Colloidal Particles Research Articles

Confined Gelation Synthesis of Flexible Barium Aluminate Nanofibers as a High-Performance Refractory Material.

Barium aluminate (BAO) ceramics are highly sought after as a kind of high-temperature refractory material due to their exceptional thermal stability in both vacuum and oxygen atmospheres, but their inherent brittleness results in rapid hardening, imposing a negative impact on the overall construction performance. Here, we report a strategy to synthesize flexible BAO nanofibers with a needle-like structure through confined-gelation electrospinning followed by in situ mineralization. The confined gelation among the colloidal particles promotes the formation of precursor nanofibers with high continuity and a large aspect ratio. The resulting flexible BAO nanofiber membranes are bendable, stretchable, and can even be woven, exhibiting a softness (12 mN) that is lower than that of tissue paper (27 mN). Additionally, they are capable of withstanding hundreds to thousands of continuous buckling and bending at 50% deformation without tearing. More importantly, the low emissivity of the flexible BAO nanofiber membranes ensures excellent thermal insulation at 1300 °C while preserving structural integrity and performance stability. In this sense, our strategy can be easily scaled up to produce flexible yet tough oxide ceramic membranes for a wider range of applications.

Reduction of organic matter and disinfection by products formation at surface water treatment plants in Egypt

ABSTRACT Although the removal of colloidal particles continues to be an important reason for using coagulation, currently a newer approach, the removal of organic matter to reduce the formation of disinfection byproducts (DBPs) such as trihalomethanes (THMs) are suspected carcinogens. Inefficient removal of total organic carbon (TOC) leads to the formation of carcinogenic THMs. This motivates the research efforts to find a way to reduce them in potable water. The first objective of this research is monitoring the water quality (raw and produced) for selected three water treatment plants within Giza Governorate to reveal the most polluted site (high TOC in the raw water and THMs in the treated water) in the study areas. The second objective of this study is enhancing coagulation to reduce TOC and THMs from surface water treating. In this study, two different coagulants aluminum sulfate (alum), and ferric chloride were tested under different conditions of pH and coagulant concentration to determine their effectiveness for removal of TOC, THMs and turbidity. Optimum values for the mentioned conditions were used to achieve the maximum reduction for TOC and THMs in Al-Ayat drinking water treatment plant (DWTP) which recorded the highest concentration of TOC and THMs. Ferric chloride as a coagulant achieved the maximum removal percentage % of TOC, THMs and turbidity as 79%, 82% and 94%, respectively, at ferric chloride dose 100 mg/L, while alum as a coagulant recorded the maximum removal percentage % of TOC, THMs and turbidity as 46%, 52% and 91%, respectively, at alum dose 100 mg/L. The results indicated that ferric chloride as a coagulant has the highest efficiency reduction of TOC, THMs and turbidity if compared to alum with the same dose added.

High-efficiency synthesis of colloidal silica via suppression of foam layer

As an important fundamental material, colloidal silica is widely used in many fields. Hydrolysis of elemental silicon is an important method for the preparation of colloidal silica. This method has been widely studied because of its simple process, low cost, easy control of colloidal particle size and good stability. However, this method has the problem of low reaction conversion rate (RCR). This paper proposed an efficient method to increase RCR of colloidal silica by inhibiting the formation of a foam layer. After the size of the silicon powder particle, reaction time, and the defoamer types were optimized, the defoamer of hydrophobic fumed silica could effectively inhibit the increase of foam layer and improve the yield of colloidal silica, the RCR was significantly increased from 54.8 % to 85 % within 4 h. This research provides an innovative strategy for the efficient chemical synthesis of colloidal silica.

Nanomaterials Marvels: Transformative Advancements in Biomedicine, Drug Delivery, and Pharmaceutical Analysis

Nanoparticles are solid colloidal particles ranging in size from 10 to 1000 nm having high surface area-to-volume ratio which allows them for efficient interaction with biological systems. Nanoparticles offer many benefits in comparison to larger particles such as increased surface-to-volume ratio and increased magnetic properties. Nanomaterials hold the potential to revolutionize in critical domains like Biomedicine, Drug Delivery, and Pharmaceutical Analysis. These particles can be functionalized with specific molecules to target diseased cells or tissues, enhancing the efficacy of drugs while minimizing side effects. For instance, gold nanoparticles conjugated with antibodies can be used for targeted cancer therapy, delivering therapeutic agents directly to tumor cells. Similarly drugs encapsulated within nanoparticles can be protected from premature degradation and released in a controlled manner at the target site improving their drug solubility, and enhance cellular uptake, leading to better therapeutic effect in treatment strategies. Polymeric nanoparticles, liposomes, and micelles are some examples of commonly used nanocarriers for drug delivery. Nanomaterials are finding increasing applications in pharmaceutical analysis and can be employed as highly sensitive detection probes for drugs, metabolites, and biomarkers. Additionally, nanomaterials can be used for the separation and purification of bio molecules, facilitating accurate and efficient analysis. This review explores different types of nano materials used exploring their new advances and applications in biomedicine, drug delivery, and pharmaceutical analysis. As research continues to overcome current challenges, nanomaterials unique properties hold immense promise for revolutionizing healthcare and improving patient outcomes.

Calciprotein particles induce arterial stiffening ex vivo and impair vascular cell function

Calciprotein particles (CPPs) are an endogenous buffering system, clearing excessive amounts of Ca2+ and PO43- from the circulation and thereby preventing ectopic mineralization. CPPs circulate as primary CPPs (CPP1), which are small spherical colloidal particles, and can aggregate to form large, crystalline, secondary CPPs (CPP2). Even though it has been reported that CPPs are toxic to vascular smooth muscle cells (VSMC) in vitro, their effect(s) on the vasculature remain unclear. Here we have shown that CPP1, but not CPP2, increased arterial stiffness ex vivo. Interestingly, the effects were more pronounced in the abdominal infrarenal aorta compared to the thoracic descending aorta. Further, we demonstrated that CPP1 affected both endothelial and VSMC function, impairing vasorelaxation and contraction respectively. Concomitantly, arterial glycosaminoglycan accumulation was observed as well, which is indicative of an increased extracellular matrix stiffness. However, these effects were not observed in vivo. Hence, we concluded that CPP1 can induce vascular dysfunction.

Development of Solventless Pharmaceutical Technique for Manufacture of Pharmaceuticals

The aim of our study was to develop a solventless drug pelletization and polymer coating technique for pharmaceutical manufacturing. This review describes a dry coating technique using a mechanical powder processor and a V-shaped blender to produce coated pellets or tablets by mechanically mixing polymer particles and core materials (such as drug pellets and uncoated tablets) without the need for a solvent. First, aqueous latexes comprising colloidal polymethacrylates and ethylcellulose were solidified by freeze drying to produce polymer particles for the dry coating process. These particles and the cores were then subjected to mechanical powder processing or V-shaped blending to provide coated formulations with controlled-release characteristics. Polymer coating was achieved by using agglomerates comprising assembled colloidal polymer. The agglomerated polymer was easily pulverized during the mixing treatments due to its loose structure (the lack of close contacts between the colloidal particles), and the resulting fine polymer with high adhesiveness was deposited on the cores. Colloidal polymer dispersed in aqueous latex tends to coagulate in the freeze-drying process due to condensation of the dispersion, yielding dense agglomerates with poor coating characteristics. The presence of surfactants (such as sodium lauryl sulfate) in the latex can prevent adhesion between colloidal particles in the freeze-drying process, providing loosely structured agglomerates suitable for dry coating. Dry coating with a V-shaped blender could thus be achieved with these polymer particles instead of having to use a mechanical powder processor.

Colloidal particles as noise source for random number generation

In this work, we investigate colloidal particle patterns as a possible noise source for random number generation. We systematically analyze the minimum entropy of the noise source over different particle concentrations of {1, 3, 5, 7, 10, 12, 15} mg/ml according to the recommendations of the National Institute of Standards and Technology Special Publication 800-90B. The estimated minimum entropy of the non-independent and identically distributed particle pattern noise source is Hmin = 0.5896/1 bit at a particle amount of 5 mg/ml. For further entropy extraction on the noise source data, the secure hash algorithm is used to construct an entropy source. The randomness of the derived entropy source is verified according to the National Institute of Standards and Technology Special Publication 800-22 Rev. 1a and the accompanying statistical test suite. The entropy source passes all randomness tests of the statistical test suite and shows an estimated minimum entropy of Hmin = 0.9992/1 bit.

Water-Enhancing Gels Exhibiting Heat-Activated Formation of Silica Aerogels for Protection of Critical Infrastructure During Catastrophic Wildfire.

A promising strategy to address the pressing challenges with wildfire, particularly in the wildland-urban interface (WUI), involves developing new approaches for preventing and controlling wildfire within wildlands. Among sprayable fire-retardant materials, water-enhancing gels have emerged as exceptionally effective for protecting civil infrastructure. They possess favorable wetting and viscoelastic properties that reduce the likelihood of ignition, maintaining strong adherence to a wide array of surfaces after application. Although current water-enhancing hydrogels effectively maintain surface wetness by creating a barricade, they rapidly desiccate and lose efficacy under high heat and wind typical of wildfire conditions. To address this limitation, unique biomimetic hydrogel materials from sustainable cellulosic polymers crosslinked by colloidal silica particles are developed that exhibit ideal viscoelastic properties and facile manufacturing. Under heat activation, the hydrogel transitions into a highly porous and thermally insulative silica aerogel coating in situ, providing a robust protective layer against ignition of substrates, even when the hydrogel fire suppressant becomes completely desiccated. By confirming the mechanical properties, substrate adherence, and enhanced substrate protection against fire, these heat-activatable biomimetic hydrogels emerge as promising candidates for next-generation water-enhancing fire suppressants. These advancements have the potential to dramatically improve the ability to protect homes and critical infrastructure during wildfire.

Effect of particle stiffness on microgel self-assembly and suspension phase behavior over a broad temperature range

We synthesized thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) colloidal microgel particles of different stiffnesses by controlling the concentration of a polar crosslinker in a precipitation polymerization synthesis method. When suspended in an aqueous medium, the particles collapsed by expelling water as the temperature was raised toward the volume phase transition temperature (VPTT) of ≈ 34 °C. We noted that the sizes of the stiffer particles, synthesized with higher crosslinker concentration, collapsed less abruptly. Using Fourier transform infrared spectroscopy, we observed enhanced particle dehydration with increasing temperature and decreasing particle stiffness. Oscillatory rheology experiments on dense aqueous PNIPAM suspensions, prepared at a fixed particle effective volume fraction ϕeff = 1.5 at 25°C, revealed that suspensions constituted by the stiffest particles are the most elastic over a broad temperature range. Above the VPTT, suspensions of particles of intermediate stiffnesses exhibited two-step yielding, a typical signature of fragile gel formation. Zeta potential measurements showed that PNIPAM particles of lower stiffnesses are rendered electrostatically unstable in aqueous suspension. Combining cryogenic scanning electron microscopy and rheology, we noted a glass–glass transition when the temperature of a dense suspension of stiff PNIPAM particles was raised across the VPTT. In contrast, suspensions of particles of the lowest stiffnesses showed a gel-viscoelastic liquid–gel transition during an identical temperature ramp experiment. Our study reveals that temperature-induced phase transformations in dense PNIPAM suspensions depend sensitively on the stiffness of the constituent particles and can be explained by considering amphiphilicity-driven morphological changes in the suspension microstructures.

Nonequilibrium probability currents in optically-driven colloidal suspensions

In the absence of directional motion it is often hard to recognize athermal fluctuations. Probability currents provide such a measure in terms of the rate at which they enclose area in the reduced phase space. We measure this area enclosing rate for trapped colloidal particles, where only one particle is driven. By combining experiment, theory, and simulation, we single out the effect of the different time scales in the system on the measured probability currents. In this controlled experimental setup, particles interact hydrodynamically. These interactions lead to a strong spatial dependence of the probability currents and to a local influence of athermal agitation. In a multiple-particle system, we show that even when the driving acts only on one particle, probability currents occur between other, non-driven particles. This may have significant implications for the interpretation of fluctuations in biological systems containing elastic networks in addition to a suspending fluid.

COPOLYMER BASED ON [(3-METHACRYLOYLAMINO)PROPYL] TRIMETHYLAMMONIUM CHLORIDE AS A FLOCCULANT FOR INDUSTRIAL WATER TREATMENT

The using of polymeric flocculants in the development of the oil industry in Kazakhstan is one of the innovative tasks. Therefore, the creation of new effective flocculants based on available industrial monomers with structure-forming is an urgent task. The mechanism of action of flocculants is based on the phenomenon of adsorption of flocculant molecules on the surface of colloidal particles, the formation of a network structure of flocculant molecules, and the adhesion of colloidal particles due to van der Waals and other forces. New polymeric flocculant with different molar composition was synthesized by radical copolymerization [(3-methacryloylamino)propyl]trimethylammonium chloride (TMAPMACh) with N,N-dimethyl-acrylamide (DMAA) at 333 K in the presence of ammonium persulfate, (NH4)2S2O8 as an initiator. The molar composition of the synthesized TMAPMACh-DMAA copolymer was determined by FTIR and NMR spectroscopy and conductometric titration with AgNO3 solution. The flocculation properties of the copolymers were studied by measuring the sedimentation of dispersed particles of bentonite suspension in the presence of the flocculant. Sedimentation degree was determined by measuring the optical density of the suspension. It was found that TMAPMACh-DMAA copolymers had a flocculating effect and could be used for industrial wastewater treatment. Thermogravimetric analysis showed that this copolymer was thermally stable up to 270°C. Therefore, it can be used in deep well drilling to regulate the properties of drilling fluids.

Fe (hydr)oxides and organic colloids mediate colloid-bound chromium mobilization in Cr(VI) contaminated paddy soil

The association of chromium (Cr) with colloidal particles transport in contaminated sites can affect hexavalent chromium (Cr(VI)) migration and transformation, which is an important mechanism for Cr pollutants in soil and groundwater systems. Here, we investigated colloid and particle-bound Cr migration and transformation effects on rice Cr accumulation during different rice growth stages and different redox conditions in Cr(VI) contaminated soil by pot experiment. Results showed that 13–29% of soil Cr was water dispersible colloid-bound (100–1000 nm) form during rice growth. Using transmission electron microscopy - energy dispersion spectroscopy and asymmetric flow field - flow separation, we identified colloid-bound organic matter (OM) and iron (Fe), most likely in the form of Fe (hydr)oxides - clay composites, as the primary Cr carrier. Specifically, colloid-bound Cr was mainly associated with 125–350 nm soil particle size. Under different redox conditions, colloid- and nanoparticle-bound Cr concentration decreased with increasing nanoparticles zero-valent iron (nZVI) dose. Soil reoxidation promoted the colloid- and nanoparticle-bound Cr release due to the weakly crystalline Fe-(hydr)oxides reprecipitation. Further quantitative analysis showed that colloid-bound Cr concentrations were positively correlated with colloid-bound Mn concentrations during the whole rice growth soils. Most important of all, Cr content in rice grain was positively correlated with colloid-bound Cr significantly. This study provides a quantitative and size-resolved understanding of particle-bound Cr in paddy soils, highlighting the importance of colloid-bound Cr and Fe interactions in Cr geochemical cycle of paddy soil.

Achieving liquid processors by colloidal suspensions for reservoir computing

The increasing use of machine learning, with its significant computational and environmental costs, has motivated the exploration of unconventional computing substrates. Liquid substrates, such as colloids, are of particular interest due to their ability to conform to various shapes while exhibiting complex dynamics resulting from the collective behaviour of the constituent colloidal particles. This study explores the potential of using a PEDOT:PSS colloidal suspension as a physical reservoir for reservoir computing in spoken digit recognition. Reservoir computing uses high-dimensional dynamical systems to perform tasks with different substrates, including physical ones. Here, a physical reservoir is implemented that encodes temporal data by exploiting the rich dynamics inherent in colloidal suspensions, thus avoiding reliance on conventional computing hardware. The reservoir processes audio input encoded as spike sequences, which are then classified using a trained readout layer to identify spoken digits. Evaluation across different speaker scenarios shows that the colloidal reservoir achieves high accuracy in classification tasks, demonstrating its viability as a physical reservoir substrate.

The Particle Drifting Effect: A Combined Function of Colloidal and Drug Properties.

The particle drifting effect, where nanosized colloidal drug particles overcome the diffusional resistance of the aqueous boundary layer adjacent to the intestinal wall and increase drug absorption rates, is drawing increasing attention in pharmaceutical research. However, mechanistic understanding and accurate prediction of the particle drifting effect remain lacking. In this study, we systematically evaluated the extent of the particle drifting effect affected by drug and colloidal properties, including the size, number, and type of the moving species using biphasic diffusion experiments combined with computational fluid dynamics simulations and mass transport analyses. The results showed that the particle drifting effect is a sequential reaction of particle dissolution/dissociation in the diffusional boundary layer, followed by absorption of the free drug. Therefore, factors affecting the rate-limiting step, which can be either process or both under different circumstances, alter the particle drifting effect. Experimental results also agree with the theory that the particle dissolution rate is dependent on particle size, concentration, and drug solubility. In addition, rapid bile micelle dissociation and bile salt absorption facilitated drug absorption by the particle drifting effect. Our findings explain the highly dynamic nature of the particle drifting effect and will contribute to rational formulation development and better bioavailability prediction for formulations containing colloidal particles.

Colloid mobilization and transport in response to freeze-thaw cycles: Insights into the heavy metal(loid)s migration at a smelting site

Smelting sites often exhibit significant heavy metal(loid)s (HMs) contamination in the soil and groundwater, which are inevitably subjected to environmental disturbances. However, there is limited information available regarding the migration behaviors of HMs in a disturbed scenario. Thus, this work explored the migration of HMs-bearing colloids in response to freeze-thaw treatments by laboratory simulation and pore-scale study. Ultrafiltration results of soil effluents revealed that 61.5 %, 47.6 %, 68.0 %, and 59.2 % of Zn, Cd, Pb, and As were present in colloidal phase, and co-transported during treatments. Nanoparticle tracking analysis (NTA) further confirmed that freeze-thaw cycles were conducive to the generation of colloidal particles and showed the heteroagglomeration among different particles. Pore-network model (PNM) was used to quantify the soil macropore characteristics (macropore diameter, macropore number, coordination number, and Euler value) after treatments. It is evident that freeze-thaw cycles induced the formation of larger macropores while simultaneously enhancing macropore connectivity, thereby establishing an optimal pathway for colloid migration. These findings underscored the importance of environmental disturbances as a trigger for the release and migration of HMs in the smelting site, offering valuable insights for controlling HMs pollution. Environmental implicationThe contaminated site has been subjected to prolonged environmental disturbances, causing the exacerbation of pollutants leaching and frequent occurrences of unstable pollution situations. This work explored the migration of HMs-bearing colloids in response to freeze-thaw treatments by laboratory simulation and pore-scale study. The distinct effects of freeze-thaw treatment on colloidal particle number concentration and macropore characteristics may explain the generation and migration of colloid-associated HMs driven by environmental disturbances. This work revealed the underlying mechanisms driving the redistribution of HMs under freeze-thaw cycles, offering valuable insights for risk assessment of soil and groundwater associated with HMs migration.

Effect of fat replacement in high internal phase emulsions constructed by high temperature saccharification of grafted proteins on gel properties and flavor profiles of sausages

In order to mitigate the risk of cardiovascular diseases associated with excessive saturated fatty acid intake, utilizing high internal phase emulsions (HIPEs) as a substitute for animal fat in producing high-quality fat-substituted meat products is an ideal approach. This study involves the preparation of glycosylation products of egg white protein (EWP) through saccharification at high temperatures in the presence of fructooligosaccharides (FO). The resulting glycation products of EWP were employed to create colloidal particles, forming HIPEs, which were further utilized to induce the formation of HIPEs gels (HIPEs-Gs). The study investigated the effects of substituting different ratios (25%, 50%, 75%, and 100%) of animal fat with HIPEs and HIPEs-Gs on the gel properties and flavor characteristics of sausages. Results showed that, compared to the control group, substituting fat with HIPEs significantly improved the gel properties, cooking yield, and G' of sausages, while excessive HIPEs-Gs substitution yielded negative effects. Low-field nuclear magnetic resonance results also demonstrated that adding HIPEs improved water and oil distribution in the sausage batter, enhancing protein's binding capacity with water. Scanning electron microscope revealed that HIPEs substitution led to a denser gel network with smaller pores, effectively "locking in" more water. Analysis of volatile compounds indicated accelerated release of aromatic compounds, alkanes, sulfides, and lipids when fat was substituted with HIPEs and HIPEs-Gs. Electronic tongue analysis suggested that HIPEs-Gs substitution reduced response values for umami and saltiness. In conclusion, compared to HIPEs-Gs, using HIPEs as a fat substitute improves the quality of sausages.

Convective assembly of silica colloidal particles inside photonic integrated chip-based microfluidic systems for gas sensing applications.

Optofluidics is a new field of modern science that stands at the interface of microfluidics and photonics and has good prospects for application in gas sensors. Microfluidics offers a promising platform for tuning and assembling monolayer structures that are used as sensitive layers for gas detection. Herein, we evaluate the concept of monolayer formation on a silicon nitride substrate enabling a surface coverage up to 59% through a microfluidic convective assembly and couple it with a photonic integrated chip to probe gas sensing performance.

Anomalous Diffusion and Non-Markovian Reaction of Particles near an Adsorbing Colloidal Particle

We investigate the diffusion phenomenon of particles in the vicinity of a spherical colloidal particle where particles may be adsorbed/desorbed and react on the surface of the colloidal particle. The mathematical model comprises a generalized diffusion equation to govern bulk dynamics and kinetic equations which can describe non-Debye relaxations and is used for the colloid’s surface. For the reaction processes, we also consider the presence of convolution kernels, which offer the flexibility of describing a single process or process with intermediate reactions before forming the final species. Our analysis focuses on analytical and numerical calculations to obtain the particles’ behavior on the colloidal particle’s surface and to determine how it affects the diffusion of particles around it. The solutions obtained show various behaviors that can be connected to anomalous diffusion phenomena and may be used to describe the ever-richer science of colloidal particles better.

The process of evaporation of a colloidal solution of stabilized Boron nitride nanoparticles

Purpose. Characterization of the chemical structure of boron nitride nanoparticles by IR spectroscopy during the evaporation of their colloidal system and their sizes by small-angle X-ray scattering.Methods. The solvent evaporation process from the colloidal system was studied using a Nicolet iS 50 FT-IR spectrometer in the mid-IR range (400 – 4000 cm-1), with an attenuated total reflectance accessory with a diamond crystal (incident angle of 45°) and a liquid cell (200 μL). The sizes of the colloidal particles were determined using an smallangle X-ray scattering diffractometer in linear collimation mode (resolution 0.03 nm-1, copper anode X-ray tube 2.2 kW, λ = 0.154 nm, exposure time 30 s).Results. The IR spectrum of boron nitride nanoparticles powder was measured, containing lines characteristic of cubic (952 cm-1) ) – c-BN and hexagonal crystalline phases (758, 1301, and 1372 cm-1) – h-BN. The average size of boron nitride nanoparticles in the colloidal system, according to small-angle X-ray scattering data, was 46 and 84 nm. The size of stearic acid, which acts as a stabilizing shell, was 0.8, 1.3, and 2.5 nm. Analysis of the IR spectra showed complete evaporation of the solvents (hexane and chloroform) from a drop of colloidal solution 1.2 mm thick within 30 minutes.Conclusion. In this work, the average sizes of boron nitride nanoparticles stabilized with stearic acid in a colloidal system were determined and the process of its evaporation was studied.

Модификация твердофазной полимерной поверхности путём прививки акриловых мономеров

Graft copolymerization onto a solid polymer surface is an effective tool for its modification. A large number of works have been published and require systematization. A search and review of English-language scientific literature devoted to the graft copolymerization of acrylic monomers onto a polymeric solid-phase surface have been carried out. Grafting onto plates and films, as well as fibers and colloidal particles, is considered. It has been revealed that the most popular substrates for graft copolymerization are, besides polyethylene, propylene and polyethylene terephthalate; polyurethanes, polyfluoroethylenes, rubbers, etc. Graft polymerization mainly proceeds on amorphous areas of the substrate and does not destroy the crystalline phase. It is possible to use the methods of controlled radical polymerization (ATRP, RAFT). Of the acrylic monomers, acrylic and methacrylic acids, glycidyl acrylate and glycidyl methacrylate, and others have been used, while the main method has been UV photopolymerization with an initiator–benzophenone. Of the three aliphatic ketones (acetone, methyl ethyl ketone and methyl propyl ketone), acetone has been the best solvent. Cophotoinitiators have been also used (a synergistic effect was observed), corona discharge, gamma radiation (60Co), ozone and plasma treatment, and a supercritical CO2 medium. The degree of grafting has been controlled by changing the soaking time in the monomer, pressure, concentration of monomer and initiator in the liquid phase, reaction temperature and reaction time. A new technology of graft polymerization with photopatterning has also been proposed. Problems of graft polymerization in terms of surface modification of polymer materials (hydrophilization of the surface, improving paintability and wettability, enhancing adhesion to certain surfaces, biocompatibility) are touched upon, and possible areas of their application are outlined.