Amounts of linker missing defects in the UiO-66 crystals synthesized with the addition of Cu2O [53].
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These combined with some of their unique chemistries make them a unique class of chemical and engineering materials. Over the past three decades, porous materials have become one of the research hot spots in the fields of chemistry, physics, and materials science and engineering. The diversity in the pore orientation and dimensionality, combined with the multiplicity in pore shapes and sizes, makes the porous materials highly interested and widely studied. The IUPAC defines the porous materials based on the pore dimensions and classifies them into the microporous materials with pore dimension less than 2 nm, mesoporous materials with pore dimension ranging from 2 to 50 nm, and macroporous materials with pores larger than 50 nm [1].
\nPorous materials have shown great application values in some traditional industries, such as the oil and gas processing, industrial catalysis, adsorption/separation, and fine chemical industries [2, 3, 4, 5]. In more recent decade, they are also being recognized and explored in the research fields of water treatment, sustained release of drugs, and fuel cells, to name a few [6, 7].
\nAmong all porous materials, zeolites are perhaps the most famous microporous materials. In the frameworks of the zeolites, different numbers of TO4 tetrahedral primary structure units connect together to form shared apexes, which enable the creation of the interconnected secondary structure units of various shapes and the formation of the microporous zeolite structure. The “T” in the TO4 tetrahedrons is usually silicon, aluminum, and phosphorus. Chemically, zeolites have adjustable acidity, in addition to their excellent pore channel selectivity and hydrothermal stability. These support the high research value of zeolites in industrial applications such as exchange, adsorption/separation, and petroleum processing. However, the inorganic nature of zeolites limits their adjustability in chemical properties and designability in pore structures and sizes, which restrict the further development and applications of zeolites [2].
\nFor decades, there have been research efforts trying to integrate various metal centres and functional organic molecules into porous structures for the modulation of physical and chemical properties. This effort has resulted in the development of a novel type of hybrid porous crystalline materials formed by the coordination of inorganic metal centres and organic linkers in the 1990s. This new class of porous materials is most commonly known as metal–organic frameworks (MOFs), although they are also sometimes known as porous coordination polymers (PCPs) or inorganic-organic hybrid materials [8, 9, 10]. Ever since their discovery, MOFs have received significant attention from scientists, engineers, and technologists due to their versatilities in structures and chemistries. Since the synthesis of MOFs directly influences the crystallization of the MOF structure, thus dictates its properties and functional performance, extensive work and thousands of research papers have continually emerged focusing on the development of synthesis methods.
\nThe aim of this chapter is to provide an up-to-date overview on the synthesis methods of MOFs reported so far, with the objective to provide empirical guidance for developing synthesis strategy for MOF materials targeting specific properties and functionalities. We draw on our own extensive experiences on modulated synthesis of the UiO-66 MOF material to demonstrate how the crystal morphology and size can be controlled by different modulated synthesis methods, mechanisms of crystallization, and effect of metal doping on MOF crystals during synthesis.
\nAs stated in the introduction, MOFs are a unique class of hybrid porous crystalline materials and have been widely studied over the past two decades for their inherent structure design flexibility and potential applications [11].
\nThe structures of MOFs are constructed by self-assembly between the “nodes” of metal-containing secondary building units (SBUs) and the “bridges” of organic linkers, creating one-, two-, or three-dimensional well-organized network structures with very high pore volumes and surface areas. The framework topologies and pore structures and sizes of MOFs can be designed via selecting various metal centres and organic linkers. Their chemical properties can be modified by chemical functionalization of linkers and post modifications [12, 13, 14].
\nMOFs have extended the chemistry of the porous materials from inorganic to inorganic-organic hybrid. This compositional diversity, combined with the structural diversity, gives them unique properties and functionalities. MOFs are thus a class of highly attractive porous materials for a broad range of applications, including in gas adsorption/separation [15, 16, 17, 18], luminescence and sensing [19, 20, 21, 22], catalysis [23, 24, 25], and others [26, 27, 28, 29].
\nAt their discovery, the method for synthesis of MOFs is solvothermal. Typically, metal precursors and organic linkers are dissolved in solvent and placed in a closed reaction vessel for the formation and self-assembly of MOF crystals. The common solvents used include N,N-dimethylformamide (DMF), N,N-diethylformamide (DEF), methanol, ethanol, and acetonitrile. The synthesis temperature is generally below 220°C, and the crystallization time varies from several hours to several tens of days.
\nAfter more than two decades of research and development, great advances have been made in the synthesis of MOFs. New synthesis methods such as the electrochemical, microwave-assisted, mechanochemical synthesis, microfluidic synthesis method, etc. have all been reported [30]. Figure 1 summarizes the development timeline for the most common synthesis approaches of MOFs [30].
\nTimeline of the most common synthesis approaches for MOFs [
These diverse methods have enabled the synthesis of hundreds of new MOF structures since its first discovery. On top of this, as clearly stated in the principle of “structure dictates function” [31], having the ability to control and tailor the morphology and size and their chemical functionalization of MOF crystals is vital in delivering targeted properties and performances of the resulted MOF materials. This demands the development of more sophisticated synthesis strategies based on the understanding of mechanisms of crystallization occurred during synthesis. The following provides an overview on the currently developed modulated synthesis methods for morphology and size control of MOF crystals and doping to create hybrid MOF crystals.
\nThe synthesis of MOFs involves the process of crystallization during which the nucleation and growth of crystals occur. The nucleation and growth of MOF crystals involve the self-assembly between metal-oxygen clusters and organic linkers. Understanding the influencing factors on the nucleation and growth of MOF crystals during their synthesis will enable accurate controlling of crystal morphology and size. The following discusses the morphology and size development of the MOF crystals during different modulated syntheses.
\nIt is well documented that synthesis conditions, such as temperature, time, solvent type, and reactant concentrations, play important roles in the morphology and size of resulted MOF crystals.
\nFor example, an NH2-MIL-125(Ti) MOF material can be synthesized by a solvothermal method in a mixed solvent of DMF and methanol. Figure 2 shows the SEM images of the NH2-MIL-125(Ti) crystals synthesized with different reactant concentrations, as indicated by the total solvent volumes. By changing the total volume of the solvent alone while maintaining constant ratio between the DMF and methanol and amount of reactants, the morphology of the NH2-MIL-125(Ti) crystals can be modified from circular plates to tetragons and octahedrons [32]. As the crystal morphology changes, the light absorption band of the NH2-MIL-125(Ti) can be tuned from 480 to 533 nm, making it advantageous in photocatalytic applications.
\nSEM images of NH2-MIL-125(Ti) crystals synthesized with different total solvent volumes of (a) 40 mL, (b) 30 mL, (c) 20 mL, (d) 15 mL, (e) 14 mL, and (f) 13.5 mL [
It has been found that the reactant concentration has a significant effect on the deprotonation rate of the organic linkers during the synthesis of NH2-MIL-125(Ti) crystals. The deprotonation rate plays a critical role in the nucleation and growth of the NH2-MIL-125(Ti) crystals. Modulating crystal morphology and size of MOFs by changing the rate of deprotonation is called the deprotonation regulation synthesis [33].
\nBesides changing synthesis conditions, introducing additives during crystallization is another strategy of controlling the morphology and size of MOF crystals. The research lead by Kitagawa first reported the coordination modulation of carboxylic acid additives on the growth of [{Cu2(ndc)2(dabco)}
Coordination modulation method for fabricating [{Cu2(ndc)2(dabco)}
Subsequently, Kitagawa’s group has also synthesized the HKUST-1 crystals using three kinds of monocarboxylic acid additives, the acetic acid, dodecanoic acid, and lauric acid under ultrasonic condition. Figure 4 shows the effect of additive quantity on the morphology of the resulted HKUST-1 crystals. As seen, with the increased additive quantity, not only the size of the HKUST-1 crystals increases from tens of nanometres to several micrometres, the shape of the crystals also changes from cube to octahedron, truncated cube, and tetradecahedron, progressively [35, 36].
\n(a) TEM images of the HKUST-1 crystals obtained with various concentrations of dodecanoic acid and H3BTC; here
It has since been established that the coordination modulation which resulted from using the carboxylic acids has certain universality. It is shown to effectively control the crystal morphology and size of a number of MOFs, including {Cu2(ndc)2(dabco)}
Some surfactants, such as the cetyltrimethylammonium bromide (CTAB) [37] and polyvinylpyrrolidone (PVDF) [38, 39], can also be used for the modulated synthesis of MOFs. In the crystallization of MOF crystals, the surfactant molecules can be selectively absorbed on one or more specific facets of the MOF crystals, thus hinder or alter their growth, and result in the modification of crystal morphology and size.
\nTake the hydrothermal synthesis of ZIF-67 MOF crystals as an example. As shown in Figure 5, by simply changing the amount of CTAB from 0.0025 to 0.025 wt%, a series of the ZIF-67 cubic or rhombic dodecahedron crystals with sizes ranging from ~150 nm to 1 μm can be produced [40]. Additionally, by carbonization of the resulted ZIF-67 crystals in N2 flow, a series of Co-based porous carbon catalysts can be obtained. These Co-based porous carbon catalysts retain the original shape of the ZIF-67 crystals and display an outstanding catalytic performance towards the CO2 methanation at low temperatures.
\nZIF-67 crystals synthesized with different amounts of the CTAB additive (1: 0, 2: 0.0025 wt%, 3: 0.01 wt%, and 4: 0.025 wt%). SEM and TEM images of (a) as-synthesized samples and (b–d) carbonized samples [
It has also been reported that the addition of CTAB can modulate the crystal morphology and size of some other MOFs. Figure 6 shows a number of such examples including IRMOFs [41, 42], HKUST-1 [43], and ZIF-8 [44].
\nThe influence of CTAB additive on the crystal morphology and size of several MOFs. (I) SEM images of IRMOF-3 synthesized with different amounts of CTAB in mg: (a, a1, a2) 0, (b, b1, b2) 5, (c, c1, c2) 8, (d, d1, d2) 12, and (e, e1, e2) 15 [
As one of the most important MOFs, the Zr-BDC (Zr6O4(OH)4(CO2)12) MOF, commonly known as the UiO-66, has been extensively studied due to its high porosity and excellent structural stability at high temperatures and pressures, and excellent stability in chemical (acidic/basic) aggressive environments. The framework of the UiO-66 is built on the [Zr6O4(OH)4] SBUs, each coordinated with 12 1,4-benzene-dicarboxylate (H2BDC) linkers. Figure 7 illustrates the crystal structure of the UiO-66. Its cubic structure is composed of octahedral cages close to 11 Å and tetrahedral cages close to 8 Å, and these cages are connected through narrow triangular windows close to 6 Å [45].
\nSchematic illustration of the UiO-66 structure [
The UiO-66 crystals are commonly synthesized via a solvothermal method at 110–130°C and allowed to crystallize for 24 h. Without modulation, the obtained UiO-66 crystals are usually agglomerates of small cube-like particles of 80–200 nm in size and with low crystallinity. These UiO-66 crystals show low porosity with the BET surface area below 1000 m2 g−1.
\nTo improve the crystallinity of the UiO-66 crystals, carboxylic acid additives have been applied in the synthesis. Schaate et al. first studied the influence of benzoic acid and acetic acid on the crystal growth of the UiO-66 and other Zr-based MOFs [46]. They have found the UiO-66 crystals synthesized are octahedrons of several hundred nanometres in size, as shown in Figure 8. These crystals have a high crystallinity with the BET surface area of up to 1400 m2 g−1. Schaate et al. suggested that the addition of the carboxylic acid additives changes the original coordination equilibrium and thus the crystal growth rate during the crystallization of the UiO-66 crystals. There exists a competition between the coordination of the BDC linkers and carboxylic acid additives towards the Zr6 clusters. This becomes an obstacle for the connection of the BDC linkers and Zr6 clusters, shifting the original coordination equilibrium. This behaviour can be exploited as a way to modulate the morphology and size of the resulted MOF crystals.
\n(a) XRD patterns and (b–d) SEM images of the UiO-66 crystals synthesized with different amounts of benzoic acid additive [
We have been working on precisely controlled synthesis of the UiO-66 and other MOFs with the aim to optimize their properties and extend their application potentials. We were the first to report a hydrofluoric acid (HF) modulated synthesis of the UiO-66 crystals from reactants ZrCl4 and H2BDC [47]. In the study, the amount of HF was varied from 1 eq. to 3 eq., where “eq.” refers to the molar ratio of HF to ZrCl4 in a synthesis batch. A control sample was also synthesized without the addition of HF but under otherwise identical conditions. Figure 9 shows the SEM images of the UiO-66 crystals synthesized. As seen, the addition of the HF facilitates growth of the UiO-66 crystals with the mean size of the crystals increasing from ~150 nm to 7 μm with increased HF addition. By controlling the concentration of the reactants, the morphology of crystals changed from truncated cube to cuboctahedron.
\nSEM images of the UiO-66 crystals synthesized with different amounts of HF additive and changing concentrations of the reactants. At CZr = BDC = 13.6 mM, (a) HF = 1 eq., (b) HF = 2 eq., and (c) HF = 3 eq. At CZr = BDC = 18.2 mM, (d) HF = 1 eq., (e) HF = 2 eq., and (f) HF = 3 eq. At CZr = BDC = 27.2 mM, (g) HF = 1 eq., (h) HF = 2 eq., and (i) HF = 3 eq. [
To understand the impact of the HF additive, elemental mapping and 19F NMR analysis of the resulted UiO-66 crystals were conducted.
\n\nFigure 10 shows the EDS mapping of the synthesized UiO-66 crystals. As seen, without the addition of HF, a small amount of Cl was detected in the crystals even after heat treatment up to 300°C. This somewhat unexpected observation of the Cl is believed to be resulted from structure defects in the synthesized UiO-66 crystals. It is known that the UiO-66 crystal structure contains defects in the form of missing linkers, which would result in an unsaturated framework. To compensate for this charge imbalance of the framework, negatively charged Cl ions (from the ZrCl4 reactant) are “needed” to coordinate with the defective sites.
\nEDS maps of the UiO-66 crystals synthesized (a) without HF additive, (b) with 3 eq. HF additive, and (c) with 3 eq. HF additive and then heat-treated at 150°C [
For the crystals synthesized with the addition of HF, EDS analysis of the crystals revealed noticeable F in the crystals, with no Cl observed. This indicates that, in the presence of stronger electronegative F, the F ions now coordinate to the linker defective sites instead of chlorine ions in the SBUs of the UiO-66 crystals.
\nThis mechanism was further supported by the 19F NMR spectra shown in Figure 11. As seen, the spectrum of 3F-UiO-66 heat-treated at 150°C (curve a) contains a strong signal of two partially overlapped peaks cantered at −155 ppm and −156 ppm. These peaks are assigned to the F bonded directly to Zr in the SBUs and the F physisorbed, respectively. When the 3F-UiO-66 is heat-treated at 300°C, as seen in curve (b), the peak at −155 ppm becomes stronger and narrower, whereas the peak at −156 ppm disappears. It indicates that F remains bonded to the Zr in the 3F-UiO-66 framework even after being heat-treated up to 300°C.
\n\n19F NMR spectra of the 3F-UiO-66 crystals heat-treated at (a) 150°C and (b) 300°C. The asterisks indicate the spinning sidebands [
The thermostability of the UiO-66 crystals was enhanced after the introduction of fluorine in the framework structure. Figure 12 shows the TGA curves of the UiO-66 crystals synthesized with different amounts of HF additive. The significant weight loss event observed at ~500°C represents the complete decomposition of the UiO-66 framework. It can be seen that the F introduction has stabilized the framework, as indicated by the progressively increased decomposition temperature. This is attributed to the higher coordination strength of Zr▬F in the fluorine-involved crystals than the Zr▬Cl or Zr▬O in the fluorine-free crystals, resulting in the stabilization of framework structure of the fluorine-involved UiO-66.
\nTGA curves of the UiO-66 crystals synthesized with different amounts of HF additive (C = 18.2 mM) [
Furthermore, as the UiO-66 crystals were modulated from small cube-like morphology to micron-sized cuboctahedron morphology with the addition of the HF during synthesis, their porosity increases [47]. Figure 13 displays the Ar sorption–desorption isotherms and pore size distributions of the parent and fluorine-involved crystals. As seen, the 3 fluorine-involved crystals (samples c, f, and i in Figure 9) exhibit significantly higher Ar adsorption values than the parent crystals synthesized without HF, and the pore size distributions show the enhanced porosity of the fluorine-involved crystals.
\n(a) Ar sorption-desorption isotherms and (b) pore size distributions of the synthesized UiO-66 with various crystal sizes and morphologies [
In more recent years, nanosized MOFs (also known as nMOFs or NMOFs) have attracted great attentions. nMOFs have short diffusion lengths and high specific surface areas, both are of critical importance in catalysis and sorption, especially in liquid-phase applications [34, 48]. In addition, nMOFs are highly desirable for porous membranes [49, 50], thin film devices [51], and medical applications [52].
\nWe have reported a novel method for the modulated synthesis of nUiO-66 crystals, in which a new type of additive, solid Cu2O, was used to mediate the synthesis [53]. Figure 14 shows the TEM images of the UiO-66 crystals synthesized with different amounts of Cu2O additive. As illustrated, by increasing the amount of Cu2O additive, the mean sizes of the UiO-66 crystals reduce progressively from ~265 to 40 nm. The crystals maintain an octahedral morphology until when the crystal size is too small to display distinguishable facets and thus appear as spherical particles. The synthesized nano UiO-66 crystals were found to be chemically pure without the contamination of Cu. They have high BET surface area of more than 1100 m2 g−1 and contain rich porosity. Figure 15 shows the Ar sorption isotherms and pore size distributions of the UiO-66 crystals. Although the amount of micropores between 6 Å and 10 Å decreased gradually with the decreasing crystal size, noticeable quantity of mesopores of 10–30 nm became prevailed, demonstrating the dual micro- and mesoporosity of the nano UiO-66 crystals.
\nTEM images of the UiO-66 crystals synthesized with different amounts of Cu2O additive. Here the molar ratio R =
(a) Ar sorption isotherms and (b) pore size distributions (measured between 0 and 50 nm) of the UiO-66 crystals synthesized with different amounts of Cu2O additive. Here the molar ratio R =
During the Cu2O-modulated synthesis, the added solid Cu2O was observed to dissolve gradually in the mother liquor, resulting in the formation of a pale orange-colored solution. Figure 16 shows the far infrared (FIR) spectra of solid Cu2O and a number of mixed solutions relevant to the synthesis. As illustrated in the inset of the figure, solid Cu2O shows the Cu▬O absorption band at 138 cm−1. Upon the addition of solid Cu2O in DMF, the Cu▬O bond shifts to 143 cm−1 as seen in spectrum b. When the ZrCl4 was added to the suspension of the Cu2O and DMF, the FIR spectrum (c) shows dramatically decreased Cu▬O adsorption band accompanied by the arrival of an intense adsorption band at 113 cm−1. This new band can be ascribed to a shifted stretching vibration of Cu▬Cl bonds, which are usually at 109 cm−1 for the anionic [CuCl2]− complex [54]. The FIR analysis seems to suggest that the dissolution of Cu2O in the precursor solution of the UiO-66 is driven by the formation of the [Cu▬Cl] complexes.
\nFar-IR spectra of the solid Cu2O and a number of mixtures relevant to the UiO-66 synthesis, where the molar ratio of Cu/ZrCl4 is 1.2. (a) ZrCl4/DMF solution, (b) Cu2O/DMF suspension, and (c) ZrCl4 + Cu2O/DMF solution. The inset is for solid Cu2O [
It has also been found [53] that the amount of ZrCl4 in the Cu2O-modulated synthesis plays a crucial role in the growth of the UiO-66 crystals. The higher the concentration of the ZrCl4, the weaker the Cu2O’s impact on the crystal growth and thus benefits the formation of large size UiO-66 crystals. In contrast, decreasing the concentration of the ZrCl4 favors the production of small UiO-66 crystals, which also accompanied with the loss of crystallinity. It is thus believed that the [Cu▬Cl] complex is capable of coordinating with the Zr4+, leading to a decreased coordination of the Zr6 clusters with BDC linkers, preventing crystal growth.
\nAdditionally, under the modulation of Cu2O additive, the synthesized UiO-66 crystals not only have reduced sizes, but also enriched structure defects [53]. Both the XRD and TGA analyses of the nano UiO-66 crystals indicate the existence of linker defects and metal cluster defects. Table 1 presents quantified amounts of the linker missing defects in the synthesized nano UiO-66 crystals. It is seen that the number of linker defects increases with the decreasing crystal size, revealing a more open framework of the nano UiO-66.
\nIn recent years, there have been many reports on the structural defects of the UiO-66 crystals [55, 56, 57, 58, 59, 60]. These structural defects are found to relate strongly to the structure stability, adsorption, and catalysts performance of the UiO-66 material.
\nHere R represents the molar ratio of Cu/ZrCl4, and x is the number of linker missing defects. The formula represents the defective molecular formula of the UiO-66 crystals, and Zr6O6(BDC)6 is the formula of a defect-free dehydroxylated UiO-66.
\nIntroducing foreign metal centres into the framework structure to obtain hybrid (i.e. mixed metal) MOFs is a strategy for developing novel MOFs. We have explored the possibility of facile synthesis of Ti4+-doped hybrid UiO-66-
Sample | \nAverage crystal size of the synthesize nano UiO-66/nm | \nR | \nCu2O addition | \n|
---|---|---|---|---|
x | \nFormula | \n|||
1a | \n265 | \n0 | \n0.42 | \nZr6O6.42(BDC)5.58\n | \n
1b | \n155 | \n0.2 | \n0.50 | \nZr6O6.50(BDC)5.50\n | \n
1c | \n96 | \n0.5 | \n0.84 | \nZr6O6.84(BDC)5.16\n | \n
1d | \n75 | \n1.0 | \n0.84 | \nZr6O6.84(BDC)5.16\n | \n
1e | \n48 | \n1.2 | \n0.84 | \nZr6O6.84(BDC)5.16\n | \n
1f | \n40 | \n1.5 | \n1.05 | \nZr6O7.05(BDC)4.95\n | \n
Amounts of linker missing defects in the UiO-66 crystals synthesized with the addition of Cu2O [53].
\nFigure 17 shows the SEM images and EDS elemental mapping of the synthesized UiO-66-
SEM images of the UiO-66-
\nFigure 18 shows the FT-IR spectra of the parent UiO-66 and doped UiO-66-
FT-IR spectra of the parent UiO-66, doped UiO-66-
\nFigure 19 shows the EXAFS spectra of the parent UiO-66 and doped UiO-66-2.7Ti crystals. It further demonstrates the alternation in coordination state around the Zr4+ caused by the Ti4+ doping. As seen, the peak at ~1.7 Å that relates to the Zr▬O bonds shifts to 1.6 Å after Ti4+ doping. Additionally, the peak at around 3.0 Å that represents the Zr⋯Zr bonds connecting through the Oμ3-O or Oμ3-OH decreases noticeably after doping, likely due to the formation of Zr⋯Ti coordination.
\nEXAFS spectra of the parent UiO-66 and the UiO-66-2.7Ti crystals [
The synthesized UiO-66-
MOFs, with their inherent high surface areas, uniform, versatile, and tuneable pores, and tailorable physicochemical properties, have been projected to have a broad range of potential applications in various areas. Since the discovery of the first MOF structure in the 1990s, hundreds of new MOFs have been synthesized successfully.
\nIn the past two decades, much attention has been paid to develop methods to control the morphology and size of MOF crystals, in order to tailor the structure properties and performance of MOF materials. Such research efforts have resulted in the development of effective synthesis methods which are capable of modulation of morphology and size of MOF crystals through different mechanisms, including the deprotonation regulation, coordination modulation, and surfactant modulation synthesis. This review chapter has highlighted a number of successful synthesis routes using, for example, the carboxylic acids, HF, and solid Cu2O additives to modulate the MOF crystal formation and growth. It has also demonstrated the ability of doping to create hybrid MOFs with improved properties and functionalities.
\nIt remains a significant challenge on how to best fully utilize the unique set of properties and functionalities of the chemically versatile MOFs and realize their application potentials in various identified areas. While there have been significant achievements on the structure optimization and performance development of MOFs to date, it is anticipated that further progress can be made with more fundamental research and industrial application of MOFs.
\nThis work was supported by the National Natural Science Foundation of China (Grant no. 21236008).
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In the ecological niche, the appearance of organisms is affected by anthropogenic and non-anthropogenic environmental factors. Algae composition and temporal variation in abundances are important in determining the trophic level of lakes. Algal communities are sensitive to changes in their habitat, and thus, total biomass of algae and many algae species are used as indicators of water quality. Algae communities give more knowledge on variations in water quality than nutrient or chlorophyll-a values. Water quality is a canonical group of physical, chemical, and biological properties of the given water. Consequently, eutrophication of freshwater is regarded as a water quality which results in the degeneration of the aquatic ecosystem and affects water utilisation. Cyanobacteria has been accepted as a major indicator of eutrophication in freshwater as their blooms are common in waters affected by nutrient concentration. The purpose of this chapter is to assess physical and chemical variables and the role of algal abundance to determine the water quality in the freshwater ecosystems.",book:{id:"5128",slug:"algae-organisms-for-imminent-biotechnology",title:"Algae",fullTitle:"Algae - Organisms for Imminent Biotechnology"},signatures:"Didem Gökçe",authors:[{id:"178260",title:"Associate Prof.",name:"Didem",middleName:null,surname:"Gokce",slug:"didem-gokce",fullName:"Didem Gokce"}]},{id:"50534",doi:"10.5772/63069",title:"Considerations for Photobioreactor Design and Operation for Mass Cultivation of Microalgae",slug:"considerations-for-photobioreactor-design-and-operation-for-mass-cultivation-of-microalgae",totalDownloads:5994,totalCrossrefCites:8,totalDimensionsCites:17,abstract:"Microalgae have great biotechnological potential for production of substances through photosynthesis. Light capture process and electron transportation imply energy losses due to reflection, fluorescence emission, and energy dissipation as heat, giving a maximum theoretical value of 8‐9% for microalgae energy capture efficiency and conversion to biomass. For development of full potential of microalgae the knowledge of the light capture process is required. High yields can only be obtained linking photobioreactor design with biological process taking place inside. In massive microalgae cultures, light gradients are generated and this depends on the biomass concentration, cellular types, cells sizes, and pigment content, and also on geometry, hydrodynamic, and light conditions inside the photobioreactor. In the present chapter we explain the relationship between light energy capture process and photobioreactor design and operation conditions, like turbulence, gas exchange, and nutrient requirements. Finally, the productivity and costs are discussed, and the parameters that determine the economic viability of any microalgae culture.",book:{id:"5128",slug:"algae-organisms-for-imminent-biotechnology",title:"Algae",fullTitle:"Algae - Organisms for Imminent Biotechnology"},signatures:"Juan Cristóbal García Cañedo and Gema Lorena López Lizárraga",authors:[{id:"185868",title:"Dr.",name:"Gema Lorena",middleName:null,surname:"López-Lizárraga",slug:"gema-lorena-lopez-lizarraga",fullName:"Gema Lorena López-Lizárraga"},{id:"293413",title:"Dr.",name:"Juan Cristóbal",middleName:null,surname:"García Cañedo",slug:"juan-cristobal-garcia-canedo",fullName:"Juan Cristóbal García Cañedo"}]},{id:"69201",doi:"10.5772/intechopen.89324",title:"Drying and Quality of Microalgal Powders for Human Alimentation",slug:"drying-and-quality-of-microalgal-powders-for-human-alimentation",totalDownloads:1263,totalCrossrefCites:5,totalDimensionsCites:15,abstract:"The demand for natural foods with high protein content and functional properties is constantly growing in the last years. In this context, microalgae as Spirulina (Arthrospira spp.), Chlorella spp., Haematococcus pluvialis, Dunaliella salina, and others, assume a key role to diversify the offer of nutritious and functional ingredients and supplements. Microalgae are commercialized, mostly, as dried powders to facilitate their use as food ingredients and to allow easy transportation and long-term stability. Microalgal powder quality and storage stability depend mainly on drying method, packaging, and storage conditions. Most of the studies that approach the subject of microalgal drying evaluate the efficiency of the process and suitability for this raw material. However, studies that assess the effect of traditional and innovative drying methods on quality of microalgal powder for human consumption are rare in literature. In this chapter, the state of the art of drying processing technology for microalgae was reviewed, discussing the effect of dehydration on quality and stability of microalgal powders with potential use in human alimentation.",book:{id:"9354",slug:"microalgae-from-physiology-to-application",title:"Microalgae",fullTitle:"Microalgae - From Physiology to Application"},signatures:"Fábio de Farias Neves, Mariana Demarco and Giustino Tribuzi",authors:null},{id:"50671",doi:"10.5772/63272",title:"Challenges and Opportunities in the Present Era of Marine Algal Applications",slug:"challenges-and-opportunities-in-the-present-era-of-marine-algal-applications",totalDownloads:2747,totalCrossrefCites:3,totalDimensionsCites:12,abstract:"Marine algae are of high importance in their natural habitats and even more now in the world of green technology. The sprouting interest of the scientific community and industries in these organisms is driven by the fast-growing world of modern biotechnology. Genomics, transcriptomics, proteomics, metabolomics and their integration collectively termed here as ‘marine algal-omics’ have broadened the research horizon in view of enhancing human’s life by addressing environmental problems and encouraging novelty in the field of pharmaceuticals among so many more. Their use in the human society dates back to 500 B. C. in China and later across the globe; they are still being used for similar purposes and more today. There is a hiking interest in marine algae and their derivatives—from phycoremediation, food supplements, pharmaceuticals to dyes. Marine algae are currently considered as an emerging panacea for the society. They are being studied in a multitude of arenas. The multi-use of marine algae is enticing and promises to be a boon for industrial applications. Yet, most marine algae face challenges that might variably constrain their commercialisation. This chapter gives an overview of marine algae including all the ‘omics’ technologies involved in studying marine algae and it explores their multitude applications. It also draws the various successful industries budded around them and presents some of the challenges and opportunities along with future directions.",book:{id:"5128",slug:"algae-organisms-for-imminent-biotechnology",title:"Algae",fullTitle:"Algae - Organisms for Imminent Biotechnology"},signatures:"Keshini Beetul, Arvind Gopeechund, Deepeeka Kaullysing, Sushma\nMattan-Moorgawa, Daneshwar Puchooa and Ranjeet Bhagooli",authors:[{id:"178209",title:"Ms.",name:"Keshini",middleName:null,surname:"Beetul",slug:"keshini-beetul",fullName:"Keshini Beetul"},{id:"184390",title:"Mr.",name:"Arvind",middleName:null,surname:"Gopeechund",slug:"arvind-gopeechund",fullName:"Arvind Gopeechund"},{id:"184391",title:"Ms.",name:"Deepeeka",middleName:null,surname:"Kaullysing",slug:"deepeeka-kaullysing",fullName:"Deepeeka Kaullysing"},{id:"184392",title:"Mrs.",name:"Sushma",middleName:null,surname:"Mattan-Moorgawa",slug:"sushma-mattan-moorgawa",fullName:"Sushma Mattan-Moorgawa"},{id:"184393",title:"Prof.",name:"Daneshwar",middleName:null,surname:"Puchooa",slug:"daneshwar-puchooa",fullName:"Daneshwar Puchooa"},{id:"184394",title:"Dr.",name:"Ranjeet",middleName:null,surname:"Bhagooli",slug:"ranjeet-bhagooli",fullName:"Ranjeet Bhagooli"}]}],mostDownloadedChaptersLast30Days:[{id:"64156",title:"Cyanobacteria Growth Kinetics",slug:"cyanobacteria-growth-kinetics",totalDownloads:1799,totalCrossrefCites:2,totalDimensionsCites:5,abstract:"Harmful cyanobacterial blooms are a global problem for freshwater ecosystems used for drinking water supply and recreational purposes. Cyanobacteria also produce a wide variety of toxic secondary metabolites, called cyanotoxins. High water temperatures have been known to lead to cyanobacterial bloom development in temperate and semiarid regions. Increased temperatures as a result of climate change could therefore favor the growth of cyanobacteria, thus augmenting the risks associated with the blooms. Though temperature is the main factor affecting the growth kinetics of bacteria, the availability of nutrients such as nitrogen and phosphorus also plays a significant role. This chapter studies the growth kinetics of toxin-producing Microcystis aeruginosa and evaluates potential risks to the population in scenarios of climate change and the presence of nutrients. The most suitable control methods for mitigation are also evaluated.",book:{id:"6889",slug:"algae",title:"Algae",fullTitle:"Algae"},signatures:"Leda Giannuzzi",authors:[{id:"252117",title:"Dr.",name:"Leda",middleName:null,surname:"Giannuzzi",slug:"leda-giannuzzi",fullName:"Leda Giannuzzi"}]},{id:"65952",title:"CO2 Capture for Industries by Algae",slug:"co-sub-2-sub-capture-for-industries-by-algae",totalDownloads:2102,totalCrossrefCites:5,totalDimensionsCites:11,abstract:"The increased usage of fossil fuels has led to increase in the concentration of CO2, which is a greenhouse gas responsible for global warming. Algae-based CO2 conversion is a cost-effective option for reducing carbon footprint. In addition, algae-based CO2 mitigation strategy has the potential to obtain valuable products at the end of the process. In the present study, freshwater algal species were isolated and identified for CO2 capture, such as Hydrodictyon, Spirogyra, Oscillatoria, Oedogonium, and Chlorella. The algal strains were screened based on different parameters like fast growth rate, high rate of photosynthesis, strong tolerance to the trace constituents of other gases (gaseous hydrocarbons, NOx, SOx, etc.), high temperature tolerance, and possibility to produce high value products, etc. The study involves integrated methods for utilizing 90–99% CO2 from a natural gas processing industry (GAIL India, Ltd.) as well as 13–15% of CO2 from flue gas of thermal power plants (Chandrapura and Santaldih Thermal Power Station) as carbon nutrient source along with the additional nutritional supplements. A 400-ml and 25-l flat panel photo-bioreactor (PSI Photo-bioreactors) was used for CO2 capture. After CO2 capture, the algal biomass was used to extract value-added products such as amino acid rich feed, algal oil, algal pellets, etc.",book:{id:"6889",slug:"algae",title:"Algae",fullTitle:"Algae"},signatures:"Vetrivel Anguselvi, Reginald Ebhin Masto, Ashis Mukherjee and Pradeep Kumar Singh",authors:[{id:"255851",title:"Dr.",name:"Vetrivel",middleName:null,surname:"Anguselvi",slug:"vetrivel-anguselvi",fullName:"Vetrivel Anguselvi"},{id:"269996",title:"Dr.",name:"R E",middleName:null,surname:"Masto",slug:"r-e-masto",fullName:"R E Masto"},{id:"269997",title:"Dr.",name:"Ashis",middleName:null,surname:"Mukherjee",slug:"ashis-mukherjee",fullName:"Ashis Mukherjee"},{id:"270059",title:"Dr.",name:"P K",middleName:null,surname:"Singh",slug:"p-k-singh",fullName:"P K Singh"}]},{id:"51074",title:"Algae as an Indicator of Water Quality",slug:"algae-as-an-indicator-of-water-quality",totalDownloads:5034,totalCrossrefCites:11,totalDimensionsCites:23,abstract:"The formation of plankton/algae under natural conditions is related to tolerance class (ecological optimum) due to abiotic limiting factors of ecosystem, as well as the biotic interactions among algae. In the ecological niche, the appearance of organisms is affected by anthropogenic and non-anthropogenic environmental factors. Algae composition and temporal variation in abundances are important in determining the trophic level of lakes. Algal communities are sensitive to changes in their habitat, and thus, total biomass of algae and many algae species are used as indicators of water quality. Algae communities give more knowledge on variations in water quality than nutrient or chlorophyll-a values. Water quality is a canonical group of physical, chemical, and biological properties of the given water. Consequently, eutrophication of freshwater is regarded as a water quality which results in the degeneration of the aquatic ecosystem and affects water utilisation. Cyanobacteria has been accepted as a major indicator of eutrophication in freshwater as their blooms are common in waters affected by nutrient concentration. The purpose of this chapter is to assess physical and chemical variables and the role of algal abundance to determine the water quality in the freshwater ecosystems.",book:{id:"5128",slug:"algae-organisms-for-imminent-biotechnology",title:"Algae",fullTitle:"Algae - Organisms for Imminent Biotechnology"},signatures:"Didem Gökçe",authors:[{id:"178260",title:"Associate Prof.",name:"Didem",middleName:null,surname:"Gokce",slug:"didem-gokce",fullName:"Didem Gokce"}]},{id:"64455",title:"Cyanobacteria for PHB Bioplastics Production: A Review",slug:"cyanobacteria-for-phb-bioplastics-production-a-review",totalDownloads:2186,totalCrossrefCites:4,totalDimensionsCites:11,abstract:"Cyanobacteria, or blue-green algae, can be used as host to produce polyhydroxyalkanoates (PHA), which are promising bioplastic raw materials. The most important material thereof is polyhydroxybutyrate (PHB), which can replace the commodity polymer polypropylene (PP) in many applications, yielding a bio-based, biodegradable alternative solution. The advantage from using cyanobacteria to make PHB over the standard fermentation processes, with sugar or other organic (waste) materials as feedstock, is that the sustainability is better (compare first-generation biofuels with the feed vs. fuel debate), with CO2 being the only carbon source and sunlight being the sole energy source. In this review article, the state of the art of cyanobacterial PHB production and its outlook is discussed. Thirty-seven percent of dry cell weight of PHB could be obtained in 2018, which is getting close to up to 78% of PHB dry cell weight in heterotrophic microorganisms in fermentation reactors. A good potential for cyanobacterial PHB is seen throughout the literature.",book:{id:"6889",slug:"algae",title:"Algae",fullTitle:"Algae"},signatures:"Erich Markl, Hannes Grünbichler and Maximilian Lackner",authors:[{id:"251081",title:"Dr.",name:"Maximilian",middleName:null,surname:"Lackner",slug:"maximilian-lackner",fullName:"Maximilian Lackner"},{id:"255232",title:"Prof.",name:"Erich",middleName:null,surname:"Markl",slug:"erich-markl",fullName:"Erich Markl"},{id:"277237",title:"Dr.",name:"Hannes",middleName:null,surname:"Grünbichler",slug:"hannes-grunbichler",fullName:"Hannes Grünbichler"}]},{id:"50544",title:"Algal Nanoparticles: Synthesis and Biotechnological Potentials",slug:"algal-nanoparticles-synthesis-and-biotechnological-potentials",totalDownloads:5784,totalCrossrefCites:17,totalDimensionsCites:67,abstract:"A nanoparticle can be defined as a small object that behaves as a whole unit in terms of its transport and properties. Nanoparticles are sized between 1 and 100 nm in diameter. Nanoparticles can act against the microbes in multiple ways, and the microbes are less likely to develop resistance against nanoparticles because it requires multiple gene mutations. The large surface-to-volume ratio of nanoparticles, their ability to easily interact with other particles, and several other features make them attractive tools in various fields. Nanoparticles are widely used various fields such as electronics, cosmetics, biomedical, and biotechnology. Nanoparticles can be synthesized by physical methods such as attrition, pyrolysis, and using some wet chemical methods. The physical and chemical methods have various drawbacks such as high cost of production, require high energy input and generation of toxic by-products. To overcome this, several biological methods are employed in the synthesis of nanoparticles. The biological methods are generally cost effective, nontoxic, and ecofriendly. This chapter focuses on the methods involved in algal-synthesized nanoparticles and its applications.",book:{id:"5128",slug:"algae-organisms-for-imminent-biotechnology",title:"Algae",fullTitle:"Algae - Organisms for Imminent Biotechnology"},signatures:"Felix LewisOscar, Sasikumar Vismaya, Manivel Arunkumar,\nNooruddin Thajuddin, Dharumadurai Dhanasekaran and Chari\nNithya",authors:[{id:"183668",title:"Dr.",name:"Nithya",middleName:null,surname:"Chari",slug:"nithya-chari",fullName:"Nithya Chari"}]}],onlineFirstChaptersFilter:{topicId:"424",limit:6,offset:0},onlineFirstChaptersCollection:[],onlineFirstChaptersTotal:0},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:0,limit:8,total:null},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:9,numberOfPublishedChapters:87,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:98,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:27,numberOfPublishedChapters:287,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:9,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:11,numberOfPublishedChapters:139,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:8,numberOfPublishedChapters:129,numberOfOpenTopics:0,numberOfUpcomingTopics:2,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!1},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:107,numberOfOpenTopics:3,numberOfUpcomingTopics:1,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:10,numberOfPublishedChapters:103,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:12,numberOfOpenTopics:2,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:0,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!1},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:0,numberOfPublishedChapters:10,numberOfOpenTopics:4,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. The whole process of submitting an article and editing of the submitted article goes extremely smooth and fast, the number of reads and downloads of chapters is high, and the contributions are also frequently cited.",author:{id:"55578",name:"Antonio",surname:"Jurado-Navas",institutionString:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRisIQAS/Profile_Picture_1626166543950",slug:"antonio-jurado-navas",institution:{id:"720",name:"University of Malaga",country:{id:null,name:"Spain"}}}},{id:"6",text:"It is great to work with the IntechOpen to produce a worthwhile collection of research that also becomes a great educational resource and guide for future research endeavors.",author:{id:"259298",name:"Edward",surname:"Narayan",institutionString:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",slug:"edward-narayan",institution:{id:"3",name:"University of Queensland",country:{id:null,name:"Australia"}}}}]},series:{item:{id:"10",title:"Physiology",doi:"10.5772/intechopen.72796",issn:"2631-8261",scope:"Modern physiology requires a comprehensive understanding of the integration of tissues and organs throughout the mammalian body, including the cooperation between structure and function at the cellular and molecular levels governed by gene and protein expression. While a daunting task, learning is facilitated by identifying common and effective signaling pathways mediated by a variety of factors employed by nature to preserve and sustain homeostatic life. \r\nAs a leading example, the cellular interaction between intracellular concentration of Ca+2 increases, and changes in plasma membrane potential is integral for coordinating blood flow, governing the exocytosis of neurotransmitters, and modulating gene expression and cell effector secretory functions. Furthermore, in this manner, understanding the systemic interaction between the cardiovascular and nervous systems has become more important than ever as human populations' life prolongation, aging and mechanisms of cellular oxidative signaling are utilised for sustaining life. \r\nAltogether, physiological research enables our identification of distinct and precise points of transition from health to the development of multimorbidity throughout the inevitable aging disorders (e.g., diabetes, hypertension, chronic kidney disease, heart failure, peptic ulcer, inflammatory bowel disease, age-related macular degeneration, cancer). With consideration of all organ systems (e.g., brain, heart, lung, gut, skeletal and smooth muscle, liver, pancreas, kidney, eye) and the interactions thereof, this Physiology Series will address the goals of resolving (1) Aging physiology and chronic disease progression (2) Examination of key cellular pathways as they relate to calcium, oxidative stress, and electrical signaling, and (3) how changes in plasma membrane produced by lipid peroxidation products can affect aging physiology, covering new research in the area of cell, human, plant and animal physiology.",coverUrl:"https://cdn.intechopen.com/series/covers/10.jpg",latestPublicationDate:"May 14th, 2022",hasOnlineFirst:!0,numberOfPublishedBooks:11,editor:{id:"35854",title:"Prof.",name:"Tomasz",middleName:null,surname:"Brzozowski",slug:"tomasz-brzozowski",fullName:"Tomasz Brzozowski",profilePictureURL:"https://mts.intechopen.com/storage/users/35854/images/system/35854.jpg",biography:"Prof. Dr. Thomas Brzozowski works as a professor of Human Physiology and is currently Chairman at the Department of Physiology and is V-Dean of the Medical Faculty at Jagiellonian University Medical College, Cracow, Poland. His primary area of interest is physiology and pathophysiology of the gastrointestinal (GI) tract, with the major focus on the mechanism of GI mucosal defense, protection, and ulcer healing. He was a postdoctoral NIH fellow at the University of California and the Gastroenterology VA Medical Center, Irvine, Long Beach, CA, USA, and at the Gastroenterology Clinics Erlangen-Nuremberg and Munster in Germany. He has published 290 original articles in some of the most prestigious scientific journals and seven book chapters on the pathophysiology of the GI tract, gastroprotection, ulcer healing, drug therapy of peptic ulcers, hormonal regulation of the gut, and inflammatory bowel disease.",institutionString:null,institution:{name:"Jagiellonian University",institutionURL:null,country:{name:"Poland"}}},editorTwo:null,editorThree:null},subseries:{paginationCount:4,paginationItems:[{id:"10",title:"Animal Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/10.jpg",isOpenForSubmission:!0,annualVolume:11406,editor:{id:"202192",title:"Dr.",name:"Catrin",middleName:null,surname:"Rutland",slug:"catrin-rutland",fullName:"Catrin Rutland",profilePictureURL:"https://mts.intechopen.com/storage/users/202192/images/system/202192.png",biography:"Catrin Rutland is an Associate Professor of Anatomy and Developmental Genetics at the University of Nottingham, UK. She obtained a BSc from the University of Derby, England, a master’s degree from Technische Universität München, Germany, and a Ph.D. from the University of Nottingham. She undertook a post-doctoral research fellowship in the School of Medicine before accepting tenure in Veterinary Medicine and Science. Dr. Rutland also obtained an MMedSci (Medical Education) and a Postgraduate Certificate in Higher Education (PGCHE). She is the author of more than sixty peer-reviewed journal articles, twelve books/book chapters, and more than 100 research abstracts in cardiovascular biology and oncology. She is a board member of the European Association of Veterinary Anatomists, Fellow of the Anatomical Society, and Senior Fellow of the Higher Education Academy. Dr. Rutland has also written popular science books for the public. https://orcid.org/0000-0002-2009-4898. www.nottingham.ac.uk/vet/people/catrin.rutland",institutionString:null,institution:{name:"University of Nottingham",institutionURL:null,country:{name:"United Kingdom"}}},editorTwo:null,editorThree:null},{id:"11",title:"Cell Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/11.jpg",isOpenForSubmission:!0,annualVolume:11407,editor:{id:"133493",title:"Prof.",name:"Angel",middleName:null,surname:"Catala",slug:"angel-catala",fullName:"Angel Catala",profilePictureURL:"https://mts.intechopen.com/storage/users/133493/images/3091_n.jpg",biography:"Prof. Dr. Angel Catalá \r\nShort Biography Angel Catalá was born in Rodeo (San Juan, Argentina). He studied \r\nchemistry at the Universidad Nacional de La Plata, Argentina, where received aPh.D. degree in chemistry (Biological Branch) in 1965. From\r\n1964 to 1974, he worked as Assistant in Biochemistry at the School of MedicineUniversidad Nacional de La Plata, Argentina. From 1974 to 1976, he was a Fellowof the National Institutes of Health (NIH) at the University of Connecticut, Health Center, USA. From 1985 to 2004, he served as a Full Professor oBiochemistry at the Universidad Nacional de La Plata, Argentina. He is Member ofthe National Research Council (CONICET), Argentina, and Argentine Society foBiochemistry and Molecular Biology (SAIB). His laboratory has been interested for manyears in the lipid peroxidation of biological membranes from various tissues and different species. Professor Catalá has directed twelve doctoral theses, publishedover 100 papers in peer reviewed journals, several chapters in books andtwelve edited books. Angel Catalá received awards at the 40th InternationaConference Biochemistry of Lipids 1999: Dijon (France). W inner of the Bimbo PanAmerican Nutrition, Food Science and Technology Award 2006 and 2012, South AmericaHuman Nutrition, Professional Category. 2006 award in pharmacology, Bernardo\r\nHoussay, in recognition of his meritorious works of research. Angel Catalá belongto the Editorial Board of Journal of lipids, International Review of Biophysical ChemistryFrontiers in Membrane Physiology and Biophysics, World Journal oExperimental Medicine and Biochemistry Research International, W orld Journal oBiological Chemistry, Oxidative Medicine and Cellular Longevity, Diabetes and thePancreas, International Journal of Chronic Diseases & Therapy, International Journal oNutrition, Co-Editor of The Open Biology Journal.",institutionString:null,institution:{name:"National University of La Plata",institutionURL:null,country:{name:"Argentina"}}},editorTwo:null,editorThree:null},{id:"12",title:"Human Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/12.jpg",isOpenForSubmission:!0,annualVolume:11408,editor:{id:"195829",title:"Prof.",name:"Kunihiro",middleName:null,surname:"Sakuma",slug:"kunihiro-sakuma",fullName:"Kunihiro Sakuma",profilePictureURL:"https://mts.intechopen.com/storage/users/195829/images/system/195829.jpg",biography:"Professor Kunihiro Sakuma, Ph.D., currently works in the Institute for Liberal Arts at the Tokyo Institute of Technology. He is a physiologist working in the field of skeletal muscle. He was awarded his sports science diploma in 1995 by the University of Tsukuba and began his scientific work at the Department of Physiology, Aichi Human Service Center, focusing on the molecular mechanism of congenital muscular dystrophy and normal muscle regeneration. His interest later turned to the molecular mechanism and attenuating strategy of sarcopenia (age-related muscle atrophy). His opinion is to attenuate sarcopenia by improving autophagic defects using nutrient- and pharmaceutical-based treatments.",institutionString:null,institution:{name:"Tokyo Institute of Technology",institutionURL:null,country:{name:"Japan"}}},editorTwo:null,editorThree:{id:"331519",title:"Dr.",name:"Kotomi",middleName:null,surname:"Sakai",slug:"kotomi-sakai",fullName:"Kotomi Sakai",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000031QtFXQA0/Profile_Picture_1637053227318",biography:"Senior researcher Kotomi Sakai, Ph.D., MPH, works at the Research Organization of Science and Technology in Ritsumeikan University. She is a researcher in the geriatric rehabilitation and public health field. She received Ph.D. from Nihon University and MPH from St.Luke’s International University. Her main research interest is sarcopenia in older adults, especially its association with nutritional status. Additionally, to understand how to maintain and improve physical function in older adults, to conduct studies about the mechanism of sarcopenia and determine when possible interventions are needed.",institutionString:null,institution:{name:"Ritsumeikan University",institutionURL:null,country:{name:"Japan"}}}},{id:"13",title:"Plant Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/13.jpg",isOpenForSubmission:!0,annualVolume:11409,editor:{id:"332229",title:"Prof.",name:"Jen-Tsung",middleName:null,surname:"Chen",slug:"jen-tsung-chen",fullName:"Jen-Tsung Chen",profilePictureURL:"https://mts.intechopen.com/storage/users/332229/images/system/332229.png",biography:"Dr. Jen-Tsung Chen is currently a professor at the National University of Kaohsiung, Taiwan. He teaches cell biology, genomics, proteomics, medicinal plant biotechnology, and plant tissue culture. Dr. Chen\\'s research interests include bioactive compounds, chromatography techniques, in vitro culture, medicinal plants, phytochemicals, and plant biotechnology. He has published more than ninety scientific papers and serves as an editorial board member for Plant Methods, Biomolecules, and International Journal of Molecular Sciences.",institutionString:"National University of Kaohsiung",institution:{name:"National University of Kaohsiung",institutionURL:null,country:{name:"Taiwan"}}},editorTwo:null,editorThree:null}]},overviewPageOFChapters:{paginationCount:17,paginationItems:[{id:"81751",title:"NanoBioSensors: From Electrochemical Sensors Improvement to Theranostic Applications",doi:"10.5772/intechopen.102552",signatures:"Anielle C.A. Silva, Eliete A. Alvin, Lais S. de Jesus, Caio C.L. de França, Marílya P.G. da Silva, Samaysa L. Lins, Diógenes Meneses, Marcela R. Lemes, Rhanoica O. Guerra, Marcos V. da Silva, Carlo J.F. de Oliveira, Virmondes Rodrigues Junior, Renata M. 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