scispace - formally typeset
Search or ask a question

Showing papers on "N-Methylmorpholine N-oxide published in 2017"


Journal ArticleDOI
Lili Zhang1, Hailong Lu1, Juan Yu1, Zhiguo Wang1, Yimin Fan1, Xiaofan Zhou1 
TL;DR: After the dissolution-regeneration process of LCs, the fiber bundles of the LCs disappeared and the crystal type of cellulose in theLCs was transformed from cellulose I to cellulose II, which indicated the complete dissolution ofLCs.
Abstract: Lignocelluloses (LCs) with various amounts of lignin (even as high as 18.4%) were successfully dissolved in N-methylmorpholine-N-oxide monohydrate (NMMO/H2O) solution with stirring at 85 °C within 5 h. For the developmental dissolution methods of LCs with a high lignin content in NMMO/H2O solution, the following two pretreatment steps of LCs were necessary: (1) glycerol swelling and (2) mechanical extrusion. The mechanical extrusion pretreatment under glycerol swelling dissociated the fiber bundles of LCs to thinner fibers and, thus, enhanced the accessibility and solubility of the LCs in NMMO/H2O. The crystal structure of the pretreated LCs had no significant transformation during pretreatment, while the diameters of the fiber bundles were reduced from 50–60 to 10–12 μm, as investigated by X-ray diffraction and scanning electron microscopy. After the dissolution–regeneration process of LCs, the fiber bundles of the LCs disappeared and the crystal type of cellulose in the LCs was transformed from cellulos...

36 citations


Journal ArticleDOI
TL;DR: In this article, a method for synthesis of silver nanoparticles in N-methylmorpholine Noxide (NMMO) and the associated mechanism, as well as their use for in-situ volume modification of cellulose fibers, was presented.
Abstract: We present a method for synthesis of silver nanoparticles in N-methylmorpholine N-oxide (NMMO) and the associated mechanism, as well as their use for in situ volume modification of cellulose fibers. The synthesized particles had diameter of about 4 nm, and their colloid solution was stable for 1 year. The nanoparticles were stabilized using polyethylenimine, which apart from preventing nanoparticle agglomeration, also accelerated Ag+ ion reduction and prevented NMMO degradation. A mechanism for the nanoparticle synthesis is suggested based on the electrochemical potentials of all ions in solution, with perhydroxyl ions resulting from NMMO reducing the silver ions. We also created nanocomposites from fibers and silver nanoparticles, in which the latter showed very good dispersion in the fiber volume. Such spun fibers showed improved mechanical parameters in comparison with unmodified fibers.

17 citations


Journal ArticleDOI
TL;DR: In this paper, solid-state dissolution of cellulose in N-methylmorpholine-Noxide with added tetraethoxysilane (TEOS) was shown to increase up to 16% the fiber carbon residue during heat treatment.
Abstract: Composite fibers were prepared by solid-state dissolution of cellulose in N-methylmorpholine-N-oxide with added tetraethoxysilane (TEOS). It was shown that adding TEOS to the cellulose matrix increased up to 16% the fiber carbon residue during heat treatment. Bonds formed between Si and C during their high-temperature treatment according to IR spectra of the composite cellulose fibers. The thermal behavior of the fibers was studied using TGA and TMA. The fiber morphology and the structure of the Si-containing additive particles were examined using SEM and TEM. The mechanical properties of carbon fibers prepared from cellulose-hydrate and composite fibers were compared.

11 citations


Journal ArticleDOI
TL;DR: In this article, N-methylmorpholine-Noxide (NMMO)/H2O was used as a homogeneous reaction medium for the cellulose alkalization process to intensify the alkalisation degree and improve the substitution uniformity.
Abstract: Alkali cellulose is an important intermediate in the production of cellulose derivatives. N-methylmorpholine-N-oxide (NMMO)/H2O was used as a homogeneous reaction medium for the cellulose alkalization process to intensify the alkalization degree and improve the substitution uniformity. The morphology, specific surface area and crystalline structure of pristine cellulose, the as-synthesized alkali cellulose and dissolved-regenerated cellulose were characterized by SEM, BET, XRD and FT-IR, respectively. The results showed that the homogeneous reaction medium not only offered a low mass transfer resistance, but also facilitated a disruption of the hydrogen bond in cellulose, thus resulting in the transformation of the cellulose structure from complicated stacking chains to simple glucose chains. The interior hydroxyl groups in the cellulose became accessible to the alkaline reagent NaOH to enhance the alkalization process for the increase in bonding alkali content and the improvement in substitution uniformity. The bonding alkali content was calculated by the difference between total added alkali and free alkali and was achieved as 0.61 g/g cellulose at the optimized operation conditions: reaction temperature of 95 °C, reaction time of 90 min, NMMO dosage of 90.00 g, cellulose 1.0 g and NaOH concentration of 1.40 wt%. Meanwhile, in the conventional alkalization process, the bonding alkali content was just 0.41 g/g cellulose. The alkali cellulose prepared in NMMO/H2O medium has a large specific surface area of 125 m2 g−1 and an extremely low crystallinity degree. The NMMO/H2O system represents a potential homogeneous solvent for the cellulose alkalization process.

9 citations


Journal ArticleDOI
TL;DR: In this paper, it was shown that N-Methylmorpholine-Noxide (NMMO) cannot be completely separated from mixtures with common 1,3-dialkylimidazolium ionic liquids (ILs) due to strong ionic interactions between the two components.
Abstract: N-Methylmorpholine-N-oxide (NMMO) cannot be completely separated by extraction from mixtures with common 1,3-dialkylimidazolium ionic liquids (ILs) due to strong ionic interactions between the two components. At elevated temperatures, above approx. 90 °C, especially under dry conditions and in the presence of acid, alkylating or acylating agents, remaining NMMO in ILs tends to undergo autocatalytic degradation. This is a highly exothermic, unstoppable process that results in explosions, flames, and complete charring of the reaction mixtures. Thus, caution must be exercised when drying or heating ILs that were in previous contact with NMMO, and the absence of amine oxide must be confirmed to avoid potential danger.

7 citations


Journal ArticleDOI
TL;DR: Water-dispersible single-walled carbon nanotubes (SWCNTs) were prepared through successive treatments with chlorosulfuric acid (CSA)/H2O2 and N-methylmorpholine N-oxide (NMO) monohydrate and elucidated based on the high polarity of the NMO molecule to highlight the wide applicability of these nanocarbon materials.
Abstract: Dispersion of nanocarbon materials in liquid media, via solution processing such as spraying, printing, spinning, etc. is one of the prerequisites for practical applications. Here we report that water-dispersible single-walled carbon nanotubes (SWCNTs) were prepared through successive treatments with chlorosulfuric acid (CSA)/H2O2 and N-methylmorpholine N-oxide (NMO) monohydrate. The powder of the CSA/H2O2- and NMO-treated SWCNTs (N-SWCNTs) could be readily redispersed in water in concentrations as high as 1 g l-1 without requiring a dispersant. The mechanism responsible for the high dispersity of the N-SWCNT powder in polar solvents, including water, was elucidated based on the high polarity of the NMO molecule. In order to highlight the wide applicability of the N-SWCNTs, they were used successfully to prepare conducting thin films by spray-coating plastic substrates with an aqueous hybrid solution containing the N-SWCNTs and Ag nanowires (NWs). In addition, a flexible, large-area thin-film heater was prepared based on the N-SWCNT/AgNW hybrid film with a transmittance of 93% and sheet resistance of 30 Ω sq-1.

5 citations