Poly Propylene Oxide Research Articles

Enhanced Flotation Separation of Iron and Silicon with Branched Block Polyethylene Oxide Polypropylene Oxide and Sodium Oleate: Mechanisms and Flotation Behavior

This study explores the strengthening mechanism of the surfactant branched block polyethylene oxide–polypropylene oxide (BB-PEO-PPO) in sodium oleate (NaOL) flotation systems. A comprehensive characterization of BB-PEO-PPO was performed using flotation experiments, contact angle measurements, surface tension analysis, zeta potential measurements, infrared spectroscopy, and foam dynamics assessments. Flotation results showed that the combination of BB-PEO-PPO and NaOL improved iron recovery by 2.71% and reduced the total iron (TFe) grade in tailings by 2.05%, demonstrating a significant enhancement in collecting efficiency. The addition of BB-PEO-PPO effectively reduced foam size and lowered the zeta potential on the surface of activated quartz. At a slurry temperature of 15 °C, BB-PEO-PPO increased the solubility of NaOL radicals, facilitating their chemical adsorption onto activated quartz and improving the hydrophobicity of quartz particles. Notably, the presence of BB-PEO-PPO extended the flotation foam discharge time (D50) by 50% without substantially increasing foam volume, thereby significantly enhancing foam stability.

On the Complex Flow Dynamics of Shear Thickening Fluids Entry Flows

Due to their nature, using shear thickening fluids (STFs) in engineering applications has sparked an interest in developing energy-dissipating systems, such as damping devices or shock absorbers. The Rheinforce technology allows the design of customized energy dissipative composites by embedding microfluidic channels filled with STFs in a scaffold material. One of the reasons for using microfluidic channels is that their shape can be numerically optimized to control pressure drop (also known as rectifiers); thus, by controlling the pressure drop, it is possible to control the energy dissipated by the viscous effect. Upon impact, the fluid is forced to flow through the microchannel, experiencing the typical entry flow until it reaches the fully developed flow. It is well-known for Newtonian fluid that the entrance flow is responsible for a non-negligible percentage of the total pressure drop in the fluid; therefore, an analysis of the fluid flow at the entry region for STFs is of paramount importance for an accurate design of the Rheinforce composites. This analysis has been numerically performed before for shear-thickening fluids modeled by a power-law model; however, as this constitutive model represents a continuously growing viscosity between end-viscosity plateau values, it is not representative of the characteristic viscosity curve of shear-thickening fluids, which typically exhibit a three-region shape (thinning-thickening-thinning). For the first time, the influence of these three regions on the entry flow on an axisymmetric pipe is analyzed. Two-dimensional numerical simulations have been performed for four STFs consisting of four dispersions of fumed silica nanoparticles in polypropylene glycol varying concentrations (7.5–20 wt%).

Investigation on the thermal, mechanical, and antibacterial properties of polymer nanocomposites from waste polypropylene and cerium oxide nanoparticles

Investigation on the thermal, mechanical, and antibacterial properties of polymer nanocomposites from waste polypropylene and cerium oxide nanoparticles

Dilational rheological properties of extended anionic surfactants at decane-water interface

The dynamic interfacial dilational properties of extended surfactants octadecyl-(polypropylene oxide)m-(polyethylene oxide)n-carboxylic sodium (C18POmEOnC) with different numbers of polypropylene oxide (PO) and polyethylene oxide (EO) groups at the decane–water interface were investigated by means of oscillating drop method. The influences of interface ageing time, dilational frequency, bulk concentration and interfacial pressure on the dilational properties were investigated. The experimental results demonstrate that, at low concentrations, the adsorption film is predominantly influenced by diffusion exchange, while intermolecular interactions at the interface play a more significant role at high concentrations. Beyond the critical micelle concentration (CMC), the primary relaxation process in the adsorption film is driven by the formation of micellar structures. Additionally, the weak hydrophobic PO groups exhibit compressibility and extensibility, facilitating the formation of spring-like helical structures at the decane–water interface. As a result, the dilational modulus increases and the phase angle decreases in low concentration with the increase of PO number. With increasing concentration, the weak hydrophilic EO chains gradually transition from a partially flat state to an upright orientation toward the aqueous phase, forming sublayer structures through polar interactions. At this stage, the increase in EO group chain length has a more pronounced impact on the elastic modulus compared to PO groups. These experimental findings suggest the existence of a mechanistic model for the extended surfactant adsorption films.

Phytochemical Analysis and In Vitro Effects on Isolated Murine Lymphocytes and Macrophages of Polymeric Micelles Loaded with Cycloartane Saponin

Triterpenoid saponins from the Astragalus species possess valuable effects (cytotoxic, adjuvant, hepatoprotective, neuroprotective, antiviral, etc.). Some also have immunomodulatory activities. Astragalus glycyphyllos is distributed in Bulgaria and mainly accumulates cycloartane saponins. From the overground parts of the species, a triterpenoid cyloartane-type saponin (AGOS3) was isolated by different chromatographic techniques. A quantitative LC-MS method for the determination of the saponin was developed and validated. Further, the saponin was loaded in copolymeric micelles based on triblock copolymers of polyethylene oxide and polypropylene oxide (Pluronics). The LC-MS method was applied on the developed micelles to determine their loading degrees. Afterwards, the possible pharmacological effects of free and encapsulated in polymeric nanoparticles of triterpenoid saponin (1, 5, 10, 25, 50, and 100 µg/mL) were evaluated in isolated murine macrophages and lymphocytes in vitro. Free AGOS3 stimulated proliferation only at the highest tested concentrations (50–100 µg/mL), and the effect was more evident in isolated macrophages. Interestingly, AGOS3-loaded polymeric micelles caused concentration dependency and statistically significant increases in the proliferation of both isolated lymphocytes and macrophages, even at a lower concentration (10 µg/mL). These results could serve as the basis for further research on the immunomodulatory effect of this saponin.

Synthesis and Investigation of Catalytic Properties of Metal-Polymer Nanocomposites Based on Unsaturated Polyester Resins

This paper focuses on the hydrogenation process in metal-polymer complexes based on copolymers of polypropylene glycol fumarate phthalate and polypropylene glycol maleate phthalate, using acrylic acid and immobilized cobalt metal particles as catalysts. A classical reaction of the electrocatalytic hydrogenation of pyridine to piperidine was applied. SEM and dynamic light scattering were utilized to investigate the average size and dispersity of cobalt metal nanoparticles. The experimental findings show that the efficiency of hydrogenation can be improved by increasing the temperature from 25 to 40 °C and the current to 2 A. More specifically, increasing the temperature to 40 °C promotes swelling of the polymer and its transition from a globular collapsed state to an open one, which leads to an increase in the number of active catalytic centers and, as a consequence, acceleration of the hydrogenation process. Increasing the current strength to 2 A also helps to increase the rate of the hydrogenation process. Further increasing the current to 3 A is undesirable due to an increase in the yield of by-products and a decrease in the yield of the target product, piperidine. Based on a comparative analysis, it was established that the use of a copolymer of polypropylene glycol maleate phthalate with acrylic acid as the polymer matrix base is the most preferable for obtaining polymer-metal complexes with nanosized cobalt.

Stochastic dynamics mass spectrometric and Fourier transform infrared spectroscopic structural analyses of composite biodegradable plastics

<p>The (partial) replacement of synthetic polymers with bioplastics is due to increased production of conventional packaging plastics causing for severe environmental pollution with plastics waste. The bioplastics, however, represent complex mixtures of known and unknown (bio)polymers, fillers, plasticizers, stabilizers, flame retardant, pigments, antioxidants, hydrophobic polymers such as poly(lactic acid), polyethylene, polyesters, glycol, or poly(butylene succinate), and little is known of their chemical safety for both the environment and the human health. Polymerization reactions of bioplastics can produce no intentionally added chemicals to the bulk material, which could be toxic, as well. When polymers are used to food packing, then the latter chemicals could also migrate from the polymer to food. This fact compromises the safety for consumers, as well. The scarce data on chemical safety of bioplastics makes a gap in knowledge of their toxicity to humans and environment. Thus, development of exact analytical protocols for determining chemicals of bioplastics in environmental and food samples as well as packing polymers can only provide warrant for reliable conclusive evidence of their safety for both the human health and the environment. The task is compulsory according to legislation Directives valid to environmental protection, food control, and assessment of the risk to human health. The quantitative and structural determination of analytes is primary research task of analysis of polymers. The methods of mass spectrometry are fruitfully used for these purposes. Methodological development of exact analytical mass spectrometric tools for reliable structural analysis of bioplastics only guarantees their safety, efficacy, and quality to both humans and environment. This study, first, highlights innovative stochastic dynamics equations processing exactly mass spectrometric measurands and, thus, producing exact analyte quantification and 3D molecular and electronic structural analyses. There are determined synthetic polymers such as poly(ethylenglycol), poly(propylene glycol), and polyisoprene as well as biopolymers in bags for foodstuffs made from renewable cellulose and starch, and containing, in total within the 20,416–17,495 chemicals per sample of the composite biopolymers. Advantages of complementary employment in mass spectrometric methods and Fourier transform infrared spectroscopy is highlighted. The study utilizes ultra-high resolution electrospray ionization mass spectrometric and Fourier transform infrared spectroscopic data on biodegradable plastics bags for foodstuffs; high accuracy quantum chemical static methods, molecular dynamics; and chemometrics. There is achieved method performance |<em>r</em>| = 0.99981 determining poly(propylene glycol) in bag for foodstuff containing 20,416 species and using stochastic dynamics mass spectrometric formulas. The results highlight their great capability and applicability to the analytical science as well as relevance to both the fundamental research and to the industry.</p>

Integrative process of extraction and purification of tagitinin C using ethanolic two-phase system based on protic ionic liquids

Tithonia diversifolia is a tropical plant composed of several compounds with medicinal properties. This study aimed to design a sequential process for the extraction of tagitinin C from T. diversifolia using organic solvents (acetone, acetonitrile, methanol, and ethanol) and purification in the ethanolic two-phase system (ETPS) formed by protic ionic liquids (PILs), polypropylene glycol 2000 (PPG-2000) and ethanol, reported here for the first time. The extraction process variables such as type of solvent, solid–liquid ratio, temperature, and process time were evaluated. Ethanol was the best tagitinin C extracting agent (702.1 µg/mL). Phase diagrams were constructed using PPG-2000, PIL, and ethanol at 298.15 K. The sequencing with the purification process occurred by adding the other constituents directly into the ethanol extract. Tagitinin C preferentially migrated to the top phase (rich in PPG-2000), while phenolic compounds (contaminants) were partitioned mainly to the opposite phase (PIL-rich phase). ETPS formed by [2HEA][Ac] (15.52 wt%) + PPG 2000 (49.91 wt%) + ethanol (34.57 wt%) at 298.15 K presented the highest selectivity (S = 18.3), extraction efficiency in the top phase (EE% = 86 %) and purification factor (3.4-fold), demonstrating the ability of ETPS to selectively and sequentially extract and purify tagitinin C.

Self-Healable, Transparent, Biodegradable, and Shape Memorable Polyurethanes Derived from Carbon Dioxide-Based Diols.

A series of CO2-based thermoplastic polyurethanes (TPUs) were prepared using CO2-based poly(polycarbonate) diol (PPCDL), 4,4'-methylenebis (cyclohexyl isocyanate) (HMDI), and polypropylene glycol (PPG and 1,4-butanediol (BDO) as the raw materials. The mechanical, thermal, optical, and barrier properties shape memory behaviors, while biocompatibility and degradation behaviors of the CO2-based TPUs are also systematically investigated. All the synthesized TPUs are highly transparent amorphous polymers, with one glass transition temperature at ~15-45 °C varying with hard segment content and soft segment composition. When PPG is incorporated into the soft segments, the resultant TPUs exhibit excellent self-healing and shape memory performances with the average shape fixity ratio and shape recovery ratio as high as 98.9% and 88.3%, respectively. Furthermore, the CO2-based TPUs also show superior water vapor permeability resistance, good biocompatibility, and good biodegradation properties, demonstrating their pretty competitive potential in the polyurethane industry applications.

Blends of polydimethylsiloxane-based polyurethane and poly (propylene glycol)-based polyurethane with co-continuous structures: Morphology evolution, synergistic effects and application in strain sensors

Blending is an effective way to improve properties of rubbers and develop new materials, so more than 75 % of the rubber consumption in the world is rubber blend. However, blending of thermoplastic elastomers has not yet been emphasized, and few successful examples have been reported. The main challenge for blend systems is compatibility of two components. Herein, a series of (polydimethylsiloxane-based PU)-g-(poly (propylene glycol)-based PU) ((PDMS-PU)-g-(PPG-PU)) graft copolymers with different graft chain lengths and hard segment contents (HSC) were synthesized and utilized as compatibilizers of PDMS-PU/PPG-PU blends. The influence of the structure of compatibilizers on the morphology of blends was investigated, and the compatibilization mechanism was proposed. With the solubilization, the phase structure of blends transforms from “droplet-in-matrix” morphologies to co-continuous ones, and the average size of PPG-PU dispersed phase decreases from 3.5 ± 0.45 μm to 230 ± 60 nm. This is the first time that thermoplastic PDMS-PU/PPG-PU blends with co-continuous structures have been successfully prepared. The properties of blends exhibit synergistic effects. For example, they show high tensile strength of PPG-PU in mechanical properties and unique properties of PDMS in dynamic mechanical properties, weather resistance, water resistance and biocompatibility. In addition, strain sensors were fabricated by introducing carbon nanotubes (CNTs) into the blends, which demonstrated remarkable sensing capability for diverse human body motions.

Components optimization of polyurethane-modified asphalt binder towards compatibility: Insight from molecular dynamics simulations

Polyurethane-modified asphalt demonstrated the enhanced durability and skid resistance, while remaining the drawback in the compatibility between the polyurethane modifier and asphalt binder in practical use. Herein, a molecular-dynamics-simulations based compatibility evaluation method is proposed for the polyurethane modifier and asphalt binder, thereby achieving the cost-effective and efficient components optimization. Twelve components asphalt molecular model was built in Molecular Dynamics to investigate the interaction of asphalt binder to the polypropylene glycol, toluene diisocyanate, and diphenylmethane diisocyanate, respectively. The molecular model of polyurethane modified asphalt binder was verified by the similar loss modulus temperature from the simulation and temperature scanning tests. The simulation outcomes indicate significant variations in the compatibility of different polyurethanes with asphalt, in which diphenylmethane diisocyanate-type polyurethane exhibits the superior compatibility. The compatibility of various polyurethane concentrations in asphalt shows considerable disparity, suggesting that the compatibility index can serve as a criterion for determining the optimal dosage of the modifier. Temperature also exerts an influence on the compatibility of polyurethane modified asphalt binder. Simulation results indicates that 130 °C potentially may be the optimal temperature for its preparation, which is corroborated by the microscopic characterization. This study provides a fundamental framework for the molecular dynamics simulation-based components optimization of polyurethane-modified asphalt, thereby inspiring the targeted design of asphalt materials.

Concentrations and carbonyl index of microplastic in surface seawater in southeastern coastal region off Japan, Northwestern Pacific

In this study, microplastic concentrations in the southeastern coastal regions of Japan were measured along the northward ocean current at seven stations from Okinawa to Tokai region. Concentrations ranged from 0.014 to 0.094 pieces/m3, except for a station near the Bungo Channel mouth, which had 0.723 pieces/m3. Polystyrene (PS) foam was most prevalent near the east side of Kyushu, suggesting origination from nearby coastal areas. Fragmentation levels were higher in the Tokai region. In addition, carbonyl index (CI) of polyethylene (PE) microplastics increased northward, indicating northward movement from southern regions. Standard PE microplastics showed chemical treatment does not significantly alter CI values. Further spectral analysis suggested potential oxidation of polypropylene (PP) and PS foam by chemical treatment. This study provides a comprehensive understanding of the abundance, distribution, and characteristics of microplastics in the southeastern coastal regions of Japan in the northwest Pacific, enhancing the understanding of environmental fate of microplastics.

A facile strategy for synthesizing isosorbide-based polyurethane structural adhesives and core–shell rubber

A structural adhesive series of biomass-based polyurethane (Biomass-PU) is synthesized using polypropylene glycol (PPG2000), isosorbide-based polyol (RPO300) as polyols, isophorone diisocyanate (IPDI) as an isocyanate and 4-tert-butylphenol (BP) as a capping agent. Three different equivalent ratios of PPG2000/RPO300, 9/1 (Biomass-PU1), 7/3 (Biomass-PU2), and 1/1 (Biomass-PU3), are evaluated to determine the effect of isosorbide-based polyol content on the properties and the optimizing formulation of biomass-PU structure adhesive. The 9/1 ratio of PPG2000/RPO300 substantially leads to the improvement of impact strength by up to 35 MPa, and the PPG2000/RPO300 = 9/1 ratio exhibits better thermal properties and impact strength than those of other ratios. To achieve more compatibility between biomass-PU structure adhesive and core–shell rubber (CSR) toughener, novel CSRs are successfully synthesized using acryl-PU as a shell and biomass-based PU as a core. The chemical structure of biomass-PU structure adhesives is analyzed through FT-IR Spectroscopy and NCO% titration. Thermal properties are evaluated using TGA and DSC analysis. Their molecular weights are measured by GPC. Also, the core–shell rubber (CSR) with a polyurethane shell is prepared to reinforce the impact strength of Biomass-PU structure adhesive.

Optically clear pressure‐sensitive adhesive with flexible crosslinking agent for high recovery efficiency, low energy storage modulus, and excellent folding resistance

AbstractOptically clear pressure‐sensitive adhesive (OCA) possesses exceptional optical properties and exhibits pressure‐sensitive adhesion, making it widely utilized in the adhesive layers of various electronic display devices. However, the increasing popularity of foldable mobile phones in recent years has imposed new requirements on the overall performance of OCA. Conventional pressure‐sensitive adhesives can enhance recoverability through cross‐linking but often demonstrate inadequate adhesive strength. In this study, three long‐chain crosslinking agents (CL) were synthesized using hydroxyethyl acrylate (HEA), dicyclohexylmethane diisocyanate (HMDI), polypropylene glycol (PPG), polyether amine (PEA), and hydroxyl‐terminated polybutadiene (R45V). The long‐chain CL agent contains numerous flexible segments that improve the recovery capability of the OCA while maintaining a certain level of adhesion. The optical clear pressure‐sensitive adhesive, crosslinked by three flexible crosslinkers, exhibits a low glass transition temperature (−60 to −40°C) and a low storage modulus (<0.1 MPa), along with an appropriate 180° stripping force (6–8 N/25 mm). Optically transparent pressure‐sensitive adhesives demonstrate excellent recovery properties (>85%), high light transmittance (>92%), and exceptional flexibility. Moreover, compared to market products, the optically transparent pressure‐sensitive adhesive shows superior folding resistance (>100,000 times). This indicates its suitability for applications in flexible optical displays such as foldable mobile phones and wearable electronics.

Pseudomorphic synthesis of pore size-tunable mesoporous silica spherical particles and their application for the fraction of low-molecular-weight heparin.

In this study, spherical silica with pore size varied from 30 to 200 Å was synthesized by pseudomorphic transformation at atmospheric pressure. 40-80 Å silica particles with a narrow pore distribution were obtained by using quaternary amine cationic surfactants and different kinds of swelling agents, including polypropylene glycol, 1,3,5-trimethylbenzene, alkanes, and alkanols. Alkyl imidazolium ionic liquid surfactants were used to synthesize large pore size distribution silica spheres with pore sizes in the range of 110-200 Å. All these silica particles can be synthesized under mild conditions within 12h, which provides a facile synthesis method for the preparation of a chromatographic matrix with tunable pore size. The method is reproducible and the relative standard deviation of silica sphere pore structure parameters in scaled-up preparations is less than 6%. The pore size on the fraction of low-molecular-weight heparin (LMWH) was investigated in size exclusion chromatography. Matrixes with different pore size distributions have various size exclusion regions. By using UPS-60-Diol columns in a twin-column recirculation separation process, LMWH with>85% heparin with molecular weight within the range of 3000-8000Da were separated in five-column volumes.

Oxyethylated polypropylene glycols of various structures as surfactants for the synthesis of polystyrene and polymethyl methacrylate suspensions with a narrow particle size distribution

Oxyethylated polypropylene glycols of various structures as surfactants for the synthesis of polystyrene and polymethyl methacrylate suspensions with a narrow particle size distribution

Practical Osmotic Agent for High-Degree Pharmaceutical Pre-Concentration by Organic Solvent Forward Osmosis.

Pre-concentration can reduce the total production costs in the pharmaceutical industry. Organic solvent forward osmosis (OSFO) is a suitable pre-concentration method because of its nonthermal nature, low capital cost, and potential for achieving high-degree concentrations. In a previous study, we first demonstrated a high-degree OSFO concentration. Sucrose octaacetate (SoA) in MeOH was concentrated to 52 wt% using polyethylene glycol (PEG)-400 as the osmotic agent, but the concentrated solution had a concentration of 17% PEG-400 because of the reverse solute flux. This result does not meet the typical purity standards required for pharmaceutical production, indicating the need to determine a suitable osmotic agent that can be used for practical purposes. This study proposes a practical osmotic agent for OSFO pre-concentration. First, osmotic agents were screened from a practical perspective. Polypropylene glycol (PPG)-400 was selected, owing to its low toxicity, good solubility, and low viscosity. Subsequently, the OSFO concentration was demonstrated using PPG-400 as the osmotic agent. SoA in MeOH was concentrated from 9.4 wt% to 48 wt%. The final feed solution contained only 0.04 wt% PPG-400. This result is the first demonstration of successful pharmaceutical pre-concentration using OSFO that satisfies the typical purity requirement in pharmaceutical production.

Self‐healing reversible network from furfuryl‐functionalized copoly(triazine‐r‐polypropylene glycol‐r‐polydimethylsiloxane)

AbstractNew shape‐memory networks composed of both reversible Diels–Alder covalent crosslinks and the hydrogen and π–π stacking bonds of triazine functional groups, with self‐healing properties as a result of the reversibility of these dynamic bonds were achieved from a furfuryl‐functionalized copoly(triazine‐r‐polypropylene glycol‐r‐polydimethylsiloxane), crosslinked with a maleimide end‐capped polycaprolactone and a long polycaprolactone‐based chain extender. The presence of multiple dynamic bonds, including the Diels–Alder and triazine‐derived π–π stacking and H‐bond interactions as well as the enhanced network mobility arising from polypropylene glycol, polydimethylsiloxane and polycaprolactone segments upon triggering the shape memory effect resulted in a material with high toughness (~200 MPa J−1) and efficient healing ability (with a recoveries of tensile strength and toughness after being cut and healed of 87% and 94%, respectively).Highlights Furfuryl dichlorotriazine was coupled with PPG and PDMS forming a copolymer. The copolymer was crosslinked with PCL‐dimaleimide and PCL‐difuran extender. Multiple dynamic bonds (Diels–Alder, π–π stacking and H‐bond) were present. The network showed high toughness and good healing performance.

Experimental Investigations on Shear Thickening Fluids as "Liquid Body Armors": Non-Conventional Formulations for Ballistic Protection.

Shear thickening fluids (STFs) have garnered attention as potential enhancers of protective capabilities and for the optimization of Kevlar® armor design. To assess the possible shear thickening properties and potential application in ballistic protection, ten formulations were developed by employing polyethylene glycol (PEG) or polypropylene glycol (PPG), along with fumed silica or Aerosil HDK®. Rheological characterization facilitated the identification of formulations displaying shear thickening behavior. The potential integration of the selected shear thickening fluids (STFs) into Kevlar®-based composites was investigated by studying the impact resistance of Kevlar® soft armor structures. Also, high-velocity impact testing revealed that the distance between aramid layers plays a crucial role in the impact resistance effectiveness of Kevlar®-STF composite structures and that there is a very narrow domain between optimal and undesired scenarios in which STF could facilitate the penetration of Kevlar. The introduction of STF between the Kevlar sheets disrupted this packing and the energy absorption capacity of the material was not improved. Only one formulation (PEG400, Aerosil 27 wt.%) led to a less profound traumatic imprint and stopped the bullet when it was placed between layers no.1 and no.2 from a total of 11 layers of Kevlar XP. These experimental findings align with the modeling and simulation of Kevlar®-STF composites using Ansys simulation software (Ansys® AutoDyn 2022 R2).

THE EFFECT OF CHEMICAL STRUCTURE OF VINYL CHLORIDE BASED POLYMERS ON ITS THE COMPATIBILITY WITH POLYURETHANEUREA ELASTOMER

The effect of the chemical structure of vinyl chloride-based polymers, such as poly(vinyl chloride) (PVC), chlorinated PVC (cPVC), vinyl chloride/vinylidene chloride copolymer VCVD-40TM, vinyl chloride/vinyl acetate copolymer А-15TM on its compatibility with poly(ether-urethane)urea elastomer (PUU) was studied by DSC and FTIR spectroscopy. The segmented PUU was synthesized by prepolymer approach in N,N-dimethylformamide (DMF) solution using poly(propylene glycol) of number-averaged molecular weight (Mn) of 1000 Da, 2,4-tolylenediisocyanate and tolylene 2,4-diamine as a chain extender at a molar ratio of 1:2:1. PUU/vinyl chloride-based polymer blends was prepared by solution casting technique vie DMF solution. It was found a compatibility of PUU based blends containing 30 % PVC (PUU/30PVC blend) or cPVC (PUU/30cPVC) were initiated by strong hydrogen bonding. As a result, the blends are characterized by single wide relaxation transition. A glass transition temperature (Тс) of PUU/30PVC composite is similar to the theoretical one (ТFс), which is calculated using the Flory-Fox equation, whereas Тс value of PUU/30cPVC composite is higher than ТFс. Introducing polar vinyl acetate or vinylidene chloride fragments into vinyl chloride-based polymer macrochains suppresses the compatibility of components of the polymer blends and initiates the formation of a biphase microheterogeneous structure. The formation of intermolecular hydrogen bonding network at the interface in polymer-polymer blends is confirmed by FTIR spectroscopy. Comparative analysis of experimental and theoretically calculated (additive) tensile characteristics of polymer blends demonstrates their substantial dependence on interface interactions between the constituents. The highest strengthening effect was observed for cPVC or PVC-containing nanocomposites.