Reaction Products Research Articles

Study on the Thermal Safety of 3,7‐Dinitro‐1,3,5,7‐Tetraazabicyclo[3.3.1]nonane Synthesized by Nitrolysis of Hexamine

AbstractThe thermal flow curves of the nitrolysis for the synthesis of 3,7‐dinitro‐1,3,5,7‐tetraazabicyclo[3.3.1]nonane (DPT) from hexamine in the presence of different amounts of acetic anhydride were obtained using reaction calorimetry. The maximum heat release rates during the feeding process, the corresponding maximum adiabatic temperature rises, and the Maximum Temperature of the Synthesis Reaction (MTSR) were determined, respectively. The thermal stability of the reaction product DPT and the reaction mixture was analyzed, and data on their thermal decomposition characteristics were obtained. The thermal decomposition kinetic model was utilized to simulate the stability under adiabatic conditions. TD24 (The temperature corresponding to the time required to reach the maximum reaction rate under adiabatic conditions for 24 hours) of the reaction mixture was calculated as 69.65°C. According to the thermal hazard parameters of the reaction, the process's hazard level under various acetic anhydride addition conditions was determined to be level 5 using the cooling failure scenario method.

3D model of a stable triangle LiF–NaBr–KBr four-component reciprocal system Li+, Na+, K+ || F-, Вr-

A 3D model of the phase equilibrium states of the quasi-three-component system LiF–NaBr–KBr, which is a stable triangle of the four-component reciprocal system Li+, Na+, K+ || F-, Br-, has been constructed. Based on the 3D-model, polythermal, isothermal sections and the polytherm of phase crystallization were constructed for the first time. Two polythermal sections contain wide areas of boundary solid solutions based on sodium and potassium bromide. In an isothermal section at 650 оC, the fields of the liquid phase and the coexisting two and three phases are delimited. The crystallization polytherm is represented by three fields. In the crystallization field of lithium fluoride, the area of separation of two liquids is limited. The direction of the ion exchange reaction 2LiBr + NaF + KF = 2LiF + NaBr + KBr was confirmed by thermodynamic calculations at temperatures of 400, 600, 800, 1000K. The exothermic nature of the exchange reaction is confirmed by taking a DTA heating curve for a mixture of powders from 50% LiBr + 25% NaF + 25% KF, and the phase composition of the reaction products LiF + NaBr(OTR) + KBr(OTR) is confirmed by X-ray phase analysis data, where OTR is limited solid solution.

Acceleration of Diffusion in Ab Initio Nanoreactor Molecular Dynamics and Application to Hydrogen Sulfide Oxidation.

The computational description of chemical reactivity can become extremely complex when multiple different reaction products and intermediates come into play, forming a chemical reaction network. Therefore, computational methods for the automated construction of chemical reaction networks have been developed in the last decades. One of these methods, ab initio nanoreactor molecular dynamics (NMD), is based on external forces enhancing reactivity by e.g., periodically compressing the system and allowing it to relax. However, during the relaxation process, a significant simulation time is required to allow energy to dissipate and molecules to diffuse, making this part of the NMD simulation computationally intensive. This work aims to improve NMD by accelerating the diffusion process in the relaxation phase. We systematically investigate the speedup of reaction discovery gained by diffusion acceleration, leading to a factor of up to 28 in discovery frequency. Diffusion-accelerated nanoreactor molecular dynamics (DA-NMD) is then used to construct a reaction network of hydrogen sulfide oxidation under atmospheric conditions, where reactions are automatically detected by a change in the bond order and bond distance. A reaction network of 108 molecular species and 399 elementary reactions was constructed starting from hydrogen sulfide, hydroxy radicals, and molecular oxygen covering a broad variety of sulfur-oxygen chemistry and oxidation states of the sulfur atom ranging from -II to +VI.

An easy and sensitive assay for acetohydroxyacid synthases based on the simultaneous detection of substrates and products in a single step.

Acetohydroxyacid synthase (AHAS, EC 2.2.1.6) catalyzes the first step in the synthesis of the branched-chain amino acids valine, leucine, and isoleucine, pathways being present in plants and microorganisms, but not in animals. Thus, AHAS is an important target for numerous herbicides and, more recently, for the development of antimicrobial agents. The need to develop new and optimized herbicides and pharmaceuticals requires a detailed understanding of the biochemistry of AHAS. AHAS transfers an activated two-carbon moiety derived from pyruvate to either pyruvate or 2-oxobutyrate as acceptor substrates, forming 2-acetolactate or 2-acetohydroxy-2-butyrate, respectively. Various methods have been described in the literature to biochemically characterize AHAS with respect to substrate preferences, substrate specificity, or kinetic parameters. However, the simultaneous detection and quantification of substrates and unstable products of the AHAS-catalyzed reaction have always been a challenge. Using AHAS isoform II from Escherichia coli, we have developed a sensitive assay for AHAS-catalyzed reactions that uses derivatization with ethyl chloroformate to stabilize and volatilize all reactants in the aqueous solution and detect them by gas chromatography coupled to flame ionization detection or mass spectrometry. This assay allows us to characterize the product formation in reactions in single and dual substrate reactions and the substrate specificity of AHAS, and to reinterpret previous biochemical observations. This assay is not limited to the AHAS-catalyzed reactions, but should be applicable to studies of many metabolic pathways.

Structure of METTL3-METTL14 with an m6A nucleotide reveals insights into m6A conversion and sensing.

The nuclear METTL3-METTL14 transfers a methyl group from SAM to convert the N 6 of adenosine (A) in RNA to m 6 A and in ssDNA to 6mA. m 6 A marks are prevalent in eukaryotic mRNAs and lncRNAs and modulate their stability and fate in a context-dependent manner. The cytoplasmic METTL3 can act as a m 6 A reader. However, the precise mechanism during m6A writing, reading, or sensing is unclear. Here, we present a ~2.5 Å structure of the methyltransferase core of human METTL3-METTL14 in complex with the reaction product mimic, N 6 -methyladenosine monophosphate (m 6 A), representing a state post-catalysis but before the release of m 6 A. m 6 A occupies an evolutionarily conserved RNA-binding pocket ~16 Å away from the SAM pocket that also frequently mutates in cancer. We propose a two-step model of swiveling of target A upon conversion to m 6 A and sensing its methylation status by this pocket, enabling it to actuate enzymes' switch from writer to an m 6 A-sensor. Cancer-associated mutations show impaired RNA binding dynamics, de-stacking, and defective m 6 A writing and sensing.

Mechanical, physical and durability performance of engineered cementitious composites prepared with calcium aluminate cement

This research aims to fill a gap in existing studies by exploring the use of calcium aluminate cement (CAC) as an eco-friendly substitute for Ordinary Portland Cement (OPC) in Engineered Cementitious Composites (ECC). The study investigates the impact of CAC, both with and without the presence of fly ash (FA), on the mechanical, physical, durability, and microstructural properties of ECC-CAC mixtures. Various proportions of FA-to-CAC up to 1.5 were considered, while assessing different engineering parameters of compressive and flexural strengths, ductility, ultrasonic measurements, chloride penetrability, and drying shrinkage. Moreover, scanning electron microscopy (SEM) coupled with energy dispersive X-ray analysis (EDX) and X-Ray diffraction (XRD) were utilized to analyze the reaction products related to CAC and/or FA in selected mixtures. Higher strengths of CAC-ECC were achieved at earlier curing ages, though the transformation of CAC’s metastable phases led to reduced strengths in ECC-CAC mixtures compared to the control ECC during extended curing periods. Furthermore, the combination of FA with CAC played a crucial role in avoiding the hydrates conversion and minimizing the shrinkage in CAC-ECC, achieving even lower shrinkage levels than those observed in control OPC-ECC.

The effect of copper slag as a precursor on the mechanical properties, shrinkage and pore structure of alkali-activated slag-copper slag mortar

Copper slag, an industrial by-product produced in large quantities during copper smelting and refining, has the potential to be used as an alternative precursor for alkali-activated materials. This approach not only reduces the environmental impact of copper slag but also addresses the growing scarcity of conventional precursors, such as ground granulated blast furnace slag. In this research, copper slag was used as an alternative precursor for alkali-activated slag-copper slag mortars. Sodium hydroxide and water glass served as the activators. The workability, mechanical properties, autogenous shrinkage and drying shrinkage were investigated to evaluate the influence of copper slag content. Furthermore, the reaction products and pore structure of hardened mortar were analysed to gain deeper insights into its performance. The results show that the incorporation of copper slag effectively prolongs the setting time and increases the fluidity. Copper slag reduces the autogenous shrinkage, but it also results in an undesirable increase in drying shrinkage. While copper slag delays strength development and reduces the strength, incorporating copper slag at a 50 % ratio still results in strength comparable to that of mortars utilizing 100 % ground granulated blast furnace slag as the precursor. The incorporation of copper slag alters the composition of calcium aluminosilicate hydrate and promotes the formation of ferro-silicate. Although it reduces the proportion of macropores in the total pore volume, it simultaneously increases the amount of capillary pores. Copper slag alters pore solution, and although heavy metal leaching remains minimal, risks in complex environments require further study.

Effects of Frequency on the Performance of Ultrasonic Vibration Assisted Chemical Mechanical Polishing for Sapphire

Abstract Sapphire (Al2O3) is renowned for its exceptional properties, yet its unique natural presents a surface processing challenge. To enhance the polishing quality and efficiency, the sapphire ultrasonic vibration assisted chemical mechanical polishing (UV-CMP) has been proposed. This paper employs computational fluid dynamics (CFD) simulation and polishing experiments to investigate the action and mechanism of ultrasonic frequency on sapphire UV-CMP. The CFD simulation reveals that an increase in frequency can effectively elevate the fluid velocity, pressure, and cavitation. The enhancement in pressure, Z-direction, and resultant velocity has a positive impact on the cutting ability and utilization rate of nano-abrasives. A high frequency can enhance the physical fields of slurry, but it suppresses the growth of cavitation bubbles, and is detrimental to the number and size of abrasive particles. The best processing performance of sapphire UV-CMP is obtained at 40 kHz due to coordinated physicochemical interactions. X-ray photoelectron spectroscpy proves the product of solid-solid chemical reaction between nano-SiO2 and sapphire is softer Al2Si2O7 instead of Al2SiO5, which is beneficial to the material removal. This article provides theoretical and practical guidance for sapphire UV-CMP.

Capillary flow velocity-based length identification of PCR and RPA products on paper microfluidic chips.

This work demonstrates a novel, non-fluorescence approach to the length identification of polymerase chain reaction (PCR) and recombinase polymerase amplification (RPA) products, utilizing capillary flow velocities on paper microfluidic chips. It required only a blank paper chip, aminated microspheres, and a smartphone, with a rapid assay time and under ambient lighting. A smartphone evaluated the initial capillary flow velocities on the paper chips for the PCR and RPA products from various bacterial samples, where the pre-loaded aminated microspheres differentiated their flow velocities. Flow velocities were analyzed at different time frames and compared with the instantaneous flow velocities and interfacial tension (γLV) data. Subsequent error analysis justified the use of the initial time frames. A robust linear relationship could be established between the initial flow velocities against the square root of the product lengths, with R2 values of 0.981 for PCR and 0.993 for RPA. The assay seemed not to have a significant dependency on the cycle numbers and initial target concentrations. This novel method can be potentially used with various paper microfluidic methods of nucleic acid amplification tests towards rapid and handheld assays.

The fate of weakly bound light nuclei in central collider experiments: A challenge in favor of a late continuous decoupling mechanism

Arguments are presented that the reaction products of central high energy nuclear collisions up to collider energies can rigorously be interpreted in terms of a continuous decoupling mechanism based on continuous equations of motion. The various aspects of the collision dynamics are investigated in terms of the individual decoupling processes. Thereby each observed particle decouples during its own temporal decoupling window. This includes a “very late” decoupling of the faintly bound Hypertritons observed in recent ALICE experiments. The success of the strategy is based upon 200 years old wisdom and leads to a revised interpretation of the entire decoupling process.

Assessment of Nuclear Fusion Reaction Spontaneity via Engineering Thermodynamics.

This work recalls the basic thermodynamics of chemical processes for introducing the evaluation of the nuclear reactions' spontaneity. The application and definition of the thermodynamic state functions of the nuclear processes have been described by focusing on their contribution to the chemical potential. The variation of the nuclear binding potentials involved in a nuclear reaction affects the chemical potential through a modification of the internal energy and of the other state functions. These energy changes are related to the mass defect between reactants and products of the nuclear reaction and are of the order of magnitude of 1 MeV per particle, about six orders of magnitude larger than those of the chemical reactions. In particular, this work assesses the Gibbs free energy change of the fusion reactions by assuming the Qvalue as the nuclear contribution to the chemical potential and by calculating the entropy through the Sackur-Tetrode expression. Then, the role of the entropy in fusion processes was re-examined by demonstrating the previous spontaneity analyses, which assume a perfect gas of DT atoms in the initial state of the fusion reactions, are conservative and lead to assessing more negative ΔG than in the real case (ionized gas). As a final point, this paper examines the thermodynamic spontaneity of exothermic processes with a negative change of entropy and discusses the different thermodynamic spontaneity exhibited by the DT fusion processes when conducted in a controlled or uncontrolled way.

Ultrabright silicon nanoparticles combined with o-phenylenediamine for ratiometric fluorescence and smartphone imaging dual-mode detection of nitrite

Nitrite (NO2−) is widely present in the natural environment and human daily life. Excessive NO2− can cause harm to the environment and human health. Herein, silicon nanoparticles (SiNPs) with a fluorescence quantum yield of up to 70 % were synthesised using a one-pot hydrothermal method and combined with the common and inexpensive o-phenylenediamine (OPD) to achieve the detection of NO2−. Upon the addition of NO2−, the blue fluorescence of the SiNPs was quenched due to static quenching and Förster resonance energy transfer (FRET), while the yellow fluorescence of benzotriazole, the reaction product of OPD and NO2−, was enhanced, resulting in the fluorescence color change from blue to yellow. Based on these phenomena, a ratiometric fluorescence sensor integrated with smartphone imaging technology was developed. This sensor is notable for its portability, cost-effectiveness, and satisfactory detection limits (0.016 μM for ratiometric fluorescence and 1.64 μM for smartphone imaging). Importantly, it demonstrates high reliability and practicability in detecting NO2− in real water and food samples. This broadens the application of SiNPs in the sensing field and introduces new possibilities for NO2− detection in complex sample matrices.

Theoretical Investigation of the Reaction of O(1D) with Formamide.

Carbamic acid (H2NCOOH) is a small organic molecule that is terrestrially unstable in condensed phases under ambient conditions but could survive in the low densities and temperatures of the interstellar medium. In this work, the reaction of formamide (H2NCOH) and electronically excited oxygen atoms in the 1D state, namely, O(1D), has been investigated computationally to determine the feasibility of carbamic acid production. Geometries for carbamic acid and other potential reaction products have been calculated, as well as all pertinent transition states. In addition, harmonic and anharmonic frequency calculations were performed to determine quartic and sextic centrifugal distortion constants for all products. This work enables spectroscopic predictions that can guide the experimental search for carbamic acid. Presented here are the calculations, geometries, molecular constants, and spectral predictions for possible products of the reaction between formamide and O(1D), as well as a discussion of which products are favored.

Ethyl levulinate regulates traditional sulfolane biphasic absorbent for energy-efficient CO2 capture

Traditional CO2 biphasic absorbents currently suffer from problems such as high initial phase separation loading, poor product distribution selectivity, and weak dynamic phase separation ability, which limit their potential for industrial applications. This study developed a biphasic absorbent regulated by dual physical solvents by introducing partial ethyl levulinate (EL) into a sulfolane biphasic system. The optimal composition of this system was 30 wt% 1-amino-2-propanol (MIPA), 20 wt% sulfolane and 30 wt% EL. Under dual physical solvent conditions, strong electrostatic attraction between MIPA and CO2 promoted generation of MIPA zwitterions and carbamate. Analysis of the interactions between different product components through electrostatic potentials and with an independent gradient model based on Hirshfeld's partitioning revealed only extremely weak van der Waals force-driven interactions between the reaction products and EL. These interactions substantially reduced the initial phase separation loading and offered precise control over phase transition behavior. Compared with MIPA/sulfolane system, the MIPA/sulfolane/EL system achieved a 48.9 % lower initial phase separation loading, an 11.6 % lower proportion of saturated rich phase volume, a 10.1 % higher CO2-rich phase loading, and a 6.7 % lower viscosity. The excellent dynamic phase separation performance was verified using a customized device and the energy consumption for CO2 regeneration decreased to 2.2 GJ/t CO2.

Exploring Border Conditions for Spontaneous Emergence of Chirality in Allylboration of 1,2,3-Triazolic Aldehydes.

A case of spontaneous chirality generation was observed during a synthetic project studying the allylboration of 1,2,3-triazolic aldehydes. Here, we present computational studies supported by experimental findings targeting the elucidation of border conditions required for the observation of spontaneous chirality generation in the reaction of 1-Ar-1H-1,2,3-triazole-4-carbaldehydes 1a,b with triallylborane. Three possible sources of symmetry breaking were found computationally. Thus, dimerization of the initial reaction products, alcoholates 4a,b, gives dimers 5a,b (homochiral) and 6a,b (heterochiral). The latter were computed to be more stable thermodynamically, which can lead to amplification of the initial stochastic imbalance of the enantiomers of 4a,b via the reservoir mechanism. Furthermore, enantiomeric excess can be increased during the transfer of the second allylic group in the reaction of optically active boronates 4a,b with 1a,b, which was computed to be enantioselective due to the strong activating and stereoregulating properties of the 1,2,3-triazole group. In addition, reactions of borinic esters 8a,b, products of the previous reaction with triallylborane, recovered in each case two molecules of 4a,b of the same handedness, which can lead to additional chirality amplification. Experimentally, reactions of optically active alcohols (+)-R-2a,b with triallylborane provided chiral alcoholates 4a,b, which were reacted with equivalent amounts of corresponding aldehydes 1a,b. Unexpectedly, in two series of 10 experiments each, preferential formation of both enantiomers of the newly formed product was observed: seven times S and three times R in the case of 1a and six times S and four times R in the case of 1b.

Physical and chemical characteristics and activity of nickel-modified cobalt-iron-containing catalysts in the reaction of dry reforming of methane

In the process of dry reforming of methane (DRM), the activity of low-percentage catalysts based on cobalt and iron oxides and their modification with nickel oxide was studied. It has been established that the addition of nickel oxide into the Fe2O3/γ-Al2O3 catalyst increases the degree of methane conversion from 14 to 89%, and also increases the yield of target reaction products H2 to 43.0 vol.%, CO to 46.1 vol.% at 850 °C. On a Co3О4-NiО/γ-Al2O3 catalyst at 850 °C, methane conversion reaches to 88.1%, the yield of H2 and CO is 44.8%. TPR-H2 analyzes showed that the introduction of nickel oxide into Fe2O3/γ-Al2O3 composition, in contrast to the Co3O4/γ-Al2O3 catalyst, the temperature peaks of Fe2O3-NiО/γ-Al2O3, reduction shift towards lower temperatures and weaken the interaction of metals with the support - γ-Al2O3 and thereby the amount of active reduced particles of iron and nickel oxides increases, which ensures good catalytic activity of Fe2O3-NiО/γ-Al2O3. According to the XRD results, spinel-like form - NiFe2O4, NiAl2O4 and CoAl2O4, also phase as Fe2O3 were obtained on the Fe2O3-NiО/γ-Al2O3 catalyst. This indicates that the developed catalysts form new phases that are active at high temperatures to produce synthesis gas in reduction-oxidation processes during the DRM reaction.

Silicomanganese fume-based alkali-activated mortar: experimental, statistical, and environmental impact studies.

This paper evaluates the flowability and strength properties of alkali-activated mortar produced using silicomanganese fume (SiMnF) as the sole binder, combined with alkaline activators and sand, cured at room temperature (23 ± 1 °C). A total of 18 mixes were prepared by varying binder content (370, 470, and 570 kg/m3), alkaline activator content (33, 43, and 53% of binder by weight), and NaOH concentration (8 M and 12 M). The SiMnF-based alkali-activated pastes were characterized using SEM, XRD, and FTIR techniques to study morphology, mineral composition, and functional groups, respectively. Statistical modeling, including analysis of variance (ANOVA) and response surface method (RSM), was performed to optimize the mixes, and a life cycle assessment was conducted to evaluate the environmental impact of the developed SiMnF-based alkali-activated mortars (SiMnF-AAM). The experimental results showed that an optimal mix design with 470kg/m3 SiMnF, 43% alkaline activator content, and NaOH concentrations of 8M and 12M achieved the best balance of flow and strength. XRD and FTIR analyses confirmed that Nchwaningite was the primary reaction product, with secondary phases including magnetite, manganese ferrite, and potassium feldspar, influenced by alkali concentration. The SiMnF-based mixtures had a significantly lower CO₂ footprint (0.08kg CO₂/kg) compared to the cement-based mix, with alkali activators being the primary contributors to emissions. The developed SiMnF-AAM mixes, cured at room temperature, exhibited improved workability, mechanical properties, and reduced environmental impact, making them adaptive to real-life applications.

ENZYMES AND METABOLITES OF ENDOGENOUS CARBON MONOXIDE IN THE FETOPLACENTAL SYSTEM DURING PHYSIOLOGICAL GESTATION AND PLACENTAL DYSFUNCTION

Introduction. Prenatal ontogenesis largely depends on the functional and metabolic viability of the placenta and the entire fetoplacental complex. That is why the dysfunction of the placenta due to the changes in cellular regulation processes will lead to pregnancy complications and impaired fetal develop-ment. An important component of the system of intra- and intercellular regulators is the gas transmitter – carbon monoxide. Its role in cellular signaling and communication reactions, and at the same time, insufficient data of its metabolism, justifies the need to conduct research on this gas transmitter during complicated pregnancy. The aim of the work. To study the features of the metabolism of the active cellular mediator - the gas transmitter carbon monoxide in different objects of the fetoplacental system during physiological pregnancy and placental dysfunction. Material and methods. The research materials included placental tissue, amnion and amniotic fluid. The work uses spectrophotometric methods, enzyme immunoassay, and ion exchange chromatography. Results. Multidirectional changes in the activity of the studied enzymes (heme oxygenase and histidine decarboxylase), the content of the substrate of His-tidine reaction and the product of reaction of Histamine are established in case of placental disfunction. There is a certain correlation between the discov-ered studied components. Indicators of carbon monoxide metabolism can be markers for predicting postnatal damage – cerebral disorders in newborns. Conclusions. The identified injuries are obviously important links in the chain of disorders accompanied by the development of placental dysfunction.

Toxoplasma Gondii In Association with TLR4 Among Regular Hemodialysis Patients

Background: Hemodialysis patients can be considered immunocompromised as they have an increased risk of infections. The activity of Toll -like receptors in defense against infections was observed particularly for Toll like receptor4 molecule. Several single-nucleotide polymorphisms (SNPs) residing in genes encoding Toll -like receptors were reported as significant genetic modifications associated with infections. Aim: To determine the association between Toll- like receptors 4 polymorphisms and the susceptibility to infection with Toxoplasma gondii in hemodialysis patients. Materials and Methods: This case- control study was conducted on 150 patients with hemodialysis and 150 apparently healthy blood donors as control group, the samples were collected in the period from march 2021 to November 2021 from Al-Karama hospital and Al-Yarmouk Teaching Hospital. All patients were investigated for the presence of Toxoplasma gondii and Abs (IgG, IgM) by using ELISA technique and conformation by molecular technique (Real time-PCR). The selected SNPs in Toll- like receptors 4 were amplified by using conventional polymerase chain reaction PCR and then sequencing there polymorphism. Results: In the current study the comparison of median age between patients and controls was with no significant difference, while the laboratory tests revealed significant difference in median level of urea, creatinin , calcium , potassium ,albumin and hemoglobin, and insignificant difference for body mass index and sodium between studied groups. The ratio of females infected with Toxoplasma gondii was higher than infected males. The seropositive result in patients for Toxoplasma gondii - IgG and IgM was 15 and 6 respectively while 19 patients were positive by PCR. However in control group there were 8 patients seropositive for IgG and positive in PCR results while the results of IgM and PCR were negative for all control group. The Polymerase chain reaction (PCR) products of Toll- like receptors 4 genes were subjected for direct sequencing by using Bio edit software. And the resultant sequences were compared with reference sequences in NCBI. The analysis of TLR-4 rs4986790 genotypes were 24(80%) AA and 6(20%) AG in patients while 6 (60%) AA and 4(40%) AG in controls with insignificant difference, while the analysis of TLR-4 rs4986791 genotypes were 24(80%) CC and 6 (20%) CT in patients while 6 (60%) CC and 4(40%) CT in controls with insignificant difference. Conclusion: There was no significant association of Toxoplasma gondii with TLR4 genotypes of rs4986790 and rs4986791 SNPs in hemodialysis patients.

Antibacterial activity and preservative effect for pork tenderloin of chitosan -glucosamine Maillard reaction products prepared by gamma irradiation

Antibacterial activity and preservative effect for pork tenderloin of chitosan -glucosamine Maillard reaction products prepared by gamma irradiation