Tripropylene Glycol Research Articles

Comparison of composite resins containing UV light-sensitive chitosan derivatives in stereolithography (SLA)-3D printers

This study produced composite resins by combining acrylate, chitosan (CH), carboxymethyl chitosan (CMCH), hydroxypropyl chitosan (HPCH), and hydroxyethyl chitosan (HECH) to create materials suitable for use in 3D stereolithography (SLA) printers. Tripropylene glycol diacrylate (TPGDA), urethane acrylate (UA), and photoinitiator (Diphenyl (2, 4, 6-trimethylbenzoyl) phosphine oxide (TPO)) were mixed. CH and its derivatives were added separately to the resin to obtain composite resins. The mechanical test results are clear; the optimum TPGDA: UA ratio was 1:1, the cure time was 60 s, and the TPO ratio was 1 %. The optimum viscosity of the resin is 340–350 cP. Hydrophobic/hydrophilic properties of cured composite resins were examined. The addition of CH and its derivatives to the resin caused a decrease in compressive strength. Adding up to 2.5 % CH, CMCH, and HECH to the resin significantly increased the tensile strength of the resin, giving it flexibility. The gel content of cured composite resins was between 97.72 % and 96.11 %. The cured composite resins demonstrated high chemical and solvent resistance to HCl, NaOH, and HF but exhibited limited resistance to toluene and chloroform. The accelerated UV aging test results show that adding CH derivatives to the resin makes the composite resin more prone to photooxidative aging.

Influence of various cleaning solutions on the geometry, roughness, gloss, hardness, and flexural strength of 3D-printed zirconia

This study aimed to investigate the impact of various cleaning solutions on the geometry, roughness, gloss, hardness, and flexural strength of 3D-printed zirconia. Cleaning solutions, including isopropyl alcohol (IPA, 99.9%), ethyl alcohol (EtOH, 99.9%), and tripropylene glycol monomethyl ether (TPM, ≥ 97.5%), were diluted to a concentration of 70% and categorized into six groups: IPA99, EtOH99, TPM97, IPA70, EtOH70, and TPM70. Zirconia discs, printed via digital light processing, were sintered after cleaning. The geometry, roughness, gloss, hardness, and flexural strength were analyzed. Statistical analysis was performed using one-way ANOVA with Tukey’s post hoc test (p < 0.05). The thickness of TPM70 was the highest. The diameter of TPM70 was significantly larger than that of EtOH99 and IPA70 (p < 0.05). The weight of the TPM groups was significantly higher than that of IPA70 (p < 0.05). The roughness Ra of TPM70 was significantly greater than that of IPA99, EtOH99, and EtOH70 (p < 0.05). The differences in surface gloss, hardness, and flexural strength among the different groups were not statistically significant (p > 0.05). Different cleaning solutions did not affect the surface gloss, hardness, and flexural strength of 3D-printed zirconia. High and low concentrations of the same cleaning solution did not affect the surface gloss, hardness, and flexural strength. IPA70, TPM97, and EtOH can be considered viable post-printing cleaning alternatives to the traditional gold standard, IPA99.

Typ‐I‐Photoinitiator auf der Basis nachhaltiger Kohlenstoffpunkte

AbstractNachhaltige Kohlenstoffpunkte, die an der Oberfläche Oximestergruppen enthalten, welche einer homolytischen Bindungsspaltung folgen, zeigen ein Potential als Photoinitiatoren für die traditionelle freie radikalische Photopolymerisation. Die Kohlenstoffpunkte wurden nach einem solvothermalen Verfahren aus nachhaltigem Furfural, welches über Lignocellulose erhältlich ist, hergestellt. Aldehydgruppen der Oberfläche reagierten mit Hydroxylamin zu dem entsprechendem Oxim, während die Reaktion mit Benzoylchlorid zu einem bio‐basierten Typ I Photoinitiator (CD‐PI) führte, welcher nachhaltige Kohlenstoffpunkte enthält. Die Fähigkeit zur Photoinitiierung wurde unter UV‐Bestrahlung bei 365 nm mit dem traditionellen Photoinitiator (PI) Ethyl (2,4,6‐trimethyl benzoyl) phenyl phosphinat (TPO‐L) mittels Echtteit FTIR Spektroskopie verglichen. Die auf einem Gemisch von Urethandimethacrylat (UDMA) und Tripropylenglykoldiacrylat (TPGDA) basierte Photopolymerzusammensetzung führte unter Verwendung von CD‐PI oder TPO‐L zu einem ähnlichen Endumsatz von etwa 70 %. Dennoch erschien das vernetzte Material im Fall der Zusammensetzungen, die mit CD‐PI verarbeitet wurden, homogen, während jene, die mit TPO‐L hergestellt wurden, heterogen waren, was durch die beiden Glasübergangstemperaturen gezeigt wurde. Außerdem war die Migrationsgeschwindigkeit von CD‐PI in den gehärteten Proben geringer im Vergleich zu jenen Proben für die TPO‐L als PI eingesetzt wurde.

Type I Photoinitiator Based on Sustainable Carbon Dots.

Sustainable carbon dots comprising surficial oxime ester groups following homolytic bond cleavage exhibit potential as photoinitiators for traditional free radical photopolymerization. Carbon dots were made following a solvothermal procedure from sustainable furfural available from lignocellulose. Surficial aldehyde moieties reacted with hydroxylamine to the respective oxime while reaction with benzoyl chloride resulted in a biobased Type I photoinitiator comprising sustainable carbon dot (CD-PI). Photoinitiating ability was compared with the traditional photoinitiator (PI) ethyl (2,4,6-trimethyl benzoyl) phenyl phosphinate (TPO-L) by real-time FTIR with UV exposure at 365 nm. Photopolymer composition based on a mixture of urethane dimethacrylate (UDMA) and tripropylene glycol diacrylate (TPGDA) resulted in a similar final conversion of about 70 % using either CD-PI or TPO-L. Nevertheless, it appeared homogeneous in the case of compositions processed with CD-PI, while those made with TPO-L were heterogeneous as shown by two glass transition temperatures. Moreover, the migration rate of CD-PI in the cured samples was lower in comparison with those samples using TPO-L as PI.

Post-processing of a 3D-printed denture base polymer: Impact of a centrifugation method on the surface characteristics, flexural properties, and cytotoxicity

ObjectivesTo investigate the impact of a centrifugation method on the surface characteristics, flexural properties, and cytotoxicity of an additively manufactured denture base polymer. MethodsThe tested specimens were prepared by digital light processing (DLP). A centrifugation method (CENT) was used to remove the residual uncured resin. In addition, the specimens were post-processed with different post-rinsing solutions: isopropanol (IPA), ethanol (EtOH), and tripropylene glycol monomethyl ether (TPM), respectively. A commercial heat-polymerized polymethyl methacrylate was used as a reference (REF). First, the values of surface topography, arithmetical mean height (Sa), and root mean square height (Sq) were measured. Next, flexural strength (FS) and modulus were evaluated. Finally, cytotoxicity was assessed using an extract test. The data were statistically analyzed using a one-way analysis of variance, followed by Tukey's multiple comparison test for post-hoc analysis. ResultsThe Sa value in the CENT group was lower than in the IPA, EtOH, TPM, and REF groups (p < 0.001). Moreover, the CENT group had lower Sq values than other groups (p < 0.001). The centrifugation method showed a higher FS value (80.92 ± 8.65 MPa) than the EtOH (61.71 ± 12.25 MPa, p < 0.001) and TPM (67.01 ± 9.751 MPa, p = 0.027), while affecting IPA (72.26 ± 8.80 MPa, p = 0.268) and REF (71.39 ± 10.44 MPa, p = 0.231). Also, the centrifugation method showed no evident cytotoxic effects. ConclusionsThe surfaces treated with a centrifugation method were relatively smooth. Simultaneously, the flexural strength of denture base polymers was enhanced through centrifugation. Finally, no evident cytotoxic effects could be observed from different post-processing procedures. Clinical significanceThe centrifugation method could optimize surface quality and flexural strength of DLP-printed denture base polymers without compromising cytocompatibility, offering an alternative to conventional rinsing post-processing.

Effect of radiation sensitizer on the friction, mechanical and thermal degradation properties of electron beam cured FKM-PTFE composite

Friction coefficient behaviour of electron beam cured vinylidene fluoride-hexafluoropropylene copolymer fluorocarbon rubber (FKM) with 30% loading of polytetrafluoroethylene micro-powder (PTFEMP) irradiated at 250 kGy dose were studied by using a pin-on-disk tribometer for a total testing distance of 360 m in dry conditions at a sliding speed and applied normal load (FN) of 0.05 m/s and 1 N respectively. The same tests were done on the 70/30 blend added with radiation sensitizers n,n-1,3 phenylene bismaleimide (HVA2), trimethylol propane triacrylate (TMPTA) and tripropylene glycol diacrylate (TPGDA). The average friction coefficient (μ) value of all the composites with sensitizer decreased with the TMPTA system recording the lowest μ value which reduced by almost half compared to the pure composite due to better crosslinking density of the vulcanizate. Analysis of the friction coefficient curve behaviour showed an initial low value but displaying an increasing trend versus distance in the TMPTA and TPGDA composites while HVA2 composite recorded an initial high value but showed a reducing trend versus distance. HVA2 composite also recorded the best tensile strength results due to its influence in promoting better synergistic effect and miscibility of PTFEMP filler in FKM matrix.

Photobleachable coumarin-thioester derivatives with low cytotoxicity as visible-light photoinitiators for free radical and cationic photopolymerization

The development of photoinitiators is suffering from deep color, low solubility, and biotoxicity caused by the introduction of large-conjugated structures, also the complex synthetic procedures constrain the application of photoinitiators. To overcome this issue, nine kinds of coumarin thioester photoinitiators (CTEs) have been delicately designed and synthesized through a simple, metal-free two-step reaction. CTEs with excellent light absorption properties in the visible light range can be used not only as a type I photoinitiator but also as a type II photoinitiator, and sensitizer in the cationic photoinitiating system. CTEs effectively initiate the photopolymerization of tripropylene glycol diacrylate (TPGDA) under the irradiation of 405 nm LED, and the double bond conversions are similar to or better than those of commercial photoinitiators. Also, the cationic photopolymerization of bisphenol A diglycidyl ether (BADGE) is successfully initiated by CTEs/IOD systems. Notably, the epoxy group conversion initiated by 6O-CTE/IOD reaches 72.1 %, surpassing that of the commercial photoinitiating system. The photoinitiating mechanism of CTEs is proposed and supported by theoretical calculations. Furthermore, the bond cleavage abilities of CS bonds endow CTEs with photobleaching properties. The colorless cured film initiated by 6O-CTE was obtained under only 15 s irradiation, indicating their application prospects of CTEs in colorless photopolymerization. More importantly, the cytotoxicity of CTEs is much lower than that of commercial photoinitiator TPO. This work provides new insight into the design of biocompatible photoinitiators with a photobleaching property for LED photopolymerization.

Simultaneous quantification of seven glycols in antifreeze liquids using direct liquid injection gas chromatography coupled with mass spectrometry

Glycol‐based antifreeze liquids, commonly composed of ethylene glycol or propylene glycol, have important uses in automotive cooling, but they should be handled with care due to their toxicity. Ethylene glycol is highly toxic to humans and animals. A fast, accurate, precise, and robust method was developed for the simultaneous quantification of seven most important glycols and their isomers.MethodsGlycols were analyzed from diluted sample solution of coolants using gas chromatography coupled with mass spectrometry (GC–MC) in single ion monitoring mode.ResultsThe method was developed and validated for seven individual glycols (ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, propylene glycol, dipropylene glycol, and tripropylene glycol). Limits of detection (1–2 μg/mL) and limits of quantification (10 μg/mL) obtained were appropriate. The present method was applied for the determination of glycols in 10 different antifreeze liquids commercially available on the Romanian market, proving to be reliable.ConclusionsA method that requires only a two‐step dilution of antifreeze samples combined with direct liquid injection GC–MS was validated for the simultaneous quantification of seven glycols (and their isomers) in 10 different types of antifreeze liquids. The results obtained in the validation procedure proved that the GC–MS method is sensitive and precise for the quantification of glycols.

3D-printable hydrophobic silicone inks for antiadhesion tough objects via molecular engineering

3D printable hydrophobic ink is highly desirable to simply print hydrophobic objects for various applications, such as oil/water separation. However, printable hydrophobic monomers/inks are limited which seriously restricts the fabrication and application of 3D printing hydrophobic objects. Herein, simulating the crown, trunk, and roots of trees from the molecular levels, coatings/objects were designed and prepared using a 6-functional hyperbranching polyurethane acrylate (PUA) monomer as the “trunk”, mono-acrylate terminated polydimethylsiloxane (Vi-PDMS) as the “leaf”, and tripropylene glycol diacrylate (TPGDA) as the “root”. The printed objects with excellent mechanical properties and stable hydrophobicity with CAs and SAs in the range of 80°–110° and 10°–30°, respectively, and could be used in a variety of environments (e.g., acid-based solution, seawater) for a month. Cylindrical, ladder, and mushroom-shaped micro-nano structures could be prepared to improve the hydrophobicity of the printed objects to achieve CAs up to ∼170°. The antiadhesion tough teeth and microchannels could be prepared facilely with the hydrophobic inks. This work demonstrates a simple and rapid method to manufacture various complex and sophisticated hydrophobic coatings/objects and a broader strategy for 3D printing technology.

Photo-assisted ultrasonic curing for ultrafast and deep prototyping based on coumarin derivatives

Although photocuring is currently the most commonly used method in 3D additive manufacturing, it still faces significant challenges in rapid prototyping of thick materials due to the limited penetration of light. Ultrasonic technology has the advantages of high penetration depth and unparalleled cavitation, offering opportunities for enabling additive manufacturing of thick materials. In this study, a coumarin-based two-component system composed of Coum-Ph-OC12H25 and N-phenylglycine as initiator and hydrogen supplier, respectively, was developed to achieve ultrasonic curing of tripropylene glycol diacrylate (TPGDA). The ideal curing efficiency of this two-component system was optimized to 90 %, and ultrasonic curing of thick materials was achieved with a penetration depth of up to 15 cm. Moreover, electron spin resonance (ESR) spectroscopic measurements demonstrated the free-radical reaction mechanism. It is believed that this research has the potential to expand the 3D additive manufacturing technology and pave the way for future developments in this field.

Enhancing the sound and thermal insulation properties of polypropylene foam by preparing high melt strength polypropylene.

High-performance polypropylene (PP) foam is a vital polymer product in industrial areas. However, the poor melt strength of ordinary PP homopolymer limits its foaming molding. In this work, high melt strength polypropylene (HMSPP) was prepared by using styrene (St) and tripropylene glycol diacrylate (TPGDA) as comonomers, and then PP foams were prepared by mold foaming method. The results showed that adding St in the grafting process of TPGDA will obviously improve the melt strength of the PP matrix, and its melt strength (28184Pa.s) is 7.4 times higher than that of pure PP. HMSPP foam has more regular and uniform cells and higher cell density, which significantly improves the sound and thermal insulation properties of PP foam. Compared with pure PP foam, the average sound transmission loss (52.9dB) of HMSPP foam with a low foaming ratio increased by 64%, and the thermal conductivity (0.0867W/mK) decreased by 46%. Therefore, the obtained HMSPP foam can be used in sound insulation or thermal insulation area. This work provides an available route for the high-performance utilization of PP foam. This article is protected by copyright. All rights reserved.

A Dual‐Functional Organic Electrolyte Additive with Regulating Suitable Overpotential for Building Highly Reversible Aqueous Zinc Ion Batteries

AbstractAqueous zinc ion batteries (AZIBs) with high safety, low cost, and eco‐friendliness advantages show great potential in large‐scale energy storage systems. However, their practical application is hindered by low Columbic efficiency and unstable zinc anode resulting from the side reactions and deterioration of zinc dendrites. Herein, tripropylene glycol (TG) is chosen as a dual‐functional organic electrolyte additive to improve the reversibility of AZIBs significantly. Importantly, ab initio molecular dynamics theoretical simulations and experiments such as in situ electrochemical impedance spectroscopy, and synchrotron radiation‐based in situ Fourier transform infrared spectroscopy confirm that TG participates in the solvation sheath of Zn2+, regulating overpotential and inhibiting side reactions; meanwhile, TG inhibits the deterioration of dendrites and modifies the direction of zinc deposition by constructing an adsorbed layer on the zinc anode. Consequently, a Zn‐MnO2 full cell with TG electrolyte exhibited a specific capacity of 124.48 mAh g‐1 after 1000 cycles at a current density of 4 A g‐1. This quantitative regulation for suitable solvation sheath and adsorbed layer on zinc anode, and its easy scalability of the process can be of immediate benefit for the dendrite‐free, high‐performance, and low‐cost energy storage systems.

Study on The Emulsion Stability of Tripropylene Glycol Diacrylate in Water

Study on The Emulsion Stability of Tripropylene Glycol Diacrylate in Water

A quantum chemical computation and model investigation for autoignition kinetic of a long chain oxygenate: Tri-propylene glycol methyl ether

Tri-propylene glycol methyl ether (TPGME) is a promising bio-based oxygenated fuel for advanced engines. The internal H-migration of peroxy (ROO) radicals is a critical factor in the process of TPGME autoignition. In this work, the potential energy surfaces (PESs) of the internal H-migration of ROO radicals as well as alcohol elimination of TPGME were calculated with a high-level DLPNO-CCSD(T)/cc-pVTZ//B3LYP-D3/6–311++G(d,p) method. Rate constants for target reactions were then obtained over a temperature range of 300–1000 K using conventional transition state (CTST) theory. The rate constants for above reactions in the Burke’s model [Combust. Flame. 2015, 16 2(7), 2916–2927] were updated with the calculated results, followed by the modification for important reaction using an analogy strategy, to obtain a revised model. It was found that the feasibility of the H-migration of ROO radicals depended on the transition state ring size and the C-H bond energy of the transferred hydrogen atom, with 1, 5H-migration and 1, 6H-migration played a leading role in the process of TPGME autoignition. Validation against the shock tube (ST), jet stirred reactor (JSR) and collaborative fuel research (CFR) engine measurements from the literature showed that the revised model improved the prediction accuracy. In comparison to n-heptane, the CFR simulation proved that more available hydrogens of 1,5H-migration and 1,6H-migration, as well as higher concentrations and rate of production (ROP) for key low-temperature intermediate species, were contributing factors that stronger low-temperature oxidation activity of TPGME.

A surrogate modelling strategy to improve the surface morphology quality of inkjet printing applications

Current trends in manufacturing electronics feature digital inkjet printing as a key technology to enable the production of customised and microscale functional devices. However, electrical device performance depends on the accuracy and uniformity of the printed-track morphology, which presents significant quality challenges in current applications. Several studies to predict the morphology of printed features have been developed using computationally expensive physics-based simulations, but little attention has been paid to reduced order models suitable for fast production conditions. Here we propose a surrogate modelling framework to improve the inkjet-printed track morphology created by the sequential deposition of microdroplets on non-porous substrates. Assuming physical properties of a UV-curable dielectric ink made from tripropylene glycol diacrylate (TPGDA), a set of response surface equations built from a validated lattice Boltzmann simulation predict the track morphology as a function of drop spacing and contact angle hysteresis with an error percentage less than 10 %. Furthermore, the surrogate model is able to capture transient effects observed in experiments and builds track morphology in seconds, enabling efficient optimisation of printing and wetting parameters. The simplicity of the proposed technique makes it a promising tool for model driven inkjet printing process optimization, including real time process control and paves the way for better quality devices in the printed electronics industry.

Sugar-Core Synthesized Multibranched Polylactic Acid and Its Diacrylate Blends as a UV LED-Curable Coating with Enhanced Toughness and Performance

Exploring the application of biodegradable/bioplastic coating material for eco-friendly and sustainable packaging is one of the global challenges being tackled. In this context, we propose (i) the synthesis of multibranched polylactic acid (PLA) using table sugar mainly composed of sucrose as a core initiator, and (ii) a model formula for sugar-based PLA (suPLA) and its diacrylate blends as a UV LED-curable coating. The synthesis of suPLA through ring-opening polymerization (ROP) was optimized by sugar: l-lactide (L-LA) molar ratio, temperature, and reaction time. suPLA, with a Mw of ∼1000 g/mol, was obtained with a maximum yield of around 80%. To establish a model UV LED-curable bioplastic-based coating, the suPLA with different content was formulated in tripropylene glycol diacrylate (TPGDA) as a diluent monomer. The influence of curing time (0–60 s) on double bond conversion for turning the liquid coating to a solid film of the suPLA/TPGDA blending system was assessed. Aiming to validate the influence of the curing degree, changes in the chemical function, thermal stability, glass transition temperature, crystallization temperature, and enthalpy were also characterized. By increasing the suPLA content, the tensile tests on the UV LED-cured suPLA-TPGDA films showed significant improvement in terms of toughness. The coating surface morphologies and optical properties (i.e., gloss value, color difference, yellowness, and whiteness indexes) were also determined. It is worth noting that the sugar molecule and multibranched structure play an important role in moisture absorption. The biodegradation test demonstrated that the UV LED-cured suPLA-TPGDA film exhibited biodegradation phenomena, as analyzed from CO2 production, physical appearance, changes of mass, chemical functions, and thermal stability. The current study showed that the suPLA and its diacrylate blends are promising biobased, printable, and UV LED-curable coating prototypes to create a tough film for a sustainable packaging approach in the future.

UV curing behavior of a liquid polyborosilazane and stereolithography to SiBCN ceramic components

The ultraviolet (UV) curing behavior and kinetics both in air and in nitrogen atmosphere of a liquid polyborosilazane were investigated by differential scanning photo calorimeter (DPC) measurement and real-time FTIR techniques. The results showed that the bifunctional acrylic reactive diluent tripropylene glycol diacrylate (TPGDA) content, photo-initiator concentration, and temperature had their optimal values to get the maximum ultimate reaction rate and conversion percentage. It's noteworthy that the addition of TPGDA will greatly enhance polymerization rate and conversion percentage within a very short time-frame. While the rate in air is higher than in nitrogen atmosphere, probably owing to the effect of oxidation curing, which is coordinated with the calculation results of activation energy.Based on the above experiment, we also report on the direct fabrication of SiBCN ceramic components from preceramic polyborosilazanes by stereolithography and subsequent pyrolysis at 900 ○C for 4 h. The TGA curve shows the ceramic yield is 51.1% after pyrolysis at 1200 ○C. A linear shrinkage of 27%, associated with the polymer-to-ceramic conversion, was observable and the density of pyrolyzed SiBCN is about 2 g cm−3 with slight residual porosity. The indentation hardness is 9.83 GPa and the modulus is 77.1 GPa after heat-treatment at 1400 ○C for 3 h.

Influence of postwashing process on the elution of residual monomers, degree of conversion, and mechanical properties of a 3D printed crown and bridge materials.

This study aimed to determine the effects of the postwashing method and time on the mechanical properties and biocompatibility of three-dimensional (3D) printed crown and bridge resin. DLP (digital light processing)-printed specimens produced from Nextdent crown & bridge (C&B) resins were washed separately using an ultrasonic bath and rotary washer with TPM (tripropylene glycol monomethyl ether) for 3min, 6min, 10min, 20min, and 1h. Postcuring was applied for 30min to each specimen after the washing process. The flexural strength, Vickers hardness, water sorption and solubility, degree of conversion (DC), elution of residual monomers, and biocompatibility of the specimens were evaluated. The ultrasonic bath showed greater washing efficacy by reducing the residual HEMA (2-hydroxyethyl methacrylate) from 2.0634ppm to 0.1456ppm and reducing the residual TEGDMA (triethylene glycol dimethacrylate) from 1.4862ppm to 0.1484ppm. With prolonged washing, the flexural strength significantly decreased from 129.67±6.66MPa (mean±standard deviation) to 103.17±7.20MPa, while the Vickers hardness increased slightly for the first 6min and then decreased thereafter significantly. The DC was 87.78±1.34% after 3min and then gradually decreased with extended washing time. The cytotoxicity significantly decreases with the increment of the washing time. The washing effect on the elution of residual monomers was better for an ultrasonic bath than for a rotary washer. Extending the washing time reduces the mechanical properties and cytotoxicity of the Nextdent C&B resin.

THE EFFECT OF THE ACRYLATE MONOMER ON THE CHARACTERISTICS OF PHOTOPOLYMERIZABLE SUSPENSIONS FOR THE PRODUCTION OF CERAMICS FROM STABILIZED ZrO2

The influence of the structure and properties of acrylate monomers on the rheology and polymerization of suspensions containing partially stabilized zirconium dioxide, a dispersant and a photoinitiator as a ceramic filler is investigated. It has been shown that the use of the DISPERBYK 2013 additive makes it possible to obtain suspensions containing 1,6-hexanediol diacrylate, dipropylene glycol diacrylate and tripropylene glycol diacrylate with a viscosity value below 5 Pa?s at high (up to 41 vol. %) filling with TZ-3YS-E powder. The possibility of using the obtained suspensions for three-dimensional printing of high-density ceramic products with complex geometry has been established.

Ultrasonic study of the elastic properties of propylene glycol oligomers in the glassy state and during the glass–liquid transition

ABSTRACT Using an ultrasonic technique under pressure, we investigated the dependence of elastic properties of propylene glycol, dipropylene glycol and tripropylene glycol on the concentration of hydrogen bonds and the mass of molecules. Studies were carried out up to 1.8 GPa in the glassy state and at isobaric heating during the glass–liquid transition. Propylene glycol in glassy state has the highest modules, and its interaction potential is more central than in di- and tripropylene glycol. Both the shear modulus G and the bulk modulus B are practically identical for glassy di- and tripropylene glycol.