Carbonate matrix acidizing function

Surfactant-gelled acid systems (also known as viscoelastic acid systems) represent a more recent development. Such systems have found success in carbonate matrix acidizing applications in particular. Certain special surfactant formulations can be added to acid that is above a certain concentration (e.g., >15% HCl) at which the surfactant does not impart appreciable viscosity. However, as the acid is injected and reacts in the formation, the surfactant generates viscosity (as a function of dissolved chloride ion and pH), thereby retarding reaction and providing, potentially, in situ diversion. As acid spends further, viscosity breaks back to reduced level (in the ideal case). 

Phosphorus The main role of phosphorus in carbon materials is as an oxidation protector and a fire retardant [136-144]. Its source can be in phosphoric acid, which is used in some technologies of carbon activation [143,144] or in the cross-linking precursor. The phosphorus present in the carbon matrix is stable between 773 and 1273 K. It can be fixed as red phosphorus and/or in chemically bonded forms, such as -C-P-bonds or -C-O-P-bonds [143-145]. During the carbonization process at low temperatures, phosphocarbonaceous species are created. Their content decreases by scission of the P-O-C bonds with an increase in the temperature, due to the growth of aromatic structures [143]. Possible phosphorus-containing functionalities are presented in Figure 2.4. 

Composites made with carbon nanostructures have demonstrated their high performance as biomaterials, basically applied in the field of tissue regeneration with excellent results. For example, P.R. Supronowicz et al. demonstrated that nanocomposites fabricated with polylactic acid and CNTs can be used to expose cells to electrical stimulation, thus promoting osteoblast functions that are responsible for the chemical composition of the organic and inorganic phases of bone [277]. MacDonald et al. prepared composites containing a collagen matrix CNTs and found that CNTs do not affect the cell viability or cell proliferation [278]. 

In a sediment system, the hydrolysis rate constant of an organic contaminant is affected by its retention and release with the sohd phase. Wolfe (1989) proposed the hydrolysis mechanism shown in Fig. 13.4, where P is the organic compound, S is the sediment, P S is the compound in the sorbed phase, k and k" are the sorption and desorption rate constants, respectively, and k and k are the hydrolysis rate constants. In this proposed model, sorption of the compound to the sediment organic carbon is by a hydrophobic mechanism, described by a partition coefficient. The organic matrix can be a reactive or nonreactive sink, as a function of the hydrolytic process. Laboratory studies of kinetics (e.g., Macalady and Wolfe 1983, 1985 Burkhard and Guth 1981), using different organic compounds, show that hydrolysis is retarded in the sohd-associated phase, while alkaline and neutral hydrolysis is unaffected and acid hydrolysis is accelerated. 

The tricarboxylic acid cycle (TCA cycle, also known as the citric acid cycle or Krebs cycle) is a cyclic metabolic pathway in the mitochondrial matrix (see p. 210). in eight steps, it oxidizes acetyl residues (CH3-CO-) to carbon dioxide (CO2). The reducing equivalents obtained in this process are transferred to NAD"" or ubiquinone, and from there to the respiratory chain (see p. 140). Additional metabolic functions of the cycle are discussed on p. 138. 

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