RESUMEN
We investigated the material properties of Cremonese soundboards using a wide range of spectroscopic, microscopic, and chemical techniques. We found similar types of spruce in Cremonese soundboards as in modern instruments, but Cremonese spruces exhibit unnatural elemental compositions and oxidation patterns that suggest artificial manipulation. Combining analytical data and historical information, we may deduce the minerals being added and their potential functions-borax and metal sulfates for fungal suppression, table salt for moisture control, alum for molecular crosslinking, and potash or quicklime for alkaline treatment. The overall purpose may have been wood preservation or acoustic tuning. Hemicellulose fragmentation and altered cellulose nanostructures are observed in heavily treated Stradivari specimens, which show diminished second-harmonic generation signals. Guarneri's practice of crosslinking wood fibers via aluminum coordination may also affect mechanical and acoustic properties. Our data suggest that old masters undertook materials engineering experiments to produce soundboards with unique properties.
RESUMEN
Wood has been a crucial natural material for human civilization since prehistoric times. In archaeology, the examination of the wood microstructure is important for the study of architecture, musical instruments, sculptures, and so on. Scanning electron microscopy (SEM) examination is sometimes unsuitable for archaeological wood due to the limited amount of precious samples, which may be too small to be cut by microtomes and mounted on holders. Moreover, the conductive coating material cannot be uniformly deposited over uneven wood surfaces. To overcome these issues, a rapid and simple pretreatment method using room-temperature ionic liquids (RTIL) was proposed. Four common RTILs were evaluated for the pretreatment of wood chips for SEM examination. We found that water content, viscosity, density, and hydrophobicity of IL solutions were important factors affecting SEM image quality. A 7.5% solution of 1-butyl-1-methylpyrrolidium dicyanamide (BMP-DCA) in ethanol (v/v) was found to work very well. The IL pretreatment could be performed in a few minutes without special equipment. It is gentle enough to preserve delicate structures such as the torus/margo of pit membranes, even at elevated temperatures, without causing obvious damage or deformation. We successfully imaged hand-cut wood chips from 18th-century buildings, an 18th-century European violin, and a Chinese zither over 1000 years old. We therefore conclude that highly hydrophilic ionic liquids with low density and viscosity are suitable for use in SEM examinations of both modern and antique wood specimens.
RESUMEN
A new microfluidic paper-based analytical device, a (Ag-µPAD)-based chemiresistor composed of silver ink, has been developed for the selective, sensitive, and quantitative determination of nitrite ions in environmental analysis. The silver ink acts as an efficient transducer in terms of resistance changes due to nitrite initiating a diazo reaction and further reacting with the ink. The silver ink is synthesized onto the µPADs by pulsed light sintering from silver nanoparticles, a mixture of silver nanowires and nanoparticles. The resistance changes show two linear response ranges to nitrite in the concentration ranges of 1.0 × 10-8 M to 5.0 × 10-6 M and 1.0 × 10-5 M to 3.2 × 10-3 M, with a limit of detection of 8.5 × 10-11 M (S/N = 3). The sensor displays a wider linear range, a lower detection limit, a higher stability, high selectivity, low-volume sampling, and disposability for nitrite with respect to other nanoparticle- and paper-based sensors. The characterization of silver ink was verified by SEM, EDS, and IR studies, and the sensing mechanism is discussed. In addition, this paper-based sensor has been successfully employed to determine the nitrite content in tap, river and lake water samples.
RESUMEN
An entangled composite compound, [Ni4(dpe)4(btc)2(Hbtc)(H2O)9]·3H2O (1), where H3btc = 1,3,5-benzenetricarboxylic acid and dpe = 1,2-bis(4-pyridyl)ethane, has been synthesized and structurally characterized. Single-crystal structural determination reveals that compound 1 consists of four coordination polymers (CPs), with two two-dimensional (2D) (4,4) layered metal-organic frameworks (MOFs) of [Ni(dpe)(Hbtc)(H2O)] and [Ni(dpe)(btc)(H2O)]- anion, and two one-dimensional (1D) polymeric chains of [Ni(dpe)(btc)(H2O)3]- anion and [Ni(dpe)(H2O)4]2+ cation, respectively. The three-dimensional (3D) supramolecular architecture of 1 is constructed via the inter-penetration of inter-digited, double-layered, 2D rectangle-grid MOFs by two 1D coordination polymeric chains, and tightly entangled together via the combination of inter-CPs πâ»π stacking and hydrogen bonding interactions. The ad-/de-sorption isotherms of 1 for water displays a hysteresis profile with a maximum adsorption of 17.66 water molecules of per molecule unit at relative P/P0 < 0.89. The reversible de-/re-hydration processes in 1 monitored by cyclic water de-/ad-sorption TG analysis and PXRD measurements evidence a sponge-like water de-/ad-sorption property associated with a thermal-induced solid-state structural transformation. The magnetic property of 1 suggests that the ferromagnetic coupling might refer to a stronger inter-Ni(II) interaction, which could be along the btc3- or Hbtc2- ligands; the antiferromagnetic coupling corresponding to the weaker inter-Ni(II) interactions, which could be the dpe ligands for the 2D framework.