Formation Of Layer Research Articles

Anti-Corrosion Performance of Magnesium Potassium Phosphate Cement Coating on Steel Reinforcement: The Effect of Boric Acid.

It has recently been found that magnesium potassium phosphate cement (MKPC) paste coating applied on the surface of steel reinforcement can effectively retard the onset of corrosion and suppress corrosion reactions. However, the fast-setting nature of MKPC-which is a merit in repair-can be problematic in a practical engineering process of coating the steel reinforcement with MKPC paste. To address this problem, boric acid (H3BO3) was added as a retarder in an MKPC formulation to prolong the setting time. This work investigated the impact of boric acid (at 5% by weight of MgO) on the anti-corrosion performance of MKPC paste coating through a series of electrochemical (EC) tests. The results showed that the anti-corrosion performance of MKPC paste coating for a mild steel bar could be interfered with by the presence of boric acid. In the same testing situation (immersed in 3.5 wt.% NaCl corrosion solution), the polarization resistance and corrosion current density of the group including boric acid were inferior and exceeded the corrosion thresholds prior to the control group without boric acid. Meanwhile, the time constant phase in the frequency range from 1 Hz to 10 kHz was rarely observed, implying that the presence of boric acid probably impaired the formation of the passivation layer. This decrease in anti-corrosion performance of MKPC paste coating could be related to the larger volume fraction of pores in the range from 0.1 to 10 µm that are formed during the initial stage of coating formation.

Adsorption removal of copper(II) from water by zero valent iron loaded dendritic mesoporous silica

The object of research is synthesized dendritic mesoporous nanoscale silica (DMSN) modified with zero-valent iron (Fe0@DMSN). This material exhibits a high adsorption capacity for heavy metal ions, in particular copper, whose increased content in the aquatic environment poses a threat to living organisms. In this regard, the main physicochemical features of the removal of copper cations from the aqueous medium using the obtained sample were investigated. The morphology of the obtained dendritic silicas was studied by electron microscopy and the presence of a layer of zero-valent iron was confirmed by X-ray diffraction analysis and infrared spectroscopy. The parameters of the porous structure of the synthesized materials were determined. It was found that after modification of mesoporous silica with particles of zero-valent iron, the value of its specific surface area decreased from 504 m2/g to 312 m2/g. This may be due to the formation of a Fe0 layer not only on their surface but also in the channels of the inorganic matrix, which has a unique dendritic structure characteristic of this type of particles. At the same time, the number of active centers increases due to the enrichment of the silica surface with functional modifier groups that show a high affinity for metal cations. The adsorption capacity of Fe0@DMSN towards Cu2+ ions has been studied and it has been shown that the maximum adsorption value is 39.8 mg/g, which is significantly higher than that of the initial synthesized DMSN sample (0.7 mg/g). The experimental data obtained indicate that the obtained sorption material based on dendritic mesoporous silica nanoparticles with a layer of reactive zero-valent iron can be used for the purification of water contaminated with metal ions. In addition, the magnetic properties of such materials, known and proven by various scientists, will make it easy to separate the solid phase in the processes of sorption water purification using magnetic separation.

Effect of Alkaline Etching on Formation Behavior and Corrosion Resistance of a Cr-Zr-Ti TCP Conversion Coating on AA2024 Aluminum Alloy

Abstract Trivalent chromium process conversion coating is considered to be the ideal alternative to traditional chromate conversion coating due to its high corrosion resistance and low toxicity. However, achieving a high corrosion resistance trivalent chromium conversion coating on 2xxx aluminum alloys has been a great challenge. Herein, based on a newly developed trivalent chromium conversion solution (CN patent, ZL 202210804263.2), the effect of alkaline etching on the formation behavior and corrosion resistance of the coating on AA2024-T351 aluminum alloy was investigated. It was found that under the same conditions, the mechanically polished sample and the sample alkaline etched for 30 s showed the highest corrosion resistance. When the alkaline etching time was too short or too long, the corrosion resistance of the coating deteriorated. This is ascribed to changes in the surface microstructure of the alloy during alkaline etching, i.e., reduced number of intermetallic particles and formation of a copper enrichment layer. Reducing the number of intermetallic particles on the alloy surface is beneficial for uniform growth of the coating. However, the copper enrichment layer participated in formation of the coating, resulting in doping of copper species in the coating, which is detrimental to the corrosion resistance of the coating.

Photoluminescence of Tetra(benzimidazole)phenylethene Derivatives and Their Carbene Metallacycles in Aggregates and Langmuir-Blodgett Films.

Molecular structure, external stimuli, and environmental factors all have a strong effect on the internal molecular rotation and vibration of aggregate-induced emission (AIE) luminogens. Here, we report the AIE effect for several newly synthesized amphiphilic tetra(benzimidazole)phenylethene (TBiPE) derivatives and their binuclear N-heterocyclic carbene silver (NHC-Ag) metallacycles in solutions, aggregates, and Langmuir-Blodgett (LB) films. Monolayer behaviors and microscopic images indicate that introducing alkyl chains and binuclear NHC-Ag metallacycles can facilitate the formation of a well-defined insoluble monomolecular layer at the air-water interface. Absorption and luminescence spectral features suggest that both the TBiPEs' cyclization structure and binuclear NHC-Ag metallacycles can provide additional driving forces to restrict the internal molecular motion of the tetraphenylethene (TPE) unit, thus enhancing the AIE effects. Further, external stimuli and environmental factors such as poor solvent addition and LB film deposition also play important roles in the photoluminescent intensity, maximum wavelength, and lifetime. These internal and external factors can result in around 30-40 nm blue-shift for the maximum luminescence wavelength and 2-3 times shorter for the luminescent lifetime. These phenomena can be attributed to the reason that the nonradiative energy transfer efficiency is weakened because of the enhanced hydrophobic interaction and metal-carbene coordination as well as the closely packed arrangement of AIEgens in the LB films; consequently, the radiation energy transfer efficiency increased.

Effects of manganese and copper co-doped bioactive glasses with photothermal response on osseous cells

Herein, a series of bioactive glasses with a composition based on SiO2Na2OCaO-P2O5-Bi2O3, doped with either manganese (Mn) or copper (Cu), or a combination of both have been developed. The aim was to create a biocompatible, bioactive material with a photothermal (PT) response for potential use in bone cancer treatment. UV/vis/NIR spectroscopy indicated that the addition of Cu to the glass resulted in a broadband absorption of around 800 nm, while Mn showed an absorption band of around 500 nm. Photoluminescence (PL) spectroscopy, which was performed by exciting the specimen using a 750 nm beam, revealed an emission at 823 nm for all glass compositions, but with varying intensities. When exposed to an 808 nm laser (5 W/cm2), the glass samples exhibited temperature rising, with the sample containing both Mn and Cu, showing the highest absorption peak, reaching 204 °C after 5 min. The degradation rate of the glass in a phosphate-buffered saline (PBS) solution was influenced by the presence of Mn and Cu. Cytotoxic assessment on osteoblast-like cells showed that the presence of Mn promoted cell proliferation by over 20 % after 24 h, but when irradiated with an 808 nm laser, the viability of cells decreased by nearly 60 % due to heat ablation. Finally, the glass sample demonstrated in vitro bioactivity through the formation of a hydroxyapatite layer on its surface when immersed in simulated body fluid.

Impact of Electrolyte Additives on the Lifetime of High Voltage NMC Lithium-Ion Pouch Cells

Abstract This work involves improving the lifetime of lithium-ion cells during high voltage cycling using electrolyte additives. Three generations of electrolyte additives were investigated and screened in NMC442/graphite pouch cells using a 24 h voltage-hold protocol at 40°C to accelerate oxidative reactions occurring at 4.4 V. Once promising additives and combinations were identified, they were then tested in cobalt-free NMC640/graphite cells for long-term cycling to upper cutoff voltages of 4.3, 4.4, and 4.5 V at temperatures of 20, 40, and 55°C. Degradation mechanisms were probed using dV/dQ analysis, micro-X-ray fluorescence spectroscopy, and electrochemical impedance spectroscopy. The primary failure mode of cells held at high voltages is due to increase in cell impedance, which is correlated to the dissolution of transition metals, specifically manganese, originating from the positive electrode. We believe this dissolution is presumably due to the formation of a high impedance rock salt surface layer on the NMC positive electrode particles. Such deleterious outcomes can be limited by selecting an appropriate electrolyte additive package. It is hoped that this paper can provide a starting point for developing NMC Li-ion cells that can operate to voltages as high as 4.4 V and still display long lifetimes.

Data-driven AI for the automated classification of the isothermal heat-treated thermal barrier coatings using pulsed infrared thermography

Abstract Thermal barrier coating (TBC) is a multilayer coating applied to metallic structures exposed to high temperatures, such as aero-engine parts and gas turbine blades. These thermally insulating materials are used to extend the component life by minimizing the high-temperature exposure of structural components. As a result of the high-temperature oxidation tests, a thermally grown oxide (TGO) layer formed at the interface between the ceramic topcoat layer and the bond coat layer. The primary cause of TBC performance decline and structure failure is the growth of the oxide layer. Hence, it is crucial to regularly monitor the formation of the oxide layer and the degradation of coatings. This can be achieved by developing coating-life prediction models, which are vital for quality control, health monitoring of TBCs, maintenance decision-making, and the prevention of catastrophic failures. Existing methods for life estimation, which are dependent on empirical methods and microstructural analysis, often fail due to various material compositions and service conditions. This study proposes an automated classification of iso-thermal heat-treated TBC samples using temperature data, which helps in predicting the TBC life and monitoring the TBC degradation. TBC-coated samples are isothermal heat-treated at 1000 °C, and the initial growth of TGO is monitored using a non-destructive thermal imaging technique. Identifying distinctive features in each class corresponding to layer thickness measurement and service hours is challenging and time-consuming. So, we integrate data-driven AI models and feature extraction techniques to interpret complex thermal patterns. The performance of deep learning models and classical machine learning models demonstrates that our method can achieve maximum classification accuracy and F1-score of 89.2% and 89.0%, respectively. This automated classification framework promises a powerful tool for predictive maintenance and remaining useful lifetime estimation of hot section components reliant on TBCs.

Microporous Polyethylene and Cellulose Composite Separators for Reversible Lithium Electrode in Lithium Rechargeable Batteries

AbstractThe lithium metal anode is the best candidate for high energy density batteries because of its high specific capacity and low negative potential. Rechargeable lithium metal batteries (RLMB) have not yet been commercialized. The key factors that limit the practical use of RLMB are the formation and growth of lithium dendrites during the lithium deposition process and the reaction of the lithium anode with the organic solvent of the electrolyte, quantified by the Columbic efficiency (CE). To suppress the lithium dendrite formation and to improve CE, many approaches such as the formation of a protective layer on the lithium electrode and the use of additives to the electrolyte have been proposed. In this study, the effect of a thin cellulose film to improve CE of lithium deposition and stripping on the lithium electrode was examined. The cycle performance of a Li/Li symmetrical cell with a cellulose and polyethylene composite separator was examined for a carbonate electrolyte and an ether electrolyte. The improvements of CE were observed for both electrolytes with the cellulose film separator. The improvement could be explained by the good wettability of the cellulose film separator with the electrolyte.

Corrosion Inhibition and Adsorption Behaviour of Centrosema pubescens Leaf Extract for Copper in HCl Solution

Study’s Excerpt In this study, Centrosema pubescens leaf extract (CPE) has been confirmed as eco-friendly and efficient green inhibitor for copper corrosion in hydrochloric acid. Detailed thermodynamic analysis, revealed that CPE adsorption follows a Freundlich isotherm model. SEM-EDX and FTIR characterizations confirmed the formation of a protective layer confirming the potentials of the plant extracts in sustainable corrosion prevention. Full Abstract The anti-corrosion behaviour of Centrosema pubescens leaf extract (CPE) on copper in 1.5 M hydrochloric acid was investigated using weight loss method at different temperatures, followed with scanning electron microscopy (SEM) surface characterization connected with energy dispersive X-ray spectroscopy (EDX). The Fourier transform infrared spectrum of CPE was obtained. CPE inhibition effectiveness depends on the temperature and its concentration. CPE restrains the copper corrosion with 94.26 % inhibition efficiency at 1.0 g/L of CPE and at 303 K. For the CPE-inhibited system, a higher activation energy (Ea) value (range of 31.09 to 38.70 kJmol-1) compared to 20.34 kJmol-1 of the blank solution was obtained. The reaction process is spontaneous and endo thermic, as indicated by the ΔH, ΔS and ΔG values calculated. CPE adsorption behaviour fitted best into Freundlich isotherm.

Synthesis and Electrochemical Properties of Oleylamine as a Sour Saline Corrosion Inhibitor Under Laminar Flow at 40 °C.

In this study, the synthesis of a long-chain aliphatic amino compound and its sour corrosion inhibition properties were reported. Oleylamine was obtained through the reaction of 4-(Aminomethyl) pyridine with 1-chloro-octadecane. The identification and characterization of reaction products were carried out through Fourier transform infrared spectroscopy (FTIR) and gas chromatography/mass spectroscopy (GC-MS). Oleylamine was tested as a sour corrosion inhibitor for steels. Different concentrations of oleylamine (0, 5, 10, 25, and 100 ppm) in a sour saline electrolyte were analyzed. The dynamic anticorrosive behavior of oleylamine on carbon mild steel (AISI 1018) surfaces was evaluated using a laminar flow of 100 rpm and tested with potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS) measurements. After electrochemical testing, the surface of the steel specimens that were used was characterized with Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The electrochemical results of the anticorrosive efficiency of oleylamine for steel showed an exponential behavior as a function of inhibitor concentration. At a concentration of 20 ppm of the inhibitor, the anticorrosive efficiency did not show any significant changes. However, at 100 ppm of the inhibitor, an efficiency of over 95% was achieved. After the electrochemical tests, the surface of the steel samples with the inhibitor revealed the formation of an inhibitor layer that prevented the corrosion of the steel.

Study on the mechanical properties of PES-HmA samples printed by selective laser sintering under various pre-heating conditions

The purpose of this study is to investigate the influence of pre-heating characteristics on the mechanical properties and forming process of selective laser sintering (SLS) printed PES-HmA samples. An experimental setup with four heating tubes was designed to study the pre-heating temperature distribution on the powder bed. The pre-heating temperature distribution on the powder bed was captured using a thermal imaging camera. A method for evaluating pre-heating temperature distribution based on the average and standard deviation of surface temperature was proposed. The heating tube installation position was optimized using a response surface experiment study based on the temperature distribution evaluation. By optimizing the installation position of the tubes, the temperature distribution on the powder bed tends to become uniform. The effect of pre-heating temperature value and distribution on the mechanical properties of the SLS printed PES-HmA samples was also experimentally investigated. The cross sectional microstructure of the printed samples were examined by scanning electron microscope to analyze the layer formation process at different pre-heating temperature. By increasing the pre-heating temperature from 70°C to 100°C, the material diffusion at the layers interface was improved, which made the tensile strength of sample increased by 376%, and the flexural strength increased by 224%.

Local Delivery of Exosomes and Antibiotics in Hydroxyapatite-Based Nanocement for Osteomyelitis Management.

The management of bone and joint infections is a formidable challenge in orthopedics and poses a global health concern. While clinical management emphasizes infection prevention and complete eradication, an effective strategy for stabilizing skeletal tissue with adequate soft tissue coverage remains limited. In this study, we have employed a novel approach of using the local delivery of exosomes and antibiotics (rifampicin) using a hydroxyapatite-based nanocement carrier to manage the residual space created during debridement effectively. Additionally, we synthesized a periosteum-guiding antioxidant herbal membrane to leverage the inherent periosteum regeneration capability of the bone, facilitating bone callus repair and natural healing. The synthesized scaffolds were biocompatible and demonstrated potent antibacterial activity in vitro. When evaluated in vivo in the Staphylococcus aureus-induced rat tibial osteomyelitis model, the released drugs successfully cleared the residual bacteria and the released exosome promoted bone healing, resulting in 3-fold increase in bone volume as analyzed via micro-CT analysis. Immunofluorescence staining of periosteum-specific markers also indicated the complete formation of periosteal layers, thus highlighting the complete bone repair.

Reactive Spark Plasma Sintering and Oxidation of ZrB2-SiC and ZrB2-HfB2-SiC Ceramic Materials

This study presents the fabrication possibilities of ultra-high-temperature ceramics of ZrB2-30 vol.%SiC and (ZrB2-HfB2)-30 vol.% SiC composition using the reaction spark plasma sintering of composite powders ZrB2(HfB2)-(SiO2-C) under two-stage heating conditions. The phase composition and microstructure of the obtained ceramic materials have been subjected to detailed analysis, their electrical conductivity has been evaluated using the four-contact method, and the electron work function has been determined using Kelvin probe force microscopy. The thermal analysis in the air, as well as the calcination of the samples at temperatures of 800, 1000, and 1200 °C in the air, demonstrated a comparable behavior of the materials in general. However, based on the XRD data and mapping of the distribution of elements on the oxidized surface (EDX), a slightly higher oxidation resistance of the ceramics (ZrB2-HfB2)-30 vol.% SiC was observed. The I-V curves of the sample surfaces recorded with atomic force microscopy demonstrated that following oxidation in the air at 1200 °C, the surfaces of the materials exhibited a marked reduction in current conductivity due to the formation of a dielectric layer. However, data obtained from Kelvin probe force microscopy indicated that (ZrB2-HfB2)-30 vol.% SiC ceramics also demonstrated enhanced resistance to oxidation.

Sustainable Grease Lubrication Induced by Graphene Oxide and LiFePO4

This study investigates the possibility of modifying lubricating greases by 2D graphene oxide (GO) and lithium iron phosphate (LiFePO4) to enhance their tribological performance. GO's layered structure plays a crucial role in reducing friction by facilitating easy sliding between rubbing surfaces, making it an effective solid lubricant. The impact of these additives on friction reduction, wear resistance, and the tribolayer formation ability is evaluated by ball‐on‐disc tribometry with an emphasis on durability and sustainability. Comparative results reveal that unmodified greases exhibit a high susceptibility to wear, including oxide formation and severe plastic deformation. In contrast, greases with GO show a notable reduction in friction, while the addition of LiFePO4 contributes to the formation of a continuous protective layer that substantially reduces abrasive wear. The combination of GO and LiFePO4 results in a homogeneous, durable tribofilm that effectively protects surfaces against severe wear providing long‐term friction stability. Although lab‐scale LiFePO4 is used, the findings suggest a great potential for extending the useful life of recycled LiFePO4 from lithium‐ion batteries, similar to commercial LiFePO4 thus confirming significant improvements in the grease performance but also highlighting the potential to advance toward more sustainable solutions in industrial applications and electric vehicles.

Corrosion studies of Al-Mg-Sc-Zr Alloy with Low Sc/Zr ratio fabricated by laser powder bed fusion for marine environments

This study investigates the corrosion behavior of a laser powder bed fusion (LPBF) Al-Mg-Sc-Zr alloy with a Sc/Zr ratio of less than 1 in 3.5wt% NaCl solution. X-ray diffraction (XRD) analysis revealed the presence of an Al matrix with face-centered cubic (FCC) structure and the secondary phase Al3(Sc,Zr) with L12 crystal structure. Microstructural analysis indicated a bimodal grain size distribution with fine equiaxed and columnar grains influenced by thermal gradients and secondary phase Al3(Sc,Zr). Potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) tests in 3.5wt% NaCl solution demonstrated that the alloy exhibits a less negative corrosion potential (Ecorr) and lower corrosion current density (icorr) compared to other Al-Mg-Sc-Zr alloys with higher Sc/Zr ratios, indicating superior corrosion resistance. The enhanced performance is attributed to the fine grain structure and the formation of a stable protective oxide layer facilitated by the higher Zr content.

Comprehensive characterizations of core sediments recovered from Shenhu W17 well in South China sea and its impact on methane hydrate kinetics

Natural Gas Hydrates (NGH) is considered a vast unconventional energy source that holds significant promise in addressing future energy demands. In Shenhu area (located at northern slope of the South China Sea, SCS), there has been conducted a series of further studies of NGH such as exploration, drilling, and twice field production testing. The lithological characteristics of cores from marine sediments and their influence on methane hydrate (MH) formation are relatively unknown and merits further investigation. In this study, we conducted a chain of lithological characterization on the core sediments recovered from Shenhu W17 well, the coring well which located near the 1st NGH field production in SCS. The core sediments are classified as clayey-silt, its median grain size is 6.91 μm, comprising primarily clay minerals, quartz, and calcite. According to X-ray diffraction analysis, the main content of clay minerals is illite-smectite layers, illite, chlorite, and kaolinite, respectively. Porosity of the core sediments is 32.5% and the permeability is 7.8 mD based on mercury intrusion tests. Four types of primary pores are identified based on SEM and QEMSCAN analysis: intergranular pore, intercrystalline pore, intragranular pore, and pores associated with marine fossils. Moreover, the influence of the recovered core sediments (0–40 wt%) on MH formation kinetics were examined with morphology observed to elucidate the MH-core sediments interaction. The induction time was reduced significantly to ∼20 min in the presence of SCS core sediments. A two-stage MH formation behavior is observed with a maximum gas uptake of 134.1 Vg·Vw−1: (a) an initial MH formation at the gas-liquid interface with MH upward growth and fine-grain sediments migration; and (b) a second stage of significant MH growth with layered formation of MH and core sediments. The capillary channels of MH formed facilities the migration of core sediments, which in turn provides additional gas-liquid contact area for MH formation. The study provides valuable insights on the role Shenhu core sediments in MH formation, which is essential for understanding the spatial heterogeneity of NGH in reservoir and for designing suitable production strategy.

Effects of graphene content on formation and characteristics of char layer in intumescent coating

This study provides a better understanding of the role and mechanism of graphene nano-platelets used as a flame-retardant filler in a commercial intumescent acrylic-based formulation. Through thermogravimetric analysis, the morphology and mechanical properties of the char layer as well as the influence of graphene on the expansion ratio and compression force are clarified. The achieved results demonstrate that graphene accelerates the burning of the coating and affects the structure of the char layer. The fire test was carried out in an electric furnace at a temperature of up to 800 °C for our fabricated samples, the swelling images show that the expansion ratio of the graphene-loaded coating is lower than that of the coating without graphene. On the other hand, during the combustion, the speed of air release occurring in a short time also contributes to forming bigger holes in the char layer, so the hardness of the graphene-loaded char layer is lower than that of the char layer without graphene coating.

Enhanced signal to noise ratio of single entity electrochemistry signal of platinum nanoparticles using passive silver ultramicroelectrode

AbstractThe single‐entity electrochemistry (SEE) of electrocatalytic platinum (Pt) single nanoparticles (NPs) on a less electrocatalytic silver (Ag) ultramicroelectrode (UME) surface was investigated using the electrocatalytic amplification method. Two characteristic types of current responses—current staircases and blips (or spikes)—were observed during single NP collision experiments, depending on the applied potential at the Ag UME. Notably, at applied potentials of 0.13 and 0.17 V, the Ag UME becomes passive due to the formation of a delicate oxide layer, resulting in a highly stable background current. This leads to an enhanced signal‐to‐noise (S/N) ratio, attributed to the low background current, when using Ag UME compared to commonly used UMEs such as Au, C, Ni, and Hg for the SEE of Pt NPs. The exceptionally low background current can provide a significant advantage for detailed observation of SEE signals and further mechanistic studies based on the current response.

Preparation of a polyurethane‐coated expandable graphite and its flame retardant application in rigid polyurethane foams

AbstractExpandable graphite (EG) is widely used in rigid polyurethane (PU) foam (RPUF) as flame retardant, however, the mechanical properties of RPUF would deteriorate with the increase of its content. To alleviate this problem, PU‐coated EG (PUEG) is prepared by coating PU on the surface of EG via interface polymerization. PUEG is characterized by FTIR, XPS, and SEM. The results show that PUEG is successfully prepared. Compared with the RPUF add with the pure EG, the compressive strength and flame retardancy of the RPUF prepared by adding 15% PUEG have been improved to varying degrees. A 15% PUEG and 20% PUEG modify RPUFs obtained both UL‐94 V‐0 rating with LOI values of 29.7% and 31.2%, respectively. The improvement in the flame retardancy and compressive strength of RPUF is due to the good interfacial compatibility between the RPUF and PU on the surface of the EG and the increased coking rate of the EG, which accelerates the formation of the thermal barrier carbon layer. The preparation process of PUEG is simple and suitable for large‐scale production.

Antagonistic CLE peptide pathways shape root meristem tissue patterning.

Secreted CLAVATA3/EMBRYO SURROUNDING REGION (CLE) peptide ligands dimension the stem cell niche of Arabidopsis shoot meristems by signalling through redundant and cross-compensating CLAVATA1 (CLV1)-type receptor kinases. In the root meristem, the CLV1 homologues BARELY ANY MERISTEM 1 (BAM1) and BAM2 drive CLE13/16-mediated formative divisions that produce the ground tissue layers. Here we report that BAM1/2 are also required to initiate the vascular phloem lineage and that cross-compensation between CLV1-type receptors as observed in the shoot does not operate similarly in the root. Rather, we find that BAM3-mediated CLE45 signalling antagonizes BAM1/2-mediated CLE11/12/13 signalling in the phloem initials but not in the ground tissue. We further observe spatiotemporally contrasting CLE signalling requirements for phloem initiation and differentiation, which are shaped by the SHORT ROOT (SHR) pathway. Our findings thus suggest an intricate quantitative interplay between distinct and antagonistic CLE signalling pathways that organizes tissue layer formation in the Arabidopsis root meristem.