Search

In the manufacturing of optical products, precise adjustments are made to maintain the optical axis alignment of optical components, which are then securely positioned using adhesives. To achieve positional accuracy at the micron level, it is essential to comprehend the deformation of the adhesive joint over time during processing. This study focuses on investigating the displacement of optical components resulting from the deformation of a cationic photopolymerized epoxy adhesive, which cures under ultraviolet (UV) radiation. First, the conversion of the adhesive was formulated based on a curing reaction model. This conversion can be divided into three stages: the initial reaction during UV irradiation, the subsequent dark reaction, and the reaction induced by heating. Moreover, formulations were developed to describe changes in curing shrinkage, thermal expansion, and viscoelasticity in relation to the conversion. These equations, governing the adhesive properties, were then used to perform finite element method (FEM) simulations to analyze the position of the optical component. Experimental tests on adhesively bonded components were conducted under conditions identical to those employed in the simulation. Throughout the curing process of the adhesive, the optical component was continuously imaged using a coherence-scanning interferometer, enabling the quantification of its displacement from the acquired images. The results of the FEM simulation and experimental analysis exhibited a consistent trend, indicating the effectiveness of the modeling and simulation methods employed in this study. The majority of the displacement of the optical component occurred over several hours during the dark reaction stage, rather than during UV irradiation. Notably, the movement of the optical component was not limited solely to the thickness direction of the adhesive layer because of curing shrinkage but also extends to the in-plane direction because of the non-uniform distribution of the UV irradiation intensity. [ABSTRACT FROM AUTHOR]

In photosynthetic bacteria, light-induced electron transfer takes place in a protein called the reaction center (RC) leading to the reduction of a bound ubiquinone molecule, QB, coupled with proton binding from solution. We used electron paramagnetic resonance (EPR) and electron-nuclear double resonance (ENDOR) to study the magnetic properties of the protonated semiquinone, an intermediate proposed to play a role in proton coupled electron transfer to QB. To stabilize the protonated semiquinone state, we used a ubiquinone derivative, rhodoquinone, which as a semiquinone is more easily protonated than ubisemiquinone. To reduce this low-potential quinone we used mutant RCs modified to directly reduce the quinone in the QB site via B-branch electron transfer (Paddock et al. in Biochemistry 44:6920–6928, 2005). EPR and ENDOR signals were observed upon illumination of mutant RCs in the presence of rhodoquinone. The EPR signals had g values characteristic of rhodosemiquinone (g x  = 2.0057, g y  = 2.0048, g z  ~ 2.0018) at pH 9.5 and were changed at pH 4.5. The ENDOR spectrum showed couplings due to solvent exchangeable protons typical of hydrogen bonds similar to, but different from, those found for ubisemiquinone. This approach should be useful in future magnetic resonance studies of the protonated semiquinone.