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Abstract Carbon nanotubes [CNTs] were synthesized by the catalytic vapor decomposition method. Thereafter, they were functionalized in order to incorporate the oxygen groups (OCNT) and subsequently the amine groups (ACNT). All three CNTs (the as-synthesized and functionalized) underwent reaction with an iron organometallic complex (FePcS), iron(III) phthalocyanine-4,4",4",4""-tetrasulfonic acid, in order to study the nature of the interaction between this complex and the CNTs and the potential formation of nanocomposite materials. Transmission electronic microscopy, N2 adsorption at 77 K, thermogravimetric analysis, temperature-programmed desorption, and X-ray photoelectron spectroscopy were the characterization techniques employed to confirm the successful functionalization of CNTs as well as the type of interaction existing with the FePcS. All results obtained led to the same conclusion: There were no specific chemical interactions between CNTs and the fixed FePcS.

This work presents CO 2 activation approach towards controlled preparation of superactivated carbons (SAC) from a new lignocellulosic residue: loquat stones. This study demonstrates the potential use of loquat stones as a precursor in the preparation of SAC, reaching maximum BET surface area 3500 m 2 /g and total micropore volume 1.84 cm 3 /g. Studies on CO 2 activation at different temperatures reveal two interesting results: 1) Loquat stones can be activated at high temperatures, up to 1100 °C, achieving similar volumes of porosity with short maintenance times (30 min). 2) The greater facility for eliminating mineral matter content of the loquat stones, as well as the scarce presence of K in its composition. The high volumes both of total and narrow microporosity that are obtained in the activation of carbonized loquat stones can be explained both by the traces of mineral matter that they contain and the carbonaceous microstructure of its carbonized state. [ABSTRACT FROM AUTHOR]

A new method for radionuclide labeling by the use of graphene thin films was previously presented. In this work, a comparison among low energy radioactive sources supported on carbonaceous thin films on polyvinyl chloride-polyvinyl acetate copolymer (VYNS), based on the use of aqueous solutions is investigated as a feasible alternative to the traditional metallized films avoiding the downside of the loss of many broken films. Graphene-based materials were prepared by both oxidation-exfoliation-reduction and direct graphite exfoliation routes. In addition, multiwalled carbon nanotubes (MWCNTs) thin films were also evaluated. The stability of both carbonaceous materials aqueous dispersions were studied by using ionic and non-ionic surfactants. Solid carbon-based materials were characterized by X-Ray Diffraction (XRD) and Fourier Transform Infrared Spectroscopy (FTIR) whereas the colloidal nature of the aqueous dispersions was verified by the measurement of Tyndall effect and the morphology of thin films was evaluated by Scanning Electron Microscopy (SEM). 55 Fe solutions were used to prepare the radioactive sources on the thin films by quantitative drop deposition. The quality of spectra was measured in a pressurized proportional counter. Results showed a resolution higher than 0.9 keV for all the tested sources. However, MWCNT-based along with non-surfactant sources presented non-adequate escape peaks and low energy tails. On the contrary, all the graphene-based sources prepared using surfactants to stabilize aqueous solutions presented an energy resolution comparable to that of the metallized source while offering notable advantages in terms of cost efficiency and reliability of the as-prepared supports., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. None., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Bio-carbon-manganese composites obtained from olive mill wastewater were successfully prepared using manganese acetate as the manganese source and olive wastewater as the carbon precursor. The samples were characterized chemically and texturally by N 2 and CO 2 adsorption at 77 K and 273 K, respectively, by X-ray photoelectron spectroscopy (XPS) and X-ray diffraction. Electrochemical characterization was carried out by cyclic voltammetry (CV) and linear sweep voltammetry (LSV). The samples were evaluated in the electro-Fenton degradation of tetracycline in a typical three-electrode system under natural conditions of pH and temperature (6.5 and 25 °C). The results show that the catalysts have a high catalytic power capable of degrading tetracycline (about 70%) by a three-electron oxygen reduction pathway in which hydroxyl radicals are generated in situ, thus eliminating the need for two catalysts (ORR and Fenton).

Presently, graphenic nanomaterials are being studied as candidates for wastewater pollutant removal. In this study, two graphite oxides produced from natural graphite with different grain sizes (325 and 10 mesh), their respective reduced graphene oxides and one reduced graphene oxide with nitrogen functional groups were synthesized and tested to remove a surfactant model substrate, Triton X-100, from an aqueous solution. Kinetic experiments were carried out and adjusted to pseudo-first order equation, pseudo-second order equation, Elovich, Chain-Clayton and intra-particle diffusion models. Reduced graphene oxides displayed an instantaneous adsorption due to their accessible and hydrophobic surfaces, while graphite oxides hindered the TX100 adsorption rate due to their highly superficial oxygen content. Results from the adsorption isotherms showed that the Sips model perfectly described the TX100 adsorption behavior of these materials. Higher adsorption capacities were developed with reduced graphene oxides, being maximum for the material produced from the lower graphite grain size (q e  = 3.55·10 -6  mol/m 2 ), which could be explained by a higher surface area (600 m 2 /g), a lower amount of superficial oxygen (O/C = 0.04) and a more defected structure (I D /I G  = 0.85). Additionally, three commercial high surface area graphites in the range of 100-500 m 2 /g were evaluated for comparison purposes. In this case, better adsorption results were obtained with a more graphitic material, HSAG100 (q e  = 1.72·10 -6  mol/m 2 ). However, the best experimental results of this study were obtained using synthesized graphenic materials., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Carbon nanotubes (CNT) were prepared by a modified chemical vapor deposition (CVD) method. The synthesized carbon materials were treated with acidic and basic solutions in order to introduce certain surface functional groups, mainly containing oxygen (OCNT) or amine (ACNT) species. These modified CNTs (OCNT and ACNT) as well as the originally prepared CNT were reacted with a non-ionic Fe complex, Iron (II) Phthalocyanine, and three composites were obtained. The amount of metal complex introduced in each case and the interaction between the complex and the CNT materials were studied with the aid of various characterization techniques such as TGA, XRD, and XPS. The results obtained in these experiments all indicated that the interaction between the complex and the CNT was greatly affected by the functionalization of the latter.

A series of carbon aerogels doped with iron, cobalt and nickel have been prepared. Metal nanoparticles very well dispersed into the carbon matrix catalyze the formation of graphitic clusters around them. Samples with different Ni content are obtained to test the influence of the metal loading. All aerogels have been characterized to analyze their textural properties, surface chemistry and crystal structures. These metal-doped aerogels have a very well-developed porosity, making their mesoporosity remarkable. Ni-doped aerogels are the ones with the largest surface area and the smallest graphitization. They also present larger mesopore volumes than Co- and Fe-doped aerogels. These materials are tested as electro-catalysts for the oxygen reduction reaction. Results show a clear and strong influence of the carbonaceous structure on the whole electro-catalytic behavior of the aerogels. Regarding the type of metal doping, aerogel doped with Co is the most active one, followed by Ni- and Fe-doped aerogels, respectively. As the Ni content is larger, the kinetic current densities increase. Comparatively, among the different doping metals, the results obtained with Ni are especially remarkable.

Carbon nanotubes [CNTs] were synthesized by the catalytic vapor decomposition method. Thereafter, they were functionalized in order to incorporate the oxygen groups (OCNT) and subsequently the amine groups (ACNT). All three CNTs (the as-synthesized and functionalized) underwent reaction with an iron organometallic complex (FePcS), iron(III) phthalocyanine-4,4",4",4""-tetrasulfonic acid, in order to study the nature of the interaction between this complex and the CNTs and the potential formation of nanocomposite materials. Transmission electronic microscopy, N2 adsorption at 77 K, thermogravimetric analysis, temperature-programmed desorption, and X-ray photoelectron spectroscopy were the characterization techniques employed to confirm the successful functionalization of CNTs as well as the type of interaction existing with the FePcS. All results obtained led to the same conclusion: There were no specific chemical interactions between CNTs and the fixed FePcS.

N-doped carbon xerogels were obtained from organic xerogels prepared using different N-containing organic compounds, including 3-hydroxy aniline, melamine, and 3-hydroxy pyridine. Carbonization was carried out between 500 and 900 degreeC. The surface chemistry of samples was determined by elemental analysis and X-ray photoelectron spectroscopy, their porous texture was determined by N2 and CO2 adsorption at (-)196 and 0degreeC, respectively, and their morphology was determined by scanning electron microscopy. N-doped carbon xerogels with a wide variety of N contents and functionalities were obtained according to the ingredients and carbonization temperature used. Carbon xerogels contained, in different proportions, three/four N functionalities: pyridinic, pyrrolic and/or pyridonic, and quaternary N functionalities. They were microporous carbons with narrow micropores that had constrictions at their entrances, producing higher CO2(-) than N2-determined micropore surface areas. Morphology studies showed samples to be constituted by isolated microspheres or microsphere clusters. Microsphere diameters depended on the recipe and carbonization temperature used.

Acetone solutions of [Au(OClO3)(PCy3)] react with complexes [M{S2C=(t-Bu-fy)}2]2- [t-Bu-fy=2,7-di-tert-butylfluoren-9-ylidene; M=Pd (2a), Pt (2b)] or [M{S2C=(t-Bu-fy)}(dbbpy)] [dbbpy=4,4'-di-tert-butyl-2,2'-bipyridyl; M=Pd (3a), Pt (3b)] to give the heteronuclear complexes [M{S2C=(t-Bu-fy)}2{Au(PCy3)}2] [2:1 molar ratio; M=Pd (4a), Pt (4b)], [M{S2C=(t-Bu-fy)}(dbbpy){Au(PCy3)}]ClO4 [1:1 molar ratio; M=Pd (5a), Pt (5b)], or [M{S2C=(t-Bu-fy)}(dbbpy){Au(PCy3)}2](ClO4)2 [2:1 molar ratio; M=Pd (6a), Pt (6b)]. The crystal structures of 3a, 4a, 4b, 5b, and 6a have been solved by single-crystal X-ray studies and, in the cases of the heteronuclear derivatives, reveal the formation of short Pd...Au or Pt...Au metallophilic contacts in the range of 3.048-3.311 A. Compounds 4a and b and 5a and b undergo a dynamic process in solution that involves the migration of the [Au(PCy3)]+ units between the sulfur atoms of the dithiolato ligands. The coordination of 2a and b and 3a and b to [Au(PCy3)]+ units results in important modifications of their photophysical properties. The dominant effect in the absorption spectra is an increase in the energy of the MLCT (4a and b) or charge transfer to diimine (5a, b, 6a, b) transitions because of a decrease in the energies of the mixed metal/dithiolate HOMOs. The Pd complexes 2a and 4a are luminescent at 77 K, and the features of their emissions are consistent with an essentially metal-centered 3d-d state. The Pt/Au complexes are also luminescent at 77 K, and their emissions can be assigned as originating from a MLCT triplet state (4b) or a mixture of charge transfer to diimine and diimine intraligand pi-pi* triplet states (5b and 6b).

Platinum(II) complexes with (fluoren-9-ylidene)methanedithiolato and its 2,7-di-tert-butyl- and 2,7-dimethoxy-substituted analogues were obtained by reacting different chloroplatinum(II) precursors with the piperidinium dithioates (pipH)[(2,7-R2C12H6)CHCS2] [R = H (1a), t-Bu (1b), or OMe (1c)] in the presence of piperidine. The anionic complexes Q2[Pt{S(2)C=C(C12H6R(2)-2,7)}2] [R = H, (Pr(4)N)(2)2a; R = t-Bu, (Pr4N)(2)2b, (Et4N)(2)2b; R = OMe, (Pr4N)(2)2c] were prepared from PtCl(2), piperidine, the corresponding QCl salt, and 1a-c in molar ratio 1:2:2:2. In the absence of QCl, the complexes (pipH)(2)2b and [Pt(pip)(4)]2b were isolated depending on the PtCl(2):pip molar ratio. The neutral complexes [Pt{S2C=C(C12H6R(2)-2,7)L(2)] [L = PPh(3), R = H (3a), t-Bu (3b), OMe (3c); L = PEt(3), R = H (4a), t-Bu (4b), OMe (4c); L(2) = dbbpy, R = H (5a), t-Bu (5b), OMe (5c) (dbbpy = 4,4'-di-tert-butyl-2,2'-bipyridyl)] were similarly prepared from the corresponding precursors [PtCl2L2] and 1a-c in the presence of piperidine. Oxidation of Q(2)2b with [FeCp2]PF6 afforded the mixed Pt(II)-Pt(IV) complex Q2[Pt2{S2C=C[C12H6(t-Bu)(2)-2,7]}4] (Q(2)6, Q = Et4N+, Pr4N+). The protonation of (Pr4N)(2)2b with 2 equiv of triflic acid gave the neutral dithioato complex [Pt2{S2CCH[C12H6(t-Bu)(2)-2,7]}4] (7). The same reaction in 1:1 molar ratio gave the mixed dithiolato/dithioato complex Pr4N[Pt{S2C=C[C12H6(t-Bu)(2)-2,7]}{S2CCH[C12H6(t-Bu)(2)-2,7]}] (Pr(4)N8) while the corresponding DMANH+ salt was obtained by treating 7 with 2 equiv of 1,8-bis(dimethylamino)naphthalene (DMAN). The crystal structures of 3b and 5c.CH2Cl2 have been solved by X-ray crystallography. All the platinum complexes are photoluminescent at 77 K in CH2Cl2 or KBr matrix, except for Q(2)6. Compounds 5a-c and Q8 show room-temperature luminescence in fluid solution. The electronic absorption and emission spectra of the dithiolato complexes reveal charge-transfer absorption and emission energies which are significantly lower than those of analogous platinum complexes with previously described 1,1-ethylenedithiolato ligands and in most cases compare well to those of 1,2-dithiolene complexes.