Acrylic Content Research Articles

Tailorable acrylate-endcapped urethane-based polymers for precision in digital light processing: Versatile solutions for biomedical applications

Bioengineering seeks to replicate biological tissues exploiting scaffolds often based on polymeric biomaterials. Digital light processing (DLP) has emerged as a potent technique to fabricate tissue engineering (TE) scaffolds. However, the scarcity of suitable biomaterials with desired physico-chemical properties along with processing capabilities limits DLP's potential. Herein, we introduce acrylate-endcapped urethane-based polymers (AUPs) for precise physico-chemical tuning while ensuring optimal computer-aided design/computer-aided manufacturing (CAD/CAM) mimicry. Varying the polymer backbone (i.e. poly(ethylene glycol) (PEG) versus poly(propylene glycol) (PPG)) and photo-crosslinkable endcap (i.e. di-acrylate versus hexa-acrylate), we synthesized a series of photo-crosslinkable materials labeled as UPEG2, UPEG6, UPPG2 and UPPG6. Comprehensive material characterization including physico-chemical and biological evaluations, was followed by a DLP processing parametric study for each material. The impact of the number of acrylate groups per polymer (2 to 6) on the physico-chemical properties was pronounced, as reflected by a reduced swelling, lower water contact angles, accelerated crosslinking kinetics, and increased Young's moduli upon increasing the acrylate content. Furthermore, the different polymer backbones also exerted a substantial effect on the properties, including the absence of crystallinity, remarkably reduced swelling behaviors, a slight reduction in Young's modulus, and slower crosslinking kinetics for UPPG vs UPEG. The mechanical characteristics of DLP-printed samples showcased the ability to tailor the materials' stiffness (ranging from 0.4 to 5.3 MPa) by varying endcap chemistry and/or backbone. The in vitro cell assays confirmed biocompatibility of the material as such and the DLP-printed discs. Furthermore, the structural integrity of 3D scaffolds was preserved both in dry and swollen state. By adjusting the backbone chemistry or acrylate content, the post-swelling dimensions could be customized towards the targeted application. This study showcases the potential of these materials offering tailorable properties to serve many biomedical applications such as cartilage TE.

Phosphorus-Based Flame-Retardant Acrylonitrile Butadiene Styrene Copolymer with Enhanced Mechanical Properties by Combining Ultrahigh Molecular Weight Silicone Rubber and Ethylene Methyl Acrylate Copolymer.

The present work proposes to investigate the effect of an ultrahigh molecular weight silicone rubber (UHMW-SR) and two ethylene methyl acrylate copolymers (EMA) with different methyl acrylate (MA) content on the mechanical and fire performance of a fireproof acrylonitrile butadiene styrene copolymer (ABS) composite, with an optimum amount of ammonium polyphosphate (APP) and aluminum diethyl phosphinate (AlPi). ABS formulations with a global flame retardant weight content of 20 wt.% (ABS P) were melt-compounded, with and without EMA and UHMW-SR, in a Brabender mixer. During this batch process, ABS P formulations with UHMW-SR and/or EMA registered lower torque values than those of ABS P. By means of scanning electron microscopy (SEM), it was possible to observe that all ABS composites exhibited a homogenous structure without phase separation or particle agglomeration. Slightly improved interfacial interaction between the well-dispersed flame-retardant particles in the presence of EMA and/or UHMW-SR was also noticed. Furthermore, synergies in mechanical properties by adding both EMA and UHMW-SR into ABS P were ascertained. An enhancement of molecular mobility that contributed to the softening of ABS P was observed under dynamic mechanical thermal analysis (DMTA). An improvement of its flexibility, ductility and toughness were also registered under three-point-bending trials, and even more remarkable synergies were noticed in Charpy notched impact strength. Particularly, a 212% increase was achieved when 5 wt.% of EMA with 29 wt.% of MA and 2 wt.% of UHMW-SR in ABS P (ABS E29 S P) were added. Thermogravimetric analysis (TGA) showed that the presence of EMA copolymers in ABS P formulations did not interfere with its thermal decomposition, whereas UHMW-SR presence decreased its thermal stability at the beginning of the decomposition. Although the addition of EMA or UHMW-SR, as well as the combination of both in ABS P increased the pHRR in cone calorimetry, UL 94 V-0 classification was maintained for all flame-retarded ABS composites. In addition, through SEM analysis of cone calorimetry sample residue, a more cohesive surface char layer, with Si-O-C network formation confirmed by Fourier transform infrared (FTIR), was shown in ABS P formulations with UHMW-SR.

Acrylic acid -co- sodium acrylate copolymers synthetized in supercritical carbon dioxide: Is it possible to pre-neutralize polymers at high pressure?

This study focuses on the polymerization of acrylic acid together with sodium acrylate, commonly performed in traditional solvents, using supercritical carbon dioxide. This compressed polymerization solvent offers benefits like producing pure, dry polymers by a simple depressurization process. Thermally initiated free-radical polymerizations in supercritical CO2 were carried out, aiming to obtain a pre-neutralized polymer at the end of the reaction. The impact of sodium acrylate content on polymer physicochemical properties was analyzed. Conversions ranged from 86.9% to 96.7%, and sodium acrylate incorporation was verified using various analytical methods. The polymerizations displayed characteristic molar mass distributions, indicating continuous and dispersed phase polymerizations. Additionally, rheological measurements of polymer aqueous solutions revealed that viscosity increased with higher average molar mass and was responsive to pH and the presence of monovalent and divalent ions. This CO2-based approach presents a promising method for clean and safe polymer production.

Gelation of copolymers of acrylamide and sodium acrylate upon coordination with Cu2+ ions in concentrated solutions

The phase state of Cu2+ complexes with acrylamide and sodium acrylate copolymers at different copolymer concentrations and components molar ratios was studied. The change in complex stoichiometry from 2 to 3 carboxylate groups per Cu2+ ion was detected with an increase of copolymer concentration. In the concentrated solutions of copolymers, gelation is observed upon addition of Cu2+ ions, with the lowest concentration of copper required for gelation decreasing with the increase in copolymer concentration. These hydrogels are attributed to the formation of meta-stable inter-polymer metal complexes, which are able to persist due to a low segment mobility. The phase separation of complexes is shown to be associated with the bidentate coordination of carboxylate groups to Cu2+ ions, while the hydrogels formed in concentrated solutions mostly consist of bridging structures. Gelation threshold corresponds to the second critical concentration of poly(acrylamide-co-sodium acrylate) and is lower for copolymers with the higher molecular weight. Low acrylate content in the copolymers prevents collapse of the hydrogels caused by the salting-out effect. A higher gel content can be reached by increasing the copolymer concentration or the molar ratio of copper ions to carboxylate groups, with the latter reducing the swelling degree.

High-performance aluminum nitride made by Vat photopolymerization through optimization of resin refractive index and plasticizer content

In this study, we evaluated the effects of three resins with different refractive index on the viscosity and curing behavior of aluminum nitride (AlN) ceramic suspensions. Our findings indicate that the viscosity of the AlN suspensions increased with the concentration of polyethylene glycol o-phenylphenyl ether acrylate (OPPEA). Conversely, the viscosity decreased with increasing concentrations of cyclic trimethylolpropane formal acrylate (CTFA) and ethylene glycol phenyl ether acrylate (PHEA). Regarding the curing behavior, the AlN ceramic suspension prepared with OPPEA exhibited the largest cure depth and excess width, whereas the suspension prepared with CTFA had the lowest cure depth and excess width. Further analysis of the sensitivity and critical energy revealed that the suspension containing OPPEA demonstrated the highest sensitivity in the vertical direction and the lowest sensitivity in the horizontal direction. This implies that the smallest critical energy is in the vertical direction, and the largest critical energy is in the horizontal direction. Additionally, an increase in the content of the plasticizer dibutyl phthalate (DBP) was beneficial for reducing cracks in the AlN ceramic debinding bodies. Finally, high-performance AlN ceramics were produced, exhibiting a relative density exceeding 98 %, a bending strength of 470.39 ± 6.5 MPa, and a thermal conductivity of 163.45 W/m·K.

Cationic Hydrogels Modulate Neural Stem and Progenitor Cell Proliferation and Differentiation Behavior in Dependence of Cationic Moiety Concentration in 2D Cell Culture.

The central nervous system (CNS) has a limited regenerative capacity because a hostile environment prevents tissue regeneration after damage or injury. Neural stem/progenitor cells (NSPCs) are considered a potential resource for CNS repair, which raises the issue of adequate cultivation and expansion procedures. Cationic charge supports the survival and adhesion of NSPCs. Typically, tissue culture plates with cationic coatings, such as poly-l-ornithine (PLO), have been used to culture these cell types (NSPCs). Yet presently, little is known about the impact of cationic charge concentration on the viability, proliferation, and differentiation capacity of NSPCs. Therefore, we have recently developed well-defined, fully synthetic hydrogel systems G1 (gel 1) to G6 (gel 6) that allow for the precise control of the concentration of the cationic trimethylaminoethyl acrylate (TMAEA) molecule associated with the polymer in a range from 0.06 to 0.91 μmol/mg. When murine NSPCs were cultured on these gels under differentiation conditions, we observed a strong correlation of cationic charge concentration with NSPC survival. In particular, neurons were preferentially formed on gels with a higher cationic charge concentration, whereas astrocytes and oligodendrocytes favored weakly charged or even neutral gel surfaces. To test the properties of the gels under proliferative conditions, the NSPCs were cultivated in the presence of fibroblast growth factor 2 (FGF2). The cytokine significantly increased the number of NSPCs but delayed the differentiation toward neurons and glia cells. Thus, the hydrogels are compatible with the survival, expansion, and differentiation of NSPCs and may be useful to create supportive environments in transplantation approaches.

Acrylates in artificial nails-Results of product analyses and glove penetration studies.

Artificial nail materials are mixtures that are prone to contain several sensitizing (meth)acrylates. It is not known whether the listing of (meth)acrylates is correct in these products' packages. Protective gloves suited for nail work are needed. To analyse (meth)acrylates in gel nail and acrylic nail products chemically and to compare the results with the information in the product labels, and to study penetration of artificial nail materials through selected disposable gloves. We analysed 31 gel nail products and 6 acrylic nail products for their (meth)acrylate content by gas chromatography-mass spectrometry (GC-MS). We tested the penetration of two nail products through three disposable gloves: nitrile rubber, neoprene rubber and polyvinyl chloride (PVC). Altogether 32/37 products contained (meth)acrylates. In all of them, there was discrepancy between the listed (meth)acrylates and those discovered in the analysis. The commonest (meth)acrylates were hydroxyethyl methacrylate (HEMA, 20/37 samples) and hydroxypropyl methacrylate (HPMA, 9/37 samples), but many of the product packages failed to declare them. Isobornyl acrylate (IBA) was discovered in nine gel nail products. The neoprene glove could withstand nail gel for 20 min and thin nitrile glove and PVC glove for 5 min. Acrylic nail liquid penetrated through disposable gloves quickly. Labelling of artificial nail products was notably incorrect on most products. Requirements for product labelling must be updated so that the risk of sensitization associated with artificial nail products is clearly indicated. Disposable gloves can probably be used short-term in gel nail work, whereas disposable gloves do not protect the user from acrylic nail liquids.

Preparation of water swellable rubber from epoxidized natural rubber and sodium acrylate by in‐situ polymerization: Effect of vulcanization system, epoxide, and dicumyl peroxide, and sodium acrylate content

AbstractWater swellable rubber (WSR) was prepared from epoxidized natural rubber (ENR) and sodium acrylate (NaAA) by in‐situ polymerization using sulfur and dicumyl peroxide (DCP) as a vulcanizing agent and an initiator, respectively. The ENR, NaAA, and other additives were mixed in an internal mixer and a two‐roll mill. The effect of the vulcanization system, epoxide, and DCP, and NaAA content on the vulcanization, physical, and mechanical properties of WSR were investigated in this research. As the results, the scorch and curing time of WSR compounded with ENR 25 and vulcanized with a mixture of sulfur‐peroxided or mixed vulcanization system were less than other systems. Furthermore, the scorch and curing time decreased with the increase in DCP content. The WSR with ENR 50 vulcanized with DCP (1.5 phr) in the mixing system provided the highest tensile strength. However, the volume change of WSR with the mixing system (WSR/M) was lower than the WSR cured with peroxide (WSR/P). For WSR/P, the tensile strength, hardness, and volume change in water increased with increasing DCP, and NaAA content, while the elongation at break decreased. These results suggest that WSR has the potential for diverse applications, including waterproofing and sealing solutions in civil construction projects.Highlights Water swellable rubber (WSR) was prepared from epoxidized natural rubber (ENR) and sodium acrylate (NaAA) by in‐situ polymerization using sulfur and dicumyl peroxide (DCP) as a vulcanizing agent and an initiator. The scorch and curing time of WSR compounded with ENR 25 and vulcanized with a mixed vulcanization system were less than those of other systems. During the vulcanization process, ENR 50 can be generated by the ring‐opening of the adjacent epoxide groups more than ENR 25, and the self‐crosslink of ENR 50 was higher than ENR 25. Water swelling and volume change of WSR tended to decrease with increasing epoxide, and DCP content, whereas those properties increased with increasing NaAA content. Tensile strength, elongation at break, and hardness of WSR with the mixing system (WSR/M) were higher than those of WSR with the peroxide system (WSR/P). Swelling and volume change of WSR/P were higher than those of WSR/M.

Study on properties of Portland cement-sulfoaluminate cement-based grouting materials modified by in-situ polymerization of calcium acrylate

To enchance the toughness of ordinary Portland cement-sulfoaluminate cement-based grouting material and minimize the secondary damage of road structure caused by stone body destruction under vehicle load. In this paper, the development laws of setting time, fluidity, and mechanical strength of grouting material, and the characteristics of stone damage under the action of calcium acrylate are systematically analyzed. The mechanism by which in-situ polymerization of improves the toughness improvement of ordinary Portland cement-sulfoaluminate cement-based grouting material is then revealed. In-situ polymerization of calcium acrylate delays the setting time, and an appropriate calcium acrylate content improves the flowability. The addition of calcium acrylate largely enhances the mechanical strength of the stone body, improving the 1-day compressive strength and flexural strength by 279.18% and 301.64%, respectively. Calcium acrylate also increases the flexural compression ratio of the stone body. The highest flexural compression ratio at 28d is 0.5592. The microscopic analysis reveals that calcium acrylate promotes hydration, and forms stable calcium polyacrylate in the stone body, which connects the hydration products into a more densely cement-calcium polyacrylate composite structure. Consequently, the toughness of the stone body improves. By analyzing the stress–strain curve, the stone body still exhibits a capacity to resist damage after the peak stress under the action of calcium acrylate. Finally, a damage constitutive equation of the stone body with different damage factors is established, which has excellent agreement with the test curve and can predict the mechanical properties of cement-based grouting material modified by in-situ polymerization of calcium acrylate. The findings provide a theoretical framework for designing the strength of grouting materials and evaluating road stability.

Mechanical Properties' Strengthening of Photosensitive 3D Resin in Lithography Technology Using Acrylated Natural Rubber.

Acrylated natural rubber (ANR) with various acrylate contents (0.0-3.5 mol%) was prepared from natural rubber as a raw material and then incorporated with commercial 3D resin to fabricate specimens using digital light processing. As a result, the utilization of ANR with 1.5 mol% acrylate content could provide the maximum improvement in stretchability and impact strength, approximately 155% and 221%, respectively, over using pure 3D resin, without significant deterioration of tensile modulus and mechanical strength. According to evidence from a scanning electron microscope, this might be due to the partial interaction between the dispersed small rubber particles and the resin matrix. Additionally, the glass-transition temperature of the 3D-printed sample shifted to a lower temperature by introducing a higher acrylate content in the ANR. Therefore, this work might offer a practical way to effectively enhance the properties of the fundamental commercial 3D resin and broaden its applications. It also makes it possible to use natural rubber as a bio-based material in light-based 3D printing.

Development of protective coating system using natural rubber – acrylic polyol resin for mild steel

Purpose The purpose of this study is to develop a protective coating system on mild steel panel incorporating epoxidized natural rubber with acrylic polyol resin. Design/methodology/approach In this work, a novel attempt is made to develop binder coatings using epoxidized natural rubber-based material and an organic resin (acrylic resin) for corrosion protection on metal substrate. Seven different samples of multifunctional coatings are developed by varying the compositions of epoxidized natural rubber (ENR) and acrylic resin. The properties of the developed coatings have been characterized using analytical methods such as Fourier transform infrared spectroscopy (FTIR) and electrochemical impedance spectroscopy (EIS). EIS has been carried out for 30 days to evaluate the corrosion resistance after immersing into 3.5 wt.% of sodium chloride. Cross hatch cut tester (CHT) has been used to study the adhesive properties. UV–Visible Spectroscopy (UV–Vis) was also used to assess changes in the coating-film transparency of the natural rubber-based coating systems in this study. Findings The developed coatings have formed uniform layer on the substrate. CHT results show excellent adhesion of the coatings. Higher concentrations of ENR have higher transparency level, which reduces when the acrylic concentration increases. FTIR analysis confirms the crosslinking that occurred between the components of the coatings. Based on the impedance data from EIS, the incorporation of natural rubber can be an additive for the corrosion protection, which has the coating resistance values well above 108Ω even after 30 days of immersion. Practical implications The blending method provides a simple and practical solution to improve the strength and adhesion properties of acrylic polyol resin with epoxidized natural rubber. There is still improvement needed for long-term applications. Originality/value The work has been conducted in our laboratory. The combination of natural rubber-based materials and organic resins is a new approach in coating research.

Improving the Anti-washout Property of Acrylate Grouting Material by Bentonite: Its Characterization, Improving Mechanism, and Practical Application.

Acrylate is a popular polymer grouting material that has been widely used to control groundwater seepage. However, the vulnerability of acrylate slurry to dynamic water washout restricts its application in groundwater environments characterized by high flow velocity and water pressures. In this paper, lithium bentonite (Li-B) was used to modify the traditional magnesium acrylate (AC) grouting material. The influence of Li-B to AC ratios on the modified materials' washout resistance was explored, and the modification mechanism was analyzed using X-ray diffraction (XRD), infrared spectroscopy (IR), and scanning electron microscopy (SEM). Finally, the anti-washout ability of the modified slurry was verified through engineering applications. Results revealed that LiB-AC grout had adjustable setting times (10.5 to 395.6 s), minimal bleeding (0.1%), higher viscosity (65 mPa·s) and expansibility (350%), stronger anti-water dispersibility (24 times that of pure AC slurry), higher mechanical strength (compressive strength is 0.386 MPa, tensile strength is 0.088 MPa), and better impermeability (2.23 × 10-8 m/s). The lithium bentonite was beneficial to the setting time, bleeding, viscosity, slurry retention rate, impermeability, and mechanical strength of the acrylate grout. However, it diminished the expansibility of the acrylate grout. At the optimal acrylate content (20%), the mechanical strength and impermeability of the LiB-AC grout were the highest. The better performance of LiB-AC grout was attributed to the formation of a more stable and dense interlaced spatial network structure after the modification by Li-B. The LiB-AC grout was used in the dynamic water grouting project of a metro shield tunnel segment and achieved better anti-washout performance than cement-water glass and pure AC slurry.

Thermoresponsive Shape-Memory Biobased Photopolymers of Tetrahydrofurfuryl Acrylate and Tridecyl Methacrylate.

A series of thermoresponsive shape-memory photopolymers have been synthesized from the mixtures of two biobased monomers, tetrahydrofurfuryl acrylate and tridecyl methacrylate, with the addition of a small amount of 1,3-benzendithiol (molar ratio of monomers 0-10:0.5:0.03, respectively). Ethyl (2,4,6 trimethylbenzoyl) phenylphosphinate was used as photoinitiator. The calculated biorenewable carbon content of these photopolymers was in the range of (63.7-74.9)%. The increase in tetrahydrofurfuryl acrylate content in the photocurable resins resulted in a higher rate of photocuring, increased rigidity, as well as mechanical and thermal characteristics of the obtained polymers. All photopolymer samples showed thermoresponsive shape-memory behavior when reaching their glass transition temperature. The developed biobased photopolymers can replace petroleum-derived thermoresponsive shape-memory polymer analogues in a wide range of applications.

Influence of Alkyl Acrylate Nature on Rheological Properties of Polyacrylonitrile Terpolymers Solutions, Spinnability and Mechanical Characteristics of Fibers.

The influence of alkyl acrylate comonomers in the rank of methyl- (MA), butyl- (BA), ethylhexyl- (EGA), and lauryl- (LA) in ternary copolymers based on acrylonitrile, alkyl acrylate and acrylamide (PAN-alkyl acrylate) on their solutions rheological behavior in dimethyl sulfoxide (DMSO), and mechanical properties of the spun fibers have been investigated. To reveal the role of molecular weight, two series of copolymers with molecular weights of ~50 and 150 kg/mol have been studied. It was shown that the nature of the alkyl acrylate does not significantly affect the rheological behavior of their solutions regardless of the length of the alkyl substituent and the content of the alkyl acrylate in copolymers. An exception is the high-molecular PAN-LA, which is characterized by a non-Newtonian behavior at lower concentrations. Two series of fibers were spun from the characterized ranks of low and high-molecular-weight copolymer solutions. For all copolymers, a 2.5-5-fold increase in the strength and elastic modulus of the fiber was found with an increase in Mw. It has been shown that PAN-MA and PAN-LA fibers have a tensile strength of 800 MPa that is 1.5-3 times higher than that of other copolymers spun in the same conditions.

Synthesis of photoactive nanocomposite hydrogels via in-situ photoinitiated thiol-ene click polymerization of acrylates containing norbornene-POSS and norbornene-POSS/Ag NPs

Radical-mediated thiol-ene photopolymerization is a method that has been studied intensively since the beginning of the century due to the nature of click chemistry which can be carried out in a fast, controllable, and easy way under mild environment conditions with no or minimal formation of by-products. In order to improve the properties of the polymeric nanocomposite materials which have been obtained by photopolymerization method and to prepare them for a particular purpose, various nano-sized photo-reactive groups or cross-linking agents have been added to the formulations. The advantage of this study for the preparation of thin-film and hydrogel nanocomposites is based on one-pot thiol-ene photo-click polymerization. The main contribution made by one-component Type II photoinitiator, 2-Mercaptothioxanthone (TX-SH) carries both thiol functionality and chromophoric group on it. Polyhedral oligomeric silsesquioxane (POSS) functionalized with 1 or 3 norbornene units was used as alkene and played a good role in the preparation of nanocomposite hydrogels with/without in-situ formed silver nanoparticles (Ag NPs) with various acrylate content by thiol-ene photo-click polymerization. Especially the good contribution of norbornenylethyl disilanol isobutyl polyhedral oligomeric silsesquioxane (1NBPOSS) or tris-norbornenyl isobutyl polyhedral oligomeric silsesquioxane (3NBPOSS) was seen in terms of conversion percentage of acrylates which was determined by photo differential scanning calorimetry (photo-DSC) and swelling ratios of hydrogels in phosphate buffer solution (PBS) buffer solution. Besides them, obtained nanocomposites displayed good thermal stability values according to the Thermogravimetric analysis (TGA) measurements and scanning electron microscopy (SEM) images confirmed rather small-sized and uniform in-situ formed Ag NPs.

New Pressure-Sensitive Acrylic Adhesives for Low Energy Substrates Prepared via UV-Induced Telomerization with a Fluorine-Based Telogen

Novel pressure-sensitive adhesives (PSA) for low energy substrates were prepared by a solvent-free UV-initiated telomerization process using n-butyl acrylate, butyl methacrylate, and lauryl methacrylate (LMA), with trifluoroethanol (TFEtOH) as a telogen, and acylphosphine oxide (APO) as a radical photoinitiator. A crosslinking monomer (an aliphatic urethane acrylate, L9033) and a radical UV-photoinitiator (α-hydroxyalkylphenone) were also tested as components of the adhesive compositions. The influence of LMA and TFEtOH on the UV-phototelomerization process kinetics and the physicochemical features of the obtained fluorotelomers, as well as the concentration of L9033 on the PSA adhesion to a polyethylene surface, were investigated. FT-IR results indicated that the fluorine groups were successfully introduced into the telomer structure. The highest adhesion relative to a polyethylene substrate (12.3 N/25 mm), and the highest hydrophobicity (with a contact angle of 95° for a water/PSA system) were observed for adhesives based on a telomer syrup containing 5 wt. parts of TFEtOH and 30 wt. parts of LMA (per 100 wt. parts of the monomer mixture). Additionally, it was revealed that a higher aliphatic urethane acrylate content and a higher UV dose increased the adhesion feature.

Optical and Electrical Characterization of Polymer Dispersed Nematic Liquid Crystals

Polymer dispersed liquid crystals are composite functional materials having a variety of application ranging from display to smart window. These materials consist of liquid crystal in which micron size droplets of polymer is dispersed. In the present study the effect of different concentration of polymer 2-ethyl hexyl acrylate on optical and electrical properties of nematic liquid crystal 4-cynophenyl 4-n-hexyl benzoate were investigated by various techniques. The investigation of textures at different temperatures was performed by polarizing optical microscopy for the determination of phase transition temperature. The fabry perot scattering studies using low powered laser beam was used for the confirmation of phase transition temperature. Various textures were found according to the orientation of liquid crystal and polymer. The optical and electrical properties of pure liquid crystal were found to enhance after dispersing polymer. Our investigation suggest that after dispersing polymer into nematic liquid crystal, the material shows more stability, less flicking and sticking of image for display applications.

Optimization of synthesis conditions for preparation of radiation grafted polymeric fibers and process variables of adsorption with response surface methodology

Radiation-grafted polymeric adsorbents have a high adsorption capacity in purifying effluents from heavy metals. This study investigated adsorption conditions for removing uranium from aqueous nitrate solution using radiation-grafted polymeric adsorbent (PP-g-(PAAc-co-PAm)). The modified fiber (polypropylene) was synthesized with acrylic amide and acrylic acid monomers. The central composite design approach in two stages was used to determine optimal conditions. In the first stage, the effects of three factors such as acrylic amide concentration, sulfuric acid concentration and dose of gamma-ray on adsorbent synthesis were investigated to prepare an appropriate adsorbent. The impacts of three parameters, including the initial aqueous pH, uranium ion concentration, and equilibrium time on adsorption conditions, were studied using a central composite approach in the second stage. The optimum conditions for sulfuric acid concentration, acrylic amide concentration, the dose of gamma-ray, initial aqueous pH, uranium concentration, and time were optimized equally to 59.7% (v/v), 0.08 M, 20 kGy, 7, 80 ppm, and 3 h, respectively. The uranium adsorption yields equal to 62.04% achieved from the quadratic equation agreed with the experimental value equal to 59.07%. The uranium adsorption was attained to 16.79 mg/g with a grafting percentage of 30.58% under the optimum conditions. Kinetics and equilibrium isotherms described experimental data following pseudo-second-order and Langmuir models. Finally, the results showed that the radiation-grafted polymeric adsorbents are effective in uranium uptake from effluents.

Antimicrobial dual‐cured photopolymers of vanillin alcohol diglycidyl ether and glycerol dimethacrylate

AbstractConsidering the current efforts for to develop new antimicrobial polymers from renewable resources suitable for application in environmentally friendly light‐based technologies, novel dual‐cured photopolymers of vanillin alcohol diglycidyl ether and glycerol dimethacrylate are developed. The kinetics of the sequential and simultaneous dual‐curing processes, combining free radical and cationic photopolymerizations, is investigated by real‐time photorheometry. Comparison of dual‐curing systems with different ratios of biobased epoxy and acrylate monomers revealed that the increase in the acrylate content increases the photocuring rate and improves the mechanical performance (Young's modulus increases from 76.64 to 190.71 MPa) and thermal stability (the 10% weight loss increases from 227 to 274°C) of the polymers, while the increase in the vanillin epoxy content results in better antimicrobial activity. Developed photopolymers create unfavorable conditions for the growth of microorganisms and reduce their population by up to 0% in 24 h. The excellent antibacterial and antifungal activity of new photopolymers allows them to be considered as biobased alternatives to petroleum‐based antimicrobial coatings, films, or optical 3D printed objects.

Digital Light Processing 3D-Printed Silica Aerogel and as a Versatile Host Framework for High-Performance Functional Nanocomposites.

Vat-photopolymerization-based 3D printing enables on-demand construction of customized objects with scalable production capacity and high precision. Herein, the sol-gel process for aerogels with digital light processing 3D printing to produce advanced functional materials possessing hierarchical pore structures and complex shapes is combined. It has revealed the temporal evolution of the photorheological behavior of acrylate-modified silica sols in an acid-base catalytic procedure, and confirmed that silica aerogels can be fabricated with very low acrylate content. The resulting aerogels are thermostable with intrinsic silica contents, skeletal densities, and physical characteristics similar to those of commercial silica aerogels yet distinct mechanical behaviors. More importantly, the printed silica aerogels can be used as a versatile nanoengineering platform to produce high-performance and multifunctional interpenetrating phase nanocomposites with complex shapes through programmable post-printing processes. Epoxy-based nanocomposites possessing excellent mechanical performance, ionogel-based conductive nanocomposites with decoupled electrical and mechanical properties, and anti-swelling hydrogel-based nanocomposites are demonstrated. The results of this study offer new guidelines for the design and fabrication of novel materials by additive manufacturing.