pH Values Research Articles

Impact of pH-mediated in situ enzymatic pretreatment on food waste decomposition and biomethane production: Performance, mechanism, and key metabolic pathways

pH value universally presents the great influence on hydrolysis efficiency of food waste (FW) by in situ enzymatic pretreatment, while the influencing mechanism of pH value on enzymatic decomposition of FW is not clear at present. This study innovatively in situ prepared a microbial-based compound enzyme (MCE) from FW, as well as systematically deciphered the impact and underlying mechanism of pH-mediated MCE pretreatment on FW decomposition and biomethane production. The dissolution, biodegradability and monomer formation of FW were found to be promoted by MCE pretreatment, and the highest hydrolysis efficiency was obtained at pH 5, while the biomethane yield was accordingly increased by 30.89 % compared to the control. The dissection of Fourier transform infrared spectroscopy (FTIR) results unraveled that the reaction order of FW components was protein → lipid → starch → cellulose in the acid-enhanced process, while the order shifted to starch → protein → cellulose → lipid in the alkali-enhanced process. Moreover, the looser protein structure was obtained after MCE pretreatment due to α-helix/(β-sheet + random coil) value was declined from 60.35 % to 57.01 %-49.03 %. These changes induced by pH-mediated MCE pretreatment reshaped the bacterial microbial community in favor of biomethane production, and the metagenomic analysis further demonstrated that MCE pretreatment had the highest abundances of genes related to metabolic functions of level 2 and 3 at pH 5, while the abundances of over 90 % key enzyme-encoding genes associated with hydrolysis, acidogenesis and methanogenesis were also increased during the anaerobic digestion process, therefore harvesting the highest biomethane yield.

Sensitively detection of ascorbic acid in orange samples with ionic liquid functionalized carbon dots and lanthanide complexes

In the food industry, ascorbic acid (AA) is widely used as an antioxidant. However, the concentration of AA is influenced by various factors, including temperature, time, and pH value during food preparation and storage, leading to its instability in content. This makes the accurate detection of AA content particularly important. Precise determination of AA content in food and pharmaceuticals is crucial for ensuring the adequate intake of essential vitamins and maintaining good health. Herein, we have developed a successful preparation method of an imidazole-based ionic liquid functionalized CDs hybrids APM-CDs. A novel photo functional hybrid probe Eu3+@APM-CDs was obtained via an ion-exchange reaction between APM-CDs and lanthanide complex Eu(DPA)3. The obtained hybrid probe was extensively characterized in detail. What's more, the results show that the fluorescent intensity of Eu3+@APM-CDs has a good linear response to AA concentrations in the range of 25–500 μM (R2 = 0.99), with a detection limit of 80 nM. The fluorescence probe demonstrates good selectivity and sensitivity toward AA and has the potential for significant application in AA detection by simplifying procedures and reducing interference from impurities.

Fabrication of Rhenium Disulfide/Mesoporous Silica Core-Shell Nanoparticles for a pH-Responsive Drug Release and Combined Chemo-Photothermal Therapy.

A stimuli-responsive drug delivery nanocarrier with a core-shell structure combining photothermal therapy and chemotherapy for killing cancer cells was constructed in this study. The multifunctional nanocarrier ReS2@mSiO2-RhB entails an ReS2 hierarchical nanosphere coated with a fluorescent mesoporous silica shell. The three-dimensional hierarchical ReS2 nanostructure is capable of effectively absorbing near-infrared (NIR) light and converting it into heat. These ReS2 nanospheres were generated by a hydrothermal synthesis process leading to the self-assembly of few-layered ReS2 nanosheets. The mesoporous silica shell was further coated on the surface of the ReS2 nanospheres through a surfactant-templating sol-gel approach to provide accessible mesopores for drug uploading. A fluorescent dye (Rhodamine B) was covalently attached to silica precursors and incorporated during synthesis in the mesoporous silica walls toward conferring imaging capability to the nanocarrier. Doxorubicin (DOX), a known cancer drug, was used in a proof-of-concept study to assess the material's ability to function as a drug delivery carrier. While the silica pores are not capped, the drug molecule loading and release take advantage of the pH-governed electrostatic interactions between the drug and silica wall. The ReS2@mSiO2-RhB enabled a drug loading content as high as 19.83 mg/g doxorubicin. The ReS2@mSiO2-RhB-DOX nanocarrier's cumulative drug release rate at pH values that simulate physiological conditions showed significant pH responsiveness, reaching 59.8% at pH 6.8 and 98.5% and pH 5.5. The in vitro testing using HeLa cervical cancer cells proved that ReS2@mSiO2-RhB-DOX has a strong cancer eradication ability upon irradiation with an NIR laser owing to the combined drug delivery and photothermal effect. The results highlight the potential of ReS2@mSiO2-RhB nanoparticles for combined cancer therapy in the future.

Unspecific Peroxygenase (UPO) can be Tuned for Oxygenation or Halogenation Activity by Controlling the Reaction pH.

Unspecific Peroxygenases (UPOs) are increasingly significant enzymes for selective oxygenations as they are stable, highly active and catalyze their reactions at the expense of only hydrogen peroxide as the oxidant. Their structural similarity to chloroperoxidase (CPO) means that UPOs can also catalyze halogenation reactions based upon the generation of hypohalous acids from halide and H2O2. Here we show that the halogenation and oxygenation modes of a UPO can be stimulated at different pH values. Using simple aromatic compounds such as thymol, we show that, at a pH of 3.0 and 6.0, either brominated or oxygenated products respectively are produced. Preparative 100 mg scale transformations of substrates were performed with 60-72% isolated yields of brominated products obtained. A one-pot bromination-oxygenation cascade reaction on 4-ethylanisole, in which the pH was adjusted from 3.0 to 6.0 at the halfway stage, yielded sequentially brominated and oxygenated products 1-(3-bromo-4-methoxyphenyl)ethyl alcohol and 3-bromo-4-methoxy acetophenone with 82% combined conversion. These results identify UPOs as an unusual example of a biocatalyst that is tunable for entirely different chemical reactions, dependent upon the reaction conditions.

Physicochemical, colour, microbiology, sensory and mineral attributes of set-type yoghurt produced from Gundelia tournefortii L. and its gum

AbstractThe present study aimed to investigate the production of yoghurt in which the parts of the Gundelia tournefortii L. and its gum were added to milk at levels of 3% (v/v), incubated until the pH value reached 4.7 at 42 °C and then stored at 4 °C for 21 days. The Ca, P, K, Na and Mg contents of the yoghurt sample containing Gundelia tournefortii L. proved to be higher than those found in the control sample. Acidity, acetaldehyde, viscosity, a* values of yoghurt samples increased during storage, while the volatile fatty acids, gel firmness, whey separation, water holding capacity, L* and the b* values were decreased. The lactic acid bacteria count on the 21st day was > 6 log CFU/g in all yoghurt samples. The total aerobic mesophilic bacteria decreased except for the yoghurt sample containing Gundelia tournefortii L. milk, while the yeast and mold increased. The preference map revealed that 60–80% of consumers were satisfied with the control sample and the Gundelia tournefortii L. gum sample. Gundelia tournefortii L. milk and Gundelia tournefortii L. leaves samples were also found to have acceptable scores. As a result, adding Gundelia tournefortii L. into the yoghurt turned out to have a positive impact on its sensory and functional properties and could lead to an innovative approach in the dairy product market. Graphical abstract

Sea surface acidification events in the Andaman Sea associated with the last Toba volcanic activity

To date, little is known about the impact of super-eruptions on ocean biogeochemistry. Using boron isotopes ratios measured on planktonic foraminifera in the marine sediment core BAR94–25, we provide a high-resolution pH record in the Andaman Sea (North of Sumatra), spanning Marine Isotopic Stage 5 to 3. This transition encompasses the super-eruption of the Toba volcano, 74,000 years ago, making it possible to decipher the potential impact of the super-eruption emissions on the ocean pH for the first time. Our results show that inferred foraminiferal pH values generally follow those predicted by glacial-interglacial CO2 variations. However, several abrupt pH drops coincide with Toba ash deposition. This suggests the occurrence of acidification events possibly related to Toba volcanic sulphur emission episodes. These pH drops are followed by anomalous pH increases, possibly relating to localised increases in seawater alkalinity following the alteration of large ash deposits on land.

A highly stable membrane-free potentiometric pH sensor with nickel cobalt sulfide as the solid contact layer and ion recognition

In this work, a new NiCo2S4 based H+ ion-selective electrode (ISE) without a polymer membrane was proposed and used to rapidly monitor the pH values of wetland soils in the Yellow River Delta in China. This NiCo2S4-based potentiometric pH sensor without an ion-selective membrane (ISM) exhibited a near-Nernstian response slope (50.9 ± 0.4 mV/dec) and good sensitivity. Furthermore, the developed pH sensors using NiCo2S4 as a solid contact (SC) layer present good reproducibility and the standard deviation of Eo is only 0.75 mV (n = 6). The water layer at the SC/ISM interface of the NiCo2S4-based membrane-free potentiometric pH sensor vanished, thus yielding excellent long-term potential stability (8.6 ± 0.4 μV/h over 264 h). This pH sensor offers a new design strategy for the construction of miniaturized highly stable ISEs without ISM.

Effect of temperature and spawning agents on wild female asp (Leuciscus aspius) reproductive efficiency under controlled conditions

Artificial reproduction is a bottleneck to produce stocking material for many species of freshwater fish. One of these species is the asp, Leuciscus aspius. Research in the field of artificial reproduction of this species is very scarce and often incomplete. There are no breeding protocols specifying optimal environmental conditions and hormonal stimulation for many species of rheophilic cyprinids, including asp. Since the number of natural asp populations is constantly decreasing, it is important to support natural stocks by restocking with high quality stocking material. For this reason, optimized protocols are needed to breed this species under controlled conditions to produce stocking material with high biodiversity and good health. Such an approach will make it possible to maintain the population of natural asp at a constant level. The aim of this study was to develop the protocol of asp artificial reproduction using optimized thermal conditions and appropriate hormonal stimulation. In experiment I, the influence of constant temperature (10.0, 12.0 and 14.0 °C) on the effectiveness of artificial reproduction of asp. In experiment II, the effectiveness of asp reproduction was checked after the application of spawning agents: Ovopel, Ovaprim or a combination of these two agents The obtained results indicate that for the final maturation of oocytes (FOM) and artificial reproduction of asp in controlled conditions, water temperatures of 10–12 °C are the most useful. Under these thermal conditions, the highest percentages of female’s ovulation and embryo survival, as well as the percentage of hatching, were obtained. Hormone injections are necessary to perform final oocyte maturation (FOM) in female asp in captivity. All spawning agents used were especially useful for artificial reproduction of asp, however, the best values of the studied indices, such as ovulation rate and embryo survival, were obtained after the application of Ovaprim or the combination of Ovopel and Ovaprim in water temperature at a range of 10–12 °C. It was found that the pH of ovarian fluid may be a preliminary indicator of the biological quality of eggs in asps. The optimal pH value is 8.0–8.4. At pH below 7.4, no viable embryos were observed.

A novel approach for the lifetime prediction and structural health monitoring of concrete sewer systems exposed to biogenic sulphide corrosion

A novel, combined experimental-modelling approach is presented for the estimation of the corrosion depth, load bearing capacity and lifetime of unreinforced concrete sewer pipes exposed to prolonged biogenic sulphide corrosion. The biogenic sulphide corrosion process is mimicked through two types of representative chemical experiments, namely: (i) long-term experiments performed under moderately controlled pH conditions, where dry-cast concrete cube samples are exposed to monthly refreshed sulphuric acid solutions with initial pH values of 3, 2 and 1 for a period of 12 months, and (ii) short-term experiments carried out under highly controlled pH conditions, in which dry-cast concrete disk samples are subjected to sulphuric acid solutions with almost constant pH values of 2, 1 and 0.5 for a period of two months. By applying X-ray diffraction, optical microscopy, scanning electron microscopy and energy dispersive X-ray spectroscopy analyses, insight into the micro-scale morphology and elemental composition of the corrosion profile is obtained. In addition, the corrosion front and depth characteristics are measured by conducting phenolphthalein tests and analyses of surface colour and texture of macro-scale samples. From the experimental results, the time course of the corrosion depth is calibrated with a model for sulphate attack under a constant pH level. The model formulation is combined with detailed finite element method results from the literature to predict the long-term load bearing capacity of a concrete sewer pipe. The model is subsequently generalised for sulphate corrosion under a varying pH level. When combined with the installation of pH measuring devices on the inside of sewer pipes, the current engineering model may serve as an excellent practical tool for continuously monitoring the structural health and predicting the lifetime of in-situ sewer systems subject to sulphate attack under random acidity fluctuations.

Reactive liquid-liquid extraction of lactic acid from microfiltered sweet sorghum silage press juice in an agitated extraction column using a hydrophobic natural deep eutectic solvent as modifier

Downstream processing of carboxylic acids from fermentation broths is cost-intensive and environmentally harmful, which makes methods such as reactive liquid-liquid extraction attractive separation technologies. To enhance the sustainability of liquid-liquid extraction processes, research focuses on sustainable solvents like hydrophobic natural deep eutectic solvents. However, the application of hydrophobic natural deep eutectic solvents in agitated extraction columns for continuous processing has never been investigated. This is essential to facilitate their use in industrial processes, promoting cleaner production. In this study, the application of a thymol-menthol-based deep eutectic solvent as a modifier (with the extractant tri-n-octylamine) in an agitated extraction column is evaluated for reactive liquid-liquid extraction of lactic acid from microfiltered sweet sorghum silage press juice. In addition, three-stage cross-current extractions were performed. The thymol-menthol-based deep eutectic solvent showed efficient phase separation, stable operation, and chemical stability in the agitated extraction column. In three-step cross-current operation, the extraction efficiency for lactic acid was increased from 37.0 ± 0.4 % without feed pH adjustment to 76.2 ± 0.9 % with continuously adjusting the pH value to 2.05 ± 0.02. The thymol-menthol-based deep eutectic solvent shows great potential for application in agitated extraction columns. This is highly promising because natural deep eutectic solvents can enhance the sustainability of extraction processes and reduce the reliance on fossil-based solvents.

Adsorption of Cu (II) and Zn (II) in aqueous solution by modified bamboo charcoal.

Due to the development of industries such as mining, smelting, industrial electroplating, tanning, and mechanical manufacturing, heavy metals were discharged into water bodies seriously affecting water quality. Bamboo charcoal, as an environmentally friendly new adsorbent material, in this paper, the virgin bamboo charcoal (denoted as WBC) was modified with different concentrations of KMnO4 and NaOH to obtain KMnO4-modified bamboo charcoal (KBC) and NaOH-modified bamboo charcoal (NBC) which was used to disposed of water bodies containing Cu2+ and Zn2+. The main conclusions were as following: The adsorption of Cu2+ by WBC, KBC and NBC was significantly affected by pH value, and the optimum pH was 5.0. Differently, the acidity and alkalinity of the solution doesn't effect the adsorption of Zn2+ seriousely. Meanwhile, surface diffusion and pore diffusion jointly determine the adsorption rate of Cu2+ and Zn2+. The test result of EDS showed that Mn-O groups formed on the surface of K6 (WBC treated by 0.06mol/L KMnO4) can promote the adsorption of Cu2+ and Zn2+ at a great degree. The O content on N6(WBC treated by 6mol/L NaOH) surface increased by 30.95% compared with WBC. It is speculated that the increase of carbonyl group on the surface of NBC is one of the reasons for the improvement of Cu2+ and Zn2+ adsorption capacity. Finally, the residual concentrations of Cu2+ and Zn2+ in wastewater are much lower than 0.5mg/L and 1.0mg/L, respectively. Thus it can be seen, KBC and NBC could be a promising adsorbent for heavy metals.

PH‐responsivity and photoconductivity for the organic mixed ionic electronic conductor of PANI/PSS composite films

AbstractThe influence of ionic‐electronic coupling on the electrical conductivity and the photoconductivity of organic mixed ionic electronic conductor (OMIECs) of polyaniline/poly (4‐styrene sulfonic acid) (PANI/PSS) composite films. PANI/PSS composite films are connected by blending the carbon atoms within the aromatic ring in PANI with sulfonate groups in PSS. The electrical conductivity of PANI/PSS composite film increases from to as the pH value increases from 3 to 9. The electrical conductivity of PANI/PSS composite films for all pH values increases continuously as the temperature increases. Additionally, the PANI/PSS composite films exhibit photo responses at UV light since the band structure can absorb the light in this region. The photoconductivity curves of PANI/PSS composite films for different pH values exhibit good consistency and repeatability. Modeling raising photoconductivity and decaying conductivity after light off leads us to understand the underlying physics of the ionic‐electronic coupling and other parameters on the photoconductivity of OMIECs, consequently building OMIEC devices for different photoconductivity applications.

Engineering of chimeric enzymes with expanded tolerance to ionic strength.

Antimicrobial resistance poses a significant global threat, reaching dangerously high levels as reported by the World Health Organization. The emergence and rapid spread of new resistance mechanisms, coupled with the absence of effective treatments in recent decades, have led to thousands of deaths annually from infections caused by drug-resistant microorganisms. Consequently, there is an urgent need for the development of new compounds capable of combating antibiotic-resistant bacteria. A promising class of molecules exhibiting potent bactericidal effects is peptidoglycan hydrolases. Previously, we cloned and characterized the biochemical properties of the M23 catalytic domain of the EnpA (EnpACD) protein from Enterococcus faecalis. Unlike other enzymes within the M23 family, EnpACD demonstrates broad specificity. However, its activity is constrained under low ionic strength conditions. In this study, we present the engineering of three chimeric enzymes comprising EnpACD fused with three distinct SH3b cell wall-binding domains. These chimeras exhibit enhanced tolerance to environmental conditions and sustained activity in bovine and human serum. Furthermore, our findings demonstrate that the addition of SH3b domains influences the activity of the chimeric enzymes, thereby expanding their potential applications in combating antimicrobial resistance.IMPORTANCEThese studies demonstrate that the addition of the SH3b-binding domain to the EnpACD results in generation of chimeras with a broader tolerance to ionic strength and pH values, enabling them to remain active over a wider range of conditions. Such approach offers a relatively straightforward method for obtaining antibacterial enzymes with tailored properties and emphasizes the potential for proteins' engineering with enhanced functionality, contributing to the ongoing efforts to address antimicrobial resistance effectively.

The enhancement of photocatalytic hydrogen production over Ag2WO4 modified g-C3N4 with Pt as cocatalyst

ABSTRACT The construction of heterojunction photocatalyst is an effective mean to improve the photoexcited electron–hole pair separation. The Ag2WO4-doped graphitic carbon nitride (g-C3N4, C3N4 for short) composite photocatalysts were fabricated by a simple calcination and in-situ depositing strategy. The composites were characterized by different techniques. The effects of Ag2WO4 content, type of scavengers, pH value of reaction solution and dose of scavenger on photocatalytic hydrogen (H2) generation were studied. It was found that the Ag2WO4 micro-nano particles were highly dispersed on the C3N4 surface. After doping Ag2WO4, the light absorption range of Ag2WO4-C3N4 material was broadened effectively from 440 nm to 448 nm, and the BET surface area of C3N4 was increased from 35.63 to 40.73 cm2·g−1, indicating that Ag2WO4 loading could provide some new BET surface areas. The binding energy of all elements in Ag2WO4-4/C3N4 was clearly shifted due to the charge transfer from C3N4 to Ag2WO4, implying a strong interaction between C3N4 and Ag2WO4. The photocatalytic H2 production rate of the optimized Ag2WO4-4/C3N4 was 6047.4 μmol·g−1·h−1, which was 2.04 and 171.8 times that of C3N4 and Ag2WO4, respectively. While Ag2WO4-4/C3N4 exhibited a poor H2 production performance in the absence of Pt co-catalyst (309.3 μmol·g−1·h−1), indicating the formation of heterojunction among Ag2WO4, C3N4 and Pt.

Real-time and high-sensitive colorimetric sensor based on photonic crystal for amniotic fluid identification

In this study, we proposed a pH-responsive photonic crystal hydrogel sensor (PCHs) to conveniently and accurately recognize the amniotic fluid from urine of parturient women, which was constituted by three-dimensional polymethyl acrylamide (PMMA) array and optimized hydrogel. PMMA array was self-assembled by 180 nm monodispersed nanoparticles with vertical sedimentation method. The functional hydrogel containing N-acryloyl phenylalanine (APA), acrylamide (AM) and N, N'-methylene bis(acrylamide) (BIS) as co-monomer and crosslinking agent respectively, was photo-polymerized by the precursor under 365 nm UV light. This hydrogel significantly shrank or swelled corresponding to the acidity and alkalinity of the aqueous solution, which resulted in both the reflection peak position (λmax) of the prepared sensor and its structural color changing with the pH value. The λmax of PCHs redshifted from 514 nm to 606 nm in 60 s while the pH value of testing solution increased from 4.5 to 8.0, which exactly covered the pH value of amniotic fluid and urine. Correspondingly, its structure color gradually changed from pale-green to red ensuring their naked-eye determination. Furthermore, an extremely high sensitivity as 26.3 nm/pH of Δλmax was obtained which was linearly related to pH value. The prepared sensor possessed steady accuracy and extraordinary sensitivity compared with the pH test strip which was generally used in amniorrhexis diagnosis nowadays besides the advantages of the low cost, simple operation, rapid response and visual detection mode. The reliability of this PCHs was further confirmed by the real sample detection which relative standard deviation was below 5.0 %, suggesting its potential clinical applications.

Interfacial and foaming properties of soluble lupin protein isolates: Effect of pH

Lupins are rich in proteins (∼40%) and fibers (∼40%), and have been widely used for animal feed, but limitedly for human consumption due to the presence of alkaloids. Due to their high protein content, lupins have a high potential to be used as protein sources in diverse food manufacturing processes, including emulsion and foam stabilization. However, the interfacial properties of lupin protein isolates (LPI), especially their performance at different pH values, are not well understood so far. Here, we systematically investigated the air-water interfacial and foaming properties of the soluble fraction of LPI at pH 7.0, pH 6.0, pH 4.0, and pH 3.5. We observed that LPI at pH 4.0 (LPI-4) and pH 3.5 (LPI-3.5) adsorbed faster at the air-water interface than at pH 7.0 (LPI-7) and pH 6.0 (LPI-6) due to a smaller particle size and higher surface hydrophobicity of LPI-4 and LPI-3.5. This resulted in a higher foam overrun of LPI-4 and LPI-3.5 (300% and 331%, respectively). The air-water interfaces formed by LPI at different pH values were dramatically different in terms of interfacial structure and mechanical properties. LPI-4 and LPI-3.5 formed stiff and solid-like interfaces, leading to higher foam stability. In contrast, for LPI-7 there were clearly more protein aggregates at the interface, and this structure was weaker and less stretchable in response to shear and dilatational deformation, causing lower foam stability. LPI-6 also showed weaker air-water interfaces and thus formed less stable foams. Overall, LPI at acid pH (3.5 and 4) has a better performance in foam stabilization than at a pH close to neutral (6 and 7). Our results suggest that LPI can be potentially used as a plant-based clean-label additive in the production of foam-based food products in acidic environments.

Preparation and Study of the Effect of pH Value on Structural, Morphological, Electrical and Magnetic Properties of CoFe2O4 Nanoparticles Prepared by Sol-Gel Precipitation Method

The present study reports the synthesis of cobalt ferrite nanoparticles (CoFe2O4 NPs) using the sol-gel precipitation process via mixing a stoichiometric ratio of cobalt chloride (1 M) and ferric chloride (2 M).. The molar of ferric to cobalt was mentioned (2:1) and then 2 M of sodium hydroxide was added. The structural and morphological features of the material were assessed using X-ray diffraction (XRD), Scanning electron microscopy (SEM), and atomic force microscopy (AFM). The electrical properties were analyzed using an LCR meter, while the magnetic properties were measured using a vibrating sample magnetometer (VSM). Fourier-transform infrared spectroscopy (FTIR) investigated the material's molecular vibrations. The X-ray diffraction (XRD) analysis revealed that all the samples exhibited a cubic spinal structure, and no additional peak was detected. Interestingly, the average size of the crystallites (D) decreased from 17.74 nm to 16.58 nm as the pH level increased from 7 to 13. This finding provides important insights into the behaviour of the tested samples under different pH conditions. The formation of the ferrite spine was confirmed by FTIR spectroscopy, with the primary detected bands (408.92 - 470.65 cm-1) attributed to the octahedral complexes and (516.94 - 588.31 cm-1) assigned to the tetrahedral ones. The dielectric and imaginary part of the dielectric constant decreased with increasing pH values excluding samples prepared at pH = 11. All samples with different pH values exhibit resonance peaks at frequencies up to (1 KHz). The magnetic measurements carried out by the VSM instrument, the result show that the saturation magnetization increases with increasing pH and the higher saturation magnetization is 68 emu. g1.

Decolorization of C.I. Reactive Blue 78 dyeing wastewater in the chitosan-gelatin composite copper polymer/sodium persulfate system

Chitosan-gelatin composite copper polymer (CG for short) was prepared as an adsorption catalyst. The CG was combined with sodium persulfate to construct a heterogeneous Fenton-like system, which was applied to the decolorization of C.I. Reactive Blue 78 dyeing wastewater. The effects of sodium persulfate, CG, temperature, initial dyeing wastewater pH value and additives ( sodium chloride, sodium carbonate) on the decolorization were investigated. The results show that the decolorization percentage of 0.1g/L C.I. Reactive Blue 78 dyeing wastewater can reach 93.84% under the conditions of sodium persulfate dosage of 0.3g/L, CG dosage of 0.8g/L, decolorization at 40 °C for 30min. At the same time, the catalytic system has the characteristic of good decolorization effect on C.I. Reactive Blue 78 dyeing wastewater within a wide pH values range of 3~9. Even for dyeing wastewater containing 0.4g/L high concentration C.I. Reactive Blue 78, the decolorization percentage can reach over 90% after decolorization at 40 °C for hours. Moreover, CG can be reused. After repeated use of CG four times, the decolorization percentage of C.I. Reactive Blue 78 dyeing waste remains above 90%. In addition, the weight loss rate of CG after each decolorization is less than 12%. However, the presence of sodium chloride and sodium carbonate in the dyeing wastewater is not conducive to the decolorization of C.I. Reactive Blue 78 by the system.

Effect of grain size on the dielectric and magnetic properties of YFeO3 ceramics densified by microwave sintering and spark plasma sintering from powders synthesized via reverse chemical co-precipitation

YFeO3 (YFO) ceramics were synthesized by reverse co-precipitation at different pH values followed by microwave sintering (MS) and spark plasma sintering (SPS) techniques. Also, the effect of the grain size on the magnetic and dielectric properties of the sintered ceramics was examined using various characterization methods. Moreover, FESEM micrographs showed that the particle size of the calcined samples has declined by increasing the pH value. Furthermore, the magnetization curves exhibited weak ferromagnetic behavior in the pre-sintered powder samples. Besides, the Ms value was enhanced from 1.26emu/g to 2.3emu/g by an increase in pH from 8.5 to 10.5 owing to reducing the particle size and subsequently raising the amount of uncompensated surface spins. Furthermore, the powder samples showed an increase in the Hc and Mr values from 15Oe to 28Oe and 0.127emu/g to 0.296emu/g, respectively, with a reduction in particle size from 0.632μm to 0.272μm. Additionally, the specimens processed through the sintering techniques demonstrated a remarkable reduction in magnetic characteristics. Therefore, a decrease in magnetic saturation values from 2.3emu/g to 0.43emu/g for the MS sample and to 0.17emu/g for the SPS specimen was attributed to a marked reduction in the amount of free surfaces and subsequently uncompensated surface spins. At last, the observed dielectric characteristics of all the sintered pellets had a common dielectric behavior. This signifies that by increasing the frequency the and tanδ decline at lower frequencies and become frequency-independent at higher frequencies based upon the Maxwell-Wagner polarization theory. On the other hand, the value for the SPS sample produced at pH=10.5 underwent a decline of 2.5 times at the low frequency of 200Hz compared to the MS one due to the significant decrement of the grain boundaries on account of the coarsening of grains.

Fabrication and characterization of oxidized starch-xanthan gum composite nanoparticles with efficient emulsifying properties

This study involved the preparation of nanoparticles by combining oxidized starch (OS) with xanthan gum (XG), and emulsions were prepared from this nanoparticle. The physical and chemical characteristics, as well as the emulsification properties of oxidized starch-xanthan gum composite nanoparticles (OGNP), were analyzed. The findings revealed that the OGNP retained spherical shape after the addition of XG, although their diameter increased from approximately 50–150 to 200–400 nm. Zeta potential decreased with XG content. Moreover, emulsions prepared from OGNP exhibited outstanding thermal stability, also showing enhanced storage stability. In addition, emulsions had different rheological properties at different pH values. The apparent viscosity and shear stress of emulsions under alkaline conditions were lower than that of neutral conditions. NaCl increased the apparent viscosity of OGNP-stabilized emulsions while reducing their thermal stability. The nanoparticles prepared in this study have efficient emulsification properties and can extend the application of OS.