Kinetic Method Research Articles

A-125 Difference Between the Results of Vitros® Dry Biochemistry and Wet Biochemistry with Kinetic Method in Diagnosing the Comorbidity of Lung Adenocarcinoma and Aacroamylasemia: Case Report

Abstract Background Amylase (AMY) is a biomarker that comes mainly from the pancreas and salivary glands. Macroamylasemia is a condition often accompanied by malignant tumors and clinical features that include: (i) recurrent abdominal pain, no abnormality in the salivary glands, serum amylase (AMY) level ≥2 to 3 times higher than the normal value and poor patient response to treatments for pancreatitis; (ii) normal serum creatinine and urea levels, increased serum AMY level, and urine AMY level within the normal range or slightly lower. Because macroamylasemia may cause abnormally increased serum AMY levels for a long period of time, misdiagnosis of pancreatitis and delayed diagnosis/treatment of the disease may occur. We report a case of lung adenocarcinoma with macroamylasemia that was co-diagnosed using wet chemistry with kinetic method and dry chemistry to measure AMY. Methods A 47-year-old male patient was previously diagnosed with “acute pancreatitis and lung infection” after initial admission to a local hospital with paroxysmal cough and abdominal pain without obvious cause. To further diagnose the patient, we determined the blood AMY level by using the wet chemistry with kinetic method and the Vitros® dry chemistry test, in addition to conducting a physical exam, abdominal and chest computed tomography (CT), and other lab tests. Two methods, calculation of amylase/creatinine clearance ratio (Cam/Ccr ratio) and protein precipitation by polyethylene glycol (PEG), were also performed to validate assumed interference by serum macroamylase (MAMS) in the wet chemistry method compared to the dry chemistry method, which has technology to capture large molecules and minimize the impact of interferents. MAMS is a high-molecular-weight AMY complex that is synthesized by normal serum AMY bound with macromolecular substances (eg, immunoglobulins and carbohydrates). Results The final diagnosis was a stage IIB cT3N0M0 adenocarcinoma of the upper lobe of the right lung and macroamylasemia. Symptoms and radiologic findings were atypical in terms of pancreatitis. Serum AMY was 2,178U/L when measured with the wet chemistry with kinetic method. When the specimen was re-tested with Vitros dry chemistry, the AMY level was 369 U/L. After precipitation with 25% PEG 6000 solution, the blood AMY level from wet chemistry decreased from 2395.1 U/L to 246.7 U/L, yielding a precipitation rate of 89.7%. Cam/Ccr ratio was calculated as 0.23% (<1%). The calculated PEG precipitation rate and Cam/Ccr ratio from this study were consistent with the ranges considered for macroamylasemia, which are ≥73% and Cam/Ccr ratio <1%, respectively. Conclusions High serum AMY levels do not necessarily indicate pancreatitis or parotitis; wet chemistry results can be impacted by the presence of serum macroamylase. Instead of relying solely on blood AMY in diagnosing acute pancreatitis, clinicians should also consider the correlations of blood AMY with urine AMY and blood lipase. In patients with prolonged blood AMY elevation but normal lipase and urine AMY, re-testing of AMY with a more interference-resistant methodology (e.g. Vitros dry chemistry) may be requested. Accordingly, Cam/Ccr ratio calculation and PEG precipitation can be performed to validate the diagnosis of macroamylasemia.

A-232 Characterize and reduce positive interference of hemolysis on Fungitell testing for (1, 3)-β-glucan (BDG) in serum

Abstract Background Fungitell is an FDA cleared in vitro diagnostic product with an indication for use as an adjunct test for the diagnosis of invasive fungal infection. This assay has been established using a kinetic photometric method. A key aspect of this (1→3)-β-glucan (BDG) activated cascade reaction is its characteristic kinetic optical density profile. Interference which affects the BDG kinetic profile makes data analysis and interpretation difficult. This interference is roughly classified as being associated with hemolysis, icterus, lipemia (collectively HIL), and other non-specific factors. Methods In this study, we found that the use of 5% PEG-8000 supplemented serum (1:1 ratio of the volume of serum to 10% PEG-8000 solution with 0.1 M Tris-Cl, pH 7.4), heated at 80°C for 3.5 min, followed by centrifugation at 15,000 x g for 10 minutes (PEG-X Method) can largely eliminate the hemolysis-associated interference. Results The treated serum Fungitell BDG reaction curves are more like the ideal BDG kinetic profile. The recovery of introduced β-glucan has been shown to be acceptable (80-120%) for hemolyzed specimens. Conclusions This simple and rapid procedure shows promise as a pre-analytical treatment to reduce serum interference in the Fungitell β-glucan test for a substantial fraction of samples that produce currently unreportable results.

A-318 Validation of umbilical cord blood as an alternate sample type for quantitative in vitro detection of glucose-6-phosphate dehydrogenase in neonates

Abstract Background Detection of glucose-6-phosphate dehydrogenase (G6PD) deficiency provides important information for neonatal clinical management. G6PD newborn screening is recommended using umbilical cord blood specimens in vulnerable patient populations.1 Also, cord blood is used by many clinicians instead of peripheral blood for neonatal screening of G6PD.2 Use of cord blood is a modification to the FDA-approved Pointe Scientific G6PD kinetic-340 nm assay. The aim of this study was to validate cord blood as an alternate specimen type for the Pointe Scientific G6PD assay. Methods Hemoglobin (Hgb) results are from Sysmex XN 9100™ analyzers that use SLS methodology with photometric detection. G6PD results are from Roche cobas® c502 analyzers with Pointe Scientific kinetic method and spectrophotometric detection of activity, expressed as U/g Hgb. Neonatal blood specimens were obtained as paired samples from heel sticks and umbilical cord collected in EDTA lavender top tubes. Accuracy acceptance criteria was defined as Deming regression slope between 0.90 and 1.10, r-value of >0.90 and bias ±15% and mixing study recovery of ±10%. Precision (intra-assay and inter-assay), reportable range and linearity, carryover, and stability were established using cord blood samples or control materials sourced from Thermo Fisher Scientific or Sysmex. Reference intervals3, analytical sensitivity, specificity, and clinical validity were transferred to cord blood due to comparability with whole blood FDA-approved method. EP Evaluator software by Data Innovations® was used for calculations. Results Direct comparison of G6PD results (U/g Hgb) from 125 paired samples yielded a 0.9025 correlation coefficient, 1.024 Deming slope, and -0.25% bias. Mixing and recovery of admixed samples gave % recoveries of 102, 103, 101, 102, 100, and 100 for G6PD (U/g Hgb), and 102, 102, 101, 104, 99, and 105 for Hgb (g/dL). Intra-assay precision results were 2.4, 0.6, 0.8, 0.5, 0.4 % CV for G6PD and Hgb, respectively. Inter-assay precision results were 3.1, 3.3, 0.7, 0.7, 0.5 % CV for G6PD and Hgb, respectively. Reportable range and linearity evaluation resulted in a maximum deviation from target recovery of 4%, and a slope of 0.979 for a range of 50 - 2740 U/L, and reportable range for Hgb was confirmed as 0.1 - 26.0 g/dL using controls (1% maximum deviation and 0.991 slope). Carryover was -5.8 (mean concentration) for G6PD and 0% for Hgb after testing 21 replicates of pooled high and low samples in a defined order. Testing 3 samples in 3 replicates at each defined time interval defined stability as 1 week refrigerated or 72 hours room temperature for G6PD, and 3 days refrigerated or 1 day room temperature for Hgb. Conclusions Regression statistics and mixing-recovery studies demonstrated accuracy for detecting G6PD (U/g Hgb) and Hgb (g/dL) from EDTA cord blood. Additional performance characteristics were transferrable for this specimen type from the FDA-approved method for whole blood. Umbilical cord blood is an acceptable alternate specimen type for quantitative detection of G6PD (U/g Hgb) using Pointe Scientific with Sysmex XN-9100™ and Roche cobas® c502 instrumentation.

A brigde toward mathematics theory in living systems: the thermostatted kinetic theory method for crowd dynamics: Comment on the review paper “A decade of thermostatted kinetic theory models for complex active matter living systems” by Carlo Bianca

A brigde toward mathematics theory in living systems: the thermostatted kinetic theory method for crowd dynamics: Comment on the review paper “A decade of thermostatted kinetic theory models for complex active matter living systems” by Carlo Bianca

Monomeric and Dimeric Boron (III) Subphthalocyanines Functionalized with 4-Hydroxy-Benzoic Acid as Potential Photosensitizers and Photocatalysts in Sulfoxidation.

Axial modification of boron (III) subphthalocyanine bromides with 4-hydroxy-benzoic acid successfully led to the formation of the macrocycles with anchored 4-carboxyphenoxy group [RsPcPHBA] (R=tBu, H) in the axial position and to a new dimer [sPcPHBAsPc] as minor product. Tri-tert-butyl and unsubstituted subphthalocyanines bearing benzoate ([tBusPcBA], [sPcBA]), phenoxy-group ([tBusPcOPh], [sPcOPh])) in the axial position, have been also investigated as well as control sPcs. All compounds were characterized by NMR, IR, UV-Vis and mass spectrometry. The electrochemical properties were studied using cyclic voltammetry (CV) and square wave voltammetry (SWV). Singlet oxygen generation was systematically measured for all synthesized [RsPcX] by kinetic method of chemical trap decomposition (DPBF) and by determination of phosphorescence of singlet oxygen (at 1270 nm). Axially modified subphthalocyanines exhibit high quantum yields of singlet oxygen (1O2) generation (0.47-0.62). The observed exceptional photostability in oxygen-saturated ethanol or toluene solutions and high 1O2 quantum yields allows to use [tBusPcPHBA] as photocatalysts of selective oxidative transformations of organic sulfides to sulfoxides. Loading the catalyst to 9.7 ⋅ 10-2 mol % made it possible to achieve complete conversion of the substrate (TON up to 1700).

Modified creatinine index as a marker of skeletal muscle mass in peritoneal dialysis patients.

Sarcopenia is common in peritoneal dialysis (PD) patients. Modified creatinine index (MCrI) by the Canaud's formula and single-pool Kt/V value is an accurate surrogate marker for muscle mass in hemodialysis patients. However, the method of calculation and validity of MCrI has not been tested in PD. In the exploratory cohort, we studied 138 consecutive patients converted from PD to hemodialysis. Their MCrI during PD, calculated by the Canaud's formula with total weekly Kt/V, and the conventional MCrI after conversion to HD, were compared by the Bland-Altman method. Their correlation with muscle mass as determined by bioimpedance spectroscopy and creatinine kinetic methods was explored. The result was then validated in a second cohort of 605 incident PD patients. In the exploratory cohort, the average bias of computing MCrI during PD and hemodialysis was 0.758mg/kg/day (95%CI -4.356 to 5.873mg/kg/day). The MCrI during PD significantly correlated with the muscle mass by creatinine kinetics (r=.684, P<.0001) and by bioimpedance spectroscopy (r=.641, P<.0001), but not with protein nitrogen appearance, overhydration, or adipose tissue mass, and the result was similar in the validation cohort. For incident PD patients, MCrI quartile was significantly associated with the risk of death from all cause in 12 months (Gray's test, P=.013) but not conversion to chronic hemodialysis (P=.14). In PD patients, MCrI computed by the Canaud's formula and total weekly Kt/V is a simple and reliable marker of skeletal muscle mass and may serve as a short-term prognostic indicator.

Thermomechanical Properties of Ramie Fiber/Degradable Epoxy Resin Composites and Their Performance on Cylinder Inner Lining.

Type IV gas cylinders are widely used in the field of vehicles due to their advantages such as light weight, cleanliness, and low cost. Ramie fiber/degradable epoxy resin composites (RFRDE) provide new ideas for the material selection of Type IV gas cylinders due to their advantages of low carbon emissions, low environmental pollution, and renewable resource utilization. However, the poor interfacial bonding strength and moisture resistance between polyethylene plastics and RFRDE have limited their application areas. This study tested the mechanical properties of ramie fibers at different heat treatment temperatures, and studied the thermal mechanical properties of RFRDE through differential scanning calorimeter and curing kinetics methods. At 180 °C, the tensile strength of fiber bundles decreased by 34% compared to untreated fibers. As the highest curing temperature decreases, the tensile strength of RFRDE increases but the curing degree decreases. At the highest curing temperature of 100 °C, the tensile strength of RFRDE is 296 MPa. The effect of the corona discharge and flexible adhesive on the surface modification of polyethylene was analyzed using scanning electron microscopy. These results provide guidance for the development of natural fiber/degradable epoxy resin composite materials.

Rationalize the Functional Roles of Protein-Protein Interactions in Targeted Protein Degradation by Kinetic Monte-Carlo Simulations.

Targeted protein degradation is a promising therapeutic strategy to tackle disease-causing proteins that lack binding pockets for traditional small-molecule inhibitors. Its first step is to trigger the proximity between a ubiquitin ligase complex and a target protein through a heterobifunctional molecule, such as proteolysis targeting chimeras (PROTACs), leading to the formation of a ternary complex. The properties of protein-protein interactions play an important regulatory role during this process, which can be reflected by binding cooperativity. Unfortunately, although computer-aided drug design has become a cornerstone of modern drug development, the endeavor to model targeted protein degradation is still in its infancy. The development of computational tools to understand the impacts of protein-protein interactions on targeted protein degradation, therefore, is highly demanded. To reach this goal, we constructed a non-redundant structural benchmark of the most updated ternary complexes and applied a kinetic Monte-Carlo method to simulate the association between ligases and PROTAC-targeted proteins in the benchmark. Our results show that proteins in most complexes with positive cooperativity tend to associate into native-like configurations more often. In contrast, proteins very likely failed to associate into native-like configurations in complexes with negative cooperativity. Moreover, we compared the protein-protein association through different interfaces generated from molecular docking. The native-like binding interface shows a higher association probability than all the other alternative interfaces only in the complex with positive cooperativity. These observations support the idea that the formation of ternary complexes is closely regulated by the binary interactions between proteins. Finally, we applied our method to cyclin-dependent kinases 4 and 6 (CDK4/6). We found that their interactions with the ligase are not as similar as their structures. Altogether, our study paves the way for understanding the role of protein-protein interactions in PROTACE-induced ternary complex formation. It can potentially help in searching for degraders that selectively target specific proteins.

Unveiling the impact of nitrocellulose-enveloped nCuO on the thermal characteristics of ammonium nitrate-based solid composite propellants utilizing polyurethane/nitrocellulose blend binders

ABSTRACT This study investigates the combined effects of coated nano copper oxide (NC@nCuO) and polyurethane (PU) modification on the thermal degradation kinetics and combustion properties of ammonium nitrate-based solid composite propellant. Nitrocellulose (NC) is used as a coating for nCuO, forming a core-shell structure, and as a binder in a PU/NC blend. Surface modification of ammonium nitrate was achieved through repeated spray coating. The formulations underwent thorough thermal characterization using thermogravimetry (TG) and differential scanning calorimetry (DSC) analyses. TG analysis showed a significant decrease in thermal degradation temperature due to AN modification with NC@nCuO and the use of PU/NC as a binder. Isoconversional kinetic methods (it-KAS, it-FWO, and VYA/CE) based on DSC tests were used to predict kinetic parameters, revealing a substantial impact of NC-coated nCuO and PU modification on the reactivity of the propellant, reducing the activation energy from 125 kJ/mol (reference) to 99 kJ/mol (nCuO) and 94 kJ/mol (NC@nCuO). Additionally, combustion tests were conducted. The results showed that the introduction of nCuO reduces the ignition delay by 5.25 ms and the combustion duration by 0.06 ms, while NC@nCuO further reduces these by 8.17 ms and 0.12 ms, respectively. Additionally, there is a 23% and 65% increase in flame intensity relative to the reference formulation after the incorporation of nCuO and NC@nCuO, repectively.

A Benchmark for Neutron Kinetics Methods in Hexagonal Geometry

A new benchmark solution has been developed to aid in the development of neutron kinetics solvers for hexagonal geometries, such as those in water-water energetic reactors. This benchmark problem is based on the two-dimensional, two-group, International Atomic Energy Agency–Hex steady-state benchmark problem. Two transient problems are presented: a ramp and a step transient. To create a benchmark-quality solution to this transient problem, a basic neutron kinetics model was added to the computer program LUPINE (Liquid metal–cooled fast reactor Utility for Physics Informed Nuclear Engineering). LUPINE solves neutron kinetics equations in general unstructured mesh. First, the LUPINE kinetics solvers are verified using the TWIGL benchmark problems. Then the methods in LUPINE are used to perform a spatiotemporal convergence analysis to ensure that the solutions are sufficiently converged. Finally, Richardson extrapolation is performed to obtain the reference solutions for these new kinetics benchmark problems.

Study on Explosion Mechanism of Dimethyl Ether/H2-Blended Gas Based on Chemical Kinetics Method

In order to reveal the deflagration mechanism of DME/H2-blended gasses, the micro-mechanism was studied based on the constructed UC San Diego 2016 pyrolysis oxidation mechanism model. The results show that adiabatic flame temperature and laminar flame speed increase with the increase in the equivalence ratio (Φ); they first increase and then decrease with the increase in the hydrogen (H2)-blended ratio (λ), and with the increase in λ, the Φ corresponding to the peak laminar flame speed of the blended gas increases. The addition of H2 increases the consumption of O2, and H2 reacts with CO to form H2O and CO2, promoting complete combustion. When Φ = 1.0–1.2, the equilibrium mole fraction of H and OH-activated radicals reach the maximum, and with the addition of H2, the concentration of activating radicals gradually increases, while the number of promoted elementary reactions increases by two, and the number of inhibited elementary reactions does not increase. Meanwhile, the addition of H2 increases the reaction rate of most reactions on the main chemical reaction path CH3OCH3→CH3OCH2→CH2O→HCO→CO→CO2 of DME and increases the risk of the deflagration of DME/H2-blended gas.

Development of graphene oxide and magnesia immobilized kaolin supported dual biopolymeric hybrid material for methyl orange and malachite green removal from water

Industrial usage of various dyes seriously depends on the efficient treatment of industrial effluents. Efficient retention of waste matter using a variety of adsorbent materials has as a result turned into dangerous. In this research article, graphene oxide (GO) cum magnesium oxide (MgO) impregnated kaolin (KA) based chitosan (CS) and pectin (Pect) composite namely GO/MgO/KA/CS-Pect as an adsorbent material for effective methyl orange (MO) and malachite green (MG) removal in aquatic system. The physico-chemical properties like bonding, structural morphology and elemental composition of GO/MgO/KA/CS-Pect were explored with numerous sophisticated instrumental techniques viz., FTIR, SEM, XRD, EDAX and elemental mapping analysis. The influencing parameters of adsorption method, with effect of reaction time, solution pH, dosage, pHzpc, initial MO/MG concentration and temperature were investigated for MO and MG removal under batch scale. The removal of MO and MG rate of the GO/MgO/KA/CS-Pect was incredibly fast and the adsorption kinetic method was driven with intraparticle diffusion (IPD) and pseudo-second-order (PSO) kinetic models. The adsorption isotherm strongly well-adapted with Langmuir isotherm and the maximum removal efficiency of GO/MgO/KA/CS-Pect was found to be 45.50 and 42.00 mg/g for MO and MG respectively within 40 min. The MO and MG uptake by GO/MgO/KA/CS-Pect was majorly owing to chemical adsorption namely electrostatic adsorption, hydrogen bonding and π-π interaction mechanism. The prepared GO/MgO/KA/CS-Pect was productively regenerated with absolute ethanol and could be repetitively reused. This exploration reveals the feasibility and selectivity of the GO/MgO/KA/CS-Pect as genuine adsorbent material for removal of MO and MG from the aquatic system.

Pyrolysis and Physicochemical, Thermokinetic and Thermodynamic Analyses of Ceiba aesculifolia (Kunth) Britt and Baker Waste to Evaluate Its Bioenergy Potential.

Ceiba aesculifolia is an important species in Mexico that generates significant amounts of biomass waste during its exploitation, which can be utilized to produce energy. This study presents the characterization of this waste based on chemical (proximal and elemental) and thermal analyses (TGA-DTG) at different heating rates (β = 10-30 °C/min (283-303 K/min)) in the presence of nitrogen and in a temperature range of 25-900 °C. Kinetic parameters were calculated and analyzed as well. Activation energy (Ea) and the pre-exponential factor (A) were determined using the Friedman (132.03 kJ/mol, 8.11E + 10 s -1), FWO (121.65 kJ/mol, 4.30E + 09), KAS (118.14 kJ/mol, 2.41E + 09), and Kissinger (155.85 kJ/mol, 3.47E + 11) kinetic methods. Variation in the reaction order, n (0.3937-0.6141), was obtained by Avrami's theory. We also calculated the thermodynamic parameters (ΔH, ΔG, ΔS) for each kinetic method applied. The results for Ea, A, n, ΔH, ΔG, and ΔS show that this biomass waste is apt for use in pyrolysis. Moreover, the moisture (<10%), ash (<2%), volatile material (>80%), and HHV (>19%) contents of C. aesculifolia allowed us to predict acceptable performance in generating energy and fuels. Finally, infrared spectroscopy analysis (FT-IR) allowed us to identify important functional groups, including one that belongs to the family of the aliphatic hydrocarbons.

The Impact of Fractures on Shale Oil and Gas Enrichment and Mobility: A Case Study of the Qingshankou Formation in the Gulong Depression of the Songliao Basin, NE China

To study the impact of faults on the enrichment and mobility of shale oil in the Gulong area, representative rock samples were selected in this paper. Based on geochemical data and chemical kinetics methods, coupled with shale oil enrichment and mobility analysis techniques, the shale oil generation quantity and in situ oil content were evaluated from the perspectives of shale oil generation and micro migration, and the mobility of shale oil was revealed. At the same time, the hydrocarbon expulsion efficiency (HEE) of shale was qualitatively and quantitatively characterized, combined with the development of faults. The research results indicate that the study area mainly develops organic-rich felsic (ORF)/organic-containing felsic (OCF) shale, their proportion in both wells exceeds 65%, and the resource amount is the largest in this type of lithofacies. The development of a fault controls the enrichment of shale oil, and the in situ oil content and oil saturation index (OSI) of the shale in well Y58, which is close to the fault, are significantly worse than those in well S2. Well Y58 has 9.52 mg/g and 424.83 mg/g TOC respectively, while well S2 has 11.34 mg/g and 488.73 mg/g TOC respectively. The fault enhanced the migration of shale oil, increasing the efficiency of oil expulsion. As a result, the components with weak polarity or small molecules, such as saturated hydrocarbons and low carbon number n-alkanes, are prone to migration, reducing the mobility of shale oil.

Estimation of urea, uric acid and creatinine levels in patients of primary hypothyroidism - A cross-sectional study.

The thyroid gland is one of the largest endocrine glands in the body, secreting thyroxine (T4) and triiodothyronine (T3). Mild hypothyroidism can have negative consequences for a variety of tissues, even though clinically the patients are euthyroid. Many research studies were conducted to evaluate the serum creatinine levels of people with hypothyroidism; however, relatively little research was conducted to evaluate serum urea and serum creatinine levels in subclinical hypothyroidism. As a result, the current study was carried out to investigate urea, uric acid, and creatinine levels in hypothyroidism. Our study aimed to determine and correlate the levels of urea, uric acid and creatinine in newly diagnosed primary hypothyroidism cases. In this cross-sectional study, 96 newly diagnosed cases of primary hypothyroidism were included. The findings were correlated with 20-60-year-old and sex-matched cases. Serum urea was determined by the kinetic method (Glutamate Dehydrogenase Method), serum uric acid by the uricase method and serum creatinine by Jaffe's method in Erba's Mannheim fully automated analyser. This study showed a positive correlation between uric acid and thyroid stimulating hormone (TSH) and a negative correlation between urea and creatinine. There was no statistical significance in the mean values of urea, uric acid and creatinine but an increased level of urea, uric acid and creatinine was seen in the age group 20-30 years when compared with the other age groups. The study concludes that serum urea showed a positive correlation with TSH, whereas uric acid and creatinine showed a negative correlation with TSH, and there was no statistical significance in the mean values of urea, uric acid and creatinine in hypothyroid patients.

Kinetic analysis and calculation correction methods for moisture evaporation rate in pine lignocellulosic biomass

This study investigates the kinetics of moisture evaporation in pine wood during the drying stage, focusing on analyzing thermogravimetric (TG) curves. The research is based on the kinetic rate model and TG curves obtained at various heating rates, specifically 5, 10, 15, and 20 K/min for the heat release rate, within a temperature range from room temperature to 473 K. Utilizing thermogravimetric experiments and the kinetic rate model, the apparent activation energy and pre-exponential factor are calculated. Further refinement of these calculations is achieved using the Nelder-Mead algorithm. The results show good agreement between the average values of the apparent activation energy (37.88 kJ/mol) and pre-exponential factor (4458.20 s−1) and experimental measurements in the initial and later drying stages, with discrepancies noted in the middle stage. Establishing a relationship between the correction coefficients of these parameters and the heating rate leads to a reduction in calculation errors. Notably, the pre-exponential factor is found to be influenced by heating rates, while the apparent activation energy remains relatively stable. Moreover, the errors are significantly reduced after correction, and the error curve of 10 K/min is the most significant. Overall, the proposed correction method holds promise for accurately calculating moisture evaporation rates in lignocellulosic biomass, offering valuable insights for biomass drying applications.

A Comparative Study of Cystatin C and Creatinine as a Preliminary Marker of Nephropathy in Type 2 Diabetic Patients

Background: Type 2 diabetes disorder (T2DD) is one of the most common disorder in societies, and its causes are genetic and acquired. This disorder is characterized by an increase in the concentration of glucose in the blood. High concentrations of glucose in the blood for long periods lead to complications, the most important of which is diabetic nephropathy (DNP), which is characterized by the gradual loss of the kidney's filtration function.Material and methods: The present study was designed based on collecting twenty patients with newly DNP (as first group) and twenty healthy individuals (as second group). The levels of HbA1c, Creatinine and Cystatin C of all study individuals were measured using Chromatographic assay method, Kinetic colorimetric method and Immunoturbidimetric assay techniques respectively.Results: This study used the t-test statistical method to compare groups as well as sensitivity and specificity based on HbA1c, creatinine and Cystatin C biomarkers. The current study showed a higher the HbA1c percentage, creatinine level and Cystatin C level in the first group compared to the second group. On the other hand, the current study showed that Cystatin C has greater sensitivity and specificity than creatinine towards the DNP disease.Conclusion: The current study concluded by stating the importance of the role of Cystatin C as an early indicator of DNP disease, as the current study proved that Cystatin C has greater sensitivity and specificity than creatinine towards DNP disease

Thermokinetics and reactive mechanism of lead azide (LA) in atmosphere/temperature mixed environment

To establish the influence of atmospheric and temperature factors on the stability of LA, a combined environmental stress testing device was designed to simulate reaction characteristics. Morphological characterization methods of SEM and FTIR were carried out to explore the changes of crystal structure, as the pyrolysis behavior of LA under the combined environmental stress was investigated by DSC with two isoconversional kinetic methods and thermal safety software (TSS). The research indicates that CO2 and H2O react with LA to generate basic lead carbonate in the air atmosphere, together with the stimulation of thermal stress, the synergistic effect formed microvoids to erode the crystal structure of LA. The microvoid effect reduced the apparent activation energy (Ea) from 156.47 to 29.52 kJ/mol as the order of degradation of thermal stability of LA was Air > N2 > CO2, which demonstrated that CO2 and N2 atmosphere have a particular protective effect for LA storage, transportation, and application. The pyrolysis reaction mechanism model of LA under the combined environment factors testing was the same as the original LA through the calculation of TSS, thereby the findings could contribute to a better understanding of available boundary conditions for LA.

Based on experiment and quantum chemical calculations: a study of the co-pyrolysis mechanism of polyesterimide enameled wires with polyvinyl chloride and the catalytic effect of endogenous metal Cu

Pyrolysis technology is a green and efficient method for recycling enameled wires. However, since waste enameled wires are typically recovered from electronic waste, they often contain small amounts of wires and cables. Therefore, during the pyrolysis process of waste enameled wires, it is inevitable for the paint film and the cable sheath to undergo co-pyrolysis. Polyesterimide enameled wires (EPEsI) and polyvinyl chloride (PVC) were chosen as represent enameled wires and cable sheath materials, respectively. Using thermogravimetric analysis with various pyrolysis kinetic analysis methods, the pyrolysis characteristics and kinetics of EPEsI and Mixture (mixture of EPEsI and PVC) were studied. Through synergy analysis and pyrolysis-gas chromatography/mass spectrometry analysis, the influence of PVC on the pyrolysis of EPEsI was elucidated from aspects such as pyrolysis characteristics and product distribution. Based on density functional theory calculations and wave function analysis, the role of endogenous metal Cu in EPEsI on the pyrolysis processes of PEsI and PVC, as well as the mechanism of HCl from PVC on the pyrolysis of PEsI, were clarified.

A new local and explicit kinetic method for linear and non-linear convection-diffusion problems with finite kinetic speeds: II. Multi-dimensional case

We extend to multi-dimensions the work of [1], where new fully explicit kinetic methods were built for the approximation of linear and non-linear convection-diffusion problems. The fundamental principles from the earlier work are retained: (1) rather than aiming for the desired equations in the strict limit of a vanishing relaxation parameter, as is commonly done in the diffusion limit of kinetic methods, diffusion terms are sought as a first-order correction of this limit in a Chapman-Enskog expansion, (2) introducing a coupling between the conserved variables within the relaxation process by a specifically designed collision matrix makes it possible to systematically match a desired diffusion. Extending this strategy to multi-dimensions cannot, however, be achieved through simple directional splitting, as diffusion is likely to couple space directions with each other, such as with shear viscosity in the Navier-Stokes equations. In this work, we show how rewriting the collision matrix in terms of moments can address this issue, regardless of the number of kinetic waves, while ensuring conservation systematically. This rewriting allows for introducing a new class of kinetic models called regularized models, simplifying the numerical methods and establishing connections with Jin-Xin models. Subsequently, new explicit arbitrary high-order kinetic schemes are formulated and validated on standard two-dimensional cases from the literature. Excellent results are obtained in the simulation of a shock-boundary layer interaction, validating their ability to approximate the Navier-Stokes equations with kinetic speeds obeying nothing but a subcharacteristic condition along with a hyperbolic constraint on the time step.