The Influencing Factors for Volume Stability of Ladle Slag

The purpose of this study was to investigate the mechanism causing the unsoundness of ladle slag. Calcination temperature may have an impact on the level of reactivity of f-CaO. When CaO was produced at a higher temperature, the reactivity of CaO was lower. For example, dead burnt CaO (DCaO) was produced at higher temperatures than light burnt CaO (LCaO); therefore, DCaO had less reactivity than LCaO. In a hydration test, DCaO (1500 °C) showed 62 times lower reactivity than LCaO (900 °C), which meant that DCaO would result in the delay of hydration of CaO easily. Additionally, DCaO would cause unsoundness more easily than LCaO when adding the same number of cementitious materials. For this reason, using ASTM C114-18 (Standard Test Methods for Chemical Analysis of Hydraulic Cement) to quantify DCaO content may underestimate DCaO content by up to 20%. Conversely, this method was more suitable for f-CaO since it had high reactivity. Moreover, this study demonstrated that ladle slag would cause unsoundness when added into the cementitious material because it was produced from a higher temperature process (over 1500 °C), which generates the DCaO. Therefore, when reusing ladle slag, the problem of low reactivity of DCaO should be considered.

Effect of Pyrolysis Atmosphere on the Gasification of Waste Tire Char

The aim of the study is to assess the influence of the atmosphere during pyrolysis on the course of CO2 gasification of a tire waste char. Two approaches were used: the pyrolysis step was carried out in an inert atmosphere of argon (I) or in an atmosphere of carbon dioxide (II). The examinations were carried out in non-isothermal conditions using a Rubotherm DynTherm thermobalance in the temperature range of 20–1100 °C and three heating rates: 5, 10 and 15 K/min. Based on the results of the gasification examinations, the TG (Thermogravimetry) and DTG (Derivative Thermogravimetry) curves were developed and the kinetic parameters were calculated using the KAS (Kissinger-Akahira-Sunose) and FWO (Flynn-Wall-Ozawa) methods. Additionally, the CO2 gasification of tire chars reaction order (n), was evaluated, and the kinetic parameters were calculated with the use of Coats and Redfern method. Tire waste char obtained in an argon atmosphere was characterized by lower reactivity, which was reflected in shift of conversion and DTG curves to higher temperatures and higher mean values of activation energy. A variability of activation energy values with the progress of the reaction was observed. For char obtained in an argon atmosphere, the activation energy varied in the range of 191.1–277.2 kJ/mol and, for a char obtained in an atmosphere of CO2, in the range of 148.0–284.8 kJ/mol. The highest activation energy values were observed at the beginning of the gasification process and the lowest for the conversion degree 0.5–0.7.

Temporal Patterns of Daily Behavioral and Psychological Symptoms of Dementia Throughout the Day

Behavioral and psychological symptoms of dementia (BPSD) are taxing for both the person with dementia (PWD) and their family caregivers. Yet, little is known about how BPSD fluctuates throughout the day (i.e., morning, daytime, evening, and night; e.g., sundowning) and how caregivers perceive BPSD at different times of the day. Using 8-day daily diary data from 173 family caregivers whose relatives were using Adult Day Services (ADS), this study investigated temporal patterns of BPSD and caregivers’ stress responses to BPSD throughout the day. Overall, the number of BPSD was highest in the evening, and caregivers’ stress reactivity to BPSD increased throughout the phases of the day (i.e., most stressful at night). However, caregivers showed lower reactivity to BPSD in the mornings and at night on days when the PWD used ADS. Our findings about fluctuations of (caregiver reactions to) BPSD throughout the day suggest target windows for just-in-time adaptive intervention.

Non-Formaldehyde, Bio-Based Adhesives for Use in Wood-Based Panel Manufacturing Industry—A Review

There is a strong need to develop and implement appropriate alternatives to replace formaldehyde-based adhesive systems, such as phenol–formaldehyde, in the industry of wood-based panels (WBPs). This is due to the toxicity and volatility of formaldehyde and restrictions on its use associated with some formaldehyde-based adhesives. Additionally, the current pressure to reduce the dependence on polymeric materials, including adhesives, from petrochemical-based sources has led to increased interest in bio-based adhesives, which, in some cases, already provide acceptable properties to the end-product. Among the potential raw materials for good-quality, renewable-based adhesive formulations, this paper highlights tannins, lignin, and protein sources. However, regarding renewable sources, specific features must be considered, such as their lower reactivity than certain petrochemical-based sources and, therefore, higher production costs, resource availability issues, and the need for toxicological investigations on alternative systems, to compare them to conventional systems. As a result, further research is highly encouraged to develop viable formaldehyde-free adhesive systems based on renewable sources, either at the technical or economical level. Moreover, herein, we also showcase the present market of WBPs, highlighting the obstacles that the alternative and new bio-based adhesives must overcome.

Exploring the Effects of Piston Bowl Geometry and Injector Included Angle On Dual-Fuel and Single-Fuel RCCI

Reactivity Control Compression Ignition (RCCI) is a Low-Temperature Combustion (LTC) technique that have been proposed to meet the current demand for high thermal efficiency and low engine-out emissions. However, its requirement of two separate fuel systems has been one of its major challenges in the last decade. This leads to the single-fuel RCCI concept, where the secondary fuel is generated from the primary fuel through CPOX reformation. After studying three different fuels, diesel was found to be the best candidate for the reformation process, where the reformed gaseous fuel (with lower reactivity) was used as the secondary fuel and the parent diesel fuel (with higher reactivity) was used as the primary fuel. Previously, the effects of the start of injection (SOI) timing of diesel and the energy-based blend ratio were studied in detail. In this study, the effect of piston profile and the injector included angles were experimentally studied using both conventional fuel pairs and reformate RCCI. A validated CFD model was also used for a better understanding of the experimental trends. Comparing a re-entrant bowl piston with a shallow bowl piston, the latter showed better thermal efficiency, regardless of the fuel combination, due to its 10% lower surface area for the heat transfer. Comparing the 150-degree and 60-degree included angle, the latter showed better combustion efficiency, regardless of the fuel combination, due to its earlier combustion phasing (at constant SOI timing) as the fuel spray targets better region of the cylinder.

Cobalt-Mediated Radical Copolymerization of Vinylidene Fluoride and 2,3,3,3-Trifluoroprop-1-ene

New copolymers based on vinylidene fluoride (VDF) and 2,3,3,3-tetrafluoroprop-1-ene (1234yf) were synthesized by organometallic-mediated radical copolymerization (OMRcP) using the combination of bis(tert-butylcyclohexyl) peroxydicarbonate initiator and bis(acetylacetonato)cobalt(II), (Co(acac)2) as a controlling agent. Kinetics studies of the copolymerization of the fluoroalkenes copolymers were monitored by GPC and 19F NMR with molar masses up to 12,200 g/mol and dispersities (Đ) ranging from 1.33 to 1.47. Such an OMRcP behaves as a controlled copolymerization, evidenced by the molar mass of the resulting copolymer-monomer conversion linear relationship. The reactivity ratios, ri, of both comonomers were determined by using the Fineman-Ross and Kelen-Tüdos fitting model leading to rVDF = 0.384 ± 0.013 and r1234yf = 2.147 ± 0.129 at 60 °C, showing that a lower reactivity of VDF integrated in the copolymer to a greater extent leads to the production of gradient or pseudo-diblock copolymers. In addition, the Q (0.03) and e (0.06 and 0.94) parameters were assessed, as well as the dyad statistic distributions and mean square sequence lengths of PVDF and P1234yf.

Antithrombin resistance rescues clotting defect of homozygous prothrombin-Tyr510N dysprothrombinemia

A patient with hematuria in our clinic was diagnosed with urolithiasis. Analysis of the patient’s plasma clotting-time indicated that both APTT (52.6 s) and PT (19.4 s) are prolonged and prothrombin activity is reduced to 12.4% of normal, though the patient exhibited no abnormal bleeding phenotype and a prothrombin antigen level of 87.9%. Genetic analysis revealed the patient is homozygous for prothrombin Y510N mutation. We expressed and characterized the prothrombin-Y510N variant in appropriate coagulation assays and found that the specificity constant for activation of the mutant zymogen by factor Xa is impaired ~5-fold. Thrombin generation assay using patient’s plasma and prothrombin-deficient plasma supplemented with either wild-type or prothrombin-Y510N revealed that both peak height and time to peak for the prothrombin mutant are decreased however the endogenous thrombin generation potential is increased. Further analysis indicated that the thrombin mutant exhibits resistance to antithrombin and is inhibited by the serpin with ~12-fold slower rate constant. Protein C activation by thrombin-Y510N was also decreased ~10-fold, however, thrombomodulin overcame the catalytic defect. The Na+-concentration-dependence of the amidolytic activities revealed that the dissociation constant for the interaction of Na+ with the mutant has been elevated ~20-fold. These results suggest that Y510 (Y184a in chymotrypsin numbering) belongs to network of residues involved in binding Na+. A normal protein C activation by thrombin-Y510N suggests that thrombomodulin modulates the conformation of the Na+-binding loop of thrombin. The clotting defect of thrombin-Y510N appears to be compensated by its markedly lower reactivity with antithrombin, explaining patient’s normal hemostatic phenotype.

Influences of C5 esters addition on anti-knock and auto-ignition tendency of a gasoline surrogate fuel

The research octane numbers and auto-ignition characteristics of a toluene primary reference fuel (TPRF), when blended with three C5 esters, γ-valerolactone (GVL), methyl butanoate (MB), and methyl crotonate (MC), were investigated on a cooperative fuel research (CFR) engine and a constant volume combustion chamber (CVCC). In fuel preparation, ethanol was used to improve the miscibility, and the total additive comprised 1/3 ethanol and 2/3 GVL/MB/MC on a molar basis. The experimental results first reveal that the addition of the three series of additives boost fuel octane rating, and their boosting effects rank as MB > GVL ∼ MC when fuels are blended on a molar basis. In contrast, the auto-ignition tendency of the three series of fuel blends, when blended on the molar basis, ranks as the MC blends > the GVL blends> the MB blends. Different from the similar reactivities observed for the MC blends and the GVL blends in the RON tests, the MC blends exhibit higher auto-ignition propensity than the GVL blends, probably because the higher enthalpy of vaporization of GVL causes a more significant cooling effect. Finally, different from the literature studies that reported similar reactivities for pure MB and MC, in this study MB shows lower reactivity than MC when blending with the TPRF gasoline surrogate.

Enantioselective Conjugate Addition of Catalytically Generated Zinc Homoenolate

<div> <div> <div> <p>We report herein an enantioselective conjugate addition reaction of a zinc homoenolate, catalytically generated via ring opening of a cyclopropanol, to an α,β-unsaturated ketone. The reaction is promoted by a zinc aminoalkoxide catalyst generated from Et2Zn and a chiral β-amino alcohol to afford 1,6- diketones, which undergo, upon heating, intramolecular aldol condensation to furnish highly substituted cyclopentene derivatives with good to high enantioselectivities. The reaction has proved applicable to various 1-substituted cyclopropanols as well as chalcones and related enones. The chiral amino alcohol has proved to enable ligand-accelerated catalysis of the homoenolate generation and its conjugate addition. Positive nonlinear effects and lower reactivity of a racemic catalyst have been observed, which can be attributed to a stable and inactive heterochiral zinc aminoalkoxide dimer. </p> </div> </div> </div>

Enantioselective Conjugate Addition of Catalytically Generated Zinc Homoenolate

<div> <div> <div> <p>We report herein an enantioselective conjugate addition reaction of a zinc homoenolate, catalytically generated via ring opening of a cyclopropanol, to an α,β-unsaturated ketone. The reaction is promoted by a zinc aminoalkoxide catalyst generated from Et2Zn and a chiral β-amino alcohol to afford 1,6- diketones, which undergo, upon heating, intramolecular aldol condensation to furnish highly substituted cyclopentene derivatives with good to high enantioselectivities. The reaction has proved applicable to various 1-substituted cyclopropanols as well as chalcones and related enones. The chiral amino alcohol has proved to enable ligand-accelerated catalysis of the homoenolate generation and its conjugate addition. Positive nonlinear effects and lower reactivity of a racemic catalyst have been observed, which can be attributed to a stable and inactive heterochiral zinc aminoalkoxide dimer. </p> </div> </div> </div>