Diethylene Glycol Diacrylate Research Articles

Functionally Modified Polymer Electrolyte Based on Noncovalent Interaction for Stable Lithium Metal Batteries.

The charge transfer efficiency of the solid electrolyte depends on the number of lithium ions that can be effectively transported and participate in the electrode reaction. However, limited by the strong coupling relationship between Li+ and Lewis basic sites on the polymer chain, the Li+ transference number (tLi+) of the solid polymer electrolyte (SPE) based dual-ion conductor is typically low, resulting in excessive anion aggregation at the electrode side and inducing concentration polarization. In this study, we present a functionalized modified polymer electrolyte (FMPE) with selective cation transport, which was synthesized by embedding 4-(trifluoromethyl)styrene (TFS) functionalized groups onto the poly(diethylene glycol diacrylate) polymer chain. The TFS group formed noncovalent couplings with TFSI- anions through hydrogen bondings and dipole-dipole interactions, which effectively limited the migration of the anions and contributed to the elevated tLi+ of the FMPEs to 0.595 and 0.699 at 25 and 60 °C, respectively. Density functional theory (DFT) calculations were performed to verify the increased anion migration barriers for different noncovalent interactions and revealed that the conjugated system formed by the delocalized π electrons of the benzene ring and the C═O groups helped to disperse the electron distribution of the polymer chains. Consequently, the decrease in the degree of Li+ immobilization promotes the decoupling and migration of Li+ between the polymer chains. Benefiting from optimized Li+ transport behavior, the lithium metal batteries (LMBs) assembled by FMPEs and LiFePO4 exhibit excellent rate performance (discharge specific capacity of 88.8 mAh g-1 at 5 C) and stable long-term cycle performance (capacity decay rate of only 0.064% per cycle for 500 cycles at 25 °C and 0.5 C).

Synthesis and Characterisation of 4D-Printed NVCL-co-DEGDA Resin Using Stereolithography 3D Printing

The design and manufacturing of objects in various industries have been fundamentally altered by the introduction of D-dimensional (3D) and four-dimensional (4D) printing technologies. Four-dimensional printing, a relatively new technique, has emerged as a result of the ongoing development and advancements in 3D printing. In this study, a stimulus-responsive material, N-Vinylcaprolactam-co-DEGDA (NVCL-co-DEGDA) resin, was synthesised by Stereolithography (SLA) 3D printing technique. The N-Vinylcaprolactam-co-DEGDA resins were initiated by the Diphenyl (2,4,6-trimethylbenzoyl) phosphine oxide (TPO) photoinitiator. A range of Di(ethylene glycol) diacrylate (DEGDA) concentrations in the NVCL-co-DEGDA resin was explored, ranging from 5 wt% to 40 wt%. The structural properties of the 3D printed objects were investigated by conducting Attenuated Total Reflectance–Fourier Transform Infrared Spectroscopy (ATR-FTIR). Additionally, the 3D printed samples underwent further characterisation through differential scanning calorimetry (DSC) and swelling analysis. The results revealed an inverse relationship between DEGDA concentration and Tg values, indicating that higher concentrations of DEGDA resulted in lower Tg values. Additionally, the pulsatile swelling studies demonstrated that increasing DEGDA concentration prolonged the time required to reach the maximum swelling ratio. These findings highlight the influence of DEGDA concentration on both the thermal properties and swelling behaviour of 3D printed samples.

The Effect of Silane Acrylate Containing Ethylene Glycol Chains on the Adhesive Performance and Viscoelastic Behavior of Acrylic Pressure-Sensitive Adhesives for Flexible Displays.

In this study, novel silane acrylates, such as diethylene glycol diacrylate (DEGDA) and tetraethylene glycol diacrylate (TEGDA), containing ethylene glycol chains were synthesized and introduced into acrylic pressure-sensitive adhesives (PSAs) to regulate their peel strength and rheological properties. The synthesized silane acrylates effectively improved the cohesion and adhesive properties of the acrylic PSAs, even with only 1 wt% addition. In addition, the glass transition temperature and flexibility of acrylic PSAs were also affected by the increase in free volume induced by ethylene glycol chains. The silane acrylates also improved the viscoelasticity of the acrylic PSAs, which exhibited excellent recovery (62-96%) and stress relaxation (>90%) properties owing to the increased elasticity. Additionally, the acrylic PSAs prepared with the silane acrylates showed excellent optical properties (transmittance ≥ 90%, haze ≤ 1%) and exhibited behavior suitable for application in flexible displays from a comprehensive perspective.

Synthesis and Characterisation of Hydrogels Based on Poly (N-Vinylcaprolactam) with Diethylene Glycol Diacrylate.

Poly (N-vinylcaprolactam) is a polymer that is biocompatible, water-soluble, thermally sensitive, non-toxic, and nonionic. In this study, the preparation of hydrogels based on Poly (N-vinylcaprolactam) with diethylene glycol diacrylate is presented. The N-Vinylcaprolactam-based hydrogels are synthesised by using a photopolymerisation technique using diethylene glycol diacrylate as a crosslinking agent, and Diphenyl (2, 4, 6-trimethylbenzoyl) phosphine oxide as a photoinitiator. The structure of the polymers is investigated via Attenuated Total Reflectance-Fourier Transform Infrared Spectroscopy. The polymers are further characterised using differential scanning calorimetry and swelling analysis. This study is conducted to determine the characteristics of P (N-vinylcaprolactam) with diethylene glycol diacrylate, including the addition of Vinylacetate or N-Vinylpyrrolidone, and to examine the effects on the phase transition. Although various methods of free-radical polymerisation have synthesised the homopolymer, this is the first study to report the synthesis of Poly (N-vinylcaprolactam) with diethylene glycol diacrylate by using free-radical photopolymerisation, using Diphenyl (2, 4, 6-trimethylbenzoyl) phosphine oxide to initiate the reaction. FTIR analysis shows that the NVCL-based copolymers are successfully polymerised through UV photopolymerisation. DSC analysis indicates that increasing the concentration of crosslinker results in a decrease in the glass transition temperature. Swelling analysis displays that the lower the concentration of crosslinker present in the hydrogel, the quicker the hydrogels reach their maximum swelling ratio.

Quasi-Solid Polymer Electrolyte with Multiple Lithium-Ion Transport Pathways by In Situ Thermal-Initiating Polymerization.

Solid polymer electrolytes (SPEs) are considered to be attractive candidates for rechargeable batteries on account of their high safety and flexible processability. However, the restricted polymer segmental dynamics limit the Li+ conduction of SPEs. Herein, a composite electrolyte membrane was prepared via in situ thermal-initiating polymerization of diethylene glycol diacrylate (DEGDA) in a poly(vinylidene fluoride) frameworks (PVDF FMs) electrospun in advance. As a quasi-solid polymer electrolyte (QSPE), it provides multiple transport highways for Li+ built by the C═O or C-O or C═O/C-O groups in poly(diethylene glycol) diacrylate (PDEGDA), respectively, proved by density functional theory calculations together with the high-resolution 7Li solid-state nuclear magnetic resonance spectra. Since the interaction between Li+ and C═O is weaker than that between Li+ and C-O, Li+ tends to move along C═O dominating paths in PDEGDA/PVDF FMs QSPEs, even skipping back to C═O nodes from the original C-O dominating way. Multiple transport patterns facilitate Li+ migration within PDEGDA/PVDF FMs QSPEs, contributing to the ionic conductivity of 1.41 × 10-4 S cm-1 at 25 °C and the Li+ transference number of 0.454. Ascribing to the wetting capability of the monomer to the electrodes in use, compatible electrolyte/electrode interfaces with low interface resistance and compact cells were acquired by the in situ polymerization. Protective lithiated oligomers (RCOOLi) and LiF are enriched at the Li anode surface, promoting a lasting stable Li plating/stripping over 2000 h. By applying the QSPEs in LiFePO4 cell, a capacity of 157.7 mAh g-1 with almost 100% coulombic efficiency during 200 cycles is achieved at 25 °C.

Enhanced thermal and mechanical properties of 3D-printed PEG containing acrylate composite with surface-treated BN via digital light processing

The interest in additive manufacturing technology of 3D printed composite is increasing owing to its potential applications with a wide variety of shapes and properties. Through digital light processing (DLP), the polymer-based thermally conductive composites with phase change material for heat management were fabricated. Diethylene glycol diacrylate (DEGDA), polyethylene glycol (PEG), and phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide (BAPO) were selected as a monomer, oligomer, and photo-initiator for UV curable resins. Boron nitride was hydroxylated and grafted with PEG to improve the interfacial interaction between the filler and the matrix. Optimization of DLP parameters such as light intensity, exposure time, and operating temperature was performed to enhance the quality of the 3D-printed composite. The resulting composite exhibited a thermal conductivity of 0.916 W/(m·K) and mechanical strength of 7.36 MPa, which are 216% and 167% higher than those of the respective matrices. Moreover, the composite has a latent heat of 200.22 J/g. The advantages of the 3D-printed polymer-based phase change material composite for advanced electronic packaging were explored. This study opens a new era in the fabrication of organic PCMs with enhanced thermal conductivity via digital light processing.

Oxidative Degradation of Thermosets Based on Thioketal Cleavable Linkages in Aqueous Environment

Thermosets are rigid, infusible, and unmolded materials containing three-dimensional (3D) cross-linked structures. They are considered a fundamental pillar in the international economy, which are produced by 65 million tons annually. The responsive cross-linking moieties provide the thermosets characterized with outstanding physicochemical properties such as stiffness, degradability, and chemical and thermal resistance. We prepared degradable thermoset materials using thioketal (TK) cross-linkers, which underwent main-chain or side change degradation in the presence of hydrogen peroxide in water. TK cross-linkers at different concentrations (5, 10, and 20% wt %) were polymerized with 2-hydroxyethyl acrylate (HEA) or with 2-hydroxyethyl methacrylate (HEMA) and 1-vinyl-2-pyrrolidone (PD) to produce cross-linked poly(HEA) and poly(HEMA-PD) by free radical polymerization, respectively. The resultant polymer materials completely degraded in hydrogen peroxide/water (3–30%, vol). Using isophorone diisocyanate, we also produced degradable polyurethane based on TK-bearing diol. We prepared a 3D degradable thermoset using the Direct-Ink-Writing (DIW) 3D printing technology, which was charged by diethylene glycol diacrylate (15%, wt %) and a prepolymer (isophorone diisocyanate terminated by acrylate moieties) containing diol-thioketal linkage (15%, wt %). Finally, we found that TK-poly(HEA) underwent microbial degradation by Lactobacillus jensenii at 37 °C, which indicates a benign eco-friendly effect.

4D Printing of Smart Polymer Nanocomposites: Integrating Graphene and Acrylate Based Shape Memory Polymers.

The ever-increasing demand for materials to have superior properties and satisfy functions in the field of soft robotics and beyond has resulted in the advent of the new field of four-dimensional (4D) printing. The ability of these materials to respond to various stimuli inspires novel applications and opens several research possibilities. In this work, we report on the 4D printing of one such Shape Memory Polymer (SMP) tBA-co-DEGDA (tert-Butyl Acrylate with diethylene glycol diacrylate). The novelty lies in establishing the relationship between the various characteristic properties (tensile stress, surface roughness, recovery time, strain fixity, and glass transition temperature) concerning the fact that the print parameters of the laser pulse frequency and print speed are governed in the micro-stereolithography (Micro SLA) method. It is found that the sample printed with a speed of 90 mm/s and 110 pulses/s possessed the best batch of properties, with shape fixity percentages of about 86.3% and recovery times as low as 6.95 s. The samples built using the optimal parameters are further subjected to the addition of graphene nanoparticles, which further enhances all the mechanical and surface properties. It has been observed that the addition of 0.3 wt.% of graphene nanoparticles provides the best results.

An ultraviolet-assisted electrospinning procedure of polyimide ultrafine fibrous membranes fabricated by ester-type negative photosensitive polyimide

An ultraviolet-assisted electrospinning (UVAES) procedure was performed using in situ photopolymerization during the electrospinning process to enhance the solvent resistance of polyimide (PI) ultrafine fibrous membranes (UFMs). The resultant PI UFMs were fabricated via solution electrospinning using photosensitive poly(amic acid ester) (PSPAE) modified with unsaturated double bond side chains as the main fiber-forming agent, diethylene glycol diacrylate as the crosslinker, and titanocene as the photoinitiator. The precursor PSPAE UFMs were prepared via both of normal electrospinning and UVAES procedures and then were converted to PI using thermal imidization at 350 °C in a nitrogen imidization. The physical and chemical properties of the obtained PI UFMs were subsequently studied. The fibers exposed to ultraviolet irradiation possessed a smooth surface morphology and maintained their fibrous structure after thermal imidization at elevated temperature as high as 350 °C in nitrogen, whereas the crosslink-free PSPAE fibers lost their fibrous structure after heating. Furthermore, as well as providing enhanced thermal decomposition stability, the introduction of a crosslinked structure via ultraviolet irradiation also protected the molecular chains from organic solvents, resulting in excellent solvent resistance of the PI UFMs.

Synthesis and characterization of hydrogels containing redox‐responsive 2,2,6,6‐tetramethylpiperidinyloxy methacrylate and thermoresponsive N‐isopropylacrylamide

AbstractSmart hydrogels containing 2,2,6,6‐tetramethylpiperidinoxy methacrylate (TEMPO) and N‐isopropylacrylamide (NIPAM) that undergo reversible redox behavior are prepared and investigated. Several polymer networks are first prepared by free‐radical copolymerization of varying amounts of TEMPO, NIPAM, and a crosslinker (diethylene glycol diacrylate) and subsequently swelled with water to lead to hydrogels. In order to investigate the effects of the redox activity of TEMPO units and of the lower critical solution temperature of NIPAM on the hydrogel properties, a study of the swelling ratio of the polymer networks in distilled water at different temperatures is performed for the two forms of TEMPO, the reduced (TEMPO) and oxidized (TEMPO+) one. Moreover, the rheological properties are also measured for both hydrogel forms. Finally, the encapsulation abilities of the oxidized hydrogels are demonstrated via electrostatic interactions between positively charged TEMPO+ units and negatively charged guest molecules, supporting future application of our system in the biomedical and environmental fields.

Radiation Synthesis of Molecularly Imprinted Hydroxyethylmethacrylate-based Matrices for Glucose Recognition

I n this study, 2-hydroxyethyl methacrylate (HEMA) was used as functional monomer and diethylene glycol diacrylate (DEGDA) and polyethylene glycol (200) diacrylate (PEG(200)DA) were used as crosslinking agents to imprint D(+)glucose. D(+)glucose imprinted polymers were prepared in the presence of dimethyl sulfoxide (DMSO) /isopropyl alcohol (IPA) (3/1, v/v) at room temperature, in the air by radiation-induced polymerization/ crosslinking. The control polymers were synthesized by the same procedure in the absence of D(+)glucose. In order to evaluate the recognition and separation properties of the imprinted system high performance liquid chromatography (HPLC) experiments were carried out where β (-) lactose, D(+)glucose and glycerol were used as analytes. To increase the affinity of the template to the stationary phase polarity of the mobile phase was decreased by the addition of acetonitrile into water. Optimum composition of acetonitrile/water (1/5 v/v) was determined according to the swelling experiments. The sizes of the cavities in the polymeric networks were determined by positron annihilation lifetime spectroscopy (PALS). The average radii of cavities were found as 0.254 and 0.279 nm for freeze-dried imprinted polymers prepared by using PEG(200)DA after swollen in water and acetonitrile/water mixture (1/5 by volume), respectively.

Effects of the methacrylate/acrylate monomers HEMA, TEGDMA, DEGDA, and EMA on the immune system.

Incomplete curing of dental fillings may lead to leakage of methacrylate/acrylate monomers, which may come in contact with different cells of the immune system in oral tissues. Very little is known about the different immunologic effects caused by these methacrylates/acrylates. The objective of the present study was to study if and how the methacrylate/acrylate monomers ethyl methacrylate (EMA) and diethylene glycol diacrylate (DEGDA) affect the immune system in vivo and in vitro in comparison to 2‐hydroxyethyl methacrylate (HEMA) and triethylene glycol dimethacrylate (TEGDMA). Human peripheral blood mononuclear cells were exposed to the different monomers (500 and 1000 μM) for 24 hr in vitro. BioPlex Pro™ assays were used for cytokine analysis. In vivo, BALB/c mice were immunized subcutaneously at the base of the tail with HEMA, TEGDMA, EMA, or DEGDA in combination with ovalbumin (OVA) in order to study adjuvant properties of the 4 monomers. Peripheral blood mononuclear cells exposed to DEGDA had viability less than 50% of the cells. A pattern was observed where the levels of most cytokines were elevated after exposure to HEMA or TEGDMA. Since that, many cells died after DEGDA‐exposure, the only observed cytokine secretion was a significantly increased production of interleukin‐18. In the in vivo experiments, all mice immunized with DEGDA died after the booster injection. Mice receiving OVA in combination with HEMA, TEGDMA, or EMA developed a higher immunoglobulin G anti‐OVA antibody levels compared to the group immunized with OVA alone. We could not demonstrate any significant difference in antibody levels among the mice receiving the various methacrylate/acrylate monomers. The different monomers affected the production, increase and decrease, of different cytokines in vitro but resulted also in vivo in increased antibody production and T‐cell activity.

Development of a metal/chelate polyhydroxyethylmethacrylate monolith capillary for selective depletion of immunoglobulin G from human plasma for proteomics

In this study, we report the development of a new poly HEMA (HEMA-co-DEGDA-co-DATD) monolith capillary functionalized with “IDA-Cu (II) complex”. Of the two tested crosslinkers (methylene bisacrylamide (MBAAm) and diethylene glycol diacrylate (DEGDA)), presence of DEGDA has enhanced the monolith rigidity. Structural assembly of these monoliths are organized with highly interconnected large globule like structures and dominated by macropore region. Iminodiacetic acid (IDA) immobilization was performed using two chemical approaches (i. aldehyde − secondary amine reaction and ii. epoxy − sec. amine reaction). FT-IR analysis confirmed successful IDA immobilization in both cases. For the first time, a reaction of sec. amine ligand with aldehyde functional material was successfully reported. Overall, the Cu (II)-IDA monolith capillary showed good permeability (3.05×10 −13m2), high IgG adsorption capacity and reusablilty even after 5 consecutive adsorption-desorption cycles. The amount of protein (IgG/HSA) adsorbed on Cu (II)-IDA monolith prepared via the two chemistries is almost similar. Using this affinity monolith capillary, we selectively depleted ∼95% of IgG from human plasma (dilution of 1:16).

A Novel Method of Copper Green Bodies Production: Through a Low Toxicity Gelling System in a Non-Aqueous Based Gelcasting Process

The importance of gelcasting process is related to producing strong de-mouldable complex shape green bodies through polymerization of monomer in colloidal suspensions. As such, research in modeling of viscosity, stability, casting, polymerization, dispersion and toxicity of colloidal suspension is of particular importance as these factors affect the resultant green bodies. The current study uses a low toxicity gelling systems based on 2-hydroxypropyl methacrylate (HPMA), 2-hydroxyethyl methacrylate (HEMA), and N,N-dimethylacrylamide (DMAA) in the synthesis of copper green bodies through a non-aqueous gelcasting process. The monomers are polymerized in 1,2-propanediol and cross-linked by diethylene glycol diacrylate to form three dimensional network structures that hold the copper particles. Viscosity, polymerization time, flexural strength, and relative density of the resultant colloidal suspension having copper particles suspension are investigated in details. Their flexural strength and density values strongly depend on optimum gelcasting process parameters and the chemical character of the monomer used.

Inkjet printing of 3D nano-composites formed by photopolymerization of an acrylate monomer

This paper considers inkjet printing of optical quality 3D nano-composites from diethylene-glycol diacrylate monomer (DEGDA) containing ZrO2 nanoparticles at varying concentrations. One application for the composites is for gradient refractive index (GRIN) lenses. The process involves printing of a nanoparticle loaded monomer “ink” onto a substrate and then photopolymerizing the monomer layer by layer using UV light. The results of the study confirm that the presence of nanoparticles favorably affects the reaction kinetics. The reaction rate and chemical conversion are enhanced considerably by the nanoparticles. A seamless interface between the layers, which are 20μm thick, may be achieved if the conversion level of the layer onto which ink is deposited is limited at 60 to 80%. Dynamic mechanical analysis (DMA) data indicate that both the glass transition and sub Tg viscoelastic properties are influenced by the nanoparticles. When nanoparticles are introduced the Tg relaxation shifts to lower temperatures and a sub Tg relaxation appears whose intensity increases with particle concentration. These results are consistent with a molecular confinement model involving a lower crosslink density rubbery layer at the polymer–particle interfaces.

Effects of nanoparticles on photopolymerization of acrylate monomers in forming nano-composites

The UV photopolymerization of diethylene glycol-diacrylate and isobornyl-acrylate based nano-composites was studied with respect to reaction conversion with variations in UV light exposure. The composites contained various amounts of well dispersed ZrO2 nanoparticles. The degree of conversion achieved vs light intensity was measured by DSC for various compositions ranging from 0 to 30% by weight of nanoparticles. It was found that including nanoparticles in the monomer increased the conversion achieved considerably. This is attributed to the acceleration of the reaction through interactions with the silane surface ligand on the nanoparticles. The upper limit for conversion was limited because of vitrification and was different for each monomer. Also noted was that the detailed effects of particle concentration on conversion are quite different for the two monomers. Conversion vs UV exposure data such as those presented provide information necessary for determining the appropriate UV exposure required for creating nano-composites by inkjet printing with optimized physical, mechanical, and optical properties. The results indicate that it is important to determine this information for forming nano-composites from any specific monomer/nanoparticle combination.

Facile eco-friendly synthesis of 3,4,6,7-tetrahydro-3,3,6,6-tetramethyl-2H-xanthene 1,8(5H,9H)-dione, crystal structure and theoretical study

New biologically active coumarin derivative, substituted xanthene-dione was synthesized by an easy, facile, cost-effective and efficient method from dimedone and diethylene glycol diacrylate without use of expensive and hazardous catalyst. The synthesis is simple, short, high-yielding and moreover does not require expensive solvents. The compound was characterized by IR, NMR and X-ray crystallography study. DFT (Density Functional Theory) calculations were performed at Becke’s three-parameter functional and Lee-Yang-Parr functional (B3LYP) level of calculation and the 6-31G++ basis set was used for ground state geometry optimization. A comparison of the selected bond lengths and bond angles of the crystal structure and theoretically optimized structure by DFT have shown good agreement. The DFT study of electron surface potential (ESP), showed a large intramolecular charge transfer efficiency of the molecule indicating optical activity of xanthene dione.

One-pot synthesis of pH-sensitive poly(RGD-co-β-amino ester)s for targeted intracellular drug delivery

We report a convenient synthetic approach for one-pot preparation of poly(β-amino ester)s copolymerized with peptides. A family of copolymers with tertiary amine groups was synthesized by copolymerizing di(ethylene glycol) diacrylate (DEDA), poly(ethylene glycol) diacrylate (PEGDA), 3-(diethylamino)propylamine (DEPA) and GGRGD peptides using the Michael addition reaction. The hydrophobic/hydrophilic properties of the resulting copolymers are adjusted by altering the feed ratios of DEDA and PEGDA. The copolymers self-assembled into nanoparticles with sizes around 60–140 nm in aqueous media, which were confirmed by dynamic light scattering (DLS) and transmission electron microscopy (TEM) techniques. The copolymers exhibit pH sensitive properties upon introduction of DEPA moieties, which were proved by pyrene fluorescence and pH titration measurements. The acid-triggered dissociation behaviors of the nanoparticles were studied by DLS and Nile red (NR) release experiments, revealing that the sizes of dissociated copolymer nanoparticles were closely relevant to their compositions. The nanoparticles can load the hydrophobic anticancer drug, i.e., doxorubicin (DOX). The DOX-loaded nanoparticles were stable in a neutral phosphate buffer solution with a payload leakage less than 20% at 37 °C. However, a significant acid-triggered DOX release was accomplished at pH 5.0 with release efficiency up to 60–80%. Because of the decoration of Arg-Gly-Asp (RGD) peptides onto the poly(β-amino ester)s, the DOX-encapsulated nanoparticles formed by poly(RGD-co-β-amino ester)s can be internalized by cancer cells via an αvβ3 integrin-mediated endocytosis pathway and accumulated in the lysosomes that provide an acidic environment to promote the release of DOX. Finally, the DOX-encapsulated copolymer nanoparticles with the targeted RGD peptide exhibited higher efficiency to kill U87 human glioblastoma cancer cells than that without RGD, which was further proved by cellular uptake of DOX-loaded nanoparticles.

Tuning biodegradable hydrogel properties via synthesis procedure

Biodegradable hydrogels have become a rapidly expanding area of research for biomedical applications. Poly(β-amino ester) (PBAE) biodegradable hydrogels, in particular, have been studied extensively because of the ease of synthesis and range of properties exhibited. In this work, PBAE macromers were created with poly(ethylene glycol) diacrylate (PEGDA), diethylene glycol diacrylate (DEGDA), and isobutylamine. Many methods have been presented that allow control over the resulting hydrogel behavior. Here, properties were varied by combining multiple diacrylate components in the macromer synthesis step (single macromer (SM)) or through the combination of multiple macromers prior to polymerization (double macromer (DM)). The exhibited properties are a result of the hydrophilic/hydrophobic contributions of the different diacrylate molecules to the macromer. The SM systems exhibited linear degradation profiles, the rate of degradation increased as the PEGDA concentration increased. DM systems exhibited a multiphase degradation profile as a result of the combination of macromers with different hydrophilic properties.

Bubble-point measurement for the CO2+diethylene glycol diacrylate and CO2+diethylene glycol dimethacrylate systems at high pressure

Pressure-composition isotherms are measured by using a static apparatus for the phase behavior data for the CO2+diethylene glycol diacrylate (DEGDA) and CO2+diethylene glycol dimethacrylate (DEGDMA) systems. The experiments are performed at five temperatures of (313.2 to 393.2) K and pressures up to 28.3 MPa. The solubility of CO2 for the two systems decreases as the temperature increases at a fixed pressure. The CO2+DEGDA and CO2+ DEGDMA systems exhibit type-I phase behavior. The experimental results for the CO2+DEGDA and CO2+DEGDMA systems are correlated with Peng-Robinson equation of state using a mixing rule.