CO2 Elimination Research Articles

Engineering of oxygen vacancy and bismuth cluster assisted ultrathin Bi12O17Cl2 nanosheets with efficient and selective photoreduction of CO2 to CO

AbstractThe photocatalytic conversion of CO2 into solar‐powered fuels is viewed as a forward‐looking strategy to address energy scarcity and global warming. This work demonstrated the selective photoreduction of CO2 to CO using ultrathin Bi12O17Cl2 nanosheets decorated with hydrothermally synthesized bismuth clusters and oxygen vacancies (OVs). The characterizations revealed that the coexistences of OVs and Bi clusters generated in situ contributed to the high efficiency of CO2–CO conversion (64.3 μmol g−1 h−1) and perfect selectivity. The OVs on the facet (001) of the ultrathin Bi12O17Cl2 nanosheets serve as sites for CO2 adsorption and activation sites, capturing photoexcited electrons and prolonging light absorption due to defect states. In addition, the Bi‐cluster generated in situ offers the ability to trap holes and the surface plasmonic resonance effect. This study offers great potential for the construction of semiconductor hybrids as multiphotocatalysts, capable of being used for the elimination and conversion of CO2 in terms of energy and environment.

A quasi-experimental study of fresh oxygen flow on patients' oxygen reserve during mask-assisted ventilation under general anesthesia induction.

To compare the effect of different amounts of fresh oxygen flow on oxygen reserve in patients undergoing general anesthesia. Seventy-two patients were enrolled in this quasi-experimental study. Patients were randomly divided into experimental groups with a fresh oxygen flow of 1 L/min, 2 L/min, 4 L/min, and 8 L/min (denoted as G1, G2, G3, and G4, respectively) for 2 min of mask-assisted ventilation. Safe apnea time (SAT) was the primary endpoint; SAT was defined as the time from the cessation of ventilation to the time the patient's pulse oxygen saturation (SpO2) decreased to 90%. Ventilation indicators such as end-tidal oxygen concentration (EtO2), end-tidal carbon dioxide partial pressure (EtCO2), SpO2, and carbon dioxide (CO2) elimination amount, during mask-assisted ventilation, were the secondary endpoints. The SAT of G1, G2, G3, and G4 were 305.1 ± 97.0 s, 315 ± 112.5 s, 381.3 ± 118.6 s, and 359 ± 104.4 s, respectively (p > 0.05). The EtO2 after 2 min of mask-assisted ventilation in groups G1, G2, G3, and G4 were 69.7 ± 8.8%, 75.2 ± 5.0%, 82.5 ± 3.3%, and 86.8 ± 1.5%, respectively (p < 0.05). Also, there was a moderate positive correlation between the fresh oxygen flow and EtO2 (correlation coefficient r = 0.52, 95% CI 0.31-0.67, p < 0.0001). The CO2 elimination in the G1 and G2 groups was greater than that in the G4 group (p < 0.05). There was no significant difference in other indicators among the groups (all p > 0.05). The amount of fresh oxygen flow during mask-assisted ventilation was positively correlated with EtO2. Also, even though there was no significant difference, the patients' oxygen reserves increased with the increase in fresh oxygen flow.

Synergy of Epitaxial Layer and Bulk Doping Enables Structural Rigidity of Cobalt‐Free Ultrahigh‐Nickel Oxide Cathode for Lithium‐Ion Batteries

AbstractCobalt‐free ultrahigh‐nickel layered oxide cathodes hold great promise for reducing the cost and enhancing the energy density of Li‐ion batteries. However, the increasing Ni content and the elimination of Co could cause severe interfacial and structural degradation, leading to poor electrochemical performance of ultrahigh‐nickel layered oxide cathodes. Here, a Co‐free oxide, LiNi0.96Al0.03Ca0.01O2 (NAC), where Ca acts as pillar ions at the surface and Al works as an oxygen stabilizer across the bulk, is presented. An epitaxial layer rich in segregated Ca can effectively inhibit adverse surface reconstruction at high states of charge, together with the oxygen stabilization of bulk phase by doping Al, significantly reinforcing the structural rigidity of the layered oxide during cycling. The fabricated NAC cathode material exhibits exceptional electrochemical performance in terms of high cycling stability with 93% capacity retention over 500 cycles and a material‐level energy density of ~800 Wh kg−1. This study provides an efficient and feasible strategy to design and stabilize ultrahigh‐nickel oxides for lithium‐ion batteries.

Insights into the underpinning effect of graphene in Cu1Mn10 on enhancing the low-temperature catalytic activity for CO oxidation

CO emission is a critical issue of industrial processes such as steel-smelting, cement manufacturing, and waste incineration. Catalytic oxidation based on Cu–Mn binary catalysts shows great potential for efficient removal of CO, whereas their practical applicability is limited by the inferior low-temperature catalytic activity and the high catalyst cost owing to a substantial quantity of Cu. In this study, doping graphene is designed to adjust the electron transfer capability to improve the low-temperature catalytic activity as well as reduce the amount of Cu, and thereby Cu1Mn10 catalysts doped with slight amounts of graphene (x%G-Cu1Mn10, x is 1∼5) were fabricated. It was found that the introduction of graphene could form effective electron transport channels to enhance the intermetallic interaction and oxygen vacancy generation, thus improving the low-temperature catalytic performance of the Cu1Mn10 catalyst. Among all the catalysts, 4%G-Cu1Mn10 exhibited the highest activity, achieving CO conversion of 92% at 110 °C at a weight hourly space velocity of 120,000 mL/(g∙h). The introduction of graphene also enabled the catalyst with excellent catalytic activity and stability at a relative humidity of 70%. Attractively, 4%G-Cu1Mn10 can be further loaded into the polyester fabric, presenting great application potentials in the effective elimination of CO during the dust removal process since the flue gas temperature in the dust collector is just around the T90% and the catalyst that is inside of fabric fiber rather than on the fabric surface can be rarely influenced by the dust. In general, doping graphene provides a facile method to enhance the low-temperature activities of the Cu–Mn binary catalysts and cut down the use of valuable Cu, showing great application potential.

Whole lung lavage decreases physiological dead space in patients with pulmonary alveolar proteinosis: two case reports

BackgroundPulmonary alveolar proteinosis (PAP) is a rare disease characterized by progressive accumulation of the alveolar surfactant. Whole lung lavage (WLL) using a high volume of warmed saline remains the standard therapy. However, no established bedside monitoring tool can evaluate the physiological effect of WLL in the perioperative period. Indirect calorimetry, which is generally used to measure resting energy expenditure, can detect carbon dioxide (CO2) production and mixed-expired partial pressure of CO2 breath by breath. In this physiological study, we calculated CO2 elimination per breath (VTCO2,br) and Enghoff’s dead space using indirect calorimetry and measured the extravascular lung water index to reveal the effect of WLL.Case presentationWe measured VTCO2,br, Enghoff’s dead space, and the extravascular lung water and cardiac indices before and after WLL to assess the reduction in shunt by washing out the surfactant. A total of four WLLs were performed in two PAP patients. The first case involved an Asian 62-year-old man who presented with a 3-month history of dyspnea on exertion. The second case involved an Asian 48-year-old woman with no symptoms. VTCO2,br increased, and the Enghoff’s dead space decreased at 12 h following WLL. An increase in the extravascular lung water was detected immediately following WLL, leading to a transient increase in Enghoff’s dead space.ConclusionWLL can increase efficient alveolar ventilation by washing out the accumulated surfactant. However, the lavage fluid may be absorbed into the lung tissues immediately after WLL and result in an increase in the extravascular lung water.

A modal definition of ideal alveolar oxygen.

In the three-compartment model of lung ventilation-perfusion heterogeneity (VA/Q scatter), both Bohr dead space and shunt equations require values for central "ideal" compartment O2 and CO2 partial pressures. However, the ideal alveolar gas equation most accurately calculates mixed (ideal and alveolar dead space) PAO2 . A novel "modal" definition has been validated for ideal alveolar CO2 partial pressure, at the VA/Q ratio in a lung distribution where CO2 elimination is maximal. A multicompartment computer model of physiological, lognormal distributions of VA and Q was used to identify modal "ideal" PAO2 , and find a modification of the alveolar gas equation to estimate it across a wide range of severity of VA/Q heterogeneity and FIO2 . This was then validated in vivo using data from a study of 36 anesthetized, ventilated patients with FIO2 0.35-80. Substitution in the alveolar gas equation of respiratory exchange ratio R with achieved excellent agreement (r2 = 0.999) between the calculated ideal PAO2 and the alveolar-capillary Pc'O2 at the modal VO2 point ("modal" Pc'O2 ), across a range of log standard deviation of VA 0.25-1.75, true shunt 0%-20%, overall VA/Q 0.4-1.6, and FIO2 0.18-1.0, where the modeled PaO2 was over 50 mm Hg. Modal ideal PAO2 can be reliably estimated using routine blood gas measurements.

CO2-Derived Nanocarbons with Controlled Morphology and High Specific Capacitance.

The conversion of CO2 to nanocarbons addresses a dual goal of harmful CO2 elimination from the atmosphere along with the production of valuable nanocarbon materials. In the present study, a simple one-step metallothermic CO2 reduction to nanocarbons was performed at 675 °C with the usage of a Mg reductant. The latter was employed alone and in its mixture with ferrocene, which was found to control the morphology of the produced nanocarbons. Scanning electron microscopy (SEM) analysis reveals a gradual increase in the amount of nanoparticles with different shapes and a decrease in tubular nanostructures with the increase of ferrocene content in the mixture. A possible mechanism for such morphological alterations is discussed. Transmission electron microscopy (TEM) analysis elucidates that the nanotubes and nanoparticles gain mainly amorphous structures, while sheet- and cloud-like morphologies also present in the materials possess significantly improved crystallinity. As a result, the overall crystallinity was preserved constant for all of the samples, which was confirmed by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) techniques. Finally, electrochemical tests demonstrated that the prepared nanocarbons retained high specific capacitance values in the range of 200-310 F/g (at 0.1 V/s), which can be explained by the measured high specific surface area (650-810 m2/g), total pore volume (1.20-1.55 cm3/g), and the degree of crystallinity. The obtained results demonstrate the suitability of ferrocene for managing the nanocarbons' morphology and open perspectives for the preparation of efficient "green" nanocarbon materials for energy storage applications and beyond.

Effect of external dead space removal on CO2 homeostasis in mechanically ventilated adult Covid-19 patients.

Patients with Covid-19 respiratory failure present with hypoxemia, often in combination with hypercapnia. In this prospective, observational study we examined the effect of removing external dead space (DS) on CO2 -homeostasis in mechanically ventilated Covid-19 patients. In addition, volumetric capnography was validated for its ability to estimate external DS volume using in vitro measured DS volumes as reference. In total, 10 patients with acute respiratory distress syndrome from Covid-19 were included. Volumetric capnography, mechanical ventilation, and arterial blood gas data were analyzed before and after removal of external DS and analyzed for potentially significant changes in response to DS removal. Measurements of external DS were obtained in circuit using volumetric capnography and compared to actual measured DS volumes off the circuit. After the removal of external DS, the alveolar minute ventilation and CO2 elimination improved, notwithstanding unchanged respiratory rate and tidal volumes. The increase in CO2 elimination was associated with a decrease in arterial CO2 partial pressure (PaCO2 ). The volumetric capnography method for assessment of external DS showed a low bias of -9 mL (lower limit of agreement -40, 95% CI -60 to -20 mL, upper limit of agreement 21 mL, 95% CI: 1-40 mL) and a percentage error of 48% compared to absolute values measured in vitro. Removal of external DS increased alveolar minute ventilation and CO2 elimination in Covid-19 patients with respiratory failure in the current study. This was associated with a decrease in PaCO2 . This may indicate a decreased CO2 production due to decreased work of breathing and more effective gas-exchange in response to DS removal. In addition, volumetric capnography appears to be a clinically feasible method for continuous measurement of external DS in the current study and may be of value in optimizing ventilator treatment.

PULM5: Hyperbaric Blood Oxygenation – Basic Considerations and First Results

Hyperbaric oxygen therapy is beneficial in several applications, but hyperbaric chambers are scarce. We are developing a novel technology for extracorporeal hyperbaric blood oxygenation (HBOX). This extracorporeal procedure uses pressure to increase the oxygen (O2) concentration in blood. The technology can provide support when large amounts of oxygen are needed: In the treatment of CO poisoning the dissolved oxygen displaces the CO from the blood, removing it from the organism. This way, the oxygen deficiency can be ended rapidly, reducing or preventing secondary damage that frequently occurs. In acute respiratory failure (ARF) the HBOX technology can support lung function, by significantly increasing oxygen transport across a specific membrane area, while maintaining adequate CO2-removal. The prototype of the HBOX consists of 2 roller pumps with a hollow-fiber membrane oxygenator (HFMO) placed in between, a control unit for gas and blood flow and a double lumen catheter. By varying the flow rates of the roller pumps, excess pressure is generated in the HFMO without causing significant blood damage. Simultaneously, the oxygen pressure in the HFMO is increased, allowing for hyperbaric oxygenation. To avoid bubble formation, either O2 increase is limited, or excess O2 is removed in second HFMO before reinfusion. The prototype was tested in-vitro using porcine blood that was either CO poisoned or conditioned to mimic ARF. In acute in-vivo experiments for CO poisoning, we used CO-poisoned pigs (ca. 75 kg, COHb = 43 %, n = 3). For in-vivo experiments for ARF, 70 kg sheep were used with ventilator settings simulating respiratory failure, resulting in SaO2 = 69 %, paCO2 = 72 mmHg (n = 2). In-vitro test results show that the HBOX can fully oxygenate hypoxic blood (sO2 ca. 40 %) with a hilite 800 LT at a flow rate of 2 L/min, which is twice the amount of oxygen transferred, compared to conventional mode, Fig. 1. In in-vivo trials, the CO elimination rate from the animals’ blood doubled when using HBOX + oxygen mask compared to oxygen mask alone, see Fig. 2. In the ARF trials, the HBOX approach resulted in SaO2 of 89, 95, and 99 % and paCO2 was 49, 46, and 39 mmHg at blood flows of 0.5, 1.0, and 1.5 L/min, respectively, see Fig. 3. The HBOX is a promising approach to increase oxygen transport across a specific membrane area. The increased oxygen levels can be used for efficient extracorporeal CO removal. For respiratory support, the hyperbaric technology adds a new dimension to ECMO treatment, allowing the use of smaller oxygenators, potentially reducing the need for anticoagulation, as well as inflammatory responses and thus invasiveness. The hyperbaric technology can be used gradually, so that the membrane efficiency can be increased during intervention. This allows us to build an oxygenator with an ideal flow distribution over a wide range of blood flows, which avoids thrombus formation in the device at lower blood flows.Figure 1. Laboratory results oxygenation performanceFigure 2. Elimination rate COHb in in-vivo trialsFigure 3. Arterial blood gases during in-vivo trial for ARF

Unsupervised classification of plethysmography signals with advanced visual representations.

Ventilation is a simple physiological function that ensures the vital supply of oxygen and the elimination of CO2. The recording of the airflow through the nostrils of a mouse over time makes it possible to calculate the position of critical points, based on the shape of the signals, to compute the respiratory frequency and the volume of air exchanged. These descriptors only account for a part of the dynamics of respiratory exchanges. In this work we present a new algorithm that directly compares the shapes of signals and considers meaningful information about the breathing dynamics omitted by the previous descriptors. The algorithm leads to a new classification of inspiration and expiration, which reveals that mice respond and adapt differently to inhibition of cholinesterases, enzymes targeted by nerve gas, pesticide, or drug intoxication.

Li2ZrO3 modified with molten salts as potential materials for CO elimination: Effect of carbonate type and oxygen addition

It has been evaluated the effect of different types of carbonates on the catalytic activity of Li2ZrO3 during CO oxidation. Pure Li2ZrO3 was synthesized and mechanically modified with alkaline or metallic carbonates. Pure Li2ZrO3 and sodium-containing materials showed similar catalytic activity between 490 and 530 °C but not better than the pristine sample. Catalytic results under different O2/CO ratios showed that CO oxidation was not favored without O2, regardless of the catalyst used. A gas stream with excess O2 increments the catalytic performance, allowing to reach CO2 formations between 80 and 99% with pure and Li2ZrO3-NiCO3 samples, respectively. The most favorable effect due to NiCO3 addition was the reduction in the temperature for CO oxidation. Thus, the catalytic performance of the Ni-modified ceramic was the best, reaching conversions of 63 and 75% in low- and moderate-temperature ranges. None of these carbonate-modified materials captured the formed CO2.

Atmospheric chemistry of 2-nitrobenzaldehyde: Initiated by photo-excitation, OH-oxidation, and small TiO2 clusters adsorption catalysis

The fate of 2-nitrobenzaldehyde (2-NBA) is of interest in atmospheric chemistry as it is a semi-volatile organic compound with high photosensitivity. This study presents a quantum chemical study of the gas-phase reactions of 2-NBA photo-excitation and OH-oxidation in the absence and presence of small TiO2 clusters. To further understand the unknown photolysis mechanism, the photo-reaction pathways of ground singlet state and the lying excited triplet state of 2-NBA were investigated including the initial and subsequent reactions of proton transfer, direct CO, NO2, and HCO elimination routes in the presence of O2 and NO. Meanwhile, the OH-mediated degradation of 2-NBA proceeded via five H-extraction and six OH-addition channels by indirect mechanism, which follows a succession of reaction steps initiated by the formation of weakly stable intermediate complexes. The H-extraction from the –CHO group was the dominant pathway with a negative activation energy of -1.22 kcal/mol. The calculated rate coefficients at 200–600 K were close to the experimental data in literature within 308–352 K, and the kinetic negative temperature independence was found in both experimental literature and computational results. Interestingly, 2-NBA was favored to be captured onto small TiO2 clusters via six adsorption configurations formed via various combination of three types of bonds of Ti···O, Ti···C, and O···H between the molecularly adsorbed 2-NBA and TiO2 clusters. Comparison indicted that the chemisorptions of aldehyde oxygen have largest energies. The results suggested adsorption conformations have a respectable impact on the catalysis barrier. This study is significant for understanding the atmospheric chemistry of 2-nitrobenzaldehyde.

Haemolymph pH of two important mollusc species is susceptible to seawater buffering capacity instead of pH or pCO2

The acid-base status and balance of molluscs are considered to be susceptible to environmental changes, especially in the context of ocean acidification (OA). Here, we studied the effects of manipulated seawater carbonate chemistry on the acid-base status of scallop Chlamys farreri and abalone Haliotis discus hannai. The haemolymph pH of the tested individuals showed a fast response to acidified seawater incubation, and the pH level was restored to a normal value within 1 h of recovery in control seawater. However, no significant correlation (P > 0.05) was found between haemolymph pH and seawater pCO2 or pH, while the squared Pearson correlation coefficient (R2) ranged from close to zero to 0.41. In addition, although the pCO2 level of total alkalinity (TA)-lowered seawater was lower than half of that in the control, molluscs eliminated less CO2 (less than 80%) to TA lowered waters than to the control waters. These findings seem to disagree with the crucial role of seawater pCO2 in influencing the acid-base balance of molluscs. CO2 elimination occurs in the microenvironment, and CO2 first diffuses to limited amounts of seawater that tightly surround the gills, causing dissolved inorganic carbon (DIC) accumulation in the ventilation sites, which leads to a sharp increase in the pCO2 of the surrounding seawater. Moreover, in this microenvironment, the pCO2 level increases much faster and more greatly if the environmental seawater is acidified or contains a lower level of TA. Therefore, mollusc acid-base status is influenced by rapidly varying pCO2 levels at the ventilation site, which is largely independent of that of the rest of the incubating seawater. In summary, CO2 elimination by molluscs relies heavily on the carbonate chemistry of environmental seawater, and seawater buffering capacity should be taken into consideration instead of considering only pCO2 or pH in studying the acid-base balance of marine molluscs.

Reducing Pulmonary Capillary Wedge Pressure During Exercise Exacerbates Exertional Dyspnea in Patients With Heart Failure With Preserved Ejection Fraction: Implications for [formula omitted] Mismatch

The primary cause of dyspnea on exertion in heart failure with preserved ejection fraction (HFpEF) is presumed to be the marked rise in pulmonary capillary wedge pressure during exercise; however, this hypothesis has never been tested directly. Therefore, we evaluated invasive exercise hemodynamics and dyspnea on exertion in patients with HFpEF before and after acute nitroglycerin (NTG) treatment to lower pulmonary capillary wedge pressure. Does reducing pulmonary capillary wedge pressure during exercise with NTG improve dyspnea on exertion in HFpEF? Thirty patients with HFpEF performed two invasive 6-min constant-load cycling tests (20 W): one with placebo (PLC) and one with NTG. Ratings of perceived breathlessness (0-10 scale), pulmonary capillary wedge pressure (right side of heart catheter), and arterial blood gases (radial artery catheter) were measured. Measurements of V˙/Q˙ matching, including alveolar dead space (Vdalv; Enghoff modification of the Bohr equation) and the alveolar-arterial Po2 difference (A-aDO2; alveolar gas equation), were also derived. The ventilation (V˙e)/CO2 elimination (V˙co2) slope was also calculated as the slope of the V˙e and V˙co2 relationship, which reflects ventilatory efficiency. Ratings of perceived breathlessness increased (PLC: 3.43 ± 1.94 vsNTG: 4.03 ± 2.18; P= .009) despite a clear decrease in pulmonary capillary wedge pressure at 20W (PLC: 19.7 ± 8.2 vsNTG: 15.9 ± 7.4mmHg; P< .001). Moreover, Vdalv (PLC: 0.28 ± 0.07 vsNTG: 0.31 ± 0.08 L/breath; P= .01), A-aDO2 (PLC: 19.6 ± 6.7 vsNTG: 21.1 ± 6.7; P= .04), and V˙e/V˙co2 slope (PLC: 37.6 ± 5.7 vsNTG: 40.2 ± 6.5; P< .001) all increased at 20W after a decrease in pulmonary capillary wedge pressure. These findings have important clinical implications and indicate that lowering pulmonary capillary wedge pressure does not decrease dyspnea on exertion in patients with HFpEF; rather, lowering pulmonary capillary wedge pressure exacerbates dyspnea on exertion, increases V˙/Q˙ mismatch, and worsens ventilatory efficiency during exercise in these patients. This study provides compelling evidence that high pulmonary capillary wedge pressure is likely a secondary phenomenon rather than a primary cause of dyspnea on exertion in patients with HFpEF, and a new therapeutic paradigm is needed to improve symptoms of dyspnea on exertion in these patients.

Double-decker-shaped phenyl-substituted silsesquioxane (DDSQ)-based nanocomposite polyimide membranes with tunable gas permeability and good aging resistance

Membrane-based gas separation technique shows great potential in CO2 elimination from natural gas and N2 enrichment from compressed air. In this study, a double-decker-shaped phenyl-substituted silsesquioxane (DDSQ)-based diamine monomer, that is, DDSQ-diamine, was synthesized and subsequently copolymerized with 4,4′-(hexafluoroisopropylidene) diphthalic anhydride (6FDA) in combination with 4,4′-oxydianiline (ODA) to fabricate a series of DDSQ-based polyimide membranes with intrinsic microporosity (PIM-PIs). The resulting membranes showcase desirable mechanical robustness, satisfactory heat resistance and good organo solubility. Owing to the inherent internal nanometer-sized cavity of DDSQ cage, DDSQ-based membranes are more nanoporous than DDSQ-free sample, accordingly exhibiting decreasing membrane density and increasing gas permeability. Among all membranes, DDSQ-25 and DDSQ-50 show more desirable overall gas separation performance, which almost achieve the 1991 Robeson upper bound. Additionally, DDSQ-25 demonstrates good plasticization resistance and CO2/CH4 mixed-gas separation properties when measured with 50:50 CO2/CH4 binary gas mixture at upstream pressure up to 20 bar. Despite physical aging at ambient conditions for 300 days, the resultant DDSQ-based polyimide membranes still have stable gas permeability and almost constant selectivity, showcasing satisfactory anti-aging characteristic.

The neglected autoxidation pathways for the formation of highly oxygenated organic molecules (HOMs) and the nucleation of the HOMs generated by limonene

Recent ambient atmospheric measurements have observed highly oxygenated organic molecules (HOMs) at a number of sites. Monoterpenes, in particular, are inclined to autoxidize to form HOMs with different oxidants such as OH and O3. However, little is known about the formation and nucleation of the HOMs in the presence of water (W). In this study, we investigated oxidation mechanism of O3 addition to limonene in the gas and water phase by theoretical chemistry calculations. Besides, the mechanism of the formation of HOMs from photochemical reactions of limonene and the role of HOMs in new particle formation (NPF) with aerosol nucleation precursors, including sulfuric acid (SA), W and ions were investigated by means of molecular dynamics (MD) simulations and theoretical chemistry calculations. The rate constants of initiation reactions for O3 addition to limonene are suppressed as the temperature increases. In the process of ion-induced nucleation, HOMs can dominate the initial nucleation steps. The MD results indicated that HOMs can self-aggregate into clusters and W molecules are beneficial to promote the NPF of HOMs. In addition, the nucleation ability of HOMs have significant correlation with the oxygen-to-carbon (O/C) ratio of HOMs. The theoretical results proved the neglected autoxidation pathways including (i) the formation of an endoperoxide moiety in HOMs (ii) a CO2 elimination in presence of an unsaturated peroxy acyl radical. The current study provide valuable insight into NPF mechanism of (HOMs) (SA) and (HOMs) (ion) in the presence of W.

Development of a Novel Infant Volumetric Capnography Simulator: Making the Invisible Visible Improves Understanding and Safety.

Volumetric capnography depicts volumetric capnograms [ie, the plot of expired carbon dioxide (CO 2 ) over the tidal volume]. This bench study aimed to determine the reliability, accuracy, and precision of a novel infant simulator for volumetric capnography. This simulator would be clinically valuable for teaching purposes because it reflects the entire cardiopulmonary physiology within 1 breath. An infant lung simulator was fed with CO 2 supplied by a mass flow controller (VCO 2-IN ) and ventilated using standard settings. A volumetric capnograph was placed between the endotracheal tube and the ventilatory circuit. We simulated ventilated babies of different body weights (2, 2.5, 3, and 5 kg) with a VCO 2 ranging from 12 to 30 mL/min. The correlation coefficient ( r2 ), bias, coefficient of variation (CV = SD/ x × 100), and precision (2 × CV) between the VCO 2-IN and the elimination of CO 2 recorded by the capnograph (VCO 2-OUT ) were calculated. The quality of the capnogram's waveforms was compared with real ones belonging to anesthetized infants using an 8-point scoring system, where 6 points or greater meant that the simulated capnogram showed good, 5 to 3 points acceptable, and less than 3 points an unacceptable shape. The correlation between VCO 2-IN and VCO 2-OUT was r2 = 0.9953 ( P < 0.001), with a bias of 0.16 (95% confidence intervals from 0.12 to 0.20) mL/min. The CV was 5% or less and the precision was 10% or less. All simulated capnograms showed similar shapes compared with real babies, scoring 6 points for 3 kg and 6.5 points for 2-, 2.5-, and 5-kg babies. The simulator of volumetric capnograms was reliable, accurate, and precise for simulating the CO 2 kinetics of ventilated infants.

Health effects of filtering facepiece respirators: Systematic review of pulmonary and cardiovascular effects.

Filtering facepiece respirators (FFRs) were introduced to protect the wearer by removing small particles from inspired air. FFRs are now also used to reduce the spread of transmissible agents from the wearer and are worn outside traditional healthcare and other workplaces. The COVID-19 pandemic increased concerns about potential adverse effects on wearers. A PUBMED query retrieved articles through June 2022. Abstracts and selected full-text articles were systematically reviewed by the authors. This article focuses upon cardiopulmonary physiologic effects (e.g., ventilation, CO2 elimination, oxygen uptake, and respiratory control) with emphasis upon current and potential research methods as well as summarizing results. 1985 records were identified, of which only 26% were published before 2020. FFR effects on CO2 elimination appear more likely to be significant than effects on oxygenation or cardiovascular function. While FFRs appear well tolerated by healthy persons, more research is needed for those with pulmonary or cardiac disorders, and for children. Many traditional pulmonary exercise study methods require special care when applied to filtering facepiece respirators. Studying additional parameters may explain the paradox of many subjective discomfort reports despite very limited physiologic effects.

Ethylcarbene versus Direct Propene Formation in the Near-UV Photodissociation of Ethylketene

The competing pathways in the photodissociation of gaseous ethylketene at excitation wavelengths of 320.0, 340.0, and 355.1 nm were studied using photofragment translational energy spectroscopy. The primary dissociation channel was C═C bond fission producing ethylcarbene (CH3CH2CH; also known as propylidene) and CO. Product translational energy distributions are consistent with theoretical predictions that ground state ethylcarbene lies ∼34 kJ/mol higher in energy than its isomer dimethylcarbene (CH3CCH3). A second dissociation channel involved direct formation of propene prior to or concurrent with CO elimination. The measured product branching ratios indicate that the effective potential energy barrier for the direct propene channel lies below the energetic threshold for ethylcarbene formation. A minor C-C bond fission channel was also observed, leading to CH3 + CH2CHCO products. Comparisons are made to the results of our recent studies of methylketene and dimethylketene photodissociation.

Insertion of CO2 and CS2 into Bi-N bonds enables catalyzed CH-activation and light-induced bismuthinidene transfer.

The uptake and release of small molecules continue to be challenging tasks of utmost importance in synthetic chemistry. The combination of such small molecule activation with subsequent transformations to generate unusual reactivity patterns opens up new prospects for this field of research. Here, we report the reaction of CO2 and CS2 with cationic bismuth(iii) amides. CO2-uptake gives isolable, but metastable compounds, which upon release of CO2 undergo CH activation. These transformations could be transferred to the catalytic regime, which formally corresponds to a CO2-catalyzed CH activation. The CS2-insertion products are thermally stable, but undergo a highly selective reductive elimination under photochemical conditions to give benzothiazolethiones. The low-valent inorganic product of this reaction, Bi(i)OTf, could be trapped, showcasing the first example of light-induced bismuthinidene transfer.