechanical properties and thermal stability of the composites films is discussed. This paper presents the developments made in the area of biodegradable S. urens short fiber/cellulose (SUSF/cellulose) composite films, buried in the soil and later investigated by the (POM), before and after biodegradation has taken place. SUSF/cellulose composite films have great potential in food packaging and for medical applications. Copyright © 2013 Elsevier Ltd. All rights reserved.

  9. Preparation of cellulose-based sponges for wound dressing and healing

    OpenAIRE

    2013-01-01

    For healing of chronic or burn wounds, polymeric sponges have been recently applied. Due to a high absorption capacity, noncitotoxicity and good swelling capabilities, for their production natural polymers are often used. In this study, macroporous regenerated cellulose was evaluated as a matrix for wound dressing materials. Active compounds, such as antibiotic neomycin and phenolic compound quercetin were immobilized in the cellulosic matrix aimed to promote wound healing process. Active com...

  10. Preparation of native cellulose-AgCl fiber with antimicrobial activity through one-step electrospinning.

    Science.gov (United States)

    Wang, Shaojun; Zhang, Xiaomin; Luo, Ting; Zhu, Jin; Su, Shengpei

    2017-02-01

    The native Cellulose-AgCl fiber have been firstly fabricated by one-step electrospinning of cellulose solution with poly(vinyl pyrrolidone) (PVP) and AgNO3. X-ray diffraction, Scanning electron microscopy (SEM), Energy dispersive spectrometer, Thermo-gravimetric analysis and Fourier transform infrared are used to characterize the crystal structure, morphology and composition of cellulose-AgCl nanocomposites. The results of SEM indicate that the size of AgCl in cellulose fiber matrix is able to be adjusted by the addition of Polyvinylpyrrolidone (PVP). The antimicrobial activity of the nanocomposites fiber is also tested against the model microbes E. coli (Gram-negative) and S. aureus (Gram-positive). The results indicate that cellulose-AgCl nanocomposites have a good antimicrobial activity, which is improving with the decrease of AgCl size in fiber matrix. This work provides a novel and simple way to adjust the AgCl size in electrospinning cellulose matrix which can be applied as functional biomaterials.

  11. Response Surface Methodology for the Optimization of Preparation of Biocomposites Based on Poly(lactic acid and Durian Peel Cellulose

    Directory of Open Access Journals (Sweden)

    Patpen Penjumras

    2015-01-01

    Full Text Available Response surface methodology was used to optimize preparation of biocomposites based on poly(lactic acid and durian peel cellulose. The effects of cellulose loading, mixing temperature, and mixing time on tensile strength and impact strength were investigated. A central composite design was employed to determine the optimum preparation condition of the biocomposites to obtain the highest tensile strength and impact strength. A second-order polynomial model was developed for predicting the tensile strength and impact strength based on the composite design. It was found that composites were best fit by a quadratic regression model with high coefficient of determination (R2 value. The selected optimum condition was 35 wt.% cellulose loading at 165°C and 15 min of mixing, leading to a desirability of 94.6%. Under the optimum condition, the tensile strength and impact strength of the biocomposites were 46.207 MPa and 2.931 kJ/m2, respectively.

  12. The Influence of Casting Machine Speed in Cellulose Acetate Membrane Preparation

    Directory of Open Access Journals (Sweden)

    Luqman Buchori

    2010-12-01

    Full Text Available Membranes are being increasingly used as a valuable separation tool in laboratory as well as in industrial processes.  Continual  development  of  new  membrane  materials  is  crucial  to  sustain  and  expand  the growing  interest  in  this  technology  and  modern  polymer  chemistry  is  highly  proficient  in  tailoring polymers with desired properties such as increased mechanical, thermal and chemical stability. Cellulose acetate (CA is one of the membrane polymers that has been used for aqueous based separation and used as both reverses osmosis (RO and ultrafiltration (UF membranes.   This paper presents investigation of influence of casting machine speed in membrane preparation. CA is used in this study. That was CA-398-30 with average  acetyl  content  39.8 wt %.  Non solvent  used is water  and the  solvent  is 99.7 %  organic Dimethyl Sulfoxide  (DMSO. The homogenous CA/DMSO  solutions were prepared by dissolving CA  in DMSO solvent. The CA concentration were varied 13 and 16 % while casting solution speed were varied from  20  to  80  mm/sec  with  distance  cutting  machine  were  fixed  at  14  cm.  In  addition,  non  solvent  in coagulation  bath  also  were  varied  by  100  %  water  and  10  %  DMSO  in  water.  The results  of  this experiment   describe   effect   of   casting   machine   speed   to   water   permeability.   The   effect   of   CA concentration  to  water  permeability  shows the  adversative result  between 13 and  16 %  CA  in  100 non solvent water. The similar result also observed in 10 % DMSO in water.

  13. Carbon-supported base metal nanoparticles : Cellulose at work

    NARCIS (Netherlands)

    Hoekstra, Jacco; Versluijs-Helder, Marjan; Vlietstra, Edward J.; Geus, John W.; Jenneskens, Leonardus W.

    2015-01-01

    Pyrolysis of base metal salt loaded microcrystalline cellulose spheres gives a facile access to carbon-supported base metal nanoparticles, which have been characterized with temperature-dependent XRD, SEM, TEM, ICP-MS and elemental analysis. The role of cellulose is multifaceted: 1) it facilitates a

  14. A Study on Properties of Microcrystalline Glass Prepared from Iron Tailing%铁尾矿微晶玻璃的制备及其性能研究

    Institute of Scientific and Technical Information of China (English)

    韩茜; 张洋

    2015-01-01

    The iron tailing of Liangshuigou,Danfeng Country,Shangluo City, is used as the main raw material to prepare the micro crystalline glass. The XRD phase analysis, density, Moh's hardness, compressive strength and corrosion resistance of the samples is tested. The influence of different sintering temperature on the properties of samples is analyzed. The results show that with the sintering temperature rising, the density, Moh's hardness, compressive strength and corrosion resistance of the samples are increasing firstly and then decreasing. When the sintering temperature at 1150℃, the properties of samples are the best. The density is 2.84 g·cm-3, Moh's hardness range of 5.5-6.5, compressive strength is 132 . 25 MPa , weight loss in acid rate is 0 . 016%, alkaline weight loss rate is 0 . 121%. Therefore, for the better properties, the best sintering temperature of this tailing is 1150℃.%以商洛市丹凤县梁水沟铁尾矿为主要原料来制备微晶玻璃,通过测试样品的XRD图谱、密度、莫氏硬度、抗压强度和耐腐蚀性能,来分析不同烧结温度对样品性能的影响。实验结果表明:随着烧结温度的升高,试样的密度、莫氏硬度及抗压强度均先增大后减小,失重率先减小后增大。在1150℃烧结时,各项性能均最好,密度为2.84 g·cm-3,莫氏硬度为5.5-6.5,抗压强度达132.25 MPa,酸性失重率为0.016%,碱性失重率为0.121%。因此,为了获得较好的性能,此类尾矿的最佳烧结温度为1150℃。

  15. Processive endoglucanase active in crystalline cellulose hydrolysis by the brown rot Basidiomycete Gloeophyllum trabeum

    Science.gov (United States)

    Roni Cohen; Melissa R. Suzuki; Kenneth E. Hammel

    2005-01-01

    Brown rot basidiomycetes have long been thought to lack the processive cellulases that release soluble sugars from crystalline cellulose. On the other hand, these fungi remove all of the cellulose, both crystalline and amorphous, from wood when they degrade it. To resolve this discrepancy, we grew Gloeophyllum trabeum on microcrystalline cellulose (Avicel) and purified...

  16. A facile approach to prepare regenerated cellulose/graphene nanoplatelets nanocomposite using room-temperature ionic liquid.

    Science.gov (United States)

    Mahmoudian, Shaya; Wahit, Mat Uzir; Imran, Muhammad; Ismail, A F; Balakrishnan, Harintharavimal

    2012-07-01

    This study presents the preparation of regenerated cellulose (RC)/graphene nanoplatelets (GNPs) nanocomposites via room temperature ionic liquid, 1-ethyl-3-methylimidazolium acetate (EMIMAc) using solution casting method. The thermal stability, gas permeability, water absorption and mechanical properties of the films were studied. The synthesized nanocomposite films were characterized by Fourier transform infrared (FTIR), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The T20 decomposition temperature of regenerated cellulose improved with the addition of graphene nanoplatelets up to 5 wt%. The tensile strength and Young's modulus of RC films improved by 34 and 56%, respectively with the addition of 3 wt% GNPs. The nanocomposite films exhibited improved oxygen and carbon dioxide gas barrier properties and water absorption resistance compared to RC. XRD and SEM results showed good interaction between RC and GNPs and well dispersion of graphene nanoplatelets in regenerated cellulose. The FTIR spectra showed that the addition of GNPs in RC did not result in any noticeable change in its chemical structure.

  17. Novel Cu@SiO{sub 2}/bacterial cellulose nanofibers: Preparation and excellent performance in antibacterial activity

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Bo [Chemicobiology and Functional Materials Institute of Nanjing University of Science and Technology, Xiao Ling Wei 200, Nanjing 210094 (China); Department of Life Sciences of Lianyungang Teacher' s College, Sheng Hu Lu 28, Lianyungang 222006 (China); Huang, Yang; Zhu, Chunlin; Chen, Chuntao; Chen, Xiao; Fan, Mengmeng [Chemicobiology and Functional Materials Institute of Nanjing University of Science and Technology, Xiao Ling Wei 200, Nanjing 210094 (China); Sun, Dongping, E-mail: sundpe301@163.com [Chemicobiology and Functional Materials Institute of Nanjing University of Science and Technology, Xiao Ling Wei 200, Nanjing 210094 (China)

    2016-05-01

    The antibacterial composite based on bacterial cellulose (BC) was successfully prepared by in-situ synthesis of SiO{sub 2} coated Cu nanoparticles (Cu@SiO{sub 2}/BC) and its properties were characterized. Its chemical structures and morphologies were evaluated by Fourier transformation infrared spectrum (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The results demonstrated that the SiO{sub 2} coated Cu particles were well homogeneously precipitated on the surface of BC. The Cu@SiO{sub 2}/BC was more resistant to oxidation than the Cu nanoparticles impregnated into BC (Cu/BC) and then Cu@SiO{sub 2}/BC could prolong the antimicrobial activity against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli). - Graphical abstract: Schematic illustration of the preparation of Cu@SiO{sub 2}/BC. Due to its unique structure, the Cu@SiO{sub 2}/BC membrane shows excellent antibacterial effects and can be used for a long time. - Highlights: • This work paves the novel way to fabricate antibacterial nanomaterial with good efficiency. • We prepare the antibacterial membrane based on bacterial cellulose by in-situ synthesis of SiO{sub 2}-coated Cu nanoparticles. • The antibacterial membrane is more resistant to oxidation and can prolong the antimicrobial activity.

  18. Preparation of nano-crystalline cellulose by chemical methods%化学法制备纳米微晶纤维素的研究进展

    Institute of Scientific and Technical Information of China (English)

    李媛媛; 戴红旗

    2012-01-01

    纳米微晶纤维素是一种制备原料来源广泛、成本低、在功能材料等领域有广泛应用前景的可再生新兴纤维素功能材料.然而纳米微晶纤维素的制备存在得率低、水耗大、对设备要求严格等缺点,限制了纳米微晶纤维素的大规模生产;因此寻找纳米微晶纤维素的绿色、高效制备方法显得尤为重要.笔者从原料和化学制备方法上综述了制备纳米微晶纤维素的研究进展,并对纳米微晶纤维素制备及纳米微晶纤维素基功能材料的进一步发展应用进行了展望.%Nano-crystalline cellulose is a renewable functional cellulose material with great application value in functional material and other fields. It can be obtained from a variety of sources at a low cost. However, there are many drawbacks such as low yield, huge water consumption as well as strict requirement on equipment in the preparation which limit the nanocrystalline cellulose from mass production. The isolation of nanocrystalline cellulose from cellulose fibers u-sing a green and effective method is a great challenge. In this paper, the development of nanocrystalline cellulose preparation was summarized from the aspects of raw materials to chemical preparation methods. In addition, further application and development in nanocrystalline cellulose preparation and nanocrystalline cellulose based functional materials were discussed.

  19. Dried blood spots on carboxymethyl cellulose sheets: Rapid sample preparation based on dissolution and precipitation

    DEFF Research Database (Denmark)

    Skoglund Ask, Kristine; Pedersen-Bjergaard, Stig; Gjelstad, Astrid

    2016-01-01

    This short communication describes the use of carboxymethyl cellulose sheets as sampling material for dried blood spots. Whole blood, spiked with quetiapine, a hydrophobic and basic small molecule drug substance, was spotted on the sheet and subsequently dried. The dried spot was then almost...

  20. Preparation of cellulose-based sponges for wound dressing and healing

    NARCIS (Netherlands)

    Kazlauske, J.; Dutschk, Victoria; Liesiene, J.; Dörfel, A.; Vignaesh Sankaran, M.

    2013-01-01

    For healing of chronic or burn wounds, polymeric sponges have been recently applied. Due to a high absorption capacity, noncitotoxicity and good swelling capabilities, for their production natural polymers are often used. In this study, macroporous regenerated cellulose was evaluated as a matrix for

  1. Preparation of cellulose-based sponges for wound dressing and healing

    NARCIS (Netherlands)

    Kazlauske, J.; Dutschk, V.; Liesiene, J.; Dörfel, A.; Vignaesh Sankaran, M.

    2013-01-01

    For healing of chronic or burn wounds, polymeric sponges have been recently applied. Due to a high absorption capacity, noncitotoxicity and good swelling capabilities, for their production natural polymers are often used. In this study, macroporous regenerated cellulose was evaluated as a matrix for

  2. Preparation and Application of Cationic Modified Cellulose Fibrils as a Papermaking Additive

    Directory of Open Access Journals (Sweden)

    Yanhong Gao

    2016-01-01

    Full Text Available This paper deals with cationic modified cellulose fibrils obtained by reacting the cellulose fibrils with 2,3-epoxypropyltrimethylammonium chloride (EPTMAC. The physical and chemical properties of unmodified cellulose fibrils (UMCF and cationic modified cellulose fibrils (CMCF were characterized by SEM, FTIR, degree of substitution, colloid titration, zeta potential, and thermogravimetric analysis. The experimental results showed that, after cationization, surface charge density and zeta potential reversed, thermal stability decreased, and new functional groups appeared, while the surface morphology did not show much difference from the UMCF. With the addition of three kinds of additives (UMCF, CMCF, and cationic starch (CS to BCTMP, the addition of UMCF and CMCF had little effect on zeta potential, while the addition of CS changed zeta potential obviously. With the increasing of additive amount, the bulk of paper sheets added CMCF did not change obviously, while the bulk of paper sheets added UMCF and CS decreased rapidly. With regard to physical strength, all the three kinds of additives could improve the tensile index and tear index; the tensile index of paper sheets added CS was higher than that of added UMCF and CMCF, while the tear index of paper sheets added CMCF was the highest among the three additives.

  3. Stability of thin films of microcrystalline silicon under light soaking

    Institute of Scientific and Technical Information of China (English)

    HAN Xiao-yan; Wang Yan; XUE Jun-ming; ZHAO Shu-wen; REN Hui-zhi; ZHAO Ying; LI Yang-xian; GENG Xin-hua

    2006-01-01

    Silicon thin films with different crystalline ratio(Xc) have been deposited by varying silane content(SC) of reactive gases in the RF-PECVD process.The effects of silane content on performance of the materials and the relationship between microstructure and opto-electronic properties were studied by means of Raman measurements,photoconductivity(σph),and dark conductivity(σd),followed by the measurements of light absorption coefficient(α),the product of quantum efficiency,mobility and lifetime (ημτ),before,during and after light soaking,respectively.The results indicate that the microcrystalline silicon near the transition region is suitable to prepare microcrystalline silicon of device grade,and that the amorphous region of the material is responsible to the light induced degradation.

  4. Preparation of cellulose nanocrystals from asparagus (Asparagus officinalis L.) and their applications to palm oil/water Pickering emulsion.

    Science.gov (United States)

    Wang, Wenhang; Du, Guanhua; Li, Cong; Zhang, Hongjie; Long, Yunduo; Ni, Yonghao

    2016-10-20

    Nano cellulosic materials as promising emulsion stabilizers have attracted great interest in food industry. In this paper, five different sized cellulose nanocrystals (CNC) samples were prepared from stem of Asparagus officinalis L. using the same sulfuric acid hydrolysis conditions but different times (1.5, 2, 2.5, 3.0, and 3.5h). The sizes of these CNC ranged from 178.2 to 261.8nm, with their crystallinity of 72.4-77.2%. The CNC aqueous dispersions showed a typical shear thinning behavior. In a palm oil/water (30/70, v/v) model solution, stable Pickering emulsions were formed with the addition of CNC, and their sizes are in the range of 1-10μm based on the optical and confocal laser scanning microscopy (CLSM) observation. The CNC sample prepared at 3h hydrolysis time, showed a relative efficient emulsion capacity for palm oil droplets, among these CNCs. Other parameters including the CNC, salt, and casein concentrations on the emulsion stability were studied.

  5. Cellulose nanocrystals prepared via formic acid hydrolysis followed by TEMPO-mediated oxidation.

    Science.gov (United States)

    Li, Bin; Xu, Wenyang; Kronlund, Dennis; Määttänen, Anni; Liu, Jun; Smått, Jan-Henrik; Peltonen, Jouko; Willför, Stefan; Mu, Xindong; Xu, Chunlin

    2015-11-20

    Cellulose nanocrystals (CNCs) as a renewable and biodegradable nanomaterial have wide application value. In this work, CNCs were extracted from bleached chemical pulp using two stages of isolation (i.e. formic acid (FA) hydrolysis and 2,2,6,6-tetramethyl-piperidine-1-oxyl (TEMPO) mediated oxidation) under mild conditions. In the first stage, FA was used to remove hemicellulose, swell cellulose fibers, and release CNCs. The FA could be readily recovered and reused. In the second stage, the CNCs isolated by FA were further modified by TEMPO-mediated oxidation to increase the surface charge of CNCs. It was found that the modified CNCs with more ordered crystal structure and higher surface charge had better redispersibility and higher viscosity in aqueous phase. Therefore, the modified CNCs could be more effective when used as rheology modifier in the fields of water based coating, paint, food etc. Copyright © 2015 Elsevier Ltd. All rights reserved.

  6. Preparation of reference material for uranium and plutonium measurements using cellulose compound as a stabilizer

    Energy Technology Data Exchange (ETDEWEB)

    Surugaya, Naoki; Sato, Soichi; Hina, Tetsuro; Hiyama, Toshiaki [Japan Nuclear Cycle Development Inst., Tokai Works, Tokai, Ibaraki (Japan)

    2003-03-01

    Isotope dilution mass spectrometry, considered the most reliable analytical technique for input accountancy measurements of uranium and plutonium in spent fuel reprocessing plants, requires a well-characterized uranium/plutonium spike. Solid spikes containing {sup 235}U and {sup 239}Pu have been successfully utilized in safeguards inspections and in accountability analysis. They contain relatively large amounts of uranium and plutonium isotopically different to the uranium and plutonium of the sample, and are usually in the dried nitrate form. However, it is difficult to maintain and guarantee the integrity of the spike over long periods as they are in the dried nitrate form that can flake off the glass ampoule surface. Organic coatings were investigated using cellulose acetate butyrate as a stabilizer. The cellulose acetate butyrate had good characteristics, maintaining a thin film for a long time. (author)

  7. Preparation of Cellulose Nanofibrils from Bamboo Pulp by Mechanical Defibrillation for Their Applications in Biodegradable Composites.

    Science.gov (United States)

    Guimarães, Mario; Botaro, Vagner Roberto; Novack, Kátia Monteiro; Neto, Wilson Pires Flauzino; Mendes, Lourival Marin; Tonoli, Gustavo H D

    2015-09-01

    There is a growing interest in cellulose nanofibrils from renewable sources for various industrial applications. However, there is a lack of information on cellulose arising from bamboo pulps. Nanofibrils from refined bamboo pulps, including bleached, unbleached, and unrefined/unbleached, were obtained by mechanical defibrillation for use in biodegradable composites. The influence of industrial processes, such as pulping and refining of unbleached pulps, as well as of alkali pretreatments and bleaching of refined pulps, on the chemical composition of the samples was analyzed. Morphological, structural, thermal, optical and viscometric properties were investigated as a function of the number of passages of refined/bleached suspensions through a defibrillator. For the unbleached suspensions, the effects of refining and bleaching on the properties of nanofibrils were evaluated, fixing the number of passages through the defibrillator. Microscopic studies demonstrated that nanoscale cellulose fibers were obtained from both pulps, with a higher yield for the refined/bleached and refined/unbleached pulp, at the expense of the unbleached/unrefined pulps. The study showed that, in addition to the effectiveness of the pre-treatments, there was an increase in the production efficiency of nanofibrils, as well as in the transparency of the bleached suspensions, while viscosity, thermal stability and crystallinity had reduced levels as the number of passages through the defibrillator increased, showing a gradual improvement in the transition from the micro- to the nano-scale. The present study contributed to the different methods that are available for the production of bamboo cellulose nanofibrils, which can be used in the production of biodegradable composites for various applications.

  8. Polylactide/acetylated nanocrystalline cellulose composites prepared by a continuous route: A phase interface-property relation study.

    Science.gov (United States)

    Xu, Chunjiang; Chen, Jianxiang; Wu, Defeng; Chen, Yang; Lv, Qiaolian; Wang, Mengqi

    2016-08-01

    A 'continuous route' was developed in this work for the preparation of nanocrystalline cellulose (NCC) filled polylactide (PLA) composites. It combines several separated steps, including extraction of NCC, surface acetylation of NCC, and final composite preparation, into a continuous process, without traditional freeze drying. The obtained PLA composites were then studied in terms of phase interface structure, rheological and mechanical properties. The results reveal that surface acetylation of NCC can improve its affinity to PLA evidently. The thickened interfacial layer makes the system filled with modified NCC show lower percolation threshold than the one filled with pristine NCC; and the former presents a typical strain-scaling stress overshoot behavior in the start-up shear flow because the network structure of modified NCC presents stronger characteristics of self-similarity. The phase interface adhesion also plays an important role in the mechanical behavior of PLA/NCC composites, which is further revealed by the nanomechanical analysis using atom force microscopy.

  9. Preparation and Characterization of Nanocrystalline Cellulose Catalyzed by Carbon-Based Phosphotungstic Acid%炭基磷钨酸催化制备纳米纤维素的研究

    Institute of Scientific and Technical Information of China (English)

    游惠娟; 曾常伟; 卢麒麟; 唐丽荣; 吴耿烽; 黄彪

    2014-01-01

    采用炭基磷钨酸在超声波辅助作用下水解微晶纤维素(MCC ),制备得到纳米纤维素晶体(NCC)。采用透射电子显微镜(TEM)、X射线衍射仪(XRD)、傅里叶变换红外光谱仪(FTIR)和热分析仪(TGA )等对所制备N C C的形貌、晶体结构、光谱性质和热稳定性进行分析。结果表明:制备的NCC呈棒状,直径和长度主要分布在12~79 nm和146~862 nm,样品仍属于纤维素Ⅰ型,结晶度为76.1%;FTIR分析可知,纳米纤维素晶体仍然具有纤维素的基本化学结构;TGA分析表明,纳米纤维素晶体热分解温度为300℃,初期热稳定性低于微晶纤维素。与常规酸水解方法相比,该方法在制备过程中可省去脱酸过程,具有对设备腐蚀性小、环保等优点。%Nanocrystalline cellulose (NCC)was prepared by ultrasonic-assisted hydrolysis of microcrystal-line cellulose (MCC ) with carbon-based phosphotungstic acid as the catalyst.The morphological,crystal structure,spectrum properties and thermal stability properties of NCC were respectively analyzed by transmis-sion electron microscopy (TEM),X-ray diffraction (XRD ),Fourier transformation infrared spectroscopy (FTIR),and thermographic analyzer (TGA).The results indicated that NCC was rod-like with diameter ran-ging around 10 -100 nm and length ranging between 200 -800 nm.The XRD pattern showed that the NCC still kept with the typeⅠcellulose structure,and its crystallinity was 76 .1%.The FTIR analysis showed that NCC was still with the basic chemical structure of cellulose.The results of TGA analysis demonstrated that the thermal decomposition temperature of NCC was 300℃,whose primary thermal stability of NCC was lower than that of MCC.Compared with the conventional acid hydrolysis,the new preparation approach of NCC could a-void the acid removing process,and it possessed the advantages of low corrosion to equipments,and less pollu-tion to the environment

  10. Controlled release metformin hydrochloride microspheres of ethyl cellulose prepared by different methods and study on the polymer affected parameters.

    Science.gov (United States)

    Choudhury, Pratim K; Kar, Mousumi

    2009-02-01

    The objectives of this investigation were to prepare microspheres of the anti-diabetic drug, metformin hydrochloride, using ethyl cellulose as the polymer and evaluate the encapsulation efficiency and release characteristics in vitro and in vivo; utilizing different microencapsulation techniques. Different proportions of polymer were used to obtain varying drug-polymer ratios. Physical properties, loading efficiency and dissolution rate were dependent on the method chosen for preparation and also on the drug-to-polymer ratio. The addition of surfactant during emulsification and petroleum ether in non-solvent addition process affected release of drug and also size distribution of microspheres. To investigate the type of mechanism that occurs, dissolution data were plotted according to different kinetic models. In vitro release studies show first order and Higuchi model release characteristics being exhibited. All the results were treated statistically to validate the findings. Significant differences in percentage yield, entrapment efficiency and sustaining capacity were seen with microspheres prepared by two different methods. In vivo studies in normal and hyperglycemic mice show faster glucose reduction with microspheres prepared by the evaporation method, whereas the release sustaining effect was more pronounced with microspheres prepared by the non-solvent addition method.

  11. Studies on preparation of aceclofenac pellets by centrifugal granulator

    Directory of Open Access Journals (Sweden)

    Zibin GAO

    Full Text Available To prepare aceclofenac pellets by centrifugal granulation. Using 90~100 g of starch pellets as the core pellets,100 g of aceclofenac mixed with 50 g of microcrystalline cellulose(MCC and 4 g talc, methyl cellulose (HPMC as binder,the aceclofenac pellets were prepared by centrifugal granulation .And evaluate the quality of the pellets. The aceclofenac pellets had high yield and less losses,the pellets had a partical size of 0.70~0.88 mm(18~24 mesh)and had uniform particle size .the moisture ,drug content and dissolution meet the requirement . Aceclofenac pellets were prepared by the process of centrifugal granulation .The preparation prescription and process parameters were optimized by single factor method .and the pellets meet the standard requirements.

  12. Rheological and mechanical study of regenerated cellulose/multi-walled carbon nanotube composites

    Science.gov (United States)

    Shao, Wei; Wang, Shuxia; Liu, Hui; Wu, Jimin; Huang, Min; Ma, Wenjing; Huang, Chaobo

    2016-09-01

    Regenerated cellulose (RC)-based composites reinforced with multi-walled carbon nanotubes (MWCNTs) were prepared by a facile casting method. The morphology and microstructure of the fabricated composites were characterized using transmission electron microscopy, Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy. Thermogravimetry and derivative thermogravimetric analysis were conducted to investigate the effect of MWCNTs on the thermal behaviors of the RC. The results showed that the introduction of MWCNTs enhanced the thermal stability of the RC. Moreover, the effect of the dispersion state of MWCNTs in microcrystalline cellulose/ZnCl2 solutions with varying MWCNT loadings was studied by rheological tests. The mechanical properties of composite films were remarkably improved compared to those of pure RC film. Specifically, the composite film containing 3 wt% of MWCNTs exhibits a 123% enhancement in tensile strength and a 163% enhancement in the Young’s modulus compared with the pure RC film.

  13. Surface Photochemistry: Benzophenone as a Probe for the Study of Modified Cellulose Fibres

    Directory of Open Access Journals (Sweden)

    L. F. Vieira Ferreira

    2007-01-01

    Full Text Available This work reports the use of benzophenone, a very well characterized probe, to study new hosts (i.e., modified celluloses grafted with alkyl chains bearing 12 carbon atoms by surface esterification. Laser-induced room temperature luminescence of air-equilibrated or argon-purged solid powdered samples of benzophenone adsorbed onto the two modified celluloses, which will be named C12-1500 and C12-1700, revealed the existence of a vibrationally structured phosphorescence emission of benzophenone in the case where ethanol was used for sample preparation, while a nonstructured emission of benzophenone exists when water was used instead of ethanol. The decay times of the benzophenone emission vary greatly with the solvent used for sample preparation and do not change with the alkylation degree in the range of 1500–1700 micromoles of alkyl chains per gram of cellulose. When water was used as a solvent for sample preparation, the shortest lifetime for the benzophenone emission was observed; this result is similar to the case of benzophenone adsorbed onto the “normal” microcrystalline cellulose surface, with this latter case previously reported by Vieira Ferreira et al. in 1995. This is due to the more efficient hydrogen abstraction reaction from the glycoside rings of cellulose when compared with hydrogen abstraction from the alkyl chains of the modified celluloses. Triplet-triplet transient absorption of benzophenone was obtained in both cases and is the predominant absorption immediately after laser pulse, while benzophenone ketyl radical formation occurs in a microsecond time scale both for normal and modified celluloses.

  14. Characterization of cellulose nanowhiskers; Caracterizacao do nanowhiskers de celulose

    Energy Technology Data Exchange (ETDEWEB)

    Nascimento, Nayra R.; Pinheiro, Ivanei F.; Morales, Ana R.; Ravagnani, Sergio P.; Mei, Lucia, E-mail: 25nareis@gmail.com [Universidade Estadual de Campinas (UNICAMP), SP (Brazil)

    2013-07-01

    Cellulose is the most abundant polymer earth. The cellulose nanowhiskers can be extracted from the cellulose. These have attracted attention for its use in nanostructured materials for various applications, such as nanocomposites, because they have peculiar characteristics, among them, high aspect ratio, biodegradability and excellent mechanical properties. This work aims to characterize cellulose nanowhiskers from microcrystalline cellulose. Therefore, these materials were characterized by X-ray diffraction (XRD) to assess the degree of crystallinity, infrared spectroscopy (FT-IR), transmission electron microscopy (TEM) to the morphology of nanowhiskers and thermal stability was evaluated by Thermogravimetric Analysis (TGA). (author)

  15. Tips and tricks to recognize microcrystalline arthritis

    National Research Council Canada - National Science Library

    Filippucci, Emilio; Di Geso, Luca; Grassi, Walter

    2012-01-01

    .... The knowledge of some tips and tricks in the identification of these findings can play a key role in exploiting the relevant potential of US in microcrystalline arthritis, avoiding errors and misinterpretations...

  16. Cellulose Isolation Methodology for NMR Analysis of Cellulose Ultrastructure

    Directory of Open Access Journals (Sweden)

    Art J. Ragauskas

    2011-11-01

    Full Text Available In order to obtain accurate information about the ultrastructure of cellulose from native biomass by 13C cross polarization magic angle spinning (CP/MAS NMR spectroscopy the cellulose component must be isolated due to overlapping resonances from both lignin and hemicellulose. Typically, cellulose isolation has been achieved via holocellulose pulping to remove lignin followed by an acid hydrolysis procedure to remove the hemicellulose components. Using 13C CP/MAS NMR and non-linear line-fitting of the cellulose C4 region, it was observed that the standard acid hydrolysis procedure caused an apparent increase in crystallinity of ~10% or less on the cellulose isolated from Populus holocellulose. We have examined the effect of the cellulose isolation method, particularly the acid treatment time for hemicellulose removal, on cellulose ultrastructural characteristics by studying these effects on cotton, microcrystalline cellulose (MCC and holocellulose pulped Populus. 13C CP/MAS NMR of MCC indicated that holocellulose pulping and acid hydrolysis has little effect on the crystalline ultrastructural components of cellulose. Although any chemical method to isolate cellulose from native biomass will invariably alter substrate characteristics, especially those related to regions accessible to solvents, we found those changes to be minimal and consistent in samples of typical crystallinity and lignin/hemicellulose content. Based on the rate of the hemicellulose removal, as determined by HPLC-carbohydrate analysis and magnitude of cellulose ultrastructural alteration, the most suitable cellulose isolation methodology utilizes a treatment of 2.5 M HCl at 100 °C for a standard residence time between 1.5 and 4 h. However, for the most accurate crystallinity results this residence time should be determined empirically for a particular sample.

  17. Preparation and characterization of a Lithium-ion battery separator from cellulose nanofibers

    Directory of Open Access Journals (Sweden)

    Hongfeng Zhang

    2015-10-01

    Full Text Available Optimizing the desired properties for stretch monolayer separators used in Lithium-ion batteries has been a challenge. In the present study a cellulose nanofiber/PET nonwoven composite separator is successfully fabricated, using a wet-laid nonwoven (papermaking process, which can attain optimal properties in wettability, mechanical strength, thermal resistance, and electrochemical performance simultaneously. The PET nonwoven material, which is fabricated from ultrafine PET fibers by a wet-laid process, is a mechanical support layer. The porous structure of the composite separator was created by cellulose nanofibers coating the PET in a papermaking process. Cellulose nanofibers (CNFs, which are an eco-friendly sustainable resource, have been drawing considerable attention due to their astounding properties, such as: incredible specific surface area, thermal and chemical stability, high mechanical strength and hydrophilicity. The results show that the CNF separator exhibits higher porosity (70% than a PP (polypropylene separator (40%. The CNF separator can also be wetted by electrolyte in a few seconds while a PP separator cannot be entirely wetted after 1 min. The CNF separator has an electrolyte uptake of 250%, while a PP separator has only 65%. Another notable finding is that the CNF separator has almost no shrinkage when exposed to 180 °C for 1 h, whereas a PP separator shrinks by more than 50%. Differential Scanning Calorimetry (DSC shows that the CNF separator has a higher melting point than a PP separator. These findings all indicate that the CNF 29 separator will be more favorable than stretch film for use in Lithium-ion batteries.

  18. Synthesis and Characterization of Storage Energy Materials Prepared from Nano-crystalline Cellulose/Polyethylene Glycol

    Institute of Scientific and Technical Information of China (English)

    Xiao Ping YUAN; En Yong DING

    2006-01-01

    This paper gives a brief report of the synthesis of a new kind of solid-solid phase change materials (SSPCMs), nano-crystalline cellulose/polyethylene glycol (NCC/PEG). These PCMs have very high ability for energy storage, and their enthalpies reach 103.8 J/g. They are composed of two parts, PEG as functional branches for energy storage, and NCC as skeleton. The flexible polymer PEG was grafted onto the surface of rigid powder of NCC by covalent bonds. The results of DSC, FT-IR were briefly introduced, and some comments were also given.

  19. Tips and tricks to recognize microcrystalline arthritis.

    Science.gov (United States)

    Filippucci, Emilio; Di Geso, Luca; Grassi, Walter

    2012-12-01

    US plays a useful role in diagnosing and monitoring therapy in microcrystalline arthritis, as it may detect both monosodium urate and calcium pyrophosphate crystal aggregates. The knowledge of some tips and tricks in the identification of these findings can play a key role in exploiting the relevant potential of US in microcrystalline arthritis, avoiding errors and misinterpretations. This review provides an in-depth description of simple technical and methodological issues to guide the rheumatologist in daily clinical practice.

  20. The preparation, characterization and evaluation of regenerated cellulose/collagen composite hydrogel films.

    Science.gov (United States)

    Cheng, Yongmei; Lu, Jinting; Liu, Shilin; Zhao, Peng; Lu, Guozhong; Chen, Jinghua

    2014-07-17

    Porous structured regenerated cellulose films were oxidized by periodate oxidation to obtain 2,3-dialdehyde cellulose (DARC) films, which were then reacted with collagen to obtain DARC/Col composite films. The subsequent FT-IR spectra indicated that collagen was immobilized on the DARC matrix via the Schiff base reaction between NH2 in collagen and CHO in DARC backbone. Scanning electron microscopy revealed that DARC/Col exhibited a refined 3D network structure and its porosity and pore size decreased with increasing of collagen concentration. The composite films demonstrated a good equilibrium-swelling ratio, air permeability and water retention properties. The composite films also showed excellent mechanical properties, which was vital for practical application. Finally, the cytotoxicity of the composite film was evaluated using NIH3T3 mice fibroblast cells, the results revealed that DARC/Col composite films have good biocompatibility for use as scaffold material in tissue engineering. Copyright © 2014 Elsevier Ltd. All rights reserved.

  1. Preparation and characterization of 2,3-dialdehyde bacterial cellulose for potential biodegradable tissue engineering scaffolds

    Energy Technology Data Exchange (ETDEWEB)

    Li Jian; Wan Yizao [School of Materials Science and Engineering, Tianjin University, Tianjin 300072 (China); Li Lianfeng [Technical Institute of Physics and Chemistry of CAS, Beijing 100080 (China); Liang Hui [School of Materials Science and Engineering, Tianjin University, Tianjin 300072 (China); Wang Jiehua, E-mail: jiehuaw_tju@yahoo.com [School of Agriculture and Bioengineering, Tianjin University, Tianjin 300072 (China)

    2009-06-01

    Bacterial cellulose (BC) is suitable for applications as scaffolds in tissue engineering due to its unique properties. However, BC is not enzymatically degradable in vivo and this has become an essential limiting factor in its potential applications. In this work, BC was modified by periodate oxidation to give rise to a biodegradable 2,3-dialdehyde bacterial cellulose (DABC). After characterization by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, thin-film X-ray diffractometry (XRD) and X-ray photoelectron spectroscopy (XPS), we demonstrated that the modified DABC nano-network was able to degrade into porous scaffold with micro-sized pores in water, phosphate buffered saline (PBS) and the simulated body fluid (SBF). The degradation process began from the oxidized amorphous part of the network and concurrently hydroxyapatite formed on the scaffold surface during the process in SBF. Our data also demonstrated that the tensile mechanical properties of the DABC nano-network were suitable for its use in tissue engineering scaffolds.

  2. Two-Sided Surface Oxidized Cellulose Membranes Modified with PEI: Preparation, Characterization and Application for Dyes Removal

    Directory of Open Access Journals (Sweden)

    Wei Wang

    2017-09-01

    Full Text Available Porous regenerated cellulose (RC membranes were prepared with cotton linter pulp as a raw material. These membranes were first oxidized on both sides by a modified (2,2,6,6-tetramethylpiperidin-1-yloxyl (TEMPO oxidation system using a controlled oxidation reaction technique. Then, the oxidized RC membranes were functionalized with polyethylenimine (PEI via the glutaraldehyde crosslinking method to obtain bifunctional (carboxyl and amino porous RC membranes, as revealed by Fourier transform infrared spectroscopy (FT-IR, elemental analysis and zeta potential measurement. The scanning electron microscopy (SEM and the tests of the mechanical properties and permeability characteristics of modified RC membranes demonstrated that the porous structure and certain mechanical properties could be retained. The adsorption performance of the modified membranes towards dyes was subsequently investigated. The modified membranes displayed good adsorption capacities, rapid adsorption equilibrium and removal efficiencies towards both anionic (xylenol orange (XO and cationic (methylene blue (MB dyes, making them suitable bioadsorbents for wastewater treatment.

  3. Preparation of urea-formaldehyde paraffin microcapsules modified by carboxymethyl cellulose as a potential phase change material

    Institute of Scientific and Technical Information of China (English)

    Zhan-hua Huang; Xin Yu; Wei Li; Shou-xin Liu

    2015-01-01

    We prepared spherical microcapsules modified by carboxymethyl cellulose (CMC) with urea-formalde-hyde (UF) resin as a shell material with a two-step process by in situ polymerization, and characterized the micro-cosmic features, chemical structure, and thermal perfor-mance of the microcapsules by SEM, FTIR, DSC, and TGA. We studied the effects of different experimental parameters of curing pH, the amounts of the emulsifier and emulsion speed. The CMC-UF microcapsules had good heat resistance and stability. The enthalpy of CMC-UF microcapsules reached 50.33 J g-1. Therefore, CMC-UF resin can be used as a potential wall material of phase change materials.

  4. Preparation and antibacterial activity of silver nanoparticles impregnated in bacterial cellulose

    Directory of Open Access Journals (Sweden)

    Luiz C. S. Maria

    2010-01-01

    Full Text Available A simple method was developed to load a large amount of silver nanoparticles into bacterial cellulose (BC produced by Gluconacetobacter xylinus in a controlled manner. Due to the high electron-rich oxygen density in the BC macromolecules and the large surface area of the BC nanoporous structure as an effective nanoreactor, the in situ direct metallization technique was successfully used to synthesize Ag nanoparticles with an average diameter of 30 nm and a loading content of at least 5 wt. (%, approximately. This novel procedure provides an easy and economical way to manufacture Ag nanoparticles supported on a porous membrane for various biomedical applications. These composite fibers showed nearly 100% antibacterial activity (elimination of microorganisms against Escherichia coli because of the presence of the silver nanoparticles.

  5. Carboxymethyl Cellulose Acetate Butyrate: A Review of the Preparations, Properties, and Applications

    Directory of Open Access Journals (Sweden)

    Mohamed El-Sakhawy

    2014-01-01

    Full Text Available Carboxymethyl cellulose acetate butyrate (CMCAB has gained increasing importance in several fields, particularly in coating technologies and pharmaceutical research. CMCAB is synthesized by esterification of CMC sodium salt with acetic and butyric anhydrides. CMCAB mixed esters are relatively high molecular weight (MW thermoplastic polymers with high glass transition temperatures (Tg. CMCAB ester is dispersible in water and soluble in a wide range of organic solvents, allowing varied opportunity to the solvent choice. It makes application of coatings more consistent and defect-free. Its ability to slow down the release rate of highly water-soluble compounds and to increase the dissolution of poorly soluble compounds makes CMCAB a unique and potentially valuable tool in pharmaceutical and amorphous solid dispersions (ASD formulations.

  6. Properties of plasticized composite films prepared from nanofibrillated cellulose and birch wood xylan

    DEFF Research Database (Denmark)

    Hansen, Natanya Majbritt Louie; Blomfeldt, Thomas O. J.; Hedenqvist, Mikael S.

    2012-01-01

    Xylans, an important sub-class of hemicelluloses, represent a largely untapped resource for new renewable materials derived from biomass. As with other carbohydrates, nanocellulose reinforcement of xylans is interesting as a route to new bio-materials. With this in mind, birch wood xylan was comb......Xylans, an important sub-class of hemicelluloses, represent a largely untapped resource for new renewable materials derived from biomass. As with other carbohydrates, nanocellulose reinforcement of xylans is interesting as a route to new bio-materials. With this in mind, birch wood xylan...... was combined with nanofibrillated cellulose (NFC) and films were cast with and without glycerol, sorbitol or methoxypolyethylene glycol (MPEG) as plasticizers. Microscopy revealed some NFC agglomeration in the composite films as well as a layered nanocellulose structure. Equilibrium moisture content...

  7. Prevalence and trends of cellulosics in pharmaceutical dosage forms.

    Science.gov (United States)

    Mastropietro, David J; Omidian, Hossein

    2013-02-01

    Many studies have shown that cellulose derivatives (cellulosics) can provide various benefits when used in virtually all types of dosage forms. Nevertheless, the popularity of their use in approved drug products is rather unknown. This research reports the current prevalence and trends of use for 15 common cellulosics in prescription drug products. The cellulosics were powdered and microcrystalline cellulose (MCC), ethyl cellulose, hydroxypropyl cellulose (HPC), hydroxyethyl cellulose (HEC), hypromellose (HPMC), HPMC phthalate, HPMC acetate succinate, cellulose acetate (CA), CA phthalate, sodium (Na) and calcium (Ca) carboxymethylcellulose (CMC), croscarmellose sodium (XCMCNa), methyl cellulose, and low substituted HPC. The number of brand drug products utilizing each cellulosics was determined using the online drug index Rxlist. A total of 607 brand products were identified having one or more of the cellulosics as an active or inactive ingredient. An array of various dosage forms was identified and revealed HPMC and MCC to be the most utilized cellulosics in all products followed by XCMCNa and HPC. Many products contained two or more cellulosics in the formulation (42% containing two, 23% containing three, and 4% containing 4-5). The largest combination occurrence was HPMC with MCC. The use of certain cellulosics within different dosage form types was found to contain specific trends. All injectables utilized only CMCNa, and the same with all ophthalmic solutions utilizing HPMC, and otic suspensions utilizing HEC. Popularity and trends regarding cellulosics use may occur based on many factors including functionality, safety, availability, stability, and ease of manufacturing.

  8. A Facile Low-Temperature Hydrothermal Method to Prepare Anatase Titania/Cellulose Aerogels with Strong Photocatalytic Activities for Rhodamine B and Methyl Orange Degradations

    Directory of Open Access Journals (Sweden)

    Caichao Wan

    2015-01-01

    Full Text Available A facile low-temperature hydrothermal method for in situ preparation of anatase titania (TiO2 homogeneously dispersed in cellulose aerogels substrates was described. The formed anatase TiO2 aggregations composed of a mass of evenly dispersed TiO2 nanoparticles with sizes of 2−5 nm were embedded in the interconnected three-dimensional (3D architecture of the cellulose aerogels matrixes without large-scale reunion phenomenon; meanwhile, the obtained anatase titania/cellulose (ATC aerogels also had a high loading amount of TiO2 (ca. 35.7%. Furthermore, compared with commercially available Degussa P25, ATC aerogels displayed comparable photocatalytic activities for Rhodamine B and methyl orange degradations under UV radiation, which might be useful in the fields of catalysts, wastewater treatment, and organic pollutant degradation. Meanwhile, the photocatalytic reaction behaviors of ATC aerogels under UV irradiation were also illuminated.

  9. Research Progress of Biomimetic Material Prepared by Bacterial Cellulose%细菌纤维素制备生物医用材料的研究进展

    Institute of Scientific and Technical Information of China (English)

    蔡锐波; 陈海宏; 陈向标

    2012-01-01

    Bacterial cellulose(BC) is a potential versatile biomaterial. Research progress of medical dressing, vascular prosthesis and artificial skeleton prepared by bacterial cellulose were introduced at home and abroad. In addition, the hot spots and the main development direction of bacterial cellulose composite biomimetic materials were discussed.%细菌纤维素是一种很有潜力的新型生物纤维材料.重点介绍了国内外关于细菌纤维素在制备医用敷料、人造血管及人造骨骼等医用材料方面的研究进展,并指出今后的研究热点及主要发展方向.

  10. Preparation of Bacterial Cellulose/Inorganic Gel of Bentonite Composite by In Situ Modification.

    Science.gov (United States)

    Wang, Bo; Qi, Gao-Xiang; Huang, Chao; Yang, Xiao-Yan; Zhang, Hai-Rong; Luo, Jun; Chen, Xue-Fang; Xiong, Lian; Chen, Xin-De

    2016-03-01

    To evaluate the possibility of Bacterial cellulose/Inorganic Gel of Bentonite (BC/IGB) composite production using in situ method, the BC/IGB composite was successfully produced by in situ modification of BC in both HS medium and corncob hydrolysate. The results showed that the BC/IGB composite obtained in HS medium (one classical medium for BC production) had a higher water holding capacity, but the water retention capacity of the BC/IGB composite obtained in corncob hydrolysate was better. The performance of BC/IGB composite depended on the environment of in situ modification. Using different media showed significant influence on the sugar utilization and BC yield. In addition, BC/IGB composite produced by in situ method was compared with that produced by ex situ method, and the results shows that water holding capacity of BC/IGB composite obtained through in situ method was better. XRD results showed the crystallinity of BC/IGB composite related little to its performance as water absorbent. Overall, in situ modification is appropriate for further production of BC composite and other clay materials.

  11. Charge density modification of carboxylated cellulose nanocrystals for stable silver nanoparticles suspension preparation

    Energy Technology Data Exchange (ETDEWEB)

    Hoeng, Fanny; Denneulin, Aurore [Université Grenoble Alpes, LGP2 (France); Neuman, Charles [Poly-Ink (France); Bras, Julien, E-mail: julien.bras@grenoble-inp.fr [Université Grenoble Alpes, LGP2 (France)

    2015-06-15

    Synthesis of silver nanoparticles using cellulose nanocrystals (CNC) has been found to be a great method for producing metallic particles in a sustainable way. In this work, we propose to evaluate the influence of the charge density of 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO)-oxidized CNC on the morphology and the stability of synthetized silver nanoparticles. Silver nanoparticles were obtained by sol–gel reaction using borohydride reduction, and charge density of TEMPO-oxidized CNC was tuned by an amine grafting. The grafting was performed at room temperature and neutral pH. Crystallinity and morphology were kept intact during the peptidic reaction on CNC allowing knowing the exact impact of the charge density. Charge density has been found to have a strong impact on shape, organization, and suspension stability of resulting silver particles. Results show an easy way to tune the charge density of CNC and propose a sustainable way to control the morphology and stability of silver nanoparticles in aqueous suspension.

  12. Preparation of micro-fibrillated cellulose from sorghum fibre through alkalization and acetylation treatments

    Science.gov (United States)

    Ismojo; Simanulang, P. H.; Zulfia, A.; Chalid, M.

    2017-07-01

    Recently, the pollution due to non-degradable materials including plastics, has led to needs on the development of environmental-friendly material. Owing to its biodegradability nature, sorghum fibres are interesting to be modified with petro-polymer as a composite. These materials are also expected to reduce the impact of environmental pollution. Surface modification of sorghum through chemical treatment was aimed to enhanced crystalline part of micro-fibrillated cellulose, thus increased compatibility to petro-polymer, as mean to improve composite properties. The experiments were conducted by alkalization process (10% NaOH) followed by acetylation with acetic acid glacial and acetic anhydride (CH3CO2)2 with additions of 1 and 2 drops of 25% H2SO4. Fourier transform infra-red (FTIR) spectroscopy, field-emission scanning electron microscope (FE-SEM) and x-ray diffraction (XRD) were used to characterize the treated and untreated fibres. The results of investigation showed that the chemical treatments have effectively produced MFC with the smallest fibre size around 5.5 - 6.5 microns and reduced lignin and hemicellulose where the highest crystalline part up to 80.64% was obtained through acetate acid treatment of 17.4 M, followed acetic anhydride with 1 drop of H2SO4 addition. Based on the current results, it is promising that the synthesized composites can be improved for their compatibilities.

  13. Preparation of Photocrosslinked Fish Elastin Polypeptide/Microfibrillated Cellulose Composite Gels with Elastic Properties for Biomaterial Applications

    Science.gov (United States)

    Yano, Shinya; Mori, Megumi; Teramoto, Naozumi; Iisaka, Makoto; Suzuki, Natsumi; Noto, Masanari; Kaimoto, Yasuko; Kakimoto, Masashi; Yamada, Michio; Shiratsuchi, Eri; Shimasaki, Toshiaki; Shibata, Mitsuhiro

    2015-01-01

    Photocrosslinked hydrogels reinforced by microfibrillated cellulose (MFC) were prepared from a methacrylate-functionalized fish elastin polypeptide and MFC dispersed in dimethylsulfoxide (DMSO). First, a water-soluble elastin peptide with a molecular weight of ca. 500 g/mol from the fish bulbus arteriosus was polymerized by N,N′-dicyclohexylcarbodiimide (DCC), a condensation reagent, and then modified with 2-isocyanatoethyl methacrylate (MOI) to yield a photocrosslinkable fish elastin polypeptide. The product was dissolved in DMSO and irradiated with UV light in the presence of a radical photoinitiator. We obtained hydrogels successfully by substitution of DMSO with water. The composite gel with MFC was prepared by UV irradiation of the photocrosslinkable elastin polypeptide mixed with dispersed MFC in DMSO, followed by substitution of DMSO with water. The tensile test of the composite gels revealed that the addition of MFC improved the tensile properties, and the shape of the stress–strain curve of the composite gel became more similar to the typical shape of an elastic material with an increase of MFC content. The rheology measurement showed that the elastic modulus of the composite gel increased with an increase of MFC content. The cell proliferation test on the composite gel showed no toxicity. PMID:25584682

  14. Preparation of Photocrosslinked Fish Elastin Polypeptide/Microfibrillated Cellulose Composite Gels with Elastic Properties for Biomaterial Applications

    Directory of Open Access Journals (Sweden)

    Shinya Yano

    2015-01-01

    Full Text Available Photocrosslinked hydrogels reinforced by microfibrillated cellulose (MFC were prepared from a methacrylate-functionalized fish elastin polypeptide and MFC dispersed in dimethylsulfoxide (DMSO. First, a water-soluble elastin peptide with a molecular weight of ca. 500 g/mol from the fish bulbus arteriosus was polymerized by N,N′-dicyclohexylcarbodiimide (DCC, a condensation reagent, and then modified with 2-isocyanatoethyl methacrylate (MOI to yield a photocrosslinkable fish elastin polypeptide. The product was dissolved in DMSO and irradiated with UV light in the presence of a radical photoinitiator. We obtained hydrogels successfully by substitution of DMSO with water. The composite gel with MFC was prepared by UV irradiation of the photocrosslinkable elastin polypeptide mixed with dispersed MFC in DMSO, followed by substitution of DMSO with water. The tensile test of the composite gels revealed that the addition of MFC improved the tensile properties, and the shape of the stress–strain curve of the composite gel became more similar to the typical shape of an elastic material with an increase of MFC content. The rheology measurement showed that the elastic modulus of the composite gel increased with an increase of MFC content. The cell proliferation test on the composite gel showed no toxicity.

  15. Preparation of polyvinylidene fluoride/cellulose acetate blend membrane with polyethylene glycol additive for apple juice clarification

    Science.gov (United States)

    Fitri, Shatila Jihadiyah; Widiastuti, Nurul

    2017-03-01

    Polyvinylidene Fluoride (PVDF)/Cellulose Acetate (CA) blend membrane with polyethylene (PEG) addition of casting solution were synthesised to determine its morphology. This purpose of this research is to investigate the effect of PEG addition to membrane performance and its application to the clarification of apple juice. The membranes were prepared from polymer blends of CA and PVDF, dimethyl acetamide (DMAc) as solvent, and PEG as additive. Phase inversion was used to prepare membranes by mixing the polymer blends, solvent and additive to be reacted at temperature 60 °C for 24 hours. The variation of PEG weight percentage were 0, 1 wt%, 3 wt%, and 5 wt%. The addition of PEG increased porosity and fluxes, but decreased membrane rejection. Scanning Electron Microscope (SEM), Atomic Force Microscope (AFM), and Fourier Transform Infrared (FTIR) were applied to evaluate the morphology of membranes, which investigated increasing of pore size, pore distribution, and surface roughness. Apple juice clarification by membrane with 1% PEG was obtained 95,1% clearer than the pure sample.

  16. Efficient Pb(II) removal using sodium alginate-carboxymethyl cellulose gel beads: Preparation, characterization, and adsorption mechanism.

    Science.gov (United States)

    Ren, Huixue; Gao, Zhimin; Wu, Daoji; Jiang, Jiahui; Sun, Youmin; Luo, Congwei

    2016-02-10

    Alginate-carboxymethyl cellulose (CMC) gel beads were prepared in this study using sodium alginate (SA) and sodium CMC through blending and cross-linking. The specific surface area and aperture of the prepared SA-CMC gel beads were tested. The SA-CMC structure was characterized and analyzed via infrared spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. Static adsorption experiment demonstrated that Pb(II) adsorption of SA-CMC exceeded 99% under the optimized conditions. In addition, experiments conducted under the same experimental conditions showed that the lead ion removal efficiency of SA-CMC was significantly higher than that of conventional adsorbents. The Pb(II) adsorption process of SA-CMC followed the Langmuir adsorption isotherm, and the dynamic adsorption model could be described through a pseudo-second-order rate equation. Pb(II) removal mechanisms of SA-CMC, including physical, chemical, and electrostatic adsorptions, were discussed based on microstructure analysis and adsorption kinetics. Chemical adsorption was the main adsorption method among these mechanisms. Copyright © 2015 Elsevier Ltd. All rights reserved.

  17. Preparation of photocrosslinked fish elastin polypeptide/microfibrillated cellulose composite gels with elastic properties for biomaterial applications.

    Science.gov (United States)

    Yano, Shinya; Mori, Megumi; Teramoto, Naozumi; Iisaka, Makoto; Suzuki, Natsumi; Noto, Masanari; Kaimoto, Yasuko; Kakimoto, Masashi; Yamada, Michio; Shiratsuchi, Eri; Shimasaki, Toshiaki; Shibata, Mitsuhiro

    2015-01-09

    Photocrosslinked hydrogels reinforced by microfibrillated cellulose (MFC) were prepared from a methacrylate-functionalized fish elastin polypeptide and MFC dispersed in dimethylsulfoxide (DMSO). First, a water-soluble elastin peptide with a molecular weight of ca. 500 g/mol from the fish bulbus arteriosus was polymerized by N,N'-dicyclohexylcarbodiimide (DCC), a condensation reagent, and then modified with 2-isocyanatoethyl methacrylate (MOI) to yield a photocrosslinkable fish elastin polypeptide. The product was dissolved in DMSO and irradiated with UV light in the presence of a radical photoinitiator. We obtained hydrogels successfully by substitution of DMSO with water. The composite gel with MFC was prepared by UV irradiation of the photocrosslinkable elastin polypeptide mixed with dispersed MFC in DMSO, followed by substitution of DMSO with water. The tensile test of the composite gels revealed that the addition of MFC improved the tensile properties, and the shape of the stress-strain curve of the composite gel became more similar to the typical shape of an elastic material with an increase of MFC content. The rheology measurement showed that the elastic modulus of the composite gel increased with an increase of MFC content. The cell proliferation test on the composite gel showed no toxicity.

  18. Development of Doped Microcrystalline Silicon Oxide and its Application to Thin‑Film Silicon Solar Cells

    NARCIS (Netherlands)

    Lambertz, A.

    2015-01-01

    The aim of the present study is the development of doped microcrystalline silicon oxide (µc‑SiOx:H) alloys and its application in thin‑film silicon solar cells. The doped µc‑SiOx:H material was prepared from carbon dioxide (CO2), silane (SiH4), hydrogen (H2) gas mixtures using plasma enhanced

  19. Development of Doped Microcrystalline Silicon Oxide and its Application to Thin‑Film Silicon Solar Cells

    NARCIS (Netherlands)

    Lambertz, A.

    2015-01-01

    The aim of the present study is the development of doped microcrystalline silicon oxide (µc‑SiOx:H) alloys and its application in thin‑film silicon solar cells. The doped µc‑SiOx:H material was prepared from carbon dioxide (CO2), silane (SiH4), hydrogen (H2) gas mixtures using plasma enhanced chemic

  20. 以离子液体为溶剂制备纤维素微球%Cellulose microspheres preparation using ionic liquid as the solvent

    Institute of Scientific and Technical Information of China (English)

    侯祥; 魏立纲; 马英冲; 李坤兰; 王少君; 余加祐

    2011-01-01

    Cellulose microspheres were prepared using the cellulose-ionic liquid (ID solution was prepared by directly dissolving by reversed -phase suspension technique. Effects of the used cellulose type, cellulose content in the solution, disperse phase, agitation speed, temperature on particle size distribution were discussed. In the case of 2% cotton cellulose/IL solution, heat transfer oil as disperse phase, 50:1 of volume ratio of oil and solution, PEG 600 as disperse agent, 500 r/min of the agitation speed and 80 °C, 55% cellulose microspheres with particle size 0.45 to 0.20 mm can be obtained.%将天然纤维素溶于离子液体中,制成纤维素/离子液体溶液,并以纤维素/离子液体溶液为原料采用悬浮聚合法制备了纤维素微球.讨论了纤维素种类和质量分数、纤维素/离子液体溶液与导热油体积比、搅拌速度和制备温度对纤维素微球粒径分布的影响.结果表明,质量分数为2%的棉纤维素/离子液体溶液,以导热油为分散相,V(纤维素/离子液体溶液):V(导热油)=1:50,聚乙二醇(相对分子质量600)作为分散剂,搅拌速度为500 r/min,制备温度为80℃,可制得粒径分布在0.45~0.20 mm占55%以上的纤维素微球.

  1. Matrix mini-tablets based on starch/microcrystalline wax mixtures.

    Science.gov (United States)

    De Brabander, C; Vervaet, C; Fiermans, L; Remon, J P

    2000-04-20

    Matrix mini-tablets based on a combination of microcrystalline waxes and starch derivatives were prepared using ibuprofen as a model drug. The production of mini-tablets was preferred over the production of pellets, as up-scaling of the pelletisation process seemed problematic. Prior to tabletting, melt granulation in a hot stage screw extruder and milling were required. The in vitro drug release was varied using microcrystalline waxes with a different melting range, the slowest drug release being obtained with a formulation containing a microcrystalline wax with a melting range between 68 and 72 degrees C. Generally speaking increasing the wax concentration resulted in a slower drug release. In vitro drug release profiles were also modified using different starches and mixtures of starches. Increasing the ibuprofen concentration to 70% resulted in a faster drug release rate.

  2. Nanocrystalline cellulose extracted from pine wood and corncob.

    Science.gov (United States)

    Ditzel, Fernanda I; Prestes, Eduardo; Carvalho, Benjamim M; Demiate, Ivo M; Pinheiro, Luís A

    2017-02-10

    The extraction of nanocrystalline cellulose from agro-residues is an interesting alternative to recover these materials. In the present study, nanocrystalline cellulose was extracted from pine wood and corncob. In addition, microcrystalline cellulose was used as a reference to compare results. Initially, the lignocellulosic residues were submitted to delignification pre-treatments. At the end of the process, the bleached fibre was submitted to acid hydrolysis. Additionally, microparticles were obtained from the spray-drying of the nanocrystalline cellulose suspensions. The nanocrystalline cellulose yield for the pine wood was 9.0-% of the value attained for the microcrystalline cellulose. For the corncob, the value was 23.5-%. Therefore, complementary studies are necessary to improve the yield. The spray-dried microparticles showed a crystallinity index of 67.8-% for the pine wood, 70.9-% for the corncob and 79.3-% for the microcrystalline cellulose. These microparticles have great potential for use in the production of polymer composites processed by extrusion.

  3. Spatially Resolved Characterization of Cellulose Nanocrystal-Polypropylene Composite by Confocal Raman Microscopy

    Science.gov (United States)

    Umesh P. Agarwal; Ronald Sabo; Richard S. Reiner; Craig M. Clemons; Alan W. Rudie

    2012-01-01

    Raman spectroscopy was used to analyze cellulose nanocrystal (CNC)–polypropylene (PP) composites and to investigate the spatial distribution of CNCs in extruded composite filaments. Three composites were made from two forms of nanocellulose (CNCs from wood pulp and the nanoscale fraction of microcrystalline cellulose) and two of the three composites investigated used...

  4. Negative results of growing titania nanotubes on cellulose nanocrystals - Effect of hydrothermal reaction

    Science.gov (United States)

    Chamakh, Mariem Mohamed; Ponnamma, Deepalekshmi; Al-Maadeed, Mariam Al Ali

    Titania nanotubes (TiO2 nanotubes or TNT) are grown hydrothermally on cellulose nanocrystals (CNC) synthesized from microcrystalline cellulose. It is observed that the CNC are lost during synthesis due to its low thermal stability. This negative result of metal growth on CNC and its influence on thermal degradation are reported here.

  5. Preparation and Properties of Cellulose Laurate (CL/Starch Nanocrystals Acetate (SNA Bio-nanocomposites

    Directory of Open Access Journals (Sweden)

    Feng-Yuan Huang

    2015-07-01

    Full Text Available In the present paper, a series of totally novel bio-nanocomposite films from cellulose laurate (CL and starch nanocrystals acetate (SNA were fabricated, and the properties of nanocomposite films were investigated in detail. SNA was obtained by modifying starch nanocrystals (SNs produced by sulfuric acid hydrolysis of corn starch with acetic anhydride. The favorable dispersity of SNA in chloroform made it ready to convert into nanocomposite films with CL via casting/evaporation method. The transmittance, thermal behavior, mechanical properties, barrier properties and hydrophobicity of CL/SNA nanocomposite films were investigated with UV-vis spectrophotometer, simultaneous thermal analyzer (STA, universal tensile tester/dynamic thermomechanical analysis (DMA, water vapor permeation meter/oxygen permeability tester, and contact angle tester, respectively. The transmittance of nanocomposite films decreased with the increase of SNA content. Thermogravimetric analysis (TGA results showed that the introduction of SNA into CL matrix did not severely decrease the thermal behavior of CL/SNA nanocomposites. Moreover, non-linear and linear mechanical analysis reflected the enhancement of SNA. At lower contents of SNA (<5.0 wt%, the values of Young’s modulus, tensile strength and the elongation at break of nanocomposite films were comparable with those of neat CL. However, with the increase of SNA, the Young’s modulus and tensile strength were improved significantly and were accompanied by the decreased elongation at break. The water vapor permeability (WVP and oxygen permeability (PO2 of CL/SNA nanocomposite films were significantly improved by the addition of SNA.

  6. Synthesis of Cellulose-2,3-bis(3,5-dimethylphenylcarbamate) in an Ionic Liquid and Its Chiral Separation Efficiency as Stationary Phase

    Science.gov (United States)

    Liu, Runqiang; Zhang, Yijun; Bai, Lianyang; Huang, Mingxian; Chen, Jun; Zhang, Yuping

    2014-01-01

    A chiral selector of cellulose-2,3-bis(3,5-dimethylphenylcarbamate) (CBDMPC) was synthesized by reacting 3,5-dimethylphenyl isocyanate with microcrystalline cellulose dissolved in an ionic liquid of 1-allyl-3-methyl-imidazolium chloride (AMIMCl). The obtained chiral selector was effectively characterized by infrared spectroscopy, elemental analysis and 1H NMR. The selector was reacted with 3-aminopropylsilanized silica gel and the CBDMPC bonded chiral stationary phase (CSP) was obtained. Chromatographic evaluation of the prepared CSPs was conducted by high performance liquid chromatographic (HPLC) and baseline separation of three typical fungicides including hexaconazole, metalaxyl and myclobutanil was achieved using n-hexane/isopropanol as the mobile phase with a flow rate 1.0 mL/min. Experimental results also showed that AMIMCl could be recycled easily and reused in the preparation of CSPs as an effective reaction media. PMID:24733066

  7. Synthesis of Cellulose-2,3-bis(3,5-dimethylphenylcarbamate in an Ionic Liquid and Its Chiral Separation Efficiency as Stationary Phase

    Directory of Open Access Journals (Sweden)

    Runqiang Liu

    2014-04-01

    Full Text Available A chiral selector of cellulose-2,3-bis(3,5-dimethylphenylcarbamate (CBDMPC was synthesized by reacting 3,5-dimethylphenyl isocyanate with microcrystalline cellulose dissolved in an ionic liquid of 1-allyl-3-methyl-imidazolium chloride (AMIMCl. The obtained chiral selector was effectively characterized by infrared spectroscopy, elemental analysis and 1H NMR. The selector was reacted with 3-aminopropylsilanized silica gel and the CBDMPC bonded chiral stationary phase (CSP was obtained. Chromatographic evaluation of the prepared CSPs was conducted by high performance liquid chromatographic (HPLC and baseline separation of three typical fungicides including hexaconazole, metalaxyl and myclobutanil was achieved using n-hexane/isopropanol as the mobile phase with a flow rate 1.0 mL/min. Experimental results also showed that AMIMCl could be recycled easily and reused in the preparation of CSPs as an effective reaction media.

  8. Cellulose with a High Fractal Dimension Is Easily Hydrolysable under Acid Catalysis

    Directory of Open Access Journals (Sweden)

    Mariana Díaz

    2017-05-01

    Full Text Available The adsorption of three diverse amino acids couples onto the surface of microcrystalline cellulose was studied. Characterisation of modified celluloses included changes in the polarity and in roughness. The amino acids partially break down the hydrogen bonding network of the cellulose structure, leading to more reactive cellulose residues that were easily hydrolysed to glucose in the presence of hydrochloric acid or tungstophosphoric acid catalysts. The conversion of cellulose and selectivity for glucose was highly dependent on the self-assembled amino acids adsorbed onto the cellulose and the catalyst.

  9. Microcrystalline hexagonal tungsten bronze. 2. Dehydration dynamics.

    Science.gov (United States)

    Luca, Vittorio; Griffith, Christopher S; Hanna, John V

    2009-07-06

    Low-temperature (25-600 degrees C) thermal transformations have been studied for hydrothermally prepared, microcrystalline hexagonal tungsten bronze (HTB) phases A(x)WO(3+x/2).zH(2)O as a function of temperature, where A is an exchangeable cation (in this case Na(+) or Cs(+)) located in hexagonal structural tunnels. Thermal treatment of the as-prepared sodium- and cesium-exchanged phases in air were monitored using a conventional laboratory-based X-ray diffractometer, while thermal transformations in vacuum were studied using synchrotron X-ray and neutron diffraction. Concurrent thermogravimetric, diffuse reflectance infrared (DRIFT), and (23)Na and (133)Cs magic angle spinning (MAS) NMR spectroscopic studies have also been undertaken. For the cesium variant, cell volume contraction occurred from room temperature to about 350 degrees C, the regime in which water was "squeezed" out of tunnel sites. This was followed by a lattice expansion in the 350-600 degrees C temperature range. Over the entire temperature range, a net thermal contraction was observed, and this was the result of an anisotropic change in the cell dimensions which included a shortening of the A-O2 bond length. These changes explain why Cs(+) ions are locked into tunnel positions at temperatures as low as 400 degrees C, subsequently inducing a significant reduction in Cs(+) extractability under low pH (nitric acid) conditions. The changing Cs(+) speciation as detected by (133)Cs MAS NMR showed a condensation from multiple Cs sites, presumably associated with differing modes of Cs(+) hydration in the tunnels, to a single Cs(+) environment upon thermal transformation and water removal. While similar lattice contraction was observed for the as-prepared sodium variant, the smaller radius of Na(+) caused it to be relatively easily removed with acid in comparison to the Cs(+) variant. From (23)Na MAS NMR studies of the parent material, complex Na(+) speciation was observed with dehydrated and various

  10. 纤维素-丝素复合膜的制备与表征%Preparation and characterization of cellulose/silk composite membrane

    Institute of Scientific and Technical Information of China (English)

    李娟; 何建新; 余燕平

    2011-01-01

    The cellulose-silk fibroin composite film is prepared by mixing cellulose solution dissolved primary wood pulp in solution containing of NaOH/urea/thiourea/water and silk fibroin solution. The composite film is characterized by scanning electron microscope (SEM) , Fourier transform infrared spectrometer (FT-IR) , X-ray diffraction (XRD). SEM shows the surface of the composite is uniform and rough. The as-prepared composite film may be a potential biomedical material. The results of IR and XRD show that composite film is composed of cellulose and silk fibroin molecules and exists an interaction including hydrogen bond between the molecular of cellulose and silk fibroin.%通过NaOH/尿素/硫脲/水新型溶剂溶解原生木浆纤维素得到纤维素溶液,并与丝素溶液混合制备纤维素-丝素复合膜.利用扫描电镜、红外光谱、X-射线衍射对复合材料的结构进行表征.SEM结果表明复合材料表面粗糙,比表面积较大,可以作为潜在的生物医用材料.IR和X-衍射结果表明再生纤维素与丝素分子之间存在着强烈的氢键作用,且二者相容性较好.

  11. Preparation, characterization, and activity of a peptide-cellulosic aerogel protease sensor from cotton

    Science.gov (United States)

    Nanocellulosic aerogels (NA) provide a lightweight biocompatible material with structural properties of both high porosity and specific surface area for biosensor design. We report here the preparation, characterization, and activity of a peptide-nanocellulose aerogel (PA) made from unprocessed cot...

  12. Production of cellulose phosphate from oil palm empty fruit bunch: Effect of chemical ratio

    Science.gov (United States)

    Rohaizu, R.; Wanrosli, W. D.

    2015-06-01

    Cellulose phosphate was synthesized from oil palm biomass residue that has the potential to represent a considerable added value product for the oil palm biomass utilization. Cellulose phosphate (CP) is prepared viaa phosphorylation process using the H3PO4/P2O5/Et3PO4/hexanol sequence using oil palm empty fruit bunch microcrystalline cellulose (OPEFB-MCC) as the starting material. Various factors affect its synthesis; one of them which is the subject of this investigation is the orthophosphoric acid (H3PO4) to triethylphosphate(Et3PO4) ratio which have the capability to increase the phosphorus content of CP. It is believed that during this reaction, the esterification of the free hydroxyl groups of the cellulose occurred. The H3PO4/Et3PO4 ratios applied were 0.16, 1.00, and 1.84. The effect of the H3PO4/Et3PO4 ratio on phosphorus content, yield, water swelling and molecular structure of CP are discussed.

  13. Preparation of microfibrillated cellulose/chitosan-benzalkonium chloride biocomposite for enhancing antibacterium and strength of sodium alginate films.

    Science.gov (United States)

    Liu, Kai; Lin, Xinxing; Chen, Lihui; Huang, Liulian; Cao, Shilin; Wang, Huangwei

    2013-07-03

    The nonantibacterial and low strength properties of sodium alginate films negatively impact their application for food packaging. In order to improve these properties, a novel chitosan-benzalkonium chloride (C-BC) complex was prepared by ionic gelation using tripolyphosphate (TPP) as a coagulant, and a biocomposite obtained through the adsorption of C-BC complex on microfibrillated cellulose, MFC/C-BC, was then incorporated into a sodium alginate film. The TEM image showed that the C-BC nanoparticles were spherical in shape with a diameter of about 30 nm, and the adsorption equilibrium time of these nanoparticles on the surface of MFC was estimated to be 6 min under the driving forces of hydrogen bonds and electrostatic interactions. According to the disc diffusion method, the MFC/C-BC biocomposite-incorporated sodium alginate film exhibited remarkable antibacterial activity against Staphylococcus aureus and certain antibacterial activity against Escherichia coli . The strength tests indicated that the tensile strength of the composite sodium alginate film increased about 225% when the loading of MFC/C-BC biocomposite was 10 wt %. These results suggested that the MFC/C-BC biocomposite-incorporated sodium alginate film with excellent antibacterial and strength properties would be a promising material for food packaging, and the MFC/C-BC may also be a potential multifunctional biocomposite for other biodegradable materials.

  14. Preparation of Superabsorbent Resin from Carboxymethyl Cellulose Grafted with Acrylic Acid by Low-temperature Plasma Treatment

    Directory of Open Access Journals (Sweden)

    Li Jie Huang

    2014-04-01

    Full Text Available A superabsorbent resin (SAR synthesized from carboxymethyl cellulose (CMC by grafting acrylic acid (AA was studied using single-factor analysis. The optimum preparation conditions were as follows: plasma discharge power of 250 W, processing time of 90 s, pressure of 300 Pa, m(CMC:m(AA ratio of 1:9, m(K2S2O8:m(CMC ratio of 1:4, and neutralization degree of 40%. Under these conditions, the resin has a salt water absorbency of 38.5 g/g and a stable chlorine dioxide solution absorbency of 27.2 g/g. The structural characterization of the SAR was also studied by Fourier transform infrared spectroscopy (FTIR, X-ray diffraction (XRD, scanning electron microscopy (SEM, and differential scanning colorimetry (DSC. The results showed that the resin was synthesized by grafting copolymerization of CMC and AA, and the water absorbency and thermal stability of the resin were greatly improved compared to CMC alone. This method may provide a new way for high value-added utilization of bagasse.

  15. Adsorption of Cr(VI) using cellulose microsphere-based adsorbent prepared by radiation-induced grafting

    Science.gov (United States)

    Li, Cancan; Zhang, Youwei; Peng, Jing; Wu, Hao; Li, Jiuqiang; Zhai, Maolin

    2012-08-01

    Cellulose microsphere (CMS) adsorbent was prepared by radiation-induced grafting of dimethylaminoethyl methacrylate (DMAEMA) onto CMS followed by a protonation process. The FTIR spectra analysis proved that PDMAEMA was grafted successfully onto CMS. The adsorption of Cr(VI) onto the resulting adsorbent was very fast, the equilibrium adsorption could be achieved within 15 min. The adsorption capacity strongly depended on the pH of the solution, which was attributed to the change of both the existed forms of Cr(VI) and the tertiary-ammonium group of PDMAEMA grafted CMS with the pH. A maximum Cr(VI) uptake (ca. 78 mg g-1) was obtained as the pH was in the range of 3.0-6.0. However, even in strong acid media (pH 1.3), the adsorbents still showed a Cr(VI) uptake of 30 mg g-1. The adsorption behavior of the resultant absorbent could be described with the Langmuir mode. This adsorbent has potential application for removing heavy metal ion pollutants (e.g. Cr(VI)) from wastewater.

  16. Manganese-containing cellulose nanocomposites: the restrain effect of cellulose treated with NaOH/urea aqueous solutions.

    Science.gov (United States)

    Ma, Ming-Guo; Deng, Fu; Yao, Ke

    2014-10-13

    In this article, the manganese-containing cellulose nanocomposites were obtained using microcrystalline cellulose and Mn(CH3COO)2 · 4H2O in the NaOH/urea aqueous solutions by a efficient microwave-assisted method. The effects of the heating time and Mn(CH3COO)2 · 4H2O concentration on the cellulose nanocomposites were investigated. It was found that the microcrystalline cellulose pretreated with NaOH/urea aqueous solutions played an important role in the phase, shape, and thermal stability of manganese-containing cellulose nanocomposites. Well-crystalline phases of manganese oxides were not observed in the manganese-containing cellulose nanocomposites. Furthermore, well-crystalline phases of manganese oxides were not also observed by thermal treatment of the manganese-containing cellulose nanocomposites at 600 °C for 3h. These results could be attributed to the restrain effect of cellulose treated with NaOH/urea aqueous solutions. It was supposed the possible mechanism during the phase transformation of cellulose nanocomposites.

  17. CHARACTERIZATION OF REGENERATED CELLULOSE MEMBRANES HYDROLYZED FROM CELLULOSE ACETATE

    Institute of Scientific and Technical Information of China (English)

    Yun Chen; Xiao-peng Xiong; Guang Yang; Li-na Zhang; Sen-lin Lei; Hui Lianga

    2002-01-01

    A series of cellulose acetate membranes were prepared by using formamide as additive, and then were hydrolyzedin 4 wt% aqueous NaOH solution for 8 h to obtain regenerated cellulose membranes. The dependence of degree ofsubstitution, structure, porous properties, solubility and thermal stability on hydrolysis time was studied by chemical titration,Fourier transform infrared spectroscopy, scanning electron microscopy, wide-angle X-ray diffraction, and differentialscanning calorimetry, respectively. The results indicated that the pore size of the regenerated cellulose membranes wasslightly smaller than that of cellulose acetate membrane, while solvent-resistance, crystallinity and thermostability weresignificantly improved. This work provides a simple way to prepare the porous cellulose membranes, which not only kept thegood pore characteristics of cellulose acetate membranes, but also possessed solvent-resistance, high crystallinity andthermostability. Therefore, the application range of cellulose acetate membranes can be expanded.

  18. Entrapment of cross-linked cellulase colloids in alginate beads for hydrolysis of cellulose.

    Science.gov (United States)

    Nguyen, Le Truc; Lau, Yun Song; Yang, Kun-Lin

    2016-09-01

    Entrapment of enzymes in calcium alginate beads is a popular enzyme immobilization method. However, leaching of immobilized enzymes from the alginate beads is a common problem because enzyme molecules are much smaller than the pore size of alginate beads (∼200nm). To address this issue, we employ a millifluidic reactor to prepare cross-linked cellulase aggregate (XCA) colloids with a uniform size (∼300nm). Subsequently, these colloids are immobilized in calcium alginate beads as biocatalysts to hydrolyze cellulose substrates. By using fluorescent microscopy, we conclude that the immobilized XCA colloids distribute uniformly inside the beads and do not leach out from the beads after long-term incubation. Meanwhile, the pore size of the alginate beads is big enough for the cellulose substrates and fibers to diffuse into the beads for hydrolysis. For example, palm oil fiber and microcrystalline cellulose can be hydrolyzed within 48h and release reducing sugar concentrations up to 2.48±0.08g/l and 4.99±0.09g/l, respectively. Moreover, after 10 cycles of hydrolysis, 96.4% of the XCA colloids remain inside the alginate beads and retain 67% of the original activity. In contrast, free cellulase immobilized in the alginate beads loses its activity completely after 10 cycles. The strategy can also be used to prepare other types of cross-linked enzyme aggregates with high uniformity. Copyright © 2016 Elsevier B.V. All rights reserved.

  19. Preparation and evaluation of gastroretentive floating pellets of metronidazole using Na-alginate and hydroxyl propyl methyl cellulose polymers.

    Science.gov (United States)

    Biswas, S K; Paul, S; Chowdhury, A; Das, J

    2012-03-15

    Gastroretentive floating pellets of metronidazole were formulated to prolong the gastric residence time in order to obtain controlled release characteristics of the drug. Nine formulations of metronidazole floating pellets such as AX, BX, CX, AY, BY, CY, AZ, BZ and CZ were prepared by extrusion method using different quantities of hydroxyl propyl methyl cellulose (HPMC) polymers such as methocel K4M premium and methocel K100LV premium in the ratio of 2:1, 1:2 and 1.5:1.5 while the amount of Na-alginate used in the formulations was 3.50, 5.25 and 7.0 g, respectively. The in vitro dissolution studies were carried out in 900 mL of phosphate buffer (pH 1.2) at 37 +/- 0.5 degrees C and 50 rpm for 6 h using USP XXIV paddle method and the content of drug release was done by UV spectrophotometer at 277 nm. It was found that the percent release of metronidazole from different formulations was different with passing of time. The drug release profile of the formulation (AX) having Na-alginate 3.50 g methocel K4M premium and methocel K100LV premium in the ratio of 2:1 showed best fit to Higuchi release kinetics with R2 value of 0.994. Finally, it might be concluded that the polymers had significant effect on drug release kinetics of metronidazole from floating pellets. The selection and use of suitable polymers in appropriate ratio might be very important in designing floating pellets and using the capabilities of these polymers, suitable floating pellets of metronidazole with desirable release rate could be formulated. Thus, in vivo research studies by the future researchers will confirm the appropriateness of these formulated metronidazole floating pellets.

  20. Physicochemical properties and mechanism of drug release from ethyl cellulose matrix tablets prepared by direct compression and hot-melt extrusion.

    Science.gov (United States)

    Crowley, Michael M; Schroeder, Britta; Fredersdorf, Anke; Obara, Sakae; Talarico, Mark; Kucera, Shawn; McGinity, James W

    2004-01-28

    The objective of this research project was to determine the physicochemical properties and investigate the drug release mechanism from ethyl cellulose (EC) matrix tablets prepared by either direct compression or hot-melt extrusion (HME) of binary mixtures of water soluble drug (guaifenesin) and the polymer. Ethyl cellulose was separated into "fine" or "coarse" particle size fractions corresponding to 325-80 and 80-30 mesh particles, respectively. Tablets containing 30% guaifenesin were prepared at 10, 30, or 50 kN compaction forces and extruded at processing temperatures of 80-90 and 90-110 degrees C. The drug dissolution and release kinetics were determined and the tablet pore characteristics, tortuosity, thermal properties and surface morphologies were studied using helium pycnometry, mercury porosimetry, differential scanning calorimetry and scanning electron microscopy. The tortuosity was measured directly by a novel technique that allows for the calculation of diffusion coefficients in three experiments. The Higuchi diffusion model, Percolation Theory and Polymer Free Volume Theory were applied to the dissolution data to explain the release properties of drug from the matrix systems. The release rate was shown to be dependent on the ethyl cellulose particle size, compaction force and extrusion temperature.

  1. Preparation and Application of Tripeptide-cellulose Ester%三肽纤维素酯的制备及应用研究

    Institute of Scientific and Technical Information of China (English)

    李杨; 朱进科; 李连杰; 蒋登高

    2016-01-01

    Tripeptide-cellulose ester ( TPC) was synthesized by sequent acyl chlorination, esterification, peptide elongation and amino modification using microcrystalline cellulose as raw material and N-(9-fluorenylmethoxycarbonyl)-L-proline(FMOC-L-Pro-OH), N-(9-fluorenylmethoxycarbonyl)-L-valinamide-L-phenylalanine(FMOC-L-Val-L-Phe-OH), 3,5-dinitrobenzoic acid as derivatization reagents. The experimental results showed that during the synthesis process, esterification, a key step, was performed firstly, and followed by the extension of peptide chain. The effects of various experimental factors on esterification and substitution degree ( DS ) were investigated. The optimal condition was described as that the mass concentration of avicel in LiCl/DMAc 20 g/L, the molar ratio of —C(O)Cl to the hydroxyl content of cellulose 3∶1, reaction temperature 100℃ and reaction time 20 h. By the further peptide elongation and amino modification, the tripeptide-cellulose ester with DS 2. 15 was synthesized. The structure and properties were then characterized by using Fourier transform infrared spectroscopy, elemental analysis, X-ray diffraction and thermogravimetric analysis. The results showed that the modification of peptide by 3,5-dinitrobenzoic acid was successful and the synthesis process was feasible. With the alteration of precipitants, the intramolecular hydrogen bond was different and the obtained derivatives had different characteristics and functionalities. The tripeptide-cellulose ester precipitated in methanol was good enteric-coating material with good shading effect and rapid disintegration, but the physiological toxicity needed further study. The tripeptide-cellulose ester ( using water as the precipitant) could be coated onto silica gel to get a chiral stationary phase, which has a wider application than previous coated-cellulose chiral stationary phase. In addition, the stable chemical resistance of tripeptide-cellulose ester was particularly suitable for the

  2. Supramolecular composite materials from cellulose, chitosan, and cyclodextrin: facile preparation and their selective inclusion complex formation with endocrine disruptors.

    Science.gov (United States)

    Duri, Simon; Tran, Chieu D

    2013-04-23

    We have successfully developed a simple one-step method of preparing high-performance supramolecular polysaccharide composites from cellulose (CEL), chitosan (CS), and (2,3,6-tri-O-acetyl)-α-, β-, and γ-cyclodextrin (α-, β-, and γ-TCD). In this method, [BMIm(+)Cl(-)], an ionic liquid (IL), was used as a solvent to dissolve and prepare the composites. Because a majority (>88%) of the IL used was recovered for reuse, the method is recyclable. XRD, FT-IR, NIR, and SEM were used to monitor the dissolution process and to confirm that the polysaccharides were regenerated without any chemical modifications. It was found that unique properties of each component including superior mechanical properties (from CEL), excellent adsorption for pollutants and toxins (from CS), and size/structure selectivity through inclusion complex formation (from TCDs) remain intact in the composites. Specifically, the results from kinetics and adsorption isotherms show that whereas CS-based composites can effectively adsorb the endocrine disruptors (polychlrophenols, bisphenol A), their adsorption is independent of the size and structure of the analytes. Conversely, the adsorption by γ-TCD-based composites exhibits a strong dependence on the size and structure of the analytes. For example, whereas all three TCD-based composites (i.e., α-, β-, and γ-TCD) can effectively adsorb 2-, 3-, and 4-chlorophenol, only the γ-TCD-based composite can adsorb analytes with bulky groups including 3,4-dichloro- and 2,4,5-trichlorophenol. Furthermore, the equilibrium sorption capacities for the analytes with bulky groups by the γ-TCD-based composite are much higher than those by CS-based composites. Together, these results indicate that the γ-TCD-based composite with its relatively larger cavity size can readily form inclusion complexes with analytes with bulky groups, and through inclusion complex formation, it can strongly adsorb many more analytes and has a size/structure selectivity compared to

  3. Predictive screening of ionic liquids for dissolving cellulose and experimental verification

    DEFF Research Database (Denmark)

    Liu, Yanrong; Thomsen, Kaj; Nie, Yi

    2016-01-01

    In this work, 357 ionic liquids (ILs) formed from 17 cations and 21 anions were selected for evaluation of their ability to dissolve cellulose by COSMO-RS. In order to evaluate the predictive model and method, experimental measurements of the solubility of microcrystalline cellulose (MCC) in 7...... results than a neat glucose model and the model of the mid-dimer part of cellotetraose. Excess enthalpy calculations indicated that hydrogen-bond (H-bond) interactions between cellulose (i.e. the three cellulose models) and the 7 studied ILs are key factors for the solubility of cellulose, and the anions...

  4. The magnetic properties of powdered and compacted microcrystalline permalloy

    Science.gov (United States)

    Kollár, P.; Olekšáková, D.; Füzer, J.; Kováč, J.; Roth, S.; Polański, K.

    2007-03-01

    The aim of this work is to investigate the magnetic properties of powdered and compacted microcrystalline Ni-Fe (81 wt% of Ni) permalloy. It was found by investigating the influence of mechanical milling on the magnetic properties of powder samples prepared by milling of the ribbon that the alloy remains a solid solution with stable structure during the whole milling process. With decreasing particle size the rotation of magnetization vector gradually becomes dominant magnetization process and thus coercivity increases. After compaction of the powder by uniaxial hot pressing the magnetic contact between powder particles is recreated and for resulting bulk the displacement of the domain walls becomes dominant magnetization process with coercivity of 11 A/m (comparable with the coercivity of conventional permalloy).

  5. A novel, cost-effective and eco-friendly method for preparation of textile fibers from cellulosic pulps.

    Science.gov (United States)

    Alam, Md Nur; Christopher, Lew P

    2017-10-01

    Although cellulosic fibers are increasingly used in textile products, current methods for production of cellulose-based textiles suffer certain economic and/or environmental drawbacks. We have developed a new, cost-effective and environmentally-friendly (CS2-free) process that overcomes some of the shortcomings of existing technologies. The process is based on a modified method for periodate oxidation of cellulose that is then cross-linked with chitosan and extruded to obtain cellulosic fibers in the form of textile fibers. The produced fibers have low content of aldehyde groups (∼2mmol/g cellulose) and water retention values of 1.5-2.0g/g fibers. The new process makes use of both hardwood and softwood pulps, and offers significant yield advantages over the use of dissolving pulp as a raw material. The mechanical, water absorbency and morphological properties of the new textile fibers and their potential applications are discussed. The potential techno-economic and environmental benefits of the process are summarized. Copyright © 2017 Elsevier Ltd. All rights reserved.

  6. Preparation of Cellulosic Membrane Containing Pyrrolidone Moiety Via Radiation Induced Grafting and its Application in Wastewater Treatment

    Directory of Open Access Journals (Sweden)

    A. S. Aly

    2005-01-01

    Full Text Available Radiation induced grafting of vinyl pyrrolidone onto cellulose wood pulp was carried out in heterogeneous and homogenous media using gamma radiation. Cellulose wood pulp was used in different forms; a in a homogenous solution by dissolving the wood pulp in N,N- dimethylacetamide/Lithium chloride (DMAc/LiCl mixture , b in a membrane form, by precipitating the cellulose solution in water and c in a powder form. Factors affecting on the grafting such as radiation dose, monomer concentration, precipitator concentration and thickness of the membrane have been studied. The result showed that at the same dose, the grafting yield was higher with cellulose in soluble form than in the membrane form, whereas cellulose in powder exhibited the lowest graft yield. The grafted membrane was characterized by IR, TGA and SEM. The ability of the grafted membrane to remove dyes (acid and basic dye, heavy metal ions (Co 2+ , Ni 2+ and Cu 2+ and phenols from wastewater was also reported.

  7. Study on the Preparation and Properties of Crease Resistant Cellulose Fiber%防皱纤维素纤维的制备与性能研究1

    Institute of Scientific and Technical Information of China (English)

    刘杰; 朱平; 刘帅; 董朝红; 隋淑英; 张林

    2016-01-01

    采用离子液体溶解纤维素浆粕、免烫整理剂1,2,3,4-丁烷四羧酸(BTCA)及催化剂次亚磷酸钠(SHP)制备纺丝液,湿法纺丝,弱酸凝固浴中再生,经预烘、焙烘制备交联再生纤维素纤维,红外光谱测试结果证明了BTCA交联再生纤维素纤维制备成功;探讨了影响交联纤维折痕回复性能、湿强及湿模量的因素,得到BTCA交联再生纤维素纤维制备的最佳工艺条件,交联后纤维干湿折痕回复角较原再生纤维素纤维分别提高了76.4%与41.1%,且耐水洗性优良。%The cellulose pulp, durable press finishing agent BTCA and catalytic agent SHP was dissolved in ionic liquid. The as-spun fiber was prepared by wet spinning method. The cross-linked regenerated cellulose fiber was prepared after the as-spun fiber was precured and then cured. The cross-linked regenerated cellulose fiber was proved to be successfully prepared by FT-IR tests. The influence factors of wrinkle recovery property, wet strength and wet modulus of the fiber were investigated. The optimum conditions of the cross-linked fiber were obtained. The dry and wet crease recovery angle of cross-linked fiber was improved by 76.4% and 41.4%, separately. Furthermore, the washing durability of the cross-linked fiber was excellent.

  8. Preparation and application of nanocrystalline cellulose derived from sugarcane waste as filler modified alkanolamide on crosslink of natural rubber latex film

    Science.gov (United States)

    Harahap, Hamidah; Hayat, Nuim; Lubis, Marfuah

    2017-07-01

    Sugarcane waste is abundant sources of cellulose and it has potential to reutilize. Cellulose from sugarcane waste can be derived into nanocystalline cellulose (NCC) from crystalline region. The NCC as a filler has capability to reinforce natural rubber latex product. The crosslink in vulcanized natural rubber latex film influences several properties of product. In this work, we extracted NCC from sugarcane waste then added into natural rubber latex as filler modified alkanolamide (ALK) and also studied the crosslink of natural rubber latex films. NCC were produced from sugarcane waste by hydrolysis process with sulfuric acid 45%. The obtained NCC was characterized by using x-ray diffraction (XRD), transmission electron microscopy (TEM), and fourier transform infra red (FTIR). NCC was modified by alkanolamide and dispersed in water with filler concentration of 10%. Then the dispersion were added into latex system followed by pre-vulcanization at 70 °C. The films were prepared by coagulant dipping method and dried at 100 °C and 120 °C for 20 minutes. Characterization of NCC from sugarcane waste by using FTIR was done, it clearly showed the functional groups of cellulose. TEM showed the obtained NCC were rod-shaped with about 40-160 nm in diameter and several hundred nm in length, and XRD showed that the degree of crystalinity of NCC from sugarcane waste is 92.33%. The crosslink of natural rubber films were studied by measure the crosslink density for different filler loading by using swelling measurement with toluene solution. The result show that the crosslink density increased in line with amount of filler which added into the system, and also the crosslink density that obtained from vulcanization at 120 °C were higher than 100 °C.

  9. NanoCrystalline Cellulose, an environmental friendly nanoparticle for pharmaceutical application – A quick study

    Directory of Open Access Journals (Sweden)

    Song Yee Kai

    2016-01-01

    Full Text Available Nanocrystalline cellulose (NCC is probably the most abundant nano material can be found in nature. It offers not only substantial environmental advantage due to its intrinsic biocompatibility and biodegradability, but also outstanding aspect ratio, tension modulus, bioavailability and permeability. NCC can be isolated from low value biomass through a well-developed acid hydrolysis method, and the structure can be readily manipulated during extraction to obtain desirable size distribution, surface charge and degree of crystallinity. Erratic absorption of drug has been a major issue for years until the emergence of nanoparticle adopted as smart vehicle for drug delivery. However, due to inevitably severe toxicity and the side effect from ordinary nanoparticle, the exploration of green nanoparticles are catching escalating attention is now in urge. Microcrystalline cellulose (MCC has long been an option, nevertheless, due to their relatively low surface charge compared to total volume, drug release in a control manner was hardly satisfied. It is suggested that the above limitation can be overcome by nanocrystalline cellulose. This article discusses and explores their potential in cosmetic, personal care and pharmaceutical application, and the recent development in term of preparation and characteristic.

  10. Sulfonated hierarchical H-USY zeolite for efficient hydrolysis of hemicellulose/cellulose.

    Science.gov (United States)

    Zhou, Lipeng; Liu, Zhen; Shi, Meiting; Du, Shanshan; Su, Yunlai; Yang, Xiaomei; Xu, Jie

    2013-10-15

    Sulfonated hierarchical H-USY zeolite was prepared and characterized by X-ray diffraction, N2 physisorption, Fourier transform infrared spectroscopy, inductively coupled plasma atomic emission spectroscopy, temperature-programmed desorption of ammonia, and acid-base titration. It was proved that sulfonic group was successfully anchored onto the hierarchical H-USY zeolite. The acidity of the hierarchical H-USY was remarkably improved. Sulfonated hierarchical H-USY zeolite was efficient for the hydrolysis of hemicellulose and cellulose. The yield of TRS for hydrolysis of hemicellulose reached 78.0% at 140 °C for 9h. For hydrolysis of α-cellulose, 60.8% conversion with 22.4% yield of glucose was obtained. Even for microcrystalline cellulose, 43.7% conversion with 15.1% yield of glucose can be obtained. These results are much higher than those obtained over hierarchical H-USY zeolite, indicating that both the acidity and the pore structure determine the activity of zeolite as catalyst in the hydrolysis of biomass. Copyright © 2013 Elsevier Ltd. All rights reserved.

  11. Cellulose nanocrystal/polyolefin biocomposites prepared by solid-state shear pulverization: Superior dispersion leading to synergistic property enhancements

    Science.gov (United States)

    Krishnan A. Iyer; Gregory T. Schueneman; John M. Torkelson

    2015-01-01

    Cellulose nanocrystals (CNCs), a class of renewable bionanomaterials with excellent mechanical properties, have gained major interest as filler for polymers. However, challenges associated with effective CNC dispersion have hindered the production of composites with desired property enhancements. Here, composites of polypropylene (PP) and low density polyethylene (LDPE...

  12. Study on Mechanical Properties of Micro-crystalline Cellulose Reinforced Polypropylene Composites and Its Preparation%微晶纤维素增强聚丙烯复合材料的制备与力学性能研究

    Institute of Scientific and Technical Information of China (English)

    王兆礼; 赵升云; 龚新怀; 赵缙云

    2016-01-01

    以聚丙烯(PP)为基体、微晶纤维素(MCc)为增强材料、马来酸酐接枝聚丙烯(PP-g-MA)为相容剂,利用双螺杆挤出机制备了PP/MCC/PP-g-MA复合材料,同时研究了该复合材料的力学性能.随后分别选用三元乙丙橡胶(EPDM)和乙烯-辛烯共聚物(POE)对PP/MCC/PP-g-MA复合材料进行增韧改性,考察了两种增韧剂的增韧效果.结果表明:加入PP-g-MA后,PP/MCC复合材料的力学性能明显提高.另外,增韧剂的引入使PP/MCC/PP-g-MA复合材料的冲击性能显著改善,其中POE对复合材料的增韧效果优于EPDM.但是增韧剂的引入会造成复合材料的拉伸强度、弹性模量和弯曲强度分别出现不同程度的下降,其中EPDM增韧复合材料的上述性能下降幅度相对较小.

  13. Microcrystalline coatings deposited by series double-pole electro-pulse discharge and its high-temperature oxidation behavior

    Institute of Scientific and Technical Information of China (English)

    徐强; 何业东; 王德仁; 齐慧滨; 李正伟; 高唯

    2002-01-01

    A new technique--series electro-pulse discharge (SEPD)--was developed as a surface coating process. In this process, both positive and negative poles of a pulse power were used as the depositing electrodes and the substrate alloy was used as an induction electrode. The physical process for such SEPD was tested by measuring the relationship between the discharge voltages and gaps in a pin-plate-pin system. Microcrystalline Ni20Cr alloy coatings and oxide- dispersed Ni20Cr alloy coatings were prepared on Ni20Cr alloy surface by using a vibrating SEPD device. Oxidation at 950℃ in ambient air showed that the microcrystalline Ni20Cr alloy coatings greatly improved the oxidation resistance of the substrate alloy. The addition of dispersed Y2O3 nano-particles into the microcrystalline coatings was found to further reduce the oxidation rate and enhance the oxide spallation resistance.

  14. Method for the preparation of cellulose acetate flat sheet composite membranes for forward osmosis—Desalination using MgSO4 draw solution

    KAUST Repository

    Sairam, M.

    2011-06-01

    A lab scale method for the preparation of defect free flat sheet composite membranes for forward osmosis (FO) has been developed. Membranes containing a thin layer of cellulose acetate (CA) cast on a nylon fabric of 50μm thick were prepared by phase inversion in water. Cellulose acetate (CA) membranes with an overall thickness of 70-80μm have been prepared with lactic acid, maleic acid and zinc chloride as pore forming agents, at different annealing temperatures, for forward osmosis. These membranes have been tested in the desalination of saline feeds (35g·L-1 of NaCl) using magnesium sulphate solution (150g·L-1) as the draw solution. The water flux, and rejection of NaCl, were compared with those of commercially available membranes tested under the same FO conditions. The commercially available FO membrane from Hydration Technologies Inc, OR (M1) has a permeability of 0.13L·h-1·m-2·bar-1 with a NaCl rejection of 97% when tested with 150g·L-1 of MgSO4 in the draw solution. Another commercially available membrane for FO from Hydration Technologies Inc, OR, M2 has a water permeability of 0.014L·h-1·m-2·bar-1 with NaCl rejection of 100%. The flux and rejection of the CA membranes prepared in this work are found to be dependent on the nature of the pore forming agent, and annealing temperature. Impregnation of an inorganic filler, sodium montmorrillonite in CA membranes and coating of CA membranes with hydrophilic PVA did not enhance the flux of base CA membranes. Cellulose acetate membranes cast from dope solutions containing acetone/isopropanol and lactic acid, maleic acid and zinc chloride as pore forming agents have water permeabilities of 0.13, 0.09 and 0.68L·h-1·m-2·bar-1 respectively, with NaCl rejections of 97.7, 99.3 and 88% when annealed at 50°C. CA membranes prepared with zinc chloride as a pore forming agent have good permeability of 0.27L·h-1·m-2·bar-1 with a NaCl rejection of 95% when annealed at 70°C. © 2011.

  15. Preparation and Characterization in vitro of Sustained-release Captopril/Chitosan-gelatin Net-polymer Microspheres(Cap/CGNPMs)

    Institute of Scientific and Technical Information of China (English)

    SONG Yimin; CHEN Xiguang; TANG Xuexi; LIU Chengshen; MENG Xianghong; YU Luojun

    2006-01-01

    The captopril/Chitosan-gelatin net-polymer microspheres (Cap/CGNPMs) were prepared using Chitosan(CS) and gelatin(Gel) by the methods of emulsification. A cross linked reagent alone or in combination with microcrystalline cellulose(MCC) was added in the process of preparation of microspheres to eliminate dose dumping and burst phenomenon of microspheres for the improvement of the therapeutic efficiency and the decrease of the side effects of captopril(Cap). The results indicate that Cap/CGNPMs have a spherical shape , smooth surface morphology and integral inside structure and no adhesive phenomena and good mobility,and the size distribution is mainly from 220 to 280 μm. Researches on the Cap release test in vitro demonstrate that Cap/CGNPMs are of the role of retarding release of Cap compared with Cap ordinary tablets (COT), embedding ratio (ER) ,drug loading (DL), and swelling ratio (SR), and release behaviors of CGNPMS are influenced by process conditions of preparation such as experimental material ratio (EMR) , composition of cross linking reagents. Among these factors , the EMR(1/4),CLR (FOR+TPP) and 0.75% microcrystalline cellulose (MCC) added to the microspheres are the optimal scheme to the preparation of Cap/CGNPMs. The Cap/CGNPMs have a good characteristic of sustained release of drug, and the process of emulsification and cross-linking process is simple and stable. The CGNPMs is probable to be one of an ideal sustained release system for water-soluble drugs.

  16. A fast method to diagnose phase transition from amorphous to microcrystalline silicon

    Institute of Scientific and Technical Information of China (English)

    HOU; GuoFu

    2007-01-01

    A series of hydrogenated silicon thin films were prepared by the radio frequency plasma enhanced chemical vapor deposition method (RF-PECVD) with various silane concentrations. The influence of silane concentration on structural and electrical characteristics of these films was investigated to study the phase transition region from amorphous to microcrystalline phase. At the same time, optical emission spectra (OES) from the plasma during the deposition process were monitored to get information about the plasma properties, Raman spectra were measured to study the structural characteristics of the deposited films. The combinatorial analysis of OES and Raman spectra results demonstrated that the OES can be used as a fast method to diagnose phase transition from amorphous to microcrystalline silicon. At last the physical mechanism, why both OES and Raman can be used to diagnose the phase transition, was analyzed theoretically.……

  17. Employing ionic liquids to deposit cellulose on PET fibers.

    Science.gov (United States)

    Textor, Torsten; Derksen, Leonie; Gutmann, Jochen S

    2016-08-01

    Several ionic liquids are excellent solvents for cellulose. Starting from that finishing of PET fabrics with cellulose dissolved in ionic liquids like 1-ethyl-3-methyl imidazolium acetate, diethylphosphate and chloride, or the chloride of butyl-methyl imidazolium has been investigated. Finishing has been carried out from solutions of different concentrations, using microcrystalline cellulose or cotton and by employing different cross-linkers. Viscosity of solutions has been investigated for different ionic liquids, concentrations, cellulose sources, linkers and temperatures. Since ionic liquids exhibit no vapor pressure, simple pad-dry-cure processes are excluded. Before drying the ionic liquid has to be removed by a rinsing step. Accordingly rinsing with fresh ionic liquid followed by water or the direct rinsing with water have been tested. The amount of cellulose deposited has been investigated by gravimetry, zinc chloride iodine test as well as reactive dyeing. Results concerning wettability, water up-take, surface resistance, wear-resistance or washing stability are presented.

  18. Cellulose extraction from Zoysia japonica pretreated by alumina-doped MgO in AMIMCl.

    Science.gov (United States)

    Liu, Le; Ju, Meiting; Li, Weizun; Jiang, Yang

    2014-11-26

    In this study, alumina-doped MgO was produced as a solid alkali for lignocellulose pretreatment. Pretreatment with alumina-doped MgO disrupted the lignocellulose structure and significantly reduced the lignin content of the Z. japonica. After pretreatment, Z. japonica showed significant solubility in 1-allyl-3-methylimidazolium chloride (AMIMCl). The similar high solubility of pretreated Z. japonica samples by original alumina-doped MgO and used alumina-doped MgO also proved that alumina-doped MgO had strong stability, which can be recycled and used repeatedly. The regenerated cellulose was similar to microcrystalline cellulose according to FTIR and NMR analyses. Compared to microcrystalline cellulose, only the crystallinity of the regenerated cellulose decreased.

  19. Effect of hydrolysed cellulose nanowhiskers on properties of montmorillonite/polylactic acid nanocomposites.

    Science.gov (United States)

    Arjmandi, Reza; Hassan, Azman; Haafiz, M K M; Zakaria, Zainoha; Islam, Md Saiful

    2016-01-01

    Polylactic acid (PLA) nanocomposites reinforced with hybrid montmorillonite/cellulose nanowhiskers [MMT/CNW(SO4)] were prepared by solution casting. The CNW(SO4) nanofiller was first isolated from microcrystalline cellulose using acid hydrolysis treatment. PLA/MMT/CNW(SO4) hybrid nanocomposites were prepared by the addition of various amounts of CNW(SO4) [1-9 parts per hundred parts of polymer (phr)] into PLA/MMT nanocomposite at 5 phr MMT content, based on highest tensile strength values as reported previously. The biodegradability, thermal, tensile, morphological, water absorption and transparency properties of PLA/MMT/CNW(SO4) hybrid nanocomposites were investigated. The Biodegradability, thermal stability and crystallinity of hybrid nanocomposites increased compared to PLA/MMT nanocomposite and neat PLA. The highest tensile strength of hybrid nanocomposites was obtained by incorporating 1 phr CNW(SO4) [∼ 36 MPa]. Interestingly, the ductility of hybrid nanocomposites increased significantly by 87% at this formulation. The Young's modulus increased linearly with increasing CNW(SO4) content. This is due to the relatively good dispersion of nanofillers in the hybrid nanocomposites, as revealed by transmission electron microscopy. Fourier transform infrared spectroscopy indicated the formation of some polar interactions. In addition, water resistance of the hybrid nanocomposites improved and the visual transparency of neat PLA film did not affect by addition of CNW(SO4).

  20. Preparation and characterization of carboxymethyl cellulose from mechanically activated bagasse cellulose%机械活化甘蔗渣制备羧甲基纤维素及性能表征

    Institute of Scientific and Technical Information of China (English)

    陈渊; 韦庆敏; 杨家添; 朱万仁; 余桂英; 黄祖强

    2015-01-01

    type of CMC for specific user are becoming the development directions of CMC. Sugarcane bagasse (SCB), a kind of waste in the process of sugar extraction, is abundant and low-cost lignocelullosic material. SCB is mainly composed of cellulose, hemicellulose and lignin. Cellulose forms microfibril by intramolecular and intermolecular hydrogen bond, and hemicellulose and lignin are filling and adhering agent among the microfibril. Because of the special structure of SCB, chemical agents are difficult to penetrate and diffuse in it, which limits its application. Therefore, it is necessary to pretreat SCB to remove lignin and hemicellulose, reducing cellulose’s crystallinity. To utilize SCB and prepare CMC with high degree of substitution (DS), SCB was mechanically activated by a stirring-type ball mill. Using monochloroacetate (MCA) as etherifying agent and sodium hydroxide (NaOH) as catalyst, CMC was synthesized from SCB with different activation time. The effects of mechanical activation time, reaction time, reaction temperature, solid-liquid ratio, NaOH-MCA molar ratio and water content on carboxymethylation of SCB were investigated respectively by using the DS of CMC as evaluating parameter. The structure of CMC from SCB was characterized by using Fourier transform infrared spectroscopy (FTIR),X-ray diffraction (XRD) and 1HNMR spectroscopy (1HNMR). The results indicated that mechanical activation considerably enhanced the carboxymethylation of SCB, the mechanically activated SCB was easier for carboxymethylation than the original SCB, and the DS increased first and then decreased with activation time. The reasons were that mechanical activation broke the sealing of cellulose by lignin, destroyed the crystalline structure and decreased the crystallinity of cellulose, which made etherification reagent more easily penetrate into the SCB and could increase reactivity and decrease the dependence on solid-liquid ratio, ratio of NaOH/MCA, H2O/substrate, reaction time and

  1. Mercerization and Enzymatic Pretreatment of Cellulose in Dissolving Pulps

    OpenAIRE

    2013-01-01

    This thesis deals with the preparation of chemically and/or enzymatically modified cellulose. This modification can be either irreversible or reversible. Irreversible modification is used to prepare cellulose derivatives as end products, whereas reversible modification is used to enhance solubility in the preparation of regenerated cellulose. The irreversible modification studied here was the preparation of carboxymethyl cellulose (CMC) using extended mercerization of a spruce dissolving pulp...

  2. 农作物与其剩余物制备纳米纤维素研究进展%Research Progress of Nanocrystalline Cellulose Prepared from Crops and Agricultural Residues

    Institute of Scientific and Technical Information of China (English)

    宋孝周; 吴清林; 傅峰; 郭康权

    2011-01-01

    简要介绍了农业纤维主要组成成分,从原料种类、制备方法、纳米纤维素的性质及应用4个方面综述了利用农作物及其剩余物制备纳米纤维素的国内外研究进展.深入分析了利用农作物及其剩余物制备纳米纤维素在尺寸表征、表面改性、制备工艺及应用方面存在的主要问题及解决思路,为农作物及其剩余物的高值化应用提供参考.%The preparation of nanocrystalline cellulose using crops and agricultural residues has attracted wide attention recently. The primary composition of agricultural fibers was introduced. Research progress of nanocrystalline cellulose prepared from crops and agricultural residues was reviewed in terms of raw material kinds, preparation method, properties and application of nanocrystalline cellulose. The main problems in terms of dimensional measurement, surface modification, preparation technology and application were analyzed. The corresponding solution ways were put forward. The preparation of nanocrystalline cellulose is a high value-added application for crops and agricultural residues.

  3. Deconvolution Method for Determination of the Nitrogen Content in Cellulose Carbamates

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Cellulose carbamates (CC) were synthesized with microcrystalline cellulose as raw materials. The Fourier transform infrared spectra of CC with different nitrogen content were recorded. The accurate results of the nitrogen content for CC can be obtained by using the deconvolution method when the nitrogen content is less than 3.5%. The relationship between the nitrogen content and the absorption intensity ratio of the corresponding separated absorption peaks in FTIR spectra has been expressed by an equation precisely.

  4. Cellulose nanocrystals' production in near theoretical yields by 1-butyl-3-methylimidazolium hydrogen sulfate ([Bmim]HSO4)-mediated hydrolysis.

    Science.gov (United States)

    Mao, Jia; Heck, Barbara; Reiter, Günter; Laborie, Marie-Pierre

    2015-03-06

    We report on near theoretical yield production of cellulose I nanocrystals (CNCs) using a two-step hydrolysis with the mildly acidic ionic liquid (IL) 1-butyl-3-methylimidazolium hydrogen sulfate ([Bmim]HSO4) in aqueous solution from common cellulosic sources. Two successive Taguchi experimental plans were performed to evaluate the impact of selected reaction parameters (T, t, H2O:IL ratio) and their interactions on the CNCs' yield from bleached softwood kraft pulp (SWP), bleached hardwood kraft pulp (HWP) and microcrystalline cellulose (MCC). With these experimental plans, the molar yield for extraction of nanocrystals was optimized to near theoretical levels, reaching 57.7±3.0%, 57.0±2.0%, and 75.6±3.0%, for SWP, HWP and MCC, respectively. The reaction yields corresponded to a relative crystalline region recovery of 84.1±5.3%, 71.7±1.3%, 76.0±2.0% from SWP, HWP and MCC, respectively. The collected nanocrystals exhibited high aspect ratios (36-43), negligible sulfur content (0.02-0.21%) and high solvent dispersibility in comparison to those obtained with the traditional sulfuric acid method. Additionally these near theoretical yields were achieved for mild reaction conditions with the combined severity factor of 2 and 3 for MCC and pulp, respectively. Overall this two-stage IL-mediated preparation of nanocrystals combines the advantages of achieving high product quality, high reaction yields and mild conditions.

  5. Preparation and evaluation of gastroretentive floating tablets of acyclovir.

    Science.gov (United States)

    Garg, Rajeev; Gupta, G D

    2009-10-01

    The present study performed by preparation and evaluation of floating tablets of Acyclovir as model drug for prolongation of gastric residence time. Floating effervescent tablets were formulated by various materials like hydroxypropyl methylcellulose K 4M, K 15M, psyllium husk, swelling agent as crospovidone and microcrystalline cellulose and gas generating agent like sodium bicarbonate and citric acid and evaluated for floating properties, swelling characteristics and in vitro drug release studies. Floating noneffervescent tablets were prepared by polypropylene foam powder and different matrix forming polymers like HPMC K 4M, Carbopol 934P, xanthan gum and sodium alginate. In vitro drug release studies were performed and drug release kinetics evaluated using the linear regression method was found to follow both the Higuchi and the Korsmeyer and Peppas equation. The drug release mechanism was found fickian type in most of the formulations.

  6. Model films of cellulose. I. Method development and initial results

    NARCIS (Netherlands)

    Gunnars, S.; Wågberg, L.; Cohen Stuart, M.A.

    2002-01-01

    This report presents a new method for the preparation of thin cellulose films. NMMO (N- methylmorpholine- N-oxide) was used to dissolve cellulose and addition of DMSO (dimethyl sulfoxide) was used to control viscosity of the cellulose solution. A thin layer of the cellulose solution is spin- coated

  7. Preparation and Determination of Drug-Polymer Interaction and In-vitro Release of Mefenamic Acid Microspheres Made of CelluloseAcetate Phthalate and/or Ethylcellulose Polymers

    Science.gov (United States)

    Jelvehgari, Mitra; Hassanzadeh, Davoud; Kiafar, Farhad; Delf Loveym, Badir; Amiri, Sara

    2011-01-01

    The objective of this study was to formulate and evaluate the drug-polymer interaction of mefenamic acid (MA) using two polymers with different characteristics as ethylcellulose (EC) and/or cellulose acetate phthalate (CAP). Microspheres were prepared by the modified emulsion solvent evaporation (MESE). The effect of drug-polymer interaction was studied for each of microspheres. Important parameters in the evaluation of a microencapsulation technique are encapsulation efficiency, yield production, particle size, surface characteristics of microspheres, scanning electronic microscopy (SEM), powder X-ray diffraction analysis (XRD), and differential scanning calorimetry (DSC). The in-vitro release studies are performed in Tris buffer (pH 9) with Sodium lauryl sulfate (SLS). Microspheres containing CAP and EC showed 68-97% and 63-76% of entrapment efficiency, respectively. The thermogram X-ray and DSC showed stable character of MA in the microspheres and revealed an absence of drug polymer interaction. The prepared microspheres were spherical in shape and had a size range of 235-436 μm for CAP-microspheres and 358-442 μm for EC-microspheres. The results suggest that MA was successfully and efficiently encapsulated; the release rates of matrix microspheres are related to the type of polymer, only when polymers (EC and CAP combine with 1 : 1 ratio) were used to get prolonged drug release with reducing the polymers content in the microspheres. Data obtained from in-vitro release for microspheres and commercial capsule were fitted to various kinetic models and the high correlation was obtained in the peppas model. Mefenamic acid, Ethylcellulose, Cellulose acetate phthalate, Microparticles, Modified emulsion-solvent evaporation. PMID:24250377

  8. Observation of a microcrystalline gel in colloids with competing interactions.

    Science.gov (United States)

    Zhang, Tian Hui; Groenewold, Jan; Kegel, Willem K

    2009-12-14

    A stable short-range crystalline structure is observed in colloidal systems with competing short-range attractions and long-range repulsions. We term these structures "microcrystalline gels" as the microcrystals are embedded in a dense disordered network.

  9. Cellulose aerogels decorated with multi-walled carbon nanotubes: preparation, characterization, and application for electromagnetic interference shielding

    Directory of Open Access Journals (Sweden)

    Jian LI,Caichao WAN

    2015-12-01

    Full Text Available Electromagnetic wave pollution has attracted extensive attention because of its ability to affect the operation of electronic machinery and endanger human health. In this work, the environmentally-friendly hybrid aerogels consisting of cellulose and multi-walled carbon nanotubes (MWCNTs were fabricated. The aerogels have a low bulk density of 58.17 mg·cm-3. The incorporation of MWCNTs leads to an improvement in the thermal stability. In addition, the aerogels show a high electromagnetic interference (EMI SEtotal value of 19.4 dB. Meanwhile, the absorption-dominant shielding mechanism helps a lot to reduce secondary radiation, which is beneficial to develop novel eco-friendly EMI shielding materials.

  10. Preparation, characterization and thermal studies of polymer inclusion cellulose acetate membrane with calix[4]resorcinarenes as carriers

    Energy Technology Data Exchange (ETDEWEB)

    Benosmane, Nadjib [Laboratoire de Chimie Organique Appliquee (Groupe Heterocycles Associe CRAPC), Faculte de Chimie, Universite des Sciences et de la Technologie Houari Boumediene, BP 32, El-Alia, 16111 Bab-Ezzouar, Alger (Algeria); Guedioura, Bouzid [Division reacteur/Centre de Recherche Nucleaire de Draria, CRND, BP 43 Draria, Alger (Algeria); Hamdi, Safouane Mohammed [Laboratoire de Biochimie-Purpan, Institut Federatif de Biologie, CHU Toulouse 330, avenue de Grande-Bretagne - F-31059 Toulouse Cedex 9 (France); Hamdi, Maamar [Laboratoire de Chimie Organique Appliquee (Groupe Heterocycles Associe CRAPC), Faculte de Chimie, Universite des Sciences et de la Technologie Houari Boumediene, BP 32, El-Alia, 16111 Bab-Ezzouar, Alger (Algeria); Boutemeur, Baya, E-mail: bayakheddis@hotmail.com [Laboratoire de Chimie Organique Appliquee (Groupe Heterocycles Associe CRAPC), Faculte de Chimie, Universite des Sciences et de la Technologie Houari Boumediene, BP 32, El-Alia, 16111 Bab-Ezzouar, Alger (Algeria)

    2010-07-20

    A polymer inclusion membrane (PIM) system with cellulose acetate polymer as support and calix[4]resorcinarenes as carriers has been developed. Special attention was paid to PIM characterization using scanning electron microscopy, Fourier-transform infra-red study, X-ray scattering and thermogravimetric analyses. The efficiency of the membrane transport was optimized as a function of pH, stirring speed, aqueous phases and membrane composition. The results suggested that the transport mechanism is a counter-transport of protons, the mechanism was mainly controlled by the diffusion of the complex formed in the membrane core. Analysis of lead(II) transport through these PIMs was performed. It was found that calix[4]resorcinarenes containing membranes were flexible, resistant and heterogeneous without plasticizer addition.

  11. Ambipolar characteristics of microcrystalline silicon thin-film transistors

    Energy Technology Data Exchange (ETDEWEB)

    Chan, Kah-Yoong [IEF5-Photovoltaics, Research Center Juelich, 52425 Juelich (Germany); School of Engineering and Science, Jacobs University Bremen, 28759 Bremen (Germany); Faculty of Engineering, Multimedia University, 63100 Cyberjaya, Selangor (Malaysia); Gordijn, Aad [IEF5-Photovoltaics, Research Center Juelich, 52425 Juelich (Germany); Stiebig, Helmut [IEF5-Photovoltaics, Research Center Juelich, 52425 Juelich (Germany); Malibu GmbH and Co. KG, 33609 Bielefeld (Germany); Knipp, Dietmar [School of Engineering and Science, Jacobs University Bremen, 28759 Bremen (Germany)

    2010-04-15

    Hydrogenated microcrystalline silicon ({mu}c-Si:H) has recently attracted significant attention as a promising candidate for thin-film transistors (TFTs) in large-area electronics due to high electron and hole charge carrier mobilities. We report on top-gate ambipolar TFTs based on {mu}c-Si:H prepared by plasma-enhanced chemical vapor deposition at temperatures below 200 C. Electrons and holes are directly injected into the {mu}c-Si:H channel via chromium drain and source contacts. The TFTs exhibit electron and hole charge carrier mobilities of 30-50 cm{sup 2}/Vs and 10-15 cm{sup 2}/Vs, respectively. In this work, the electrical characteristics of the top-gate ambipolar {mu}c-Si:H TFTs are described by a simple analytical model that takes the ambipolar transport into account. The analytical expressions are used to model the transfer curves, the potential and the net surface charge along the channel of the TFTs. The electrical model provides insights into the electronic transport of ambipolar {mu}c-Si:H TFTs (copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  12. Electrical detection of spin coherence in microcrystalline pin solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Behrends, Jan [Hahn-Meitner-Institut Berlin, Abt. Silizium-Photovoltaik, Berlin (Germany); Department of Physics, University of Utah, Salt Lake City, UT (United States); Boehme, Christoph; Lips, Klaus [Hahn-Meitner-Institut Berlin, Abt. Silizium-Photovoltaik, Berlin (Germany); Haas, Stefan [Institute of Photovoltaics, Forschungszentrum Juelich, Juelich (Germany); Rech, Bernd [Hahn-Meitner-Institut Berlin, Abt. Silizium-Photovoltaik, Berlin (Germany); Institute of Photovoltaics, Forschungszentrum Juelich, Juelich (Germany)

    2007-07-01

    Defects in the band gap of hydrogenated microcrystalline silicon ({mu}cSi:H) pin solar cells, even at low concentrations, can act as recombination centres and thus, they can influence the electronic properties of the device significantly. A powerful technique to investigate these recombination processes is pulsed electrically detected magnetic resonance (pEDMR). This method is based on transient photocurrent measurements after varying specific recombination or transport rates and reveals information about the microscopic mechanisms of recombination and transport that involve paramagnetic states. In this study we report on the application of pEDMR on state-of-the-art {mu}c-Si:H pin solar cells prepared on ZnO coated glass. An adapted contact structure allows the observation of Rabi oscillations in the photocurrent at low temperatures (T=10 K) reflecting coherent spin motion. The coherence time is found to be on the order of several hundred nanoseconds and is determined by recombination. A Fourier analysis of the observed Rabi oscillations allows a distinction between the involved recombination processes. A discussion on the different recombination mechanisms in {mu}c-Si:H cells is given.

  13. Synthesis and characterization of cellulose derivatives obtained from bacterial cellulose; Sintese e caracterizacao de derivados celulosicos obtidos a partir da celulose bacteriana

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Rafael L. de; Barud, Hernane; Ribeiro, Sidney J.L.; Messaddeq, Younes, E-mail: rafael.tu@gmail.com [Instituto de Quimica - Universidade Estadual Paulista Julio de Mesquita Filho - UNESP, Araraquara, SP (Brazil)

    2011-07-01

    The chemical modification of cellulose leads to production of derivatives with different properties from those observed for the original cellulose, for example, increased solubility in more traditional solvents. In this work we synthesized four derivatives of cellulose: microcrystalline cellulose, cellulose acetate, methylcellulose and carboxymethylcellulose using bacterial cellulose as a source. These were characterized in terms of chemical and structural changes by examining the degree of substitution (DS), infrared spectroscopy (FTIR) and nuclear magnetic resonance spectroscopy - NMR {sup 13}C. The molecular weight and degree of polymerization were evaluated by viscometry. The characterization of the morphology of materials and thermal properties were performed with the techniques of X-ray diffraction, electron microscopy images, differential scanning calorimetry (DSC) and thermogravimetric analysis. (author)

  14. Effect of Acid Hydrolysis Conditions on the Properties of Cellulose Nanoparticle-Reinforced Polymethylmethacrylate Composites

    Directory of Open Access Journals (Sweden)

    Guangping Han

    2013-12-01

    Full Text Available Cellulose nanoparticles (CNPs were prepared from microcrystalline cellulose using two concentration levels of sulfuric acid (i.e., 48 wt% and 64 wt% with produced CNPs designated as CNPs-48 and CNPs-64, respectively followed by high-pressure homogenization. CNP-reinforced polymethylmethacrylate (PMMA composite films at various CNP loadings were made using solvent exchange and solution casting methods. The ultraviolet-visible (UV-vis transmittance spectra between 400 and 800 nm showed that CNPs-64/PMMA composites had a significantly higher optical transmittance than that of CNPs-48/PMMA. Their transmittance decreased with increased CNP loadings. The addition of CNPs to the PMMA matrix reduced composite’s coefficient of thermal expansion (CTE, and CNPs-64/PMMA had a lower CTE than CNPs-48/PMMA at the same CNP level. Reinforcement effect was achieved with the addition of CNPs to the PMMA matrix, especially at higher temperature levels. CNPs-64/PMMA exhibited a higher storage modulus compared with CNPs-48/PMMA material. All CNP-reinforced composites showed higher Young’s modulus and tensile strengths than pure PMMA. The effect increased with increased CNP loadings in the PMMA matrix for both CNPs-64/PMMA and CNPs-48/PMMA composites. CNPs affected the Young’s modulus more than they affected the tensile strength.

  15. Role of the components of the cellulase complex on hydrolysis of insoluble cellulose

    Energy Technology Data Exchange (ETDEWEB)

    Klyosov, A.A.; Goldstein, G.C.; Kude, J.; Meyer, D.

    1986-01-01

    The kinetics of the hydrolysis of microcrystalline cellulose (MC) by a Trichoderma reesei cellulase complex and by the individual endoglucanase (pI 4.4-5.2) and cellobiohydrolase (pI 4.0-4.2) has been studied. A flow chart for the enzymatic hydrolysis of the cellulose has been revealed, which formed a basis for a computer simulation of the kinetic regularities observed. As a result of it, the values of the catalytic rate constants for the individual stages of the enzymatic degradation of MC have been calculated. Then, the synergistic behaviour of endoglucanase and cellobiohydrolase in the hydrolysis of MC has been described both quantitatively and graphically. The relative efficiency of the individual stages for the MC hydrolysis in terms of glucose and cellobiose formation for cellulase complexes of various composition has been calculated. It was quantitatively shown that cellobiohydrolase plays the key role in the MC hydrolysis by T. reesei cellulase preparations, because it gives up to 80% glucose and up to 80-90% cellobiose in the presence of endoglucanase which in turn plays a relatively minor role in a direct formation of both soluble products of the hydrolysis.

  16. Ultrasonic dyeing of cellulose nanofibers.

    Science.gov (United States)

    Khatri, Muzamil; Ahmed, Farooq; Jatoi, Abdul Wahab; Mahar, Rasool Bux; Khatri, Zeeshan; Kim, Ick Soo

    2016-07-01

    Textile dyeing assisted by ultrasonic energy has attained a greater interest in recent years. We report ultrasonic dyeing of nanofibers for the very first time. We chose cellulose nanofibers and dyed with two reactive dyes, CI reactive black 5 and CI reactive red 195. The cellulose nanofibers were prepared by electrospinning of cellulose acetate (CA) followed by deacetylation. The FTIR results confirmed complete conversion of CA into cellulose nanofibers. Dyeing parameters optimized were dyeing temperature, dyeing time and dye concentrations for each class of the dye used. Results revealed that the ultrasonic dyeing produced higher color yield (K/S values) than the conventional dyeing. The color fastness test results depicted good dye fixation. SEM analysis evidenced that ultrasonic energy during dyeing do not affect surface morphology of nanofibers. The results conclude successful dyeing of cellulose nanofibers using ultrasonic energy with better color yield and color fastness results than conventional dyeing.

  17. Preparation of multiparticulate systems for oral delivery of a micronized or nanosized poorly soluble drug.

    Science.gov (United States)

    Cerea, Matteo; Pattarino, Franco; Foglio Bonda, Andrea; Palugan, Luca; Segale, Lorena; Vecchio, Carlo

    2016-09-01

    The purpose of the present work was to prepare multiparticulate drug delivery systems for oral administration of a poorly soluble drug such as itraconazole. Multiparticulate systems were prepared by extrusion/spheronization technique using a mix of crospovidone, low viscosity hypromellose, microcrystalline cellulose, micronized drug and water. In order to improve the release performance of the multiparticulate systems, the micronized drug was suspended in water with polysorbate 20 and nanonized by a high-pressure homogenization. The suspension of drug nanoparticles was then spray-dried for enabling an easy handling of the drug and for preventing the over-wetting of the powders during extrusion/spheronization processing. Both multiparticulate units prepared with micronized or nanonized drug showed acceptable disintegrating properties. The nanosizing of micronized drug powder provided a significant improvement of drug dissolution rates of the multiparticulates.

  18. Preparation of well-dispersed gold/magnetite nanoparticles embedded on cellulose nanocrystals for efficient immobilization of papain enzyme.

    Science.gov (United States)

    Mahmoud, Khaled A; Lam, Edmond; Hrapovic, Sabahudin; Luong, John H T

    2013-06-12

    A nanocomposite consisting of magnetite nanoparticles (Fe3O4NPs) and Au nanoparticles (AuNPs) embedded on cellulose nanocrystals (CNCs) was used as a magnetic support for the covalent conjugation of papain and facilitated recovery of this immobilized enzyme. Fe3O4NPs (10-20 nm in diameter) and AuNPs (3-7 nm in diameter) were stable and well-dispersed on the CNC surface. Energy-dispersive spectroscopy, X-ray diffraction, and Fourier transform infrared spectroscopy were used to evaluate the surface composition and structure of CNC/Fe3O4NPs/AuNPs. The nanocomposite was successfully used for the immobilization and separation of papain from the reaction mixture. The optimal enzyme loading was 186 mg protein/g CNC/Fe3O4NPs/AuNPs, significantly higher than the value reported in the literature. The activity of immobilized papain was studied by electrochemical detection of its specific binding to the Thc-Fca-Gly-Gly-Tyr-Arg inhibitory sequence bound to an Au electrode. The immobilized enzyme retained 95% of its initial activity after 35 days of storage at 4 °C, compared to 41% for its free form counterpart.

  19. Influence of the crystalline structure of cellulose on the production of ethanol from lignocellulose biomass

    Science.gov (United States)

    Smuga-Kogut, Małgorzata; Zgórska, Kazimiera; Szymanowska-Powałowska, Daria

    2016-01-01

    In recent years, much attention has been devoted to the possibility of using lignocellulosic biomass for energy. Bioethanol is a promising substitute for conventional fossil fuels and can be produced from straw and wood biomass. Therefore, the aim of this paper was to investigate the effect of 1-ethyl-3-methylimidazolium pretreatment on the structure of cellulose and the acquisition of reducing sugars and bioethanol from cellulosic materials. Material used in the study was rye straw and microcrystalline cellulose subjected to ionic liquid 1-ethyl-3-methylimidazolium pretreatment. The morphology of cellulose fibres in rye straw and microcrystalline cellulose was imaged prior to and after ionic liquid pretreatment. Solutions of ionic liquid-treated and untreated cellulosic materials were subjected to enzymatic hydrolysis in order to obtain reducing sugars, which constituted a substrate for alcoholic fermentation. An influence of the ionic liquid on the cellulose structure, accumulation of reducing sugars in the process of hydrolysis of this material, and an increase in ethanol amount after fermentation was observed. The ionic liquid did not affect cellulolytic enzymes negatively and did not inhibit yeast activity. The amount of reducing sugars and ethyl alcohol was higher in samples purified with 1-ethyl-3-methy-limidazolium acetate. A change in the supramolecular structure of cellulose induced by the ionic liquid was also observed.

  20. Preparation and Characterization of All-Biomass Soy Protein Isolate-Based Films Enhanced by Epoxy Castor Oil Acid Sodium and Hydroxypropyl Cellulose

    Directory of Open Access Journals (Sweden)

    La Wang

    2016-03-01

    Full Text Available All-biomass soy protein-based films were prepared using soy protein isolate (SPI, glycerol, hydroxypropyl cellulose (HPC and epoxy castor oil acid sodium (ECOS. The effect of the incorporated HPC and ECOS on the properties of the SPI film was investigated. The experimental results showed that the tensile strength of the resultant films increased from 2.84 MPa (control to 4.04 MPa and the elongation at break increased by 22.7% when the SPI was modified with 2% HPC and 10% ECOS. The increased tensile strength resulted from the reaction between the ECOS and SPI, which was confirmed by attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR, scanning electron microscopy (SEM and X-ray diffraction analysis (XRD. It was found that ECOS and HPC effectively improved the performance of SPI-based films, which can provide a new method for preparing environmentally-friendly polymer films for a number of commercial applications.

  1. Preparation and characterization of chitosan/cellulose blend films using ZnCl2·3H2O as a solvent

    Directory of Open Access Journals (Sweden)

    Shan Lin

    2012-11-01

    Full Text Available Chitosan (CS/cellulose (BC blend films were successfully prepared using ZnCl2•3H2O as a solvent. Homogeneous structures without obvious phase separation between CS and BC for all blend films were observed by scanning electron microscope (SEM analysis. The tensile strengths of CS/BC blend films decreased with the increase of chitosan content. The results of X-ray diffraction (XRD analysis indicated that the crystal structures of BC and CS were disrupted during the processes of dissolving and regeneration. Also, the reformation of hydrogen bonds between CS and BC during dissolution and regeneration processes resulted in the shift of diffraction peaks. Fourier transforms infrared spectroscopy (FT-IR and thermogravimetric analysis (TGA analysis results confirmed this observation. Moreover, obvious antimicrobial capability of CS/BC blend films against E. coli has been observed, indicating that antibacterial activity of chitosan has not been significantly inactivated while using ZnCl2•3H2O as a solvent. Therefore, ZnCl2•3H2O can be regarded as a promising solvent to prepare degradable films with antibacterial properties.

  2. rf excited optical emission spectrum of radicals generated during hot wire chemical vapour deposition for the preparation of microcrystalline silicon thin film%射频激发热丝化学气相沉积制备硅薄膜过程中光发射谱的研究

    Institute of Scientific and Technical Information of China (English)

    李天微; 刘丰珍; 朱美芳

    2011-01-01

    To study the radicals behavior in the hot wire chemical vapour deposition (HWCVD) process for the preparation of microcrystalline Si (μc-Si: H) thin film, a weak radio frequency (rf) power was introduced to excite the radicals generated in HWCVD chamber. The spectrum of fi-excited HWCVD (rf-HWCVD) was obtained by subtracting the emission of hot wires from the spectrum measured by OES. The influence of the rf power on the rf-HWCVD spectrum can be neglected as the rf power density was less than 0. 1 W/cm2. Under the same deposition parameters, the emission spectra for rf-HWCVD and plasma enhanced CVD (PECVD) processes are different. Under the low deposition pressure ( 7.5 Pa), the intensities of Sill * and Hα vary with the hot wire temperature reversely, which is characteristic of HWCVD with high gas dissociation rate and high concentration of atomic H. The ratio of intensity of Hα to Sill * in the emission spectrum of rf-HWCVD varying with deposition pressure is consistent with the crystalline fraction of μc-Si: H film. The results indicate that the optical emission spectroscopy measurement is a suitable method for the investigation of the HWCVD process excited by a weak rf-power.%采用射频(rf)激发,在热丝化学气相沉积(HWCVD)制备微晶硅薄膜的过程中产生发光基元,测量了rf激发HWCVD(rf-HWCVD)的光发射谱,比较了相同工艺条件下rf-HWCVD和等离子体增强CVD(PECVD)的光发射谱,分析了rf功率、热丝温度和沉积气压对rf-HWCVD光发射谱的影响.结果表明,在射频功率<0.1W/cm1时,rf-HWCVD发射光谱反映了HWCVD高的气体分解效率和高浓度原子氢的特点,能够解释气压变化与微晶硅薄膜微结构的关系,是研究HWCVD气相过程的有效方法之一.

  3. Cellulose is not just cellulose

    DEFF Research Database (Denmark)

    Hidayat, Budi Juliman; Felby, Claus; Johansen, Katja Salomon

    2012-01-01

    or enzymatic hydrolysis of plant cell walls is carried out simultaneously with the application of shear stress, plant cells such as fibers or tracheids break at their dislocations. At present it is not known whether specific carbohydrate binding modules (CBMs) and/or cellulases preferentially access cellulose......Most secondary plant cell walls contain irregular regions known as dislocations or slip planes. Under industrial biorefining conditions dislocations have recently been shown to play a key role during the initial phase of the enzymatic hydrolysis of cellulose in plant cell walls. In this review we...... are not regions where free cellulose ends are more abundant than in the bulk cell wall. In more severe cases cracks between fibrils form at dislocations and it is possible that the increased accessibility that these cracks give is the reason why hydrolysis of cellulose starts at these locations. If acid...

  4. Influence of Cellulose on the Mechanical and Thermal Stability of ABS Plastic Composites

    Directory of Open Access Journals (Sweden)

    K. Crews

    2016-01-01

    Full Text Available Microcrystalline cellulose was explored as possible biodegradable fillers in the fabrication of ABS plastic composites. TGA indicates that upon inclusion of cellulose microcrystals the thermal stability of the ABS plastics was improved significantly when compared to the neat ABS plastic counterparts. Furthermore, inclusion of extracted cellulose from plant biomass showed a higher thermal stability with maximum decomposition temperatures around 131.95°C and 124.19°C for cellulose from cotton and Hibiscus sabdariffa, respectively, when compared to that of the purchased cellulose. In addition, TMA revealed that the average CTE value for the neat ABS and 1 : 1 ratio of cellulose to ABS fabricated in this study was significantly lower than the reported CTE (ca. 73.8 μm/m°C.

  5. Efficient production of glucose by microwave-assisted acid hydrolysis of cellulose hydrogel.

    Science.gov (United States)

    Sun, Binzhe; Duan, Lian; Peng, Gege; Li, Xiaoxia; Xu, Aihua

    2015-09-01

    To improve the production of glucose from cellulose, a simple and effective route was developed. This process uses a combination of a step of cellulose dissolution in aqueous NaOH/urea solution and then regeneration with water, followed by an acid hydrolysis step under microwave irradiation. The method is effective to obtain glucose from α-cellulose, microcrystalline cellulose, filter paper, ramie fiber and absorbent cotton. Increased with the acid concentration the glucose yield from hydrogel hydrolysis increased from 0.42% to 44.6% at 160 °C for 10 min. Moreover, the ozone treatment of cellulose in NaOH/urea solution before regeneration significantly enhanced the hydrolysis efficiency with a glucose yield of 59.1%. It is believed that the chains in cellulose hydrogel are relatively free approached, making that the acids easily access the β-glycosidic bonds. Copyright © 2015 Elsevier Ltd. All rights reserved.

  6. Characteristics of regenerated nanocellulosic fibers from cellulose dissolution in aqueous solutions for wood fiber/polypropylene composites

    Science.gov (United States)

    Sangyeob Lee; Hui Pan; Chung Y. Hse; Alfred R. Gunasekaran; Todd F. Shupe

    2014-01-01

    The effects of aqueous solutions were evaluated on the properties of regenerated cellulosic nanofibers prepared from pure cellulose fibers in various formulations of aqueous solutions. Thermoplastic composites were prepared with reinforcement of the regenerated cellulosic nanofibers. The regenerated cellulosic fibers from cellulosic woody biomass were obtained from...

  7. Preparation of Bacterial Cellulose Nanofiber Through Electrospinning%静电纺丝法制备细菌纤维素纳米纤维

    Institute of Scientific and Technical Information of China (English)

    关晓辉; 于磊; 鲁敏; 张月明

    2013-01-01

    Using bacterial cellulose (BC) as raw material,room temperature ionic liquid AMIMCL as a solution system,the bacterial cellulose nanofibers were prepared through electrospinning technology.Co-solvent N,N-dimethyl formamide (DMF) was added to reduce the viscosity of spinning fluid,and a rotating drum collector was designed and applied.The influences of BC mass fraction,DMF amount,voltage,and curing distance on the spinning process were investigated.The electrospun nanofibers were analyzed by optical microscope,SEM and XRD.The experimental results showed that,when BC mass fraction,ratio of AMIMCL to DMF,voltage,curing distance,and environmental humidity were 5%,1:2.5,23 kV,12 cm,and 60%-80%,respectively,the electrospun B(nanofibers were continuous and the diameter was 500-800 nm.The crystal structure of BC was cellulose of type-Ⅰ,but after BC was dissolved by ionic liquid and electrospun into nanofibers,its crystal structure conversed into cellulose type-Ⅱ.%利用静电纺丝技术,以实验室自制的细菌纤维素(BC)为原材料,选择室温离子液体1-烯丙基-3-甲基咪唑氯化物(AMIMCL)为溶解体系,制备出细菌纤维素纳米纤维.实验中通过添加助溶剂N,N-二甲基甲酰胺(DMF)降低纺丝液的粘度,并设计了转动的滚筒收集器,考察了BC质量分数、DMF的添加量、电压、固化距离等因素对静电纺丝的影响,利用光学显微镜、扫描电子显微镜(SEM)以及X射线衍射(XRD)对纺丝进行分析.研究表明,在BC质量分数为5%、AMIMCL与DMF的质量比为1:2.5、电压为23 kV、固化距离为12 cm、环境湿度为60%~80%的条件下能够制备出连续的、直径为500~800nm的细菌纤维素纳米纤维;BC的晶体结构为纤维素Ⅰ型,而BC经离子液体溶解并静电纺丝后其结构转化为纤维素Ⅱ型.

  8. 纳米纤丝化纤维素制备及硅烷化改性%Preparation and Silanization Modification of Nanofibrillated Cellulose

    Institute of Scientific and Technical Information of China (English)

    王钰; 刘志明

    2015-01-01

    以脱脂棉为原料,高压均质法制备纳米纤丝化纤维素(NFC),并以三甲基氯硅烷和十八烷基三氯硅烷为改性剂,分别对NFC进行硅烷化改性。采用透射电子显微镜( TEM)、傅里叶变换红外光谱( FT-IR)、X射线衍射光谱( XRD)、扫描电子显微镜( SEM)对NFC和硅烷化改性NFC的超微形貌和结构等进行表征。研究结果表明NFC超微形貌呈纤丝状,直径尺寸大多为20 nm,长度尺寸主要分布在500~1000 nm,结构为纤维素Ⅰ型;FT-IR和SEM分析结果表明所制备的硅烷化改性NFC中,150μL三甲基氯硅烷改性NFC的改性效果较好,其超微形貌呈纤丝状。%Nanofibrillated cellulose ( NFC ) was prepared by high pressure homogenization method with absorbent cotton as raw materials. NFCs modified with chlorotrimethylsilane( TMCS) and octadecyltrichlorosilane were prepared respectively. Ultrastructral morphologies and structures of NFC, and silanization modified NFC were characterized by transmission electron microscopy (TEM),fourier transform infrared spectroscopy (FT-IR),X-ray diffraction spectroscopy(XRD),scanning electron microscopy (SEM),respectively. The research results show that the ultrastructral morphology of NFC is fibrillar,and its diameter is mostly about 20 nm,its length is mainly distributed in 500-1 000 nm,and its structure is cellulose type I. The results of FT-IR and SEM analysis show that the modified effect of 150μL TMCS is better than others in the silanization modifications,and the ultrastructral morphology of the accordingly modified NFC is fibrillar.

  9. [Preparation and evaluation of press-coated aminophylline tablet using crystalline cellulose and polyethylene glycol in the outer shell for timed-release dosage forms].

    Science.gov (United States)

    Watanabe, Yoshiteru; Mukai, Baku; Kawamura, Ken-ichi; Ishikawa, Tatsuya; Namiki, Michihiro; Utoguchi, Naoki; Fujii, Makiko

    2002-02-01

    In an attempt to achieve chronopharmacotherapy for asthma, press-coated tablets (250 mg), which contained aminophylline in the core tablet in the form of low-substituted hydroxypropylcellulose (L-HPC) and coated with crystalline cellulose (PH-102) and polyethylene glycol (PEG) at various molecular weights and mixing ratios in the amounts of PH-102 and PEG as the outer shell (press-coating material), were prepared (chronopharmaceutics). Their applicability as timed-release (delayed-release) tablets with a lag time of disintegration and a subsequent rapid drug release phase was investigated. Various types of press-coated tablets were prepared using a tableting machine, and their aminophylline dissolution profiles were evaluated by the JP paddle method. Tablets with the timed-release characteristics could be prepared, and the lag time of disintegration was prolonged as the molecular weight and the amount of PEG, for example PEG 500,000, in the outer shell were increased. The lag time of disintegration could be controlled by the above-mentioned method, however, the pH of the medium had no effect on disintegration of the tablet and dissolution behavior of theophylline. The press-coated tablet (core tablet:aminophylline 50 mg, L-HPC and PEG 6000; outer shell:PH-102:PEG = 8:2 200 mg) with the timed-release characteristics was administered orally to rabbits for an in vivo test. Theophylline was first detected in plasma more than 2 h after administration; thus, this tablet showed a timed-release characteristics in the gastrointestinal tract. The time (tmax) required to reach the maximum plasma theophylline concentration (Cmax) observed after administration of the press-coated tablet was significantly (p 24) between the press-coated tablet and aminophylline solution. These results suggest that the press-coated aminophylline tablet (with the timed-release characteristic) offers a promising forms of theophylline chronotherapy for asthma.

  10. Preparation of poly(3-hydroxybutyrate)/carboxymethyl cellulose acetate butyrate blends using gel formation;Preparacao de blendas de poli(3-hidroxibutirato)/acetato butirato de carboximetilcelulose por gelificacao

    Energy Technology Data Exchange (ETDEWEB)

    Gomes, A.L.; Rodrigues, G.V.; Goncalves, M.C., E-mail: agomes@iqm.unicamp.b [Universidade Estadual de Campinas (IQ/UNICAMP), SP (Brazil). Inst. de Quimica

    2009-07-01

    This study investigates poly(3-hydroxybutyrate) (PHB) gel formation with a binary combination of solvents and its use on the preparation of PHB and carboxymethyl cellulose acetate butyrate (CMCAB) blends. The gel preparation method was compared to a precipitation method followed by hot pressing. The results from DSC and X-ray diffractions showed that both methodologies produced blends with very similar thermal properties and crystallization behavior. Scanning electron microscopy indicated better homogeneity in gel formation blends. Apart from this, the gel formation methodology provided new ways to prepare immiscible blends with the advantage of using friendlier solvents. (author)

  11. Sensing the structural differences in cellulose from apple and bacterial cell wall materials by Raman and FT-IR spectroscopy.

    Science.gov (United States)

    Szymańska-Chargot, Monika; Cybulska, Justyna; Zdunek, Artur

    2011-01-01

    Raman and Fourier Transform Infrared (FT-IR) spectroscopy was used for assessment of structural differences of celluloses of various origins. Investigated celluloses were: bacterial celluloses cultured in presence of pectin and/or xyloglucan, as well as commercial celluloses and cellulose extracted from apple parenchyma. FT-IR spectra were used to estimate of the I(β) content, whereas Raman spectra were used to evaluate the degree of crystallinity of the cellulose. The crystallinity index (X(C)(RAMAN)%) varied from -25% for apple cellulose to 53% for microcrystalline commercial cellulose. Considering bacterial cellulose, addition of xyloglucan has an impact on the percentage content of cellulose I(β). However, addition of only xyloglucan or only pectins to pure bacterial cellulose both resulted in a slight decrease of crystallinity. However, culturing bacterial cellulose in the presence of mixtures of xyloglucan and pectins results in an increase of crystallinity. The results confirmed that the higher degree of crystallinity, the broader the peak around 913 cm(-1). Among all bacterial celluloses the bacterial cellulose cultured in presence of xyloglucan and pectin (BCPX) has the most similar structure to those observed in natural primary cell walls.

  12. Sensing the Structural Differences in Cellulose from Apple and Bacterial Cell Wall Materials by Raman and FT-IR Spectroscopy

    Directory of Open Access Journals (Sweden)

    Artur Zdunek

    2011-05-01

    Full Text Available Raman and Fourier Transform Infrared (FT-IR spectroscopy was used for assessment of structural differences of celluloses of various origins. Investigated celluloses were: bacterial celluloses cultured in presence of pectin and/or xyloglucan, as well as commercial celluloses and cellulose extracted from apple parenchyma. FT-IR spectra were used to estimate of the Iβ content, whereas Raman spectra were used to evaluate the degree of crystallinity of the cellulose. The crystallinity index (XCRAMAN% varied from −25% for apple cellulose to 53% for microcrystalline commercial cellulose. Considering bacterial cellulose, addition of xyloglucan has an impact on the percentage content of cellulose Iβ. However, addition of only xyloglucan or only pectins to pure bacterial cellulose both resulted in a slight decrease of crystallinity. However, culturing bacterial cellulose in the presence of mixtures of xyloglucan and pectins results in an increase of crystallinity. The results confirmed that the higher degree of crystallinity, the broader the peak around 913 cm−1. Among all bacterial celluloses the bacterial cellulose cultured in presence of xyloglucan and pectin (BCPX has the most similar structure to those observed in natural primary cell walls.

  13. Investigation into the suitability of capillary tubes for microcrystalline testing.

    Science.gov (United States)

    Elie, Leonie E; Baron, Mark G; Croxton, Ruth S; Elie, Mathieu P

    2013-07-01

    A comparison between microcrystalline tests performed on microscope slides and flat capillary tubes with inner diameters ranging from 0.1 to 0.7 mm was carried out to explore the appropriateness of tubes for rapid testing of suspected drugs of abuse in the laboratory as well as in the field. Tests for mephedrone, cocaine, and phencyclidine were chosen as examples to investigate the handling of the capillary tubes, the influence on crystal habit, size, and the effects on the limit of detection. Image stacking software was used to increase the depth of field of micrographs taken from developed microcrystals greatly enhancing the interpretability even months after carrying out the microcrystalline test. Additionally, the potential of seeding capillary tubes with a reagent was studied. Pre-treatment of tubes would allow microcrystalline tests to be carried out quicker and anywhere without the necessity of taking along expensive and hazardous reagents. The sealing of capillary tubes containing developed microcrystalline tests in order to preserve results for a long period of time was successfully done by applying paraffin wax to the open ends. Finally, it was concluded that capillary tubes are suitable vessels for performing microcrystalline tests. The increased portability of the improved set-up allows tests to be safely executed outside laboratories without impairing the quality of the result. Findings were applied to six legal high samples purchased online between May and August 2011. The active ingredients like MDAI as well as cutting agents like caffeine were successfully identified using the microcrystalline test technique in capillary tubes.

  14. 基于溶胶-凝胶技术制备纳米纤维素的表征%Characterization of Nano-cellulose with Sol-gel Method

    Institute of Scientific and Technical Information of China (English)

    谢成; 刘志明; 王海英; 孟围

    2012-01-01

    通过傅里叶变换红外光谱、X射线衍射、热重、透射电子显微镜分析及激光粒度分析对基于溶胶-凝胶技术制备的纳米纤维素进行表征,结果表明原料微晶纤维素超分子结构为纤维素Ⅰ型,制备的纳米纤维素为纤维素Ⅱ型;微晶纤维素的结晶度为87.54%,纳米纤维素的结晶度为73.49%,纳米纤维素结晶度较微晶纤维素有所下降;制备的纳米纤维素热稳定性低于微晶纤维素;纳米纤维素平均粒度425 nm,粒度分布呈现正态分布;纳米纤维素长径比为5∶1~40∶1。%Nano-cellulose prepared by sol-gel method was characterized by using Fourier transform infrared(FTIR) spectroscopy,X-ray diffraction(XRD),thermal gravimetric analysis(TGA),transmission electron microscopy(TEM) and laser particle size test.The results showed that supramolecular structure of microcrystalline cellulose(MCC) as raw material was cellulose I,while the prepared nano-cellulose was cellulose Ⅱ.The crystallinity of MCC was calculated as 87.54 %,for nano-cellulose,the crystallinity was 73.49 %.The crystallinity of nano-cellulose decreased slightly compared with that of MCC.The thermal stability of nano-cellulose was less than that of MCC.The mean size of nano-cellulose was 425 nm,its particle size distribution appeared normal distribution.Aspect ratio of nano-cellulose was 5∶1 to 40∶1.

  15. Preparation of Mg(OH)2 hybrid pigment by direct precipitation and graft onto cellulose fiber via surface-initiated atom transfer radical polymerization

    Science.gov (United States)

    Wang, Xiao; Zhang, Yue; Lv, Lihua; Cui, Yongzhu; Wei, Chunyan; Pang, Guibing

    2016-02-01

    Mg(OH)2 flame retardant hybrid pigment is synthesized through simultaneous solution precipitation and adsorption of anionic dyes (C.I. Acid Red 6). The Mg(OH)2 hybrid pigment bearing vinyl groups after surface silane modification is immobilized onto the surface of bromo end-functional cellulose fiber by atom transfer radical polymerization (ATRP). The morphology and structure of Mg(OH)2 pigments and cellulose fibers grafted with modified pigments are characterized. The thermal properties, flammability and color fastness of cellulose fibers grafted with modified pigments are measured. The results reveal that anionic dye molecules are adsorbed onto Mg(OH)2 crystals and affect the formation of lamella-like Mg(OH)2 crystals. The cellulose fiber grafted with modified Mg(OH)2 hybrid pigment absorbs about four times heat more than original cellulose fiber with about 4% immobilization ratio of pigment, which shortens nearly half of afterflame time and afterglow time.

  16. Comparison of physical properties of regenerated cellulose films fabricated with different cellulose feedstocks in ionic liquid.

    Science.gov (United States)

    Pang, JinHui; Wu, Miao; Zhang, QiaoHui; Tan, Xin; Xu, Feng; Zhang, XueMing; Sun, RunCang

    2015-05-05

    With the serious "white pollution" resulted from the non-biodegradable plastic films, considerable attention has been directed toward the development of renewable and biodegradable cellulose-based film materials as substitutes of petroleum-derived materials. In this study, environmentally friendly cellulose films were successfully prepared using different celluloses (pine, cotton, bamboo, MCC) as raw materials and ionic liquid 1-ethyl-3-methylimidazolium acetate as a solvent. The SEM and AFM indicated that all cellulose films displayed a homogeneous and smooth surface. In addition, the FT-IR and XRD analysis showed the transition from cellulose I to II was occurred after the dissolution and regeneration process. Furthermore, the cellulose films prepared by cotton linters and pine possessed the most excellent thermal stability and mechanical properties, which were suggested by the highest onset temperature (285°C) and tensile stress (120 MPa), respectively. Their excellent properties of regenerated cellulose films are promising for applications in food packaging and medical materials.

  17. PRODUCTION AND CHARACTERIZATION OF ECONOMICAL BACTERIAL CELLULOSE

    Directory of Open Access Journals (Sweden)

    Houssni El-Saied

    2008-11-01

    Full Text Available The present study investigates the economical production of bacterial cellulose (BC by Gluconacetobacter subsp. Xylinus (ATCC 10245 in 250 ml Erlenmeyer flasks cultivated under static conditions. The fermentation media used contained food industrial by-product liquors, such as black strap molasses solution and corn steep liquor (CSL, which represents some of the most economical carbon and nitrogen sources. However, because of the presence of undesirable components in molasses (such as coloring substances, heavy metals, and other compounds that may act as inhibitors, and in order to eliminate them, crude molasses has been treated with an acid, as an attempt to increase BC productivity. The amount of BC produced using these carbon and nitrogen sources was determined and compared to that produced using previously reported fermentation media. The characterizations of the bacterial cellulose (BC pellicles obtained using either conventional or by-product media were studied by thermal and spectral techniques and compared to those of plant-derived cellulose such as cotton linter, viscose pulp, and microcrystalline cellulose.

  18. Fabrication and characterization of novel biomimetic PLLA/cellulose/hydroxyapatite nanocomposite for bone repair applications

    Energy Technology Data Exchange (ETDEWEB)

    Eftekhari, Samin [Department of Chemical Engineering, Ryerson University, 350 Victoria Street, Toronto, ON M5B 2K3 (Canada); El Sawi, Ihab; Bagheri, Zahra Shaghayegh [Department of Mechanical and Industrial Engineering, Ryerson University, 350 Victoria Street, Toronto, ON M5B 2K3 (Canada); Turcotte, Ginette [Department of Chemical Engineering, Ryerson University, 350 Victoria Street, Toronto, ON M5B 2K3 (Canada); Bougherara, Habiba, E-mail: habiba.bougherara@ryerson.ca [Department of Mechanical and Industrial Engineering, Ryerson University, 350 Victoria Street, Toronto, ON M5B 2K3 (Canada)

    2014-06-01

    The purpose of this research is to develop and characterize a novel biomimetic nanocomposite that closely mimics the properties of real bone such as morphology, composition and mechanical characteristics. This novel porous nanocomposite is composed of cotton-sourced cellulose microcrystals, hydroxyapatite nanoparticles and poly L-lactide acid. A unique combination of commonly used fabrication procedures has been developed including pre-treatment of particles using a coupling agent. The effect of various weight ratios of the reinforcing agents was evaluated to assess their influence on the chemical, thermal, and mechanical properties of the nanocomposites. The prepared nanocomposites were characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, differential scanning calorimetry and compression testing. Our results indicated the presence of molecular interactions between all components leading to an increase of the crystallinity of the polymer from 50% to 80%. Compression test results revealed that increasing the weight ratio of microcrystalline cellulose/poly L-lactide acid and hydroxyapatite/poly L-lactide acid from 0.1 to 0.5 enhanced the compressive yield stress from 0.127 to 2.2 MPa and The Young's modulus from 6.6 to 38 MPa, respectively. It was found that the fabricated nanocomposites are comparable with the trabecular bone from compositional, structural, and mechanical point of view. - Highlights: • Fabrication of PLLA/HA/cellulose composites that mimic the spongeous bone • Homogenous dispersion of the reinforcing agents in the PLLA matrix was attained. • More efficient interface between the PLLA and the reinforcing agents was achieved. • Preliminary in vitro biocompatibility test showed the nontoxicity of the composite. • The crystallinity, the compressive strength and modulus were investigated.

  19. 多孔性再生纤维素磁性微球的制备及性质%Preparation and properties analysis of porous magnetic microspheres from regenerated cellulose

    Institute of Scientific and Technical Information of China (English)

    谷军; 吴伟兵; 王飞; 龚木荣; 景宜; 戴红旗

    2012-01-01

    利用绿色环保的碱-尿素-水溶剂体系制备纤维素溶液,采用反相悬浮法制备纤维素微球,并通过原位复合法工艺对纤维素微球进行纳米磁性功能化负载.结果表明,随着油水比不断增大,微球粒径逐渐减小,制备的再生纤维素微球比表面积超过30m2/g,孔度超过90%,吸水性强,含水率超过85%.通过FTIR、XRD和SEM研究发现原位复合法可成功地生成Fe304纳米粒子,并在纤维素微球中形成有效负载,且制备的纤维复合微球保留了良好的球形结构和多孔性,并具有超顺磁性.%The natural cellulose now has become one of the research hotspats in the water treatment research field for its excellent performance. Natural cellulose was directly dissolved in environmental-friendly alkali/carbamide/water solvent system. Reversed-phase suspension technique was used to regenerate cellulose microspheres, they were further magnetically functionalized through in-situ synthesis method. The results showed that there was a decrease in the diameters of the cellulose microspheres with an increase of the oil/water ratio. The prepared cellulose microspheres had large specific surface area ( >30 mVg) , good porosity ( >90 % ) , and high water content ( > 85 % ). Based on the results of FTIR, XRD and SEM, Fe3O4 nanoparticles were successfully formed and loaded in the cellulose microspheree. The cellulose composites preserved good orbicular shape, porosity and superparamagnetism. This type of cellulose microspheres material possessed potential application in the water treatment field.

  20. Outline of Preparation and Fire- retardant Properties Detection of Nanocrystalline Cellulose Fire- retardant Membranes%纳米纤维素阻燃膜的制备及阻燃性检测概述

    Institute of Scientific and Technical Information of China (English)

    徐睿; 王海英; 孙睿; 雷舒

    2012-01-01

    Methods of fire -retardant properties evaluation, fire -retardant cellulose fibers preparation, and nano- crystalline cellulose preparation were introduced, respectively. The national standards of fire - retardant properties evalua- tion for fire - retardant protective clothing and forest fire - proof clothing were compared. National standards GB/T5454 - 1997, textiles - burning properties test oxygen index method, was used in forest fire - proof clothing. Preparation method and application prospects of nanocrystalline cellulose fire - retardant membranes were explored.%分别介绍了阻燃性能指标评价、阻燃纤维素纤维的制备、纳米纤维素的制备等方法,比较了阻燃防护服和森林防火服的阻燃性能指标评价国家标准,森林防火服的阻燃性能指标评价还另外采用了GB/T5454—1997纺织品燃烧性能试验氧指数法国家标准,探讨了纳米纤维素复合阻燃膜的制备方法及其应用前景。

  1. Enhanced cellulose degradation using cellulase-nanosphere complexes.

    Directory of Open Access Journals (Sweden)

    Craig Blanchette

    Full Text Available Enzyme catalyzed conversion of plant biomass to sugars is an inherently inefficient process, and one of the major factors limiting economical biofuel production. This is due to the physical barrier presented by polymers in plant cell walls, including semi-crystalline cellulose, to soluble enzyme accessibility. In contrast to the enzymes currently used in industry, bacterial cellulosomes organize cellulases and other proteins in a scaffold structure, and are highly efficient in degrading cellulose. To mimic this clustered assembly of enzymes, we conjugated cellulase obtained from Trichoderma viride to polystyrene nanospheres (cellulase:NS and tested the hydrolytic activity of this complex on cellulose substrates from purified and natural sources. Cellulase:NS and free cellulase were equally active on soluble carboxymethyl cellulose (CMC; however, the complexed enzyme displayed a higher affinity in its action on microcrystalline cellulose. Similarly, we found that the cellulase:NS complex was more efficient in degrading natural cellulose structures in the thickened walls of cultured wood cells. These results suggest that nanoparticle-bound enzymes can improve catalytic efficiency on physically intractable substrates. We discuss the potential for further enhancement of cellulose degradation by physically clustering combinations of different glycosyl hydrolase enzymes, and applications for using cellulase:NS complexes in biofuel production.

  2. Preparation and in vitro release performance of sustained-release captopril/Chitosan-gelatin net-polymer microspheres

    Science.gov (United States)

    Zhou, Li; Xu, Junming; Song, Yimin; Gao, Yuanyuan; Chen, Xiguang

    2007-07-01

    The captopril/Chitosan-gelatin net-polymer microspheres (CTP/CGNPMs) were prepared using Chitosan (CTS) and gelatin (GT) by the methods of emulsification, cross-linked reagent alone or in combination and microcrystalline cellulose (MCC) added in the process of preparation of microspheres, which aimed to eliminate dose dumping and burst phenomenon of microspheres for the improvement of the therapeutic efficiency and the decrease of the side effects of captopril (CTP). The results indicated that CTP/CGNPMs had a spherical shape, smooth surface and integral structure inside but no adhesive phenomena in the preparation. The size distribution ranged from 220 μm to 280 μm. The CTP release test in vitro demonstrated that CTP/CGNPMs played the role of retarding the release of CTP compared with ordinary CTP tablets. The release behaviors of CGNPMS were influenced by preparation conditions such as experimental material ratio (EMR) and composition of cross linking reagents. Among these factors, the EMR (1/4), CLR (FA+SPP) and 0.75% microcrystalline cellulose (MCC) added to the microspheres constituted the optimal scheme for the preparation of CTP/CGNPMs. The ER, DL and SR of CTP/CGNPMs prepared according to the optimal scheme were 46.23±4.51%, 9.95±0.77% and 261±42%, respectively. The CTP/CGNPMs had the good characteristics of sustained release of drug and the process of emulsification and cross-linking were simple and stable. The CGNPMs are likely to be an ideal sustained release formulation for water-soluble drugs.

  3. Preparation and in vitro Release Performance of Sustained-release Captopril/Chitosan-gelatin Net-polymer Microspheres

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The captopril/Chitosan-gelatin net-polymer microspheres (CTP/CGNPMs) were prepared using Chitosan (CTS) and gelatin (GT) by the methods of emulsification, cross-linked reagent alone or in combination and microcrystalline cellulose (MCC) added in the process of preparation of microspheres, which aimed to eliminate dose dumping and burst phenomenon of microspheres for the improvement of the therapeutic efficiency and the decrease of the side effects of captopril (CTP). The results indicated that CTP/CGNPMs had a spherical shape, smooth surface and integral structure inside but no adhesive phenomena in the preparation. The size distribution ranged from 220 μm to 280 μm. The CTP release test in vitro demonstrated that CTP/CGNPMs played the role of retarding the release of CTP compared with ordinary CTP tablets. The release behaviors of CGNPMS were influenced by preparation conditions such as experimental material ratio (EMR) and composition of cross linking reagents. Among these factors, the EMR (1/4), CLR (FA+SPP) and 0.75% microcrystalline cellulose (MCC) added to the microspheres constituted the optimal scheme for the preparation of CTP/CGNPMs. The ER, DL and SR of CTP/CGNPMs prepared according to the optimal scheme were 46.23±4.51%, 9.95±0.77% and 261±42%, respectively. The CTP/CGNPMs had the good characteristics of sustained release of drug and the process of emulsification and cross-linking were simple and stable. The CGNPMs are likely to be an ideal sustained release formulation for water-soluble drugs.

  4. Preparation and characterization of nanocrystalline cellulose/silver nanoparticles%纳米纤维素/银纳米粒子的制备和表征

    Institute of Scientific and Technical Information of China (English)

    王海英; 孟围; 刘志明

    2013-01-01

    以纳米纤维素(NCC)为分散剂,硼氢化钠为还原剂还原硝酸银,化学还原法制备纳米纤维素/银纳米粒子.m(Ag)/m (NCC)=5%制备的纳米纤维素/银纳米粒子,X射线衍射分析结果表明,纳米纤维素/银纳米粒子中NCC和银纳米粒子相互混合并未改变各自的晶型,纳米纤维素/银纳米粒子中银纳米粒子的晶粒尺寸为11.87nm,与透射电子显微镜(TEM)所测银纳米粒子直径(10nm)相近;热重分析结果表明,纳米纤维素/银纳米粒子的热稳定性较纳米纤维素稍有下降.透射电子显微镜(TEM)分析、紫外光谱分析、固含量分析、机理分析和抑菌活性分析结果表明,m(Ag)/m (NCC)=3%时制备的纳米纤维素/银纳米粒子对大肠杆菌和金黄色葡萄球菌均有抑制作用,且银纳米粒子在纳米纤维素/银纳米粒子中分散较均匀.%Nanocrystalline cellulose/silver nanoparticles was prepared by chemical reduction method with nanocrystalline cellulose(NCC) as dispersing agent, sodium borohydride as reductant of silver nitrate. For NCC/silver nanoparticles prepared with 5wt% of m (Ag)/m (NCC), X-ray diffraction analysis showed that crystalline type of NCC and silver nanoparticles for NCC/silver nanoparticles did not change respectively. Grain size of silver nanoparticles of NCC/silver nanoparticles was 11. 87nm,which was similar to silver nanoparticles diameter (10nm) measured by transmission electron microscopy (TEM). Thermogravimetric analysis (TGA) results showed that thermal stability of NCC/silver nanoparticles decreased slightly compared with NCC. Transmission electron microscopy (TEM) analysis, UV-Vis absorption spectra analysis, solid content analysis, mechanism a-nalysis, and antibacterial activity analysis results showed that escherichia coli and staphylococcus aureus was separately inhibited by NCC/silver nanoparticles prepared with 3% of m (Ag)/m (NCC) and silver nanoparticles of NCC/silver nanoparticles were uniformly

  5. Observation of a microcrystalline gel in colloids with competing interactions

    NARCIS (Netherlands)

    Zhang, T.; Groenewold, J.; Kegel, W.K.

    2009-01-01

    A stable short-range crystalline structure is observed in colloidal systems with competing short-range attractions and long-range repulsions. We term these structures ‘‘microcrystalline gels’’ as the microcrystals are embedded in a dense disordered network.

  6. Microcrystalline silicon films and solar cells investigatet by photoluminescence spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Merdzhanova, T.

    2005-07-01

    A systematic investigation on photoluminescence (PL) properties of microcrystalline silicon ({mu}c-Si:H) films with structural composition changing from highly crystalline to predominantly amorphous is presented. The samples were prepared by PECVD and HWCVD with different silane concentration in hydrogen (SC). By using photoluminescence in combination with Raman spectroscopy the relationship between electronic properties and the microstructure of the material is studied. The PL spectra of {mu}c-Si:H reveal a rather broad ({proportional_to}0.13 eV) featureless band at about 1 eV ('{mu}c'-Si-band). In mixed phase material of crystalline and amorphous regions, a band at about 1.3 eV with halfwidth of about 0.3 eV is found in addition to '{mu}c'-Si-band, which is attributed to the amorphous phase ('a'-Si-band). Similarly to amorphous silicon, the '{mu}c'-Si-band is assigned to recombination between electrons and holes in band tail states. An additional PL band centred at about 0.7 eV with halfwidth slightly broader than the '{mu}c'-Si-band is observed only for films prepared at high substrate temperature and it is preliminarily assigned to defect-related transitions as in polycrystalline silicon. With decreasing crystalline volume fraction, the '{mu}c'-Si-band shifts continuously to higher energies for all {mu}c-Si:H films but the linewidth of the PL spectra is almost unaffected. This is valid for all deposition conditions investigated. The results are interpreted, assuming decrease of the density of band tail states with decreasing crystalline volume fraction. A simple model is proposed to simulate PL spectra and V{sub oc} in {mu}c-Si:H solar cells as a function of temperature, based on carrier distributions in quasi-equilibrium conditions. In the model is assumed symmetric density of states distributions for electrons and holes in the conduction and the valence band tail states. The best agreement between

  7. Characterization of Type-II Acetylated Cellulose Nanocrystals with Various Degree of Substitution and Its Compatibility in PLA Films

    Directory of Open Access Journals (Sweden)

    Feng Dong

    2017-08-01

    Full Text Available In order to decrease the self-agglomeration and improve the hydrophobic properties of type-II acetylated cellulose nanocrystals (ACNC II, various degree of substitution (DS values of ACNCs were successfully prepared by a single-step method from microcrystalline cellulose with anhydrous phosphoric acid as the solvent, and acetic anhydride as the acetylation reagent, under different reaction temperatures (20–40 °C. To thoroughly investigate the DS values of ACNC II, analyses were performed using Fourier transform infrared spectroscopy (FT-IR, 13C cross polarization-magic angle spinning (CP-MAS nuclear magnetic resonance (NMR, and X-ray photoelectron spectroscopy (XPS. At a reaction temperature of 40°C, the highest DS value was successfully obtained. XRD proved that the crystal structure of ACNC II with various DS values was maintained after acetylation. TEM showed the threadlike shape for ACNC II with various DS values. The ACNC II with various DS values was introduced into a polylactic acid (PLA matrix to produce PLA/ACNC composite films, which showed improved rheological and thermal properties. This improvement was primarily attributed to good dispersion of the ACNC II, and the interfacial compatibility between ACNC II and the PLA matrix. This study aims to analyze the compatibility of ACNC II with various DS values in the PLA matrix by microstructure, crystallization, and rheological and thermal tests.

  8. Preparation and properties of cellulose triacetate forward osmosis membrane%三乙酸纤维素正渗透膜的制备与性能

    Institute of Scientific and Technical Information of China (English)

    解利昕; 辛婧; 解奥

    2014-01-01

    Cellulose triacetate based membranes for forward osmosis were prepared by immersion precipitation. The polymer solution consisted of cellulose triacetate as the membrane material, 1,4-dioxane and acetone as solvent,methanol and lactic acid as additives. Casting composition and preparation conditions-1,4-dioxane/acetone ratio,lactic acid content,evaporation time,casting thickness and annealing temperature-were tested for their effects on membrane performance. The optimized membrane showed 14.10L/(m2·h) water flux and 0.031mol/(m2·h) reverse solute flux using a feed solution of pure water and draw solution of 0.56mol/L CaCl2. When 0.1mol/L NaCl was used as the feed solution and 4mol/L glucose was used as the draw solution,water flux was above 5L/(m2·h) and rejection for NaCl was above 99%. The optimized membrane had a more hydrophilic surface, higher water flux,higher salt resistance and better membrane performance than the HTI membrane.%以三乙酸纤维素(CTA)为膜材料,1,4-二氧六环、丙酮为溶剂,甲醇、乳酸为添加剂,采用相转换法制备了三乙酸纤维素正渗透膜。研究了不同1,4-二氧六环/丙酮配比、添加剂乳酸含量、挥发时间、膜厚度、热处理温度条件下正渗透膜性能的变化规律。研究表明,当采用纯水为原料液,0.56mol/L CaCl2为汲取液时,优化制备的CTA正渗透膜的水通量达到14.10L/(m2·h),溶质反扩散量为0.031mol/(m2·h);采用0.1mol/L NaCl为原料液,4mol/L葡萄糖为汲取液时,优化制备的CTA正渗透膜的水通量保持在5L/(m2·h)以上,对NaCl的截留率大于99%。CTA正渗透膜相比于HTI膜,具有较高的亲水性、水通量、截留率,稳定性更好。

  9. Preparation of Mg(OH){sub 2} hybrid pigment by direct precipitation and graft onto cellulose fiber via surface-initiated atom transfer radical polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xiao, E-mail: wangxiao@dlpu.edu.cn [School of Textile and Materials Engineering, Dalian Polytechnic University, Dalian, Liaoning Province (China); Zhang, Yue; Lv, Lihua; Cui, Yongzhu; Wei, Chunyan [School of Textile and Materials Engineering, Dalian Polytechnic University, Dalian, Liaoning Province (China); Pang, Guibing [School of Mechanical Engineering and Automation, Dalian Polytechnic University, Dalian, Liaoning Province (China)

    2016-02-15

    Graphical abstract: - Highlights: • Adsorbed anionic dye molecules are conducive to preferential growth of (0 0 1) plane of Mg(OH){sub 2} crystal for Mg(OH){sub 2} pigments. • Uniform coverage of nanosized Mg(OH){sub 2} pigments on fiber surface is achieved via surface-initiated ATRP. • About 4 wt% of Mg(OH){sub 2} pigment on fiber surface shortens nearly half of burning time of cellulose. - Abstract: Mg(OH){sub 2} flame retardant hybrid pigment is synthesized through simultaneous solution precipitation and adsorption of anionic dyes (C.I. Acid Red 6). The Mg(OH){sub 2} hybrid pigment bearing vinyl groups after surface silane modification is immobilized onto the surface of bromo end-functional cellulose fiber by atom transfer radical polymerization (ATRP). The morphology and structure of Mg(OH){sub 2} pigments and cellulose fibers grafted with modified pigments are characterized. The thermal properties, flammability and color fastness of cellulose fibers grafted with modified pigments are measured. The results reveal that anionic dye molecules are adsorbed onto Mg(OH){sub 2} crystals and affect the formation of lamella-like Mg(OH){sub 2} crystals. The cellulose fiber grafted with modified Mg(OH){sub 2} hybrid pigment absorbs about four times heat more than original cellulose fiber with about 4% immobilization ratio of pigment, which shortens nearly half of afterflame time and afterglow time.

  10. Preparation and characterization of gatifloxacin-loaded sodium alginate hydrogel membranes supplemented with hydroxypropyl methylcellulose and hydroxypropyl cellulose polymers for wound dressing

    Science.gov (United States)

    Prabu, Durai; Majdalawieh, Amin F.; Abu-Yousef, Imad A.; Inbasekaran, Kadambari; Balasubramaniam, Tharani; Nallaperumal, Narayanan; Gunasekar, Conjeevaram J.

    2016-01-01

    Introduction: The aim of this study is to evaluate gatifloxacin-loaded sodium alginate hydrogel membranes, supplemented with glycerol (a plasticizer), glutaraldehyde (a cross-linking agent), and hydroxypropyl methylcellulose (HPMC) or hydroxypropyl cellulose (HPC) polymers, as potential wound dressing materials based on their physicochemical properties and the sustain-release phenomenon. Materials and Methods: The physicochemical properties of the prepared hydrogel membranes were evaluated by several methods including Fourier transform infrared and differential scanning calorimetry. Different techniques were used to assess the swelling behavior, tensile strength and elongation, % moisture absorption, % moisture loss, water vapor transmission rate (WVTR), and microbial penetration for the hydrogel membranes. In vitro gatifloxacin release from the hydrogel membranes was examined using the United States Pharmacopeia XXIII dissolution apparatus. Four kinetics models (zero-order, first-order, Higuchi equation, and Korsmeyer-Peppas equation) were applied to study drug release kinetics. Results: The addition of glycerol, glutaraldehyde, HPMC, and HPC polymers resulted in a considerable increase in the tensile strength and flexibility/elasticity of the hydrogel membranes. WVTR results suggest that hydrated hydrogel membranes can facilitate water vapor transfer. None of the hydrogel membranes supported microbial growth. HPMC-treated and HPC-treated hydrogel membranes allow slow, but sustained, release of gatifloxacin for 48 h. Drug release kinetics revealed that both diffusion and dissolution play an important role in gatifloxacin release. Conclusions: Given their physicochemical properties and gatifloxacin release pattern, HPMC-treated and HPC-treated hydrogel membranes exhibit effective and sustained drug release. Furthermore, HPMC-treated and HPC-treated hydrogel membranes possess physiochemical properties that make them effective and safe wound dressing materials. PMID

  11. Preparation and Per1formance of Cellulose Nanoparticles-Reinforced Polymethylmethacrylate Composites%纤维素纳米粒子增强聚甲基丙烯酸甲酯复合材料的制备和性能1)

    Institute of Scientific and Technical Information of China (English)

    蔡琪; 韩广萍; 宦思琪; 商璐; 程万里

    2014-01-01

    Cellulose nanoparticles ( CNP) were prepared from microcrystalline cellulose with two content levels of sulfuric acid (48%and 64%) by high-pressure homogenization.The produced CNP was designated as CNP-48 and CNP-64, respec-tively.CNP-reinforced polymethylmethacrylate ( PMMA) composite films at various CNP loadings were fabricated using solvent exchange and solution casting methods.By morphology analysis, CNP/PMMA-64 composites have a significantly higher optical transparency when CNP loading is as high as 20%.By Fourier transform infrared spectroscopy , CNP and PMMA are composited well.By wide angle X-ray diffraction, crystallization index of CNP/PMMA-48-15 and CNP/PMMA-48-20 increase to 20.8%and 26.8%, respectively.Therefore, there is significant reinforcement from CNP.Form differ-ential scanning calorimetry data, by adding CNP to PMMA, the glass transition temperatures of CNP/PMMA-48-20 and CNP/PMMA-64-20 increase by 10℃and 20℃, respectively.The thermal stability of CNP-reinforced composite materials can be highly improved.%以微晶纤维素为原料,通过质量分数为48%和64%的两种硫酸进行化学预处理,经高压均质制备纤维素纳米粒子CNP-48和CNP-64,并以这两种纳米粒子为增强材料采用溶剂置换和溶液重铸法制备 CNP/聚甲基丙烯酸甲酯( PMMA)复合材料。宏观形貌分析结果表明,即使CNP-64的添加量为20%,CNP/PMMA-64-20薄膜材料也表现出良好的光学透光性。傅立叶变换红外光谱数据表明,PMMA与CNP复合良好。广角X射线衍射数据表明,随着CNP添加量的增加,复合材料的结晶度提高,CNP/PMMA-48-15和CNP/PMMA-48-20的结晶度分别增加到20.8%和26.8%,具有显著的增强效果。差示扫描量热数据表明,在PMMA中加入CNP,使CNP/PMMA-48-20和CNP/PMMA-64-20复合材料的玻璃化转变温度分别升高10℃和20℃左右,明显提高了复合材料的热稳定性能。

  12. Impact of regeneration process on the crystalline structure and enzymatic hydrolysis of cellulose obtained from ionic liquid.

    Science.gov (United States)

    Cao, Xuefei; Peng, Xinwen; Sun, Shaoni; Zhong, Linxin; Wang, Sha; Lu, Fachuang; Sun, Runcang

    2014-10-13

    The present study investigated the impact of regeneration process on the crystalline structure and enzymatic hydrolysis behaviors of microcrystalline cellulose (MCC) regenerated from ionic liquid 1-butyl-3-methylimidazolium chloride. The crystalline structures of these regenerated samples were analyzed by X-ray diffraction. Results suggested that almost amorphous cellulose was obtained by regenerating MCC in acetone (DRC-a), while partial cellulose II structure could be found in these regenerated samples from water and ethanol. Additionally, the enzymatic hydrolysis behaviors of MCC and its regenerated samples were comparatively studied. Results showed that above 90% of cellulose could be converted into glucose within 4h for DRC-a and regenerated cellulose without drying (WRC-w) as compared to that of MCC (9.7%). Therefore, the regeneration process could significantly influence the crystallinity and digestibility of cellulose. Copyright © 2014 Elsevier Ltd. All rights reserved.

  13. Microfibrillated cellulose and new nanocomposite materials: a review

    DEFF Research Database (Denmark)

    Siró, Istvan; Plackett, David

    2010-01-01

    Due to their abundance, high strength and stiffness, low weight and biodegradability, nano-scale cellulose fiber materials (e.g., microfibrillated cellulose and bacterial cellulose) serve as promising candidates for bio-nanocomposite production. Such new high-value materials are the subject...... in order to address this hurdle. This review summarizes progress in nanocellulose preparation with a particular focus on microfibrillated cellulose and also discusses recent developments in bio-nanocomposite fabrication based on nanocellulose....

  14. 纤维素/海藻酸钠共混膜的制备及力学性能%Preparation and mechanical properties of cellulose/sodium alginate blend membranes

    Institute of Scientific and Technical Information of China (English)

    李娜; 刘文洁; 罗虎

    2013-01-01

    Cellulose and sodium alginate were separately dissolved in the blend system of sodium hydroxide,urea and thiourea to prepare cellulose and cellulose/sodium alginate blend membranes.The optimal process conditions of cellulose membrane were decided by orthogonal experiment and single factor experiment.The preparation technology of cellulose/sodium alginate blend membrane was also studied.The results showed that the membrane prepared from 4.5% cellulose solution by mass fraction had the optimal tensile strength of 5.2 MPa while coagulating in 5% sulfuric acid solution at 25 ℃ for 15 min and plasticizing in 20% glycerin solution for 30 min; and the obtained cellulose/sodium alginate blend membrane had the optimal tensile strength of 3.50 MPa when the process conditions were optimized as followed:the blend solution containing 4.5% cellulose and 3% sodium alginate by mass fraction at the mass ratio of 100/5,soaking in 5% sulfuric acid solution and reacting for 15 min,coagulating in 10% calcium chloride solution for 10 min,and plasticizing in 15% glycerin solution for 15 min.%将纤维素和海藻酸钠分别溶于氢氧化钠/尿素/硫脲体系,制得纤维素膜和纤维素/海藻酸钠共混膜,通过正交实验和单因素实验法分析,确定制备纤维素膜的最佳工艺条件,在此基础上研究了纤维素/海藻酸钠共混膜的制备工艺.结果表明:质量分数为4.5%的纤维素溶液所制得的膜在25℃的5%的硫酸溶液中凝固15 min,20%的甘油溶液中塑化30 min,其膜的拉伸强度较佳为5.2 MPa;纤维素/海藻酸钠共混膜的较佳工艺:质量分数分别为4.5%的纤维素溶液和3%的海藻酸钠溶液按质量比100/5共混后先浸入5%硫酸溶液中反应15 min,再放入10%氯化钙溶液中凝固10 min,用15%甘油溶液塑化15 min后,共混膜的拉伸强度达到3.50 MPa.

  15. Cellulose Insulation

    Science.gov (United States)

    1980-01-01

    Fire retardant cellulose insulation is produced by shredding old newspapers and treating them with a combination of chemicals. Insulating material is blown into walls and attics to form a fiber layer which blocks the flow of air. All-Weather Insulation's founders asked NASA/UK-TAP to help. They wanted to know what chemicals added to newspaper would produce an insulating material capable of meeting federal specifications. TAP researched the query and furnished extensive information. The information contributed to successful development of the product and helped launch a small business enterprise which is now growing rapidly.

  16. Base metal catalyzed graphitization of cellulose : A combined Raman spectroscopy, temperature-dependent X-ray diffraction and high-resolution transmission electron microscopy study

    NARCIS (Netherlands)

    Hoekstra, Jacco; Beale, Andrew M.; Soulimani, Fouad; Versluijs-Helder, Marjan; Geus, John W.; Jenneskens, Leonardus W.

    2015-01-01

    Microcrystalline cellulose (MCC) spheres homogeneously loaded with the nitrate salts of copper, nickel, cobalt, or iron are excellent model systems to establish the temperature at which highly dispersed base metal nanoparticles are formed as well as to establish the temperature at which catalytic gr

  17. Base metal catalyzed graphitization of cellulose : A combined Raman spectroscopy, temperature-dependent X-ray diffraction and high-resolution transmission electron microscopy study

    NARCIS (Netherlands)

    Hoekstra, Jacco; Beale, Andrew M.; Soulimani, Fouad; Versluijs-Helder, Marjan; Geus, John W.; Jenneskens, Leonardus W.

    2015-01-01

    Microcrystalline cellulose (MCC) spheres homogeneously loaded with the nitrate salts of copper, nickel, cobalt, or iron are excellent model systems to establish the temperature at which highly dispersed base metal nanoparticles are formed as well as to establish the temperature at which catalytic gr

  18. Carrier mobility, band tails and defects in microcrystalline silicon

    Science.gov (United States)

    Reynolds, Steve

    2010-11-01

    The development of microcrystalline silicon thin films and devices is briefly reviewed. Transport mechanisms, and the attendant key parameters of carrier mobility, band-tail width and defect density, are linked to film structure and composition. In particular we discuss the wide (but systematic) variations in time-of-flight mobility and its unusual field-dependence. While microcrystalline silicon remains an inferior semiconductor to single-crystal silicon, we propose, and support by means of a computer model, that present device-grade material may be of sufficient quality to justify re-examining whether useful thin-film bipolar devices might be developed. These could find application as more sensitive photo-detectors, and as current drivers in organic LED displays and logic circuits.

  19. Effect of Mixed Solvents Consisting of Water and Organic Solvent on Preparation of Medium-Responsive Grafted Cellulose Film by Means of Photografting

    Directory of Open Access Journals (Sweden)

    Irwan Ginting-Suka

    2006-11-01

    Full Text Available Cellulose having a medium-responsive function were synthesized by photografting of methacrylic acid (MAA on regenerated cellulose film (thickness = 20 µm at 60°C using mixed solvent consisting of water and organic solvents such as acetone and methanol. Xanthone was used as photoinitiator by coating on the film surfaces. A maximum percentage of grafting was observed at a certain concentration of organic solvent. MAA-grafted cellulose films produced showing homogeneous distribution of grafted chains, which was examined by scanning electron microscopy. The modified films also exhibit medium responsive character, it shrinks in acidic and swells in basic solution. Moreover, the grafted film exhibited the ability to absorb copper ion, which was not influenced by the solvent used in grafting processes.

  20. 三醋酸纤维素/醋酸纤维素正渗透膜的制备工艺对性能的影响%Performance Effects on Preparation Process of Cellulose Triacetate/Cellulose Acetate Forward Osmosis Membrane

    Institute of Scientific and Technical Information of China (English)

    曾瑜; 宗同强; 赖华杰; 李娜; 靳焘

    2016-01-01

    Series of osmosis membrane were prepared by phase inversion method with cellulose acetate and cellulose triacetate as membrane materials, and explored three important factors affecting water flux of forward osmosis membranes:The thickness of membrane, the gel time and the heat treatment process. The results show that the best technological conditions for preparing forward osmosis membrane is that the thickness is 300mm, gel time is 48 h and through heat treatment process. The water flux of forward osmosis prepared by these technological conditions reach 7.088 L/m2·h.%通过相转变法制备了一系列三醋酸纤维素/醋酸纤维素正渗透膜,并探索了影响正渗透膜水通量的三个重要因素:膜厚度、凝胶时间、热处理过程。结果表明膜厚度为300mm、凝胶时间48 h,并经过热处理以后的正渗透膜水通量效果最佳,达到7.088 L/m2·h。

  1. Identification of microcrystalline rocks using thermal emission spectroscopy

    Science.gov (United States)

    Hardgrove, C. J.; Rogers, D.; Glotch, T. D.; Arnold, J. A.

    2015-12-01

    High-silica deposits on Mars have been discovered from orbit (Holden Crater, Mawrth Vallis) and from landed surface missions to both Gusev Crater (Spirit) and Gale Crater (Curiosity). The character of these silica deposits can be used to understand both the depositional environment (i.e. fumarole vs. sinter) and/or diagenetic process. Initial work has shown that, in the case of opaline silica, there are differences in spectral shape that may be related to surface textural features imparted during formation or post-depositional alteration. Due to the increasing importance of understanding microcrystalline deposits on Mars, here, we study the effects of crystal size and surface roughness on thermal infrared emission spectra of micro- and macro-crystalline quartz. The spectra of chert and macro-crystalline quartz have significant differences in both spectral contrast, and in the rounded doublet between ~1000-1250 cm-1, which can shift and appear less rounded in microcrystalline samples. We find that microcrystalline minerals exhibit naturally rough surfaces compared to their macrocrystalline counterparts at the 10 micron scale; and that this roughness causes distinct spectral differences within the Reststrahlen bands. We find that surface roughness, if rough on the scale of the wavelengths where the wavelength-dependent absorption coefficient (k) is large, can cause not only decreased spectral contrast, but also substantial changes in spectral shape. The spectral shape differences are small enough that the composition of the material is still recognizable, but large enough such that a roughness effect could be detected. We find that my studying the thermal infrared spectral character of the sample, it may be possible to make general inferences about microcrystallinity, and thus aid in the potential reconstruction of sedimentary rock diagenesis.

  2. 离子液体法制备再生纤维素/角蛋白共混膜的研究%Research of Regenerated Cellulose/Keratin Blend Membranes Prepared from Ionic Liquids

    Institute of Scientific and Technical Information of China (English)

    张猛; 马博谋; 何春菊

    2013-01-01

    合成了离子液体1-丁基-3-甲基咪唑氯盐([BMIM]Cl),以其为溶剂溶解羊毛角蛋白和纤维素,并制得再生纤维素/角蛋白共混膜.通过扫描电子显微镜(SEM)、傅里叶红外光谱仪(FT-IR)、热失重分析仪(TGA)及强度测试仪等对共混膜的性能进行表征.测试结果表明:与单一原料组分相比,共混膜具有较高的热稳定性,但力学性能有所降低,此外,羊毛角蛋白再生前后的结构并未发生显著变化.%l-butyl-3-methylimidazolium chloride ([BMIM] CD was synthesized to dissolve wool keratin and cellulose, and the keratin/cellulose blend membranes were prepared. The properties of the membrane were evaluated through scanning electron microscope (SEM), Fourier transforms infrared (FT-IR), thermogravimetric analyzer (TGA) and tension strength tester. All the results showed that the blend membranes presented better thermal stability than that of raw cellulose and keratin, but inferior mechanical property. The structure of wool keratin didn't have remarkable change after regeneration.

  3. Use of agroindustrial waste in the preparation of nanocomposites based on bacterial cellulose and hydroxyapatite; Utilizacao de residuos agroindustriais na elaboracao de bionanocompositos baseados em celulose bacteriana e hidroxiapatita

    Energy Technology Data Exchange (ETDEWEB)

    Duarte, Eden B.; Chagas, Bruna S. das; Feitosa, Judith P.A. [Universidade Federal do Ceara (UFC), Fortaleza, CE (Brazil); Andrade, Fabia K.; Borges, Maria F.; Muniz, Celli R.; Souza Filho, Men de Sa M.; Rosa, Morsyleide F., E-mail: morsyleide.rosa@embrapa.br [Embrapa Agroindustria Tropical, Fortaleza, CE (Brazil); Brigida, Ana I. [Embrapa Agroindustria de Alimentos, Barra de Guaratiba, Rio de Janeiro, RJ (Brazil); Morais, Joao P.S. [Embrapa Algodao, Campina Grande, PB (Brazil)

    2013-07-01

    Environmental issues have supported the interest in renewable sources and agroindustrial residues became a significant resource for the production of new materials. The present work presents the use of agroindustrial residues to obtain bacterial cellulose (BC) for further elaboration of nanocomposites with hydroxyapatite (HA). The production of BC membranes occurred in Hestrin & Schramm medium, cashew juice and sisal liquid waste cultivated under static conditions. After the incubation period, the BC membranes were purified and nanocomposites prepared by successive immersion of the purified membranes in solutions of Calcium Chloride (CaCl{sub 2}), and Sodium Phosphate (Na{sub 2}HPO{sub 4}), followed by drying and subsequent characterization. The materials obtained were characterized by Thermogravimetric Analysis (TGA) and X-ray Diffraction (XRD). Additionally, in vitro tests were performed for nanocomposites. The results showed the production of cellulose from the three substrates studied, without the need for further supplementation or pH change. In all characterizations, structure and typical behavior of bacterial cellulose were found. The composites showed bioactivity and the adsorption capacity of proteins, which lead to potential biocompatibility of these materials. (author)

  4. Preparation and characterization of paper based nano cellulose PU synthetic leather%纸基纳米纤维素PU合成革的制备与研究

    Institute of Scientific and Technical Information of China (English)

    颜明; 宋冰; 石勇; 王伟; 周小凡

    2016-01-01

    with plant fiber paper as raw material, ZnCl2 solution was used as the solvent of cellulose, ifber substrate was prepared by sol-gel method, it was studied that effects of dissolution time of paper ifber in ZnCl2 solution at 80℃, aging time, plasticizing agent and drying on substrate performance and on the physical and mechanical properties of synthetic leather. The results showed that the physical properties of the substrate is the best when the dissolution time is 8s in ZnCl2 solution at 80℃, aging time in air 2h, 30% amino silicone oil emulsion as a plasticizer, and by freeze drying. The moisture permeability, tensile strength, break elongation of the synthetic leather made with the leather substrate was close to natural leather. The substrate base, paper and the synthetic leather were characterized by scanning electron microscopy.%以植物纤维纸张为原料,ZnCl2溶液为纤维素溶剂,通过溶胶-凝胶法制备凝胶纤维基材,研究了Z n C l2溶液在80℃对纤维纸张的溶解时间、老化时间、增塑剂的选择和干燥方式对基材性能的影响以及合成革物理机械性能的影响。结果表明:Z n C l2溶液在80℃对纤维纸张的溶解8s、空气中老化2h,选择30%的氨基硅油乳液作为增塑剂、干燥方式为冷冻干燥时,基材的物理性能最佳。此基材制备的合成革的透湿性能,抗张强度,断裂伸长率都较接近天然皮革。通过扫描电镜对基材、原纸和合成革进行表征。

  5. Analysis on chemical components changes in preparation process of cellulosic ethanol from poplar wood%杨木制备纤维乙醇过程中化学成分变化的分析

    Institute of Scientific and Technical Information of China (English)

    闫兴伟; 崔琳; 张林; 王芳; 陈茜文

    2015-01-01

    杨树是我国重要的速生树种。以杨木为原料制备生物乙醇是解决当今能源问题的一项新的尝试。对杨木原料蒸汽爆破预处理后以及菌处理后的化学成分及化学性质进行了测定分析。通过对比其化学成分(纤维素、木素、半纤维素、抽出物、灰分及蛋白质)的变化,研究了以杨木为原料制备生物乙醇生产过程中化学成分变化机理,旨在为指导杨木制备木质纤维乙醇的生产,并为发酵后副产物的回收再利用提供理论依据。%Poplar is an important fast-growing species in China. The preparation of bio-ethanol with poplar wood as the raw material is a new attempt to solve today’s energy problems. After steam-exploded pretreatment and then bacteria treatment to the poplar wood raw materials, the materials’ chemical composition and properties were measured and analyzed. Through contrasting the changes of the materials’ chemical composition(cellulose, lignin, hemicelluloses, extracts, ash and protein), the mechanism of chemical change of the tested materials in the bioethanol production process prepared from poplar wood was studied, the surplus product contained 64.07%lignin, 6.78% cellulose and 6.88% hemicellulose. The results provide a theoretical basis for guiding the preparation of poplar wood cellulosic ethanol production, and the subsequent recycling of fermentation by-products.

  6. Research Progress of the Preparation and Application of Cellulose/Chitosan Composite Materials%纤维素/壳聚糖复合材料的制备与应用研究进展

    Institute of Scientific and Technical Information of China (English)

    付冉冉; 程博闻; 纪秀杰; 任燕飞; 杨丽云; 汪港; 费鹏飞

    2016-01-01

    纤维素/壳聚糖复合材料利用纤维素提高了共混材料的力学性能,同时保持了壳聚糖优良的生物相容性和抗菌性,无毒无污染。但是二者分子内和分子间含有大量的氢键,使得在水和常规有机溶剂中很难溶解,限制了复合材料的加工和应用,离子液体的出现为二者的溶解和复合提供了新的思路。综述了纤维素/壳聚糖复合材料的制备方法、制备体系及在工业吸附、生物医疗、食品包装和纺织工业领域的应用,重点介绍了离子液体在此复合材料制备过程中的应用,以为纤维素/壳聚糖复合材料的制备工艺和应用发展提供参考。%The cellulose/chitosan composite can improve the mechanical properties of the blend material due to the cellulose,while maintains the good biocompatibility and antimicrobial properties of chitosan.The composite are non-toxic and pollution-free.However,cellulose and chitosan are difficult to dissolve in water and conventional orga-nic solvents,because of its large proportion of intramolecular and intermolecular hydrogen bonds,which strictly limit its processing and applications.The presence of the ionic liquid provides a new approach for the composite.This re-view aims to summarize the preparation method,preparation system of cellulose/chitosan composite materials and its application in industrial adsorption,biomedical,food packaging and textile industry,with emphasis on the application of ionic liquid in the fabrication of the composite.This paper is expected to provide a reference for the development of fabrication and application of cellulose/chitosan composite.

  7. Preparation, Characterization and Solubility of Alkali Soluble Hydroxyethyl Cellulose%碱溶性羟乙基纤维素的合成、表征及溶解性能

    Institute of Scientific and Technical Information of China (English)

    花影; 李发学; 胡盼盼; 刘兆峰; 俞建勇

    2012-01-01

    As one of the cellulose derivatives with low molar substitution (MS), hydroxyethyl cellulose (HEC) which possesses unique property of alkali solubility was synthesized by the gas-solid reaction of raw cellulose and ethylene oxide (EO). The MS and micromorphology structure of the prepared HEC were characterized by Fourier transform infrared spectroscopy(FT-IR) , 1H NMR and X-ray diffraction techniques. The effects of etherification on the properties of HEC were discussed by dissolution property test. Experimental results showed that with the increase of the mass ratio of EO to raw cellulose the MS of HEC increased, the crystallinity of HEC decreased and the solubility increased, while the viscosity of the solution declined nonlinearly.%采用环氧乙烷(EO)与原始纤维素的气固相反应,成功制备了具有独特碱溶解性能的低摩尔取代度(MS)羟乙基纤维素(HEC).利用傅里叶变换红外光谱(FT-IR)、核磁共振氢谱(1H-NMR)和X射线衍射分析方法,表征了HEC的微观结构和摩尔取代度,并通过测试HEC的溶解性能,探讨醚化对纤维素溶解性能的影响.结果表明:随EO与原始纤维素质量比的增加,HEC的摩尔取代度增大,结晶度减小,溶解度增大,溶液黏度呈非线性下降.

  8. Cytocompatible cellulose hydrogels containing trace lignin.

    Science.gov (United States)

    Nakasone, Kazuki; Kobayashi, Takaomi

    2016-07-01

    Sugarcane bagasse was used as a cellulose resource to prepare transparent and flexible cellulose hydrogel films. On the purification process from bagasse to cellulose, the effect of lignin residues in the cellulose was examined for the properties and cytocompatibility of the resultant hydrogel films. The cellulose was dissolved in lithium chloride/N,N-dimethylacetamide solution and converted to hydrogel films by phase inversion. In the purification process, sodium hydroxide (NaOH) treatment time was changed from 1 to 12h. This resulted in cellulose hydrogel films having small amounts of lignin from 1.62 to 0.68%. The remaining lignin greatly affected hydrogel properties. Water content of the hydrogel films was increased from 1153 to 1525% with a decrease of lignin content. Moreover, lower lignin content caused weakening of tensile strength from 0.80 to 0.43N/mm(2) and elongation from 45.2 to 26.5%. Also, similar tendency was observed in viscoelastic behavior of the cellulose hydrogel films. Evidence was shown that the lignin residue was effective for the high strength of the hydrogel films. In addition, scanning probe microscopy in the morphological observation was suggested that the trace lignin in the cellulose hydrogel affected the cellulose fiber aggregation in the hydrogel network. The trace of lignin in the hydrogels also influenced fibroblast cell culture on the hydrogel films. The hydrogel film containing 1.68% lignin showed better fibroblast compatibility as compared to cell culture polystyrene dish used as reference.

  9. Impact of ionic liquid pretreatment conditions on cellulose crystalline structure using 1-ethyl-3-methylimidazolium acetate.

    Science.gov (United States)

    Cheng, Gang; Varanasi, Patanjali; Arora, Rohit; Stavila, Vitalie; Simmons, Blake A; Kent, Michael S; Singh, Seema

    2012-08-23

    Ionic liquids (ILs) have been shown to affect cellulose crystalline structure in lignocellulosic biomass during pretreatment. A systematic investigation of the swelling and dissolution processes associated with IL pretreatment is needed to better understand cellulose structural transformation. In this work, 3-20 wt % microcrystalline cellulose (Avicel) solutions were treated with 1-ethyl-3-methylimidazolium acetate ([C(2)mim][OAc]) and a mixture of [C(2)mim][OAc] with the nonsolvent dimethyl sulfoxide (DMSO) at different temperatures. The dissolution process was slowed by decreasing the temperature and increasing cellulose loading, and was further retarded by addition of DMSO, enabling in-depth examination of the intermediate stages of dissolution. Results show that the cellulose I lattice expands and distorts prior to full dissolution in [C(2)mim][OAc] and that upon precipitation the former structure leads to a less ordered intermediate structure, whereas fully dissolved cellulose leads to a mixture of cellulose II and amorphous cellulose. Enzymatic hydrolysis was more rapid for the intermediate structure (crystallinity = 0.34) than for cellulose II (crystallinity = 0.54).

  10. Effect of cooking temperature on the crystallinity of acid hydrolysed-oil palm cellulose

    Science.gov (United States)

    Kuthi, Fatin Afifah Binti Ahmad; Badri, Khairiah Haji

    2014-09-01

    In this research, we studied the effect of acid hydrolysis temperature on the crystallinity of cellulose produced from empty fruit bunch (EFB). The hydrolysis temperature was studied from 120 to 140 °C at a fixed time and sulfuric acid, H2SO4 concentration which were 1 h and 1% (v/v) respectively. X-ray diffractometry (XRD) was carried out to measure the crystallinity of cellulose produced at varying hydrolysis temperatures. During hydrolysis, the amorphous region of α-cellulose was removed and the crystalline region was obtained. Percentage of crystallinity (CrI) for acid hydrolysed cellulose at 120, 130 and 140 °C were 54.21, 50.59 and 50.55 % respectively. Morphological studies using scanning electron microscope (SEM) showed that acid hydrolysis defibrilised to microfibrils in α-cellulose. The extraction process to produce α-cellulose has also been successfully carried out as the impurities at the outer surface, lignin and hemicellulose were removed. These findings were supported by the disappearance of peaks at 1732, 1512 and 1243 cm-1 on Fourier Transform infrared (FTIR) spectrum of α-cellulose. Similar peaks were identified in both the commercial microcrystalline cellulose (C-MCC) and acid hydrolysed cellulose (H-EFB), indicating the effectiveness of heat-catalysed acid hydrolysis.

  11. Nanomechanics of cellulose crystals and cellulose-based polymer composites

    Science.gov (United States)

    Pakzad, Anahita

    Cellulose-polymer composites have potential applications in aerospace and transportation areas where lightweight materials with high mechanical properties are needed. In addition, these economical and biodegradable composites have been shown to be useful as polymer electrolytes, packaging structures, optoelectronic devices, and medical implants such as wound dressing and bone scaffolds. In spite of the above mentioned advantages and potential applications, due to the difficulties associated with synthesis and processing techniques, application of cellulose crystals (micro and nano sized) for preparation of new composite systems is limited. Cellulose is hydrophilic and polar as opposed to most of common thermoplastics, which are non-polar. This results in complications in addition of cellulose crystals to polymer matrices, and as a result in achieving sufficient dispersion levels, which directly affects the mechanical properties of the composites. As in other composite materials, the properties of cellulose-polymer composites depend on the volume fraction and the properties of individual phases (the reinforcement and the polymer matrix), the dispersion quality of the reinforcement through the matrix and the interaction between CNCs themselves and CNC and the matrix (interphase). In order to develop economical cellulose-polymer composites with superior qualities, the properties of individual cellulose crystals, as well as the effect of dispersion of reinforcements and the interphase on the properties of the final composites should be understood. In this research, the mechanical properties of CNC polymer composites were characterized at the macro and nano scales. A direct correlation was made between: - Dispersion quality and macro-mechanical properties - Nanomechanical properties at the surface and tensile properties - CNC diameter and interphase thickness. Lastly, individual CNCs from different sources were characterized and for the first time size-scale effect on

  12. Formation of membranes by means of immersion precipitation : Part II. the mechanism of formation of membranes prepared from the system cellulose acetate-acetone-water

    NARCIS (Netherlands)

    Reuvers, A.J.; Smolders, C.A.

    1987-01-01

    Using equations and boundary conditions derived in Part I1, calculations have been performed on the ternary diffusion processes that occur in a cellulose acetate (CA) -acetone casting solution immersed into a water bath. The necessary concentration-dependent thermodynamic and hydrodynamic parameters

  13. Nanocellulose-based biosensors: design, preparation, and activity of peptide-linked cotton cellulose nanocrystals having fluorimetric and colorimetric elastase detection sensitivity

    Science.gov (United States)

    Nanocrystalline cellulose is an amphiphilic, high surface area material that can be easily functionalized and is biocom-patible and eco-friendly. It has been used singularly and in combination with other nanomaterials to optimize biosensor design. The attachment of peptides and proteins to nanocryst...

  14. Preparation of Nano-crystalline Cellulose from Pineapple Leaf Fiber%菠萝叶纤维制备纳米纤维素晶体的研究

    Institute of Scientific and Technical Information of China (English)

    陈红莲; 高天明; 郑龙; 廖建和; 黄茂芳

    2012-01-01

    菠萝叶纤维经过氢氧化钠预处理、硫酸水解制备得到纳米纤维素晶体(NCC),再用扫描电镜(SEM)、傅立叶转换红外光谱仪(FTIR)、热重(TG)分析仪和X-射线衍射分析仪(XRD)对其结构和性能进行表征和分析.结果表明,NCC晶体颗粒尺寸为30~50 nm;红外光谱证明非纤维素部分有效去除;NCC晶型仍属于纤维素Ⅰ,结晶度从75.9%提高到87.5%;比起原纤维,NCC的降解温度明显降低.%Pineapple leaf fiber (PALF)was pretreated by sodium hydroxide, and hydrolyzed by sulfuric acid, then the nano-crystalline cellulose(NCC)was gotten. We characterized the structure and properties of NCC by SEM,FTIR, TG and XRD. The results showed that the size of NCC is 30~50 nm, non-cellulose was eliminated effectively, crystalline cellulose type of NCC is cellulose I, degree of crystallinity rises from 75.9% to 87.5%, and compared to the original fiber, the degradation temperature decreases clearly.

  15. Preparation and Characterization of Nitrated Bacterial Cellulose%硝化细菌纤维素的制备及表征

    Institute of Scientific and Technical Information of China (English)

    杨强; 彭碧辉; 梁岗; 罗庆平; 裴重华

    2012-01-01

    Nitrated bacterial cellulose (NBC) was synthesized from bacterial cellulose(BC) by nitric-sulfuric acid method. The results showed that the network structure of BC were not obviously degraded by this method and the stability of nitrated bacterial cellulose reached the standard for A degree of nitrocellulose. The thermal decomposition activation energy calculated by differential scanning calorimetry results is 212. 53 kJ/mol,and the thermal stability of nitrated bacterial cellulose is better than nitrocellulose.%以细菌纤维素为原料,用硝硫混酸法合成出硝化细菌纤维素(NBC).结果表明,采用硝硫混酸法合成硝化细菌纤维素未造成细菌纤维素的网状结构明显断裂降解,且合成出的硝化细菌纤维素安定性能达到A级硝化纤维素标准.用差示扫描量热法对产物进行了表征,并计算出硝化细菌纤维素的热分解活化能为212.53 kJ/mol,表明硝化细菌纤维素热的稳定性优于硝化棉.

  16. 熔融制粒法制备盐酸二甲双胍缓释片%Preparation of Metformin Hydrochloride Sustained-release Tablets By Melt Granulation

    Institute of Scientific and Technical Information of China (English)

    许谙; 孙丹青

    2013-01-01

    OBJECTIVE To prepare metformin hydrochloride sustained-release tablets and to study its release characterization in vitro and the factors affecting drug release.METHODS Metformin hydrochloride sustained-release tablets were prepared with glycery behenate as matrix material,microcrystalline cellulose as pore-forming agent by melt granulation.The impacts of releasing transmitter,contents of glycery behenate and microcrystalline cellulose,and preparation process factors on the drug release in vitro of the tablets were studied.RESULTS The contents of glycery behenate and microcrystalline cellulose were critical factors affecting drug release rate.The tablets had a remarkable sustained-release property,the drug release profile in vitro followed zero order or Higuchi kinetics.CONCLUSION Using glycery behenate as the wax matrix material,combining with other filers,a sustained release tablet of once daily administration is prepared by melt granulation.%目的 制备盐酸二甲双胍缓释片,并考察其释药行为及影响因素.方法 以山嵛酸甘油酯为骨架材料,微晶纤维素为致孔剂,采用熔融制粒技术制备盐酸二甲双胍缓释片,并考察不同释放介质,山嵛酸甘油酯、微晶纤维素的不同用量以及制备工艺参数等对该缓释片体外释放的影响.结果 山嵛酸甘油酯和微晶纤维素的用量为药物释放的主要影响因素,制备的缓释片具有明显的缓释特征,体外释药过程符合零级动力学模型.结论 采用山嵛酸甘油酯作为蜡质骨架材料,结合其他辅料,采用熔融制粒技术可制备日服1次的盐酸二甲双胍缓释片.

  17. Whey protein aerogel as blended with cellulose crystalline particles or loaded with fish oil.

    Science.gov (United States)

    Ahmadi, Maede; Madadlou, Ashkan; Saboury, Ali Akbar

    2016-04-01

    Whey protein hydrogels blended with nanocrystalline and microcrystalline cellulose particles (NCC and MCC, respectively) were prepared, followed by freeze-drying, to produce aerogels. NCC blending increased the Young's modulus, and elastic character, of the protein aerogel. Aerogels were microporous and mesoporous materials, as characterized by the pores sizing 1.2 nm and 12.2 nm, respectively. Blending with NCC decreased the count of both microporous and mesoporous-classified pores at the sub-100 nm pore size range investigated. In contrast, MCC blending augmented the specific surface area and pores volume of the aerogel. It also increased moisture sorption affinity of aerogel. The feasibility of conveying hydrophobic nutraceuticals by aerogels was evaluated through loading fish oil into the non-blended aerogel. Oil loading altered its microstructure, corresponding to a peak displacement in Fourier-transform infra-red spectra, which was ascribed to increased hydrophobic interactions. Surface coating of aerogel with zein decreased the oxidation susceptibility of the loaded oil during subsequent storage.

  18. Development of nonflammable cellulosic foams

    Science.gov (United States)

    Luttinger, M.

    1972-01-01

    The development of a moldable cellulosic foam for use in Skylab instrument storage cushions is considered. Requirements include density of 10 lb cu ft or less, minimal friability with normal handling, and nonflammability in an atmosphere of 70 percent oxygen and 30 percent nitrogen at 6.2 psia. A study of halogenated foam components was made, including more highly chlorinated binders, halogen-containing additives, and halogenation of the cellulose. The immediate objective was to reduce the density of the foam through reduction in inorganic phosphate without sacrificing flame-retarding properties of the foams. The use of frothing techniques was investigated, with particular emphasis on a urea-formaldehyde foam. Halogen-containing flame retardants were deemphasized in favor of inorganic salts and the preparation of phosphate and sulphate esters of cellulose. Utilization of foam products for civilian applications was also considered.

  19. Exploring the effect of cellulose nanowhiskers isolated from oil palm biomass on polylactic acid properties.

    Science.gov (United States)

    Haafiz, M K Mohamad; Hassan, Azman; Khalil, H P S Abdul; Fazita, M R Nurul; Islam, Md Saiful; Inuwa, I M; Marliana, M M; Hussin, M Hazwan

    2016-04-01

    In this work, polylactic acid (PLA) reinforced cellulose nanowhiskers (CNW) were prepared through solution casting technique. The CNW was first isolated from oil palm empty fruit bunch microcrystalline cellulose (OPEFB-MCC) by using 64% H2SO4 and was designated as CNW-S. The optical microscopy revealed that the large particle of OPEFB-MCC has been broken down by the hydrolysis treatment. The atomic force microscopy confirmed that the CNW-S obtained is in nanoscale dimension and appeared in individual rod-like character. The produced CNW-S was then incorporated with PLA at 1, 3, and 5 parts per hundred (phr) resins for the PLA-CNW-S nanocomposite production. The synthesized nanocomposites were then characterized by a mean of tensile properties and thermal stability. Interestingly to note that incorporating of 3 phr/CNW-S in PLA improved the tensile strength by 61%. Also, CNW-S loading showed a positive impact on the Young's modulus of PLA. The elongation at break (Eb) of nanocomposites, however, decreased with the addition of CNW-S. Field emission scanning electron microscopy and transmission electron microscopy revealed that the CNW-S dispersed well in PLA at lower filler loading before it started to agglomerate at higher CNW-S loading (5phr). The DSC analysis of the nanocomposites obtained showed that Tg,Tcc and Tm values of PLA were improved with CNW-S loading. The TGA analysis however, revealed that incopreated CNW-S in PLA effect the thermal stability (T10,T50 and Tmax) of nanocomposite, where it decrease linearly with CNW-S loading.

  20. Some aspects of acetylation of untreated and mercerized sisal cellulose

    Energy Technology Data Exchange (ETDEWEB)

    Ciacco, Gabriela T.; Morgado, Daniella Lury; Frollini, Elisabete [Universidade de Sao Paulo, Sao Carlos (USP), SP (Brazil). Inst. de Quimica; Possidonio, Shirley; El Seoud, Omar A. [Universidade de Sao Paulo (USP), SP (Brazil). Inst. de Quimica

    2010-07-01

    We report here on some aspects of the acetylation in LiCl/N,N-dimethylacetamide, DMAc, of untreated and mercerized sisal cellulose, hereafter designated as sisal and M-sisal, respectively. Fiber mercerisation by NaOH solution has resulted in the following changes: 29.9% decrease in the index of crystallinity; 16.2% decrease in the degree of polymerization and 9.3% increase in a-cellulose content. A light scattering study of solutions of sisal, M-sisal, microcrystalline and cotton celluloses in LiCl/DMAc has shown that they are present as aggregates, with (an apparent) average aggregation numbers of 5.2, 3.2, 9.8, and 35.3, respectively. The presence of these aggregates affects the accessibility of cellulose during its functionalization. A study of the evolution of the degree of substitution, DS, of cellulose acetate as a function of reaction time showed an increase up to 5 h, followed by a decrease at 7 h. Possible reasons for this decrease are discussed. As expected, M-sisal gave a higher DS that its untreated counterpart. (author)

  1. Nanocellulose 3, 5-Dimethylphenylcarbamate Derivative Coated Chiral Stationary Phase: Preparation and Enantioseparation Performance.

    Science.gov (United States)

    Zhang, Xiaoli; Wang, Litao; Dong, Shuqing; Zhang, Xia; Wu, Qi; Zhao, Liang; Shi, Yanping

    2016-05-01

    Nanocrystalline cellulose (NCC) with high surface area and high ordered crystalline structure was prepared from microcrystalline cellulose (MCC) under the hydrolysis of sodium hypochlorite. NCC was further reacted with 3,5-dimethylphenyl isocyanate to obtain the nanocellulose derivative, and then coated successfully on the surface of silica gel to a prepared NCC-coated chiral stationary phase (CSP) as a new kind of chiral separation material. Similarly, MCC derivative-coated CSP was also prepared as contrast. The chiral separation performance of NCC-based CSP was evaluated and compared with MCC-based CSP by high-performance liquid chromatography. Moreover, the effects of the alcohol modifiers, mobile phase additives, and flow rates on chiral separations were investigated in detail. The results showed that 10 chiral compounds were separated on NCC-based CSP with better peak shape and higher column efficiency than MCC-based CSP, which confirmed that NCC-based CSP was a promising packing material for the resolution of chiral compounds.Chirality 28:376-381, 2016. © 2016 Wiley Periodicals, Inc.

  2. Carbon-supported base metal nanoparticles: cellulose at work.

    Science.gov (United States)

    Hoekstra, Jacco; Versluijs-Helder, Marjan; Vlietstra, Edward J; Geus, John W; Jenneskens, Leonardus W

    2015-03-01

    Pyrolysis of base metal salt loaded microcrystalline cellulose spheres gives a facile access to carbon-supported base metal nanoparticles, which have been characterized with temperature-dependent XRD, SEM, TEM, ICP-MS and elemental analysis. The role of cellulose is multifaceted: 1) it facilitates a homogeneous impregnation of the aqueous base metal salt solutions, 2) it acts as an efficacious (carbonaceous) support material for the uniformly dispersed base metal salts, their oxides and the metal nanoparticles derived therefrom, and 3) it contributes as a reducing agent via carbothermal reduction for the conversion of the metal oxide nanoparticles into the metal nanoparticles. Finally, the base metal nanoparticles capable of forming metastable metal carbides catalytically convert the carbonaceous support into a mesoporous graphitic carbon material.

  3. Nitration of Wood Cellulose in HNO3/Organic Solvent Medium

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    A steam explosion pretreatment at various severities was applied to pure wood cellulose; the influences of steam pretreatment on the morphological structure, the hydrophilic property and viscosity-average molecular weight of cellulose were evaluated. The nitration of steam-exploded cellulose was carried out in the nitrating agent medium (HNO3/organic solvent). The performance indexes of nitrocellulose, prepared from original and steam exploded samples, were determined by using the polarized optical microscope. The results show that after pretreatment the reactivity of the three hydroxyl groups in anhydroglucose unit of cellulose is improved, and the nitrogen content and the uniformity of NC from steam exploded cellulose observably increas.

  4. Characterization of blend hydrogels based on plasticized starch/cellulose acetate/carboxymethyl cellulose synthesized by electron beam irradiation

    Science.gov (United States)

    Senna, Magdy M.; Mostafa, Abo El-Khair B.; Mahdy, Sanna R.; El-Naggar, Abdel Wahab M.

    2016-11-01

    Blend hydrogels based on aqueous solutions of plasticized starch and different ratios of cellulose acetate (CA) and carboxymethyl cellulose (CMC) were prepared by electron beam irradiation (EB). The blends before and after EB irradiation were characterized by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The physico-chemical properties of blend hydrogels prepared by electron beam irradiation were improved compared to unirradiated blends.

  5. Cellulose metabolism in plants.

    Science.gov (United States)

    Hayashi, Takahisa; Yoshida, Kouki; Park, Yong Woo; Konishi, Teruko; Baba, Kei'ichi

    2005-01-01

    Many bacterial genomes contain a cellulose synthase operon together with a cellulase gene, indicating that cellulase is required for cellulose biosynthesis. In higher plants, there is evidence that cell growth is enhanced by the overexpression of cellulase and prevented by its suppression. Cellulase overexpression could modify cell walls not only by trimming off the paracrystalline sites of cellulose microfibrils, but also by releasing xyloglucan tethers between the microfibrils. Mutants for membrane-anchored cellulase (Korrigan) also show a typical phenotype of prevention of cellulose biosynthesis in tissues. All plant cellulases belong to family 9, which endohydrolyzes cellulose, but are not strong enough to cause the bulk degradation of cellulose microfibrils in a plant body. It is hypothesized that cellulase participates primarily in repairing or arranging cellulose microfibrils during cellulose biosynthesis in plants. A scheme for the roles of plant cellulose and cellulases is proposed.

  6. Nano- and microcrystalline diamond deposition on pretreated WC-Co substrates: structural properties and adhesion

    Science.gov (United States)

    Fraga, M. A.; Contin, A.; Rodríguez, L. A. A.; Vieira, J.; Campos, R. A.; Corat, E. J.; Trava Airoldi, V. J.

    2016-02-01

    Many developments have been made to improve the quality and adherence of CVD diamond films onto WC-Co hard metal tools by the removing the cobalt from the substrate surface through substrate pretreatments. Here we compare the efficiency of three chemical pretreatments of WC-Co substrates for this purpose. First, the work was focused on a detailed study of the composition and structure of as-polished and pretreated substrate surfaces to characterize the effects of the substrate preparation. Considering this objective, a set of WC-9% Co substrates, before and after pretreatment, was analyzed by FEG-SEM, EDS and x-ray diffraction (XRD). The second stage of the work was devoted to the evaluation of the influence of seeding process, using 4 nm diamond nanoparticles, on the morphology and roughness of the pretreated substrates. The last and most important stage was to deposit diamond coatings with different crystallite sizes (nano and micro) by hot-filament CVD to understand fully the mechanism of growth and adhesion of CVD diamond films on pretreated WC-Co substrates. The transition from nano to microcrystalline diamond was achieved by controlling the CH4/H2 gas ratio. The nano and microcrystalline samples were grown under same time at different substrate temperatures 600 °C and 800 °C, respectively. The different substrate temperatures allowed the analysis of the cobalt diffusion from the bulk to the substrate surface during CVD film growth. Furthermore, it was possible to evaluate how the coating adhesion is affected by the diffusion. The diamond coatings were characterized by Raman spectroscopy, XRD, EDS, FEG-SEM, atomic force microscope and 1500 N Rockwell indentation to evaluate the adhesion.

  7. Hydrolysis of cellulose catalyzed by quaternary ammonium perrhenates in 1-allyl-3-methylimidazolium chloride.

    Science.gov (United States)

    Wang, Jingyun; Zhou, Mingdong; Yuan, Yuguo; Zhang, Quan; Fang, Xiangchen; Zang, Shuliang

    2015-12-01

    Quaternary ammonium perrhenates were applied as catalyst to promote the hydrolysis of cellulose in 1-allyl-3-methylimidazolium chloride ([Amim]Cl). The quaternary ammonium perrhenates displayed good catalytic performance for cellulose hydrolysis. Water was also proven to be effective to promote cellulose hydrolysis. Accordingly, 97% of total reduced sugar (TRS) and 42% of glucose yields could be obtained under the condition of using 5mol% of tetramethyl ammonium perrhenate as catalyst, 70μL of water, ca. 0.6mmol of microcrystalline cellulose (MCC) and 2.0g of [Amim]Cl as solvent under microwave irradiation for 30min at 150°C (optimal conditions). The influence of quaternary ammonium cation on the efficiency of cellulose hydrolysis was examined based on different cation structures of perrhenates. The mechanism on perrhenate catalyzed cellulose hydrolysis is also discussed, whereas hydrogen bonding between ReO4 anion and hydroxyl groups of cellulose is assumed to be the key step for depolymerization of cellulose. Copyright © 2015. Published by Elsevier Ltd.

  8. Cellulose nanofibrils aerogels generated from jute fibers.

    Science.gov (United States)

    Lin, Jinyou; Yu, Liangbo; Tian, Feng; Zhao, Nie; Li, Xiuhong; Bian, Fenggang; Wang, Jie

    2014-08-30

    In this work, we report the cellulose nanofibrils extracted from the pristine jute fibers via the pretreatments followed by the TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl radical)-mediated oxidation and mechanical disintegration. The effects of pretreatments by using the NaOH solution and dimethyl sulfoxide solvent on the fiber morphology and macro/micro-structures were investigated by polarizing microscope and synchrotron radiation wide/small-angle X-ray scattering (WAXS/SAXS). The cellulose nanofibrils exhibit a diameter ranging from 5 nm to 20 nm and a length of several micrometers, which have been assembled into cellulose aerogels by the lyophilization of as-prepared nanofibrils dispersions with various concentrations. The results indicated that the hierarchical structures of as-prepared cellulose aerogels were dependent on the dispersion concentrations. The WAXS results show that the typical cellulose aerogels are coexistence of cellulose I and cellulose II, which has a great promise for many potential applications, such as pharmaceutical, liquid filtration, catalysts, bio-nanocomposites, and tissue engineering scaffolds. Copyright © 2014 Elsevier Ltd. All rights reserved.

  9. Utilization of purified cellulose in fiber studies.

    Science.gov (United States)

    Penner, M H; Liaw, E T

    1990-01-01

    Purified cellulose-type fiber products are widely used in experimental nutrition. Their use in a broad spectrum of studies may potentially lead to the acceptance of the misconception that the various commercially available cellulose products are equivalent. In this paper we have attempted to show that this is not the case. The comparative structural data of Table 2 and the compositional data of Olsen et al provide examples which indicate that purified cellulose preparations should not necessarily be considered equivalent. Unfortunately, our current lack of understanding of how fibers are metabolized and how they may affect specific physiological parameters makes it difficult to determine which, if any, of the measurable structural and chemical properties will be of relevance for a given in vivo study. At present, it appears that researchers utilizing/evaluating the consequences of consuming a purified cellulose-type fiber would be prudent to provide at least a limited amount of data on the properties of the cellulose preparation used in their studies. The characterization of the cellulose product may be done by a variety of methods depending on the expertise of the laboratory. The methods and results discussed in this paper provide an example of the type of information which may be obtained from an in vitro characterization of cellulose products.

  10. Preparation and Characterization of Bacterial Cellulose/Chitosan Composite Porous Scaffold%细菌纤维素/壳聚糖复合多孔支架材料的制备与表征

    Institute of Scientific and Technical Information of China (English)

    蔡志江; 侯成伟

    2012-01-01

    利用细茵纤维素水凝胶膜和壳聚糖为原料,介绍了多孔复合支架的制备方法,并利用红外光谱、扫描电子显微镜、x射线衍射、元素分析及力学性能测试对多孔复合支架的特性进行了研究。结果表明,复合多孔支架的表面孔径变大、孔隙率下降,但依然呈三维网络结构;壳聚糖的加入有可能取代水分而与细菌纤维素分子链形成分子间相互作用,使细茵纤维素的链规整度下降,结晶度指数由0.82下降至0.61;力学性能有所下降,拉伸强度从140MPa下降至134MPa;这种复合多孔支架由于具有良好的生物相容性可以应用于生物医学领域,如辅料、组织工程支架等。%In this study,an novel composite porous scaffold has been successfully prepared by using bacterial cellulose gel and chitosan solution as raw materials.Properties of this bacterial cellulose/chitosan composite porous scaffold are investigated by Fourier transform infrared spectrum(FT-IR),scanning electron microscopy(SEM),X-ray diffraction(XRD),element analysis and tensile test.SEM images show that chitosan molecules are not only coated on the bacterial cellulose fibrils surface but also penetrate inside bacterial cellulose.It has very well interconnected porous network structure and large aspect surface.With introduction of chitosan,the crystal structure of bacterial cellulose becomes less regular and the crystallinity index tends to decrease from 0.82 to 0.61,which might be associated with strong interaction between bacterial cellulose and chitosan.Tensile test results indicate that tensile strength and the elongation at break tend to decrease from 140 MPa to 134 MPa and 6.7% to 4.6%,respectively.While the Young’s modulus has a slight increase from 3.65 GPa to 3.9 GPa.Since bacterial cellulose and chitosan both have good biocompatibility,this composite porous scaffold might have potential biomedical applications such as tissue

  11. Preparation and In Vitro-In Vivo Evaluation of Sustained-Release Matrix Pellets of Capsaicin to Enhance the Oral Bioavailability.

    Science.gov (United States)

    Zhang, Ya; Huang, Zhimin; Omari-Siaw, E; Lu, Shuang; Zhu, Yuan; Jiang, Dongmei; Wang, Miaomiao; Yu, Jiangnan; Xu, Ximing; Zhang, Weiming

    2016-04-01

    Capsaicin has multiple pharmacological activities including antioxidant, anticancer, and anti-inflammatory activities. However, its clinical application is limited due to its poor aqueous solubility, gastric irritation, and low oral bioavailability. This research was aimed at preparing sustained-release matrix pellets of capsaicin to enhance its oral bioavailability. The pellets comprised of a core of solid-dispersed capsaicin mixed with microcrystalline cellulose (MCC) and hydroxypropyl cellulose (HPMC) and subsequently coating with ethyl cellulose (EC) were obtained by using the technology of extrusion/spheronization. The physicochemical properties of the pellets were evaluated through scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and X-ray diffractometry (XRD). Besides, the in vitro release, in vivo absorption, and in vitro-in vivo correlation were also assessed. More importantly, the relative bioavailability of the sustained-release matrix pellets was studied in fasted rabbits after oral administration using free capsaicin and solid dispersion as references. The oral bioavailability of the matrix pellets and sustained-release matrix pellets of capsaicin was improved approximately 1.98-fold and 5.34-fold, respectively, compared with the free capsaicin. A good level A IVIVC (in vitro-in vivo correlation) was established between the in vitro dissolution and the in vivo absorption of sustained-release matrix pellets. All the results affirmed the remarkable improvement in the oral bioavailability of capsaicin owing to the successful preparation of its sustained-release matrix pellets.

  12. Modification of cellulose for high glucose generation.

    Science.gov (United States)

    Jiang, Xue; Gu, Jian; Tian, Xiuzhi; Li, Yali; Huang, Dan

    2012-01-01

    The influence of introduction of cyanuric chloride on glucose's yield (Y) in acid-catalyzed hydrolysis of microcrystalline cellulose (MCC) has been studied. The content of cyanuric chloride (C) in modified MCCs was determined by X-ray photoelectric spectroscopy. The chemical structures of modified MCCs were analyzed by Fourier transformation-infrared spectroscopy and cross polarization/magic angle spinning (13)C nuclear magnetic resonance. Crystal index (CI) and the ratio (R) representing the sum of content of (1 ̅10) and (110) to that of (200) were calculated based on diffraction intensity in wide angle X-ray diffraction (WAXD). Hydrolysis experiment and WAXD show that Y, CI and R vary with C. The modified MCC containing 3.9 mol% of cyanuric chloride has the highest Y, the highest R and the lowest CI. Variations of CI and R show that the chemical modification changed the proportion of crystal/amorphous and crystal planes, both of which influence glucose's generation in hydrolysis of cellulose.

  13. Numerical simulations for the effiency improvement of hybrid dye-microcrystalline silicon pin-solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Burdorf, Sven; Bauer, Gottfried Heinrich; Brueggemann, Rudolf [Institut fuer Physik, Carl von Ossietzky Universitaet, Oldenburg (Germany)

    2011-07-01

    Hybrid solar cells consisting of dye sensitizers incorporated in the i-layer of microcrystalline silicon pin solar cell have been proposed and even recently processed. The dye sensitizer molecules are embedded in the matrix and enhance the overall absorption of the dye-matrix system due to their high absorption coefficient in the spectral range interesting for photovoltaic applications. However, the charge transport properties of dyes are quite poor. Microcrystalline silicon on the other hand has acceptable charge transport properties, while the absorption, given a layer thickness in the micron range, is relatively poor. This contribution investigates the effiency improvement of hybrid dye-microcrystalline solar cells compared to pure microcrystalline solar cells by simulation. The results indicate that, under optimal conditions, the effiency can be improved by more than 20 % compared to a pure microcrystalline silicon cell. The thickness reduction for the hybrid system can be as large as 50 % for the same effiency.

  14. 纳米纤维素/天然橡胶复合材料的制备及表征%Preparation and Characterization of Nano -crystalline Cellulose/Natural Rubber (NCC/NR) Composites *

    Institute of Scientific and Technical Information of China (English)

    陈红莲; 高天明; 黄茂芳; 廖建和

    2012-01-01

    Blended natural rubber (NR) with different amount of nano - cellulose cellulose ( NCC ) were usea to prepare nano -crystalline cellulose/natural rubber (NCC/NR) composites. The resulting products were characterized by scanning electron microscopy ( SEM), mechanical property testing, thermo - gravimetric analysis and dynamic mechanical analysis(DMA). Results showed that NCC were homogeneously distributed throughout NR matrix, which led to the en- hancement on mechanical properties. Moreover, the storage modulus ( E' ) of composites went up with the increment of NCC loadings and loss factor (tang) decreases, and the addition of NCC had less impact on the thermal stability of NR matrix.%采用共混法制备不同比率含量的纳米纤维素/天然橡胶(NCC/NR)复合材料,通过扫描电镜、力学性能、热稳定性以及动态力学性能的测定分析表明:纳米纤维素能较均匀分散在橡胶基质中,对天然橡胶起到较好的补强效果,复合材料的储能模量逐步增大,损耗因子逐步减小,纳米纤维素的加入对天然橡胶的热稳定性影响不大。

  15. Preparation and Properties of Chitosan/Regenerated Cellulose Fiber Composites in 1-Butyl, 3-Methylimidazolium Chloride%[BMIM]Cl离子液体中壳聚糖/纤维素纤维的制备及性能

    Institute of Scientific and Technical Information of China (English)

    杨海静; 魏立纲; 李坤兰; 马英冲; 王少君; 安庆大; 平清伟; 余加?

    2011-01-01

    Adoption of wet molding technology and different proportion chitosan/regenerated cellulose fiber composites were prepared by directly blending chitosan powder and cellulose in l-butyl,3-methylimidazolium chloride ionic liquid at room temperature. The morphology, structure and other property of the fibers were characterized by Fourier transform infrared spectrum(FT-IR) , scanning electron microscope (SEM) and so on. The result shows that the mechanical properties, degree of orientation, crystallization and breaking strength are reduced with the increase of chitosan content in fiber composites. Cellulose fiber and chitosan can achieve a good micro-scale mixing while ionic liquid as co-solvent. The ionic liquid can eventually be completely dissolved from the material.%以[BMIM]Cl离子液体为溶剂,在可控的条件下,将棉纤维与壳聚糖进行共混,采用湿法成型技术,制备了不同质量比的壳聚糖/纤维素纤维复合材料.并通过力学测试、红外光谱(FT-IR)和扫描电镜(SEM)等手段对其结构、性能进行了分析.结果表明,随着壳聚糖加入量的增加,纤维的取向度和结晶度下降,纤维的断裂强度下降,复合纤维表面纤丝结构的有序性降低.离子液体作为棉纤维与壳聚糖的共溶剂,可以实现两种材料很好的微观尺度混合,并且离子液体最终可以完全从材料中溶出.

  16. Research on preparation of cellulose diacetate from invasive plant: Solidago Canadensis L.%入侵植物加拿大一枝黄花制备二醋酸纤维素研究

    Institute of Scientific and Technical Information of China (English)

    徐莲莲; 杨再福; 朱丹丹

    2013-01-01

    Solidago Canadensis L.is used as the raw material to prepare highly purified α-cellulose and cellulose diacetate(CDA).Result shows that the best liquid-solid ratio during activation is 1∶7,the optimum dosage of catalyst and acetic anhydride respectively is 9% ~ 11% and 550% during acetified reaction,the esterification time was 2 h,and the temperature was 50 ℃,and the best AA concentration is 70% during saponification,the best temperature of saponification was 80 ℃ and the time was 2 h.The result of FTIR and XRD analysis shows that the cellulose from Solidago Canadensis L.is acetylated partly,and the crystallinity of the production is decreasing.%利用加拿大一枝黄花(Solidago Canadensis L.)茎干为原料,提取高纯度α-纤维素浆粕,制备二醋酸纤维素(CDA),并对其制备工艺进行优化.结果表明,制备醋酸纤维素的工艺最优条件为:活化最佳液固比:1∶7,醋化过程催化剂最佳用量为9%~11%,醋酸酐用量为550%,醋化时间2h,温度为50℃,皂化过程醋酸最佳浓度为70%,皂化最佳温度80℃,时间2h.红外和X射线分析表明,加拿大一枝黄花纤维素的羟基被部分醋酸酯化,经过醋化和皂化后结晶度下降为29.88%.

  17. Analysis of Molecular Size Distributions of Cellulose Molecules during Hydrolysis of Cellulose by Recombinant Cellulomonas fimi β-1,4-Glucanases

    Science.gov (United States)

    Stålbrand, Henrik; Mansfield, Shawn D.; Saddler, John N.; Kilburn, Douglas G.; Warren, R. Antony J.; Gilkes, Neil R.

    1998-01-01

    Four β-1,4-glucanases (cellulases) of the cellulolytic bacterium Cellulomonas fimi were purified from Escherichia coli cells transformed with recombinant plasmids. Previous analyses using soluble substrates had suggested that CenA and CenC were endoglucanases while CbhA and CbhB resembled the exo-acting cellobiohydrolases produced by cellulolytic fungi. Analysis of molecular size distributions during cellulose hydrolysis by the individual enzymes confirmed these preliminary findings and provided further evidence that endoglucanase CenC has a more processive hydrolytic activity than CenA. The significant differences between the size distributions obtained during hydrolysis of bacterial microcrystalline cellulose and acid-swollen cellulose can be explained in terms of the accessibility of β-1,4-glucan chains to enzyme attack. Endoglucanases and cellobiohydrolases were much more easily distinguished when the acid-swollen substrate was used. PMID:9647802

  18. Some historical remarks on microcrystalline arthritis (gout and chondrocalcinosis

    Directory of Open Access Journals (Sweden)

    G. Pasero

    2012-01-01

    Full Text Available The history of microcrystalline arthritis only began in 1961 when Daniel McCarty and Joseph Lee Hollander demonstrated the presence of sodium monourate crystals in the synovial fluid of gouty patients. However, gout is a historical disease, thanks to the descriptions of Hippocrates, Caelius Aurelianus, Soranus of Ephesus and Araeteus of Cappadocia. The relationship between hyperuricemia and gout was first documented in the nineteenth century by Alfred Baring Garrod, who demonstrated deposits of uric acid crystals on a linen thread held dipped in acidified blood (the so-called “thread method”. Gout has always been considered a prerogative of the moneyed classes (arthritis divitum, and history is full of famous gouty personalities, including kings, emperors, popes, commanders, politicians, artists, writers, philosophers and scientists. Another form of microcrystalline arthritis, chondrocalcinosis, was identified as being a rheumatic disorder different from gout in the 1960s. As a specific clinical entity, it was first identified in 1958 by Dušan Žitnˇan and Štefan Sit’aj in a few Slovak families.

  19. Scientific Opinion on the re-evaluation of microcrystalline wax (E 905 as a food additive

    Directory of Open Access Journals (Sweden)

    EFSA Panel on Food Additives and Nutrient Sources added to Food (ANS

    2013-04-01

    Full Text Available Following a request from the European Commission, the Panel on Food Additives and Nutrient Sources added to Food (ANS was asked to deliver a scientific opinion on microcrystalline wax (E 905 when used as a food additive. Microcrystalline wax (E 905 is authorised quantum satis as a surface treatment agent on non-chocolate confectionery, chewing gum and decorations, coatings and fillings, except fruit based fillings. It is also permitted as a surface treatment of melons, papaya, mango and avocado. The substance was evaluated by the Scientific Committee on Food (SCF in 1990 and 1995 and by the Joint FAO/WHO Expert Committee on Food Additives (JECFA, the latest in 1995. The JECFA established a group ADI of 20 mg/kg bw/day for mineral oils, paraffins and microcrystalline waxes. The Panel noted that all mineral oil products accumulated in tissues in a dose- and time-dependent manner with the exception of microcrystalline waxes. The Panel concluded that there is no concern for genotoxicity from microcrystalline wax (E 905. The Panel also considered that the available toxicity studies with mineral hydrocarbons, closely related from a chemical point of view with microcrystalline waxes, consistently reported no effects of concern associated with the intake of microcrystalline wax. The Panel further concluded that since no long-term toxicity and carcinogenicity studies with microcrystalline wax E 905 were available, no ADI could be established. The Panel also concluded that the conservative exposure estimates to microcrystalline wax (E 905 from its use at maximum permitted level (following quantum satis rules, resulted in a sufficient margin of safety compared to the NOAEL established by the Panel for the closely related high viscosity mineral oils, and therefore the use microcrystalline wax (E 905 as a food additive with the currently authorised uses would not be of safety concern.

  20. 均质纤维素膜的制备及其正渗透性能研究%Preparation and performance of homogeneous cellulose forward osmosis membrane

    Institute of Scientific and Technical Information of China (English)

    张兵涛; 张林; 黄和; 侯立安

    2014-01-01

    以纤维素(cellulose)为膜材料,离子液体1-乙基-3甲基咪唑醋酸盐(EMIMAc)为溶剂,水为非溶剂,无纺布作为支撑层,通过相转化法制备了纤维素均质膜。采用红外、X-射线衍射和扫描电子显微镜表征了膜的结构及形貌,考察了该膜的正渗透性能。结果表明:纤维素溶解再生过程中没有发生化学变化,但晶型发生了转变;当原料液为0.6 mol/L的氯化钠水溶液,汲取液为特制的营养液时,所制备的正渗透膜的水通量为3.534 L/(m2· h),截盐率达到99%以上。%The-nonporous-homogeneous-cellulose-membrane-for-forward-osmosis-was-pre-pared-via-phase-inversion-method-using-ionic-liquid-1-ethyl-3-methyl-imidazolium-acetate-(EMI-MAc)-as-solvent,water-as-nonsolvent-on-a-non-woven-fabric-substrate.-The-characterizations-of-Fourier-transform-infrared-(FTIR)-and-X-ray-diffraction-(XRD)-spectroscopies-showed-that-no-obvious-change-occurred-in-the-chemical-structure-of-cellulose-after-membrane-formation,but-the-crystallinity-had-a-certain-degree-of-decline.-The-cross-section-and-the-surface-morphologies-of-the-cellulose-forward-osmosis-membrane-were-analyzed-by-scanning-electron-microscopy-(SEM).-The-membrane-performance-were-investigated-by-measuring-water-flux-and-rejection-of-simulated-seawater.-The-water-flux-of-the-cellulose-forward-osmosis-membrane,which-the-cellu-lose-concentration-is-8%(wt)-in-casting-solution,was-3.534-L/m2-·-h-and-the-rejection-for-NaCl-was-more-than-99%,using-0.6-mol/L-NaCl-solution-as-the-feed-solution-and-lab-made-nutrient-solution-as-the-draw-solution.

  1. SYNTHESIS AND CHARACTERIZATION OF THE LAMELLAR MICROCRYSTALLINE ZINC PHOSPHATE α-Zn3 (PO4)2·4H2O

    Institute of Scientific and Technical Information of China (English)

    Yuan Aiqun; Bai Lijuan; Ma Shaomei; Tong Zhangfa

    2006-01-01

    Objective To study the structural and anticorrosive property of microcrystalline α-Zn3 (PO4)2 ·4H2O. Methods Zinc phosphate was prepared from zinc acetate and orthophosphate acid in aqueous solution.Structural characteristics of products were investigated by XRD, RAMAN, FTIR, TG-DTA, SEM, surface area,particle size distribution, and density measurements. Results The title compound, a highly crystalline, micronized (A), c0 =5. 0304(A), V=975.86 (A)3. Its specific area is 0. 701 m2/g, density 3. 1612 g/m3 , and average size 4.75μm . Conclusion Comparing with commercial Zinc phosphate, the synthesized iamellar microcrystalline zinc phosphate had excellent anticorrosive property and dispersibility.

  2. 尾矿粉/秸秆纤维素/环氧树脂复合材料制备及性能研究%Research on Preparation and Properties of Tailings Powder/Straw Cellulose/Epoxy Resin Composites

    Institute of Scientific and Technical Information of China (English)

    侯桂香; 于守武; 李婷婷; 王浩然; 桑晓明

    2012-01-01

    采用甲苯和乙醇萃取,碱液、过氧化氢溶液浸泡提取的秸秆纤维素和用硅烷偶联剂KH560表面改性处理的尾矿粉,作为添加剂加入到环氧树脂(E-44)固化体系中,制备尾矿粉/秸秆纤维素/环氧树脂复合材料;并对复合材料的力学性能、热性能、结构与形态进行测试与表征.结果表明:纤维素的(-OH)结构已经部分参与到环氧树脂的固化反应中.复合材料的冲击强度、热稳定性随秸秆纤维素和尾矿粉的加入而增加,冲击强度最高的配方为纤维素质量分数为5%,尾矿粉质量分数为10%,冲击强度为1.096 kJ/m2;拉伸强度则随尾矿粉的加入而下降.SEM分析表明:秸秆纤维素及尾矿粉的存在使得断面呈现出韧窝结构,复合材料体系产生相界面效应.%In this paper,straw cellulose was abstracted by extracting with toluene and ethanol as solvent,and then dipping in alkali and hydrogen peroxide solution.Tailings powder was deal with by silane coupling agent(KH560) and was added into epoxy resin E-44.Tailings powder/straw fiber/epoxy resin composites were prepared.The mechanical properties,thermal stability,structure and morphology of the composites were investigated and characterized.FTIR results showed that the reaction of (-OH) of the cellulose occurred in the process of curing reaction of the epoxy resin.The impact strength and thermal stability of the composite increased with the addition of straw cellulose and tailings powder.The results indicated that when the mass fraction of cellulose was 5% of the straw cellulose,and tailings was 10% ,impact strength was 1.096 kJ/m2,and the impact performance was the best.Tensile strength decreased with the addition of tailing powder.SEM showed that straw cellulose and tailings powder increased the phase interface effect of the composite and the cross section had the distribution of dimple type structure.

  3. Reinforcement of all-cellulose nanocomposite films using native cellulose nanofibrils.

    Science.gov (United States)

    Zhao, Jiangqi; He, Xu; Wang, Yaru; Zhang, Wei; Zhang, Xinxing; Zhang, Xiaodan; Deng, Yulin; Lu, Canhui

    2014-04-15

    All-cellulose nanocomposite films were prepared using native cellulose nanofibrils (CNFs) as fillers and lithium chloride/N,N-dimethylacetamide (LiCl/DMAc) dissolved regenerated cellulose as the matrix. The CNFs, with diameters in the range of 15-40 nm were obtained by combined physical methods of ultrasonic treatment and high shear homogenization. The morphology, structure, and properties of the nanocomposite films were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), optical transmittance, thermal gravimetric analysis (TGA), and mechanical testing. The nanocomposite films exhibited good optical transparency, thermal stability, and remarkably enhanced mechanical properties compared to the regenerated cellulose matrix. By varying the CNFs content, the tensile strength of the nanocomposite films increased from 61.56 MPa to 99.92 MPa and the Young's modulus increased from 0.76 GPa to 4.16 GPa. This work provided a promising pathway for manufacturing high performance and environmental-friendly all-cellulose nanocomposites.

  4. Cellulose Anionic Hydrogels Based on Cellulose Nanofibers As Natural Stimulants for Seed Germination and Seedling Growth.

    Science.gov (United States)

    Zhang, Hao; Yang, Minmin; Luan, Qian; Tang, Hu; Huang, Fenghong; Xiang, Xia; Yang, Chen; Bao, Yuping

    2017-05-17

    Cellulose anionic hydrogels were successfully prepared by dissolving TEMPO-oxidized cellulose nanofibers in NaOH/urea aqueous solution and being cross-linked with epichlorohydrin. The hydrogels exhibited microporous structure and high hydrophilicity, which contribute to the excellent water absorption property. The growth indexes, including the germination rate, root length, shoot length, fresh weight, and dry weight of the seedlings, were investigated. The results showed that cellulose anionic hydrogels with suitable carboxylate contents as plant growth regulators could be beneficial for seed germination and growth. Moreover, they presented preferable antifungal activity during the breeding and growth of the sesame seed breeding. Thus, the cellulose anionic hydrogels with suitable carboxylate contents could be applied as soilless culture mediums for plant growth. This research provided a simple and effective method for the fabrication of cellulose anionic hydrogel and evaluated its application in agriculture.

  5. Cellulose Solubility in Ionic Liquid Mixtures: Temperature, Cosolvent, and Antisolvent Effects.

    Science.gov (United States)

    Minnick, David L; Flores, Raul A; DeStefano, Matthew R; Scurto, Aaron M

    2016-08-18

    Select ionic liquids (ILs) dissolve significant quantities of cellulose through disruption and solvation of inter- and intramolecular hydrogen bonds. In this study, thermodynamic solid-liquid equilibrium was measured with microcrystalline cellulose in a model IL, 1-ethyl-3-methylimidazolium diethyl phosphate ([EMIm][DEP]) and mixtures with protic antisolvents and aprotic cosolvents between 40 and 120 °C. The solubility of cellulose in pure [EMIm][DEP] exhibits an asymptotic maximum of approximately 20 mass % above 100 °C. Solubility studies conducted on antisolvent mixtures with [EMIm][DEP] and [BMIm][Cl] indicate that protic solvents, ethanol, methanol, and water, significantly reduce the cellulose capacity of IL mixtures by 38-100% even at small antisolvent loadings (<5 mass %). Alternatively, IL-aprotic cosolvent (dimethyl sulfoxide, dimethylformamide, and 1,3-dimethyl-2-imidazolidinone) mixtures at mass ratios up to 1:1 enhance cellulose dissolution by 20-60% compared to pure [EMIm][DEP] at select temperatures. Interactions between the IL and molecular solvents were investigated by Kamlet-Taft solvatochromic analysis, FTIR, and NMR spectroscopy. The results indicate that preferential solvation of the IL cation and anion by co- and antisolvents impact the ability of IL ions to interact with cellulose thus affecting the cellulose dissolution capacity of IL-solvent mixtures.

  6. Solid acid-catalyzed cellulose hydrolysis monitored by in situ ATR-IR spectroscopy.

    Science.gov (United States)

    Zakzeski, Joseph; Grisel, Ruud J H; Smit, Arjan T; Weckhuysen, Bert M

    2012-02-13

    The solid acid-catalyzed hydrolysis of cellulose was studied under elevated temperatures and autogenous pressures using in situ ATR-IR spectroscopy. Standards of cellulose and pure reaction products, which include glucose, fructose, hydroxymethylfurfural (HMF), levulinic acid (LA), formic acid, and other compounds, were measured in water under ambient and elevated temperatures. A combination of spectroscopic and HPLC analysis revealed that the cellulose hydrolysis proceeds first through the disruption of the glycosidic linkages of cellulose to form smaller cellulose molecules, which are readily observed by their distinctive C-O vibrational stretches. The continued disruption of the linkages in these oligomers eventually results in the formation and accumulation of monomeric glucose. The solid-acid catalyst accelerated the isomerization of glucose to fructose, which then rapidly reacted under hydrothermal conditions to form degradation products, which included HMF, LA, formic acid, and acetic acid. The formation of these species could be suppressed by decreasing the residence time of glucose in the reactor, reaction temperature, and contact with the metal reactor. The hydrolysis of regenerated cellulose proceeded faster and under milder conditions than microcrystalline cellulose, which resulted in increased glucose yield and selectivity. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Electrically conductive cellulose composite

    Science.gov (United States)

    Evans, Barbara R.; O'Neill, Hugh M.; Woodward, Jonathan

    2010-05-04

    An electrically conductive cellulose composite includes a cellulose matrix and an electrically conductive carbonaceous material incorporated into the cellulose matrix. The electrical conductivity of the cellulose composite is at least 10 .mu.S/cm at 25.degree. C. The composite can be made by incorporating the electrically conductive carbonaceous material into a culture medium with a cellulose-producing organism, such as Gluconoacetobacter hansenii. The composites can be used to form electrodes, such as for use in membrane electrode assemblies for fuel cells.

  8. Preparation and Absorption Properties of Cellulose Modified by Graphene Oxide%氧化石墨烯改性纤维素的制备及对Cu2+吸附性能的研究

    Institute of Scientific and Technical Information of China (English)

    唐杰; 邓继勇

    2015-01-01

    Graphite oxide was prepared by Hummers method and exfoliated into graphene oxide sheets through ultrasonic process .Then the graphene oxide sheets with alkali cellulose was blended to prepare the strong absorption composite material . Their structures and properties were characterized by infrared spectroscopy (IR) ,Zeta potential ,X -Ray Diffraction (XRD )and other analytical methods . This article discussed the absorbent input , pH value of solution , absorption time , absorption temperature and other factors which effect the performance of the adsorption of heavy metals .The result showed that the absorption of composite material had increments of 97 .41% when compared to the cellulose .%通过改进的Hummers法制备氧化石墨,进而超声剥离制备氧化石墨烯;再将氧化石墨烯悬浮液和碱性纤维素溶液混合制备强吸附性复合材料。使用红外光谱(IR)、Zeta电位仪、X射线衍射(XRD )等测试仪器对材料的结构与性能进行表征。探讨了吸附剂用量、溶液p H、吸附时间和吸附温度等影响因素对C u2+吸附性能的影响。结果表明:复合材料吸附能力较纤维素提高了97.41%。

  9. Magnetic alignment and patterning of cellulose fibers

    Directory of Open Access Journals (Sweden)

    Fumiko Kimura and Tsunehisa Kimura

    2008-01-01

    Full Text Available The alignment and patterning of cellulose fibers under magnetic fields are reported. Static and rotating magnetic fields were used to align cellulose fibers with sizes ranging from millimeter to nanometer sizes. Cellulose fibers of the millimeter order, which were prepared for papermaking, and much smaller fibers with micrometer to nanometer sizes prepared by the acid hydrolysis of larger ones underwent magnetic alignment. Under a rotating field, a uniaxial alignment of fibers was achieved. The alignment was successfully fixed by the photopolymerization of a UV-curable resin precursor used as matrix. A monodomain chiral nematic film was prepared from an aqueous suspension of nanofibers. Using a field modulator inserted in a homogeneous magnetic field, simultaneous alignment and patterning were achieved

  10. Magnetic alignment and patterning of cellulose fibers

    Energy Technology Data Exchange (ETDEWEB)

    Kimura, Fumiko; Kimura, Tsunehisa [Division of Forest and Biomaterials Science, Graduate School of Agriculture, Kyoto University, Kitashirakawa, Sakyo-ku, Kyoto 606-8502 (Japan)], E-mail: tkimura@kais.kyoto-u.ac.jp

    2008-04-01

    The alignment and patterning of cellulose fibers under magnetic fields are reported. Static and rotating magnetic fields were used to align cellulose fibers with sizes ranging from millimeter to nanometer sizes. Cellulose fibers of the millimeter order, which were prepared for papermaking, and much smaller fibers with micrometer to nanometer sizes prepared by the acid hydrolysis of larger ones underwent magnetic alignment. Under a rotating field, a uniaxial alignment of fibers was achieved. The alignment was successfully fixed by the photopolymerization of a UV-curable resin precursor used as matrix. A monodomain chiral nematic film was prepared from an aqueous suspension of nanofibers. Using a field modulator inserted in a homogeneous magnetic field, simultaneous alignment and patterning were achieved.

  11. 再生纤维素/胶原蛋白复合伤口敷料的制备及其性能评价*%The preparation of regenerated cellulose/collagen composite wound dressing and its performance evaluation

    Institute of Scientific and Technical Information of China (English)

    陆金婷; 程咏梅; 赵朋; 吕国忠; 陈敬华

    2014-01-01

    In this study,an approach to prepare regenerated cellulose/collagen composite dressing was pro-posed.Firstly,regenerated cellulose membrane was oxidized by periodate oxidation for the preparation of 2,3-dialdehyde cellulose (DARC,the dialdehyde content was 6 .1 1%),and then it was reacted with collagen to ob-tain the target DARC-Col composite dressing by Schiff base reaction.The scanning electron microscopy re-vealed that DARC-Col composite dressing exhibited the refined network structures.In addition,the composite dressing showed novel mechanical properties (the strain was 78.09 MPa,the stress was 9.59%),good equilib-rium-swelling ratio (182%),good air permeability (703.72 g/m2 ·d)and excellent water retaining property (20%).Furthermore,the test of NIH3T3 mice fibroblast cells indicated that DARC-Col could promote cell growth and proliferation.The DARC-Col composite dressing showed great potential as ideal wound dressing for the wound repair application.%用高碘酸钠将再生纤维素膜(RC)部分氧化,得到具有醛基的2,3-二醛纤维素膜(DARC,醛基含量为6.11%),再通过席夫碱反应将胶原蛋白固定到DARC膜上,制备得到DARC-Col复合敷料。SEM结果显示DARC-Col复合敷料具有多孔网络结构。该材料具有良好的机械性能(拉伸强度78.09 MPa,断裂伸长率9.59%),溶胀性能(182%),透湿性(703.72 g/m2·d)和保水性(20%)。NIH-3T3小鼠成纤维细胞实验结果表明,该材料能有效促进细胞的生长和增殖,具有作为理想的伤口敷料应用于伤口修复治疗的巨大潜能。

  12. Synthesis and characterization of polyvinyl alcohol/cellulose cryogels and their testing as carriers for a bioactive component

    Energy Technology Data Exchange (ETDEWEB)

    Paduraru, Oana Maria; Ciolacu, Diana; Darie, Raluca Nicoleta; Vasile, Cornelia, E-mail: cvasile@icmpp.ro

    2012-12-01

    Novel physically cross-linked cryogels containing polyvinyl alcohol (PVA) and various amounts of microcrystalline cellulose were obtained by freezing/thawing technique. The main goal of this study was to improve the properties and the performances of the pure PVA cryogels. The morphological aspects of the cryogels were studied by scanning electron microscopy (SEM). The Fourier transform infrared spectroscopy (FT-IR) was used to reveal the presence of the interactions between the two polymers. Changes in crystallinity of the samples were confirmed by X-ray diffraction (XRD) and by FT-IR spectroscopy. The modification of the thermal behavior induced by cellulose was studied by thermogravimetry. Rheological analysis revealed higher values of storage modulus (G Prime ) for the cryogels containing higher amounts of cellulose. The degree and rate of swelling were controlled by the presence of the natural polymer in the network. The potential application as bioactive compound carriers was tested, using vanillin as an active agent. Highlights: Black-Right-Pointing-Pointer Novel PVA/microcrystalline cellulose cryogels were obtained by freezing/thawing. Black-Right-Pointing-Pointer The main advantage of this technique is that no chemical crosslinker is being used. Black-Right-Pointing-Pointer The presence of cellulose improves the swelling properties and the cryogels' strength. Black-Right-Pointing-Pointer The potential application as carriers for bioactive components was tested.

  13. Percutaneous microcrystalline chitosan application for sealing arterial puncture sites.

    Science.gov (United States)

    Hoekstra, A; Struszczyk, H; Kivekäs, O

    1998-08-01

    Arterial catheterization is one of the most frequently performed inpatient diagnostic and therapeutic procedures in the development countries. Complications may occur after any catheterization from inadequate hemostasis, particularly in the setting of aggressive anticoagulation. This study suggests that microcrystalline chitosan (MCCh) sealant installation via an arterial sheath at the completion of catheterization may improve hemostasis. Results using MCCh in eight heparinized dogs documented significant reductions in manual compression time (P = 0.016) of the artery after withdrawal of both the sheath introducer and catheter. Comparative results were found in rats, wherein a created wound in the aorta could be sealed relatively quickly and easily. The biodegradability, optimalization, and a better pharmaceutical formulation of this potential hemostatic agent require further studies.

  14. Device simulation and modeling of microcrystalline silicon solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Takakura, H.; Hamakawa, Y. [Ritsumeikan Univ., Shiga (Japan). Dept. of Photonics

    2002-10-01

    Device modeling for p-i-n junction basis thin film microcrystalline Si solar cells has been examined with a simple model of columnar grain structure utilizing two-dimensional device simulator. The simulation results of solar cell characteristics show that open-circuit voltage (V{sub oc}) and fill factor considerably depend on structural parameters such as grain size and acceptor doping in intrinsic layer, while short-circuit current density (J{sub sc}) is comparatively stable by built-in electric field in the i-layer. It is also found that conversion efficiency of more than 16% could be expected with 1 {sup {mu}}m grain size and well-passivated condition with 10 {sup {mu}}m thick i-layer and optical confinement. (Author)

  15. Synthesis and characterization of superabsorbent polymer prepared by radiation-induced graft copolymerization of acrylamide onto carboxymethyl cellulose for controlled release of agrochemicals

    Science.gov (United States)

    Hemvichian, Kasinee; Chanthawong, Auraruk; Suwanmala, Phiriyatorn

    2014-10-01

    Superabsorbent polymer (SAP) was synthesized by radiation-induced grafting of acrylamide (AM) onto carboxymethyl cellulose (CMC) in the presence of a crosslinking agent, N,N‧-methylenebisacrylamide (MBA). The effects of various parameters, such as dose, the amount of CMC, AM, MBA and ionic strength on the swelling ratio were investigated. In order to evaluate its controlled release potential, SAP was loaded with potassium nitrate (KNO3) as an agrochemical model and its potential for controlled release of KNO3 was studied. The amount of released KNO3 was analyzed by an inductively coupled plasma mass spectrometry (ICP-MS). The results from controlled release experiment agreed very well with the results from swelling experiment. The synthesized SAP was characterized by Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). The obtained SAP exhibited a swelling ratio of 190 g/g of dry gel.

  16. Posidonia oceanica as a Renewable Lignocellulosic Biomass for the Synthesis of Cellulose Acetate and Glycidyl Methacrylate Grafted Cellulose

    Directory of Open Access Journals (Sweden)

    Elena Vismara

    2013-05-01

    Full Text Available High-grade cellulose (97% α-cellulose content of 48% crystallinity index was extracted from the renewable marine biomass waste Posidonia oceanica using H2O2 and organic peracids following an environmentally friendly and chlorine-free process. This cellulose appeared as a new high-grade cellulose of waste origin quite similar to the high-grade cellulose extracted from more noble starting materials like wood and cotton linters. The benefits of α-cellulose recovery from P. oceanica were enhanced by its transformation into cellulose acetate CA and cellulose derivative GMA-C. Fully acetylated CA was prepared by conventional acetylation method and easily transformed into a transparent film. GMA-C with a molar substitution (MS of 0.72 was produced by quenching Fenton’s reagent (H2O2/FeSO4 generated cellulose radicals with GMA. GMA grafting endowed high-grade cellulose from Posidonia with adsorption capability. GMA-C removes β-naphthol from water with an efficiency of 47%, as measured by UV-Vis spectroscopy. After hydrolysis of the glycidyl group to glycerol group, the modified GMA-C was able to remove p-nitrophenol from water with an efficiency of 92%, as measured by UV-Vis spectroscopy. α-cellulose and GMA-Cs from Posidonia waste can be considered as new materials of potential industrial and environmental interest.

  17. Efficient cellulose solvent: quaternary ammonium chlorides.

    Science.gov (United States)

    Kostag, Marc; Liebert, Tim; El Seoud, Omar A; Heinze, Thomas

    2013-10-01

    Pure quaternary tetraalkylammonium chlorides with one long alkyl chain dissolved in various organic solvents constitute a new class of cellulose solvents. The electrolytes are prepared in high yields and purity by Menshutkin quaternization, an inexpensive and easy synthesis route. The pure molten tetraalkylammonium chlorides dissolve up to 15 wt% of cellulose. Cosolvents, including N,N-dimethylacetamide (DMA), may be added in large excess, leading to a system of decreased viscosity. Contrary to the well-established solvent DMA/LiCl, cellulose dissolves in DMA/quaternary ammonium chlorides without any pretreatment. Thus, the use of the new solvent avoids some disadvantages of DMA/LiCl and ionic liquids, the most extensively employed solvents for homogeneous cellulose chemistry.

  18. Influence of substitution on the rheological properties and gelation of hydroxyethyl cellulose solution in NaOH-water solvent.

    Science.gov (United States)

    Wang, Wencong; Li, Faxue; Yu, Jianyong; Navard, Patrick; Budtova, Tatiana

    2015-06-25

    The rheological properties of hydroxyethyl cellulose (HEC) with a low molar substitution (MS) dissolved in 8wt% NaOH-water were studied as a function of solution temperature, polymer concentration and molar substitution. Special attention was paid to gelation kinetics. Similar to cellulose dissolved in alkali or ionic liquids, the intrinsic viscosity of HEC decreased with temperature increase, indicating a decrease of solvent thermodynamic quality. The gelation time of HEC solutions decreased exponentially with temperature but the kinetics is much slower than the gelation of microcrystalline cellulose solutions in the same solvent. Higher molar substitution leads to slower gelation. The small amount of introduced hydroxyethyl groups prevented cellulose aggregation thus increasing solution stability.

  19. 新型键合纤维素手性固定相的制备及其拆分性能评价%Preparation of a new immobilized cellulose-based chiral stationary phase and its enantioseparation behaviors

    Institute of Scientific and Technical Information of China (English)

    涂鸿盛; 范军; 谭艺; 林纯; 华江颖; 章伟光

    2014-01-01

    The immobilized polysaccharide-based chiral stationary phase has attracted consid-erable attention over the past decades due to its high chemical stability,good solvent resist-ance,great enantioseparation ability,etc. In this study,a new immobilized cellulose chiral sta-tionary phase(denoted as ImCel)was prepared through the Staudinger reaction of 6-azido-6-deoxy-cellulose-3,5-dichlorophenylcarbamate and aminopropyl silica gel. The enantioseparation performance of the Imcellfor 20 pairs of chiral analytes and the effect of non-standard solvents have been investigated by high performance liquid chromatography. Baseline separations of 17 pairs of enantiomers were achieved on the ImCel. The separation ability of the Imcellin the nor-mal mode was much better than in reversed mode. In addition,the Imcellshowed good chemi-cal stability in the non-standard mobile phase due to the covalent bonds between the cellulose chiral selectors and silica support. Moreover,it exhibited complementarity with another immo-bilized-cellulose chiral stationary phase containing 3,5-dimethylphenylcarbamate groups for the separation of a series of 9-fluorenylmethyloxycarbonyl ( fmoc )-derived amino acids. The reversal of enantiomer elution order induced by the difference of the substituents in chiral sta-tionary phase was observed under the same chromatographic conditions. In brief,a new immo-bilized cellulose chiral stationary phase with high stability and good separation performance was developed in this work.%键合型多糖手性固定相因具有化学稳定性高和溶剂耐受性好的特点而受到研究者的极大关注。采用施陶丁格( Staudinger)反应将6-叠氮-6-脱氧纤维素-3,5-二氯苯基氨基甲酸酯键合到氨丙基硅胶上得到一种新的键合型手性固定相( ImCel),研究了其手性分离性能,并探讨了非常规流动相(如氯仿、四氢呋喃等)的影响。结果表明,在20对手性化合物中,17对在合适的流动

  20. Investigation of carrier density and mobility in microcrystalline silicon alloys using Hall effect and thermopower measurements; Untersuchung der Ladungstraegerkonzentration und -beweglichkeit in mikrokristallinen Siliziumlegierungen mit Hall-Effekt und Thermokraft

    Energy Technology Data Exchange (ETDEWEB)

    Sellmer, Christian

    2012-08-31

    The electronic properties of amorphous and microcrystalline silicon layers in thin-film solar cells significantly affect the efficiency of solar cells. An important property of the individual layer is the electronic transport, which is described by the variables conductivity, photoconductivity, mobility, and carrier concentration. In the past, individual characterization methods were typically used to determine the electronic properties. Using the combination of Hall effect, conductivity, and thermoelectric power measurements additional variables can be derived, such as the effective density of states at the valence and conduction band edge, making a more detailed description of the material possible. To systematically study the electronic properties - in particular carrier mobility and carrier concentration - various series of silicon films are prepared for this work including microcrystalline silicon layers of different doping and crystallinity and a series of silicon films where the Fermi level is moved by irradiation with high energy electrons on one and the same sample. The results show that the transition from amorphous to microcrystalline transport is relatively abrupt. If the electron transport takes place in only amorphous regions, it is marked by the sign anomaly of the Hall effect. If a continuous crystalline path exists, the electronic properties are dominated by the crystalline volume fraction. The results of the measurements of silicon layers are compared with those of microcrystalline silicon carbide samples. Silicon carbide is especially interesting for future applications in thin-film solar cells due to high transparency and high conductivity. It is shown that the effective density of states at the valence and conduction band edge as a function of temperature in p- and n-type microcrystalline silicon and silicon carbide samples largely coincide with those of crystalline silicon or silicon carbide. A square root shaped profile of the density of

  1. Preparation of Glyoxal from Cellulose by Plasma Electrolysis%等离子体电解纤维素制备乙二醛

    Institute of Scientific and Technical Information of China (English)

    李秀帆; 陈砺; 严宗诚

    2014-01-01

    Using cellulose as the raw material, effects of three kinds of metal ions (K+, Ca2+, Fe2+) on the production of glyoxal was investigated with plasma electrolysis. Results showed that the presence of metal ions (K+, Ca2+, Fe2+) could improve the production of glyoxal significantly. The order of effects of the three kinds of metal ions from strong to weak was Fe2+>K+>Ca2+. With the increase of conductivity, the concentration of glyoxal was increased at first and then decreased. The concentration of glyoxal reached a maximum value when the conductivity was 10~15 mS/cm. The concentration of glyoxal was increased first and then decreased with the prolonging reaction and reached a maximum value at 15 min. The results of X-ray diffraction and fourier transform infrared spectroscopy showed that plasma electrolysis could break down the crystallized zone and hydrogen bonding of cellulose.%以纤维素为原料,在等离子体电解条件下,研究了K+、Ca2+、Fe2+3种金属离子对纤维素降解制备乙二醛的影响。结果表明, K+、Ca2+、Fe2+3种金属离子对纤维素降解有明显的催化作用,其催化作用大小依次为Fe2+、K+、Ca2+。乙二醛的浓度随着电导率的增大,先升高后降低;电导率为10~15 mS∕cm时,乙二醛浓度达到最大值。乙二醛的浓度随着反应时间的延长,先升高后降低;在15 min时,乙二醛浓度达到最大值。 X射线衍射结果显示,等离子体电解破坏了纤维素结晶区结构,结晶度显著下降;傅里叶红外变换光谱结果表明,等离子产生的活性粒子对分子间和分子内氢键有解缔作用,使其强度降低。

  2. Immobilization of Glucose Oxidase on Cellulose/Cellulose Acetate Membrane and its Detection by Scanning Electrochemical Microscope (SECM)

    Institute of Scientific and Technical Information of China (English)

    Jin Sheng ZHAO; Zhen Yu YANG; Yi He ZHANG; Zheng Yu YANG

    2004-01-01

    Cellulose/cellulose acetate membranes were prepared and functionalized by introducing amino group on it, and then immobilized the glucose oxidase (Gox) on the functionalizd membrane. SECM was applied for the detection of enzyme activity immobilized on the membrane. Immobilized biomolecules on such membranes was combined with analysis apparatus and can be used in bioassays.

  3. Microcrystalline sodium tungsten bronze nanowire bundles as efficient visible light-responsive photocatalysts.

    Science.gov (United States)

    Wang, Lei; Zhan, Jinhua; Fan, Weiliu; Cui, Guanwei; Sun, Honggang; Zhuo, Linhai; Zhao, Xian; Tang, Bo

    2010-12-14

    Microcrystalline sodium tungsten bronze nanowire bundles were obtained via a facile hydrothermal synthesis, and were applied in water purification as visible-light-driven photocatalysts for the first time.

  4. 玉米秸秆微晶纤维素/聚乳酸复合膜的制备与性能%Preparation and properties of corn stalks cellulose microcrystal reinforced poly(lactic acid) composite film

    Institute of Scientific and Technical Information of China (English)

    李春光; 徐鹏飞; 李云霞; 王彦秋; 林鹏; 张锐

    2011-01-01

    The biodegradable composite films were prepared from corn stalks cellulose microcrystal(CSCMC) as the filler and poly(lactic acid)(PLA) as the polymeric matrix.The crystallinity,the tensile properties and the thermal properties of the composite flim were tested.The results show that the tensile properties and the thermal properties of the CSCMC/PLA composite were improved by the addition of corn stalks cellulose microcrystal.When the mass fraction of CSCMC is 10%,the initial decomposition temperature increases by 34.38℃,the tensile strength increases by 58.3% and the elongation at break increases by 31.1% compared to that of the pure PLA.%采用玉米秸秆微晶纤维素(CSCMC)作为增强材料,生物可降解材料聚乳酸(PLA)作为基体,制备了CSCMC/PLA复合膜材料,并对复合膜的结晶度、热稳定性能、力学性能进行了测试。结果表明,复合膜材料的热稳定性能和力学性能优于纯聚乳酸膜。当CSCMC的质量分数为10%时,复合膜的热稳定性能和力学性能达到最佳,与纯PLA膜相比,起始分解温度提高了34.38℃,拉伸强度提高了58.3%,断裂伸长率提高了31.1%。

  5. Investigation of the factors influencing the preparation process of cellulose triacetate forward osmosis membrane%三醋酸纤维素正渗透膜制备过程中影响因素的研究

    Institute of Scientific and Technical Information of China (English)

    刘蕾蕾; 王铎; 汪锰; 高从堦

    2011-01-01

    Cellulose triacetate forward osmosis membrane was prepared by phase inversion method. The polymer solution consisted of cellulose triacetate as the membrane material, 1, 4-dioxane and acetone as solvent, and lactic acid as additives. The effects of support materials, solvent evaporation time and the additive content on the membrane performance were investigated. 0. 1 mol/L NaCl was used as the feed solution and 4 mol/L glucose was used as the draw solution. The water flux was between 6 and 7 L/(m2 · h) and the rejection for NaCl was above 95%.%以三醋酸纤维素为膜材料,以1,4-二氧六环和丙酮为溶剂,乳酸为添加剂.采用相转化法制备三醋酸纤维素正渗透膜.研究了不同支撑材料以及膜制备过程中溶剂挥发时间和添加剂的含量对正渗透膜性能的影响.结果表明,在原料液为0.1 mol/L NaCl,汲取液为4 mol/L葡萄糖,原料液面向分离层,室温的测试条件下,采用180目(80 μm)的筛网为支撑体材料,挥发时间为180 s,乳酸含量为6.6%所制备的三醋酸纤维素正渗透膜的水通量为6~7 L/(m2·h),NaCl截留率在95%以上.

  6. ECOLOGY SAFE METHOD OF OBTAINING FROM FIR-WOOD THE CELLULOSIC PRODUCT WITH HIGH CONTENT OF ALFA-CELLULOSE

    OpenAIRE

    Владимир Александрович Левданский; Александр Владимирович Левданский; Борис Николаевич Кузнецов

    2014-01-01

    The «green» method of obtaining from fir-wood the cellulosic product with high content of alpha-cellulose was developed. It consists of the stage of wood delignification by hydrogen peroxide in the medium «acetic acid – water – sulfuric acid catalyst» and of the stage of alkaline treatment by NaOH. Preparation conditions were selected which allow to obtain with an acceptable yield (30–31% mas.) the cellulosic product containing 97,3–98,0% mas. of alpha-cellulose.

  7. PREPARATION AND MECHANICAL PROPERTIES OF LAYERED BC NANO-CELLULOSE MEMBRANE/PVA COMPOSITE HYDROGELS%层状纳米纤维素膜/PVA复合水凝胶的制备与力学性能研究

    Institute of Scientific and Technical Information of China (English)

    谭珏; 郑裕东; 彭江; 吴健; 高爽; 田茹; 陈红谚

    2012-01-01

    采用叠层复合与物理相分离的方法制备了层状纳米细菌纤维素(BC)膜/聚乙烯醇( PVA)复合水凝胶.研究了聚乙烯醇的质量百分数、BC膜的复合层数以及制备条件对复合水凝胶力学性能的影响;通过扫描电镜( SEM)观察比较了复合水凝胶中BC膜层与PVA界面结合情况.结果表明,复合水凝胶的力学性能与PVA的质量百分数和BC膜含水量、BC膜的层数以及制备条件有关.PVA质量百分数较高,流动性变差,界面结合差,导致复合水凝胶力学性能下降.当PVA质量百分数为15%、BC膜的层数为2层时,在相同的温度和条件下制备的复合水凝胶界面黏结良好,弹性模量、抗拉强度为7.82、1.74 MPa.%Bacterial nano-cellulose ( BC ) membranes of high purity, ultrafine network architecture and excellent biocompatibility were used to reinforce the poly ( vinyl alcohol) ( PVA ) hydrogels, which were prepared by physical method of freezing and thawing. The mechanical properties of the BC/PVA composite hydrogels were investigated,the mass percent of PVA,the number of BC layers and some other conditions like pre-treatment method of BC membranes were considered in the preparation process. The mechanical properties of the BC/PVA composite hydrogels were tested by tensile testing machine, the fracture surface of the composite hydrogels and the bonding situation between the BC nano-cellulose membrane and the PVA hydrogel were characterized by the scanning electron microscopy (SEM).The results show that the BC/PVA composite hydrogels have excellent mechanical properties, the tensile strength of the composite hydrogel reaches to 1. 74 Mpa,and the modulus reaches to 7.82 Mpa,when the BC/PVA composite hydrogels are constituted by 15 wt% PVA and two layers of BC membranes. The SEM images show that the interface of the prepared composite hydrogels exhibits excellent bonding.

  8. Structure and transformation of tactoids in cellulose nanocrystal suspensions

    Science.gov (United States)

    Wang, Pei-Xi; Hamad, Wadood Y.; MacLachlan, Mark J.

    2016-05-01

    Cellulose nanocrystals obtained from natural sources are of great interest for many applications. In water, cellulose nanocrystals form a liquid crystalline phase whose hierarchical structure is retained in solid films after drying. Although tactoids, one of the most primitive components of liquid crystals, are thought to have a significant role in the evolution of this phase, they have evaded structural study of their internal organization. Here we report the capture of cellulose nanocrystal tactoids in a polymer matrix. This method allows us to visualize, for the first time, the arrangement of cellulose nanocrystals within individual tactoids by electron microscopy. Furthermore, we can follow the structural evolution of the liquid crystalline phase from tactoids to iridescent-layered films. Our insights into the early nucleation events of cellulose nanocrystals give important information about the growth of cholesteric liquid crystalline phases, especially for cellulose nanocrystals, and are crucial for preparing photonics-quality films.

  9. Green thermal-assisted synthesis and characterization of novel cellulose-Mg(OH)2 nanocomposite in PEG/NaOH solvent.

    Science.gov (United States)

    Ponomarev, Nikolai; Repo, Eveliina; Srivastava, Varsha; Sillanpää, Mika

    2017-11-15

    Synthesis of nanocomposites was performed using microcrystalline cellulose (MCC), MgCl2 in PEG/NaOH solvent by a thermal-assisted method at different temperatures by varying time and the amount of MCC. Results of XRD, FTIR, and EDS mapping showed that the materials consisted of only cellulose (CL) and magnesium hydroxide (MH). According to FTIR and XRD, it was found that crystallinity of MH in cellulose nanocomposites is increased with temperature and heating time and decreased with increasing of cellulose amount. The PEG/NaOH solvent has a significant effect on cellulose and Mg(OH)2 morphology. BET and BJH results demonstrated the effects of temperature and cellulose amount on the pore size corresponding to mesoporous materials. TG and DTG analyses showed the increased thermal stability of cellulose nanocomposites with increasing temperature. TEM and SEM analyses showed an even distribution of MH nanostructures with various morphology in the cellulose matrix. The cellulose presented as the polymer matrix in the nanocomposites. It was supposed the possible interaction between cellulose and Mg(OH)2. The novel synthesis method used in this study is feasible, cost-efficient and environmentally friendly. Copyright © 2017 Elsevier Ltd. All rights reserved.

  10. Cellulose fibers extracted from rice and oat husks and their application in hydrogel.

    Science.gov (United States)

    Oliveira, Jean Paulo de; Bruni, Graziella Pinheiro; Lima, Karina Oliveira; Halal, Shanise Lisie Mello El; Rosa, Gabriela Silveira da; Dias, Alvaro Renato Guerra; Zavareze, Elessandra da Rosa

    2017-04-15

    The commercial cellulose fibers and cellulose fibers extracted from rice and oat husks were analyzed by chemical composition, morphology, functional groups, crystallinity and thermal properties. The cellulose fibers from rice and oat husks were used to produce hydrogels with poly (vinyl alcohol). The fibers presented different structural, crystallinity, and thermal properties, depending on the cellulose source. The hydrogel from rice cellulose fibers had a network structure with a similar agglomeration sponge, with more homogeneous pores compared to the hydrogel from oat cellulose fibers. The hydrogels prepared from the cellulose extracted from rice and oat husks showed water absorption capacity of 141.6-392.1% and high opacity. The highest water absorption capacity and maximum stress the compression were presented by rice cellulose hydrogel at 25°C. These results show that the use of agro-industrial residues is promising for the biomaterial field, especially in the preparation of hydrogels.

  11. Preparation and evaluation of gastroretentive floating tablets of Silymarin.

    Science.gov (United States)

    Garg, Rajeev; Gupta, Ghanshyam Das

    2009-06-01

    The present study performed by preparation and evaluation of floating tablets of Silymarin as model drug for prolongation of gastric residence time. Floating effervescent tablets were formulated by various materials like hydroxypropyl methylcellulose (HPMC) K 4M, K 15M, psyllium husk, swelling agent as crospovidone and microcrystalline cellulose and gas generating agent like sodium bicarbonate and citric acid and evaluated for floating properties, swelling characteristics and in vitro drug release studies. Floating noneffervescent tablets were prepared by polypropylene foam powder and different matrix forming polymers like HPMC K 4M, Carbopol 934P, xanthan gum and sodium alginate. In vitro drug release studies were performed and drug release kinetics evaluated using the linear regression method was found to follow both the Higuchi and the Korsemeyer and Peppas equation. The drug release mechanism was found fickian type in most of the formulations. The developed floating tablets of Silymarin may be used in clinic for prolonged drug release for at least 24 h, thereby improving the bioavailability and patient compliance.

  12. Crystallization of II-VI semiconductor compounds forming long microcrystalline linear assemblies

    Directory of Open Access Journals (Sweden)

    Marcelino Becerril

    2013-04-01

    Full Text Available In this work we report the formation of long microcrystalline linear self-assemblies observed during the thin film growth of several II-VI compounds. Polycrystalline CdTe, CdS, CdCO3, and nanocrystalline CdTe:Al thin films were prepared on glass substrates by different deposition techniques. In order to observe these crystalline formations in the polycrystalline materials, the thin film growth was suspended before the grains reached to form a continuous layer. The chains of semiconductor crystals were observed among many isolated and randomly distributed grains. Since CdTe, CdTe:Al, CdS and CdCO3 are not ferroelectric and/or ferromagnetic materials, the relevant problem would be to explain what is the mechanism through which the grains are held together to form linear chains. It is well known that some nanocrystalline materials form rods and wires by means of electrostatic forces. This occurs in polar semiconductors, where it is assumed that the attraction forces between surface polar faces of the small crystals are the responsible for the chains formation. Since there are not too many mechanisms responsible for the attraction we assume that a dipolar interaction is the force that originates the formation of chain-like grain clusters. The study of this property can be useful for the understanding of nucleation processes in the growth of semiconductor thin films.

  13. Applicability of low-melting-point microcrystalline wax to develop temperature-sensitive formulations.

    Science.gov (United States)

    Matsumoto, Kohei; Kimura, Shin-Ichiro; Iwao, Yasunori; Itai, Shigeru

    2017-10-30

    Low-melting-point substances are widely used to develop temperature-sensitive formulations. In this study, we focused on microcrystalline wax (MCW) as a low-melting-point substance. We evaluated the drug release behavior of wax matrix (WM) particles using various MCW under various temperature conditions. WM particles containing acetaminophen were prepared using a spray congealing technique. In the dissolution test at 37°C, WM particles containing low-melting-point MCWs whose melting was starting at approx. 40°C (Hi-Mic-1045 or 1070) released the drug initially followed by the release of only a small amount. On the other hand, in the dissolution test at 20 and 25°C for WM particles containing Hi-Mic-1045 and at 20, 25, and 30°C for that containing Hi-Mic-1070, both WM particles showed faster drug release than at 37°C. The characteristic drug release suppression of WM particles containing low-melting-point MCWs at 37°C was thought attributable to MCW melting, as evidenced by differential scanning calorimetry analysis and powder X-ray diffraction analysis. Taken together, low-melting-point MCWs may be applicable to develop implantable temperature-sensitive formulations that drug release is accelerated by cooling at administered site. Copyright © 2017 Elsevier B.V. All rights reserved.

  14. Direct observation and mechanism of increased emission sites in Fe-coated microcrystalline diamond films

    Energy Technology Data Exchange (ETDEWEB)

    Panda, Kalpataru; Sundaravel, B.; Panigrahi, B. K. [Materials Physics Division, Indira Gandhi Centre for Atomic Research, Kalpakkam 603 102 (India); Huang, Pin-Chang; Shih, Wen-Ching [Graduate Institute in Electro-Optical Engineering, Tatung University, Taipei 104, Taiwan (China); Chen, Huang-Chin; Lin, I-Nan [Department of Physics, Tamkang University, New-Taipei 251, Taiwan (China)

    2012-06-15

    The electron field emission (EFE) properties of microcrystalline diamond (MCD) films are significantly enhanced due to the Fe coating and post-annealing processes. The 900 Degree-Sign C post-annealed Fe coated diamond films exhibit the best EFE properties, with a turn on field (E{sub 0}) of 3.42 V/{mu}m and attain EFE current density (J{sub e}) of 170 {mu}A/cm{sup 2} at 7.5 V/{mu}m. Scanning tunnelling spectroscopy (STS) in current imaging tunnelling spectroscopy mode clearly shows the increased number density of emission sites in Fe-coated and post-annealed MCD films than the as-prepared ones. Emission is seen from the boundaries of the Fe (or Fe{sub 3}C) nanoparticles formed during the annealing process. In STS measurement, the normalized conductance (dI/dV/I/V) versus V curves indicate nearly metallic band gap, at the boundaries of Fe (or Fe{sub 3}C) nanoparticles. Microstructural analysis indicates that the mechanism for improved EFE properties is due to the formation of nanographite that surrounds the Fe (or Fe{sub 3}C) nanoparticles.

  15. Effect of substrate temperature on the growth and properties of boron-doped microcrystalline silicon films

    Institute of Scientific and Technical Information of China (English)

    Lei Qing-Song; Wu Zhi-Meng; Geng Xin-Hua; Zhao Ying; Sun Jian; Xi Jian-Ping

    2006-01-01

    Highly conductive boron-doped hydrogenated microcrystalline silicon (μc-Si:H) films are prepared by very high frequency plasma enhanced chemical vapour deposition (VHF PECVD) at the substrate temperatures (Ts) ranging from 90℃ to 270℃. The effects of Ts on the growth and properties of the films are investigated. Results indicate that the growth rate, the electrical (dark conductivity, carrier concentration and Hall mobility) and structural (crystallinity and grain size) properties are all strongly dependent on Ts. As Ts increases, it is observed that 1) the growth rate initially increases and then arrives at a maximum value of 13.3 nm/min at Ts=210℃, 2) the crystalline volume fraction (Xc) and the grain size increase initially, then reach their maximum values at Ts = 140℃, and finally decrease, 3) the dark conductivity (σd),carrier concentration and Hall mobility have a similar dependence on Tg and arrive at their maximum values at Ts=190℃. In addition, it is also observed that at a lower substrate temperature Ts, a higher dopant concentration is required in order to obtain a maximum σd.

  16. Preparation of Cellulose/Chitosan Composite Biosorbents for Removal of Heavy Metal Ions%纤维素/壳聚糖复合吸附剂的制备及其对重金属离子吸附的研究

    Institute of Scientific and Technical Information of China (English)

    胡剑灿; 肖敏; 李改利

    2016-01-01

    将纤维素和壳聚糖溶于乙二胺/硫氰酸钾溶液中,混合,以甲醇为凝固浴析出制备了环境友好的纤维素/壳聚糖复合物。红外光谱显示,在复合物中纤维素和壳聚糖间形成了分子间氢键作用。 XRD谱图显示复合物中纤维素的结晶度下降,有利用金属离子扩散到复合物内部。 Cu2+和Pb2+的二元离子溶液吸附实验显示Cu2+和Pb2+之间存在着竞争吸附。%Environment -friendly cellulose/chitosan composite was prepared by coagulating a blend of cellulose and chitosan in ethylenediamine/potassium sulfocyanate solution with methanol as coagulant .Infrared spectra indicated the intermolecular hydrogen bond between cellulose and chitosan .X-ray diffraction patterns indicated that the crystallinity of cellulose in composite was lower than in pure cellulose , and metal ions could more easily penetrate into the composite . Adsorption isotherms for Cu(II) and Pb(II) binary solutions showed that there were competition effects between the two kinds of metal ions .

  17. Fabrication of Cellulose Nanofiber/AlOOH Aerogel for Flame Retardant and Thermal Insulation

    OpenAIRE

    Bitao Fan; Shujun Chen; Qiufang Yao; Qingfeng Sun; Chunde Jin

    2017-01-01

    Cellulose nanofiber/AlOOH aerogel for flame retardant and thermal insulation was successfully prepared through a hydrothermal method. Their flame retardant and thermal insulation properties were investigated. The morphology image of the cellulose nanofiber/AlOOH exhibited spherical AlOOH with an average diameter of 0.5 μm that was wrapped by cellulose nanofiber or adhered to them. Cellulose nanofiber/AlOOH composite aerogels exhibited excellent flame retardant and thermal insulation propertie...

  18. Investigation of the physico-mechanical properties of electrospun PVDF/cellulose nanofibers.

    OpenAIRE

    Issa, A. A. [احمد عبد السلام عيسى; Al-Maadeed, M.; Luyt,A.S.; Mrlik, M.; Hassan, M. K.

    2016-01-01

    The electro-activity and mechanical properties of PVDF depends mainly on the b-phase content and degree of crystallinity. In this study, cellulose fibers were used to improve these characteristics. This could be achieved because the hydroxyl groups on cellulose would force the fluorine atoms in PVDF to be in the trans-conformation, and the cellulose particles could act as nucleation centers. Electrospinning was used to prepare the PVDF/cellulose (nano)fibrous films, and this improved the tota...

  19. Preparation and characterization of novel fast disintegrating capsules (Fastcaps) for administration in the oral cavity.

    Science.gov (United States)

    Ciper, Mesut; Bodmeier, Roland

    2005-10-13

    The objective of this study was to prepare novel capsule-based fast disintegrating dosage forms for the oral cavity (Fastcaps). First, cast films were prepared from various additive-containing gelatin solutions and evaluated with respect to disintegration time and mechanical properties in order to identify suitable formulations for the capsule preparation. The disintegration time of films decreased with decreasing bloom strength and could be further decreased by the addition of sugars or PEGs. Fast disintegrating capsules were successfully prepared by a dipping process, whereby parameters such as the viscosity and temperature of the dipping solution and the dipping velocity of the steel pins were optimized. The required viscosity range of the dipping solution for Fastcap manufacturing was 500-600 cP. The addition of the hydrophilic additives (xylitol, sorbitol or PEG 1500) did not significantly affect the viscosity and gelation temperature of the dipping solution. The in vitro disintegration of Fastcaps (30-45 s) was twice as rapid as the one of regular hard gelatin capsules. In vivo, Fastcaps disintegrated rapidly (9-13 s) and their content was spread throughout the oral cavity within seconds. Lactose and/or microcrystalline cellulose were suitable fillers for Fastcaps. The mechanical properties of Fastcaps were similar to commercially available gelatin capsules, which assures good processability and handling.

  20. Preparation

    Directory of Open Access Journals (Sweden)

    M.M. Dardir

    2014-03-01

    Full Text Available Some hexanamide-mono and di-linoleniate esters were prepared by the reaction of linolenic acid and hexanamide (derived from the reaction of hexanoic acid and diethanolamine. The chemical structure for the newly prepared hexanamide-mono and di-linoleniate esters were elucidated using elemental analysis, (FTIR, H 1NMR and chemical ionization mass spectra (CI/Ms spectroscopic techniques. The results of the spectroscopic analysis indicated that they were prepared through the right method and they have high purity. The new prepared esters have high biodegradability and lower toxicity (environmentally friendly so they were evaluated as a synthetic-based mud (ester-based mud for oil-well drilling fluids. The evaluation included study of the rheological properties, filtration and thermal properties of the ester based-muds formulated with the newly prepared esters compared to the reference commercial synthetic-based mud.