Combined effect of hindered amine light stabilizer and ultraviolet absorbers on photodegradation of poly(vinyl chloride)

The combined effect of a basic hindered amine light stabilizer (HALS) and ultraviolet absorbers (UVAs) on casted poly(vinyl chloride) (PVC) films, during photodegradation, was studied by color change, ultraviolet‐visible (UV–vis) spectroscopy, Fourier‐transform infrared (FTIR) spectroscopy, and viscosity‐average molecular weight. It was found that the basic amine groups in the HALS (T770) could promote the dehydrochlorination, thereby accelerating the photooxidation of PVC films. Meanwhile, T770 could scavenge the radicals formed and restrain the aging of PVC to some extent. The above‐mentioned aspects were competing factors: the former played a dominant role during the first 100 h, while the latter counteracted the former effect to some extent between 100 and 300 h. A benzotriazole derivative (UV326) absorbs more UV radiation in the UV‐A region (320–400 nm), which mainly causes the photodegradation of PVC samples, than a benzophenone derivative (UV531). Thus, UV326 is a more efficient UV absorber than UV531 in prohibiting the photooxidation and chain scission of PVC films. The combination of T770 and UV326 effectively protected PVC films from dehydrochlorination and photooxidation. The combination of T770 and UV531 accelerated the dehydrochlorination and discoloration of PVC films. J. VINYL ADDIT. TECHNOL., 2012. © 2012 Society of Plastics Engineers     

Preparation and characterization of PS‐PMMA/ZnO nanocomposite films with novel properties of high transparency and UV‐shielding capacity

High transparent and UV‐shielding poly (styrene)‐co‐poly(methyl methacrylate) (PS‐PMMA)/zinc oxide (ZnO) optical nanocomposite films were prepared by solution mixing using methyl ethyl ketone (MEK) as a cosolvent. The films were characterized by X‐ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible (UV–vis) spectra, high‐resolution transmission electron microscopy (HR‐TEM), and atomic force microscope (AFM). Cross‐section HR‐TEM and AFM images showed that the ZnO nanoparticles were uniformly dispersed in the polymer matrix at the nanoscale level. The XRD and FTIR studies indicate that there is no chemical bond or interaction between PS‐PMMA and ZnO nanoparticles in the nanocomposite films. The UV–vis spectra in the wavelength range of 200–800 nm showed that nanocomposite films with ZnO particle contents from 1 to 20 wt % had strong absorption in UV spectrum region and the same transparency as pure PMMA‐PS film in the visible region. The optical properties of polymer are greatly improved by the incorporation of ZnO nanoparticles. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Fabrication and characterization of graphene oxide modified polycarboxylic by in situ polymerization

Graphene oxide (GO) was modified by in situ esterification reaction with isopentenol polyoxyethylene ether (IPEG) to obtain GO precursor (GO-IPEG) with some polymerization activity. GO-modified polycarboxylic (GO-PCE) was prepared by GO-IPEG and acrylic acid (AA) using the method of in situ polymerization. The molecular structure of GO-IPEG and GO-PCE was characterized by Fourier transform infrared spectroscopy (FTIR), Raman spectra, and nuclear magnetic resonance (NMR). The dispersion properties and dispersion stability of GO-IPEG and GO-PCE in water solution were studied by ultraviolet–visible (UV–vis) absorption spectra, zeta potential, and atomic force microscope. The results of FTIR, Raman, ¹H-NMR, and ¹³C-NMR indicate that IPEG was successfully grafted onto the surface of GO and then fabricated with AA by in situ free-radical polymerization. The results of UV–vis and zeta potential show that GO nanosheets have a better dispersion in GO-IPEG or GO-PCE system when the reaction time of GO and IPEG is 1 h, and the dispersion stability can reach up to 1 month. The better dispersion and application property are confirmed by atomic force microscopy image and cement fluidity, water reducing rate, and compression strength. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 48316.     

Preparation and Characterization of Conductive Polyaniline/Silver Nanocomposite Films and Their Antimicrobial Studies

Silver (Ag) nanoparticles are known to hold an important place in nanotechnology, and studies herein present the preparation and characterization of Ag metallic nanoparticles bearing antibacterial properties. In situ polymerization was used to prepare the conductive polymer polyaniline (PANI) and polyaniline/silver (PANI/Ag) nanocomposites. Increases in electrical conductivities of the nanocomposite films were observed compared to neat PANI, whereby these increases may be a result of the Ag doping effect or its complex formation. Spectroscopic techniques, such as, UV–Vis, FTIR, and photoluminescence were used for the characterizations of PANI and PANI/Ag nanocomposites. UV–Vis and FTIR data showed the quinoid units along the polymer chain being affected, such that strong interactions between Ag nanoparticles and quinoidal sites of PANI were presumed. The PANI/Ag nanocomposites showed higher photoluminescence intensities than neat PANI. TGA analyzes were used to determine weight losses and thermostabilities of PANI and PANI/Ag nanocomposites. Scanning electron microscopy was used for morphological evaluations of the nanoparticles and films, where the micrographs revealed that Ag nanoparticles were well dispersed and isolated in nanocomposite films. The presence and distribution of the Ag nanoparticles in PANI film matrix were analyzed by EDX. Antimicrobial properties of the nanocomposite films obtained were also explored. POLYM. ENG. SCI., 59:E182–E194, 2019. © 2018 Society of Plastics Engineers     

Physical properties of epoxy resin/titanium dioxide nanocomposites

A polymeric nanocomposite system (nanodielectric) was fabricated, and its mechanical properties were determined. The fabricated nanocomposite was composed of low concentrations of monodispersed titanium dioxide (TiO₂) nanoparticles and an epoxy resin specially designed for cryogenic applications. The monodispersed TiO₂ nanoparticles were synthesized in an aqueous solution of titanium chloride and polyethylene glycol and subsequently dispersed in a commercial‐grade epoxy resin (Araldite® 5808). Nanocomposite thin sheets were prepared at several weight fractions of TiO₂. The morphology of the composites, determined by transmission electron microscopy, showed that the nanoparticles aggregated to form particle clusters. The influence of thermal processing and the effect of filler dispersion on the structure–property relationships were identified by differential scanning calorimetry and dynamic mechanical analysis at a broad range of temperatures. The effect of the aggregates on the electrical insulation properties was determined by dielectric breakdown measurements. The optical properties of the nanocomposites and their potential use as filters in the ultraviolet–visible (UV–vis) range were determined by UV–vis spectroscopy. POLYM. ENG. SCI., 2011. © 2010 Society of Plastics Engineers     

Thermal stability of poly(vinyl chloride)/layered double hydroxide nanocomposites

Effects of nanoscale dispersed layered double hydroxides (LDHs) on thermal stability of poly(vinyl chloride) (PVC) in thermal and thermooxidative degradation processes are investigated by dynamic and isothermal thermogravimetric analysis (TGA), discoloration test, fourier transform infrared (FTIR), and ultraviolet‐visible (UV‐vis) spectroscopic techniques. During both stages of thermal degradation, the degradation temperatures, including onset degradation temperature and temperature of the maximum degradation rate, increase, and the final residue yield of the PVC/LDH nanocomposites reaches 14.7 wt %, more than double that for neat PVC. The thermooxidative degradation process is more complex. During the first two stages, the presence of nanoscale dispersed LDH particles enhances the thermal stability, whereas in the last stage accelerates the thermal degradation possibly due to the accumulation of heat released. Additionally, the studies of the isothermal thermooxidative degradation process by FTIR and UV‐vis spectra indicate that both polyene backbone formation and some carbonyl groups are simultaneously developed. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Structural and thermal characterization of poly(2‐chloroaniline)/red mud nanocomposite materials

We report the synthesis and characterization of a series of conducting poly(2‐chloroaniline) (P2ClAn)/red mud (RM) nanocomposite materials. The polymerization of 2‐chloroaniline in an aqueous medium in the presence of (NH₄)₂S₂O₈ and RM resulted in the formation of a nanocomposite (P2ClAn/RM). The extent of P2ClAn loading in the composites increased with increasing oxidant and monomer concentrations but decreased with RM. The properties of the nanocomposites were characterized with Fourier transform infrared (FTIR), ultraviolet–visible (UV–vis), conductivity measurements, scanning electron microscopy, thermogravimetric analysis, and differential scanning calorimetry analysis. The inclusion of P2ClAn in the composites was confirmed by FTIR studies. The UV–vis spectra of P2ClAn/RM nanocomposites were similar to that of P2ClAn. The conductivity changed in all the composites prepared under various conditions. Thermogravimetric analyses revealed the enhanced thermal stabilities of the nanocomposites with respect to P2ClAn. Morphological images of the as‐synthesized materials were also investigated with scanning electron microscopy and environmental scanning electron microscopy. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006     

Synthesis,characterization, and properties of new conducting polyaniline/copper sulfide nanocomposites

This article reports the facile synthesis of copper sulfide (CuS)/polyaniline (PANI) nanocomposites by in situ polymerization. The composites were characterized by scanning electron microscopy (SEM), UV–visible and Fourier transform infrared (FTIR) spectroscopy, X‐ray diffraction (XRD), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). SEM analysis showed that the metal sulfide nanoparticles were uniformly dispersed in the polymer matrix. The characteristic peaks in FTIR and UV–vis spectra of PANI were found to be shifted to higher wave numbers in PANI/CuS composite, which is attributed to the interaction of CuS nanoparticles with PANI chain. XRD pattern revealed the structurally ordered arrangement of polymer composite and this regularity increases with increase in concentration of nanoparticles. Glass transition temperature of the nanocomposite increased with increase in the concentration of nanoparticles and it indicated the ordered arrangement of the polymer composite than PANI. TGA studies indicated excellent thermal stability of polymer nanocomposite. The electrical properties of nanocomposites were studied from direct current and alternating current resistivity measurement. Conductivity, dielectric constant, and dissipation factor of the nanocomposite were significantly increased with the increase in CuS content in the nanocomposite. The enhancement of these properties suggests that the proposed PANI/CuS nanocomposites can be used as multifunctional materials for nanoelectronic devices. POLYM. ENG. SCI., 54:438–445, 2014. © 2013 Society of Plastics Engineers     

Preparation and characterization of silica sol/fluoroacrylate core–shell nanocomposite emulsion

The silica sol/fluoroacrylate core?Cshell nanocomposite emulsion was successfully synthesized via traditional emulsion polymerization through grafting of KH-570 onto silica particles. Comparing the performance of the polyacrylate copolymer, the fluorinated polyacrylate copolymer and the silica sol/fluoroacrylate core?Cshell nanocomposite emulsion, we can come to a conclusion that the silica sol/fluoroacrylate core?Cshell nanocomposite emulsion presents significantly excellent performance in all aspects. The products were characterized by Fourier transform infrared (FTIR), photon correlation spectroscopy (PCS), transmission electron microscopy (TEM), thermogravimetry (TGA), Contact angle and UV?Cvis analyses techniques. The chemical structure of polyacrylate copolymer, fluorinated polyacrylate copolymer and silica sol/fluoroacrylate nanocomposite were detected by FTIR. The size and stability of emulsion latex particles were determined by PCS technique. TEM analysis confirmed that the resultant latex particle has the core?Cshell structure, obviously. The water absorption and contact angle data also showed that the silica sol/fluoroacrylate nanocomposite film has good hydrophobic performance. TGA analysis indicated the weight loss of the silica sol/fluoroacrylate nanocomposite film begins at around 350?°C which testifies its good thermal stability. The UV?Cvis spectroscopy analysis showed that the silica sol/fluoroacrylate nanocomposite film possess UV?Cvis shielding effect when the added volume amount of KH570 modified silica sol is up to 5?mL. Therefore, the excellent properties of hydrophobicity, thermodynamics and resistance to ultraviolet provide the silica sol/fluoroacrylate nanocomposite film with potential applications in variety fields. In addition, the formation mechanism of core?Cshell structure silica sol/fluoroacrylate nanocomposite latex particles was speculated.     

Synthesis and characterization of rutile titanium dioxide/polyacrylate nanocomposites for applications in ultraviolet light‐shielding materials

Rutile titanium dioxide (TiO₂)/poly(methyl methacrylate‐acrylic acid‐butyl acrylate) nanocomposites were synthesized via seeded emulsion polymerization and characterized by Fourier transmission infrared, dynamic light scattering, X‐ray diffraction, ultraviolet–visible (UV–vis) spectroscopy, scanning electron microscopy, transmission electron microscopy, and thermogravimetric analysis to study their UV‐shielding property. The effects of the nanoseed types, surfactant concentrations, and functional monomer amounts on the polymerization conversion, particle size, emulsion stability, and morphologies of the resulting nanocomposites were investigated. The dependence of UV‐shielding performance on the nanoparticle content and dispersion was also explored. The optimized results are obtained with 2 wt% of TiO₂ nanoparticles addition, and the effectiveness of UV shielding is significantly increased by using the synthesized rutile nano‐TiO₂/polyacrylates, for which the nanocomposite coating with a thickness of 200 μm could block up to 99.99% of UV light (≤350 nm) as confirmed by UV–vis spectrometry. POLYM. COMPOS., 36:8–16, 2015. © 2014 Society of Plastics Engineers     

Dodecylbenzenesulfonic acid micelles assisted in situ preparation and enhanced thermoelectric performance of semiconducting polyaniline–zirconium oxide nanocomposites

Herein, we report in situ preparation of dodecylbenzenesulfonic acid (DBSA) micelles assisted polyaniline (Pani)/zirconium oxide (ZrO₂) nanocomposites (Pani/ZrO₂) by using K₂S₂O₈ as an oxidizing agent. Thus prepared nanocomposites were characterized by SEM, FTIR, XRD and UV–vis spectrophotometry. DBSA acted as dopant/surfactant, and the incorporation of ZrO₂ nanoparticles improved the stability, electrical and thermal properties of nanocomposites. From the results of UV–vis absorbance it was observed that Pani/ZrO₂ nanocomposite was more stabilized under UV light than Pani. DC electrical conductivity retention was studied by isothermal and cyclic ageing techniques and was observed to be better than Pani under ambient environmental conditions.     

Effects of preparation method on microstructure and properties of UV‐curable nanocomposite coatings containing silica

UV‐curable nanocomposites were prepared by the blending method or the in situ method with nanosilica obtained from a sol–gel process. The microstructure and properties of the nanocomposite coatings were investigated using ²⁹Si‐NMR cross‐polarization/magic‐angle spinning, transmission electron microscopy (TEM), Fourier transform IR (FTIR), differential scanning calorimetry (DSC), and UV–visible (UV–vis) spectra, respectively. The NMR and TEM showed that during the blending method, tetraethyl orthosilicate (TEOS) completely hydrolyzed to form nanosilica particles, which were evenly dispersed in the polymer matrix. However, for the in situ method, TEOS partially hydrolyzed to form some kind of microstructure and morphology of inorganic phases intertwisted with organic molecules. FTIR analysis indicated that the nanocomposites prepared from the in situ method had much higher curing rates than those from the blending method. DSC and UV–vis measurements showed that the blending method caused higher glass‐transition temperatures and UV absorbance than the in situ method. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 1119–1124, 2005     

UV-protection,tribology, and mechanical properties of ZnO-containing polyamide composites

Most polymer-based materials do not exhibit ultraviolet (UV) protection or wear resistance properties, thereby leading to poor packaging functions. This study provides an approach that simultaneously improves the UV protection and tribological functions of melt-processed polyamide (PA)-based composites by the addition of in-house produced hexagonal-shaped nano-zinc oxide (ZnO) particles. The 5 wt % ZnO-filled PA composite exhibited significant photodegradation protection (84%) with a well-balanced friction coefficient and wear resistance properties. The 1 wt % ZnO-filled PA composite also exhibited significant photodegradation protection (84%) but with a lower friction coefficient and strong wear resistance, while the 7 wt % ZnO-filled PA composite displayed strong photodegradation protection (94%) with poor wear resistance. The results suggest that owing to their UV stability and wear resistance, the low ZnO-filled PA composites show great potential as plastic materials in different applications such as active packaging. In addition, all the ZnO-filled PA composites exhibited improved mechanical properties relative to those of the neat PA. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48418.     

Spectroscopic study of the modification of cellulose with polyethylenimines

The reaction of cellulose with polyethylenimines (PEIs) was studied using diffuse reflectance ultraviolet–visible (UV–vis) spectroscopy, diffuse reflectance FTIR spectroscopy, and standard colorimetry. PEIs were applied from aqueous solutions at the natural pH (pH ～ 11) and at pH = 6. The obtained materials were exposed to different thermal treatments in air. Celluloses treated at pH = 11 suffer the reversible formation of amine bicarbonate salts. This reaction was not observed in celluloses treated at pH = 6 because of the protonation of the amine groups. In all treated celluloses, the PEI amine groups reacted with cellulose carbonyl groups at moderate temperatures to form Schiff bases, which were responsible for the yellowing of the material. At higher temperatures other oxidation products were detected in the UV–vis and infrared spectra. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 2196–2202, 2004     

Flexible oligomeric silicon-containing poly(ether-azomethine)s obtained from epoxide derivatives. Synthesis and characterization

Three new diamines derived from epoxide compounds were synthesized. The preparation of diamine monomers implied the reaction between a phenoxyalkyloxirane (alkyl: H, methyl, isopropyl) and bisphenol A, obtaining the respective aliphatic diols, which produced the corresponding dinitro derivatives. Finally, these derivatives were reduced by using palladium/carbon activated as catalyst and hydrazine as a hydrogen source. Then, six oligomeric poly(ether-azomethine)s (PEAzMs) were obtained from a polycondensation reaction between the new diamines and bis(4-formylbiphenyl-4-yl)dialkylsilane (alkyl: methyl, phenyl) with 84–93% yields. The structural characterization of the diamines and PEAzMs was performed by elemental analysis, infrared spectroscopy, and nuclear magnetic resonance spectroscopy (¹H, ¹³C, and ²⁹Si). Furthermore, polymers were analyzed by solubility tests, gel permeation chromatography, ultraviolet–visible (UV–vis) spectroscopy, thermogravimetry, and differential scanning calorimetry analysis. The results showed PEAzMs with 2–11 repetitive units, where the design of the monomers allowed to obtain improved solution processability in comparison with previously reported silylated poly(azomethine)s and good thermal stability. Additionally, all samples showed high transparency in the UV–vis region. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 48055.     

Synthesis,characterization, and ionic conductivity of electrospun organic–inorganic hybrid gel electrolytes

In this work, we described the synthesis of organic–inorganic hybrid gel electrolytes combining electrospinning, sol–gel, and ultraviolet (UV) curing techniques in order to investigate their ionic conductivity properties. First, 3-glycidyloxypropyl trimethoxysilane modified polyamic acid and alkoxysilane functional poly(dimethyl siloxane) were electrospun together. Then, the following thermal imidization, the obtained fiber was cured in the UV curable gel formulation. To improve the interaction between fiber and gel matrix, 3-(trimethoxysilyl)propyl methacrylate was partly hydrolyzed and then used as a bifunctional crosslinker. Finally, the membrane was soaked into 0.5 M LiFP₆ salt solution to obtain organic–inorganic hybrid gel electrolytes. The chemical structure, ionic conductivity, and range of electrochemical stability window of the photocured nanocomposite electrolytes were investigated by using FTIR, thermogravimetric analysis, differential scanning calorimetry, electrochemical impedance spectroscopy, linear sweep voltammetry, and SEM analysis. The acquired results from experiments indicate that a convenient nanocomposite electrolyte for lithium-ion batteries with high electrolyte (Li salt) uptake, adequate conductivity (1.02 × 10⁻³ S cm⁻¹) at ambient temperature and electrochemically stable between 1 and 6 V had been prepared. POLYM. ENG. SCI., 60:619–629, 2020. © 2019 Society of Plastics Engineers     

NIR-responsive Fe3O4@PPy nanocomposite for efficient potential use in photothermal therapy

In this work, superparamagnetic Fe₃O₄@PPy nanocomposite with core-shell structure having strong near-infrared (NIR) absorption is synthesized via a facile two-step modified procedure. The prepared nanocomposite samples are characterized by UV–vis, FTIR, SEM, TEM, VSM, and XRD. The effects of laser power density (1.5–2.5 W cm⁻²) and aqueous concentration (0.01–0.2 mg ml⁻¹) of the nanocomposite on the photothermal performance are investigated in the NIR region (808 nm). At 0.1 mg ml⁻¹ concentration, the temperature reaches up to 50.1°C, 64.1°C, and 78.4°C within 10 min, under 1.5 W cm⁻², 2.0 W cm⁻², and 2.5 W cm⁻² NIR laser power density values, respectively. Photothermal conservation efficiency is calculated as 43.9% and the nanocomposite exhibits excellent photothermal stability. In summary, the core-shell Fe₃O₄@PPy nanocomposite is a promising candidate for photothermal therapy and simultaneous magnetic field-guided treatments.     

PA6/类水滑石纳米复合材料的制备与性能研究

将自制的双甲氧基苯甲酸根离子插层的类水滑石(MgAl-PMOBA-LDHs)分散到己内酰胺（CL）水溶液中,利用CL原位水解开环聚合制备了聚酰胺6（PA6）/MgAl-PMOBA-LDHs纳米复合材料,并通过透射电子显微镜、X射线衍射仪、紫外吸收光谱仪、热分析等对其性能进行了表征。结果表明,MgAl-PMOBA-LDHs 在复合材料中呈纳米级均匀分散,少量均匀分散的MgAl-PMOBA-LDHs 使复合材料对波长为320~380 nm的紫外线吸收效果明显;少量均匀分散的MgAl-PMOBA-LDHs 起到了很好的异相成核剂的作用,不仅提高了PA6的结晶温度,而且也提高了其结晶度;部分板层剥离的MgAl-PMOBA-LDHs 明显有助于PA6 的γ 晶型的产生。     

Impact of vanadium-, sulfur-, and dysprosium-doped zinc oxide nanoparticles on various properties of PVDF/functionalized-PMMA blend nanocomposites: Structural,optical, and morphological studies

The polymeric blend was fabricated with crystalline poly(vinylidene fluoride) (PVDF)/amorphous functionalized-poly(methyl methacrylate) (PMMA) in 70/30 w/w ratio by chemical mixing method. Functionalization of PMMA was achieved with 2-amino-5-nitrobenzoic acid. The prepared polymer blend was used as a matrix to synthesize nanocomposites with undoped/doped zinc oxide (ZnO) nanoparticles. Doping in ZnO was achieved with vanadium, sulfur, and dysprosium elements as a dopant. The structural, optical, electronic, and morphological properties of undoped/doped nanosized ZnO and blended nanocomposites were accessed through sophisticated analytical techniques, that is, Fourier transform infrared (FTIR), ultraviolet–visible (UV–vis), UV–vis–diffuse reflectance spectra, nuclear magnetic resonance, fluorescence spectroscopy, X-ray diffraction (XRD), transmission electron microscopy, and scanning electron microscopy. The FTIR band at 1165–1176 cm⁻¹ in functionalized-PMMA indicate the formation of aliphatic C-N bond along with aromatic ¹H chemical shift (δ) at 7.134, 7.829 and 8.210 ppm confirm the successfully functionalization of PMMA. The prominent XRD peak at 2θ = 20.8° in nanocomposites shown improvement in β-phase of PVDF. The results show that Dy doped ZnO nanoparticles create remarkable effect on various properties of nanocomposites. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47116.     

Synthesis of luminescent polymers in the UV light region from dimethacrylate monomer using novel quinoline dyes

This study aims at thermal and morphological features, as well as the degree of conversion these luminescent polymers obtained using a dimethacrylate monomer, and quinoline dyes as photoinitiator. The photoinitiators provide a fluorescent propriety to the final polymer. Thermal properties such as thermal stability, steps of mass loss, and glass transition are obtained by thermogravimetry-differential thermal analysis and derivative thermogravimetric and differential scanning calorimetry. Using the mid-infrared spectroscopy, it is possible to calculate the degree of conversion/rate of polymerization; the data indicate that the quinoline derivatives could be used as photoinitiators in lower concentration (0.1%) resulting in solid rigid polymers with higher conversion (74.24, 71.81, 66.36, and 61.09%). The morphological characteristics of polymers are analyzed by scanning electronic microscopy. Finally, solid ultraviolet–visible (UV–vis) analysis shows a bathochromic shift, due to the stabilization of the molecules in the solid state, compared to liquid UV–vis analysis. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47461.