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This paper aims to synthesize new benzimidazole dyes aiming to study the solvent effects on their absorption in Ultraviolet-visible spectra.

Ureido/thioureido hydrazonamide benzimidazoles (U/THB) are prepared by condensation of N-aryl-1H-benzo[d]imidazole-2-carbohydrazonoyl bromides with ureido and/ or thioureido reagents. The target products are fully characterized for structural elucidation by means of their spectral and elemental methods. Solvatochromic behavior of U/THB dyes has been studied in different polar protic solvents at room temperature.

The absorption spectra distinguish two main bands at (350 nm–442 nm) and (308 nm–382 nm) referring to n-π* and π- π* transitions of the azo groups. Dimethyl formamide induces an extremely bathochromic transition comparing to the other protic solvents. The observed bathochromic shifts indicate strong interaction with solvents in the excited state. Most dyes show one absorbance in all solvents used, so they may exist in a single tautomeric form (hydrazo form).

In the present paper, the synthesis of U/THB dyes was achieved by a simple and convenient pathway. In addition, the variations in substituents attached to the chromophoric moiety could also be studied.

The new U/THB dyes are accountable for providing good knowledge about their solvation and spectral properties of an order acceptable for industrial utilization.

Synthesis of these new benzimidazole derivatives and study of their solvation and spectral properties provides good knowledge, which is very useful in many industrial applications (e.g. dye-sensitized solar cell, etc.).

The synthesized mono azo U/THB dyes are novel members in the benzimidazole family, where no details regarding the synthesis of such dyes are reported before in the literature. They are superior in terms of preparation, multiple applications and spectral properties.

This paper aims to evaluate the corrosion inhibition capacities of synthesized compounds 1-(2-pyridinyl)-2-(o, m-, p-hydroxyphenyl) benzimidazoles in API 5L X52 steel/HCl 1M corrosion system.

Electrochemical impedance spectroscopy technique was used.

The studies determined that under stagnant conditions, the durability and efficiency were maintained over 80 per cent for up to 500 h of immersion, while the residence time started to decrease after 150 h at the best inhibitor concentration (150 ppm).

This work may help to attenuate corrosion problems in the petroleum industry.

It is the first time that 1-(2-pyridiniy)-2-(o-, m-, p-hydroxyphenyl) benzimidazoles were evaluated as corrosion inhibitors.

The effect of benzimidazole‐2‐tione and benzoxazole‐2‐tione derivatives on the corrosion of aluminium in 0.1 M HCl has been investigated by a potentiostatic polarisation technique. Inhibition efficiencies were found to follow the order: benzimidazole‐2‐tione > 5‐methyl benzimidazole‐2‐tione > 5‐chloro benzimidazole‐2‐tione, while that of benzoxazole‐2‐tione derivatives were found to follow the order: 5‐methyl benzoxazole‐2‐tione > benzoxazole‐2‐tione > 5‐chloro benzoxazole‐2‐tione > 5‐nitro benzoxazole‐2‐tione. The inhibitive action of these heterocyclic compounds was mainly due to adsorption on the metal surfaces, which show parallelism with the calculated total negative charge of each of the molecules. Thermodynamic parameters, such as values of free energies of adsorption ΔG_ads and values of equilibrium constants K_ads, were determined. Activation energies E_a, activation enthalpies ΔH* and activation entropies ΔS* were determined from the corrosion currents measured at different temperatures.

Since Victor Meyer's first report on coupling of diazonium salts with activated carbon compounds, a growing interest has appeared in literature for synthesis and use of different isolated and/or fused nitrogen‐containing heterocyclic dyestuffs as fluorescent whitening agents. A technically important class of these products is those embodying pyrido (1,2‐a) benzimidazole residue in their structure. The parent pyrido (1, 2‐a) benzi‐midazole itself has been previously used in the synthesis of a variety of dyes and pigments.

The influence of N‐heterocyclics, viz. imidazole (IA), benzimidazole (BIA) and 2‐methyl imidazole (MIA) on the corrosion and hydrogen permeation through mild steel in 1 N H₂SO₄ and in 1N HC1 has been studied using weight loss and various corrosion monitoring techniques. Imidazole and benzimidazole inhibit the corrosion of mild steel in both the acidic solutions, but methyl imidazole accelerates the corrosion. They behave as cathodic inhibitors by influencing the cathodic polarization reaction. Except methyl imidazole, the other two compounds reduce the hydrogen permeation current in both the acids. The adsorption of these compounds on the mild steel surface from both the acids obeys Temkin’s adsorption isotherm. Trends in the increase of charge transfer resistance and decrease of capacitance values also show the adsorption of inhibitors on the metal surface.

This paper aims to reduce environment pollution caused by benzotriazole. The authors chose one of the best inhibitors from 2-aminobenzimidazole, 2-methylbenzimidazol, 2-mercaptobenzimidazole and benzimidazole in combination with benzotriazole.

The electrochemical measurement indicated that 2-methylbenzimidazol had the best inhibition behavior. Then, it was mixed with benzotriazole. Techniques such as field emission scanning electron microscopy, atomic force microscopy, Raman spectroscopy and optical contact angle measurements were used.

The results showed that the inhibition efficiency was up to 99.98%, when the mixture concentration was 20 mmol/L and the molar ratio 1:1.

1-benzotriazole was mixed with 2-methylbenzimidazol for the first time. During the exist of methyl, 2-methylbenzimidazol has the better inhibition; this point was ignored by researchers.

The purpose of this paper is to examine the role of tacit knowledge in incremental innovation, which has hitherto been neglected.

Qualitative case analysis was used to focus on two large Japanese pharmaceutical companies’ development of new antihypertensive drugs. The study uses interview data and documentary research materials to explore the knowledge bases of the companies’ research teams as they refined an existing drug to produce new products – a process of incremental innovation.

Explicit knowledge (chemical structure of preceding drug) was used in both successful and failed cases of drug discovery. In the two successful cases, the tacit knowledge of key researchers, based on their long-term experience of related research, provided insight into developing compounds with good in vivo efficacy, which led to successful clinical development.

The findings suggest that tacit knowledge may play an important role in incremental innovation processes, and that its influence on product development should be considered in such ways as team and organization structure.

This study addresses a gap in the literature regarding the impact of tacit knowledge on incremental innovation processes. It is often assumed that incremental innovation is based on existing technology. This study suggests that tacit knowledge may play a hitherto largely unrecognized role in incremental product development.

Some of the azoles have been studied as inhibitors towards the corrosion of nickel in 4% HNO3 solution, using electrochemical polarization technique, at various concentrations of inhibitors and at different temperatures (25, 35, 45°C). All the inhibitors investigated were able to suppress both the anodic and cathodic processes appreciably, hence act as mixed inhibitors. Among these inhibitors, 2‐mercaptobenzothiazole was found to be the most effective inhibitor to control the corrosion of nickel in nitric acid solution.

The purpose of this paper is investigate the inhibition efficiency of three similar bi-cyclic organic compounds, namely, benzimidazole (BI), benzotriazole (BTAH) and benzothiazole (BTH) on carbon steel in 1 M hydrochloric acid (HCl) solution. Organic inhibitors are widely used to protect metals in acidic media. Among abundant suggestions for acid corrosion inhibitors, azole compounds have gained attention.

The inhibition efficiency of the three organic compounds was investigated using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS).

Superiorities of BTH and BTAH corrosion inhibitors were shown by EIS data and polarization curves. Moreover, the results revealed that BTAH and BTH can function as effective mixed-type adsorptive inhibitors, whereas no inhibition behavior was observed for BI. Both BTAH and BTH obeyed Longmuir adsorption isotherm. The results obtained from this isotherm showed that both inhibitors adsorbed on the specimen surface physically and chemically. The difference in inhibition efficiencies of BTAH, BTH and BI was related to the presence of nitrogen and sulfur hetero atoms on their molecular structures.

This study evaluated inhibition efficiency of BI, BTAH and BTH using electrochemical methods. In addition, the study attempted to find inhibition mechanism of the inhibitors and to find modes of adsorption of the inhibitors, correlating effects of heteroatoms and inhibition efficiency.

The emergence of new interconnection technologies involving double‐sided surface mounted components has put stronger restrictions on the method of preserving the solderable finish on printed circuit (PC) boards. The popular Sn/Pb coatings have come under strong scrutiny due to environmental hazards of lead and also because they do not provide flat, planar surfaces for SM assembly. Organic solderability preservative coatings (OSP) are emerging as strong contenders for replacing Sn/Pb surface finishes. Benzotriazole based organic coatings have been successfully used in the past by several electronics manufacturers. However, assembly technologies involving multiple thermal operations have necessitated a fundamental understanding of the thermal stabilities and the mechanism of corrosion protection provided by the OSPs. This paper reports the results of an investigation of the thermal stabilities of two organic corrosion protection coatings. Although both are organic azole based, they operate in two distinct regimes: one forming thin films (∼100 Å) and the other forming thick films (∼5000 Å). The mechanism of surface protection has been studied using direct surface analytical techniques such as X‐ray photoelectron spectroscopy (XPS), Auger electron spectroscopy (AES), scanning transmission electron microscopy (SEM/TEM) and Fourier transform infrared spectroscopy (FT‐IR). The solderability of the copper was measured by wetting balance techniques and correlated to the amount of copper oxidation. The results indicate that, although the thin films provide excellent protection for storage and handling operations, they decompose under heat, thereby causing oxidation of the copper. The thick films appear to withstand multiple thermal cycling. However, the underlying copper substrate can still be oxidised by oxygen diffusion through pores or cracks, or the film may undergo chemical changes that render the copper unsolderable.