Biodegradation of chemically modified lignocellulosic sisal fibers: study of the mechanism for enzymatic degradation of cellulose

e-Polymers ◽  
2015 ◽  
Vol 15 (3) ◽  
pp. 185-194 ◽  
Author(s):  
Prosenjit Saha ◽  
Debasis Roy ◽  
Suvendu Manna ◽  
Sukanya Chowdhury ◽  
Sruti Banik ◽  
...  
Keyword(s):  
Amorphous Materials ◽  
Fiber Surface ◽  
Crystalline Cellulose ◽  
Hydroxyl Groups ◽  
Biological Degradation ◽  
Soil Burial ◽  
Surface Hydroxyl ◽  
Lignocellulosic Fibers ◽  
Sisal Fibers ◽  
Hydrolysis Of

AbstractThe susceptibility and characteristics of biological degradation of lignocellulosic fibers, such as sisal fibers, are presented in this study using a modified soil burial test (SBT) protocol. The biodegradation profile of untreated sisal fibers as well as of fibers treated with an alkaline emulsion of neem oil and phenolic resin was evaluated by estimating the enzymatic activities during the exposure of fibers to a soil/compost mix. Observation of the results indicated that biodegradation of the fibers was predominated by enzymatic hydrolysis of amorphous materials followed by degradation of crystalline cellulose. It was also evident that “oil-resin” treatment makes the fibers more resistant to biodegradation owing to the removal of amorphous materials, enhanced hydrophobicity, and possible chemical alteration of the surface hydroxyl groups of the fiber surface. This research aims to establish a systematic knowledge on the biodegradation profile of fiber components using a state-of-the-art protocol for SBT.

Synthesis and Characterization of TiO2/ PSt/PVP Multilayer Core-Shell Hybrid Microspheres

2012 ◽  
Vol 512-515 ◽  
pp. 2443-2447 ◽  
Author(s):  
Li Ying Guo
Keyword(s):  
Decomposition Temperature ◽  
Tetrabutyl Titanate ◽  
Core Shell ◽  
Hydroxyl Groups ◽  
Surface Hydroxyl ◽  
Surface Hydroxyl Groups ◽  
Ft Ir ◽  
Hydrolysis Of ◽  
Thermal Stability Of

Multiplayer core-shell TiO2/PSt/PVP hybrid microspheres were successfully synthesized by the copolymerization of vinylpyrrolidone in the solution of ethyl acetate with TiO2/PSt core-shell hybrid microspheres which were formed through the encapsulation of KH570-g-TiO2 sol particles with styrene, while the active KH570-g-TiO2 sol particles were prepared by the hydrolysis condensation of KH-570 with tetrabutyl titanate. Characterization technologies of FT-IR and TGA were applied to investigate the structure and the thermal stability of the product. The results showed that the hydroxyl groups from the hydrolysis of KH-570 condensed with the surface hydroxyl groups of TiO2, as well as PSt and PVP were grafted successively onto the surface of KH570-g-TiO2 sol particles. The thermal decomposition temperature of TiO2/PSt/PVP was higher than TiO2/PSt, which also indicated that the obtained product was the final objective product.

scholarly journals Features of Functionalization of the Surface of Alumina Nanofibers by Hydrolysis of Organosilanes on Surface Hydroxyl Groups

Polymers ◽  
2021 ◽  
Vol 13 (24) ◽  
pp. 4374
Author(s):  
Mikhail M. Simunin ◽  
Anton S. Voronin ◽  
Yurii V. Fadeev ◽  
Yurii L. Mikhlin ◽  
Denis A. Lizunov ◽  
...  
Keyword(s):  
Functional Groups ◽  
Simultaneous Thermal Analysis ◽  
Hydroxyl Groups ◽  
Surface Hydroxyl ◽  
Alumina Nanofibers ◽  
High Uniformity ◽  
The Matrix ◽  
Important Approach ◽  
Hydrolysis Of ◽  
Perfect Interface

Small additions of nanofiber materials make it possible to change the properties of polymers. However, the uniformity of the additive distribution and the strength of its bond with the polymer matrix are determined by the surface of the nanofibers. Silanes, in particular, allow you to customize the surface for better interaction with the matrix. The aim of our work is to study an approach to silanization of nanofibers of aluminum oxide to obtain a perfect interface between the additive and the matrix. The presence of target silanes on the surface of nanofibers was shown by XPS methods. The presence of functional groups on the surface of nanofibers was also shown by the methods of simultaneous thermal analysis, and the stoichiometry of functional groups with respect to the initial hydroxyl groups was studied. The number of functional groups precipitated from silanes is close to the number of the initial hydroxyl groups, which indicates a high uniformity of the coating in the proposed method of silanization. The presented technology for silanizing alumina nanofibers is an important approach to the subsequent use of this additive in various polymer matrices.

The synthesis and structure of silica-supported bis(h5-cyclopentadienyl)dichlorotitanium(IV) complexes

1986 ◽  
Vol 51 (7) ◽  
pp. 1430-1438 ◽  
Author(s):  
Alena Reissová ◽  
Zdeněk Bastl ◽  
Martin Čapka
Keyword(s):  
Free Surface ◽  
Hydroxyl Groups ◽  
Titanium Complex ◽  
Surface Hydroxyl ◽  
Surface Hydroxyl Groups ◽  
Free Hydroxyl ◽  
Cyclopentadienyl Anion

The title complexes have been obtained by functionalization of silica with cyclopentadienylsilanes of the type Rx(CH3)3 - xSi(CH2)nC5H5 (x = 1-3, n = 0, 1, 3), trimethylsilylation of free surface hydroxyl groups, transformation of the bonded cyclopentadienyl group to the cyclopentadienyl anion, followed by coordination of (h5-cyclopentadienyl)trichlorotitanium. The effects of single steps of the above immobilization on texture of the support, the number of free hydroxyl groups, the coverage of the surface by cyclopentadienyl groups and the degree of their utilization in anchoring the titanium complex have been investigated. ESCA study has shown that the above anchoring leads to formation of the silica-supported bis(h5-cyclopentadienyl)dichlorotitanium(IV) complex.

scholarly journals Adjustment of Hydrophobic Properties of Cellulose Materials

Polymers ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 1241
Author(s):  
Michael Ioelovich
Keyword(s):  
Ester Group ◽  
Hydroxyl Groups ◽  
Chemical Methods ◽  
Hydrophobic Properties ◽  
Cellulose Esters ◽  
Cellulose Modification ◽  
Polar Groups ◽  
Polar Substituents ◽  
Hydrolysis Of ◽  
Cellulose Materials

In this study, physicochemical and chemical methods of cellulose modification were used to increase the hydrophobicity of this natural semicrystalline biopolymer. It has been shown that acid hydrolysis of the initial cellulose increases its crystallinity, which improves hydrophobicity, but only to a small extent. A more significant hydrophobization effect was observed after chemical modification by esterification, when polar hydroxyl groups of cellulose were replaced by non-polar substituents. The esterification process was accompanied by the disruption of the crystalline structure of cellulose and its transformation into the mesomorphous structure of cellulose esters. It was found that the replacement of cellulose hydroxyls with ester groups leads to a significant increase in the hydrophobicity of the resulting polymer. Moreover, the increase of the number of non-polar groups in the ester substituent contributes to rise in hydrophobicity of cellulose derivative. Depending on the type of ester group, the hydrophobicity increased in the following order: acetate < propionate < butyrate. Therefore, tributyrate cellulose (TBC) demonstrated the most hydrophobicity among all studied samples. In addition, the mixed ester, triacetobutyrate cellulose (TAB), also showed a sufficiently high hydrophobicity. The promising performance properties of hydrophobic cellulose esters, TBC and TAB, were also demonstrated.

scholarly journals High catalytic activity for formaldehyde oxidation of an interconnected network structure composed of δ-MnO2 nanosheets and γ-MnOOH nanowires

2020 ◽  
Vol 8 (4) ◽  
pp. 429-439
Author(s):  
Ying Tao ◽  
Rong Li ◽  
Ai-Bin Huang ◽  
Yi-Ning Ma ◽  
Shi-Dong Ji ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Network Structure ◽  
Manganese Oxides ◽  
Active Oxygen Species ◽  
Low Cost ◽  
High Dispersion ◽  
Hydroxyl Groups ◽  
High Catalytic Activity ◽  
Interconnected Network ◽  
Surface Hydroxyl

AbstractAmong the transition metal oxide catalysts, manganese oxides have great potential for formaldehyde (HCHO) oxidation at ambient temperature because of their high activity, nontoxicity, low cost, and polybasic morphologies. In this work, a MnO2-based catalyst (M-MnO2) with an interconnected network structure was successfully synthesized by a one-step hydrothermal method. The M-MnO2 catalyst was composed of the main catalytic agent, δ-MnO2 nanosheets, dispersed in a nonactive framework material of γ-MnOOH nanowires. The catalytic activity of M-MnO2 for HCHO oxidation at room temperature was much higher than that of the pure δ-MnO2 nanosheets. This is attributed to the special interconnected network structure. The special interconnected network structure has high dispersion and specific surface area, which can provide more surface active oxygen species and higher surface hydroxyl groups to realize rapid decomposition of HCHO.

Improving the efficiency of enzymatic hydrolysis of Eucalyptus residues with a modified aqueous ammonia soaking method

2018 ◽  
Vol 33 (2) ◽  
pp. 165-174 ◽  
Author(s):  
Dan Huo ◽  
Qiulin Yang ◽  
Guigan Fang ◽  
Qiujuan Liu ◽  
Chuanling Si ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Enzymatic Hydrolysis ◽  
Aqueous Ammonia ◽  
Pulp Mill ◽  
Fiber Surface ◽  
Raw Material ◽  
Sem Images ◽  
Aqueous Ammonia Soaking ◽  
Guaiacyl Lignin ◽  
Hydrolysis Of

Abstract Eucalyptus residues from pulp mill were pretreated with aqueous ammonia soaking (AAS) method to improve the efficiency of enzymatic hydrolysis. The optimized condition of AAS was obtained by response surface methodology. Meanwhile, hydrogen peroxide was introduced into the AAS system to modify the AAS pretreatment (AASP). The results showed that a fermentable sugar yield of 64.96 % was obtained when the eucalypt fibers were pretreated at the optimal conditions, with 80 % of ammonia (w/w) for 11 h and keeping the temperature at 90 °C. In further research it was found that the addition of H2O2 to the AAS could improve the pretreatment efficiency. The delignification rate and enzymatic digestibility were increased to 64.49 % and 73.85 %, respectively, with 5 % of hydrogen peroxide being used. FTIR analysis indicated that most syringyl and guaiacyl lignin and a trace amount of xylan were degraded and dissolved during the AAS and AASP pretreatments. The CrI of the raw material was increased after AAS and AASP pretreatments, which was attributed to the removal of amorphous portion. SEM images showed that microfibers were separated and explored from the initial fiber structure after AAS pretreatment, and the AASP method could improve the destructiveness of the fiber surface.

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