Electrochemical Functionalization in Wavefunction Engineering of Epitaxial Graphene

2014 ◽  
Vol 1658 ◽  
Author(s):  
Santanu Sarkar

ABSTRACTChemical modification of graphene web has attracted strong interest in engineering a band gap in graphene and in altering its magnetic and solubility properties. Electrochemical methods to functionalize graphene have emerged as attractive protocols to covalently modify graphene. Kolbe reaction, which involves the electrochemical oxidation of arylacetates (generation of α-naphthylmethyl radicals, in our present case), allows reversible grafting of radicals to graphene surface; the electro-erasing of the functional groups leads to graphene at its nearly pristine state. The surface coverage can be controlled from densely-packed (ideal as organic dielectrics) to sparsely functionalized surface (ideal for introducing reasonable band gap in graphene) with well-ordered structural patterning of the functional groups on EG surface by fine adjustment of electrochemical conditions. Such a control of the layer structure and packing of the functional groups over the graphene surface is an essential issue in the development of graphene chemistry.

2018 ◽  
Vol 1 (1) ◽  
pp. 114-124 ◽  
Author(s):  
Jesie Silva ◽  
Lizebel Morante ◽  
Tesfamichael Demeke ◽  
Jacqueline Baah-Twum ◽  
Abel Navarro

The prevalence of antibiotics in water creates microbial resistance and has a negative impact on the ecosystem. Biomaterials such as spent tea leaves are rich in functional groups and are suitable for chemical modification for diverse applications. This research proposes the use of spent tea leaves of chamomile (CM), green tea (GT), and peppermint (PM) as structural scaffolds for the incorporation of carboxyl, sulfonyl, and thiol groups to improve the adsorption of Penicillin G (Pe). Adsorbents characterization reported a higher number of acidic functional groups, mainly in thiolated products. Scanning electron microscopy (SEM) analysis showed changes on the surfaces of the adsorbents due to reaction conditions, with a stronger effect on thiolated and sulfonated adsorbents. Elemental analysis by Energy dispersive X-ray spectrophotometry (EDS) corroborated the chemical modification by the presence of sulfur atoms and the increase in oxygen/carbon ratios. Batch experiments at different pH shows a strong pH-dependence with a high adsorption at pH 8 for all the adsorbents. The adsorption follows the trend CMs > GTs > PMs. Thiolation and sulfonation reported higher adsorptions, which is most likely due to the sulfur bridge formation, reaching adsorption percentages of 25%. These results create a new mindset in the use of spent tea leaves and their chemical modifications for the bioremediation of antibiotics.


2012 ◽  
Vol 573-574 ◽  
pp. 31-34
Author(s):  
Li Ge Wang ◽  
Fan Zhang ◽  
Yang Zhang ◽  
Long Zhou ◽  
En Ze Wang

A new type of pellet binder was prepared with oxalic acid as sodium silicate chemical modification agent in this paper, the compressive strength of which improved obviously. It improved from 0.6 KN/a to 2.4 KN/a, when the amount of oxalic acid is 8%. Meanwhile, carboxyl introduced at 390°C started carbonization decomposition, and pelletizing properties wouldn't be affected without new pellet impurity. The analysis shows that adding oxalic acid introduces carboxyl only in the binder, but doesn't generate new functional groups; Polymer layer formed by carboxyl adsorption on sodium silicate gel particle surface limits colloidal particle growing up, and plays roles of refining colloidal particle and improving the bonding strength.


2019 ◽  
Vol 85 (3) ◽  
pp. 30101
Author(s):  
Xinyue Zhang ◽  
Qingsong Huang

Symmetry of adsorption site is the key to control the graphene band gap. When the adsorption sites change from mirror-symmetry adsorption (MSA) to mirror antisymmetric adsorption (MAA) position, the bandgap change (BC) exhibits two opposite tendencies. Therefore, a standard was developed to determine the type of band gap modification of graphene. When BC is negative, the bonding state between the adsorbent and graphene was the dominant factor. When BC is positive, the built-in electric field becomes dominated. Continuous tuning of the band gap can be achieved by adsorbing the appropriate functional groups. Our findings set the standard for determining the type of band gap modification and open the way for controllable adjustment of graphene band gap.


2020 ◽  
Vol 12 (2) ◽  
pp. 734 ◽  
Author(s):  
Menisha S. Karunarathna ◽  
Rhett C. Smith

Lignin is the most abundant aromatic biopolymer and is the sustainable feedstock most likely to supplant petroleum-derived aromatics and downstream products. Rich in functional groups, lignin is largely peerless in its potential for chemical modification towards attaining target properties. Lignin’s crosslinked network structure can be exploited in composites to endow them with remarkable strength, as exemplified in timber and other structural elements of plants. Yet lignin may also be depolymerized, modified, or blended with other polymers. This review focuses on substituting petrochemicals with lignin derivatives, with a particular focus on applications more significant in terms of potential commercialization volume, including polyurethane, phenol-formaldehyde resins, lignin-based carbon fibers, and emergent melt-processable waste-derived materials. This review will illuminate advances from the last eight years in the prospective utilization of such lignin-derived products in a range of application such as adhesives, plastics, automotive components, construction materials, and composites. Particular technical issues associated with lignin processing and emerging alternatives for future developments are discussed.


1981 ◽  
Vol 54 (3) ◽  
pp. 596-626 ◽  
Author(s):  
Alan R. Luxton

Abstract This review will be restricted to the applications of liquid polybutadienes (BR) which, as prepared, are devoid of functional groups other than the unsaturation left after polymerization. These products should not be confused with the so called telechelic BRs in which terminal functional groups are deliberately introduced during preparation. The preparative techniques and applications relating to the latter polymers have been described both by French and more recently by Athey. For many applications, it is necessary to introduce functional groups into the “nonfunctional” liquid BRs as a subsequent stage to polymerization. However, such chemical modification is often carried out to yield a relatively high level of functionality and, more significantly, the functional groups are randomly distributed along the polymer backbone. Therefore, there is still a clear distinction between chemically modified, nonfunctional BRs and the telechelic polymers. Whereas the latter have often been included under the “liquid rubber” classification, this term would be incorrect for the nonfunctional BRs with respect to the majority of their applications. Liquid BRs are not a new range of materials. To the writer's knowledge the first commercial liquid BR to be produced by a polymerization process was Plastikator 32. This polymer was produced in Germany, apparently from about 1925. Between about 1950 and the mid-1960s many of the major polymer producing companies developed production techniques and investigated the applications of liquid BRs. However, with the notable exceptions of Du pont's “Budium” and the Richardson Co.'s “Ricon” range (formerly known as Enjay Buton and now manufactured by Colorado Chemicals Specialities Inc.), they did not become fully commercial. It was not until the late 1960s and early 1970s that liquid BRs achieved significant commercial tonnages. This was largely associated with the advent, in Western Europe and Japan, of the use of liquid BRs as the feedstock for electrodeposition primers for car bodies and for chlorinated rubber paints and inks. A reasonable estimate for annual production of liquid BRs in the mid-1970s would be between 8000 and 15 000 (tons.) This ready commercial availability of liquid BRs, encompassing a wide range of microstructure and molecular weight (M.W.) has prompted an equally wide ranging evaluation of their potential applications. It is impossible to define a M.W. above which a BR is no longer construed as being a liquid. BRs up to a M.W. around 50×103 have been included in this loose definition, but the most common range is 1×103−10×103. Apart from M.W. and molecular weight distribution, M.W.D., the viscosity of a BR is very dependent upon the polymer structure. The same parameters which affect viscosity also have a strong influence on the chemical modification and application properties of liquid BRs. Previous articles describing applications of liquid BRs have tended to concentrate on products having a particular type of microstructure. Since the technique of preparation often controls the microstructure and M.W.D., it is relevant to describe aspects of the preparation and chemical modification as a prelude to discussing the applications of liquid BRs.


2020 ◽  
Vol 21 (2) ◽  
pp. 487 ◽  
Author(s):  
Wenqian Wang ◽  
Qiuyu Meng ◽  
Qi Li ◽  
Jinbao Liu ◽  
Mo Zhou ◽  
...  

Chitosan is a product of the deacetylation of chitin, which is widely found in nature. Chitosan is insoluble in water and most organic solvents, which seriously limits both its application scope and applicable fields. However, chitosan contains active functional groups that are liable to chemical reactions; thus, chitosan derivatives can be obtained through the chemical modification of chitosan. The modification of chitosan has been an important aspect of chitosan research, showing a better solubility, pH-sensitive targeting, an increased number of delivery systems, etc. This review summarizes the modification of chitosan by acylation, carboxylation, alkylation, and quaternization in order to improve the water solubility, pH sensitivity, and the targeting of chitosan derivatives. The applications of chitosan derivatives in the antibacterial, sustained slowly release, targeting, and delivery system fields are also described. Chitosan derivatives will have a large impact and show potential in biomedicine for the development of drugs in future.


Author(s):  
Eiichi Kuramochi ◽  
Masaya Notomi ◽  
Toshiaki Tamamura ◽  
Takayuki Kawashima ◽  
Shojiro Kawakami ◽  
...  

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