Current antismudge coatings that bear nano-pools of a grafted liquid ingredient for dewetting enablement (NP-GLIDE) are cured at high temperatures, which are undesirable for application on heat-sensitive substrates. Reported herein is the development of a NP-GLIDE coating that can be photocured at room temperature. Of the various formulations that have been tested, robust coatings were obtained from one recipe consisting of a photoinitiator, a trifunctional monomer that bears three double bonds, and a graft copolymer. The last bears pendent double bonds and a poly(dimethylsiloxane) (PDMS) side chain as the antismudge agent. Coatings were prepared by casting films from a solution containing these three components and then photolyzing the resultant films. A systematic study revealed that the liquid sliding property developed on the coating at a lower cross-linking density than that required for ink to contract. Further, retaining the ability to contract ink traces after many writing and erasing cycles was the most demanding of the three antismudge tests. For our optimized formulation, only 5 min of irradiation was required to yield a transparent coating with superior antismudge properties. Moreover, irradiating selected regions and then removing, with a solvent, reagents in the nonirradiated regions can yield a surface with patterned wettability. These advantageous properties of the new photocurable coating facilitate its applications.

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Sustainable thermal insulating materials produced from cellulosic fibers provide a viable alternative to plastic insulation foams. Industrially available, abundant, and inexpensive mechanical pulp fiber and recycled textile fiber provide potential raw materials to produce thermal insulating materials. To improve the fire retardancy of low-density thermal insulating materials produced from recycled cotton denim and mechanical pulp fibers, bio-based fire retardants, such as sulfonated kraft lignin, kraft lignin, and nanoclays, were coated onto sustainable insulating material surfaces to enhance their fire retardancy. Microfibrillated cellulose was used as a bio-based binder in the coating formula to disperse and bond the fire-retardant particles to the underlying thermal insulating materials. The flammability of the coated thermal insulating materials was tested using a single-flame source test and cone calorimetry. The results showed that sulfonated kraft lignin-coated cellulosic thermal insulating materials had a better fire retardancy compared with that for kraft lignin with a coating weight of 0.8 kg/m2. Nanoclay-coated samples had the best fire retardancy and did not ignite under a heat flux of 25 kW/m2, as shown by cone calorimetry and single-flame source tests, respectively. These cost-efficient and bio-based fire retardants have broad applications for improving fire retardancy of sustainable thermal insulating materials.

For this study, aimed at proposing a potential direction to prevent sulfuric acid dew point corrosion, a Ni–Cr–Mo alloy Hastelloy C22 coating was fabricated by coaxial laser cladding technology. The phase composition, microstructure, and corrosion behavior in a simulated sulfuric acid dew point corrosion environment were investigated and compared with a Hastelloy C22 alloy, a titanium alloy TC4, and 09CrCuSb steel (ND). The results showed that the phase composition of the C22 coating is essentially similar to that of the C22 alloy, consisting of a γ-Ni solid solution and Ni6Mo6C1.06. The finer microstructure of the C22 coating mainly contains eutectic and dentrite, presenting a typical solidification feature of laser cladding. The corrosion resistance of the C22 coating is very close to that of the C22 alloy, and outclasses that of TC4 and ND. The corrosion behavior of the C22 coating is intergranular corrosion resulting from the segregation of molybdenum, chromium containing corrosion products, and smaller anode micro-batteries.

Dissimilar alloys of Ti-6Al-4V and 5A06 Al were butt joined by Al based fillers using a novel TIG welding process, referred to as keyhole arc welding-brazing. The flow behaviour of weld pool was introduced, which was characterised by the formation of a keyhole under the tungsten electrode. It was found that porosity tended to be produced in the middle of the fusion line, while adding elements prevented its formation. At brazing interface, interfacial reaction at root face was enhanced, and a uniform serrated layer, identified as TiAl 3 , was obtained by pure Al fillers. When Al-Cu-La fillers were used, block Ti 2 Al 20 La phases appeared at the interface between the TiAl 3 layer and the brazed seam. Compared to joints brazed by pure Al fillers, the formation of Ti 2 Al 20 La reduced the hardness of the interfacial layer by more than half, while Al 2 Cu increased that of the brazed seam by y50%. The tensile strength of Ti/Al joints reached 270 MPa.

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The mechanism and kinetics of thermal degradation of materials developed from cellulose fiber and synergetic fire retardant or expandable graphite have been investigated using thermogravimetric analysis. The model-free methods such as Kissinger-Akahira-Sunose (KAS), Friedman, and Flynn-Wall-Ozawa (FWO) were applied to measure apparent activation energy (E a). The increased E a indicated a greater thermal stability because of the formation of a thermally stable char, and the decreased E a after the increasing region related to the catalytic reaction of the fire retardants, which revealed that the pyrolysis of fire retardant-containing cellulosic materials through more complex and multi-step kinetics. The Friedman method can be considered as the best method to evaluate the E a of fire-retarded cellulose thermal insulation compared with the KAS and FWO methods. A master-plots method such as the Criado method was used to determine the possible degradation mechanisms. The degradation of cellulose thermal insulation without a fire retardant is governed by a D3 diffusion process when the conversion value is below 0.6, but the materials containing synergetic fire retardant and expandable graphite fire retardant may have a complicated reaction mechanism that fits several proposed theoretical models in different conversion ranges. Gases released during the thermal degradation were identified by pyrolysis-gas chromatography/mass spectrometry. Fire retardants could catalyze the dehydration of cellulosic thermal insulating materials at a lower temperature and facilitate the generation of furfural and levoglucosenone, thus promoting the formation of char. These results provide useful information to understand the pyrolysis and fire retardancy mechanism of fire-retarded cellulose thermal insulation. Keywords Thermal degradation Á Thermal kinetics Á Fire retardant Á Cellulose fiber Á Thermal insulating APP Ammonium polyphosphate ATH Aluminum hydroxide E a Apparent activation energy (kJ mol-1) EGIM Expandable graphite fire-retardant insulating material FWO Flynn-Wall-Ozawa KAS Kissinger-Akahira-Sunose Py-GC/ MS Pyrolysis-gas chromatography-mass spectroscopy R Gas constant (8.314 J K-1 mol-1) SYIM Synergetic fire retardant insulating material T Absolute temperature (K) TG Thermogravimetry

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