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.

Effect of Acid on Surface Hydroxyl Groups on Kaolinite and Montmorillonite

2018 ◽  
Vol 232 (3) ◽  
pp. 409-430 ◽  
Author(s):  
Sarah K. Sihvonen ◽  
Kelly A. Murphy ◽  
Nancy M. Washton ◽  
Muhammad Bilal Altaf ◽  
Karl T. Mueller ◽  
...  
Keyword(s):  
Functional Groups ◽  
Acid Treatment ◽  
Atmospheric Transport ◽  
Magic Angle Spinning ◽  
Resonance Spectroscopy ◽  
Hydroxyl Groups ◽  
Magic Angle ◽  
Surface Hydroxyl ◽  
Surface Hydroxyl Groups ◽  
Angle Spinning

AbstractMineral dust aerosol participates in heterogeneous chemistry in the atmosphere. In particular, the hydroxyl groups on the surface of aluminosilicate clay minerals are important for heterogeneous atmospheric processes. These functional groups may be altered by acidic processing during atmospheric transport. In this study, we exposed kaolinite (KGa-1b) and montmorillonite (STx-1b) to aqueous sulfuric acid and then rinsed the soluble reactants and products off in order to explore changes to functional groups on the mineral surface. To quantify the changes due to acid treatment of edge hydroxyl groups, we use19F magic angle spinning nuclear magnetic resonance spectroscopy and a probe molecule, 3,3,3-trifluoropropyldimethylchlorosilane. We find that the edge hydroxyl groups (OH) increase in both number and density with acid treatment. Chemical reactions in the atmosphere may be impacted by the increase in OH at the mineral edge.

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.

Soil Chemistry

2003 ◽  
Author(s):  
Anthony S. R. Juo ◽  
Kathrin Franzluebbers
Keyword(s):  
Surface Charge ◽  
Functional Groups ◽  
Soil Chemistry ◽  
Chemical Properties ◽  
Hydroxyl Groups ◽  
Oh Groups ◽  
Surface Hydroxyl ◽  
Mineral Structure ◽  
Ph Dependent ◽  
Soil Colloids

Soil chemistry deals with the chemical properties and reactions of soils. It is essentially the application of electrochemistry and colloid chemistry to soil systems. Major topics include surface charge properties of soil colloids, cation and anion sorption and exchange, soil acidity, soil alkalinity, soil salinity, and the effects of these chemical properties and processes on soil biological activity, plant growth, and environmental quality. The ability of the electrically charged surface of soil colloids to retain nutrient cations and anions is an important chemical property affecting the fertility status of the soil. There are two major sources of electrical charges on soil organic and inorganic colloids, namely, permanent or constant charges and variable or pH-dependent charges. Permanent or constant charges are the result of the charge imbalance brought about by isomorphous substitution in a mineral structure of one cation by another of similar size but differing valence (see also section 2.3.2). For example, the substitution of Mg2+ for Al3+ that occurs in Al-dominated octahedral sheets of 2:1 clay minerals results in a negative surface charge in smectite, vermiculite, and chlorite. The excess negative charges are then balanced by adsorbed cations to maintain electrical neutrality. Permanent negative charges of all 2:1 silicate minerals arise from isomorphous substitutions. The l:l-type clay mineral, kaolinite, has only a minor amount of permanent charge due to isomorphic substitution. The negative charges on kaolinite originate from surface hydroxyl groups on the edge of the mineral structure and are pH-dependent. Variable or pH-dependent charges occur on the surfaces of Fe and Al oxides, allophanes, and organic soil colloids. This type of surface charge originates from hydroxyl groups and other functional groups by releasing or accepting H+ ions, resulting in either negative or positive charges. Other functional groups are hydroxyl (OH) groups of Fe and/or Al oxides and allophanes and the COOH and OH groups of soil organic matter. Variable-charge soil colloids bear either a positive or a negative net surface charge depending on the pH of the soil. The magnitude of the charge varies with the electrolyte concentration of the soil solution.

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.

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 Mechanical Properties of Graphene Oxide Coupled by Multi-Physical Field: Grain Boundaries and Functional Groups

Crystals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 62
Author(s):  
Xu Xu ◽  
Zeping Zhang ◽  
Wenjuan Yao
Keyword(s):  
Mechanical Properties ◽  
Graphene Oxide ◽  
Grain Boundaries ◽  
Functional Groups ◽  
Oxygen Content ◽  
Tensile Fracture ◽  
Hydroxyl Groups ◽  
Molecular Configuration ◽  
Spatial Design ◽  
Out Of Plane

Graphene and graphene oxide (GO) usually have grain boundaries (GBs) in the process of synthesis and preparation. Here, we “attach” GBs into GO, a new molecular configuration i.e., polycrystalline graphene oxide (PGO) is proposed. This paper aims to provide an insight into the stability and mechanical properties of PGO by using the molecular dynamics method. For this purpose, the “bottom-up” multi-structure-spatial design performance of PGO and the physical mechanism associated with the spatial structure in mixed dimensions (combination of sp2 and sp3) were studied. Also, the effect of defect coupling (GBs and functional groups) on the mechanical properties was revealed. Our results demonstrate that the existence of the GBs reduces the mechanical properties of PGO and show an “induction” role during the tensile fracture process. The presence of functional groups converts in-plane sp2 carbon atoms into out-of-plane sp3 hybrid carbons, causing uneven stress distribution. Moreover, the mechanical characteristics of PGO are very sensitive to the oxygen content of functional groups, which decrease with the increase of oxygen content. The weakening degree of epoxy groups is slightly greater than that of hydroxyl groups. Finally, we find that the mechanical properties of PGO will fall to the lowest values due to the defect coupling amplification mechanism when the functional groups are distributed at GBs.

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.

A poly(arylene ether sulfone) hybrid membrane using titanium dioxide nanoparticles as the filler

2016 ◽  
Vol 29 (1) ◽  
pp. 26-35 ◽  
Author(s):  
Yunwu Yu ◽  
Wenhao Pan ◽  
Xiaoman Guo ◽  
Lili Gao ◽  
Yaxin Gu ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Titanium Dioxide ◽  
Gas Separation ◽  
Proton Nuclear Magnetic Resonance ◽  
Separation Performance ◽  
Hydroxyl Groups ◽  
Hybrid Membranes ◽  
Permeability Coefficients ◽  
Arylene Ether ◽  
The Matrix

Poly(arylene ether sulfone) (PES)–titanium dioxide (TiO2) hybrid membranes were prepared via solution blending method using TiO2 nanoparticles as inorganic filler. The chemical structure and thermal stability of the matrix polymer were characterized by proton nuclear magnetic resonance, Fourier transform infrared, differential scanning calorimetry, and thermogravimetric analysis. The crystal structure, morphology, mechanical properties, and gas separation performance of hybrid membranes were characterized in detail. As shown in scanning electron microscopic images, TiO2 nanoparticles dispersed homogeneously in the matrix. Although the mechanical properties of hybrid membranes decreased certainly compared to the pure PES membranes, they are strong enough for gas separation in this study. All gas permeability coefficients of PES-TiO2 hybrid membranes were higher than pure PES membranes, attributed to the nanogap caused by TiO2 nanoparticles, for instance, oxygen and nitrogen permeability coefficients of Hybrid-3 (consists of PES with 4-amino-phenyl pendant group and hexafluoroisopropyl (Am-PES)-20 and TiO2 nanoparticles, 5 wt%) increased from 2.57 and 0.33 to 5.88 and 0.63, respectively. In addition, the separation factor increased at the same time attributed to the stimulative transfer effect caused by the interaction of hydroxyl groups on the TiO2 nanoparticle and polar carbon dioxide molecules.

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