Search Results (287)

Microplastics, MPs, plastic particles with dimensions between 0.1 and 5 mm, represent an important environmental pollutant. The removal of microplastics from natural and wastewater is a challenging research topic. In this regard, high-performance technical solutions must be identified, which can be based on existing treatment and purification technologies, to ensure their removal at concentration values in accordance with the legislation in force. In this study, the efficiency of removing some fractions of polyurethane microplastics, with dimensions smaller than 500 µm, from aqueous synthetic solutions with a concentration of 0.2 g L⁻¹, i.e., around 175 NTU, was evaluated. In the first stage of the study, the doses of coagulants and flocculants effective for the removal of microplastics were identified through the Jar Test. The variation in turbidity and their removal efficiencies were evaluated in the presence of classic coagulants, such as aluminum sulfate, Al₂(SO₄)₃·18H₂O, SA; iron sulfate (ferrous sulfate), FeSO₄, IS; polyaluminum chloride, [Al₂(OH)_nCl_6−n], PAC; Aloe Vera, AV, a flocculant; and activated carbon, AC, of the Norit GAC 830 W type. Classic coagulants, such as aluminum sulfate, have a good efficiency in removing microplastics, being able to provide a residual turbidity in the range of 6–10 NTU after a retention time of 50–60 min. In the second stage of the study, the removal efficiency of microplastics was tested using a laboratory pilot plant—called in the study the Smart Decantation-Filtration System, SDFS. The efficiency of the decanter was studied using Response Surface Methodology (RSM) to identify mathematical models that characterize the influence of key process variables: flow rate (A), microplastic size (B) and aluminum sulfate concentration (C) on microplastic removal efficiency. Sedimentation in the specially constructed decanter can raise the optimal value of the removal efficiency of polyurethane microplastics to 98.98%, and filtration can ensure an efficiency that reaches over 99.5%. Through this research, we aimed to identify viable solutions that can be applied to remove microplastics, MPs, from natural and wastewater. A novel element is the fact that we chose to study the removal of polyurethane, which is studied little in the literature. We identified the optimal doses of coagulants and flocculants that help sedimentation of MPs. The efficiency of an installation called Smart Decantation-Filtration System, specially designed to ensure increased efficiency in the removal of microplastics, was determined. The results obtained were encouraging. Full article

As power equipment insulation materials, epoxy resin and phenolic resin are inevitably exposed to damp-heat environments during long-term operation, leading to ageing degradation. This study systematically investigates the effects of damp-heat ageing (85 °C, 90% RH, 0–56 days) on the flame retardancy of both resins through oxygen index tests, vertical combustion experiments, and microstructural analysis (SEM/EDS). Results indicate that ageing unexpectedly enhances flame retardancy: Epoxy resin: Oxygen index rapidly increased from 64.4% (0 days) to 76.5% (21 days), then stabilised at 75–76%. Afterflame time decreased from 143 s to 109 s after 56 days. Phenolic resin: Oxygen index rose continuously with ageing; afterflame time dropped sharply from 211 s (0 days) to 0 s (56 days). Mechanistic analysis reveals that ageing promotes surface enrichment of flame-retardant elements (Ca, Mg, Si in epoxy; Al, Mg in phenolic) and structural changes (e.g., porous carbonisation), which facilitate barrier effects against heat/oxygen diffusion. This work challenges conventional views on ageing-induced degradation, providing new insights for evaluating insulation safety in humid environments. Full article

The selective removal of beryllium from aqueous matrices remains a critical environmental and industrial challenge due to beryllium’s extreme toxicity, strong hydration chemistry, and the difficulty of separating Be²⁺ from chemically similar cations such as Al³⁺. In this study, a novel multidentate Schiff-base porous organic adsorbent, TFP-HEDA, was synthesized by condensation of 2,4,6-trihydroxybenzene-1,3,5-tricarbaldehyde (TFP) with N-(2-hydroxyethyl)ethylenediamine (HEDA) followed by urethane post-functionalization and systematically characterized by FTIR, ¹H/¹³C NMR, MALDI-TOF MS, elemental analysis, BET surface area analysis (617 m² g⁻¹), PXRD, and XPS. Batch adsorption experiments demonstrated rapid Be²⁺ uptake, achieving 90% removal within 20 min and equilibrium within 30 min. Among the isotherm models evaluated, the Langmuir model yielded the highest statistical consistency (R² = 0.9835, RMSE = 5.15 mg g⁻¹, χ² = 1.137) with a predicted maximum adsorption capacity of 163.93 mg g⁻¹ agreeing closely with the experimental value of 163.67 ± 6.42 mg g⁻¹ (deviation < 0.2%); this mathematical adequacy is interpreted as compatibility with a finite, saturable set of inner-sphere coordination sites rather than confirmation of a flat, energetically uniform surface, with chemisorption independently and more rigorously established by Dubinin–Radushkevich analysis (E = 28.87 kJ mol⁻¹) and post-adsorption FTIR and XPS evidence. Dubinin–Radushkevich analysis confirmed a chemisorption mechanism with mean adsorption energy E = 28.87 kJ mol⁻¹, consistent with inner-sphere Be²⁺–O/N coordination. Process optimization using response surface methodology based on a central composite design achieved 99% Be²⁺ removal at pH 5, an adsorbent dose of 60 mg/20 mL, and a contact time of 30 min (R² = 0.9892). Post-adsorption FTIR, XPS, BET, and TGA characterization confirmed framework integrity and the inner-sphere multidentate coordination mechanism. TFP-HEDA retained 82.4% of its initial capacity after nine adsorption–desorption cycles, demonstrating practical regenerability for Be²⁺ recovery applications. Full article

Lightweight high-entropy alloys are primarily designed to overcome the strength-to-density ratio limitations of conventional counterparts and often consist of elements with drastically different melting temperature and vapor pressure. Their chemistry, therefore, imposes challenges on alloy synthesis, particularly through liquid metal engineering routes, since elements with high vapor pressure (e.g., Mg, Zn, Li) vaporize before the higher-melting-point ingredients (e.g., Cu, V, Ni) are fully molten, resulting in volatile element loss. To overcome this challenge, a novel pressure-assisted induction melting (PAIM) process was developed and the proprietary furnace for its implementation was designed and built. The system allows precision melting of up to 10 cm³ of an alloy at temperatures up to 1700 °C while addressing the partial pressure requirements during the melting progress. The chamber is prepared using rough vacuum and re-filled with inert gas such as argon with the operating pressure range from about 10⁻⁴ MPa up to maximum of 1.6 MPa (233 psi). The alloy chemical composition can be modified in situ by feeding solid additives at specific melting stages through the isolated airlock without disrupting the pressure conditions within the chamber. The viability of the concept was verified by synthesis of two lightweight non-equimolar high-entropy alloys: Mg-rich Mg₅₀(MnAlZnCu)₅₀ and Al-rich Al₃₅Mg₃₀Si₁₃Zn₁₀Y₇Ca₅. The experiments showed that sequential multi-step melting procedures, designed based on inputs from FactSage computational analysis, when combined with PAIM synthesis, allowed manufacturing fully dense and chemically homogenous complex alloy compositions with optimal volumes for materials discovery research. Full article

Wollastonite-1A from Băița Bihor occurs in distal calcic skarns developed in the contact zone of a mainly granodioritic batholith, of Upper Cretaceous age, with Mesozoic limestones and dolostones. Wollastonite generally occurs in the inner part of metasomatic columns, in monomineralic skarns or associated with grossular and molybdenite-2H as ore mineral. The physical properties (i.e., refraction indices α = 1.616, β = 1.629, and γ = 1.631, 2V_α = 39° and density D_m = 2.922(3) g/cm³) are typical for a term close to the stoichiometry, which is confirmed by the chemical analysis. The chemical structural formula of the analyzed wollastonite-1A is (Ca_1.000Mg_0.002Mn_0.001Fe_0.001)(Al_0.004Ti_0.001Si_0.994)O₃, which closely approximates the ideal CaSiO₃. The Gladstone–Dale compatibility indices account for an excellent agreement between physical and chemical data. The mineral can be satisfactorily refined as triclinic, space group $P\overline{1}$, with R₁ = 0.0678 and cell parameters a = 7.9233(3) Å, b = 7.3203(3) Å, c = 7.0651(3) Å, α = 90.053(3)°, β = 95.208(3)°, γ = 103.384(3)°. Both the IR and Raman spectra principally reveal bands related to vibrations of bridged and non-bridged oxygens pertaining to SiO₄ structural tetrahedra. At Băița Bihor, wollastonite-1A is part of the prograde paragenesis, marked by a peak temperature of 550–600 °C. Full article

Background/Objectives: MRI-guided neurovascular interventions could benefit from lower-field systems due to reduced magnetic and radiofrequency hazards. However, safety and practical visibility of commonly used neurointerventional devices at 0.55 T remain insufficiently characterized. We evaluated magnetic field interactions, RF-induced heating, and qualitative device visibility in 11 commercially available and commonly used neurovascular devices on a 0.55 T MRI system. Methods: Eleven devices, including stent retrievers, guidewires, catheters, and one embolization implant, were tested at 0.55 T. Magnetostatic interactions were quantified using the American Society for Testing and Materials (ASTM)-guided deflection methods for translational force (ASTM-F2052) and a two-string suspension apparatus for torque (adapted from Stoianovici et al.). RF-induced heating was measured in an in vitro perfused cerebral vessel phantom using a 15 min high-specific absorption rate spin echo sequence under static and flow conditions. Qualitative device visibility was assessed using a turbo spin echo (TSE) and balanced steady-state free precession (bSSFP) imaging on each device individually. Results: Eight of eleven devices passed the translational force test, while three devices (D, E, and G), containing significant ferromagnetic components, failed with deflection angles > 45°. Eight devices passed torque testing, remaining below the critical threshold in all rotation positions; three devices (D, G, and J) failed by exceeding the 54° criterion, including one guidewire and two devices with braided/coiled metallic structures. Under static conditions, RF-induced heating ranged from negligible to 10.4 °C (maximum in device D) and generally decreased under flow; in the flow configuration, temperature rise remained below 2 °C for 6/11 devices. Qualitative imaging performance differed by sequence, with bSSFP enabling improved delineation of device structure (best for devices A, C, and H), whereas devices D, E, F, and J produced extensive signal voids that precluded reliable visualization in both sequences. Overall, three devices satisfied all safety criteria while remaining clearly visible under MRI. Conclusions: Devices that pass safety thresholds at 0.55 T can serve as candidates for further sequence optimization and preclinical workflow development, enabling the design of low-SAR, device-compatible imaging protocols tailored for neurointerventional workflows. These results provide key safety data supporting the feasibility of MR-guided neurovascular procedures at 0.55 T. Full article

High-temperature carburization (HTC, 950–1050 °C) has emerged as a pivotal low-carbon, energy-efficient manufacturing technology for gear steels, accelerating carbon diffusion for reducing processing cycles by over 60% while achieving significant energy savings and emission reductions. However, the inherent contradiction between HTC efficiency and microstructural stability, specifically austenite grain coarsening, severely degrades mechanical properties (e.g., strength, toughness, fatigue resistance) and limits widespread application. This review systematically synthesizes recent advances in austenite grain size regulation during HTC of gear steels, focusing on the core scientific framework of “grain coarsening mechanism—regulation strategy—performance enhancement”. It elaborates on thermodynamic and kinetic mechanisms of austenite grain growth, ripening behavior of microalloying precipitates (Nb(C,N), Ti(C,N), AlN, etc.), and their synergistic grain-refining effects. Comprehensive coverage of regulatory strategies (microalloying design, pretreatment technologies, process optimization, and integrated regulation) and characterization techniques is provided, along with a quantitative correlation between grain size, microstructure, and surface performance (wear resistance, corrosion resistance, and fatigue life). Numerical simulation and predictive models (empirical, theoretical, multiphysics coupling, machine learning-based) are critically analyzed, and current challenges (temperature-grain stability trade-off, multifactor synergy understanding, industrial scalability) and future research directions (advanced microalloying systems, intelligent process optimization, cross-scale modeling, green technology integration) are proposed. This review aims to provide theoretical guidance and technical support for optimizing the HTC performance of gear steels, catering to the demands of high-power-density transmission systems in automotive, aerospace, and heavy machinery industries. Full article

Leveraging fungal consortia to degrade heavy oil is an emerging strategy for mitigating/cleaning up environmental pollution. However, many consortia are predominantly evaluated by measuring the biodegradation efficiency of heavy oil, with insufficient attention paid to the mechanistic underpinnings and metabolic pathways. In this study, heavy oil-degrading fungal consortia were developed for potential application in soil bioremediation. Whole-genome sequencing was used to predict the metabolic pathways and interspecific interactions driving heavy oil biodegradation. Three heavy oil-degrading fungal strains, designated Aspergillus corrugatus FH2, Aspergillus terreus FL4, and Alternaria alstroemeriae FW1, were isolated from oil sludge in the Karamay Oilfield in Xinjiang, China. Four consortia were constructed through the combination of two or three strains. The consortium F13 (FH2 + FW1) achieved 72.0% removal of heavy oil in a simulated bioremediation test over 30 days, which was more efficient than other consortia and single strains (59.5–68.5%). Notably, the mean degradation rate of long-chain alkanes (C₂₄–C₂₈) by F13 reached 95.9%. After F13 treatment, the major fractions of heavy oil showed considerable degradation, 87.4% for saturates, 92.0% for aromatics, 69.5% for resins, and 27.3% for asphaltenes. Genome annotation of FH2, FL4, and FW1 revealed the presence of core genes for degradation of n-alkanes and aromatics, e.g., CYP505, frmA, fadB, hmgA, ALDH, and ACSL. These functional genes encoded cross-lineage enzymes, enabling synergistic catabolism of C₁₃–C₂₈ alkanes and aromatics. Our findings indicated that the fungal consortium of A. corrugatus FH2 and Al. alstroemeriae FW1 has remarkable bioremediation potential for heavy oil-contaminated sites. This study provides molecular evidence for the design of targeted interventions to improve soil remediation efficiency with fungal consortia. Full article

Selective laser melting (SLM), a pivotal additive manufacturing (AM) technology for titanium alloys, enables near-net-shape forming of complex structures with relative densities of up to 99.9%, making it indispensable in aerospace, biomedical, and marine engineering. This review comprehensively updates the state of the art on SLM-fabricated TC4 (Ti-6Al-4V) alloy, addressing critical gaps in previous studies by integrating novel research progress, in-depth mechanistic analyses, and multi-dimensional comparisons. The core focus is on the unique thermal cycle (10⁶–10⁸ °C/s heating/cooling rates) of SLM, which induces a predominant needle-like martensitic α′ phase (99.7%) and minimal β phase (0.3%), leading to intrinsic anisotropy and low ductility. Room-temperature tensile strength reaches 1315.32 MPa with 9.6% elongation, and high-cycle fatigue limits the range from 417 to 829 MPa, strongly dependent on process parameters and post-treatment. Corrosion anisotropy is systematically analyzed: the XY plane (parallel to scanning direction) exhibits superior corrosion resistance in 1 M HCl (fewer pits and lower corrosion current density) and 3.5% NaCl (more stable passive film) compared to the XZ plane (deposition direction). Novel insights include: (1) synergistic effects of SLM process parameters (laser power–scanning speed–hatch spacing) on defect evolution and microstructure uniformity; (2) atomistic mechanisms of α′→α + β phase transformation during post-heat treatment; and (3) corrosion–mechanical coupling behavior in harsh environments (e.g., marine and biomedical). Post-treatment strategies are refined: annealing at 800 °C for 2 h achieves 1099 MPa tensile strength and 17.4% elongation, while hot isostatic pressing (HIP) reduces porosity from 0.08% to 0.01% and weakens fatigue anisotropy. This review also identifies unresolved challenges (e.g., in situ defect monitoring and multi-field regulated performance) and proposes future directions (e.g., AI-driven process optimization and functional gradient structures). Full article

Earthen immovable cultural relics, such as murals and painted clay sculptures, are prone to deterioration (e.g., efflorescence, flaking, and cracking) under long-term preservation conditions. While conventional restoration materials primarily offer reinforcement, they fail to regulate the migration of soluble salts within the relics, which is the main cause of such damage. Herein, aimed at protecting the painted sculptures and murals of the Yungang Grottoes, nano calcium-aluminum layered double hydroxides (Ca-Al LDHs) were prepared, and their effectiveness in regulating salt crystallization within the earthen ground layer, as well as their reinforcement performance were investigated. Simulated salt crystallization tests revealed that coating the ground layer with Ca-Al LDHs delayed salt-induced damage time by 150%. This can be attributed to the ability of Ca-Al LDHs to adsorb sulfate ions from soluble salts, thereby inhibiting the crystallization of magnesium sulfate on the surface of the ground layer. After curing Ca-Al LDHs-coated samples at 35 °C and 55% relative humidity (RH) for 7 days, their surface Leeb hardness increased by 3.1%, and the weight loss rate (measured via tape peeling test) decreased by 38.3%. These results indicate that the surface bonding strength was enhanced following Ca-Al LDHs coating, with the underlying mechanism being the transformation of part of the LDHs into calcium carbonate under the influence of water and carbon dioxide. This study demonstrates that Ca-Al LDHs not only suppress magnesium sulfate crystallization but also provide effective surface consolidation, showing promising potential for application in conserving painted sculptures and murals at the Yungang Grottoes. Full article

Investigation of dialyzer thrombogenicity is a critical step during the development of a new dialyzer. Novel dialyzer membranes aim to reduce the inherent thrombogenic potential of artificial surfaces by, e.g., increasing membrane hydrophilicity. Reliable in vitro testing is fundamental during dialyzer development and must be in line with the current standards. Using the novel FX CorAL dialyzer with its increased membrane hydrophilicity as an example, this study characterizes dialyzer thrombogenicity in an in vitro test setup in line with ISO 10993-4 and identifies factors which influence dialyzer thrombogenicity. In a recirculation setup with human blood, platelet activation (platelet counts, β-thromboglobulin, platelet adsorption), coagulation (thrombin–antithrombin III complex) and complement activation (sC5b-9) were investigated among polysulfone- (FX CorAL, FX CorDiax, Optiflux, xevonta), polyethersulfone- (ELISIO, Revaclear, Theranova) and AN69 ST-based (Nephral) dialyzers. Additionally, the impact of dialysate and electrolyte composition on thrombogenicity was investigated. The FX CorAL showed the lowest platelet activation compared to all poly(ether)sulfone-based dialyzers and lower complement activation compared to most poly(ether)sulfone-based dialyzers and to the Nephral dialyzer. No significant differences were observed between the investigated dialyzers with regard to plasmatic coagulation. Among the tested parameters, the dialyzer showed the strongest impact on the thrombogenicity results. This study proposes guidance on in vitro testing of dialyzer thrombogenicity in line with current standards and may contribute to reducing the current heterogeneity among in vitro hemocompatibility testing. Full article

Mullite (Al₆Si₂O₁₃), an aluminosilicate with remarkable thermal and dielectric properties, is a promising material for advanced electronic applications. This study focuses on a sintered mullite composite and examines its structural, morphological, dielectric, and electrical properties. X-ray diffraction and scanning electron microscopy analyses confirm a well-defined crystalline structure and a homogeneous microstructure. Impedance spectroscopy measurements reveal a high relative permittivity at low frequencies, dominated by interfacial and jump polarization mechanisms. Electrical conductivity follows Jonscher’s double-power law, reflecting mixed ionic and electronic conduction due to contributions from grains and grain boundaries. Analysis of the Nyquist diagrams shows a marked decrease in resistances with increasing temperature: The grain resistance decreases from 21.87 MΩ to 4.85 MΩ, while that of the grain boundaries decreases from 89.44 MΩ to 5.94 MΩ between 450 °C and 900 °C. In addition, the relative permittivity increases sharply with temperature, from 25 × 10³ to 350 × 10³ at 1 kHz and from 200 to 1 × 10³ at 1 MHz over the same temperature range, highlighting the dominant influence of temperature and low frequencies on polarization mechanisms. These results confirm the strong potential of sintered mullite for electronic applications. The activation energy of the grain and grain boundary were determined to be E_a,g = 0.18 eV and E_a,bg = 0.22 eV, respectively. Full article

ZnO and CuO thin films were deposited separately using the radio frequency (RF) sputtering technique, and the effect of annealing in nitrogen and oxygen ambient environments was investigated. In this article, structural, optical, vibrational, and electrical characterizations were sequentially performed using techniques such as X-ray diffraction (XRD), UV–visible spectroscopy (UV-vis), Raman spectroscopy, photoluminescence (PL) spectroscopy, and current-voltage measurements using a DC four-probe station. XRD confirmed a high-crystallinity and wurtzite structure for ZnO, with the preferred orientation being along the c-axis (0001), and a monoclinic structure for CuO, with preferential orientation along the (002) axis. The absorption edges of the ZnO and CuO thin films were determined to be 3.24 eV and 2.89 eV, respectively. However, Urbach tails were observed only in the ZnO thin films, confirming the presence of localized Zn interstitials and oxygen vacancies. The absorption of CuO showed weak Urbach tails, suggesting that the defects were not localized. Raman spectroscopy performed on the ZnO and CuO thin films showed the appearance of weak E₂(high) and prominent A_g/B_2g modes, confirming the presence of ZnO and CuO bonding states, respectively. PL studies revealed room temperature emission for both the CuO and ZnO thin films, which is crucial for thin film solar cells and photodetectors. Two thin film heterostructures were fabricated with and without MoS₂ (a hole transport layer) on FTO substrates. The Al/FTO/CuO/ZnO/Al heterostructure revealed a rectifying behavior with a photo current of 2 mA in the dark, whereas light-induced characteristics resulted in a photocurrent of 5 mA. The Al/FTO/MoS₂/CuO/ZnO/Al heterostructure exhibited a similar rectifying behavior, with improved photo currents of 5 mA in the dark and 9 mA in the light. Full article

Austenitic Fe-Mn-Al-C lightweight steels have attracted considerable interest for automotive applications due to their exceptional specific strength, where κ-carbides precipitation critically influences mechanical properties. This review systematically examines the crystal structure, classification, and precipitation kinetics of κ-carbides, emphasizing their spatial distribution-dependent effects: coarse κ-carbides at austenite grain boundaries induce embrittlement and degrade toughness, while nanoscale κ’-carbides within grains enhance strength and ductility through dislocation interactions (e.g., Orowan bypassing and shearing), activating deformation mechanisms such as Dynamic Slip Band Refinement (DSBR), Shear Band-Induced Plasticity (SIP), and Microband-Induced Plasticity (MBIP). Thermodynamic calculations guide alloy design to ensure a single-phase austenite structure at the typical hot-rolling finishing temperature (~900 °C), avoiding harmful phases while promoting beneficial precipitates. Mn suppresses κ-carbide formation, whereas Al and C act as promoters, with intragranular κ’-carbides favoring higher Al/C concentrations (e.g., >6.2% Al and >1.0% C). Heat treatment parameters critically influence κ-carbide distribution, where rapid cooling (e.g., water quenching) suppresses κ-carbides, and subsequent aging (500–700 °C) enables homogeneous precipitation of κ’-carbides. Pre-deformation prior to annealing further accelerates κ-carbide nucleation by introducing crystal defects. Optimal performance requires integrated composition-processing-microstructure optimization to achieve a nnanoscaleκ’-carbide-strengthened austenite matrix through controlled composition and thermo-mechanical processing to achieve an optimal strength-ductility balance. Full article

Background: gemcitabine is a cytidine analog and major anticancer drug functioning as an antimetabolite. However, its administration by systemic route is accompanied by “burst” and side effects. To limit this, drugs are encapsulated in matrices; metal–organic frameworks (MOFs) are coordination polymers with strong potential for drug encapsulation and delayed release. Methods: mechano-chemical synthesis of solid-state binary complex lag(CYCU-3)(Gem) is described from aluminum MOF (Al-MOF) CYCU-3 and gemcitabine free base (Gem). Synthesis is conducted by liquid-assisted grinding (LAG) with dimethyl sulfoxide (DMSO) followed by its outgassing. The alternative “dry” synthesis results in dry(CYCU-3)(Gem). Materials were characterized by FTIR spectroscopy and XRD, and delayed Gem release was tested to phosphate buffered saline (PBS) at 37 °C. The in vitro toxicity to pancreatic cancer PANC−1 and healthy cells hTERT−HPNE E6/E7/K−RasG12D was assessed by fluorometric assay. Results: in lag(CYCU-3)(Gem) interactions MOF-drug are via non-covalent bonds at O-H and COO⁻ groups of CYCU-3 as found by FTIR marker peak shifts and crystal structure is retained, while dry(CYCU-3)(Gem) shows significant amorphization and loss of functional groups. The lag(CYCU-3)(Gem) but not dry(CYCU-3)(Gem) shows delayed Gem release for 6000 min. The suppression of PANC−1 cells by lag(CYCU-3)(Gem) is time-dependent and it correlates with delayed Gem release. For the first time, a concept of ternary stoichiometric complex lag(CYCU-3)₁(Gem)₁(CIT)₂ is tested that also contains natural organic compound citronellol (CIT), and its structure, bonding and release of Gem are compared to those of binary complex. Bonding is at the O-H groups of CYCU-3 and this complex shows delayed Gem release. Conclusions: binary and ternary complexes of Gem with CYCU-3 yield delayed release and cytotoxicity. LAG is promising for synthesis of solid-state complexes of gemcitabine for delayed release and time-dependent suppression of cancer cells. Full article