Preparation of Internally Plasticized Ester of Cellulose Irradiated by Microwave and Its Properties

This paper demonstrates esterification of cellulose with long-chain carboxylic acid in a homogeneous phase irradiated by microwave. The esterification reaction system was cellulose, fatty acid, and LiCl/dimethylacetamide (LiCl/DMAc) using p-toluenesulfonyl chloride (Ts-Cl) as activating reagents. It was found that the use of a microwave resulted in a dramatic drop in reaction time (90s), two orders of magnitude faster than conventional reaction under heating. The degrees of substitution (DS) and molar yields of fatty acid, Ts-Cl amounts and reaction time, as well as the property of final products, were studied. Partially derivative celluloses, which underwent a significant change in morphological structure during the modification, presented obvious glass transition compared to starting cellulose. In agreement with this, the crystallization property of the internally plasticized esters was different from cellulose. Together, these results indicated the reaction of acylation.     

Development of a Compact and User-friendly Ion Irradiation System Controlled Remotely through the Internet

A compact and user-friendly ion irradiation system controlled remotely through the Internet was developed for the execution of collaboration experiments together with researchers at remote sites. Several hardware instruments and software programs were constructed and provided for the remote control of the system and for its connection to the Internet. Surface modification and analysis experiments with this system were remotely performed through the Internet. It was confirmed from the experiments that the present ion irradiation system was precisely controlled through the Internet and could be easily and safely used for the surface modification and analysis, that the normal communication speed of around 10Mbps for the Internet was fast enough for the execution of such typical remote-controlled experiments, and also that an access to the system by a mobile phone was convenient and useful enough to check the condition of the system and experimental data.     

Effect of Ni7+ Ion Irradiation on Structure and Ammonia Sensing Properties of Thermally Oxidized Zinc and Indium Films

ZnO and In2O3 films were prepared by thermal oxidation of vacuum deposited zinc and indium films, respectively onto the glass substrate at 30 C. The fabricated films have been irradiated with 100-MeV Ni7+ ions at different fluences ranging from 5×1011 to 5×1013 ions/cm2. The structural and gas sensing properties of pristine and irradiated films have been discussed. X-ray diffraction (XRD) pattern of pristine and irradiated films reveal that the films are polycrystalline in nature and crystallinity increases after irradiation. In this study, highly porous In2O3 nanorods evolved when being irradiated at a fluence of 5×1013 ions/cm2 while ZnO film shows decrease in number of nanowires. The ammonia sensing performance of the Ni7+ irradiated In2O3 films shows an improvement as compared to its pristine counterpart.     

A chemically amplified molecular glass resist with an ionic photoacid generator and a single protection group

A molecular glass resist with an ionic photoacid generator and a single protection group (MR‐1) has been developed. MR‐1 exhibited good thermal properties, such as a 5% weight loss temperature (T_d5%) of 167°C and a glass transition temperature (T_g) of 80°C. MR‐1 showed the good sensitivity of 80 μC/cm² and high contrast of 4.9 with e‐beam exposure (50 keV). A relatively high resolution of 50 nm and low Line‐Edge‐Roughness of 3.8 nm were obtained by e‐beam exposure (100 keV). © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39769.     

PET包装材料中紫外吸收剂迁移研究进展

PET包装材料广泛应用于食品包装中,为了提高对应的抗光氧化能力,会添加一定量的紫外吸收剂于其中,而紫外吸收剂在长期贮存过程中存在迁移溶出隐患。对PET包装材料中紫外吸收剂的种类、迁移机制及国内外迁移研究进展进行综述,并进行展望。     

Near tip stress intensity factor for an edge-crack in a Pb(ZrxTi1−x)O3 thin film with 90° domain switching under a continuous laser irradiation

The near tip stress intensity factor K_Itip for an edge-crack in a Pb(Zr_xTi_1−x)O₃ thin film was investigated by superposition of the applied stress intensity factor K_Iapp under a continuous laser irradiation and the shielding stress intensity factor ΔK_I for 90° domain switching. Both K_Iapp and ΔK_I were solved by the weight function method, and switching toughening was analyzed based on the small scale domain switching theory. Results show that K_Itip of the edge-crack in the thin film is significantly affected by the initial poling angle, and the edge-crack tip is toughened by the domain switching area with the increase of the initial poling angle. The methodology can predict the fracture toughening of Pb(Zr_xTi_1−x)O₃ thin films quantitatively.     

微波相转移催化快速合成苯甲酸

在相转移催化剂存在下 ,使用微波辐射快速合成了苯甲酸。该方法反应条件温和、操作简便 ,反应 1 5 min产率可达 85 % ,后处理不用脱色和重结晶就能得到白色的苯甲酸晶体。     

Photopolymerizable liquid encapsulants for microelectronic devices: Thermal and mechanical properties of systems with reduced in‐mold cure times

Photopolymerizable liquid encapsulants (PLEs) for microelectronic devices may offer important advantages over traditional transfer molding compounds, including reduced in‐mold cure times, lower thermal stresses, and reduced wire sweep. In this contribution, we discuss an encapsulation process based upon a low viscosity resin that cures rapidly upon exposure to UV light. These highly filled PLEs are comprised of an epoxy novolac‐based vinyl ester resin (～25 wt %), fused silica filler (70–74 wt %), photoinitiator, silane coupling agent, and, in some cases, a thermal initiator. We have characterized the material properties (flexural strength and modulus, coefficient of thermal expansion, glass transition temperature, and thermal stress parameter) of PLEs cured with UV illumination times of 60, 90, and 120 s, as well as, the thermal conductivity and adhesive peel strength of PLEs photocured for 90 s. In addition, we investigated the effect of the fused silica loading and the initiation scheme on these properties. The results indicate that the PLEs are very promising for microelectronic encapsulation. These liquid encapsulants cure (to an ejectable hardness) in 1 min for an initiating light intensity of 200 mW/cm², and exhibit appropriate values for the thermal and mechanical properties listed above. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 3449–3461, 2001     

Functionalization of Polymer Surfaces Using Excimer VUV Systems and Silent Discharges. Application to Electroless Metallization

New approaches for electroless plating of nonconductive polymers or polymer-based materials are described. In this work, polyimide substrates were surface-functionalized (i) in nitrogenated (ammonia at reduced pressure) and oxygenated (air at atmospheric pressure) atmospheres under assistance of vacuum-ultraviolet (VUV) irradiation (use of a xenon silent discharge excimer source) or (ii) directly in air at atmospheric pressure using a dielectric-barrier discharge (DBD) device. After functionalization, the substrates were “activated” by dipping in a dilute acidic PdCl₂ solution or by spin-coating of a thin metal-organic film (from a solution of palladium acetate (PdAc) in chloroform). The catalytic activity of the so-deposited palladium species toward the electroless deposition of nickel was studied before and after a VUV post-irradiation (in air at atmospheric or reduced pressure) with a view to understanding better the role of the reducer (sodium hypophosphite) within the electroless bath.

This work confirms the specific interest of grafting nitrogenated functionalities onto polymer surfaces for attaching covalently the palladium-based catalyst (in particular in the case of the PdCl₂ route), forming thus strong Pd - N - C bonds at the metal/polymer interface. This results from the strong chemical affinity of palladium toward nitrogen. On the other hand, when oxygenated functionalities are surface-grafted, the conventional two-step procedure using SnCl₂ and PdCl₂ solutions can be proposed due to the strong chemical affinity of tin toward oxygen. The Ni deposits obtained under these different conditions pass the standard Scotch^®-tape test and, therefore, exhibit a good practical adhesion. For this same purpose, it is interesting to note that the DBD treatment operating in air at atmospheric pressure causes an increase of the surface roughness and, therefore, an improvement in adhesion of metallic films when their initiation is catalyzed through the PdAc route. In addition, this work demonstrates that extensive research still has to be performed to understand and improve the Ni/polymer adhesion when the PdAc route associated with a VUV irradiation is considered.     

UV nanoimprint using flexible polymer template and substrate

Nano to micro-sized patterns were formed on a flexible polymer substrate using a flexible UV imprint stamp. A 6 in. diameter flexible UV nanoimprint template was fabricated using PVC hot embossing and DLC coating. Using the UV nanoimprint process with the DLC coated PVC template, nano to micro-sized patterns were clearly formed on the flexible PET substrate without a residual layer, due to the antistiction properties and high mechanical hardness of the DLC coating. By depositing a Cr layer on the imprinted resist pattern and lifting it off, Cr metal patterns were fabricated on the PET substrate.