CN106683731B - Spent Radioactive liquid processing method, Spent Radioactive liquid processing device and equipment - Google Patents

Spent Radioactive liquid processing method, Spent Radioactive liquid processing device and equipment Download PDF

Info

Publication number
CN106683731B
CN106683731B CN201611207471.5A CN201611207471A CN106683731B CN 106683731 B CN106683731 B CN 106683731B CN 201611207471 A CN201611207471 A CN 201611207471A CN 106683731 B CN106683731 B CN 106683731B
Authority
CN
China
Prior art keywords
reactor
adsorbent
supernatant
radioactive liquid
waste
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201611207471.5A
Other languages
Chinese (zh)
Other versions
CN106683731A (en
Inventor
戴忠华
黄卫刚
赵滢
方军
赵璇
李福志
尉继英
张猛
洪振旻
王勤湖
于兴毫
司鹏昆
林尧炳
陈跃
夏子世
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
China General Nuclear Power Corp
CGN Power Co Ltd
Lingdong Nuclear Power Co Ltd
Original Assignee
China General Nuclear Power Corp
CGN Power Co Ltd
Lingdong Nuclear Power Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by China General Nuclear Power Corp, CGN Power Co Ltd, Lingdong Nuclear Power Co Ltd filed Critical China General Nuclear Power Corp
Priority to CN201611207471.5A priority Critical patent/CN106683731B/en
Publication of CN106683731A publication Critical patent/CN106683731A/en
Application granted granted Critical
Publication of CN106683731B publication Critical patent/CN106683731B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21FPROTECTION AGAINST X-RADIATION, GAMMA RADIATION, CORPUSCULAR RADIATION OR PARTICLE BOMBARDMENT; TREATING RADIOACTIVELY CONTAMINATED MATERIAL; DECONTAMINATION ARRANGEMENTS THEREFOR
    • G21F9/00Treating radioactively contaminated material; Decontamination arrangements therefor
    • G21F9/04Treating liquids
    • G21F9/06Processing
    • G21F9/12Processing by absorption; by adsorption; by ion-exchange

Abstract

The invention discloses a kind of Spent Radioactive liquid processing method, Spent Radioactive liquid processing device and equipment.Radioactive liquid waste is handled by the liquid waste treating apparatus including first reactor and second reactor two-stage cascade, radionuclide amount is few in the second obtained supernatant, meets discharge standard.Energy consumption is small, treating capacity is big, and the radioactive solid waste amount of generation is less.

Description

Spent Radioactive liquid processing method, Spent Radioactive liquid processing device and equipment
Technical field
The present invention relates to liquid waste disposal technique field, more particularly, to a kind of Spent Radioactive liquid processing method, Spent Radioactive Liquid processing device and equipment.
Background technology
Substantial amounts of middle low-activity waste liquid can be produced in nuclear power station operational process, the waste liquid containing radionuclide is for example direct Discharge, will produce serious harm to health and natural environment.Therefore discharge mark is reached after must handling it Standard could discharge.Be traditionally used for concentrating or separate the method for radionuclide in radioactive liquid waste mainly have evaporation, filtering, from Son exchanges or is the combination of these technologies.By taking Daya Bay nuclear power plant as an example, process waste liquor uses " filtering+ion exchange+steaming Hair " process, chemical waste fluid use " filtering+evaporation " process, and ground waste liquid uses " filtering+evaporation " process.
However, it is high energy consumption technique to be concentrated by evaporation, 1m is handled using evaporation concentration method3Low radioactive waste liquid, only energy consumption cost will Reach thousands of members, do not meet with the energy saving and environmental-friendly sustainable energy development strategy for characteristic.A such as only TEU evaporation Device for avoid the crystallization of concentrate boron need 24 it is small when keep stand-by heat recurrent state, and need in evaporation process input substantial amounts of SVA auxiliary steams.Since TEU evaporations and TEP evaporators need to keep stand-by heat circular flow, its forced circulation pump for a long time The failure-frequency of TEU006PO and TEP008/009PO is higher with respect to other pumps.And due to long-play, TEU/TEP evaporations The radioactive dosage of device and its auxiliary device significantly raises, and needs strictly to control dosage and implement dosage and share in maintenance process, Therefore corresponding maintenance cost and human cost are higher.In addition evaporator will produce a collection of 4m every year on average3The high radiation of left and right Property concentrate, solid waste yield reaches 16 cubic metres or so after cement solidification, and the processing cost of solid waste is very high.Additionally due to need With pipeline decontamination, complexing agent is often introduced into surfactant into chemical waste fluid, on evaporation process complexing agent and surface Activating agent will cause concentrate largely to foam so as to influence the quality of distillate, due to being unable to control generation and the receipts of upstream waste liquid Collection, TEU evaporator effectiveness are often influenced by concentrate foaming, influence treatment effect.
In addition, during by ion-exchange process Adsorption of Radioactive nucleic, the general pattern for using fixed bed reactors, radiation Property waste liquid by be loaded with ion exchange resin fixed bed reactors occur ion exchange.But since ion exchange resin does not have Selectivity, in the high waste liquid of salt content, resin is soon because conventional ion is failed by exchange saturation at the same time.Using Daya Gulf as Example, for TEU except the mixed bed that salt bed configuration is two series connection, series is less, lacks preprocessing function, and do not possess selective desalination work( Can, integrated treatment efficiency is low, and the clarification time is partially long.When TEU evaporators are unavailable, it is necessary to which the waste liquid of evaporation process can only pass through Fluid reservoir is kept in, although removing salt bed purified treatment temporarily by one, due to this temporarily except salt bed capacity it is smaller and long when Between operation be easy to cause radioactive dosage and raise rapidly, liquid waste processing is relatively difficult, it is necessary to set more storage tank to be put to store Penetrating property waste liquid.Further, since containing more with nucleic existing for colloidal attitude in nuclear power station radioactive liquid waste, such as110mAg、58Co、60Co etc., be easy to be attached to causes to make ion exchange resin saturation on resin, evaporates and the treatment effect of ion exchange is all bad, The cycle time of ion exchange resin, replace it is frequent, radioactive spent resin yield it is higher, it is necessary to stabilized and curing at Reason, radioactive solid waste amount is more, and processing, disposal costs are sufficiently expensive, add the totle drilling cost of Radioactive waste management, this is Nuclear power station urgent problem to be solved at present.
To sum up, the radioactive solid waste amount that traditional Spent Radioactive liquid processing method energy consumption is big, produces is more.
The content of the invention
Based on this, it is necessary to provide at the radioactive liquid waste that a kind of energy consumption is small, the radioactive solid waste amount of generation is less Reason method and treating apparatus for radioactive waste liquid.
A kind of Spent Radioactive liquid processing device, including:
First reactor, is equipped with the first blender in the first reactor, the first reactor equipped with first into Liquid mouth and the first liquid outlet, first inlet are used to flow into radioactive liquid waste in the first reactor, during use Load the first adsorbent in the first reactor, first blender be used to stirring and evenly mixing the radioactive liquid waste with it is described First adsorbent;And
Second reactor, is equipped with the second blender in the second reactor, the second reactor equipped with second into Liquid mouth and the second liquid outlet, second inlet are connected with first liquid outlet by pipeline, and second inlet is used The first supernatant for being formed is flowed into the second reactor after by first reactor processing, described second during use Load the second adsorbent in reactor, second blender is used to stir and evenly mix first supernatant and the described second absorption Agent, second liquid outlet are used for the second supernatant discharge second reaction that will be formed after second reactor processing Device.
A kind for the treatment of apparatus for radioactive waste liquid, including at least the above Spent Radioactive liquid processing device, the Spent Radioactive It is in be connected in parallel between liquid processing device.
A kind of Spent Radioactive liquid processing method, includes the following steps:
Above-mentioned Spent Radioactive liquid processing device or above-mentioned treating apparatus for radioactive waste liquid are provided;
Radioactive liquid waste is flowed into the first reactor, by first blender by the radioactive liquid waste with First adsorbent stirs and evenly mixs, and first adsorbent adsorbs the radionuclide in the radioactive liquid waste;
The first supernatant and the first precipitation are obtained after standing sedimentation;
First supernatant is flowed into the second reactor, by second blender by first supernatant Liquid is stirred and evenly mixed with second adsorbent, and second adsorbent adsorbs the radionuclide in first supernatant;
The second supernatant and the second precipitation are obtained after standing sedimentation;And
When second supernatant meets discharge standard, second supernatant is discharged into the second reactor.
In one embodiment, it is described to flow into radioactive liquid waste before the operation in the first reactor, also wrap The operation for collecting radioactive liquid waste is included, the radioactive liquid waste of collection is flowed into described first by way of in batches afterwards In reactor, after first supernatant flows into the operation in the second reactor, flowed into the first reactor Enter the radioactive liquid waste of next batch.
In one embodiment, the solid-to-liquid ratio of first adsorbent and the radioactive liquid waste is 20g/L~60g/ L, the solid-to-liquid ratio of second adsorbent and first supernatant is 20g/L~60g/L.
In one embodiment, the method, which is additionally included in, uses the Spent Radioactive liquid processing device or the radiation Property waste liquor treatment equipment for a period of time after, replace first adsorbent in the first reactor, and by described first Reactor and the liquid flow direction of the second reactor are exchanged, and described method includes following steps afterwards:
The radioactive liquid waste is flowed into the second reactor, by second blender by the Spent Radioactive Liquid is stirred and evenly mixed with second adsorbent, and second adsorbent adsorbs the radionuclide in the radioactive liquid waste;
The 3rd supernatant and the 3rd precipitation are obtained after standing sedimentation;
3rd supernatant is flowed into the first reactor, by first blender by the 3rd supernatant First adsorbent after liquid and replacement stirs and evenly mixs, and first adsorbent after replacement is by the 3rd supernatant Radionuclide absorption;
The 4th supernatant and the 4th precipitation are obtained after standing sedimentation;And
When the 4th supernatant meets discharge standard, the 4th supernatant is discharged into the first reactor.
In one embodiment, it is described to be inhaled the radioactive liquid waste and described first by first blender In the attached dose of operation stirred and evenly mixed, stir speed (S.S.) is 250rpm~350rpm, and mixing time is 2min~3min;Described stand is sunk In the operation that the first supernatant and the first precipitation are obtained after drop, the standing sedimentation time is 2min~3min.
In one embodiment, it is described to be adsorbed first supernatant and described second by second blender In the operation that agent stirs and evenly mixs, stir speed (S.S.) is 250rpm~350rpm, and mixing time is 2min~3min;The standing sedimentation In the operation for obtaining the second supernatant and the second precipitation afterwards, the standing sedimentation time is 2min~3min.
In one embodiment, first adsorbent includes inorganic adsorbing material and is coated on the inorganic adsorbent Magnetic core carrier Fe on material3O4;Second adsorbent includes inorganic adsorbing material and is coated on the inorganic adsorbing material On magnetic core carrier Fe3O4
In one embodiment, the particle diameter of first adsorbent is 10 μm~30 μm, the grain of second adsorbent Footpath is 10 μm~30 μm.
Above-mentioned Spent Radioactive liquid processing device is simple in structure, changes general use fixed bed reactors absorption mode, and It is radioactive liquid waste is mixed with adsorbent by stirring radioactive liquid waste, by first reactor and second reactor two-stage After adsorption treatment, radionuclide amount is few in the second obtained supernatant, meets discharge standard.Even existing for colloidal attitude Nucleic, can also be handled, less energy consumption by above-mentioned Spent Radioactive liquid processing device, and the radioactive solid waste amount of generation is less.
The processing method of above-mentioned radioactive liquid waste, passes through the radiation including first reactor and second reactor two-stage cascade Property liquid waste treating apparatus handle radioactive liquid waste, radioactive liquid waste flows into the first reactor equipped with the first adsorbent and carries out Adsorption reaction, makes the mixing of radioactive liquid waste and the first adsorbent after the stirring of the first blender, the first adsorbent is by radioactive liquid waste In radionuclide absorption.After standing sedimentation, most of radionuclide settles to form the first precipitation with the first adsorbent, and First supernatant, which is flowed into the second reactor equipped with the second adsorbent, carries out adsorption reaction, makes first after the stirring of the second blender Supernatant and the second adsorbent mix, and the second adsorbent adsorbs the radionuclide in the first supernatant.After standing sedimentation, put Penetrating property nucleic settles to form the second precipitation with the second adsorbent.Test result indicates that reacted by first reactor and second After device two-stage adsorption treatment, radionuclide amount is few in the second obtained supernatant, meets discharge standard.Even colloidal attitude Existing nucleic, can also be adsorbed by the first adsorbent or the second adsorbent and be precipitated during standing sedimentation, therefore radiate Property waste liquid can directly carry out two-stage adsorption treatment, can save the operation of evaporation process, energy consumption is small.First adsorbent and the second suction Attached dose can be repeated several times use, and treating capacity is big, and the radioactive solid waste amount of generation is less.
Brief description of the drawings
Fig. 1 is the structure diagram of the Spent Radioactive liquid processing device of an embodiment;
Fig. 2 is the flow diagram when handling radioactive liquid waste of Spent Radioactive liquid processing device as shown in Figure 1;
Fig. 3 is the structure diagram of the treating apparatus for radioactive waste liquid of an embodiment;
Fig. 4 is the flow chart of the Spent Radioactive liquid processing method of an embodiment;
Fig. 5 is that the dosage of adsorbent in embodiment 1 is respectively to Cs under the conditions of 20g/L, 40g/L, 60g/L+Go Except rate versus time curve figure;
Fig. 6 is the size distribution situation map that the adsorbent in embodiment 2 is measured using laser particle size analyzer;
Fig. 7 is the process schematic of sedimentation experiment in embodiment 2;
Fig. 8 is the decontamination factor of first reactor, the decontamination factor of second reactor and first reactor in embodiment 3 Decontamination factor with second reactor totality is with the curve map for handling batch variation;
Fig. 9 is the aqueous concentration of first reactor in embodiment 3 and the aqueous concentration of second reactor with processing batch The curve map of change;
Figure 10 is the Cs of single batch in first reactor and second reactor in embodiment 3+The song of the change of adsorbance Line chart;
The Cs added up in Figure 11 embodiments 3 in first reactor and second reactor+The curve map of adsorbance change;
Figure 12 is the decontamination factor of first reactor in embodiment 6, the decontamination factor of second reactor and the first reaction Device and the decontamination factor of second reactor totality with the change of processing batch curve map;
Figure 13 is first reactor and second reactor when adsorbent dosage is respectively 40g/L and 60g/L in embodiment 6 Overall decontamination factor with the change of processing batch curve map.
Embodiment
In order to make the foregoing objectives, features and advantages of the present invention clearer and more comprehensible, below in conjunction with the accompanying drawings to the present invention Embodiment be described in detail.Many details are elaborated in the following description in order to fully understand this hair It is bright.But the invention can be embodied in many other ways as described herein, those skilled in the art can be not Similar improvement is done in the case of running counter to intension of the present invention, therefore the present invention is not limited to the specific embodiments disclosed below.
Referring to Fig. 1, the Spent Radioactive liquid processing device 10 of an embodiment, including first reactor 100, second are reacted Device 200 and exhausted bath box 300.The first blender 110 is equipped with first reactor 100.Stirred in second reactor 200 equipped with second Mix device 210.First reactor 100 is connected with second reactor 200.
Specifically, first reactor 100 is equipped with the first inlet 101 and the first liquid outlet 103, the first inlet 101 For radioactive liquid waste to be flowed into first reactor 100, second reactor 200 goes out equipped with the second inlet 201 and second Liquid mouth 203, the first liquid outlet 103 are connected with the second inlet 201 by pipeline.Further, in the duct be equipped with switch, with And kinetic pump is to control the flow rate of liquid.Load the first adsorbent, second reactor during use in first reactor 100 Load the second adsorbent in 200.
Exhausted bath box 300 is used to collect radioactive liquid waste, and exhausted bath box 300 passes through the first inlet 101 and first reactor 100 Connection.It is used to collect radioactive liquid waste by exhausted bath box 300, it is anti-radioactive liquid waste easily can be quantified into inflow first in batches Answer in device 100 and second reactor 200.Certainly, in other embodiments, exhausted bath box 300 can also omit, nuclear power station fortune The radioactive liquid waste produced during row can be flowed directly into first reactor 100 and handled.
In present embodiment, Spent Radioactive liquid processing device 10 includes first reactor 100 and second reactor 200, In other embodiments, Spent Radioactive liquid processing device 10 can also include the 3rd be connected in series with second reactor 200 Reactor, the 4th reactor etc..
Specifically, the flow diagram that first reactor 100 handles radioactive liquid waste is as shown in Figure 2.Spent Radioactive liquid stream After entering to be pre-loaded with the first reactor 100 of the first adsorbent, by the first blender 110 stir and evenly mix radioactive liquid waste with First adsorbent, mixes radioactive liquid waste and the first adsorbent.Adsorbent adsorbs the radionuclide in radioactive liquid waste, Radioactive liquid waste after processing, obtains the first supernatant and the first precipitation, the first supernatant in first reactor 100 after standing sedimentation Liquid is flowed into second reactor 200 by the first liquid outlet 103.After a period of time, as needed, the first precipitation is discharged Reactor, and supplement the first new adsorbent.
Specifically, Spent Radioactive liquid processing device 10 further includes solenoid valve, Spent Radioactive liquid processing device 10 1 is being used After the section time, first reactor 100 and 200 liquid of second reactor flow direction can also be exchanged by solenoid valve, make full use of suction Attached dose of adsorption capacity, on the premise of processing requirement is met, is reduced as far as radwaste yield.
Above-mentioned Spent Radioactive liquid processing device 10 is simple in structure, changes general use fixed bed reactors absorption mode, But radioactive liquid waste is mixed with adsorbent by stirring radioactive liquid waste, reacted by first reactor 100 and second After 200 two-stage adsorption treatment of device, radionuclide amount is few in the second obtained supernatant, meets discharge standard.Even glue Nucleic existing for figure, can also be handled, less energy consumption, the solid radiation of generation gives up by above-mentioned Spent Radioactive liquid processing device 10 Object amount is less.
In addition, referring to Fig. 3, the present invention also provides an embodiment treating apparatus for radioactive waste liquid 20, Spent Radioactive Liquid processing equipment 20 includes at least two above-mentioned Spent Radioactive liquid processing devices 10.In simultaneously between Spent Radioactive liquid processing device 10 Connection connection.
By the multiple Spent Radioactive liquid processing devices 10 being connected in parallel, a large amount of processing radioactive liquid wastes, place can be realized Reason amount is big, realizes the continuity processing of radioactive liquid waste.
Above-mentioned treating apparatus for radioactive waste liquid 20 is simple in structure, possesses that effective, selectivity is strong, miniaturization, modularization, removable The characteristics of property is strong is moved, it is low to the requirement of Site Service condition, it is complex and existing to be very suitable for nuclear power plant's radioactive liquid waste component The limited particular/special requirement of field arrangement space.Such as many links of nuclear industry can produce low radioactive waste liquid, some of which low radioactive waste liquid Generation is non-continuous, has dispersed feature in the time and space.Handled for these distributed low radioactive waste liquids, there is three Kind alternative plan:1) each spaced point establishes processing unit;2) waste liquid is transported to unified centrostigma from spaced point Handled;3) it is respectively processed using single or multiple wheeled apparatus to each spaced point.In each spaced point one by one It is big to build the investment for the treatment of facility, equipment vacancy rate is high, it is also necessary to put into substantial amounts of fund and safeguarded and retired, while also need It is equipped with and operator training, maintenance personnel and retiree, does not have economy.Low radioactive waste liquid is transported to system from spaced point One centralized processing point is handled, and freight volume is big, and freight is high, environmental risk caused by liquid radioactive waste transport Greatly, not permitted in regulation, without operability.The treating apparatus for radioactive waste liquid 20 of present embodiment is removable, according to Need to be moved to each spaced point and be respectively processed, can not only evade the risk in transit of liquid radioactive waste, but also can be to avoid Overlapping investment construction, improves utilization rate of equipment and installations, treating capacity is big, and energy consumption is small, and the radioactive solid waste amount of generation is less.
Referring to Fig. 4, the Spent Radioactive liquid processing method of an embodiment, includes the following steps S110~S160.
S110, provide Spent Radioactive liquid processing device or treating apparatus for radioactive waste liquid.
Specifically, the structure of Spent Radioactive liquid processing device is as shown in Figure 1, the structure such as figure for the treatment of apparatus for radioactive waste liquid Shown in 3.
S120, by radioactive liquid waste flow into first reactor in, by the first blender by radioactive liquid waste with first suction Attached dose stirs and evenly mixs, and the first adsorbent adsorbs the radionuclide in radioactive liquid waste.
Specifically, radioactive liquid waste can be low-activity waste liquid in being produced in nuclear power station operational process, the first reaction The first adsorbent is pre-loaded with device.Radioactive liquid waste can be flowed into first reactor by pipeline.
Specifically, the first adsorbent can be a kind of particle for being capable of Adsorption of Radioactive nucleic.In present embodiment, first The particle diameter of adsorbent is 10 μm~30 μm.After agitated, the first adsorbent can be suspended in radioactive liquid waste, thus with radiation Property waste liquid fully mix, adsorb waste liquid in radionuclide.For a period of time, the first adsorbent can settle standing sedimentation, real Existing separation of solid and liquid.
In present embodiment, the first adsorbent includes inorganic adsorbing material and the magnetic core being coated on inorganic adsorbing material Carrier Fe3O4
Inorganic adsorbing material, can putting from high salt amount to the high selectivity of main trace nucleic Cs, Sr, Co, Ag, I etc. Target species ion is efficiently removed in penetrating property waste liquid, the radioactive activity of waste liquid can quickly be greatly lowered, non-put is coexisted The influence of ion is smaller, therefore service life is grown, and quantity of solid waste is small.After the absorption of the first adsorbent, substantial amounts of radioactive nucleus Element is enriched in the first adsorbent of solid-state of small size, is easy to radiation protection.Compared to spent resin, what inorganic adsorbing material produced Radioactive waste heat endurance and chemical stability is good, radiation-resistant property is strong, is not easy, by RADIATION DECOMPOSITION or biological decomposition, to be easy to The processing disposal in later stage, during underground disposal head's phase stores, has more long-term safety.Coated on inorganic adsorbing material Magnetic core carrier Fe3O4, after the completion of stirring and adsorbing, the first adsorbent can quickly be settled by the principle of electromagnetic induction, into one Step improves treatment effeciency.
It will be appreciated, of course, that in other embodiments, the first adsorbent can not also have by magnetism, pass through gravity Also the first adsorbent can be settled.
After radioactive liquid waste is flowed into first reactor, radioactive liquid waste is stirred in the first reactor, makes radiation Property waste liquid and the first adsorbent mix, the first adsorbent by radioactive liquid waste radionuclide adsorb.By stirring operation, It can accelerate the first adsorbent to complete to adsorb in a short time with radioactive liquid waste, shorten the reaction time.
In present embodiment, change general use fixed bed reactors absorption mode, but by stirring Spent Radioactive Liquid mixes radioactive liquid waste and the first adsorbent.Specifically, radioactive liquid waste and first are adsorbed by the first blender In the operation that agent stirs and evenly mixs, stir speed (S.S.) is 250rpm~350rpm, and mixing time is 2min~3min.The results showed 2min~3min is stirred, removal rate i.e. reachable more than 99% of radionuclide, treatment effeciency significantly improves, and suitable treatment is dashed forward A large amount of radioactive liquid wastes that hair event produces.
The first supernatant and the first precipitation are obtained after S130, standing sedimentation.
After the completion of radioactive liquid waste and the first adsorbent adsorption reaction, a period of time is stood, realizes separation of solid and liquid so as to obtain Precipitated to the first supernatant and first.First supernatant further can be flowed into flow into equipped with the second adsorbent the by pipeline Handled in two reactors.And the radioactive liquid waste of next batch can be again flowed into first reactor, the first adsorbent without Need to take out, repeat the multiple batches of radioactive liquid waste of processing, until the first adsorbent reaches saturation, then mended into first reactor Fill the first new adsorbent.
Specifically, being obtained after standing sedimentation in the first supernatant and the first operation precipitated, the standing sedimentation time is 2min ~3min.The results showed preferable separation of solid and liquid can be achieved in standing sedimentation 2min~3min.Most of radionuclide with First adsorbent settles to form the first precipitation.Compared to ion-exchange process, present embodiment is promoted by the way of stirring and evenly mixing First adsorbent and radioactive liquid waste adsorption reaction, realize separation of solid and liquid, the first adsorbent by the way of standing sedimentation afterwards The multiple batches of radioactive liquid waste of repeatable processing, the radioactive solid waste amount of generation are less.
S140, by the first supernatant liquid stream second reactor obtained in S130, by the second blender by the first supernatant Liquid is stirred and evenly mixed with the second adsorbent, and the second adsorbent adsorbs the radionuclide in the first supernatant.
After the first supernatant and the first precipitation are obtained after standing sedimentation, the first supernatant is flowed into equipped with the second adsorbent Second reactor in be further processed.Specifically, the first supernatant can be flowed into second reactor by pipeline.
Specifically, the second adsorbent can be a kind of particle for being capable of Adsorption of Radioactive nucleic.In present embodiment, second The particle diameter of adsorbent is 10 μm~30 μm.After agitated, the second adsorbent can be suspended in the first supernatant, so that with first Supernatant fully mixes, and adsorbs the radionuclide in the first supernatant.For a period of time, the second adsorbent can sink standing sedimentation Drop, realizes separation of solid and liquid.
In present embodiment, the second adsorbent includes inorganic adsorbing material and the magnetic core being coated on inorganic adsorbing material Carrier Fe3O4.Inorganic adsorbing material, can putting from high salt amount to the high selectivity of main trace nucleic Cs, Sr, Co, Ag, I etc. Target species ion is efficiently removed in penetrating property waste liquid, the radioactive activity of waste liquid can quickly be greatly lowered, non-put is coexisted The influence of ion is smaller, therefore service life is grown, and quantity of solid waste is small.After the absorption of the second adsorbent, radionuclide enrichment In the second adsorbent of solid-state of small size, it is easy to radiation protection.Magnetic core carrier Fe is coated on inorganic adsorbing material3O4, when stirring After the completion of mixing absorption, the second adsorbent can quickly be settled by the principle of electromagnetic induction, further improve treatment effeciency.
It will be appreciated, of course, that in other embodiments, the second adsorbent can not also have by magnetism, pass through gravity Also the second adsorbent can be settled.
Specifically, the first adsorbent is identical with the second sorbent material, and after the absorption of two-stage sequencing batch type, Spent Radioactive Radionuclide in liquid is adsorbed by the first adsorbent and the second adsorbent substantially, so as to reach discharge standard.First absorption Agent and the second adsorbent can repeatedly use, and without taking out after single treatment, reduce radioactive solid waste amount.
After first supernatant is flowed into second reactor, the first supernatant is stirred in the second reactor, makes first Supernatant and the second adsorbent mix, and the second adsorbent adsorbs remaining radionuclide in the first supernatant.Pass through stirring Operation, can accelerate the second adsorbent and complete to adsorb in a short time with the first supernatant, shorten the reaction time.
Specifically, being stirred and evenly mixed the first supernatant and the second adsorbent by the second blender, stir speed (S.S.) is 250rpm~350rpm, mixing time are 2min~3min.Second adsorbent, which repeats, handles the first multiple batches of supernatant.
The second supernatant and the second precipitation are obtained after S150, standing sedimentation.
After the completion of first supernatant and the second adsorbent adsorption reaction, a period of time is stood, realizes separation of solid and liquid so as to obtain Precipitated to the second supernatant and second.When the second supernatant meets discharge standard, the second supernatant is discharged into second reactor. The first supernatant of next batch can be again flowed into second reactor, repeats the first multiple batches of supernatant of processing, until Second adsorbent reaches saturation, then the second new adsorbent is supplemented into second reactor.
Specifically, being obtained after standing sedimentation in the second supernatant and the second operation precipitated, the standing sedimentation time is 2min ~3min.The results showed preferable separation of solid and liquid can be achieved in standing sedimentation 2min~3min.It is remaining in first supernatant Radionuclide settles to form the second precipitation with the second adsorbent.Without taking out after the second adsorbent after sedimentation, the second adsorbent The first multiple batches of supernatant of repeatable processing, until the second adsorbent reaches saturation, then is supplemented newly into second reactor Second adsorbent, the radioactive solid waste amount of generation are less.
S160, when the second supernatant meets discharge standard, by the second supernatant discharge second reactor.
Specifically, after first reactor and the adsorption treatment of second reactor two-stage sequencing batch type, in detection second Whether the radionuclide in clear liquid meets discharge standard, and when the second supernatant meets discharge standard, the second supernatant is arranged Go out second reactor, the radioactive liquid waste processing of the batch is completed.
If the second supernatant is not up to discharge standard, the second supernatant further can be flowed into what is be connected with second reactor 3rd reactor, the 4th reactor being connected with the 3rd reactor ... handled, until discharge supernatant reach discharge Standard.
In present embodiment, radioactive liquid waste is flowed into before the operation in the first reactor equipped with the first adsorbent, The operation for collecting radioactive liquid waste is further included, flows into the radioactive liquid waste of collection equipped with the first absorption by way of in batches In the first reactor of agent, after operation in the second reactor that the first supernatant flows into equipped with the second adsorbent, to the The radioactive liquid waste of next batch is flowed into one reactor.Handle in batches, realize the continuity processing of radioactive liquid waste processing.
Specifically, can be as needed, the amount of the radioactive liquid waste of distribution every batch of processing.Specifically, the first adsorbent with The solid-to-liquid ratio of radioactive liquid waste is 20g/L~60g/L.Effective volume in first reactor per 1L, corresponding input 20g~ The first adsorbent of 60g.The influx of second adsorbent is 20g/L~60g/L.Effective volume in second reactor per 1L, The second adsorbent of corresponding input 20g~60g.Show through result of the test, the first adsorbent and the are put into by above-mentioned dosage Two adsorbents, good adsorption capacity, the first adsorbent and second are kept after can handling the radioactive liquid waste of more than 70 batches Adsorbent is reused, and effectively reduces the radioactive solid waste amount produced.
In present embodiment, Spent Radioactive liquid processing method is additionally included in using Spent Radioactive liquid processing device or radioactivity Waste liquor treatment equipment for a period of time after, replace first reactor in the first adsorbent, by first reactor with second reaction Liquid flow direction in device is exchanged, and this method comprises the following steps afterwards:Radioactive liquid waste is flowed into second reactor, by the Two blenders stir and evenly mix radioactive liquid waste and the second adsorbent, and the second adsorbent is by the radionuclide in radioactive liquid waste Adsorb, the 3rd supernatant and the 3rd precipitation are obtained after standing sedimentation.3rd supernatant is flowed into first reactor.Pass through first First adsorbent of the blender by the 3rd supernatant and after replacing stirs and evenly mixs, and the first adsorbent after replacement is by the 3rd supernatant Radionuclide absorption in liquid.The 4th supernatant and the 4th precipitation are obtained after standing sedimentation.When the 4th supernatant meets discharge During standard, the 4th supernatant is discharged into first reactor.
Since the radionuclide concentration level of the radioactive liquid waste handled in first reactor is higher, the first reaction There is failure state first in the first adsorbent in device, and the second adsorbent in second reactor also has good suction at this time Attached activity.At this time, the operation of discharge adsorbent can be only carried out to first reactor, and loads the first new adsorbent, and the The second adsorbent in two reactors is changed without.Then first reactor and second reactor liquid flow direction are exchanged, i.e., it is original First reactor and second reactor backward operation.Radioactive liquid waste is flowed into the second reactor equipped with the second adsorbent In.By the way that first reactor and second reactor liquid flow direction are exchanged, the second adsorbent in second reactor can repeat It is used for multiple times, and first adsorbent of the water exit end always in first reactor is new adsorbent, ensures the purification requirement of water outlet. Specifically, the switching of the processing sequence of first reactor and second reactor relies on solenoid valve control.Present embodiment can fill Divide the adsorption capacity using adsorbent, on the premise of processing requirement is met, be reduced as far as radwaste yield.
Above-mentioned Spent Radioactive liquid processing method obtains after first reactor and second reactor two-stage adsorption treatment The second supernatant in radionuclide amount it is few, meet discharge standard., also can be by first even nucleic existing for colloidal attitude Adsorbent or the absorption of the second adsorbent, so that precipitated during standing sedimentation, therefore radioactive liquid waste can directly carry out two Level adsorption treatment, can save the operation of evaporation process, and energy consumption is small.First adsorbent and the second adsorbent, which can be repeated several times, to be made With treating capacity is big, and the radioactive solid waste amount of generation is less.
It is specific embodiment part below.
In following embodiments, the radionuclide in radioactive liquid waste is Cs+, the first adsorbent and the second adsorbent phase What is answered is that can adsorb Cs+Adsorbent.The method is conventional method, the raw material and detection institute unless otherwise instructed It can be obtained unless otherwise instructed from open commercial sources with standardizing chemical reagent.
In all of the embodiments illustrated, Cs before and after absorption+The concentration using plasma mass spectrum (ICP-MS) of ion measures. Performance of the adsorbent uses Cs+The removal rate of ion represents.Removal rate RRt(%) as shown in following formula 1,
Wherein, RRtFor Cs (I) removal rate of t moment, C0For raw water Cs+Concentration (mg/L), CtFor t moment solution C s+Concentration (mg/L)。
Embodiment 1
The micron order magnetic core cladded type ferrocyanide that the adsorbent selected in the present embodiment is voluntarily developed removes caesium adsorbent (Chinese invention patent ZL201210347269.8).Adsorbent is tested to target species Cs+Removal capacity.Respectively in reactor The interior adsorbent for flowing into 20g/L, 40g/L and 60g/L carries out batch experiment, and research adsorbent is to Cs in solution+Absorption situation. Radioactive liquid waste uses CsNO3Tap water (about 980 μ s/cm of electrical conductivity, 550~750mg/L of corresponding salinity) is dissolved in prepare, Cs+ Concentration is 1.5mg/L.Within the 13min that reaction is stirred under the conditions of 300rpm, specific point in time sampling (sample volume is chosen The ratio for accounting for overall solution volume is small to ignoring), and analyze wherein Cs+Concentration, Cs (I) is calculated by above formula (1) Removal rate.Removal rate under the conditions of the dosage of different adsorbents maps t, as shown in Figure 5.Result of the test is visible:Inhale Attached dose of dosage is bigger, faster to the removal speed of Cs (I).Under the conditions of each dosage, most of Cs+Gone in 2min Remove.Specifically in 2min, 3min and 5min to Cs+Removal rate data such as table 1 below.
Table 1:Adsorbent is under different dosages to the removal rate (%) of Cs (I)
Data above surface, in 2min, Cs when dosage is 20g/L+Removal rate removal rate when being 99.3%, 40g/L For 99.6%, 60g/L when removal rate up to 99.9%, be hereafter further added by the reaction time, removal rate no longer substantially increases.Thus may be used See, stirring and adsorbing reaction time 2min or so, adsorbent can adsorb the radionuclide in radioactive liquid waste.
Embodiment 2
The adsorbent selected in the present embodiment is the micron order magnetic core cladded type ferrocyanide voluntarily developed except caesium adsorbs Agent (Chinese invention patent ZL201210347269.8).Experiment determines the gravitational settling time with verification adsorbent.
Caesium adsorbent is removed to magnetism selected in this present embodiment, we also test carries out Magneto separate using externally-applied magnetic field The experiment of sedimentation.In experiment, electric circle is wound in reactor outer wall, externally-applied magnetic field can be both produced after energization, adsorbent was at several seconds Among can just be attracted on completely on reactor wall, complete the quick separating of solid liquid phase.In view of in nuclear power station actual motion, Simplify structure design and the operation of reactor as far as possible, therefore by taking this magnetic adsorbent as an example, the high spot reviews gravity of adsorbent Settling property.
The free settling process of individual particle in media as well can be divided into boost phase and constant velocity stage.For little particle Speech, boost phase is usually extremely short, can ignore.Then, it is at the uniform velocity process that whole infall process, which can be assumed that,.
Stokes sedimentation formula (2) described sinking speed is the final speed of infall process, i.e. constant velocity stage Sinking speed u0It can be calculated and obtained by following formula:
Wherein, g is acceleration of gravity, and r is particle radius, and ρ is grain density, and ρ ' is the density of liquid medium, and η is liquid The viscosity of medium.
The size distribution situation of the adsorbent in the present embodiment is measured using laser particle size analyzer, as shown in Figure 6.Grain For footpath substrate between 10 μm~30 μm, median is 23.35 μm.
Measure the density of adsorbent is about 4.0g/mL, the density of aqueous is 1.0g/mL, viscosity 0.001Pa S, then the particle sinking speed calculated according to Stokes sedimentation formula is 3.56mm/s.For being applicable in for proof theory sinking speed Property, the graduated cylinder of 500mL is selected, diameter about 5cm, high about 25cm carry out sedimentation experiment, test process photo referring to attached drawing 7.Design In theoretical sinking speed 3.56mm/s can be used as reference, then theoretical sinking speed calculate needed for the sedimentation time be 1.17min. Experimental result shows that solution is clarified completely in 1min to 2min, illustrates that use meets preferably with actual result.Above-mentioned sedimentation The research of speed shows, it is not necessary to which, by externally-applied magnetic field, adsorbent can just realize preferable separation of solid and liquid in 2min.Therefore can Remove externally-applied magnetic field, system can be made more simple and reliable, reduce running control and operation.
Embodiment 3
The micron order magnetic core cladded type that the first adsorbent and the second adsorbent selected in the present embodiment are voluntarily developed is sub- The iron cyanide removes caesium adsorbent (Chinese invention patent ZL201210347269.8).Two-stage sequencing batch type reactor is employed, is tested It is to Cs+Removal capacity.In laboratory conditions, using Spent Radioactive liquid processing device (two-stage sequencing batch type as shown in Figure 1 Reactor) carry out batch experiment.Wherein radioactive liquid waste uses CsNO3It is dissolved in tap water (about 980 μ s/cm of electrical conductivity, corresponding salt 550~750mg/L of concentration) prepare, Cs+Concentration is 1.5mg/L, and the effective volume of first reactor and second reactor is 1L.The first adsorbent and the quality that adds of the second adsorbent flowed into first reactor and second reactor be 40g, is 1L per batch processing water.In experiment, radioactive liquid waste initially enters first reactor, anti-under 300rpm mixing speeds 2.5min, standing sedimentation 2.5min is answered to obtain the first supernatant and the first precipitation.The first supernatant samples of part are taken to carry out Cs+It is dense Degree detection and the first supernatant, which flow into, to be equipped with the second reactor of the second adsorbent.Stirred in the second reactor with 300rpm After reacting 2.5min, standing sedimentation 2.5min under speed, the second supernatant and the second precipitation are obtained.Take part the second supernatant sample Product carry out Cs+Concentration Testing, when the second supernatant meets discharge standard, second reactor is discharged by the second supernatant.When One supernatant is flowed into after the operation in the second reactor equipped with the second adsorbent, and next batch is flowed into first reactor Radioactive liquid waste.So move in circles.Use the primary effluent sample (the first supernatant samples) of ICP-MS measurement each batches With the Cs in secondary effluent sample (the second supernatant samples)+Concentration, and calculate decontamination factor DF according to (3) formula:
Wherein, CinTo enter the water inlet Cs of corresponding reactor+Concentration (mg/L), CoutFor corresponding reactor Water outlet Cs+Concentration (mg/L), DF are decontamination factor.
After tested, the decontamination factor of first reactor, the decontamination factor of second reactor and first reactor and second For the decontamination factor of reactor totality with the situation of change of processing batch as shown in figure 8, abscissa is processing batch, ordinate is to go The logarithm of the dirty factor, it is similar in the figure of following decontamination factor.Specifically, aqueous concentration (the first supernatant C s of first reactor+ Concentration) and second reactor aqueous concentration (the second supernatant C s+Concentration) with situation of change such as Fig. 9 institutes of processing batch Show.The Cs of single batch in first reactor and second reactor+The situation of change of adsorbance is as shown in Figure 10.First reactor And the Cs added up in second reactor+Adsorbance situation of change is as shown in figure 11.
It can be seen from the results above that Spent Radioactive liquid processing method through this embodiment handles 70 batches (70L) After radioactive liquid waste, the decontamination factor of first reactor and second reactor totality is still higher, has good dirt-removing power. In the starting stage, the decontamination factor of first reactor is more than 1000.With processing batch increase, the primary effluent of first reactor Concentration gradually increases, and first order decontamination factor is gradually reduced.Since primary effluent concentration increases, the effect that second reactor plays More and more obvious, the decontamination factor of second reactor increases with the increase of processing batch.The overall removal of soils of two-stage reactor because Son remains to be remained above 1000 after 70 batches of radioactive wastewaters are handled.
In nuclear industry, processing need to be passed through and store for a long time by being enriched the discarded adsorbent of radionuclide, therefore be radiated The volume of property waste should small quantization.After tested in the present embodiment, under conditions of meeting that decontamination factor is more than 1000, processing What the radioactive wastewater of 70L produced discards adsorbent only 40g (about 10mL), treating capacity and waste yield volume ratio containing Cs (I) For 7000.Two-stage sequencing batch type liquid waste treating apparatus can make full use of the adsorption capacity of adsorbent, before processing requirement is met Put, be reduced as far as radwaste yield.
Embodiment 4
In the present embodiment, radioactive liquid waste is first handled using the method for embodiment 3, when the decontamination factor of first reactor subtracts It is small to a certain extent when (being, for example, less than 1000) when, it is meant that the adsorbent in reactor will exhaust, pass through be filtered by vacuum dress Put and discharge the first adsorbent, load the first new adsorbent in the first reactor, and second in second reactor is adsorbed Agent is changed without.Then first reactor and the liquid flow direction in second reactor are exchanged, the first of the first adsorbent will be updated Reactor is used as the second level in ensuing processing procedure, and using second reactor (the second stage reactor before) as Level-one uses, and to improve adsorbent utilization rate, ensures outlet effect, reduces radwaste yield.
Embodiment 5
The micron order magnetic core cladded type that the first adsorbent and the second adsorbent selected in the present embodiment are voluntarily developed is sub- The iron cyanide removes caesium adsorbent (Chinese invention patent ZL201210347269.8).According to the two-stage reactor examination in embodiment 3 Test as a result, devising treating apparatus for radioactive waste liquid as shown in Figure 3.The treating apparatus for radioactive waste liquid include two it is in parallel Liquid waste treating apparatus.The mode of two-way parallel connection is taken to run, the height for setting single reactor is 45cm, and basal diameter is 50cm, per reactor effective volume about 85L single all the way.After tested, in the case where ensureing that the overall removal of soils factor is more than 1000, The treatment scale of the equipment is set to reach 1t/h (ton hour).Treating apparatus for radioactive waste liquid operation can be divided into four-stage, respectively To intake, adsorbing, precipitating, water outlet.Cs in waste liquid+Concentration for 1.5mg/L, water inlet, absorption, precipitation, water outlet stage are each 2.5min.One batch processed needs 10min, can handle 6 batches per hour.
It is 40g/L that adsorbent, which adds solid-to-liquid ratio, i.e., each reactor adsorbent adds quality about 3400g.The two-way is in parallel The operational mode of two-stage reactor is:Intake, adsorb in operation, precipitation, each 2.5min of water outlet stage.When 1-A reactors are in During the water outlet stage of a cycle, 1-B initially enters the fill phase of a cycle;Subsequent 2.5min, 1-A are water inlet rank Section, 1-B is absorption phase;2.5min afterwards, 1-A are absorption phase, and 1-B is precipitate phase;Ensuing 2.5min, 1-A are Precipitate phase, 1-B are water outlet stage;When 1-A enters the water outlet stage of second round, 1-B is just into second period Fill phase.The linked manner of 2-A and 2-B reactors is also such.And so on circulate, until water outlet Cs+Concentration does not reach Untill it is required that.
Test method test decontamination factor in embodiment 3.(the water outlet Cs when the overall removal of soils factor is 1000+It is dense When degree reaches the one thousandth of influent concentration), whole equipment runs about 70 circulations, and the amount of disposing waste liquid about 11900L, produces useless Abandon adsorbent about 6.8kg (about 1.7L), treating capacity and waste yield volume ratio about 7000.The treating capacity of the equipment is big, processing Efficient, radwaste yield is small.
Embodiment 6
The effect of enhanced processing amount on the Spent Radioactive liquid processing method processing plant production line of the present embodiment test present invention Fruit.First adsorbent and the second adsorbent are magnetic core cladded type ferrocyanide except caesium adsorbent (passes through Chinese invention patent Prepared after the method industry extension production of ZL201210347269.8), it prepares the first adsorbent and the second adsorbent is adopted Magnetic core is the industrial magnetic powder of 100 mesh.Using Spent Radioactive liquid processing device 10 as shown in Figure 1, (two-stage sequencing batch type reacts Device) carry out batch experiment.Each reactor dischargeable capacity is 20L, and every batch of processing water is 20L.Devised in reactor certainly Dynamic control, switches over a two level, and water inlet and draining are automatically stopped by Liquid level after set batch number is completed Operation.The disposition of two groups of difference adsorbent dosages is tested respectively.Adsorbent dosage in each reactor in first group For 40g/L, it is 3min to control stirring and adsorbing reaction time and standing sedimentation time.Adsorbent in each reactor in second group Dosage is 60g/L, and it is 3min to control stirring and adsorbing reaction time and standing sedimentation time.First group of experiment is thrown when adsorbent When dosage is 40g/L, the decontamination factor of first reactor, the decontamination factor of second reactor and first reactor and second anti- Answer the decontamination factor of device totality as shown in figure 12 with the situation of change of processing batch.It can be recognized from fig. 12 that with processing batch Increase, the decontamination factor of first reactor is gradually reduced, and the decontamination factor of second reactor gradually increases, first reactor and The overall removal of soils factor of second reactor totality slowly reduces, and decontamination factor is reduced to after about 30 batch raw waters are handled 1000, handle about 70 batch raw waters and be reduced to 100 afterwards.If it is required that decontamination factor be more than 1000, then by processing 30 Batch calculates, the enrichment Cs that processing 600L raw waters produce+Discarded adsorbent be 800g, treating capacity and the volume of waste yield Than for 3000.Under conditions of meeting that decontamination factor is more than 100, respective volume ratio is 7000.Illustrate that the method for the present invention is expanding In big industrial production practical application, treatment effeciency is still higher, and radwaste yield is small.
If Figure 13 is the decontamination factor of first reactor and second reactor totality in first group of experiment and second group of experiment With the situation of change of processing batch.It can be seen that from Figure 13 results when adsorbent dosage brings up to 60g/L from 40g/L, React incipient stage Cs+Decontamination factor be obviously improved, under conditions of meeting decontamination factor 1000, can will processing batch be carried from 30 It is high to 70 batches.As it can be seen that adsorbent dosage improves 50%, decontamination factor handles batch raising more than 1000 for experiment One times.As it can be seen that adsorbent dosage is brought up to 60g/L from 40g/L from experiment, had no significant effect to stirring, settling etc.. Therefore the balance of detersive efficiency and quantity of solid waste should be considered, with preferably suitable adsorbent dosage.Second group of experiment In, meet that decontamination factor can handle 70 batches under conditions of being 1000, that is, handle 1400 liters of waste water, produce solid waste 1200 Gram, wastewater treatment capacity and waste yield volume ratio are 4600, illustrate that the method for the present invention is answered widened industrial production is actual In, treatment effeciency is still higher, and radwaste yield is small.
Embodiment described above only expresses the several embodiments of the present invention, its description is more specific and detailed, but simultaneously Therefore the limitation to the scope of the claims of the present invention cannot be interpreted as.It should be pointed out that for those of ordinary skill in the art For, without departing from the inventive concept of the premise, various modifications and improvements can be made, these belong to the guarantor of the present invention Protect scope.Therefore, the protection domain of patent of the present invention should be determined by the appended claims.

Claims (8)

1. a kind of Spent Radioactive liquid processing method, it is characterised in that include the following steps:
Spent Radioactive liquid processing device or treating apparatus for radioactive waste liquid are provided, wherein, the Spent Radioactive liquid processing device bag First reactor and second reactor are included, is equipped with the first blender in the first reactor, the first reactor is equipped with First inlet and the first liquid outlet, first inlet are used to flow into radioactive liquid waste in the first reactor, make Used time loads the first adsorbent in the first reactor, and first blender is used to stir and evenly mix the radioactive liquid waste With first adsorbent, the second reactor is interior to be equipped with the second blender, and the second reactor is equipped with the second feed liquor Mouth and the second liquid outlet, second inlet are connected with first liquid outlet by pipeline, and second inlet is used for The first supernatant for being formed after first reactor processing is flowed into the second reactor, when use is anti-described second Answer and load the second adsorbent in device, second blender is used to stir and evenly mix first supernatant and the described second absorption Agent, second liquid outlet are used for the second supernatant discharge second reaction that will be formed after second reactor processing Device, the treating apparatus for radioactive waste liquid include at least two Spent Radioactive liquid processing devices, at the radioactive liquid waste It is in be connected in parallel between reason device;Radioactive liquid waste is flowed into the first reactor, by first blender by institute State radioactive liquid waste to stir and evenly mix with first adsorbent, first adsorbent is by the radioactivity in the radioactive liquid waste Nucleic adsorbs;
The first supernatant and the first precipitation are obtained after standing sedimentation;
First supernatant is flowed into the second reactor, by second blender will first supernatant and Second adsorbent stirs and evenly mixs, and second adsorbent adsorbs the radionuclide in first supernatant;
The second supernatant and the second precipitation are obtained after standing sedimentation;And
When second supernatant meets discharge standard, second supernatant is discharged into the second reactor.
2. Spent Radioactive liquid processing method according to claim 1, it is characterised in that described that radioactive liquid waste is flowed into institute Before stating the operation in first reactor, the operation for collecting radioactive liquid waste is further included, will be received by way of in batches afterwards The radioactive liquid waste of collection is flowed into the first reactor, when first supernatant is flowed into the second reactor After operation, the radioactive liquid waste of next batch is flowed into the first reactor.
3. Spent Radioactive liquid processing method according to claim 1, it is characterised in that first adsorbent is put with described The solid-to-liquid ratio of penetrating property waste liquid is 20g/L~60g/L, and the solid-to-liquid ratio of second adsorbent and first supernatant is 20g/L ~60g/L.
4. Spent Radioactive liquid processing method according to claim 1, it is characterised in that the method is additionally included in using institute After stating Spent Radioactive liquid processing device or the treating apparatus for radioactive waste liquid for a period of time, replace in the first reactor First adsorbent, and the liquid flow direction of the first reactor and the second reactor is exchanged, afterwards the side Method includes the following steps:
The radioactive liquid waste is flowed into the second reactor, by second blender by the radioactive liquid waste with Second adsorbent stirs and evenly mixs, and second adsorbent adsorbs the radionuclide in the radioactive liquid waste;
The 3rd supernatant and the 3rd precipitation are obtained after standing sedimentation;
3rd supernatant is flowed into the first reactor, by first blender by the 3rd supernatant with And first adsorbent after replacing stirs and evenly mixs, first adsorbent after replacement is by putting in the 3rd supernatant Penetrating property nucleic adsorbs;
The 4th supernatant and the 4th precipitation are obtained after standing sedimentation;And
When the 4th supernatant meets discharge standard, the 4th supernatant is discharged into the first reactor.
5. Spent Radioactive liquid processing method according to claim 1, it is characterised in that described to pass through first blender In the operation that the radioactive liquid waste and first adsorbent are stirred and evenly mixed, stir speed (S.S.) is 250rpm~350rpm, Mixing time is 2min~3min;In the operation that the first supernatant and the first precipitation are obtained after the standing sedimentation, standing sedimentation Time is 2min~3min.
6. Spent Radioactive liquid processing method according to claim 1, it is characterised in that described to pass through second blender In the operation that first supernatant and second adsorbent are stirred and evenly mixed, stir speed (S.S.) is 250rpm~350rpm, is stirred It is 2min~3min to mix the time;In the operation that the second supernatant and the second precipitation are obtained after the standing sedimentation, during standing sedimentation Between be 2min~3min.
7. Spent Radioactive liquid processing method according to claim 1, it is characterised in that first adsorbent includes inorganic Sorbing material and the magnetic core carrier Fe being coated on the inorganic adsorbing material3O4;Second adsorbent includes inorganic adsorbent Material and the magnetic core carrier Fe3O4 being coated on the inorganic adsorbing material.
8. Spent Radioactive liquid processing method according to claim 1, it is characterised in that the particle diameter of first adsorbent is 10 μm~30 μm, the particle diameter of second adsorbent is 10 μm~30 μm.
CN201611207471.5A 2016-12-23 2016-12-23 Spent Radioactive liquid processing method, Spent Radioactive liquid processing device and equipment Active CN106683731B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201611207471.5A CN106683731B (en) 2016-12-23 2016-12-23 Spent Radioactive liquid processing method, Spent Radioactive liquid processing device and equipment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201611207471.5A CN106683731B (en) 2016-12-23 2016-12-23 Spent Radioactive liquid processing method, Spent Radioactive liquid processing device and equipment

Publications (2)

Publication Number Publication Date
CN106683731A CN106683731A (en) 2017-05-17
CN106683731B true CN106683731B (en) 2018-05-15

Family

ID=58871452

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201611207471.5A Active CN106683731B (en) 2016-12-23 2016-12-23 Spent Radioactive liquid processing method, Spent Radioactive liquid processing device and equipment

Country Status (1)

Country Link
CN (1) CN106683731B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107993734B (en) * 2017-12-01 2021-07-06 天津大学 Method for treating water polluted by radioactive iodide ions
WO2019203725A1 (en) * 2018-04-17 2019-10-24 E.L.I (Environment Laboratory Impact) Services Pte. Ltd. Process and system for removing radioactive ions present in a liquid
CN110467179A (en) * 2018-05-09 2019-11-19 上海核工程研究设计院有限公司 A method of active carbon is handled with nuclear facilities radioactive liquid waste chemical flocculation
CN109754887A (en) * 2018-12-24 2019-05-14 江苏核电有限公司 The method and its system of the processing of nuclear power station radioactive liquid waste are carried out using adsorbent material
CN109754888A (en) * 2019-01-16 2019-05-14 中国辐射防护研究院 A method of radioactivity waste oil is handled using spent sorbents in nuclear power station

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105161154A (en) * 2015-08-27 2015-12-16 中核四川环保工程有限责任公司 Simulated low-emission organic waste liquid pyrolysis incineration suspending liquid formula and preparation method thereof
CN105355250A (en) * 2015-10-16 2016-02-24 华东理工大学 Method for treating nuclear power plant radioactive waste liquid based on birnessite in-situ reaction
CN205595081U (en) * 2016-05-17 2016-09-21 中电投远达环保工程有限公司重庆科技分公司 Low waste water treatment experimental system of putting based on flocculation and precipitation method
CN205751546U (en) * 2016-05-17 2016-11-30 南华大学 The up-flow anaerobic biofilter processed for acid uranium-containing waste water

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4196551B2 (en) * 2001-08-16 2008-12-17 栗田エンジニアリング株式会社 Decontamination method and decontamination agent

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105161154A (en) * 2015-08-27 2015-12-16 中核四川环保工程有限责任公司 Simulated low-emission organic waste liquid pyrolysis incineration suspending liquid formula and preparation method thereof
CN105355250A (en) * 2015-10-16 2016-02-24 华东理工大学 Method for treating nuclear power plant radioactive waste liquid based on birnessite in-situ reaction
CN205595081U (en) * 2016-05-17 2016-09-21 中电投远达环保工程有限公司重庆科技分公司 Low waste water treatment experimental system of putting based on flocculation and precipitation method
CN205751546U (en) * 2016-05-17 2016-11-30 南华大学 The up-flow anaerobic biofilter processed for acid uranium-containing waste water

Also Published As

Publication number Publication date
CN106683731A (en) 2017-05-17

Similar Documents

Publication Publication Date Title
CN106683731B (en) Spent Radioactive liquid processing method, Spent Radioactive liquid processing device and equipment
RU2529018C2 (en) Method of deactivating liquid effluent, containing one or more radioactive chemical elements, by processing in fluidised bed
Chen et al. An overview on membrane strategies for rare earths extraction and separation
Ambashta et al. Water purification using magnetic assistance: a review
TWI576859B (en) A radioactive waste treatment method and a radioactive waste liquid treatment apparatus
JP5947271B2 (en) Decontamination system
Zhang et al. Enhanced removal of iodide ions by nano Cu2O/Cu modified activated carbon from simulated wastewater with improved countercurrent two-stage adsorption
Luo et al. Research on a pellet co-precipitation micro-filtration process for the treatment of liquid waste containing strontium
Rahman et al. Overview on recent trends and developments in radioactive liquid waste treatment part 1: sorption/ion exchange technique
KR20170101962A (en) Treatment of Liquid Radioactive Waste and Method for its Recovery
Liu et al. Removal of radioactive iodide from simulated liquid waste in an integrated precipitation reactor and membrane separator (PR-MS) system
CN110349689B (en) Radioactive waste liquid treatment device for nuclear power station
Yong et al. Treatment of the wastewater containing low-level 241Am using flocculation-microfiltration process
CN101500949A (en) Method and device for eliminating foreign matters present in dissolved form from waste water
JP2012232253A (en) Multistage seawater purification system
CN104478117A (en) Heavy-metal-containing wastewater treatment and recovery method and device
CN106241974A (en) Equipment for treating water from mine and method for treating water
CN110379532B (en) Method and device for treating radioactive waste liquid
Yoshizuka et al. Arsenic and boron in geothermal water and their removal
US20220055927A1 (en) Desalination of water using a complexing agent attached to a magnetic nanoparticle
JP2007222712A (en) Method and apparatus for separating and removing radioactive element by magnetic separation
JP2005262046A (en) Magnetic separation device and water-cleaning device using it
CN209312447U (en) A kind of decontamination waste liquid near-zero release processing unit of uranium-bearing and detergent
CN109411106B (en) Near-zero emission treatment device and treatment method for decontaminating waste liquid containing uranium and detergent
Han et al. Laboratory-scale studies on the removal of cesium with a submerged membrane adsorption reactor

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant