Phosphorous measurements

Figure 5. TG curves for polyurethanes (PU s) (containing 20 wt% of lignin) prepared with polyol containing phosphorous measured in air. Number indicated for each line shows the content of polyol with phosphorous expressed in wt%. Heating rate 10°C/min. Flow rate 15 ml/min.

Alaruri, S. McFarland, D. Brewington, A. Thomas, M. Sallee, N. Development of a fiber-optic probe for thermographic phosphor measurements in turbine engines. Opt. Lasers Eng. 1995, 22, 17. 

Table 9. Characteristics of the UV method for total phosphorous measurement (without dilution)...

It was found that that in the case of soft beta and X-ray radiation the IPs behave as an ideal gas counter with the 100% absorption efficiency if they are exposed in the middle of exposure range ( 10 to 10 photons/ pixel area) and that the relative uncertainty in measured intensity is determined primarily by the quantum fluctuations of the incident radiation (1). The thermal neutron absorption efficiency of the present available Gd doped IP-Neutron Detectors (IP-NDs) was found to be 53% and 69%, depending on the thicknes of the doped phosphor layer ( 85pm and 135 pm respectively). No substantial deviation in the IP response with the spatial variation over the surface of the IP was found, when irradiated by the homogeneous field of X-rays or neutrons and deviations were dominated by the incident radiation statistics (1). 

The total phosphoms content of the sample is determined by method AOCS Ja 5-55. Analysis of phosphoUpid in lecithin concentrates (AOCS Ja 7-86) is performed by fractionation with two-dimensional thin-layer chromatography (tic) followed by acid digestion and reaction with molybdate to measure total phosphorous for each fraction at 310 nm. It is a semiquantitative method for PC, PE, PI, PA, LPC, and LPE. Method AOCS Ja 7b-91 is for the direct deterrnination of single phosphoHpids PE, PA, PI, PC in lecithin by high performance Hquid chromatography (hplc). The method is appHcable to oil-containing lecithins, deoiled lecithins, lecithin fractions, but not appHcable to lyso-PC and lyso-PE. 

Phosphoric acid, aside from its acidic behavior, is relatively unreactive at room temperature. It is sometimes substituted for sulfuric acid because of its lack of oxidising properties (see SuLFURic ACID AND SULFURTRIOXIDe). The reduction of phosphoric acid by strong reducing agents, eg, H2 or C, does not occur to any measurable degree below 350—400°C. At higher temperatures, the acid reacts with most metals and their oxides. Phosphoric acid is stronger than acetic, oxaUc, siUcic, and boric acids, but weaker than sulfuric, nitric, hydrochloric, and chromic acids. 

A method suitable for analysis of sulfur dioxide in ambient air and sensitive to 0.003—5 ppm involves aspirating a measured air sample through a solution of potassium or sodium tetrachloromercurate, with the resultant formation of a dichlorosulfitomercurate. Ethylenediaminetetraacetic acid (EDTA) disodium salt is added to this solution to complex heavy metals which can interfere by oxidation of the sulfur dioxide. The sample is also treated with 0.6 wt % sulfamic acid to destroy any nitrite anions. Then the sample is treated with formaldehyde and specially purified acid-bleached rosaniline containing phosphoric acid to control pH. This reacts with the dichlorosulfitomercurate to form an intensely colored rosaniline—methanesulfonic acid. The pH of the solution is adjusted to 1.6 0.1 with phosphoric acid, and the absorbance is read spectrophotometricaHy at 548 nm (273). 

We have also looked at the lap shear strength of selected EB-ciirable epoxy adhesives. Because the adhesives being developed were being used for both aluminum-to-aluminum and composite-to-composite applications the lap shear strengths for both adherends was measured. Aluminum adherends were T2024 phosphoric acid anodized according to ASTM 3933. The composite adherends... 

The coil (wound on a light metal former) can be suspended by a fine strip of phosphor bronze between the pole pieces. Attached to this suspension is a small mirror which reflects on to a scale a beam of light which is focused upon it. An instrument of this kind is known as a D Arsonval galvanometer and is used in potentiometer circuits and various methods of measurement of resistance. 

Tests for quality of sealing of anodic coatings have become internationally standardised. They include dye spot tests with prior acid treatment of the surface (ISO 2143 1981 and BS 6161 Part 5 1982), measurement of admittance or impedance (ISO 2931 1983 and BS 6161 Part 6 1984), or measurement of weight loss after acid immersion (ISO 3210 1983 and BS 6161 Part 3 1984, and ISO 2932 1981 and BS 6161 Part 4 1981). Of these the chromic-phosphoric acid immersion test (ISO 3210) has become the generally accepted reference test. 

Pipette a 25 mL or 50 mL aliquot of the clear sample solution into a 250 mL conical flask, add 5 mL concentrated sulphuric acid, 5 mL 85 per cent phosphoric(V) acid, and 1-2 mL of 0.1 M silver nitrate solution, and dilute to about 80 mL. Add 5 g potassium persulphate, swirl the contents of the flask until most of the salt has dissolved, and heat to boiling. Keep at the boiling point for 5-7 minutes. Cool slightly, and add 0.5 g pure potassium periodate. Again heat to boiling and maintain at the boiling point for about 5 minutes. Cool, transfer to a lOOmL graduated flask, and measure the absorbances at 440 nm and 545 nm in 1 cm cells. 

In the phosphor-photoelectric detector used as just described, the x-ray quanta strike the phosphor at a rate so great that the quanta of visible light are never resolved they are integrated into a beam of visible light the intensity of which is measured by the multiplier phototube. In the scintillation counters usual in analytical chemistry, on the other hand, individual x-ray quanta can be absorbed by a single crystal highly transparent to light (for example, an alkali halide crystal with thallium as activator), and the resultant visible scintillations can produce an output pulse of electrons from the multiplier phototube. The pulses can be counted as were the pulses-from the proportional counter. 

Glaser and Lichtenstein (G3) measured the liquid residence-time distribution for cocurrent downward flow of gas and liquid in columns of -in., 2-in., and 1-ft diameter packed with porous or nonporous -pg-in. or -in. cylindrical packings. The fluid media were an aqueous calcium chloride solution and air in one series of experiments and kerosene and hydrogen in another. Pulses of radioactive tracer (carbon-12, phosphorous-32, or rubi-dium-86) were injected outside the column, and the effluent concentration measured by Geiger counter. Axial dispersion was characterized by variability (defined as the standard deviation of residence time divided by the average residence time), and corrections for end effects were included in the analysis. The experiments indicate no effect of bed diameter upon variability. For a packed bed of porous particles, variability was found to consist of three components (1) Variability due to bulk flow through the bed... 

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