Aesthetically textured,hard latex coatings by fast IR-assisted evaporative lithography

Polymer coatings with periodic topographic patterns, repeating over millimetre length scales, can be created from lateral flows in an aqueous dispersion of colloidal particles. The flow is driven by differences in evaporation rate across the wet film surface created by IR radiative heating through a shadow mask. This new process, which we call IR radiation-assisted evaporative lithography (IRAEL), combines IR particle sintering with the concept of evaporative lithography. Here, a series of experiments has been conducted in which the mass of the latex is measured as a function of the exposure time under infrared radiation through a mask. The water evaporation rates and the minimum exposure time required for a dry film are estimated as a function of the power density of the IR emitter. The temperature of the wet film is monitored to avoid overheating and boiling of the water, which will otherwise cause defects. It is demonstrated that textured films can be created on a variety of substrates (plastics, metals, paper and glass), and processing times can be as short as 5 min. We use IRAEL to decorate household goods with an aesthetic coating with the desired texture.     

辐射板强化喷管换热与红外抑制效果试验研究

试验研究了在发动机喷管中加装金属辐射板前后,喷管壁面温度、热喷流温度与喷管红外辐射特征的变化。结果表明,加装金属辐射板后,热喷流与喷管壁面之间的热量传递显著增强,热喷流中心温度降低,壁面温度明显升高,在90°方向上,热喷流3～5μm波段的红外辐射强度降低了38.5%。文中从热喷流、喷管壁面以及金属辐射板等相关部件的温度变化情况对红外辐射强度的变化原因进行了解释。      

Experimental and Calculational Studies of the Interactions of BF3 with Fluoroethers

BF₃ was co-condensed with (C₂H₅)₂O, (CF₃CH₂)₂O, and (C₂F₅)₂O in excess argon at 15 K. Infrared spectra of the matrices showed a definite Lewis acid-base interaction between BF₃ and diethyl ether; a weak but definite interaction with bis(2,2,2,-trifluorodiethyl)ether, and no observable interaction with perfluorodiethyl ether. Molecular orbital (MO) calculations complemented the experimental observations by revealing that fluorine atoms on the ethers decreased electron localization about the oxygen atom. Thus, the experimental data and MO calculations indicated a clear trend between strength of interaction with BF₃ and the degree of ether F substitution. The implications of the results for commercial perfluoro ether lubricant/metal oxide surface interactions are discussed.     

Deformation and thermodynamic processes in explosion cladding of cylindrical components with titanium

The structural special features of the formation of titanium in high-speed compression of a titanium pipe are investigated. The thermodynamic conditions of explosion welding of titanium are studied. It is shown that for high-quality cladding of cylindrical components with titanium it is necessary to prevent localization of deformation as a result of heating of the surface and transfer of titanium to the plastic state when welding is carried out in shielding gases. Long copper+titanium current conductors with the length exceeding 30 diameters were produced.     

Thermal and Spectroscopic Analyses of Caustic Side Solvent Extraction Solvent Contacted with 16 Molar and 8 Molar Nitric Acid

Abstract

Thermal and spectroscopic analyses were performed on multiple layers formed when Caustic Side Solvent Extraction (CSSX) solvent was contacted with 16 M or 8 M nitric acid. A rapid (i.e., minutes to hours) chemical reaction occurs between the solvent and 16 M or 8 M nitric acid as evidenced by color changes and the detection of nitro groups in the infrared spectrum of the aged samples. Thermal analysis revealed that decomposition of the resulting mixture does not meet the definition of explosive or deflagrating material.     

Infrasorb: Optical detection of the heat of adsorption for high throughput adsorption screening of porous solids

The demand for fast screening methods in modern materials chemistry led to the development of a room temperature operated high-throughput tool for adsorption screening. Within five minutes a porosity screening of a large sample pool can be realized. Using a variety of different porous materials (activated carbons, porous polymers, metal-organic frameworks, zeolites) and the test gas n-butane, the reliability of the new instrument is shown. Furthermore, possible applications in the determination of n-butane capacities and BET surface areas are given as well as the application in synthesis or product control.The presented data exhibit high quality factors for the correlation of integrated signal intensity (heat of adsorption) and specific surface areas (above 0.97). As an example for the applicability of other gases that can be used with this tool, screening measurements using cyclohexane as test gas are also presented. The developed automated screening tool is an important step to overcome the bottle-neck between high-throughput syntheses technologies developed in the last decades and measurement of adsorption properties.     

Investigation of the phase separation of PNIPAM using infrared spectroscopy together with multivariate data analysis

The use of vibrational spectroscopy to investigate complex structural changes in polymers yields chemically rich data, but interpretation can be challenging and subtle but meaningful spectral changes may be missed through visual inspection alone. Multivariate analysis is an efficient approach to gain an oversight of small but systematic spectral differences anywhere within the spectra, providing further insight into structural changes and associated transformation mechanisms. In this study, the novel analytical approach of infrared spectroscopy combined with principal component analysis and Gaussian peak fitting was used to investigate the structural changes in aqueous solutions of a polymer, using poly(N-isopropyl acrylamide) (PNIPAM) in the atactic form and with controlled tacticity as a model system. Subtle spectral changes associated with the dehydration and phase separation upon heating included peak shifts, an area ratio change of the amide I band to the amide II band and formation of a new peak in the amide I band were efficiently detected. Dehydration and phase separation of PNIPAM occurred in two temperature ranges, one for the atactic and one for isotactic rich part, both involving a complex re-organization of the hydrogen bonds and change of the hydration layer. The changes agreed with existing results from other techniques, and new insights were gained into the effect of controlled tacticity on phase transformation behaviour. The study demonstrates that infrared spectroscopy combined with the multivariate analytical method principal component analysis and Gaussian peak fitting is an efficient approach to probing structural change in polymers during heating. The simplicity of the presented approach could find excellent use in analysing and understanding the molecular environment of a range of stimuli-responsive polymers, for instance block or grafted types of polymers, as well as those with controlled tacticity.     

Adsorption of Alkanethiols on Gold Surfaces: PM-IRRAS Study of the Influence of Terminal Functionality on Alkyl Chain Orientation

The present paper focuses on a simplified method to study the orientation and the anisotropy of two different alkanethiols self-assembled monolayers on gold surfaces. The alkanethiols of interest vary only by their terminal functionalities (COOH and COOCH₃), thus allowing one to highlight the influence of these ending chemical groups on the final orientation of the adsorbed molecules. 11-Mercaptoundecanoic acid [HS-(CH₂)₁₀-COOH] and the methyl-11-mercaptoundecanoate [HS-(CH₂)₁₀-COOCH₃] were grafted under adequate conditions to obtain a high grafting density on gold substrates. These latter, before and after the alkanethiol adsorption, were analyzed mainly by the polarization-modulation infrared reflection-absorption spectroscopy (PM-IRRAS) technique to access orientation angles, and by atomic force microscopy (AFM) to check the homogeneity of the grafted layer.

By applying an original PM-IRRAS simplified method, the results showed an orientation closer to the normal of the surface plane in the case of the acid thiol compared with the ester one, which is probably because of the lateral hydrogen bonds established between the adjacent COOH functions. This method offers a direct and simple way to quantify the orientation angles in the alkanethiol nanofilms.     

Bond Strength of a Silicone Soft Lining Material to Poly(methyl methacrylate) Resin Treated with Maleic Anhydride and its Terpolymers

This study investigated the effectiveness of surface treatment of Poly (methyl methacrylate) (PMMA) denture base resin on tensile bond strength between PMMA/silicone-based soft liner. A total of 25 specimens were fabricated and assigned into five groups (n = 5). The surfaces of PMMA were treated with maleic anhydride, maleic anhydride-styrene-vinyl-acetate, n-butylmaleate-styrene-vinyl-acetate, or n-pentamaleate-styrene-vinyl-acetate prior to Primo adhesive primer application and silicone liner placement. The Primo adhesive primer on applied group untreated dentuse base resin served as control. The tensile test was performed using a universal testing machine. Fractured surfaces were observed under Scanning Electron Microscopy (SEM) and spectroscopic interpretation of the interfaces was done by Fourier Transform Infrared (FTIR). Test results showed that surface treatment increased interfacial strength giving the highest value for n-butylmaleate-styrene-vinyl acetate treated group. SEM micrographs revealed that the specimens with n-butylmaleate-styrene-vinyl-acetate and n-penta maleate-styrene-vinyl-acetate terpolymers underwent cohesive failure. FTIR analysis indicated secondary interactions such as hydrogen bonding, possibly on acrylic resin surfaces, caused by the use of maleic anhydride and its terpolymers, and the adhesive.     

FT-IR SPECTROSCOPY OF NITRIC ACID IN TBP/OCTANE SOLUTION*

Infrared studies for the HNO₃/0.73 M TBP n-octane system are reported. Two extracted species, TBP · HNO₃ and TBP · 2HNO₃, were identified in the organic phase. The concentration of the individual species was determined by the analysis of the vibrational band at ～1650 cm^?1. The band at 1648 cm^?1 was assigned to the monosolvate TBP · HNO₃ and the band at 1672 cm^?1 to the hemisolvate TBP · 2HNO₃. The infrared spectra revealed that with respect to the P═O bond, as well to each other, the HNO₃ molecules in the hemisolvate are spectrally non-equivalent. The predominant structure of TBP · 2HNO₃ involves the chain HNO₃ dimer. Some ionic NO₃ ^? and hydronium ions were identified in this system but only during formation of the monosolvate. The analyses performed in this system can serve for the characterization of HNO₃ in related systems in the presence of metal species.