Chloride Solution Research Articles

Ultrahigh tribocorrosion resistance of hydrogenated amorphous carbon coating via trace gradient W incorporation

In this work, we manipulated the trace gradient W incorporation combined with a increment top-layer thickness for the hydrogenated amorphous carbon (a-C:H) coating on thermally sprayed WC-based cermet. The tribocorrosion resistance of the modified a-C:H coating was investigated in terms of structural evolution during friction under 3.5wt.% NaCl solution. Regardless of introduction of gradient W doping, although the a-C:H coating maintained the sp2/sp3 atomic bond structure, the stress reduction and plasticity increase were obtained for coatings. Moreover, the stable open-circuit potential revealed that the tribocorrosion resistance of modified coating was significantly improved, as identified by the quite low wear rate and coefficient of friction at 1.46×10-8 mm3/N·m and COF of 0.067, respectively. Different with the traditional failure of worn-out and pitting corrosion of a-C:H coating in chloride solution, the designed robust interfaces and the functional top-layer enabled the coating to withstand longest sliding distance over 2100m at heavy contacting pressure of 1.67GPa. These observations offer the promising strategy to fabricate advanced carbon-based coatings with required extremely strong wear resistance and anticorrosion capability for mechanical components used in harsh marine environment.

Study on solubility and solvation thermodynamics for the advancement of biorelevant activities of l-isoleucine and l-serine in aqueous ammonium chloride solutions in the temperature range of 288.15–308.15 K

This study investigated the dissolution behavior of l-isoleucine and l-serine in an aqueous salt solution (ammonium chloride), examining how variations in temperature and electrolyte concentration affect their solubility. We conducted careful experiments and used mathematical calculations to explore interactions at a molecular level. We observed that the structure of these amino acids and salt concentration in the aqueous medium influence their interactions, which affects dissolution. In the presence of electrolytes, l-isoleucine demonstrated a salting-out effect whereas l-serine showed a salting-in effect. This work examines the solute–solvent interactions of these solutes in aqueous ammonium chloride solutions. l-isoleucine exhibits a nonspontaneous reaction with increasing salt concentrations whereas l-serine shows spontaneous behavior. Gibbs free energy analysis revealed greater stability of l-serine. The pH and conductance measurements showed how these factors influence solution properties. This insight helps us comprehend the nature and behavior of these molecules in different situations, which could be helpful in drug formulation or protein purification in the future.

Robust, transparent, self-healable, recyclable all-starch-based gel with thermoelectric capability for wearable sensor

Conventional all-starch-based (ASB) gels are weak and lack ductility. The preparation of a robust ASB gel with multi-functionalities e.g., self-healing, anti-freezing, conductivity, and so forth, is highly desirable but challenging. Herein, a new kind of ASB gel was prepared by gelatinizing starch in urea and choline chloride solution (UC) with the aid of water. Its tensile strength was up to 1.08 MPa with a tensile strain of 313 %, and this value hardly changed after 10 days ageing. A high healing efficiency of 98 % can be achieved after 1 h of healing at room temperature, and the healed tensile strength reaches up to ca. 1.06 MPa, which is almost the highest value for ASB gel. The resultant ASB gel can surfer from bending and twisting at −80 °C. Moreover, ASB gel also exhibits excellent biocompatibility and biodegradability. In addition, UC endowed the ASB gel with ion conductivity, allowing it to be used as a flexible strain sensor to monitor human movement. The ion-conductive ASB gel also exhibited thermoelectric ability with a Seebeck coefficient of 2.5 mV K−1, which can be further improved to 5 mV K−1 with a maximum output voltage of 252 mV by introducing a gradient of ionic concentration.

Initial stages of silver electrodeposition on a model Pt(111) single-crystal substrate from ethaline

Deep eutectic solvents (DES) are a new class of solvents with unique properties that are very promising media for the electroplating of metals and alloys. Knowledge about the regularities of metal electrodeposition is noticeably promoted by studies on model single crystal electrodes with a known well-ordered surface structure. In this work, we investigate the regularities of under- and overpotential deposition (upd and opd, respectively) of silver from a silver chloride solution in ethaline on a Pt(111) single crystal surface. For a better understanding of the occurring processes, we employ a complex approach involving electrochemical and in situ and ex situ microscopic techniques. We show that the process of gradual surface poisoning is observed on Pt(111) in the potential range in which no massive solvent degradation is yet observed. We also observe that the extent of this process largely depends on the employed potential of contact between the electrode and the solution and the studied potential range.The presence of Ag upd on Pt(111) in ethaline is demonstrated using voltammetric and in situ STM data. The available results and charge analysis are used to compare the Ag upd processes in ethaline and in aqueous solutions. We discuss the number of Ag adlayers on Pt(111), the effect of the potential of initial contact of the electrode with the solution and cycling history, and the possibility of anion upd and formation of coadsorbate between Ag adatoms and upd chloride anions (chlorine adatoms). We also demonstrate that upd Ag is not completely desorbed until high anodic potentials, where it seems to catalyze the solvent oxidation. Phase deposition of silver from ethaline on Pt(111) starts at almost zero overpotentials, which is probably related to the presence of the already deposited Ag adlayer. Even at very low overpotentials the deposit includes both large planar 2D crystallites and 3D crystallites formed on the surface defects and at the edges of the flat deposit islands. As the overpotential grows, the epitaxiality is gradually lost; the deposit becomes unshaped and the amount of 3D crystallites and their height increase

Effect of Chloride Solution on Liquid Limit, and Plasticity Index of Soil in Selected Sites in Erbil /North Iraq

This study is an attempt to investigate the effect of NaCl, CaCl2, KCl, and NH4Cl solutions with different concentrations (2.5%, 5%, 7.5%) on the liquid limit, plastic limit, and plasticity index of Sarbasty and Mamwastayan soil samples /Erbil Governorate. The soil samples' liquid and plastic limits were found by using the cone penetrometer method. The Results showed that the soil's liquid, plastic limits, and Plasticity index decreased with increasing salt solution concentration. Maximum reduction of liquid limit and plastic limit in Sarbasty was from 53.6 to 34.3 and in Mamwastayan from 35.9 to 27.2, both accomplished by adding a concentration of 7.5% of KCl and CaCl2 respectively. According to the Unified Soil Classification System, the Sarbasty soils were classified as high plasticity clay (CH), and Mamwastayan low plasticity clay (CL). After adding different concentrations of salt solution to the soil, the Sarbasty soil classification changed from CH to CL. Mineralogically these soils are composed of non-clay minerals of calcite and quartz and clay minerals consisting of Montmorillonite, Chlorite, swelling Chlorite, Kaolinite, Illite, Palygorskite, and Illite- Chlorite. Sarbasty soil was the most effective salt chloride solution than the Mamwastayan soil sample swelling.

Beach wrack as a potential microplastic hot spot in the South-Eastern Baltic Sea environment

Beach wrack is considered as a major source of nutrients to the sandy coast ecosystems in the South-East Baltic Sea, and it serves as the natural beach sediment storage and habitat formation material. However, it also could be a hot spot for microplastic and other types of marine litter accumulation. We carried out the recovery rate experiments to determine the most reliable method for a rapid and cost-effective application to extract microplastics from the beach wrack. The aeration of media in a saturated solution of sodium chloride revealed to be statistically significant and reliable, therefore was selected as a most suitable to extract the microplastics from the beach wrack. This study shows that the concentration of microplastics is significantly different between the four analyzed compartments in the coastal zone. The microplastic concentration in a beach wrack, with a mean value of 0.47 ± 0.17 items/cm3, contained 4.7 times more microplastics than observed in the surface sand samples. This study estimated that on average over 450 million microplastic items could be found during the castaway event in the South-East Baltic Sea coast.

Harnessing the potential of deep eutectic solvents in biocatalysis: design strategies using CO2 to formate reduction as a case study

IntroductionDeep eutectic solvents (DESs) have emerged as green solvents with versatile applications, demonstrating significant potential in biocatalysis. They often increase the solubility of poorly water-soluble substrates, serve as smart co-substrates, modulate enzyme stereoselectivity, and potentially improve enzyme activity and stability. Despite these advantages, screening for an optimal DES and determining the appropriate water content for a given biocatalytic reaction remains a complex and time-consuming process, posing a significant challenge.MethodsThis paper discusses the rational design of DES tailored to a given biocatalytic system through a combination of experimental screening and computational tools, guided by performance targets defined by solvent properties and process constraints. The efficacy of this approach is demonstrated by the reduction of CO2 to formate catalyzed by NADH-dependent formate dehydrogenase (FDH). By systematically analyzing FDH activity and stability, NADH stability (both long-term and short-term stability after solvent saturation with CO2), and CO2 solubility in initially selected glycerol-based DESs, we were able to skillfully guide the DES screening process.Results and discussionConsidering trade-offs between experimentally determined performance metrics of DESs, 20% solution of choline chloride:glycerol in phosphate buffer (ChCl:Gly80%B) was identified as the most promising solvent system for a given reaction. Using ChCl:Gly as a co-solvent resulted in an almost 15-fold increase in FDH half-life compared to the reference buffer and stabilized the coenzyme after the addition of CO2. Moreover, the 20% addition of ChCl:Gly to the buffer improved the volumetric productivity of FDH-catalyzed CO2 reduction in a batch system compared to the reference buffer. The exceptional stability of the enzyme in this co-solvent system shows great potential for application in continuous operation, which can significantly improve process productivity. Additionally, based on easily measurable physicochemical solvent properties and molecular descriptors derived from COSMO-RS, QSAR models were developed, which successfully predicted enzyme activity and stability, as well as coenzyme stability in selected solvent systems with DESs.

Paintable, Fast Gelation, Highly Adhesive Hydrogels for High-fidelity Electrophysiological Monitoring Wirelessly.

High-fidelity wireless electrophysiological monitoring is essential for ambulatory healthcare applications. Soft solid-like hydrogels have received significant attention as epidermal electrodes because of their tissue-like mechanical properties and high biocompatibility. However, it is challenging to develop a hydrogel electrode that provides robust contact and high adhesiveness with glabrous skin and hairy scalp for high-fidelity, continuous electrophysiological signal detection. Here, a paintable, fast gelation, highly adhesive, and conductive hydrogel is engineered for high-fidelity wireless electrophysiological monitoring. The hydrogel, consisting of gelatin, gallic acid, sodium citrate, lithium chloride, glycerol, and Tris-HCl buffer solution exhibits a reversible thermal phase transition capability, which endows it with the attributes of on-skin applicability and fast in situ gelation with 15 s, thereby addressing the aforementioned limitations. The introduction of gallic acid enhances the adhesive properties of the hydrogel, facilitating secure electrode attachment to the skin or hairy scalp. To accentuate the potential applications in at-home electrophysiological health monitoring, the hydrogel electrodes are demonstrated for high-fidelity electrocardiogram recording for one hour during various daily activities, as well as in simultaneous electroencephalogram and electrocardiogram recording during a 30 min nap.

Managing earliness and yield of cotton by modulating plant population, foliar boron feeding and mepiquat chloride application

ABSTRACT Early maturity and simultaneous increase in yield of cotton are pivotal for increasing the productivity of cropping systems involving cotton. Current two-year study was performed to simultaneously enhance the earliness and yield of cotton by modulating plant population (PP) (5.3 and 8.8 plants m−2), foliar boron (B) (0, 0.6 and 1.2 g/L B) and 0.07 g/L mepiquat chloride (MC) solution (at squaring and flowering stages) application. Internodes length was exalted at high PP (8.8 plants m-2) and B (1.2 g/L B), while declined by MC. Nevertheless, nodes above the white flower and cracked boll were decreased at high PP, and the application of B and MC indicated earlier cutout. Similarly, high PP, and application of 1.2 g/L B and MC at squaring reduced calendar and thermal time needed for flowering and boll opening. The boll maturation period was not affected by the application of B and MC but declined at high PP. Earliness index, production rate index (PRI) and seed cotton yield were increased at high PP, application of 1.2 g/L B and MC at squaring. In crux, increasing PP and B concentration, and MC application at squaring resulted in early maturity and enhanced seed cotton yield by modulating plant structure and time required for various phenophases.

Nanoflower-like NiCoFe layered hydroxide by in-situ electrochemical corrosion as highly efficient electrocatalyst for water oxidation

Layered double hydroxides have been widely applied for oxygen evolution reaction (OER) in the alkaline water electrolysis. However, the issues of poor connection between the catalyst and nickel foam and the specific mechanisms for active sites has not been fully documented. In this study, the in-situ nickel foam etching in a mixed solution of ferric chloride and cobalt nitrate at low temperatures was adopted for NiCoFe layered ternary hydroxides (NiCoFe LTHs) synthesis with a better tight integration. Physicochemical characterization indicated that the NiCoFe LTHs could grow directly through corroding nickel foam with a nano-flower-like morphology and structures. That is favorable for electron transfer from the catalytic layer to the conductive substrate. With the transition metal ions interaction and the tight integration construction, NiCo1Fe4-LTH-T60/NF presented an enhanced electrolysis performance with the overpotential of 234 mV (1.464 V vs. RHE) at current density of 100 mA cm−2 in 1 M KOH electrolyte. The Tafel slope for NiCo1Fe4-LTH-T60/NF electrode was 36.19 mV dec−1 for an enhanced OER kinetics. Besides, it demonstrated faster interfacial charge transfer process, better intrinsic electrochemical activity and stability in large current stability testing. It was revealed that the synergistic effect of the transition metal ions interaction enhancement and the mechanism of oxygen evolution elementary reaction for NiCo1Fe4-LTH-T60/NF during the water electrolysis by the electrochemical and theoretical calculation. This work provides theoretical basis and experimental support for the design and synthesis of future OER catalyst and substrate, which is significant for hydrogen and oxygen generation from water electrolysis.

Frequency–Time Domain Analysis Based on Electrochemical Noise of Dual-Phase (DP) and Ferrite–Bainite (FB) Steels in Chloride Solutions for Automotive Applications

The automotive industry uses high-strength (HS), low-alloy (HSLA) steels and advanced high-strength steels (AHSSs) to manufacture front and rear rails and safety posts, as well as the car body, suspension, and chassis components of cars. These steels can be exposed to corrosive environments, such as in countries where de-icing salts are used. This research aims to characterize the corrosion behavior of AHSSs based on electrochemical noise (EN) [dual-phase (DP) and ferrite–bainite (FB)]. At room temperature, the steels were immersed in NaCl, CaCl2, and MgCl2 solutions and were studied by frequency–time domain analysis using wavelet decomposition, Hilbert–Huang analysis, and recurrence plots (RPs) related to the corrosion process and noise impedance (Zn). Optical microscopy (OM) was used to observe the microstructure of the tested samples. The results generally indicated that the main corrosion process is related to uniform corrosion. The corrosion behavior of AHSSs exposed to a NaCl solution could be related to the morphology of the phase constituents that are exposed to solutions with chlorides. The Zn results showed that DP780 presented a higher corrosion resistance with 918 Ω·cm2; meanwhile, FB780 presented 409 Ω·cm2 when exposed to NaCl. Also, the corrosion mechanism of materials begins with a localized corrosion process spreading to all the surfaces, generating a uniform corrosion process after some exposition time.

Eliminating the «memory effect» during mass spectrometric determination of mercury

When estimating mercury content by inductively coupled plasma mass spectrometry (ICP-MS), this element adsorbs on the surface of the sample introduction system of the instrument, which creates problems in the determination of trace amounts of mercury. Various methods of cleaning the instrument have been proposed in the literature. Objective: to experimentally compare the effectiveness of trace mercury removal methods proposed in the literature for elemental analysis by ICP-MS and to select the optimal cleaning agent. Methods: Mercury content in solution was determined by the Agilent Technologies 7900 inductively coupled plasma mass spectrometer using 202Hg isotope. Diluted solutions of nitric and hydrochloric acids, solutions of gold chloride, potassium dichromate, thiourea, L-cysteine, potassium bromide, potassium bromate of different concentrations in water and 1% nitric and hydrochloric acids, aqueous solution of ammonium pyrrolidinedithiocarbomate were used as washing agents. Results: The background level of mercury content is achieved by using solutions of copper chloride (5%), thiourea (0.01, 0.1, and 0.5%), L-cysteine (2%), potassium bromide and bromate (0.0005 M) in 1.0% hydrochloric acid solution. The background is lowered by using 3 and 5% HCl, potassium dichromate (60 mg/liter), potassium bromide and bromate (0.01 and 0.05 M) solutions in 1% hydrochloric acid. Application of aqueous solution of ammonium pyrrolidinedithiocarbamate causes sharp degradation of plastic tubes of the sample introduction system. Conclusion: The efficiency of washing agents based on hydrochloric acid is higher than that based on nitric acid and water. The most promising washing agents are bromide-containing solutions and potassium bichromate solution in hydrochloric acid. The optimal way to clean the device is its washing with 0.5 mM potassium bromide solution in 1.0% hydrochloric acid. Its use allows to reduce the background content of mercury and does not complicate the analysis of the content of other elements.

Isothermal compressibility and water self-diffusion coefficient in supercooled salt aqueous solutions using the Madrid-2019 model

The isothermal compressibility and self-diffusion coefficient of water in Li + , Na + , K + , Mg 2 + and Ca 2 + chloride and sulfate salts aqueous solutions is calculated by means of molecular simulations using the Madrid-2019 force-field, that uses TIP4P/2005 model for water and assigns scaled charges for ions. Our simulations predict that the isothermal compressibilities of these salts retain the anomalous behaviour of water, i.e. compressibility increases as temperature decreases, contrary to the behaviour of normal liquids. A maximum in the isothermal compressibility, analogous to that of pure water, is observed for some of the salt solutions. For the 1 m NaCl solution, simulations are performed at several pressures up to 1000 bar to estimate the location of the second critical point. We estimate that the liquid-liquid critical point is located at 190 K and 1000 bar, i.e. it is shifted to slightly higher temperatures and lower pressures with respect to the most accurate estimation of its location in pure TIP4P/2005 water (172 K and 1861 bar). Regarding the self-diffusion of water, all salts increase water mobility in the very supercooled regime (at temperatures within 200–230 K), with K 2 SO 4 producing the largest increase in water mobility, while MgCl 2 and MgSO 4 are the least effective in enhancing the self-diffusion coefficient of water.

Effect of Anions on Deformation of Gallium-Based Liquid Metal in Solution.

In this study, deformation behaviors of gallium-based liquid metals in acidified cupric sulfate or cupric chloride solutions with varying concentrations of chloride anion or sulfate anion were investigated to explore their potential applications in soft machines and electronics. Gallium-based liquid metals are known for their unique deformability, making them promising materials for various fields. Previous research has shown that deformation of the liquid metal can be achieved in the presence of acidified cupric or ferric salts. However, the specific influence of different anions on the deformation process remains unclear. Our findings indicate that the deformation rate of the liquid metal increases with higher concentrations of chloride ions and decreases with higher concentrations of sulfate ions in the solution. UV-vis absorbance spectra of the solutions were analyzed to identify the formation of hydrated cupric cations. It was observed that increasing the concentration of Cl- ions promotes the formation of cupric-chloro complexes, thereby reducing the concentration of hydrated cupric ions in the solution. Furthermore, the addition of sulfate ions to the solution enhances the ionic strength of the medium, leading to the dissociation of cupric-chloro complexes. Additionally, sulfate ions can form insoluble layers with gallium ions, which impede the deformation of the liquid metal. The deformation rate of the liquid metal was found to be inversely correlated with the concentration of cupric ions in the solution. These results provide valuable insights into the deformable behavior of gallium-based liquid metals and their potential applications in liquid metal-based soft robots. This study highlights the importance of understanding the role of different anions in the deformation process of liquid metals, shedding light on the design and optimization of soft machines and electronics utilizing these materials.

Fracture toughness of alkali-activated concrete subjected to aggressive environment

This study investigates the fracture toughness of alkali-activated granulated blast-furnace slag (GBFS)-based geopolymer concrete (GPC), non-activated slag cement concrete, and ordinary Portland cement (OPC) concrete in acidic, alkaline, and chloride solutions over six months. A total of 580 centrally straight-notched Brazilian disc (CSNBD) specimens were cast to assess pure mode-I (0°), pure mode-II (28.7°), and mixed-mode (15° and 45°) fractures under these conditions. Microstructural analyses (SEM) were performed to evaluate microstructural changes after six months of exposure. Results showed that GPC exhibited the lowest initial fracture toughness but the smallest reduction (7 %-11 % depending on the mode) across all environments, with slag cement concrete and OPC experiencing reductions of 11 %-14 % and 14 %-21 %, respectively, in acidic conditions. In alkaline environments, GPC showed a 3 %-6 % decrease in fracture toughness, while OPC and slag cement concrete showed reductions of 6 %-13 %. The gradient boosting regressor accurately predicted the failure load of CSNBD specimens, achieving an R² score of 0.948. Finally, SHAP sensitivity analysis identified concrete type, exposure time, and environment as critical input features, consistent with experimental results.

2M NaCl by XPS using monochromatic Al K α x rays

Cryo-XPS enables the study of many substances that are unsuitable for standard XPS analysis, such as moderately volatile liquids, biological samples, porous materials, and polymeric materials that may outgas significantly under ultrahigh vacuum conditions. In this article, XPS spectra of a 50 μl frozen droplet of 2M sodium chloride solution (NaCl) in Millipore water purified to 18.2 MΩ cm at 25 °C were obtained using an Al Kα (1486.6 eV) source with a quartz (1010) crystal monochromator through first order diffraction and irradiating the sample at 54.7° to the surface normal. The sample was sputter cleaned using a Gas Cluster Ion Source pre-acquisition to remove the minor layer of adventitious carbon contamination on the surface. Spectra of the principal lines include Na 1s, O 1s, and Cl 2p. Spectra of O KLL, Na KLL, Cl 2s, Na 2s, Na 2p, O 2s, and valence band were also acquired.

Boosting Erosion‐Corrosion Resistance: Collaborative Ni–P Electroless Deposition on Poly‐Amino‐Alcohol@Functionalized GO Matrices

AbstractIn recent years, protective coatings have become crucial in graphene‐based chemical studies. This research investigates the anticorrosive properties of coatings created by co‐depositing carbon compounds. Electroless Ni−P‐PAA@F‐GO coatings were applied to stainless steel by adding various amounts of PAA@F‐GO particles to the Ni−P bath. The coated samples were analyzed using X‐ray diffraction and micro‐hardness tests, revealing a peak hardness of 764 HV at 30 mg/L PAA@F‐GO, compared to 521 HV for standard Ni−P coatings. Corrosion performance was evaluated in a 3 % sodium chloride solution, showing that despite a higher corrosion‐erosion rate. Although the coated samples exhibited a corrosion‐erosion rate 4.7 times higher than untreated samples, the mass loss was notably more pronounced in the untreated samples. The study found that adding PAA@F‐GO particles improved corrosion resistance and durability, with optimal results at a specific particle concentration. The enhanced performance is attributed to the increased roughness, impermeability, and hydrophobicity of the functionalized graphene oxide.

Thermodynamically Traceable Calorimetric Results for Aqueous Sodium Chloride Solutions from T = (273.15 to 373.15) K up to the Saturated Solutions: Part 2 —The Quantities Associated with the Partial Molar Heat Capacity

AbstractIn previous articles (Partanen and Partanen in J. Chem. Eng. Data 65: 5226 − 5239 (2020), J. Solution Chem. 52: 1352 − 1385 (2023)), we presented a traceable and transparent three-parameter model for thermodynamic activity and enthalpy quantities in aqueous NaCl solutions. The model is based on extended Hückel equations with parameters B, b1, and b2 and it applies from T = 273.15 to 373.15 K up to the saturated solutions. These studies demonstrate that the model explains the literature data of almost all thermodynamic quantities including apparent and partial molar enthalpies within experimental error. In the model, the ion-size parameter in the Debye–Hückel equation, B, is regarded as a constant while the parameters of the coefficients of the linear and quadratic molality terms, b1 and b2, respectively, possess quadratic temperature dependences. In this study, the results obtained for the heat capacity quantities of NaCl(aq) are considered. We show that the available heat capacity literature for these solutions can be predicted at least satisfactorily up to the saturated solutions with our new model. Following this success, we supplement the existing thermodynamic tables with the new values for the relative apparent and partial molar heat capacities for NaCl solutions. It is likely that the new tables contain the most reliable values determined so far even though no calorimetric data were used in the parameter estimation of our model. Graphical Abstract

Inhibition sensitivity of invitro firefly bioluminescence quantum yields to Zn2+ and Cd2+ concentrations in aqueous solutions.

To elucidate the inhibition effects of Zn2+ and Cd2+ on the luciferin-luciferase reaction, we performed quantitative measurements of quantum yields and spectral shapes for invitro firefly bioluminescence in aqueous solutions containing ZnSO4, ZnCl2, CdSO4, and CdCl2 at different concentrations. Particular care was taken toward the equilibrium between metal ions and enzyme proteins, anion difference, solubility, and uncertainty evaluation. The bioluminescence quantum yields decreased almost linearly to the concentration of Zn2+ and Cd2+ below 0.25 mM. No obvious difference was found between the chloride and sulfate anion solutions. We defined inhibition sensitivity as the decrease in relative quantum yield versus the concentration of metal ions, and they were determined to be 1.48 ± 0.13 and 1.13 ± 0.16/mM for Zn2+ and Cd2+, respectively. We estimated the detection limit of inhibition effects as the concentration of metal ions that decrease relative quantum yields by 10%, which were 0.07 mM (4 ppm) and 0.09 mM (10 ppm) for Zn2+ and Cd2+, respectively. The shape of the bioluminescence spectra changed sensitively with the increase in Zn2+ concentrations. The bioluminescence peak energy for 0.10-mM Zn2+ was ~2.2 eV, while that for 0.25-mM Zn2+ was ~2.0 eV. The shape of the spectra changed less sensitively with the increase in Cd2+concentrations, and the peak energy was at ~2.2 eV for Cd2+ concentrations of 0.10 and 0.25 mM.

The collection and application of autologous amniotic fluid to cesarean delivery closure – a feasibility study

Amniotic fluid and amnion membranes have been used in surgery specialties to improve wound healing. The objective was to determine if amniotic fluid could be collected at cesarean delivery and then reapplied to the layers of the closure using the CeaLogic Specimen Collection and Ratio Applicator Kit. Autologous amniotic fluid from 20 subjects was collected at cesarean delivery using the collection kit, and then transferred to the applicator kit, mixed with calcium chloride solution, and applied directly to each of the surgical repair layers during closure. The Modified Hollander Cosmesis Score was used to assess wound appearance from photographs of the incision taken in the postpartum setting. The median (IQR) Modified Hollander Cosmesis Score (range 0-best, to 6-worst) at the one week and four-week postpartum visits was 0 (0,1) and 0 (0,2), respectively. There were no wound complications nor surgical site infections. The CeaLogic Specimen Collection and Ratio Applicator Kits can be used to collect and reapply autologous amniotic fluid at cesarean delivery. Future studies can determine if the application of autologous amniotic fluid to cesarean delivery closure can improve cosmesis and wound healing, as well as decrease the risk for the development of intraabdominal adhesions.