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This study aims to determine the appropriate irradiation dose for induction of somaclonal variation in mass of unorganized parenchyma cells derived from sainfoin (Onobrychis viciifolia) tissues.

To investigate the feasibility of UV-B irradiation (312 nm), seeds and callus of sainfoin were exposed to five different intensities (20-100 per cent) for evaluating the effectiveness of phytochemical constituents and cellular behaviour.

Although percentage of seed viability reduced in 20 per cent intensity of UV-B irradiation compared with control seeds, the germination speed significantly enhanced from 3.58 to 5.42. The spectrophotometer analysis confirmed that concentrations of chlorophyll (a and b) decreased after UV-B exposure as compared with control callus. Also, carotenoid content showed significant differences among treated calli. Flavonoid and phenolic contents were observed to gradually increase when the non-irradiated callus subjected to 40 and 60 per cent intensities of UV-B irradiation, respectively. Observation on cellular behaviour such as determination of nuclear and cell areas, mitotic index and chromosomal aberrations were also detected to change in different intensities of UV-B irradiation. Fragmented and aneuploidy aberrations were only observed in exposed cells with more than 40 per cent intensity of UV-B irradiation.

In reality, radiocytological evaluation was proven to be essential in deducing the effectiveness of UV-B irradiation to induce somaclonal variation in callus tissue of sainfoin.

The purpose of this paper is to evaluate the potential of natural colourants from fruits of Ixora siamensis for coating applications, to study its glossiness and effectiveness against UV‐B irradiation.

In this study, natural colourants from the fruits of Ixora siamensis were extracted using trifluoroacetic acid‐methanol solution. Anthocyanins and organic acid variants were mixed together to form co‐pigments. Different concentrations of ferulic and gallic acid co‐pigments were added to a blended solution of poly (vinyl alcohol), PVA and anthocyanin (from Ixora siamensis) to form a coating system. The coatings were exposed to UV‐B irradiation at room temperature in air using a UV‐lamp which emitted radiation at 312 nm. The effects of UV‐B irradiation on the coating system were evaluated using glossiness test and UV‐visible spectroscopy.

Anthocyanins are unstable and can quickly lose their colour. One of the methods of preserving the stability of these pigments is by co‐pigmentation. Co‐pigmentation of anthocyanin with organic acid variants resulted in an increase in both hyperchromic effects (ΔA) and bathochromic shifts (Δλ). In this study, ferulic acids yielded better results compared to gallic acids.

Samples with co‐pigmentation give better result compared to the untreated samples. The addition of 0.5 and 1.0 per cent ferulic acid improves the gloss properties and resistivity of the samples towards the UV irradiation. Thus, in order to study the effectiveness of ferulic acid as additive and improving the properties of the samples, the percentage of ferulic acid added and exposure time could be increased.

The method developed provided a simple and efficient solution for improving the UV resistance of anthocyanin blend with poly (vinyl alcohol), PVA UV absorber. Effect of ferulic acid as UV absorber, if added in more concentration, can be further studied for optimization.

The social implication is the use of local plant species as a low cost source of natural pigments in coating system.

The method for improving the resistance towards UV irradiation of anthocyanin blend with poly (vinyl alcohol), PVA was novel and could find numerous applications for natural product based on plant pigment.

The purpose of this study is to synthesize a semiconductor photocatalyst which responds to both UV light and visible light in removal of organic dyes.

ZnO nanoparticles were pre-synthesised via sol-gel method using zinc nitrate tetrahydrate and methanamine at 90°C for 20 h. Subsequently, the as-synthesised ZnO nanoparticles were filtered, washed and dried. To synthesize ZnO-MnO₂ core shell nanocomposites (CSNs), 2:3 M ratio of KMnO₄ and MnSO₄ solution was stirred for an hour. Next, ZnO nanoparticles were added into the solution. The solution was heated at 160°C for 3 h for the formation of ZnO-MnO₂ CSNs. The structural, optical and photocatalytic properties of ZnO-MnO₂ CSNs were characterised by field emission scanning electron microscope, transmission electron microscopy (TEM), X-ray diffractometer and PL spectroscopy, respectively.

The photodegradation efficiencies of rhodamine B (RhB) dye by ZnO-MnO₂ CSNs as photocatalysts are 87.1 per cent under UV irradiation and 76.6 per cent under visible light irradiation, respectively. Their corresponding rate constants are 0.016 min⁻¹ under UV irradiation and 0.013 min⁻¹ under visible light irradiation. It can be concluded that N-deethylation was the dominant step during the photodegradation of RhB dye as compared to cycloreversion. The ZnO-MnO₂ CSNs demonstrated good photostability after three consecutive runs.

ZnO-MnO₂ CSN photocatalyst which could response to UV and visible light in degradation of RhB dye was synthesised using sol-gel method. The analysis shows that N-deethylation was the key photodegradation mechanism of RhB by ZnO-MnO₂ CSN.

The purpose of this paper is to use alternative polymerisation methods, i.e. UV irradiation to synthesise poly(acrylamide)/montmorillonite nanocomposite and characterise the composite.

Polymer/montmorillonite nanocomposite was synthesised by the polymerisation, induced by UV radiation and the structure of the composite was studied by means of FTIR, NMR(¹³ C, ²⁷Al and ²⁹Si) and X‐ray diffraction.

The poly(acrylamide)/montmorillonite nanocomposite was synthesised by UV irradiation, and its structures showed that the acrylamide was intercalated in the lamina of montmorillonite in bimolecular layers. FTIR and NMR analyses showed that there was no major chemical change of the polymer chain associated with the intercalation. The interaction between montmorillonite and polymer was mainly related with the van der Waals forces and hydrogen bonding, not with the bonding involved with the carbon atoms.

There are few reports on the synthesis and characterisation of polymer/montmorillonite composite prepared with UV radiation.

The alternative synthesis method using UV irradiation can provide a new way for the preparation of montmorillonite/acrylamide nanocomposite for the application in moisture and organic solvent vapour sensors, etc.

This provides a way for the synthesis of polymer/montmorillonite nanocomposite using polymerisation induced by UV radiation, which can be used in the thin membrane preparation for sensor and special application. Characterisation of the material revealed the structure of the nanocomposite, which would be helpful for the study of structure design and property improvement.

This paper aims to a newly designed photoresponsive four-armed graft copolymer was synthesised and characterised. The synthesised polymer contains photochemical group and a greater part of the cross-linkable functional group which is not affected by short wavelength when subject to under ultraviolet (UV) irradiation in film status.

The four-armed macroinitiator was prepared by reacting diethanol amine with poly [methyl-2-chloro-4-{7-(chloroacetyl) oxy]-2-oxo-2H-chromen-4-yl}-2-methylbutanoate] and acylating the product with chloroacetyl chloride. A grafting reaction with n-butyl methacrylate was carried out in the presence of the four-armed macroinitiator and the catalyst CuBr/2, 2′-bipyridyne at 90°C. All of the synthesised polymers were structurally characterised by Fourier transform infrared spectroscopy (FT-IR) and Hydrogen-1 Nuclear Magnetic Resonance (1H-NMR) spectra. Gel permeation chromatography was used to obtain the molecular weights of polymer.

1H-NMR, FT-IR and ultraviolet-visible (UV-Vis) spectroscopy demonstrated that the four-armed macroinitiator and the graft copolymer was successfully synthesised. The end-functionalised poly(methyl methacrylate) with 7-hydroxyl-4-chloromethyl coumarin was irradiated at the wavelength larger than 300 nm to create the cyclobutane ring in between the 7-hydroxyl-4-chloro methyl coumarin unities. To characterise the polymer and show the transformation of coumarin unities into photodimers, 1H-NMR, FT-IR and UV-Vis spectroscopy were used.

Graft copolymer containing coumarin has involves photocrosslinkable functional group, in which reactive functional group has attracted great interest from both industrial and academic fields. Their synthesis provides the opportunity for a compatible modification of the graft copolymer structure to develop adapted macromolecules for a range of end practices.

A photoresponsive graft copolymer can have a role in an active area of polymer chemistry research due to its uses in the areas of photolithography, liquid crystal, non-linear optical materials, laser dyes, fluorescence materials and future microelectronics.

Graft copolymers containing a photocrosslinkable functional group, and a star polymer may be prepared using the method described in this paper and then used in technological applications. The method discussed here also allows photoinduced reversible self-healing in solid polymers.

The purpose of this research is to synthesize Al₂O₃-ZnO thick films, study the effect of doping and optical excitation on their sensing properties and introduce an attractive candidate for acetone detection in practice.

ZnO nanoparticles doped with Al₂O₃ were prepared by sol-gel method and characterized via X-ray diffraction and field-emission scanning electron microscopy. The sensing properties to acetone were investigated with an irradiation of UV. The sensing mechanism was also discussed with UV-Vis spectroscopy.

The doping of Al₂O₃ promoted the sensing response and stability of ZnO nanoparticles. The optimum performance was obtained by 4.96 Wt.% Al₂O₃-ZnO. The response to acetone (1,000 ppm) was significantly increased to 241.81, even just at an operating temperature of 64°C. It was also demonstrated that optical excitation with UV irradiation greatly enhanced the sensing response and the sensitivity can reach up to 305.14.

The sensor fabricated from 4.96 Wt.% Al₂O₃-ZnO exhibited excellent acetone-sensing characteristics. It is promising to be applied in low power and miniature acetone gas sensors.

In the present research, the optimum performance was obtained by 4.96 Wt.% Al₂O₃-ZnO at a low operating temperature of 64°C. The sensing properties were enhanced significantly with optical excitation, and the sensing mechanism was discussed with UV-Vis spectroscopy which has been reported rarely before.

To discover new photochromic molecules suitable for various applications.

The synthesis of the new photochromic Aniline derivatives was accomplished by reaction of tetracyanoquinodimethane and anilines in polar solvents such as dimethylformamide.

A novel photochromic system had been designed and developed. The synthesis and photochromic properties of three aniline derivatives upon irradiation with ultraviolet light were studies in different solvents. The photochromic and thermochromic properties were affected markedly upon changing the solvent polarity. The new materials gave colourless to deep yellow coloration upon irradiation with ultraviolet, rendering them suitable candidates for optical storage media using the region of 700 nm.

A new photochromic system had been developed via a simple method. The new compounds showed photochromic, thermochromic, and solvatochromic properties making them potential candidates for many applications such as photo sensors, optical data storage, thermochromic sensors and heat sensitive materials.

The photochromic system was novel and hence the photochromic molecules were novel.

The purpose of this paper is to fall light on the possibility of using the biopolymer chitosan in gamma dose monitoring.

The chitosan films were irradiated to gamma rays in the range starting from 10 to 120 kGy at a dose rate of 1.4 kGy/h using ⁶⁰Co gamma source. The ultra violet and visible (UV/Vis) spectrophotometry were used to examine the optical properties of chitosan film. Also, Fourier transform infrared (FTIR) analysis was used to detect and trace any change in structural bands that may take place upon irradiation.

Increase in optical density of the chitosan film was recorded at 298 nm that correlated with increasing in the absorbed doses. Change in color of the film from pale yellow to denser yellow was detected upon increasing the absorbed doses. The close investigation for UV/Vis and FTIR analysis nominates the chitosan film to be used as a label-dosimeter in the range of 10–120 kGy depending on chitosan concentrations. The chitosan film has an excellent stability in different environmental conditions with ±3.7% uncertainty in measurements (2σ, approximately equal to a 95% confidence level).

Chitosan film may be used as a medium and high-dose monitor with an acceptable overall uncertainty in routine radiation processing

The useful dose range from 10 to 80 kGy was detected for different concentrations of chitosan (0.5, 1, 1.5 Wt%) that correlated with increasing the absorbed dose, which is assigned to the linear parts in the target response curves. For the dose range 10–120 kGy, the film may be used as label dosimeter with detected color change from pale yellow to dense yellow.

In the present work, under severe conditions of an inert atmosphere and high temperature, epoxidized natural rubber (ENR) with 25 per cent epoxidation level reacts with different aliphatic amine compounds such as ethyl amine (EA), propyl amine (PA) and butyl amine (BA) to prepare ENR/EA, ENR/PA, ENR/BA compounds as, respectively. The produced compounds were characterized by Fourier transform infrared spectroscopy and oxirane oxygen content determination. Different concentrations of the produced compounds were added to epoxy and urethane acrylate coating formulations to evaluate them as corrosion inhibitors for mild steel under UV irradiation. Corrosion resistance tests and weight loss measurements of the coated steel panels were made. It was found that coating formulations containing the prepared ENR/EA compound could protect metal surface from corrosion, and corrosion inhibitors efficiency of the prepared compounds were arranged as follows: ENR/EA > ENR/PA > ENR/BA. The optimum concentrations for all inhibitors which give the best inhibition efficiency for corrosion are 0.4-0.6 phr.

Corrosion scratch tests were carried out according to ASTM D 1,654-92 (2000). The weight loss of coated steel was measured according to ASTM D 2,688-94 (1999). The measurement of film hardness was carried out with a Wolff–Wilborn pencil hardness tester according to ASTM D 3,363 (2000).

It was found that coating formulations containing the prepared ENR/EA compound could protect metal surface from corrosion and corrosion inhibitors efficiency of the prepared compounds were arranged as follows: ENR/EA > ENR/PA > ENR/BA. The optimum concentrations for all inhibitors are 0.4-0.6 g/100g coating.

A highly efficient and economically corrosion inhibitors for mild steel were prepared from ENR and series of aliphatic amines.

To evaluate the photochromic performance of photochromic compounds in polymer matrices.

The epoxy resin doped with photochromic fulgide were prepared and the effect of UV irradiation were studied using spectrophotometer. The reversible reaction was effected using white light. The effect of heat was also determined.

A film of fulgide 1‐E doped in epoxy polymer was irradiated with UV light (366 nm), the film turned pink. The later colour was switched back to the original colour when the film was irradiated with a white light. The photocoloration and photobleaching obeyed first order rate equations with rate constants being 4.19×10⁻³ s⁻¹ and 2.86×10⁻² s⁻¹, respectively. It was found that the film showed a good fatigue resistance. Another film was preheated at 80°C for 1‐4 h. No change in the UV absorption spectra of the film was observed. Similarly, the photocoloration and photobleaching of the annealed film showed first order rate equations with rate constants being 8.77×10⁻³ s⁻¹ and 4.02×10⁻²s⁻¹, respectively. Interestingly, the photocoloration and photobleaching reactions of the annealed film were faster than those of the non‐annealed film.

The epoxy resin doped photochromic fulgides described in the present paper was prepared and studied. The principle of study established can be applied to any type of resin or to any type of photochromic compounds.

The photochromic materials developed can be used for different applications, such as coatings and holography.

The method developed may be used to enhance the performance of photochromic materials.