Continued corrosion protection of aluminium alloy 2024 through layered double hydroxide UV-degradation

ABSTRACT: In the last decade, the necessity to improve corrosion protection has dramatically affected the industry. Layered double hydroxides emerge as a possibility to overcome this problem due to their ability as a carrier of corrosion protection species. In this work, cerium cations, which possess corrosion protection ability, were incorporated in the LDH structure via partial substitution of aluminium cations. The changes occurring to LDH when exposed for an extended period to UV-radiation and its degradation with release of Ce3+ from the hydroxide layers has been studied and is presented in this work.info:eu-repo/semantics/publishedVersio

Investigation of ferroelectric behavior of Bi(Fe,Sc)O3 multiferroics using piezoresponse force microscopy

This work was supported by the TUMOCS project that has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No 645660

Faraday effect and fragmentation of ferromagnetic layers in multilayer Co/Cu(1 1 1) nanofilms

With purpose to investigate influence of magnetically non-active metal layers on the Faraday effect in multilayer Ferromagnetic/Normal metal films, dependences of the Faraday rotation angles of the light polarization plane on magnetic field have been studied in multilayer [Co/Cu] nanofilms. It was revealed that the Faraday rotation φ varies with thickness of the Cu layers dCu. This φ(dCu) dependence consists of the monotonic component, namely a gradual rise of the angle with increase of dCu, and the non-monotonic one represented by two minima. The monotonic changes of the Faraday rotation were satisfactory described in frames of the effective medium method. Two minima are explained with the Co layer’s fragmentation due to influence of size electron quantization in the Cu layers on formation of Co clusters during deposition of the films.publishe

Sol-gel synthesis and characterization of non-substituted and europium- substituted layered double hydroxides Mg3/Al1-xEux

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Exchange bias phenomenon in (Nd1-xYx)2/3Ca1/3MnO3 (x = 0, 0.1) perovskites

Exchange bias phenomenon, evident of antiferromagnetic-ferromagnetic phase segregation state, has been observed in (Nd1-xYx)2/3Ca1/3MnO3 (x = 0, 0.1) compounds at low temperatures. A contribution to the total magnetization of the compounds due to the ferromagnetic phase has been evaluated. It has been found that yttrium doping leads to the growth of the ferromagnetic phase fraction. The ferromagnetic phase in the doped compound has a lower coercivity Hc and more rectangular form of the hysteresis loop. The values of the exchange bias field HEB and coercivity are found to be strongly dependent on the cooling magnetic field Hcool. In sufficiently high magnetic fields, Hcool > 5 kOe, HEB in the doped compound is about twice as low as in the parent compound. This difference is attributed to a lower exchange interaction and higher saturation magnetization of the ferromagnetic phase in (Nd0.9Y0.1)2/3Ca1/3MnO3

Cast iron corrosion protection with chemically modified Mg Al layered double hydroxides synthesized using a novel approach

Layered double hydroxides (LDHs) intercalated with corrosion inhibitive species are considered as promising additives to protection coatings. However, the conventional method of LDH preparation via co-precipitation followed by anion exchange is a water consuming and slow process hardly applicable to industrial use. In this work, a novel approach to LDH synthesis via hydration of sol-gel prepared mixed metal oxides and two-step anion exchange, all assisted by high-power sonication, was applied. Mg—Al and Mg-Al-Ce LDH with cations ratios 2:1 and 2:0.9:0.1, respectively, intercalated with corrosion inhibitive dihydrogen phosphate anion were successfully prepared. The obtained LDH were characterized by X-ray diffraction and scanning transmission electron microscopy. Anion release from these LDH in NaCl solutions and their corrosion inhibitive action on cast iron samples were monitored by electrochemical impedance spectroscopy. The results show that the dihydrogen-phosphate-intercalated LDHs produced using the novel technique are efficient in corrosion protection.publishe

Exchange bias effect in bulk multiferroic BiFe0.5Sc0.5O3

Below the Néel temperature, TN ∼ 220 K, at least two nano-scale antiferromagnetic (AFM) phases coexist in the polar polymorph of the BiFe0.5Sc0.5O3 perovskite; one of these phases is a weak ferromagnetic. Non-uniform structure distortions induced by high-pressure synthesis lead to competing AFM orders and a nano-scale spontaneous magnetic phase separated state of the compound. Interface exchange coupling between the AFM domains and the weak ferromagnetic domains causes unidirectional anisotropy of magnetization, resulting in the exchange bias (EB) effect. The EB field, HEB, and the coercive field strongly depend on temperature and the strength of the cooling magnetic field. HEB increases with an increase in the cooling magnetic field and reaches a maximum value of about 1 kOe at 5 K. The exchange field vanishes above TN with the disappearance of long-range magnetic ordering. The effect is promising for applications in electronics as it is large enough and as it is tunable by temperature and the magnetic field applied during cooling.publishe

Multiferroic Bi 0.65 La 0.35 Fe 0.5 Sc 0.5 O 3 perovskite:Magnetic and thermodynamic properties

Magnetic and thermodynamic properties of polycrystalline multiferroic Bi 0.65 La 0.35 Fe 0.5 Sc 0.5 O 3 synthesized under high-pressure and high-temperature conditions are reported. Magnetic properties were studied using a SQUID magnetometer technique over the temperature range of 5−300 K in magnetic fields up to H=10 kOe. The field dependent magnetization M(H) was measured in magnetic fields up to 50 kOe at different temperatures up to 230 K after zero-field cooling procedure. A long-range magnetic ordering of the AFM type with a weak FM contribution occurs below the Néel temperature T N ~237 K. Magnetic hysteresis loops taken below T N show a huge coercive field up to H c ~10 kOe. A strong effect of magnetic field on the magnetic properties of the compound has been found. Derivative of the initial magnetization curves demonstrates a temperature-dependent anomaly in fields of H=15−25 kOe. Besides, an anomaly of the temperature dependent zero-field cooled magnetization measured in magnetic fields of 6−7 kOe has been found. Origin of both anomalies is associated with inhomogeneous magnetic state of the compound. The heat capacity has been measured from 2 K up to room temperature and a significant contribution from the magnon excitations at low temperatures has been detected. From the low-temperature heat capacity, an anisotropy gap of the magnon modes of the order 3.7 meV and Debye temperature T D =189 K have been determined

Phase formation in the (1- y )BiFeO 3 - y BiScO 3 system under ambient and high pressure

Formation and thermal stability of perovskite phases in the BiFe1-yScyO3 system (0≤y≤0.70) were studied. When the iron-to-scandium substitution rate does not exceed about 15 at%, the single-phase perovskite ceramics with the rhombohedral R3c symmetry (as that of the parent compound, BiFeO3) can be prepared from the stoichiometric mixture of the respective oxides at ambient pressure. Thermal treatment of the oxide mixtures with a higher content of scandium results in formation of two main phases, namely a BiFeO3-like R3c phase and a cubic (I23) sillenite-type phase based on γ-Bi2O3. Single-phase perovskite ceramics of the BiFe1-yScyO3 composition were synthesized under high pressure from the thermally treated oxide mixtures. When y is between 0 and 0.25 the high-pressure prepared phase is the rhombohedral R3c with the √2ap×√2ap×2√3ap superstructure (ap ~ 4 Å is the pseudocubic perovskite unit-cell parameter). The orthorhombic Pnma phase (√2ap×4ap×2√2ap) was obtained in the range of 0.30≤y≤0.60, while the monoclinic C2/c phase (√6ap×√2ap×√6ap) is formed when y=0.70. The normalized unit-cell volume drops at the crossover from the rhombohedral to the orthorhombic composition range. The perovskite BiFe1-yScyO3 phases prepared under high pressure are metastable regardless of their symmetry. At ambient pressure, the phases with the compositions in the ranges of 0.20≤y≤0.25, 0.30≤y<0.50 and 0.50≤y≤0.70 start to decompose above 970, 920 and 870 K, respectivelypublishe

Review: Effects of Ractopamine Hydrochloride (Paylean) on welfare indicators for market weight pigs

This review summarizes the effects of ractopamine hydrochloride (RAC) dose (5, 7.5, 10, and 20 mg/kg) on market weight pig welfare indicators. Ractopamine hydrochloride (trade name Paylean) is a β-adrenergic agonist that was initially approved in the U.S. in 1999 at doses of 5 to 20 mg/kg to improve feed efficiency and carcass leanness. However, anecdotal reports suggested that RAC increased the rate of non-ambulatory (fatigued and injured) pigs at U.S. packing plants. This led to the addition of a caution statement to the Paylean label, and a series of research studies investigating the effects of RAC on pig welfare. Early research indicated that: (1) regardless of RAC administration, fatigued (non-ambulatory, non-injured) pigs are in a state of metabolic acidosis; (2) aggressive handling increases stress responsiveness at 20 mg/kg RAC, while 5 mg/kg reduces stress responsiveness to aggressive handling. Given this information, dosage range for Paylean was changed in 2006 to 5 to 10 mg/kg in market weight pigs. Subsequent research on RAC demonstrated that: (1) RAC has minimal effects on mortality, lameness, and home pen behavior; (2) RAC fed pigs demonstrated inconsistent prevalence and intensity of aggressive behaviors; (3) RAC fed pigs may be more difficult to handle at doses above 5 mg/kg; and (4) RAC fed pigs may have increased stress responsiveness and higher rates of non-ambulatory pigs when subjected to aggressive handling, especially when 20 mg/kg of RAC is fed