In the natural environment, soil pH has an enormous influence on soil biogeochemical processes. Soil pH is, therefore, described as the “master soil variable” that influences myriads of soil biological, chemical, and physical properties and processes that affect plant growth and biomass yield. This paper discusses how soil pH affects processes that are interlinked with the biological, geological, and chemical aspects of the soil environment as well as how these processes, through anthropogenic interventions, induce changes in soil pH. Unlike traditional discussions on the various causes of soil pH, particularly soil acidification, this paper focuses on relationships and effects as far as soil biogeochemistry is concerned. Firstly, the effects of soil pH on substance availability, mobility, and soil biological processes are discussed followed by the biogenic regulation of soil pH. It is concluded that soil pH can broadly be applied in two broad areas, i.e., nutrient cycling and plant nutrition and soil remediation (bioremediation and physicochemical remediation).
Occasionally, the classic understanding of the effect of pH on P uptake from soils is questioned through the claim that maximum P uptake occurs at a pH much lower than 6.5–7. The purpose of this paper was to thoroughly examine that claim and provide a critical review on soil processes that control how soil pH affects P solubility and availability. We discuss how individual P retention mechanisms are affected by pH in isolation and when combined in soils, and how both real and apparent exceptions to the classic view can occasionally occur due to dynamics between mechanisms, experimental techniques (equilibration time, method of soluble P extraction, and pH adjustment), and plant species that thrive under acidic conditions. While real exceptions to the rule of thumb of maximum P availability at near neutral pH can occur, we conclude that the classic textbook recommendation is generally sound.
Soil microorganisms act as gatekeepers for soil–atmosphere carbon exchange by balancing the accumulation and release of soil organic matter. However, poor understanding of the mechanisms responsible hinders the development of effective land management strategies to enhance soil carbon storage. Here we empirically test the link between microbial ecophysiological traits and topsoil carbon content across geographically distributed soils and land use contrasts. We discovered distinct pH controls on microbial mechanisms of carbon accumulation. Land use intensification in low-pH soils that increased the pH above a threshold (~6.2) leads to carbon loss through increased decomposition, following alleviation of acid retardation of microbial growth. However, loss of carbon with intensification in near-neutral pH soils was linked to decreased microbial biomass and reduced growth efficiency that was, in turn, related to trade-offs with stress alleviation and resource acquisition. Thus, less-intensive management practices in near-neutral pH soils have more potential for carbon storage through increased microbial growth efficiency, whereas in acidic soils, microbial growth is a bigger constraint on decomposition rates. Land use intensification could modify microbial activity and thus ecosystem function. Here, Malik et al. sample microbes and carbon-related functions across a land use gradient, demonstrating that microbial biomass and carbon use efficiency are reduced in human-impacted near-neutral pH soils.
This is the first comprehensive review on methods and materials for use in optical sensing of pH values and on applications of such sensors. The Review starts with an introduction that contains subsections on the definition of the pH value, a brief look back on optical methods for sensing of pH, on the effects of ionic strength on pH values and pKa values, on the selectivity, sensitivity, precision, dynamic ranges, and temperature dependence of such sensors. Commonly used optical sensing schemes are covered in a next main chapter, with subsections on methods based on absorptiometry, reflectometry, luminescence, refractive index, surface plasmon resonance, photonic crystals, turbidity, mechanical displacement, interferometry, and solvatochromism. This is followed by sections on absorptiometric and luminescent molecular probes for use pH in sensors. Further large sections cover polymeric hosts and supports, and methods for immobilization of indicator dyes. Further and more specific sections summarize the state of the art in materials with dual functionality (indicator and host), nanomaterials, sensors based on upconversion and 2-photon absorption, multiparameter sensors, imaging, and sensors for extreme pH values. A chapter on the many sensing formats has subsections on planar, fiber optic, evanescent wave, refractive index, surface plasmon resonance and holography based sensor designs, and on distributed sensing. Another section summarizes selected applications in areas, such as medicine, biology, oceanography, bioprocess monitoring, corrosion studies, on the use of pH sensors as transducers in biosensors and chemical sensors, and their integration into flow-injection analyzers, microfluidic devices, and lab-on-a-chip systems. An extra section is devoted to current challenges, with subsections on challenges of general nature and those of specific nature. A concluding section gives an outlook on potential future trends and perspectives.
Abstract Recently, interest in smart packaging, which can show the color change of the packaging film according to the state of the food and evaluate the quality or freshness of the packaged food in real-time, is increasing. As a color indicator, a natural colorant, anthocyanin, drew a lot of attention due to their various colors as well as useful functions properties such as antioxidant activity and anti-carcinogenic and anti-inflammatory effects, prevention of cardiovascular disease, obesity, and diabetes. In particular, the pH-responsive color-changing function of anthocyanins is useful for making color indicator smart packaging films. This review addressed the latest information on the use of natural pigment anthocyanins for intelligent and active food packaging applications. Recent studies on eco-friendly biodegradable polymer-based color indicator films incorporated with anthocyanins have been addressed. Also, studies on the use of smart packaging films to monitor the freshness of foods such as milk, meat, and fish were reviewed. This review highlights the potential and challenges for the use of anthocyanins as pH-responsive color-changing films for intelligent food packaging applications, which may be beneficial for further development of smart color indicator films for practical use.
The pH plays an important physiological role in nature and humans. pH varies from 1 to 8 in human organs with tight regulation in blood and epithelia of barrier organs. The physiological pH of the stratum corneum is 4.1–5.8 and several mechanisms contribute to its formation: filaggrin degradation, fatty acid content, sodium‐hydrogen exchanger (NHE1) activation and melanosome release. First, the acidic pH of the stratum corneum was considered to present an antimicrobial barrier preventing colonization (e.g. by Staphylococcus aureus and Malassezia). Later on, it was found that the pH influences skin barrier function, lipid synthesis and aggregation, epidermal differentiation and desquamation. Enzymes of ceramide metabolism (e.g. β‐glucocerebrosidase or acid sphingomyelinase) as well as proteases (e.g. chymotryptic enzyme or cathepsin D linked to epidermal differentiation and desquamation) are regulated by the pH. Experimental disruption of the physical barrier leads to an increase of pH, returning to normal levels only after many hours. Inflammatory skin diseases and diseases with an involvement of the epidermis exhibit a disturbed skin barrier and an increased pH. This is known for atopic dermatitis, irritant contact dermatitis, ichthyosis, rosacea and acne, but also for aged and dry skin. Normalizing the pH by acidification through topical treatment helps to establish a physiological microbiota, to repair skin barrier, to induce epidermal differentiation and to reduce inflammation.
We present a microkinetic model for CO(2) reduction (CO(2)R) on Cu(211) towards C2 products, based on energetics estimated from an explicit solvent model. We show that the differences in both Tafel slopes and pH dependence for C1 vs C2 activity arise from differences in their multi-step mechanisms. We find the depletion in C2 products observed at high overpotential and high pH to arise from the 2nd order dependence of C-C coupling on CO coverage, which decreases due to competition from the C1 pathway. We further demonstrate that CO(2) reduction at a fixed pH yield similar activities, due to the facile kinetics for CO2 reduction to CO on Cu, which suggests C2 products to be favored for CO2R under alkaline conditions. The mechanistic insights of this work elucidate how reaction conditions can lead to significant enhancements in selectivity and activity towards higher value C2 products. CO2 conversion to reduced products provides a use for greenhouse gases, but reaction complexity stymies mechanistic studies. Here, authors present a microkinetic model for CO2 and CO reduction on copper, based on ab initio simulations, to elucidate pH’s impact on competitive reaction pathways.
Diabetic ulcer is the most common kind of chronic wound worldwide. Though great efforts have been devoted, diabetic ulcer still remains as a challenge that requires constant monitoring and management. In this work, a multifunctional zwitterionic hydrogel is developed to simultaneously detect two fluctuant wound parameters, pH and glucose level, to monitor the diabetic wound status. A pH indicator dye (phenol red) and two glucose sensing enzymes, glucose oxidase (GOx) and horseradish peroxidase (HRP), are encapsulated in the anti‐biofouling and biocompatible zwitterionic poly‐carboxybetaine (PCB) hydrogel matrix. The visible images are collected by a smartphone and transformed into RGB signals to quantify the wound parameters. Results show that the activity and stability of both two enzymes are improved within PCB hydrogel, and the Kcat/Km value of PCB‐HRP is ≈5.5 fold of free HRP in artificial wound exudate. This novel wound dressing can successfully monitor the pH range of 4–8 and glucose level of 0.1–10 × 10−3 m. Meanwhile, it also provides a moist healing environment that can promote diabetic wound healing. This multifunctional wound dressing may open vistas in chronic wound management and guide the diabetes treatment in clinical applications.
Abstract A chitosan-based pH-responsive functional film was prepared by the incorporation of alizarin and its properties were tested for active and intelligent food packaging applications. SEM and FTIR results showed that alizarin was uniformly distributed in the chitosan matrix to form a homogeneous film. The alizarin-added chitosan film showed high UV-blocking property with increased elongation at break, surface hydrophobicity, and thermal stability of the film. The release rate of alizarin from the film was dependent on the solution showing a higher release rate in a 50% ethanol solution than that in water, 10% and 95% ethanol solutions. The synergistic effect of antibacterial activity by the addition of alizarin was negligible against E. coli but slightly increased against L. monocytogenes. However, the antioxidant activity of the chitosan film was significantly increased by the addition of alizarin. The color of the composite film changed vividly from slightly yellow to purple in response to a pH change in the range of 4–10, and the composite film was very sensitive to ammonia vapor. The composite coating could indicate the onset of fish spoilage by showing color change from khaki to light brown as the pH of the packaged fish changed.
Abstract Electrochemical pH sensors are on high demand in numerous applications such as food processing, health monitoring, agriculture and nuclear sectors, and water quality monitoring etc., owing to their fast response (
In the present paper, the authors attempt to explain the importance of pH in soil environment studies and show what mistakes to avoid when measuring pH and interpreting the results obtained. The tests conducted (i.e., extraction in aqua regia, buffer capacity determination, and the impact of acidification on the amount of heavy metals extracted from soils) demonstrated how soil pollution and buffer capacity affect the pace of extracting cadmium (Cd), lead (Pb) and zinc (Zn) cations from heavily polluted and unpolluted soils following gradual acidification. It was shown that soil acidification caused a significant increase in metal mobility in the following order Cd > Zn > Pb and that the highest decrease in pH was observed after adding the first portion of acid. Further addition of acid caused a gradually lower decrease in pH. Soils from the polluted area presented a high buffer capacity. The control samples displayed a distinctly poorer resistance to pH changes in the soil environment. Special focus was placed on cadmium due to its high mobility in soils, even with neutral and slightly alkaline pH. The analyses revealed that in areas heavily polluted by long‐term industrial activity (Igeo > 5 for Zn, Pb and Cd), it is very important to conduct extensive geochemical studies related to the presence and circulation of particularly toxic elements. This is because every environmental factor, especially pH, may significantly affect their mobility, causing metal ions to become more or less active or increasing or decreasing environmental risk related to their presence.
The pH value in the wound milieu plays a key role in cellular processes and cell cycle processes involved in the process of wound healing. Here, a microfluidic assembly technique is employed to fabricate micro‐gel ensembles that can precisely tune the pH value of wound surface and accelerate wound healing. The micro‐gel ensembles consist of poly (hydroxypropyl acrylate‐co‐acrylic acid)‐magnesium ions (poly‐(HPA‐co‐AA)‐Mg2+) gel and carboxymethyl chitosan (CMCS) gel, which can release and absorb hydrogen ion (H+) separately at different stages of healing in response to the evolution of wound microenvironment. By regulating the wound pH to affect the proliferation and migration of cell on the wound and the activity of various biological factors in the wound, the physiological processes are greatly facilitated which results in much accelerated healing of chronic wound. This work presents an effective strategy in designing wound healing materials with vast potentials for chronic wound management.
The complexity of the tumor microenvironment presents significant challenges to cancer therapy, while providing opportunities for targeted drug delivery. Using characteristic signals of the tumor microenvironment, various stimuli-responsive drug delivery systems can be constructed for targeted drug delivery to tumor sites. Among these, the pH is frequently utilized, owing to the pH of the tumor microenvironment being lower than that of blood and healthy tissues. pH-responsive polymer carriers can improve the efficiency of drug delivery in vivo, allow targeted drug delivery, and reduce adverse drug reactions, enabling multifunctional and personalized treatment. pH-responsive polymers have gained increasing interest due to their advantageous properties and potential for applicability in tumor therapy. In this review, recent advances in, and common applications of, pH-responsive polymer nanomaterials for drug delivery in cancer therapy are summarized, with a focus on the different types of pH-responsive polymers. Moreover, the challenges and future applications in this field are prospected.
A number of promising nano-sized particles (nanoparticles) have been developed to conquer the limitations of conventional chemotherapy. One of the most promising methods is stimuli-responsive nanoparticles because they enable the safe delivery of the drugs while controlling their release at the tumor sites. Different intrinsic and extrinsic stimuli can be used to trigger drug release such as temperature, redox, ultrasound, magnetic field, and pH. The intracellular pH of solid tumors is maintained below the extracellular pH. Thus, pH-sensitive nanoparticles are highly efficient in delivering drugs to tumors compared to conventional nanoparticles. This review provides a survey of the different strategies used to develop pH-sensitive nanoparticles used in cancer therapy.
Description Three mechanisms underlie the impact of pH on the activity of electrochemical reactions A promising approach to the sustainable and fossil-free production of fuels and chemicals is the electrochemical conversion of atmospherically available gases such as H2O, CO2, O2, and N2 to fuels and chemicals with renewable electricity (1). Electrocatalysts are essential for practical processes because they increase the reaction rate, efficiency, and selectivity toward desired products. Unfortunately, state-of-the-art electrocatalysts have drawbacks such as the use of precious metals that limit widespread adoption and large overpotentials that lead to very low efficiency. The outstanding challenge is to design and discover active and selective electrocatalysts that are based on earth-abundant materials. It has been understood for decades that the electrolyte pH affects the activity of electrochemical processes. However, the origins of this effect are still under debate.
Recently, Ksenofontov et al (arXiv:2510.03256) observed ambient pressure room-temperature superconductivity in graphite intercalated with lithium-based alloys with transition temperature (according to magnetization measurements) $T_c=330$ $K$. Here, I analyzed the reported temperature dependent resistivity data $ρ(T)$ in these graphite-intercalated samples and found that $ρ(T)$ is well described by the model of two series resistors, where each resistor is described as either an Einstein conductor or a Bloch-Grüneisen conductor. Deduced Einstein and Debye temperatures are $Θ_{E,1} \approx 250$ $K$ and $Θ_{E,2} \approx 1,600$ $K$, and $Θ_{D,1} \approx 300$ $K$ and $Θ_{D,2} \approx 2,200$ $K$, respectively. Following the McMillan formalism, from the deduced $Θ_{E,2}$ and $Θ_{D,2}$, the electron-phonon coupling constant $λ_{e-ph} = 2.2 - 2.6$ was obtained. This value of $λ_{e-ph}$ is approximately equal to the value of $λ_{e-ph}$ in highly compressed superconducting hydrides. Based on this, I can propose that the observed room-temperature superconductivity in intercalated graphite is localized in nanoscale Sr-Ca-Li metallic flakes/particles, which adopt the phonon spectrum from the surrounding bulk graphite matrix, and as a result, conventional electron-phonon superconductivity arises in these nano-flakes/particles at room temperature. Experimental data reported by Ksenofontov et al (arXiv:2510.03256) on trapped magnetic flux decay in intercalated graphite samples supports the proposition.
Deependra K. Ban, Reza Hajian, Matthew Chan
et al.
In high-efficiency smart biomanufacturing, continuous monitoring of products, byproducts, and reagents is crucial for optimizing production processes, improving yield, and ensuring product quality. This monitoring maintains optimal conditions, reduces waste, and enables swift corrective actions, minimizing the risk of producing out-of-specification products. With advancements in cell-free biomanufacturing, the importance of in-line sensing technologies has increased, as they provide real-time tracking of biochemical processes, allowing immediate adjustments to keep manufacturing efficient and consistent. In this study, we successfully developed a graphene field-effect transistor (gFET) sensor to monitor key parameters such as glucose, pH, and immunoglobulin G antibody levels in cell culture media from a CHO cells bioreactor. The gFET sensor accurately detected pH levels between 6.8 and 8.2, glucose concentrations from 5 to 30 mM, and antibody levels ranging from 25 to 100 µg/mL, highlighting the potential of graphene sensors for inline sensing in advanced biomanufacturing.