Influence of acid treatment on structure of clinoptilolite tuff and its adsorption of methane

This study presents the results of the methane adsorption properties of clinoptilolite tuff from Bigadic, Turkey and that of acid treated forms at 273 and 293 K up to 100 kPa using volumetric apparatus. In order to assess changes in structural and gas adsorption properties of clinoptilolite, zeolite sample was treated with acid solutions of varying concentrations (0.1, 0.5, 1.0 and 2.0 M) at 70 °C during 3 h. Structural and thermal characterization of natural and acid treated clinoptilolite samples were carried out using a combination of techniques such as X-ray diffraction, X-ray fluorescence, thermogravimetric, differential thermal analysis and nitrogen adsorption methods. At both temperatures, uptake of methane (CH₄) increased in the following order: CLN < CLN-H2 < CLN-H1 < CLN-H05 < CLN-H01. CH₄ adsorption capacities of the original and acid treated clinoptilolites were found in the range of 0.476–0.910 mmol/g and 0.398–0.691 mmol/g at 273 and 293 K, respectively.     

Paper conservation methods: a literature review

The main paper conservation methods are presented, classified in the following categories: preparation of the intervention, disinfestation and disinfection/sterilization, surface/dry cleaning, wet cleaning, chemical stabilization, paper repairs, consolidation and strengthening. Treatment documentation is also discussed. The targets, the historical aspects, the general principles, the materials and equipment, the acceptance and criticism pertaining to each method are briefly reviewed, and the most important research for their evaluation is presented. Several paper stabilization strategies, such as deacidification and iron gall ink stabilization, applicable to paper are elucidated. Specific consolidation and strengthening methods for paper, such as lamination and paper splitting are also discussed. The review mainly focuses on the established methods, but experimental, abandoned or insufficiently documented methods are also included. Shortcomings and limitations of several methods were found in the literature, concerning health issues, limited effectiveness, adverse side-effects on the treated artefacts and restricted applicability.     

Ambazone salt with p-aminobenzoic acid

In this study, we obtained a novel salt of ambazone (AMB) with p-aminobenzoic acid (PABA) that exhibits improved solubility and antibacterial activity. The salt was produced by solvent-drop grinding and characterized by powder X-ray diffraction, thermal analysis and Fourier transform infrared spectroscopy. The salt nature of the new form was confirmed by infrared spectroscopy based on the characteristic vibrational band of the protonated amino group. Based on the X-ray powder diffraction data, the compound crystallizes in the triclinic P_-1 space group with the following unit cell parameters: a = 14.294 Å, b = 9.162 Å, c = 8.777 Å, α = 95.90°, β = 100.63°, γ = 91.73°. Thermal analysis reveals the thermal events and different decomposition steps of this solid form as compared to the starting compounds. Powder dissolution measurements showed solubility improvement compared with pure ambazone of 2 and 3.3 times in water and phosphate buffer, respectively. Antibacterial tests showed higher activity of the salt to Gram-negative Escherichia coli and Salmonella bacteria as compared to AMB and PABA. The study demonstrates that the pharmaceutical salt of ambazone with p-aminobenzoic acid (AMB–PABA) can be a possible alternative to ambazone in the treatment of infections with Gram-negative bacteria.     

Selective synthesis of copper microsheets and ultralong microwires via a surfactant assisted hydrothermal process

The surfactant assisted hydrothermal process for selective preparation of copper nanosheets and ultralong microwires by reducing Cu²⁺ with 2-(bis-phosphonomethylamino)propionic acid (dpc) under the action of cetyltrimethylammonium bromide (CTAB) or polyvinyl pyrrolidine (PVP) is presented. X-ray powder diffraction (XRD) and energy dispersive X-ray analysis (EDX) indicate that the products are pure Cu of cubic phase. The effects of starting material concentration and reaction time on morphology of nanosheets have been studied by scanning electron microscopy (SEM). The presence of CTAB and PVP as capping agents is identified by EDX, transmission electron microscopy (TEM) and FT-IR. The possible growth process for ultralong microwires was studied by stopping the growth at a series of intermediate morphology stages based on SEM observations. Optical properties of Cu nanosheets and ultralong microwires were studied by UV-Vis spectrophotometry.     

Synthesis and characterization of nano Ag end capped L-cysteine bridged diblock copolymer

The target of the present investigation is synthesis and characterization of an amphiphilic diblock copolymer with antibacterial property. Ring opening polymerization (ROP) of ε-caprolactone (CL) and tetrahydrofuran (THF) was carried out under inert atmosphere by using L-cysteine as a bridging agent in the presence of stannous octoate (SO) as a catalyst. The nano silver end capped diblock copolymer was synthesized by in situ method. Thus obtained nano silver end capped L-cysteine bridged diblock copolymer was characterized by various analytical methods like Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, circular dichroism (CD), fluorescence spectroscopy, gel permeation chromatography (GPC), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), field emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM) and zeta potential. The antimicrobial property of the nano silver end capped diblock copolymer against e-coli was tested.     

Spectroscopic and structural characterization of pure and FeCl<Subscript>3</Subscript>-containing tri-<Emphasis Type="Italic">n</Emphasis>-butyl phosphate

The spectroscopic properties and liquid structure of pure tri-n-butyl phosphate (TBP) and FeCl₃/TBP solutions have been investigated by Uv–Vis and Raman spectroscopies, X-ray diffraction and conductometry. Uv–Vis and Raman spectra, supported by conductometric measurements, consistently indicate that the solubilized salt is present mostly as TBP _n [FeCl_3???n ] ⁿ⁺ and FeCl₄ ^? complex ions due to specific interaction with the TBP phosphate group. Thanks to this interaction, a high amount of salt (up to 13 % w/w) can be dissolved despite the relatively low dielectric constant of TBP. The X-ray diffractogram of pure TBP has been interpreted in terms of three main contributions which can be attributed to spatial pair correlations between atoms of interacting TBP molecules. In the presence of increasing FeCl₃ amounts, it has been observed a progressive structuring effect, exerted by the dissolved salt, on the layers of opportunely oriented TBP molecules due to the formation of the complex ionic species. By simple treatment with NaBH₄, the synthesis of Fe nanoparticles has been achieved. The absence of water, the easiness of preparation, the high amount of salt which can be suspended and the peculiar physico-chemical properties of such systems are all elements worth of note for the fields of nanoparticle synthesis and for specialized technological applications.     

Thermo- and pH-responsive fluorescence behaviors of sulfur-functionalized detonation nanodiamond-poly(<Emphasis Type="Italic">N</Emphasis>-isopropylacrylamide)

Detonation nanodiamonds (DNDs) are emerging as bioimaging platforms due to their biocompability, small primary particle size, reactive surface, and stable fluorescence after modification. In this paper, a heteroatom engineering method is provided to fabricate the fluorescent DNDs through pyrolysis of dibenzyl disulfide. The quantum yield of these sulfur (S)-functionalized DNDs (SDNDs) increases with sulfur percentage. The solubility and stability of SDNDs in aqueous solution are also significantly increased due to the formation of hydrophilic sulfur groups on DND. Furthermore, these SDNDs are used to conjugate the stimuli-responsive poly(N-isopropylacrylamide) (PNIPAM) through the ‘graft from’ method. The conjugation demonstrated both pH- and thermo-responsive fluorescence behaviors, which shows promise to be used in ratiometric fluorescence sensing for the detection of intracellular pH and temperature values.     

A closed form solution for the vulcanization prediction of NR cured with sulphur and different accelerators

The paper presents a novel efficient closed form approach to determine the degree of vulcanization of natural rubber (NR) vulcanized with sulphur in presence of different accelerators. The general reaction scheme proposed by Han and co-workers for vulcanized sulphur NR is re-adapted and suitably modified taking into account the single contributions of the different accelerators, focusing in particular on some experimental data, where NR was vulcanized at different temperatures (from 150 to \(180\, ^{\circ }\hbox {C}\)) and concentrations of sulphur, using TBBS and DPG in the mixture as co-agents at variable concentrations. In the model, chain reactions initiated by the formation of macro-compounds responsible for the formation of the unmatured crosslinked polymer are accounted for. It is assumed that such reactions depend on the reciprocal concentrations of all components and their chemical nature. In presence of two accelerators, reactions are assumed to proceed in parallel, making the assumption that there is no interaction between the two accelerators. Despite there is experimental evidence that a weak process by which each accelerator affects the other, the reaction chemistry is still not well understood and therefore its effect cannot be translated into any mathematical model. In any case, even disregarding such interaction, good approximations of the rheometer curves are obtained. From the simplified kinetic scheme adopted, a closed form solution is found for the crosslink density, with the only limitation that the induction period is excluded from computations. The main capability of the model stands however in the closed form determination of kinetic constants representing the velocities of single reactions in the kinetic scheme adopted, which allows avoiding a numerically demanding least-squares best fitting on rheometer experimental data. Two series of experiments available, relying into rheometer curves at different temperatures and different concentrations of sulphur and accelerators, are utilized to evaluate the fitting capabilities of the mathematical model. Very good agreement between numerical output and experimental data is experienced in all cases analyzed.     

Mononuclear transition and non-transition complexes of amlodipine besylate as antihypertensive agent: synthesis,spectral, thermal,and antimicrobial studies

Mononuclear Mn(II), Co(II), Ni(II), Zn(II), Cd(II), Mg(II), Sr(II), Ba(II), Ca(II), Pt(IV), Au(III), and Pd(II) complexes of the drug amlodipine besylate (HL) have been synthesized and characterized by elemental analysis, spectroscopic technique (IR, UV–Vis, solid reflectance, scanning electron microscopy, X-ray powder diffraction, and ¹H-NMR) and magnetic measurements. The elemental analyses of the complexes are confirmed by the stoichiometry of the types [M(HL)(X)₂(H₂O)]·nH₂O [M = Mn(II), Co(II), Zn(II), Ni(II), Mg(II), Sr(II), Ba(II), and Ca(II); X = Cl^? or NO₃ ^?], [Cd(HL)(H₂O)]Cl₂, [Pd(HL)₂]Cl₂, [Pt(L)₂]Cl₂, and [Au(L)₂]Cl, respectively. Infrared data revealed that the amlodipine besylate drug ligand chelated as monobasic tridentate through NH₂, oxygen (ether), and OH of besylate groups in Mn(II), Co(II), Ni(II), Zn(II), Cd(II), Mg(II), Sr(II), Ba(II), Ca(II), and Au(III) complexes, but in Pt(IV) and Pd(II) complexes, the amlodipine besylate coordinates via NH₂ and OH (besylate) groups. An octahedral geometry is proposed for all complexes except for the Cd(II), Pt(IV), and Pd(II) complexes. The amlodipine besylate free ligand and the transition and non-transition complexes showed antibacterial activity towards some Gram-positive and Gram-negative bacteria and the fungi (Aspergillus flavus and Candida albicans).