Composition for dust suppression and containment of radioactive products of combustion

Abstract

The invention relates to means for protecting the environment from the consequences of fires complicated by a radiation factor. A composition for dust suppression and containment of radioactive products of combustion after a fire with a radiation factor has been extinguished comprises, as a surfactant, a mixture of an anionic, a non-ionic and an amphoteric surfactant, and has the following ratio of components: 3.0-7.0% by weight of an aqueous solution of polyvinyl alcohol (in terms of a mass fraction of dry product); 0.1-0.3% by weight of plasticizer; 11.0-29.0% by weight of surfactant; with water making up the remainder. The invention makes it possible to carry out dust suppression and containment of radioactive products of combustion which are formed on surfaces, including at elevated temperatures, after a fire has been extinguished.

Claims

1. A composition for dust suppression and containment of radioactive products of combustion after the extinguishing of a fire with a radiation factor, comprising÷ an aqueous solution of polyvinyl alcohol, a glycerine and a surfactant, wherein it contains a mixture of an anionic, a non-ionic and an amphoteric surfactant as a surfactant with the following proportions of components, wt %: TABLE-US-00005 an aqueous solution of polyvinyl alcohol (in terms of a 3.0-7.0 mass fraction of dry product) a glycerine 0.1-0.3 a surfactant 11.0-29.0 Water a remainder wherein the anionic surfactant is alkylbenzene sulfonate, the non-ionic surfactant is cocamidopropyl dimethylamine oxide, and the amphoteric surfactant is cocamidopropyl betaine.

2. The composition of claim 1, wherein an anionic surfactant alkylbenzene sulfonate is mixed with other substances in the amount of 1.0-3.0 wt %.

3. The composition of claim 1, wherein a non-ionic surfactant cocamidopropyl dimethylamine is mixed with other substances in the amount of 8.0-22.0 wt %.

4. The composition of claim 1, wherein an amphoteric surfactant cocamidopropyl betaine is mixed with other substances in the amount of 2.0-4.0 wt %.

Description

EMBODIMENT

(1) An example of preparation of the composition.

(2) The composition is produced by dissolving polymer film-forming polyvinyl alcohol in water (for example, in an electrical boiling pot of KPE-60 trade mark) for 30 minutes at 60-80° C. After cooling, glycerine, sulfonol P, OXI SAA AP.30, and BETA SAA AP.45 are loaded sequentially while the composition is stirred. Stirring continues for 5 minutes after each component is loaded.

(3) The results of tests are given in Table 2.

(4) The composition viscosity was determined in accordance with GOST 9070-75.

(5) The period over which the coating maintains its protective properties was determined according to the procedure MI IRRT-04-2014 of Saint Petersburg State Institute of Technology (Technical University) SPbSIT (TU), developed in accordance with GOST R 51037-97, GOST R 50773-95, GOST 4.54-79, and GOST R 19465-74. The samples contaminated by radionuclides were measured by using the UMF 2000 radiometric unit for recording α- and β-radiation. The composition was applied to the samples contaminated by radiation. After drying, the level of radioactive contamination of the external surface of the coating under test was determined by swabbing at time intervals of 24 hours; 15, 30, 60, 120, and 180 days.

(6) The appearance of the coating on smoldering embers with ash was determined visually on the basis of the presence or absence of a continuous coating.

(7) The diameters of bubbles and their lifespan were determined according to the equipment integrity control method with a sensitivity range of the means of leak detection of 1.Math.10.sup.−5 to 1.Math.10.sup.−7 m.sup.3Pa/s on a diffuse reference leak sample SOP DKT-1 with a gas flow rate of 3 mm.sup.3/s, 4 atm.

(8) The time foam breakdown began and ended was determined visually by observing and recording the time of these events.

(9) The foam expansion ratio was determined as the ratio of the foam volume to the composition solution volume, obtained after foam syneresis.

(10) The degree of lump formation was determined according to the procedure MI IRRT-05-2014 of SPbSIT (TU), developed in accordance with GOST R 51037-97, GOST 4.54-79, and GOST R 19465-74. The lump formation level was determined from the following measurements: measurement of the mass fraction of the model dust fraction with a diameter of particles exceeding the critical value after application of the composition on a dust-forming surface. A maximum particle size of 100 μm was taken as the critical value. The mass fraction of the model dust fraction was expressed as a percentage of the total amount of model dust. After application of the composition on a dust-forming surface, the mass of the lump fraction and then the proportion of the lump fraction compared to the initial dry mass were calculated.

(11) Analysis of Results

(12) As Tables 1 and 2, Examples 1-3, show, when the mass fraction of the dry product of the film-forming polyvinyl alcohol is within the range of 3.0-7.0%, the composition covers the embers uniformly and permeates the top layer of the ash, forming a continuous coating. In terms of its scope of use, the coating meets the requirements of GOST R 51037-97—it continues to provide protection for more than 180 days.

(13) When the content of glycerine plasticizer is within the range of 0.1-0.3%, the composition possesses stable foam-forming properties at high values of bubble lifespan, foam expansion ratio and lump formation level.

(14) When the content of SAA sulfonol P is within the range of 1.0-3.0%, the drying composition forms a continuous coating, and it continues to provide protection for the required length of time.

(15) When the content of SAA OXI SAA AP.30 is within the range of 8.0-22.0%, the applied composition does not “sink” into the ash layer, and it possesses stable foam-forming properties and forms a continuous coating.

(16) When the content of SAA BETA SAA AP.45 is within the range of 2.0-4.0%, the composition has stable wetting properties, covers embers uniformly and permeates the top layer of ash.

(17) Examples of use of the compositions with a quantitative composition different from that claimed in the Claims (No. 4-13).

(18) When the weight fraction of the dry product of the film-forming polyvinyl alcohol is less than 3%, a coating is not formed.

(19) When the weight fraction of the dry product of the film-forming polyvinyl alcohol is more than 7%, the foam-forming process is slowed down due to the increased viscosity of the solution, and the coating formed provides protection for an unsatisfactory length of time.

(20) When the content of the glycerine plasticizer is less than 0.1%, the bubble lifespan decreases, which results in fewer ash particles being drawn into the foam and a reduction of the time period, for which the coating provides protection.

(21) When the content of the glycerine plasticizer is more than 0.3%, the foam-forming rate decreases, and the products of combustion permeate in an uneven manner, which results in reduction of the time period, for which the coating provides protection.

(22) When the content of SAA sulfonol P is less than 0.2%, the time period, for which the coating formed by the composition provides protection, is reduced.

(23) When the content of SAA sulfonol P is more than 3.0%, the size of the bubbles increases, which results in voids inside the drying coating, i.e. in a discontinuous coating and a sharp decrease in the time period, for which the coating provides protection.

(24) When the content of SAA OXI SAA AP.30 is less than 8.0%, the time period, for which the coating formed provides protection, is unsatisfactory.

(25) When the content of SAA OXI SAA AP.30 is more than 22.0%, the foam-forming process continues at the same level; there is therefore no reason to consume more material for the reasons of economy.

(26) When the content of SAA BETA SAA AP.45 is less than 2.0%, the time period, for which the coating formed by the composition provides protection, is reduced.

(27) When the content of SAA BETA SAA AP.45 is more than 4.0%, the foam retains the same wetting properties; there is therefore no reason to consume more material for the reasons of economy.

(28) When applied on products of combustion, the prototype composition (Example No. 14) “sinks” into the top layer of ash, failing to uniformly wet the surface and form a uniform coating.

(29) The test results confirm that the proposed composition is designed to meet the objective set and that it complies with all the criteria for registration according to the applicable legislation.

(30) TABLE-US-00003 TABLE 1 Qualitative and quantitative (wt %) makeup of the proposed composition Example No. 14 List of components 1 2 3 4 5 6 7 8 9 10 11 12 13 prototype Polyvinyl alcohol 3.0 5.0 7.0 2.0 8.0 6.0 4.0 5.0 7.0 3.0 4.0 (6.0 5.0  7.0 Glycerine 0.1 0.2 0.3 0.1 0.3 0.05 0.4 0.3 0.1 0.2 0.2 0.3 0.1 — Sulfonol P 1.0 2.0 3.0 3.0 2.0 3.0 1.0 0.5 4.0 1.0 3.0 2.0 3.0 OP-71.0 OXI SAA AP.30 8.0 15.0 22.0 10.0 12.0 9.0 10.0 10.0 18.0 7.0 23.0 46.0 15.0 — BETA SAA AP.45 2.0 3.0 4.0 2.0 3.0 4.0 2.0 3.0 4.0 2.0 4.0 1.0 5.0 — water 85.9 74.8 63.7 82.7 74.9 77.95 82.6 81.2 66.9 86.8 65.8 74.7 71.9 92.0

(31) TABLE-US-00004 TABLE 2 Dust suppression and containment properties of the proposed composition Properties of coatings Characteristics of properties as per Examples No, 1-14 Example No. 1 2 3 4 5 6 7 Composition viscosity, s 18 17 18 12 30 19 18 Duration of protective >180 >180 >180 0 15 60 30 properties, days Contaminating .sup.50Co >180 >180 >180 0 15 60 30 radionuclide: .sup.90Sr—.sup.90Y >180 >180 >180 0 60 120 60 .sup.137Cs >180 >180 >180 0 15 60 60 .sup.255Pu Appearance of coating Continuous Continuous Continuous Coating is Continuous Continuous Continuous on smoldering embers coating coating coating not formed coating coating coating with ash Bubble diameter, mm 30 28 32 20 12 20 15 Bubble lifespan, min 50 55 51 10 25 12 30 Time of beginning of 60 50 56 5 15 20 25 breakdown of foam, min Time of end of 110 100 110 15 60 60 50 breakdown of foam, min Foam volume, mL 1,000 1,000 1,000 1,000 1,000 1,000 1,000 Liquid volume, mL 20 18.7 19.2 50 200 50 25 Foam expansion ratio 50 54 52 20 5 20 40 Degree of lump 82.6 84.4 82.8 0.0 38.8 45.5 39.1 formation, % Properties of coatings Characteristics of properties as per Examples No, 1-14 Example No. 14 8 9 10 11 12 13 Prototype Composition 18 18 17 17 18 17 35 viscosity, s Duration of protective 120 <15 15 60 30 60 0 properties, days Contaminating .sup.50Co 60 <15 30 120 60 120 0 radionuclide: .sup.90Sr−.sup.90Y 120 <15 30 120 60 120 0 .sup.137Cs 60 <15 10 120 30 60 0 .sup.255Pu Appearance of coating Continuous Discontinuity Continuous Continuous Continuous Continuous Coating is on smoldering embers coating of coating coating coating coating coating not formed with ash Bubble diameter, mm 10 35 20 30 20 28 5 Bubble lifespan, min 50 30 40 55 40 55 20 Time of beginning of 50 50 45 60 45 50 15 breakdown of foam, min Time of end of 110 120 90 110 90 100 2.5 breakdown of foam, min Foam volume, mL 1,000 1,000 1,000 1,000 1,000 1,000 1,000 Liquid volume, mL 25 20 25 20 25 20 25 Foam expansion ratio 40 50 40 50 40 50 40 Degree of lump 51.2 18.8 42.2 61.1 48.8 62.2 0.0 formation, %