Twelve nontronites and two ferruginous smectites have been characterized with respect to Fe3+ occupancy of tetrahedral sites. The techniques used were near infrared, Fe-K X-ray absorption near-edge and X-ray absorption fine-structure spectroscopies, along with two X-ray diffraction techniques. The results show that calculations of the structural formulae of many nontronites should be adjusted to include Fe3+ in tetrahedral sites. The nontronite from Spokane County, Washington, (∼44% Fe2O3) is essentially an end-member with its non-siliceous tetrahedral sites occupied by Fe3+. Samples with chemical compositions similar to Garfield nontronite (∼36.5% Fe2O3) may have small amounts (<5% of total Fe3+) of tetrahedral Fe3+. Tetrahedral Fe3+ is unlikely to be present in samples containing less than ∼34% Fe2O3.

Two independent methods of crystal-size distribution analysis were compared: the Bertaut-Warren-Averbach XRD technique (MudMaster computer program) and high-resolution transmission electron microscopy (HRTEM). These techniques were used to measure thickness distributions of illite crystals (fundamental particles) from sets of illite-smectites from shales and bentonites that had expandabilities ranging from 86%S to 6%S. The illite-smectites were treated with a polymer (polyvinylopyrolidone, PVP) to separate them into fundamental particles for XRD and HRTEM investigations.

A systematic difference between XRD and HRTEM results was observed: XRD (area-weighted distributions) detected a larger fraction of thick (>4 nm) and a smaller fraction of thin crystals as compared to HRTEM (number-weighted distributions). As a result, XRD-determined distributions have larger mean thickness values and larger distribution parameters (α and β2). The measurements performed by the two techniques were verified by modeling XRD patterns of the PVP-illites, using the measured distributions as inputs. The modeling indicated that the XRD-determined distributions are very accurate. Selecting broader thickness distributions in MudMaster further improved the modeling results. The HRTEM measurements underestimate the proportion of coarse particles, in particular in shale samples, and this inaccuracy is attributed to the effect of using number-weighted (rather than area-weighted) distributions and to inaccurate counting statistics for thick crystals.

Much attention has been paid to the adsorption of Fe(II) onto mineral surfaces as it is a crucial step in enhancing the reductive activity of Fe(II) species. The present study elucidates the role of Fe(II) adsorbed on Fe (oxyhydr)oxides (γ-FeOOH, α-FeOOH, and α-Fe2O3) for the reductive transformation of 2-nitrophenol (2-NP), using cyclic voltammetry (CV). Studies of Fe(II) adsorption and 2-NP reduction kinetics showed that an increase in pH gave rise to an elevated density of adsorbed Fe(II) on mineral surfaces, which further resulted in an enhanced reaction rate of 2-NP reduction. In addition, CV tests showed that the enhanced activity of Fe(II) species is attributed to the negative shift of peak oxidation potential (EP) of the Fe(III)/Fe(II) couple. The dependence of adsorbed Fe(II) reactivity on pH values was proven by the three linear correlations obtained (ln k vs. pH, EPvs. pH, and ln k vs. EP). The present study demonstrated that the reductive activity of adsorbed Fe(II) species can be indicated by the EP value of active Fe(II) species. Moreover, the electrochemical approach can be used as an effective tool to study the reductive activity of adsorbed Fe(II) species in subsurface environments.

The supply of Corumbataí Formation rocks, which occur widely in the State of São Paulo, Brazil, and are used by Santa Gertrudes Ceramic Cluster, is dwindling and prospecting for new deposits is essential. The current study aimed to map and characterize new reserves of ceramic raw materials which would guarantee mineral and economic sustainability of the important concentration of ceramic-processing capability in that area, and thereby contribute to improving and diversifying the range of products manufactured and to promoting a greater presence in the international market. To achieve the proposed objectives, 16 profiles were sampled and the samples were submitted to granulometric analysis by laser diffraction, and the major elements by inductively coupled plasma-mass spectrometry, and the mineralogical compositions of clay samples were determined by X-ray diffraction and ceramic properties. Six lithofacies were identified and grouped into two facies associations: a lower shoreface association comprising massive siltstone (Sm) and laminated siltstone (Sl); lithofacies, and an upper shoreface association comprising heterolithic sandstone (Sh), lenticular sandstone (Sle), intercalated sandstone/siltstone (Si), and altered siltstone (Sa) lithofacies. The lithofacies of the lower shoreface association were more clayey, flux with a significant presence of illite and microcline, and a more uniform granulometry distribution, which made its classification possible, technologically, as stoneware and semi stoneware. The main application of this material is in the production of coatings through the wet milling process. The lithofacies of the upper shoreface association was sandier, had a refractory presence with kaolinite and montmorillonite, and had a less uniform granulometric distribution; technologically, it can be characterized as porous and semi-porous. The main application of this material is in the production of coatings by the dry milling process. The results obtained by facies analysis combined with the geochemical and ceramic properties of the Corumbataí Formation rocks revealed both vertical and lateral variations of the lithofacies, which influence their properties, behavior, and application as ceramic raw materials.

The use of microorganisms to remove Fe (oxyhydr)oxides from kaolins has the potential to be an effective method for upgrading the whiteness and brightness, and therefore the commercial value, of the kaolin. The purpose of the present study was to compare kaolin products obtained by currently used chemical leaching methods with a bioleaching treatment using Aspergillus niger in order to remove Fe from kaolin (from Canakkale, Turkey). The effects of pulp density, temperature, and oxalic acid concentration on the chemical leaching experiments were investigated using the ANOVA-Yates test. The greatest degree of removal of Fe from the kaolin sample (at 15% w/v pulp density, temperature of 80°C, oxalic acid concentration of 0.2 M, and a particle size of <63 µm) was found to be 94.89% in 120 min of leaching. The Fe content decreased from 1.723%) Fe2O3 to 0.088% Fe2O3. In a shake flask, bioleaching of kaolin by Aspergillus niger resulted in removal of 77.13% of the total Fe, suggesting that this strain is effective at removing Fe impurities from kaolin. The removal efficiency generally decreased with increased pulp density. The Fe content of the kaolin decreased from 1.723% Fe2O3 to 0.394% Fe2O3 (at 1% w/v pulp density, temperature of 25°C, Aspergillus niger 3 × 107 spores, and particle size of <63 µm) after 21 days of bioleaching.

Kaolinite is often a cause of deformation in soft-rock tunnel engineering, leading to safety problems. The mechanism of the deformation is closely related to the interaction between kaolinite and water molecules. Because kaolinite has multiple defects, the effects of Mg, Ca, and Fe(II) doping on the atomic structure of the kaolinite (001) surface, and the subsequent adsorption and penetration of H2O into the interlayer, were studied systematically using density-functional theory. The results showed that for the Mg-, Ca-, and Fe(II)-doped kaolinites (001), the surface relaxation around the doping layer changed from contraction to expansion, due to the redistribution of electrons. The adsorption energies of the H2O monomer on Mg-, Ca-, and Fe(II)-doped kaolinites (001) were less than on undoped kaolinite (001). The results further revealed that the H2O molecule can also adsorb on the hollow site on the second-layer O surface of the Mg-, Ca-, and Fe(II)-doped kaolinites (001). For the undoped kaolinite, however, the H2O molecule adsorbs on the surface only. The energetic barriers for penetration of H2O from the adsorption site on the surface to the adsorption site on the O surface of Mg-, Ca-, and Fe(II)-doped kaolinites were also calculated: 1.18 eV, 1.07 eV, and 1.41 eV, respectively. The results imply that the influences of Mg, Ca, and Fe(II) doping on kaolinite allow the adsorbed water molecules to penetrate from the on-surface adsorption site to the O-surface site.

The aim of this paper was to define the nature and the relative chronology of the diagenetic clay bearing assemblages within sandstones of the Middle Proterozoic Kombolgie formation (Northern Territory, Australia). The detrital minerals of these rocks comprise quartz, accessory zircon, tourmaline, rutile and rare phengitic white micas. Diagenetic features consist of pore-sealing secondary quartz overgrowths, strong compaction shown by interlocked structures and stylolith joints, local hematization and the occurrence of two distinct clay parageneses. Blocky crystals of dickite constitute the earlier diagenetic clays. Their FTIR spectra and their DTA curves, with a sharp dehydroxylation endothermic peak near 680°C, are characteristic of the well-ordered dickite already encountered in many deeply-buried sandstones. Quartz overgrowth may be contemporaneous with the crystallization of dickite. Illite occurred during a subsequent stage as grain coatings and as pseudomorphs of dickite in the residual pores of the sandstones. Illite seems to be contemporaneous with the major deformation features associated with compaction phenomena at the maximal burial conditions experienced by the sandstone formation. These illites are essentially of 2M1 polytype. They display pseudohexagonal platy crystals with average diameters ranging from 2 to 10 µm. Their chemical composition is Al-rich (Ca0.01Na0.02K1.72) ()(Si6.27IVAl1.73)O20(OH)4. These Proterozoic rocks provide a natural reference for the illite end-member occurring as a replacement of kaolin subgroup minerals during burial diagenesis of sandstones The textural properties of the Kombolgie sandstones (absence of fracture network, low porosity, well-developed macroscopic stylolith joints…) and the crystal structure of both the diagenetic dickite and illite would tend to indicate that the Kombolgie sandstones were buried at a depth exceeding 5 km.

Hydrothermal alteration led to development of the Yarıkçı clay deposit within the Mesozoic chlorite-, muscovite-, chlorite-muscovite-schist, and garnet-graphite phyllite units along NW–SE- and N–S-trending faults in Mihalıççık in western central Anatolia. The geological, mineralogical, and geochemical characteristics and genesis of this economically important clay deposit have not been examined in detail previously. The present study has attempted to fill this gap. Green smectitic and cream kaolinitic claystones are abundant with smaller amounts of gray illite, dark brown Fe oxides, and silica phases occurring as stockwork/fracture infill and stain/coating. These units are covered by a dark, hard, sharp-edged, and thick silica cap. Metamorphic units exhibit cataclastic texture due to tectonic activities. Muscovite is mostly degraded to kaolinite, and feldspars show sericitization and argillization. Kaolinite typically has a platy form with irregular margins and locally sub-rounded, book-like texture suggesting hydrolysis during the hydrothermal injections. The association of Fe oxides, cristobalite/tridymite/quartz, gypsum/anhydrite, and jarosite are indicative of intense hydrothermal activities and development of kaolinite under acidic geochemical conditions. The local enrichment of SiO2, Fe2O3, S, Cu, and Au also supports this suggestion. The leaching of Sr, Rb, Ba, and Zr, and the slight increase in LREE/MREE+HREE ratios together with the negative Eu and Ce anomalies suggest the selective dissolution of muscovite, garnet, feldspar, and pyroxene by the hydrothermal fluids. Thus, abundant claystones of smectite and kaolinite were formed via the increase in Al+Fe+Mg/Si and Al±Fe/Si ratios in the alkaline and acidic environment, respectively, under the tectonic control of hydrothermal activity as seen in the alteration of chlorite, muscovite, and feldspar in metamorphic units.

Shewanella putrefaciens CN32 reduces Fe(III) within two illites which have different properties: the Fithian bulk fraction and the <0.2 µm fraction of Muloorina. The Fithian illite contained 4.6% (w/w) total Fe, 81% of which was Fe(III). It was dominated by illite with some jarosite (∼32% of the total Fe(III)) and goethite (11% of the total Fe(III)). The Muloorina illite was pure and contained 9.2% Fe, 93% of which was Fe(III). Illite suspensions were buffered at pH 7 and were inoculated with CN32 cells with lactate as the electron donor. Select treatments included anthraquinone-2,6-disulfonate (AQDS) as an electron shuttle. Bioproduction of Fe(II) was determined by ferrozine analysis. The unreduced and bioreduced solids were characterized by Mössbauer spectroscopy, X-ray diffraction and transmission electron microscopy. The extent of Fe(III) reduction in the bulk Fithian illite was enhanced by the presence of AQDS (73%) with complete reduction of jarosite and goethite and partial reduction of illite. Mössbauer spectroscopy and chemical extraction determined that 21–25% of illite-associated Fe(III) was bioreduced. The extent of bioreduction was less in the absence of AQDS (63%) and only jarosite was completely reduced with partial reduction of goethite and illite. The XRD and TEM data revealed no significant illite dissolution or biogenic minerals, suggesting that illite was reduced in the solid state and biogenic Fe(II) from jarosite and goethite was either released to aqueous solution or adsorbed onto residual solid surfaces. In contrast, only 1% of the structural Fe(III) in Muloorina illite was bioreduced. The difference in the extent and rate of bioreduction between the two illites was probably due to the difference in layer charge and the total structural Fe content between the Fithian illite (0.56 per formula) and Muloorina illite (0.87). There may be other factors contributing to the observed differences, such as expandability, surface area and the arrangements of Fe in the octahedral sheets. The results of this study have important implications for predicting microbe-induced physical and chemical changes of clay minerals in soils and sediments.

Bentonite is to be used as a sealing material for long-term storage of radioactive waste. During permafrost periods the buffer may freeze, causing the following: montmorillonite dehydration, ice formation, and pressure build-up that may fracture the surrounding rock. No previous study has been done on freezing of bentonite in saline water. Using small and wide angle X-ray scattering, the present study aimed to increase understanding of the combined impact of salt and temperature on the hydration (swelling) of Wyoming montmorillonite. The basal spacing of the Na-montmorillonite was very dependent on the water content, while this was not the case for the Ca-montmorillonite (after reaching 19 Å). The basal spacing of the free-swelling Na-montmorillonite (34–280 Å) was estimated successfully using simple calculations. During freezing of Na-montmorillonite in NaCl solution, both ice and hydrohalite formed (at -50 and -100ºC). At starting concentrations ≥ 1.5 M the basal spacing was not affected by freezing. During freezing of Ca-montmorillonite in CaCl2 solution, ice formed; antarcticite formed only sporadically. The basal spacing of the Ca-montmorillonite at high NaCl concentrations (>1 M) was greater at -50 and -100ºC (18 Å) than at 20ºC (16 Å). The opposite was observed at low concentrations. This change was attributed to small amounts of salts introduced into the montmorillonite interlayer, hence changing the interlayer water properties. The montmorillonite hydration was also temperature dependent; decreasing temperature increased the hydration (as long as no ice was formed) and increasing the temperature decreased the hydration. This was attributed to the temperature impact on the entropy of the hydration reaction. This observation was also reproduced in an experiment up to 90ºC. A small amount of salt in the groundwater was noted to reduce significantly the potential problem of ice formation in bentonite sealings.

Infrared (Visible-Near Infrared-Shortwave Infrared (VNIR-SWIR)) spectroscopy is a cost-effective technique for mineral identification in the field. Modern hand-held spectrometers are equipped with on-board spectral libraries that enable rapid, qualitative analysis of most minerals and facilitate recognition of key alteration minerals for exploration. Spectral libraries can be general or customized for specific mineral deposit environments. To this end, careful collection of spectra in a controlled environment on pure specimens of key minerals was completed using the National Mineral Reference Collection (NMC) of the Geological Survey of Canada. The spectra collected from specimens in the ‘Kodama Clay Collection’ were processed using spectral plotting software and each new example was validated before being added to a group of spectra considered for incorporation into the on-board library of the handheld ASD-TerraSpec Halo near-infrared (NIR) mineral identification instrument. Spectra from an additional suite of mineral samples of the NMC containing REE, U, Th, and/or Nb are being prepared for a new, publicly available spectral library. These minerals commonly occur in carbonatite or alkali intrusive deposits, and as such will assist in the exploration for critical metals.

The swelling property of smectite is dominated by the hydration of exchangeable cations in the interlayer spacing (‘interlayer hydration’). By investigating systematically the swelling behavior of various exchangeable cations with different valences and ionic radii, the interlayer hydration of smectite was explored. The swelling behavior of Li+-, K+-, Rb+-, Cs+-, Mg2+-, Sr2+-, Ba2+-, and La3+- montmorillonites in undersaturated conditions was measured precisely over the range 50–150°C by in situ X-ray diffraction (XRD) analyses. The systematic swelling behavior of ten homocationic montmorillonites, the aforementioned eight homoionic montmorillonites, plus Na+ and Ca2+ from a previous study, and the cation hydration energies were analysed by studying the changes occurring in the basal spacing and the 001 peak width. With decreasing cation hydration energy, swelling curves (i.e. plots of basal spacing vs. relative humidity (RH)) change from continuous (Mg2+, La3+, and Ca2+) to stepwise (Sr2+, Li+, Ba2+, and Na+) to one-layer only (K+, Rb+, and Cs+). For the first two groups, the RH at the midpoint between the one- and two-layer hydration states increased as the cation hydration energy decreased. Under low RH, with increasing temperature, the basal spacings of Mg-, La-, Ca-, Sr-, Li-, and Ba-montmorillonites decreased continuously to the zero-layer hydration state, whereas Na-, K-, Rb-, and Cs-montmorillonites swelled from the zero-layer hydration state even at the lowest temperature (50°C). A decrease in the basal spacing at the same RH but at different temperatures suggests the existence of metastable states or that the layer-stacking structure changes with temperature. The systematics of the swelling behavior of various homocationic montmorillonites as functions of RH and temperature (<150°C) at 1 atmare reported here.

We report on how the effects of mechanical compaction and clay mineral diagenesis have affected the alignment of phyllosilicates in a suite of Miocene-Pliocene mudstones buried to sub-seabed depths of between 1.8 and 5.8 km in the deep-water Gulf of Mexico. Mechanical compaction has reduced the porosity of the samples to 15% at 5 km, with modal pore sizes between 10 and 20 nm. High-resolution X-ray texture goniometry data show that the intense mechanical compaction has not resulted in a strongly aligned phyllosilicate fabric. The muds were apparently deposited with a weak or isotropic phyllosilicate fabric which was not substantially realigned by mechanical compaction. Unusually, X-ray diffraction of <0.2 µm separates shows that: (1) there is no illitization trend between 90 and 120°C; and (2) discrete smectite persists to ∼120°C, coexisting with R1 I-S or R0 I-S with 30–40% expandable layers. Between 120 and 130°C, discrete smectite disappears and the expandability of I-S decreases to ∼25–30%. We propose a two-stage diagenetic process involving (1) the alteration of volcanic glass to smectite and (2) the illitization of smectite and I-S; the alteration of glass results in smectite without a preferred orientation and retards the illitization reaction. We suggest that the lack of a strongly aligned phyllosilicate fabric reflects the apparently limited extent of illitization, and thus recrystallization, to which these mudstones have been subjected.

A number of organobentonites were synthesized by exchanging the metal ions in bentonite with the cationic surfactant, cetyltrimethylammonium bromide. Samples of natural bentonite and organobentonites were analyzed for their organic carbon contents, examined by X-ray diffraction (XRD) for interlayer spacings, and viewed using a scanning electron microscope (SEM) for surface morphology. The sorption isotherm of benzene vapor from ambient air (relative humidity (RH) = 45 ± 5%) on natural bentonite was nonlinear; however, the isotherms of benzene from ambient air onto organobentonites were virtually linear over a large range of relative vapor concentrations. The sorption capacities of air-dried organobentonites were far greater than that of the natural bentonite. For air-dried organobentonites, the sorption coefficients correlated positively with the sample organic carbon contents and negatively with the sample BET-N2 surface areas. The heats of benzene vapor sorption onto air-dried organobentonites were less exothermic than the heat of benzene-vapor condensation. These findings suggest that benzene vapor sorption by air-dried organobentonites occurs essentially by vapor partition into the sample organic-matter fractions. This offers a potential application of organobentonites for the removal of organic vapors from flue gases and for assessing the efficiency of vapor removal.

Adsorption of uranyl (UO22+) ions to mineral surfaces is a potentially effective method for removing this hazardous metal from water, but other toxic trace metal ions (Xn+: Rb+, Sr2+, Cr3+, Mn2+, Ni2+, Zn2+, Cd2+) in uraniferous wastewaters compete with UO22+ for adsorption sites and thus may diminish the capacity of adsorbents to sequester UO22+. A better understanding of competitive adsorption among these metal ions and the development of better adsorbents are, therefore, of critical importance. The purpose of the present study was to synthesize and characterize magnetic adsorbents, consisting of MFe2O4 (M = Mn, Fe, Zn, Co, or Ni) nanoparticles synthesized on montmorillonite (Mnt) edge sites, and to investigate their use as adsorbents for UO22+, including competitive adsorption with trace metal ions. Selective adsorption was studied using Langmuir, Freundlich, and Dubinin-Radushkevich isotherms, and the results showed that Xn+ ions were adsorbed primarily on MFe2O4-montmorillonite surfaces, and the UO22+ ions were adsorbed on the interfaces between montmorillonite edge surfaces and MFe2O4 nanoparticles. Using the Freundlich model, the interface adsorption capacity of UO22+ reached 25.1 mg·g–1 in mixed solution. Further, the UO22+ and Cr3+ ions had a redox reaction on the interfaces with synergistic adsorption. Herein, the adsorption capacity of Cr3+ was 60.2 mg·g–1 using the Freundlich isotherm. The results demonstrated that the MFe2O4-montmorillonite with highly selective adsorption of UO22+ ions is applicable to UO22+ treatment in the presence of toxic trace metal ions.

Graphical abstract

In Iran, the writing of history has consistently been intertwined with political decisions, and official historiography written after the Islamic Revolution is no exception. The majority of books and articles on Pahlavi I have inherited this historiographic tradition, and are thus highly politicized, particularly around the topic of the role of the clergy during this era. Official narratives of this period are based on two representations: portraying intellectuals and Britain as the sole forces involved in bringing Reza Shah to power and consolidating his rule, while concealing the role of the clergy, or depicting this social group as the sole opposition to his government. This article aims to assess this binary narrative and answer the following question: What role did the clergy play in establishing and consolidating Reza Shah's reign? Research findings indicate that neither of these claims are accurate, as the clergy played a key role in the transfer of power from the Qajar to Pahlavi dynasties by supporting Reza Khan during his ministry, participating in the coup on February 22, 1921 (3 Esfand 1299), and supporting him in the Constituent Assembly. Further, the majority of clergy not only did not play the role of opposition, but indeed actively participated in the governmental institutions of the era. This research utilizes a historical-documentary approach to examine the subject.

Boron and lithium were analyzed in three nanometer-sized (<20, 20-50 and 50-100 nm) separates of two Santonian (85.8-83.5 Ma) bentonite samples collected closely in the Campos Basin along the southeastern Atlantic coast (Brazil). The B and Li data give various trends that suggest varied crystallization conditions for separates that consist of overwhelming smectite with less than 9% illitic layers. The δ11B of the few illitic tetrahedral sites from one of the samples remains quite constant, while its contents are strictly correlated with those of K, which suggests that illitization proceeded by interaction with pore fluids of the host sediments that supplied the K. In the second sample, the δ11B of the illite layers from the two coarser fractions is indicative of an early volcanic origin, while the smaller size fraction also interacted with sedimentary fluids. Favored by octahedral substitutions of the smectite layers, the δ7Li is more strictly regulated by a volcanic link. In turn, the information of the B and Li isotopic compositions and contents from studied mixed-layers suggests a various origin for the few illite layers of the smectite-rich I-S that contain more B than the smectite layers that host more Li. The difference appears to be sample-site and crystal-size dependent, fueled by pore fluids of the hosting turbidites.

The Brunauer-Emmett-Teller (BET) theory models the effective specific surface area and water content of solids as a function of the relative vapor pressure of water. A modified form of the BET equation has been used successfully to model water activity in concentrated electrolyte solutions as a function of electrolyte concentration. This modified form, referred to here as the Stokes-Robinson BET model, is based on the electrolyte molality rather than on the mass of solute sorbed. The present study evaluates the Stokes-Robinson form of the BET equation to model water-sorption data on two smectites with different layer charges. One smectite was saturated with Na+ and another with Na+, Ca2+, or Mg2+. These results are compared to the Stokes-Robinson BET results of aqueous electrolyte solutions. Given published data on cation exchange capacities and water-vapor sorption isotherms for various clays, the molality of the aqueous phase in contact with the clay surface is calculated and related to water activity. The Stokes-Robinson BET model was found to describe accurately the water activity as a function of cation molality below water activities of 0.5 for the smectites. Good relative agreement was obtained between the number of water binding sites predicted by the model and the experimental data reported in the literature for other smectites. Water molecules were found to have a significantly greater affinity for montmorillonite than electrolyte solutions with the same cation molality as the montmorillonite interlayer. This modified BET approach simplifies water-activity modeling in highly saline environments because the same equation can be used for both the liquid- and mineral-surface phases.

Accidents are a prevalent feature of working in the maritime industry. While studies have shown to what extent accidents and fatalities have occurred, the current research has generally been limited to commercial shipping. There is nearly no academic research focusing on the safety issues in the superyacht industry. This paper analyses the importance of promoting safety culture in the superyacht industry, the role of maritime legislation in maintaining safety and the role of Port State Control in ensuring all legislation is implemented. It aims to provide a critical examination of safety culture in the superyacht industry and evaluate the appropriateness for further measures to ensure safe working practices. It found out that while some superyachts do maintain an effective safety system, there remains almost 50% of the investigated fleet that do not promote the desired safety culture. It becomes evident that complacency and poor education contribute to the reduced and limited safety culture. The lack of education and awareness is demonstrated when the study shows individuals believing they maintain good safety practices but still admitting to taking various life-threatening risks.