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Batch assay

Different effects of formaldehyde on the hydrolysis of urea are reported. On the one hand, Garrido and colleagues,3 applying anoxic conditions, observed that an inhibitory effect started at 50 mg/L formaldehyde and the levels of inhibition were 50% and 90% for concentrations of formaldehyde of 100 mg/L and 300 mg/L, respectively. Similar effects were found by Campos and colleagues,33 working with an anoxic USB, who observed that formaldehyde concentrations in the reactor of 250 to 300 mg/L caused an inhibition of around 53%. This inhibition on the ureolytic activity was also reported by Walker.36 On the other hand, Eiroa and colleagues37 carried out batch assays at different initial urea concentrations from 90 to 370mg/L N-urea in the presence of 430 mg/L formaldehyde. They observed that a complete hydrolysis was achieved and initial urea hydrolysis rates remained constant. [Pg.769]

Figure 1 Schematic diagram of a fiberoptic sensor for batch assay. PMT, photomultiplier tube HV, high-voltage supplier. Figure 1 Schematic diagram of a fiberoptic sensor for batch assay. PMT, photomultiplier tube HV, high-voltage supplier.
Shabana, E.F. 1987. Use of batch assays to assess the toxicity of atrazine to some selected cyanobacteria. 1. Influence of atrazine on the growth, pigmentation and carbohydrate contents of Aulosira fertilissima, Anabaena oryzae, Nostoc muscorum and Tolypothrix tenuis. Jour. Basic Microbiol. 2 113-119. [Pg.802]

TABLE 14 Single-Batch Assay Results (%LC) for Example 1... [Pg.602]

The infrared spectrum given in Figure 1 was determined for a KBr pellet preparation of silver sulfadiazine with the use of a Beckman IR 10 spectrometer. The assignments for important absorption bands are presented — as far as possible — in Table I. The assignments are based on various literature references (4, 8,9). In practice it is found that different batches of silver sulfadiazine do produce slightly different IR spectra, while the batches assay closely to the theoretical values (4,5,9). [Pg.555]

The main variable of design for a CSTR is the hydraulic retention time (HRT), which represents the ratio between volume and flow rate, and it is a measure of the average length of time that a soluble compound remains in the reactor. Capital costs are related to HRT, as this variable directly influences reactor volume [83]. HRT can be calculated by means of a mass balance of the system in that case, kinetic parameters are required. Some authors obtained kinetic models from batch assays operating at the same reaction conditions, and applied them to obtain the HRT in continuous operation [10, 83, 84]. When no kinetic parameters are available, HRT can be estimated from the time required to complete the reaction in a discontinuous process. One must take into account that the reaction rate in a continuous operation is slower than in batch systems, due to the low substrate concentration in the reactor. Therefore, HRT is usually longer than the total time needed in batch operation [76]. [Pg.257]

Although some efforts are being made to develop EMRs based on the immobilization of peroxidases onto the membrane [106, 112], the most applied configurations correspond to the use of direct contact reactors for wastewater treatment, with SBP and MnP applied to effluents containing both phenols [74] and dyes [8, 85]. Some attempts were made to apply an EMR for the synthesis of oxindole from indole by CPO [86]. However, the reactor was only stable for a short period (10 residence times). Afterward, the polymerization of oxindole yielded a solid substance, which blocked the membrane, causing enzyme deactivation and the reduction of the total turnover numbers compared to those obtained in batch assays. [Pg.261]

Fig. 10.2. Sensing principles for the determination of the biochemical oxygen demsind (BOD), (a) Immobilized cells on the surface of a Clark electrode and (b) batch assay with cells in suspension and with a redox mediator. Fig. 10.2. Sensing principles for the determination of the biochemical oxygen demsind (BOD), (a) Immobilized cells on the surface of a Clark electrode and (b) batch assay with cells in suspension and with a redox mediator.
The absorbance is useful as a measure of purity from extraneous materials and can serve as a formulation batching assay. It can be used for chromatographic detection and quantitation-. ... [Pg.386]

Kanter, P.-M. and Schwarz, H.S. (1978) Hydroxylapatite batch assay for quantitation of cellular... [Pg.253]

Flow injection analysis (FIA) is based on the injection of a defined volume of liquid sample into a moving stream of a suitable liquid. It was developed to overcome the disadvantages of batch assay and continuous-flow analysis forms of chemical analysis and as a means of automating wet chemical reactions. In batch assays, the sample is mixed... [Pg.229]

Remove 100 pL aliquots from the supernatant (avoid the oil ) for transmitter analysis. (Aliquots may be subdivided permitting measurements of multiple transmitters from a single sample). Treat the samples in the manner appropnate for the type of transmitter ultimately to be measured For amino acids, add TCA to 10% (v/v) for neuropeptides or catecholamines, add 3 vol of methanol 10 Store the samples at-20 C until further analysis (see Note 21). Measurements of diverse transmitters released from hippocampal synaptosomes in a typical release batch assay are shown in Fig. 3. [Pg.41]

Prepare stock solutions of depolarizing agents so that adding of 3 pL of the stock solution to a release batch assay tube (containing 125-150 pL) achieves the desired final concentration of depolarizing agent (i e., 40-50X stocks)... [Pg.44]

Angelidaki, L, Alves, M., Bolzonella, D., Borzacconi, L., Campos, J.L., Guwy, A.J., Kalyuzhnyi, S., Jenicek, P. van Lier, IB. 2009. Defining the biomethane potential (BMP) of solid organic wastes and energy crops a proposed protocol for batch assays. Water Set Technol. 59(5) 927-934. [Pg.28]

Chamchoi, N., Garcia, H., Angelidaki, I., 2011. Methane potential of household waste batch assays determination. Journal of Environmental Resource 33, 13—26. [Pg.293]


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See also in sourсe #XX -- [ Pg.229 ]




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Release batch assay

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