Improvement Of Acid Resistance Research Articles

Effect of the initial pH of the culture medium on the nutrient consumption pattern of Bifidobacterium animalis subsp. lactis Bb12 and the improvement of acid resistance by purine and pyrimidine compounds.

During fermentation, the accumulation of acidic products can induce media acidification, which restrains the growth of Bifidobacterium animalis subsp. lactis Bb12 (Bb12). This study investigated the nutrient consumption patterns of Bb12 under acid stress and effects of specific nutrients on the acid resistance of Bb12. Bb12 was cultured in chemically defined medium (CDM) at different initial pH values. Nutrient consumption patterns were analyzed in CDM at pH 5.3, 5.7, and 6.7. The patterns varied with pH: Asp+Asn had the highest consumption rate at pH 5.3 and 5.7, while Ala was predominant at pH 6.7. Regardless of the pH levels (5.3, 5.7, or 6.7), ascorbic acid, adenine, and Fe2+ were vitamins, nucleobases, and metal ions with the highest consumption rates, respectively. Nutrients whose consumption rates exceeded 50% were added individually in CDM at pH 5.3, 5.7, and 6.7. It was demonstrated that only some of them could promote the growth of Bb12. Mixed nutrients that could promote the growth of Bb12 were added to three different CDM. In CDM at pH 5.3, 5.7, and 6.7, it was found that the viable cell count of Bb12 was the highest after adding mixed nutrients, which were 8.87, 9.02, and 9.10 log CFU ml-1, respectively. The findings suggest that the initial pH of the culture medium affects the nutrient consumption patterns of Bb12. Specific nutrients can enhance the growth of Bb12 under acidic conditions and increase its acid resistance.

Ti3C2Tx MXene-derived hydroxyl-rich titanate based hybrid membrane with cellulose as structural regulator for highly-efficient disposition of heavy metal ions

Exploring an efficient and stable adsorbent material for purification of toxic heavy metal ions wastewater is of great significance. However, as a typical heavy metal ions adsorbent, titanate can still improve in material synthesis, adsorption efficiency and the recyclability. Herein, a novel titanate-based adsorbent which composing of Ti3C2Tx MXene-derived hydroxy-rich titanate and cellulose was fabricated for efficient removal of toxic heavy metal ions. Owing to the similar stratified structure, the conversion from Ti3C2Tx MXene to titanate is energy-saving and easy to achieve. In addition, the inherited hydroxy-rich property is beneficial to improve the adsorption efficiency of the derived titanate. Furthermore, the introduction of cellulose as a structural regulator to fabricate the titanate/cellulose membrane could greatly alleviate the problem of difficult recycling of powder adsorbent. Thus, the constructed Ti3C2Tx-derived hydroxy-rich titanate/cellulose membrane adsorbent (M-NTO/CM) exhibits high Cu2+ adsorption capacity of 2.63 mmol g−1 and can reach the adsorption equilibrium in only 5 min. Better yet, there has also been a significant improvement in acid resistance and recyclability of the M-NTO/CM relative to traditional titanate. In short, M-NTO/CM derived from Ti3C2Tx MXene can be used as an advanced membrane for convenient and efficient purification of heavy metal ions from the wastewater.

Corrosion behaviours of a LaB6/TiC/TiB/ti composite in neutral or acidic electrolytes

LaB6/TiC/TiB was incorporated into a Ti–Al–Zr–Sn alloy to achieve an efficient improvement in acid-resistance. The incorporation of LaB6/TiC/TiB deteriorated the performance of the passive layer, but impeded the penetration of the corrosive medium into Ti matrix. The incorporation of the conductive reinforcements promoted galvanic corrosion, leading to a decrease in barrier effect of the passive film. Delayed passivation in less aggressive media was achieved by controlling the formation and growth of corrosion pits. The distribution of LaB6/TiC/TiB determined the corrosion properties after complete failure of the passive layer. An appropriate approach for enhancing the acid-resistance of Ti-based materials was suggested.

Improvement in Acid Resistance of Polyimide Membranes: A Sustainable Cross-Linking Approach via Green-Solvent-Based Fenton Reaction

In this study, we present a facile surface modification method using green solvents for a commercial polyimide (PI) nanofiltration membrane to exhibit good acid stability. To enhance acid stability, the PI organic solvent nanofiltration membrane was modified using Fenton's reaction, an oxidative cross-linking process, using environmentally friendly solvents: water and ethanol. The surface properties of the pristine and modified PI membranes were investigated and compared using various analytical tools. We studied the surface morphology using scanning electron microscopy, performed elemental analysis using X-ray photoelectron spectroscopy, investigated chemical bonds using attenuated total reflectance-Fourier transform infrared spectroscopy, and studied thermal stability using thermogravimetric analysis. The acid resistances of the pristine and modified membranes were confirmed through performance tests. The pristine PI nanofiltration membrane exposed to a 50 w/v% sulfuric acid for 4 h showed an increase in the normalized water flux to 205% and a decrease in the MgSO4 normalized rejection to 44%, revealing damage to the membrane. The membrane modified by the Fenton reaction exhibited a decline in flux and improved rejection, which are typical performance changes after surface modification. However, the Fenton-modified membrane exposed to 50 w/v% sulfuric acid for 4 h showed a flux increase of 7% and a rejection increase of 4%, indicating improved acid resistance. Furthermore, the Fenton post-treatment enhanced the thermal stability and organic solvent resistance of the PI membrane. This study shows that the acid resistance of PI membranes can be successfully improved by a novel and facile Fenton reaction using green solvents.

Equilibrium, kinetic and mechanism studies of Cu(II) and Cd(II) ions adsorption by modified chitosan beads

In this study, the Cu(II) and Cd(II) ions removal behavior of crosslinked chitosan beads grafted poly(methacrylamide) (abbreviated as crosslinked chitosan-g-PMAm) from single metal ion solutions was investigated. The modified chitosan beads presented a remarkable improvement in acid resistance. The batch experiments demonstrated that pH of solution played a significant role in adsorption. It was found that the adsorption of Cu(II) and Cd(II) were optimum at pH 4 and pH 5, respectively. The maximum adsorption capacities for Cu(II) and Cd(II) based on Langmuir equation were 140.9 mg g−1 and 178.6 mg g−1, respectively. Pseudo-second order gave a better fit for adsorption data with respect to linearity coefficients than pseudo-first order suggesting that chemisorption or electron transfer is the dominant mechanism of the metal ions onto crosslinked chitosan-g-PMAm. In addition, X-ray photoelectron spectroscopy (XPS) investigations revealed that adsorption of both metal ions took place on the surfaces of crosslinked chitosan-g-PMAm by chelation through CNH2, CO and CO groups. Overall, the modified chitosan has proved a promising adsorbent for removal of metal ions.

Evaluation of MDP and NaF in Two-step Self-etch Adhesives on Enamel Microshear Bond Strength and Morphology of the Adhesive-Enamel Interface.

To evaluate the roles of MDP and NaF in the bonding resin of a two-step self-etch adhesive (2-SEA) on enamel bonding performance. The experimental 2-SEAs were composed of an MDP-containing self-etching primer and four different bonding resins which were MDP- and NaF-free (00), MDP-containing and NaF-free (M0), MDP-free and NaF-containing (0F), and MDP- and NaF-containing (MF) adhesives. Microshear bond strength (µSBS) to enamel and ultimate tensile strength (UTS) of the adhesive resin were determined. The morphological characteristics of the adhesive-enamel interface after acid-base challenge were observed using SEM to evaluate the acid-base resistant zone (ABRZ). No decrease in μSBS was observed even after thermocycling (TC) in 00, 0F and MF. However, the μSBS of M0 significantly decreased after TC. The UTS of M0 significantly decreased after 1- and 180-day storage in water. SEM observations indicated that ABRZ was present in all groups. However, formation of erosion beneath the ABRZ was observed in M0 and 00, whereas formation of a slope without erosion was observed at the bottom of the ABRZ in MF. In the experimental 2-SEAs, the addition of MDP alone to the adhesive resin did not contribute to an improvement in enamel bonding durability and interfacial morphology, whereas the addition of NaF in the adhesive resin demonstrated an enhancement of the bonding durability and improvement of acid resistance at the bonded interface.

Mechanisms and improvement of acid resistance in lactic acid bacteria.

Lactic acid bacteria (LAB) can take advantage of fermentable carbohydrates to produce lactic acid. They are proverbially applied in industry, agricultural production, animal husbandry, food enterprise, pharmaceutical engineering and some other important fields, which are closely related to human life. For performing the probiotic functions, LAB have to face the low pH environment of the gastrointestinal tract. Therefore, acid resistance of LAB is of great importance not only for their own growth, but also for fermentation and preparation of probiotic products. Recent research studies on acid resistance mechanisms of LAB are mainly focused on neutralization process, biofilm and cell density, proton pump, protection of macromolecules, pre-adaptation and cross-protection, and effect of solutes. In this context, biotechnological strategies such as synthetic biology, genome shuffling, high pressure homogenization and adaptive laboratory evolution were also used to improve the acid resistance of LAB to respond to constantly changing low pH environment.

Effects of Pr₆O11 Addition on the Acid Resistance of Ceramic Proppant.

This paper investigated the effect of Pr6O11 addition on the acid resistance of ceramic proppant. Acid resistance of proppants can be improved by introducing Pr6O11 into the Al2O3-CaO-MgO-SiO2 (ACMS) system. To illustrate and explain the mechanism of acid resistance, the samples were characterized by different techniques, using X-ray powder diffraction (XRD) and scanning electron microscopy (SEM). The phase structure of the specimens was characterized by XRD and SEM-detected microstructures of the specimens. It was observed that with the increase of rare-earth oxide content, the acid solubility of the specimens decreased, and then increased when it reached the minimum value 0.45 wt %. The results of the research show that the improvement of acid resistance with rare-earth oxides was achieved by refining the grain size, strengthening the grain boundary, and turning Ca2Al2SiO7, in which acid resistance is poor, into CaAl12O19, which possesses better acid resistance, and then enhance the acid resistance of the proppants. Furthermore, Pr6O11 can form a solid solution with Ca2Al2SiO7 and CaAl12O19. The acid resistance of CaAl12O19 improves with the increase of solid solubility. In contrast, the acid resistance of Ca2Al2SiO7 will decrease after Ca2Al2SiO7 forms a solid solution with Pr6O11.

Early detection of white spot lesions with digital camera and remineralization therapy

In this paper, the characteristics of the early stage of dental caries are discussed and the methods we used to treat the early stage of dental caries to increase the number of caries-free patients are presented. Studies from in vitro to in situ experiments and a clinical study were carried out to support clinical remineralization therapy. To clarify the effect of time for remineralization, the degree of remineralization was assessed at 2 days, 6 days, and 10 days after 2-day demineralization in 0.01 M/L lactic acid buffer (pH 4.0 at 37 degrees ). The remineralization solution contained 3.0 mM/L Ca, 1.8 mM/L P, and 3 ppm fluoride adjusted to pH 7.0. A 10-day continuous remineralization with a 3 ppm fluoride resulted in a high fluoride concentration. To evaluate mineral loss from sound tooth structure and white spot lesions, thin sections (about 90 microm) including white spots (WS) were prepared and exposed to oral conditions for 2 weeks continuously. The mineral loss from sound tooth structure was found to be twice that from WS. In another experiment during the remineralization period, enamel samples were immersed in three different bicarbonate solutions; 0.5, 5.0 and 50 mM/L for 30 minutes, two times per day. Both the bicarbonate and fluoride applied groups showed higher improvement in acid resistance and the amount of remaining mineral was almost two times higher than the controls (p < 0.01). In a clinical study we demonstrated remineralization in patients who followed professional mechanical tooth cleaning and fluoride prophylaxis paste. Using this regime, in patients with deciduous caries present at baseline, over 80 per cent of permanent teeth were caries free at the age of 12 years. In these studies the digital camera with CasMaTCH and an image analysis system showed several advantages for monitoring in de- and remineralization. White spot lesions, rather than intact tooth surfaces, can be mineralized through the daily clinical procedures described in this paper.